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+BioMedGraphica_Conn_ID,BioMedGraphica_ID,SNOMEDCT_ID,UMLS_Name,MeSH_Name,ICD11_ID,ICD11_Title,ICD10_ID,DO_ID,DO_Name,UMLS_ID,MeSH_ID,OMIM_ID,MONDO_ID,MONDO_Name,SNOMEDCT_Name
+BMGC_DS00001,BMG_DS000001,83123000;190787008,Abetalipoproteinemia,Abetalipoproteinemia,5C81.Z,"Hypolipoproteinaemia, unspecified",E78.6,DOID:1386,abetalipoproteinemia,C0000744,D000012,MTHU014871;200100,MONDO:0008692,abetalipoproteinemia,Abetalipoproteinemia | Abetalipoproteinaemia | Abetalipoproteinemia (disorder) | ABL - Abetalipoproteinaemia | Abetalipoproteinaemia | Apolipoprotein B deficiency | Abetalipoproteinemia | ABL - Abetalipoproteinemia | Abetalipoproteinemia (disorder) | Bassen-Kornzweig disease | Homozygous familial hypobetalipoproteinaemia | Homozygous familial hypobetalipoproteinemia
+BMGC_DS00002,BMG_DS000002,47344007,Abnormality of secretion of gastrin,,,,,DOID:13656,gastrin secretion abnormality,C0000774,,,MONDO:0001770,gastrin secretion abnormality,Abnormality of secretion of gastrin | Abnormality of secretion of gastrin (finding)
+BMGC_DS00003,BMG_DS000003,,"Abortion, Habitual","Abortion, Habitual",,,,,,C0000809,D000026,,MONDO:0006774,habitual spontaneous abortion,
+BMGC_DS00004,BMG_DS000004,267187007;198616002;156087000;16607004,Missed abortion,,JA03,Missed abortion,O02.1,,,C0000814,,,,,Missed abortion | Missed abortion (disorder) | Missed abortion | Missed abortion (disorder) | MA - Missed abortion | Silent miscarriage | Missed miscarriage
+BMGC_DS00005,BMG_DS000005,,,,,,,DOID:9667,placental abruption,C0000821,,,,,
+BMGC_DS00006,BMG_DS000006,,"Abortion, Veterinary","Abortion, Veterinary",,,,,,C0000823,D000034,,,,
+BMGC_DS00007,BMG_DS000007,,,,,,,,,C0000832,,,MONDO:0004846,placental abruption,
+BMGC_DS00008,BMG_DS000008,44132006;128477000,Abscess,Abscess,,,,,,C0000833,D000038,,MONDO:0005227,abscess,Abscess | Abscess (morphologic abnormality) | Abscess morphology | Abscess (disorder) | Abscess
+BMGC_DS00009,BMG_DS000009,,Acanthamoeba Keratitis,Acanthamoeba Keratitis,,,,,,C0000880,D015823,,MONDO:0005629,Acanthamoeba keratitis,
+BMGC_DS00010,BMG_DS000010,,Acanthosis Nigricans,Acanthosis Nigricans,,,,DOID:3138,acanthosis nigricans,C0000889,D000052,,MONDO:0007035,acanthosis nigricans,
+BMGC_DS00011,BMG_DS000011,,,,,,,,,C0001075,,,MONDO:0043465,achlorhydria,
+BMGC_DS00012,BMG_DS000012,,,,,,,,,C0001079,,,MONDO:0019648,achondrogenesis,
+BMGC_DS00013,BMG_DS000013,,,,,,,DOID:4480,achondroplasia,C0001080,,100800,MONDO:0007037,Achondroplasia,
+BMGC_DS00014,BMG_DS000014,,,,,,,,,C0001122,,,MONDO:0006022,acidosis disorder,
+BMGC_DS00015,BMG_DS000015,,"Acidosis, Lactic","Acidosis, Lactic",,,,DOID:3650,lactic acidosis,C0001125,D000140,,MONDO:0006040;MONDO:0024306,acquired lactic acidosis | lactic acidosis,
+BMGC_DS00016,BMG_DS000016,1776003,Renal tubular acidosis,,,,,DOID:14219,renal tubular acidosis,C0001126,,MTHU006717,MONDO:0001909,renal tubular acidosis,Renal tubular acidosis | Renal tubular acidosis (disorder) | RTA - Renal tubular acidosis | Renotubular acidaemia | Renotubular acidemia
+BMGC_DS00017,BMG_DS000017,,"Acidosis, Respiratory","Acidosis, Respiratory",,,,,,C0001127,D000142,,,,
+BMGC_DS00018,BMG_DS000018,,Acinetobacter Infections,Acinetobacter Infections,,,,,,C0001139,D000151,,MONDO:0006635,Acinetobacter infectious disease,
+BMGC_DS00019,BMG_DS000020,,Acne Vulgaris,Acne Vulgaris,,,,,,C0001144,D000152,,,,
+BMGC_DS00020,BMG_DS000022,,Vestibulocochlear Nerve Diseases,Vestibulocochlear Nerve Diseases,,,,DOID:12657,vestibulocochlear nerve disease,C0001163,D000160,,MONDO:0001563,vestibulocochlear nerve disorder,
+BMGC_DS00021,BMG_DS000024,,Acquired Immunodeficiency Syndrome,Acquired Immunodeficiency Syndrome,,,,DOID:635,acquired immunodeficiency syndrome,C0001175,D000163,,MONDO:0012268,AIDS,
+BMGC_DS00022,BMG_DS000025,,,,,,,,,C0001193,,101200,MONDO:0007041,Apert syndrome,
+BMGC_DS00023,BMG_DS000026,8197001,Acrodermatitis,Acrodermatitis,,,,DOID:2722,acrodermatitis,C0001197,D000169,,MONDO:0006523,acrodermatitis,Acrodermatitis | Acrodermatitis (disorder)
+BMGC_DS00024,BMG_DS000028,74107003;267480001;154698000,Acromegaly,Acromegaly,,,,DOID:2449,acromegaly,C0001206,D000172,MTHU016146,MONDO:0019933,acromegaly,"Acromegaly | Growth hormone hypersecretion syndrome | STH hypersecretion syndrome | Marie disease | Anterior pituitary adenoma syndrome | Acromegalia | Acromegaly (disorder) | (Acromegaly &/or gigantism) or (pituitary hyperfunction, ant.) | Gigantism and acromegaly | Anterior pituitary hyperfunction | Acromegaly and gigantism | Acromegaly | Gigantism | Pituitary hyperfunction (ant.) | (Acromegaly &/or gigantism) or (pituitary hyperfunction, ant.) (disorder) | Gigantism and acromegaly | Acromegaly and gigantism | Acromegaly | Gigantism | Pituitary hyperfunction (ant.) | Anterior pituitary hyperfunction | (Acromegaly &/or gigantism) or (pituitary hyperfunction, ant.) | (Acromegaly &/or gigantism) or (pituitary hyperfunction, ant.) (disorder)"
+BMGC_DS00025,BMG_DS000029,86073008,Hypersomatotropic gigantism,,,,,,,C0001207,,,,,Hypersomatotropic gigantism | Acromegalic gigantism | Pituitary gigantism | Launois syndrome | Hypersomatotropic gigantism (disorder)
+BMGC_DS00026,BMG_DS000030,,"ACTH Syndrome, Ectopic","ACTH Syndrome, Ectopic",,,,,,C0001231,D000182,,MONDO:0043472,ectopic ACTH secretion syndrome,
+BMGC_DS00027,BMG_DS000034,11817007;50508009;154314007;266185008,Actinomycosis,Actinomycosis,,,A42,DOID:8478,actinomycosis,C0001261,D000196,,MONDO:0005631,actinomycosis,Actinomycotic infection | Actinomycosis | Actinomycotic infection (disorder) | Actinomycosis | Actinomycosis (disorder) | (Actinomycosis (& [infections]) or (erythrasma) | Actinomycosis | Erythrasma | Actinomycotic infections | (Actinomycosis (& [infections]) or (erythrasma) (disorder) | (Actinomycosis (& [infections]) or (erythrasma) | Erythrasma | Actinomycotic infections | Actinomycosis | (Actinomycosis (& [infections]) or (erythrasma) (disorder)
+BMGC_DS00028,BMG_DS000035,43894001,Abdominal actinomycosis,,1C10.1,Abdominal actinomycosis,A42.1,,,C0001263,,,,,Abdominal actinomycosis | Ray fungus disease of the intestines | Abdominal actinomycosis (disorder)
+BMGC_DS00029,BMG_DS000036,23014006,Cervicofacial actinomycosis,,1C10.2,Cervicofacial actinomycosis,A42.2,,,C0001264,,,MONDO:0005699,cervicofacial actinomycosis,Cervicofacial actinomycosis | Cervicofacial actinomycosis (disorder)
+BMGC_DS00030,BMG_DS000039,9953008,Acute alcoholic liver disease,,,,,DOID:12351,alcoholic hepatitis,C0001306,,,,,Acute alcoholic liver disease | Acute alcoholic hepatitis | Acute alcoholic liver disease (disorder)
+BMGC_DS00031,BMG_DS000040,197268000,Acute and subacute liver necrosis (disorder),,,,,DOID:2237,hepatitis,C0001308,,,,,Acute and subacute liver necrosis | Acute and subacute liver necrosis (disorder)
+BMGC_DS00032,BMG_DS000041,193863004;67678004,Acute atopic conjunctivitis,,9A60.0Z,"Papillary conjunctivitis, unspecified",H10.1,DOID:11203,Angelucci's syndrome,C0001309,,,MONDO:0001224,Angelucci syndrome,Acute atopic conjunctivitis | Acute atopic conjunctivitis (disorder) | Acute atopic conjunctivitis | Angelucci's syndrome | Critical allergic conjunctivitis syndrome | Acute atopic conjunctivitis (disorder) | Acute allergic conjunctivitis
+BMGC_DS00033,BMG_DS000043,,Acute Disease,Acute Disease,,,,,,C0001314,D000208,,MONDO:0020683,acute disease,
+BMGC_DS00034,BMG_DS000044,155506009;6655004,Acute laryngitis,,CA05.0,Acute laryngitis,J04.0,DOID:9396,acute laryngitis,C0001327,,,MONDO:0004777,acute laryngitis,Acute laryngitis | Acute laryngitis (disorder)
+BMGC_DS00035,BMG_DS000045,,Herpetic Acute Necrotizing Encephalitis,"Encephalitis, Herpes Simplex",,,,,,C0001338,D020803,,,,
+BMGC_DS00036,BMG_DS000046,,"Pancreatitis, Acute",Pancreatitis,,,,DOID:2913,acute pancreatitis,C0001339,D010195,,MONDO:0006515,acute pancreatitis,
+BMGC_DS00037,BMG_DS000047,21638000;196361004;155646007,Acute periodontitis,,,,,DOID:10423,acute pericementitis,C0001342,,,MONDO:0001028,acute pericementitis,Acute periodontitis | Acute pericementitis | Acute periodontitis (disorder) | Acute periodontitis | Acute periodontitis (disorder)
+BMGC_DS00038,BMG_DS000048,195654001;155502006;27321001;266379007;363746003,Acute pharyngitis,,,,J02,DOID:2275,pharyngitis,C0001344,,,MONDO:0020600,acute pharyngitis,Throat: [acute pharyngitis] or [sore NOS (& viral)] or [infection] | Throat infection - pharyngitis | Sore throat NOS | Viral sore throat NOS | Acute pharyngitis | Throat: [acute pharyngitis] or [sore NOS (& viral)] or [infection] (disorder) | Acute pharyngitis | Pharyngitis - acute | Throat infection NOS | Sore throat | Throat: [acute pharyngitis] or [infection NOS] or [sore] | Throat: [acute pharyngitis] or [infection NOS] or [sore] (disorder) | Acute pharyngitis | Acute pharyngitis (disorder) | Sore throat | Acute pharyngitis | Pharyngitis - acute | Throat infection NOS | Throat: [acute pharyngitis] or [infection NOS] or [sore] | Throat: [acute pharyngitis] or [infection NOS] or [sore] (disorder)
+BMGC_DS00039,BMG_DS000049,154665005;190293001,Acute thyroiditis,,5A03.0,Acute thyroiditis,E06.0,DOID:14353,acute thyroiditis,C0001360,,,MONDO:0001949,acute thyroiditis,Acute thyroiditis | Acute thyroiditis (disorder)
+BMGC_DS00040,BMG_DS000051,91489000,Acute vascular insufficiency of intestine (disorder),,,,,DOID:8590,acute vascular insufficiency of intestine,C0001363,,,MONDO:0004613,acute intestinal ischemia,Acute vascular insufficiency of intestine | Acute intestinal ischemic syndrome | Acute intestinal vascular insufficiency | Acute intestinal ischemia | Acute mesenteric ischemia | AMI - Acute mesenteric ischemia | Acute intestinal ischaemia | Acute mesenteric ischaemia | AMI - Acute mesenteric ischaemia | Acute intestinal ischaemic syndrome | Acute vascular insufficiency of intestine (disorder)
+BMGC_DS00041,BMG_DS000053,,Adams-Stokes Syndrome,Adams-Stokes Syndrome,,,,,,C0001396,D000219,,MONDO:0043475,Adams-Stokes syndrome,
+BMGC_DS00042,BMG_DS000054,,Addison Disease,Addison Disease,,,,DOID:13774,Addison's disease,C0001403,D000224,240200,MONDO:0015129,chronic primary adrenal insufficiency,
+BMGC_DS00043,BMG_DS000055,,,,,,,DOID:299,adenocarcinoma,C0001418,,,MONDO:0004970,adenocarcinoma,
+BMGC_DS00044,BMG_DS000056,,,,,,,DOID:3112,papillary adenocarcinoma,C0001420,,,MONDO:0002512,papillary adenocarcinoma,
+BMGC_DS00045,BMG_DS000057,,,,,,,DOID:2683,adenofibroma,C0001422,,,MONDO:0006071,adenofibroma,
+BMGC_DS00046,BMG_DS000060,,,,,,,DOID:657,adenoma,C0001430,,,MONDO:0004972,adenoma,
+BMGC_DS00047,BMG_DS000061,,,,,,,DOID:4542,basophil adenoma,C0001431,,,MONDO:0006673,pituitary gland basophil adenoma,
+BMGC_DS00048,BMG_DS000062,,,,,,,DOID:3828,chromophobe adenoma,C0001432,,,MONDO:0006701,chromophobe adenoma,
+BMGC_DS00049,BMG_DS000063,,,,,,,DOID:5392,acidophil adenoma,C0001433,,,MONDO:0006634,pituitary gland acidophil adenoma,
+BMGC_DS00050,BMG_DS000064,,,,,,,DOID:1974,adenosarcoma,C0001442,,,MONDO:0005636,adenosarcoma,
+BMGC_DS00051,BMG_DS000065,,,,,,,DOID:0050117,disease by infectious agent,C0001485,,,,,
+BMGC_DS00052,BMG_DS000068,,Adie Syndrome,Adie Syndrome,,,,DOID:11549,Adie syndrome,C0001519,D000270,103100,MONDO:0018690,Holmes-Adie syndrome,
+BMGC_DS00053,BMG_DS000069,,Adiposis Dolorosa,Adiposis Dolorosa,,,,DOID:3928,adiposis dolorosa,C0001529,D000274,103200,MONDO:0007070,adiposis dolorosa,
+BMGC_DS00054,BMG_DS000073,,Adrenal Cortex Diseases,Adrenal Cortex Diseases,,,,DOID:3952,adrenal cortex disease,C0001614,D000303,,MONDO:0002816,adrenal cortex disorder,
+BMGC_DS00055,BMG_DS000074,,,,,,,DOID:660,adrenal cortex cancer,C0001618,,,MONDO:0036591,adrenal cortex neoplasm,
+BMGC_DS00056,BMG_DS000075,,Adrenal Gland Diseases,Adrenal Gland Diseases,,,,DOID:9553,adrenal gland disease,C0001621,D000307,,,,
+BMGC_DS00057,BMG_DS000076,,Adrenal Gland Hyperfunction,Adrenocortical Hyperfunction,,,,DOID:3947,adrenal gland hyperfunction,C0001622,D000308,,MONDO:0006640,adrenal gland hyperfunction,
+BMGC_DS00058,BMG_DS000077,,,,,,,DOID:3953,adrenal gland cancer,C0001624,,,MONDO:0021227,adrenal gland neoplasm,
+BMGC_DS00059,BMG_DS000078,237751000;27037004,Congenital adrenal hyperplasia,,5A71.01,Congenital adrenal hyperplasia,E25.0,,,C0001627,,MTHU014663,MONDO:0018479,congenital adrenal hyperplasia,Congenital adrenal hyperplasia | CAH - Congenital adrenal hyperplasia | Congenital adrenal cortical hyperplasia | Congenital adrenal hyperplasia (disorder) | Congenital adrenogenital syndrome | Congenital adrenal cortical hyperplasia | Congenital adrenal cortical hyperplasia (disorder)
+BMGC_DS00060,BMG_DS000081,,Afferent Loop Syndrome,Afferent Loop Syndrome,,,,DOID:8438,afferent loop syndrome,C0001727,D000343,,MONDO:0006641,afferent loop syndrome,
+BMGC_DS00061,BMG_DS000082,278504009,Afibrinogenemia,Afibrinogenemia,,,,DOID:2236,congenital afibrinogenemia,C0001733,D000347,,,,Afibrinogenaemia | Afibrinogenemia | Afibrinogenemia (disorder)
+BMGC_DS00062,BMG_DS000085,119249001;190977001;81282009;267512002,Agammaglobulinemia,Agammaglobulinemia,,,,DOID:2583,agammaglobulinemia,C0001768,D000361,MTHU008328,MONDO:0015977,agammaglobulinemia,Agammaglobulinemia | Agammaglobulinaemia | Agammaglobulinemia (finding) | (Deficiencies of humoral immunity) or (agammaglobulinemia) | Deficiencies of humoral immunity | Agammaglobulinemia | Agammaglobulinaemia | (Deficiencies of humoral immunity) or (agammaglobulinaemia) | (Deficiencies of humoral immunity) or (agammaglobulinemia) (disorder) | Agammaglobulinemia (disorder) | Agammaglobulinemia | Agammaglobulinaemia | Agammaglobulinemia &/or hypo-gammaglobulinemia | A/Hypo-gammaglobulinaemia | Agammaglobulinaemia | Agammaglobulinaemia &/or hypo-gammaglobulinaemia | Agammaglobulinemia | Agammaglobulinaemia &/or hypo-gammaglobulinaemia (disorder)
+BMGC_DS00063,BMG_DS000086,,"Osteoporosis, Age-Related",Osteoporosis,,,,,,C0001787,D010024,,,,
+BMGC_DS00064,BMG_DS000087,,,,,,,DOID:4971,myelofibrosis,C0001815,,254450,MONDO:0009692,primary myelofibrosis,
+BMGC_DS00065,BMG_DS000088,,,,,,,DOID:4090,agnosia,C0001816,,,MONDO:0005638,agnosia,
+BMGC_DS00066,BMG_DS000089,,,,,,,DOID:593,agoraphobia,C0001818,,,MONDO:0003709,agoraphobia,
+BMGC_DS00067,BMG_DS000090,17182001;191336001;142919000;165508008;154830007,Agranulocytosis,Agranulocytosis,,,,DOID:12987,agranulocytosis,C0001824,D000380,MTHU074770,MONDO:0001609,agranulocytosis,Agranulocytosis | Agranulocytosis (disorder) | Schultz disease | (Agranulocytosis) or (Kostmann's syndrome) or (neutropenia) | Kostmann's syndrome | Neutropenia | Agranulocytosis | (Agranulocytosis) or (Kostmann's syndrome) or (neutropenia) (disorder) | Agranulocytosis | Agranulocytosis (disorder) | Agranulocytosis | Agranulocytosis (finding)
+BMGC_DS00068,BMG_DS000092,,Agricultural Workers' Diseases,Agricultural Workers' Diseases,,,,,,C0001828,D000382,,,,
+BMGC_DS00069,BMG_DS000093,,AIDS Dementia Complex,AIDS Dementia Complex,,,,,,C0001849,D015526,,MONDO:0020689,AIDS dementia complex,
+BMGC_DS00070,BMG_DS000095,38528001;51404004,Ainhum,Ainhum,EE7Y,Other specified disorders of cutaneous connective tissue,L94.6,DOID:11329,ainhum,C0001860,D000387,103400,MONDO:0007074,ainhum,Ainhum | Dactylolysis spontanea | Ainhum (disorder) | Ainhum - dactylolysis spontanea | Fibrous bands | Fibrous bands (morphologic abnormality)
+BMGC_DS00071,BMG_DS000096,,Airsickness,Motion Sickness,NF08.3,Motion sickness,T75.3,,,C0001882,D009041,,,,
+BMGC_DS00072,BMG_DS000097,,Airway Obstruction,Airway Obstruction,,,,,,C0001883,D000402,,MONDO:0002267,obstructive lung disease,
+BMGC_DS00073,BMG_DS000098,,Akinetic Mutism,Akinetic Mutism,,,,DOID:4267,akinetic mutism,C0001889,D000405,,MONDO:0005640,akinetic mutism,
+BMGC_DS00074,BMG_DS000099,,Akinetic Petit Mal,"Epilepsy, Absence",,,,DOID:0070309,absence epilepsy,C0001890,D004832,,,,
+BMGC_DS00075,BMG_DS000100,,Variola Minor,Smallpox,,,,DOID:9153,variola minor,C0001906,D012899,,MONDO:0004720,variola minor infection,
+BMGC_DS00076,BMG_DS000101,154738008;190695000;15890002;267498002;190688009,Albinism,Albinism,5C50.Z,"Inborn errors of amino acid or other organic acid metabolism, unspecified",E70.3,DOID:0060831;DOID:0090100;DOID:0110949,Griscelli syndrome | Waardenburg syndrome type 3 | ocular albinism with sensorineural deafness,C0001916,D000417,MTHU037234,MONDO:0043209,albinism,Albinism | Cystinuria | Glucose-6-phosphate dehydrogenase deficiency | Glycogen storage disease | Glucose-6-phosph.dehydr.defic. | Von Gierke's disease | von Gierke disease | Other amino-acid/carbohydrate | (Other amino acid/carbohydrate) or (albinism) or (cystinuria) or (glucose-6-phosphate dehydrogenase deficiency) or (galactosemia) or (glycogen storage disease) or (Von Gierke's disease) | (Other amino acid/carbohydrate) or (albinism) or (cystinuria) or (glucose-6-phosphate dehydrogenase deficiency) or (galactosaemia) or (glycogen storage disease) or (Von Gierke's disease) | Galactosaemia | Galactosemia | (Other amino acid/carbohydrate) or (albinism) or (cystinuria) or (glucose-6-phosphate dehydrogenase deficiency) or (galactosaemia) or (glycogen storage disease) or (Von Gierke's disease) (disorder) | Albinism (& [Klein-Waardenberg's syndrome]) | Klein-Waardenberg's syndrome | Albino | Albinism | Albinismus | Albinism (& [Klein-Waardenberg's syndrome]) (disorder) | Albinism | Albinismus | Albinism (disorder) | Cystinuria | Glucose-6-phosphate dehydrogenase deficiency | Albinism | Other amino-acid/carbohydrate | Glycogen storage disease | von Gierke disease | Von Gierke's disease | Glucose-6-phosph.dehydr.defic. | Galactosaemia | Galactosemia | (Other amino acid/carbohydrate) or (albinism) or (cystinuria) or (glucose-6-phosphate dehydrogenase deficiency) or (galactosaemia) or (glycogen storage disease) or (Von Gierke's disease) | (Other amino acid/carbohydrate) or (albinism) or (cystinuria) or (glucose-6-phosphate dehydrogenase deficiency) or (galactosemia) or (glycogen storage disease) or (Von Gierke's disease) | (Other amino acid/carbohydrate) or (albinism) or (cystinuria) or (glucose-6-phosphate dehydrogenase deficiency) or (galactosaemia) or (glycogen storage disease) or (Von Gierke's disease) (disorder) | Disorder of amino acid metabolism: [other aromatic] or [albinism] | Other disturbances of aromatic amino-acid metabolism | Albinism | Disorder of amino acid metabolism: [other aromatic] or [albinism] (disorder)
+BMGC_DS00077,BMG_DS000103,,Alcohol Withdrawal Delirium,Alcohol Withdrawal Delirium,,,,,,C0001957,D000430,,MONDO:0006642,alcohol withdrawal delirium,
+BMGC_DS00078,BMG_DS000104,,,,,,,,,C0001973,,103780,MONDO:0007079,alcohol dependence,
+BMGC_DS00079,BMG_DS000105,,Aleutian Mink Disease,Aleutian Mink Disease,,,,DOID:2934,aleutian mink disease,C0002016,D000453,,MONDO:0005641;MONDO:1010029,"aleutian mink disease | aleutian mink disease, human",
+BMGC_DS00080,BMG_DS000106,,,,,,,DOID:13417,alexia,C0002018,,,MONDO:0001712,alexia,
+BMGC_DS00081,BMG_DS000107,,,,,,,,,C0002020,,,MONDO:0000661,alexithymia,
+BMGC_DS00082,BMG_DS000108,154758009;21420006,Alkalosis,Alkalosis,5C74,Alkalosis,E87.3,,,C0002063,D000471,MTHU054076,,,Alkalosis | Alkalosis (disorder)
+BMGC_DS00083,BMG_DS000109,24250001;190689001;360378009;360381004,Alkaptonuria,Alkaptonuria,,,E70.29,DOID:9270,alkaptonuria,C0002066,D000474,203500,MONDO:0008753,alkaptonuria,"Alkaptonuria | Alkaptonuria (disorder) | Alkaptonuria | Homogentisic acid defect | Homogentisic acid defect (& alkaptonuria) | Homogentisic acid defect (& alkaptonuria) (disorder) | Homogentisicaciduria | Deficiency of homogentisate 1,2-dioxygenase | Deficiency of homogentisate oxygenase | Homogentisic acid oxidase deficiency | Deficiency of homogentisicase | Homogentisate 1,2-dioxygenase deficiency | Homogentisate 1,2-dioxygenase deficiency (disorder) | Hereditary ochronosis | Alkaptonuria | HGD-gene related homogentisate 1,2-dioxygenase deficiency | Alkaptonuria | Alkaptonuria (finding)"
+BMGC_DS00084,BMG_DS000111,38103000,Atopic rhinitis,,,,,DOID:4481,allergic rhinitis,C0002103,,,,,Atopic rhinitis | Atopic rhinitis (disorder)
+BMGC_DS00085,BMG_DS000114,56317004;270504008;156408004;201129005,Alopecia,Alopecia,,,,DOID:987,alopecia,C0002170,D000505,MTHU036686,MONDO:0004907,alopecia,Alopecia | Baldness | Bald | Hair loss disorder | Alopecia (disorder) | Alopecia | Hair loss disorder | Baldness | Bald | Alopecia (disorder) | Alopecia | Alopecia (disorder) | (Alopecia) or (thinning of hair) | Alopecia | Thinning of hair | (Alopecia) or (thinning of hair) (disorder)
+BMGC_DS00086,BMG_DS000115,,Alopecia Areata,Alopecia Areata,,,,DOID:986,alopecia areata,C0002171,D000506,,MONDO:0005340,alopecia areata,
+BMGC_DS00087,BMG_DS000116,,"Mucinosis, Follicular","Mucinosis, Follicular",,,,DOID:9905,follicular mucinosis,C0002173,D000507,,MONDO:0006551,alopecia mucinosa,
+BMGC_DS00088,BMG_DS000123,,alpha-Thalassemia,alpha-Thalassemia,,,,DOID:1099,alpha thalassemia,C0002312,D017085,604131,MONDO:0011399,alpha thalassemia spectrum,
+BMGC_DS00089,BMG_DS000124,,Altitude Sickness,Altitude Sickness,,,,,,C0002351,D000532,,MONDO:0006625,altitude sickness,
+BMGC_DS00090,BMG_DS000125,,Alveolar Bone Loss,Alveolar Bone Loss,,,,,,C0002382,D016301,,,,
+BMGC_DS00091,BMG_DS000126,37471005;266399001;155581001,Extrinsic allergic alveolitis,,,,,DOID:841,extrinsic allergic alveolitis,C0002390,,,MONDO:0017853,hypersensitivity pneumonitis,"Extrinsic allergic alveolitis | Extrinsic allergic bronchiolo-alveolitis | Allergic alveolitis | Allergic pneumonitis | Allergic interstitial pneumonitis | Hypersensitivity pneumonitis | EAA - Extrinsic allergic alveolitis | Bagpipe lung | Hypersensitivity pneumonitis (disorder) | (Extrinsic allergic alveolitis) or (farmers' lung) or (pneumonitis, allergic NOS) | Extrinsic allergic alveolitis | Farmers' lung | Alveolitis - allergic | Pneumonitis, allergic NOS | Farmers lung | Allergic alveolitis | Extrinsic allergic alveolitis | Farmers lung | Alveolitis - allergic | Allergic alveolitis | Pneumonitis, allergic NOS | Farmers' lung | (Extrinsic allergic alveolitis) or (farmers' lung) or (pneumonitis, allergic NOS)"
+BMGC_DS00092,BMG_DS000127,,Alzheimer's Disease,Alzheimer Disease,,,,DOID:10652,Alzheimer's disease,C0002395,D000544,,MONDO:0004975,Alzheimer disease,
+BMGC_DS00093,BMG_DS000128,155145007;267726008;111517004;387742006,Amblyopia,Amblyopia,,,,DOID:10376,amblyopia,C0002418,D000550,MTHU002370,MONDO:0001020,amblyopia,(Visual disturbances NOS) or (amblyopia) or (blurred vision) | Visual disturbances NOS | Amblyopia | Blurred vision | (Visual disturbances NOS) or (amblyopia) or (blurred vision) (disorder) | Amblyopia | Congenital amblyopia | Amblyopic | Functional amblyopia | Amblyopia (disorder) | Amblyopia (disorder) | Amblyopia | Amblyopic
+BMGC_DS00094,BMG_DS000129,30483005,Tobacco amblyopia,,,,,,,C0002419,,,,,Tobacco amblyopia | Tobacco amblyopia (disorder)
+BMGC_DS00095,BMG_DS000130,111909004;111910009;388759003;387754006;154274000,Amebiasis,Amebiasis,,,A06,DOID:9181,amebiasis,C0002438,D000562,,MONDO:0005644,amebiasis,Amebiasis | Amebic dysentery | Amoebic dysentery | Amoebiasis | Amebiasis (disorder) | Amebic infection | Amoebic infection | Amebic infection (disorder) | Amoebiasis | Amebiasis | Infection caused by Entamoeba histolytica | Infection caused by Entamoeba histolytica (disorder) | Entamoeba histolytica infection | Amebic dysentery (disorder) | Amoebic dysentery | Amebic dysentery | Amoebiasis | Amebiasis | Amoebiasis (disorder)
+BMGC_DS00096,BMG_DS000134,,,,,,,,,C0002448,,,MONDO:0017795,ameloblastoma,
+BMGC_DS00097,BMG_DS000135,,,,,,,DOID:2187,amelogenesis imperfecta,C0002452,,,MONDO:0019507,amelogenesis imperfecta,
+BMGC_DS00098,BMG_DS000136,,,,,,,DOID:13938,amenorrhea,C0002453,,,MONDO:0001836,amenorrhea,
+BMGC_DS00099,BMG_DS000137,,"Amino Acid Metabolism, Inborn Errors","Amino Acid Metabolism, Inborn Errors",,,,DOID:9252,amino acid metabolic disorder,C0002514,D000592,,,,
+BMGC_DS00100,BMG_DS000138,,Renal Aminoacidurias,Renal Aminoacidurias,,,,,,C0002534,D000608,,MONDO:0006944,renal aminoaciduria,
+BMGC_DS00101,BMG_DS000139,,,,,,,DOID:10914,amnestic disorder,C0002622,,,,,
+BMGC_DS00102,BMG_DS000140,,,,,,,DOID:4543,retrograde amnesia,C0002624,,,MONDO:0003040,retrograde amnesia,
+BMGC_DS00103,BMG_DS000141,,,,,,,DOID:10914,amnestic disorder,C0002625,,,MONDO:0001152,amnestic disorder,
+BMGC_DS00104,BMG_DS000142,10573002,Infection of amniotic cavity,,,,,,,C0002631,,,MONDO:0020710,amnionitis,Infection of amniotic cavity | Amnionitis | Infection of amniotic cavity (disorder) | Amniotic cavity infection
+BMGC_DS00105,BMG_DS000145,17602002;154769007,Amyloidosis,Amyloidosis,,,E85,DOID:9120,amyloidosis,C0002726,D000686,MTHU076637,MONDO:0019065,amyloidosis,Amyloidosis | Amyloidosis (disorder)
+BMGC_DS00106,BMG_DS000146,,Oppenheim's Disease,Neuromuscular Diseases,,,,,,C0002735,D009468,205000,MONDO:0056822,amyotonia congenita,
+BMGC_DS00107,BMG_DS000147,,Amyotrophic Lateral Sclerosis,Amyotrophic Lateral Sclerosis,,,,DOID:332,amyotrophic lateral sclerosis,C0002736,D000690,,MONDO:0004976,amyotrophic lateral sclerosis,
+BMGC_DS00108,BMG_DS000148,,,,,,,DOID:4550,anal gland neoplasm,C0002757,,,MONDO:0003045,anal gland neoplasm,
+BMGC_DS00109,BMG_DS000149,,Congenital Pain Insensitivity,"Pain Insensitivity, Congenital",,,,DOID:0070145,hereditary sensory and autonomic neuropathy type 5,C0002768,D000699,,,,
+BMGC_DS00110,BMG_DS000152,85807000;63479002,Ancylostomiasis,Ancylostomiasis,1F68,Hookworm diseases,B76.0,DOID:12841,ancylostomiasis,C0002831,D000724,,MONDO:0005645,ancylostomiasis,Infection by Uncinaria | Uncinariasis | Uncinariosis | Ancylostomiasis | Ancylostomiasis due to Ancylostoma duodenale | Ancylostomosis | Hookworm infection | Infection by Uncinaria (disorder) | Ancylostomiasis | Ancylostomiasis (disorder)
+BMGC_DS00111,BMG_DS000153,271737000;64593003;154786001,Anemia,Anemia,,,,DOID:2355,anemia,C0002871,D000740,MTHU002606,MONDO:0002280,anemia,Anemia | Anaemia | Absolute anemia | Absolute anaemia | Anemia (disorder) | Anemia | Anaemia | Anemia (disorder) | Anemia | Anaemia | Anaemia (disorder)
+BMGC_DS00112,BMG_DS000155,,Aplastic Anemia,"Anemia, Aplastic",,,,DOID:12449,aplastic anemia,C0002874,D000741,,MONDO:0015909,aplastic anemia,
+BMGC_DS00113,BMG_DS000156,26682008,Cooley's anemia,,3A50.2,Beta thalassaemia,D56.1,,,C0002875,,,MONDO:0016486,beta-thalassemia major,Homozygous beta thalassemia | Cooley's anemia | Mediterranean anemia | Beta thalassaemia major | Cooley's anaemia | Homozygous beta thalassaemia | Homozygous beta thalassemia (disorder)
+BMGC_DS00114,BMG_DS000157,191272005;52951008,Congenital dyserythropoietic anemia,,3A73,Congenital dyserythropoietic anaemia,D64.4,DOID:1338,congenital dyserythropoietic anemia,C0002876,,MTHU074604,MONDO:0019403,congenital dyserythropoietic anemia,Congenital anemia: [dyshematopoietic] or [dyserythropoietic (& NEC)] | Congenital dyserythropoiesis NEC | Congenital dyserythropoietic anemia | Congenital dyshematopoietic anemia | Congenital dyserythropoietic anaemia | Congenital dyshaematopoietic anaemia | Congenital anaemia: [dyshaematopoietic] or [dyserythropoietic (& NEC)] | Congenital anaemia: [dyshaematopoietic] or [dyserythropoietic (& NEC)] (disorder) | Congenital dyserythropoietic anemia | Congenital dyserythropoietic anaemia | Congenital dyserythropoietic anemia (disorder) | CDA - congenital dyserythropoietic anaemia | CDA - congenital dyserythropoietic anemia
+BMGC_DS00115,BMG_DS000158,,"Anemia, Hemolytic","Anemia, Hemolytic",,,,DOID:583,hemolytic anemia,C0002878,D000743,,MONDO:0003664,hemolytic anemia,
+BMGC_DS00116,BMG_DS000159,,"Anemia, Hemolytic, Acquired","Anemia, Hemolytic",,,,,,C0002879,D000743,,,,
+BMGC_DS00117,BMG_DS000160,25121006;154803002;413603009,Autoimmune hemolytic anemia,,,,,DOID:718,autoimmune hemolytic anemia,C0002880,,MTHU002424;205700,MONDO:0020108,autoimmune hemolytic anemia,Autoimmune hemolytic anemia | Neonatal isoerythrolysis | Hemolytic anemia due to antibody | Autoimmune haemolytic anaemia | AIHA - Autoimmune haemolytic anaemia | AIHA - Autoimmune hemolytic anemia | Haemolytic anaemia due to antibody | Autoimmune hemolytic anemia (disorder) | Autoimmune hemolytic anemia | Autoimmune haemolytic anaemia | Autoimmune haemolytic anaemia (disorder) | Autoimmune hemolytic anemia (disorder) | Autoimmune hemolytic anemia | Autoimmune haemolytic anaemia
+BMGC_DS00118,BMG_DS000161,,"Anemia, Hemolytic, Congenital","Anemia, Hemolytic, Congenital",,,,DOID:589,congenital hemolytic anemia,C0002881,D000745,,MONDO:0003689,familial hemolytic anemia,
+BMGC_DS00119,BMG_DS000162,,"Anemia, Hemolytic, Congenital Nonspherocytic","Anemia, Hemolytic, Congenital Nonspherocytic",,,,DOID:2861,congenital nonspherocytic hemolytic anemia,C0002882,D000746,,MONDO:0006506,congenital nonspherocytic hemolytic anemia,
+BMGC_DS00120,BMG_DS000163,,"Anemia, Hemolytic, Idiopathic Acquired","Anemia, Hemolytic, Autoimmune",,,,,,C0002883,D000744,,,,
+BMGC_DS00121,BMG_DS000164,44452003,Hypochromic anemia,,,,,DOID:11759,hypochromic anemia,C0002884,,MTHU006440,MONDO:0001357,hypochromic anemia,Normocytic hypochromic anemia | Hypochromic anemia | Hypochromic anaemia | Normocytic hypochromic anaemia | Normocytic hypochromic anemia (disorder)
+BMGC_DS00122,BMG_DS000165,,"Anemia, Macrocytic","Anemia, Macrocytic",,,,DOID:2361,macrocytic anemia,C0002886,D000748,,MONDO:0002281,macrocytic anemia,
+BMGC_DS00123,BMG_DS000166,,"Anemia, Megaloblastic","Anemia, Megaloblastic",,,,DOID:13382,megaloblastic anemia,C0002888,D000749,,MONDO:0001700,megaloblastic anemia,
+BMGC_DS00124,BMG_DS000167,,"Anemia, Microangiopathic","Anemia, Hemolytic",,,,,,C0002889,D000743,,,,
+BMGC_DS00125,BMG_DS000168,,Leukoerythroblastic Anemia,"Anemia, Myelophthisic",,,,DOID:2354,myelophthisic anemia,C0002890,D000750,,MONDO:0005868,myelophthisic anemia,
+BMGC_DS00126,BMG_DS000169,,"Anemia, Neonatal","Anemia, Neonatal",,,,DOID:11244,neonatal anemia,C0002891,D000751,,MONDO:0001240,neonatal anemia,
+BMGC_DS00127,BMG_DS000170,,"Anemia, Pernicious","Anemia, Pernicious",,,,DOID:13381,pernicious anemia,C0002892,D000752,170900,MONDO:0008228,pernicious anemia,
+BMGC_DS00128,BMG_DS000172,,"Anemia, Sickle Cell","Anemia, Sickle Cell",,,,DOID:10923,sickle cell anemia,C0002895,D000755,603903,MONDO:0011382,sickle cell anemia,
+BMGC_DS00129,BMG_DS000173,41841004;154810008,Sideroblastic anemia,,,,,DOID:8955,sideroblastic anemia,C0002896,,MTHU037698,MONDO:0015194,sideroblastic anemia,Sideroblastic anemia | Primary sideroblastic anemia | Refractory sideroblastic anemia | Sideroachrestic anemia | Primary sideroblastic anaemia | Sideroachrestic anaemia | Refractory sideroblastic anaemia | Sideroblastic anaemia | Sideroblastic anemia (disorder) | Sideroblastic anaemia | Sideroblastic anemia | Sideroblastic anaemia (disorder)
+BMGC_DS00130,BMG_DS000174,,"Anemia, Splenic",Hypersplenism,,,,,,C0002897,D006971,,,,
+BMGC_DS00131,BMG_DS000175,,,,,,,,,C0002902,,,MONDO:0000819,anencephaly,
+BMGC_DS00132,BMG_DS000176,,,,,,,,,C0002938,,,MONDO:0700064,aneuploidy,
+BMGC_DS00133,BMG_DS000177,,,,,,,DOID:178,vascular disease,C0002940,,,,,
+BMGC_DS00134,BMG_DS000178,,Arterial Dissection,"Dissection, Blood Vessel",,,,,,C0002949,D000094665,,,,
+BMGC_DS00135,BMG_DS000181,,"Angina Pectoris, Variant","Angina Pectoris, Variant",,,,DOID:0111151,Prinzmetal angina,C0002963,D000788,,MONDO:0006021,Prinzmetal angina,
+BMGC_DS00136,BMG_DS000182,,"Angina, Unstable","Angina, Unstable",,,,DOID:8805,intermediate coronary syndrome,C0002965,D000789,,MONDO:0006805,intermediate coronary syndrome,
+BMGC_DS00137,BMG_DS000183,,Angioid Streaks,Angioid Streaks,,,,DOID:13401,angioid streaks,C0002982,D000793,607140,MONDO:0011782,angioid streaks,
+BMGC_DS00138,BMG_DS000184,86103006,Angioid streaks of choroid,,,,,DOID:979,angioid streaks of choroid,C0002983,,,MONDO:0004882,angioid streaks of choroid,Angioid streaks of choroid | Angioid streaks of choroid (disorder)
+BMGC_DS00139,BMG_DS000185,,,,,,,DOID:479,angiokeratoma,C0002985,,,MONDO:0003143,angiokeratoma,
+BMGC_DS00140,BMG_DS000186,,Fabry Disease,Fabry Disease,,,,DOID:14499,Fabry disease,C0002986,D000795,301500,MONDO:0010526,Fabry disease,
+BMGC_DS00141,BMG_DS000187,,,,,,,DOID:14308,skin epithelioid hemangioma,C0002989,,,MONDO:0001939,skin epithelioid hemangioma,
+BMGC_DS00142,BMG_DS000188,,,,,,,DOID:4418,cutaneous fibrous histiocytoma,C0002991,,,MONDO:0006717,cutaneous fibrous histiocytoma,
+BMGC_DS00143,BMG_DS000190,,,,,,,DOID:1558,angioedema,C0002994,,,MONDO:0010481,angioedema,
+BMGC_DS00144,BMG_DS000191,39659002;156414006;201189007,Anhidrosis,Hypohidrosis,EE01.Z,"Hypohidrosis, unspecified",L74.4,DOID:11156,anhidrosis,C0003028,D007007,MTHU001816,MONDO:0006560;MONDO:0006527,obsolete hypohidrosis | anhidrosis,Anhidrosis | Anhidrosis (disorder) | (Anhidrosis) or (hypohidrosis) or (oligohidrosis) | Oligohidrosis | Hypohidrosis | Anhidrosis | (Anhidrosis) or (hypohidrosis) or (oligohidrosis) (disorder)
+BMGC_DS00145,BMG_DS000193,,,,,,,DOID:12271,aniridia,C0003076,,,MONDO:0019172,aniridia,
+BMGC_DS00146,BMG_DS000196,3289004,Anisometropia,Anisometropia,,,H52.31,DOID:12273,anisometropia,C0003081,D015858,MTHU042450,MONDO:0001478,anisometropia,Anisometropia | Anisometropia (disorder)
+BMGC_DS00147,BMG_DS000197,,,,,,,DOID:417,autoimmune disease,C0003089,,,,,
+BMGC_DS00148,BMG_DS000198,,,,,,,DOID:227,ankylosis,C0003090,,,MONDO:0002257,ankylosis,
+BMGC_DS00149,BMG_DS000201,,,,,,,DOID:4541,nominal aphasia,C0003113,,,MONDO:0003039,nominal aphasia,
+BMGC_DS00150,BMG_DS000202,,Anorexia,Anorexia,MG43.7,Anorexia,R63.0,,,C0003123,D000855,MTHU006757,,,
+BMGC_DS00151,BMG_DS000203,,,,,,,DOID:8689,anorexia nervosa,C0003125,,,MONDO:0005351,anorexia nervosa,
+BMGC_DS00152,BMG_DS000204,,,,,,,,,C0003126,,,MONDO:0010528,anosmia,
+BMGC_DS00153,BMG_DS000205,34571000,Anovulation,Anovulation,,,,DOID:3781,anovulation,C0003128,D000858,,MONDO:0002775,anovulation,Anovulation | Anovulation (finding) | Ovulation absent
+BMGC_DS00154,BMG_DS000206,,Anterior Compartment Syndrome,Anterior Compartment Syndrome,,,,DOID:3933,anterior compartment syndrome,C0003152,D000868,,MONDO:0006648,anterior compartment of tibia syndrome,
+BMGC_DS00155,BMG_DS000207,33548005,Anthracosilicosis,Anthracosilicosis,,,J60,DOID:10324,anthracosilicosis,C0003164,D000874,,MONDO:0006653,anthracosilicosis,Anthracosilicosis | Anthracosilicosis (disorder)
+BMGC_DS00156,BMG_DS000208,29422001,Anthracosis,Anthracosis,,,J60,DOID:10327,anthracosis,C0003165,D055008,,MONDO:0006654,anthracosis,Coal workers' pneumoconiosis | Coal pneumoconiosis | Colliers' lung | Colliers' anthracosis | Miners' lung | Melanedema | Anthracosis | Black lung disease | Coal workers' lung | Miners' asthma | Lung melanosis | Pneumomelanosis | Coal miners' lung | Coal miners' pneumoconiosis | Melanoedema | Coal workers' pneumoconiosis (disorder)
+BMGC_DS00157,BMG_DS000209,,,,,,,DOID:7427,anthrax disease,C0003175,,,MONDO:0005119,anthrax infection,
+BMGC_DS00158,BMG_DS000210,84980006,Cutaneous anthrax,,1B97,Anthrax,A22.0,DOID:7426,cutaneous anthrax,C0003177,C531621,,MONDO:0004215,cutaneous anthrax,Cutaneous anthrax | Malignant pustule | Cutaneous anthrax (disorder)
+BMGC_DS00159,BMG_DS000211,,Antibody Deficiency Syndrome,Immunologic Deficiency Syndromes,,,,,,C0003257,D007153,,,,
+BMGC_DS00160,BMG_DS000212,,,,,,,DOID:10939,antisocial personality disorder,C0003431,,,MONDO:0001164,antisocial personality disorder,
+BMGC_DS00161,BMG_DS000213,2472002;139460001,Anuria,Anuria,,,,DOID:2983,anuria,C0003460,D001002,MTHU012488,MONDO:0002476,anuria,Anuria | Anuria (finding) | Passes no urine | Anuria | Anuria (finding)
+BMGC_DS00162,BMG_DS000214,,Anus Diseases,Anus Diseases,,,,DOID:3128,anus disease,C0003462,D001004,,MONDO:0002519,anus disorder,
+BMGC_DS00163,BMG_DS000215,,,,,,,DOID:4551,anus benign neoplasm,C0003463,,,MONDO:0003046,anus neoplasm,
+BMGC_DS00164,BMG_DS000216,,,,,,,DOID:10488,imperforate anus,C0003466,,207500;301800,MONDO:0001046,imperforate anus,
+BMGC_DS00165,BMG_DS000217,,,,,,,,,C0003467,,607834,MONDO:0011918,anxiety,
+BMGC_DS00166,BMG_DS000218,,,,,,,DOID:2030,anxiety disorder,C0003469,,,MONDO:0005618,anxiety disorder,
+BMGC_DS00167,BMG_DS000219,,,,,,,,,C0003477,,,MONDO:0001098,separation anxiety disorder,
+BMGC_DS00168,BMG_DS000220,,Aortic Aneurysm,Aortic Aneurysm,,,,DOID:3627,aortic aneurysm,C0003486,D001014,,MONDO:0005160,aortic aneurysm,
+BMGC_DS00169,BMG_DS000221,,Aortic Arch Syndromes,Aortic Arch Syndromes,,,,DOID:2508,Takayasu's arteritis,C0003490,D001015,,,,
+BMGC_DS00170,BMG_DS000222,,,,,,,,,C0003492,,120000,MONDO:0007345,aorta coarctation,
+BMGC_DS00171,BMG_DS000223,,Aortic Diseases,Aortic Diseases,,,,DOID:520,aortic disease,C0003493,D001018,,MONDO:0005561,aortic disorder,
+BMGC_DS00172,BMG_DS000224,,Aortic Rupture,Aortic Rupture,,,,,,C0003496,D001019,,,,
+BMGC_DS00173,BMG_DS000225,,Supravalvular aortic stenosis,,LA8A.3,Congenital supravalvar aortic stenosis,Q25.3,DOID:1929,supravalvular aortic stenosis,C0003499,,MTHU014953;185500,MONDO:0008504,supravalvular aortic stenosis,
+BMGC_DS00174,BMG_DS000227,,Aortic Valve Insufficiency,Aortic Valve Insufficiency,,,,DOID:57,aortic valve insufficiency,C0003504,D001022,,MONDO:0005648,aortic valve insufficiency,
+BMGC_DS00175,BMG_DS000228,,Aortic Valve Prolapse,Aortic Valve Prolapse,,,,DOID:5232,aortic valve prolapse,C0003505,D001023,,MONDO:0006655,aortic valve prolapse,
+BMGC_DS00176,BMG_DS000229,,,,,,,DOID:1712,aortic valve stenosis,C0003507,,,MONDO:0042981,aortic valve stenosis,
+BMGC_DS00177,BMG_DS000230,70933002;195368003,Aortitis,Aortitis,,,,DOID:519,aortitis,C0003509,D001025,MTHU021216,MONDO:0006656,aortitis,Aortitis | Aortitis (disorder) | (Arteritis unspecified) or (aortitis) | Arteritis unspecified | Aortitis | (Arteritis unspecified) or (aortitis) (disorder)
+BMGC_DS00178,BMG_DS000231,,Aortitis Syndrome,Takayasu Arteritis,,,,,,C0003510,D013625,,,,
+BMGC_DS00179,BMG_DS000234,,,,,,,,,C0003537,,,MONDO:0000598,aphasia,
+BMGC_DS00180,BMG_DS000235,,,,,,,DOID:11240,appendiceal neoplasm,C0003614,,,MONDO:0001236,appendiceal neoplasm,
+BMGC_DS00181,BMG_DS000236,74400008;155728006;155729003,Appendicitis,Appendicitis,,,,DOID:8337,appendicitis,C0003615,D001064,,MONDO:0005649,appendicitis,Appendicitis | Appendicitis (disorder)
+BMGC_DS00182,BMG_DS000237,,,,,,,DOID:0060135,apraxia,C0003635,,,MONDO:0000665,apraxia,
+BMGC_DS00183,BMG_DS000238,8217007;267681007;154986008,Arachnoiditis,Arachnoiditis,,,,DOID:12156,arachnoiditis,C0003708,D001100,,MONDO:0015304,arachnoiditis,Arachnoiditis | Arachnoiditis (disorder) | Other meningitis NOS &/or arachnoiditis | Arachnoiditis | Other meningitis NOS | Other meningitis NOS &/or arachnoiditis (disorder) | Other meningitis NOS &/or arachnoiditis | Other meningitis NOS | Arachnoiditis | Other meningitis NOS &/or arachnoiditis (disorder)
+BMGC_DS00184,BMG_DS000240,,Arbovirus Infections,Arbovirus Infections,,,,DOID:934,viral infectious disease,C0003723,D001102,,MONDO:0020731,arbovirus infection,
+BMGC_DS00185,BMG_DS000241,,Arcus Senilis,Arcus Senilis,,,,DOID:11342,arcus senilis,C0003742,D001112,107800,MONDO:0007150,arcus senilis,
+BMGC_DS00186,BMG_DS000242,,Arenaviridae Infections,Arenaviridae Infections,,,,,,C0003756,D001117,,MONDO:0005650,Arenaviridae infectious disease,
+BMGC_DS00187,BMG_DS000243,,,,,,,,,C0003803,,,MONDO:0000115,Chiari malformation,
+BMGC_DS00188,BMG_DS000245,,Cardiac Arrhythmia,"Arrhythmias, Cardiac",,,,,,C0003811,D001145,,MONDO:0007263,cardiac rhythm disease,
+BMGC_DS00189,BMG_DS000247,,Arterial Occlusive Diseases,Arterial Occlusive Diseases,,,,DOID:341,peripheral vascular disease,C0003838,D001157,,,,
+BMGC_DS00190,BMG_DS000249,195251000;28960008,Arteriosclerosis,Arteriosclerosis,,,,DOID:2349,arteriosclerosis,C0003850,D001161,MTHU037126,MONDO:0002277,arteriosclerosis disorder,Atherosclerotic cardiovascular disease | Arteriosclerosis | AS - Atherosclerosis | Atherosclerosis | Atherosclerosis (disorder) | Arteriosclerosis | Arteriosclerosis (morphologic abnormality)
+BMGC_DS00191,BMG_DS000250,,Arteriosclerosis Obliterans,Arteriosclerosis Obliterans,,,,DOID:5160,arteriosclerosis obliterans,C0003851,D001162,,MONDO:0006659,arteriosclerosis obliterans,
+BMGC_DS00192,BMG_DS000251,,,,,,,,,C0003860,,,MONDO:0043494,arteritis,
+BMGC_DS00193,BMG_DS000253,3723001;202059001;372091005,Arthritis,Arthritis,,,,DOID:848,arthritis,C0003864,D001168,MTHU001688,MONDO:0005578,arthritic joint disease,Arthritis | Arthritis (disorder) | Inflammatory arthritis | (Arthropathy NOS) or (arthritis) | Arthritis | Arthropathy NOS | (Arthropathy NOS) or (arthritis) (disorder) | Arthritis (finding) | Arthritis
+BMGC_DS00194,BMG_DS000254,,"Arthritis, Gouty","Arthritis, Gouty",,,,DOID:13189,gout,C0003868,D015210,,,,
+BMGC_DS00195,BMG_DS000255,,"Arthritis, Infectious","Arthritis, Infectious",,,,DOID:813,septic arthritis,C0003869,D001170,,MONDO:0042485,infective arthritis,
+BMGC_DS00196,BMG_DS000256,,"Arthritis, Psoriatic","Arthritis, Psoriatic",,,,DOID:9008,psoriatic arthritis,C0003872,D015535,,MONDO:0011849,psoriatic arthritis,
+BMGC_DS00197,BMG_DS000257,,Rheumatoid Arthritis,"Arthritis, Rheumatoid",,,,DOID:7148,rheumatoid arthritis,C0003873,D001172,180300,MONDO:0008383,rheumatoid arthritis,
+BMGC_DS00198,BMG_DS000259,,"Arthritis, Viral","Arthritis, Infectious",,,,,,C0003875,D001170,,,,
+BMGC_DS00199,BMG_DS000261,,,,,,,DOID:14286,neurogenic arthropathy,C0003892,,,MONDO:0001935,neurogenic arthropathy,
+BMGC_DS00200,BMG_DS000262,,Arthus Reaction,Arthus Reaction,,,,DOID:1556,arthus reaction,C0003907,D001183,,MONDO:0006660,arthus reaction,
+BMGC_DS00201,BMG_DS000263,,,,,,,DOID:4186,articulation disorder,C0003910,,,MONDO:0002903,articulation disorder,
+BMGC_DS00202,BMG_DS000264,22607003;155589004;266400008,Asbestosis,Asbestosis,,,J61,DOID:10320,asbestosis,C0003949,D001195,,MONDO:0016466,asbestosis,Asbestosis | Amianthosis | Asbestos pneumoconiosis | Asbestosis (disorder) | Pulmonary asbestosis | (Asbestosis) or (byssinosis) or (pleural plaque disease) | Pleural plaque disease | Asbestosis | Byssinosis | (Asbestosis) or (byssinosis) or (pleural plaque disease) (disorder) | Byssinosis | Asbestosis | Pleural plaque disease | (Asbestosis) or (byssinosis) or (pleural plaque disease) | (Asbestosis) or (byssinosis) or (pleural plaque disease) (disorder)
+BMGC_DS00203,BMG_DS000265,2435008,Ascariasis,Ascariasis,,,B77,DOID:456,ascariasis,C0003950,D001196,,MONDO:0005654,ascariasis,Ascariasis | Ascariosis | Ascaridiasis | Ascariasis - roundworms | Ascariasis (disorder)
+BMGC_DS00204,BMG_DS000266,2435008,Ascaridiasis,Ascaridiasis,,,,DOID:3108,ascaridiasis,C0003952,D001198,,MONDO:0005655,ascaridiasis,Ascariasis | Ascariosis | Ascaridiasis | Ascariasis - roundworms | Ascariasis (disorder)
+BMGC_DS00205,BMG_DS000267,13124004;389026000,Ascites,Ascites,,,R18,,,C0003962,D001201,MTHU037219,,,Ascites | Hydroperitoneum | Hydroperitonia | Ascitic fluid | Peritoneal dropsy | Hydrops abdominis | Abdominal dropsy | Ascites (disorder) | Ascites (disorder) | Ascites | Hydrops abdominis | Hydroperitonia | Hydroperitoneum
+BMGC_DS00206,BMG_DS000268,,Ascorbic Acid Deficiency,Ascorbic Acid Deficiency,,,,,,C0003969,D001206,,,,
+BMGC_DS00207,BMG_DS000269,,,,,,,DOID:10159,osteonecrosis,C0003977,,,,,
+BMGC_DS00208,BMG_DS000270,65553006;154408001;266218008,Aspergillosis,Aspergillosis,,,B44,DOID:13564,aspergillosis,C0004030,D001228,,MONDO:0005657,aspergillosis,Aspergillosis | Aspergillosis (disorder) | Infection due to Aspergillus | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) | Aspergillosis | Mycoses - other | Histoplasmosis | Other mycoses | Piedra | Sporotrichosis | Coccidioidomycosis | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) (disorder) | Coccidioidomycosis | Other mycoses | Sporotrichosis | Mycoses - other | Piedra | Histoplasmosis | Aspergillosis | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) (disorder)
+BMGC_DS00209,BMG_DS000271,,"Aspergillosis, Allergic Bronchopulmonary","Aspergillosis, Allergic Bronchopulmonary",,,,DOID:13166,allergic bronchopulmonary aspergillosis,C0004031,D001229,,,,
+BMGC_DS00210,BMG_DS000273,,Asphyxia Neonatorum,Asphyxia Neonatorum,,,,DOID:11088,asphyxia neonatorum,C0004045,D001238,,MONDO:0006663,perinatal asphyxia,
+BMGC_DS00211,BMG_DS000277,187687003;155574008;278517007;21341004;195967001,Asthma,Asthma,,,J45,DOID:2841,asthma,C0004096,D001249,MTHU003537,MONDO:0004979,asthma,Asthma (disorder) | Asthma | Asthma | Asthma (disorder) | Asthmatic bronchitis | Asthma | Wheezy bronchitis | Allergic bronchitis | Asthmatic bronchitis (disorder) | Airway hyperreactivity | Asthmatic | Bronchial asthma | Bronchial hyperreactivity | BHR - Bronchial hyperreactivity | Bronchial hyperresponsiveness | Bronchial hypersensitivity | Asthma | Asthma (disorder) | Hyperreactive airway disease
+BMGC_DS00212,BMG_DS000279,82649003;155134009,Astigmatism,Astigmatism,9D00.2,Astigmatism,H52.2,DOID:11782,astigmatism,C0004106,D001251,603047;MTHU011134,MONDO:0011284,astigmatism,Astigmatism | Astigmatism (disorder)
+BMGC_DS00213,BMG_DS000280,,,,,,,DOID:3069,malignant astrocytoma,C0004114,,,MONDO:0019781,astrocytoma (excluding glioblastoma),
+BMGC_DS00214,BMG_DS000281,,Ataxia Telangiectasia,Ataxia Telangiectasia,,,,DOID:12704,ataxia telangiectasia,C0004135,D001260,208900,MONDO:0008840,ataxia telangiectasia,
+BMGC_DS00215,BMG_DS000282,,"Ataxias, Hereditary",Spinocerebellar Degenerations,,,,,,C0004138,D013132,,MONDO:0100309,hereditary ataxia,
+BMGC_DS00216,BMG_DS000283,266318005;155414001;38716007;155382007;195251000;194848007,Atherosclerosis,Atherosclerosis,,,I70,DOID:1936;DOID:2348,atherosclerosis | arteriosclerotic cardiovascular disease,C0004153,D050197,MTHU036909,MONDO:0005311,atherosclerosis,Atherosclerosis (& [NOS]) | Atherosclerosis | Arteriosclerosis NOS | Atherosclerosis (& [NOS]) (disorder) | Arteriosclerosis NOS | Atherosclerosis | Atherosclerosis (& [NOS]) | Atherosclerosis (& [NOS]) (disorder) | Atherosclerosis | Atheromatosis | Atherosclerosis (morphologic abnormality) | Atherosclerosis | Atherosclerosis (disorder) | Atherosclerotic cardiovascular disease | Arteriosclerosis | AS - Atherosclerosis | Atherosclerosis | Atherosclerosis (disorder)
+BMGC_DS00217,BMG_DS000285,44913001,Athetosis,Athetosis,,,,,,C0004158,D001264,MTHU004613,,,Athetosis | Athetosis (disorder)
+BMGC_DS00218,BMG_DS000288,,Atrial Fibrillation,Atrial Fibrillation,,,,DOID:0060224,atrial fibrillation,C0004238,D001281,,MONDO:0004981,atrial fibrillation,
+BMGC_DS00219,BMG_DS000289,,,,,,,,,C0004239,,,MONDO:0005310,atrial flutter,
+BMGC_DS00220,BMG_DS000290,,Atrioventricular Block,Atrioventricular Block,,,,DOID:0050820,atrioventricular block,C0004245,D054537,,MONDO:0000465,atrioventricular block,
+BMGC_DS00221,BMG_DS000293,,,,,,,,,C0004331,,209600,MONDO:0008848,atrioventricular dissociation,
+BMGC_DS00222,BMG_DS000294,,,,,,,DOID:12849,autistic disorder,C0004352,,209850,MONDO:0005260,autism,
+BMGC_DS00223,BMG_DS000295,,Autoimmune Diseases,Autoimmune Diseases,,,,,,C0004364,D001327,109100,MONDO:0007179,autoimmune disease,
+BMGC_DS00224,BMG_DS000296,,,,,,,DOID:1509,avoidant personality disorder,C0004444,,,MONDO:0002027,avoidant personality disorder,
+BMGC_DS00225,BMG_DS000298,167781002;145008007;198010009;155925000;48188009;425558002,Azoospermia,Azoospermia,,,N46.0,DOID:14227,azoospermia,C0004509,D053713,MTHU037275,MONDO:0100459,azoospermia,Azoospermia | Azoospermia (finding) | (Azoospermia) or (Young's syndrome) | Young's syndrome | Azoospermia | (Azoospermia) or (Young's syndrome) (disorder) | Azoospermia | Azoospermia (disorder) | Azoospermia | Azoospermatism | Azoospermia (finding) | Sperm absent - azoospermia | Sperm absent | Azoospermia disorder (disorder) | Azoospermia disorder
+BMGC_DS00226,BMG_DS000299,21061004;187241002,Babesiosis,Babesiosis,1F52,Babesiosis,B60.0,DOID:9643,babesiosis,C0004576,D001404,,MONDO:0005661,babesiosis,Babesiosis | Piroplasmosis | Babesiasis | Infection by Babesia | Red water fever | Babesiosis (disorder) | Babesiosis | Babesiosis (disorder)
+BMGC_DS00227,BMG_DS000300,390834004,Nonproliferative diabetic retinopathy,,,,,DOID:13208,background diabetic retinopathy,C0004606,,,MONDO:0001661,background diabetic retinopathy,Non proliferative diabetic retinopathy | Background diabetic retinopathy | NPDR - Non proliferative diabetic retinopathy | BDR - Background diabetic retinopathy | Nonproliferative diabetic retinopathy | Nonproliferative retinopathy due to diabetes mellitus (disorder) | Nonproliferative retinopathy due to diabetes mellitus
+BMGC_DS00228,BMG_DS000301,,,,,,,DOID:0050535,exudative vitreoretinopathy,C0004608,,,,,
+BMGC_DS00229,BMG_DS000302,,,,,,,,,C0004610,,,MONDO:0005229,bacterial infectious disease with sepsis,
+BMGC_DS00230,BMG_DS000305,,Bacterial Infections,Bacterial Infections,,,,DOID:104,bacterial infectious disease,C0004623,D001424,,MONDO:0005113,bacterial infectious disease,
+BMGC_DS00231,BMG_DS000306,,"Pneumonia, Bacterial","Pneumonia, Bacterial",,,,DOID:874,bacterial pneumonia,C0004626,D018410,,MONDO:0004652,bacterial pneumonia,
+BMGC_DS00232,BMG_DS000307,,,,,,,DOID:1412,bacteriuria,C0004659,,,MONDO:0001882,bacteriuria,
+BMGC_DS00233,BMG_DS000309,67242002,Bagassosis,Pneumoconiosis,CA70.1,Bagassosis,J67.1,DOID:12522,bagassosis,C0004681,D011009,,MONDO:0001540,bagassosis,Bagassosis | Bagasse disease | Bagasse workers' disease | Bagasse workers' lung | Sugar cane workers' hypersensitivity pneumonitis | Bagassosis (disorder)
+BMGC_DS00234,BMG_DS000310,198020004;198021000;266572002;155928003;44882003,Balanitis,Balanitis,GB06.0Z,"Balanoposthitis, unspecified",N48.1,DOID:13033,balanitis,C0004690,D001446,,MONDO:0006672,balanitis,Balanitis | Balanoposthitis | (Balanitis) or (balanoposthitis) | (Balanitis) or (balanoposthitis) (disorder) | Balanitis | Balanitis (disorder)
+BMGC_DS00235,BMG_DS000311,198020004;46090001,Balanoposthitis,,,,N47.6,DOID:13031,balanoposthitis,C0004691,,,MONDO:0001618,balanoposthitis,Balanitis | Balanoposthitis | (Balanitis) or (balanoposthitis) | (Balanitis) or (balanoposthitis) (disorder) | Balanoposthitis | Balanoposthitis (disorder)
+BMGC_DS00236,BMG_DS000312,57725006,Balantidiasis,Balantidiasis,1A30,Infections due to Balantidium coli,A07.0,DOID:12386,balantidiasis,C0004692,D001447,,MONDO:0005662,balantidiasis,Balantidiasis | Balantidiosis | Balantidial dysentery | Balantidiasis (disorder)
+BMGC_DS00237,BMG_DS000313,,Balkan Nephropathy,Balkan Nephropathy,,,,DOID:3052,Balkan nephropathy,C0004698,D001449,124100,MONDO:0007416,Balkan nephropathy,
+BMGC_DS00238,BMG_DS000314,,Balo's Concentric Sclerosis,Diffuse Cerebral Sclerosis of Schilder,,,,,,C0004712,D002549,,MONDO:0016430,Balo concentric sclerosis,
+BMGC_DS00239,BMG_DS000316,,Barrett Esophagus,Barrett Esophagus,,,,DOID:9206,Barrett's esophagus,C0004763,D001471,614266,MONDO:0013662,Barrett esophagus,
+BMGC_DS00240,BMG_DS000317,57044006,Cyst of Bartholin's gland duct,,,,,DOID:851,Bartholin's duct cyst,C0004767,,,MONDO:0004593,Bartholin duct cyst,Cyst of Bartholin's gland duct | Bartholin's gland duct cyst | Bartholin's cyst | Bartholin's gland cyst | Cyst of Bartholin's gland | Cyst of Bartholin's gland duct (disorder) | Cyst of Bartholin gland duct
+BMGC_DS00241,BMG_DS000319,,Bartonella Infections,Bartonella Infections,,,,DOID:11102,bartonellosis,C0004771,D001474,,MONDO:0005664,bartonellosis,
+BMGC_DS00242,BMG_DS000321,,Bartter Disease,Bartter Syndrome,,,,DOID:445,Bartter disease,C0004775,D001477,,MONDO:0015231,Bartter syndrome,
+BMGC_DS00243,BMG_DS000322,,,,,,,DOID:2512,nevoid basal cell carcinoma syndrome,C0004779,,,MONDO:0007187,nevoid basal cell carcinoma syndrome,
+BMGC_DS00244,BMG_DS000323,,Basal Ganglia Diseases,Basal Ganglia Diseases,,,,DOID:679,basal ganglia disease,C0004782,D001480,,,,
+BMGC_DS00245,BMG_DS000324,,Basilar Artery Insufficiency,Vertebrobasilar Insufficiency,,,,DOID:223,basilar artery insufficiency,C0004812,D014715,,MONDO:0002250,basilar artery insufficiency,
+BMGC_DS00246,BMG_DS000326,,Beckwith-Wiedemann Syndrome,Beckwith-Wiedemann Syndrome,,,,DOID:5572,Beckwith-Wiedemann syndrome,C0004903,D001506,130650,MONDO:0007534,Beckwith-Wiedemann syndrome,
+BMGC_DS00247,BMG_DS000327,,,,,,,DOID:150,disease of mental health,C0004936,,,MONDO:0005084,mental disorder,
+BMGC_DS00248,BMG_DS000328,,Behcet Syndrome,Behcet Syndrome,,,,DOID:13241,Behcet's disease,C0004943,D001528,109650,MONDO:0007191,Behcet disease,
+BMGC_DS00249,BMG_DS000329,186978001;240686008,Bejel,Treponemal Infections,,,,DOID:13431,bejel,C0004945,D014211,,MONDO:0007000;MONDO:0001714,bejel | Treponema infectious disease,Njovera | Nonvenereal endemic syphilis | Bejel | Nonvenereal endemic syphilis (& [Bejel] or [Njovera]) | Nonvenereal endemic syphilis (& [Bejel] or [Njovera]) (disorder) | Bejel | Bejel (disorder)
+BMGC_DS00250,BMG_DS000330,,,,,,,,,C0004991,,,MONDO:0002278,benign colon neoplasm,
+BMGC_DS00251,BMG_DS000334,36656008;267491008;154725000;190625009;35843007,Beriberi,Beriberi,5B5A.0Z,"Beriberi, unspecified",E51.1,DOID:13725,beriberi,C0005122,D001602,,MONDO:0006676,beriberi,Beriberi | Beriberi (disorder) | Vitamin deficiency: [thiamine/niacin] or [beriberi] or [pellagra] or [thiamine] | Pellagra | Thiamine/niacin deficiency | Beriberi | Beri-beri | Thiamine deficiency | Vitamin deficiency: [thiamine/niacin] or [beriberi] or [pellagra] or [thiamine] (disorder) | Vitamin deficiency: [thiamine/niacin] or [beriberi] or [pellagra] or [thiamine] | Beriberi | Thiamine/niacin deficiency | Beri-beri | Thiamine deficiency | Pellagra | Vitamin deficiency: [thiamine/niacin] or [beriberi] or [pellagra] or [thiamine] (disorder) | Thiamin deficiency | Chastek's paralysis | Vitamin B1 deficiency | Thiamine deficiency | Aneurin deficiency | Thiamin deficiency (disorder)
+BMGC_DS00252,BMG_DS000335,,Bernard-Soulier Syndrome,Bernard-Soulier Syndrome,,,,DOID:2217,Bernard-Soulier syndrome,C0005129,D001606,231200,MONDO:0009276,Bernard-Soulier syndrome,
+BMGC_DS00253,BMG_DS000337,,,,,,,DOID:10322,berylliosis,C0005138,,,,,
+BMGC_DS00254,BMG_DS000339,65959000,beta Thalassemia,beta-Thalassemia,,,,DOID:12241,beta thalassemia,C0005283,D017086,,MONDO:0019402,beta thalassemia,Beta thalassemia | Beta thalassemia syndrome | Beta thalassaemia syndrome | Beta thalassaemia | Beta thalassemia (disorder) | beta thalassemia | beta thalassaemia
+BMGC_DS00255,BMG_DS000340,,Bile Duct Diseases,Bile Duct Diseases,,,,DOID:4138,bile duct disease,C0005395,D001649,,MONDO:0002887,bile duct disorder,
+BMGC_DS00256,BMG_DS000341,,,,,,,DOID:4606,bile duct cancer,C0005396,,,MONDO:0021662,bile duct neoplasm,
+BMGC_DS00257,BMG_DS000342,,"Cholestasis, Extrahepatic","Cholestasis, Extrahepatic",,,,DOID:13619,extrahepatic cholestasis,C0005398,D001651,,MONDO:0006757,extrahepatic cholestasis,
+BMGC_DS00258,BMG_DS000343,,Bile Reflux,Bile Reflux,,,,DOID:12237,bile reflux,C0005403,D001655,,MONDO:0006677,bile reflux,
+BMGC_DS00259,BMG_DS000344,,,,,,,DOID:13608,biliary atresia,C0005411,,,MONDO:0008867,biliary atresia,
+BMGC_DS00260,BMG_DS000345,,Biliary Dyskinesia,Biliary Dyskinesia,,,,DOID:4140,biliary dyskinesia,C0005416,D001657,,MONDO:0005667,biliary dyskinesia,
+BMGC_DS00261,BMG_DS000346,,Biliary Tract Diseases,Biliary Tract Diseases,,,,DOID:9741,biliary tract disease,C0005424,D001660,,,,
+BMGC_DS00262,BMG_DS000347,,,,,,,DOID:4607,biliary tract cancer,C0005426,,,MONDO:0005304,biliary tract neoplasm,
+BMGC_DS00263,BMG_DS000349,83275001,Binocular vision disorder,,,,,DOID:12667,binocular vision disease,C0005461,,,MONDO:0001564,binocular vision disease,Binocular vision disorder | Binocular vision disorder (disorder)
+BMGC_DS00264,BMG_DS000350,,,,,,,DOID:3312,bipolar disorder,C0005586,,,MONDO:0004985,bipolar disorder,
+BMGC_DS00265,BMG_DS000351,,,,,,,DOID:3312,bipolar disorder,C0005587,,,MONDO:0024613,bipolar depression,
+BMGC_DS00266,BMG_DS000352,,Bird Diseases,Bird Diseases,,,,,,C0005591,D001715,,MONDO:0024905,bird disease,
+BMGC_DS00267,BMG_DS000353,,Bird Fancier's Lung,Bird Fancier's Lung,,,,DOID:13891,bird fancier's lung,C0005592,D001716,,MONDO:0005668,bird fancier's lung,
+BMGC_DS00268,BMG_DS000354,,Blackwater Fever,Blackwater Fever,,,,DOID:14068,blackwater fever,C0005681,D001742,,MONDO:0005670,blackwater fever,
+BMGC_DS00269,BMG_DS000355,70650003,Urinary bladder stone (disorder),,,,,DOID:11355,bladder calculus,C0005683,,,MONDO:0006678,bladder calculus,Urinary bladder stone | Vesical calculus | Bladder stone | Vesicolithiasis | Bladder calculus | Urinary bladder stone (disorder) | Calculus of bladder
+BMGC_DS00270,BMG_DS000356,,,,,,,DOID:11054,urinary bladder cancer,C0005684,,109800,MONDO:0001187,urinary bladder cancer,
+BMGC_DS00271,BMG_DS000357,,Urinary Bladder Diseases,Urinary Bladder Diseases,,,,DOID:365,bladder disease,C0005686,D001745,,MONDO:0006026,urinary bladder disorder,
+BMGC_DS00272,BMG_DS000358,,Bladder Exstrophy,Bladder Exstrophy,,,,DOID:0080174,bladder exstrophy,C0005689,D001746,,MONDO:0010805,bladder exstrophy,
+BMGC_DS00273,BMG_DS000359,197859007;399072004;155887006;25220001,Bladder neck obstruction,,,,,DOID:13948,bladder neck obstruction,C0005694,,,MONDO:0006679,bladder neck obstruction,Bladder neck obstruction (& [contracture] or [stenosis] or [bladder outflow obstruction]) | Contracture of bladder neck | Stenosis of bladder neck | BOO - Bladder outflow obstruction | Bladder neck obstruction | Bladder neck obstruction (& [contracture] or [stenosis] or [bladder outflow obstruction]) (disorder) | Bladder neck obstruction | Vesicourethral orifice obstruction | Obstruction of neck of urinary bladder | Obstruction of neck of urinary bladder (disorder) | BNO - bladder neck obstruction | Bladder neck obstruction | Bladder neck obstruction (disorder) | Bladder neck obstruction | Acquired bladder neck obstruction | Vesicourethral orifice obstruction | Bladder neck obstruction (disorder) | BNO - Bladder neck obstruction
+BMGC_DS00274,BMG_DS000360,,,,,,,DOID:11054,urinary bladder cancer,C0005695,,,MONDO:0004987,urinary bladder neoplasm,
+BMGC_DS00275,BMG_DS000361,,Neurogenic Urinary Bladder,"Urinary Bladder, Neurogenic",,,,DOID:12143,neurogenic bladder,C0005697,D001750,,MONDO:0001445,obsolete neurogenic bladder,
+BMGC_DS00276,BMG_DS000362,,,,,,,,,C0005699,,,MONDO:0006115,"blast phase chronic myelogenous leukemia, BCR-ABL1 positive",
+BMGC_DS00277,BMG_DS000363,69996000;187064007;154402000;266217003,Blastomycosis,Blastomycosis,,,B40,DOID:12663,blastomycosis,C0005716,D001759,,MONDO:0005672,blastomycosis,Blastomycosis | Infection by Blastomyces | Blastomycotic infection | Blastomycosis (disorder) | North American blastomycosis | Gilchrist's disease | Chicago disease | Blastomycosis (& [Chicago disease] or [Gilchrists disease] or [North American]) | Chicago disease | North American blastomycosis | Blastomycosis | Gilchrist's disease | Blastomycosis (& [Chicago disease] or [Gilchrists disease] or [North American]) (disorder) | (Other dermatophytosis) or (blastomycosis) | Blastomycosis | Other dermatophytosis | (Other dermatophytosis) or (blastomycosis) (disorder)
+BMGC_DS00278,BMG_DS000364,,Gilchrist Disease,Blastomycosis,,,,,,C0005717,D001759,,,,
+BMGC_DS00279,BMG_DS000369,193907001;155171006;155170007;193908006;41446000,Blepharitis,Blepharitis,9A01.3,Infectious blepharitis,H01.0,DOID:9423,blepharitis,C0005741,D001762,MTHU036409,MONDO:0004785,blepharitis,Blepharitis | Blepharitis (disorder) | Blepharitis (& [cellulitis of eyelids]) | Cellulitis of eyelids | Blepharitis | Blepharitis (& [cellulitis of eyelids]) (disorder) | Blepharitis | Blepharitis (disorder) | Inflammation of lid margin | Marginal blepharitis
+BMGC_DS00280,BMG_DS000370,267650003;193962005;47704002;193944001,Blepharochalasis,,9A06.8,Blepharochalasis,H02.3,DOID:348,blepharochalasis,C0005742,,MTHU037413,MONDO:0002660,blepharochalasis,Blepharochalasis | Blepharochalasis (disorder) | Blepharochalasis | Dermatolysis palpebrarum | Fuchs' syndrome II | Blepharochalasis (disorder) | (Blepharochalasis) or (pseudoptosis) | Blepharochalasis | Pseudoptosis | (Blepharochalasis) or (pseudoptosis) (disorder)
+BMGC_DS00281,BMG_DS000371,68659002;155164001,Blepharoconjunctivitis,,9A60.4,Blepharoconjunctivitis,H10.5,DOID:2456,blepharoconjunctivitis,C0005743,,MTHU070232,MONDO:0002307,blepharoconjunctivitis,Blepharoconjunctivitis | Blepharoconjunctivitis (disorder)
+BMGC_DS00282,BMG_DS000372,,,,,,,DOID:10348,blepharophimosis,C0005744,,,MONDO:0001008,blepharophimosis,
+BMGC_DS00283,BMG_DS000373,11934000;204197004,Blepharoptosis,Blepharoptosis,,,,DOID:0060260,ptosis,C0005745,D001763,MTHU000860,MONDO:0000728,ptosis,Ptosis of eyelid | Drooping eyelid | Ptosis of eyelid (disorder) | Droopy eyelid | Blepharoptosis | Ptosis | Ptosis eyelid | (Congenital ptosis) or (blepharoptosis) | Blepharoptosis | Congenital ptosis | (Congenital ptosis) or (blepharoptosis) (disorder)
+BMGC_DS00284,BMG_DS000374,59026006;155009007;267690000,Blepharospasm,Blepharospasm,8A02.00,Benign essential blepharospasm,G24.5,DOID:529,blepharospasm,C0005747,D001764,MTHU036688,,,Blepharospasm | Blepharospasm (disorder) | Spasm of eyelids | Essential blepharospasm | Benign essential blepharospasm | Blepharospasm (spasm of eyelid) | (Extrapyramidal disease NOS) or (blepharospasm) or (choreo-athetosis) or (writer's cramp - organic) or (myoclonic jerks) or (spasmodic torticollis) | Writer's cramp-organic | Writer's cramp -organic | Restless legs - organic | Organic writers' cramp | Blepharospasm | Spasmodic torticollis | Myoclonic jerks | Jerks - myoclonic | Choreo-athetosis | Organic restless legs | Extrapyramidal disease NOS | (Extrapyramidal disease NOS) or (blepharospasm) or (choreo-athetosis) or (writer's cramp - organic) or (myoclonic jerks) or (spasmodic torticollis) (disorder) | (Extrapyramidal disease NOS) or (blepharospasm) or (choreo-athetosis) or (writer's cramp - organic) or (myoclonic jerks) or (spasmodic torticollis) | Writer's cramp -organic | Writer's cramp-organic | Jerks - myoclonic | Spasmodic torticollis | Blepharospasm | Choreo-athetosis | Organic restless legs | Organic writers' cramp | Extrapyramidal disease NOS | Restless legs - organic | Myoclonic jerks | (Extrapyramidal disease NOS) or (blepharospasm) or (choreo-athetosis) or (writer's cramp - organic) or (myoclonic jerks) or (spasmodic torticollis) (disorder)
+BMGC_DS00285,BMG_DS000375,,Blind Loop Syndrome,Blind Loop Syndrome,,,,DOID:10606,blind loop syndrome,C0005750,D001765,,MONDO:0005673,blind loop syndrome,
+BMGC_DS00286,BMG_DS000376,,Blood Coagulation Disorders,Blood Coagulation Disorders,,,,DOID:1247,blood coagulation disease,C0005779,D001778,,MONDO:0001531,blood coagulation disease,
+BMGC_DS00287,BMG_DS000377,,,,,,,DOID:4176,blood group incompatibility,C0005806,,,MONDO:0002901,blood group incompatibility,
+BMGC_DS00288,BMG_DS000378,,Blood Platelet Disorders,Blood Platelet Disorders,,,,DOID:2218,blood platelet disease,C0005818,D001791,,MONDO:0000009,"inherited bleeding disorder, platelet-type",
+BMGC_DS00289,BMG_DS000379,,Blood Protein Disorders,Blood Protein Disorders,,,,DOID:620,blood protein disease,C0005830,D001796,,MONDO:0003804,obsolete blood protein disease,
+BMGC_DS00290,BMG_DS000380,,Bloom Syndrome,Bloom Syndrome,,,,DOID:2717,Bloom syndrome,C0005859,D001816,210900,MONDO:0008876,Bloom syndrome,
+BMGC_DS00291,BMG_DS000383,,Bone Diseases,Bone Diseases,,,,DOID:0080001,bone disease,C0005940,D001847,,MONDO:0005381,bone disorder,
+BMGC_DS00292,BMG_DS000384,,"Bone Diseases, Developmental","Bone Diseases, Developmental",,,,,,C0005941,D001848,,MONDO:0005497,bone development disease,
+BMGC_DS00293,BMG_DS000385,,"Bone Diseases, Endocrine","Bone Diseases, Endocrine",,,,,,C0005942,D001849,,,,
+BMGC_DS00294,BMG_DS000387,,,,,,,,,C0005944,,,MONDO:0800486,metabolic bone disorder,
+BMGC_DS00295,BMG_DS000388,,Bone Marrow Diseases,Bone Marrow Diseases,,,,DOID:4961,bone marrow disease,C0005956,D001855,,,,
+BMGC_DS00296,BMG_DS000389,,,,,,,DOID:184,bone cancer,C0005967,,,,,
+BMGC_DS00297,BMG_DS000390,,,,,,,,,C0005974,,,MONDO:0000837,bone resorption disease,
+BMGC_DS00298,BMG_DS000392,,,,,,,DOID:10930,borderline personality disorder,C0006012,,,MONDO:0001156,borderline personality disorder,
+BMGC_DS00299,BMG_DS000393,,Bordetella Infections,Bordetella Infections,,,,DOID:1116,pertussis,C0006015,D001885,,MONDO:0037872,bordetellosis,
+BMGC_DS00300,BMG_DS000394,,Borna Disease,Borna Disease,,,,DOID:5154,borna disease,C0006023,D001890,,MONDO:0005676,borna disease,
+BMGC_DS00301,BMG_DS000397,,,,,,,DOID:11976,botulism,C0006057,,,MONDO:0005498,botulism,
+BMGC_DS00302,BMG_DS000398,,Boutonneuse Fever,Boutonneuse Fever,,,,DOID:14095,boutonneuse fever,C0006060,D001907,,MONDO:0024472,boutonneuse fever,
+BMGC_DS00303,BMG_DS000400,,,,,,,,,C0006079,,,MONDO:0020761,Bowen disease of the skin,
+BMGC_DS00304,BMG_DS000401,3548001,Brachial plexus lesion,,,,,DOID:8443,brachial plexus lesion,C0006091,,,MONDO:0004569,brachial plexus neuropathy from injury,Brachial plexus lesion | Brachial plexus neuropathy | Brachial plexus disorder | BPN - Brachial plexus neuropathy | Brachial plexus disorder (disorder)
+BMGC_DS00305,BMG_DS000402,,Brain Abscess,Brain Abscess,,,,,,C0006105,D001922,,,,
+BMGC_DS00306,BMG_DS000403,,"Brain Damage, Chronic","Brain Damage, Chronic",,,,,,C0006109,D001925,,,,
+BMGC_DS00307,BMG_DS000404,,Brain Diseases,Brain Diseases,,,,DOID:936,brain disease,C0006111,D001927,,MONDO:0005560,brain disorder,
+BMGC_DS00308,BMG_DS000405,,"Brain Diseases, Metabolic","Brain Diseases, Metabolic",,,,,,C0006112,D001928,,,,
+BMGC_DS00309,BMG_DS000406,,,,,,,,,C0006114,,,MONDO:0006684,brain edema,
+BMGC_DS00310,BMG_DS000407,,,,,,,DOID:1319,brain cancer,C0006118,,,MONDO:0021211,brain neoplasm,
+BMGC_DS00311,BMG_DS000408,,Branch Retinal Artery Occlusion,Retinal Artery Occlusion,,,,DOID:13094,branch retinal artery occlusion,C0006123,D015356,,MONDO:0001630,branch retinal artery occlusion,
+BMGC_DS00312,BMG_DS000409,,,,,,,DOID:1612,breast cancer,C0006142,,,MONDO:0007254,breast cancer,
+BMGC_DS00313,BMG_DS000410,,,,,,,DOID:10350,breast cyst,C0006144,,,MONDO:0001011,breast cyst,
+BMGC_DS00314,BMG_DS000411,,Breast Diseases,Breast Diseases,,,,DOID:3463,breast disease,C0006145,D001941,,MONDO:0002657,breast disorder,
+BMGC_DS00315,BMG_DS000413,,Brill-Zinsser Disease,"Typhus, Epidemic Louse-Borne",,,,DOID:11254,Brill-Zinsser disease,C0006181,D014438,,MONDO:0005680,Brill-Zinsser disease,
+BMGC_DS00316,BMG_DS000415,,Bronchial Diseases,Bronchial Diseases,,,,DOID:1176,bronchial disease,C0006261,D001982,,MONDO:0001358,bronchial disorder,
+BMGC_DS00317,BMG_DS000416,,,,,,,DOID:3906,bronchial benign neoplasm,C0006264,,,MONDO:0002807,bronchial neoplasm,
+BMGC_DS00318,BMG_DS000417,269012003;140179000;196175000;4386001,Bronchospasm,Bronchial Spasm,,,,,,C0006266,D001986,MTHU001731,,,(Bronchospasm) or (O/E - rhonchi (& present)) | Bronchospasm | O/E - rhonchi | O/E - rhonchi present | (Bronchospasm) or (O/E - rhonchi (& present)) (finding) | Bronchospasm | Bronchospasm (disorder) | Bronchospasm | Bronchial spasm | Bronchospasm (finding)
+BMGC_DS00319,BMG_DS000418,155580000;12295008,Bronchiectasis,Bronchiectasis,,,J47,DOID:9563,bronchiectasis,C0006267,D001987,MTHU037263,MONDO:0004822,bronchiectasis,Bronchiectasis | Bronchiectasis (disorder)
+BMGC_DS00320,BMG_DS000419,4120002,Bronchiolitis,Bronchiolitis,,,,DOID:2942,bronchiolitis,C0006271,D001988,MTHU004683,MONDO:0002465,bronchiolitis,Bronchiolitis | Bronchiolitis (disorder)
+BMGC_DS00321,BMG_DS000420,,Bronchiolitis Obliterans,Bronchiolitis Obliterans,,,,DOID:2799,bronchiolitis obliterans,C0006272,D001989,,MONDO:0015265,bronchiolitis obliterans syndrome,
+BMGC_DS00322,BMG_DS000421,,"Bronchiolitis, Viral","Bronchiolitis, Viral",,,,,,C0006274,D001990,,,,
+BMGC_DS00323,BMG_DS000422,32398004,Bronchitis,Bronchitis,,,,DOID:6132,bronchitis,C0006277,D001991,MTHU004684,MONDO:0003781,bronchitis,Bronchitis | Bronchitis (disorder)
+BMGC_DS00324,BMG_DS000424,396285007;155551009;67814005,Bronchopneumonia,Bronchopneumonia,,,,DOID:12375,bronchopneumonia,C0006285,D001996,,MONDO:0005682,bronchopneumonia,Bronchopneumonia (disorder) | Bronchopneumonia | Bronchial pneumonia | Lobular pneumonia | Bronchopneumonia | Bronchopneumonia (disorder) | Bronchopneumonia | Lobular pneumonia | Segmental pneumonia | Bronchial pneumonia | Bronchopneumonia (disorder) | Bilateral bronchopneumonia
+BMGC_DS00325,BMG_DS000425,,Bronchopulmonary Dysplasia,Bronchopulmonary Dysplasia,,,,DOID:11650,bronchopulmonary dysplasia,C0006287,D001997,,MONDO:0019091,bronchopulmonary dysplasia,
+BMGC_DS00326,BMG_DS000426,75702008;154296006,Brucellosis,Brucellosis,,,A23,DOID:11077,brucellosis,C0006309,D002006,,MONDO:0005683,brucellosis,Brucellosis | Malta fever | Mediterranean fever | Undulant fever | Brucellosis (disorder) | Cyprus fever | Rock fever | Gibraltar fever | Brucellosis | Brucellosis (disorder)
+BMGC_DS00327,BMG_DS000427,,,,,,,DOID:2846,bruxism,C0006325,,,MONDO:0002443,bruxism,
+BMGC_DS00328,BMG_DS000428,,,,,,,DOID:12129,bulimia nervosa,C0006370,,,,,
+BMGC_DS00329,BMG_DS000429,,Bundle-Branch Block,Bundle-Branch Block,,,,,,C0006384,D002037,,,,
+BMGC_DS00330,BMG_DS000430,,Bunostomiasis,Hookworm Infections,,,,,,C0006389,D006725,,,,
+BMGC_DS00331,BMG_DS000433,,,,,,,DOID:8584,Burkitt lymphoma,C0006413,,113970,MONDO:0007243,Burkitt lymphoma,
+BMGC_DS00332,BMG_DS000435,,Burning Mouth Syndrome,Burning Mouth Syndrome,,,,DOID:4331,burning mouth syndrome,C0006430,D002054,,MONDO:0006687,burning mouth syndrome,
+BMGC_DS00333,BMG_DS000436,84017003;156677003,Bursitis,Bursitis,,,,DOID:2965,bursitis,C0006444,D002062,,MONDO:0002471,bursitis,Bursitis | Bursitis (disorder) | Inflammation of bursa | Bursitis | Bursitis (disorder)
+BMGC_DS00334,BMG_DS000437,155589004;266400008;85761009,Byssinosis,Byssinosis,CA80.0,Byssinosis due to exposure to cotton,J66.0,DOID:10323,byssinosis,C0006542,D002095,,MONDO:0006688,byssinosis,(Asbestosis) or (byssinosis) or (pleural plaque disease) | Pleural plaque disease | Asbestosis | Byssinosis | (Asbestosis) or (byssinosis) or (pleural plaque disease) (disorder) | Byssinosis | Asbestosis | Pleural plaque disease | (Asbestosis) or (byssinosis) or (pleural plaque disease) | (Asbestosis) or (byssinosis) or (pleural plaque disease) (disorder) | Byssinosis | Cotton workers' lung disease | Cotton-dust asthma | Byssinosis (disorder) | Mill fever
+BMGC_DS00335,BMG_DS000438,,,,,,,DOID:182,calcinosis,C0006663,,,MONDO:0002123,calcinosis,
+BMGC_DS00336,BMG_DS000440,237900002,Calciphylaxis,Calciphylaxis,,,,DOID:4734,calciphylaxis,C0006666,D002115,,MONDO:0017215,calciphylaxis,Calciphylaxis | Calciphylaxis (disorder)
+BMGC_DS00337,BMG_DS000441,,Calcium Metabolism Disorders,Calcium Metabolism Disorders,,,,DOID:10575,calcium metabolism disease,C0006705,D002128,,MONDO:0005557,calcium metabolic disease,
+BMGC_DS00338,BMG_DS000442,,,,,,,DOID:10211,cholelithiasis,C0006739,,,,,
+BMGC_DS00339,BMG_DS000445,,,,,,,DOID:13622,campylobacteriosis,C0006818,,,MONDO:0005688,campylobacteriosis,
+BMGC_DS00340,BMG_DS000446,,,,,,,DOID:162,cancer,C0006826,,,MONDO:0004992,cancer,
+BMGC_DS00341,BMG_DS000447,154403005;78048006;187005005,Candidiasis,Candidiasis,,,B37,DOID:1508,candidiasis,C0006840,D002177,MTHU042170,MONDO:0002026,candidiasis,Candidiasis | Candidiasis (disorder) | Candidiasis | Moniliasis | Candidosis | Monilia infection | Candida infection | Thrush | Candidiasis (disorder) | Infection by Candida | Candidiasis | Moniliasis | Thrush | Candidosis | Candida infection | Monilia infection | Candidiasis (disorder)
+BMGC_DS00342,BMG_DS000448,187014000,Candidiasis of skin and nails,,,,,DOID:14512,candidal paronychia,C0006842,,,,,Candidiasis of skin and nails | Candidiasis of skin and nails (disorder)
+BMGC_DS00343,BMG_DS000449,,"Candidiasis, Chronic Mucocutaneous","Candidiasis, Chronic Mucocutaneous",,,,DOID:2058,chronic mucocutaneous candidiasis,C0006845,D002178,,MONDO:0015279,chronic mucocutaneous candidiasis,
+BMGC_DS00344,BMG_DS000450,,,,,,,,,C0006846,,,MONDO:0000879,cutaneous candidiasis,
+BMGC_DS00345,BMG_DS000451,29147005,Mucocutaneous candidiasis,,,,,,,C0006848,,MTHU014262,,,Mucocutaneous candidiasis | Mucocutaneous candidiasis (disorder) | Candida infection of skin and mucous membranes
+BMGC_DS00346,BMG_DS000452,79740000;367093001;187006006,Oral candidiasis,,,,,DOID:14262,oral candidiasis,C0006849,,MTHU017529,MONDO:0005886,oral candidiasis,Candidiasis of mouth | Mycotic stomatitis | Oral candidiasis | Oral thrush | Oral moniliasis | Oral candidosis | Candidosis of mouth | Candida infection of mouth | Moniliasis of mouth | Candidiasis of mouth (disorder) | Candida of mouth | Oral candidiasis | Oral candidiasis (disorder) | Oral candidiasis | Oral moniliasis | Pharyngeal candidiasis | Candidiasis: [oral and oesophagus] or [pharyngeal] | Candidiasis: [oral and esophagus] or [pharyngeal] | Candidiasis of mouth and esophagus | Monilia of mouth and esophagus | Thrush of mouth and esophagus | Monilia of mouth and oesophagus | Candidiasis of mouth and oesophagus | Thrush of mouth and oesophagus | Candidiasis: [oral and oesophagus] or [pharyngeal] (disorder)
+BMGC_DS00347,BMG_DS000453,72934000,Candidiasis of vagina,,,,,,,C0006852,,,,,Candidiasis of vagina | Vaginal candidiasis | Candidiasis of vagina (disorder) | Vaginal thrush | Vaginal candidosis | Vaginal candida | Monilial infection of vagina | Candida of vagina
+BMGC_DS00348,BMG_DS000455,,,,,,,DOID:9505,cannabis abuse,C0006868,,,,,
+BMGC_DS00349,BMG_DS000456,,,,,,,DOID:1849,cannabis dependence,C0006870,,,MONDO:0005689,cannabis dependence,
+BMGC_DS00350,BMG_DS000457,,,,,,,DOID:6680,Capgras syndrome,C0006895,,,MONDO:0003965,Capgras syndrome,
+BMGC_DS00351,BMG_DS000458,52979002,Capillariasis,Enoplida Infections,,,,DOID:12474,capillariasis,C0006897,D017189,,MONDO:0001532;MONDO:0005745,Enoplea infectious disease | capillariasis,Capillaria infection | Capillariasis | Capillariosis | Capillaria infection (disorder)
+BMGC_DS00352,BMG_DS000461,,Caplan Syndrome,Caplan Syndrome,,,,DOID:10326,Caplan's syndrome,C0006915,D002205,,MONDO:0005690,Caplan syndrome,
+BMGC_DS00353,BMG_DS000462,,"Carbohydrate Metabolism, Inborn Errors","Carbohydrate Metabolism, Inborn Errors",,,,DOID:2978,carbohydrate metabolic disorder,C0007001,D002239,,MONDO:0019214,inborn carbohydrate metabolic disorder,
+BMGC_DS00354,BMG_DS000464,,,,,,,DOID:2176,carbuncle,C0007079,,,,,
+BMGC_DS00355,BMG_DS000467,,,,,,,DOID:305,carcinoma,C0007097,,,MONDO:0004993,carcinoma,
+BMGC_DS00356,BMG_DS000468,,,,,,,DOID:8719,in situ carcinoma,C0007099,,,MONDO:0004647,in situ carcinoma,
+BMGC_DS00357,BMG_DS000469,,,,,,,DOID:219,colon cancer,C0007102,,,MONDO:0021063,malignant colon neoplasm,
+BMGC_DS00358,BMG_DS000470,,,,,,,DOID:1380,endometrial cancer,C0007103,,608089,MONDO:0011962,endometrial cancer,
+BMGC_DS00359,BMG_DS000471,,,,,,,DOID:7843,female breast carcinoma,C0007104,,,MONDO:0004379,female breast carcinoma,
+BMGC_DS00360,BMG_DS000472,,,,,,,DOID:2596,larynx cancer,C0007107,,,MONDO:0002352,larynx cancer,
+BMGC_DS00361,BMG_DS000473,,,,,,,DOID:2526,prostate adenocarcinoma,C0007112,,,MONDO:0005082,prostate adenocarcinoma,
+BMGC_DS00362,BMG_DS000474,,,,,,,DOID:1993,rectum cancer,C0007113,,,MONDO:0044937,rectal carcinoma,
+BMGC_DS00363,BMG_DS000475,,,,,,,DOID:4159,skin cancer,C0007114,,,MONDO:0002898,skin cancer,
+BMGC_DS00364,BMG_DS000476,,,,,,,DOID:1781,thyroid cancer,C0007115,,,MONDO:0002108,thyroid cancer,
+BMGC_DS00365,BMG_DS000477,,,,,,,DOID:2513,basal cell carcinoma,C0007117,,,MONDO:0020804,basal cell carcinoma,
+BMGC_DS00366,BMG_DS000478,,,,,,,DOID:5063,basosquamous carcinoma,C0007118,,,MONDO:0003264,basosquamous carcinoma,
+BMGC_DS00367,BMG_DS000479,,,,,,,DOID:4926,bronchiolo-alveolar adenocarcinoma,C0007120,,,MONDO:0004991,minimally invasive lung adenocarcinoma,
+BMGC_DS00368,BMG_DS000480,,,,,,,DOID:3904,bronchus carcinoma,C0007121,,,MONDO:0002806,bronchogenic carcinoma,
+BMGC_DS00369,BMG_DS000481,,,,,,,,,C0007124,,,MONDO:0005023,ductal breast carcinoma in situ,
+BMGC_DS00370,BMG_DS000482,,,,,,,DOID:5050,Ehrlich tumor carcinoma,C0007125,,,MONDO:0006739,Ehrlich tumor carcinoma,
+BMGC_DS00371,BMG_DS000484,,,,,,,,,C0007129,,,MONDO:0019210,cutaneous neuroendocrine carcinoma,
+BMGC_DS00372,BMG_DS000485,,,,,,,DOID:3030,mucinous adenocarcinoma,C0007130,,,MONDO:0004957,mucinous adenocarcinoma,
+BMGC_DS00373,BMG_DS000486,,,,,,,DOID:3908,lung non-small cell carcinoma,C0007131,,,MONDO:0005233,non-small cell lung carcinoma,
+BMGC_DS00374,BMG_DS000487,,,,,,,DOID:3113,papillary carcinoma,C0007133,,,MONDO:0006509,papillary carcinoma,
+BMGC_DS00375,BMG_DS000488,,,,,,,DOID:4450,renal cell carcinoma,C0007134,,,MONDO:0005086,renal cell carcinoma,
+BMGC_DS00376,BMG_DS000489,,,,,,,DOID:4024,scirrhous adenocarcinoma,C0007135,,,MONDO:0005953,scirrhous adenocarcinoma,
+BMGC_DS00377,BMG_DS000490,,,,,,,DOID:1749,squamous cell carcinoma,C0007137,,,MONDO:0005096,squamous cell carcinoma,
+BMGC_DS00378,BMG_DS000491,,,,,,,DOID:2671,transitional cell carcinoma,C0007138,,,MONDO:0006474,transitional cell carcinoma,
+BMGC_DS00379,BMG_DS000492,,,,,,,DOID:4236,carcinosarcoma,C0007140,,,MONDO:0002928,carcinosarcoma,
+BMGC_DS00380,BMG_DS000493,,Cardiac Tamponade,Cardiac Tamponade,,,,DOID:115,cardiac tamponade,C0007177,D002305,,MONDO:0001297,cardiac tamponade,
+BMGC_DS00381,BMG_DS000494,,"Cardiomyopathy, Alcoholic","Cardiomyopathy, Alcoholic",,,,DOID:12935,alcoholic cardiomyopathy,C0007192,D002310,,MONDO:0006643,alcoholic cardiomyopathy,
+BMGC_DS00382,BMG_DS000495,,"Cardiomyopathy, Dilated","Cardiomyopathy, Dilated",,,,DOID:12930,dilated cardiomyopathy,C0007193,D002311,,MONDO:0005021,dilated cardiomyopathy,
+BMGC_DS00383,BMG_DS000496,,Hypertrophic Cardiomyopathy,"Cardiomyopathy, Hypertrophic",,,,DOID:11984,hypertrophic cardiomyopathy,C0007194,D002312,,MONDO:0005045,hypertrophic cardiomyopathy,
+BMGC_DS00384,BMG_DS000497,389996009;415295002;90828009,Restrictive cardiomyopathy,,,,,DOID:397,restrictive cardiomyopathy,C0007196,,MTHU002870,MONDO:0005201,restrictive cardiomyopathy,Restrictive cardiomyopathy | Restrictive cardiomyopathy (disorder) | Restrictive cardiomyopathy (disorder) | Restrictive cardiomyopathy | Constrictive cardiomyopathy | Primary restrictive cardiomyopathy | Primary restrictive cardiomyopathy (disorder)
+BMGC_DS00385,BMG_DS000498,,Cardiovascular Diseases,Cardiovascular Diseases,,,,DOID:1287,cardiovascular system disease,C0007222,D002318,,MONDO:0004995,cardiovascular disorder,
+BMGC_DS00386,BMG_DS000499,,Carotid Artery Diseases,Carotid Artery Diseases,,,,DOID:3407,carotid artery disease,C0007273,D002340,,MONDO:0005269,carotid artery disorder,
+BMGC_DS00387,BMG_DS000500,,Carotid Artery Thrombosis,Carotid Artery Thrombosis,,,,DOID:3410,carotid artery thrombosis,C0007274,D002341,,MONDO:0006690,carotid artery thrombosis,
+BMGC_DS00388,BMG_DS000502,,Carotid Stenosis,Carotid Stenosis,,,,DOID:13001,carotid stenosis,C0007282,D016893,,MONDO:0001612,carotid stenosis,
+BMGC_DS00389,BMG_DS000504,,Carpal Tunnel Syndrome,Carpal Tunnel Syndrome,,,,DOID:12169,carpal tunnel syndrome,C0007286,D002349,,MONDO:0007275,carpal tunnel syndrome,
+BMGC_DS00390,BMG_DS000505,,Carsickness,Motion Sickness,,,,,,C0007297,D009041,,,,
+BMGC_DS00391,BMG_DS000506,,Cartilage Diseases,Cartilage Diseases,,,,DOID:1222,cartilage disease,C0007302,D002357,,MONDO:0005569,obsolete cartilage disease,
+BMGC_DS00392,BMG_DS000507,,Cat Diseases,Cat Diseases,,,,,,C0007350,D002371,,MONDO:0024912,cat disease,
+BMGC_DS00393,BMG_DS000508,,Cat-Scratch Disease,Cat-Scratch Disease,,,,DOID:11258,cat-scratch disease,C0007361,D002372,,MONDO:0005692,cat-scratch disease,
+BMGC_DS00394,BMG_DS000509,46263000,Cataplexy,Cataplexy,,,,,,C0007384,D002385,MTHU003011,,,Cataplexy | Cataplexy (disorder)
+BMGC_DS00395,BMG_DS000511,,,,,,,,,C0007398,,,MONDO:0800105,catatonia,
+BMGC_DS00396,BMG_DS000512,,Cattle Diseases,Cattle Diseases,,,,,,C0007453,D002418,,MONDO:0024913,cattle disease,
+BMGC_DS00397,BMG_DS000514,66056001;247397004;408751001;267705008;155074001,Causalgia,Causalgia,,,,DOID:3222,causalgia,C0007462,D002422,,MONDO:0020572,complex regional pain syndrome type 2,"Causalgia | Complex regional pain syndrome type II | CRPS - Complex regional pain syndrome type II | Deafferentation pain | Causalgia (disorder) | Causalgia | Causalgia (finding) | Complex regional pain syndrome, type II (disorder) | Complex regional pain syndrome, type II | Deafferentation pain | CRPS - Complex regional pain syndrome type II | Complex regional pain syndrome type II | Causalgia | Other mononeuritis upper limb &/or causalgia | Causalgia | Other upper limb mononeuritis | Other mononeuritis -upper limb | Other mononeuritis upper limb &/or causalgia (disorder) | Other mononeuritis upper limb &/or causalgia | Other mononeuritis -upper limb | Causalgia | Other upper limb mononeuritis | Other mononeuritis upper limb &/or causalgia (disorder)"
+BMGC_DS00398,BMG_DS000515,,Cecal Diseases,Cecal Diseases,,,,DOID:1518,cecal disease,C0007527,D002429,,MONDO:0002031,cecal disorder,
+BMGC_DS00399,BMG_DS000516,,,,,,,DOID:1517,cecal benign neoplasm,C0007528,,,MONDO:0005694,cecal neoplasm,
+BMGC_DS00400,BMG_DS000517,,Celiac Disease,Celiac Disease,,,,DOID:10608,celiac disease,C0007570,D002446,,MONDO:0005130,celiac disease,
+BMGC_DS00401,BMG_DS000518,74276003;385627004;191132005;128045006,Cellulitis,Cellulitis,,,,DOID:3488,cellulitis,C0007642,D002481,MTHU034281,MONDO:0005230,cellulitis,Cellulitis | Phlegmonous cellulitis | Phlegmon | Cellulitis (morphologic abnormality) | Cellulitis (morphologic abnormality) | Cellulitis | Cellulitis | Cellulitis (disorder) | Cellulitis (disorder) | Cellulitis
+BMGC_DS00402,BMG_DS000519,,,,,,,DOID:13074,tinea unguium,C0007644,,,,,
+BMGC_DS00403,BMG_DS000521,267833003;156313004;62837005,Cellulitis of hand,,,,,DOID:3488,cellulitis,C0007646,,,,,Cellulitis of hand | Cellulitis - hand | Cellulitis of hand excluding finger | Cellulitis -hand -excl. finger | Cellulitis -hand (& -excl. finger) | Cellulitis -hand (& -excl. finger) (disorder) | Cellulitis -hand (& -excl. finger) | Cellulitis of hand excluding finger | Cellulitis - hand | Cellulitis of hand | Cellulitis -hand -excl. finger | Cellulitis -hand (& -excl. finger) (disorder) | Cellulitis of hand | Cellulitis of hand (disorder)
+BMGC_DS00404,BMG_DS000523,267144009;275539005;138748005,CNS disorder,,,,,DOID:331,central nervous system disease,C0007682,,,,,CNS disorder (& H/O) or H/O: brain disorder | H/O: CNS disorder | H/O: brain disorder | CNS disorder | CNS disorder (& H/O) or H/O: brain disorder (disorder) | CNS disorder | CNS disorder (disorder) | CNS disorder (& H/O) or H/O: brain disorder | CNS disorder | H/O: CNS disorder | H/O: brain disorder | CNS disorder (& H/O) or H/O: brain disorder (disorder)
+BMGC_DS00405,BMG_DS000524,,Central Nervous System Infection,Central Nervous System Infections,,,,,,C0007684,D002494,,,,
+BMGC_DS00406,BMG_DS000525,,Central Retinal Artery Occlusion,Retinal Artery Occlusion,,,,DOID:13098,central retinal artery occlusion,C0007688,D015356,,MONDO:0001633,central retinal artery occlusion,
+BMGC_DS00407,BMG_DS000528,,Cerebellar Ataxia,Cerebellar Ataxia,,,,DOID:0050753,cerebellar ataxia,C0007758,D002524,,MONDO:0000437,cerebellar ataxia,
+BMGC_DS00408,BMG_DS000529,,Cerebellar Diseases,Cerebellar Diseases,,,,DOID:2786,cerebellar disease,C0007760,D002526,,MONDO:0002427,cerebellar disorder,
+BMGC_DS00409,BMG_DS000530,,Myoclonic Cerebellar Dyssynergia,Myoclonic Cerebellar Dyssynergia,,,,DOID:12707,myoclonic cerebellar dyssynergia,C0007761,D002527,,,,
+BMGC_DS00410,BMG_DS000531,,,,,,,DOID:4205,cerebellum cancer,C0007762,,,MONDO:0002913,cerebellar neoplasm,
+BMGC_DS00411,BMG_DS000532,,Intracranial Aneurysm,Intracranial Aneurysm,,,,DOID:10941,intracranial aneurysm,C0007766,D002532,,,,
+BMGC_DS00412,BMG_DS000533,,Intracranial Arteriosclerosis,Intracranial Arteriosclerosis,,,,DOID:13097,intracranial arteriosclerosis,C0007771,D002537,,MONDO:0001632,intracranial arteriosclerosis,
+BMGC_DS00413,BMG_DS000534,,,,,,,DOID:0060688,arteriovenous malformations of the brain,C0007772,,,,,
+BMGC_DS00414,BMG_DS000535,28366008,Cerebral arteritis,,,,,DOID:11390,cerebral arteritis,C0007773,,,MONDO:0001277,cerebral arteritis,Cerebral arteritis | Cerebral arteritis (disorder)
+BMGC_DS00415,BMG_DS000536,,Cerebral Arterial Diseases,Cerebral Arterial Diseases,,,,DOID:3527,cerebral arterial disease,C0007774,D002539,,MONDO:0006693,cerebral arterial disease,
+BMGC_DS00416,BMG_DS000537,,Cerebral Atherosclerosis,Intracranial Arteriosclerosis,,,,DOID:12720,cerebral atherosclerosis,C0007775,D002537,,MONDO:0006694,cerebral atherosclerosis,
+BMGC_DS00417,BMG_DS000538,,Cerebral Embolism,Intracranial Embolism,,,,DOID:4372,intracranial embolism,C0007780,D020766,,,,
+BMGC_DS00418,BMG_DS000539,,Intracranial Embolism and Thrombosis,Intracranial Embolism and Thrombosis,,,,,,C0007781,D002542,,,,
+BMGC_DS00419,BMG_DS000540,,Cerebral Infarction,Cerebral Infarction,,,,DOID:3526,cerebral infarction,C0007785,D002544,,MONDO:0002679,cerebral infarction,
+BMGC_DS00420,BMG_DS000541,,Brain Ischemia,Brain Ischemia,,,,DOID:2316,brain ischemia,C0007786,D002545,,,,
+BMGC_DS00421,BMG_DS000542,,Transient Ischemic Attack,"Ischemic Attack, Transient",,,,DOID:224,transient cerebral ischemia,C0007787,D002546,,MONDO:0005264,transient ischemic attack,
+BMGC_DS00422,BMG_DS000543,16517004,Cerebral lipidosis,,,,,DOID:10742,cerebral lipidosis,C0007788,,,,,Cerebral lipidosis | Cerebral lipidosis (disorder)
+BMGC_DS00423,BMG_DS000544,,Cerebral Palsy,Cerebral Palsy,,,,DOID:1969,cerebral palsy,C0007789,D002547,,MONDO:0006497,cerebral palsy,
+BMGC_DS00424,BMG_DS000545,,Diffuse Cerebral Sclerosis of Schilder,Diffuse Cerebral Sclerosis of Schilder,,,,DOID:0060215,Balo concentric sclerosis,C0007795,D002549,272100,MONDO:0010085,Schilder disease,
+BMGC_DS00425,BMG_DS000546,,,,,,,DOID:3541,cerebral ventricle cancer,C0007798,,,MONDO:0002682,cerebral ventricle cancer,
+BMGC_DS00426,BMG_DS000547,28476005;192644005,Cerebrospinal meningitis,,,,,,,C0007813,,,,,Meningococcal meningitis | Meningococcal meningitis (disorder) | Epidemic meningitis | Cerebrospinal meningitis | Meningococcal meningitis | Meningococcal meningitis (disorder) | Meningococcal cerebrospinal fever
+BMGC_DS00427,BMG_DS000550,,Cerebrovascular Disorders,Cerebrovascular Disorders,,,,DOID:6713,cerebrovascular disease,C0007820,D002561,,MONDO:0011057,cerebrovascular disorder,
+BMGC_DS00428,BMG_DS000551,193496008,Certain types of iridocyclitis,,,,,DOID:9383,iridocyclitis,C0007832,,,,,Certain types of iridocyclitis | Certain types of iridocyclitis (disorder)
+BMGC_DS00429,BMG_DS000552,,,,,,,DOID:4362,cervical cancer,C0007847,,,,,
+BMGC_DS00430,BMG_DS000553,,Cervical Migraine Syndrome,Migraine Disorders,,,,,,C0007852,D008881,,,,
+BMGC_DS00431,BMG_DS000556,,Uterine Cervicitis,Uterine Cervicitis,,,,DOID:2568,cervicitis,C0007860,D002575,,MONDO:0002345,cervicitis,
+BMGC_DS00432,BMG_DS000557,,,,,,,DOID:2568,cervicitis,C0007861,,,,,
+BMGC_DS00433,BMG_DS000558,,Cervico-Brachial Neuralgia,Brachial Plexus Neuritis,,,,,,C0007862,D020968,,,,
+BMGC_DS00434,BMG_DS000560,,Cervix Diseases,Uterine Cervical Diseases,,,,DOID:2253,cervix disease,C0007867,D002577,,MONDO:0002256,cervix disorder,
+BMGC_DS00435,BMG_DS000562,,Cervix Erosion,Uterine Cervical Erosion,,,,DOID:3456,cervix erosion,C0007869,D002579,,,,
+BMGC_DS00436,BMG_DS000564,,,,,,,DOID:9681,cervical incompetence,C0007871,,,MONDO:0005698,cervical incompetence,
+BMGC_DS00437,BMG_DS000565,,,,,,,DOID:4362,cervical cancer,C0007873,,,MONDO:0021230,uterine cervix neoplasm,
+BMGC_DS00438,BMG_DS000569,,Meibomian Cyst,Chalazion,,,,DOID:9903,meibomian cyst,C0007933,D017043,,MONDO:0005844,chalazion,
+BMGC_DS00439,BMG_DS000570,,,,,,,DOID:4166,syphilis,C0007939,,,,,
+BMGC_DS00440,BMG_DS000572,87429008;154391003;186945008;266213004;266143009,Chancroid,Chancroid,,,A57,DOID:13778,chancroid,C0007947,D002602,,MONDO:0001797,chancroid,Chancroid | Chancroid (disorder) | Angina - Vincents | Leptospirosis | Chancroid | Weil's disease | Yaws | Vincent's angina | Trench mouth | Lymphogranuloma venereum | Spirochaete disease: [other venereal] or [Vincent's angina] or [chancroid] or [leptospirosis] or [lymphogranuloma venereum] or [trench mouth] or [Weil's disease] or [Yaws] | Other venereal/spirochaete dis | Other venereal/spirochaete disease | Spirochaete disease: [other venereal] or [Vincent's angina] or [chancroid] or [leptospirosis] or [lymphogranuloma venereum] or [trench mouth] or [Weil's disease] or [Yaws] (disorder) | (Chancroid [& bubo]) or (Ducrey's chancre) | Ducrey's chancre | Chancroid | Chancroidal bubo | (Chancroid [& bubo]) or (Ducrey's chancre) (disorder) | Other venereal/spirochaete disease | Lymphogranuloma venereum | Leptospirosis | Chancroid | Yaws | Vincent's angina | Trench mouth | Angina - Vincents | Weil's disease | Spirochaete disease: [other venereal] or [Vincent's angina] or [chancroid] or [leptospirosis] or [lymphogranuloma venereum] or [trench mouth] or [Weil's disease] or [Yaws] | Spirochaete disease: [other venereal] or [Vincent's angina] or [chancroid] or [leptospirosis] or [lymphogranuloma venereum] or [trench mouth] or [Weil's disease] or [Yaws] (disorder) | Chancroid | Soft chancre - chancroid | Chancroidal bubo | Soft sore - chancroid | Ducrey's chancre | Chancroid (disorder)
+BMGC_DS00441,BMG_DS000573,,Charcot-Marie-Tooth Disease,Charcot-Marie-Tooth Disease,,,,DOID:10595,Charcot-Marie-Tooth disease,C0007959,D002607,,MONDO:0015626,Charcot-Marie-Tooth disease,
+BMGC_DS00442,BMG_DS000574,,Chediak-Higashi Syndrome,Chediak-Higashi Syndrome,,,,DOID:2935,Chediak-Higashi syndrome,C0007965,D002609,214500,MONDO:0008963,Chediak-Higashi syndrome,
+BMGC_DS00443,BMG_DS000576,155664000;266495008;196557006;7847004,Cheilitis,Cheilitis,,,,DOID:1762,cheilitis,C0007971,D002613,MTHU068425,MONDO:0002102,cheilitis,(Oral soft tissue diseases NOS) or (canker) or (cheilitis) or (mucocele of mouth) | Oral soft tissue disease NOS | Cheilitis | Mucocele of mouth | Canker | Oral soft tissue diseases NOS | Mucocele - mouth | (Oral soft tissue diseases NOS) or (canker) or (cheilitis) or (mucocele of mouth) (disorder) | (Oral soft tissue diseases NOS) or (canker) or (cheilitis) or (mucocele of mouth) | Canker | Oral soft tissue diseases NOS | Cheilitis | Mucocele of mouth | Oral soft tissue disease NOS | Mucocele - mouth | (Oral soft tissue diseases NOS) or (canker) or (cheilitis) or (mucocele of mouth) (disorder) | Cheilitis | Cheilitis (disorder)
+BMGC_DS00444,BMG_DS000577,76098004;53432004,Cherubism,Cherubism,,,M27.8,DOID:1856,cherubism,C0008029,D002636,MTHU073148;118400,MONDO:0007315,cherubism,Fibrous dysplasia of jaw | Fibrous dysplasia of jaw (disorder) | Cherubism | Familial fibrous dysplasia of jaw | Cherubism | Familial fibrous dysplasia of jaw | Cherubism (disorder) | Familial multilocular cystic disease of the jaws
+BMGC_DS00445,BMG_DS000578,,Chiari-Frommel Syndrome,Chiari-Frommel Syndrome,,,,DOID:12700,hyperprolactinemia,C0008043,D002640,,MONDO:0043226,postpartum amenorrhea-galactorrhea syndrome,
+BMGC_DS00446,BMG_DS000579,186508005;38907003,Chickenpox,Chickenpox,,,,DOID:8659,chickenpox,C0008049,D002644,,MONDO:0005700,chickenpox,Varicella infection (& [chickenpox]) | Chickenpox | Chickenpox - varicella | Varicella infection (& [chickenpox]) (disorder) | Varicella | Chickenpox | Varicella infection | Chicken pox | Varicella (disorder)
+BMGC_DS00447,BMG_DS000580,,Chikungunya Fever,Chikungunya Fever,,,,,,C0008055,D065632,,MONDO:0017941,chikungunya,
+BMGC_DS00448,BMG_DS000581,,Child Nutrition Disorders,Child Nutrition Disorders,,,,,,C0008087,D015362,,,,
+BMGC_DS00449,BMG_DS000582,,Glutamate Monosodium Sensitivity,,,,,,,C0008127,C562377,231630,MONDO:0009280,monosodium glutamate sensitivity,
+BMGC_DS00450,BMG_DS000583,,Chlamydia Infections,Chlamydia Infections,,,,,,C0008149,D002690,,MONDO:0005701,chlamydia trachomatis infectious disease,
+BMGC_DS00451,BMG_DS000585,191125001;87522002,Asiderotic anemia,,,,,,,C0008272,,,,,Deficiency anemiasm (& [asiderotic] or [sideropenic]) | Asiderotic anemia | Deficiency anemias | Sideropenic anemia | Deficiency anaemias | Sideropenic anaemia | Asiderotic anaemia | Deficiency anaemiasm (& [asiderotic] or [sideropenic]) | Deficiency anaemiasm (& [asiderotic] or [sideropenic]) (disorder) | Iron deficiency anemia | Asiderotic anemia | Chlorotic anemia | Sideropenic anemia | Iron deficiency anaemia | IDA - Iron deficiency anemia | Iron deficiency anemia syndrome | Asiderotic anaemia | IDA - Iron deficiency anaemia | Sideropenic anaemia | Iron deficiency anaemia syndrome | Chlorotic anaemia | Iron deficiency anemia (disorder)
+BMGC_DS00452,BMG_DS000586,,,,,,,DOID:9574,choanal atresia,C0008297,,608911,MONDO:0012155,choanal atresia,
+BMGC_DS00453,BMG_DS000588,,,,,,,DOID:5381,bile duct adenoma,C0008309,,,MONDO:0006108,bile duct adenoma,
+BMGC_DS00454,BMG_DS000589,82403002;155831003,Cholangitis,Cholangitis,DC13,Cholangitis,K83.0,DOID:9446,cholangitis,C0008311,D002761,MTHU036659,MONDO:0004789,cholangitis,Cholangitis | Cholangitis (disorder)
+BMGC_DS00455,BMG_DS000590,,Primary Biliary Cholangitis,"Liver Cirrhosis, Biliary",,,,DOID:12236,primary biliary cholangitis,C0008312,D008105,,MONDO:0005388,primary biliary cholangitis,
+BMGC_DS00456,BMG_DS000591,,"Cholangitis, Sclerosing","Cholangitis, Sclerosing",,,,DOID:14268,sclerosing cholangitis,C0008313,D015209,,MONDO:0018646,sclerosing cholangitis,
+BMGC_DS00457,BMG_DS000592,76581006,Cholecystitis,Cholecystitis,,,K81,DOID:1949,cholecystitis,C0008325,D002764,MTHU009746,MONDO:0002155,cholecystitis,Cholecystitis | Cholecystitis (disorder) | Inflamed gallbladder
+BMGC_DS00458,BMG_DS000593,,,,,,,DOID:899,choledochal cyst,C0008340,,603003,MONDO:0018805,bile duct cyst,
+BMGC_DS00459,BMG_DS000594,44900007;197376000;266541001;155823008;266474003,Cholelithiasis,Cholelithiasis,,,K80,,,C0008350,D002769,MTHU009745;611465,MONDO:0012672,cholelithiasis,Biliary calculus | Biliary calculus (disorder) | Cholelithiasis (& calculus: [bile duct] or [cystic duct] or [gallbladder]) | Cholelithiasis | Bile duct calculus | Calculus - biliary | Gallstones | Gallbladder calculus | Cystic duct calculus | Stone - biliary | Gall stones (& [calculus - gall bladder]) | Stones - gall | Gallbladder calculus | Calculus - gall bladder | Gallstones | Cholelithiasis | Gallstones | Gallbladder calculus | Cholelithiasis | Calculus - gall bladder | Stones - gall | Gall stones (& [calculus - gall bladder]) | Biliary calculus | Cholelithiasis | CL - Cholelithiasis | Stone - biliary | Calculus - biliary | Calculus in biliary tract | Calculus in biliary tract (disorder)
+BMGC_DS00460,BMG_DS000595,63650001;154269008;186087007,Cholera,Cholera,,,A00,DOID:1498,cholera,C0008354,D002771,,MONDO:0015766,cholera,Cholera | Cholera (disorder) | Vibrio cholerae infection | Cholera | Cholera (disorder) | Vibrio cholerae | Cholera | (Cholera) or (Vibrio cholerae) | (Cholera) or (Vibrio cholerae) (disorder)
+BMGC_DS00461,BMG_DS000596,33688009,Cholestasis,Cholestasis,,,,DOID:13580,cholestasis,C0008370,D002779,MTHU001311,MONDO:0001751,cholestasis,Cholestasis | Bile stasis | Cholestasis (finding)
+BMGC_DS00462,BMG_DS000597,,Intrahepatic Cholestasis,"Cholestasis, Intrahepatic",,,,DOID:1852,intrahepatic cholestasis,C0008372,D002780,,MONDO:0019072,intrahepatic cholestasis,
+BMGC_DS00463,BMG_DS000598,267766007;575006;363668000;155244001,Cholesteatoma,Cholesteatoma,,,,DOID:869,cholesteatoma,C0008373,D002781,MTHU063971,MONDO:0006530,cholesteatoma,(Cholesteatoma middle ear) or (middle ear polyp) | Polyp of middle ear | Polyp - middle ear | Cholesteatoma | Cholesteatoma-polyp.-middle e. | (Cholesteatoma middle ear) or (middle ear polyp) (disorder) | Cholesteatoma | Epidermoid cholesteatoma | Cholesteatoma (morphologic abnormality) | Cholesteatoma | Cholesteatoma (disorder) | Cholesteatoma pearl | (Cholesteatoma middle ear) or (middle ear polyp) | Polyp of middle ear | Polyp - middle ear | Cholesteatoma-polyp.-middle e. | Cholesteatoma | (Cholesteatoma middle ear) or (middle ear polyp) (disorder)
+BMGC_DS00464,BMG_DS000599,39911004;194339007,Cholesteatoma of middle ear and mastoid,,,,,DOID:10964,cholesteatoma of middle ear,C0008374,,,,,Cholesteatoma of middle ear / mastoid | Cholesteatoma of middle ear and mastoid structure (disorder) | Cholesteatoma of middle ear and mastoid structure | Cholesteatoma of middle ear and mastoid | Cholesteatoma of middle ear and mastoid (disorder)
+BMGC_DS00465,BMG_DS000600,,Cholesterol Ester Storage Disease,Cholesterol Ester Storage Disease,,,,DOID:14502,cholesterol ester storage disease,C0008384,D015217,278000,MONDO:0019149,cholesteryl ester storage disease,
+BMGC_DS00466,BMG_DS000601,,Choline Deficiency,Choline Deficiency,,,,DOID:8456,choline deficiency disease,C0008412,D002796,,MONDO:0004575,choline deficiency disease,
+BMGC_DS00467,BMG_DS000602,,,,,,,DOID:2649,chondroblastoma,C0008441,,,MONDO:0004997,chondroblastoma,
+BMGC_DS00468,BMG_DS000603,,Chondrodysplasia Punctata,Chondrodysplasia Punctata,,,,DOID:2581,chondrodysplasia punctata,C0008445,D002806,,MONDO:0019701,chondrodysplasia punctata,
+BMGC_DS00469,BMG_DS000604,67988000,Congenital anomaly of cartilage,,,,,DOID:2256,osteochondrodysplasia,C0008449,,,MONDO:0020779,cartilage development disorder,Congenital anomaly of cartilage | Chondrodystrophy | Abnormal development of cartilage | Congenital anomaly of cartilage (disorder)
+BMGC_DS00470,BMG_DS000605,,Chondromalacia Patellae,Chondromalacia Patellae,,,,DOID:13357,chondromalacia patellae,C0008475,D046789,168900,MONDO:0008207,chondromalacia patellae,
+BMGC_DS00471,BMG_DS000607,,,,,,,DOID:3371,chondrosarcoma,C0008479,,215300,MONDO:0008977,chondrosarcoma,
+BMGC_DS00472,BMG_DS000608,,,,,,,DOID:3302,chordoma,C0008487,,215400,MONDO:0008978,chordoma,
+BMGC_DS00473,BMG_DS000609,5027007;271700006,Chorea,Chorea,,,,,,C0008489,D002819,MTHU003622,MONDO:0001595,choreatic disease,Chorea | Chorea (disorder) | Chorea | Choreiform movement | Choreic movement | Chorea (disorder) | Choreiform disorder
+BMGC_DS00474,BMG_DS000611,267263003;199675000;11612004,Chorioamnionitis,Chorioamnionitis,,,O41.12,DOID:0050697,chorioamnionitis,C0008495,D002821,,MONDO:0000409,chorioamnionitis,Chorioamnionitis | Chorioamnionitis (disorder) | Amniotic cavity infection (& [membranitis] or [placentitis]) | Amnionitis | Membranitis | Placentitis | Amniotic cavity infection | Chorioamnionitis | Amniotic cavity infection (& [membranitis] or [placentitis]) (disorder) | Chorioamnionitis | Membranitis | Chorioamnionitis (disorder)
+BMGC_DS00475,BMG_DS000612,,,,,,,DOID:3594,choriocarcinoma,C0008497,,,MONDO:0005207,choriocarcinoma,
+BMGC_DS00476,BMG_DS000613,,,,,,,DOID:11086,chorioretinal scar,C0008512,,,,,
+BMGC_DS00477,BMG_DS000614,270531006;46627006,Chorioretinitis,Chorioretinitis,,,,DOID:8886,chorioretinitis,C0008513,D002825,MTHU058287,MONDO:0004674,chorioretinitis,Photoretinitis | Chorioretinitis | Chorioretinitis (& photoretinitis) | Chorioretinitis (& photoretinitis) (disorder) | Chorioretinitis | Chorioretinal inflammation | Choroiditis and retinitis | Retinochoroiditis | Chorioretinitis (disorder)
+BMGC_DS00478,BMG_DS000615,,Choroid Diseases,Choroid Diseases,,,,DOID:1417,choroid disease,C0008521,D015862,,,,
+BMGC_DS00479,BMG_DS000616,,,,,,,DOID:12759,choroid cancer,C0008523,,,MONDO:0021258,choroid neoplasm,
+BMGC_DS00480,BMG_DS000617,75241009,Choroideremia,Choroideremia,,,H31.21,DOID:9821,choroideremia,C0008525,D015794,303100,MONDO:0010557,choroideremia,Choroideremia | Choroideraemia | Choroideremia (disorder) | Tapetochoroidal dystrophy
+BMGC_DS00481,BMG_DS000618,16553002,Choroiditis,Choroiditis,,,,DOID:11406,choroiditis,C0008526,D002833,MTHU069070,MONDO:0001280,choroiditis,Choroiditis | Choroiditis (disorder)
+BMGC_DS00482,BMG_DS000619,41788008,Hemophilia B,Hemophilia B,,,D67,DOID:12259,hemophilia B,C0008533,D002836,306900,MONDO:0010604,hemophilia B,Hemophilia B | Hereditary factor IX deficiency disease | Christmas disease | Sex-linked factor IX deficiency disease | PTC deficiency disease | Haemophilia B | Congenital factor IX deficiency | Hereditary factor IX deficiency disease (disorder)
+BMGC_DS00483,BMG_DS000620,187079000;7255004,Chromoblastomycosis,Chromoblastomycosis,,,,DOID:1562,chromoblastomycosis,C0008582,D002862,,MONDO:0015908,chromomycosis,Chromoblastomycosis | Chromoblastomycosis (disorder) | Chromomycosis | Chromomycosis | Chromomycosis (disorder)
+BMGC_DS00484,BMG_DS000622,74345006,Congenital chromosomal disease,,,,,,,C0008626,,,MONDO:0019040,chromosomal disorder,Chromosomopathy | Chromosomal abnormality syndrome | Chromosomal hereditary disorder | Chromosomal imbalance syndrome | Anomaly of chromosome | Congenital chromosomal disease | Congenital disorder due to abnormality of chromosome number OR structure (disorder) | Congenital disorder due to abnormality of chromosome number OR structure
+BMGC_DS00485,BMG_DS000623,,"Bronchitis, Chronic","Bronchitis, Chronic",,,,DOID:6132,bronchitis,C0008677,D029481,,MONDO:0005607,chronic bronchitis,
+BMGC_DS00486,BMG_DS000625,233692000,Cryptogenic pulmonary eosinophilia,,,,,DOID:9502,chronic eosinophilic pneumonia,C0008680,,,MONDO:0004806,chronic eosinophilic pneumonia,Cryptogenic pulmonary eosinophilia | Chronic pulmonary eosinophilia | Cryptogenic pulmonary eosinophilia (disorder) | Idiopathic pulmonary eosinophilia | Cryptogenic eosinophilic pneumonitis | Chronic eosinophilic pneumonitis
+BMGC_DS00487,BMG_DS000626,73237007;266384001;155528009,Chronic ethmoidal sinusitis,,XA58F6;CA0A.Y,Ethmoid sinus | Other specified chronic rhinosinusitis,J32.2,DOID:9312,chronic ethmoiditis,C0008681,,,MONDO:0004757,chronic ethmoidal sinusitis,"Chronic ethmoidal sinusitis | Chronic ethmoidal sinusitis (disorder) | Chronic ethmoiditis | Chronic sinusitis: [NOS] or [ethmoidal] or [chronic pansinusitis] or [sphenoidal] | Chronic pansinusitis | Chronic sinusitis NOS | Chronic ethmoidal sinusitis | Chronic sphenoidal sinusitis | Ethmoidal sinusitis - chronic | Pansinusitis, chronic | Sphenoidal sinus-chr. | Chronic sinusitis: [NOS] or [ethmoidal] or [chronic pansinusitis] or [sphenoidal] (disorder) | Chronic sinusitis: [NOS] or [ethmoidal] or [chronic pansinusitis] or [sphenoidal] | Chronic pansinusitis | Sphenoidal sinus-chr. | Chronic sphenoidal sinusitis | Ethmoidal sinusitis - chronic | Chronic ethmoidal sinusitis | Pansinusitis, chronic | Chronic sinusitis NOS | Chronic sinusitis: [NOS] or [ethmoidal] or [chronic pansinusitis] or [sphenoidal] (disorder)"
+BMGC_DS00488,BMG_DS000627,155527004;195786002;60130002,Chronic frontal sinusitis,,XA91G8;CA0A.Y,Frontal sinus | Other specified chronic rhinosinusitis,J32.1,DOID:10790,chronic frontal sinusitis,C0008683,,,MONDO:0001120,chronic frontal sinusitis,Chronic frontal sinusitis | Chronic frontal sinusitis (disorder) | Chronic frontal sinusitis | Frontal sinusitis | Frontal sinusitis (& chronic) | Frontal sinusitis (& chronic) (disorder)
+BMGC_DS00489,BMG_DS000628,266490003;155644005;72621003;196355002,Chronic gingivitis,,DA0Z,"Diseases or disorders of orofacial complex, unspecified",K05.1,DOID:3087,gingivitis,C0008684,,,MONDO:0020782,chronic gingivitis,(Chronic gingivitis) or (gingivostomatitis) | Gingivostomatitis | Chronic gingivitis | (Chronic gingivitis) or (gingivostomatitis) (disorder) | Chronic gingivitis | Chronic gingivitis (disorder) | Gingivitis | Chronic gingivitis | Gingivitis (& [chronic]) | Gingivitis (& [chronic]) (disorder)
+BMGC_DS00490,BMG_DS000630,195785003;155526008;35923002,Chronic maxillary sinusitis,,CA0A.Y;XA1R64,Other specified chronic rhinosinusitis | Maxillary sinus,J32.0,DOID:10792,chronic maxillary sinusitis,C0008698,,,MONDO:0001122,chronic maxillary sinusitis,(Maxillary sinusitis) or (chronic antritis) | Chronic maxillary sinusitis | Antritis - chronic | Chronic antritis | Maxillary sinusitis | (Maxillary sinusitis) or (chronic antritis) (disorder) | Chronic maxillary sinusitis | Chronic maxillary sinusitis (disorder) | Chronic maxillary sinusitis | Chronic antritis | Chronic maxillary sinusitis (disorder)
+BMGC_DS00491,BMG_DS000631,,,,,,,DOID:10600,chronic tic disorder,C0008701,,,MONDO:0001074,chronic tic disorder,
+BMGC_DS00492,BMG_DS000632,203181001;156791003;40970001,Chronic osteomyelitis,,,,,DOID:1019,osteomyelitis,C0008707,,,,,(Osteomyelitis: [chronic] or [Garre's sclerosing]) or (Brodie's abscess) or (sequestrum of bone) | Chronic osteomyelitis | Garre's sclerosing osteomyelitis | Brodie's abscess | Sequestrum of bone | (Osteomyelitis: [chronic] or [Garre's sclerosing]) or (Brodie's abscess) or (sequestrum of bone) (disorder) | Chronic osteomyelitis | Chronic osteomyelitis (disorder)
+BMGC_DS00493,BMG_DS000633,270532004;195764003;86094006;155522005,Chronic rhinitis,,CA09.0,Chronic rhinitis,J31.0,DOID:8252,chronic rhinitis,C0008711,,MTHU039707,MONDO:0004514,chronic rhinitis,Chronic rhinitis (& ozaena) | Chronic rhinitis | Ozena | Ozaena | Rhinitis - chronic | Chronic rhinitis (& ozaena) (disorder) | (Chronic rhinitis) or (catarrh unspecified) | Chronic rhinitis | Catarrh unspecified | (Chronic rhinitis) or (catarrh unspecified) (disorder) | Chronic rhinitis | Chronic rhinitis (disorder) | Chronic rhinitis | Rhinitis - chronic | Ozena | Ozaena | Chronic rhinitis (& ozaena) | Chronic rhinitis (& ozaena) (disorder)
+BMGC_DS00494,BMG_DS000634,38961000;266384001;155528009,Chronic sphenoidal sinusitis,,XA4U67;CA0A.Y,Sphenoid sinus | Other specified chronic rhinosinusitis,J32.3,DOID:10793,chronic sphenoidal sinusitis,C0008712,,,MONDO:0001123,chronic sphenoidal sinusitis,"Chronic sphenoidal sinusitis | Chronic sphenoidal sinusitis (disorder) | Chronic sinusitis: [NOS] or [ethmoidal] or [chronic pansinusitis] or [sphenoidal] | Chronic pansinusitis | Chronic sinusitis NOS | Chronic ethmoidal sinusitis | Chronic sphenoidal sinusitis | Ethmoidal sinusitis - chronic | Pansinusitis, chronic | Sphenoidal sinus-chr. | Chronic sinusitis: [NOS] or [ethmoidal] or [chronic pansinusitis] or [sphenoidal] (disorder) | Chronic sinusitis: [NOS] or [ethmoidal] or [chronic pansinusitis] or [sphenoidal] | Chronic pansinusitis | Sphenoidal sinus-chr. | Chronic sphenoidal sinusitis | Ethmoidal sinusitis - chronic | Chronic ethmoidal sinusitis | Pansinusitis, chronic | Chronic sinusitis NOS | Chronic sinusitis: [NOS] or [ethmoidal] or [chronic pansinusitis] or [sphenoidal] (disorder)"
+BMGC_DS00495,BMG_DS000635,,Chronically Ill,Chronic Disease,,,,,,C0008715,D002908,,,,
+BMGC_DS00496,BMG_DS000636,82275008,Eosinophilic granulomatosis with polyangiitis,,,,,DOID:3049,Churg-Strauss syndrome,C0008728,,,MONDO:0015943,eosinophilic granulomatosis with polyangiitis,Allergic granulomatosis angiitis | Churg-Strauss syndrome | Allergic granulomatosis angiitis (disorder) | Allergic granulomatous angiitis | CSS - Churg-Strauss syndrome | Churg Strauss syndrome | Eosinophilic granulomatosis with polyangiitis | EGPA - eosinophilic granulomatosis with polyangiitis
+BMGC_DS00497,BMG_DS000637,,Chylous Ascites,Chylous Ascites,,,,,,C0008732,D002915,208300,MONDO:0008829,chylous ascites,
+BMGC_DS00498,BMG_DS000638,83035003;196093002,Chylothorax,Chylothorax,,,,,,C0008733,D002916,MTHU009832,,,Chylothorax | Chylothorax (disorder)
+BMGC_DS00499,BMG_DS000639,,Ciliary Motility Disorders,Ciliary Motility Disorders,,,,DOID:9562,primary ciliary dyskinesia,C0008780,D002925,,MONDO:0016575,primary ciliary dyskinesia,
+BMGC_DS00500,BMG_DS000640,19943007,Cirrhosis of liver without mention of alcohol,,,,,,,C0008827,,,,,Cirrhosis of liver | Hepatic cirrhosis | CL - Cirrhosis of liver | Cirrhosis of liver (disorder)
+BMGC_DS00501,BMG_DS000641,,,,,,,DOID:9296,cleft lip,C0008924,,,MONDO:0016043,isolated cleft lip,
+BMGC_DS00502,BMG_DS000642,,,,,,,DOID:674,cleft palate,C0008925,,,,,
+BMGC_DS00503,BMG_DS000643,,Cleidocranial Dysplasia,Cleidocranial Dysplasia,,,,DOID:13994,cleidocranial dysplasia,C0008928,D002973,119600,MONDO:0007340,cleidocranial dysplasia 1,
+BMGC_DS00504,BMG_DS000644,11938002,Clonorchiasis,Clonorchiasis,1F80,Clonorchiasis,B66.1,DOID:13767,clonorchiasis,C0009021,D003003,,MONDO:0005705,clonorchiasis,Clonorchiasis | Chinese liver fluke disease | Oriental liver fluke disease | Hepatic distomiasis due to Clonorchis sinensis | Clonorchiosis | Clonorchiasis (disorder)
+BMGC_DS00505,BMG_DS000646,,,,,,,DOID:11836,clubfoot,C0009081,,119800,MONDO:0007342,clubfoot,
+BMGC_DS00506,BMG_DS000647,,Cluster Headache,Cluster Headache,,,,,,C0009088,D003027,,MONDO:0043537,cluster headache syndrome,
+BMGC_DS00507,BMG_DS000648,,,,,,,DOID:809,cocaine abuse,C0009171,,,MONDO:0004456,cocaine abuse,
+BMGC_DS00508,BMG_DS000649,266218008;60826002;154408001;187025009,Coccidioidomycosis,Coccidioidomycosis,,,B38,DOID:13450,coccidioidomycosis,C0009186,D003047,,MONDO:0005706,coccidioidomycosis,Coccidioidomycosis | Other mycoses | Sporotrichosis | Mycoses - other | Piedra | Histoplasmosis | Aspergillosis | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) (disorder) | Coccidioidomycosis | Posadas-Wernicke disease | Coccidioidomycosis (disorder) | Coccidioidomycosis infection | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) | Aspergillosis | Mycoses - other | Histoplasmosis | Other mycoses | Piedra | Sporotrichosis | Coccidioidomycosis | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) (disorder) | Coccidioidomycosis | Coccidioidomycosis (disorder)
+BMGC_DS00509,BMG_DS000650,62005008;186125004,Coccidiosis,Coccidiosis,,,,DOID:2113,coccidiosis,C0009187,D003048,,MONDO:0005707,coccidiosis,Coccidiosis | Coccidiosis (disorder) | Coccidiosis infection | Coccidiosis | Coccidiosis (& [intestinal]) | Coccidiosis (& [intestinal]) (disorder)
+BMGC_DS00510,BMG_DS000652,,Cochlear Diseases,Cochlear Diseases,,,,DOID:5463,cochlear disease,C0009197,D015834,,MONDO:0003452,cochlear disorder,
+BMGC_DS00511,BMG_DS000653,,Cockayne Syndrome,Cockayne Syndrome,,,,DOID:2962,Cockayne syndrome,C0009207,D003057,,MONDO:0016006,Cockayne syndrome,
+BMGC_DS00512,BMG_DS000657,308689002,Coin lesion of lung,,,,,DOID:5364,pulmonary coin lesion,C0009250,,,MONDO:0006931,pulmonary coin lesion,Coin lesion of lung | Coin lesion of lung (finding)
+BMGC_DS00513,BMG_DS000658,,Cold Panniculitis,Panniculitis,,,,,,C0009270,D015434,,,,
+BMGC_DS00514,BMG_DS000659,64226004,Colitis,Colitis,,,,DOID:0060180,colitis,C0009319,D003092,MTHU036324,MONDO:0005292,colitis,Colitis | Colitis (disorder) | Colon inflammation
+BMGC_DS00515,BMG_DS000660,,Ulcerative Colitis,"Colitis, Ulcerative",,,,DOID:8577,ulcerative colitis,C0009324,D003093,,MONDO:0005101,ulcerative colitis,
+BMGC_DS00516,BMG_DS000661,,Collagen Diseases,Collagen Diseases,,,,DOID:854,collagen disease,C0009326,D003095,,MONDO:0005554;MONDO:0021103,obsolete collagen diseases | rheumatic disorder,
+BMGC_DS00517,BMG_DS000662,,,,,,,DOID:12270,coloboma,C0009363,,,MONDO:0001476,coloboma,
+BMGC_DS00518,BMG_DS000663,,Colonic Diseases,Colonic Diseases,,,,DOID:5353,colonic disease,C0009373,D003108,,MONDO:0003409,colonic disorder,
+BMGC_DS00519,BMG_DS000664,,"Colonic Diseases, Functional","Colonic Diseases, Functional",,,,DOID:3877,functional colonic disease,C0009374,D003109,,MONDO:0002802,functional colonic disease,
+BMGC_DS00520,BMG_DS000665,,,,,,,DOID:235,colonic benign neoplasm,C0009375,,,MONDO:0005401,colonic neoplasm,
+BMGC_DS00521,BMG_DS000666,,,,,,,,,C0009376,,,MONDO:0021400,polyp of colon,
+BMGC_DS00522,BMG_DS000667,,Colonic Pseudo-Obstruction,Colonic Pseudo-Obstruction,,,,DOID:3876,colonic pseudo-obstruction,C0009377,D003112,,MONDO:0002801,colonic pseudo-obstruction,
+BMGC_DS00523,BMG_DS000668,,Colorado Tick Fever,Colorado Tick Fever,,,,DOID:4885,Colorado tick fever,C0009400,D003121,,MONDO:0005708,Colorado tick fever,
+BMGC_DS00524,BMG_DS000669,,,,,,,DOID:0080199,colorectal carcinoma,C0009402,,,MONDO:0024331,colorectal carcinoma,
+BMGC_DS00525,BMG_DS000670,,,,,,,DOID:9256,colorectal cancer,C0009404,,,MONDO:0005335,colorectal neoplasm,
+BMGC_DS00526,BMG_DS000671,,,,,,,DOID:3883,Lynch syndrome,C0009405,,,,,
+BMGC_DS00527,BMG_DS000672,50061006;371632003,Comatose,Coma,,,,,,C0009421,D003128,,,,Coma | Exanimation | Comatose | Coma (finding) | Coma (disorder) | Coma | Comatose | Exanimation
+BMGC_DS00528,BMG_DS000673,,,,,,,DOID:6950,combat disorder,C0009426,,,MONDO:0004049,combat disorder,
+BMGC_DS00529,BMG_DS000674,,Common Bile Duct Diseases,Common Bile Duct Diseases,,,,DOID:4137,common bile duct disease,C0009440,D003137,,MONDO:0002886,common bile duct disorder,
+BMGC_DS00530,BMG_DS000675,,,,,,,DOID:4608,common bile duct neoplasm,C0009442,,,MONDO:0006709,common bile duct neoplasm,
+BMGC_DS00531,BMG_DS000676,,Common Cold,Common Cold,,,,DOID:10459,common cold,C0009443,D003139,,MONDO:0005709,common cold,
+BMGC_DS00532,BMG_DS000677,,Common Variable Immunodeficiency,Common Variable Immunodeficiency,,,,DOID:12177,common variable immunodeficiency,C0009447,D017074,,MONDO:0015517,common variable immunodeficiency,
+BMGC_DS00533,BMG_DS000678,,Communicable Diseases,Communicable Diseases,,,,,,C0009450,D003141,,MONDO:0005550,infectious disease,
+BMGC_DS00534,BMG_DS000679,,Communicating Hydrocephalus,Hydrocephalus,,,,DOID:1573,communicating hydrocephalus,C0009451,D006849,,MONDO:0002045,communicating hydrocephalus,
+BMGC_DS00535,BMG_DS000680,,,,,,,DOID:2033,communication disorder,C0009460,,,MONDO:0002182,communication disorder,
+BMGC_DS00536,BMG_DS000681,,,,,,,DOID:682,compartment syndrome,C0009492,,,MONDO:0004001,compartment syndrome,
+BMGC_DS00537,BMG_DS000682,46963008,Compression of brain,,KB07,Compression of brain in neonate,G93.5,DOID:11457,brain compression,C0009592,,,MONDO:0001291,brain compression,Compression of brain | Compression of brain (disorder)
+BMGC_DS00538,BMG_DS000683,,,,,,,DOID:10932,obsessive-compulsive personality disorder,C0009595,,,MONDO:0001158,obsessive-compulsive personality disorder,
+BMGC_DS00539,BMG_DS000684,,Condylomata Acuminata,Condylomata Acuminata,,,,DOID:11168,anogenital venereal wart,C0009663,D003218,,,,
+BMGC_DS00540,BMG_DS000685,,,,,,,,,C0009677,,153630,MONDO:0007927,congenital macroglossia,
+BMGC_DS00541,BMG_DS000688,,"Hepatic Fibrosis, Congenital",,,,,,,C0009714,C562378,,MONDO:0018840,isolated congenital hepatic fibrosis,
+BMGC_DS00542,BMG_DS000689,,Conjunctival Diseases,Conjunctival Diseases,,,,DOID:4251,conjunctival disease,C0009759,D003229,,MONDO:0006170,conjunctival disorder,
+BMGC_DS00543,BMG_DS000690,,,,,,,DOID:5467,conjunctival cancer,C0009761,,,MONDO:0020204,conjunctival tumor,
+BMGC_DS00544,BMG_DS000691,193858003;9826008;193857008,Conjunctivitis,Conjunctivitis,,,H10,DOID:6195,conjunctivitis,C0009763,D003231,MTHU036374,MONDO:0003799,conjunctivitis,Unspecified acute conjunctivitis | Conjunctivitis | Conjunctivitis &/or unspecified acute conjunctivitis | Conjunctivitis &/or unspecified acute conjunctivitis (disorder) | Conjunctivitis | Inflammation of conjunctiva | Conjunctivitis (disorder) | Pink eye disease | Eye infection &/or conjunctivitis (& [acute]) | Eye infection | Acute conjunctivitis | Conjunctivitis | Eye infection &/or conjunctivitis (& [acute]) (disorder)
+BMGC_DS00545,BMG_DS000692,,"Conjunctivitis, Acute Hemorrhagic","Conjunctivitis, Acute Hemorrhagic",,,,DOID:11227,acute hemorrhagic conjunctivitis,C0009765,D003232,,MONDO:0005634,acute hemorrhagic conjunctivitis,
+BMGC_DS00546,BMG_DS000693,,Allergic Conjunctivitis,"Conjunctivitis, Allergic",,,,DOID:11204,allergic conjunctivitis,C0009766,D003233,,MONDO:0005642,atopic conjunctivitis,
+BMGC_DS00547,BMG_DS000694,17482009;193877001;128350005,Bacterial conjunctivitis,,,,,DOID:9700,bacterial conjunctivitis,C0009768,,,MONDO:0006668,bacterial conjunctivitis,Mucopurulent conjunctivitis | Mucopurulent conjunctivitis (disorder) | Bacterial conjunctivitis | Bacterial conjunctivitis (disorder)
+BMGC_DS00548,BMG_DS000695,,"Conjunctivitis, Giant Papillary","Conjunctivitis, Allergic",,,,DOID:2457,giant papillary conjunctivitis,C0009769,D003233,,MONDO:0002308,giant papillary conjunctivitis,
+BMGC_DS00549,BMG_DS000696,266109000;186674002;111840005,Inclusion conjunctivitis,,,,,DOID:13800,inclusion conjunctivitis,C0009770,,,MONDO:0005808,inclusion conjunctivitis,Inclusion conjunctivitis | Paratrachoma | Inclusion conjunctivitis (disorder) | (Conjunctivitis: [inclusion] or [swimming pool]) or (paratrachoma) | Paratrachoma | Inclusion conjunctivitis | Swimming pool conjunctivitis | (Conjunctivitis: [inclusion] or [swimming pool]) or (paratrachoma) (disorder) | Inclusion conjunctivitis | Inclusion conjunctivitis (disorder)
+BMGC_DS00550,BMG_DS000697,,"Conjunctivitis, Vernal","Conjunctivitis, Allergic",,,,DOID:2474,vernal conjunctivitis,C0009773,D003233,,MONDO:0002313,vernal conjunctivitis,
+BMGC_DS00551,BMG_DS000699,,Connective Tissue Diseases,Connective Tissue Diseases,,,,DOID:65,connective tissue disease,C0009782,D003240,,MONDO:0003900,connective tissue disorder,
+BMGC_DS00552,BMG_DS000700,,,,,,,,,C0009806,,,MONDO:0002203,constipation disorder,
+BMGC_DS00553,BMG_DS000701,,,,,,,DOID:1768,conversion disorder,C0009946,,,MONDO:0002104,conversion disorder,
+BMGC_DS00554,BMG_DS000702,,Febrile Convulsions,"Seizures, Febrile",,,,,,C0009952,D003294,,,,
+BMGC_DS00555,BMG_DS000704,,Corneal Diseases,Corneal Diseases,,,,DOID:10124,corneal disease,C0010034,D003316,,MONDO:0000942,corneal disorder,
+BMGC_DS00556,BMG_DS000705,77797009,Hereditary corneal dystrophy,,,,,DOID:2566,corneal dystrophy,C0010035,,,,,Hereditary corneal dystrophy | Hereditary corneal dystrophy (disorder)
+BMGC_DS00557,BMG_DS000706,5587004,Corneal dystrophy,,,,,DOID:2566,corneal dystrophy,C0010036,,MTHU015719,MONDO:0018102,corneal dystrophy,Corneal dystrophy | Corneal dystrophy (disorder)
+BMGC_DS00558,BMG_DS000707,,,,,,,DOID:11030,corneal edema,C0010037,,,MONDO:0006712,corneal edema,
+BMGC_DS00559,BMG_DS000708,,Corneal Ulcer,Corneal Ulcer,,,,DOID:8463,corneal ulcer,C0010043,D003320,,MONDO:0004577,corneal ulcer,
+BMGC_DS00560,BMG_DS000709,,Coronary Aneurysm,Coronary Aneurysm,,,,DOID:3362,coronary aneurysm,C0010051,D003323,,MONDO:0006714,coronary aneurysm,
+BMGC_DS00561,BMG_DS000710,,Coronary Arteriosclerosis,Coronary Artery Disease,,,,DOID:3393,coronary artery disease,C0010054,D003324,,MONDO:0021661,coronary atherosclerosis,
+BMGC_DS00562,BMG_DS000711,41702007;53741008,Coronary heart disease,,,,,DOID:3393,coronary artery disease,C0010068,,,,,Coronary atherosclerosis | Coronary sclerosis | Arteriosclerotic heart disease | ASHD | Atherosclerotic heart disease | Coronary atheroma | Coronary heart disease | Coronary artery disease | CHD - Coronary heart disease | CAD - Coronary artery disease | Ischemic heart disease | Myocardial ischemia | Myocardial ischaemia | Ischaemic heart disease | Cardiac ischaemia | IHD - Ischaemic heart disease | Cardiac ischemia | IHD - Ischemic heart disease | Coronary atherosclerosis (disorder) | Coronary arteriosclerosis | Coronary arteriosclerosis (disorder) | Arteriosclerotic heart disease | CAD - Coronary artery disease | Coronary artery disease | Coronary sclerosis | CHD - Coronary heart disease | Coronary heart disease
+BMGC_DS00563,BMG_DS000712,,Coronary Thrombosis,Coronary Thrombosis,,,,DOID:11847,coronary thrombosis,C0010072,D003328,,MONDO:0006716,coronary thrombosis,
+BMGC_DS00564,BMG_DS000713,,Coronary Artery Vasospasm,Coronary Vasospasm,,,,DOID:11840,coronary artery vasospasm,C0010073,D003329,,MONDO:0005356,coronary vasospasm,
+BMGC_DS00565,BMG_DS000715,,Corpus Luteum Cyst,Ovarian Cysts,,,,,,C0010093,D010048,,MONDO:0001625,corpus luteum cyst,
+BMGC_DS00566,BMG_DS000718,154344005;266193008;70090004,Cowpox,Cowpox,,,B08.010,DOID:8956,cowpox,C0010232,D015605,,MONDO:0005720,cowpox,Cowpox | Milker's node | Smallpox | Orf | Roseola infantum | Variola major | Other viral exanthemata | Fourth disease | Milkers' node | Fifth disease | Parascarlatina | Pseudocowpox | (Viral exanthemata [& variants]) or (orf) or (milkers node) | (Viral exanthemata [& variants]) or (orf) or (milkers node) (disorder) | Pseudocowpox | Fifth disease | Other viral exanthemata | Roseola infantum | Variola major | Cowpox | Parascarlatina | Fourth disease | Milkers' node | Milker's node | Smallpox | Orf | (Viral exanthemata [& variants]) or (orf) or (milkers node) | (Viral exanthemata [& variants]) or (orf) or (milkers node) (disorder) | Cowpox | Cowpox (disorder)
+BMGC_DS00567,BMG_DS000719,,Coxsackievirus Infections,Coxsackievirus Infections,,,,,,C0010246,D003384,,MONDO:0005721,coxsackievirus infectious disease,
+BMGC_DS00568,BMG_DS000721,,,,,,,DOID:5656,cranial nerve disease,C0010266,,,MONDO:0003569,cranial nerve neuropathy,
+BMGC_DS00569,BMG_DS000722,,,,,,,DOID:2815,cranial nerve malignant neoplasm,C0010267,,,MONDO:0002633,cranial nerve neoplasm,
+BMGC_DS00570,BMG_DS000724,,Craniofacial Dysostosis,Craniofacial Dysostosis,,,,DOID:2339,Crouzon syndrome,C0010273,D003394,123500,MONDO:0007405,Crouzon syndrome,
+BMGC_DS00571,BMG_DS000725,,,,,,,DOID:3840,craniopharyngioma,C0010276,,,MONDO:0018907,craniopharyngioma,
+BMGC_DS00572,BMG_DS000726,205414007;205411004;57219006,Craniosynostosis,Craniosynostoses,LB70.0Z,"Craniosynostosis, unspecified",Q75.0,DOID:2340,craniosynostosis,C0010278,D003398,,MONDO:0015469,craniosynostosis,Craniosynostosis | Craniosynostosis (disorder) | (Craniosynostosis) or (scaphocephaly) | Scaphocephaly | Craniosynostosis | (Craniosynostosis) or (scaphocephaly) (disorder) | Craniosynostosis syndrome | Craniostosis | Craniosynostosis | Premature closure of cranial sutures | Congenital ossification of cranial sutures | Congenital ossification of sutures of skull | Craniostenosis | Craniosynostosis syndrome (disorder) | CSO - Craniosynostosis | Premature cranial suture closure
+BMGC_DS00573,BMG_DS000727,,Congenital Hypothyroidism,Congenital Hypothyroidism,,,,DOID:0050328,congenital hypothyroidism,C0010308,D003409,,MONDO:0018612,congenital hypothyroidism,
+BMGC_DS00574,BMG_DS000728,,Cri-du-Chat Syndrome,Cri-du-Chat Syndrome,,,,DOID:12580,Cri-Du-Chat syndrome,C0010314,D003410,123450,MONDO:0007404,Cri-du-chat syndrome,
+BMGC_DS00575,BMG_DS000729,,,,,,,DOID:3803,Crigler-Najjar syndrome,C0010324,,218800,MONDO:0021020,Crigler-Najjar syndrome type 1,
+BMGC_DS00576,BMG_DS000731,,Critical Illness,Critical Illness,,,,,,C0010340,D016638,,,,
+BMGC_DS00577,BMG_DS000732,,Crohn Disease,Crohn Disease,,,,,,C0010346,D003424,,MONDO:0005011,Crohn disease,
+BMGC_DS00578,BMG_DS000734,71186008,Croup,Croup,,,,DOID:9395,croup,C0010380,D003440,,MONDO:0005722,croup,Croup | Croup syndrome | Croup (disorder)
+BMGC_DS00579,BMG_DS000736,,Cruveilhier-Baumgarten Syndrome,"Hypertension, Portal",,,,,,C0010398,D006975,,,,
+BMGC_DS00580,BMG_DS000737,30911005,Cryoglobulinemia,Cryoglobulinemia,4B4Z,"Diseases of the immune system, unspecified",D89.1,DOID:2917,cryoglobulinemia,C0010403,D003449,,MONDO:0005576,cryoglobulinemia,Cryoglobulinemia | Cryoimmunoglobulinemia | Cryoimmunoglobulinaemia | Cryoglobulinaemia | Cryoglobulinemia (disorder)
+BMGC_DS00581,BMG_DS000738,42386007,Infection by Cryptococcus neoformans,,,,,DOID:12053,cryptococcosis,C0010414,,,MONDO:0005724,cryptococcosis,Cryptococcosis | Torula | Torulosis | Infection by Cryptococcus neoformans | European cryptococcosis | European blastomycosis | Busse-Buschke's disease | Busse-Buschke disease | Cryptococcosis (disorder)
+BMGC_DS00582,BMG_DS000739,,,,,,,DOID:11383,cryptorchidism,C0010417,,219050,MONDO:0009047,cryptorchidism,
+BMGC_DS00583,BMG_DS000740,186126003;58777003;240370009,Cryptosporidiosis,Cryptosporidiosis,1A32,Cryptosporidiosis,A07.2,DOID:1733,cryptosporidiosis,C0010418,D003457,,MONDO:0015474,cryptosporidiosis,Cryptosporidiosis | Cryptosporidiosis (disorder) | Infection by Cryptosporidium | Cryptosporidium infection | Infection caused by Cryptosporidium (disorder) | Infection caused by Cryptosporidium | Cryptosporidiasis | Cryptosporidiosis | Cryptosporidiosis (disorder)
+BMGC_DS00584,BMG_DS000741,,Curling Ulcer,Duodenal Ulcer,,,,DOID:1724,duodenal ulcer,C0010474,D004381,,,,
+BMGC_DS00585,BMG_DS000742,,Cushing Syndrome,Cushing Syndrome,,,,DOID:446,primary hyperaldosteronism,C0010481,D003480,,MONDO:0018912,Cushing syndrome,
+BMGC_DS00586,BMG_DS000744,,Cutis Laxa,Cutis Laxa,,,,DOID:3144,cutis laxa,C0010495,D003483,,MONDO:0016175,cutis laxa,
+BMGC_DS00587,BMG_DS000745,267719008;17657000;155116005,Cyclitis,,,,,,,C0010543,,,,,Cyclitis | Ciliary body disorders | Uveitis | Disorders of iris and ciliary body | Iris disorders | Iris/ciliary body disorders | Iris &/or ciliary body disorders (& [cyclitis] or [uveitis]) | Iris &/or ciliary body disorders (& [cyclitis] or [uveitis]) (disorder) | Cyclitis | Cyclitis (disorder) | Cyclitis | Iris/ciliary body disorders | Disorders of iris and ciliary body | Ciliary body disorders | Iris disorders | Uveitis | Iris &/or ciliary body disorders (& [cyclitis] or [uveitis]) | Iris &/or ciliary body disorders (& [cyclitis] or [uveitis]) (disorder)
+BMGC_DS00588,BMG_DS000746,,,,,,,DOID:845,cyclothymic disorder,C0010598,,,MONDO:0004572,cyclothymic disorder,
+BMGC_DS00589,BMG_DS000747,,,,,,,DOID:4866,salivary gland adenoid cystic carcinoma,C0010606,,,MONDO:0004971,adenoid cystic carcinoma,
+BMGC_DS00590,BMG_DS000748,,,,,,,DOID:3111,cystadenocarcinoma,C0010631,,,MONDO:0005596,cystadenocarcinoma,
+BMGC_DS00591,BMG_DS000749,,,,,,,DOID:2634,cystadenoma,C0010633,,,MONDO:0002369,cystadenoma,
+BMGC_DS00592,BMG_DS000754,,Cystic Fibrosis,Cystic Fibrosis,,,,DOID:1485,cystic fibrosis,C0010674,D003550,219700,MONDO:0009061,cystic fibrosis,
+BMGC_DS00593,BMG_DS000755,59051007,Cysticercosis,Cysticercosis,,,B69,DOID:10079,cysticercosis,C0010678,D003551,,MONDO:0015484,cysticercosis,Cysticercosis | Cysticerciasis | Cysticercosis (disorder) | Larval taeniasis | Larval teniasis
+BMGC_DS00594,BMG_DS000756,154738008;267498002;85020001,Cystinuria,Cystinuria,,,E72.01,DOID:9266,cystinuria,C0010691,D003555,220100,MONDO:0009067,cystinuria,Albinism | Cystinuria | Glucose-6-phosphate dehydrogenase deficiency | Glycogen storage disease | Glucose-6-phosph.dehydr.defic. | Von Gierke's disease | von Gierke disease | Other amino-acid/carbohydrate | (Other amino acid/carbohydrate) or (albinism) or (cystinuria) or (glucose-6-phosphate dehydrogenase deficiency) or (galactosemia) or (glycogen storage disease) or (Von Gierke's disease) | (Other amino acid/carbohydrate) or (albinism) or (cystinuria) or (glucose-6-phosphate dehydrogenase deficiency) or (galactosaemia) or (glycogen storage disease) or (Von Gierke's disease) | Galactosaemia | Galactosemia | (Other amino acid/carbohydrate) or (albinism) or (cystinuria) or (glucose-6-phosphate dehydrogenase deficiency) or (galactosaemia) or (glycogen storage disease) or (Von Gierke's disease) (disorder) | Cystinuria | Glucose-6-phosphate dehydrogenase deficiency | Albinism | Other amino-acid/carbohydrate | Glycogen storage disease | von Gierke disease | Von Gierke's disease | Glucose-6-phosph.dehydr.defic. | Galactosaemia | Galactosemia | (Other amino acid/carbohydrate) or (albinism) or (cystinuria) or (glucose-6-phosphate dehydrogenase deficiency) or (galactosaemia) or (glycogen storage disease) or (Von Gierke's disease) | (Other amino acid/carbohydrate) or (albinism) or (cystinuria) or (glucose-6-phosphate dehydrogenase deficiency) or (galactosemia) or (glycogen storage disease) or (Von Gierke's disease) | (Other amino acid/carbohydrate) or (albinism) or (cystinuria) or (glucose-6-phosphate dehydrogenase deficiency) or (galactosaemia) or (glycogen storage disease) or (Von Gierke's disease) (disorder) | Cystinuria | CSNU - Cystinuria | Cystinuria (disorder)
+BMGC_DS00595,BMG_DS000757,38822007,Cystitis,Cystitis,,,N30,DOID:1679,cystitis,C0010692,D003556,,MONDO:0006032,cystitis,Cystitis | Cystitis (disorder) | Bladder infection
+BMGC_DS00596,BMG_DS000759,,,,,,,DOID:1631,benign breast phyllodes tumor,C0010701,,,MONDO:0005078,phyllodes tumor,
+BMGC_DS00597,BMG_DS000760,,Cytomegalovirus Infections,Cytomegalovirus Infections,,,,,,C0010823,D003586,,MONDO:0005132,cytomegalovirus infection,
+BMGC_DS00598,BMG_DS000761,155183008;267738004;85777005,Dacryocystitis,Dacryocystitis,,,,DOID:9938,dacryocystitis,C0010930,D003607,MTHU004835,MONDO:0004926,dacryocystitis,"Dacryocystitis &/or acute/chronic | Dacryocystitis acute/chronic | Dacryocystitis, acute/chronic | Dacryocystitis | Dacryocystitis &/or acute/chronic (disorder) | Dacryocystitis | Dacryocystitis, acute/chronic | Dacryocystitis acute/chronic | Dacryocystitis &/or acute/chronic | Dacryocystitis &/or acute/chronic (disorder) | Dacryocystitis | Dacryocystitis (disorder)"
+BMGC_DS00599,BMG_DS000762,,Dandy-Walker Syndrome,Dandy-Walker Syndrome,,,,DOID:2785,Dandy-Walker syndrome,C0010964,D003616,220200,MONDO:0009072,Dandy-Walker syndrome,
+BMGC_DS00600,BMG_DS000763,,Prelingual Deafness,Deafness,,,,,,C0011052,D003638,,,,
+BMGC_DS00601,BMG_DS000767,,Deficiency Diseases,Deficiency Diseases,,,,DOID:5113,nutritional deficiency disease,C0011156,D003677,,,,
+BMGC_DS00602,BMG_DS000770,,Deglutition Disorders,Deglutition Disorders,,,,,,C0011168,D003680,,,,
+BMGC_DS00603,BMG_DS000771,34095006;154759001,Dehydration,Dehydration,,,E86.0,,,C0011175,D003681,MTHU000177,,,Dehydration | Pure water depletion syndrome | Dehydration (disorder) | Dehydration | Dehydration (disorder)
+BMGC_DS00604,BMG_DS000772,,Dejerine-Sottas Disease,Hereditary Sensory and Motor Neuropathy,,,,,,C0011195,D015417,145900,MONDO:0007790,Charcot-Marie-Tooth disease type 3,
+BMGC_DS00605,BMG_DS000773,,,,,,,,,C0011206,,,MONDO:0045057,delirium,
+BMGC_DS00606,BMG_DS000774,,,,,,,DOID:2047,hepatitis D,C0011226,,,MONDO:0005789,hepatitis D virus infection,
+BMGC_DS00607,BMG_DS000775,,,,,,,DOID:778,delusional disorder,C0011251,,,MONDO:0004359,delusional disorder,
+BMGC_DS00608,BMG_DS000776,56267009,Multi-infarct dementia,,,,,DOID:8725,vascular dementia,C0011263,,,MONDO:0043224,multi-infarct dementia,Multi-infarct dementia | Arteriosclerotic dementia | Multi-infarct dementia (disorder) | Multi infarct dementia | MID - multi-infarct dementia
+BMGC_DS00609,BMG_DS000777,,"Dementia, Vascular","Dementia, Vascular",,,,DOID:8725,vascular dementia,C0011269,D015140,,MONDO:0004648,vascular dementia,
+BMGC_DS00610,BMG_DS000779,,Demyelinating Diseases,Demyelinating Diseases,,,,DOID:3213,demyelinating disease,C0011303,D003711,,MONDO:0002562,demyelinating disease,
+BMGC_DS00611,BMG_DS000780,,Dengue Fever,Dengue,,,,DOID:12205,dengue disease,C0011311,D003715,,MONDO:0005502,dengue disease,
+BMGC_DS00612,BMG_DS000781,155632007;80967001,Dental caries,,,,K02,DOID:216,dental caries,C0011334,,MTHU004627,MONDO:0005276,dental caries,Dental caries | Dental caries (disorder) | Dental caries | Tooth caries | Dental cavity | Tooth decay | Tooth decayed | Dental decay | Teeth decayed | Dental caries (disorder) | Carious lesion
+BMGC_DS00613,BMG_DS000783,,Dental Enamel Hypoplasia,Dental Enamel Hypoplasia,,,,DOID:693,dental enamel hypoplasia,C0011351,D003744,,MONDO:0004038,dental enamel hypoplasia,
+BMGC_DS00614,BMG_DS000784,,Dental Plaque,Dental Plaque,,,,,,C0011389,D003773,,,,
+BMGC_DS00615,BMG_DS000786,,Dental Pulp Calcification,Dental Pulp Calcification,,,,DOID:5608,dental pulp calcification,C0011401,D003784,,MONDO:0003542,dental pulp calcification,
+BMGC_DS00616,BMG_DS000787,,Dental Pulp Diseases,Dental Pulp Diseases,,,,DOID:5330,dental pulp disease,C0011405,D003788,,MONDO:0003394,dental pulp disorder,
+BMGC_DS00617,BMG_DS000789,,Dental Pulp Necrosis,Dental Pulp Necrosis,,,,DOID:11623,dental pulp necrosis,C0011407,D003790,,MONDO:0001326,dental pulp necrosis,
+BMGC_DS00618,BMG_DS000791,,Dentin Dysplasia,Dentin Dysplasia,,,,DOID:701,dentin dysplasia,C0011430,D003805,,MONDO:0015613,dentin dysplasia,
+BMGC_DS00619,BMG_DS000792,,Dentin Sensitivity,Dentin Sensitivity,,,,DOID:698,dentin sensitivity,C0011432,D003807,,MONDO:0004059,dentin sensitivity,
+BMGC_DS00620,BMG_DS000794,,,,,,,DOID:4154,dentinogenesis imperfecta,C0011436,,,MONDO:0018849,dentinogenesis imperfecta,
+BMGC_DS00621,BMG_DS000795,,,,,,,DOID:10931,dependent personality disorder,C0011548,,,MONDO:0001157,dependent personality disorder,
+BMGC_DS00622,BMG_DS000796,,,,,,,DOID:1596,depressive disorder,C0011570,,,,,
+BMGC_DS00623,BMG_DS000797,,,,,,,DOID:1595,melancholic depression,C0011573,,,MONDO:0012048,endogenous depression,
+BMGC_DS00624,BMG_DS000798,,,,,,,DOID:4964,neurotic disorder,C0011579,,,,,
+BMGC_DS00625,BMG_DS000799,,,,,,,,,C0011581,,,MONDO:0002050,depressive disorder,
+BMGC_DS00626,BMG_DS000800,703938007;182782007;4979002;238538009;43116000,Dermatitis,Dermatitis,,,,DOID:2723,dermatitis,C0011603,D003872,MTHU001691,,,Inflammatory dermatosis (disorder) | Inflammatory dermatosis | Dermatitis | Dermatitis | Inflammation of skin | Dermatitis (disorder) | Dermatitis | Dermatitis (disorder) | Eczema | Dermatitis | Eczema (disorder) | Eczema | Eczema (disorder)
+BMGC_DS00627,BMG_DS000801,123702007;399992009;55012006,Exfoliative dermatitis,,,,L26,,,C0011606,,MTHU072636,MONDO:0043233,exfoliative dermatitis,Scaling eczema | Scaling eczematous dermatitis | Exfoliative eczematous dermatitis | Exfoliative eczema | Desquamative eczematous dermatitis | Desquamative eczema | Scaling eczema (disorder) | Exfoliative dermatitis | Erythroderma (disorder) | Erythroderma | Exfoliative dermatitis | Erythrodermatitis | Generalized exfoliative dermatitis | Generalised exfoliative dermatitis | Acute eczema | Erythematous eczema | Erythrodermic eczema | Exfoliative dermatitis | Acute eczema (disorder)
+BMGC_DS00628,BMG_DS000802,,Dermatitis Herpetiformis,Dermatitis Herpetiformis,,,,DOID:8505,dermatitis herpetiformis,C0011608,D003874,,MONDO:0015614,dermatitis herpetiformis,
+BMGC_DS00629,BMG_DS000803,,"Dermatitis, Atopic","Dermatitis, Atopic",,,,DOID:3310,atopic dermatitis,C0011615,D003876,603165,MONDO:0004980,atopic eczema,
+BMGC_DS00630,BMG_DS000804,,Contact Dermatitis,"Dermatitis, Contact",,,,DOID:2773,contact dermatitis,C0011616,D003877,,MONDO:0005480,contact dermatitis,
+BMGC_DS00631,BMG_DS000806,,Dermatomycoses,Dermatomycoses,,,,DOID:1563,dermatomycosis,C0011630,D003881,,MONDO:0002040,dermatomycosis,
+BMGC_DS00632,BMG_DS000807,38826005;156456005;396230008;201445002,Dermatomyositis,Dermatomyositis,,,,DOID:10223,dermatomyositis,C0011633,D003882,MTHU018873,MONDO:0016367,dermatomyositis,Dermatomyositis | Polymyositis with skin involvement | Adult type dermatomyositis | Wagner-Unverricht syndrome | Dermatomyositis (disorder) | DM - Dermatomyositis | Dermatomyositis | Dermatomyositis (disorder) | Dermatomyositis (disorder) | Dermatomyositis | Wagner-Unverricht syndrome | Polymyositis with skin involvement | DM - Dermatomyositis | Poikilodermatomyositis | Dermatomyositis | Dermatomyositis (& [Poikilodermatomyositis]) | Dermatomyositis (& [Poikilodermatomyositis]) (disorder)
+BMGC_DS00633,BMG_DS000808,47382004;266214005;154394006,Dermatophytosis,,,,B35,DOID:8913,dermatophytosis,C0011636,,,MONDO:0004678,dermatophytosis,Dermatophytosis | Tinea | Ringworm | Microsporic tinea | Dermatophytosis (disorder) | Ringworm | Mycoses | Dermatophytosis-tinea/ringworm | Tinea | Fungal infection | Dermatophytosis | Fungal infections | (Dermatophytosis &/or tinea &/or ringworm) or (fungal infections) or (mycoses) | (Dermatophytosis &/or tinea &/or ringworm) or (fungal infections) or (mycoses) (disorder) | (Dermatophytosis &/or tinea &/or ringworm) or (fungal infections) or (mycoses) | Fungal infection | Dermatophytosis | Tinea | Fungal infections | Mycoses | Ringworm | Dermatophytosis-tinea/ringworm | (Dermatophytosis &/or tinea &/or ringworm) or (fungal infections) or (mycoses) (disorder)
+BMGC_DS00634,BMG_DS000809,186989008;266150008;59089002,Dermatophytosis of groin and perianal area,,,,,DOID:11917,tinea cruris,C0011638,,,MONDO:0001405,dermatophytosis of groin and perianal area,Dhobie itch | Dermatophytosis of groin and perianal area | Tinea cruris | (Dermatophytosis of groin & perianal area) or (Dhobie itch) or (tinea cruris) | (Dermatophytosis of groin & perianal area) or (Dhobie itch) or (tinea cruris) (disorder) | Dermatophytosis of groin and perianal area | Dermatophytosis of groin and perianal area (disorder) | Tinea cruris | Tinea inguinalis | Eczema marginatum | Tinea of groin | Tinea of perianal region | Dhobie itch | Jock itch | Ringworm of genitocrural region | Tinea cruris (disorder) | Dermatophytosis of groin | Dermatophytosis of groin and pubic area | Hebrae | Dermatophytosis of groin and perianal area
+BMGC_DS00635,BMG_DS000810,,,,,,,DOID:4337,tinea capitis,C0011640,,,MONDO:0002967,dermatophytosis of scalp or beard,
+BMGC_DS00636,BMG_DS000811,201440007;201441006;89155008;267874003;128457007;268049000;156451000,Scleroderma,,,,,DOID:419,scleroderma,C0011644,,MTHU010137,MONDO:0019340,scleroderma,Scleroderma (& [acrosclerosis] or [systemic sclerosis]) | Acrosclerosis | Systemic sclerosis | Scleroderma | Scleroderma (& [acrosclerosis] or [systemic sclerosis]) (disorder) | Scleroderma | Scleroderma (disorder) | Systemic sclerosis | Systemic scleroderma | Thibierge-Weissenbach syndrome | SS - Systemic sclerosis | Systemic sclerosis (disorder) | Scleroderma syndrome | Scleroderma syndrome (disorder) | Scleroderma (& [systemic sclerosis]) | Scleroderma | Systemic sclerosis | Scleroderma (& [systemic sclerosis]) (disorder)
+BMGC_DS00637,BMG_DS000812,,Dermatosis Papulosa Nigra,,,,,DOID:4400,dermatosis papulosa nigra,C0011645,C562379,125600,MONDO:0007446,dermatosis papulosa nigra,
+BMGC_DS00638,BMG_DS000813,,,,,,,DOID:2658,dermoid cyst,C0011649,,,MONDO:0002378,dermoid cyst,
+BMGC_DS00639,BMG_DS000814,,,,,,,DOID:9923,developmental coordination disorder,C0011757,,,MONDO:0004922,developmental coordination disorder,
+BMGC_DS00640,BMG_DS000815,,,,,,,DOID:9565,dextrocardia,C0011813,,,MONDO:0015661,dextrocardia,
+BMGC_DS00641,BMG_DS000816,,Diabetes,,,,,,,C0011847,,MTHU050182,,,
+BMGC_DS00642,BMG_DS000817,,Diabetes Insipidus,Diabetes Insipidus,,,,DOID:9409,diabetes insipidus,C0011848,D003919,,MONDO:0004782,diabetes insipidus,
+BMGC_DS00643,BMG_DS000818,,Diabetes Mellitus,Diabetes Mellitus,,,,DOID:9351,diabetes mellitus,C0011849,D003920,,MONDO:0005015,diabetes mellitus,
+BMGC_DS00644,BMG_DS000819,,"Diabetes Mellitus, Insulin-Dependent","Diabetes Mellitus, Type 1",,,,DOID:9744,type 1 diabetes mellitus,C0011854,D003922,222100,MONDO:0005147,type 1 diabetes mellitus,
+BMGC_DS00645,BMG_DS000820,,Lipoatrophic Diabetes Mellitus,"Diabetes Mellitus, Lipoatrophic",,,,DOID:11712,lipoatrophic diabetes mellitus,C0011859,D003923,,MONDO:0005827,lipoatrophic diabetes,
+BMGC_DS00646,BMG_DS000821,,"Diabetes Mellitus, Non-Insulin-Dependent","Diabetes Mellitus, Type 2",,,,DOID:9352,type 2 diabetes mellitus,C0011860,D003924,125853,MONDO:0005148,type 2 diabetes mellitus,
+BMGC_DS00647,BMG_DS000823,982001;127014009,Diabetic peripheral angiopathy,,,,,DOID:11713,diabetic angiopathy,C0011871,,,MONDO:0000960,diabetic peripheral angiopathy,Diabetes with peripheral circulatory disorders | Diabetes with peripheral circulatory disorders (disorder) | Diabetic peripheral angiopathy | Diabetic peripheral vascular disease | Diabetes with peripheral circulatory disorder | Peripheral angiopathy due to diabetes mellitus | Peripheral angiopathy due to diabetes mellitus (disorder)
+BMGC_DS00648,BMG_DS000824,,Diabetic Angiopathies,Diabetic Angiopathies,,,,DOID:11713,diabetic angiopathy,C0011875,D003925,,,,
+BMGC_DS00649,BMG_DS000825,43959009,Cataract due to diabetes mellitus,,,,,DOID:13328,diabetic cataract,C0011876,,,MONDO:0001687,diabetic cataract,Diabetic cataract | Cataract due to diabetes mellitus | Cataract of eye due to diabetes mellitus (disorder) | Cataract of eye due to diabetes mellitus
+BMGC_DS00650,BMG_DS000827,,Diabetic Ketoacidosis,Diabetic Ketoacidosis,,,,DOID:1837,diabetic ketoacidosis,C0011880,D016883,,MONDO:0012819,diabetic ketoacidosis,
+BMGC_DS00651,BMG_DS000828,,Diabetic Nephropathy,Diabetic Nephropathies,,,,,,C0011881,D003928,,MONDO:0005016,diabetic kidney disease,
+BMGC_DS00652,BMG_DS000829,,Diabetic Neuropathies,Diabetic Neuropathies,,,,DOID:9743,diabetic neuropathy,C0011882,D003929,,MONDO:0006626,diabetic neuropathy,
+BMGC_DS00653,BMG_DS000830,,Diabetic Retinopathy,Diabetic Retinopathy,,,,DOID:8947,diabetic retinopathy,C0011884,D003930,,MONDO:0005266,diabetic retinopathy,
+BMGC_DS00654,BMG_DS000831,,Diaper Rash,Diaper Rash,,,,,,C0011974,D003963,,,,
+BMGC_DS00655,BMG_DS000832,,,,,,,DOID:10480,diaphragmatic eventration,C0011981,,,MONDO:0006726,diaphragmatic eventration,
+BMGC_DS00656,BMG_DS000834,,Camurati-Engelmann Syndrome,Camurati-Engelmann Syndrome,,,,DOID:4997,Camurati-Engelmann disease,C0011989,D003966,131300,MONDO:0007542,Camurati-Engelmann disease,
+BMGC_DS00657,BMG_DS000836,,,,,,,DOID:5574,VIPoma,C0011993,,,MONDO:0019960,VIPoma,
+BMGC_DS00658,BMG_DS000837,,,,,,,,,C0011999,,222500,MONDO:0009106,diastematomyelia,
+BMGC_DS00659,BMG_DS000838,8410006,Dicrocoeliasis,Dicrocoeliasis,,,,DOID:1219,dicrocoeliasis,C0012102,D004011,,MONDO:0005729,dicrocoeliasis,Dicrocoeliasis | Dicrocoeliosis | Dicroceliasis | Lancet fluke infection | Dicroceliosis | Dicrocoeliasis (disorder) | Infection caused by Dicrocoelium dendriticum
+BMGC_DS00660,BMG_DS000840,,Dientamoebiasis,Dientamoebiasis,,,,DOID:946,dientamoebiasis,C0012147,D004030,,MONDO:0024608,dientamoebiasis,
+BMGC_DS00661,BMG_DS000841,,DiGeorge Syndrome,DiGeorge Syndrome,,,,DOID:11198,DiGeorge syndrome,C0012236,D004062,188400,MONDO:0008564,DiGeorge syndrome,
+BMGC_DS00662,BMG_DS000842,,Digestive System Disorders,Digestive System Diseases,,,,DOID:77,gastrointestinal system disease,C0012242,D004066,,,,
+BMGC_DS00663,BMG_DS000843,,,,,,,DOID:3119,gastrointestinal system cancer,C0012243,,,MONDO:0021223,digestive system neoplasm,
+BMGC_DS00664,BMG_DS000845,,Dipetalonema Infections,Dipetalonema Infections,,,,DOID:14422,dipetalonemiasis,C0012517,D004154,,MONDO:0005731,dipetalonemiasis,
+BMGC_DS00665,BMG_DS000846,154299004;3739008;397428000,Diphtheria,,,,A36,,,C0012546,,,MONDO:0005504,diphtheria,Diphtheria | Diphtheria (disorder) | Diphtheria | Infection due to Corynebacterium diphtheriae | Diphtheria (disorder) | Diphtheria (disorder) | Diphtheria
+BMGC_DS00666,BMG_DS000849,18901009,Cutaneous diphtheria,,1C17.3,Cutaneous diphtheria,A36.3,DOID:12275,cutaneous diphtheria,C0012555,,,MONDO:0001479,cutaneous diphtheria,Cutaneous diphtheria | Cutaneous diphtheria (disorder)
+BMGC_DS00667,BMG_DS000853,187151009;49047003,Diphyllobothriasis,Diphyllobothriasis,1F71,Diphyllobothriasis,B70.0,DOID:10075,diphyllobothriasis,C0012561,D004169,,MONDO:0015260,diphyllobothriasis,Fish tapeworm infection | Diphyllobothrium infection | Diphyllobothriasis | Diphyllobothriasis (disorder) | Infection by Diphyllobothrium | Infection by Diphyllobothrium (disorder)
+BMGC_DS00668,BMG_DS000854,139545001;24982008;162276002;155141003,Diplopia,Diplopia,9D46,Impairment of binocular functions,H53.2,,,C0012569,D004172,MTHU000786,,,Diplopia | Diplopia (finding) | Diplopia | Double vision | Diplopia (disorder) | Seeing double | Diplopia | Diplopia (disorder)
+BMGC_DS00669,BMG_DS000855,73328005,Dirofilariasis,Dirofilariasis,1F66.Z,"Filariasis, unspecified",B74.8,DOID:1082,dirofilariasis,C0012602,D004184,,MONDO:0015636,dirofilariasis,Infection by Dirofilaria | Dirofilariasis | Dirofilariosis | Infection caused by Dirofilaria | Infection caused by Dirofilaria (disorder)
+BMGC_DS00670,BMG_DS000856,2304001,Discitis,Discitis,,,,DOID:10986,discitis,C0012624,D015299,,MONDO:0006728,obsolete discitis,Discitis | Discitis (disorder) | Intervertebral discitis | Inflammatory discitis
+BMGC_DS00671,BMG_DS000857,,Discrete Subaortic Stenosis,Discrete Subaortic Stenosis,,,,DOID:5804,discrete subaortic stenosis,C0012628,D021922,,MONDO:0006729,discrete subaortic stenosis,
+BMGC_DS00672,BMG_DS000858,64572001,Disease,Disease,,,,DOID:4,disease,C0012634,D004194,,MONDO:0000001,disease,Disease | Clinical disease AND/OR syndrome | Disorder | Syndrome | Disorders | Diseases | Disease (disorder)
+BMGC_DS00673,BMG_DS000863,,Iron Metabolism Disorders,Iron Metabolism Disorders,,,,DOID:2351,iron metabolism disease,C0012715,D019189,,MONDO:0002279,iron metabolism disease,
+BMGC_DS00674,BMG_DS000864,60853003,Disorder of magnesium metabolism,,,,,,,C0012716,,,,,Disorder of magnesium metabolism | Disorder of magnesium metabolism (disorder)
+BMGC_DS00675,BMG_DS000865,,,,,,,,,C0012734,,,MONDO:0800106,disruptive behavior disorder,
+BMGC_DS00676,BMG_DS000866,308546005;155420000;67076004,Dissecting aortic aneurysm,,,,,,,C0012736,,,,,Dissection of aorta | Dissection of aorta (disorder) | Dissecting aortic aneurysm | Dissecting aortic aneurysm (disorder)
+BMGC_DS00677,BMG_DS000868,,Disseminated Intravascular Coagulation,Disseminated Intravascular Coagulation,,,,DOID:11247,disseminated intravascular coagulation,C0012739,D004211,,MONDO:0001243,disseminated intravascular coagulation,
+BMGC_DS00678,BMG_DS000869,,,,,,,DOID:10935,dissociative disorder,C0012746,,,MONDO:0001160,dissociative disorder,
+BMGC_DS00679,BMG_DS000872,155779000;197095003;18126004;307496006,Diverticulitis,Diverticulitis,,,,DOID:7475,diverticulitis,C0012813,D004238,MTHU026283,MONDO:0004235,diverticulitis,Diverticulitis | Diverticulitis (disorder) | Diverticulitis (& [of intestine]) | Diverticulitis | Diverticulitis (& [of intestine]) (disorder) | Diverticulitis | Diverticulitis (morphologic abnormality)
+BMGC_DS00680,BMG_DS000873,,Colonic Diverticulitis,"Diverticulitis, Colonic",,,,DOID:13254,diverticulitis of colon,C0012814,D004239,,MONDO:0001674,diverticulitis of colon,
+BMGC_DS00681,BMG_DS000875,68047000;398050005,Diverticular disease of colon,,,,,,,C0012819,,,,,Diverticulosis of colon without diverticulitis | Diverticular disease of colon | Diverticulosis of colon | Diverticulosis of the colon | Diverticular disease | Diverticular disease of large intestine | DD - Diverticular disease | Diverticulosis | Diverticulosis of colon without diverticulitis (disorder) | Diverticular disease of colon (disorder) | Diverticular disease of colon | Symptomatic diverticulosis of colon
+BMGC_DS00682,BMG_DS000877,,Dog Diseases,Dog Diseases,,,,,,C0012979,D004283,,MONDO:0024919,dog disease,
+BMGC_DS00683,BMG_DS000878,,,,,,,DOID:6406,double outlet right ventricle,C0013069,,,MONDO:0018089,double outlet right ventricle,
+BMGC_DS00684,BMG_DS000880,,Down Syndrome,Down Syndrome,,,,DOID:14250,Down syndrome,C0013080,D004314,190685,MONDO:0008608,Down syndrome,
+BMGC_DS00685,BMG_DS000881,396334002;48874008,Dracunculiasis,Dracunculiasis,,,B72,DOID:14418,dracunculiasis,C0013100,D004320,,MONDO:0016472,dracunculiasis,Infection by Dracunculus medinensis | Dracontiasis - guinea-worm | Dracontiasis | Dracunculosis | Guinea-worm infection | Guinea worm disease | Dracunculiasis | Infection caused by Dracunculus medinensis | Infection caused by Dracunculus medinensis (disorder) | Infection by Dracunculus medinensis | Dracontiasis | Dracunculiasis | Guinea worm disease | Dracunculosis | Guinea-worm ulcer | Guinea-worm infection | Dracontiasis - guinea-worm | Infection by Dracunculus medinensis (disorder)
+BMGC_DS00686,BMG_DS000882,,,,,,,DOID:302,substance abuse,C0013146,,,,,
+BMGC_DS00687,BMG_DS000883,,,,,,,,,C0013182,,,MONDO:0000775,drug allergy,
+BMGC_DS00688,BMG_DS000884,,Dry Eye Syndromes,Dry Eye Syndromes,,,,DOID:10140,dry eye syndrome,C0013238,D015352,,MONDO:0006733,dry eye syndrome,
+BMGC_DS00689,BMG_DS000885,12033006;251331003,Alveolar periostitis,,,,,DOID:13585,alveolar periostitis,C0013240,,,MONDO:0001752,alveolar periostitis,Marginal periodontitis | Marginal periodontitis (disorder) | Alveolar periostitis | Alveolar periostitis (disorder)
+BMGC_DS00690,BMG_DS000886,,Duane Retraction Syndrome,Duane Retraction Syndrome,,,,DOID:12557,Duane retraction syndrome,C0013261,D004370,,MONDO:0007473,Duane retraction syndrome,
+BMGC_DS00691,BMG_DS000887,,"Muscular Dystrophy, Duchenne","Muscular Dystrophy, Duchenne",,,,DOID:11723,Duchenne muscular dystrophy,C0013264,D020388,310200,MONDO:0010679,Duchenne muscular dystrophy,
+BMGC_DS00692,BMG_DS000888,,,,,,,DOID:13832,patent ductus arteriosus,C0013274,,,MONDO:0011827,patent ductus arteriosus,
+BMGC_DS00693,BMG_DS000889,,Dumping Syndrome,Dumping Syndrome,,,,DOID:14495,dumping syndrome,C0013288,D004377,,MONDO:0001979,dumping syndrome,
+BMGC_DS00694,BMG_DS000890,,Duodenal Diseases,Duodenal Diseases,,,,DOID:4072,duodenum disease,C0013289,D004378,,MONDO:0002866,duodenal disorder,
+BMGC_DS00695,BMG_DS000891,,,,,,,DOID:1737,duodenal benign neoplasm,C0013291,,,MONDO:0021375,tumor of duodenum,
+BMGC_DS00696,BMG_DS000892,,Duodenal Obstruction,Duodenal Obstruction,,,,DOID:3558,duodenal obstruction,C0013292,D004380,,MONDO:0002688,duodenal obstruction,
+BMGC_DS00697,BMG_DS000893,,Duodenal Ulcer,Duodenal Ulcer,,,,DOID:1724,duodenal ulcer,C0013295,D004381,,MONDO:0005412,duodenal ulcer,
+BMGC_DS00698,BMG_DS000894,155715004;72007001,Duodenitis,Duodenitis,DA51.Z,"Duodenitis, unspecified",K29.8,DOID:8643,duodenitis,C0013298,D004382,MTHU072206,MONDO:0004627,duodenitis,Duodenitis | Duodenitis (disorder)
+BMGC_DS00699,BMG_DS000895,,Duodenogastric Reflux,Duodenogastric Reflux,,,,DOID:4071,duodenogastric reflux,C0013299,D004383,,MONDO:0006735,duodenogastric reflux,
+BMGC_DS00700,BMG_DS000896,,Dupuytren Contracture,Dupuytren Contracture,,,,,,C0013312,D004387,126900,MONDO:0007476,familial Dupuytren contracture,
+BMGC_DS00701,BMG_DS000897,237836003;90482002;205467007;185797004,Dwarfism,Dwarfism,,,,,,C0013336,D004392,MTHU009274,,,Small stature | Short stature disorder | Short stature disorder (disorder) | SS - Short stature | Short stature | Dwarfism | Dwarfism (disorder) | (Achondroplasia) or (achondrogenesis) or (dwarfism (& achondroplastic)) | Achondrogenesis | Dwarfism | Achondroplastic dwarf | Achondroplasia | (Achondroplasia) or (achondrogenesis) or (dwarfism (& achondroplastic)) (disorder) | True dwarfism | Primordial dwarf | Nanosomia | Normal dwarf | Dwarfism (disorder) | Dwarfism
+BMGC_DS00702,BMG_DS000898,367460001;270485009;45617007;190476004;154701008,Pituitary dwarfism,,,,,DOID:0060870,isolated growth hormone deficiency,C0013338,,,MONDO:0006909,pituitary dwarfism,Pituitary dwarfism | Hypopituitary dwarfism | Pituitary nanism | Hyposomatotropic dwarfism | Prepubertal dwarfism | Isolated deficiency of growth hormone in children | Prepuberal dwarfism | Pituitary dwarfism (disorder) | Lorain - Levi dwarfism | Pituitary dwarfism | Pituitary dwarfism (disorder) | Dwarfism: [pituitary] or [hypophyseal (& Lorain-Levi)] | Lorain - Levi dwarfism | Hypophyseal dwarfism | Pituitary dwarfism | Dwarfism: [pituitary] or [hypophyseal (& Lorain-Levi)] (disorder)
+BMGC_DS00703,BMG_DS000899,15241006,Dysautonomia,,,,,,,C0013363,,MTHU005895,MONDO:0044872,dysautonomia,Disorder of autonomic nervous system | Disorder of vegetative system | Dysautonomia | Disorders of autonomic nervous system | Disorder of autonomic nervous system (disorder)
+BMGC_DS00704,BMG_DS000900,,"Dysautonomia, Familial","Dysautonomia, Familial",,,,DOID:11589,Riley-Day syndrome,C0013364,D004402,223900,MONDO:0009131,Riley-Day syndrome,
+BMGC_DS00705,BMG_DS000901,266173000;154268000;111939009,Dysentery,Dysentery,,,,DOID:12384;DOID:13250,dysentery | diarrhea,C0013369,D004403,,MONDO:0001517,dysentery,Specific GIT infectious dis. | Specific gastrointestinal infectious disease | Dysentery | Bacterial gastroenteritis | Gastroenteritis - bact. | Diarrhoea-bact.GIT inf. | (Specific GIT infectious disease) or (dysentery) or (bacterial: [gastroenteritis] or [diarrhoea]) | Diarrhea-bact.GIT inf. | (Specific GIT infectious disease) or (dysentery) or (bacterial: [gastroenteritis] or [diarrhea]) | (Specific GIT infectious disease) or (dysentery) or (bacterial: [gastroenteritis] or [diarrhoea]) (disorder) | (Specific GIT infectious disease) or (dysentery) or (bacterial: [gastroenteritis] or [diarrhea]) | Gastroenteritis - bact. | Specific GIT infectious dis. | Specific gastrointestinal infectious disease | Dysentery | Bacterial gastroenteritis | (Specific GIT infectious disease) or (dysentery) or (bacterial: [gastroenteritis] or [diarrhoea]) | Diarrhea-bact.GIT inf. | Diarrhoea-bact.GIT inf. | (Specific GIT infectious disease) or (dysentery) or (bacterial: [gastroenteritis] or [diarrhoea]) (disorder) | Dysentery | Dysentery (disorder)
+BMGC_DS00706,BMG_DS000902,235747003,Amebic colitis,,,,,,,C0013370,,,MONDO:0024275,amebic dysentery,Amebic colitis | Amoebic colitis | Amebic colitis (disorder)
+BMGC_DS00707,BMG_DS000903,,Shigella Infections,"Dysentery, Bacillary",,,,DOID:12385,shigellosis,C0013371,D004405,,MONDO:0019345,shigellosis,
+BMGC_DS00708,BMG_DS000904,123782009;127389001,Dysgammaglobulinemia,Dysgammaglobulinemia,,,,DOID:11702,dysgammaglobulinemia,C0013374,D004406,MTHU007448,MONDO:0001342,dysgammaglobulinemia,Dysgammaglobulinemia | Dysgammaglobulinaemia | Dysgammaglobulinemia (disorder) | Dysgammaglobulinemia | Dysgammaglobulinaemia | Dysgammaglobulinemia (finding)
+BMGC_DS00709,BMG_DS000905,,,,,,,DOID:4441,dysgerminoma,C0013377,,,MONDO:0003002,dysgerminoma,
+BMGC_DS00710,BMG_DS000906,,"Dyskinesia, Drug-Induced","Dyskinesia, Drug-Induced",,,,,,C0013386,D004409,,MONDO:0006732,drug-induced dyskinesia,
+BMGC_DS00711,BMG_DS000907,,,,,,,DOID:13417,alexia,C0013388,,,,,
+BMGC_DS00712,BMG_DS000908,367433008;29837005;266599000;156030009;198404001,Dysmenorrhea,Dysmenorrhea,,,,,,C0013390,D004412,,,,Menorrhalgia | Dysmenorrhea (finding) | Dysmenorrhoea | Dysmenorrhea | Dysmenorrhea | Dysmenorrhoea | Dysmenorrhea (finding) | Period pain | Menstrual cramps | Dysmenorrhea | Dysmenorrhoea | Dysmenorrhea (disorder) | Menorrhalgia | Dysmenorrhoea | Dysmenorrhea | Dysmenorrhoea (disorder) | Painful menstruation | Period pains | Dysmenorrhea (& spasmodic) | Dysmenorrhea | Painful menorrhea | Spasmodic dysmenorrhea | Painful menorrhoea | Spasmodic dysmenorrhoea | Dysmenorrhoea | Dysmenorrhoea (& spasmodic) | Dysmenorrhoea (& spasmodic) (disorder)
+BMGC_DS00713,BMG_DS000909,,Dysostoses,Dysostoses,,,,DOID:1934,dysostosis,C0013393,D004413,,MONDO:0018234,dysostosis,
+BMGC_DS00714,BMG_DS000911,,,,,,,,,C0013395,,,MONDO:0002268,dyspepsia,
+BMGC_DS00715,BMG_DS000912,,,,,,,DOID:1159,functional gastric disease,C0013396,,,,,
+BMGC_DS00716,BMG_DS000914,,,,,,,DOID:12139,dysthymic disorder,C0013415,,,MONDO:0001442,dysthymic disorder,
+BMGC_DS00717,BMG_DS000916,,,,,,,DOID:543,dystonia,C0013421,,,MONDO:0003441,dystonic disorder,
+BMGC_DS00718,BMG_DS000917,,Dystonia Musculorum Deformans,Dystonia Musculorum Deformans,,,,DOID:0050835,generalized dystonia,C0013423,D004422,,MONDO:0044843,torsion dystonia,
+BMGC_DS00719,BMG_DS000918,51689003;198378001,Dystrophy of vulva,,EB60.0,Lichen sclerosus of vulva,N90.4,DOID:14292,vulvar dystrophy,C0013426,,,MONDO:0001938,vulvar dystrophy,Dystrophy of vulva | Dystrophy of vulva (disorder)
+BMGC_DS00720,BMG_DS000919,,Ear Diseases,Ear Diseases,,,,DOID:2742,auditory system disease,C0013447,D004427,,MONDO:0021205,disorder of ear,
+BMGC_DS00721,BMG_DS000920,,,,,,,DOID:833,auditory system cancer,C0013449,,,MONDO:0021233,ear neoplasm,
+BMGC_DS00722,BMG_DS000922,,,,,,,DOID:8670,eating disorder,C0013473,,,MONDO:0005451,eating disorder,
+BMGC_DS00723,BMG_DS000923,,,,,,,DOID:14289,Ebstein anomaly,C0013481,,224700,MONDO:0009144,Ebstein anomaly,
+BMGC_DS00724,BMG_DS000924,154414008;74942003,Echinococcosis,Echinococcosis,,,B67,DOID:1496,echinococcosis,C0013502,D004443,,MONDO:0005738,echinococcosis,Echinococcosis | Echinococcosis (disorder) | Echinococciasis | Echinococcosis | Hydatid disease | Hydatidosis | Echinococcus disease | Echinococcosis (disorder)
+BMGC_DS00725,BMG_DS000927,36607007,Echinostomiasis,Echinostomiasis,1F8Z,"Diseases due to trematodes, unspecified",B66.8,DOID:1218,echinostomiasis,C0013514,D004451,,MONDO:0005739,echinostomiasis,Echinostomiasis | Echinostomosis | Echinostomiasis (disorder)
+BMGC_DS00726,BMG_DS000928,,,,,,,DOID:4188,echolalia,C0013528,,,MONDO:0002904,echolalia,
+BMGC_DS00727,BMG_DS000930,15938005;156111007;198988006,Eclampsia,Eclampsia,,,O15,DOID:13593,eclampsia,C0013537,D004461,MTHU074894,MONDO:0001754,eclampsia,Eclampsia | Toxemia with convulsions | Eclamptic toxemia | Eclamptic toxaemia | Toxaemia with convulsions | Eclampsia (disorder) | Eclampsia | Eclampsia (disorder)
+BMGC_DS00728,BMG_DS000931,762694009;85791004,Ecthyma,Ecthyma,,,,DOID:11907,ecthyma,C0013568,D004473,,MONDO:0001404,ecthyma,Ecthyma | Ecthyma (disorder)
+BMGC_DS00729,BMG_DS000932,,"Ecthyma, Contagious","Ecthyma, Contagious",,,,DOID:8771,contagious pustular dermatitis,C0013570,D004474,,MONDO:0005717,contagious pustular dermatitis,
+BMGC_DS00730,BMG_DS000933,,Ectodermal Dysplasia,Ectodermal Dysplasia,,,,DOID:2121,ectodermal dysplasia,C0013575,D004476,,MONDO:0019287,ectodermal dysplasia syndrome,
+BMGC_DS00731,BMG_DS000934,,Ectoparasitic Infestations,Ectoparasitic Infestations,,,,DOID:4110,parasitic ectoparasitic infectious disease,C0013578,D004478,,MONDO:0002875,parasitic ectoparasitic infectious disease,
+BMGC_DS00732,BMG_DS000936,,,,,,,DOID:0111148,isolated ectopia lentis,C0013581,,,,,
+BMGC_DS00733,BMG_DS000937,,"Ectromelia, Infectious","Ectromelia, Infectious",,,,,,C0013591,D004482,,MONDO:0005809,infectious ectromelia,
+BMGC_DS00734,BMG_DS000938,155178000;62909004;127559009,Ectropion,Ectropion,,,,DOID:1570,ectropion,C0013592,D004483,MTHU037564,MONDO:0002043,ectropion,Ectropion | Ectropion (disorder) | Ectropion | Eversion of the eyelid | Eyelashes turned out | Eyelid turned out | Eyelid everted | Ectropion of eyelid (disorder) | Ectropion of eyelid | Ectropion | Everted margin (morphologic abnormality) | Everted margin
+BMGC_DS00735,BMG_DS000939,238538009;43116000;156326000,Eczema,Eczema,,,,,,C0013595,D004485,MTHU003535,,,Eczema | Dermatitis | Eczema (disorder) | Eczema | Eczema (disorder)
+BMGC_DS00736,BMG_DS000944,,Ehlers-Danlos Syndrome,Ehlers-Danlos Syndrome,,,,DOID:13359,Ehlers-Danlos syndrome,C0013720,D004535,,MONDO:0020066,Ehlers-Danlos syndrome,
+BMGC_DS00737,BMG_DS000946,,Elaeophoriasis,Filariasis,,,,,,C0013755,D005368,,,,
+BMGC_DS00738,BMG_DS000947,240820001;266334008;155485008,Elephantiasis,Elephantiasis,,,,DOID:0050138;DOID:4976,podoconiosis | elephantiasis,C0013882,D004604,,MONDO:0005424,elephantiasis,Lymphatic filariasis | Lymphatic filariasis (disorder) | Filarial elephantiasis | Elephantiasis | Elephantiasis | Lymphoedema | Lymphoedema NOS | (Elephantiasis) or (lymphoedema [& NOS]) | Lymphedema | Lymphedema NOS | (Elephantiasis) or (lymphedema [& NOS]) | (Elephantiasis) or (lymphoedema [& NOS]) (disorder) | (Elephantiasis) or (lymphoedema [& NOS]) | (Elephantiasis) or (lymphedema [& NOS]) | Elephantiasis | Lymphoedema NOS | Lymphoedema | Lymphedema | Lymphedema NOS | (Elephantiasis) or (lymphoedema [& NOS]) (disorder)
+BMGC_DS00739,BMG_DS000948,,Filarial Elephantiases,"Elephantiasis, Filarial",,,,DOID:12211,filarial elephantiasis,C0013884,D004605,,MONDO:0005761,filarial elephantiasis,
+BMGC_DS00740,BMG_DS000949,,"Elliptocytosis, Hereditary","Elliptocytosis, Hereditary",,,,DOID:2373,hereditary elliptocytosis,C0013902,D004612,,MONDO:0017319,hereditary elliptocytosis,
+BMGC_DS00741,BMG_DS000950,,Ellis-Van Creveld Syndrome,Ellis-Van Creveld Syndrome,,,,DOID:12714,Ellis-Van Creveld syndrome,C0013903,D004613,225500,MONDO:0009162,Ellis-van Creveld syndrome,
+BMGC_DS00742,BMG_DS000953,,Embryopathies,Fetal Diseases,,,,,,C0013949,D005315,,,,
+BMGC_DS00743,BMG_DS000954,,Empty Sella Syndrome,Empty Sella Syndrome,,,,DOID:3642,empty sella syndrome,C0014008,D004652,,MONDO:0006740,empty sella syndrome,
+BMGC_DS00744,BMG_DS000956,,"Empyema, Gallbladder",Cholecystitis,,,,,,C0014012,D002764,,,,
+BMGC_DS00745,BMG_DS000957,,"Empyema, Pleural","Empyema, Pleural",,,,DOID:3798,pleural empyema,C0014013,D016724,,MONDO:0018667,pleural empyema,
+BMGC_DS00746,BMG_DS000958,,"Empyema, Tuberculous","Empyema, Tuberculous",,,,DOID:14305,tuberculous empyema,C0014014,D004654,,MONDO:0005999,tuberculous empyema,
+BMGC_DS00747,BMG_DS000959,45170000;267682000,Encephalitis,Encephalitis,,,,DOID:9588,encephalitis,C0014038,D004660,MTHU007426,MONDO:0019956,encephalitis,Encephalitis | Encephalitis (disorder) | Myelitis | Encephalitis | Encephalitis/myelitis | Encephalitis &/or myelitis | Encephalitis &/or myelitis (disorder)
+BMGC_DS00748,BMG_DS000960,,,,,,,DOID:5225,von Economo's disease,C0014040,,,MONDO:0019384,encephalitis lethargica,
+BMGC_DS00749,BMG_DS000961,,"Encephalitis, California","Encephalitis, California",,,,DOID:0050118,La Crosse encephalitis,C0014053,D004670,,,,
+BMGC_DS00750,BMG_DS000962,,"Encephalitis, Central European","Encephalitis, Tick-Borne",,,,DOID:0050175,tick-borne encephalitis,C0014054,D004675,,,,
+BMGC_DS00751,BMG_DS000963,192687008;68197003,Arbovirus encephalitis,,,,,DOID:646,viral encephalitis,C0014055,,,,,Arbovirus encephalitis | Arboviral encephalitis | Arbovirus encephalitis (disorder) | Arbovirus encephalitis | Arbovirus encephalitis (disorder)
+BMGC_DS00752,BMG_DS000964,,Japanese Encephalitis,"Encephalitis, Japanese",,,,DOID:10844,Japanese encephalitis,C0014057,D004672,,MONDO:0019209,Japanese encephalitis,
+BMGC_DS00753,BMG_DS000966,,"Encephalomyelitis, Acute Disseminated","Encephalomyelitis, Acute Disseminated",,,,DOID:639,acute disseminated encephalomyelitis,C0014059,D004673,,MONDO:0019383,acute disseminated encephalomyelitis,
+BMGC_DS00754,BMG_DS000967,,"Encephalitis, St. Louis","Encephalitis, St. Louis",,,,DOID:10845,St. Louis encephalitis,C0014060,D004674,,MONDO:0005969,st. Louis encephalitis,
+BMGC_DS00755,BMG_DS000969,,,,,,,,,C0014065,,,MONDO:0017078,cephalocele,
+BMGC_DS00756,BMG_DS000971,,,,,,,,,C0014067,,,MONDO:0017080,occipital encephalocele,
+BMGC_DS00757,BMG_DS000972,58762006,Encephalomalacia,Encephalomalacia,,,,DOID:2034,encephalomalacia,C0014068,D004678,MTHU061960,MONDO:0006741,encephalomalacia,Encephalomalacia | Encephalomalacia (disorder)
+BMGC_DS00758,BMG_DS000973,62950007;267684004;192682002;154991009,Encephalomyelitis,Encephalomyelitis,,,,DOID:640,encephalomyelitis,C0014070,D004679,,MONDO:0005156,encephalomyelitis,"Encephalomyelitis | Encephalomyelitis (disorder) | Encephalomyelitis | Myalgic encephalomyelitis | Encephalitis/myelitis NOS | Encephalitis/myelitis: [NOS] or [encephalomyelitis & (myalgic)] | Encephalitis/myelitis: [NOS] or [encephalomyelitis & (myalgic)] (disorder) | Encephalitis &/or myelitis &/or encephalomyelitis &/or transverse myelitis | Encephalitis, myelitis and encephalomyelitis | Transverse myelitis | Myelitis | Encephalomyelitis | Encephalitis &/or myelitis &/or encephalomyelitis &/or transverse myelitis (disorder) | Encephalitis/myelitis: [NOS] or [encephalomyelitis & (myalgic)] | Myalgic encephalomyelitis | Encephalitis/myelitis NOS | Encephalomyelitis | Encephalitis/myelitis: [NOS] or [encephalomyelitis & (myalgic)] (disorder)"
+BMGC_DS00759,BMG_DS000976,,"Leukoencephalitis, Acute Hemorrhagic","Leukoencephalitis, Acute Hemorrhagic",,,,DOID:10992,acute hemorrhagic leukoencephalitis,C0014077,D004684,606752,MONDO:0011716,acute hemorrhagic leukoencephalitis,
+BMGC_DS00760,BMG_DS000977,89990001,Venezuelan equine encephalomyelitis,,,,,DOID:9584,Venezuelan equine encephalitis,C0014078,,,MONDO:0006005,Venezuelan equine encephalitis,Venezuelan equine encephalitis | Venezuelan equine fever | VEE | Venezuelan equine encephalomyelitis | VEE - Venezuelan equine encephalitis | Venezuelan equine encephalitis (disorder)
+BMGC_DS00761,BMG_DS000978,268274005;16535008;205469005,Enchondromatosis,Enchondromatosis,2E83.Z,Benign osteogenic tumour of unspecified site,Q78.4,DOID:0060221;DOID:0090015,Maffucci syndrome | Cenani-Lenz syndactyly syndrome,C0014084,D004687,166000,MONDO:0008145,Ollier disease,Multiple enchondromata | Congenital enchondromatosis | Ollier disease | Dyschondroplasia | Ollier's disease | Enchondromatosis | Enchondromatosis (disorder) | Osteochondromatosis syndrome | Osteochondromatosis syndrome (disorder) | Pseudochondroplasia | Enchondromatosis | Ollier's disease | Osteopathia striata | Hypochondroplasia | Chondrodystophy NEC | Chondrodysplasia | Dyschondroplasia | Multiple enchondromata | (Multi enchondromata) or (enchondromat) or (Ollier dis) or (chondrodysplas) or (chondrodystophy NEC) or (hypochondroplas) or (osteopath striata) or (pseudochondroplas) or (dyschondroplas) | (Multi enchondromata) or (enchondromat) or (Ollier dis) or (chondrodysplas) or (chondrodystophy NEC) or (hypochondroplas) or (osteopath striata) or (pseudochondroplas) or (dyschondroplas) (disorder)
+BMGC_DS00762,BMG_DS000979,33806008,Endarteritis,Endarteritis,,,,,,C0014100,D004692,,MONDO:0043576,endarteritis,Endarteritis | Endarteritis (disorder)
+BMGC_DS00763,BMG_DS000980,,,,,,,DOID:0050651,atrioventricular septal defect,C0014116,,,,,
+BMGC_DS00764,BMG_DS000981,,Endocardial Fibroelastosis,Endocardial Fibroelastosis,,,,DOID:12929,endocardial fibroelastosis,C0014117,D004695,226000,MONDO:0009169,endocardial fibroelastosis,
+BMGC_DS00765,BMG_DS000982,56819008,Endocarditis,Endocarditis,,,,DOID:10314,endocarditis,C0014118,D004696,,MONDO:0005025,endocarditis,Endocarditis | Endocarditis (disorder)
+BMGC_DS00766,BMG_DS000983,,Bacterial Endocarditis,"Endocarditis, Bacterial",,,,,,C0014121,D004697,,MONDO:0006669,bacterial endocarditis,
+BMGC_DS00767,BMG_DS000985,31354001;266654000;155980007,Endocervicitis,,,,,DOID:5757,endocervicitis,C0014127,,,MONDO:0003632,endocervicitis,Endocervicitis | Endocervicitis (disorder) | Cervicitis &/or endocervicitis | Endocervicitis | Cervicitis | Cervicitis/endocervicitis | Cervicitis &/or endocervicitis (disorder) | Cervicitis &/or endocervicitis | Endocervicitis | Cervicitis/endocervicitis | Cervicitis | Cervicitis &/or endocervicitis (disorder)
+BMGC_DS00768,BMG_DS000986,,Endocrine System Diseases,Endocrine System Diseases,,,,DOID:28,endocrine system disease,C0014130,D004700,,MONDO:0005151,endocrine system disorder,
+BMGC_DS00769,BMG_DS000987,,,,,,,DOID:170,endocrine gland cancer,C0014132,,,MONDO:0002082,endocrine gland neoplasm,
+BMGC_DS00770,BMG_DS000988,,,,,,,DOID:1911,endodermal sinus tumor,C0014145,,,MONDO:0005744,yolk sac tumor,
+BMGC_DS00771,BMG_DS000989,,,,,,,DOID:1380,endometrial cancer,C0014170,,,MONDO:0021251,endometrium neoplasm,
+BMGC_DS00772,BMG_DS000990,,Endometrial Hyperplasia,Endometrial Hyperplasia,,,,DOID:0080365,endometrial hyperplasia,C0014173,D004714,,MONDO:0041161,obsolete endometrial hyperplasia,
+BMGC_DS00773,BMG_DS000991,198246007;129103003;396224008;103677003;155988000;266588002;11871002,Endometriosis,Endometriosis,,,N80,DOID:289,endometriosis,C0014175,D004715,MTHU036719,MONDO:0005133,endometriosis,Endometriosis (& [adenomyosis]) | Adenomyosis - uterine endomet. | Endometriosis | Adenomyosis | Endometriosis (& [adenomyosis]) (disorder) | Endometriosis (clinical) | Endometriosis (disorder) | Endometriosis | Endometriosis (morphologic abnormality) | Endometriosis | Endometriosis | External endometriosis | Endometriosis (morphologic abnormality) | Endometriosis (& [adenomyosis]) | Adenomyosis - uterine endomet. | Adenomyosis | Endometriosis | Endometriosis (& [adenomyosis]) (disorder) | Endometriosis | Endometriosis (disorder) | Endometriosis (disorder) | Endometriosis
+BMGC_DS00774,BMG_DS000992,22611009,Endometriosis of fallopian tube,,GA10.B3,Endometriosis of fallopian tube,N80.2,DOID:11424,fallopian tube endometriosis,C0014177,,,MONDO:0001282,fallopian tube endometriosis,Endometriosis of fallopian tube | Endometriosis of fallopian tube (disorder)
+BMGC_DS00775,BMG_DS000993,78623009;266652001;155975003,Endometritis,Endometritis,,,,DOID:1002,endometritis,C0014179,D004716,,MONDO:0000918,endometritis,"Endometritis | Endometritis (disorder) | Endometritis (& [excluding cervix]) | Endometritis | Endometritis - excl. cervix | Endometritis, excluding cervix | Endometritis (& [excluding cervix]) (disorder)"
+BMGC_DS00776,BMG_DS000996,1847009,Endophthalmitis,Endophthalmitis,,,,DOID:4692,endophthalmitis,C0014236,D009877,,MONDO:0016047,endophthalmitis,Endophthalmitis | Endophthalmitis (disorder)
+BMGC_DS00777,BMG_DS000997,57100005,Parasitic endophthalmitis,,,,,DOID:1398,parasitic infectious disease,C0014238,,,MONDO:0024315,parasitic endophthalmitis,Parasitic endophthalmitis | Parasitic endophthalmitis (disorder)
+BMGC_DS00778,BMG_DS000998,80093006;155200004;267746003,Enophthalmos,Enophthalmos,9A20.Z,"Displacement of eyeball, unspecified",H05.4,DOID:11175,enophthalmos,C0014306,D015841,MTHU036831,,,Enophthalmos | Enophthalmia | Enophthalmos (disorder) | Disorders of the orbit (& [enophthalmos] or [exophthalmos]) | Enophthalmos | Orbit disorders | Disorders of the orbit | Exophthalmos | Disorders of the orbit (& [enophthalmos] or [exophthalmos]) (disorder) | Enophthalmos | Exophthalmos | Disorders of the orbit | Orbit disorders | Disorders of the orbit (& [enophthalmos] or [exophthalmos]) | Disorders of the orbit (& [enophthalmos] or [exophthalmos]) (disorder)
+BMGC_DS00779,BMG_DS000999,,Entamoebiasis,Entamoebiasis,,,,,,C0014324,D004749,,,,
+BMGC_DS00780,BMG_DS001001,126767009;64613007,Enteritis,Enteritis,,,,,,C0014335,D004751,MTHU033961,MONDO:0043579,enteritis,"Inflammatory disorder of intestine | Inflammatory disorder of intestine (disorder) | Enteritis | Enteritis, inflammatory disorder of small intestine | Inflammation of small intestine (disorder) | Enteritis of small intestine | Inflammation of small intestine"
+BMGC_DS00781,BMG_DS001004,,Enterobacteriaceae Infections,Enterobacteriaceae Infections,,,,,,C0014347,D004756,,,,
+BMGC_DS00782,BMG_DS001005,43752006;197010007,Enterocolitis,Enterocolitis,,,,,,C0014356,D004760,MTHU017872;226150,MONDO:0009172,enterocolitis,"Enterocolitis | Enterocolitis, inflammation involving both small intestine and colon | Inflammation of small intestine and colon (disorder) | Inflammation of small intestine and colon | (Gastroenteriti) or (enterocolitis) or (other non-infective inflammatory gastroenteritis and colitis) | Enterocolitis | Other non-infective inflammatory gastroenteritis and colitis | Gastroenteritis | (Gastroenteriti) or (enterocolitis) or (other non-infective inflammatory gastroenteritis and colitis) (disorder)"
+BMGC_DS00783,BMG_DS001006,,"Enterocolitis, Pseudomembranous","Enterocolitis, Pseudomembranous",,,,DOID:0060185,Clostridium difficile colitis,C0014358,D004761,,,,
+BMGC_DS00784,BMG_DS001009,,Enterovirus Infections,Enterovirus Infections,,,,,,C0014378,D004769,,MONDO:0005747,enterovirus infectious disease,
+BMGC_DS00785,BMG_DS001010,33168009;155177005;246821008,Entropion,Entropion,,,,DOID:12397,entropion,C0014390,D004774,MTHU004143,MONDO:0001519,entropion,Entropion | Eyelid inverted | Eyelashes turned in | Eyelid turned in | Entropion of eyelid | Folded in eyelid | Entropion of eyelid (disorder) | Entropion | Entropion (disorder)
+BMGC_DS00786,BMG_DS001011,139398002;154929003;68191002;268776008;162121000;8009008,Enuresis,Enuresis,,,,,,C0014394,D004775,MTHU037203,MONDO:0024290,enuresis,Enuresis | Enuresis (finding) | Enuresis (& [bedwetting]) | Bedwetting | Enuresis | Enuresis (& [bedwetting]) (disorder) | Enuresis | Bedwetting | Enuresis (& [bedwetting]) | Enuresis (& [bedwetting]) (disorder) | Bed wetting | Bedwetting | Nocturnal incontinence of urine | Wets bed | Nocturnal enuresis | Nocturnal enuresis (finding)
+BMGC_DS00787,BMG_DS001013,165524009;27955006;418928000,Eosinophilia,Eosinophilia,4B03.Z,"Eosinophilia, unspecified",D72.1,DOID:999,hypereosinophilic syndrome,C0014457,D004802,MTHU004968,,,Eosinophil count raised | Eosinophilia | Eosinophilic disorder | Eosinophilic leucocytosis | Eosinophilic leukocytosis | Eosinophil count raised (finding) | Eosinophilia | Eosinophilia (disorder) | Decreased blood eosinophil number | Blood eosinophil number below reference range | Blood eosinophil number below reference range (finding)
+BMGC_DS00788,BMG_DS001014,,"Eosinophilia, Tropical",Eosinophilia,,,,,,C0014458,D004802,,,,
+BMGC_DS00789,BMG_DS001017,,,,,,,DOID:4844,benign ependymoma,C0014474,,,MONDO:0016698,ependymoma,
+BMGC_DS00790,BMG_DS001018,10865002,Eperythrozoonosis,Mycoplasma Infections,,,,,,C0014476,D009175,,,,Eperythrozoonosis | Eperythrozoonosis (disorder)
+BMGC_DS00791,BMG_DS001020,268088003;156659008;73583000,Epicondylitis,,,,,DOID:14087,epicondylitis,C0014488,,,MONDO:0001875,epicondylitis,(Epicondylitis &/or tennis elbow) or (golfers' elbow) | Golfers' elbow | Tennis elbow - epicondylitis | Epicondylitis | Golfer's elbow | Tennis elbow | (Epicondylitis &/or tennis elbow) or (golfers' elbow) (disorder) | Golfers' elbow | Golfer's elbow | Tennis elbow | Epicondylitis | Tennis elbow - epicondylitis | (Epicondylitis &/or tennis elbow) or (golfers' elbow) | (Epicondylitis &/or tennis elbow) or (golfers' elbow) (disorder) | Epicondylitis | Epicondylitis (disorder)
+BMGC_DS00792,BMG_DS001021,60548004,Epidemic keratoconjunctivitis,,1D84.0,Conjunctivitis due to adenovirus,B30.0,DOID:13014,shipyard eye,C0014493,,,MONDO:0001615,epidemic keratoconjunctivitis,Epidemic keratoconjunctivitis | Shipyard eye | Epidemic keratoconjunctivitis (disorder) | Virus keratoconjunctivitis | EKC - epidemic keratoconjunctivitis
+BMGC_DS00793,BMG_DS001024,,Toxic Epidermal Necrolysis,Stevens-Johnson Syndrome,,,,,,C0014518,D013262,,MONDO:0019810,toxic epidermal necrolysis,
+BMGC_DS00794,BMG_DS001026,,,,,,,DOID:13777,epidermodysplasia verruciformis,C0014522,,,MONDO:0009176,epidermodysplasia verruciformis,
+BMGC_DS00795,BMG_DS001027,,,,,,,DOID:2730,epidermolysis bullosa,C0014527,,,MONDO:0006541,epidermolysis bullosa,
+BMGC_DS00796,BMG_DS001028,403065006,Epidermophytosis,Tinea,,,,,,C0014531,D014005,,,,Epidermophytosis | Epidermophyton floccosum infection | Tinea caused by Epidermophyton floccosum | Tinea caused by Epidermophyton floccosum (disorder)
+BMGC_DS00797,BMG_DS001029,31070006;155914009,Epididymitis,Epididymitis,,,N45.1,DOID:9402,epididymitis,C0014534,D004823,MTHU038084,MONDO:0004779,epididymitis,Epididymitis | Epididymitis (disorder)
+BMGC_DS00798,BMG_DS001030,,,,,,,DOID:3618,epidural spinal canal neoplasm,C0014536,,,MONDO:0002713,epidural spinal canal neoplasm,
+BMGC_DS00799,BMG_DS001031,80384002,Epiglottitis,Epiglottitis,,,,DOID:9398,epiglottitis,C0014541,D004826,MTHU078414,MONDO:0005753,epiglottitis,Epiglottitis | Epiglottitis (disorder)
+BMGC_DS00800,BMG_DS001032,267698007;84757009,Epilepsy,Epilepsy,,,,DOID:1826,epilepsy,C0014544,D004827,MTHU022799,MONDO:0005027,epilepsy,(Epilepsy) or (epileptic attack) | Attack - epileptic | Epileptic attack | Epilepsy | (Epilepsy) or (epileptic attack) (disorder) | Epilepsy | Epilepsy (disorder)
+BMGC_DS00801,BMG_DS001033,,"Epilepsies, Partial","Epilepsies, Partial",,,,DOID:2234,focal epilepsy,C0014547,D004828,,MONDO:0005384,focal epilepsy,
+BMGC_DS00802,BMG_DS001034,,"Epilepsy, Generalized","Epilepsy, Generalized",,,,DOID:1827,idiopathic generalized epilepsy,C0014548,D004829,,MONDO:0100574,generalized epilepsy,
+BMGC_DS00803,BMG_DS001035,,Tonic-Clonic Epilepsy,"Epilepsy, Tonic-Clonic",,,,DOID:7725,epilepsy with generalized tonic-clonic seizures,C0014549,D004830,,MONDO:0005754,epilepsy with generalized tonic-clonic seizures,
+BMGC_DS00804,BMG_DS001036,,Myoclonic Epilepsy,"Epilepsies, Myoclonic",,,,DOID:308,early myoclonic encephalopathy,C0014550,D004831,,,,
+BMGC_DS00805,BMG_DS001037,,Absence Epilepsy,"Epilepsy, Absence",,,,DOID:1825;DOID:0070309,absence epilepsy | childhood absence epilepsy,C0014553,D004832,,MONDO:0850093,absence epilepsy,
+BMGC_DS00806,BMG_DS001038,,"Epilepsy, Temporal Lobe","Epilepsy, Temporal Lobe",,,,DOID:3328,temporal lobe epilepsy,C0014556,D004833,,MONDO:0005115,temporal lobe epilepsy,
+BMGC_DS00807,BMG_DS001040,,Uncinate Epilepsy,"Epilepsy, Temporal Lobe",,,,,,C0014558,D004833,,,,
+BMGC_DS00808,BMG_DS001049,44653001;266005008;154305002,Erysipelas,Erysipelas,,,A46,DOID:11330,erysipelas,C0014733,D004886,MTHU037335,MONDO:0001266,erysipelas,Erysipelas | Patch of erysipelas | Erysipelas (disorder) | Infection caused by Erysipelothrix rhusiopathiae | Infection caused by Erysipelothrix insidiosa | Infection caused by Erysipelothrix rhusiopathiae (disorder) | Erysipelas | Erysipelas (disorder)
+BMGC_DS00809,BMG_DS001053,,Erythema Multiforme,Erythema Multiforme,,,,DOID:0050185,erythema multiforme,C0014742,D004892,,MONDO:0006545,erythema multiforme,
+BMGC_DS00810,BMG_DS001054,,Erythema Nodosum,Erythema Nodosum,,,,DOID:0080750,erythema nodosum,C0014743,D004893,,MONDO:0850231,erythema nodosum,
+BMGC_DS00811,BMG_DS001056,54792008;200762004,Erythematosquamous dermatosis,,,,,DOID:9097,erythematosquamous dermatosis,C0014747,,,MONDO:0006546,erythematosquamous dermatosis,Erythematosquamous dermatosis | Erythematosquamous dermatosis (disorder)
+BMGC_DS00812,BMG_DS001057,266185008;154314007;200726000;186393009;111797001;238418005,Erythrasma,Erythrasma,1C44,Nonpyogenic bacterial infections of the skin,L08.1,DOID:4131,erythrasma,C0014752,D004894,,MONDO:0002885,erythrasma,(Actinomycosis (& [infections]) or (erythrasma) | Erythrasma | Actinomycotic infections | Actinomycosis | (Actinomycosis (& [infections]) or (erythrasma) (disorder) | (Actinomycosis (& [infections]) or (erythrasma) | Actinomycosis | Erythrasma | Actinomycotic infections | (Actinomycosis (& [infections]) or (erythrasma) (disorder) | Erythrasma | Erythrasma (disorder) | Cutaneous actinomycosis | Trichomycosis axillaris | Erythrasma | (Cutaneous actinomycosis) or (erythrasma) or (trichomycosis axillaris) | (Cutaneous actinomycosis) or (erythrasma) or (trichomycosis axillaris) (disorder)
+BMGC_DS00813,BMG_DS001058,,"Erythroblastosis, Fetal","Erythroblastosis, Fetal",,,,DOID:1098,hemolytic disease of the fetus,C0014761,D004899,,MONDO:0006760,fetal erythroblastosis,
+BMGC_DS00814,BMG_DS001059,,"Erythroderma, Maculopapular",Parapsoriasis,,,,,,C0014799,D010267,,,,
+BMGC_DS00815,BMG_DS001061,238777005;37151006,Erythromelalgia,Erythromelalgia,,,I73.81,DOID:9240,erythromelalgia,C0014804,D004916,,MONDO:0016028,erythromelalgia,Erythromelalgia | Erythromelalgia (disorder) | Erythromelalgia | Weir Mitchell's disease | Erythralgia | Erythermalgia | Erythromelalgia (disorder)
+BMGC_DS00816,BMG_DS001062,,Primary Erythermalgia,Erythromelalgia,,,,,,C0014805,D004916,133020,MONDO:0007571,primary erythermalgia,
+BMGC_DS00817,BMG_DS001065,,Escherichia coli Infections,Escherichia coli Infections,,,,,,C0014836,D004927,,MONDO:0020920,escherichia coli infection,
+BMGC_DS00818,BMG_DS001066,,Esophageal Achalasia,Esophageal Achalasia,,,,DOID:9164,achalasia,C0014848,D004931,,MONDO:0008698,achalasia,
+BMGC_DS00819,BMG_DS001067,,,,,,,DOID:10485,esophageal atresia,C0014850,,,MONDO:0001044,esophageal atresia,
+BMGC_DS00820,BMG_DS001068,,Esophageal Diseases,Esophageal Diseases,,,,DOID:6050,esophageal disease,C0014852,D004935,,MONDO:0003749,esophageal disorder,
+BMGC_DS00821,BMG_DS001069,,,,,,,DOID:9192,dyskinesia of esophagus,C0014858,,,MONDO:0004729,dyskinesia of esophagus,
+BMGC_DS00822,BMG_DS001070,,,,,,,DOID:5041,esophageal cancer,C0014859,,,MONDO:0021355,neoplasm of esophagus,
+BMGC_DS00823,BMG_DS001072,,Esophageal Stenosis,Esophageal Stenosis,,,,,,C0014866,D004940,,,,
+BMGC_DS00824,BMG_DS001073,,Esophageal Varices,Esophageal and Gastric Varices,,,,,,C0014867,D004932,,MONDO:0001221,esophageal varices,
+BMGC_DS00825,BMG_DS001074,16761005;266498005;155673008,Esophagitis,Esophagitis,,,K20,DOID:11963,esophagitis,C0014868,D004941,MTHU018345,MONDO:0001409,esophagitis,Esophagitis | Oesophagitis | Esophagitis (disorder) | Esophagitis (& [reflux]) or esophageal reflux | Gastro-esophageal reflux | Esophageal reflux | Esophagitis | Reflux esophagitis | Oesophagitis (& [reflux]) or oesophageal reflux | Gastro-oesophageal reflux | Oesophagitis | Reflux oesophagitis | Oesophageal reflux | Oesophagitis (& [reflux]) or oesophageal reflux (disorder) | Esophagitis (& [reflux]) or esophageal reflux | Oesophagitis (& [reflux]) or oesophageal reflux | Gastro-esophageal reflux | Reflux esophagitis | Esophageal reflux | Esophagitis | Gastro-oesophageal reflux | Reflux oesophagitis | Oesophageal reflux | Oesophagitis | Oesophagitis (& [reflux]) or oesophageal reflux (disorder)
+BMGC_DS00826,BMG_DS001075,,Peptic Esophagitis,"Esophagitis, Peptic",,,,DOID:13976,peptic esophagitis,C0014869,D004942,,MONDO:0006896,peptic esophagitis,
+BMGC_DS00827,BMG_DS001076,16596007;155193001,Esotropia,Esotropia,9C80.0,Esotropia,H50.0,DOID:9840,esotropia,C0014877,D004948,MTHU036341,MONDO:0004896,esotropia,Esotropia | Convergent strabismus | Cross-eye | Esotropia (disorder) | Convergent squint | Esotropia | Esotropia (disorder)
+BMGC_DS00828,BMG_DS001078,,Ethmoid Sinusitis,Ethmoid Sinusitis,,,,DOID:9507,ethmoid sinusitis,C0015029,D015521,,MONDO:0005756,ethmoid sinusitis,
+BMGC_DS00829,BMG_DS001079,,Euthyroid Sick Syndromes,Euthyroid Sick Syndromes,,,,DOID:2856,euthyroid sick syndrome,C0015190,D005067,,MONDO:0006755,euthyroid sick syndrome,
+BMGC_DS00830,BMG_DS001080,,,,,,,DOID:0050486,exanthem,C0015230,,,MONDO:0006547,exanthem,
+BMGC_DS00831,BMG_DS001081,,Exanthema Subitum,Exanthema Subitum,,,,DOID:0050495,exanthema subitum,C0015231,D005077,,MONDO:0000337,exanthema subitum,
+BMGC_DS00832,BMG_DS001084,267746003;18265008;155200004,Exophthalmos,Exophthalmos,,,,,,C0015300,D005094,MTHU005786,MONDO:0004770,exophthalmos,Enophthalmos | Exophthalmos | Disorders of the orbit | Orbit disorders | Disorders of the orbit (& [enophthalmos] or [exophthalmos]) | Disorders of the orbit (& [enophthalmos] or [exophthalmos]) (disorder) | Exophthalmos | Exophthalmia | Proptosis | Exophthalmos (disorder) | Eye displaced forwards | Disorders of the orbit (& [enophthalmos] or [exophthalmos]) | Enophthalmos | Orbit disorders | Disorders of the orbit | Exophthalmos | Disorders of the orbit (& [enophthalmos] or [exophthalmos]) (disorder)
+BMGC_DS00833,BMG_DS001086,,,,,,,DOID:206,hereditary multiple exostoses,C0015306,,,MONDO:0005508,hereditary multiple osteochondromas,
+BMGC_DS00834,BMG_DS001087,155194007;399054005;75400001,Exotropia,Exotropia,9C80.1,Exotropia,H50.1,DOID:1143,exotropia,C0015310,D005099,MTHU036896,MONDO:0001286,exotropia,Exotropia | Exotropia (disorder) | Exotropia (disorder) | Exotropia | Divergent strabismus | External strabismus | Divergent squint | XT - Exotropia | Exotropia | Divergent concomitant strabismus | Divergent strabismus | External strabismus | Exotropia (disorder) | Divergent squint
+BMGC_DS00835,BMG_DS001089,,Extrapyramidal Disorders,Basal Ganglia Diseases,,,,,,C0015371,D001480,,,,
+BMGC_DS00836,BMG_DS001090,371405004;79517001,Disorder of eye,,,,,DOID:5614,eye disease,C0015397,,,MONDO:0002022,disorder of orbital region,Disorder of eye proper (disorder) | Disorder of eye | Disease of eyeball | Disorder of globe | Disorder of eyeball | Eye disorder | Disorder of eye proper | Disease of eye | Disease of eye (disorder)
+BMGC_DS00837,BMG_DS001091,,"Eye Diseases, Hereditary","Eye Diseases, Hereditary",,,,,,C0015398,D015785,,,,
+BMGC_DS00838,BMG_DS001092,,Eye Infection,Eye Infections,,,,,,C0015403,D015817,,MONDO:0043885,eye infectious disorder,
+BMGC_DS00839,BMG_DS001093,,"Eye Infections, Bacterial","Eye Infections, Bacterial",,,,,,C0015404,D015818,,,,
+BMGC_DS00840,BMG_DS001094,,,,,,,,,C0015405,,,MONDO:0020944,fungal infection of eye,
+BMGC_DS00841,BMG_DS001096,,"Eye Infections, Viral","Eye Infections, Viral",,,,,,C0015407,D015828,,MONDO:0020950,viral eye infection,
+BMGC_DS00842,BMG_DS001097,,,,,,,DOID:2174,ocular cancer,C0015414,,,MONDO:0021220,eye neoplasm,
+BMGC_DS00843,BMG_DS001098,,Eyelid Diseases,Eyelid Diseases,,,,DOID:530,eyelid disease,C0015423,D005141,,MONDO:0003382,eyelid disorder,
+BMGC_DS00844,BMG_DS001099,,,,,,,DOID:2173,eyelid benign neoplasm,C0015424,,,MONDO:0002235,eyelid neoplasm,
+BMGC_DS00845,BMG_DS001100,,Facial Dermatoses,Facial Dermatoses,,,,DOID:3134,facial dermatosis,C0015456,D005148,,MONDO:0006548,facial dermatosis,
+BMGC_DS00846,BMG_DS001101,,Facial Hemiatrophy,Facial Hemiatrophy,,,,DOID:1757,facial hemiatrophy,C0015458,D005150,141300,MONDO:0007710,facial hemiatrophy,
+BMGC_DS00847,BMG_DS001102,,Facial Nerve Diseases,Facial Nerve Diseases,,,,DOID:1756,facial nerve disease,C0015464,D005155,,MONDO:0002098,facial nerve disorder,
+BMGC_DS00848,BMG_DS001103,,Facial Neuralgia,Facial Neuralgia,,,,DOID:13865,facial neuralgia,C0015467,D005156,,MONDO:0001818,facial neuralgia,
+BMGC_DS00849,BMG_DS001104,,Facial paralysis,,,,,DOID:13934,facial paralysis,C0015469,,MTHU037394,MONDO:0001835,facial paralysis,
+BMGC_DS00850,BMG_DS001106,,,,,,,DOID:1766,factitious disorder,C0015481,,,,,
+BMGC_DS00851,BMG_DS001107,,,,,,,DOID:2216,factor V deficiency,C0015499,,227400,MONDO:0009210,congenital factor V deficiency,
+BMGC_DS00852,BMG_DS001108,,Factor VII Deficiency,Factor VII Deficiency,,,,DOID:2215,factor VII deficiency,C0015503,D005168,,MONDO:0002244,factor VII deficiency,
+BMGC_DS00853,BMG_DS001109,,Factor X Deficiency,Factor X Deficiency,,,,DOID:2222,factor X deficiency,C0015519,D005171,,MONDO:0002247,factor X deficiency,
+BMGC_DS00854,BMG_DS001110,,,,,,,DOID:2229,factor XI deficiency,C0015523,,612416,MONDO:0012897,congenital factor XI deficiency,
+BMGC_DS00855,BMG_DS001111,,Factor XII Deficiency,Factor XII Deficiency,,,,DOID:2231,factor XII deficiency,C0015526,D005175,234000,MONDO:0009315,congenital factor XII deficiency,
+BMGC_DS00856,BMG_DS001112,,,,,,,DOID:2211,factor XIII deficiency,C0015530,,,MONDO:0018029,congenital factor XIII deficiency,
+BMGC_DS00857,BMG_DS001113,,Failure to Thrive,Failure to Thrive,,,,,,C0015544,D005183,MTHU076871,,,
+BMGC_DS00858,BMG_DS001114,,Fallopian Tube Diseases,Fallopian Tube Diseases,,,,DOID:1962,fallopian tube disease,C0015556,D005184,,MONDO:0002156,fallopian tube disorder,
+BMGC_DS00859,BMG_DS001115,,,,,,,DOID:1964,fallopian tube cancer,C0015558,,,MONDO:0021092,fallopian tube neoplasm,
+BMGC_DS00860,BMG_DS001116,,Fanconi Syndrome,Fanconi Syndrome,,,,DOID:1062,Fanconi syndrome,C0015624,D005198,,MONDO:0001083,Fanconi renotubular syndrome,
+BMGC_DS00861,BMG_DS001117,,Fanconi Anemia,Fanconi Anemia,,,,DOID:13636,Fanconi anemia,C0015625,D005199,,MONDO:0019391,Fanconi anemia,
+BMGC_DS00862,BMG_DS001119,,Farmer's Lung,Farmer's Lung,,,,DOID:14453,farmer's lung,C0015634,D005203,,MONDO:0001971,farmer's lung disease,
+BMGC_DS00863,BMG_DS001120,,Fascicular Block,Bundle-Branch Block,,,,,,C0015643,D002037,,,,
+BMGC_DS00864,BMG_DS001121,36948007,Fasciitis,Fasciitis,,,,DOID:9598,fasciitis,C0015645,D005208,,MONDO:0004830,fasciitis,Fasciitis | Fasciitis (disorder)
+BMGC_DS00865,BMG_DS001122,187125007;111922007,Fascioliasis,Fascioliasis,1F82,Fascioliasis,B66.3,DOID:885,fascioliasis,C0015652,D005211,,MONDO:0004668,fascioliasis,Liver flukes NOS | Sheep liver fluke infection | Fascioliasis | (Fascioliasis) or (liver fluke: [sheep infection] or [NOS]) | (Fascioliasis) or (liver fluke: [sheep infection] or [NOS]) (disorder) | Infection by Fasciola | Fascioliasis | Infection caused by Fasciola | Infection caused by Fasciola (disorder)
+BMGC_DS00866,BMG_DS001123,,Fascioloidiasis,Fascioloidiasis,,,,DOID:1217,fascioloidiasis,C0015655,D005213,,MONDO:0005759,fascioloidiasis,
+BMGC_DS00867,BMG_DS001124,54266002,Fasciolopsiasis,Trematode Infections,1F83,Fasciolopsiasis,B66.5,DOID:888,fasciolopsiasis,C0015656,D014201,,MONDO:0004672,fasciolopsiasis,Infection by Fasciolopsis buski | Fasciolopsiasis | Giant intestinal fluke infection | Intestinal distomiasis | Fasciolopsiosis | Infection caused by Fasciolopsis buski (disorder) | Infection caused by Fasciolopsis buski
+BMGC_DS00868,BMG_DS001125,,Chronic Fatigue Syndrome,"Fatigue Syndrome, Chronic",,,,DOID:8544,chronic fatigue syndrome,C0015674,D015673,,MONDO:0005404,myalgic encephalomeyelitis/chronic fatigue syndrome,
+BMGC_DS00869,BMG_DS001126,,Fatty Liver,Fatty Liver,,,,DOID:9452,steatotic liver disease,C0015695,D005234,,,,
+BMGC_DS00870,BMG_DS001127,,"Fatty Liver, Alcoholic","Fatty Liver, Alcoholic",,,,DOID:9452,steatotic liver disease,C0015696,D005235,,MONDO:0021104,alcoholic fatty liver disease,
+BMGC_DS00871,BMG_DS001128,267558001;154801000;76500009;191172001,Favism,Favism,3A10.00,Haemolytic anaemia due to glucose6phosphate dehydrogenase deficiency,D55.0,DOID:13628,favism,C0015702,D005236,,MONDO:0001761,favism,Hereditary elliptocytosis | Hereditary stomatocytosis | Favism | Other hered. haem. anaemias | Other hered. hem. anemias | (Hereditary: [elliptocytosis] or [stomatocytosis] or [other haemalytic anaemias]) or (favism) | (Hereditary: [elliptocytosis] or [stomatocytosis] or [other hemalytic anemias]) or (favism) | (Hereditary: [elliptocytosis] or [stomatocytosis] or [other haemalytic anaemias]) or (favism) (disorder) | (Hereditary: [elliptocytosis] or [stomatocytosis] or [other haemalytic anaemias]) or (favism) | (Hereditary: [elliptocytosis] or [stomatocytosis] or [other hemalytic anemias]) or (favism) | Favism | Hereditary stomatocytosis | Hereditary elliptocytosis | Other hered. hem. anemias | Other hered. haem. anaemias | (Hereditary: [elliptocytosis] or [stomatocytosis] or [other haemalytic anaemias]) or (favism) (disorder) | Vicia faba poisoning | Vicia faba poisoning (disorder) | Favism | Favism (disorder)
+BMGC_DS00872,BMG_DS001129,,Favre-Racouchot Syndrome,Facial Dermatoses,,,,,,C0015704,D005148,,,,
+BMGC_DS00873,BMG_DS001130,,,,,,,,,C0015708,,211500,MONDO:0100428,progressive bulbar palsy of childhood,
+BMGC_DS00874,BMG_DS001131,,Fecal Incontinence,Fecal Incontinence,,,,,,C0015732,D005242,,,,
+BMGC_DS00875,BMG_DS001133,,Felty Syndrome,Felty Syndrome,,,,DOID:11042,Felty's syndrome,C0015773,D005258,134750,MONDO:0007603,Felty syndrome,
+BMGC_DS00876,BMG_DS001134,,,,,,,DOID:5546,femoral cancer,C0015807,,,MONDO:0021579,neoplasm of femur,
+BMGC_DS00877,BMG_DS001135,,Femur Head Necrosis,Femur Head Necrosis,,,,,,C0015814,D005271,,,,
+BMGC_DS00878,BMG_DS001136,,Fetal Alcohol Syndrome,Fetal Alcohol Spectrum Disorders,,,,,,C0015923,D063647,,MONDO:0016011,fetal alcohol syndrome,
+BMGC_DS00879,BMG_DS001137,,Fetal Diseases,Fetal Diseases,,,,,,C0015929,D005315,,,,
+BMGC_DS00880,BMG_DS001139,,,,,,,,,C0015934,,,MONDO:0005030,fetal growth restriction,
+BMGC_DS00881,BMG_DS001140,,Fetal Resorption,Fetal Resorption,,,,,,C0015951,D005327,,,,
+BMGC_DS00882,BMG_DS001141,,,,,,,DOID:1235,fetishism,C0015957,,,MONDO:0001504,fetishistic disorder,
+BMGC_DS00883,BMG_DS001144,,Breast Fibrocystic Disease,Fibrocystic Breast Disease,,,,DOID:10354,breast fibrocystic disease,C0016034,D005348,,MONDO:0005219,breast fibrocystic disease,
+BMGC_DS00884,BMG_DS001145,,Fibrodysplasia Ossificans Progressiva,Myositis Ossificans,,,,DOID:13374,fibrodysplasia ossificans progressiva,C0016037,D009221,135100,MONDO:0007606,fibrodysplasia ossificans progressiva,
+BMGC_DS00885,BMG_DS001147,,,,,,,,,C0016045,,,MONDO:0005167,fibroma,
+BMGC_DS00886,BMG_DS001148,,,,,,,,,C0016048,,,MONDO:0005031,fibromatosis,
+BMGC_DS00887,BMG_DS001149,,Fibromuscular Dysplasia,Fibromuscular Dysplasia,,,,,,C0016052,D005352,135580,MONDO:0006761,fibromuscular dysplasia,
+BMGC_DS00888,BMG_DS001150,247365004;203082005;1304004;156727006;24693007;203138004,Fibromyalgia,Fibromyalgia,MG30.01,Chronic widespread pain,M79.7,DOID:631,fibromyalgia,C0016053,D005356,MTHU038078,MONDO:0005546,fibromyalgia,Fibromyalgia | Fibromyalgia (finding) | Fibromyalgia | Fibromyalgia (disorder) | Fibromyositis | Fibromyositis (disorder)
+BMGC_DS00889,BMG_DS001151,,,,,,,DOID:3355,fibrosarcoma,C0016057,,,MONDO:0005164,fibrosarcoma,
+BMGC_DS00890,BMG_DS001152,,"Fibrous Dysplasia, Monostotic","Fibrous Dysplasia, Monostotic",,,,,,C0016064,D005358,,MONDO:0019665,monostotic fibrous dysplasia,
+BMGC_DS00891,BMG_DS001153,,,,,,,DOID:1858,McCune Albright syndrome,C0016065,,,MONDO:0008274,polyostotic fibrous dysplasia,
+BMGC_DS00892,BMG_DS001154,105706003;50342004,Filariasis,Filariasis,,,B74,DOID:1080,filariasis,C0016085,D005368,,MONDO:0016075,filariasis,Filariosis | Filariasis | Disease caused by Filarioidea (disorder) | Disease caused by Filarioidea | Filariasis | Filariosis | Filariasis (disorder)
+BMGC_DS00893,BMG_DS001156,,,,,,,DOID:12402,pyromania,C0016142,,,MONDO:0001522,pyromania,
+BMGC_DS00894,BMG_DS001157,,Fish Diseases,Fish Diseases,,,,,,C0016154,D005393,,MONDO:0024934,fish disease,
+BMGC_DS00895,BMG_DS001158,,Anal Fissure,Fissure in Ano,,,,,,C0016167,D005401,,,,
+BMGC_DS00896,BMG_DS001159,,,,,,,,,C0016202,,,MONDO:0005293,flatfoot,
+BMGC_DS00897,BMG_DS001160,,Focal Dermal Hypoplasia,Focal Dermal Hypoplasia,,,,DOID:2120,focal dermal hypoplasia,C0016395,D005489,305600,MONDO:0010592,focal dermal hypoplasia,
+BMGC_DS00898,BMG_DS001162,,"Epilepsy, Partial, Motor","Epilepsy, Partial, Motor",,,,DOID:3327,partial motor epilepsy,C0016399,D020938,,MONDO:0006891,partial motor epilepsy,
+BMGC_DS00899,BMG_DS001163,,Folic Acid Deficiency,Folic Acid Deficiency,,,,,,C0016412,D005494,,,,
+BMGC_DS00900,BMG_DS001165,13600006;156411003;267863007;201177005,Folliculitis,Folliculitis,,,,DOID:4409,folliculitis,C0016436,D005499,MTHU024866,MONDO:0006552,folliculitis,Folliculitis | Folliculitis (disorder) | Seborrhea capitis | (Folliculitis) or (seborrhoea capitis) | Seborrhoea capitis | (Folliculitis) or (seborrhea capitis) | Folliculitis | (Folliculitis) or (seborrhoea capitis) (disorder)
+BMGC_DS00901,BMG_DS001166,,Food Allergy,Food Hypersensitivity,,,,DOID:3044,food allergy,C0016470,D005512,,,,
+BMGC_DS00902,BMG_DS001167,,Foot Dermatoses,Foot Dermatoses,,,,,,C0016509,D005533,,,,
+BMGC_DS00903,BMG_DS001168,,Foot Diseases,Foot Diseases,,,,,,C0016510,D005534,,MONDO:0044989,obsolete foot disorder,
+BMGC_DS00904,BMG_DS001171,,"Foramen Ovale, Patent","Foramen Ovale, Patent",,,,DOID:13620,patent foramen ovale,C0016522,D054092,,MONDO:0020439,patent foramen ovale,
+BMGC_DS00905,BMG_DS001173,,Influenza in Birds,Influenza in Birds,,,,DOID:4492,avian influenza,C0016627,D005585,,MONDO:0018695,avian influenza,
+BMGC_DS00906,BMG_DS001175,254682006;65038009,Fox Fordyce disease,,,,,DOID:1381,Fox-Fordyce disease,C0016632,,,MONDO:0006553,Fox-Fordyce disease,Fox Fordyce disease | Fox Fordyce disease (disorder) | Fox-Fordyce disease | Apocrine miliaria | Fox Fordyce disease | Apocrine miliaria (disorder)
+BMGC_DS00907,BMG_DS001176,,Fragile X Syndrome,Fragile X Syndrome,,,,DOID:14261,fragile X syndrome,C0016667,D005600,300624,MONDO:0010383,fragile X syndrome,
+BMGC_DS00908,BMG_DS001178,,Freemartinism,Freemartinism,,,,DOID:4671,freemartinism,C0016697,D005611,,MONDO:0006762,freemartinism,
+BMGC_DS00909,BMG_DS001179,,Friedreich Ataxia,Friedreich Ataxia,,,,DOID:12705,Friedreich ataxia,C0016719,D005621,,MONDO:0100339,Friedreich ataxia,
+BMGC_DS00910,BMG_DS001180,,Froehlich's Syndrome,Hypothalamic Diseases,,,,DOID:6676,Froelich syndrome,C0016724,D007027,,MONDO:0003962,Froelich syndrome,
+BMGC_DS00911,BMG_DS001181,,Frontal Sinusitis,Frontal Sinusitis,,,,DOID:10791,frontal sinusitis,C0016735,D015522,,MONDO:0001121,frontal sinusitis,
+BMGC_DS00912,BMG_DS001182,,,,,,,DOID:9869,hereditary fructose intolerance syndrome,C0016751,,229600,MONDO:0009249,hereditary fructose intolerance,
+BMGC_DS00913,BMG_DS001184,,"Fructose-1,6-Diphosphatase Deficiency","Fructose-1,6-Diphosphatase Deficiency",,,,DOID:5204,"fructose-1,6-bisphosphatase deficiency",C0016756,D015319,229700,MONDO:0009251,"fructose-1,6-bisphosphatase deficiency",
+BMGC_DS00914,BMG_DS001185,,Fuchs Endothelial Dystrophy,Fuchs' Endothelial Dystrophy,,,,DOID:11555,Fuchs' endothelial dystrophy,C0016781,D005642,,MONDO:0005321,Fuchs' endothelial dystrophy,
+BMGC_DS00915,BMG_DS001186,11226001,Fuchs' heterochromic cyclitis,,,,H20.81,DOID:9375,Fuchs' heterochromic uveitis,C0016782,,,MONDO:0016989,Fuchs heterochromic iridocyclitis,Fuchs' heterochromic cyclitis | Fuchs' heterochromic uveitis | Fuchs' heterochromic iridocyclitis | Fuchs' heterochromic cyclitis (disorder) | Fuchs uveitis syndrome
+BMGC_DS00916,BMG_DS001187,,Fucosidase Deficiency Disease,Fucosidosis,,,,DOID:14500,fucosidosis,C0016788,D005645,230000,MONDO:0009254,fucosidosis,
+BMGC_DS00917,BMG_DS001188,81120009,Functional disorder of intestine,,,,,DOID:9779,bowel dysfunction,C0016807,,,,,Functional disorder of intestine | Functional disorder of intestine (disorder)
+BMGC_DS00918,BMG_DS001190,112650006,Furunculosis,Furunculosis,,,,,,C0016867,D005667,MTHU076074,MONDO:0025419,furunculosis,Furunculosis | Furunculosis (morphologic abnormality)
+BMGC_DS00919,BMG_DS001191,,,,,,,,,C0016873,,273000,MONDO:0010103,"teeth, fused",
+BMGC_DS00920,BMG_DS001193,,Galactosemias,Galactosemias,,,,DOID:9870,galactosemia,C0016952,D005693,,MONDO:0018116,galactosemia,
+BMGC_DS00921,BMG_DS001194,,Gall Bladder Diseases,Gallbladder Diseases,,,,DOID:0060262,gallbladder disease,C0016977,D005705,,MONDO:0005281,gallbladder disorder,
+BMGC_DS00922,BMG_DS001195,,,,,,,DOID:3121,gallbladder cancer,C0016978,,,MONDO:0021253,gallbladder neoplasm,
+BMGC_DS00923,BMG_DS001197,,Gangliosidoses,Gangliosidoses,,,,DOID:2368,gangliosidosis,C0017083,D005733,,MONDO:0017719,gangliosidosis,
+BMGC_DS00924,BMG_DS001198,36024000;372070002;263765007,Gangrene,Gangrene,,,,,,C0017086,D005734,MTHU037861,,,Gangrene | Gangrene (morphologic abnormality) | Gangrenous | Gangrenous disorder (disorder) | Gangrenous disorder | Gangrene | Gangrene | Gangrene (disorder)
+BMGC_DS00925,BMG_DS001199,,Gardner Syndrome,Gardner Syndrome,,,,,,C0017097,D005736,,MONDO:0019336,Gardner syndrome,
+BMGC_DS00926,BMG_DS001201,,Gastric Varix,Esophageal and Gastric Varices,,,,,,C0017145,D004932,,,,
+BMGC_DS00927,BMG_DS001202,,,,,,,DOID:5577,gastrinoma,C0017150,,,MONDO:0003523,gastrin-producing neuroendocrine tumor,
+BMGC_DS00928,BMG_DS001203,266503008;235653009;4556007;155711008,Gastritis,Gastritis,,,,DOID:4029,gastritis,C0017152,D005756,MTHU062400,MONDO:0004966,gastritis,Gastritis | Gastritis and duodenitis | Gastritis &/or duodenitis | Gastritis &/or duodenitis (disorder) | Gastritis | Gastritis (disorder) | Gastritis | Gastric catarrh | Gastritis (disorder) | Gastritis &/or duodenitis | Gastritis | Gastritis and duodenitis | Gastritis &/or duodenitis (disorder)
+BMGC_DS00929,BMG_DS001204,,"Gastritis, Atrophic","Gastritis, Atrophic",,,,DOID:8929,atrophic gastritis,C0017154,D005757,,MONDO:0006665,chronic atrophic gastritis,
+BMGC_DS00930,BMG_DS001205,,"Gastritis, Hypertrophic","Gastritis, Hypertrophic",,,,DOID:8757,gastric mucosal hypertrophy,C0017155,D005758,137280,MONDO:0007652,gastric mucosal hypertrophy,
+BMGC_DS00931,BMG_DS001206,25374005;197010007;266179001;154278002,Gastroenteritis,Gastroenteritis,,,,DOID:2326,gastroenteritis,C0017160,D005759,MTHU035020,MONDO:0002269,gastroenteritis,"Gastroenteritis | Gastroenteropathy | GE - Gastroenteritis | Inflammation of stomach and intestine | Inflammation of stomach and intestine (disorder) | (Gastroenteriti) or (enterocolitis) or (other non-infective inflammatory gastroenteritis and colitis) | Enterocolitis | Other non-infective inflammatory gastroenteritis and colitis | Gastroenteritis | (Gastroenteriti) or (enterocolitis) or (other non-infective inflammatory gastroenteritis and colitis) (disorder) | (Gastroenteritis (& [viral NOS])) or (vomiting: [viral] or [& diarrhoea infection]) or (gastric flu) | Diarrhea&vomiting, infection | Diarrhea+vomiting,infection | Diarrhoea+vomiting,infection | Diarrhoea&vomiting, infection | Vomiting - viral | Gastroenteritis | Gastroenteritis - viral + NOS | Gastric 'flu | Gastric flu | Viral vomiting | (Gastroenteritis (& [viral NOS])) or (vomiting: [viral] or [& diarrhea infection]) or (gastric flu) | (Gastroenteritis (& [viral NOS])) or (vomiting: [viral] or [& diarrhoea infection]) or (gastric flu) (disorder) | Diarrhea&vomiting, infection | Diarrhea+vomiting,infection | Diarrhoea+vomiting,infection | Diarrhoea&vomiting, infection | (Gastroenteritis (& [viral NOS])) or (vomiting: [viral] or [& diarrhoea infection]) or (gastric flu) | Gastroenteritis | Gastroenteritis - viral + NOS | Gastric 'flu | Vomiting - viral | Gastric flu | Viral vomiting | (Gastroenteritis (& [viral NOS])) or (vomiting: [viral] or [& diarrhea infection]) or (gastric flu) | (Gastroenteritis (& [viral NOS])) or (vomiting: [viral] or [& diarrhoea infection]) or (gastric flu) (disorder)"
+BMGC_DS00932,BMG_DS001207,,"Gastroenteritis, Transmissible, of Swine","Gastroenteritis, Transmissible, of Swine",,,,,,C0017162,D005761,,MONDO:0025420,"gastroenteritis, transmissible, of swine",
+BMGC_DS00933,BMG_DS001208,54856001;235595009,Gastroesophageal reflux disease,,,,,DOID:8534,gastroesophageal reflux disease,C0017168,,109350;MTHU001906,MONDO:0007186,gastroesophageal reflux disease,Gastroesophageal reflux disease | Gastresophageal reflux disease | Gastroesophageal reflux disease (disorder) | Gastroesophageal reflux disease | Gastro-esophageal reflux | GORD - Gastro-esophageal reflux disease | Gastro-esophageal reflux disease | GOR - Gastro-esophageal reflux | Gastro-oesophageal reflux disease | Gastro-oesophageal reflux | GORD - Gastro-oesophageal reflux disease | GOR - Gastro-oesophageal reflux | Gastroesophageal reflux disease (disorder) | GERD - Gastro-esophageal reflux disease | Gastrooesophageal reflux disease
+BMGC_DS00934,BMG_DS001209,,Gastrointestinal Diseases,Gastrointestinal Diseases,,,,,,C0017178,D005767,,,,
+BMGC_DS00935,BMG_DS001210,,,,,,,DOID:3119,gastrointestinal system cancer,C0017185,,,,,
+BMGC_DS00936,BMG_DS001211,,Gaucher Disease,Gaucher Disease,,,,DOID:1926,Gaucher's disease,C0017205,D005776,,MONDO:0018150,Gaucher disease,
+BMGC_DS00937,BMG_DS001212,367108003;39823006,Generalized atherosclerosis,,,,I70.91,DOID:2347,generalized atherosclerosis,C0017327,,,MONDO:0002275,generalized atherosclerosis,Generalised atherosclerosis | Generalized atherosclerosis | Generalised atherosclerosis (disorder) | Generalized atherosclerosis | Generalised atherosclerosis | Arteriopathy | Arteriopath | Generalized atherosclerosis (disorder)
+BMGC_DS00938,BMG_DS001213,,Generalized Nonconvulsive Seizure Disorder,"Epilepsy, Generalized",,,,,,C0017332,D004829,,,,
+BMGC_DS00939,BMG_DS001215,,Geniculate Ganglionitis,Facial Nerve Diseases,,,,DOID:14075,geniculate ganglionitis,C0017407,D005155,,MONDO:0001873,geniculate ganglionitis,
+BMGC_DS00940,BMG_DS001216,,Herpes Zoster Oticus,Herpes Zoster Oticus,,,,DOID:9210,herpes zoster oticus,C0017409,D016697,,MONDO:0005769,geniculate herpes zoster,
+BMGC_DS00941,BMG_DS001217,,Female Genital Diseases,"Genital Diseases, Female",,,,DOID:229,female reproductive system disease,C0017411,D005831,,,,
+BMGC_DS00942,BMG_DS001218,,"Genital Diseases, Male","Genital Diseases, Male",,,,DOID:48,male reproductive system disease,C0017412,D005832,,,,
+BMGC_DS00943,BMG_DS001219,,,,,,,DOID:120,female reproductive organ cancer,C0017416,,,MONDO:0021148,female reproductive system neoplasm,
+BMGC_DS00944,BMG_DS001220,,,,,,,DOID:3856,male reproductive organ cancer,C0017417,,,MONDO:0024582,male reproductive system neoplasm,
+BMGC_DS00945,BMG_DS001221,58433006;186847001,Primary genital syphilis,,1A61.0,Primary genital syphilis,A51.0,,,C0017418,,,,,Primary genital syphilis | Primary genital syphilis (disorder) | Primary genital syphilis | Genital chancre | Primary genital syphilis (disorder)
+BMGC_DS00946,BMG_DS001222,13969006;187105008,Geotrichosis,Geotrichosis,1F2Y,Other specified mycoses,B48.3,DOID:2832,geotrichosis,C0017455,D005847,,MONDO:0005772,geotrichosis,Geotrichosis | Infection by Geotrichum | Geotrichosis (disorder) | Geotrichosis | Geotrichosis (disorder)
+BMGC_DS00947,BMG_DS001223,,,,,,,DOID:4969,Gerstmann syndrome,C0017494,,,MONDO:0005773,Gerstmann syndrome,
+BMGC_DS00948,BMG_DS001224,,Gerstmann-Straussler-Scheinker Disease,Gerstmann-Straussler-Scheinker Disease,,,,DOID:4249,Gerstmann-Straussler-Scheinker syndrome,C0017495,D016098,137440,MONDO:0007656,Gerstmann-Straussler-Scheinker syndrome,
+BMGC_DS00949,BMG_DS001225,,,,,,,DOID:200,benign giant cell tumor,C0017525,,,MONDO:0002171,giant cell tumor,
+BMGC_DS00950,BMG_DS001226,207036003;69484003,Angiolymphoid hyperplasia,,,,,DOID:0111157,Castleman disease,C0017531,,,MONDO:0015564,Castleman disease,Angiofollicular lymph node hyperplasia | Benign angiofollicular hyperplasia | Castleman's disease | Angiolymphoid hyperplasia | Castleman's disease (disorder) | Angiomatous lymphoid hamartoma | Castleman disease | Giant lymph node hyperplasia | Angiofollicular lymph node hyperplasia | Angiofollicular lymph node hyperplasia (disorder)
+BMGC_DS00951,BMG_DS001227,266075009;266176008;58265007,Giardiasis,Giardiasis,,,,DOID:10718,giardiasis,C0017536,D005873,,MONDO:0001103,giardiasis,Giardiasis | Giardiasis (disorder) | Giardial colitis | Colitis - giardial | Lambliasis | Giardiasis | Giardiasis (& [colitis]) | Giardiasis (& [colitis]) (disorder) | Giardiasis | Giardiosis | Giardiasis (disorder)
+BMGC_DS00952,BMG_DS001228,267480001;154698000;80849007,Gigantism,Gigantism,,,,,,C0017547,D005877,,MONDO:0020479,pituitary gigantism,"(Acromegaly &/or gigantism) or (pituitary hyperfunction, ant.) | Gigantism and acromegaly | Anterior pituitary hyperfunction | Acromegaly and gigantism | Acromegaly | Gigantism | Pituitary hyperfunction (ant.) | (Acromegaly &/or gigantism) or (pituitary hyperfunction, ant.) (disorder) | Gigantism and acromegaly | Acromegaly and gigantism | Acromegaly | Gigantism | Pituitary hyperfunction (ant.) | Anterior pituitary hyperfunction | (Acromegaly &/or gigantism) or (pituitary hyperfunction, ant.) | (Acromegaly &/or gigantism) or (pituitary hyperfunction, ant.) (disorder) | Gigantism | Normal giant | Genetic giant | Primordial giant | Giant | Giantism | Gigantism (disorder)"
+BMGC_DS00953,BMG_DS001229,,Gilbert Disease,Gilbert Disease,,,,DOID:2739,Gilbert syndrome,C0017551,D005878,143500,MONDO:0007745,Gilbert syndrome,
+BMGC_DS00954,BMG_DS001230,,Gingival Diseases,Gingival Diseases,,,,DOID:1483,gingival disease,C0017563,D005882,,MONDO:0002021,gingival disorder,
+BMGC_DS00955,BMG_DS001231,,Gingival Hypertrophy,Gingival Hypertrophy,,,,DOID:5338,gingival hypertrophy,C0017567,D005886,,MONDO:0003397,gingival hypertrophy,
+BMGC_DS00956,BMG_DS001233,,,,,,,DOID:1134,gingival recession,C0017572,,,MONDO:0001268,gingival recession,
+BMGC_DS00957,BMG_DS001234,196355002;66383009,Gingivitis,Gingivitis,,,,DOID:3087,gingivitis,C0017574,D005891,MTHU007445,MONDO:0002508,gingivitis,Gingivitis | Chronic gingivitis | Gingivitis (& [chronic]) | Gingivitis (& [chronic]) (disorder) | Gingivitis | Gingivitis (disorder)
+BMGC_DS00958,BMG_DS001235,,,,,,,DOID:13924,necrotizing ulcerative gingivitis,C0017575,,,MONDO:0006865,necrotizing ulcerative gingivitis,
+BMGC_DS00959,BMG_DS001238,23986001;155120009;194631001,Glaucoma,Glaucoma,,,H40,DOID:1686,glaucoma,C0017601,D005901,MTHU004639,MONDO:0005041,glaucoma,Glaucoma | Glaucoma (disorder)
+BMGC_DS00960,BMG_DS001239,,Angle Closure Glaucoma,"Glaucoma, Angle-Closure",,,,DOID:13550,angle-closure glaucoma,C0017605,D015812,,MONDO:0001744,angle-closure glaucoma,
+BMGC_DS00961,BMG_DS001240,42456004;392288006;270882001;155123006;193544008,Primary angle-closure glaucoma,,9C61.1Z,"Primary angle closure and angle closure glaucoma, unspecified",H40.2,DOID:1405,primary angle-closure glaucoma,C0017606,,,MONDO:0001868,primary angle-closure glaucoma,Primary angle-closure glaucoma | Primary angle-closure glaucoma (disorder) | Primary angle-closure glaucoma (disorder) | Primary angle-closure glaucoma | Primary angle-closure glaucoma | ACG - Angle-closure glaucoma | Angle-closure glaucoma | Primary angle-closure glaucoma (disorder) | Glaucoma: [primary angle-closure] or [closed angle] | Primary angle-closure glaucoma | Closed angle glaucoma | Closed-angle glaucoma | Glaucoma: [primary angle-closure] or [closed angle] (disorder)
+BMGC_DS00962,BMG_DS001241,,"Glaucoma, Neovascular","Glaucoma, Neovascular",,,,DOID:1687,neovascular glaucoma,C0017609,D015355,,MONDO:0019783,neovascular glaucoma,
+BMGC_DS00963,BMG_DS001242,,"Glaucoma, Open-Angle","Glaucoma, Open-Angle",,,,DOID:1067,open-angle glaucoma,C0017612,D005902,,MONDO:0005338,open-angle glaucoma,
+BMGC_DS00964,BMG_DS001243,,"Glaucoma, Suspect",Ocular Hypertension,,,,,,C0017614,D009798,,,,
+BMGC_DS00965,BMG_DS001244,,,,,,,DOID:3068,glioblastoma,C0017636,,,MONDO:0018177,glioblastoma,
+BMGC_DS00966,BMG_DS001245,,,,,,,DOID:3070,high grade glioma,C0017638,,,MONDO:0021042,glioma,
+BMGC_DS00967,BMG_DS001246,,,,,,,DOID:2431,glomus tumor,C0017653,,,MONDO:0018327,glomus tumor,
+BMGC_DS00968,BMG_DS001248,36171008,Glomerulonephritis,Glomerulonephritis,,,N08,DOID:2921,glomerulonephritis,C0017658,D005921,MTHU036986,MONDO:0002462,glomerulonephritis,Glomerulonephritis | Glomerulonephritis (disorder) | GN - Glomerulonephritis
+BMGC_DS00969,BMG_DS001249,,IGA Glomerulonephritis,"Glomerulonephritis, IGA",,,,DOID:2986,IgA glomerulonephritis,C0017661,D005922,,MONDO:0005342,IgA glomerulonephritis,
+BMGC_DS00970,BMG_DS001250,,"Glomerulonephritis, Membranoproliferative","Glomerulonephritis, Membranoproliferative",,,,DOID:2920,membranoproliferative glomerulonephritis,C0017662,D015432,,MONDO:0002461,membranoproliferative glomerulonephritis,
+BMGC_DS00971,BMG_DS001251,77182004;197710000,Membranous glomerulonephritis,,,,,DOID:10976,membranous glomerulonephritis,C0017665,,MTHU069736,MONDO:0005376,membranous glomerulonephritis,"Membranous glomerulonephritis | Membranous glomerulonephritis (disorder) | MGN - Membranous glomerulonephritis | Chronic nephritic syndrome, diffuse membranous glomerulonephritis | Membranous glomerulonephritis | Membranous glomerulonephritis (disorder)"
+BMGC_DS00972,BMG_DS001252,25821008,Focal glomerulosclerosis,,,,,DOID:1312,focal segmental glomerulosclerosis,C0017668,,MTHU023216,MONDO:0100313,focal segmental glomerulosclerosis,Focal glomerular sclerosis | Focal glomerulosclerosis | Focal glomerular sclerosis (disorder) | FGS - Focal glomerulosclerosis
+BMGC_DS00973,BMG_DS001255,45534005;155666003,Glossitis,Glossitis,DA03.0,Glossitis,K14.0,DOID:1456,glossitis,C0017675,D005928,MTHU037108,MONDO:0006771,glossitis,Glossitis | Inflammation of tongue | Glossitis (disorder) | Glossitis | Glossitis (disorder)
+BMGC_DS00974,BMG_DS001256,,"Glossitis, Benign Migratory","Glossitis, Benign Migratory",,,,DOID:1455,geographic tongue,C0017677,D005929,,MONDO:0005771,geographic tongue,
+BMGC_DS00975,BMG_DS001257,,,,,,,,,C0017689,,,MONDO:0019959,glucagonoma,
+BMGC_DS00976,BMG_DS001258,,Glycogen Storage Disease,Glycogen Storage Disease,,,,DOID:2747,glycogen storage disease,C0017919,D006008,,MONDO:0002412,disorder of glycogen metabolism,
+BMGC_DS00977,BMG_DS001259,,Glycogen Storage Disease Type I,Glycogen Storage Disease Type I,,,,DOID:0081329,glycogen storage disease I,C0017920,D005953,,MONDO:0002413,glycogen storage disease I,
+BMGC_DS00978,BMG_DS001260,237967002,Glycogen storage disease type II,,,,,DOID:2752,glycogen storage disease II,C0017921,,232300,MONDO:0009290,glycogen storage disease II,"AMD - Acid maltase deficiency | alpha-Glucosidase deficiency | Glycogen storage disease type II | alpha-1,4-Glucosidase deficiency | Lysosomal alpha-1,4-glucosidase deficiency | Acid maltase deficiency | Lysosomal alpha-1,4-glucosidase deficiency (disorder)"
+BMGC_DS00979,BMG_DS001261,,Glycogen Storage Disease Type III,Glycogen Storage Disease Type III,,,,DOID:2748,glycogen storage disease III,C0017922,D006010,232400,MONDO:0009291,glycogen storage disease III,
+BMGC_DS00980,BMG_DS001262,,Glycogen Storage Disease Type IV,Glycogen Storage Disease Type IV,,,,DOID:2750,glycogen storage disease IV,C0017923,D006011,232500,MONDO:0009292,glycogen storage disease due to glycogen branching enzyme deficiency,
+BMGC_DS00981,BMG_DS001263,,Glycogen Storage Disease Type V,Glycogen Storage Disease Type V,,,,DOID:2746,glycogen storage disease V,C0017924,D006012,232600,MONDO:0009293,glycogen storage disease V,
+BMGC_DS00982,BMG_DS001264,,Glycogen Storage Disease Type VI,Glycogen Storage Disease Type VI,,,,DOID:2754,glycogen storage disease VI,C0017925,D006013,232700,MONDO:0009294,glycogen storage disease VI,
+BMGC_DS00983,BMG_DS001265,,Glycogen Storage Disease Type VII,Glycogen Storage Disease Type VII,,,,DOID:11721,glycogen storage disease VII,C0017926,D006014,232800,MONDO:0009295,glycogen storage disease VII,
+BMGC_DS00984,BMG_DS001266,,Glycogen Storage Disease Type VIII,Glycogen Storage Disease Type VIII,,,,DOID:2751,glycogen storage disease VIII,C0017927,D006015,,,,
+BMGC_DS00985,BMG_DS001267,,,,,,,DOID:9432,renal glycosuria,C0017980,,,,,
+BMGC_DS00986,BMG_DS001268,44086001,Gnathostomiasis,Gnathostomiasis,1F67,Gnathostomiasis,B83.1,DOID:11379,gnathomiasis,C0018013,D058429,,MONDO:0005776,gnathomiasis,Infection by Gnathostoma | Gnathostomiasis | Gnathomiasis | Gnathostomosis | Infection caused by Gnathostoma (disorder) | Infection caused by Gnathostoma
+BMGC_DS00987,BMG_DS001270,3716002;237568003,Goiter,Goiter,,,,DOID:12176,goiter,C0018021,D006042,MTHU001215,MONDO:0005397,goiter,Goiter | Enlargement of thyroid | Struma of thyroid | Thyromegaly | Goitre | Swelling of thyroid gland | Thyroid enlargement | Struma - goitre | Struma - goiter | Goiter (disorder) | Thyroid goiter | Thyroid goitre | Goitre | Goiter | Goitre (disorder)
+BMGC_DS00988,BMG_DS001271,56805008;271949009,Endemic goiter,,,,,DOID:13198,endemic goiter,C0018022,,,MONDO:0006742,endemic goiter,Endemic goiter | Simple iodine deficiency goiter | Simple iodine deficiency goitre | Endemic goitre | Endemic goiter (disorder) | Iodine-deficiency-related diffuse (endemic) goitre | Iodine-deficiency-related endemic goitre | Iodine-deficiency-related diffuse (endemic) goiter | Iodine-deficiency-related endemic goiter | Iodine-deficiency-related endemic goiter (disorder)
+BMGC_DS00989,BMG_DS001272,,Nodular Goiter,"Goiter, Nodular",,,,DOID:13197,nodular goiter,C0018023,D006044,,MONDO:0006869,nodular goiter,
+BMGC_DS00990,BMG_DS001273,66392007,Substernal goiter,,,,,DOID:13200,substernal goiter,C0018024,,,MONDO:0006986,substernal goiter,Substernal goiter | Intrathoracic goiter | Substernal goitre | Intrathoracic goitre | Substernal goiter (disorder) | Retrosternal goitre | Retrosternal goiter | Substernal thyroid goiter
+BMGC_DS00991,BMG_DS001274,,"Hypertension, Goldblatt","Hypertension, Renovascular",,,,,,C0018036,D006978,,,,
+BMGC_DS00992,BMG_DS001275,,Gonadal Disorders,Gonadal Disorders,,,,DOID:2277,gonadal disease,C0018050,D006058,,MONDO:0002259,gonadal disorder,
+BMGC_DS00993,BMG_DS001276,,,,,,,DOID:14447,gonadal dysgenesis,C0018051,,,MONDO:0001967,gonadal dysgenesis,
+BMGC_DS00994,BMG_DS001277,,"Gonadal Dysgenesis, 46,XY","Gonadal Dysgenesis, 46,XY",,,,DOID:14448,"46,XY sex reversal",C0018054,D006061,,,,
+BMGC_DS00995,BMG_DS001278,,"Gonadal Dysgenesis, Mixed","Gonadal Dysgenesis, Mixed",,,,DOID:14449,mixed gonadal dysgenesis,C0018055,D006060,,MONDO:0001969,mixed gonadal dysgenesis,
+BMGC_DS00996,BMG_DS001283,186943001;15628003,Gonorrhea,Gonorrhea,,,,DOID:7551,gonorrhea,C0018081,D006069,,MONDO:0004277,gonorrhea,Gonorrhea | Gonorrhoea | (Gonococcal infections NOS) or (gonorrhea) | (Gonococcal infections NOS) or (gonorrhoea) | Gonococcal infections NOS | (Gonococcal infections NOS) or (gonorrhoea) (disorder) | Gonorrhea | Gonococcal infection | Infection due to Neisseria gonorrhoeae | Gonorrhoea | Gonorrhea (disorder) | GC - Gonococcus infection | Clap | GCI - Gonococcal infection
+BMGC_DS00997,BMG_DS001284,90560007,Gout,Gout,,,M10,DOID:13189,gout,C0018099,D006073,MTHU037100,MONDO:0005393,gout,Gout | Gout (disorder)
+BMGC_DS00998,BMG_DS001286,,Graft-vs-Host Disease,Graft vs Host Disease,,,,DOID:0081267,graft-versus-host disease,C0018133,D006086,,MONDO:0013730,graft versus host disease,
+BMGC_DS00999,BMG_DS001287,,"Granular Dystrophy, Corneal","Corneal Dystrophies, Hereditary",,,,DOID:12318,granular corneal dystrophy,C0018179,D003317,,MONDO:0001490,corneal granular dystrophy,
+BMGC_DS01000,BMG_DS001288,,Granuloma Inguinale,Granuloma Inguinale,,,,DOID:9113,granuloma inguinale,C0018190,D006100,,MONDO:0005777,granuloma inguinale,
+BMGC_DS01001,BMG_DS001290,,,,,,,DOID:9072,lethal midline granuloma,C0018197,,,MONDO:0006828,nasal cavity and paranasal sinus lethal midline granuloma,
+BMGC_DS01002,BMG_DS001291,,"Granuloma, Respiratory Tract","Granuloma, Respiratory Tract",,,,,,C0018200,D015769,,,,
+BMGC_DS01003,BMG_DS001292,,Granulomatous Angiitis,"Vasculitis, Central Nervous System",,,,DOID:2555,granulomatous angiitis,C0018202,D020293,,MONDO:0002341,granulomatous angiitis,
+BMGC_DS01004,BMG_DS001293,191354002;387759001;11210002,Chronic granulomatous disease,,,,,DOID:3265,chronic granulomatous disease,C0018203,,,MONDO:0018305,chronic granulomatous disease,Chronic granulomatous disease | Chronic granulomatous disease (disorder) | Chronic granulomatous disease (disorder) | Chronic granulomatous disease | Congenital dysphagocytosis | CGD - Chronic granulomatous disease | Chronic granulomatous disease | Granulomatous disease | Congenital dysphagocytosis | CGD - Chronic granulomatous disease | Chronic granulomatous disease (disorder)
+BMGC_DS01005,BMG_DS001295,,,,,,,DOID:2999,granulosa cell tumor,C0018206,,,MONDO:0006036,granulosa cell tumor,
+BMGC_DS01006,BMG_DS001296,,Graves Disease,Graves Disease,,,,DOID:12361,Graves' disease,C0018213,D006111,,MONDO:0005364,Graves disease,
+BMGC_DS01007,BMG_DS001297,,Groenouw's Dystrophies,"Corneal Dystrophies, Hereditary",,,,,,C0018245,D003317,,,,
+BMGC_DS01008,BMG_DS001298,,Guillain-Barre Syndrome,Guillain-Barre Syndrome,,,,DOID:12842,Guillain-Barre syndrome,C0018378,D020275,,MONDO:0016218,Guillain-Barre syndrome,
+BMGC_DS01009,BMG_DS001299,,Gynatresia,Gynatresia,,,,DOID:429,gynatresia,C0018414,D006175,,MONDO:0002946,gynatresia,
+BMGC_DS01010,BMG_DS001300,155963008;4754008;266646002;198112004,Gynecomastia,Gynecomastia,,,N62,DOID:12698,gynecomastia,C0018418,D006177,MTHU006965,MONDO:0001571,gynecomastia disorder,(Breasts enlarged) or (hypertrophy) or (gynecomastia) | Enlarged breasts | Hypertrophy - breast | Breast hypertrophy | Breasts enlarged | (Breasts enlarged) or (hypertrophy) or (gynaecomastia) | Gynaecomastia | Gynecomastia | (Breasts enlarged) or (hypertrophy) or (gynaecomastia) (disorder) | Gynecomastia | Hypertrophy of male breast | Gynaecomastia | Gynaecomazia | Gynecomazia | Gynecomastia (disorder) | (Breasts enlarged) or (hypertrophy) or (gynecomastia) | Breasts enlarged | Hypertrophy - breast | Enlarged breasts | Breast hypertrophy | Gynaecomastia | (Breasts enlarged) or (hypertrophy) or (gynaecomastia) | Gynecomastia | (Breasts enlarged) or (hypertrophy) or (gynaecomastia) (finding) | Gynecomastia (& [bilateral] or [unilateral]) | Bilateral gynecomastia | Unilateral gynecomastia | Gynecomastia | Gynaecomastia (& [bilateral] or [unilateral]) | Gynaecomastia | Bilateral gynaecomastia | Unilateral gynaecomastia | Gynaecomastia (& [bilateral] or [unilateral]) (disorder)
+BMGC_DS01011,BMG_DS001301,,Gyrate Atrophy,Gyrate Atrophy,,,,DOID:1415,gyrate atrophy,C0018425,D015799,258870,MONDO:0009796,ornithine aminotransferase deficiency,
+BMGC_DS01012,BMG_DS001304,,Haemonchiasis,Haemonchiasis,,,,DOID:3332,haemonchiasis,C0018477,D006188,,MONDO:0005778,haemonchiasis,
+BMGC_DS01013,BMG_DS001305,,Haemophilus Infections,Haemophilus Infections,,,,,,C0018482,D006192,,MONDO:0006926,haemophilus infectious disease,
+BMGC_DS01014,BMG_DS001306,,Hair Diseases,Hair Diseases,,,,DOID:421,hair disease,C0018500,D006201,,,,
+BMGC_DS01015,BMG_DS001308,,Hallermann's Syndrome,Hallermann's Syndrome,,,,DOID:4534,Hallermann-Streiff syndrome,C0018522,D006210,234100,MONDO:0009318,Hallermann-Streiff syndrome,
+BMGC_DS01016,BMG_DS001309,,Hallervorden-Spatz Syndrome,Pantothenate Kinase-Associated Neurodegeneration,,,,DOID:3981,pantothenate kinase-associated neurodegeneration,C0018523,D006211,234200,MONDO:0009319,pantothenate kinase-associated neurodegeneration,
+BMGC_DS01017,BMG_DS001310,,,,,,,DOID:12797,hallucinogen abuse,C0018526,,,MONDO:0001585,hallucinogen abuse,
+BMGC_DS01018,BMG_DS001311,,,,,,,DOID:9977,hallucinogen dependence,C0018528,,,MONDO:0004939,hallucinogen dependence,
+BMGC_DS01019,BMG_DS001313,,,,,,,,,C0018552,,,MONDO:0006499,hamartoma,
+BMGC_DS01020,BMG_DS001314,,,,,,,DOID:6457,Cowden syndrome,C0018553,,,MONDO:0016063,Cowden disease,
+BMGC_DS01021,BMG_DS001315,,Hand Dermatoses,Hand Dermatoses,,,,DOID:3158,hand dermatosis,C0018567,D006229,,MONDO:0006556,hand dermatosis,
+BMGC_DS01022,BMG_DS001316,,"Hand, Foot and Mouth Disease","Hand, Foot and Mouth Disease",,,,DOID:10881,"hand, foot and mouth disease",C0018572,D006232,,MONDO:0005779,"hand, foot and mouth disease",
+BMGC_DS01023,BMG_DS001317,,Hartnup Disease,Hartnup Disease,,,,DOID:1060,Hartnup disease,C0018609,D006250,234500,MONDO:0009324,Hartnup disease,
+BMGC_DS01024,BMG_DS001318,,Hashish Abuse,Marijuana Abuse,,,,,,C0018614,D002189,,,,
+BMGC_DS01025,BMG_DS001319,70369002;21719001,Hay fever,,CA08.00,Allergic rhinitis due to pollen,J30.1,,,C0018621,,MTHU037792,MONDO:0005324,seasonal allergic rhinitis,Seasonal allergic rhinitis | Seasonal allergic rhinitis (disorder) | Pollinosis | Hay fever | Hayfever | Allergic rhinitis caused by pollens | Allergic rhinitis caused by pollen | Allergic rhinitis caused by pollen (disorder)
+BMGC_DS01026,BMG_DS001320,,,,,,,DOID:11934,head and neck cancer,C0018671,,,MONDO:0005586,head and neck neoplasm,
+BMGC_DS01027,BMG_DS001321,,"Hearing Loss, Bilateral","Hearing Loss, Bilateral",,,,,,C0018775,D006312,,,,
+BMGC_DS01028,BMG_DS001323,44057004;155255001,Conductive hearing loss,,,,,,,C0018777,,MTHU036345,MONDO:0020679,conductive hearing loss disorder,Conductive hearing loss | Conductive deafness | CHL - Conductive hearing loss | CD - Conductive deafness | Conductive hearing loss (disorder) | Conductive hearing loss | Conductive hearing loss (disorder)
+BMGC_DS01029,BMG_DS001324,,"Hearing Loss, High-Frequency","Hearing Loss, High-Frequency",,,,,,C0018780,D006316,,,,
+BMGC_DS01030,BMG_DS001325,,,,,,,,,C0018781,,,MONDO:0013098,noise induced hearing loss,
+BMGC_DS01031,BMG_DS001326,,,,,,,DOID:10003,sensorineural hearing loss,C0018784,,,MONDO:0020678,sensorineural hearing loss disorder,
+BMGC_DS01032,BMG_DS001327,,Heart Aneurysm,Heart Aneurysm,,,,DOID:9768,heart aneurysm,C0018789,D006322,,MONDO:0006779,heart aneurysm,
+BMGC_DS01033,BMG_DS001328,,Cardiac Arrest,Heart Arrest,,,,DOID:0060319,cardiac arrest,C0018790,D006323,,MONDO:0000745,cardiac arrest,
+BMGC_DS01034,BMG_DS001329,,Heart Block,Heart Block,,,,,,C0018794,D006327,,,,
+BMGC_DS01035,BMG_DS001330,,,,,,,DOID:1682,congenital heart disease,C0018798,,,,,
+BMGC_DS01036,BMG_DS001331,,Heart Diseases,Heart Diseases,,,,DOID:114,heart disease,C0018799,D006331,,MONDO:0005267,heart disorder,
+BMGC_DS01037,BMG_DS001332,84114007;155374007,Heart failure,,,,I50,DOID:6000,congestive heart failure,C0018801,,MTHU009472,MONDO:0005252,heart failure,Heart failure | Myocardial failure | Weak heart | Cardiac failure | Heart failure (disorder) | HF - Heart failure | Cardiac insufficiency | Heart failure | Heart failure (disorder)
+BMGC_DS01038,BMG_DS001333,195108009;42343007,Congestive heart failure,,,,,DOID:6000,congestive heart failure,C0018802,,MTHU005753,MONDO:0005009,congestive heart failure,Heart failure: [right] or [congestive] | Biventricular failure | Right heart failure | Right ventricular failure | Congestive cardiac failure | Congestive heart failure | Heart failure: [right] or [congestive] (disorder) | Congestive heart failure | Congestive heart disease | Congestive cardiac failure | CCF - Congestive cardiac failure | CHF - Congestive heart failure | Congestive heart failure (disorder)
+BMGC_DS01039,BMG_DS001334,,,,,,,DOID:117,heart cancer,C0018809,,,MONDO:0021209,heart neoplasm,
+BMGC_DS01040,BMG_DS001336,,"Heart Rupture, Post-Infarction","Heart Rupture, Post-Infarction",,,,,,C0018814,D006342,,,,
+BMGC_DS01041,BMG_DS001337,,,,,,,DOID:1681,heart septal defect,C0018816,,,MONDO:0002078,heart septal defect,
+BMGC_DS01042,BMG_DS001338,,,,,,,DOID:1882,atrial heart septal defect,C0018817,,,MONDO:0006664,atrial septal defect,
+BMGC_DS01043,BMG_DS001339,,,,,,,DOID:1657,ventricular septal defect,C0018818,,,MONDO:0002070,ventricular septal defect,
+BMGC_DS01044,BMG_DS001340,368009,Heart valve disease,,,,,DOID:4079,heart valve disease,C0018824,,,MONDO:0002869,heart valve disorder,Heart valve disorder | Valvular heart disease | Heart valve disease | Disorder of heart valve | Heart valve disorder (disorder)
+BMGC_DS01045,BMG_DS001342,,,,,,,DOID:0060125,heavy chain disease,C0018852,,,MONDO:0019464,heavy chain disease,
+BMGC_DS01046,BMG_DS001343,,,,,,,DOID:0060125,heavy chain disease,C0018854,,,MONDO:0015046,gamma-heavy chain disease,
+BMGC_DS01047,BMG_DS001345,187518006;27601005,Helminthiasis,Helminthiasis,,,,DOID:883,parasitic helminthiasis infectious disease,C0018889,D006373,,MONDO:0004664,helminthiasis,Helminthiasis | Helminthiasis (disorder) | Helminth infection | Helminthiasis | Helminthosis | Worms | Worm infestation | Worm infection | Infection caused by Cestoda and/or Trematoda and/or Phylum Nemata | Infection caused by Cestoda and/or Trematoda and/or Phylum Nematoda (disorder) | Infection caused by Cestoda and/or Trematoda and/or Phylum Nematoda
+BMGC_DS01048,BMG_DS001346,,"Helminthiasis, Animal","Helminthiasis, Animal",,,,,,C0018891,D006374,,MONDO:0025082,"helminthiasis, animal",
+BMGC_DS01049,BMG_DS001348,,,,,,,DOID:255,hemangioma,C0018916,,,MONDO:0006500,hemangioma,
+BMGC_DS01050,BMG_DS001349,,,,,,,DOID:483,cavernous hemangioma,C0018920,,,MONDO:0003155,cavernous hemangioma,
+BMGC_DS01051,BMG_DS001350,,,,,,,DOID:264,hemangiopericytoma,C0018922,,,MONDO:0005094,hemangiopericytoma,
+BMGC_DS01052,BMG_DS001351,,,,,,,DOID:0001816,angiosarcoma,C0018923,,,MONDO:0016982,angiosarcoma,
+BMGC_DS01053,BMG_DS001352,,,,,,,DOID:801,hemarthrosis,C0018924,,,MONDO:0004431,hemarthrosis,
+BMGC_DS01054,BMG_DS001354,66259004,Hematocele of tunica vaginalis testis,,,,,DOID:12332,hematocele of tunica vaginalis testis,C0018931,,,MONDO:0001495,hematocele of tunica vaginalis testis,Male hematocele | Hematocele of tunica vaginalis testis | Hematocele | Haematocoele of tunica vaginalis testis | Haematocoele | Male haematocele | Male hematocele (disorder)
+BMGC_DS01055,BMG_DS001355,405729008;72256005,Hematochezia,Gastrointestinal Hemorrhage,,,,,,C0018932,D006471,MTHU006474,,,Hematochezia (finding) | Haematochezia | Hematochezia | Bloody stool | Bright red blood in stool | Bright red blood per rectum | Passage of bloody stools | BRBPR - Bright red blood per rectum | Feces: blood | Blood in feces | Faeces: blood | Blood in faeces | Blood in stool | Fresh blood passed per rectum | Passage of bloody stools | Blood in stool | Blood in faeces | Faeces: blood | Blood in feces | Feces: blood | Blood in stool (disorder)
+BMGC_DS01056,BMG_DS001357,,Hematological Disease,Hematologic Diseases,,,,DOID:74,hematopoietic system disease,C0018939,D006402,,MONDO:0005570,hematologic disorder,
+BMGC_DS01057,BMG_DS001358,,,,,,,DOID:9958,hemometra,C0018948,,,MONDO:0006782,hemometra,
+BMGC_DS01058,BMG_DS001359,39134007,Hematomyelia,Spinal Cord Vascular Diseases,,,G95.19,,,C0018949,D020758,,,,Hematomyelia | Haematomyelia | Hematomyelia (disorder) | Intramedullary haemorrhage | Intramedullary hemorrhage
+BMGC_DS01059,BMG_DS001361,197937006;266568001;34436003,Hematuria,Hematuria,,,R31,,,C0018965,D006417,MTHU036916,,,Hematuria (& [traumatic] or [essential]) | Essential hematuria | Hematuria | Traumatic hematuria | Traumatic haematuria | Haematuria | Essential haematuria | Haematuria (& [traumatic] or [essential]) | Haematuria (& [traumatic] or [essential]) (disorder) | Haematuria | Hematuria | Haematuria (disorder) | Hematuria | Haematuria | Blood in urine | Blood in urine (finding)
+BMGC_DS01060,BMG_DS001362,75390007;399323001;65194006,Hemeralopia,Vision Disorders,,,H53.11,,,C0018975,D014786,MTHU038321,,,Day blindness | Hemeralopia | Difficulty seeing at night | Night blindness | Nyctalopia | Day blindness (disorder) | Day blindness (disorder) | Day blindness | Hemeralopia | Night blindness | Nyctalopia | Night blindness (disorder) | Difficulty seeing at night
+BMGC_DS01061,BMG_DS001365,,,,,,,,,C0018991,,,MONDO:0001170,hemiplegia,
+BMGC_DS01062,BMG_DS001366,,Biliary Tract Hemorrhage,Hemobilia,,,,,,C0018994,D006431,,,,
+BMGC_DS01063,BMG_DS001367,86781004;267504005;154751003;399187006,Hemochromatosis,Hemochromatosis,,,E83.11,DOID:2352,hemochromatosis,C0018995,D006432,,,,"Hemochromatosis | Bronzed cirrhosis | Pigmentary cirrhosis of liver | von Recklinghausen-Appelbaum disease | Iron storage disease | Familial hemochromatosis | Hereditary hemochromatosis | Primary hemochromatosis | Idiopathic hemochromatosis | Familial haemochromatosis | Hereditary haemochromatosis | Idiopathic haemochromatosis | Primary haemochromatosis | Bronzed diabetes | von Recklinghausen-Applebaum disease | Haemochromatosis | Hemochromatosis (disorder) | Hemochromatosis | Iron &/or copper &/or magnesium disorder (& [haemochromatosis] or [Wilson's disease]) | Haemochromatosis | Copper disorder | Magnesium disorder | Iron disorder | Iron, copper, magnesium metabolism disorder | Iron, copper, magnesium disord | Wilson's disease | Iron &/or copper &/or magnesium disorder (& [hemochromatosis] or [Wilson's disease]) | Iron &/or copper &/or magnesium disorder (& [haemochromatosis] or [Wilson's disease]) (disorder) | Haemochromatosis | Hemochromatosis | Iron &/or copper &/or magnesium disorder (& [haemochromatosis] or [Wilson's disease]) | Iron disorder | Iron, copper, magnesium disord | Magnesium disorder | Wilson's disease | Iron, copper, magnesium metabolism disorder | Copper disorder | Iron &/or copper &/or magnesium disorder (& [hemochromatosis] or [Wilson's disease]) | Iron &/or copper &/or magnesium disorder (& [haemochromatosis] or [Wilson's disease]) (disorder) | Hemochromatosis (disorder) | Hemochromatosis | Iron storage disease | Haemochromatosis"
+BMGC_DS01064,BMG_DS001368,,Hemoglobin C Disease,Hemoglobin C Disease,,,,DOID:2859,hemoglobin C disease,C0019021,D006445,,MONDO:0016242,hemoglobin C disease,
+BMGC_DS01065,BMG_DS001369,,Hemoglobin F Disease,beta-Thalassemia,,,,,,C0019025,D017086,,MONDO:0020989,hereditary persistence of fetal hemoglobin,
+BMGC_DS01066,BMG_DS001370,,Hemoglobin SC Disease,Hemoglobin SC Disease,,,,DOID:10923,sickle cell anemia,C0019034,D006450,,MONDO:0016669,sickle cell-hemoglobin c disease syndrome,
+BMGC_DS01067,BMG_DS001371,,Hemoglobinopathies,Hemoglobinopathies,,,,DOID:2860,hemoglobinopathy,C0019045,D006453,,MONDO:0019050;MONDO:0044348,inherited hemoglobinopathy | hemoglobinopathy,
+BMGC_DS01068,BMG_DS001372,,,,,,,DOID:582,hemoglobinuria,C0019048,,,MONDO:0003656,hemoglobinuria,
+BMGC_DS01069,BMG_DS001374,,"Hemoglobinuria, Paroxysmal","Hemoglobinuria, Paroxysmal",,,,DOID:0060284,paroxysmal nocturnal hemoglobinuria,C0019050,D006457,,,,
+BMGC_DS01070,BMG_DS001375,,Hemolytic-Uremic Syndrome,Hemolytic-Uremic Syndrome,,,,DOID:12554,hemolytic-uremic syndrome,C0019061,D006463,,MONDO:0001549,hemolytic-uremic syndrome,
+BMGC_DS01071,BMG_DS001376,,,,,,,DOID:11482,hemopericardium,C0019064,,,MONDO:0005783,hemopericardium,
+BMGC_DS01072,BMG_DS001377,,Reactive Hemophagocytic Syndrome,"Lymphohistiocytosis, Hemophagocytic",,,,,,C0019068,D051359,,,,
+BMGC_DS01073,BMG_DS001378,28293008,Hemophilia A,Hemophilia A,,,D66,DOID:12134,factor VIII deficiency,C0019069,D006467,134500;306700,MONDO:0010602,hemophilia A,Hemophilia A | Hereditary factor VIII deficiency disease | Classical hemophilia | AHG deficiency disease | Sex-linked factor VIII deficiency | Congenital factor VIII deficiency disease | Haemophilia A | Classical haemophilia | Hereditary factor VIII deficiency disease (disorder)
+BMGC_DS01074,BMG_DS001379,16632002,Hemopneumothorax,Hemopneumothorax,CB26,Haemothorax,J94.2,DOID:2718,hemopneumothorax,C0019077,D006468,MTHU038542,MONDO:0006783,hemopneumothorax,Hemopneumothorax | Pneumohaemothorax | Pneumohemothorax | Haemopneumothorax | Hemopneumothorax (disorder)
+BMGC_DS01075,BMG_DS001380,,Hemorrhagic Disorders,Hemorrhagic Disorders,,,,DOID:2213,hemorrhagic disease,C0019087,D006474,,MONDO:0002243,hemorrhagic disease,
+BMGC_DS01076,BMG_DS001381,,Hemorrhagic Disease of Newborn,Vitamin K Deficiency Bleeding,,,,,,C0019088,D006475,,MONDO:0006784,hemorrhagic disease of newborn,
+BMGC_DS01077,BMG_DS001384,,"Hemorrhagic Fever, Crimean","Hemorrhagic Fever, Crimean",,,,DOID:12287,Crimean-Congo hemorrhagic fever,C0019099,D006479,,MONDO:0020501,Crimean-Congo hemorrhagic fever,
+BMGC_DS01078,BMG_DS001385,,Severe Dengue,Severe Dengue,,,,DOID:12206,dengue hemorrhagic fever,C0019100,D019595,,MONDO:0005358,Dengue hemorrhagic fever,
+BMGC_DS01079,BMG_DS001386,,Hemorrhagic Fever with Renal Syndrome,Hemorrhagic Fever with Renal Syndrome,,,,DOID:11266,Hantavirus hemorrhagic fever with renal syndrome,C0019101,D006480,,MONDO:0018081,hemorrhagic fever-renal syndrome,
+BMGC_DS01080,BMG_DS001387,,"Hemorrhagic Fever, Omsk","Hemorrhagic Fever, Omsk",,,,DOID:992,Omsk hemorrhagic fever,C0019103,D006481,,MONDO:0017882,Omsk hemorrhagic fever,
+BMGC_DS01081,BMG_DS001389,70153002,Hemorrhoids,Hemorrhoids,,,,DOID:9746,hemorrhoid,C0019112,D006484,,MONDO:0004872,hemorrhoid,Hemorrhoids | Piles | Haemorrhoids | Haemorrhoid | Piles - haemorrhoids | Hemorrhoid | Piles - hemorrhoids | Hemorrhoids (disorder)
+BMGC_DS01082,BMG_DS001390,39011001,Hemosiderosis,Hemosiderosis,,,,DOID:12119,hemosiderosis,C0019114,D006486,MTHU067796,MONDO:0001436,hemosiderosis,Hemosiderosis | Haemosiderosis | Hemosiderosis (disorder)
+BMGC_DS01083,BMG_DS001392,,Hepatic Coma,Hepatic Encephalopathy,,,,DOID:12550,hepatic coma,C0019147,D006501,,MONDO:0001548,hepatic coma,
+BMGC_DS01084,BMG_DS001393,,Hepatic Encephalopathy,Hepatic Encephalopathy,,,,DOID:13413,hepatic encephalopathy,C0019151,D006501,,MONDO:0001711,hepatic encephalopathy,
+BMGC_DS01085,BMG_DS001394,,Hepatic Vein Thrombosis,Budd-Chiari Syndrome,,,,DOID:11512,Budd-Chiari syndrome,C0019154,D006502,,MONDO:0006786,hepatic vein thrombosis,
+BMGC_DS01086,BMG_DS001395,,Hepatic Veno-Occlusive Disease,Hepatic Veno-Occlusive Disease,,,,DOID:0080177,hepatic veno-occlusive disease,C0019156,D006504,,MONDO:0019514,hepatic veno-occlusive disease,
+BMGC_DS01087,BMG_DS001396,128241005;29001004,Hepatitis,Hepatitis,,,,,,C0019158,D006505,MTHU067436,MONDO:0002251,hepatitis,Inflammatory disorder of liver | Inflammatory disease of liver | Hepatitis | Inflammatory liver disease | Inflammatory disease of liver (disorder) | Hepatitis | Hepatitis (disorder)
+BMGC_DS01088,BMG_DS001397,40468003,Hepatitis A,Hepatitis A,,,,DOID:12549,hepatitis A,C0019159,D006506,,MONDO:0005790,hepatitis A virus infection,"Viral hepatitis, type A | Infectious hepatitis | Hepatitis A | IH - Infectious hepatitis | Viral hepatitis, type A (disorder)"
+BMGC_DS01089,BMG_DS001398,66071002,Hepatitis B,Hepatitis B,,,,DOID:2043,hepatitis B,C0019163,D006509,,MONDO:0005344,hepatitis B virus infection,Type B viral hepatitis | Serum hepatitis | Hepatitis B | SH - Serum hepatitis | Hepatitis B infection | Viral hepatitis type B | Viral hepatitis type B (disorder)
+BMGC_DS01090,BMG_DS001399,,"Hepatitis, Alcoholic","Hepatitis, Alcoholic",,,,,,C0019187,D006519,,MONDO:0001505,alcoholic hepatitis,
+BMGC_DS01091,BMG_DS001400,,"Hepatitis, Animal","Hepatitis, Animal",,,,,,C0019188,D006520,,MONDO:0024945,"hepatitis, non-human animal",
+BMGC_DS01092,BMG_DS001401,,"Hepatitis, Chronic","Hepatitis, Chronic",,,,DOID:2237,hepatitis,C0019189,D006521,,,,
+BMGC_DS01093,BMG_DS001403,,"Hepatitis, Viral, Animal","Hepatitis, Viral, Animal",,,,DOID:1884,viral hepatitis,C0019194,D006524,,MONDO:0025085,"hepatitis, viral, animal",
+BMGC_DS01094,BMG_DS001404,,"Hepatitis, Viral, Human","Hepatitis, Viral, Human",,,,,,C0019195,D006525,,,,
+BMGC_DS01095,BMG_DS001405,186643004;50711007;154349000,Hepatitis C,Hepatitis C,,,,DOID:1883,hepatitis C,C0019196,D006526,,MONDO:0005231,hepatitis C virus infection,Hepatitis C | Hepatitis C (disorder) | Viral hepatitis C | Type C viral hepatitis | Hepatitis C | Viral hepatitis type C | Viral hepatitis type C (disorder)
+BMGC_DS01096,BMG_DS001406,,Hepatolenticular Degeneration,Hepatolenticular Degeneration,,,,DOID:893,Wilson disease,C0019202,D006527,277900,MONDO:0010200,Wilson disease,
+BMGC_DS01097,BMG_DS001407,,Hepatorenal Syndrome,Hepatorenal Syndrome,,,,DOID:11823,hepatorenal syndrome,C0019212,D006530,,MONDO:0001382,hepatorenal syndrome,
+BMGC_DS01098,BMG_DS001408,,"Angioedemas, Hereditary","Angioedemas, Hereditary",,,,DOID:14735,hereditary angioedema,C0019243,D054179,,MONDO:0019623,hereditary angioedema,
+BMGC_DS01099,BMG_DS001409,,Hereditary Diseases,"Genetic Diseases, Inborn",,,,DOID:630,genetic disease,C0019247,D030342,,MONDO:0003847,hereditary disease,
+BMGC_DS01100,BMG_DS001411,,,,,,,DOID:3763,hermaphroditism,C0019269,,,,,
+BMGC_DS01101,BMG_DS001412,,,,,,,DOID:3827,congenital diaphragmatic hernia,C0019284,,,,,
+BMGC_DS01102,BMG_DS001413,,,,,,,DOID:0060320,inguinal hernia,C0019294,,,,,
+BMGC_DS01103,BMG_DS001414,,"Inguinal Hernia, Direct","Hernia, Inguinal",,,,DOID:0060320,inguinal hernia,C0019295,D006552,,MONDO:0000746, | obsolete inguinal hernia,
+BMGC_DS01104,BMG_DS001415,,,,,,,DOID:0060320,inguinal hernia,C0019296,,,,,
+BMGC_DS01105,BMG_DS001418,,,,,,,DOID:9976,heroin dependence,C0019337,,,MONDO:0005367,heroin dependence,
+BMGC_DS01106,BMG_DS001419,186659004;37428001;154358007;266197009,Herpangina,Herpangina,1F05.1,Enteroviral vesicular pharyngitis,B08.5,DOID:10883,herpangina,C0019338,D006557,,MONDO:0005791,herpangina,Herpangina | Enteroviral vesicular pharyngitis | Herpangina (disorder) | Enteroviral vesicular pharyngitis | Enteroviral vesicular pharyngitis (disorder) | (Other coxsackie disease) or (herpangina) | Other coxsackie disease | Herpangina | (Other coxsackie disease) or (herpangina) (disorder) | (Other coxsackie disease) or (herpangina) | Herpangina | Other coxsackie disease | (Other coxsackie disease) or (herpangina) (disorder)
+BMGC_DS01107,BMG_DS001420,,Genital Herpes,Herpes Genitalis,,,,DOID:8704,genital herpes,C0019342,D006558,,MONDO:0005770,genital herpes,
+BMGC_DS01108,BMG_DS001422,,Herpes Labialis,Herpes Labialis,,,,,,C0019345,D006560,,MONDO:0043653,herpes labialis,
+BMGC_DS01109,BMG_DS001423,88594005,Herpes simplex infection,,,,,DOID:8566,herpes simplex,C0019348,,,MONDO:0004609,herpes simplex infectious disease,Herpes simplex | Herpes simplex infection | Herpes simplex viral infection | Herpes simplex (disorder) | Herpes simplex complex
+BMGC_DS01110,BMG_DS001424,,"Keratitis, Herpetic","Keratitis, Herpetic",,,,,,C0019357,D016849,,MONDO:0015288,herpes simplex virus keratitis,
+BMGC_DS01111,BMG_DS001426,4740000,Herpes zoster (disorder),,,,,DOID:8536,herpes zoster,C0019360,,,MONDO:0005609,herpes zoster,Herpes zoster | Shingles | Zona | Herpes zoster infection | Herpes zoster (disorder) | Zoster
+BMGC_DS01112,BMG_DS001428,,Herpes Zoster Ophthalmicus,Herpes Zoster Ophthalmicus,,,,,,C0019364,D006563,,MONDO:0005883,ophthalmic herpes zoster,
+BMGC_DS01113,BMG_DS001429,4740000,Herpes zoster without mention of complication,,,,,,,C0019366,,,,,Herpes zoster | Shingles | Zona | Herpes zoster infection | Herpes zoster (disorder) | Zoster
+BMGC_DS01114,BMG_DS001430,,Herpesviridae Infections,Herpesviridae Infections,,,,,,C0019372,D006566,,MONDO:0005794,Herpesviridae infectious disease,
+BMGC_DS01115,BMG_DS001433,,"Deficiency, Hexosediphosphatase","Fructose-1,6-Diphosphatase Deficiency",,,,,,C0019489,D015319,,,,
+BMGC_DS01116,BMG_DS001434,,,,,,,DOID:3896,hidradenoma,C0019522,,,MONDO:0021110,sweat gland adenoma,
+BMGC_DS01117,BMG_DS001435,,High Pressure Neurological Syndrome,High Pressure Neurological Syndrome,,,,DOID:3230,high pressure neurological syndrome,C0019537,D006610,,MONDO:0002570,high pressure neurological syndrome,
+BMGC_DS01118,BMG_DS001438,,,,,,,DOID:14175,von Hippel-Lindau disease,C0019562,,193300,MONDO:0008667,von Hippel-Lindau disease,
+BMGC_DS01119,BMG_DS001439,,Hirschsprung Disease,Hirschsprung Disease,,,,DOID:10487,Hirschsprung's disease,C0019569,D006627,,MONDO:0018309,Hirschsprung disease,
+BMGC_DS01120,BMG_DS001441,40090008;399939002,Hirsutism,Hirsutism,ED72.Z,"Hirsutism, unspecified",L68.0,,,C0019572,D006628,MTHU036369,,,Hirsuties | Pilosis | Excessive growth of hair | Hairiness | Hirsutes | Excessive hair growth | Excessive hair growth (disorder) | Hirsutism (disorder) | Hirsutism | Hirsuties | Pilosis | Hirsutes
+BMGC_DS01121,BMG_DS001442,64351000;266225001;154423006,Leech infestation,,,,,DOID:11079,leech infestation,C0019575,,,MONDO:0001191,hirudiniasis,Leech infestation | Hirudiniasis | Leeches | Hirudiniasis - leech infestation | Leech infestation (disorder) | (Other infectious & parasitic disease) or (infestation: [leech] or [maggot]) or (myiasis) or (toxoplasmosis) | Myiasis | Toxoplasmosis | Other infectious and parasitic diseases | Maggot infestation | Leech infestation | Other infect. and parasit.dis. | (Other infectious & parasitic disease) or (infestation: [leech] or [maggot]) or (myiasis) or (toxoplasmosis) (disorder) | Maggot infestation | Myiasis | Toxoplasmosis | Leech infestation | Other infectious and parasitic diseases | Other infect. and parasit.dis. | (Other infectious & parasitic disease) or (infestation: [leech] or [maggot]) or (myiasis) or (toxoplasmosis) | (Other infectious & parasitic disease) or (infestation: [leech] or [maggot]) or (myiasis) or (toxoplasmosis) (disorder)
+BMGC_DS01122,BMG_DS001443,,,,,,,DOID:2570,malignant histiocytic disease,C0019613,,,,,
+BMGC_DS01123,BMG_DS001444,,,,,,,DOID:3405,histiocytosis,C0019618,,,MONDO:0002637,histiocytosis,
+BMGC_DS01124,BMG_DS001445,,,,,,,DOID:2571,Langerhans-cell histiocytosis,C0019621,,604856,MONDO:0018310,Langerhans cell histiocytosis,
+BMGC_DS01125,BMG_DS001447,,"Histiocytosis, Non-Langerhans-Cell","Histiocytosis, Non-Langerhans-Cell",,,,DOID:4330,non-Langerhans-cell histiocytosis,C0019624,D015616,,MONDO:0015531,non-Langerhans cell histiocytosis,
+BMGC_DS01126,BMG_DS001448,,,,,,,,,C0019625,,,MONDO:0006412,sinus histiocytosis with massive lymphadenopathy,
+BMGC_DS01127,BMG_DS001449,35047007,Histomoniasis,Protozoan Infections,,,,,,C0019640,D011528,,MONDO:0002428,protozoa infectious disease,Infection by Histomonas | Histomoniasis | Histomonosis | Infection caused by Histomonas | Infection caused by Histomonas (disorder)
+BMGC_DS01128,BMG_DS001450,154408001;266218008;12962009,Histoplasmosis,Histoplasmosis,,,B39,DOID:1731,histoplasmosis,C0019655,D006660,,MONDO:0018312,histoplasmosis,Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) | Aspergillosis | Mycoses - other | Histoplasmosis | Other mycoses | Piedra | Sporotrichosis | Coccidioidomycosis | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) (disorder) | Coccidioidomycosis | Other mycoses | Sporotrichosis | Mycoses - other | Piedra | Histoplasmosis | Aspergillosis | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) (disorder) | Histoplasmosis | Histoplasmosis (disorder)
+BMGC_DS01129,BMG_DS001451,,,,,,,DOID:334,histrionic personality disorder,C0019681,,,MONDO:0002613,histrionic personality disorder,
+BMGC_DS01130,BMG_DS001452,,HIV Infections,HIV Infections,,,,DOID:526,human immunodeficiency virus infectious disease,C0019693,D015658,,MONDO:0005109,HIV infectious disease,
+BMGC_DS01131,BMG_DS001453,,"Hereditary, Type VII, Motor and Sensory Neuropathy",Hereditary Sensory and Motor Neuropathy,,,,,,C0019816,D015417,,,,
+BMGC_DS01132,BMG_DS001454,,,,,,,DOID:8567,Hodgkin's lymphoma,C0019829,,236000,MONDO:0009348,classic Hodgkin lymphoma,
+BMGC_DS01133,BMG_DS001456,190709008;11282001,Homocystinuria,Homocystinuria,,,E72.11,DOID:9263,homocystinuria,C0019880,D006712,MTHU037510,MONDO:0004737,homocystinuria,Homocystinuria | Homocystinuria (disorder)
+BMGC_DS01134,BMG_DS001457,,Hookworm Infections,Hookworm Infections,,,,,,C0019911,D006725,,,,
+BMGC_DS01135,BMG_DS001458,397513003;193912000;267736000;155172004;74612003,Hordeolum,Hordeolum,,,,DOID:9909,hordeolum,C0019917,D006726,,MONDO:0005800,hordeolum,Hordeolum (disorder) | Hordeolum | Stye | Sty | Boil of eyelid | Hordeolum externum | Hordeolum | Furuncle of eyelid | Stye (disorder) | (Stye &/or [hordeolum]) or (cellulitis eyelid) or (meibomian cyst) | Cellulitis - eyelid | Cellulitis of eyelid | Meibomian cyst | Stye | Hordeolum | Stye/hordeolum | (Stye &/or [hordeolum]) or (cellulitis eyelid) or (meibomian cyst) (disorder) | (Stye &/or [hordeolum]) or (cellulitis eyelid) or (meibomian cyst) | Hordeolum | Stye | Meibomian cyst | Cellulitis - eyelid | Stye/hordeolum | Cellulitis of eyelid | (Stye &/or [hordeolum]) or (cellulitis eyelid) or (meibomian cyst) (disorder) | Hordeolum | Hordeolum (disorder)
+BMGC_DS01136,BMG_DS001460,1489008;193912000,Hordeolum externum,,,,H00.01,DOID:13134,hordeolum externum,C0019919,,,MONDO:0001642,hordeolum externum,"Hordeolum externum | Hordeolum externum (disorder) | External hordeolum | Stye | Boil of eyelid | Sty | Furuncle of eyelid | Hordeolum, external | Stye | Sty | Boil of eyelid | Hordeolum externum | Hordeolum | Furuncle of eyelid | Stye (disorder)"
+BMGC_DS01137,BMG_DS001461,,Horner Syndrome,Horner Syndrome,,,,DOID:11486,Horner's syndrome,C0019937,D006732,,MONDO:0001294,Horner syndrome,
+BMGC_DS01138,BMG_DS001462,,Horse Diseases,Horse Diseases,,,,,,C0019940,D006734,,MONDO:0024950,horse disease,
+BMGC_DS01139,BMG_DS001463,,"Hereditary Sensory Autonomic Neuropathy, Type 1",Hereditary Sensory and Autonomic Neuropathies,,,,DOID:0050548;DOID:0070162,hereditary sensory and autonomic neuropathy type 1 | hereditary sensory neuropathy,C0020071,D009477,,MONDO:0018213,hereditary sensory and autonomic neuropathy type 1,
+BMGC_DS01140,BMG_DS001464,,"Hereditary Sensory Autonomic Neuropathy, Type 2",Hereditary Sensory and Autonomic Neuropathies,,,,DOID:0050548;DOID:0070161,hereditary sensory neuropathy | hereditary sensory and autonomic neuropathy type 2,C0020072,D009477,,,,
+BMGC_DS01141,BMG_DS001465,,HSAN Type IV,Hereditary Sensory and Autonomic Neuropathies,,,,DOID:0050548;DOID:0070146,hereditary sensory neuropathy type 4 | hereditary sensory neuropathy,C0020074,D009477,256800,MONDO:0009746,hereditary sensory and autonomic neuropathy type 4,
+BMGC_DS01142,BMG_DS001466,,"Hereditary Sensory Autonomic Neuropathy, Type 5",Hereditary Sensory and Autonomic Neuropathies,,,,DOID:0050548;DOID:0070145,hereditary sensory neuropathy | hereditary sensory and autonomic neuropathy type 5,C0020075,D009477,608654,MONDO:0012092,hereditary sensory and autonomic neuropathy type 5,
+BMGC_DS01143,BMG_DS001468,,HTLV-I Infections,HTLV-I Infections,,,,,,C0020097,D015490,,MONDO:0005801,human T-lymphotropic virus 1 infectious disease,
+BMGC_DS01144,BMG_DS001470,,Huntington Disease,Huntington Disease,,,,DOID:12858,Huntington's disease,C0020179,D006816,143100,MONDO:0007739,Huntington disease,
+BMGC_DS01145,BMG_DS001471,,Hyaline Membrane Disease,Hyaline Membrane Disease,,,,DOID:12716,newborn respiratory distress syndrome,C0020192,D006819,,,,
+BMGC_DS01146,BMG_DS001472,,,,,,,DOID:3590,gestational trophoblastic neoplasm,C0020217,,,MONDO:0006248,hydatidiform mole,
+BMGC_DS01147,BMG_DS001473,,,,,,,DOID:8488,polyhydramnios,C0020224,,,MONDO:0004585,polyhydramnios,
+BMGC_DS01148,BMG_DS001474,,,,,,,DOID:4626,hydranencephaly,C0020225,,,MONDO:0016344,hydranencephaly,
+BMGC_DS01149,BMG_DS001475,,Hydroa Vacciniforme,Hydroa Vacciniforme,,,,,,C0020241,D006837,,MONDO:0018024,hydroa vacciniforme,
+BMGC_DS01150,BMG_DS001476,230745008;154997008;154995000;192807008;267687006,Hydrocephalus,Hydrocephalus,,,G91,DOID:10908,hydrocephalus,C0020255,D006849,MTHU002499,MONDO:0001150,hydrocephalus,Hydrocephalus | Hydrocephalus (disorder) | Hydrocephaly | Hydrocephalus | Hydrocephalus (disorder) | Child cerebral degeneration | Senile brain degen. | Hydrocephalus | Senile degeneration of brain | (Child cerebral degeneration) or (hydrocephalus) or (senile brain degeneration) | (Child cerebral degeneration) or (hydrocephalus) or (senile brain degeneration) (disorder) | Hydrocephalus | Senile brain degen. | Senile degeneration of brain | Child cerebral degeneration | (Child cerebral degeneration) or (hydrocephalus) or (senile brain degeneration) | (Child cerebral degeneration) or (hydrocephalus) or (senile brain degeneration) (disorder)
+BMGC_DS01151,BMG_DS001477,,,,,,,,,C0020256,,,MONDO:0016349,congenital hydrocephalus,
+BMGC_DS01152,BMG_DS001478,,"Hydrocephalus, Normal Pressure","Hydrocephalus, Normal Pressure",,,,DOID:1572,normal pressure hydrocephalus,C0020258,D006850,236690,MONDO:0009366,normal pressure hydrocephalus,
+BMGC_DS01153,BMG_DS001479,155866001;43064006,Hydronephrosis,Hydronephrosis,,,,DOID:11111,hydronephrosis,C0020295,D006869,MTHU001611,MONDO:0005510,hydronephrosis,Hydronephrosis | Hydronephrosis (disorder)
+BMGC_DS01154,BMG_DS001480,,,,,,,DOID:11212,hydrophthalmos,C0020302,,,MONDO:0020366,congenital glaucoma,
+BMGC_DS01155,BMG_DS001481,,Hydrops Fetalis,Hydrops Fetalis,,,,,,C0020305,D015160,,MONDO:0015193,hydrops fetalis,
+BMGC_DS01156,BMG_DS001482,266407006;155608000;79231000,Hydrothorax,Hydrothorax,CB2Z,"Pleural, diaphragm or mediastinal disorders, unspecified",J94.8,,,C0020312,D006876,MTHU037917,,,(Pleural effusion NOS) or (haemothorax) or (hydrothorax) | Hemothorax | Hydrothorax | Pleural effusion NOS | Haemothorax | (Pleural effusion NOS) or (hemothorax) or (hydrothorax) | (Pleural effusion NOS) or (haemothorax) or (hydrothorax) (disorder) | (Pleural effusion NOS) or (hemothorax) or (hydrothorax) | Pleural effusion NOS | Hydrothorax | (Pleural effusion NOS) or (haemothorax) or (hydrothorax) | Hemothorax | Haemothorax | (Pleural effusion NOS) or (haemothorax) or (hydrothorax) (disorder) | Hydrothorax | Pleural effusion with transudate | Hydrothorax (disorder)
+BMGC_DS01157,BMG_DS001483,187153007;44917000,Hymenolepiasis,Hymenolepiasis,1F74,Hymenolepiasis,B71.0,DOID:10074,hymenolepiasis,C0020413,D006925,,MONDO:0005802,hymenolepiasis,Dwarf tapeworm infection | Hymenolepiasis | Rat tapeworm infection | Hymenolepiasis (& [dwarf] or [rat]) | Hymenolepiasis (& [dwarf] or [rat]) (disorder) | Hymenolepiasis | Hymenolepiosis | Hymenolepiasis (disorder)
+BMGC_DS01158,BMG_DS001484,88213004;154709005;190506003;267484005,Hyperaldosteronism,Hyperaldosteronism,,,E26,DOID:446,primary hyperaldosteronism,C0020428,D006929,MTHU038571,MONDO:0003009,hyperaldosteronism,Aldosteronism | Hyperaldosteronism | Aldosteronism (disorder) | Adrenal disorders: [other] or [Conn's syndrome] or [hyperaldosteronism] or [Waterhouse-Friderichen] | Conn's syndrome | Hyperaldosteronism | Waterhouse-Friderichen | Other adrenal disorders | Adrenal disorders: [other] or [Conn's syndrome] or [hyperaldosteronism] or [Waterhouse-Friderichen] (disorder) | Hyperaldosteronism (& [Bartter's syndrome] or [Conn's syndrome]) | Aldosteronism | Hyperaldosteronism | Bartter's syndrome | Conn's syndrome | Hyperaldosteronism (& [Bartter's syndrome] or [Conn's syndrome]) (disorder) | Adrenal disorders: [other] or [Conn's syndrome] or [hyperaldosteronism] or [Waterhouse-Friderichen] | Conn's syndrome | Other adrenal disorders | Hyperaldosteronism | Waterhouse-Friderichen | Adrenal disorders: [other] or [Conn's syndrome] or [hyperaldosteronism] or [Waterhouse-Friderichen] (disorder)
+BMGC_DS01159,BMG_DS001485,235904007;267509000;14783006;154770008,Hyperbilirubinemia,Hyperbilirubinemia,,,,DOID:2741,bilirubin metabolic disorder,C0020433,D006932,,,,Hyperbilirubinemia | Hyperbilirubinaemia | Hyperbilirubinemia (disorder) | Hyperbilirubinemia | Hyperbilirubinaemia (& [Gilbert's syndrome]) | Gilbert's syndrome | Hyperbilirubinaemia | Hyperbilirubinemia (& [Gilbert's syndrome]) | Hyperbilirubinaemia (& [Gilbert's syndrome]) (disorder) | Hyperbilirubinemia | Hyperbilirubinaemia | Bilirubinemia | Bilirubinaemia | Hyperbilirubinemia (disorder) | Gilbert's syndrome | Hyperbilirubinemia (& [Gilbert's syndrome]) | Hyperbilirubinaemia (& [Gilbert's syndrome]) | Hyperbilirubinaemia | Hyperbilirubinemia | Hyperbilirubinaemia (& [Gilbert's syndrome]) (disorder)
+BMGC_DS01160,BMG_DS001486,,"Hyperbilirubinemia, Hereditary","Hyperbilirubinemia, Hereditary",,,,DOID:2741,bilirubin metabolic disorder,C0020435,D006933,,MONDO:0002408,hereditary hyperbilirubinemia,
+BMGC_DS01161,BMG_DS001487,66931009;267505006;154752005,Hypercalcemia,Hypercalcemia,,,E83.52,DOID:12678,hypercalcemia,C0020437,D006934,,MONDO:0001566,hypercalcemia disease,"Hypercalcemia | Hypercalcemia syndrome | Hypercalcaemia syndrome | Hypercalcaemia | Hypercalcemia (disorder) | (Phosphorus &/or calcium disorders (& [hypercalcemia] or [hypercalcinuria] or [hypocalcemia]) or (nephrocalcinosis) | Nephrocalcinosis | Calcium disorder | Phosphorus, calcium disorders | Hypercalcinuria | Phosphorus and calcium disorders | Phosphorus disorder | Hypocalcaemia | Hypercalcaemia | (Phosphorus &/or calcium disorders (& [hypercalcaemia] or [hypercalcinuria] or [hypocalcaemia]) or (nephrocalcinosis) | Hypercalcemia | Hypocalcemia | (Phosphorus &/or calcium disorders (& [hypercalcaemia] or [hypercalcinuria] or [hypocalcaemia]) or (nephrocalcinosis) (disorder) | (Phosphorus &/or calcium disorders (& [hypercalcemia] or [hypercalcinuria] or [hypocalcemia]) or (nephrocalcinosis) | Nephrocalcinosis | Phosphorus and calcium disorders | Phosphorus, calcium disorders | Hypercalcinuria | Phosphorus disorder | Calcium disorder | (Phosphorus &/or calcium disorders (& [hypercalcaemia] or [hypercalcinuria] or [hypocalcaemia]) or (nephrocalcinosis) | Hypercalcemia | Hypocalcemia | Hypocalcaemia | Hypercalcaemia | (Phosphorus &/or calcium disorders (& [hypercalcaemia] or [hypercalcinuria] or [hypocalcaemia]) or (nephrocalcinosis) (disorder)"
+BMGC_DS01162,BMG_DS001488,78537008,Hypercementosis,Hypercementosis,DA07.5,Cementum dysplasia,K03.4,DOID:12733,hypercementosis,C0020441,D006936,,MONDO:0006790,hypercementosis,Hypercementosis | Cementation hyperplasia | Cementum hyperplasia | Cementosis | Hypercementosis (disorder)
+BMGC_DS01163,BMG_DS001489,13644009;154740003;267500001,Hypercholesterolemia,Hypercholesterolemia,,,,,,C0020443,D006937,MTHU030735,,,Hypercholesterolemia | Hypercholesterolaemia | Hypercholesterolemia (disorder) | High cholesterol | Cholesterolaemia-famil. | Congenital xanthoma | Xanthoma - congenital | (Hypercholesterolemia: [pure] or [familial]) or (xanthoma - congenital) | (Hypercholesterolaemia: [pure] or [familial]) or (xanthoma - congenital) | Pure hypercholesterolaemia | Hypercholesterolaemia | Hypercholesterolemia | Pure hypercholesterolemia | (Hypercholesterolaemia: [pure] or [familial]) or (xanthoma - congenital) (disorder) | Congenital xanthoma | Cholesterolaemia-famil. | Xanthoma - congenital | Hypercholesterolaemia | Pure hypercholesterolaemia | Hypercholesterolemia | Pure hypercholesterolemia | (Hypercholesterolaemia: [pure] or [familial]) or (xanthoma - congenital) | (Hypercholesterolemia: [pure] or [familial]) or (xanthoma - congenital) | (Hypercholesterolaemia: [pure] or [familial]) or (xanthoma - congenital) (disorder)
+BMGC_DS01164,BMG_DS001490,,"Hypercholesterolemia, Familial",Hyperlipoproteinemia Type II,,,,DOID:13810,familial hypercholesterolemia,C0020445,D006938,,MONDO:0005439,familial hypercholesterolemia,
+BMGC_DS01165,BMG_DS001491,,,,,,,,,C0020450,,,MONDO:0006791,hyperemesis gravidarum,
+BMGC_DS01166,BMG_DS001493,30098003;247441003,Hyperemia,Hyperemia,,,,,,C0020452,D006940,MTHU054354,,,Hyperemia | Vascular engorgement | Local congestion | Engorgement | Hyperaemia | Hyperemia (morphologic abnormality) | Erythema | Erythema (finding) | Erythema - observation
+BMGC_DS01167,BMG_DS001495,154840005;127388009;191396003;267571003,Hypergammaglobulinemia,Hypergammaglobulinemia,,,,,,C0020455,D006942,MTHU032383,,,(Other blood diseases) or (familial erythrocytosis) or (hypergammaglobulinemia) | Erythrocytosis - familial | Other blood diseases | Familial erythrocytosis | (Other blood diseases) or (familial erythrocytosis) or (hypergammaglobulinaemia) | Hypergammaglobulinaemia | Hypergammaglobulinemia | (Other blood diseases) or (familial erythrocytosis) or (hypergammaglobulinaemia) (disorder) | Hypergammaglobulinemia | Hypergammaglobulinaemia | Hypergammaglobulinemia (finding) | Hypergammaglobulinaemia | Hypergammaglobulinemia | Hypergammaglobulinemia (finding) | (Other blood diseases) or (familial erythrocytosis) or (hypergammaglobulinemia) | Familial erythrocytosis | Other blood diseases | Erythrocytosis - familial | Hypergammaglobulinaemia | (Other blood diseases) or (familial erythrocytosis) or (hypergammaglobulinaemia) | Hypergammaglobulinemia | (Other blood diseases) or (familial erythrocytosis) or (hypergammaglobulinaemia) (disorder)
+BMGC_DS01168,BMG_DS001496,154719004;80394007;144187006;270004003,Hyperglycemia,Hyperglycemia,,,,DOID:4195,hyperglycemia,C0020456,D006943,MTHU002042,MONDO:0002909,hyperglycemia,Hyperglycaemia | Hyperglycemia | Hyperglycaemia (disorder) | Hyperglycemia | Hyperglycaemia | Hyperglycemia (disorder) | Sugar result - blood | Blood sugar result | Plasma glucose level | Glucose result - blood | Blood glucose result | (Blood sugar result [& glucose]) or (plasma glucose level) or (hyperglycemia) | (Blood sugar result [& glucose]) or (plasma glucose level) or (hyperglycaemia) | Hyperglycemia | Hyperglycaemia | (Blood sugar result [& glucose]) or (plasma glucose level) or (hyperglycaemia) (procedure) | (Blood sugar result [& glucose]) or (plasma glucose level) or (hyperglycemia) | Blood glucose result | Sugar result - blood | Glucose result - blood | Blood sugar result | Plasma glucose level | Hyperglycaemia | (Blood sugar result [& glucose]) or (plasma glucose level) or (hyperglycaemia) | Hyperglycemia | (Blood sugar result [& glucose]) or (plasma glucose level) or (hyperglycaemia) (procedure)
+BMGC_DS01169,BMG_DS001497,,Hyperglycemic Hyperosmolar Nonketotic Coma,Hyperglycemic Hyperosmolar Nonketotic Coma,,,,,,C0020457,D006944,,,,
+BMGC_DS01170,BMG_DS001498,154694003;267477002;83469008,Hyperinsulinism,Hyperinsulinism,,,,DOID:2018,hyperinsulinism,C0020459,D006946,,MONDO:0002177,hyperinsulinism,Hyperinsulinism | Zollinger - Ellison syndrome | Zollinger-Ellison syndrome | Other pancreatic secretion dis | Zollinger-Ellison syndr | (Other pancreatic secretion disorder) or (hyperinsulinism) or (Zollinger-Ellison syndrome) | (Other pancreatic secretion disorder) or (hyperinsulinism) or (Zollinger-Ellison syndrome) (disorder) | Zollinger-Ellison syndr | Zollinger-Ellison syndrome | Other pancreatic secretion dis | Hyperinsulinism | Zollinger - Ellison syndrome | (Other pancreatic secretion disorder) or (hyperinsulinism) or (Zollinger-Ellison syndrome) | (Other pancreatic secretion disorder) or (hyperinsulinism) or (Zollinger-Ellison syndrome) (disorder) | Hyperinsulinism | Hyperinsulinism (disorder) | Hyperinsulinaemia | Hyperinsulinemia
+BMGC_DS01171,BMG_DS001499,154739000;267499005;55822004,Hyperlipidemia,Hyperlipidemias,,,,DOID:1168,familial hyperlipidemia,C0020473,D006949,MTHU002043,MONDO:0021187,hyperlipidemia,Hyperlipidemia | Hyperlipidaemia | Disorders of lipid metabolism (& [Fredrickson types] or [hyperlipidaemia]) | Disorders of lipid metabolism (& [Fredrickson types] or [hyperlipidemia]) | Fredrickson types | Disorders of lipid metabolism | Lipid metabol. disorder | Disorder of lipid metabolism | Disorders of lipid metabolism (& [Fredrickson types] or [hyperlipidaemia]) (disorder) | Disorders of lipid metabolism (& [Fredrickson types] or [hyperlipidemia]) | Disorders of lipid metabolism (& [Fredrickson types] or [hyperlipidaemia]) | Hyperlipidemia | Hyperlipidaemia | Fredrickson types | Disorder of lipid metabolism | Disorders of lipid metabolism | Lipid metabol. disorder | Disorders of lipid metabolism (& [Fredrickson types] or [hyperlipidaemia]) (disorder) | Hyperlipidemia | Lipidemia | HLD - Hyperlipidemia | HLD - Hyperlipidaemia | Hyperlipidaemia | Lipidaemia | Hyperlipidemia (disorder)
+BMGC_DS01172,BMG_DS001500,,"Hyperlipidemia, Familial Combined","Hyperlipidemia, Familial Combined",,,,DOID:13809,familial combined hyperlipidemia,C0020474,D006950,144250,MONDO:0001807;MONDO:0007759,"obsolete familial combined hyperlipidemia | hyperlipidemia, familial combined, LPL related",
+BMGC_DS01173,BMG_DS001501,,Hyperlipoproteinemias,Hyperlipoproteinemias,,,,DOID:1168,familial hyperlipidemia,C0020476,D006951,,MONDO:0037748,hyperlipoproteinemia,
+BMGC_DS01174,BMG_DS001502,,Hyperlipoproteinemia Type III,Hyperlipoproteinemia Type III,,,,DOID:3145,hyperlipoproteinemia type III,C0020479,D006952,617347,MONDO:0018473,hyperlipoproteinemia type 3,
+BMGC_DS01175,BMG_DS001503,,Hyperlipoproteinemia Type IV,Hyperlipoproteinemia Type IV,,,,DOID:1172,hyperlipoproteinemia type IV,C0020480,D006953,144600,MONDO:0007761,obsolete hyperlipoproteinemia type IV,
+BMGC_DS01176,BMG_DS001504,,Hyperlipoproteinemia Type V,Hyperlipoproteinemia Type V,,,,DOID:1171,hyperlipoproteinemia type V,C0020481,D006954,144650,MONDO:0007762,hyperlipoproteinemia type V,
+BMGC_DS01177,BMG_DS001505,39355002;771115008;190879002,Hypernatremia,Hypernatremia,,,,,,C0020488,D006955,MTHU007803,,,Hypernatremia | Na overload | Na excess | Sodium retention | Hypernatraemia | Hypernatremia (disorder) | Sodium overload | Sodium overload | Hypernatremia | Na excess | Na overload | Hypernatraemia | Hypernatremia (disorder) | Hyperosmolality &/or hypernatremia | Hypernatraemia | Hyperosmolality and or hypernatraemia | Hypernatremia | Hyperosmolality and or hypernatremia | Hyperosmolality &/or hypernatraemia | Hyperosmolality &/or hypernatraemia (disorder)
+BMGC_DS01178,BMG_DS001506,38101003,Hyperopia,Hyperopia,,,,DOID:9834,hyperopia,C0020490,D006956,MTHU036505,MONDO:0004891,hyperopia,Hypermetropia | Hyperopia | Farsightedness | Hypermetropia (disorder) | Longsightedness | Longsighted
+BMGC_DS01179,BMG_DS001507,13814009,Hyperostosis,Hyperostosis,,,,DOID:205,hyperostosis,C0020492,D015576,MTHU036636,MONDO:0002185,hyperostosis,Hypertrophy of bone | Bony overgrowth | Hyperostosis | Hypertrophy of bone (morphologic abnormality)
+BMGC_DS01180,BMG_DS001509,12138000;788954009;17401000119104,Hyperostosis of skull,,FB80.3,Hyperostosis of skull,M85.2,DOID:0060756;DOID:0060757,sclerosteosis 1 | sclerosteosis 2,C0020496,,,,,Skull enlargement | Large skull | Large head | Large head (disorder) | Hyperostosis of skull (finding) | Hyperostosis of skull | Hyperostosis of skull (disorder) | Hyperostosis of skull
+BMGC_DS01181,BMG_DS001510,,Cortical Congenital Hyperostosis,"Hyperostosis, Cortical, Congenital",,,,DOID:4257,Caffey disease,C0020497,D006958,114000,MONDO:0007244,Caffey disease,
+BMGC_DS01182,BMG_DS001511,,"Hyperostosis, Diffuse Idiopathic Skeletal","Hyperostosis, Diffuse Idiopathic Skeletal",,,,DOID:6652,diffuse idiopathic skeletal hyperostosis,C0020498,D004057,,MONDO:0007127,diffuse idiopathic skeletal hyperostosis,
+BMGC_DS01183,BMG_DS001513,367621000119107,Hyperoxaluria,Hyperoxaluria,,,R82.992,DOID:2977,primary hyperoxaluria,C0020500,D006959,MTHU037859,,,Hyperoxaluria | Hyperoxaluria (disorder)
+BMGC_DS01184,BMG_DS001514,,Primary Hyperoxaluria,"Hyperoxaluria, Primary",,,,DOID:2977,primary hyperoxaluria,C0020501,D006960,,MONDO:0002474,primary hyperoxaluria,
+BMGC_DS01185,BMG_DS001515,154696001;66999008;190451000,Hyperparathyroidism,Hyperparathyroidism,,,,DOID:13543,hyperparathyroidism,C0020502,D006961,MTHU036868,MONDO:0001741,hyperparathyroidism,Hyperparathyroidism | Hyperparathyroidism (disorder) | Hyperparathyroidism | HPTH - Hyperparathyroidism | Hyperparathyroidism (disorder) | Hyperparathyroidism (& [osteitis fibrosa cystica] or [Von Recklinghausen's bone disease]) | Osteitis fibrosa cystica | Von Recklinghausen's bone disease | Hyperparathyroidism | Hyperparathyroidism (& [osteitis fibrosa cystica] or [Von Recklinghausen's bone disease]) (disorder)
+BMGC_DS01186,BMG_DS001516,,"Hyperparathyroidism, Secondary","Hyperparathyroidism, Secondary",,,,DOID:12466,secondary hyperparathyroidism,C0020503,D006962,,MONDO:0006964,secondary hyperparathyroidism,
+BMGC_DS01187,BMG_DS001517,10649000,Hyperpituitarism,Hyperpituitarism,,,,DOID:2444,hyperpituitarism,C0020506,D006964,,MONDO:0006793,hyperpituitarism,Hyperpituitarism | Pituitary hyperfunction | Anterior pituitary hyperfunction | Hyperpituitarism (disorder) | Pituitary hyperfunction (ant.)
+BMGC_DS01188,BMG_DS001518,,,,,,,,,C0020507,,,MONDO:0005043,hyperplasia,
+BMGC_DS01189,BMG_DS001519,190468001;237662005;21170004,Hyperprolactinemia,Hyperprolactinemia,5A60.1,Hyperprolactinaemia,E22.1,DOID:12700,hyperprolactinemia,C0020514,D006966,MTHU037102,MONDO:0005804,hyperprolactinemia,Hyperprolactinemia | Hyperprolactinaemia | Hyperprolactinaemia (disorder) | Hyperprolactinemia | Hyperprolactinaemia | Hyperprolactinemia (disorder) | Idiopathic hyperprolactinemia | Idiopathic hyperprolactinaemia | Idiopathic hyperprolactinemia (disorder)
+BMGC_DS01190,BMG_DS001520,,,,,,,DOID:1205,allergic disease,C0020517,,,MONDO:0005271,allergic disease,
+BMGC_DS01191,BMG_DS001521,,,,,,,,,C0020522,,,MONDO:0002459,type IV hypersensitivity disease,
+BMGC_DS01192,BMG_DS001522,,Hypersomnia with Periodic Respiration,Sleep Apnea Syndromes,,,,,,C0020529,D012891,,,,
+BMGC_DS01193,BMG_DS001523,267570002;58381000;154839008,Hypersplenism,Hypersplenism,3B81.B,Hypersplenism,D73.1,DOID:6376,hypersplenism,C0020532,D006971,MTHU037461,MONDO:0006795,hypersplenism,Diseases of spleen (& [hypersplenism] or [infarct]) | Spleen disease | Hypersplenism | Splenic infarct | Diseases of spleen | Diseases of spleen (& [hypersplenism] or [infarct]) (disorder) | Hypersplenism | Dyssplenism | Big spleen syndrome | Hypersplenia | Hypersplenism (disorder) | Diseases of spleen (& [hypersplenism] or [infarct]) | Hypersplenism | Spleen disease | Diseases of spleen | Splenic infarct | Diseases of spleen (& [hypersplenism] or [infarct]) (disorder)
+BMGC_DS01194,BMG_DS001524,155295004;38341003;266287006;194756002,Hypertensive disease,,,,,DOID:10763,hypertension,C0020538,,,MONDO:0005044,hypertensive disorder,"(Hypertensive disease) or (hypertension) | Hypertensive disease | Hypertension | (Hypertensive disease) or (hypertension) (disorder) | High blood pressure | Hypertensive vascular disease | Hypertensive vascular degeneration | Hypertension | BP - High blood pressure | Systemic arterial hypertension | HBP - High blood pressure | HT - Hypertension | High blood pressure disorder | BP+ - Hypertension | Hypertensive disorder, systemic arterial (disorder) | Hypertensive disorder | HTN - Hypertension | Hypertensive disorder, systemic arterial | (Hypertensive disease) or (hypertension) | Hypertension | Hypertensive disease | (Hypertensive disease) or (hypertension) (disorder) | Hypertensive disease | Hypertensive disease (disorder)"
+BMGC_DS01195,BMG_DS001525,,Malignant Hypertension,"Hypertension, Malignant",,,,DOID:10824,malignant hypertension,C0020540,D006974,,MONDO:0006846,malignant hypertension,
+BMGC_DS01196,BMG_DS001526,,Portal Hypertension,"Hypertension, Portal",,,,DOID:10762,portal hypertension,C0020541,D006975,,MONDO:0005080,portal hypertension,
+BMGC_DS01197,BMG_DS001527,,,,,,,DOID:6432,pulmonary hypertension,C0020542,,,MONDO:0005149,pulmonary hypertension,
+BMGC_DS01198,BMG_DS001528,194775007;28119000,Renal hypertension,,,,,DOID:1073,renal hypertension,C0020544,,,MONDO:0001105,renal hypertension,(Renal hypertension) or (hypertensive renal disease NOS) | Hypertensive renal disease NOS | Renal hypertension | (Renal hypertension) or (hypertensive renal disease NOS) (disorder) | Renal hypertension | Renal hypertension (disorder)
+BMGC_DS01199,BMG_DS001529,,"Hypertension, Renovascular","Hypertension, Renovascular",,,,DOID:1591,renovascular hypertension,C0020545,D006978,,MONDO:0006947,renovascular hypertension,
+BMGC_DS01200,BMG_DS001530,34486009;267464006;154655004;190239004,Hyperthyroidism,Hyperthyroidism,,,,DOID:7998,hyperthyroidism,C0020550,D006980,MTHU001214,MONDO:0004425,hyperthyroidism,"Hyperthyroidism | Hyperthyroidism (disorder) | Goiter - toxic | Thyrotoxicosis +/- goiter | Toxic goiter | Thyrotoxicosis: [+/- goitre] or [toxic goitre] or [Graves disease] or [thyroid nodule] | Toxic goitre | Goitre - toxic | Thyrotoxicosis +/- goitre | Toxic thyroid nodule | Thyrotoxicosis | Hyperthyroidism | Graves' disease | Nodule - thyroid, toxic | Graves disease | Thyrotoxicosis: [+/- goiter] or [toxic goiter] or [Graves disease] or [thyroid nodule] | Thyrotoxicosis: [+/- goitre] or [toxic goitre] or [Graves disease] or [thyroid nodule] (disorder) | Thyrotoxicosis: [+/- goitre] or [toxic goitre] or [Graves disease] or [thyroid nodule] | Thyrotoxicosis: [+/- goiter] or [toxic goiter] or [Graves disease] or [thyroid nodule] | Hyperthyroidism | Graves' disease | Nodule - thyroid, toxic | Graves disease | Thyrotoxicosis | Toxic thyroid nodule | Toxic goitre | Thyrotoxicosis +/- goitre | Goitre - toxic | Goiter - toxic | Thyrotoxicosis +/- goiter | Toxic goiter | Thyrotoxicosis: [+/- goitre] or [toxic goitre] or [Graves disease] or [thyroid nodule] (disorder) | Toxic goiter | Toxic goitre | ([Thyrotoxicosis] or [hyperthyroidism]) or (toxic goitre) | ([Thyrotoxicosis] or [hyperthyroidism]) or (toxic goiter) | Hyperthyroidism | Thyrotoxicosis | ([Thyrotoxicosis] or [hyperthyroidism]) or (toxic goitre) (disorder)"
+BMGC_DS01201,BMG_DS001531,,Hyperthyroxinemia,Hyperthyroxinemia,,,,DOID:2855,hyperthyroxinemia,C0020551,D006981,,MONDO:0005333,hyperthyroxinemia,
+BMGC_DS01202,BMG_DS001532,156409007;201164001;29966009,Hypertrichosis,Hypertrichosis,,,L68,DOID:420,hypertrichosis,C0020555,D006983,MTHU036754,MONDO:0019280,hypertrichosis,Hypertrichosis | Hypertrichosis (disorder) | Hypertrichosis | Excessive hairiness | Polytrichia | Hypertrichiasis | Polytrichosis | Hirsutism - hypertrichosis | Hypertrichosis (disorder)
+BMGC_DS01203,BMG_DS001533,302870006,Hypertriglyceridemia,Hypertriglyceridemia,,,,,,C0020557,D015228,,,,Hypertriglyceridaemia | Hypertriglyceridemia | Hypertriglyceridemia (disorder)
+BMGC_DS01204,BMG_DS001534,35863000;198353000,Hypertrophic elongation of cervix,,,,,DOID:2251,hypertrophic elongation of cervix,C0020561,,,MONDO:0002255,hypertrophic elongation of cervix,Hypertrophic elongation of cervix | Hypertrophic elongation of cervix (disorder)
+BMGC_DS01205,BMG_DS001535,,,,,,,DOID:10688,hypertrophy of breast,C0020565,,,MONDO:0001100,hypertrophy of breast,
+BMGC_DS01206,BMG_DS001536,40608009,Hypertropia,Strabismus,9C80.2,Vertical or torsional strabismus,H50.2,DOID:9837,hypertropia,C0020575,D013285,MTHU037273,MONDO:0004893,hypertropia,Hypertropia | Hypertropia (disorder)
+BMGC_DS01207,BMG_DS001537,64559002,Hypervitaminosis A,Hypervitaminosis A,5B90.0,Hypervitaminosis A,E67.0,DOID:9972,hypervitaminosis A,C0020579,D006986,,MONDO:0006798,hypervitaminosis A,Hypervitaminosis A | Hypervitaminosis A (disorder)
+BMGC_DS01208,BMG_DS001539,,,,,,,DOID:13868,hypoactive sexual desire disorder,C0020594,,,MONDO:0001821,hypoactive sexual desire disorder,
+BMGC_DS01209,BMG_DS001540,60086000,Hypoaldosteronism,Hypoaldosteronism,,,E27.40,,,C0020595,D006994,MTHU041707,,,Aldosterone deficiency | Aldosterone deficiency (disorder) | Hypoaldosteronism
+BMGC_DS01210,BMG_DS001541,,Hypobetalipoproteinemias,Hypobetalipoproteinemias,,,,DOID:1390,hypobetalipoproteinemia,C0020597,D006995,,MONDO:0017774,hypobetalipoproteinemia,
+BMGC_DS01211,BMG_DS001542,267505006;154752005;5291005,Hypocalcemia,Hypocalcemia,,,E83.51,,,C0020598,D006996,MTHU036379,,,"(Phosphorus &/or calcium disorders (& [hypercalcemia] or [hypercalcinuria] or [hypocalcemia]) or (nephrocalcinosis) | Nephrocalcinosis | Calcium disorder | Phosphorus, calcium disorders | Hypercalcinuria | Phosphorus and calcium disorders | Phosphorus disorder | Hypocalcaemia | Hypercalcaemia | (Phosphorus &/or calcium disorders (& [hypercalcaemia] or [hypercalcinuria] or [hypocalcaemia]) or (nephrocalcinosis) | Hypercalcemia | Hypocalcemia | (Phosphorus &/or calcium disorders (& [hypercalcaemia] or [hypercalcinuria] or [hypocalcaemia]) or (nephrocalcinosis) (disorder) | (Phosphorus &/or calcium disorders (& [hypercalcemia] or [hypercalcinuria] or [hypocalcemia]) or (nephrocalcinosis) | Nephrocalcinosis | Phosphorus and calcium disorders | Phosphorus, calcium disorders | Hypercalcinuria | Phosphorus disorder | Calcium disorder | (Phosphorus &/or calcium disorders (& [hypercalcaemia] or [hypercalcinuria] or [hypocalcaemia]) or (nephrocalcinosis) | Hypercalcemia | Hypocalcemia | Hypocalcaemia | Hypercalcaemia | (Phosphorus &/or calcium disorders (& [hypercalcaemia] or [hypercalcinuria] or [hypocalcaemia]) or (nephrocalcinosis) (disorder) | Hypocalcemia | Hypocalcemia syndrome | Calcium deficiency disease | Hypocalcaemia syndrome | Hypocalcaemia | Hypocalcemia (disorder)"
+BMGC_DS01212,BMG_DS001543,86353007,Hypocalciuria,,,,,,,C0020599,,MTHU017734,,,Hypocalciuria | Hypocalciuria (disorder)
+BMGC_DS01213,BMG_DS001544,,,,,,,DOID:12883,hypochondriasis,C0020604,,,MONDO:0001596,hypochondriasis,
+BMGC_DS01214,BMG_DS001545,,Hypodermyiasis,Hypodermyiasis,,,,DOID:12926,hypodermyiasis,C0020607,D007000,,MONDO:0005805,hypodermyiasis,
+BMGC_DS01215,BMG_DS001546,,,,,,,,,C0020608,,,MONDO:0005486,tooth agenesis,
+BMGC_DS01216,BMG_DS001547,199004,Hypogalactia,Lactation Disorders,JB46.4,Hypogalactia,O92.4,,,C0020610,D007775,,,,Decreased lactation | Hypogalactia | Hypolactation | Insufficient lactation | Poor lactation | Inadequate lactation | Decreased lactation (finding)
+BMGC_DS01217,BMG_DS001548,302866003;154691006;66694000,Hypoglycemia,Hypoglycemia,,,,DOID:9993,hypoglycemia,C0020615,D007003,MTHU000371,MONDO:0004946,hypoglycemia,Hypoglycaemia | Hypoglycemia | Hypoglycemia (disorder) | Hypoglycaemia | Hypoglycemia | Hypoglycaemia (disorder) | Hypoglycemia | Hypoglycaemia | Hypoglycemia (disorder)
+BMGC_DS01218,BMG_DS001549,267384006;154692004;71898001;190428000;267476006,Hypoglycemic coma,,,,,DOID:1607,hypoglycemic coma,C0020617,,,,,Hypoglycaemic coma | Hypoglycemic coma | Coma due to hypoglycaemia | Coma due to hypoglycemia (disorder) | Coma due to hypoglycemia | Insulin coma | Coma - insulin | Hypoglycemic coma (& [insulin]) | Hypoglycaemic coma (& [insulin]) | Hypoglycaemic coma | Hypoglycemic coma | Hypoglycaemic coma (& [insulin]) (disorder) | Hypoglycemic coma | Hypoglycaemic coma | Hypoglycemic coma (disorder) | Coma: [hypoglycemic] or [insulin] | Insulin coma | Hypoglycemic coma | Hypoglycaemic coma | Coma: [hypoglycaemic] or [insulin] | Coma: [hypoglycaemic] or [insulin] (disorder) | Insulin coma | Coma - insulin | Hypoglycaemic coma | Hypoglycemic coma | Hypoglycaemic coma (& [insulin]) | Hypoglycemic coma (& [insulin]) | Hypoglycaemic coma (& [insulin]) (disorder)
+BMGC_DS01219,BMG_DS001550,48130008,Hypogonadism,Hypogonadism,,,,DOID:1924,hypogonadism,C0020619,D007006,MTHU000132,MONDO:0002146,hypogonadism,Hypogonadism | Hypogonadism (disorder)
+BMGC_DS01220,BMG_DS001551,45004005;201189007,Hypohidrosis,Hypohidrosis,EE01.Z,"Hypohidrosis, unspecified",L74.4,DOID:11155,hypohidrosis,C0020620,D007007,MTHU036385,MONDO:0006560,obsolete hypohidrosis,Hypohidrosis | Oligohidrosis | Hypohidrosis (disorder) | Hypohydrosis | (Anhidrosis) or (hypohidrosis) or (oligohidrosis) | Oligohidrosis | Hypohidrosis | Anhidrosis | (Anhidrosis) or (hypohidrosis) or (oligohidrosis) (disorder)
+BMGC_DS01221,BMG_DS001552,,,,,,,DOID:1387,hypolipoproteinemia,C0020623,,,MONDO:0001822,hypolipoproteinemia,
+BMGC_DS01222,BMG_DS001553,266669004;64206003;156041006,Hypomenorrhea,Menstruation Disturbances,,,,,,C0020624,D008599,,,,(Hypomenorrhea) or (scanty periods) | Scanty periods | Hypomenorrhoea | (Hypomenorrhoea) or (scanty periods) | Hypomenorrhea | (Hypomenorrhoea) or (scanty periods) (disorder) | Hypomenorrhea | Hypomenorrhoea | Hypomenorrhea (finding) | Spotting only at periods | Scanty period | Light menstrual period | Scanty periods | Scanty periods | (Hypomenorrhea) or (scanty periods) | (Hypomenorrhoea) or (scanty periods) | Hypomenorrhea | Hypomenorrhoea | (Hypomenorrhoea) or (scanty periods) (finding)
+BMGC_DS01223,BMG_DS001554,267507003;154756008;89627008;190880004,Hyponatremia,Hyponatremia,,,,,,C0020625,D007010,MTHU000164,,,(Sodium deficiency) or (hyponatremia) | Sodium deficiency | Hyponatraemia | Hyponatremia | (Sodium deficiency) or (hyponatraemia) | (Sodium deficiency) or (hyponatraemia) (disorder) | (Sodium deficiency) or (hyponatremia) | Sodium deficiency | (Sodium deficiency) or (hyponatraemia) | Hyponatraemia | Hyponatremia | (Sodium deficiency) or (hyponatraemia) (disorder) | Hyponatremia | Hyponatraemia | Hyponatremia (finding) | Hyposmolality &/or hyponatraemia | Hypo-osmolality and or hyponatremia | Hyponatremia | Hyposmolality and or hyponatremia | Hyposmolality and or hyponatraemia | Hyponatraemia | Hypo-osmolality and or hyponatraemia | Hyposmolality &/or hyponatremia | Hyposmolality &/or hyponatraemia (disorder)
+BMGC_DS01224,BMG_DS001555,154697005;267479004;36976004,Hypoparathyroidism,Hypoparathyroidism,,,E20,DOID:11199,hypoparathyroidism,C0020626,D007011,MTHU006713,MONDO:0001220,hypoparathyroidism,(Hypoparathyroidism) or (pseudo-hypoparathyroidism) or (tetany) | Pseudo-hypoparathyroidism | Hypoparathyroidism | Tetany | (Hypoparathyroidism) or (pseudo-hypoparathyroidism) or (tetany) (disorder) | Hypoparathyroidism | Pseudo-hypoparathyroidism | Tetany | (Hypoparathyroidism) or (pseudo-hypoparathyroidism) or (tetany) | (Hypoparathyroidism) or (pseudo-hypoparathyroidism) or (tetany) (disorder) | Hypoparathyroidism | Deficiency of parathyroid hormone | Deficiency of parathyrin | Hypoparathyroidism (disorder) | Deficiency of PTH (parathyroid hormone)
+BMGC_DS01225,BMG_DS001557,70848009;190859005,Hypophosphatasia,Hypophosphatasia,,,E83.39,DOID:14213,hypophosphatasia,C0020630,D007014,,MONDO:0018570,hypophosphatasia,Hypophosphatasia | Hypophosphatasia (disorder) | Hypophosphatasia | Alkaline phosphatase deficiency | Hypophosphatasia (disorder)
+BMGC_DS01226,BMG_DS001559,74728003,Hypopituitarism,Hypopituitarism,5A61.0,Hypopituitarism,E23.0,DOID:0090072;DOID:0090087;DOID:0060875;DOID:0090073;DOID:0090076;DOID:0090092;DOID:0060873;DOID:0090080;DOID:0090075;DOID:0090077;DOID:0090071;DOID:0090082;DOID:0090084;DOID:0090074;DOID:9406;DOID:0090093;DOID:0060874;DOID:0090078;DOID:0090070;DOID:0090085;DOID:0090094;DOID:0090086;DOID:0090083;DOID:0090081;DOID:0090079;DOID:0090089;DOID:0090090,hypogonadotropic hypogonadism 5 with or without anosmia | hypogonadotropic hypogonadism 7 with or without anosmia | hypogonadotropic hypogonadism 9 with or without anosmia | isolated growth hormone deficiency type IB | hypogonadotropic hypogonadism 21 with or without anosmia | hypogonadotropic hypogonadism 17 with or without anosmia | hypogonadotropic hypogonadism 6 with or without anosmia | isolated growth hormone deficiency type IA | isolated growth hormone deficiency type III | hypopituitarism | hypogonadotropic hypogonadism 10 with or without anosmia | hypogonadotropic hypogonadism 2 with or without anosmia | hypogonadotropic hypogonadism 22 with or without anosmia | hypogonadotropic hypogonadism 4 with or without anosmia | hypogonadotropic hypogonadism 1 with or without anosmia | hypogonadotropic hypogonadism 15 with or without anosmia | hypogonadotropic hypogonadism 16 with or without anosmia | hypogonadotropic hypogonadism 3 with or without anosmia | hypogonadotropic hypogonadism 14 with or without anosmia | hypogonadotropic hypogonadism 13 with or without anosmia | hypogonadotropic hypogonadism 19 with or without anosmia | hypogonadotropic hypogonadism 18 with or without anosmia | hypogonadotropic hypogonadism 12 with or without anosmia | hypogonadotropic hypogonadism | hypogonadotropic hypogonadism 11 with or without anosmia | hypogonadotropic hypogonadism 8 with or without anosmia | hypogonadotropic hypogonadism 20 with or without anosmia,C0020635,D007018,MTHU036880,MONDO:0005152,hypopituitarism,Hypopituitarism | Deficient secretion of one OR more pituitary hormones | Pituitary insufficiency | Pituitary deficiency | Pituitary failure | Hypopituitarism (disorder) | Pituitary hypofunction
+BMGC_DS01227,BMG_DS001560,154750002;267503004;8900005,Hypoproteinemia,Hypoproteinemia,,,,,,C0020639,D007019,MTHU001376,,,(Plasma protein metabolism disorder: & [hyperproteinemia] or [hypoproteinemia]) or (Waldenstrom's macroglobulinemia) | Plasma protein metab. disorder | Waldenstrom's macroglob'naemia | (Plasma protein metabolism disorder: & [hyperproteinaemia] or [hypoproteinaemia]) or (Waldenstrom's macroglobulinaemia) | Hyperproteinemia | Waldenstrom's macroglobulinemia | Hypoproteinemia | Hyperproteinaemia | Hypoproteinaemia | Waldenstrom's macroglobulinaemia | (Plasma protein metabolism disorder: & [hyperproteinaemia] or [hypoproteinaemia]) or (Waldenstrom's macroglobulinaemia) (disorder) | (Plasma protein metabolism disorder: & [hyperproteinemia] or [hypoproteinemia]) or (Waldenstrom's macroglobulinemia) | Plasma protein metab. disorder | Waldenstrom's macroglob'naemia | Hypoproteinaemia | Hyperproteinaemia | Waldenstrom's macroglobulinaemia | (Plasma protein metabolism disorder: & [hyperproteinaemia] or [hypoproteinaemia]) or (Waldenstrom's macroglobulinaemia) | Hyperproteinemia | Hypoproteinemia | Waldenstrom's macroglobulinemia | (Plasma protein metabolism disorder: & [hyperproteinaemia] or [hypoproteinaemia]) or (Waldenstrom's macroglobulinaemia) (disorder) | Hypoproteinemia | Hypoproteinaemia | Hypoproteinemia (disorder)
+BMGC_DS01228,BMG_DS001561,87807004,Hypopyon,,,,H20.05,DOID:10443,hypopyon,C0020641,,,MONDO:0001036,hypopyon,Hypopyon | Hypopyon (disorder) | Pus in anterior chamber
+BMGC_DS01229,BMG_DS001562,,,,,,,,,C0020649,,,MONDO:0005468,hypotensive disorder,
+BMGC_DS01230,BMG_DS001563,,"Hypotension, Orthostatic","Hypotension, Orthostatic",,,,,,C0020651,D007024,,MONDO:0005469,orthostatic hypotension,
+BMGC_DS01231,BMG_DS001564,,Hypothalamic Diseases,Hypothalamic Diseases,,,,DOID:1931,hypothalamic disease,C0020655,D007027,,MONDO:0002150,hypothalamic disorder,
+BMGC_DS01232,BMG_DS001565,,,,,,,DOID:3644,hypothalamic neoplasm,C0020659,,,MONDO:0006799,hypothalamic neoplasm,
+BMGC_DS01233,BMG_DS001566,267465007;190274003;154660000;237572004;40930008,Hypothyroidism,Hypothyroidism,,,,DOID:1459,hypothyroidism,C0020676,D007037,MTHU002670,MONDO:0005420,hypothyroidism,Hypothyroidism - congenital and acquired (& [cretinism] or [myxedema]) | Cretinism | Hypothyroidism-congen.+ acqui. | Hypothyroidism - congenital and acquired | Hypothyroidism | Myxoedema | Hypothyroidism - congenital and acquired (& [cretinism] or [myxoedema]) | Myxedema | Hypothyroidism - congenital and acquired (& [cretinism] or [myxoedema]) (disorder) | Hypothyroidism | Acquired hypothyroidism | Thyroid deficiency | Hypothyroidism: &/or (acquired) | Myxedema | Myxoedema | Hypothyroidism: &/or (acquired) (disorder) | Cretinism | Hypothyroidism | Hypothyroidism - congenital and acquired | Hypothyroidism-congen.+ acqui. | Hypothyroidism - congenital and acquired (& [cretinism] or [myxedema]) | Hypothyroidism - congenital and acquired (& [cretinism] or [myxoedema]) | Myxedema | Myxoedema | Hypothyroidism - congenital and acquired (& [cretinism] or [myxoedema]) (disorder) | Hypothyroidism | Hypothyroidism (disorder) | Hypothyroidism | Hypothyroid | Hypothyroidism (disorder)
+BMGC_DS01234,BMG_DS001567,53602002,Hypotrichosis,Hypotrichosis,,,,DOID:4535,hypotrichosis,C0020678,D007039,MTHU002744,MONDO:0003037,hypotrichosis,Hypotrichosis | Hypotrichosis (disorder)
+BMGC_DS01235,BMG_DS001569,,Type II Mucolipidosis,Mucolipidoses,,,,,,C0020725,D009081,,,,
+BMGC_DS01236,BMG_DS001570,,Iatrogenic Disease,Iatrogenic Disease,,,,,,C0020732,D007049,,MONDO:0043543,iatrogenic disease,
+BMGC_DS01237,BMG_DS001571,,Ichthyoses,Ichthyosis,,,,DOID:1697,ichthyosis,C0020757,D007057,,MONDO:0019269,ichthyosis,
+BMGC_DS01238,BMG_DS001572,13059002,Congenital ichthyosis,,,,Q80,,,C0020758,,MTHU055329,,,Congenital ichthyosis of skin | Ichthyosis congenita | Congenital ichthyosis | Fish scale disease | Fish skin | Congenital ichthyosis of skin (disorder)
+BMGC_DS01239,BMG_DS001573,,Idiopathic Hypercatabolic Hypoproteinemia,Protein-Losing Enteropathies,,,,,,C0020800,D011504,,,,
+BMGC_DS01240,BMG_DS001574,40527005;190848001,Idiopathic pulmonary hemosiderosis,,,,J84.03,DOID:12118,pulmonary hemosiderosis,C0020807,,178550,MONDO:0008346,pulmonary hemosiderosis,Idiopathic pulmonary hemosiderosis | Brown induration of lung | Pulmonary hemosiderosis | Pulmonary haemosiderosis | Idiopathic pulmonary haemosiderosis | Idiopathic pulmonary hemosiderosis (disorder) | IPH - Idiopathic pulmonary haemosiderosis | IPH - Idiopathic pulmonary hemosiderosis | Idiopathic pulmonary haemosiderosis | Idiopathic pulmonary hemosiderosis | Idiopathic pulmonary haemosiderosis (disorder)
+BMGC_DS01241,BMG_DS001576,,,,,,,DOID:10156,benign ileal neoplasm,C0020876,,,MONDO:0006801,ileal neoplasm,
+BMGC_DS01242,BMG_DS001577,52457000,Ileitis,Ileitis,,,,DOID:0060189,ileitis,C0020877,D007079,MTHU063170,,,Ileitis | Ileitis (disorder)
+BMGC_DS01243,BMG_DS001578,,Immune Complex Diseases,Immune Complex Diseases,,,,DOID:1557,hypersensitivity reaction type III disease,C0020951,D007105,,MONDO:0007004,type III hypersensitivity disease,
+BMGC_DS01244,BMG_DS001579,,,,,,,DOID:0111147,angioimmunoblastic T-cell lymphoma,C0020981,,,MONDO:0004977,angioimmunoblastic T-cell lymphoma,
+BMGC_DS01245,BMG_DS001580,,Immunologic Deficiency Syndromes,Immunologic Deficiency Syndromes,,,,DOID:612,primary immunodeficiency disease,C0021051,D007153,,MONDO:0021094,immunodeficiency disease,
+BMGC_DS01246,BMG_DS001581,,Immune System Diseases,Immune System Diseases,,,,,,C0021053,D007154,,MONDO:0005046,immune system disorder,
+BMGC_DS01247,BMG_DS001582,,,,,,,DOID:2916,hypersensitivity reaction type IV disease,C0021070,,,MONDO:0021334,immunoproliferative disorder,
+BMGC_DS01248,BMG_DS001584,156319000;267836006;48277006,Impetigo,Impetigo,1B72.Z,"Impetigo, unspecified",L01.0;L01,DOID:8504,impetigo,C0021099,D007169,MTHU037496,MONDO:0004592,impetigo,(Impetigo) or (pemphigus neonatorum) | Impetigo | Pemphigus neonatorum | (Impetigo) or (pemphigus neonatorum) (disorder) | Impetigo | Pemphigus neonatorum | (Impetigo) or (pemphigus neonatorum) | (Impetigo) or (pemphigus neonatorum) (disorder) | Impetigo | Impetigo contagiosa | Impetigo (disorder)
+BMGC_DS01249,BMG_DS001586,,,,,,,DOID:10937,impulse control disorder,C0021122,,,MONDO:0001162,impulse control disorder,
+BMGC_DS01250,BMG_DS001587,,Inappropriate ADH Syndrome,Inappropriate ADH Syndrome,,,,DOID:3401,inappropriate ADH syndrome,C0021141,D007177,,MONDO:0006802,inappropriate ADH syndrome,
+BMGC_DS01251,BMG_DS001589,,,,,,,DOID:12305,Bloch-Sulzberger syndrome,C0021171,,308300,MONDO:0010631,incontinentia pigmenti,
+BMGC_DS01252,BMG_DS001590,14386001,Indeterminate leprosy,,1B20.0,Paucibacillary leprosy,A30.0,DOID:11851,indeterminate leprosy,C0021192,,,MONDO:0001391,indeterminate leprosy,Indeterminate leprosy | Group I leprosy | Indeterminate leprosy (disorder) | Type I leprosy
+BMGC_DS01253,BMG_DS001591,,,,,,,DOID:3765,pseudohermaphroditism,C0021193,,,,,
+BMGC_DS01254,BMG_DS001592,,Infant Nutrition Disorders,Infant Nutrition Disorders,,,,,,C0021280,D007228,,,,
+BMGC_DS01255,BMG_DS001593,22925008,Neonatal disorder,,,,,,,C0021290,,,,,Neonatal disease | Neonatal disorder | Neonatal disorder (disorder)
+BMGC_DS01256,BMG_DS001594,,"Infant, Premature, Diseases","Infant, Premature, Diseases",,,,,,C0021295,D007235,,,,
+BMGC_DS01257,BMG_DS001595,266618004,Infection of kidney,,,,,DOID:782,renal infectious disease,C0021313,,,MONDO:0004369,renal infectious disease,Infection of kidney (& [pyelonephritis &/or pyelitis]) | Renal infection | Kidney infection | Infection of kidney | Pyelonephritis/pyelitis | Infection - kidney | Infection of kidney (& [pyelonephritis &/or pyelitis]) (disorder)
+BMGC_DS01258,BMG_DS001597,55184003,Infectious enteritis,,,,,,,C0021342,,MTHU074762,,,Infectious enteritis | Infective enteritis | Infectious enteritis of intestine | Infectious inflammation of intestine (disorder) | Infectious inflammation of intestine
+BMGC_DS01259,BMG_DS001598,,Infectious Mononucleosis,Infectious Mononucleosis,,,,DOID:8568,infectious mononucleosis,C0021345,D007244,,MONDO:0005810,infectious mononucleosis,
+BMGC_DS01260,BMG_DS001599,194198006;86981007;267752002,Infective otitis externa,,,,,DOID:9463,otitis externa,C0021355,,,,,Infective otitis externa | Infective OE | Infective otitis externa (disorder) | Infective otitis externa | Infective otitis externa (disorder) | Infective OE (otitis externa) | Cellulitis - ear | Swimmers ear | Infective otitis externa | (Infective otitis externa (& [cellulitis ear])) or (swimmers ear) | (Infective otitis externa (& [cellulitis ear])) or (swimmers ear) (disorder)
+BMGC_DS01261,BMG_DS001600,,,,,,,DOID:5223,infertility,C0021359,,,MONDO:0005047,infertility disorder,
+BMGC_DS01262,BMG_DS001601,84245004;198011008,Infertility due to extratesticular cause,,,,,DOID:14096,infertility due to extratesticular cause,C0021360,,,MONDO:0001877,infertility due to extratesticular cause,Infertility due to extratesticular cause | Infertility due to extratesticular cause (disorder)
+BMGC_DS01263,BMG_DS001602,,,,,,,,,C0021361,,,MONDO:0021124,female infertility,
+BMGC_DS01264,BMG_DS001603,155924001;2904007,Male infertility,,,,N46,DOID:12336,male infertility,C0021364,,MTHU071905,MONDO:0005372,male infertility,Male infertility | Male infertility (disorder)
+BMGC_DS01265,BMG_DS001604,,Inflammatory Bowel Diseases,Inflammatory Bowel Diseases,,,,DOID:0050589,inflammatory bowel disease,C0021390,D015212,,MONDO:0005265,inflammatory bowel disease,
+BMGC_DS01266,BMG_DS001605,,,,,,,DOID:12105,inflammatory spondylopathy,C0021396,,,,,
+BMGC_DS01267,BMG_DS001606,6142004;155559006,Influenza,"Influenza, Human",,,,DOID:8469,influenza,C0021400,D007251,,MONDO:0005812,influenza,Influenza | Flu | Grippe | Influenza (disorder) | Influenza | Influenza (disorder)
+BMGC_DS01268,BMG_DS001608,,,,,,,DOID:4706,infratentorial cancer,C0021432,,,MONDO:0037736,infratentorial neoplasm,
+BMGC_DS01269,BMG_DS001609,,Disorders of Environmental Origin,Disorders of Environmental Origin,,,,,,C0021508,D007280,,,,
+BMGC_DS01270,BMG_DS001611,,Sleep Initiation and Maintenance Disorders,Sleep Initiation and Maintenance Disorders,,,,,,C0021603,D007319,,MONDO:0024376,"sleep disorder, initiating and maintaining sleep",
+BMGC_DS01271,BMG_DS001613,,,,,,,DOID:3892,insulinoma,C0021670,,,MONDO:0024677,pancreatic insulinoma,
+BMGC_DS01272,BMG_DS001614,,Intermittent Claudication,Intermittent Claudication,,,,DOID:3669,intermittent claudication,C0021775,D007383,,MONDO:0005295,intermittent vascular claudication,
+BMGC_DS01273,BMG_DS001615,,,,,,,DOID:12401,intermittent explosive disorder,C0021776,,,MONDO:0001521,intermittent explosive disorder,
+BMGC_DS01274,BMG_DS001617,,Intervertebral Disk Displacement,Intervertebral Disc Displacement,,,,,,C0021818,D007405,,,,
+BMGC_DS01275,BMG_DS001619,,Intestinal Atresia,Intestinal Atresia,,,,DOID:10486,intestinal atresia,C0021828,D007409,,MONDO:0001045,intestinal atresia,
+BMGC_DS01276,BMG_DS001620,,,,,,,DOID:9868,intestinal disaccharidase deficiency,C0021830,,,,,
+BMGC_DS01277,BMG_DS001621,,Intestinal Diseases,Intestinal Diseases,,,,DOID:5295,intestinal disease,C0021831,D007410,,MONDO:0005020,intestinal disorder,
+BMGC_DS01278,BMG_DS001622,,"Intestinal Diseases, Parasitic","Intestinal Diseases, Parasitic",,,,,,C0021832,D007411,,MONDO:0024270,parasitic intestinal disorder,
+BMGC_DS01279,BMG_DS001624,,,,,,,DOID:4610,intestinal benign neoplasm,C0021841,,,MONDO:0021118,intestinal neoplasm,
+BMGC_DS01280,BMG_DS001625,,Intestinal Obstruction,Intestinal Obstruction,,,,DOID:8437,intestinal obstruction,C0021843,D007415,,MONDO:0004565,intestinal obstruction,
+BMGC_DS01281,BMG_DS001626,,Intestinal Perforation,Intestinal Perforation,,,,DOID:2074,intestinal perforation,C0021845,D007416,,MONDO:0006807,intestinal perforation,
+BMGC_DS01282,BMG_DS001627,,,,,,,,,C0021846,,,MONDO:0005288,intestinal polyp,
+BMGC_DS01283,BMG_DS001628,,Intestinal Pseudo-Obstruction,Intestinal Pseudo-Obstruction,,,,DOID:0080072,intestinal pseudo-obstruction,C0021847,D007418,,MONDO:0002803,intestinal pseudo-obstruction,
+BMGC_DS01284,BMG_DS001630,27614006;192738001,Intracranial abscess,,,,,DOID:10095,intracranial abscess,C0021874,,,MONDO:0000939,intracranial abscess,Intracranial abscess | Intracranial abscess (disorder) | Brain abscess | Intracranial abscess | Intracranial abscess(& [brain]) | Intracranial abscess(& [brain]) (disorder)
+BMGC_DS01285,BMG_DS001632,155772009;35327006,Intussusception,Intussusception,DE2Z,"Diseases of the digestive system, unspecified",K56.1,DOID:8446,intussusception,C0021933,D007443,MTHU016100;147710,MONDO:0007835,intussusception,Intussusception | Intussusception (disorder) | Intussusception | Introsusception | Intussusception (morphologic abnormality)
+BMGC_DS01286,BMG_DS001637,77971008;193481009,Iridocyclitis,Iridocyclitis,,,H20,,,C0022073,D015863,MTHU037137,MONDO:0004773,iridocyclitis,Iridocyclitis | Iridocyclitis (disorder) | Disorders of iris &/or ciliary body (& [iridocyclitis]) | Ciliary body disorders | Iridocyclitis | Disorders of iris and ciliary body | Disorders of iris &/or ciliary body (& [iridocyclitis]) (disorder)
+BMGC_DS01287,BMG_DS001638,,Iris Diseases,Iris Diseases,,,,DOID:240,iris disease,C0022078,D007499,,MONDO:0002289,iris disorder,
+BMGC_DS01288,BMG_DS001639,,,,,,,DOID:3478,iris cancer,C0022079,,,MONDO:0021224,iris neoplasm,
+BMGC_DS01289,BMG_DS001640,65074000,Iritis,Iritis,,,,DOID:1406,iritis,C0022081,D007500,MTHU026370,MONDO:0006814,iritis,Iritis | Iritis (disorder)
+BMGC_DS01290,BMG_DS001641,,Irritable Bowel Syndrome,Irritable Bowel Syndrome,,,,DOID:9778,irritable bowel syndrome,C0022104,D043183,,MONDO:0005052,irritable bowel syndrome,
+BMGC_DS01291,BMG_DS001642,,,,,,,DOID:326,ischemia,C0022116,,,MONDO:0005053,ischemic disease,
+BMGC_DS01292,BMG_DS001644,,,,,,,DOID:3892,insulinoma,C0022134,,,,,
+BMGC_DS01293,BMG_DS001645,,,,,,,DOID:3156,hypomelanosis of Ito,C0022283,,300337,MONDO:0010302,Ito hypomelanosis,
+BMGC_DS01294,BMG_DS001646,,Jacksonian Seizure,Seizures,,,,,,C0022333,D012640,,,,
+BMGC_DS01295,BMG_DS001647,155061007;792004,Creutzfeldt-Jakob disease,,8E02.0,Genetic CreutzfeldtJakob disease,A81.0,DOID:11949,Creutzfeldt-Jakob disease,C0022336,,,MONDO:0005357,Creutzfeldt Jacob disease,Creutzfeldt-Jakob disease | Creutzfeldt-Jakob disease (disorder) | Jakob-Creutzfeldt disease | Creutzfeldt-Jakob disease | Subacute spongiform encephalopathy | Jakob-Creutzfeldt disease (disorder) | CJD - Creutzfeldt-Jakob disease | JCD - Jakob-Creutzfeldt disease | Transmissible virus dementia
+BMGC_DS01296,BMG_DS001648,,Late-Infantile Neuronal Ceroid Lipofuscinosis,Neuronal Ceroid-Lipofuscinoses,,,,,,C0022340,D009472,,MONDO:0015674,late infantile neuronal ceroid lipofuscinosis,
+BMGC_DS01297,BMG_DS001649,,"Jaundice, Chronic Idiopathic","Jaundice, Chronic Idiopathic",,,,DOID:12308,Dubin-Johnson syndrome,C0022350,D007566,237500,MONDO:0009380,Dubin-Johnson syndrome,
+BMGC_DS01298,BMG_DS001650,,,,,,,DOID:2383,neonatal jaundice,C0022353,,,,,
+BMGC_DS01299,BMG_DS001651,,"Jaundice, Obstructive","Jaundice, Obstructive",,,,DOID:13603,obstructive jaundice,C0022354,D041781,,MONDO:0006874,obstructive jaundice,
+BMGC_DS01300,BMG_DS001652,,Jaw Diseases,Jaw Diseases,,,,,,C0022362,D007571,,,,
+BMGC_DS01301,BMG_DS001653,,,,,,,DOID:1862,jaw cancer,C0022364,,,MONDO:0021580,neoplasm of jaw,
+BMGC_DS01302,BMG_DS001656,,Jejunal Diseases,Jejunal Diseases,,,,,,C0022373,D007579,,,,
+BMGC_DS01303,BMG_DS001657,,,,,,,DOID:3218,jejunal neoplasm,C0022374,,,MONDO:0002564,jejunal neoplasm,
+BMGC_DS01304,BMG_DS001658,,Jervell-Lange Nielsen Syndrome,Jervell-Lange Nielsen Syndrome,,,,DOID:2842,Jervell-Lange Nielsen syndrome,C0022387,D029593,,MONDO:0002441,Jervell and Lange-Nielsen syndrome,
+BMGC_DS01305,BMG_DS001659,399269003;268051001;8316001,Arthropathy,Joint Diseases,,,,DOID:381,arthropathy,C0022408,D007592,MTHU012515,MONDO:0006816,arthropathy,Arthropathy (disorder) | Arthropathy | Arthrosis | Joint disorder | Joint disease | Disorder of joint | (Arthritis/arthrosis) or (arthropathy) or (joint disorders) | Arthritis/arthrosis | Joint disorders | Arthropathy | (Arthritis/arthrosis) or (arthropathy) or (joint disorders) (disorder) | Arthropathy | Disorder of joint | Joint disease | Arthrosis | Joint derangement | Joint disorder | Arthropathy (disorder)
+BMGC_DS01306,BMG_DS001661,15739006,Juvenile osteochondrosis of hip AND/OR pelvis,,,,,DOID:14415,Legg-Calve-Perthes disease,C0022441,,,,,Juvenile osteochondrosis of hip AND/OR pelvis (disorder) | Juvenile osteochondritis of hip AND/OR pelvis
+BMGC_DS01307,BMG_DS001663,,Kartagener Syndrome,Kartagener Syndrome,,,,DOID:0050144,Kartagener syndrome,C0022521,D007619,,,,
+BMGC_DS01308,BMG_DS001664,25792000,Kearns-Sayre syndrome,,,,H49.81,DOID:12934,Kearns-Sayre syndrome,C0022541,,530000,MONDO:0010787,Kearns-Sayre syndrome,Kearns-Sayre syndrome | Kearns-Sayre syndrome (disorder) | Kearns-Sayre mitochondrial cytopathy | Mitochondrial ocular myopathy | KSS - Kearns-Sayre syndrome | Oculocraniosomatic syndrome
+BMGC_DS01309,BMG_DS001665,,,,,,,,,C0022548,,,MONDO:0005348,keloid,
+BMGC_DS01310,BMG_DS001666,5888003;193757003;155151002,Keratitis,Keratitis,,,H16,DOID:4677,keratitis,C0022568,D007634,MTHU036935,MONDO:0003085,keratitis,Keratitis | Keratitis (disorder) | Keratitis &/or keratoconjunctivitis | Keratitis | Keratoconjunctivitis | Keratitis &/or keratoconjunctivitis (disorder)
+BMGC_DS01311,BMG_DS001667,,"Keratitis, Dendritic","Keratitis, Dendritic",,,,,,C0022570,D007635,,,,
+BMGC_DS01312,BMG_DS001668,,,,,,,DOID:3149,keratoacanthoma,C0022572,,,MONDO:0002527,keratoacanthoma,
+BMGC_DS01313,BMG_DS001669,88151007;193757003;155154005,Keratoconjunctivitis,Keratoconjunctivitis,9A7Y,Other specified disorders of the cornea,H16.2,DOID:9368,keratoconjunctivitis,C0022573,D007637,MTHU036934,MONDO:0004768,keratoconjunctivitis,Keratoconjunctivitis | Superficial keratitis with conjunctivitis | Keratoconjunctivitis (disorder) | Keratitis &/or keratoconjunctivitis | Keratitis | Keratoconjunctivitis | Keratitis &/or keratoconjunctivitis (disorder) | Keratoconjunctivitis | Keratoconjunctivitis (disorder)
+BMGC_DS01314,BMG_DS001670,,Keratoconjunctivitis Sicca,Keratoconjunctivitis Sicca,,,,DOID:12895,keratoconjunctivitis sicca,C0022575,D007638,,MONDO:0000948,xerophthalmia,
+BMGC_DS01315,BMG_DS001672,,"Keratoconjunctivitis, Vernal","Conjunctivitis, Allergic",,,,,,C0022577,D003233,,MONDO:0019085,vernal keratoconjunctivitis,
+BMGC_DS01316,BMG_DS001673,65636009;155160005;267733008,Keratoconus,Keratoconus,9A78.50,Keratoconus,H18.6,DOID:10126,keratoconus,C0022578,D007640,MTHU036426,MONDO:0015486,keratoconus,Keratoconus | Keratoconus (disorder) | Cornea conical | (Keratoconus) or (corneal disorders NOS) | Corneal disorders NOS | Keratoconus | Corneal disorder NOS | (Keratoconus) or (corneal disorders NOS) (disorder) | Corneal disorder NOS | Keratoconus | Corneal disorders NOS | (Keratoconus) or (corneal disorders NOS) | (Keratoconus) or (corneal disorders NOS) (disorder)
+BMGC_DS01317,BMG_DS001675,,,,,,,DOID:13072,acquired hyperkeratosis,C0022581,,,MONDO:0006522,acquired keratosis,
+BMGC_DS01318,BMG_DS001676,,"Keratoderma, Palmoplantar, Diffuse","Keratoderma, Palmoplantar, Diffuse",,,,,,C0022584,D015776,,MONDO:0017666,diffuse palmoplantar keratoderma,
+BMGC_DS01319,BMG_DS001677,254666005,Keratosis,Keratosis,,,,DOID:161,keratosis,C0022593,D007642,,MONDO:0006566,keratosis,Keratosis | Keratosis (disorder) | Hyperkeratosis
+BMGC_DS01320,BMG_DS001678,,Keratosis Blennorrhagica,Keratosis,,,,,,C0022594,D007642,,,,
+BMGC_DS01321,BMG_DS001679,,Keratosis Follicularis,Darier Disease,,,,DOID:2734,keratosis follicularis,C0022595,D007644,124200,MONDO:0007417,Darier disease,
+BMGC_DS01322,BMG_DS001680,,,,,,,DOID:3390,palmoplantar keratosis,C0022596,,,MONDO:0006590,palmoplantar keratosis,
+BMGC_DS01323,BMG_DS001681,,,,,,,DOID:8866,actinic keratosis,C0022602,,,MONDO:0005173,actinic keratosis,
+BMGC_DS01324,BMG_DS001682,,,,,,,DOID:6498,seborrheic keratosis,C0022603,,182000,MONDO:0008420,seborrheic keratosis,
+BMGC_DS01325,BMG_DS001683,268880009;74925009;157135006;230770008,Kernicterus,Kernicterus,,,P57,DOID:2382,kernicterus,C0022610,D007647,MTHU037351,MONDO:0018477,bilirubin encephalopathy,Kernicterus (& [due to isoimmunization]) | Kernicterus (& [due to isoimmunisation]) | Kernicterus due to isoimmunization | Kernicterus due to isoimmunisation | Kernicterus | Kernicterus - due to isoimm. | Kernicterus (& [due to isoimmunisation]) (disorder) | Kernicterus | Nuclear jaundice | Kernicterus (morphologic abnormality) | Kernicterus - due to isoimm. | Kernicterus | Kernicterus (& [due to isoimmunization]) | Kernicterus (& [due to isoimmunisation]) | Kernicterus due to isoimmunisation | Kernicterus due to isoimmunization | Kernicterus (& [due to isoimmunisation]) (disorder) | Kernicterus | Kernicterus (disorder)
+BMGC_DS01326,BMG_DS001685,,Kidney Cortex Necrosis,Kidney Cortex Necrosis,,,,DOID:2973,kidney cortex necrosis,C0022656,D007673,,MONDO:0006820,kidney cortex necrosis,
+BMGC_DS01327,BMG_DS001686,,Kidney Diseases,Kidney Diseases,,,,DOID:557,kidney disease,C0022658,D007674,,MONDO:0005240,kidney disorder,
+BMGC_DS01328,BMG_DS001687,,"Kidney Failure, Acute",Acute Kidney Injury,,,,DOID:3021,acute kidney failure,C0022660,D058186,,,,
+BMGC_DS01329,BMG_DS001688,,"Kidney Failure, Chronic","Kidney Failure, Chronic",,,,DOID:784,chronic kidney disease,C0022661,D007676,,MONDO:0024327,chronic renal failure syndrome,
+BMGC_DS01330,BMG_DS001689,,,,,,,DOID:263,kidney cancer,C0022665,,,MONDO:0021163,kidney neoplasm,
+BMGC_DS01331,BMG_DS001690,,Kidney Papillary Necrosis,Kidney Papillary Necrosis,,,,DOID:2981,kidney papillary necrosis,C0022667,D007681,,MONDO:0006821,kidney papillary necrosis,
+BMGC_DS01332,BMG_DS001691,,Acute Kidney Tubular Necrosis,"Kidney Tubular Necrosis, Acute",,,,DOID:12556,acute kidney tubular necrosis,C0022672,D007683,,MONDO:0006637,acute kidney tubular necrosis,
+BMGC_DS01333,BMG_DS001692,,Cystic kidney,,,,,DOID:2975,cystic kidney disease,C0022679,,MTHU011852,,,
+BMGC_DS01334,BMG_DS001693,,Polycystic Kidney Diseases,Polycystic Kidney Diseases,,,,DOID:898,autosomal dominant polycystic kidney disease,C0022680,D007690,,MONDO:0020642,polycystic kidney disease,
+BMGC_DS01335,BMG_DS001694,204959000;236443009;29780007,Medullary sponge kidney,,,,,,,C0022681,,MTHU067062,MONDO:0015268,medullary sponge kidney,"Medullary cystic disease, adult type | Medullary sponge kidney | Medullary: [cystic disease, adult type] or [sponge kidney] | Medullary: [cystic disease, adult type] or [sponge kidney] (disorder) | Medullary sponge kidney | Medullary sponge kidney (disorder) | Medullary cystic disease of the kidney | Medullary cystic disease of the kidney (disorder)"
+BMGC_DS01336,BMG_DS001695,,Kienbock Disease,Osteonecrosis,,,,,,C0022682,D010020,,MONDO:0019967,Kienbock disease,
+BMGC_DS01337,BMG_DS001696,,Menkes Kinky Hair Syndrome,Menkes Kinky Hair Syndrome,,,,DOID:1838,Menkes disease,C0022716,D007706,309400,MONDO:0010651,Menkes disease,
+BMGC_DS01338,BMG_DS001697,,Klebsiella Infections,Klebsiella Infections,,,,DOID:13272,Klebsiella pneumonia,C0022729,D007710,,MONDO:0030603,Klebsiella infectious disease,
+BMGC_DS01339,BMG_DS001698,,,,,,,DOID:12400,kleptomania,C0022734,,,MONDO:0001520,kleptomania,
+BMGC_DS01340,BMG_DS001699,,Klinefelter Syndrome,Klinefelter Syndrome,,,,DOID:1921,Klinefelter syndrome,C0022735,D007713,,MONDO:0006823,Klinefelter syndrome,
+BMGC_DS01341,BMG_DS001700,,Klippel-Feil Syndrome,Klippel-Feil Syndrome,,,,DOID:10426,Klippel-Feil syndrome,C0022738,D007714,,MONDO:0001029,Klippel-Feil syndrome,
+BMGC_DS01342,BMG_DS001701,,Klippel-Trenaunay-Weber Syndrome,Klippel-Trenaunay-Weber Syndrome,,,,DOID:2926,Klippel-Trenaunay syndrome,C0022739,D007715,149000,MONDO:0007864,angioosteohypertrophic syndrome,
+BMGC_DS01343,BMG_DS001702,,,,,,,DOID:8738,leukoplakia of penis,C0022782,,,MONDO:0006830,leukoplakia of penis,
+BMGC_DS01344,BMG_DS001703,,Vulvar Lichen Sclerosus,Vulvar Lichen Sclerosus,,,,,,C0022783,D007724,,MONDO:0006491,vulvar lichen sclerosus,
+BMGC_DS01345,BMG_DS001704,,,,,,,DOID:9597,Krukenberg carcinoma,C0022790,,,MONDO:0004829,Krukenberg carcinoma,
+BMGC_DS01346,BMG_DS001705,,Adult Neuronal Ceroid Lipofuscinosis,Neuronal Ceroid-Lipofuscinoses,,,,,,C0022797,D009472,,MONDO:0019260,adult neuronal ceroid lipofuscinosis,
+BMGC_DS01347,BMG_DS001706,86188000;192684001,Kuru,Kuru,,,A81.81,DOID:648,kuru,C0022802,D007729,,MONDO:0006825,kuru,Kuru | Kuru (disorder) | Kuru encephalitis | Kuru | Kuru (disorder)
+BMGC_DS01348,BMG_DS001707,267495004;58262005;154730001,Kwashiorkor,Kwashiorkor,,,E40,DOID:13579,kwashiorkor,C0022806,D007732,,MONDO:0006826,kwashiorkor,Nutritional deficiencies: (& [dietary] or [kwashiokor] or [marasmus]) | Dietary deficiency | Marasmus | Insufficiency - dietary | Nutritional deficiencies | Deficiency -nutritional | Kwashiorkor | Kwashiokor | Nutritional deficiencies: (& [dietary] or [kwashiokor] or [marasmus]) (disorder) | Kwashiorkor | Malignant malnutrition | Deposed child syndrome | Fatty liver of Brahmin children | Protein malnutrition | Nutritional edema with dyspigmentation of skin AND/OR hair | Nutritional oedema with dyspigmentation of skin AND/OR hair | Kwashiorkor (disorder) | Kwashiokor | Deficiency -nutritional | Marasmus | Kwashiorkor | Nutritional deficiencies | Insufficiency - dietary | Dietary deficiency | Nutritional deficiencies: (& [dietary] or [kwashiokor] or [marasmus]) | Nutritional deficiencies: (& [dietary] or [kwashiokor] or [marasmus]) (disorder)
+BMGC_DS01349,BMG_DS001708,,Kyasanur Forest Disease,Kyasanur Forest Disease,,,,DOID:11320,Kyasanur forest disease,C0022810,D007733,,MONDO:0017881,Kyasanur forest disease,
+BMGC_DS01350,BMG_DS001710,20425006,Labyrinthine disorder,,,,,DOID:2952,inner ear disease,C0022890,,,,,Labyrinthine disorder | Labyrinthine vertigo | Vestibular disorder | Central vestibular vertigo | Labyrinthine disorder (disorder)
+BMGC_DS01351,BMG_DS001711,155239008;23919004,Labyrinthitis,Labyrinthitis,AB30.1,Labyrinthitis,H83.0,DOID:1468,labyrinthitis,C0022893,D007762,,MONDO:0002008,labyrinthitis,Labyrinthitis | Labyrinthitis (disorder)
+BMGC_DS01352,BMG_DS001712,,Lacrimal Apparatus Diseases,Lacrimal Apparatus Diseases,,,,DOID:1400,lacrimal apparatus disease,C0022904,D007766,,MONDO:0001854,lacrimal apparatus disorder,
+BMGC_DS01353,BMG_DS001713,,,,,,,DOID:13929,lacrimal duct obstruction,C0022906,,,,,
+BMGC_DS01354,BMG_DS001714,,Lactation Disorder,Lactation Disorders,,,,,,C0022927,D007775,,MONDO:0045019,lactation disease,
+BMGC_DS01355,BMG_DS001715,,Lactose Intolerance,Lactose Intolerance,,,,DOID:10604,lactose intolerance,C0022951,D007787,,MONDO:0100345,lactose intolerance,
+BMGC_DS01356,BMG_DS001717,,Lambert-Eaton Myasthenic Syndrome,Lambert-Eaton Myasthenic Syndrome,,,,DOID:0050214,Lambert-Eaton myasthenic syndrome,C0022972,D015624,,MONDO:0018556,Lambert-Eaton myasthenic syndrome,
+BMGC_DS01357,BMG_DS001719,,Langer-Giedion Syndrome,Langer-Giedion Syndrome,,,,DOID:4998,trichorhinophalangeal syndrome type II,C0023003,D015826,150230,MONDO:0007874,trichorhinophalangeal syndrome type II,
+BMGC_DS01358,BMG_DS001721,,,,,,,DOID:93,language disorder,C0023015,,,MONDO:0004750,language disorder,
+BMGC_DS01359,BMG_DS001723,,"Larva Migrans, Visceral","Larva Migrans, Visceral",,,,DOID:9790,toxocariasis,C0023049,D007816,,MONDO:0024954,"larva migrans, visceral",
+BMGC_DS01360,BMG_DS001724,,Laryngeal Diseases,Laryngeal Diseases,,,,DOID:786,laryngeal disease,C0023051,D007818,,MONDO:0004382,laryngeal disorder,
+BMGC_DS01361,BMG_DS001725,,,,,,,DOID:2598,laryngeal benign neoplasm,C0023055,,,MONDO:0021071,laryngeal neoplasm,
+BMGC_DS01362,BMG_DS001726,,Laryngeal Perichondritis,Laryngeal Diseases,,,,,,C0023059,D007818,,,,
+BMGC_DS01363,BMG_DS001727,406444002;42006002;29331000;195868005,Laryngospasm,Laryngismus,,,,,,C0023066,D007826,MTHU001729,,,Laryngeal spasm (disorder) | Laryngeal spasm | Laryngospasm | Laryngeal spasm | Laryngospasm | Laryngismus stridulus | Laryngeal spasm (disorder) | Laryngospasm | Laryngospasm (finding) | Laryngospasm | Laryngospasm (disorder)
+BMGC_DS01364,BMG_DS001728,45913009,Laryngitis,Laryngitis,,,,DOID:3437,laryngitis,C0023067,D007827,,MONDO:0002647,laryngitis,Laryngitis | Laryngitis (disorder)
+BMGC_DS01365,BMG_DS001730,,,,,,,DOID:11527,laryngostenosis,C0023075,,,MONDO:0001305,laryngostenosis,
+BMGC_DS01366,BMG_DS001733,,Lassa Fever,Lassa Fever,,,,DOID:9537,Lassa fever,C0023092,D007835,,MONDO:0005820,Lassa fever,
+BMGC_DS01367,BMG_DS001734,,Laurence-Moon Syndrome,Laurence-Moon Syndrome,,,,DOID:1930,Laurence-Moon syndrome,C0023138,D007849,245800,MONDO:0009514,Laurence-Moon syndrome,
+BMGC_DS01368,BMG_DS001736,,,,,,,DOID:8927,learning disability,C0023186,,,,,
+BMGC_DS01369,BMG_DS001737,1264565005,Familial lecithin cholesterol acyltransferase deficiency,,,,,DOID:1391,Norum disease,C0023195,,245900,MONDO:0009515,Norum disease,Familial lecithin cholesterol acyltransferase deficiency (disorder) | Familial lecithin cholesterol acyltransferase deficiency | Complete LCAT deficiency | Norum disease | Complete LCAT (lecithin-cholesterol acyltransferase) deficiency
+BMGC_DS01370,BMG_DS001738,,Left Bundle-Branch Block,Bundle-Branch Block,,,,,,C0023211,D002037,,,,
+BMGC_DS01371,BMG_DS001739,,Left-Sided Heart Failure,Heart Failure,,,,,,C0023212,D006333,,,,
+BMGC_DS01372,BMG_DS001741,,Leg Dermatoses,Leg Dermatoses,,,,DOID:3142,leg dermatosis,C0023219,D007868,,MONDO:0006569,leg dermatosis,
+BMGC_DS01373,BMG_DS001742,,Leg Ulcer,Leg Ulcer,,,,,,C0023223,D007871,,MONDO:0004601,ulcer of lower limbs,
+BMGC_DS01374,BMG_DS001743,240241003,Coxa plana (disorder),,,,,DOID:14415,Legg-Calve-Perthes disease,C0023234,,,,,Coxa plana | Coxa plana (disorder)
+BMGC_DS01375,BMG_DS001744,26726000,Legionellosis,Legionellosis,,,,DOID:10458,legionellosis,C0023240,D007876,,MONDO:0005823,legionellosis,Legionella infection | Legionellosis | Legionella infection (disorder)
+BMGC_DS01376,BMG_DS001745,,Legionnaires' Disease,Legionnaires' Disease,,,,DOID:10457,Legionnaires' disease,C0023241,D007877,,MONDO:0005824,Legionnaires' disease,
+BMGC_DS01377,BMG_DS001746,,Leigh Disease,Leigh Disease,,,,DOID:3652,Leigh disease,C0023264,D007888,,,,
+BMGC_DS01378,BMG_DS001747,,,,,,,DOID:127,leiomyoma,C0023267,,,MONDO:0001572,leiomyoma,
+BMGC_DS01379,BMG_DS001748,,,,,,,DOID:1967,leiomyosarcoma,C0023269,,,MONDO:0005058,leiomyosarcoma,
+BMGC_DS01380,BMG_DS001749,266206004;154377009;80612004,Leishmaniasis,Leishmaniasis,,,B55,DOID:9065,leishmaniasis,C0023281,D007896,,MONDO:0011989,leishmaniasis,(Rickettsioses/arthropod NOS) or (leishmaniasis) | Leishmaniasis | Rickettsioses/arthropod NOS | (Rickettsioses/arthropod NOS) or (leishmaniasis) (disorder) | Leishmaniasis | Leishmaniosis | Leishmaniasis (disorder)
+BMGC_DS01381,BMG_DS001750,,"Leishmaniasis, Cutaneous","Leishmaniasis, Cutaneous",,,,DOID:9111,cutaneous leishmaniasis,C0023283,D016773,,MONDO:0005446,cutaneous leishmaniasis,
+BMGC_DS01382,BMG_DS001755,,"Leishmaniasis, Visceral","Leishmaniasis, Visceral",,,,DOID:9146,visceral leishmaniasis,C0023290,D007898,,MONDO:0005445,visceral leishmaniasis,
+BMGC_DS01383,BMG_DS001756,,Lens Diseases,Lens Diseases,,,,DOID:110,lens disease,C0023308,D007905,,,,
+BMGC_DS01384,BMG_DS001757,,Lens Dislocation and Subluxation,Lens Subluxation,,,,,,C0023310,D007906,,,,
+BMGC_DS01385,BMG_DS001758,,Lens Subluxation,Lens Subluxation,,,,DOID:11364,lens subluxation,C0023316,D007906,,MONDO:0001271,lens subluxation,
+BMGC_DS01386,BMG_DS001759,156438005;767376003;398744007;75534002;267870007;201286007,Lentigo,Lentigo,ED60.Z,Hypermelanosis of unspecified aetiology,L81.4,,,C0023321,D007911,150900,MONDO:0021582,lentigo,Dyschromia NOS | Freckles | Melanosis | Lentigo | (Dyschromia NOS) or (freckles) or (lentigo) or (melanosis) | (Dyschromia NOS) or (freckles) or (lentigo) or (melanosis) (disorder) | Lentigo (morphologic abnormality) | Lentigo | Lentigo (disorder) | Lentigo | Lentigo | Lentigo simplex | Nevus spilus | Naevus spilus | Speckled lentiginous naevus | Speckled lentiginous nevus | Lentigo (disorder) | Lentigo | Freckles | Dyschromia NOS | Melanosis | (Dyschromia NOS) or (freckles) or (lentigo) or (melanosis) | (Dyschromia NOS) or (freckles) or (lentigo) or (melanosis) (disorder) | Lentigo | Lentigo (disorder)
+BMGC_DS01387,BMG_DS001760,154298007;266184007;81004002,Leprosy,Leprosy,,,,DOID:1024,leprosy,C0023343,D007918,,MONDO:0005124,leprosy,Leprosy and other mycobacterial disorders | Leprosy | Leprosy + other mycobact. dis. | Mycobacterial disease | (Leprosy + other mycobact dis) or (mycobacterial disease) | (Leprosy + other mycobact dis) or (mycobacterial disease) (disorder) | Leprosy | Leprosy and other mycobacterial disorders | Leprosy + other mycobact. dis. | Mycobacterial disease | (Leprosy + other mycobact dis) or (mycobacterial disease) | (Leprosy + other mycobact dis) or (mycobacterial disease) (disorder) | Leprosy | Hansen's disease | Infection due to Mycobacterium leprae | Mycobacterium leprae infection | Leprosy (disorder)
+BMGC_DS01388,BMG_DS001761,50521002;400008009,Borderline leprosy,,1B20.1,Multibacillary leprosy,A30.3,DOID:1023,borderline leprosy,C0023346,,,MONDO:0005125,borderline leprosy,Borderline leprosy | Dimorphic leprosy | Group B leprosy | Type BB leprosy | Midborderline leprosy | BB - Borderline leprosy | Borderline leprosy (disorder) | Borderline leprosy (disorder) | Borderline leprosy | Group B leprosy
+BMGC_DS01389,BMG_DS001762,,"Leprosy, Lepromatous","Leprosy, Lepromatous",,,,DOID:10887,lepromatous leprosy,C0023348,D015440,,MONDO:0005127,lepromatous leprosy,
+BMGC_DS01390,BMG_DS001763,70143003,Tuberculoid leprosy,,1B20.0,Paucibacillary leprosy,A30.1,DOID:1025,tuberculoid leprosy,C0023351,,,MONDO:0005126,tuberculoid leprosy,Tuberculoid leprosy | Type T leprosy | Smooth leprosy | Nodular leprosy | Tuberculoid leprosy (disorder) | Full tuberculoid leprosy | Type TT leprosy | TT - Full tuberculoid leprosy | Tuberculoid Hansen's disease (leprosy)
+BMGC_DS01391,BMG_DS001765,154391003;266213004;77377001;186953000,Leptospirosis,Leptospirosis,,,A27,DOID:2297,leptospirosis,C0023364,D007922,,MONDO:0005825,leptospirosis,Angina - Vincents | Leptospirosis | Chancroid | Weil's disease | Yaws | Vincent's angina | Trench mouth | Lymphogranuloma venereum | Spirochaete disease: [other venereal] or [Vincent's angina] or [chancroid] or [leptospirosis] or [lymphogranuloma venereum] or [trench mouth] or [Weil's disease] or [Yaws] | Other venereal/spirochaete dis | Other venereal/spirochaete disease | Spirochaete disease: [other venereal] or [Vincent's angina] or [chancroid] or [leptospirosis] or [lymphogranuloma venereum] or [trench mouth] or [Weil's disease] or [Yaws] (disorder) | Other venereal/spirochaete disease | Lymphogranuloma venereum | Leptospirosis | Chancroid | Yaws | Vincent's angina | Trench mouth | Angina - Vincents | Weil's disease | Spirochaete disease: [other venereal] or [Vincent's angina] or [chancroid] or [leptospirosis] or [lymphogranuloma venereum] or [trench mouth] or [Weil's disease] or [Yaws] | Spirochaete disease: [other venereal] or [Vincent's angina] or [chancroid] or [leptospirosis] or [lymphogranuloma venereum] or [trench mouth] or [Weil's disease] or [Yaws] (disorder) | Leptospirosis | Infection due to Leptospira | Spirochaetal jaundice | Spirochetal jaundice | Seven day fever | Cane cutter's fever | Harvest fever | Japanese autumnal fever | Queensland fever | Rice-field worker's disease | Leptospirosis (disorder) | Spirochetal jaundice | Leptospirosis | Mud fever | Swamp fever | Cane cutter's fever | Harvest fever | Pretibial fever | Red water fever | Seven day fever | Japanese autumnal fever | Fort Bragg fever | Queensland fever | Rice-field worker's disease | Spirochaetal jaundice | Leptospirosis (disorder)
+BMGC_DS01392,BMG_DS001768,,Lesch-Nyhan Syndrome,Lesch-Nyhan Syndrome,,,,DOID:1919,Lesch-Nyhan syndrome,C0023374,D007926,300322,MONDO:0010298,Lesch-Nyhan syndrome,
+BMGC_DS01393,BMG_DS001769,,Letterer-Siwe Disease,"Histiocytosis, Langerhans-Cell",,,,DOID:2571,Langerhans-cell histiocytosis,C0023381,D006646,246400,MONDO:0009519,letterer-Siwe disease,
+BMGC_DS01394,BMG_DS001770,,,,,,,DOID:1240,leukemia,C0023418,,,MONDO:0005059,leukemia,
+BMGC_DS01395,BMG_DS001771,,,,,,,DOID:1040,chronic lymphocytic leukemia,C0023434,,151400,MONDO:0004948,B-cell chronic lymphocytic leukemia,
+BMGC_DS01396,BMG_DS001772,,,,,,,,,C0023437,,,MONDO:0019458,acute basophilic leukemia,
+BMGC_DS01397,BMG_DS001773,,,,,,,,,C0023440,,,MONDO:0017858,acute erythroid leukemia,
+BMGC_DS01398,BMG_DS001774,,,,,,,DOID:285,hairy cell leukemia,C0023443,,,MONDO:0018935,hairy cell leukemia,
+BMGC_DS01399,BMG_DS001775,,,,,,,DOID:1037,lymphoid leukemia,C0023448,,,MONDO:0005402,lymphoid leukemia,
+BMGC_DS01400,BMG_DS001776,,,,,,,DOID:9952,acute lymphoblastic leukemia,C0023449,,,MONDO:0004967,acute lymphoblastic leukemia,
+BMGC_DS01401,BMG_DS001777,,,,,,,,,C0023452,,,MONDO:0000870,childhood acute lymphoblastic leukemia,
+BMGC_DS01402,BMG_DS001778,,,,,,,DOID:9254,mast-cell leukemia,C0023461,,,MONDO:0020334,mast cell leukemia,
+BMGC_DS01403,BMG_DS001779,,,,,,,DOID:8761,acute megakaryocytic leukemia,C0023462,,,MONDO:0018872,acute megakaryoblastic leukemia,
+BMGC_DS01404,BMG_DS001780,,,,,,,DOID:9953,acute biphenotypic leukemia,C0023464,,,MONDO:0020322,acute biphenotypic leukemia,
+BMGC_DS01405,BMG_DS001781,,,,,,,DOID:8864,acute monocytic leukemia,C0023465,,151380,MONDO:0007896,acute monocytic leukemia,
+BMGC_DS01406,BMG_DS001782,,,,,,,DOID:8593,chronic monocytic leukemia,C0023466,,,MONDO:0004614,chronic monocytic leukemia,
+BMGC_DS01407,BMG_DS001783,,,,,,,DOID:9119,acute myeloid leukemia,C0023467,,601626,MONDO:0018874,acute myeloid leukemia,
+BMGC_DS01408,BMG_DS001784,,,,,,,DOID:8692,myeloid leukemia,C0023470,,,MONDO:0004643,myeloid leukemia,
+BMGC_DS01409,BMG_DS001786,,,,,,,DOID:8552;DOID:0081088,"chronic myelogenous leukemia, BCR-ABL1 positive | chronic myeloid leukemia",C0023473,,,,,
+BMGC_DS01410,BMG_DS001788,,,,,,,DOID:0081082,acute myelomonocytic leukemia,C0023479,,,MONDO:0018871,acute myelomonocytic leukemia M4,
+BMGC_DS01411,BMG_DS001789,,,,,,,,,C0023480,,,MONDO:0020311,chronic myelomonocytic leukemia,
+BMGC_DS01412,BMG_DS001790,,,,,,,,,C0023481,,,MONDO:0019451,chronic neutrophilic leukemia,
+BMGC_DS01413,BMG_DS001791,,,,,,,DOID:9954,null-cell leukemia,C0023483,,,MONDO:0004932,null-cell leukemia,
+BMGC_DS01414,BMG_DS001792,,,,,,,DOID:9513,plasma cell leukemia,C0023484,,,MONDO:0018689,plasma cell leukemia,
+BMGC_DS01415,BMG_DS001793,,,,,,,DOID:1039,prolymphocytic leukemia,C0023486,,,MONDO:0001023,prolymphocytic leukemia,
+BMGC_DS01416,BMG_DS001794,,,,,,,DOID:0060318,acute promyelocytic leukemia,C0023487,,612376,MONDO:0012883,acute promyelocytic leukemia,
+BMGC_DS01417,BMG_DS001795,,,,,,,DOID:5603,T-cell acute lymphoblastic leukemia,C0023492,,,MONDO:0005525,T-cell leukemia,
+BMGC_DS01418,BMG_DS001796,,,,,,,DOID:0050523,adult T-cell leukemia/lymphoma,C0023493,,,MONDO:0019471,adult T-cell leukemia/lymphoma,
+BMGC_DS01419,BMG_DS001797,,Leukemoid Reaction,Leukemoid Reaction,,,,,,C0023501,D007955,,MONDO:0006829,leukemoid reaction,
+BMGC_DS01420,BMG_DS001798,,Leukocyte Disorders,Leukocyte Disorders,,,,DOID:9500,leukocyte disease,C0023510,D007960,,MONDO:0004805,leukocyte disorder,
+BMGC_DS01421,BMG_DS001799,267568006;154832004;191368009;191364006;142918008;111583006,Leukocytosis,Leukocytosis,,,,,,C0023518,D007964,MTHU000211,,,WBC: [other diseases] or [lymphocytosis] or [leukocytosis] | Lymphocytosis | Other WBC diseases | Leucocytosis | Leukocytosis | WBC: [other diseases] or [lymphocytosis] or [leucocytosis] | WBC: [other diseases] or [lymphocytosis] or [leucocytosis] (disorder) | Lymphocytosis | Other WBC diseases | WBC: [other diseases] or [lymphocytosis] or [leukocytosis] | WBC: [other diseases] or [lymphocytosis] or [leucocytosis] | Leukocytosis | Leucocytosis | WBC: [other diseases] or [lymphocytosis] or [leucocytosis] (disorder) | (Other white blood cell disease NOS) or (leukocytosis) | Other white blood cell disease NOS | Leucocytosis | Leukocytosis | (Other white blood cell disease NOS) or (leucocytosis) | (Other white blood cell disease NOS) or (leucocytosis) (disorder) | (Other white blood cell disease) or (leukocytosis) | Leukocytosis | Other white blood cell disease | Leucocytosis | (Other white blood cell disease) or (leucocytosis) | (Other white blood cell disease) or (leucocytosis) (disorder) | Leucocytosis | Leukocytosis | Leucocytosis (finding) | Leukocytosis | Leucocytosis | Leukocytosis (disorder)
+BMGC_DS01422,BMG_DS001800,5101009;192781003,Leukodystrophy,,,,,DOID:10579,leukodystrophy,C0023520,,MTHU037739,MONDO:0019046,leukodystrophy,Leukodystrophy | Leukodystrophy (disorder) | Leucodystrophy | Leukodystrophy | Leukodystrophy (disorder)
+BMGC_DS01423,BMG_DS001801,,,,,,,DOID:10587,Krabbe disease,C0023521,,245200,MONDO:0009499,Krabbe disease,
+BMGC_DS01424,BMG_DS001802,,"Leukodystrophy, Metachromatic","Leukodystrophy, Metachromatic",,,,DOID:10581,metachromatic leukodystrophy,C0023522,D007966,,MONDO:0018868,metachromatic leukodystrophy,
+BMGC_DS01425,BMG_DS001803,67795000,Oral leukoedema,,,,,DOID:4557,oral leukoedema,C0023523,,,MONDO:0006880,oral leukoedema,Leukoedema of mouth | Leukedema of mouth | Oral leukoedema | Leukedema of mouth (disorder)
+BMGC_DS01426,BMG_DS001804,,"Leukoencephalopathy, Progressive Multifocal","Leukoencephalopathy, Progressive Multifocal",,,,DOID:643,progressive multifocal leukoencephalopathy,C0023524,D007968,,MONDO:0016318,progressive multifocal leukoencephalopathy,
+BMGC_DS01427,BMG_DS001806,,"Leukomalacia, Periventricular","Leukomalacia, Periventricular",,,,DOID:13088,periventricular leukomalacia,C0023529,D007969,,MONDO:0015742,periventricular leukomalacia,
+BMGC_DS01428,BMG_DS001807,142917003;84828003;191348003,Leukopenia,Leukopenia,,,D72.819,DOID:615,leukopenia,C0023530,D007970,MTHU036911,MONDO:0003785,leukopenia,Leukopenia | Leucopenia | Leucopenia (finding) | Leukopenia | Leucopenia | Leukopenia (disorder) | Leukocytopenia | Leucocytopenia | Leucopenia | Leukopenia | Leucopenia (disorder)
+BMGC_DS01429,BMG_DS001808,,,,,,,,,C0023531,,,MONDO:0043243,leukoplakia,
+BMGC_DS01430,BMG_DS001809,,,,,,,,,C0023532,,,MONDO:0004844,oral mucosa leukoplakia,
+BMGC_DS01431,BMG_DS001810,,,,,,,DOID:3766,leukorrhea,C0023533,,,MONDO:0002769,leukorrhea,
+BMGC_DS01432,BMG_DS001813,,,,,,,DOID:2696,Leydig cell tumor,C0023601,,,MONDO:0006266,Leydig cell tumor,
+BMGC_DS01433,BMG_DS001814,,,,,,,DOID:8574,lichen disease,C0023643,,,MONDO:0006570,lichen disease,
+BMGC_DS01434,BMG_DS001815,64540004,Lichen planus follicularis,,,,,,,C0023645,C535892,,MONDO:0018879,lichen planopilaris,Lichen planopilaris | Lichen planus follicularis | Lichen planopilaris (disorder)
+BMGC_DS01435,BMG_DS001816,,Lichen Planus,Lichen Planus,,,,DOID:9201,lichen planus,C0023646,D008010,,MONDO:0006572,lichen planus,
+BMGC_DS01436,BMG_DS001824,,,,,,,DOID:4023,linitis plastica,C0023743,,,,,
+BMGC_DS01437,BMG_DS001825,,Lip Diseases,Lip Diseases,,,,DOID:9297,lip disease,C0023760,D008047,,MONDO:0004748,lip disorder,
+BMGC_DS01438,BMG_DS001827,,"Lipid Metabolism, Inborn Errors","Lipid Metabolism, Inborn Errors",,,,DOID:3146,lipid metabolism disorder,C0023772,D008052,,,,
+BMGC_DS01439,BMG_DS001828,,Mucopolysaccharidosis I,Mucopolysaccharidosis I,,,,DOID:12802,mucopolysaccharidosis I,C0023786,D008059,,MONDO:0001586,mucopolysaccharidosis type 1,
+BMGC_DS01440,BMG_DS001829,71325002;190789006,Lipodystrophy,Lipodystrophy,,,,DOID:811,lipodystrophy,C0023787,D008060,MTHU037286,MONDO:0006573,lipodystrophy,Lipodystrophy | Dystrophy of fatty tissue | Lipodystrophy (disorder) | (Lipodystrophy) or (Barraquer - Simons disease) | Barraquer-Simons disease | Lipodystrophy | Barraquer - Simons disease | (Lipodystrophy) or (Barraquer - Simons disease) (disorder)
+BMGC_DS01441,BMG_DS001830,,Whipple Disease,Whipple Disease,,,,DOID:8476,Whipple disease,C0023788,D008061,,MONDO:0005116,Whipple disease,
+BMGC_DS01442,BMG_DS001831,11455007,Lipoidosis,Lipidoses,,,,DOID:9455,lipid storage disease,C0023794,D008064,,MONDO:0019245,lysosomal lipid storage disorder,Lipoidosis | Lipoidosis (disorder)
+BMGC_DS01443,BMG_DS001832,,Lipoid Proteinosis of Urbach and Wiethe,Lipoid Proteinosis of Urbach and Wiethe,,,,DOID:14498,lipoid proteinosis,C0023795,D008065,247100,MONDO:0009530,lipoid proteinosis,
+BMGC_DS01444,BMG_DS001833,,,,,,,DOID:3315,lipoma,C0023798,,,MONDO:0005106,lipoma,
+BMGC_DS01445,BMG_DS001834,37095002;402693001,Lipomatosis,Lipomatosis,,,,DOID:3153,lipomatosis,C0023801,D008068,,MONDO:0006574,lipomatosis,Lipomatosis | Lipomatosis (morphologic abnormality) | Lipomatosis (disorder) | Lipomatosis
+BMGC_DS01446,BMG_DS001836,,"Lipomatosis, Multiple Symmetrical","Lipomatosis, Multiple Symmetrical",,,,DOID:14116,multiple symmetric lipomatosis,C0023804,D008069,151800,MONDO:0007908,multiple symmetric lipomatosis,
+BMGC_DS01447,BMG_DS001837,723675006,Lipomucopolysaccharidosis,Mucolipidoses,,,,,,C0023806,D009081,,MONDO:0019346,sialidosis type 1,Sialidosis type 1 (disorder) | Sialidosis type 1 | Cherry red spot myoclonus syndrome | Lipomucopolysaccharidosis | Normomorphic sialidosis
+BMGC_DS01448,BMG_DS001838,,Hyperlipoproteinemia Type I,Hyperlipoproteinemia Type I,,,,DOID:14118,familial lipoprotein lipase deficiency,C0023817,D008072,238600,MONDO:0009387,familial lipoprotein lipase deficiency,
+BMGC_DS01449,BMG_DS001839,,,,,,,DOID:3382,liposarcoma,C0023827,,,MONDO:0005060,liposarcoma,
+BMGC_DS01450,BMG_DS001840,186315001;4241002,Listeriosis,Listeriosis,,,A32,DOID:11573,listeriosis,C0023860,D008088,,MONDO:0005828,listeriosis,Listeriosis | Listeriosis (disorder) | Listeriosis | Infection due to Listeria monocytogenes | Circling disease | Listerellosis | Listeriosis (disorder) | Listeria monocytogenes infection
+BMGC_DS01451,BMG_DS001841,,Little's Disease,Cerebral Palsy,,,,DOID:10965,spastic diplegia,C0023882,D002547,,,,
+BMGC_DS01452,BMG_DS001842,,Liver Abscess,Liver Abscess,,,,,,C0023885,D008100,,,,
+BMGC_DS01453,BMG_DS001843,,"Liver Abscess, Amebic","Liver Abscess, Amebic",,,,,,C0023886,D008101,,,,
+BMGC_DS01454,BMG_DS001844,,Liver Cirrhosis,Liver Cirrhosis,,,,DOID:5082,liver cirrhosis,C0023890,D008103,,MONDO:0005155,cirrhosis of liver,
+BMGC_DS01455,BMG_DS001845,,"Liver Cirrhosis, Alcoholic","Liver Cirrhosis, Alcoholic",,,,DOID:14018,alcoholic liver cirrhosis,C0023891,D008104,,MONDO:0006644,alcoholic liver cirrhosis,
+BMGC_DS01456,BMG_DS001846,1761006,Biliary cirrhosis,,,,,DOID:12236,primary biliary cholangitis,C0023892,,MTHU037261,,,Biliary cirrhosis | Cholangitic cirrhosis | Cholestatic cirrhosis | Chronic nonsuppurative destructive cholangitis | Biliary cirrhosis (disorder)
+BMGC_DS01457,BMG_DS001847,,,,,,,DOID:409,liver disease,C0023895,,,,,
+BMGC_DS01458,BMG_DS001848,,Alcoholic Liver Diseases,"Liver Diseases, Alcoholic",,,,,,C0023896,D008108,,MONDO:0043693,alcoholic liver diseases,
+BMGC_DS01459,BMG_DS001849,,"Liver Diseases, Parasitic","Liver Diseases, Parasitic",,,,,,C0023897,D008109,,,,
+BMGC_DS01460,BMG_DS001850,,,,,,,DOID:3571,liver cancer,C0023903,,,,,
+BMGC_DS01461,BMG_DS001851,,Lobstein Disease,Osteogenesis Imperfecta,,,,DOID:0110334,osteogenesis imperfecta type 1,C0023931,D010013,166200,MONDO:0008146,osteogenesis imperfecta type 1,
+BMGC_DS01462,BMG_DS001853,,Locked-In Syndrome,Locked-In Syndrome,,,,DOID:12697,locked-in syndrome,C0023944,D000080422,,MONDO:0016567,locked-in syndrome,
+BMGC_DS01463,BMG_DS001854,,,,,,,DOID:13523,loiasis,C0023968,,,MONDO:0016566,loiasis,
+BMGC_DS01464,BMG_DS001855,,,,,,,DOID:2843,long QT syndrome,C0023976,,,MONDO:0002442,long QT syndrome,
+BMGC_DS01465,BMG_DS001856,,,,,,,DOID:10250,louping ill,C0024025,,,,,
+BMGC_DS01466,BMG_DS001857,,,,,,,DOID:13087,Lown-Ganong-Levine syndrome,C0024054,,,,,
+BMGC_DS01467,BMG_DS001858,,,,,,,DOID:4558,Ludwig's angina,C0024081,,,MONDO:0006576,Ludwig's angina,
+BMGC_DS01468,BMG_DS001860,,,,,,,DOID:0060317,lung abscess,C0024110,,,MONDO:0000744,lung abscess,
+BMGC_DS01469,BMG_DS001861,266374002,Lung diseases,,,,,DOID:850,lung disease,C0024115,,,MONDO:0005275,lung disorder,Respiratory system diseases (& lung diseases) | Respiratory diseases | Respiratory system diseases | Lung diseases | Respiratory system diseases (& lung diseases) (disorder)
+BMGC_DS01470,BMG_DS001862,,"Lung Diseases, Fungal","Lung Diseases, Fungal",,,,,,C0024116,D008172,,MONDO:0005766,fungal lung infectious disease,
+BMGC_DS01471,BMG_DS001863,,Chronic Obstructive Airway Disease,"Pulmonary Disease, Chronic Obstructive",,,,DOID:3083,chronic obstructive pulmonary disease,C0024117,D029424,606963,MONDO:0005002,chronic obstructive pulmonary disease,
+BMGC_DS01472,BMG_DS001864,,"Lung Diseases, Parasitic","Lung Diseases, Parasitic",,,,,,C0024118,D008174,,,,
+BMGC_DS01473,BMG_DS001865,,,,,,,DOID:3683,lung benign neoplasm,C0024121,,,MONDO:0021117,lung neoplasm,
+BMGC_DS01474,BMG_DS001867,,"Lupus Erythematosus, Cutaneous","Lupus Erythematosus, Cutaneous",,,,,,C0024137,D008178,,MONDO:0005282;MONDO:0018887,cutaneous lupus erythematosus | obsolete rare cutaneous lupus erythematosus,
+BMGC_DS01475,BMG_DS001868,13902000;238927000,Chronic discoid lupus erythematosus,,,,,,,C0024138,,,,,Discoid lupus erythematosus | Discoid lupus erythematosus (disorder) | CDLE - Chronic discoid lupus erythematosus | Chronic discoid lupus erythematosus | Chronic discoid lupus erythematosus (disorder)
+BMGC_DS01476,BMG_DS001869,,"Lupus Erythematosus, Subacute Cutaneous","Lupus Erythematosus, Cutaneous",,,,,,C0024140,D008178,,MONDO:0015573;MONDO:0018887,obsolete rare cutaneous lupus erythematosus | subacute cutaneous lupus erythematosus,
+BMGC_DS01477,BMG_DS001870,,"Lupus Erythematosus, Systemic","Lupus Erythematosus, Systemic",,,,DOID:9074,systemic lupus erythematosus,C0024141,D008180,152700,MONDO:0007915,systemic lupus erythematosus,
+BMGC_DS01478,BMG_DS001871,,Lupus Nephritis,Lupus Nephritis,,,,DOID:0080162,lupus nephritis,C0024143,D008181,,MONDO:0005556,lupus nephritis,
+BMGC_DS01479,BMG_DS001872,,Chilblain lupus 1,,,,,DOID:0060386,Chilblain lupus,C0024145,C535924,610448,MONDO:0012500,chilblain lupus 1,
+BMGC_DS01480,BMG_DS001873,,Lutembacher Syndrome,Lutembacher Syndrome,,,,DOID:1998,Lutembacher's syndrome,C0024164,D008185,,MONDO:0006839,Lutembacher syndrome,
+BMGC_DS01481,BMG_DS001874,,Lyme Disease,Lyme Disease,,,,DOID:11729,Lyme disease,C0024198,D008193,,MONDO:0019632,Lyme disease,
+BMGC_DS01482,BMG_DS001875,19471005,Lymphadenitis,Lymphadenitis,BD90.2Z,"Chronic lymphadenitis, unspecified",I88.1,DOID:1602,lymphadenitis,C0024205,D008199,MTHU037495,MONDO:0002052,lymphadenitis,Lymphadenitis | Adenitis | Inflammation of lymph node | Lymphadenitis (disorder)
+BMGC_DS01483,BMG_DS001876,48087001,Lymphangiectasis,Lymphangiectasis,BD93.Z,"Lymphoedema, unspecified",I89.0,,,C0024214,D008200,,MONDO:0006840,lymphangiectasis,Lymphangiectasis | Lymphangiectasia | Lymphangiectasis (morphologic abnormality)
+BMGC_DS01484,BMG_DS001879,,,,,,,DOID:1475,lymphangioma,C0024221,,,MONDO:0002013,lymphangioma,
+BMGC_DS01485,BMG_DS001882,1415005,Lymphangitis,Lymphangitis,BD91,Lymphangitis,I89.1,DOID:9317,lymphangitis,C0024225,D008205,MTHU075696,MONDO:0005832,lymphangitis,Lymphangitis | Lymphangitis (disorder) | Inflammation of lymphatics
+BMGC_DS01486,BMG_DS001883,,Lymphatic Diseases,Lymphatic Diseases,,,,DOID:75,lymphatic system disease,C0024228,D008206,,MONDO:0044986,lymphoid system disorder,
+BMGC_DS01487,BMG_DS001884,155485008;30213001;234097001;195486001;266334008,Lymphedema,Lymphedema,,,,DOID:4977,lymphedema,C0024236,D008209,MTHU001042,MONDO:0019297,lymphedema,(Elephantiasis) or (lymphoedema [& NOS]) | (Elephantiasis) or (lymphedema [& NOS]) | Elephantiasis | Lymphoedema NOS | Lymphoedema | Lymphedema | Lymphedema NOS | (Elephantiasis) or (lymphoedema [& NOS]) (disorder) | Lymphatic edema | Acquired lymphedema | Lymphedema | Acquired lymphoedema | Lymphatic oedema | Lymphoedema | Lymphatic edema (morphologic abnormality) | Lymphatic oedema | Lymphoedema | Lymphatic edema | Lymphedema | Lymphedema (disorder) | Lymphedema | (Noninfective lymphatic disorders) or (lymphoedema) | Lymphoedema | (Noninfective lymphatic disorders) or (lymphedema) | Noninfective lymphatic disorders | (Noninfective lymphatic disorders) or (lymphoedema) (disorder) | Elephantiasis | Lymphoedema | Lymphoedema NOS | (Elephantiasis) or (lymphoedema [& NOS]) | Lymphedema | Lymphedema NOS | (Elephantiasis) or (lymphedema [& NOS]) | (Elephantiasis) or (lymphoedema [& NOS]) (disorder)
+BMGC_DS01488,BMG_DS001885,234109007,Lymphocele,Lymphocele,,,,DOID:4347,lymphocele,C0024248,D008210,,MONDO:0002968,lymphocele,Lymphocele | Lymphocele (disorder)
+BMGC_DS01489,BMG_DS001886,,Lymphocytic Choriomeningitis,Lymphocytic Choriomeningitis,,,,DOID:12155,lymphocytic choriomeningitis,C0024266,D008216,,MONDO:0001449,lymphocytic choriomeningitis,
+BMGC_DS01490,BMG_DS001887,67023009;154832004;267568006,Lymphocytosis,Lymphocytosis,,,,,,C0024282,D008218,,,,Lymphocytosis | Lymphocytosis (disorder) | Lymphocytosis | Other WBC diseases | WBC: [other diseases] or [lymphocytosis] or [leukocytosis] | WBC: [other diseases] or [lymphocytosis] or [leucocytosis] | Leukocytosis | Leucocytosis | WBC: [other diseases] or [lymphocytosis] or [leucocytosis] (disorder) | WBC: [other diseases] or [lymphocytosis] or [leukocytosis] | Lymphocytosis | Other WBC diseases | Leucocytosis | Leukocytosis | WBC: [other diseases] or [lymphocytosis] or [leucocytosis] | WBC: [other diseases] or [lymphocytosis] or [leucocytosis] (disorder)
+BMGC_DS01491,BMG_DS001888,,Lymphogranuloma Venereum,Lymphogranuloma Venereum,,,,DOID:13819,lymphogranuloma venereum,C0024286,D008219,,MONDO:0005834,lymphogranuloma venereum,
+BMGC_DS01492,BMG_DS001889,,"Lymphohistiocytosis, Hemophagocytic","Lymphohistiocytosis, Hemophagocytic",,,,DOID:0050120,hemophagocytic lymphohistiocytosis,C0024291,D051359,,,,
+BMGC_DS01493,BMG_DS001890,,,,,,,DOID:0060058,lymphoma,C0024299,,,MONDO:0005062,lymphoma,
+BMGC_DS01494,BMG_DS001891,,,,,,,,,C0024301,,,MONDO:0018906,follicular lymphoma,
+BMGC_DS01495,BMG_DS001892,,,,,,,DOID:8538,reticulosarcoma,C0024302,,267730,MONDO:0009975,reticulum cell sarcoma,
+BMGC_DS01496,BMG_DS001893,,,,,,,DOID:0060060,non-Hodgkin lymphoma,C0024305,,,MONDO:0018908,non-Hodgkin lymphoma,
+BMGC_DS01497,BMG_DS001894,,,,,,,DOID:0081307,lymphomatoid granulomatosis,C0024307,,,MONDO:0019466,lymphomatoid granulomatosis,
+BMGC_DS01498,BMG_DS001895,48813009,Lymphopenia,Lymphopenia,,,,DOID:614,lymphopenia,C0024312,D008231,MTHU006263,MONDO:0003783,lymphopenia,Lymphocytopenia | Lymphopenia | Alymphocytosis | Lymphocytopenia (disorder)
+BMGC_DS01499,BMG_DS001896,,,,,,,,,C0024314,,,MONDO:0016537,lymphoproliferative syndrome,
+BMGC_DS01500,BMG_DS001897,,Machado-Joseph Disease,Machado-Joseph Disease,,,,DOID:1440,Machado-Joseph disease,C0024408,D017827,109150,MONDO:0007182,Machado-Joseph disease,
+BMGC_DS01501,BMG_DS001898,,,,,,,DOID:0060901,lymphoplasmacytic lymphoma,C0024419,,,MONDO:0100280,Waldenstrom macroglobulinemia,
+BMGC_DS01502,BMG_DS001899,25273001;52106009;204628000,Macroglossia,Macroglossia,,,,,,C0024421,D008260,MTHU000268,MONDO:0015496,macroglossia,Enlargement of tongue | Enlargement of tongue (disorder) | Macroglossia | Large tongue | Congenital hypertrophy of tongue | Enlarged tongue | Acquired hypertrophy of tongue | Congenital macroglossia | Enlargement of tongue | Acquired macroglossia | Hypertrophy of tongue | Large tongue | Enlarged tongue (disorder) | Macroglossia | Congenital hypertrophy of tongue | Congenital tongue hypertrophy | (Congenital): [macroglossia (& acquired)] or [tongue hypertrophy] | (Congenital): [macroglossia (& acquired)] or [tongue hypertrophy] (disorder)
+BMGC_DS01503,BMG_DS001900,302891003,Macular degeneration,,,,,DOID:4448,macular degeneration,C0024437,,MTHU003281,MONDO:0003004,macular degeneration,Macular degeneration | Senile macular retinal degeneration | Macular degeneration (disorder)
+BMGC_DS01504,BMG_DS001901,60258001,Macular corneal dystrophy,,,,H18.55,DOID:2565,macular corneal dystrophy,C0024439,,MTHU037954,,,Macular corneal dystrophy | Macular corneal dystrophy (disorder)
+BMGC_DS01505,BMG_DS001902,,"Macular Edema, Cystoid",Macular Edema,,,,DOID:4447,cystoid macular edema,C0024440,D008269,153880,MONDO:0007935,cystoid macular edema,
+BMGC_DS01506,BMG_DS001903,,Macular Holes,Retinal Perforations,,,,DOID:7633,macular holes,C0024441,D012167,,MONDO:0006843,macular holes,
+BMGC_DS01507,BMG_DS001904,410039003,Mycetoma,Mycetoma,,,B47,DOID:13078,eumycotic mycetoma,C0024449,D008271,,MONDO:0016823,mycetoma,Mycetoma (disorder) | Mycetoma | Mycetomata
+BMGC_DS01508,BMG_DS001905,,Maffucci Syndrome,Enchondromatosis,,,,DOID:4624,Ollier disease,C0024454,D004687,614569,MONDO:0013808,Maffucci syndrome,
+BMGC_DS01509,BMG_DS001906,,Magnesium Deficiency,Magnesium Deficiency,,,,,,C0024473,D008275,,MONDO:0006844,magnesium deficiency,
+BMGC_DS01510,BMG_DS001907,,Majewski Syndrome,Short Rib-Polydactyly Syndrome,,,,,,C0024507,D012779,263520,MONDO:0009894,short-rib thoracic dysplasia 6 with or without polydactyly,
+BMGC_DS01511,BMG_DS001908,,,,,,,DOID:1470,major depressive disorder,C0024517,,,,,
+BMGC_DS01512,BMG_DS001909,,Malabsorption Syndrome,Malabsorption Syndromes,,,,,,C0024523,D008286,,MONDO:0020598,malabsorption syndrome,
+BMGC_DS01513,BMG_DS001911,154374002;61462000,Malaria,Malaria,,,,DOID:12365,malaria,C0024530,D008288,,MONDO:0005136,malaria,Malaria | Malaria (disorder) | Malaria | Paludism | Plasmodiosis | Malaria (disorder)
+BMGC_DS01514,BMG_DS001913,,"Malaria, Cerebral","Malaria, Cerebral",,,,DOID:14069,cerebral malaria,C0024534,D016779,,MONDO:0005625,cerebral malaria,
+BMGC_DS01515,BMG_DS001914,,"Malaria, Falciparum","Malaria, Falciparum",,,,DOID:14067,Plasmodium falciparum malaria,C0024535,D016778,,MONDO:0005920,Plasmodium falciparum malaria,
+BMGC_DS01516,BMG_DS001915,27618009,Quartan malaria,,,,,DOID:14324,Plasmodium malariae malaria,C0024536,,,MONDO:0001943,Plasmodium malariae malaria,Quartan malaria | Malaria by Plasmodium malariae | Malariae malaria | Quartan malaria (disorder)
+BMGC_DS01517,BMG_DS001916,,"Malaria, Vivax","Malaria, Vivax",,,,DOID:12978,Plasmodium vivax malaria,C0024537,D016780,,MONDO:0005921,Plasmodium vivax malaria,
+BMGC_DS01518,BMG_DS001917,,Malignant Carcinoid Syndrome,Malignant Carcinoid Syndrome,,,,,,C0024586,D008303,,MONDO:0100347,carcinoid syndrome,
+BMGC_DS01519,BMG_DS001918,78975002,Malignant essential hypertension,,,,,DOID:10823,malignant essential hypertension,C0024588,,,MONDO:0001133,malignant essential hypertension,Malignant essential hypertension | Accelerated essential hypertension | Malignant essential hypertension (disorder)
+BMGC_DS01520,BMG_DS001919,,,,,,,DOID:8545,malignant hyperthermia,C0024591,,,MONDO:0018493,malignant hyperthermia of anesthesia,
+BMGC_DS01521,BMG_DS001920,,,,,,,DOID:3571,liver cancer,C0024620,,,,,
+BMGC_DS01522,BMG_DS001922,,,,,,,DOID:4645,retinal cancer,C0024622,,,MONDO:0003072,retinal cancer,
+BMGC_DS01523,BMG_DS001923,,,,,,,DOID:10534,stomach cancer,C0024623,,613659,MONDO:0001056,gastric cancer,
+BMGC_DS01524,BMG_DS001924,,,,,,,DOID:1324,lung cancer,C0024624,,,,,
+BMGC_DS01525,BMG_DS001926,,Mandibular Diseases,Mandibular Diseases,,,,,,C0024689,D008336,,,,
+BMGC_DS01526,BMG_DS001927,,,,,,,DOID:2338,mandibular cancer,C0024694,,,,,
+BMGC_DS01527,BMG_DS001928,128867006;67172004,Mange,Mite Infestations,,,,,,C0024709,D008924,,,,Mange | Mange (disorder) | Infestation by Sarcoptes scabiei | Sarcoptic mange | Animal scabies | Infestation by Sarcoptes scabiei (disorder)
+BMGC_DS01528,BMG_DS001929,,"Mange, Sarcoptic",Scabies,,,,,,C0024710,D012532,,,,
+BMGC_DS01529,BMG_DS001930,,,,,,,DOID:3312,bipolar disorder,C0024713,,,MONDO:0024612,manic bipolar affective disorder,
+BMGC_DS01530,BMG_DS001931,,alpha-Mannosidosis,alpha-Mannosidosis,,,,DOID:3413,alpha-mannosidosis,C0024748,D008363,248500,MONDO:0009561,alpha-mannosidosis,
+BMGC_DS01531,BMG_DS001932,240849009,Mansonelliasis,Mansonelliasis,1F66.1,Mansonelliasis,B74.4,DOID:1081,mansonelliasis,C0024759,D008368,,MONDO:0005838,mansonelliasis,Mansonelliasis | Mansonelliasis (disorder)
+BMGC_DS01532,BMG_DS001933,,Maple Syrup Urine Disease,Maple Syrup Urine Disease,,,,DOID:9269,maple syrup urine disease,C0024776,D008375,,MONDO:0009563,maple syrup urine disease,
+BMGC_DS01533,BMG_DS001934,,Marburg Virus Disease,Marburg Virus Disease,,,,DOID:4327,Marburg hemorrhagic fever,C0024788,D008379,,MONDO:0020500,Marburg hemorrhagic fever,
+BMGC_DS01534,BMG_DS001935,154805009;267559009;1963002,Paroxysmal nocturnal hemoglobinuria,,,,,DOID:0060284,paroxysmal nocturnal hemoglobinuria,C0024790,,,MONDO:0100244,paroxysmal nocturnal hemoglobinuria,Hemoglobinuria: [external cause] or [hemolytic] or [paroxysmal nocturnal] | Haemoglobinuria: [external cause] or [haemolytic] or [paroxysmal nocturnal] | Parox. noct. haemoglobinuria | Haemoglobinuria - external causation | Paroxysmal nocturnal haemoglobinuria | Haemoglobinuria-haemol. | Haemoglobinuria-external cause | Hemoglobinuria - external causation | Parox. noct. hemoglobinuria | Paroxysmal nocturnal hemoglobinuria | Hemoglobinuria-hemol. | Hemoglobinuria-external cause | Haemoglobinuria: [external cause] or [haemolytic] or [paroxysmal nocturnal] (disorder) | Hemoglobinuria: [external cause] or [hemolytic] or [paroxysmal nocturnal] | Haemoglobinuria: [external cause] or [haemolytic] or [paroxysmal nocturnal] | Hemoglobinuria - external causation | Hemoglobinuria-external cause | Hemoglobinuria-hemol. | Parox. noct. hemoglobinuria | Paroxysmal nocturnal hemoglobinuria | Paroxysmal nocturnal haemoglobinuria | Parox. noct. haemoglobinuria | Haemoglobinuria - external causation | Haemoglobinuria-external cause | Haemoglobinuria-haemol. | Haemoglobinuria: [external cause] or [haemolytic] or [paroxysmal nocturnal] (disorder) | Paroxysmal nocturnal hemoglobinuria | Marchiafava-Micheli syndrome | Paroxysmal nocturnal haemoglobinuria | Paroxysmal nocturnal hemoglobinuria (disorder) | PNH - paroxysmal nocturnal hemoglobinuria | PNH - paroxysmal nocturnal haemoglobinuria
+BMGC_DS01535,BMG_DS001936,,Marfan Syndrome,Marfan Syndrome,,,,DOID:14323,Marfan syndrome,C0024796,D008382,154700,MONDO:0007947,Marfan syndrome,
+BMGC_DS01536,BMG_DS001938,,,,,,,DOID:9505,cannabis abuse,C0024809,,,,,
+BMGC_DS01537,BMG_DS001939,80734006;190961002,Marinesco-Sjogren syndrome,,,,,,,C0024814,,248800,MONDO:0009567,Marinesco-Sjogren syndrome,Marinesco-Sjogren syndrome | Oligophrenic cerebellolenticular degeneration | Marinesco-Sjögren syndrome (disorder) | Marinesco-Sjögren syndrome | (Marinesco-Sjogren syndrome) or (disorder of metabolism NOS) | Disorder of metabolism NOS | Marinesco Sjogren syndrome | Marinesco-Sjogren syndrome | (Marinesco-Sjogren syndrome) or (disorder of metabolism NOS) (disorder)
+BMGC_DS01538,BMG_DS001940,198099006;266641007;45198002;155952005,Mastitis,Mastitis,,,,DOID:10690,mastitis,C0024894,D008413,,MONDO:0006849,mastitis,"Inflammatory breast disease (& [abscess, non puerperal] or [mastitis (& non puerperal)]) | Mastitis | Non-puerperal mastitis | Inflammatory breast disease | Abscess, breast, non puerperal | Breast abscess - non puerperal | Mastitis - non puerperal | Inflammatory breast disease (& [abscess, non puerperal] or [mastitis (& non puerperal)]) (disorder) | Inflammatory disease of breast (& [mastitis]) | Inflammatory disorder of breast | Mastitis | Inflammatory disease of breast | Inflammatory disease of breast (& [mastitis]) (disorder) | Mastitis | Mastitis (disorder) | Inflammatory disease of breast (& [mastitis]) | Mastitis | Inflammatory disorder of breast | Inflammatory disease of breast | Inflammatory disease of breast (& [mastitis]) (disorder)"
+BMGC_DS01539,BMG_DS001943,,,,,,,DOID:350,mastocytosis,C0024899,,,MONDO:0007950,mastocytosis,
+BMGC_DS01540,BMG_DS001944,,"Mastocytosis, Bullous","Mastocytosis, Cutaneous",,,,,,C0024900,D034701,,,,
+BMGC_DS01541,BMG_DS001945,,,,,,,DOID:3665,diffuse cutaneous mastocytosis,C0024901,,,MONDO:0019315,diffuse cutaneous mastocytosis,
+BMGC_DS01542,BMG_DS001946,155230007;52404001,Mastoiditis,Mastoiditis,,,,DOID:0060322,mastoiditis,C0024904,D008417,MTHU005996,MONDO:0000748,mastoiditis,Mastoiditis | Mastoiditis (disorder)
+BMGC_DS01543,BMG_DS001947,,Maxillary Diseases,Maxillary Diseases,,,,,,C0024950,D008439,,,,
+BMGC_DS01544,BMG_DS001948,,,,,,,DOID:4618,maxillary cancer,C0024954,,,MONDO:0005841,maxillary neoplasm,
+BMGC_DS01545,BMG_DS001949,,,,,,,DOID:1358,maxillary sinus benign neoplasm,C0024958,,,MONDO:0006850,maxillary sinus neoplasm,
+BMGC_DS01546,BMG_DS001950,,Maxillary Sinusitis,Maxillary Sinusitis,,,,DOID:2051,maxillary sinusitis,C0024959,D015523,,MONDO:0005842,maxillary sinusitis,
+BMGC_DS01547,BMG_DS001951,14189004;154338006,Measles,Measles,,,B05,DOID:8622,measles,C0025007,D008457,,MONDO:0004619,measles,Measles | Rubeola | Morbilli | Measles (disorder) | Measles | Measles (disorder)
+BMGC_DS01548,BMG_DS001952,,,,,,,DOID:9487,Meckel's diverticulum,C0025037,,155140,MONDO:0007955,Meckel diverticulum,
+BMGC_DS01549,BMG_DS001953,,Meconium Aspiration Syndrome,Meconium Aspiration Syndrome,,,,DOID:11049,meconium aspiration syndrome,C0025048,D008471,,MONDO:0006851,meconium aspiration syndrome,
+BMGC_DS01550,BMG_DS001956,,Mediastinal Emphysema,Mediastinal Emphysema,,,,,,C0025062,D008478,,,,
+BMGC_DS01551,BMG_DS001957,,,,,,,DOID:5559,mediastinal cancer,C0025063,,,MONDO:0021386,neoplasm of mediastinum,
+BMGC_DS01552,BMG_DS001958,373409004;47597000,Mediastinitis,Mediastinitis,,,J98.51,DOID:819,mediastinitis,C0025064,D008480,,MONDO:0004492,mediastinitis,Inflammatory disorder of mediastinum (disorder) | Inflammatory disorder of mediastinum | Mediastinitis | Mediastinitis | Mediastinitis (disorder)
+BMGC_DS01553,BMG_DS001959,,,,,,,DOID:0050902,medulloblastoma,C0025149,,155255,MONDO:0007959,medulloblastoma,
+BMGC_DS01554,BMG_DS001960,,,,,,,DOID:11372,megacolon,C0025160,,,MONDO:0001273,megacolon,
+BMGC_DS01555,BMG_DS001961,,"Megacolon, Toxic","Megacolon, Toxic",,,,DOID:1770,toxic megacolon,C0025162,D008532,,MONDO:0002105,toxic megacolon,
+BMGC_DS01556,BMG_DS001962,70667005,Megaesophagus,Esophageal Achalasia,,,,DOID:13186,megaesophagus,C0025164,D004931,,MONDO:0001656,megaesophagus,Megaesophagus | Megaoesophagus | Megaesophagus (disorder)
+BMGC_DS01557,BMG_DS001963,,Meige Syndrome,Meige Syndrome,,,,DOID:3982,Meige syndrome,C0025183,D008538,,MONDO:0019772,blepharospasm-oromandibular dystonia syndrome,
+BMGC_DS01558,BMG_DS001965,,,,,,,,,C0025193,,,MONDO:0002444,melancholia,
+BMGC_DS01559,BMG_DS001966,,,,,,,DOID:1909,melanoma,C0025202,,,MONDO:0005105,melanoma,
+BMGC_DS01560,BMG_DS001967,267870007;156438005;48010006;414662006,Melanosis,Melanosis,,,,,,C0025209,D008548,,,,Lentigo | Freckles | Dyschromia NOS | Melanosis | (Dyschromia NOS) or (freckles) or (lentigo) or (melanosis) | (Dyschromia NOS) or (freckles) or (lentigo) or (melanosis) (disorder) | Dyschromia NOS | Freckles | Melanosis | Lentigo | (Dyschromia NOS) or (freckles) or (lentigo) or (melanosis) | (Dyschromia NOS) or (freckles) or (lentigo) or (melanosis) (disorder) | Melanosis | Melanosis (morphologic abnormality) | Melanosis (disorder) | Melanosis
+BMGC_DS01561,BMG_DS001969,36209000,Chloasma,Melanosis,ED60.1,Melasma,L81.1,,,C0025218,D008548,,,,Chloasma | Melasma | Chloasma (disorder)
+BMGC_DS01562,BMG_DS001970,,Meleda Disease,"Keratoderma, Palmoplantar",,,,,,C0025221,D007645,248300,MONDO:0009552,mal de Meleda,
+BMGC_DS01563,BMG_DS001971,428111003;34458001,Melioidosis,Melioidosis,,,,DOID:5052,melioidosis,C0025229,D008554,,MONDO:0017775,melioidosis,Melioidosis (disorder) | Infection due to Burkholderia pseudomallei | Infection due to Whitmore's bacillus | Infection due to Pseudomonas pseudomallei | Melioidosis | Whitmore's disease | Infection due to Malleomyces pseudomallei | Pseudoglanders | Melioidosis | Infection due to Pseudomonas pseudomallei | Infection due to Malleomyces pseudomallei | Infection due to Whitmore's bacillus | Whitmore's disease | Pseudoglanders (disorder)
+BMGC_DS01564,BMG_DS001972,,Melkersson-Rosenthal Syndrome,Melkersson-Rosenthal Syndrome,,,,DOID:1761,Melkersson-Rosenthal syndrome,C0025235,D008556,155900,MONDO:0007969,Melkersson-Rosenthal syndrome,
+BMGC_DS01565,BMG_DS001973,,Melnick-Needles Syndrome,Osteochondrodysplasias,,,,DOID:0111788,Melnick-Needles syndrome,C0025237,D010009,309350,MONDO:0010650,Melnick-Needles syndrome,
+BMGC_DS01566,BMG_DS001974,240173003;44697002,Melorheostosis,Melorheostosis,,,,DOID:4253,melorheostosis,C0025239,D008557,MTHU041350,,,Melorheostosis | Melorheostosis (disorder) | Melorheostosis | Rheostosis | Leri's disease | Candle wax disease | Flowing hyperostosis | Osteopathia hyperostotica congenita | Melorheostosis (disorder)
+BMGC_DS01567,BMG_DS001975,,,,,,,DOID:10017,multiple endocrine neoplasia type 1,C0025267,,131100,MONDO:0007540,multiple endocrine neoplasia type 1,
+BMGC_DS01568,BMG_DS001976,,,,,,,DOID:0050430,multiple endocrine neoplasia type 2A,C0025268,,171400,MONDO:0008234,multiple endocrine neoplasia type 2A,
+BMGC_DS01569,BMG_DS001977,,,,,,,DOID:10016,multiple endocrine neoplasia type 2B,C0025269,,162300,MONDO:0008082,multiple endocrine neoplasia type 2B,
+BMGC_DS01570,BMG_DS001978,,Meniere Disease,Meniere Disease,,,,DOID:9849,Meniere's disease,C0025281,D008575,156000,MONDO:0007972,Meniere disease,
+BMGC_DS01571,BMG_DS001979,,,,,,,,,C0025284,,,MONDO:0016743,tumor of meninges,
+BMGC_DS01572,BMG_DS001980,,,,,,,DOID:3565,meningioma,C0025286,,,MONDO:0016642,meningioma,
+BMGC_DS01573,BMG_DS001981,7180009;154983000,Meningitis,Meningitis,,,,DOID:9471,meningitis,C0025289,D008581,MTHU005994,MONDO:0021108,meningitis,Meningitis | Meningitis (disorder)
+BMGC_DS01574,BMG_DS001982,,Aseptic Meningitis,"Meningitis, Aseptic",,,,DOID:12157,aseptic meningitis,C0025290,D008582,,MONDO:0006662,aseptic meningitis,
+BMGC_DS01575,BMG_DS001983,,"Meningitis, Haemophilus","Meningitis, Haemophilus",,,,DOID:0080179,haemophilus meningitis,C0025292,D008583,,MONDO:0000889,haemophilus meningitis,
+BMGC_DS01576,BMG_DS001984,,"Meningitis, Listeria","Meningitis, Listeria",,,,DOID:11572,Listeria meningitis,C0025293,D008584,,MONDO:0006836,Listeria meningitis,
+BMGC_DS01577,BMG_DS001985,154307005;28476005;186363003;192644005,Meningococcal meningitis,,1C1C.0,Meningococcal meningitis,A39.0,,,C0025294,,,MONDO:0018059,meningococcal meningitis,Meningococcal meningitis | Meningococcal meningitis (disorder) | Epidemic meningitis | Cerebrospinal meningitis | Meningococcal meningitis | Meningococcal meningitis (disorder) | Meningococcal cerebrospinal fever
+BMGC_DS01578,BMG_DS001986,,"Meningitis, Pneumococcal","Meningitis, Pneumococcal",,,,,,C0025295,D008586,,MONDO:0006913,pneumococcal meningitis,
+BMGC_DS01579,BMG_DS001987,154321007;266190006;154984006;267680008;154985007;58170007,Viral meningitis,,,,A87,DOID:10310,viral meningitis,C0025297,,,MONDO:0007015,viral meningitis,"Other CNS viral disease | Other central nervous system viral disease | Viral encephalitis | Encephalitis - viral | Viral meningitis | Meningitis - viral NOS | Viral: [other CNS disease] or [encephalitis] or [meningitis (& [NOS])] | Viral: [other CNS disease] or [encephalitis] or [meningitis (& [NOS])] (disorder) | Viral: [other CNS disease] or [encephalitis] or [meningitis (& [NOS])] | Other CNS viral disease | Encephalitis - viral | Viral encephalitis | Meningitis - viral NOS | Viral meningitis | Other central nervous system viral disease | Viral: [other CNS disease] or [encephalitis] or [meningitis (& [NOS])] (disorder) | Meningitis: [bacterial] or [viral] | Bacterial meningitis | Viral meningitis | Meningitis: [bacterial] or [viral] (disorder) | Viral meningitis | Bacterial meningitis | Meningitis: [bacterial] or [viral] | Meningitis: [bacterial] or [viral] (disorder) | Viral meningitis | Viral meningitis (disorder) | Viral meningitis | Aseptic meningitis, viral | Abacterial meningitis | Viral meningitis (disorder) | Meningitis, viral"
+BMGC_DS01580,BMG_DS001988,32941003;268308005;156890007;171131006,Meningocele,,,,,DOID:1088,meningocele,C0025299,,MTHU049652,MONDO:0001147,meningocele,Congenital meningocele | Congenital meningocele (disorder) | (Spina bifida - no hydrocephalus) or (meningocele) or (myelocele) | Meningocele | Myelocele | Spina bifida -no hydrocephalus | (Spina bifida - no hydrocephalus) or (meningocele) or (myelocele) (disorder) | Spina bifida -no hydrocephalus | Meningocele | Myelocele | (Spina bifida - no hydrocephalus) or (meningocele) or (myelocele) | (Spina bifida - no hydrocephalus) or (meningocele) or (myelocele) (disorder) | Meningocele | Meningocele (disorder)
+BMGC_DS01581,BMG_DS001989,,Meningococcal Infections,Meningococcal Infections,,,,,,C0025303,D008589,,MONDO:0005373,meningococcal infection,
+BMGC_DS01582,BMG_DS001990,,Meningococcal Septicemia,Meningococcal Infections,,,,,,C0025306,D008589,,MONDO:0042972,meningococcemia,
+BMGC_DS01583,BMG_DS001991,7125002,Meningoencephalitis,Meningoencephalitis,,,A69.22,DOID:10554,meningoencephalitis,C0025309,D008590,MTHU037268,MONDO:0005845,meningoencephalitis,Meningoencephalitis | Meningoencephalitis (disorder)
+BMGC_DS01584,BMG_DS001994,,,,,,,DOID:0060326,myelomeningocele,C0025312,,,MONDO:0019773,myelomeningocele,
+BMGC_DS01585,BMG_DS001995,123756000,Menopausal syndrome,,,,,,,C0025319,,,,,Menopausal syndrome | Menopausal syndrome (disorder)
+BMGC_DS01586,BMG_DS001996,,Premature Menopause,"Menopause, Premature",,,,DOID:10787,premature menopause,C0025322,D008594,,MONDO:0001119,premature menopause,
+BMGC_DS01587,BMG_DS001997,,"Menstruation, Retrograde",Menstruation Disturbances,,,,,,C0025349,D008599,,,,
+BMGC_DS01588,BMG_DS001998,,,,,,,DOID:1059,intellectual disability,C0025362,,,,,
+BMGC_DS01589,BMG_DS001999,,,,,,,DOID:2668,mesenchymoma,C0025464,,,MONDO:0006854,mesenchymoma,
+BMGC_DS01590,BMG_DS002000,,Mesenteric Lymphadenitis,Mesenteric Lymphadenitis,,,,DOID:10782,mesenteric lymphadenitis,C0025469,D008640,,MONDO:0001116,mesenteric lymphadenitis,
+BMGC_DS01591,BMG_DS002002,,Mesenteric Vascular Occlusion,Mesenteric Vascular Occlusion,,,,DOID:13252,mesenteric vascular occlusion,C0025472,D008641,,MONDO:0006855,mesenteric vascular occlusion,
+BMGC_DS01592,BMG_DS002003,,,,,,,DOID:4468,clear cell adenocarcinoma,C0025490,,,MONDO:0005613,mesonephric adenocarcinoma,
+BMGC_DS01593,BMG_DS002004,,,,,,,DOID:2645,benign mesothelioma,C0025500,,,MONDO:0005065,mesothelioma,
+BMGC_DS01594,BMG_DS002005,,Metabolic Diseases,Metabolic Diseases,,,,DOID:0014667,disease of metabolism,C0025517,D008659,,MONDO:0005066,metabolic disease,
+BMGC_DS01595,BMG_DS002006,,Inborn Errors of Metabolism,"Metabolism, Inborn Errors",,,,DOID:655,inherited metabolic disorder,C0025521,D008661,,MONDO:0019052,inborn errors of metabolism,
+BMGC_DS01596,BMG_DS002007,37832003,Metagonimiasis,Trematode Infections,1F8Z,"Diseases due to trematodes, unspecified",B66.8,DOID:884,metagonimiasis,C0025530,D014201,,MONDO:0004666,metagonimiasis,Infection by Metagonimus yokogawai | Metagonimiasis | Metagonimosis | Infection caused by Metagonimus yokogawai | Infection caused by Metagonimus yokogawai (disorder)
+BMGC_DS01597,BMG_DS002008,,"Metal Metabolism, Inborn Errors","Metal Metabolism, Inborn Errors",,,,DOID:896,metal metabolism disorder,C0025534,D008664,,MONDO:0004689,inborn metal metabolism disorder,
+BMGC_DS01598,BMG_DS002009,267549008;191386007;38959009,Methemoglobinemia,Methemoglobinemia,,,D74,DOID:10783,methemoglobinemia,C0025637,D008708,MTHU039706,MONDO:0001117,methemoglobinemia,Methaemoglobinaemia | Methemoglobinemia | Methaemoglobinaemia (disorder) | (Methemoglobinemia) or (Stokvis' disease) or (sulfemoglobinemia) | Stokvis' disease | Methemoglobinemia | Sulfemoglobinemia | Sulphaemoglobinaemia | Methaemoglobinaemia | (Methaemoglobinaemia) or (Stokvis' disease) or (sulphaemoglobinaemia) | (Methaemoglobinaemia) or (Stokvis' disease) or (sulphaemoglobinaemia) (disorder) | Methemoglobinemia | Methaemoglobinaemia | Methemoglobinemia (disorder)
+BMGC_DS01599,BMG_DS002010,,"Microangiopathy, Diabetic",Diabetic Angiopathies,,,,,,C0025945,D003925,,,,
+BMGC_DS01600,BMG_DS002011,,,,,,,DOID:10907,microcephaly,C0025958,,,MONDO:0016056,isolated congenital microcephaly,
+BMGC_DS01601,BMG_DS002012,,,,,,,DOID:10629,microphthalmia,C0026010,,,MONDO:0021129,microphthalmia,
+BMGC_DS01602,BMG_DS002013,,Middle Lobe Syndrome,Middle Lobe Syndrome,,,,DOID:2810,middle lobe syndrome,C0026069,D008878,,MONDO:0005847,middle lobe syndrome,
+BMGC_DS01603,BMG_DS002014,,Mikulicz Disease,Mikulicz' Disease,,,,DOID:12900,Mikulicz disease,C0026103,D008882,,MONDO:0019191,IgG4-related dacryoadenitis and sialadenitis,
+BMGC_DS01604,BMG_DS002015,63951004,Miliaria,Miliaria,,,,DOID:1382,miliaria,C0026113,D008883,,MONDO:0006580,miliaria,Miliaria | Miliaria (disorder)
+BMGC_DS01605,BMG_DS002017,,Milk-Alkali Syndrome,Hypercalcemia,,,,,,C0026141,D006934,,MONDO:0400002,calcium-alkali syndrome,
+BMGC_DS01606,BMG_DS002018,,Milker's Nodes,Poxviridae Infections,,,,DOID:8729,milker's nodule,C0026143,D011213,,MONDO:0005850,milker's nodule,
+BMGC_DS01607,BMG_DS002019,,Mite Infestations,Mite Infestations,,,,DOID:7894,mite infestation,C0026229,D008924,,MONDO:0004389,mite infestation,
+BMGC_DS01608,BMG_DS002020,,,,,,,DOID:61,mitral valve disease,C0026265,,,MONDO:0003767,mitral valve disorder,
+BMGC_DS01609,BMG_DS002021,,Mitral Valve Insufficiency,Mitral Valve Insufficiency,,,,DOID:11502,mitral valve insufficiency,C0026266,D008944,,MONDO:1030008,mitral valve insufficiency,
+BMGC_DS01610,BMG_DS002022,,Mitral Valve Prolapse Syndrome,Mitral Valve Prolapse,,,,DOID:988,mitral valve prolapse,C0026267,D008945,,MONDO:0004910,mitral valve prolapse,
+BMGC_DS01611,BMG_DS002023,,Mitral Valve Stenosis,Mitral Valve Stenosis,,,,DOID:1754,mitral valve stenosis,C0026269,D008946,,MONDO:0005852,mitral valve stenosis,
+BMGC_DS01612,BMG_DS002024,,Mixed Connective Tissue Disease,Mixed Connective Tissue Disease,,,,DOID:3492,mixed connective tissue disease,C0026272,D008947,,MONDO:0005854,mixed connective tissue disease,
+BMGC_DS01613,BMG_DS002025,,,,,,,DOID:452,pleomorphic adenoma,C0026277,,,,,
+BMGC_DS01614,BMG_DS002026,,Mohr Syndrome,Orofaciodigital Syndromes,,,,DOID:0060316,orofaciodigital syndrome I,C0026363,D009958,252100,MONDO:0009642,orofaciodigital syndrome type II,
+BMGC_DS01615,BMG_DS002027,,Molluscum Contagiosum,Molluscum Contagiosum,,,,DOID:8867,molluscum contagiosum,C0026393,D008976,,MONDO:0005855,molluscum contagiosum,
+BMGC_DS01616,BMG_DS002028,,Monieziasis,Monieziasis,,,,DOID:931,monieziasis,C0026414,D008989,,MONDO:0004755,monieziasis,
+BMGC_DS01617,BMG_DS002030,,,,,,,,,C0026470,,,MONDO:0004225,monoclonal gammopathy of uncertain significance,
+BMGC_DS01618,BMG_DS002031,,,,,,,DOID:2346,monoclonal paraproteinemia,C0026471,,,MONDO:0002274,monoclonal paraproteinemia disease,
+BMGC_DS01619,BMG_DS002033,,,,,,,DOID:2560,morphine dependence,C0026552,,,MONDO:0005531,morphine dependence,
+BMGC_DS01620,BMG_DS002034,,Motion Sickness,Motion Sickness,,,,DOID:2951,motion sickness,C0026603,D009041,158280,MONDO:0008015,motion sickness,
+BMGC_DS01621,BMG_DS002035,,,,,,,DOID:13711,dental fluorosis,C0026618,,,MONDO:0006722,dental fluorosis,
+BMGC_DS01622,BMG_DS002036,,Mouth Diseases,Mouth Diseases,,,,DOID:403,mouth disease,C0026636,D009059,,MONDO:0006858,mouth disorder,
+BMGC_DS01623,BMG_DS002037,,,,,,,,,C0026640,,,MONDO:0021245,oral cavity neoplasm,
+BMGC_DS01624,BMG_DS002038,,Movement Disorders,Movement Disorders,,,,DOID:480,movement disease,C0026650,D009069,,MONDO:0005395,movement disorder,
+BMGC_DS01625,BMG_DS002039,,Moyamoya Disease,Moyamoya Disease,,,,DOID:13099,Moyamoya disease,C0026654,D009072,,MONDO:0016820,Moyamoya disease,
+BMGC_DS01626,BMG_DS002040,53773002,Mucocele of appendix,,,,,DOID:13248,mucocele of appendix,C0026684,,,MONDO:0001671,mucocele of appendix,Mucocele of appendix | Mucocele of appendix (disorder) | Appendicular mucocele | Mucocoele of appendix
+BMGC_DS01627,BMG_DS002041,,,,,,,DOID:12904,mucocele of salivary gland,C0026686,,,MONDO:0001600,mucocele of salivary gland,
+BMGC_DS01628,BMG_DS002042,,Mucocutaneous Lymph Node Syndrome,Mucocutaneous Lymph Node Syndrome,,,,DOID:13378,Kawasaki disease,C0026691,D009080,611775,MONDO:0012727,mucocutaneous lymph node syndrome,
+BMGC_DS01629,BMG_DS002043,,Mucolipidoses,Mucolipidoses,,,,DOID:3343,glycoproteinosis,C0026697,D009081,,MONDO:0019248,mucolipidosis,
+BMGC_DS01630,BMG_DS002044,,Mucopolysaccharidoses,Mucopolysaccharidoses,,,,DOID:12798,mucopolysaccharidosis,C0026703,D009083,,MONDO:0019249,mucopolysaccharidosis,
+BMGC_DS01631,BMG_DS002045,,Mucopolysaccharidosis II,Mucopolysaccharidosis II,,,,DOID:12799,mucopolysaccharidosis II,C0026705,D016532,309900,MONDO:0010674,mucopolysaccharidosis type 2,
+BMGC_DS01632,BMG_DS002046,,Mucopolysaccharidosis III,Mucopolysaccharidosis III,,,,DOID:12801,mucopolysaccharidosis III,C0026706,D009084,,MONDO:0018937,mucopolysaccharidosis type 3,
+BMGC_DS01633,BMG_DS002047,,Mucopolysaccharidosis IV,Mucopolysaccharidosis IV,,,,DOID:12804,mucopolysaccharidosis IV,C0026707,D009085,,MONDO:0018938,mucopolysaccharidosis type 4,
+BMGC_DS01634,BMG_DS002048,,Mucopolysaccharidosis V,Mucopolysaccharidosis I,,,,,,C0026708,D008059,607016,MONDO:0011760,Scheie syndrome,
+BMGC_DS01635,BMG_DS002049,,Mucopolysaccharidosis VI,Mucopolysaccharidosis VI,,,,DOID:12800,mucopolysaccharidosis VI,C0026709,D009087,253200,MONDO:0009661,mucopolysaccharidosis type 6,
+BMGC_DS01636,BMG_DS002050,76627001;187098003,Mucormycosis,Mucormycosis,,,,DOID:8485,mucormycosis,C0026718,D009091,,,,Mucormycosis | Mucormycosis (disorder) | Zygomycosis (& [mucormycosis]) | Zygomycosis | Phycomycosis | Mucormycosis | Zygomycosis (& [mucormycosis]) (disorder)
+BMGC_DS01637,BMG_DS002051,,Multiple Carboxylase Deficiency,Multiple Carboxylase Deficiency,,,,DOID:857,multiple carboxylase deficiency,C0026755,D009100,,MONDO:0015454,multiple carboxylase deficiency,
+BMGC_DS01638,BMG_DS002052,,,,,,,DOID:12721,multiple epiphyseal dysplasia,C0026760,,,MONDO:0016648,multiple epiphyseal dysplasia,
+BMGC_DS01639,BMG_DS002053,,,,,,,DOID:9538,multiple myeloma,C0026764,,254500,MONDO:0009693,plasma cell myeloma,
+BMGC_DS01640,BMG_DS002054,,Multiple Organ Failure,Multiple Organ Failure,,,,,,C0026766,D009102,,MONDO:0043726,multiple organ dysfunction syndrome,
+BMGC_DS01641,BMG_DS002055,,Multiple Sclerosis,Multiple Sclerosis,,,,DOID:2377,multiple sclerosis,C0026769,D009103,,MONDO:0005301,multiple sclerosis,
+BMGC_DS01642,BMG_DS002056,,,,,,,DOID:10934,multiple personality disorder,C0026773,,,MONDO:0001159,multiple personality disorder,
+BMGC_DS01643,BMG_DS002057,154352008;36989005,Mumps,Mumps,,,B26,DOID:10264,mumps,C0026780,D009107,,MONDO:0000989,mumps infectious disease,Mumps | Mumps (disorder)
+BMGC_DS01644,BMG_DS002058,,,,,,,DOID:767,muscular atrophy,C0026846,,,,,
+BMGC_DS01645,BMG_DS002059,,Spinal Muscular Atrophy,"Muscular Atrophy, Spinal",,,,DOID:12377,spinal muscular atrophy,C0026847,D009134,,MONDO:0001516,spinal muscular atrophy,
+BMGC_DS01646,BMG_DS002060,155094005;52794005;267711006;129565002,Myopathy,Muscular Diseases,,,,DOID:423,myopathy,C0026848,D009135,MTHU003653,MONDO:0005336;MONDO:0003939,myopathy | muscle tissue disorder,Muscular dystrophy/myopathies | Myopathy | Muscular dystrophy &/or myopathies | Muscular dystrophy &/or myopathies (disorder) | Myopathy | Myopathic syndrome | Myopathic disease | Myopathy (disorder) | Myopathy | Muscular dystrophy/myopathies | Muscular dystrophy &/or myopathies | Muscular dystrophy &/or myopathies (disorder) | Disorder of muscle | Disorder of skeletal AND/OR smooth muscle (disorder) | Myopathic disease | Myopathy | Disorder of skeletal AND/OR smooth muscle
+BMGC_DS01647,BMG_DS002062,,Muscular Dystrophy,Muscular Dystrophies,,,,DOID:9884,muscular dystrophy,C0026850,D009136,,MONDO:0020121,muscular dystrophy,
+BMGC_DS01648,BMG_DS002063,,"Muscular Dystrophy, Animal","Muscular Dystrophy, Animal",,,,,,C0026851,D009137,,MONDO:0024965,"muscular dystrophy, non-human animal",
+BMGC_DS01649,BMG_DS002064,,Musculoskeletal Diseases,Musculoskeletal Diseases,,,,DOID:17,musculoskeletal system disease,C0026857,D009140,,MONDO:0002081,musculoskeletal system disorder,
+BMGC_DS01650,BMG_DS002065,88052002;267771000,Mutism,Mutism,,,,DOID:4189,mutism,C0026884,D009155,MTHU001337,MONDO:0002905,mutism,Mutism | Muteness | Mutism (finding) | Mutism | Deaf mutism NOS | (Mutism) or (deaf mutism NOS) | (Mutism) or (deaf mutism NOS) (disorder)
+BMGC_DS01651,BMG_DS002066,,Myasthenia Gravis,Myasthenia Gravis,,,,DOID:437,myasthenia gravis,C0026896,D009157,254200,MONDO:0009688,myasthenia gravis,
+BMGC_DS01652,BMG_DS002068,,Mycobacterium avium-intracellulare Infection,Mycobacterium avium-intracellulare Infection,,,,DOID:2755,Mycobacterium avium complex disease,C0026916,D015270,,MONDO:0005866,Mycobacterium avium complex disease,
+BMGC_DS01653,BMG_DS002069,,Mycobacterium Infections,Mycobacterium Infections,,,,,,C0026918,D009164,,MONDO:0020590,mycobacterial infectious disease,
+BMGC_DS01654,BMG_DS002070,,"Mycobacterium Infections, Nontuberculous","Mycobacterium Infections, Nontuberculous",,,,,,C0026919,D009165,,,,
+BMGC_DS01655,BMG_DS002071,,Mycoplasma Infections,Mycoplasma Infections,,,,,,C0026936,D009175,,,,
+BMGC_DS01656,BMG_DS002073,154394006;187472001;154393000;266214005;3218000,Mycoses,Mycoses,,,,DOID:1564,fungal infectious disease,C0026946,D009181,,MONDO:0002041,fungal infectious disease,(Dermatophytosis &/or tinea &/or ringworm) or (fungal infections) or (mycoses) | Fungal infection | Dermatophytosis | Tinea | Fungal infections | Mycoses | Ringworm | Dermatophytosis-tinea/ringworm | (Dermatophytosis &/or tinea &/or ringworm) or (fungal infections) or (mycoses) (disorder) | Mycoses | Mycoses (disorder) | Ringworm | Mycoses | Dermatophytosis-tinea/ringworm | Tinea | Fungal infection | Dermatophytosis | Fungal infections | (Dermatophytosis &/or tinea &/or ringworm) or (fungal infections) or (mycoses) | (Dermatophytosis &/or tinea &/or ringworm) or (fungal infections) or (mycoses) (disorder) | Mycosis | Fungal infection | Disease caused by fungus | Fungal infectious disease | Fungus infection | Mycoses | Mycosis (disorder) | Mycotic disease
+BMGC_DS01657,BMG_DS002074,,,,,,,DOID:8691,mycosis fungoides,C0026948,,254400,MONDO:0009691,mycosis fungoides,
+BMGC_DS01658,BMG_DS002075,267682000;41370002;192682002,Myelitis,Myelitis,,,,DOID:322,myelitis,C0026975,D009187,,MONDO:0002565,myelitis,"Myelitis | Encephalitis | Encephalitis/myelitis | Encephalitis &/or myelitis | Encephalitis &/or myelitis (disorder) | Myelitis | Myelitis (disorder) | Encephalitis &/or myelitis &/or encephalomyelitis &/or transverse myelitis | Encephalitis, myelitis and encephalomyelitis | Transverse myelitis | Myelitis | Encephalomyelitis | Encephalitis &/or myelitis &/or encephalomyelitis &/or transverse myelitis (disorder)"
+BMGC_DS01659,BMG_DS002076,,"Myelitis, Transverse","Myelitis, Transverse",,,,,,C0026976,D009188,,MONDO:0021553,transverse myelitis,
+BMGC_DS01660,BMG_DS002077,,,,,,,DOID:4971,myelofibrosis,C0026987,,,MONDO:0044903,myelofibrosis,
+BMGC_DS01661,BMG_DS002078,,,,,,,DOID:0081086,acute myeloid leukemia without maturation,C0026998,,,MONDO:0005224,acute myeloblastic leukemia without maturation,
+BMGC_DS01662,BMG_DS002079,,,,,,,DOID:4960,bone marrow cancer,C0027022,,,,,
+BMGC_DS01663,BMG_DS002080,266225001;154423006;60412004,Myiasis,Myiasis,,,B87,DOID:11080,myiasis,C0027030,D009198,,MONDO:0019147,myiasis,(Other infectious & parasitic disease) or (infestation: [leech] or [maggot]) or (myiasis) or (toxoplasmosis) | Myiasis | Toxoplasmosis | Other infectious and parasitic diseases | Maggot infestation | Leech infestation | Other infect. and parasit.dis. | (Other infectious & parasitic disease) or (infestation: [leech] or [maggot]) or (myiasis) or (toxoplasmosis) (disorder) | Maggot infestation | Myiasis | Toxoplasmosis | Leech infestation | Other infectious and parasitic diseases | Other infect. and parasit.dis. | (Other infectious & parasitic disease) or (infestation: [leech] or [maggot]) or (myiasis) or (toxoplasmosis) | (Other infectious & parasitic disease) or (infestation: [leech] or [maggot]) or (myiasis) or (toxoplasmosis) (disorder) | Infestation by fly larvae | Infestation by maggots | Myiasis | Myiasis - fly larvae infestation | Fly larva infestation | Infestation caused by fly larvae (disorder) | Infestation caused by maggots | Infestation caused by fly larvae
+BMGC_DS01664,BMG_DS002086,,,,,,,DOID:5039,myoblastoma,C0027043,,,MONDO:0003250,benign granular cell tumor,
+BMGC_DS01665,BMG_DS002087,,Myocardial Infarction,Myocardial Infarction,,,,DOID:5844,myocardial infarction,C0027051,D009203,,MONDO:0005068,myocardial infarction,
+BMGC_DS01666,BMG_DS002088,50920009,Myocarditis,Myocarditis,,,,DOID:820,myocarditis,C0027059,D009205,MTHU056479,MONDO:0004496,myocarditis,Myocarditis | Myocarditis (disorder) | Myocardial inflammation
+BMGC_DS01667,BMG_DS002089,37925008,Interstitial myocarditis,,,,,DOID:817,interstitial myocarditis,C0027060,,,MONDO:0004485,interstitial myocarditis,Interstitial myocarditis | Interstitial myocarditis (disorder)
+BMGC_DS01668,BMG_DS002091,,,,,,,DOID:2661,myoepithelioma,C0027070,,,MONDO:0002380,myoepithelial tumor,
+BMGC_DS01669,BMG_DS002092,,Myofascial Pain Syndromes,Myofascial Pain Syndromes,,,,DOID:431,myofascial pain syndrome,C0027073,D009209,,MONDO:0006862,myofascial pain syndrome,
+BMGC_DS01670,BMG_DS002093,,,,,,,DOID:2691,myoma,C0027086,,,MONDO:0003061,benign muscle neoplasm,
+BMGC_DS01671,BMG_DS002094,155133003;57190000,Myopia,Myopia,9D00.0,Myopia,H52.1,DOID:11830,myopia,C0027092,D009216,MTHU036427,MONDO:0001384,myopia,Myopia | Myopia (disorder) | Myopia | Nearsightedness | Myopia (disorder) | Near sighted
+BMGC_DS01672,BMG_DS002095,,,,,,,DOID:4045,muscle cancer,C0027095,,,,,
+BMGC_DS01673,BMG_DS002096,26889001,Myositis,Myositis,,,M60,DOID:633,myositis,C0027121,D009220,MTHU062042,MONDO:0021167,myositis disease,Myositis | Myositis (disorder) | Muscle inflammation | Inflammatory disorder of muscle | Inflammatory myopathy
+BMGC_DS01674,BMG_DS002097,,Myositis Ossificans,Myositis Ossificans,,,,DOID:668,myositis ossificans,C0027122,D009221,,MONDO:0003964,myositis ossificans,
+BMGC_DS01675,BMG_DS002099,,Myotonic Dystrophy,Myotonic Dystrophy,,,,DOID:11722,myotonic dystrophy type 1,C0027126,D009223,,MONDO:0016107,myotonic dystrophy,
+BMGC_DS01676,BMG_DS002100,,Myotonia Congenita,Myotonia Congenita,,,,DOID:2106,myotonia congenita,C0027127,D009224,255300,MONDO:0100468;MONDO:0009710,Batten-Turner congenital myopathy | Thomsen and Becker disease,
+BMGC_DS01677,BMG_DS002101,64741003,Myotonic cataract,,,,,DOID:82,myotonic cataract,C0027128,,,MONDO:0004495,myotonic cataract,Myotonic cataract | Myotonic cataract (disorder)
+BMGC_DS01678,BMG_DS002103,190274003;43153006;154660000;267465007,Myxedema,Myxedema,,,,DOID:11634,myxedema,C0027145,D009230,255900,MONDO:0009718,myxedema,Hypothyroidism | Acquired hypothyroidism | Thyroid deficiency | Hypothyroidism: &/or (acquired) | Myxedema | Myxoedema | Hypothyroidism: &/or (acquired) (disorder) | Myxedema | Myxoedema | Myxedema (disorder) | Cretinism | Hypothyroidism | Hypothyroidism - congenital and acquired | Hypothyroidism-congen.+ acqui. | Hypothyroidism - congenital and acquired (& [cretinism] or [myxedema]) | Hypothyroidism - congenital and acquired (& [cretinism] or [myxoedema]) | Myxedema | Myxoedema | Hypothyroidism - congenital and acquired (& [cretinism] or [myxoedema]) (disorder) | Hypothyroidism - congenital and acquired (& [cretinism] or [myxedema]) | Cretinism | Hypothyroidism-congen.+ acqui. | Hypothyroidism - congenital and acquired | Hypothyroidism | Myxoedema | Hypothyroidism - congenital and acquired (& [cretinism] or [myxoedema]) | Myxedema | Hypothyroidism - congenital and acquired (& [cretinism] or [myxoedema]) (disorder)
+BMGC_DS01679,BMG_DS002106,,,,,,,DOID:4136,myxosarcoma,C0027155,,,MONDO:0006863,myxosarcoma,
+BMGC_DS01680,BMG_DS002109,,Nail Diseases,Nail Diseases,,,,DOID:4123,nail disease,C0027339,D009260,,MONDO:0002884,nail disorder,
+BMGC_DS01681,BMG_DS002110,,Nail-Patella Syndrome,Nail-Patella Syndrome,,,,DOID:9467,nail-patella syndrome,C0027341,D009261,161200,MONDO:0008061,nail-patella syndrome,
+BMGC_DS01682,BMG_DS002112,,,,,,,DOID:2745,narcissistic personality disorder,C0027402,,,MONDO:0002411,narcissistic personality disorder,
+BMGC_DS01683,BMG_DS002113,155059003;267702006;60380001,Narcolepsy,Narcolepsy,,,G47.41,DOID:8986,narcolepsy,C0027404,D009290,MTHU039740,MONDO:0021107,narcolepsy,(CNS disorders NOS) or (narcolepsy) or (Ondine's curse) or (Schilder's disease) | CNS disorders NOS | Narcolepsy | Schilder's disease | Ondine's curse | (CNS disorders NOS) or (narcolepsy) or (Ondine's curse) or (Schilder's disease) (disorder) | Narcolepsy | Ondine's curse | Schilder's disease | CNS disorders NOS | (CNS disorders NOS) or (narcolepsy) or (Ondine's curse) or (Schilder's disease) | (CNS disorders NOS) or (narcolepsy) or (Ondine's curse) or (Schilder's disease) (disorder) | Narcolepsy | Paroxysmal sleep | Gelineau's syndrome | Narcolepsy (disorder) | Narcoleptic syndrome
+BMGC_DS01684,BMG_DS002114,,,,,,,,,C0027430,,,MONDO:0006314,nasal cavity polyp,
+BMGC_DS01685,BMG_DS002116,,Nasopharyngeal Diseases,Nasopharyngeal Diseases,,,,DOID:9561,nasopharyngeal disease,C0027438,D009302,,MONDO:0004821,nasopharyngeal disorder,
+BMGC_DS01686,BMG_DS002117,,,,,,,,,C0027439,,,MONDO:0005375,nasopharyngeal neoplasm,
+BMGC_DS01687,BMG_DS002118,51476001,Nasopharyngitis,Nasopharyngitis,,,,DOID:10460,nasopharyngitis,C0027441,D009304,,MONDO:0001040,nasopharyngitis,Nasopharyngitis | Rhinopharyngitis | Nasopharyngitis (disorder)
+BMGC_DS01688,BMG_DS002119,,,,,,,,,C0027443,,187050,MONDO:0008532,teeth present at birth,
+BMGC_DS01689,BMG_DS002120,36667009,Necatoriasis,Necatoriasis,1F68.1,Necatoriasis,B76.1,DOID:2790,necatoriasis,C0027528,D009332,,MONDO:0005870,necatoriasis,Necatoriasis | Necatorosis | Necatoriasis (disorder)
+BMGC_DS01690,BMG_DS002124,,Necrobiosis Lipoidica,Necrobiosis Lipoidica,,,,DOID:3486,necrobiosis lipoidica,C0027538,D009335,,MONDO:0006583,necrobiosis lipoidica,
+BMGC_DS01691,BMG_DS002125,397758007;34686004;156837008,Avascular necrosis of bone,,,,,DOID:10159,osteonecrosis,C0027543,,,MONDO:0018373,avascular necrosis,Avascular necrosis of bone (disorder) | Avascular necrosis of bone | AVN (avascular necrosis) of bone | Osteonecrosis | Bone necrosis | Aseptic necrosis of bone | Aseptic necrosis of bone | AVN - Avascular necrosis of bone | Osteonecrosis | Aseptic necrosis | Avascular necrosis of bone | Aseptic necrosis of bone (disorder) | Avascular necrosis of bone | Avascular necrosis of bone (disorder)
+BMGC_DS01692,BMG_DS002127,,,,,,,DOID:4968,Nelson syndrome,C0027577,,,,,
+BMGC_DS01693,BMG_DS002129,,"Infections, Nematomorpha",Helminthiasis,,,,,,C0027585,D006373,,,,
+BMGC_DS01694,BMG_DS002130,414819007,Neonatal Abstinence Syndrome,Neonatal Abstinence Syndrome,,,,DOID:9828,neonatal abstinence syndrome,C0027609,D009357,,MONDO:0005566,neonatal abstinence syndrome,Neonatal withdrawal syndrome | Neonatal abstinence syndrome | Neonatal abstinence syndrome (disorder) | Neonatal withdrawal symptoms from maternal use of drugs of addiction | Substance withdrawal syndrome in neonate of dependent mother | Substance withdrawal syndrome in newborn | Neonatal substance withdrawal syndrome
+BMGC_DS01695,BMG_DS002131,206345004,Neonatal dacryocystitis and conjunctivitis (disorder),,,,,DOID:9699,ophthalmia neonatorum,C0027611,,,,,Neonatal dacryocystitis and conjunctivitis | Neonatal dacryocystitis and conjunctivitis (disorder)
+BMGC_DS01696,BMG_DS002132,,"Congenital, Hereditary, and Neonatal Diseases and Abnormalities","Congenital, Hereditary, and Neonatal Diseases and Abnormalities",,,,,,C0027612,D009358,,,,
+BMGC_DS01697,BMG_DS002134,,,,,,,,,C0027651,,,MONDO:0005070,neoplasm,
+BMGC_DS01698,BMG_DS002135,,,,,,,DOID:688,embryonal cancer,C0027654,,,MONDO:0005564,embryonal neoplasm,
+BMGC_DS01699,BMG_DS002136,,,,,,,DOID:201,connective tissue cancer,C0027656,,,MONDO:0021581,connective tissue neoplasm,
+BMGC_DS01700,BMG_DS002137,,,,,,,DOID:3095,germ cell and embryonal cancer,C0027658,,,,,
+BMGC_DS01701,BMG_DS002138,,,,,,,,,C0027662,,,MONDO:0017169,multiple endocrine neoplasia,
+BMGC_DS01702,BMG_DS002139,,,,,,,DOID:461,muscle benign neoplasm,C0027664,,,,,
+BMGC_DS01703,BMG_DS002140,,,,,,,DOID:3093,nervous system cancer,C0027665,,,,,
+BMGC_DS01704,BMG_DS002142,,,,,,,,,C0027672,,,MONDO:0015356,hereditary neoplastic syndrome,
+BMGC_DS01705,BMG_DS002143,52845002,Nephritis,Nephritis,,,N08,DOID:10952,nephritis,C0027697,D009393,MTHU036910,MONDO:0001166,nephritis,Nephritis | Nephritis (disorder)
+BMGC_DS01706,BMG_DS002144,57333009;399340005,Hereditary nephritis,,,,,DOID:10983,Alport syndrome,C0027706,,,MONDO:0005334,hereditary nephritis,Hereditary nephritis | Alport's syndrome | Familial nephritis | Familial hematuria | Hereditary glomerulonephritis | GN - Hereditary glomerulonephritis | Non-progressive hereditary glomerulonephritis | Benign familial haematuria | Benign familial hematuria | Familial haematuria | Hereditary nephritis (disorder) | Hereditary nephritis (disorder) | Hereditary nephritis | GN - Hereditary glomerulonephritis | Hereditary glomerulonephritis
+BMGC_DS01707,BMG_DS002145,,"Nephritis, Interstitial","Nephritis, Interstitial",,,,DOID:1063,interstitial nephritis,C0027707,D009395,,,,
+BMGC_DS01708,BMG_DS002146,,,,,,,DOID:2154,nephroblastoma,C0027708,,,MONDO:0006058,Wilms tumor,
+BMGC_DS01709,BMG_DS002147,190863003;267505006;48638002;154752005,Nephrocalcinosis,Nephrocalcinosis,,,,DOID:12679,nephrocalcinosis,C0027709,D009397,MTHU005829,MONDO:0001567,nephrocalcinosis,"(Disorders of calcium metabolism [& calcinosis]) or (nephrocalcinosis) | Calcinosis | Nephrocalcinosis | Disorders of calcium metabolism | (Disorders of calcium metabolism [& calcinosis]) or (nephrocalcinosis) (disorder) | (Phosphorus &/or calcium disorders (& [hypercalcemia] or [hypercalcinuria] or [hypocalcemia]) or (nephrocalcinosis) | Nephrocalcinosis | Calcium disorder | Phosphorus, calcium disorders | Hypercalcinuria | Phosphorus and calcium disorders | Phosphorus disorder | Hypocalcaemia | Hypercalcaemia | (Phosphorus &/or calcium disorders (& [hypercalcaemia] or [hypercalcinuria] or [hypocalcaemia]) or (nephrocalcinosis) | Hypercalcemia | Hypocalcemia | (Phosphorus &/or calcium disorders (& [hypercalcaemia] or [hypercalcinuria] or [hypocalcaemia]) or (nephrocalcinosis) (disorder) | Nephrocalcinosis | Nephrocalcinosis (disorder) | (Phosphorus &/or calcium disorders (& [hypercalcemia] or [hypercalcinuria] or [hypocalcemia]) or (nephrocalcinosis) | Nephrocalcinosis | Phosphorus and calcium disorders | Phosphorus, calcium disorders | Hypercalcinuria | Phosphorus disorder | Calcium disorder | (Phosphorus &/or calcium disorders (& [hypercalcaemia] or [hypercalcinuria] or [hypocalcaemia]) or (nephrocalcinosis) | Hypercalcemia | Hypocalcemia | Hypocalcaemia | Hypercalcaemia | (Phosphorus &/or calcium disorders (& [hypercalcaemia] or [hypercalcinuria] or [hypocalcaemia]) or (nephrocalcinosis) (disorder)"
+BMGC_DS01710,BMG_DS002148,194773000;32916005,Nephrosclerosis,Nephrosclerosis,,,,DOID:11664,nephrosclerosis,C0027719,D009400,MTHU036895,MONDO:0006044,nephrosclerosis,Hypertensive renal disease (& [nephrosclerosis]) | Hypertensive renal disease | Nephrosclerosis | Hypertensive nephropathy | Hypertensive renal disease (& [nephrosclerosis]) (disorder) | Nephrosclerosis | Interstitial arteriosclerotic nephritis | Chronic arteriosclerotic nephritis | Arteriosclerosis of kidney | Renal arteriosclerosis | Nephrosclerosis (disorder) | Renal sclerosis
+BMGC_DS01711,BMG_DS002149,90708001,Nephrosis,Nephrosis,,,,DOID:2527,nephrosis,C0027720,D009401,MTHU017719,MONDO:0002331,nephrosis,Kidney disease | Renal disorder | Nephropathy | Renal disease | Disease of kidney | Kidney disease (disorder) | Disorder of kidney
+BMGC_DS01712,BMG_DS002150,197592009;44785005,Lipoid nephrosis,,,,,DOID:10966,lipoid nephrosis,C0027721,,,MONDO:0006835,lipoid nephrosis,Nephrotic syndrome (& [minimal change glomerulonephritis] or [steroid sensitive]) | Nephrotic syndrome with minimal change glomerulonephritis | Steroid sensitive nephrotic syndrome | Lipoid nephrosis | Nephrotic syndrome (& [minimal change glomerulonephritis] or [steroid sensitive]) (disorder) | Minimal change disease | Nil disease | Lipoid nephrosis | Lipid nephrosis | Minimal change disease (disorder) | MCD - Minimal change disease | MCGN - Minimal change glomerulonephritis | Minimal change nephrotic syndrome | Minimal change nephropathy | Light negative glomerulonephritis | Minimal change glomerulonephritis | MCNS - Minimal change nephrotic syndrome | MCN - Minimal change nephropathy
+BMGC_DS01713,BMG_DS002151,,Nephrotic Syndrome,Nephrotic Syndrome,,,,DOID:1184,nephrotic syndrome,C0027726,D009404,,MONDO:0005377,nephrotic syndrome,
+BMGC_DS01714,BMG_DS002152,,,,,,,DOID:573,nerve compression syndrome,C0027743,,,,,
+BMGC_DS01715,BMG_DS002153,,,,,,,,,C0027746,,,MONDO:0005559,neurodegenerative disease,
+BMGC_DS01716,BMG_DS002154,,,,,,,DOID:863,nervous system disease,C0027765,,,MONDO:0005071,nervous system disorder,
+BMGC_DS01717,BMG_DS002156,42681006,Nesidioblastosis,Nesidioblastosis,,,,DOID:13317,hyperinsulinemic hypoglycemia,C0027773,D046768,,,,Islet cell hyperplasia | Nesidioblastosis | Pancreatic endocrine cell hyperplasia | Islet cell hyperplasia (disorder)
+BMGC_DS01718,BMG_DS002157,,,,,,,,,C0027794,,,MONDO:0018075,neural tube defect,
+BMGC_DS01719,BMG_DS002158,,,,,,,,,C0027796,,,MONDO:0021667,neuralgia,
+BMGC_DS01720,BMG_DS002160,,,,,,,DOID:3192,neurilemmoma,C0027809,,,MONDO:0002546,schwannoma,
+BMGC_DS01721,BMG_DS002161,247378004;123254001;84299009;21018002,Neuritis,Neuritis,,,,DOID:1803,neuritis,C0027813,D009443,,MONDO:0002122,neuritis,Neuritis | Neuritis (disorder) | Neuritis (disorder) | Neuritis | Inflammatory neuropathy | Inflammatory neuropathy (disorder) | Neuritis
+BMGC_DS01722,BMG_DS002162,,,,,,,DOID:769,neuroblastoma,C0027819,,,MONDO:0005072,neuroblastoma,
+BMGC_DS01723,BMG_DS002163,,Neurocirculatory Asthenia,,,,,DOID:11569,neurocirculatory asthenia,C0027821,D009449,,,,
+BMGC_DS01724,BMG_DS002164,156383005;267854005,Neurodermatitis,Neurodermatitis,,,,DOID:3309,neurodermatitis,C0027822,D009450,,MONDO:0006585,neurodermatitis,Neurodermatitis | Neurodermatitis (disorder)
+BMGC_DS01725,BMG_DS002165,,,,,,,DOID:962,neurofibroma,C0027830,,,MONDO:0016755,neurofibroma,
+BMGC_DS01726,BMG_DS002166,,,,,,,DOID:0111253,neurofibromatosis 1,C0027831,,162200,MONDO:0018975,neurofibromatosis type 1,
+BMGC_DS01727,BMG_DS002167,,,,,,,DOID:0111252,vestibular schwannomatosis,C0027832,,101000,MONDO:0007039,NF2-related schwannomatosis,
+BMGC_DS01728,BMG_DS002168,,Neuroleptic Malignant Syndrome,Neuroleptic Malignant Syndrome,,,,DOID:14464,neuroleptic malignant syndrome,C0027849,D009459,,MONDO:0019790,neuroleptic malignant syndrome,
+BMGC_DS01729,BMG_DS002169,,,,,,,DOID:2001,neuroma,C0027858,,,MONDO:0002173,neuroma,
+BMGC_DS01730,BMG_DS002170,,,,,,,DOID:12689,acoustic neuroma,C0027859,,,MONDO:0001569,acoustic neuroma,
+BMGC_DS01731,BMG_DS002171,,Neuromuscular Diseases,Neuromuscular Diseases,,,,DOID:440,neuromuscular disease,C0027868,D009468,,MONDO:0019056,neuromuscular disease,
+BMGC_DS01732,BMG_DS002172,,Neuromyelitis Optica,Neuromyelitis Optica,,,,DOID:8869,neuromyelitis optica,C0027873,D009471,,MONDO:0019100,neuromyelitis optica,
+BMGC_DS01733,BMG_DS002173,,Neuronal Ceroid-Lipofuscinoses,Neuronal Ceroid-Lipofuscinoses,,,,DOID:14503,neuronal ceroid lipofuscinosis,C0027877,D009472,,MONDO:0016295,neuronal ceroid lipofuscinosis,
+BMGC_DS01734,BMG_DS002174,,,,,,,DOID:8117,neuronitis,C0027881,,,MONDO:0004466,neuronitis,
+BMGC_DS01735,BMG_DS002175,,Hereditary Motor and Sensory Neuropathies,Hereditary Sensory and Motor Neuropathy,,,,DOID:2477,motor peripheral neuropathy,C0027888,D015417,,MONDO:0015358,hereditary motor and sensory neuropathy,
+BMGC_DS01736,BMG_DS002176,,Hereditary Sensory and Autonomic Neuropathies,Hereditary Sensory and Autonomic Neuropathies,,,,DOID:0050548,hereditary sensory neuropathy,C0027889,D009477,,MONDO:0015364,hereditary sensory and autonomic neuropathy,
+BMGC_DS01737,BMG_DS002177,26039008;266210001;154384001;186884004,Neurosyphilis,Neurosyphilis,,,,DOID:9988,tertiary neurosyphilis,C0027927,D009494,,MONDO:0004944,neurosyphilis,Neurosyphilis | Syphilis of central nervous system | Neurosyphilis (disorder) | Neurosyphilis (& [GPI] or [tabes dorsalis]) | GPI-general paralysis insane | GPI - General paresis of the insane | Tabes dorsalis | Neurosyphilis | Neurosyphilis (& [GPI] or [tabes dorsalis]) (disorder) | Neurosyphilis (& [GPI] or [tabes dorsalis]) | GPI - General paresis of the insane | Neurosyphilis | GPI-general paralysis insane | Tabes dorsalis | Neurosyphilis (& [GPI] or [tabes dorsalis]) (disorder) | Neurosyphilis | Neurosyphilis (disorder)
+BMGC_DS01738,BMG_DS002178,,,,,,,DOID:4964,neurotic disorder,C0027932,,,MONDO:0005379,neurotic disorder,
+BMGC_DS01739,BMG_DS002179,191336001;72885007;303011007;142928004,Neutropenia,Neutropenia,,,D70,DOID:1227;DOID:0050590,neutropenia | severe congenital neutropenia,C0027947,D009503,MTHU001686,,,(Agranulocytosis) or (Kostmann's syndrome) or (neutropenia) | Kostmann's syndrome | Neutropenia | Agranulocytosis | (Agranulocytosis) or (Kostmann's syndrome) or (neutropenia) (disorder) | Neutropenia | Neutropenia (disorder) | Neutropenic disorder | Neutropenic disorder (disorder) | Neutropenia | Neutropenia (finding)
+BMGC_DS01740,BMG_DS002181,,,,,,,,,C0027962,,,MONDO:0005073,melanocytic nevus,
+BMGC_DS01741,BMG_DS002182,,Newcastle Disease,Newcastle Disease,,,,DOID:2929,Newcastle disease,C0027983,D009521,,MONDO:0005875,Newcastle disease,
+BMGC_DS01742,BMG_DS002183,,,,,,,DOID:0050742,nicotine dependence,C0028043,,,MONDO:0008575,nicotine dependence,
+BMGC_DS01743,BMG_DS002184,,Niemann-Pick Diseases,Niemann-Pick Diseases,,,,DOID:14504,Niemann-Pick disease,C0028064,D009542,,MONDO:0001982,Niemann-Pick disease,
+BMGC_DS01744,BMG_DS002185,65194006;75390007,Nyctalopia,Night Blindness,,,,DOID:8499,night blindness,C0028077,D009755,MTHU008883,MONDO:0004588,night blindness,Night blindness | Nyctalopia | Night blindness (disorder) | Difficulty seeing at night | Day blindness | Hemeralopia | Difficulty seeing at night | Night blindness | Nyctalopia | Day blindness (disorder)
+BMGC_DS01745,BMG_DS002186,,Nocardia Infections,Nocardia Infections,,,,DOID:2312,nocardiosis,C0028242,D009617,,MONDO:0017776,nocardiosis,
+BMGC_DS01746,BMG_DS002188,,,,,,,DOID:14116,multiple symmetric lipomatosis,C0028253,,,,,
+BMGC_DS01747,BMG_DS002190,18116006;196528007,Noma,Noma,1C1H.Z,"Necrotising ulcerative gingivitis, unspecified",A69.0,DOID:9672,noma,C0028271,D009625,,MONDO:0017124,noma,Cancrum oris | Gangrenous stomatitis | Noma | Acute gangrenous stomatitis | Cancrum oris (disorder) | Noma (& [cancrum oris] or [gangrenous stomatitis]) | Cancrum oris | Noma | Gangrenous stomatitis | Noma (& [cancrum oris] or [gangrenous stomatitis]) (disorder)
+BMGC_DS01748,BMG_DS002193,,Noonan Syndrome,Noonan Syndrome,,,,DOID:3490,Noonan syndrome,C0028326,D009634,,MONDO:0018997,Noonan syndrome,
+BMGC_DS01749,BMG_DS002194,128870005,Crusted scabies,,,,,DOID:14374,norwegian scabies,C0028425,,,MONDO:0001951,Norwegian scabies,Norwegian scabies | Crusted scabies | Crusted scabies (disorder)
+BMGC_DS01750,BMG_DS002195,,Nose Diseases,Nose Diseases,,,,DOID:2825,nose disease,C0028432,D009668,,MONDO:0002436,nasal disorder,
+BMGC_DS01751,BMG_DS002198,6408001;139394000,Nocturia,Nocturia,,,R35.1,,,C0028734,D053158,MTHU037390,,,Nycturia | Nocturia - finding | Finding of nocturia (finding) | Finding of nocturia | Nocturia | Nocturia (finding)
+BMGC_DS01752,BMG_DS002199,194171007;267750005;155205009;563001,Nystagmus,,,,H55.0,DOID:9650,pathologic nystagmus,C0028738,,MTHU000235,MONDO:0004843,pathologic nystagmus,Nystagmus and other irregular eye movements | Nystagmus | Nystagmus &/or other irregular eye movements | Nystagmus &/or other irregular eye movements (disorder) | Nystagmus | Congenital nystagmus | Nystagmus (& [congenital]) | Nystagmus (& [congenital]) (disorder) | Congenital nystagmus | Nystagmus | Nystagmus (& [congenital]) | Nystagmus (& [congenital]) (disorder) | Nystagmus | Nystagmus (disorder)
+BMGC_DS01753,BMG_DS002200,414916001;190963004;154776002;5476005,Obesity,Obesity,,,,DOID:9970,obesity,C0028754,D009765,MTHU000250,MONDO:0011122,obesity disorder,Obesity (disorder) | Obesity | Adiposis | Adiposity | Obesity | Obesity (disorder) | Adiposis | Adiposity | Simple obesity | Calorie overload | Adiposity (disorder)
+BMGC_DS01754,BMG_DS002201,190967003;238136002;389986000,Morbid obesity,,,,,DOID:11981,morbid obesity,C0028756,,MTHU051042,MONDO:0005139,morbid obesity,Morbid obesity | Morbid obesity (disorder)
+BMGC_DS01755,BMG_DS002202,,,,,,,DOID:10933,obsessive-compulsive disorder,C0028768,,164230,MONDO:0008114,obsessive-compulsive disorder,
+BMGC_DS01756,BMG_DS002203,,,,,,,DOID:10127,cerebral artery occlusion,C0028790,,,MONDO:0000944,cerebral artery occlusion,
+BMGC_DS01757,BMG_DS002204,,"Dermatitis, Occupational","Dermatitis, Occupational",,,,DOID:4404,occupational dermatitis,C0028796,D009783,,MONDO:0006589,occupational dermatitis,
+BMGC_DS01758,BMG_DS002205,,Occupational Diseases,Occupational Diseases,,,,,,C0028797,D009784,,MONDO:0100366,occupational disorder,
+BMGC_DS01759,BMG_DS002206,410042009;21924005,Ochronosis,Ochronosis,,,E70.29,DOID:14223,ochronosis,C0028817,D009794,,MONDO:0001910,ochronosis disorder,"Ochronosis due to homogentisate 1,2-dioxygenase deficiency (disorder) | Alcaptonuric ochronosis | Pigmentation due to alkaptonuria | Ochronosis | Alkaptonuric ochronosis | Ochronosis due to homogentisate 1,2-dioxygenase deficiency | Ochronosis due to alkaptonuria | Ochronosis | Alkaptonuric ochronosis | Ochronosis (disorder)"
+BMGC_DS01760,BMG_DS002207,,Ocular Hypertension,Ocular Hypertension,,,,DOID:9282,ocular hypertension,C0028840,D009798,,MONDO:0006875,ocular hypertension,
+BMGC_DS01761,BMG_DS002208,,Ocular Hypotension,Ocular Hypotension,,,,DOID:790,ocular hypotension,C0028841,D015814,,MONDO:0004390,ocular hypotension,
+BMGC_DS01762,BMG_DS002210,,Ocular Motility Disorders,Ocular Motility Disorders,,,,DOID:1279,ocular motility disease,C0028850,D015835,,MONDO:0001584,ocular motility disease,
+BMGC_DS01763,BMG_DS002211,,Ocular Torticollis,Ocular Motility Disorders,,,,,,C0028856,D015835,,,,
+BMGC_DS01764,BMG_DS002212,,Oculocerebrorenal Syndrome,Oculocerebrorenal Syndrome,,,,DOID:1056,oculocerebrorenal syndrome,C0028860,D009800,309000,MONDO:0010645,oculocerebrorenal syndrome,
+BMGC_DS01765,BMG_DS002213,,Oculomotor Nerve Paralysis,Oculomotor Nerve Diseases,,,,DOID:11550,oculomotor nerve paralysis,C0028866,D015840,,MONDO:0001309,oculomotor nerve paralysis,
+BMGC_DS01766,BMG_DS002217,22500005,Oesophagostomiasis,Oesophagostomiasis,,,,DOID:3983,oesophagostomiasis,C0028887,D009814,,MONDO:0005880,oesophagostomiasis,Oesophagostomiasis | Nodular worm disease | Infection by Oesophagostomum | Infection by Oesophagostomum (disorder)
+BMGC_DS01767,BMG_DS002218,,,,,,,,,C0028945,,,MONDO:0016695,oligodendroglioma,
+BMGC_DS01768,BMG_DS002219,,Oligospermia,Oligospermia,,,N46.1,DOID:14228,oligospermia,C0028960,D009845,,MONDO:0001913,oligospermia,
+BMGC_DS01769,BMG_DS002220,83128009;139461002,Oliguria,Oliguria,,,,,,C0028961,D009846,MTHU076561,,,Oliguria | Oliguria (finding) | Oligouria | Passes too little urine | Oliguria | Oliguria (finding)
+BMGC_DS01770,BMG_DS002221,,Olivopontocerebellar Atrophies,Olivopontocerebellar Atrophies,,,,DOID:14784,olivopontocerebellar atrophy,C0028968,D009849,,MONDO:0002017,olivopontocerebellar atrophy,
+BMGC_DS01771,BMG_DS002224,38539003,Onchocerciasis,Onchocerciasis,,,B73,DOID:11678,onchocerciasis,C0029001,D009855,,MONDO:0017137,onchocerciasis,Infection by Onchocerca volvulus | Onchocerciasis | Onchocercosis | Infection caused by Onchocerca volvulus (disorder) | Infection caused by Onchocerca volvulus
+BMGC_DS01772,BMG_DS002226,76047005;155968004;266648001,Oophoritis,Oophoritis,,,,DOID:10974,oophoritis,C0029051,D009869,,MONDO:0006877,oophoritis,Oophoritis | Oophoritis (disorder) | Inflammation of ovary | Pelvic inflammatory disease (& [chronic NOS] or [oophoritis] or [salpingitis]) | Chronic pelvic inflam. dis.NOS | Pelvic inflammatory disease | Salpingitis | Oophoritis | Inflam. dis.- pelvic | Pelvic inflammatory disease (& [chronic NOS] or [oophoritis] or [salpingitis]) (disorder) | Pelvic inflammatory disease (& [chronic NOS] or [oophoritis] or [salpingitis]) | Pelvic inflammatory disease | Inflam. dis.- pelvic | Chronic pelvic inflam. dis.NOS | Oophoritis | Salpingitis | Pelvic inflammatory disease (& [chronic NOS] or [oophoritis] or [salpingitis]) (disorder)
+BMGC_DS01773,BMG_DS002227,,,,,,,DOID:9699,ophthalmia neonatorum,C0029076,,,MONDO:0004854,ophthalmia neonatorum,
+BMGC_DS01774,BMG_DS002228,,"Ophthalmia, Sympathetic","Ophthalmia, Sympathetic",,,,DOID:12029,sympathetic ophthalmia,C0029077,D009879,,MONDO:0019198,sympathetic ophthalmia,
+BMGC_DS01775,BMG_DS002229,,,,,,,DOID:539,ophthalmoplegia,C0029089,,,MONDO:0003425,ophthalmoplegia,
+BMGC_DS01776,BMG_DS002230,,,,,,,DOID:11206,opioid abuse,C0029095,,,MONDO:0001225,opioid abuse,
+BMGC_DS01777,BMG_DS002231,1059007;187124006,Opisthorchiasis,Opisthorchiasis,1F84,Opisthorchiasis,B66.0,DOID:13768,opisthorchiasis,C0029106,D009889,,MONDO:0005884,opisthorchiasis,Opisthorchiasis | Cat liver fluke infection | Opisthorchiosis | Opisthorchiasis (disorder) | Opisthorchiasis (& [cat liver fluke infection]) | Cat liver fluke infection | Opisthorchiasis | Opisthorchiasis (& [cat liver fluke infection]) (disorder)
+BMGC_DS01778,BMG_DS002233,78999002,Opportunistic mycosis,,,,,DOID:2473,opportunistic mycosis,C0029119,,,MONDO:0002312,opportunistic mycosis,Opportunistic mycosis | Opportunistic mycosis (disorder)
+BMGC_DS01779,BMG_DS002234,,,,,,,,,C0029121,,,MONDO:0000495,oppositional defiant disorder,
+BMGC_DS01780,BMG_DS002235,,Optic Atrophy,Optic Atrophy,,,,DOID:5723,optic atrophy,C0029124,D009896,,MONDO:0003608,optic atrophy,
+BMGC_DS01781,BMG_DS002236,,"Optic Atrophies, Hereditary","Optic Atrophies, Hereditary",,,,,,C0029125,D015418,,MONDO:0043878,hereditary optic atrophy,
+BMGC_DS01782,BMG_DS002237,,Optic Disk Drusen,Optic Disk Drusen,,,,DOID:13561,optic disk drusen,C0029128,D015594,,MONDO:0001746,optic disk drusen,
+BMGC_DS01783,BMG_DS002238,77157004;194037001,Disorder of optic nerve,,,,,DOID:1891,optic nerve disease,C0029132,,,,,Disorder of optic nerve | Disorder of optic nerve (disorder) | Optic neuropathy | Disorders of optic nerve &/or visual pathways | Visual path disorder | Disorder of optic nerve | Optic nerve disorders | Disorders of the second nerve | Disorders of the IInd cranial nerve | Disorders of optic nerve and visual pathways | Disorders of optic nerve &/or visual pathways (disorder)
+BMGC_DS01784,BMG_DS002239,,Optic Neuritis,Optic Neuritis,,,,DOID:1210,optic neuritis,C0029134,D009902,,MONDO:0005885,optic neuritis,
+BMGC_DS01785,BMG_DS002240,,,,,,,DOID:5773,oral submucous fibrosis,C0029171,,,,,
+BMGC_DS01786,BMG_DS002241,,Oral Submucous Fibrosis,Oral Submucous Fibrosis,,,,DOID:5773,oral submucous fibrosis,C0029172,D009914,,MONDO:0018166,oral submucous fibrosis,
+BMGC_DS01787,BMG_DS002242,,Orbital Diseases,Orbital Diseases,,,,DOID:930,orbital disease,C0029182,D009916,,MONDO:0004751,disease of orbital part of eye adnexa,
+BMGC_DS01788,BMG_DS002243,,,,,,,DOID:4143,orbital cancer,C0029185,,,MONDO:0024611,orbit neoplasm,
+BMGC_DS01789,BMG_DS002244,367112009;29077001;197984006;274718005,Orchitis,Orchitis,,,N45.2,DOID:2518,orchitis,C0029191,D009920,,MONDO:0006882,orchitis,Orchitis | Orchitis (disorder) | Orchitis | Non-specific orchitis | Orchitis (disorder) | Inflammation of testis
+BMGC_DS01790,BMG_DS002245,40101002;2776000,Organic brain syndrome,,,,,,,C0029221,,,,,Organic brain syndrome | Organic brain syndrome (disorder) | Delirium | Organic brain syndrome | Acute confusional state | OBS - Organic brain syndrome | Acute psycho-organic syndrome | Acute organic reaction | ABS - Acute brain syndrome | Acute brain syndrome | Delirium (disorder)
+BMGC_DS01791,BMG_DS002246,,,,,,,DOID:1561,cognitive disorder,C0029227,,,,,
+BMGC_DS01792,BMG_DS002248,154369005;186653003;75116005,Psittacosis,Psittacosis,,,A70,DOID:11262,ornithosis,C0029291,D009956,,MONDO:0005888,ornithosis,Psittacosis | Psittacosis (disorder) | Ornithosis | Psittacosis | Parrot fever | Parrot fever due to Chlamydia psitacci | Ornithosis (disorder) | Chlamydia psittaci infection
+BMGC_DS01793,BMG_DS002249,,Orofaciodigital Syndromes,Orofaciodigital Syndromes,,,,DOID:0060316;DOID:4501,orofaciodigital syndrome I | orofaciodigital syndrome,C0029294,D009958,,MONDO:0015375,orofaciodigital syndrome,
+BMGC_DS01794,BMG_DS002250,,,,,,,,,C0029295,,,MONDO:0021364,neoplasm of oropharynx,
+BMGC_DS01795,BMG_DS002252,,Orthomyxoviridae Infections,Orthomyxoviridae Infections,,,,,,C0029342,D009976,,,,
+BMGC_DS01796,BMG_DS002253,72047008,Juvenile osteochondrosis of tibial tubercle,,,,,DOID:7489,Osgood-Schlatter's disease,C0029376,,,MONDO:0004241,Osgood-Schlatter disease,Juvenile osteochondrosis of tibial tubercle | Osgood-Schlatter's disease | Juvenile osteochondrosis of tibial tubercle (disorder) | Osgood Schlatter disease | Osgood Schlatters disease
+BMGC_DS01797,BMG_DS002254,274144001;44462005,Osteitis,Osteitis,,,,DOID:3342,bone inflammation disease,C0029400,D010000,,MONDO:0002614,bone inflammation disease,Bone inflammatory disease | Bone inflammatory disease (disorder) | Osteitis | Inflammation of bone | Inflammatory disorder of bone | Osteitis | Inflammation of bone | Osteitis (disorder)
+BMGC_DS01798,BMG_DS002255,,Osteitis Deformans,Osteitis Deformans,,,,DOID:5408,Paget's disease of bone,C0029401,D010001,,MONDO:0005382,bone Paget disease,
+BMGC_DS01799,BMG_DS002256,,Osteitis Fibrosa Cystica,Osteitis Fibrosa Cystica,,,,DOID:3341,osteitis fibrosa,C0029405,D010002,,MONDO:0005890,osteitis fibrosa,
+BMGC_DS01800,BMG_DS002257,80843008;396275006;267888004;225655006,Degenerative polyarthritis,,,,,,,C0029408,,,MONDO:0005178,osteoarthritis,Degenerative joint disease | Osteoarthrosis | Degenerative arthritis | Degenerative polyarthritis | Hypertrophic arthritis | Hypertrophic polyarthritis | Osteoarthritis | Proliferative arthritis | Degenerative arthropathy | Degenerative joint disease (disorder) | Osteoarthritis (disorder) | Osteoarthritis | OA - Osteoarthritis | Degenerative arthritis | OA - Osteoarthrosis | Hypertrophic arthritis | Degenerative joint disease | Hypertrophic polyarthritis | Osteoarthrosis | Degenerative arthropathy | Osteoarthritis deformans | Osteoarthrosis deformans | Osteoarthritis | Degenerative arthritis | OA - Osteoarthritis | Osteoarthrosis | OA - Osteoarthrosis | Osteoarthritis (disorder) | Degenerative arthropathy | Hypertrophic polyarthritis | Proliferative arthritis | Hypertrophic arthritis | Degenerative polyarthritis | Degenerative joint disease | Degenerative polyarthritis | Degenerative polyarthritis (disorder)
+BMGC_DS01801,BMG_DS002258,239872002;156492009,Osteoarthritis of hip,,,,M16,,,C0029410,,,MONDO:0006629,"osteoarthritis, hip",OA - Osteoarthritis of hip | Osteoarthritis of hip | Osteoarthritis of hip (disorder) | Degenerative joint disease of hip | Coxae malum senilis | Osteoarthritis of hip | Osteoarthritis of hip (disorder)
+BMGC_DS01802,BMG_DS002259,,"Osteoarthropathy, Primary Hypertrophic","Osteoarthropathy, Primary Hypertrophic",,,,DOID:14283,primary hypertrophic osteoarthropathy,C0029411,D010004,,MONDO:0016620,primary hypertrophic osteoarthropathy,
+BMGC_DS01803,BMG_DS002260,,"Osteoarthropathy, Secondary Hypertrophic","Osteoarthropathy, Secondary Hypertrophic",,,,DOID:10393,secondary hypertrophic osteoarthropathy,C0029412,D010005,,MONDO:0006965,secondary hypertrophic osteoarthropathy,
+BMGC_DS01804,BMG_DS002263,,Osteochondritis Dissecans,Osteochondritis Dissecans,,,,DOID:84,osteochondritis dissecans,C0029421,D010008,,MONDO:0017178,osteochondritis dissecans,
+BMGC_DS01805,BMG_DS002264,,Osteochondrodysplasias,Osteochondrodysplasias,,,,DOID:2256,osteochondrodysplasia,C0029422,D010009,,MONDO:0005516,osteochondrodysplasia,
+BMGC_DS01806,BMG_DS002266,65477003;19579005,Osteochondrosis,Osteochondrosis,,,,DOID:8125,osteochondrosis,C0029429,D055034,,MONDO:0018381,osteochondrosis,Osteochondrosis | Osteochondrosis (disorder) | Juvenile osteochondritis | Juvenile osteochondrosis | Osteochondrosis | Osteochondritis juvenilis | Osteochondropathy-juven | Juvenile osteochondritis (disorder)
+BMGC_DS01807,BMG_DS002267,,Osteogenesis Imperfecta,Osteogenesis Imperfecta,,,,DOID:12347,osteogenesis imperfecta,C0029434,D010013,,MONDO:0019019,osteogenesis imperfecta,
+BMGC_DS01808,BMG_DS002268,,"Osteolysis, Essential","Osteolysis, Essential",,,,DOID:4837,Gorham's disease,C0029436,D010015,,MONDO:0003157,disappearing bone disease,
+BMGC_DS01809,BMG_DS002270,,Massive Osteolyses,"Osteolysis, Essential",,,,,,C0029438,D010015,123880,MONDO:0007414,Gorham-Stout disease,
+BMGC_DS01810,BMG_DS002273,4598005;190639009;154728003,Osteomalacia,,,,,DOID:10573,osteomalacia,C0029442,,MTHU007357,MONDO:0001068,osteomalacia,Osteomalacia | Osteomalacia (disorder) | OM - osteomalacia | Vitamin D deficiency | Osteomalacia | Rickets | (Vitamin D deficiency) or (osteomalacia) or (rickets) | (Vitamin D deficiency) or (osteomalacia) or (rickets) (disorder) | Osteomalacia | Vitamin D deficiency | Rickets | (Vitamin D deficiency) or (osteomalacia) or (rickets) | (Vitamin D deficiency) or (osteomalacia) or (rickets) (disorder)
+BMGC_DS01811,BMG_DS002274,240141009;60168000,Osteomyelitis,Osteomyelitis,,,M86,,,C0029443,D010019,MTHU037798,MONDO:0005246,osteomyelitis,Osteomyelitis | Osteomyelitis (disorder) | Osteomyelitis | Pyogenic inflammation of bone | OSTM - Osteomyelitis | OM - Osteomyelitis | Osteomyelitis (disorder)
+BMGC_DS01812,BMG_DS002275,,,,,,,DOID:10159,osteonecrosis,C0029445,,,MONDO:0005380,osteonecrosis,
+BMGC_DS01813,BMG_DS002276,203889002;156879002;312894000;78441005,Osteopenia,"Bone Diseases, Metabolic",,,,,,C0029453,D001851,MTHU000031,,,Osteopenia | Osteopenia (disorder) | Osteopenia | Osteopenia (disorder) | Bone loss | Osteopenia | Osteopenia (morphologic abnormality)
+BMGC_DS01814,BMG_DS002277,205500005;1926006,Osteopetrosis,Osteopetrosis,LD24.10,Osteopetrosis,Q78.2,DOID:0110946;DOID:13533,autosomal recessive osteopetrosis 7 | osteopetrosis,C0029454,D010022,MTHU056843,MONDO:0017198,osteopetrosis,Osteopetrosis | Osteopetrosis (disorder)
+BMGC_DS01815,BMG_DS002278,9147009,Osteopoikilosis (disorder),,,,,DOID:11991,osteopoikilosis,C0029455,,,MONDO:0001414,osteopoikilosis,Osteopoikilosis | Osteopoikilosis (disorder) | Buschke-Ollendorff syndrome
+BMGC_DS01816,BMG_DS002279,156825006;64859006,Osteoporosis,Osteoporosis,,,,DOID:11476,osteoporosis,C0029456,D010024,166710;MTHU002380,MONDO:0005298,osteoporosis,Osteoporosis | Osteoporosis (disorder)
+BMGC_DS01817,BMG_DS002280,,"Osteoporosis, Postmenopausal","Osteoporosis, Postmenopausal",,,,,,C0029458,D015663,,MONDO:0008159,postmenopausal osteoporosis,
+BMGC_DS01818,BMG_DS002281,,"Osteoporosis, Senile",Osteoporosis,,,,,,C0029459,D010024,,,,
+BMGC_DS01819,BMG_DS002283,,,,,,,DOID:3347,osteosarcoma,C0029463,,,MONDO:0009807,osteosarcoma,
+BMGC_DS01820,BMG_DS002284,49347007,Osteosclerosis,Osteosclerosis,,,,DOID:4254,osteosclerosis,C0029464,D010026,MTHU005522,MONDO:0002933,osteosclerosis,Osteosclerosis | Osteosclerosis (disorder)
+BMGC_DS01821,BMG_DS002285,,Ostertagiasis,Ostertagiasis,,,,DOID:3985,ostertagiasis,C0029471,D010029,,MONDO:0005891,ostertagiasis,
+BMGC_DS01822,BMG_DS002287,201213005,Other acne,,,,L70.8,DOID:9098,sebaceous gland disease,C0029485,,,,,Other acne | Other acne (disorder)
+BMGC_DS01823,BMG_DS002288,,,,,,,DOID:6088,acute stress disorder,C0029488,,,,,
+BMGC_DS01824,BMG_DS002289,,,,,,,DOID:53,pituitary gland disease,C0029493,,,,,
+BMGC_DS01825,BMG_DS002291,,,,,,,DOID:0060186;DOID:0060187,diversion colitis | chemical colitis,C0029512,,,,,
+BMGC_DS01826,BMG_DS002292,,,,,,,DOID:5119,ovarian cyst,C0029513,,,,,
+BMGC_DS01827,BMG_DS002293,,,,,,,DOID:2468,psychotic disorder,C0029516,,,,,
+BMGC_DS01828,BMG_DS002298,193620000,Other cataract,,,,H26,DOID:83,cataract,C0029531,,,,,Other cataract | Other cataract (disorder)
+BMGC_DS01829,BMG_DS002301,,Other chorea,,8A0Z,"Movement disorders, unspecified",G25.5,DOID:12859;DOID:0060810,syndromic X-linked intellectual disability type 10 | choreatic disease,C0029542,,,,,
+BMGC_DS01830,BMG_DS002309,201095006,Other dermatoses,,,,,DOID:37,skin disease,C0029574,,,,,Other dermatoses | Other dermatoses (disorder)
+BMGC_DS01831,BMG_DS002310,,,,,,,DOID:0050161;DOID:974,lower respiratory tract disease | upper respiratory tract disease,C0029581,,,,,
+BMGC_DS01832,BMG_DS002311,155603009;196057004,Other respiratory system diseases,,,,,DOID:1579,respiratory system disease,C0029582,,,,,Other respiratory system diseases | Other respiratory system diseases (disorder)
+BMGC_DS01833,BMG_DS002312,,Other disorders of lens,,,,H27,,,C0029590,,,,,
+BMGC_DS01834,BMG_DS002313,154744007;190798009,Other disorders of lipoid metabolism,,,,,DOID:9455,lipid storage disease,C0029591,,,,,Other disorders of lipoid metabolism | Other disorders of lipoid metabolism (disorder)
+BMGC_DS01835,BMG_DS002315,,,,,,,DOID:2345,plasma protein metabolism disease,C0029594,,,,,
+BMGC_DS01836,BMG_DS002316,190917005;267450006,Other disorders of purine and pyrimidine metabolism,,5C55.Z,"Inborn errors of purine, pyrimidine or nucleotide metabolism, unspecified",E79.8,DOID:653,purine-pyrimidine metabolic disorder,C0029595,,,,,Disorders of purine and pyrimidine metabolism: [Lesch-Nyhan syndrome] or [other] | Other disorders of purine and pyrimidine metabolism | Lesch-Nyhan syndrome | Lesch - Nyhan syndrome | Disorders of purine and pyrimidine metabolism: [Lesch-Nyhan syndrome] or [other] (disorder) | Other disorders of purine and pyrimidine metabolism | Other disorders of purine and pyrimidine metabolism (disorder)
+BMGC_DS01837,BMG_DS002317,195962007,Other emphysema,,CA21.Z,"Emphysema, unspecified",J43.8,DOID:9675,pulmonary emphysema,C0029607,,,,,Other emphysema | Other emphysema (morphologic abnormality)
+BMGC_DS01838,BMG_DS002321,,,,,,,DOID:10273,heart conduction disease,C0029630,,,,,
+BMGC_DS01839,BMG_DS002325,,Other impaction of intestine,,DE2Z,"Diseases of the digestive system, unspecified",K56.49;K56.4,DOID:8448,intestinal impaction,C0029640,,,,,
+BMGC_DS01840,BMG_DS002326,202651004,Other inflammatory spondylopathies,,,,M46,DOID:6590,spondylitis,C0029644,,,,,Other inflammatory spondylopathies | Other inflammatory spondylopathies (disorder)
+BMGC_DS01841,BMG_DS002328,,Other localized visual field defect,,,,H53.45,DOID:9335,scotoma,C0029657,,,,,
+BMGC_DS01842,BMG_DS002332,,Other mucopurulent conjunctivitis,,,,H10.02,DOID:11184,acute conjunctivitis,C0029668,,,,,
+BMGC_DS01843,BMG_DS002337,,,,,,,DOID:12185,otosclerosis,C0029696,,,,,
+BMGC_DS01844,BMG_DS002338,190543001;267399006,Other ovarian failure,,,,,DOID:1414,ovarian dysfunction,C0029697,,,,,(Other ovarian failure) or (ovarian hypogonadism) | Ovarian hypogonadism | Other ovarian failure | (Other ovarian failure) or (ovarian hypogonadism) (disorder) | Other ovarian failure | Other ovarian failure (disorder)
+BMGC_DS01845,BMG_DS002339,,Other peripheral vertigo,,AB34.1,Other peripheral vertigo,H81.3;H81.39,DOID:9847,peripheral vertigo,C0029706,,,,,
+BMGC_DS01846,BMG_DS002340,,,,,,,DOID:1510,personality disorder,C0029707,,,,,
+BMGC_DS01847,BMG_DS002344,111823001,Other specified cardiovascular syphilis,,,,,DOID:9880,cardiovascular syphilis,C0029751,,,,,Other specified cardiovascular syphilis | Other specified cardiovascular syphilis (disorder)
+BMGC_DS01848,BMG_DS002345,,,,,,,DOID:1829,urethral stricture,C0029752,,,,,
+BMGC_DS01849,BMG_DS002350,,Other specified diseases of hard tissues of teeth,,DA08.1,Certain specified diseases of hard tissues of teeth,K03.89;K03.8,DOID:214,teeth hard tissue disease,C0029770,,,,,
+BMGC_DS01850,BMG_DS002351,,Other specified diseases of pancreas,,DC3Z,"Diseases of pancreas, unspecified",K86.8;K86.89,DOID:26,pancreas disease,C0029771,,,,,
+BMGC_DS01851,BMG_DS002353,,,,,,,DOID:10854,salivary gland disease,C0029773,,,,,
+BMGC_DS01852,BMG_DS002358,,Other specified disorders of penis,,GB06.Z,"Disorders of penis, unspecified",N48.8;N48.89,DOID:1529,penile disease,C0029785,,,,,
+BMGC_DS01853,BMG_DS002361,,,,,,,DOID:9974,drug dependence,C0029792,,,,,
+BMGC_DS01854,BMG_DS002365,,,,,,,DOID:10247,pleurisy,C0029799,,,,,
+BMGC_DS01855,BMG_DS002366,196737009,Other specified gastritis,,,,,DOID:8644,gastroduodenitis,C0029800,,,,,Other specified gastritis | Other specified gastritis (disorder)
+BMGC_DS01856,BMG_DS002367,,,,,,,DOID:1284,prolapse of female genital organ,C0029801,,,,,
+BMGC_DS01857,BMG_DS002370,154828005;191328005,Other specified hemorrhagic conditions,,3B4Z,"Coagulation defects, unspecified",D69.8,DOID:0111045;DOID:0111056;DOID:0060692;DOID:0111057,platelet-type bleeding disorder 8 | platelet-type bleeding disorder 3 | platelet-type bleeding disorder 9 | platelet-type bleeding disorder 11,C0029804,,,,,Other specified haemorrhagic conditions | Other specified hemorrhagic conditions | Other specified haemorrhagic conditions (disorder) | Other specified hemorrhagic conditions | Other specified haemorrhagic conditions | Other specified hemorrhagic conditions (disorder)
+BMGC_DS01858,BMG_DS002371,,,,,,,DOID:0060344,acrodermatitis chronica atrophicans,C0029805,,,,,
+BMGC_DS01859,BMG_DS002373,,,,,,,DOID:11758,iron deficiency anemia,C0029810,,,,,
+BMGC_DS01860,BMG_DS002379,197183001,Other specified peritonitis,,,,,DOID:8283,peritonitis,C0029823,,,,,Other specified peritonitis | Other specified peritonitis (disorder)
+BMGC_DS01861,BMG_DS002381,187116001,Other specified schistosomiasis,,,,,DOID:1395,schistosomiasis,C0029827,,,,,Other specified schistosomiasis | Other specified schistosomiasis (disorder)
+BMGC_DS01862,BMG_DS002383,194125000,Other specified strabismus,,9C8Y,Other specified strabismus or ocular motility disorders,H50.8;H50.89,DOID:540,strabismus,C0029831,,,,,Other specified strabismus | Other specified strabismus (disorder)
+BMGC_DS01863,BMG_DS002384,,,,,,,DOID:561,trigeminal nerve disease,C0029834,,,,,
+BMGC_DS01864,BMG_DS002385,186298002;111834003,Other specified tularemia,,,,,DOID:14239;DOID:2123,gastrointestinal tularemia | tularemia,C0029835,,,,,Other specified tularaemia | Other specified tularemia | Other specified tularemia (disorder) | Other specified tularemia | Other specified tularemia (disorder)
+BMGC_DS01865,BMG_DS002386,267817001;201267004,Other specified urticaria,,,,,DOID:1555,urticaria,C0029839,,,,,Other specified urticaria | Other specified urticaria (disorder) | (Other specified urticaria) or (nettle rash) | Nettle rash | Other specified urticaria | (Other specified urticaria) or (nettle rash) (disorder)
+BMGC_DS01866,BMG_DS002388,186577001,Other specified viral exanthemata,,,,,DOID:8672,viral exanthem,C0029841,,,,,Other specified viral exanthemata | Other specified viral exanthemata (disorder)
+BMGC_DS01867,BMG_DS002391,196103008,Other spontaneous pneumothorax,,CB21.1,Other spontaneous pneumothorax,J93.1,DOID:1673,pneumothorax,C0029850,,,,,Other spontaneous pneumothorax | Other spontaneous pneumothorax (disorder)
+BMGC_DS01868,BMG_DS002394,,,,,,,DOID:5199,ureteral obstruction,C0029866,,,,,
+BMGC_DS01869,BMG_DS002397,194154006,Other vitreous opacities,,9B84,"Vitreous opacities, membranes or strands",H43.3;H43.39,DOID:9720,vitreous disease,C0029872,,,,,Other vitreous opacities | Other vitreous opacities (disorder)
+BMGC_DS01870,BMG_DS002398,,Ear Inflammation,Otitis,,,,,,C0029877,D010031,,,,
+BMGC_DS01871,BMG_DS002399,,Otitis Externa,Otitis Externa,,,,,,C0029878,D010032,,MONDO:0004795,otitis externa,
+BMGC_DS01872,BMG_DS002400,,Otitis Media,Otitis Media,,,,DOID:10754,otitis media,C0029882,D010033,,MONDO:0005441,otitis media,
+BMGC_DS01873,BMG_DS002401,,Otitis Media with Effusion,Otitis Media with Effusion,,,,,,C0029883,D010034,,,,
+BMGC_DS01874,BMG_DS002402,39288006;267758003,Suppurative otitis media,,,,,DOID:11506,suppurative otitis media,C0029888,,,MONDO:0005975,suppurative otitis media,"Purulent otitis media | Suppurative otitis media | Purulent otitis media (disorder) | Suppurative otitis media &/or ([left] or [right]) &/or purulent otitis media | Purulent otitis media | Otitis media, suppurative | Suppurative otitis med. | Suppurative otitis media | Right otitis media - supp | Left otitis media - supp | Otitis media - purulent | Suppurative otitis media &/or ([left] or [right]) &/or purulent otitis media (disorder)"
+BMGC_DS01875,BMG_DS002403,275479004;53316003,Otomycosis,Otomycosis,,,,DOID:0050147,otomycosis,C0029895,D059249,,MONDO:0000262,otomycosis,Otomycosis | Otomycosis (disorder) | Otomycosis | Otomycosis (disorder) | Otitis mycotic externa
+BMGC_DS01876,BMG_DS002406,,Ovarian Cysts,Ovarian Cysts,,,,,,C0029927,D010048,,MONDO:0003282,ovarian cyst,
+BMGC_DS01877,BMG_DS002407,,Ovarian Diseases,Ovarian Diseases,,,,DOID:1100,ovarian disease,C0029928,D010049,,,,
+BMGC_DS01878,BMG_DS002409,266162007;187178006;266222003;154415009;19722001,Oxyuriasis,Oxyuriasis,,,,DOID:7457,enterobiasis,C0030100,D010123,,,,Enterobiasis | Oxyuriasis | Pinworm disease | Enterobiasis - threadworm | Pinworm infection | Threadworm infection | Enterobiosis | Enterobiasis (disorder) | (Threadworm enterobiasis) or (oxyuriasis) or (pinworm) | Enterobiasis - threadworm | Pinworm | Oxyuriasis | (Threadworm enterobiasis) or (oxyuriasis) or (pinworm) (disorder) | (Other helminthiases (& [oxyuriasis] or [schistosomiasis] or [taenia infestation] or [trichinosis])) or ([filaria] or [flukes] or [tapeworms] or [toxocara]) | Oxyuriasis | Filaria | Toxocara | Other helminthiases | Trichinosis | Schistosomiasis | Taenia infestation | Flukes | Tapeworms | (Other helminthiases (& [oxyuriasis] or [schistosomiasis] or [taenia infestation] or [trichinosis])) or ([filaria] or [flukes] or [tapeworms] or [toxocara]) (disorder) | (Other helminthiases (& [oxyuriasis] or [schistosomiasis] or [taenia infestation] or [trichinosis])) or ([filaria] or [flukes] or [tapeworms] or [toxocara]) | Oxyuriasis | Tapeworms | Taenia infestation | Flukes | Other helminthiases | Filaria | Schistosomiasis | Trichinosis | Toxocara | (Other helminthiases (& [oxyuriasis] or [schistosomiasis] or [taenia infestation] or [trichinosis])) or ([filaria] or [flukes] or [tapeworms] or [toxocara]) (disorder) | Infection by Enterobius vermicularis | Infection by Enterobius vermicularis (disorder)
+BMGC_DS01879,BMG_DS002411,25822001,Pachymeningitis,Meningitis,,,,,,C0030167,D008581,,,,Pachymeningitis | Pachymeningitis (disorder)
+BMGC_DS01880,BMG_DS002413,,,,,,,,,C0030186,,167300,MONDO:0008177,extramammary Paget disease,
+BMGC_DS01881,BMG_DS002415,,Pustulosis of Palms and Soles,Psoriasis,,,,DOID:4398,pustulosis of palm and sole,C0030246,D011565,,MONDO:0015597,pustulosis palmaris et plantaris,
+BMGC_DS01882,BMG_DS002417,,,,,,,DOID:8007,Pancoast tumor,C0030271,,,MONDO:0024674,Pancoast syndrome,
+BMGC_DS01883,BMG_DS002418,,Pancreatic Cyst,Pancreatic Cyst,,,,,,C0030283,D010181,,,,
+BMGC_DS01884,BMG_DS002419,,Pancreatic Diseases,Pancreatic Diseases,,,,,,C0030286,D010182,,MONDO:0002356,pancreas disorder,
+BMGC_DS01885,BMG_DS002420,,Pancreatic Fistula,Pancreatic Fistula,,,,,,C0030290,D010185,,,,
+BMGC_DS01886,BMG_DS002421,,,,,,,DOID:1793,pancreatic cancer,C0030297,,,MONDO:0021040,pancreatic neoplasm,
+BMGC_DS01887,BMG_DS002422,,Pancreatic Pseudocyst,Pancreatic Pseudocyst,,,,,,C0030299,D010192,,,,
+BMGC_DS01888,BMG_DS002423,75694006;197461009;393591004,Pancreatitis,Pancreatitis,,,,DOID:4989,pancreatitis,C0030305,D010195,MTHU003881,MONDO:0004982,pancreatitis,Pancreatitis | Pancreatitis (disorder) | Inflammation of pancreas | Pancreatitis (& [acute NOS]) | Pancreatitis | Acute pancreatitis NOS | Pancreatitis (& [acute NOS]) (disorder) | Pancreatitis | Pancreatitis (disorder)
+BMGC_DS01889,BMG_DS002424,127034005,Pancytopenia,Pancytopenia,,,D61.81,DOID:12450,pancytopenia,C0030312,D010198,MTHU036683,MONDO:0001529,pancytopenia,Pancytopenia | Pancytopenia (disorder)
+BMGC_DS01890,BMG_DS002425,,,,,,,DOID:594,panic disorder,C0030319,,,MONDO:0005383,panic disorder,
+BMGC_DS01891,BMG_DS002426,22125009;156779007;268122002,Panniculitis,Panniculitis,,,,DOID:1526,panniculitis,C0030326,D015434,MTHU032395,MONDO:0006591,panniculitis,Panniculitis | Panniculitis (disorder) | Panniculitis | Nonarticular rheumatism NOS | (Nonarticular rheumatism NOS) or (panniculitis) | (Nonarticular rheumatism NOS) or (panniculitis) (disorder) | (Nonarticular rheumatism NOS) or (panniculitis) | Nonarticular rheumatism NOS | Panniculitis | (Nonarticular rheumatism NOS) or (panniculitis) (disorder)
+BMGC_DS01892,BMG_DS002428,,"Panniculitis, Nodular Nonsuppurative","Panniculitis, Nodular Nonsuppurative",,,,DOID:1525,nodular nonsuppurative panniculitis,C0030328,D010201,,MONDO:0018063,nodular non-suppurative panniculitis,
+BMGC_DS01893,BMG_DS002430,,"Panniculitis, Subacute Nodular Migratory",Panniculitis,,,,,,C0030331,D015434,,,,
+BMGC_DS01894,BMG_DS002431,33382000,Panophthalmitis,Panophthalmitis,,,,DOID:13732,panophthalmitis,C0030332,D010202,,MONDO:0006884,panophthalmitis,Panophthalmitis | Panophthalmitis (disorder)
+BMGC_DS01895,BMG_DS002432,75614007,Panuveitis,Panuveitis,,,H44.11,DOID:12030,panuveitis,C0030343,D015864,MTHU068572,MONDO:0017255,panuveitis,Panuveitis | Panuveitis (disorder) | Diffuse uveitis
+BMGC_DS01896,BMG_DS002433,423488006;111526001;155187009;423341008,Papilledema,Papilledema,9C40.A0,Papilloedema,H47.1,DOID:146;DOID:10175,papilledema | optic papillitis,C0030353,D010211,MTHU007182,MONDO:0006879,optic papillitis,Papilledema - optic disc edema due to raised intracranial pressure (disorder) | Papilloedema - optic disc oedema due to raised intracranial pressure | Papilledema - optic disc edema due to raised intracranial pressure | Papilloedema due to raised intracranial pressure | Papilledema due to raised intracranial pressure | Papilledema | Papilloedema | Choked disc | Choked disk | Blurring of optic disk | Papilledema (disorder) | Optic disc oedema | Optic disc edema | Papilloedema | Papilledema | Papilloedema (disorder) | Optic disc edema | Optic disc oedema | Edema of optic disc (disorder) | Edema of optic disc
+BMGC_DS01897,BMG_DS002434,,,,,,,DOID:2615,papilloma,C0030354,,,MONDO:0002363,papilloma,
+BMGC_DS01898,BMG_DS002435,,Papillon-Lefevre Disease,Papillon-Lefevre Disease,,,,DOID:3389,Papillon-Lefevre disease,C0030360,D010214,245000,MONDO:0009490,Papillon-Lefevre disease,
+BMGC_DS01899,BMG_DS002437,,Phlebotomus Fever,Phlebotomus Fever,,,,DOID:11360,Phlebotomus fever,C0030372,D010217,,MONDO:0005913,phlebotomus fever,
+BMGC_DS01900,BMG_DS002439,59925007,Paracoccidioidomycosis,Paracoccidioidomycosis,,,B41,DOID:12662,paracoccidioidomycosis,C0030409,D010229,,MONDO:0005894,paracoccidioidomycosis,Paracoccidioidomycosis | South American blastomycosis | Infection by Blastomyces brasiliensis | Infection by Paracoccidioides brasiliensis | Brazilian blastomycosis | Lutz-Splendore-Almeida disease | Paracoccidioidomycosis (disorder)
+BMGC_DS01901,BMG_DS002440,,,,,,,DOID:0050773,paraganglioma,C0030421,,,MONDO:0000448,paraganglioma,
+BMGC_DS01902,BMG_DS002441,30369007,Paragonimiasis,Paragonimiasis,1F85,Paragonimiasis,B66.4,DOID:10699,paragonimiasis,C0030424,D010237,,MONDO:0005895,paragonimiasis,Infection by Paragonimus | Paragonimiasis | Oriental lung fluke disease | Pulmonary distomiasis | Paragonimosis | Pulmonary distomatosis | Lung fluke infection | Lung fluke disease | Pulmonary paragonimiasis | Endemic oriental haemoptysis | Endemic oriental hemoptysis | Infection caused by Paragonimus (disorder) | Infection caused by Paragonimus
+BMGC_DS01903,BMG_DS002442,65068000;200766001,Parakeratosis,Parakeratosis,,,,,,C0030436,D010241,MTHU002999,,,Parakeratosis | Parakeratosis (morphologic abnormality) | Parakeratosis | Parakeratosis (disorder)
+BMGC_DS01904,BMG_DS002443,,Parakeratosis Variegata,Parapsoriasis,,,,,,C0030437,D010267,,,,
+BMGC_DS01905,BMG_DS002444,54304004,Progressive bulbar palsy,,,,G12.22,DOID:681,progressive bulbar palsy,C0030442,,,MONDO:0008890,progressive bulbar palsy,Progressive bulbar palsy | Bulbar paralysis | Bulbar palsy | PBP - Progressive bulbar palsy | Progressive bulbar palsy (disorder)
+BMGC_DS01906,BMG_DS002445,,Familial Periodic Paralysis,"Paralyses, Familial Periodic",,,,DOID:1029,familial periodic paralysis,C0030443,D010245,,MONDO:0000995,familial periodic paralysis,
+BMGC_DS01907,BMG_DS002446,,Paralytic Ileus,Intestinal Pseudo-Obstruction,,,,DOID:8442,paralytic ileus,C0030446,D007418,,MONDO:0004568,paralytic ileus,
+BMGC_DS01908,BMG_DS002447,280483007;37518008,Parametritis,Parametritis,,,,DOID:1260,parametritis,C0030455,D010249,,MONDO:0006887,parametritis,Parametritis | Parametritis (disorder) | Inflammatory disease of female pelvic organs AND/OR tissues | Inflammatory disease of female pelvic organs AND/OR tissues (disorder)
+BMGC_DS01909,BMG_DS002449,,,,,,,DOID:1352,paranasal sinus disease,C0030469,,,MONDO:0001735,paranasal sinus disorder,
+BMGC_DS01910,BMG_DS002450,,,,,,,DOID:1350,paranasal sinus benign neoplasm,C0030470,,,MONDO:0005289,paranasal sinus neoplasm,
+BMGC_DS01911,BMG_DS002451,,,,,,,,,C0030472,,,MONDO:0021073,paraneoplastic syndrome,
+BMGC_DS01912,BMG_DS002452,,,,,,,DOID:10938,paranoid personality disorder,C0030477,,,MONDO:0001163,paranoid personality disorder,
+BMGC_DS01913,BMG_DS002453,,Tropical Spastic Paraparesis,"Paraparesis, Tropical Spastic",,,,DOID:321,tropical spastic paraparesis,C0030481,D015493,159580,MONDO:0008039,tropical spastic paraparesis,
+BMGC_DS01914,BMG_DS002455,155922002;13758004,Paraphimosis,Paraphimosis,,,N47.2,DOID:5334,paraphimosis,C0030483,D010263,,MONDO:0006889,paraphimosis,Paraphimosis | Paraphimosis (disorder)
+BMGC_DS01915,BMG_DS002456,155031004;60389000,Paraplegia,Paraplegia,MB56,Paraplegia,G82.2,DOID:607,paraplegia,C0030486,D010264,MTHU036387,MONDO:0003757,paraplegia,Paraplegia | Paraplegia (disorder) | Paraplegia | Paralysis of both lower limbs | Lower paraplegia | Paraplegia (disorder) | Paraplegia (complete or partial paralysis of legs)
+BMGC_DS01916,BMG_DS002458,267851002;88233000;200979001;156371008,Parapsoriasis,Parapsoriasis,,,L41,DOID:9088,parapsoriasis,C0030491,D010267,,MONDO:0006592,parapsoriasis,(Psoriasis NOS) or (guttate psoriasis) or (parapsoriasis) | Psoriasis NOS | Guttate psoriasis | Parapsoriasis | (Psoriasis NOS) or (guttate psoriasis) or (parapsoriasis) (disorder) | Parapsoriasis | Parapsoriasis (disorder) | (Psoriasis NOS) or (guttate psoriasis) or (parapsoriasis) | Guttate psoriasis | Psoriasis NOS | Parapsoriasis | (Psoriasis NOS) or (guttate psoriasis) or (parapsoriasis) (disorder)
+BMGC_DS01917,BMG_DS002459,,Parasitic Diseases,Parasitic Diseases,,,,,,C0030499,D010272,,MONDO:0005135,parasitic infectious disease,
+BMGC_DS01918,BMG_DS002460,,"Parasitic Diseases, Animal","Parasitic Diseases, Animal",,,,,,C0030500,D010273,,MONDO:0024969,"parasitic disease, non-human animal",
+BMGC_DS01919,BMG_DS002461,58690002,Parasomnia,Parasomnias,,,G47.5,,,C0030508,D020447,MTHU053515,,,Parasomnia | Parasomnia (disorder) | Parasomnia (sleep disorder)
+BMGC_DS01920,BMG_DS002462,,Parathyroid Diseases,Parathyroid Diseases,,,,DOID:11201,parathyroid gland disease,C0030517,D010279,,,,
+BMGC_DS01921,BMG_DS002463,,,,,,,DOID:1540,parathyroid carcinoma,C0030521,,,MONDO:0021360,tumor of parathyroid gland,
+BMGC_DS01922,BMG_DS002464,12223006,Paratuberculosis,Paratuberculosis,,,,,,C0030524,D010283,,MONDO:0025449,paratuberculosis,Johne's disease | Paratuberculosis | Johne's disease (disorder) | Johne disease
+BMGC_DS01923,BMG_DS002465,,Paratyphoid Fever,Paratyphoid Fever,,,,DOID:3055,paratyphoid fever,C0030528,D010284,,MONDO:0018626,paratyphoid fever,
+BMGC_DS01924,BMG_DS002466,26544005,Paresis,Paresis,,,,,,C0030552,D010291,MTHU074509,,,Muscle weakness | Muscle weakness (finding) | Muscle strength reduced | Decreased muscle strength
+BMGC_DS01925,BMG_DS002467,91019004,Paresthesia,Paresthesia,,,,,,C0030554,D010292,MTHU016084,,,Paresthesia | Paraesthesia | Paresthesia (finding) | Paraesthesia (numbness/tingling) | Paresthesia (numbness/tingling)
+BMGC_DS01926,BMG_DS002468,,Parkinson Disease,Parkinson Disease,,,,DOID:14330,Parkinson's disease,C0030567,D010300,,MONDO:0005180,Parkinson disease,
+BMGC_DS01927,BMG_DS002469,,"Parkinson Disease, Postencephalitic","Parkinson Disease, Postencephalitic",,,,DOID:14332,postencephalitic Parkinson disease,C0030568,D010301,,MONDO:0001945,postencephalitic Parkinson disease,
+BMGC_DS01928,BMG_DS002470,,Secondary Parkinson Disease,"Parkinson Disease, Secondary",,,,DOID:13548,secondary Parkinson disease,C0030569,D010302,,MONDO:0006966,secondary Parkinson disease,
+BMGC_DS01929,BMG_DS002471,71906005,Paronychia (disorder),,,,,DOID:13117,paronychia,C0030578,,,MONDO:0005898,paronychia,Paronychia | Perionychia | Paronychia (disorder)
+BMGC_DS01930,BMG_DS002472,,Parotid Diseases,Parotid Diseases,,,,DOID:10302,parotid disease,C0030579,D010305,,MONDO:0005899,parotid disorder,
+BMGC_DS01931,BMG_DS002474,196481002;14756005,Parotitis,Parotitis,DA04.2,Sialoadenitis,K11.2,DOID:10301,parotitis,C0030583,D010309,MTHU078653,MONDO:0005900,parotitis,Sialoadenitis (& [parotitis]) | Parotitis | Sialoadenitis | Sialoadenitis (& [parotitis]) (disorder) | Parotitis | Parotitis (disorder)
+BMGC_DS01932,BMG_DS002475,,Parovarian Cyst,Parovarian Cyst,,,,DOID:4333,parovarian cyst,C0030584,D010310,,MONDO:0002965,parovarian cyst,
+BMGC_DS01933,BMG_DS002476,195069001;266305002;155363003,Paroxysmal atrial tachycardia,,,,,,,C0030587,,,,,Atrial paroxysmal tachycardia | Paroxysmal atrial tachycardia | Paroxysmal atrial tachycardia (disorder) | PAT - paroxysmal atrial tachycardia | Supraventricular tachycardia | Parox. supravent. tachycardia | Tachycardia - parox.sup | Paroxysmal atrial tachycardia | Supravent. tach. parox. | Paroxysmal artrial tachycardia | Paroxysmal sup. tachy. | Supraventricular tachycardia (& [paroxysmal] or [paroxysmal artrial]) | Supraventricular tachycardia (& [paroxysmal] or [paroxysmal artrial]) (disorder) | Supraventricular tachycardia (& [paroxysmal] or [paroxysmal artrial]) | Tachycardia - parox.sup | Paroxysmal artrial tachycardia | Paroxysmal sup. tachy. | Paroxysmal atrial tachycardia | Supravent. tach. parox. | Supraventricular tachycardia | Parox. supravent. tachycardia | Supraventricular tachycardia (& [paroxysmal] or [paroxysmal artrial]) (disorder)
+BMGC_DS01934,BMG_DS002477,67198005,Paroxysmal supraventricular tachycardia,,,,,,,C0030590,,MTHU060833,,,Paroxysmal supraventricular tachycardia | Paroxysmal supraventricular tachycardia (disorder)
+BMGC_DS01935,BMG_DS002479,,Pars Planitis,Pars Planitis,,,,DOID:12731,pars planitis,C0030593,D015868,606177,MONDO:0011644,pars planitis,
+BMGC_DS01936,BMG_DS002481,,"Passive Addiction, Neonatal",Neonatal Abstinence Syndrome,,,,,,C0030623,D009357,,,,
+BMGC_DS01937,BMG_DS002482,,Pasteurella Infections,Pasteurella Infections,,,,DOID:11055,pasteurellosis,C0030636,D010326,,MONDO:0005901,pasteurellosis,
+BMGC_DS01938,BMG_DS002483,,,,,,,DOID:12399,pathological gambling,C0030662,,606349,MONDO:0011662,pathological gambling,
+BMGC_DS01939,BMG_DS002484,,Lice Infestations,Lice Infestations,,,,DOID:5502,lice infestation,C0030756,D010373,,MONDO:0003472,lice infestation,
+BMGC_DS01940,BMG_DS002485,81000006,Pediculus capitis infestation,,,,,DOID:5501,Pediculus humanus capitis infestation,C0030757,,,MONDO:0003471,Pediculus humanus capitis infestation,Pediculosis capitis | Head lice infestation | Lousy hair | Nits | Pediculus capitis infestation | Lice infested hair | Nit infested hair | Head louse infestation | Head lice | Pediculosis capitis (disorder)
+BMGC_DS01941,BMG_DS002486,25188002,Body louse infestation,,,,,DOID:5513,Pediculus humanus corporis infestation,C0030758,,,MONDO:0003482,Pediculus humanus corporis infestation,Pediculosis corporis | Body lice | Pediculus corporis infestation | Body louse infestation | Pediculus humanus infestation | Pediculosis corporis (disorder)
+BMGC_DS01942,BMG_DS002487,71011005,Infestation by Phthirus pubis,,1G03,Pthiriasis,B85.3,DOID:13760,Pthirus pubis infestation,C0030759,,,MONDO:0001794,Pthirus pubis infestation,Infestation by Phthirus pubis | Pediculosis pubis | Infestation by crab lice | Crabs | Pubic louse infestation | Pubic lice | Crabs infestation | Phthiriasis pubis | Infestation caused by Phthirus pubis | Infestation caused by Phthirus pubis (disorder) | Infestation caused by crab lice
+BMGC_DS01943,BMG_DS002489,,Pelger-Huet Anomaly,Pelger-Huet Anomaly,,,,DOID:9631,Pelger-Huet anomaly,C0030779,D010381,169400,MONDO:0008214,Pelger-Huet anomaly,
+BMGC_DS01944,BMG_DS002490,,Peliosis Hepatis,Peliosis Hepatis,,,,DOID:914,peliosis hepatis,C0030781,D010382,,MONDO:0004717,peliosis hepatis,
+BMGC_DS01945,BMG_DS002491,267491008;154725000;418186002,Pellagra,Pellagra,,,,DOID:8457,pellagra,C0030783,D010383,,MONDO:0019975,pellagra,Vitamin deficiency: [thiamine/niacin] or [beriberi] or [pellagra] or [thiamine] | Pellagra | Thiamine/niacin deficiency | Beriberi | Beri-beri | Thiamine deficiency | Vitamin deficiency: [thiamine/niacin] or [beriberi] or [pellagra] or [thiamine] (disorder) | Vitamin deficiency: [thiamine/niacin] or [beriberi] or [pellagra] or [thiamine] | Beriberi | Thiamine/niacin deficiency | Beri-beri | Thiamine deficiency | Pellagra | Vitamin deficiency: [thiamine/niacin] or [beriberi] or [pellagra] or [thiamine] (disorder) | Pellagra (disorder) | Pellagra
+BMGC_DS01946,BMG_DS002492,111367007,Pelvic abscess,,,,,,,C0030785,,,,,Pelvic abscess | Pelvic abscess (disorder)
+BMGC_DS01947,BMG_DS002493,,Pelvic Infection,Pelvic Infection,,,,,,C0030790,D034161,,,,
+BMGC_DS01948,BMG_DS002494,,"Pemphigoid, Benign Mucous Membrane","Pemphigoid, Benign Mucous Membrane",,,,DOID:11656,cicatricial pemphigoid,C0030804,D010390,,MONDO:0018746,mucous membrane pemphigoid,
+BMGC_DS01949,BMG_DS002495,77090002,Bullous pemphigoid,,EB41.0,Bullous pemphigoid,L12.0,DOID:8506,bullous pemphigoid,C0030805,,MTHU055608,MONDO:0019082,bullous pemphigoid,Bullous pemphigoid | Bullous pemphigoid (disorder) | BP - Bullous pemphigoid
+BMGC_DS01950,BMG_DS002496,156355008;65172003,Pemphigus,Pemphigus,,,L10,DOID:9182,pemphigus,C0030807,D010392,,MONDO:0006594,pemphigus,Pemphigus | Pemphigus (disorder)
+BMGC_DS01951,BMG_DS002497,,Pemphigus Vulgaris,Pemphigus,,,,DOID:0060851,pemphigus vulgaris,C0030809,D010392,169610,MONDO:0008219,pemphigus vulgaris,
+BMGC_DS01952,BMG_DS002499,,Penile Diseases,Penile Diseases,,,,,,C0030846,D010409,,MONDO:0002036,penile disorder,
+BMGC_DS01953,BMG_DS002500,,Peyronie Disease,Penile Induration,,,,DOID:8616,Peyronie's disease,C0030848,D010411,171000,MONDO:0008231,Peyronie disease,
+BMGC_DS01954,BMG_DS002501,,,,,,,DOID:11624,penile benign neoplasm,C0030849,,,MONDO:0006895,penile neoplasm,
+BMGC_DS01955,BMG_DS002502,,Peptic Ulcer,Peptic Ulcer,,,,DOID:750,peptic ulcer disease,C0030920,D010437,,MONDO:0004247,peptic ulcer disease,
+BMGC_DS01956,BMG_DS002503,,Peptic Ulcer Perforation,Peptic Ulcer Perforation,,,,DOID:752,peptic ulcer perforation,C0030925,D010439,,MONDO:0004260,peptic ulcer perforation,
+BMGC_DS01957,BMG_DS002506,,Suppurative Periapical Periodontitis,Periapical Abscess,,,,DOID:2562,suppurative periapical periodontitis,C0031024,D010482,,MONDO:0006989,suppurative periapical periodontitis,
+BMGC_DS01958,BMG_DS002508,,Periapical Granuloma,Periapical Granuloma,,,,DOID:4617,periapical granuloma,C0031029,D010484,,MONDO:0006897,periapical granuloma,
+BMGC_DS01959,BMG_DS002509,,Periapical Periodontitis,Periapical Periodontitis,,,,DOID:823,periapical periodontitis,C0031030,D010485,,MONDO:0004508,periapical periodontitis,
+BMGC_DS01960,BMG_DS002512,,Polyarteritis Nodosa,Polyarteritis Nodosa,,,,DOID:9810,polyarteritis nodosa,C0031036,D010488,,MONDO:0019170,polyarteritis nodosa,
+BMGC_DS01961,BMG_DS002513,50921008,Periarthritis,Periarthritis,,,,DOID:2964,periarthritis,C0031037,D010489,,MONDO:0006898,periarthritis,Periarthritis | Periarthritis (disorder)
+BMGC_DS01962,BMG_DS002514,373945007;70370001,Pericardial effusion,,,,,DOID:118,pericardial effusion,C0031039,,MTHU005040,MONDO:0001370,pericardial effusion,Pericardial effusion (disorder) | Pericardial effusion | Hydropericardium | Pericardial effusion | Pericardial effusion (disorder)
+BMGC_DS01963,BMG_DS002515,3238004,Pericarditis,Pericarditis,,,,DOID:1787,pericarditis,C0031046,D010493,MTHU011706,MONDO:0005904,pericarditis,Pericarditis | Pericarditis (disorder)
+BMGC_DS01964,BMG_DS002516,,"Pericarditis, Constrictive","Pericarditis, Constrictive",,,,DOID:11481,constrictive pericarditis,C0031048,D010494,,MONDO:0006711,constrictive pericarditis,
+BMGC_DS01965,BMG_DS002518,,Pericementitis,Periodontitis,,,,,,C0031051,D010518,,,,
+BMGC_DS01966,BMG_DS002519,111373008,Pericholangitis,,,,,DOID:14272,pericholangitis,C0031052,,,MONDO:0001931,pericholangitis,Pericholangitis | Pericholangitis (disorder)
+BMGC_DS01967,BMG_DS002521,22240003,Pericoronitis,Pericoronitis,,,,DOID:3671,pericoronitis,C0031055,D010497,,MONDO:0006899,pericoronitis,Pericoronitis | Pericoronitis (disorder)
+BMGC_DS01968,BMG_DS002522,111404004,Perinephritis,Perinephritis,,,,DOID:2982,perinephritis,C0031065,D010501,,MONDO:0006900,perinephritis,Perinephritis | Perinephritis (disorder)
+BMGC_DS01969,BMG_DS002523,,Familial Mediterranean Fever,Familial Mediterranean Fever,,,,DOID:2987,familial Mediterranean fever,C0031069,D010505,,MONDO:0018088,familial Mediterranean fever,
+BMGC_DS01970,BMG_DS002525,,Periodontal Diseases,Periodontal Diseases,,,,DOID:3388,periodontal disease,C0031090,D010510,,MONDO:0002635,periodontal disorder,
+BMGC_DS01971,BMG_DS002526,155648008;266491004;41565005,Periodontitis,Periodontitis,,,,DOID:824,periodontitis,C0031099,D010518,MTHU009733,MONDO:0005076,periodontitis,(Gingival and periodontal disease NOS) or (giant cell epulis) or (periodontitis) | Gingival/periodontal dis. NOS | Gingival and periodontal disease NOS | Giant cell epulis | Periodontitis | (Gingival and periodontal disease NOS) or (giant cell epulis) or (periodontitis) (disorder) | Periodontitis | Giant cell epulis | Gingival/periodontal dis. NOS | Gingival and periodontal disease NOS | (Gingival and periodontal disease NOS) or (giant cell epulis) or (periodontitis) | (Gingival and periodontal disease NOS) or (giant cell epulis) or (periodontitis) (disorder) | Periodontitis | Periodontitis (disorder)
+BMGC_DS01972,BMG_DS002527,,Aggressive Periodontitis,Aggressive Periodontitis,,,,DOID:1474,aggressive periodontitis,C0031106,D010520,,,,
+BMGC_DS01973,BMG_DS002528,41910004,Periostitis,Periostitis,,,,DOID:9957,periostitis,C0031111,D010522,,MONDO:0004934,periostitis,Periostitis | Periosteitis fibrosa | Periostitis (disorder)
+BMGC_DS01974,BMG_DS002529,,,,,,,DOID:341,peripheral vascular disease,C0031115,,,,,
+BMGC_DS01975,BMG_DS002530,,,,,,,DOID:574,peripheral nervous system disease,C0031117,,,MONDO:0005244,peripheral neuropathy,
+BMGC_DS01976,BMG_DS002531,,,,,,,DOID:1192,peripheral nervous system neoplasm,C0031118,,,MONDO:0001406,peripheral nervous system neoplasm,
+BMGC_DS01977,BMG_DS002534,36675003,Periphlebitis,Phlebitis,,,,,,C0031129,D010689,,,,Periphlebitis | Periphlebitis (disorder)
+BMGC_DS01978,BMG_DS002537,,,,,,,,,C0031149,,,MONDO:0006901,peritoneal neoplasm,
+BMGC_DS01979,BMG_DS002538,,,,,,,,,C0031154,,,MONDO:0004522,peritonitis,
+BMGC_DS01980,BMG_DS002539,,Peritonsillar Abscess,Peritonsillar Abscess,,,,,,C0031157,D000039,,MONDO:0005906,peritonsillar abscess,
+BMGC_DS01981,BMG_DS002542,,Persistent Fetal Circulation Syndrome,Persistent Fetal Circulation Syndrome,,,,DOID:13042,persistent fetal circulation syndrome,C0031190,D010547,,MONDO:0022430,persistent fetal circulation syndrome,
+BMGC_DS01982,BMG_DS002545,,Peutz-Jeghers Syndrome,Peutz-Jeghers Syndrome,,,,DOID:3852,Peutz-Jeghers syndrome,C0031269,D010580,175200,MONDO:0008280,Peutz-Jeghers syndrome,
+BMGC_DS01983,BMG_DS002546,,Phagocyte Bactericidal Dysfunction,Phagocyte Bactericidal Dysfunction,,,,DOID:3262,phagocyte bactericidal dysfunction,C0031306,D010585,,MONDO:0005910,phagocyte bactericidal dysfunction,
+BMGC_DS01984,BMG_DS002547,,Pharyngeal Diseases,Pharyngeal Diseases,,,,DOID:2275,pharyngitis,C0031345,D010608,,MONDO:0020592,disorder of pharynx,
+BMGC_DS01985,BMG_DS002548,,,,,,,DOID:0060119,pharynx cancer,C0031347,,,MONDO:0021246,pharynx neoplasm,
+BMGC_DS01986,BMG_DS002549,37616004;405737000,Pharyngitis,Pharyngitis,,,,DOID:2275,pharyngitis,C0031350,D010612,MTHU007438,MONDO:0002258,pharyngitis,Pharyngitis | Sore throat | Irritation of the throat | Pharyngeal pain | Throat infection | Throat infection - pharyngitis | Throat soreness | Pharyngitis (disorder) | Pharyngitis (disorder) | Pharyngitis
+BMGC_DS01987,BMG_DS002550,,Pharyngo-Conjunctival Fever,"Adenovirus Infections, Human",,,,DOID:13801,pharyngoconjunctival fever,C0031351,D000258,,MONDO:0005911,pharyngoconjunctival fever,
+BMGC_DS01988,BMG_DS002551,,,,,,,DOID:5062,phencyclidine abuse,C0031391,,,MONDO:0005912,phencyclidine abuse,
+BMGC_DS01989,BMG_DS002552,,Phenylketonurias,Phenylketonurias,,,,DOID:9281,phenylketonuria,C0031485,D010661,261600,MONDO:0009861,phenylketonuria,
+BMGC_DS01990,BMG_DS002553,,,,,,,,,C0031511,,171300,MONDO:0008233,pheochromocytoma,
+BMGC_DS01991,BMG_DS002554,,,,,,,DOID:2712,phimosis,C0031538,,,,,
+BMGC_DS01992,BMG_DS002555,,,,,,,DOID:864,phlebitis,C0031542,,,MONDO:0004625,phlebitis,
+BMGC_DS01993,BMG_DS002556,,Phlegmasia Alba Dolens,Thrombophlebitis,,,,,,C0031556,D013924,,,,
+BMGC_DS01994,BMG_DS002557,,,,,,,DOID:11257,social phobia,C0031572,,,MONDO:0001247,social phobia,
+BMGC_DS01995,BMG_DS002558,,Phosphorus Metabolism Disorders,Phosphorus Metabolism Disorders,,,,DOID:2485,phosphorus metabolism disease,C0031707,D010760,,MONDO:0002319,phosphorus metabolism disease,
+BMGC_DS01996,BMG_DS002559,61064008;367484009;238525001,Polymorphous light eruption,,EJ30.0,Polymorphic light eruption,L56.4,,,C0031736,,,MONDO:0041182,polymorphic light eruption,Polymorphous light eruption | Polymorphous light eruption (disorder) | Photodermatitis due to sun | Polymorphous light eruption (disorder) | Polymorphous light eruption | Polymorphic light eruption | Polymorphous light eruption | Polymorphic photodermatitis | Polymorphic light eruption (disorder) | Pruritus estivalis | Pruritus aestivalis | PLE - polymorphic light eruption
+BMGC_DS01997,BMG_DS002560,,Photosensitivity Disorders,Photosensitivity Disorders,,,,DOID:3159,photosensitivity disease,C0031762,D010787,,MONDO:0006597,photosensitivity disease,
+BMGC_DS01998,BMG_DS002562,,,,,,,DOID:12128,pica disease,C0031873,,,MONDO:0001441,pica disease,
+BMGC_DS01999,BMG_DS002563,,Pick Disease of Heart,"Pericarditis, Constrictive",,,,,,C0031876,D010494,,,,
+BMGC_DS02000,BMG_DS002564,,Obesity Hypoventilation Syndrome,Obesity Hypoventilation Syndrome,,,,,,C0031880,D010845,257500,MONDO:0009763,obesity-hypoventilation syndrome,
+BMGC_DS02001,BMG_DS002566,402135006;266218008;154408001,Piedra,Piedra,,,,DOID:13902;DOID:0050133;DOID:12711,white piedra | superficial mycosis | black piedra,C0031898,D010854,,MONDO:0000253,piedra,Piedra (disorder) | Piedra | Coccidioidomycosis | Other mycoses | Sporotrichosis | Mycoses - other | Piedra | Histoplasmosis | Aspergillosis | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) (disorder) | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) | Aspergillosis | Mycoses - other | Histoplasmosis | Other mycoses | Piedra | Sporotrichosis | Coccidioidomycosis | Other mycoses (& [aspergillosis] or [coccidioidomycosis] or [histoplasmosis] or [piedra] or [sporotrichosis]) (disorder)
+BMGC_DS02002,BMG_DS002567,,,,,,,DOID:4258,Weissenbacher-Zweymuller syndrome,C0031900,,261800,MONDO:0009869,isolated Pierre-Robin syndrome,
+BMGC_DS02003,BMG_DS002569,,,,,,,,,C0031925,,173000,MONDO:0008249,pilonidal sinus,
+BMGC_DS02004,BMG_DS002570,,,,,,,DOID:5032,pineal gland cancer,C0031941,,,,,
+BMGC_DS02005,BMG_DS002571,22064009,Pinta,Pinta,,,,DOID:1022,pinta disease,C0031946,D010874,,MONDO:0000979,pinta disease,Pinta | Azul | Infection by Treponema carateum | Carate | Pinta (disorder) | Mal del pinto
+BMGC_DS02006,BMG_DS002572,,,,,,,DOID:3829,pituitary adenoma,C0032000,,,MONDO:0006373,pituitary gland adenoma,
+BMGC_DS02007,BMG_DS002573,,Pituitary Apoplexy,Pituitary Apoplexy,,,,DOID:1129,pituitary apoplexy,C0032001,D010899,,MONDO:0006908,pituitary apoplexy,
+BMGC_DS02008,BMG_DS002574,,Pituitary Diseases,Pituitary Diseases,,,,,,C0032002,D010900,,MONDO:0003381,pituitary gland disorder,
+BMGC_DS02009,BMG_DS002575,,,,,,,DOID:1785,pituitary cancer,C0032019,,,MONDO:0017611,pituitary tumor,
+BMGC_DS02010,BMG_DS002576,34630004;274133009;156372001,Pityriasis,Pityriasis,,,,,,C0032024,D010915,,MONDO:0024248,obsolete pityriasis,Pityriasis | Pityriasis (disorder)
+BMGC_DS02011,BMG_DS002577,,Pityriasis Rosea,Pityriasis Rosea,,,,DOID:8892,pityriasis rosea,C0032026,D017515,,MONDO:0006601,pityriasis rosea,
+BMGC_DS02012,BMG_DS002578,,Pityriasis Rubra Pilaris,Pityriasis Rubra Pilaris,,,,DOID:9212,pityriasis rubra pilaris,C0032027,D010916,,MONDO:0100017,pityriasis rubra pilaris,
+BMGC_DS02013,BMG_DS002579,,,,,,,DOID:4744,placenta accreta,C0032044,,,MONDO:0005916,placenta accreta,
+BMGC_DS02014,BMG_DS002580,,,,,,,DOID:780,placenta disease,C0032045,,,MONDO:0005917,placenta disorder,
+BMGC_DS02015,BMG_DS002581,,,,,,,DOID:11060,placenta praevia,C0032046,,,MONDO:0005918,placenta praevia,
+BMGC_DS02016,BMG_DS002582,,Placental Insufficiency,Placental Insufficiency,,,,DOID:3891,placental insufficiency,C0032051,D010927,,MONDO:0005919,placental insufficiency,
+BMGC_DS02017,BMG_DS002584,58750007,Plague,Plague,,,A20,DOID:3482,plague,C0032064,D010930,,MONDO:0019095,plague,Plague | Infection by Yersinia pestis | Pest | Pestilential fever | Black death | Plague (disorder)
+BMGC_DS02018,BMG_DS002587,,,,,,,DOID:3721,plasmacytoma,C0032131,,,MONDO:0005615,plasmacytoma,
+BMGC_DS02019,BMG_DS002588,,Platelet Storage Pool Deficiency,Platelet Storage Pool Deficiency,,,,DOID:2223,platelet storage pool deficiency,C0032197,D010981,185050,MONDO:0008495,platelet storage pool deficiency,
+BMGC_DS02020,BMG_DS002589,,Pleural Diseases,Pleural Diseases,,,,DOID:1532,pleural disease,C0032226,D010995,,MONDO:0002037,pleural disorder,
+BMGC_DS02021,BMG_DS002590,,,,,,,DOID:5158,pleural cancer,C0032229,,,MONDO:0021065,pleural neoplasm,
+BMGC_DS02022,BMG_DS002591,196075003;266406002;32203001,Pleurisy,Pleurisy,MD31,Pleurisy,R09.1,,,C0032231,D010998,MTHU075704,MONDO:0000986,pleurisy,Pleurisy | Pleuritis | Pleurisy (disorder) | (Pleurisy) or (adhesions - pleural) | Pleurisy | Adhesions - pleural | (Pleurisy) or (adhesions - pleural) (disorder) | Pleurisy | Pleurisy (disorder)
+BMGC_DS02023,BMG_DS002592,,"Pleurodynia, Epidemic","Pleurodynia, Epidemic",,,,DOID:10882,epidemic pleurodynia,C0032238,D011000,,MONDO:0005751,epidemic pleurodynia,
+BMGC_DS02024,BMG_DS002593,60485005,Pleuropneumonia,Pleuropneumonia,,,,DOID:14319,pleuropneumonia,C0032241,D011001,,MONDO:0001940,pleuropneumonia,Pleurobronchopneumonia | Pleuropneumonia | Pleurobronchopneumonia (disorder)
+BMGC_DS02025,BMG_DS002596,,Pneumatosis Cystoides Intestinalis,Pneumatosis Cystoides Intestinalis,,,,DOID:13249,pneumatosis cystoides intestinalis,C0032266,D011006,,MONDO:0006912,pneumatosis cystoides intestinalis,
+BMGC_DS02026,BMG_DS002598,,Pneumococcal Infections,Pneumococcal Infections,,,,,,C0032269,D011008,,MONDO:0005114,pneumococcal infection,
+BMGC_DS02027,BMG_DS002599,155587002;40122008;196004000,Pneumoconiosis,Pneumoconiosis,,,,DOID:10316,pneumoconiosis,C0032273,D011009,,MONDO:0015926,pneumoconiosis,Pneumoconiosis | Pneumoconiosis (disorder) | Pneumoconiosis | Pneumoconiosis (disorder) | PK - Pneumoconiosis | Lung disease: [pneumoconioses] or [occupational] or [due to external agents] | Lung disease due to external agents | Pneumoconiosis | Occupational lung disease | Pneumoconioses | Lung disease: [pneumoconioses] or [occupational] or [due to external agents] (disorder)
+BMGC_DS02028,BMG_DS002601,60363000;155548002;266391003;233604007,Pneumonia,Pneumonia,,,,DOID:552,pneumonia,C0032285,D011014,MTHU002638,MONDO:0005249,pneumonia,Pneumonia | Pneumonia (disorder) | Pneumonia and influenza &/or pneumonia | Pneumonia | Pneumonia and influenza | Pneumonia and influenza &/or pneumonia (disorder)
+BMGC_DS02029,BMG_DS002603,,Aspiration Pneumonia,"Pneumonia, Aspiration",,,,DOID:0050152;DOID:3240,aspiration pneumonitis | aspiration pneumonia,C0032290,D011015,,MONDO:0000265,aspiration pneumonia,
+BMGC_DS02030,BMG_DS002605,,"Pneumonia, Lipid","Pneumonia, Lipid",,,,DOID:3241,lipid pneumonia,C0032298,D011017,,MONDO:0005826,lipid pneumonia,
+BMGC_DS02031,BMG_DS002606,,Lobar Pneumonia,Pneumonia,,,,,,C0032300,D011014,,,,
+BMGC_DS02032,BMG_DS002607,46970008,Mycoplasma pneumonia,,,,,,,C0032302,,,MONDO:0005867,Mycoplasma pneumoniae pneumonia,Mycoplasma pneumonia | Endemic pneumonia | Mycoplasma pneumoniae pneumonia | Mycoplasmal pneumonia | Eaton's agent pneumonia | Pneumonia caused by Mycoplasma pneumoniae | Primary atypical pneumonia caused by Mycoplasma pneumoniae | Pneumonia caused by Mycoplasma pneumoniae (disorder)
+BMGC_DS02033,BMG_DS002610,,Staphylococcal Pneumonia,"Pneumonia, Staphylococcal",,,,,,C0032308,D011023,,MONDO:0005970,staphylococcal pneumonia,
+BMGC_DS02034,BMG_DS002611,,"Pneumonia, Viral","Pneumonia, Viral",,,,DOID:10533,viral pneumonia,C0032310,D011024,,MONDO:0006012,viral pneumonia,
+BMGC_DS02035,BMG_DS002612,389994007;390745009;82542004,Pneumopericardium,Pneumopericardium,,,,,,C0032319,D011026,,,,Pneumopericardium | Pneumopericardium (disorder)
+BMGC_DS02036,BMG_DS002614,36118008;155609008,Pneumothorax,Pneumothorax,,,,,,C0032326,D011030,MTHU016219,MONDO:0002076,pneumothorax,Pneumothorax | Pneumothorax (disorder)
+BMGC_DS02037,BMG_DS002615,205572001;205565002;69093006,Rothmund-Thomson syndrome,,,,,DOID:2732,Rothmund-Thomson syndrome,C0032339,,,MONDO:0010002,Rothmund-Thomson syndrome,Rothmund-Thomson syndrome | Rothmund-Thomson syndrome (disorder) | Rothmund-Thomson syndrome | Poikiloderma congenitale syndrome | Rothmund-Thomson syndrome (disorder) | Poikiloderma congenitale
+BMGC_DS02038,BMG_DS002616,,"Dermatitis, Toxicodendron","Dermatitis, Toxicodendron",,,,DOID:3819,toxicodendron dermatitis,C0032342,D011040,,MONDO:0006616,toxicodendron dermatitis,
+BMGC_DS02039,BMG_DS002617,,Poland Syndrome,Poland Syndrome,,,,DOID:12961,Poland syndrome,C0032357,D011045,173800,MONDO:0008262,Poland syndrome,
+BMGC_DS02040,BMG_DS002618,398102009;367318001;186475007;54839009,Poliomyelitis,Poliomyelitis,,,,DOID:4953,poliomyelitis,C0032371,D011051,,MONDO:0017373,poliomyelitis,Acute poliomyelitis (disorder) | Acute poliomyelitis | Polio | PM - Poliomyelitis | Poliomyelitis | Poliomyelitis | Poliomyelitis (disorder) | Acute poliomyelitis | Infantile paralysis | Poliomyelitis | Epidemic acute poliomyelitis | PM - Poliomyelitis | Polio | Anterior acute poliomyelitis | Acute poliomyelitis (disorder) | Acute poliomyelitis | Epidemic acute poliomyelitis | Poliomyelitis | Infantile paralysis | Anterior acute poliomyelitis | PM - Poliomyelitis | Polio | Acute poliomyelitis (disorder)
+BMGC_DS02041,BMG_DS002620,,"Polychondritis, Relapsing","Polychondritis, Relapsing",,,,DOID:2556,relapsing polychondritis,C0032453,D011081,,MONDO:0019125,relapsing polychondritis,
+BMGC_DS02042,BMG_DS002621,,Polycystic Ovary Syndrome,Polycystic Ovary Syndrome,,,,DOID:11612,polycystic ovary syndrome,C0032460,D011085,184700,MONDO:0008487,polycystic ovary syndrome,
+BMGC_DS02043,BMG_DS002622,127062003,Polycythemia,Polycythemia,,,,DOID:8432,polycythemia,C0032461,D011086,MTHU006480,MONDO:0005571,polycythemia,Erythrocytosis | Polycythemia | Polycythaemia | Erythrocytosis (disorder)
+BMGC_DS02044,BMG_DS002623,,,,,,,DOID:8997,polycythemia vera,C0032463,,263300,MONDO:0009891,acquired polycythemia vera,
+BMGC_DS02045,BMG_DS002624,52754008;156043009;266671004,Polymenorrhea,Menstruation Disturbances,GA20.Z,"Menstrual cycle bleeding disorders, unspecified",N92.0,,,C0032519,D008599,,,,Polymenorrhea | Unusually frequent menses | Polymenorrhoea | Epimenorrhoea | Epimenorrhea | Polymenorrhea (finding) | Abnormally frequent menstruation | Frequent periods | (Polymenorrhea) or (epimenorrhea) or (frequent periods) | (Polymenorrhoea) or (epimenorrhoea) or (frequent periods) | Epimenorrhea | Polymenorrhea | Polymenorrhoea | Epimenorrhoea | (Polymenorrhoea) or (epimenorrhoea) or (frequent periods) (finding) | (Polymenorrhea) or (epimenorrhea) or (frequent periods) | Frequent periods | Epimenorrhoea | Polymenorrhoea | (Polymenorrhoea) or (epimenorrhoea) or (frequent periods) | Epimenorrhea | Polymenorrhea | (Polymenorrhoea) or (epimenorrhoea) or (frequent periods) (disorder)
+BMGC_DS02046,BMG_DS002625,,Polymyalgia Rheumatica,Polymyalgia Rheumatica,,,,DOID:853,polymyalgia rheumatica,C0032533,D011111,,MONDO:0019735,polymyalgia rheumatica,
+BMGC_DS02047,BMG_DS002626,300951006;76886005,Polyneuritis,Neuritis,,,,,,C0032541,D009443,MTHU068156,MONDO:0021718,polyneuritis,Polyneuritis | Polyneuritis (disorder) | Polyneuritis | Polyneuritis (disorder) | Inflammatory polyneuropathy
+BMGC_DS02048,BMG_DS002628,,,,,,,,,C0032578,,,MONDO:0019934,polyploidy,
+BMGC_DS02049,BMG_DS002629,,,,,,,DOID:0050424,familial adenomatous polyposis,C0032580,,,MONDO:0021055,classic familial adenomatous polyposis,
+BMGC_DS02050,BMG_DS002630,,,,,,,,,C0032584,,,MONDO:0005079,polyp,
+BMGC_DS02051,BMG_DS002631,75572007,Polyradiculopathy,Polyradiculopathy,,,,DOID:4307,polyradiculopathy,C0032586,D011128,,MONDO:0002960,polyradiculopathy,Polyradiculopathy | Polyradiculopathy (disorder)
+BMGC_DS02052,BMG_DS002632,128078004,Polyradiculoneuropathy,Polyradiculoneuropathy,,,,DOID:4308,polyradiculoneuropathy,C0032587,D011129,,MONDO:0006915,polyradiculoneuropathy,Polyradiculoneuropathy | Polyradiculoneuropathy (disorder)
+BMGC_DS02053,BMG_DS002633,402567004,Vesicular eczema of hands and/or feet,,,,,DOID:9230,pompholyx,C0032633,,,MONDO:0006540,dyshidrosis,Vesicular eczema of hands and/or feet (disorder) | Vesicular eczema of hands and/or feet | Cheiropodopompholyx | Pompholyx | Pompholyx eczema | Vesicular eczema of hands and feet | Dyshidrotic dermatitis | Dyshidrotic eczema | Dyshidria
+BMGC_DS02054,BMG_DS002634,,,,,,,,,C0032650,,175750,MONDO:0008288,popliteal cyst,
+BMGC_DS02055,BMG_DS002636,,,,,,,DOID:13268,porphyria,C0032708,,,MONDO:0037821,porphyrin metabolism disease,
+BMGC_DS02056,BMG_DS002639,,Postgastrectomy Syndromes,Postgastrectomy Syndromes,,,,DOID:8439,postgastrectomy syndrome,C0032763,D011178,,MONDO:0004566,postgastrectomy syndrome,
+BMGC_DS02057,BMG_DS002640,2177002;186516001,Postherpetic neuralgia,,,,,,,C0032768,,,MONDO:0041052,postherpetic neuralgia,Postherpetic neuralgia | Postherpetic neuralgia (disorder) | PHN - Post-herpetic neuralgia | Post-zoster neuralgia | (Herpes zoster with other CNS complication) or (postherpetic neuralgia) | Herpes zoster with other central nervous system complication | (Herpes zoster with other CNS complication) or (postherpetic neuralgia) (disorder)
+BMGC_DS02058,BMG_DS002643,,Postphlebitic Syndrome,Postphlebitic Syndrome,,,,DOID:2364,post-thrombotic syndrome,C0032807,D011186,,MONDO:0005928,post-thrombotic syndrome,
+BMGC_DS02059,BMG_DS002649,205794007,Prader-Willi Syndrome,Prader-Willi Syndrome,,,,DOID:11983,Prader-Willi syndrome,C0032897,D011218,176270,MONDO:0008300,Prader-Willi syndrome,(Multiple system congenital anomalies NEC) or (Prader-Willi syndrome) or (Noonan's syndrome) | Prader-Willi Syndrome | Prader-Willi syndrome | Prader - Willi syndrome | Multiple system congenital anomalies NEC | Noonan's syndrome | (Multiple system congenital anomalies NEC) or (Prader-Willi syndrome) or (Noonan's syndrome) (disorder)
+BMGC_DS02060,BMG_DS002650,,,,,,,DOID:10591,pre-eclampsia,C0032914,,,MONDO:0005081,preeclampsia,
+BMGC_DS02061,BMG_DS002654,,,,,,,DOID:780,placenta disease,C0032962,,,,,
+BMGC_DS02062,BMG_DS002655,,"Pregnancy Complications, Cardiovascular","Pregnancy Complications, Cardiovascular",,,,,,C0032963,D011249,,,,
+BMGC_DS02063,BMG_DS002656,,"Pregnancy Complications, Hematologic","Pregnancy Complications, Hematologic",,,,,,C0032964,D011250,,,,
+BMGC_DS02064,BMG_DS002657,,"Pregnancy Complications, Infectious","Pregnancy Complications, Infectious",,,,,,C0032965,D011251,,,,
+BMGC_DS02065,BMG_DS002660,,,,,,,DOID:0060329,ectopic pregnancy,C0032987,,,MONDO:0000755,ectopic pregnancy,
+BMGC_DS02066,BMG_DS002663,,Atrial Premature Complexes,Atrial Premature Complexes,,,,,,C0033036,D018880,,,,
+BMGC_DS02067,BMG_DS002664,,,,,,,DOID:13709,premature ejaculation,C0033038,,,MONDO:0001780,premature ejaculation,
+BMGC_DS02068,BMG_DS002667,155135005;41256004,Presbyopia,Presbyopia,9D00.3,Presbyopia,H52.4,DOID:11638,presbyopia,C0033075,D011305,,MONDO:0001330,presbyopia,Presbyopia | Presbyopia (disorder)
+BMGC_DS02069,BMG_DS002669,155930001;6273006;198027001,Priapism,Priapism,GB06.1,Priapism,N48.3,DOID:9286,priapism,C0033117,D011317,MTHU054345,MONDO:0004745,priapism,Priapism | Priapism (disorder) | Priapism | Mentulagra | Pathologic erection | Priapism (disorder) | (Priapism) or (erection - painful) | Priapism | Erection - painful | Painful erection | (Priapism) or (erection - painful) (disorder)
+BMGC_DS02070,BMG_DS002671,,"Cerebellar Degenerations, Primary",Spinocerebellar Degenerations,,,,DOID:9277,primary cerebellar degeneration,C0033132,D013132,,MONDO:0004742,primary cerebellar degeneration,
+BMGC_DS02071,BMG_DS002672,,Primary Insomnia,Sleep Initiation and Maintenance Disorders,,,,,,C0033139,D007319,,,,
+BMGC_DS02072,BMG_DS002673,,"Cardiomyopathies, Primary",Cardiomyopathies,,,,DOID:0050700,cardiomyopathy,C0033141,D009202,,MONDO:0005110,idiopathic cardiomyopathy,
+BMGC_DS02073,BMG_DS002674,3951002;155806004;266534007,Proctitis,Proctitis,,,,DOID:3127,proctitis,C0033246,D011349,MTHU007443,MONDO:0005538,proctitis,Proctitis | Proctitis (disorder) | (GIT disorders NOS) or (kraurosis of anus) or (proctitis) or (rectal irritation) or (stercoral ulcer) | Irritation - rectum | Kraurosis ani | Ulcer - stercoral | Gastrointestinal tract disorders NOS | Anus - kraurosis | GIT disorders NOS | Proctitis | Rectal irritation | Kraurosis of anus | (GIT disorders NOS) or (kraurosis of anus) or (proctitis) or (rectal irritation) or (stercoral ulcer) (disorder) | (GIT disorders NOS) or (kraurosis of anus) or (proctitis) or (rectal irritation) or (stercoral ulcer) | Kraurosis of anus | Kraurosis ani | Proctitis | Ulcer - stercoral | Gastrointestinal tract disorders NOS | GIT disorders NOS | Irritation - rectum | Rectal irritation | Anus - kraurosis | (GIT disorders NOS) or (kraurosis of anus) or (proctitis) or (rectal irritation) or (stercoral ulcer) (disorder)
+BMGC_DS02074,BMG_DS002678,190590004;238869000;238870004,Progeria,Progeria,5B3Z,"Endocrine diseases, unspecified",E34.8,DOID:3911,progeria,C0033300,D011371,176670,MONDO:0008310;MONDO:0020732,Hutchinson-Gilford progeria syndrome | progeria,Premature ageing syndrome | Adult premature ageing syndrome | Progeria syndrome | Adult premature aging syndrome | Premature aging syndrome | Progeria | Progeria (disorder) | Progeria | Progeria (disorder) | Hutchinson-Gilford syndrome | Progeria syndrome | Premature senility syndrome | Hutchinson-Gilford syndrome (disorder) | Progeria
+BMGC_DS02075,BMG_DS002680,,,,,,,DOID:5394,prolactinoma,C0033375,,600634,MONDO:0010911,prolactin-producing pituitary gland adenoma,
+BMGC_DS02076,BMG_DS002682,,Prostatic Diseases,Prostatic Diseases,,,,DOID:47,prostate disease,C0033575,D011469,,MONDO:0003105,prostate disorder,
+BMGC_DS02077,BMG_DS002683,,,,,,,DOID:10283,prostate cancer,C0033578,,,MONDO:0021259,prostate neoplasm,
+BMGC_DS02078,BMG_DS002685,,,,,,,DOID:14654,prostatitis,C0033581,,,MONDO:0005280,prostatitis,
+BMGC_DS02079,BMG_DS002686,,Prosthesis Loosening,Prosthesis Failure,,,,,,C0033587,D011475,,,,
+BMGC_DS02080,BMG_DS002687,,Protein Deficiency,Protein Deficiency,,,,,,C0033626,D011488,,,,
+BMGC_DS02081,BMG_DS002688,,,,,,,DOID:11801,protein-energy malnutrition,C0033677,,,MONDO:0001371,protein-energy malnutrition,
+BMGC_DS02082,BMG_DS002689,,Protein-Losing Enteropathies,Protein-Losing Enteropathies,,,,DOID:10611,protein-losing enteropathy,C0033680,D011504,226300,MONDO:0009174,protein-losing enteropathy,
+BMGC_DS02083,BMG_DS002690,,,,,,,DOID:576,proteinuria,C0033687,,,MONDO:0003634,proteinuria,
+BMGC_DS02084,BMG_DS002691,,Proteus Infections,Proteus Infections,,,,,,C0033700,D011512,,MONDO:0006929,Proteus infectious disease,
+BMGC_DS02085,BMG_DS002693,,Protozoan Infections,Protozoan Infections,,,,DOID:2789,parasitic protozoa infectious disease,C0033740,D011528,,MONDO:0002428,protozoa infectious disease,
+BMGC_DS02086,BMG_DS002695,,Prune Belly Syndrome,Prune Belly Syndrome,,,,DOID:0060889,prune belly syndrome,C0033770,D011535,100100,MONDO:0007032,prune belly syndrome,
+BMGC_DS02087,BMG_DS002698,,Pseudo-Hurler Polydystrophy,Mucolipidoses,,,,,,C0033788,D009081,252600,MONDO:0018931,"mucolipidosis type III, alpha/beta",
+BMGC_DS02088,BMG_DS002699,,Pseudobulbar Palsy,Pseudobulbar Palsy,,,,DOID:12680,pseudobulbar palsy,C0033790,D020828,,MONDO:0006930,pseudobulbar palsy,
+BMGC_DS02089,BMG_DS002701,201624004;268142006;156881000;239834007,Pseudogout,,,,,DOID:1156,chondrocalcinosis,C0033802,,MTHU018950,,,(Crystal: [arthropathies] or [arthritis] or [synovitis]) or (chondrocalcinosis) or (pseudogout) | Crystal arthritis | Chondrocalcinosis | Crystal arthropathies | Crystal synovitis | Pseudogout | (Crystal: [arthropathies] or [arthritis] or [synovitis]) or (chondrocalcinosis) or (pseudogout) (disorder) | (Musculoskeletal NOS: [disease] or [disorder]) or (chondrocalcinosis) or (pseudogout) | Chondrocalcinosis | Pseudogout | Musculoskeletal disease NOS | Musculo-skeletal disorder NOS | (Musculoskeletal NOS: [disease] or [disorder]) or (chondrocalcinosis) or (pseudogout) (disorder) | (Musculoskeletal NOS: [disease] or [disorder]) or (chondrocalcinosis) or (pseudogout) | Musculo-skeletal disorder NOS | Chondrocalcinosis | Musculoskeletal disease NOS | Pseudogout | (Musculoskeletal NOS: [disease] or [disorder]) or (chondrocalcinosis) or (pseudogout) (disorder) | Pyrophosphate arthritis | Pyrophosphate arthritis (disorder)
+BMGC_DS02090,BMG_DS002702,,,,,,,DOID:3765,pseudohermaphroditism,C0033804,,,MONDO:0005518,pseudohermaphroditism,
+BMGC_DS02091,BMG_DS002703,77098009,Pseudohypoaldosteronism,Pseudohypoaldosteronism,,,,DOID:4479,pseudohypoaldosteronism,C0033805,D011546,,MONDO:0018638,pseudohypoaldosteronism,Pseudohypoaldosteronism | Pseudohypoadrenocorticalism | Pseudohypoaldosteronism (disorder)
+BMGC_DS02092,BMG_DS002704,58976002;190867002,Pseudohypoparathyroidism,Pseudohypoparathyroidism,5A50.1,Pseudohypoparathyroidism,E20.1,DOID:4184,pseudohypoparathyroidism,C0033806,D011547,MTHU005113,MONDO:0019992,pseudohypoparathyroidism,Pseudohypoparathyroidism | Constitutional chronic hypocalcemia | Familial pseudohypoparathyroidism | Parathyroid hormone resistant hypoparathyroidism | Constitutional chronic hypocalcaemia | Pseudohypoparathyroidism (disorder) | Pseudopseudohypoparathyroidism | Pseudohypoparathyroidism | (Pseudohypoparathyroidism) or (pseudopseudohypoparathyroidism) | (Pseudohypoparathyroidism) or (pseudopseudohypoparathyroidism) (disorder)
+BMGC_DS02093,BMG_DS002705,,Pseudomonas Infections,Pseudomonas Infections,,,,,,C0033817,D011552,,MONDO:0005141,Pseudomonas infection,
+BMGC_DS02094,BMG_DS002706,,,,,,,DOID:3559,pseudomyxoma peritonei,C0033822,,,MONDO:0017048,pseudomyxoma peritonei,
+BMGC_DS02095,BMG_DS002707,8084001;190867002;237659007,Pseudopseudohypoparathyroidism,Pseudopseudohypoparathyroidism,,,,DOID:4183,pseudopseudohypoparathyroidism,C0033835,D011556,612463,MONDO:0012912,pseudopseudohypoparathyroidism,Normocalcemic pseudohypoparathyroidism | Normocalcaemic pseudohypoparathyroidism | Normocalcemic pseudohypoparathyroidism (disorder) | Pseudopseudohypoparathyroidism | Pseudohypoparathyroidism | (Pseudohypoparathyroidism) or (pseudopseudohypoparathyroidism) | (Pseudohypoparathyroidism) or (pseudopseudohypoparathyroidism) (disorder) | Pseudopseudohypoparathyroidism | Pseudopseudohypoparathyroidism (disorder)
+BMGC_DS02096,BMG_DS002708,,Kimura Disease,Kimura Disease,,,,DOID:7365,Kimura disease,C0033838,D000082242,,MONDO:0018830,Kimura disease,
+BMGC_DS02097,BMG_DS002710,,Pseudotumor Cerebri,Pseudotumor Cerebri,,,,DOID:11459,pseudotumor cerebri,C0033845,D011559,243200,MONDO:0009468,pseudotumor cerebri,
+BMGC_DS02098,BMG_DS002711,,Pseudoxanthoma Elasticum,Pseudoxanthoma Elasticum,,,,DOID:2738,pseudoxanthoma elasticum,C0033847,D011561,,MONDO:0024308,pseudoxanthoma elasticum (inherited or acquired),
+BMGC_DS02099,BMG_DS002712,156369008;9014002,Psoriasis,Psoriasis,,,L40,DOID:8893,psoriasis,C0033860,D011565,MTHU036411,MONDO:0005083,psoriasis,Psoriasis | Psoriasis (disorder)
+BMGC_DS02100,BMG_DS002713,,Tension Headache,Tension-Type Headache,,,,,,C0033893,D018781,,,,
+BMGC_DS02101,BMG_DS002714,,,,,,,DOID:252,alcoholic psychosis,C0033936,,,MONDO:0002330,alcoholic psychosis,
+BMGC_DS02102,BMG_DS002715,,,,,,,DOID:1742,drug psychosis,C0033937,,,MONDO:0006730,drug psychosis,
+BMGC_DS02103,BMG_DS002717,,,,,,,DOID:7518,inhibited female orgasm,C0033948,,,,,
+BMGC_DS02104,BMG_DS002718,,,,,,,DOID:5576,inhibited male orgasm,C0033949,,,MONDO:0003522,male orgasm disorder,
+BMGC_DS02105,BMG_DS002719,,,,,,,DOID:10132,psychosexual disorder,C0033951,,,,,
+BMGC_DS02106,BMG_DS002721,,,,,,,,,C0033975,,,MONDO:0005485,psychotic disorder,
+BMGC_DS02107,BMG_DS002722,,,,,,,DOID:0002116,pterygium,C0033999,,,MONDO:0005085,pterygium,
+BMGC_DS02108,BMG_DS002723,,Precocious Puberty,"Puberty, Precocious",,,,,,C0034013,D011629,,MONDO:0000088,precocious puberty,
+BMGC_DS02109,BMG_DS002724,,Puerperal Disorders,Puerperal Disorders,,,,,,C0034040,D011644,,MONDO:0044013,puerperal disorder,
+BMGC_DS02110,BMG_DS002725,,Puerperal Infection,Puerperal Infection,,,,,,C0034041,D011645,,MONDO:0021742,puerperal infection,
+BMGC_DS02111,BMG_DS002727,,Pulmonary Alveolar Proteinosis,Pulmonary Alveolar Proteinosis,,,,DOID:12120,pulmonary alveolar proteinosis,C0034050,D011649,,,,
+BMGC_DS02112,BMG_DS002728,,,,,,,DOID:11396,pulmonary edema,C0034063,,,MONDO:0006932,pulmonary edema,
+BMGC_DS02113,BMG_DS002729,,,,,,,DOID:9477,pulmonary embolism,C0034065,,,MONDO:0005279,pulmonary embolism,
+BMGC_DS02114,BMG_DS002730,1001000119102,Pulmonary embolism with pulmonary infarction,,,,,DOID:8516,pulmonary embolism and infarction,C0034066,,,,,Pulmonary embolism with pulmonary infarction | Pulmonary embolism with pulmonary infarction (disorder) | Pulmonary embolism with infarction
+BMGC_DS02115,BMG_DS002731,,Pulmonary Emphysema,Pulmonary Emphysema,,,,,,C0034067,D011656,,MONDO:0004849,pulmonary emphysema,
+BMGC_DS02116,BMG_DS002732,,Pulmonary Eosinophilia,Pulmonary Eosinophilia,,,,DOID:9498,pulmonary eosinophilia,C0034068,D011657,,MONDO:0004802,pulmonary eosinophilia,
+BMGC_DS02117,BMG_DS002733,,Pulmonary Fibrosis,Pulmonary Fibrosis,,,,DOID:3770,pulmonary fibrosis,C0034069,D011658,,MONDO:0002771,pulmonary fibrosis,
+BMGC_DS02118,BMG_DS002734,83291003,Cor pulmonale,,,,,DOID:8515,Cor pulmonale,C0034072,,MTHU007637,MONDO:0004596,cor pulmonale,Cor pulmonale | Cor pulmonale (disorder) | Pulmonary heart disease | Right heart failure due to pulmonary hypertension
+BMGC_DS02119,BMG_DS002735,,Pulmonary Infarction,Pulmonary Infarction,,,,,,C0034074,D054060,,MONDO:0004597,pulmonary embolism and infarction,
+BMGC_DS02120,BMG_DS002736,,,,,,,DOID:8861,pulmonary subvalvular stenosis,C0034084,,,MONDO:0006935,pulmonary subvalvular stenosis,
+BMGC_DS02121,BMG_DS002737,,,,,,,DOID:5749,pulmonary valve disease,C0034087,,,MONDO:0003628,pulmonary valve disorder,
+BMGC_DS02122,BMG_DS002738,,,,,,,DOID:14265,pulmonary valve insufficiency,C0034088,,,MONDO:0001927,pulmonary valve insufficiency,
+BMGC_DS02123,BMG_DS002739,,Pulmonary Valve Stenosis,Pulmonary Valve Stenosis,,,,DOID:6420,pulmonary valve stenosis,C0034089,D011666,,MONDO:0006936;MONDO:0020395,valvar pulmonary stenosis | pulmonary valve stenosis,
+BMGC_DS02124,BMG_DS002740,,,,,,,DOID:5453,pulmonary venoocclusive disease,C0034091,,,MONDO:0009937,pulmonary venoocclusive disease,
+BMGC_DS02125,BMG_DS002741,22361007,Pulp degeneration,,DA09.4,Pulp degeneration,K04.2,DOID:11189,pulp degeneration,C0034100,,,MONDO:0001216,pulp degeneration,Pulp degeneration | Pulp degeneration (disorder)
+BMGC_DS02126,BMG_DS002742,32620007;155638006,Pulpitis,Pulpitis,DA09.0,Pulpitis,K04.0,DOID:11121,pulpitis,C0034103,D011671,,MONDO:0006937,pulpitis,Pulpitis | Pulpitis (disorder)
+BMGC_DS02127,BMG_DS002743,,Pupil Disorders,Pupil Disorders,,,,DOID:238,pupil disease,C0034124,D011681,,MONDO:0002285,pupil disorder,
+BMGC_DS02128,BMG_DS002744,,"Purine-Pyrimidine Metabolism, Inborn Errors","Purine-Pyrimidine Metabolism, Inborn Errors",,,,,,C0034139,D011686,,MONDO:0019254,inborn disorder of purine or pyrimidine metabolism,
+BMGC_DS02129,BMG_DS002745,423902002;246989006;118653003;154822006;191313005;12393003;387778001;267564008,Purpura,Purpura,,,,DOID:3326,purpura,C0034150,D011693,MTHU002611,MONDO:0002610,purpura,Purpura | Purpura (disorder) | Purpura | Simple bruising | Purpura simplex (disorder) | Purpuric disorder | Disorder characterized by purpura | Disorder characterised by purpura | Purpura | Simple bruising | Purpuric disorder (disorder) | Purpura | Thrombocytopenic purp. | Thrombocytopenic purpura | (Purpura/hemorrhagic condition) or (purpura) or (thrombocytopenic purpura) | (Purpura/haemorrhagic condition) or (purpura) or (thrombocytopenic purpura) | Purpura/haemorrhagic condition | Purpura/hemorrhagic condition | (Purpura/haemorrhagic condition) or (purpura) or (thrombocytopenic purpura) (disorder) | Purpura | Purpura (morphologic abnormality) | Purpuric disorder (disorder) | Purpuric disorder | Disorder characterised by purpura | Disorder characterized by purpura | Purpura | Thrombocytopenic purpura | Purpura | Thrombocytopenic purp. | Purpura/haemorrhagic condition | (Purpura/haemorrhagic condition) or (purpura) or (thrombocytopenic purpura) | Purpura/hemorrhagic condition | (Purpura/hemorrhagic condition) or (purpura) or (thrombocytopenic purpura) | (Purpura/haemorrhagic condition) or (purpura) or (thrombocytopenic purpura) (disorder)
+BMGC_DS02130,BMG_DS002746,,"Purpura, Hyperglobulinemic","Purpura, Hyperglobulinemic",,,,DOID:3325,hyperglobulinemic purpura,C0034151,D011694,,MONDO:0006792,hyperglobulinemic purpura,
+BMGC_DS02131,BMG_DS002747,,Henoch-Schoenlein Purpura,IgA Vasculitis,,,,DOID:11123,Henoch-Schoenlein purpura,C0034152,D011695,,MONDO:0019167,immunoglobulin A vasculitis,
+BMGC_DS02132,BMG_DS002748,,"Purpura, Thrombotic Thrombocytopenic","Purpura, Thrombotic Thrombocytopenic",,,,DOID:10772,thrombotic thrombocytopenic purpura,C0034155,D011697,,MONDO:0018896,thrombotic thrombocytopenic purpura,
+BMGC_DS02133,BMG_DS002749,27174002,Pyelitis,Pyelitis,,,,DOID:2744,pyelitis,C0034183,D011702,,MONDO:0006938,pyelitis,Pyelitis | Pyelitis (disorder)
+BMGC_DS02134,BMG_DS002751,45816000,Pyelonephritis,Pyelonephritis,,,N16,DOID:11400,pyelonephritis,C0034186,D011704,MTHU042201,MONDO:0006939,pyelonephritis,Pyelonephritis | Pyelonephritis (disorder)
+BMGC_DS02135,BMG_DS002752,,"Pyelonephritis, Xanthogranulomatous","Pyelonephritis, Xanthogranulomatous",,,,DOID:11401,xanthogranulomatous pyelonephritis,C0034188,D011705,,MONDO:0007022,xanthogranulomatous pyelonephritis,
+BMGC_DS02136,BMG_DS002754,,,,,,,DOID:12639,pyloric stenosis,C0034194,,,MONDO:0001561,pyloric stenosis,
+BMGC_DS02137,BMG_DS002755,70759006;156323008;267838007,Pyoderma,Pyoderma,EB21,Pyoderma gangrenosum,L08.0,DOID:4223,pyoderma,C0034212,D011711,MTHU042265,MONDO:0002922,pyoderma,"Pyoderma | Pyodermia | Purulent dermatitis | Suppurative dermatitis | Septic dermatitis | Pyogenic dermatitis | Pustuloderma | Pyoderma (disorder) | Pyogenic infection of skin and subcutis | Pyogenic granuloma | Pyoderma | (Skin infection, localized NOS) or (pyoderma) or (pyogenic granuloma) | (Skin infection, localised NOS) or (pyoderma) or (pyogenic granuloma) | Skin infection, localized NOS | Skin infection, localised NOS | (Skin infection, localised NOS) or (pyoderma) or (pyogenic granuloma) (disorder) | (Skin infection, localized NOS) or (pyoderma) or (pyogenic granuloma) | Pyogenic granuloma | Pyoderma | Skin infection, localised NOS | (Skin infection, localised NOS) or (pyoderma) or (pyogenic granuloma) | Skin infection, localized NOS | (Skin infection, localised NOS) or (pyoderma) or (pyogenic granuloma) (disorder)"
+BMGC_DS02138,BMG_DS002759,266651008;397810006;9400007;35263009;155974004,Pyosalpinx,,,,,DOID:5732,pyosalpinx,C0034220,,,MONDO:0003618,pyosalpinx,"(Pelvic inflammatory disease: [NOS] or [chronic]) or (pyosalpinx) | Pelvic inflammatory disease NOS | Pelvic inflam. disease NOS | Chronic pelvic inflammatory disease | Pyosalpinx | Pelvic inflam disease,chronic | (Pelvic inflammatory disease: [NOS] or [chronic]) or (pyosalpinx) (disorder) | Pyosalpinx (disorder) | Pyosalpinx | Pyosalpingitis | Pyosalpingitis | Pyosalpingitis (disorder) | Abscess of fallopian tube | Pyosalpinx | Pyosalpingitis | Fallopian tube abscess | Abscess of fallopian tube (disorder) | Chronic pelvic inflammatory disease | Pelvic inflam disease,chronic | Pelvic inflammatory disease NOS | Pyosalpinx | Pelvic inflam. disease NOS | (Pelvic inflammatory disease: [NOS] or [chronic]) or (pyosalpinx) | (Pelvic inflammatory disease: [NOS] or [chronic]) or (pyosalpinx) (disorder)"
+BMGC_DS02139,BMG_DS002760,266627003;85884009,Pyoureter,,,,,DOID:1425,pyoureter,C0034223,,,MONDO:0001922,pyoureter,(Renal disease NOS) or (pyoureter) | Pyoureter | Renal disease NOS | (Renal disease NOS) or (pyoureter) (disorder) | Pyoureter | Pyoureter (disorder)
+BMGC_DS02140,BMG_DS002761,,Pyruvate Carboxylase Deficiency Disease,Pyruvate Carboxylase Deficiency Disease,,,,DOID:3651,pyruvate carboxylase deficiency disease,C0034341,D015324,266150,MONDO:0009949,pyruvate carboxylase deficiency disease,
+BMGC_DS02141,BMG_DS002762,,Pyruvate Dehydrogenase Complex Deficiency Disease,Pyruvate Dehydrogenase Complex Deficiency Disease,,,,DOID:3649,pyruvate decarboxylase deficiency,C0034345,D015325,,MONDO:0019169,pyruvate dehydrogenase deficiency,
+BMGC_DS02142,BMG_DS002763,,"Pyruvate Metabolism, Inborn Errors","Pyruvate Metabolism, Inborn Errors",,,,,,C0034350,D015323,,,,
+BMGC_DS02143,BMG_DS002764,,,,,,,DOID:1439,pyuria,C0034359,,,MONDO:0001953,pyuria,
+BMGC_DS02144,BMG_DS002765,,Q Fever,Q Fever,,,,DOID:11100,Q fever,C0034362,D011778,,MONDO:0019186,Q fever,
+BMGC_DS02145,BMG_DS002766,155030003;11538006,Quadriplegia,Quadriplegia,MB50.Z,"Tetraplegia, unspecified",G82.5,DOID:12835,quadriplegia,C0034372,D011782,MTHU038030,MONDO:0001590,quadriplegia,Quadriplegia | Quadriplegia (disorder) | Quadriplegia | Tetraplegia | Quadriplegia (disorder)
+BMGC_DS02146,BMG_DS002767,14168008,Rabies (disorder),,,,,DOID:11260,rabies,C0034494,,,MONDO:0019173,rabies,Rabies | Hydrophobia | Lyssa | Rabies (disorder)
+BMGC_DS02147,BMG_DS002768,,Radiation Syndrome,Radiation Injuries,,,,,,C0034535,D011832,,MONDO:0043458,radiation injury,
+BMGC_DS02148,BMG_DS002769,82473003;123255000,Radiculitis,Radiculopathy,,,,,,C0034544,D011843,,MONDO:0021765,radiculitis,Radiculitis | Radiculitis (disorder) | Radiculitis (disorder) | Radiculitis
+BMGC_DS02149,BMG_DS002770,,Radiation-Induced Dermatitis,Radiodermatitis,,,,,,C0034561,D011855,,MONDO:0043771,radiodermatitis,
+BMGC_DS02150,BMG_DS002772,,Rat-Bite Fever,Rat-Bite Fever,,,,,,C0034686,D011906,,MONDO:0006941,rat-bite fever,
+BMGC_DS02151,BMG_DS002773,,Raynaud Disease,Raynaud Disease,,,,DOID:10300,Raynaud disease,C0034734,D011928,179600,MONDO:0008364,Raynaud disease,
+BMGC_DS02152,BMG_DS002774,,Raynaud Phenomenon,Raynaud Disease,,,,,,C0034735,D011928,,,,
+BMGC_DS02153,BMG_DS002776,,Rectal Diseases,Rectal Diseases,,,,DOID:1285,rectal disease,C0034882,D012002,,MONDO:0001593,rectal disorder,
+BMGC_DS02154,BMG_DS002777,,,,,,,DOID:1984,rectal benign neoplasm,C0034885,,,MONDO:0002165,rectal neoplasm,
+BMGC_DS02155,BMG_DS002779,,Rectal Prolapse,Rectal Prolapse,,,,DOID:9307,rectal prolapse,C0034888,D012005,,MONDO:0004754,rectal prolapse,
+BMGC_DS02156,BMG_DS002780,,Pure Red-Cell Aplasia,"Red-Cell Aplasia, Pure",,,,DOID:1340,pure red-cell aplasia,C0034902,D012010,,MONDO:0001705,pure red-cell aplasia,
+BMGC_DS02157,BMG_DS002782,,Reflex Sympathetic Dystrophy,Reflex Sympathetic Dystrophy,,,,DOID:1811,reflex sympathetic dystrophy,C0034931,D012019,604335,MONDO:0011441,complex regional pain syndrome type 1,
+BMGC_DS02158,BMG_DS002783,,Refractive Errors,Refractive Errors,,,,DOID:9835,refractive error,C0034951,D012030,,MONDO:0004892,refractive error,
+BMGC_DS02159,BMG_DS002784,,Refsum Disease,Refsum Disease,,,,DOID:10582,Refsum disease,C0034960,D012035,600964;266500,MONDO:0009958,adult Refsum disease,
+BMGC_DS02160,BMG_DS002785,,Reiter Syndrome,"Arthritis, Reactive",,,,DOID:6196,reactive arthritis,C0035012,D016918,,,,
+BMGC_DS02161,BMG_DS002786,,Relapsing Fever,Relapsing Fever,,,,DOID:13034,relapsing fever,C0035021,D012061,,MONDO:0019633,relapsing fever,
+BMGC_DS02162,BMG_DS002787,10301003,Tick-borne relapsing fever,,1C1J.0,Tickborne relapsing fever,A68.1,DOID:13036,tick-borne relapsing fever,C0035022,,,MONDO:0001621,tick-borne relapsing fever,Tick-borne relapsing fever | Tick-borne relapsing fever (disorder)
+BMGC_DS02163,BMG_DS002788,,Renal Artery Obstruction,Renal Artery Obstruction,,,,DOID:2972,renal artery obstruction,C0035066,D012078,,MONDO:0006945,renal artery obstruction,
+BMGC_DS02164,BMG_DS002789,,Renal Artery Stenosis,Renal Artery Obstruction,,,,,,C0035067,D012078,,,,
+BMGC_DS02165,BMG_DS002790,,Kidney Failure,Renal Insufficiency,,,,DOID:1074,kidney failure,C0035078,D051437,,MONDO:0001106,kidney failure,
+BMGC_DS02166,BMG_DS002792,,Renal Osteodystrophy,Chronic Kidney Disease-Mineral and Bone Disorder,,,,DOID:13068,renal osteodystrophy,C0035086,D012080,,MONDO:0006946,renal osteodystrophy,
+BMGC_DS02167,BMG_DS002793,,"Renal Tubular Transport, Inborn Errors","Renal Tubular Transport, Inborn Errors",,,,DOID:447,renal tubular transport disease,C0035091,D015499,,MONDO:0006510,renal tubular transport disease,
+BMGC_DS02168,BMG_DS002796,,Respiration Disorders,Respiration Disorders,,,,,,C0035204,D012120,,MONDO:0005087,respiratory system disorder,
+BMGC_DS02169,BMG_DS002797,,"Respiratory Distress Syndrome, Newborn","Respiratory Distress Syndrome, Newborn",,,,,,C0035220,D012127,,MONDO:0100077,congenital alveolar dysplasia,
+BMGC_DS02170,BMG_DS002798,,"Respiratory Distress Syndrome, Adult",Respiratory Distress Syndrome,,,,DOID:11394,adult respiratory distress syndrome,C0035222,D012128,,MONDO:0100130,adult acute respiratory distress syndrome,
+BMGC_DS02171,BMG_DS002800,,Respiratory Syncytial Virus Infections,Respiratory Syncytial Virus Infections,,,,DOID:1273,respiratory syncytial virus infectious disease,C0035235,D018357,,MONDO:0001577,respiratory syncytial virus infectious disease,
+BMGC_DS02172,BMG_DS002801,,Respiratory Tract Diseases,Respiratory Tract Diseases,,,,,,C0035242,D012140,,,,
+BMGC_DS02173,BMG_DS002802,,Respiratory Tract Infections,Respiratory Tract Infections,,,,,,C0035243,D012141,,MONDO:0024355,respiratory tract infectious disorder,
+BMGC_DS02174,BMG_DS002804,,Restless Legs Syndrome,Restless Legs Syndrome,,,,DOID:0050425,restless legs syndrome,C0035258,D012148,,MONDO:0005391,restless legs syndrome,
+BMGC_DS02175,BMG_DS002806,,,,,,,DOID:1731,histoplasmosis,C0035288,,312500,MONDO:0010721,"reticuloendotheliosis, X-linked",
+BMGC_DS02176,BMG_DS002807,,,,,,,DOID:4394,reticulohistiocytic granuloma,C0035290,,,MONDO:0002984,reticulohistiocytic granuloma,
+BMGC_DS02177,BMG_DS002808,,Retinal Artery Occlusion,Retinal Artery Occlusion,,,,DOID:8483,retinal artery occlusion,C0035302,D015356,,MONDO:0006948,retinal artery occlusion,
+BMGC_DS02178,BMG_DS002809,,,,,,,DOID:8466,retinal degeneration,C0035304,,,MONDO:0004580,retinal degeneration,
+BMGC_DS02179,BMG_DS002810,,Retinal Detachment,Retinal Detachment,,,,DOID:5327,retinal detachment,C0035305,D012163,312530;180050,MONDO:0008375,retinal detachment,
+BMGC_DS02180,BMG_DS002811,,Retinal Diseases,Retinal Diseases,,,,DOID:5679,retinal disease,C0035309,D012164,,MONDO:0005283,retinal disorder,
+BMGC_DS02181,BMG_DS002812,,Retinal Drusen,Retinal Drusen,,,,DOID:2569,retinal drusen,C0035312,D015593,,MONDO:0006949,retinal drusen,
+BMGC_DS02182,BMG_DS002813,,"Retinal Necrosis Syndrome, Acute","Retinal Necrosis Syndrome, Acute",,,,DOID:3611,acute retinal necrosis syndrome,C0035319,D015882,,MONDO:0006638,acute retinal necrosis syndrome,
+BMGC_DS02183,BMG_DS002814,,Retinal Perforations,Retinal Perforations,,,,DOID:12514,retinal perforation,C0035321,D012167,,MONDO:0001539,retinal perforation,
+BMGC_DS02184,BMG_DS002815,155111000;73757007;267717005,Retinal vascular occlusion,,,,,DOID:1729,retinal vascular occlusion,C0035326,,,MONDO:0002089,retinal vascular occlusion,(Retinal vascular occlusion) or (amaurosis fugax) or (retinal thrombosis) | Retinal vasc. occlusion | Retinal vascular occlusion | Amaurosis fugax | Retinal thrombosis | (Retinal vascular occlusion) or (amaurosis fugax) or (retinal thrombosis) (disorder) | Retinal vascular occlusion | Retinal vascular occlusion (disorder) | (Retinal vascular occlusion) or (amaurosis fugax) or (retinal thrombosis) | Retinal vascular occlusion | Retinal vasc. occlusion | Amaurosis fugax | Retinal thrombosis | (Retinal vascular occlusion) or (amaurosis fugax) or (retinal thrombosis) (disorder)
+BMGC_DS02185,BMG_DS002816,,Retinal Vein Occlusion,Retinal Vein Occlusion,,,,DOID:1727,retinal vein occlusion,C0035328,D012170,,MONDO:0006951,retinal vein occlusion,
+BMGC_DS02186,BMG_DS002817,35426003;399463004,Retinitis,Retinitis,,,,DOID:3612,retinitis,C0035333,D012173,MTHU047424,MONDO:0002708,retinitis,Retinitis | Retinopathy | Retinitis (disorder) | Retinitis (disorder) | Retinitis
+BMGC_DS02187,BMG_DS002818,,Retinitis Pigmentosa,Retinitis Pigmentosa,,,,DOID:10584,retinitis pigmentosa,C0035334,D012174,268000,MONDO:0019200,retinitis pigmentosa,
+BMGC_DS02188,BMG_DS002819,,,,,,,DOID:768,retinoblastoma,C0035335,,,MONDO:0008380,retinoblastoma,
+BMGC_DS02189,BMG_DS002820,,Retinopathy of Prematurity,Retinopathy of Prematurity,,,,DOID:13025,retinopathy of prematurity,C0035344,D012178,,MONDO:0006952,retinopathy of prematurity,
+BMGC_DS02190,BMG_DS002821,,Retrocochlear Diseases,Retrocochlear Diseases,,,,DOID:2889,retrocochlear disease,C0035352,D012181,,MONDO:0002453,retrocochlear disease,
+BMGC_DS02191,BMG_DS002822,155873006;266626007;49120005,Retroperitoneal fibrosis,,,,K68.2,,,C0035357,,MTHU068355,MONDO:0018848,IgG4-related retroperitoneal fibrosis,(Ureter obstruction &/or stricture) or (retroperitoneal fibrosis) | Ureter stricture/obstruction | Ureter - stricture | Stricture of ureter | Retroperitoneal fibrosis | Stricture - ureter | (Ureter obstruction &/or stricture) or (retroperitoneal fibrosis) (disorder) | Stricture - ureter | Ureter - stricture | Stricture of ureter | Ureter stricture/obstruction | Retroperitoneal fibrosis | (Ureter obstruction &/or stricture) or (retroperitoneal fibrosis) | (Ureter obstruction &/or stricture) or (retroperitoneal fibrosis) (disorder) | Retroperitoneal fibrosis | Ormond's disease | Sclerosing retroperitonitis | RPF - Retroperitoneal fibrosis | Retroperitoneal fibrosis (disorder)
+BMGC_DS02192,BMG_DS002823,,,,,,,DOID:5875,retroperitoneal cancer,C0035358,,,MONDO:0024645,retroperitoneal neoplasm,
+BMGC_DS02193,BMG_DS002825,,Rett Syndrome,Rett Syndrome,,,,DOID:1206,Rett syndrome,C0035372,D015518,312750,MONDO:0010726,Rett syndrome,
+BMGC_DS02194,BMG_DS002826,,Reye Syndrome,Reye Syndrome,,,,DOID:14525,Reye syndrome,C0035400,D012202,,MONDO:0005942,Reye syndrome,
+BMGC_DS02195,BMG_DS002827,,Rh Isoimmunization,,,,,DOID:4175,Rh isoimmunization,C0035404,D012203,,MONDO:0006953,Rh isoimmunization,
+BMGC_DS02196,BMG_DS002829,,,,,,,DOID:3247,rhabdomyosarcoma,C0035412,,,MONDO:0005212,rhabdomyosarcoma,
+BMGC_DS02197,BMG_DS002830,29913006;396332003,Rheumatism,Rheumatic Diseases,,,,,,C0035435,D012216,,,,Rheumatism | Non-articular rheumatism | Musculoskeletal pain disorder | NAR - Non-articular rheumatism | Locomotor pain disorder | Soft tissue rheumatism | Rheumatism (disorder) | Rheumatism (disorder) | Rheumatism | Locomotor pain disorder | Musculoskeletal pain disorder
+BMGC_DS02198,BMG_DS002831,,Rheumatic Fever,Rheumatic Fever,,,,DOID:1586,rheumatic fever,C0035436,D012213,,MONDO:0017767,rheumatic fever,
+BMGC_DS02199,BMG_DS002832,,Rheumatic Heart Disease,Rheumatic Heart Disease,,,,DOID:0050827,rheumatic heart disease,C0035439,D012214,,MONDO:0006955,rheumatic heart disease,
+BMGC_DS02200,BMG_DS002833,8805001;312591002,Acute rheumatic heart disease,,,,,DOID:8481,rheumatic myocarditis,C0035440,,,MONDO:0021777,acute rheumatic heart disease,Acute rheumatic heart disease | Acute rheumatic heart disease (disorder) | Acute rheumatic heart disease | Acute rheumatic fever with heart involvement | Active rheumatic fever with heart involvement | Acute rheumatic fever with heart disease (disorder) | Acute rheumatic fever with heart disease
+BMGC_DS02201,BMG_DS002836,70076002,Rhinitis,Rhinitis,,,,DOID:4483,rhinitis,C0035455,D012220,MTHU012038,MONDO:0003014,rhinitis,Rhinitis | Irritation of nose | Rhinitis (disorder)
+BMGC_DS02202,BMG_DS002837,,"Rhinitis, Allergic, Perennial","Rhinitis, Allergic, Perennial",,,,,,C0035457,D012221,,MONDO:0024332,perennial allergic rhinitis,
+BMGC_DS02203,BMG_DS002838,,"Rhinitis, Atrophic","Rhinitis, Atrophic",,,,DOID:4731,atrophic rhinitis,C0035459,D012222,,MONDO:0005659,atrophic rhinitis,
+BMGC_DS02204,BMG_DS002839,,"Rhinitis, Vasomotor","Rhinitis, Vasomotor",,,,DOID:4730,vasomotor rhinitis,C0035460,D012223,,MONDO:0006004,vasomotor rhinitis,
+BMGC_DS02205,BMG_DS002841,72409005,Rhinoscleroma,Rhinoscleroma,,,,DOID:11336,rhinoscleroma,C0035468,D012226,,MONDO:0005945,rhinoscleroma,Rhinoscleroma | Infection by Klebsiella rhinoscleromatis | Scleroma | Rhinoscleroma (disorder)
+BMGC_DS02206,BMG_DS002843,,Riboflavin Deficiency,Riboflavin Deficiency,,,,DOID:8454,riboflavin deficiency,C0035528,D012257,,,,
+BMGC_DS02207,BMG_DS002844,190639009;154728003;41345002,Rickets,Rickets,,,,DOID:10609,rickets,C0035579,D012279,MTHU006645,MONDO:0005520,rickets,Vitamin D deficiency | Osteomalacia | Rickets | (Vitamin D deficiency) or (osteomalacia) or (rickets) | (Vitamin D deficiency) or (osteomalacia) or (rickets) (disorder) | Osteomalacia | Vitamin D deficiency | Rickets | (Vitamin D deficiency) or (osteomalacia) or (rickets) | (Vitamin D deficiency) or (osteomalacia) or (rickets) (disorder) | Rickets | Rickets (disorder)
+BMGC_DS02208,BMG_DS002845,,Rickettsia Infections,Rickettsia Infections,,,,,,C0035585,D012282,,MONDO:0006956,Rickettsiosis,
+BMGC_DS02209,BMG_DS002847,75096007,Rickettsialpox,Spotted Fever Group Rickettsiosis,,,,DOID:11103,rickettsialpox,C0035597,D000073605,,MONDO:0019360,rickettsialpox,Rickettsialpox | Vesicular rickettsiosis | Rickettsialpox due to Rickettsia akari | Kew Gardens spotted fever | Rickettsialpox (disorder)
+BMGC_DS02210,BMG_DS002848,,Rift Valley Fever,Rift Valley Fever,,,,DOID:1328,Rift Valley fever,C0035613,D012295,,MONDO:0017880,Rift valley fever,
+BMGC_DS02211,BMG_DS002849,,,,,,,,,C0035615,,,MONDO:0020417,right aortic arch,
+BMGC_DS02212,BMG_DS002852,,,,,,,DOID:0070620,ring chromosome syndrome,C0035639,,,,,
+BMGC_DS02213,BMG_DS002854,,Rocky Mountain Spotted Fever,Rocky Mountain Spotted Fever,,,,DOID:0050052,Rocky Mountain spotted fever,C0035793,D012373,,MONDO:0019359,Rocky mountain spotted fever,
+BMGC_DS02214,BMG_DS002855,,Rodent Diseases,Rodent Diseases,,,,,,C0035801,D012376,,MONDO:0024981,rodent disease,
+BMGC_DS02215,BMG_DS002856,,Root Resorption,Root Resorption,,,,DOID:14550,root resorption,C0035851,D012391,,MONDO:0001997,root resorption,
+BMGC_DS02216,BMG_DS002857,200930009;267849001;1612004;156364003;398909004,Rosacea,Rosacea,,,L71,DOID:8881,rosacea,C0035854,D012393,MTHU064119,MONDO:0006604,rosacea,Rosacea | Rosacea (disorder) | (Acne roscea) or (acne rosacea) or (rhinophyma) or (rosacea) | Acne rosacea | Acne roscea | Rhinophyma | Rosacea | (Acne roscea) or (acne rosacea) or (rhinophyma) or (rosacea) (disorder) | Acne rosacea | Rosacea | Acne erythematosa | Acne rosacea (disorder) | (Acne roscea) or (acne rosacea) or (rhinophyma) or (rosacea) | Acne roscea | Acne rosacea | Rosacea | Rhinophyma | (Acne roscea) or (acne rosacea) or (rhinophyma) or (rosacea) (disorder) | Rosacea (disorder) | Rosacea | Acne rosacea | Acne erythematosa
+BMGC_DS02217,BMG_DS002858,,Rotavirus Infections,Rotavirus Infections,,,,,,C0035869,D012400,,MONDO:0005194,Rotavirus infection,
+BMGC_DS02218,BMG_DS002859,154343004;266192003;36653000,Rubella,Rubella,,,,DOID:8781,rubella,C0035920,D012409,,MONDO:0004656,rubella,(Rubella [& German measles]) or (Roseola) | Roseola | German measles | Rubella | (Rubella [& German measles]) or (Roseola) (disorder) | (Rubella [& German measles]) or (Roseola) | German measles | Rubella | Roseola | (Rubella [& German measles]) or (Roseola) (disorder) | Rubella | German measles | Rubella (disorder)
+BMGC_DS02219,BMG_DS002861,,Rubinstein-Taybi Syndrome,Rubinstein-Taybi Syndrome,,,,DOID:1933,Rubinstein-Taybi syndrome,C0035934,D012415,,MONDO:0019188,Rubinstein-Taybi syndrome,
+BMGC_DS02220,BMG_DS002862,,Saldino-Noonan Syndrome,Short Rib-Polydactyly Syndrome,,,,,,C0036069,D012779,613091,MONDO:0013127,asphyxiating thoracic dystrophy 3,
+BMGC_DS02221,BMG_DS002864,28826002;155656006,Sialolithiasis,Salivary Gland Calculi,DA04.4,Sialolithiasis,K11.5,DOID:12905,sialolithiasis,C0036091,D015494,,MONDO:0006970,sialolithiasis,Sialolithiasis | Calculus of salivary gland | Stone of salivary gland | Salivary calculus | Sialolith | Salivary stone | Sialolithiasis (disorder) | Sialolithiasis | Sialolithiasis (disorder)
+BMGC_DS02222,BMG_DS002865,,Salivary Gland Diseases,Salivary Gland Diseases,,,,,,C0036093,D012466,,,,
+BMGC_DS02223,BMG_DS002866,,,,,,,,,C0036095,,,MONDO:0021357,tumor of salivary gland,
+BMGC_DS02224,BMG_DS002867,42338000;186094005;302229004,Salmonella food poisoning,,,,,,,C0036114,,,MONDO:0005950,Salmonella gastroenteritis,Salmonella gastroenteritis | Enteric paratyphosis | Salmonella gastroenteritis (disorder) | Salmonellosis (& [gastroenteritis] or [food poisoning]) | Salmonella food poisoning | Salmonellosis | Salmonella gastroenteritis | Salmonellosis (& [gastroenteritis] or [food poisoning]) (disorder) | Salmonella food poisoning | Salmonella food poisoning (disorder)
+BMGC_DS02225,BMG_DS002868,,,,,,,,,C0036117,,,MONDO:0000827,salmonellosis,
+BMGC_DS02226,BMG_DS002869,,"Salmonella Infections, Animal","Salmonella Infections, Animal",,,,,,C0036118,D012481,,MONDO:0024982,"salmonella infections, animal",
+BMGC_DS02227,BMG_DS002870,88157006;266648001;155968004,Salpingitis,Salpingitis,,,,DOID:5733,salpingitis,C0036130,D012488,,MONDO:0003619,salpingitis,Salpingitis | Salpingitis (disorder) | Inflammation of fallopian tube | Pelvic inflammatory disease (& [chronic NOS] or [oophoritis] or [salpingitis]) | Pelvic inflammatory disease | Inflam. dis.- pelvic | Chronic pelvic inflam. dis.NOS | Oophoritis | Salpingitis | Pelvic inflammatory disease (& [chronic NOS] or [oophoritis] or [salpingitis]) (disorder) | Pelvic inflammatory disease (& [chronic NOS] or [oophoritis] or [salpingitis]) | Chronic pelvic inflam. dis.NOS | Pelvic inflammatory disease | Salpingitis | Oophoritis | Inflam. dis.- pelvic | Pelvic inflammatory disease (& [chronic NOS] or [oophoritis] or [salpingitis]) (disorder)
+BMGC_DS02228,BMG_DS002871,46536000,Tubo-ovarian inflammatory disease,,,,,DOID:10972,salpingo-oophoritis,C0036133,,,MONDO:0001172,salpingo-oophoritis,Tubo-ovarian inflammatory disease | Salpingo-oophoritis | Tubo-ovarian inflammatory disease (disorder) | Inflammation of ovary and fallopian tube | Salpingitis and oophoritis
+BMGC_DS02229,BMG_DS002872,,Sandhoff Disease,Sandhoff Disease,,,,DOID:3323,Sandhoff disease,C0036161,D012497,268800,MONDO:0010006,Sandhoff disease,
+BMGC_DS02230,BMG_DS002873,154425004;31541009,Sarcoidosis,Sarcoidosis,,,D86,DOID:11335,sarcoidosis,C0036202,D012507,MTHU070178,MONDO:0019338,sarcoidosis,Sarcoidosis | Sarcoidosis (disorder) | Sarcoidosis | Boeck's sarcoid | Besnier-Boeck-Schaumann syndrome | Miliary lupoid of Boeck | Lupus pernio of Besnier | Benign lymphogranulomatosis of Schaumann | Darier-Roussy sarcoid | Sarcoidosis (disorder) | Boeck's sarcoidosis
+BMGC_DS02231,BMG_DS002874,55941000,Cutaneous sarcoidosis,,,,,DOID:13402,skin sarcoidosis,C0036203,,,MONDO:0006611,skin sarcoidosis,Cutaneous sarcoidosis | Cutaneous sarcoidosis (disorder) | Sarcoidosis of skin | Skin sarcoidosis
+BMGC_DS02232,BMG_DS002876,,"Sarcoidosis, Pulmonary","Sarcoidosis, Pulmonary",,,,DOID:13406,pulmonary sarcoidosis,C0036205,D017565,,MONDO:0001708,pulmonary sarcoidosis,
+BMGC_DS02233,BMG_DS002880,,,,,,,DOID:8632,Kaposi's sarcoma,C0036220,,,MONDO:0005055,Kaposi's sarcoma,
+BMGC_DS02234,BMG_DS002881,,,,,,,DOID:355,mast-cell sarcoma,C0036221,,,MONDO:0019024,mast cell sarcoma,
+BMGC_DS02235,BMG_DS002882,88905005,Sarcocystosis,Sarcocystosis,1A3Z,"Protozoal intestinal infections, unspecified",A07.8,DOID:9640,sarcocystosis,C0036231,D012523,,MONDO:0018903,sarcocystosis,Sarcosporidiosis | Sarcosporidiasis | Sarcocystosis | Sarcosporidiosis (disorder) | Sarcocystiosis
+BMGC_DS02236,BMG_DS002883,,,,,,,DOID:8295,scabies,C0036262,,,MONDO:0004525,scabies,
+BMGC_DS02237,BMG_DS002884,,Scalp Dermatoses,Scalp Dermatoses,,,,DOID:3136,scalp dermatosis,C0036271,D012536,,MONDO:0006605,scalp dermatosis,
+BMGC_DS02238,BMG_DS002886,,Scarlet Fever,Scarlet Fever,,,,DOID:8596,scarlet fever,C0036285,D012541,,MONDO:0005952,scarlet fever,
+BMGC_DS02239,BMG_DS002887,,Schamberg Disease,Pigmentation Disorders,,,,,,C0036305,D010859,,MONDO:0006562,obsolete incontinentia pigmenti achromians,
+BMGC_DS02240,BMG_DS002888,,Scheuermann's Disease,Scheuermann Disease,,,,DOID:13300,Scheuermann's disease,C0036310,D012544,181440,MONDO:0008410,Scheuermann disease,
+BMGC_DS02241,BMG_DS002889,266222003;10087007;154415009,Schistosomiasis,Schistosomiasis,,,,,,C0036323,D012552,,MONDO:0015254,schistosomiasis,(Other helminthiases (& [oxyuriasis] or [schistosomiasis] or [taenia infestation] or [trichinosis])) or ([filaria] or [flukes] or [tapeworms] or [toxocara]) | Oxyuriasis | Filaria | Toxocara | Other helminthiases | Trichinosis | Schistosomiasis | Taenia infestation | Flukes | Tapeworms | (Other helminthiases (& [oxyuriasis] or [schistosomiasis] or [taenia infestation] or [trichinosis])) or ([filaria] or [flukes] or [tapeworms] or [toxocara]) (disorder) | Infection by Schistosoma | Schistosomiasis | Bilharziasis | Hemic distomiasis | Schistosomosis | Bilharzia | Schistosomiasis - bilharziasis | Blood fluke infection | Haemic distomiasis | Infection caused by Schistosoma (disorder) | Infection caused by Schistosoma | (Other helminthiases (& [oxyuriasis] or [schistosomiasis] or [taenia infestation] or [trichinosis])) or ([filaria] or [flukes] or [tapeworms] or [toxocara]) | Oxyuriasis | Tapeworms | Taenia infestation | Flukes | Other helminthiases | Filaria | Schistosomiasis | Trichinosis | Toxocara | (Other helminthiases (& [oxyuriasis] or [schistosomiasis] or [taenia infestation] or [trichinosis])) or ([filaria] or [flukes] or [tapeworms] or [toxocara]) (disorder)
+BMGC_DS02242,BMG_DS002890,,Schistosomiasis japonica,Schistosomiasis japonica,,,,DOID:0050597,intestinal schistosomiasis,C0036329,D012554,,MONDO:0044344,Schistosoma japonicum infectious disease | ,
+BMGC_DS02243,BMG_DS002891,,Schistosomiasis mansoni,Schistosomiasis mansoni,,,,DOID:0050597,intestinal schistosomiasis,C0036330,D012555,,MONDO:0044345,Schistosoma mansoni infectious disease | ,
+BMGC_DS02244,BMG_DS002894,,,,,,,DOID:5418,schizoaffective disorder,C0036337,,,MONDO:0005487,schizoaffective disorder,
+BMGC_DS02245,BMG_DS002895,,,,,,,DOID:10936,schizoid personality disorder,C0036339,,,MONDO:0001161,schizoid personality disorder,
+BMGC_DS02246,BMG_DS002896,,,,,,,DOID:5419,schizophrenia,C0036341,,181500,MONDO:0005090,schizophrenia,
+BMGC_DS02247,BMG_DS002897,,,,,,,,,C0036346,,,MONDO:0957430,childhood-onset schizophrenia,
+BMGC_DS02248,BMG_DS002898,,,,,,,DOID:1229,paranoid schizophrenia,C0036349,,,MONDO:0001484,paranoid schizophrenia,
+BMGC_DS02249,BMG_DS002899,,,,,,,DOID:11328,schizophreniform disorder,C0036358,,,MONDO:0001265,schizophreniform disorder,
+BMGC_DS02250,BMG_DS002900,,,,,,,DOID:10646,schizotypal personality disorder,C0036363,,,,,
+BMGC_DS02251,BMG_DS002901,,Schwartz-Jampel Syndrome,Osteochondrodysplasias,,,,,,C0036391,D010009,,MONDO:0009717,Schwartz-Jampel syndrome,
+BMGC_DS02252,BMG_DS002903,,Scimitar Syndrome,Scimitar Syndrome,,,,DOID:4297,scimitar syndrome,C0036400,D012587,,MONDO:0015987,scimitar syndrome,
+BMGC_DS02253,BMG_DS002904,,Scleral Diseases,Scleral Diseases,,,,DOID:11343,scleral disease,C0036412,D015422,,MONDO:0001269,scleral disorder,
+BMGC_DS02254,BMG_DS002905,,Scleredema Adultorum,Scleredema Adultorum,,,,DOID:3140,scleredema adultorum,C0036413,D012592,,MONDO:0006606,scleredema adultorum,
+BMGC_DS02255,BMG_DS002907,194139000;155201000;78370002,Scleritis,Scleritis,9B51,Scleritis,H15.0,DOID:13452,scleritis,C0036416,D015423,,MONDO:0001718,scleritis,Scleritis &/or episcleritis | Scleritis and episcleritis | Scleritis | Episcleritis | Scleritis/episcleritis | Scleritis &/or episcleritis (disorder) | Scleritis/episcleritis | Scleritis | Episcleritis | Scleritis and episcleritis | Scleritis &/or episcleritis | Scleritis &/or episcleritis (disorder) | Scleritis | Scleritis (disorder) | Inflammation of white of eye
+BMGC_DS02256,BMG_DS002908,201048007;90424004,Localized scleroderma,,,,,DOID:8472,localized scleroderma,C0036420,,,MONDO:0019562,localized scleroderma,Localized dermatosclerosis | Morphea scleroderma | Localised scleroderma | Circumscribed scleroderma | Addison's keloid | Localized scleroderma | Localized morphea | Morphoea scleroderma | Localised dermatosclerosis | Localised morphoea | Localized morphea (disorder) | Localized scleroderma | Localised scleroderma | Localized scleroderma (disorder)
+BMGC_DS02257,BMG_DS002909,,Systemic Scleroderma,"Scleroderma, Systemic",,,,DOID:418,systemic scleroderma,C0036421,D012595,,MONDO:0005100,systemic sclerosis,
+BMGC_DS02258,BMG_DS002910,,"Scoliosis, unspecified",,FA70.1,Scoliosis,M41.9,DOID:0060249,scoliosis,C0036439,,,MONDO:0005392,scoliosis,
+BMGC_DS02259,BMG_DS002911,,,,,,,,,C0036454,,,MONDO:0004758,scotoma,
+BMGC_DS02260,BMG_DS002912,35103004,Scrapie,Scrapie,,,,DOID:5434,scrapie,C0036457,D012608,,MONDO:0006961,scrapie,Scrapie | Scrapie (disorder)
+BMGC_DS02261,BMG_DS002913,,Screw Worm Infection,Screw Worm Infection,,,,DOID:12927,screw worm infectious disease,C0036465,D012610,,MONDO:0005954,screw worm infectious disease,
+BMGC_DS02262,BMG_DS002915,,Scrub Typhus,Scrub Typhus,,,,DOID:13371,scrub typhus,C0036472,D012612,,MONDO:0019365,scrub typhus,
+BMGC_DS02263,BMG_DS002916,190638001;267493006;154727008;238129003;76169001,Scurvy,Scurvy,,,E54,DOID:13724,scurvy,C0036474,D012614,240400,MONDO:0009412,scurvy,(Ascorbic acid (vitamin C) deficiency) or (scurvy) | Ascorbic acid (vitamin C) deficiency | Vitamin C deficiency | Scurvy | (Ascorbic acid (vitamin C) deficiency) or (scurvy) (disorder) | Ascorbic acid deficiency (& [scurvy]) | Ascorbic acid deficiency | Ascorbic acid defic. | Scurvy | Ascorbic acid deficiency (& [scurvy]) (disorder) | Scurvy | Scurvy (disorder) | Ascorbic acid deficiency | Scurvy | Vitamin C deficiency | Ascorbic acid deficiency (disorder) | Deficiency of ascorbic acid
+BMGC_DS02264,BMG_DS002917,,Sea-Blue Histiocyte Syndrome,Sea-Blue Histiocyte Syndrome,,,,DOID:4423,sea-blue histiocytosis,C0036489,D012618,269600,MONDO:0010017,sea-blue histiocyte syndrome,
+BMGC_DS02265,BMG_DS002918,,Seasickness,Motion Sickness,NF08.3,Motion sickness,T75.3,,,C0036494,D009041,,,,
+BMGC_DS02266,BMG_DS002919,,Sebaceous Gland Diseases,Sebaceous Gland Diseases,,,,,,C0036502,D012625,,MONDO:0006607,sebaceous gland disorder,
+BMGC_DS02267,BMG_DS002920,,,,,,,DOID:5759,sebaceous gland neoplasm,C0036503,,,MONDO:0006963,sebaceous gland neoplasm,
+BMGC_DS02268,BMG_DS002921,156328004;200764003;50563003,Seborrheic dermatitis,,,,L21,DOID:8741,seborrheic dermatitis,C0036508,,MTHU011118,MONDO:0006608,seborrheic dermatitis,Seborrheic dermatitis | Seborrhoeic dermatitis | Seborrhoeic dermatitis (disorder) | Seborrhoeic dermatitis (& capitis) | Seborrhoeic dermatitis | Seborrhoeic dermatitis capitis | Seborrhoeic eczema | Seborrheic dermatitis | Seborrheic eczema | Seborrheic dermatitis capitis | Seborrheic dermatitis (& capitis) | Seborrhoeic dermatitis (& capitis) (disorder) | Seborrheic dermatitis | Seborrheic eczema | Seborrhoeic dermatitis | Seborrhoeic eczema | Seborrheic dermatitis (disorder) | SBD - Seborrhoeic dermatitis | SBD - Seborrheic dermatitis
+BMGC_DS02269,BMG_DS002922,,"Myocardial Diseases, Secondary",Cardiomyopathies,,,,DOID:0050700,cardiomyopathy,C0036529,D009202,,,,
+BMGC_DS02270,BMG_DS002923,,,,,,,DOID:5842;DOID:4440,seminoma | testis seminoma,C0036631,,,MONDO:0003001,seminoma,
+BMGC_DS02271,BMG_DS002924,,,,,,,DOID:9669,senile cataract,C0036646,,,MONDO:0004847,senile cataract,
+BMGC_DS02272,BMG_DS002926,,Sensation Disorders,Sensation Disorders,,,,,,C0036659,D012678,,,,
+BMGC_DS02273,BMG_DS002930,105592009;154313001,Septicemia,Sepsis,,,,,,C0036690,D018805,MTHU043659,,,Septicemia | Septicaemia | Septicemia (disorder) | Septicemia | Septicaemia | Septicaemia (disorder)
+BMGC_DS02274,BMG_DS002932,,,,,,,DOID:3577,Sertoli cell tumor,C0036769,,,MONDO:0002696,Sertoli cell tumor,
+BMGC_DS02275,BMG_DS002933,,Serum Sickness,Serum Sickness,,,,,,C0036830,D012713,,MONDO:0043789,serum sickness,
+BMGC_DS02276,BMG_DS002934,,Setariasis,Setariasis,,,,DOID:1079,setariasis,C0036850,D012719,,MONDO:0005957,setariasis,
+BMGC_DS02277,BMG_DS002935,,Sex Chromosome Aberrations,Sex Chromosome Aberrations,,,,,,C0036868,D012729,,,,
+BMGC_DS02278,BMG_DS002936,,,,,,,DOID:1923,disorder of sexual development,C0036875,,,,,
+BMGC_DS02279,BMG_DS002942,,,,,,,DOID:8541,Sezary's disease,C0036920,,,MONDO:0017844,Sezary syndrome,
+BMGC_DS02280,BMG_DS002945,,,,,,,,,C0036980,,,MONDO:0800175,cardiogenic shock,
+BMGC_DS02281,BMG_DS002946,,Short Bowel Syndrome,Short Bowel Syndrome,,,,DOID:10605,short bowel syndrome,C0036992,D012778,,MONDO:0015183,short bowel syndrome,
+BMGC_DS02282,BMG_DS002947,,Short Rib-Polydactyly Syndrome,Short Rib-Polydactyly Syndrome,,,,,,C0036996,D012779,,MONDO:0015461,short rib-polydactyly syndrome,
+BMGC_DS02283,BMG_DS002948,,Shwartzman Phenomenon,Shwartzman Phenomenon,,,,DOID:3825,Shwartzman phenomenon,C0037018,D012790,,MONDO:0002783,Shwartzman phenomenon,
+BMGC_DS02284,BMG_DS002949,,Shy-Drager Syndrome,Shy-Drager Syndrome,,,,DOID:4752,multiple system atrophy,C0037019,D012791,,,,
+BMGC_DS02285,BMG_DS002950,42982001,Sialadenitis,Sialadenitis,,,,DOID:10303,sialadenitis,C0037023,D012793,,MONDO:0006969,sialadenitis,Sialoadenitis | Sialadenitis | Sialoadenitis (disorder)
+BMGC_DS02286,BMG_DS002951,,"Sialometaplasia, Necrotizing","Sialometaplasia, Necrotizing",,,,DOID:12901,necrotizing sialometaplasia,C0037033,D012797,,MONDO:0006864,necrotizing sialometaplasia,
+BMGC_DS02287,BMG_DS002952,53827007,Sialorrhea,Sialorrhea,,,,,,C0037036,D012798,MTHU014490,,,Hypersecretion of saliva | Salivary hypersecretion | Sialorrhea | Sialosis | Hypersalivation | Polysialia | Sialism | Sialismus | Ptyalorrhea | Hypersecretion of salivary gland | Hyperactive salivary flow | Sialorrhoea | Ptyalorrhoea | Excessive salivation | Excessive salivation (disorder)
+BMGC_DS02288,BMG_DS002953,,Sick Building Syndrome,Sick Building Syndrome,,,,DOID:2710,sick building syndrome,C0037050,D018877,,MONDO:0005959,sick building syndrome,
+BMGC_DS02289,BMG_DS002954,,Sick Sinus Syndrome,Sick Sinus Syndrome,,,,DOID:13884,sick sinus syndrome,C0037052,D012804,,MONDO:0001823,sick sinus syndrome,
+BMGC_DS02290,BMG_DS002955,,Sickle Cell Trait,Sickle Cell Trait,,,,,,C0037054,D012805,,,,
+BMGC_DS02291,BMG_DS002956,155591007;266401007;62371005,Siderosis,Siderosis,CA60.8,Siderosis,J63.4,DOID:10328,siderosis,C0037061,D012806,,,,Siderosis | Pneumoconiosis NOS | (Pneumoconiosis NOS) or (siderosis) | (Pneumoconiosis NOS) or (siderosis) (disorder) | (Pneumoconiosis NOS) or (siderosis) | Pneumoconiosis NOS | Siderosis | (Pneumoconiosis NOS) or (siderosis) (disorder) | Pulmonary siderosis | Arc-welders' lung | Arc-welders' pneumoconiosis | Welders' lung | Arc-welders' disease | Welders' siderosis | Arc-welders' nodulation | Iron oxide lung | Pneumoconiosis siderotico | Siderotic lung disease | Steel grinders' disease | Iron pneumoconiosis | Siderosis | Pulmonary siderosis (disorder) | Silver polishers' lung
+BMGC_DS02292,BMG_DS002957,,Sigmoid Diseases,Sigmoid Diseases,,,,DOID:1897,sigmoid disease,C0037072,D012810,,MONDO:0002139,sigmoid disease,
+BMGC_DS02293,BMG_DS002958,,,,,,,DOID:1896,sigmoid neoplasm,C0037073,,,MONDO:0006971,sigmoid neoplasm,
+BMGC_DS02294,BMG_DS002960,805002;155590008,Silicosis,Silicosis,,,,DOID:10325,silicosis,C0037116,D012829,,MONDO:0005960,silicosis,Silicosis | Nodular silicosis | Silicatosis | Pneumoconiosis caused by silica | Pneumoconiosis caused by silica (disorder) | Silicosis | Silicosis (disorder)
+BMGC_DS02295,BMG_DS002962,,Silo Filler's Disease,Silo Filler's Disease,,,,DOID:4374,Silo filler's disease,C0037120,D012832,,MONDO:0006972,silo filler disease,
+BMGC_DS02296,BMG_DS002963,,B Virus Infection,Herpesviridae Infections,,,,,,C0037140,D006566,,MONDO:0005794,Herpesviridae infectious disease,
+BMGC_DS02297,BMG_DS002965,,Single-Gene Defects,"Genetic Diseases, Inborn",,,,,,C0037176,D030342,,,,
+BMGC_DS02298,BMG_DS002966,,Sinoatrial Block,Sinoatrial Block,,,,,,C0037188,D012848,,MONDO:0020806,sinoatrial block,
+BMGC_DS02299,BMG_DS002967,,"Sinus Thrombosis, Intracranial","Sinus Thrombosis, Intracranial",,,,DOID:3572,intracranial sinus thrombosis,C0037198,D012851,,MONDO:0002692,intracranial sinus thrombosis,
+BMGC_DS02300,BMG_DS002968,275483004;195649005;36971009,Sinusitis,Sinusitis,,,,,,C0037199,D012852,MTHU006260,MONDO:0005961,sinusitis,Sinusitis | Sinusitis (disorder) | Sinusitis (& acute) | Acute sinusitis | Sinusitis | Sinusitis (& acute) (disorder)
+BMGC_DS02301,BMG_DS002969,,,,,,,,,C0037205,,,MONDO:0017850,sirenomelia,
+BMGC_DS02302,BMG_DS002970,,,,,,,DOID:758,situs inversus,C0037221,,,,,
+BMGC_DS02303,BMG_DS002971,,Sjogren-Larsson Syndrome,Sjogren-Larsson Syndrome,,,,DOID:14501,Sjogren-Larsson syndrome,C0037231,D016111,270200,MONDO:0010031,Sjogren-Larsson syndrome,
+BMGC_DS02304,BMG_DS002973,,,,,,,DOID:37,skin disease,C0037274,,,MONDO:0005093,skin disorder,
+BMGC_DS02305,BMG_DS002974,,"Skin Diseases, Vesiculobullous","Skin Diseases, Vesiculobullous",,,,DOID:2731,vesiculobullous skin disease,C0037275,D012872,,MONDO:0006617,vesiculobullous skin disease,
+BMGC_DS02306,BMG_DS002975,,"Skin Diseases, Genetic","Skin Diseases, Genetic",,,,DOID:37,skin disease,C0037277,D012873,,MONDO:0100118, | hereditary skin disorder,
+BMGC_DS02307,BMG_DS002976,,"Skin Diseases, Infectious","Skin Diseases, Infectious",,,,,,C0037278,D012874,,MONDO:0024294;MONDO:0021201,skin disorder caused by infection | skin infection,
+BMGC_DS02308,BMG_DS002980,,,,,,,DOID:3165,skin benign neoplasm,C0037286,,,MONDO:0002531,skin neoplasm,
+BMGC_DS02309,BMG_DS002981,,,,,,,DOID:6873,skin tag,C0037293,,,MONDO:0004026,skin tag,
+BMGC_DS02310,BMG_DS002982,,Skin Ulcer,Skin Ulcer,,,,,,C0037299,D012883,,,,
+BMGC_DS02311,BMG_DS002983,,,,,,,DOID:1863,skull cancer,C0037305,,,MONDO:0024653,skull neoplasm,
+BMGC_DS02312,BMG_DS002984,,Sleep Apnea Syndromes,Sleep Apnea Syndromes,,,,DOID:0050847,sleep apnea,C0037315,D012891,,MONDO:0005296,sleep apnea syndrome,
+BMGC_DS02313,BMG_DS002986,67924001;154344005;266193008,Smallpox,Smallpox,,,B03,DOID:8736,smallpox,C0037354,D012899,,MONDO:0004651,smallpox,Smallpox | Variola | Smallpox (disorder) | Cowpox | Milker's node | Smallpox | Orf | Roseola infantum | Variola major | Other viral exanthemata | Fourth disease | Milkers' node | Fifth disease | Parascarlatina | Pseudocowpox | (Viral exanthemata [& variants]) or (orf) or (milkers node) | (Viral exanthemata [& variants]) or (orf) or (milkers node) (disorder) | Pseudocowpox | Fifth disease | Other viral exanthemata | Roseola infantum | Variola major | Cowpox | Parascarlatina | Fourth disease | Milkers' node | Milker's node | Smallpox | Orf | (Viral exanthemata [& variants]) or (orf) or (milkers node) | (Viral exanthemata [& variants]) or (orf) or (milkers node) (disorder)
+BMGC_DS02314,BMG_DS002990,,,,,,,DOID:0060123,connective tissue benign neoplasm,C0037579,,,MONDO:0006424,soft tissue neoplasm,
+BMGC_DS02315,BMG_DS002992,,,,,,,DOID:10349,solitary cyst of breast,C0037619,,,MONDO:0001009,solitary cyst of breast,
+BMGC_DS02316,BMG_DS002993,,,,,,,DOID:4737,somatoform disorder,C0037650,,,MONDO:0003117,somatoform disorder,
+BMGC_DS02317,BMG_DS002994,,,,,,,DOID:4430,somatostatinoma,C0037661,,,MONDO:0006976,somatostatinoma,
+BMGC_DS02318,BMG_DS002995,154927001;268775007;80495009,Somnambulism,Somnambulism,,,,,,C0037672,D013009,,,,Sleep disorders (& [insomnia] or [nightmares] or [sleepwalking (& somnambulism)]) | Sleep disorders | Insomnia | Nightmares | Sleepwalking | Walking in sleep | Somnambulism | Sleep disorders (& [insomnia] or [nightmares] or [sleepwalking (& somnambulism)]) (disorder) | Sleep disorders (& [insomnia] or [nightmares] or [sleepwalking (& somnambulism)]) | Nightmares | Somnambulism | Walking in sleep | Sleep disorders | Insomnia | Sleepwalking | Sleep disorders (& [insomnia] or [nightmares] or [sleepwalking (& somnambulism)]) (disorder) | Sleep walking disorder | Somnambulism | Sleep walking | Sleep walking disorder (disorder) | Sleepwalking disorder | Sleepwalking
+BMGC_DS02319,BMG_DS002996,187152002;31659000,Sparganosis,Sparganosis,1F75,Sparganosis,B70.1,DOID:10080,sparganosis,C0037753,D013031,,MONDO:0005963,sparganosis,Sparganosis | Larval dibothriocephaliasis | Larval diphyllobothriasis | Sparganosis - larval diphyllobothriasis | Sparganosis (disorder) | Infection by Spirometra larvae | Sparganosis | Larval diphyllobothriasis | Spirometriosis | Spirometrosis | Larval dibothriocephaliasis | Sparganosis - larval diphyllobothriasis | Infection caused by Spirometra larvae (disorder) | Infection caused by Spirometra larvae
+BMGC_DS02320,BMG_DS002997,,Spasmophilia,Tetany,,,,,,C0037768,D013746,,,,
+BMGC_DS02321,BMG_DS002998,,West Syndrome,"Spasms, Infantile",,,,DOID:0050562,West syndrome,C0037769,D013036,,MONDO:0018097,West syndrome,
+BMGC_DS02322,BMG_DS002999,,Spastic Paraplegia,Paraplegia,,,,,,C0037772,D010264,,,,
+BMGC_DS02323,BMG_DS003000,,"Spastic Paraplegia, Hereditary","Spastic Paraplegia, Hereditary",,,,DOID:2476,hereditary spastic paraplegia,C0037773,D015419,,MONDO:0019064,hereditary spastic paraplegia,
+BMGC_DS02324,BMG_DS003002,,Speech Disorders,Speech Disorders,,,,DOID:92,speech disorder,C0037822,D013064,,MONDO:0004730,speech disorder,
+BMGC_DS02325,BMG_DS003003,,Spermatic Cord Torsion,Spermatic Cord Torsion,,,,DOID:11996,spermatic cord torsion,C0037856,D013086,187400,MONDO:0008541,spermatic cord torsion,
+BMGC_DS02326,BMG_DS003004,155936007;49263001,Spermatocele,Spermatocele,,,,DOID:11997,spermatocele,C0037859,D013088,,MONDO:0006977,spermatocele,Spermatocele | Spermatocele (disorder) | Spermatocele | Spermatocele (disorder) | Spermatic cyst
+BMGC_DS02327,BMG_DS003005,,Sphenoid Sinusitis,Sphenoid Sinusitis,,,,DOID:10794,sphenoid sinusitis,C0037886,D015524,,MONDO:0005964,sphenoid sinusitis,
+BMGC_DS02328,BMG_DS003007,154795009;55995005,Hereditary spherocytosis,,3A10.Y,Other specified hereditary haemolytic anaemia,D58.0,DOID:12971,hereditary spherocytosis,C0037889,,,MONDO:0019350,hereditary spherocytosis,Hereditary spherocytosis | Hereditary spherocytosis (disorder) | Hereditary spherocytosis | Familial spherocytosis | Minkowsky-Chauffard syndrome | Congenital spherocytosis | Familial acholuric jaundice | Congenital spherocytic hemolytic anemia | Congenital spherocytic haemolytic anaemia | Hereditary spherocytosis (disorder) | HS - Hereditary spherocytosis
+BMGC_DS02329,BMG_DS003008,,Sphingolipidoses,Sphingolipidoses,,,,DOID:1927,sphingolipidosis,C0037899,D013106,,MONDO:0019255,sphingolipidosis,
+BMGC_DS02330,BMG_DS003009,,,,,,,,,C0037917,,,MONDO:0017069,spina bifida cystica,
+BMGC_DS02331,BMG_DS003011,71286001,Compression of spinal cord,,,,,,,C0037926,,MTHU052252,,,Spinal cord compression | Spinal cord compression (disorder) | SCC - Spinal cord compression | Compression of spinal cord
+BMGC_DS02332,BMG_DS003012,,Spinal Cord Diseases,Spinal Cord Diseases,,,,DOID:319,spinal cord disease,C0037928,D013118,,MONDO:0002545,spinal cord disorder,
+BMGC_DS02333,BMG_DS003013,,,,,,,DOID:5612,spinal cancer,C0037930,,,MONDO:0021234,spinal cord neoplasm,
+BMGC_DS02334,BMG_DS003014,,Spinal Diseases,Spinal Diseases,,,,,,C0037933,D013122,,MONDO:0000812,vertebral column disorder,
+BMGC_DS02335,BMG_DS003015,,,,,,,DOID:5612,spinal cancer,C0037939,,,,,
+BMGC_DS02336,BMG_DS003018,,Spinocerebellar Degeneration,Spinocerebellar Degenerations,,,,,,C0037952,D013132,,,,
+BMGC_DS02337,BMG_DS003020,,Splenic Diseases,Splenic Diseases,,,,DOID:2529,splenic disease,C0037997,D013158,,MONDO:0002332,splenic disorder,
+BMGC_DS02338,BMG_DS003021,,Splenic Infarction,Splenic Infarction,,,,DOID:2533,splenic infarction,C0037998,D013159,,MONDO:0006978,splenic infarction,
+BMGC_DS02339,BMG_DS003022,,,,,,,DOID:672,spleen cancer,C0037999,,,MONDO:0036696,spleen neoplasm,
+BMGC_DS02340,BMG_DS003023,84172003,Spondylitis,Spondylitis,,,,,,C0038012,D013166,,MONDO:0003937,spondylitis,Spondylitis | Spondylitis (disorder) | Spondarthritis
+BMGC_DS02341,BMG_DS003024,9631008;156619005,Ankylosing spondylitis,,,,M45,DOID:7147,ankylosing spondylitis,C0038013,,MTHU036410,MONDO:0005306,ankylosing spondylitis,Ankylosing spondylitis | Marie Strümpell spondylitis | Spondylosis deformans | Bekhterev's disease | Ankylosing spondylitis (disorder) | Marie-Strumpell spondylitis | Idiopathic ankylosing spondylitis | AS - Ankylosing spondylitis | Ankylosing spondylitis | Ankylosing spondylitis (disorder)
+BMGC_DS02342,BMG_DS003025,,Spondyloepiphyseal Dysplasia,Osteochondrodysplasias,,,,,,C0038015,D010009,,MONDO:0016761,spondyloepiphyseal dysplasia,
+BMGC_DS02343,BMG_DS003026,274152003;268349005;157003009,Spondylolisthesis,Spondylolisthesis,FA84.Z,"Spondylolisthesis, unspecified",M43.1,DOID:6682,spondylolisthesis,C0038016,D013168,184200;MTHU009825,MONDO:0008475,spondylolisthesis,"Spondylolisthesis | SPL - Spondylolisthesis | Spondylolisthesis (disorder) | (Spine anomaly - congenital) or (hemivertebra) or (Klippel-Feil syndrome) or (spina bifida occulta) or (spondylolisthesis) | Occulta - spina bifida | Spina bifida occulta | Klippel-Feil syndrome | Hemivertebra | Spondylolisthesis | Spine anomaly - congenital | Bifida, spina - occulta | (Spine anomaly - congenital) or (hemivertebra) or (Klippel-Feil syndrome) or (spina bifida occulta) or (spondylolisthesis) (disorder) | (Spine anomaly - congenital) or (hemivertebra) or (Klippel-Feil syndrome) or (spina bifida occulta) or (spondylolisthesis) | Spine anomaly - congenital | Klippel-Feil syndrome | Occulta - spina bifida | Bifida, spina - occulta | Spondylolisthesis | Hemivertebra | Spina bifida occulta | (Spine anomaly - congenital) or (hemivertebra) or (Klippel-Feil syndrome) or (spina bifida occulta) or (spondylolisthesis) (disorder)"
+BMGC_DS02344,BMG_DS003027,240221008;203688008,Spondylolysis,Spondylolysis,FA81.Z,"Spondylolysis, unspecified",M43.0,DOID:2300,spondylolysis,C0038018,D013169,MTHU036588,MONDO:0005541,spondylolysis,Spondylolysis | Spondylolysis (disorder)
+BMGC_DS02345,BMG_DS003028,8847002,Spondylosis,Spondylosis,,,M47,DOID:2247,spondylosis,C0038019,D055009,MTHU049981,MONDO:0002253,spondylosis,Spondylosis | Spondylarthrosis | Spondylosis (disorder) | Spondarthropathy
+BMGC_DS02346,BMG_DS003029,,Spondylosis Deformans,Spondylosis,,,,,,C0038020,D055009,,,,
+BMGC_DS02347,BMG_DS003031,,Spotted Fever Group Rickettsiosis,Spotted Fever Group Rickettsiosis,,,,DOID:11104,spotted fever,C0038041,D000073605,,,,
+BMGC_DS02348,BMG_DS003032,,"Sprue, Tropical","Sprue, Tropical",,,,DOID:10607,tropical sprue,C0038054,D013182,,MONDO:0001078,tropical sprue,
+BMGC_DS02349,BMG_DS003033,,,,,,,DOID:0060243,stuttering,C0038131,,,MONDO:0000723,stutter disorder,
+BMGC_DS02350,BMG_DS003034,32527003,Staphylococcal enterocolitis,,,,,,,C0038157,,,,,Staphylococcal enterocolitis | Staphylococcal enterocolitis (disorder)
+BMGC_DS02351,BMG_DS003036,,Staphylococcal Infections,Staphylococcal Infections,,,,,,C0038160,D013203,,MONDO:0024313,staphylococcal infection,
+BMGC_DS02352,BMG_DS003038,,Staphylococcal Skin Infections,Staphylococcal Skin Infections,,,,,,C0038166,D013207,,,,
+BMGC_DS02353,BMG_DS003039,,Status Asthmaticus,Status Asthmaticus,,,,DOID:9362,status asthmaticus,C0038218,D013224,,MONDO:0004766,status asthmaticus,
+BMGC_DS02354,BMG_DS003040,,Status Epilepticus,Status Epilepticus,,,,DOID:1824,status epilepticus,C0038220,D013226,,MONDO:0002125,status epilepticus,
+BMGC_DS02355,BMG_DS003042,,,,,,,,,C0038238,,,MONDO:0001075,steatorrhea,
+BMGC_DS02356,BMG_DS003044,,,,,,,DOID:2303,stereotypic movement disorder,C0038273,,,MONDO:0002265,stereotypic movement disorder,
+BMGC_DS02357,BMG_DS003045,,Stevens-Johnson Syndrome,Stevens-Johnson Syndrome,,,,DOID:0050426,Stevens-Johnson syndrome,C0038325,D013262,608579,MONDO:0018229,Stevens-Johnson syndrome,
+BMGC_DS02358,BMG_DS003046,,Gastric Dilatation,Gastric Dilatation,,,,DOID:3229,gastric dilatation,C0038353,D013271,,MONDO:0002569,gastric dilatation,
+BMGC_DS02359,BMG_DS003047,,Stomach Diseases,Stomach Diseases,,,,DOID:76,stomach disease,C0038354,D013272,,MONDO:0004298,stomach disorder,
+BMGC_DS02360,BMG_DS003048,,,,,,,DOID:10534,stomach cancer,C0038356,,,MONDO:0021085,gastric neoplasm,
+BMGC_DS02361,BMG_DS003050,397825006;196627009;6034002;155681009,Gastric ulcer,,,,K25,DOID:10808,gastric ulcer,C0038358,,,MONDO:0001126,gastric ulcer,Gastric ulcer (disorder) | Gastric ulcer | Stomach ulcer | GU - Gastric ulcer | Gastric ulceration | Gastric peptic ulcer | Peptic ulcer of stomach | Gastric ulcer (& [prepyloric] or [pyloric]) | Prepyloric ulcer | Gastric ulcer | Pyloric ulcer | Gastric ulcer - (GU) | Gastric ulcer (& [prepyloric] or [pyloric]) (disorder) | Gastric ulcer | Peptic ulcer of stomach | Stomach ulcer | GU - Gastric peptic ulcer | GU - Gastric ulcer | Gastric peptic ulcer | Gastric ulceration | Gastric ulcer (disorder) | Gastric ulcer | Gastric ulcer (disorder)
+BMGC_DS02362,BMG_DS003052,61170000;95361005,Stomatitis,Stomatitis,,,,DOID:9637,stomatitis,C0038362,D013280,MTHU008854,MONDO:0004842,stomatitis,Stomatitis | Stomatitis (disorder) | Inflammatory condition of oral mucous membrane | Inflammation of mouth | Mucous membrane inflammation | Mucitis | Mucositis | Mucosal inflammation | Inflammatory disease of mucous membrane | Inflammatory disease of mucous membrane (disorder)
+BMGC_DS02363,BMG_DS003053,,Aphthous Stomatitis,"Stomatitis, Aphthous",,,,DOID:9663,aphthous stomatitis,C0038363,D013281,,MONDO:0004845,aphthous stomatitis,
+BMGC_DS02364,BMG_DS003054,,"Stomatitis, Denture","Stomatitis, Denture",,,,DOID:11875,denture stomatitis,C0038364,D013282,,MONDO:0006723,denture stomatitis,
+BMGC_DS02365,BMG_DS003056,450005,Ulcerative stomatitis,,DA01.Z,"Disorder of oral mucosa, unspecified",K12.1,DOID:9673,ulcerative stomatitis,C0038367,,MTHU007446,MONDO:0004848,ulcerative stomatitis,Ulcerative stomatitis | Ulcerative stomatitis (disorder)
+BMGC_DS02366,BMG_DS003057,,Stomatognathic Diseases,Stomatognathic Diseases,,,,,,C0038368,D009057,,,,
+BMGC_DS02367,BMG_DS003058,22066006,Strabismus,Strabismus,,,,,,C0038379,D013285,MTHU000389,MONDO:0003432,strabismus,Strabismus | Squint | Ocular dissociation | Disorder of binocular eye movements | Strabismus (disorder)
+BMGC_DS02368,BMG_DS003059,,Streptococcal Infections,Streptococcal Infections,,,,,,C0038395,D013290,,MONDO:0021680,streptococcal infection,
+BMGC_DS02369,BMG_DS003060,,,,,,,DOID:2055,post-traumatic stress disorder,C0038436,,,MONDO:0005146,post-traumatic stress disorder,
+BMGC_DS02370,BMG_DS003061,60241006,Female stress incontinence,,,,,DOID:724,female stress incontinence,C0038437,,,MONDO:0004160,female stress incontinence,Female stress incontinence | Female urinary stress incontinence (finding) | Female urinary stress incontinence
+BMGC_DS02371,BMG_DS003062,266312006;82797006;266315008;230690007;155388006;155405006,Cerebrovascular accident,,,,,,,C0038454,,MTHU012420,MONDO:0005098,stroke disorder,Cerebrovascular: [disease] or [accident] | Cerebrovascular disease | Cerebrovascular accident | Cerebrovascular: [disease] or [accident] (disorder) | Cerebrovascular accident | Cerebrovascular accident (disorder) | Stroke NOS | Cerebrovascular accident | Stroke/CVA - undefined | Accident - cerebrovascular | Cerebral infarct | (Cerebral infarct) or (cerebrovascular accident) or (undefined stroke/CVA) or (stroke NOS) | (Cerebral infarct) or (cerebrovascular accident) or (undefined stroke/CVA) or (stroke NOS) (disorder) | CVA - Cerebrovascular accident | Stroke | Cerebrovascular accident | Cerebrovascular accident (disorder) | Cerebrovascular: [disease] or [accident] | Cerebrovascular accident | Cerebrovascular disease | Cerebrovascular: [disease] or [accident] (disorder) | Accident - cerebrovascular | Stroke NOS | Cerebral infarct | Stroke/CVA - undefined | Cerebrovascular accident | (Cerebral infarct) or (cerebrovascular accident) or (undefined stroke/CVA) or (stroke NOS) | (Cerebral infarct) or (cerebrovascular accident) or (undefined stroke/CVA) or (stroke NOS) (disorder)
+BMGC_DS02372,BMG_DS003063,,"Stromal Dystrophies, Corneal","Corneal Dystrophies, Hereditary",,,,,,C0038457,D003317,,MONDO:0020213,stromal corneal dystrophy,
+BMGC_DS02373,BMG_DS003064,,"Strongyle Infections, Equine","Strongyle Infections, Equine",,,,,,C0038459,D013319,,MONDO:0025263,"strongyle infections, equine",
+BMGC_DS02374,BMG_DS003065,1214006,Strongyloidiasis,Strongyloidiasis,,,B78,DOID:10955,strongyloidiasis,C0038463,D013322,,MONDO:0005974,strongyloidiasis,Infection by Strongyloides | Strongyloidiasis | Strongyloidosis | Infection caused by Strongyloides | Infection caused by Strongyloides (disorder)
+BMGC_DS02375,BMG_DS003067,,Sturge-Weber Syndrome,Sturge-Weber Syndrome,,,,DOID:0111563,Sturge-Weber syndrome,C0038505,D013341,185300,MONDO:0008501,Sturge-Weber syndrome,
+BMGC_DS02376,BMG_DS003068,,,,,,,DOID:0060243,stuttering,C0038506,,,,,
+BMGC_DS02377,BMG_DS003069,,Subacute Sclerosing Panencephalitis,Subacute Sclerosing Panencephalitis,,,,DOID:8970,subacute sclerosing panencephalitis,C0038522,D013344,260470,MONDO:0009835,subacute sclerosing panencephalitis,
+BMGC_DS02378,BMG_DS003070,,Subarachnoid Hemorrhage,Subarachnoid Hemorrhage,,,,,,C0038525,D013345,,MONDO:0005099,subarachnoid hemorrhage,
+BMGC_DS02379,BMG_DS003071,,Subclavian Steal Syndrome,Subclavian Steal Syndrome,,,,DOID:13002,subclavian steal syndrome,C0038531,D013349,,MONDO:0006983,subclavian steal syndrome,
+BMGC_DS02380,BMG_DS003072,,"Empyema, Subdural","Empyema, Subdural",,,,DOID:11389,subdural empyema,C0038539,D013354,,MONDO:0006984,subdural empyema,
+BMGC_DS02381,BMG_DS003074,,Submandibular Gland Diseases,Submandibular Gland Diseases,,,,DOID:12897,submandibular gland disease,C0038557,D013364,,MONDO:0001597,submandibular gland disorder,
+BMGC_DS02382,BMG_DS003081,51178009,Sudden infant death syndrome,,,,,DOID:9007,sudden infant death syndrome,C0038644,,,,,Sudden infant death syndrome | Unexpected sudden death of infant | Crib death | Cot death | Sudden infant death syndrome (finding) | SIDS - sudden infant death syndrome
+BMGC_DS02383,BMG_DS003082,32117000,Sulfhemoglobinemia,Sulfhemoglobinemia,,,,DOID:12451,sulfhemoglobinemia,C0038732,D013436,,MONDO:0006988,sulfhemoglobinemia,Sulfhemoglobinemia | Sulphaemoglobinaemia | Sulfhemoglobinemia (disorder)
+BMGC_DS02384,BMG_DS003084,192337008;48657006,Superinfection,Superinfection,,,,,,C0038826,D015163,,,,Superinfection | Superinfection (disorder) | Superimposed infection | Superimposed infection (disorder)
+BMGC_DS02385,BMG_DS003085,,Superior Mesenteric Artery Syndrome,Superior Mesenteric Artery Syndrome,,,,DOID:3557,superior mesenteric artery syndrome,C0038828,D013478,,MONDO:0002687,superior mesenteric artery syndrome,
+BMGC_DS02386,BMG_DS003086,,Superior Vena Cava Syndrome,Superior Vena Cava Syndrome,,,,,,C0038833,D013479,,MONDO:0043287,superior vena cava syndrome,
+BMGC_DS02387,BMG_DS003087,,Superior Vena Cava Thrombosis,Superior Vena Cava Syndrome,,,,,,C0038834,D013479,,,,
+BMGC_DS02388,BMG_DS003088,28978003;192975003;192976002,Progressive supranuclear palsy,,8A00.10,Progressive supranuclear palsy,G23.1,DOID:678,progressive supranuclear palsy,C0038868,,,MONDO:0019037,progressive supranuclear palsy,Progressive supranuclear ophthalmoplegia | Nuchal dystonia-dementia syndrome | Progressive supranuclear ophthalmoplegia (disorder) | Progressive supranuclear palsy | Progressive supranuclear palsy (disorder) | Progressive supranuclear palsy | Progressive supranuclear palsy (disorder) | PSP - progressive supranuclear palsy
+BMGC_DS02389,BMG_DS003089,,"Neuralgia, Supraorbital",Neuralgia,,,,,,C0038870,D009437,,,,
+BMGC_DS02390,BMG_DS003090,,,,,,,DOID:1659,supratentorial cancer,C0038874,,,,,
+BMGC_DS02391,BMG_DS003091,,,,,,,DOID:5112,copper deficiency myelopathy,C0038981,,,,,
+BMGC_DS02392,BMG_DS003092,,Sweat Gland Diseases,Sweat Gland Diseases,,,,DOID:1383,sweat gland disease,C0038986,D013543,,,,
+BMGC_DS02393,BMG_DS003093,,,,,,,DOID:2664,sweat gland benign neoplasm,C0038987,,,MONDO:0002381,sweat gland neoplasm,
+BMGC_DS02394,BMG_DS003095,,"Sweating, Gustatory","Sweating, Gustatory",,,,DOID:11599,Frey syndrome,C0038994,D013547,144100,MONDO:0007753,Frey syndrome,
+BMGC_DS02395,BMG_DS003096,,Swine Diseases,Swine Diseases,,,,,,C0039006,D013553,,MONDO:0024990,swine disease,
+BMGC_DS02396,BMG_DS003099,253005,Sycosis,Folliculitis,,,,,,C0039023,D005499,,,,Sycosis | Sycosis (disorder)
+BMGC_DS02397,BMG_DS003100,,,,,,,DOID:11193,syndactyly,C0039075,,,MONDO:0021002,syndactyly,
+BMGC_DS02398,BMG_DS003101,64572001,Syndrome,Syndrome,,,,DOID:225,syndrome,C0039082,D013577,,MONDO:0002254,syndromic disease,Disease | Clinical disease AND/OR syndrome | Disorder | Syndrome | Disorders | Diseases | Disease (disorder)
+BMGC_DS02399,BMG_DS003103,,,,,,,DOID:11971,synostosis,C0039093,,,MONDO:0001411,synostosis,
+BMGC_DS02400,BMG_DS003104,,,,,,,DOID:5485,synovial sarcoma,C0039101,,300813,MONDO:0010434,synovial sarcoma,
+BMGC_DS02401,BMG_DS003105,416209007;14107000;268092005;156666009,Synovitis,Synovitis,,,,DOID:2703,synovitis,C0039103,D013585,,MONDO:0002400,synovitis,Synovitis (disorder) | Synovitis | Synovitis | Synovitis (disorder) | Undifferentiated inflammatory arthritis | Synovitis &/or tenosynovitis | Synovitis | Synovitis/tenosynovitis | Tenosynovitis | Synovitis &/or tenosynovitis (disorder) | Synovitis/tenosynovitis | Tenosynovitis | Synovitis | Synovitis &/or tenosynovitis | Synovitis &/or tenosynovitis (disorder)
+BMGC_DS02402,BMG_DS003107,,,,,,,DOID:2702,pigmented villonodular synovitis,C0039106,,,MONDO:0024686,"tenosynovial giant cell tumor, diffuse type",
+BMGC_DS02403,BMG_DS003109,154379007;186904000;76272004,Syphilis,Syphilis,,,,,,C0039128,D013587,,MONDO:0005976,syphilis,Syphilis | Syphilis (disorder) | (Syphilis (& [other and unspecified])) or (treponemal infection) | Other and unspecified syphilis | Treponemal infection | Syphilis | (Syphilis (& [other and unspecified])) or (treponemal infection) (disorder) | Syphilis | Lues | Infection by Treponema pallidum | Treponemal infection | Treponemal disease | Luetic disease | Syphilis (disorder)
+BMGC_DS02404,BMG_DS003111,,"Syphilis, Congenital","Syphilis, Congenital",,,,DOID:9856,congenital syphilis,C0039131,D013590,,MONDO:0005714,congenital syphilis,
+BMGC_DS02405,BMG_DS003113,,"Syphilis, Latent","Syphilis, Latent",,,,DOID:9531,latent syphilis,C0039133,D013592,,MONDO:0005822,latent syphilis,
+BMGC_DS02406,BMG_DS003115,155020007;267695005;111496009,Syringomyelia,Syringomyelia,,,,DOID:327,syringomyelia,C0039144,D013595,MTHU036587,MONDO:0017987,syringomyelia,(Myelopathy NOS) or (syringomyelia) | Syringomyelia | Myelopathy NOS | (Myelopathy NOS) or (syringomyelia) (disorder) | Syringomyelia | Myelopathy NOS | (Myelopathy NOS) or (syringomyelia) | (Myelopathy NOS) or (syringomyelia) (disorder) | Syringomyelia | Hydrosyringomyelia | Syringomyelia-anesthesia syndrome | Myelosyringosis | Syringomyelia-anaesthesia syndrome | Syringomyelia (disorder)
+BMGC_DS02407,BMG_DS003117,,Tabes Dorsalis,Tabes Dorsalis,,,,DOID:10027,tabes dorsalis,C0039223,D013606,,MONDO:0005977,tabes dorsalis,
+BMGC_DS02408,BMG_DS003118,,"Tachycardia, Atrioventricular Nodal Reentry","Tachycardia, Atrioventricular Nodal Reentry",,,,,,C0039232,D013611,,,,
+BMGC_DS02409,BMG_DS003119,,"Tachycardia, Ectopic Atrial","Tachycardia, Ectopic Atrial",,,,,,C0039234,D013612,,,,
+BMGC_DS02410,BMG_DS003121,,"Tachycardia, Paroxysmal","Tachycardia, Paroxysmal",,,,,,C0039236,D013614,,,,
+BMGC_DS02411,BMG_DS003123,,Sinus Tachycardia,"Tachycardia, Sinus",,,,,,C0039239,D013616,,,,
+BMGC_DS02412,BMG_DS003124,266305002;155363003;6456007,Supraventricular tachycardia,,BC81.Z,"Supraventricular tachyarrhythmia, unspecified",I47.1,,,C0039240,,MTHU067752,,,Supraventricular tachycardia | Parox. supravent. tachycardia | Tachycardia - parox.sup | Paroxysmal atrial tachycardia | Supravent. tach. parox. | Paroxysmal artrial tachycardia | Paroxysmal sup. tachy. | Supraventricular tachycardia (& [paroxysmal] or [paroxysmal artrial]) | Supraventricular tachycardia (& [paroxysmal] or [paroxysmal artrial]) (disorder) | Supraventricular tachycardia (& [paroxysmal] or [paroxysmal artrial]) | Tachycardia - parox.sup | Paroxysmal artrial tachycardia | Paroxysmal sup. tachy. | Paroxysmal atrial tachycardia | Supravent. tach. parox. | Supraventricular tachycardia | Parox. supravent. tachycardia | Supraventricular tachycardia (& [paroxysmal] or [paroxysmal artrial]) (disorder) | Supraventricular tachycardia | Supraventricular tachycardia (disorder) | SVT - Supraventricular tachycardia
+BMGC_DS02413,BMG_DS003126,,Takayasu Arteritis,Takayasu Arteritis,,,,DOID:2508,Takayasu's arteritis,C0039263,D013625,207600,MONDO:0017991,Takayasu arteritis,
+BMGC_DS02414,BMG_DS003127,,Tangier Disease,Tangier Disease,,,,DOID:1388,Tangier disease,C0039292,D013631,205400,MONDO:0008783,Tangier disease,
+BMGC_DS02415,BMG_DS003128,,Tarsal Tunnel Syndrome,Tarsal Tunnel Syndrome,,,,DOID:12526,tarsal tunnel syndrome,C0039319,D013641,,MONDO:0006994,tarsal tunnel syndrome,
+BMGC_DS02416,BMG_DS003129,,Taste Disorders,Taste Disorders,,,,,,C0039338,D013651,,,,
+BMGC_DS02417,BMG_DS003130,,Tay-Sachs Disease,Tay-Sachs Disease,,,,DOID:3320,Tay-Sachs disease,C0039373,D013661,272800,MONDO:0010100,Tay-Sachs disease,
+BMGC_DS02418,BMG_DS003131,21877004;155449008;266324004,Hereditary hemorrhagic telangiectasia,,LA90.00,Hereditary haemorrhagic telangiectasia,I78.0,DOID:1270,hereditary hemorrhagic telangiectasia,C0039445,,,MONDO:0019180,hereditary hemorrhagic telangiectasia,Osler hemorrhagic telangiectasia syndrome | Osler-Weber-Rendu disease | Hereditary hemorrhagic telangiectasia | Osler-Rendu-Weber syndrome | Osler-Rendu-Weber disease | Osler haemorrhagic telangiectasia syndrome | Hereditary haemorrhagic telangiectasia | HHT - Hereditary haemorrhagic telangiectasia | HHT - Hereditary hemorrhagic telangiectasia | Osler hemorrhagic telangiectasia syndrome (disorder) | Telangiectasia (& [hereditary hemorrhagic]) or diseases of capillaries NOS | Diseases of capillaries NOS | Telangiectasia | Vascular spider | Telangiectasia (& [hereditary haemorrhagic]) or diseases of capillaries NOS | Heredit. hemorr.telang | Hereditary hemorrhagic telangiectasia | Hereditary haemorrhagic telangiectasia | Heredit. haemorr.telang | Telangiectasia (& [hereditary haemorrhagic]) or diseases of capillaries NOS (disorder) | Diseases of capillaries NOS | Telangiectasia | Vascular spider | Heredit. haemorr.telang | Hereditary haemorrhagic telangiectasia | Telangiectasia (& [hereditary haemorrhagic]) or diseases of capillaries NOS | Heredit. hemorr.telang | Hereditary hemorrhagic telangiectasia | Telangiectasia (& [hereditary hemorrhagic]) or diseases of capillaries NOS | Telangiectasia (& [hereditary haemorrhagic]) or diseases of capillaries NOS (disorder)
+BMGC_DS02419,BMG_DS003132,,,,,,,DOID:1272,telangiectasis,C0039446,,,MONDO:0001576,telangiectasis,
+BMGC_DS02420,BMG_DS003133,,Giant Cell Arteritis,Giant Cell Arteritis,,,,DOID:13375,temporal arteritis,C0039483,D013700,,,,
+BMGC_DS02421,BMG_DS003135,,Temporomandibular Joint Disorders,Temporomandibular Joint Disorders,,,,,,C0039494,D013705,,MONDO:0005473,temporomandibular joint disorder,
+BMGC_DS02422,BMG_DS003136,,Temporomandibular Joint Dysfunction Syndrome,Temporomandibular Joint Dysfunction Syndrome,,,,,,C0039496,D013706,,MONDO:0021895,temporomandibular joint dysfunction syndrome,
+BMGC_DS02423,BMG_DS003137,312785002;34840004,Tendinitis,Tendinopathy,,,,DOID:971,tendinitis,C0039503,D052256,,MONDO:0004857,tendinitis,Tendinitis | Tendinitis (disorder) | Tendinitis | Tendonitis | Inflammatory disorder of tendon | Tendinitis (disorder)
+BMGC_DS02424,BMG_DS003138,,Tennis Elbow,Tennis Elbow,,,,DOID:14087,epicondylitis,C0039516,D013716,,,,
+BMGC_DS02425,BMG_DS003139,240035004;67801009;156666009;268092005,Tenosynovitis,Tenosynovitis,,,,DOID:970,tenosynovitis,C0039520,D013717,MTHU007362,MONDO:0004855,tenosynovitis,Tenosynovitis | Inflammation of tendon sheath | Tenosynovitis (disorder) | Tenosynovitis | Tendinous synovitis | Tendovaginitis | Tenontolemmitis | Tenovaginitis | Inflammation of tendon sheath | Tenosynovitis (disorder) | Synovitis/tenosynovitis | Tenosynovitis | Synovitis | Synovitis &/or tenosynovitis | Synovitis &/or tenosynovitis (disorder) | Synovitis &/or tenosynovitis | Synovitis | Synovitis/tenosynovitis | Tenosynovitis | Synovitis &/or tenosynovitis (disorder)
+BMGC_DS02426,BMG_DS003140,,,,,,,DOID:3307,teratoma,C0039538,,,MONDO:0002601,teratoma,
+BMGC_DS02427,BMG_DS003141,,Testicular Diseases,Testicular Diseases,,,,DOID:2519,testicular disease,C0039584,D013733,,MONDO:0002329,testicular disorder,
+BMGC_DS02428,BMG_DS003142,,Androgen-Insensitivity Syndrome,Androgen-Insensitivity Syndrome,,,,DOID:4674,androgen insensitivity syndrome,C0039585,D013734,300068,MONDO:0019154,androgen insensitivity syndrome,
+BMGC_DS02429,BMG_DS003143,,,,,,,DOID:2998,testicular cancer,C0039590,,,MONDO:0021348,neoplasm of testis,
+BMGC_DS02430,BMG_DS003144,193607003;68216000,Tetanic cataract,,,,,DOID:13822,tetanic cataract,C0039613,,,MONDO:0001811,tetanic cataract,Tetanic cataract | Tetanic cataract (disorder) | Tetanic cataract | Tetanic cataract (disorder) | Hypocalcaemic cataract | Hypocalcemic cataract
+BMGC_DS02431,BMG_DS003145,154312006;76902006,Tetanus,Tetanus,,,,DOID:11338,tetanus,C0039614,D013742,,MONDO:0005526,tetanus,Tetanus | Tetanus (disorder)
+BMGC_DS02432,BMG_DS003146,,,,,,,DOID:6419,tetralogy of Fallot,C0039685,,187500,MONDO:0008542,tetralogy of fallot,
+BMGC_DS02433,BMG_DS003147,,Thalamic Diseases,Thalamic Diseases,,,,DOID:4662,thalamic disease,C0039726,D013786,,MONDO:0003081,thalamic disorder,
+BMGC_DS02434,BMG_DS003148,40108008;191182000;191192008;154796005;267557006,Thalassemia,Thalassemia,,,D56,DOID:10241,thalassemia,C0039730,D013789,,MONDO:0000984,thalassemia,"Thalassemia | Thalassaemia | Thalassemia (disorder) | Hereditary leptocytosis | (Thalassaemia (& Mediterranean anaemia)) or (leptocytosis, hereditary) | Mediterranean anemia | Thalassemia | Mediterranean anaemia | Thalassaemia | Leptocytosis, hereditary | (Thalassemia (& Mediterranean anemia)) or (leptocytosis, hereditary) | (Thalassaemia (& Mediterranean anaemia)) or (leptocytosis, hereditary) (disorder) | Thalassemia | Thalassaemia | Thalassaemia (disorder) | Pyruvate kinase deficiency | (Thalassemia) or (pyruvate kinase deficiency) | (Thalassaemia) or (pyruvate kinase deficiency) | Thalassaemias | Thalassaemia | Thalassemia | Thalassemias | (Thalassaemia) or (pyruvate kinase deficiency) (disorder) | (Thalassaemia) or (pyruvate kinase deficiency) | Thalassemia | Thalassemias | Thalassaemia | Thalassaemias | Pyruvate kinase deficiency | (Thalassemia) or (pyruvate kinase deficiency) | (Thalassaemia) or (pyruvate kinase deficiency) (disorder)"
+BMGC_DS02435,BMG_DS003149,,Thanatophoric Dysplasia,Thanatophoric Dysplasia,,,,DOID:13481,thanatophoric dysplasia,C0039743,D013796,,MONDO:0017042,thanatophoric dysplasia,
+BMGC_DS02436,BMG_DS003151,68771000,Theileriasis,Theileriasis,,,,DOID:3733,theileriasis,C0039753,D013801,,MONDO:0005978,theileriasis,Infection by Theileria | Theileriosis | Theileriasis | Infection caused by Theileria (disorder) | Infection caused by Theileria
+BMGC_DS02437,BMG_DS003152,,Thiamine Deficiency,Thiamine Deficiency,,,,,,C0039841,D013832,,,,
+BMGC_DS02438,BMG_DS003154,,Thoracic Diseases,Thoracic Diseases,,,,,,C0039978,D013896,,MONDO:0000651,obsolete thoracic disorder,
+BMGC_DS02439,BMG_DS003155,,,,,,,DOID:5093,thoracic cancer,C0039981,,,MONDO:0021350,neoplasm of thorax,
+BMGC_DS02440,BMG_DS003156,,Thoracic Outlet Syndrome,Thoracic Outlet Syndrome,,,,DOID:3103,thoracic outlet syndrome,C0039984,D013901,,MONDO:0005979,thoracic outlet syndrome,
+BMGC_DS02441,BMG_DS003157,32942005,Thrombasthenia,Thrombasthenia,,,,DOID:2219,Glanzmann's thrombasthenia,C0040015,D013915,273800,MONDO:0100326;MONDO:0031332,Glanzmann thrombasthenia | Glanzmann thrombasthenia 1,Hereditary thromboasthenia | Glanzmann thromboasthenia | Glanzmann-Naegeli disorder | Thrombasthenia | Glanzmann's thrombasthenia | Glanzmann's thrombasthenia (disorder) | Hereditary haemorrhagic thrombasthenia | Hereditary hemorrhagic thrombasthenia | Glanzmann's syndrome | Glanzmann's disease
+BMGC_DS02442,BMG_DS003158,,Thromboangiitis Obliterans,Thromboangiitis Obliterans,,,,DOID:12918,thromboangiitis obliterans,C0040021,D013919,211480,MONDO:0008889,thromboangiitis obliterans,
+BMGC_DS02443,BMG_DS003159,,"Thrombocythemia, Essential","Thrombocythemia, Essential",,,,DOID:2224,essential thrombocythemia,C0040028,D013920,,MONDO:0005029,essential thrombocythemia,
+BMGC_DS02444,BMG_DS003160,70786006;142969008;415116008;302215000;165556002,Thrombocytopenia,Thrombocytopenia,,,,DOID:1588,thrombocytopenia,C0040034,D013921,,MONDO:0002049,thrombocytopenia,Thrombocytopenia | Decreased platelet count | Thrombocytopenia (disorder) | Thrombocytopenia (& [auto-immune]) | Auto-immune thrombocytopenia | Thrombocytopenia | Thrombocytopenia (& [auto-immune]) (finding) | Platelet count below reference range (finding) | Platelet count below reference range | Thrombocytopenic disorder | Thrombocytopenic disorder (disorder) | Thrombocytopenia (& [auto-immune]) | Auto-immune thrombocytopenia | Thrombocytopenia | Thrombocytopenia (& [auto-immune]) (procedure)
+BMGC_DS02445,BMG_DS003161,,,,,,,DOID:3875,thrombophlebitis,C0040046,,,MONDO:0002800,thrombophlebitis,
+BMGC_DS02446,BMG_DS003162,,,,,,,,,C0040053,,,MONDO:0000831,thrombotic disease,
+BMGC_DS02447,BMG_DS003164,,,,,,,DOID:3275,thymoma,C0040100,,,MONDO:0006456,thymoma,
+BMGC_DS02448,BMG_DS003165,,Thymus Hyperplasia,Thymus Hyperplasia,,,,,,C0040115,D013952,,,,
+BMGC_DS02449,BMG_DS003167,,Thyroid Crisis,Thyroid Crisis,,,,DOID:12837,thyroid crisis,C0040127,D013958,,MONDO:0006996,thyroid crisis,
+BMGC_DS02450,BMG_DS003168,,Thyroid Diseases,Thyroid Diseases,,,,DOID:50,thyroid gland disease,C0040128,D013959,,,,
+BMGC_DS02451,BMG_DS003169,,,,,,,DOID:1781,thyroid cancer,C0040136,,,MONDO:0015074,thyroid tumor,
+BMGC_DS02452,BMG_DS003170,154664009;82119001,Thyroiditis,Thyroiditis,,,E06,DOID:7166,thyroiditis,C0040147,D013966,MTHU036938,MONDO:0004126,thyroiditis,Thyroiditis | Thyroiditis (disorder)
+BMGC_DS02453,BMG_DS003171,38727009;190296009;154666006,Subacute thyroiditis,,5A03.1,Subacute thyroiditis,E06.1,DOID:7165,subacute thyroiditis,C0040149,,,MONDO:0006982,subacute thyroiditis,Subacute thyroiditis | Pseudogranulomatous thyroiditis | Subacute thyroiditis (disorder) | Subacute thyroiditis (& [de Quervain's]) | De Quervain's thyroiditis | de Quervain's thyroiditis | De Quervain's disease | Subacute thyroiditis | Subacute thyroiditis (& [de Quervain's]) (disorder) | Subacute thyroiditis (& [de Quervain's]) | de Quervain's thyroiditis | De Quervain's disease | De Quervain's thyroiditis | Subacute thyroiditis | Subacute thyroiditis (& [de Quervain's]) (disorder)
+BMGC_DS02454,BMG_DS003172,,"Thyroiditis, Suppurative","Thyroiditis, Suppurative",,,,DOID:14350,suppurative thyroiditis,C0040150,D013969,,MONDO:0001947,suppurative thyroiditis,
+BMGC_DS02455,BMG_DS003173,154655004;190239004;267373004;90739004;267464006,Thyrotoxicosis,Thyrotoxicosis,,,,DOID:7997,thyrotoxicosis,C0040156,D013971,,MONDO:0010138,thyrotoxicosis,"Thyrotoxicosis: [+/- goitre] or [toxic goitre] or [Graves disease] or [thyroid nodule] | Thyrotoxicosis: [+/- goiter] or [toxic goiter] or [Graves disease] or [thyroid nodule] | Hyperthyroidism | Graves' disease | Nodule - thyroid, toxic | Graves disease | Thyrotoxicosis | Toxic thyroid nodule | Toxic goitre | Thyrotoxicosis +/- goitre | Goitre - toxic | Goiter - toxic | Thyrotoxicosis +/- goiter | Toxic goiter | Thyrotoxicosis: [+/- goitre] or [toxic goitre] or [Graves disease] or [thyroid nodule] (disorder) | Toxic goiter | Toxic goitre | ([Thyrotoxicosis] or [hyperthyroidism]) or (toxic goitre) | ([Thyrotoxicosis] or [hyperthyroidism]) or (toxic goiter) | Hyperthyroidism | Thyrotoxicosis | ([Thyrotoxicosis] or [hyperthyroidism]) or (toxic goitre) (disorder) | Thyrotoxicosis | Thyrotoxicosis (disorder) | Goiter - toxic | Thyrotoxicosis +/- goiter | Toxic goiter | Thyrotoxicosis: [+/- goitre] or [toxic goitre] or [Graves disease] or [thyroid nodule] | Toxic goitre | Goitre - toxic | Thyrotoxicosis +/- goitre | Toxic thyroid nodule | Thyrotoxicosis | Hyperthyroidism | Graves' disease | Nodule - thyroid, toxic | Graves disease | Thyrotoxicosis: [+/- goiter] or [toxic goiter] or [Graves disease] or [thyroid nodule] | Thyrotoxicosis: [+/- goitre] or [toxic goitre] or [Graves disease] or [thyroid nodule] (disorder)"
+BMGC_DS02456,BMG_DS003174,,,,,,,DOID:2769,tic disorder,C0040188,,,,,
+BMGC_DS02457,BMG_DS003175,,Tick Infestations,Tick Infestations,,,,DOID:4109,tick infestation,C0040196,D013984,,MONDO:0005980,tick infestation,
+BMGC_DS02458,BMG_DS003176,,Tick Paralysis,Tick Paralysis,,,,DOID:11285,tick paralysis,C0040197,D013985,,MONDO:0005981,tick paralysis,
+BMGC_DS02459,BMG_DS003179,,Tietze's Syndrome,Tietze's Syndrome,,,,DOID:14021,Tietze's syndrome,C0040213,D013991,,MONDO:0001858,Tietze syndrome,
+BMGC_DS02460,BMG_DS003180,154394006;47382004;186984003;266214005,Tinea,Tinea,,,,,,C0040247,D014005,,MONDO:0005982,tinea infection,(Dermatophytosis &/or tinea &/or ringworm) or (fungal infections) or (mycoses) | Fungal infection | Dermatophytosis | Tinea | Fungal infections | Mycoses | Ringworm | Dermatophytosis-tinea/ringworm | (Dermatophytosis &/or tinea &/or ringworm) or (fungal infections) or (mycoses) (disorder) | Dermatophytosis | Tinea | Ringworm | Microsporic tinea | Dermatophytosis (disorder) | (Dermatophytosis &/or tinea &/or ringworm) or (skin fungal infection) | Fungal infection of skin | Ringworm | Tinea | Dermatophytosis including tinea or ringworm | (Dermatophytosis &/or tinea &/or ringworm) or (skin fungal infection) (disorder) | Ringworm | Mycoses | Dermatophytosis-tinea/ringworm | Tinea | Fungal infection | Dermatophytosis | Fungal infections | (Dermatophytosis &/or tinea &/or ringworm) or (fungal infections) or (mycoses) | (Dermatophytosis &/or tinea &/or ringworm) or (fungal infections) or (mycoses) (disorder)
+BMGC_DS02461,BMG_DS003181,,White Piedra,Piedra,,,,DOID:13902,white piedra,C0040249,D010854,,MONDO:0001827,white piedra,
+BMGC_DS02462,BMG_DS003182,,Tinea Capitis,Tinea Capitis,,,,,,C0040250,D014006,,,,
+BMGC_DS02463,BMG_DS003183,84849002,Tinea corporis (disorder),,,,,,,C0040252,,,MONDO:0001461,tinea corporis,Tinea corporis | Tinea circinata | Herpes circinatus | Body tinea | Tinea corporis (disorder) | Dermatophytosis of the trunk | Tinea circinatus
+BMGC_DS02464,BMG_DS003185,,Tinea Favosa,Tinea Favosa,,,,DOID:4336,tinea favosa,C0040254,D014007,,MONDO:0005983,tinea favosa,
+BMGC_DS02465,BMG_DS003187,,Tinea Pedis,Tinea Pedis,,,,DOID:12403,tinea pedis,C0040259,D014008,,MONDO:0005984,tinea pedis,
+BMGC_DS02466,BMG_DS003188,266149008;30757001;154397004;266215006;414941008;186988000,Onychomycosis,Onychomycosis,1F28.1,Dermatophytosis of nail,B35.1,,,C0040261,D014009,MTHU041767,MONDO:0001628,tinea unguium,Dermatophytosis of nail | Tinea unguium | Dermatophytosis of nail (disorder) | Onychomycosis | Tinea of nail | Fungal infection of nail | OM - Onychomycosis | Tinea unguium | Onychomycosis | Dermatophytic onychia | Tinea of nail | Fungal infection of nail | Tinea unguium (disorder) | Onychomycosis (& [tinea of nail]) | Tinea of nail - onychomycosis | Onychomycosis | Onychomycosis (& [tinea of nail]) (disorder) | Onychomycosis (& [tinea of nail]) | Onychomycosis | Tinea of nail - onychomycosis | Onychomycosis (& [tinea of nail]) (disorder) | Onychomycosis (disorder) | Onychomycosis | Fungal infection of nail | Ringworm of nail | (Nail: [dermatophytosis] or [fungal infection]) or (onychomycosis) or (tinea unguium) | Fungal nail infection | Fungal infection of nail | Dermatophytosis of nail | Onychomycosis | Tinea unguium | (Nail: [dermatophytosis] or [fungal infection]) or (onychomycosis) or (tinea unguium) (disorder)
+BMGC_DS02467,BMG_DS003189,,Tinea Versicolor,Tinea Versicolor,,,,DOID:9060,pityriasis versicolor,C0040262,D014010,,MONDO:0005915,pityriasis versicolor,
+BMGC_DS02468,BMG_DS003190,155248003;194392000;60862001,Tinnitus,Tinnitus,MC41,Tinnitus,H93.1,,,C0040264,D014012,MTHU003968,,,Tinnitus | Tinnitus (disorder) | (Tinnitus) or (hearing noises) | Tinnitus | Hearing noises | (Tinnitus) or (hearing noises) (disorder) | Tinnitus | Noise in ears | Tinnitus (finding) | Ringing in ears
+BMGC_DS02469,BMG_DS003192,,Tolosa-Hunt Syndrome,Tolosa-Hunt Syndrome,,,,DOID:1278,tolosa-hunt syndrome,C0040381,D020333,,MONDO:0018983,Tolosa-Hunt syndrome,
+BMGC_DS02470,BMG_DS003193,,Tongue Diseases,Tongue Diseases,,,,DOID:10944,tongue disease,C0040409,D014060,,MONDO:0001165,tongue disorder,
+BMGC_DS02471,BMG_DS003194,,,,,,,,,C0040411,,,MONDO:0021240,tongue neoplasm,
+BMGC_DS02472,BMG_DS003195,,,,,,,DOID:11514,fissured tongue,C0040412,,,,,
+BMGC_DS02473,BMG_DS003196,81934005,Hairy tongue,,,,,DOID:13500,hairy tongue,C0040414,,,MONDO:0006777,hairy tongue,Black hairy tongue | Lingua villosa nigra | Melanoglossia | Black tongue | Hairy tongue | Black hairy tongue (disorder)
+BMGC_DS02474,BMG_DS003198,90176007;195665006,Tonsillitis,Tonsillitis,,,,DOID:10456,tonsillitis,C0040425,D014069,MTHU071368,,,Tonsillitis | Tonsillitis (disorder) | Tonsillitis (& acute) | Acute tonsillitis | Throat infection - tonsillitis | Tonsillitis | Tonsillitis (& acute) (disorder)
+BMGC_DS02475,BMG_DS003199,,Tooth Diseases,Tooth Diseases,,,,DOID:1091,tooth disease,C0040435,D014076,,MONDO:0006999,tooth disorder,
+BMGC_DS02476,BMG_DS003200,,Tooth Erosion,Tooth Erosion,,,,DOID:2498,tooth erosion,C0040436,D014077,,MONDO:0002325,"tooth erosion, non-bacterial",
+BMGC_DS02477,BMG_DS003202,,Tooth Resorption,Tooth Resorption,,,,DOID:13240,tooth resorption,C0040451,D014091,,MONDO:0001670,tooth resorption,
+BMGC_DS02478,BMG_DS003204,,,,,,,,,C0040457,,187100,MONDO:0008533,"teeth, supernumerary",
+BMGC_DS02479,BMG_DS003205,,Torsades de Pointes,Torsades de Pointes,,,,,,C0040479,D016171,,MONDO:0005478,torsades de pointes,
+BMGC_DS02480,BMG_DS003206,,,,,,,,,C0040485,,189600,MONDO:0008583,inherited torticollis,
+BMGC_DS02481,BMG_DS003207,192624004;268778009;5158005,Gilles de la Tourette syndrome,,,,,DOID:11119,Gilles de la Tourette syndrome,C0040517,,MTHU067724;137580,MONDO:0007661,Tourette syndrome,Gilles de la Tourette syndrome | Gilles de la Tourette syndrome (disorder) | Gilles de la Tourette syndrome | Gilles de la Tourette's syndr. | Psychogenic tics | (Psychogenic tics) or (Gilles de la Tourette's syndrome) | (Psychogenic tics) or (Gilles de la Tourette's syndrome) (disorder) | Gilles de la Tourette's syndrome | Tourette's syndrome | Tourette's disorder | Combined vocal and multiple motor tic disorder | Gilles de la Tourette's syndrome (disorder) | Gilles de la Tourette syndrome | Gilles de la Tourettes syndrome
+BMGC_DS02482,BMG_DS003208,,Toxascariasis,Toxascariasis,,,,DOID:3107,toxascariasis,C0040522,D017227,,MONDO:0005987,toxascariasis,
+BMGC_DS02483,BMG_DS003209,76695000;406619001;38995001,Toxocariasis,Toxocariasis,1F6D,Toxocariasis,B83.0,,,C0040553,D014120,,MONDO:0005988,toxocariasis,Infection by Toxascaris | Toxascariosis | Toxocariasis | Infection by Toxascaris (disorder) | Toxocara infection | Toxocariasis | Infection caused by Toxocara (disorder) | Infection caused by Toxocara | Toxocariasis | Toxocarosis | Toxocariasis (disorder)
+BMGC_DS02484,BMG_DS003210,266225001;154423006;187192000;9399000,Toxoplasmosis,Toxoplasmosis,,,B58,DOID:9965,toxoplasmosis,C0040558,D014123,,MONDO:0005989,toxoplasmosis,(Other infectious & parasitic disease) or (infestation: [leech] or [maggot]) or (myiasis) or (toxoplasmosis) | Myiasis | Toxoplasmosis | Other infectious and parasitic diseases | Maggot infestation | Leech infestation | Other infect. and parasit.dis. | (Other infectious & parasitic disease) or (infestation: [leech] or [maggot]) or (myiasis) or (toxoplasmosis) (disorder) | Maggot infestation | Myiasis | Toxoplasmosis | Leech infestation | Other infectious and parasitic diseases | Other infect. and parasit.dis. | (Other infectious & parasitic disease) or (infestation: [leech] or [maggot]) or (myiasis) or (toxoplasmosis) | (Other infectious & parasitic disease) or (infestation: [leech] or [maggot]) or (myiasis) or (toxoplasmosis) (disorder) | Toxoplasmosis | Toxoplasmosis (disorder) | Infection by Toxoplasma gondii | Infection by Toxoplasma gondii | Infection by Toxoplasma gondii (disorder)
+BMGC_DS02485,BMG_DS003212,,"Toxoplasmosis, Congenital","Toxoplasmosis, Congenital",,,,DOID:13336,congenital toxoplasmosis,C0040560,D014125,,MONDO:0005715,congenital toxoplasmosis,
+BMGC_DS02486,BMG_DS003215,,Tracheal Diseases,Tracheal Diseases,,,,DOID:3225,tracheal disease,C0040580,D014133,,,,
+BMGC_DS02487,BMG_DS003217,,Tracheal Stenosis,Tracheal Stenosis,,,,DOID:3227,tracheal stenosis,C0040583,D014135,,MONDO:0002568,tracheal stenosis,
+BMGC_DS02488,BMG_DS003218,62994001,Tracheitis,Tracheitis,,,,DOID:9392,tracheitis,C0040584,D014136,,MONDO:0005990,tracheitis,Tracheitis | Tracheitis (disorder)
+BMGC_DS02489,BMG_DS003220,57451009,Tracheobronchomegaly,Tracheobronchomegaly,,,,,,C0040587,D014137,275300,MONDO:0010148,Mounier-Kuhn syndrome,Congenital tracheobronchomegaly | Mounier-Kuhn syndrome | Tracheobronchomegaly | Congenital tracheobronchomegaly (disorder)
+BMGC_DS02490,BMG_DS003221,,,,,,,,,C0040588,,189960,MONDO:0008586,esophageal atresia/tracheoesophageal fistula,
+BMGC_DS02491,BMG_DS003222,266200005;2576002;154367007,Trachoma,Trachoma,,,A71,DOID:11265,trachoma,C0040592,D014141,,MONDO:0001249,trachoma,(AIDS with viral/chlamydial dis NOS) or (ornithosis) or (trachoma) | AIDS with viral/chlamydial disease NOS | Ornithosis | Aids +viral/chlamydial dis.NOS | Trachoma | (AIDS with viral/chlamydial dis NOS) or (ornithosis) or (trachoma) (disorder) | Trachoma | Trachoma (disorder) | (AIDS with viral/chlamydial dis NOS) or (ornithosis) or (trachoma) | Trachoma | AIDS with viral/chlamydial disease NOS | Ornithosis | Aids +viral/chlamydial dis.NOS | (AIDS with viral/chlamydial dis NOS) or (ornithosis) or (trachoma) (disorder)
+BMGC_DS02492,BMG_DS003224,,,,,,,DOID:507,adjustment disorder,C0040701,,,,,
+BMGC_DS02493,BMG_DS003225,,,,,,,DOID:2768,transient tic disorder,C0040702,,,MONDO:0002419,transient tic disorder,
+BMGC_DS02494,BMG_DS003226,,,,,,,,,C0040761,,,MONDO:0000153,transposition of the great arteries,
+BMGC_DS02495,BMG_DS003227,,,,,,,DOID:1233,transvestism,C0040774,,,,,
+BMGC_DS02496,BMG_DS003230,,Trench Fever,Trench Fever,,,,DOID:11101,trench fever,C0040830,D014205,,MONDO:0005991,trench fever,
+BMGC_DS02497,BMG_DS003233,88264003;709018004,Trichinellosis,Trichinellosis,,,B75,DOID:9784,trichinosis,C0040896,D014235,,MONDO:0019444,trichinellosis,Infection by larvae of Trichinella spiralis | Trichinosis caused by Trichinella spiralis | Trichinellosis caused by Trichinella spiralis | Trichinelliasis caused by Trichinella spiralis | Trichiniasis caused by Trichinella spiralis | Infection caused by larvae of Trichinella spiralis (disorder) | Infection caused by larvae of Trichinella spiralis | Trichinellosis | Infection by larvae of Trichinella | Trichiniasis | Trichinosis | Trichinelliasis | Infection caused by larvae of Trichinella | Infection caused by larvae of Trichinella (disorder)
+BMGC_DS02498,BMG_DS003234,,Trichomonas Infections,Trichomonas Infections,,,,DOID:1947,trichomoniasis,C0040921,D014245,,MONDO:0002154,trichomoniasis,
+BMGC_DS02499,BMG_DS003235,,Trichomonas Vaginitis,Trichomonas Vaginitis,,,,DOID:0050269,Trichomonas vaginalis trichomoniasis,C0040923,D014247,,MONDO:0005993,Trichomonas vaginitis urogenital infection,
+BMGC_DS02500,BMG_DS003239,123817002,Trichophytosis,Tinea,,,,,,C0040938,D014005,,,,Trichophytosis | Trichophytosis (disorder)
+BMGC_DS02501,BMG_DS003240,,Trichostrongyloidiasis,Trichostrongyloidiasis,,,,DOID:1255,trichostrongyloidiasis,C0040947,D014252,,MONDO:0005994,trichostrongyloidiasis,
+BMGC_DS02502,BMG_DS003241,33710003,Trichostrongylosis,Trichostrongylosis,,,,DOID:1254,trichostrongylosis,C0040948,D014253,,MONDO:0005995,trichostrongylosis,Trichostrongyliasis | Trichostrongylosis | Trichostrongyliasis (disorder) | Infection by Trichostrongylus
+BMGC_DS02503,BMG_DS003242,,,,,,,,,C0040953,,613229,MONDO:0013189,trichotillomania,
+BMGC_DS02504,BMG_DS003243,60570001,Infection by Trichuris trichiura,,,,,DOID:1252,trichuriasis,C0040954,,,,,Infection by Trichuris trichiura | Infection by Trichocephalus trichiura | Infection caused by Trichuris trichiura | Infection caused by Trichocephalus trichiura | Infection caused by Trichuris trichiura (disorder)
+BMGC_DS02505,BMG_DS003244,,Tricuspid Valve Insufficiency,Tricuspid Valve Insufficiency,,,,DOID:4080,tricuspid valve insufficiency,C0040961,D014262,,MONDO:0002870,tricuspid valve insufficiency,
+BMGC_DS02506,BMG_DS003245,,Tricuspid Valve Prolapse,Tricuspid Valve Prolapse,,,,DOID:5644,tricuspid valve prolapse,C0040962,D014263,,MONDO:0007001,tricuspid valve prolapse,
+BMGC_DS02507,BMG_DS003246,,Tricuspid Valve Stenosis,Tricuspid Valve Stenosis,,,,DOID:4078,tricuspid valve stenosis,C0040963,D014264,,MONDO:0005997,tricuspid valve stenosis,
+BMGC_DS02508,BMG_DS003247,,Trigeminal Neuralgia,Trigeminal Neuralgia,,,,DOID:12098,trigeminal neuralgia,C0040997,D014277,190400,MONDO:0008599,trigeminal neuralgia,
+BMGC_DS02509,BMG_DS003248,235108006;163644005;87866006;206809007,Trismus,Trismus,,,,,,C0041105,D014313,MTHU001188,,,Trismus | [D] Trismus | Trismus (disorder) | Trismus | Trismus (finding)
+BMGC_DS02510,BMG_DS003250,,Trombiculiasis,Trombiculiasis,,,,DOID:8399,trombiculiasis,C0041170,D014323,,MONDO:0005998,trombiculiasis,
+BMGC_DS02511,BMG_DS003251,,,,,,,DOID:4085,trophoblastic neoplasm,C0041182,,,MONDO:0002872,trophoblastic neoplasm,
+BMGC_DS02512,BMG_DS003252,65110003;186430009,Tropical pyomyositis,,FB30,Infectious myositis,M60.0,DOID:876,pyomyositis,C0041188,,,MONDO:0019168,pyomyositis,Tropical pyomyositis | Tropical myositis | Pyomyositis | Tropical pyomyositis (disorder) | Tropical pyomyositis | Tropical pyomyositis (disorder)
+BMGC_DS02513,BMG_DS003253,,,,,,,,,C0041207,,,MONDO:0018072,persistent truncus arteriosus,
+BMGC_DS02514,BMG_DS003254,266205000;154375001;78940002,Trypanosomiasis,Trypanosomiasis,,,,DOID:10113,trypanosomiasis,C0041227,D014352,,MONDO:0000940,trypanosomiasis,Trypanosomiasis | Rickettsioses etc. | Rocky Mountain spotted fever | Q fever | Typhus | Rickettsioses etc | (Rickettsioses [& named variants]) or (trypanosomiasis) | (Rickettsioses [& named variants]) or (trypanosomiasis) (disorder) | (Rickettsioses [& named variants]) or (trypanosomiasis) | Q fever | Rickettsioses etc. | Rickettsioses etc | Trypanosomiasis | Rocky Mountain spotted fever | Typhus | (Rickettsioses [& named variants]) or (trypanosomiasis) (disorder) | Trypanosomiasis | Trypanosomosis | Trypanosomiasis (disorder)
+BMGC_DS02515,BMG_DS003255,,African Trypanosomiasis,"Trypanosomiasis, African",,,,DOID:10112,sleeping sickness,C0041228,D014353,,MONDO:0005459,human African trypanosomiasis,
+BMGC_DS02516,BMG_DS003259,,Chagas Disease,Chagas Disease,,,,DOID:12140,Chagas disease,C0041234,D014355,,MONDO:0001444,Chagas disease,
+BMGC_DS02517,BMG_DS003261,15202009,Tuberculoma,Tuberculoma,,,,DOID:399,tuberculosis,C0041295,D014375,,MONDO:0021943,tuberculoma,Tuberculoma | Tuberculoma (disorder)
+BMGC_DS02518,BMG_DS003262,56717001;154281007;187285000,Tuberculosis,Tuberculosis,,,,,,C0041296,D014376,,MONDO:0018076,tuberculosis,Tuberculosis | TB - Tuberculosis | Tuberculosis (disorder) | Tuberculosis | Tuberculosis (disorder)
+BMGC_DS02519,BMG_DS003265,,"Tuberculosis, Bovine","Tuberculosis, Bovine",,,,,,C0041307,D014380,,MONDO:0025136,"tuberculosis, bovine",
+BMGC_DS02520,BMG_DS003266,,"Tuberculosis, Cardiovascular","Tuberculosis, Cardiovascular",,,,DOID:0060570,cardiac tuberculosis,C0041308,D014381,,,,
+BMGC_DS02521,BMG_DS003267,,"Tuberculosis, Cutaneous","Tuberculosis, Cutaneous",,,,,,C0041309,D014382,,MONDO:0021948,cutaneous tuberculosis,
+BMGC_DS02522,BMG_DS003270,,"Tuberculosis, Gastrointestinal","Tuberculosis, Gastrointestinal",,,,DOID:404,gastrointestinal tuberculosis,C0041312,D014385,,MONDO:0005768,gastrointestinal tuberculosis,
+BMGC_DS02523,BMG_DS003271,,"Tuberculosis, Hepatic","Tuberculosis, Hepatic",,,,DOID:407,hepatic tuberculosis,C0041313,D014386,,MONDO:0005787,hepatic tuberculosis,
+BMGC_DS02524,BMG_DS003272,,"Tuberculosis, Laryngeal","Tuberculosis, Laryngeal",,,,DOID:1583,laryngeal tuberculosis,C0041315,D014387,,MONDO:0005819,laryngeal tuberculosis,
+BMGC_DS02525,BMG_DS003275,,"Tuberculosis, Meningeal","Tuberculosis, Meningeal",,,,,,C0041318,D014390,,MONDO:0006042,meningeal tuberculosis,
+BMGC_DS02526,BMG_DS003276,,"Tuberculosis, Miliary","Tuberculosis, Miliary",,,,DOID:9861,miliary tuberculosis,C0041321,D014391,,MONDO:0005848,miliary tuberculosis,
+BMGC_DS02527,BMG_DS003277,,"Tuberculosis, Ocular","Tuberculosis, Ocular",,,,,,C0041322,D014392,,MONDO:0006876,ocular tuberculosis,
+BMGC_DS02528,BMG_DS003278,,"Tuberculosis, Oral","Tuberculosis, Oral",,,,DOID:402,oral tuberculosis,C0041323,D014393,,MONDO:0005887,oral tuberculosis,
+BMGC_DS02529,BMG_DS003280,,"Peritonitis, Tuberculous","Peritonitis, Tuberculous",,,,DOID:9801,tuberculous peritonitis,C0041325,D014395,,MONDO:0006000,tuberculous peritonitis,
+BMGC_DS02530,BMG_DS003281,,Pleural Tuberculosis,"Tuberculosis, Pleural",,,,DOID:106,pleural tuberculosis,C0041326,D014396,,MONDO:0005922,pleural tuberculosis,
+BMGC_DS02531,BMG_DS003282,,"Tuberculosis, Pulmonary","Tuberculosis, Pulmonary",,,,DOID:2957,pulmonary tuberculosis,C0041327,D014397,,MONDO:0006052,pulmonary tuberculosis,
+BMGC_DS02532,BMG_DS003283,,"Tuberculosis, Renal","Tuberculosis, Renal",,,,DOID:9733,renal tuberculosis,C0041328,D014398,,MONDO:0005938,renal tuberculosis,
+BMGC_DS02533,BMG_DS003284,,"Tuberculosis, Spinal","Tuberculosis, Spinal",,,,,,C0041330,D014399,,MONDO:0043836,"tuberculosis, spinal",
+BMGC_DS02534,BMG_DS003287,,"Tuberculosis, Urogenital","Tuberculosis, Urogenital",,,,DOID:2149,urogenital tuberculosis,C0041333,D014401,,MONDO:0006002,urogenital tuberculosis,
+BMGC_DS02535,BMG_DS003289,,,,,,,DOID:13515,tuberous sclerosis,C0041341,,,MONDO:0001734,tuberous sclerosis,
+BMGC_DS02536,BMG_DS003290,58949002,Tubo-ovarian abscess,,,,,,,C0041343,,,,,Tubo-ovarian abscess | Tubo-ovarian abscess (disorder) | Tubo ovarian abscess
+BMGC_DS02537,BMG_DS003291,,"Nephritis, Tubulointerstitial","Nephritis, Interstitial",,,,,,C0041349,D009395,,MONDO:0001085,interstitial nephritis,
+BMGC_DS02538,BMG_DS003292,19265001,Tularemia,Tularemia,,,A21,,,C0041351,D014406,,MONDO:0018077,tularemia,Tularemia | Infection by Francisella tularensis | Deer fly fever | Rabbit fever | Ohara's disease | Yatobyo | Pahvant Valley fever | Pahvant Valley plague | Tularaemia | Tularemia (disorder) | Deerfly fever | Francis' disease | O'Hara's disease
+BMGC_DS02539,BMG_DS003293,,Tumor Lysis Syndrome,Tumor Lysis Syndrome,,,,,,C0041364,D015275,,MONDO:0043875,tumor lysis syndrome,
+BMGC_DS02540,BMG_DS003294,,Turner Syndrome,Turner Syndrome,,,,DOID:3491,Turner syndrome,C0041408,D014424,,MONDO:0019499,Turner syndrome,
+BMGC_DS02541,BMG_DS003295,,"Turner Syndrome, Male",Noonan Syndrome,,,,,,C0041409,D009634,,,,
+BMGC_DS02542,BMG_DS003297,,Typhoid Fever,Typhoid Fever,,,,DOID:13258,typhoid fever,C0041466,D014435,,MONDO:0005619,typhoid fever,
+BMGC_DS02543,BMG_DS003298,,,,,,,DOID:11256,typhus,C0041471,,,MONDO:0001246,typhus,
+BMGC_DS02544,BMG_DS003299,,Endemic Flea-Borne Typhus,"Typhus, Endemic Flea-Borne",,,,DOID:11256,typhus,C0041472,D014437,,MONDO:0000330,endemic typhus,
+BMGC_DS02545,BMG_DS003300,,"Typhus, Epidemic Louse-Borne","Typhus, Epidemic Louse-Borne",,,,DOID:11256,typhus,C0041473,D014438,,MONDO:0019362,epidemic louse-borne typhus,
+BMGC_DS02546,BMG_DS003301,,,,,,,,,C0041582,,,MONDO:0043839,ulcer disease,
+BMGC_DS02547,BMG_DS003304,414490001;85807000,Infection by Uncinaria,,,,,,,C0041648,,,,,Infection by Uncinaria | Uncinariasis | Uncinariosis | Infection caused by Uncinaria | Infection caused by Uncinaria (disorder) | Infection by Uncinaria | Uncinariasis | Uncinariosis | Ancylostomiasis | Ancylostomiasis due to Ancylostoma duodenale | Ancylostomosis | Hookworm infection | Infection by Uncinaria (disorder)
+BMGC_DS02548,BMG_DS003305,,,,,,,DOID:1094,attention deficit hyperactivity disorder,C0041671,,,,,
+BMGC_DS02549,BMG_DS003306,,,,,,,DOID:1595,melancholic depression,C0041696,,,,,
+BMGC_DS02550,BMG_DS003309,,,,,,,DOID:2914,immune system disease,C0041806,,,,,
+BMGC_DS02551,BMG_DS003310,21426000,Disorder of tympanic membrane,,,,,DOID:5782,tympanic membrane disease,C0041825,,,MONDO:0003648,tympanic membrane disorder,Disorder of tympanic membrane | Disorder of tympanic membrane (disorder) | TM - Tympanic membrane disorder | Tympanic membrane disorder
+BMGC_DS02552,BMG_DS003311,247441003;70819003,Erythema,Erythema,,,,,,C0041834,D004890,MTHU015896,,,Erythema | Erythema (finding) | Erythema - observation | Erythema | Erythema (morphologic abnormality)
+BMGC_DS02553,BMG_DS003312,,,,,,,DOID:9749,internal hemorrhoid,C0041844,,,,,
+BMGC_DS02554,BMG_DS003313,,,,,,,DOID:10935,dissociative disorder,C0041857,,,,,
+BMGC_DS02555,BMG_DS003314,,,,,,,DOID:551,toxic pneumonitis,C0041881,,,,,
+BMGC_DS02556,BMG_DS003315,,Upper Respiratory Infections,Respiratory Tract Infections,,,,,,C0041912,D012141,,MONDO:0024355,respiratory tract infectious disorder,
+BMGC_DS02557,BMG_DS003316,,,,,,,,,C0041915,,,MONDO:0018844,urachal cyst,
+BMGC_DS02558,BMG_DS003317,44730006,Uremia,Uremia,,,,DOID:4676,uremia,C0041948,D014511,MTHU008842,MONDO:0007008,uremia,Uremia | Uraemia | Uremia (disorder)
+BMGC_DS02559,BMG_DS003318,95573009;31054009,Ureterolithiasis,Ureterolithiasis,,,,DOID:14146,ureterolithiasis,C0041952,D053039,,MONDO:0007009,ureterolithiasis,Ureterolithiasis | Ureterolithiasis (disorder) | Ureteric stone | Ureteral calculus | Ureteral stone | Ureteric calculus | Ureterolithiasis | Calculus of ureter | Ureteric stone (disorder)
+BMGC_DS02560,BMG_DS003319,,,,,,,DOID:11885,ureteral benign neoplasm,C0041955,,,MONDO:0021111,ureter neoplasm,
+BMGC_DS02561,BMG_DS003322,,,,,,,DOID:4022,ureterocele,C0041960,,191650,MONDO:0008628,ureterocele,
+BMGC_DS02562,BMG_DS003323,,Urethral Diseases,Urethral Diseases,,,,DOID:732,urethral disease,C0041969,D014522,,MONDO:0004184,urethral disorder,
+BMGC_DS02563,BMG_DS003324,,,,,,,DOID:730,urethral benign neoplasm,C0041971,,,MONDO:0021239,urethra neoplasm,
+BMGC_DS02564,BMG_DS003325,,Urethral Obstruction,Urethral Obstruction,,,,DOID:12577,urethral obstruction,C0041972,D014524,,MONDO:0001556,urethral obstruction,
+BMGC_DS02565,BMG_DS003326,,Urethral Stenosis,Urethral Stricture,,,,,,C0041974,D014525,,,,
+BMGC_DS02566,BMG_DS003327,31822004,Urethritis,Urethritis,,,,DOID:1343,urethritis,C0041976,D014526,,MONDO:0005297,urethritis,Urethritis | Urethritis (disorder) | Inflammation of urethra
+BMGC_DS02567,BMG_DS003328,,Urinary Stress Incontinence,"Urinary Incontinence, Stress",,,,,,C0042025,D014550,,,,
+BMGC_DS02568,BMG_DS003329,266635000;155897002;68566005,Urinary tract infection,,,,,,,C0042029,,MTHU037523,MONDO:0100338,urinary tract infection,Urinary tract infection (& [NOS]) | Urinary tract infection NOS | Infection of urinary tract | Urinary tract infection | Urinary infection NOS | Urinary tract infection (& [NOS]) (disorder) | Urinary tract infection NOS | Urinary tract infection | Urinary infection NOS | Infection of urinary tract | Urinary tract infection (& [NOS]) | Urinary tract infection (& [NOS]) (disorder) | Urinary tract infectious disease | Urinary tract infection | Urinary tract infectious disease (disorder) | UTI - Urinary tract infection
+BMGC_DS02569,BMG_DS003331,,Urination Disorders,Urination Disorders,,,,,,C0042035,D014555,,,,
+BMGC_DS02570,BMG_DS003332,,Urologic Diseases,Urologic Diseases,,,,,,C0042075,D014570,,MONDO:0002118,urinary system disorder,
+BMGC_DS02571,BMG_DS003333,,,,,,,DOID:731,urinary system benign neoplasm,C0042076,,,MONDO:0021066,urinary system neoplasm,
+BMGC_DS02572,BMG_DS003334,64305001;126485001;269433002;156427005;157756002,Urticaria,Urticaria,,,L50,,,C0042109,D014581,MTHU037793,MONDO:0005492,urticaria,Urticaria | Urticaria (morphologic abnormality) | Urticaria | Urticaria (disorder) | (Angioneurotic edema) or (urticaria) | Urticaria | Angioneurotic oedema | (Angioneurotic oedema) or (urticaria) | Angioneurotic edema | (Angioneurotic oedema) or (urticaria) (disorder) | (Angioneurotic edema) or (urticaria) | Urticaria | (Angioneurotic oedema) or (urticaria) | Angioneurotic edema | Angioneurotic oedema | (Angioneurotic oedema) or (urticaria) (disorder)
+BMGC_DS02573,BMG_DS003335,,,,,,,DOID:12309,urticaria pigmentosa,C0042111,,,MONDO:0019316,maculopapular cutaneous mastocytosis,
+BMGC_DS02574,BMG_DS003336,,Uterine Diseases,Uterine Diseases,,,,DOID:345,uterine disease,C0042131,D014591,,MONDO:0002654,uterine disorder,
+BMGC_DS02575,BMG_DS003337,,,,,,,DOID:13223,uterine fibroid,C0042133,,150699,MONDO:0007886,uterine corpus leiomyoma,
+BMGC_DS02576,BMG_DS003339,,,,,,,DOID:363,uterine cancer,C0042138,,,MONDO:0021353,tumor of uterus,
+BMGC_DS02577,BMG_DS003341,,Uveal Diseases,Uveal Diseases,,,,DOID:3480,uveal disease,C0042161,D014603,,MONDO:0002661,uveal disorder,
+BMGC_DS02578,BMG_DS003343,128473001;267719008;155116005,Uveitis,Uveitis,,,,DOID:13141,uveitis,C0042164,D014605,MTHU007399,MONDO:0020283,uveitis,Uveitis | Uveitis (disorder) | Intraocular inflammation | Cyclitis | Ciliary body disorders | Uveitis | Disorders of iris and ciliary body | Iris disorders | Iris/ciliary body disorders | Iris &/or ciliary body disorders (& [cyclitis] or [uveitis]) | Iris &/or ciliary body disorders (& [cyclitis] or [uveitis]) (disorder) | Cyclitis | Iris/ciliary body disorders | Disorders of iris and ciliary body | Ciliary body disorders | Iris disorders | Uveitis | Iris &/or ciliary body disorders (& [cyclitis] or [uveitis]) | Iris &/or ciliary body disorders (& [cyclitis] or [uveitis]) (disorder)
+BMGC_DS02579,BMG_DS003344,193500005;77971008;231946008;410692006,Anterior uveitis,,,,,DOID:1407,anterior uveitis,C0042165,,MTHU021203,MONDO:0006651,anterior uveitis,Anterior uveitis | Anterior uveitis (disorder) | Iridocyclitis | Iridocyclitis (disorder) | Anterior uveitis (disorder) | Anterior uveitis
+BMGC_DS02580,BMG_DS003345,,"Uveitis, Intermediate","Uveitis, Intermediate",,,,DOID:12732,intermediate uveitis,C0042166,D015867,,MONDO:0006806,intermediate uveitis,
+BMGC_DS02581,BMG_DS003346,,"Uveitis, Posterior","Uveitis, Posterior",,,,DOID:12574,posterior uveitis,C0042167,D015866,,MONDO:0006918,posterior uveitis,
+BMGC_DS02582,BMG_DS003347,,"Uveitis, Suppurative","Uveitis, Suppurative",,,,DOID:13140,suppurative uveitis,C0042168,D015829,,MONDO:0006990,suppurative uveitis,
+BMGC_DS02583,BMG_DS003348,,Uveomeningoencephalitic Syndrome,Uveomeningoencephalitic Syndrome,,,,DOID:12297,Vogt-Koyanagi-Harada disease,C0042170,D014607,,MONDO:0018092,Vogt-Koyanagi-Harada disease,
+BMGC_DS02584,BMG_DS003349,,Uveoparotid Fever,Uveoparotid Fever,,,,DOID:13404,uveoparotid fever,C0042171,D014608,,MONDO:0007011,uveoparotid fever,
+BMGC_DS02585,BMG_DS003351,111852003,Vaccinia,Vaccinia,,,,DOID:3298,vaccinia,C0042214,D014615,,MONDO:0002595,vaccinia,Vaccinia | Vaccinia (disorder)
+BMGC_DS02586,BMG_DS003354,,,,,,,DOID:119,vaginal cancer,C0042237,,,MONDO:0001402,vaginal cancer,
+BMGC_DS02587,BMG_DS003355,,Vaginal Diseases,Vaginal Diseases,,,,DOID:121,vaginal disease,C0042251,D014623,,MONDO:0001433,vaginal disorder,
+BMGC_DS02588,BMG_DS003356,,,,,,,DOID:119,vaginal cancer,C0042258,,,MONDO:0021050,vaginal neoplasm,
+BMGC_DS02589,BMG_DS003357,,,,,,,DOID:10131,psychologic vaginismus,C0042266,,,MONDO:0000946,psychologic vaginismus,
+BMGC_DS02590,BMG_DS003358,30800001;393596009,Vaginitis,Vaginitis,,,,DOID:2170,vaginitis,C0042267,D014627,,MONDO:0002234,vaginitis,Vaginitis | Inflammation of vagina | Vaginitis (disorder) | Vaginitis | Vaginitis (disorder)
+BMGC_DS02591,BMG_DS003359,198212006,Vaginitis and vulvovaginitis,,,,,DOID:2170,vaginitis,C0042268,,,,,Vaginitis and vulvovaginitis | Vaginitis and vulvovaginitis (disorder)
+BMGC_DS02592,BMG_DS003360,,Migraine Variant,Migraine Disorders,,,,DOID:6364,migraine,C0042331,D008881,,,,
+BMGC_DS02593,BMG_DS003361,155480003;51070004;195480007,Varicocele,Varicocele,BD75.1,Scrotal varices,I86.1,DOID:12337,varicocele,C0042341,D014646,MTHU036940,MONDO:0001498,varicocele,Varicocele | Varicocele (disorder) | Varicocele | Varicocele (disorder) | Scrotal varices
+BMGC_DS02594,BMG_DS003362,,Varicose Ulcer,Varicose Ulcer,,,,,,C0042344,D014647,,,,
+BMGC_DS02595,BMG_DS003363,,,,,,,DOID:799,varicose veins,C0042345,,192200,MONDO:0008638,varicose disease,
+BMGC_DS02596,BMG_DS003366,,,,,,,DOID:10989,conjunctival vascular disease,C0042370,,,MONDO:0001174,conjunctival vascular disorder,
+BMGC_DS02597,BMG_DS003367,,Vascular Diseases,Vascular Diseases,,,,DOID:178,vascular disease,C0042373,D014652,,MONDO:0005385,vascular disorder,
+BMGC_DS02598,BMG_DS003368,198057005,Male genital organ vascular diseases,,,,,DOID:12335,male genital organ vascular disease,C0042374,,,MONDO:0001497,male genital organ vascular disease,Male genital organ vascular diseases | Male genital organ vascular diseases (disorder)
+BMGC_DS02599,BMG_DS003369,,Vascular Headaches,Vascular Headaches,,,,,,C0042376,D014653,,MONDO:0040797,obsolete vascular headache,
+BMGC_DS02600,BMG_DS003370,195375002;393589007;31996006,Vasculitis,Vasculitis,,,,DOID:865,vasculitis,C0042384,D014657,MTHU018875,MONDO:0018882,vasculitis,Vasculitis | Vasculitis (disorder) | Vasculitis | Angiitis | Vasculitis (disorder)
+BMGC_DS02601,BMG_DS003371,,"Vasculitis, Hemorrhagic",IgA Vasculitis,,,,,,C0042386,D011695,,,,
+BMGC_DS02602,BMG_DS003374,,Velopharyngeal Insufficiency,Velopharyngeal Insufficiency,,,,,,C0042454,D014681,167500,MONDO:0008180,congenital velopharyngeal incompetence,
+BMGC_DS02603,BMG_DS003376,,Venous Insufficiency,Venous Insufficiency,,,,DOID:10128,venous insufficiency,C0042485,D014689,,MONDO:0000945,venous insufficiency,
+BMGC_DS02604,BMG_DS003377,,Ventricular Fibrillation,Ventricular Fibrillation,,,,,,C0042510,D014693,,MONDO:0000190,ventricular fibrillation,
+BMGC_DS02605,BMG_DS003378,,Ventricular Outflow Obstruction,Ventricular Outflow Obstruction,,,,,,C0042512,D014694,,,,
+BMGC_DS02606,BMG_DS003379,,"Tachycardia, Ventricular","Tachycardia, Ventricular",,,,,,C0042514,D017180,,MONDO:0005477,ventricular tachycardia,
+BMGC_DS02607,BMG_DS003380,154363006;63440008,Plantar wart,,,,B07.0,DOID:13775,plantar wart,C0042548,,,MONDO:0001795,plantar wart,Plantar wart | Plantar wart (disorder) | Verruca plantaris | Plantar wart | Verruca plantaris (disorder) | Verruca pedis | VP - verruca pedis
+BMGC_DS02608,BMG_DS003382,,Vertebral Artery Insufficiency,Vertebrobasilar Insufficiency,,,,DOID:13095,vertebral artery insufficiency,C0042560,D014715,,MONDO:0001631,vertebral artery insufficiency,
+BMGC_DS02609,BMG_DS003383,,Vertebrobasilar Insufficiency,Vertebrobasilar Insufficiency,,,,DOID:13003,vertebrobasilar insufficiency,C0042568,D014715,,MONDO:0001613,vertebrobasilar insufficiency,
+BMGC_DS02610,BMG_DS003384,,Vesico-Ureteral Reflux,Vesico-Ureteral Reflux,,,,DOID:9620,vesicoureteral reflux,C0042580,D014718,,MONDO:0006007,vesicoureteral reflux,
+BMGC_DS02611,BMG_DS003387,27001009;155935006,Seminal vesiculitis,,,,,DOID:9365,vesiculitis,C0042588,,,MONDO:0004767,vesiculitis,Seminal vesiculitis | Spermatocystitis | Seminal vesiculitis (disorder) | Seminal vesiculitis | Seminal vesiculitis (disorder)
+BMGC_DS02612,BMG_DS003388,,Vestibular Diseases,Vestibular Diseases,,,,DOID:3426,vestibular disease,C0042594,D015837,,MONDO:0002643,vestibular disorder,
+BMGC_DS02613,BMG_DS003389,,Vibrio Infections,Vibrio Infections,,,,,,C0042636,D014735,,MONDO:0007014,vibrio infectious disease,
+BMGC_DS02614,BMG_DS003390,,"Neuralgia, Vidian",Neuralgia,,,,,,C0042656,D009437,,,,
+BMGC_DS02615,BMG_DS003394,2528003,Viremia,Viremia,,,,,,C0042749,D014766,,,,Viremia | Viraemia | Viremia (finding)
+BMGC_DS02616,BMG_DS003395,,Virus Diseases,Virus Diseases,,,,DOID:934,viral infectious disease,C0042769,D014777,,MONDO:0005108,viral infectious disease | ,
+BMGC_DS02617,BMG_DS003396,,Visceral Myopathy,Intestinal Pseudo-Obstruction,,,,,,C0042781,D007418,,,,
+BMGC_DS02618,BMG_DS003398,,,,,,,,,C0042790,,,MONDO:0021084,vision disorder,
+BMGC_DS02619,BMG_DS003400,,Low Vision,"Vision, Low",,,,,,C0042798,D015354,,,,
+BMGC_DS02620,BMG_DS003401,,Vitamin A Deficiency,Vitamin A Deficiency,,,,,,C0042842,D014802,,MONDO:0007016,vitamin A deficiency,
+BMGC_DS02621,BMG_DS003402,,Vitamin B 12 Deficiency,Vitamin B 12 Deficiency,,,,DOID:0050731,vitamin B12 deficiency,C0042847,D014806,,MONDO:0020696,vitamin B12 deficiency,
+BMGC_DS02622,BMG_DS003403,,Vitamin B Deficiency,Vitamin B Deficiency,,,,,,C0042850,D014804,,MONDO:0042976,vitamin B deficiency,
+BMGC_DS02623,BMG_DS003404,,Vitamin D Deficiency,Vitamin D Deficiency,,,,,,C0042870,D014808,,MONDO:0100471,vitamin D deficiency,
+BMGC_DS02624,BMG_DS003405,,Vitamin E Deficiency,Vitamin E Deficiency,,,,,,C0042875,D014811,,,,
+BMGC_DS02625,BMG_DS003406,,Vitamin K Deficiency,Vitamin K Deficiency,,,,DOID:11249,vitamin K deficiency bleeding,C0042880,D014813,,,,
+BMGC_DS02626,BMG_DS003407,156437000;56727007,Vitiligo,Vitiligo,,,L80,DOID:12306,vitiligo,C0042900,D014820,MTHU012246,MONDO:0008661,vitiligo,Vitiligo | Vitiligo (disorder)
+BMGC_DS02627,BMG_DS003409,48142003,Vitreous abscess,,,,,DOID:9723,vitreous abscess,C0042904,,,MONDO:0004862,vitreous abscess,Vitreous abscess | Vitreous abscess (disorder)
+BMGC_DS02628,BMG_DS003410,,Vitreous Detachment,Vitreous Detachment,,,,DOID:9726,vitreous detachment,C0042907,D020255,,,,
+BMGC_DS02629,BMG_DS003413,,Voice Disorders,Voice Disorders,,,,,,C0042940,D014832,,MONDO:0043862,voice disorders,
+BMGC_DS02630,BMG_DS003414,,Volkmann Contracture,Ischemic Contracture,,,,DOID:5587,Volkmann contracture,C0042951,D054061,,MONDO:0003528,Volkmann contracture,
+BMGC_DS02631,BMG_DS003415,,Intestinal Volvulus,Intestinal Volvulus,,,,DOID:8445,intestinal volvulus,C0042961,D045822,,MONDO:0004570,intestinal volvulus,
+BMGC_DS02632,BMG_DS003416,,von Willebrand Disease,von Willebrand Diseases,,,,DOID:12531,von Willebrand's disease,C0042974,D014842,,MONDO:0024574,von Willebrand disease (hereditary or acquired),
+BMGC_DS02633,BMG_DS003418,,Vulvar Diseases,Vulvar Diseases,,,,DOID:2059,vulvar disease,C0042994,D014845,,MONDO:0002187,vulvar disease,
+BMGC_DS02634,BMG_DS003419,,,,,,,DOID:1245,vulva cancer,C0042995,,,MONDO:0021049,vulvar neoplasm,
+BMGC_DS02635,BMG_DS003420,63144007,Vulvitis,Vulvitis,,,,DOID:3901,vulvitis,C0042996,D014847,,MONDO:0007018,vulvitis,Vulvitis | Vulvitis (disorder)
+BMGC_DS02636,BMG_DS003421,53277000;266655004;155981006,Vulvovaginitis,Vulvovaginitis,,,,DOID:2273,vulvovaginitis,C0042998,D014848,MTHU026353,MONDO:0007019,vulvovaginitis,Vulvovaginitis | Vulvovaginitis (disorder) | Vulvitis - non sp. | Vulvovaginitis | Vaginitis - non sp. | Vaginitis/vulvovaginitis | Vulvo-vaginitis | Bacterial vaginosis | (Vaginitis &/or vulvovaginitis (& non specified)) or (bacterial vaginosis) or (vulvitis non specified) | (Vaginitis &/or vulvovaginitis (& non specified)) or (bacterial vaginosis) or (vulvitis non specified) (disorder) | Bacterial vaginosis | Vaginitis - non sp. | Vulvitis - non sp. | Vulvovaginitis | Vaginitis/vulvovaginitis | Vulvo-vaginitis | (Vaginitis &/or vulvovaginitis (& non specified)) or (bacterial vaginosis) or (vulvitis non specified) | (Vaginitis &/or vulvovaginitis (& non specified)) or (bacterial vaginosis) or (vulvitis non specified) (disorder)
+BMGC_DS02637,BMG_DS003422,,Lateral Medullary Syndrome,Lateral Medullary Syndrome,,,,DOID:3522,lateral medullary syndrome,C0043019,D014854,,MONDO:0006827,lateral medullary syndrome,
+BMGC_DS02638,BMG_DS003423,,,,,,,,,C0043020,,,MONDO:0043280,Wallerian degeneration,
+BMGC_DS02639,BMG_DS003424,,,,,,,DOID:11165,common wart,C0043037,,,,,
+BMGC_DS02640,BMG_DS003425,,Wasting Syndrome,Wasting Syndrome,,,,,,C0043046,D019282,,,,
+BMGC_DS02641,BMG_DS003426,,Water Intoxication,Water Intoxication,,,,,,C0043049,D014869,,MONDO:0022007,water intoxication,
+BMGC_DS02642,BMG_DS003427,,Waterhouse-Friderichsen Syndrome,Waterhouse-Friderichsen Syndrome,,,,DOID:9931,Waterhouse-Friderichsen syndrome,C0043068,D014884,,,,
+BMGC_DS02643,BMG_DS003429,,HMN (Hereditary Motor Neuropathy) Proximal Type I,Hereditary Sensory and Motor Neuropathy,,,,DOID:13137,Werdnig-Hoffmann disease,C0043116,D015417,,,,
+BMGC_DS02644,BMG_DS003430,,Werner Syndrome,Werner Syndrome,,,,DOID:5688,Werner syndrome,C0043119,D014898,277700,MONDO:0010196,Werner syndrome,
+BMGC_DS02645,BMG_DS003431,,Wernicke Encephalopathy,Wernicke Encephalopathy,,,,DOID:2384,Wernicke encephalopathy,C0043121,D014899,,MONDO:0007020,Wernicke encephalopathy,
+BMGC_DS02646,BMG_DS003432,,West Nile Fever,West Nile Fever,,,,DOID:2366,West Nile fever,C0043124,D014901,,MONDO:0002282,West Nile fever,
+BMGC_DS02647,BMG_DS003435,,Dental White Spot,Dental Caries,,,,,,C0043154,D003731,,,,
+BMGC_DS02648,BMG_DS003436,27836007,Pertussis,Whooping Cough,,,,,,C0043167,D014917,,MONDO:0005077,pertussis,Pertussis | Infection due to Bordetella pertussis | Whooping cough | WC - Whooping cough | Pertussis (disorder)
+BMGC_DS02649,BMG_DS003438,,Wiskott-Aldrich Syndrome,Wiskott-Aldrich Syndrome,,,,DOID:9169,Wiskott-Aldrich syndrome,C0043194,D014923,301000,MONDO:0010518,Wiskott-Aldrich syndrome,
+BMGC_DS02650,BMG_DS003439,,Wissler's Syndrome,Wissler's Syndrome,,,,DOID:3047,Wissler-Fanconi syndrome,C0043195,D014924,,MONDO:0006018,Wissler syndrome,
+BMGC_DS02651,BMG_DS003440,,Wolff-Parkinson-White Syndrome,Wolff-Parkinson-White Syndrome,,,,DOID:384,Wolff-Parkinson-White syndrome,C0043202,D014927,194200,MONDO:0008685,Wolff-Parkinson-White syndrome,
+BMGC_DS02652,BMG_DS003441,,Wolfram Syndrome,Wolfram Syndrome,,,,DOID:10632,Wolfram syndrome,C0043207,D014929,,MONDO:0018105,Wolfram syndrome,
+BMGC_DS02653,BMG_DS003442,,Wolman Disease,Wolman Disease,,,,DOID:14497,Wolman disease,C0043208,D015223,620151,MONDO:0019148,Wolman disease,
+BMGC_DS02654,BMG_DS003444,,,,,,,DOID:4424,juvenile xanthogranuloma,C0043324,,,MONDO:0015534,juvenile xanthogranuloma,
+BMGC_DS02655,BMG_DS003445,63103006,Xanthomatosis,Xanthomatosis,,,,DOID:3345,xanthomatosis,C0043325,D014973,,MONDO:0002615,xanthomatosis,Xanthomatosis | Xanthoma | Xanthomatosis (disorder)
+BMGC_DS02656,BMG_DS003446,52475004,Xeroderma,Ichthyosis,5B55.Y,Vitamin A deficiency with other specified manifestations,E50.8,DOID:1697,ichthyosis,C0043345,D007057,MTHU077186,,,Xeroderma | Xerodermia | Xeroderma (disorder) | Dry skin | Anhydrotic skin
+BMGC_DS02657,BMG_DS003447,,,,,,,DOID:0050427,xeroderma pigmentosum,C0043346,,,MONDO:0019600,xeroderma pigmentosum,
+BMGC_DS02658,BMG_DS003448,363677007;155167008;69316005;193887002,Xerophthalmia,Xerophthalmia,,,,DOID:10138,xerophthalmia,C0043349,D014985,MTHU057773,,,Xerophthalmia | Xerophthalmia (disorder) | Vitamin A deficiency with xerophthalmia | Vitamin A deficiency with xerophthalmia (disorder) | Conjunctival xerosis (& [xerophthalmia]) | Conjunctival xerosis | Xerophthalmia | Conjunctival xerosis (& [xerophthalmia]) (disorder)
+BMGC_DS02659,BMG_DS003449,162014002;196513007;87715008,Xerostomia,Xerostomia,DA04.6,Disturbances of salivary secretion,K11.7,,,C0043352,D014987,MTHU036698,,,Dry mouth | Xerostomia | Dry mouth (finding) | (Dry mouth) or (salivary hyposecretion) | Xerostomia | Dry mouth | Salivary hyposecretion | (Dry mouth) or (salivary hyposecretion) (disorder) | Aptyalism | Xerostomia | Absent salivary secretion | Aptyalia | Asialia | Dry mouth | Clinical xerostomia | Xerostomia (finding)
+BMGC_DS02660,BMG_DS003450,266213004;154391003;70647001,Yaws,Yaws,,,A66,DOID:10371,yaws,C0043388,D015001,,MONDO:0006019,yaws,Other venereal/spirochaete disease | Lymphogranuloma venereum | Leptospirosis | Chancroid | Yaws | Vincent's angina | Trench mouth | Angina - Vincents | Weil's disease | Spirochaete disease: [other venereal] or [Vincent's angina] or [chancroid] or [leptospirosis] or [lymphogranuloma venereum] or [trench mouth] or [Weil's disease] or [Yaws] | Spirochaete disease: [other venereal] or [Vincent's angina] or [chancroid] or [leptospirosis] or [lymphogranuloma venereum] or [trench mouth] or [Weil's disease] or [Yaws] (disorder) | Angina - Vincents | Leptospirosis | Chancroid | Weil's disease | Yaws | Vincent's angina | Trench mouth | Lymphogranuloma venereum | Spirochaete disease: [other venereal] or [Vincent's angina] or [chancroid] or [leptospirosis] or [lymphogranuloma venereum] or [trench mouth] or [Weil's disease] or [Yaws] | Other venereal/spirochaete dis | Other venereal/spirochaete disease | Spirochaete disease: [other venereal] or [Vincent's angina] or [chancroid] or [leptospirosis] or [lymphogranuloma venereum] or [trench mouth] or [Weil's disease] or [Yaws] (disorder) | Yaws | Frambesia | Pian | Buba | Infection by Treponema pertenue | Yaws (disorder) | Framboesia
+BMGC_DS02661,BMG_DS003451,,Yellow Fever,Yellow Fever,,,,DOID:9682,yellow fever,C0043395,D015004,,MONDO:0020502,yellow fever,
+BMGC_DS02662,BMG_DS003454,,Yersinia pseudotuberculosis Infections,Yersinia pseudotuberculosis Infections,,,,,,C0043410,D015012,,MONDO:0007024,Yersinia pseudotuberculosis infectious disease,
+BMGC_DS02663,BMG_DS003455,,Zellweger Syndrome,Zellweger Syndrome,,,,DOID:905,Zellweger syndrome,C0043459,D015211,,MONDO:0019609,Zellweger spectrum disorders,
+BMGC_DS02664,BMG_DS003456,267477002;154694003;53132006,Zollinger-Ellison syndrome,,5A43.Z,"Abnormal secretion of gastrin, unspecified",E16.4,DOID:0050782,Zollinger-Ellison syndrome,C0043515,,MTHU036718,MONDO:0019610,Zollinger-Ellison syndrome,Zollinger-Ellison syndr | Zollinger-Ellison syndrome | Other pancreatic secretion dis | Hyperinsulinism | Zollinger - Ellison syndrome | (Other pancreatic secretion disorder) or (hyperinsulinism) or (Zollinger-Ellison syndrome) | (Other pancreatic secretion disorder) or (hyperinsulinism) or (Zollinger-Ellison syndrome) (disorder) | Hyperinsulinism | Zollinger - Ellison syndrome | Zollinger-Ellison syndrome | Other pancreatic secretion dis | Zollinger-Ellison syndr | (Other pancreatic secretion disorder) or (hyperinsulinism) or (Zollinger-Ellison syndrome) | (Other pancreatic secretion disorder) or (hyperinsulinism) or (Zollinger-Ellison syndrome) (disorder) | Zollinger-Ellison syndrome | Zollinger-Ellison syndrome (disorder) | Excessive gastrin secretion | ZE - Zollinger-Ellison syndrome
+BMGC_DS02665,BMG_DS003458,59277005;187098003,Zygomycosis,Zygomycosis,,,B46,,,C0043541,D020096,,MONDO:0019136,Zygomycosis,Zygomycosis | Phycomycosis | Zygomycosis (disorder) | Zygomycosis (& [mucormycosis]) | Zygomycosis | Phycomycosis | Mucormycosis | Zygomycosis (& [mucormycosis]) (disorder)
+BMGC_DS02666,BMG_DS003459,,Accelerated Idioventricular Rhythm,Accelerated Idioventricular Rhythm,,,,,,C0078888,D016170,,,,
+BMGC_DS02667,BMG_DS003461,,,,,,,,,C0078917,,,MONDO:0017304,ocular albinism,
+BMGC_DS02668,BMG_DS003462,,,,,,,,,C0078918,,,MONDO:0018910,oculocutaneous albinism,
+BMGC_DS02669,BMG_DS003463,,Arachnoid Cysts,Arachnoid Cysts,,,,,,C0078981,D016080,,MONDO:0008813,arachnoid cyst,
+BMGC_DS02670,BMG_DS003465,,Cerebral Thrombosis,Intracranial Thrombosis,,,,DOID:4193,intracranial thrombosis,C0079102,D020767,,,,
+BMGC_DS02671,BMG_DS003466,,Cockayne-Touraine Disease,Epidermolysis Bullosa Dystrophica,,,,,,C0079136,D016108,,,,
+BMGC_DS02672,BMG_DS003467,,"Hyperkeratosis, Epidermolytic","Hyperkeratosis, Epidermolytic",,,,DOID:4603,epidermolytic hyperkeratosis,C0079153,D017488,,MONDO:0007239,epidermolytic ichthyosis,
+BMGC_DS02673,BMG_DS003468,,Congenital Nonbullous Ichthyosiform Erythroderma,"Ichthyosis, Lamellar",,,,DOID:0060655,autosomal recessive congenital ichthyosis,C0079154,D017490,,MONDO:0019306,congenital non-bullous ichthyosiform erythroderma,
+BMGC_DS02674,BMG_DS003470,,,,,,,,,C0079218,,135290,MONDO:0007608,desmoid tumor,
+BMGC_DS02675,BMG_DS003472,,Epidermolysis Bullosa Acquisita,Epidermolysis Bullosa Acquisita,,,,DOID:4313,epidermolysis bullosa acquisita,C0079293,D016107,,MONDO:0018747,acquired epidermolysis bullosa,
+BMGC_DS02676,BMG_DS003473,,Epidermolysis Bullosa Dystrophica,Epidermolysis Bullosa Dystrophica,,,,DOID:4959,epidermolysis bullosa dystrophica,C0079294,D016108,,MONDO:0006543,epidermolysis bullosa dystrophica,
+BMGC_DS02677,BMG_DS003474,,Epidermolysis Bullosa Herpetiformis Dowling-Meara,Epidermolysis Bullosa Simplex,,,,,,C0079295,D016110,131760,MONDO:0007550,"epidermolysis bullosa simplex 1A, generalized severe",
+BMGC_DS02678,BMG_DS003475,,Epidermolysis Bullosa Progressiva,"Epidermolysis Bullosa, Junctional",,,,,,C0079297,D016109,,,,
+BMGC_DS02679,BMG_DS003476,,Epidermolysis Bullosa Simplex,Epidermolysis Bullosa Simplex,,,,DOID:4644,epidermolysis bullosa simplex,C0079298,D016110,,MONDO:0017610,epidermolysis bullosa simplex,
+BMGC_DS02680,BMG_DS003477,,Junctional Epidermolysis Bullosa,"Epidermolysis Bullosa, Junctional",,,,DOID:3209,junctional epidermolysis bullosa,C0079301,D016109,,MONDO:0017612,junctional epidermolysis bullosa,
+BMGC_DS02681,BMG_DS003479,,Hallopeau-Siemens Disease,Epidermolysis Bullosa Dystrophica,,,,,,C0079474,D016108,226600,MONDO:0009179,recessive dystrophic epidermolysis bullosa,
+BMGC_DS02682,BMG_DS003480,,Heart Valve Prolapse,Heart Valve Prolapse,,,,DOID:4079,heart valve disease,C0079485,D016127,,,,
+BMGC_DS02683,BMG_DS003481,,Helicobacter Infections,Helicobacter Infections,,,,,,C0079487,D016481,,MONDO:0006781,Helicobacter pylori infectious disease,
+BMGC_DS02684,BMG_DS003482,,Hermanski-Pudlak Syndrome,Hermanski-Pudlak Syndrome,,,,DOID:3753,Hermansky-Pudlak syndrome,C0079504,D022861,,MONDO:0019312,Hermansky-Pudlak syndrome,
+BMGC_DS02685,BMG_DS003483,,,,,,,DOID:4621,holoprosencephaly,C0079541,,,MONDO:0016296,holoprosencephaly,
+BMGC_DS02686,BMG_DS003484,,"Ichthyosiform Erythroderma, Congenital","Ichthyosiform Erythroderma, Congenital",,,,,,C0079583,D016113,,,,
+BMGC_DS02687,BMG_DS003485,,Ichthyosis Vulgaris,Ichthyosis Vulgaris,,,,DOID:1702,ichthyosis vulgaris,C0079584,D016112,,MONDO:0024304,ichthyosis vulgaris,
+BMGC_DS02688,BMG_DS003486,,"Ichthyosis, X-Linked","Ichthyosis, X-Linked",,,,DOID:1700,X-linked ichthyosis,C0079588,D016114,308100,MONDO:0010622,recessive X-linked ichthyosis,
+BMGC_DS02689,BMG_DS003487,,Klein's Syndrome,Waardenburg Syndrome,,,,DOID:9258,Waardenburg syndrome,C0079661,D014849,148820,MONDO:0007862,Waardenburg syndrome type 3,
+BMGC_DS02690,BMG_DS003488,,Lentivirus Infections,Lentivirus Infections,,,,,,C0079680,D016180,,MONDO:0022034,lentivirus infection,
+BMGC_DS02691,BMG_DS003489,,Herlitz Disease,"Epidermolysis Bullosa, Junctional",,,,,,C0079683,D016109,226700,MONDO:0009182,junctional epidermolysis bullosa Herlitz type,
+BMGC_DS02692,BMG_DS003490,,,,,,,DOID:707,B-cell lymphoma,C0079731,,,MONDO:0004095,B-cell neoplasm,
+BMGC_DS02693,BMG_DS003491,,,,,,,,,C0079744,,,MONDO:0018905,diffuse large B-cell lymphoma,
+BMGC_DS02694,BMG_DS003494,,,,,,,DOID:0081312,T-cell non-Hodgkin lymphoma,C0079772,,,MONDO:0015760,T-cell non-Hodgkin lymphoma,
+BMGC_DS02695,BMG_DS003495,,,,,,,,,C0079773,,,MONDO:0015758,primary cutaneous T-cell lymphoma,
+BMGC_DS02696,BMG_DS003496,,,,,,,,,C0079774,,,MONDO:0019476,primary cutaneous peripheral T-cell lymphoma not otherwise specified,
+BMGC_DS02697,BMG_DS003497,,,,,,,DOID:4376,milk allergy,C0079840,,,,,
+BMGC_DS02698,BMG_DS003498,,,,,,,DOID:12215,oligohydramnios,C0079924,,,MONDO:0005881,oligohydramnios,
+BMGC_DS02699,BMG_DS003502,,,,,,,DOID:3263,piebaldism,C0080024,,172800,MONDO:0008244,piebaldism,
+BMGC_DS02700,BMG_DS003504,,Postpoliomyelitis Syndrome,Postpoliomyelitis Syndrome,,,,DOID:4952,postpoliomyelitis syndrome,C0080040,D016262,,MONDO:0017416,postpoliomyelitis syndrome,
+BMGC_DS02701,BMG_DS003506,,Vesicular Skin Diseases,"Skin Diseases, Vesiculobullous",,,,,,C0080159,D012872,,,,
+BMGC_DS02702,BMG_DS003508,,,,,,,DOID:0080016,spina bifida,C0080178,,,MONDO:0008449,spina bifida,
+BMGC_DS02703,BMG_DS003509,,Tethered Cord Syndrome,Neural Tube Defects,,,,,,C0080218,D009436,,MONDO:0006995,tethered spinal cord syndrome,
+BMGC_DS02704,BMG_DS003512,,Weber-Cockayne Syndrome,Epidermolysis Bullosa Simplex,,,,,,C0080333,D016110,131800,MONDO:0007551,"epidermolysis bullosa simplex 1C, localized",
+BMGC_DS02705,BMG_DS003514,,Granuloma Annulare,Granuloma Annulare,,,,DOID:3777,granuloma annulare,C0085074,D016460,,MONDO:0006554,granuloma annulare,
+BMGC_DS02706,BMG_DS003515,,Sweet Syndrome,Sweet Syndrome,,,,DOID:0080746,Sweet syndrome,C0085077,D016463,608068,MONDO:0011959,sweet syndrome,
+BMGC_DS02707,BMG_DS003516,,Lysosomal Storage Diseases,Lysosomal Storage Diseases,,,,DOID:3211,lysosomal storage disease,C0085078,D016464,,MONDO:0002561,lysosomal storage disease,
+BMGC_DS02708,BMG_DS003517,240695000;399314004;434532004;57202009,Fungemia,Fungemia,,,,,,C0085082,D016469,,,,Fungemia | Fungaemia | Fungaemia (disorder) | Systemic mycosis (disorder) | Systemic mycosis | Systemic fungal infection | Disseminated mycosis | Fungemia (finding) | Fungaemia | Fungemia | Systemic mycosis | Systemic fungal infection | Fungemia | Disseminated hyalohyphomycosis | Disseminated mycosis | Fungaemia | Systemic mycosis (disorder)
+BMGC_DS02709,BMG_DS003518,,Ovarian Hyperstimulation Syndrome,Ovarian Hyperstimulation Syndrome,,,,DOID:5425,ovarian hyperstimulation syndrome,C0085083,D016471,608115,MONDO:0011972,ovarian hyperstimulation syndrome,
+BMGC_DS02710,BMG_DS003519,,Motor Neuron Disease,Motor Neuron Disease,,,,DOID:231,motor neuron disease,C0085084,D016472,,MONDO:0020128,motor neuron disorder,
+BMGC_DS02711,BMG_DS003520,,Peripheral Vascular Diseases,Peripheral Vascular Diseases,,,,,,C0085096,D016491,,MONDO:0005294,peripheral vascular disease,
+BMGC_DS02712,BMG_DS003521,79468000,Familial benign pemphigus,,,,,DOID:0050429,Hailey-Hailey disease,C0085106,,169600,MONDO:0008218,Hailey-Hailey disease,Familial benign pemphigus | Hailey-Hailey disease | Familial benign chronic pemphigus | Familial benign pemphigus (disorder) | Benign familial chronic pemphigus | Hailey Hailey disease
+BMGC_DS02713,BMG_DS003522,,Corneal Neovascularization,Corneal Neovascularization,,,,DOID:11382,corneal neovascularization,C0085109,D016510,,MONDO:0006713,corneal neovascularization,
+BMGC_DS02714,BMG_DS003523,,Severe Combined Immunodeficiency,Severe Combined Immunodeficiency,,,,DOID:627,severe combined immunodeficiency,C0085110,D016511,,MONDO:0015974,severe combined immunodeficiency,
+BMGC_DS02715,BMG_DS003524,,Foot Ulcer,Foot Ulcer,,,,,,C0085119,D016523,,,,
+BMGC_DS02716,BMG_DS003525,,Bronchial Hyperreactivity,Bronchial Hyperreactivity,,,,,,C0085129,D016535,,,,
+BMGC_DS02717,BMG_DS003526,,Gangliosidosis GM1,"Gangliosidosis, GM1",,,,DOID:3322,GM1 gangliosidosis,C0085131,D016537,,MONDO:0018149,GM1 gangliosidosis,
+BMGC_DS02718,BMG_DS003527,,Mucopolysaccharidosis VII,Mucopolysaccharidosis VII,,,,DOID:12803,Sly syndrome,C0085132,D016538,253220,MONDO:0009662,mucopolysaccharidosis type 7,
+BMGC_DS02719,BMG_DS003528,,,,,,,DOID:3620,central nervous system cancer,C0085136,,,MONDO:0006130,central nervous system neoplasm,
+BMGC_DS02720,BMG_DS003529,,,,,,,DOID:3540,choroid plexus cancer,C0085138,,,MONDO:0016717,choroid plexus neoplasm,
+BMGC_DS02721,BMG_DS003530,,,,,,,,,C0085159,,,MONDO:0000694,seasonal affective disorder,
+BMGC_DS02722,BMG_DS003531,267814008;201204008;267866004;156417004;69741000,Hidradenitis,Hidradenitis,,,,DOID:2282,hidradenitis,C0085160,D016575,,MONDO:0002260,hidradenitis,Hidradenitis | Hidradenitis (disorder) | Hidradenitis (& hidradenitis suppurativa) | Hidradenitis | Hidradenitis suppurativa | Hidradenitis (& hidradenitis suppurativa) (disorder) | Hidradenitis | Hydradenitis | Dyshidrosis | Hidradenitis suppurativa | Sweat gland problems NOS | (Sweat gland problems NOS) or (dyshidrosis) or (hydradenitis (& [suppurativa]) | (Sweat gland problems NOS) or (dyshidrosis) or (hydradenitis (& [suppurativa]) (disorder) | Sweat gland problems NOS | Hidradenitis suppurativa | Hydradenitis | Dyshidrosis | Hidradenitis | (Sweat gland problems NOS) or (dyshidrosis) or (hydradenitis (& [suppurativa]) | (Sweat gland problems NOS) or (dyshidrosis) or (hydradenitis (& [suppurativa]) (disorder)
+BMGC_DS02723,BMG_DS003532,,Bacterial Vaginosis,"Vaginosis, Bacterial",,,,DOID:3385,bacterial vaginosis,C0085166,D016585,,MONDO:0005316,bacterial vaginosis,
+BMGC_DS02724,BMG_DS003533,,,,,,,DOID:2411,granular cell tumor,C0085167,,,MONDO:0006235,granular cell tumor,
+BMGC_DS02725,BMG_DS003534,,Eosinophilia-Myalgia Syndrome,Eosinophilia-Myalgia Syndrome,,,,DOID:998,eosinophilia-myalgia syndrome,C0085179,D016603,,MONDO:0004941,eosinophilia-myalgia syndrome,
+BMGC_DS02726,BMG_DS003535,,Gestational Diabetes,"Diabetes, Gestational",,,,DOID:11714,gestational diabetes,C0085207,D016640,,MONDO:0005406,gestational diabetes,
+BMGC_DS02727,BMG_DS003536,,"Encephalopathy, Bovine Spongiform","Encephalopathy, Bovine Spongiform",,,,DOID:5435,variant Creutzfeldt-Jakob disease,C0085209,D016643,,MONDO:0025149,"encephalopathy, bovine spongiform",
+BMGC_DS02728,BMG_DS003537,,"Ovarian Failure, Premature",Primary Ovarian Insufficiency,,,,DOID:5426,primary ovarian insufficiency,C0085215,D016649,,MONDO:0005387,primary ovarian failure,
+BMGC_DS02729,BMG_DS003538,,Cerebral Amyloid Angiopathy,Cerebral Amyloid Angiopathy,,,,,,C0085220,D016657,,,,
+BMGC_DS02730,BMG_DS003539,,Psoas Abscess,Psoas Abscess,,,,,,C0085222,D016659,,,,
+BMGC_DS02731,BMG_DS003541,,Adult-Onset Still Disease,"Still's Disease, Adult-Onset",,,,DOID:14256,adult-onset Still's disease,C0085253,D016706,,MONDO:0019355,adult-onset Still disease,
+BMGC_DS02732,BMG_DS003542,,,,,,,DOID:13482,Proteus syndrome,C0085261,,176920,MONDO:0008318,Proteus syndrome,
+BMGC_DS02733,BMG_DS003543,,,,,,,DOID:3677,pulmonary plasma cell granuloma,C0085269,,,MONDO:0006933,pulmonary plasma cell granuloma,
+BMGC_DS02734,BMG_DS003544,,Orbital Pseudotumor,Orbital Pseudotumor,,,,DOID:9369,orbital plasma cell granuloma,C0085270,D016727,,MONDO:0004769,orbital pseudotumor,
+BMGC_DS02735,BMG_DS003545,,Erythema Infectiosum,Erythema Infectiosum,,,,DOID:8743,erythema infectiosum,C0085273,D016731,,MONDO:0006544,erythema infectiosum,
+BMGC_DS02736,BMG_DS003547,,Antiphospholipid Syndrome,Antiphospholipid Syndrome,,,,DOID:2988,antiphospholipid syndrome,C0085278,D016736,,MONDO:8000010,antiphospholipid syndrome,
+BMGC_DS02737,BMG_DS003548,,,,,,,DOID:9245,Alagille syndrome,C0085280,,,MONDO:0007318,Alagille syndrome,
+BMGC_DS02738,BMG_DS003549,,Stiff-Person Syndrome,Stiff-Person Syndrome,,,,DOID:13366,Stiff-Person syndrome,C0085292,D016750,184850,MONDO:0008491,stiff-person syndrome,
+BMGC_DS02739,BMG_DS003550,7111000119109,Hepatitis E,Hepatitis E,,,,DOID:4411,hepatitis E,C0085293,D016751,,MONDO:0005788,hepatitis E virus infection,Hepatitis E virus infection | Viral hepatitis E | Viral hepatitis type E (disorder) | Viral hepatitis type E | Hepatitis E
+BMGC_DS02740,BMG_DS003552,,Embolism and Thrombosis,Embolism and Thrombosis,,,,,,C0085307,D016769,,,,
+BMGC_DS02741,BMG_DS003553,,Ciliophora Infections,Ciliophora Infections,,,,,,C0085308,D016770,,MONDO:0005704,Ciliophora infectious disease,
+BMGC_DS02742,BMG_DS003556,,"Toxoplasmosis, Cerebral","Toxoplasmosis, Cerebral",,,,,,C0085315,D016781,,MONDO:0005697,cerebral toxoplasmosis,
+BMGC_DS02743,BMG_DS003559,,Li-Fraumeni Syndrome,Li-Fraumeni Syndrome,,,,DOID:3012,Li-Fraumeni syndrome,C0085390,D016864,609266;151623,MONDO:0018875,Li-Fraumeni syndrome,
+BMGC_DS02744,BMG_DS003561,,Serratia Infections,Serratia Infections,,,,,,C0085394,D016868,,,,
+BMGC_DS02745,BMG_DS003563,,Neisseriaceae Infections,Neisseriaceae Infections,,,,,,C0085396,D016870,,,,
+BMGC_DS02746,BMG_DS003564,,Pasteurellaceae Infections,Pasteurellaceae Infections,,,,,,C0085397,D016871,,,,
+BMGC_DS02747,BMG_DS003565,77361002,Ehrlichiosis,Ehrlichiosis,,,A77.4,DOID:10242,ehrlichiosis,C0085399,D016873,,MONDO:0016003,ehrlichiosis,Ehrlichiosis | Ehrlichiosis (disorder)
+BMGC_DS02748,BMG_DS003566,,POEMS Syndrome,POEMS Syndrome,,,,DOID:14039,POEMS syndrome,C0085404,D016878,,MONDO:0017364,POEMS syndrome,
+BMGC_DS02749,BMG_DS003567,699676006;61842000,Microsporidiosis,Microsporidiosis,1F5Z,Unspecified protozoal disease,B60.8,DOID:4271,microsporidiosis,C0085407,D016881,,MONDO:0005846,microsporidiosis,Infection by Microsporidia | Microsporidiosis | Infection caused by Microsporidia | Infection caused by Microsporidia (disorder) | Infection by Microsporida | Infection by Microsporidia | Infection by Cnidosporidia | Microsporidiosis | Microsporidiasis | Infection by Microsporida (disorder)
+BMGC_DS02750,BMG_DS003568,,"Polyendocrinopathies, Autoimmune","Polyendocrinopathies, Autoimmune",,,,DOID:14040,autoimmune polyendocrine syndrome,C0085409,D016884,,MONDO:0017278,autoimmune polyendocrinopathy,
+BMGC_DS02751,BMG_DS003569,71072006,Angiodysplasia,Angiodysplasia,,,,DOID:2494,angiodysplasia,C0085411,D016888,MTHU006470,MONDO:0002322,angiodysplasia,Angiodysplasia | Angiodysplasia (morphologic abnormality)
+BMGC_DS02752,BMG_DS003570,12825006,Encephalitozoonosis,Encephalitozoonosis,,,,DOID:4270,encephalitozoonosis,C0085412,D016890,,MONDO:0005743,encephalitozoonosis,Infection by Encephalitozoon | Encephalitozoonosis | Infection caused by Encephalitozoon (disorder) | Infection caused by Encephalitozoon
+BMGC_DS02753,BMG_DS003571,,"Polycystic Kidney, Autosomal Dominant","Polycystic Kidney, Autosomal Dominant",,,,,,C0085413,D016891,,MONDO:0004691,autosomal dominant polycystic kidney disease,
+BMGC_DS02754,BMG_DS003572,,"Epilepsy, Complex Partial","Epilepsy, Complex Partial",,,,DOID:12382,complex partial epilepsy,C0085417,D017029,,MONDO:0006710,complex partial epilepsy,
+BMGC_DS02755,BMG_DS003573,,Gram-Negative Bacterial Infections,Gram-Negative Bacterial Infections,,,,,,C0085423,D016905,,MONDO:0021678,gram-negative bacterial infections,
+BMGC_DS02756,BMG_DS003574,,Gram-Positive Bacterial Infections,Gram-Positive Bacterial Infections,,,,,,C0085426,D016908,,MONDO:0021679,gram-positive bacterial infections,
+BMGC_DS02757,BMG_DS003575,,"Angiomatosis, Bacillary","Angiomatosis, Bacillary",,,,DOID:0060345,bacillary angiomatosis,C0085434,D016917,,MONDO:0000758,bacillary angiomatosis,
+BMGC_DS02758,BMG_DS003576,,"Arthritis, Reactive","Arthritis, Reactive",,,,,,C0085435,D016918,,MONDO:0017376,reactive arthritis,
+BMGC_DS02759,BMG_DS003577,,"Meningitis, Cryptococcal","Meningitis, Cryptococcal",,,,DOID:0080159,Cryptococcal meningitis,C0085436,D016919,,MONDO:0005723,Cryptococcal meningitis,
+BMGC_DS02760,BMG_DS003578,,"Meningitis, Bacterial","Meningitis, Bacterial",,,,DOID:9470,bacterial meningitis,C0085437,D016920,,MONDO:0006670,bacterial meningitis,
+BMGC_DS02761,BMG_DS003579,,"Meningitis, Fungal","Meningitis, Fungal",,,,DOID:11608,fungal meningitis,C0085438,D016921,,MONDO:0006764,fungal meningitis,
+BMGC_DS02762,BMG_DS003581,,"Epilepsy, Frontal Lobe","Epilepsy, Frontal Lobe",,,,DOID:3331,frontal lobe epilepsy,C0085541,D017034,,MONDO:0002612,frontal lobe epilepsy,
+BMGC_DS02763,BMG_DS003583,,"Phenylketonuria, Maternal","Phenylketonuria, Maternal",,,,DOID:9281,phenylketonuria,C0085547,D017042,,MONDO:0016366,maternal phenylketonuria,
+BMGC_DS02764,BMG_DS003584,,Autosomal Recessive Polycystic Kidney Disease,"Polycystic Kidney, Autosomal Recessive",,,,DOID:0110861,autosomal recessive polycystic kidney disease,C0085548,D017044,,MONDO:0009889,autosomal recessive polycystic kidney disease,
+BMGC_DS02765,BMG_DS003585,,Buruli Ulcer,Buruli Ulcer,,,,DOID:0050456,Buruli ulcer disease,C0085568,D054312,,MONDO:0000327,Buruli ulcer disease,
+BMGC_DS02766,BMG_DS003586,18104000,"Metabolic acidosis, NAG, acidifying salts",,,,,,,C0085569,,,,,"Metabolic acidosis, NAG, acidifying salts | Hyperchloremic acidosis | Hyperchloraemic acidosis | Metabolic acidosis, normal anion gap, acidifying salts | Metabolic acidosis, normal anion gap, acidifying salts (disorder)"
+BMGC_DS02767,BMG_DS003588,202455001;50442003,Palindromic rheumatism,,FA27.2,Palindromic rheumatism,M12.3,DOID:1166,palindromic rheumatism,C0085574,C538103,,MONDO:0001332,palindromic rheumatism,(Palindromic rheumatism) or (intermittent joint effusion) | Palindromic rheumatism | Intermittent joint effusion | Intermittent hydrarthrosis | Hench - Rosenberg syndrome | (Palindromic rheumatism) or (intermittent joint effusion) (disorder) | Palindromic rheumatism | Hench-Rosenberg syndrome | Palindromic rheumatism (disorder)
+BMGC_DS02768,BMG_DS003589,,Iron-Refractory Iron Deficiency Anemia,,,,,DOID:11252,microcytic anemia,C0085576,C562385,206200,MONDO:0008788,IRIDA syndrome,
+BMGC_DS02769,BMG_DS003590,300980002,Normocytic anemia,,,,,DOID:720,normocytic anemia,C0085577,,MTHU039167,MONDO:0004139,normocytic anemia,Normocytic anaemia | Normocytic anemia | Normocytic anemia (disorder)
+BMGC_DS02770,BMG_DS003591,,Thalassemia Minor,beta-Thalassemia,,,,,,C0085578,D017086,,,,
+BMGC_DS02771,BMG_DS003592,,Essential Hypertension,Essential Hypertension,,,,DOID:10825,essential hypertension,C0085580,D000075222,,MONDO:0001134,essential hypertension,
+BMGC_DS02772,BMG_DS003594,,Retrobulbar Neuritis,Optic Neuritis,,,,,,C0085582,D009902,,MONDO:0024335,retrobulbar neuritis,
+BMGC_DS02773,BMG_DS003595,43105007,Choreoathetosis,,,,,,,C0085583,,MTHU001903,,,Choreoathetosis | Choreoathetosis (disorder)
+BMGC_DS02774,BMG_DS003596,,Encephalopathies,Brain Diseases,,,,DOID:936,brain disease,C0085584,D001927,,,,
+BMGC_DS02775,BMG_DS003598,,Liver Failure,Liver Failure,,,,,,C0085605,D017093,MTHU072923,MONDO:0100192,liver failure,
+BMGC_DS02776,BMG_DS003599,44103008,Ventricular arrhythmia,,,,,,,C0085612,,MTHU006286,,,Ventricular arrhythmia | Ventricular arrhythmia (disorder)
+BMGC_DS02777,BMG_DS003600,270492004;195041009;14256006,First degree atrioventricular block,,,,,,,C0085614,,,MONDO:0000466,first-degree atrioventricular block,"First degree atrioventricular block | First degree heart block | Incomplete atrioventricular block, first degree | First degree atrioventricular block (disorder) | (Prolonged P-R interval) or (first degree AV block) | Prolonged P-R interval | Prolonged PR interval | First degree atrioventricular block | (Prolonged P-R interval) or (first degree AV block) (disorder) | First degree atrioventricular block | First degree atrioventricular block (disorder)"
+BMGC_DS02778,BMG_DS003601,195064006;195055001;155358002;59118001,Right bundle branch block,,,,,,,C0085615,,MTHU036516,,,Right bundle branch block | Right bundle branch block (disorder) | Right bundle branch block | Right bundle branch block (disorder) | Right fascicular block | RBBB - Right bundle branch block
+BMGC_DS02779,BMG_DS003602,267697002;155034007;86022000,Monoplegia,Hemiplegia,,,,,,C0085622,D006429,,,,Monoplegia | Diplegia | Paralytic syndromes NOS | (Paralytic syndromes NOS) or (diplegia) or (monoplegia) | (Paralytic syndromes NOS) or (diplegia) or (monoplegia) (disorder) | (Paralytic syndromes NOS) or (diplegia) or (monoplegia) | Paralytic syndromes NOS | Diplegia | Monoplegia | (Paralytic syndromes NOS) or (diplegia) or (monoplegia) (disorder) | Monoplegia | Monoplegia (disorder)
+BMGC_DS02780,BMG_DS003604,,,,,,,,,C0085637,,,MONDO:0000483,oculogyric crisis,
+BMGC_DS02781,BMG_DS003605,,Livedo Reticularis,Livedo Reticularis,,,,,,C0085642,D054068,,MONDO:0044037,livedo reticularis,
+BMGC_DS02782,BMG_DS003606,,Purpura Fulminans,Purpura Fulminans,,,,DOID:0060538,purpura fulminans,C0085650,D055665,,MONDO:0000809,purpura fulminans,
+BMGC_DS02783,BMG_DS003607,,Pyoderma Gangrenosum,Pyoderma Gangrenosum,,,,DOID:8553,pyoderma gangrenosum,C0085652,D017511,,MONDO:0018824,pyoderma gangrenosum,
+BMGC_DS02784,BMG_DS003608,,,,,,,,,C0085653,,,MONDO:0022096,pyogenic granuloma,
+BMGC_DS02785,BMG_DS003609,31384009;156457001,Polymyositis,Polymyositis,4A41.1Z,"Polymyositis, unspecified",M33.2,DOID:0080745,polymyositis,C0085655,D017285,MTHU037341,MONDO:0019127,polymyositis,Polymyositis | Neuromyositis | PM - Polymyositis | Polymyositis (disorder) | Polymyositis | Polymyositis (disorder)
+BMGC_DS02786,BMG_DS003610,156348006;267846008;81418003,Nummular eczema,,,,,,,C0085656,,,,,(Contact dermatitis NOS) or (discoid eczema) or (nummular eczema) | Contact dermatitis NOS | Nummular eczema | Discoid eczema | (Contact dermatitis NOS) or (discoid eczema) or (nummular eczema) (disorder) | Nummular eczema | Contact dermatitis NOS | Discoid eczema | (Contact dermatitis NOS) or (discoid eczema) or (nummular eczema) | (Contact dermatitis NOS) or (discoid eczema) or (nummular eczema) (disorder) | Nummular eczema | Nummular dermatitis | Nummular eczematous dermatitis | Nummular eczema (disorder) | Discoid eczema
+BMGC_DS02787,BMG_DS003619,,,,,,,DOID:12603,acute leukemia,C0085669,,,MONDO:0010643,acute leukemia,
+BMGC_DS02788,BMG_DS003620,,Alcoholic Neuropathy,Alcoholic Neuropathy,,,,DOID:14183,alcoholic neuropathy,C0085677,D020269,,MONDO:0006645,alcoholic polyneuropathy,
+BMGC_DS02789,BMG_DS003621,74450001,Hyperchloremia,,5C7Y,"Other specified disorders of fluid, electrolyte or acidbase balance",E87.8,,,C0085679,,MTHU069313,,,Hyperchloremia | Hyperchloraemia | Hyperchloremia (disorder)
+BMGC_DS02790,BMG_DS003622,10399008,Hypochloremia (disorder),,,,,,,C0085680,,,,,Hypochloremia | Hypochloraemia | Hypochloremia (disorder)
+BMGC_DS02791,BMG_DS003623,20165001,Hyperphosphatemia (disorder),,,,,DOID:0050459,hyperphosphatemia,C0085681,,,MONDO:0000328,hyperphosphatemia,Hyperphosphatemia | Hyperphosphataemia | Hyperphosphatemia (disorder)
+BMGC_DS02792,BMG_DS003624,4996001,Hypophosphatemia,Hypophosphatemia,,,,DOID:0050336,hypophosphatemia,C0085682,D017674,,MONDO:0000313,hypophosphatemia,Hypophosphatemia | Hypophosphataemia | Hypophosphatemia (disorder)
+BMGC_DS02793,BMG_DS003625,414521009;397514009,Internal hordeolum,,,,,DOID:9908,internal hordeolum,C0085690,,,MONDO:0004917,internal hordeolum,Internal hordeolum (disorder) | Internal hordeolum | Hordeolum internum | Infected chalazion | Infected cyst of meibomian gland | Infected meibomian cyst | Infection of meibomian gland | Meibomian adenitis | Internal hordeolum (disorder) | Internal hordeolum | Chalazion
+BMGC_DS02794,BMG_DS003629,8493009,Chronic gastritis,,,,,,,C0085695,,MTHU001681,MONDO:0005001,chronic gastritis,Chronic gastritis | Chronic gastritis (disorder) | CG - Chronic gastritis
+BMGC_DS02795,BMG_DS003631,123293005;155861006;63302006;266619007,Chronic pyelonephritis,,,,,DOID:1076,chronic pyelonephritis,C0085697,,MTHU036826,MONDO:0001110,chronic pyelonephritis,Chronic pyelonephritis | Chronic pyelonephritis (disorder) | (Chronic pyelonephritis) or (chronic pyonephrosis) | Chronic pyelonephritis | Chronic pyonephrosis | Pyonephrosis - chronic | (Chronic pyelonephritis) or (chronic pyonephrosis) (disorder) | Chronic pyelonephritis | Chronic pyelonephritis (disorder) | CPN - Chronic pyelonephritis | Chronic pyelonephritis | Chronic pyonephrosis | Pyonephrosis - chronic | (Chronic pyelonephritis) or (chronic pyonephrosis) | (Chronic pyelonephritis) or (chronic pyonephrosis) (disorder)
+BMGC_DS02796,BMG_DS003633,63198006,Chondromalacia,Cartilage Diseases,FB82.0Z,"Chondromalacia, unspecified",M94.2,DOID:2557,chondromalacia,C0085700,D002357,MTHU059240,MONDO:0005569;MONDO:0002342,obsolete cartilage disease | chondromalacia,Chondromalacia | Chondromalacia (disorder)
+BMGC_DS02797,BMG_DS003635,,Mendelson Syndrome,"Pneumonia, Aspiration",,,,,,C0085740,D011015,,,,
+BMGC_DS02798,BMG_DS003637,,,,,,,DOID:5998,microglandular adenosis,C0085750,,,MONDO:0003725,breast adenosis,
+BMGC_DS02799,BMG_DS003638,,,,,,,DOID:1574,alcohol use disorder,C0085762,,,MONDO:0002046,alcohol abuse,
+BMGC_DS02800,BMG_DS003640,155624004;196123009;233721005;266410004;45157009;129459004,Hamman-Rich syndrome,,,,J84.114,DOID:2797,idiopathic interstitial pneumonia,C0085786,,,,,Idiopath. fibrosing alveolitis (& Hamman-Rich syndrome) | Idiopath. fibrosing alveolitis | Alveolitis-idiopath. fibrosing | Fibrosing alveolitis-idiopath. | Hamman-Rich syndrome | Idiopathic fibrosing alveolitis | Idiopath. fibrosing alveolitis (& Hamman-Rich syndrome) (disorder) | Cryptogenic fibrosing alveolitis | Hamman-Rich syndrome | Idiopathic fibrosing alveolitis | Hamman - Rich syndrome | Fibrosing alveolitis: [idiopathic] or [cryptogenic]) or (Hamman - Rich syndrome) | Fibrosing alveolitis: [idiopathic] or [cryptogenic]) or (Hamman - Rich syndrome) (disorder) | Usual interstitial pneumonitis | Hamman-Rich syndrome | Usual interstitial pneumonitis (disorder) | Idiopath. fibrosing alveolitis (& Hamman-Rich syndrome) | Idiopath. fibrosing alveolitis | Hamman-Rich syndrome | Fibrosing alveolitis-idiopath. | Alveolitis-idiopath. fibrosing | Idiopathic fibrosing alveolitis | Idiopath. fibrosing alveolitis (& Hamman-Rich syndrome) (disorder) | Idiopathic fibrosing alveolitis | Idiopathic interstitial pneumonia | Idiopathic fibrosing alveolitis (disorder) | Hamman-Rich syndrome | Hamman-Rich disease | Acute interstitial pneumonia | Acute interstitial pneumonia (disorder)
+BMGC_DS02801,BMG_DS003642,,Anguilluliasis,Strongyloidiasis,,,,,,C0085810,D013322,,,,
+BMGC_DS02802,BMG_DS003643,,Antibiotic-Associated Colitis,"Enterocolitis, Pseudomembranous",,,,DOID:0060185,Clostridium difficile colitis,C0085819,D004761,,,,
+BMGC_DS02803,BMG_DS003644,,Polyglandular Type I Autoimmune Syndrome,"Polyendocrinopathies, Autoimmune",,,,,,C0085859,D016884,240300,MONDO:0009411,autoimmune polyendocrine syndrome type 1,
+BMGC_DS02804,BMG_DS003645,,"Autoimmune Syndrome Type II, Polyglandular","Polyendocrinopathies, Autoimmune",,,,,,C0085860,D016884,269200,MONDO:0010012,autoimmune polyendocrinopathy type 2,
+BMGC_DS02805,BMG_DS003647,,Bouillaud Disease,Rheumatic Heart Disease,,,,DOID:0050827,rheumatic heart disease,C0085916,D012214,,,,
+BMGC_DS02806,BMG_DS003648,,Brachial Neuralgia,Brachial Plexus Neuritis,,,,,,C0085920,D020968,,,,
+BMGC_DS02807,BMG_DS003652,,"Eczema, Infantile","Dermatitis, Atopic",,,,,,C0086196,D003876,,,,
+BMGC_DS02808,BMG_DS003653,266221005;154412007;266162007;19722001,Enterobiasis,Enterobiasis,,,B80,,,C0086227,D017229,,MONDO:0005746,enterobiasis,(Threadworms &/or enterobiasis) or (pinworm) | Threadworms | Threadworms - enterobiasis | Enterobiasis | Enterobiasis - threadworm | Pinworm | (Threadworms &/or enterobiasis) or (pinworm) (disorder) | (Threadworms &/or enterobiasis) or (pinworm) | Pinworm | Threadworms - enterobiasis | Threadworms | Enterobiasis - threadworm | Enterobiasis | (Threadworms &/or enterobiasis) or (pinworm) (disorder) | Enterobiasis | Oxyuriasis | Pinworm disease | Enterobiasis - threadworm | Pinworm infection | Threadworm infection | Enterobiosis | Enterobiasis (disorder) | Infection by Enterobius vermicularis | Infection by Enterobius vermicularis (disorder)
+BMGC_DS02809,BMG_DS003654,,"Epilepsy, Atonic","Epilepsy, Generalized",,,,,,C0086236,D004829,,,,
+BMGC_DS02810,BMG_DS003655,,"Epilepsy, Cryptogenic",Epilepsy,,,,,,C0086237,D004827,,,,
+BMGC_DS02811,BMG_DS003657,,"Epilepsy, Simple Partial","Epilepsies, Partial",,,,,,C0086240,D004828,,,,
+BMGC_DS02812,BMG_DS003658,,"Epilepsy, Tonic","Epilepsy, Generalized",,,,,,C0086241,D004829,,,,
+BMGC_DS02813,BMG_DS003659,,Essential Polyarteritis,Polyarteritis Nodosa,,,,,,C0086254,D010488,,,,
+BMGC_DS02814,BMG_DS003660,,Gonadotropin-Resistant Ovary Syndrome,Primary Ovarian Insufficiency,,,,,,C0086367,D016649,,,,
+BMGC_DS02815,BMG_DS003661,,Granuloma Gangraenescens,"Granuloma, Lethal Midline",,,,,,C0086370,D006103,,,,
+BMGC_DS02816,BMG_DS003662,,Hereditary Sensory Radicular Neuropathy,Hereditary Sensory and Autonomic Neuropathies,,,,DOID:0050548,hereditary sensory neuropathy,C0086405,D009477,,,,
+BMGC_DS02817,BMG_DS003663,,Hurler-Scheie Syndrome,Mucopolysaccharidosis I,,,,DOID:0111389,mucopolysaccharidosis Ih/s,C0086431,D008059,607015,MONDO:0011759,Hurler-Scheie syndrome,
+BMGC_DS02818,BMG_DS003664,,"Hyalinosis, Segmental Glomerular","Glomerulosclerosis, Focal Segmental",,,,,,C0086432,D005923,,,,
+BMGC_DS02819,BMG_DS003665,119250001,Hypogammaglobulinemia,Agammaglobulinemia,,,,DOID:2583,agammaglobulinemia,C0086438,D000361,MTHU001684,,,Hypogammaglobulinemia | Hypogammaglobulinaemia | Hypogammaglobulinemia (finding)
+BMGC_DS02820,BMG_DS003666,,Idiopathic Membranous Glomerulonephritis,"Glomerulonephritis, Membranous",,,,,,C0086445,D015433,614692,MONDO:0013860,idiopathic membranous glomerulonephritis,
+BMGC_DS02821,BMG_DS003667,,Industrial Dermatosis,"Dermatitis, Occupational",,,,,,C0086457,D009783,,,,
+BMGC_DS02822,BMG_DS003669,,"Leishmaniasis, New World","Leishmaniasis, Cutaneous",,,,,,C0086540,D016773,,,,
+BMGC_DS02823,BMG_DS003671,155126003;62795009;193570009;128306009,Cataract,Cataract,,,,,,C0086543,D002386,MTHU004637,MONDO:0005129,cataract,Cataract | Cataract (disorder) | Cataract | Lenticular opacity | Cataract (disorder) | Lens opacity | Cataract | Cataract (morphologic abnormality)
+BMGC_DS02824,BMG_DS003674,267495004;154730001,Marasmus,Protein-Energy Malnutrition,,,,DOID:12328,marasmus,C0086588,D011502,,MONDO:0006848,marasmus,Nutritional deficiencies: (& [dietary] or [kwashiokor] or [marasmus]) | Dietary deficiency | Marasmus | Insufficiency - dietary | Nutritional deficiencies | Deficiency -nutritional | Kwashiorkor | Kwashiokor | Nutritional deficiencies: (& [dietary] or [kwashiokor] or [marasmus]) (disorder) | Kwashiokor | Deficiency -nutritional | Marasmus | Kwashiorkor | Nutritional deficiencies | Insufficiency - dietary | Dietary deficiency | Nutritional deficiencies: (& [dietary] or [kwashiokor] or [marasmus]) | Nutritional deficiencies: (& [dietary] or [kwashiokor] or [marasmus]) (disorder)
+BMGC_DS02825,BMG_DS003675,,Minamata Disease,"Mercury Poisoning, Nervous System",,,,,,C0086626,D020262,,MONDO:0024251,Minamata disease,
+BMGC_DS02826,BMG_DS003676,,Mucopolysaccharidosis Type IIIA,Mucopolysaccharidosis III,,,,DOID:0111395,mucopolysaccharidosis type IIIA,C0086647,D009084,252900,MONDO:0009655,mucopolysaccharidosis type 3A,
+BMGC_DS02827,BMG_DS003677,,Mucopolysaccharidosis Type IIIB,Mucopolysaccharidosis III,,,,DOID:0111394,mucopolysaccharidosis type IIIB,C0086648,D009084,252920,MONDO:0009656,mucopolysaccharidosis type 3B,
+BMGC_DS02828,BMG_DS003678,,MPS III C,Mucopolysaccharidosis III,,,,DOID:0111393,mucopolysaccharidosis type IIIC,C0086649,D009084,252930,MONDO:0009657,mucopolysaccharidosis type 3C,
+BMGC_DS02829,BMG_DS003679,,MPS III D,Mucopolysaccharidosis III,,,,DOID:0111402,mucopolysaccharidosis type IIID,C0086650,D009084,252940,MONDO:0009658,mucopolysaccharidosis type 3D,
+BMGC_DS02830,BMG_DS003680,7259005,"Mucopolysaccharidosis, MPS-IV-A",,,,,DOID:0111391,mucopolysaccharidosis IVA,C0086651,,253000,MONDO:0009659,mucopolysaccharidosis type 4A,"Mucopolysaccharidosis, MPS-IV-A | Morquio's syndrome, classic form | N-acetylgalactosamine-6-sulfatase deficiency | Morquio A syndrome | N-acetylgalactosamine-6-sulphatase deficiency | Galactose-6-sulphatase deficiency | Galactosamine-6-sulphatase deficiency | Galactose-6-sulfatase deficiency | Galactosamine-6-sulfatase deficiency | MPS IV-A-Mucopolysaccharidosis IV-A | Mucopolysaccharidosis IV-A | Morquio syndrome A | Mucopolysaccharidosis IV-A (disorder)"
+BMGC_DS02831,BMG_DS003681,238044004;254075008,Mucopolysaccharidosis type IVB,,,,,DOID:0111392,mucopolysaccharidosis type IVB,C0086652,,253010,MONDO:0009660,mucopolysaccharidosis type 4B,"Mucopolysaccharidosis, MPS-IV-B | MPS IV-B - Mucopolysaccharidosis IV-B | Morquio B syndrome | Morquio syndrome B | Mucopolysaccharidosis IV-B | Mucopolysaccharidosis type IVB | Morquio-like syndrome | Mucopolysaccharidosis type IVB (disorder) | Mucopolysaccharidosis type IVB | Mucopolysaccharidosis type IVB (disorder)"
+BMGC_DS02832,BMG_DS003682,,,,,,,DOID:0060326,myelomeningocele,C0086664,,,,,
+BMGC_DS02833,BMG_DS003683,,Myocardial Preinfarction Syndrome,"Angina, Unstable",,,,,,C0086666,D000789,,,,
+BMGC_DS02834,BMG_DS003684,,,,,,,,,C0086692,,,MONDO:0005165,benign neoplasm,
+BMGC_DS02835,BMG_DS003685,,Osteoarthrosis Deformans,Osteoarthritis,,,,,,C0086743,D010003,,,,
+BMGC_DS02836,BMG_DS003686,,,,,,,DOID:6977,pancreatic cholera,C0086768,,,MONDO:0004058,pancreatic cholera,
+BMGC_DS02837,BMG_DS003687,,,,,,,DOID:0060284,paroxysmal nocturnal hemoglobinuria,C0086774,,,MONDO:0019533,paroxysmal cold hemoglobinuria,
+BMGC_DS02838,BMG_DS003689,,Pfaundler-Hurler Syndrome,Mucopolysaccharidosis I,,,,DOID:0111390,mucopolysaccharidosis Ih,C0086795,D008059,607014,MONDO:0011758,Hurler syndrome,
+BMGC_DS02839,BMG_DS003690,,Plantar Ulcer,Foot Ulcer,,,,,,C0086815,D016523,,,,
+BMGC_DS02840,BMG_DS003691,201151002;31471004;238731001,Pseudopelade,Alopecia,ED70.5Y,Scarring alopecia due to other specified cause,L66.0,,,C0086873,D000505,,MONDO:0015261,pseudopelade of Brocq,Pseudopelade | Pseudopelade (disorder) | Alopecia cicatrisata | Pseudopelade | Pseudopelade of Brocq | Cicatricial alopecia | Scarring alopecia | Alopecia cicatrisata (disorder) | Pseudopelade | Pseudopelade (disorder) | Pseudopelade of Brocq
+BMGC_DS02841,BMG_DS003692,,Rheumatoid Purpura,IgA Vasculitis,,,,,,C0086922,D011695,,,,
+BMGC_DS02842,BMG_DS003696,,Sicca Syndrome,Sjogren's Syndrome,,,,DOID:12894,Sjogren's syndrome,C0086981,D012859,,,,
+BMGC_DS02843,BMG_DS003697,,"Ataxia, Spinocerebellar",Spinocerebellar Ataxias,,,,DOID:1441,autosomal dominant cerebellar ataxia,C0087012,D020754,,,,
+BMGC_DS02844,BMG_DS003698,,Juvenile-Onset Still Disease,"Arthritis, Juvenile",,,,,,C0087031,D001171,,,,
+BMGC_DS02845,BMG_DS003701,2589008,Acute dacryoadenitis,,,,H04.01,DOID:952,acute dacryoadenitis,C0149505,,,MONDO:0004812,acute dacryoadenitis,Acute dacryoadenitis | Acute dacryoadenitis (disorder)
+BMGC_DS02846,BMG_DS003702,193990009;84627005,Chronic dacryocystitis,,,,H04.41,DOID:9937,chronic dacryocystitis,C0149506,,,MONDO:0004925,chronic dacryocystitis,Chronic inflammation of lacrimal passage (& [dacryocystitis]) | Dacryocystitis - chronic | Chronic inflammation of lacrimal passage | Chronic dacryocystitis | Chronic inflammation of lacrimal passage (& [dacryocystitis]) (disorder) | Chronic dacryocystitis | Chronic dacryocystitis (disorder)
+BMGC_DS02847,BMG_DS003703,,Orbital Cellulitis,Orbital Cellulitis,,,,DOID:11234,orbital cellulitis,C0149507,D054517,,MONDO:0006881,orbital cellulitis,
+BMGC_DS02848,BMG_DS003705,15805002;155498004;195649005,Acute sinusitis,,,,J01,DOID:0050127,sinusitis,C0149512,,,,,Acute sinusitis | Acute inflammation of nasal sinus | Acute sinusitis (disorder) | Acute inflammation of sinus | Acute infection of sinus | Acute sinusitis | Acute sinusitis (disorder) | Sinusitis (& acute) | Acute sinusitis | Sinusitis | Sinusitis (& acute) (disorder)
+BMGC_DS02849,BMG_DS003706,26650005;155507000,Acute tracheitis,,CA05.1,Acute tracheitis,J04.1,DOID:9392,tracheitis,C0149513,,,,,Acute tracheitis | Acute tracheitis (disorder)
+BMGC_DS02850,BMG_DS003707,155512004;10509002;266380005;195713004,Acute bronchitis,,,,J20,DOID:6132,bronchitis,C0149514,,,,,Acute: [bronchitis] or [chest infections] or [tracheobronchitis] | Acute chest infections | Bronchitis - acute | Acute tracheobronchitis | Acute bronchitis | Tracheobronchitis - acute | Acute: [bronchitis] or [chest infections] or [tracheobronchitis] (disorder) | Acute bronchitis | Acute bronchitis (disorder) | Acute: [bronchitis] or [chest infections] or [tracheobronchitis] | Acute chest infections | Acute tracheobronchitis | Bronchitis - acute | Acute bronchitis | Tracheobronchitis - acute | Acute: [bronchitis] or [chest infections] or [tracheobronchitis] (disorder) | Acute bronchitis (& wheezy) | Subacute bronchitis | Acute wheezy bronchitis | Acute bronchitis | Acute bronchitis (& wheezy) (disorder)
+BMGC_DS02851,BMG_DS003708,155525007;40055000,Chronic sinusitis,,,,J32,,,C0149516,,MTHU037623,MONDO:0006031,chronic rhinosinusitis,Chronic sinusitis | Chronic sinusitis (disorder) | Chronic sinusitis | Chronic sinusitis (disorder) | Chronic infection of sinus
+BMGC_DS02852,BMG_DS003709,155530006;90979004;195794009,Chronic tonsillitis,,,,J35.01,DOID:10456,tonsillitis,C0149517,,,,,Chronic tonsillitis | Chronic tonsillitis (disorder) | Chronic adenoiditis | Chronic tonsillitis | (Chronic tonsillitis) or (chronic adenoiditis) | (Chronic tonsillitis) or (chronic adenoiditis) (disorder)
+BMGC_DS02853,BMG_DS003711,,Chronic Persistent Hepatitis,"Hepatitis, Chronic",,,,DOID:2237,hepatitis,C0149519,D006521,,,,
+BMGC_DS02854,BMG_DS003713,,"Pancreatitis, Chronic","Pancreatitis, Chronic",,,,,,C0149521,D050500,,MONDO:0005003,chronic pancreatitis,
+BMGC_DS02855,BMG_DS003715,68226007;266628008;197833009;155883005,Acute cystitis,,XT5R;GC00.1,Acute | Infectious cystitis,N30.0,DOID:13148,acute cystitis,C0149523,,,MONDO:0001650,acute cystitis,Acute cystitis | Acute cystitis (disorder) | Acute recurrent cystitis | Recurrent acute cystitis | Acute cystitis | Acute cystitis (& [recurrent]) | Acute cystitis (& [recurrent]) (disorder) | Acute cystitis (& [recurrent]) | Acute cystitis | Acute recurrent cystitis | Recurrent acute cystitis | Acute cystitis (& [recurrent]) (disorder)
+BMGC_DS02856,BMG_DS003717,155934005;85324003,Calculus of prostate,,GA91.3,Calculus of prostate,N42.0,DOID:13689,prostate calculus,C0149525,,,MONDO:0001776,prostate calculus,Calculus of prostate | Calculus of prostate (disorder) | Calculus of prostate | Prostatic stone | Prostatic lithiasis | Stone of prostate | Calculus of prostate (disorder)
+BMGC_DS02857,BMG_DS003718,40178009;156428000;201260002,Allergic urticaria,,EM0Z,Skin disease of unspecified nature,L50.0,DOID:10612,allergic urticaria,C0149526,,,MONDO:0006526,allergic urticaria,Allergic urticaria | Allergic urticaria (disorder) | Urticaria: [allergic] or [drug induced] | Drug induced urticaria | Allergic urticaria | Urticaria: [allergic] or [drug induced] (disorder)
+BMGC_DS02858,BMG_DS003719,204381004;46619002;156924006,Congenital heart block,,LA8Y,Other specified structural developmental anomaly of heart or great vessels,Q24.6,DOID:990,congenital heart block,C0149530,C535758,234700,MONDO:0009326,congenital heart block,Congenital heart block | Congenital heart block (disorder)
+BMGC_DS02859,BMG_DS003721,,"Neurogenic Urinary Bladder, Atonic","Urinary Bladder, Neurogenic",,,,,,C0149622,D001750,,MONDO:0001445,obsolete neurogenic bladder,
+BMGC_DS02860,BMG_DS003725,,,,,,,DOID:1519,cecum carcinoma,C0149640,,,MONDO:0006029,cecum carcinoma,
+BMGC_DS02861,BMG_DS003726,3502005,Cervical lymphadenitis,,,,,DOID:4637,cervical adenitis,C0149642,,,MONDO:0003067,cervical lymphadenitis,Cervical lymphadenitis | Cervical adenitis | Cervical lymphadenitis (disorder)
+BMGC_DS02862,BMG_DS003728,,Cholesterol Embolism,"Embolism, Cholesterol",,,,DOID:1461,cholesterol embolism,C0149649,D017700,,MONDO:0005568,cholesterol embolism,
+BMGC_DS02863,BMG_DS003731,,,,,,,DOID:12995,conduct disorder,C0149654,,,MONDO:0005352,conduct disorder,
+BMGC_DS02864,BMG_DS003732,20957000,Disorder of carbohydrate metabolism,,,,,DOID:2978,carbohydrate metabolic disorder,C0149670,,,MONDO:0037792,carbohydrate metabolism disease,Disorder of carbohydrate metabolism | Disorder of carbohydrate metabolism (disorder)
+BMGC_DS02865,BMG_DS003733,,Epstein-Barr Virus Infections,Epstein-Barr Virus Infections,,,,DOID:2938,Epstein-Barr virus infectious disease,C0149678,D020031,,MONDO:0005111,Epstein-Barr virus infection,
+BMGC_DS02866,BMG_DS003735,155644005;266490003;20607006,Gingivostomatitis,,,,,,,C0149704,,MTHU070633,,,(Chronic gingivitis) or (gingivostomatitis) | Gingivostomatitis | Chronic gingivitis | (Chronic gingivitis) or (gingivostomatitis) (disorder) | Gingivostomatitis | Gingivostomatitis (disorder)
+BMGC_DS02867,BMG_DS003736,,Left Ventricular Hypertrophy,"Hypertrophy, Left Ventricular",,,,,,C0149721,D017379,,,,
+BMGC_DS02868,BMG_DS003737,50417007;195745009,Lower respiratory tract infection,,,,,,,C0149725,,,,,Lower respiratory tract infection | Lower respiratory infection | Chest cold | Lower respiratory tract infection (disorder) | LRTI - Lower respiratory tract infection | Respiratory tract infection (& [acute lower] or [lower]) | Lower respiratory tract infection | RTI - Respiratory tract infection | Acute lower respiratory tract infection | Respiratory tract infection | Lower resp tract infection | Respiratory tract infection (& [acute lower] or [lower]) (disorder)
+BMGC_DS02869,BMG_DS003738,,Oral Ulcer,Oral Ulcer,,,,,,C0149745,D019226,,,,
+BMGC_DS02870,BMG_DS003740,,"Fasciitis, Plantar","Fasciitis, Plantar",,,,DOID:9600,plantar fasciitis,C0149756,D036981,,MONDO:0004833,plantar fasciitis,
+BMGC_DS02871,BMG_DS003746,155610003;80423007,Spontaneous pneumothorax,,,,,,,C0149781,,MTHU018164,,,Spontaneous pneumothorax | Spontaneous pneumothorax (disorder)
+BMGC_DS02872,BMG_DS003747,,,,,,,DOID:3907,lung squamous cell carcinoma,C0149782,,,MONDO:0005097,squamous cell lung carcinoma,
+BMGC_DS02873,BMG_DS003754,111591002,Hypertrophy of adenoids,,CA0F.1,Hypertrophy of adenoids,J35.2,DOID:0060311,adenoid hypertrophy,C0149825,,,,,Hypertrophy of adenoids | Enlargement of adenoids | Adenoidal hypertrophy | Adenoidal enlargement | Hypertrophy of adenoids (disorder)
+BMGC_DS02874,BMG_DS003760,,,,,,,DOID:5391,bronchus adenoma,C0149845,,,MONDO:0003427,bronchus adenoma,
+BMGC_DS02875,BMG_DS003761,221695002;87494005;202879008,Achilles bursitis,,FB40.Y,Other specified tenosynovitis,M76.6,DOID:12857,Achilles bursitis,C0149846,,,MONDO:0001594,Achilles bursitis,Achilles bursitis | Achillobursitis | Albert's syndrome | Swediaur's disease | Capped hock | Bursitis of calcaneal tendon bursa (disorder) | Bursitis of calcaneal tendon bursa | Achilles bursitis | Calcaneal osteochondritis | Achilles bursitis (disorder) | Achilles bursitis | Haglund's deformity | Achilles bursitis (disorder)
+BMGC_DS02876,BMG_DS003766,,Spasmodic Croup,Croup,,,,,,C0149869,D003440,,,,
+BMGC_DS02877,BMG_DS003767,,De Quervain Disease,De Quervain Disease,,,,DOID:14107,De Quervain disease,C0149870,D053684,,MONDO:0006721,de Quervain disease,
+BMGC_DS02878,BMG_DS003768,,Deep Vein Thrombosis,Venous Thrombosis,,,,,,C0149871,D020246,,,,
+BMGC_DS02879,BMG_DS003770,,hypoglycemic encephalopathy,,,,,,,C0149877,C000721848,,,,
+BMGC_DS02880,BMG_DS003773,24084007;197983000;155915005,Epididymo-orchitis,,,,N45.3,DOID:9401,epididymo-orchitis,C0149881,,,MONDO:0004778,epididymo-orchitis,Epididymo-orchitis | Epididymo-orchitis (disorder) | Orchitis and epididymitis | Orchitis and epididymitis (disorder) | Epididymo-orchitis | Inflammation of testis and epididymis
+BMGC_DS02881,BMG_DS003775,,"Seizure, Febrile, Simple","Seizures, Febrile",,,,,,C0149886,D003294,,,,
+BMGC_DS02882,BMG_DS003776,,Slipped Capital Femoral Epiphyses,Slipped Capital Femoral Epiphyses,,,,,,C0149887,D060048,182260,MONDO:0018382,epiphysiolysis of the hip,
+BMGC_DS02883,BMG_DS003778,95717004,Secondary glaucoma,,,,,,,C0149893,,MTHU048421,,,Secondary glaucoma | Secondary glaucoma (disorder) | Glaucoma due to ocular disease
+BMGC_DS02884,BMG_DS003780,95556007,Cholestatic hepatitis,,,,,,,C0149904,,MTHU070763,,,Cholestatic hepatitis | Cholestatic hepatitis (disorder)
+BMGC_DS02885,BMG_DS003783,47709007,Humoral hypercalcemia of malignancy (disorder),,,,,,,C0149911,,,MONDO:0043455,humoral hypercalcemia of malignancy,Humoral hypercalcemia of malignancy | Malignancy associated hypercalcemia | Malignancy associated hypercalcaemia | Humoural hypercalcaemia of malignancy | Humoral hypercalcemia of malignancy (disorder) | Hypercalcaemia of malignancy | Malignant hypercalcaemia | Hypercalcemia of malignancy | Malignant hypercalcemia | HHM - humoral hypercalcemia of malignancy | MAHC - malignancy associated hypercalcaemia | MAHC - malignancy associated hypercalcemia | HHM - humoral hypercalcaemia of malignancy
+BMGC_DS02886,BMG_DS003784,,Lichen Simplex Chronicus,Neurodermatitis,,,,,,C0149922,D009450,,,,
+BMGC_DS02887,BMG_DS003785,,,,,,,DOID:5409,lung small cell carcinoma,C0149925,,182280,MONDO:0008433,small cell lung carcinoma,
+BMGC_DS02888,BMG_DS003787,,Migraine Disorders,Migraine Disorders,,,,DOID:6364,migraine,C0149931,D008881,,MONDO:0005277,migraine disorder,
+BMGC_DS02889,BMG_DS003788,86249007,Obstructive nephropathy,,,,,DOID:0070314,obstructive nephropathy,C0149939,,,MONDO:0056796,obstructive nephropathy,Obstructive nephropathy | Obstructive nephropathy (disorder)
+BMGC_DS02890,BMG_DS003789,,Sciatic Neuropathy,Sciatic Neuropathy,,,,DOID:11446,sciatic neuropathy,C0149940,D020426,,MONDO:0006960,sciatic neuropathy,
+BMGC_DS02891,BMG_DS003791,30250000,Acute otitis externa,,,,,,,C0149948,,,MONDO:0001051,acute otitis externa,Acute otitis externa | Acute otitis externa (disorder)
+BMGC_DS02892,BMG_DS003792,,,,,,,,,C0149951,,166970,MONDO:0008168,ovarian fibroma,
+BMGC_DS02893,BMG_DS003793,,,,,,,DOID:0060850,annular pancreas,C0149955,,167750,MONDO:0008183,annular pancreas,
+BMGC_DS02894,BMG_DS003799,74372003,Gonorrhea of pharynx,,,,,,,C0149966,,,,,Gonorrhea of pharynx | Gonorrhoea of pharynx | Gonorrhea of pharynx (disorder) | Gonococcal pharyngitis
+BMGC_DS02895,BMG_DS003803,,,,,,,DOID:1996,rectum adenocarcinoma,C0149978,,,MONDO:0002169,rectum adenocarcinoma,
+BMGC_DS02896,BMG_DS003806,,"Syphilis, secondary",,,,,DOID:4157,secondary syphilis,C0149985,C536773,,MONDO:0002897,secondary syphilis,
+BMGC_DS02897,BMG_DS003816,,Chronic Headache,Headache Disorders,,,,,,C0151293,D020773,,,,
+BMGC_DS02898,BMG_DS003817,,Mononeuritis Multiplex,Mononeuropathies,,,,DOID:1835,mononeuritis multiplex,C0151295,D020422,,MONDO:0002128,mononeuritis multiplex,
+BMGC_DS02899,BMG_DS003818,,Cranial nerve palsies,,,,,DOID:3817,cranial nerve palsy,C0151311,,MTHU005584,MONDO:0002782,cranial nerve palsy,
+BMGC_DS02900,BMG_DS003819,95662005,Sensory neuropathy,,,,,DOID:2491,sensory peripheral neuropathy,C0151313,,MTHU001836,MONDO:0002321,sensory peripheral neuropathy,Sensory neuropathy | Sensory neuropathy (disorder)
+BMGC_DS02901,BMG_DS003820,,Chronic Infection,Persistent Infection,,,,,,C0151317,D000088562,,,,
+BMGC_DS02902,BMG_DS003822,427099000,Active tuberculosis,,,,,,,C0151332,,,MONDO:0100481,active tuberculosis,Active tuberculosis (disorder) | Active tuberculosis
+BMGC_DS02903,BMG_DS003825,,"Vasculitis, Leukocytoclastic, Cutaneous","Vasculitis, Leukocytoclastic, Cutaneous",,,,DOID:9809,hypersensitivity vasculitis,C0151436,D018366,,MONDO:0001290,allergic cutaneous vasculitis,
+BMGC_DS02904,BMG_DS003832,237757001;190526004;267483004;154707007;190522002;766986002;24867002,Addisonian crisis,,5A74.1,Adrenal crisis,E27.2,,,C0151467,,MTHU058969,MONDO:0019801,acute adrenal insufficiency,Addisonian crisis | Addisonian crisis (disorder) | Corticoadrenal insufficiency | Addison's disease | Addisonian crisis | Corticoadrenal insufficiency (& Addison's [disease] or [crisis]) | Corticoadrenal insufficiency (& Addison's [disease] or [crisis]) (disorder) | Corticoadrenal insufficiency (& Addison's [disease] or [crisis]) | Addison's disease | Corticoadrenal insufficiency | Addisonian crisis | Corticoadrenal insufficiency (& Addison's [disease] or [crisis]) (disorder) | Acute adrenal insufficiency (& [Addisonian crisis] or [adrenal crisis]) | Addisonian crisis | Acute adrenal insufficiency | Adrenal crisis | Acute adrenal insufficiency (& [Addisonian crisis] or [adrenal crisis]) (disorder) | Acute adrenal failure | Acute adrenal insufficiency | Adrenocortical crisis | Adrenal crisis | Addisonian crisis | Acute adrenal insufficiency (disorder) | Acute adrenocortical insufficiency | Severe adrenal insufficiency | Severe adrenal insufficiency (disorder)
+BMGC_DS02905,BMG_DS003833,,,,,,,DOID:2891,thyroid adenoma,C0151468,,,,,
+BMGC_DS02906,BMG_DS003834,70134007,Hypochloremic alkalosis,,,,,,,C0151476,,,,,Hypochloremic alkalosis | Hypochloraemic alkalosis | Hypochloremic alkalosis (disorder)
+BMGC_DS02907,BMG_DS003835,85649008,Megaloblastic anemia due to folate deficiency,,,,,DOID:14026,folic acid deficiency anemia,C0151482,,,MONDO:0001860,folic acid deficiency anemia,Megaloblastic anemia due to folate deficiency | Folate deficiency anemia | Folic acid deficiency anemia | Megaloblastic anaemia due to folate deficiency | Folate deficiency anaemia | Folic acid deficiency anaemia | Megaloblastic anemia due to folate deficiency (disorder)
+BMGC_DS02908,BMG_DS003837,400190005;16343004,Atrophic condition of skin,,,,,DOID:2733,skin atrophy,C0151514,,,MONDO:0006610,skin atrophy,Atrophic condition of skin (disorder) | Atrophic condition of skin | Atrophy of skin | Skin atrophy | Atrophic skin | Atrophoderma | Atrophic condition of skin | Atrophy of skin | Atrophoderma | Skin atrophy | Atrophic skin | Atrophic condition of skin (disorder)
+BMGC_DS02909,BMG_DS003838,,Thyroid Hypoplasia,Thyroid Dysgenesis,,,,,,C0151516,D050033,,MONDO:0019861,thyroid hypoplasia,
+BMGC_DS02910,BMG_DS003839,27885002;195063000;155355004,Complete atrioventricular block,,,,,,,C0151517,,,MONDO:0000468,third-degree atrioventricular block,Complete atrioventricular block | Third degree atrioventricular block | Third degree heart block | Complete heart block | CHB - Complete heart block | Complete atrioventricular block (disorder) | High grade atrioventricular block | Complete atrioventricular block | Complete atrioventricular block (disorder)
+BMGC_DS02911,BMG_DS003841,,,,,,,,,C0151544,,,MONDO:0006181,digestive system carcinoma,
+BMGC_DS02912,BMG_DS003843,418072004,Central nervous system depression (disorder),,,,,,,C0151559,,,,,Central nervous system depression (disorder) | Central nervous system depression
+BMGC_DS02913,BMG_DS003848,95545007,Hemorrhagic diarrhea,,,,,,,C0151594,,,,,Hemorrhagic diarrhea | Bloody diarrhea | Bloody diarrhoea | Haemorrhagic diarrhoea | Hemorrhagic diarrhea (disorder)
+BMGC_DS02914,BMG_DS003849,,Hypertensive Encephalopathy,Hypertensive Encephalopathy,,,,DOID:9427,hypertensive encephalopathy,C0151620,D020343,,MONDO:0006796,hypertensive encephalopathy,
+BMGC_DS02915,BMG_DS003850,418632009,Endometrial disorder,,,,,DOID:1005,endometrial disease,C0151622,,,MONDO:0000931,endometrial disorder,Endometrial disorder (disorder) | Endometrial disorder
+BMGC_DS02916,BMG_DS003852,,Premature ventricular contractions,,,,,,,C0151636,,MTHU042669,,,
+BMGC_DS02917,BMG_DS003853,,Fanconi like syndrome,,,,,DOID:0090066,Fanconi-like syndrome,C0151638,C536855,227850,MONDO:0009217,Fanconi-like syndrome,
+BMGC_DS02918,BMG_DS003854,197660000,Renal fibrosis,,,,,,,C0151650,,MTHU073879,MONDO:0000494,renal fibrosis,Renal fibrosis | Renal fibrosis (disorder)
+BMGC_DS02919,BMG_DS003857,51875005,Gastrointestinal perforation,,,,,,,C0151664,,,,,Gastrointestinal perforation | Gastrointestinal perforation (disorder)
+BMGC_DS02920,BMG_DS003859,,,,,,,,,C0151691,,,MONDO:0017773,hypoalphalipoproteinemia,
+BMGC_DS02921,BMG_DS003860,66978005,Hypermagnesemia,,,,E83.41,,,C0151714,,,,,Hypermagnesemia | Hypermagnesaemia | Hypermagnesemia (disorder)
+BMGC_DS02922,BMG_DS003861,61336008,Hypocholesterolemia,,,,,,,C0151718,,MTHU009711,,,Hypocholesterolemia | Hypocholesteremia | Hypocholesterolaemia | Hypocholesteraemia | Hypocholesterolemia (disorder)
+BMGC_DS02923,BMG_DS003862,190557004;30187002;48723006,Testicular hypogonadism,,,,,,,C0151721,,241100,MONDO:0009421,"hypogonadism, male","(Hypogonadism: [eunuchoidism] or [testicular]) or (other testicular hypofunction) | Testicular hypogonadism | Other testicular hypofunction | Eunuchoidism, hypogonadism | Eunuchoidism hypogonadism | (Hypogonadism: [eunuchoidism] or [testicular]) or (other testicular hypofunction) (disorder) | Testicular hypogonadism | Testicular hypogonadism (disorder) | Male hypogonadism | Eunuchoidism hypogonadism | Primary gonadal failure | Testicular hypogonadism | Eunuchoidism | Testicular failure | Primary male hypogonadism | Male hypogonadism (disorder) | Eunuchoidism, hypogonadism"
+BMGC_DS02924,BMG_DS003863,82020005;190855004,Hypomagnesemia,,,,E83.42,,,C0151723,,MTHU036920,MONDO:0018100,familial primary hypomagnesemia,Hypomagnesemia | Hypomagnesaemia | Hypomagnesemia (disorder) | Hypomagnesaemia | Hypomagnesemia | Hypomagnesemia (disorder)
+BMGC_DS02925,BMG_DS003864,,Hepatic Infarction,Hepatic Infarction,,,,DOID:13738,hepatic infarction,C0151731,D000081011,,MONDO:0001787,hepatic infarction,
+BMGC_DS02926,BMG_DS003865,,,,,,,DOID:9428,intracranial hypertension,C0151740,,,MONDO:0006810,intracranial hypertension,
+BMGC_DS02927,BMG_DS003866,,Myocardial Ischemia,Myocardial Ischemia,,,,DOID:3393,coronary artery disease,C0151744,D017202,,MONDO:0024644,myocardial ischemia,
+BMGC_DS02928,BMG_DS003867,95568003,Renal tubular disorder,,,,,,,C0151747,,,MONDO:0021568,renal tubule disorder,Renal tubular disorder | Renal tubular disorder (disorder)
+BMGC_DS02929,BMG_DS003868,307762000;191398002;58642009,Bone marrow depression,,,,,,,C0151773,,,,,Bone marrow depression | Bone marrow depression (disorder) | Bone marrow failure | Bone marrow depression | Bone marrow depression (disorder) | Hypoplasia of bone marrow | Medullary hypoplasia | Bone marrow depression | Hypoplasia of bone marrow (disorder)
+BMGC_DS02930,BMG_DS003869,,,,,,,DOID:8923,skin melanoma,C0151779,,,MONDO:0005012,cutaneous melanoma,
+BMGC_DS02931,BMG_DS003870,95351003,Disease of mucous membrane,,,,,,,C0151785,,,,,Disease of mucosa | Mucous membrane disorder | Mucosal disease | Disorder of mucous membrane (disorder) | Disorder of mucous membrane
+BMGC_DS02932,BMG_DS003873,87248009,Hepatic necrosis,,,,,,,C0151798,,MTHU012736,,,Hepatic necrosis | Liver necrosis | Hepatic necrosis (disorder)
+BMGC_DS02933,BMG_DS003874,,Coronary Occlusion,Coronary Occlusion,,,,,,C0151814,D054059,,,,
+BMGC_DS02934,BMG_DS003875,46606001,Perforated corneal ulcer,,,,H16.07,DOID:10445,perforated corneal ulcer,C0151844,,,MONDO:0001038,perforated corneal ulcer,Perforated corneal ulcer | Perforated corneal ulcer (disorder)
+BMGC_DS02935,BMG_DS003877,91454002,Pleocytosis,Leukocytosis,,,,,,C0151857,D007964,,,,Pleocytosis | Pleocytosis of cerebrospinal fluid (finding) | Pleocytosis of cerebrospinal fluid
+BMGC_DS02936,BMG_DS003880,44574006,Porphyruria,,,,,,,C0151861,,,,,Porphyruria | Porphyrinuria | Hematoporphyrinuria | Pink tooth | Haematoporphyrinuria | Porphyruria (disorder)
+BMGC_DS02937,BMG_DS003881,172422001;23288008;173300003,Disorder of pregnancy,,,,,DOID:780,placenta disease,C0151864,,,MONDO:0024575,pregnancy disorder,Disorder of pregnancy | Disorder of pregnancy (disorder) | Disease of pregnancy | Disease of pregnancy (disorder)
+BMGC_DS02938,BMG_DS003883,63741006,Fungal infection of lung,,,,,,,C0151874,,,,,Fungal infection of lung | Pulmonary mycosis | Fungal infection of lung (disorder)
+BMGC_DS02939,BMG_DS003885,,,,,,,,,C0151889,,145290,MONDO:0007774,hyperreflexia,
+BMGC_DS02940,BMG_DS003888,190869004,Hypocalcemic tetany,,,,,,,C0151940,,MTHU019662,,,Hypocalcaemic tetany | Hypocalcemic tetany | Hypocalcemic tetany (disorder)
+BMGC_DS02941,BMG_DS003889,95455008,Thrombosis of cerebral veins,,,,,,,C0151945,,,,,Thrombosis of cerebral veins | Cerebral venous thrombosis | Thrombosis of cerebral veins (disorder) | Cerebral vein thrombosis
+BMGC_DS02942,BMG_DS003895,155674002;30811009,Ulcer of esophagus,,DA25.Z,"Oesophageal ulcer, unspecified",K22.1,,,C0151970,,,MONDO:0044782,esophageal ulcer,Ulcer of oesophagus | Ulcer of esophagus | Ulcer of oesophagus (disorder) | Ulcer of esophagus | Oesophageal ulcer | Esophageal ulcer | Ulcer of oesophagus | OU - Oesophageal ulcer | OU - Esophageal ulcer | Ulcer of esophagus (disorder) | Peptic ulceration of oesophagus | Peptic ulcer of oesophagus | Peptic ulceration of esophagus | Peptic ulcer of esophagus
+BMGC_DS02943,BMG_DS003896,85942002,Ulceration of intestine,,,,,,,C0151971,,,,,Ulceration of intestine | Ulceration of intestine (disorder)
+BMGC_DS02944,BMG_DS003900,,,,,,,DOID:3910,lung adenocarcinoma,C0152013,,,MONDO:0005061,lung adenocarcinoma,
+BMGC_DS02945,BMG_DS003902,,,,,,,DOID:1107,esophageal carcinoma,C0152018,,,MONDO:0019086,carcinoma of esophagus,
+BMGC_DS02946,BMG_DS003903,235675006,Gastroparesis,Gastroparesis,,,K31.84,DOID:11914,gastroparesis,C0152020,D018589,MTHU005170,MONDO:0006769,gastroparesis,Gastroparesis syndrome | Gastric atony | Gastric stasis | Gastroparesis | Gastroparesis (disorder)
+BMGC_DS02947,BMG_DS003904,,,,,,,,,C0152021,,,MONDO:0005453,congenital heart disease,
+BMGC_DS02948,BMG_DS003906,42345000;267706009;193166009;155080009,Polyneuropathy,Polyneuropathies,,,A69.22,DOID:1389,polyneuropathy,C0152025,D011115,MTHU038003,MONDO:0001824,polyneuropathy,Polyneuropathy | Acquired polyneuropathy | Polyneuropathy (disorder) | Polyneuropathy (multiple nerve disorder) | Neuropathy: [peripheral] or [polyneuropathy] | Polyneuropathy | Peripheral neuropathy | Neuropathy: [peripheral] or [polyneuropathy] (disorder) | Polyneuropathy | Polyneuropathy (disorder) | Neuropathy: [peripheral] or [polyneuropathy] | Peripheral neuropathy | Polyneuropathy | Neuropathy: [peripheral] or [polyneuropathy] (disorder)
+BMGC_DS02949,BMG_DS003907,,Retinal Vasculitis,Retinal Vasculitis,,,,DOID:11563,retinal vasculitis,C0152026,D031300,,MONDO:0006950,retinal vasculitis,
+BMGC_DS02950,BMG_DS003908,,Sensory Disorders,Sensation Disorders,,,,,,C0152027,D012678,,,,
+BMGC_DS02951,BMG_DS003910,,Borrelia recurrentis Infection,Relapsing Fever,,,,DOID:13035,louse-borne relapsing fever,C0152061,D012061,,MONDO:0001620,louse-borne relapsing fever,
+BMGC_DS02952,BMG_DS003913,47306003,Lobomycosis,Lobomycosis,1F2B,Lobomycosis,B48.0,DOID:13026,lobomycosis,C0152066,D060368,,MONDO:0001616,lobomycosis,Lobomycosis | Keloidal blastomycosis | Lobo's disease | Infection by Paracoccidioides loboii | Infection by Loboa loboii | Lobomycosis (disorder) | Cheloidal blastomycosis | Cutaneous lobomycosis | Lobomycosis infection
+BMGC_DS02953,BMG_DS003914,,tinea nigra,,,,,DOID:8912,tinea nigra,C0152067,C000656904,,MONDO:0004677,tinea nigra,
+BMGC_DS02954,BMG_DS003915,75006000,Echinococcus granulosus infection,,,,,DOID:1495,cystic echinococcosis,C0152068,,,MONDO:0044346,echinococcus granulosus infectious disease,Echinococcus granulosus infection | Unilocular hydatid disease | Echinococcus granulosus infection (disorder)
+BMGC_DS02955,BMG_DS003916,21009004,Echinococcus multilocularis infection,,,,,DOID:12148,alveolar echinococcosis,C0152069,,,MONDO:0017282,alveolar echinococcosis,Echinococcus multilocularis infection | Alveolar hydatid disease | Echinococcus multilocularis infection (disorder)
+BMGC_DS02956,BMG_DS003918,22905009,Infection by Heterophyes heterophyes,,,,,DOID:882,heterophyiasis,C0152071,,,MONDO:0004662,heterophyiasis,Infection by Heterophyes heterophyes | Heterophyiasis | Heterophyosis | Heterophyes heterophyes infection | Infection caused by Heterophyes heterophyes | Infection caused by Heterophyes heterophyes (disorder)
+BMGC_DS02957,BMG_DS003919,19341001,Ovale malaria,,,,,DOID:12919,Plasmodium ovale malaria,C0152072,,,MONDO:0001601,Plasmodium ovale malaria,Ovale malaria | Malaria by Plasmodium ovale | Ovale malaria (disorder) | Ovale tertian malaria
+BMGC_DS02958,BMG_DS003920,69163003,Taenia saginata infection,,,,,DOID:0050596,taeniasis,C0152073,,,,,Taenia saginata infection | Beef tapeworm infection | Infection by Taenia saginata | Taenia saginata infection (disorder) | Unarmed tapeworm infection | Taenia saginata taeniasis
+BMGC_DS02959,BMG_DS003922,190304001,Dyshormonogenic goiter,,,,,DOID:12175,dyshormonogenic goiter,C0152077,,,MONDO:0001460,dyshormonogenic goiter,Dyshormonogenic goitre | Dyshormonogenic goiter | Dyshormonogenic goiter (disorder)
+BMGC_DS02960,BMG_DS003923,39402007;156027002,Pelvic congestion syndrome,,,,,DOID:9346,Taylor's syndrome,C0152078,,,MONDO:0004762,Taylor syndrome,Pelvic congestion syndrome | Taylor's syndrome | Congestion-fibrosis syndrome | Pelvic congestion | Pelvic congestion syndrome (disorder) | Pelvic congestion syndrome | Pelvic congestion syndrome (disorder)
+BMGC_DS02961,BMG_DS003924,69186005,Broad ligament laceration syndrome,,,,,DOID:14133,Masters-Allen syndrome,C0152079,,,MONDO:0001887,Allen-Masters syndrome,Broad ligament laceration syndrome | Masters-Allen syndrome | Ligamentum latum laceration syndrome | Broad ligament laceration syndrome (disorder)
+BMGC_DS02962,BMG_DS003925,200973000;200901002,Pustular psoriasis,,,,,,,C0152081,,MTHU068352,MONDO:0022205,pustular psoriasis,Pustular psoriasis | Pustular psoriasis (disorder)
+BMGC_DS02963,BMG_DS003926,66191007,Transient arthropathy,,FA27,Certain specified inflammatory arthropathies,M12.8,DOID:2092,transient arthritis,C0152083,,,MONDO:0001429,transient arthropathy,Transient arthropathy | Transient arthropathy (disorder)
+BMGC_DS02964,BMG_DS003927,84801008,Jaccoud's syndrome,,,,,DOID:13080,Jaccoud's syndrome,C0152084,,,MONDO:0001629,Jaccoud syndrome,Jaccoud's syndrome | Chronic postrheumatic arthropathy | Jaccoud's arthritis | Jaccoud's disease | Chronic post - rheumatic arthropathy | Jaccoud's syndrome (disorder) | Jaccoud syndrome | Non-deforming erosive arthropathy
+BMGC_DS02965,BMG_DS003928,,,,,,,DOID:6196,reactive arthritis,C0152085,,,,,
+BMGC_DS02966,BMG_DS003930,240218006;111232005,Traumatic spondylopathy,,FA72.2,Traumatic spondylopathy,M48.3,DOID:6603,Kummell's disease,C0152088,,,MONDO:0003940,Kummell disease,Kummell's disease | Kummell's spondylitis | Kummell-Verneuil disease | Kümmell disease | Kümmell's spondylitis | Kümmell-Verneuil disease | Kümmell disease (disorder) | Traumatic spondylopathy | Traumatic spondylopathy (disorder)
+BMGC_DS02967,BMG_DS003934,267799009;200900001;5906000,Juvenile dermatitis herpetiformis,,EB42,Linear IgA bullous dermatosis,L12.2,DOID:8507,juvenile dermatitis herpetiformis,C0152092,,,MONDO:0006565,juvenile dermatitis herpetiformis,Juvenile dermatitis herpetiformis | Juvenile dermatitis herpetiformis (disorder) | Juvenile dermatitis herpetiformis | Juvenile pemphigoid | Juvenile: [dermatitis herpetiformis] or [pemphigoid] | Juvenile: [dermatitis herpetiformis] or [pemphigoid] (disorder)
+BMGC_DS02968,BMG_DS003935,85551004,Hypermobility syndrome,,LD28.1Y,Other specified types of EhlersDanlos syndrome,M35.7,DOID:13781,hypermobility syndrome,C0152093,,,MONDO:0001798,hypermobility syndrome,Hypermobility syndrome | Hypermobility syndrome (disorder) | Familial ligamentous laxity
+BMGC_DS02969,BMG_DS003936,55602000,Nezelof's syndrome,,4A01.30,Immunodeficiency due to defects of the thymus,D81.4,DOID:2012,Nezelof syndrome,C0152094,,242700,MONDO:0009451,Nezelof syndrome,Nezelof's syndrome | Congenital thymic dysplasia syndrome | Nezelof's syndrome (disorder) | Nezelof syndrome
+BMGC_DS02970,BMG_DS003937,21111006,Patau syndrome,,,,,DOID:11665,Patau syndrome,C0152095,,,MONDO:0018068,trisomy 13,Complete trisomy 13 syndrome | Patau syndrome | D>1< trisomy syndrome | Complete trisomy 13 syndrome (disorder)
+BMGC_DS02971,BMG_DS003939,48475001,Disease of diaphragm,,,,,DOID:10481,diaphragm disease,C0152097,,,MONDO:0005728,diaphragm disorder,Diaphragmatic disease | Diaphragmatic disorder | Disorder of diaphragm (disorder) | Disorder of diaphragm
+BMGC_DS02972,BMG_DS003940,,Postcholecystectomy Syndrome,Postcholecystectomy Syndrome,,,,DOID:9740,postcholecystectomy syndrome,C0152099,D017562,,MONDO:0006916,postcholecystectomy syndrome,
+BMGC_DS02973,BMG_DS003941,,Hypoplastic Left Heart Syndrome,Hypoplastic Left Heart Syndrome,,,,DOID:9955,hypoplastic left heart syndrome,C0152101,D018636,,MONDO:0004933,hypoplastic left heart syndrome,
+BMGC_DS02974,BMG_DS003942,194886003;45650007,Kyphoscoliotic heart disease,,BE2Y,Other specified diseases of the circulatory system,I27.1,DOID:12325,kyphoscoliotic heart disease,C0152102,,,MONDO:0001492,kyphoscoliotic heart disease,Kyphoscoliotic heart disease | Kyphoscoliotic heart disease (disorder)
+BMGC_DS02975,BMG_DS003943,155297007;64715009,Hypertensive heart disease,,,,I11,DOID:11516,hypertensive heart disease,C0152105,,,MONDO:0001302,hypertensive heart disease,Hypertensive heart disease | Hypertensive heart disease (disorder) | Hypertensive heart disease | Hypertensive cardiopathy | Hypertensive cardiovascular disease | Hypertensive heart disease (disorder) | HHD - hypertensive heart disease
+BMGC_DS02976,BMG_DS003944,66189004,Postmyocardial infarction syndrome,,BA60.0,Dressler syndrome,I24.1,DOID:10507,Dressler's syndrome,C0152107,,,MONDO:0001049,Dressler syndrome,Postmyocardial infarction syndrome | Post-myocardial infarction syndrome | Postmyocardial infarction syndrome (disorder)
+BMGC_DS02977,BMG_DS003945,13394002,Suberosis,,CA70.3,Suberosis,J67.3,DOID:840,cork-handlers' disease,C0152108,,,MONDO:0004549,cork-handlers' disease,Suberosis | Cork-handlers' disease | Cork-handlers' lung | Suberosis (disorder) | Cork-handlers' hypersensitivity pneumonitis
+BMGC_DS02978,BMG_DS003946,,Juvenile Spinal Muscular Atrophy,Spinal Muscular Atrophies of Childhood,,,,DOID:12376,juvenile spinal muscular atrophy,C0152109,D014897,253400,MONDO:0009672,"spinal muscular atrophy, type III",
+BMGC_DS02979,BMG_DS003948,,Foster-Kennedy Syndrome,Optic Nerve Diseases,,,,DOID:14555,Foster-Kennedy syndrome,C0152112,D009901,,MONDO:0001998,Foster-Kennedy syndrome,
+BMGC_DS02980,BMG_DS003949,,Rheumatic Chorea,Chorea,,,,,,C0152113,D002819,,MONDO:0017648,Sydenham chorea,
+BMGC_DS02981,BMG_DS003950,,Lingual-Facial-Buccal Dyskinesia,Dyskinesias,,,,DOID:9854,lingual-facial-buccal dyskinesia,C0152115,D020820,,MONDO:0004901,lingual-facial-buccal dyskinesia,
+BMGC_DS02982,BMG_DS003951,,,,,,,,,C0152116,,,MONDO:0000481,cervical dystonia,
+BMGC_DS02983,BMG_DS003953,18159001;154856000;363101005,Drug withdrawal syndrome,,,,,,,C0152128,,,,,Drug withdrawal syndrome | Drug withdrawal syndrome (disorder) | Drug withdrawal | Drug withdrawal (disorder) | Drug withdrawal syndrome
+BMGC_DS02984,BMG_DS003954,,Solar Retinitis,Foveomacular Retinitis,,,,DOID:11282,solar retinopathy,C0152131,D000099070,,,,
+BMGC_DS02985,BMG_DS003955,,Hypertensive Retinopathy,Hypertensive Retinopathy,,,,DOID:11561,hypertensive retinopathy,C0152132,D058437,,MONDO:0006797,hypertensive retinopathy,
+BMGC_DS02986,BMG_DS003956,,Internuclear Ophthalmoplegia,Ocular Motility Disorders,,,,DOID:538,internuclear ophthalmoplegia,C0152134,D015835,,MONDO:0003417,internuclear ophthalmoplegia,
+BMGC_DS02987,BMG_DS003957,69763009,Exophthalmic ophthalmoplegia,,,,,DOID:13135,exophthalmic ophthalmoplegia,C0152135,,,MONDO:0001643,exophthalmic ophthalmoplegia,Exophthalmic ophthalmoplegia | Exophthalmic ophthalmoplegia (disorder)
+BMGC_DS02988,BMG_DS003958,,Low Tension Glaucoma,Low Tension Glaucoma,,,,DOID:13544,low tension glaucoma,C0152136,D057066,,MONDO:0006837,low tension glaucoma,
+BMGC_DS02989,BMG_DS003959,32893002,Phacolytic glaucoma,,,,,DOID:12570,phacolytic glaucoma,C0152137,,,MONDO:0001553,phacolytic glaucoma,Phacolytic glaucoma | Phacolytic glaucoma (disorder)
+BMGC_DS02990,BMG_DS003960,29538005,Glaucomatocyclitic crisis,,,,,DOID:9378,glaucomatocyclitic crisis,C0152138,,,MONDO:0004772,glaucomatocyclitic crisis,Glaucomatocyclitic crisis | Posner-Schlossman syndrome | Terrien-Viel syndrome | Glaucomatocyclitic crisis (disorder)
+BMGC_DS02991,BMG_DS003962,335002,Pylorospasm,,,,,DOID:12072,pylorospasm,C0152163,,MTHU077351,MONDO:0001428,pylorospasm,Pylorospasm | Pylorospasm (disorder)
+BMGC_DS02992,BMG_DS003963,18773000,Cyclical vomiting syndrome,,,,,,,C0152164,,500007,MONDO:0010778,cyclic vomiting syndrome,Cyclical vomiting syndrome | Periodic vomiting | Cyclical vomiting | Cyclical vomiting syndrome (disorder) | Periodic vomiting syndrome
+BMGC_DS02993,BMG_DS003964,54576000;197487009;155845009,Pancreatic steatorrhea,,DC35.2,Pancreatic steatorrhoea,K90.3,DOID:10610,pancreatic steatorrhea,C0152166,,,MONDO:0001079,pancreatic steatorrhea,Pancreatic steatorrhea | Pancreatic steatorrhoea | Pancreatic steatorrhea (disorder) | Pancreatic steatorrhoea | Pancreatic steatorrhea | Pancreatic steatorrhoea (disorder)
+BMGC_DS02994,BMG_DS003965,197136003;17440005,Anal spasm,,DB72.0,Anal spasm,K59.4,DOID:11374,anal spasm,C0152167,,,MONDO:0001274,anal spasm,Anal spasm | Anal spasm (disorder)
+BMGC_DS02995,BMG_DS003967,26174007,Idiopathic pulmonary hypertension,,,,,DOID:14557,primary pulmonary hypertension,C0152171,,,MONDO:0001999,primary pulmonary hypertension,Primary pulmonary hypertension | Essential pulmonary hypertension | Primary pulmonary hypertension (disorder) | PPHT - Primary pulmonary hypertension
+BMGC_DS02996,BMG_DS003971,,Vagus Nerve Disorder,Vagus Nerve Diseases,,,,DOID:12491,Vagus nerve disease,C0152179,D020421,,MONDO:0001535,vagus nerve disorder,
+BMGC_DS02997,BMG_DS003972,,,,,,,DOID:339,accessory nerve disease,C0152180,,,MONDO:0002636,accessory nerve disorder,
+BMGC_DS02998,BMG_DS003973,,,,,,,DOID:13814,hypoglossal nerve disease,C0152181,,,MONDO:0001810,hypoglossal nerve disorder,
+BMGC_DS02999,BMG_DS003974,,,,,,,DOID:12401,intermittent explosive disorder,C0152183,,,,,
+BMGC_DS03000,BMG_DS003976,193638002,Stimulus deprivation amblyopia,,,,,DOID:10378,deprivation amblyopia,C0152189,,,MONDO:0001022,disuse amblyopia,Deprivation amblyopia | Stimulus deprivation amblyopia | Stimulus deprivation amblyopia (disorder) | Amblyopia ex anopsia | Disuse amblyopia
+BMGC_DS03001,BMG_DS003977,90927000,Refractive amblyopia,,,,H53.02,DOID:10377,refractive amblyopia,C0152190,,,MONDO:0001021,ametropic amblyopia,Refractive amblyopia | Refractive amblyopia (disorder) | Ametropic amblyopia | Meridional amblyopia
+BMGC_DS03002,BMG_DS003978,,,,,,,DOID:9335,scotoma,C0152192,,,,,
+BMGC_DS03003,BMG_DS003979,68905002,Regular astigmatism,,,,H52.22,DOID:11781,regular astigmatism,C0152193,,,MONDO:0001364,regular astigmatism,Regular astigmatism | Regular astigmatism (disorder)
+BMGC_DS03004,BMG_DS003980,47099006,Irregular astigmatism,,,,H52.21,DOID:13919,irregular astigmatism,C0152194,,,MONDO:0001831,irregular astigmatism,Irregular astigmatism | Irregular astigmatism (disorder)
+BMGC_DS03005,BMG_DS003981,30069002,Spasm of accommodation,,,,H52.53,DOID:11637,accommodative spasm,C0152196,,,MONDO:0001329,accommodative spasm,Spasm of accommodation | Spasm of accommodation (disorder) | Ciliary muscle spasm
+BMGC_DS03006,BMG_DS003982,86266009;193630009,Total internal ophthalmoplegia,,,,,DOID:11177,total internal ophthalmoplegia,C0152197,,,MONDO:0001211,total internal ophthalmoplegia,Total internal ophthalmoplegia | Complete internal ophthalmoplegia | Total internal ophthalmoplegia (disorder) | Total internal ophthalmoplegia | Total internal ophthalmoplegia (disorder)
+BMGC_DS03007,BMG_DS003983,155137002;54552008,Disorder of accommodation,,,,,DOID:10034,eye accommodation disease,C0152198,,,MONDO:0000926,eye accommodation disease,Disorder of accommodation | Disorder of accommodation (disorder)
+BMGC_DS03008,BMG_DS003984,56852002,Achromatopsia,Color Vision Defects,,,H53.51,DOID:13911,achromatopsia,C0152200,D003117,,MONDO:0018852,achromatopsia,Achromatopsia | Monochromatism | Achromatism | Achromatopsia (disorder)
+BMGC_DS03009,BMG_DS003985,,,,,,,DOID:11491,acquired night blindness,C0152202,,,MONDO:0001296,acquired night blindness,
+BMGC_DS03010,BMG_DS003986,,"Strabismus, Comitant",Strabismus,,,,,,C0152203,D013285,,,,
+BMGC_DS03011,BMG_DS003987,,Monocular Esotropia,Esotropia,,,,DOID:10293,monocular esotropia,C0152204,D004948,,MONDO:0000997,monocular esotropia,
+BMGC_DS03012,BMG_DS003988,39837002;194080005,Alternating esotropia,,,,H50.05,DOID:9888,alternating esotropia,C0152205,,MTHU068693,MONDO:0004913,alternating esotropia,Alternating esotropia | Alternating esotropia (disorder)
+BMGC_DS03013,BMG_DS003989,,Monocular Exotropia,Exotropia,,,,DOID:11853,monocular exotropia,C0152206,D005099,,MONDO:0001392,monocular exotropia,
+BMGC_DS03014,BMG_DS003990,,Alternating Exotropia,Exotropia,,,,DOID:1142,alternating exotropia,C0152207,D005099,,MONDO:0001281,alternating exotropia,
+BMGC_DS03015,BMG_DS003991,29491004,Hypotropia,,,,,DOID:9841,hypotropia,C0152208,,MTHU062617,MONDO:0004897,hypotropia,Hypotropia | Hypotropia (disorder) | hyop - Hypotropia
+BMGC_DS03016,BMG_DS003992,,cyclotropia,,,,,DOID:9838,cyclotropia,C0152209,C000721272,,MONDO:0004894,cyclotropia,
+BMGC_DS03017,BMG_DS003993,74025007,Intermittent tropia,,,,,DOID:1942,intermittent squint,C0152210,,,MONDO:0002152,intermittent squint,Intermittent squint | Intermittent tropia | Intermittent tropia (disorder)
+BMGC_DS03018,BMG_DS003998,267745004;155196009;62176008,Esophoria,Esotropia,,,H50.51,,,C0152216,D004948,MTHU037173,,,(Esophoria) or (strabismus NOS) or (ophthalmoplegia NOS) | Strabismus NOS | Esophoria | Ophthalmoplegia NOS | (Esophoria) or (strabismus NOS) or (ophthalmoplegia NOS) (disorder) | (Esophoria) or (strabismus NOS) or (ophthalmoplegia NOS) | Ophthalmoplegia NOS | Esophoria | Strabismus NOS | (Esophoria) or (strabismus NOS) or (ophthalmoplegia NOS) (disorder) | Esophoria | Esophoria (disorder) | Latent convergent squint
+BMGC_DS03019,BMG_DS004001,60017001,Cyclophoria,Ocular Motility Disorders,,,H50.54,,,C0152219,D015835,,,,Cyclophoria | Cyclophoria (disorder)
+BMGC_DS03020,BMG_DS004003,12942001;400942002,Paralytic strabismus,,,,H49,DOID:10863,paralytic squint,C0152221,,,MONDO:0001143,paralytic strabismus,Paralytic squint | Incomitant dissociation | Non-comitant strabismus | Incomitant dissociation (disorder) | Paralytic strabismus (disorder) | Paralytic strabismus | Paralytic squint
+BMGC_DS03021,BMG_DS004004,,Parinaud Syndrome,Ocular Motility Disorders,,,,,,C0152222,D015835,,MONDO:0022220,Parinaud syndrome,
+BMGC_DS03022,BMG_DS004005,,Mechanical Strabismus,Strabismus,,,,DOID:9306,mechanical strabismus,C0152223,D013285,,MONDO:0004753,mechanical strabismus,
+BMGC_DS03023,BMG_DS004008,60735000;193936001,Lagophthalmos,Lagophthalmos,9A03.4Z,"Lagophthalmos, unspecified",H02.2,DOID:12959,lagophthalmos,C0152226,D000092164,MTHU036832,MONDO:0001604,lagophthalmos,Lagophthalmos | Defective lid closure | Poor closure eyelids | Lagophthalmos (finding) | Lagophthalmos | Lagophthalmos (disorder)
+BMGC_DS03024,BMG_DS004009,49393005,Excessive tearing,,,,,DOID:13757,excessive tearing,C0152227,,MTHU075796,MONDO:0001793,excessive tearing,Excessive tearing | Watery eyes | Illacrimation | Excessive tear production | Watering eye | Crocodile tears | Excessive tear production (disorder) | Tearing eyes
+BMGC_DS03025,BMG_DS004015,,,,,,,,,C0152240,,,MONDO:0015839,septate uterus,
+BMGC_DS03026,BMG_DS004016,,,,,,,DOID:10686,lactocele,C0152243,,,MONDO:0001099,lactocele,
+BMGC_DS03027,BMG_DS004019,201210008;23894009,Acne varioliformis,,ED81.Y,Other specified acneform inflammatory disorders,L70.2,DOID:6543,acne,C0152249,,,,,Acne varioliformis | Acne varioliformis (disorder) | Acne varioliformis | Acne frontalis | Acne varioliformis (disorder)
+BMGC_DS03028,BMG_DS004020,155491005;155456002;31268005,Thrombophlebitis migrans,,BD70.2,Thrombophlebitis migrans,I82.1,DOID:14392,thrombophlebitis migrans,C0152250,,,MONDO:0001954,thrombophlebitis migrans,Thrombophlebitis migrans | Thrombophlebitis migrans (disorder) | Thrombophlebitis migrans | Trousseau's syndrome | Migratory thrombophlebitis | Thrombophlebitis migrans (disorder)
+BMGC_DS03029,BMG_DS004023,111512005,Posterior synechiae,,,,,,,C0152253,,MTHU073515,,,Posterior synechiae | Posterior synechiae (disorder)
+BMGC_DS03030,BMG_DS004024,267735001;87614000;155169006,Pinguecula,Pinguecula,,,H11.15,DOID:11029,pinguecula,C0152255,D059407,,MONDO:0001179,pinguecula,Pinguecula | Chemosis of conjunctiva | Disorders of conjunctiva NOS | Symblepharon | (Disorders of conjunctiva NOS) or (chemosis) or (pinguecula) or (symblepharon) | (Disorders of conjunctiva NOS) or (chemosis) or (pinguecula) or (symblepharon) (disorder) | Pinguecula | Pinguicula | Pinguecula (disorder) | (Disorders of conjunctiva NOS) or (chemosis) or (pinguecula) or (symblepharon) | Pinguecula | Symblepharon | Disorders of conjunctiva NOS | Chemosis of conjunctiva | (Disorders of conjunctiva NOS) or (chemosis) or (pinguecula) or (symblepharon) (disorder)
+BMGC_DS03031,BMG_DS004026,,,,,,,DOID:13717,mature cataract,C0152257,,,,,
+BMGC_DS03032,BMG_DS004027,247065006;264443002,Morgagnian cataract,,,,,DOID:13964,Morgagni cataract,C0152258,,,MONDO:0001848,Morgagni cataract,Morgagnian cataract | Morgagnian cataract (finding) | Morgagnian cataract (disorder) | Morgagnian cataract
+BMGC_DS03033,BMG_DS004029,13285005,Cystitis cystica,,,,,DOID:7138,cystitis cystica,C0152262,,,MONDO:0004118,cystitis cystica,Cystitis cystica | Cystitis cystica (disorder)
+BMGC_DS03034,BMG_DS004031,17342003;267571003;154840005,Familial erythrocytosis,,3A80.0,Primary inherited erythrocytosis,D75.0,DOID:10780;DOID:0060652,primary polycythemia | familial erythrocytosis 1,C0152264,,,MONDO:0001115,familial polycythemia,Hereditary pure erythrocytosis | Familial polycythemia | Familial erythrocytosis | Familial polycythaemia | Familial erythrocytosis (disorder) | (Other blood diseases) or (familial erythrocytosis) or (hypergammaglobulinemia) | Familial erythrocytosis | Other blood diseases | Erythrocytosis - familial | Hypergammaglobulinaemia | (Other blood diseases) or (familial erythrocytosis) or (hypergammaglobulinaemia) | Hypergammaglobulinemia | (Other blood diseases) or (familial erythrocytosis) or (hypergammaglobulinaemia) (disorder) | (Other blood diseases) or (familial erythrocytosis) or (hypergammaglobulinemia) | Erythrocytosis - familial | Other blood diseases | Familial erythrocytosis | (Other blood diseases) or (familial erythrocytosis) or (hypergammaglobulinaemia) | Hypergammaglobulinaemia | Hypergammaglobulinemia | (Other blood diseases) or (familial erythrocytosis) or (hypergammaglobulinaemia) (disorder)
+BMGC_DS03035,BMG_DS004032,,,,,,,DOID:8654,"Hodgkin's lymphoma, mixed cellularity",C0152266,,,MONDO:0004633,"Hodgkin's lymphoma, mixed cellularity",
+BMGC_DS03036,BMG_DS004033,,,,,,,DOID:8628,"Hodgkin's lymphoma, lymphocytic depletion",C0152267,,,MONDO:0004620,"Hodgkin's lymphoma, lymphocytic depletion",
+BMGC_DS03037,BMG_DS004034,,,,,,,DOID:8838,"Hodgkin's lymphoma, nodular sclerosis",C0152268,,,MONDO:0004665,nodular sclerosis classical Hodgkin lymphoma,
+BMGC_DS03038,BMG_DS004035,,,,,,,DOID:8997,polycythemia vera,C0152272,,,,,
+BMGC_DS03039,BMG_DS004036,,,,,,,DOID:8696,subacute monocytic leukemia,C0152275,,,MONDO:0004644,subacute monocytic leukemia,
+BMGC_DS03040,BMG_DS004037,,,,,,,DOID:8683,myeloid sarcoma,C0152276,,,MONDO:0006237,granulocytic sarcoma,
+BMGC_DS03041,BMG_DS004039,,,,,,,,,C0152415,,106280,MONDO:0007125,ankyloglossia,
+BMGC_DS03042,BMG_DS004040,,,,,,,DOID:1712,aortic valve stenosis,C0152417,,,MONDO:0017735,congenital aortic valve stenosis,
+BMGC_DS03043,BMG_DS004041,,,,,,,,,C0152419,,,MONDO:0009010,aortic arch interruption,
+BMGC_DS03044,BMG_DS004042,,,,,,,DOID:11367,congenital aphakia,C0152422,,,,,
+BMGC_DS03045,BMG_DS004043,,,,,,,,,C0152426,,,MONDO:0018969,craniorachischisis,
+BMGC_DS03046,BMG_DS004044,,,,,,,DOID:1148,polydactyly,C0152427,,603596,MONDO:0021003,polydactyly,
+BMGC_DS03047,BMG_DS004047,,,,,,,,,C0152438,,184400,MONDO:0008482,Sprengel deformity,
+BMGC_DS03048,BMG_DS004048,44268007;389992006,Retinoschisis,Retinoschisis,,,,DOID:8465,retinoschisis,C0152439,D041441,MTHU006950,MONDO:0004579,retinoschisis,Retinoschisis | Schisis of retina | RS - Retinoschisis | Retinoschisis (disorder) | Retinoschisis | Retinoschisis (disorder)
+BMGC_DS03049,BMG_DS004049,193849005;52476003,Corneal staphyloma,,,,H18.72,DOID:12753,corneal staphyloma,C0152440,,,MONDO:0001579,corneal staphyloma,Corneal staphyloma | Corneal staphyloma (disorder)
+BMGC_DS03050,BMG_DS004052,90531003,Urethral diverticulum,,GC06,Urethral diverticulum,N36.1,DOID:9341,urethral diverticulum,C0152443,,,,,Urethral diverticulum | Urethral diverticulum (disorder)
+BMGC_DS03051,BMG_DS004054,197421008;47312008,Hydrops of gallbladder,,DC10.1,Hydrops of gallbladder,K82.1,DOID:9717,hydrops of gallbladder,C0152445,,,MONDO:0004859,hydrops of gallbladder,(Mucocele of gallbladder) or (hydrops of gallbladder) | Mucocele of gallbladder | Hydrops of gallbladder | Hydrops of gallbladder | Hydrops of gallbladder (disorder)
+BMGC_DS03052,BMG_DS004056,197612003;266614002;155852006;20917003,Chronic glomerulonephritis,,,,,,,C0152451,,,,,Chronic nephropathy (& [glomerulonephritis] or [nephritis]) | Nephritis - chronic | Nephropathy - chronic | Chronic glomerulonephritis | Chronic nephropathy (& [glomerulonephritis] or [nephritis]) (disorder) | (Chronic glomerulonephritis) or (nephritis - chronic) | Chronic glomerulonephritis | Nephritis - chronic | Glomeruloneph.- chronic | (Chronic glomerulonephritis) or (nephritis - chronic) (disorder) | (Chronic glomerulonephritis) or (nephritis - chronic) | Glomeruloneph.- chronic | Nephritis - chronic | Chronic glomerulonephritis | (Chronic glomerulonephritis) or (nephritis - chronic) (disorder) | Chronic glomerulonephritis | Chronic glomerulonephritis (disorder) | CGN - Chronic glomerulonephritis
+BMGC_DS03053,BMG_DS004057,37715009;194965002,Fibrosis of pericardium,,,,,,,C0152452,,,,,Adhesive pericarditis | Adherent pericardium | Adhesive pericarditis (disorder) | Fibrosis of pericardium | Fibrosis of pericardium (disorder)
+BMGC_DS03054,BMG_DS004059,85149007,Keratomalacia,,,,H18.44,DOID:11267,keratomalacia,C0152455,C536156,,MONDO:0001250,keratomalacia,Keratomalacia | Keratomalacia (disorder)
+BMGC_DS03055,BMG_DS004060,61565001,Cholesterolosis of gallbladder,,DC10.4,Cholesterolosis of gallbladder,K82.4,DOID:10254,strawberry gallbladder,C0152456,,,MONDO:0000987,cholesterolosis of gallbladder,Cholesterolosis of gallbladder | Strawberry gallbladder | Cholesterolosis of gallbladder (disorder) | Gallbladder cholesterolosis
+BMGC_DS03056,BMG_DS004061,77103006,Kayser-Fleischer ring,,,,H18.04,,,C0152457,,MTHU038006,,,Kayser-Fleischer ring | Kayser-Fleischer ring (disorder)
+BMGC_DS03057,BMG_DS004062,193288000;1361009,Leukocoria,,,,,DOID:11772,leukocoria,C0152458,,MTHU009657,,,Leukocoria | Leukocoria (disorder) | Leukocoria | Leukocoria (disorder) | Leucocoria
+BMGC_DS03058,BMG_DS004063,198028006;367113004;198033005;43790000,Balanitis xerotica obliterans,,,,,DOID:13477,balanitis xerotica obliterans,C0152460,,,MONDO:0001725,balanitis xerotica obliterans,Peyronie's disease | Balanitis xerotica obliterans | (Peyronie's disease) or (balanitis xerotica obliterans) | (Peyronie's disease) or (balanitis xerotica obliterans) (disorder) | Balanitis xerotica obliterans | Balanitis xerotica obliterans (disorder) | Balanitis xerotica obliterans | BXO - Balanitis xerotica obliterans | Balanitis xerotica obliterans (disorder) | Lichen sclerosus of glans penis | Lichen sclerosus et atrophicus of glans penis AND prepuce | Lichen sclerosus et atrophicus of glans penis AND prepuce (disorder)
+BMGC_DS03059,BMG_DS004065,,Salmonella sepsis,,1C41,Bacterial infection of unspecified site,A02.1,,,C0152486,,,,,
+BMGC_DS03060,BMG_DS004072,39224005,Acute amebiasis,,1A36.00,Acute amoebiasis,A06.0,,,C0152499,,,,,Acute amebiasis | Acute amoebiasis | Acute amebiasis (disorder)
+BMGC_DS03061,BMG_DS004073,23874000;186117001,Chronic intestinal amebiasis,,1A36.0Z,"Intestinal infections due to Entamoeba, unspecified",A06.1,,,C0152500,,,,,Chronic amebiasis | Chronic amebic dysentery | Chronic amoebic dysentery | Chronic amoebiasis | Chronic amebiasis (disorder) | Chronic intestinal amebiasis | Chronic intestinal amoebiasis | Chronic intestinal amebiasis | Chronic intestinal amoebiasis | Chronic intestinal amebiasis (disorder)
+BMGC_DS03062,BMG_DS004079,186127007,Other specified protozoal intestinal diseases,,1A3Z,"Protozoal intestinal infections, unspecified",A07.8,DOID:14397,protozoal dysentery,C0152507,,,,,Other specified protozoal intestinal diseases | Other specified protozoal intestinal diseases (disorder)
+BMGC_DS03063,BMG_DS004080,82930004,Intestinal infection caused by Pseudomonas,,,,,,,C0152515,,,,,Intestinal infection caused by Pseudomonas | Intestinal infection caused by Pseudomonas (disorder)
+BMGC_DS03064,BMG_DS004081,75375008,Bacterial enteritis,,,,,,,C0152516,,,,,Bacterial enteritis | Septic enteritis | Bacterial enteritis of intestine | Inflammation of intestine caused by bacteria | Inflammation of intestine caused by bacteria (disorder)
+BMGC_DS03065,BMG_DS004082,266178009;154277007;186166004;66550001;111843007,Viral gastroenteritis,,,,,,,C0152517,,,,,Viral: [ill-defined GIT infections (& diarrhea)] or [gastroenteritis] | Viral + ill-defined GIT inf. | Gastroent. - viral | Viral and ill-defined gastrointestinal infections | Viral gastroenteritis | Diarrhoea-viral GIT inf | Diarrhea-viral GIT inf | Viral: [ill-defined GIT infections (& diarrhoea)] or [gastroenteritis] | Viral: [ill-defined GIT infections (& diarrhoea)] or [gastroenteritis] (disorder) | Viral: [ill-defined GIT infections (& diarrhea)] or [gastroenteritis] | Viral gastroenteritis | Viral + ill-defined GIT inf. | Gastroent. - viral | Viral and ill-defined gastrointestinal infections | Viral: [ill-defined GIT infections (& diarrhoea)] or [gastroenteritis] | Diarrhoea-viral GIT inf | Diarrhea-viral GIT inf | Viral: [ill-defined GIT infections (& diarrhoea)] or [gastroenteritis] (disorder) | (Epidemic diarrhoea) or (viral gastroenteritis) | (Epidemic diarrhea) or (viral gastroenteritis) | Viral gastroenteritis | Epidemic diarrhea | Epidemic diarrhoea | (Epidemic diarrhoea) or (viral gastroenteritis) (disorder) | Nonbacterial gastroenteritis | Nonbacterial gastroenteritis (disorder) | Viral gastroenteritis | Viral diarrhea | Viral vomiting | Viral diarrhoea | Viral gastroenteritis (disorder)
+BMGC_DS03066,BMG_DS004086,186172004,Tuberculous pleurisy in primary progressive tuberculosis,,,,,DOID:106,pleural tuberculosis,C0152531,,,,,Tuberculous pleurisy in primary progressive tuberculosis | Tuberculous pleurisy in primary progressive tuberculosis (disorder) | Primary progressive tuberculosis with tuberculous pleurisy
+BMGC_DS03067,BMG_DS004094,29731002,Tuberculous pneumothorax,,1B10.0,"Respiratory tuberculosis, confirmed",A15.0,DOID:9534,tuberculous pneumothorax,C0152600,,,MONDO:0004813,tuberculous pneumothorax,Tuberculous pneumothorax | Tuberculous pneumothorax (disorder)
+BMGC_DS03068,BMG_DS004102,,,,,,,DOID:13282,intestinal tuberculosis,C0152724,,,,,
+BMGC_DS03069,BMG_DS004107,32268008,Tuberculosis of urinary bladder,,,,,DOID:754,bladder tuberculosis,C0152793,,,MONDO:0004272,urinary bladder tuberculosis,Tuberculosis of bladder | Tuberculosis of urinary bladder (disorder) | Tuberculosis of urinary bladder | TB (tuberculosis) of urinary bladder
+BMGC_DS03070,BMG_DS004108,81359005,Tuberculosis of ureter,,,,,DOID:827,ureter tuberculosis,C0152800,,,MONDO:0004517,ureter tuberculosis,Tuberculosis of ureter | Tuberculosis of ureter (disorder) | TB - Tuberculosis of ureter
+BMGC_DS03071,BMG_DS004109,83652003,Tuberculosis of epididymis,,,,,DOID:1251,tuberculous epididymitis,C0152814,,,MONDO:0001537,tuberculous epididymitis,Tuberculosis of epididymis | Tuberculous epididymitis | Tuberculosis of epididymis (disorder)
+BMGC_DS03072,BMG_DS004111,,Tuberculous oophoritis and salpingitis,,,,A18.17,DOID:2148;DOID:0050166,tuberculous salpingitis | tuberculous oophoritis,C0152828,,,,,
+BMGC_DS03073,BMG_DS004114,186269001,Tuberculosis of ear,,,,,,,C0152874,,,,,Tuberculosis of ear | Tuberculosis of ear (disorder)
+BMGC_DS03074,BMG_DS004117,15284007,Tuberculosis of esophagus,,,,,DOID:7332,esophageal tuberculosis,C0152902,,,MONDO:0004189,esophageal tuberculosis,Tuberculosis of esophagus | Tuberculosis of oesophagus | Tuberculosis of esophagus (disorder)
+BMGC_DS03075,BMG_DS004120,,Septicemic Plague,Plague,,,,DOID:3481,septicemic plague,C0152936,D010930,,MONDO:0005956,septicemic plague,
+BMGC_DS03076,BMG_DS004121,35339003,Primary pneumonic plague,,,,,DOID:10398,pneumonic plague,C0152937,,,,,Primary pneumonic plague | Primary pneumonic plague (disorder)
+BMGC_DS03077,BMG_DS004122,67525007,Secondary pneumonic plague,,,,,DOID:10398,pneumonic plague,C0152938,,,,,Secondary pneumonic plague | Secondary pneumonic plague (disorder)
+BMGC_DS03078,BMG_DS004123,37722001,Ulceroglandular tularemia,,1B94.0,Ulceroglandular tularaemia,A21.0,DOID:11990,ulceroglandular tularemia,C0152941,,,MONDO:0001413,ulceroglandular tularemia,Ulceroglandular tularemia | Ulceroglandular tularaemia | Ulceroglandular tularemia (disorder)
+BMGC_DS03079,BMG_DS004124,186292001;398599000;62769007,Enteric tularemia,,,,,DOID:14239,gastrointestinal tularemia,C0152942,,,,,Enteric tularemia | Intestinal tularemia | Typhoidal tularaemia | Enteric tularaemia | Intestinal tularaemia | Typhoidal tularemia | Typhoidal tularemia (disorder) | Enteric tularemia (disorder) | Enteric tularaemia | Enteric tularemia | Intestinal tularaemia | Intestinal tularemia | Enteric tularemia | Cryptogenic tularemia | Intestinal tularemia | Typhoidal tularemia | Oropharyngeal tularemia | Oropharyngeal tularaemia | Typhoidal tularaemia | Enteric tularaemia | Intestinal tularaemia | Cryptogenic tularaemia | Enteric tularemia (disorder)
+BMGC_DS03080,BMG_DS004125,73363000,Oculoglandular tularemia,,1B94.Y,Other specified tularaemia,A21.1,DOID:13226,oculoglandular tularemia,C0152944,,,MONDO:0001665,oculoglandular tularemia,Oculoglandular tularemia | Oculoglandular tularaemia | Oculoglandular tularemia (disorder)
+BMGC_DS03081,BMG_DS004126,186302005;111798006,Gastrointestinal anthrax,,1B97,Anthrax,A22.2,DOID:13386,gastrointestinal anthrax,C0152945,C571911,,MONDO:0001701,gastrointestinal anthrax,Gastrointestinal anthrax | Gastrointestinal anthrax (disorder)
+BMGC_DS03082,BMG_DS004127,,Anthrax sepsis,,1B97,Anthrax,A22.7,,,C0152946,,,,,
+BMGC_DS03083,BMG_DS004129,26117009,Diphtheritic myocarditis,,,,A36.81,,,C0152952,,,MONDO:0041259,diphtheritic myocarditis,Diphtheritic myocarditis | Diphtheritic myocarditis (disorder)
+BMGC_DS03084,BMG_DS004130,13596001,Diphtheritic peritonitis,,,,A36.89,DOID:13310,diphtheritic peritonitis,C0152953,,,MONDO:0001682,diphtheritic peritonitis,Diphtheritic peritonitis | Diphtheritic peritonitis (disorder)
+BMGC_DS03085,BMG_DS004131,197847008;48278001,Diphtheritic cystitis,,,,A36.85,DOID:13306,diphtheritic cystitis,C0152954,,,MONDO:0001681,diphtheritic cystitis,Diphtheritic cystitis | Diphtheritic cystitis (disorder) | Diphtheritic cystitis | Diphtheritic cystitis (disorder) | Cystitis in diphtheria
+BMGC_DS03086,BMG_DS004138,,Streptococcal sepsis,,,,A40,,,C0152964,,,,,
+BMGC_DS03087,BMG_DS004140,1976008,Septicemia due to anaerobes,,,,,,,C0152967,,,,,Anaerobic septicemia | Anaerobic septicaemia | Anaerobic septicemia (disorder) | Septicaemia due to anaerobes | Septicemia due to anaerobes
+BMGC_DS03088,BMG_DS004143,14535005,Acute nonparalytic poliomyelitis,,1C81,Acute poliomyelitis,A80.4,DOID:4986,nonparalytic poliomyelitis,C0152998,,,MONDO:0003231,acute nonparalytic poliomyelitis,"Acute nonparalytic poliomyelitis | Anterior acute poliomyelitis specified as nonparalytic | Epidemic acute poliomyelitis specified as non paralytic | Anterior acute poliomyelitis, nonparalytic | Epidemic acute poliomyelitis, non paralytic | Acute nonparalytic poliomyelitis (disorder) | Acute non-paralytic poliomyelitis"
+BMGC_DS03089,BMG_DS004153,42448002,Herpes zoster keratoconjunctivitis,,,,B02.33,,,C0153027,,,,,Herpes zoster keratoconjunctivitis | Herpes zoster keratoconjunctivitis (disorder) | Herpes zoster with keratoconjunctivitis
+BMGC_DS03090,BMG_DS004158,186544000,Herpes simplex eyelid dermatitis,,,,,DOID:9123,eczema herpeticum,C0153037,,,,,Herpes simplex eyelid dermatitis | Herpes simplex eyelid dermatitis (disorder) | Herpes simplex dermatitis of eyelid
+BMGC_DS03091,BMG_DS004161,43891009,Herpetic whitlow,,,,,DOID:8607,herpetic whitlow,C0153042,,,MONDO:0004616,herpetic whitlow,Herpetic whitlow | Herpetic felon | Herpes simplex whitlow | Herpetic whitlow (disorder)
+BMGC_DS03092,BMG_DS004176,,"Encephalomyelitis, Western Equine","Encephalomyelitis, Western Equine",,,,DOID:10843,Western equine encephalitis,C0153064,D020241,,MONDO:0019380,western equine encephalitis,
+BMGC_DS03093,BMG_DS004177,,"Encephalomyelitis, Eastern Equine","Encephalomyelitis, Eastern Equine",,,,DOID:10841,Eastern equine encephalitis,C0153065,D020242,,MONDO:0005736,eastern equine encephalitis,
+BMGC_DS03094,BMG_DS004178,66454007,Murray valley encephalitis,,,,,DOID:10842,Murray Valley encephalitis,C0153066,,,MONDO:0001137,Murray valley encephalitis,Australian encephalitis | Australian arboencephalitis | Australian X disease | MVE - Murray Valley encephalitis | Murray River encephalitis | Murray Valley encephalitis | Murray Valley encephalitis (disorder)
+BMGC_DS03095,BMG_DS004201,29976007,"Trachoma, initial stage",,,,,DOID:11265,trachoma,C0153107,,,,,"Trachoma, initial stage | Trachoma dubium | Trachoma dubium - initial stage | Trachoma, initial stage (disorder)"
+BMGC_DS03096,BMG_DS004202,52812002,"Trachoma, active stage",,,,,DOID:11265,trachoma,C0153108,,,,,"Trachoma, active stage | Trachoma, active stage (disorder)"
+BMGC_DS03097,BMG_DS004205,,Acute Peripheral Vestibulopathy,Vestibular Neuronitis,,,,,,C0153113,D020338,,,,
+BMGC_DS03098,BMG_DS004211,21070001,Mixed malaria,,,,,DOID:14325,mixed malaria,C0153121,,,MONDO:0001944,mixed malaria,Mixed malaria | Malaria by more than one parasite | Mixed malaria (disorder)
+BMGC_DS03099,BMG_DS004217,,"Neurosyphilis, Juvenile",Neurosyphilis,,,,DOID:10039,late congenital syphilis,C0153132,D009494,,,,
+BMGC_DS03100,BMG_DS004220,,,,,,,DOID:10039,late congenital syphilis,C0153136,,,,,
+BMGC_DS03101,BMG_DS004221,186846005,Early symptomatic syphilis,,,,,DOID:4156,primary syphilis,C0153139,,,,,Early symptomatic syphilis | Early symptomatic syphilis (disorder)
+BMGC_DS03102,BMG_DS004238,,Syphilitic aseptic meningitis,,,,,DOID:10073,syphilitic meningitis,C0153166,C536775,,MONDO:0000936,syphilitic meningitis,
+BMGC_DS03103,BMG_DS004239,,"Neurosyphilis, Asymptomatic",Neurosyphilis,,,,DOID:10035,asymptomatic neurosyphilis,C0153167,D009494,,MONDO:0000927,asymptomatic neurosyphilis,
+BMGC_DS03104,BMG_DS004240,26135000,Syphilitic encephalitis,,,,,DOID:10081,syphilitic encephalitis,C0153168,,,MONDO:0000937,syphilitic encephalitis,Syphilitic encephalitis | Syphilitic encephalitis (disorder)
+BMGC_DS03105,BMG_DS004255,,"Syphilis, tertiary",,,,,DOID:8200,tertiary syphilis,C0153188,C536774,,MONDO:0004497,tertiary syphilis,
+BMGC_DS03106,BMG_DS004256,24868007,Acute gonococcal cystitis,,,,,DOID:13690,acute gonococcal cystitis,C0153191,,,MONDO:0001777,acute gonococcal cystitis,Acute gonococcal cystitis | Acute gonococcal cystitis (disorder) | Bladder gonorrhoea - acute | Bladder gonorrhea - acute
+BMGC_DS03107,BMG_DS004257,111806005,Acute gonococcal prostatitis,,,,,DOID:13943,acute gonococcal prostatitis,C0153192,,,MONDO:0001838,acute gonococcal prostatitis,Acute gonococcal prostatitis | Acute gonococcal prostatitis (disorder)
+BMGC_DS03108,BMG_DS004258,30168008;186912008,Acute gonococcal epididymo-orchitis,,,,,DOID:10802,acute gonococcal epididymo-orchitis,C0153193,,,MONDO:0001125,acute gonococcal epididymo-orchitis,Acute gonococcal epididymo-orchitis | Acute gonococcal epididymo-orchitis (disorder) | Acute gonococcal: [epididymo-orchitis] or [orchitis] | Acute gonococcal orchitis | Acute gonococcal epididymo-orchitis | Acute gonococcal: [epididymo-orchitis] or [orchitis] (disorder)
+BMGC_DS03109,BMG_DS004260,20943002,Acute gonococcal cervicitis,,,,,DOID:10615,acute gonococcal cervicitis,C0153195,,,MONDO:0001080,acute gonococcal cervicitis,Acute gonococcal cervicitis | Acute inflammation of cervix uteri caused by Neisseria gonorrhoeae (disorder) | Acute inflammation of cervix uteri caused by Neisseria gonorrhoeae
+BMGC_DS03110,BMG_DS004261,186913003;65295003,Acute gonococcal endometritis,,,,,DOID:7527,acute gonococcal endometritis,C0153196,,,MONDO:0004264,acute gonococcal endometritis,Uterus - acute gonorrhea | Acute gonococcal endometritis | Uterus - acute gonorrhoea | Acute gonococcal endometritis (disorder) | Acute gonococcal endometritis | Uterus - acute gonorrhoea | Uterus - acute gonorrhea | Acute gonococcal endometritis (disorder)
+BMGC_DS03111,BMG_DS004265,23975003,Chronic gonococcal seminal vesiculitis,,,,,DOID:10399,seminal vesicle chronic gonorrhea,C0153205,,,MONDO:0001025,seminal vesicle chronic gonorrhea,Chronic gonococcal seminal vesiculitis | Chronic gonococcal seminal vesiculitis (disorder)
+BMGC_DS03112,BMG_DS004266,76802005,Chronic gonococcal cervicitis,,,,,DOID:1512,chronic gonorrhea of cervix,C0153206,,,MONDO:0002029,chronic gonorrhea of cervix,Chronic gonococcal cervicitis | Chronic inflammation of cervix uteri caused by Neisseria gonorrhoeae (disorder) | Chronic inflammation of cervix uteri caused by Neisseria gonorrhoeae
+BMGC_DS03113,BMG_DS004268,53529004,Chronic gonococcal salpingitis,,,,,DOID:12718,chronic gonococcal salpingitis,C0153208,,,MONDO:0001575,chronic gonococcal salpingitis,Chronic gonococcal salpingitis | Chronic gonococcal salpingitis (disorder)
+BMGC_DS03114,BMG_DS004270,186922002;9091006,Gonococcal iridocyclitis,,,,A54.32,DOID:9384,gonococcal iridocyclitis,C0153212,,,MONDO:0004774,gonococcal iridocyclitis,Gonococcal iridocyclitis | Gonococcal iridocyclitis (disorder)
+BMGC_DS03115,BMG_DS004271,186923007;111807001,Gonococcal endophthalmia,,,,A54.39,DOID:9698,gonococcal endophthalmia,C0153213,,,MONDO:0004853,gonococcal endophthalmia,Gonococcal endophthalmia | Gonococcal endophthalmia (disorder)
+BMGC_DS03116,BMG_DS004272,186924001;40149008,Gonococcal keratitis,,,,A54.33,DOID:9697,gonococcal keratitis,C0153214,,,MONDO:0004852,gonococcal keratitis,Gonococcal keratitis | Gonococcal keratitis (disorder) | Gonococcal keratitis | Keratitis blennorrhagica | Gonococcal keratitis (disorder)
+BMGC_DS03117,BMG_DS004274,44743006,Gonococcal joint infection,,,,,,,C0153216,,,MONDO:0041903,gonococcal infection of joint,Gonococcal infection of joint | Gonococcal arthritis | Gonococcal rheumatism | Gonococcal joint infection | Gonococcal infection of joint (disorder)
+BMGC_DS03118,BMG_DS004275,186928003;46699001,Gonococcal bursitis,,,,A54.49,DOID:13453,gonococcal bursitis,C0153218,,,MONDO:0001719,gonococcal bursitis,Gonococcal bursitis | Gonococcal bursitis (disorder) | Gonococcal bursitis | Bursitis caused by Neisseria gonorrhoeae (disorder) | Bursitis caused by Neisseria gonorrhoeae
+BMGC_DS03119,BMG_DS004276,186929006;53664003,Gonococcal spondylitis,,,,,DOID:13127,gonococcal spondylitis,C0153219,,,MONDO:0001640,gonococcal spondylitis,Gonococcal spondylitis | Gonococcal spondylitis (disorder)
+BMGC_DS03120,BMG_DS004279,151004;186935006,Gonococcal meningitis,,,,A54.81,,,C0153225,,,,,Gonococcal meningitis | Gonococcal meningitis (disorder) | Meningitis due to gonococcus | Gonococcal meningitis | Gonococcal meningitis (disorder)
+BMGC_DS03121,BMG_DS004281,186937003;61048000,Gonococcal endocarditis,,,,A54.83,,,C0153227,,,,,Gonococcal endocarditis | Gonococcal endocarditis (disorder) | Gonococcal endocarditis | Gonococcal endocarditis (disorder) | Endocarditis - gonococcal
+BMGC_DS03122,BMG_DS004285,,Multiple papillomata and wet crab yaws,,1C1D.1,Secondary yaws,A66.1,DOID:10567,late yaws,C0153234,,,,,
+BMGC_DS03123,BMG_DS004288,186973005,Latent yaws,,1C1D.3,Latent yaws,A66.8,,,C0153240,,,MONDO:0040925,latent yaws,Latent yaws | Latent yaws (disorder)
+BMGC_DS03124,BMG_DS004294,,tinea manus,,,,,DOID:13369,tinea manuum,C0153246,C000656824,,MONDO:0001699,tinea manuum,
+BMGC_DS03125,BMG_DS004295,33666009,Black piedra,,1F2D.3,Black piedra,B36.3,DOID:12711,black piedra,C0153249,,,MONDO:0005669,black piedra,Black piedra | Piedra due to Piedraia hortae | Black piedra (disorder)
+BMGC_DS03126,BMG_DS004298,70572005,Systemic candidiasis,,1F23.Y/1G40,,B37.7,,,C0153252,C536777,,MONDO:0042233,disseminated candidiasis,Disseminated candidiasis | Systemic candidiasis | Disseminated candidiasis (disorder) | Disseminated candidosis | Invasive candidiasis | Disseminated candida
+BMGC_DS03127,BMG_DS004300,63553008,Candidal endocarditis,,1F23.3Y/BB40,,B37.6,,,C0153254,,,,,Candidal endocarditis | Candidal endocarditis (disorder)
+BMGC_DS03128,BMG_DS004302,45021001,Candidal meningitis,,1F23.30,Candida meningitis,B37.5,,,C0153256,,MTHU067521,,,Candidal meningitis | Candidal meningitis (disorder)
+BMGC_DS03129,BMG_DS004303,88036000;187026005,Primary pulmonary coccidioidomycosis,,,,,,,C0153257,,,,,Primary pulmonary coccidioidomycosis | San Joaquin Valley fever | Coccidioidal pneumonitis | Coccidioidomycotic pneumonitis | Desert rheumatism | Primary pulmonary coccidioidomycosis (disorder) | Primary pulmonary coccidioidomycosis | Primary pulmonary coccidioidomycosis (disorder)
+BMGC_DS03130,BMG_DS004305,,Histoplasma capsulatum Infection,Histoplasmosis,,,,DOID:1759,American histoplasmosis,C0153261,D006660,,,,
+BMGC_DS03131,BMG_DS004309,,,,,,,DOID:11315,African histoplasmosis,C0153270,,,,,
+BMGC_DS03132,BMG_DS004314,,,,,,,DOID:12246,histoplasmosis meningitis,C0153277,,,MONDO:0001471,histoplasmosis meningitis,
+BMGC_DS03133,BMG_DS004315,187058000,Histoplasmosis with retinitis,,,,,DOID:11316,histoplasmosis retinitis,C0153278,,,MONDO:0001263,histoplasmosis retinitis,Histoplasmosis with retinitis | Histoplasmosis with retinitis (disorder)
+BMGC_DS03134,BMG_DS004316,187059008,Histoplasmosis with pericarditis,,,,,DOID:10234,histoplasmosis pericarditis,C0153279,,,MONDO:0000981,Histoplasma pericarditis,Histoplasmosis with pericarditis | Histoplasmosis with pericarditis (disorder)
+BMGC_DS03135,BMG_DS004319,20790006,Echinococcus granulosus infection of liver,,1F73.0,Echinococcus infection of liver,B67.0,,,C0153289,,,,,Echinococcus granulosus infection of liver | Echinococcus granulosus infection of liver (disorder)
+BMGC_DS03136,BMG_DS004320,75388006,Echinococcus granulosus infection of lung,,1F73.1,Echinococcus infection of lung,B67.1,,,C0153290,,,,,Echinococcus granulosus infection of lung | Echinococcus granulosus infection of lung (disorder) | Echinococcus granulosus pulmonary infection | Echinococcus granulosus lung infection
+BMGC_DS03137,BMG_DS004327,90679001,Mixed intestinal infection caused by Cestoda and/or Trematoda and/or Phylum Nemata,,,,,,,C0153303,,,,,Mixed intestinal helminthiasis | Mixed intestinal infection caused by Cestoda and/or Trematoda and/or Phylum Nemata | Mixed intestinal infection caused by Cestoda and/or Trematoda and/or Phylum Nematoda | Mixed intestinal infection caused by Cestoda and/or Trematoda and/or Phylum Nematoda (disorder)
+BMGC_DS03138,BMG_DS004341,,,,,,,DOID:8564,lip cancer,C0153340,,,MONDO:0006834,lip cancer,
+BMGC_DS03139,BMG_DS004342,,,,,,,DOID:8564,lip cancer,C0153346,,,,,
+BMGC_DS03140,BMG_DS004343,,,,,,,DOID:8564,lip cancer,C0153347,,,,,
+BMGC_DS03141,BMG_DS004344,,,,,,,DOID:8649,tongue cancer,C0153349,,,MONDO:0004631,tongue cancer,
+BMGC_DS03142,BMG_DS004345,,,,,,,DOID:8649,tongue cancer,C0153350,,,,,
+BMGC_DS03143,BMG_DS004346,,,,,,,DOID:8649,tongue cancer,C0153351,,,,,
+BMGC_DS03144,BMG_DS004347,,,,,,,DOID:8649,tongue cancer,C0153356,,,,,
+BMGC_DS03145,BMG_DS004348,,,,,,,DOID:9173,submandibular gland cancer,C0153360,,,MONDO:0004724,submandibular gland cancer,
+BMGC_DS03146,BMG_DS004349,,,,,,,DOID:8849,sublingual gland cancer,C0153361,,,MONDO:0004667,sublingual gland cancer,
+BMGC_DS03147,BMG_DS004350,,,,,,,DOID:8850,salivary gland cancer,C0153362,,,,,
+BMGC_DS03148,BMG_DS004351,,,,,,,DOID:8602,gum cancer,C0153364,,,MONDO:0005507,gingival cancer,
+BMGC_DS03149,BMG_DS004352,,,,,,,DOID:8601,upper gum cancer,C0153365,,,MONDO:0004615,upper gum cancer,
+BMGC_DS03150,BMG_DS004353,,,,,,,DOID:8618,oral cavity cancer,C0153368,,,MONDO:0021320,malignant tumor of floor of mouth,
+BMGC_DS03151,BMG_DS004354,,,,,,,DOID:8618,oral cavity cancer,C0153369,,,,,
+BMGC_DS03152,BMG_DS004355,,,,,,,DOID:8702,cheek mucosa cancer,C0153373,,,MONDO:0004645,cheek mucosa cancer,
+BMGC_DS03153,BMG_DS004356,,,,,,,DOID:9188,vestibule of mouth cancer,C0153374,,,MONDO:0004727,vestibule of mouth cancer,
+BMGC_DS03154,BMG_DS004357,,,,,,,DOID:9149,hard palate cancer,C0153375,,,MONDO:0004719,hard palate cancer,
+BMGC_DS03155,BMG_DS004358,,,,,,,DOID:8578,soft palate cancer,C0153376,,,MONDO:0004611,soft palate cancer,
+BMGC_DS03156,BMG_DS004359,,,,,,,DOID:8635,uvula cancer,C0153377,,,MONDO:0004624,uvula cancer,
+BMGC_DS03157,BMG_DS004360,,,,,,,DOID:8930,retromolar area cancer,C0153379,,,MONDO:0004682,retromolar area cancer,
+BMGC_DS03158,BMG_DS004362,,,,,,,DOID:8557,oropharynx cancer,C0153382,,,MONDO:0004608,oropharynx cancer,
+BMGC_DS03159,BMG_DS004363,,,,,,,DOID:8969,tonsillar fossa cancer,C0153384,,,MONDO:0004690,tonsillar fossa cancer,
+BMGC_DS03160,BMG_DS004364,,,,,,,DOID:8688,tonsillar pillar cancer,C0153385,,,MONDO:0004642,tonsillar pillar cancer,
+BMGC_DS03161,BMG_DS004365,,,,,,,DOID:8556,vallecula cancer,C0153386,,,MONDO:0004607,vallecula cancer,
+BMGC_DS03162,BMG_DS004366,,,,,,,DOID:8557,oropharynx cancer,C0153388,,,,,
+BMGC_DS03163,BMG_DS004367,,,,,,,DOID:8557,oropharynx cancer,C0153389,,,,,
+BMGC_DS03164,BMG_DS004368,,,,,,,DOID:8557,oropharynx cancer,C0153390,,,,,
+BMGC_DS03165,BMG_DS004369,,,,,,,DOID:9261,nasopharynx carcinoma,C0153392,,,MONDO:0021315,malignant tumor of nasopharynx,
+BMGC_DS03166,BMG_DS004370,,,,,,,DOID:9261,nasopharynx carcinoma,C0153393,,,,,
+BMGC_DS03167,BMG_DS004371,,,,,,,DOID:9261,nasopharynx carcinoma,C0153394,,,,,
+BMGC_DS03168,BMG_DS004372,,,,,,,DOID:9261,nasopharynx carcinoma,C0153395,,,,,
+BMGC_DS03169,BMG_DS004373,,,,,,,DOID:9261,nasopharynx carcinoma,C0153396,,,,,
+BMGC_DS03170,BMG_DS004374,,,,,,,DOID:8533,hypopharynx cancer,C0153398,,,MONDO:0005806,hypopharynx cancer,
+BMGC_DS03171,BMG_DS004375,,,,,,,DOID:9235,pyriform sinus cancer,C0153400,,,MONDO:0004733,pyriform sinus cancer,
+BMGC_DS03172,BMG_DS004376,,,,,,,DOID:8663,aryepiglottic fold cancer,C0153401,,,MONDO:0004637,aryepiglottic fold cancer,
+BMGC_DS03173,BMG_DS004378,,,,,,,DOID:8937,Waldeyer's ring cancer,C0153406,,,MONDO:0004685,Waldeyer's ring cancer,
+BMGC_DS03174,BMG_DS004380,,,,,,,DOID:5041,esophageal cancer,C0153413,,,,,
+BMGC_DS03175,BMG_DS004381,,,,,,,DOID:5041,esophageal cancer,C0153414,,,,,
+BMGC_DS03176,BMG_DS004382,,,,,,,DOID:5041,esophageal cancer,C0153415,,,,,
+BMGC_DS03177,BMG_DS004383,,,,,,,DOID:5041,esophageal cancer,C0153416,,,,,
+BMGC_DS03178,BMG_DS004384,,,,,,,DOID:10548,cardia cancer,C0153417,,,MONDO:0001063,cardia cancer,
+BMGC_DS03179,BMG_DS004385,,,,,,,DOID:10544,pylorus cancer,C0153418,,,MONDO:0001061,pylorus cancer,
+BMGC_DS03180,BMG_DS004386,,,,,,,DOID:10547,pyloric antrum cancer,C0153419,,,MONDO:0001062,pyloric antrum cancer,
+BMGC_DS03181,BMG_DS004387,,,,,,,DOID:10538,gastric fundus cancer,C0153420,,,,,
+BMGC_DS03182,BMG_DS004388,,,,,,,DOID:10534,stomach cancer,C0153421,,,,,
+BMGC_DS03183,BMG_DS004389,,,,,,,DOID:10534,stomach cancer,C0153422,,,,,
+BMGC_DS03184,BMG_DS004390,,,,,,,DOID:10534,stomach cancer,C0153423,,,,,
+BMGC_DS03185,BMG_DS004391,,,,,,,DOID:10154,small intestine cancer,C0153425,,,MONDO:0000956,small intestine cancer,
+BMGC_DS03186,BMG_DS004392,,,,,,,DOID:10021,duodenum cancer,C0153426,,,MONDO:0000920,duodenum cancer,
+BMGC_DS03187,BMG_DS004393,,,,,,,DOID:13499,jejunal cancer,C0153427,,,MONDO:0006815,jejunal cancer,
+BMGC_DS03188,BMG_DS004394,,,,,,,DOID:10153,ileum cancer,C0153428,,,,,
+BMGC_DS03189,BMG_DS004395,,,,,,,DOID:10152,Meckel's diverticulum cancer,C0153429,,,MONDO:0000954,Meckel diverticulum cancer,
+BMGC_DS03190,BMG_DS004396,,,,,,,DOID:260,hepatic flexure cancer,C0153433,,,MONDO:0002357,hepatic flexure cancer,
+BMGC_DS03191,BMG_DS004397,,,,,,,DOID:261,transverse colon cancer,C0153434,,,MONDO:0002361,transverse colon cancer,
+BMGC_DS03192,BMG_DS004398,,,,,,,DOID:12190,descending colon cancer,C0153435,,,MONDO:0001462,descending colon cancer,
+BMGC_DS03193,BMG_DS004399,,,,,,,DOID:12192,sigmoid colon cancer,C0153436,,,MONDO:0001464,sigmoid colon cancer,
+BMGC_DS03194,BMG_DS004400,,,,,,,DOID:1521,cecum cancer,C0153437,,,MONDO:0002033,cecum cancer,
+BMGC_DS03195,BMG_DS004401,,,,,,,DOID:218,ascending colon cancer,C0153439,,,MONDO:0002238,ascending colon cancer,
+BMGC_DS03196,BMG_DS004402,,,,,,,DOID:12191,splenic flexure cancer,C0153440,,,MONDO:0001463,splenic flexure cancer,
+BMGC_DS03197,BMG_DS004403,,,,,,,DOID:2782,rectosigmoid junction cancer,C0153443,,,MONDO:0002425,rectosigmoid junction cancer,
+BMGC_DS03198,BMG_DS004404,,,,,,,DOID:14110,anus cancer,C0153445,,,MONDO:0000405,anal canal cancer,
+BMGC_DS03199,BMG_DS004405,,,,,,,DOID:14110,anus cancer,C0153446,,,MONDO:0001879,anus cancer,
+BMGC_DS03200,BMG_DS004406,,,,,,,DOID:3121,gallbladder cancer,C0153452,,,MONDO:0005411,gallbladder cancer,
+BMGC_DS03201,BMG_DS004407,,,,,,,DOID:4606,bile duct cancer,C0153453,,,MONDO:0021321,malignant tumor of extrahepatic bile duct,
+BMGC_DS03202,BMG_DS004408,,,,,,,DOID:10020,ampulla of Vater cancer,C0153454,,,MONDO:0000919,ampulla of vater cancer,
+BMGC_DS03203,BMG_DS004409,,,,,,,DOID:1793,pancreatic cancer,C0153458,,,,,
+BMGC_DS03204,BMG_DS004410,,,,,,,DOID:1793,pancreatic cancer,C0153459,,,,,
+BMGC_DS03205,BMG_DS004411,,,,,,,DOID:1793,pancreatic cancer,C0153460,,,,,
+BMGC_DS03206,BMG_DS004412,,,,,,,DOID:3587,pancreatic ductal carcinoma,C0153461,,,,,
+BMGC_DS03207,BMG_DS004413,,,,,,,DOID:1793,pancreatic cancer,C0153463,,,,,
+BMGC_DS03208,BMG_DS004414,,,,,,,DOID:5875,retroperitoneal cancer,C0153464,,,,,
+BMGC_DS03209,BMG_DS004415,,,,,,,DOID:5875,retroperitoneal cancer,C0153465,,,MONDO:0005941,retroperitoneal cancer,
+BMGC_DS03210,BMG_DS004416,,,,,,,DOID:1725,peritoneum cancer,C0153466,,,,,
+BMGC_DS03211,BMG_DS004417,,,,,,,,,C0153467,,,MONDO:0002087,peritoneum cancer,
+BMGC_DS03212,BMG_DS004418,,,,,,,DOID:672,spleen cancer,C0153470,,,MONDO:0005966,spleen cancer,
+BMGC_DS03213,BMG_DS004420,,,,,,,DOID:1357,maxillary sinus cancer,C0153476,,,,,
+BMGC_DS03214,BMG_DS004421,,,,,,,DOID:1363,ethmoid sinus cancer,C0153477,,,MONDO:0001763,ethmoid sinus cancer,
+BMGC_DS03215,BMG_DS004422,,,,,,,DOID:1360,frontal sinus cancer,C0153478,,,MONDO:0001756,frontal sinus cancer,
+BMGC_DS03216,BMG_DS004423,,,,,,,DOID:14546,sphenoidal sinus cancer,C0153479,,,MONDO:0001994,sphenoidal sinus cancer,
+BMGC_DS03217,BMG_DS004424,,,,,,,DOID:2595,glottis cancer,C0153483,,,MONDO:0002351,glottis cancer,
+BMGC_DS03218,BMG_DS004425,,,,,,,DOID:13476,supraglottis cancer,C0153484,,,MONDO:0001724,supraglottis cancer,
+BMGC_DS03219,BMG_DS004426,,,,,,,DOID:11472,subglottis cancer,C0153485,,,MONDO:0001293,subglottis cancer,
+BMGC_DS03220,BMG_DS004427,,,,,,,DOID:13348,laryngeal cartilage cancer,C0153486,,,MONDO:0001691,laryngeal cartilage cancer,
+BMGC_DS03221,BMG_DS004428,,,,,,,DOID:11920,tracheal cancer,C0153489,,,MONDO:0001407,tracheal cancer,
+BMGC_DS03222,BMG_DS004429,,,,,,,DOID:3924,main bronchus cancer,C0153490,,,MONDO:0002811,main bronchus cancer,
+BMGC_DS03223,BMG_DS004430,,,,,,,DOID:1324,lung cancer,C0153491,,,,,
+BMGC_DS03224,BMG_DS004431,,,,,,,DOID:1324,lung cancer,C0153492,,,,,
+BMGC_DS03225,BMG_DS004432,,,,,,,DOID:1324,lung cancer,C0153493,,,,,
+BMGC_DS03226,BMG_DS004433,,,,,,,DOID:5158,pleural cancer,C0153494,,,MONDO:0006294,pleural cancer,
+BMGC_DS03227,BMG_DS004434,,,,,,,DOID:14032,malignant parietal pleura tumor,C0153495,,,MONDO:0001861,malignant parietal pleura tumor,
+BMGC_DS03228,BMG_DS004435,,,,,,,DOID:14033,malignant visceral pleura tumor,C0153496,,,MONDO:0001862,malignant visceral pleura tumor,
+BMGC_DS03229,BMG_DS004436,,,,,,,DOID:117,heart cancer,C0153500,,,MONDO:0001340,heart cancer,
+BMGC_DS03230,BMG_DS004437,,,,,,,DOID:436,posterior mediastinum cancer,C0153502,,,MONDO:0002972,posterior mediastinum cancer,
+BMGC_DS03231,BMG_DS004438,,,,,,,DOID:5559,mediastinal cancer,C0153504,,,MONDO:0005843,mediastinal cancer,
+BMGC_DS03232,BMG_DS004439,,,,,,,DOID:2338,mandibular cancer,C0153511,,,MONDO:0005837,mandibular cancer,
+BMGC_DS03233,BMG_DS004440,,,,,,,DOID:10149,long bones of lower limb cancer,C0153517,,,,,
+BMGC_DS03234,BMG_DS004441,,,,,,,DOID:10151,malignant neoplasm of short bones of lower limb,C0153518,,,MONDO:0000953,cancer of short bone of lower limb,
+BMGC_DS03235,BMG_DS004442,,,,,,,DOID:1115,sarcoma,C0153519,,,,,
+BMGC_DS03236,BMG_DS004449,,,,,,,DOID:8632,Kaposi's sarcoma,C0153560,,,,,
+BMGC_DS03237,BMG_DS004450,,,,,,,DOID:8632,Kaposi's sarcoma,C0153561,,,,,
+BMGC_DS03238,BMG_DS004451,,,,,,,DOID:8632,Kaposi's sarcoma,C0153562,,,,,
+BMGC_DS03239,BMG_DS004452,,,,,,,DOID:8632,Kaposi's sarcoma,C0153563,,,,,
+BMGC_DS03240,BMG_DS004453,,,,,,,DOID:8632,Kaposi's sarcoma,C0153564,,,,,
+BMGC_DS03241,BMG_DS004454,,,,,,,DOID:8632,Kaposi's sarcoma,C0153565,,,,,
+BMGC_DS03242,BMG_DS004455,,,,,,,DOID:363,uterine cancer,C0153567,,,MONDO:0002715,uterine cancer,
+BMGC_DS03243,BMG_DS004457,,,,,,,DOID:2021,placenta cancer,C0153572,,,MONDO:0002178,placenta cancer,
+BMGC_DS03244,BMG_DS004458,,,,,,,DOID:9460,uterine corpus cancer,C0153574,,,,,
+BMGC_DS03245,BMG_DS004459,,,,,,,DOID:9459,isthmus cancer,C0153575,,,MONDO:0004792,cancer of isthmus of fallopian tube,
+BMGC_DS03246,BMG_DS004460,,,,,,,DOID:11747,uterine adnexa cancer,C0153577,,,,,
+BMGC_DS03247,BMG_DS004461,,,,,,,DOID:1964,fallopian tube cancer,C0153579,,,MONDO:0002158,fallopian tube cancer,
+BMGC_DS03248,BMG_DS004462,,,,,,,DOID:11746,parametrium malignant neoplasm,C0153581,,,MONDO:0001350,parametrium malignant neoplasm,
+BMGC_DS03249,BMG_DS004463,,,,,,,DOID:11747,uterine adnexa cancer,C0153584,,,MONDO:0001351,uterine adnexa cancer,
+BMGC_DS03250,BMG_DS004464,,,,,,,DOID:120,female reproductive organ cancer,C0153585,,,,,
+BMGC_DS03251,BMG_DS004465,,,,,,,DOID:2401,clitoris cancer,C0153589,,,MONDO:0002290,clitoris cancer,
+BMGC_DS03252,BMG_DS004466,,,,,,,DOID:2998,testicular cancer,C0153594,,,MONDO:0005447,testicular cancer,
+BMGC_DS03253,BMG_DS004467,,,,,,,DOID:12276,malignant tumor of undescended testis,C0153595,,,MONDO:0001480,malignant tumor of undescended testis,
+BMGC_DS03254,BMG_DS004468,,,,,,,DOID:13168,prepuce cancer,C0153598,,,MONDO:0001653,prepuce cancer,
+BMGC_DS03255,BMG_DS004469,,,,,,,DOID:11839,glans penis cancer,C0153599,,,MONDO:0001388,glans penis cancer,
+BMGC_DS03256,BMG_DS004470,,,,,,,DOID:11615,penile cancer,C0153600,,,,,
+BMGC_DS03257,BMG_DS004471,,,,,,,DOID:11615,penile cancer,C0153601,,,MONDO:0001325,penile cancer,
+BMGC_DS03258,BMG_DS004472,,,,,,,DOID:10366,epididymis cancer,C0153602,,,MONDO:0001016,epididymis cancer,
+BMGC_DS03259,BMG_DS004473,,,,,,,DOID:13169,spermatic cord cancer,C0153603,,,MONDO:0001654,spermatic cord cancer,
+BMGC_DS03260,BMG_DS004474,,,,,,,DOID:518,scrotum neoplasm,C0153604,,,MONDO:0021112,scrotum cancer,
+BMGC_DS03261,BMG_DS004475,,,,,,,DOID:3856,male reproductive organ cancer,C0153606,,,MONDO:0005836,male reproductive organ cancer,
+BMGC_DS03262,BMG_DS004476,,,,,,,DOID:11814,urinary bladder anterior wall cancer,C0153611,,,MONDO:0001376,urinary bladder anterior wall cancer,
+BMGC_DS03263,BMG_DS004477,,,,,,,DOID:11811,urinary bladder posterior wall cancer,C0153612,,,MONDO:0001373,urinary bladder posterior wall cancer,
+BMGC_DS03264,BMG_DS004478,,,,,,,DOID:11809,bladder neck cancer,C0153613,,,MONDO:0001372,bladder neck cancer,
+BMGC_DS03265,BMG_DS004479,,,,,,,DOID:11818,ureteric orifice cancer,C0153614,,,MONDO:0001379,ureteric orifice cancer,
+BMGC_DS03266,BMG_DS004480,,,,,,,DOID:11817,urachus cancer,C0153615,,,MONDO:0001378,urachus cancer,
+BMGC_DS03267,BMG_DS004481,,,,,,,DOID:4919,renal pelvis carcinoma,C0153618,,,MONDO:0044919,malignant renal pelvis neoplasm,
+BMGC_DS03268,BMG_DS004482,,,,,,,DOID:11819,ureter cancer,C0153619,,191600,MONDO:0008627,ureter cancer,
+BMGC_DS03269,BMG_DS004483,,,,,,,DOID:734,urethra cancer,C0153620,,,MONDO:0004192,urethra cancer,
+BMGC_DS03270,BMG_DS004484,,,,,,,DOID:14059,paraurethral gland cancer,C0153621,,,MONDO:0001869,paraurethral gland cancer,
+BMGC_DS03271,BMG_DS004485,,,,,,,DOID:4143,orbital cancer,C0153626,,,MONDO:0002889,orbital cancer,
+BMGC_DS03272,BMG_DS004486,,,,,,,DOID:294,lacrimal gland cancer,C0153627,,,MONDO:0002464,lacrimal gland cancer,
+BMGC_DS03273,BMG_DS004487,,,,,,,DOID:5467,conjunctival cancer,C0153628,,,MONDO:0003454,conjunctival cancer,
+BMGC_DS03274,BMG_DS004488,,,,,,,DOID:6199,cornea cancer,C0153629,,,MONDO:0003802,cornea cancer,
+BMGC_DS03275,BMG_DS004489,,,,,,,DOID:12759,choroid cancer,C0153630,,,MONDO:0006700,choroid cancer,
+BMGC_DS03276,BMG_DS004490,,,,,,,DOID:12756,lacrimal duct cancer,C0153631,,,MONDO:0001580,lacrimal duct cancer,
+BMGC_DS03277,BMG_DS004491,,,,,,,DOID:2174,ocular cancer,C0153632,,,,,
+BMGC_DS03278,BMG_DS004492,,,,,,,DOID:1319,brain cancer,C0153633,,,MONDO:0001657,brain cancer,
+BMGC_DS03279,BMG_DS004493,,,,,,,DOID:12016,frontal lobe neoplasm,C0153635,,,,,
+BMGC_DS03280,BMG_DS004494,,,,,,,DOID:2135,temporal lobe neoplasm,C0153636,,,MONDO:0002218,temporal lobe cancer,
+BMGC_DS03281,BMG_DS004495,,,,,,,DOID:14384,parietal lobe neoplasm,C0153637,,,MONDO:0001952,parietal lobe cancer,
+BMGC_DS03282,BMG_DS004496,,,,,,,DOID:910,occipital lobe neoplasm,C0153638,,,,,
+BMGC_DS03283,BMG_DS004497,,,,,,,DOID:4205,cerebellum cancer,C0153640,,,MONDO:0021317,cancer of cerebellum,
+BMGC_DS03284,BMG_DS004498,,,,,,,DOID:4203,brain stem cancer,C0153641,,,MONDO:0002912,brainstem cancer,
+BMGC_DS03285,BMG_DS004499,,,,,,,DOID:368,cerebrum cancer,C0153642,,,,,
+BMGC_DS03286,BMG_DS004500,,,,,,,DOID:3093,nervous system cancer,C0153643,,,,,
+BMGC_DS03287,BMG_DS004501,,,,,,,DOID:2815,cranial nerve malignant neoplasm,C0153644,,,MONDO:0002433,malignant cranial nerve neoplasm,
+BMGC_DS03288,BMG_DS004502,,,,,,,DOID:5612,spinal cancer,C0153646,,,MONDO:0003544,spinal cord cancer,
+BMGC_DS03289,BMG_DS004503,,,,,,,DOID:7224,spinal meninges cancer,C0153647,,,MONDO:0004151,spinal meninges cancer,
+BMGC_DS03290,BMG_DS004504,,,,,,,DOID:1540,parathyroid carcinoma,C0153653,,,MONDO:0021311,malignant tumor of parathyroid gland,
+BMGC_DS03291,BMG_DS004505,,,,,,,DOID:5032,pineal gland cancer,C0153655,,,MONDO:0003249,pineal gland cancer,
+BMGC_DS03292,BMG_DS004506,,,,,,,DOID:8731,carotid body cancer,C0153656,,,MONDO:0004650,malignant carotid body paraganglioma,
+BMGC_DS03293,BMG_DS004507,,,,,,,DOID:170,endocrine gland cancer,C0153658,,,MONDO:0021069,malignant endocrine neoplasm,
+BMGC_DS03294,BMG_DS004508,,,,,,,DOID:5093,thoracic cancer,C0153661,,,MONDO:0003274,thoracic cancer,
+BMGC_DS03295,BMG_DS004510,,,,,,,DOID:12972,intrapelvic lymph node leukemic reticuloendotheliosis,C0153831,,,MONDO:0001607,intrapelvic lymph node leukemic reticuloendotheliosis,
+BMGC_DS03296,BMG_DS004511,,,,,,,DOID:709,splenic manifestation of hairy cell leukemia,C0153832,,,,,
+BMGC_DS03297,BMG_DS004512,,,,,,,DOID:13005,intra-abdominal lymph node mast cell malignancy,C0153844,,,MONDO:0001614,intra-abdominal lymph node mast cell malignancy,
+BMGC_DS03298,BMG_DS004513,,,,,,,DOID:8527,monocytic leukemia,C0153903,,,,,
+BMGC_DS03299,BMG_DS004514,,,,,,,DOID:3264,subacute leukemia,C0153924,,,MONDO:0002582,subacute leukemia,
+BMGC_DS03300,BMG_DS004530,,,,,,,DOID:10188,skin lipoma,C0153968,,,MONDO:0021630,lipoma of face,
+BMGC_DS03301,BMG_DS004531,,,,,,,DOID:10206,lipoma of spermatic cord,C0153972,,,MONDO:0000975,lipoma of spermatic cord,
+BMGC_DS03302,BMG_DS004532,,,,,,,DOID:13222,submucous uterine fibroid,C0153993,,,MONDO:0001664,submucous uterine fibroid,
+BMGC_DS03303,BMG_DS004533,,,,,,,DOID:13955,uterus interstitial leiomyoma,C0153994,,,MONDO:0001843,uterus interstitial leiomyoma,
+BMGC_DS03304,BMG_DS004534,,,,,,,DOID:13560,subserous uterine fibroid,C0153995,,,MONDO:0001745,subserous uterine fibroid,
+BMGC_DS03305,BMG_DS004535,,,,,,,DOID:0060325,cervical polyp,C0153996,,,,,
+BMGC_DS03306,BMG_DS004558,,,,,,,DOID:2517,intracranial structure hemangioma,C0154050,,,MONDO:0002328,intracranial hemangioma,
+BMGC_DS03307,BMG_DS004560,,,,,,,DOID:254,hemangioma of intra-abdominal structure,C0154052,,,MONDO:0002337,intra-abdominal hemangioma,
+BMGC_DS03308,BMG_DS004563,,,,,,,DOID:9095,esophagus carcinoma in situ,C0154059,,,MONDO:0004708,esophagus carcinoma in situ,
+BMGC_DS03309,BMG_DS004564,,,,,,,DOID:9138,stomach carcinoma in situ,C0154060,,,MONDO:0004716,stomach carcinoma in situ,
+BMGC_DS03310,BMG_DS004565,,,,,,,DOID:8826,colon carcinoma in situ,C0154061,,,MONDO:0004663,colon carcinoma in situ,
+BMGC_DS03311,BMG_DS004566,,,,,,,DOID:9174,rectum carcinoma in situ,C0154062,,,MONDO:0004725,rectum carcinoma in situ,
+BMGC_DS03312,BMG_DS004567,,,,,,,DOID:9087,anal carcinoma in situ,C0154064,,,,,
+BMGC_DS03313,BMG_DS004568,,,,,,,DOID:9024,intestine carcinoma in situ,C0154065,,,,,
+BMGC_DS03314,BMG_DS004569,,,,,,,DOID:9011,larynx carcinoma in situ,C0154069,,,MONDO:0004696,larynx carcinoma in situ,
+BMGC_DS03315,BMG_DS004570,,,,,,,DOID:8802,trachea carcinoma in situ,C0154070,,,MONDO:0004661,trachea carcinoma in situ,
+BMGC_DS03316,BMG_DS004571,,,,,,,DOID:8800,lung carcinoma in situ,C0154071,,,,,
+BMGC_DS03317,BMG_DS004572,,,,,,,DOID:8687,skin carcinoma in situ,C0154073,,,MONDO:0004641,skin carcinoma in situ,
+BMGC_DS03318,BMG_DS004573,,,,,,,DOID:8687,skin carcinoma in situ,C0154074,,,,,
+BMGC_DS03319,BMG_DS004574,,,,,,,DOID:8687,skin carcinoma in situ,C0154077,,,,,
+BMGC_DS03320,BMG_DS004575,,,,,,,DOID:8687,skin carcinoma in situ,C0154078,,,,,
+BMGC_DS03321,BMG_DS004576,,,,,,,DOID:8687,skin carcinoma in situ,C0154079,,,,,
+BMGC_DS03322,BMG_DS004577,,,,,,,DOID:8687,skin carcinoma in situ,C0154080,,,,,
+BMGC_DS03323,BMG_DS004578,,,,,,,DOID:8687,skin carcinoma in situ,C0154081,,,,,
+BMGC_DS03324,BMG_DS004579,,,,,,,DOID:8791,breast carcinoma in situ,C0154084,,,MONDO:0004658,breast carcinoma in situ,
+BMGC_DS03325,BMG_DS004580,,,,,,,DOID:9108,uterus carcinoma in situ,C0154086,,,,,
+BMGC_DS03326,BMG_DS004581,,,,,,,DOID:8634,prostate carcinoma in situ,C0154088,,,,,
+BMGC_DS03327,BMG_DS004582,,,,,,,DOID:8872,penis carcinoma in situ,C0154089,,,MONDO:0004671,penis carcinoma in situ,
+BMGC_DS03328,BMG_DS004583,,,,,,,DOID:9053,bladder carcinoma in situ,C0154091,,,MONDO:0004703,bladder carcinoma in situ,
+BMGC_DS03329,BMG_DS004584,,,,,,,DOID:9234,kidney carcinoma in situ,C0154092,,,,,
+BMGC_DS03330,BMG_DS004585,,,,,,,DOID:8792,eye carcinoma in situ,C0154094,,,MONDO:0004659,eye carcinoma in situ,
+BMGC_DS03331,BMG_DS004586,,,,,,,DOID:10719,toxic diffuse goiter,C0154138,,,,,
+BMGC_DS03332,BMG_DS004591,27059002,Postoperative hypothyroidism,,,,,DOID:1458,postsurgical hypothyroidism,C0154157,,,MONDO:0002002,postsurgical hypothyroidism,Postoperative hypothyroidism (disorder) | Postoperative hypothyroidism | Postsurgical hypothyroidism | Hypothyroidism after surgery
+BMGC_DS03333,BMG_DS004593,190279008,Iodine hypothyroidism,,,,,DOID:5083,iodine hypothyroidism,C0154159,,,MONDO:0003271,iodine hypothyroidism,Iodine hypothyroidism | Iodine hypothyroidism (disorder)
+BMGC_DS03334,BMG_DS004595,89024000;190298005,Riedel's thyroiditis,,,,,DOID:14351,Riedel's fibrosing thyroiditis,C0154162,,,MONDO:0018992,IgG4-related thyroid disease,Riedel's thyroiditis | Woody thyroiditis | Struma fibrosa thyroid | Ligneous thyroiditis | Invasive fibrous thyroiditis | Riedel's thyroiditis (disorder) | Riedel thyroiditis | Thyroiditis: [chronic fibrous] or [Riedel's] | Riedel's thyroiditis | Chronic fibrous thyroiditis | Thyroiditis: [chronic fibrous] or [Riedel's] (disorder)
+BMGC_DS03335,BMG_DS004599,190427005,Other disorders of pancreatic internal secretion,,,,E16,DOID:1428,endocrine pancreas disease,C0154189,,,,,Other disorders of pancreatic internal secretion | Other disorders of pancreatic internal secretion (disorder)
+BMGC_DS03336,BMG_DS004600,190437000,Post-surgical hypoinsulinemia,,,,,DOID:2181,post-surgical hypoinsulinemia,C0154190,,,MONDO:0002239,post-surgical hypoinsulinemia,Post-surgical hypoinsulinemia | Post-surgical hypoinsulinaemia | Post-surgical hypoinsulinemia (disorder) | Postsurgical hypoinsulinaemia | Postsurgical hypoinsulinemia | Postoperative hypoinsulinaemia | Postoperative hypoinsulinemia
+BMGC_DS03337,BMG_DS004601,11178005,Abnormality of secretion of glucagon,,,,,DOID:14427,abnormality of glucagon secretion,C0154191,,,MONDO:0001962,abnormality of glucagon secretion,Abnormality of secretion of glucagon | Abnormality of secretion of glucagon (disorder) | Abnormality of glucagon secretion
+BMGC_DS03338,BMG_DS004605,20673009,Disease of thymus gland,,,,,DOID:533,thymus gland disease,C0154199,,,MONDO:0003393,thymus gland disorder,Disorder of thymus | Disorder of thymus gland | Thymus disorder | Disorder of thymus gland (disorder)
+BMGC_DS03339,BMG_DS004608,111565003,Medulloadrenal hyperfunction,,,,,DOID:12257,medulloadrenal hyperfunction,C0154206,,,MONDO:0001473,medulloadrenal hyperfunction,Medulloadrenal hyperfunction | Medulloadrenal hyperfunction (disorder)
+BMGC_DS03340,BMG_DS004611,190533004;37295009,Hyperestrogenism,,,,,DOID:14336,estrogen excess,C0154209,,,,,Hyperoestrogenism | Oestrogen excess | Estrogen excess | Hyperestrogenism | Estrogen excess (disorder) | Hyperestrogenism | Hyperoestrogenism | Hyperestrogenism (disorder) | Oestrogen excess | Estrogen excess
+BMGC_DS03341,BMG_DS004619,111546006,Polyglandular dysfunction,,,,E31,,,C0154222,,,,,Polyglandular dysfunction | Polyglandular dysfunction (disorder)
+BMGC_DS03342,BMG_DS004632,,"Urea Cycle Disorders, Inborn","Urea Cycle Disorders, Inborn",,,,DOID:9267,urea cycle disorder,C0154246,D056806,,MONDO:0004739,urea cycle disorder,
+BMGC_DS03343,BMG_DS004633,,Lipid Metabolism Disorders,Lipid Metabolism Disorders,,,,,,C0154251,D052439,,MONDO:0002525,inherited lipid metabolism disorder,
+BMGC_DS03344,BMG_DS004634,190808009,Polyclonal hypergammaglobulinemia,,4B21,Polyclonal hypergammaglobulinaemia,D89.0,DOID:2344,polyclonal hypergammaglobulinemia,C0154254,,,MONDO:0002272,polyclonal hypergammaglobulinemia,Polyclonal hypergammaglobulinemia | Polyclonal hypergammaglobulinaemia | Polyclonal hypergammaglobulinemia (disorder)
+BMGC_DS03345,BMG_DS004640,,,,,,,DOID:2115,B cell deficiency,C0154276,,,,,
+BMGC_DS03346,BMG_DS004646,85746008,Anemia due to protein deficiency,,,,,DOID:13120,protein-deficiency anemia,C0154290,,,MONDO:0001638,protein-deficiency anemia,Anemia due to protein deficiency | Anemia related to kwashiorkor | Protein deficiency anemia | Anaemia due to protein deficiency | Anaemia related to kwashiorkor | Protein deficiency anaemia | Anemia due to protein deficiency (disorder)
+BMGC_DS03347,BMG_DS004650,74576004,Acquired thrombocytopenia,,,,,DOID:11126,acquired thrombocytopenia,C0154301,,,MONDO:0001198,acquired thrombocytopenia,Acquired thrombocytopenia | Acquired thrombocytopenia (disorder)
+BMGC_DS03348,BMG_DS004651,154836001;32035007,Chronic lymphadenitis,,,,,DOID:1602,lymphadenitis,C0154304,,,,,Chronic lymphadenitis | Chronic lymphadenitis (disorder) | Chronic lymphadenitis | Chronic adenitis | Chronic lymphadenitis (disorder)
+BMGC_DS03349,BMG_DS004654,,,,,,,DOID:1307,dementia,C0154319,,,,,
+BMGC_DS03350,BMG_DS004655,,,,,,,DOID:1203,drug-induced mental disorder,C0154325,,,,,
+BMGC_DS03351,BMG_DS004657,,,,,,,DOID:8645,subacute delirium,C0154333,,,MONDO:0004629,subacute delirium,
+BMGC_DS03352,BMG_DS004658,,,,,,,DOID:8646,substance-induced psychosis,C0154334,,,,,
+BMGC_DS03353,BMG_DS004659,,,,,,,DOID:1470,major depressive disorder,C0154409,,,,,
+BMGC_DS03354,BMG_DS004660,,,,,,,DOID:12294,atypical depressive disorder,C0154437,,,MONDO:0001485,atypical depressive disorder,
+BMGC_DS03355,BMG_DS004661,,,,,,,DOID:0060040,pervasive developmental disorder,C0154451,,,,,
+BMGC_DS03356,BMG_DS004662,,,,,,,DOID:11120,psychologic dyspareunia,C0154466,,,MONDO:0001196,psychologic dyspareunia,
+BMGC_DS03357,BMG_DS004663,,,,,,,DOID:2575,barbiturate dependence,C0154482,,,,,
+BMGC_DS03358,BMG_DS004664,,,,,,,DOID:8519,barbiturate abuse,C0154529,,,,,
+BMGC_DS03359,BMG_DS004665,,,,,,,DOID:670,amphetamine abuse,C0154536,,,,,
+BMGC_DS03360,BMG_DS004666,,,,,,,DOID:11718,antidepressant type abuse,C0154540,,,,,
+BMGC_DS03361,BMG_DS004669,,,,,,,DOID:535,sleep disorder,C0154564,,,,,
+BMGC_DS03362,BMG_DS004670,,,,,,,DOID:11507,rumination disorder,C0154575,,,MONDO:0001301,rumination disorder,
+BMGC_DS03363,BMG_DS004671,,,,,,,DOID:13365,reading disorder,C0154631,,,,,
+BMGC_DS03364,BMG_DS004672,4510004,Streptococcal meningitis,,1B53,Meningitis due to Streptococcus,G00.2,DOID:11574,streptococcal meningitis,C0154639,,,MONDO:0001316,streptococcal meningitis,Streptococcal meningitis | Streptococcal meningitis (disorder)
+BMGC_DS03365,BMG_DS004673,12166008,Staphylococcal meningitis,,1B54,Meningitis due to Staphylococcus,G00.3,,,C0154640,,,,,Staphylococcal meningitis | Staphylococcal meningitis (disorder)
+BMGC_DS03366,BMG_DS004675,192673008,Sarcoid meningitis,,,,D86.81,DOID:12055,sarcoid meningitis,C0154648,,,,,Meningitis due to sarcoidosis | Meningeal sarcoidosis | Sarcoid meningitis | Sarcoid meningitis (disorder)
+BMGC_DS03367,BMG_DS004677,25671008,Eosinophilic meningitis,,,,,DOID:10361,eosinophilic meningitis,C0154652,,,MONDO:0001015,eosinophilic meningitis,Eosinophilic meningitis | Eosinophilic meningitis (disorder)
+BMGC_DS03368,BMG_DS004678,21664006,Chronic meningitis,,8E40.Z,"Disorders of the meninges excluding infection, unspecified",G03.1,DOID:10341,chronic meningitis,C0154653,,,MONDO:0001007,chronic meningitis,Chronic meningitis | Chronic meningitis (disorder)
+BMGC_DS03369,BMG_DS004683,267687006;192804001;154996004;154995000;45864009,Senile degeneration of brain,,,,,DOID:14524,senile degeneration of brain,C0154669,,,MONDO:0001987,senile degeneration of brain,Hydrocephalus | Senile brain degen. | Senile degeneration of brain | Child cerebral degeneration | (Child cerebral degeneration) or (hydrocephalus) or (senile brain degeneration) | (Child cerebral degeneration) or (hydrocephalus) or (senile brain degeneration) (disorder) | Senile degeneration of brain | Senile degeneration of brain (disorder) | Child cerebral degeneration | Senile brain degen. | Hydrocephalus | Senile degeneration of brain | (Child cerebral degeneration) or (hydrocephalus) or (senile brain degeneration) | (Child cerebral degeneration) or (hydrocephalus) or (senile brain degeneration) (disorder) | Senile degeneration of brain | Senile degeneration of brain (disorder) | Age-related degeneration of brain
+BMGC_DS03370,BMG_DS004684,52522001,Degenerative brain disorder,,,,,DOID:1443,cerebral degeneration,C0154671,,,MONDO:0024238,cerebral degeneration,Degenerative brain disorder | Degenerative brain disorder (disorder)
+BMGC_DS03371,BMG_DS004685,55776008;267584007;192853001,Symptomatic torsion dystonia,,,,,DOID:0050835,generalized dystonia,C0154674,,,,,Symptomatic torsion dystonia | Symptomatic torsion dystonia (disorder) | (Symptomatic torsion dystonia) or (athetoid cerebral palsy) or (congenital athetosis) or (Vogt's disease) | Vogt's disease | Athetoid cerebral palsy | Symptomatic torsion dystonia | Athetosis - congenital | (Symptomatic torsion dystonia) or (athetoid cerebral palsy) or (congenital athetosis) or (Vogt's disease) (disorder)
+BMGC_DS03372,BMG_DS004686,192859002,Fragments of torsion dystonia,,,,,DOID:0050835,generalized dystonia,C0154675,,,,,Fragments of torsion dystonia | Fragments of torsion dystonia (disorder)
+BMGC_DS03373,BMG_DS004688,,Anterior Horn Cell Disease,Motor Neuron Disease,,,,DOID:4873,anterior horn cell disease,C0154681,D016472,,MONDO:0003182,anterior horn disorder,
+BMGC_DS03374,BMG_DS004689,,Lateral Sclerosis,Motor Neuron Disease,,,,DOID:230,lateral sclerosis,C0154682,D016472,,MONDO:0018155,lateral sclerosis,
+BMGC_DS03375,BMG_DS004690,29774004,Vascular myelopathy,,,,,DOID:320,vascular myelopathy,C0154685,,,MONDO:0002552,vascular myelopathy,Vascular myelopathy | Vascular myelopathy (disorder)
+BMGC_DS03376,BMG_DS004693,192914009;86489003,Idiopathic peripheral autonomic neuropathy,,8D88.Y,Other specified autonomic neuropathies,G90.0,DOID:11488,idiopathic peripheral autonomic neuropathy,C0154690,,,MONDO:0001295,idiopathic peripheral autonomic neuropathy,Idiopathic peripheral autonomic neuropathy | Idiopathic peripheral autonomic neuropathy (disorder)
+BMGC_DS03377,BMG_DS004694,,,,,,,DOID:11465,autonomic nervous system disease,C0154691,,,,,
+BMGC_DS03378,BMG_DS004696,,"Hemiplegia, Flaccid",Hemiplegia,,,,,,C0154693,D006429,,,,
+BMGC_DS03379,BMG_DS004697,,"Hemiplegia, Spastic",Hemiplegia,,,,,,C0154694,D006429,,MONDO:0001168,spastic hemiplegia,
+BMGC_DS03380,BMG_DS004698,,Diplegic Infantile Cerebral Palsy,Cerebral Palsy,,,,DOID:10965,spastic diplegia,C0154695,D002547,,,,
+BMGC_DS03381,BMG_DS004699,,"Cerebral Palsy, Quadriplegic, Infantile",Cerebral Palsy,,,,DOID:10970,spastic quadriplegic cerebral palsy,C0154697,D002547,,,,
+BMGC_DS03382,BMG_DS004700,,Monoplegic Infantile Cerebral Palsy,Cerebral Palsy,,,,DOID:10968,spastic monoplegia,C0154698,D002547,,MONDO:0001169,spastic monoplegia,
+BMGC_DS03383,BMG_DS004702,192968004;54099005,Diplegia of upper limbs,,MB51.Z,"Diplegia of upper extremities, unspecified",G83.0,DOID:862,diplegia of upper limb,C0154701,,,MONDO:0004618,diplegia of upper limb,Diplegia of upper limbs | Diplegia of upper limbs (disorder) | Diplegia of upper limbs | Paralysis of both upper limbs | Upper diplegia | Diplegia of upper limbs (disorder)
+BMGC_DS03384,BMG_DS004706,,,,,,,DOID:5129,simple partial epilepsy,C0154712,,,,,
+BMGC_DS03385,BMG_DS004707,,Migraine with Aura,Migraine with Aura,,,,DOID:10024,migraine with aura,C0154723,D020325,,MONDO:0005475,migraine with aura,
+BMGC_DS03386,BMG_DS004711,,Disorders of other cranial nerves,,,,G52,DOID:3418,glossopharyngeal nerve disease,C0154730,,,,,
+BMGC_DS03387,BMG_DS004712,,Glossopharyngeal Neuralgia,Glossopharyngeal Nerve Diseases,,,,DOID:14423,glossopharyngeal neuralgia,C0154731,D020435,,MONDO:0016372,glossopharyngeal neuralgia,
+BMGC_DS03388,BMG_DS004713,78152008,Multiple cranial nerve palsy,,,,,DOID:13866,multiple cranial nerve palsy,C0154733,,,MONDO:0001819,multiple cranial nerve palsy,Multiple cranial nerve palsy | Multiple cranial nerve palsy (disorder)
+BMGC_DS03389,BMG_DS004714,4062006,Lumbosacral plexus lesion,,,,,DOID:13913,lumbosacral plexus lesion,C0154735,,,MONDO:0001829,lumbosacral plexus lesion,Lumbosacral plexus lesion | Lumbosacral plexus lesion (disorder)
+BMGC_DS03390,BMG_DS004718,155072002;193125009,Mononeuritis of upper limb and mononeuritis multiplex,,,,,DOID:572,mononeuritis of upper limb and mononeuritis multiplex,C0154741,,,MONDO:0003607,neuritis of upper limb,Mononeuritis of upper limb and mononeuritis multiplex | Mononeuritis of upper limb and mononeuritis multiplex (disorder)
+BMGC_DS03391,BMG_DS004719,,,,,,,DOID:571,median neuropathy,C0154742,,,,,
+BMGC_DS03392,BMG_DS004720,,Ulnar Neuropathies,Ulnar Neuropathies,,,,DOID:4613,ulnar neuropathy,C0154743,D020424,,MONDO:0007006,ulnar neuropathy,
+BMGC_DS03393,BMG_DS004721,193137006;16644004,Lesion of radial nerve,,8C10.2,Lesion of radial nerve,G56.3,DOID:12170,radial nerve lesion,C0154744,,,MONDO:0006940,radial nerve lesion,Lesion of radial nerve (disorder) | Lesion of radial nerve | Radial nerve lesion | Radial neuropathy | Radial neuropathy (disorder)
+BMGC_DS03394,BMG_DS004722,,,,,,,DOID:1844,mononeuritis of upper limb,C0154746,,,,,
+BMGC_DS03395,BMG_DS004723,62235007,Mononeuritis of lower limb,,,,,DOID:9473,mononeuritis of lower limb,C0154747,,,MONDO:0004797,mononeuritis of lower limb,Mononeuritis of lower limb | Mononeuritis of lower limb (disorder)
+BMGC_DS03396,BMG_DS004724,,Lesion of Sciatic Nerve,Sciatic Neuropathy,,,,DOID:12528,lesion of sciatic nerve,C0154748,D020426,,MONDO:0001543,lesion of sciatic nerve,
+BMGC_DS03397,BMG_DS004725,365258000;359842002,Tibial nerve palsy,,,,,DOID:12529,tibial nerve palsy,C0154751,,,MONDO:0001544,tibial nerve palsy,Tibial nerve palsy | Tibial nerve palsy (disorder) | Tibial nerve palsy | Medial popliteal neuropathy | Posterior tibial neuropathy | Tibial neuropathy | Tibial neuropathy (disorder)
+BMGC_DS03398,BMG_DS004726,193148004,Plantar nerve lesion,,,,,DOID:12524,plantar nerve lesion,C0154752,,,MONDO:0001541,plantar nerve lesion,Plantar nerve lesion | Plantar nerve lesion (disorder)
+BMGC_DS03399,BMG_DS004728,193164007;33209009,Idiopathic progressive polyneuropathy,,,,,DOID:10593,idiopathic progressive polyneuropathy,C0154756,,,MONDO:0001073,idiopathic progressive polyneuropathy,Idiopathic progressive polyneuropathy | Idiopathic progressive polyneuropathy (disorder)
+BMGC_DS03400,BMG_DS004729,,,,,,,DOID:2537,inflammatory and toxic neuropathy,C0154758,,,,,
+BMGC_DS03401,BMG_DS004730,193177003,Polyneuropathy in collagen vascular disease,,,,,DOID:13649,polyneuropathy in collagen vascular disease,C0154759,,,MONDO:0001765,polyneuropathy in collagen vascular disease,Polyneuropathy in collagen vascular disease | Neuropathy in vasculitis and connective tissue disease | Polyneuropathy in collagen vascular disease (disorder)
+BMGC_DS03402,BMG_DS004731,7339009,Polyneuropathy caused by drug,,,,,DOID:14184,polyneuropathy due to drug,C0154762,,,MONDO:0001904,polyneuropathy due to drug,Drug-related polyneuropathy | Polyneuropathy caused by drug (disorder) | Polyneuropathy caused by drug
+BMGC_DS03403,BMG_DS004735,193268004;1493002,Acute endophthalmitis,,,,,DOID:11752,acute endophthalmitis,C0154773,,,MONDO:0017202,acute endophthalmitis,Acute endophthalmitis | Acute endophthalmitis (disorder)
+BMGC_DS03404,BMG_DS004736,13978000;193269007,Chronic endophthalmitis,,,,,DOID:10697,chronic endophthalmitis,C0154774,,,MONDO:0017203,chronic endophthalmitis,Chronic endophthalmitis | Chronic endophthalmitis (disorder)
+BMGC_DS03405,BMG_DS004737,12371008,Ophthalmia nodosa,,,,H16.24,DOID:9722,ophthalmia nodosa,C0154775,,,MONDO:0004861,ophthalmia nodosa,Ophthalmia nodosa | Caterpillar-hair ophthalmia | Caterpillar ophthalmia | Ophthalmia nodosa (disorder)
+BMGC_DS03406,BMG_DS004738,62585004,Degenerative disorder of eye,,,,,DOID:9799,eye degenerative disease,C0154777,,,MONDO:0004884,eye degenerative disorder,Degenerative disorder of globe | Degenerative disorder of eye | Degenerative disorder of eye (disorder)
+BMGC_DS03407,BMG_DS004739,,"Myopia, Degenerative","Myopia, Degenerative",,,,DOID:11829,degenerative myopia,C0154778,D047728,,MONDO:0001383,degenerative myopia,
+BMGC_DS03408,BMG_DS004740,,Other degenerative disorders of globe,,,,H44.39,DOID:1242,globe disease,C0154780,,,,,
+BMGC_DS03409,BMG_DS004741,2251002,Primary hypotony of eye,,,,H44.44,DOID:12349,primary eye hypotony,C0154782,,,MONDO:0001503,primary eye hypotony,Primary hypotony of eye | Primary hypotony of eye (disorder)
+BMGC_DS03410,BMG_DS004742,23360000;193291000;4229009,Blind hypotensive eye,,,,,DOID:11766,blind hypotensive eye,C0154788,,,MONDO:0001360,blind hypotensive eye,Blind hypotensive eye | Blind hypotensive eye (disorder) | Atrophy of globe | Globe of eye shrunken | Atrophia bulbi | Shrunken eyeball | Phthysis bulbi | Eyeball atrophic | Phthisis bulbi | Phthysical eye | Globe of eye shrunken (disorder) | Phthisical eye
+BMGC_DS03411,BMG_DS004743,193286001;264008,Blind hypertensive eye,,,,,DOID:11776,absolute glaucoma,C0154789,,,MONDO:0001363,blind hypertensive eye,(Blind hypertensive eye) or (glaucoma absolute) | Blind hypertensive eye | Glaucoma - absolute | Absolute glaucoma | (Blind hypertensive eye) or (glaucoma absolute) (disorder) | Blind hypertensive eye | Blind hypertensive eye (disorder)
+BMGC_DS03412,BMG_DS004745,20842008,Luxation of eye,,,,,DOID:1241,luxation of globe,C0154806,,,MONDO:0001523,luxation of globe,Luxation of globe | Luxation of eye | Luxation of eye (disorder)
+BMGC_DS03413,BMG_DS004748,193332006;83405000,Flat retinoschisis,,,,,DOID:8464,flat retinoschisis,C0154817,,,MONDO:0004578,flat retinoschisis,Flat retinoschisis | Flat retinoschisis (disorder)
+BMGC_DS03414,BMG_DS004756,59276001;154679002,Proliferative diabetic retinopathy,,,,,DOID:13207,proliferative diabetic retinopathy,C0154830,,,MONDO:0001660,proliferative diabetic retinopathy,Proliferative diabetic retinopathy | Proliferative retinopathy with diabetes mellitus | PDR - proliferative diabetic retinopathy | Proliferative retinopathy due to diabetes mellitus (disorder) | Proliferative retinopathy due to diabetes mellitus | Proliferative diabetic retinopathy | Proliferative diabetic retinopathy (disorder)
+BMGC_DS03415,BMG_DS004757,193359003;25506007,Exudative retinopathy,,,,H35.02,DOID:7765,Coats disease,C0154832,,300216;MTHU009658,MONDO:0010269,Coats disease,Exudative retinopathy | Exudative retinopathy (disorder)
+BMGC_DS03416,BMG_DS004758,,,,,,,DOID:2462,retinal vascular disease,C0154833,,,MONDO:0002311,retinal vascular disorder,
+BMGC_DS03417,BMG_DS004759,,,,,,,DOID:11295,retinal microaneurysm,C0154834,,,MONDO:0001257,retinal microaneurysm,
+BMGC_DS03418,BMG_DS004760,84884003,Retinal telangiectasia,,,,,DOID:7736,retinal telangiectasia,C0154835,,MTHU039199,MONDO:0004348,retinal telangiectasia,Retinal telangiectasia | Retinal telangiectasia (disorder) | Retinal grouped capillary aneurysms
+BMGC_DS03419,BMG_DS004763,776009,Partial retinal artery occlusion,,,,H34.21,DOID:14522,partial arterial retinal occlusion,C0154839,,,MONDO:0001985,partial arterial retinal occlusion,Partial arterial retinal occlusion | Partial retinal artery occlusion | Partial occlusion of retinal artery | Partial occlusion of retinal artery (disorder)
+BMGC_DS03420,BMG_DS004764,87224000,Transient arterial retinal occlusion,,,,,DOID:8482,transient retinal arterial occlusion,C0154840,,,MONDO:0004583,transient retinal arterial occlusion,Transient arterial retinal occlusion | Transient arterial retinal occlusion (disorder)
+BMGC_DS03421,BMG_DS004765,193378003;68478007,Central retinal vein occlusion,,,,H34.81,DOID:2450,central retinal vein occlusion,C0154841,,,MONDO:0002303,central retinal vein occlusion,(Central retinal vein occlusion) or (retinal vein thrombosis) | Central retinal vein occlusion | Retinal vein thrombosis | (Central retinal vein occlusion) or (retinal vein thrombosis) (disorder) | Central retinal vein occlusion | CRVT - Central retinal vein thrombosis | CRVO - Central retinal vein occlusion | Central retinal vein thrombosis | Central retinal vein occlusion (disorder)
+BMGC_DS03422,BMG_DS004766,,,,,,,DOID:13514,venous tributary occlusion of retina,C0154842,,,,,
+BMGC_DS03423,BMG_DS004768,14046000,Cystoid macular retinal degeneration,,,,,DOID:14245,cystoid macular retinal degeneration,C0154850,,,MONDO:0001919,cystoid macular retinal degeneration,Cystoid macular retinal degeneration | Cystoid macular retinal degeneration (disorder)
+BMGC_DS03424,BMG_DS004769,69134001,Paving stone retinal degeneration,,,,,DOID:12166,cobblestone retinal degeneration,C0154854,,,MONDO:0001456,cobblestone retinal degeneration,Paving stone retinal degeneration | Paving stone retinal degeneration (disorder) | Cobblestone retinal degeneration | Pavingstone retinal degeneration | Paving-stone retinal degeneration | Cobblestone degeneration | Pavingstone degeneration
+BMGC_DS03425,BMG_DS004770,37075008,Microcystoid retinal degeneration,,,,,DOID:12164,Blessig's cysts,C0154855,,,MONDO:0001454,Blessig's cysts,Iwanoff's cysts | Blessig's cysts | Peripheral cystoid retinal degeneration | Peripheral cystoid degeneration of retina of eye | Peripheral cystoid degeneration of retina of eye (disorder)
+BMGC_DS03426,BMG_DS004771,3577000,Retinal lattice degeneration,,,,,DOID:12165,retinal lattice degeneration,C0154856,,,MONDO:0001455,retinal lattice degeneration,Retinal lattice degeneration | Palisade degeneration of retina | Retinal lattice degeneration (disorder) | Lattice retinal degeneration | LD - Lattice degeneration | Lattice degeneration
+BMGC_DS03427,BMG_DS004772,54184008,Senile reticular retinal degeneration,,,,,DOID:12163,senile reticular retinal degeneration,C0154857,,,MONDO:0001453,senile reticular retinal degeneration,Senile reticular retinal degeneration | Senile reticular retinal degeneration (disorder) | Senile reticular degeneration
+BMGC_DS03428,BMG_DS004773,35545005,Secondary pigmentary retinal degeneration,,,,,DOID:12162,pseudoretinitis pigmentosa,C0154858,,,,,Secondary pigmentary retinal degeneration | Pseudoretinitis pigmentosa | Secondary pigmentary retinal degeneration (disorder)
+BMGC_DS03429,BMG_DS004774,193397003;60676002,Secondary vitreoretinal degeneration,,,,H35.46,DOID:12167,secondary vitreoretinal degeneration,C0154859,,,MONDO:0001457,secondary vitreoretinal degeneration,Secondary vitreoretinal degeneration | Secondary vitreoretinal degeneration (disorder)
+BMGC_DS03430,BMG_DS004775,41799005,Hereditary retinal dystrophy,,9B70,Inherited retinal dystrophies,H35.5,DOID:0110838;DOID:0110362;DOID:0110385;DOID:0110217;DOID:0110400;DOID:0110367;DOID:0080350;DOID:0110189;DOID:0110215;DOID:0110360;DOID:0110078;DOID:8500;DOID:0110842;DOID:0050572;DOID:0110352;DOID:0110371;DOID:0110411;DOID:0110079;DOID:0110412;DOID:0110419;DOID:0110363;DOID:0110393;DOID:0110831;DOID:0110830;DOID:0110840;DOID:0110373;DOID:0110369;DOID:0110841;DOID:0060863;DOID:0110392;DOID:0110395;DOID:0110421;DOID:0110389;DOID:0110839;DOID:0110407;DOID:0110374;DOID:0110401;DOID:0110416;DOID:0110826;DOID:0110402;DOID:0110333;DOID:0110410;DOID:0110418;DOID:0110370;DOID:0110359;DOID:0110375;DOID:0110394;DOID:0110016;DOID:0110396;DOID:0110379;DOID:0110377;DOID:0110422;DOID:0110382;DOID:0110836;DOID:0110420;DOID:0110398;DOID:0110365;DOID:0110361;DOID:0110364;DOID:0110832;DOID:0110833;DOID:0110834;DOID:0110837;DOID:0110380;DOID:0110118;DOID:0110835;DOID:0110005,retinitis pigmentosa 47 | retinitis pigmentosa 22 | retinitis pigmentosa 43 | retinitis pigmentosa 44 | retinitis pigmentosa 50 | retinitis pigmentosa 67 | retinitis pigmentosa with or without situs inversus | Usher syndrome type 1G | Usher syndrome type 3A | Usher syndrome type 2A | retinitis pigmentosa 58 | retinitis pigmentosa 48 | retinitis pigmentosa 49 | Leber congenital amaurosis 8 | retinitis pigmentosa 69 | retinitis pigmentosa 77 | retinitis pigmentosa 39 | retinitis pigmentosa 45 | Usher syndrome type 2D | retinitis pigmentosa 23 | Usher syndrome type 1D | retinitis pigmentosa 61 | retinitis pigmentosa 40 | patterned macular dystrophy | Leber congenital amaurosis 2 | retinitis pigmentosa 63 | retinitis pigmentosa 70 | Leber congenital amaurosis 5 | retinitis pigmentosa 56 | retinitis pigmentosa 55 | retinitis pigmentosa 73 | retinitis pigmentosa 28 | Usher syndrome type 1 | Leber congenital amaurosis 9 | Leber congenital amaurosis 1 | Leber congenital amaurosis 7 | retinitis pigmentosa 59 | Leber congenital amaurosis 15 | retinitis pigmentosa 68 | retinitis pigmentosa 62 | retinitis pigmentosa Y-linked | retinitis pigmentosa 51 | Usher syndrome type 3B | retinitis pigmentosa 72 | dominant pericentral pigmentary retinopathy | Usher syndrome type 1C | Usher syndrome type 1J | Usher syndrome type 2C | late-adult onset retinitis pigmentosa | retinitis pigmentosa 38 | retinitis pigmentosa 60 | autosomal recessive pericentral pigmentary retinopathy | retinitis pigmentosa 66 | retinitis pigmentosa 71 | Leber congenital amaurosis 17 | retinitis pigmentosa 57 | Usher syndrome type 1F | Usher syndrome type 1E | retinitis pigmentosa 24 | cone-rod dystrophy | hereditary retinal dystrophy | Leber congenital amaurosis 16 | retinitis pigmentosa 75 | Usher syndrome type 1H | Usher syndrome type 1K | retinitis pigmentosa 54 | retinitis pigmentosa 74,C0154860,,,,,Hereditary retinal dystrophy | Hereditary retinal dystrophy (disorder)
+BMGC_DS03431,BMG_DS004776,,,,,,,DOID:14253,retinal dystrophy in systemic or cerebroretinal lipidoses,C0154861,,,MONDO:0001925,retinal dystrophy in systemic or cerebroretinal lipidoses,
+BMGC_DS03432,BMG_DS004777,79556007,Vitreoretinal dystrophy,,,,H35.51,DOID:14251,vitreoretinal dystrophy,C0154863,,,MONDO:0001923,vitreoretinal dystrophy,Vitreoretinal dystrophy | Vitreoretinal dystrophy (disorder)
+BMGC_DS03433,BMG_DS004779,,Dystrophies primarily involving the retinal pigment epithelium,,,,H35.54,DOID:14252,dystrophies primarily involving the retinal pigment epithelium,C0154865,,,MONDO:0001924,dystrophies primarily involving the retinal pigment epithelium,
+BMGC_DS03434,BMG_DS004780,,,,,,,DOID:13227,retinal dystrophies primarily involving Bruch's membrane,C0154866,,,MONDO:0001666,retinal dystrophies primarily involving Bruch's membrane,
+BMGC_DS03435,BMG_DS004781,15847003,Focal chorioretinitis,,9B65.2,Chorioretinal inflammation,H30.0,DOID:1979,focal chorioretinitis,C0154870,,,MONDO:0002164,focal chorioretinitis,Focal chorioretinitis | Focal retinochoroiditis | Focal chorioretinitis (disorder)
+BMGC_DS03436,BMG_DS004784,410471004,Neuroretinitis,Retinitis,,,,DOID:10176,neuroretinitis,C0154874,D012173,,MONDO:0000958,neuroretinitis,Neuroretinitis (disorder) | Neuroretinitis | Papilloretinitis
+BMGC_DS03437,BMG_DS004787,78769001,Disseminated chorioretinitis,,9B65.2,Chorioretinal inflammation,H30.1,DOID:8787,disseminated chorioretinitis,C0154879,,,MONDO:0004657,disseminated chorioretinitis,Disseminated chorioretinitis | Disseminated retinochoroiditis | Disseminated chorioretinitis (disorder)
+BMGC_DS03438,BMG_DS004793,,,,,,,DOID:11283,peripheral scars of retina,C0154888,,,,,
+BMGC_DS03439,BMG_DS004794,38513001,Senile atrophy of choroid,,,,,DOID:9776,Senile atrophy of choroid,C0154891,,,MONDO:0004879,senile atrophy of choroid,Senile atrophy of choroid | Senile atrophy of choroid (disorder)
+BMGC_DS03440,BMG_DS004795,193463006,Diffuse secondary choroid atrophy,,,,,DOID:981,diffuse secondary choroid atrophy,C0154892,,,MONDO:0004886,diffuse secondary choroid atrophy,Diffuse secondary choroid atrophy | Diffuse secondary choroid atrophy (disorder)
+BMGC_DS03441,BMG_DS004796,74469006,Hereditary choroidal dystrophy,,9B61,Choroidal dystrophy,H31.2,DOID:9794,hereditary choroidal atrophy,C0154893,,,MONDO:0004883,hereditary choroidal atrophy,Hereditary choroidal dystrophy | Hereditary choroidal atrophy | Hereditary choroidal dystrophy (disorder)
+BMGC_DS03442,BMG_DS004797,193466003,Partial circumpapillary choroid dystrophy,,,,,DOID:9811,partial circumpapillary choroid dystrophy,C0154895,,,MONDO:0004888,partial circumpapillary choroid dystrophy,Partial circumpapillary choroid dystrophy | Partial circumpapillary dystrophy of choroid | Partial peripapillary dystrophy of choroid (disorder) | Partial peripapillary dystrophy of choroid | Partial peripapillary choroidal dystrophy
+BMGC_DS03443,BMG_DS004798,59753003,Total circumpapillary dystrophy of choroid,,,,,DOID:9842,total circumpapillary dystrophy of choroid,C0154896,,,MONDO:0004898,total circumpapillary dystrophy of choroid,Total circumpapillary dystrophy of choroid | Total peripapillary choroidal dystrophy | Total peripapillary dystrophy of choroid (disorder) | Total peripapillary dystrophy of choroid
+BMGC_DS03444,BMG_DS004799,,,,,,,DOID:9820,central gyrate choroidal dystrophy,C0154898,,,MONDO:0004889,total central choroidal atrophy,
+BMGC_DS03445,BMG_DS004805,17657000,Disorder of iris and ciliary body,,,,,,,C0154907,,,,,Cyclitis | Cyclitis (disorder)
+BMGC_DS03446,BMG_DS004807,12630008;193485000,Primary iridocyclitis,,,,H20.01,DOID:9383,iridocyclitis,C0154909,,,,,Primary iridocyclitis | Primary iridocyclitis (disorder)
+BMGC_DS03447,BMG_DS004809,193487008,Secondary infected iridocyclitis,,,,,DOID:9389,infectious anterior uveitis,C0154911,,,MONDO:0017210,infectious anterior uveitis,Secondary infected iridocyclitis | Secondary infected iridocyclitis (disorder)
+BMGC_DS03448,BMG_DS004812,51995000,Rubeosis iridis,,9A8Z,"Disorders of the anterior chamber, unspecified",H21.1,DOID:14000,rubeosis iridis,C0154916,,,MONDO:0001855,rubeosis iridis,Rubeosis iridis | Rubeosis iridis (disorder) | Iris neovascularisation | Iris neovascularization | New vessels in iris | NVI - New vessels iris | Rubeotic iris
+BMGC_DS03449,BMG_DS004824,,,,,,,DOID:13327,anatomical narrow angle borderline glaucoma,C0154941,,,MONDO:0001686,anatomical narrow angle borderline glaucoma,
+BMGC_DS03450,BMG_DS004825,66990007,Residual stage of open angle glaucoma,,,,,DOID:1066,residual stage of open angle glaucoma,C0154944,,,MONDO:0001094,residual stage of open angle glaucoma,Residual stage of open angle glaucoma | Residual stage of open angle glaucoma (disorder)
+BMGC_DS03451,BMG_DS004826,65460003,Intermittent angle-closure glaucoma,,,,H40.23,DOID:13549,interval angle-closure glaucoma,C0154945,,,MONDO:0001742,interval angle-closure glaucoma,Intermittent angle-closure glaucoma | Interval angle-closure glaucoma | Subacute angle-closure glaucoma | Intermittent angle-closure glaucoma (disorder) | Subacute closed-angle glaucoma | Intermittent closed-angle glaucoma | Prodromal angle closure glaucoma
+BMGC_DS03452,BMG_DS004827,30041005,Acute angle-closure glaucoma,,,,H40.21,DOID:13862,acute closed-angle glaucoma,C0154946,,,MONDO:0001817,acute closed-angle glaucoma,Acute angle-closure glaucoma | Acute angle-closure glaucoma (disorder) | AACG - Acute angle closure glaucoma
+BMGC_DS03453,BMG_DS004828,33647009,Anatomical narrow angle glaucoma,,,,,DOID:14445,chronic closed-angle glaucoma,C0154947,,,MONDO:0001966,chronic closed-angle glaucoma,Anatomical narrow angle glaucoma | Narrow cleft glaucoma | Chronic angle-closure glaucoma | Chronic closed-angle glaucoma | Chronic narrow angle glaucoma | Anatomical narrow angle glaucoma (disorder) | CNAG - Chronic narrow angle glaucoma
+BMGC_DS03454,BMG_DS004829,,Residual stage of angle-closure glaucoma,,,,H40.24,DOID:1404,residual stage angle-closure glaucoma,C0154948,,,MONDO:0001864,residual stage angle-closure glaucoma,
+BMGC_DS03455,BMG_DS004834,,,,,,,DOID:12571,phacogenic glaucoma,C0154959,,,,,
+BMGC_DS03456,BMG_DS004839,29369005,Hypersecretion glaucoma,,,,H40.82,DOID:11148,hypersecretion glaucoma,C0154968,,,MONDO:0001205,hypersecretion glaucoma,Hypersecretion glaucoma | Hypersecretion glaucoma (disorder)
+BMGC_DS03457,BMG_DS004843,193588001;78875003,Cortical senile cataract,,,,,DOID:13574,cortical senile cataract,C0154980,,,MONDO:0001749,cortical senile cataract,Cortical senile cataract | Cortical senile cataract (disorder)
+BMGC_DS03458,BMG_DS004847,81519008,Transient refractive change,,,,,DOID:11850,transient refractive change,C0155000,,,MONDO:0001390,transient refractive change,Transient refractive change | Transient refractive change (disorder)
+BMGC_DS03459,BMG_DS004851,79195003,Abnormal retinal correspondence,,,,H53.31,DOID:12668,abnormal retinal correspondence,C0155010,,,MONDO:0001565,abnormal retinal correspondence,Abnormal retinal correspondence | Abnormal retinal correspondence (disorder) | ARC - Abnormal retinal correspondence | Anomalous retinal correspondence
+BMGC_DS03460,BMG_DS004852,,"Color Blindness, Red",Color Vision Defects,,,,DOID:13910,red color blindness,C0155015,D003117,303900,MONDO:0010565,red color blindness,
+BMGC_DS03461,BMG_DS004853,,"Color Blindness, Red-Green",Color Vision Defects,,,,DOID:13909,red-green color blindness,C0155016,D003117,303800,MONDO:0010564,red-green color blindness,
+BMGC_DS03462,BMG_DS004854,,"Color Blindness, Blue",Color Vision Defects,,,,DOID:11661,blue color blindness,C0155017,D003117,190900,MONDO:0008610,blue color blindness,
+BMGC_DS03463,BMG_DS004855,,"Color Blindness, Acquired",Color Vision Defects,,,,DOID:13912,acquired color blindness,C0155018,D003117,,MONDO:0001828,acquired color blindness,
+BMGC_DS03464,BMG_DS004856,50455002,Abnormal dark adaptation curve,,,,H53.61,DOID:11874,abnormal threshold of rods,C0155019,,,MONDO:0001396,abnormal threshold of rods,Abnormal dark adaptation curve | Abnormal threshold of rods | Abnormal threshold of cones | Delayed adaptation of cones | Delayed adaptation of rods | Abnormal dark adaptation curve (disorder) | Dark adaptation abnormality
+BMGC_DS03465,BMG_DS004857,,,,,,,DOID:1432,blindness,C0155020,,,,,
+BMGC_DS03466,BMG_DS004858,47398006,Marginal corneal ulcer,,,,H16.04,DOID:10441,marginal corneal ulcer,C0155067,,,MONDO:0001034,marginal corneal ulcer,Marginal corneal ulcer | Marginal corneal ulcer (disorder)
+BMGC_DS03467,BMG_DS004859,193760005;111520007,Ring corneal ulcer,,,,H16.02,DOID:10444,ring corneal ulcer,C0155068,,,MONDO:0001037,ring corneal ulcer,Ring corneal ulcer | Ring corneal ulcer (disorder)
+BMGC_DS03468,BMG_DS004860,193761009;7426009,Central corneal ulcer,,,,H16.01,DOID:9910,central corneal ulcer,C0155069,,,MONDO:0004918,central corneal ulcer,Central corneal ulcer | Central corneal ulcer (disorder)
+BMGC_DS03469,BMG_DS004861,6395007;193762002;267633000,Hypopyon ulcer,,,,,DOID:10442,hypopyon ulcer,C0155070,,,MONDO:0001035,hypopyon ulcer,Hypopyon ulcer | Hypopyon ulcer (disorder) | Corneal ulcer with hypopyon | Ulcer: [hypopyon] or [serpiginous] | Hypopyon ulcer | Serpiginous ulcer | Ulcer: [hypopyon] or [serpiginous] (disorder) | Hypopyon ulcer | Hypopyon ulcer (disorder)
+BMGC_DS03470,BMG_DS004862,397977001;59939007,Mycotic corneal ulcer,,,,H16.06,DOID:10440,mycotic corneal ulcer,C0155071,,,MONDO:0001033,mycotic corneal ulcer,Mycotic corneal ulcer (disorder) | Mycotic corneal ulcer | Mycotic corneal ulcer | Fungal infection of cornea | Keratomycosis | Mycotic keratitis | Fungal corneal ulcer | Mycotic corneal ulcer (disorder)
+BMGC_DS03471,BMG_DS004863,22440001,Mooren's ulcer,,,,,DOID:10439,Mooren's ulcer,C0155072,,,MONDO:0001032,Mooren ulcer,Mooren's ulcer | Mooren's ulcer (disorder) | Mooren ulcer | Mooren's corneal ulcer
+BMGC_DS03472,BMG_DS004864,27019000,Superficial keratitis,,,,,DOID:12196,superficial keratitis,C0155074,,,MONDO:0001465,superficial keratitis,Superficial keratitis | Superficial keratitis (disorder)
+BMGC_DS03473,BMG_DS004865,2853006,Macular keratitis,,,,H16.11,DOID:11871,macular keratitis,C0155076,,,MONDO:0001395,macular keratitis,Macular keratitis | Macular keratitis (disorder)
+BMGC_DS03474,BMG_DS004866,51286002,Filamentary keratitis,,,,H16.12,DOID:4664,filamentary keratitis,C0155077,,MTHU053349,MONDO:0003082,filamentary keratitis,Filamentary keratitis | Filamentary keratitis (disorder) | Filamentary keratopathy
+BMGC_DS03475,BMG_DS004867,1714005,Photokeratitis,,,,H16.13,DOID:13626,photokeratitis,C0155078,,,MONDO:0001760,photokeratitis,Photokeratitis | Photokeratitis (disorder)
+BMGC_DS03476,BMG_DS004868,193773009;67895005,Phlyctenular keratoconjunctivitis,,,,H16.25,DOID:11581,phlyctenulosis,C0155080,,,MONDO:0001317,phlyctenulosis,Phlyctenular keratoconjunctivitis | Phlyctenular keratoconjunctivitis (disorder) | Phlyctenular keratoconjunctivitis | Phlyctenulosis | Strumous ophthalmia | Phlyctenular ophthalmia | Phlyctenular keratitis | Phlyctenular keratoconjunctivitis (disorder)
+BMGC_DS03477,BMG_DS004870,193777005;77080005,Neurotrophic keratoconjunctivitis,,,,H16.23,DOID:12125,neurotrophic keratoconjunctivitis,C0155084,,,MONDO:0001440,neurotrophic keratoconjunctivitis,Neurotrophic keratoconjunctivitis | Neurotrophic keratoconjunctivitis (disorder)
+BMGC_DS03478,BMG_DS004871,193783008,Interstitial and deep keratitis,,9A78.Z,"Certain specified disorders of cornea, unspecified",H16.3,DOID:9858,deep keratitis,C0155087,,,,,Interstitial and deep keratitis | Interstitial and deep keratitis (disorder)
+BMGC_DS03479,BMG_DS004872,1763009,Interstitial keratitis,,,,,DOID:9857,interstitial keratitis,C0155088,,,MONDO:0004902,interstitial keratitis,Interstitial keratitis | Interstitial keratitis (disorder) | Stromal keratitis | IK - Interstitial keratitis
+BMGC_DS03480,BMG_DS004873,193785001;267635007;17157001,Diffuse interstitial keratitis,,,,H16.32,DOID:13353,diffuse interstitial keratitis,C0155089,,,MONDO:0001694,diffuse interstitial keratitis,Diffuse interstitial keratitis (& [Cogan's syndrome]) | Diffuse interstitial keratitis | Cogan's syndrome | Diffuse interstitial keratitis (& [Cogan's syndrome]) (disorder) | Diffuse interstitial keratitis | Diffuse interstitial keratitis (disorder)
+BMGC_DS03481,BMG_DS004874,27886001,Sclerosing keratitis,,,,H16.33,DOID:14444,sclerosing keratitis,C0155090,,,MONDO:0001965,sclerosing keratitis,Sclerosing keratitis | Sclerosing keratitis (disorder)
+BMGC_DS03482,BMG_DS004875,64366002,Corneal abscess,,,,H16.31,DOID:11543,corneal abscess,C0155091,,,MONDO:0001307,corneal abscess,Corneal abscess | Corneal abscess (disorder)
+BMGC_DS03483,BMG_DS004879,2102007,Deep vascularization of cornea,,,,H16.44,DOID:12087,deep corneal vascularisation,C0155095,,,MONDO:0001430,deep corneal vascularisation,Deep vascularization of cornea | Deep vascularisation of cornea | Deep vascularization of cornea (disorder) | Deep corneal vascularisation | Deep corneal vascularization
+BMGC_DS03484,BMG_DS004881,28143002;193801004,Phthisical cornea,,,,,DOID:11793,phthisical cornea,C0155102,,,MONDO:0001368,phthisical cornea,Phthisical cornea | Phthisical cornea (disorder) | Phthisical cornea | Phthisical cornea (finding)
+BMGC_DS03485,BMG_DS004882,18377001,Anterior corneal pigmentation,,,,,DOID:12307,anterior corneal pigmentation,C0155104,,,MONDO:0001488,anterior corneal pigmentation,Anterior corneal pigmentation | Anterior corneal pigmentation (disorder)
+BMGC_DS03486,BMG_DS004883,55031000,Stromal corneal pigmentation,,,,,DOID:12311,stromal corneal pigmentation,C0155105,,,MONDO:0006613,stromal corneal pigmentation,Stromal corneal pigmentation | Stromal corneal pigmentation (disorder)
+BMGC_DS03487,BMG_DS004884,11293004;193807000;267639001,Posterior corneal pigmentation,,,,,DOID:13448,posterior corneal pigmentation,C0155106,,,MONDO:0001717,posterior corneal pigmentation,Posterior corneal pigmentation | Posterior corneal pigmentation (disorder) | Posterior corneal pigmentation (& [Krukenberg spindle]) | Posterior corneal pigmentation | Krukenberg spindle | Posterior corneal pigmentation (& [Krukenberg spindle]) (disorder)
+BMGC_DS03488,BMG_DS004885,21328003,Argentous corneal deposit,,,,,DOID:13447,corneal argyrosis,C0155108,,,MONDO:0001716,corneal argyrosis,Argentous corneal deposit | Argentous corneal deposit (disorder) | Argyrosis of cornea
+BMGC_DS03489,BMG_DS004886,193813009;1794009,Idiopathic corneal edema,,,,H18.22,DOID:11033,idiopathic corneal edema,C0155109,,,MONDO:0001182,idiopathic corneal edema,Idiopathic corneal edema | Idiopathic corneal oedema | Idiopathic corneal edema (disorder)
+BMGC_DS03490,BMG_DS004887,27536004;193814003,Secondary corneal edema,,,,H18.23,DOID:11032,secondary corneal edema,C0155110,,,MONDO:0001181,secondary corneal edema,Secondary corneal edema | Secondary corneal oedema | Secondary corneal edema (disorder) | Secondary corneal oedema | Secondary corneal edema | Secondary corneal edema (disorder)
+BMGC_DS03491,BMG_DS004888,193815002;57207003,Bullous keratopathy,,9A78.20,Bullous keratopathy,H18.1,DOID:11031,bullous keratopathy,C0155111,,,MONDO:0001180,bullous keratopathy,Bullous keratopathy | Bullous keratopathy (disorder) | Bullous keratopathy | BK - Bullous keratopathy | Bullous keratopathy (disorder)
+BMGC_DS03492,BMG_DS004889,45382000,Folds AND/OR rupture of Bowman's membrane,,,,,DOID:11552,Bowman's membrane folds or rupture,C0155115,,,MONDO:0001310,Bowman's membrane folds or rupture,Folds AND/OR rupture of Bowman's membrane | Folds AND/OR rupture of Bowman's membrane (disorder) | Folds AND/OR rupture of Bowman membrane
+BMGC_DS03493,BMG_DS004890,111521006,Corneal degeneration,,9A78.4,Corneal degeneration,H18.4,DOID:1237,corneal degeneration,C0155118,,,MONDO:0001515,corneal degeneration,Corneal degeneration | Corneal degeneration (disorder)
+BMGC_DS03494,BMG_DS004891,2055003,Recurrent erosion of cornea,,,,H18.83,DOID:11541,recurrent corneal erosion,C0155119,,,,,Recurrent erosion of cornea | Recurrent erosion of cornea (disorder) | Recurrent erosion syndrome | Recurrent corneal erosion
+BMGC_DS03495,BMG_DS004892,,"Corneal Dystrophy, Band-Shaped",,,,,DOID:11164,band keratopathy,C0155120,C562399,217500,MONDO:0009016,band keratopathy,
+BMGC_DS03496,BMG_DS004894,72620002,Nodular degeneration of cornea,,,,,DOID:2879,nodular degeneration of cornea,C0155122,,,MONDO:0002449,nodular degeneration of cornea,Nodular degeneration of cornea | Nodular degeneration of cornea (disorder)
+BMGC_DS03497,BMG_DS004895,89182000,Peripheral degeneration of cornea,,,,,DOID:14507,peripheral degeneration of cornea,C0155123,,,MONDO:0001983,peripheral degeneration of cornea,Peripheral degeneration of cornea | Peripheral degeneration of cornea (disorder)
+BMGC_DS03498,BMG_DS004897,,"Familial Amyloid Polyneuropathy, Type V","Amyloid Neuropathies, Familial",,,,,,C0155127,D028227,,MONDO:0004686,lattice corneal dystrophy,
+BMGC_DS03499,BMG_DS004898,193844000,"Keratoconus, stable condition",,,,,DOID:10428,stable condition keratoconus,C0155131,,,MONDO:0001030,"keratoconus, stable condition","Keratoconus, stable condition | Keratoconus, stable condition (disorder)"
+BMGC_DS03500,BMG_DS004899,14748007,Corneal ectasia,,,,H18.71,DOID:1436,corneal ectasia,C0155135,,MTHU061000,MONDO:0001950,corneal ectasia,Corneal ectasia | Corneal ectasia (disorder) | Ectasia of cornea
+BMGC_DS03501,BMG_DS004901,9824006,"Serous conjunctivitis, except viral",,,,H10.23,DOID:11197,serous conjunctivitis except viral,C0155142,,,MONDO:0001219,serous conjunctivitis except viral,"Serous conjunctivitis, except viral | Serous conjunctivitis, except viral (disorder)"
+BMGC_DS03502,BMG_DS004902,41308008,Acute follicular conjunctivitis,,,,H10.01,DOID:11219,conjunctival folliculosis,C0155143,,,MONDO:0001228,conjunctival folliculosis,Acute follicular conjunctivitis | Conjunctival folliculosis | Acute follicular conjunctivitis (disorder)
+BMGC_DS03503,BMG_DS004903,193862009;72115001;267643002,Pseudomembranous conjunctivitis,,,,H10.22,DOID:11190,pseudomembranous conjunctivitis,C0155144,,,MONDO:0001217,pseudomembranous conjunctivitis,Conjunctivitis: [pseudomembranous] or [membranous] | Membranous conjunctivitis | Pseudomembranous conjunctivitis | Conjunctivitis: [pseudomembranous] or [membranous] (disorder) | Pseudomembranous conjunctivitis | Pseudomembranous conjunctivitis (disorder)
+BMGC_DS03504,BMG_DS004904,155163007;73762008,Chronic conjunctivitis,,9A60.Z,"Conjunctivitis, unspecified",H10.4,DOID:2475,chronic conjunctivitis,C0155145,,,MONDO:0002314,chronic conjunctivitis,Chronic conjunctivitis | Chronic conjunctivitis (disorder)
+BMGC_DS03505,BMG_DS004905,193866007;8211008,Simple chronic conjunctivitis,,,,H10.42,DOID:9512,simple chronic conjunctivitis,C0155146,,,MONDO:0004811,simple chronic conjunctivitis,Simple chronic conjunctivitis | Simple chronic conjunctivitis (disorder)
+BMGC_DS03506,BMG_DS004906,39429002,Chronic follicular conjunctivitis,,,,H10.43,DOID:13326,chronic follicular conjunctivitis,C0155147,,,MONDO:0001685,chronic follicular conjunctivitis,Chronic follicular conjunctivitis | Chronic follicular conjunctivitis (disorder)
+BMGC_DS03507,BMG_DS004907,13816006,Parasitic conjunctivitis,,,,,DOID:13341,parasitic conjunctivitis,C0155148,,,MONDO:0001690,parasitic conjunctivitis,Parasitic conjunctivitis | Parasitic conjunctivitis (disorder)
+BMGC_DS03508,BMG_DS004908,69397000;193871000,Angular blepharoconjunctivitis,,,,H10.52,DOID:2455,angular blepharoconjunctivitis,C0155149,,,MONDO:0002306,angular blepharoconjunctivitis,Angular blepharoconjunctivitis | Angular blepharoconjunctivitis (disorder)
+BMGC_DS03509,BMG_DS004909,10813004;193872007,Contact blepharoconjunctivitis,,,,H10.53,DOID:13999,contact blepharoconjunctivitis,C0155150,,,MONDO:0001853,contact blepharoconjunctivitis,Contact blepharoconjunctivitis | Contact blepharoconjunctivitis (disorder)
+BMGC_DS03510,BMG_DS004910,10128002,Rosacea conjunctivitis,,,,H10.82,DOID:9709,rosacea conjunctivitis,C0155152,,,MONDO:0004856,rosacea conjunctivitis,Rosacea conjunctivitis | Rosacea conjunctivitis (disorder)
+BMGC_DS03511,BMG_DS004913,193881001,"Peripheral pterygium, progressive",,,,,DOID:13474,progressive peripheral pterygium,C0155155,,,MONDO:0001723,progressive peripheral pterygium,"Peripheral pterygium, progressive | Peripheral pterygium, progressive (disorder)"
+BMGC_DS03512,BMG_DS004914,,,,,,,DOID:13473,central pterygium,C0155156,,,MONDO:0001722,central pterygium,
+BMGC_DS03513,BMG_DS004915,193883003;41564009,Double pterygium,,,,,DOID:10525,double pterygium,C0155157,,,MONDO:0001054,double pterygium,Double pterygium | Double pterygium (disorder)
+BMGC_DS03514,BMG_DS004917,40787005,Conjunctival degeneration,,,,,DOID:10139,conjunctival degeneration,C0155160,,,MONDO:0000949,conjunctival degeneration,Conjunctival degeneration | Conjunctival degeneration (disorder)
+BMGC_DS03515,BMG_DS004918,66139007,Pseudopterygium,,,,,DOID:11028,pseudopterygium,C0155161,,,MONDO:0001178,pseudopterygium,Pseudopterygium | Pseudopterygium (disorder)
+BMGC_DS03516,BMG_DS004919,,,,,,,DOID:11988,conjunctival concretion,C0155162,,,MONDO:0001412,conjunctival concretion,
+BMGC_DS03517,BMG_DS004920,267645009;66081003,Conjunctival pigmentation,,,,,DOID:12304,conjunctival pigmentation,C0155163,,,MONDO:0006537,conjunctival pigmentation,Conjunctival pigmentation | Conjunctival pigmentation (finding) | Conjunctival pigmentation | Conjunctival pigmentation (disorder)
+BMGC_DS03518,BMG_DS004924,359610006;781682005;76849009,Ocular hyperemia,,,,,DOID:1248,ocular hyperemia,C0155169,,,MONDO:0001534,ocular hyperemia,Hyperemia of eyes | Ocular hyperaemia | Ocular hyperemia | Hyperaemia of eyes | Ocular hyperemia (disorder) | Bloodshot eye | Hyperaemia of eye | Hyperemia of eye | Hyperemia of eye (finding) | Ocular hyperemia | Ocular hyperaemia | Hyperemia of conjunctiva | Hyperaemia of conjunctiva | Hyperemia of conjunctiva (disorder)
+BMGC_DS03519,BMG_DS004927,91662004,Ulcerative blepharitis,,,,H01.01,DOID:9483,ulcerative blepharitis,C0155173,,,MONDO:0004799,ulcerative blepharitis,Ulcerative blepharitis | Ulcerative blepharitis (disorder)
+BMGC_DS03520,BMG_DS004928,58912008,Squamous blepharitis,,,,H01.02,DOID:13825,squamous blepharitis,C0155174,,,MONDO:0001813,squamous blepharitis,Squamous blepharitis | Squamous blepharitis (disorder) | Anterior lid margin disease | Anterior squamous lid disease
+BMGC_DS03521,BMG_DS004930,111524003,Noninfectious dermatosis of eyelid,,,,,DOID:1894,noninfectious dermatoses of eyelid,C0155176,,,MONDO:0002137,noninfectious dermatoses of eyelid,Noninfectious dermatosis of eyelid | Noninfectious dermatosis of eyelid (disorder) | Non-infectious dermatosis of eyelid
+BMGC_DS03522,BMG_DS004931,36259009,Eczematous dermatitis of eyelid,,,,H01.13,DOID:1893,eczematous dermatitis of eyelid,C0155177,,,MONDO:0002136,eczematous dermatitis of eyelid,Eczematous dermatitis of eyelid | Eczema of eyelid | Eyelid eczema | Eczematous dermatitis of eyelid (disorder)
+BMGC_DS03523,BMG_DS004932,402249007,Allergic contact dermatitis of eyelid,,,,,DOID:1895,allergic contact dermatitis of eyelid,C0155178,,,MONDO:0002138,allergic contact dermatitis of eyelid,Allergic contact dermatitis of eyelid (disorder) | Allergic contact dermatitis of eyelid
+BMGC_DS03524,BMG_DS004933,55846006,Xeroderma of eyelid,,,,H01.14,DOID:9140,xeroderma of eyelid,C0155179,,,MONDO:0004718,xeroderma of eyelid,Xeroderma of eyelid | Xeroderma of eyelid (disorder)
+BMGC_DS03525,BMG_DS004934,79291003,Discoid lupus erythematosus of eyelid,,,,H01.12,DOID:9076,discoid lupus erythematosus of eyelid,C0155180,,,MONDO:0004706,discoid lupus erythematosus of eyelid,Discoid lupus erythematosus of eyelid | Discoid lupus erythematosus of eyelid (disorder) | Discoid lupus erythematosus eyelid | Discoid lupus eyelid
+BMGC_DS03526,BMG_DS004935,,,,,,,DOID:9423,blepharitis,C0155181,,,,,
+BMGC_DS03527,BMG_DS004936,193922006,Parasitic eyelid infestation,,,,,DOID:13823,parasitic eyelid infestation,C0155183,,,MONDO:0001812,parasitic eyelid infestation,Parasitic eyelid infestation | Parasitic eyelid infestation (disorder)
+BMGC_DS03528,BMG_DS004938,55408009,Senile entropion,,,,,DOID:12836,senile entropion,C0155188,,,MONDO:0001591,senile entropion,Senile entropion | Senile entropion (disorder) | Age-related entropion | Involutional entropion
+BMGC_DS03529,BMG_DS004939,38683003,Mechanical entropion,,,,,DOID:13112,mechanical entropion,C0155189,,,MONDO:0001636,mechanical entropion,Mechanical entropion | Mechanical entropion (disorder)
+BMGC_DS03530,BMG_DS004940,20828000,Spastic entropion,,,,,DOID:12395,spastic entropion,C0155190,,,MONDO:0001518,spastic entropion,Spastic entropion | Spastic entropion (disorder)
+BMGC_DS03531,BMG_DS004941,67383002,Cicatricial entropion,,,,,DOID:13113,cicatricial entropion,C0155191,,,MONDO:0001637,cicatricial entropion,Cicatricial entropion | Cicatricial entropion (disorder)
+BMGC_DS03532,BMG_DS004942,71659009,Senile ectropion,,,,,DOID:13356,senile ectropion,C0155193,,,MONDO:0001695,senile ectropion,Senile ectropion | Senile ectropion (disorder) | Involutional ectropion | Age-related ectropion
+BMGC_DS03533,BMG_DS004943,45020000,Mechanical ectropion,,,,,DOID:1569,mechanical ectropion,C0155194,,,MONDO:0002042,mechanical ectropion,Mechanical ectropion | Mechanical ectropion (disorder)
+BMGC_DS03534,BMG_DS004944,80846000,Spastic ectropion,,,,,DOID:1571,spastic ectropion,C0155195,,,MONDO:0002044,spastic ectropion,Spastic ectropion | Spastic ectropion (disorder)
+BMGC_DS03535,BMG_DS004945,28914006,Cicatricial ectropion,,,,,DOID:12782,cicatricial ectropion,C0155196,,MTHU037244,MONDO:0001582,cicatricial ectropion,Cicatricial ectropion | Cicatricial ectropion (disorder)
+BMGC_DS03536,BMG_DS004946,,Paralytic Lagophthalmos,Lagophthalmos,,,,DOID:12958,paralytic lagophthalmos,C0155197,D000092164,,MONDO:0001603,paralytic lagophthalmos,
+BMGC_DS03537,BMG_DS004947,193939008;21783006,Mechanical lagophthalmos,,,,H02.22,DOID:13037,mechanical lagophthalmos,C0155198,,,MONDO:0001622,mechanical lagophthalmos,Mechanical lagophthalmos | Mechanical lagophthalmos (disorder)
+BMGC_DS03538,BMG_DS004948,,Cicatricial Lagophthalmos,Lagophthalmos,,,,DOID:13038,cicatricial lagophthalmos,C0155199,D000092164,,MONDO:0001623,cicatricial lagophthalmos,
+BMGC_DS03539,BMG_DS004952,,Hyperpigmentation of Eyelids,,,,,DOID:10122,hyperpigmentation of eyelid,C0155211,C562400,145100,MONDO:0007769,hyperpigmentation of eyelid,
+BMGC_DS03540,BMG_DS004953,193958004;68210006,Hypopigmentation of eyelid,,,,H02.73,DOID:11668,hypopigmentation of eyelid,C0155212,,,MONDO:0006561,eyelid hypopigmentation,Hypopigmentation of eyelid | Hypopigmentation of eyelid (disorder)
+BMGC_DS03541,BMG_DS004954,79830009,Hypertrichosis of eyelid,,,,H02.86,DOID:11669,hypertrichosis of eyelid,C0155213,,,MONDO:0001334,hypertrichosis of eyelid,Hypertrichosis of eyelid | Hypertrichosis of eyelid (disorder)
+BMGC_DS03542,BMG_DS004955,193959007;70738004,Hypotrichosis of eyelid,,,,H02.72,DOID:11671,hypotrichosis of eyelid,C0155214,,,MONDO:0001335,hypotrichosis of eyelid,Hypotrichosis of eyelid | Hypotrichosis of eyelid (disorder)
+BMGC_DS03543,BMG_DS004958,86927009,Dacryoadenitis,Dacryocystitis,9A1Z,"Disorders of lacrimal apparatus, unspecified",H04.0,DOID:950,dacryoadenitis,C0155223,D003607,,MONDO:0004804,dacryoadenitis,Dacryoadenitis | Dacryadenitis | Dacryoadenitis (disorder)
+BMGC_DS03544,BMG_DS004959,4760008,Chronic dacryoadenitis,,,,H04.02,DOID:949,chronic dacryoadenitis,C0155224,,,MONDO:0004800,chronic dacryoadenitis,Chronic dacryoadenitis | Chronic dacryoadenitis (disorder)
+BMGC_DS03545,BMG_DS004961,193978007;17093002,Primary lacrimal atrophy,,,,,DOID:1399,primary lacrimal atrophy,C0155229,,,MONDO:0001851,primary lacrimal atrophy,Primary lacrimal atrophy | Primary lacrimal atrophy (disorder)
+BMGC_DS03546,BMG_DS004962,84777002,Dislocation of lacrimal gland,,,,,DOID:11134,prolapse of lacrimal gland,C0155231,,,MONDO:0001203,prolapse of lacrimal gland,Dislocation of lacrimal gland | Dislocation of lacrimal gland (disorder) | Prolapse of lacrimal gland
+BMGC_DS03547,BMG_DS004963,193984005;31788005,Epiphora due to excess lacrimation,,,,H04.21,DOID:14244,epiphora due to excess lacrimation,C0155233,,,MONDO:0001918,epiphora due to excess lacrimation,Epiphora due to excess lacrimation | Epiphora due to excess lacrimation (disorder)
+BMGC_DS03548,BMG_DS004964,85042000,Epiphora due to insufficient drainage,,,,H04.22,DOID:13756,epiphora due to insufficient drainage,C0155234,,,MONDO:0001792,epiphora due to insufficient drainage,Epiphora due to insufficient drainage | Epiphora due to insufficient drainage (disorder)
+BMGC_DS03549,BMG_DS004965,193986007;25470000,Acute dacryocystitis,,,,H04.32,DOID:12996,acute dacryocystitis,C0155237,,,MONDO:0001610,acute dacryocystitis,(Acute and unspecified inflammation of lacrimal passages) or (acute dacryocystitis) | Dacryocystitis - acute | Acute dacryocystitis | Acute and unspecified inflammation of lacrimal passages | (Acute and unspecified inflammation of lacrimal passages) or (acute dacryocystitis) (disorder) | Acute dacryocystitis | Acute dacryocystitis (disorder)
+BMGC_DS03550,BMG_DS004966,64324003;193988008,Phlegmonous dacryocystitis,,,,H04.31,DOID:12997,Phlegmonous dacryocystitis,C0155238,,,MONDO:0001611,phlegmonous dacryocystitis,Phlegmonous dacryocystitis | Cellulitis of lacrimal sac | Phlegmonous dacryocystitis (disorder) | Phlegmonous dacryocystitis | Phlegmonous dacryocystitis (disorder)
+BMGC_DS03551,BMG_DS004967,193990009;787179008,Chronic inflammation of lacrimal passage,,,,,DOID:9935,chronic inflammation of lacrimal passage,C0155239,,,MONDO:0004923,chronic inflammation of lacrimal passage,Chronic inflammation of lacrimal passage (& [dacryocystitis]) | Dacryocystitis - chronic | Chronic inflammation of lacrimal passage | Chronic dacryocystitis | Chronic inflammation of lacrimal passage (& [dacryocystitis]) (disorder) | Chronic inflammation of lacrimal drainage structure (disorder) | Chronic inflammation of lacrimal drainage structure | Chronic inflammation of lacrimal passage
+BMGC_DS03552,BMG_DS004968,26479009,Chronic lacrimal canaliculitis,,,,H04.42,DOID:9936,chronic canaliculitis,C0155240,,,MONDO:0004924,chronic canaliculitis,Chronic lacrimal canaliculitis | Chronic lacrimal canaliculitis (disorder) | Chronic canaliculitis
+BMGC_DS03553,BMG_DS004969,42758002,Lacrimal mucocele,,,,,DOID:9939,dacryocystocele,C0155241,,,MONDO:0004927,dacryocystocele,Lacrimal mucocele | Dacryocele | Dacryocystocele | Lacrimal mucocele (disorder) | Lacrimal sac mucocele | Lacrimal mucocoele
+BMGC_DS03554,BMG_DS004970,28244003,Eversion of lacrimal punctum,,,,H04.52,DOID:13651,eversion of lacrimal punctum,C0155243,,,MONDO:0001766,eversion of lacrimal punctum,Eversion of lacrimal punctum | Eversion of lacrimal punctum (disorder)
+BMGC_DS03555,BMG_DS004971,74783009,Stenosis of lacrimal punctum,,,,H04.56,DOID:13653,stenosis of lacrimal punctum,C0155244,,,MONDO:0001767,stenosis of lacrimal punctum,Stenosis of lacrimal punctum | Stenosis of lacrimal punctum (disorder) | Punctal stenosis
+BMGC_DS03556,BMG_DS004972,,,,,,,DOID:13654,stenosis of lacrimal passage,C0155245,,,MONDO:0001768,stenosis of lacrimal passage,
+BMGC_DS03557,BMG_DS004973,,,,,,,DOID:3096,stenosis of lacrimal sac,C0155246,,,MONDO:0002511,stenosis of lacrimal sac,
+BMGC_DS03558,BMG_DS004975,,,,,,,DOID:13655,acquired tear duct stenosis,C0155248,,,MONDO:0001769,acquired tear duct stenosis,
+BMGC_DS03559,BMG_DS004978,194001006;417563003,Lacrimal passage granuloma,,,,,DOID:10174,lacrimal passage granuloma,C0155253,,,MONDO:0000957,lacrimal passage granuloma,Lacrimal passage granuloma | Lacrimal passage granuloma (disorder) | Granuloma of lacrimal passage | Lacrimal sac granuloma | Lacrimal passage granuloma | Lacrimal sac granuloma (disorder)
+BMGC_DS03560,BMG_DS004979,,,,,,,DOID:11230,acute orbital inflammation,C0155256,,,MONDO:0001230,acute orbital inflammation,
+BMGC_DS03561,BMG_DS004980,65974003,Orbital periostitis,,,,,DOID:11231,orbital periostitis,C0155257,,,MONDO:0001231,orbital periostitis,Orbital periostitis | Orbital periostitis (disorder) | Orbital osteoperiostitis
+BMGC_DS03562,BMG_DS004981,65875003,Orbital osteomyelitis,,,,,DOID:11232,orbital osteomyelitis,C0155258,,,MONDO:0001232,orbital osteomyelitis,Orbital osteomyelitis | Orbital osteomyelitis (disorder)
+BMGC_DS03563,BMG_DS004982,8976003,Tenonitis,,,,,DOID:11233,orbital tenonitis,C0155259,,,MONDO:0001233,orbital tenonitis,Tenonitis | Tenonitis (disorder) | Orbital tenonitis
+BMGC_DS03564,BMG_DS004983,44729001,Chronic inflammation of orbit,,,,,DOID:1397,chronic orbital inflammation,C0155261,,,MONDO:0001849,chronic orbital inflammation,Chronic inflammation of orbit | Chronic inflammation of orbit (disorder) | Chronic orbital inflammation
+BMGC_DS03565,BMG_DS004984,72776003;194008000,Orbital granuloma,,,,,DOID:10499,orbital granuloma,C0155262,,,MONDO:0001048,orbital granuloma,Orbital granuloma | Orbital granuloma (disorder)
+BMGC_DS03566,BMG_DS004986,53061005;415717005;276177000,Endocrine exophthalmos,,,,,DOID:12359,endocrine exophthalmos,C0155264,,,MONDO:0001509,endocrine exophthalmos,Endocrine exophthalmos | Endocrine exophthalmos (disorder) | Dysthyroid exophthalmos | Thyroid-associated ophthalmopathy | Ophthalmic Graves disease | Dysthyroid eye disease | Endocrine orbitopathy | Graves' ophthalmopathy | Thyroid orbitopathy | Graves ophthalmopathy | Thyroid eye disease with exophthalmos (disorder) | Thyroid eye disease with exophthalmos | Dysthyroid exophthalmos | Endocrine exophthalmos | Thyroid eye disease | Thyroid eye disease (disorder) | Thyroid ophthalmopathy | Graves' ophthalmopathy | Graves ophthalmopathy | Endocrine orbitopathy | Dysthyroid eye disease | Graves eye disease | Graves' eye disease | Ophthalmic Graves disease | Thyroid orbitopathy | Thyroid-associated ophthalmopathy | Endocrine ophthalmopathy | Endocrine exophthalmos | Dysthyroid orbitopathy
+BMGC_DS03567,BMG_DS004987,19885005,Thyrotoxic exophthalmos,,,,,DOID:12362,thyrotoxic exophthalmos,C0155265,,,MONDO:0001511,thyrotoxic exophthalmos,Thyrotoxic exophthalmos | Thyrotoxic exophthalmos (disorder)
+BMGC_DS03568,BMG_DS004989,194015008;89907009,Constant exophthalmos,,,,H05.24,DOID:9945,constant exophthalmos,C0155267,,,MONDO:0004929,constant exophthalmos,Constant exophthalmos | Constant exophthalmos (disorder)
+BMGC_DS03569,BMG_DS004990,49774006,Intermittent exophthalmos,,,,H05.25,DOID:12363,intermittent proptosis,C0155270,,,MONDO:0001512,intermittent proptosis,Intermittent exophthalmos | Intermittent exophthalmos (disorder) | Intermittent proptosis
+BMGC_DS03570,BMG_DS004991,2284002,Pulsating exophthalmos,,,,H05.26,DOID:12364,pulsating exophthalmos,C0155271,,,MONDO:0001513,pulsating exophthalmos,Pulsating exophthalmos | Pulsating exophthalmos (disorder)
+BMGC_DS03571,BMG_DS004992,48747004,Lateral displacement of eye,,,,,DOID:12360,lateral displacement of eye,C0155272,,,MONDO:0001510,lateral displacement of eye,Lateral displacement of globe | Lateral displacement of eye | Lateral displacement of eye (disorder)
+BMGC_DS03572,BMG_DS004997,31021007,Orbital cyst,,,,,DOID:14233,orbital cyst,C0155285,,,MONDO:0001915,orbital cyst,Orbital cyst | Cyst of orbit | Cyst of orbit (disorder)
+BMGC_DS03573,BMG_DS004998,57130002,Myopathy of extraocular muscles,,,,H05.82,DOID:929,myopathy of extraocular muscle,C0155286,,,MONDO:0004746,myopathy of extraocular muscle,Myopathy of extraocular muscles | Myopathy of extraocular muscles (disorder) | Extraocular myopathy
+BMGC_DS03574,BMG_DS004999,54767005,Disorder of visual pathways,,,,,DOID:1393,visual pathway disease,C0155287,,,MONDO:0001834,visual pathway disorder,Disorder of visual pathways | Disorder of afferent visual pathways | Disorder of optic nerve and visual pathway | Disorder of visual pathways (disorder)
+BMGC_DS03575,BMG_DS005000,,Papilledema Associated with Increased Intracranial Pressure,Papilledema,,,,DOID:10175,optic papillitis,C0155288,D010211,,,,
+BMGC_DS03576,BMG_DS005002,21098003,Primary optic atrophy,,,,H47.21,DOID:10627,primary optic atrophy,C0155291,,,MONDO:0001084,primary optic atrophy,Primary optic atrophy | Primary optic atrophy (disorder)
+BMGC_DS03577,BMG_DS005005,111527005;194044005,Partial optic atrophy,,,,,DOID:10631,partial optic atrophy,C0155295,,,MONDO:0001086,partial optic atrophy,Partial optic atrophy | Partial optic atrophy (disorder) | Temporal pallor - optic disc | Partial optic atrophy | (Partial optic atrophy) or (temporal pallor - optic disc)
+BMGC_DS03578,BMG_DS005007,19148004,Crater-like holes of optic disc,,,,,DOID:13295,crater-like holes of optic disc,C0155298,,,,,Crater-like holes of optic disc | Crater-like holes of optic disc (disorder)
+BMGC_DS03579,BMG_DS005008,,,,,,,DOID:11975,coloboma of optic nerve,C0155299,,120430,MONDO:0007354,coloboma of optic nerve,
+BMGC_DS03580,BMG_DS005009,57138009,Pseudopapilledema,,,,,DOID:1392,pseudopapilledema,C0155300,C562401,177800;MTHU006800,MONDO:0008331,obsolete pseudopapilledema,Pseudopapilledema | Pseudopapilloedema | Pseudopapilledema (disorder) | Crowded optic disc
+BMGC_DS03581,BMG_DS005010,51604006,Acute retrobulbar neuritis,,,,,DOID:14155,acute retrobulbar neuritis,C0155301,,,MONDO:0001895,acute retrobulbar neuritis,Acute retrobulbar neuritis | Acute retrobulbar neuritis (disorder) | Acute retrobulbar optic neuritis
+BMGC_DS03582,BMG_DS005011,82108004,Nutritional optic neuropathy,,,,H46.2,DOID:1209,nutritional optic neuropathy,C0155302,,,MONDO:0001431,toxic or nutritional optic neuropathy,Nutritional optic neuropathy | Disorder of optic nerve due to nutritional deficiency (disorder) | Disorder of optic nerve due to nutritional deficiency
+BMGC_DS03583,BMG_DS005012,,Toxic Optic Neuropathy,Toxic Optic Neuropathy,,,,DOID:13329,toxic optic neuropathy,C0155303,D000081028,,MONDO:0001688,toxic optic neuropathy,
+BMGC_DS03584,BMG_DS005013,,"Optic Neuropathy, Ischemic","Optic Neuropathy, Ischemic",,,,DOID:12010,anterior ischemic optic neuropathy,C0155305,D018917,,,,
+BMGC_DS03585,BMG_DS005014,70476006,Optic chiasm disorder,,,,,DOID:5655,chiasmal syndrome,C0155307,,,MONDO:0003568,disorder of optic chiasm,Chiasma syndrome | Optic chiasm disorder | Optic chiasm disorder (disorder)
+BMGC_DS03586,BMG_DS005021,,"Blindness, Cortical","Blindness, Cortical",,,,DOID:11831,cortical blindness,C0155320,D019575,,MONDO:0001385,cortical blindness,
+BMGC_DS03587,BMG_DS005035,194112008,Esotropia with accommodative compensation,,,,,DOID:9839,accommodative esotropia,C0155336,,,MONDO:0004895,accommodative esotropia,Esotropia with accommodative compensation | Esotropia with accommodative compensation (disorder)
+BMGC_DS03588,BMG_DS005036,78097002,Total ophthalmoplegia,,,,,DOID:539,ophthalmoplegia,C0155338,,,,,Total ophthalmoplegia | Total ophthalmoplegia (disorder)
+BMGC_DS03589,BMG_DS005037,,Brown Tendon Sheath Syndrome,Ocular Motility Disorders,,,,DOID:10235,Brown's tendon sheath syndrome,C0155339,D015835,616407,MONDO:0014624,Brown syndrome,
+BMGC_DS03590,BMG_DS005039,194141004;31166000;815008,Episcleritis periodica fugax,,,,H15.11,DOID:12124,episcleritis periodica fugax,C0155351,,,MONDO:0001439,episcleritis periodica fugax,Episcleritis periodica fugax | Episcleritis periodica fugax (disorder) | Episcleritis | Episcleritis (disorder) | Episcleritis periodica fugax
+BMGC_DS03591,BMG_DS005040,70558001,Nodular episcleritis,,,,H15.12,DOID:728,nodular episcleritis,C0155352,,,MONDO:0004170,nodular episcleritis,Nodular episcleritis | Nodular episcleritis (disorder)
+BMGC_DS03592,BMG_DS005041,63454000,Anterior scleritis,,,,H15.01,DOID:13794,anterior scleritis,C0155353,,MTHU053348,MONDO:0001804,anterior scleritis,Anterior scleritis | Anterior scleritis (disorder)
+BMGC_DS03593,BMG_DS005042,26664005,Scleromalacia perforans,,,,H15.05,DOID:14230,scleromalacia perforans,C0155354,,,MONDO:0001914,scleromalacia perforans,Scleromalacia perforans | Scleromalacia perforans (disorder) | Anterior necrotizing scleritis without inflammation | Anterior necrotising scleritis without inflammation
+BMGC_DS03594,BMG_DS005043,42574005,Scleritis with corneal involvement,,,,H15.04,DOID:13861,scleroperikeratitis,C0155355,,,MONDO:0001816,scleroperikeratitis,Scleritis with corneal involvement | Scleroperikeratitis | Scleritis with corneal involvement (disorder)
+BMGC_DS03595,BMG_DS005044,91612009,Brawny scleritis,,,,H15.02,DOID:14287,brawny scleritis,C0155356,,,MONDO:0001936,brawny scleritis,Brawny scleritis | Brawny scleritis (disorder) | Diffuse scleritis
+BMGC_DS03596,BMG_DS005045,194144007;49429000;267660007,Posterior scleritis,,,,H15.03,DOID:13676,posterior scleritis,C0155357,,MTHU053352,MONDO:0001774,posterior scleritis,(Posterior scleritis) or (sclerotenonitis) | Posterior scleritis | Sclerotenonitis | (Posterior scleritis) or (sclerotenonitis) (disorder) | Posterior scleritis | Posterior scleritis (disorder)
+BMGC_DS03597,BMG_DS005047,111534007,Scleral staphyloma,,,,,DOID:11595,scleral staphyloma,C0155359,,,,,Scleral staphyloma | Scleral staphyloma (disorder)
+BMGC_DS03598,BMG_DS005048,87819007,Staphyloma posticum,,,,H15.83,DOID:13789,staphyloma posticum,C0155360,,,MONDO:0001801,staphyloma posticum,Staphyloma posticum | Staphyloma posticum (disorder) | Posterior staphyloma | Partial scleral ectasia | Posterior scleral staphyloma
+BMGC_DS03599,BMG_DS005049,82146006,Equatorial staphyloma,,,,H15.81,DOID:13788,equatorial staphyloma,C0155361,,,MONDO:0001800,equatorial staphyloma,Equatorial staphyloma | Equatorial staphyloma (disorder) | Equatorial scleral staphyloma
+BMGC_DS03600,BMG_DS005050,21946002,Localized anterior staphyloma,,,,H15.82,DOID:13787,localized anterior staphyloma,C0155362,,,MONDO:0001799,localized anterior staphyloma,Localized anterior staphyloma | Localised anterior staphyloma | Anterior localised staphyloma | Anterior localized staphyloma | Localized anterior staphyloma (disorder)
+BMGC_DS03601,BMG_DS005051,5299007,Ring staphyloma,,,,H15.85,DOID:11594,ring staphyloma,C0155363,,,MONDO:0001320,ring staphyloma,Ring staphyloma | Ring staphyloma (disorder)
+BMGC_DS03602,BMG_DS005053,60189009,Vitreous degeneration,,,,H43.81,DOID:11816,vitreous syneresis,C0155366,,MTHU049388,MONDO:0001377,vitreous syneresis,Vitreous degeneration | Vitreous degeneration (disorder)
+BMGC_DS03603,BMG_DS005057,194160006;37283009,Anterior dislocation of lens,,,,H27.12,DOID:2460,anterior dislocation of lens,C0155372,,,MONDO:0002310,anterior dislocation of lens,Anterior dislocation of lens | Anterior dislocation of lens (disorder)
+BMGC_DS03604,BMG_DS005058,194161005;14169000,Posterior dislocation of lens,,,,H27.13,DOID:14199,posterior dislocation of lens,C0155373,,,MONDO:0001906,posterior dislocation of lens,Posterior dislocation of lens | Posterior dislocation of lens (disorder)
+BMGC_DS03605,BMG_DS005059,21011008,Atypical Argyll-Robertson pupil (disorder),,,,,DOID:14523,Argyll Robertson pupil,C0155375,,,,,Atypical Argyll-Robertson pupil | Nonsyphilitic Argyll-Robertson phenomenon | Atypical Argyll-Robertson pupil (disorder)
+BMGC_DS03606,BMG_DS005060,,Other anomalies of pupillary function,,,,H57.09,DOID:11518,abnormal pupillary function,C0155376,,,,,
+BMGC_DS03607,BMG_DS005061,46888001,Nystagmus associated with disorder of the vestibular system,,,,,DOID:14070,vestibular nystagmus,C0155379,,,,,Vestibular nystagmus | Nystagmus associated with disorder of the vestibular system (disorder) | Nystagmus associated with disorder of the vestibular system
+BMGC_DS03608,BMG_DS005062,,Dissociated Nystagmus,"Nystagmus, Pathologic",,,,DOID:13174,dissociated nystagmus,C0155380,D009759,,MONDO:0001655,dissociated nystagmus,
+BMGC_DS03609,BMG_DS005064,,,,,,,DOID:379,external ear disease,C0155388,,,MONDO:0002776,external ear disorder,
+BMGC_DS03610,BMG_DS005065,34129005;155210008,Perichondritis of pinna,,AA04,Perichondritis of external ear,H61.0,DOID:222,perichondritis of auricle,C0155389,,,MONDO:0002246,perichondritis of auricle,Perichondritis of pinna | Perichondritis of auricle | Perichondritis of pinna (disorder) | Perichondritis of pinna | Perichondritis of pinna (disorder)
+BMGC_DS03611,BMG_DS005066,45855004,Acute perichondritis of pinna,,,,,DOID:221,acute perichondritis of pinna,C0155390,,,MONDO:0002240,acute perichondritis of pinna,Acute perichondritis of pinna | Acute perichondritis of pinna (disorder)
+BMGC_DS03612,BMG_DS005067,45431004;194195009,Chronic perichondritis of pinna,,,,,DOID:14243,chronic perichondritis of pinna,C0155391,,,MONDO:0001917,chronic perichondritis of pinna,Chronic perichondritis of pinna | Chronic perichondritis of pinna (disorder) | Chronic pinna perichondritis (& [chondrodermatitis nodularis helicis]) | Chondrodermatitis nodularis helicis | Chronic perichondritis of pinna | Chronic pinna perichondritis | Chronic pinna perichondritis (& [chondrodermatitis nodularis helicis]) (disorder)
+BMGC_DS03613,BMG_DS005068,56663002,Acute infection of pinna,,,,,DOID:10520,acute infection of pinna,C0155392,,,MONDO:0001053,acute infection of pinna,Acute infection of pinna | Acute infection of pinna (disorder)
+BMGC_DS03614,BMG_DS005069,194206006;94146005,Malignant otitis externa,,AA02,Malignant otitis externa,H60.2,DOID:10516,malignant otitis externa,C0155395,,,MONDO:0001050,malignant otitis externa,Malignant otitis externa | Malignant otitis externa (disorder) | Malignant otitis externa | Malignant otitis externa (disorder) | Necrotising otitis externa | Necrotizing otitis externa
+BMGC_DS03615,BMG_DS005070,111898002,Chronic mycotic otitis externa,,,,,DOID:10519,chronic fungal otitis externa,C0155396,,,MONDO:0001052,chronic fungal otitis externa,Chronic mycotic otitis externa | Chronic mycotic otitis externa (disorder) | Chronic fungal otitis externa
+BMGC_DS03616,BMG_DS005072,35247001,Cholesteatoma of external ear,,AA40.2,Cholesteatoma of external auditory canal,H60.4,DOID:9462,cholesteatoma of external ear,C0155398,,,MONDO:0006532,cholesteatoma of external ear,Cholesteatoma of external ear | Cholesteatoma of external ear (disorder)
+BMGC_DS03617,BMG_DS005075,19560007,Exostosis of external ear canal,,,,,,,C0155411,,128300,MONDO:0007498,ear exostoses,Exostosis of external ear canal | Exostosis of external ear canal (disorder) | External auditory canal exostosis | Swimmers exostosis
+BMGC_DS03618,BMG_DS005077,11957006;194240006,Acute serous otitis media,,AA80,Acute serous or mucoid otitis media,H65.0,DOID:11557,acute serous otitis media,C0155415,,,MONDO:0001312,acute serous otitis media,Acute serous otitis media | Acute serous otitis media (disorder) | Acute non-suppurative serous otitis media (disorder) | Acute nonsuppurative serous otitis media | Acute non-suppurative serous otitis media
+BMGC_DS03619,BMG_DS005078,194241005;59275002,Acute allergic serous otitis media,,,,,DOID:11558,acute allergic serous otitis media,C0155418,,,MONDO:0001313,acute allergic serous otitis media,Acute allergic serous otitis media | Acute allergic serous otitis media (disorder)
+BMGC_DS03620,BMG_DS005079,194242003;8326008,Acute allergic mucoid otitis media,,,,,DOID:9735,acute allergic mucoid otitis media,C0155419,,,MONDO:0004864,acute allergic mucoid otitis media,Acute allergic mucoid otitis media | Acute allergic mucoid otitis media (disorder)
+BMGC_DS03621,BMG_DS005080,17866004,Acute allergic sanguineous otitis media,,,,,DOID:3728,acute allergic sanguinous otitis media,C0155420,,,MONDO:0002757,acute allergic sanguinous otitis media,Acute allergic sanguinous otitis media | Acute allergic sanguineous otitis media (disorder) | Acute allergic sanguineous otitis media
+BMGC_DS03622,BMG_DS005081,81564005,Chronic serous otitis media,,AA82,Chronic serous or mucoid otitis media,H65.2,DOID:11181,serous glue ear,C0155421,,,MONDO:0001213,serous glue ear,"Chronic serous otitis media | Simple chronic serous otitis media | Glue ear - serous | Otitis media with effusion - serous | Chronic secretory otitis media, serous | Chronic non-suppurative otitis media with effusion - serous | Chronic serous otitis media (disorder)"
+BMGC_DS03623,BMG_DS005082,270491006;194266009,Eustachian tube salpingitis,,,,,DOID:2000,otosalpingitis,C0155428,,,MONDO:0002172,otosalpingitis,Eustachian tube salpingitis | Eustachian tube salpingitis (disorder) | Otosalpingitis | Eustachian salpingitis | Tubotympanitis | Eustachian tube: [salpingitis] or [catarrh] | Eustachian tube salpingitis | Catarrh - eustachian | Eustachian tube: [salpingitis] or [catarrh] (disorder)
+BMGC_DS03624,BMG_DS005083,194268005,Acute eustachian tube salpingitis,,,,,DOID:10550,acute eustachian salpingitis,C0155429,,,MONDO:0001064,acute eustachian salpingitis,Acute eustachian tube salpingitis | Acute eustachian tube salpingitis (disorder)
+BMGC_DS03625,BMG_DS005084,194269002,Chronic eustachian tube salpingitis,,,,,DOID:1999,chronic eustachian salpingitis,C0155430,,,MONDO:0002170,chronic eustachian salpingitis,Chronic eustachian tube salpingitis | Chronic eustachian tube salpingitis (disorder) | Chronic eustachian salpingitis
+BMGC_DS03626,BMG_DS005087,30280005,Patulous eustachian tube,,,,,DOID:12358,patulous eustachian tube,C0155434,,,MONDO:0001508,patulous eustachian tube,Patulous eustachian tube | Patulous eustachian tube (disorder)
+BMGC_DS03627,BMG_DS005088,,,,,,,DOID:9739,eustachian tube disease,C0155435,,,,,
+BMGC_DS03628,BMG_DS005089,,,,,,,DOID:10435,purulent acute otitis media,C0155439,,,,,
+BMGC_DS03629,BMG_DS005090,87665008,Chronic tubotympanic suppurative otitis media,,AA91.0,Chronic tubotympanic suppurative otitis media,H66.1,DOID:14435,chronic tubotympanic suppurative otitis media,C0155440,,,MONDO:0001964,chronic tubotympanic suppurative otitis media,Chronic tubotympanic suppurative otitis media | Chronic tubotympanic suppurative otitis media (disorder) | Chronic suppurative otitis media - tubotympanic
+BMGC_DS03630,BMG_DS005091,41954005,Chronic atticoantral suppurative otitis media,,AA91.1,Chronic atticoantral suppurative otitis media,H66.2,DOID:14248,chronic atticoantral disease,C0155441,,,MONDO:0001921,chronic atticoantral disease,Chronic atticoantral suppurative otitis media | Chronic atticoantral disease with posterior AND/OR superior marginal perforation of ear drum | Persistent mucosal disease with posterior AND/OR superior marginal perforation of ear drum | Chronic atticoantral suppurative otitis media (disorder) | Chronic suppurative otitis media - atticoantral
+BMGC_DS03631,BMG_DS005095,155233009;267760001;34997001,Petrositis,Petrositis,AB11.2,Petrositis,H70.2,DOID:10755,petrositis,C0155448,D059270,,MONDO:0001109,petrositis,Petrositis &/or other mastoiditis | Other mastoiditis | Petrositis | Petrositis &/or other mastoiditis (disorder) | Petrositis &/or other mastoiditis | Petrositis | Other mastoiditis | Petrositis &/or other mastoiditis (disorder) | Petrositis | Inflammation of petrous bone | Petrositis (disorder)
+BMGC_DS03632,BMG_DS005096,51211002,Acute petrositis,,,,H70.21,DOID:10755,petrositis,C0155449,,,,,Acute petrositis | Acute petrositis (disorder)
+BMGC_DS03633,BMG_DS005097,28593007,Chronic petrositis,,,,H70.22,DOID:10755,petrositis,C0155450,,,,,Chronic petrositis | Chronic petrositis (disorder)
+BMGC_DS03634,BMG_DS005100,297009,Acute myringitis,,AB14,Acute myringitis,H73.0,DOID:13790,acute tympanitis,C0155460,,,MONDO:0001802,acute tympanitis,Acute myringitis | Acute tympanitis | Acute myringitis (disorder)
+BMGC_DS03635,BMG_DS005101,33528003,Bullous myringitis,,,,H73.01,DOID:13791,myringitis bullosa hemorrhagica,C0155461,,,MONDO:0001803,myringitis bullosa hemorrhagica,Bullous myringitis | Myringitis bullosa hemorrhagica | Myringitis bullosa haemorrhagica | Bullous myringitis (disorder) | Myringitis bullosa
+BMGC_DS03636,BMG_DS005106,38645004,Atrophic flaccid tympanic membrane,,,,H73.81,DOID:5781,atrophic flaccid tympanic membrane,C0155470,,,MONDO:0003647,atrophic flaccid tympanic membrane,Atrophic flaccid tympanic membrane | Atrophic flaccid tympanic membrane (disorder)
+BMGC_DS03637,BMG_DS005107,194323000;72052003,Atrophic nonflaccid tympanic membrane,,,,H73.82,DOID:12546,atrophic nonflaccid tympanic membrane,C0155471,,,MONDO:0001547,atrophic nonflaccid tympanic membrane,Atrophic nonflaccid tympanic membrane | Atrophic nonflaccid tympanic membrane (disorder)
+BMGC_DS03638,BMG_DS005109,111540000,Tympanosclerosis involving other combination of structures,,,,,DOID:1214,tympanosclerosis,C0155477,,,,,Tympanosclerosis involving other combination of structures | Tympanosclerosis involving other combination of structures (disorder)
+BMGC_DS03639,BMG_DS005110,7699004,Adhesive middle ear disease,,AB17,Adhesive middle ear disease,H74.1,DOID:11235,adhesive otitis media,C0155478,,,MONDO:0001234,adhesive otitis media,Adhesive middle ear disease | Chronic adhesive otitis media | Fibrotic adhesive otitis media | Adhesive otitis media | Adhesive middle ear disease (disorder)
+BMGC_DS03640,BMG_DS005112,,,,,,,DOID:11129,dislocation of ear ossicle,C0155487,,,,,
+BMGC_DS03641,BMG_DS005113,,,,,,,DOID:11783,necrosis of ear ossicle,C0155488,,,,,
+BMGC_DS03642,BMG_DS005114,38708003,Cholesteatoma of attic,,,,H71.0,DOID:10963,cholesteatoma of attic,C0155489,,,MONDO:0006531,cholesteatoma of attic,Cholesteatoma of attic | Cholesteatoma of attic (disorder)
+BMGC_DS03643,BMG_DS005115,,Middle Ear Cholesteatoma,"Cholesteatoma, Middle Ear",,,,DOID:10964,cholesteatoma of middle ear,C0155490,D018424,,MONDO:0006533,cholesteatoma of middle ear,
+BMGC_DS03644,BMG_DS005117,,,,,,,DOID:10852,middle ear cholesterol granuloma,C0155492,,,MONDO:0001141,middle ear cholesterol granuloma,
+BMGC_DS03645,BMG_DS005119,194348002,Active cochleovestibular Ménière's disease,,,,,DOID:13490,active cochleovestibular Meniere's disease,C0155496,,,MONDO:0001727,active cochleovestibular Meniere disease,Active cochleovestibular Meniere's disease | Active cochleovestibular Ménière's disease (disorder) | Active cochleovestibular Ménière's disease | Active cochleovestibular Ménière disease
+BMGC_DS03646,BMG_DS005120,194349005,Active cochlear Ménière's disease,,,,,DOID:13492,active cochlear Meniere's disease,C0155497,,,MONDO:0001729,active cochlear Meniere disease,Active cochlear Meniere's disease | Active cochlear Ménière's disease (disorder) | Active cochlear Ménière's disease | Active cochlear Ménière disease
+BMGC_DS03647,BMG_DS005121,194350005,Active vestibular Ménière's disease,,,,,DOID:13491,active vestibular Meniere's disease,C0155498,,,MONDO:0001728,active vestibular Meniere disease,Active vestibular Meniere's disease | Active vestibular Ménière's disease (disorder) | Active vestibular Ménière's disease | Active vestibular Ménière disease
+BMGC_DS03648,BMG_DS005123,,"Vertigo, Peripheral",Vertigo,,,,,,C0155501,D014717,,MONDO:0004900,peripheral vertigo,
+BMGC_DS03649,BMG_DS005124,,Benign Paroxysmal Positional Vertigo,Benign Paroxysmal Positional Vertigo,,,,DOID:13941,benign paroxysmal positional vertigo,C0155502,D065635,193007,MONDO:8000018,benign paroxysmal positional vertigo,
+BMGC_DS03650,BMG_DS005125,,Central Nervous System Origin Vertigo,Vertigo,,,,DOID:2479,central nervous system origin vertigo,C0155503,D014717,,MONDO:0002317,central nervous system origin vertigo,
+BMGC_DS03651,BMG_DS005126,41674001,Serous labyrinthitis,,,,,DOID:1467,serous labyrinthitis,C0155504,,,MONDO:0002006,serous labyrinthitis,Serous labyrinthitis | Serous labyrinthitis (disorder)
+BMGC_DS03652,BMG_DS005127,61794006;194364005,Circumscribed labyrinthitis,,,,,DOID:13867,focal labyrinthitis,C0155505,,,MONDO:0001820,focal labyrinthitis,Circumscribed labyrinthitis | Focal labyrinthitis | Circumscribed labyrinthitis (disorder) | Circumscribed labyrinthitis | Circumscribed labyrinthitis (disorder)
+BMGC_DS03653,BMG_DS005128,24817009,Suppurative labyrinthitis,,,,,DOID:13534,purulent labyrinthitis,C0155506,,,MONDO:0001739,purulent labyrinthitis,Suppurative labyrinthitis | Purulent labyrinthitis | Suppurative labyrinthitis (disorder)
+BMGC_DS03654,BMG_DS005129,3344003,Toxic labyrinthitis,,,,,DOID:14081,toxic labyrinthitis,C0155507,,,MONDO:0001874,toxic labyrinthitis,Toxic labyrinthitis | Toxic labyrinthitis (disorder)
+BMGC_DS03655,BMG_DS005130,409711008;34243007,Viral labyrinthitis,,,,,DOID:12357,viral labyrinthitis,C0155508,,,MONDO:0001507,viral labyrinthitis,Viral labyrinthitis (disorder) | Viral labyrinthitis | Viral otitis interna | Viral labyrinthitis | Viral otitis interna | Vestibular neuritis | Vestibular neuronitis | Acute peripheral vestibulopathy | Epidemic neurolabyrinthitis | Epidemic vertigo | Viral labyrinthitis (disorder)
+BMGC_DS03656,BMG_DS005131,5239005,Labyrinthine dysfunction,,AB36,Labyrinthine dysfunction,H83.2;H83.2X,DOID:566,labyrinthine dysfunction,C0155514,,,,,Labyrinthine dysfunction | Labyrinthine dysfunction (disorder)
+BMGC_DS03657,BMG_DS005132,,,,,,,DOID:1777,unilateral hyperactive labyrinth,C0155515,,,MONDO:0002107,unilateral hyperactive labyrinth,
+BMGC_DS03658,BMG_DS005133,194373002,Hyperactive bilateral labyrinthine dysfunction,,,,,DOID:14165,bilateral hyperactive labyrinth,C0155516,,,MONDO:0001897,bilateral hyperactive labyrinth,Hyperactive bilateral labyrinthine dysfunction | Hyperactive bilateral labyrinthine dysfunction (disorder)
+BMGC_DS03659,BMG_DS005134,,,,,,,DOID:9496,unilateral hypoactive labyrinth,C0155517,,,MONDO:0004801,unilateral hypoactive labyrinth,
+BMGC_DS03660,BMG_DS005135,194375009,Hypoactive bilateral labyrinthine dysfunction,,,,,DOID:565,bilateral hypoactive labyrinth,C0155518,,,MONDO:0003567,bilateral hypoactive labyrinth,Hypoactive bilateral labyrinthine dysfunction | Hypoactive bilateral labyrinthine dysfunction (disorder)
+BMGC_DS03661,BMG_DS005136,,,,,,,DOID:1776,labyrinthine unilateral reactive loss,C0155519,,,MONDO:0002106,labyrinthine unilateral reactive loss,
+BMGC_DS03662,BMG_DS005137,,,,,,,DOID:14413,labyrinthine bilateral reactive loss,C0155520,,,MONDO:0001959,labyrinthine bilateral reactive loss,
+BMGC_DS03663,BMG_DS005142,,,,,,,DOID:10261,otorrhea,C0155540,,,MONDO:0000988,discharging ear,
+BMGC_DS03664,BMG_DS005154,194719006;155287003;78069008,Chronic rheumatic pericarditis,,BB21,Chronic rheumatic pericarditis,I09.2,DOID:1869,chronic rheumatic pericarditis,C0155561,,,MONDO:0002133,chronic rheumatic pericarditis,Chronic rheumatic pericarditis | Chronic rheumatic pericarditis (disorder) | Chronic rheumatic pericarditis | Chronic rheumatic heart disease with pericarditis | Rheumatic heart disease with pericarditis | Chronic pericarditis due to rheumatic heart disease (disorder) | Chronic pericarditis due to rheumatic heart disease
+BMGC_DS03665,BMG_DS005155,31085000;155278007,Rheumatic mitral regurgitation,,BB61.0,Rheumatic mitral valve insufficiency,I05.1,DOID:61,mitral valve disease,C0155563,,,,,Rheumatic mitral regurgitation | Rheumatic mitral incompetence | Rheumatic mitral insufficiency | Rheumatic mitral regurgitation (disorder) | Rheumatic mitral regurgitation | Rheumatic mitral regurgitation (disorder)
+BMGC_DS03666,BMG_DS005156,155282009;72011007,Rheumatic aortic stenosis,,BB70.0,Rheumatic aortic valve stenosis,I06.0,DOID:1712,aortic valve stenosis,C0155567,,,,,Rheumatic aortic stenosis | Rheumatic aortic stenosis (disorder)
+BMGC_DS03667,BMG_DS005157,155283004;78031003,Rheumatic aortic regurgitation,,BB71.0,Rheumatic aortic valve insufficiency,I06.1,DOID:57,aortic valve insufficiency,C0155568,,,,,Rheumatic aortic regurgitation | Rheumatic aortic regurgitation (disorder) | Rheumatic aortic regurgitation | Rheumatic aortic incompetence | Rheumatic aortic insufficiency | Rheumatic aortic regurgitation (disorder) | Aortic incompetence - rheumatic
+BMGC_DS03668,BMG_DS005159,18687009,Rheumatic disease of pulmonary valve,,,,I09.89,DOID:5748,rheumatic pulmonary valve disease,C0155579,,,MONDO:0003627,rheumatic pulmonary valve disease,Rheumatic disease of pulmonary valve | Rheumatic pulmonary valve disease | Rheumatic disease of pulmonary valve (disorder)
+BMGC_DS03669,BMG_DS005160,82523003,Congestive rheumatic heart failure,,,,,DOID:14172,rheumatic congestive heart failure,C0155582,,,MONDO:0001899,rheumatic congestive heart failure,Congestive rheumatic heart failure | Congestive rheumatic heart failure (disorder)
+BMGC_DS03670,BMG_DS005161,194758001;1201005,Benign essential hypertension (disorder),,,,,DOID:10913,benign essential hypertension,C0155583,,,MONDO:0001151,benign essential hypertension,Benign essential hypertension | Benign essential hypertension (disorder)
+BMGC_DS03671,BMG_DS005167,65443008,Malignant hypertensive renal disease,,,,,DOID:10177,malignant hypertensive renal disease,C0155593,,,MONDO:0000959,malignant hypertensive renal disease,Malignant hypertensive renal disease | Malignant hypertensive renal disease (disorder)
+BMGC_DS03672,BMG_DS005168,193003,Benign hypertensive renal disease,,,,,DOID:11520,benign hypertensive renal disease,C0155596,,,MONDO:0001304,benign hypertensive renal disease,Benign hypertensive renal disease | Benign hypertensive renal disease (disorder)
+BMGC_DS03673,BMG_DS005173,31992008;155300002,Secondary hypertension,,,,I15,DOID:11130,secondary hypertension,C0155616,,,MONDO:0001200,secondary hypertension,Secondary hypertension | Secondary hypertension (disorder)
+BMGC_DS03674,BMG_DS005174,89242004,Malignant secondary hypertension,,,,,DOID:13731,malignant secondary hypertension,C0155617,,,MONDO:0001785,malignant secondary hypertension,Malignant secondary hypertension | Accelerated secondary hypertension | Malignant secondary hypertension (disorder)
+BMGC_DS03675,BMG_DS005175,44111003;194785008,Benign secondary hypertension,,,,,DOID:13143,benign secondary hypertension,C0155620,,,MONDO:0001646,benign secondary hypertension,Benign secondary hypertension | Benign secondary hypertension (disorder) | Secondary benign hypertension | Secondary benign hypertension | Secondary benign hypertension (disorder) | Benign secondary hypertension
+BMGC_DS03676,BMG_DS005176,,,,,,,DOID:13145,benign renovascular hypertension,C0155621,,,MONDO:0001647,benign renovascular hypertension,
+BMGC_DS03677,BMG_DS005177,155304006;266288001;194796000;57054005,Acute myocardial infarction,,,,I21,DOID:9408,acute myocardial infarction,C0155626,,,MONDO:0004781,acute myocardial infarction,Myocardial infarction (& [acute]) or coronary thrombosis | Coronary thrombosis | Myocardial infarct | Heart attack | Attack - heart | MI - Acute myocardial infarction | MI/Acute myocardial infarction | Acute myocardial infarction | Myocardial infarction (& [acute]) or coronary thrombosis (disorder) | MI/Acute myocardial infarction | Acute myocardial infarction | Coronary thrombosis | Attack - heart | Heart attack | MI - Acute myocardial infarction | Myocardial infarct | Myocardial infarction (& [acute]) or coronary thrombosis | Myocardial infarction (& [acute]) or coronary thrombosis (disorder) | Coronary thrombosis | Thrombosis - coronary | Silent myocardial infarction | MI - Acute myocardial infarction | Heart attack | Cardiac rupture after acute myocardial infarction | Acute myocardial infarction | Attack - heart | Cardiac rupture following myocardial infarction (MI) | MI - acute myocardial infarction | (Myocardial infarction (& [acute] or [silent] or [cardiac rupture following])) or (coronary thrombosis) | (Myocardial infarction (& [acute] or [silent] or [cardiac rupture following])) or (coronary thrombosis) (disorder) | Acute myocardial infarction | Acute myocardial infarction (disorder) | AMI - Acute myocardial infarction
+BMGC_DS03678,BMG_DS005178,70211005,Acute myocardial infarction of anterolateral wall,,,,,DOID:10651,acute anterolateral myocardial infarction,C0155627,,,MONDO:0001090,acute anterolateral myocardial infarction,Acute myocardial infarction of anterolateral wall | Acute myocardial infarction of anterolateral wall (disorder) | Acute anterolateral myocardial infarction
+BMGC_DS03679,BMG_DS005179,,,,,,,DOID:10649,acute inferolateral myocardial infarction,C0155636,,,,,
+BMGC_DS03680,BMG_DS005180,,,,,,,DOID:10648,acute inferoposterior infarction,C0155640,,,,,
+BMGC_DS03681,BMG_DS005181,,,,,,,DOID:9407,strictly posterior acute myocardial infarction,C0155652,,,,,
+BMGC_DS03682,BMG_DS005182,,,,,,,DOID:10266,subendocardial infarction acute myocardial infarction,C0155655,,,,,
+BMGC_DS03683,BMG_DS005184,155324005;194880009;49584005;67189007,Acute pulmonary heart disease,,,,,DOID:8514;DOID:8517,acute cor pulmonale | acute pulmonary heart disease,C0155671,,,MONDO:0004598,acute cor pulmonale,Acute pulmonary heart disease | Acute pulmonary heart disease (disorder) | Acute cor pulmonale | Acute cor pulmonale (disorder) | Acute pulmonary heart disease
+BMGC_DS03684,BMG_DS005185,,,,,,,DOID:12326,chronic pulmonary heart disease,C0155673,,,,,
+BMGC_DS03685,BMG_DS005187,155333007;194902002;15555002,Acute pericarditis,,,,I30,,,C0155679,,,,,Acute pericarditis | Acute pericarditis (disorder) | (Acute pericarditis) or (acute pericardial effusion) | Acute pericarditis | Pericardial effusion - acute | (Acute pericarditis) or (acute pericardial effusion) (disorder)
+BMGC_DS03686,BMG_DS005191,155336004;46701001,Acute myocarditis,,,,I40,DOID:3951,acute myocarditis,C0155686,,,MONDO:0002815,acute myocarditis,Acute myocarditis | Acute myocarditis (disorder)
+BMGC_DS03687,BMG_DS005192,194954007;266238009,Isolated (Fiedler's) myocarditis,,,,,DOID:10778,fiedler's myocarditis,C0155689,,,MONDO:0001113,Fiedler's myocarditis,Myocarditis: [isolated - Fiedler's] or [giant cell] | Isolated (Fiedler's) myocarditis | Giant cell myocarditis | Myocarditis: [isolated - Fiedler's] or [giant cell] (disorder) | Isolated (Fiedler's) myocarditis | Isolated (Fiedler's) myocarditis (disorder)
+BMGC_DS03688,BMG_DS005193,64043005,Septic myocarditis,,BC42.1,Infectious myocarditis,I40.0,DOID:10779,septic myocarditis,C0155690,,,,,Bacterial myocarditis | Septic myocarditis | Bacterial myocarditis (disorder)
+BMGC_DS03689,BMG_DS005194,31993003,Toxic myocarditis,,,,,DOID:9694,toxic myocarditis,C0155691,,,MONDO:0004851,toxic myocarditis,Toxic myocarditis | Toxic myocarditis (disorder) | Acute toxic disorder of myocardium
+BMGC_DS03690,BMG_DS005198,,,,,,,DOID:3978,extrinsic cardiomyopathy,C0155699,,,,,
+BMGC_DS03691,BMG_DS005199,28189009,Mobitz type II atrioventricular block,,,,,DOID:11312,Mobitz type II atrioventricular block,C0155700,,,MONDO:0001261,Mobitz type II atrioventricular block,Mobitz type II atrioventricular block | Mobitz type II incomplete atrioventricular block | Second degree Mobitz type II incomplete atrioventricular block | Mobitz type II atrioventricular block (disorder)
+BMGC_DS03692,BMG_DS005200,4973001;266245009;195044001,Left bundle branch hemiblock,,,,,DOID:10272,left bundle branch hemiblock,C0155702,,,,,Left bundle branch hemiblock | Left bundle branch hemiblock (disorder) | Left bundle branch [block] or [hemiblock] | Left bundle branch block | Left bundle branch hemiblock | Left bundle branch [block] or [hemiblock] (disorder)
+BMGC_DS03693,BMG_DS005201,46319007,Right bundle branch block AND left posterior fascicular block,,,,,DOID:13209,right bundle branch block,C0155704,,,,,Right bundle branch block AND left posterior fascicular block | Right bundle branch block AND left posterior fascicular block (disorder) | RBBB - Right bundle branch block with left posterior fascicular block | Right bundle branch block with left posterior fascicular block
+BMGC_DS03694,BMG_DS005205,,,,,,,DOID:11299,vertebral artery occlusion,C0155724,,,,,
+BMGC_DS03695,BMG_DS005206,,Occlusion and stenosis of unspecified precerebral artery,,BD55,Asymptomatic stenosis of intracranial or extracranial artery,I65.9,DOID:5976,occlusion precerebral artery,C0155727,,,,,
+BMGC_DS03696,BMG_DS005208,81817003,Atherosclerosis of aorta,,BD40.1,Atherosclerosis of aorta,I70.0,DOID:10230,aortic atherosclerosis,C0155733,,,MONDO:0000980,aortic atherosclerosis,Atherosclerosis of aorta | Atherosclerosis of aorta (disorder) | Atherosclerotic aorta
+BMGC_DS03697,BMG_DS005209,45281005,Atherosclerosis of renal artery,,BD40.2,Atherosclerosis of renal artery,I70.1,DOID:14092,renal artery atheroma,C0155734,,,MONDO:0001876,renal artery atheroma,Atherosclerosis of renal artery | Atherosclerosis of renal artery (disorder) | Renal artery atheroma | Renal artery atherosclerosis | Atherosclerosis renal artery
+BMGC_DS03698,BMG_DS005219,58729003,Disease of capillaries,,,,,DOID:1271,capillary disease,C0155765,,,MONDO:0001574,capillary disorder,Capillary disease | Capillary disorder | Microangiopathy | Disorder of capillaries (disorder) | Disorder of capillaries
+BMGC_DS03699,BMG_DS005221,840713005,Phlebitis and thrombophlebitis of iliac vein,,,,I80.21,DOID:10880,iliac vein thrombophlebitis,C0155772,,,,,Phlebitis and thrombophlebitis of iliac vein | Phlebitis and thrombophlebitis of iliac vein (disorder)
+BMGC_DS03700,BMG_DS005222,,,,,,,DOID:11695,portal vein thrombosis,C0155773,,,MONDO:0001339,portal vein thrombosis,
+BMGC_DS03701,BMG_DS005223,,,,,,,DOID:866,vein disease,C0155774,,,,,
+BMGC_DS03702,BMG_DS005228,,,,,,,DOID:9745,perianal hematoma,C0155784,,,MONDO:0004871,perianal hematoma,
+BMGC_DS03703,BMG_DS005230,236067006;17709002,Bleeding esophageal varices,,,,,DOID:112,esophageal varix,C0155789,,,MONDO:0021645,esophageal varices with bleeding,Bleeding esophageal varices | Bleeding oesophageal varices | Bleeding oesophageal varices (disorder) | Bleeding esophageal varices | Esophageal varices with hemorrhage | Bleeding oesophageal varices | Oesophageal varices with haemorrhage | Bleeding esophageal varices (disorder) | Oesophageal varices with bleeding | BOV - Bleeding oesophageal varices | Esophageal varices with bleeding | BOV - Bleeding esophageal varices
+BMGC_DS03704,BMG_DS005231,,,,,,,DOID:112,esophageal varix,C0155791,,,,,
+BMGC_DS03705,BMG_DS005232,,,,,,,DOID:112,esophageal varix,C0155792,,,,,
+BMGC_DS03706,BMG_DS005233,17406005,Varicose veins of pelvis,,,,,DOID:9742,pelvic varices,C0155795,,,MONDO:0004869,pelvic varices,Pelvic varices | Varicose veins of pelvis (disorder) | Varicose veins of pelvis
+BMGC_DS03707,BMG_DS005236,155499007;68272006,Acute maxillary sinusitis,,CA01;XA1R64,Acute sinusitis | Maxillary sinus,J01.0,DOID:2050,acute maxillary sinusitis,C0155804,,,MONDO:0002186,acute maxillary sinusitis,Acute maxillary sinusitis | Acute maxillary sinusitis (disorder) | Acute maxillary sinusitis | Acute antritis | Acute maxillary sinusitis (disorder)
+BMGC_DS03708,BMG_DS005237,155500003;91038008,Acute frontal sinusitis,,XA91G8;CA01,Frontal sinus | Acute sinusitis,J01.1,DOID:14225,acute frontal sinusitis,C0155805,,,MONDO:0001912,acute frontal sinusitis,Acute frontal sinusitis | Acute frontal sinusitis (disorder)
+BMGC_DS03709,BMG_DS005238,67832005,Acute ethmoidal sinusitis,,CA01;XA58F6,Acute sinusitis | Ethmoid sinus,J01.2,DOID:9506,acute ethmoiditis,C0155806,,,MONDO:0004810,acute ethmoiditis,Acute ethmoidal sinusitis | Acute ethmoidal sinusitis (disorder) | Acute ethmoiditis
+BMGC_DS03710,BMG_DS005239,77919000,Acute sphenoidal sinusitis,,CA01;XA4U67,Acute sinusitis | Sphenoid sinus,J01.3,DOID:13046,acute sphenoidal sinusitis,C0155807,,,MONDO:0001624,acute sphenoidal sinusitis,Acute sphenoidal sinusitis | Acute sphenoidal sinusitis (disorder)
+BMGC_DS03711,BMG_DS005242,276443001,Acute laryngitis and/or tracheitis,,,,,DOID:0050148,laryngotracheitis,C0155811,,,,,Acute laryngitis/tracheitis | Acute laryngitis and/or tracheitis (disorder) | Acute laryngitis and/or tracheitis
+BMGC_DS03712,BMG_DS005244,29608009,Acute epiglottitis,,CA06.1,Acute epiglottitis,J05.1,DOID:9398,epiglottitis,C0155814,,,MONDO:0041366,acute epiglottitis,Acute epiglottitis | Acute epiglottitis and supraglottitis | Acute epiglottitis (disorder)
+BMGC_DS03713,BMG_DS005246,55355000,Acute laryngopharyngitis,,CA04,Acute laryngopharyngitis,J06.0,DOID:11195,acute laryngopharyngitis,C0155817,,,MONDO:0001218,acute laryngopharyngitis,Acute laryngopharyngitis | Acute laryngopharyngitis (disorder)
+BMGC_DS03714,BMG_DS005250,195763009,Chronic pharyngitis and nasopharyngitis,,,,,DOID:2275,pharyngitis,C0155824,,,,,Chronic pharyngitis and nasopharyngitis | Chronic pharyngitis and nasopharyngitis (disorder)
+BMGC_DS03715,BMG_DS005252,155524006;47841006,Chronic nasopharyngitis,,CA09.1,Chronic nasopharyngitis,J31.1,DOID:10460,nasopharyngitis,C0155826,,,,,Chronic nasopharyngitis | Chronic nasopharyngitis (disorder)
+BMGC_DS03716,BMG_DS005259,155535001;29951006,Chronic laryngitis,,CA0G,Chronic laryngitis or laryngotracheitis,J37.0,DOID:11797,chronic laryngitis,C0155836,,,MONDO:0001369,chronic laryngitis,Chronic laryngitis | Chronic laryngitis (disorder)
+BMGC_DS03717,BMG_DS005260,83271005,Chronic laryngotracheitis,,CA0G,Chronic laryngitis or laryngotracheitis,J37.1,DOID:0050148,laryngotracheitis,C0155837,,,,,Chronic laryngotracheitis | Chronic laryngotracheitis (disorder)
+BMGC_DS03718,BMG_DS005272,41381004,Pneumonia caused by Pseudomonas,,,,,,,C0155860,,,,,Pseudomonal pneumonia | Pneumonia caused by Pseudomonas | Pneumonia caused by Pseudomonas (disorder)
+BMGC_DS03719,BMG_DS005273,34020007,Streptococcal pneumonia,,,,,,,C0155862,,,MONDO:0005972,streptococcal pneumonia,Streptococcal pneumonia | Pneumonia caused by Streptococcus | Pneumonia caused by Streptococcus (disorder)
+BMGC_DS03720,BMG_DS005275,11389007,Inhalational anthrax,,,,,,,C0155866,,,MONDO:0016595,inhalational anthrax,Woolsorters' disease | Respiratory anthrax | Pulmonary anthrax | Inhalational anthrax (disorder) | Inhalational anthrax
+BMGC_DS03721,BMG_DS005282,233680000;389145006;195968006;16862005,Allergic asthma,,,,,DOID:9415,allergic asthma,C0155877,,,MONDO:0004784,allergic asthma,Allergic asthma | Allergic asthma (disorder) | Allergic asthma (disorder) | Allergic asthma | Asthma: [extrinsic - atopic] or [allergic] or [pollen] or [childhood] or [with hay fever] | Pollen asthma | Allergic asthma | Extrinsic (atopic) asthma | Childhood asthma | Hay fever with asthma | Asthma: [extrinsic - atopic] or [allergic] or [pollen] or [childhood] or [with hay fever] (disorder) | Extrinsic asthma | Atopic asthma | Childhood asthma | Allergic asthma | Allergic atopic asthma | Extrinsic asthma (disorder)
+BMGC_DS03722,BMG_DS005284,266397004;195973000;155576005;8312004;266361008,Intrinsic asthma,,,,,DOID:9360,intrinsic asthma,C0155880,,,MONDO:0004765,intrinsic asthma,Asthma: [intrinsic] or [late onset] | Intrinsic asthma | Late-onset asthma | Late-onset asthma (LOA) | Late onset asthma | LOA - late onset asthma | Asthma: [intrinsic] or [late onset] (disorder) | (Intrinsic asthma) or (late onset asthma) | Late onset asthma | Late-onset asthma | Intrinsic asthma | (Intrinsic asthma) or (late onset asthma) (disorder) | LOA - late onset asthma | Late-onset asthma | Late-onset asthma (LOA) | Intrinsic asthma | Late onset asthma | Asthma: [intrinsic] or [late onset] | Asthma: [intrinsic] or [late onset] (disorder) | Intrinsic asthma | Intrinsic asthma (disorder) | Intrinsic asthma | Non-allergic asthma | Asthma due to internal immunological process | Non-allergic asthma (disorder)
+BMGC_DS03723,BMG_DS005286,25897000,Malt-workers' lung,,,,,DOID:2314,malt worker's lung,C0155888,,,MONDO:0002266,malt worker's lung,Malt-workers' lung | Malt-workers' alveolitis | Malt-workers' lung disease | Malt fever | Malt house workers' cough | Alveolitis due to Aspergillus clavatus AND/OR fumigatus | Malt-workers' lung (disorder) | Malt workers' lung | Malt workers lung | Malt workers' hypersensitivity pneumonitis
+BMGC_DS03724,BMG_DS005287,,Mushroom Worker's Lung,Farmer's Lung,,,,DOID:2708,mushroom workers' lung,C0155889,D005203,,MONDO:0005865,mushroom workers' lung,
+BMGC_DS03725,BMG_DS005288,86638007,Maple-bark strippers' lung,,,,,DOID:8484,maple bark strippers' lung,C0155890,,,MONDO:0004584,maple bark strippers' lung,Maple-bark strippers' lung | Alveolitis due to Cryptostroma corticale | Maple-bark disease | Maple-bark strippers' disease | Maple-bark strippers' lung (disorder) | Maple bark strippers' lung | Maple bark strippers lung | Maple bark strippers' hypersensitivity pneumonitis
+BMGC_DS03726,BMG_DS005289,48347002,Humidifier lung,,,,,DOID:11289,ventilation pneumonitis,C0155891,,,MONDO:0001255,ventilation pneumonitis,Humidifier lung | Air conditioner lung | Ventilation pneumonitis | Humidifier AND/OR air conditioning pneumonitis | Humidifier lung (disorder) | Sauna takers lung | Air-conditioner and humidifier lung | Humidifier hypersensitivity pneumonitis
+BMGC_DS03727,BMG_DS005296,76537003;196102003,Spontaneous tension pneumothorax,,CB21.0,Spontaneous tension pneumothorax,J93.0,DOID:1672,spontaneous tension pneumothorax,C0155907,,,MONDO:0002075,spontaneous tension pneumothorax,Spontaneous tension pneumothorax | Spontaneous tension pneumothorax (disorder)
+BMGC_DS03728,BMG_DS005297,196107009,Abscess of lung and mediastinum,,,,J85,,,C0155908,,,,,Abscess of lung and mediastinum | Abscess of lung and mediastinum (disorder)
+BMGC_DS03729,BMG_DS005300,,Pulmonary Alveolar Microlithiasis,,,,,DOID:12117,pulmonary alveolar microlithiasis,C0155912,C562405,265100,MONDO:0009928,pulmonary alveolar microlithiasis,
+BMGC_DS03730,BMG_DS005301,33325001,Compensatory emphysema,,CB40.4,Compensatory emphysema,J98.3,DOID:10031,compensatory emphysema,C0155918,,,MONDO:0000924,compensatory emphysema,Compensatory emphysema | Compensatory emphysema (disorder)
+BMGC_DS03731,BMG_DS005302,123262009;40541001,Acute pulmonary edema,,,,J81.0,,,C0155919,,,,,Acute pulmonary edema (disorder) | Acute pulmonary edema | Acute pulmonary oedema | Acute pulmonary edema | Acute edema of lung | Acute pulmonary oedema | Acute oedema of lung | Acute pulmonary edema (disorder) | Pulmonary oedema - acute | Pulmonary edema - acute
+BMGC_DS03732,BMG_DS005305,,Tooth Ankylosis,Tooth Ankylosis,,,,DOID:12661,tooth ankylosis,C0155930,D020254,157950,MONDO:0008007,tooth ankylosis,
+BMGC_DS03733,BMG_DS005307,88071000,Acute apical periodontitis of pulpal origin,,DA09.70,Acute apical periodontitis of pulpal origin,K04.4,DOID:11693,acute apical periodontitis,C0155934,,,,,Acute apical periodontitis of pulpal origin | Acute apical periodontitis | Acute apical periodontitis of pulpal origin (disorder)
+BMGC_DS03734,BMG_DS005309,31642005;155643004;234990002,Acute gingivitis,,DA0B.Y,Other specified gingival diseases,K05.0,DOID:3087,gingivitis,C0155937,,,,,Acute gingivitis | Acute gingival inflammation | Acute gingivitis (disorder) | Acute gingivitis | Acute gingivitis (disorder)
+BMGC_DS03735,BMG_DS005320,,,,,,,DOID:14111,median rhomboid glossitis,C0155963,,,MONDO:0001880,median rhomboid glossitis,
+BMGC_DS03736,BMG_DS005321,9491003;196588005;196585008;196586009,Atrophy of tongue papillae,,DA03.2,Atrophy of tongue papillae,K14.4,DOID:1453,atrophic glossitis,C0155964,,,MONDO:0001989,atrophic glossitis,Atrophy of tongue papillae | Smooth atrophic tongue | Atrophic glossitis | Hunter's glossitis | Bald tongue | Glossodynia exfoliativa | Moeller's glossitis | Glazed tongue | Tongue denuded of papillae | Moeller's glossodynia exfoliativa | Atrophy of tongue papillae (disorder) | Atrophy of tongue papillae | Atrophy of tongue papillae (disorder)
+BMGC_DS03737,BMG_DS005322,89748001;155682002;196629007,Acute gastric ulcer with hemorrhage,,DA60.Z,"Gastric ulcer, unspecified",K25.0,,,C0155967,,,,,Acute gastric ulcer with hemorrhage | Acute gastric ulcer with bleeding | Acute gastric ulcer with haemorrhage | Acute gastric ulcer with hemorrhage (disorder) | Bleeding acute gastric ulcer | Acute gastric ulcer with haemorrhage | Acute gastric ulcer with hemorrhage | Acute gastric ulcer with haemorrhage (disorder) | Acute gastric ulcer with haemorrhage | Bleeding acute gastric ulcer | Acute gastric ulcer with hemorrhage | Acute gastric ulcer with hemorrhage (disorder)
+BMGC_DS03738,BMG_DS005324,19850005;266499002;196630002,Acute gastric ulcer with perforation,,DA60.Z,"Gastric ulcer, unspecified",K25.1,,,C0155970,,,,,Acute gastric ulcer with perforation | Acute gastric ulcer with perforation (disorder) | Perforated GU | GU - acute + perforation | Acute gastric ulcer with perforation | Perforated GU (& [acute]) | Perforated GU (& [acute]) (disorder)
+BMGC_DS03739,BMG_DS005334,196709002;63954007,Acute gastrojejunal ulcer with hemorrhage,,DA62.Z,"Anastomotic ulcer, unspecified",K28.0,DOID:10927,gastrojejunal ulcer,C0156042,,,,,Acute gastrojejunal ulcer with hemorrhage | Acute gastrojejunal ulcer with haemorrhage | Acute gastrojejunal ulcer with hemorrhage (disorder) | Acute gastrojejunal ulcer with hemorrhage | Acute gastrojejunal ulcer with haemorrhage | Acute gastrojejunal ulcer with hemorrhage (disorder) | Acute stomal ulcer with haemorrhage | Acute stomal ulcer with hemorrhage
+BMGC_DS03740,BMG_DS005340,155714000;2043009,Alcoholic gastritis,,DA42.80,Alcoholic gastritis,K29.2,DOID:8680,alcoholic gastritis,C0156076,,,MONDO:0004640,alcoholic gastritis,Alcoholic gastritis | Alcoholic gastritis (disorder)
+BMGC_DS03741,BMG_DS005343,52232007,Chronic duodenal ileus,,,,,DOID:13687,chronic duodenal ileus,C0156087,,,MONDO:0001775,chronic duodenal ileus,Chronic duodenal ileus | Chronic duodenal ileus (disorder)
+BMGC_DS03742,BMG_DS005356,56689002,Crohn's disease of small intestine,,DD70.1,Crohn disease of small intestine,K50.0,DOID:0060191;DOID:0060188,gastroduodenal Crohn's disease | jejunoileitis,C0156146,,,MONDO:0005539,small bowel Crohn disease,"Crohn's disease of small intestine | Regional enteritis of small intestine | Regional ileitis of small intestine | Segmental ileitis of small intestine | Crohn's disease of small intestine (disorder) | Crohn disease of small intestine | Crohns disease, small intestine | Granulomatous enteritis | Regional enteritis | RE - regional enteritis | Crohn's regional enteritis"
+BMGC_DS03743,BMG_DS005357,7620006,Crohn's disease of large bowel,,,,,DOID:8778;DOID:0060192,Crohn's colitis | Crohn's disease,C0156147,,,MONDO:0005532,Crohn's colitis,"Crohn's disease of large bowel | Crohn's disease of large bowel (disorder) | Regional enteritis of the large bowel | Crohn disease of large bowel | Crohns disease, large intestine"
+BMGC_DS03744,BMG_DS005362,47812002,Functional diarrhea,,DD9Z,"Functional gastrointestinal disorders, unspecified",K59.1,DOID:11371,functional diarrhea,C0156173,,,MONDO:0001272,functional diarrhea,Functional diarrhea | Functional diarrhoea | Functional diarrhea (disorder)
+BMGC_DS03745,BMG_DS005365,,,,,,,DOID:11014,anorectal stricture,C0156183,,,MONDO:0001177,anorectal stricture,
+BMGC_DS03746,BMG_DS005366,197237004;24557004,Abscess of intestine,,ME24.0,Digestive system abscess,K63.0,,,C0156185,,,,,Abscess of intestine | Abscess of intestine (disorder)
+BMGC_DS03747,BMG_DS005370,34736002,Chronic passive congestion of liver,,DB98.8;XT8W,Passive congestion of liver | Chronic,K76.1,DOID:13739,nutmeg liver,C0156195,,,MONDO:0001788,nutmeg liver,Chronic passive congestion of liver | Nutmeg liver | Chronic passive congestion of liver (disorder)
+BMGC_DS03748,BMG_DS005377,197415009;75726005,Obstruction of gallbladder,,DC10.01,Obstruction of gall bladder,K82.0,DOID:9714,occlusion of gallbladder,C0156214,,,MONDO:0004858,occlusion of gallbladder,Obstruction of gallbladder | Obstruction of gallbladder (disorder)
+BMGC_DS03749,BMG_DS005378,,Other diseases of biliary tract,,,,K83,,,C0156217,,,,,
+BMGC_DS03750,BMG_DS005379,,,,,,,DOID:13409,perforation of bile duct,C0156218,,,MONDO:0001710,perforation of bile duct,
+BMGC_DS03751,BMG_DS005383,197776002;155864003;266555009;37779008,Pyeloureteritis cystica,,,,N28.85,DOID:2743,pyeloureteritis cystica,C0156254,,,MONDO:0002410,pyeloureteritis cystica,(Pyeloureteritis cystica) or (ureteritis cystica) or (infestation of renal pelvis with ureter) | Ureteritis cystica | Pyeloureteritis cystica | Infestation of renal pelvis with ureter | (Pyeloureteritis cystica) or (ureteritis cystica) or (infestation of renal pelvis with ureter) (disorder) | Pyeloureteritis cystica | Pyeloureteritis cystica (disorder) | Pyeloureteritis cystica | Ureteritis cystica | Pyelitis cystica | Pyeloureteritis cystica (disorder)
+BMGC_DS03752,BMG_DS005384,197792007;197796005;266622009;155867005;266556005,Calculus of kidney and ureter,,,,N20,DOID:585,nephrolithiasis,C0156257,,,,,Kidney calculus | Urinary calculus | Calculus of kidney and ureter | Urinary calculus (& [kidney &/or ureter) | Urinary calculus (& [kidney &/or ureter) (disorder) | Calculus of kidney and ureter | Calculus of kidney and ureter (disorder) | Calculus kidney/ureter | Kidney/ureter calculus | Urinary calculus | Calculus of kidney and ureter | Stone - kidney/ureter | Kidney stone | Renal stone | Urinary calculus (& [kidney &/or ureter]) | Urinary calculus (& [kidney &/or ureter]) (disorder) | Urinary calculus (& [kidney &/or ureter]) | Calculus of kidney and ureter | Urinary calculus | Kidney stone | Renal stone | Kidney/ureter calculus | Calculus kidney/ureter | Stone - kidney/ureter | Urinary calculus (& [kidney &/or ureter]) (disorder) | Calculus of kidney with calculus of ureter | Calculus of kidney and ureter | Calculus of kidney and ureter (disorder)
+BMGC_DS03753,BMG_DS005386,197800004;88531004,Hypertrophy of kidney,,,,N28.81,DOID:9622,kidney hypertrophy,C0156259,,,MONDO:0004841,kidney hypertrophy,Hypertrophy of kidney | Hypertrophy of kidney (disorder)
+BMGC_DS03754,BMG_DS005387,,,,,,,DOID:3508,stricture or kinking of ureter,C0156261,,,,,
+BMGC_DS03755,BMG_DS005388,79509009,Calculus of lower urinary tract,,,,N21,DOID:9590,lower urinary tract calculus,C0156264,,,MONDO:0004828,lower urinary tract calculus,Calculus of lower urinary tract | Calculus of lower urinary tract (disorder) | Lower urinary tract calculus
+BMGC_DS03756,BMG_DS005389,18109005,Calculus in diverticulum of urinary bladder,,,,,DOID:11354,stone in bladder diverticulum,C0156265,,,MONDO:0001270,stone in bladder diverticulum,Calculus in diverticulum of bladder | Calculus of bladder diverticulum | Stone in bladder diverticulum | Diverticulum of bladder with calculus | Calculus in diverticulum of urinary bladder (disorder) | Calculus in diverticulum of urinary bladder
+BMGC_DS03757,BMG_DS005391,197839008,Other chronic cystitis,,GC00.1;XT8W,Infectious cystitis | Chronic,N30.2,DOID:1680,chronic cystitis,C0156268,,,,,Other chronic cystitis | Other chronic cystitis (disorder)
+BMGC_DS03758,BMG_DS005392,11251000,Radiation cystitis,,,,,DOID:7127,radiation cystitis,C0156270,,,MONDO:0004112,radiation cystitis,Irradiation cystitis | Radiation cystitis | Cystitis caused by radiation | Cystitis caused by radiation (disorder)
+BMGC_DS03759,BMG_DS005393,197858004,Other disorders of bladder,,,,N32,,,C0156271,,,,,Other disorders of bladder | Other disorders of bladder (disorder)
+BMGC_DS03760,BMG_DS005394,,,,,,,DOID:11353,bladder diverticulum,C0156273,,109820,MONDO:0007197,bladder diverticulum,
+BMGC_DS03761,BMG_DS005395,197899005;67277002,Urethral abscess,,GC02.0,Urethral abscess,N34.0,DOID:9877,urethral gland abscess,C0156278,,,,,Urethral abscess | Urethral and periurethral abscess | Periurethral &/or urethral abscess | Periurethral &/or urethral abscess (disorder) | Urethral abscess | Urethral abscess (disorder)
+BMGC_DS03762,BMG_DS005396,31273004,Urethral syndrome,,,,,DOID:13498,urethral syndrome,C0156279,,,MONDO:0001730,urethral syndrome,Urethral syndrome | Urethral syndrome (disorder)
+BMGC_DS03763,BMG_DS005397,,,,,,,DOID:13658,infective urethral stricture,C0156282,,,,,
+BMGC_DS03764,BMG_DS005398,,,,,,,DOID:9339,urethral false passage,C0156286,,,MONDO:0004760,urethral false passage,
+BMGC_DS03765,BMG_DS005401,67685000,Prostatocystitis,,GA91.2,Prostatocystitis,N41.3,DOID:12355,prostatocystitis,C0156291,,,MONDO:0001506,prostatocystitis,Prostatocystitis | Prostatocystitis (disorder)
+BMGC_DS03766,BMG_DS005404,29524003,Atrophy of prostate,,,,,DOID:2301,atrophy of prostate,C0156296,,,,,Atrophy of prostate | Atrophy of prostate (disorder) | Atrophic prostate | Prostate atrophy
+BMGC_DS03767,BMG_DS005409,17585008;155938008;249242001,Atrophy of testis,,GB03,Atrophy of testis,N50.0,DOID:11994,atrophy of testis,C0156312,,,MONDO:0001415,atrophy of testis,Atrophy of testis | Testicular atrophy | Atrophic testicle | Atrophy of testis (disorder) | Atrophy of testis | Atrophy of testis (disorder)
+BMGC_DS03768,BMG_DS005411,234107009;7864001,Chylocele of tunica vaginalis,,,,,DOID:10835,chylocele of tunica vaginalis,C0156315,,,MONDO:0001136,chylocele of tunica vaginalis,Chylocele | Chylocele (disorder) | Scrotal chylocele | Chylocele of tunica vaginalis | Chylocoele of tunica vaginalis | Chylocele of tunica vaginalis | Chylocele of tunica vaginalis (disorder) | Chylocoele of tunica vaginalis
+BMGC_DS03769,BMG_DS005412,,,,,,,DOID:12333,male genital organ stricture,C0156316,,,MONDO:0001496,male genital organ stricture,
+BMGC_DS03770,BMG_DS005413,29070004,Fibrosclerosis of breast,,GB20.0,Fibrocystic change of breast,N60.3,DOID:10353,fibrosclerosis of breast,C0156318,,,MONDO:0006118,breast fibrosis,Fibrosclerosis of breast | Fibrosclerosis of breast (disorder)
+BMGC_DS03771,BMG_DS005416,21381006,Fat necrosis of breast,,GB23.2,Fat necrosis of breast,N64.1,DOID:10691,fat necrosis of breast,C0156321,,,MONDO:0001101,fat necrosis of breast,Fat necrosis of breast | Fat necrosis of breast (disorder)
+BMGC_DS03772,BMG_DS005418,155969007;198134002;266581008,Acute salpingo-oophoritis,,,,,DOID:10971,acute salpingo-oophoritis,C0156327,,,MONDO:0001171,acute salpingo-oophoritis,Acute salpingo-oophoritis | Acute salpingo-oophoritis (disorder) | Acute salpingo-oophoritis | Acute salpingitis and oophoritis | Acute salpingo-oophoritis (disorder)
+BMGC_DS03773,BMG_DS005419,198142001,Chronic salpingo-oophoritis,,,,,DOID:12265,chronic salpingo-oophoritis,C0156328,,,MONDO:0001474,chronic salpingo-oophoritis,Chronic salpingo-oophoritis | Chronic salpingo-oophoritis (disorder) | Chronic salpingitis and oophoritis
+BMGC_DS03774,BMG_DS005424,198230004,Ulceration of vulva associated with another disorder,,,,,DOID:12566,ulceration of vulva,C0156340,,,,,Ulceration of vulva associated with another disorder (disorder) | Ulceration of vulva associated with another disorder
+BMGC_DS03775,BMG_DS005425,198250000;31007005;266589005,Endometriosis of ovary,,GA10.Z,Endometriosis of unspecified site,N80.1,DOID:11432,endometriosis of ovary,C0156344,,,MONDO:0006337,ovarian endometriosis,Endometriosis of ovary (& [chocolate cyst]) | Chocolate cyst of ovary | Endometriosis of ovary | Endometriosis of ovary (& [chocolate cyst]) (disorder) | Endometriosis of ovary | Endometriosis of ovary (disorder)
+BMGC_DS03776,BMG_DS005426,198251001,Endometriosis of pelvic peritoneum,,GA10.C2,Endometriosis of pelvic peritoneum,N80.3,DOID:11429,endometriosis of pelvic peritoneum,C0156345,,,MONDO:0001285,endometriosis of pelvic peritoneum,Endometriosis of pelvic peritoneum | Endometriosis of pelvic peritoneum (disorder)
+BMGC_DS03777,BMG_DS005427,198253003,Endometriosis of rectovaginal septum and vagina,,GA10.B5,Deep ovarian endometriosis,N80.4,DOID:11431,endometriosis of rectovaginal septum and vagina,C0156346,,,MONDO:0001288,endometriosis of rectovaginal septum and vagina,Endometriosis of rectovaginal septum and vagina | Endometriosis of rectovaginal septum and vagina (disorder)
+BMGC_DS03778,BMG_DS005428,5562006,Endometriosis of intestine,,GA10.C1,Endometriosis of intestine,N80.5,DOID:11428,endometriosis of intestine,C0156347,,,MONDO:0001284,endometriosis of intestine,Endometriosis of intestine | Endometriosis of intestine (disorder)
+BMGC_DS03779,BMG_DS005429,53913001,Endometriosis in scar of skin,,,,,DOID:11430,endometriosis in scar of skin,C0156348,,,MONDO:0001287,endometriosis in cutaneous scar,Endometriosis in scar of skin | Endometriosis in scar of skin (disorder) | Scar endometriosis
+BMGC_DS03780,BMG_DS005431,,,,,,,DOID:13050,corpus luteum cyst,C0156361,,,,,
+BMGC_DS03781,BMG_DS005434,,,,,,,DOID:9042,polyp of corpus uteri,C0156369,,,MONDO:0004701,uterine polyp,
+BMGC_DS03782,BMG_DS005435,53518003;198315005,Chronic subinvolution of uterus,,,,,DOID:13811,chronic subinvolution of uterus,C0156370,,,MONDO:0001808,chronic subinvolution of uterus,Chronic subinvolution of uterus | Chronic subinvolution of uterus (disorder)
+BMGC_DS03783,BMG_DS005440,,,,,,,DOID:8920,leukoplakia of vagina,C0156385,,,MONDO:0004679,leukoplakia of vagina,
+BMGC_DS03784,BMG_DS005442,82614005;198382004;248861000,Atrophy of vulva,,GA1Z,"Noninflammatory disorders of female genital tract, unspecified",N90.5,DOID:14275,atrophic vulva,C0156393,,,,,Atrophy of vulva | Atrophy of vulva (disorder) | Atrophic vulva | Atrophic vulvitis | Atrophic vulva (disorder) | Atrophy of vulva
+BMGC_DS03785,BMG_DS005447,52441000;156054004,Postmenopausal atrophic vaginitis,,GA30.2,Postmenopausal atrophic vaginitis,N95.2,DOID:11968,postmenopausal atrophic vaginitis,C0156409,,,MONDO:0001410,postmenopausal atrophic vaginitis,Senile atrophic vaginitis | Postmenopausal atrophic vaginitis | Atrophic vaginitis | Senile vaginitis | Atrophic vaginitis (disorder) | Postmenopausal atrophic vaginitis | Postmenopausal atrophic vaginitis (disorder)
+BMGC_DS03786,BMG_DS005450,,,,,,,DOID:13589,female infertility of uterine origin,C0156416,,,MONDO:0001753,female infertility of uterine origin,
+BMGC_DS03787,BMG_DS005457,,,,,,,,,C0156543,,,MONDO:0041526,pregnancy disorder with abortive outcome,
+BMGC_DS03788,BMG_DS005460,,,,,,,DOID:1677,low implantation of placenta,C0156617,,,MONDO:0002077,low implantation of placenta,
+BMGC_DS03789,BMG_DS005461,,,,,,,DOID:10590,mild pre-eclampsia,C0156664,,,,,
+BMGC_DS03790,BMG_DS005462,,,,,,,DOID:13129,severe pre-eclampsia,C0156669,,,,,
+BMGC_DS03791,BMG_DS005469,,,,,,,DOID:10556,supine hypotensive syndrome,C0157456,,,,,
+BMGC_DS03792,BMG_DS005471,,,,,,,DOID:8512,puerperal pulmonary embolism,C0157540,,,MONDO:0004594,puerperal pulmonary embolism,
+BMGC_DS03793,BMG_DS005487,41174002;156318008;200696002,Acute lymphadenitis,,,,L04,DOID:1602,lymphadenitis,C0157705,,,,,Acute adenitis | Acute lymphadenitis | Acute lymphadenitis (disorder) | Acute lymphadenitis | Acute lymphadenitis (disorder) | Acute cervical adenitis | Acute adenitis | Acute lymphadenitis | Acute abscess lymph node | Acute: [lymphadenitis] or [abscess lymph node] or [cervical adenitis] | Acute: [lymphadenitis] or [abscess lymph node] or [cervical adenitis] (disorder)
+BMGC_DS03794,BMG_DS005491,76092003,Benign mucous membrane pemphigoid with ocular involvement,,,,,DOID:11656,cicatricial pemphigoid,C0157721,,,,,Benign mucous membrane pemphigoid with ocular involvement | Benign mucous membrane pemphigoid with ocular involvement (disorder)
+BMGC_DS03795,BMG_DS005494,156423009;19429009,Chronic skin ulcer,,,,,DOID:8549,chronic ulcer of skin,C0157738,,,MONDO:0004605,chronic ulcer of skin,Chronic skin ulcer | Chronic skin ulcer (disorder) | Chronic ulcer of skin | Chronic skin ulcer | Chronic ulcer of skin (disorder)
+BMGC_DS03796,BMG_DS005496,,Vibratory Urticaria,Chronic Inducible Urticaria,,,,DOID:1554,vibratory urticaria,C0157743,D000094482,,MONDO:0006618,vibratory urticaria,
+BMGC_DS03797,BMG_DS005497,396233005;48548006;201455003;371412008,Arthropathy associated with infection,,,,,DOID:381,arthropathy,C0157749,,,,,Arthropathy associated with infection (disorder) | Arthropathy associated with infection | Infectious arthropathy | Arthropathy related to infection | Arthropathy associated with infection | Infection-associated arthritis | Infectious arthropathy | Arthropathy related to infection | Arthropathy associated with infection (disorder) | Arthropathy associated with infection | Infection-associated arthritis | Arthropathy related to infection | Arthropathy related to infection (disorder) | Arthropathy associated with infection (disorder) | Arthropathy associated with infection | Arthropathy related to infection | Infection-associated arthritis
+BMGC_DS03798,BMG_DS005498,62918002,Arthropathy in Behcet's syndrome,,,,,DOID:1670,Behcet's syndrome arthropathy,C0157770,,,MONDO:0002074,Behcet syndrome arthropathy,Arthropathy in Behcet's syndrome | Behcet's syndrome arthropathy | Seronegative arthritis secondary to Behcet's syndrome | Arthropathy in Behcet's syndrome (disorder) | Arthropathy in Behcet syndrome
+BMGC_DS03799,BMG_DS005500,428437005,Infective arthritis of shoulder region,,,,,DOID:813,septic arthritis,C0157843,,,,,Infective arthritis of shoulder region (disorder) | Infective arthritis of shoulder region
+BMGC_DS03800,BMG_DS005501,,,,,,,DOID:813,septic arthritis,C0157844,,,,,
+BMGC_DS03801,BMG_DS005502,,,,,,,DOID:813,septic arthritis,C0157845,,,,,
+BMGC_DS03802,BMG_DS005503,,,,,,,DOID:813,septic arthritis,C0157846,,,,,
+BMGC_DS03803,BMG_DS005504,,,,,,,DOID:813,septic arthritis,C0157847,,,,,
+BMGC_DS03804,BMG_DS005505,,,,,,,DOID:813,septic arthritis,C0157848,,,,,
+BMGC_DS03805,BMG_DS005506,,,,,,,DOID:813,septic arthritis,C0157849,,,,,
+BMGC_DS03806,BMG_DS005507,201625003,Chondrocalcinosis due to dicalcium phosphate crystals,,,,,DOID:1156,chondrocalcinosis,C0157852,,,,,Chondrocalcinosis caused by dicalcium phosphate crystals | Chondrocalcinosis caused by dicalcium phosphate crystals (disorder)
+BMGC_DS03807,BMG_DS005510,75822003;201798003;16024431000119108,Acute polyarticular juvenile rheumatoid arthritis,,,,,DOID:676,juvenile rheumatoid arthritis,C0157916,,,,,Acute polyarticular juvenile rheumatoid arthritis | Acute juvenile rheumatoid arthritis | Acute polyarticular juvenile rheumatoid arthritis (disorder) | Polyarticular juvenile rheumatoid arthritis | Acute polyarticular juvenile rheumatoid arthritis | Acute polyarticular juvenile rheumatoid arthritis (disorder) | Acute polyarticular juvenile idiopathic arthritis (disorder) | Acute polyarticular juvenile idiopathic arthritis | Acute polyarticular juvenile rheumatoid arthritis
+BMGC_DS03808,BMG_DS005511,74391003,Pauciarticular juvenile rheumatoid arthritis,,FA24.1,Juvenile idiopathic polyarthritis,M08.4,DOID:676,juvenile rheumatoid arthritis,C0157917,,,,,Pauciarticular juvenile rheumatoid arthritis | JCA - Pauciarticular onset juvenile chronic arthritis | Pauciarticular onset juvenile arthritis | Pauciarticular onset juvenile chronic arthritis | Pauciarticular juvenile rheumatoid arthritis (disorder)
+BMGC_DS03809,BMG_DS005512,201799006;83793004,Monoarticular juvenile rheumatoid arthritis,,,,,DOID:676,juvenile rheumatoid arthritis,C0157918,,,,,Monarticular juvenile rheumatoid arthritis | Monarticular juvenile rheumatoid arthritis (disorder) | Monoarticular juvenile rheumatoid arthritis | Monoarticular juvenile rheumatoid arthritis | Monoarticular juvenile rheumatoid arthritis (disorder)
+BMGC_DS03810,BMG_DS005515,,,,,,,DOID:8398,osteoarthritis,C0157946,,,,,
+BMGC_DS03811,BMG_DS005521,201988000,Transient arthropathy of the shoulder region,,,,,DOID:12084,transient arthropathy,C0158007,,,,,Transient arthropathy of shoulder region | Transient arthropathy of shoulder region (disorder)
+BMGC_DS03812,BMG_DS005524,268062001;287014004;53417006,Articular cartilage disorder,,,,,DOID:6227,articular cartilage disease,C0158073,,,MONDO:0003816,articular cartilage disorder,Articular cartilage disorder | Cartilage disorder | Cartilage disorder (& [articular]) | Cartilage disorder (& [articular]) (disorder) | Articular cartilage disorder | Articular cartilage disorder (disorder) | Articular cartilage disorder | Articular cartilage disease | Articular cartilage disorder (disorder) | Disorder of articular cartilage
+BMGC_DS03813,BMG_DS005529,,,,,,,DOID:528,hydrarthrosis,C0158157,,,,,
+BMGC_DS03814,BMG_DS005532,34671005;95411002,Villonodular synovitis,,,,,DOID:9898,villonodular synovitis,C0158168,,,,,Villonodular synovitis | Villonodular synovitis (disorder)
+BMGC_DS03815,BMG_DS005533,,,,,,,DOID:1166,palindromic rheumatism,C0158178,,,,,
+BMGC_DS03816,BMG_DS005546,202681007;82304009,Kissing spine,,FA72.1,Kissing spine,M48.2,DOID:6643,Baastrup's syndrome,C0158248,,,MONDO:0003956,Baastrup syndrome,Localised idiopathic skeletal hyperostosis (& [kissing spine] or [Baastrup's syndrome]) | Localized idiopathic skeletal hyperostosis (& [kissing spine] or [Baastrup's syndrome]) | Kissing spine | Baastrup's syndrome | Localised idiopathic skeletal hyperostosis (& [kissing spine] or [Baastrup's syndrome]) (disorder) | Kissing spine | Baastrup's syndrome | Overriding of dorsal spinous processes | Osteoarthrosis interspinalis | Localized idiopathic skeletal hyperostosis | Localised idiopathic skeletal hyperostosis | Kissing spine (disorder)
+BMGC_DS03817,BMG_DS005547,36427004,Intervertebral disc disorder,,,,,,,C0158252,,,MONDO:0044339,lumbar disk degenerative disorder,Intervertebral disc disorder | Intervertebral disc disorder (disorder) | Disorder of intervertebral disc
+BMGC_DS03818,BMG_DS005554,,Intervertebral Disc Degeneration,Intervertebral Disc Degeneration,,,,,,C0158266,D055959,603932,MONDO:0011385,intervertebral disk degenerative disorder,
+BMGC_DS03819,BMG_DS005568,202809009,Hypermobility of the coccyx,,,,,DOID:12537,hypermobility of coccyx,C0158295,,,MONDO:0001546,hypermobility of coccyx,Hypermobility of the coccyx | Hypermobility of coccyx | Hypermobility of coccyx (finding)
+BMGC_DS03820,BMG_DS005571,,Adhesive Capsulitis,Bursitis,,,,,,C0158300,D002062,,,,
+BMGC_DS03821,BMG_DS005572,27741009;239957000,Calcific tendinitis of shoulder,,FB40.3,Calcific tendinitis,M75.3,DOID:14181,calcific tendinitis,C0158303,,,,,Calcifying tendinitis of shoulder | Calcific tendinitis of shoulder | Calcifying tendinitis of the shoulder | Calcific tendinitis of shoulder (disorder) | Calcific tendonitis of shoulder | Calcific tendinitis of shoulder | Calcific tendinitis of shoulder (disorder)
+BMGC_DS03822,BMG_DS005573,41137001;202840002,Bicipital tenosynovitis,,,,,DOID:14192,bicipital tenosynovitis,C0158304,,,MONDO:0001905,bicipital tenosynovitis,Bicipital tenosynovitis | Bicipital tenosynovitis (disorder)
+BMGC_DS03823,BMG_DS005577,,,,,,,DOID:12475,pes anserinus tendinitis or bursitis,C0158314,,,,,
+BMGC_DS03824,BMG_DS005578,202869006;44245003,Tibial collateral ligament bursitis,,,,,DOID:13566,tibial collateral ligament bursitis,C0158315,,,MONDO:0001747,tibial collateral ligament bursitis,(Tibial collateral ligament bursitis) or (Pellegrini-Stieda syndrome) | Pellegrini - Stieda syndrome | Tibial collateral ligament bursitis | (Tibial collateral ligament bursitis) or (Pellegrini-Stieda syndrome) (disorder) | Tibial collateral ligament bursitis | Tibial collateral ligament bursitis (disorder)
+BMGC_DS03825,BMG_DS005579,77323000,Inflammation of subtendinous bursa of biceps femoris inferior muscle,,,,,DOID:9358,fibular collateral ligament bursitis,C0158316,,,MONDO:0004764,fibular collateral ligament bursitis,Fibular collateral ligament bursitis | Inflammation of subtendinous bursa of biceps femoris inferior muscle (disorder) | Inflammation of subtendinous bursa of biceps femoris inferior muscle
+BMGC_DS03826,BMG_DS005580,156662006;268089006;37785001,Patellar tendonitis,,,,,DOID:10471,patellar tendinitis,C0158317,,,MONDO:0001042,patellar tendinitis,(Patellar tendinitis) or (Pellegrini-Stieda syndrome) | Patellar tendonitis | Pellegrini-Stieda syndrome | Patellar tendinitis | Pellegrini - Stieda syndrome | (Patellar tendinitis) or (Pellegrini-Stieda syndrome) (disorder) | Pellegrini - Stieda syndrome | Patellar tendonitis | Patellar tendinitis | Pellegrini-Stieda syndrome | (Patellar tendinitis) or (Pellegrini-Stieda syndrome) | (Patellar tendinitis) or (Pellegrini-Stieda syndrome) (disorder) | Patellar tendonitis | Tendinitis of patellar tendon (disorder) | Tendinitis of patellar tendon
+BMGC_DS03827,BMG_DS005582,50127006,Tibialis tendinitis,,,,,DOID:10810,tibialis tendinitis,C0158321,,,MONDO:0001127,tibialis tendinitis,Tibialis tendinitis | Tibialis tendinitis (disorder) | Tibialis tendonitis
+BMGC_DS03828,BMG_DS005583,,Heel Spur,Heel Spur,,,,DOID:210,heel spur,C0158322,D036982,,MONDO:0002209,heel spur,
+BMGC_DS03829,BMG_DS005588,,,,,,,DOID:312,tenosynovitis of foot and ankle,C0158331,,,MONDO:0002517,tenosynovitis of foot and ankle,
+BMGC_DS03830,BMG_DS005589,42812006,Specific bursitis often of occupational origin,,,,,DOID:12223,specific bursitis often of occupational origin,C0158332,,,,,Specific bursitis often of occupational origin | Specific bursitis often of occupational origin (disorder)
+BMGC_DS03831,BMG_DS005591,,,,,,,DOID:9754,ganglion or cyst of synovium/tendon/bursa,C0158336,,,,,
+BMGC_DS03832,BMG_DS005595,,Infectious Myositis,Myositis,,,,,,C0158353,D009220,,MONDO:0023483,infectious myositis,
+BMGC_DS03833,BMG_DS005596,,,,,,,DOID:8936,plantar fascial fibromatosis,C0158360,,,MONDO:0004684,plantar fibromatosis,
+BMGC_DS03834,BMG_DS005597,55925001,Interstitial myositis,,FB3Z,"Disorders of muscles, unspecified",M60.1,DOID:9788,myositis fibrosa,C0158362,,,MONDO:0004881,myositis fibrosa,Interstitial myositis | Myositis fibrosa | Interstitial myositis (disorder)
+BMGC_DS03835,BMG_DS005599,68231009;203146003;156781009;409780002,Acute osteomyelitis,,,,,,,C0158371,,,,,Acute osteomyelitis | Acute bone infection | Bone abscess | Acute osteomyelitis (disorder) | (Bone: [abscess] or [acute infection]) or (acute osteomyelitis) | Bone abscess | Acute bone infection | Acute osteomyelitis | (Bone: [abscess] or [acute infection]) or (acute osteomyelitis) (disorder) | Acute osteomyelitis | Acute osteomyelitis (disorder) | Acute osteomyelitis (disorder) | Acute osteomyelitis
+BMGC_DS03836,BMG_DS005605,62100001,Juvenile osteochondrosis of upper extremity,,,,,DOID:10159,osteonecrosis,C0158442,,,,,Juvenile osteochondrosis of upper extremity | Juvenile osteochondrosis of upper extremity (disorder) | Juvenile osteochondrosis of upper limb
+BMGC_DS03837,BMG_DS005607,32491009,"Juvenile osteochondrosis of foot, NOS",,,,,DOID:11760,Kohler's disease,C0158444,,,MONDO:0016086,osteochondritis of tarsal/metatarsal bone,Juvenile osteochondrosis of foot | Juvenile osteochondrosis of foot (disorder)
+BMGC_DS03838,BMG_DS005608,,Other juvenile osteochondrosis,,,,M92,DOID:8125,osteochondrosis,C0158445,,,,,
+BMGC_DS03839,BMG_DS005609,3345002,Idiopathic osteoporosis,,,,,DOID:12559,idiopathic juvenile osteoporosis,C0158447,,,,,Idiopathic osteoporosis | Idiopathic osteoporosis (disorder)
+BMGC_DS03840,BMG_DS005610,,,,,,,DOID:10159,osteonecrosis,C0158449,,,,,
+BMGC_DS03841,BMG_DS005611,268030004,Osteonecrosis of medial femoral condyle,,,,,DOID:10159,osteonecrosis,C0158450,,,,,Avascular necrosis of medial femoral condyle (disorder) | Avascular necrosis of medial femoral condyle | Osteonecrosis of medial femoral condyle | Aseptic necrosis of medial femoral condyle
+BMGC_DS03842,BMG_DS005612,,,,,,,DOID:10159,osteonecrosis,C0158451,,,,,
+BMGC_DS03843,BMG_DS005622,,,,,,,DOID:2490,congenital nervous system abnormality,C0158538,,,,,
+BMGC_DS03844,BMG_DS005623,,,,,,,,,C0158543,,,MONDO:0022825,congenital cystic eye,
+BMGC_DS03845,BMG_DS005626,,,,,,,,,C0158570,,,MONDO:0024291,vascular malformation,
+BMGC_DS03846,BMG_DS005631,29928006,Congenital insufficiency of mitral valve,,,,,DOID:11502,mitral valve insufficiency,C0158619,,,MONDO:0001298,congenital mitral valve insufficiency,Congenital insufficiency of mitral valve | Congenital mitral insufficiency | Congenital mitral regurgitation | Congenital insufficiency of mitral valve (disorder)
+BMGC_DS03847,BMG_DS005632,,,,,,,DOID:11843,coronary artery anomaly,C0158623,,,MONDO:0001389,congenital coronary artery anomaly,
+BMGC_DS03848,BMG_DS005634,,,,,,,,,C0158646,,,MONDO:0016044,cleft lip/palate,
+BMGC_DS03849,BMG_DS005635,,,,,,,DOID:9296,cleft lip,C0158651,,,,,
+BMGC_DS03850,BMG_DS005636,,,,,,,DOID:0111549,aplasia of lacrimal and salivary glands,C0158667,,180920,MONDO:0008397,aplasia of lacrimal and salivary glands,
+BMGC_DS03851,BMG_DS005637,,,,,,,DOID:12641,displacement of cardia through esophageal hiatus,C0158674,,,MONDO:0001562,displacement of cardia through esophageal hiatus,
+BMGC_DS03852,BMG_DS005638,72925005,Polycystic liver disease,,,,,DOID:0050770,polycystic liver disease,C0158683,C536330,MTHU014343,MONDO:0000447,autosomal dominant polycystic liver disease,Congenital cystic disease of liver | Congenital polycystic disease of liver | Fibrocystic disease of liver | Congenital hepatic cyst | PLD - Polycystic liver disease | Congenital polycystic liver disease | Fibrocystic liver disease | Polycystic liver disease | Cystic disease of liver | Congenital cystic disease of liver (disorder) | Congenital cystic liver
+BMGC_DS03853,BMG_DS005639,,,,,,,DOID:9827,radioulnar synostosis,C0158761,,,MONDO:0017985,congenital radioulnar synostosis,
+BMGC_DS03854,BMG_DS005641,,,,,,,,,C0158779,,117900,MONDO:0007303,cervical rib disease,
+BMGC_DS03855,BMG_DS005643,,Fetal Malnutrition,Fetal Nutrition Disorders,,,,,,C0158850,D048070,,,,
+BMGC_DS03856,BMG_DS005652,,Congenital Cytomegalovirus Infection,Cytomegalovirus Infections,,,,,,C0158945,D003586,,,,
+BMGC_DS03857,BMG_DS005653,42052009;206340009,Omphalitis of the newborn,,,,,,,C0158947,,,,,Umbilical infection of newborn | Infection of navel cord | Omphalitis of newborn (disorder) | Omphalitis of newborn | Umbilical stump infection of newborn | Umbilical stump infection of the newborn (& [omphalitis]) | Omphalitis of the newborn | Umbilical stump infection of the newborn | Umbilical stump infection of the newborn (& [omphalitis]) (disorder)
+BMGC_DS03858,BMG_DS005654,3468005,Neonatal infective mastitis,,KA65.3,Neonatal infectious mastitis,P39.0,DOID:13520,neonatal infective mastitis,C0158948,,,MONDO:0001736,neonatal infective mastitis,Neonatal infective mastitis | Neonatal infective mastitis (disorder)
+BMGC_DS03859,BMG_DS005655,86986002,Hemolytic disease of fetus OR newborn due to RhD isoimmunization,,,,,,,C0158962,,,,,Rh hemolytic disease of the newborn | Rh isoimmunization of the newborn | Anemia due to Rh isoimmunization | Hemolytic disease due to Rh isoimmunization | Rhesus isoimmunization of the newborn | Erythroblastosis fetalis due to Rh isoimmunization | Jaundice due to Rh isoimmunization of the newborn | Hemolytic disease of fetus OR newborn due to Rh isoimmunization | Hemolytic disease - Rh | Hemolytic disease due to rhesus isoimmunization | Rh HDN - Rh hemolytic disease of the newborn | Rh isoimmunisation of the newborn | Haemolytic disease of fetus OR newborn due to Rh isoimmunisation | Haemolytic disease due to rhesus isoimmunisation | Rh haemolytic disease of the newborn | Rh HDN - Rh haemolytic disease of the newborn | Haemolytic disease - Rh | Rhesus isoimmunisation of the newborn | Erythroblastosis fetalis due to Rh isoimmunisation | Haemolytic disease due to Rh isoimmunisation | Jaundice due to Rh isoimmunisation of the newborn | Anaemia due to Rh isoimmunisation | Hemolytic disease of fetus OR newborn due to RhD isoimmunization (disorder) | Haemolytic disease of fetus OR newborn due to RhD isoimmunisation | Hemolytic disease of fetus OR newborn due to RhD isoimmunization | Haemolytic disease of foetus OR newborn due to RhD isoimmunisation | Haemolytic disease of foetus OR newborn due to Rh isoimmunisation | Erythroblastosis foetalis due to Rh isoimmunisation
+BMGC_DS03860,BMG_DS005657,10877007;206463003,Perinatal jaundice due to hepatocellular damage,,,,,DOID:11452,perinatal jaundice due to hepatocellular damage,C0158976,,,MONDO:0006595,perinatal jaundice due to hepatocellular damage,Perinatal jaundice due to hepatocellular damage | Perinatal jaundice due to hepatocellular damage (finding)
+BMGC_DS03861,BMG_DS005658,49817004,Neonatal diabetes mellitus,,KB60.2Z,"Neonatal diabetes mellitus, unspecified",P70.2,DOID:11717;DOID:0060334,neonatal diabetes | transient neonatal diabetes mellitus,C0158981,,MTHU046151,MONDO:0016391,neonatal diabetes mellitus,Neonatal diabetes mellitus | Neonatal diabetes mellitus (disorder)
+BMGC_DS03862,BMG_DS005659,,Neonatal Myasthenia Gravis,"Myasthenia Gravis, Neonatal",,,,DOID:14043,neonatal myasthenia gravis,C0158982,D020941,,MONDO:0006866,neonatal myasthenia gravis,
+BMGC_DS03863,BMG_DS005660,13795004,Neonatal thyrotoxicosis,,KB62.0,Transitory neonatal hyperthyroidism,P72.1,DOID:12573,neonatal thyrotoxicosis,C0158983,,,MONDO:0001555,neonatal thyrotoxicosis,Neonatal thyrotoxicosis | Neonatal thyrotoxicosis (disorder)
+BMGC_DS03864,BMG_DS005662,52767006;157147000,Neonatal hypoglycemia,,,,,,,C0158986,,MTHU037871,,,Neonatal hypoglycemia | Neonatal hypoglycaemia | Neonatal hypoglycemia (disorder) | Neonatal hypoglycaemia | Neonatal hypoglycemia | Neonatal hypoglycaemia (disorder)
+BMGC_DS03865,BMG_DS005664,,,,,,,DOID:9771,transient neonatal thrombocytopenia,C0158991,,,MONDO:0004877,transient neonatal thrombocytopenia,
+BMGC_DS03866,BMG_DS005665,34417008,Disseminated intravascular coagulation in newborn,,,,,DOID:11246,DIC in newborn,C0158992,,,MONDO:0001242,disseminated intravascular coagulation in newborn,Disseminated intravascular coagulation in newborn | DIC in newborn | Disseminated intravascular coagulation in newborn (disorder) | Newborn defibrination syndrome | Newborn disseminated intravascular coagulation
+BMGC_DS03867,BMG_DS005668,47100003,Anemia of prematurity,,KA8B,Anaemia of prematurity,P61.2,DOID:11243,anemia of prematurity,C0158996,,,MONDO:0001239,anemia of prematurity,Anemia of prematurity | Anaemia of prematurity | Anemia of prematurity (disorder)
+BMGC_DS03868,BMG_DS005669,55444004,Transient neonatal neutropenia (disorder),,,,,DOID:11245,transient neonatal neutropenia,C0158997,,,MONDO:0001241,transient neonatal neutropenia,Transient neonatal neutropenia | Transient neonatal neutropenia (disorder)
+BMGC_DS03869,BMG_DS005671,65390006;206526009,Perinatal intestinal perforation,,KB86.Z,"Postnatal intestinal perforation, unspecified",P78.0,DOID:2073,perinatal intestinal perforation,C0159006,,,MONDO:0002196,perinatal intestinal perforation,Perinatal intestinal perforation | Perinatal intestinal perforation (disorder) | Perinatal intestinal perforation | Perinatal intestinal perforation (finding)
+BMGC_DS03870,BMG_DS005675,87476004,Convulsions in the newborn,,,,,,,C0159020,,,,,Neonatal seizure (finding) | Neonatal seizure
+BMGC_DS03871,BMG_DS005688,62660000,Conjunctival deposit,,,,,DOID:11653,conjunctival deposit,C0162280,,,MONDO:0001331,conjunctival deposit,Conjunctival deposit | Conjunctival deposit (disorder) | Conjunctival deposits
+BMGC_DS03872,BMG_DS005689,74460005,Corneal deposit,,,,,DOID:11547,corneal deposit,C0162281,,,MONDO:0001308,corneal deposit,Corneal deposit | Corneal deposit (disorder)
+BMGC_DS03873,BMG_DS005690,,Nephrogenic Diabetes Insipidus,"Diabetes Insipidus, Nephrogenic",,,,DOID:12387,nephrogenic diabetes insipidus,C0162283,D018500,,MONDO:0016383,nephrogenic diabetes insipidus,
+BMGC_DS03874,BMG_DS005691,,,,,,,DOID:12510,retinal ischemia,C0162291,,,MONDO:0001538,retinal ischemia,
+BMGC_DS03875,BMG_DS005692,,External Ophthalmoplegia,Ophthalmoplegia,,,,,,C0162292,D009886,,,,
+BMGC_DS03876,BMG_DS005693,268070006;35678005;156616003,Polyarthralgia,Arthralgia,,,,,,C0162296,D018771,,,,(Joint: [disorder NOS] or [unstable]) or (polyarthralgia) | Unstable joint | Polyarthralgia | Joint disorder NOS | Joint unstable | (Joint: [disorder NOS] or [unstable]) or (polyarthralgia) (disorder) | Polyarthralgia | Multiple joint pain | Arthralgia of multiple joints | Pain of multiple joints | Pain of multiple joints (finding) | (Joint: [disorder NOS] or [unstable]) or (polyarthralgia) | Unstable joint | Polyarthralgia | Joint disorder NOS | Joint unstable | (Joint: [disorder NOS] or [unstable]) or (polyarthralgia) (finding)
+BMGC_DS03877,BMG_DS005694,20342001,Calculus in urethra,,GB71.1,Calculus in urethra,N21.1,DOID:9589,urethral calculus,C0162301,,,MONDO:0004826,urethral calculus,Calculus in urethra | Urethral stone | Urethral calculus | Calculus in urethra (disorder)
+BMGC_DS03878,BMG_DS005695,65389002,Adrenoleukodystrophy,Adrenoleukodystrophy,,,,DOID:10588,adrenoleukodystrophy,C0162309,D000326,300100,MONDO:0018544,adrenoleukodystrophy,Adrenoleukodystrophy | Bronze Schilder disease | Schilder-Addison complex | Siemerling-Creutzfeldt disease | Adrenoleukodystrophy (disorder) | X-linked adrenoleucodystrophy | Adrenoleucodystrophy | ALD - adrenoleukodystrophy | X-linked adrenoleukodystrophy
+BMGC_DS03879,BMG_DS005696,,Androgenetic Alopecia,Alopecia,,,,,,C0162311,D000505,,MONDO:0005339,androgenetic alopecia,
+BMGC_DS03880,BMG_DS005697,154787005;87522002;267553005,Iron deficiency anemia,,,,D50,,,C0162316,,MTHU036458,MONDO:0001356,iron deficiency anemia,(Anaemia: [iron deficiency] or [microcytic]) or (Kelly-Paterson syndrome) or (Plummer-Vinson syndrome) | (Anemia: [iron deficiency] or [microcytic]) or (Kelly-Paterson syndrome) or (Plummer-Vinson syndrome) | Kelly-Paterson syndrome | Plummer-Vinson syndrome | Plummer-Vinson syndr. | Kelly-Paterson synd. | Anemia - iron defic. | Microcytic anemia | Iron deficiency anemias | Iron deficiency anemia | Microcytic anaemia | Iron deficiency anaemias | Anaemia - iron defic. | Iron deficiency anaemia | (Anaemia: [iron deficiency] or [microcytic]) or (Kelly-Paterson syndrome) or (Plummer-Vinson syndrome) (disorder) | Iron deficiency anemia | Asiderotic anemia | Chlorotic anemia | Sideropenic anemia | Iron deficiency anaemia | IDA - Iron deficiency anemia | Iron deficiency anemia syndrome | Asiderotic anaemia | IDA - Iron deficiency anaemia | Sideropenic anaemia | Iron deficiency anaemia syndrome | Chlorotic anaemia | Iron deficiency anemia (disorder) | (Anaemia: [iron deficiency] or [microcytic]) or (Kelly-Paterson syndrome) or (Plummer-Vinson syndrome) | Anemia - iron defic. | Iron deficiency anemia | Iron deficiency anemias | Microcytic anemia | Kelly-Paterson syndrome | Plummer-Vinson syndrome | Plummer-Vinson syndr. | Kelly-Paterson synd. | Iron deficiency anaemias | Iron deficiency anaemia | Microcytic anaemia | Anaemia - iron defic. | (Anemia: [iron deficiency] or [microcytic]) or (Kelly-Paterson syndrome) or (Plummer-Vinson syndrome) | (Anaemia: [iron deficiency] or [microcytic]) or (Kelly-Paterson syndrome) or (Plummer-Vinson syndrome) (disorder)
+BMGC_DS03881,BMG_DS005698,202032009;41397009;30701005;416956002,Polyarthritis,Arthritis,,,,,,C0162323,D001168,MTHU041499,MONDO:0024280,polyarticular arthritis,Unspecified polyarthropathy or polyarthritis NOS | Polyarthritis | (Unspecified polyarthropathy or polyarthritis NOS) or (polyarthritis) | (Unspecified polyarthropathy or polyarthritis NOS) or (polyarthritis) (disorder) | Polyarthritis | Polyarthritis (disorder) | Inflammatory polyarthropathy | Inflammatory polyarthritis | Polyarthritis | Undifferentiated inflammatory polyarthritis | Inflammatory polyarthropathy (disorder) | Undifferentiated inflammatory polyarthritis (disorder) | Undifferentiated inflammatory polyarthritis | Polyarthritis
+BMGC_DS03882,BMG_DS005699,4826006;239007005,Christ-Siemens-Touraine syndrome,,,,,DOID:0111664;DOID:14793,hypohidrotic ectodermal dysplasia | ectodermal dysplasia 1,C0162359,,305100,MONDO:0010585,X-linked hypohidrotic ectodermal dysplasia,Hypohidrotic ectodermal dysplasia syndrome | Hypohidrotic ectodermal dysplasia syndrome (disorder) | Christ-Siemens-Touraine syndrome | CST - Christ-Siemens-Touraine syndrome | Hypohidrotic X-linked ectodermal dysplasia | Hypohidrotic X-linked ectodermal dysplasia (disorder)
+BMGC_DS03883,BMG_DS005700,,Hidrotic Ectodermal Dysplasia,Ectodermal Dysplasia,,,,DOID:14693,Clouston syndrome,C0162361,D004476,129500,MONDO:0007510,Clouston syndrome,
+BMGC_DS03884,BMG_DS005701,,"Granuloma, Giant Cell Reparative","Granuloma, Giant Cell",,,,DOID:1866,giant cell reparative granuloma,C0162375,D006101,,MONDO:0006770,giant cell reparative granuloma,
+BMGC_DS03885,BMG_DS005702,,Miliaria Rubra,Miliaria,,,,DOID:11153,miliaria rubra,C0162423,D008883,,MONDO:0006581,miliaria rubra,
+BMGC_DS03886,BMG_DS005703,2492009,Malnutrition,Malnutrition,,,,,,C0162429,D044342,MTHU026060,,,Nutritional disorder | Nutritional disease | Disorder of nutrition | Malnutrition | Nutritional disorder (disorder)
+BMGC_DS03887,BMG_DS005704,,Parapsoriasis en Plaques,Parapsoriasis,,,,,,C0162442,D010267,,,,
+BMGC_DS03888,BMG_DS005707,,,,,,,DOID:997,uterine inversion,C0162482,,,MONDO:0004936,uterine inversion,
+BMGC_DS03889,BMG_DS005712,,Caroli Disease,Caroli Disease,,,,DOID:0050876,Caroli disease,C0162510,D016767,600643,MONDO:0010913,Caroli disease,
+BMGC_DS03890,BMG_DS005713,,AIDS-Related Opportunistic Infections,AIDS-Related Opportunistic Infections,,,,,,C0162526,D017088,,,,
+BMGC_DS03891,BMG_DS005714,,"Colitis, Ischemic","Colitis, Ischemic",,,,DOID:0060181,ischemic colitis,C0162529,D017091,,MONDO:0000701,ischemic colitis,
+BMGC_DS03892,BMG_DS005715,,,,,,,DOID:13271,cutaneous porphyria,C0162530,,,,,
+BMGC_DS03893,BMG_DS005716,,Hereditary Coproporphyria,"Coproporphyria, Hereditary",,,,DOID:13269,hereditary coproporphyria,C0162531,D046349,121300,MONDO:0007369,hereditary coproporphyria,
+BMGC_DS03894,BMG_DS005717,,Variegate Porphyria,"Porphyria, Variegate",,,,DOID:4346,variegate porphyria,C0162532,D046350,176200,MONDO:0008297,variegate porphyria,
+BMGC_DS03895,BMG_DS005718,,"Porphyrias, Hepatic","Porphyrias, Hepatic",,,,DOID:3133,acute porphyria,C0162533,D017094,,MONDO:0002520,hepatic porphyria,
+BMGC_DS03896,BMG_DS005719,,Prion Diseases,Prion Diseases,,,,DOID:649,prion disease,C0162534,D017096,,MONDO:0005429,prion disease,
+BMGC_DS03897,BMG_DS005720,29260007,Immunoglobulin A deficiency (disorder),,,,,DOID:0060025;DOID:11701,immunoglobulin alpha deficiency | selective IgA deficiency disease,C0162538,,,,,Immunoglobulin A deficiency | IgA deficiency | Immunoglobulin A deficiency (disorder)
+BMGC_DS03898,BMG_DS005721,12631000119106,Immunoglobulin G deficiency (disorder),,,,,DOID:14176,selective IgG deficiency disease,C0162539,,,MONDO:0001901,selective IgG subclass deficiency,Immunoglobulin G deficiency (disorder) | Immunoglobulin G deficiency
+BMGC_DS03899,BMG_DS005722,,"Akathisia, Tardive","Akathisia, Drug-Induced",,,,,,C0162549,D017109,,,,
+BMGC_DS03900,BMG_DS005723,,"Akathisia, Drug-Induced","Akathisia, Drug-Induced",,,,,,C0162550,D017109,,MONDO:0006731,drug-induced akathisia,
+BMGC_DS03901,BMG_DS005724,,"Liver Failure, Acute","Liver Failure, Acute",,,,,,C0162557,D017114,,MONDO:0019542,acute liver failure,
+BMGC_DS03902,BMG_DS005725,90842001;190914003;234422006,Acute intermittent porphyria,,,,,DOID:3890,acute intermittent porphyria,C0162565,,176000,MONDO:0008294,acute intermittent porphyria,Acute intermittent porphyria | Acute intermittent porphyria (disorder) | Acute intermittent porphyria | AIP - Acute intermittent porphyria | Acute intermittent porphyria (disorder) | Acute intermittent porphyria | AIP - Acute intermittent porphyria | Pyrroloporphyria | Acute porphyria | Intermittent acute porphyria | Swedish porphyria | Intermittent acute porphyria syndrome | Acute intermittent porphyria (disorder)
+BMGC_DS03903,BMG_DS005726,,Porphyria Cutanea Tarda,Porphyria Cutanea Tarda,,,,DOID:3132,porphyria cutanea tarda,C0162566,D017119,,MONDO:0015104,porphyria cutanea tarda,
+BMGC_DS03904,BMG_DS005727,,Erythropoietic Protoporphyria,"Protoporphyria, Erythropoietic",,,,DOID:13270,erythropoietic protoporphyria,C0162568,D046351,,MONDO:0001676,erythropoietic protoporphyria,
+BMGC_DS03905,BMG_DS005728,,Hepatoerythropoietic Porphyria,"Porphyria, Hepatoerythropoietic",,,,DOID:5230,hepatoerythropoietic porphyria,C0162569,D017121,,MONDO:0019799,hepatoerythropoietic porphyria,
+BMGC_DS03906,BMG_DS005729,442652006;187173002;32183007,Anisakiasis,Anisakiasis,1F61,Anisakiasis,B81.0,DOID:7033,anisakiasis,C0162576,D017129,,MONDO:0015200,anisakiasis,Anisakiasis | Infection by Anisakis larva | Infection caused by Anisakis larva | Infection caused by Anisakis larva (disorder) | Infection by Anisakis larva | Anisakiosis | Herring worm disease | Herringworm disease | Anisakiasis | Anisakiasis (disorder) | Infection by Anisakis larva | Infection by Anisakis larva (disorder)
+BMGC_DS03907,BMG_DS005734,,"Skin Diseases, Bacterial","Skin Diseases, Bacterial",,,,,,C0162627,D017192,,MONDO:0024295,skin disease caused by bacterial infection,
+BMGC_DS03908,BMG_DS005735,,"Skin Diseases, Viral","Skin Diseases, Viral",,,,,,C0162628,D017193,,,,
+BMGC_DS03909,BMG_DS005736,,Oxyurida Infections,Oxyurida Infections,,,,,,C0162629,D017194,,,,
+BMGC_DS03910,BMG_DS005738,,Angelman Syndrome,Angelman Syndrome,,,,DOID:1932,Angelman syndrome,C0162635,D017204,105830,MONDO:0007113,Angelman syndrome,
+BMGC_DS03911,BMG_DS005741,,Root Caries,Root Caries,,,,DOID:14089,root caries,C0162644,D017213,,MONDO:0006957,root caries,
+BMGC_DS03912,BMG_DS005742,196759006,Gastric outlet obstruction,,,,,DOID:3122,gastric outlet obstruction,C0162651,,,,,(Adult hypertrophic pyloric stenosis) or (gastric outlet obstruction) | Gastric outlet obstruction | Gastric outflow obstruction | Adult hypertrophic pyloric stenosis | (Adult hypertrophic pyloric stenosis) or (gastric outlet obstruction) (disorder)
+BMGC_DS03913,BMG_DS005743,,Mitochondrial Encephalomyopathies,Mitochondrial Encephalomyopathies,,,,DOID:890,mitochondrial encephalomyopathy,C0162666,D017237,,MONDO:0004675,mitochondrial encephalomyopathy,
+BMGC_DS03914,BMG_DS005744,,Megaconial Myopathies,Mitochondrial Myopathies,,,,,,C0162668,D017240,,,,
+BMGC_DS03915,BMG_DS005745,,Pleoconial Myopathies,Mitochondrial Myopathies,,,,,,C0162669,D017240,,,,
+BMGC_DS03916,BMG_DS005746,,Mitochondrial Myopathies,Mitochondrial Myopathies,,,,DOID:699,mitochondrial myopathy,C0162670,D017240,,MONDO:0009637,inborn mitochondrial myopathy,
+BMGC_DS03917,BMG_DS005747,,MELAS Syndrome,MELAS Syndrome,,,,DOID:3687,MELAS syndrome,C0162671,D017241,540000,MONDO:0010789,MELAS syndrome,
+BMGC_DS03918,BMG_DS005748,,MERRF Syndrome,MERRF Syndrome,,,,DOID:310,MERRF syndrome,C0162672,D017243,545000,MONDO:0010790,MERRF syndrome,
+BMGC_DS03919,BMG_DS005749,194126004;46252003;194034008,Chronic progressive external ophthalmoplegia,,,,,DOID:12558,chronic progressive external ophthalmoplegia,C0162674,,,MONDO:0005181,progressive external ophthalmoplegia,Chronic progressive external ophthalmoplegia | Chronic progressive external ophthalmoplegia (disorder) | Progressive external ophthalmoplegia | Graefe's disease | Chronic progressive ophthalmoplegia | Chronic progressive external ophthalmoplegia | CPEO - chronic progressive external ophthalmoplegia | Progressive external ophthalmoplegia (disorder) | PEO - Progressive external ophthalmoplegia
+BMGC_DS03920,BMG_DS005750,,Caliciviridae Infections,Caliciviridae Infections,,,,,,C0162677,D017250,,MONDO:0005687,Caliciviridae infectious disease,
+BMGC_DS03921,BMG_DS005751,,,,,,,DOID:8712,neurofibromatosis,C0162678,,,MONDO:0021061,neurofibromatosis,
+BMGC_DS03922,BMG_DS005752,,Tick-Borne Infections,Tick-Borne Diseases,,,,,,C0162699,D017282,,,,
+BMGC_DS03923,BMG_DS005753,,Tick-Borne Diseases,Tick-Borne Diseases,,,,,,C0162700,D017282,,MONDO:0025294,tick-borne infectious disease,
+BMGC_DS03924,BMG_DS005754,,HELLP Syndrome,HELLP Syndrome,,,,DOID:13133,HELLP syndrome,C0162739,D017359,,MONDO:0008585,HELLP syndrome,
+BMGC_DS03925,BMG_DS005755,,Right Ventricular Hypertrophy,"Hypertrophy, Right Ventricular",,,,,,C0162770,D017380,,,,
+BMGC_DS03926,BMG_DS005756,,Kallmann Syndrome,Kallmann Syndrome,,,,DOID:3614,Kallmann syndrome,C0162809,D017436,,MONDO:0018800,Kallmann syndrome,
+BMGC_DS03927,BMG_DS005759,,"Skin Diseases, Vascular","Skin Diseases, Vascular",,,,DOID:9540,vascular skin disease,C0162819,D017445,,MONDO:0019293,skin vascular disease,
+BMGC_DS03928,BMG_DS005760,,"Dermatitis, Allergic Contact","Dermatitis, Allergic Contact",,,,DOID:3042,allergic contact dermatitis,C0162820,D017449,,MONDO:0006525,allergic contact dermatitis,
+BMGC_DS03929,BMG_DS005761,,"Dermatitis, Irritant","Dermatitis, Irritant",,,,DOID:2772,irritant dermatitis,C0162823,D017453,,MONDO:0006564,irritant dermatitis,
+BMGC_DS03930,BMG_DS005762,,"Dermatitis, Photoallergic","Dermatitis, Photoallergic",,,,DOID:3818,photoallergic dermatitis,C0162824,D017454,,MONDO:0006596,photoallergic dermatitis,
+BMGC_DS03931,BMG_DS005763,,"Dermatitis, Phototoxic","Dermatitis, Phototoxic",,,,DOID:4407,phototoxic dermatitis,C0162830,D017484,,MONDO:0006598,phototoxic dermatitis,
+BMGC_DS03932,BMG_DS005764,,,,,,,,,C0162834,,,MONDO:0019289,hyperpigmentation of the skin,
+BMGC_DS03933,BMG_DS005765,201284005,Hypopigmentation disorder,,,,,,,C0162835,,,MONDO:0019290,hypopigmentation of the skin,Hypopigmentation disorder | Hypopigmentation disorder (disorder)
+BMGC_DS03934,BMG_DS005766,,Hidradenitis Suppurativa,Hidradenitis Suppurativa,,,,DOID:2280,hidradenitis suppurativa,C0162836,D017497,,MONDO:0006559,hidradenitis suppurativa,
+BMGC_DS03935,BMG_DS005767,,"Porokeratosis, Palmoplantar",Porokeratosis,,,,,,C0162838,D017499,175850,MONDO:0008291,porokeratosis plantaris palmaris et disseminata,
+BMGC_DS03936,BMG_DS005768,,,,,,,DOID:3805,porokeratosis,C0162839,,,MONDO:0006602,porokeratosis,
+BMGC_DS03937,BMG_DS005769,,Lichenoid Eruptions,Lichenoid Eruptions,,,,,,C0162848,D017512,,,,
+BMGC_DS03938,BMG_DS005770,,Lichen Nitidus,Lichen Nitidus,,,,DOID:8573,lichen nitidus,C0162849,D017513,,MONDO:0006571,lichen nitidus,
+BMGC_DS03939,BMG_DS005775,,Mucinoses,Mucinoses,,,,DOID:3141,mucinoses,C0162855,D017520,,MONDO:0002523,cutaneous mucinosis,
+BMGC_DS03940,BMG_DS005776,,"Aneurysm, Ruptured","Aneurysm, Ruptured",,,,,,C0162869,D017542,,,,
+BMGC_DS03941,BMG_DS005777,,,,,,,DOID:7693,abdominal aortic aneurysm,C0162871,,,MONDO:0005350,abdominal aortic aneurysm,
+BMGC_DS03942,BMG_DS005778,,,,,,,DOID:14004,thoracic aortic aneurysm,C0162872,,,MONDO:0005396,thoracic aortic aneurysm,
+BMGC_DS03943,BMG_DS005780,15489004;398680004,Citrullinemia,Citrullinemia,,,E72.23,DOID:9273,citrullinemia,C0175683,D020159,MTHU038623,MONDO:0015991,citrullinemia,Citrullinemia | Arginosuccinate synthetase deficiency | Argininosuccinate synthase deficiency | Argininosuccinase deficiency | ASAS deficiency | ASA synthase deficiency | ASS deficiency | Citrullinuria | Citrullinaemia | Citrullinemia (disorder) | Citrullinemia (disorder) | Citrullinaemia | Citrullinemia
+BMGC_DS03944,BMG_DS005781,2593002,Dubowitz syndrome,,,,Q87.19,DOID:14796,Dubowitz syndrome,C0175691,C535718,223370,MONDO:0009124,Dubowitz syndrome,Dubowitz's syndrome | Dubowitz's syndrome (disorder) | Dubowitz syndrome
+BMGC_DS03945,BMG_DS005782,75979009,Johanson-Blizzard syndrome,,,,,DOID:14694,Johanson-Blizzard syndrome,C0175692,,260450;243800,MONDO:0009479,Johanson-Blizzard syndrome,Johanson-Blizzard syndrome | Johanson-Blizzard syndrome (disorder)
+BMGC_DS03946,BMG_DS005783,15069006,Russell-Silver syndrome,,,,Q87.19,DOID:14681,Silver-Russell syndrome,C0175693,,,MONDO:0008394,Silver-Russell syndrome,Russell-Silver syndrome | Silver syndrome | Russell's syndrome | Russell-Silver syndrome (disorder)
+BMGC_DS03947,BMG_DS005784,,Smith-Lemli-Opitz Syndrome,Smith-Lemli-Opitz Syndrome,,,,DOID:14692,Smith-Lemli-Opitz syndrome,C0175694,D019082,270400,MONDO:0010035,Smith-Lemli-Opitz syndrome,
+BMGC_DS03948,BMG_DS005785,75968004,Sotos' syndrome,,,,,DOID:14748,Sotos syndrome,C0175695,,117550,MONDO:0019349,Sotos syndrome,Sotos' syndrome | Cerebral gigantism syndrome | Cerebral giant | Sotos' syndrome (disorder) | Cerebral gigantism | Sotos syndrome
+BMGC_DS03949,BMG_DS005787,79261008,Van der Woude syndrome,,,,,DOID:0060239,Van der Woude syndrome,C0175697,C536528,,MONDO:0019508,van der Woude syndrome,Van der Woude syndrome | Lip-pit-cleft lip syndrome | Van der Woude syndrome (disorder)
+BMGC_DS03950,BMG_DS005788,,Saethre-Chotzen Syndrome,Acrocephalosyndactylia,,,,DOID:14768,Saethre-Chotzen syndrome,C0175699,D000168,101400,MONDO:0007042,Saethre-Chotzen syndrome,
+BMGC_DS03951,BMG_DS005789,62628008,Multiple synostosis syndrome,,,,,DOID:14762,calcaneonavicular coalition,C0175700,,,MONDO:0017923,multiple synostoses syndrome,Multiple synostosis syndrome | Symphalangism syndrome | Multiple synostosis syndrome (disorder)
+BMGC_DS03952,BMG_DS005790,205809002;14921002,Aarskog syndrome,,,,Q87.19,DOID:6683,X-linked Aarskog syndrome,C0175701,,305400,MONDO:0010589,"Aarskog-Scott syndrome, X-linked",Aarskog syndrome | Aarskog syndrome (disorder)
+BMGC_DS03953,BMG_DS005791,,Williams Syndrome,Williams Syndrome,,,,DOID:1928,Williams-Beuren syndrome,C0175702,D018980,194050,MONDO:0008678,Williams syndrome,
+BMGC_DS03954,BMG_DS005792,,Thrombocytopenia-Absent Radius Syndrome,,,,,DOID:14699,thrombocytopenia-absent radius syndrome,C0175703,C536940,274000,MONDO:0010121,thrombocytopenia-absent radius syndrome,
+BMGC_DS03955,BMG_DS005793,,LEOPARD Syndrome,LEOPARD Syndrome,,,,DOID:14291,Noonan syndrome with multiple lentigines,C0175704,D044542,,MONDO:0007893,Noonan syndrome with multiple lentigines,
+BMGC_DS03956,BMG_DS005794,,Asplenia Syndrome,Heterotaxy Syndrome,,,,,,C0175707,D059446,,,,
+BMGC_DS03957,BMG_DS005796,82077006;193223007,Centronuclear myopathy,,,,G71.22,DOID:14717,centronuclear myopathy,C0175709,,,MONDO:0018947,centronuclear myopathy,Myotubular myopathy | Centronuclear myopathy | Myotubular myopathy (disorder) | Centronuclear myopathy | Centronuclear myopathy (disorder)
+BMGC_DS03958,BMG_DS005797,80651009,Aicardi's syndrome,,,,,DOID:8461,Aicardi syndrome,C0175713,,304050,MONDO:0010568,Aicardi syndrome,Aicardi's syndrome | Aicardi's syndrome (disorder) | AIC - Aicardi syndrome | Aicardi syndrome
+BMGC_DS03959,BMG_DS005798,,,,,,,,,C0175754,,217990,MONDO:0009022,"corpus callosum, agenesis of",
+BMGC_DS03960,BMG_DS005800,268343006;63387002;156993005,Larsen syndrome,,,,,,,C0175778,,150250,MONDO:0007875,Larsen syndrome,(Congenital limb deformity NOS) or (pes cavus) or (claw toe) or (dysmorphic toes) or (Larsen's syndrome) | Pes cavus | Dysmorphic toes | Congenital limb deformity NOS | Claw toe | Larsen syndrome | Cavus - pes | Larsen's syndrome | (Congenital limb deformity NOS) or (pes cavus) or (claw toe) or (dysmorphic toes) or (Larsen's syndrome) (disorder) | Larsen syndrome | Larsen syndrome (disorder) | (Congenital limb deformity NOS) or (pes cavus) or (claw toe) or (dysmorphic toes) or (Larsen's syndrome) | Cavus - pes | Congenital limb deformity NOS | Larsen's syndrome | Pes cavus | Claw toe | Dysmorphic toes | Larsen syndrome | (Congenital limb deformity NOS) or (pes cavus) or (claw toe) or (dysmorphic toes) or (Larsen's syndrome) (disorder)
+BMGC_DS03961,BMG_DS005801,,,,,,,,,C0175816,,,MONDO:0016450,"autoimmune hemolytic anemia, cold type",
+BMGC_DS03962,BMG_DS005803,266368002,Post-inflammatory pulmonary fibrosis,,,,,DOID:12123,postinflammatory pulmonary fibrosis,C0175999,,,MONDO:0001438,postinflammatory pulmonary fibrosis,Post-inflammatory pulmonary fibrosis | Post-inflammatory pulmonary fibrosis (disorder) | Postinflammatory pulmonary fibrosis
+BMGC_DS03963,BMG_DS005804,266071000;187266003,Intestinal infectious disease (disorder),,,,,DOID:100,intestinal infectious disease,C0178238,,,MONDO:0000916,intestinal infectious disease,Intestinal infectious disease | Intestinal infection | Infectious disease of intestine | Intestinal infectious disease (disorder) | Intestinal infectious disease | Intestinal infectious disease (disorder)
+BMGC_DS03964,BMG_DS005809,,Other disorders of central nervous system,,,,G96,,,C0178266,,,,,
+BMGC_DS03965,BMG_DS005819,41614006,Hypoplastic anemia,,,,,,,C0178416,,MTHU014878,,,Hypoplastic anemia | Hypoplastic anaemia | Hypoplastic anemia (disorder)
+BMGC_DS03966,BMG_DS005820,,,,,,,DOID:1618,breast fibroadenoma,C0178421,,,MONDO:0002056,breast fibroadenoma,
+BMGC_DS03967,BMG_DS005821,41962002,Oligohydramnios sequence,,,,,DOID:12594,Potter's syndrome,C0178426,,,MONDO:0001558,Potter sequence,Oligohydramnios sequence | Potter syndrome | Renofacial syndrome | Renal agenesis syndrome | Congenital absence of kidneys syndrome | Oligohydramnios sequence (disorder) | BRA - Bilateral renal agenesis | Potter's anomaly of the kidney | Bilateral congenital absence of kidneys
+BMGC_DS03968,BMG_DS005823,,Cerebral Hypoxia-Ischemia,"Hypoxia-Ischemia, Brain",,,,,,C0178540,D020925,,,,
+BMGC_DS03969,BMG_DS005825,197661001,Glomerulosclerosis (disorder),,,,,,,C0178664,,,MONDO:0000490,glomerulosclerosis,Glomerulosclerosis | Glomerulosclerosis (disorder)
+BMGC_DS03970,BMG_DS005829,,,,,,,DOID:193,reproductive organ cancer,C0178830,,,MONDO:0006054,reproductive system neoplasm,
+BMGC_DS03971,BMG_DS005830,7163005,Urinary tract obstruction,,,,,DOID:5200,urinary tract obstruction,C0178879,,,MONDO:0003330,urinary tract obstruction,Urinary tract obstruction | Obstructive uropathy | Urinary tract obstruction (disorder)
+BMGC_DS03972,BMG_DS005832,,,,,,,DOID:5675,cribriform carcinoma,C0205643,,,MONDO:0006176,cribriform carcinoma,
+BMGC_DS03973,BMG_DS005833,,,,,,,DOID:4903,granular cell carcinoma,C0205644,,,MONDO:0003197,granular cell carcinoma,
+BMGC_DS03974,BMG_DS005834,,,,,,,DOID:4929,tubular adenocarcinoma,C0205645,,,MONDO:0005606,tubular adenocarcinoma,
+BMGC_DS03975,BMG_DS005835,,,,,,,DOID:6204,follicular adenoma,C0205647,,,,,
+BMGC_DS03976,BMG_DS005836,,,,,,,DOID:5403,microcystic adenoma,C0205648,,,MONDO:0003435,microcystic adenoma,
+BMGC_DS03977,BMG_DS005837,,,,,,,DOID:3172,papillary adenoma,C0205650,,,MONDO:0002533,papillary adenoma,
+BMGC_DS03978,BMG_DS005838,,"Infections, Arenavirus",Arenaviridae Infections,,,,,,C0205671,D001117,,MONDO:0005650,Arenaviridae infectious disease,
+BMGC_DS03979,BMG_DS005840,,,,,,,DOID:4015,sarcomatoid carcinoma,C0205697,,,MONDO:0006406,sarcomatoid carcinoma,
+BMGC_DS03980,BMG_DS005843,,Alpers Syndrome,Diffuse Cerebral Sclerosis of Schilder,,,,DOID:0080122,Alpers-Huttenlocher syndrome,C0205710,D002549,203700,MONDO:0008758,mitochondrial DNA depletion syndrome 4a,
+BMGC_DS03981,BMG_DS005844,,Pelizaeus-Merzbacher Disease,Pelizaeus-Merzbacher Disease,,,,DOID:3210,Pelizaeus-Merzbacher disease,C0205711,D020371,312080,MONDO:0010714,Pelizeaus-Merzbacher spectrum disorder,
+BMGC_DS03982,BMG_DS005845,,,,,,,,,C0205713,,180800,MONDO:0008392,Roussy-Levy syndrome,
+BMGC_DS03983,BMG_DS005847,,"Diabetes, Autoimmune","Diabetes Mellitus, Type 1",,,,,,C0205734,D003922,,,,
+BMGC_DS03984,BMG_DS005849,,,,,,,DOID:10041,dysplastic nevus syndrome,C0205747,,,,,
+BMGC_DS03985,BMG_DS005850,,Chronic Cystic Mastitis,Fibrocystic Breast Disease,,,,,,C0205765,D005348,,,,
+BMGC_DS03986,BMG_DS005851,,,,,,,,,C0205766,,,MONDO:0037745,fibromyxoid tumor,
+BMGC_DS03987,BMG_DS005852,,,,,,,DOID:5077,subependymal giant cell astrocytoma,C0205768,,,MONDO:0016693,subependymal giant cell astrocytoma,
+BMGC_DS03988,BMG_DS005853,,,,,,,DOID:5075,myxopapillary ependymoma,C0205769,,,MONDO:0016699,myxopapillary ependymoma,
+BMGC_DS03989,BMG_DS005854,,,,,,,DOID:2626,choroid plexus papilloma,C0205770,,260500,MONDO:0009837,choroid plexus papilloma,
+BMGC_DS03990,BMG_DS005855,,,,,,,DOID:474,histiocytoid hemangioma,C0205788,,,MONDO:0021169,epithelioid hemangioma,
+BMGC_DS03991,BMG_DS005856,,,,,,,DOID:468,intramuscular hemangioma,C0205789,,,MONDO:0003088,intramuscular hemangioma,
+BMGC_DS03992,BMG_DS005857,,,,,,,DOID:1283,enterocele,C0205792,,,,,
+BMGC_DS03993,BMG_DS005858,,,,,,,DOID:5264,epithelioid leiomyosarcoma,C0205815,,,MONDO:0003356,epithelioid leiomyosarcoma,
+BMGC_DS03994,BMG_DS005859,,,,,,,DOID:5268,myxoid leiomyosarcoma,C0205816,,,MONDO:0003359,myxoid leiomyosarcoma,
+BMGC_DS03995,BMG_DS005861,,,,,,,DOID:10192,pleomorphic lipoma,C0205823,,,MONDO:0000966,pleomorphic lipoma,
+BMGC_DS03996,BMG_DS005862,,,,,,,,,C0205824,,,MONDO:0020563,dedifferentiated liposarcoma,
+BMGC_DS03997,BMG_DS005863,,,,,,,DOID:5702,pleomorphic liposarcoma,C0205825,,,MONDO:0020562,pleomorphic liposarcoma,
+BMGC_DS03998,BMG_DS005865,,,,,,,DOID:3861,medullomyoblastoma,C0205833,,,MONDO:0006300,medullomyoblastoma with myogenic differentiation,
+BMGC_DS03999,BMG_DS005866,,,,,,,DOID:2994,germ cell cancer,C0205851,,,MONDO:0005040,germ cell tumor,
+BMGC_DS04000,BMG_DS005869,,,,,,,DOID:139,squamous cell papilloma,C0205874,,,MONDO:0001825,squamous papilloma,
+BMGC_DS04001,BMG_DS005870,,,,,,,DOID:2615,papilloma,C0205875,,,MONDO:0021098,papillomatosis,
+BMGC_DS04002,BMG_DS005872,,,,,,,DOID:1664,pineoblastoma,C0205898,,,MONDO:0016722,pineoblastoma,
+BMGC_DS04003,BMG_DS005874,7359008;203490000,Algoneurodystrophy,,FB86.Z,"Disorders associated with bone growth, unspecified",M89.0,DOID:14022,algoneurodystrophy,C0205930,,,MONDO:0001859,algoneurodystrophy,Algoneurodystrophy | Algoneurodystrophy (disorder) | Reflex sympathetic dystrophy | RSD - Reflex sympathetic dystrophy | Algoneurodystrophy | Algodystrophy | CRPS - Complex regional pain syndrome type I | Complex regional pain syndrome type I | Reflex sympathetic dystrophy (disorder)
+BMGC_DS04004,BMG_DS005875,,,,,,,DOID:6193,epithelioid sarcoma,C0205944,,,MONDO:0017387,epithelioid sarcoma,
+BMGC_DS04005,BMG_DS005876,,,,,,,DOID:4235,spindle cell sarcoma,C0205945,,,MONDO:0002927,spindle cell sarcoma,
+BMGC_DS04006,BMG_DS005877,,,,,,,DOID:3284,thymic carcinoma,C0205969,,,MONDO:0006451,thymic carcinoma,
+BMGC_DS04007,BMG_DS005878,,HIV Encephalopathy,AIDS Dementia Complex,,,,,,C0206019,D015526,,,,
+BMGC_DS04008,BMG_DS005879,,Fatal Familial Insomnia,"Insomnia, Fatal Familial",,,,DOID:0050433,fatal familial insomnia,C0206042,D034062,600072,MONDO:0010808,fatal familial insomnia,
+BMGC_DS04009,BMG_DS005880,,"Infections, Calicivirus",Caliciviridae Infections,,,,,,C0206044,D017250,,MONDO:0005687,Caliciviridae infectious disease,
+BMGC_DS04010,BMG_DS005881,115664001;90128006,Photoallergy,"Dermatitis, Photoallergic",,,,,,C0206051,D017454,,,,Immunologic photosensitivity | Allergic photosensitivity | Photoallergy | Photoallergy (disorder) | Photosensitivity | Photosensitivity (finding) | Photosensitivity of skin
+BMGC_DS04011,BMG_DS005882,,"Pneumonia, Interstitial","Lung Diseases, Interstitial",,,,,,C0206061,D017563,,,,
+BMGC_DS04012,BMG_DS005883,,"Lung Diseases, Interstitial","Lung Diseases, Interstitial",,,,DOID:3082,interstitial lung disease,C0206062,D017563,,,,
+BMGC_DS04013,BMG_DS005884,,Microvascular Angina,Microvascular Angina,,,,,,C0206064,D017566,,MONDO:0044875,coronary microvascular disorder,
+BMGC_DS04014,BMG_DS005885,,Focal Epithelial Hyperplasia,Focal Epithelial Hyperplasia,,,,DOID:5362,focal epithelial hyperplasia,C0206067,D017573,229045,MONDO:0009237,focal epithelial hyperplasia,
+BMGC_DS04015,BMG_DS005886,237793004,Hyperandrogenism,Hyperandrogenism,,,,DOID:11613,hyperandrogenism,C0206081,D017588,MTHU024060,MONDO:0001324,obsolete hyperandrogenism,Hyperandrogenism | Hyperandrogenisation syndrome | Hyperandrogenization syndrome | Hyperandrogenization syndrome (disorder)
+BMGC_DS04016,BMG_DS005887,,"Myelinolysis, Central Pontine","Myelinolysis, Central Pontine",,,,DOID:636,central pontine myelinolysis,C0206083,D017590,,MONDO:0006692,central pontine myelinolysis,
+BMGC_DS04017,BMG_DS005888,,Kleine-Levin Syndrome,Kleine-Levin Syndrome,,,,DOID:0060165,Kleine-Levin syndrome,C0206085,D017593,148840,MONDO:0007863,Kleine-Levin syndrome,
+BMGC_DS04018,BMG_DS005889,,,,,,,DOID:171,neuroectodermal tumor,C0206093,,,,,
+BMGC_DS04019,BMG_DS005892,,WAGR Syndrome,WAGR Syndrome,,,,DOID:14515,WAGR syndrome,C0206115,D017624,194072,MONDO:0008681,WAGR syndrome,
+BMGC_DS04020,BMG_DS005893,,CREST Syndrome,CREST Syndrome,,,,DOID:0060218,CREST syndrome,C0206138,D017675,,MONDO:0019563,CREST syndrome,
+BMGC_DS04021,BMG_DS005894,,"Lichen Planus, Oral","Lichen Planus, Oral",,,,,,C0206139,D017676,,MONDO:0043923,"lichen planus, oral",
+BMGC_DS04022,BMG_DS005895,,Idiopathic Hypereosinophilic Syndrome,Hypereosinophilic Syndrome,,,,,,C0206141,D017681,607685,MONDO:0011895,idiopathic hypereosinophilic syndrome,
+BMGC_DS04023,BMG_DS005896,,Loeffler's Endocarditis,Hypereosinophilic Syndrome,,,,,,C0206143,D017681,,MONDO:0019159,Loeffler endocarditis,
+BMGC_DS04024,BMG_DS005897,,Stunned Myocardium,Myocardial Stunning,,,,,,C0206145,D017682,,,,
+BMGC_DS04025,BMG_DS005898,,Myocardial Stunning,Myocardial Stunning,,,,DOID:9767,myocardial stunning,C0206146,D017682,,MONDO:0004876,myocardial stunning,
+BMGC_DS04026,BMG_DS005900,,"Myopathies, Nemaline","Myopathies, Nemaline",,,,DOID:3191,nemaline myopathy,C0206157,D017696,,MONDO:0018958,nemaline myopathy,
+BMGC_DS04027,BMG_DS005901,,Community-Acquired Infections,Community-Acquired Infections,,,,,,C0206171,D017714,,,,
+BMGC_DS04028,BMG_DS005903,,Cytomegalovirus Retinitis,Cytomegalovirus Retinitis,,,,DOID:0080160,Cytomegalovirus retinitis,C0206178,D017726,,MONDO:0000878,cytomegalovirus retinitis,
+BMGC_DS04029,BMG_DS005904,,,,,,,,,C0206180,,,MONDO:0020325,anaplastic large cell lymphoma,
+BMGC_DS04030,BMG_DS005905,,,,,,,,,C0206182,,,MONDO:0020326,lymphomatoid papulosis,
+BMGC_DS04031,BMG_DS005906,,,,,,,DOID:0060315,oral hairy leukoplakia,C0206186,,,MONDO:0000743,oral hairy leukoplakia,
+BMGC_DS04032,BMG_DS005909,,"Amyloid Neuropathies, Familial","Amyloid Neuropathies, Familial",,,,,,C0206245,D028227,,MONDO:0007100,familial amyloid neuropathy,
+BMGC_DS04033,BMG_DS005910,,Amyloid Neuropathies,Amyloid Neuropathies,,,,,,C0206247,D017772,,,,
+BMGC_DS04034,BMG_DS005912,,Canavan Disease,Canavan Disease,,,,DOID:3613,Canavan disease,C0206307,D017825,271900,MONDO:0010079,Canavan disease,
+BMGC_DS04035,BMG_DS005913,,Exfoliation Syndrome,Exfoliation Syndrome,,,,DOID:13641,exfoliation syndrome,C0206368,D017889,,MONDO:0008327,exfoliation syndrome,
+BMGC_DS04036,BMG_DS005915,,"Tuberculosis, Drug-Resistant","Tuberculosis, Multidrug-Resistant",,,,,,C0206525,D018088,,MONDO:0041806,drug-resistant tuberculosis,
+BMGC_DS04037,BMG_DS005916,,"Tuberculosis, Multidrug-Resistant","Tuberculosis, Multidrug-Resistant",,,,DOID:401,multidrug-resistant tuberculosis,C0206526,D018088,,MONDO:0005861,multidrug-resistant tuberculosis,
+BMGC_DS04038,BMG_DS005918,,Endolymphatic Hydrops,Endolymphatic Hydrops,,,,DOID:9848,endolymphatic hydrops,C0206586,D018159,,MONDO:0006744,endolymphatic hydrops,
+BMGC_DS04039,BMG_DS005924,,Flavivirus Infections,Flavivirus Infections,,,,,,C0206608,D018177,,,,
+BMGC_DS04040,BMG_DS005930,,Cardiovirus Infections,Cardiovirus Infections,,,,,,C0206617,D018188,,MONDO:0005691,cardiovirus infectious disease,
+BMGC_DS04041,BMG_DS005932,,,,,,,DOID:3081,cystic lymphangioma,C0206620,,257350,MONDO:0009761,cystic hygroma,
+BMGC_DS04042,BMG_DS005933,,,,,,,DOID:2609,adenomyoma,C0206622,,,MONDO:0005635,adenomyoma,
+BMGC_DS04043,BMG_DS005934,,,,,,,DOID:4830,adenosquamous carcinoma,C0206623,,,MONDO:0006074,adenosquamous carcinoma,
+BMGC_DS04044,BMG_DS005935,,,,,,,DOID:687,hepatoblastoma,C0206624,,,MONDO:0018666,hepatoblastoma,
+BMGC_DS04045,BMG_DS005936,,,,,,,DOID:154,mixed cell type cancer,C0206625,,,MONDO:0005853,malignant mixed neoplasm,
+BMGC_DS04046,BMG_DS005937,,,,,,,DOID:4236,carcinosarcoma,C0206627,,,,,
+BMGC_DS04047,BMG_DS005939,,,,,,,DOID:4765,pulmonary blastoma,C0206629,,,MONDO:0005933,pulmonary blastoma,
+BMGC_DS04048,BMG_DS005940,,,,,,,DOID:4226,endometrial stromal sarcoma,C0206630,,,MONDO:0006745,endometrioid stromal sarcoma,
+BMGC_DS04049,BMG_DS005941,,,,,,,DOID:3315,lipoma,C0206631,,,MONDO:0021354,tumor of adipose tissue,
+BMGC_DS04050,BMG_DS005942,,,,,,,DOID:3616,angiolipoma,C0206632,,,MONDO:0006085,angiolipoma,
+BMGC_DS04051,BMG_DS005943,,,,,,,DOID:3314,angiomyolipoma,C0206633,,,MONDO:0002603,angiomyolipoma,
+BMGC_DS04052,BMG_DS005944,,,,,,,DOID:5363,myxoid liposarcoma,C0206634,,613488,MONDO:0013280,myxoid liposarcoma,
+BMGC_DS04053,BMG_DS005946,,,,,,,DOID:4545,mesenchymal chondrosarcoma,C0206637,,,MONDO:0006853,mesenchymal chondrosarcoma,
+BMGC_DS04054,BMG_DS005947,,,,,,,DOID:4305,bone giant cell tumor,C0206638,,,MONDO:0005674,bone giant cell tumor,
+BMGC_DS04055,BMG_DS005948,,,,,,,DOID:3347,osteosarcoma,C0206639,,,,,
+BMGC_DS04056,BMG_DS005950,,,,,,,DOID:3373,parosteal osteosarcoma,C0206642,,,MONDO:0006817,juxtacortical osteosarcoma,
+BMGC_DS04057,BMG_DS005951,,,,,,,DOID:3355,fibrosarcoma,C0206643,,,MONDO:0006209,fibroblastic neoplasm,
+BMGC_DS04058,BMG_DS005952,,,,,,,DOID:4415,fibrous histiocytoma,C0206644,,,MONDO:0002989,benign fibrous histiocytoma,
+BMGC_DS04059,BMG_DS005953,,,,,,,DOID:3507,dermatofibrosarcoma protuberans,C0206647,,,,,
+BMGC_DS04060,BMG_DS005955,,,,,,,DOID:1618,breast fibroadenoma,C0206650,,,,,
+BMGC_DS04061,BMG_DS005956,,,,,,,DOID:4233,clear cell sarcoma,C0206651,,,MONDO:0002926,clear cell sarcoma,
+BMGC_DS04062,BMG_DS005957,,,,,,,DOID:3098,small cell sarcoma,C0206652,,,MONDO:0006974,small cell sarcoma,
+BMGC_DS04063,BMG_DS005958,,,,,,,DOID:4265,angiomyoma,C0206653,,,MONDO:0006646,angioleiomyoma,
+BMGC_DS04064,BMG_DS005959,,,,,,,DOID:5138,leiomyomatosis,C0206654,,,MONDO:0003295,leiomyomatosis,
+BMGC_DS04065,BMG_DS005960,,,,,,,DOID:4051,alveolar rhabdomyosarcoma,C0206655,,268220,MONDO:0009994,alveolar rhabdomyosarcoma,
+BMGC_DS04066,BMG_DS005961,,,,,,,DOID:3246,embryonal rhabdomyosarcoma,C0206656,,268210,MONDO:0009993,embryonal rhabdomyosarcoma,
+BMGC_DS04067,BMG_DS005962,,,,,,,DOID:4239,alveolar soft part sarcoma,C0206657,,606243,MONDO:0011655,alveolar soft part sarcoma,
+BMGC_DS04068,BMG_DS005963,,,,,,,DOID:4310,smooth muscle tumor,C0206658,,,MONDO:0006975,smooth muscle tumor,
+BMGC_DS04069,BMG_DS005964,,,,,,,DOID:3308,embryonal carcinoma,C0206659,,,MONDO:0005440,embryonal carcinoma,
+BMGC_DS04070,BMG_DS005965,,,,,,,DOID:3304,germinoma,C0206660,,,MONDO:0002598,germinoma,
+BMGC_DS04071,BMG_DS005967,,,,,,,DOID:0050902,medulloblastoma,C0206663,,,MONDO:0005462,primitive neuroectodermal tumor,
+BMGC_DS04072,BMG_DS005968,,,,,,,DOID:3305,teratocarcinoma,C0206664,,,MONDO:0002599,teratocarcinoma,
+BMGC_DS04073,BMG_DS005969,,,,,,,DOID:3596,placental site trophoblastic tumor,C0206666,,,MONDO:0020552,placental site trophoblastic tumor,
+BMGC_DS04074,BMG_DS005970,,,,,,,,,C0206667,,,MONDO:0003924,adrenal cortex adenoma,
+BMGC_DS04075,BMG_DS005971,,,,,,,,,C0206669,,,MONDO:0018902,hepatocellular adenoma,
+BMGC_DS04076,BMG_DS005972,,,,,,,DOID:5442,eccrine acrospiroma,C0206671,,,MONDO:0006738,eccrine acrospiroma,
+BMGC_DS04077,BMG_DS005973,,,,,,,DOID:3893,hidrocystoma,C0206672,,,MONDO:0006787,hidrocystoma,
+BMGC_DS04078,BMG_DS005974,,,,,,,DOID:2065,syringoma,C0206673,,,MONDO:0002191,syringoma,
+BMGC_DS04079,BMG_DS005975,,,,,,,,,C0206674,,,MONDO:0000502,villous adenoma,
+BMGC_DS04080,BMG_DS005976,,,,,,,DOID:746,adenomatoid tumor,C0206675,,,MONDO:0004230,adenomatoid tumor,
+BMGC_DS04081,BMG_DS005977,,,,,,,DOID:4468,clear cell adenocarcinoma,C0206681,,,MONDO:0005004,clear cell adenocarcinoma,
+BMGC_DS04082,BMG_DS005978,,,,,,,DOID:3962,follicular thyroid carcinoma,C0206682,,,MONDO:0005034,thyroid gland follicular carcinoma,
+BMGC_DS04083,BMG_DS005980,,,,,,,DOID:4839,sebaceous adenocarcinoma,C0206684,,,MONDO:0006962,sebaceous adenocarcinoma,
+BMGC_DS04084,BMG_DS005981,,,,,,,DOID:3025,acinar cell carcinoma,C0206685,,,MONDO:0004965,acinar cell carcinoma,
+BMGC_DS04085,BMG_DS005982,,,,,,,DOID:3948,adrenocortical carcinoma,C0206686,,,MONDO:0006639,adrenal cortex carcinoma,
+BMGC_DS04086,BMG_DS005983,,,,,,,DOID:2871,endometrial carcinoma,C0206687,,,,,
+BMGC_DS04087,BMG_DS005984,,,,,,,DOID:3457,invasive lobular carcinoma,C0206692,,,MONDO:0000552,breast lobular carcinoma,
+BMGC_DS04088,BMG_DS005985,,,,,,,DOID:4531,mucoepidermoid carcinoma,C0206694,,,MONDO:0003036,mucoepidermoid carcinoma,
+BMGC_DS04089,BMG_DS005986,,,,,,,DOID:1800,neuroendocrine carcinoma,C0206695,,,MONDO:0002120,neuroendocrine carcinoma,
+BMGC_DS04090,BMG_DS005987,,,,,,,DOID:3493,signet ring cell adenocarcinoma,C0206696,,,MONDO:0005092,signet ring cell carcinoma,
+BMGC_DS04091,BMG_DS005989,,,,,,,DOID:4947,cholangiocarcinoma,C0206698,,,MONDO:0019087,cholangiocarcinoma,
+BMGC_DS04092,BMG_DS005990,,,,,,,DOID:3603,mucinous cystadenocarcinoma,C0206699,,,MONDO:0005858,mucinous cystadenocarcinoma,
+BMGC_DS04093,BMG_DS005991,,,,,,,DOID:3110,papillary cystadenocarcinoma,C0206700,,,MONDO:0005074,papillary cystadenocarcinoma,
+BMGC_DS04094,BMG_DS005992,,,,,,,DOID:3114,serous cystadenocarcinoma,C0206701,,,MONDO:0024621,serous cystadenocarcinoma,
+BMGC_DS04095,BMG_DS005993,,,,,,,DOID:4927,Klatskin's tumor,C0206702,,,MONDO:0003345,hilar cholangiocarcinoma,
+BMGC_DS04096,BMG_DS005994,,,,,,,DOID:5583,lung giant cell carcinoma,C0206703,,,,,
+BMGC_DS04097,BMG_DS005995,,,,,,,DOID:4552,large cell carcinoma,C0206704,,,MONDO:0005232,large cell carcinoma,
+BMGC_DS04098,BMG_DS005996,,,,,,,DOID:3737,verrucous carcinoma,C0206706,,,MONDO:0006006,verrucous carcinoma,
+BMGC_DS04099,BMG_DS005999,,,,,,,DOID:2513,basal cell carcinoma,C0206710,,,MONDO:0020799,basal cell neoplasm,
+BMGC_DS04100,BMG_DS006000,,,,,,,DOID:5374,pilomatrixoma,C0206711,,132600,MONDO:0007564,pilomatrixoma,
+BMGC_DS04101,BMG_DS006001,,,,,,,DOID:1627,intraductal papilloma,C0206713,,,MONDO:0002060,intraductal papilloma,
+BMGC_DS04102,BMG_DS006003,,,,,,,DOID:5078,ganglioglioma,C0206716,,,MONDO:0016733,ganglioglioma,
+BMGC_DS04103,BMG_DS006004,,,,,,,DOID:369,olfactory neuroblastoma,C0206717,,,MONDO:0016029,esthesioneuroblastoma,
+BMGC_DS04104,BMG_DS006005,,,,,,,DOID:4163,ganglioneuroblastoma,C0206718,,,MONDO:0005035,ganglioneuroblastoma,
+BMGC_DS04105,BMG_DS006006,,,,,,,DOID:14174,central neurocytoma,C0206719,,,MONDO:0019134,central neurocytoma,
+BMGC_DS04106,BMG_DS006007,,,,,,,DOID:3168,squamous cell neoplasm,C0206720,,,MONDO:0002532,squamous cell neoplasm,
+BMGC_DS04107,BMG_DS006008,,,,,,,DOID:3179,inverted papilloma,C0206721,,,MONDO:0002537,inverted papilloma,
+BMGC_DS04108,BMG_DS006010,,,,,,,DOID:2997,Sertoli-Leydig cell tumor,C0206723,,,MONDO:0002479,Sertoli-Leydig cell tumor,
+BMGC_DS04109,BMG_DS006011,,,,,,,DOID:192,sex cord-gonadal stromal tumor,C0206724,,,MONDO:0006055,sex cord-stromal tumor,
+BMGC_DS04110,BMG_DS006012,,,,,,,DOID:4843,subependymal glioma,C0206725,,,MONDO:0007667,subependymoma,
+BMGC_DS04111,BMG_DS006013,,,,,,,DOID:3071,gliosarcoma,C0206726,,,MONDO:0016681,gliosarcoma,
+BMGC_DS04112,BMG_DS006014,,,,,,,DOID:1192,peripheral nervous system neoplasm,C0206727,,,MONDO:0002547,nerve sheath neoplasm,
+BMGC_DS04113,BMG_DS006015,,,,,,,DOID:5151,plexiform neurofibroma,C0206728,,,MONDO:0003304,plexiform neurofibroma,
+BMGC_DS04114,BMG_DS006016,,,,,,,DOID:3512,neurofibrosarcoma,C0206729,,,MONDO:0002675,neurofibrosarcoma,
+BMGC_DS04115,BMG_DS006018,,,,,,,DOID:2725,capillary hemangioma,C0206733,,,MONDO:0002407,capillary hemangioma,
+BMGC_DS04116,BMG_DS006019,,,,,,,DOID:5241,hemangioblastoma,C0206734,,,MONDO:0016748,hemangioblastoma,
+BMGC_DS04117,BMG_DS006020,,,,,,,DOID:4359,amelanotic melanoma,C0206735,,,MONDO:0002971,amelanotic melanoma,
+BMGC_DS04118,BMG_DS006021,,,,,,,,,C0206736,,,MONDO:0006680,blue nevus,
+BMGC_DS04119,BMG_DS006024,,,,,,,,,C0206739,,,MONDO:0044793,spitz nevus,
+BMGC_DS04120,BMG_DS006025,,,,,,,DOID:3672,rhabdoid cancer,C0206743,,,MONDO:0002728,rhabdoid tumor,
+BMGC_DS04121,BMG_DS006026,,"T-Lymphocytopenia, Idiopathic CD4-Positive","T-Lymphocytopenia, Idiopathic CD4-Positive",,,,DOID:3109,idiopathic CD4-positive T-lymphocytopenia,C0206744,D018344,,MONDO:0005807,idiopathic CD4-positive T-lymphocytopenia,
+BMGC_DS04122,BMG_DS006028,,Coronavirus Infections,Coronavirus Infections,,,,,,C0206750,D018352,,MONDO:0005719,Coronavinae infectious disease,
+BMGC_DS04123,BMG_DS006032,,,,,,,DOID:169,neuroendocrine tumor,C0206754,,,MONDO:0019496,neuroendocrine neoplasm,
+BMGC_DS04124,BMG_DS006033,,,,,,,,,C0206762,,,MONDO:0017427,congenital deformities of limbs,
+BMGC_DS04125,BMG_DS006036,,,,,,,DOID:2068,Bartholin's gland benign neoplasm,C0220616,,,MONDO:0021114,Bartholin gland neoplasm,
+BMGC_DS04126,BMG_DS006038,,,,,,,DOID:1319,brain cancer,C0220624,,,,,
+BMGC_DS04127,BMG_DS006039,,,,,,,DOID:6039,uveal melanoma,C0220633,,155720,MONDO:0006486,uveal melanoma,
+BMGC_DS04128,BMG_DS006040,,,,,,,,,C0220636,,,MONDO:0004669,salivary gland cancer,
+BMGC_DS04129,BMG_DS006041,,,,,,,,,C0220641,,,MONDO:0023644,lip and oral cavity carcinoma,
+BMGC_DS04130,BMG_DS006045,,Pfeiffer Syndrome,Acrocephalosyndactylia,,,,DOID:14705,Pfeiffer syndrome,C0220658,D000168,101600,MONDO:0007043,Pfeiffer syndrome,
+BMGC_DS04131,BMG_DS006046,66758006,Acrodysostosis,,,,,DOID:14669,acrodysostosis,C0220659,C538179,MTHU039921,MONDO:0019797,acrodysostosis,Acrodysostosis | Acrodysostosis (disorder)
+BMGC_DS04132,BMG_DS006047,,,,,,,,,C0220660,,102650,MONDO:0007062,"adactylia, unilateral",
+BMGC_DS04133,BMG_DS006048,,"ARTHROGRYPOSIS, DISTAL, TYPE 1",,,,,,,C0220662,,108120,MONDO:0007157,"arthrogryposis, distal, type 1A",
+BMGC_DS04134,BMG_DS006049,,"Blepharophimosis, Ptosis, and Epicanthus Inversus",,,,,DOID:14778,"blepharophimosis, ptosis, and epicanthus inversus syndrome",C0220663,C562419,110100,MONDO:0007201,"blepharophimosis, ptosis, and epicanthus inversus syndrome",
+BMGC_DS04135,BMG_DS006050,,,,,,,,,C0220664,,113200,MONDO:0007222,brachydactyly type D,
+BMGC_DS04136,BMG_DS006051,,"ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA",,,,,,,C0220666,,114300,MONDO:0007252,Gordon syndrome,
+BMGC_DS04137,BMG_DS006052,,,,,,,DOID:0111595,congenital contractural arachnodactyly,C0220668,,121050,MONDO:0007363,congenital contractural arachnodactyly,
+BMGC_DS04138,BMG_DS006053,,,,,,,DOID:14777,benign familial neonatal epilepsy,C0220669,,,MONDO:0016027,benign neonatal seizures,
+BMGC_DS04139,BMG_DS006055,,Goldenhar Syndrome with Ipsilateral Radial Defect,Goldenhar Syndrome,,,,,,C0220681,D006053,141400,MONDO:0007712,oculoauriculovertebral spectrum with radial defects,
+BMGC_DS04140,BMG_DS006056,,,,,,,,,C0220685,,200610,MONDO:0008702,achondrogenesis type II,
+BMGC_DS04141,BMG_DS006057,,Aase Smith syndrome,,,,,,,C0220686,C535332,147800,MONDO:0007839,Aase-Smith syndrome,
+BMGC_DS04142,BMG_DS006058,711156009,KBG syndrome,,,,,DOID:14780,KBG syndrome,C0220687,C537015,148050,MONDO:0007846,KBG syndrome,"Short stature-characteristic facies-mental retardation-macrodontia-skeletal anomalies syndrome | KBG syndrome | Short stature, facial and skeletal anomalies, intellectual disability, macrodontia syndrome (disorder) | Short stature, facial and skeletal anomalies, intellectual disability, macrodontia syndrome"
+BMGC_DS04143,BMG_DS006059,,,,,,,,,C0220690,,153470,MONDO:0007923,"macrocephaly, benign familial",
+BMGC_DS04144,BMG_DS006060,,"Maxillonasal dysplasia, Binder type",,,,,DOID:14683,Binder syndrome,C0220692,C536036,155050,MONDO:0007953,Binder syndrome,
+BMGC_DS04145,BMG_DS006061,,Microcephaly autosomal dominant,,,,,DOID:14725,autosomal dominant microcephaly,C0220693,C537323,156580,MONDO:0007988,autosomal dominant primary microcephaly,
+BMGC_DS04146,BMG_DS006063,,,,,,,DOID:1148,polydactyly,C0220697,,,MONDO:0020927,postaxial polydactyly,
+BMGC_DS04147,BMG_DS006064,,RETINITIS PIGMENTOSA 1,,,,,DOID:10584,retinitis pigmentosa,C0220701,,180100;603937,MONDO:0008377,retinitis pigmentosa 1,
+BMGC_DS04148,BMG_DS006065,,,,,,,,,C0220702,,181510,MONDO:0008414,schizophrenia 1,
+BMGC_DS04149,BMG_DS006066,205642004;83092002,Shprintzen syndrome,,,,,DOID:12583,velocardiofacial syndrome,C0220704,,192430,MONDO:0008644,velocardiofacial syndrome,Shprintzen syndrome | Shprintzen syndrome (disorder) | Shprintzen syndrome | Velo-cardio-facial syndrome | Shprintzen syndrome (disorder) | Velocardiofacial syndrome | VCF-Velocardiofacial syndrome | 22q11 microdeletion with velocardiofacial syndrome phenotype
+BMGC_DS04150,BMG_DS006067,,,,,,,DOID:14679,VACTERL association,C0220708,,,,,
+BMGC_DS04151,BMG_DS006068,74351001;128596003,Medium-chain acyl-coenzyme A dehydrogenase deficiency,,,,,,,C0220710,,201450,MONDO:0008721,medium chain acyl-CoA dehydrogenase deficiency,Reye's syndrome | Reye's encephalopathy | Reye's syndrome (disorder) | Reye syndrome | MCAD deficiency | Medium-chain acyl-coenzyme A dehydrogenase deficiency | MCAD - Medium chain acyl-CoA dehydrogenase deficiency | Medium chain acyl-CoA dehydrogenase deficiency | Medium-chain acyl-coenzyme A dehydrogenase deficiency (disorder)
+BMGC_DS04152,BMG_DS006069,237996001,Long chain acyl-CoA dehydrogenase deficiency,,,,,,,C0220711,,,MONDO:0020531,long chain acyl-CoA dehydrogenase deficiency,Long chain acyl-CoA dehydrogenase deficiency | LCAD - Long chain acyl-CoA dehydrogenase deficiency | Long chain acyl-coenzyme A dehydrogenase deficiency | Long chain acyl-coenzyme A dehydrogenase deficiency (disorder)
+BMGC_DS04153,BMG_DS006070,,"CATARACT 46, JUVENILE-ONSET, WITH OR WITHOUT ARRHYTHMIC CARDIOMYOPATHY",,,,,,,C0220721,,616312;212500,MONDO:0008925,cataract 46 juvenile-onset,
+BMGC_DS04154,BMG_DS006071,,Cerebrooculofacioskeletal Syndrome 1,,,,,,,C0220722,C562434,214150,MONDO:0008955,cerebrooculofacioskeletal syndrome 1,
+BMGC_DS04155,BMG_DS006072,,,,,,,DOID:9574,choanal atresia,C0220723,,,,,
+BMGC_DS04156,BMG_DS006073,,,,,,,,,C0220724,,217100,MONDO:0015167,amniotic band syndrome,
+BMGC_DS04157,BMG_DS006074,58561002,Diastrophic dysplasia,,LD24.03,Diastrophic dysplasia,Q77.5,DOID:14687,diastrophic dysplasia,C0220726,C536170,222600,MONDO:0009107,diastrophic dysplasia,Diastrophic dysplasia | Diastrophic nanism syndrome | Diastrophic dwarf | Diastrophic dysplasia (disorder) | DTD - Diastrophic dysplasia | Diastrophic dysplasia syndrome | DD - Diastrophic dysplasia | Diastrophic dwarfism
+BMGC_DS04158,BMG_DS006075,702432006,Fryns syndrome,,,,,,,C0220730,C538070,229850,MONDO:0009253,Fryns syndrome,"Diaphragmatic hernia, abnormal face and distal limb anomalies (disorder) | Fryns syndrome | Diaphragmatic hernia, abnormal face and distal limb anomalies"
+BMGC_DS04159,BMG_DS006077,721836009,Bixler Christian Gorlin syndrome,,,,,DOID:14670,"hypertelorism, microtia, facial clefting syndrome",C0220742,C537632,239800,MONDO:0009404,"hypertelorism, microtia, facial clefting syndrome","Hypertelorism with microtia and facial clefting syndrome (disorder) | Hypertelorism with microtia and facial clefting syndrome | Bixler Christian Gorlin syndrome | HMC (hypertelorism, microtia, clefting) syndrome"
+BMGC_DS04160,BMG_DS006078,30174008,Childhood hypophosphatasia (disorder),,,,,DOID:14213,hypophosphatasia,C0220743,,,,,"Childhood hypophosphatasia | Hypophosphatasia, childhood type | Juvenile hypophosphatasia | Childhood hypophosphatasia (disorder)"
+BMGC_DS04161,BMG_DS006079,,,,,,,DOID:14671,multiple intestinal atresia,C0220744,,,MONDO:0009465,multiple intestinal atresia,
+BMGC_DS04162,BMG_DS006080,,Cartilage-hair hypoplasia,,,,,DOID:14773,cartilage-hair hypoplasia,C0220748,C535916,250250,MONDO:0009595,cartilage-hair hypoplasia,
+BMGC_DS04163,BMG_DS006082,,Biotinidase Deficiency,Biotinidase Deficiency,,,,DOID:856,biotinidase deficiency,C0220754,D028921,253260,MONDO:0009665,biotinidase deficiency,
+BMGC_DS04164,BMG_DS006083,,"Niemann-Pick Disease, Type C","Niemann-Pick Disease, Type C",,,,,,C0220756,D052556,,MONDO:0018982,Niemann-Pick disease type C,
+BMGC_DS04165,BMG_DS006084,,,,,,,DOID:14798,Blount's disease,C0220757,,188700,MONDO:0008571,"Blount disease, infantile",
+BMGC_DS04166,BMG_DS006085,,Weaver-Like Syndrome,,,,,DOID:14731,Weaver syndrome,C0220765,C562443,,,,
+BMGC_DS04167,BMG_DS006086,715421009,Craniofrontonasal dysplasia,,,,,DOID:14737,craniofrontonasal syndrome,C0220767,C536456,304110,MONDO:0010570,craniofrontonasal syndrome,Craniofrontonasal dysplasia (disorder) | Craniofrontonasal dysplasia | Craniofrontonasal syndrome
+BMGC_DS04168,BMG_DS006087,49984004,FG syndrome,,,,,DOID:14711,FG syndrome,C0220769,C537923,,MONDO:0002010,FG syndrome,FG syndrome | FG syndrome (disorder)
+BMGC_DS04169,BMG_DS006088,,"RUSSELL-SILVER SYNDROME, X-LINKED",,,,,DOID:14744,Partington syndrome,C0220775,,312780,MONDO:0010727,"Russell-silver syndrome, X-linked",
+BMGC_DS04170,BMG_DS006091,,,,,,,,,C0220981,,,MONDO:0000440,metabolic acidosis,
+BMGC_DS04171,BMG_DS006092,56051008,Ketoacidosis,Ketosis,,,,,,C0220982,D007662,MTHU012088,,,Ketoacidosis | Ketoacidosis (disorder)
+BMGC_DS04172,BMG_DS006093,16242007,Hereditary orotic aciduria,,,,,,,C0220987,,258900,MONDO:0009797,orotic aciduria,Hereditary orotic aciduria | Hereditary orotic aciduria (disorder)
+BMGC_DS04173,BMG_DS006094,190919008,Xanthinuria (disorder),,,,,DOID:0060236,xanthinuria,C0220988,,,MONDO:0000721,xanthinuria,Xanthinuria | Xanthinuria (disorder)
+BMGC_DS04174,BMG_DS006095,75659004,Acquired partial lipodystrophy,,,,,,,C0220989,,,MONDO:0012104,acquired partial lipodystrophy,Acquired partial lipodystrophy | Lipodystrophic diabetes with partial lipoatrophy | Barraquer syndrome | Barraquer-Simons syndrome | Hollander-Simons syndrome | Progressive partial lipodystrophy | Progressive lipodystrophy | Macrodystrophia lipomatosa progressiva | Partial lipoatrophy | Barraquer-Simons disease | Acquired partial lipodystrophy (disorder)
+BMGC_DS04175,BMG_DS006096,,Rotor Syndrome,"Hyperbilirubinemia, Hereditary",,,,,,C0220991,D006933,237450,MONDO:0009379,Rotor syndrome,
+BMGC_DS04176,BMG_DS006097,410058007;68458004,Histidinemia,,,,E70.41,DOID:0060168,histidinemia,C0220992,C538320,235800,MONDO:0009345,histidinemia,Histidinemia (disorder) | Histidinaemia | Histidinemia | Histidine ammonia-lyase deficiency | Histidinemia | Histidinaemia | Histidine ammonia-lyase deficiency (disorder) | Histidase deficiency
+BMGC_DS04177,BMG_DS006098,13003007,Cystathioninuria,,,,E72.19,DOID:0090142,cystathioninuria,C0220993,,219500,MONDO:0009058,cystathioninuria,Cystathioninuria | CTH - Cystathioninuria | Cystathioninuria (disorder) | Cystathionine gamma-lyase deficiency syndrome
+BMGC_DS04178,BMG_DS006099,190717000;9360008,Hyperammonemia (disorder),,,,,,,C0220994,,,,,Hyperammonemia | Hyperammonaemia | Hyperammonemia (disorder)
+BMGC_DS04179,BMG_DS006101,37429009,Hypothalamic hypothyroidism,,,,,,,C0220998,,275120,MONDO:0010140,isolated thyrotropin-releasing hormone deficiency,Hypothalamic hypothyroidism | Hypothyroidism due to TRH deficiency | Hypothalamic hypothyroidism (disorder) | Tertiary hypothyroidism
+BMGC_DS04180,BMG_DS006102,,"Hyperparathyroidism, Primary","Hyperparathyroidism, Primary",,,,DOID:11202,primary hyperparathyroidism,C0221002,D049950,,MONDO:0010837,primary hyperparathyroidism,
+BMGC_DS04181,BMG_DS006103,80660001,Mauriac's syndrome,,,,,,,C0221005,,,MONDO:0022435,Mauriac syndrome,Mauriac's syndrome | Dwarfism-hepatomegaly-obesity-juvenile diabetes syndrome | Mauriac's syndrome (disorder) | Mauriac syndrome
+BMGC_DS04182,BMG_DS006106,,Malignant Atrophic Papulosis,Malignant Atrophic Papulosis,,,,,,C0221011,D054853,602248,MONDO:0011208,malignant atrophic papulosis,
+BMGC_DS04183,BMG_DS006108,,,,,,,DOID:349,systemic mastocytosis,C0221013,,,MONDO:0016586,systemic mastocytosis,
+BMGC_DS04184,BMG_DS006112,127041004,Sickle cell-beta-thalassemia,,,,,,,C0221019,,,,,Sickle cell-beta-thalassemia | Haemoglobin S/beta thalassaemia | Double heterozygous for Hb S and beta thalassaemia | Thalassaemia with haemoglobin S disease | Double heterozygous for Hb S and beta thalassemia | Hemoglobin S/beta thalassemia | Thalassemia with hemoglobin S disease | Sickle cell-beta-thalassaemia | Sickle cell-beta-thalassemia (disorder)
+BMGC_DS04185,BMG_DS006113,61777009,Thalassemia-hemoglobin C disease,,,,,,,C0221020,,,MONDO:0016490,hemoglobin C-beta-thalassemia syndrome,Hemoglobin C-F disease | Thalassemia-hemoglobin C disease | Haemoglobin C-F disease | Thalassaemia-haemoglobin C disease | Thalassemia-hemoglobin C disease (disorder)
+BMGC_DS04186,BMG_DS006116,69295006,Cyclic neutropenia,,,,D70.4,DOID:5339,cyclic hematopoiesis,C0221023,C536227,162800,MONDO:0008090,cyclic hematopoiesis,Cyclic neutropenia | Periodic neutropenia | Cyclic neutropenia (disorder)
+BMGC_DS04187,BMG_DS006117,86635005,Kasabach-Merritt syndrome,,,,,,,C0221025,,MTHU041322;141000,MONDO:0007708,Kasabach-Merritt syndrome,Kasabach-Merritt syndrome | Thrombocytopenia-hemangioma syndrome | Thrombocytopenia-haemangioma syndrome | Kasabach-Merritt syndrome (disorder) | Haemangiomatosis with thrombocytopenia | Haemangioma-haemorrhage syndrome | Hemangioma-hemorrhage syndrome | Hemangiomatosis with thrombocytopenia | Kasabach Merritt syndrome
+BMGC_DS04188,BMG_DS006118,65880007,X-linked agammaglobulinemia,,,,,DOID:14179,X-linked agammaglobulinemia,C0221026,C537409,300755,MONDO:0010421,Bruton-type agammaglobulinemia,X-linked agammaglobulinemia | Bruton's type agammaglobulinemia | Bruton's type agammaglobulinaemia | X-linked agammaglobulinaemia | Bruton's agammaglobulinaemia | XLA - X-linked agammaglobulinaemia | Bruton's hypogammaglobulinaemia | Bruton's agammaglobulinemia | XLA - X-linked agammaglobulinemia | Bruton's hypogammaglobulinemia | X-linked agammaglobulinemia (disorder) | X linked agammaglobulinemia | X linked agammaglobulinaemia | BTK-deficiency | Bruton tyrosine kinase deficiency
+BMGC_DS04189,BMG_DS006122,35824007;286289004,Familial generalized lipodystrophy,,,,,,,C0221032,,,MONDO:0006536,congenital generalized lipodystrophy,Familial generalized lipodystrophy | Familial generalised lipodystrophy | Familial generalized lipodystrophy (disorder) | Familial generalised lipodystrophy | Generalised lipodystrophy | Lipodystrophy with muscular hypertrophy | Lipodystrophy of Berardinelli | Familial lipodystrophic diabetes | Congenital lipoatrophic diabetes | Congenital lipodystrophy | Congenital lipodystrophic diabetes | Total lipodystrophy AND acromegaloid gigantism | Berardinelli lipodystrophy syndrome | Berardinelli-Seip syndrome | Familial generalized lipodystrophy | Generalized lipodystrophy | Familial generalized lipodystrophy (disorder)
+BMGC_DS04190,BMG_DS006125,37702000,Acrodermatitis enteropathica,,5C64.2Z,"Disorders of zinc metabolism, unspecified",E83.2,DOID:0050605,acrodermatitis enteropathica,C0221036,C538178,MTHU077546;201100,MONDO:0008713,acrodermatitis enteropathica,Hereditary acrodermatitis enteropathica | Primary zinc malabsorption syndrome | Brandt syndrome | Danbolt-Closs syndrome | Hereditary acrodermatitis enterohepatica | AE - Acrodermatitis enteropathica | Primary zinc malabsorption | Danbolt-Close syndrome | Acrodermatitis enteropathica | Hereditary acrodermatitis enteropathica (disorder)
+BMGC_DS04191,BMG_DS006130,,Liddle Syndrome,Liddle Syndrome,,,,DOID:0050477,Liddle syndrome,C0221043,D056929,,MONDO:0008323,Liddle syndrome,
+BMGC_DS04192,BMG_DS006131,10091002,High output heart failure,,,,I50.83,,,C0221045,,,MONDO:0005253,high output heart failure,High output heart failure | High output heart failure (disorder)
+BMGC_DS04193,BMG_DS006132,,"Syncope, Carotid Sinus",Syncope,,,,,,C0221046,D013575,,,,
+BMGC_DS04194,BMG_DS006135,18121009,Chronic berylliosis,,,,,,,C0221052,,,MONDO:0015274,chronic beryllium disease,Chronic berylliosis | Beryllium granuloma | Chronic beryllium disease | Chronic beryllium lung | Chronic beryllium lung disease | Chronic beryllium poisoning | Chronic berylliosis (disorder)
+BMGC_DS04195,BMG_DS006137,,Welander Distal Myopathy,Distal Myopathies,,,,,,C0221054,D049310,604454,MONDO:0011466,"distal myopathy, Welander type",
+BMGC_DS04196,BMG_DS006138,,,,,,,DOID:0111538,paramyotonia congenita of Von Eulenburg,C0221055,,168300,MONDO:0008195,paramyotonia congenita of Von Eulenburg,
+BMGC_DS04197,BMG_DS006142,25044007,Subacute myelo-optic neuropathy,,,,,,,C0221059,,,,,Neuromyelitis optica | Devic's disease | Subacute myelo-optic neuropathy | Neuromyelitis optica (disorder) | Devic syndrome | Optic neuromyelitis | SMON - subacute myelo-optico-neuropathy
+BMGC_DS04198,BMG_DS006143,,Mobius Syndrome,Mobius Syndrome,,,,DOID:13501,Moebius syndrome,C0221060,D020331,157900,MONDO:0008006,Mobius syndrome,
+BMGC_DS04199,BMG_DS006144,66988006;718221007,Behr syndrome,,,,,DOID:0111580,Behr syndrome,C0221061,C537669,210000,MONDO:0008858,Behr syndrome,Abortive cerebellar ataxia | Behr's syndrome I | Infantile optic atrophy-ataxia | Abortive cerebellar ataxia (disorder) | Behr syndrome | Behr syndrome (disorder) | Behr syndrome | Infantile hereditary optic atrophy with neurological abnormality
+BMGC_DS04200,BMG_DS006145,,Subacute Combined Degeneration,Subacute Combined Degeneration,,,,,,C0221065,D052879,,,,
+BMGC_DS04201,BMG_DS006146,,Anterior Spinal Artery Syndrome,Anterior Spinal Artery Syndrome,,,,DOID:6712,anterior spinal artery syndrome,C0221069,D020759,,MONDO:0006650,anterior spinal artery syndrome,
+BMGC_DS04202,BMG_DS006147,,,,,,,DOID:9478,postpartum depression,C0221074,,,MONDO:0005929,postpartum depression,
+BMGC_DS04203,BMG_DS006151,23130000,Paroxysmal hypertension,,,,,,,C0221154,,,,,Paroxysmal hypertension | Paroxysmal hypertension (disorder) | Episodic hypertension
+BMGC_DS04204,BMG_DS006153,,,,,,,,,C0221158,,,MONDO:0017988,multifocal atrial tachycardia,
+BMGC_DS04205,BMG_DS006154,,Motor Disorders,,,,,,,C0221163,D000068079,,,,
+BMGC_DS04206,BMG_DS006157,66637005,Hemiballismus,Dyskinesias,,,,,,C0221169,D020820,,,,Hemiballism | Hemiballismus | Body of Luys syndrome | Hemiballismus-hemichorea syndrome | Hemiballism (disorder) | Hemiballism (abnormal involuntary movements)
+BMGC_DS04207,BMG_DS006159,,,,,,,,,C0221210,,193250,MONDO:0008666,volvulus of midgut,
+BMGC_DS04208,BMG_DS006163,,Centriacinar Emphysema,Pulmonary Emphysema,,,,,,C0221227,D011656,,,,
+BMGC_DS04209,BMG_DS006168,200729007;266429005;81670006;155662001;196554004,Angular cheilitis,,DA00.Z,"Disorder of lips, unspecified",K13.0,DOID:0060312,angular cheilitis,C0221237,,MTHU051337,MONDO:0000741,angular cheilitis,Angular cheilitis | Angular cheilitis (disorder) | Angular cheilitis | Angular stomatitis | Perleche | Angular cheilitis (disorder) | Perlèche | Perlèche | Angular cheilosis | Migrating cheilosis | Intertrigo labialis | Perlèche (disorder) | (Sore lip) or (angular stomatitis &/or cheilitis) | Sore lip | Angular stomatitis and cheilitis | Angular cheilitis | (Sore lip) or (angular stomatitis &/or cheilitis) (disorder)
+BMGC_DS04210,BMG_DS006169,35546006,Mesangial proliferative glomerulonephritis,,,,,DOID:4783,mesangial proliferative glomerulonephritis,C0221238,,MTHU069083,MONDO:0003139,mesangial proliferative glomerulonephritis,Mesangial proliferative glomerulonephritis | Mesangial proliferative glomerulonephritis (disorder) | Mesangioproliferative glomerulonephritis
+BMGC_DS04211,BMG_DS006170,45406000;236392004,Rapidly progressive glomerulonephritis,,,,,DOID:4776,rapidly progressive glomerulonephritis,C0221239,,,MONDO:0017236,rapidly progressive glomerulonephritis,Idiopathic crescentic glomerulonephritis | Idiopathic crescentic glomerulonephritis (disorder) | Rapidly progressive glomerulonephritis | RPGN - Rapidly progressive glomerulonephritis | Rapidly progressive glomerulonephritis (disorder)
+BMGC_DS04212,BMG_DS006173,200763009;156329007;156327009;48596006,Seborrheic dermatitis of scalp,,,,,DOID:8941,seborrheic infantile dermatitis,C0221244,,,,,Seborrheic dermatitis of scalp | Seborrhoeic dermatitis of scalp | Seborrhoeic dermatitis of scalp (disorder) | Seborrhoeic dermatitis of scalp | Seborrheic dermatitis of scalp | Seborrheic dermatitis of scalp (disorder) | Seborrhoeic eczema of scalp | Seborrhoea capitis | Seborrhea capitis | Seborrheic eczema of scalp | Seborrhoeic dermatitis of scalp | Seborrheic dermatitis of scalp | Seborrhoeic dermatitis of scalp (disorder) | Pityriasis simplex | Pityriasis streptogenes | Scurfiness of scalp | Dandruff | Scurf | Pityriasis capitis | Pityriasis sicca | Seborrhea capitis | Seborrheic dermatitis of scalp | Seborrheic eczema of scalp | Seborrhea sicca | Seborrhoea capitis | Seborrhoea sicca | Seborrhoeic eczema of scalp | Seborrhoeic dermatitis of scalp | Scurfiness of scalp (disorder)
+BMGC_DS04213,BMG_DS006176,60332004;156412005;267864001;193927000,Trichiasis,Trichiasis,,,,,,C0221259,D058457,MTHU017606,,,Trichiasis | Trichiasis (disorder) | Malposition of eyelashes | (Hair/hair follicle disease NOS) or (ingrowing hair) or (trichiasis) or (Wuchereria infestation) | Trichiasis | Wuchereria infestation | Ingrowing hair | Hair/hair follicle disease NOS | (Hair/hair follicle disease NOS) or (ingrowing hair) or (trichiasis) or (Wuchereria infestation) (disorder) | (Hair/hair follicle disease NOS) or (ingrowing hair) or (trichiasis) or (Wuchereria infestation) | Ingrowing hair | Wuchereria infestation | Trichiasis | Hair/hair follicle disease NOS | (Hair/hair follicle disease NOS) or (ingrowing hair) or (trichiasis) or (Wuchereria infestation) (disorder) | Entropion &/or trichiasis of eyelid | Trichiasis | Entropion and trichiasis of eyelid | Trichiasis - eyelid | Entropion &/or trichiasis of eyelid (disorder)
+BMGC_DS04214,BMG_DS006177,87065009,Dystrophia unguium,,,,,,,C0221260,,,,,Dystrophia unguium | Onychodystrophy | Nail dystrophy | Dystrophic nail | Dystrophia unguium (disorder)
+BMGC_DS04215,BMG_DS006178,14240001,Poliosis,,,,,,,C0221262,,MTHU014000,,,Poliosis | Poliosis (disorder)
+BMGC_DS04216,BMG_DS006182,238876005;49428008;201333007,Elastosis perforans serpiginosa,,EE70.Y,Other specified perforating dermatoses,L87.2,,,C0221271,C536202,MTHU015861;130100,MONDO:0007529,elastosis perforans serpiginosa,Elastosis perforans serpiginosa | Elastosis perforans serpiginosa (disorder) | Elastosis perforans serpiginosa | Elastosis perforans | Perforating elastosis | Elastosis perforans serpiginosa (disorder) | Perforating serpiginous elastosis | Miescher's elastoma | Keratosis follicularis serpiginosa | Perforating elastoma
+BMGC_DS04217,BMG_DS006184,389147003;35326002,Relative erythrocytosis,,,,,,,C0221276,,,,,Relative polycythemia (disorder) | Relative polycythaemia | Relative polycythemia | Spurious polycythaemia | Benign polycythaemia | Spurious polycythemia | Benign polycythemia | Relative erythrocytosis | Relative erythrocytosis | Relative polycythemia | Benign polycythemia | Spurious polycythemia | Benign polycythemia due to fall in plasma volume | Benign polycythaemia | Benign polycythaemia due to fall in plasma volume | Gaisbock's syndrome | Pseudo-polycythaemia | Relative polycythaemia | Relative erythrocytosis (disorder)
+BMGC_DS04218,BMG_DS006185,,,,,,,DOID:3448,penis Paget's disease,C0221286,,,MONDO:0002653,Paget disease of the penis,
+BMGC_DS04219,BMG_DS006187,5178002,"Synovioma, benign",,,,,DOID:2701,nodular tenosynovitis,C0221289,,,MONDO:0024715,benign synovial neoplasm,"Synovioma, benign | Synovioma, benign (morphologic abnormality) | Benign synovioma"
+BMGC_DS04220,BMG_DS006188,,,,,,,,,C0221290,,,MONDO:0018447,chondromyxoid fibroma,
+BMGC_DS04221,BMG_DS006190,400211001,Hereditary lymphedema and yellow nails,,,,,DOID:0050468,yellow nail syndrome,C0221348,,153300,MONDO:0007921,yellow nail syndrome,Hereditary lymphedema and yellow nails (disorder) | Hereditary lymphoedema and yellow nails | Hereditary lymphedema and yellow nails | Yellow nail syndrome
+BMGC_DS04222,BMG_DS006191,,,,,,,,,C0221355,,,MONDO:0016608,megalencephaly,
+BMGC_DS04223,BMG_DS006192,,,,,,,,,C0221357,,,MONDO:0021004,brachydactyly,
+BMGC_DS04224,BMG_DS006193,,,,,,,,,C0221363,,,MONDO:0000110,bifid nose,
+BMGC_DS04225,BMG_DS006204,,Non-Bacterial Thrombotic Endocarditis,"Endocarditis, Non-Infective",,,,DOID:0060068,nonbacterial thrombotic endocarditis,C0221390,D059905,,MONDO:0000610,marantic endocarditis,
+BMGC_DS04226,BMG_DS006206,,Atrophic Vaginitis,Atrophic Vaginitis,,,,,,C0221392,D059268,,,,
+BMGC_DS04227,BMG_DS006209,89476005,Pituitary cachexia,,5A61.0,Hypopituitarism,E23.0,DOID:0090072;DOID:0090087;DOID:0060875;DOID:0090073;DOID:0090076;DOID:0090092;DOID:0060873;DOID:0090080;DOID:0090075;DOID:0090077;DOID:0090071;DOID:0090082;DOID:0090084;DOID:0090074;DOID:0090093;DOID:0060874;DOID:0090078;DOID:0090070;DOID:0090085;DOID:0090094;DOID:0090086;DOID:0090083;DOID:0090081;DOID:0090079;DOID:0090089;DOID:0090090,hypogonadotropic hypogonadism 5 with or without anosmia | hypogonadotropic hypogonadism 7 with or without anosmia | hypogonadotropic hypogonadism 9 with or without anosmia | isolated growth hormone deficiency type IB | hypogonadotropic hypogonadism 21 with or without anosmia | hypogonadotropic hypogonadism 17 with or without anosmia | hypogonadotropic hypogonadism 6 with or without anosmia | isolated growth hormone deficiency type IA | isolated growth hormone deficiency type III | hypogonadotropic hypogonadism 10 with or without anosmia | hypogonadotropic hypogonadism 2 with or without anosmia | hypogonadotropic hypogonadism 22 with or without anosmia | hypogonadotropic hypogonadism 4 with or without anosmia | hypogonadotropic hypogonadism 1 with or without anosmia | hypogonadotropic hypogonadism 15 with or without anosmia | hypogonadotropic hypogonadism 16 with or without anosmia | hypogonadotropic hypogonadism 3 with or without anosmia | hypogonadotropic hypogonadism 14 with or without anosmia | hypogonadotropic hypogonadism 13 with or without anosmia | hypogonadotropic hypogonadism 19 with or without anosmia | hypogonadotropic hypogonadism 18 with or without anosmia | hypogonadotropic hypogonadism 12 with or without anosmia | hypogonadotropic hypogonadism | hypogonadotropic hypogonadism 11 with or without anosmia | hypogonadotropic hypogonadism 8 with or without anosmia | hypogonadotropic hypogonadism 20 with or without anosmia,C0221405,,,,,Pituitary cachexia | Pituitary cachexia (disorder)
+BMGC_DS04228,BMG_DS006210,190502001,Pituitary-dependent Cushing's disease,,5A70.0,Pituitarydependent Cushing disease,E24.0,DOID:3946,pituitary-dependent Cushing's disease,C0221406,,219090,MONDO:0009050,Cushing disease due to pituitary adenoma,Pituitary dependent hypercortisolism | Pituitary-dependent Cushing's disease | Cushing disease | Pituitary Cushing syndrome | Pituitary dependent Cushing disease | Cushing basophilism | Pituitary hyperadrenal corticism | Cushing's disease | Pituitary-dependent Cushing's disease (disorder)
+BMGC_DS04229,BMG_DS006213,68295002,Vitamin D-dependent rickets,,,,,DOID:0080883,vitamin D-dependent rickets,C0221468,,,MONDO:0024299,vitamin D-dependent rickets,Vitamin D-dependent rickets | Vitamin D-dependent rickets (disorder) | VDDR - vitamin D-dependent rickets
+BMGC_DS04230,BMG_DS006215,,alpha 1-Antitrypsin Deficiency,alpha 1-Antitrypsin Deficiency,,,,DOID:13372,alpha 1-antitrypsin deficiency,C0221757,D019896,613490,MONDO:0013282,alpha 1-antitrypsin deficiency,
+BMGC_DS04231,BMG_DS006216,,Brachial Plexus Neuritis,Brachial Plexus Neuritis,,,,DOID:3689,brachial plexus neuritis,C0221759,D020968,,MONDO:0006682,brachial plexus neuritis,
+BMGC_DS04232,BMG_DS006221,,,,,,,DOID:13195,nontoxic goiter,C0221777,,,MONDO:0001658,nontoxic goiter,
+BMGC_DS04233,BMG_DS006222,,,,,,,DOID:3767,vaginal discharge,C0227791,,,MONDO:0002770,vaginal discharge,
+BMGC_DS04234,BMG_DS006230,190590004;399959003,Premature aging syndrome,,,,,,,C0231341,,,MONDO:0019303,premature aging syndrome,Premature ageing syndrome | Adult premature ageing syndrome | Progeria syndrome | Adult premature aging syndrome | Premature aging syndrome | Progeria | Progeria (disorder) | Premature aging syndrome (disorder) | Premature ageing syndrome | Premature aging syndrome
+BMGC_DS04235,BMG_DS006270,155874000;32482005,Orthostatic proteinuria,,,,,DOID:9617,orthostatic proteinuria,C0232867,,,MONDO:0004838,orthostatic proteinuria,Orthostatic proteinuria | Orthostatic proteinuria (disorder) | Orthostatic proteinuria | Orthostatic albuminuria | Postural albuminuria | Benign postural proteinuria | Postural proteinuria | Orthostatic proteinuria (finding)
+BMGC_DS04236,BMG_DS006298,8913004,Primary physiologic amenorrhea,,,,,,,C0232939,,,,,Primary physiologic amenorrhea | Primary physiologic amenorrhoea | Primary physiologic amenorrhea (finding)
+BMGC_DS04237,BMG_DS006299,86030004,Secondary physiologic amenorrhea,,,,,,,C0232940,,,,,Secondary physiologic amenorrhea | Secondary physiologic amenorrhoea | Secondary physiologic amenorrhea (finding)
+BMGC_DS04238,BMG_DS006304,,,,,,,,,C0232981,,270960,MONDO:0010052,spermatogenic failure 4,
+BMGC_DS04239,BMG_DS006325,,,,,,,DOID:600,animal phobia,C0233711,,,MONDO:0003727,animal phobia,
+BMGC_DS04240,BMG_DS006327,,,,,,,DOID:5340,anterograde amnesia,C0233795,,,MONDO:0003398,anterograde amnesia,
+BMGC_DS04241,BMG_DS006342,,,,,,,,,C0234166,,,MONDO:0017658,hyperekplexia,
+BMGC_DS04242,BMG_DS006346,,"Neuralgia, Atypical",Neuralgia,,,,,,C0234247,D009437,,,,
+BMGC_DS04243,BMG_DS006347,,"Neuralgia, Stump",Neuralgia,,,,,,C0234249,D009437,,,,
+BMGC_DS04244,BMG_DS006355,,"Taste Disorder, Primary",Taste Disorders,,,,,,C0234297,D013651,,,,
+BMGC_DS04245,BMG_DS006356,,"Taste Disorder, Primary, Sweet",Taste Disorders,,,,,,C0234298,D013651,,,,
+BMGC_DS04246,BMG_DS006357,,"Taste Disorder, Primary, Salt",Taste Disorders,,,,,,C0234299,D013651,,,,
+BMGC_DS04247,BMG_DS006358,,"Taste Disorder, Primary, Bitter",Taste Disorders,,,,,,C0234300,D013651,,,,
+BMGC_DS04248,BMG_DS006360,,"Taste Disorder, Anterior Tongue",Taste Disorders,,,,,,C0234302,D013651,,,,
+BMGC_DS04249,BMG_DS006361,,"Taste Disorder, Secondary",Taste Disorders,,,,,,C0234303,D013651,,,,
+BMGC_DS04250,BMG_DS006362,,"Taste Disorder, Secondary, Sweet",Taste Disorders,,,,,,C0234304,D013651,,,,
+BMGC_DS04251,BMG_DS006363,,"Taste Disorder, Secondary, Salt",Taste Disorders,,,,,,C0234305,D013651,,,,
+BMGC_DS04252,BMG_DS006364,,"Taste Disorder, Secondary, Bitter",Taste Disorders,,,,,,C0234306,D013651,,,,
+BMGC_DS04253,BMG_DS006367,,"Taste Disorder, Posterior Tongue",Taste Disorders,,,,,,C0234319,D013651,,,,
+BMGC_DS04254,BMG_DS006370,,"Motor Disorder, Vagus Nerve",Vagus Nerve Diseases,,,,,,C0234329,D020421,,,,
+BMGC_DS04255,BMG_DS006371,,"Sensory Disorder, Vagus Nerve",Vagus Nerve Diseases,,,,,,C0234331,D020421,,,,
+BMGC_DS04256,BMG_DS006381,,,,,,,DOID:5691,visual cortex disease,C0234398,,,MONDO:0003584,visual cortex disorder,
+BMGC_DS04257,BMG_DS006395,,,,,,,DOID:4970,prosopagnosia,C0234512,,,MONDO:0003227,prosopagnosia,
+BMGC_DS04258,BMG_DS006396,,,,,,,DOID:4627,ideomotor apraxia,C0234523,,,MONDO:0006800,ideomotor apraxia,
+BMGC_DS04259,BMG_DS006397,,Generalized seizures,,,,,,,C0234533,,MTHU009234,,,
+BMGC_DS04260,BMG_DS006399,,Clonic Seizures,Seizures,,,,,,C0234535,D012640,,,,
+BMGC_DS04261,BMG_DS006419,,"Vertigo, Brain Stem",Vertigo,,,,,,C0234757,D014717,,,,
+BMGC_DS04262,BMG_DS006420,,,,,,,DOID:4399,acneiform dermatitis,C0234894,,,MONDO:0006521,acneiform dermatitis,
+BMGC_DS04263,BMG_DS006421,,Annular Erythema,,,,,,,C0234906,C562461,106500,MONDO:0007128,annular erythema,
+BMGC_DS04264,BMG_DS006426,,Simple Partial Seizures,"Epilepsies, Partial",,,,,,C0234974,D004828,,,,
+BMGC_DS04265,BMG_DS006427,267592003,Motor cortex epilepsy,,,,,,,C0234978,,,MONDO:0041284,primary motor cortex epilepsy,Primary motor cortex frontal lobe epilepsy (disorder) | Primary motor cortex frontal lobe epilepsy
+BMGC_DS04266,BMG_DS006429,95663000,Peripheral motor neuropathy,,,,,DOID:683,motor neuritis,C0235025,,MTHU041529,MONDO:0004004,motor nerve neuritis,Motor peripheral neuropathy | Motor neuritis | Peripheral motor neuropathy | Peripheral motor neuropathy (disorder)
+BMGC_DS04267,BMG_DS006430,,"Neuritis, Sensory",Neuritis,,,,,,C0235026,D009443,,,,
+BMGC_DS04268,BMG_DS006431,,,,,,,DOID:3602,toxic encephalopathy,C0235032,,,,,
+BMGC_DS04269,BMG_DS006435,68158006,Cycloplegia,,,,,DOID:10033,cycloplegia,C0235238,,,MONDO:0005555,cycloplegia,Cycloplegia | Paresis of accommodation | Visual accommodation paralysis | Paralysis of accommodation | Cycloplegic paralysis of accommodation | Cycloplegia (disorder) | Loss of accommodation | Ciliary muscle paresis | Accommodative paresis
+BMGC_DS04270,BMG_DS006436,,Keratopathy,,,,,DOID:2283,keratopathy,C0235270,,MTHU012241,MONDO:0002261,keratopathy,
+BMGC_DS04271,BMG_DS006445,86514004,Granulomatous hepatitis,,,,,DOID:2239,granulomatous hepatitis,C0235369,,MTHU074778,MONDO:0002252,granulomatous hepatitis,Granulomatous hepatitis | Granulomatous hepatitis (disorder)
+BMGC_DS04272,BMG_DS006447,45317003;213281004,Ketonemia,Ketosis,,,,,,C0235430,D007662,MTHU012717,,,Ketonemia | Ketonaemia | Ketonemia (disorder) | Ketonaemia | Ketonemia | Ketonemia (disorder)
+BMGC_DS04273,BMG_DS006451,195081002;282825002,Paroxysmal atrial fibrillation,,BC81.30,Paroxysmal atrial fibrillation,I48.0,,,C0235480,,MTHU046471,MONDO:1030011,paroxysmal atrial fibrillation,Paroxysmal atrial fibrillation | Paroxysmal atrial fibrillation (disorder) | AF - Paroxysmal atrial fibrillation | PAF - Paroxysmal atrial fibrillation | Intermittent atrial fibrillation | Paroxysmal atrial fibrillation | Paroxysmal atrial fibrillation (disorder)
+BMGC_DS04274,BMG_DS006453,,,,,,,,,C0235490,,,MONDO:0041114,peripheral ischemia,
+BMGC_DS04275,BMG_DS006458,,"Heart Failure, Right-Sided",Heart Failure,,,,,,C0235527,D006333,,,,
+BMGC_DS04276,BMG_DS006463,15170009,Submandibular lymphadenitis,,,,,DOID:4636,submandibular adenitis,C0235591,,,MONDO:0003066,submandibular adenitis,Submandibular lymphadenitis | Submandibular lymphadenitis (disorder) | Submandibular adenitis
+BMGC_DS04277,BMG_DS006464,127086001,Cervical lymphadenopathy,,,,,,,C0235592,,MTHU033335,,,Cervical lymphadenopathy | Cervical lymphadenopathy (disorder)
+BMGC_DS04278,BMG_DS006466,,,,,,,DOID:11125,qualitative platelet defect,C0235604,,,MONDO:0001197,qualitative platelet defect,
+BMGC_DS04279,BMG_DS006467,441815006,Proliferative glomerulonephritis,,,,,DOID:4778,proliferative glomerulonephritis,C0235618,,,MONDO:0003134,proliferative glomerulonephritis,Proliferative glomerulonephritis | Proliferative glomerulonephritis (disorder)
+BMGC_DS04280,BMG_DS006471,,,,,,,DOID:6933,bladder transitional cell papilloma,C0235754,,,MONDO:0004041,urothelial papilloma,
+BMGC_DS04281,BMG_DS006473,,,,,,,DOID:2145,malignant ovarian cyst,C0235770,,,MONDO:0002224,malignant ovarian cyst,
+BMGC_DS04282,BMG_DS006474,,,,,,,DOID:4948,gallbladder carcinoma,C0235782,,,MONDO:0003220,gallbladder carcinoma,
+BMGC_DS04283,BMG_DS006476,,,,,,,DOID:7756,neonatal leukemia,C0235813,,,MONDO:0004354,neonatal leukemia,
+BMGC_DS04284,BMG_DS006477,12301009,Neonatal urinary tract infection,,KA65.2,Neonatal urinary tract infection,P39.3,DOID:1375,neonatal urinary tract infectious disease,C0235815,,,MONDO:0001791,neonatal urinary tract infectious disease,Neonatal urinary tract infection | Neonatal urinary tract infection (disorder)
+BMGC_DS04285,BMG_DS006478,95628005,Neonatal encephalopathy,,,,P91.81,,,C0235820,,,,,Neonatal encephalopathy | Neonatal encephalopathy (disorder)
+BMGC_DS04286,BMG_DS006479,,,,,,,,,C0235833,,,MONDO:0005711,congenital diaphragmatic hernia,
+BMGC_DS04287,BMG_DS006481,206534003;268850004,Neonatal diarrhea,,,,,,,C0235840,,MTHU013422,,,(Neonatal diarrhea) or (neonatal chloridorrhea) | Neonatal chloridorrhea | Neonatal diarrhea | Neonatal chloridorrhoea | Neonatal diarrhoea | (Neonatal diarrhoea) or (neonatal chloridorrhoea) | (Neonatal diarrhoea) or (neonatal chloridorrhoea) (disorder) | Neonatal diarrhoea | Neonatal diarrhea | Neonatal diarrhea (disorder)
+BMGC_DS04288,BMG_DS006485,,,,,,,,,C0235864,,145700,MONDO:0016381,hypertrichosis lanuginosa congenita,
+BMGC_DS04289,BMG_DS006486,32595002,Mononeuritis,Mononeuropathies,,,,DOID:1802,mononeuritis,C0235880,D020422,,MONDO:0002121,mononeuritis simplex,Mononeuritis | Mononeuritis (disorder)
+BMGC_DS04290,BMG_DS006493,192824002;278849000,Cerebral atrophy,,,,,,,C0235946,,MTHU000199,,,Cerebral degeneration: [NOS] or [cerebral atrophy] | Cerebral degeneration NOS | Cerebral atrophy | Cerebral degeneration: [NOS] or [cerebral atrophy] (disorder) | Cerebral atrophy | Cerebral atrophy (disorder)
+BMGC_DS04291,BMG_DS006494,367102002;238124008,Zinc deficiency,,,,,,,C0235950,,MTHU056020,,,Zinc deficiency | Zinc deficiency (disorder)
+BMGC_DS04292,BMG_DS006495,5891000119102,Clostridium difficile diarrhea,,,,,,,C0235952,,,,,Clostridium difficile diarrhea | Clostridium difficile diarrhoea | Clostridium difficile diarrhea (disorder)
+BMGC_DS04293,BMG_DS006498,,,,,,,DOID:4905,pancreatic carcinoma,C0235974,,,MONDO:0005192,exocrine pancreatic carcinoma,
+BMGC_DS04294,BMG_DS006503,17231009;205792006,Fetal valproate syndrome,,,,,DOID:0060471,fetal valproate syndrome,C0236026,C536525,609442,MONDO:0012275,fetal valproate syndrome,Fetal valproate syndrome | Fetal valproate syndrome (disorder) | Foetal valproate spectrum disorder | Fetal valproate spectrum disorder | Fetal valproate syndrome | Fetal valproate syndrome (disorder)
+BMGC_DS04295,BMG_DS006505,95827002,Congenital hearing disorder,,,,,,,C0236038,,,,,Congenital hearing disorder | Congenital hearing disorder (disorder)
+BMGC_DS04296,BMG_DS006506,,"Polyposis, Gastric",,,,,,,C0236048,C562464,,MONDO:0008277,stomach polyp,
+BMGC_DS04297,BMG_DS006512,126765001,Gastrointestinal obstruction,,,,,,,C0236124,,MTHU023933,,,Gastrointestinal obstruction | Gastrointestinal obstruction (disorder)
+BMGC_DS04298,BMG_DS006514,,Pick Disease of the Brain,Pick Disease of the Brain,,,,DOID:11870,Pick's disease,C0236642,D020774,172700,MONDO:0008243,Pick disease,
+BMGC_DS04299,BMG_DS006516,268745002;154854002;191480000,Alcohol withdrawal syndrome,,,,,,,C0236663,,,MONDO:0005433,alcohol withdrawal,Other alcoholic psychoses | Korsakov psychosis | Alcohol withdrawal syndrome | Withdrawal syndrome - alcohol | Korsakov's psychosis | (Alcoholic psychosis: [Korsakov's] or [other]) or (withdrawal syndrome - alcohol) | (Alcoholic psychosis: [Korsakov's] or [other]) or (withdrawal syndrome - alcohol) (disorder) | Other alcoholic psychoses | Alcohol withdrawal syndrome | Korsakov psychosis | Withdrawal syndrome - alcohol | Korsakov's psychosis | (Alcoholic psychosis: [Korsakov's] or [other]) or (withdrawal syndrome - alcohol) | (Alcoholic psychosis: [Korsakov's] or [other]) or (withdrawal syndrome - alcohol) (disorder) | Alcohol withdrawal syndrome | Alcohol withdrawal syndrome (disorder) | Alcohol withdrawal
+BMGC_DS04300,BMG_DS006517,,Alcohol Related Disorders,Alcohol-Related Disorders,,,,,,C0236664,D019973,,MONDO:0021698,alcohol-related disorders,
+BMGC_DS04301,BMG_DS006519,,Cannabis-Related Disorder,Marijuana Abuse,,,,,,C0236735,D002189,,,,
+BMGC_DS04302,BMG_DS006520,,,,,,,DOID:14042,bipolar I disorder,C0236773,,,,,
+BMGC_DS04303,BMG_DS006521,,,,,,,DOID:3312,bipolar disorder,C0236780,,,,,
+BMGC_DS04304,BMG_DS006522,,,,,,,,,C0236788,,,MONDO:0000693,bipolar II disorder,
+BMGC_DS04305,BMG_DS006523,,,,,,,DOID:13487,childhood disintegrative disease,C0236791,,,MONDO:0015681,childhood disintegrative disorder,
+BMGC_DS04306,BMG_DS006524,,,,,,,DOID:0050432,Asperger syndrome,C0236792,,,MONDO:0005259,Asperger syndrome,
+BMGC_DS04307,BMG_DS006526,,,,,,,DOID:11037,dissociative amnesia,C0236795,,,MONDO:0001185,dissociative amnesia,
+BMGC_DS04308,BMG_DS006528,,,,,,,DOID:599,specific phobia,C0236801,,608251,MONDO:0012000,specific phobia,
+BMGC_DS04309,BMG_DS006531,,Chronobiology Disorders,Chronobiology Disorders,,,,,,C0236811,D021081,,,,
+BMGC_DS04310,BMG_DS006533,,,,,,,DOID:11385,expressive language disorder,C0236826,,,MONDO:0001276,expressive language disorder,
+BMGC_DS04311,BMG_DS006534,,,,,,,DOID:12685,mixed receptive-expressive language disorder,C0236827,,,MONDO:0001568,mixed receptive-expressive language disorder,
+BMGC_DS04312,BMG_DS006535,72820004,Neuroleptic-induced parkinsonism,,,,,,,C0236830,,,,,Neuroleptic-induced parkinsonism | Parkinsonism caused by neuroleptic drug (disorder) | Parkinsonism caused by neuroleptic drug
+BMGC_DS04313,BMG_DS006542,,,,,,,DOID:303,substance-related disorder,C0236969,,,MONDO:0002494,substance-related disorder,
+BMGC_DS04314,BMG_DS006543,,Alcohol-Induced Disorders,Alcohol-Induced Disorders,,,,,,C0236970,D020751,,MONDO:0021699,alcohol-induced disorders,
+BMGC_DS04315,BMG_DS006545,,,,,,,DOID:5117,dermoid cyst of ovary,C0237020,,166950,MONDO:0008167,dermoid cyst of ovary,
+BMGC_DS04316,BMG_DS006547,40845000,Gastrointestinal ulcer,,,,,,,C0237938,,,,,Gastrointestinal ulcer | Gastrointestinal ulcer (disorder)
+BMGC_DS04317,BMG_DS006551,965003,Toxic amblyopia,,,,,,,C0237979,,,MONDO:0041403,toxic amblyopia,Toxic amblyopia | Toxic amblyopia (disorder)
+BMGC_DS04318,BMG_DS006552,191171008;62403005,Glucose-6-phosphate dehydrogenase deficiency anemia,,,,,,,C0237987,,,,,Glucose-6-phosphate dehydrogenase deficiency anemia | Glucose-6-phosphate dehydrogenase deficiency anaemia | Glucose-6-phosphate dehydrogenase deficiency anemia (disorder) | Glucose-6-phosphate dehydrogenase deficiency anemia | G-6-PD deficiency anemia | Glucose-6-phosphate dehydrogenase deficiency | G6PD deficiency anemia | G-6-PD deficiency anaemia | G6PD deficiency anaemia | Glucose-6-phosphate dehydrogenase deficiency anaemia | Glucose-6-phosphate dehydrogenase deficiency anemia (disorder)
+BMGC_DS04319,BMG_DS006554,,,,,,,DOID:3608,appendix adenocarcinoma,C0238003,,,MONDO:0006087,appendix adenocarcinoma,
+BMGC_DS04320,BMG_DS006556,721798004,Invasive aspergillosis,,,,,,,C0238013,,,MONDO:0000240,invasive aspergillosis,Invasive aspergillosis (disorder) | Invasive aspergillosis
+BMGC_DS04321,BMG_DS006558,,Autonomic Dysreflexia,Autonomic Dysreflexia,,,,,,C0238015,D020211,,MONDO:0043975,autonomic dysreflexia,
+BMGC_DS04322,BMG_DS006559,,,,,,,DOID:6316,Bartholin's gland adenocarcinoma,C0238016,,,MONDO:0003853,Bartholin gland adenocarcinoma,
+BMGC_DS04323,BMG_DS006560,,,,,,,DOID:4682,extrahepatic bile duct carcinoma,C0238019,,,MONDO:0003090,extrahepatic bile duct carcinoma,
+BMGC_DS04324,BMG_DS006561,,"Botulism, Infantile",Botulism,,,,,,C0238027,D001906,,MONDO:0015804,infant botulism,
+BMGC_DS04325,BMG_DS006562,,,,,,,DOID:7497,brain ependymoma,C0238029,,,MONDO:0004245,ependymal tumor of brain,
+BMGC_DS04326,BMG_DS006563,,,,,,,DOID:3016,breast malignant phyllodes tumor,C0238031,,,MONDO:0021047,breast phyllodes tumor,
+BMGC_DS04327,BMG_DS006565,,,,,,,DOID:1626,breast duct papilloma,C0238034,,,MONDO:0021097,intraductal breast papilloma,
+BMGC_DS04328,BMG_DS006567,,Concentric hypertrophic cardiomyopathy,,,,,,,C0238044,,MTHU068797,,,
+BMGC_DS04329,BMG_DS006570,,Cerebral Angiitis,"Vasculitis, Central Nervous System",,,,,,C0238051,D020293,,,,
+BMGC_DS04330,BMG_DS006571,,"Xanthomatosis, Cerebrotendinous","Xanthomatosis, Cerebrotendinous",,,,DOID:4810,cerebrotendinous xanthomatosis,C0238052,D019294,213700,MONDO:0008948,cerebrotendinous xanthomatosis,
+BMGC_DS04331,BMG_DS006572,,"Chorea, Senile",Chorea,,,,,,C0238056,D002819,,,,
+BMGC_DS04332,BMG_DS006574,235828008,Chronic intestinal pseudo-obstruction,,,,,,,C0238062,,,MONDO:0017574,chronic intestinal pseudoobstruction,Chronic intestinal pseudo-obstruction | Chronic intestinal pseudo-obstruction (disorder)
+BMGC_DS04333,BMG_DS006575,,Secondary Biliary Cholangitis,"Liver Cirrhosis, Biliary",,,,,,C0238065,D008105,,,,
+BMGC_DS04334,BMG_DS006576,,"Colitis, Collagenous","Colitis, Collagenous",,,,DOID:0060183,collagenous colitis,C0238067,D046729,,MONDO:0000703,collagenous colitis,
+BMGC_DS04335,BMG_DS006578,,Cranial Epidural Abscess,Epidural Abscess,,,,,,C0238075,D020802,,,,
+BMGC_DS04336,BMG_DS006582,155976002;67667007,Acute endometritis,,,,,DOID:7528,acute endometritis,C0238103,,,MONDO:0004265,acute endometritis,Acute endometritis | Acute endometritis (disorder)
+BMGC_DS04337,BMG_DS006586,192984003;75036009;51603000;230418006,Lennox-Gastaut syndrome,,,,G40.81,,,C0238111,,606369;MTHU071842,MONDO:0016532,Lennox-Gastaut syndrome,Lennox-Gastaut syndrome | Lennox-Gastaut syndrome (disorder) | Cutis verticis gyrata | Cutis verticis gyrata (disorder)
+BMGC_DS04338,BMG_DS006590,190559001;267403002,Eunuchism,Eunuchism,,,,DOID:5003,eunuchism,C0238117,D005058,,MONDO:0005758,eunuchism,(Eunuchism) or (Kallman's syndrome) | Kallman's syndrome | Eunuchism | Kallmann's syndrome | Eunuchism | Eunuchism (disorder)
+BMGC_DS04339,BMG_DS006592,,,,,,,DOID:1963,fallopian tube carcinoma,C0238122,,,MONDO:0006206,fallopian tube carcinoma,
+BMGC_DS04340,BMG_DS006593,186428007;52486002,Necrotizing fasciitis,,1B71.Z,"Necrotising fasciitis, unspecified",M72.6,DOID:9602,necrotizing fasciitis,C0238124,,,MONDO:0004835,necrotizing fasciitis,Necrotizing fasciitis | Necrotising fasciitis | Necrotising fasciitis (disorder) | Necrotizing fasciitis | Necrotising fasciitis | Necrotizing fasciitis (disorder)
+BMGC_DS04341,BMG_DS006597,,,,,,,DOID:4779,focal embolic glomerulonephritis,C0238143,,,MONDO:0003135,focal embolic glomerulonephritis,
+BMGC_DS04342,BMG_DS006599,,,,,,,DOID:5262,heart sarcoma,C0238152,,,MONDO:0003354,heart sarcoma,
+BMGC_DS04343,BMG_DS006602,25065001,Hemoglobin E disease,,,,,DOID:5379,hemoglobin E disease,C0238159,,,MONDO:0016243,hemoglobin E disease,Hemoglobin E disease | Hemoglobin E-E disease | Haemoglobin E-E disease | Haemoglobin E disease | Homozygous for Hb E | Hemoglobin E disease (disorder)
+BMGC_DS04344,BMG_DS006608,,"Myositis, Inclusion Body","Myositis, Inclusion Body",,,,DOID:3429,inclusion body myositis,C0238190,D018979,147421,MONDO:0007827,inclusion body myositis,
+BMGC_DS04345,BMG_DS006609,,,,,,,DOID:4907,small intestine carcinoma,C0238196,,,MONDO:0005522,small intestine carcinoma,
+BMGC_DS04346,BMG_DS006610,,,,,,,DOID:1738,small intestine leiomyoma,C0238197,,,MONDO:0002092,small intestine leiomyoma,
+BMGC_DS04347,BMG_DS006611,,,,,,,DOID:9253,gastrointestinal stromal tumor,C0238198,,606764,MONDO:0011719,gastrointestinal stromal tumor,
+BMGC_DS04348,BMG_DS006612,,,,,,,DOID:5982,kidney fibrosarcoma,C0238208,,,MONDO:0003720,kidney fibrosarcoma,
+BMGC_DS04349,BMG_DS006616,,,,,,,DOID:271,hemangioma of liver,C0238246,,,MONDO:0002404,liver hemangioma,
+BMGC_DS04350,BMG_DS006618,234098006;400040008;77123007,Lymphedema praecox,,,,,DOID:0070213,hereditary lymphedema II,C0238261,,,,,Adolescent lymphedema | Infantile lymphedema (praecox) | Lymphedema praecox | Adolescent lymphoedema | Lymphoedema praecox | Infantile lymphoedema (praecox) | Adolescent lymphedema (disorder) | Hereditary lymphedema type II (disorder) | Hereditary lymphoedema type II | Hereditary lymphedema type II | Meige lymphoedema | Meige lymphedema | Meige disease | Lymphedema praecox | Lymphoedema praecox | Lymphedema praecox (disorder)
+BMGC_DS04351,BMG_DS006619,,Marchiafava-Bignami Disease,Marchiafava-Bignami Disease,,,,,,C0238265,D054319,,MONDO:0016370,Marchiafava-Bignami disease,
+BMGC_DS04352,BMG_DS006622,,Middle Cerebral Artery Syndrome,"Infarction, Middle Cerebral Artery",,,,,,C0238281,D020244,,,,
+BMGC_DS04353,BMG_DS006624,,Mucolipidosis Type IV,Mucolipidoses,,,,,,C0238286,D009081,252650,MONDO:0009653,mucolipidosis type IV,
+BMGC_DS04354,BMG_DS006625,,"Muscular Dystrophy, Facioscapulohumeral","Muscular Dystrophy, Facioscapulohumeral",,,,DOID:11727,facioscapulohumeral muscular dystrophy,C0238288,D020391,,MONDO:0001347,facioscapulohumeral muscular dystrophy,
+BMGC_DS04355,BMG_DS006626,190292006;21263006,Myxedema coma,,5A00.21,Myxoedema coma,E03.5,,,C0238298,,,,,Myxoedema coma | Myxedema coma | Myxoedema coma (disorder) | Myxedema coma | Myxoedema coma | Myxedema coma (disorder) | Hypothyroid coma
+BMGC_DS04356,BMG_DS006627,,,,,,,DOID:9261,nasopharynx carcinoma,C0238301,,,,,
+BMGC_DS04357,BMG_DS006630,129611009,Ischemic peripheral neuropathy,,,,,DOID:1195,ischemic neuropathy,C0238309,,,MONDO:0001408,ischemic neuropathy,Ischemic peripheral neuropathy | Ischaemic peripheral neuropathy | Ischemic peripheral neuropathy (disorder)
+BMGC_DS04358,BMG_DS006632,,,,,,,DOID:2156,ovarian germ cell cancer,C0238324,,603737,MONDO:0011366,ovarian germ cell tumor,
+BMGC_DS04359,BMG_DS006633,,,,,,,DOID:3444,scrotum Paget's disease,C0238330,,,MONDO:0002649,scrotum Paget disease,
+BMGC_DS04360,BMG_DS006635,,,,,,,DOID:4073,pancreatic cystadenocarcinoma,C0238337,,,MONDO:0002867,pancreatic cystadenocarcinoma,
+BMGC_DS04361,BMG_DS006636,68072000,Hereditary pancreatitis,,,,,,,C0238339,C537262,167800,MONDO:0008185,hereditary chronic pancreatitis,Hereditary pancreatitis | Hereditary pancreatitis (disorder)
+BMGC_DS04362,BMG_DS006638,,,,,,,DOID:5518,penis squamous cell carcinoma,C0238348,,,MONDO:0018352,squamous cell carcinoma of penis,
+BMGC_DS04363,BMG_DS006641,,,,,,,DOID:11838,penis sarcoma,C0238352,,,MONDO:0001387,penile sarcoma,
+BMGC_DS04364,BMG_DS006643,15973007;278513006;304737009,Hyperkalemic periodic paralysis,,,,,DOID:14451,hyperkalemic periodic paralysis,C0238357,,170500,MONDO:0008224,hyperkalemic periodic paralysis,Familial hyperkalemic periodic paralysis | Familial hyperkalaemic periodic paralysis | Familial hyperkalemic periodic paralysis (disorder) | Familial hyperkalaemic periodic paralysis | Myotonic periodic paralysis | Adynamia episodica hereditaria | Gamstorp disease | Hyperkalaemic periodic paralysis | Familial hyperkalemic periodic paralysis | Hyperkalemic periodic paralysis | Hyperkalemic periodic paralysis (disorder) | Periodic paralysis II | Familial hyperkalemic periodic paralysis (disorder) | Familial hyperkalemic periodic paralysis | Hyperkalemic periodic paralysis | Familial hyperkalaemic periodic paralysis | Adynamia episodica hereditaria | Gamstorp disease | Hyperkalaemic periodic paralysis
+BMGC_DS04365,BMG_DS006644,240093008;82732003,Hypokalemic periodic paralysis,,,,,DOID:14452,hypokalemic periodic paralysis,C0238358,,,MONDO:0008223,hypokalemic periodic paralysis,Familial hypokalaemic periodic paralysis | Familial hypokalemic periodic paralysis | Hypokalemic periodic paralysis | Hypokalaemic periodic paralysis | Hypokalemic periodic paralysis (disorder) | Familial hypokalemic periodic paralysis | Hypokalemic periodic paralysis | Hypokalaemic periodic paralysis | Periodic paralysis I | Familial hypokalaemic periodic paralysis | Familial hypokalemic periodic paralysis (disorder) | HOKPP - hypokalemic periodic paralysis | HOKPP - hypokalaemic periodic paralysis
+BMGC_DS04366,BMG_DS006650,73144008,Pneumoconiosis caused by talc,,,,,DOID:10329,pulmonary talcosis,C0238377,,,MONDO:0001003,pneumoconiosis due to talc,Talcosis | Pulmonary talcosis | Talc lung disease | Talc pneumoconiosis | Talc workers' pneumoconiosis | Pneumoconiosis caused by talc (disorder) | Pneumoconiosis caused by talc
+BMGC_DS04367,BMG_DS006651,8549006,Desquamative interstitial pneumonia,,,,J84.117,DOID:0050158,desquamative interstitial pneumonia,C0238378,,263000,MONDO:0009887,desquamative interstitial pneumonia,Desquamative interstitial pneumonia | Desquamative interstitial pneumonitis | Desquamative interstitial pneumonitis (disorder)
+BMGC_DS04368,BMG_DS006652,,,,,,,DOID:4054,prostate sarcoma,C0238393,,,MONDO:0002854,prostate sarcoma,
+BMGC_DS04369,BMG_DS006653,190939007,Pycnodysostosis,Pycnodysostosis,,,,DOID:0080038,pycnodysostosis,C0238402,D058631,265800,MONDO:0009940,pycnodysostosis,Pycnodysostosis | Pycnodysostosis (disorder)
+BMGC_DS04370,BMG_DS006655,,,,,,,DOID:5534,renal pelvis squamous cell carcinoma,C0238409,,,MONDO:0003497,renal pelvis squamous cell carcinoma,
+BMGC_DS04371,BMG_DS006659,83920001,Selenium deficiency,,,,,,,C0238421,,,,,Selenium deficiency | Selenium deficiency (disorder)
+BMGC_DS04372,BMG_DS006660,417425009,Hemoglobin SS disease with crisis,,,,,,,C0238425,,,,,Hemoglobin SS disease with crisis (disorder) | Hemoglobin SS disease with crisis | Haemoglobin SS disease with crisis | Sickle cell crisis | Sickle cell anemia with crisis | Sickle cell anaemia with crisis
+BMGC_DS04373,BMG_DS006661,,,,,,,DOID:5503,spinal cord ependymoma,C0238432,,,MONDO:0003473,spinal cord ependymoma,
+BMGC_DS04374,BMG_DS006662,,"Epidural Abscess, Spinal",Epidural Abscess,,,,,,C0238434,D020802,,,,
+BMGC_DS04375,BMG_DS006667,,,,,,,DOID:5680,embryonal testis carcinoma,C0238448,,,MONDO:0006446,testicular embryonal carcinoma,
+BMGC_DS04376,BMG_DS006668,,,,,,,DOID:5551,choriocarcinoma of the testis,C0238449,,,MONDO:0003508,choriocarcinoma of testis,
+BMGC_DS04377,BMG_DS006670,,Cavernous Sinus Thrombosis,Cavernous Sinus Thrombosis,,,,DOID:3575,cavernous sinus thrombosis,C0238454,D020226,,MONDO:0002694,cavernous sinus thrombosis,
+BMGC_DS04378,BMG_DS006672,,,,,,,,,C0238461,,,MONDO:0006468,thyroid gland undifferentiated (anaplastic) carcinoma,
+BMGC_DS04379,BMG_DS006673,,,,,,,DOID:3973,medullary thyroid carcinoma,C0238462,,,MONDO:0015277,medullary thyroid gland carcinoma,
+BMGC_DS04380,BMG_DS006674,,,,,,,DOID:3969,papillary thyroid carcinoma,C0238463,,,MONDO:0005075,thyroid gland papillary carcinoma,
+BMGC_DS04381,BMG_DS006677,234375006,Transient erythroblastopenia of childhood,,,,,,,C0238478,C536980,227050,MONDO:0009197,transient erythroblastopenia of childhood,Transient erythroblastopenia of childhood | TEC - Transient erythroblastopenia of childhood | Transient erythroblastopenia of childhood (disorder)
+BMGC_DS04382,BMG_DS006678,12068006,Prolapse of urethra,,,,,DOID:12369,prolapse of urethra,C0238502,,,MONDO:0001514,prolapse of urethra,Prolapse of urethra | Urethrocele | Prolapse of urethra (disorder) | Urethrocoele
+BMGC_DS04383,BMG_DS006679,,,,,,,,,C0238506,,,MONDO:0019640,posterior urethral valve,
+BMGC_DS04384,BMG_DS006681,,,,,,,DOID:1901,vagina sarcoma,C0238519,,,MONDO:0002140,vagina sarcoma,
+BMGC_DS04385,BMG_DS006682,,,,,,,DOID:2096,vulvar sarcoma,C0238525,,,MONDO:0005214,vulva sarcoma,
+BMGC_DS04386,BMG_DS006683,80960004,Infection by Yersinia enterocolitica,,,,,,,C0238528,,,,,Infection by Yersinia enterocolitica | Infection caused by Yersinia enterocolitica | Infection caused by Yersinia enterocolitica (disorder)
+BMGC_DS04387,BMG_DS006684,238872007,Acrogeria,,,,,,,C0238590,,MTHU070473,,,Acrogeria | Gottron's syndrome | Acrogeria (disorder)
+BMGC_DS04388,BMG_DS006685,275781001;167535000;35912001,Aminoaciduria,,,,,,,C0238621,,MTHU000661,,,"Aminoaciduria | Aminoaciduria (finding) | (Urine amino acids) or (aminoaciduria) | Amino-acids, urine | Aminoaciduria | Urine amino acids | (Urine amino acids) or (aminoaciduria) (procedure) | Aminoaciduria | Aminoaciduria (disorder)"
+BMGC_DS04389,BMG_DS006689,,,,,,,DOID:5393,brain angioma,C0238814,,,MONDO:0003428,brain hemangioma,
+BMGC_DS04390,BMG_DS006695,231870008,Conjunctival telangiectasis,,,,,,,C0239105,,,,,Conjunctival telangiectasis | Conjunctival telangiectasis (disorder)
+BMGC_DS04391,BMG_DS006697,20639004,Candidiasis of the esophagus,,,,,DOID:13146,esophageal candidiasis,C0239295,,,MONDO:0001648,esophageal candidiasis,Candidiasis of the esophagus | Candidiasis of the oesophagus | Candidiasis of the esophagus (disorder) | Candidiasis of oesophagus | Oesophageal thrush | Candidosis of oesophagus | Esophageal thrush | Candidosis of esophagus | Candidiasis of esophagus | Candida of esophagus
+BMGC_DS04392,BMG_DS006705,,"Color Blindness, Green",Color Vision Defects,,,,,,C0239777,D003117,,,,
+BMGC_DS04393,BMG_DS006708,,Harlequin Fetus,"Ichthyosis, Lamellar",,,,,,C0239849,D017490,,,,
+BMGC_DS04394,BMG_DS006709,,"Fibrosis, Liver",Liver Cirrhosis,,,,,,C0239946,D008103,,,,
+BMGC_DS04395,BMG_DS006710,119247004,Hypoalbuminemia,Hypoalbuminemia,,,,,,C0239981,D034141,MTHU000014,,,Hypoalbuminemia | Hypoalbuminaemia | Serum albumin low | Hypoalbuminemia (disorder)
+BMGC_DS04396,BMG_DS006711,,,,,,,,,C0240063,,,MONDO:0020356,coloboma of iris,
+BMGC_DS04397,BMG_DS006714,,,,,,,DOID:10071,larynx squamous papilloma,C0240164,,,MONDO:0000935,larynx squamous papilloma,
+BMGC_DS04398,BMG_DS006718,,Rotary Nystagmus,"Nystagmus, Pathologic",,,,,,C0240595,D009759,,,,
+BMGC_DS04399,BMG_DS006723,,,,,,,DOID:5815,cerebral lymphoma,C0240803,,,MONDO:0003655,cerebral lymphoma,
+BMGC_DS04400,BMG_DS006725,,Rheumatoid Vasculitis,Rheumatoid Vasculitis,,,,,,C0240903,D056653,,MONDO:0043267,rheumatoid vasculitis,
+BMGC_DS04401,BMG_DS006726,,,,,,,DOID:0111568,congenital vertical talus,C0240912,,192950,MONDO:0008652,congenital vertical talus,
+BMGC_DS04402,BMG_DS006727,,,,,,,,,C0240991,,,MONDO:0100311,sensory ataxia,
+BMGC_DS04403,BMG_DS006728,,,,,,,,,C0241005,,123320,MONDO:0007402,"creatine phosphokinase, elevated serum",
+BMGC_DS04404,BMG_DS006730,93448009,Superficial ulcer of skin (disorder),,,,,,,C0241069,,,,,Superficial ulcer of skin | Erosion of skin | Superficial ulcer of skin (disorder)
+BMGC_DS04405,BMG_DS006737,,,,,,,DOID:13812,adhesions of uterus,C0241593,,,MONDO:0001809,adhesions of uterus,
+BMGC_DS04406,BMG_DS006744,,Cerebrovascular Insufficiency,Cerebrovascular Disorders,,,,,,C0241832,D002561,,,,
+BMGC_DS04407,BMG_DS006750,,"Hematuria, Benign Familial",,,,,,,C0241908,C562476,,MONDO:0957317,"hematuria, benign familial",
+BMGC_DS04408,BMG_DS006751,,Autoimmune Chronic Hepatitis,"Hepatitis, Autoimmune",,,,DOID:2048,autoimmune hepatitis,C0241910,D019693,,,,
+BMGC_DS04409,BMG_DS006755,234416002,X-linked hypogammaglobulinemia,,,,,,,C0241932,,,,,X-linked hypogammaglobulinaemia | X-linked hypogammaglobulinemia | X-linked hypogammaglobulinemia (disorder)
+BMGC_DS04410,BMG_DS006758,,,,,,,DOID:8411,kidney angiomyolipoma,C0241961,,,MONDO:0004555,kidney angiomyolipoma,
+BMGC_DS04411,BMG_DS006762,,,,,,,DOID:2093,vulvar melanoma,C0241989,,,MONDO:0002205,vulvar melanoma,
+BMGC_DS04412,BMG_DS006765,,Sciatic Neuritis,Sciatic Neuropathy,,,,,,C0242013,D020426,,,,
+BMGC_DS04413,BMG_DS006766,,"Pancreatitis, Acute Edematous",Pancreatitis,,,,,,C0242032,D010195,,,,
+BMGC_DS04414,BMG_DS006770,196118009;67599009,Pulmonary congestion,,,,,,,C0242073,,,,,Pulmonary congestion | Pulmonary congestion (disorder)
+BMGC_DS04415,BMG_DS006773,,Thrombotic Stroke,Thrombotic Stroke,,,,,,C0242129,D000083244,,,,
+BMGC_DS04416,BMG_DS006778,,Pelvic Inflammatory Disease,Pelvic Inflammatory Disease,,,,DOID:1003,pelvic inflammatory disease,C0242172,D000292,,MONDO:0000922,pelvic inflammatory disease,
+BMGC_DS04417,BMG_DS006779,,"Jaundice, Hemolytic",Jaundice,,,,,,C0242183,D007565,,,,
+BMGC_DS04418,BMG_DS006781,,Calcium Pyrophosphate Dihydrate Deposition,Chondrocalcinosis,,,,,,C0242217,D002805,,,,
+BMGC_DS04419,BMG_DS006782,193683001;155143000;53481002,Color blindness,,9D44,Impairment of colour vision,H53.5,DOID:13399,color blindness,C0242225,,,,,No colour perception | Colour blindness | Color blindness | No color perception | Color blindness (disorder) | Color blindness | Colour blindness | Colour blindness (disorder) | Color vision deficiency | Colour vision deficiency | Color vision deficiency (disorder)
+BMGC_DS04420,BMG_DS006783,,Coronary Stenosis,Coronary Stenosis,,,,DOID:4248,coronary stenosis,C0242231,D023921,,MONDO:0006715,coronary stenosis,
+BMGC_DS04421,BMG_DS006785,,McCune-Albright Syndrome,"Fibrous Dysplasia, Polyostotic",,,,,,C0242292,D005359,174800,MONDO:0018919,McCune-Albright syndrome,
+BMGC_DS04422,BMG_DS006786,,,,,,,DOID:0060125,heavy chain disease,C0242310,,,MONDO:0015044,mu-heavy chain disease,
+BMGC_DS04423,BMG_DS006789,,Dyslipidemias,Dyslipidemias,,,,,,C0242339,D050171,,,,
+BMGC_DS04424,BMG_DS006790,,Sexual Infantilism,Sexual Infantilism,,,,,,C0242341,D050035,,,,
+BMGC_DS04425,BMG_DS006791,,Sheehan Syndrome,Hypopituitarism,,,,DOID:9476,Sheehan syndrome,C0242342,D007018,,MONDO:0019618,Sheehan syndrome,
+BMGC_DS04426,BMG_DS006792,154700009;190469009;267481002;32390006,Panhypopituitarism,,5A61.0,Hypopituitarism,E23.0,DOID:0090072;DOID:0090087;DOID:0060875;DOID:0090073;DOID:0090076;DOID:0090092;DOID:0060873;DOID:0090080;DOID:0090075;DOID:0090077;DOID:0090071;DOID:0090082;DOID:0090084;DOID:0090074;DOID:0090093;DOID:0060874;DOID:0090078;DOID:0090070;DOID:0090085;DOID:0090094;DOID:0090086;DOID:0090083;DOID:9410;DOID:0090081;DOID:0090079;DOID:0090089;DOID:0090090,hypogonadotropic hypogonadism 5 with or without anosmia | hypogonadotropic hypogonadism 7 with or without anosmia | hypogonadotropic hypogonadism 9 with or without anosmia | isolated growth hormone deficiency type IB | hypogonadotropic hypogonadism 21 with or without anosmia | hypogonadotropic hypogonadism 17 with or without anosmia | hypogonadotropic hypogonadism 6 with or without anosmia | isolated growth hormone deficiency type IA | isolated growth hormone deficiency type III | hypogonadotropic hypogonadism 10 with or without anosmia | hypogonadotropic hypogonadism 2 with or without anosmia | hypogonadotropic hypogonadism 22 with or without anosmia | hypogonadotropic hypogonadism 4 with or without anosmia | hypogonadotropic hypogonadism 1 with or without anosmia | hypogonadotropic hypogonadism 15 with or without anosmia | hypogonadotropic hypogonadism 16 with or without anosmia | hypogonadotropic hypogonadism 3 with or without anosmia | hypogonadotropic hypogonadism 14 with or without anosmia | hypogonadotropic hypogonadism 13 with or without anosmia | hypogonadotropic hypogonadism 19 with or without anosmia | hypogonadotropic hypogonadism 18 with or without anosmia | hypogonadotropic hypogonadism 12 with or without anosmia | hypogonadotropic hypogonadism | hypogonadotropic hypogonadism 11 with or without anosmia | combined pituitary hormone deficiency | hypogonadotropic hypogonadism 8 with or without anosmia | hypogonadotropic hypogonadism 20 with or without anosmia,C0242343,C580003,MTHU017686,MONDO:0019591,panhypopituitarism,Hypopituit (& [panhypopituitarism]) | Hypopituit/panhypopituitarism | Panhypopituitarism | Hypopituit (& [panhypopituitarism]) (disorder) | Hypopituitarism: [NOS] or [Sheehan's syndrome] or [Simmond's disease] or [Panhypopituitarism] | Sheehan's syndrome | Panhypopituitarism | Hypopituitarism NOS | Simmond's disease | Hypopituitarism: [NOS] or [Sheehan's syndrome] or [Simmond's disease] or [Panhypopituitarism] (disorder) | Panhypopituitarism | Hypopituit/panhypopituitarism | Hypopituit (& [panhypopituitarism]) | Hypopituit (& [panhypopituitarism]) (disorder) | Panhypopituitarism | Primary hypopituitarism | Simmonds' disease | Deficient secretion of all pituitary hormones | Simmond's disease | Panhypopituitarism (disorder)
+BMGC_DS04427,BMG_DS006793,860914002;398175007;397803000;33967003,Erectile dysfunction,,,,,,,C0242350,,MTHU026591,MONDO:0005362,erectile dysfunction,Erectile dysfunction | Failure of erection | Erectile dysfunction (disorder) | Male erectile disorder | Male erectile disorder (disorder) | Male erectile disorder | Erectile dysfunction | Impotence (disorder) | Impotence | Failure of erection | Sexual impotence | Erectile dysfunction | Male erectile disorder | Impotence | Failure of erection | Erectile dysfunction | Male erectile disorder (disorder)
+BMGC_DS04428,BMG_DS006794,,Congenital Disorders,"Congenital, Hereditary, and Neonatal Diseases and Abnormalities",,,,,,C0242354,D009358,,,,
+BMGC_DS04429,BMG_DS006795,,,,,,,DOID:1799,islet cell tumor,C0242363,,,,,
+BMGC_DS04430,BMG_DS006796,,,,,,,,,C0242379,,211980,MONDO:0008903,lung cancer,
+BMGC_DS04431,BMG_DS006797,,Libman-Sacks Disease,"Lupus Erythematosus, Systemic",,,,,,C0242380,D008180,,MONDO:0850223,Libman-Sacks endocarditis,
+BMGC_DS04432,BMG_DS006798,,Lyme Arthritis,Lyme Disease,,,,,,C0242381,D008193,,,,
+BMGC_DS04433,BMG_DS006799,18222007;267718000,Age related macular degeneration,,,,,DOID:10871,age related macular degeneration,C0242383,,,MONDO:0005150,age-related macular degeneration,Age related macular degeneration | Age related macular degeneration (disorder) | Age related macular degeneration | Age-related macular degeneration | ARMD - Age-related macular degeneration | Senile macular retinal degeneration | SMD - Senile macular degeneration | AMD - Age-related macular degeneration | Senile macular degeneration | Age-related macular degeneration (disorder) | AAMD - Age related macular degeneration
+BMGC_DS04434,BMG_DS006800,,Mandibulofacial Dysostosis,Mandibulofacial Dysostosis,,,,DOID:2908,Treacher Collins syndrome,C0242387,D008342,,MONDO:0015483;MONDO:0002457,Treacher-Collins syndrome | mandibulofacial dysostosis,
+BMGC_DS04435,BMG_DS006803,,,,,,,DOID:6929;DOID:10175,retinal edema | optic papillitis,C0242420,,,MONDO:0004037,retinal edema,
+BMGC_DS04436,BMG_DS006804,,Parkinsonian Disorders,Parkinsonian Disorders,,,,,,C0242422,D020734,,MONDO:0021095,parkinsonian disorder,
+BMGC_DS04437,BMG_DS006805,,Ramsay Hunt Paralysis Syndrome,Parkinsonian Disorders,,,,,,C0242423,D020734,,,,
+BMGC_DS04438,BMG_DS006806,233890005,Chylopericardium,Pericardial Effusion,,,I31.39,,,C0242426,D010490,,,,Chylopericardium | Chylopericardium (disorder)
+BMGC_DS04439,BMG_DS006807,,Simple Pulmonary Eosinophilia,Pulmonary Eosinophilia,,,,DOID:9503,Loeffler syndrome,C0242459,D011657,,,,
+BMGC_DS04440,BMG_DS006808,,"Purpura, Nonthrombocytopenic",IgA Vasculitis,,,,,,C0242461,D011695,,,,
+BMGC_DS04441,BMG_DS006809,278525009;23680005,Enthesopathy,Enthesopathy,,,,DOID:204,enthesopathy,C0242490,D000070676,,MONDO:0002183,enthesopathy,Enthesopathy | Enthesopathy (disorder)
+BMGC_DS04442,BMG_DS006811,,Paroxysmal Reciprocal Tachycardia,"Tachycardia, Paroxysmal",,,,,,C0242513,D013614,,,,
+BMGC_DS04443,BMG_DS006813,,"Gonadal Dysgenesis, 45,X",Turner Syndrome,,,,,,C0242526,D014424,,MONDO:0020466,monosomy X,
+BMGC_DS04444,BMG_DS006814,445009001,Azotemia,Azotemia,,,,,,C0242528,D053099,MTHU013356,,,Azotemia (disorder) | Azotaemia | Azotemia
+BMGC_DS04445,BMG_DS006817,194177006;73519005,Opsoclonus,Ocular Motility Disorders,,,,,,C0242567,D015835,MTHU010637,,,Opsoclonia | Opsoclonus | Opsoclonia (finding) | Opsoclonus | Opsoclonia | Opsoclonus (finding)
+BMGC_DS04446,BMG_DS006818,,Bare Lymphocyte Syndrome,Severe Combined Immunodeficiency,,,,DOID:5812,MHC class II deficiency,C0242583,D016511,,,,
+BMGC_DS04447,BMG_DS006819,128091003;13172003;275758003,Autoimmune thrombocytopenia,,,,,,,C0242584,,MTHU004966,MONDO:0019098,autoimmune thrombocytopenia,Autoimmune thrombocytopenia | Autoimmune thrombocytopenia (disorder) | Primary ITP (immune thrombocytopenia) | Chronic idiopathic thrombocytopenic purpura | Werlhof's disease | Purpura hemorrhagica | Chronic thrombocytopenic purpura | Autoimmune thrombocytopenic purpura | Purpura haemorrhagica | Chronic idiopathic thrombocytopenic purpura (disorder) | Autoimmune thrombocytopenia | Autoimmune thrombocytopenia (disorder)
+BMGC_DS04448,BMG_DS006820,,Leukocyte-Adhesion Deficiency Syndrome,Leukocyte-Adhesion Deficiency Syndrome,,,,DOID:6612,leukocyte adhesion deficiency,C0242597,D018370,,,,
+BMGC_DS04449,BMG_DS006823,,Brown-Sequard Syndrome,Brown-Sequard Syndrome,,,,DOID:606,Brown-Sequard syndrome,C0242644,D018437,,MONDO:0003754,Brown-Sequard syndrome,
+BMGC_DS04450,BMG_DS006824,,Blue Toe Syndrome,Blue Toe Syndrome,,,,DOID:14121,blue toe syndrome,C0242645,D018438,,MONDO:0001883,blue toe syndrome,
+BMGC_DS04451,BMG_DS006825,,,,,,,,,C0242647,,137245,MONDO:0007650,MALT lymphoma,
+BMGC_DS04452,BMG_DS006826,,Protein S Deficiency,Protein S Deficiency,,,,DOID:2451,protein S deficiency,C0242666,D018455,,MONDO:0002304,protein S deficiency,
+BMGC_DS04453,BMG_DS006830,,"Bone Demineralization, Pathologic","Bone Demineralization, Pathologic",,,,,,C0242699,D018488,,,,
+BMGC_DS04454,BMG_DS006831,,Space Motion Sickness,Space Motion Sickness,,,,DOID:4796,space motion sickness,C0242700,D018489,,MONDO:0003147,space motion sickness,
+BMGC_DS04455,BMG_DS006833,,Bronchiolitis Obliterans Organizing Pneumonia,Cryptogenic Organizing Pneumonia,,,,DOID:0050157,cryptogenic organizing pneumonia,C0242770,D018549,,MONDO:0015264,cryptogenic organizing pneumonia,
+BMGC_DS04456,BMG_DS006834,,,,,,,DOID:1614,male breast cancer,C0242788,,,,,
+BMGC_DS04457,BMG_DS006836,232016005,Proliferative vitreoretinopathy,,,,,DOID:9719,neovascular inflammatory vitreoretinopathy,C0242852,,MTHU059298,MONDO:0700115,proliferative vitreoretinopathy,Proliferative vitreoretinopathy | PVR - Proliferative vitreoretinopathy | Fibrosis of retina | Retinitis proliferans | Proliferative vitreoretinopathy (disorder)
+BMGC_DS04458,BMG_DS006837,204342004;52670000,Congenital atresia of pulmonary valve,,,,,,,C0242855,,,,,Congenital atresia of pulmonary valve | Congenital atresia of pulmonary valve (disorder) | Imperforate pulmonary valve | Congenital atresia of pulmonary valve | Congenital atresia of pulmonary valve (disorder)
+BMGC_DS04459,BMG_DS006841,,Systemic Inflammatory Response Syndrome,Systemic Inflammatory Response Syndrome,,,,,,C0242966,D018746,,,,
+BMGC_DS04460,BMG_DS006842,,Multiple Chemical Sensitivity,Multiple Chemical Sensitivity,,,,DOID:4661,multiple chemical sensitivity,C0242992,D018777,,MONDO:0005862,obsolete multiple chemical sensitivity,
+BMGC_DS04461,BMG_DS006848,,Abdominal Abscess,Abdominal Abscess,,,,,,C0243001,D018784,,,,
+BMGC_DS04462,BMG_DS006849,,,,,,,,,C0243002,,605067,MONDO:0011514,tricuspid atresia,
+BMGC_DS04463,BMG_DS006850,,Viral Encephalitis,"Encephalitis, Viral",,,,,,C0243010,D018792,,MONDO:0006009,viral encephalitis,
+BMGC_DS04464,BMG_DS006851,,Hantavirus Pulmonary Syndrome,Hantavirus Pulmonary Syndrome,,,,DOID:14472,hantavirus pulmonary syndrome,C0243025,D018804,,MONDO:0017879,hantavirus pulmonary syndrome,
+BMGC_DS04465,BMG_DS006852,91302008;186392004,Sepsis,Sepsis,,,,,,C0243026,D018805,MTHU055817,,,Systemic infection | Sepsis | Sepsis (disorder) | (Septicaemia NOS) or (sepsis) | Sepsis | (Septicemia NOS) or (sepsis) | Septicaemia NOS | Septicemia NOS | (Septicaemia NOS) or (sepsis) (disorder)
+BMGC_DS04466,BMG_DS006855,277879009,Autonomic neuropathy,,,,,DOID:11504,autonomic neuropathy,C0259749,,MTHU052930,MONDO:0001300,autonomic neuropathy,Autonomic neuropathy | Autonomic neuropathy (disorder)
+BMGC_DS04467,BMG_DS006857,,,,,,,,,C0259771,,184500,MONDO:0008485,sebocystomatosis,
+BMGC_DS04468,BMG_DS006860,,,,,,,,,C0259779,,,MONDO:0000845,fibrous dysplasia,
+BMGC_DS04469,BMG_DS006861,,,,,,,DOID:6951,telangiectatic osteogenic sarcoma,C0259782,,,MONDO:0004050,telangiectatic osteogenic sarcoma,
+BMGC_DS04470,BMG_DS006862,,,,,,,DOID:5076,mixed glioma,C0259783,,,MONDO:0003268,mixed glioma,
+BMGC_DS04471,BMG_DS006864,,,,,,,DOID:5058,rhabdoid meningioma,C0259786,,,MONDO:0003262,rhabdoid meningioma,
+BMGC_DS04472,BMG_DS006866,193767008;42513006,Punctate keratitis,,,,H16.14,DOID:12197,punctate epithelial keratoconjunctivitis,C0259799,,MTHU037418,,,(Punctate keratitis [& Thygeson's superficial] ) or (keratitic precipitates) | Thygeson's superficial punctate keratitis | Keratitic precipitates | Punctate keratitis | (Punctate keratitis [& Thygeson's superficial] ) or (keratitic precipitates) (disorder) | Punctate keratitis | Superficial punctate keratitis | Punctate keratitis (disorder) | PK - Punctate keratitis | Punctate epithelial keratitis
+BMGC_DS04473,BMG_DS006867,41720003,Purulent endophthalmitis,,9C20.2,Purulent endophthalmitis,H44.0,DOID:9724,purulent endophthalmitis,C0259800,,,MONDO:0004863,purulent endophthalmitis,Purulent endophthalmitis | Purulent endophthalmitis (disorder)
+BMGC_DS04474,BMG_DS006870,,,,,,,,,C0260662,,,MONDO:0021945,hearing disorder,
+BMGC_DS04475,BMG_DS006874,,,,,,,DOID:4932,ampulla of Vater carcinoma,C0262401,,,MONDO:0017590,carcinoma of the ampulla of vater,
+BMGC_DS04476,BMG_DS006879,,"Cardiac valvular dysplasia, X-linked",,,,,,,C0262436,C535576,314400,MONDO:0010753,"cardiac valvular dysplasia, X-linked",
+BMGC_DS04477,BMG_DS006887,,Anterolateral Myocardial Infarction,Anterior Wall Myocardial Infarction,,,,DOID:5845,anterolateral myocardial infarction,C0262564,D056988,,MONDO:0006652,anterolateral myocardial infarction,
+BMGC_DS04478,BMG_DS006888,,Anteroseptal Myocardial Infarction,Anterior Wall Myocardial Infarction,,,,DOID:5855,anteroseptal myocardial infarction,C0262565,D056988,,MONDO:0003679,anteroseptal myocardial infarction,
+BMGC_DS04479,BMG_DS006891,,,,,,,DOID:5411,lung oat cell carcinoma,C0262584,,,,,
+BMGC_DS04480,BMG_DS006894,,,,,,,DOID:7608,parathyroid adenoma,C0262587,,,MONDO:0006890,parathyroid gland adenoma,
+BMGC_DS04481,BMG_DS006899,197927001;197924008;155901008,Recurrent urinary tract infection,,,,,,,C0262655,,,,,"Recurrent urinary tract infection | Recurrent UTI - urinary tract infection | Recurrent urinary tract infection (disorder) | Urinary tract infection, site not specified | Recurrent urinary tract infection | Urinary tract infection: [site not specified] or [recurrent] | Urinary tract infection: [site not specified] or [recurrent] (disorder) | Recurrent urinary tract infection | Recurrent urinary tract infection (disorder)"
+BMGC_DS04482,BMG_DS006903,,,,,,,DOID:4717,extragonadal germ cell cancer,C0262963,,,MONDO:0018201,extragonadal germ cell tumor,
+BMGC_DS04483,BMG_DS006915,23615008,Spongiotic dermatitis,,,,,DOID:4406,spongiotic dermatitis,C0262984,,MTHU057660,MONDO:0002987,spongiotic dermatitis,Spongiotic dermatitis | Spongiotic dermatitis (disorder)
+BMGC_DS04484,BMG_DS006916,238564003,Psoriasiform eczema,,,,,,,C0262985,,,,,Psoriasiform eczema | Psoriasiform eczema (disorder)
+BMGC_DS04485,BMG_DS006919,,Cutaneous Vasculitis,"Skin Diseases, Vascular",,,,,,C0262988,D017445,,MONDO:0020576,cutaneous vasculitis,
+BMGC_DS04486,BMG_DS007190,409784006,Contact dermatitis caused by urushiol from Pacific poison oak,,,,,,,C0263283,,,,,Contact dermatitis caused by urushiol from Toxicodendron diversilobum (disorder) | Contact dermatitis caused by Toxicodendron diversilobum | Contact dermatitis caused by urushiol from Toxicodendron diversilobum | Contact dermatitis caused by urushiol from Rhus diversiloba | Contact dermatitis caused by urushiol from Pacific poison oak
+BMGC_DS04487,BMG_DS007207,,Pemphigus Foliaceus,Pemphigus,,,,DOID:0080850,pemphigus foliaceus,C0263313,D010392,,MONDO:0019324,pemphigus foliaceus,
+BMGC_DS04488,BMG_DS007220,,"Urticaria, Aquagenic",Chronic Inducible Urticaria,,,,,,C0263334,D000094482,191850,MONDO:0008632,"urticaria, aquagenic",
+BMGC_DS04489,BMG_DS007224,,Chronic Urticaria,Chronic Urticaria,,,,DOID:0080747,chronic urticaria,C0263338,D000080223,,MONDO:0850230,chronic urticaria,
+BMGC_DS04490,BMG_DS007237,63501000,Prurigo nodularis,,EC91.0,Nodular prurigo,L28.1,,,C0263353,,,MONDO:0026045,prurigo nodularis,Prurigo nodularis | Hyde's disease | Prurigo nodularis (disorder) | Nodular prurigo | Picker's nodules
+BMGC_DS04491,BMG_DS007251,,Gianotti-Crosti Syndrome,Acrodermatitis,,,,,,C0263372,D000169,,,,
+BMGC_DS04492,BMG_DS007255,41580004,Distinctive exudative discoid AND lichenoid chronic dermatosis of Sulzberger and Garbe,,,,,,,C0263377,,,,,Distinctive exudative discoid AND lichenoid chronic dermatosis of Sulzberger and Garbe | Distinctive exudative discoid AND lichenoid chronic dermatosis of Sulzberger and Garbe (disorder) | Exudative discoid and lichenoid dermatosis | Sulzberger-Garbe syndrome
+BMGC_DS04493,BMG_DS007260,,Kyrle disease,,EE70.0,Acquired perforating dermatosis,L87.0,,,C0263382,C538130,149500,MONDO:0007869,Kyrle disease,
+BMGC_DS04494,BMG_DS007261,5132005;201062000,Keratosis pilaris,,,,,,,C0263383,C537412,MTHU005148,MONDO:0021036,keratosis pilaris,Keratosis pilaris | Keratosis pilaris (disorder) | KP - Keratosis pilaris | Keratosis pilaris | Keratosis pilaris (disorder)
+BMGC_DS04495,BMG_DS007262,,,,,,,,,C0263385,,167900,MONDO:0008188,"papillomatosis, confluent and reticulated",
+BMGC_DS04496,BMG_DS007272,58872001;201300002,Erythema elevatum diutinum,,EF40.2Y,Other specified localised cutaneous vasculitis,L95.1,DOID:0060567,erythema elevatum diutinum,C0263398,C535509,,MONDO:0019526,erythema elevatum diutinum,Erythema elevatum diutinum | Erythema elevatum diutinum (disorder) | EED - Erythema elevatum diutinum | Erythema elevatum diutinum | Erythema elevatum diutinum (disorder)
+BMGC_DS04497,BMG_DS007275,201304006;26825009,Cutis marmorata,,,,,,,C0263401,,MTHU005302,,,Cutis marmorata | Cutis marmorata (disorder) | Cutis marmorata | Cutis marmorata (finding)
+BMGC_DS04498,BMG_DS007276,8214000,Telangiectasia macularis eruptiva perstans,,,,D47.01,,,C0263402,C000715747,,MONDO:0019576,telangiectasia macularis eruptiva perstans,Telangiectasia macularis eruptiva perstans | Telangiectasia macularis eruptiva perstans (disorder) | TMEP - telangiectasia macularis eruptiva perstans | Paucicellular mastocytosis
+BMGC_DS04499,BMG_DS007279,,Linear Scleroderma,"Scleroderma, Localized",,,,,,C0263409,D012594,,MONDO:0043294,linear scleroderma,
+BMGC_DS04500,BMG_DS007285,28488007,Hyperkeratosis lenticularis perstans,,,,,,,C0263420,C538377,144150,MONDO:0007756,hyperkeratosis lenticularis perstans,Hyperkeratosis lenticularis perstans | Hyperkeratosis lenticularis perstans of Flegel | Hyperkeratosis lenticularis perstans (disorder) | Flegels disease
+BMGC_DS04501,BMG_DS007290,,Burnett Schwartz Berberian syndrome,,,,,,,C0263428,C537412,604093,MONDO:0018855,keratosis pilaris atrophicans,
+BMGC_DS04502,BMG_DS007291,2736005;201154005,Atrophoderma vermiculatum,,,,,,,C0263429,,209700,MONDO:0008849,atrophoderma vermiculata,Atrophoderma vermiculatum | Acne vermoulante | Honeycomb atrophy of face | Folliculitis ulerythematosa reticulata | Atrophoderma vermiculatum (disorder) | Atrophoderma vermiculatum | Atrophoderma vermiculatum (disorder)
+BMGC_DS04503,BMG_DS007311,83684005,Chloracne,Chloracne,,,,,,C0263454,D054506,,,,Chlorine acne | Chloracne | Chlorine acne (disorder)
+BMGC_DS04504,BMG_DS007323,201193001;47317002,Miliaria profunda,,EE02.Y,Other specified forms of miliaria,L74.2,DOID:0070320,miliaria profunda,C0263468,,,MONDO:0024228,miliaria profunda,Miliaria profunda | Miliaria profunda (disorder)
+BMGC_DS04505,BMG_DS007325,,Granulosis Rubra Nasi,,,,,,,C0263471,C562483,139000,MONDO:0007685,granulosis rubra nasi,
+BMGC_DS04506,BMG_DS007331,46586006,Diffuse alopecia areata,,,,,DOID:0060157,diffuse alopecia areata,C0263479,,,MONDO:0000687,diffuse alopecia areata,Diffuse alopecia areata | Diffuse alopecia areata (disorder)
+BMGC_DS04507,BMG_DS007338,247556005;21926007,Pili annulati,,EC21.0,Genetic defects of the hair shaft,Q84.1,,,C0263489,C537187,180600;MTHU010122,MONDO:0008388,ringed hair disease,Pili annulati | Pili annulati (disorder) | Pili annulati | Ringed hair | Pili annulati (disorder)
+BMGC_DS04508,BMG_DS007340,,,,,,,,,C0263491,,261900,MONDO:0009870,pili torti,
+BMGC_DS04509,BMG_DS007351,201145007;86166000,Alopecia universalis,,ED70.2Y,Other specified forms of alopecia areata,L63.1,DOID:0050634,alopecia universalis,C0263505,C537055,MTHU033161,MONDO:0800198,alopecia universalis,Alopecia universalis | Alopecia universalis (disorder) | Alopecia universalis | Alopecia universalis (disorder) | Universal alopecia areata
+BMGC_DS04510,BMG_DS007352,201182003,Perifolliculitis capitis abscedens,,ED70.51,Dissecting cellulitis,L66.3,,,C0263506,,260910,MONDO:0009848,dissecting cellulitis of the scalp,Perifolliculitis capitis abscedens | Perifolliculitis capitis abscedens (disorder)
+BMGC_DS04511,BMG_DS007362,201147004;39479004,Telogen effluvium,,ED70.3Z,Telogen effluvium unspecified,L65.0,DOID:1943,telogen effluvium,C0263518,,,MONDO:0002153,telogen effluvium,Telogen effluvium | Telogen effluvium (disorder)
+BMGC_DS04512,BMG_DS007406,80258006,Drug-induced lupus erythematosus,,,,,DOID:0040093,drug-induced lupus erythematosus,C0263591,,,MONDO:0016474,drug-induced lupus erythematosus,Drug-induced lupus erythematosus | Drug-induced lupus erythematosus (disorder) | Lupus-like syndrome
+BMGC_DS04513,BMG_DS007437,,,,,,,DOID:4028,angioma serpiginosum,C0263637,,,MONDO:0019803,angioma serpiginosum,
+BMGC_DS04514,BMG_DS007438,21848000,Angiokeratoma circumscriptum,,,,,DOID:5949,angiokeratoma circumscriptum,C0263638,,,MONDO:0003713,angiokeratoma circumscriptum,Angiokeratoma circumscriptum | Angiokeratoma circumscriptum (disorder)
+BMGC_DS04515,BMG_DS007439,,,,,,,DOID:664,angiokeratoma of Fordyce,C0263639,,,MONDO:0003954,angiokeratoma of Fordyce,
+BMGC_DS04516,BMG_DS007440,,,,,,,DOID:5948,angiokeratoma of mibelli,C0263640,,,MONDO:0003712,angiokeratoma of mibelli,
+BMGC_DS04517,BMG_DS007458,423486005;26328002,Disseminated eosinophilic collagen disease,,,,,DOID:9499,disseminated eosinophilic collagen disease,C0263662,,,MONDO:0004803,disseminated eosinophilic collagen disease,Disseminated eosinophilic collagen disease (disorder) | Disseminated eosinophilic collagen disease | Disseminated eosinophilic collagen disease | DECD | Hypereosinophilic syndrome | Disseminated eosinophilic collagen disease (disorder)
+BMGC_DS04518,BMG_DS007462,,"Dermatomyositis, Childhood Type",Dermatomyositis,,,,DOID:14203,childhood type dermatomyositis,C0263666,D003882,,MONDO:0008054,juvenile dermatomyositis,
+BMGC_DS04519,BMG_DS007583,,,,,,,DOID:13677,SAPHO syndrome,C0263859,,,MONDO:0019266,SAPHO syndrome,
+BMGC_DS04520,BMG_DS007611,268086004;6858004,Capsulitis,Bursitis,,,,,,C0263907,D002062,,,,(Peripheral enthesopathies) or (capsulitis) | Enthesopathies - peripheral | Capsulitis | Peripheral enthesopathies | (Peripheral enthesopathies) or (capsulitis) (disorder) | Capsulitis | Capsulitis (disorder)
+BMGC_DS04521,BMG_DS007635,156663001;11654001;268090002,Achilles tendinitis,,FB40.Y,Other specified tenosynovitis,M76.6,,,C0263933,,,,,Metatarsalgia | Calcaneal spur | Achilles tendinitis | Tendinitis of ankle/tarsus | Ankle tendonitis | Achilles tendiditis | Spur - calcaneal | (Tendinitis: [ankle/tarsus] or [achilles] or [ankle]) or (calcaneal spur) or (metatarsalgia) | (Tendinitis: [ankle/tarsus] or [achilles] or [ankle]) or (calcaneal spur) or (metatarsalgia) (disorder) | Achilles tendinitis | Achilles tendinitis (disorder) | Achilles tendonitis | (Tendinitis: [ankle/tarsus] or [achilles] or [ankle]) or (calcaneal spur) or (metatarsalgia) | Achilles tendiditis | Spur - calcaneal | Tendinitis of ankle/tarsus | Ankle tendonitis | Metatarsalgia | Calcaneal spur | Achilles tendinitis | (Tendinitis: [ankle/tarsus] or [achilles] or [ankle]) or (calcaneal spur) or (metatarsalgia) (disorder)
+BMGC_DS04522,BMG_DS007658,425940002;424548006;77299006;270542002;202930004,Olecranon bursitis,,FB50.Z,"Bursitis, unspecified",M70.2,DOID:12581,olecranon bursitis,C0263962,,,MONDO:0001557,olecranon bursitis,Inflammation of bursa of olecranon (disorder) | Capped elbow | Olecranon bursitis | Student's elbow | Inflammation of bursa of olecranon | Miner's elbow | Elbow hygroma (disorder) | Elbow hygroma | Olecranon bursitis | Bursitis of elbow | Miners' elbow | Bursitis of elbow region | Student's elbow | Olecranon bursitis (disorder) | Shoe boil | Capped elbow | Elbow bursitis (& olecranon) | Olecranon bursitis | Bursitis - elbow | Elbow bursitis (& olecranon) (disorder) | Olecranon bursitis | Olecranon bursitis (disorder)
+BMGC_DS04523,BMG_DS007668,,Polymyositis Ossificans,Polymyositis,,,,DOID:0080745,polymyositis,C0263984,D017285,,,,
+BMGC_DS04524,BMG_DS007680,16687001,Knuckle pads,,FB51.1,Knuckle pads,M72.1,,,C0264000,,149100;MTHU051342,MONDO:0007865,knuckle pads,Knuckle pads | Garrod's pads | Knuckle pads (disorder)
+BMGC_DS04525,BMG_DS007684,,Eosinophilic Fasciitis,,,,,,,C0264005,C562487,226350,MONDO:0009175,eosinophilic fasciitis,
+BMGC_DS04526,BMG_DS007687,28193003,Hepatic osteodystrophy,,,,,,,C0264010,,,,,Hepatic osteodystrophy | Hepatic osteodystrophy (disorder)
+BMGC_DS04527,BMG_DS007748,,Osteoarthropathy of fingers familial,,,,,,,C0264081,C537144,165700,MONDO:0008142,"Thiemann disease, familial form",
+BMGC_DS04528,BMG_DS007771,,,,,,,,,C0264115,,,MONDO:0024650,drug-induced osteoporosis,
+BMGC_DS04529,BMG_DS007775,,"Atrophy, Disuse","Muscular Disorders, Atrophic",,,,,,C0264122,D020966,,,,
+BMGC_DS04530,BMG_DS007782,,,,,,,,,C0264162,,,MONDO:0015271,idiopathic camptocormia,
+BMGC_DS04531,BMG_DS007815,17097001,Chronic disease of respiratory system,,,,,,,C0264220,,,,,Chronic respiratory disease | Chronic respiratory system disease | Chronic disease of respiratory system | Chronic disease of respiratory system (disorder)
+BMGC_DS04532,BMG_DS007878,,,,,,,,,C0264303,,150280,MONDO:0007878,congenital laryngomalacia,
+BMGC_DS04533,BMG_DS007892,81089005,Calcification of trachea,,,,,DOID:14224,tracheal calcification,C0264324,,,MONDO:0001911,tracheal calcification,Calcification of trachea | Calcification of trachea (disorder) | Tracheal calcification
+BMGC_DS04534,BMG_DS007909,54203008,Bronchomalacia,Bronchomalacia,,,,,,C0264353,D055091,MTHU014703,,,Bronchomalacia | Bronchomalacia (disorder)
+BMGC_DS04535,BMG_DS007912,,Cylindrical Bronchiectasis,Bronchiectasis,,,,,,C0264358,D001987,,,,
+BMGC_DS04536,BMG_DS007914,,Saccular Bronchiectasis,Bronchiectasis,,,,,,C0264360,D001987,,,,
+BMGC_DS04537,BMG_DS007944,,Panacinar Emphysema,Pulmonary Emphysema,,,,,,C0264393,D011656,,,,
+BMGC_DS04538,BMG_DS007964,,"Asthma, Occupational","Asthma, Occupational",,,,,,C0264423,D059366,,MONDO:0022742,occupational asthma,
+BMGC_DS04539,BMG_DS007973,36696005,Kaolinosis,,,,,DOID:10331,kaolin pneumoconiosis,C0264435,,,MONDO:0001005,kaolin pneumoconiosis,Kaolinosis | Kaolin pneumoconiosis | Kaolinosis (disorder) | Kaolin workers pneumoconiosis
+BMGC_DS04540,BMG_DS008010,65710008,Acute respiratory failure,,CB41.0Z,"Acute respiratory failure, unspecified",J96.0,DOID:11162,respiratory failure,C0264490,,,MONDO:0001208,acute respiratory failure,Acute respiratory failure | Acute respiratory failure (disorder) | ARF - Acute respiratory failure
+BMGC_DS04541,BMG_DS008019,,Compression Pulmonary Atelectasis,Pulmonary Atelectasis,,,,,,C0264499,D001261,,,,
+BMGC_DS04542,BMG_DS008027,,Endogenous Lipid Pneumonia,"Pneumonia, Lipid",,,,,,C0264510,D011017,,,,
+BMGC_DS04543,BMG_DS008028,44274007,Lymphoid interstitial pneumonia,,,,J84.2,,,C0264511,,247610;MTHU071516,MONDO:0009537,lymphoid interstitial pneumonia,Lymphoid interstitial pneumonia | Lymphocytic interstitial pneumonia | Lymphoid interstitial pneumonitis | Idiopathic lymphocytic interstitial pneumonia | Lymphoid interstitial pneumonitis (disorder)
+BMGC_DS04544,BMG_DS008031,,"Pneumonia, Necrotizing","Pneumonia, Necrotizing",,,,,,C0264515,D000071067,,,,
+BMGC_DS04545,BMG_DS008069,,Tension Pneumothorax,Pneumothorax,,,,,,C0264558,D011030,,,,
+BMGC_DS04546,BMG_DS008089,,Spastic Dysphonia,Dysphonia,,,,,,C0264588,D055154,,,,
+BMGC_DS04547,BMG_DS008099,,"Voice Disorder, Neurologic",Voice Disorders,,,,,,C0264600,D014832,,,,
+BMGC_DS04548,BMG_DS008106,,Apraxia of Phonation,Apraxias,,,,,,C0264611,D001072,,,,
+BMGC_DS04549,BMG_DS008167,413844008;84537008;194852007,Chronic myocardial ischemia,,,,,DOID:3393,coronary artery disease,C0264694,,,,,Chronic myocardial ischemia (disorder) | Chronic myocardial ischemia | Chronic myocardial ischaemia | Chronic coronary insufficiency | Chronic ischemic heart disease | Chronic myocardial ischemia | Chronic coronary insufficiency | Chronic ischaemic heart disease | Chronic myocardial ischaemia | Chronic ischemic heart disease (disorder) | Chronic myocardial ischaemia | Chronic myocardial ischemia | Chronic myocardial ischaemia (disorder)
+BMGC_DS04550,BMG_DS008181,195116000;56675007,Acute heart failure,,,,,,,C0264714,,,,,Acute heart failure | Acute heart failure (disorder)
+BMGC_DS04551,BMG_DS008183,48447003,Chronic heart failure,,,,,,,C0264716,,MTHU065635,,,Chronic heart failure | Chronic heart failure (disorder)
+BMGC_DS04552,BMG_DS008207,155265007;24363009,Rheumatic fever without heart involvement,,,,I00,DOID:1586,rheumatic fever,C0264743,,,,,Rheumatic fever without heart involvement | Rheumatic fever without heart involvement (disorder)
+BMGC_DS04553,BMG_DS008209,,Chorea Gravidarum,Chorea Gravidarum,,,,DOID:14483,chorea gravidarum,C0264746,D020150,,MONDO:0001976,chorea gravidarum,
+BMGC_DS04554,BMG_DS008226,83898004,Rheumatic disease of mitral valve,,,,,DOID:61,mitral valve disease,C0264765,,,MONDO:0042967,rheumatic disease of mitral valve,Rheumatic disease of mitral valve | Rheumatic mitral valve disease | Rheumatic mitral valve changes | Rheumatic disease of mitral valve (disorder)
+BMGC_DS04555,BMG_DS008234,194736003,Mitral and aortic incompetence,,,,,DOID:11502;DOID:57,mitral valve insufficiency | aortic valve insufficiency,C0264774,,,,,Mitral and aortic incompetence | Mitral and aortic insufficiency | Mitral and aortic regurgitation | Mitral and aortic incompetence (disorder)
+BMGC_DS04556,BMG_DS008236,49699002,Rheumatic tricuspid valve disease,,,,,DOID:0050826,tricuspid valve disease,C0264776,,,,,Rheumatic disease of tricuspid valve | Rheumatic tricuspid valve disease | Rheumatic disease of tricuspid valve (disorder)
+BMGC_DS04557,BMG_DS008247,389997000;195019009;35728003,Familial cardiomyopathy,,,,,,,C0264789,,,MONDO:0005217,familial cardiomyopathy,Familial cardiomyopathy | Familial cardiomyopathy (disorder) | Familial cardiomyopathy | Primary familial cardiomyopathy | Familial cardiomyopathy (disorder)
+BMGC_DS04558,BMG_DS008285,33258008,Primary eosinophilic endomyocardial restrictive cardiomyopathy,,,,,DOID:396,Loeffler endocarditis,C0264834,,,,,Primary eosinophilic endomyocardial restrictive cardiomyopathy | Eosinophilic endomyocardial disease | Löffler's endocarditis | Constrictive endocarditis | Löffler's parietal fibroplastic endocarditis | Primary eosinophilic endomyocardial restrictive cardiomyopathy (disorder)
+BMGC_DS04559,BMG_DS008330,42069006,Myxoid transformation of mitral valve,,,,,,,C0264885,,,,,Myxoid transformation of mitral valve | Myxomatous degeneration of mitral valve | Myxoid transformation of mitral valve (disorder)
+BMGC_DS04560,BMG_DS008331,44808001,Conduction disorder of the heart,,,,,,,C0264886,,115080,MONDO:0100042,cardiac conduction defect,Conduction disorder of the heart | Conduction disorder of the heart (disorder) | Disorder of heart conduction
+BMGC_DS04561,BMG_DS008336,195102005;71792006,Nodal rhythm disorder,,BE2Y,Other specified diseases of the circulatory system,I49.8,DOID:0110218;DOID:0110226,Brugada syndrome 1 | Brugada syndrome 9,C0264893,,,,,Nodal rhythm disorder | Nodal rhythm disorder (disorder) | Nodal rhythm disorder | Sinus arrhythmia | Nodal arrhythmia | Nodal rhythm disorder (disorder)
+BMGC_DS04562,BMG_DS008342,195042002,Second degree atrioventricular block,,,,,,,C0264906,,,MONDO:0000467,second-degree atrioventricular block,"Second degree atrioventricular block | Second degree atrioventricular block (disorder) | Incomplete atrioventricular block, second degree | Second degree heart block"
+BMGC_DS04563,BMG_DS008370,,Systemic Vasculitis,Systemic Vasculitis,,,,,,C0264939,D056647,,,,
+BMGC_DS04564,BMG_DS008409,34365005;195258006,Ruptured thoracic aortic aneurysm,,,,,DOID:3627,aortic aneurysm,C0265010,,,,,Ruptured thoracic aortic aneurysm | Ruptured thoracic aortic aneurysm (disorder) | Thoracic aortic aneurysm which has ruptured | Ruptured thoracic aortic aneurysm | Thoracic aortic aneurysm which has ruptured (disorder)
+BMGC_DS04565,BMG_DS008410,14336007,Ruptured abdominal aortic aneurysm,,,,,DOID:3627,aortic aneurysm,C0265012,,,,,Ruptured abdominal aortic aneurysm | Ruptured abdominal aortic aneurysm (disorder) | Abdominal aortic aneurysm which has ruptured | Ruptured aneurysm of abdominal aorta
+BMGC_DS04566,BMG_DS008419,57348003,Portal vein obstruction,,,,,,,C0265029,,,,,Portal vein obstruction | Portal vein obstruction (disorder) | Hepatic portal vein obstruction
+BMGC_DS04567,BMG_DS008437,40283005,Thrombophlebitis of superficial veins of lower extremity,,,,,DOID:3875,thrombophlebitis,C0265057,,,,,Thrombophlebitis of superficial veins of lower extremity | Thrombophlebitis of superficial veins of lower extremity (disorder)
+BMGC_DS04568,BMG_DS008445,195410000,Thrombophlebitis of the femoral vein,,,,,DOID:12282,femoral vein thrombophlebitis,C0265066,,,MONDO:0001481,femoral vein thrombophlebitis,Thrombophlebitis of the femoral vein | Thrombophlebitis of the femoral vein (disorder)
+BMGC_DS04569,BMG_DS008462,,Basilar Artery Stenosis,Vertebrobasilar Insufficiency,,,,,,C0265097,D014715,,,,
+BMGC_DS04570,BMG_DS008463,,,,,,,DOID:13446,basilar artery occlusion,C0265098,,,MONDO:0001715,basilar artery occlusion,
+BMGC_DS04571,BMG_DS008465,69798007;195181000;155397005;266254007,Carotid artery occlusion,,,,,,,C0265101,,,MONDO:0004450,carotid artery occlusion,"Carotid artery obstruction | Carotid artery obstruction (disorder) | Carotid artery occlusion (& [stenosis] or [thrombosis]) | Carotid artery thrombosis | Thrombosis, carotid artery | Stenosis, carotid artery | Carotid artery occlusion | Carotid artery occlusion (& [stenosis] or [thrombosis]) (disorder) | Carotid artery occlusion | Carotid artery occlusion (disorder) | Carotid artery occlusion | Occlusion of carotid artery (disorder) | Occlusion of carotid artery"
+BMGC_DS04572,BMG_DS008466,,Vertebral Artery Stenosis,Vertebrobasilar Insufficiency,,,,,,C0265103,D014715,,,,
+BMGC_DS04573,BMG_DS008470,,Cerebral Vasospasm,"Vasospasm, Intracranial",,,,,,C0265110,D020301,,,,
+BMGC_DS04574,BMG_DS008475,29322000,Acute cerebrovascular insufficiency,,,,I67.81,,,C0265115,,,,,Acute cerebrovascular insufficiency | Acute cerebrovascular insufficiency (disorder)
+BMGC_DS04575,BMG_DS008543,254201008;414673004,De Sanctis-Cacchione syndrome,,,,,DOID:0112158,De Sanctis-Cacchione syndrome,C0265201,C535992,278800,MONDO:0010217,de Sanctis-Cacchione syndrome,"De Sanctis-Cacchione syndrome | De Sanctis-Cacchione syndrome (disorder) | Mental retardation, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosa (disorder) | De Sanctis-Cacchione syndrome | Mental retardation, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosa | Xerodermic idiocy"
+BMGC_DS04576,BMG_DS008544,57917004,Seckel syndrome,,,,Q87.19,,,C0265202,,,MONDO:0019342,Seckel syndrome,Seckel syndrome | Bird-headed dwarf of Seckel | Nanocephalic dwarf | Bird-headed dwarf | Seckel syndrome (disorder)
+BMGC_DS04577,BMG_DS008546,,Robinow Syndrome,,,,,DOID:0060254,Robinow syndrome,C0265205,C562492,,MONDO:0019978,Robinow syndrome,
+BMGC_DS04578,BMG_DS008551,63119004,Weaver syndrome,,LD2C,Overgrowth syndromes,Q87.3,DOID:0080351,CLOVES syndrome,C0265210,C536687,277590,MONDO:0010193,Weaver syndrome,Weaver syndrome | Weaver syndrome (disorder)
+BMGC_DS04579,BMG_DS008552,73284007,Marshall-Smith syndrome,,,,,DOID:0050858,Marshall-Smith syndrome,C0265211,C536026,602535,MONDO:0011244,Marshall-Smith syndrome,"Marshall-Smith syndrome | Marshall-Smith syndrome (disorder) | Accelerated skeletal maturation, facial dysmorphism, failure to thrive syndrome"
+BMGC_DS04580,BMG_DS008554,24269006,Distal arthrogryposis syndrome,,,,,,,C0265213,,,MONDO:0019942,distal arthrogryposis,Distal arthrogryposis syndrome | Distal arthrogryposis syndrome (disorder) | Distal arthrogryposis
+BMGC_DS04581,BMG_DS008556,29076005,Meckel-Gruber syndrome,,GB8Z,"Cystic or dysplastic kidney disease, unspecified",Q61.9,DOID:0070119;DOID:0070118;DOID:0070115;DOID:0070120;DOID:0070117;DOID:0070116;DOID:0070122,Meckel syndrome 6 | Meckel syndrome 5 | Meckel syndrome 1 | Meckel syndrome 2 | Meckel syndrome 4 | Meckel syndrome 3 | Meckel syndrome 8,C0265215,,,MONDO:0018921,Meckel syndrome,Meckel-Gruber syndrome | Dysencephalia splanchnocystica | Meckel-Gruber syndrome (disorder)
+BMGC_DS04582,BMG_DS008557,71779008,X-linked hydrocephalus syndrome,,,,,,,C0265216,,307000,MONDO:0010611,X-linked hydrocephalus with stenosis of the aqueduct of Sylvius,X-linked hydrocephalus syndrome | Bickers-Adams syndrome | X-linked hydrocephalus | X-linked hydrocephalus syndrome (disorder)
+BMGC_DS04583,BMG_DS008559,253148005,Miller Dieker syndrome,,,,,DOID:0060469,Miller-Dieker lissencephaly syndrome,C0265219,,247200,MONDO:0009532,Miller-Dieker lissencephaly syndrome,Miller Dieker syndrome | Miller-Dieker syndrome | Miller-Dieker lissencephaly syndrome | Miller Dieker syndrome (disorder)
+BMGC_DS04584,BMG_DS008560,56677004,Pallister-Hall syndrome,,,,,DOID:9248,Pallister-Hall syndrome,C0265220,,146510,MONDO:0007804,Pallister-Hall syndrome,Pallister-Hall syndrome | Pallister-Hall syndrome (disorder)
+BMGC_DS04585,BMG_DS008561,111504002,Walker-Warburg congenital muscular dystrophy,,,,,,,C0265221,,,MONDO:0000171,"muscular dystrophy-dystroglycanopathy, type A","Walker-Warburg congenital muscular dystrophy | Walker-Warburg congenital muscular dystrophy (disorder) | Hydrocephalus, agyria and retinal dysplasia | Walker Warburg syndrome | HARD (hydrocephalus, agyria, retinal dysplasia) syndrome"
+BMGC_DS04586,BMG_DS008562,,Royer Syndrome,Prader-Willi Syndrome,,,,,,C0265222,D011218,,,,
+BMGC_DS04587,BMG_DS008563,,,,,,,DOID:0111590,Cohen syndrome,C0265223,,216550,MONDO:0008999,Cohen syndrome,
+BMGC_DS04588,BMG_DS008564,205799002;52616002,Freeman-Sheldon syndrome,,,,,DOID:0111604,Freeman-Sheldon syndrome,C0265224,C535483,193700,MONDO:0008675,Freeman-Sheldon syndrome,Whistling face syndrome | Freeman-Sheldon syndrome | Whistling face syndrome (disorder) | Freeman-Sheldon syndrome | Whistling face syndrome | Freeman-Sheldon syndrome (disorder) | Distal arthrogryposis type 2A
+BMGC_DS04589,BMG_DS008565,8757006,Hecht syndrome (disorder),,,,,,,C0265226,,158300,MONDO:0008016,trismus-pseudocamptodactyly syndrome,Hecht syndrome | Trismus pseudocamptodactyly syndrome | Hecht syndrome (disorder) | Distal arthrogryposis type 7 | Dutch Kentucky syndrome | Hecht Beals syndrome
+BMGC_DS04590,BMG_DS008566,18899000,Schinzel-Giedion syndrome,,,,,DOID:0070509,Schinzel Giedion syndrome,C0265227,C536632,269150,MONDO:0010010,Schinzel-Giedion syndrome,Schinzel-Giedion syndrome | Schinzel-Giedion syndrome (disorder)
+BMGC_DS04591,BMG_DS008570,34169006;204102004,Cryptophthalmos syndrome,,LD2Z,"Multiple developmental anomalies or syndromes, unspecified",Q87.0,DOID:0110716;DOID:0110719;DOID:0110718;DOID:0110717,Warburg micro syndrome 3 | Warburg micro syndrome 1 | Warburg micro syndrome 2 | Warburg micro syndrome 4,C0265233,,,MONDO:0009046,Fraser syndrome,"Fraser syndrome | Cryptophthalmos syndrome | Cryptophthalmos, defect of auricle AND genital anomaly | Fraser syndrome (disorder) | Cryptophthalmos syndrome | Cryptophthalmos syndrome (disorder) | Cryptophthalmos, defect of auricle AND genital anomaly | Fraser syndrome"
+BMGC_DS04592,BMG_DS008571,,Branchio-Oto-Renal Syndrome,Branchio-Oto-Renal Syndrome,,,,DOID:14702,branchiootorenal syndrome,C0265234,D019280,,MONDO:0007029,branchio-oto-renal syndrome,
+BMGC_DS04593,BMG_DS008572,33410002,Marshall syndrome,,,,,DOID:0111510,Marshall syndrome,C0265235,C536025,154780,MONDO:0007949,Marshall syndrome,Marshall syndrome | Marshall syndrome (disorder) | Marshall's syndrome
+BMGC_DS04594,BMG_DS008574,79665007,Wildervanck's syndrome,,,,,,,C0265239,,314600,MONDO:0010759,Wildervanck syndrome,Wildervanck's syndrome | Cervico-oculofacial syndrome | Wildervanck syndrome | Cervicooculoacoustic syndrome | Wildervanck syndrome (disorder)
+BMGC_DS04595,BMG_DS008575,,Goldenhar Syndrome,Goldenhar Syndrome,,,,DOID:2907,Goldenhar syndrome,C0265240,D006053,,MONDO:0015397,craniofacial microsomia,
+BMGC_DS04596,BMG_DS008577,,,,,,,,,C0265242,,202650,MONDO:0008740,agnathia-otocephaly complex,
+BMGC_DS04597,BMG_DS008579,35520007,Nager syndrome,,,,,,,C0265245,C538184,154400,MONDO:0007943,Nager acrofacial dysostosis,Nager syndrome | Nager acrofacial dysostosis syndrome | Preaxial acrofacial dysostosis | Nager syndrome (disorder)
+BMGC_DS04598,BMG_DS008580,24750000,Townes syndrome,,,,,,,C0265246,,,MONDO:0007142,Townes-Brocks syndrome,Townes syndrome | Townes syndrome (disorder) | Townes Brocks syndrome
+BMGC_DS04599,BMG_DS008581,,Ruvalcaba Syndrome,,,,,,,C0265248,C579395,180870,MONDO:0008395,Ruvalcaba syndrome,
+BMGC_DS04600,BMG_DS008582,,Mental retardation Mietens Weber type,,,,,,,C0265249,C537444,249600,MONDO:0009582,Mietens syndrome,
+BMGC_DS04601,BMG_DS008583,,Oto-Palato-digital syndrome type 1,,,,,DOID:0111783,otopalatodigital syndrome type 1,C0265251,C536065,311300,MONDO:0010704,otopalatodigital syndrome type 1,
+BMGC_DS04602,BMG_DS008584,15182000,Coffin-Lowry syndrome,,,,,DOID:3783,Coffin-Lowry syndrome,C0265252,,303600,MONDO:0010561,Coffin-Lowry syndrome,Coffin-Lowry syndrome | Coffin-Lowry syndrome (disorder) | CLS - Coffin-Lowry syndrome
+BMGC_DS04603,BMG_DS008585,78675000,Stickler syndrome (disorder),,,,,,,C0265253,,,MONDO:0019354,Stickler syndrome,Stickler syndrome | Hereditary arthro-ophthalmopathy | Wagner-Stickler syndrome | Stickler dysplasia | Hereditary progressive arthro-ophthalmopathy | Stickler syndrome (disorder)
+BMGC_DS04604,BMG_DS008586,18077009,Trichorhinophalangeal syndrome,,,,,,,C0265255,,,MONDO:0017951,trichorhinophalangeal syndrome,Trichorhinophalangeal syndrome | Trichorhinophalangeal syndrome (disorder)
+BMGC_DS04605,BMG_DS008587,,Genee-Wiedemann syndrome,,,,,DOID:0111259,postaxial acrofacial dysostosis,C0265257,C537680,263750,MONDO:0009903,postaxial acrofacial dysostosis,
+BMGC_DS04606,BMG_DS008589,66783006;205820002,Popliteal pterygium syndrome,,,,,DOID:0060055,popliteal pterygium syndrome,C0265259,,,MONDO:0017435,popliteal pterygium syndrome,Popliteal pterygium syndrome | Popliteal pterygium syndrome (disorder) | Popliteal pterygium syndrome | PPS - Popliteal pterygium syndrome | Popliteal pterygium syndrome (disorder)
+BMGC_DS04607,BMG_DS008590,,"Chondrodysplasia, Grebe type",,,,,,,C0265260,C537915,200700,MONDO:0008703,acromesomelic dysplasia 2A,
+BMGC_DS04608,BMG_DS008591,,,,,,,,,C0265261,,265000,MONDO:0009926,autosomal recessive multiple pterygium syndrome,
+BMGC_DS04609,BMG_DS008593,13280000,Femoral hypoplasia - unusual facies syndrome,,,,,,,C0265263,,134780,MONDO:0007604,femoral-facial syndrome,Femoral hypoplasia - unusual facies syndrome | Femoral hypoplasia - unusual facies syndrome (disorder) | Femoral facial syndrome
+BMGC_DS04610,BMG_DS008594,205814003;19092004,Holt-Oram syndrome,,LD2Z,"Multiple developmental anomalies or syndromes, unspecified",Q87.2,DOID:0060861;DOID:0060468;DOID:0090024,Holt-Oram syndrome | split hand-foot malformation 1 with sensorineural hearing loss | microphthalmia with limb anomalies,C0265264,C535326,142900,MONDO:0007732,Holt-Oram syndrome,Holt-Oram syndrome | Holt-Oram syndrome (disorder) | Holt-Oram syndrome | Holt-Oram syndrome (disorder) | Holt Oram syndrome | Heart-hand syndrome type 1 | Atriodigital dysplasia type 1
+BMGC_DS04611,BMG_DS008595,71988008,Aase syndrome,,,,,DOID:0111879,Diamond-Blackfan anemia 6,C0265265,C538442,,,,Aase syndrome | Aase syndrome (disorder) | Blackfan-Diamond anemia | Blackfan-Diamond anaemia | Aase Smith II syndrome | Congenital hypoplastic anaemia Blackfan-Diamond type | Congenital pure red cell aplasia | Congenital hypoplastic anemia Blackfan-Diamond type
+BMGC_DS04612,BMG_DS008596,,Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects,,,,,DOID:0111822,CHILD syndrome,C0265267,C562515,308050,MONDO:0010621,CHILD syndrome,
+BMGC_DS04613,BMG_DS008597,,,,,,,DOID:0060227,Adams-Oliver syndrome,C0265268,,,MONDO:0007034,Adams-Oliver syndrome,
+BMGC_DS04614,BMG_DS008598,,Lacrimoauriculodentodigital syndrome,,,,,,,C0265269,C538132,,MONDO:0007872,LADD syndrome,
+BMGC_DS04615,BMG_DS008599,,,,,,,,,C0265273,,200600,MONDO:0008701,achondrogenesis type IA,
+BMGC_DS04616,BMG_DS008600,,,,,,,,,C0265274,,600972,MONDO:0010966,achondrogenesis type IB,
+BMGC_DS04617,BMG_DS008601,75049004,Jeune thoracic dystrophy,,,,,,,C0265275,,,MONDO:0018770,Jeune syndrome,Jeune thoracic dystrophy | Asphyxiating thoracic dystrophy | Jeune thoracic dystrophy (disorder) | Jeune thoracic dysplasia | Jeune syndrome
+BMGC_DS04618,BMG_DS008602,240191008;53974002,Kniest dysplasia,,,,,DOID:0080045,Kniest dysplasia,C0265279,C537207,156550,MONDO:0007987,Kniest dysplasia,Kniest dysplasia | Kniest dysplasia (disorder) | Kniest dysplasia | Kniest syndrome | Kniest chondrodystrophy | Swiss cheese cartilage dysplasia | Kniest dysplasia (disorder)
+BMGC_DS04619,BMG_DS008603,,"Spondylometaphyseal dysplasia, Kozlowski type",,,,,DOID:0111554,spondylometaphyseal dysplasia Kozlowski type,C0265280,C535797,184252,MONDO:0008477,"spondylometaphyseal dysplasia, Kozlowski type",
+BMGC_DS04620,BMG_DS008604,,,,,,,DOID:0111514,metatropic dysplasia,C0265281,,156530,MONDO:0007986,metatropic dysplasia,
+BMGC_DS04621,BMG_DS008605,,,,,,,DOID:0060465,fibrochondrogenesis,C0265282,,,MONDO:0016068,fibrochondrogenesis,
+BMGC_DS04622,BMG_DS008606,,,,,,,,,C0265283,,108720,MONDO:0007167,atelosteogenesis type I,
+BMGC_DS04623,BMG_DS008607,82699004,Dyggve-Melchior-Clausen syndrome,,,,,,,C0265286,C535726,223800,MONDO:0009130,Dyggve-Melchior-Clausen disease,Dyggve-Melchior-Clausen syndrome | Dyggve-Melchior-Clausen syndrome (disorder) | Dyggve-Melchior-Clausen dysplasia
+BMGC_DS04624,BMG_DS008608,,,,,,,DOID:0111243,acromicric dysplasia,C0265287,,102370,MONDO:0007055,Acromicric dysplasia,
+BMGC_DS04625,BMG_DS008609,,Metaphyseal chondrodysplasia Schmid type,,,,,,,C0265289,C537352,156500,MONDO:0007983,Schmid metaphyseal chondrodysplasia,
+BMGC_DS04626,BMG_DS008610,,,,,,,,,C0265290,,,MONDO:0000138,metaphyseal chondrodysplasia,
+BMGC_DS04627,BMG_DS008612,,,,,,,,,C0265292,,,MONDO:0015465,craniometaphyseal dysplasia,
+BMGC_DS04628,BMG_DS008613,,,,,,,DOID:0111785,frontometaphyseal dysplasia,C0265293,,,MONDO:0015942,frontometaphyseal dysplasia,
+BMGC_DS04629,BMG_DS008614,27837003,Pyle metaphyseal dysplasia,,,,,,,C0265294,,265900,MONDO:0009943,Pyle disease,Pyle metaphyseal dysplasia | Pyle disease | Pyle's disease | Pyle metaphyseal dysplasia (disorder)
+BMGC_DS04630,BMG_DS008615,,Jansen type metaphyseal chondrodysplasia,,,,,,,C0265295,C537564,156400,MONDO:0007982,"metaphyseal chondrodysplasia, Jansen type",
+BMGC_DS04631,BMG_DS008619,17568006,Sclerosteosis,,,,,DOID:0060251,sclerosteosis,C0265301,C537525,,MONDO:0017838,sclerosteosis,Sclerosteosis | Sclerosteosis (disorder)
+BMGC_DS04632,BMG_DS008621,,,,,,,DOID:14761,Greig cephalopolysyndactyly syndrome,C0265306,,175700,MONDO:0008287,Greig cephalopolysyndactyly syndrome,
+BMGC_DS04633,BMG_DS008622,77608001,Baller-Gerold syndrome,,,,,DOID:0050654,Baller-Gerold syndrome,C0265308,C536788,218600,MONDO:0009039,Baller-Gerold syndrome,Baller-Gerold syndrome | Craniosynostosis-radial aplasia syndrome | Baller-Gerold syndrome (disorder)
+BMGC_DS04634,BMG_DS008623,17818006,Leri-Weill dyschondrosteosis,,,,,DOID:0060847,Leri-Weill dyschondrosteosis,C0265309,,127300,MONDO:0007481,Leri-Weill dyschondrosteosis,Leri-Weill dyschondrosteosis | Leri-Weill dyschondrosteosis (disorder) | Leri-Weill syndrome
+BMGC_DS04635,BMG_DS008626,2884008;205801004,Weill-Marchesani syndrome,,,,,DOID:0050475,Weill-Marchesani syndrome,C0265313,,,MONDO:0018096,Weill-Marchesani syndrome,Weill-Marchesani syndrome | Brachydactyly-spherophakia syndrome | Marchesani's syndrome | Brachymorphy with spherophakia syndrome | Weill-Marchesani syndrome (disorder) | Spherophakia-brachymorphia syndrome | Marchesani syndrome | WMS - Weill-Marchesani syndrome | Weill-Marchesani syndrome | Spherophakia-brachymorphia syndrome | Marchesani syndrome (disorder)
+BMGC_DS04636,BMG_DS008628,,Neurocutaneous Syndromes,Neurocutaneous Syndromes,,,,,,C0265316,D020752,,MONDO:0042983,neurocutaneous syndrome,
+BMGC_DS04637,BMG_DS008631,,,,,,,DOID:3852,Peutz-Jeghers syndrome,C0265323,,,,,
+BMGC_DS04638,BMG_DS008633,,Bannayan-Riley-Ruvalcaba Syndrome,"Hamartoma Syndrome, Multiple",,,,DOID:0050657,Bannayan-Riley-Ruvalcaba syndrome,C0265326,D006223,153480,MONDO:0007924,Bannayan-Riley-Ruvalcaba syndrome,
+BMGC_DS04639,BMG_DS008635,,Organoid Nevus Phakomatosis,"Nevus, Sebaceous of Jadassohn",,,,,,C0265329,D054000,,,,
+BMGC_DS04640,BMG_DS008636,7731005,Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder),,,,,,,C0265331,,,MONDO:0015884,autosomal dominant hypohidrotic ectodermal dysplasia,Autosomal dominant hypohidrotic ectodermal dysplasia syndrome | Rapp-Hodgkin ectodermal dysplasia syndrome | Anhidrotic ectodermal dysplasia | Rapp-Hodgkin type of ectodermal dysplasia | Anhidrotic ectodermal dysplasia syndrome | Hypohidrotic ectodermal dysplasia syndrome | Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)
+BMGC_DS04641,BMG_DS008637,38993008,Tricho-dento-osseous syndrome (disorder),,,,,DOID:0111565,trichodontoosseous syndrome,C0265333,,190320,MONDO:0008592,tricho-dento-osseous syndrome,Tricho-dento-osseous syndrome | TDO syndrome | Amelogenesis imperfecta - osteosclerosis syndrome | Taurodontism - curly hair - osteosclerosis syndrome | Tricho-dento-osseous syndrome (disorder) | TDO - Trichodento-osseous syndrome | Trichodento-osseous syndrome
+BMGC_DS04642,BMG_DS008638,,Pachyonychia Congenita,Pachyonychia Congenita,,,,DOID:0050449,pachyonychia congenita,C0265334,D053549,,MONDO:0016471,pachyonychia congenita,
+BMGC_DS04643,BMG_DS008640,2625009,Senter syndrome,,,,,,,C0265336,,148210,MONDO:0007850,autosomal dominant keratitis-ichthyosis-hearing loss syndrome,"Senter syndrome | Senter syndrome (disorder) | Autosomal dominant keratitis, ichthyosis, deafness syndrome | Autosomal dominant KID (keratitis, ichthyosis, deafness) syndrome"
+BMGC_DS04644,BMG_DS008641,10007009,Coffin-Siris syndrome,,,,,DOID:1925,Coffin-Siris syndrome,C0265338,C536436,,MONDO:0015452,Coffin-Siris syndrome,Coffin-Siris syndrome | Coffin-Siris syndrome (disorder)
+BMGC_DS04645,BMG_DS008642,21634003,Borjeson-Forssman-Lehmann syndrome,,,,,DOID:0050681,Borjeson-Forssman-Lehmann syndrome,C0265339,C536575,301900,MONDO:0010537,Borjeson-Forssman-Lehmann syndrome,Borjeson-Forssman-Lehmann syndrome | Borjeson-Forssman-Lehmann syndrome (disorder) | Borjeson syndrome
+BMGC_DS04646,BMG_DS008643,47507006,Rieger syndrome,,,,,DOID:14686,Axenfeld-Rieger syndrome,C0265341,,,MONDO:0019628,Rieger anomaly,Rieger syndrome | Rieger syndrome (disorder) | Rieger's syndrome | Rieger anomaly
+BMGC_DS04647,BMG_DS008644,,Cerebrocostomandibular Syndrome,,,,,DOID:0111248,cerebrocostomandibular syndrome,C0265342,C562538,117650,MONDO:0007301,cerebrocostomandibular syndrome,
+BMGC_DS04648,BMG_DS008645,61367005,Jarcho-Levin syndrome,,,,,,,C0265343,C537565,,MONDO:0000359,spondylocostal dysostosis,Jarcho-Levin syndrome | Spondylothoracic dysplasia | Jarcho-Levin syndrome (disorder) | Autosomal recessive spondylocostal dysostosis
+BMGC_DS04649,BMG_DS008646,,Donohue Syndrome,Donohue Syndrome,,,,DOID:0050470,Donohue syndrome,C0265344,D056731,246200,MONDO:0009517,Donohue syndrome,
+BMGC_DS04650,BMG_DS008647,,Lymphedema distichiasis syndrome,,,,,DOID:0111509,lymphedema-distichiasis syndrome,C0265345,C537710,153400,MONDO:0007922,lymphedema-distichiasis syndrome,
+BMGC_DS04651,BMG_DS008653,,CHARGE Syndrome,CHARGE Syndrome,,,,DOID:0050834,CHARGE syndrome,C0265354,D058747,214800,MONDO:0008965,CHARGE syndrome,
+BMGC_DS04652,BMG_DS008663,,Warfarin syndrome,,,,,,,C0265374,C536683,,MONDO:0016010,vitamin K-antagonist embryofetopathy,
+BMGC_DS04653,BMG_DS008724,9527009;395657006;395652000,Pallister-Killian syndrome,,,,,,,C0265449,,601803,MONDO:0011146,tetrasomy 12p,Killian-Teschler-Nicola syndrome | Pallister mosaic syndrome | Pallister-Killian syndrome | Isochromosome 12p syndrome | Tetrasomy 12p syndrome (disorder) | Tetrasomy 12p syndrome | Pallister-Killian syndrome (disorder) | Pallister-Killian syndrome | Tetrasomy 12p | Killian-Teschler-Nicola syndrome | Pallister mosaic syndrome | Pallister-Killian syndrome | Pallister-Killian syndrome (disorder)
+BMGC_DS04654,BMG_DS008757,,,,,,,DOID:0070622,ring chromosome 20 syndrome,C0265482,,,MONDO:0015436,ring chromosome 20,
+BMGC_DS04655,BMG_DS008768,26445008,Cat eye syndrome,,,,,,,C0265493,,115470,MONDO:0007276,cat-eye syndrome,Cat eye syndrome | Schachenmann's syndrome | Cat eye syndrome (disorder) | CES - Cat eye syndrome
+BMGC_DS04656,BMG_DS008774,,"49,XXXXY Syndrome",Klinefelter Syndrome,,,,,,C0265499,D007713,,MONDO:0019929,"49,XXXXY syndrome",
+BMGC_DS04657,BMG_DS008778,60399005,Dermatofibrosis lenticularis disseminata,,,,,DOID:0111536,Buschke-Ollendorff syndrome,C0265514,,166700,MONDO:0008157,Buschke-Ollendorff syndrome,Dermatofibrosis lenticularis disseminata | Buschke-Ollendorf syndrome | Dermato-osteopoikilosis | Dermatofibrosis lenticularis disseminata (disorder) | Disseminated dermatofibrosis
+BMGC_DS04658,BMG_DS008779,,,,,,,,,C0265535,,,MONDO:0000156,trigonocephaly,
+BMGC_DS04659,BMG_DS008780,,,,,,,,,C0265552,,155500,MONDO:0007962,megalodactyly,
+BMGC_DS04660,BMG_DS008781,,,,,,,DOID:0090020;DOID:0090023;DOID:0090027;DOID:0090026;DOID:0090025;DOID:0090022,split hand-foot malformation 4 | split hand-foot malformation 2 | split hand-foot malformation 3 | split hand-foot malformation 6 | split hand-foot malformation | split hand-foot malformation 5,C0265554,,,MONDO:0016576,split hand-foot malformation,
+BMGC_DS04661,BMG_DS008782,,,,,,,,,C0265559,,200500,MONDO:0008700,acheiropody,
+BMGC_DS04662,BMG_DS008783,,,,,,,,,C0265561,,,MONDO:0017469,congenital elbow dislocation,
+BMGC_DS04663,BMG_DS008784,,,,,,,,,C0265562,,,MONDO:0017468,congenital shoulder dislocation,
+BMGC_DS04664,BMG_DS008790,,,,,,,,,C0265581,,,MONDO:0019671,radial hemimelia,
+BMGC_DS04665,BMG_DS008798,,,,,,,,,C0265610,,,MONDO:0017461,familial isolated clinodactyly of fingers,
+BMGC_DS04666,BMG_DS008803,,,,,,,,,C0265633,,275220,MONDO:0010144,tibial hemimelia,
+BMGC_DS04667,BMG_DS008812,72951007,Gastroschisis,Gastroschisis,LB02,Gastroschisis,Q79.3,DOID:11044,gastroschisis,C0265706,D020139,MTHU009129;230750,MONDO:0009264,gastroschisis,Gastroschisis | Gastroschisis (disorder)
+BMGC_DS04668,BMG_DS008816,,,,,,,,,C0265756,,150300,MONDO:0007879,larynx atresia,
+BMGC_DS04669,BMG_DS008819,,,,,,,,,C0265780,,,MONDO:0020110,pulmonary agenesis,
+BMGC_DS04670,BMG_DS008820,,,,,,,,,C0265783,,,MONDO:0800133,pulmonary hypoplasia,
+BMGC_DS04671,BMG_DS008822,,,,,,,,,C0265797,,130710,MONDO:0007536,congenital lobar emphysema,
+BMGC_DS04672,BMG_DS008829,,,,,,,,,C0265843,,,MONDO:0019808,aortic valve atresia,
+BMGC_DS04673,BMG_DS008836,,,,,,,,,C0265857,,,MONDO:0018084,Uhl anomaly,
+BMGC_DS04674,BMG_DS008853,70041004,Erythrokeratodermia variabilis,,,,,DOID:0050467,erythrokeratodermia variabilis,C0265961,,,MONDO:0017851,erythrokeratodermia variabilis,Erythrokeratodermia variabilis | Erythrokeratodermia variabilis (disorder) | Congenital poikiloderma | Mendes da Costa syndrome
+BMGC_DS04675,BMG_DS008854,312514006;54336006,Ichthyosis linearis circumflexa,,,,,DOID:0050474,Netherton syndrome,C0265962,,MTHU010704,MONDO:0043106,ichthyosis linearis circumflexa,Netherton's syndrome | Comel-Netherton syndrome | Axial osteosclerosis with bamboo hair | Netherton syndrome | Netherton syndrome (disorder) | Ichthyosis linearis circumflexa | Ichthyosis linearis circumflexa (disorder)
+BMGC_DS04676,BMG_DS008855,,,,,,,DOID:0111339,Vohwinkel syndrome,C0265964,,124500,MONDO:0007422,keratoderma hereditarium mutilans,
+BMGC_DS04677,BMG_DS008856,,Dyskeratosis Congenita,Dyskeratosis Congenita,,,,DOID:2729,dyskeratosis congenita,C0265965,D019871,,MONDO:0015780,dyskeratosis congenita,
+BMGC_DS04678,BMG_DS008857,68897000;400014002,Hereditary benign intraepithelial dyskeratosis,,,,,,,C0265966,,127600,MONDO:0007486,hereditary benign intraepithelial dyskeratosis,Hereditary benign intraepithelial dyskeratosis | Witkop's disease | Witkop-Von Sallmann disease | Witkop's syndrome | Witkop-Brearley-Gentry syndrome | Witkop-von Sallman syndrome | Hereditary benign intraepithelial dyskeratosis (disorder) | Hereditary benign intraepithelial dyskeratosis (disorder) | Hereditary benign intraepithelial dyskeratosis | Witkop-von Sallman syndrome | Witkop-Von Sallmann disease
+BMGC_DS04679,BMG_DS008858,,"Porokeratosis, Disseminated Superficial Actinic",Porokeratosis,,,,DOID:3805,porokeratosis,C0265970,D017499,,MONDO:0019212,disseminated superficial actinic porokeratosis,
+BMGC_DS04680,BMG_DS008859,,Acrokeratosis Verruciformis of Hopf,Darier Disease,,,,,,C0265971,D007644,101900,MONDO:0007048,acrokeratosis verruciformis,
+BMGC_DS04681,BMG_DS008862,,,,,,,DOID:4702,mongolian spot,C0265985,,,MONDO:0006582,mongolian spot,
+BMGC_DS04682,BMG_DS008863,,,,,,,,,C0265987,,617025,MONDO:0014873,nevus comedonicus syndrome,
+BMGC_DS04683,BMG_DS008867,,,,,,,,,C0265998,,206800,MONDO:0008798,nonsyndromic congenital nail disorder 4,
+BMGC_DS04684,BMG_DS008868,,,,,,,,,C0266000,,149300,MONDO:0007867,nonsyndromic congenital nail disorder 2,
+BMGC_DS04685,BMG_DS008869,,"Knuckle pads, leuconychia and sensorineural deafness",,,,,,,C0266004,C537210,149200,MONDO:0007866,Bart-Pumphrey syndrome,
+BMGC_DS04686,BMG_DS008870,67817003,Pili torti-deafness syndrome,,,,,DOID:0050677,Bjornstad syndrome,C0266006,,262000,MONDO:0009872,Bjornstad syndrome,Pili torti-deafness syndrome | Bjornstad's syndrome | Pili torti-deafness syndrome (disorder)
+BMGC_DS04687,BMG_DS008872,,,,,,,,,C0266011,,163700,MONDO:0008101,familial supernumerary nipples,
+BMGC_DS04688,BMG_DS008875,,,,,,,,,C0266029,,168200,MONDO:0008194,Paramolar tubercle of bolk,
+BMGC_DS04689,BMG_DS008877,51744007,Taurodontism,,LA30.4,Abnormalities of size or form of teeth,K00.2,,,C0266039,C536946,272700;MTHU007744,MONDO:0010098,taurodontism,Taurodontism | Taurodontism (disorder)
+BMGC_DS04690,BMG_DS008889,,,,,,,,,C0266159,,265950,MONDO:0009944,pyloric atresia,
+BMGC_DS04691,BMG_DS008890,,,,,,,,,C0266172,,243600,MONDO:0009476,atresia of small intestine,
+BMGC_DS04692,BMG_DS008891,,,,,,,,,C0266174,,223400,MONDO:0009126,duodenal atresia,
+BMGC_DS04693,BMG_DS008897,,,,,,,,,C0266251,,137040,MONDO:0007642,isolated agenesis of gallbladder,
+BMGC_DS04694,BMG_DS008900,,,,,,,,,C0266283,,,MONDO:0019854,thyroid ectopia,
+BMGC_DS04695,BMG_DS008901,,,,,,,,,C0266294,,,MONDO:0019636,"renal agenesis, unilateral",
+BMGC_DS04696,BMG_DS008902,,,,,,,,,C0266295,,,MONDO:0019637,renal hypoplasia,
+BMGC_DS04697,BMG_DS008903,702397002,Allanson Pantzar McLeod syndrome,,,,,,,C0266313,C537048,,MONDO:0017609,renal tubular dysgenesis,Renal tubular dysgenesis (disorder) | Primitive renal tubule syndrome | Allanson Pantzar McLeod syndrome | Renal tubular dysgenesis
+BMGC_DS04698,BMG_DS008909,,"Hermaphroditism, True",Ovotesticular Disorders of Sex Development,,,,,,C0266361,D050090,,MONDO:0002768,true hermaphroditism,
+BMGC_DS04699,BMG_DS008910,,,,,,,,,C0266383,,192000,MONDO:0008635,uterine anomalies,
+BMGC_DS04700,BMG_DS008917,53599007;236797008,Testicular regression syndrome,,,,,,,C0266427,C537770,273250,MONDO:8000015,"46,XY sex reversal 11",Testicular regression syndrome | Vanishing testes syndrome | Testicular regression - embryonic | XY Gonadal agenesis syndrome | Testicular regression syndrome (disorder) | Testicular regression syndrome | XY Gonadal agenesis syndrome | Testicular regression - embryonic | Testicular regression syndrome (disorder)
+BMGC_DS04701,BMG_DS008918,,,,,,,,,C0266432,,238320,MONDO:0009384,"Leydig cell hypoplasia, type 1",
+BMGC_DS04702,BMG_DS008920,,,,,,,DOID:0050453,lissencephaly,C0266463,,,MONDO:0018838,lissencephaly spectrum disorders,
+BMGC_DS04703,BMG_DS008921,,,,,,,,,C0266464,,,MONDO:0000087,polymicrogyria,
+BMGC_DS04704,BMG_DS008922,,,,,,,DOID:0060264,pontocerebellar hypoplasia,C0266468,,,,,
+BMGC_DS04705,BMG_DS008924,,,,,,,DOID:0050453,lissencephaly,C0266483,,,,,
+BMGC_DS04706,BMG_DS008925,,,,,,,,,C0266484,,269160,MONDO:0010011,schizencephaly,
+BMGC_DS04707,BMG_DS008926,,Etat Marbre,Movement Disorders,,,,,,C0266487,D009069,,,,
+BMGC_DS04708,BMG_DS008928,253150002;448041008,Neuronal heterotopia,,,,,,,C0266491,,MTHU060692,,,Neuronal heterotopia | Neuronal heterotopia (disorder) | Neuronal heterotopia (morphologic abnormality) | Cortical heterotopia | Grey matter heterotopia | Neuronal heterotopia | Gray matter heterotopia
+BMGC_DS04709,BMG_DS008932,,Marcus Gunn phenomenon,,,,,DOID:560,jaw-winking syndrome,C0266521,C535908,154600,MONDO:0007946,jaw-winking syndrome,
+BMGC_DS04710,BMG_DS008933,,,,,,,DOID:0060844,Norrie disease,C0266526,,310600,MONDO:0010691,Norrie disease,
+BMGC_DS04711,BMG_DS008936,,,,,,,,,C0266537,,116800,MONDO:0007290,cataract 5 multiple types,
+BMGC_DS04712,BMG_DS008937,,,,,,,,,C0266539,,,MONDO:0021548,total early-onset cataract,
+BMGC_DS04713,BMG_DS008938,,,,,,,,,C0266548,,,MONDO:0020368,Axenfeld anomaly,
+BMGC_DS04714,BMG_DS008939,,,,,,,DOID:0060282,persistent hyperplastic primary vitreous,C0266568,,,MONDO:0019631,persistent hyperplastic primary vitreous,
+BMGC_DS04715,BMG_DS008940,,,,,,,DOID:0060261,congenital ptosis,C0266573,,,,,
+BMGC_DS04716,BMG_DS008944,,,,,,,,,C0266589,,128600,MONDO:0007500,ear malformation,
+BMGC_DS04717,BMG_DS008947,,,,,,,,,C0266667,,236100,MONDO:0009349,holoprosencephaly 1,
+BMGC_DS04718,BMG_DS008957,79222000,Compression of umbilical cord,,,,,,,C0266798,,,,,Compression of umbilical cord | Compression of umbilical cord (disorder)
+BMGC_DS04719,BMG_DS008976,,"Visceral Myopathy, Familial",,,,,,,C0266833,C562574,,MONDO:0016829,familial visceral myopathy,
+BMGC_DS04720,BMG_DS008981,442551007,Dental caries extending into dentin,,,,,DOID:10461,dentin caries,C0266846,,,MONDO:0001041,dentin caries,Dental caries extending into dentine | Dentine caries | Dentin caries | Dental caries extending into dentin | Dental caries extending into dentin (disorder)
+BMGC_DS04721,BMG_DS008985,80353004,Enamel caries,,,,,DOID:217,enamel caries,C0266853,,,MONDO:0002233,enamel caries,Enamel caries | Simple dental caries | Dental caries confined to enamel | Simple dental cavity | Enamel caries (disorder) | Cavitated lesion limited to enamel
+BMGC_DS04722,BMG_DS009004,41918006,External resorption of tooth,,,,,DOID:14529,external pathological resorption,C0266878,,,MONDO:0001988,external pathological resorption,External resorption of tooth | Pathological tooth resorption - external | External resorption of root of tooth | External resorption of tooth (disorder)
+BMGC_DS04723,BMG_DS009018,,Periapical abscess with sinus,,DA09.61,Periapical abscess with sinus,K04.6,DOID:0060324,dental abscess,C0266909,,,,,
+BMGC_DS04724,BMG_DS009022,59898000,Localized gingival recession,,,,,DOID:1134,gingival recession,C0266916,,,,,Localized gingival recession | Localised gingival recession | Localized gingival recession (disorder)
+BMGC_DS04725,BMG_DS009025,,Epulides,Gingival Diseases,,,,DOID:5337,epulis,C0266919,D005882,,MONDO:0003396,epulis,
+BMGC_DS04726,BMG_DS009033,,Chronic Periodontitis,Chronic Periodontitis,,,,,,C0266929,D055113,260950,MONDO:0009850;MONDO:0005593,"periodontitis, chronic, adult | chronic periodontitis",
+BMGC_DS04727,BMG_DS009077,45517002,Benign lymphoepithelial lesion of salivary gland,,DA04.Z,"Diseases of salivary glands, unspecified",K11.8,DOID:12899,benign lymphoepithelial lesion of salivary gland,C0266995,,,MONDO:0001598,benign lymphoepithelial lesion of salivary gland,Benign lymphoepithelial lesion of salivary gland | Benign lymphoepithelial salivary gland lesion | Benign lymphoepithelial lesion of salivary gland (disorder)
+BMGC_DS04728,BMG_DS009080,,Vesicular Stomatitis,Vesicular Stomatitis,,,,,,C0266999,D054243,,MONDO:0025028,vesicular stomatitis,
+BMGC_DS04729,BMG_DS009095,200839009;46795000,Actinic cheilitis,,,,,,,C0267026,C535669,,MONDO:0043300,actinic cheilitis,Actinic cheilitis | Actinic cheilitis (disorder) | Actinic cheilitis | Solar keratosis of lip | Actinic cheilitis (disorder)
+BMGC_DS04730,BMG_DS009114,40719004,Erosive esophagitis,,,,,,,C0267055,,,,,Erosive esophagitis | Erosive oesophagitis | Erosive esophagitis (disorder)
+BMGC_DS04731,BMG_DS009126,,Oropharyngeal Dysphagia,Deglutition Disorders,,,,,,C0267071,D003680,,,,
+BMGC_DS04732,BMG_DS009127,,Esophageal Dysphagia,Deglutition Disorders,,,,,,C0267072,D003680,,,,
+BMGC_DS04733,BMG_DS009136,,,,,,,DOID:9021,esophageal leukoplakia,C0267095,,,MONDO:0004697,esophageal leukoplakia,
+BMGC_DS04734,BMG_DS009146,18665000,Acute gastric mucosal erosion,,,,,,,C0267112,,,,,Acute gastric mucosal erosion | Acute erosion of stomach | Acute gastric mucosal erosion (disorder)
+BMGC_DS04735,BMG_DS009184,66329006;196738004,Eosinophilic gastritis,,,,,DOID:4030,eosinophilic gastritis,C0267154,C535952,,MONDO:0002840,eosinophilic gastritis,Eosinophilic gastritis | Eosinophilic gastritis (disorder)
+BMGC_DS04736,BMG_DS009203,713704004,Gastroparesis due to diabetes mellitus,,,,,,,C0267176,,,,,Gastroparesis due to diabetes mellitus (disorder) | Gastroparesis due to diabetes mellitus | Gastroparesis with diabetes mellitus
+BMGC_DS04737,BMG_DS009207,54051005,Cascade stomach,,,,,DOID:12234,cascade stomach,C0267183,,,MONDO:0001469,cascade stomach,Cascade stomach | Cascade stomach (disorder)
+BMGC_DS04738,BMG_DS009227,,Gastric Antral Vascular Ectasia,Gastric Antral Vascular Ectasia,,,,DOID:2493,gastric antral vascular ectasia,C0267211,D020252,,MONDO:0006767,gastric antral vascular ectasia,
+BMGC_DS04739,BMG_DS009295,196684004;12274003;155702008,Acute peptic ulcer with hemorrhage,,,,,,,C0267288,,,,,Acute peptic ulcer with haemorrhage | Acute peptic ulcer with hemorrhage | Acute peptic ulcer with hemorrhage (disorder) | Acute peptic ulcer with hemorrhage | Acute peptic ulcer with haemorrhage | Acute peptic ulcer with hemorrhage (disorder) | Acute peptic ulcer with haemorrhage | Acute peptic ulcer with hemorrhage | Acute peptic ulcer with haemorrhage (disorder)
+BMGC_DS04740,BMG_DS009344,235853006,Angiodysplasia of intestine,,,,,DOID:10846,angiodysplasia of intestine,C0267367,,,MONDO:0001138,angiodysplasia of intestine,Angiodysplasia of intestine | Intestinal vascular dysplasia | Angiodysplasia of intestine (disorder) | Angiectasia of intestine | Vascular ectasia of intestine
+BMGC_DS04741,BMG_DS009350,54597004,Chronic colitis,,,,,,,C0267375,,,,,Chronic colitis | Chronic colitis (disorder)
+BMGC_DS04742,BMG_DS009360,14311001,Severe chronic ulcerative colitis,,,,,,,C0267387,,,,,Severe chronic ulcerative colitis | Fulminant ulcerative colitis | Severe chronic ulcerative colitis (disorder)
+BMGC_DS04743,BMG_DS009363,52506002,Chronic ulcerative rectosigmoiditis,,,,,,,C0267390,,,MONDO:0007005,ulcerative proctosigmoiditis,Chronic ulcerative rectosigmoiditis | Chronic ulcerative proctosigmoiditis | Ulcerative rectosigmoiditis | Ulcerative colitis confined to rectum and sigmoid colon | Ulcerative proctosigmoiditis | Chronic ulcerative rectosigmoiditis (disorder)
+BMGC_DS04744,BMG_DS009405,69980003,Non-infective diarrhea,,,,,,,C0267436,,,MONDO:0045030,non-infectious diarrheal disease,Non-infective diarrhea | Non-infective diarrhoea | Non-infective diarrhea (disorder) | Presumed non-infectious diarrhoea | Presumed non-infectious diarrhea
+BMGC_DS04745,BMG_DS009427,23065003,Stenosis of intestine,,,,,,,C0267465,,,,,Stenosis of intestine | Enterostenosis | Stenosis of intestine (disorder)
+BMGC_DS04746,BMG_DS009444,197253001;46040000,Ulceration of colon,,,,,,,C0267491,,,,,Ulceration of colon | Ulceration of colon (disorder) | Ulceration of colon | Colonic ulcer | Ulceration of colon (disorder)
+BMGC_DS04747,BMG_DS009450,48241004,Meckel's diverticulitis,,,,,DOID:8408,Meckel's diverticulitis,C0267497,,,MONDO:0004551,Meckel diverticulitis,Meckel's diverticulitis | Meckel's diverticulitis (disorder) | Meckel diverticulitis
+BMGC_DS04748,BMG_DS009455,56165008;280991008,Diverticulitis of small intestine,,,,,DOID:11223,small intestine diverticulitis,C0267502,,,MONDO:0001229,small intestine diverticulitis,Diverticulitis of small intestine | Diverticulitis of small intestine (disorder)
+BMGC_DS04749,BMG_DS009461,82934008,Chronic idiopathic constipation,,,,K59.04,,,C0267509,,,,,Chronic idiopathic constipation | Chronic idiopathic constipation (disorder)
+BMGC_DS04750,BMG_DS009504,65979008,Drug and toxin-induced diarrhea,,,,,,,C0267558,,,,,Drug AND/OR toxin-induced diarrhea | Drug AND/OR toxin-induced diarrhoea | Drug AND/OR toxin-induced diarrhea (disorder)
+BMGC_DS04751,BMG_DS009580,24412005,Congenital chloride diarrhea,,,,,DOID:0060296,congenital secretory chloride diarrhea 1,C0267662,C536210,214700,MONDO:0008964,congenital secretory chloride diarrhea 1,"Congenital secretory diarrhea, chloride type | Congenital chloridorrhea | Defective Cl^-^/HCO^-^>3< exchange in ileum AND/OR colon | Congenital chloridorrhoea | Congenital secretory diarrhoea, chloride type | Congenital secretory diarrhea, chloride type (disorder) | Congenital chloride diarrhoea | Congenital chloride diarrhea"
+BMGC_DS04752,BMG_DS009581,18805001,"Congenital secretory diarrhea, sodium type (disorder)",,,,,,,C0267663,,,MONDO:0015170,congenital sodium diarrhea,"Congenital secretory diarrhea, sodium type | Congenital sodium diarrhea | Defective Na^+^/H^+^ exchange in jejunum AND/OR ileum | Congenital secretory diarrhoea, sodium type | Congenital sodium diarrhoea | Congenital secretory diarrhea, sodium type (disorder) | Non-syndromic congenital sodium diarrhoea | Non-syndromic congenital sodium diarrhea"
+BMGC_DS04753,BMG_DS009603,3662000,Paraesophageal hernia,,,,,DOID:12642,hiatus hernia,C0267725,,MTHU038976,,,Paraesophageal hernia | Thoracic stomach | Gastroesophageal hernia | Rolling hiatus hernia | Paraoesophageal hiatus hernia | Paraoesophageal hernia | Paraesophageal hiatus hernia | Paraesophageal hernia (disorder) | Gastrooesophageal hernia
+BMGC_DS04754,BMG_DS009647,,Hepatobiliary Disorder,Digestive System Diseases,,,,DOID:3118,hepatobiliary disease,C0267792,D004066,,MONDO:0002515,hepatobiliary disorder,
+BMGC_DS04755,BMG_DS009652,37871000,Acute hepatitis,,,,,,,C0267797,,MTHU023293,,,Acute hepatitis | Acute hepatitis (disorder)
+BMGC_DS04756,BMG_DS009664,,"Cirrhosis, Cryptogenic",,,,,,,C0267809,C562577,,,,
+BMGC_DS04757,BMG_DS009682,197373008;301031003;85057007,Liver cyst,,,,,,,C0267834,,,,,Liver cyst | Liver cyst (disorder) | Hepatic cyst | Cyst of liver | Liver cyst | Cyst of liver (disorder)
+BMGC_DS04758,BMG_DS009687,,Acalculous Cholecystitis,Acalculous Cholecystitis,,,,DOID:2828,acalculous cholecystitis,C0267841,D042101,,MONDO:0006633,acalculous cholecystitis,
+BMGC_DS04759,BMG_DS009748,6215006,Acute cholangitis,,,,,DOID:14271,acute cholangitis,C0267917,,MTHU060449,MONDO:0001930,acute cholangitis,Acute cholangitis | Acute cholangitis (disorder)
+BMGC_DS04760,BMG_DS009749,71912000,Chronic cholangitis,,,,,DOID:9439,chronic cholangitis,C0267918,,,MONDO:0004786,chronic cholangitis,Chronic cholangitis | Chronic cholangitis (disorder)
+BMGC_DS04761,BMG_DS009750,17266006,Primary cholangitis,,,,K83.09,,,C0267919,,,,,Primary cholangitis | Primary cholangitis (disorder)
+BMGC_DS04762,BMG_DS009754,69850007;197437002,Suppurative cholangitis,,,,K83.09,DOID:14269,suppurative cholangitis,C0267924,,,MONDO:0001928,suppurative cholangitis,Suppurative cholangitis | Suppurative cholangitis (disorder)
+BMGC_DS04763,BMG_DS009765,,"Pancreatitis, Acute Hemorrhagic","Pancreatitis, Acute Hemorrhagic",,,,DOID:0080999,acute hemorrhagic pancreatitis,C0267940,D000081032,,MONDO:0850421,acute hemorrhagic pancreatitis,
+BMGC_DS04764,BMG_DS009766,,Pancreatitis Necrotizing,"Pancreatitis, Acute Necrotizing",,,,DOID:0080998,acute necrotizing pancreatitis,C0267941,D019283,,MONDO:0850420,acute necrotizing pancreatitis,
+BMGC_DS04765,BMG_DS009777,,Peripancreatic Fat Necrosis,Pancreatitis,,,,,,C0267954,D010195,,,,
+BMGC_DS04766,BMG_DS009784,47367009,Exocrine pancreatic insufficiency,,,,K86.81,DOID:13316,exocrine pancreatic insufficiency,C0267963,,MTHU010290,MONDO:0001684,exocrine pancreatic insufficiency,Exocrine pancreatic insufficiency | Exocrine pancreatic insufficiency (disorder) | Pancreatic exocrine insufficiency | EPI - exocrine pancreatic insufficiency
+BMGC_DS04767,BMG_DS009823,26436007,Disorder of acid-base balance,,,,,,,C0268029,,,MONDO:0041261,disorder of acid-base balance,Disorder of acid-base balance | Disturbance of acid-base balance | Disorder of acid-base balance (disorder)
+BMGC_DS04768,BMG_DS009850,6160004,Neonatal hemochromatosis,,,,P78.84,,,C0268059,C536394,MTHU023490;231100,MONDO:0009275,neonatal hemochromatosis,Neonatal hemochromatosis | Idiopathic neonatal hemochromatosis | Idiopathic neonatal haemochromatosis | Neonatal haemochromatosis | Neonatal hemochromatosis (disorder)
+BMGC_DS04769,BMG_DS009851,50855007,Juvenile hemochromatosis,,,,,DOID:0111034,hemochromatosis type 2,C0268060,C537247,,MONDO:0019257,hemochromatosis type 2,Juvenile hemochromatosis | Juvenile haemochromatosis | Juvenile hemochromatosis (disorder) | Haemochromatosis type 2 | Hemochromatosis type 2
+BMGC_DS04770,BMG_DS009861,19577007,Hypocupremia,,,,,,,C0268070,,,,,Hypocupremia | Chronic copper deficiency | Copper deficiency | Hypocupraemia | Hypocupremia (disorder)
+BMGC_DS04771,BMG_DS009869,,"Hypercalcemia, Idiopathic, of Infancy",,,,,,,C0268080,C562581,,,,
+BMGC_DS04772,BMG_DS009878,46939000,Keshan disease,,,,E59,DOID:0050083,Keshan disease,C0268095,C536166,,MONDO:0000241,Keshan disease,Keshan disease | Congestive cardiomyopathy due to selenium deficiency | Keshan disease (disorder)
+BMGC_DS04773,BMG_DS009887,68451005,Chronic gouty arthritis,,,,,,,C0268108,,,,,Chronic gouty arthritis | Chronic gouty arthritis (disorder) | Chronic arthritis due to gout | Chronic articular gout
+BMGC_DS04774,BMG_DS009895,,"Gout, HPRT-Related",,,,,,,C0268117,C562583,300323,MONDO:0010299,hypoxanthine guanine phosphoribosyltransferase partial deficiency,
+BMGC_DS04775,BMG_DS009896,,"Xanthinuria, Type I",,,,,DOID:0070452,xanthinuria type I,C0268118,C562584,278300,MONDO:0010209,xanthinuria type I,
+BMGC_DS04776,BMG_DS009897,29692004,Combined molybdoflavoprotein enzyme deficiency,,,,,,,C0268119,,,MONDO:0020480,sulfite oxidase deficiency due to molybdenum cofactor deficiency,"Combined molybdoflavoprotein enzyme deficiency | Hereditary xanthinuria, type 2 | Deficiency of molybdenum cofactor | Xanthine oxidase-sulfite oxidase deficiency | Hereditary xanthinuria type 2 | Molybdenum cofactor deficiency | Combined xanthine oxidase and aldehyde oxidase deficiency | Xanthine oxidase-sulphite oxidase deficiency | Combined xanthine oxidase and sulfite oxidase and aldehyde oxidase deficiency | Combined xanthine oxidase and sulphite oxidase and aldehyde oxidase deficiency | Combined molybdoflavoprotein enzyme deficiency (disorder)"
+BMGC_DS04777,BMG_DS009898,11852004,Adenine phosphoribosyltransferase deficiency,,,,,DOID:0060350,adenine phosphoribosyltransferase deficiency,C0268120,C538228,614723,MONDO:0013869,adenine phosphoribosyltransferase deficiency,Adenine phosphoribosyltransferase deficiency | Adenine phosphoribosyltransferase deficiency (disorder)
+BMGC_DS04778,BMG_DS009899,65791008,"APRT deficiency, Japanese type",,,,,,,C0268121,,,,,"APRT deficiency, Japanese type | Adenine phosphoribosyltransferase (APRT) deficiency, Japanese type | Adenine phosphoribosyltransferase deficiency, Japanese type (disorder) | Adenine phosphoribosyltransferase deficiency, Japanese type"
+BMGC_DS04779,BMG_DS009902,44940001;190999009;190738006,Adenosine deaminase deficiency,,,,,DOID:5810,adenosine deaminase deficiency,C0268124,C531816,,,,Adenosine deaminase deficiency | ADA deficiency | Adenosine aminohydrolase deficiency | Adenosine deaminase deficiency (disorder) | ADA - Adenosine aminohydrolase deficiency | Deficiency of adenosine deaminase | Adenosine deaminase deficiency | Adenosine deaminase deficiency (disorder) | (Adenosine deaminase deficiency) or (other specified disturbance of amino acid metabolism) | Adenosine-deaminase deficiency | Adenosine deaminase deficiency | Other specified disturbance of amino-acid metabolism | (Adenosine deaminase deficiency) or (other specified disturbance of amino acid metabolism) (disorder)
+BMGC_DS04780,BMG_DS009903,60743005,Purine-nucleoside phosphorylase deficiency,,,,,DOID:5813,purine nucleoside phosphorylase deficiency,C0268125,,613179,MONDO:0013171,purine nucleoside phosphorylase deficiency,Purine-nucleoside phosphorylase deficiency | PNP deficiency | NP deficiency | Nucleoside phosphorylase deficiency | Purine nucleoside phosphorylase deficiency | PNP - Purine nucleoside phosphorylase deficiency | Deficiency of purine-nucleoside phosphorylase | NP - Nucleoside phosphorylase deficiency | Deficiency of inosine phosphorylase | Purine-nucleoside phosphorylase deficiency (disorder)
+BMGC_DS04781,BMG_DS009904,15285008,Adenylosuccinate lyase deficiency (disorder),,,,,,,C0268126,,103050,MONDO:0007068,adenylosuccinate lyase deficiency,Adenylosuccinate lyase deficiency | Succinylpurinemic autism | Succinyladenosinuria | Adenylosuccinate deficiency | Succinylpurinaemic autism | ASase - Adenylosuccinate lyase deficiency | Adenylosuccinate lyase deficiency (disorder) | Deficiency of adenylosuccinate lyase
+BMGC_DS04782,BMG_DS009907,69525003,"Hereditary orotic aciduria, type 1",,,,,,,C0268130,,,,,"Hereditary orotic aciduria, type 1 | Orotidylic pyrophosphorylase orotidylic decarboxylase deficiency | UMP synthase deficiency | OPRT AND OMP decarboxylase deficiency | Combined orotic acid phosphoribosyltransferase and orotidine - 5 - phosphate decarboxylase deficiency | Hereditary orotic aciduria type 1 | UMPS - Uridine monophosphate synthase deficiency | Uridine monophosphate synthase deficiency | Hereditary orotic aciduria, type 1 (disorder)"
+BMGC_DS04783,BMG_DS009910,43477006,"Xeroderma pigmentosum, group A",,,,,,,C0268135,,278700,MONDO:0010210,xeroderma pigmentosum group A,"Xeroderma pigmentosum, group A | Xeroderma pigmentosum, group A (disorder) | Xeroderma pigmentosum group A"
+BMGC_DS04784,BMG_DS009911,1073003,"Xeroderma pigmentosum, group B",,,,,,,C0268136,,610651,MONDO:0012531,xeroderma pigmentosum group B,"Xeroderma pigmentosum, group B | Xeroderma pigmentosum, group B (disorder) | Xeroderma pigmentosum group B"
+BMGC_DS04785,BMG_DS009912,,"Xeroderma Pigmentosum, Complementation Group D",,,,,,,C0268138,C562591,278730,MONDO:0010212,xeroderma pigmentosum group D,
+BMGC_DS04786,BMG_DS009913,,,,,,,,,C0268140,,278760,MONDO:0010215,xeroderma pigmentosum group F,
+BMGC_DS04787,BMG_DS009914,36454001,"Xeroderma pigmentosum, group G",,,,,,,C0268141,,278780,MONDO:0010216,xeroderma pigmentosum group G,"Xeroderma pigmentosum, group G | Xeroderma pigmentosum, group G (disorder) | Xeroderma pigmentosum group G"
+BMGC_DS04788,BMG_DS009918,30102006,Glucose-6-phosphate transport defect,,,,,,,C0268146,,232240;232220,MONDO:0009288,glycogen storage disease Ib,Glucose-6-phosphate transport defect | Glycogen storage disease type Ib | Glucose 6-phosphate transport defect | Glucose-6-phosphate transport defect (disorder)
+BMGC_DS04789,BMG_DS009919,40191005,"Glycogen storage disease, type IX",,,,,,,C0268147,,,,,"Glycogen storage disease, type IX | Glycogen storage disease, type IX (disorder) | Glycogen storage disease type 9"
+BMGC_DS04790,BMG_DS009921,37666005;61772003,Glycogen storage disease type X,,,,,,,C0268149,,261670,MONDO:0009865,glycogen storage disease due to phosphoglycerate mutase deficiency,Glycogen storage disease type X | GSD X | Glycogenosis due to inactive phosphorylase AND kinase | Glycogen storage disease type X (disorder) | Muscle phosphoglycerate mutase deficiency | Phosphoglucomutase deficiency | Muscle phosphoglycerate mutase deficiency (disorder) | GSD X - glycogen storage disease type X | Glycogen storage disease type X
+BMGC_DS04791,BMG_DS009922,398664009;22436005;124353000;124354006,Classical galactosemia,,,,,DOID:0111459,classic galactosemia,C0268151,,230400,MONDO:0009258,classic galactosemia,Deficiency of UTP-hexose-1-phosphate uridylyltransferase | UTP-hexose-1-phosphate uridyltransferase deficiency | Deficiency of uridine triphosphate-hexose-1-phosphate uridylyltransferase | Deficiency of uridine triphosphate-hexose-1-phosphate uridylyltransferase (disorder) | Classical galactosemia | Classical galactosaemia | Classical galactosemia (disorder) | Deficiency of galactose-1-phosphate uridylyltransferase | Deficiency of galactose-1-phosphate uridyl transferase | Deficiency of UTP-hexose-1-phosphate uridylyltransferase | Classical galactosemia | Galactose-1-phosphate uridyltransferase deficiency | UTP-hexose-1-phosphate uridyltransferase deficiency | Galactose-1-phosphate uridyl transferase deficiency | GALT | Transferase deficiency galactosaemia | Transferase deficiency galactosemia | Classical galactosaemia | Deficiency of UTP-hexose-1-phosphate uridylyltransferase (disorder) | Deficiency of uridyl transferase | Deficiency of hexose-1-phosphate uridylyltransferase | Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase | GALT deficiency | Classical galactosemia | Deficiency of galactose-1-phosphate uridyl transferase | Transferase deficiency galactosemia | Transferase deficiency galactosaemia | Classical galactosaemia | Deficiency of uridine diphosphate-glucose-hexose-1-phosphate uridylyltransferase | Deficiency of uridine diphosphate-glucose-hexose-1-phosphate uridylyltransferase (disorder)
+BMGC_DS04792,BMG_DS009923,10899004,"Classical galactosemia, homozygous Duarte-type",,,,,,,C0268152,,,,,"Classical galactosemia, homozygous Duarte-type | Classical galactosaemia, homozygous Duarte-type | Classical galactosemia, homozygous Duarte-type (disorder)"
+BMGC_DS04793,BMG_DS009926,124302001,Deficiency of galactokinase,,,,,DOID:14695,galactokinase deficiency,C0268155,,230200,MONDO:0009255,galactokinase deficiency,Deficiency of galactokinase | Galactokinase deficiency galactosemia | Galactosemia II | Galactosaemia - galactokinase deficiency | Galactokinase deficiency | Galactosemia - galactokinase deficiency | Galactokinase deficiency galactosaemia | Galactosaemia II | Deficiency of galactokinase (disorder) | GALK (galactokinase) deficiency
+BMGC_DS04794,BMG_DS009928,124300009,Deficiency of fructokinase,,,,,DOID:0111680,essential fructosuria,C0268160,,229800,MONDO:0009252,essential fructosuria,Deficiency of fructokinase | Deficiency of fructokinase (disorder)
+BMGC_DS04795,BMG_DS009930,,Pentosuria,,,,,DOID:0111258,pentosuria,C0268162,C536652,260800,MONDO:0009846,pentosuria,
+BMGC_DS04796,BMG_DS009932,65520001,"Primary hyperoxaluria, type I",,,,,DOID:0111670,primary hyperoxaluria type 1,C0268164,,259900,MONDO:0009823,primary hyperoxaluria type 1,"Primary hyperoxaluria, type I | Glycolic aciduria | Alanine-glyoxylate aminotransferase deficiency | Primary hyperoxaluria, type I (disorder) | 2-Oxoglutarate glyoxylate carboligase deficiency | Oxalosis type I | Primary hyperoxaluria type I | Alanine-glycoxylate aminotransferase deficiency"
+BMGC_DS04797,BMG_DS009933,,Primary hyperoxaluria type 2,,,,,DOID:0111671,primary hyperoxaluria type 2,C0268165,C536415,260000,MONDO:0009824,primary hyperoxaluria type 2,
+BMGC_DS04798,BMG_DS009944,,"Lactase Deficiency, Congenital",,,,,DOID:0111646,congenital lactase deficiency,C0268179,C562600,223000,MONDO:0009115,congenital lactase deficiency,
+BMGC_DS04799,BMG_DS009946,,"Lactose Intolerance, Adult Type",,,,,,,C0268181,C562601,223100,MONDO:0006065,lactose intolerance adult type,
+BMGC_DS04800,BMG_DS009950,27943000,Congenital glucose-galactose malabsorption,,,,,DOID:0070563,glucose-galactose malabsorption,C0268186,,606824,MONDO:0011731,glucose-galactose malabsorption,Congenital glucose-galactose malabsorption | Congenital glucose-galactose intolerance | Congenital glucose-galactose malabsorption (disorder)
+BMGC_DS04801,BMG_DS009951,84193000,"alpha, alpha-Trehalase deficiency",,,,,,,C0268187,,612119,MONDO:0012803,diarrhea-vomiting due to trehalase deficiency,"Trehalose intolerance | Trehalase deficiency | Alpha, alpha-trehalase deficiency | Trehalase deficiency (disorder)"
+BMGC_DS04802,BMG_DS009957,,NADH cytochrome B5 reductase deficiency,,,,,,,C0268193,C537841,250800,MONDO:0009606,methemoglobinemia due to deficiency of methemoglobin reductase,
+BMGC_DS04803,BMG_DS009958,5335002,Phosphoenolpyruvate carboxykinase deficiency,,,,,,,C0268194,C536654,,MONDO:0017320,phosphoenolpyruvate carboxykinase deficiency,Phosphoenolpyruvate carboxykinase (GTP) deficiency | Phosphoenolpyruvate carboxykinase deficiency | PEPCK - Phosphoenolpyruvate carboxykinase deficiency | Phosphoenolpyruvate carboxykinase deficiency (disorder)
+BMGC_DS04804,BMG_DS009962,33513003,Familial apolipoprotein C-II deficiency,,,,,DOID:0111418,familial apolipoprotein C-II deficiency,C0268199,,,,,Familial apolipoprotein C-II deficiency | Anapolipoproteinemia | Anapolipoproteinaemia | Familial apolipoprotein C-II deficiency (disorder) | Familial apoC-II deficiency
+BMGC_DS04805,BMG_DS009972,,Fucosidosis Type I,Fucosidosis,,,,,,C0268221,D005645,,,,
+BMGC_DS04806,BMG_DS009973,,Fucosidosis Type II,Fucosidosis,,,,,,C0268222,D005645,,,,
+BMGC_DS04807,BMG_DS009974,54954004,Aspartylglucosaminuria,Aspartylglucosaminuria,5C56.4,Disorders of sialic acid metabolism,E77.1,DOID:0050461,aspartylglucosaminuria,C0268225,D054880,208400;MTHU014368,MONDO:0008830,aspartylglucosaminuria,Aspartylglucosaminuria | Aspartylglycosaminuria | Aspartylglucosaminidase deficiency | Aspartylglucosaminuria (disorder) | Aspartylglycosylaminase deficiency
+BMGC_DS04808,BMG_DS009975,,Type I Mucolipidosis,Mucolipidoses,,,,,,C0268226,D009081,,MONDO:0017734,sialidosis,
+BMGC_DS04809,BMG_DS009976,,Neuraminidase 1 deficiency,,,,,,,C0268228,C537366,,,,
+BMGC_DS04810,BMG_DS009981,,GALACTOSIALIDOSIS,,,,,DOID:0080540,galactosialidosis,C0268233,,256540;613111,MONDO:0009737,galactosialidosis,
+BMGC_DS04811,BMG_DS009982,,Cytochrome-c Oxidase Deficiency,Cytochrome-c Oxidase Deficiency,,,,DOID:3762,cytochrome-c oxidase deficiency disease,C0268237,D030401,,MONDO:0009068,cytochrome-c oxidase deficiency disease,
+BMGC_DS04812,BMG_DS009983,19604005,Triglyceride storage disease with ichthyosis,,,,,,,C0268238,,275630,MONDO:0010155,Dorfman-Chanarin disease,Triglyceride storage disease with ichthyosis | Chanarin-Dorfman disease | Chanarin-Miranda syndrome | Ichthyosiform erythroderma with leukocyte vacuolation | Ichthyotic neutral lipid storage disease | Neutral lipid storage disease | Lipid storage myopathy AND congenital ichthyosis | Ichthyosiform erythroderma with leucocyte vacuolation | Triglyceride storage disease with ichthyosis (disorder)
+BMGC_DS04813,BMG_DS009986,,"Niemann-Pick Disease, Type A","Niemann-Pick Disease, Type A",,,,,,C0268242,D052536,257200,MONDO:0009756,Niemann-Pick disease type A,
+BMGC_DS04814,BMG_DS009987,,"Niemann-Pick Disease, Type B","Niemann-Pick Disease, Type B",,,,,,C0268243,D052537,607616,MONDO:0011871,Niemann-Pick disease type B,
+BMGC_DS04815,BMG_DS009991,,"Niemann-Pick Disease, Type D","Niemann-Pick Disease, Type C",,,,,,C0268247,D052556,,,,
+BMGC_DS04816,BMG_DS009992,,"Niemann-Pick Disease, Type E","Niemann-Pick Disease, Type B",,,,,,C0268248,D052537,,MONDO:0020384,Niemann-Pick disease type E,
+BMGC_DS04817,BMG_DS009993,,"Gaucher Disease, Type 2",Gaucher Disease,,,,,,C0268250,D005776,230900,MONDO:0009266,Gaucher disease type II,
+BMGC_DS04818,BMG_DS009994,,"Gaucher Disease, Type 3",Gaucher Disease,,,,,,C0268251,D005776,231000,MONDO:0009267,Gaucher disease type III,
+BMGC_DS04819,BMG_DS009995,,Late-Onset Globoid Cell Leukodystrophy,"Leukodystrophy, Globoid Cell",,,,,,C0268252,D007965,,MONDO:0016091,adult Krabbe disease,
+BMGC_DS04820,BMG_DS009996,,Farber Lipogranulomatosis,Farber Lipogranulomatosis,,,,DOID:0050464,Farber lipogranulomatosis,C0268255,D055577,228000,MONDO:0009218,Farber lipogranulomatosis,
+BMGC_DS04821,BMG_DS009999,,Metachromatic Leukodystrophy due to Saposin B Deficiency,,,,,,,C0268262,C562609,249900,MONDO:0009590,metachromatic leukodystrophy due to saposin B deficiency,
+BMGC_DS04822,BMG_DS010000,,Multiple Sulfatase Deficiency Disease,Multiple Sulfatase Deficiency Disease,,,,DOID:0050441,mucosulfatidosis,C0268263,D052517,272200,MONDO:0010088,mucosulfatidosis,
+BMGC_DS04823,BMG_DS010001,,"Gangliosidosis, Generalized GM1, Type 1","Gangliosidosis, GM1",,,,,,C0268271,D016537,230500,MONDO:0009260,GM1 gangliosidosis type 1,
+BMGC_DS04824,BMG_DS010002,,"Gangliosidosis, Generalized GM1, Type 2","Gangliosidosis, GM1",,,,,,C0268272,D016537,230600,MONDO:0009261,GM1 gangliosidosis type 2,
+BMGC_DS04825,BMG_DS010003,,"Gangliosidosis, Generalized GM1, Type 3","Gangliosidosis, GM1",,,,,,C0268273,D016537,230650,MONDO:0009262,GM1 gangliosidosis type 3,
+BMGC_DS04826,BMG_DS010004,,"Gangliosidoses, GM2","Gangliosidoses, GM2",,,,DOID:3321,GM2 gangliosidosis,C0268274,D020143,,MONDO:0017720,GM2 gangliosidosis,
+BMGC_DS04827,BMG_DS010005,,"Tay-Sachs Disease, AB Variant","Tay-Sachs Disease, AB Variant",,,,DOID:4795,"GM2 gangliosidosis, AB variant",C0268275,D049290,272750,MONDO:0010099,Tay-Sachs disease AB variant,
+BMGC_DS04828,BMG_DS010006,9537004,Juvenile GM2 gangliosidosis,,,,E75.09,,,C0268276,,,,,"GM>2< gangliosidosis, type 3 | Juvenile GM2 gangliosidosis (disorder) | Juvenile GM2 gangliosidosis"
+BMGC_DS04829,BMG_DS010013,,"Adrenal hyperplasia, congenital, type 5",,,,,,,C0268285,C538237,202110,MONDO:0008730,congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency,
+BMGC_DS04830,BMG_DS010018,,Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency,,,,,,,C0268292,C535978,202010,MONDO:0008729,congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency,
+BMGC_DS04831,BMG_DS010019,,,,,,,,,C0268293,,203400,MONDO:0008751,corticosterone methyloxidase type 1 deficiency,
+BMGC_DS04832,BMG_DS010020,,17-Hydroxysteroid Dehydrogenase Deficiency,,,,,,,C0268296,C537805,264300,MONDO:0009916,"46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency",
+BMGC_DS04833,BMG_DS010021,,Pseudovaginal Perineoscrotal Hypospadias,,,,,,,C0268297,C535830,264600,MONDO:0009923,"46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency",
+BMGC_DS04834,BMG_DS010022,,Reifenstein Syndrome,Androgen-Insensitivity Syndrome,,,,,,C0268301,D013734,312100;312300;307300,MONDO:0010720,partial androgen insensitivity syndrome,
+BMGC_DS04835,BMG_DS010030,74162007,Progressive intrahepatic cholestasis (disorder),,,,,DOID:0070221,progressive familial intrahepatic cholestasis,C0268312,,,MONDO:0015762,progressive familial intrahepatic cholestasis,Progressive intrahepatic cholestasis | Familial intrahepatic cholestasis | Fatal intrahepatic cholestasis | Progressive intrahepatic cholestasis (disorder) | Progressive familial intrahepatic cholestasis | PFIC - progressive familial intrahepatic cholestasis
+BMGC_DS04836,BMG_DS010032,28724005,"Cholestasis-edema syndrome, Norwegian type",,,,,DOID:6691,Aagenaes syndrome,C0268314,,214900,MONDO:0008966,Aagenaes syndrome,"Cholestasis-edema syndrome, Norwegian type | Aagenaes syndrome | Cholestasis-lymphedema syndrome | Cholestatic jaundice with hereditary lymphedema | Norwegian cholestasis | Cholestasis-lymphoedema syndrome | Cholestatic jaundice with hereditary lymphoedema | Cholestasis-oedema syndrome, Norwegian type | Cholestasis-edema syndrome, Norwegian type (disorder)"
+BMGC_DS04837,BMG_DS010035,235888006;950004,Cholestasis of pregnancy,,,,,,,C0268318,,,MONDO:0100429,intrahepatic cholestasis of pregnancy,Intrahepatic cholestasis of pregnancy | Recurrent jaundice of pregnancy | Recurrent intrahepatic cholestasis of pregnancy | Cholestasis of pregnancy | Cholestasis of pregnancy (disorder) | RICP - recurrent intrahepatic cholestasis of pregnancy | Intrahepatic cholestasis of pregnancy | Intrahepatic cholestasis of pregnancy (disorder)
+BMGC_DS04838,BMG_DS010039,59229005,Familial porphyria cutanea tarda,,,,,,,C0268323,,176100,MONDO:0008296,familial porphyria cutanea tarda,Familial porphyria cutanea tarda | Hereditary porphyria cutanea tarda | Familial porphyria cutanea tarda (disorder) | PCT (porphyria cutanea tarda) type II
+BMGC_DS04839,BMG_DS010043,64081000,Porphobilinogen synthase deficiency,,,,,,,C0268328,,612740,MONDO:0013000,porphyria due to ALA dehydratase deficiency,Porphobilinogen synthase deficiency | ALA dehydratase deficiency porphyria | ALAD deficiency | ALADH deficiency | Hereditary delta-aminolevulinic aciduria | Acute hepatic porphyria | Delta-aminolevulinate dehydrase deficiency | Delta-aminolaevulinate dehydrase deficiency | Porphobilinogen synthase deficiency (disorder) | Porphyria due to delta-aminolevulinate dehydratase deficiency | Porphyria of Doss
+BMGC_DS04840,BMG_DS010046,,Ehlers-Danlos syndrome type 1,,,,,DOID:14720,Ehlers-Danlos syndrome classic type 1,C0268335,C536194,130000,MONDO:0019567,"Ehlers-Danlos syndrome, classic type, 1",
+BMGC_DS04841,BMG_DS010047,,Ehlers-Danlos syndrome type 2,,,,,,,C0268336,C536195,130010,MONDO:0019568,"Ehlers-Danlos syndrome, classic type, 2",
+BMGC_DS04842,BMG_DS010048,30652003,"Ehlers-Danlos syndrome, type 3 (disorder)",,,,,DOID:14757,Ehlers-Danlos syndrome hypermobility type,C0268337,,130020,MONDO:0007523,"Ehlers-Danlos syndrome, hypermobility type","Ehlers-Danlos syndrome, type 3 | Benign hypermobility syndrome | Ehlers-Danlos syndrome, benign hypermobile form | Hypermobile Ehlers-Danlos syndrome (disorder) | Hypermobile Ehlers-Danlos syndrome"
+BMGC_DS04843,BMG_DS010049,,"Ehlers-Danlos Syndrome, Type IV","Ehlers-Danlos Syndrome, Type IV",,,,,,C0268338,D000094623,,MONDO:0017314,"Ehlers-Danlos syndrome, vascular type",
+BMGC_DS04844,BMG_DS010050,,,,,,,,,C0268339,,130050,MONDO:0007524,"autosomal dominant Ehlers-Danlos syndrome, vascular type",
+BMGC_DS04845,BMG_DS010051,,,,,,,DOID:14759,autosomal recessive type IV Ehlers-Danlos syndrome,C0268340,,,MONDO:0002014,"autosomal recessive Ehlers-Danlos syndrome, vascular type",
+BMGC_DS04846,BMG_DS010052,,Ehlers-Danlos syndrome type 5,,,,,DOID:0111765,X-linked cardiac valvular dysplasia,C0268341,C536197,305200,MONDO:0010586,X-linked Ehlers-Danlos syndrome,
+BMGC_DS04847,BMG_DS010053,,Ehlers-Danlos syndrome type 6,,,,,DOID:14775,brittle cornea syndrome 1,C0268342,C536198,225400,MONDO:0009242;MONDO:0016002,"Ehlers-Danlos syndrome, kyphoscoliotic type 1 | brittle cornea syndrome",
+BMGC_DS04848,BMG_DS010055,,Ehlers-Danlos syndrome 6B,,,,,,,C0268344,C536192,229200,MONDO:0024543,brittle cornea syndrome 1,
+BMGC_DS04849,BMG_DS010057,,"Ehlers-Danlos Syndrome, Type VIII",,,,,,,C0268347,C562626,,MONDO:0007527,"Ehlers-Danlos syndrome, periodontitis type",
+BMGC_DS04850,BMG_DS010060,,"Cutis Laxa, Autosomal Dominant",,,,,,,C0268350,C562627,,MONDO:0019571,autosomal dominant cutis laxa,
+BMGC_DS04851,BMG_DS010061,,,,,,,DOID:0070144,autosomal recessive cutis laxa type I,C0268351,,,MONDO:0019572,autosomal recessive cutis laxa type 1,
+BMGC_DS04852,BMG_DS010063,,,,,,,DOID:0111272,occipital horn syndrome,C0268353,,304150,MONDO:0010572,occipital horn syndrome,
+BMGC_DS04853,BMG_DS010064,,De Barsy syndrome,,,,,DOID:0070143,autosomal recessive cutis laxa type III,C0268354,C535990,,MONDO:0017569,de Barsy syndrome,
+BMGC_DS04854,BMG_DS010065,,"Cutis Laxa, Autosomal Recessive, Type IIA",,,,,,,C0268355,C562632,219200,MONDO:0018163,autosomal recessive cutis laxa type 2A,
+BMGC_DS04855,BMG_DS010068,7134007,"Osteogenesis imperfecta, dominant perinatal lethal",,,,,,,C0268358,,166210,MONDO:0008147,osteogenesis imperfecta type 2,"Osteogenesis imperfecta, dominant perinatal lethal | Osteogenesis imperfecta type II, dominant form | Neonatal lethal osteogenesis imperfecta congenita | Osteogenesis imperfecta, dominant perinatal lethal (disorder)"
+BMGC_DS04856,BMG_DS010071,385483009,Osteogenesis imperfecta type III (disorder),,,,,,,C0268362,,259420,MONDO:0009804,osteogenesis imperfecta type 3,Osteogenesis imperfecta type III (disorder) | Osteogenesis imperfecta type III
+BMGC_DS04857,BMG_DS010072,205497004,Osteogenesis imperfecta type IV (disorder),,,,,,,C0268363,,166220,MONDO:0008148,osteogenesis imperfecta type 4,"Osteogenesis imperfecta type IV | Osteogenesis imperfecta, type IV | Osteogenesis imperfecta with normal sclerae, dominant form | Osteogenesis imperfecta type IV (disorder)"
+BMGC_DS04858,BMG_DS010075,,,,,,,,,C0268368,,226500,MONDO:0009178,epidermolysis bullosa dystrophica Neurotrophica,
+BMGC_DS04859,BMG_DS010076,,,,,,,,,C0268371,,132000,MONDO:0007557,epidermolysis bullosa with congenital localized absence of skin and deformity of nails,
+BMGC_DS04860,BMG_DS010078,33662006,Adult junctional epidermolysis bullosa (disorder),,,,,,,C0268374,,226650,MONDO:0009180,"junctional epidermolysis bullosa, non-Herlitz type","Adult junctional epidermolysis bullosa | Epidermolysis bullosa junctionalis, Disentis type | Adult junctional epidermolysis bullosa (disorder)"
+BMGC_DS04861,BMG_DS010081,191397007;62793002,Pseudocholinesterase deficiency,,,,,,,C0268379,C537417,,,,Serum cholinesterase defect | Butyrylcholinesterase deficiency | Plasma cholinesterase deficiency | Suxamethonium paralysis | Serum cholinesterase deficiency | Cholinesterase deficiency | Pseudocholinesterase deficiency | Pseudocholinesterase deficiency (disorder) | Serum cholinesterase defect | Serum cholinesterase defect (disorder)
+BMGC_DS04862,BMG_DS010083,23132008;302871005,Primary amyloidosis,,,,,,,C0268381,,,MONDO:0019438,AL amyloidosis,AL amyloidosis | Amyloid light-chain amyloidosis (disorder) | Amyloid light-chain amyloidosis | Primary amyloidosis of light chain type | Primary amyloidosis | Primary amyloidosis (disorder)
+BMGC_DS04863,BMG_DS010086,,"Familial Amyloid Neuropathy, Portuguese Type","Amyloid Neuropathies, Familial",,,,,,C0268384,D028227,,MONDO:0100552,ATTRV30M amyloidosis,
+BMGC_DS04864,BMG_DS010087,,"Familial Amyloid Polyneuropathy, Jewish Type","Amyloid Neuropathies, Familial",,,,,,C0268385,D028227,,,,
+BMGC_DS04865,BMG_DS010088,,"Amyloid Polyneuropathy, Swiss Type","Amyloid Neuropathies, Familial",,,,,,C0268386,D028227,,,,
+BMGC_DS04866,BMG_DS010089,,"Amyloidosis, familial visceral",,,,,,,C0268389,C538249,105200,MONDO:0007099,familial visceral amyloidosis,
+BMGC_DS04867,BMG_DS010090,,Muckle-Wells Syndrome,Cryopyrin-Associated Periodic Syndromes,,,,DOID:0050854,Muckle-Wells syndrome,C0268390,D056587,191900,MONDO:0008633,Muckle-Wells syndrome,
+BMGC_DS04868,BMG_DS010092,,Familial Cerebral Amyloid Angiopathy,"Cerebral Amyloid Angiopathy, Familial",,,,DOID:9246,cerebral amyloid angiopathy,C0268393,D028243,,MONDO:0018591,ITM2B amyloidosis,
+BMGC_DS04869,BMG_DS010094,61985005;733729003;282834007,Primary localized cutaneous amyloidosis,,,,,,,C0268397,,,MONDO:0015301,primary cutaneous amyloidosis,Primary localized cutaneous amyloidosis | Primary localised cutaneous amyloidosis | Primary localized cutaneous amyloidosis (disorder) | Primary localized cutaneous amyloidosis (disorder) | Primary localized cutaneous amyloidosis | Primary localised cutaneous amyloidosis | Cutaneous amyloidosis | Primary cutaneous amyloidosis | Amyloidosis of dermis | Amyloidosis cutis | Primary localised cutaneous amyloidosis | Primary localized cutaneous amyloidosis | Cutaneous amyloidosis (disorder)
+BMGC_DS04870,BMG_DS010096,,"Amyloidosis, Cutaneous Bullous",,,,,,,C0268399,C562644,204900,MONDO:0008778,"amyloidosis, cutaneous bullous",
+BMGC_DS04871,BMG_DS010102,32599008,Hemodialysis-associated amyloidosis,,5D00.1,AA amyloidosis,E85.3,DOID:0080936,serum amyloid A amyloidosis,C0268405,,,MONDO:0019440,wild type ABeta2M amyloidosis,Hemodialysis-associated amyloidosis | beta-2-Microglobulin amyloidosis | Dialysis-associated amyloidosis | Beta-2 microglobulin amyloidosis | Haemodialysis-associated amyloidosis | Hemodialysis-associated amyloidosis (disorder)
+BMGC_DS04872,BMG_DS010104,16573007,Senile cardiac amyloidosis,,,,,,,C0268407,,,,,Senile cardiac amyloidosis | AS transthyretin amyloidosis | Cardiac amyloidosis | Amyloid heart muscle disease | Senile cardiac amyloidosis (disorder) | Stiff heart syndrome | Wild-type transthyretin cardiac amyloidosis
+BMGC_DS04873,BMG_DS010107,,Acid Phosphatase Deficiency,,,,,,,C0268410,C562645,200950,MONDO:0008705,lysosomal acid phosphatase deficiency,
+BMGC_DS04874,BMG_DS010108,55236002,Infantile hypophosphatasia,,,,,,,C0268412,,,,,"Infantile hypophosphatasia | Hypophosphatasia, infantile type | Congenital hypophosphatasia | Fetal hypophosphatasia | Phosphoethanolaminuria | Rathbun syndrome | Infantile hypophosphatasia (disorder) | Foetal hypophosphatasia"
+BMGC_DS04875,BMG_DS010109,20756002,Adult hypophosphatasia,,,,,,,C0268413,,,,,"Adult hypophosphatasia | Hypophosphatasia, adult type | Adult hypophosphatasia (disorder)"
+BMGC_DS04876,BMG_DS010110,9723006,Hyperphosphatasemia with bone disease,,,,,,,C0268414,,239000,MONDO:0009394,juvenile Paget disease,Hyperphosphatasemia with bone disease | Chronic congenital idiopathic hyperphosphatasemia | Familial idiopathic hyperphosphatasemia | Familial osteoectasia | Hyperostosis corticalis deformans juvenilis | Juvenile Paget disease | Osteochalasia desmalis familiaris | Osteoectasia with hyperphosphatasia | Chronic congenital idiopathic hyperphosphatasaemia | Hyperphosphatasaemia with bone disease | Familial idiopathic hyperphosphatasaemia | Hyperphosphatasemia with bone disease (disorder)
+BMGC_DS04877,BMG_DS010111,,Enterokinase Deficiency,,,,,DOID:0111667,enterokinase deficiency,C0268416,C562649,226200,MONDO:0009173,congenital enteropathy due to enteropeptidase deficiency,
+BMGC_DS04878,BMG_DS010112,65660008,Pancreatic trypsinogen deficiency,,,,,,,C0268417,,614044,MONDO:0013543,trypsinogen deficiency,Pancreatic trypsinogen deficiency | Congenital trypsinogen deficiency | Pancreatic trypsinogen deficiency (disorder)
+BMGC_DS04879,BMG_DS010113,124322002,Deficiency of glycerol kinase,,,,,,,C0268418,,307030,MONDO:0010613,inborn glycerol kinase deficiency,Deficiency of glycerol kinase | Glycerol kinase deficiency | GKD - Glycerol kinase deficiency | GK1 deficiency | Familial hyperglycerolemia | Hyperglycerolemia | Familial hyperglycerolaemia | Hyperglycerolaemia | Deficiency of glycerol kinase (disorder)
+BMGC_DS04880,BMG_DS010114,111393000;267454002;190954001,Acatalasia,Acatalasia,,,,DOID:2582,acatalasia,C0268419,D020642,614097,MONDO:0013571,acatalasia,Acatalasia | Takahara disease | Acatalasemia | Acatalasaemia | Acatalasia (disorder) | Acatalasemia | Catalase deficiency | Acatalasaemia | Acatalasemia (disorder) | Takahara disease | Acatalasia | Acatalasia | Acatalasia (disorder)
+BMGC_DS04881,BMG_DS010117,64235006,Ethanolaminosis,,,,,,,C0268423,C562651,227150,MONDO:0009199,ethanolaminosis,Ethanolaminosis | Ethanolamine kinase deficiency | Ethanolaminuria | Ethanolaminosis (disorder)
+BMGC_DS04882,BMG_DS010119,,Alstrom Syndrome,Alstrom Syndrome,,,,DOID:0050473,Alstrom syndrome,C0268425,D056769,203800,MONDO:0008763,Alstrom syndrome,
+BMGC_DS04883,BMG_DS010127,,"Renal Tubular Acidosis, Type II","Acidosis, Renal Tubular",,,,,,C0268435,D000141,179830,MONDO:0008369,proximal renal tubular acidosis,
+BMGC_DS04884,BMG_DS010128,,"Pseudohypoaldosteronism, Type I",Pseudohypoaldosteronism,,,,DOID:0060854,autosomal recessive pseudohypoaldosteronism type 1,C0268436,D011546,,MONDO:0019161,pseudohypoaldosteronism type 1,
+BMGC_DS04885,BMG_DS010132,,Acquired Nephrogenic Diabetes Insipidus,"Diabetes Insipidus, Nephrogenic",,,,,,C0268443,D018500,,,,
+BMGC_DS04886,BMG_DS010133,,"Hypokalemia, Familial",,,,,,,C0268444,C562654,241150,MONDO:0009423,"hypokalemic alkalosis, familial, with specific renal tubulopathy",
+BMGC_DS04887,BMG_DS010135,30967002,Thyrotoxic periodic paralysis,,,,,,,C0268446,,,MONDO:0019201,thyrotoxic periodic paralysis,Thyrotoxic periodic paralysis | Hashitoxic periodic paralysis | Thyrotoxic periodic paralysis (disorder)
+BMGC_DS04888,BMG_DS010137,80710001,Primary hypomagnesemia (disorder),,,,,,,C0268448,,248250,MONDO:0009550,renal hypomagnesemia 3,Primary hypomagnesemia | Primary hypomagnesaemia | Primary hypomagnesemia (disorder)
+BMGC_DS04889,BMG_DS010139,,Gitelman Syndrome,Gitelman Syndrome,,,,DOID:0050450,Gitelman syndrome,C0268450,D053579,263800,MONDO:0009904,Gitelman syndrome,
+BMGC_DS04890,BMG_DS010148,58256000,Phenylketonuria II,Phenylketonurias,,,,,,C0268465,D010661,261630,MONDO:0009862,dihydropteridine reductase deficiency,"Dihydropteridine reductase deficiency | Atypical phenylketonuria | DHPR deficiency | Hyperphenylalaninemia, type IV | Atypical PKU | Phenylketonuria II | DHPR - Dihydropteridine reductase deficiency | Hyperphenylalaninaemia, type IV | Dihydropteridine reductase deficiency (disorder)"
+BMGC_DS04891,BMG_DS010149,,"Hyperphenylalaninemia, BH4-Deficient, B",,,,,,,C0268467,C562656,,MONDO:0100184,GTP cyclohydrolase I deficiency,
+BMGC_DS04892,BMG_DS010150,,"Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency",,,,,DOID:0111168,sepiapterin reductase deficiency,C0268468,C562657,612716,MONDO:0012994,dopa-responsive dystonia due to sepiapterin reductase deficiency,
+BMGC_DS04893,BMG_DS010153,,Tryptophanuria With Dwarfism,,,,,,,C0268473,C562658,276100,MONDO:0010157,Tryptophanuria with dwarfism,
+BMGC_DS04894,BMG_DS010154,33116002;190690005,Hydroxykynureninuria,,,,,DOID:0112257,hydroxykynureninuria,C0268474,C536081,236800;MTHU074673,MONDO:0009372,encephalopathy due to hydroxykynureninuria,Hydroxykynureninuria | Hydroxykynureninuria (disorder)
+BMGC_DS04895,BMG_DS010156,59531002,Blue diaper syndrome,,,,,,,C0268478,C536239,211000,MONDO:0008877,blue diaper syndrome,Tryptophan malabsorption syndrome | Blue diaper syndrome | Tryptophan malabsorption syndrome (disorder)
+BMGC_DS04896,BMG_DS010157,,Hooft disease,,,,,,,C0268479,C535329,236300,MONDO:0009355,Hooft disease,
+BMGC_DS04897,BMG_DS010159,,,,,,,DOID:9275,tyrosinemia,C0268483,,,MONDO:0004741,tyrosinemia,
+BMGC_DS04898,BMG_DS010160,190692002;57414003,Tyrosinosis,,,,,,,C0268484,C562659,276800,MONDO:0010163,Tyrosinosis,Tyrosinosis | Tyrosinosis (disorder) | Tyrosinosis | Excessive accumulation of tyrosine in tissue | Tyrosinosis (disorder)
+BMGC_DS04899,BMG_DS010163,,Tyrosine Transaminase Deficiency Disease,Tyrosinemias,,,,,,C0268487,D020176,276600,MONDO:0010160,tyrosinemia type II,
+BMGC_DS04900,BMG_DS010165,,"Tyrosinemia, Type I",Tyrosinemias,,,,,,C0268490,D020176,276700,MONDO:0010161,tyrosinemia type I,
+BMGC_DS04901,BMG_DS010168,765146000,Oculocutaneous albinism type 1,,,,,,,C0268494,C537728,,MONDO:0018135,oculocutaneous albinism type 1,Oculocutaneous albinism type 1 (disorder) | Oculocutaneous albinism type 1 | TYR-gene related oculocutaneous albinism type 1
+BMGC_DS04902,BMG_DS010169,26336006,Oculocutaneous albinism type 2,,,,,DOID:0070096,oculocutaneous albinism type II,C0268495,C537730,203200,MONDO:0008746,oculocutaneous albinism type 2,Tyrosinase-positive oculocutaneous albinism | Tyrosinase-positive oculocutaneous albinism (disorder) | OCA2 - Tyrosinase-positive oculocutaneous albinism | Albinoidism | Oculocutaneous albinism type 2
+BMGC_DS04903,BMG_DS010174,266455006;44967007,"Ocular albinism, type II",,,,,,,C0268505,,300600,MONDO:0010371,Aland island eye disease,"Ocular albinism, type II | Forsius-Eriksson syndrome | Aland island eye disease | Forsius-Eriksson type ocular albinism | Ocular albinism, type II (disorder) | Ocular albinism, type II | Ocular albinism, type II (disorder)"
+BMGC_DS04904,BMG_DS010179,44176004,Disorder of histidine metabolism,,,,,DOID:9265,histidine metabolism disease,C0268512,,,MONDO:0019228,inborn disorder of histidine metabolism,Disorder of histidine metabolism | Disorder of histidine metabolism (disorder)
+BMGC_DS04905,BMG_DS010181,60952007,Urocanase deficiency,,,,,DOID:0112180,urocanase deficiency,C0268514,C536479,276880;MTHU037990,MONDO:0010167,urocanic aciduria,Urocanate hydratase deficiency | Urocanic aciduria | Urocanase deficiency | Urocanate hydratase deficiency (disorder)
+BMGC_DS04906,BMG_DS010188,36799008,Glutamate-cysteine ligase deficiency,,,,,,,C0268523,,,,,Glutamate-cysteine ligase deficiency | Gamma-glutamylcysteine synthetase deficiency | Gamma-glutamyl cysteine synthase deficiency | Glutamate-cysteine ligase deficiency (disorder) | Deficiency of glutamate-cysteine ligase
+BMGC_DS04907,BMG_DS010189,78586005,gamma-Glutamyltransferase deficiency,,,,,DOID:0111257,gamma-glutamyl transpeptidase deficiency,C0268524,,231950,MONDO:0009285,gamma-glutamyl transpeptidase deficiency,Gamma-glutamyl transpeptidase deficiency | Gamma-glutamyl transpeptidase deficiency (disorder) | Gamma-glutamyl transferase deficiency | Glutathionuria
+BMGC_DS04908,BMG_DS010190,,5-oxoprolinase deficiency,,,,,,,C0268525,C535322,260005,MONDO:0009825,5-oxoprolinase deficiency,
+BMGC_DS04909,BMG_DS010192,59655002;190735009,Hyperprolinemia,,,,,,,C0268528,,,MONDO:0023419,hyperprolinemia,Hyperprolinemia | Hyperprolinaemia | Hyperprolinemia (disorder) | Hyperprolinaemia | Hyperprolinemia | Hyperprolinemia (disorder)
+BMGC_DS04910,BMG_DS010193,61071003,Proline dehydrogenase deficiency,,,,,,,C0268529,,239500,MONDO:0009400,hyperprolinemia type 1,"Proline dehydrogenase deficiency | Hyperprolinemia, type I | Proline oxidase deficiency | Hyperprolinaemia, type I | Proline dehydrogenase deficiency (disorder) | Hyperprolinaemia type I | Hyperprolinemia type I"
+BMGC_DS04911,BMG_DS010194,25739007,Hydroxyprolinemia,,,,,,,C0268531,C562669,237000,MONDO:0009374,hydroxyprolinemia,Hyperhydroxyprolinemia | Hydroxyprolinemia | Hydroxyprolinaemia | Hyperhydroxyprolinaemia | Hyperhydroxyprolinemia (disorder)
+BMGC_DS04912,BMG_DS010195,360994007;124488001,Deficiency of prolidase,,,,,DOID:0111540,prolidase deficiency,C0268532,,170100,MONDO:0008221,prolidase deficiency,Deficiency of prolidase | Deficiency of Xaa-Pro dipeptidase | Deficiency of Xaa-Pro dipeptidase (disorder) | Deficiency of proline dipeptidase | Deficiency of imidodipeptidase | Deficiency of proline dipeptidase | Deficiency of proline dipeptidase (disorder)
+BMGC_DS04913,BMG_DS010199,9111008,Glucoglycinuria,,,,,,,C0268536,C562670,138070,MONDO:0007673,Glucoglycinuria,Glucoglycinuria | Glucoglycinuria (finding)
+BMGC_DS04914,BMG_DS010200,,HHH syndrome,,,,,,,C0268540,C538380,238970,MONDO:0009393,ornithine translocase deficiency,
+BMGC_DS04915,BMG_DS010201,80908008,Ornithine carbamoyltransferase deficiency,,,,,DOID:9271,ornithine carbamoyltransferase deficiency,C0268542,,311250,MONDO:0010703,ornithine carbamoyltransferase deficiency,Ornithine carbamoyltransferase deficiency | Ornithine transcarbamylase deficiency | Deficiency of citrulline phosphorylase | Ornithine transcarbamoylase deficiency | Deficiency of ornithine carbamoyltransferase | Deficiency of ornithine transcarbamylase | Ornithine carbamoyltransferase deficiency (disorder) | OCT (ornithine carbamoyltransferase) deficiency | OTC (ornithine transcarbamylase) deficiency | OTC-gene related ornithine carbamoyltransferase deficiency
+BMGC_DS04916,BMG_DS010202,57119000,"Hyperammonemia, type III",,,,,,,C0268543,,237310,MONDO:0009377,hyperammonemia due to N-acetylglutamate synthase deficiency,"Hyperammonemia, type III | N-acetylglutamate synthetase deficiency | Amino acid acetyltransferase deficiency | N-acetylglutamate transferase deficiency | Congenital AGA deficiency | NAGS deficiency | Hyperammonaemia, type III | Hyperammonemia, type III (disorder) | N-Acetylglutamate synthase deficiency | NAGS - N-Acetylglutamate synthase deficiency | NAGS-gene related hyperammonemia type III | NAGS-gene related hyperammonaemia type III"
+BMGC_DS04917,BMG_DS010205,1264112006,Late-onset citrullinemia type I,,,,,,,C0268546,,,,,Late-onset citrullinemia type I | Late-onset citrullinaemia type I | Late-onset citrullinemia type 1 | Late-onset citrullinemia type I (disorder) | Late-onset citrullinaemia type 1
+BMGC_DS04918,BMG_DS010206,,Argininosuccinic Aciduria,Argininosuccinic Aciduria,,,,DOID:14755,argininosuccinic aciduria,C0268547,D056807,207900,MONDO:0008815,argininosuccinic aciduria,
+BMGC_DS04919,BMG_DS010207,23501004,Hyperargininemia,Hyperargininemia,,,,DOID:9278,hyperargininemia,C0268548,D020162,207800,MONDO:0008814,hyperargininemia,Arginase deficiency | Argininemia | Hyperargininemia | ARGI deficiency | Argininaemia | Hyperargininaemia | Arginase deficiency (disorder) | Deficiency of arginase | ARG1-gene related arginase deficiency | Arginase 1-gene related arginase deficiency
+BMGC_DS04920,BMG_DS010209,77402005,Disorder of lysine AND/OR hydroxylysine metabolism,,,,,,,C0268552,,,MONDO:0017351,inborn disorder of lysine and hydroxylysine metabolism,Disorder of lysine AND/OR hydroxylysine metabolism | Disorder of lysine AND/OR hydroxylysine metabolism (disorder)
+BMGC_DS04921,BMG_DS010210,,Hyperlysinemias,Hyperlysinemias,,,,DOID:9274,hyperlysinemia,C0268553,D020167,238700,MONDO:0009388,hyperlysinemia,
+BMGC_DS04922,BMG_DS010212,,"Hyperlysinemia, Periodic",Hyperlysinemias,,,,,,C0268555,D020167,238750,MONDO:0009390,hyperlysinuria with hyperammonemia,
+BMGC_DS04923,BMG_DS010213,190726002;111397004,Saccharopinuria,,,,,,,C0268556,,268700,MONDO:0010005,saccharopinuria,Saccharopinuria | Saccharopinuria (disorder)
+BMGC_DS04924,BMG_DS010217,,"Hyperglycinemia, Nonketotic, Type I","Hyperglycinemia, Nonketotic",,,,,,C0268561,D020158,,,,
+BMGC_DS04925,BMG_DS010218,,"Hyperglycinemia, Nonketotic, Type II","Hyperglycinemia, Nonketotic",,,,,,C0268562,D020158,,,,
+BMGC_DS04926,BMG_DS010219,64852002,Sarcosinemia,,,,E72.59,DOID:0112307,sarcosinemia,C0268563,C537236,268900,MONDO:0010008,sarcosinemia,Sarcosine dehydrogenase deficiency | Sarcosinuria | Sarcosinemia | Hypersarcosinemia | Deficiency of the sarcosine dehydrogenase complex | Demethylation defect of N-methylglycine | Sarcosinaemia | Hypersarcosinaemia | Sarcosine dehydrogenase deficiency (disorder)
+BMGC_DS04927,BMG_DS010223,,Classic Maple Syrup Urine Disease,Maple Syrup Urine Disease,,,,,,C0268568,D008375,,MONDO:0017051,classic maple syrup urine disease,
+BMGC_DS04928,BMG_DS010224,,Intermittent Maple Syrup Urine Disease,Maple Syrup Urine Disease,,,,,,C0268569,D008375,,MONDO:0017053,intermittent maple syrup urine disease,
+BMGC_DS04929,BMG_DS010227,47719001,Valinemia,,,,,,,C0268573,C536524,277100,MONDO:0010174,Valinemia,Hypervalinemia | Valine transaminase deficiency | Valinemia | Valinaemia | Hypervalinaemia | Hypervalinemia (disorder)
+BMGC_DS04930,BMG_DS010228,,Hyperleucine-Isoleucinemia,,,,,,,C0268574,C562674,238340,MONDO:0009385,hyperleucine-Isoleucinemia,
+BMGC_DS04931,BMG_DS010229,87827003,Isovaleryl-CoA dehydrogenase deficiency,,,,,DOID:14753,isovaleric acidemia,C0268575,,243500,MONDO:0009475,isovaleric acidemia,Isovaleryl-CoA dehydrogenase deficiency | Isovaleric acidemia | Isovaleric acid CoA dehydrogenase deficiency | Isovaleric acidaemia | Isovaleric acid-CoA dehydrogenase deficiency | Isovaleryl-coenzyme A dehydrogenase deficiency | Isovaleryl-coenzyme A dehydrogenase deficiency (disorder) | IVD-gene related isovaleryl-coenzyme A dehydrogenase deficiency
+BMGC_DS04932,BMG_DS010232,69080001,Propionic acidemia,,,,E71.121,DOID:14701,propionic acidemia,C0268579,,606054,MONDO:0011628,propionic acidemia,Propionic acidemia | Propionic acidaemia | Ketotic glycinaemia | Ketotic hyperglycinaemia | Hyperglycinaemia with ketosis and leucopenia | Hyperglycinemia with ketosis and leukopenia | Ketotic glycinemia | Ketotic hyperglycinemia | Propionic acidemia (disorder) | Propionyl-CoA carboxylase deficiency | PCC - Propionyl-CoA carboxylase deficiency | Propionic aciduria
+BMGC_DS04933,BMG_DS010233,,Holocarboxylase Synthetase Deficiency,Holocarboxylase Synthetase Deficiency,,,,DOID:859,holocarboxylase synthetase deficiency,C0268581,D028922,253270,MONDO:0009666,holocarboxylase synthetase deficiency,
+BMGC_DS04934,BMG_DS010234,42393006;190727006,Methylmalonic acidemia,,,,E71.120,DOID:14749,methylmalonic acidemia,C0268583,C537358,MTHU037722,MONDO:0002012,methylmalonic acidemia,Methylmalonic acidemia | Methylmalonic acidaemia | Methylmalonic acidemia (disorder) | MMA - Methylmalonic aciduria | Disorder of amino acid metabolism: [methylmalonic acidemia] or [other specified straight-chain] | Other specified disturbance of other straight-chain amino-acid metabolism | Disorder of amino acid metabolism: [methylmalonic acidaemia] or [other specified straight-chain] | Methylmalonic acidemia | Methylmalonic acidaemia | Disorder of amino acid metabolism: [methylmalonic acidaemia] or [other specified straight-chain] (disorder)
+BMGC_DS04935,BMG_DS010238,76175005,"Glutaric aciduria, type 1",,,,,,,C0268595,,231670,MONDO:0009281,glutaryl-CoA dehydrogenase deficiency,"Glutaric aciduria, type 1 | Glutaric acidemia, type 1 | GA I | Glutaric aciduria type I | Glutaric acidaemia, type 1 | Glutaric aciduria, type 1 (disorder)"
+BMGC_DS04936,BMG_DS010239,,Multiple Acyl Coenzyme A Dehydrogenase Deficiency,Multiple Acyl Coenzyme A Dehydrogenase Deficiency,,,,DOID:0060358,multiple acyl-CoA dehydrogenase deficiency,C0268596,D054069,231680,MONDO:0009282,multiple acyl-CoA dehydrogenase deficiency,
+BMGC_DS04937,BMG_DS010243,,3-methylcrotonyl CoA carboxylase 1 deficiency,,,,,DOID:0080579,3-methylcrotonyl-CoA carboxylase 1 deficiency,C0268600,C535308,210200,MONDO:0008861,3-methylcrotonyl-CoA carboxylase 1 deficiency,
+BMGC_DS04938,BMG_DS010244,,,,,,,DOID:0070541,3-hydroxy-3-methylglutaryl-CoA lyase deficiency,C0268601,,246450,MONDO:0009520,3-hydroxy-3-methylglutaric aciduria,
+BMGC_DS04939,BMG_DS010245,4920001,Acetyl-CoA: carboxylase deficiency,,,,,,,C0268603,,613933,MONDO:0013493,acetyl-coa carboxylase deficiency,Deficiency of acetyl-CoA carboxylase | Deficiency of acetyl-coenzyme A carboxylase (disorder) | Acetyl-CoA carboxylase deficiency | Deficiency of acetyl-coenzyme A carboxylase
+BMGC_DS04940,BMG_DS010248,59761008,Glutamate formiminotransferase deficiency,,,,,DOID:0111679,glutamate formiminotransferase deficiency,C0268609,C537425,229100,MONDO:0009240,formiminoglutamic aciduria,Glutamate formiminotransferase deficiency | FIGLUria | Formiminoglutamic aciduria | Deficiency of glutamate formiminotransferase | Deficiency of glutamate formyltransferase | Glutamate formiminotransferase deficiency (disorder)
+BMGC_DS04941,BMG_DS010251,28882002,Disorder of sulfur-bearing amino acid metabolism,,,,,,,C0268613,,,,,Disorder of sulphur-bearing amino acid metabolism | Disorder of transsulfuration | Sulfuraminoacidemia | Disorder of sulfur-bearing amino acid metabolism | Disorder of transsulphuration | Sulphuraminoacidaemia | Disorder of sulphur-bearing amino acid including those due to folate and B12 disturbance | Disorder of sulfur-bearing amino acid including those due to folate and B12 disturbance | Disorder of sulfur-bearing amino acid metabolism (disorder)
+BMGC_DS04942,BMG_DS010253,6885006,Gamma-cystathionase deficiency,,,,,DOID:0090142,cystathioninuria,C0268616,C535408,,,,Cystathionine gamma-lyase deficiency | Gamma-cystathionase deficiency | Cystathionine gamma-lyase deficiency (disorder) | Deficiency of cystine desulphydrase | Deficiency of cysteine desulphydrase | Deficiency of cysteine desulfhydrase | Deficiency of cystine desulfhydrase | Deficiency of homoserine deaminase | Deficiency of cystathionase
+BMGC_DS04943,BMG_DS010254,52311001,Homocystinemia,,,,,,,C0268617,,,,,Homocystinemia | Homocystinaemia | Homocystinemia (disorder)
+BMGC_DS04944,BMG_DS010257,267420003;57835009,Hepatic methionine adenosyltransferase deficiency,,,,,,,C0268621,,250850,MONDO:0009607,methionine adenosyltransferase deficiency,Hepatic methionine adenosyltransferase deficiency | Hepatic methionine adenosyltransferase deficiency (disorder) | Hepatic methionine adenosyltransferase deficiency | MAT deficiency | Methionine adenosyltransferase deficiency | Hepatic methionine adenosyltransferase deficiency (disorder)
+BMGC_DS04945,BMG_DS010258,,Methionine Malabsorption Syndrome,,,,,,,C0268622,C562682,250900,MONDO:0009608,methionine malabsorption syndrome,
+BMGC_DS04946,BMG_DS010259,,"Tyrosinemia, Type III",Tyrosinemias,,,,,,C0268623,D020176,276710,MONDO:0010162,tyrosinemia type III,
+BMGC_DS04947,BMG_DS010260,367368009;237935000,Sulfite oxidase deficiency,,,,E72.19,DOID:0111270,isolated sulfite oxidase deficiency,C0268624,C538141,272300;MTHU058999,MONDO:0010089,isolated sulfite oxidase deficiency,Sulfite oxidase deficiency | Sulphite oxidase deficiency | Sulfite oxidase deficiency (disorder) | Sulfite oxidase deficiency | Sulphite oxidase deficiency | Sulphite oxidase deficiency (disorder)
+BMGC_DS04948,BMG_DS010261,22830006,Juvenile nephropathic cystinosis (disorder),,,,,,,C0268626,,219900,MONDO:0009066,juvenile nephropathic cystinosis,"Juvenile nephropathic cystinosis | Adolescent cystinosis | Intermediate cystinosis | Late-onset cystinosis | Cystinosis, type II | Juvenile cystinosis | Juvenile nephropathic cystinosis (disorder)"
+BMGC_DS04949,BMG_DS010263,2359002,Hyper-beta-alaninemia,,,,,,,C0268630,,237400,MONDO:0009378,hyper-beta-alaninemia,Hyper-beta-alaninemia | Hyperalaninemia | Hyperalaninaemia | Hyper-beta-alaninaemia | Hyper-beta-alaninemia (disorder)
+BMGC_DS04950,BMG_DS010264,,succinic semialdehyde dehydrogenase deficiency,,,,,DOID:0060175,succinic semialdehyde dehydrogenase deficiency,C0268631,C535803,271980,MONDO:0010083,succinic semialdehyde dehydrogenase deficiency,
+BMGC_DS04951,BMG_DS010265,237942000;274616003,Homocarnosinosis,,,,,DOID:0060177,homocarnosinosis,C0268632,C535328,236130,MONDO:0009351,homocarnosinosis,Homocarnosinosis | Homocarnosinosis (disorder) | Homocarnosinosis | Serum carnosinase deficiency | Homocarnosinosis (disorder)
+BMGC_DS04952,BMG_DS010266,190729009;39929009,Disorder of fatty acid metabolism,,,,,,,C0268634,,,MONDO:0037858,inherited fatty acid metabolism disorder,Disorder of fatty acid metabolism | Disorder of fatty acid metabolism (disorder) | Disorder of fatty acid metabolism | Disorders of fatty-acid metabolism | Disorder of fat oxidation | Disorder of fatty acid metabolism (disorder)
+BMGC_DS04953,BMG_DS010272,,Histidinuria renal tubular defect,,,,,,,C0268642,C538321,235830,MONDO:0009346,histidinuria due to a renal tubular defect,
+BMGC_DS04954,BMG_DS010277,,Lysinuric Protein Intolerance,,,,,DOID:0060439,lysinuric protein intolerance,C0268647,C562687,222700,MONDO:0009109,lysinuric protein intolerance,
+BMGC_DS04955,BMG_DS010282,84121007,Iminoglycinuria,,,,,DOID:0112265,iminoglycinuria,C0268654,C536285,MTHU056935;242600,MONDO:0009448,iminoglycinuria,Iminoglycinuria | Iminoglycinuria (disorder)
+BMGC_DS04956,BMG_DS010294,67360000,Wet beriberi,,,,E51.12,DOID:0070317,wet beriberi,C0268669,,,MONDO:0024183,wet beriberi,Wet beriberi | Cardiovascular beriberi | Wet beriberi (disorder)
+BMGC_DS04957,BMG_DS010295,71021002;79389008,Dry beriberi,,,,E51.11,DOID:0070318,dry beriberi,C0268670,,,MONDO:0024182,dry beriberi,Dry beriberi | Dry beriberi (disorder) | Beriberi neuropathy | Thiamine deficiency neuropathy | Vitamin B>1< deficiency neuropathy | Neuropathic beriberi | Neuropathy due to vitamin B1 deficiency | Polyneuropathy in beriberi | Beriberi neuropathy (disorder)
+BMGC_DS04958,BMG_DS010302,413652008,Biotin deficiency,,5B7Z,Unspecified undernutrition,E53.8,DOID:0050810,biotin deficiency,C0268680,C531633,,,,Biotin deficiency (disorder) | Biotin deficiency | Deficiency of biotin
+BMGC_DS04959,BMG_DS010307,67049004,"Vitamin D-dependent rickets, type 1",,,,,,,C0268689,,,MONDO:0009924,"vitamin D-dependent rickets, type 1","Vitamin D-dependent rickets, type 1 | Calcidiol 1-monooxygenase defect | Pseudo-vitamin-D-deficient rickets | Pseudodeficiency rickets | Pseudovitamin D-resistant rickets | PDDR - Pseudovitamin D deficiency rickets | 25-Hydroxycholecalciferol-1-hydroxylase deficiency | Vitamin D-dependent rickets type I | VDDR I - Vitamin D-dependent rickets type I | Pseudovitamin D deficiency rickets | Vitamin D-dependent rickets, type 1 (disorder) | 1-alpha-hydroxylase deficiency"
+BMGC_DS04960,BMG_DS010316,11659006,Uremic neuropathy,,,,,DOID:4675,uremic neuropathy,C0268708,,,MONDO:0003084,uremic neuropathy,Uremic neuropathy | Uraemic neuropathy | Uremic neuropathy (disorder)
+BMGC_DS04961,BMG_DS010328,23754003;197766000,Calculous pyelonephritis,,,,N20,,,C0268722,,,,,Calculous pyelonephritis | Pyelonephritis due to kidney stone | Pyelonephritis due to kidney stone (disorder) | Calculous pyelonephritis | Calculous pyelonephritis (disorder)
+BMGC_DS04962,BMG_DS010333,76910007,Renal glomerular disease,,,,,,,C0268731,,,,,Renal glomerular disease | Renal glomerular syndrome | Renal glomerular disorder | Renal glomerular disease (disorder)
+BMGC_DS04963,BMG_DS010336,58574008,Acute nephropathy,,,,,,,C0268734,,,,,Acute nephropathy | Acute nephropathy (disorder) | AKD - acute kidney disease
+BMGC_DS04964,BMG_DS010342,,"Membranoproliferative Glomerulonephritis, Type I","Glomerulonephritis, Membranoproliferative",,,,,,C0268742,D015432,,,,
+BMGC_DS04965,BMG_DS010343,,"Membranoproliferative Glomerulonephritis, Type II","Glomerulonephritis, Membranoproliferative",,,,,,C0268743,D015432,,MONDO:0019736,dense deposit disease,
+BMGC_DS04966,BMG_DS010347,111406002,Diffuse mesangial sclerosis (disorder),,,,,,,C0268747,,,,,Diffuse mesangial sclerosis | Diffuse mesangial sclerosis (disorder)
+BMGC_DS04967,BMG_DS010382,16934004,Renal vascular disorder,,,,,DOID:2388,renal artery disease,C0268790,,,,,Renal vascular disorder | Vascular disorder of kidney | Renal vascular disease | Renal vascular disorder (disorder)
+BMGC_DS04968,BMG_DS010391,105999006,Acquired renal cystic disease,,,,,DOID:9621,non-congenital cyst of kidney,C0268799,,,MONDO:0004840,non-congenital cyst of kidney,Acquired renal cystic disease | Acquired renal cystic disease (disorder) | Acquired renal cyst
+BMGC_DS04969,BMG_DS010402,,Dipsogenic Diabetes Insipidus,,,,,DOID:0081058,dipsogenic diabetes insipidus,C0268813,C548013,,MONDO:0022993,dipsogenic diabetes insipidus,
+BMGC_DS04970,BMG_DS010408,4009004,Lower urinary tract infectious disease,,,,,,,C0268821,,,,,Lower urinary tract infectious disease | Lower urinary tract infection | UTI - Lower urinary tract infection | Lower urinary tract infectious disease (disorder)
+BMGC_DS04971,BMG_DS010421,72815004,Cystitis glandularis,,,,,DOID:2392,glandular cystitis,C0268837,,,MONDO:0002287,glandular cystitis,Cystitis glandularis | Cystitis glandularis (disorder)
+BMGC_DS04972,BMG_DS010424,,Overactive Detrusor,"Urinary Bladder, Overactive",,,,,,C0268849,D053201,,,,
+BMGC_DS04973,BMG_DS010531,32608004,Fibrosis of corpus cavernosum,,,,,,,C0269014,,,,,Fibrosis of corpus cavernosum | Fibrosis of corpus cavernosum (disorder)
+BMGC_DS04974,BMG_DS010545,,Female acute pelvic peritonitis,,GA05.2,"Female pelvic peritonitis, unspecified",N73.3,DOID:9978,acute female pelvic peritonitis,C0269032,,,MONDO:0004940,acute female pelvic peritonitis,
+BMGC_DS04975,BMG_DS010551,8912009,Acute salpingitis,,,,N70.01,DOID:10973,acute salpingitis,C0269038,,,MONDO:0001173,acute salpingitis,Acute salpingitis | Acute salpingitis (disorder)
+BMGC_DS04976,BMG_DS010553,55551005,Chronic salpingitis,,,,N70.11,DOID:5731,chronic salpingitis,C0269041,,,MONDO:0003617,chronic salpingitis,Chronic salpingitis | Chronic salpingitis (disorder)
+BMGC_DS04977,BMG_DS010555,36742000,Salpingitis isthmica nodosa,,,,,DOID:5730,salpingitis isthmica nodosa,C0269043,,,MONDO:0003616,salpingitis isthmica nodosa,Salpingitis isthmica nodosa | Adenosis of fallopian tube | Adenosalpingitis | Salpingitis isthmica nodosa (disorder)
+BMGC_DS04978,BMG_DS010557,28783002,Inflammatory disease of the uterus,,,,,DOID:13736,uterine inflammatory disease,C0269047,,,MONDO:0001786,uterine inflammatory disease,Inflammatory disease of the uterus | Inflammatory disease of the uterus (disorder)
+BMGC_DS04979,BMG_DS010560,88027004,Endomyometritis,Endometritis,,,,,,C0269050,D004716,,MONDO:0042451,endomyometritis,Endomyometritis | Endomyometritis (disorder)
+BMGC_DS04980,BMG_DS010569,19272000,Acute cervicitis,,,,,DOID:10616,acute cervicitis,C0269061,,,MONDO:0001081,acute cervicitis,Acute cervicitis | Acute cervicitis (disorder)
+BMGC_DS04981,BMG_DS010570,56728002;198210003,Chronic cervicitis,,,,,DOID:1513,chronic cervicitis,C0269062,,,MONDO:0002030,chronic cervicitis,Chronic cervicitis | Chronic cervicitis (disorder)
+BMGC_DS04982,BMG_DS010605,55850004,Endosalpingiosis,,,,,DOID:11427,endosalpingiosis,C0269106,,,MONDO:0001283,endosalpingiosis,Endosalpingiosis | Endosalpingiosis (disorder)
+BMGC_DS04983,BMG_DS010606,61640006,Endometriosis of cervix,,,,,DOID:361,cervix endometriosis,C0269107,,,MONDO:0002706,cervix endometriosis,Endometriosis of cervix | Endometriosis of cervix (disorder)
+BMGC_DS04984,BMG_DS010647,,,,,,,DOID:9043,uterine cervix leukoplakia,C0269194,,,MONDO:0004702,uterine cervix leukoplakia,
+BMGC_DS04985,BMG_DS010694,,,,,,,,,C0269269,,163600,MONDO:0008100,nipples inverted,
+BMGC_DS04986,BMG_DS010821,,,,,,,,,C0269658,,,MONDO:0001072,mild pre-eclampsia,
+BMGC_DS04987,BMG_DS010832,,Pruritic urticarial papules plaques of pregnancy,,,,,,,C0269680,C535817,178995,MONDO:0008353,pruritic urticarial papules and plaques of pregnancy,
+BMGC_DS04988,BMG_DS010900,200179002;22399000,Puerperal endometritis,,,,,,,C0269932,,,,,Puerperal endometritis | Puerperal endometritis (disorder) | Puerperal endometritis | Puerperal endometritis (disorder) | Postpartum endometritis
+BMGC_DS04989,BMG_DS010954,,,,,,,DOID:424,pulmonary immaturity,C0270163,,,MONDO:0002929,pulmonary immaturity,
+BMGC_DS04990,BMG_DS010968,157135006;359007;268880009;206433007,Kernicterus due to isoimmunization,,KA86,Neonatal kernicterus,P57.0,DOID:12043,kernicterus due to isoimmunization,C0270204,,,MONDO:0006567,kernicterus due to isoimmunization,Kernicterus - due to isoimm. | Kernicterus | Kernicterus (& [due to isoimmunization]) | Kernicterus (& [due to isoimmunisation]) | Kernicterus due to isoimmunisation | Kernicterus due to isoimmunization | Kernicterus (& [due to isoimmunisation]) (disorder) | Kernicterus due to isoimmunization | Kernicterus due to isoimmunisation | Kernicterus due to isoimmunization (disorder) | Kernicterus (& [due to isoimmunization]) | Kernicterus (& [due to isoimmunisation]) | Kernicterus due to isoimmunization | Kernicterus due to isoimmunisation | Kernicterus | Kernicterus - due to isoimm. | Kernicterus (& [due to isoimmunisation]) (disorder) | Kernicterus due to isoimmunisation | Kernicterus due to isoimmunization | Kernicterus due to isoimmunization (disorder)
+BMGC_DS04991,BMG_DS010972,47444008,Lucey-Driscoll syndrome (disorder),,,,,,,C0270210,,237900,MONDO:0009383,transient familial neonatal hyperbilirubinemia,Lucey-Driscoll syndrome | Transient familial neonatal hyperbilirubinaemia | Transient familial neonatal hyperbilirubinemia | Lucey-Driscoll syndrome (disorder)
+BMGC_DS04992,BMG_DS010980,,"Tetany, Neonatal",Tetany,,,,,,C0270224,D013746,,,,
+BMGC_DS04993,BMG_DS011013,,,,,,,,,C0270327,,,MONDO:0000022,nocturnal enuresis,
+BMGC_DS04994,BMG_DS011014,,,,,,,DOID:1229,paranoid schizophrenia,C0270398,,,,,
+BMGC_DS04995,BMG_DS011016,,,,,,,DOID:14320,generalized anxiety disorder,C0270549,,,MONDO:0001942,generalized anxiety disorder,
+BMGC_DS04996,BMG_DS011019,22811006,Leukoencephalopathy,Leukoencephalopathies,,,,,,C0270612,D056784,MTHU001673,,,Leukoencephalopathy | Leukoencephalopathy (disorder) | Leucoencephalopathy
+BMGC_DS04997,BMG_DS011027,,"Myelitis, Acute Transverse","Myelitis, Transverse",,,,,,C0270627,D009188,,MONDO:0015342,acute transverse myelitis,
+BMGC_DS04998,BMG_DS011029,,Epidural Abscess,Epidural Abscess,,,,DOID:11387,epidural abscess,C0270629,D020802,,MONDO:0005752,epidural abscess,
+BMGC_DS04999,BMG_DS011034,,Cavernous Sinus Thrombophlebitis,Cavernous Sinus Thrombosis,,,,,,C0270638,D020226,,,,
+BMGC_DS05000,BMG_DS011035,,Lateral Sinus Thrombosis,Lateral Sinus Thrombosis,,,,DOID:3574,lateral sinus thrombosis,C0270639,D020227,,MONDO:0002693,lateral sinus thrombosis,
+BMGC_DS05001,BMG_DS011087,,,,,,,DOID:2510,Kluver-Bucy syndrome,C0270707,,,MONDO:0005817,Kluver-Bucy syndrome,
+BMGC_DS05002,BMG_DS011093,,"Degenerative Diseases, Central Nervous System",Neurodegenerative Diseases,,,,,,C0270715,D019636,,,,
+BMGC_DS05003,BMG_DS011097,,Hydrocephalus Ex-Vacuo,Hydrocephalus,,,,,,C0270720,D006849,,,,
+BMGC_DS05004,BMG_DS011101,,Infantile Neuroaxonal Dystrophy,Neuroaxonal Dystrophies,,,,,,C0270724,D019150,256600,MONDO:0024457,neurodegeneration with brain iron accumulation 2A,
+BMGC_DS05005,BMG_DS011103,,Alexander Disease,Alexander Disease,,,,DOID:4252,Alexander disease,C0270726,D038261,203450,MONDO:0008752,Alexander disease,
+BMGC_DS05006,BMG_DS011105,,Striatonigral Degeneration,Striatonigral Degeneration,,,,DOID:4751,striatonigral degeneration,C0270733,D020955,,MONDO:0003122,striatonigral degeneration,
+BMGC_DS05007,BMG_DS011108,,Essential Tremor,Essential Tremor,,,,DOID:4990,essential tremor,C0270736,D020329,,MONDO:0003233,essential tremor,
+BMGC_DS05008,BMG_DS011119,,Marie Cerebellar Ataxia,Spinocerebellar Degenerations,,,,,,C0270749,D013132,,MONDO:0100310,hereditary cerebellar ataxia,
+BMGC_DS05009,BMG_DS011124,,Corticostriatal-Spinal Degeneration,Spinocerebellar Degenerations,,,,,,C0270755,D013132,,,,
+BMGC_DS05010,BMG_DS011132,,Familial Motor Neuron Disease,Motor Neuron Disease,,,,,,C0270763,D016472,,MONDO:0024257,hereditary motor neuron disease,
+BMGC_DS05011,BMG_DS011133,,"Motor Neuron Disease, Lower",Motor Neuron Disease,,,,,,C0270764,D016472,,,,
+BMGC_DS05012,BMG_DS011134,,Myelopathic Muscular Atrophy,"Muscular Atrophy, Spinal",,,,,,C0270765,D009134,,,,
+BMGC_DS05013,BMG_DS011148,,Binswanger Disease,"Dementia, Vascular",,,,,,C0270786,D015140,,,,
+BMGC_DS05014,BMG_DS011165,,Monoplegic Cerebral Palsy,Cerebral Palsy,,,,,,C0270807,D002547,,MONDO:0022700,cerebral palsy spastic monoplegic,
+BMGC_DS05015,BMG_DS011168,,Peroneal Nerve Paralysis,Peroneal Neuropathies,,,,DOID:6925,peroneal nerve paralysis,C0270810,D020427,,MONDO:0006903,peroneal nerve paralysis,
+BMGC_DS05016,BMG_DS011173,,"Reflex Epilepsy, Cursive (Running)","Epilepsy, Reflex",,,,,,C0270819,D020195,,,,
+BMGC_DS05017,BMG_DS011174,,Gelastic Epilepsy,"Epilepsies, Partial",,,,,,C0270820,D004828,,,,
+BMGC_DS05018,BMG_DS011177,,,,,,,DOID:11832,visual epilepsy,C0270824,,,MONDO:0001386,visual epilepsy,
+BMGC_DS05019,BMG_DS011182,407675009,Focal onset impaired awareness epileptic seizure,,,,,,,C0270834,,,,,Focal onset impaired awareness seizure | FIAS - focal impaired awareness seizure | Focal onset impaired awareness epileptic seizure | Focal-onset impaired awareness epileptic seizure | Focal onset impaired awareness epileptic seizure (finding) | Focal impaired awareness seizure
+BMGC_DS05020,BMG_DS011183,20544001,"Secondarily generalized seizures, NOS",,,,,,,C0270838,,,,,Secondarily generalized seizures | Secondarily generalised seizures | Secondarily generalized seizures (finding)
+BMGC_DS05021,BMG_DS011184,,Tonic Seizures,Seizures,,,,,,C0270844,D012640,,,,
+BMGC_DS05022,BMG_DS011185,42365007;246554004;365883006,Atonic seizure,,,,,,,C0270846,,,,,Atonic seizures | Atonic seizure | Atonic seizure (disorder) | Atonic seizure | Atonic seizure (finding) | Atonic seizure - finding | Atonic seizure | Finding of atonic seizure (finding)
+BMGC_DS05023,BMG_DS011186,,"Benign Focal Epilepsy, Childhood","Epilepsies, Partial",,,,,,C0270847,D004828,,,,
+BMGC_DS05024,BMG_DS011187,111498005,Extratemporal epilepsy,,,,,DOID:2544,extratemporal epilepsy,C0270849,,,MONDO:0002338,extratemporal epilepsy,Extratemporal epilepsy | Extratemporal epilepsy (disorder)
+BMGC_DS05025,BMG_DS011188,36803009,Idiopathic generalized epilepsy,,,,,,,C0270850,,600669;MTHU076671,MONDO:0005579,idiopathic generalized epilepsy,Idiopathic generalized epilepsy | Idiopathic generalised epilepsy | Idiopathic generalized epilepsy (disorder) | IGE - idiopathic generalized epilepsy | IGE - idiopathic generalised epilepsy
+BMGC_DS05026,BMG_DS011189,,,,,,,DOID:14264,benign neonatal seizures,C0270851,,,,,
+BMGC_DS05027,BMG_DS011190,,Juvenile Myoclonic Epilepsy,"Myoclonic Epilepsy, Juvenile",,,,DOID:4890,juvenile myoclonic epilepsy,C0270853,D020190,254770;606904,MONDO:0009696,juvenile myoclonic epilepsy,
+BMGC_DS05028,BMG_DS011191,,Symptomatic Generalized Epilepsy,"Epilepsy, Generalized",,,,,,C0270854,D004829,,,,
+BMGC_DS05029,BMG_DS011192,44423001,Early myoclonic encephalopathy,,,,,,,C0270855,,,MONDO:0016022,early myoclonic encephalopathy,Early myoclonic encephalopathy | Early myoclonic encephalopathy (disorder) | Symptomatic early myoclonic encephalopathy
+BMGC_DS05030,BMG_DS011193,,"Epilepsy, Reflex","Epilepsy, Reflex",,,,DOID:2548,reflex epilepsy,C0270857,D020195,,MONDO:0017768,reflex epilepsy,
+BMGC_DS05031,BMG_DS011194,,Abdominal Migraine,Migraine Disorders,,,,,,C0270858,D008881,,,,
+BMGC_DS05032,BMG_DS011196,,Basilar-Type Migraine,Migraine with Aura,,,,,,C0270860,D020325,,MONDO:0043219,migraine with brainstem aura,
+BMGC_DS05033,BMG_DS011198,59292006,Hemiplegic migraine,,,,G43.4,,,C0270862,,,,,Hemiplegic migraine | Hemiplegic migraine (disorder)
+BMGC_DS05034,BMG_DS011204,,Facial Myokymia,Facial Nerve Diseases,,,,,,C0270871,D005155,,MONDO:0016373,isolated facial myokymia,
+BMGC_DS05035,BMG_DS011208,,Facial Nerve Motor Disorders,Facial Nerve Diseases,,,,,,C0270876,D005155,,,,
+BMGC_DS05036,BMG_DS011209,,Facial Nerve Sensory Disorders,Facial Nerve Diseases,,,,,,C0270877,D005155,,,,
+BMGC_DS05037,BMG_DS011230,399107008,Common peroneal nerve lesion (disorder),,,,,DOID:12527,common peroneal nerve lesion,C0270909,,,MONDO:0001542,common peroneal nerve lesion,Common peroneal nerve lesion (disorder) | Common peroneal nerve lesion | Lateral popliteal nerve lesion | Lesion of lateral popliteal nerve | Lesion of common peroneal nerve
+BMGC_DS05038,BMG_DS011232,,,,,,,,,C0270911,,118220,MONDO:0007309,Charcot-Marie-Tooth disease type 1A,
+BMGC_DS05039,BMG_DS011233,,,,,,,,,C0270912,,118200,MONDO:0007307,Charcot-Marie-Tooth disease type 1B,
+BMGC_DS05040,BMG_DS011234,,"Charcot-Marie-Tooth disease, Type 1C",,,,,DOID:0110151,Charcot-Marie-Tooth disease type 1C,C0270913,C537984,601098,MONDO:0010995,Charcot-Marie-Tooth disease type 1C,
+BMGC_DS05041,BMG_DS011235,,Hereditary Motor and Sensory-Neuropathy Type II,Charcot-Marie-Tooth Disease,,,,DOID:0070161,hereditary sensory and autonomic neuropathy type 2,C0270914,D002607,,MONDO:0018993,Charcot-Marie-Tooth disease type 2,
+BMGC_DS05042,BMG_DS011237,60703000,Axonal neuropathy,,,,,DOID:7319,axonal neuropathy,C0270921,,MTHU003516,,,Axonal neuropathy | Axonal neuropathy (disorder)
+BMGC_DS05043,BMG_DS011238,23414001,Peripheral demyelinating neuropathy,,,,,DOID:5214,demyelinating polyneuropathy,C0270922,,MTHU036239,MONDO:0003334,demyelinating polyneuropathy,Demyelinating polyneuropathy | Peripheral demyelinating neuropathy | Peripheral demyelinating neuropathy (disorder)
+BMGC_DS05044,BMG_DS011244,,Paraneoplastic Polyneuropathy,Paraneoplastic Polyneuropathy,,,,DOID:8681,paraneoplastic polyneuropathy,C0270932,D020364,,MONDO:0006888,paraneoplastic polyneuropathy,
+BMGC_DS05045,BMG_DS011259,,"Muscular Dystrophy, Oculopharyngeal","Muscular Dystrophy, Oculopharyngeal",,,,DOID:11719,oculopharyngeal muscular dystrophy,C0270952,D039141,,MONDO:0008116,oculopharyngeal muscular dystrophy,
+BMGC_DS05046,BMG_DS011264,,Myotonia Levior,Myotonia Congenita,,,,,,C0270959,D009224,,MONDO:0009710,Thomsen and Becker disease,
+BMGC_DS05047,BMG_DS011265,18148005,Congenital myopathy (disorder),,,,,,,C0270960,,,MONDO:0019952,congenital myopathy,Congenital myopathy | Congenital myopathy (disorder)
+BMGC_DS05048,BMG_DS011267,55133004,Multi-core congenital myopathy,,,,,,,C0270962,,,MONDO:0018948,multiminicore myopathy,Multi-core congenital myopathy | Multi-core disease | Multi-core congenital myopathy (disorder) | Minicore disease | Multicore disease | Multiminicore disease | Multi-minicore disease
+BMGC_DS05049,BMG_DS011272,,Limb-girdle muscular dystrophy type 2H,,,,,,,C0270968,C535897,254110,MONDO:0009683,autosomal recessive limb-girdle muscular dystrophy type 2H,
+BMGC_DS05050,BMG_DS011273,34513009,Zebra body myopathy,,,,,,,C0270969,,,MONDO:0019949,zebra body myopathy,Zebra body myopathy | Zebra body myopathy (disorder)
+BMGC_DS05051,BMG_DS011274,42779002,Reducing-body myopathy,,,,,,,C0270970,,,MONDO:0019948,reducing body myopathy,Reducing-body myopathy | Reducing-body myopathy (disorder)
+BMGC_DS05052,BMG_DS011276,,Cornelia De Lange Syndrome,De Lange Syndrome,,,,DOID:11725,Cornelia de Lange syndrome,C0270972,D003635,,MONDO:0016033,Cornelia de Lange syndrome,
+BMGC_DS05053,BMG_DS011293,25277000,Siderosis of eye,,,,H44.32,DOID:11754,siderosis of eye,C0271001,,,MONDO:0001355,ocular siderosis,Siderosis of eye | Ocular siderosis | Siderosis of eye (disorder)
+BMGC_DS05054,BMG_DS011315,37231002,Macular retinal edema,,,,,DOID:4449,macular retinal edema,C0271051,,,MONDO:0003005,macular retinal edema,Macular retinal edema | Macular oedema | Macular retinal oedema | Macular edema | Macular retinal edema (disorder)
+BMGC_DS05055,BMG_DS011330,,Eales disease,,,,H35.06,,,C0271073,C538011,,MONDO:0018460,Eales disease,
+BMGC_DS05056,BMG_DS011335,65593009,Partial occlusion of retinal vein,,,,,DOID:1726,partial of retinal vein occlusion,C0271080,,,MONDO:0002088,partial retinal vein occlusion,Partial occlusion of retinal vein | Partial occlusion of retinal vein (disorder)
+BMGC_DS05057,BMG_DS011337,,,,,,,,,C0271083,,,MONDO:0100114,dry age related macular degeneration,
+BMGC_DS05058,BMG_DS011338,11290001;414173003,Exudative age-related macular degeneration,,,,H35.32,DOID:10873,Kuhnt-Junius degeneration,C0271084,,,,,Kuhnt-Junius degeneration | Disciform senile macular retinal degeneration | Exudative senile macular retinal degeneration | Junius-Kuhnt degeneration | Exudative age-related macular degeneration | Disciform macular degeneration | Wet senile macular retinal degeneration | Wet senile macular degeneration | Subretinal neovascularisation of macula | Subretinal neovascularization of macula | Kuhnt-Junius degeneration (disorder) | Exudative age-related macular degeneration (disorder) | Exudative age-related macular degeneration | Exudative senile macular retinal degeneration | Neovascular age-related macular degeneration | Wet senile macular degeneration | Subretinal neovascularization of macula | Subretinal neovascularisation of macula | EMD - Exudative macular degeneration
+BMGC_DS05059,BMG_DS011340,193389005;44115007,Toxic maculopathy,,,,H35.38,DOID:9867,toxic maculopathy,C0271086,,,MONDO:0004904,toxic maculopathy,Toxic maculopathy | Toxic maculopathy (disorder)
+BMGC_DS05060,BMG_DS011344,,"Retinoschisis, Juvenile, X-Linked",Retinoschisis,,,,,,C0271091,D041441,,,,
+BMGC_DS05061,BMG_DS011345,193404003;267613004,Progressive cone dystrophy (without rod involvement),,,,,,,C0271092,,,,,Progressive retinal dystrophy: [cone (without rod involvement)] or [rod] | Progressive cone dystrophy (without rod involvement) | Progressive rod dystrophy | Progressive retinal dystrophy: [cone (without rod involvement)] or [rod] (disorder) | Progressive cone dystrophy (without rod involvement) | Progressive cone dystrophy (without rod involvement) (disorder)
+BMGC_DS05062,BMG_DS011346,70099003;193405002;193407005,Stargardt's disease,,,,H35.53,,,C0271093,,,MONDO:0019353,Stargardt disease,Stargardt's disease | Familial juvenile macular degeneration syndrome | Stargardt's disease (disorder) | Stargardt disease | Stargardt's disease | Stargardt's disease (disorder)
+BMGC_DS05063,BMG_DS011348,,Usher Syndrome,Usher Syndromes,,,,DOID:0110827;DOID:0110828;DOID:0050439,Usher syndrome | Usher syndrome type 2 | Usher syndrome type 3,C0271097,D052245,,MONDO:0019501,Usher syndrome,
+BMGC_DS05064,BMG_DS011349,68575007,Disorder of ciliary body,,,,,DOID:4353,ciliary body disease,C0271100,,,MONDO:0002970,ciliary body disorder,Disorder of ciliary body | Disorder of ciliary body (disorder)
+BMGC_DS05065,BMG_DS011368,,,,,,,,,C0271130,,178900,MONDO:0008352,"pupillary membrane, persistence of",
+BMGC_DS05066,BMG_DS011369,,Occluded Pupils,Pupil Disorders,,,,,,C0271131,D011681,,,,
+BMGC_DS05067,BMG_DS011377,,Secondary Open Angle Glaucoma,"Glaucoma, Open-Angle",,,,,,C0271148,D005902,,,,
+BMGC_DS05068,BMG_DS011378,21571006,Secondary angle-closure glaucoma,,,,,,,C0271149,,,,,Secondary angle-closure glaucoma | Secondary angle-closure glaucoma (disorder)
+BMGC_DS05069,BMG_DS011381,370504007;10100008,Malignant glaucoma,,,,H40.83,,,C0271152,,,,,Aqueous humor misdirect (disorder) | Aqueous humour misdirect | Aqueous humor misdirect | Ciliary block glaucoma | Malignant glaucoma | Malignant glaucoma | Glaucoma fulminans | Malignant glaucoma (disorder)
+BMGC_DS05070,BMG_DS011383,15374009,Aphakic glaucoma,,,,,,,C0271154,,MTHU002395,,,Aphakic glaucoma | Secondary glaucoma due to aphakia (disorder) | Secondary glaucoma due to aphakia
+BMGC_DS05071,BMG_DS011389,52421005,Incipient cataract,,,,,DOID:10997,immature cataract,C0271163,,,,,Incipient cataract | Water clefts | Incipient cataract (disorder)
+BMGC_DS05072,BMG_DS011391,,,,,,,DOID:13963,nuclear senile cataract,C0271166,,,MONDO:0001847,nuclear senile cataract,
+BMGC_DS05073,BMG_DS011397,,Irvine-Gass Syndrome,Macular Edema,,,,,,C0271178,D008269,,,,
+BMGC_DS05074,BMG_DS011399,34187009,Severe myopia,,,,,,,C0271183,,MTHU002321,,,Severe myopia | High myopia | Severe myopia (disorder)
+BMGC_DS05075,BMG_DS011403,,"Diplopia, Unilateral",Diplopia,,,,,,C0271190,D004172,,,,
+BMGC_DS05076,BMG_DS011412,,"Blindness, Legal",Blindness,,,,,,C0271215,D001766,,,,
+BMGC_DS05077,BMG_DS011428,231906002;26018001;405810005,Oculovestibuloauditory syndrome,,,,,DOID:0060216,Cogan syndrome,C0271270,,,MONDO:0015453,Cogan syndrome,Cogan's syndrome | Oculovestibuloauditory syndrome | Cogan syndrome | Cogan's syndrome (disorder) | Cogan's syndrome | Oculomotor apraxia | Oculomotor apraxia - Cogan type | Oculovestibuloauditory syndrome | Cogan syndrome | Cogan's syndrome (disorder) | Cogan's syndrome (disorder) | Cogan's syndrome | Oculovestibuloauditory syndrome | Cogan syndrome
+BMGC_DS05078,BMG_DS011433,193807000;85430004,Krukenberg spindle,,,,,,,C0271278,,,,,Posterior corneal pigmentation (& [Krukenberg spindle]) | Posterior corneal pigmentation | Krukenberg spindle | Posterior corneal pigmentation (& [Krukenberg spindle]) (disorder) | Krukenberg spindle | Krukenberg spindle (finding)
+BMGC_DS05079,BMG_DS011440,420212002,Schnyder crystalline corneal dystrophy,,,,,DOID:0060456,Schnyder corneal dystrophy,C0271287,C535475,121800,MONDO:0007374,Schnyder corneal dystrophy,Schnyder crystalline corneal dystrophy (disorder) | Schnyder crystalline corneal dystrophy | Schnyder's crystalline corneal dystrophy
+BMGC_DS05080,BMG_DS011459,,,,,,,DOID:9986,orbit lymphoma,C0271333,,,MONDO:0004942,orbit lymphoma,
+BMGC_DS05081,BMG_DS011462,1207009,Glaucomatous atrophy of optic disc,,,,,DOID:10337,glaucomatous atrophy of optic disc,C0271342,,,MONDO:0001006,glaucomatous atrophy of optic disk,Glaucomatous atrophy of optic disc | Glaucomatous atrophy of optic disc (disorder) | Optic disc glaucomatous atrophy | Glaucomatous optic atrophy
+BMGC_DS05082,BMG_DS011471,60750009,Third cranial nerve disorder,,,,,DOID:562,third cranial nerve disease,C0271353,,,MONDO:0003546,third cranial nerve disorder,Third cranial nerve disease | Oculomotor nerve disorder | Third cranial nerve disorder | Oculomotor nerve disease | Third cranial nerve disease (disorder)
+BMGC_DS05083,BMG_DS011472,,Abducens Nerve Diseases,Abducens Nerve Diseases,,,,DOID:10865,abducens nerve palsy,C0271355,D020434,,MONDO:0020594,abducens nerve disorder,
+BMGC_DS05084,BMG_DS011484,,Partial Third-Nerve Palsy,Oculomotor Nerve Diseases,,,,DOID:10864,partial third-nerve palsy,C0271370,D015840,,MONDO:0001144,partial third-nerve palsy,
+BMGC_DS05085,BMG_DS011485,,Total Third-Nerve Palsy,Oculomotor Nerve Diseases,,,,DOID:10866,total third-nerve palsy,C0271371,D015840,,MONDO:0001145,total third-nerve palsy,
+BMGC_DS05086,BMG_DS011486,,Claude Syndrome,Brain Stem Infarctions,,,,,,C0271373,D020526,,,,
+BMGC_DS05087,BMG_DS011488,20610004;67883005,Fourth cranial nerve paresis,,,,,DOID:13864,trochlear nerve disease,C0271375,,,MONDO:0001146,fourth cranial nerve palsy,Fourth nerve palsy | Trochlear nerve palsy | Fourth cranial nerve paralysis | Trochlear nerve paralysis | Fourth cranial nerve paresis | Trochlear nerve weakness | IV nerve palsy | 4th nerve palsy | Superior oblique palsy | Fourth nerve palsy (disorder) | Fourth cranial nerve palsy | Fourth cranial nerve paresis | Fourth cranial nerve paresis (disorder)
+BMGC_DS05088,BMG_DS011491,,Convergence Insufficiency,Ocular Motility Disorders,,,,,,C0271379,D015835,,,,
+BMGC_DS05089,BMG_DS011492,,Convergence Excess,Ocular Motility Disorders,,,,,,C0271380,D015835,,,,
+BMGC_DS05090,BMG_DS011493,,Periodic Alternating Nystagmus,"Nystagmus, Pathologic",,,,,,C0271382,D009759,,,,
+BMGC_DS05091,BMG_DS011494,,Symptomatic Nystagmus,"Nystagmus, Pathologic",,,,,,C0271383,D009759,,,,
+BMGC_DS05092,BMG_DS011495,,Spontaneous Ocular Nystagmus,"Nystagmus, Pathologic",,,,DOID:11771,spontaneous ocular nystagmus,C0271384,D009759,,MONDO:0001361,spontaneous ocular nystagmus,
+BMGC_DS05093,BMG_DS011496,,Horizontal Nystagmus,"Nystagmus, Pathologic",,,,,,C0271385,D009759,,,,
+BMGC_DS05094,BMG_DS011497,,Vertical Nystagmus,"Nystagmus, Pathologic",,,,,,C0271386,D009759,,,,
+BMGC_DS05095,BMG_DS011498,,Rebound Nystagmus,"Nystagmus, Pathologic",,,,,,C0271387,D009759,,,,
+BMGC_DS05096,BMG_DS011499,,Pendular Nystagmus,"Nystagmus, Pathologic",,,,,,C0271388,D009759,,,,
+BMGC_DS05097,BMG_DS011500,,Jerk Nystagmus,"Nystagmus, Pathologic",,,,,,C0271389,D009759,,,,
+BMGC_DS05098,BMG_DS011505,,Paroxysmal Ocular Dyskinesia,Ocular Motility Disorders,,,,,,C0271396,D015835,,,,
+BMGC_DS05099,BMG_DS011521,68996008;155260002,Disorder of middle ear,,,,,DOID:5100,middle ear disease,C0271428,,,MONDO:0003276,middle ear disorder,Disorder of middle ear | Tubotympanic disease | Disorder of middle ear (disorder) | Disorder of middle ear | Disorder of middle ear (disorder)
+BMGC_DS05100,BMG_DS011522,3110003,Acute otitis media,,,,,,,C0271429,,,,,Acute otitis media | Acute otitis media (disorder)
+BMGC_DS05101,BMG_DS011525,35183001,Acute transudative otitis media,,,,,DOID:3697,acute transudative otitis media,C0271432,,,MONDO:0002738,acute transudative otitis media,Acute transudative otitis media | Acute middle ear effusion | Acute MEE - Acute middle ear effusion | Acute transudative otitis media (disorder)
+BMGC_DS05102,BMG_DS011538,275481002,Non-suppurative otitis media,,,,,DOID:11180,non-suppurative otitis media,C0271446,,,MONDO:0001212,non-suppurative otitis media,Non-suppurative otitis media | Non-suppurative otitis media (disorder)
+BMGC_DS05103,BMG_DS011544,38394007,Chronic purulent otitis media,,,,,DOID:14247,chronic purulent otitis media,C0271454,,,MONDO:0001920,chronic purulent otitis media,"Chronic purulent otitis media | Chronic suppurative otitis media | Chronic otitis media with effusion, purulent | CSOM - Chronic suppurative otitis media | Chronic secretory otitis media, purulent | Otitis media with effusion - purulent | Chronic otitis media with perforation | Chronic purulent otitis media (disorder)"
+BMGC_DS05104,BMG_DS011551,,,,,,,DOID:7439,polyp of middle ear,C0271466,,,MONDO:0004223,polyp of middle ear,
+BMGC_DS05105,BMG_DS011611,59572000,Necrosis of pituitary,,,,,DOID:3646,necrosis of pituitary,C0271558,,,MONDO:0002721,necrosis of pituitary,Necrosis of pituitary | Necrosis of pituitary (disorder)
+BMGC_DS05106,BMG_DS011614,44008002,Somatotropin deficiency,,,,,,,C0271561,,,,,Somatotropin deficiency | STH deficiency | GHD | Growth hormone deficiency | Somatotropin deficiency (disorder)
+BMGC_DS05107,BMG_DS011618,,"Isolated Growth Hormone Deficiency, Type II",,,,,DOID:0060872,isolated growth hormone deficiency type II,C0271567,C562704,173100,MONDO:0008250,isolated growth hormone deficiency type II,
+BMGC_DS05108,BMG_DS011619,,Laron Syndrome,Laron Syndrome,,,,DOID:9521,Laron syndrome,C0271568,D046150,262500,MONDO:0009877,Laron syndrome,
+BMGC_DS05109,BMG_DS011624,,"Empty Sella Syndrome, Primary",Empty Sella Syndrome,,,,,,C0271574,D004652,,,,
+BMGC_DS05110,BMG_DS011625,,Pituitary Dwarfism with Large Sella Turcica,,,,,,,C0271575,C562705,262710,MONDO:0009881,pituitary dwarfism with large sella turcica,
+BMGC_DS05111,BMG_DS011627,10340008,Isolated gonadotropin deficiency,,,,,,,C0271577,,,,,Isolated gonadotropin deficiency | Isolated gonadotrophin deficiency | Isolated gonadotropin deficiency (disorder)
+BMGC_DS05112,BMG_DS011628,16041008,Female hypogonadism syndrome,,,,,,,C0271578,,,,,Female hypogonadism syndrome | Female hypogonadism | Female hypogonadism syndrome (disorder)
+BMGC_DS05113,BMG_DS011631,8829008,Isolated lutropin deficiency (disorder),,,,,,,C0271582,,228300,MONDO:0009223,hypogonadotropic hypogonadism 23 with or without anosmia,Isolated lutropin deficiency | Fertile eunuch syndrome | Fertile eunuch | Isolated lutropin deficiency (disorder)
+BMGC_DS05114,BMG_DS011632,,"ACTH Deficiency, Isolated",,,,,,,C0271583,C562707,,,,
+BMGC_DS05115,BMG_DS011634,,,,,,,,,C0271586,,264110,MONDO:0009911,"prolactin deficiency, isolated",
+BMGC_DS05116,BMG_DS011655,19911007,Precocious female puberty,,,,,,,C0271616,,,MONDO:0018561,precocious puberty in female,Precocious female puberty | Precocious female puberty (disorder)
+BMGC_DS05117,BMG_DS011659,33927004,Hypogonadotropic hypogonadism,,5A61.0,Hypopituitarism,E23.0,DOID:0090072;DOID:0090087;DOID:0060875;DOID:0090073;DOID:0090076;DOID:0090092;DOID:0060873;DOID:0090080;DOID:0090075;DOID:0090077;DOID:0090071;DOID:0090082;DOID:0090084;DOID:0090074;DOID:0090093;DOID:0060874;DOID:0090078;DOID:0090070;DOID:0090085;DOID:0090094;DOID:0090086;DOID:0090083;DOID:0090081;DOID:0090079;DOID:0090089;DOID:0090090,hypogonadotropic hypogonadism 5 with or without anosmia | hypogonadotropic hypogonadism 7 with or without anosmia | hypogonadotropic hypogonadism 9 with or without anosmia | isolated growth hormone deficiency type IB | hypogonadotropic hypogonadism 21 with or without anosmia | hypogonadotropic hypogonadism 17 with or without anosmia | hypogonadotropic hypogonadism 6 with or without anosmia | isolated growth hormone deficiency type IA | isolated growth hormone deficiency type III | hypogonadotropic hypogonadism 10 with or without anosmia | hypogonadotropic hypogonadism 2 with or without anosmia | hypogonadotropic hypogonadism 22 with or without anosmia | hypogonadotropic hypogonadism 4 with or without anosmia | hypogonadotropic hypogonadism 1 with or without anosmia | hypogonadotropic hypogonadism 15 with or without anosmia | hypogonadotropic hypogonadism 16 with or without anosmia | hypogonadotropic hypogonadism 3 with or without anosmia | hypogonadotropic hypogonadism 14 with or without anosmia | hypogonadotropic hypogonadism 13 with or without anosmia | hypogonadotropic hypogonadism 19 with or without anosmia | hypogonadotropic hypogonadism 18 with or without anosmia | hypogonadotropic hypogonadism 12 with or without anosmia | hypogonadotropic hypogonadism | hypogonadotropic hypogonadism 11 with or without anosmia | hypogonadotropic hypogonadism 8 with or without anosmia | hypogonadotropic hypogonadism 20 with or without anosmia,C0271623,,MTHU004823,MONDO:0018555,hypogonadotropic hypogonadism,Hypogonadotropic hypogonadism | Secondary hypogonadism | Gonadotrophin deficiency | Hypogonadotropic hypogonadism (disorder)
+BMGC_DS05118,BMG_DS011672,81531005,Type 2 diabetes mellitus in obese,,,,,,,C0271638,,,,,Diabetes mellitus type 2 in obese | Diabetes mellitus type 2 in obese (disorder) | Type 2 diabetes mellitus in obese
+BMGC_DS05119,BMG_DS011680,154720005;9414007,Impaired glucose tolerance (disorder),,,,,DOID:10603,glucose intolerance,C0271650,,,MONDO:0001076,glucose intolerance,Impaired glucose tolerance | Impaired glucose tolerance (disorder) | Impaired glucose tolerance | Prediabetic nonclinical diabetes | Latent diabetes | Chemical diabetes | IGT - Impaired glucose tolerance | Impaired glucose tolerance (disorder)
+BMGC_DS05120,BMG_DS011700,,Symmetric Diabetic Proximal Motor Neuropathy,Diabetic Neuropathies,,,,,,C0271673,D003929,,,,
+BMGC_DS05121,BMG_DS011701,,Asymmetric Diabetic Proximal Motor Neuropathy,Diabetic Neuropathies,,,,,,C0271674,D003929,,,,
+BMGC_DS05122,BMG_DS011703,,"Polyradiculopathy, Abdominal",Polyradiculopathy,,,,,,C0271676,D011128,,,,
+BMGC_DS05123,BMG_DS011704,,Diabetic Mononeuropathy,Diabetic Neuropathies,,,,,,C0271678,D003929,,,,
+BMGC_DS05124,BMG_DS011706,,Diabetic Polyneuropathies,Diabetic Neuropathies,,,,DOID:12785,diabetic polyneuropathy,C0271680,D003929,,MONDO:0001583,diabetic polyneuropathy,
+BMGC_DS05125,BMG_DS011709,,"Polyneuropathy, Motor",Polyneuropathies,,,,,,C0271683,D011115,,MONDO:0002316,motor peripheral neuropathy,
+BMGC_DS05126,BMG_DS011711,,Diabetic Amyotrophy,Diabetic Neuropathies,,,,,,C0271685,D003929,,,,
+BMGC_DS05127,BMG_DS011712,,Diabetic Autonomic Neuropathy,Diabetic Neuropathies,,,,DOID:11503,diabetic autonomic neuropathy,C0271686,D003929,,MONDO:0001299,diabetic autonomic neuropathy,
+BMGC_DS05128,BMG_DS011719,86907008,Acquired generalized lipodystrophy,,,,,,,C0271693,,,MONDO:0019193,acquired generalized lipodystrophy,Acquired generalized lipodystrophy | Acquired lipodystrophic diabetes | Lawrence syndrome | Acquired generalised lipodystrophy | Acquired generalized lipodystrophy (disorder) | Acquired total lipoatrophy
+BMGC_DS05129,BMG_DS011720,49292002,Familial partial lipodystrophy,,,,,DOID:0050440,familial partial lipodystrophy,C0271694,,,MONDO:0020088,familial partial lipodystrophy,Familial lipodystrophy of limbs AND/OR trunk | Familial partial lipodystrophy | Familial partial lipodystrophy (disorder)
+BMGC_DS05130,BMG_DS011721,,Rabson-Mendenhall Syndrome,Donohue Syndrome,,,,DOID:0050470,Donohue syndrome,C0271695,D056731,262190,MONDO:0009874,Rabson-Mendenhall syndrome,
+BMGC_DS05131,BMG_DS011731,,Fasting Hypoglycemia,Hypoglycemia,,,,,,C0271708,D007003,,,,
+BMGC_DS05132,BMG_DS011737,,"Hypoglycemia, leucine-induced",,,,,,,C0271714,C537150,240800;MTHU041972,MONDO:0009415,"hypoglycemia, leucine-induced",
+BMGC_DS05133,BMG_DS011759,45414006,Glucocorticoid deficiency with achalasia,,,,,,,C0271742,,231550,MONDO:0009279,triple-A syndrome,Glucocorticoid deficiency with achalasia | Achalasia-addisonian syndrome | Allgrove syndrome | Triple A syndrome | Alacrimia-achalasia-addisonianism | Glucocorticoid deficiency with achalasia (disorder)
+BMGC_DS05134,BMG_DS011773,,Lingual Goiter,Lingual Goiter,,,,DOID:13196,lingual goiter,C0271760,D047268,,MONDO:0006833,lingual goiter,
+BMGC_DS05135,BMG_DS011793,,,,,,,,,C0271789,,275100,MONDO:0010139,isolated thyroid-stimulating hormone deficiency,
+BMGC_DS05136,BMG_DS011804,26692000,Central hypothyroidism,,,,,,,C0271801,,MTHU047873,,,Central hypothyroidism | Central hypothyroidism (disorder)
+BMGC_DS05137,BMG_DS011827,70348004,Pendred's syndrome,,5A00.00,Permanent congenital hypothyroidism with diffuse goitre,E07.1,DOID:0060744,Pendred Syndrome,C0271829,,274600,MONDO:0010134,Pendred syndrome,Pendred's syndrome | Hypothyroidism with sensorineural deafness | Thyroid hormone organification defect II B | Goiter-deafness syndrome | Genetic defect in thyroid hormonogenesis II B | GDTH IIB | Goitre-deafness syndrome | Pendred's syndrome (disorder) | Pendred syndrome
+BMGC_DS05138,BMG_DS011831,41300001,X-linked reduction of thyroxine-binding globulin,,,,,,,C0271836,,,,,X-linked reduction of thyroxine-binding globulin | X-linked reduction of thyroxine-binding globulin (disorder)
+BMGC_DS05139,BMG_DS011841,54920000;237653008,Familial hyperparathyroidism,,,,,DOID:11202,primary hyperparathyroidism,C0271846,,,MONDO:0016365,familial primary hyperparathyroidism,Familial hyperparathyroidism | Familial hyperparathyroidism (disorder) | Familial hyperparathyroidism | Familial primary hyperparathyroidism | Familial primary hyperparathyroidism (disorder)
+BMGC_DS05140,BMG_DS011842,19034001,Hyperparathyroidism due to renal insufficiency,,,,,DOID:12465,secondary hyperparathyroidism of renal origin,C0271847,,,MONDO:0001530,secondary hyperparathyroidism of renal origin,Hyperparathyroidism due to renal insufficiency | Hyperparathyroidism due to renal insufficiency (disorder) | Secondary hyperparathyroidism of renal origin
+BMGC_DS05141,BMG_DS011847,2243000,Hypercalcemia due to hyperthyroidism,,,,,,,C0271852,,,,,Hypercalcemia due to hyperthyroidism | Hypercalcaemia due to hyperthyroidism | Hypercalcemia due to hyperthyroidism (disorder)
+BMGC_DS05142,BMG_DS011873,,Hypothalamic Pseudopuberty,Hypothalamic Diseases,,,,,,C0271886,D007027,,,,
+BMGC_DS05143,BMG_DS011885,4984008,Microcytic normochromic anemia,,,,,,,C0271902,,,,,Microcytic normochromic anemia | Microcytic normochromic anaemia | Microcytic normochromic anemia (disorder)
+BMGC_DS05144,BMG_DS011892,191245002;267527002,Aplastic anemia due to drugs,,,,,,,C0271909,,,,,Aplastic anemia due to drugs | Hypoplastic anemia due to drug or chemical substance | Hypoplastic anaemia due to drug or chemical substance | Aplastic anaemia due to drugs | Anaemia: [aplastic due to drugs] or [hypoplastic due to drug or chemical substance] | Anemia: [aplastic due to drugs] or [hypoplastic due to drug or chemical substance] | Anaemia: [aplastic due to drugs] or [hypoplastic due to drug or chemical substance] (disorder) | Aplastic anemia due to drugs | Aplastic anaemia due to drugs | Aplastic anemia due to drugs (disorder) | Drug induced aplastic anemia | Drug induced aplastic anaemia
+BMGC_DS05145,BMG_DS011914,49708008,Anemia of chronic renal failure,,,,,,,C0271932,,,,,Anemia of chronic renal failure | Anaemia of chronic renal failure | Anemia of chronic renal failure (disorder) | Anemia of chronic renal insufficiency | Anaemia of chronic renal insufficiency
+BMGC_DS05146,BMG_DS011915,59548005,"Congenital dyserythropoietic anemia, type I",,,,,DOID:0111397,congenital dyserythropoietic anemia type Ib,C0271933,,,MONDO:0020337,congenital dyserythropoietic anemia type 1,"Congenital dyserythropoietic anemia, type I | Congenital dyserythropoietic anaemia, type I | Congenital dyserythropoietic anemia, type I (disorder) | Congenital dyserythropoietic anaemia type I | Congenital dyserythropoietic anemia type I"
+BMGC_DS05147,BMG_DS011916,26409005,"Congenital dyserythropoietic anemia, type III",,,,,DOID:0111399,congenital dyserythropoietic anemia type IIIa,C0271934,,,,,"Congenital dyserythropoietic anemia, type III | Congenital dyserythropoietic anaemia, type III | Congenital dyserythropoietic anemia, type III (disorder) | Congenital dyserythropoietic anaemia type III | Congenital dyserythropoietic anemia type III"
+BMGC_DS05148,BMG_DS011950,12907000,Thiamine-responsive megaloblastic anemia,,,,,,,C0271972,,,,,Thiamine-responsive megaloblastic anemia | Thiamine-responsive megaloblastic anaemia | Thiamine-responsive megaloblastic anemia (disorder)
+BMGC_DS05149,BMG_DS011955,,Thalassemia Intermedia,beta-Thalassemia,,,,,,C0271979,D017086,,,,
+BMGC_DS05150,BMG_DS011956,86715000,Beta zero thalassemia,,,,,,,C0271980,,,,,Beta 0 thalassemia | Beta 0 thalassaemia | Beta zero thalassemia | Beta zero thalassaemia | Beta zero thalassemia (disorder) | beta zero thalassemia | beta zero thalassaemia
+BMGC_DS05151,BMG_DS011961,,Delta-Beta Thalassemia,,,,,,,C0271985,C562716,,MONDO:0016489,delta-beta-thalassemia,
+BMGC_DS05152,BMG_DS011966,,delta-Thalassemia,delta-Thalassemia,,,,,,C0271990,D055538,,,,
+BMGC_DS05153,BMG_DS011967,62074008,Delta zero thalassemia,,,,,,,C0271991,,,,,Delta zero thalassemia (disorder) | Delta zero thalassaemia | Delta 0 thalassaemia | Delta 0 thalassemia | Delta zero thalassemia
+BMGC_DS05154,BMG_DS011970,16964007,Hereditary persistence of fetal hemoglobin thalassemia,,,,,,,C0271994,,,MONDO:0018749,hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome,Hereditary persistence of fetal hemoglobin thalassemia | Hereditary persistence of fetal haemoglobin thalassaemia | Hereditary persistence of fetal hemoglobin thalassemia (disorder) | Hereditary persistence of foetal haemoglobin thalassaemia | HPFH (hereditary persistence of fetal haemoglobin) beta-thalassaemia syndrome | HPFH (hereditary persistence of fetal hemoglobin) beta-thalassemia syndrome
+BMGC_DS05155,BMG_DS011981,5300004,Hemoglobin Bart's hydrops syndrome,,,,,,,C0272005,,,MONDO:0015579,Hb Bart's hydrops fetalis,Hemoglobin Bart's hydrops syndrome | Hemoglobin Bart's disease | Alpha thalassemia major | Hemoglobin Barts hydrops | Haemoglobin Bart's hydrops syndrome | Alpha thalassaemia major | Haemoglobin Bart's disease | Haemoglobin Barts hydrops | Hemoglobin Bart's hydrops syndrome (disorder) | Haemoglobin Bart hydrops syndrome | Hemoglobin Bart hydrops syndrome
+BMGC_DS05156,BMG_DS012021,87994004,Xerocytosis,,,,,DOID:0111575,dehydrated hereditary stomatocytosis,C0272051,,,MONDO:0017910,dehydrated hereditary stomatocytosis,Xerocytosis | Dessicocytosis | Xerocytosis (disorder)
+BMGC_DS05157,BMG_DS012022,,Rh Deficiency Syndrome,,,,,DOID:0050641,Rh deficiency syndrome,C0272052,C562717,268150,MONDO:0019107,Rh deficiency syndrome,
+BMGC_DS05158,BMG_DS012023,111577008,Anemia due to enzyme deficiency,,,,,,,C0272053,,,,,Anemia due to enzyme deficiency | Anaemia due to enzyme deficiency | Anemia due to enzyme deficiency (disorder)
+BMGC_DS05159,BMG_DS012025,22933009,G-6-PD class I variant anemia,,,,,,,C0272056,,,,,G-6-PD class I variant anemia | G-6-PD class I variant anaemia | Glucose-6-phosphate dehydrogenase deficiency class I variant anemia | Glucose-6-phosphate dehydrogenase deficiency class I variant anemia (disorder) | Glucose-6-phosphate dehydrogenase deficiency class I variant anaemia
+BMGC_DS05160,BMG_DS012033,52413004,HNSHA due to glucose phosphate isomerase deficiency,,,,,,,C0272064,,,,,HNSHA due to glucose phosphate isomerase deficiency | Hereditary nonspherocytic hemolytic anemia (HNSHA) due to glucose phosphate isomerase deficiency | Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to glucose phosphate isomerase deficiency | Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency (disorder) | Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency | Hereditary nonspherocytic haemolytic anaemia due to glucose phosphate isomerase deficiency
+BMGC_DS05161,BMG_DS012035,,Glycogen Storage Disease XII,,,,,,,C0272066,C562718,611881,MONDO:0012747,glycogen storage disease due to aldolase A deficiency,
+BMGC_DS05162,BMG_DS012038,62268000,HNSHA due to diphosphoglycerate mutase deficiency,,,,,,,C0272069,,,,,HNSHA due to diphosphoglycerate mutase deficiency | Hereditary nonspherocytic hemolytic anemia (HNSHA) due to diphosphoglycerate mutase deficiency | Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to diphosphoglycerate mutase deficiency | Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency | Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency (disorder) | Hereditary nonspherocytic haemolytic anaemia due to diphosphoglycerate mutase deficiency
+BMGC_DS05163,BMG_DS012048,66729008,Hemoglobin D disease,,,,,DOID:5378,hemoglobin D disease,C0272080,,,MONDO:0019537,hemoglobin D disease,Hemoglobin D disease | Hemoglobin D-D disease | Haemoglobin D disease | Haemoglobin D-D disease | Hemoglobin D disease (disorder)
+BMGC_DS05164,BMG_DS012052,,,,,,,,,C0272084,,,MONDO:0016670,sickle cell-hemoglobin d disease syndrome,
+BMGC_DS05165,BMG_DS012054,,Congenital Methemoglobinemia,,,,,,,C0272087,C580280,,MONDO:0018963,hereditary methemoglobinemia,
+BMGC_DS05166,BMG_DS012092,75331009,Evans syndrome,,,,D69.41,DOID:8931,Evans' syndrome,C0272126,,,MONDO:0016030,Evans syndrome,Evans syndrome | Evans syndrome (disorder)
+BMGC_DS05167,BMG_DS012103,,Tn Syndrome,,,,,,,C0272137,C562719,300622,MONDO:0010381,Tn polyagglutination syndrome,
+BMGC_DS05168,BMG_DS012110,19588001,Erythrocytosis due to tissue hypoxemia,,,,,,,C0272144,,,,,Erythrocytosis due to tissue hypoxemia | Erythrocytosis due to tissue hypoxaemia | Erythrocytosis due to tissue hypoxemia (disorder)
+BMGC_DS05169,BMG_DS012118,32984002,Neonatal polycythemia,,,,,DOID:11242,plethora of newborn,C0272153,,,MONDO:0001238,polycythemia neonatorum,Neonatal polycythemia | Polycythemia neonatorum | Plethora of newborn | Neonatal polycythaemia | Polycythaemia neonatorum | Neonatal polycythemia (disorder)
+BMGC_DS05170,BMG_DS012129,111584000,Reticular dysgenesis,,,,,DOID:0060020,reticular dysgenesis,C0272167,C538361,267500,MONDO:0009973,reticular dysgenesis,"Reticular dysgenesis | De Vaal disease | Immunoerythromyeloid hypoplasia | Severe combined immunodeficiency, neutropaenia and thrombocytopaenia | SCID - Severe combined immunodeficiency, neutropaenia and thrombocytopaenia | Congenital aleukia | Reticular dysgenesia | Generalised haematopoietic hypoplasia | Generalized hematopoietic hypoplasia | Reticular dysgenesis (disorder) | SCID - Severe combined immunodeficiency, neutropenia and thrombocytopenia | Severe combined immunodeficiency, neutropenia and thrombocytopenia"
+BMGC_DS05171,BMG_DS012132,89454001,Shwachman syndrome,,,,,,,C0272170,,,MONDO:0009833,Shwachman-Diamond syndrome,"Shwachman syndrome | Shwachman-Diamond syndrome | Metaphyseal chondrodysplasia with pancreatic insufficiency AND neutropenia | Metaphyseal dysplasia with malabsorption and neutropenia | Metaphyseal chondrodysplasia, Shwachman type | Schwachman's syndrome | Schwachman-Diamond syndrome | Schwachman-Bodian syndrome | Shwachman's syndrome | Congenital lipomatosis of pancreas | Schwachmann-Diamond syndrome | Shwachman syndrome (disorder)"
+BMGC_DS05172,BMG_DS012136,,Lazy Leukocyte Syndrome,,,,,,,C0272174,C562721,150550,MONDO:0007883,"periodic fever, immunodeficiency, and thrombocytopenia syndrome",
+BMGC_DS05173,BMG_DS012138,14333004,Alloimmune neonatal neutropenia,,,,,,,C0272176,,,MONDO:0018739,neonatal alloimmune neutropenia,Alloimmune neonatal neutropenia | Isoimmune neonatal neutropenia | Neonatal isoimmune neutropenia | Alloimmune neonatal neutropenia (disorder)
+BMGC_DS05174,BMG_DS012140,47318007,Drug-induced neutropenia,,,,,,,C0272178,,,,,Drug-induced neutropenia | Idiosyncratic neutropenia | Drug-induced neutropenia (disorder) | Drug-associated agranulocytosis | Drug induced neutropenia
+BMGC_DS05175,BMG_DS012147,77358003,Congenital leukocyte adherence deficiency,,,,,,,C0272187,,,MONDO:0017570,leukocyte adhesion deficiency,Congenital leukocyte adherence deficiency | Leukocyte adhesion deficiency | Congenital leucocyte adherence deficiency | Leucocyte adhesion deficiency | Congenital leukocyte adherence deficiency (disorder)
+BMGC_DS05176,BMG_DS012151,79336007,Familial eosinophilia,,,,D72.19,,,C0272192,C562722,131400,MONDO:0007544,"eosinophilia, familial",Familial eosinophilia | Familial eosinophilia (disorder)
+BMGC_DS05177,BMG_DS012158,,Familial Hemophagocytic Lymphocytosis,"Lymphohistiocytosis, Hemophagocytic",,,,,,C0272199,D051359,,MONDO:0015541,hereditary hemophagocytic lymphohistiocytosis,
+BMGC_DS05178,BMG_DS012160,,,,,,,DOID:4659,extracutaneous mastocytoma,C0272202,,,MONDO:0019025,extracutaneous mastocytoma,
+BMGC_DS05179,BMG_DS012161,,,,,,,DOID:4660,indolent systemic mastocytosis,C0272203,,,MONDO:0020331,indolent systemic mastocytosis,
+BMGC_DS05180,BMG_DS012184,36980009,SCID (severe combined immunodeficiency) due to absent adenosine deaminase,,,,,,,C0272230,,,,,Severe combined immunodeficiency due to absent adenosine deaminase | Severe combined immunodeficiency due to absent adenosine deaminase (disorder) | SCID (severe combined immunodeficiency) due to absent ADA (adenosine deaminase) | SCID (severe combined immunodeficiency) due to absent adenosine deaminase
+BMGC_DS05181,BMG_DS012189,82286005,Hyperimmunoglobulin M syndrome,,,,,DOID:0080544,hyper IgM syndrome,C0272236,,,MONDO:0003947,hyper-IgM syndrome,Hyperimmunoglobulin M syndrome | Hyperimmunoglobulin M syndrome (disorder) | Immunodeficiency with IgM hypergammaglobulinaemia | Immunodeficiency with IgM hypergammaglobulinemia | Hyper IgM syndrome
+BMGC_DS05182,BMG_DS012190,88714009,Transient hypogammaglobulinemia of infancy,,4A01.03,Transient hypogammaglobulinaemia of infancy,D80.7,DOID:624,transient hypogammaglobulinemia of infancy,C0272238,,,MONDO:0015698,transient hypogammaglobulinemia of infancy,Transient hypogammaglobulinemia of infancy | Immunoglobulin maturational delay | THI - Transient hypogammaglobulinemia of infancy | Transient hypogammaglobulinaemia of infancy | THI - Transient hypogammaglobulinaemia of infancy | Transient hypogammaglobulinemia of infancy (disorder)
+BMGC_DS05183,BMG_DS012193,,Complement Deficiencies,Hereditary Complement Deficiency Diseases,,,,DOID:626,complement deficiency,C0272242,D000081208,,MONDO:0003832,complement deficiency,
+BMGC_DS05184,BMG_DS012204,,,,,,,DOID:3722,solitary osseous plasmacytoma,C0272256,,,MONDO:0002755,solitary osseous plasmacytoma,
+BMGC_DS05185,BMG_DS012231,73397007,Heparin-induced thrombocytopenia,,,,,,,C0272285,,,MONDO:0018048,heparin-induced thrombocytopenia,Heparin-induced thrombocytopenia | Heparin-induced thrombocytopenia (disorder) | Heparin induced thrombocytopaenia | Heparin induced thrombocytopenia
+BMGC_DS05186,BMG_DS012232,2897005,Thrombocytopenia due to platelet alloimmunization,,,,,DOID:1587,thrombocytopenia due to platelet alloimmunization,C0272286,,,MONDO:0002048,thrombocytopenia due to immune destruction,Thrombocytopenia due to immune destruction | Immune thrombocytopenia | Immune thrombocytopenia (disorder) | ITP - immune thrombocytopenia
+BMGC_DS05187,BMG_DS012237,13172003,Chronic idiopathic thrombocytopenic purpura,,,,,,,C0272293,,,,,Chronic idiopathic thrombocytopenic purpura | Werlhof's disease | Purpura hemorrhagica | Chronic thrombocytopenic purpura | Autoimmune thrombocytopenic purpura | Purpura haemorrhagica | Chronic idiopathic thrombocytopenic purpura (disorder)
+BMGC_DS05188,BMG_DS012245,,Gray Platelet Syndrome,Gray Platelet Syndrome,,,,DOID:0111049;DOID:0111044,gray platelet syndrome | platelet-type bleeding disorder 17,C0272302,D055652,139090,MONDO:0007686,gray platelet syndrome,
+BMGC_DS05189,BMG_DS012256,86075001,Coagulation factor deficiency syndrome,,,,,,,C0272315,,,,,Coagulation factor deficiency syndrome | Coagulation factor disorder | Blood clotting factor deficiency disorder | Coagulation factor deficiency syndrome (disorder)
+BMGC_DS05190,BMG_DS012258,33297000,Hereditary factor II deficiency disease,,,,,DOID:2235,prothrombin deficiency,C0272317,,613679,MONDO:0013361,congenital prothrombin deficiency,Hereditary factor II deficiency disease | Hereditary hypoprothrombinemia | Hereditary hypoprothrombinaemia | Hereditary factor II deficiency disease (disorder)
+BMGC_DS05191,BMG_DS012261,40855001,Hereditary factor VII deficiency disease,,,,,,,C0272320,,227500,MONDO:0009211,congenital factor VII deficiency,Hereditary factor VII deficiency syndrome | Hereditary hypoproconvertinemia | Hereditary hypoproconvertinaemia | Hereditary factor VII deficiency disease (disorder) | Hereditary factor VII deficiency disease
+BMGC_DS05192,BMG_DS012263,16872008,Severe hereditary factor VIII deficiency disease,,,,,,,C0272322,,,MONDO:0015719,severe hemophilia A,Severe hemophilia A | Severe haemophilia A | Severe hereditary factor VIII deficiency disease (disorder) | Severe hereditary factor VIII deficiency disease
+BMGC_DS05193,BMG_DS012264,33344008,Moderate hereditary factor VIII deficiency disease,,,,,,,C0272323,,,MONDO:0015720,moderately severe hemophilia A,Moderate hemophilia A | Moderate haemophilia A | Moderate hereditary factor VIII deficiency disease (disorder) | Moderate hereditary factor VIII deficiency disease
+BMGC_DS05194,BMG_DS012265,26029002,Mild hereditary factor VIII deficiency disease,,,,,,,C0272324,,,MONDO:0015721,mild hemophilia A,Mild hemophilia A | Mild haemophilia A | Mild hereditary factor VIII deficiency disease (disorder) | Mild hereditary factor VIII deficiency disease
+BMGC_DS05195,BMG_DS012266,,"Factor 8 deficiency, acquired",,,,,,,C0272325,C536392,,MONDO:0035735,acquired hemophilia A,
+BMGC_DS05196,BMG_DS012267,37350004,Hereditary factor X deficiency disease,,,,,,,C0272327,,227600,MONDO:0009212,congenital factor X deficiency,Hereditary factor X deficiency disease | Hereditary Stuart factor deficiency disease | Hereditary Stuart-Prower deficiency disease | Hereditary factor X deficiency disease (disorder)
+BMGC_DS05197,BMG_DS012276,48976006,Prekallikrein deficiency,,,,,,,C0272339,,MTHU050385,MONDO:0044744,prekallikrein deficiency,Prekallikrein deficiency | Fletcher factor deficiency | Prekallikrein deficiency (disorder) | Fletcher trait
+BMGC_DS05198,BMG_DS012277,27312002,High molecular weight kininogen deficiency,,,,,DOID:0111676,high molecular weight kininogen deficiency,C0272340,C537060,228960,MONDO:0009234,congenital high-molecular-weight kininogen deficiency,High molecular weight kininogen deficiency | Fitzgerald factor deficiency | High molecular weight kininogen deficiency (disorder) | Fitzgerald-Flaujeac-Williams-Reid trait
+BMGC_DS05199,BMG_DS012286,,"Dysfibrinogenemia, Congenital",,,,,,,C0272350,C562727,616004,MONDO:0014452,familial dysfibrinogenemia,
+BMGC_DS05200,BMG_DS012294,60078000;234451005,Acquired von Willebrand disease,,,,D68.04,DOID:0111146,acquired von Willebrand syndrome,C0272362,,,MONDO:0020460,acquired von willebrand syndrome,Acquired von Willebrand disease | Acquired von Willebrand syndrome | Acquired von Willebrand syndrome (disorder) | Acquired von Willebrand's disease | Acquired von Willebrand syndrome | Acquired von Willebrand disease | Acquired von Willebrand disease (disorder)
+BMGC_DS05201,BMG_DS012303,16773005,Drug-induced coagulation inhibitor disorder,,,,,,,C0272373,,,,,Drug-induced coagulation inhibitor disorder | Drug-induced coagulation inhibitor disorder (disorder)
+BMGC_DS05202,BMG_DS012305,,Antithrombin III Deficiency,Antithrombin III Deficiency,,,,DOID:3755,antithrombin III deficiency,C0272375,D020152,613118,MONDO:0013144,hereditary antithrombin deficiency,
+BMGC_DS05203,BMG_DS012318,76616003,Disorder of lymph node,,,,,DOID:9942,lymph node disease,C0272394,,,MONDO:0004928,lymph node disorder,Disorder of lymph node | Disorder of lymph node (disorder)
+BMGC_DS05204,BMG_DS012329,43325004,Nontraumatic splenic rupture,,,,,,,C0272409,,,,,Nontraumatic splenic rupture | Nontraumatic splenic rupture (disorder) | Non-traumatic rupture of spleen | Spontaneous rupture of spleen
+BMGC_DS05205,BMG_DS012332,82053000,Splenic abscess,,,,,DOID:2530,splenic abscess,C0272412,,,MONDO:0002333,splenic abscess,Splenic abscess | Splenic abscess (disorder) | Abscess of spleen | Spleen abscess
+BMGC_DS05206,BMG_DS012428,63171007,Acute infectious disease,,,,,,,C0275518,,,,,Acute infectious disease | Acute infection | Acute infectious disease (disorder)
+BMGC_DS05207,BMG_DS012449,31860008,Acute bacterial peritonitis,,,,,,,C0275550,,,,,Acute bacterial peritonitis | Acute bacterial peritonitis (disorder)
+BMGC_DS05208,BMG_DS012454,21060003,Acute bacterial epiglottitis,,,,,,,C0275555,,,,,Acute bacterial epiglottitis | Acute bacterial epiglottitis (disorder)
+BMGC_DS05209,BMG_DS012455,75498004,Acute bacterial sinusitis,,,,,,,C0275556,,,,,Acute bacterial sinusitis | Acute bacterial sinusitis (disorder)
+BMGC_DS05210,BMG_DS012458,21846001,Pulmonary actinomycosis,,1C10.0,Pulmonary actinomycosis,A42.0,,,C0275566,,,,,Pulmonary actinomycosis | Thoracic actinomycosis | Pulmonary actinomycosis (disorder)
+BMGC_DS05211,BMG_DS012468,,Nocardia asteroides Infection,Nocardia Infections,,,,,,C0275578,D009617,,,,
+BMGC_DS05212,BMG_DS012471,,Pulmonary Nocardiosis,Nocardia Infections,,,,,,C0275583,D009617,,,,
+BMGC_DS05213,BMG_DS012522,29864006,Acute gonococcal urethritis,,,,,,,C0275652,,,,,Acute gonococcal urethritis | Acute inflammation of urethra caused by Neisseria gonorrhoeae (disorder) | Acute inflammation of urethra caused by Neisseria gonorrhoeae
+BMGC_DS05214,BMG_DS012524,45377007,Acute gonococcal salpingitis,,,,,DOID:13942,acute gonococcal salpingitis,C0275654,,,MONDO:0001837,acute gonococcal salpingitis,Acute gonococcal salpingitis | Acute gonococcal salpingitis (disorder)
+BMGC_DS05215,BMG_DS012532,42746002,Gonorrhea of rectum,,,,,,,C0275665,,,,,Gonorrhea of rectum | Gonorrhoea of rectum | Rectal gonorrhoea | Rectal gonorrhea | Infection of rectum caused by Neisseria gonorrhoeae (disorder) | Infection of rectum caused by Neisseria gonorrhoeae
+BMGC_DS05216,BMG_DS012598,77116006,Infection due to Bordetella parapertussis (disorder),,,,,DOID:11750,Bordetella parapertussis whooping cough,C0275742,,,MONDO:0001353,Bordetella parapertussis infectious disease,Bordetella parapertussis infection | Infection caused by Bordetella parapertussis | Infection caused by Bordetella parapertussis (disorder)
+BMGC_DS05217,BMG_DS012611,76651006,Pneumococcal pharyngitis,,,,,,,C0275761,,,,,Pneumococcal pharyngitis | Pneumococcal pharyngitis (disorder)
+BMGC_DS05218,BMG_DS012627,77863005,Lyme carditis,,,,,,,C0275778,,,,,Lyme carditis | Lyme carditis (disorder)
+BMGC_DS05219,BMG_DS012637,11461005,Staphylococcal tonsillitis,,,,,,,C0275793,,,,,Staphylococcal tonsillitis | Staphylococcal tonsillitis (disorder)
+BMGC_DS05220,BMG_DS012638,82228008,Staphylococcal pharyngitis,,,,,,,C0275794,,,,,Staphylococcal pharyngitis | Staphylococcal pharyngitis (disorder)
+BMGC_DS05221,BMG_DS012647,41582007,Streptococcal tonsillitis,,CA03.0,Streptococcal tonsillitis,J03.0,,,C0275804,,,,,Streptococcal tonsillitis | Streptococcal tonsillitis (disorder)
+BMGC_DS05222,BMG_DS012682,31137003,"Early latent syphilis, positive serology, negative cerebrospinal fluid, less than 2 years after infection",,,,,,,C0275842,,,MONDO:0040922,latent early syphilis,"Early latent syphilis, positive serology, negative cerebrospinal fluid, less than 2 years after infection (disorder) | Early latent syphilis, positive serology, negative cerebrospinal fluid, less than 2 years after infection"
+BMGC_DS05223,BMG_DS012784,25629007,Acute tuberculosis,,,,,,,C0275959,,,,,Acute tuberculosis | Acute tuberculosis (disorder)
+BMGC_DS05224,BMG_DS012800,111835002,Infection by Campylobacter fetus,,,,,,,C0275979,,,MONDO:0040728,Campylobacter fetus infectious disease,Infection by Campylobacter fetus | Infection by Vibrio fetus | Infection caused by Campylobacter fetus | Infection caused by Vibrio fetus | Infection caused by Campylobacter fetus (disorder)
+BMGC_DS05225,BMG_DS012803,18081009,Enteric campylobacteriosis,,,,,,,C0275982,,,,,Enteric campylobacteriosis | Enteric campylobacteriosis (disorder) | Campylobacter diarrhoea | Campylobacter diarrhea | Campylobacter intestinal infection
+BMGC_DS05226,BMG_DS012809,49442000,Initial lesion of yaws,,,,,DOID:10568,early yaws,C0275990,,,,,Initial lesion of yaws | Primary stage of yaws | Mother yaw | Chancre of yaws | Primary framboesia | Primary frambesia | Initial framboesia | Initial yaws lesion | Yaws chancre | Initial lesion of yaws (disorder) | Initial frambesia
+BMGC_DS05227,BMG_DS012813,23191004,Early yaws,,,,,DOID:10568,early yaws,C0275998,,,MONDO:0001067,early yaws,Early yaws | Early yaws (disorder)
+BMGC_DS05228,BMG_DS012819,186968004,Yaws gummata and ulcers,,,,,DOID:10567,late yaws,C0276007,,,,,Yaws gummata and ulcers | Yaws gummata and ulcers (disorder)
+BMGC_DS05229,BMG_DS012836,70036007,Haemophilus influenzae pneumonia,,,,,,,C0276026,,,,,Haemophilus influenzae pneumonia | Haemophilus influenzae pneumonia (disorder)
+BMGC_DS05230,BMG_DS012837,19021002,Haemophilus influenzae otitis media,,,,,,,C0276027,,,,,Haemophilus influenzae otitis media | Haemophilus influenzae otitis media (disorder)
+BMGC_DS05231,BMG_DS012867,1201760007,Sepsis caused by Bacteroides,,,,,,,C0276064,,,,,Sepsis caused by Bacteroides (disorder) | Sepsis caused by Bacteroides | Septicemia caused by Bacteroides | Septicaemia caused by Bacteroides
+BMGC_DS05232,BMG_DS012873,11218009,Infection caused by Pseudomonas aeruginosa,,,,,,,C0276075,,,MONDO:0040732,Pseudomonas aeruginosa infectious disease,Infection caused by Pseudomonas aeruginosa | Infection caused by Pseudomonas aeruginosa (disorder)
+BMGC_DS05233,BMG_DS012875,16664009,Malignant otitis media,,,,,,,C0276077,,,,,Malignant otitis media | Otitis media due to Pseudomonas aeruginosa | Malignant otitis media (disorder)
+BMGC_DS05234,BMG_DS012881,17732003,Ecthyma gangrenosum,,,,,,,C0276085,,MTHU076646,,,Ecthyma gangrenosum | Ecthyma gangrenosum (disorder)
+BMGC_DS05235,BMG_DS012883,9323009,Escherichia coli septicemia,,,,,,,C0276088,,,,,Septicemia due to E. Coli | Septicemic colibacillosis | E. coli septicemia | Escherichia coli septicemia | E. coli septicaemia | Escherichia coli septicaemia | Septicaemic colibacillosis | Septicaemia due to E. Coli | Septicemia due to Escherichia coli (disorder) | Septicemia due to Escherichia coli | Septicaemia due to Escherichia coli
+BMGC_DS05236,BMG_DS012884,51530003,Pneumonia caused by Escherichia coli,,,,,,,C0276089,,,,,Escherichia coli pneumonia | Pneumonia caused by E. coli | Pneumonia caused by Escherichia coli (disorder) | Pneumonia caused by Escherichia coli
+BMGC_DS05237,BMG_DS012923,89141000,Viral myocarditis,,,,B33.22,,,C0276138,,,MONDO:0023161,viral myocarditis,Viral myocarditis | Viral myocarditis (disorder)
+BMGC_DS05238,BMG_DS012960,186582008;240466002;25157001;359814004,Monkeypox (disorder),,,,,DOID:3292,mpox,C0276180,,,MONDO:0002594,monkeypox,Monkeypox | Monkeypox (disorder) | Monkeypox | Monkeypox (disorder) | Monkey pox | Mpox
+BMGC_DS05239,BMG_DS012997,37323009,Recurrent herpes simplex,,,,,,,C0276223,,,,,Recurrent herpes simplex | Recurrent herpes simplex (disorder)
+BMGC_DS05240,BMG_DS013000,79450003;428638009,Herpes encephalitis,,,,,,,C0276226,,MTHU061461,MONDO:0012521,herpes simplex encephalitis,Herpes encephalitis | HSE - Herpes simplex encephalitis | Herpes simplex encephalitis | Herpetic encephalitis | Herpetic meningoencephalitis | Herpes encephalitis (disorder) | Herpes encephalitis | Encephalitis caused by Herpesvirus | Encephalitis caused by Herpesvirus (disorder) | Encephalitis caused by Herpesviridae
+BMGC_DS05241,BMG_DS013002,72321008,Herpes simplex keratoconjunctivitis,,,,,,,C0276228,,,,,Herpes simplex keratoconjunctivitis | Herpes simplex keratoconjunctivitis (disorder) | HSV keratoconjunctivitis
+BMGC_DS05242,BMG_DS013030,123156006;81652008;240539000;1296946004,Verruca plana,,,,B07.8,,,C0276262,,,,,Verruca plana | Verruca plana (disorder) | Verruca plana | Flat wart | Verruca plana (disorder) | Plane wart | Plane wart (disorder) | Verruca plana | Flat wart | Verruca plana (morphologic abnormality) | Verruca plana
+BMGC_DS05243,BMG_DS013052,,Zika Virus Infection,Zika Virus Infection,,,,DOID:0060478,Zika fever,C0276289,D000071243,,MONDO:0018661,Zika virus infectious disease,
+BMGC_DS05244,BMG_DS013106,24662006,"Influenza due to Influenza virus, type B",,,,,,,C0276353,,,,,Influenza caused by Influenza B virus (disorder) | Influenza caused by Influenza B virus
+BMGC_DS05245,BMG_DS013213,,,,,,,,,C0276496,,,MONDO:0100087,familial Alzheimer disease,
+BMGC_DS05246,BMG_DS013215,40780007,Human immunodeficiency virus I infection,,,,,,,C0276500,,,,,Human immunodeficiency virus I infection | Human immunodeficiency virus I infection (disorder) | Human immunodeficiency virus 1 infection
+BMGC_DS05247,BMG_DS013266,420691000,Nutritional deficiency with AIDS (acquired immunodeficiency syndrome),,,,,,,C0276587,,,,,Nutritional deficiency with acquired immunodeficiency syndrome (disorder) | Nutritional deficiency with AIDS (acquired immunodeficiency syndrome) | Nutritional deficiency with acquired immunodeficiency syndrome
+BMGC_DS05248,BMG_DS013285,186639003,Chronic viral hepatitis B without delta-agent,,1E51.0Z,"Chronic hepatitis B, unspecified",B18.1,,,C0276610,,,,,Chronic viral hepatitis B without delta-agent | Chronic viral hepatitis B without delta-agent (disorder)
+BMGC_DS05249,BMG_DS013317,86348002,Mycotic endocarditis,,,,,,,C0276648,,,MONDO:0042433,mycotic endocarditis,Mycotic endocarditis | Fungal endocarditis | Mycotic endocarditis (disorder)
+BMGC_DS05250,BMG_DS013322,,Invasive Pulmonary Aspergillosis,Invasive Pulmonary Aspergillosis,,,,,,C0276653,D055744,,,,
+BMGC_DS05251,BMG_DS013333,187031007;85055004,Disseminated coccidioidomycosis,,1F25.10,Disseminated coccidioidomycosis,B38.7,,,C0276667,,,,,Disseminated coccidioidomycosis | Extra-pulmonary coccidioidomycosis | Disseminated coccidioidomycosis (disorder)
+BMGC_DS05252,BMG_DS013345,3973009;414821002,Neonatal candidiasis,,KA63.2,Neonatal candidosis,P37.5,DOID:9577,neonatal candidiasis,C0276682,,,MONDO:0004824,neonatal candidiasis,Neonatal monilia infection | Neonatal moniliasis | Neonatal candida infection | Neonatal candidosis | Neonatal monilia | Neonatal candidiasis | Neonatal monilia infection (disorder) | Neonatal candidiasis (disorder) | Neonatal candidiasis | Neonatal candida infection | Neonatal candidosis | Neonatal thrush
+BMGC_DS05253,BMG_DS013349,20953001,Pulmonary cryptococcosis,,1F27.0,Pulmonary cryptococcosis,B45.0,,,C0276688,,,,,Pulmonary cryptococcosis | Pulmonary cryptococcosis (disorder)
+BMGC_DS05254,BMG_DS013384,91051003,Disseminated sporotrichosis,,1F2J.3,Disseminated sporotrichosis,B42.7,,,C0276725,,,MONDO:0042484,disseminated sporotrichosis,Disseminated sporotrichosis | Disseminated sporotrichosis (disorder)
+BMGC_DS05255,BMG_DS013386,87603003,Lymphocutaneous sporotrichosis,,1F2J.0,Lymphocutaneous sporotrichosis,B42.1,,,C0276727,,,,,Lymphocutaneous sporotrichosis | Lymphocutaneous sporotrichosis (disorder)
+BMGC_DS05256,BMG_DS013401,19087001,Kerion celsi,,,,,,,C0276742,,275240,MONDO:0010146,Kerion celsi,Tinea kerion | Kerion | Kerion celsi | Tinea kerion (disorder) | Suppurative dermatophytosis | Suppurative ringworm
+BMGC_DS05257,BMG_DS013413,56922006,Onychomycosis caused by Trichophyton rubrum,,,,,,,C0276754,,,,,Onychomycosis caused by Trichophyton rubrum (disorder) | Onychomycosis caused by Trichophyton rubrum
+BMGC_DS05258,BMG_DS013414,23549005,Onychomycosis caused by Trichophyton mentagrophytes,,,,,,,C0276755,,,,,Onychomycosis caused by Trichophyton mentagrophytes | Onychomycosis caused by Trichophyton mentagrophytes (disorder)
+BMGC_DS05259,BMG_DS013417,,Fusariosis,Fusariosis,,,,DOID:0050289,fusariosis,C0276758,D060585,,MONDO:0016426,fusariosis,
+BMGC_DS05260,BMG_DS013471,52281009,Meningoencephalitis caused by Naegleria,,,,,,,C0276824,,,,,Meningoencephalitis caused by Naegleria (disorder) | Meningoencephalitis caused by Naegleria
+BMGC_DS05261,BMG_DS013556,60979006,Schistosoma hematobium infection,,,,,DOID:1394,urinary schistosomiasis,C0276926,,,,,Vesical schistosomiasis | Bladder schistosomiasis | Schistosomiasis of bladder | Schistosoma haematobium infection | Schistosoma haematobium infection (disorder)
+BMGC_DS05262,BMG_DS013562,52179003,Infection by Schistosoma intercalatum,,,,,DOID:0050597,intestinal schistosomiasis,C0276932,,,MONDO:0044351,Schistosoma intercalatum infectious disease,Infection by Schistosoma intercalatum | Infection caused by Schistosoma intercalatum | Infection caused by Schistosoma intercalatum (disorder)
+BMGC_DS05263,BMG_DS013625,,Opisthorchis felineus Infection,Opisthorchiasis,,,,,,C0277004,D009889,,,,
+BMGC_DS05264,BMG_DS013626,,Opisthorchis viverrini Infection,Opisthorchiasis,,,,,,C0277005,D009889,,,,
+BMGC_DS05265,BMG_DS013736,35033008,Angiostrongylus cantonensis infection,,,,,DOID:0050256,angiostrongyliasis,C0277131,C536369,,,,Infection by Angiostrongylus cantonensis | Angiostrongylus cantonensis infection | Infection caused by Angiostrongylus cantonensis | Infection caused by Angiostrongylus cantonensis (disorder)
+BMGC_DS05266,BMG_DS013753,91156005,Infection by Baylisascaris,,,,,,,C0277150,,,MONDO:0000297,baylisascariasis,Infection by Baylisascaris | Infection caused by Baylisascaris | Infection caused by Baylisascaris (disorder)
+BMGC_DS05267,BMG_DS013922,2341000,Infection by Moniliformis,,,,,,,C0277334,,,,,Infection by Moniliformis | Moniliformiosis | Infection caused by Moniliformis (disorder) | Infection caused by Moniliformis
+BMGC_DS05268,BMG_DS013942,,Flea Infestation,Flea Infestations,,,,,,C0277355,D058267,,,,
+BMGC_DS05269,BMG_DS014094,39341005,Infectious colitis,,,,,,,C0277524,,,MONDO:0006039,infectious colitis,Infectious colitis | Septic colitis | Infectious colitis (disorder) | Infective colitis
+BMGC_DS05270,BMG_DS014095,186157003;12463005,Infectious gastroenteritis,,,,,,,C0277525,,,,,Infectious gastroenteritis | Infectious gastroenteritis (disorder) | Infectious gastroenteritis | Septic gastroenteritis | Gastric flu | Infectious gastroenteritis (disorder)
+BMGC_DS05271,BMG_DS014098,11840006,Traveler's diarrhea,,,,,,,C0277528,,,,,Traveler's diarrhea | Turista | Traveler's diarrhoea | Traveler's diarrhea (disorder)
+BMGC_DS05272,BMG_DS014143,,"Hemiplegia, Crossed",Hemiplegia,,,,,,C0278110,D006429,,MONDO:0016210,alternating hemiplegia,
+BMGC_DS05273,BMG_DS014153,,,,,,,,,C0278151,,134300,MONDO:0007593,facial spasm,
+BMGC_DS05274,BMG_DS014164,,"Reflex Epilepsy, Reading","Epilepsy, Reflex",,,,,,C0278193,D020195,132300,MONDO:0007560,reading seizures,
+BMGC_DS05275,BMG_DS014168,,"Reflex Epilepsy, Musicogenic","Epilepsy, Reflex",,,,,,C0278198,D020195,,,,
+BMGC_DS05276,BMG_DS014176,,,,,,,DOID:3869,childhood medulloblastoma,C0278510,,,MONDO:0002797,childhood medulloblastoma,
+BMGC_DS05277,BMG_DS014177,,,,,,,DOID:3356,localized osteosarcoma,C0278511,,,MONDO:0002620,localized osteosarcoma,
+BMGC_DS05278,BMG_DS014178,,,,,,,DOID:6286,childhood cerebellar astrocytic neoplasm,C0278594,,,MONDO:0003842,childhood cerebellar astrocytic neoplasm,
+BMGC_DS05279,BMG_DS014179,,,,,,,DOID:3516,adult fibrosarcoma,C0278595,,,MONDO:0002676,adult fibrosarcoma,
+BMGC_DS05280,BMG_DS014180,,,,,,,DOID:7501,childhood infratentorial ependymoma,C0278599,,,MONDO:0004248,pediatric infratentorial ependymoma,
+BMGC_DS05281,BMG_DS014181,,,,,,,DOID:6383,childhood brain stem glioma,C0278600,,,MONDO:0003869,childhood brain stem glioma,
+BMGC_DS05282,BMG_DS014182,,,,,,,DOID:6263,inflammatory breast carcinoma,C0278601,,,MONDO:0006804,inflammatory breast carcinoma,
+BMGC_DS05283,BMG_DS014183,,,,,,,DOID:5693,adult liposarcoma,C0278608,,,MONDO:0003585,adult liposarcoma,
+BMGC_DS05284,BMG_DS014184,,,,,,,DOID:3720,extramedullary plasmacytoma,C0278619,,,MONDO:0002754,extramedullary plasmacytoma,
+BMGC_DS05285,BMG_DS014185,,,,,,,DOID:9544,refractory plasma cell neoplasm,C0278620,,,MONDO:0004816,refractory plasma cell neoplasm,
+BMGC_DS05286,BMG_DS014186,,,,,,,DOID:8369,adult malignant schwannoma,C0278622,,,MONDO:0004545,adult malignant schwannoma,
+BMGC_DS05287,BMG_DS014187,,,,,,,DOID:7502,childhood supratentorial ependymoma,C0278650,,,MONDO:0004249,pediatric supratentorial ependymoma,
+BMGC_DS05288,BMG_DS014188,,,,,,,DOID:6576,childhood optic nerve glioma,C0278653,,,MONDO:0003932,childhood optic nerve glioma,
+BMGC_DS05289,BMG_DS014189,,,,,,,DOID:3717,gastric adenocarcinoma,C0278701,,,MONDO:0005036,gastric adenocarcinoma,
+BMGC_DS05290,BMG_DS014191,,,,,,,DOID:4653,intraocular retinoblastoma,C0278717,,,MONDO:0003077,intraocular retinoblastoma,
+BMGC_DS05291,BMG_DS014192,,,,,,,DOID:4656,extraocular retinoblastoma,C0278719,,,MONDO:0003078,extraocular retinoblastoma,
+BMGC_DS05292,BMG_DS014193,,,,,,,DOID:1790,malignant mesothelioma,C0278752,,,,,
+BMGC_DS05293,BMG_DS014194,,,,,,,DOID:6052,central nervous system childhood germ cell tumor,C0278754,,,MONDO:0003750,childhood central nervous system germ cell tumor,
+BMGC_DS05294,BMG_DS014195,,,,,,,DOID:3590,gestational trophoblastic neoplasm,C0278796,,,,,
+BMGC_DS05295,BMG_DS014196,,,,,,,DOID:4906,small intestine adenocarcinoma,C0278803,,,MONDO:0003198,small intestine adenocarcinoma,
+BMGC_DS05296,BMG_DS014197,,,,,,,DOID:10816,duodenum adenocarcinoma,C0278804,,,MONDO:0006186,duodenal adenocarcinoma,
+BMGC_DS05297,BMG_DS014198,,,,,,,DOID:13996,small intestine lymphoma,C0278805,,,MONDO:0001852,small intestine lymphoma,
+BMGC_DS05298,BMG_DS014199,,,,,,,DOID:3121,gallbladder cancer,C0278806,,,,,
+BMGC_DS05299,BMG_DS014200,,,,,,,DOID:3283,invasive malignant thymoma,C0278846,,,MONDO:0002592,invasive malignant thymoma,
+BMGC_DS05300,BMG_DS014201,,,,,,,DOID:7214,noninvasive malignant thymoma,C0278847,,,MONDO:0004147,noninvasive malignant thymoma,
+BMGC_DS05301,BMG_DS014204,,,,,,,DOID:5716,hormone producing pituitary cancer,C0278864,,,MONDO:0006238,growth hormone-producing pituitary gland adenoma,
+BMGC_DS05302,BMG_DS014205,,,,,,,DOID:6566,posterior uveal melanoma,C0278867,,,MONDO:0024863,small size posterior uveal melanoma,
+BMGC_DS05303,BMG_DS014206,,,,,,,DOID:6566,posterior uveal melanoma,C0278868,,,MONDO:0024864,medium/large size posterior uveal melanoma,
+BMGC_DS05304,BMG_DS014208,,,,,,,DOID:4813,adult brain stem glioma,C0278873,,,MONDO:0003153,adult brainstem glioma,
+BMGC_DS05305,BMG_DS014209,,,,,,,DOID:3864,adult medulloblastoma,C0278876,,,MONDO:0002794,adult medulloblastoma,
+BMGC_DS05306,BMG_DS014210,,,,,,,DOID:3068,glioblastoma,C0278878,,,MONDO:0020690,adult glioblastoma,
+BMGC_DS05307,BMG_DS014211,,,,,,,,,C0278883,,,MONDO:0005191,metastatic melanoma,
+BMGC_DS05308,BMG_DS014212,,,,,,,DOID:7827,adult extraosseous osteosarcoma,C0278985,,,MONDO:0004374,adult extraskeletal osteosarcoma,
+BMGC_DS05309,BMG_DS014213,,,,,,,,,C0278996,,,MONDO:0005627,head and neck cancer,
+BMGC_DS05310,BMG_DS014214,,,,,,,DOID:686,liver carcinoma,C0279000,,,MONDO:0018531,carcinoma of liver and intrahepatic biliary tract,
+BMGC_DS05311,BMG_DS014215,,,,,,,DOID:6053,childhood germ cell cancer,C0279014,,,MONDO:0003751,childhood germ cell tumor,
+BMGC_DS05312,BMG_DS014216,,,,,,,DOID:0081308,grade I lymphomatoid granulomatosis,C0279065,,,MONDO:0859747,grade I lymphomatoid granulomatosis,
+BMGC_DS05313,BMG_DS014218,,,,,,,DOID:3186,adult oligodendroglioma,C0279070,,,MONDO:0002543,adult oligodendroglioma,
+BMGC_DS05314,BMG_DS014220,,,,,,,DOID:6898,ovarian seromucinous carcinoma,C0279392,,,MONDO:0004032,ovarian seromucinous carcinoma,
+BMGC_DS05315,BMG_DS014222,,,,,,,,,C0279543,,608232,MONDO:0011996,"chronic myelogenous leukemia, BCR-ABL1 positive",
+BMGC_DS05316,BMG_DS014223,,,,,,,DOID:4239,alveolar soft part sarcoma,C0279544,,,,,
+BMGC_DS05317,BMG_DS014224,,,,,,,DOID:8282,adult epithelioid sarcoma,C0279545,,,MONDO:0004521,adult epithelioid sarcoma,
+BMGC_DS05318,BMG_DS014225,,,,,,,DOID:6332,adult malignant hemangiopericytoma,C0279547,,,MONDO:0003856,adult malignant hemangiopericytoma,
+BMGC_DS05319,BMG_DS014226,,,,,,,DOID:5894,adult malignant mesenchymoma,C0279548,,,MONDO:0003692,adult malignant mesenchymoma,
+BMGC_DS05320,BMG_DS014227,,,,,,,DOID:4829,adenosquamous lung carcinoma,C0279557,,,MONDO:0004973,adenosquamous lung carcinoma,
+BMGC_DS05321,BMG_DS014229,,,,,,,,,C0279565,,,MONDO:0005051,invasive lobular breast carcinoma,
+BMGC_DS05322,BMG_DS014232,,,,,,,DOID:5602,T-cell adult acute lymphocytic leukemia,C0279592,,,MONDO:0003539,T-cell adult acute lymphocytic leukemia,
+BMGC_DS05323,BMG_DS014234,,,,,,,DOID:7603,fibrosarcomatous osteosarcoma,C0279602,,,MONDO:0004301,fibrosarcomatous osteosarcoma,
+BMGC_DS05324,BMG_DS014235,,,,,,,DOID:3372,chondroblastic osteosarcoma,C0279603,,,MONDO:0002627,chondroblastic osteosarcoma,
+BMGC_DS05325,BMG_DS014236,,,,,,,,,C0279606,,,MONDO:0018055,pediatric hepatocellular carcinoma,
+BMGC_DS05326,BMG_DS014237,,,,,,,DOID:0070328,adult hepatocellular carcinoma,C0279607,,,MONDO:0016216,adult hepatocellular carcinoma,
+BMGC_DS05327,BMG_DS014238,,,,,,,DOID:5189,epithelial predominant Wilms' tumor,C0279608,,,MONDO:0003322,epithelial predominant Wilms' tumor,
+BMGC_DS05328,BMG_DS014239,,,,,,,DOID:5182,blastema predominant kidney Wilms' tumor,C0279609,,,MONDO:0003320,blastema predominant kidney Wilms tumor,
+BMGC_DS05329,BMG_DS014240,,,,,,,DOID:5191,stromal predominant kidney Wilms' tumor,C0279610,,,MONDO:0006432,stromal predominant kidney Wilms tumor,
+BMGC_DS05330,BMG_DS014241,,,,,,,DOID:5179,mixed cell type kidney Wilms' tumor,C0279611,,,MONDO:0003318,mixed cell type kidney Wilms' tumor,
+BMGC_DS05331,BMG_DS014242,,,,,,,DOID:4051,alveolar rhabdomyosarcoma,C0279613,,,,,
+BMGC_DS05332,BMG_DS014243,,,,,,,DOID:7463,childhood pleomorphic rhabdomyosarcoma,C0279614,,,MONDO:0004233,childhood pleomorphic rhabdomyosarcoma,
+BMGC_DS05333,BMG_DS014244,,,,,,,DOID:3377,small cell osteogenic sarcoma,C0279622,,,MONDO:0002630,small cell osteogenic sarcoma,
+BMGC_DS05334,BMG_DS014245,,,,,,,DOID:3748,esophagus squamous cell carcinoma,C0279626,,,MONDO:0005580,esophageal squamous cell carcinoma,
+BMGC_DS05335,BMG_DS014246,,,,,,,DOID:4914,esophagus adenocarcinoma,C0279628,,,MONDO:0005028,esophageal adenocarcinoma,
+BMGC_DS05336,BMG_DS014248,,,,,,,DOID:6217,gastric diffuse adenocarcinoma,C0279635,,,MONDO:0005017,diffuse gastric adenocarcinoma,
+BMGC_DS05337,BMG_DS014249,,,,,,,DOID:4908,anal carcinoma,C0279637,,,MONDO:0003199,anal carcinoma,
+BMGC_DS05338,BMG_DS014250,,,,,,,DOID:3029,colon mucinous adenocarcinoma,C0279639,,,MONDO:0005007,colon mucinous adenocarcinoma,
+BMGC_DS05339,BMG_DS014252,,,,,,,DOID:3500,gallbladder adenocarcinoma,C0279651,,,MONDO:0006215,gallbladder adenocarcinoma,
+BMGC_DS05340,BMG_DS014253,,,,,,,DOID:3709,rectum mucinous adenocarcinoma,C0279652,,,MONDO:0002748,rectum mucinous adenocarcinoma,
+BMGC_DS05341,BMG_DS014255,,,,,,,DOID:7707,rectum signet ring adenocarcinoma,C0279654,,,MONDO:0004336,rectal signet ring cell adenocarcinoma,
+BMGC_DS05342,BMG_DS014256,,,,,,,DOID:5535,gallbladder squamous cell carcinoma,C0279658,,,MONDO:0006220,gallbladder squamous cell carcinoma,
+BMGC_DS05343,BMG_DS014257,,,,,,,DOID:3495,extrahepatic bile duct adenocarcinoma,C0279659,,,MONDO:0002665,extrahepatic bile duct adenocarcinoma,
+BMGC_DS05344,BMG_DS014258,,,,,,,DOID:5742,pancreatic acinar cell adenocarcinoma,C0279661,,,MONDO:0006346,pancreatic acinar cell carcinoma,
+BMGC_DS05345,BMG_DS014259,,,,,,,DOID:5746,ovarian serous cystadenocarcinoma,C0279663,,,MONDO:0006046,ovarian serous cystadenocarcinoma,
+BMGC_DS05346,BMG_DS014260,,,,,,,DOID:3604,ovarian mucinous cystadenocarcinoma,C0279665,,,MONDO:0002701,ovarian mucinous cystadenocarcinoma,
+BMGC_DS05347,BMG_DS014261,,,,,,,DOID:7438,ovarian clear cell cystadenocarcinoma,C0279667,,,MONDO:0004222,ovarian clear cell cystadenocarcinoma,
+BMGC_DS05348,BMG_DS014263,,,,,,,DOID:3744,cervical squamous cell carcinoma,C0279671,,,MONDO:0006143,cervical squamous cell carcinoma,
+BMGC_DS05349,BMG_DS014264,,,,,,,DOID:3702,cervical adenocarcinoma,C0279672,,,MONDO:0005153,cervical adenocarcinoma,
+BMGC_DS05350,BMG_DS014265,,,,,,,DOID:6740,cervix small cell carcinoma,C0279674,,,MONDO:0006142,cervical small cell carcinoma,
+BMGC_DS05351,BMG_DS014266,,,,,,,DOID:4006,bladder urothelial carcinoma,C0279680,,,MONDO:0005611,bladder transitional cell carcinoma,
+BMGC_DS05352,BMG_DS014267,,,,,,,DOID:3742,bladder squamous cell carcinoma,C0279681,,,MONDO:0002760,bladder squamous cell carcinoma,
+BMGC_DS05353,BMG_DS014268,,,,,,,DOID:3711,bladder adenocarcinoma,C0279682,,,MONDO:0002751,bladder adenocarcinoma,
+BMGC_DS05354,BMG_DS014270,,,,,,,DOID:6992,intraocular mixed cell type melanoma,C0279693,,,MONDO:0004062,intermediate cell type uveal melanoma,
+BMGC_DS05355,BMG_DS014271,,,,,,,DOID:7808,necrotic uveal melanoma,C0279695,,,MONDO:0004365,necrotic uveal melanoma,
+BMGC_DS05356,BMG_DS014272,,,,,,,,,C0279697,,,MONDO:0044740,salivary gland squamous cell carcinoma,
+BMGC_DS05357,BMG_DS014274,,,,,,,DOID:7609,parathyroid transitional clear cell adenoma,C0279700,,,MONDO:0004303,parathyroid gland clear cell adenoma,
+BMGC_DS05358,BMG_DS014275,,,,,,,DOID:7610,mixed cell type adenoma of parathyroid,C0279701,,,MONDO:0004304,mixed cell type adenoma of parathyroid,
+BMGC_DS05359,BMG_DS014276,,,,,,,DOID:4467,clear cell renal cell carcinoma,C0279702,,,MONDO:0005005,clear cell renal carcinoma,
+BMGC_DS05360,BMG_DS014277,,,,,,,DOID:7926,epithelial malignant thymoma,C0279705,,,MONDO:0006458,thymoma type B3,
+BMGC_DS05361,BMG_DS014278,,,,,,,DOID:7599,lymphoepithelioma-like thymic carcinoma,C0279706,,,MONDO:0004297,lymphoepithelioma-like thymic carcinoma,
+BMGC_DS05362,BMG_DS014279,,,,,,,DOID:7927,malignant type A thymoma,C0279707,,,MONDO:0004400,malignant type A thymoma,
+BMGC_DS05363,BMG_DS014280,,,,,,,DOID:5344,testicular yolk sac tumor,C0279708,,,MONDO:0003402,testicular yolk sac tumor,
+BMGC_DS05364,BMG_DS014284,,,,,,,DOID:2870,endometrial adenocarcinoma,C0279763,,,,,
+BMGC_DS05365,BMG_DS014285,,,,,,,DOID:5299,endometrial clear cell adenocarcinoma,C0279765,,,MONDO:0006191,endometrial clear cell adenocarcinoma,
+BMGC_DS05366,BMG_DS014286,,,,,,,DOID:711,refractory hairy cell leukemia,C0279780,,,,,
+BMGC_DS05367,BMG_DS014287,,,,,,,DOID:8272,anterior urethra cancer,C0279930,,,MONDO:0004518,anterior urethra cancer,
+BMGC_DS05368,BMG_DS014288,,,,,,,DOID:7488,posterior urethra cancer,C0279931,,,MONDO:0004240,posterior urethra cancer,
+BMGC_DS05369,BMG_DS014289,,,,,,,DOID:4985,extraosseous Ewings sarcoma-primitive neuroepithelial tumor,C0279980,,,MONDO:0018270,extraskeletal Ewing sarcoma,
+BMGC_DS05370,BMG_DS014290,,,,,,,DOID:3520,childhood fibrosarcoma,C0279981,,,MONDO:0002678,pediatric fibrosarcoma,
+BMGC_DS05371,BMG_DS014291,,,,,,,DOID:7731,childhood malignant hemangiopericytoma,C0279983,,,MONDO:0004344,childhood malignant hemangiopericytoma,
+BMGC_DS05372,BMG_DS014292,,,,,,,DOID:5695,childhood liposarcoma,C0279984,,,MONDO:0003587,pediatric liposarcoma,
+BMGC_DS05373,BMG_DS014293,,,,,,,DOID:4239,alveolar soft part sarcoma,C0279985,,,,,
+BMGC_DS05374,BMG_DS014294,,,,,,,DOID:7732,childhood malignant schwannoma,C0279987,,,MONDO:0004345,childhood malignant schwannoma,
+BMGC_DS05375,BMG_DS014295,,,,,,,DOID:4505,childhood angiosarcoma,C0279988,,,MONDO:0003022,pediatric angiosarcoma,
+BMGC_DS05376,BMG_DS014296,,,,,,,DOID:7095,childhood epithelioid sarcoma,C0279989,,,MONDO:0004105,childhood epithelioid sarcoma,
+BMGC_DS05377,BMG_DS014297,,,,,,,DOID:5893,childhood malignant mesenchymoma,C0279991,,,MONDO:0003691,childhood malignant mesenchymoma,
+BMGC_DS05378,BMG_DS014299,,,,,,,,,C0280089,,,MONDO:0006041,lung carcinoid tumor,
+BMGC_DS05379,BMG_DS014300,,,,,,,DOID:5567,ovarian germ cell teratoma,C0280131,,,MONDO:0005602,ovarian teratoma,
+BMGC_DS05380,BMG_DS014301,,,,,,,DOID:2641,ovarian germ cell monodermal and highly specialized teratoma,C0280134,,,MONDO:0002372,ovarian monodermal and highly specialized teratoma,
+BMGC_DS05381,BMG_DS014302,,,,,,,DOID:5936,ovarian mixed germ cell neoplasm,C0280135,,,MONDO:0003710,ovarian mixed germ cell neoplasm,
+BMGC_DS05382,BMG_DS014303,,,,,,,,,C0280141,,,MONDO:0020321,acute undifferentiated leukemia,
+BMGC_DS05383,BMG_DS014307,,,,,,,,,C0280302,,,MONDO:0021427,squamous cell carcinoma of lip,
+BMGC_DS05384,BMG_DS014311,,,,,,,,,C0280313,,,MONDO:0044704,oropharynx squamous cell carcinoma,
+BMGC_DS05385,BMG_DS014313,,,,,,,,,C0280321,,,MONDO:0044638,hypopharynx squamous cell carcinoma,
+BMGC_DS05386,BMG_DS014314,,,,,,,DOID:2876,laryngeal squamous cell carcinoma,C0280324,,,MONDO:0005595,laryngeal squamous cell carcinoma,
+BMGC_DS05387,BMG_DS014315,,,,,,,DOID:7031,glottis squamous cell carcinoma,C0280325,,,MONDO:0004080,glottis squamous cell carcinoma,
+BMGC_DS05388,BMG_DS014316,,,,,,,DOID:7585,subglottis squamous cell carcinoma,C0280326,,,MONDO:0004291,subglottis squamous cell carcinoma,
+BMGC_DS05389,BMG_DS014317,,,,,,,DOID:3752,larynx verrucous carcinoma,C0280328,,,MONDO:0002766,larynx verrucous carcinoma,
+BMGC_DS05390,BMG_DS014318,,,,,,,DOID:7583,glottis verrucous carcinoma,C0280329,,,MONDO:0004289,glottis verrucous carcinoma,
+BMGC_DS05391,BMG_DS014319,,,,,,,DOID:7584,subglottis verrucous carcinoma,C0280330,,,MONDO:0004290,subglottis verrucous carcinoma,
+BMGC_DS05392,BMG_DS014320,,,,,,,DOID:7586,supraglottis verrucous carcinoma,C0280331,,,MONDO:0004292,supraglottis verrucous carcinoma,
+BMGC_DS05393,BMG_DS014321,,,,,,,,,C0280332,,,MONDO:0044787,nasal cavity and paranasal sinus squamous cell carcinoma,
+BMGC_DS05394,BMG_DS014322,,,,,,,DOID:5515,nasal cavity squamous cell carcinoma,C0280333,,,MONDO:0006059,nasal cavity squamous cell carcinoma,
+BMGC_DS05395,BMG_DS014323,,,,,,,DOID:0050619,paranasal sinus cancer,C0280334,,,MONDO:0044705,paranasal sinus squamous cell carcinoma,
+BMGC_DS05396,BMG_DS014324,,,,,,,DOID:4633,nasal cavity inverting papilloma,C0280336,,,MONDO:0003065,nasal cavity inverting papilloma,
+BMGC_DS05397,BMG_DS014325,,,,,,,DOID:7174,anus basaloid carcinoma,C0280470,,,MONDO:0004130,anus basaloid carcinoma,
+BMGC_DS05398,BMG_DS014326,,,,,,,DOID:3183,childhood oligodendroglioma,C0280475,,,MONDO:0002540,childhood oligodendroglioma,
+BMGC_DS05399,BMG_DS014327,,,,,,,DOID:3545,childhood choroid plexus cancer,C0280623,,,MONDO:0024744,childhood choroid plexus neoplasm,
+BMGC_DS05400,BMG_DS014328,,,,,,,DOID:6171,uterine carcinosarcoma,C0280630,,,MONDO:0006485,uterine carcinosarcoma,
+BMGC_DS05401,BMG_DS014329,,,,,,,DOID:5289,uterus leiomyosarcoma,C0280631,,,MONDO:0016262,leiomyosarcoma of the corpus uteri,
+BMGC_DS05402,BMG_DS014331,,,,,,,DOID:4593,childhood meningioma,C0280656,,,MONDO:0003057,pediatric meningioma,
+BMGC_DS05403,BMG_DS014332,,,,,,,DOID:4947,cholangiocarcinoma,C0280725,,,,,
+BMGC_DS05404,BMG_DS014333,,,,,,,DOID:2146,ovary sarcoma,C0280746,,,MONDO:0002225,ovarian sarcoma,
+BMGC_DS05405,BMG_DS014334,,,,,,,DOID:6811,juvenile pilocytic astrocytoma,C0280783,,,MONDO:0003999,juvenile pilocytic astrocytoma,
+BMGC_DS05406,BMG_DS014336,,,,,,,DOID:5890,malignant adult ependymoma,C0280787,,,MONDO:0003690,adult anaplastic ependymoma,
+BMGC_DS05407,BMG_DS014337,,,,,,,,,C0280788,,,MONDO:0016700,anaplastic ependymoma,
+BMGC_DS05408,BMG_DS014338,,,,,,,DOID:7907,mixed astrocytoma-ependymoma,C0280791,,,MONDO:0004393,mixed astrocytoma-ependymoma,
+BMGC_DS05409,BMG_DS014339,,,,,,,DOID:7817,mixed astrocytoma-ependymoma-oligodendroglioma,C0280792,,,MONDO:0004366,mixed astrocytoma-ependymoma-oligodendroglioma,
+BMGC_DS05410,BMG_DS014340,,,,,,,DOID:7912,mixed oligodendroglioma-astrocytoma,C0280793,,,,,
+BMGC_DS05411,BMG_DS014341,,,,,,,DOID:5031,adult pineal parenchymal tumor,C0280794,,,MONDO:0003248,adult pineal parenchymal tumor,
+BMGC_DS05412,BMG_DS014342,,,,,,,DOID:4858,pineal gland astrocytoma,C0280795,,,MONDO:0003171,pineal gland astrocytoma,
+BMGC_DS05413,BMG_DS014343,,,,,,,DOID:5349,central nervous system adult germ cell tumor,C0280796,,,MONDO:0003405,adult central nervous system germ cell tumor,
+BMGC_DS05414,BMG_DS014345,,,,,,,DOID:3234,central nervous system lymphoma,C0280803,,,MONDO:0002571,primary central nervous system lymphoma,
+BMGC_DS05415,BMG_DS014346,,,,,,,DOID:2101,vulva squamous cell carcinoma,C0280856,,,MONDO:0024609,vulvar squamous cell carcinoma,
+BMGC_DS05416,BMG_DS014349,,,,,,,DOID:6741,bilateral breast cancer,C0281267,,,MONDO:0003982,bilateral breast carcinoma,
+BMGC_DS05417,BMG_DS014350,,,,,,,DOID:7656,adult infiltrating astrocytic neoplasm,C0281329,,,MONDO:0004320,adult infiltrating astrocytic neoplasm,
+BMGC_DS05418,BMG_DS014351,,,,,,,DOID:7631,"adult embryonal tumor with multilayered rosettes, C19MC-altered",C0281330,,,MONDO:0004310,"adult embryonal tumor with multilayered rosettes, c19mc-altered",
+BMGC_DS05419,BMG_DS014352,,,,,,,DOID:6648,adult pineoblastoma,C0281332,,,MONDO:0003957,adult pineoblastoma,
+BMGC_DS05420,BMG_DS014353,,,,,,,DOID:7826,adult papillary meningioma,C0281334,,,MONDO:0004373,adult papillary meningioma,
+BMGC_DS05421,BMG_DS014354,,,,,,,DOID:4074,pancreatic adenocarcinoma,C0281361,,,MONDO:0006047,pancreatic adenocarcinoma,
+BMGC_DS05422,BMG_DS014356,,,,,,,,,C0281508,,,MONDO:0019373,desmoplastic small round cell tumor,
+BMGC_DS05423,BMG_DS014357,,,,,,,DOID:775,intraocular lymphoma,C0281658,,,MONDO:0004351,intraocular lymphoma,
+BMGC_DS05424,BMG_DS014377,22932004;398958000,"Chondrodysplasia punctata, X-linked dominant type",,,,,,,C0282102,,302960,MONDO:0020603,X-linked chondrodysplasia punctata 2,"Chondrodysplasia punctata, Conradi-Hünermann type | Conradi-Hünermann syndrome | Conradi's syndrome | Chondrodysplasia punctata, Conradi-Hunermann type | Conradi-Hunermann syndrome | Chondrodysplasia punctata, X-linked dominant type | Chondrodysplasia calcificans congenita | Chondrodysplasia punctata, Conradi-Hünermann type (disorder) | Chondrodysplasia punctata, X-linked dominant type (disorder) | Chondrodysplasia punctata, X-linked dominant type | Conradi Hünermann Happle syndrome | X-linked chondrodysplasia punctata type 2 | Chondrodystrophia calcificans congenita | Happle syndrome"
+BMGC_DS05425,BMG_DS014378,,,,,,,DOID:4964,neurotic disorder,C0282126,,,MONDO:0024614,neurotic depression,
+BMGC_DS05426,BMG_DS014379,,,,,,,,,C0282160,,107600,MONDO:0007145,aplasia cutis congenita,
+BMGC_DS05427,BMG_DS014381,,Iron Overload,Iron Overload,,,,,,C0282193,D019190,,,,
+BMGC_DS05428,BMG_DS014383,,Cronkhite-Canada Syndrome,Cronkhite-Canada Syndrome,,,,,,C0282207,D000098858,175500,MONDO:0008283,Cronkhite-Canada syndrome,
+BMGC_DS05429,BMG_DS014384,,Amaurotic Familial Idiocy,Tay-Sachs Disease,,,,,,C0282220,D013661,,,,
+BMGC_DS05430,BMG_DS014387,,Bubonic Plague,Plague,,,,DOID:10773,bubonic plague,C0282312,D010930,,MONDO:0001112,bubonic plague,
+BMGC_DS05431,BMG_DS014388,,Interstitial Cystitis,"Cystitis, Interstitial",,,,DOID:13949,interstitial cystitis,C0282488,D018856,,MONDO:0018301,interstitial cystitis,
+BMGC_DS05432,BMG_DS014389,,Sneddon Syndrome,Sneddon Syndrome,,,,DOID:13096,Sneddon syndrome,C0282492,D018860,182410,MONDO:0008436,Sneddon syndrome,
+BMGC_DS05433,BMG_DS014390,,Environmental Illness,Environmental Illness,,,,,,C0282504,D018876,,,,
+BMGC_DS05434,BMG_DS014391,,Landau-Kleffner Syndrome,Landau-Kleffner Syndrome,,,,DOID:2538,Landau-Kleffner syndrome,C0282512,D018887,245570,MONDO:0009509,Landau-Kleffner syndrome,
+BMGC_DS05435,BMG_DS014392,,,,,,,,,C0282513,,,MONDO:0019806,primary progressive aphasia,
+BMGC_DS05436,BMG_DS014393,,"Adrenoleukodystrophy, Neonatal",Peroxisomal Disorders,,,,,,C0282525,D018901,,,,
+BMGC_DS05437,BMG_DS014394,,Hyperpipecolic Acidemia,Peroxisomal Disorders,,,,,,C0282526,D018901,,,,
+BMGC_DS05438,BMG_DS014395,,"Refsum Disease, Infantile","Refsum Disease, Infantile",,,,DOID:0050444,infantile Refsum disease,C0282527,D052919,601539,MONDO:0011101;MONDO:0019174,obsolete infantile Refsum disease | peroxisome biogenesis disorder 1B,
+BMGC_DS05439,BMG_DS014396,,Peroxisomal Disorders,Peroxisomal Disorders,,,,DOID:906,peroxisomal disease,C0282528,D018901,,MONDO:0019053,peroxisomal disease,
+BMGC_DS05440,BMG_DS014397,,"Chondrodysplasia Punctata, Rhizomelic","Chondrodysplasia Punctata, Rhizomelic",,,,DOID:2580,rhizomelic chondrodysplasia punctata,C0282529,D018902,,MONDO:0015776,rhizomelic chondrodysplasia punctata,
+BMGC_DS05441,BMG_DS014398,30419000,Leukostasis,Leukostasis,,,,DOID:12986,leukostasis,C0282548,D018921,,MONDO:0006831,leukostasis,Leukostasis | Leukostasis (morphologic abnormality)
+BMGC_DS05442,BMG_DS014399,,Persian Gulf Syndrome,Persian Gulf Syndrome,,,,DOID:4491,persian gulf syndrome,C0282550,D018923,,MONDO:0005907,persian gulf syndrome,
+BMGC_DS05443,BMG_DS014400,,Congenital Disorders of Glycosylation,Congenital Disorders of Glycosylation,,,,DOID:5212,congenital disorder of glycosylation,C0282577,D018981,,MONDO:0015286,congenital disorder of glycosylation,
+BMGC_DS05444,BMG_DS014401,,,,,,,DOID:461,muscle benign neoplasm,C0282606,,,MONDO:0021545,myomatous neoplasm,
+BMGC_DS05445,BMG_DS014402,,,,,,,DOID:175,vascular cancer,C0282607,,,MONDO:0024296,vascular neoplasm,
+BMGC_DS05446,BMG_DS014403,,,,,,,,,C0282609,,,MONDO:0005374,bone marrow neoplasm,
+BMGC_DS05447,BMG_DS014406,,"Smith-Lemli-Opitz Syndrome, Type I",Smith-Lemli-Opitz Syndrome,,,,,,C0282643,D019082,,,,
+BMGC_DS05448,BMG_DS014407,,"Smith-Lemli-Opitz Syndrome, Type II",Smith-Lemli-Opitz Syndrome,,,,,,C0282644,D019082,,,,
+BMGC_DS05449,BMG_DS014410,,"Hemorrhagic Fever, Ebola","Hemorrhagic Fever, Ebola",,,,DOID:4325,Ebola hemorrhagic fever,C0282687,D019142,,MONDO:0005737,Ebola hemorrhagic fever,
+BMGC_DS05450,BMG_DS014411,187098003;59277005,Phycomycosis,Zygomycosis,,,,,,C0300933,D020096,,,,Zygomycosis (& [mucormycosis]) | Zygomycosis | Phycomycosis | Mucormycosis | Zygomycosis (& [mucormycosis]) (disorder) | Zygomycosis | Phycomycosis | Zygomycosis (disorder)
+BMGC_DS05451,BMG_DS014413,48813009,Alymphocytosis,,,,,,,C0300946,,,,,Lymphocytopenia | Lymphopenia | Alymphocytosis | Lymphocytopenia (disorder)
+BMGC_DS05452,BMG_DS014414,,,,,,,,,C0300948,,,MONDO:0017607,caudal regression sequence,
+BMGC_DS05453,BMG_DS014423,,,,,,,DOID:3965,Merkel cell carcinoma,C0302182,,,MONDO:0002822,trabecular adenocarcinoma,
+BMGC_DS05454,BMG_DS014426,,,,,,,,,C0302313,,,MONDO:0043731,lytic metastatic bone lesion,
+BMGC_DS05455,BMG_DS014427,75594004;63103006;6400008,Xanthoma,Xanthomatosis,,,,,,C0302314,D014973,MTHU012701,MONDO:0005236,xanthoma,Xanthomatous deposition | Xanthelasma | Xanthoma | Xanthomatous deposition (morphologic abnormality) | Xanthomatosis | Xanthoma | Xanthomatosis (disorder) | Xanthoma of eyelid | Xanthoma of eyelid (disorder)
+BMGC_DS05456,BMG_DS014428,,"Porokeratosis, Linear",Porokeratosis,,,,,,C0302319,D017499,,MONDO:0023246,linear porokeratosis,
+BMGC_DS05457,BMG_DS014429,,,,,,,DOID:7614,meninges sarcoma,C0302327,,,MONDO:0004308,meningeal sarcoma,
+BMGC_DS05458,BMG_DS014433,,,,,,,DOID:14456,Brucella melitensis brucellosis,C0302362,,,MONDO:0001972,Brucella melitensis brucellosis,
+BMGC_DS05459,BMG_DS014434,,,,,,,DOID:14457,Brucella abortus brucellosis,C0302363,,,MONDO:0001973,Brucella abortus brucellosis,
+BMGC_DS05460,BMG_DS014436,,Alcohol Withdrawal Hallucinosis,Alcohol Withdrawal Delirium,,,,,,C0302369,D000430,,,,
+BMGC_DS05461,BMG_DS014441,,,,,,,DOID:2893,cervix carcinoma,C0302592,,,MONDO:0005131,cervical carcinoma,
+BMGC_DS05462,BMG_DS014442,,Fulminant Hepatitis,Massive Hepatic Necrosis,,,,,,C0302809,D047508,,,,
+BMGC_DS05463,BMG_DS014444,,Euthyroid Goiter,,,,,,,C0302859,C562732,138800,MONDO:0007681,"goiter, multinodular 1, with or without Sertoli-Leydig cell tumors",
+BMGC_DS05464,BMG_DS014446,,,,,,,DOID:0060263,porencephaly,C0302892,,,,,
+BMGC_DS05465,BMG_DS014452,53593008;53651004,Pustular folliculitis,,,,,,,C0311217,,,,,Folliculitis decalvans | Folliculitis decalvans (disorder) | Folliculitis depilans | Pustular folliculitis | Pustular folliculitis (disorder)
+BMGC_DS05466,BMG_DS014455,399114005;8753005;202837002;156658000;202847004;156664007;268087008,Frozen shoulder,,FB53.0,Adhesive capsulitis of shoulder,M75.0,DOID:14188,frozen shoulder,C0311223,,,MONDO:0006763,frozen shoulder,"Adhesive capsulitis of shoulder (disorder) | Adhesive capsulitis of shoulder | Duplay's periarthritis syndrome | Pericapsulitis of shoulder | Frozen shoulder | Periarthritis of shoulder | Duplay periarthritis syndrome | Adhesive capsulitis of shoulder | Scapulohumeral fibrositis | Frozen shoulder | Scapulohumeral myofibrosis | Duplay's periarthritis syndrome | Periarthritis of shoulder | Pericapsulitis of shoulder | Adhesive capsulitis of shoulder (disorder) | Shoulder: (frozen) or (adhesive capsulitis) or (bursitis) | Frozen shoulder | Adhesive capsulitis of the shoulder | Adhesive capsulitis shoulder | Adhesive capsulitis of shoulder | Bursitis - shoulder | Bursitis of shoulder | Shoulder: (frozen) or (adhesive capsulitis) or (bursitis) (disorder) | (Shoulder: [syndrome (& [painful arc][rotator cuff])][bicipital tendinit][bursitis][frozen][pericapsulit][adhes capsulit]) or (tendinitis: [subscapular][supraspinat][infraspinat][bicep long head]) | Infraspinatus tendinitis | Bursitis of shoulder | Shoulder syndrome | Painful arc syndr - shoulder | Pericapsulitis of shoulder | Subscapularis tendinitis | Biceps tendinitis (long head) | Pericapsulitis, shoulder | Painful arc syndrome: shoulder | Bursitis - shoulder | Supraspinatus tendinitis | Rotator cuff syndrome | Bicipital tendinitis-shoulder | Adhesive capsulitis of shoulder | Adhesions-capsulitis,shoulder | Frozen shoulder | (Shoulder: [syndrome (& [painful arc][rotator cuff])][bicipital tendinit][bursitis][frozen][pericapsulit][adhes capsulit]) or (tendinitis: [subscapular][supraspinat][infraspinat][bicep long head]) (disorder) | Frozen shoulder | Frozen shoulder (disorder) | Adhesions-capsulitis,shoulder | Shoulder syndrome | Pericapsulitis, shoulder | Bicipital tendinitis-shoulder | Subscapularis tendinitis | Painful arc syndr - shoulder | Frozen shoulder | Pericapsulitis of shoulder | Adhesive capsulitis of shoulder | Rotator cuff syndrome | Supraspinatus tendinitis | Infraspinatus tendinitis | Bursitis of shoulder | Biceps tendinitis (long head) | Painful arc syndrome: shoulder | Bursitis - shoulder | (Shoulder: [syndrome (& [painful arc][rotator cuff])][bicipital tendinit][bursitis][frozen][pericapsulit][adhes capsulit]) or (tendinitis: [subscapular][supraspinat][infraspinat][bicep long head]) | (Shoulder: [syndrome (& [painful arc][rotator cuff])][bicipital tendinit][bursitis][frozen][pericapsulit][adhes capsulit]) or (tendinitis: [subscapular][supraspinat][infraspinat][bicep long head]) (disorder)"
+BMGC_DS05467,BMG_DS014457,204954005;82525005,Congenital cystic kidney disease,,,,,DOID:0050778,Meckel syndrome,C0311245,,,,,Kidney: [congenital cystic disease] or [fibrocystic] or [polycystic] or [sponge] | Congenital cystic disease of kidney | Fibrocystic kidney | Polycystic kidney | Congenital cystic renal disease | Congenital cystic kidney disease | Sponge kidney | Kidney: [congenital cystic disease] or [fibrocystic] or [polycystic] or [sponge] (disorder) | Congenital cystic kidney disease | Multiple congenital cysts of kidney | Congenital polycystic kidney disease | Sponge kidney | PKD - Polycystic kidney disease | Polycystic kidney disease | Congenital cystic disease of kidney | Congenital cyst of kidney | PCK - Polycystic kidney disease | Congenital cystic kidney disease (disorder)
+BMGC_DS05468,BMG_DS014458,,,,,,,DOID:0111716,cryptophthalmia,C0311249,,,MONDO:0020153,cryptophthalmia,
+BMGC_DS05469,BMG_DS014459,,,,,,,DOID:11211,buphthalmos,C0311251,,,,,
+BMGC_DS05470,BMG_DS014460,266448009;111354009,Chronic mesenteric ischemia,,,,,DOID:8633,chronic intestinal vascular insufficiency,C0311262,,,MONDO:0004622,chronic intestinal vascular insufficiency,Chronic mesenteric ischemia | Chronic mesenteric ischaemia | Chronic mesenteric ischaemia (disorder) | Chronic vascular insufficiency of intestine | Chronic intestinal ischemic syndrome | Chronic intestinal vascular insufficiency | Chronic intestinal ischaemia | Chronic mesenteric ischaemia | Chronic intestinal ischaemic syndrome | Chronic intestinal ischemia | Chronic mesenteric ischemia | Chronic vascular insufficiency of intestine (disorder) | CMI - Chronic mesenteric ischemia | CMI - Chronic mesenteric ischaemia
+BMGC_DS05471,BMG_DS014463,26918003,Ascending cholangitis,,,,K83.09,DOID:14270,ascending cholangitis,C0311273,,,MONDO:0001929,ascending cholangitis,Ascending cholangitis | Ascending cholangitis (disorder)
+BMGC_DS05472,BMG_DS014465,84241008,Lipoid dermatoarthritis,,,,E78.81,DOID:11824,multicentric reticulohistiocytosis,C0311284,,,MONDO:0015347,multicentric reticulohistiocytosis,Lipoid dermatoarthritis | Multicentric reticulohistiocytosis | Nicolau-Balus syndrome | Lipoid dermatoarthritis (disorder)
+BMGC_DS05473,BMG_DS014475,,Grand Mal Status Epilepticus,Status Epilepticus,,,,,,C0311335,D013226,,,,
+BMGC_DS05474,BMG_DS014477,,,,,,,DOID:11105,fundus albipunctatus,C0311338,,136880,MONDO:0007639,fundus albipunctatus,
+BMGC_DS05475,BMG_DS014487,19267009,Lupus anticoagulant disorder,,,,,,,C0311370,,,,,Lupus anticoagulant disorder | Lupus anticoagulant inhibitor syndrome | SLE inhibitor syndrome | Lupus anticoagulant disorder (disorder) | Lupus anticoagulant
+BMGC_DS05476,BMG_DS014491,360427001;73034009;240373006;371423007,Isosporiasis,Isosporiasis,1A33.Z,"Cystoisosporiasis, unspecified",A07.3,DOID:2112,cystoisosporiasis,C0311386,D021865,,MONDO:0018769,isosporiasis,Coccidial enteritis | Intestinal coccidiosis | Isosporiasis | Intestinal coccidiosis (disorder) | Isosporiasis | Isosporiasis (disorder) | Isosporosis | Isosporiasis | Isosporiasis (disorder) | Isosporiasis (disorder) | Isosporiasis | Isosporosis
+BMGC_DS05477,BMG_DS014493,154388003,Nonspecific urethritis,,,,,DOID:1343,urethritis,C0311389,,,,,Nonspecific urethritis | Nonspecific urethritis (disorder)
+BMGC_DS05478,BMG_DS014494,,,,,,,,,C0311468,,,MONDO:0024288,hyperbilirubinemia,
+BMGC_DS05479,BMG_DS014500,,,,,,,,,C0332878,,,MONDO:0022823,congenital contractures,
+BMGC_DS05480,BMG_DS014521,,,,,,,,,C0333355,,,MONDO:0020579,mucositis,
+BMGC_DS05481,BMG_DS014538,,,,,,,DOID:6755,amyloid tumor,C0333572,,,,,
+BMGC_DS05482,BMG_DS014544,,Focal Nodular Hyperplasia,Focal Nodular Hyperplasia,,,,,,C0333980,D020518,,,,
+BMGC_DS05483,BMG_DS014546,,,,,,,DOID:172,clear cell acanthoma,C0333992,,,MONDO:0002086,clear cell acanthoma,
+BMGC_DS05484,BMG_DS014553,,,,,,,DOID:6945,inverted follicular keratosis,C0334019,,,MONDO:0006563,inverted follicular keratosis,
+BMGC_DS05485,BMG_DS014557,,,,,,,DOID:7334,nephrogenic adenoma,C0334039,,,MONDO:0004191,nephrogenic adenoma,
+BMGC_DS05486,BMG_DS014558,404074003;71304002,Osteoma cutis,,,,,DOID:0111535,progressive osseous heteroplasia,C0334041,,166350,MONDO:0008153,progressive osseous heteroplasia,Osteoma cutis (disorder) | Osteoma cutis | Osteoma cutis | Cutaneous ossification | Osteosis cutis | Osteodermia | Osteoma cutis (morphologic abnormality)
+BMGC_DS05487,BMG_DS014562,35813005,"Fibrocystic change, proliferative type with atypia",,,,,DOID:3274,proliferative type fibrocystic change of breast,C0334056,,,,,"Fibrocystic change, proliferative type with atypia | Fibrocystic change, proliferative type with atypia (morphologic abnormality)"
+BMGC_DS05488,BMG_DS014564,,Epidermal Nevus,,,,,DOID:0111162,epidermal nevus,C0334082,C580062,162900,MONDO:0008093,"nevus, epidermal",
+BMGC_DS05489,BMG_DS014566,403546006;86970009,Lymphangiomatosis,,,,,,,C0334102,,,,,Lymphangiomatosis (disorder) | Lymphangiomatosis | Lymphangiomatosis | Lymphangiomatosis (morphologic abnormality)
+BMGC_DS05490,BMG_DS014569,,,,,,,,,C0334121,,,MONDO:0015798,inflammatory myofibroblastic tumor,
+BMGC_DS05491,BMG_DS014572,,"Histiocytosis, Familial Lipochrome",,,,,,,C0334125,C562738,235900,MONDO:0009347,familial lipochrome histiocytosis,
+BMGC_DS05492,BMG_DS014578,,,,,,,DOID:2705,malignant giant cell tumor,C0334229,,,MONDO:0002402,malignant giant cell tumor,
+BMGC_DS05493,BMG_DS014581,,,,,,,DOID:5662,pleomorphic carcinoma,C0334233,,,MONDO:0003573,pleomorphic carcinoma,
+BMGC_DS05494,BMG_DS014582,,,,,,,DOID:0050685,small cell carcinoma,C0334239,,,MONDO:0000402,small cell carcinoma,
+BMGC_DS05495,BMG_DS014583,,,,,,,DOID:3177,verrucous papilloma,C0334243,,,MONDO:0002535,verrucous papilloma,
+BMGC_DS05496,BMG_DS014584,,,,,,,DOID:4385,papillary squamous carcinoma,C0334244,,,MONDO:0002979,papillary squamous carcinoma,
+BMGC_DS05497,BMG_DS014587,,,,,,,DOID:5521,keratinizing squamous cell carcinoma,C0334247,,,MONDO:0005056,keratinizing squamous cell carcinoma,
+BMGC_DS05498,BMG_DS014588,,,,,,,DOID:5524,adenoid squamous cell carcinoma,C0334250,,,,,
+BMGC_DS05499,BMG_DS014589,,,,,,,DOID:5660,lymphoepithelioma-like carcinoma,C0334254,,,MONDO:0003572,nasopharyngeal type undifferentiated carcinoma,
+BMGC_DS05500,BMG_DS014590,,,,,,,DOID:4300,superficial basal cell carcinoma,C0334256,,,MONDO:0002954,superficial multifocal basal cell carcinoma,
+BMGC_DS05501,BMG_DS014592,,,,,,,DOID:7039,Borst-Jadassohn intraepidermal carcinoma,C0334260,,,,,
+BMGC_DS05502,BMG_DS014594,,,,,,,DOID:2671,transitional cell carcinoma,C0334265,,,MONDO:0037254,transitional cell neoplasm,
+BMGC_DS05503,BMG_DS014595,,,,,,,DOID:2670,transitional papilloma,C0334266,,,MONDO:0005605,transitional cell papilloma,
+BMGC_DS05504,BMG_DS014596,,,,,,,DOID:4630,inverted transitional papilloma,C0334269,,,,,
+BMGC_DS05505,BMG_DS014597,,,,,,,DOID:4003,Schneiderian carcinoma,C0334270,,,MONDO:0002831,non-keratinizing sinonasal squamous cell carcinoma,
+BMGC_DS05506,BMG_DS014598,,,,,,,DOID:4014,sarcomatoid transitional cell carcinoma,C0334271,,,MONDO:0002837,sarcomatoid transitional cell carcinoma,
+BMGC_DS05507,BMG_DS014599,,,,,,,DOID:7173,cloacogenic carcinoma,C0334273,,,MONDO:0004129,cloacogenic carcinoma,
+BMGC_DS05508,BMG_DS014600,,,,,,,DOID:4012,papillary transitional carcinoma,C0334274,,,MONDO:0006350,papillary transitional cell carcinoma,
+BMGC_DS05509,BMG_DS014601,,,,,,,DOID:4943,adenocarcinoma in situ,C0334276,,,MONDO:0003218,adenocarcinoma in situ,
+BMGC_DS05510,BMG_DS014603,,,,,,,DOID:6217,gastric diffuse adenocarcinoma,C0334280,,,MONDO:0021652,diffuse type adenocarcinoma,
+BMGC_DS05511,BMG_DS014604,,,,,,,DOID:5384,bile duct cystadenoma,C0334285,,,MONDO:0003420,bile duct cystadenoma,
+BMGC_DS05512,BMG_DS014605,,,,,,,DOID:4075,bile duct cystadenocarcinoma,C0334286,,,MONDO:0002868,bile duct mucinous cystic neoplasm with an associated invasive carcinoma,
+BMGC_DS05513,BMG_DS014606,,,,,,,DOID:5015,fibrolamellar carcinoma,C0334287,,,MONDO:0006210,fibrolamellar hepatocellular carcinoma,
+BMGC_DS05514,BMG_DS014610,,,,,,,DOID:8003,alveoli adenoma,C0334303,,,MONDO:0004428,alveoli adenoma,
+BMGC_DS05515,BMG_DS014611,,,,,,,DOID:4917,villous adenocarcinoma,C0334306,,,MONDO:0003204,villous adenocarcinoma,
+BMGC_DS05516,BMG_DS014613,,,,,,,DOID:7179,mixed eosinophil-basophil adenoma,C0334312,,,MONDO:0004133,pituitary gland mixed eosinophil-basophil adenoma,
+BMGC_DS05517,BMG_DS014614,,,,,,,DOID:4915,basophilic adenocarcinoma,C0334314,,,,,
+BMGC_DS05518,BMG_DS014615,,,,,,,DOID:5390,clear cell adenoma,C0334315,,,MONDO:0003426,clear cell adenoma,
+BMGC_DS05519,BMG_DS014616,,,,,,,DOID:5482;DOID:5477,clear cell adenofibroma | cystadenofibroma,C0334317,,,MONDO:0003460,clear cell adenofibroma,
+BMGC_DS05520,BMG_DS014617,,,,,,,DOID:5658,lipid-rich carcinoma,C0334318,,,MONDO:0003570,lipid-rich carcinoma,
+BMGC_DS05521,BMG_DS014618,,,,,,,DOID:0081028,glycogen-rich carcinoma,C0334319,,,MONDO:0045055,glycogen-rich carcinoma,
+BMGC_DS05522,BMG_DS014619,,,,,,,DOID:7607,chief cell adenoma,C0334320,,,MONDO:0004302,chief cell adenoma,
+BMGC_DS05523,BMG_DS014620,,,,,,,DOID:5401,water-clear cell adenoma,C0334321,,,MONDO:0003433,water-clear cell adenoma,
+BMGC_DS05524,BMG_DS014621,,,,,,,DOID:4468,clear cell adenocarcinoma,C0334322,,,,,
+BMGC_DS05525,BMG_DS014622,,,,,,,DOID:5385,mixed cell adenoma,C0334323,,,MONDO:0003421,mixed cell adenoma,
+BMGC_DS05526,BMG_DS014623,,,,,,,DOID:5398,lipoadenoma,C0334325,,,MONDO:0003431,lipoadenoma,
+BMGC_DS05527,BMG_DS014624,,,,,,,DOID:3964,trabecular follicular adenocarcinoma,C0334327,,,MONDO:0002821,trabecular follicular adenocarcinoma,
+BMGC_DS05528,BMG_DS014625,,,,,,,DOID:8102,fetal adenoma,C0334328,,,MONDO:0004460,thyroid gland fetal adenoma,
+BMGC_DS05529,BMG_DS014626,,,,,,,DOID:8419,colloid adenoma,C0334329,,,MONDO:0004558,thyroid gland macrofollicular adenoma,
+BMGC_DS05530,BMG_DS014627,,,,,,,DOID:5914,diffuse sclerosing papillary thyroid carcinoma,C0334330,,,MONDO:0003701,thyroid gland diffuse sclerosing papillary carcinoma,
+BMGC_DS05531,BMG_DS014629,,,,,,,DOID:3895,apocrine adenoma,C0334345,,,MONDO:0002804,apocrine adenoma,
+BMGC_DS05532,BMG_DS014630,,,,,,,DOID:4933,apocrine carcinoma,C0334346,,,MONDO:0003214,apocrine adenocarcinoma,
+BMGC_DS05533,BMG_DS014631,,,,,,,DOID:5444,spiradenoma,C0334347,,,MONDO:0003448,benign spiradenoma,
+BMGC_DS05534,BMG_DS014632,,,,,,,DOID:5439,papillary hidradenoma,C0334348,,,MONDO:0003446,papillary hidradenoma,
+BMGC_DS05535,BMG_DS014633,,,,,,,DOID:5446,eccrine papillary adenoma,C0334350,,,MONDO:0003450,eccrine papillary adenoma,
+BMGC_DS05536,BMG_DS014634,,,,,,,DOID:7549,ceruminoma,C0334352,,,MONDO:0004276,ceruminoma,
+BMGC_DS05537,BMG_DS014635,,,,,,,DOID:6446,ceruminous adenocarcinoma,C0334353,,,MONDO:0003880,ceruminous carcinoma,
+BMGC_DS05538,BMG_DS014637,,,,,,,DOID:2614,serous surface papilloma,C0334360,,,MONDO:0002362,serous surface papilloma,
+BMGC_DS05539,BMG_DS014638,,,,,,,DOID:3030,mucinous adenocarcinoma,C0334368,,,MONDO:0020596,mucin-producing carcinoma,
+BMGC_DS05540,BMG_DS014640,,,,,,,DOID:4922,breast secretory carcinoma,C0334371,,,MONDO:0003208,breast secretory carcinoma,
+BMGC_DS05541,BMG_DS014641,,,,,,,DOID:2682,intracystic papillary adenoma,C0334374,,,MONDO:0002388,intracystic papillary adenoma,
+BMGC_DS05542,BMG_DS014645,,,,,,,DOID:657,adenoma,C0334389,,,,,
+BMGC_DS05543,BMG_DS014646,,,,,,,DOID:5309,epithelial-myoepithelial carcinoma,C0334392,,,MONDO:0003389,epithelial-myoepithelial carcinoma,
+BMGC_DS05544,BMG_DS014647,,,,,,,DOID:5524,adenoid squamous cell carcinoma,C0334393,,,,,
+BMGC_DS05545,BMG_DS014648,,,,,,,DOID:2999,granulosa cell tumor,C0334401,,,,,
+BMGC_DS05546,BMG_DS014649,,,,,,,DOID:6032,juvenile type testicular granulosa cell tumor,C0334403,,,,,
+BMGC_DS05547,BMG_DS014652,,,,,,,DOID:2696,Leydig cell tumor,C0334410,,,MONDO:0000377,malignant Leydig cell tumor,
+BMGC_DS05548,BMG_DS014657,,,,,,,DOID:2436,glomangioma,C0334421,,,MONDO:0002299,glomangioma,
+BMGC_DS05549,BMG_DS014658,,,,,,,DOID:8020,glomangiomyoma,C0334422,,,MONDO:0024323,glomangiomyoma,
+BMGC_DS05550,BMG_DS014659,,,,,,,DOID:10047,nodular malignant melanoma,C0334424,,,MONDO:0000930,nodular malignant melanoma,
+BMGC_DS05551,BMG_DS014660,,,,,,,DOID:10044,balloon cell malignant melanoma,C0334426,,,MONDO:0000929,balloon cell malignant melanoma,
+BMGC_DS05552,BMG_DS014662,,,,,,,DOID:4360,epithelioid cell melanoma,C0334443,,,MONDO:0002973,epithelioid cell melanoma,
+BMGC_DS05553,BMG_DS014663,,,,,,,DOID:3162,malignant spindle cell melanoma,C0334444,,,MONDO:0006427,spindle cell melanoma,
+BMGC_DS05554,BMG_DS014665,,,,,,,DOID:7615,sarcomatosis,C0334451,,,MONDO:0004309,sarcomatosis,
+BMGC_DS05555,BMG_DS014666,,,,,,,DOID:8418,congenital fibrosarcoma,C0334459,,,MONDO:0004557,congenital fibrosarcoma,
+BMGC_DS05556,BMG_DS014668,,,,,,,DOID:1907,malignant fibrous histiocytoma,C0334463,,,MONDO:0002142,undifferentiated pleomorphic sarcoma,
+BMGC_DS05557,BMG_DS014670,,,,,,,DOID:5704,sclerosing liposarcoma,C0334469,,,MONDO:0003595,sclerosing liposarcoma,
+BMGC_DS05558,BMG_DS014671,,,,,,,DOID:5692,cellular myxoid liposarcoma,C0334471,,,MONDO:0005238,round cell liposarcoma,
+BMGC_DS05559,BMG_DS014672,,,,,,,DOID:5703,mixed liposarcoma,C0334472,,,MONDO:0003594,mixed liposarcoma,
+BMGC_DS05560,BMG_DS014673,,,,,,,DOID:7014,infiltrating lipoma,C0334473,,,MONDO:0004075,infiltrating lipoma,
+BMGC_DS05561,BMG_DS014674,,,,,,,DOID:10184,spindle cell lipoma,C0334474,,,MONDO:0000962,spindle cell lipoma,
+BMGC_DS05562,BMG_DS014675,,,,,,,DOID:5139,cellular leiomyoma,C0334477,,,MONDO:0003296,cellular leiomyoma,
+BMGC_DS05563,BMG_DS014676,,,,,,,DOID:5127,bizarre leiomyoma,C0334478,,,MONDO:0003288,bizarre leiomyoma,
+BMGC_DS05564,BMG_DS014677,,,,,,,DOID:3250,pleomorphic rhabdomyosarcoma,C0334480,,,MONDO:0017386,pleomorphic rhabdomyosarcoma,
+BMGC_DS05565,BMG_DS014678,,,,,,,DOID:4065,mixed type rhabdomyosarcoma,C0334481,,,,,
+BMGC_DS05566,BMG_DS014680,,,,,,,DOID:4880,kidney clear cell sarcoma,C0334488,,,MONDO:0005006,clear cell sarcoma of kidney,
+BMGC_DS05567,BMG_DS014681,,,,,,,DOID:6823,pancreatoblastoma,C0334489,,,MONDO:0019035,pancreatoblastoma,
+BMGC_DS05568,BMG_DS014683,,,,,,,DOID:5758,malignant mesenchymoma,C0334492,,,MONDO:0003633,malignant mesenchymoma,
+BMGC_DS05569,BMG_DS014684,,,,,,,DOID:4217,malignant ovarian Brenner tumor,C0334495,,,MONDO:0002920,malignant ovarian Brenner tumor,
+BMGC_DS05570,BMG_DS014685,,,,,,,DOID:2656,breast intracanalicular fibroadenoma,C0334496,,,MONDO:0002377,breast intracanalicular fibroadenoma,
+BMGC_DS05571,BMG_DS014686,,,,,,,DOID:2639,breast pericanalicular fibroadenoma,C0334497,,,MONDO:0002371,breast pericanalicular fibroadenoma,
+BMGC_DS05572,BMG_DS014688,,,,,,,DOID:2700,mucinous adenofibroma,C0334499,,,MONDO:0002398,mucinous adenofibroma,
+BMGC_DS05573,BMG_DS014690,,,,,,,DOID:5487,spindle cell synovial sarcoma,C0334505,,,MONDO:0003466,spindle cell synovial sarcoma,
+BMGC_DS05574,BMG_DS014691,,,,,,,DOID:5494,epithelioid cell synovial sarcoma,C0334506,,,MONDO:0003469,epithelioid cell synovial sarcoma,
+BMGC_DS05575,BMG_DS014692,,,,,,,DOID:5492,biphasic synovial sarcoma,C0334507,,,MONDO:0003468,biphasic synovial sarcoma,
+BMGC_DS05576,BMG_DS014693,,,,,,,DOID:2653,benign fibrous mesothelioma,C0334511,,,,,
+BMGC_DS05577,BMG_DS014694,,,,,,,DOID:4488,sarcomatoid mesothelioma,C0334513,,,MONDO:0006407,sarcomatoid mesothelioma,
+BMGC_DS05578,BMG_DS014695,,,,,,,DOID:4486,malignant biphasic mesothelioma,C0334515,,,MONDO:0006109,malignant biphasic mesothelioma,
+BMGC_DS05579,BMG_DS014696,,,,,,,DOID:5834,spermatocytoma,C0334517,,,MONDO:0020513,spermatocytic seminoma,
+BMGC_DS05580,BMG_DS014698,,,,,,,DOID:5563,malignant teratoma,C0334520,,,MONDO:0024746,immature teratoma,
+BMGC_DS05581,BMG_DS014699,,,,,,,DOID:7202,intermediate malignant teratoma,C0334522,,,MONDO:0004140,intermediate malignant teratoma,
+BMGC_DS05582,BMG_DS014701,,,,,,,DOID:3306,mixed germ cell cancer,C0334524,,,MONDO:0015864,mixed germ cell tumor,
+BMGC_DS05583,BMG_DS014702,,,,,,,DOID:5208,malignant struma ovarii,C0334525,,,MONDO:0003332,malignant struma ovarii,
+BMGC_DS05584,BMG_DS014703,,,,,,,,,C0334529,,,MONDO:0016786,partial hydatidiform mole,
+BMGC_DS05585,BMG_DS014707,,,,,,,DOID:11294,arteriovenous malformation,C0334533,,,MONDO:0001256,arteriovenous hemangioma/malformation,
+BMGC_DS05586,BMG_DS014709,,,,,,,DOID:470,verrucous keratotic hemangioma,C0334540,,,MONDO:0018734,verrucous hemangioma,
+BMGC_DS05587,BMG_DS014710,,,,,,,,,C0334542,,234820,MONDO:0009330,"hemangiopericytoma, malignant",
+BMGC_DS05588,BMG_DS014712,,,,,,,DOID:7542,osteosarcoma arising in bone Paget's disease,C0334546,,,MONDO:0004275,osteosarcoma arising in bone Paget disease,
+BMGC_DS05589,BMG_DS014713,,,,,,,DOID:2601,juxtacortical chondroma,C0334548,,,MONDO:0002359,periosteal chondroma,
+BMGC_DS05590,BMG_DS014714,,,,,,,DOID:5866,juxtacortical chondrosarcoma,C0334549,,,MONDO:0003680,periosteal chondrosarcoma,
+BMGC_DS05591,BMG_DS014715,,,,,,,DOID:5861,myxoid chondrosarcoma,C0334551,,,MONDO:0003681,myxoid chondrosarcoma,
+BMGC_DS05592,BMG_DS014716,,,,,,,DOID:4719,bone giant cell sarcoma,C0334552,,,MONDO:0006287,malignancy in giant cell tumor of bone,
+BMGC_DS05593,BMG_DS014718,,,,,,,DOID:5638,malignant giant cell tumor of soft parts,C0334554,,,MONDO:0003561,malignant giant cell tumor of soft parts,
+BMGC_DS05594,BMG_DS014719,,,,,,,DOID:2775;DOID:2776,adamantinoma | long bone adamantinoma,C0334556,,102660,MONDO:0002422,adamantinoma,
+BMGC_DS05595,BMG_DS014722,,,,,,,DOID:6128,gliomatosis cerebri,C0334576,,,MONDO:0016683,gliomatosis cerebri,
+BMGC_DS05596,BMG_DS014723,,,,,,,DOID:5505,papillary ependymoma,C0334578,,,MONDO:0003475,papillary ependymoma,
+BMGC_DS05597,BMG_DS014724,,,,,,,DOID:3078,anaplastic astrocytoma,C0334579,,,MONDO:0016684,anaplastic astrocytoma,
+BMGC_DS05598,BMG_DS014725,,,,,,,DOID:7008,protoplasmic astrocytoma,C0334580,,,MONDO:0016687,protoplasmic astrocytoma,
+BMGC_DS05599,BMG_DS014726,,,,,,,DOID:7005,gemistocytic astrocytoma,C0334581,,,MONDO:0016689,gemistocytic astrocytoma,
+BMGC_DS05600,BMG_DS014727,,,,,,,DOID:6726,fibrillary astrocytoma,C0334582,,,MONDO:0016688,fibrillary astrocytoma,
+BMGC_DS05601,BMG_DS014728,,,,,,,DOID:4851,pilocytic astrocytoma,C0334583,,,MONDO:0016691,pilocytic astrocytoma,
+BMGC_DS05602,BMG_DS014729,,,,,,,DOID:4852,pleomorphic xanthoastrocytoma,C0334586,,,MONDO:0016690,pleomorphic xanthoastrocytoma,
+BMGC_DS05603,BMG_DS014730,,,,,,,DOID:7305,astroblastoma,C0334587,,,MONDO:0016707,astroblastoma,
+BMGC_DS05604,BMG_DS014731,,,,,,,DOID:3074,giant cell glioblastoma,C0334588,,,MONDO:0016682,giant cell glioblastoma,
+BMGC_DS05605,BMG_DS014732,,,,,,,,,C0334590,,,MONDO:0016696,anaplastic oligodendroglioma,
+BMGC_DS05606,BMG_DS014734,,,,,,,DOID:2669,Pacinian tumor,C0334599,,,MONDO:0002383,Pacinian tumor,
+BMGC_DS05607,BMG_DS014735,,,,,,,DOID:7212,meningothelial meningioma,C0334605,,,MONDO:0004145,meningothelial meningioma,
+BMGC_DS05608,BMG_DS014736,,,,,,,DOID:7211,fibrous meningioma,C0334606,,,MONDO:0004144,fibrous meningioma,
+BMGC_DS05609,BMG_DS014737,,,,,,,DOID:7210,psammomatous meningioma,C0334607,,,MONDO:0004143,psammomatous meningioma,
+BMGC_DS05610,BMG_DS014738,,,,,,,DOID:6548,angiomatous meningioma,C0334608,,,MONDO:0003918,angiomatous meningioma,
+BMGC_DS05611,BMG_DS014739,,,,,,,DOID:7213,transitional meningioma,C0334611,,,MONDO:0004146,transitional meningioma,
+BMGC_DS05612,BMG_DS014740,,,,,,,DOID:7613,sarcomatosis of the meninges,C0334612,,,MONDO:0004307,sarcomatosis of the meninges,
+BMGC_DS05613,BMG_DS014741,,,,,,,DOID:6707,malignant triton tumor,C0334616,,,MONDO:0016757,malignant triton tumor,
+BMGC_DS05614,BMG_DS014742,,,,,,,DOID:5042,malignant granular cell myoblastoma,C0334618,,,MONDO:0003252,granular cell cancer,
+BMGC_DS05615,BMG_DS014743,,,,,,,,,C0334633,,,MONDO:0000432,lymphoplasmacytic lymphoma,
+BMGC_DS05616,BMG_DS014744,,,,,,,,,C0334660,,,MONDO:0020324,intravascular large B-cell lymphoma,
+BMGC_DS05617,BMG_DS014745,,,,,,,,,C0334663,,,MONDO:0019479,histiocytic sarcoma,
+BMGC_DS05618,BMG_DS014746,,,,,,,DOID:3664,mast cell neoplasm,C0334664,,,MONDO:0002724,mast cell neoplasm,
+BMGC_DS05619,BMG_DS014749,,,,,,,DOID:2697,renal adenoma,C0334684,,,MONDO:0002395,renal adenoma,
+BMGC_DS05620,BMG_DS014750,,,,,,,DOID:5166,endometrial stromal tumor,C0334695,,,MONDO:0003311,endometrial stromal tumor,
+BMGC_DS05621,BMG_DS014751,,,,,,,DOID:4838,myoepithelial carcinoma,C0334699,,,MONDO:0003158,malignant myoepithelioma,
+BMGC_DS05622,BMG_DS014752,,,,,,,DOID:7007,childhood cerebral astrocytoma,C0338070,,,MONDO:0004071,childhood cerebral astrocytoma,
+BMGC_DS05623,BMG_DS014753,,,,,,,DOID:5715,functionless pituitary adenoma,C0338078,,,MONDO:0017825,silent pituitary adenoma,
+BMGC_DS05624,BMG_DS014754,,,,,,,DOID:234,colon adenocarcinoma,C0338106,,,MONDO:0002271,colon adenocarcinoma,
+BMGC_DS05625,BMG_DS014755,,,,,,,DOID:5165,uterine corpus sarcoma,C0338113,,,MONDO:0005210,uterine corpus sarcoma,
+BMGC_DS05626,BMG_DS014767,,"Meningitis, Escherichia coli","Meningitis, Escherichia coli",,,,,,C0338395,D020814,,MONDO:0006753,Escherichia coli meningitis,
+BMGC_DS05627,BMG_DS014768,302877009,Proteus meningitis,,,,,,,C0338396,,,,,Proteus meningitis | Proteus meningitis (disorder)
+BMGC_DS05628,BMG_DS014785,,"Encephalitis, Acute Necrotizing","Leukoencephalitis, Acute Hemorrhagic",,,,DOID:5222,acute necrotizing encephalitis,C0338418,D004684,,MONDO:0003336,acute necrotizing encephalitis,
+BMGC_DS05629,BMG_DS014794,,Limbic Encephalitis,Limbic Encephalitis,,,,DOID:0080741,limbic encephalitis,C0338430,D020363,,MONDO:0015588,limbic encephalitis,
+BMGC_DS05630,BMG_DS014799,230215006,Neurocysticercosis,Neurocysticercosis,,,,,,C0338437,D020019,,,,Cerebral cysticercosis | Cerebral cysticercosis (disorder)
+BMGC_DS05631,BMG_DS014809,230270009,Frontotemporal dementia,,8E4Y,Other specified disorders of the nervous system,G31.0,DOID:0060672,Grn-related frontotemporal lobar degeneration with Tdp43 inclusions,C0338451,,MTHU003256,MONDO:0017276,frontotemporal dementia,Frontotemporal dementia | Frontotemporal dementia (disorder)
+BMGC_DS05632,BMG_DS014818,,,,,,,,,C0338462,,600274,MONDO:0010857,semantic dementia,
+BMGC_DS05633,BMG_DS014822,,"Tic Disorders, Vocal",Tic Disorders,,,,,,C0338468,D013981,,,,
+BMGC_DS05634,BMG_DS014825,,Neuroaxonal Dystrophies,Neuroaxonal Dystrophies,,,,DOID:2367,neuroaxonal dystrophy,C0338473,D019150,,MONDO:0002283,neuroaxonal dystrophy,
+BMGC_DS05635,BMG_DS014827,,Idiopathic Myoclonic Epilepsy,"Epilepsies, Myoclonic",,,,,,C0338478,D004831,,,,
+BMGC_DS05636,BMG_DS014828,,Symptomatic Myoclonic Epilepsy,"Epilepsies, Myoclonic",,,,,,C0338479,D004831,,,,
+BMGC_DS05637,BMG_DS014829,,Common Migraine,Migraine without Aura,,,,DOID:12783,migraine without aura,C0338480,D020326,,MONDO:0100431,migraine without aura,
+BMGC_DS05638,BMG_DS014831,,Migraine with Prolonged Aura,Migraine with Aura,,,,,,C0338483,D020325,,,,
+BMGC_DS05639,BMG_DS014832,,Familial Hemiplegic Migraine,Migraine with Aura,,,,,,C0338484,D020325,,MONDO:0000700,familial hemiplegic migraine,
+BMGC_DS05640,BMG_DS014833,,Migraine Aura without Headache,Migraine with Aura,,,,,,C0338486,D020325,,,,
+BMGC_DS05641,BMG_DS014835,230466004,Alternating hemiplegia of childhood,,,,,DOID:0050635,alternating hemiplegia of childhood,C0338488,C536589,,MONDO:0016241,alternating hemiplegia of childhood,Alternating hemiplegia of childhood | Alternating hemiplegia of childhood (disorder)
+BMGC_DS05642,BMG_DS014836,,Status Migrainosus,Migraine Disorders,,,,,,C0338489,D008881,,,,
+BMGC_DS05643,BMG_DS014838,,"Sleep Apnea, Mixed Central and Obstructive",Sleep Apnea Syndromes,,,,DOID:0080302,mixed sleep apnea,C0338495,D012891,,MONDO:0024358,complex sleep apnea,
+BMGC_DS05644,BMG_DS014844,,Optic Nerve Hypoplasia,Optic Nerve Hypoplasia,,,,DOID:0111531,bilateral optic nerve hypoplasia,C0338502,D000080344,,,,
+BMGC_DS05645,BMG_DS014845,,Septo-Optic Dysplasia,Septo-Optic Dysplasia,,,,DOID:0060857,septooptic dysplasia,C0338503,D025962,182230,MONDO:0008428,septooptic dysplasia,
+BMGC_DS05646,BMG_DS014849,,Optic Atrophy 1,"Optic Atrophy, Autosomal Dominant",,,,,,C0338508,D029241,165500,MONDO:0008134,"autosomal dominant optic atrophy, classic form",
+BMGC_DS05647,BMG_DS014873,,Ulnar Neuritis,Ulnar Neuropathies,,,,,,C0338538,D020424,,,,
+BMGC_DS05648,BMG_DS014888,192759008,Cerebral venous sinus thrombosis,,,,,,,C0338573,,,,,Cerebral venous sinus thrombosis | Cerebral venous sinus thrombosis (disorder) | Thrombosis of intracranial venous sinus
+BMGC_DS05649,BMG_DS014890,,Sagittal Sinus Thrombosis,Sagittal Sinus Thrombosis,,,,DOID:3576,sagittal sinus thrombosis,C0338575,D020225,,MONDO:0002695,sagittal sinus thrombosis,
+BMGC_DS05650,BMG_DS014895,,Sporadic Cerebral Amyloid Angiopathy,Cerebral Amyloid Angiopathy,,,,,,C0338582,D016657,,,,
+BMGC_DS05651,BMG_DS014896,230729006;720626009,Dissection of carotid artery,,,,I77.71,DOID:9348,carotid artery dissection,C0338585,,,MONDO:0004763,carotid artery dissection,Carotid artery dissection | Carotid artery dissection (disorder) | Dissection of carotid artery | Dissection of carotid artery (disorder) | Dissection of carotid artery | Carotid artery dissection
+BMGC_DS05652,BMG_DS014902,,,,,,,DOID:13027,transient global amnesia,C0338591,,,MONDO:0001617,transient global amnesia,
+BMGC_DS05653,BMG_DS014905,192959001;230773005,Spastic cerebral palsy,,,,,,,C0338596,,MTHU033921,MONDO:0000396,spastic cerebral palsy,Spastic cerebral palsy | Spastic cerebral palsy (disorder) | Spastic cerebral palsy | Spastic cerebral palsy (disorder) | Pyramidal cerebral palsy | Congenital spastic paralysis | Spastic infantile paralysis | Little's disease | Infantile spastic cerebral palsy | Congenital spastic cerebral palsy
+BMGC_DS05654,BMG_DS014923,,"Catatonia, Organic",Catatonia,,,,,,C0338650,D002389,,,,
+BMGC_DS05655,BMG_DS014943,,,,,,,,,C0338908,,,MONDO:0041086,mixed anxiety and depressive disorder,
+BMGC_DS05656,BMG_DS014977,,Blepharochalasis And Double Lip,,,,,,,C0339085,C562742,109900,MONDO:0007198,Ascher syndrome,
+BMGC_DS05657,BMG_DS014984,,,,,,,DOID:10040,malignant eyelid melanoma,C0339116,,,MONDO:0000928,eyelid melanoma,
+BMGC_DS05658,BMG_DS014987,,,,,,,DOID:1822,secondary lacrimal atrophy,C0339121,,,MONDO:0002124,secondary lacrimal atrophy,
+BMGC_DS05659,BMG_DS014988,,,,,,,DOID:294,lacrimal gland cancer,C0339124,,,MONDO:0021222,lacrimal gland neoplasm,
+BMGC_DS05660,BMG_DS014991,302900006,Acute inflammation of lacrimal passages,,,,,DOID:6970,acute inflammation of lacrimal passage,C0339129,,,MONDO:0004055,acute inflammation of lacrimal passage,Acute inflammation of lacrimal passages | Acute inflammation of lacrimal passages (disorder)
+BMGC_DS05661,BMG_DS014992,84399007,Acute lacrimal canaliculitis,,,,H04.33,DOID:6969,acute canaliculitis,C0339130,,,MONDO:0004054,acute canaliculitis,Acute lacrimal canaliculitis | Acute lacrimal canaliculitis (disorder) | Acute canaliculitis
+BMGC_DS05662,BMG_DS014999,,Graves Ophthalmopathy,Graves Ophthalmopathy,,,,DOID:0081120,Graves ophthalmopathy,C0339143,D049970,,,,
+BMGC_DS05663,BMG_DS015012,231862003,Fungal conjunctivitis,,,,,,,C0339170,,,,,Fungal conjunctivitis | Fungal conjunctivitis (disorder)
+BMGC_DS05664,BMG_DS015031,231901007,Neuropathic corneal ulcer,,,,,,,C0339223,,,,,Neuropathic corneal ulcer | Neuroparalytic keratitis | Neuropathic corneal ulcer (disorder) | Neurotrophic corneal ulcer
+BMGC_DS05665,BMG_DS015051,,"Corneal dystrophy, Lattice type 3",,,,,DOID:0060449,gelatinous drop-like corneal dystrophy,C0339273,C535480,204870,MONDO:0008777,gelatinous drop-like corneal dystrophy,
+BMGC_DS05666,BMG_DS015052,,"Corneal Dystrophy, Juvenile Epithelial of Meesmann","Corneal Dystrophy, Juvenile Epithelial of Meesmann",,,,DOID:0060451,Meesmann corneal dystrophy,C0339277,D053559,,MONDO:0007379,Meesmann corneal dystrophy,
+BMGC_DS05667,BMG_DS015053,231930000,Reis-Bucklers' corneal dystrophy,,,,,DOID:0060453,Reis-Bucklers corneal dystrophy,C0339278,,608470,MONDO:0012043,Reis-Bucklers corneal dystrophy,Reis-Bucklers' corneal dystrophy | Reis-Bucklers' corneal dystrophy (disorder) | CDB type I corneal dystrophy
+BMGC_DS05668,BMG_DS015055,29504002,Polymorphous corneal dystrophy,,,,,,,C0339284,,,MONDO:0020364,posterior polymorphous corneal dystrophy,Polymorphous corneal dystrophy | Posterior polymorphous corneal dystrophy (disorder)
+BMGC_DS05669,BMG_DS015056,111523009,Acute hydrops keratoconus,,,,,DOID:10125,acute hydrops keratoconus,C0339286,,,MONDO:0000943,acute hydrops keratoconus,Acute hydrops keratoconus | Acute hydrops keratoconus (disorder) | Acute hydrops of the cornea
+BMGC_DS05670,BMG_DS015058,14366000,Exposure keratoconjunctivitis,,,,H16.21,DOID:9461,exposure keratitis,C0339295,,,MONDO:0004794,exposure keratitis,Exposure keratoconjunctivitis | Exposure keratoconjunctivitis (disorder) | Exposure keratitis | Exposure keratopathy | Lagophthalmic keratitis
+BMGC_DS05671,BMG_DS015059,128080005,Neurotrophic keratitis,,,,,,,C0339296,,MTHU010597,MONDO:0015290,neurotrophic keratopathy,Neurotrophic keratitis | Neurotrophic keratitis (disorder) | Anaesthetic keratopathy | Anesthetic keratopathy | Neurotrophic keratopathy | Neuroparalytic keratopathy
+BMGC_DS05672,BMG_DS015063,,,,,,,DOID:6199,cornea cancer,C0339304,,,MONDO:0021238,cornea neoplasm,
+BMGC_DS05673,BMG_DS015071,267619000,Non-infectious anterior uveitis,,,,,,,C0339317,,,MONDO:0017634,non-infectious anterior uveitis,Non-infectious anterior uveitis | Non-infectious anterior uveitis (disorder)
+BMGC_DS05674,BMG_DS015072,70461003,Lens-induced iridocyclitis,,9A96.Y,Other specified anterior uveitis,H20.2,DOID:9388,lens-induced iridocyclitis,C0339320,,,MONDO:0004775,lens-induced iridocyclitis,Lens-induced iridocyclitis | Lens-induced iridocyclitis (disorder)
+BMGC_DS05675,BMG_DS015077,,,,,,,DOID:4352,ciliary body cancer,C0339349,,,MONDO:0021229,ciliary body neoplasm,
+BMGC_DS05676,BMG_DS015092,56787009,Peripheral focal choroiditis AND chorioretinitis,,,,,DOID:11864,peripheral focal chorioretinitis,C0339394,,,MONDO:0001393,peripheral focal chorioretinitis,Peripheral focal choroiditis AND chorioretinitis | Peripheral focal choroiditis AND chorioretinitis (disorder) | Peripheral focal chorioretinitis
+BMGC_DS05677,BMG_DS015112,193468002,Partial central choroid dystrophy,,,,,DOID:9822,partial central choroid dystrophy,C0339427,,,MONDO:0004890,partial central choroid dystrophy,Partial central choroid dystrophy | Partial central choroid dystrophy (disorder) | Circinate choroidal dystrophy | Partial central dystrophy of choroid
+BMGC_DS05678,BMG_DS015117,,,,,,,DOID:2007,degeneration of macula and posterior pole,C0339436,,,MONDO:0002175,degeneration of macula and posterior pole,
+BMGC_DS05679,BMG_DS015118,193418005;267715002;193348007;155115009,Other retinal disorders,,,,H35,,,C0339438,,,,,Other retinal disorders &/or retinal haemorrhage | Haemorrhage - retinal | Hemorrhage - retinal | Other retinal disorders &/or retinal hemorrhage | Other retinal disorders | Other retinal disorders &/or retinal haemorrhage (disorder) | Other retinal disorders | Retinopathies | Other retinal disorders &/or retinopathies | Other retinal disorders &/or retinopathies (disorder) | Other retinal disorders | Other retinal disorders (disorder)
+BMGC_DS05680,BMG_DS015147,,,,,,,,,C0339498,,,MONDO:0041093,central retinal vein occlusion with macular edema,
+BMGC_DS05681,BMG_DS015152,,Vitelliform Macular Dystrophy,Vitelliform Macular Dystrophy,,,,DOID:0050661,vitelliform macular dystrophy,C0339510,D057826,,MONDO:0000390,vitelliform macular dystrophy,
+BMGC_DS05682,BMG_DS015154,,Leber Congenital Amaurosis,Leber Congenital Amaurosis,,,,DOID:14791,Leber congenital amaurosis,C0339527,D057130,,MONDO:0018998,Leber congenital amaurosis,
+BMGC_DS05683,BMG_DS015157,232058008,Usher syndrome type 2,,,,,,,C0339534,,,MONDO:0016484,Usher syndrome type 2,Usher syndrome type 2 | Usher syndrome type 2 (disorder)
+BMGC_DS05684,BMG_DS015158,,,,,,,,,C0339535,,,MONDO:0016293,congenital stationary night blindness,
+BMGC_DS05685,BMG_DS015159,,,,,,,,,C0339537,,303700,MONDO:0010563,blue cone monochromacy,
+BMGC_DS05686,BMG_DS015160,,Familial Exudative Vitreoretinopathies,Familial Exudative Vitreoretinopathies,,,,,,C0339539,D000080345,,MONDO:0019516,exudative vitreoretinopathy,
+BMGC_DS05687,BMG_DS015161,232065000,Goldmann-Favre syndrome (disorder),,,,,,,C0339541,,,MONDO:0100289,Goldmann-Favre syndrome,Goldmann-Favre syndrome | Goldmann-Favre syndrome (disorder) | Enhanced S-cone syndrome | Retinoschisis with early nyctalopia
+BMGC_DS05688,BMG_DS015163,,,,,,,DOID:2006,preretinal fibrosis,C0339543,,,MONDO:0002174,preretinal fibrosis,
+BMGC_DS05689,BMG_DS015164,,Retinal Pigment Epithelial Detachment,Retinal Detachment,,,,,,C0339546,D012163,,,,
+BMGC_DS05690,BMG_DS015168,,,,,,,DOID:774,retina lymphoma,C0339556,,,MONDO:0004349,retina lymphoma,
+BMGC_DS05691,BMG_DS015179,,,,,,,DOID:14548,steroid-induced glaucoma - borderline,C0339572,,,MONDO:0001996,steroid-induced glaucoma - borderline,
+BMGC_DS05692,BMG_DS015180,,"Glaucoma, Primary Open Angle","Glaucoma, Open-Angle",,,,DOID:1070,primary open angle glaucoma,C0339573,D005902,137760,MONDO:0100553,OPTN-related open angle glaucoma,
+BMGC_DS05693,BMG_DS015184,1654001,Corticosteroid-induced glaucoma,,,,,DOID:9946,steroid-induced glaucoma,C0339578,,,MONDO:0004930,steroid-induced glaucoma,Corticosteroid-induced glaucoma | Open angle glaucoma caused by corticosteroid (disorder) | Corticosteroid-induced open angle glaucoma | Open angle glaucoma caused by corticosteroid | Steroid responder open angle glaucoma
+BMGC_DS05694,BMG_DS015186,,,,,,,DOID:9948,residual stage corticosteroid-induced glaucoma,C0339580,,,MONDO:0004931,residual stage corticosteroid-induced glaucoma,
+BMGC_DS05695,BMG_DS015197,68241007,Glaucoma due to ocular trauma,,,,,DOID:13060,traumatic glaucoma,C0339594,,,MONDO:0001626,traumatic glaucoma,Traumatic glaucoma | Glaucoma due to ocular trauma | Glaucoma due to ocular trauma (disorder)
+BMGC_DS05696,BMG_DS015206,14785004,Monofixation syndrome,,,,H50.42,DOID:9843,monofixation syndrome,C0339611,,,MONDO:0004899,monofixation syndrome,Monofixation syndrome | Monofixation syndrome (disorder)
+BMGC_DS05697,BMG_DS015217,,Primary Esotropia,Esotropia,,,,,,C0339623,D004948,,,,
+BMGC_DS05698,BMG_DS015218,,Secondary Esotropia,Esotropia,,,,,,C0339624,D004948,,,,
+BMGC_DS05699,BMG_DS015262,,Corneal Astigmatism,Astigmatism,,,,,,C0339682,D001251,,,,
+BMGC_DS05700,BMG_DS015263,,Lenticular Astigmatism,Astigmatism,,,,,,C0339683,D001251,,,,
+BMGC_DS05701,BMG_DS015270,,Anisometropic Amblyopia,Amblyopia,,,,,,C0339696,D000550,,,,
+BMGC_DS05702,BMG_DS015274,,"Blindness, Acquired",Blindness,,,,,,C0339730,D001766,,,,
+BMGC_DS05703,BMG_DS015283,38394007,Chronic otitis media with perforation,,,,,,,C0339767,,,,,"Chronic purulent otitis media | Chronic suppurative otitis media | Chronic otitis media with effusion, purulent | CSOM - Chronic suppurative otitis media | Chronic secretory otitis media, purulent | Otitis media with effusion - purulent | Chronic otitis media with perforation | Chronic purulent otitis media (disorder)"
+BMGC_DS05704,BMG_DS015289,95828007,Congenital deafness,,,,,,,C0339789,,MTHU078470,,,Congenital deafness | Congenital deafness (disorder)
+BMGC_DS05705,BMG_DS015312,232340005,Disorder of nasal cavity,,,,,DOID:2163,nasal cavity disease,C0339820,,,MONDO:0002232,nasal cavity disorder,Disorder of nasal cavity | Disorder of nasal cavity (disorder)
+BMGC_DS05706,BMG_DS015331,,,,,,,,,C0339851,,161480,MONDO:0008064,"nasal bones, absence of",
+BMGC_DS05707,BMG_DS015357,196133001,Lung disease with systemic sclerosis,,,,,DOID:1578,pulmonary systemic sclerosis,C0339904,,,MONDO:0002047,pulmonary systemic sclerosis,Lung disease with systemic sclerosis | Lung disease with systemic sclerosis (disorder) | Scleroderma lung disease | Scleroderma of lung
+BMGC_DS05708,BMG_DS015375,195722003,Acute Moraxella catarrhalis bronchitis,,,,,,,C0339932,,,,,Acute Neisseria catarrhalis bronchitis | Acute Moraxella catarrhalis bronchitis (disorder) | Acute Moraxella catarrhalis bronchitis
+BMGC_DS05709,BMG_DS015376,233598009,Acute bacterial bronchitis,,,,,,,C0339933,,,,,Acute bacterial bronchitis | Acute bacterial bronchitis (disorder)
+BMGC_DS05710,BMG_DS015383,45556008;186297007,Pulmonary tularemia,,1B94.Y,Other specified tularaemia,A21.2,DOID:2122,pneumonic tularemia,C0339946,,,MONDO:0002212,pneumonic tularemia,Pulmonary tularemia | Bronchopneumonic tularemia | Pulmonary tularaemia | Bronchopneumonic tularaemia | Pulmonary tularemia (disorder) | Pneumonia with tularaemia | Tularaemia pneumonia | Pneumonia with tularemia | Tularemia pneumonia | Pneumonic tularaemia | Pneumonic tularemia | Pulmonary tularaemia | Pulmonary tularemia | Pulmonary tularemia (disorder)
+BMGC_DS05711,BMG_DS015390,195897008;233609002,Chlamydial pneumonia,,CA40.00,Pneumonia due to Chlamydophila pneumoniae,J16.0,DOID:0040083,Chlamydia pneumonia,C0339959,,,MONDO:0025598,pneumonia caused by chlamydia,Chlamydial pneumonia | Chlamydial pneumonia (disorder) | Chlamydial pneumonia | Pneumonia caused by Chlamydiaceae (disorder) | Pneumonia caused by Chlamydiaceae
+BMGC_DS05712,BMG_DS015399,233619008,Neonatal pneumonia,,,,,,,C0339968,,,,,Neonatal pneumonia | Neonatal pneumonia (disorder)
+BMGC_DS05713,BMG_DS015411,233629001,Idiopathic bronchiectasis,,,,,,,C0339985,,,MONDO:0018956,idiopathic bronchiectasis,Idiopathic bronchiectasis | Idiopathic bronchiectasis (disorder)
+BMGC_DS05714,BMG_DS015432,,,,,,,,,C0340014,,603523,MONDO:0011331,congenital chylothorax,
+BMGC_DS05715,BMG_DS015448,,"Immotile cilia syndrome, due to defective radial spokes",,,,,,,C0340035,C536286,242670,MONDO:0009449,ciliary dyskinesia with defective radial spokes,
+BMGC_DS05716,BMG_DS015450,,Young Syndrome,,,,,,,C0340037,C536718,279000,MONDO:0010220,Young syndrome,
+BMGC_DS05717,BMG_DS015451,,Ciliary Discoordination Due To Random Ciliary Orientation,,,,,,,C0340038,C562757,215518,MONDO:0008984,ciliary discoordination due to random ciliary orientation,
+BMGC_DS05718,BMG_DS015455,195951007,Acute exacerbation of chronic obstructive pulmonary disease,,,,,,,C0340044,,,,,Acute exacerbation of chronic obstructive airways disease | Acute exacerbation of chronic obstructive pulmonary disease | Acute exacerbation of COPD (chronic obstructive pulmonary disease) | Acute exacerbation of chronic obstructive pulmonary disease (disorder)
+BMGC_DS05719,BMG_DS015469,195967001,Hyperreactive airway disease,,,,,,,C0340062,,,,,Airway hyperreactivity | Asthmatic | Bronchial asthma | Bronchial hyperreactivity | BHR - Bronchial hyperreactivity | Bronchial hyperresponsiveness | Bronchial hypersensitivity | Asthma | Asthma (disorder) | Hyperreactive airway disease
+BMGC_DS05720,BMG_DS015491,,Summer-Type Hypersensitivity Pneumonitis,Trichosporonosis,,,,DOID:0050290,trichosporonosis,C0340092,D060586,,,,
+BMGC_DS05721,BMG_DS015498,233707008,High altitude pulmonary edema,,,,,,,C0340100,,,MONDO:0031257,high altitude pulmonary edema,High altitude pulmonary oedema | Pulmonary edema of mountaineers | Pulmonary oedema of mountaineers | High altitude pulmonary edema | High altitude pulmonary edema (disorder)
+BMGC_DS05722,BMG_DS015517,233726000,Localized pulmonary fibrosis,,,,,DOID:5642,localized pulmonary fibrosis,C0340127,,,MONDO:0003564,localized pulmonary fibrosis,Localised pulmonary fibrosis | Localized pulmonary fibrosis | Localized pulmonary fibrosis (disorder)
+BMGC_DS05723,BMG_DS015555,50076003,Baritosis,,,,,DOID:10321,baritosis,C0340177,C537080,,MONDO:0001001,baritosis,Baritosis | Barium lung | Baryta miners' disease | Barium lung disease | Baritosis (disorder) | Barytosis | Barium pneumoconiosis
+BMGC_DS05724,BMG_DS015562,233759002,Mixed mineral dust pneumoconiosis,,,,,DOID:10319,mixed mineral dust pneumoconiosis,C0340184,,,MONDO:0001000,mixed mineral dust pneumoconiosis,Mixed mineral dust pneumoconiosis | Mixed dust fibrosis | Mixed mineral dust pneumoconiosis (disorder)
+BMGC_DS05725,BMG_DS015564,1259003,Schistosis,,,,,DOID:10330,slate pneumoconiosis,C0340186,,,MONDO:0001004,slate pneumoconiosis,Schistosis | Slate-workers' lung | Slate workers pneumoconiosis | Slate pneumoconiosis | Schistosis (disorder)
+BMGC_DS05726,BMG_DS015571,,Hypoxemic Respiratory Failure,Respiratory Insufficiency,,,,,,C0340194,D012131,,,,
+BMGC_DS05727,BMG_DS015619,266249003;195127003;266310003;155383002,Ventricular hypertrophy,,,,,,,C0340279,,MTHU005304,,,Ventricular hypertrophy | Ventricular hypertrophy (disorder) | Ventricular hypertrophy (& [left]) | Ventricular hypertrophy | Left ventricular hypertrophy | Ventricular hypertrophy (& [left]) (disorder) | (Cardiomegaly) or (ventricular hypertrophy (& left)) | Left ventricular hypertrophy | Ventricular hypertrophy | Cardiomegaly | (Cardiomegaly) or (ventricular hypertrophy (& left)) (disorder)
+BMGC_DS05728,BMG_DS015623,194838005;155312003;233819005,Stable angina,,,,I20.89,,,C0340288,,,,,Stable angina | Stable angina (disorder)
+BMGC_DS05729,BMG_DS015634,,Inferior Wall Myocardial Infarction,Inferior Wall Myocardial Infarction,,,,DOID:5850,inferior myocardial infarction,C0340305,D056989,,MONDO:0006803,inferior myocardial infarction,
+BMGC_DS05730,BMG_DS015641,,,,,,,DOID:5853,lateral myocardial infarction,C0340312,,,MONDO:0003677,lateral myocardial infarction,
+BMGC_DS05731,BMG_DS015648,,,,,,,DOID:5847,posterior myocardial infarction,C0340319,,,MONDO:0003672,posterior myocardial infarction,
+BMGC_DS05732,BMG_DS015649,194796000;233843008,Silent myocardial infarction,,,,,DOID:5854,silent myocardial infarction,C0340324,,,MONDO:0003678,silent myocardial infarction,Coronary thrombosis | Thrombosis - coronary | Silent myocardial infarction | MI - Acute myocardial infarction | Heart attack | Cardiac rupture after acute myocardial infarction | Acute myocardial infarction | Attack - heart | Cardiac rupture following myocardial infarction (MI) | MI - acute myocardial infarction | (Myocardial infarction (& [acute] or [silent] or [cardiac rupture following])) or (coronary thrombosis) | (Myocardial infarction (& [acute] or [silent] or [cardiac rupture following])) or (coronary thrombosis) (disorder) | Silent myocardial infarction | MI - Silent myocardial infarction | Silent myocardial infarction (disorder)
+BMGC_DS05733,BMG_DS015662,95890006,Q fever endocarditis,,,,,,,C0340354,,,,,Q fever endocarditis | Q fever endocarditis (disorder) | Cardiac Q fever | Endocarditis - Q fever
+BMGC_DS05734,BMG_DS015670,,,,,,,,,C0340364,,,MONDO:0008004,familial mitral valve prolapse,
+BMGC_DS05735,BMG_DS015678,250915007;204368006,Subaortic stenosis,,,,,DOID:5805,subvalvular aortic stenosis,C0340375,,MTHU017461,MONDO:0006987,subvalvular aortic stenosis,Subaortic stenosis | Subaortic stenosis (disorder) | Subaortic stenosis | Subvalvular stenosis | Subvalvar stenosis | Subaortic stenosis (disorder)
+BMGC_DS05736,BMG_DS015707,52029003,Familial dilated cardiomyopathy,,,,,,,C0340427,,,MONDO:0016333,familial dilated cardiomyopathy,Primary familial dilated cardiomyopathy | Primary familial dilated cardiomyopathy (disorder) | Familial dilated cardiomyopathy
+BMGC_DS05737,BMG_DS015709,,,,,,,,,C0340429,,,MONDO:0016340,familial restrictive cardiomyopathy,
+BMGC_DS05738,BMG_DS015730,,Premature Cardiac Complex,"Cardiac Complexes, Premature",,,,,,C0340464,D005117,,,,
+BMGC_DS05739,BMG_DS015744,,Familial Polymorphic Ventricular Tachycardia,Polymorphic Catecholaminergic Ventricular Tachycardia,,,,,,C0340485,D000098850,192605,MONDO:0008648,"ventricular tachycardia, familial",
+BMGC_DS05740,BMG_DS015750,233913007,Familial sick sinus syndrome,,,,,,,C0340491,,,MONDO:0012061,familial sick sinus syndrome,Familial sick sinus syndrome | Familial sick sinus syndrome (disorder)
+BMGC_DS05741,BMG_DS015751,233915000,Paroxysmal familial ventricular fibrillation,,,,,,,C0340493,C537182,,MONDO:0100234,paroxysmal familial ventricular fibrillation,Paroxysmal familial ventricular fibrillation | Paroxysmal familial ventricular fibrillation (disorder)
+BMGC_DS05742,BMG_DS015752,195062005,Other conduction disorders,,,,I45,,,C0340494,,,,,Other conduction disorders | Other conduction disorders (disorder)
+BMGC_DS05743,BMG_DS015755,,"Bundle Branch Block, Familial Isolated Complete Right",,,,,,,C0340504,C562759,113950,MONDO:0007241,"bundle branch block, familial isolated complete right",
+BMGC_DS05744,BMG_DS015773,233944003,Familial primary pulmonary hypertension,,,,,,,C0340543,,,MONDO:0017148,heritable pulmonary arterial hypertension,Familial primary pulmonary hypertension | Familial primary pulmonary hypertension (disorder)
+BMGC_DS05745,BMG_DS015774,233945002,Pulmonary arterial hypertension induced by drug,,,,,,,C0340544,,,MONDO:0017149,drug- or toxin-induced pulmonary arterial hypertension,Drug-induced pulmonary hypertension | Pulmonary arterial hypertension induced by drug | Pulmonary hypertension caused by drug (disorder) | Pulmonary arterial hypertension caused by drug | Pulmonary hypertension caused by drug
+BMGC_DS05746,BMG_DS015777,233949008,Pulmonary capillary hemangiomatosis,,,,,,,C0340548,,MTHU041934,,,Pulmonary capillary haemangiomatosis | Pulmonary capillary hemangiomatosis | Pulmonary capillary hemangiomatosis (disorder)
+BMGC_DS05747,BMG_DS015781,233954004,High altitude pulmonary hypertension,,,,,,,C0340552,C535833,178400,MONDO:0008344,"pulmonary edema of mountaineers, susceptibility to",High altitude pulmonary hypertension | Pulmonary hypertension caused by low air pressure due to chronic exposure to high altitude | Pulmonary hypertension caused by low air pressure due to chronic exposure to high altitude (disorder)
+BMGC_DS05748,BMG_DS015791,,Internal Carotid Artery Stenosis,Carotid Stenosis,,,,,,C0340569,D016893,,MONDO:0005189,internal carotid artery stenosis,
+BMGC_DS05749,BMG_DS015806,95579008,Thrombosis of renal artery,,,,,,,C0340608,,,,,Thrombosis of renal artery | Renal artery thrombosis | Thrombosis of renal artery (disorder)
+BMGC_DS05750,BMG_DS015813,,Anterior Spinal Artery Dissection,Anterior Spinal Artery Syndrome,,,,,,C0340642,D020759,,,,
+BMGC_DS05751,BMG_DS015814,308546005,Dissection of aorta,,BD50.Z,"Aortic aneurysm or dissection, unspecified",I71.0,,,C0340643,,,,,Dissection of aorta | Dissection of aorta (disorder)
+BMGC_DS05752,BMG_DS015898,,,,,,,,,C0340803,,,MONDO:0016231,capillary malformation,
+BMGC_DS05753,BMG_DS015899,191329002,Hereditary vascular fragility,,,,,,,C0340804,,,,,Capillary fragility - hereditary | Hereditary vascular fragility | Hereditary vascular fragility (disorder)
+BMGC_DS05754,BMG_DS015900,,,,,,,,,C0340826,,271500,MONDO:0010067,splenoportal vascular anomalies,
+BMGC_DS05755,BMG_DS015901,234146006,Hennekam lymphangiectasia-lymphedema syndrome,,,,,DOID:0060366,Hennekam syndrome,C0340834,,,MONDO:0016256,Hennekam syndrome,"Hennekam lymphangiectasia-lymphoedema syndrome | Hennekam lymphangiectasia-lymphedema syndrome | Hennekam lymphangiectasia-lymphedema syndrome (disorder) | Hennekam syndrome | Lymphoedema, lymphangiectasia, intellectual disability syndrome | Lymphedema, lymphangiectasia, intellectual disability syndrome"
+BMGC_DS05756,BMG_DS015903,,"PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE",,,,,DOID:0081269,pulmonary venoocclusive disease 2,C0340848,,234810,MONDO:0009329,pulmonary venoocclusive disease 2,
+BMGC_DS05757,BMG_DS015907,,"Syncope, Situational",Syncope,,,,,,C0340854,D013575,,,,
+BMGC_DS05758,BMG_DS015908,,"Syncope, Micturition",Syncope,,,,,,C0340855,D013575,,,,
+BMGC_DS05759,BMG_DS015981,124331002,Deficiency of pyruvate kinase,,,,,,,C0340968,,266200,MONDO:0009950,pyruvate kinase deficiency of red cells,Deficiency of phosphoenolpyruvate kinase | Deficiency of phosphoenol transphosphorylase | Deficiency of pyruvate kinase | Deficiency of pyruvate kinase (disorder) | PK - Pyruvate kinase deficiency | Pyruvate kinase deficiency
+BMGC_DS05760,BMG_DS015997,196305005,Odontoclasia,,,,,DOID:11736,odontoclasia,C0341004,,,MONDO:0001349,odontoclasia,Odontoclasia | Odontoclasia (disorder)
+BMGC_DS05761,BMG_DS016006,110267003,Streptococcal infection of mouth,,,,,,,C0341016,,,,,Streptococcal infection of mouth | Streptococcal stomatitis | Streptococcal infection of mouth (disorder)
+BMGC_DS05762,BMG_DS016013,235073000,Familial chronic mucocutaneous candidiasis,,,,,,,C0341024,C537979,613108,MONDO:0013140,"candidiasis, familial, 4",Familial chronic mucocutaneous candidiasis | FCMC - Familial chronic mucocutaneous candidosis | FCMC - Familial chronic mucocutaneous candidiasis | Familial chronic mucocutaneous candidosis | Familial chronic mucocutaneous candidiasis (disorder)
+BMGC_DS05763,BMG_DS016038,235599003,Eosinophilic esophagitis,,,,K20.0,DOID:13922,eosinophilic esophagitis,C0341106,,MTHU054726,MONDO:0005361,eosinophilic esophagitis,Eosinophilic esophagitis | Eosinophilic oesophagitis | Eosinophilic esophagitis (disorder)
+BMGC_DS05764,BMG_DS016040,235601001,Bacterial esophagitis,,,,,DOID:13921,bacterial esophagitis,C0341108,,,MONDO:0001832,bacterial esophagitis,Bacterial esophagitis | Bacterial oesophagitis | Bacterial esophagitis (disorder)
+BMGC_DS05765,BMG_DS016041,235602008,Fungal esophagitis,,,,,DOID:13147,fungal esophagitis,C0341109,,,MONDO:0001649,fungal esophagitis,Fungal oesophagitis | Fungal esophagitis | Fungal esophagitis (disorder)
+BMGC_DS05766,BMG_DS016042,235603003,Viral esophagitis,,,,,DOID:6297,viral esophagitis,C0341110,,,MONDO:0003846,viral esophagitis,Viral esophagitis | Viral oesophagitis | Viral esophagitis (disorder)
+BMGC_DS05767,BMG_DS016065,,"Esophageal Ring, Lower",,,,,,,C0341137,C562765,133240,MONDO:0007577,"esophageal ring, lower",
+BMGC_DS05768,BMG_DS016182,,Microvillus inclusion disease,,,,,DOID:0060775,microvillus inclusion disease,C0341306,C537470,251850,MONDO:0009635,microvillus inclusion disease,
+BMGC_DS05769,BMG_DS016197,235746007,Indeterminate colitis,,DD72,Indeterminate colitis,K52.3,,,C0341332,,,MONDO:0006038,indeterminate colitis,Indeterminate colitis | Indeterminate colitis (disorder)
+BMGC_DS05770,BMG_DS016200,,Cytomegalovirus Colitis,Cytomegalovirus Infections,,,,,,C0341335,D003586,,,,
+BMGC_DS05771,BMG_DS016274,,,,,,,DOID:3918,pancreatic cystadenoma,C0341486,,,MONDO:0002809,pancreatic cystadenoma,
+BMGC_DS05772,BMG_DS016284,197171003,Bacterial peritonitis,,,,,,,C0341503,,,MONDO:0005195,septic peritonitis,Bacterial peritonitis | Bacterial peritonitis (disorder)
+BMGC_DS05773,BMG_DS016299,111839008,Intestinal infection caused by Escherichia coli,,,,,,,C0341558,,,,,Escherichia gastroenteritis | Enteric colibacillosis | Escherichia coli gastrointestinal tract infection | Intestinal infection caused by E. coli | Intestinal infection caused by Escherichia coli (disorder) | Intestinal infection caused by Escherichia coli
+BMGC_DS05774,BMG_DS016339,,,,,,,,,C0341677,,,MONDO:0001343,impaired renal function disease,
+BMGC_DS05775,BMG_DS016347,197585004,Acute diffuse nephritis,,,,,DOID:14066,acute diffuse nephritis,C0341689,,,MONDO:0001871,acute diffuse glomerulonephritis,Acute diffuse nephritis | Acute diffuse nephritis (disorder)
+BMGC_DS05776,BMG_DS016350,197579006,Acute proliferative glomerulonephritis,,,,,DOID:13138,acute proliferative glomerulonephritis,C0341692,,,MONDO:0001644,acute proliferative glomerulonephritis,PGN - Acute proliferative glomerulonephritis | Acute proliferative glomerulonephritis | Acute proliferative glomerulonephritis (disorder)
+BMGC_DS05777,BMG_DS016352,,,,,,,DOID:11036,chronic rapidly progressive glomerulonephritis,C0341694,,,MONDO:0001184,chronic rapidly progressive glomerulonephritis,
+BMGC_DS05778,BMG_DS016353,197676009;197659005,Atrophy of kidney,,,,,,,C0341698,,,,,Atrophy of kidney | Atrophy of kidney (disorder) | Atrophy of kidney | Renal atrophy | Atrophy of kidney (disorder)
+BMGC_DS05779,BMG_DS016356,236468006,Adult Fanconi syndrome,,,,,DOID:1062,Fanconi syndrome,C0341703,,,MONDO:0060778,adult Fanconi syndrome,Adult Fanconi syndrome | Adult Fanconi syndrome (disorder)
+BMGC_DS05780,BMG_DS016370,236655005,Detrusor and sphincter dyssynergia,,,,,DOID:12145,detrusor sphincter dyssynergia,C0341747,,,MONDO:0001447,detrusor sphincter dyssynergia,Detrusor and sphincter dyssynergia | DSD - Detrusor and sphincter dyssynergia | Detrusor and sphincter dyssynergia (disorder)
+BMGC_DS05781,BMG_DS016378,,,,,,,DOID:2139,paraurethral gland neoplasm,C0341766,,,MONDO:0002219,paraurethral gland neoplasm,
+BMGC_DS05782,BMG_DS016379,,,,,,,DOID:3855,seminal vesicle tumor,C0341767,,,MONDO:0002790,seminal vesicle tumor,
+BMGC_DS05783,BMG_DS016386,197997008;236767000,Chlamydial epididymitis,,,,A56.19,,,C0341779,,,,,Chlamydial epididymitis | Chlamydial epididymitis (disorder)
+BMGC_DS05784,BMG_DS016390,,,,,,,DOID:518,scrotum neoplasm,C0341790,,,MONDO:0003319,scrotum neoplasm,
+BMGC_DS05785,BMG_DS016406,,,,,,,DOID:2152,ovary epithelial cancer,C0341823,,,MONDO:0002229,ovarian epithelial tumor,
+BMGC_DS05786,BMG_DS016421,76376003,Endometriosis of uterus,,GA11,Adenomyosis,N80.0,DOID:288,endometriosis of uterus,C0341858,,,,,Endometriosis of uterus | Endometriosis of uterus (disorder)
+BMGC_DS05787,BMG_DS016427,,"Subfertility, Female","Infertility, Female",,,,,,C0341869,D007247,,,,
+BMGC_DS05788,BMG_DS016464,,,,,,,,,C0341950,,,MONDO:0001641,severe pre-eclampsia,
+BMGC_DS05789,BMG_DS016537,57777000,Toxic nodular goiter,,,,,DOID:11277,Plummer's disease,C0342127,,,MONDO:0001252,Plummer disease,Toxic nodular goiter | Toxic adenomatous goiter | Toxic struma nodosa | Plummer's disease | Toxic nodular goitre | Toxic adenomatous goitre | Toxic nodular goiter (disorder)
+BMGC_DS05790,BMG_DS016556,190272004;237515009,Congenital hypothyroidism without goiter,,5A00.01,Permanent congenital hypothyroidism without goitre,E03.1,DOID:0070124;DOID:0111140;DOID:0070126;DOID:0070128;DOID:0070125;DOID:0070123;DOID:0070127,congenital nongoitrous hypothyroidism 2 | congenital nongoitrous hypothyroidism 5 | congenital nongoitrous hypothyroidism 1 | congenital nongoitrous hypothyroidism 3 | congenital nongoitrous hypothyroidism 6 | congenital nongoitrous hypothyroidism 4 | IGSF1 deficiency syndrome,C0342151,,,,,Congenital hypothyroidism without goiter | Congenital hypothyroidism without goitre | Congenital hypothyroidism without goitre (disorder) | Congenital hypothyroidism without goitre | Congenital hypothyroidism without goiter | Congenital hypothyroidism without goiter (disorder)
+BMGC_DS05791,BMG_DS016559,,"Hypothyroidism, Autoimmune",,,,,,,C0342158,C562768,,,,
+BMGC_DS05792,BMG_DS016577,,"Hyperthyroxinemia, Familial Dysalbuminemic","Hyperthyroxinemia, Familial Dysalbuminemic",,,,,,C0342185,D050010,615999,MONDO:0014448,"hyperthyroxinemia, familial dysalbuminemic",
+BMGC_DS05793,BMG_DS016580,237552009,C-cell hyperplasia of thyroid,,5A04,Hypersecretion of calcitonin,E07.0,,,C0342190,,,MONDO:0006120,C-cell hyperplasia,C-cell hyperplasia of thyroid | C-cell hyperplasia of thyroid (disorder)
+BMGC_DS05794,BMG_DS016584,,Thyroid Dyshormonogenesis 3,,,,,DOID:0112187,thyroid dyshormonogenesis 3,C0342194,C562769,274700,MONDO:0010135,thyroid dyshormonogenesis 3,
+BMGC_DS05795,BMG_DS016585,,Thyroid Dyshormonogenesis 4,,,,,DOID:0112188,thyroid dyshormonogenesis 4,C0342195,C562770,274800,MONDO:0010136,thyroid dyshormonogenesis 4,
+BMGC_DS05796,BMG_DS016586,,Thyroid Dyshormonogenesis 5,,,,,DOID:0112184,thyroid dyshormonogenesis 5,C0342196,C562771,274900,MONDO:0010137,thyroid dyshormonogenesis 5,
+BMGC_DS05797,BMG_DS016588,237562002,Iodine deficiency syndrome,,,,,,,C0342199,,,,,Iodine deficiency syndrome | Iodine deficiency syndrome (disorder)
+BMGC_DS05798,BMG_DS016589,,Endemic Cretinism,Congenital Hypothyroidism,,,,DOID:0050328,congenital hypothyroidism,C0342200,D003409,,,,
+BMGC_DS05799,BMG_DS016610,,Complications of Diabetes Mellitus,Diabetes Complications,,,,,,C0342257,D048909,,,,
+BMGC_DS05800,BMG_DS016620,237603002,Transitory neonatal diabetes mellitus,,,,,,,C0342273,,,MONDO:0020525,transient neonatal diabetes mellitus,Transitory neonatal diabetes mellitus | Transitory neonatal diabetes mellitus (disorder) | Transient neonatal diabetes mellitus
+BMGC_DS05801,BMG_DS016622,28453007;400971001,Maturity onset diabetes mellitus in young,,,,,,,C0342276,,606391,MONDO:0018911,maturity-onset diabetes of the young,Maturity onset diabetes mellitus in young | MODY | Autosomal dominant diabetes mellitus | NIDDY | Diabetes mellitus autosomal dominant | MODY - Maturity onset diabetes in youth type 1 | MODY - Maturity onset diabetes in youth type I | Mason-type diabetes | Maturity onset diabetes in youth | Maturity onset diabetes mellitus in young (disorder) | Maturity onset diabetes in youth type 1 | Maturity onset diabetes mellitus in young (disorder) | Maturity onset diabetes mellitus in young
+BMGC_DS05802,BMG_DS016623,237604008,Diabetes mellitus autosomal dominant type II (disorder),,,,,,,C0342277,,125851,MONDO:0007453,maturity-onset diabetes of the young type 2,"Diabetes mellitus autosomal dominant type II | Maturity onset diabetes in youth type II | Maturity onset diabetes in youth type 2 | Maturity onset diabetes of the young, type 2 (disorder) | Maturity onset diabetes of the young, type 2 | GCK (glucokinase) monogenic diabetes mellitus | MODY2 (maturity onset diabetes of the young type 2)"
+BMGC_DS05803,BMG_DS016624,237606005,Hereditary benign acanthosis nigricans with insulin resistance,,,,,,,C0342278,,610549,MONDO:0012520,insulin-resistance syndrome type A,Hereditary benign acanthosis nigricans with insulin resistance | Insulin-resistant acanthosis nigricans type A | Insulin receptor defect with insulin-resistant diabetes mellitus and acanthosis nigricans | Hereditary benign acanthosis nigricans with insulin resistance (disorder)
+BMGC_DS05804,BMG_DS016625,,AREDYLD Syndrome,,,,,,,C0342280,C537427,207780,MONDO:0008812,AREDYLD syndrome,
+BMGC_DS05805,BMG_DS016626,,"Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus",,,,,,,C0342281,C562774,158500,MONDO:0008023,muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome,
+BMGC_DS05806,BMG_DS016627,,Multiple synostoses syndrome 1,,,,,,,C0342282,C536943,186500,MONDO:0008519,multiple synostoses syndrome 1,
+BMGC_DS05807,BMG_DS016628,237613005,Hyperproinsulinemia,,,,,,,C0342283,C562776,MTHU069939;616214,MONDO:0014535,hyperproinsulinemia,Hyperproinsulinaemia | Hyperproinsulinemia | Hyperproinsulinemia (disorder)
+BMGC_DS05808,BMG_DS016629,237614004,Bangstad syndrome,,,,,,,C0342284,C537902,210740,MONDO:0008874,Bangstad syndrome,"Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency | Bangstad syndrome | Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goitre, and primary gonadal insufficiency | Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency (disorder)"
+BMGC_DS05809,BMG_DS016630,816067005,Woodhouse Sakati syndrome,,,,,DOID:0112264,Woodhouse-Sakati syndrome,C0342286,C536742,241080,MONDO:0009419,Woodhouse-Sakati syndrome,"Diabetes, hypogonadism, deafness, intellectual disability syndrome | Woodhouse Sakati syndrome | Diabetes, hypogonadism, deafness, intellectual disability syndrome (disorder)"
+BMGC_DS05810,BMG_DS016631,,,,,,,DOID:0090117,thiamine-responsive megaloblastic anemia syndrome,C0342287,,249270,MONDO:0009575,thiamine-responsive megaloblastic anemia syndrome,
+BMGC_DS05811,BMG_DS016632,237618001,Insulin-dependent diabetes mellitus secretory diarrhea syndrome,,,,,,,C0342288,,304790,MONDO:0010580,immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome,Insulin-dependent diabetes mellitus secretory diarrhoea syndrome | Congenital insulin-dependent diabetes mellitus with fatal secretory diarrhea | Congenital insulin-dependent diabetes mellitus with fatal secretory diarrhoea | Insulin-dependent diabetes mellitus secretory diarrhea syndrome | Insulin-dependent diabetes mellitus secretory diarrhea syndrome (disorder)
+BMGC_DS05812,BMG_DS016633,237619009,Diabetes-deafness syndrome maternally transmitted,,,,,,,C0342289,,520000,MONDO:0010785,maternally-inherited diabetes and deafness,Ballinger-Wallace syndrome | Diabetes-deafness syndrome maternally transmitted | Maternally inherited diabetes and deafness (disorder) | Maternally inherited diabetes and deafness | MIDD - maternally inherited diabetes and deafness | Maternally-inherited diabetes and hearing loss | Mitochondrial diabetes
+BMGC_DS05813,BMG_DS016650,237633009,Hypoglycemia due to diabetes mellitus,,,,,,,C0342313,,,,,Hypoglycemic state in diabetes | Hypoglycaemic state in diabetes | Hypoglycemic state due to diabetes mellitus | Hypoglycaemic state due to diabetes mellitus | Hypoglycaemia due to diabetes mellitus | Hypoglycemia due to diabetes mellitus | Hypoglycemia due to diabetes mellitus (disorder)
+BMGC_DS05814,BMG_DS016663,237651005,Insulin resistance - type A,,,,,,,C0342336,,,,,Insulin resistance - type A | Insulin resistance - type A (disorder) | Type A insulin resistance
+BMGC_DS05815,BMG_DS016668,,Idiopathic Hypoparathyroidism,Hypoparathyroidism,,,,,,C0342342,D007011,,,,
+BMGC_DS05816,BMG_DS016669,237655001,Hypoparathyroidism - X-linked,,,,,,,C0342344,,307700,MONDO:0010618,familial isolated hypoparathyroidism due to agenesis of parathyroid gland,Hypoparathyroidism - X-linked | X-linked hypoparathyroidism (disorder) | X-linked hypoparathyroidism
+BMGC_DS05817,BMG_DS016670,237657009,Hypoparathyroidism - autosomal dominant,,,,,,,C0342345,,601198,MONDO:0011013,autosomal dominant hypocalcemia 1,Hypoparathyroidism - autosomal dominant | Hypoparathyroidism - autosomal dominant (disorder)
+BMGC_DS05818,BMG_DS016680,237683004,Panhypopituitarism - X-linked,,,,,,,C0342376,,312000,MONDO:0010712,"panhypopituitarism, X-linked",Panhypopituitarism - X-linked | X-linked panhypopituitarism (disorder) | X-linked panhypopituitarism
+BMGC_DS05819,BMG_DS016683,237688008,Idiopathic growth hormone deficiency,,5A61.0,Hypopituitarism,E23.0,DOID:0090072;DOID:0090087;DOID:0060875;DOID:0090073;DOID:0090076;DOID:0090092;DOID:0060873;DOID:0090080;DOID:0090075;DOID:0090077;DOID:0090071;DOID:0090082;DOID:0090084;DOID:0090074;DOID:0090093;DOID:0060874;DOID:0090078;DOID:0090070;DOID:0090085;DOID:0090094;DOID:0090086;DOID:0090083;DOID:0090081;DOID:0090079;DOID:0090089;DOID:0090090,hypogonadotropic hypogonadism 5 with or without anosmia | hypogonadotropic hypogonadism 7 with or without anosmia | hypogonadotropic hypogonadism 9 with or without anosmia | isolated growth hormone deficiency type IB | hypogonadotropic hypogonadism 21 with or without anosmia | hypogonadotropic hypogonadism 17 with or without anosmia | hypogonadotropic hypogonadism 6 with or without anosmia | isolated growth hormone deficiency type IA | isolated growth hormone deficiency type III | hypogonadotropic hypogonadism 10 with or without anosmia | hypogonadotropic hypogonadism 2 with or without anosmia | hypogonadotropic hypogonadism 22 with or without anosmia | hypogonadotropic hypogonadism 4 with or without anosmia | hypogonadotropic hypogonadism 1 with or without anosmia | hypogonadotropic hypogonadism 15 with or without anosmia | hypogonadotropic hypogonadism 16 with or without anosmia | hypogonadotropic hypogonadism 3 with or without anosmia | hypogonadotropic hypogonadism 14 with or without anosmia | hypogonadotropic hypogonadism 13 with or without anosmia | hypogonadotropic hypogonadism 19 with or without anosmia | hypogonadotropic hypogonadism 18 with or without anosmia | hypogonadotropic hypogonadism 12 with or without anosmia | hypogonadotropic hypogonadism | hypogonadotropic hypogonadism 11 with or without anosmia | hypogonadotropic hypogonadism 8 with or without anosmia | hypogonadotropic hypogonadism 20 with or without anosmia,C0342381,,,,,Idiopathic growth hormone insufficiency | IGHD - Idiopathic growth hormone deficiency | Idiopathic growth hormone deficiency | Idiopathic growth hormone deficiency (disorder)
+BMGC_DS05820,BMG_DS016685,123953004,Idiopathic hypogonadotropic hypogonadism,,,,,,,C0342384,,146110,MONDO:0007794,hypogonadotropic hypogonadism 7 with or without anosmia,Idiopathic hypogonadotropic hypogonadism | Idiopathic gonadotrophin deficiency | Idiopathic hypogonadotropic hypogonadism (disorder)
+BMGC_DS05821,BMG_DS016688,237692001,Adrenocorticotropic hormone (ACTH) deficiency (disorder),,,,,,,C0342388,,201400,MONDO:0008720,congenital isolated adrenocorticotropic hormone deficiency,Secondary hypoadrenalism | ACTH deficiency | Adrenocorticotropic hormone (ACTH) deficiency | Adrenocorticotropic hormone deficiency (disorder) | Adrenocorticotropic hormone deficiency
+BMGC_DS05822,BMG_DS016689,237696003,Familial vasopressin deficiency,,,,,,,C0342394,,125700,MONDO:0007450,neurohypophyseal diabetes insipidus,Familial central diabetes insipidus | Familial vasopressin deficiency | Familial arginine vasopressin deficiency (disorder) | Familial AVP-D (arginine vasopressin deficiency) | Familial arginine vasopressin deficiency
+BMGC_DS05823,BMG_DS016698,95830009,Pituitary infarction,,,,,DOID:1130,pituitary infarct,C0342405,,,MONDO:0001259,pituitary gland infarction,Pituitary infarction | Pituitary infarct | Pituitary infarction (disorder)
+BMGC_DS05824,BMG_DS016707,,,,,,,,,C0342418,,241800,MONDO:0009436,congenital hypothalamic hamartoma syndrome,
+BMGC_DS05825,BMG_DS016734,54470008,3 beta-Hydroxysteroid dehydrogenase deficiency,,,,,,,C0342471,,201810,MONDO:0008727,congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency,"3 beta-Hydroxysteroid dehydrogenase deficiency | 3 beta-HSD deficiency | Congenital adrenal hyperplasia, type 4 | CAH - 3 beta-dehydrogenase deficiency | 3 beta-Hydroxysteroid dehydrogenase deficiency (disorder)"
+BMGC_DS05826,BMG_DS016735,49013001,17 alpha-Hydroxyprogesterone aldolase deficiency,,,,,,,C0342473,,,,,"17 alpha-Hydroxyprogesterone aldolase deficiency | Steroid 17,20-lyase deficiency | Male pseudohermaphroditism due to testicular 17,20-desmolase deficiency | Defective synthesis of 17-20 desmolase | 17 alpha-Hydroxyprogesterone aldolase deficiency (disorder)"
+BMGC_DS05827,BMG_DS016736,,Lipoid congenital adrenal hyperplasia,,,,,,,C0342474,C537027,201710,MONDO:0008725,congenital lipoid adrenal hyperplasia due to STAR deficency,
+BMGC_DS05828,BMG_DS016740,,X-linked Adrenal Hypoplasia,"Hypoadrenocorticism, Familial",,,,,,C0342482,D000075262,300200,MONDO:0010264,X-linked adrenal hypoplasia congenita,
+BMGC_DS05829,BMG_DS016743,,"Mineralocorticoid Excess Syndrome, Apparent","Mineralocorticoid Excess Syndrome, Apparent",,,,DOID:4367,apparent mineralocorticoid excess syndrome,C0342488,D043204,218030,MONDO:0009025,apparent mineralocorticoid excess,
+BMGC_DS05830,BMG_DS016747,237778003,Macronodular adrenal hyperplasia,,,,,,,C0342495,,MTHU020776,,,Macronodular adrenal hyperplasia | Macronodular adrenal hyperplasia (disorder)
+BMGC_DS05831,BMG_DS016766,38825009,Deficiency of testosterone biosynthesis,,,,,,,C0342527,,,,,Deficiency of testosterone biosynthesis | Androgen deficiency | Defective biosynthesis of testicular androgen | Defect of testicular androgen synthesis | Deficiency of testosterone biosynthesis (disorder)
+BMGC_DS05832,BMG_DS016777,,Central Precocious Puberty,"Puberty, Precocious",,,,DOID:0112308,central precocious puberty,C0342543,D011629,,MONDO:0019165,central precocious puberty,
+BMGC_DS05833,BMG_DS016781,,Familial Testotoxicosis,,,,,DOID:0111545,familial male-limited precocious puberty,C0342549,C536961,176410,MONDO:0008303,familial male-limited precocious puberty,
+BMGC_DS05834,BMG_DS016788,237833006,Carcinoid crisis,,,,,,,C0342569,,,MONDO:0041167,carcinoid crisis,Carcinoid crisis | Carcinoid crisis (disorder)
+BMGC_DS05835,BMG_DS016790,,,,,,,,,C0342573,,262400,MONDO:0009876,isolated growth hormone deficiency type IA,
+BMGC_DS05836,BMG_DS016799,,"Amyloid Polyneuropathy, British Type","Amyloid Neuropathies, Familial",,,,,,C0342608,D028227,,,,
+BMGC_DS05837,BMG_DS016801,237868006,Familial non-neuropathic amyloidosis,,,,,,,C0342611,,,,,Familial non-neuropathic amyloidosis | Familial non-neuropathic amyloidosis (disorder) | Nonneuropathic heredofamilial amyloidosis
+BMGC_DS05838,BMG_DS016812,157145008;206482007;268846006,Neonatal hypocalcemia,,,,,,,C0342634,,MTHU015276,,,Neonatal hypocalcaemia | Neonatal hypocalcemia | Neonatal hypocalcaemia (disorder) | Cow's milk hypocalcaemia | Neonatal hypocalcaemia | (Hypocalcaemia: [neonatal] or [cow's milk]) or (neonatal hypoparathroidism) | Cow's milk hypocalcemia | Neonatal hypocalcemia | Neonatal hypoparathroidism | (Hypocalcemia: [neonatal] or [cow's milk]) or (neonatal hypoparathroidism) | (Hypocalcaemia: [neonatal] or [cow's milk]) or (neonatal hypoparathroidism) (disorder) | Neonatal hypocalcaemia | Neonatal hypocalcemia | Neonatal hypocalcemia (disorder)
+BMGC_DS05839,BMG_DS016815,,"Hypocalciuric hypercalcemia, familial, type 1",,,,,,,C0342637,C537145,145980,MONDO:0007791,familial hypocalciuric hypercalcemia 1,
+BMGC_DS05840,BMG_DS016817,,,,,,,,,C0342639,,143870,MONDO:0007748,"hypercalciuria, absorptive, 2",
+BMGC_DS05841,BMG_DS016819,237889002,Autosomal dominant hypophosphatemic rickets,,,,,,,C0342642,,193100,MONDO:0008660,autosomal dominant hypophosphatemic rickets,Autosomal dominant hypophosphatemic rickets | Autosomal dominant hypophosphataemic rickets | Autosomal dominant hypophosphatemic rickets (disorder)
+BMGC_DS05842,BMG_DS016820,90505000,Autosomal recessive hypophosphatemic vitamin D refractory rickets,,,,,,,C0342643,,,MONDO:0017324,autosomal recessive hypophosphatemic rickets,Autosomal recessive hypophosphatemic vitamin D refractory rickets | Autosomal recessive hypophosphataemic vitamin D refractory rickets | Autosomal recessive hypophosphatemic vitamin D refractory rickets (disorder) | Autosomal recessive hypophosphataemic rickets | Autosomal recessive hypophosphatemic rickets
+BMGC_DS05843,BMG_DS016821,,"Vitamin D-Dependent Rickets, Type 2A",,,,,,,C0342646,C562794,277440,MONDO:0010186,"vitamin D-dependent rickets, type 2A",
+BMGC_DS05844,BMG_DS016823,237897009;129759000,Vascular calcification,,,,,,,C0342649,,,,,"Vascular calcification | Vascular calcification (disorder) | Vascular calcification, radiographic finding | Radiographic finding of vascular calcification (finding) | Radiographic finding of vascular calcification"
+BMGC_DS05845,BMG_DS016838,,"ALBINISM, OCULOCUTANEOUS, TYPE III",,,,,DOID:0070097,oculocutaneous albinism type III,C0342683,,115501;278400;203290;203290,MONDO:0008747,oculocutaneous albinism type 3,
+BMGC_DS05846,BMG_DS016839,78642008,"Ocular albinism, type I",,,,,,,C0342684,,300500,MONDO:0021019,X-linked recessive ocular albinism,"X-linked ocular albinism, Nettleship type | Nettleship-Falls type ocular albinism | Ocular albinism, type I | Ocular albinism, type I (disorder) | OA1 - X-linked ocular albinism | X-linked ocular albinism | X-linked recessive ocular albinism | X linked ocular albinism"
+BMGC_DS05847,BMG_DS016842,,dopamine beta hydroxylase deficiency,,,,,DOID:0090145,dopamine beta-hydroxylase deficiency,C0342687,C535600,,,,
+BMGC_DS05848,BMG_DS016849,,Transcobalamin I Deficiency,,,,,,,C0342700,C562798,193090,MONDO:0008659,transcobalamin I deficiency,
+BMGC_DS05849,BMG_DS016850,191143002;237934001,Transcobalamin II deficiency,,3A01.0,Hereditary vitamin B12 deficiency anaemia,D51.2,,,C0342701,,MTHU008999;275350,MONDO:0010149,transcobalamin II deficiency,Transcobalamin II deficiency | Transcobalamin II deficiency (disorder) | TCN2 - Transcobalamin II deficiency | Transcobalamin II deficiency | Transcobalamin II deficiency (disorder)
+BMGC_DS05850,BMG_DS016854,,"Folate Malabsorption, Hereditary",,,,,DOID:0111678,hereditary folate malabsorption,C0342705,C562799,229050,MONDO:0009238,hereditary folate malabsorption,
+BMGC_DS05851,BMG_DS016856,,Gamma aminobutyric acid transaminase deficiency,,,,,,,C0342708,C535407,613163,MONDO:0013166,GABA aminotransaminase deficiency,
+BMGC_DS05852,BMG_DS016864,237945003,Complete deficiency of methylmalonyl-CoA mutase,,,,,,,C0342718,,,MONDO:0017360,vitamin B12-unresponsive methylmalonic acidemia type mut0,Mutase0 methylmalonic acidemia | Complete deficiency of methylmalonyl-CoA mutase | Mutase0 methylmalonic acidaemia | Complete deficiency of methylmalonyl-coenzyme A mutase (disorder) | Complete deficiency of methylmalonyl-coenzyme A mutase | Vitamin B12-unresponsive methylmalonic acidaemia type mut0 | Vitamin B12-unresponsive methylmalonic acidemia type mut0 | MMUT-gene related complete deficiency of methylmalonyl-coenzyme A mutase | Vitamin B12-unresponsive methylmalonic aciduria type mut0
+BMGC_DS05853,BMG_DS016865,237946002,Partial deficiency of methylmalonyl-CoA mutase,,,,,,,C0342719,,,MONDO:0019267,vitamin B12-unresponsive methylmalonic acidemia type mut-,Partial deficiency of methylmalonyl-CoA mutase | Mutase- methylmalonic acidaemia | Mutase- methylmalonic acidemia | Partial deficiency of methylmalonyl-coenzyme A mutase (disorder) | Partial deficiency of methylmalonyl-coenzyme A mutase | Vitamin B12-unresponsive methylmalonic acidaemia type mut- | Vitamin B12-unresponsive methylmalonic acidemia type mut- | MMUT-gene related partial deficiency of methylmalonyl-coenzyme A mutase
+BMGC_DS05854,BMG_DS016870,,"3-@METHYLGLUTACONIC ACIDURIA, TYPE I",,,,,,,C0342727,,600529;250950,MONDO:0009610,3-methylglutaconic aciduria type 1,
+BMGC_DS05855,BMG_DS016872,124327008,Deficiency of mevalonate kinase,,,,,DOID:0050452,mevalonic aciduria,C0342731,,,MONDO:0017708,mevalonate kinase deficiency,Deficiency of mevalonate kinase | Deficiency of mevalonate kinase (disorder) | Mevalonate kinase deficiency
+BMGC_DS05856,BMG_DS016874,237955004,Cytosolic acetoacetyl-CoA thiolase deficiency,,,,,,,C0342735,C536005,614055,MONDO:0013548,acetyl-CoA acetyltransferase-2 deficiency,Cytosolic acetoacetyl-CoA thiolase deficiency | Cytosolic acetoacetyl-coenzyme A thiolase deficiency (disorder) | Cytosolic acetoacetyl-coenzyme A thiolase deficiency
+BMGC_DS05857,BMG_DS016875,237957007,3-Hydroxyisobutyric aciduria,,,,,,,C0342737,C535312,236795,MONDO:0009371,3-hydroxyisobutyric aciduria,3-Hydroxyisobutyric aciduria | 3-Hydroxyisobutyric aciduria (disorder)
+BMGC_DS05858,BMG_DS016876,,Beta-Hydroxyisobutyryl CoA Deacylase Deficiency,,,,,,,C0342738,C562803,250620,MONDO:0009603,3-hydroxyisobutyryl-CoA hydrolase deficiency,
+BMGC_DS05859,BMG_DS016877,237959005,Trimethylaminuria,,,,E72.52,DOID:0080361,trimethylaminuria,C0342739,C536561,MTHU054300,MONDO:0011182,trimethylaminuria,Trimethylaminuria | Fish odour syndrome | Fish odor syndrome | Trimethylaminuria (disorder)
+BMGC_DS05860,BMG_DS016884,,GLYCOGEN STORAGE DISEASE Ic,,,,,DOID:0081331,glycogen storage disease Ic,C0342749,,232240;602671,,,
+BMGC_DS05861,BMG_DS016886,76219003,Generalized glycogen storage disease of infants,,,,,,,C0342751,,,,,"Glycogen storage disease, type II | Glycogen storage disease, type II (disorder)"
+BMGC_DS05862,BMG_DS016888,722343009,Glycogen storage disease type II late onset,,,,,,,C0342753,,,MONDO:0018485,"glycogen storage disease due to acid maltase deficiency, late-onset","Glycogen storage disease type II late onset | Glycogen storage disease due to acid maltase deficiency, late-onset | Alpha-1,4-glucosidase acid deficiency, late onset | Glycogenosis type II, late onset | Pompe disease, late onset | Glycogen storage disease due to acid maltase deficiency, late-onset (disorder)"
+BMGC_DS05863,BMG_DS016898,237980004,D-Glyceric aciduria,,,,,,,C0342765,,220120,MONDO:0009070,D-glyceric aciduria,D-Glyceric aciduria | D-Glyceric aciduria (disorder)
+BMGC_DS05864,BMG_DS016901,237983002,Fumarase deficiency,,,,,DOID:0111261,fumarase deficiency,C0342770,C538191,606812,MONDO:0011730,fumaric aciduria,Fumarase deficiency | Fumarate hydratase deficiency | Fumarate hydratase deficiency (disorder)
+BMGC_DS05865,BMG_DS016907,237995002,Depletion of mitochondrial DNA,,,,,,,C0342782,,,MONDO:0018158,mitochondrial DNA depletion syndrome,Depletion of mitochondrial DNA | Depletion of mitochondrial deoxyribonucleic acid | Depletion of mitochondrial deoxyribonucleic acid (disorder)
+BMGC_DS05866,BMG_DS016908,124166007,Deficiency of butyryl-CoA dehydrogenase,,,,,,,C0342783,,201470,MONDO:0008722,short chain acyl-CoA dehydrogenase deficiency,Deficiency of unsaturated acyl-CoA reductase | Deficiency of butyryl dehydrogenase | Deficiency of butyryl-CoA dehydrogenase | Butyryl-CoA dehydrogenase deficiency | Deficiency of butyryl-CoA dehydrogenase (disorder)
+BMGC_DS05867,BMG_DS016909,,Pearson's marrow-pancreas syndrome,,,,,,,C0342784,C536353,557000,MONDO:0010797,Pearson syndrome,
+BMGC_DS05868,BMG_DS016912,21764004,Renal carnitine transport defect,,,,,DOID:14365,systemic primary carnitine deficiency disease,C0342788,,212140,MONDO:0008919,systemic primary carnitine deficiency disease,Renal carnitine transport defect | Systemic carnitine deficiency | Carnitine transporter deficiency | Carnitine uptake defect | Primary carnitine deficiency | Renal carnitine transport defect (disorder)
+BMGC_DS05869,BMG_DS016913,,Carnitine palmitoyl transferase 2 deficiency,,,,,DOID:0060235,carnitine palmitoyltransferase II deficiency,C0342790,C535589,,MONDO:0015515,carnitine palmitoyltransferase II deficiency,
+BMGC_DS05870,BMG_DS016914,,Carnitine-Acylcarnitine Translocase Deficiency,,,,,DOID:0111585,carnitine-acylcarnitine translocase deficiency,C0342791,C562812,212138,MONDO:0008918,carnitine-acylcarnitine translocase deficiency,
+BMGC_DS05871,BMG_DS016915,,Succinyl-CoA:3-oxoacid CoA transferase deficiency,,,,,,,C0342792,C537527,245050,MONDO:0009492,succinyl-CoA:3-ketoacid CoA transferase deficiency,
+BMGC_DS05872,BMG_DS016916,361203007,Malonic aciduria,,,,,,,C0342793,C535702,248360,MONDO:0009556,malonic aciduria,Malonic aciduria | Malonic aciduria (disorder) | MLYCD-gene related malonic aciduria
+BMGC_DS05873,BMG_DS016919,,Inosine Triphosphatase Deficiency,,,,,,,C0342800,C564127,613850,MONDO:0013461,inosine triphosphatase deficiency,
+BMGC_DS05874,BMG_DS016920,,Thiopurine S methyltranferase deficiency,,,,,DOID:0080172,poor metabolism of thiopurines,C0342801,C536512,610460,MONDO:0012503,thiopurine S-methyltransferase deficiency,
+BMGC_DS05875,BMG_DS016922,238014002,Dihydropyrimidinase deficiency,,,,,DOID:0111629,dihydropyrimidinase deficiency,C0342803,,222748,MONDO:0009111,dihydropyrimidinuria,Dihydrouracil amidohydrolase deficiency | Dihydropyrimidinase deficiency | Dihydropyrimidinase deficiency (disorder)
+BMGC_DS05876,BMG_DS016943,73146005,"Hunter's syndrome, severe form",,,,,,,C0342841,,,MONDO:0016315,"mucopolysaccharidosis type 2, severe form","Hunter's syndrome, severe form | Mucopolysaccharidosis type II severe form | Hunter's syndrome, severe form (disorder) | Hunter syndrome, severe form"
+BMGC_DS05877,BMG_DS016944,5667009,"Hunter's syndrome, mild form",,,,,,,C0342842,,,,,"Hunter's syndrome, mild form | Mucopolysaccharidosis type II mild form | Hunter's syndrome, mild form (disorder) | Hunter syndrome, mild form"
+BMGC_DS05878,BMG_DS016947,62311004,"Mannosidosis, type I",,,,,,,C0342847,,,MONDO:0017732,"alpha-mannosidosis, infantile form","Mannosidosis, type I | Mannosidosis infantile onset | Mannosidosis, severe form | Mannosidosis, type I (disorder) | Infantile mannosidosis"
+BMGC_DS05879,BMG_DS016950,238051008,Sialuria,Sialic Acid Storage Disease,,,,DOID:3659,sialuria,C0342853,D029461,269921,MONDO:0010028,sialuria,Sialuria | Sialuria (disorder)
+BMGC_DS05880,BMG_DS016952,190915002,Coproporphyria,,,,,,,C0342856,C535469,,,,Coproporphyria | Coproporphyria (disorder)
+BMGC_DS05881,BMG_DS016955,238056003,Harderoporphyria,,,,,,,C0342859,C562816,618892,MONDO:0030048,harderoporphyria,Homozygous hereditary coproporphyria | Harderoporphyria | Homozygous hereditary coproporphyria (disorder)
+BMGC_DS05882,BMG_DS016960,,,,,,,,,C0342870,,261515,MONDO:0009855,d-bifunctional protein deficiency,
+BMGC_DS05883,BMG_DS016962,,Glutaric Aciduria III,,,,,,,C0342873,C562818,231690,MONDO:0009283,glutaric acidemia type 3,
+BMGC_DS05884,BMG_DS016968,,Homozygous Familial Hypercholesterolemia,Homozygous Familial Hypercholesterolemia,,,,,,C0342881,D000090542,,MONDO:0018328,homozygous familial hypercholesterolemia,
+BMGC_DS05885,BMG_DS016969,238079002,Familial hypercholesterolemia - heterozygous,,,,,,,C0342882,,,,,Familial hypercholesterolaemia - heterozygous | Familial hypercholesterolemia - heterozygous | Familial hypercholesterolemia - heterozygous (disorder)
+BMGC_DS05886,BMG_DS016970,,Cholesteryl Ester Transfer Protein Deficiency,,,,,DOID:0111369,hyperalphalipoproteinemia 1,C0342883,C564591,,MONDO:0015903,hyperalphalipoproteinemia,
+BMGC_DS05887,BMG_DS016975,,Fish-Eye Disease,Lecithin Cholesterol Acyltransferase Deficiency,,,,,,C0342895,D007863,136120,MONDO:0007620,fish eye disease,
+BMGC_DS05888,BMG_DS016976,238095002,Apolipoprotein A-I deficiency,,,,,,,C0342898,,,,,Apolipoprotein A-I deficiency | Apolipoprotein A-I deficiency (disorder)
+BMGC_DS05889,BMG_DS016978,,,,,,,DOID:0090019,sitosterolemia 1,C0342907,,,MONDO:0008863,sitosterolemia,
+BMGC_DS05890,BMG_DS016988,238128006,Pantothenic acid deficiency,,5B7Z,Unspecified undernutrition,E53.8,,,C0342938,,,,,Pantothenic acid deficiency | Pantothenic acid deficiency (disorder) | Deficiency of pantothenic acid
+BMGC_DS05891,BMG_DS017012,275441009,Superficial bacterial infection of skin,,,,,,,C0342985,,,,,Superficial bacterial infection of skin | Superficial bacterial infection of skin (disorder)
+BMGC_DS05892,BMG_DS017036,,Complement component 5 deficiency,,,,,DOID:8158,complement component 5 deficiency,C0343047,C537005,609536,MONDO:0012295,complement component 5 deficiency,
+BMGC_DS05893,BMG_DS017039,,Guttate Psoriasis,Guttate Psoriasis,,,,,,C0343052,D000098650,,MONDO:0023297,guttate psoriasis,
+BMGC_DS05894,BMG_DS017041,238612002,Generalized pustular psoriasis,,EA90.40,Generalised pustular psoriasis,L40.1,DOID:0080474,pustular psoriasis 14,C0343055,,,MONDO:0100491,generalized pustular psoriasis,Generalised pustular psoriasis | Generalized pustular psoriasis | Generalized pustular psoriasis (disorder) | Generalized pustular psoriasis of von Zumbusch | Generalised pustular psoriasis of von Zumbusch | Acute generalized pustular psoriasis | Acute generalised pustular psoriasis
+BMGC_DS05895,BMG_DS017042,,,,,,,,,C0343057,,,MONDO:0000136,keratosis follicularis spinulosa decalvans,
+BMGC_DS05896,BMG_DS017045,201263000;7632005,Dermatographic urticaria,,EB01.0,Dermographism,L50.3,DOID:743,dermatographia,C0343065,,,,,(Dermatographic urticaria) or (factitial urticaria) | Dermatographic urticaria | Factitial urticaria | (Dermatographic urticaria) or (factitial urticaria) (disorder) | Dermatographic urticaria | Dermatographia | Ebbecke's reaction | Dermagraphy | Autographism | Skin writing | Factitial urticaria | Dermographia | Urticaria factitia | Dermatography | Dermographism | Dermographic urticaria | Dermatographic urticaria (disorder) | Dermatographism
+BMGC_DS05897,BMG_DS017046,238687000,Familial cold urticaria,,,,M04.2,,,C0343068,,,MONDO:0018768,familial cold autoinflammatory syndrome,Familial cold urticaria | Familial cold urticaria (disorder) | Familial cold autoinflammatory syndrome | FCU - familial cold urticaria | FCAS - familial cold autoinflammatory syndrome
+BMGC_DS05898,BMG_DS017049,,,,,,,,,C0343073,,,MONDO:0008686,isolated familial wooly hair disorder,
+BMGC_DS05899,BMG_DS017055,,,,,,,,,C0343079,,157400,MONDO:0008001,"milia, multiple eruptive",
+BMGC_DS05900,BMG_DS017057,238762002;201299005,Livedoid vasculitis,,EF50,Livedoid vasculopathy,L95.0,DOID:0040099,livedoid vasculitis,C0343081,,,MONDO:0025514,livedoid vasculopathy,Livedoid vasculitis | Idiopathic atrophic blanche | White atrophy | Livedoid vasculitis (disorder) | Livedoid vasculitis | Livedoid vasculitis (disorder)
+BMGC_DS05901,BMG_DS017058,,,,,,,DOID:2495,senile angioma,C0343082,,,MONDO:0002323,cherry hemangioma,
+BMGC_DS05902,BMG_DS017060,,Capillary Leak Syndrome,Capillary Leak Syndrome,,,,DOID:14400,capillary leak syndrome,C0343084,D019559,,MONDO:0001956,capillary leak syndrome,
+BMGC_DS05903,BMG_DS017062,,,,,,,,,C0343094,,173700,MONDO:0008261,"hereditary sclerosing poikiloderma, Weary type",
+BMGC_DS05904,BMG_DS017063,,Nodular Elastoidosis,Facial Dermatoses,,,,,,C0343097,D005148,,,,
+BMGC_DS05905,BMG_DS017067,,Flynn Aird syndrome,,,,,,,C0343108,C537066,136300,MONDO:0007624,Flynn-Aird syndrome,
+BMGC_DS05906,BMG_DS017068,,Naegeli syndrome,,,,,DOID:0111528,Naegeli-Franceschetti-Jadassohn syndrome,C0343111,C538331,161000,MONDO:0008059,Naegeli-Franceschetti-Jadassohn syndrome,
+BMGC_DS05907,BMG_DS017070,,,,,,,,,C0343114,,,MONDO:0019311,wooly hair nevus,
+BMGC_DS05908,BMG_DS017071,,,,,,,DOID:3666,solitary mastocytoma of the skin,C0343115,,,MONDO:0019314,cutaneous mastocytoma,
+BMGC_DS05909,BMG_DS017092,239926000,Cutaneous polyarteritis nodosa,,,,,,,C0343190,,,MONDO:0018592,cutaneous polyarteritis nodosa,Cutaneous polyarteritis nodosa | Cutaneous livedo with nodules | Nodular livedo | Cutaneous polyarteritis nodosa (disorder)
+BMGC_DS05910,BMG_DS017103,1149219001;400054000;239942007,Systemic rheumatoid vasculitis,,,,,,,C0343203,,,,,Rheumatoid arthritis with systemic vasculitis | Rheumatoid arthritis with systemic vasculitis (disorder) | Systemic rheumatoid vasculitis | Rheumatoid vasculitis | Rheumatoid arthritis with vasculitis (disorder) | Rheumatoid arthritis with vasculitis | Systemic rheumatoid vasculitis | Systemic rheumatoid vasculitis (disorder)
+BMGC_DS05911,BMG_DS017106,239945009,Hypocomplementemic urticarial vasculitis,,,,,,,C0343206,,,MONDO:0018227,hypocomplementemic urticarial vasculitis,Hypocomplementaemic vasculitis | Hypocomplementaemic urticarial vasculitis | Hypocomplementemic vasculitis | Hypocomplementemic urticarial vasculitis | Hypocomplementemic urticarial vasculitis (disorder)
+BMGC_DS05912,BMG_DS017150,,,,,,,,,C0343284,,,MONDO:0022723,chondrodysplasia,
+BMGC_DS05913,BMG_DS017158,43424001,Tetanus neonatorum,,,,A33,DOID:13521,tetanus neonatorum,C0343312,,,MONDO:0001737,tetanus neonatorum,Tetanus neonatorum | Tetanus neonatorum (disorder)
+BMGC_DS05914,BMG_DS017175,266078006;186142005,Pseudomonas gastrointestinal tract infection,,,,,,,C0343337,,,,,Pseudomonas gastrointestinal tract infection | Pseudomonas gastrointestinal tract infection (disorder) | Pseudomonas: [GIT infection] or [pyocyanea diarrhoea] | Pseudomonas gastrointestinal tract infection | Pseudomonas: [GIT infection] or [pyocyanea diarrhea] | Diarrhea due to Pseudomonas pyocyanea | Diarrhoea due to Pseudomonas pyocyanea | Pseudomonas: [GIT infection] or [pyocyanea diarrhoea] (disorder)
+BMGC_DS05915,BMG_DS017201,89538001,Helicobacter-associated gastritis,,,,,,,C0343378,,,,,Helicobacter-associated gastritis | Helicobacter-associated gastritis (disorder)
+BMGC_DS05916,BMG_DS017208,389981005;186431008,Clostridium difficile infection,,,,,,,C0343386,,,,,Clostridium difficile infection | Clostridium difficile infection (disorder) | Clostridium difficile infection | Clostridioides difficile infection | Infection caused by Clostridioides difficile (disorder) | Infection caused by Clostridioides difficile
+BMGC_DS05917,BMG_DS017218,240372001,Cyclosporiasis,Cyclosporiasis,,,A07.4,DOID:12750,cyclosporiasis,C0343398,D021866,,MONDO:0005725,cyclosporiasis,Cyclosporiasis | Cyclosporiasis (disorder)
+BMGC_DS05918,BMG_DS017221,266096002,Methicillin resistant Staphylococcus aureus infection,,,,,,,C0343401,,,MONDO:0100073,methicillin-resistant staphylococcus aureus infectious disease,Methicillin resistant Staphylococcus aureus infection (disorder) | Methicillin resistant Staphylococcus aureus infection | Infection due to Methicillin resistant Staphylococcus aureus | MRSA (Methicillin resistant Staphylococcus aureus) infection
+BMGC_DS05919,BMG_DS017222,186435004,Bacterial infection caused by Klebsiella pneumoniae,,,,,,,C0343402,,,,,Friedlander's bacillus infection | Friedlander's bacillus infection (disorder) | Friedlander bacillus infection | Bacterial infection caused by Klebsiella pneumoniae
+BMGC_DS05920,BMG_DS017270,240411003,Erythema nodosum leprosum,,,,,,,C0343467,,,,,ENL - Erythema nodosum leprosum | Erythema nodosum leprosum | Erythema nodosum leprosum (disorder)
+BMGC_DS05921,BMG_DS017285,154301006;186357007,Streptococcal sore throat with scarlatina,,,,,DOID:8596,scarlet fever,C0343487,,,,,Streptococcal sore throat with scarlatina | Streptococcal sore throat with scarlatina (disorder)
+BMGC_DS05922,BMG_DS017296,186410005;266093005,Gas gangrene caused by clostridium perfringens,,,,,,,C0343500,,,,,Clostridium perfringens infection | Gas gangrene caused by clostridium perfringens | Clostridium (& [perfringens] or [welchii]: [infection] or [gas gangrene] | Gas gangrene caused by clostridium welchii | Clostridium (& [perfringens] or [welchii]: [infection] or [gas gangrene] (disorder) | Gas gangrene caused by clostridium perfringens | Gas gangrene caused by clostridium welchii | Gas gangrene caused by clostridium perfringens (disorder)
+BMGC_DS05923,BMG_DS017322,,Pontiac Fever,Legionnaires' Disease,,,,,,C0343528,D007877,,MONDO:0020487,Pontiac fever,
+BMGC_DS05924,BMG_DS017325,240451000,Streptococcal toxic shock syndrome,,,,,,,C0343532,,,MONDO:0020544,streptococcal toxic-shock syndrome,Streptococcal toxic shock syndrome | Streptococcal toxic shock syndrome (disorder)
+BMGC_DS05925,BMG_DS017417,75003008;186751006;240532009,Human papilloma virus infection,,,,,,,C0343641,,,MONDO:0005161,human papilloma virus infection,Papovavirus infection subgroup A | Papovavirus infection subgroup A (disorder) | Human papilloma virus infection | Human papilloma virus infection (disorder) | Human papilloma virus infection | Human papillomavirus infection (disorder) | Human papillomavirus infection | HPV (Human papillomavirus) infection | HPV (Human papillomavirus) disease
+BMGC_DS05926,BMG_DS017469,266138002;186927008,Gonococcal synovitis or tenosynovitis,,,,,DOID:13454,gonococcal synovitis,C0343714,,,,,Gonococcal synovitis or tenosynovitis | Gonococcal synovitis or tenosynovitis (disorder) | Gonococcal synovitis &/or tenosynovitis | Gonococcal teno-synovitis | Gonococcal synovitis | Gonococcal synovitis or tenosynovitis | Gonococcal tenosynovitis | Gonococcal synovitis &/or tenosynovitis (disorder)
+BMGC_DS05927,BMG_DS017482,154364000;186689006;266114001,Perianal warts,,,,,,,C0343730,,,,,Perianal warts | Perianal warts (disorder) | Warts: [perianal] or [anal] | Anal warts | Perianal warts | Warts: [perianal] or [anal] (disorder)
+BMGC_DS05928,BMG_DS017498,111880001,Acute HIV infection,,,,,,,C0343752,,,,,Acute HIV infection | Acute human immunodeficiency virus seroconversion illness | Acute human immunodeficiency virus infection | Acute human immunodeficiency virus infection (disorder)
+BMGC_DS05929,BMG_DS017500,,HIV Wasting Syndrome,HIV Wasting Syndrome,,,,,,C0343755,D019247,,MONDO:0005797,HIV wasting syndrome,
+BMGC_DS05930,BMG_DS017503,240614000;186772009,American tick typhus,,,,,,,C0343759,,,,,American tick typhus | American tick typhus (disorder) | RMSF - Rocky Mountain spotted fever | Rocky Mountain spotted fever | Rocky Mountain spotted fever (disorder) | Rocky Mountain tick fever | Sao Paulo fever | Brazilian spotted fever | American tick typhus
+BMGC_DS05931,BMG_DS017559,88037009,Tertiary lesion of yaws,,,,,,,C0343833,,,MONDO:0042452,tertiary lesion of yaws,Tertiary lesion of yaws | Tertiary stage of yaws | Tertiary lesion of yaws (disorder) | Tertiary yaws
+BMGC_DS05932,BMG_DS017560,266147005,Bone and/or joint yaws lesions,,,,,DOID:10568,early yaws,C0343834,,,,,Bone and joint yaws lesions | Bone and/or joint yaws lesions (disorder) | Bone and/or joint yaws lesions
+BMGC_DS05933,BMG_DS017580,240704003;187006006,Pharyngeal candidiasis,,,,,,,C0343861,,,,,Pharyngeal candidiasis | Candidosis of pharynx | Pharyngeal thrush | Pharyngeal candidiasis (disorder) | Oral candidiasis | Oral moniliasis | Pharyngeal candidiasis | Candidiasis: [oral and oesophagus] or [pharyngeal] | Candidiasis: [oral and esophagus] or [pharyngeal] | Candidiasis of mouth and esophagus | Monilia of mouth and esophagus | Thrush of mouth and esophagus | Monilia of mouth and oesophagus | Candidiasis of mouth and oesophagus | Thrush of mouth and oesophagus | Candidiasis: [oral and oesophagus] or [pharyngeal] (disorder)
+BMGC_DS05934,BMG_DS017602,84679006,Gastrointestinal candidiasis,,,,,,,C0343886,,,,,Gastrointestinal candidiasis | Gastrointestinal candidiasis (disorder) | Candidiasis of intestine
+BMGC_DS05935,BMG_DS017646,240761008,Trichosporonosis,Trichosporonosis,,,,DOID:0050290,trichosporonosis,C0343939,D060586,,MONDO:0000306,trichosporonosis,Trichosporonosis | Trichosporonosis (disorder)
+BMGC_DS05936,BMG_DS017647,,Disseminated Trichosporonosis,Trichosporonosis,,,,DOID:0050290,trichosporonosis,C0343941,D060586,,,,
+BMGC_DS05937,BMG_DS017666,240782002,Entomophthoramycosis,Zygomycosis,,,,,,C0343961,D020096,,,,Entomophthoramycosis | Infection by Entomophthora | Entomophthoramycosis (disorder)
+BMGC_DS05938,BMG_DS017792,,See-Saw Nystagmus,"Nystagmus, Pathologic",,,,,,C0344243,D009759,,,,
+BMGC_DS05939,BMG_DS017802,65545003,Bullous retinoschisis,,,,,DOID:12108,bullous retinoschisis,C0344289,,,MONDO:0001435,bullous retinoschisis,"Bullous retinoschisis | Bullous retinoschisis (disorder) | Peripheral retinoschisis, retinal cysts"
+BMGC_DS05940,BMG_DS017803,247182006,Vitreoretinal degeneration,,,,,,,C0344290,,MTHU002188,MONDO:0020248,vitreoretinal degeneration,Vitreoretinal degeneration | Vitreoretinal degeneration (disorder)
+BMGC_DS05941,BMG_DS017805,47638000;247199007,Choroidal sclerosis,,,,,DOID:980,choroidal sclerosis,C0344297,C535358,MTHU006953,MONDO:0004885,choroidal sclerosis,Choroidal degeneration | Choroidal sclerosis | Choroidal degeneration (disorder) | Choroidal sclerosis | Choroidal sclerosis (finding)
+BMGC_DS05942,BMG_DS017808,,,,,,,DOID:605,flying phobia,C0344318,,,MONDO:0003748,flying phobia,
+BMGC_DS05943,BMG_DS017824,251159007,"Ventricular tachycardia, polymorphic",,,,,,,C0344432,,,MONDO:0020575,polymorphic ventricular tachycardia,"Ventricular tachycardia, polymorphic | Ventricular tachycardia, polymorphic (disorder)"
+BMGC_DS05944,BMG_DS017826,,,,,,,DOID:5719,adrenal medulla cancer,C0344456,,,MONDO:0003606,adrenal medulla cancer,
+BMGC_DS05945,BMG_DS017827,,,,,,,DOID:297,pleomorphic adenoma carcinoma,C0344460,,,MONDO:0002472,carcinoma ex pleomorphic adenoma,
+BMGC_DS05946,BMG_DS017829,,Spinal intradural arachnoid cysts,,,,,,,C0344485,C536878,182990,MONDO:0008454,spinal intradural arachnoid cysts,
+BMGC_DS05947,BMG_DS017833,,,,,,,,,C0344516,,,MONDO:0020355,coloboma of eye lens,
+BMGC_DS05948,BMG_DS017834,,,,,,,,,C0344523,,,MONDO:0020374,cerulean cataract,
+BMGC_DS05949,BMG_DS017836,,,,,,,,,C0344529,,,MONDO:0000733,cornea plana,
+BMGC_DS05950,BMG_DS017837,,,,,,,DOID:0060305,megalocornea,C0344530,,249300,MONDO:0009576,megalocornea,
+BMGC_DS05951,BMG_DS017838,,,,,,,,,C0344542,,106210,MONDO:0024507,aniridia 1,
+BMGC_DS05952,BMG_DS017839,,,,,,,,,C0344543,,617141,MONDO:0014937,aniridia 2,
+BMGC_DS05953,BMG_DS017841,,,,,,,,,C0344559,,604229,MONDO:0011414,Peters anomaly,
+BMGC_DS05954,BMG_DS017851,,,,,,,,,C0344688,,601466,MONDO:0011089,patent ductus venosus,
+BMGC_DS05955,BMG_DS017853,,,,,,,,,C0344697,,,MONDO:0020429,cor triatriatum dexter,
+BMGC_DS05956,BMG_DS017859,,,,,,,,,C0344724,,,MONDO:0020434,"atrial septal defect, ostium secundum type",
+BMGC_DS05957,BMG_DS017860,,,,,,,,,C0344730,,,MONDO:0020436,"atrial septal defect, sinus venosus type",
+BMGC_DS05958,BMG_DS017863,,,,,,,,,C0344760,,,MONDO:0015249,mitral atresia disorder,
+BMGC_DS05959,BMG_DS017879,253541009,Left cardiac ventricular dilatation,,,,,,,C0344911,,,,,Dilatation of left cardiac ventricle (disorder) | Dilatation of left cardiac ventricle | Left cardiac ventricular dilatation
+BMGC_DS05960,BMG_DS017883,204348000;268180007,Right hypoplastic heart syndrome,,,,,DOID:0070315,hypoplastic right heart syndrome,C0344963,,,MONDO:0020291,hypoplastic right heart syndrome,(Right hypoplastic heart syndrome) or (pseudotruncus arteriosus) | Pseudotruncus arteriosus | Right hypoplastic heart syndrome | (Right hypoplastic heart syndrome) or (pseudotruncus arteriosus) (disorder) | Right hypoplastic heart syndrome | Pseudotruncus arteriosus | Right hypoplastic heart syndrome (disorder)
+BMGC_DS05961,BMG_DS017884,,,,,,,,,C0344975,,265150,MONDO:0009931,pulmonary atresia-intact ventricular septum syndrome,
+BMGC_DS05962,BMG_DS017885,,,,,,,,,C0344976,,178370,MONDO:0008343,pulmonary atresia with ventricular septal defect,
+BMGC_DS05963,BMG_DS017889,,,,,,,DOID:14037,aorta atresia,C0345010,,,MONDO:0001863,aorta atresia,
+BMGC_DS05964,BMG_DS017891,253631001,Peripheral pulmonary artery stenosis,,,,,,,C0345030,,MTHU014956,,,PPS - Peripheral pulmonary stenosis | Peripheral pulmonary artery stenosis | Peripheral pulmonary artery stenosis (disorder)
+BMGC_DS05965,BMG_DS017894,,,,,,,,,C0345050,,607086,MONDO:0024559,"aortic aneurysm, familial thoracic 1",
+BMGC_DS05966,BMG_DS017905,,,,,,,DOID:0080833,laryngomalacia,C0345160,,,,,
+BMGC_DS05967,BMG_DS017916,,,,,,,,,C0345240,,202550,MONDO:0008738,"aganglionosis, total intestinal",
+BMGC_DS05968,BMG_DS017923,,,,,,,,,C0345326,,,MONDO:0006904,phimosis,
+BMGC_DS05969,BMG_DS017925,,,,,,,,,C0345345,,,MONDO:0015195,atresia of urethra,
+BMGC_DS05970,BMG_DS017929,,,,,,,,,C0345375,,,MONDO:0016032,femoral agenesis/hypoplasia,
+BMGC_DS05971,BMG_DS017931,,"OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3",,,,,DOID:0110941,autosomal recessive osteopetrosis 3,C0345407,,259730;611492,MONDO:0009818,autosomal recessive osteopetrosis 3,
+BMGC_DS05972,BMG_DS017932,,,,,,,,,C0345408,,119900,MONDO:0007343,isolated congenital digital clubbing,
+BMGC_DS05973,BMG_DS017933,,,,,,,,,C0345419,,219250,MONDO:0009055,cutis marmorata telangiectatica congenita,
+BMGC_DS05974,BMG_DS017934,,,,,,,,,C0345424,,120450,MONDO:0007358,"comedones, familial Dyskeratotic",
+BMGC_DS05975,BMG_DS017949,,,,,,,DOID:5099,middle ear cancer,C0345617,,,MONDO:0021366,neoplasm of middle ear,
+BMGC_DS05976,BMG_DS017952,,,,,,,DOID:1364,ethmoidal sinus benign neoplasm,C0345668,,,MONDO:0001764,ethmoidal sinus neoplasm,
+BMGC_DS05977,BMG_DS017954,,,,,,,DOID:1361,frontal sinus benign neoplasm,C0345672,,,MONDO:0001757,frontal sinus neoplasm,
+BMGC_DS05978,BMG_DS017956,,,,,,,DOID:6947,sphenoidal sinus benign neoplasm,C0345676,,,MONDO:0004047,sphenoidal sinus neoplasm,
+BMGC_DS05979,BMG_DS017958,,,,,,,DOID:2597,glottis neoplasm,C0345713,,,MONDO:0002353,glottis neoplasm,
+BMGC_DS05980,BMG_DS017959,,,,,,,DOID:8002,supraglottis neoplasm,C0345726,,,MONDO:0004427,supraglottis neoplasm,
+BMGC_DS05981,BMG_DS017960,,,,,,,DOID:10069,subglottis benign neoplasm,C0345746,,,MONDO:0000933,subglottis neoplasm,
+BMGC_DS05982,BMG_DS017963,,,,,,,DOID:6700,gastric fundus carcinoma,C0345799,,,MONDO:0003970,gastric fundus carcinoma,
+BMGC_DS05983,BMG_DS017965,,,,,,,DOID:6705,gastric body carcinoma,C0345804,,,MONDO:0003972,gastric body carcinoma,
+BMGC_DS05984,BMG_DS017967,,,,,,,DOID:7505,small intestine benign neoplasm,C0345832,,,MONDO:0004251,small intestine neoplasm,
+BMGC_DS05985,BMG_DS017970,,,,,,,DOID:2780,rectosigmoid junction neoplasm,C0345873,,,MONDO:0002423,rectosigmoid junction neoplasm,
+BMGC_DS05986,BMG_DS017972,,,,,,,,,C0345893,,174900,MONDO:0017380,juvenile polyposis syndrome,
+BMGC_DS05987,BMG_DS017974,,,,,,,DOID:3571,liver cancer,C0345904,,,MONDO:0002691,liver cancer,
+BMGC_DS05988,BMG_DS017975,,,,,,,DOID:4928,intrahepatic cholangiocarcinoma,C0345905,,,MONDO:0003210,intrahepatic cholangiocarcinoma,
+BMGC_DS05989,BMG_DS017976,,,,,,,DOID:270,liver sarcoma,C0345906,,,MONDO:0002397,liver sarcoma,
+BMGC_DS05990,BMG_DS017977,,,,,,,DOID:268,liver angiosarcoma,C0345907,,,MONDO:0002387,liver angiosarcoma,
+BMGC_DS05991,BMG_DS017981,,,,,,,DOID:0050625,biliary tract benign neoplasm,C0345913,,,MONDO:0021385,extrahepatic bile duct neoplasm,
+BMGC_DS05992,BMG_DS017983,,,,,,,DOID:10022,ampulla of Vater benign neoplasm,C0345916,,,MONDO:0000921,ampulla of vater neoplasm,
+BMGC_DS05993,BMG_DS017986,,,,,,,DOID:4875,trachea adenoid cystic carcinoma,C0345945,,,MONDO:0006471,tracheal adenoid cystic carcinoma,
+BMGC_DS05994,BMG_DS017987,,,,,,,DOID:12003,trachea squamous cell carcinoma,C0345946,,,MONDO:0001419,trachea squamous cell carcinoma,
+BMGC_DS05995,BMG_DS017988,,,,,,,DOID:4556,lung large cell carcinoma,C0345958,,,MONDO:0003050,lung large cell carcinoma,
+BMGC_DS05996,BMG_DS017989,,,,,,,DOID:7267,lung clear cell carcinoma,C0345959,,,,,
+BMGC_DS05997,BMG_DS017990,,,,,,,DOID:5583,lung giant cell carcinoma,C0345960,,,MONDO:0006275,lung giant cell carcinoma,
+BMGC_DS05998,BMG_DS017992,,,,,,,DOID:5386,lung adenoma,C0345964,,,MONDO:0003422,lung adenoma,
+BMGC_DS05999,BMG_DS017993,,,,,,,DOID:1790,malignant mesothelioma,C0345967,,156240,MONDO:0006292,malignant mesothelioma,
+BMGC_DS06000,BMG_DS017996,,,,,,,DOID:8288,clear cell squamous cell skin carcinoma,C0345978,,,MONDO:0004523,clear cell squamous cell skin carcinoma,
+BMGC_DS06001,BMG_DS017997,,,,,,,DOID:7643,acantholytic squamous cell skin carcinoma,C0345979,,,MONDO:0004316,acantholytic squamous cell skin carcinoma,
+BMGC_DS06002,BMG_DS017999,,,,,,,DOID:5585,Ferguson-Smith tumor,C0345982,,,,,
+BMGC_DS06003,BMG_DS018000,,,,,,,DOID:7380,squamous cell papilloma of skin,C0345983,,,MONDO:0004204,squamous cell skin papilloma,
+BMGC_DS06004,BMG_DS018002,,,,,,,DOID:2433,epidermal appendage tumor,C0345988,,,MONDO:0002297,epidermal appendage tumor,
+BMGC_DS06005,BMG_DS018006,,,,,,,DOID:4322,pilar sheath acanthoma,C0346005,,,MONDO:0006907,pilar sheath acanthoma,
+BMGC_DS06006,BMG_DS018007,,,,,,,DOID:8426,follicular infundibulum tumor,C0346006,,,MONDO:0004560,follicular infundibulum tumor,
+BMGC_DS06007,BMG_DS018008,,Birt-Hogg-Dube Syndrome,Birt-Hogg-Dube Syndrome,,,,DOID:0050676,Birt-Hogg-Dube syndrome,C0346010,D058249,135150,MONDO:0800445;MONDO:0800444,Birt-Hogg-Dube syndrome 1 | Birt-Hogg-Dube syndrome,
+BMGC_DS06008,BMG_DS018009,,,,,,,DOID:4291,fibroepithelial basal cell carcinoma,C0346013,,,MONDO:0002948,skin fibroepithelial basal cell carcinoma,
+BMGC_DS06009,BMG_DS018010,,,,,,,DOID:4871,cutaneous adenocystic carcinoma,C0346017,,,MONDO:0003180,cutaneous adenocystic carcinoma,
+BMGC_DS06010,BMG_DS018011,,,,,,,DOID:4683,cutaneous mucoepidermoid carcinoma,C0346019,,,MONDO:0003091,cutaneous mucoepidermoid carcinoma,
+BMGC_DS06011,BMG_DS018013,,,,,,,DOID:2079,eccrine mixed tumor of skin,C0346026,,,MONDO:0002200,eccrine mixed tumor of skin,
+BMGC_DS06012,BMG_DS018016,,,,,,,DOID:2438,dermis tumor,C0346041,,,MONDO:0002300,dermis tumor,
+BMGC_DS06013,BMG_DS018017,,,,,,,DOID:4418,cutaneous fibrous histiocytoma,C0346049,,,,,
+BMGC_DS06014,BMG_DS018018,,,,,,,DOID:5769,verruciform xanthoma of skin,C0346054,,,MONDO:0003640,verruciform xanthoma of skin,
+BMGC_DS06015,BMG_DS018020,,,,,,,DOID:2410,skin granular cell tumor,C0346060,,,MONDO:0002291,cutaneous granular cell tumor,
+BMGC_DS06016,BMG_DS018021,,,,,,,DOID:2425,cutaneous ganglioneuroma,C0346063,,,MONDO:0002293,cutaneous ganglioneuroma,
+BMGC_DS06017,BMG_DS018022,,,,,,,DOID:5132,leiomyoma cutis,C0346064,,,MONDO:0003291,leiomyoma cutis,
+BMGC_DS06018,BMG_DS018024,,,,,,,DOID:5273,cutaneous leiomyosarcoma,C0346067,,,MONDO:0003362,cutaneous leiomyosarcoma,
+BMGC_DS06019,BMG_DS018026,,,,,,,,,C0346072,,112200,MONDO:0007203,blue rubber bleb nevus,
+BMGC_DS06020,BMG_DS018027,,,,,,,,,C0346073,,607859,MONDO:0011927,tufted angioma,
+BMGC_DS06021,BMG_DS018028,,,,,,,DOID:479,angiokeratoma,C0346075,,,,,
+BMGC_DS06022,BMG_DS018030,,,,,,,DOID:4517,skin angiosarcoma,C0346081,,,MONDO:0003029,skin angiosarcoma,
+BMGC_DS06023,BMG_DS018032,,,,,,,DOID:2430,skin glomus tumor,C0346083,,,MONDO:0002295,skin glomus tumor,
+BMGC_DS06024,BMG_DS018036,,,,,,,,,C0346104,,301845,MONDO:0010535,Bazex-Dupre-Christol syndrome,
+BMGC_DS06025,BMG_DS018037,,,,,,,DOID:1788,peritoneal mesothelioma,C0346109,,,MONDO:0005512,malignant peritoneal mesothelioma,
+BMGC_DS06026,BMG_DS018038,,,,,,,DOID:6201,pericardial mesothelioma,C0346110,,,,,
+BMGC_DS06027,BMG_DS018041,,,,,,,DOID:3315,lipoma,C0346118,,,MONDO:0044983,benign lipomatous neoplasm,
+BMGC_DS06028,BMG_DS018042,,,,,,,DOID:7578,breast scirrhous carcinoma,C0346151,,,MONDO:0004288,scirrhous breast carcinoma,
+BMGC_DS06029,BMG_DS018043,,,,,,,,,C0346153,,114480,MONDO:0016419,hereditary breast carcinoma,
+BMGC_DS06030,BMG_DS018044,,,,,,,DOID:3016,breast malignant phyllodes tumor,C0346154,,,MONDO:0002489,malignant breast phyllodes tumor,
+BMGC_DS06031,BMG_DS018046,,,,,,,DOID:7223,breast giant fibroadenoma,C0346157,,,MONDO:0004150,breast giant fibroadenoma,
+BMGC_DS06032,BMG_DS018047,,,,,,,DOID:1618,breast fibroadenoma,C0346158,,,,,
+BMGC_DS06033,BMG_DS018048,,,,,,,,,C0346161,,,MONDO:0018364,malignant epithelial tumor of ovary,
+BMGC_DS06034,BMG_DS018049,,,,,,,DOID:5828,endometrioid ovary carcinoma,C0346163,,,MONDO:0006335,ovarian endometrioid adenocarcinoma,
+BMGC_DS06035,BMG_DS018052,,,,,,,,,C0346167,,,MONDO:0006477,undifferentiated ovarian carcinoma,
+BMGC_DS06036,BMG_DS018053,,,,,,,DOID:3269,ovarian cystadenoma,C0346169,,,MONDO:0005183,ovarian cystadenoma,
+BMGC_DS06037,BMG_DS018054,,,,,,,DOID:3267,mucinous ovarian cystadenoma,C0346172,,,MONDO:0002583,mucinous ovarian cystadenoma,
+BMGC_DS06038,BMG_DS018057,,,,,,,DOID:2155,malignant ovarian germ cell neoplasm,C0346180,,,MONDO:0018171,malignant germ cell tumor of ovary,
+BMGC_DS06039,BMG_DS018058,,,,,,,DOID:5550,choriocarcinoma of ovary,C0346181,,,MONDO:0003507,choriocarcinoma of ovary,
+BMGC_DS06040,BMG_DS018059,,,,,,,DOID:6331,immature teratoma of ovary,C0346182,,,MONDO:0018369,immature ovarian teratoma,
+BMGC_DS06041,BMG_DS018060,,,,,,,DOID:5681,ovarian embryonal carcinoma,C0346183,,,MONDO:0003581,ovarian embryonal carcinoma,
+BMGC_DS06042,BMG_DS018061,,,,,,,DOID:5511,dysgerminoma of ovary,C0346185,,,MONDO:0003481,dysgerminoma of ovary,
+BMGC_DS06043,BMG_DS018062,,,,,,,DOID:5350,ovarian endodermal sinus tumor,C0346188,,,MONDO:0006344,ovarian yolk sac tumor,
+BMGC_DS06044,BMG_DS018064,,,,,,,DOID:5172,endometrium carcinoma in situ,C0346191,,,MONDO:0003315,endometrium carcinoma in situ,
+BMGC_DS06045,BMG_DS018065,,,,,,,DOID:5729,intravenous leiomyomatosis,C0346200,,,MONDO:0003614,intravenous leiomyomatosis,
+BMGC_DS06046,BMG_DS018066,,,,,,,DOID:5636,cervical adenosquamous carcinoma,C0346202,,,MONDO:0006134,cervical adenosquamous carcinoma,
+BMGC_DS06047,BMG_DS018069,,,,,,,DOID:512,epididymal neoplasm,C0346239,,,MONDO:0003283,epididymal neoplasm,
+BMGC_DS06048,BMG_DS018070,,,,,,,DOID:4463,multilocular clear cell renal cell carcinoma,C0346249,,,MONDO:0003010,multilocular clear cell renal cell carcinoma,
+BMGC_DS06049,BMG_DS018071,,,,,,,DOID:4242,kidney sarcoma,C0346251,,,MONDO:0002930,kidney sarcoma,
+BMGC_DS06050,BMG_DS018072,,,,,,,DOID:6245,renal oncocytoma,C0346255,,,MONDO:0003825,kidney oncocytoma,
+BMGC_DS06051,BMG_DS018073,,,,,,,DOID:262,kidney hemangiopericytoma,C0346256,,,,,
+BMGC_DS06052,BMG_DS018074,,,,,,,DOID:5977,renal pelvis benign neoplasm,C0346260,,,MONDO:0003719,renal pelvis neoplasm,
+BMGC_DS06053,BMG_DS018077,,,,,,,DOID:5648,choroid plexus carcinoma,C0346289,,,MONDO:0002681,choroid plexus cancer,
+BMGC_DS06054,BMG_DS018079,,,,,,,DOID:3184,spinal cord oligodendroglioma,C0346295,,,MONDO:0002541,spinal cord oligodendroglioma,
+BMGC_DS06055,BMG_DS018080,,,,,,,DOID:4916,pituitary carcinoma,C0346300,,,MONDO:0017582,pituitary adenocarcinoma,
+BMGC_DS06056,BMG_DS018081,,,,,,,DOID:6255,growth hormone secreting pituitary adenoma,C0346302,,,,,
+BMGC_DS06057,BMG_DS018082,,,,,,,DOID:6275,TSH producing pituitary tumor,C0346303,,,MONDO:0019611,TSH-secreting pituitary adenoma,
+BMGC_DS06058,BMG_DS018086,,,,,,,DOID:4992,optic nerve glioma,C0346326,,,MONDO:0003235,optic nerve glioma,
+BMGC_DS06059,BMG_DS018087,,,,,,,DOID:5632,optic nerve sheath meningioma,C0346328,,,MONDO:0003557,optic nerve sheath meningioma,
+BMGC_DS06060,BMG_DS018089,,,,,,,DOID:2814,malignant neoplasm of acoustic nerve,C0346331,,,MONDO:0002432,malignant neoplasm of acoustic nerve,
+BMGC_DS06061,BMG_DS018090,,,,,,,DOID:4870,lacrimal gland adenoid cystic carcinoma,C0346340,,,MONDO:0006262,lacrimal gland adenoid cystic carcinoma,
+BMGC_DS06062,BMG_DS018091,,,,,,,DOID:298,lacrimal gland adenocarcinoma,C0346341,,,MONDO:0002475,lacrimal gland adenocarcinoma,
+BMGC_DS06063,BMG_DS018092,,,,,,,DOID:296,mixed lacrimal gland cancer,C0346342,,,MONDO:0002469,lacrimal gland carcinoma ex pleomorphic adenoma,
+BMGC_DS06064,BMG_DS018093,,,,,,,DOID:3259,orbit rhabdomyosarcoma,C0346347,,,MONDO:0002580,orbit rhabdomyosarcoma,
+BMGC_DS06065,BMG_DS018094,,,,,,,DOID:14463,cavernous hemangioma of orbit,C0346352,,,MONDO:0001975,cavernous hemangioma of orbit,
+BMGC_DS06066,BMG_DS018095,,,,,,,DOID:1748,conjunctival squamous cell carcinoma,C0346359,,,MONDO:0006173,conjunctival squamous cell carcinoma,
+BMGC_DS06067,BMG_DS018096,,,,,,,DOID:1751,malignant conjunctival melanoma,C0346360,,,MONDO:0002096,malignant conjunctival melanoma,
+BMGC_DS06068,BMG_DS018098,,,,,,,DOID:13538,cornea squamous cell carcinoma,C0346366,,,MONDO:0001740,cornea squamous cell carcinoma,
+BMGC_DS06069,BMG_DS018099,,,,,,,DOID:8400,malignant cornea melanoma,C0346367,,,MONDO:0004550,malignant cornea melanoma,
+BMGC_DS06070,BMG_DS018100,,,,,,,DOID:3478,iris cancer,C0346372,,,MONDO:0002658,iris cancer,
+BMGC_DS06071,BMG_DS018101,,,,,,,DOID:6994,malignant iris melanoma,C0346373,,,MONDO:0004064,iris melanoma,
+BMGC_DS06072,BMG_DS018103,,,,,,,DOID:6524,malignant ciliary body melanoma,C0346379,,,MONDO:0003912,malignant ciliary body melanoma,
+BMGC_DS06073,BMG_DS018105,,,,,,,DOID:6438,malignant choroid melanoma,C0346388,,,MONDO:0003878,malignant choroid melanoma,
+BMGC_DS06074,BMG_DS018107,,,,,,,DOID:660,adrenal cortex cancer,C0346402,,,MONDO:0021312,malignant tumor of adrenal cortex,
+BMGC_DS06075,BMG_DS018110,,,,,,,,,C0346421,,,MONDO:0015687,chronic eosinophilic leukemia,
+BMGC_DS06076,BMG_DS018111,,,,,,,DOID:265,spleen angiosarcoma,C0346424,,,MONDO:0002376,spleen angiosarcoma,
+BMGC_DS06077,BMG_DS018113,,,,,,,DOID:7696,lung hilum cancer,C0346601,,,,,
+BMGC_DS06078,BMG_DS018114,,,,,,,DOID:116,pericardium cancer,C0346609,,,MONDO:0001322,pericardium cancer,
+BMGC_DS06079,BMG_DS018115,,,,,,,DOID:4699,epicardium cancer,C0346610,,,,,
+BMGC_DS06080,BMG_DS018116,,,,,,,DOID:9299,myocardium cancer,C0346611,,,MONDO:0004749,myocardium cancer,
+BMGC_DS06081,BMG_DS018117,,,,,,,DOID:5877,endocardium cancer,C0346612,,,MONDO:0003687,endocardium cancer,
+BMGC_DS06082,BMG_DS018118,,,,,,,,,C0346619,,,MONDO:0850129,gastroesophageal cancer,
+BMGC_DS06083,BMG_DS018119,,,,,,,DOID:10155,intestinal cancer,C0346627,,,MONDO:0005814,intestinal cancer,
+BMGC_DS06084,BMG_DS018120,,,,,,,DOID:9256;DOID:5672,colorectal cancer | large intestine cancer,C0346629,,114500,MONDO:0005575,colorectal cancer,
+BMGC_DS06085,BMG_DS018121,,,,,,,DOID:1795,malignant exocrine pancreas neoplasm,C0346648,,,MONDO:0002116,malignant exocrine pancreas neoplasm,
+BMGC_DS06086,BMG_DS018122,,,,,,,DOID:4364,malignant breast melanoma,C0346787,,,MONDO:0002975,malignant breast melanoma,
+BMGC_DS06087,BMG_DS018123,,,,,,,DOID:5274,malignant dermis tumor,C0346811,,,MONDO:0003363,malignant dermis tumor,
+BMGC_DS06088,BMG_DS018124,,,,,,,DOID:175,vascular cancer,C0346845,,,,,
+BMGC_DS06089,BMG_DS018125,,,,,,,DOID:10744,broad ligament malignant neoplasm,C0346866,,,MONDO:0001108,broad ligament malignant neoplasm,
+BMGC_DS06090,BMG_DS018126,,,,,,,DOID:11748,round ligament malignant neoplasm,C0346867,,,MONDO:0001352,round ligament malignant neoplasm,
+BMGC_DS06091,BMG_DS018127,,,,,,,DOID:6098,thalamic neoplasm,C0346902,,,MONDO:0003766,thalamic cancer,
+BMGC_DS06092,BMG_DS018129,,,,,,,DOID:3541,cerebral ventricle cancer,C0346906,,,,,
+BMGC_DS06093,BMG_DS018130,,,,,,,DOID:8632,Kaposi's sarcoma,C0346935,,,,,
+BMGC_DS06094,BMG_DS018131,,,,,,,DOID:8632,Kaposi's sarcoma,C0346936,,,,,
+BMGC_DS06095,BMG_DS018132,,,,,,,DOID:6758,chest wall lymphoma,C0346948,,,MONDO:0021323,malignant neoplasm of chest wall,
+BMGC_DS06096,BMG_DS018133,,,,,,,,,C0346974,,,MONDO:0041447,metastatic malignant neoplasm in the colon,
+BMGC_DS06097,BMG_DS018138,,,,,,,DOID:6148,nasal cavity carcinoma in situ,C0347095,,,MONDO:0003784,nasal cavity carcinoma in situ,
+BMGC_DS06098,BMG_DS018146,,,,,,,DOID:8687,skin carcinoma in situ,C0347139,,,,,
+BMGC_DS06099,BMG_DS018153,,,,,,,DOID:9310,nasal cavity benign neoplasm,C0347215,,,MONDO:0021475,benign neoplasm of nasal cavity,
+BMGC_DS06100,BMG_DS018160,,,,,,,,,C0347272,,,MONDO:0021444,benign neoplasm of large intestine,
+BMGC_DS06101,BMG_DS018166,,,,,,,DOID:3178,skin papilloma,C0347390,,,MONDO:0002536,skin papilloma,
+BMGC_DS06102,BMG_DS018167,,,,,,,DOID:10188,skin lipoma,C0347394,,,MONDO:0000964,skin lipoma,
+BMGC_DS06103,BMG_DS018172,,,,,,,DOID:13743,spinal cord lipoma,C0347446,,,MONDO:0001790,spinal cord lipoma,
+BMGC_DS06104,BMG_DS018177,,,,,,,DOID:1138,spinal meningioma,C0347515,,,MONDO:0001275,spinal meningioma,
+BMGC_DS06105,BMG_DS018194,,"Epilepsy, Akinetic","Epilepsy, Generalized",,,,,,C0347869,D004829,,,,
+BMGC_DS06106,BMG_DS018223,205808005,Congenital malformation syndromes associated with short stature,,,,,,,C0347915,,,,,Congenital malformation syndromes associated with short stature | Congenital malformation syndromes associated with short stature (disorder)
+BMGC_DS06107,BMG_DS018225,,Non-Syphilitic Argyll-Robertson Pupil,Pupil Disorders,,,,,,C0347925,D011681,,,,
+BMGC_DS06108,BMG_DS018229,155578006;155579003;266398009;266364000;708038006;195981004,Asthma attack,,,,,,,C0347950,,,,,Asthma attack (& NOS) | Asthma attack NOS | Asthma attack | Asthma attack (& NOS) (disorder) | Asthma attack | Asthma NOS | Asthma: [NOS] or [attack] | Asthma: [NOS] or [attack] (disorder) | Asthma attack | Asthma attack (disorder) | Asthma attack | Acute exacerbation of asthma | Acute exacerbation of asthma (disorder) | Asthma attack NOS | Asthma attack | Asthma attack (& NOS) | Asthma attack (& NOS) (disorder)
+BMGC_DS06109,BMG_DS018352,,,,,,,DOID:1325,bronchus cancer,C0348343,,,,,
+BMGC_DS06110,BMG_DS018353,,,,,,,DOID:3996,urinary system cancer,C0348371,,,,,
+BMGC_DS06111,BMG_DS018354,,,,,,,DOID:3620,central nervous system cancer,C0348374,,,MONDO:0002714,central nervous system cancer,
+BMGC_DS06112,BMG_DS018363,,Other hypoparathyroidism,,5A50.Z,"Hypoparathyroidism, unspecified",E20.8,DOID:0090109,autosomal dominant hypocalcemia,C0348454,,,,,
+BMGC_DS06113,BMG_DS018365,,Other disorders of pituitary gland,,5A6Z,"Disorders of the pituitary hormone system, unspecified",E23.6,DOID:0090088,hypogonadotropic hypogonadism 24 without anosmia,C0348457,,,,,
+BMGC_DS06114,BMG_DS018368,,Other hyperaldosteronism,,5A72.Z,"Hyperaldosteronism, unspecified",E26.8;E26.89,DOID:0110143;DOID:0110147;DOID:0110142;DOID:0110145;DOID:0110146;DOID:0110144,Bartter disease type 2 | Bartter disease type 1 | Bartter disease type 3 | Bartter disease type 4b | Bartter disease type 4a | Bartter disease type 5,C0348460,,,,,
+BMGC_DS06115,BMG_DS018379,,Other disorders of branched-chain amino-acid metabolism,,5C50.DZ,"Disorders of branchedchain amino acid metabolism, unspecified",E71.19;E71.1,DOID:0090126;DOID:0060742;DOID:0060741;DOID:0060743,methylmalonic acidemia cblB type | methylmalonic acidemia cblA type | methylmalonic acidemia due to transcobalamin receptor defect | branched-chain keto acid dehydrogenase kinase deficiency,C0348484,,,,,
+BMGC_DS06116,BMG_DS018384,,Other sphingolipidosis,,5D2Z,"Metabolic disorders, unspecified",E75.2;E75.29,DOID:0070112;DOID:0110958;DOID:0070114;DOID:0090111;DOID:0070113;DOID:0110961;DOID:0060789;DOID:0060787;DOID:0060798;DOID:0110957;DOID:0110960;DOID:0110959;DOID:0070111;DOID:0060791;DOID:0060790;DOID:0060868,leukoencephalopathy with vanishing white matter | hypomyelinating leukodystrophy 6 | hypomyelinating leukodystrophy 9 | Niemann-Pick disease type A | hypomyelinating leukodystrophy 4 | Gaucher's disease perinatal lethal | atypical Gaucher's disease due to saposin c deficiency | Niemann-Pick disease type C1 | Niemann-Pick disease type C2 | hypomyelinating leukodystrophy 3 | PCWH syndrome | Niemann-Pick disease type B | Gaucher's disease type III | Gaucher's disease type I | hypomyelinating leukodystrophy 2 | Gaucher's disease type II,C0348489,,,,,
+BMGC_DS06117,BMG_DS018443,,Other cardiomyopathies,,BC43.Y,Other specified cardiomyopathy,I42.8,DOID:0110082;DOID:0110072;DOID:0110077;DOID:0110081;DOID:0110083;DOID:0110074;DOID:0110084;DOID:0110076;DOID:0110073;DOID:0110075,arrhythmogenic right ventricular dysplasia 10 | arrhythmogenic right ventricular dysplasia 6 | arrhythmogenic right ventricular dysplasia 9 | arrhythmogenic right ventricular dysplasia 11 | arrhythmogenic right ventricular dysplasia 5 | arrhythmogenic right ventricular dysplasia 4 | arrhythmogenic right ventricular dysplasia 3 | arrhythmogenic right ventricular dysplasia 12 | arrhythmogenic right ventricular dysplasia 13 | arrhythmogenic right ventricular dysplasia 8,C0348617,,,,,
+BMGC_DS06118,BMG_DS018446,,Other specified cardiac arrhythmias,,BE2Y,Other specified diseases of the circulatory system,I49.8,DOID:0110218;DOID:0110226,Brugada syndrome 1 | Brugada syndrome 9,C0348626,,,,,
+BMGC_DS06119,BMG_DS018518,,Other specified diseases of liver,,DB9Z,"Diseases of liver, unspecified",K76.8;K76.89,DOID:0050674,congenital bile acid synthesis defect,C0348751,,,,,
+BMGC_DS06120,BMG_DS018582,186318004,Listerial endocarditis,,,,A32.82,,,C0348868,,,,,Listerial endocarditis | Listerial endocarditis (disorder)
+BMGC_DS06121,BMG_DS018590,,"Aplastic anemia, idiopathic",,,,,,,C0348890,C538494,609135,MONDO:0012197,idiopathic aplastic anemia,
+BMGC_DS06122,BMG_DS018595,197125005,Irritable bowel syndrome with diarrhea,,,,K58.0,,,C0348898,,,,,Irritable bowel syndrome with diarrhoea | Irritable bowel syndrome with diarrhea | Irritable bowel syndrome with diarrhea (disorder)
+BMGC_DS06123,BMG_DS018617,190425002,Other specified diabetes mellitus with unspecified complications,,5A13,"Diabetes mellitus, other specified type",E13.8,DOID:0110629,Wolfram syndrome 1,C0348932,,,,,Other specified diabetes mellitus with unspecified complications | Other specified diabetes mellitus with unspecified complications (disorder)
+BMGC_DS06124,BMG_DS018663,,Cerebral Cryptococcosis,"Meningitis, Cryptococcal",,,,DOID:0080159,Cryptococcal meningitis,C0348991,D016919,,,,
+BMGC_DS06125,BMG_DS018683,,,,,,,DOID:591,phobic disorder,C0349231,,,MONDO:0003699,phobic disorder,
+BMGC_DS06126,BMG_DS018684,,Nonorganic Insomnia,Sleep Initiation and Maintenance Disorders,,,,,,C0349255,D007319,,,,
+BMGC_DS06127,BMG_DS018713,,,,,,,DOID:10915,Wernicke-Korsakoff syndrome,C0349464,,277730,MONDO:0010198,Wernicke-Korsakoff syndrome,
+BMGC_DS06128,BMG_DS018726,,Fetal Hypoxia,Fetal Hypoxia,,,,,,C0349489,D005311,,,,
+BMGC_DS06129,BMG_DS018736,,,,,,,DOID:13691,dermoid cyst of skin,C0349502,,,MONDO:0001778,dermoid cyst of skin,
+BMGC_DS06130,BMG_DS018737,,,,,,,,,C0349506,,,MONDO:0005434,skin sensitivity to sun,
+BMGC_DS06131,BMG_DS018740,,,,,,,DOID:10054,skin amelanotic melanoma,C0349515,,,MONDO:0005208,amelanotic skin melanoma,
+BMGC_DS06132,BMG_DS018750,,,,,,,DOID:10541,microinvasive gastric cancer,C0349530,,,MONDO:0001060,microinvasive gastric cancer,
+BMGC_DS06133,BMG_DS018751,,,,,,,DOID:10540,gastric lymphoma,C0349532,,,MONDO:0001059,gastric lymphoma,
+BMGC_DS06134,BMG_DS018752,,,,,,,DOID:4284,anal margin carcinoma,C0349534,,,MONDO:0002941,anal margin carcinoma,
+BMGC_DS06135,BMG_DS018753,,,,,,,,,C0349535,,114900,MONDO:0021533,intestinal neuroendocrine tumor G1,
+BMGC_DS06136,BMG_DS018755,,,,,,,DOID:14145,malignant anus melanoma,C0349538,,,MONDO:0006081,anal melanoma,
+BMGC_DS06137,BMG_DS018756,,,,,,,DOID:1992,rectum malignant melanoma,C0349539,,,MONDO:0002167,rectum malignant melanoma,
+BMGC_DS06138,BMG_DS018757,,,,,,,DOID:4863,spinal cord astrocytoma,C0349540,,,MONDO:0003174,spinal cord astrocytoma,
+BMGC_DS06139,BMG_DS018758,,,,,,,DOID:3073,brain glioblastoma multiforme,C0349543,,,MONDO:0002501,brain glioblastoma,
+BMGC_DS06140,BMG_DS018759,,,,,,,DOID:13159,scrotum squamous cell carcinoma,C0349551,,,MONDO:0001651,scrotum squamous cell carcinoma,
+BMGC_DS06141,BMG_DS018761,,,,,,,DOID:2025,gestational choriocarcinoma,C0349557,,,MONDO:0020550,gestational choriocarcinoma,
+BMGC_DS06142,BMG_DS018762,,,,,,,DOID:3999,Bartholin's gland carcinoma,C0349561,,,MONDO:0002829,bartholin gland carcinoma,
+BMGC_DS06143,BMG_DS018765,,,,,,,DOID:0050865,tongue squamous cell carcinoma,C0349566,,,MONDO:0000500,tongue squamous cell carcinoma,
+BMGC_DS06144,BMG_DS018766,,,,,,,DOID:116,pericardium cancer,C0349574,,,MONDO:0021381,neoplasm of pericardium,
+BMGC_DS06145,BMG_DS018768,,,,,,,DOID:5665,external ear cancer,C0349576,,,MONDO:0003574,external ear cancer,
+BMGC_DS06146,BMG_DS018769,,Complex Endometrial Hyperplasia,Endometrial Hyperplasia,,,,DOID:0080365,endometrial hyperplasia,C0349578,D004714,,MONDO:0041161;MONDO:0006169,complex endometrial hyperplasia | obsolete endometrial hyperplasia,
+BMGC_DS06147,BMG_DS018770,,Atypical Endometrial Hyperplasia,Endometrial Hyperplasia,,,,DOID:0080365,endometrial hyperplasia,C0349579,D004714,,MONDO:0006096;MONDO:0041161,atypical endometrial hyperplasia | obsolete endometrial hyperplasia,
+BMGC_DS06148,BMG_DS018771,,,,,,,DOID:3202,neurilemmoma of the fifth cranial nerve,C0349582,,,MONDO:0002555,trigeminal schwannoma,
+BMGC_DS06149,BMG_DS018775,,,,,,,DOID:0080842,intracranial meningioma,C0349604,,,MONDO:0850302,intracranial meningioma,
+BMGC_DS06150,BMG_DS018776,,Central Nervous System Cysts,Central Nervous System Cysts,,,,,,C0349606,D020863,,MONDO:0005262,central nervous system cyst,
+BMGC_DS06151,BMG_DS018781,,,,,,,DOID:4853,pilocytic astrocytoma of cerebellum,C0349620,,,MONDO:0003168,cerebellar pilocytic astrocytoma,
+BMGC_DS06152,BMG_DS018782,,,,,,,DOID:1660,malignant pineal area germ cell neoplasm,C0349621,,,,,
+BMGC_DS06153,BMG_DS018783,,,,,,,DOID:4957,meninges hemangiopericytoma,C0349622,,,MONDO:0003223,meninges hemangiopericytoma,
+BMGC_DS06154,BMG_DS018784,,,,,,,DOID:4955,central nervous system melanocytic neoplasm,C0349623,,,,,
+BMGC_DS06155,BMG_DS018787,,,,,,,DOID:1703,Richter's syndrome,C0349631,,,MONDO:0002083,Richter syndrome,
+BMGC_DS06156,BMG_DS018789,,,,,,,DOID:713,HCL-V,C0349633,,,MONDO:0017600,hairy cell leukemia variant,
+BMGC_DS06157,BMG_DS018790,,,,,,,,,C0349636,,,MONDO:0020511,precursor B-cell acute lymphoblastic leukemia,
+BMGC_DS06158,BMG_DS018791,,,,,,,DOID:0050458,juvenile myelomonocytic leukemia,C0349639,,607785,MONDO:0011908,juvenile myelomonocytic leukemia,
+BMGC_DS06159,BMG_DS018794,,,,,,,DOID:12253,testicular lymphoma,C0349644,,,MONDO:0001472,testicular lymphoma,
+BMGC_DS06160,BMG_DS018795,,,,,,,DOID:3319,lymphangioleiomyomatosis,C0349649,,,MONDO:0006277,lung lymphangioleiomyomatosis,
+BMGC_DS06161,BMG_DS018796,277869007,Non-tuberculous mycobacterial pneumonia,,,,,,,C0349650,,,,,Non-tuberculous mycobacterial pneumonia | Non-tuberculous mycobacterial pneumonia (disorder)
+BMGC_DS06162,BMG_DS018797,,Congenital disorder of glycosylation type 1A,,,,,,,C0349653,C535739,212065,MONDO:0008907,PMM2-congenital disorder of glycosylation,
+BMGC_DS06163,BMG_DS018798,,"Congenital Disorder Of Glycosylation, Type I-IIX",,,,,,,C0349655,C562844,212067,MONDO:0008909,"congenital disorder of glycosylation, type i/IIx",
+BMGC_DS06164,BMG_DS018799,,,,,,,DOID:5536,sarcomatoid squamous cell skin carcinoma,C0349656,,,MONDO:0003499,sarcomatoid squamous cell skin carcinoma,
+BMGC_DS06165,BMG_DS018800,,,,,,,DOID:3751,plantar verrucous skin carcinoma,C0349657,,,MONDO:0002765,plantar verrucous skin carcinoma,
+BMGC_DS06166,BMG_DS018805,,,,,,,DOID:11812,bladder sarcoma,C0349666,,,MONDO:0001374,bladder sarcoma,
+BMGC_DS06167,BMG_DS018806,,,,,,,DOID:3017,breast sarcoma,C0349667,,,MONDO:0002490,breast sarcoma,
+BMGC_DS06168,BMG_DS018807,,,,,,,DOID:5826,breast lymphoma,C0349669,,,,,
+BMGC_DS06169,BMG_DS018820,,Hypoglossal Neuralgia,Hypoglossal Nerve Diseases,,,,,,C0349716,D020437,,,,
+BMGC_DS06170,BMG_DS018821,240475000,Herpes simplex infection of skin,,,,,,,C0349719,,,,,Scrum pox | Cutaneous herpes simplex infection | Herpes simplex infection of skin | Herpes simplex infection of skin (disorder)
+BMGC_DS06171,BMG_DS018825,280486004,Female pelvic cellulitis,,,,,,,C0349734,,,,,Female pelvic cellulitis | Female pelvic cellulitis (disorder)
+BMGC_DS06172,BMG_DS018839,271366000,Diverticulitis of gastrointestinal tract,,,,,,,C0349774,,,,,Diverticulitis of gastrointestinal tract | Diverticulitis of gastrointestinal tract (disorder)
+BMGC_DS06173,BMG_DS018843,,Arrhythmogenic Right Ventricular Dysplasia,Arrhythmogenic Right Ventricular Dysplasia,,,,DOID:0050431,arrhythmogenic right ventricular cardiomyopathy,C0349788,D019571,,MONDO:0016587,arrhythmogenic right ventricular cardiomyopathy,
+BMGC_DS06174,BMG_DS018844,,,,,,,,,C0349790,,,MONDO:0850283,acute asthma,
+BMGC_DS06175,BMG_DS018850,,,,,,,DOID:11716,prediabetes syndrome,C0362046,,,MONDO:0006920,prediabetes syndrome,
+BMGC_DS06176,BMG_DS018854,,,,,,,DOID:1245,vulva cancer,C0375071,,,MONDO:0001528,vulva cancer,
+BMGC_DS06177,BMG_DS018856,,,,,,,DOID:14559,anaerobic meningitis,C0375197,,,,,
+BMGC_DS06178,BMG_DS018857,446995005,Shuddering attacks,,,,,DOID:1713,benign shuddering attacks,C0375200,,,MONDO:0002085,benign shuddering attacks,Shuddering attacks (disorder) | Benign shuddering attacks | Shuddering attacks
+BMGC_DS06179,BMG_DS018863,91357005,Acute endocarditis,,,,,DOID:10314,endocarditis,C0375268,,,,,Acute endocarditis | Acute endocarditis (disorder)
+BMGC_DS06180,BMG_DS018864,,,,,,,DOID:807,carotid artery occlusion,C0375275,,,,,
+BMGC_DS06181,BMG_DS018867,,Pneumonia due to other streptococci,,CA40.0Y,Pneumonia due to other specified bacteria,J15.4,,,C0375326,,,,,
+BMGC_DS06182,BMG_DS018868,,,,,,,DOID:873,anaerobic pneumonia,C0375327,,,,,
+BMGC_DS06183,BMG_DS018872,441971007,Chronic left-sided ulcerative colitis,,,,,DOID:8577,ulcerative colitis,C0375359,,,,,Chronic left-sided ulcerative colitis | Chronic left-sided ulcerative colitis (disorder)
+BMGC_DS06184,BMG_DS018879,16031000119101,Urethral intrinsic sphincter deficiency,,,,,DOID:13461,urethral intrinsic sphincter deficiency,C0375381,,,MONDO:0001721,urethral intrinsic sphincter deficiency,Urethral intrinsic sphincter deficiency | Urethral intrinsic sphincter deficiency (finding)
+BMGC_DS06185,BMG_DS018881,,,,,,,DOID:10123,pigmentation disease,C0375489,,,,,
+BMGC_DS06186,BMG_DS018883,,,,,,,DOID:11685,inflamed seborrheic keratosis,C0376117,,,MONDO:0001337,inflamed seborrheic keratosis,
+BMGC_DS06187,BMG_DS018884,,Necrotizing Hemorrhagic Encephalomyelitis,"Leukoencephalitis, Acute Hemorrhagic",,,,,,C0376171,D004684,,,,
+BMGC_DS06188,BMG_DS018885,,Bell Palsy,Bell Palsy,,,,DOID:12506,Bell's palsy,C0376175,D020330,,MONDO:0005665,Bell's palsy,
+BMGC_DS06189,BMG_DS018886,,"Hypoaldosteronism, Hyporeninemic",Hypoaldosteronism,,,,,,C0376185,D006994,,MONDO:0100161,hyperkalemic renal tubular acidosis,
+BMGC_DS06190,BMG_DS018888,154729006;85670002;267494000,Avitaminosis,Avitaminosis,,,,,,C0376286,D001361,,,,(Other vitamin deficiency) or (avitaminosis) | Other vitamin deficiency | Avitaminosis | (Other vitamin deficiency) or (avitaminosis) (disorder) | Vitamin deficiency | Hypovitaminosis | Avitaminosis | Vitamin deficiency (disorder) | Avitaminosis | Other vitamin deficiency | (Other vitamin deficiency) or (avitaminosis) | (Other vitamin deficiency) or (avitaminosis) (disorder)
+BMGC_DS06191,BMG_DS018889,70449006,Amaurosis,Blindness,,,,,,C0376288,D001766,MTHU023011,,,Amaurosis | Amaurosis (disorder)
+BMGC_DS06192,BMG_DS018890,,Dengue Shock Syndrome,Severe Dengue,,,,,,C0376300,D019595,,MONDO:0000248,dengue shock syndrome,
+BMGC_DS06193,BMG_DS018892,,,,,,,DOID:7280,congenital epulis,C0376319,,,MONDO:0015528,congenital epulis,
+BMGC_DS06194,BMG_DS018893,,Congestive Ophthalmopathy,Graves Ophthalmopathy,,,,DOID:0081120,Graves ophthalmopathy,C0376323,D049970,,,,
+BMGC_DS06195,BMG_DS018894,,New Variant Creutzfeldt-Jakob Disease,Creutzfeldt-Jakob Syndrome,,,,,,C0376329,D007562,,MONDO:0007012,variant Creutzfeldt-Jakob disease,
+BMGC_DS06196,BMG_DS018895,,Premenstrual Tension,Premenstrual Syndrome,,,,DOID:727,premenstrual tension,C0376356,D011293,,MONDO:0004169,premenstrual tension,
+BMGC_DS06197,BMG_DS018896,,,,,,,DOID:10283,prostate cancer,C0376358,,,MONDO:0008315,prostate cancer,
+BMGC_DS06198,BMG_DS018897,,Gronblad-Strandberg Syndrome,Pseudoxanthoma Elasticum,,,,,,C0376359,D011561,,,,
+BMGC_DS06199,BMG_DS018898,,Purpura Hemorrhagica,IgA Vasculitis,,,,,,C0376362,D011695,,,,
+BMGC_DS06200,BMG_DS018899,,Posterior Cervical Sympathetic Syndrome,Posterior Cervical Sympathetic Syndrome,,,,DOID:6692,Barre-Lieou syndrome,C0376378,D055010,,MONDO:0005663,Barre-Lieou syndrome,
+BMGC_DS06201,BMG_DS018902,,"Hibernation, Myocardial",Myocardial Stunning,,,,,,C0376416,D017682,,,,
+BMGC_DS06202,BMG_DS018903,,,,,,,DOID:3086,gingival overgrowth,C0376480,,,MONDO:0002507,gingival overgrowth,
+BMGC_DS06203,BMG_DS018904,,Branchio-Oculo-Facial Syndrome,Branchio-Oto-Renal Syndrome,,,,,,C0376524,D019280,113620,MONDO:0007235,branchiooculofacial syndrome,
+BMGC_DS06204,BMG_DS018905,,,,,,,DOID:3842,skull base cancer,C0376527,,,MONDO:0002785,skull base neoplasm,
+BMGC_DS06205,BMG_DS018906,,"Epilepsy, Rolandic","Epilepsy, Rolandic",,,,DOID:3329,benign epilepsy with centrotemporal spikes,C0376532,D019305,117100,MONDO:0007295,childhood epilepsy with centrotemporal spikes,
+BMGC_DS06206,BMG_DS018908,,,,,,,DOID:2531,hematologic cancer,C0376544,,,MONDO:0044881,hematopoietic and lymphoid cell neoplasm,
+BMGC_DS06207,BMG_DS018912,371770009;82042006,Endotoxemia,Endotoxemia,,,,,,C0376618,D019446,,,,Endotoxemia (disorder) | Endotoxaemia | Endotoxemia | Endotoxic shock | Gram-negative shock | Gram-negative septic shock | Endotoxemia | Endotoxaemia | Endotoxic shock (disorder)
+BMGC_DS06208,BMG_DS018914,,"Pancreatitis, Alcoholic","Pancreatitis, Alcoholic",,,,DOID:4988,alcoholic pancreatitis,C0376670,D019512,,MONDO:0003232,alcoholic pancreatitis,
+BMGC_DS06209,BMG_DS018915,,Shoulder Impingement Syndrome,Shoulder Impingement Syndrome,,,,DOID:14276,shoulder impingement syndrome,C0376685,D019534,,MONDO:0006968,shoulder impingement syndrome,
+BMGC_DS06210,BMG_DS018918,,Clinical Capillary Leak Syndrome,Capillary Leak Syndrome,,,,,,C0376704,D019559,,,,
+BMGC_DS06211,BMG_DS018919,,Esophageal Hernia,"Hernia, Hiatal",,,,DOID:12642,hiatus hernia,C0376710,D006551,,,,
+BMGC_DS06212,BMG_DS018921,,Tietz syndrome,,,,,DOID:0090002,Tietz syndrome,C0391816,C536919,103500,MONDO:0007077,Tietz syndrome,
+BMGC_DS06213,BMG_DS018926,,,,,,,DOID:6457,Cowden syndrome,C0391826,,,MONDO:0019002,Lhermitte-Duclos disease,
+BMGC_DS06214,BMG_DS018929,,,,,,,DOID:2839,erythropoietin polycythemia,C0391869,,,MONDO:0002440,erythropoietin polycythemia,
+BMGC_DS06215,BMG_DS018933,,Cervical Sympathetic Dystrophy,Reflex Sympathetic Dystrophy,,,,,,C0391959,D012019,,,,
+BMGC_DS06216,BMG_DS018944,33793000,Infarction of testis,,,,,DOID:5104,testicular infarct,C0392041,,,MONDO:0003279,testicular infarct,Infarction of testis | Testicular infarct | Testicular infarction | Infarction of testis (disorder)
+BMGC_DS06217,BMG_DS018947,48573006,Suppurative lymphadenopathy,,,,,DOID:4639,suppurative lymphadenitis,C0392051,,,MONDO:0003069,suppurative lymphadenitis,Suppurative lymphadenopathy | Suppurative lymphadenitis | Suppurative lymphadenopathy (disorder)
+BMGC_DS06218,BMG_DS018953,75403004,Cardiac sarcoidosis,,,,,DOID:13405,cardiac sarcoidosis,C0392077,,,MONDO:0001707,cardiac sarcoidosis,Cardiac sarcoidosis | Cardiac sarcoidosis (disorder)
+BMGC_DS06219,BMG_DS018958,,,,,,,DOID:0060313,tracheomalacia,C0392109,,,,,
+BMGC_DS06220,BMG_DS018964,50792001,Corneal erosion,,,,,,,C0392163,,,,,Corneal erosion | Superficial ulcer of cornea | Corneal erosion (disorder)
+BMGC_DS06221,BMG_DS018965,,Pulmonary Cystic Fibrosis,Cystic Fibrosis,,,,,,C0392164,D003550,,,,
+BMGC_DS06222,BMG_DS018970,109257007,Mucositis following radiation therapy,,,,,,,C0392190,,,,,Mucositis following radiation therapy | Radiation-induced mucositis | Mucositis following radiation therapy (disorder) | Ulcerative mucositis due to radiation
+BMGC_DS06223,BMG_DS018974,,,,,,,DOID:1790,malignant mesothelioma,C0392400,,,,,
+BMGC_DS06224,BMG_DS018975,86142006;200902009,Benign pemphigus,,,,,,,C0392436,,,,,Pemphigoid | Pemphigoid (disorder) | Benign pemphigus | Benign pemphigus (disorder)
+BMGC_DS06225,BMG_DS018976,27520001;83839005,Acrodermatitis continua of Hallopeau,,,,,,,C0392439,,614204,MONDO:0013626,"psoriasis 14, pustular",Pustulosis palmaris et plantaris | Recalcitrant pustular eruption of palms and soles | PPP - Palmoplantar pustulosis | Chronic palmoplantar pustular psoriasis | Palmoplantar pustular psoriasis | Pustular acrodermatitis | Pustular psoriasis of palms and soles | Palmoplantar pustulosis | Pustular psoriasis of palms and soles (disorder) | Acrodermatitis continua of Hallopeau | Dermatitis repens | Acrodermatitis continua of Hallopeau (disorder) | Acropustulosis | Acrodermatitis perstans
+BMGC_DS06226,BMG_DS018979,,Necrobiosis Lipoidica Diabeticorum,Necrobiosis Lipoidica,,,,,,C0392445,D009335,,,,
+BMGC_DS06227,BMG_DS018987,195057009;17869006,Anomalous atrioventricular excitation,,BC63.Z,"Conduction disorders, unspecified",I45.6,DOID:384,Wolff-Parkinson-White syndrome,C0392470,,,,,Anomalous atrioventricular excitation | Anomalous atrioventricular excitation (disorder)
+BMGC_DS06228,BMG_DS018988,48718006,Roberts-SC phocomelia syndrome,,,,,DOID:5325,Roberts syndrome,C0392475,,268300;269000,MONDO:0100253,Roberts-SC phocomelia syndrome,Roberts-SC phocomelia syndrome | Pseudothalidomide syndrome | Hypomelia-hypotrichosis-facial hemangioma syndrome | Hypomelia-hypotrichosis-facial haemangioma syndrome | Roberts-SC phocomelia syndrome (disorder) | Hypomelia hypotrichosis facial haemangioma syndrome | Hypomelia hypotrichosis facial hemangioma syndrome | Robert's syndrome
+BMGC_DS06229,BMG_DS018989,718052004,Asymptomatic periapical periodontitis,,,,,DOID:11269,chronic apical periodontitis,C0392492,,,MONDO:0001251,chronic apical periodontitis,Asymptomatic periapical periodontitis (disorder) | Asymptomatic periapical periodontitis | Chronic apical periodontitis | CAP - chronic apical periodontitis | Chronic periapical periodontitis | Chronic periradicular periodontitis
+BMGC_DS06230,BMG_DS018990,6971002,Hypertrophy of tongue papillae,,DA03.4,Hypertrophy of tongue papillae,K14.3,DOID:13333,hypertrophy of tongue papillae,C0392494,,,MONDO:0001689,hypertrophy of tongue papillae,Hypertrophy of tongue papillae | Hypertrophy of tongue papillae (disorder)
+BMGC_DS06231,BMG_DS018996,35400008;86781004;190845003,Hereditary hemochromatosis,,,,E83.110,,,C0392514,,,MONDO:0006507,hereditary hemochromatosis,Hereditary hemochromatosis | Familial hemochromatosis | Hereditary haemochromatosis | Familial haemochromatosis | Hereditary hemochromatosis (disorder) | Hemochromatosis | Bronzed cirrhosis | Pigmentary cirrhosis of liver | von Recklinghausen-Appelbaum disease | Iron storage disease | Familial hemochromatosis | Hereditary hemochromatosis | Primary hemochromatosis | Idiopathic hemochromatosis | Familial haemochromatosis | Hereditary haemochromatosis | Idiopathic haemochromatosis | Primary haemochromatosis | Bronzed diabetes | von Recklinghausen-Applebaum disease | Haemochromatosis | Hemochromatosis (disorder) | Hereditary hemochromatosis | Hereditary haemochromatosis | Hereditary haemochromatosis (disorder)
+BMGC_DS06232,BMG_DS018998,95570007;266623004;155868000;56491003,Nephrolithiasis,Nephrolithiasis,,,,,,C0392525,D053040,MTHU007103,MONDO:0008171,nephrolithiasis,Kidney stone | Renal stone | Nephrolith | Renal calculus | Calculus of kidney | Nephrolithiasis | Kidney calculus | Kidney stone (disorder) | Kidney calculus (& [staghorn]) | Kidney calculus | Nephrolithiasis | Staghorn calculus | Kidney calculus (& [staghorn]) (disorder) | Staghorn calculus | Kidney calculus | Nephrolithiasis | Kidney calculus (& [staghorn]) | Kidney calculus (& [staghorn]) (disorder) | Nephrolithiasis | Nephrolithiasis (disorder)
+BMGC_DS06233,BMG_DS019001,,Cauda Equina Syndrome,Cauda Equina Syndrome,,,,DOID:11577,Cauda equina syndrome,C0392548,D000077684,,MONDO:0005693,cauda equina syndrome,
+BMGC_DS06234,BMG_DS019003,,"Hemiplegia, Infantile",Hemiplegia,,,,DOID:10969,hemiplegia,C0392550,D006429,,,,
+BMGC_DS06235,BMG_DS019004,193158000;128202008;65017003,Hereditary peripheral neuropathy,,,,,DOID:0050539,Charcot-Marie-Tooth disease type 2,C0392553,,,,,Hereditary motor and sensory neuropathy | CMT - Charcot-Marie-Tooth disease | HMSN - Hereditary motor and sensory neuropathy | Peroneal muscular atrophy | Hereditary peripheral neuropathy | HSMN - Hereditary sensory and motor neuropathy | Charcot-Marie-Tooth disease | Hereditary motor and sensory neuropathy (disorder) | Hereditary sensory-motor neuropathy | Hereditary sensory and motor neuropathy | Hereditary sensorimotor neuropathy | HSMN | HMSN | Hereditary motor and sensory neuropathy | Hereditary peripheral neuropathy | CMT - Charcot-Marie-Tooth disease | HSMN - Hereditary sensory and motor neuropathy | HMSN - Hereditary motor and sensory neuropathy | Charcot-Marie-Tooth disease | Peroneal muscular atrophy | Hereditary motor and sensory neuropathy (disorder) | Hereditary peripheral neuropathy | Hereditary peripheral neuropathy (disorder)
+BMGC_DS06236,BMG_DS019009,,Severe combined immunodeficiency due to adenosine deaminase deficiency,,,,D81.31,,,C0392607,C531816,,,,
+BMGC_DS06237,BMG_DS019023,88594005,Herpes simplex without mention of complication,,,,,,,C0392646,,,,,Herpes simplex | Herpes simplex infection | Herpes simplex viral infection | Herpes simplex (disorder) | Herpes simplex complex
+BMGC_DS06238,BMG_DS019024,14189004,Measles without mention of complication,,,,,,,C0392650,,,,,Measles | Rubeola | Morbilli | Measles (disorder)
+BMGC_DS06239,BMG_DS019028,,Angiostrongyliasis,,,,,DOID:0050256,angiostrongyliasis,C0392662,C536369,,MONDO:0019143,angiostrongyliasis,
+BMGC_DS06240,BMG_DS019036,,,,,,,,,C0392788,,,MONDO:0019472,extranodal nasal NK/T cell lymphoma,
+BMGC_DS06241,BMG_DS019037,,,,,,,DOID:6170,ovarian carcinosarcoma,C0392998,,,MONDO:0003792,ovarian carcinosarcoma,
+BMGC_DS06242,BMG_DS019064,230155003,Non-infective meningitis,,,,,,,C0393442,,,,,Non-infective meningitis | Non-infective meningitis (disorder)
+BMGC_DS06243,BMG_DS019099,,Rasmussen Syndrome,Encephalitis,,,,,,C0393484,D004660,,,,
+BMGC_DS06244,BMG_DS019118,,"Cerebellar Ataxia, Early Onset",Spinocerebellar Degenerations,,,,,,C0393519,D013132,,,,
+BMGC_DS06245,BMG_DS019123,,"Cerebellar Ataxia, Late Onset",Spinocerebellar Degenerations,,,,,,C0393524,D013132,,,,
+BMGC_DS06246,BMG_DS019124,230233000,Progressive cerebellar ataxia,,,,,,,C0393525,,MTHU001770,,,Progressive cerebellar ataxia | Progressive cerebellar ataxia (disorder)
+BMGC_DS06247,BMG_DS019135,,"Muscular Atrophy, Spinal, Type II",Spinal Muscular Atrophies of Childhood,,,,DOID:0050530,intermediate spinal muscular atrophy,C0393538,D014897,253550,MONDO:0009673,"spinal muscular atrophy, type II",
+BMGC_DS06248,BMG_DS019136,,Childhood Progressive Bulbar Palsy,"Bulbar Palsy, Progressive",,,,,,C0393540,D010244,,,,
+BMGC_DS06249,BMG_DS019137,,Distal Spinal Muscular Atrophy,"Muscular Atrophy, Spinal",,,,,,C0393541,D009134,,MONDO:0018894,distal hereditary motor neuropathy,
+BMGC_DS06250,BMG_DS019141,,Oculopharyngeal Spinal Muscular Atrophy,"Muscular Atrophy, Spinal",,,,,,C0393546,D009134,,,,
+BMGC_DS06251,BMG_DS019142,,Bulbospinal Neuronopathy,"Muscular Atrophy, Spinal",,,,,,C0393547,D009134,,MONDO:0016113,bulbospinal muscular atrophy,
+BMGC_DS06252,BMG_DS019145,230255008,Madras-type motor neurone disease,,,,,,,C0393551,,,MONDO:0015307,Madras motor neuron disease,Madras-type motor neurone disease | Madras-type motor neurone disease (disorder)
+BMGC_DS06253,BMG_DS019148,,Amyotrophic Lateral Sclerosis With Dementia,Amyotrophic Lateral Sclerosis,,,,,,C0393554,D000690,,,,
+BMGC_DS06254,BMG_DS019150,230261006,Complicated hereditary spastic paraplegia,,,,,,,C0393556,,,MONDO:0015150,complex hereditary spastic paraplegia,Complicated hereditary spastic paraplegia | Complicated hereditary spastic paraplegia (disorder)
+BMGC_DS06255,BMG_DS019152,230264003,Troyer syndrome,,,,,,,C0393559,C536858,275900,MONDO:0010156,Troyer syndrome,Troyer syndrome | Troyer syndrome (disorder)
+BMGC_DS06256,BMG_DS019153,,"Vascular Dementia, Acute Onset","Dementia, Vascular",,,,,,C0393560,D015140,,,,
+BMGC_DS06257,BMG_DS019154,,Subcortical Vascular Dementia,"Dementia, Vascular",,,,,,C0393561,D015140,,,,
+BMGC_DS06258,BMG_DS019160,,,,,,,DOID:4752,multiple system atrophy,C0393571,,,MONDO:0007803,multiple system atrophy,
+BMGC_DS06259,BMG_DS019162,,"Huntington Disease, Late Onset",Huntington Disease,,,,,,C0393574,D006816,,,,
+BMGC_DS06260,BMG_DS019164,66881004,Neuroacanthocytosis,Neuroacanthocytosis,,,,DOID:0050766;DOID:0050765,choreaacanthocytosis | neuroacanthocytosis,C0393576,D054546,200150,MONDO:0008695;MONDO:0016987,chorea-acanthocytosis | neuroacanthocytosis,Choreoacanthocytosis | Choreoacanthocytosis (disorder)
+BMGC_DS06261,BMG_DS019170,,Benign Hereditary Chorea,Chorea,,,,,,C0393584,D002819,118700,MONDO:0021011,hereditary progressive chorea without dementia,
+BMGC_DS06262,BMG_DS019174,,,,,,,,,C0393588,,,MONDO:0016058,paroxysmal dystonia,
+BMGC_DS06263,BMG_DS019176,110997000,Fahr's syndrome (disorder),,,,,DOID:0060230,basal ganglia calcification,C0393590,,,,,Fahr's syndrome | Idiopathic nonarteriosclerotic cerebrovascular calcification | Cerebral symmetric calcification | Cerebrovascular ferrocalcinosis | Fahr's syndrome (disorder) | Fahr disease | Fahr syndrome
+BMGC_DS06264,BMG_DS019177,,Aicardi-Goutieres syndrome,,,,E79.81,,,C0393591,C535607,,MONDO:0018866,Aicardi-Goutieres syndrome,
+BMGC_DS06265,BMG_DS019179,,Dystonia Disorders,Dystonic Disorders,,,,DOID:543,dystonia,C0393593,D020821,,,,
+BMGC_DS06266,BMG_DS019182,230318005;192852006,Idiopathic familial dystonia,,8A02.0Z,"Primary dystonia, unspecified",G24.1,DOID:0050835;DOID:0090039;DOID:0090034;DOID:0060730;DOID:0090046;DOID:0090041;DOID:0090037;DOID:0090050;DOID:0090055;DOID:0090042;DOID:0090043;DOID:0090057;DOID:0090038,generalized dystonia | dystonia 27 | dystonia 21 | torsion dystonia 1 | dopa-responsive dystonia | torsion dystonia 2 | torsion dystonia 4 | torsion dystonia 13 | myoclonic dystonia 11 | dystonia 25 | X-linked dystonia-parkinsonism | torsion dystonia 6 | torsion dystonia 17,C0393598,,,MONDO:0044816,familial idiopathic torsion dystonia,Idiopathic familial dystonia | Idiopathic familial dystonia (disorder) | Genetic torsion dystonia | Idiopathic familial dystonia | Idiopathic familial dystonia (disorder)
+BMGC_DS06267,BMG_DS019185,230321007,Idiopathic non-familial dystonia,,,,,DOID:0050835,generalized dystonia,C0393601,,,MONDO:0044817,acquired idiopathic torsion dystonia,Idiopathic non-familial dystonia | Idiopathic non-familial dystonia (disorder)
+BMGC_DS06268,BMG_DS019196,,Familial Tremor,Essential Tremor,,,,,,C0393615,D020329,,,,
+BMGC_DS06269,BMG_DS019204,,Opsoclonus-Myoclonus Syndrome,Opsoclonus-Myoclonus Syndrome,,,,,,C0393626,D053578,,MONDO:0015247,opsoclonus-myoclonus syndrome,
+BMGC_DS06270,BMG_DS019213,,Hashimoto's encephalitis,,,,,,,C0393639,C535841,,MONDO:0019385,steroid-responsive encephalopathy associated with autoimmune thyroiditis,
+BMGC_DS06271,BMG_DS019232,,"Multiple Sclerosis, Acute Relapsing","Multiple Sclerosis, Relapsing-Remitting",,,,,,C0393664,D020529,,,,
+BMGC_DS06272,BMG_DS019233,,"Multiple Sclerosis, Chronic Progressive","Multiple Sclerosis, Chronic Progressive",,,,,,C0393665,D020528,,MONDO:0005284,chronic progressive multiple sclerosis,
+BMGC_DS06273,BMG_DS019234,,"Multiple Sclerosis, Progressive Relapsing","Multiple Sclerosis, Chronic Progressive",,,,DOID:0050785,progressive relapsing multiple sclerosis,C0393666,D020528,,MONDO:0000452,progressive relapsing multiple sclerosis,
+BMGC_DS06274,BMG_DS019235,,Extrapontine Myelinolysis,"Myelinolysis, Central Pontine",,,,,,C0393667,D017590,,,,
+BMGC_DS06275,BMG_DS019239,,"Frontal Epilepsy, Benign, Childhood","Epilepsy, Frontal Lobe",,,,,,C0393671,D017034,,,,
+BMGC_DS06276,BMG_DS019240,,"Epilepsy, Benign Psychomotor, Childhood","Epilepsy, Temporal Lobe",,,,,,C0393672,D004833,,,,
+BMGC_DS06277,BMG_DS019243,,Childhood Benign Occipital Epilepsy,"Epilepsies, Partial",,,,,,C0393675,D004828,,,,
+BMGC_DS06278,BMG_DS019244,,Panayiotopoulos Syndrome,"Epilepsies, Partial",,,,,,C0393676,D004828,,MONDO:0020307,self-limited epilepsy with autonomic seizures,
+BMGC_DS06279,BMG_DS019247,,Amygdalo-Hippocampal Epilepsy,"Epilepsies, Partial",,,,,,C0393679,D004828,,,,
+BMGC_DS06280,BMG_DS019249,,Rhinencephalic Epilepsy,"Epilepsies, Partial",,,,,,C0393681,D004828,,,,
+BMGC_DS06281,BMG_DS019250,,"Epilepsy, Lateral Temporal","Epilepsy, Temporal Lobe",,,,,,C0393682,D004833,,,,
+BMGC_DS06282,BMG_DS019251,,"Epilepsy, Supplementary Motor","Epilepsy, Frontal Lobe",,,,,,C0393683,D017034,,,,
+BMGC_DS06283,BMG_DS019252,,"Epilepsy, Cingulate","Epilepsy, Frontal Lobe",,,,,,C0393684,D017034,,,,
+BMGC_DS06284,BMG_DS019254,,"Epilepsy, Opercular","Epilepsy, Frontal Lobe",,,,,,C0393688,D017034,,,,
+BMGC_DS06285,BMG_DS019257,,Occipital Lobe Epilepsy,"Epilepsies, Partial",,,,,,C0393691,D004828,,,,
+BMGC_DS06286,BMG_DS019259,,"Benign Neonatal Epilepsy, Nonfamilial","Epilepsy, Benign Neonatal",,,,,,C0393693,D020936,,MONDO:0018981,benign idiopathic neonatal seizures,
+BMGC_DS06287,BMG_DS019260,,"Early Childhood Epilepsy, Myoclonic","Epilepsies, Myoclonic",,,,,,C0393695,D004831,,,,
+BMGC_DS06288,BMG_DS019262,,Cryptogenic Infantile Spasms,"Spasms, Infantile",,,,DOID:0050562,West syndrome,C0393698,D013036,,,,
+BMGC_DS06289,BMG_DS019263,,Symptomatic Infantile Spasms,"Spasms, Infantile",,,,DOID:0050562,West syndrome,C0393699,D013036,,,,
+BMGC_DS06290,BMG_DS019266,,Myoclonic Astatic Epilepsy,"Epilepsies, Myoclonic",,,,,,C0393702,D004831,,MONDO:0016025,myoclonic-astatic epilepsy,
+BMGC_DS06291,BMG_DS019267,,Myoclonic Absence Epilepsy,"Epilepsies, Myoclonic",,,,,,C0393703,D004831,,MONDO:0019487,epilepsy with myoclonic absences,
+BMGC_DS06292,BMG_DS019268,230429005,Early infantile epileptic encephalopathy with suppression bursts,,,,,,,C0393706,,,MONDO:0100062,developmental and epileptic encephalopathy,Early infantile epileptic encephalopathy with suppression bursts | Ohtahara syndrome | Early infantile epileptic encephalopathy with suppression bursts (disorder)
+BMGC_DS06293,BMG_DS019275,,"Reflex Epilepsy, Photosensitive","Epilepsy, Reflex",,,,,,C0393720,D020195,,MONDO:0015643,photosensitive epilepsy,
+BMGC_DS06294,BMG_DS019279,,,,,,,DOID:2550,tactile epilepsy,C0393724,,,MONDO:0002340,tactile epilepsy,
+BMGC_DS06295,BMG_DS019283,,Immersion Related Epilepsy,"Epilepsy, Reflex",,,,,,C0393729,D020195,,,,
+BMGC_DS06296,BMG_DS019286,,Complex Partial Status Epilepticus,Status Epilepticus,,,,,,C0393734,D013226,,,,
+BMGC_DS06297,BMG_DS019287,,Headache Disorders,Headache Disorders,,,,,,C0393735,D020773,,MONDO:0021146,headache disorder,
+BMGC_DS06298,BMG_DS019291,,Episodic Cluster Headache,Cluster Headache,,,,,,C0393739,D003027,,,,
+BMGC_DS06299,BMG_DS019295,,Atypical Cluster Headache,Cluster Headache,,,,,,C0393744,D003027,,,,
+BMGC_DS06300,BMG_DS019306,,Delayed Sleep Phase Syndrome,"Sleep Disorders, Circadian Rhythm",,,,,,C0393770,D020178,,MONDO:0024377,"circadian rhythm sleep disorder, delayed sleep phase type",
+BMGC_DS06301,BMG_DS019309,,Sleep-Related Bruxism,Sleep Bruxism,,,,DOID:2846,bruxism,C0393774,D020186,,,,
+BMGC_DS06302,BMG_DS019312,,,,,,,,,C0393778,,107200,MONDO:0007137,isolated congenital anosmia,
+BMGC_DS06303,BMG_DS019316,,"Trigeminal Neuralgia, Idiopathic",Trigeminal Neuralgia,,,,,,C0393786,D014277,,,,
+BMGC_DS06304,BMG_DS019317,,Secondary Trigeminal Neuralgia,Trigeminal Neuralgia,,,,,,C0393787,D014277,,,,
+BMGC_DS06305,BMG_DS019322,,Miller Fisher Syndrome,Miller Fisher Syndrome,8C01.0,Acute inflammatory demyelinating polyneuropathy,G61.0,DOID:12889,Miller Fisher syndrome,C0393799,D019846,,MONDO:0005851,Miller Fisher syndrome,
+BMGC_DS06306,BMG_DS019327,128203003,Hereditary motor and sensory neuropathy with optic atrophy (disorder),,,,,,,C0393807,,,MONDO:0019551,hereditary motor and sensory neuropathy type 6,"Hereditary sensory and motor neuropathy, type VI | Hereditary motor-sensory neuropathy, type VI | HMSN VI | Hereditary motor and sensory neuropathy with optic atrophy | Hereditary motor and sensory neuropathy with optic atrophy (disorder) | Hereditary motor and sensory neuropathy type VI | Hereditary motor-sensory neuropathy with optic atrophy"
+BMGC_DS06307,BMG_DS019328,,"Charcot-Marie-Tooth disease, X-linked, 1",,,,,,,C0393808,C535919,302800,MONDO:0010549,Charcot-Marie-Tooth disease X-linked dominant 1,
+BMGC_DS06308,BMG_DS019330,230558006,Hereditary liability to pressure palsies,,,,,DOID:0060843,hereditary neuropathy with liability to pressure palsies,C0393814,,162500,MONDO:0008087,hereditary neuropathy with liability to pressure palsies,Hereditary liability to pressure palsies | Tomaculous neuropathy | Hereditary liability to pressure palsies (disorder)
+BMGC_DS06309,BMG_DS019334,,"Polyradiculoneuropathy, Chronic Inflammatory Demyelinating","Polyradiculoneuropathy, Chronic Inflammatory Demyelinating",,,,DOID:5213;DOID:2536,chronic inflammatory demyelinating polyradiculoneuropathy | chronic inflammatory demyelinating polyneuritis,C0393819,D020277,,MONDO:0006702,chronic inflammatory demyelinating polyradiculoneuropathy,
+BMGC_DS06310,BMG_DS019350,,Diabetic Asymmetric Polyneuropathy,Diabetic Neuropathies,,,,,,C0393835,D003929,,,,
+BMGC_DS06311,BMG_DS019362,,"Polyneuropathy, Critical Illness",Polyneuropathies,,,,DOID:14402,critical illness polyneuropathy,C0393851,D011115,,MONDO:0001957,critical illness polyneuropathy,
+BMGC_DS06312,BMG_DS019399,,Segmental Autonomic Dysfunction,Autonomic Nervous System Diseases,,,,,,C0393912,D001342,,,,
+BMGC_DS06313,BMG_DS019411,230670003,Familial infantile myasthenia,,,,,,,C0393929,,254210,MONDO:0009689,congenital myasthenic syndrome 6,Familial infantile myasthenia | FIM - Familial infantile myasthenia | Familial infantile myasthenia (disorder)
+BMGC_DS06314,BMG_DS019420,,Neuromuscular Junction Toxic Disorders,Neuromuscular Junction Diseases,,,,,,C0393939,D020511,,,,
+BMGC_DS06315,BMG_DS019430,,Anterior Cerebral Circulation Infarction,Brain Infarction,,,,,,C0393953,D020520,,,,
+BMGC_DS06316,BMG_DS019457,,Multicystic Encephalomalacia,Encephalomalacia,,,,,,C0393992,D004678,,,,
+BMGC_DS06317,BMG_DS019465,,"Cerebral Palsy, Dystonic-Rigid",Cerebral Palsy,,,,,,C0394003,D002547,,,,
+BMGC_DS06318,BMG_DS019468,213341009;230782004,Dysequilibrium syndrome,,,,,DOID:0050997,"cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome",C0394006,,,MONDO:0009133,"cerebellar ataxia, intellectual disability, and dysequilibrium","Dysequilibrium syndrome | Dysequilibrium syndrome (disorder) | Dysequilibrium syndrome | Dysequilibrium syndrome (disorder) | Disequilibrium syndrome | DES - dysequilibrium syndrome | Non-progressive cerebellar ataxia, intellectual disability syndrome | Uner Tan syndrome | Cerebellar ataxia, intellectual disability, dysequilibrium syndrome | CAMRQ syndrome"
+BMGC_DS06319,BMG_DS019469,,"Cerebral Palsy, Atonic",Cerebral Palsy,,,,,,C0394007,D002547,,MONDO:0020695,hypotonic cerebral palsy,
+BMGC_DS06320,BMG_DS019474,,"Coma, Post-Head Injury","Coma, Post-Head Injury",,,,,,C0394016,D020207,,,,
+BMGC_DS06321,BMG_DS019477,,,,,,,,,C0395005,,,MONDO:0040871,psychogenic polydipsia,
+BMGC_DS06322,BMG_DS019493,232230009,Malignant otitis externa caused by Pseudomonas aeruginosa,,,,,,,C0395818,,,MONDO:0041095,malignant otitis externa caused by Pseudomonas aeruginosa,Malignant otitis externa caused by Pseudomonas aeruginosa | Malignant otitis externa caused by Pseudomonas aeruginosa (disorder)
+BMGC_DS06323,BMG_DS019512,204231005;301061006,Stenosis of external auditory canal,,,,,,,C0395837,,,,,(Stenosis of external auditory canal) or (congenital stricture: [external auditory canal] or [osseous meatus]) | Congenital stricture of osseous meatus | Congenital stricture of external auditory canal | Stenosis of external auditory canal | (Stenosis of external auditory canal) or (congenital stricture: [external auditory canal] or [osseous meatus]) (disorder) | Stenosis of external auditory canal | Stenosis of ear canal | Stenosis of external auditory canal (disorder)
+BMGC_DS06324,BMG_DS019515,89723004,Chronic tympanitis,,AB15,Chronic myringitis,H73.1,DOID:11217,chronic tympanitis,C0395849,,,MONDO:0001227,chronic tympanitis,Chronic tympanitis | Chronic myringitis | Chronic tympanitis (disorder)
+BMGC_DS06325,BMG_DS019520,52353000,Acute mucoid otitis media,,,,,DOID:9736,blue drum syndrome,C0395863,,,MONDO:0004865,blue drum syndrome,Acute mucoid otitis media | Blue drum syndrome | Acute mucoid otitis media (disorder) | Acute non-suppurative otitis media - mucoid
+BMGC_DS06326,BMG_DS019521,77478005,Acute sanguineous otitis media,,,,,DOID:3696,acute sanguinous otitis media,C0395865,,,MONDO:0002737,acute sanguinous otitis media,Acute sanguinous otitis media | Acute non-suppurative otitis media with haemotympanum | Acute non-suppurative otitis media with hemotympanum | Acute non-suppurative otitis media - sanguinous | Acute non-suppurative otitis media - bloody | Acute sanguineous otitis media (disorder) | Acute sanguineous otitis media
+BMGC_DS06327,BMG_DS019552,,Recurrent Vestibular Neuritis,Vestibular Neuronitis,,,,,,C0395932,D020338,,,,
+BMGC_DS06328,BMG_DS019558,,"Tinnitus, Noise Induced",Tinnitus,,,,,,C0395955,D014012,,,,
+BMGC_DS06329,BMG_DS019607,195794009;232420002,Chronic adenoiditis,,,,J35.02,DOID:0050145,adenoiditis,C0396023,,,,,Chronic adenoiditis | Chronic tonsillitis | (Chronic tonsillitis) or (chronic adenoiditis) | (Chronic tonsillitis) or (chronic adenoiditis) (disorder) | Chronic adenoiditis | Chronic adenoiditis (disorder)
+BMGC_DS06330,BMG_DS019628,253738002;232442001,Congenital laryngeal abductor palsy,,,,,,,C0396059,,150260,MONDO:0007876,laryngeal abductor paralysis,Congenital laryngeal abductor palsy | Congenital laryngeal abductor palsy (disorder) | Congenital laryngeal abductor palsy | Gerhardt syndrome | Congenital laryngeal abductor paralysis | Congenital laryngeal abductor palsy (disorder)
+BMGC_DS06331,BMG_DS019629,232443006;253739005,Congenital laryngeal adductor palsy,,,,,,,C0396060,,150270,MONDO:0007877,laryngeal adductor paralysis,Congenital laryngeal adductor paralysis | Congenital laryngeal adductor palsy | Congenital laryngeal adductor palsy (disorder) | Congenital laryngeal adductor palsy | Congenital laryngeal adductor palsy (disorder)
+BMGC_DS06332,BMG_DS019636,,,,,,,,,C0396072,,,MONDO:0023597,laryngeal papillomatosis,
+BMGC_DS06333,BMG_DS019642,31268005,Trousseau's syndrome,,,,,,,C0398359,,,,,Thrombophlebitis migrans | Trousseau's syndrome | Migratory thrombophlebitis | Thrombophlebitis migrans (disorder)
+BMGC_DS06334,BMG_DS019647,,,,,,,,,C0398368,,,MONDO:0019313,lymphatic malformation,
+BMGC_DS06335,BMG_DS019649,234102003,Lipedema,Lipedema,,,,,,C0398370,D065134,614103,MONDO:0013577,Lipedema,Lipedema | Lipoedema | Lipedema (disorder)
+BMGC_DS06336,BMG_DS019669,234405009,Triose phosphate isomerase deficiency,,,,,,,C0398562,,,,,Triose phosphate isomerase deficiency | TPI - Thiose phosphate isomerase deficiency | Triose phosphate isomerase deficiency (disorder) | Deficiency of phosphotriose isomerase | Deficiency of triosephosphate mutase
+BMGC_DS06337,BMG_DS019672,234411007,Blood group deletion syndrome,,,,,DOID:0112107,McLeod syndrome,C0398568,,300842,MONDO:0018945,McLeod neuroacanthocytosis syndrome,Blood group deletion syndrome | Blood group deletion syndrome (disorder) | McLeod syndrome
+BMGC_DS06338,BMG_DS019689,234431006,Specific granule deficiency,,,,,,,C0398593,,,MONDO:0009506,specific granule deficiency,Specific granule deficiency | SGD - Specific granule deficiency | Specific granule deficiency (disorder)
+BMGC_DS06339,BMG_DS019690,,Myeloperoxidase Deficiency,,,,,,,C0398595,C562864,254600,MONDO:0009694,myeloperoxidase deficiency,
+BMGC_DS06340,BMG_DS019708,95840007,Hypoplasminogenemia,,,,E88.02,DOID:0111592,plasminogen deficiency type I,C0398621,C580017,,,,Hypoplasminogenemia | Plasminogen deficiency | Hypoplasminogenaemia | Hypoplasminogenemia (disorder)
+BMGC_DS06341,BMG_DS019710,191302007;234467004,Thrombophilia,Thrombophilia,,,,DOID:2452,thrombophilia,C0398623,D019851,MTHU054815,MONDO:0002305,thrombophilia,Thrombophilia | Thrombophilia (disorder)
+BMGC_DS06342,BMG_DS019711,,Protein C Deficiency,Protein C Deficiency,,,,DOID:3756,protein C deficiency,C0398625,D020151,,,,
+BMGC_DS06343,BMG_DS019712,234468009,Heparin cofactor II deficiency (disorder),,,,,DOID:0111901,heparin cofactor II deficiency,C0398626,,612356,MONDO:0012876,heparin cofactor 2 deficiency,Heparin cofactor II deficiency | Heparin cofactor II deficiency (disorder)
+BMGC_DS06344,BMG_DS019719,234477002,Thromboxane synthetase deficiency,,,,,,,C0398635,,614158,MONDO:0013597,platelet-type bleeding disorder 14,Thromboxane synthetase deficiency | Thromboxane synthetase deficiency (disorder)
+BMGC_DS06345,BMG_DS019732,234490009;32273002,Immune thrombocytopenic purpura,,3B64.10,Immune thrombocytopenic purpura,D69.3,DOID:8924,autoimmune thrombocytopenic purpura,C0398650,,188030,MONDO:0008558,autoimmune thrombocytopenic purpura,Immune thrombocytopenic purpura | Immune thrombocytopenic purpura (disorder) | Idiopathic thrombocytopenic purpura | Immune thrombocytopenic purpura | ITP - immune thrombocytopenic purpura | Immune thrombocytopenic purpura (disorder)
+BMGC_DS06346,BMG_DS019737,191382009,Chronic congestive splenomegaly,,3B81.C,Chronic congestive splenomegaly,D73.2,DOID:11787,chronic congestive splenomegaly,C0398661,,,MONDO:0001367,chronic congestive splenomegaly,Chronic congestive splenomegaly (disorder) | Chronic congestive splenomegaly
+BMGC_DS06347,BMG_DS019749,111936002,Cerebral sarcoidosis,,,,,DOID:13403,neurosarcoidosis,C0398676,,,MONDO:0001706,cerebral sarcoidosis,Cerebral sarcoidosis | Cerebral sarcoidosis (disorder)
+BMGC_DS06348,BMG_DS019757,58606001,Primary immune deficiency disorder,,,,,,,C0398686,,,MONDO:0003778,inborn error of immunity,Primary immune deficiency disorder | Primary immune deficiency disorder (disorder) | Primary immunodeficiency
+BMGC_DS06349,BMG_DS019760,,"Hyper-IgM Immunodeficiency Syndrome, Type 1","Hyper-IgM Immunodeficiency Syndrome, Type 1",,,,DOID:6620,X-linked hyper IgM syndrome,C0398689,D053307,308230,MONDO:0010626,hyper-IgM syndrome type 1,
+BMGC_DS06350,BMG_DS019761,,Hyperimmunoglobulinemia D,Mevalonate Kinase Deficiency,,,,DOID:0050452,mevalonic aciduria,C0398691,D054078,260920,MONDO:0009849,hyperimmunoglobulinemia D with periodic fever,
+BMGC_DS06351,BMG_DS019763,234540007,Selective immunoglobulin E deficiency,,,,,DOID:6024,selective IgE deficiency disease,C0398694,,,MONDO:0003738,selective IgE deficiency disease,Selective IgE deficiency | Selective immunoglobulin E deficiency | Selective immunoglobulin E deficiency (disorder)
+BMGC_DS06352,BMG_DS019764,234541006,Selective immunoglobulin D deficiency,,,,,DOID:7263,selective IgD deficiency disease,C0398695,,,MONDO:0004165,selective IgD deficiency disease,Selective immunoglobulin D deficiency | Selective IgD deficiency | Selective immunoglobulin D deficiency (disorder)
+BMGC_DS06353,BMG_DS019778,,Secretory Component Deficiency,,,,,,,C0398709,C562869,269650,MONDO:0010019,secretory component deficiency,
+BMGC_DS06354,BMG_DS019799,,Leukocyte adhesion deficiency type 1,,,,,,,C0398738,C535887,116920,MONDO:0007293,leukocyte adhesion deficiency 1,
+BMGC_DS06355,BMG_DS019800,,"Congenital disorder of glycosylation, type 2C",,,,,DOID:0070255,congenital disorder of glycosylation type IIc,C0398739,C535755,266265,MONDO:0009953,leukocyte adhesion deficiency type II,
+BMGC_DS06356,BMG_DS019801,,Tuftsin Deficiency,,,,,,,C0398741,C562872,191150,MONDO:0008613,Tuftsin deficiency,
+BMGC_DS06357,BMG_DS019805,234589002,Gluthathione synthetase deficiency,,,,,,,C0398746,,266130,MONDO:0009947,glutathione synthetase deficiency with 5-oxoprolinuria,Glutathione synthetase deficiency | Glutathione synthetase deficiency (disorder) | Pyroglutamicaciduria
+BMGC_DS06358,BMG_DS019806,234590006,Gluthathione peroxidase deficiency,,,,,,,C0398747,,614164,MONDO:0013601,gluthathione peroxidase deficiency,Gluthathione peroxidase deficiency | Gluthathione peroxidase deficiency (disorder)
+BMGC_DS06359,BMG_DS019808,234593008,Classical complement pathway abnormality,,,,,,,C0398750,,,MONDO:0015699,immunodeficiency due to a classical component pathway complement deficiency,Classical complement pathway abnormality | Classical complement pathway abnormality (disorder)
+BMGC_DS06360,BMG_DS019820,81166004,Properdin deficiency disease,,,,,DOID:0111768,X-linked properdin deficiency,C0398762,,,,,Properdin deficiency disease | Properdin deficiency | Properdin deficiency disease (disorder)
+BMGC_DS06361,BMG_DS019822,,Complement Factor D Deficiency,,,,,,,C0398764,C565027,613912,MONDO:0013487,recurrent Neisseria infections due to factor D deficiency,
+BMGC_DS06362,BMG_DS019823,234608003,Terminal component deficiency,,,,,,,C0398765,,,MONDO:0015700,immunodeficiency due to a late component of complement deficiency,Terminal component deficiency | Terminal component deficiency (disorder)
+BMGC_DS06363,BMG_DS019833,234619000,Hereditary C1 esterase inhibitor deficiency - deficient factor,,,,,,,C0398775,,,,,Hereditary C1 esterase inhibitor deficiency - deficient factor | C1 esterase inhibitor deficiency - type 1 | Hereditary angioneurotic oedema - type 1 | Hereditary angio-oedema - type 1 | Hereditary angioneurotic edema - type 1 | Hereditary C1 esterase inhibitor deficiency - deficient factor (disorder) | Hereditary angioedema - type 1
+BMGC_DS06364,BMG_DS019834,234620006,Hereditary C1 esterase inhibitor deficiency - dysfunctional factor,,,,,,,C0398776,,,MONDO:0015054,hereditary angioedema type 2,Hereditary angioneurotic edema - type 2 | Hereditary angio-oedema - type 2 | Hereditary angioneurotic oedema - type 2 | C1 esterase inhibitor deficiency - type 2 | Hereditary C1 esterase inactivity | Hereditary C1 esterase inhibitor deficiency - dysfunctional factor | Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder) | Hereditary angioedema - type 2
+BMGC_DS06365,BMG_DS019835,,Complement Factor H Deficiency,,,,,,,C0398777,C562875,609814,MONDO:0012350,complement factor H deficiency,
+BMGC_DS06366,BMG_DS019840,,Carboxypeptidase N Deficiency,,,,,DOID:0111583,carboxypeptidase N deficiency,C0398782,C562876,212070,MONDO:0008910,carboxypeptidase N deficiency,
+BMGC_DS06367,BMG_DS019846,,"Immunodeficiency syndrome, variable",,,,,,,C0398788,C537362,,MONDO:0000133,immunodeficiency-centromeric instability-facial anomalies syndrome,
+BMGC_DS06368,BMG_DS019849,,Nijmegen Breakage Syndrome,Nijmegen Breakage Syndrome,,,,DOID:7400,Nijmegen breakage syndrome,C0398791,D049932,251260,MONDO:0009623,Nijmegen breakage syndrome,
+BMGC_DS06369,BMG_DS019852,37548006,Hypopigmentation-immunodeficiency disease,,,,,,,C0398794,,,MONDO:0018306,Griscelli syndrome,Hypopigmentation-immunodeficiency disease | Griscelli syndrome | Chediak-Higashi-like syndrome | Griscelli syndrome with immunodeficiency | Partial albinism with immunodeficiency | Hypopigmentation-immunodeficiency disease (disorder)
+BMGC_DS06370,BMG_DS019858,,Other diseases of hard tissues of teeth,,,,K03,,,C0399347,,,,,
+BMGC_DS06371,BMG_DS019859,,,,,,,DOID:0050591;DOID:13714,anodontia | tooth agenesis,C0399352,,206780,MONDO:0008797,anodontia,
+BMGC_DS06372,BMG_DS019864,,,,,,,,,C0399367,,,MONDO:0015047,amelogenesis imperfecta type 1,
+BMGC_DS06373,BMG_DS019865,,"Amelogenesis Imperfecta, Type IB",,,,,,,C0399368,C562879,104500,MONDO:0007092,amelogenesis imperfecta type 1B,
+BMGC_DS06374,BMG_DS019866,,,,,,,,,C0399372,,,MONDO:0015048,amelogenesis imperfecta type 2,
+BMGC_DS06375,BMG_DS019867,109472008,"Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism",,,,,,,C0399373,,,,,"Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism | Amelogenesis imperfecta - hypomaturation - autosomal dominant - hypoplastic with taurodontism | Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism (disorder)"
+BMGC_DS06376,BMG_DS019868,,"Amelogenesis Imperfecta, Type III",,,,,DOID:0111721,amelogenesis imperfecta type 3,C0399376,C562880,,MONDO:0968955,hypocalcified amelogenesis imperfecta,
+BMGC_DS06377,BMG_DS019870,,,,,,,,,C0399378,,125500,MONDO:0007442,dentinogenesis imperfecta type 3,
+BMGC_DS06378,BMG_DS019871,,"Dentin dysplasia, type 1",,,,,,,C0399379,C538215,125400,MONDO:0007436,dentin dysplasia type I,
+BMGC_DS06379,BMG_DS019879,234977009,Tooth surface loss,,,,,DOID:2497,enamel erosion,C0399400,,,,,Tooth surface loss | Tooth substance loss | Tooth surface loss (disorder)
+BMGC_DS06380,BMG_DS019898,109620006,Hereditary gingival fibromatosis,,,,,DOID:0060466,gingival fibromatosis,C0399440,,,MONDO:0016070,hereditary gingival fibromatosis,Hereditary gingival fibromatosis | Hereditary fibrous enlargement of gingiva | Hereditary gingival fibromatosis (disorder)
+BMGC_DS06381,BMG_DS019931,,,,,,,,,C0399526,,176700,MONDO:0008312,autosomal dominant prognathism,
+BMGC_DS06382,BMG_DS019957,,,,,,,,,C0399605,,120500,MONDO:0007359,commissural lip pits,
+BMGC_DS06383,BMG_DS019965,,"Colitis, Microscopic","Colitis, Microscopic",,,,DOID:0060182,microscopic colitis,C0400821,D046728,,MONDO:0000702,microscopic colitis,
+BMGC_DS06384,BMG_DS019966,,"Colitis, Lymphocytic","Colitis, Lymphocytic",,,,DOID:0060184,lymphocytic colitis,C0400822,D046730,,MONDO:0000704,lymphocytic colitis,
+BMGC_DS06385,BMG_DS019967,235755005,Neutropenic colitis,,,,,,,C0400823,,,,,Neutropenic colitis | Neutropenic colitis (disorder)
+BMGC_DS06386,BMG_DS019972,,Ulcer of anus and rectum,,DB52,Ulcer of anus,K62.6,DOID:13662,ulcer of anus and rectum,C0400832,,,MONDO:0001772,ulcer of anus and rectum,
+BMGC_DS06387,BMG_DS019991,235833007,Postoperative ileus,,,,,,,C0400877,,,,,Postoperative ileus | Postoperative ileus (disorder)
+BMGC_DS06388,BMG_DS020017,235866006,Acute hepatitis C,,1E50.2,Acute hepatitis C,B17.1,,,C0400914,,,,,Acute hepatitis C | Acute hepatitis C (disorder)
+BMGC_DS06389,BMG_DS020020,186638006;235869004,Chronic viral hepatitis B with hepatitis D,,,,,,,C0400918,,,,,Chronic viral hepatitis B with hepatitis D | Chronic viral hepatitis B with hepatitis D (disorder) | Chronic viral hepatitis B with hepatitis D | Chronic viral hepatitis B with delta-agent | Chronic viral hepatitis B with hepatitis D (disorder)
+BMGC_DS06390,BMG_DS020022,235878005,Vascular disorder of liver,,,,,DOID:272,hepatic vascular disease,C0400923,,,MONDO:0002405,hepatic vascular disorder,Vascular disorder of liver | Vascular disorder of liver (disorder)
+BMGC_DS06391,BMG_DS020054,,"Hyperbilirubinemia, Conjugated, Type III",,,,,,,C0400964,C562885,237550,MONDO:0009381,"hyperbilirubinemia, conjugated, type 3",
+BMGC_DS06392,BMG_DS020056,,Non-alcoholic Fatty Liver Disease,Non-alcoholic Fatty Liver Disease,,,,DOID:0080208,metabolic dysfunction-associated steatotic liver disease,C0400966,D065626,,MONDO:0013209,metabolic dysfunction-associated steatotic liver disease,
+BMGC_DS06393,BMG_DS020112,197034002;236071009,Chronic diarrhea,,,,,,,C0401151,,MTHU004140,MONDO:0044751,chronic diarrheal disease,(Chronic diarrhoea) or (other non-infective gastroenteritis and colitis NOS) | Chronic diarrhoea | Chronic diarrhea | (Chronic diarrhea) or (other non-infective gastroenteritis and colitis NOS) | Other non-infective gastroenteritis and colitis NOS | (Chronic diarrhoea) or (other non-infective gastroenteritis and colitis NOS) (disorder) | Chronic diarrhea | Chronic diarrhoea | Chronic diarrhea (disorder)
+BMGC_DS06394,BMG_DS020150,,Steroid-Sensitive Nephrotic Syndrome,Nephrotic Syndrome,,,,,,C0403396,D009404,,MONDO:0044781,nephrotic syndrome of childhood - steroid sensitive,
+BMGC_DS06395,BMG_DS020151,236381000,Steroid-resistant nephrotic syndrome,,,,,,,C0403397,,MTHU062745,MONDO:0044765,steroid-resistant nephrotic syndrome,Steroid-unresponsive nephrotic syndrome | SRNS - Steroid-resistant nephrotic syndrome | Steroid-resistant nephrotic syndrome | Steroid-resistant nephrotic syndrome (disorder)
+BMGC_DS06396,BMG_DS020152,,Steroid-Dependent Nephrotic Syndrome,Nephrotic Syndrome,,,,,,C0403398,D009404,,,,
+BMGC_DS06397,BMG_DS020153,197601003,Finnish congenital nephrotic syndrome,,,,,DOID:0080390,nephrotic syndrome type 1,C0403399,,256300,MONDO:0009732,"congenital nephrotic syndrome, Finnish type",Finnish congenital nephrotic syndrome | CNF - Finnish congenital nephrotic syndrome | Congenital Finnish nephrosis | Finnish congenital nephrotic syndrome (disorder)
+BMGC_DS06398,BMG_DS020165,68544003,Acute post-streptococcal glomerulonephritis,,,,,DOID:14064,acute poststreptococcal glomerulonephritis,C0403414,,,MONDO:0001870,acute poststreptococcal glomerulonephritis,Acute post-streptococcal glomerulonephritis | Post-streptococcal glomerulonephritis | PSGN - post-streptococcal glomerulonephritis | Acute glomerulonephritis due to and following streptococcal infection | Acute glomerulonephritis due to and following streptococcal infection (disorder)
+BMGC_DS06399,BMG_DS020167,45406000;236398000,Idiopathic crescentic glomerulonephritis,,,,,DOID:13139,crescentic glomerulonephritis,C0403416,,,MONDO:0001645,crescentic glomerulonephritis,Idiopathic crescentic glomerulonephritis | Idiopathic crescentic glomerulonephritis (disorder) | Idiopathic crescentic glomerulonephritis | Crescentic glomerulonephritis | CGN - Crescentic glomerulonephritis | Crescentic glomerulonephritis (disorder) | Proliferative crescentic glomerulonephritis
+BMGC_DS06400,BMG_DS020189,,"Renal Failure, Progressive, with Hypertension",,,,,,,C0403443,C562889,161900,MONDO:0008071,autosomal dominant progressive nephropathy with hypertension,
+BMGC_DS06401,BMG_DS020192,,Chronic Kidney Insufficiency,"Renal Insufficiency, Chronic",,,,,,C0403447,D051436,,,,
+BMGC_DS06402,BMG_DS020202,236435004,End stage renal failure on dialysis,,,,,,,C0403464,,,,,End stage renal failure on dialysis | End stage renal failure on dialysis (disorder)
+BMGC_DS06403,BMG_DS020205,,,,,,,,,C0403468,,,MONDO:0041295,acute papillary necrosis,
+BMGC_DS06404,BMG_DS020247,236503001,Acute scleroderma renal crisis,,,,,,,C0403527,,,,,Acute scleroderma renal crisis | Acute scleroderma renal crisis (disorder)
+BMGC_DS06405,BMG_DS020249,,Anti-Glomerular Basement Membrane Disease,Anti-Glomerular Basement Membrane Disease,,,,DOID:9808,Goodpasture syndrome,C0403529,D019867,233450,MONDO:0009303,anti-glomerular basement membrane disease,
+BMGC_DS06406,BMG_DS020267,,Salcedo syndrome,,,,,,,C0403548,C537228,256020,MONDO:0009724,nail-patella-like renal disease,
+BMGC_DS06407,BMG_DS020269,,"Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness",,,,,,,C0403551,C562894,264140,MONDO:0009913,"prune belly syndrome with pulmonic stenosis, intellectual disability, and deafness",
+BMGC_DS06408,BMG_DS020271,236531005,Renal dysplasia and retinal aplasia (disorder),,,,,,,C0403553,,,MONDO:0017842,Senior-Loken syndrome,Renal dysplasia and retinal aplasia | Loken Senior syndrome | Renal dysplasia and retinal aplasia (disorder)
+BMGC_DS06409,BMG_DS020272,,"Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness",,,,,,,C0403554,C562897,267300,MONDO:0009968,"renal tubular acidosis, distal, 2, with progressive sensorineural hearing loss",
+BMGC_DS06410,BMG_DS020273,236533008,Ochoa syndrome,,,,,DOID:0050816,urofacial syndrome,C0403555,C536480,,MONDO:0000463,Ochoa syndrome,Ochoa syndrome | Ochoa syndrome (disorder)
+BMGC_DS06411,BMG_DS020275,,Glomerulopathy with Giant Fibrillar Deposits,,,,,,,C0403557,C562900,137950,MONDO:0024527,glomerulopathy with fibronectin deposits 1,
+BMGC_DS06412,BMG_DS020277,87235005,Dialysis disequilibrium syndrome,,,,,DOID:0070564,dialysis disequilibrium syndrome,C0403559,,,,,Dialysis disequilibrium syndrome | Dialysis disequilibrium | Dialysis disequilibrium syndrome (disorder) | Dialysis dysequilibrium syndrome | DDS - dialysis disequilibrium syndrome
+BMGC_DS06413,BMG_DS020282,236552002,Adynamic bone disease,,,,,,,C0403566,,,,,Adynamic bone disease | Adynamic bone disease (disorder) | Aplastic bone disease
+BMGC_DS06414,BMG_DS020307,128073008,Disorder of ureter,,,,,DOID:1426,ureteral disease,C0403608,,,MONDO:0001926,ureteral disorder,Disorder of ureter | Disorder of ureter (disorder)
+BMGC_DS06415,BMG_DS020323,,,,,,,,,C0403653,,,MONDO:0041154,disorder of neck of urinary bladder,
+BMGC_DS06416,BMG_DS020324,236645006,Obstruction of urinary bladder outflow,,,,,,,C0403654,,,,,Bladder outflow obstruction | Obstruction of urinary bladder outflow (disorder) | Obstruction of urinary bladder outflow | BOO - bladder outflow obstruction
+BMGC_DS06417,BMG_DS020346,267441009,Uric acid urolithiasis,,,,,DOID:580,uric acid nephrolithiasis,C0403719,,MTHU037371,,,Uric acid urolithiasis | Uric acid urolithiasis (disorder)
+BMGC_DS06418,BMG_DS020347,236713006,X-linked recessive nephrolithiasis with renal failure,,,,,,,C0403720,,310468,MONDO:0010687,"nephrolithiasis, X-linked recessive, with renal failure",X-linked recessive nephrolithiasis with renal failure | X-linked recessive nephrolithiasis with renal failure (disorder)
+BMGC_DS06419,BMG_DS020353,236738001,Perforation of uterus caused by intrauterine contraceptive device,,,,,,,C0403745,,,,,Uterine perforation by intrauterine contraceptive device | Perforation of uterus caused by intrauterine contraceptive device (disorder) | Perforation of uterus caused by intrauterine contraceptive device | IUD (intrauterine contraceptive device) perforation of uterus | IUCD (intrauterine contraceptive device) perforation of uterus
+BMGC_DS06420,BMG_DS020385,,Oligosynaptic Infertility,,,,,,,C0403810,C562902,258150,MONDO:0009776,spermatogenic failure 1,
+BMGC_DS06421,BMG_DS020386,236805000,Congenital impairment of spermatozoa motility,,,,,,,C0403811,,,,,Congenital impairment of sperm motility | Congenital impairment of spermatozoa motility (disorder) | Congenital impairment of spermatozoa motility
+BMGC_DS06422,BMG_DS020387,,"Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa",,,,,DOID:0070183,spermatogenic failure 5,C0403812,C562903,243060,MONDO:0009461,spermatogenic failure 5,
+BMGC_DS06423,BMG_DS020388,,,,,,,,,C0403814,,277180,MONDO:0010178,congenital bilateral aplasia of vas deferens from CFTR mutation,
+BMGC_DS06424,BMG_DS020395,,Asthenozoospermia,Asthenozoospermia,,,,,,C0403823,D053627,MTHU062248,,,
+BMGC_DS06425,BMG_DS020396,236817003,Teratozoospermia,Teratozoospermia,,,,DOID:0070167,spermatogenic failure 6,C0403824,D000072660,MTHU064721,,,Teratozoospermia | Teratozoospermia (disorder)
+BMGC_DS06426,BMG_DS020397,,,,,,,,,C0403825,,102530,MONDO:0007060,spermatogenic failure 6,
+BMGC_DS06427,BMG_DS020698,198113009,Pubertal breast hypertrophy,,,,,,,C0405471,,113670,MONDO:0007237,familial juvenile hypertrophy of the breast,Pubertal breast hypertrophy | Diffuse hypertrophy of breast | Juvenile mammary hypertrophy | Pubertal breast hypertrophy (disorder) | Adolescent macromastia
+BMGC_DS06428,BMG_DS020710,68588005;386584007,Adrenal cortical hypofunction,,,,,DOID:10493,adrenal cortical hypofunction,C0405580,,,MONDO:0000004,adrenocortical insufficiency,Adrenal cortical hypofunction | Hypoadrenocorticism | Corticoadrenal insufficiency | Adrenal insufficiency | Adrenocortical hypofunction | Primary hypoadrenalism | Adrenal cortical hypofunction (disorder) | Adrenal cortical hypofunction (disorder) | Adrenal cortical hypofunction | Adrenocortical hypofunction | Hypoadrenocorticism | Adrenal insufficiency | Corticoadrenal insufficiency
+BMGC_DS06429,BMG_DS020803,402128003;238420008,Cutaneous listeriosis,,1C1A.0,Cutaneous listeriosis,A32.0,,,C0406143,,,,,Cutaneous listeriosis (disorder) | Cutaneous listeriosis | Cutaneous involvement by listeriosis | Cutaneous listeriosis | Cutaneous involvement in listeriosis | Cutaneous involvement in listeriosis (disorder)
+BMGC_DS06430,BMG_DS020819,27687007;201015007,Actinic prurigo,,,,,,,C0406217,,174770,MONDO:0008273,actinic prurigo,Hydroa aestivale | Hydroa vacciniforme | Summer prurigo of Hutchinson | Hydroa estivale | Actinic prurigo | Hutchinson's summer prurigo | Bazin's hydroa vacciniforme | Hydroa estivale (disorder) | Actinic prurigo | Actinic prurigo (disorder) | Summer prurigo of Hutchinson | Hutchinson's summer prurigo | Familial actinic prurigo | Hydroa estivale | Hydroa aestivale | Hereditary polymorphous light eruption of American Indians | Familial polymorphous light eruption of American Indians
+BMGC_DS06431,BMG_DS020869,402308005,Chronic small plaque psoriasis,,,,,,,C0406317,,,,,Chronic small plaque psoriasis (disorder) | Chronic small plaque psoriasis
+BMGC_DS06432,BMG_DS020878,238608008,Psoriasis of scalp,,,,,,,C0406326,,,,,Scalp psoriasis | Psoriasis of scalp (disorder) | Psoriasis of scalp
+BMGC_DS06433,BMG_DS020924,238662007,Erosive oral lichen planus,,,,,,,C0406378,,,,,Erosive oral lichen planus | Erosive oral lichen planus (disorder)
+BMGC_DS06434,BMG_DS020967,,,,,,,,,C0406443,,161050,MONDO:0008060,nonsyndromic congenital nail disorder 1,
+BMGC_DS06435,BMG_DS020985,,Loose Anagen Hair Syndrome,Loose Anagen Hair Syndrome,,,,DOID:0111702,loose anagen hair syndrome,C0406468,D058247,600628,MONDO:0010908,loose anagen syndrome,
+BMGC_DS06436,BMG_DS021001,,Ocular Rosacea,Rosacea,,,,,,C0406486,D012393,,,,
+BMGC_DS06437,BMG_DS021013,238764001,Hereditary benign telangiectasia (disorder),,,,,,,C0406502,,187260,MONDO:0008534,generalized essential telangiectasia,Hereditary benign telangiectasia | Hereditary benign telangiectasia (disorder)
+BMGC_DS06438,BMG_DS021034,201251005,Neuropathic ulcer of foot due to diabetes mellitus,,,,,,,C0406526,,,,,Neuropathic diabetic ulcer - foot | Neuropathic ulcer of foot due to diabetes mellitus (disorder) | Neuropathic ulcer of foot due to diabetes mellitus
+BMGC_DS06439,BMG_DS021044,,Morbilliform Drug Reaction,Drug Eruptions,,,,,,C0406537,D003875,,,,
+BMGC_DS06440,BMG_DS021059,238836000,Poikiloderma of Kindler,,,,,DOID:0060472,Kindler syndrome,C0406557,C536321,173650,MONDO:0008260,Kindler syndrome,Kindler's syndrome | Kindler syndrome | Kindler epidermolysis bullosa (disorder) | Kindler epidermolysis bullosa | Poikiloderma of Kindler | Congenital bullous poikiloderma
+BMGC_DS06441,BMG_DS021061,,Pseudoatrophoderma Colli,,,,,,,C0406561,C562909,177350,MONDO:0008325,Pseudoatrophoderma colli,
+BMGC_DS06442,BMG_DS021074,400128006,Lethal tight skin contracture syndrome (disorder),,,,,DOID:0060762,restrictive dermopathy,C0406585,,,MONDO:0031213,restrictive dermopathy,Lethal tight skin contracture syndrome (disorder) | Lethal tight skin contracture syndrome | Infantile restrictive dermopathy
+BMGC_DS06443,BMG_DS021075,238874008,Wiedemann-Rautenstrauch syndrome,,,,,,,C0406586,C536423,264090,MONDO:0009910,Wiedemann-Rautenstrauch syndrome,Neonatal pseudo-hydrocephalic progeroid syndrome | Wiedemann-Rautenstrauch syndrome | Neonatal pseudo-hydrocephalic progeroid syndrome (disorder)
+BMGC_DS06444,BMG_DS021076,238875009,Wrinkly skin syndrome,,,,,DOID:0112171,wrinkly skin syndrome,C0406587,C536750,278250,MONDO:0010208,wrinkly skin syndrome,WSS - Wrinkly skin syndrome | Wrinkly skin syndrome | Wrinkly skin syndrome (disorder)
+BMGC_DS06445,BMG_DS021091,,,,,,,DOID:3927,pelvic lipomatosis,C0406608,,,MONDO:0006593,pelvic lipomatosis,
+BMGC_DS06446,BMG_DS021093,,,,,,,,,C0406612,,613001,MONDO:0013074,encephalocraniocutaneous lipomatosis,
+BMGC_DS06447,BMG_DS021114,403491004,Erythema multiforme-like lupus erythematosus,,,,,,,C0406637,,,MONDO:0041186,Rowell syndrome,Erythema multiforme-like lupus erythematosus (disorder) | Erythema multiforme-like lupus erythematosus | Rowell syndrome
+BMGC_DS06448,BMG_DS021145,238985006,Bullous pyoderma gangrenosum,,,,,,,C0406687,,,MONDO:0035237,bullous pyoderma gangrenosum,Bullous pyoderma | Bullous pyoderma gangrenosum | Bullous pyoderma gangrenosum (disorder)
+BMGC_DS06449,BMG_DS021156,,,,,,,,,C0406702,,,MONDO:0016619,autosomal recessive hypohidrotic ectodermal dysplasia,
+BMGC_DS06450,BMG_DS021157,,Rudiger syndrome 1,,,,,DOID:0060784;DOID:0060782;DOID:0060783,"ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 | ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 | EEC syndrome",C0406704,C536189,268650,MONDO:0010004,EEC syndrome,
+BMGC_DS06451,BMG_DS021158,239011004,Basan syndrome,,,,,DOID:0080725,BASAN syndrome,C0406707,C537659,129200,MONDO:0007507,absence of fingerprints-congenital milia syndrome,Basan syndrome | Basan syndrome (disorder)
+BMGC_DS06452,BMG_DS021159,55821006,Hay-Wells syndrome,,,,,,,C0406709,C535847,106260,MONDO:0007124,ankyloblepharon-ectodermal defects-cleft lip/palate syndrome,"Hay-Wells syndrome of ectodermal dysplasia | Ankyloblepharon-ectodermal dysplasia-clefting syndrome | AEC syndrome | Hay-Wells syndrome of ectodermal dysplasia (disorder) | Hay-Wells syndrome | AEC - Ankyloblepharon, ectodermal defects, cleft lip and palate | Ankyloblepharon, ectodermal defects, cleft lip and palate | Hay Wells syndrome of ectodermal dysplasia"
+BMGC_DS06453,BMG_DS021161,239020008,Fried's tooth and nail syndrome,,,,,DOID:0111661,ectodermal dysplasia 8,C0406715,,,,,Fried's tooth and nail syndrome | Fried's tooth and nail syndrome (disorder) | Fried tooth and nail syndrome
+BMGC_DS06454,BMG_DS021162,,,,,,,,,C0406718,,278200,MONDO:0010207,wooly hair-hypotrichosis-everted lower lip-outstanding ears syndrome,
+BMGC_DS06455,BMG_DS021164,,"Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy",,,,,,,C0406723,C535642,230740,MONDO:0009263,GAPO syndrome,
+BMGC_DS06456,BMG_DS021165,277810000,Trichodental syndrome,,,,,,,C0406724,C536551,601453,MONDO:0011083,trichodental syndrome,Trichodental syndrome | Trichodental syndrome (disorder)
+BMGC_DS06457,BMG_DS021166,,Orofaciodigital syndrome 3,,,,,DOID:0060373,orofaciodigital syndrome III,C0406726,C557817,258850,MONDO:0009793,orofaciodigital syndrome III,
+BMGC_DS06458,BMG_DS021167,,Orofaciodigital syndrome 4,,,,,DOID:0060374,orofaciodigital syndrome IV,C0406727,C537133,258860,MONDO:0009794,orofaciodigital syndrome IV,
+BMGC_DS06459,BMG_DS021170,,Curly hair-ankyloblepharon-nail dysplasia syndrome,,,,,,,C0406733,C538074,214350,MONDO:0008959,CHAND syndrome,
+BMGC_DS06460,BMG_DS021172,400036004,Hypoplastic enamel-onycholysis-hypohidrosis syndrome,,,,,DOID:6678,tooth and nail syndrome,C0406735,,189500,MONDO:0008582,tooth and nail syndrome,Hypoplastic enamel-onycholysis-hypohidrosis syndrome (disorder) | Hypoplastic enamel-onycholysis-hypohidrosis syndrome | Witkop-Brearley-Gentry syndrome
+BMGC_DS06461,BMG_DS021176,,Kohlschutter Tonz syndrome,,,,,DOID:0111668,Kohlschutter-Tonz syndrome,C0406740,C537213,226750,MONDO:0009185,amelocerebrohypohidrotic syndrome,
+BMGC_DS06462,BMG_DS021183,239064000,Keratolytic winter erythema,,,,,,,C0406756,C536155,148370,MONDO:0007854,keratolytic winter erythema,Oudtshoorn disease | Winter erythrokeratolysis | Erythrokeratolysis hiemalis | Keratolytic winter erythema | Keratolytic winter erythema (disorder)
+BMGC_DS06463,BMG_DS021184,,,,,,,,,C0406757,,,MONDO:0019272,hereditary palmoplantar keratoderma,
+BMGC_DS06464,BMG_DS021185,239072003,Congenital palmoplantar and perioral keratoderma of Olmsted,,,,,,,C0406761,,,MONDO:0031421,Olmsted syndrome,Congenital palmoplantar and perioral keratoderma of Olmsted | Congenital palmoplantar and perioral keratoderma of Olmsted (disorder) | Olmsted syndrome | Mutilating palmoplantar hyperkeratosis with periorificial keratotic plaques
+BMGC_DS06465,BMG_DS021189,,,,,,,,,C0406767,,181600,MONDO:0008416,palmoplantar keratoderma-sclerodactyly syndrome,
+BMGC_DS06466,BMG_DS021193,,,,,,,DOID:0060257,dyschromatosis symmetrica hereditaria,C0406775,,127400,MONDO:0007483,dyschromatosis symmetrica hereditaria,
+BMGC_DS06467,BMG_DS021195,,,,,,,DOID:0111342,dermatopathia pigmentosa reticularis,C0406778,,125595,MONDO:0007445,dermatopathia pigmentosa reticularis,
+BMGC_DS06468,BMG_DS021210,,,,,,,DOID:5445,syringocystadenoma papilliferum,C0406803,,,MONDO:0019392,syringocystadenoma papilliferum,
+BMGC_DS06469,BMG_DS021213,,Carney Complex,Carney Complex,,,,DOID:0050471,Carney complex,C0406810,D056733,,MONDO:0015285,Carney complex,
+BMGC_DS06470,BMG_DS021214,239133004,Reticulate acropigmentation of Kitamura,,,,,DOID:0060258;DOID:0060256,reticulate acropigmentation of Kitamura | Dowling-Degos disease,C0406811,,615537,MONDO:0014234,reticulate acropigmentation of Kitamura,Kitamura's reticulate acropigmentation | Reticulate acropigmentation of Kitamura | Reticulate acropigmentation of Kitamura (disorder)
+BMGC_DS06471,BMG_DS021215,,,,,,,,,C0406817,,115250,MONDO:0007271,familial cutaneous collagenoma,
+BMGC_DS06472,BMG_DS021216,,,,,,,,,C0406819,,,MONDO:0016986,congenital smooth muscle hamartoma,
+BMGC_DS06473,BMG_DS021275,,,,,,,,,C0409495,,177050,MONDO:0008320,Protrusio acetabuli,
+BMGC_DS06474,BMG_DS021401,,,,,,,DOID:676,juvenile rheumatoid arthritis,C0409667,,,MONDO:0024281,juvenile chronic polyarthritis,
+BMGC_DS06475,BMG_DS021407,201802002;239805001,Juvenile ankylosing spondylitis,,FA9Z,"Inflammation of spine, unspecified",M08.1,DOID:0040092,juvenile ankylosing spondylitis,C0409675,,,MONDO:0020655,juvenile ankylosing spondylitis,Juvenile ankylosing spondylitis | Juvenile ankylosing spondylitis (disorder) | Juvenile ankylosing spondylitis | AS - Juvenile ankylosing spondylitis | Juvenile ankylosing spondylitis (disorder)
+BMGC_DS06476,BMG_DS021499,,"Chronic Infantile Neurological, Cutaneous, and Articular Syndrome",Cryopyrin-Associated Periodic Syndromes,,,,,,C0409818,D056587,607115,MONDO:0011776,CINCA syndrome,
+BMGC_DS06477,BMG_DS021602,,"Osteoarthritis, Knee","Osteoarthritis, Knee",,,,,,C0409959,D020370,,MONDO:0005416,"osteoarthritis, knee",
+BMGC_DS06478,BMG_DS021614,,,,,,,DOID:8857,lupus erythematosus,C0409974,,,MONDO:0004670,lupus erythematosus,
+BMGC_DS06479,BMG_DS021639,703616008;268106003;156729009;400138001;35548007,Nodular fasciitis,,FB51.2,Fasciitis and fibromatosis,M72.4,DOID:7327,pseudosarcomatous fibromatosis,C0410005,,,MONDO:0004187,nodular fasciitis,"Nodular fasciitis (morphologic abnormality) | Nodular fasciitis | (Muscle/ligament disord NOS) or (lig contraction) or (musc contracture) or (nodular fasciitis) or (granuloma: [FB][talc]) or (hypotonia unsp) or (non-traum musc: [tear][rupt]) or (rhabdomyolysis) | Non-traumatic muscle tear | Non-traumatic muscle rupture | Muscle contracture | Nontraumatic muscle rupture | Foreign body granuloma | Rhabdomyolysis | Hypotonia, unspecified | Nodular fasciitis | Fasciitis - nodular | Contraction - ligament | Muscle/ligament disorder NOS | Talc granuloma | Granuloma -foreign body | (Muscle/ligament disord NOS) or (lig contraction) or (musc contracture) or (nodular fasciitis) or (granuloma: [FB][talc]) or (hypotonia unsp) or (non-traum musc: [tear][rupt]) or (rhabdomyolysis) (disorder) | (Muscle/ligament disord NOS) or (lig contraction) or (musc contracture) or (nodular fasciitis) or (granuloma: [FB][talc]) or (hypotonia unsp) or (non-traum musc: [tear][rupt]) or (rhabdomyolysis) | Muscle contracture | Rhabdomyolysis | Non-traumatic muscle tear | Granuloma -foreign body | Fasciitis - nodular | Non-traumatic muscle rupture | Contraction - ligament | Muscle/ligament disorder NOS | Nontraumatic muscle rupture | Foreign body granuloma | Nodular fasciitis | Hypotonia, unspecified | Talc granuloma | (Muscle/ligament disord NOS) or (lig contraction) or (musc contracture) or (nodular fasciitis) or (granuloma: [FB][talc]) or (hypotonia unsp) or (non-traum musc: [tear][rupt]) or (rhabdomyolysis) (disorder) | Nodular fasciitis (disorder) | Nodular fasciitis | Infiltrative fasciitis | Nodular fasciitis | Pseudosarcomatous fibromatosis | Pseudosarcomatous fasciitis | Proliferative fasciitis | Infiltrative fasciitis | Nodular fasciitis (disorder)"
+BMGC_DS06480,BMG_DS021661,,,,,,,,,C0410060,,190410,MONDO:0008600,trigger thumb,
+BMGC_DS06481,BMG_DS021665,203051006,"Dupuytren's disease of finger, with contracture",,,,,,,C0410065,,,,,"Dupuytren's disease of finger(s), with contracture | Dupuytren's disease of finger, with contracture | Dupuytren's disease of finger, with contracture (disorder) | Dupuytren disease of finger, with contracture"
+BMGC_DS06482,BMG_DS021732,240056002,Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder),,,,,,,C0410173,,253700,MONDO:0009677,autosomal recessive limb-girdle muscular dystrophy type 2C,Severe autosomal recessive muscular dystrophy of childhood - North African type | Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)
+BMGC_DS06483,BMG_DS021733,,Fukuyama Type Congenital Muscular Dystrophy,Walker-Warburg Syndrome,,,,DOID:0050560,Walker-Warburg syndrome,C0410174,D058494,253800,MONDO:0009678,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4",
+BMGC_DS06484,BMG_DS021738,,Ullrich congenital muscular dystrophy 1,,,,,,,C0410179,C537521,254090,MONDO:0009681,Ullrich congenital muscular dystrophy 1A,
+BMGC_DS06485,BMG_DS021739,240063002,Eichsfeld type congenital muscular dystrophy,,,,,,,C0410180,,602771,MONDO:0011271,rigid spine muscular dystrophy 1,Eichsfeld type congenital muscular dystrophy | Eichsfeld type congenital muscular dystrophy (disorder) | Rigid spine syndrome
+BMGC_DS06486,BMG_DS021746,,"Muscular Dystrophy, Emery-Dreifuss","Muscular Dystrophy, Emery-Dreifuss",,,,DOID:11726,Emery-Dreifuss muscular dystrophy,C0410189,D020389,,MONDO:0016830,Emery-Dreifuss muscular dystrophy,
+BMGC_DS06487,BMG_DS021747,,,,,,,,,C0410190,,159001;181350,MONDO:0021569,"Emery-Dreifuss muscular dystrophy 2, autosomal dominant",
+BMGC_DS06488,BMG_DS021749,,"Muscular Dystrophy, Scapulohumeral",,,,,,,C0410192,C562932,600416,MONDO:0010884,"muscular dystrophy, scapulohumeral",
+BMGC_DS06489,BMG_DS021759,,,,,,,DOID:0111225,centronuclear myopathy X-linked,C0410203,,310400,MONDO:0010683,X-linked myotubular myopathy,
+BMGC_DS06490,BMG_DS021760,,"Myopathy, Centronuclear, Autosomal Recessive",,,,,DOID:0111220,centronuclear myopathy 2,C0410204,C562934,255200,MONDO:0009709,"myopathy, centronuclear, 2",
+BMGC_DS06491,BMG_DS021763,,Tubular Aggregate Myopathy,"Myopathies, Structural, Congenital",,,,,,C0410207,D020914,,MONDO:0008051,tubular aggregate myopathy,
+BMGC_DS06492,BMG_DS021768,,Myopathy with Abnormal Lipid Metabolism,,,,,,,C0410214,C562935,,,,
+BMGC_DS06493,BMG_DS021777,,Congenital Myotonic Dystrophy,Myotonic Dystrophy,,,,,,C0410226,D009223,,MONDO:0023595,congenital myotonic dystrophy,
+BMGC_DS06494,BMG_DS021879,240151005;203203009,Chronic multifocal osteomyelitis,,FB84.Z,"Osteomyelitis or osteitis, unspecified",M86.3,DOID:0060645,chronic recurrent multifocal osteomyelitis,C0410422,C535456,,MONDO:0009813,chronic recurrent multifocal osteomyelitis,Chronic multifocal osteomyelitis | CRMO - Chronic multifocal osteomyelitis | Chronic multifocal osteomyelitis (disorder) | Chronic multifocal osteomyelitis | Chronic multifocal osteomyelitis (disorder)
+BMGC_DS06495,BMG_DS021943,105986008,Skeletal dysplasia,,,,,,,C0410528,,MTHU042509,MONDO:0018230,skeletal dysplasia,Skeletal dysplasia | Congenital skeletal dysplasia (disorder) | Congenital skeletal dysplasia | Osteochondrodysplasia | Osteodysplasia
+BMGC_DS06496,BMG_DS021944,205468002,Hypochondroplasia (disorder),,,,,DOID:0080041,hypochondroplasia,C0410529,,146000,MONDO:0007793,hypochondroplasia,Hypochondroplasia | Hypochondrodysplasia | Hypochondroplasia (disorder)
+BMGC_DS06497,BMG_DS021945,205481009,Metachondromatosis,,,,,DOID:0111512,metachondromatosis,C0410530,C562938,156250,MONDO:0007979,metachondromatosis,Metachondromatosis | Metachondromatosis (disorder)
+BMGC_DS06498,BMG_DS021949,,,,,,,,,C0410538,,177170,MONDO:0008322,pseudoachondroplasia,
+BMGC_DS06499,BMG_DS021950,205506004,Craniodiaphyseal dysplasia,,,,,,,C0410539,,218300,MONDO:0009031,craniodiaphyseal dysplasia,Craniodiaphyseal dysplasia | CDD - Craniodiaphyseal dysplasia | Craniodiaphyseal dysplasia (disorder)
+BMGC_DS06500,BMG_DS021974,,Synovial Hypertrophy,Synovitis,,,,,,C0410574,D013585,,,,
+BMGC_DS06501,BMG_DS021994,,,,,,,DOID:90,degenerative disc disease,C0410606,,,MONDO:0044343,cervical disk degenerative disorder,
+BMGC_DS06502,BMG_DS022238,,"Seizures, Somatosensory",Seizures,,,,,,C0422850,D012640,,,,
+BMGC_DS06503,BMG_DS022244,,Lazy Eye,Amblyopia,,,,,,C0422955,D000550,,,,
+BMGC_DS06504,BMG_DS022254,,Superior Oblique Myokymia,Trochlear Nerve Diseases,,,,DOID:13864,trochlear nerve disease,C0423092,D020432,,,,
+BMGC_DS06505,BMG_DS022255,,,,,,,,,C0423113,,187350,MONDO:0008537,telecanthus,
+BMGC_DS06506,BMG_DS022261,,,,,,,,,C0423224,,,MONDO:0001210,enophthalmos,
+BMGC_DS06507,BMG_DS022264,,,,,,,,,C0423318,,142500,MONDO:0007722,heterochromia iridis,
+BMGC_DS06508,BMG_DS022271,,,,,,,,,C0423401,,180000,MONDO:0008373,retinal arterial tortuosity,
+BMGC_DS06509,BMG_DS022274,,"Low Back Pain, Mechanical",Low Back Pain,,,,,,C0423682,D017116,,,,
+BMGC_DS06510,BMG_DS022280,,"Neuralgia, Perineal",Neuralgia,,,,,,C0423711,D009437,,,,
+BMGC_DS06511,BMG_DS022281,,"Neuralgia, Iliohypogastric Nerve",Neuralgia,,,,,,C0423712,D009437,,,,
+BMGC_DS06512,BMG_DS022284,48596006;247448009,Scurfiness of scalp,,,,,,,C0423775,,,MONDO:0024343,pityriasis simplex,Pityriasis simplex | Pityriasis streptogenes | Scurfiness of scalp | Dandruff | Scurf | Pityriasis capitis | Pityriasis sicca | Seborrhea capitis | Seborrheic dermatitis of scalp | Seborrheic eczema of scalp | Seborrhea sicca | Seborrhoea capitis | Seborrhoea sicca | Seborrhoeic eczema of scalp | Seborrhoeic dermatitis of scalp | Scurfiness of scalp (disorder) | Scurfiness of scalp | Scurfiness of scalp (finding)
+BMGC_DS06513,BMG_DS022307,,Spastic Quadriplegia,Quadriplegia,,,,,,C0426970,D011782,,MONDO:0016215,spastic quadriplegic cerebral palsy,
+BMGC_DS06514,BMG_DS022309,,Facial Paresis,Facial Paralysis,,,,,,C0427055,D005158,,,,
+BMGC_DS06515,BMG_DS022321,250978003,Aortic valve calcification,,,,,,,C0428791,,MTHU014585,MONDO:0005463,aortic valve calcification,Aortic valve calcification | Calcified aortic valve | Aortic valve calcification (disorder)
+BMGC_DS06516,BMG_DS022328,251047005,Dilatation of pulmonary artery (disorder),,,,,,,C0428851,,,,,Dilatation of pulmonary artery | Dilatation of pulmonary artery (disorder)
+BMGC_DS06517,BMG_DS022329,,,,,,,,,C0428908,,,MONDO:0000469,sinoatrial node disorder,
+BMGC_DS06518,BMG_DS022331,72654001,Supraventricular arrhythmia,,,,,,,C0428974,,,,,Supraventricular arrhythmia | Supraventricular arrhythmia (disorder)
+BMGC_DS06519,BMG_DS022348,,,,,,,,,C0431108,,,MONDO:0016703,anaplastic oligoastrocytoma,
+BMGC_DS06520,BMG_DS022349,,,,,,,DOID:5648,choroid plexus carcinoma,C0431109,,,MONDO:0016718,choroid plexus carcinoma,
+BMGC_DS06521,BMG_DS022352,,,,,,,DOID:4584,choroid plexus meningioma,C0431118,,,MONDO:0003053,choroid plexus meningioma,
+BMGC_DS06522,BMG_DS022353,,,,,,,DOID:4591,lymphoplasmacyte-rich meningioma,C0431119,,,MONDO:0003056,lymphoplasmacyte-rich meningioma,
+BMGC_DS06523,BMG_DS022354,,,,,,,DOID:4210,clear cell meningioma,C0431121,,,MONDO:0002918,clear cell meningioma,
+BMGC_DS06524,BMG_DS022355,,,,,,,DOID:3196,cellular schwannoma,C0431124,,,MONDO:0002548,cellular schwannoma,
+BMGC_DS06525,BMG_DS022356,,,,,,,DOID:3847,papillary craniopharyngioma,C0431128,,,MONDO:0002788,papillary craniopharyngioma,
+BMGC_DS06526,BMG_DS022357,,,,,,,DOID:3846,adamantinous craniopharyngioma,C0431129,,,MONDO:0002787,adamantinous craniopharyngioma,
+BMGC_DS06527,BMG_DS022367,,,,,,,,,C0431349,,,MONDO:0035450,aprosencephaly,
+BMGC_DS06528,BMG_DS022371,,,,,,,,,C0431362,,,MONDO:0019756,lobar holoprosencephaly,
+BMGC_DS06529,BMG_DS022372,,,,,,,,,C0431363,,,MONDO:0019757,alobar holoprosencephaly,
+BMGC_DS06530,BMG_DS022375,,Classical Lissencephaly,Classical Lissencephalies and Subcortical Band Heterotopias,,,,DOID:0060402,chromosome 17p13.1 deletion syndrome,C0431375,D054221,,MONDO:0015146,classic lissencephaly,
+BMGC_DS06531,BMG_DS022377,,,,,,,,,C0431380,,,MONDO:0017094,cerebral cortical dysplasia,
+BMGC_DS06532,BMG_DS022379,,,,,,,,,C0431384,,,MONDO:0022236,colpocephaly,
+BMGC_DS06533,BMG_DS022380,253170008,Hemimegalencephaly,Hemimegalencephaly,,,,,,C0431391,D065705,MTHU037012,MONDO:0020492,hemimegalencephaly,Hemimegalencephaly | Hemimegalencephaly (disorder)
+BMGC_DS06534,BMG_DS022381,156895002;204053001;253175003,Familial aplasia of the vermis,,,,,,,C0431399,,,MONDO:0018772,Joubert syndrome,Familial aplasia of the vermis | Familial aplasia of the vermis (disorder)
+BMGC_DS06535,BMG_DS022383,253176002,Gillespie syndrome,,,,,DOID:0111578,Gillespie syndrome,C0431401,C536370,206700,MONDO:0008795,aniridia-cerebellar ataxia-intellectual disability syndrome,"Gillespie syndrome | Gillespie syndrome (disorder) | Aniridia, cerebellar ataxia, intellectual disability syndrome"
+BMGC_DS06536,BMG_DS022384,51409009,Asymmetric crying face association,,,,,,,C0431406,,125520,MONDO:0007443,congenital unilateral hypoplasia of depressor anguli oris,Asymmetric crying face association | Cardiofacial syndrome | Asymmetric crying face association (disorder) | Asymmetrical crying face syndrome | Asymmetric crying facies | Congenital unilateral hypoplasia of depressor anguli oris
+BMGC_DS06537,BMG_DS022386,,Vein of Galen aneurysm,,,,,,,C0431420,C536535,,MONDO:0015196,vein of Galen aneurysm,
+BMGC_DS06538,BMG_DS022395,8793008,Mayer-Rokitansky-Kuster syndrome,,,,,,,C0431648,,,MONDO:0017771,Mayer-Rokitansky-Kuster-Hauser syndrome,Rokitansky sequence | Mayer-Rokitansky-Kuster syndrome | Rokitansky sequence (disorder) | Congenital absence of uterus and vagina
+BMGC_DS06539,BMG_DS022397,,,,,,,,,C0431692,,,MONDO:0019980,"renal hypoplasia, bilateral",
+BMGC_DS06540,BMG_DS022398,446641003;609572000,Renal cysts and diabetes syndrome,,,,,,,C0431693,C535520,137920,MONDO:0007669,renal cysts and diabetes syndrome,"Renal cysts and diabetes syndrome (disorder) | Renal cysts and diabetes syndrome | Maturity-onset diabetes of the young, type 5 (disorder) | Maturity-onset diabetes of the young, type 5 | MODY5 - maturity-onset diabetes of the young type 5 | Renal cysts and diabetes syndrome | HNF1B-MODY - HNF1 homeobox B maturity-onset diabetes of the young type 5 | HNF1B (HNF1 homeobox B) monogenic diabetes mellitus | HNF1B monogenic diabetes mellitus"
+BMGC_DS06541,BMG_DS022400,,,,,,,,,C0431697,,,MONDO:0019644,"renal dysplasia, unilateral",
+BMGC_DS06542,BMG_DS022401,,,,,,,,,C0431698,,,MONDO:0019645,"renal dysplasia, bilateral",
+BMGC_DS06543,BMG_DS022407,253883006,Multiple renal cysts,,,,,,,C0431718,,MTHU015022,,,Multiple renal cysts | Multiple renal cysts (disorder)
+BMGC_DS06544,BMG_DS022418,,,,,,,,,C0431886,,314100,MONDO:0010746,"thumbs, congenital Clasped",
+BMGC_DS06545,BMG_DS022420,,,,,,,,,C0431904,,,MONDO:0017426,postaxial polydactyly of fingers,
+BMGC_DS06546,BMG_DS022424,,,,,,,,,C0432028,,,MONDO:0017450,split foot,
+BMGC_DS06547,BMG_DS022429,,,,,,,,,C0432090,,,MONDO:0015092,cleft hard palate,
+BMGC_DS06548,BMG_DS022430,,,,,,,,,C0432098,,119570,MONDO:0007338,cleft soft palate,
+BMGC_DS06549,BMG_DS022434,,,,,,,,,C0432122,,190440,MONDO:0008603,trigonocephaly 1,
+BMGC_DS06550,BMG_DS022435,,Kleeblattschaedel syndrome,,,,,,,C0432126,C536884,148800,MONDO:0007861,isolated cloverleaf skull syndrome,
+BMGC_DS06551,BMG_DS022436,,,,,,,,,C0432160,,214290,MONDO:0008957,"cervical vertebrae, agenesis of",
+BMGC_DS06552,BMG_DS022443,254049009,Schneckenbecken dysplasia,,,,,DOID:0050775,schneckenbecken dysplasia,C0432194,C536637,269250,MONDO:0010013,schneckenbecken dysplasia,Schneckenbecken dysplasia | Schneckenbecken dysplasia (disorder)
+BMGC_DS06553,BMG_DS022444,,,,,,,,,C0432195,,,MONDO:0019691,short rib dysplasia,
+BMGC_DS06554,BMG_DS022445,,"Short rib-polydactyly syndrome, Verma-Naumoff type",,,,,,,C0432197,C537602,,,,
+BMGC_DS06555,BMG_DS022446,,"Short rib-polydactyly syndrome, Beemer type",,,,,DOID:9249,Beemer-Langer syndrome,C0432198,C537599,269860,MONDO:0010024,Beemer-Langer syndrome,
+BMGC_DS06556,BMG_DS022447,254054000,Boomerang dysplasia,,,,,DOID:0050680,Boomerang dysplasia,C0432201,C536573,112310,MONDO:0007208,Boomerang dysplasia,Boomerang dysplasia | Boomerang dysplasia (disorder)
+BMGC_DS06557,BMG_DS022448,254058002,Pseudodiastrophic dysplasia,,,,,,,C0432206,C535826,264180,MONDO:0009914,pseudodiastrophic dysplasia,Pseudodiastrophic dysplasia | Pseudodiastrophic dysplasia (disorder)
+BMGC_DS06558,BMG_DS022450,,"Dyssegmental dysplasia, Rolland-Desbuquois type",,,,,,,C0432209,C537999,224400,MONDO:0009139,"dyssegmental dysplasia, Rolland-Desbuquois type",
+BMGC_DS06559,BMG_DS022451,254062008,Spondyloepimetaphyseal disorder,,,,,,,C0432211,,,MONDO:0100510,spondyloepimetaphyseal dysplasia,Spondyloepimetaphyseal disorder | Spondyloepimetaphyseal disorder (disorder) | Spondyloepimetaphyseal dysplasia
+BMGC_DS06560,BMG_DS022452,,"Spondyloepimetaphyseal Dysplasia, Irapa Type",,,,,,,C0432213,C562958,271650,MONDO:0010076,"spondyloepimetaphyseal dysplasia, Irapa type",
+BMGC_DS06561,BMG_DS022453,254064009,Namaqualand hip dysplasia,,,,,,,C0432214,,604864,MONDO:0011496,mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis,Namaqualand hip dysplasia | Namaqualand hip dysplasia (disorder)
+BMGC_DS06562,BMG_DS022454,254065005,Progressive pseudorheumatoid dysplasia,,,,,,,C0432215,C535387,208230,MONDO:0008827,progressive pseudorheumatoid arthropathy of childhood,Progressive pseudorheumatoid dysplasia | Progressive pseudorheumatoid dysplasia (disorder)
+BMGC_DS06563,BMG_DS022455,254066006,Wolcott-Rallison syndrome,,,,,DOID:0090060,Wolcott-Rallison syndrome,C0432217,C536739,226980,MONDO:0009192,Wolcott-Rallison syndrome,"Wolcott-Rallison dysplasia | Wolcott-Rallison syndrome | Epiphyseal dysplasia, multiple, with early onset diabetes mellitus | Wolcott-Rallison dysplasia (disorder)"
+BMGC_DS06564,BMG_DS022457,254068007,Opsismodysplasia,,,,,,,C0432219,C537122,258480,MONDO:0009785,opsismodysplasia,Opsismodysplasia | Opsismodysplasia (disorder)
+BMGC_DS06565,BMG_DS022458,,"Spondylometaphyseal dysplasia, 'corner fracture' type",,,,,DOID:0112297,spondylometaphyseal dysplasia corner fracture type,C0432221,C535793,184255,MONDO:0008479,"spondylometaphyseal dysplasia, 'corner fracture' type",
+BMGC_DS06566,BMG_DS022459,254079002,Spondyloenchondrodysplasia,,,,,,,C0432222,C535782,,,,Spondyloenchondrodysplasia | Spondyloenchondrodysplasia (disorder)
+BMGC_DS06567,BMG_DS022460,,,,,,,,,C0432224,,118651,MONDO:0007322,"chondrodysplasia punctata, tibial-metacarpal type",
+BMGC_DS06568,BMG_DS022461,,Metaphyseal chondrodysplasia Spahr type,,,,,,,C0432225,C537353,250400,MONDO:0009597,"metaphyseal chondrodysplasia, Spahr type",
+BMGC_DS06569,BMG_DS022462,254085009,Metaphyseal anadysplasia,,,,,,,C0432226,C537351,309645,MONDO:0015177,metaphyseal anadysplasia,Metaphyseal anadysplasia | Metaphyseal anadysplasia (disorder)
+BMGC_DS06570,BMG_DS022463,,,,,,,,,C0432227,,113500,MONDO:0007232,autosomal dominant brachyolmia,
+BMGC_DS06571,BMG_DS022464,254088006,Brachyolmia,,,,,DOID:0050690,brachyolmia,C0432228,C537098,,MONDO:0015262,brachyolmia,Brachyolmia | Brachyolmia (disorder)
+BMGC_DS06572,BMG_DS022466,,,,,,,,,C0432230,,249700,MONDO:0009588,Langer mesomelic dysplasia,
+BMGC_DS06573,BMG_DS022467,33979003,Nievergelt syndrome,,,,,,,C0432231,C536120,163400,MONDO:0008098,"mesomelic dwarfism, Nievergelt type",Nievergelt's syndrome | Nievergelt-Erb syndrome | Mesomelic dysplasia - Nievergelt type | Nievergelt's syndrome (disorder) | Nievergelt syndrome
+BMGC_DS06574,BMG_DS022468,239016009;254091006,Trichorhinophalangeal dysplasia type I,,,,,DOID:14743,trichorhinophalangeal syndrome type I,C0432233,,190350,MONDO:0008596,trichorhinophalangeal syndrome type I,Trichorhinophalangeal dysplasia type I | Trichorhinophalangeal dysplasia type I (disorder) | Trichorhinophalangeal dysplasia type I | Trichorhinophalangeal syndrome I | TRPS I - Trichorhinophalangeal syndrome I | Trichorhinophalangeal dysplasia type I (disorder)
+BMGC_DS06575,BMG_DS022469,,CRANIOECTODERMAL DYSPLASIA 1,,,,,DOID:0080803,cranioectodermal dysplasia 1,C0432235,,606045;218330,MONDO:0021093,cranioectodermal dysplasia 1,
+BMGC_DS06576,BMG_DS022470,,,,,,,,,C0432238,,,MONDO:0019698,bent bone dysplasia,
+BMGC_DS06577,BMG_DS022471,254096001,Kyphomelic dysplasia,,,,,,,C0432239,C538128,211350,MONDO:0008881,kyphomelic dysplasia,Kyphomelic dysplasia | Kyphomelic dysplasia (disorder)
+BMGC_DS06578,BMG_DS022472,254099008,Desbuquois syndrome,,,,,DOID:0060462,Desbuquois dysplasia,C0432242,C535943,,MONDO:0015426,Desbuquois dysplasia,Desbuquois syndrome | Desbuquois syndrome (disorder) | Desbuquois dysplasia
+BMGC_DS06579,BMG_DS022473,,Spondyloepimetaphyseal Dysplasia With Joint Laxity,,,,,DOID:0112197,spondyloepimetaphyseal dysplasia with joint laxity,C0432243,C562968,,MONDO:0019675,spondyloepimetaphyseal dysplasia with joint laxity,
+BMGC_DS06580,BMG_DS022475,,"Microcephalic Osteodysplastic Primordial Dwarfism, Type II",,,,,DOID:0060609,microcephalic osteodysplastic primordial dwarfism type II,C0432246,C565898,210720,MONDO:0008872,microcephalic osteodysplastic primordial dwarfism type II,
+BMGC_DS06581,BMG_DS022476,254112001,Osteoporosis with pseudoglioma,,,,,DOID:0060849,osteoporosis-pseudoglioma syndrome,C0432252,,259770,MONDO:0009820,osteoporosis-pseudoglioma syndrome,Osteoporosis with pseudoglioma | Osteoporosis with pseudoglioma (disorder)
+BMGC_DS06582,BMG_DS022477,254113006,Bruck syndrome,,,,,,,C0432253,,,MONDO:0017195,Bruck syndrome,Bruck syndrome | Bruck syndrome (disorder)
+BMGC_DS06583,BMG_DS022478,,Singleton Merten syndrome,,,,,,,C0432254,C537343,,MONDO:0008429,Singleton-Merten dysplasia,
+BMGC_DS06584,BMG_DS022479,254116003,Geroderma osteodysplastica,,,,,DOID:0111266,geroderma osteodysplasticum,C0432255,C537799,231070,MONDO:0009271,geroderma osteodysplastica,Geroderma osteodysplastica | Osteodysplastic geroderma | GO - Geroderma osteodysplastica | Geroderma osteodysplastica (disorder)
+BMGC_DS06585,BMG_DS022483,254121000,Osteopetrosis - intermediate type,,,,,,,C0432261,,,,,Osteopetrosis - intermediate type | Osteopetrosis - intermediate type (disorder)
+BMGC_DS06586,BMG_DS022484,254123002,Dysosteosclerosis,,,,,,,C0432262,C562973,224300;MTHU064939,MONDO:0009138,dysosteosclerosis,Dysosteosclerosis | Dysosteosclerosis (disorder)
+BMGC_DS06587,BMG_DS022486,254125009,Axial osteosclerosis,,,,,,,C0432264,C537792,166450,MONDO:0008155,osteomesopyknosis,Axial osteosclerosis | Axial osteosclerosis (disorder) | Osteomesopycnosis
+BMGC_DS06588,BMG_DS022487,,IBIDS Syndrome,Trichothiodystrophy Syndromes,,,,DOID:0111868;DOID:2960,photosensitive trichothiodystrophy | nonphotosensitive trichothiodystrophy 5,C0432267,D054463,,,,
+BMGC_DS06589,BMG_DS022488,,Osteopathia striata cranial sclerosis,,,,,DOID:0060886,osteopathia striata with cranial sclerosis,C0432268,C536053,300373,MONDO:0010310,osteopathia striata with cranial sclerosis,
+BMGC_DS06590,BMG_DS022489,,,,,,,DOID:0111507,Lenz-Majewski hyperostotic dwarfism,C0432269,,151050,MONDO:0007892,Lenz-Majewski hyperostotic dwarfism,
+BMGC_DS06591,BMG_DS022491,59763006,Van Buchem disease,,,,,,,C0432272,,239100,MONDO:0009395,hyperostosis corticalis generalisata,Hyperphosphatasemia tarda | Hyperostosis corticalis generalisata | Leontiasis ossea generalisata | Hyperphosphatasia tarda | van Buchem's syndrome | Van Buchem disease | Hyperphosphatasaemia tarda | Hyperphosphatasemia tarda (disorder)
+BMGC_DS06592,BMG_DS022492,254131007,Worth disease,,,,,DOID:0080037,Worth syndrome,C0432273,,144750;607636,MONDO:0007764,"autosomal dominant osteosclerosis, Worth type",Autosomal dominant osteosclerosis | Worth disease | Worth disease (disorder)
+BMGC_DS06593,BMG_DS022495,240187003;205480005,Dysplasia epiphysealis hemimelica,,,,,,,C0432282,C537997,127800,MONDO:0007489,dysplasia epiphysealis hemimelica,Dysplasia epiphysealis hemimelica | Dysplasia epiphysealis hemimelica (disorder) | Dysplasia epiphysealis hemimelica | Dysplasia epiphysealis hemimelica (disorder) | Trevor disease | Trevor's disease
+BMGC_DS06594,BMG_DS022496,,,,,,,DOID:0111532,osteoglophonic dysplasia,C0432283,,166250,MONDO:0008150,osteoglophonic dwarfism,
+BMGC_DS06595,BMG_DS022497,,,,,,,,,C0432284,,,MONDO:0016824,infantile myofibromatosis,
+BMGC_DS06596,BMG_DS022499,,Dermochondrocorneal dystrophy of François,,,,,,,C0432288,C535375,221800,MONDO:0009094,dermochondrocorneal dystrophy,
+BMGC_DS06597,BMG_DS022500,254151006,Winchester syndrome (disorder),,,,,,,C0432289,,277950,MONDO:0010201,Winchester syndrome,Winchester syndrome | Winchester syndrome (disorder)
+BMGC_DS06598,BMG_DS022501,109419009,Mandibuloacral dysostosis,,,,,,,C0432291,,,MONDO:0016584,mandibuloacral dysplasia,Mandibuloacral dysostosis | Mandibuloacral dysostosis (disorder) | Mandibuloacral dysplasia | Familial mandibuloacral dysplasia | Craniomandibular dermatodysostosis
+BMGC_DS06599,BMG_DS022502,,,,,,,DOID:0111542,familial expansile osteolysis,C0432292,,174810,MONDO:0008275,familial expansile osteolysis,
+BMGC_DS06600,BMG_DS022504,,,,,,,,,C0432300,,146700,MONDO:0007810,autosomal dominant ichthyosis vulgaris,
+BMGC_DS06601,BMG_DS022506,,"Lamellar ichthyosis, autosomal dominant form",,,,,,,C0432304,C537263,146750,MONDO:0007812,"ichthyosis, lamellar, autosomal dominant",
+BMGC_DS06602,BMG_DS022507,,,,,,,DOID:0060877,bullous congenital ichthyosiform erythroderma,C0432306,,146800,MONDO:0007813,superficial epidermolytic ichthyosis,
+BMGC_DS06603,BMG_DS022509,,,,,,,,,C0432311,,146600,MONDO:0007809,"ichthyosis histrix, Lambert type",
+BMGC_DS06604,BMG_DS022512,,,,,,,DOID:0111346,epidermolysis bullosa simplex with mottled pigmentation,C0432316,,131960,MONDO:0007556,"epidermolysis bullosa simplex 2F, with mottled pigmentation",
+BMGC_DS06605,BMG_DS022513,60518002;398071000,"Epidermolysis bullosa simplex, Ogna type",,,,,,,C0432317,C535962,131950,MONDO:0007555,"pidermolysis bullosa simplex 5A, Ogna type","Autosomal dominant epidermolysis bullosa simplex | EBS 1 | Epidermolysis bullosa simplex, Ogna type | Epidermolysis bullosa simplex of Ogna | Autosomal dominant epidermolysis bullosa simplex (disorder) | Epidermolysis bullosa simplex, Ogna type (disorder) | Epidermolysis bullosa simplex, Ogna type | Epidermolysis bullosa simplex of Ogna"
+BMGC_DS06606,BMG_DS022515,,,,,,,,,C0432321,,131850,MONDO:0007552,pretibial dystrophic epidermolysis bullosa,
+BMGC_DS06607,BMG_DS022516,,,,,,,,,C0432322,,131750,MONDO:0007549,generalized dominant dystrophic epidermolysis bullosa,
+BMGC_DS06608,BMG_DS022518,254196004,Junctional epidermolysis bullosa mitis,,,,,,,C0432326,,,MONDO:0019307,generalized junctional epidermolysis bullosa non-Herlitz type,Junctional epidermolysis bullosa mitis | Junctional epidermolysis bullosa mitis (disorder) | Generalized atrophic benign epidermolysis bullosa - GABEB | Generalised atrophic benign epidermolysis bullosa - GABEB | Junctional epidermolysis bullosa generalized intermediate | Junctional epidermolysis bullosa generalised intermediate | Generalised junctional epidermolysis bullosa non-Herlitz type | Generalized junctional epidermolysis bullosa non-Herlitz type | Junctional epidermolysis bullosa Disentis type
+BMGC_DS06609,BMG_DS022522,,Cutis Laxa-Marfanoid Syndrome,,,,,,,C0432335,C563639,614100,MONDO:0013574,cutis laxa - Marfanoid syndrome,
+BMGC_DS06610,BMG_DS022523,,,,,,,DOID:0070144,autosomal recessive cutis laxa type I,C0432336,,,,,
+BMGC_DS06611,BMG_DS022528,254232009;254230001,Uncombable hair syndrome,,,,,,,C0432347,C536939,,MONDO:0008621,uncombable hair syndrome,Uncombable hair syndrome | Uncombable hair syndrome (disorder) | Uncombable hair syndrome | Spun glass hair | Pili trianguli et canaliculi | Uncombable hair syndrome (disorder)
+BMGC_DS06612,BMG_DS022530,,,,,,,,,C0432357,,,MONDO:0015855,isolated congenital breast hypoplasia/aplasia,
+BMGC_DS06613,BMG_DS022531,,Isotretinoin embryopathy like syndrome,,,,,,,C0432364,C535542,243440,MONDO:0009473,isotretinoin-like syndrome,
+BMGC_DS06614,BMG_DS022551,,"Down Syndrome, Partial Trisomy 21",Down Syndrome,,,,,,C0432416,D004314,,,,
+BMGC_DS06615,BMG_DS022552,,"Trisomy 21, Meiotic Nondisjunction",Down Syndrome,,,,,,C0432417,D004314,,,,
+BMGC_DS06616,BMG_DS022568,,Chromosome 18p deletion syndrome,,,,,DOID:0060406,chromosome 18p deletion syndrome,C0432442,C538309,146390,MONDO:0007800,chromosome 18p deletion syndrome,
+BMGC_DS06617,BMG_DS022569,205631008;270889005,Deletion of long arm of chromosome 18,,,,,,,C0432443,,601808,MONDO:0011147,chromosome 18q deletion syndrome,Deletion of arm of chromosome 18: [long] or [p] | 18p- syndrome | Deletion of long arm of chromosome 18 | Deletion of arm of chromosome 18: [long] or [p] (disorder) | Deletion of long arm of chromosome 18 | 18q- syndrome | Deletion of long arm of chromosome 18 (disorder)
+BMGC_DS06618,BMG_DS022593,,,,,,,,,C0432487,,,MONDO:0019088,post-transplant lymphoproliferative disease,
+BMGC_DS06619,BMG_DS022594,,,,,,,DOID:8883,lower lip cancer,C0432520,,,MONDO:0004673,lower lip cancer,
+BMGC_DS06620,BMG_DS022596,35548007;1295239009;254737002,Proliferative fasciitis,,,,,DOID:9599,proliferative fasciitis,C0432528,,,MONDO:0004831,proliferative fasciitis,Nodular fasciitis | Pseudosarcomatous fibromatosis | Pseudosarcomatous fasciitis | Proliferative fasciitis | Infiltrative fasciitis | Nodular fasciitis (disorder) | Proliferative fasciitis (morphologic abnormality) | Proliferative fasciitis | Proliferative fasciitis | Proliferative fasciitis (disorder)
+BMGC_DS06621,BMG_DS022597,254738007,Intravascular fasciitis,,,,,DOID:9603,intravascular fasciitis,C0432529,,,MONDO:0004836,intravascular fasciitis,Intravascular fasciitis | Intravascular fasciitis (disorder)
+BMGC_DS06622,BMG_DS022598,,,,,,,DOID:8630,upper lip cancer,C0432579,,,,,
+BMGC_DS06623,BMG_DS022599,,,,,,,DOID:9125,lower gum cancer,C0432581,,,MONDO:0004713,lower gum cancer,
+BMGC_DS06624,BMG_DS022629,50390006,Non-specific granulomatous orchitis,,,,,DOID:3089,granulomatous orchitis,C0436545,,,MONDO:0002509,non-specific granulomatous orchitis,Non-specific granulomatous orchitis | Non-specific granulomatous orchitis (disorder) | Granulomatous orchitis
+BMGC_DS06625,BMG_DS022631,,Myoclonic Encephalopathy,"Epilepsies, Myoclonic",,,,,,C0438414,D004831,,,,
+BMGC_DS06626,BMG_DS022646,,,,,,,DOID:9973,substance dependence,C0439857,,,,,
+BMGC_DS06627,BMG_DS022651,386033004;264554005;277878001;42658009;277317008;193167000,Neuropathy,,,,,DOID:870,neuropathy,C0442874,,MTHU016030,,,Neuropathy (disorder) | Neuropathy | Neuropathy (nerve damage) | Neuropathy | PN - Peripheral neuropathy | Peripheral neuropathy | Neuropathy (disorder) | Neuropathy | Neuropathy (disorder) | Disorder of the peripheral nervous system | Disorder of the peripheral nervous system (disorder)
+BMGC_DS06628,BMG_DS022658,95566004;198527007,Urolithiasis,Urolithiasis,,,,DOID:0080653,urolithiasis,C0451641,D052878,MTHU014570,MONDO:0024647,urolithiasis,Urolithiasis | Urolithiasis (disorder) | Urinary calculus | Urinary stone | Urolith in urinary system | Urolithiasis | Urolithiasis (disorder)
+BMGC_DS06629,BMG_DS022664,193165008,Neuropathy in association with hereditary ataxia,,8A03.15,Ataxia due to mitochondrial mutations,G60.2,DOID:0090115,spinocerebellar ataxia with axonal neuropathy 1,C0451669,,,,,Neuropathy in association with hereditary ataxia | Neuropathy in association with hereditary ataxia (disorder)
+BMGC_DS06630,BMG_DS022674,,Posterior Cerebral Artery Syndrome,"Infarction, Posterior Cerebral Artery",,,,,,C0451681,D020762,,,,
+BMGC_DS06631,BMG_DS022686,191008001,Immunodeficiency following hereditary defective response to Epstein-Barr virus,,4A01.22,Immune dysregulation syndromes presenting primarily with lymphoproliferation,D82.3,DOID:0060706;DOID:0060705,X-linked lymphoproliferative syndrome 1 | X-linked lymphoproliferative syndrome 2,C0451697,,,,,Immunodeficiency following hereditary defective response to Epstein-Barr virus | Immunodeficiency following hereditary defective response to Epstein-Barr virus (disorder)
+BMGC_DS06632,BMG_DS022704,197594005,"Nephrotic syndrome, focal and segmental glomerular lesions",,,,,,,C0451720,,,,,"Nephrotic syndrome, focal and segmental glomerular lesions | Nephrotic syndrome, focal and segmental glomerular lesions (disorder)"
+BMGC_DS06633,BMG_DS022818,194417009,"Conductive hearing loss, bilateral",,AB51.0,Acquired conductive hearing loss,H90.0,,,C0452136,,MTHU046055,,,"Conductive hearing loss, bilateral | Conductive hearing loss, bilateral (disorder)"
+BMGC_DS06634,BMG_DS022820,194424005,Sensorineural hearing loss of bilateral ears,,,,,,,C0452138,,,,,Sensorineural hearing loss of bilateral ears | Sensorineural hearing loss of both ears | Sensorineural hearing loss of bilateral ears (disorder)
+BMGC_DS06635,BMG_DS022856,,,,,,,DOID:0060243,stuttering,C0454542,,,,,
+BMGC_DS06636,BMG_DS022882,,Oral Dyskinesia,Dyskinesias,,,,,,C0454606,D020820,,,,
+BMGC_DS06637,BMG_DS022901,229734008,Expressive language delay,,,,,,,C0454641,,MTHU018110,,,Expressive language delay | Expressive language delay (disorder) | Developmental expressive language delay | Expressive developmental language delay
+BMGC_DS06638,BMG_DS022905,,Benedict Syndrome,Brain Stem Infarctions,,,,,,C0455715,D020526,,,,
+BMGC_DS06639,BMG_DS022906,,Foville Syndrome,Brain Stem Infarctions,,,,,,C0455716,D020526,,,,
+BMGC_DS06640,BMG_DS022907,,Weber Syndrome,Brain Stem Infarctions,,,,,,C0455717,D020526,,MONDO:0023642,Weber syndrome,
+BMGC_DS06641,BMG_DS022908,,Top of the Basilar Syndrome,Brain Stem Infarctions,,,,,,C0455718,D020526,,,,
+BMGC_DS06642,BMG_DS022918,,"Hydrops Fetalis, Non-Immune",Hydrops Fetalis,,,,,,C0455988,D015160,236750,MONDO:0009369,non-immune hydrops fetalis,
+BMGC_DS06643,BMG_DS022919,,Immune Hydrops Fetalis,Hydrops Fetalis,,,,,,C0455990,D015160,,MONDO:0018221,immune hydrops fetalis,
+BMGC_DS06644,BMG_DS022974,206376005,Sepsis of the newborn,,,,,,,C0456103,,,MONDO:0700217,neonatal sepsis,Sepsis of the newborn | Sepsis of the newborn (disorder)
+BMGC_DS06645,BMG_DS022977,276674008,Neonatal meningitis,,,,,,,C0456107,,,,,Neonatal meningitis | Neonatal meningitis (disorder)
+BMGC_DS06646,BMG_DS022991,276703007,Osteopenia of prematurity,,,,,,,C0456127,,,,,Osteopenia of prematurity | Osteopenic rickets | Osteopenia of prematurity (disorder)
+BMGC_DS06647,BMG_DS022996,,Simple Endometrial Hyperplasia,Endometrial Hyperplasia,,,,DOID:0080365,endometrial hyperplasia,C0456483,D004714,,MONDO:0006410;MONDO:0041161,simple endometrial hyperplasia | obsolete endometrial hyperplasia,
+BMGC_DS06648,BMG_DS022997,,,,,,,DOID:3852,Peutz-Jeghers syndrome,C0456487,,,MONDO:0006365,Peutz-Jeghers polyp,
+BMGC_DS06649,BMG_DS023001,,"Median Neuropathy, Proximal",Median Neuropathy,,,,,,C0456516,D020423,,,,
+BMGC_DS06650,BMG_DS023015,,,,,,,DOID:9547,non-secretory myeloma,C0456845,,,,,
+BMGC_DS06651,BMG_DS023017,,,,,,,,,C0456889,,,MONDO:0019473,enteropathy-associated T-cell lymphoma,
+BMGC_DS06652,BMG_DS023018,,,,,,,,,C0456891,,265430,MONDO:0009936,familial primary pulmonary hypoplasia,
+BMGC_DS06653,BMG_DS023019,139548004;40031005,Blindness,Blindness,,,,,,C0456909,D001766,MTHU001370,MONDO:0001941,blindness (disorder),Blindness | Blindness (finding) | Low vision | Visual loss | Decreased vision | Vision problem | Abnormal vision | Can't see properly | Impaired vision | Loss of vision | Partial sight | Problem seeing | Visual impairment | Visual disorder | Unable to see | UTS - Unable to see | Sight impaired | Reduced ability to see | Problem sight | Poor vision | LV - Low vision | Difficulty seeing | Cannot see properly | Cannot see | Vision problem (disorder)
+BMGC_DS06654,BMG_DS023027,277807007,Weyers acrofacial dysostosis,,,,,DOID:0111571,Weyers acrofacial dysostosis,C0457013,C536695,193530,MONDO:0008673,"acrofacial dysostosis, Weyers type",Curry-Hall syndrome | Curry-Hall syndrome (disorder) | Acrofacial dysostosis Weyers type | Weyers acrofacial dysostosis | Weyers acrodental dysostosis
+BMGC_DS06655,BMG_DS023030,277950001,Muscle eye brain disease,,,,,,,C0457133,,,MONDO:0018939,muscle-eye-brain disease,Muscle eye brain disease | Muscle eye brain disease (disorder)
+BMGC_DS06656,BMG_DS023060,,Complex Regional Pain Syndromes,Complex Regional Pain Syndromes,,,,DOID:3223,complex regional pain syndrome,C0458219,D020918,,MONDO:0019369,complex regional pain syndrome,
+BMGC_DS06657,BMG_DS023108,230686005,Generalized myasthenia,,,,,,,C0472367,,,,,Generalised myasthenia | Generalized myasthenia | Generalized myasthenia (disorder)
+BMGC_DS06658,BMG_DS023109,230706003,Hemorrhagic cerebral infarction,,,,,,,C0472369,,,,,Hemorrhagic cerebral infarction | Haemorrhagic cerebral infarction | Hemorrhagic cerebral infarction (disorder)
+BMGC_DS06659,BMG_DS023112,,Posterior Circulation Transient Ischemic Attack,"Ischemic Attack, Transient",,,,,,C0472381,D002546,,,,
+BMGC_DS06660,BMG_DS023127,,,,,,,,,C0472694,,140850,MONDO:0007706,cavernous hemangiomas of face-supraumbilical midline raphe syndrome,
+BMGC_DS06661,BMG_DS023138,234348004,Anemia of renal disease,,,,,,,C0472713,,,,,Anaemia of renal disease | Anemia of renal disease | Anemia of renal disease (disorder) | Nephrogenic anemia | Nephrogenic anaemia
+BMGC_DS06662,BMG_DS023171,191187006,Alpha trait thalassemia,,,,,,,C0472762,,,,,Alpha trait thalassemia | Alpha trait thalassaemia | Alpha trait thalassemia (disorder) | Alpha thalassaemia trait | Alpha thalassemia trait
+BMGC_DS06663,BMG_DS023175,191189009,Beta thalassemia intermedia,,,,,,,C0472767,,,MONDO:0016487,beta-thalassemia intermedia,Beta thalassemia intermedia | Beta thalassaemia intermedia | Beta thalassemia intermedia (disorder)
+BMGC_DS06664,BMG_DS023181,234392002,Hemoglobin E/beta thalassemia disease,,,,,,,C0472777,,,MONDO:0016491,hemoglobin E-beta-thalassemia syndrome,Hemoglobin E/beta thalassemia disease | Double heterozygous for Hb E and beta thalassaemia | Haemoglobin E/beta thalassaemia disease | Double heterozygous for Hb E and beta thalassemia | Hemoglobin E/beta thalassemia disease (disorder)
+BMGC_DS06665,BMG_DS023193,191177007,Hemolytic anemia due to hexokinase deficiency,,,,,,,C0472792,,,,,Hemolytic anemia due to hexokinase deficiency | Haemolytic anaemia due to hexokinase deficiency | Hemolytic anemia due to hexokinase deficiency (disorder)
+BMGC_DS06666,BMG_DS023202,234458004,Hypodysfibrinogenemia,,,,,,,C0472803,,,,,Hypodysfibrinogenaemia | Hypodysfibrinogenemia | Hypodysfibrinogenemia (disorder)
+BMGC_DS06667,BMG_DS023209,234533006,X-linked agammaglobulinemia with growth hormone deficiency,,,,,,,C0472813,,307200,MONDO:0010615,isolated growth hormone deficiency type III,X-linked agammaglobulinemia with growth hormone deficiency | Fleisher syndrome | X-linked agammaglobulinaemia with growth hormone deficiency | X-linked agammaglobulinemia with growth hormone deficiency (disorder) | Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinaemia | Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
+BMGC_DS06668,BMG_DS023212,,WHIM syndrome,,,,,DOID:0060591,WHIM syndrome 1,C0472817,C536697,,MONDO:0023880,WHIM syndrome,
+BMGC_DS06669,BMG_DS023236,,Renal hypouricemia,,,,,,,C0473219,C537757,220150,MONDO:0020728,"hypouricemia, renal 1",
+BMGC_DS06670,BMG_DS023298,,Hypoalphalipoproteinemias,Hypoalphalipoproteinemias,,,,,,C0473527,D052456,,,,
+BMGC_DS06671,BMG_DS023307,238694002,Vibratory angioedema,,,,,,,C0473546,C536347,193050;125630,MONDO:0007447;MONDO:0034556,vibratory angioedema | autosomal dominant vibratory urticaria,Vibratory angio-oedema | Vibratory angioedema (disorder) | Vibratory angioedema
+BMGC_DS06672,BMG_DS023322,,,,,,,DOID:6687,Achenbach syndrome,C0473563,,,MONDO:0006520,Achenbach syndrome,
+BMGC_DS06673,BMG_DS023328,,,,,,,,,C0473579,,,MONDO:0015635,porokeratotic eccrine ostial and dermal duct nevus,
+BMGC_DS06674,BMG_DS023330,,Michelin tire baby syndrome,,,,,,,C0473586,C537575,,MONDO:0007990,multiple benign circumferential skin creases on limbs,
+BMGC_DS06675,BMG_DS023406,87194000,Nerve fiber bundle defect,,,,,DOID:5678,nerve fibre bundle defect,C0474334,,,,,Nerve fiber bundle defect | Nerve fibre bundle defect | Nerve fiber bundle defect (disorder)
+BMGC_DS06676,BMG_DS023411,,Optic Disc Neovascularization,Retinal Neovascularization,,,,,,C0474354,D015861,,,,
+BMGC_DS06677,BMG_DS023418,49362009,Corneal edema caused by wearing of contact lenses,,,,,DOID:11034,contact lens corneal edema,C0474442,,,MONDO:0001183,contact lens corneal edema,Contact lens corneal oedema | Contact lens-induced central corneal oedema | Contact lens corneal edema | Contact lens-induced central corneal edema | Corneal edema caused by wearing of contact lenses (disorder) | Corneal oedema caused by wearing of contact lenses | Corneal edema caused by wearing of contact lenses | Corneal oedema caused by contact lens | Corneal edema caused by contact lens
+BMGC_DS06678,BMG_DS023421,,,,,,,DOID:3001,female reproductive endometrioid cancer,C0474809,,,MONDO:0002480,endometrioid tumor,
+BMGC_DS06679,BMG_DS023427,,,,,,,DOID:6345,malignant melanocytic neoplasm of the peripheral nerve sheath,C0474847,,,MONDO:0003863,malignant melanocytic neoplasm of the peripheral nerve sheath,
+BMGC_DS06680,BMG_DS023429,,,,,,,DOID:8630,upper lip cancer,C0474962,,,,,
+BMGC_DS06681,BMG_DS023430,,,,,,,DOID:8649,tongue cancer,C0474963,,,,,
+BMGC_DS06682,BMG_DS023433,,,,,,,DOID:3148,dermal unilateral segmental cavernous angioma,C0474966,,,MONDO:0002526,dermal unilateral segmental cavernous angioma,
+BMGC_DS06683,BMG_DS023495,277905003,Disorder of keratinization,,,,,,,C0475811,,,MONDO:0045011,keratinization disease,Disorder of keratinisation | Disorder of keratinization | Disorder of keratinization (disorder)
+BMGC_DS06684,BMG_DS023496,277918006,Alpha thalassaemia-mental retardation syndrome,,,,,,,C0475813,,,,,Alpha thalassaemia-mental retardation syndrome | Alpha thalassemia-mental retardation syndrome | Alpha thalassemia-mental retardation syndrome (disorder)
+BMGC_DS06685,BMG_DS023498,,,,,,,DOID:2871,endometrial carcinoma,C0476089,,,MONDO:0002447,endometrial carcinoma,
+BMGC_DS06686,BMG_DS023499,,,,,,,DOID:6214,ovarian papillary neoplasm,C0476121,,,MONDO:0003813,ovarian papillary tumor,
+BMGC_DS06687,BMG_DS023501,,,,,,,DOID:3850,hemangiopericytic tumor,C0476144,,,MONDO:0002789,hemangiopericytic tumor,
+BMGC_DS06688,BMG_DS023503,,,,,,,DOID:315,synovium neoplasm,C0476203,,,MONDO:0002528,synovium neoplasm,
+BMGC_DS06689,BMG_DS023504,,,,,,,DOID:4428,dyslexia,C0476254,,,MONDO:0005489,dyslexia,
+BMGC_DS06690,BMG_DS023505,,,,,,,,,C0476287,,607578,MONDO:0011861,breath-holding Spells,
+BMGC_DS06691,BMG_DS023521,,Other specified coagulation defects,,3B4Z,"Coagulation defects, unspecified",D68.8,DOID:0060601,alpha-2-plasmin inhibitor deficiency,C0477316,,,,,
+BMGC_DS06692,BMG_DS023522,,Other primary thrombocytopenia,,3B64.Z,"Thrombocytopenia, unspecified",D69.4;D69.49,DOID:8925;DOID:0060691;DOID:0090102;DOID:0060651;DOID:0111048;DOID:8925,autosomal dominant isolated macrothrombocytopenia 1 | primary thrombocytopenia | platelet-type bleeding disorder 16 | MYH-9 related disease | platelet-type bleeding disorder 19 | primary thrombocytopenia,C0477317,,,,,
+BMGC_DS06693,BMG_DS023523,,Other specified disorders of white blood cells,,4B0Z,"Immune system disorders involving white cell lineages, unspecified",D72.8;D72.89,DOID:0110117,autoimmune lymphoproliferative syndrome type 4,C0477318,,,,,
+BMGC_DS06694,BMG_DS023528,,Other combined immunodeficiencies,,4A01.1Z,"Combined immunodeficiencies, unspecified",D81.8;D81.89,DOID:0060010,Omenn syndrome,C0477324,,,,,
+BMGC_DS06695,BMG_DS023545,,,,,,,DOID:13839,extrapyramidal and movement disease,C0477355,,,MONDO:0001815,extrapyramidal and movement disease,
+BMGC_DS06696,BMG_DS023549,,Other dystonia,,8A02.Y,Other specified dystonic disorders,G24.8,DOID:0090052;DOID:0090051;DOID:0090053;DOID:0090049,dystonia 23 | dystonia 24 | episodic kinesigenic dyskinesia 1 | paroxysmal nonkinesigenic dyskinesia 1,C0477360,,,,,
+BMGC_DS06697,BMG_DS023550,,Other specified extrapyramidal and movement disorders,,8A0Z,"Movement disorders, unspecified",G25.8;G25.89,DOID:0060697;DOID:0060698,hyperekplexia 2 | hyperekplexia 3,C0477362,,,,,
+BMGC_DS06698,BMG_DS023552,,Other specified degenerative diseases of nervous system,,8A2Z,"Disorders with neurocognitive impairment as a major feature, unspecified",G31.8;G31.89,DOID:0050629,Aicardi-Goutieres syndrome,C0477365,,,,,
+BMGC_DS06699,BMG_DS023558,193037008,Other forms of migraine,,,,,DOID:0060178,familial hemiplegic migraine,C0477373,,,,,Other forms of migraine | Other forms of migraine (disorder)
+BMGC_DS06700,BMG_DS023566,,Other hereditary and idiopathic neuropathies,,8C4Z,"Disorders of nerve root, plexus or peripheral nerves, unspecified",G60.8,DOID:0070158;DOID:0070149;DOID:0070151,hereditary sensory and autonomic neuropathy type 6 | hereditary sensory and autonomic neuropathy type 7 | hereditary sensory neuropathy type 1E,C0477392,,,,,
+BMGC_DS06701,BMG_DS023591,,Post-Traumatic Hydrocephalus,Hydrocephalus,,,,,,C0477432,D006849,,,,
+BMGC_DS06702,BMG_DS023656,,Other chondrocalcinosis,,FA26.2,Chondrocalcinosis,M11.2,DOID:0111063,hyperphosphatemic familial tumoral calcinosis,C0477548,,,,,
+BMGC_DS06703,BMG_DS023744,,Other chronic tubulo-interstitial nephritis,,GB55.Z,"Chronic tubulointerstitial nephritis, unspecified",N11.8,DOID:0060911,karyomegalic interstitial nephritis,C0477729,,,,,
+BMGC_DS06704,BMG_DS023761,,Other specified urinary incontinence,,,,N39.4;N39.49;N39.498,,,C0477757,,,,,
+BMGC_DS06705,BMG_DS023815,,Other congenital ichthyosis,,EC20.Y,Other specified genetic disorders of keratinisation,Q80.8,DOID:0060871;DOID:0060720,autosomal dominant keratitis-ichthyosis-deafness syndrome | autosomal recessive congenital ichthyosis 11,C0478084,,,,,
+BMGC_DS06706,BMG_DS023817,,Other congenital malformation syndromes with other skeletal changes,,LB9Z,"Structural developmental anomalies of the skeleton, unspecified",Q87.5,DOID:0110097;DOID:0060179,short-rib thoracic dysplasia 9 with or without polydactyly | Renpenning syndrome,C0478093,,,,,
+BMGC_DS06707,BMG_DS023831,,,,,,,DOID:8481,rheumatic myocarditis,C0489959,,,,,
+BMGC_DS06708,BMG_DS023834,9009001,Low compliance bladder,,,,,DOID:12144,low compliance bladder,C0489967,,,MONDO:0001446,low compliance bladder,Low compliance bladder | Hypertonic bladder | Low compliance urinary bladder | Low compliance urinary bladder (disorder)
+BMGC_DS06709,BMG_DS023844,78576009;428174001,Infection due to Brucella canis,,,,,DOID:14019,Brucella canis brucellosis,C0494040,,,MONDO:0001857,Brucella canis brucellosis,Canine brucellosis | Infection due to Brucella canis | Canine abortion syndrome | Canine brucellosis (disorder) | Brucella canis infection | Infection caused by Brucella canis | Infection caused by Brucella canis (disorder)
+BMGC_DS06710,BMG_DS023889,,,,,,,DOID:263,kidney cancer,C0494158,,,,,
+BMGC_DS06711,BMG_DS023892,,Other nutritional anemias,,,,D53,,,C0494219,,,,,
+BMGC_DS06712,BMG_DS023899,,Other hereditary hemolytic anemias,,,,D58,,,C0494230,,,,,
+BMGC_DS06713,BMG_DS023910,,Other specified immunodeficiencies,,4B4Z,"Diseases of the immune system, unspecified",D84.8,DOID:0090009;DOID:0090007;DOID:0090010;DOID:0090008;DOID:0090011,immunodeficiency-centromeric instability-facial anomalies syndrome | immunodeficiency-centromeric instability-facial anomalies syndrome 1 | immunodeficiency-centromeric instability-facial anomalies syndrome 4 | immunodeficiency-centromeric instability-facial anomalies syndrome 2 | immunodeficiency-centromeric instability-facial anomalies syndrome 3,C0494266,,,,,
+BMGC_DS06714,BMG_DS023913,,Other hypothyroidism,,,,E03,,,C0494271,,,,,
+BMGC_DS06715,BMG_DS023919,,Hyperparathyroidism and other disorders of parathyroid gland,,,,E21,,,C0494304,,,,,
+BMGC_DS06716,BMG_DS023921,,Hypofunction and other disorders of the pituitary gland,,,,E23,,,C0494308,,,,,
+BMGC_DS06717,BMG_DS023923,,Other disorders of adrenal gland,,,,E27,,,C0494313,,,,,
+BMGC_DS06718,BMG_DS023929,,Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism,,,,E71,,,C0494332,,,,,
+BMGC_DS06719,BMG_DS023930,,Other disorders of amino-acid metabolism,,,,E72,,,C0494334,,,,,
+BMGC_DS06720,BMG_DS023931,,Other disorders of carbohydrate metabolism,,,,E74,,,C0494336,,,,,
+BMGC_DS06721,BMG_DS023932,,Disorders of sphingolipid metabolism and other lipid storage disorders,,,,E75,,,C0494338,,,,,
+BMGC_DS06722,BMG_DS023934,,Disorders of porphyrin and bilirubin metabolism,,,,E80,,,C0494347,,,,,
+BMGC_DS06723,BMG_DS023939,,"Lipodystrophy, not elsewhere classified",,5D2Z,"Metabolic disorders, unspecified",E88.1,DOID:0111137;DOID:0111136;DOID:0111138;DOID:0111135,congenital generalized lipodystrophy type 2 | congenital generalized lipodystrophy type 4 | congenital generalized lipodystrophy type 1 | congenital generalized lipodystrophy type 3,C0494360,,,,,
+BMGC_DS06724,BMG_DS023950,,Spinal muscular atrophy and related syndromes,,,,G12,,,C0494452,,,,,
+BMGC_DS06725,BMG_DS023954,,"Alzheimer Disease, Late Onset",Alzheimer Disease,,,,,,C0494463,D000544,,,,
+BMGC_DS06726,BMG_DS023955,,"Other degenerative diseases of nervous system, not elsewhere classified",,,,G31,,,C0494464,,,,,
+BMGC_DS06727,BMG_DS023965,,Mononeuropathies,Mononeuropathies,,,,DOID:1188,mononeuropathy,C0494491,D020422,,MONDO:0001397,mononeuropathy,
+BMGC_DS06728,BMG_DS023971,,Other disorders of brain,,,,G93,,,C0494513,,,,,
+BMGC_DS06729,BMG_DS023987,,,,,,,DOID:2952,inner ear disease,C0494559,,,MONDO:0002467,inner ear disorder,
+BMGC_DS06730,BMG_DS023988,,"Other disorders of ear, not elsewhere classified",,,,H93,,,C0494566,,,,,
+BMGC_DS06731,BMG_DS023995,,Other pulmonary heart diseases,,,,I27,,,C0494585,,,,,
+BMGC_DS06732,BMG_DS024047,,"Noninfective gastroenteritis and colitis, unspecified",,DE2Z,"Diseases of the digestive system, unspecified",K52.9,DOID:0060190,ileocolitis,C0494762,,,,,
+BMGC_DS06733,BMG_DS024076,,Other nonscarring hair loss,,,,L65,,,C0494856,,,,,
+BMGC_DS06734,BMG_DS024078,,Other follicular disorders,,,,L73,,,C0494864,,,,,
+BMGC_DS06735,BMG_DS024085,,Other rheumatoid arthritis,,,,M06,,,C0494897,,,,,
+BMGC_DS06736,BMG_DS024086,,Other arthritis,,,,M13,,,C0494904,,,,,
+BMGC_DS06737,BMG_DS024090,,"Other joint disorder, not elsewhere classified",,,,M25,,,C0494938,,,,,
+BMGC_DS06738,BMG_DS024108,,Other disorders of bone density and structure,,,,M85,,,C0495004,,,,,
+BMGC_DS06739,BMG_DS024109,,Other disorders of bone,,,,M89,,,C0495006,,,,,
+BMGC_DS06740,BMG_DS024140,,,,,,,DOID:12735,hernia of ovary and fallopian tube,C0495094,,,,,
+BMGC_DS06741,BMG_DS024172,,Noninfective neonatal diarrhea,,KB8C,Noninfectious neonatal diarrhoea,P78.3,DOID:0060779;DOID:0060776;DOID:0060777;DOID:0060780;DOID:0060781;DOID:0060778,congenital secretory sodium diarrhea 3 | congenital diarrhea 6 | congenital secretory sodium diarrhea 8 | congenital diarrhea 5 with tufting enteropathy | congenital diarrhea 7 with exudative enteropathy | congenital malabsorptive diarrhea 4,C0495452,,,,,
+BMGC_DS06742,BMG_DS024179,,,,,,,DOID:8712,neurofibromatosis,C0495632,,,,,
+BMGC_DS06743,BMG_DS024180,,Other specified congenital malformation syndromes affecting multiple systems,,,,Q87,,,C0495636,,,,,
+BMGC_DS06744,BMG_DS024181,,Congenital malformation syndromes involving early overgrowth,,LD2C,Overgrowth syndromes,Q87.3,DOID:0080351,CLOVES syndrome,C0495640,,,,,
+BMGC_DS06745,BMG_DS024184,,,,,,,DOID:8649,tongue cancer,C0496755,,,,,
+BMGC_DS06746,BMG_DS024185,,,,,,,DOID:8618,oral cavity cancer,C0496758,,,,,
+BMGC_DS06747,BMG_DS024187,,,,,,,DOID:8133,epiglottis cancer,C0496765,,,,,
+BMGC_DS06748,BMG_DS024188,,,,,,,DOID:8660,postcricoid region cancer,C0496769,,,MONDO:0004635,postcricoid region cancer,
+BMGC_DS06749,BMG_DS024189,,,,,,,DOID:8533,hypopharynx cancer,C0496770,,,,,
+BMGC_DS06750,BMG_DS024191,,,,,,,DOID:5041,esophageal cancer,C0496775,,,MONDO:0021324,malignant neoplasm of abdominal esophagus,
+BMGC_DS06751,BMG_DS024192,,,,,,,DOID:11239,appendix cancer,C0496779,,,MONDO:0001235,appendix cancer,
+BMGC_DS06752,BMG_DS024193,,,,,,,DOID:1799,islet cell tumor,C0496784,,,,,
+BMGC_DS06753,BMG_DS024195,,,,,,,DOID:11905,labium majus cancer,C0496814,,,MONDO:0001403,labium majus cancer,
+BMGC_DS06754,BMG_DS024196,,,,,,,DOID:1243,labia minora cancer,C0496815,,,MONDO:0001526,labia minora cancer,
+BMGC_DS06755,BMG_DS024197,,,,,,,DOID:11813,bladder trigone cancer,C0496826,,,MONDO:0001375,bladder trigone cancer,
+BMGC_DS06756,BMG_DS024198,,,,,,,DOID:11820,bladder dome cancer,C0496827,,,MONDO:0001380,bladder dome cancer,
+BMGC_DS06757,BMG_DS024199,,,,,,,DOID:11593,bladder lateral wall cancer,C0496828,,,MONDO:0001319,bladder lateral wall cancer,
+BMGC_DS06758,BMG_DS024200,,,,,,,DOID:4352,ciliary body cancer,C0496833,,,MONDO:0002969,ciliary body cancer,
+BMGC_DS06759,BMG_DS024202,,,,,,,DOID:370,malignant olfactory nerve neoplasm,C0496838,,,MONDO:0851100,malignant olfactory nerve neoplasm,
+BMGC_DS06760,BMG_DS024203,,,,,,,DOID:1785,pituitary cancer,C0496842,,,MONDO:0002109,pituitary cancer,
+BMGC_DS06761,BMG_DS024204,,,,,,,DOID:9132,liver carcinoma in situ,C0496854,,,,,
+BMGC_DS06762,BMG_DS024216,139134006;30746006;271821001;161878009,Lymphadenopathy,Lymphadenopathy,,,,,,C0497156,D000072281,MTHU002630,,,Lymphadenopathy | Lymphadenopathy (finding) | Enlargement of lymph nodes | Lymphadenopathy | Swelling of lymph nodes | Lymphadenopathy (disorder)
+BMGC_DS06763,BMG_DS024218,,,,,,,DOID:176,cardiovascular cancer,C0497243,,,MONDO:0024757,cardiovascular neoplasm,
+BMGC_DS06764,BMG_DS024220,,,,,,,,,C0497327,,,MONDO:0001627,dementia,
+BMGC_DS06765,BMG_DS024224,,,,,,,,,C0497552,,,MONDO:0002320,congenital nervous system disorder,
+BMGC_DS06766,BMG_DS024229,64479007,Pneumonia due to Klebsiella pneumoniae,,CA40.03,Pneumonia due to Klebsiella pneumoniae,J15.0,,,C0519030,,,MONDO:0030602,Klebsiella pneumonia,Pneumonia caused by Klebsiella pneumoniae (disorder) | Pneumonia caused by Klebsiella pneumoniae
+BMGC_DS06767,BMG_DS024231,,,,,,,DOID:1523,colon lymphoma,C0519037,,,MONDO:0002035,colon lymphoma,
+BMGC_DS06768,BMG_DS024234,,,,,,,DOID:6760,lung lymphoma,C0519063,,,,,
+BMGC_DS06769,BMG_DS024238,,Necrotizing Enterocolitis,"Enterocolitis, Necrotizing",,,,DOID:8677,perinatal necrotizing enterocolitis,C0520459,D020345,,MONDO:0005313,necrotizing enterocolitis,
+BMGC_DS06770,BMG_DS024241,,,,,,,DOID:13918;DOID:4737,somatization disorder | somatoform disorder,C0520482,,,MONDO:0001830,somatization disorder,
+BMGC_DS06771,BMG_DS024261,48124008,Fibrosis of bile duct,,,,,,,C0520571,,,MONDO:0041959,fibrosis of bile duct,Fibrosis of bile duct | Biliary duct fibrosis | Biliary sclerosis | Fibrosis of bile duct (disorder)
+BMGC_DS06772,BMG_DS024264,36689008;266620001;155862004;22352007,Acute pyelonephritis,,,,N10,DOID:559,acute pyelonephritis,C0520575,,,MONDO:0003529,acute pyelonephritis,Acute pyelonephritis | Acute pyelonephritis (disorder) | Acute PN - pyelonephritis | APN - Acute pyelonephritis | Acute kidney infection | (Acute pyelonephritis) or (acute pyonephrosis) | Acute pyonephrosis | Acute pyelonephritis | Pyonephrosis - acute | (Acute pyelonephritis) or (acute pyonephrosis) (disorder) | Acute pyonephrosis | Acute pyelonephritis | Pyonephrosis - acute | (Acute pyelonephritis) or (acute pyonephrosis) | (Acute pyelonephritis) or (acute pyonephrosis) (disorder) | Acute bacterial tubulointerstitial nephritis | Acute bacterial tubulointerstitial nephritis (disorder) | Acute bacterial TIN (tubulointerstitial nephritis)
+BMGC_DS06773,BMG_DS024266,52620003,Urethral atrophy,,,,,,,C0520577,,,,,Urethral atrophy | Urethral atrophy (disorder)
+BMGC_DS06774,BMG_DS024274,,"Sleep Apnea, Obstructive","Sleep Apnea, Obstructive",,,,DOID:0050848,obstructive sleep apnea,C0520679,D020181,107650,MONDO:0007147,obstructive sleep apnea syndrome,
+BMGC_DS06775,BMG_DS024275,,"Sleep Apnea, Central","Sleep Apnea, Central",,,,DOID:9220,central sleep apnea,C0520680,D020182,,,,
+BMGC_DS06776,BMG_DS024283,,Opticocochleodentate Degeneration,,,,,,,C0520711,C563002,258700,MONDO:0009790,Opticocochleodentate degeneration,
+BMGC_DS06777,BMG_DS024286,42369001,Pallidopontonigral degeneration,,,,,DOID:9255,frontotemporal dementia,C0520716,,,,,Pallidopontonigral degeneration | Pallidopontonigral degeneration (disorder)
+BMGC_DS06778,BMG_DS024288,,Spinopontine Atrophy,"Muscular Disorders, Atrophic",,,,,,C0520719,D020966,,,,
+BMGC_DS06779,BMG_DS024293,,Retraction Nystagmus,"Nystagmus, Pathologic",,,,,,C0520731,D009759,,,,
+BMGC_DS06780,BMG_DS024298,9434008;58864003,Hereditary pyropoikilocytosis,,,,,,,C0520739,,266140,MONDO:0009948,"pyropoikilocytosis, hereditary",Hereditary pyropoikilocytosis | Hereditary pyropoikilocytosis (disorder) | HPP - hereditary pyropoikilocytosis | Hereditary elliptocytosis | Hereditary elliptocytosis (disorder)
+BMGC_DS06781,BMG_DS024307,73028002,Staphylococcal endocarditis,,,,,,,C0520767,,,,,Staphylococcal endocarditis | Staphylococcal endocarditis (disorder)
+BMGC_DS06782,BMG_DS024313,60867007,Klebsiella cystitis,,,,,,,C0520775,,,,,Klebsiella cystitis | Klebsiella cystitis (disorder)
+BMGC_DS06783,BMG_DS024314,188463006;73107008,Chlamydial pelvic inflammatory disease,,,,,,,C0520777,,,,,Chlamydial pelvic inflammatory disease | Chlamydial pelvic inflammatory disease (disorder) | Pelvic inflammation with female sterility due to Chlamydia trachomatis | Pelvic inflammation with female sterility due to Chlamydia trachomatis (disorder)
+BMGC_DS06784,BMG_DS024361,,Brain Stem Infarctions,Brain Stem Infarctions,,,,DOID:3523,brain stem infarction,C0521542,D020526,,MONDO:0006686,brain stem infarction,
+BMGC_DS06785,BMG_DS024365,,,,,,,,,C0521573,,,MONDO:0020357,coloboma of eyelid,
+BMGC_DS06786,BMG_DS024377,,Peritoneal Fibrosis,Peritoneal Fibrosis,,,,,,C0521607,D056627,,,,
+BMGC_DS06787,BMG_DS024379,,Emphysematous Cholecystitis,Emphysematous Cholecystitis,,,,DOID:9765,emphysematous cholecystitis,C0521610,D041882,,MONDO:0005742,emphysematous cholecystitis,
+BMGC_DS06788,BMG_DS024393,95619009,Neonatal respiratory failure,,,,,DOID:11161,neonatal respiratory failure,C0521648,,MTHU043071,MONDO:0001207,neonatal respiratory failure,Neonatal respiratory failure | Neonatal respiratory failure (disorder)
+BMGC_DS06789,BMG_DS024397,,"Motor Neuron Disease, Upper",Motor Neuron Disease,,,,,,C0521659,D016472,,,,
+BMGC_DS06790,BMG_DS024398,,Acute Confusional Migraine,Migraine Disorders,,,,,,C0521664,D008881,,,,
+BMGC_DS06791,BMG_DS024401,,Primary Thunderclap Headache,"Headache Disorders, Primary",,,,,,C0521668,D051270,,,,
+BMGC_DS06792,BMG_DS024422,405722004,Atrophic retina,,,,,,,C0521694,,,,,Atrophic retina (disorder) | Atrophic retina | Retinal atrophy
+BMGC_DS06793,BMG_DS024429,193618003;95722004,Bilateral cataracts (disorder),,,,,,,C0521707,,,,,Bilateral cataracts | Bilateral cataracts (disorder) | Bilateral cataracts | Bilateral cataracts (disorder) | Cataracts
+BMGC_DS06794,BMG_DS024440,,"Corneal dystrophy, epithelial basement membrane",,,,,DOID:0060447,epithelial basement membrane dystrophy,C0521723,C535477,121820,MONDO:0007375,epithelial basement membrane dystrophy,
+BMGC_DS06795,BMG_DS024448,95758006,Lower eyelid ectropion,,,,,,,C0521736,,,,,Lower eyelid ectropion | Lower eyelid turned out | Ectropion of lower lid | Lower eyelid ectropion (disorder)
+BMGC_DS06796,BMG_DS024460,,Temporary Nystagmus,"Nystagmus, Pathologic",,,,,,C0521753,D009759,,,,
+BMGC_DS06797,BMG_DS024461,,Permanent Nystagmus,"Nystagmus, Pathologic",,,,,,C0521754,D009759,,,,
+BMGC_DS06798,BMG_DS024462,,Unidirectional Nystagmus,"Nystagmus, Pathologic",,,,,,C0521755,D009759,,,,
+BMGC_DS06799,BMG_DS024463,,Multidirectional Nystagmus,"Nystagmus, Pathologic",,,,,,C0521756,D009759,,,,
+BMGC_DS06800,BMG_DS024464,,Conjugate Nystagmus,"Nystagmus, Pathologic",,,,,,C0521757,D009759,,,,
+BMGC_DS06801,BMG_DS024465,,Convergence Nystagmus,"Nystagmus, Pathologic",,,,,,C0521759,D009759,,,,
+BMGC_DS06802,BMG_DS024466,,Fatigable Positional Nystagmus,"Nystagmus, Pathologic",,,,,,C0521760,D009759,,,,
+BMGC_DS06803,BMG_DS024467,,Non-Fatigable Positional Nystagmus,"Nystagmus, Pathologic",,,,,,C0521761,D009759,,,,
+BMGC_DS06804,BMG_DS024482,111571009,Congenital atransferrinemia,,,,,,,C0521802,C538259,209300,MONDO:0008846,atransferrinemia,Congenital atransferrinemia | Congenital atransferrinaemia | Congenital atransferrinemia (disorder)
+BMGC_DS06805,BMG_DS024514,,Primary Exertional Headache,"Headache Disorders, Primary",,,,,,C0522253,D051270,,,,
+BMGC_DS06806,BMG_DS024522,,,,,,,,,C0522624,,618398,MONDO:0019475,subcutaneous panniculitis-like T-cell lymphoma,
+BMGC_DS06807,BMG_DS024523,,,,,,,DOID:0081084,acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22),C0522630,,,,,
+BMGC_DS06808,BMG_DS024524,,,,,,,DOID:0081085,acute myeloid leukemia with minimal differentiation,C0522631,,,MONDO:0005223,acute myeloid leukemia with minimal differentiation,
+BMGC_DS06809,BMG_DS024526,,Pseudoaphakia,Cataract,,,,,,C0524524,D002386,116100,MONDO:0007284,cataract 20 multiple types,
+BMGC_DS06810,BMG_DS024527,,,,,,,,,C0524528,,,MONDO:0000594,pervasive developmental disorder,
+BMGC_DS06811,BMG_DS024529,,Mulibrey Nanism,Mulibrey Nanism,,,,DOID:0050436,mulibrey nanism,C0524582,D050336,253250,MONDO:0009664,mulibrey nanism,
+BMGC_DS06812,BMG_DS024530,,Chronic Alcoholic Hepatitis,"Hepatitis, Alcoholic",,,,,,C0524610,D006519,,,,
+BMGC_DS06813,BMG_DS024531,,Cryptogenic Chronic Hepatitis,"Hepatitis, Chronic",,,,,,C0524611,D006521,,,,
+BMGC_DS06814,BMG_DS024532,,Metabolic Syndrome X,Metabolic Syndrome,,,,DOID:14221,abdominal obesity-metabolic syndrome 1,C0524620,D024821,,,,
+BMGC_DS06815,BMG_DS024533,,Lymphatism,Lymphatic Diseases,,,,,,C0524631,D008206,,,,
+BMGC_DS06816,BMG_DS024534,,Status Lymphaticus,Lymphatic Diseases,,,,,,C0524632,D008206,,,,
+BMGC_DS06817,BMG_DS024535,,,,,,,DOID:2559,opiate dependence,C0524662,,,MONDO:0005530,opiate dependence,
+BMGC_DS06818,BMG_DS024536,,Neuropapillitis,Optic Neuritis,,,,,,C0524679,D009902,,,,
+BMGC_DS06819,BMG_DS024537,,"Periodontitis, Acute Nonsuppurative",Periapical Periodontitis,,,,,,C0524686,D010485,,,,
+BMGC_DS06820,BMG_DS024538,,Meningeal Plague,Plague,,,,,,C0524687,D010930,,,,
+BMGC_DS06821,BMG_DS024539,,Pneumonic Plague,Plague,,,,DOID:10398,pneumonic plague,C0524688,D010930,,MONDO:0001024,pneumonic plague,
+BMGC_DS06822,BMG_DS024540,,Pulmonary Thromboembolisms,Pulmonary Embolism,,,,,,C0524702,D011655,,,,
+BMGC_DS06823,BMG_DS024545,,"Lung, Hyperlucent","Lung, Hyperlucent",,,,DOID:10032,hyperlucent lung,C0524799,D019568,,MONDO:0000925,hyperlucent lung,
+BMGC_DS06824,BMG_DS024546,,,,,,,DOID:4645,retinal cancer,C0524801,,,MONDO:0021231,retina neoplasm,
+BMGC_DS06825,BMG_DS024547,,,,,,,DOID:3419,optic nerve neoplasm,C0524802,,,MONDO:0002640,optic nerve neoplasm,
+BMGC_DS06826,BMG_DS024548,,Intracranial Hypotension,Intracranial Hypotension,,,,DOID:4723,intracranial hypotension,C0524812,D019585,,MONDO:0006811,intracranial hypotension,
+BMGC_DS06827,BMG_DS024549,,Neurodegenerative Disorders,Neurodegenerative Diseases,,,,DOID:1289,neurodegenerative disease,C0524851,D019636,,,,
+BMGC_DS06828,BMG_DS024550,,"Hepatitis B, Chronic","Hepatitis B, Chronic",,,,,,C0524909,D019694,,MONDO:0005366,chronic hepatitis B virus infection,
+BMGC_DS06829,BMG_DS024551,,"Hepatitis C, Chronic","Hepatitis C, Chronic",,,,,,C0524910,D019698,,MONDO:0005354,chronic hepatitis C virus infection,
+BMGC_DS06830,BMG_DS024553,,"Hepatitis, Chronic, Drug-Induced","Chemical and Drug Induced Liver Injury, Chronic",,,,DOID:2044,drug-induced hepatitis,C0524912,D056487,,,,
+BMGC_DS06831,BMG_DS024554,,Schnitzler Syndrome,Schnitzler Syndrome,,,,DOID:4371,Schnitzler syndrome,C0524988,D019873,,MONDO:0018304,Schnitzler syndrome,
+BMGC_DS06832,BMG_DS024555,,,,,,,DOID:3324,mood disorder,C0525045,,,MONDO:0005371,mood disorder,
+BMGC_DS06833,BMG_DS024558,191371001;36874002,Stress polycythemia,,,,,DOID:2838,stress polycythemia,C0541719,,,,,Spurious polycythaemia | Stress polycythaemia | Stress polycythemia | Spurious polycythemia | Stress polycythemia (disorder) | Stress polycythemia | Emotional polycythemia | Stress polycythaemia | Emotional polycythaemia | Stress polycythemia (disorder)
+BMGC_DS06834,BMG_DS024559,,,,,,,,,C0541782,,,MONDO:0015281,atrial standstill,
+BMGC_DS06835,BMG_DS024560,,,,,,,,,C0541794,,,MONDO:0004323,muscular atrophy,
+BMGC_DS06836,BMG_DS024561,,,,,,,DOID:10021,duodenum cancer,C0541912,,,MONDO:0021335,carcinoma of duodenum,
+BMGC_DS06837,BMG_DS024565,314207007,Non-Q wave myocardial infarction,,,,,,,C0542269,,,,,Non-Q wave myocardial infarction | Non-Q wave myocardial infarction (disorder)
+BMGC_DS06838,BMG_DS024573,,,,,,,,,C0542428,,,MONDO:0019669,hypochondrogenesis,
+BMGC_DS06839,BMG_DS024575,,,,,,,,,C0542519,,,MONDO:0018470,renal agenesis,
+BMGC_DS06840,BMG_DS024576,,,,,,,DOID:6112,cerebral meningioma,C0542564,,,MONDO:0003772,cerebral meningioma,
+BMGC_DS06841,BMG_DS024577,,Glycogen Storage Disease IXB,,,,,DOID:0111041,glycogen storage disease IXb,C0543514,C563008,261750,MONDO:0009868,glycogen storage disease IXb,
+BMGC_DS06842,BMG_DS024579,,Glycinuria with or without Oxalate Urolithiasis,,,,,,,C0543541,C563009,138500,MONDO:0007677,hyperglycinuria,
+BMGC_DS06843,BMG_DS024591,,Idiopathic Autoimmune Hemolytic Anemia,"Anemia, Hemolytic, Autoimmune",,,,,,C0543663,D000744,,,,
+BMGC_DS06844,BMG_DS024596,,"Neutrophilia, Hereditary",,,,,DOID:0090120,hereditary neutrophilia,C0543669,C563010,162830,MONDO:0008092,hereditary neutrophilia,
+BMGC_DS06845,BMG_DS024600,,"Klinefelter Syndrome, Variants",Klinefelter Syndrome,,,,,,C0543754,D007713,,,,
+BMGC_DS06846,BMG_DS024602,,Idiopathic hypercalciuria,,,,R82.994,,,C0543800,,,,,
+BMGC_DS06847,BMG_DS024607,129573006,Atherosclerotic occlusive disease,,,,,,,C0543822,,,,,Atherosclerotic ischaemic disease | Atherosclerotic ischemic disease | Atherosclerotic occlusive disease | Atherosclerotic occlusive disease (disorder)
+BMGC_DS06848,BMG_DS024609,,"Motor Neuron Disease, Secondary",Motor Neuron Disease,,,,,,C0543858,D016472,,,,
+BMGC_DS06849,BMG_DS024610,,"Amyotrophic Lateral Sclerosis, Guam Form",Amyotrophic Lateral Sclerosis,,,,DOID:0111246,amyotrophic lateral sclerosis-parkinsonism/dementia complex 1,C0543859,D000690,105500,MONDO:0007104,amyotrophic lateral sclerosis-parkinsonism-dementia complex,
+BMGC_DS06850,BMG_DS024611,,"Apraxia, oculomotor, Cogan type",,,,,,,C0543874,C537423,257550,MONDO:0009764,"ocular motor apraxia, Cogan type",
+BMGC_DS06851,BMG_DS024613,723125008,Epileptic encephalopathy,,,,,,,C0543888,,MTHU028611,,,Epileptic encephalopathy (disorder) | Epileptic encephalopathy | EE - epileptic encephalopathy
+BMGC_DS06852,BMG_DS024614,,,,,,,,,C0543918,,605419,MONDO:0011552,schizophrenia 10,
+BMGC_DS06853,BMG_DS024615,392481002;404632009,Chandler syndrome,,,,,DOID:11554,Chandler syndrome,C0544008,,,MONDO:0020369,Chandler syndrome,Chandler syndrome (disorder) | Chandler syndrome | Chandler's syndrome (disorder) | Chandler's syndrome | Chandler syndrome
+BMGC_DS06854,BMG_DS024618,,Elephantiasis Nostras Verrucosa,Elephantiasis,,,,DOID:0050138,podoconiosis,C0544766,D004604,,,,
+BMGC_DS06855,BMG_DS024621,,"Myositis, Proliferative",Myositis,,,,,,C0544796,D009220,,,,
+BMGC_DS06856,BMG_DS024629,,,,,,,,,C0544855,,151600,MONDO:0007900,nonsyndromic congenital nail disorder 3,
+BMGC_DS06857,BMG_DS024630,,,,,,,,,C0544862,,249400,MONDO:0009578,neurocutaneous melanocytosis,
+BMGC_DS06858,BMG_DS024633,,Acrokeratoelastoidosis of Costa,,,,,DOID:0060362,punctate palmoplantar keratoderma type III,C0545044,C535653,101850,MONDO:0007047,punctate palmoplantar keratoderma type III,
+BMGC_DS06859,BMG_DS024634,,,,,,,DOID:5709,mixed-type liposarcoma,C0545074,,,MONDO:0020561,myxoid/round cell liposarcoma,
+BMGC_DS06860,BMG_DS024635,,,,,,,DOID:5820,composite lymphoma,C0545080,,,MONDO:0005710,composite lymphoma,
+BMGC_DS06861,BMG_DS024638,,"Nemaline Myopathy, Childhood Onset","Myopathies, Nemaline",,,,,,C0546125,D017696,,MONDO:0015738,childhood-onset nemaline myopathy,
+BMGC_DS06862,BMG_DS024640,,Congenital Fiber Type Disproportion,"Myopathies, Structural, Congenital",,,,,,C0546264,D020914,,MONDO:0009711,congenital fiber-type disproportion myopathy,
+BMGC_DS06863,BMG_DS024643,1162266005,Exudative glomerulonephritis,,,,,DOID:4777,exudative glomerulonephritis,C0546345,,,MONDO:0003133,exudative glomerulonephritis,Exudative glomerulonephritis (disorder) | Exudative glomerulonephritis
+BMGC_DS06864,BMG_DS024651,,,,,,,,,C0546476,,132800,MONDO:0007566,multiple self-healing squamous epithelioma,
+BMGC_DS06865,BMG_DS024653,186994008;266151007,Dermatophytosis of the body,,,,,DOID:12179,tinea corporis,C0546826,,,,,Dermatophytosis of the body | Herpes circinatus | Tinea corporis | (Dermatophytosis of the body) or (herpes circinatus) or (tinea corporis) | (Dermatophytosis of the body) or (herpes circinatus) or (tinea corporis) (disorder) | Dermatophytosis of the body | Dermatophytosis of the body (disorder)
+BMGC_DS06866,BMG_DS024654,,,,,,,DOID:12298,intrahepatic gall duct cancer,C0546835,,,MONDO:0001487,intrahepatic bile duct cancer,
+BMGC_DS06867,BMG_DS024655,,,,,,,,,C0546837,,133239,MONDO:0007576,esophageal cancer,
+BMGC_DS06868,BMG_DS024656,18191000,Nodding spasm,,,,,,,C0546878,,,MONDO:0017201,Spasmus nutans,Nodding spasm | Salaam spasm | Salaam spasm (finding)
+BMGC_DS06869,BMG_DS024664,,,,,,,DOID:0050472,monilethrix,C0546966,,158000;252200,MONDO:0008009,monilethrix,
+BMGC_DS06870,BMG_DS024665,,,,,,,,,C0546969,,128700,MONDO:0007501,"preauricular fistulae, congenital",
+BMGC_DS06871,BMG_DS024673,187115002;86711009,Cutaneous schistosomiasis,,,,,DOID:11302,cercarial dermatitis,C0546996,,,MONDO:0001260,cercarial dermatitis,Cutaneous schistosomiasis | Schistosome dermatitis | Clam-digger's itch | Schistosomal cercarial dermatitis | Infection by cercariae of schistosoma | Swamp itch | Swimmers' itch | Swimmer's itch | Cercarial dermatitis | Clam digger's itch | Cutaneous schistosomiasis (disorder) | Infection by cercariae of schistosoma | Infection by cercariae of schistosoma (disorder)
+BMGC_DS06872,BMG_DS024674,,"Larva Migrans, Cutaneous",Larva Migrans,,,,,,C0546999,D007815,,MONDO:0018500,cutaneous larva migrans,
+BMGC_DS06873,BMG_DS024676,,,,,,,,,C0547065,,,MONDO:0016702,oligoastrocytoma,
+BMGC_DS06874,BMG_DS024687,399205006;201187009;238494006,Pseudofolliculitis barbae (disorder),,,,,,,C0549150,,612318,MONDO:0012865,Pseudofolliculitis barbae,Pseudofolliculitis barbae (disorder) | Pseudofolliculitis barbae | Pseudofolliculitis barbae | Pseudofolliculitis barbae (disorder)
+BMGC_DS06875,BMG_DS024689,,North Asian Tick Typhus,Spotted Fever Group Rickettsiosis,,,,DOID:10921,Siberian tick typhus,C0549160,D000073605,,MONDO:0001154,Siberian tick typhus,
+BMGC_DS06876,BMG_DS024698,193914004;309779001,Meibomianitis,Meibomitis,,,,,,C0549398,D000092663,,,,Meibomianitis | Meibomianitis (disorder) | Meibomianitis | Meibomianitis (disorder) | Meibomitis
+BMGC_DS06877,BMG_DS024700,,Obstructive Hydrocephalus,Hydrocephalus,,,,DOID:14159,obstructive hydrocephalus,C0549423,D006849,,MONDO:0001896,obstructive hydrocephalus,
+BMGC_DS06878,BMG_DS024701,,,,,,,,,C0549463,,,MONDO:0010627,X-linked lymphoproliferative syndrome,
+BMGC_DS06879,BMG_DS024703,359633007;47891005,Preglaucoma,,,,,DOID:9283,borderline glaucoma,C0549470,,,,,Preglaucoma | Preglaucoma (disorder) | Borderline glaucoma | Borderline glaucoma (disorder)
+BMGC_DS06880,BMG_DS024704,,,,,,,DOID:8007,Pancoast tumor,C0549471,,,MONDO:0006883,malignant superior sulcus neoplasm,
+BMGC_DS06881,BMG_DS024706,,,,,,,DOID:3963,thyroid gland carcinoma,C0549473,,,MONDO:0015075,thyroid gland carcinoma,
+BMGC_DS06882,BMG_DS024707,,Pigmentation Disorders,Pigmentation Disorders,,,,,,C0549567,D010859,,MONDO:0006562,obsolete incontinentia pigmenti achromians,
+BMGC_DS06883,BMG_DS024709,,,,,,,DOID:1876,sexual dysfunction,C0549622,,,,,
+BMGC_DS06884,BMG_DS024712,,Necrotizing Arteritis,Polyarteritis Nodosa,,,,,,C0553548,D010488,,,,
+BMGC_DS06885,BMG_DS024713,,Jackknife Seizures,"Spasms, Infantile",,,,DOID:0050562,West syndrome,C0553558,D013036,,,,
+BMGC_DS06886,BMG_DS024719,,,,,,,DOID:3369,Ewing sarcoma,C0553580,,612219,MONDO:0012817,Ewing sarcoma,
+BMGC_DS06887,BMG_DS024720,403820003,Cafe-au-lait macules with pulmonary stenosis,,,,,,,C0553586,,193520,MONDO:0008672,Watson syndrome,Café-au-lait macules with pulmonary stenosis (disorder) | Café-au-lait macules with pulmonary stenosis | Watson syndrome | Cafe-au-lait macules with pulmonary stenosis
+BMGC_DS06888,BMG_DS024722,,Myotonic Disorders,Myotonic Disorders,,,,DOID:0050759;DOID:450,myotonic dystrophy type 2 | myotonic disease,C0553604,D020967,,MONDO:0016120,myotonic syndrome,
+BMGC_DS06889,BMG_DS024726,15033003;102453009,Peritonsillar cellulitis,,,,,,,C0553656,,,,,Peritonsillar abscess | Quinsy | Angina tonsillaris | Peritonsillar abscess (disorder) | Peritonsillar cellulitis | Peritonsillar cellulitis (disorder) | Acute peritonsillitis
+BMGC_DS06890,BMG_DS024729,234457009,Hypofibrinogenemia,,,,,,,C0553681,,MTHU009690,,,Hypofibrinogenaemia | Hypofibrinogenemia | Hypofibrinogenemia (disorder)
+BMGC_DS06891,BMG_DS024732,,,,,,,DOID:305,carcinoma,C0553707,,,,,
+BMGC_DS06892,BMG_DS024734,,,,,,,DOID:3151,skin squamous cell carcinoma,C0553723,,,MONDO:0002529,skin squamous cell carcinoma,
+BMGC_DS06893,BMG_DS024735,60782007;239832006,Calcium pyrophosphate deposition disease,,,,,,,C0553730,,,MONDO:0001314,chondrocalcinosis,Pseudogout | Idiopathic articular chondrocalcinosis | Chondrocalcinosis due to pyrophosphate crystals | Chondrocalcinosis articularis | Pseudogout (disorder) | CPPD - Calcium pyrophosphate deposition disease | CPDD - Calcium pyrophosphate deposition disease | Calcium pyrophosphate deposition disease | Calcium pyrophosphate deposition disease (disorder)
+BMGC_DS06894,BMG_DS024743,,Olfaction Disorders,Olfaction Disorders,,,,,,C0553757,D000857,,,,
+BMGC_DS06895,BMG_DS024750,,Congenital Cerebral Palsy,Cerebral Palsy,,,,,,C0553767,D002547,,,,
+BMGC_DS06896,BMG_DS024772,,,,,,,DOID:12932,endomyocardial fibrosis,C0553980,,,MONDO:0006746,endomyocardial fibrosis,
+BMGC_DS06897,BMG_DS024821,,"Polymyositis, Idiopathic",Polymyositis,,,,DOID:0080745,polymyositis,C0554591,D017285,,,,
+BMGC_DS06898,BMG_DS024827,268005002,Synovial plica (disorder),,,,,,,C0554601,,,MONDO:0001468,synovial plica syndrome,Synovial plica | Synovial plica (disorder)
+BMGC_DS06899,BMG_DS024834,,Group A Streptococcal Infections,Streptococcal Infections,,,,,,C0554628,D013290,,,,
+BMGC_DS06900,BMG_DS024837,302812006,Anogenital human papillomavirus infection,,,,,DOID:11168,anogenital venereal wart,C0554632,,,MONDO:0005647,anogenital human papillomavirus infection,Anogenital human papilloma virus infection | HPV - Anogenital human papilloma virus infection | WVI - Genital wart virus infection | Genital wart virus infection | Anogenital human papillomavirus infection | Anogenital human papillomavirus infection (disorder)
+BMGC_DS06901,BMG_DS024846,,,,,,,DOID:4292,morpheaform basal cell carcinoma,C0555191,,,MONDO:0002949,morpheaform basal cell carcinoma,
+BMGC_DS06902,BMG_DS024848,,,,,,,DOID:3070,high grade glioma,C0555198,,,MONDO:0100342,malignant glioma,
+BMGC_DS06903,BMG_DS024850,,,,,,,,,C0555206,,207950,MONDO:0008816,Chiari malformation type II,
+BMGC_DS06904,BMG_DS024851,,,,,,,,,C0555214,,219600,MONDO:0009060,cystic disease of lung,
+BMGC_DS06905,BMG_DS024859,275393007,Oral infection,,,,,,,C0555971,,,,,Infection mouth | Oral infection | Oral infection (disorder)
+BMGC_DS06906,BMG_DS024884,266173000;154268000;274080003,Bacterial gastroenteritis,,,,,,,C0558348,,,,,Specific GIT infectious dis. | Specific gastrointestinal infectious disease | Dysentery | Bacterial gastroenteritis | Gastroenteritis - bact. | Diarrhoea-bact.GIT inf. | (Specific GIT infectious disease) or (dysentery) or (bacterial: [gastroenteritis] or [diarrhoea]) | Diarrhea-bact.GIT inf. | (Specific GIT infectious disease) or (dysentery) or (bacterial: [gastroenteritis] or [diarrhea]) | (Specific GIT infectious disease) or (dysentery) or (bacterial: [gastroenteritis] or [diarrhoea]) (disorder) | (Specific GIT infectious disease) or (dysentery) or (bacterial: [gastroenteritis] or [diarrhea]) | Gastroenteritis - bact. | Specific GIT infectious dis. | Specific gastrointestinal infectious disease | Dysentery | Bacterial gastroenteritis | (Specific GIT infectious disease) or (dysentery) or (bacterial: [gastroenteritis] or [diarrhoea]) | Diarrhea-bact.GIT inf. | Diarrhoea-bact.GIT inf. | (Specific GIT infectious disease) or (dysentery) or (bacterial: [gastroenteritis] or [diarrhoea]) (disorder) | Bacterial gastroenteritis | Bacterial gastroenteritis (disorder)
+BMGC_DS06907,BMG_DS024901,145274002;270032007;274401005,Uric acid renal calculus,,,,,,,C0558595,,,,,Uric acid renal calculus &/or O/E | Uric acid renal calculus | O/E: uric acid renal calculus | Uric acid renal calculus &/or O/E (finding) | Uric acid renal calculus | Uric acid renal calculus (disorder) | Uric acid nephrolithiasis
+BMGC_DS06908,BMG_DS024961,,Functional Gastrointestinal Disorders,Gastrointestinal Diseases,,,,,,C0559031,D005767,,,,
+BMGC_DS06909,BMG_DS024971,,,,,,,DOID:7806,adult spinal cord glioblastoma multiforme,C0559185,,,MONDO:0004363,adult spinal cord glioblastoma,
+BMGC_DS06910,BMG_DS024992,,,,,,,DOID:4164,cerebral neuroblastoma,C0559458,,,MONDO:0002900,cerebral neuroblastoma,
+BMGC_DS06911,BMG_DS024994,,,,,,,DOID:5718,adrenal neuroblastoma,C0559460,,,MONDO:0006076,adrenal gland neuroblastoma,
+BMGC_DS06912,BMG_DS024995,91930004,Allergy to eggs,,,,,DOID:4377,egg allergy,C0559469,,,,,Allergy to eggs | Allergy to edible egg (finding) | Allergy to edible egg
+BMGC_DS06913,BMG_DS024996,91935009,Allergy to peanuts,,,,,DOID:4378,peanut allergy,C0559470,,,,,Allergy to peanuts | Allergy to peanut | Allergy to peanut (finding)
+BMGC_DS06914,BMG_DS024997,281587000,Pentalogy of Cantrell,Pentalogy of Cantrell,,,,,,C0559483,D058502,313850,MONDO:0010742,pentalogy of Cantrell,Pentalogy of Cantrell | Pentalogy of Cantrell (disorder)
+BMGC_DS06915,BMG_DS025021,282784007,Spinal cord syndrome,,,,,DOID:1089,tethered spinal cord syndrome,C0560648,,,,,Spinal cord syndrome | Spinal cord syndrome (disorder)
+BMGC_DS06916,BMG_DS025045,,,,,,,DOID:6126,anal canal carcinoma,C0563211,,105580,MONDO:0007108,anal canal carcinoma,
+BMGC_DS06917,BMG_DS025046,285344007,Viral gastritis,,,,,DOID:2327,viral gastritis,C0563238,,,MONDO:0002270,viral gastritis,Viral gastritis | Viral gastritis (disorder)
+BMGC_DS06918,BMG_DS025047,285381006,Acute infective exacerbation of chronic obstructive pulmonary disease,,,,,,,C0563269,,,,,Acute infective exacerbation of chronic obstructive airways disease | Acute infective exacerbation of chronic obstructive pulmonary disease | Acute infective exacerbation of chronic obstructive pulmonary disease (disorder)
+BMGC_DS06919,BMG_DS025151,157038006;288250001,Maternal hypertension,,,,,,,C0565599,,,,,Maternal hypertension | Maternal hypertension (disorder)
+BMGC_DS06920,BMG_DS025163,197441003;4032000,Primary sclerosing cholangitis,,,,K83.01,DOID:0060643,primary sclerosing cholangitis,C0566602,,613806,MONDO:0013433,primary sclerosing cholangitis,Primary sclerosing cholangitis | PSC - Primary sclerosing cholangitis | Primary sclerosing cholangitis (disorder) | Primary sclerosing cholangitis | Primary sclerosing cholangitis (disorder)
+BMGC_DS06921,BMG_DS025206,293621000,Allergy to ketoprofen,,,,,DOID:0040060,ketoprofen photoallergic dermatitis,C0570547,,,,,Ketoprofen allergy | Allergy to ketoprofen (finding) | Allergy to ketoprofen
+BMGC_DS06922,BMG_DS025751,294186000,Benzoic acid allergy,,,,,DOID:0040057,benzoic acid allergic contact dermatitis,C0571102,,,,,Benzoic acid allergy | Benzoic acid allergy (disorder)
+BMGC_DS06923,BMG_DS025980,294426006,Allergy to formaldehyde,,,,,DOID:0040074,formaldehyde allergic contact dermatitis,C0571339,,,,,Formaldehyde allergy | Allergy to formaldehyde | Allergy to formaldehyde (finding)
+BMGC_DS06924,BMG_DS026054,,,,,,,DOID:0040021,cephalosporin allergy,C0571444,,,,,
+BMGC_DS06925,BMG_DS026063,294541008,Allergy to cefaclor,,,,,DOID:0040023,cefaclor allergy,C0571453,,,,,Cefaclor allergy | Allergy to cefaclor (finding) | Allergy to cefaclor
+BMGC_DS06926,BMG_DS026064,294542001,Allergy to cefuroxime,,,,,DOID:0040025,cefuroxime allergy,C0571454,,,,,Cefuroxime allergy | Allergy to cefuroxime (finding) | Allergy to cefuroxime
+BMGC_DS06927,BMG_DS026067,294545004,Allergy to cefotaxime,,,,,DOID:0040020,cefotaxime allergy,C0571457,,,,,Cefotaxime allergy | Allergy to cefotaxime (finding) | Allergy to cefotaxime
+BMGC_DS06928,BMG_DS026068,294546003,Allergy to ceftazidime,,,,,DOID:0040024,ceftazidime allergy,C0571458,,,,,Ceftazidime allergy | Allergy to ceftazidime (finding) | Allergy to ceftazidime
+BMGC_DS06929,BMG_DS026070,294548002,Allergy to cefixime,,,,,DOID:0040030,cefixime allergy,C0571460,,,,,Cefixime allergy | Allergy to cefixime | Allergy to cefixime (finding)
+BMGC_DS06930,BMG_DS026073,294551009,Allergy to ceftriaxone,,,,,DOID:0040005,ceftriaxone allergy,C0571463,,,,,Ceftriaxone allergy | Allergy to ceftriaxone | Allergy to ceftriaxone (finding)
+BMGC_DS06931,BMG_DS026621,124239003,Guanidinoacetate methyltransferase deficiency,,,,,DOID:0050799,guanidinoacetate methyltransferase deficiency,C0574080,C537622,612736,MONDO:0012999,guanidinoacetate methyltransferase deficiency,Deficiency of guanidinoacetate methyltransferase | Guanidinoacetate methyltransferase deficiency | Deficiency of guanidinoacetate methyltransferase (disorder)
+BMGC_DS06932,BMG_DS026622,297231002,3-Methylglutaconic aciduria type 2,,,,,DOID:0050476,Barth syndrome,C0574083,,302060,MONDO:0010543,Barth syndrome,3-Methylglutaconic aciduria type 2 | Barth syndrome | 3-Methylglutaconic aciduria type 2 (disorder)
+BMGC_DS06933,BMG_DS026623,297232009,3-Methylglutaconic aciduria type 3,,,,,,,C0574084,,258501,MONDO:0009787,3-methylglutaconic aciduria type 3,Costeff syndrome | 3-Methylglutaconic aciduria type 3 | 3-Methylglutaconic aciduria type 3 (disorder)
+BMGC_DS06934,BMG_DS026625,297237003,Generalized uridine diphosphate galactose-4-epimerase deficiency,,,,,,,C0574089,,,MONDO:0017692,generalized galactose epimerase deficiency,Generalized uridine diphosphate galactose-4-epimerase deficiency | Generalised uridine diphosphate galactose-4-epimerase deficiency | Generalized uridine diphosphate galactose-4-epimerase deficiency (disorder)
+BMGC_DS06935,BMG_DS026626,297238008,Erythrocyte uridine diphosphate galactose-4-epimerase deficiency,,,,,,,C0574090,,,MONDO:0017691,erythrocyte galactose epimerase deficiency,Erythrocyte uridine diphosphate galactose-4-epimerase deficiency | Erythrocyte uridine diphosphate galactose-4-epimerase deficiency (disorder)
+BMGC_DS06936,BMG_DS026631,297256008,Glycerol kinase deficiency - isolated,,,,,DOID:0060363,glycerol kinase deficiency,C0574108,,,MONDO:0018459,isolated glycerol kinase deficiency,Glycerol kinase deficiency - isolated | Glycerol kinase deficiency - isolated (disorder)
+BMGC_DS06937,BMG_DS026647,,"Lesion, Superficial Radial Nerve",Radial Neuropathy,,,,,,C0574908,D020425,,,,
+BMGC_DS06938,BMG_DS026657,55146009;274136001;156620004,Sacroiliitis,Sacroiliitis,,,,,,C0574960,D058566,MTHU021208,,,Sacroiliitis | Inflammation of sacroiliac joint | Sacroiliac joint inflamed | Inflammation of sacroiliac joint (finding) | Sacroiliitis | Sacroiliitis (disorder)
+BMGC_DS06939,BMG_DS026660,298282001,Spastic tetraparesis,,,,,,,C0575059,,MTHU004059,,,Spastic quadriparesis (disorder) | Spastic quadriparesis | Spastic tetraparesis
+BMGC_DS06940,BMG_DS026666,,,,,,,,,C0575897,,188100,MONDO:0008561,thumb deformity,
+BMGC_DS06941,BMG_DS026673,,Nut Hypersensitivity,Nut Hypersensitivity,,,,DOID:4379,nut allergy,C0577620,D021184,,MONDO:0006872,obsolete nut allergic reaction,
+BMGC_DS06942,BMG_DS026679,,,,,,,,,C0577628,,,MONDO:0000807,latex allergy,
+BMGC_DS06943,BMG_DS026682,,Carotid Atherosclerosis,Carotid Artery Diseases,,,,,,C0577631,D002340,,,,
+BMGC_DS06944,BMG_DS026693,300986008,Proteus septicemia,,,,,,,C0577690,,,,,Proteus septicemia | Proteus septicaemia | Proteus septicemia (disorder)
+BMGC_DS06945,BMG_DS026694,,,,,,,DOID:6888,ureter transitional cell carcinoma,C0577692,,,MONDO:0004030,ureter transitional cell carcinoma,
+BMGC_DS06946,BMG_DS026698,301011002,Urinary tract infection caused by Escherichia coli,,,,,,,C0577708,,,,,Escherichia coli urinary tract infection | Urinary tract infection caused by Escherichia coli | Urinary tract infection caused by Escherichia coli (disorder)
+BMGC_DS06947,BMG_DS026699,301012009,Proteus urinary tract infection,,,,,,,C0577709,,,,,Proteus urinary tract infection | Proteus urinary tract infection (disorder) | Proteus UTI (urinary tract infection)
+BMGC_DS06948,BMG_DS026730,301990003,Gonococcal seminal vesiculitis,,,,,DOID:10400;DOID:0050004,gonococcal seminal vesiculitis | seminal vesicle acute gonorrhea,C0578661,,,MONDO:0001027,gonococcal seminal vesiculitis,Gonococcal seminal vesiculitis | Gonococcal seminal vesiculitis (disorder)
+BMGC_DS06949,BMG_DS026738,,Chronic Spontaneous Urticaria,Chronic Urticaria,,,,DOID:0080747,chronic urticaria,C0578870,D000080223,,MONDO:0044212,chronic idiopathic urticaria,
+BMGC_DS06950,BMG_DS026743,302168000,Inflammation of large intestine,,,,,,,C0578878,,,,,Inflammation of large intestine | Inflammation of large intestine (disorder)
+BMGC_DS06951,BMG_DS026784,195788001,Recurrent sinusitis,,,,,,,C0581354,,MTHU008465,,,Recurrent sinusitis | Recurrent sinusitis (disorder)
+BMGC_DS06952,BMG_DS026802,195111005,Decompensated cardiac failure,,,,,,,C0581377,,,,,Decompensated cardiac failure | Decompensated cardiac failure (disorder)
+BMGC_DS06953,BMG_DS026804,195708003,Recurrent upper respiratory tract infection,,,,,,,C0581381,,,,,Recurrent upper respiratory tract infection | Recurrent upper respiratory tract infection (disorder)
+BMGC_DS06954,BMG_DS026808,192929006,Exacerbation of multiple sclerosis,,,,,,,C0581392,,,,,Exacerbation of multiple sclerosis | Exacerbation of multiple sclerosis (disorder) | Multiple sclerosis (MS) exacerbation
+BMGC_DS06955,BMG_DS026809,,Complete Hearing Loss,Deafness,,,,,,C0581883,D003638,,,,
+BMGC_DS06956,BMG_DS026860,,,,,,,DOID:12341,retroperitoneal sarcoma,C0585129,,,MONDO:0001501,retroperitoneal sarcoma,
+BMGC_DS06957,BMG_DS026863,307227006,Gastric retention,,,,,,,C0585136,,,,,Gastric retention | Gastric retention (disorder)
+BMGC_DS06958,BMG_DS026874,,,,,,,DOID:0112125,alpha-thalassemia myelodysplasia syndrome,C0585216,,300448,MONDO:0010328,alpha-thalassemia-myelodysplastic syndrome,
+BMGC_DS06959,BMG_DS026885,,Hypoglossal Nerve Palsy,Hypoglossal Nerve Diseases,,,,,,C0585265,D020437,,,,
+BMGC_DS06960,BMG_DS026889,,,,,,,,,C0585362,,,MONDO:0004958,oral cavity squamous cell carcinoma,
+BMGC_DS06961,BMG_DS026894,,,,,,,DOID:3376,bone osteosarcoma,C0585442,,259500,MONDO:0002629,bone osteosarcoma,
+BMGC_DS06962,BMG_DS026895,,,,,,,DOID:3368,Ewing sarcoma of bone,C0585474,,,MONDO:0002625,Ewing sarcoma of bone,
+BMGC_DS06963,BMG_DS026896,,,,,,,DOID:5376,skin pilomatrix carcinoma,C0585475,,,MONDO:0003414,skin pilomatrix carcinoma,
+BMGC_DS06964,BMG_DS026917,,,,,,,DOID:8133,epiglottis cancer,C0585946,,,,,
+BMGC_DS06965,BMG_DS026926,,Alcohol Withdrawal Seizures,Alcohol Withdrawal Seizures,,,,,,C0586323,D020270,,,,
+BMGC_DS06966,BMG_DS026958,,Varicella Zoster Virus Infection,Varicella Zoster Virus Infection,,,,,,C0586989,D000073618,,MONDO:0005608,varicella zoster infection,
+BMGC_DS06967,BMG_DS026972,205803001;309776008,Costello syndrome (disorder),,,,,DOID:0050469,Costello syndrome,C0587248,,218040,MONDO:0009026,Costello syndrome,Costello syndrome | Costello syndrome (disorder)
+BMGC_DS06968,BMG_DS026975,,,,,,,DOID:2701,nodular tenosynovitis,C0588125,,,MONDO:0002399,"tenosynovial giant cell tumor, localized type",
+BMGC_DS06969,BMG_DS026982,186383002;310669007,Septicemia due to enterococcus,,,,,,,C0588233,,,,,Septicemia due to enterococcus | Septicaemia due to enterococcus | Septicaemia due to enterococcus (disorder) | Septicaemia due to enterococcus | Septicemia due to enterococcus | Sepsis due to enterococcus | Septicemia caused by enterococcus | Septicemia caused by enterococcus (disorder) | Sepsis caused by enterococcus | Septicaemia caused by enterococcus
+BMGC_DS06970,BMG_DS027011,23374007,Atypical absence seizure,,,,,,,C0595948,,,,,Atypical absence seizure | Atypical absence seizure (finding)
+BMGC_DS06971,BMG_DS027020,,,,,,,DOID:2600,laryngeal carcinoma,C0595989,,,MONDO:0002358,laryngeal carcinoma,
+BMGC_DS06972,BMG_DS027022,,,,,,,,,C0595995,,,MONDO:0000726,idiopathic scoliosis,
+BMGC_DS06973,BMG_DS027024,,,,,,,DOID:5719,adrenal medulla cancer,C0596046,,,MONDO:0021237,adrenal medulla neoplasm,
+BMGC_DS06974,BMG_DS027025,,,,,,,,,C0596170,,,MONDO:0005582,binge eating disorder,
+BMGC_DS06975,BMG_DS027027,,Cerebrovascular Occlusion,Cerebrovascular Disorders,,,,,,C0596298,D002561,,,,
+BMGC_DS06976,BMG_DS027030,,,,,,,DOID:10619,lymph node cancer,C0596869,,,MONDO:0024339,lymph node neoplasm,
+BMGC_DS06977,BMG_DS027036,439274008,Hereditary protein C deficiency,,,,,,,C0598221,,,MONDO:0019145,hereditary thrombophilia due to congenital protein C deficiency,Hereditary protein C deficiency (disorder) | Hereditary protein C deficiency
+BMGC_DS06978,BMG_DS027037,,Harlequin type ichthyosis,,,,,,,C0598226,C538424,242500,MONDO:0009443,autosomal recessive congenital ichthyosis 4B,
+BMGC_DS06979,BMG_DS027039,419503008,Hyperhomocysteinemia,Hyperhomocysteinemia,,,,DOID:9279,hyperhomocysteinemia,C0598608,D020138,MTHU070462;603174,MONDO:0004743,hyperhomocysteinemia,Hyperhomocysteinemia (disorder) | Hyperhomocysteinemia
+BMGC_DS06980,BMG_DS027041,,,,,,,DOID:2784,lung sarcoma,C0598790,,,MONDO:0002426,lung sarcoma,
+BMGC_DS06981,BMG_DS027042,,,,,,,DOID:0060058,lymphoma,C0598798,,,MONDO:0005157,lymphoid neoplasm,
+BMGC_DS06982,BMG_DS027044,33985005,Hyperornithinemia,,,,,,,C0599035,,MTHU023295,,,Hyperornithinemia | Hyperornithinaemia | Hyperornithinemia (disorder)
+BMGC_DS06983,BMG_DS027047,,,,,,,,,C0599973,,206920,MONDO:0008800,microphthalmia with limb anomalies,
+BMGC_DS06984,BMG_DS027048,44497007;197834003,Chronic interstitial cystitis,,,,,DOID:1678,chronic interstitial cystitis,C0600040,,,,,Chronic interstitial cystitis | Chronic interstitial cystitis (disorder) | Chronic interstitial cystitis | IC - Interstitial cystitis | Interstitial cystitis | Chronic interstitial cystitis (disorder) | PBS - Painful bladder syndrome | Painful bladder syndrome
+BMGC_DS06985,BMG_DS027049,236620008,Infective cystitis,,,,,,,C0600041,,,,,Infective cystitis | Infection of bladder | Infective cystitis (disorder)
+BMGC_DS06986,BMG_DS027051,,,,,,,DOID:3016,breast malignant phyllodes tumor,C0600066,,,MONDO:0037003,malignant phyllodes tumor,
+BMGC_DS06987,BMG_DS027052,,,,,,,DOID:4939,ureter carcinoma,C0600079,,,MONDO:0006481,ureter carcinoma,
+BMGC_DS06988,BMG_DS027057,,,,,,,DOID:10286,prostate carcinoma,C0600139,,,MONDO:0005159,prostate carcinoma,
+BMGC_DS06989,BMG_DS027058,,External Carotid Artery Diseases,Carotid Artery Diseases,,,,,,C0600178,D002340,,,,
+BMGC_DS06990,BMG_DS027059,,,,,,,DOID:0060319,cardiac arrest,C0600228,,,,,
+BMGC_DS06991,BMG_DS027060,,"Lung Diseases, Obstructive","Lung Diseases, Obstructive",,,,DOID:2320,obstructive lung disease,C0600260,D008173,,,,
+BMGC_DS06992,BMG_DS027063,,Periodontosis,Aggressive Periodontitis,DA0C.2,Periodontosis,K05.4,DOID:9893,periodontosis,C0600298,D010520,,,,
+BMGC_DS06993,BMG_DS027064,,Toxic Shock Syndrome,"Shock, Septic",,,,DOID:14115,toxic shock syndrome,C0600327,D012772,,MONDO:0001881,toxic shock syndrome,
+BMGC_DS06994,BMG_DS027065,25147002,Subcorneal pustular dermatosis,,,,,DOID:8508,subcorneal pustular dermatosis,C0600336,,,MONDO:0006614,subcorneal pustular dermatosis,Subcorneal pustular dermatosis | Sneddon-Wilkinson disease | Sneddon-Wilkinson syndrome | Subcorneal pustular dermatosis (disorder)
+BMGC_DS06995,BMG_DS027066,,Arteriosclerotic Dementia,"Dementia, Vascular",,,,,,C0600359,D015140,,,,
+BMGC_DS06996,BMG_DS027067,,,,,,,DOID:9975,cocaine dependence,C0600427,,,MONDO:0005186,cocaine dependence,
+BMGC_DS06997,BMG_DS027068,,Activated Protein C Resistance,Activated Protein C Resistance,,,,,,C0600433,D020016,,,,
+BMGC_DS06998,BMG_DS027069,,Hepatopulmonary Syndrome,Hepatopulmonary Syndrome,,,,DOID:900,hepatopulmonary syndrome,C0600452,D020065,,MONDO:0004694,hepatopulmonary syndrome,
+BMGC_DS06999,BMG_DS027070,,Vascular Hemostatic Disorders,Hemostatic Disorders,,,,DOID:484,vascular hemostatic disease,C0600502,D020141,,MONDO:0003159,vascular hemostatic disease,
+BMGC_DS07000,BMG_DS027072,,,,,,,,,C0600518,,,MONDO:0810000,choroidal neovascularization,
+BMGC_DS07001,BMG_DS027074,,,,,,,DOID:1294,vulva carcinoma,C0677055,,,MONDO:0005215,vulvar carcinoma,
+BMGC_DS07002,BMG_DS027076,,Radial Tunnel Syndrome,Radial Neuropathy,,,,,,C0677499,D020425,,,,
+BMGC_DS07003,BMG_DS027077,,Congenital Nephrogenic Diabetes Insipidus,"Diabetes Insipidus, Nephrogenic",,,,,,C0677501,D018500,,,,
+BMGC_DS07004,BMG_DS027079,,Hashimoto Disease,Hashimoto Disease,,,,,,C0677607,D050031,140300,MONDO:0007699,Hashimoto thyroiditis,
+BMGC_DS07005,BMG_DS027081,266433003,Gastro-esophageal reflux disease with esophagitis,,DA22.Z,"Gastrooesophageal reflux disease, unspecified",K21.0,,,C0677659,,,,,Reflux esophagitis | Esophageal reflux with esophagitis | Gastro-esophageal reflux disease with esophagitis | Gastro-oesophageal reflux disease with oesophagitis | Oesophageal reflux with oesophagitis | Reflux oesophagitis | Gastroesophageal reflux disease with esophagitis (disorder) | Gastroesophageal reflux disease with esophagitis | Gastroesophageal reflux disease with oesophagitis | Peptic esophagitis | Peptic oesophagitis
+BMGC_DS07006,BMG_DS027082,,,,,,,DOID:5683,hereditary breast ovarian cancer syndrome,C0677776,,,MONDO:0003582,hereditary breast ovarian cancer syndrome,
+BMGC_DS07007,BMG_DS027083,,,,,,,DOID:5183,hereditary Wilms' tumor,C0677779,,,MONDO:0003321,hereditary Wilms tumor,
+BMGC_DS07008,BMG_DS027084,,,,,,,DOID:4202,brain stem glioma,C0677865,,,MONDO:0002911,brain stem glioma,
+BMGC_DS07009,BMG_DS027085,,,,,,,DOID:4203,brain stem cancer,C0677866,,,MONDO:0021228,brainstem neoplasm,
+BMGC_DS07010,BMG_DS027086,,,,,,,DOID:4001,ovarian carcinoma,C0677886,,,,,
+BMGC_DS07011,BMG_DS027091,190774002,"Hyperlipidemia, group A",,,,,,,C0678189,,,,,"Hyperlipidemia, group A | Hyperlipidaemia, group A | Hyperlipidemia, group A (disorder)"
+BMGC_DS07012,BMG_DS027092,,Terminal Ileitis,Crohn Disease,,,,,,C0678201,D003424,,,,
+BMGC_DS07013,BMG_DS027093,278522007;266517004;155760003,Regional enteritis,,,,,,,C0678202,,MTHU054371,,,Regional enteritis | Regional enteritis (disorder) | Regional enteritis - Crohn | Enteritis - regional | Regional enteritis | Crohn's disease | Crohn's regional enteritis | Crohn's disease (& [regional enteritis]) | Crohn's disease (& [regional enteritis]) (disorder) | Crohn's regional enteritis | Enteritis - regional | Regional enteritis - Crohn | Crohn's disease | Regional enteritis | Crohn's disease (& [regional enteritis]) | Crohn's disease (& [regional enteritis]) (disorder)
+BMGC_DS07014,BMG_DS027094,,,,,,,,,C0678213,,,MONDO:0016785,complete hydatidiform mole,
+BMGC_DS07015,BMG_DS027095,,,,,,,DOID:3459,breast carcinoma,C0678222,,,MONDO:0004989,breast carcinoma,
+BMGC_DS07016,BMG_DS027099,,"Tuberculosis, Extrapulmonary","Tuberculosis, Extrapulmonary",,,,,,C0679362,D000092225,,MONDO:0000368,extrapulmonary tuberculosis,
+BMGC_DS07017,BMG_DS027104,,,,,,,DOID:11038,depersonalization disorder,C0683416,,,MONDO:0001186,depersonalization disorder,
+BMGC_DS07018,BMG_DS027105,,,,,,,DOID:3905,lung carcinoma,C0684249,,,MONDO:0005138,lung carcinoma,
+BMGC_DS07019,BMG_DS027106,10001005,Bacterial sepsis,,,,,,,C0684256,,,,,Bacterial septicemia | Bacterial sepsis | Bacterial septicaemia | Bacterial sepsis (disorder)
+BMGC_DS07020,BMG_DS027107,90935002,"Hemophilia, NOS",,,,,,,C0684275,,,MONDO:0018660,hemophilia,Hemophilia | Haemophilia | Hemophilia (disorder)
+BMGC_DS07021,BMG_DS027109,,,,,,,DOID:8649,tongue cancer,C0684333,,,,,
+BMGC_DS07022,BMG_DS027110,,,,,,,DOID:3369,Ewing sarcoma,C0684337,,,MONDO:0018271,peripheral primitive neuroectodermal tumor,
+BMGC_DS07023,BMG_DS027118,,,,,,,DOID:4045,muscle cancer,C0684743,,,MONDO:0005864,muscle cancer,
+BMGC_DS07024,BMG_DS027148,,,,,,,DOID:13081,hemangioma of subcutaneous tissue,C0685200,,,MONDO:0006557,hemangioma of subcutaneous tissue,
+BMGC_DS07025,BMG_DS027149,,,,,,,DOID:256,hemangioma of spleen,C0685201,,,MONDO:0002343,splenic hemangioma,
+BMGC_DS07026,BMG_DS027163,,,,,,,,,C0685787,,,MONDO:0015411,facial cleft,
+BMGC_DS07027,BMG_DS027164,,,,,,,,,C0685837,,,MONDO:0009299,46 XX gonadal dysgenesis,
+BMGC_DS07028,BMG_DS027165,,Gonadal dysgenesis XX type deafness,,,,,,,C0685838,C537286,,MONDO:0017312,Perrault syndrome,
+BMGC_DS07029,BMG_DS027166,,,,,,,,,C0685889,,271400,MONDO:0010066,familial isolated congenital asplenia,
+BMGC_DS07030,BMG_DS027194,,,,,,,DOID:3119,gastrointestinal system cancer,C0685938,,,,,
+BMGC_DS07031,BMG_DS027206,,Tardive Dyskinesia,Tardive Dyskinesia,,,,,,C0686347,D000071057,272620,MONDO:0010096,tardive dyskinesia,
+BMGC_DS07032,BMG_DS027211,,"Muscular Dystrophies, Limb-Girdle","Muscular Dystrophies, Limb-Girdle",,,,DOID:11724,limb-girdle muscular dystrophy,C0686353,D049288,,MONDO:0016971,limb-girdle muscular dystrophy,
+BMGC_DS07033,BMG_DS027221,41446000;92819001,Marginal blepharitis,,,,,,,C0686366,,,,,Blepharitis | Blepharitis (disorder) | Inflammation of lid margin | Marginal blepharitis | Marginal blepharitis | Ciliary blepharitis | Marginal blepharitis (disorder)
+BMGC_DS07034,BMG_DS027230,,,,,,,DOID:2816,malignant oculomotor nerve tumor,C0686417,,,MONDO:0002434,oculomotor nerve cancer,
+BMGC_DS07035,BMG_DS027253,204958008,Nephronophthisis,,GB82,Autosomal dominant tubulointerstitial disease,Q61.5,DOID:12712,nephronophthisis,C0687120,,MTHU000621,MONDO:0019005,nephronophthisis,Nephronophthisis | Familial juvenile medullary cystic kidney disease | Autosomal recessive medullary cystic disease | Nephronophthisis (disorder) | Familial juvenile nephronophthisis
+BMGC_DS07036,BMG_DS027254,,,,,,,DOID:471,skin hemangioma,C0687140,,,MONDO:0003110,skin hemangioma,
+BMGC_DS07037,BMG_DS027255,367101009;111379007,Mineral deficiency,,,,,,,C0687148,,,,,Mineral deficiency | Mineral deficiency (disorder)
+BMGC_DS07038,BMG_DS027256,,,,,,,DOID:1540,parathyroid carcinoma,C0687150,,608266,MONDO:0012004,parathyroid gland carcinoma,
+BMGC_DS07039,BMG_DS027257,205257004;205260006,Acrocephalopolysyndactyly,,LD2Z,"Multiple developmental anomalies or syndromes, unspecified",Q87.0,DOID:0110716;DOID:0110719;DOID:0110718;DOID:0110717,Warburg micro syndrome 3 | Warburg micro syndrome 1 | Warburg micro syndrome 2 | Warburg micro syndrome 4,C0687154,,,MONDO:0000078,acrocephalopolysyndactyly,(Acrocephalo (& [poly]) syndactyly) or (Apert's syndrome) | Acrocephalosyndactyly | Acrocephalopolysyndactyly | Apert's syndrome | (Acrocephalo (& [poly]) syndactyly) or (Apert's syndrome) (disorder) | Acrocephalopolysyndactyly | Acrocephalopolysyndactyly (disorder)
+BMGC_DS07040,BMG_DS027259,,Central Diabetes Insipidus,"Diabetes Insipidus, Neurogenic",,,,DOID:12388,neurohypophyseal diabetes insipidus,C0687720,D020790,,MONDO:0015790,central diabetes insipidus,
+BMGC_DS07041,BMG_DS027260,250249008;83123000,Acanthocytosis,,,,,,,C0687751,,MTHU014873,,,Spiny prickle cells present | Acanthocytosis | Acanthocytosis (finding) | Abetalipoproteinemia | Abetalipoproteinaemia | Abetalipoproteinemia (disorder)
+BMGC_DS07042,BMG_DS027288,,Community-Acquired Pneumonia,Community-Acquired Pneumonia,,,,,,C0694549,D000098968,,,,
+BMGC_DS07043,BMG_DS027291,240413000,Disseminated atypical mycobacterial infection,,,,,,,C0694566,,,,,Disseminated atypical mycobacterial infection | Disseminated atypical mycobacterial infection (disorder)
+BMGC_DS07044,BMG_DS027292,,Neurogenic Bowel,Neurogenic Bowel,,,,DOID:13419,neurogenic bowel,C0695242,D055496,,MONDO:0006868,neurogenic bowel,
+BMGC_DS07045,BMG_DS027293,,Hereditary Chorea,Chorea,,,,,,C0699731,D002819,,,,
+BMGC_DS07046,BMG_DS027295,,"Sensory Neuropathy, Hereditary",Hereditary Sensory and Autonomic Neuropathies,,,,DOID:0050548;DOID:2491,hereditary sensory neuropathy | sensory peripheral neuropathy,C0699739,D009477,,,,
+BMGC_DS07047,BMG_DS027296,193222002;111501005,Benign congenital myopathy,,,,,DOID:9883,Becker muscular dystrophy,C0699741,,,,,Benign congenital myopathy | Benign congenital myopathy (disorder) | Congenital hereditary muscular dystrophy | Congenital hereditary muscular dystrophy (disorder)
+BMGC_DS07048,BMG_DS027297,240059009,Congenital muscular dystrophy (disorder),,,,,,,C0699743,,,MONDO:0019950,congenital muscular dystrophy,Congenital muscular dystrophy | Congenital muscular dystrophy (disorder)
+BMGC_DS07049,BMG_DS027298,129127001,Infection of ear,,,,,,,C0699744,,,MONDO:0021666,ear infection,Ear infection | Infection of ear | Infection of ear (disorder)
+BMGC_DS07050,BMG_DS027299,,,,,,,DOID:1520,colon carcinoma,C0699790,,,MONDO:0002032,colon carcinoma,
+BMGC_DS07051,BMG_DS027300,,,,,,,DOID:5517,stomach carcinoma,C0699791,,,MONDO:0004950,gastric carcinoma,
+BMGC_DS07052,BMG_DS027301,,,,,,,,,C0699828,,,MONDO:0018546,serotonin syndrome,
+BMGC_DS07053,BMG_DS027304,,,,,,,DOID:4007,bladder carcinoma,C0699885,,,MONDO:0004986,urinary bladder carcinoma,
+BMGC_DS07054,BMG_DS027305,,,,,,,DOID:120,female reproductive organ cancer,C0699889,,,MONDO:0001416,female reproductive organ cancer,
+BMGC_DS07055,BMG_DS027307,,,,,,,DOID:3451,skin carcinoma,C0699893,,,MONDO:0002656,skin carcinoma,
+BMGC_DS07056,BMG_DS027309,83497002;360465008,Idiopathic hypertrophic subaortic stenosis,,,,,,,C0700053,,,,,Idiopathic hypertrophic subaortic stenosis | Idiopathic hypertrophic subaortic stenosis (disorder)
+BMGC_DS07057,BMG_DS027311,,,,,,,DOID:734,urethra cancer,C0700101,,,,,
+BMGC_DS07058,BMG_DS027312,,,,,,,DOID:2762,bone carcinoma,C0700110,,,MONDO:0024884,metastatic carcinoma in the bone,
+BMGC_DS07059,BMG_DS027317,66071002,Viral hepatitis B without mention of hepatic coma,,,,,,,C0700211,,,,,Type B viral hepatitis | Serum hepatitis | Hepatitis B | SH - Serum hepatitis | Hepatitis B infection | Viral hepatitis type B | Viral hepatitis type B (disorder)
+BMGC_DS07060,BMG_DS027318,186342000;373435003;14009004,Pulmonary mycobacterium avium-intracellulare infection,,,,,,,C0700226,,,,,Pulmonary Mycobacterium avium complex infection (disorder) | Pulmonary Mycobacterium avium complex infection | Pulmonary Mycobacterium avium-intracellulare infection | Battey disease (disorder) | Battey disease | Pulmonary mycobacterium intracellulare infection | Battey disease | Battey disease (disorder)
+BMGC_DS07061,BMG_DS027319,,Brachial Plexus Neuropathies,Brachial Plexus Neuropathies,,,,DOID:3690,brachial plexus neuropathy,C0700251,D020516,,MONDO:0006683,brachial plexus neuropathy,
+BMGC_DS07062,BMG_DS027320,,Heinz Body Anemias,,,,,,,C0700299,C563030,140700,MONDO:0007705,Heinz body anemia,
+BMGC_DS07063,BMG_DS027321,89155008,Thibierge-Weissenbach syndrome,,,,,,,C0700318,,,,,Systemic sclerosis | Systemic scleroderma | Thibierge-Weissenbach syndrome | SS - Systemic sclerosis | Systemic sclerosis (disorder)
+BMGC_DS07064,BMG_DS027323,,"Candidiasis, Vulvovaginal","Candidiasis, Vulvovaginal",,,,DOID:2272,vulvovaginal candidiasis,C0700345,D002181,,MONDO:0006014,vulvovaginal candidiasis,
+BMGC_DS07065,BMG_DS027325,,,,,,,DOID:0080903,"embryonal tumor with multilayered rosettes, C19MC-altered",C0700367,,,MONDO:0016715,ependymoblastoma,
+BMGC_DS07066,BMG_DS027327,,Sick Headaches,Migraine Disorders,,,,,,C0700438,D008881,,,,
+BMGC_DS07067,BMG_DS027329,,,,,,,DOID:9649,congenital nystagmus,C0700501,,,MONDO:0005712,congenital nystagmus,
+BMGC_DS07068,BMG_DS027332,128287004,Chronic peptic ulcer,,,,,,,C0700509,,,,,Chronic peptic ulcer | Chronic peptic ulcer (disorder)
+BMGC_DS07069,BMG_DS027335,,,,,,,DOID:14099,acquired gastric outlet stenosis,C0700588,,,MONDO:0001878,acquired hypertrophic pyloric stenosis,
+BMGC_DS07070,BMG_DS027336,394640000;72274001,Radiculopathy,Radiculopathy,8B93.Z,"Radiculopathy, unspecified",M54.1,DOID:4306,radiculopathy,C0700594,D011843,,MONDO:0002959,radiculopathy,Radiculopathy | Nerve root disorder | Radiculopathy (disorder) | Nerve root disorder | Radiculopathy | Nerve root disorder (disorder)
+BMGC_DS07071,BMG_DS027337,,Spinal Muscular Atrophies of Childhood,Spinal Muscular Atrophies of Childhood,,,,DOID:0060160,childhood spinal muscular atrophy,C0700595,D014897,,,,
+BMGC_DS07072,BMG_DS027339,702350003,Strudwick syndrome,,,,,,,C0700635,C537501,184250,MONDO:0008476,"spondyloepimetaphyseal dysplasia, Strudwick type","Dappled metaphysis syndrome | Spondyloepimetaphyseal dysplasia, Strudwick type | Spondyloepimetaphyseal dysplasia, Strudwick type (disorder) | SEMD - spondyloepimetaphyseal dysplasia, Strudwick type | Strudwick syndrome"
+BMGC_DS07073,BMG_DS027342,,,,,,,DOID:12638,hypertrophic pyloric stenosis,C0700639,,,MONDO:0100239,inherited hypertrophic pyloric stenosis,
+BMGC_DS07074,BMG_DS027350,154706003;267395000,Adrenogenital disorder,,,,,DOID:0050811,congenital adrenal hyperplasia,C0701163,,,,,Adrenogenital disorder | Adrenogenital disorder (disorder) | Adrenogenital disorder | Adrenogenital syndrome | Androgenital syndrome | Adrenogenital disorder (disorder)
+BMGC_DS07075,BMG_DS027353,49910001;197397004,Choledocholithiasis,Choledocholithiasis,,,,DOID:11755,choledocholithiasis,C0701818,D042883,,MONDO:0006699,choledocholithiasis,Calculus of common bile duct | Calculus of common bile duct (disorder) | Bile duct calculus (& [without mention of cholecystitis]) | Bile duct calculus without mention of cholecystitis | Choledocholithiasis | Bile duct calculus (& [without mention of cholecystitis]) (disorder)
+BMGC_DS07076,BMG_DS027355,190303007,Disorder of thyrocalcitonin secretion,,,,,DOID:12424,thyrocalcitonin secretion disease,C0701822,,,MONDO:0001525,thyrocalcitonin secretion disease,Disorder of thyrocalcitonin secretion | Disorder of thyrocalcitonin secretion (disorder)
+BMGC_DS07077,BMG_DS027363,1534008,Palsy of conjugate gaze,,,,,DOID:12445,conjugate gaze palsy,C0702143,,,MONDO:0001527,conjugate gaze palsy,Palsy of conjugate gaze | Conjugate gaze palsy | Palsy of conjugate gaze (disorder)
+BMGC_DS07078,BMG_DS027366,267523003;28975000;191235004;154808006,Constitutional aplastic anemia,,3A9Z,"Anaemias or other erythrocyte disorders, unspecified",D61.0,DOID:1342,congenital hypoplastic anemia,C0702159,,,,,Hypoplastic anaemia - familial | Constitutional aplastic anaemia | Constitutional aplastic anemia | Hypoplastic anemia - familial | Constitutional aplastic anemia (disorder) | Constitutional aplastic anemia | Congenital aplastic anaemia | Constitutional aplastic anaemia | Congenital aplastic anemia | Constitutional aplastic anemia (disorder) | Hypoplastic anaemia - familial | Hypoplastic anemia - familial | Pancytopenia with malformations | Blackfan - Diamond syndrome | (Anemia: [constitutional aplastic] or [familial hypoplastic]) or (pancytopenia with malformations) or (Blackfan - Diamond syndrome) | (Anaemia: [constitutional aplastic] or [familial hypoplastic]) or (pancytopenia with malformations) or (Blackfan - Diamond syndrome) | Constitutional aplastic anemia | Hypoplastic anemia - familial | Constitutional aplastic anaemia | Hypoplastic anaemia - familial | (Anaemia: [constitutional aplastic] or [familial hypoplastic]) or (pancytopenia with malformations) or (Blackfan - Diamond syndrome) (disorder) | Constitutional aplastic anaemia | Constitutional aplastic anemia | Constitutional aplastic anaemia (disorder)
+BMGC_DS07079,BMG_DS027369,11381005,Acne,Acne Vulgaris,,,L70,DOID:6543,acne,C0702166,D000152,MTHU036937,MONDO:0011438,acne,Acne | Acne (disorder)
+BMGC_DS07080,BMG_DS027375,,,,,,,DOID:10811,nasal cavity cancer,C0728864,,,MONDO:0001128,nasal cavity cancer,
+BMGC_DS07081,BMG_DS027376,49601007,Disorder of circulatory system,,,,,,,C0728936,,,,,Cardiovascular disorder | Disorder of circulatory system | Cardiovascular disease | Disorder of the circulatory system | Cardiovascular system disease | Disorder of cardiovascular system (disorder) | Disorder of cardiovascular system | CVD - cardiovascular disease | CVS disease - cardiovascular system disease
+BMGC_DS07082,BMG_DS027378,,,,,,,DOID:4902,appendix carcinoma,C0728951,,,MONDO:0003196,appendix carcinoma,
+BMGC_DS07083,BMG_DS027380,196682000,Acute peptic ulcer (disorder),,,,,,,C0729245,,,,,Acute peptic ulcer | Acute peptic ulcer (disorder)
+BMGC_DS07084,BMG_DS027386,,,,,,,,,C0729264,,610504,MONDO:0012511,preterm premature rupture of the membranes,
+BMGC_DS07085,BMG_DS027393,312117008,Bacterial respiratory infection,,,,,,,C0729518,,,,,Bacterial respiratory infection | Bacterial respiratory infection (disorder)
+BMGC_DS07086,BMG_DS027394,312118003,Bacterial upper respiratory infection,,,,,,,C0729519,,,,,Bacterial upper respiratory infection | Bacterial upper respiratory infection (disorder)
+BMGC_DS07087,BMG_DS027395,312119006,Bacterial lower respiratory infection,,,,,,,C0729520,,,,,Bacterial lower respiratory infection | Bacterial lower respiratory infection (disorder)
+BMGC_DS07088,BMG_DS027399,312124009,Bacterial urinary infection,,,,,,,C0729524,,,MONDO:0005247,bacterial urinary tract infection,Bacterial urinary infection | Bacterial urinary infection (disorder) | Bacterial UTI (urinary tract infection)
+BMGC_DS07089,BMG_DS027410,312137007,Viral ear infection,,,,,,,C0729535,,,,,Viral ear infection | Viral ear infection (disorder)
+BMGC_DS07090,BMG_DS027413,312148000,Fungal ear infection,,,,,,,C0729545,,,,,Fungal ear infection | Fungal ear infection (disorder)
+BMGC_DS07091,BMG_DS027426,,Floating-harbor syndrome,,,,,DOID:0111358,Floating-Harbor syndrome,C0729582,C537062,136140,MONDO:0007621,Floating-Harbor syndrome,
+BMGC_DS07092,BMG_DS027429,312218008,Infective otitis media,,,,,,,C0729586,,,,,Infective otitis media | Infective otitis media (disorder)
+BMGC_DS07093,BMG_DS027430,312219000,Infective blepharitis,,,,,,,C0729587,,,,,Infective blepharitis | Infective blepharitis (disorder)
+BMGC_DS07094,BMG_DS027450,312423006,Infective laryngitis,,,,,,,C0729772,,,,,Infective laryngitis | Infective laryngitis (disorder)
+BMGC_DS07095,BMG_DS027502,312901001,Vitreomacular traction syndrome,,,,,,,C0730274,,,,,Vitreomacular traction syndrome | Vitreomacular traction syndrome (disorder)
+BMGC_DS07096,BMG_DS027506,312905005,Severe nonproliferative diabetic retinopathy,,,,,DOID:8946,severe nonproliferative diabetic retinopathy,C0730278,,,MONDO:0004687,severe nonproliferative diabetic retinopathy,Severe nonproliferative diabetic retinopathy | Severe nonproliferative retinopathy | Severe NPDR (nonproliferative diabetic retinopathy) | Severe nonproliferative retinopathy due to diabetes mellitus (disorder) | Severe nonproliferative retinopathy due to diabetes mellitus
+BMGC_DS07097,BMG_DS027513,312912001,Macular edema due to diabetes mellitus,,,,,DOID:9191,diabetic macular edema,C0730285,,,MONDO:0004728,diabetic macular edema,Diabetic macular edema | Diabetic macular oedema | Macular edema due to diabetes mellitus | Macular edema due to diabetes mellitus (disorder) | Macular oedema due to diabetes mellitus
+BMGC_DS07098,BMG_DS027518,,Cone Dystrophy,Cone Dystrophy,,,,DOID:0050795,cone dystrophy,C0730290,D000077765,,MONDO:0000455,cone dystrophy,
+BMGC_DS07099,BMG_DS027519,312918002,Choroidal dystrophy,,,,,,,C0730291,,MTHU067558,,,Choroidal dystrophy | Choroidal dystrophy (disorder)
+BMGC_DS07100,BMG_DS027520,312919005,Macular dystrophy,,,,,,,C0730292,,MTHU013225,,,Macular dystrophy | Macular dystrophy (disorder)
+BMGC_DS07101,BMG_DS027522,312925009,North Carolina macular dystrophy,,,,,DOID:0070439,North Carolina macular dystrophy,C0730294,,136550,MONDO:0007630,North Carolina macular dystrophy,North Carolina macular dystrophy | North Carolina macular dystrophy (disorder)
+BMGC_DS07102,BMG_DS027523,,,,,,,,,C0730295,,126700,MONDO:0007472,basal laminar drusen,
+BMGC_DS07103,BMG_DS027530,,,,,,,DOID:5240,retinal hemangioblastoma,C0730303,,,MONDO:0003343,retinal hemangioblastoma,
+BMGC_DS07104,BMG_DS027532,,,,,,,DOID:6903,eye lymphoma,C0730306,,,MONDO:0004034,eye lymphoma,
+BMGC_DS07105,BMG_DS027558,312999006,Disorder of macula of retina,,,,,,,C0730362,,,,,Macular disease | Macular disorder | Disorder of macula of retina (disorder) | Disorder of macula of retina | Maculopathy
+BMGC_DS07106,BMG_DS027563,313017000;199655009,Anhydramnios,,,,,,,C0730379,,MTHU041644,,,Anhydramnios | Anhydramnios (disorder)
+BMGC_DS07107,BMG_DS027575,313165001,Functional visual loss,,,,,,,C0730512,,,,,Functional visual loss | Functional visual loss (disorder) | Nonphysiologic vision loss | Nonphysiologic acuity loss
+BMGC_DS07108,BMG_DS027584,195998004;313299006;155584009,Severe chronic obstructive pulmonary disease,,,,,,,C0730607,,,,,Severe chronic obstructive pulmonary disease | Severe chronic obstructive pulmonary disease (disorder)
+BMGC_DS07109,BMG_DS027588,,"Hypophosphatemic Rickets, X-Linked Dominant",Familial Hypophosphatemic Rickets,,,,DOID:0050445,X-linked dominant hypophosphatemic rickets,C0733682,D053098,307800,MONDO:0010619,X-linked dominant hypophosphatemic rickets,
+BMGC_DS07110,BMG_DS027589,,,,,,,DOID:2599,glottis carcinoma,C0740083,,,MONDO:0002355,glottis carcinoma,
+BMGC_DS07111,BMG_DS027591,,,,,,,DOID:4897,bile duct carcinoma,C0740277,,,MONDO:0005496,bile duct carcinoma,
+BMGC_DS07112,BMG_DS027592,,,,,,,,,C0740302,,153550,MONDO:0007925,myelodysplastic syndrome associated with isolated del(5q),
+BMGC_DS07113,BMG_DS027593,,"Amyloidosis, Familial","Amyloidosis, Familial",,,,,,C0740340,D028226,,MONDO:0018634,hereditary amyloidosis,
+BMGC_DS07114,BMG_DS027595,,Mononeuropathy Multiplex,Mononeuropathies,,,,,,C0740343,D020422,,,,
+BMGC_DS07115,BMG_DS027596,,,,,,,DOID:903,gastrointestinal lymphoma,C0740372,,,MONDO:0004699,gastrointestinal lymphoma,
+BMGC_DS07116,BMG_DS027598,,Middle Cerebral Artery Thrombosis,"Infarction, Middle Cerebral Artery",,,,,,C0740376,D020244,,,,
+BMGC_DS07117,BMG_DS027599,,"Aneurysm, Anterior Communicating Artery",Intracranial Aneurysm,,,,,,C0740386,D002532,,,,
+BMGC_DS07118,BMG_DS027600,,"Infarction, Middle Cerebral Artery","Infarction, Middle Cerebral Artery",,,,DOID:3525,middle cerebral artery infarction,C0740392,D020244,,MONDO:0006857,middle cerebral artery infarction,
+BMGC_DS07119,BMG_DS027601,35885006;237857006;144021008;166733000;271198001,Hyperuricemia,Hyperuricemia,,,,DOID:1920,hyperuricemia,C0740394,D033461,MTHU004766,MONDO:0002144,obsolete hyperuricemia,Hyperuricemia | Uricacidemia | Hyperuricaemia | Uricacidaemia | Hyperuricemia (disorder) | Hyperuricemia | Hyperuricaemia | Hyperuricaemia (disorder) | Serum uric acid level | Blood urate | Urate - blood | (Blood urate (& serum level)) or (hyperuricemia) | (Blood urate (& serum level)) or (hyperuricaemia) | Hyperuricemia | Hyperuricaemia | (Blood urate (& serum level)) or (hyperuricaemia) (procedure) | Hyperuricaemia | Hyperuricemia | Blood urate raised | (Blood urate raized) or (hyperuricemia) | (Blood urate raised) or (hyperuricaemia) | (Blood urate raised) or (hyperuricaemia) (finding) | Hyperuricaemia | (Blood urate (& serum level)) or (hyperuricaemia) | Hyperuricemia | Blood urate | Serum uric acid level | Urate - blood | (Blood urate (& serum level)) or (hyperuricemia) | (Blood urate (& serum level)) or (hyperuricaemia) (procedure)
+BMGC_DS07120,BMG_DS027605,409966000,Acute diarrhea,,,,,,,C0740441,,,MONDO:0000257,acute diarrhea,Acute diarrhea (disorder) | Acute diarrhoea | Acute diarrhea
+BMGC_DS07121,BMG_DS027606,424736006,Diabetic peripheral neuropathy,,,,,,,C0740447,,,,,Diabetic peripheral neuropathy | Peripheral neuropathy due to diabetes mellitus (disorder) | Peripheral neuropathy due to diabetes mellitus
+BMGC_DS07122,BMG_DS027608,,,,,,,DOID:263,kidney cancer,C0740457,,,MONDO:0002367,kidney cancer,
+BMGC_DS07123,BMG_DS027609,,,,,,,DOID:3352,malignant fibrous histiocytoma of bone,C0740479,,,MONDO:0002618,undifferentiated high grade pleomorphic sarcoma of bone,
+BMGC_DS07124,BMG_DS027610,,,,,,,DOID:4848,cerebellar astrocytoma,C0740480,,,MONDO:0003165,cerebellar astrocytoma,
+BMGC_DS07125,BMG_DS027611,,,,,,,DOID:1357,maxillary sinus cancer,C0740487,,,MONDO:0001748,maxillary sinus carcinoma,
+BMGC_DS07126,BMG_DS027616,,,,,,,,,C0740858,,,MONDO:0002491,substance abuse,
+BMGC_DS07127,BMG_DS027628,,"Aortic Aneurysm, Ruptured",Aortic Rupture,,,,DOID:3627,aortic aneurysm,C0741160,D001019,,,,
+BMGC_DS07128,BMG_DS027638,,Recurrent bronchitis,,,,,,,C0741796,,MTHU011349,,,
+BMGC_DS07129,BMG_DS027641,,Cardiac Events,Cardiovascular Diseases,,,,,,C0741923,D002318,,,,
+BMGC_DS07130,BMG_DS027644,,Cerebellar vermis atrophy,,,,,,,C0742028,,MTHU009393,,,
+BMGC_DS07131,BMG_DS027646,,,,,,,DOID:3431,cerebritis,C0742115,,,MONDO:0002645,cerebritis,
+BMGC_DS07132,BMG_DS027647,,"Radiculopathy, Cervical",Radiculopathy,,,,,,C0742186,D011843,,,,
+BMGC_DS07133,BMG_DS027650,,Acute Chest Syndrome,Acute Chest Syndrome,,,,DOID:1584,acute chest syndrome,C0742343,D056586,,MONDO:0005632,acute chest syndrome,
+BMGC_DS07134,BMG_DS027658,,Conus Medullaris Syndrome,Spinal Cord Compression,,,,,,C0742803,D013117,,,,
+BMGC_DS07135,BMG_DS027659,424551004,Bacterial cystitis,,,,,,,C0742964,,,,,Bacterial cystitis (disorder) | Bacterial cystitis | Bladder infection due to Bacteria
+BMGC_DS07136,BMG_DS027662,,Granulomatous dermatitis,,,,,DOID:4397,granulomatous dermatitis,C0743086,,MTHU026378,MONDO:0006555,granulomatous dermatitis,
+BMGC_DS07137,BMG_DS027666,,Focal Dystonia,Dystonic Disorders,,,,,,C0743332,D020821,,MONDO:0000477,focal dystonia,
+BMGC_DS07138,BMG_DS027675,,,,,,,DOID:5280,gastric leiomyosarcoma,C0744295,,,MONDO:0003367,gastric leiomyosarcoma,
+BMGC_DS07139,BMG_DS027677,123752003,Immune-complex glomerulonephritis,,,,,DOID:4784,immune-complex glomerulonephritis,C0744421,,,MONDO:0003140,immune-complex glomerulonephritis,Immune-complex glomerulonephritis | Immune-complex glomerulonephritis (disorder) | Immune complex glomerulonephritis
+BMGC_DS07140,BMG_DS027689,716771000,Chronic hiccup,,,,,,,C0744898,,,MONDO:0018334,chronic hiccup,Chronic hiccup (disorder) | Chronic hiccup | Chronic hiccough | Chronic hiccups | Chronic hiccoughs
+BMGC_DS07141,BMG_DS027690,,,,,,,DOID:10159,osteonecrosis,C0745048,,,,,
+BMGC_DS07142,BMG_DS027691,,Hypereosinophilia,Eosinophilia,,,,,,C0745091,D004802,MTHU010702,,,
+BMGC_DS07143,BMG_DS027692,,Hyperlipoproteinemia Type IIa,Hyperlipoproteinemia Type II,,,,,,C0745103,D006938,143890,MONDO:0007750,"hypercholesterolemia, familial, 1",
+BMGC_DS07144,BMG_DS027693,,Isolated Systolic Hypertension,Isolated Systolic Hypertension,,,,,,C0745133,D000092244,,,,
+BMGC_DS07145,BMG_DS027694,132721000119104,Hypertensive emergency,,,,I16.1,,,C0745136,,,,,Hypertensive emergency | Hypertensive emergency (disorder)
+BMGC_DS07146,BMG_DS027695,,Hypertensive Urgency,Hypertensive Crisis,,,,,,C0745138,D000096003,,MONDO:1030007,hypertensive urgency,
+BMGC_DS07147,BMG_DS027704,,End Stage Liver Disease,End Stage Liver Disease,,,,,,C0745744,D058625,,,,
+BMGC_DS07148,BMG_DS027708,413839001,Chronic lung disease,,,,,,,C0746102,,MTHU014136,,,Chronic lung disease (disorder) | Chronic lung disease
+BMGC_DS07149,BMG_DS027714,,"Myelitis, Necrotizing","Myelitis, Transverse",,,,,,C0746706,D009188,,,,
+BMGC_DS07150,BMG_DS027715,,,,,,,DOID:5846,septal myocardial infarction,C0746727,,,MONDO:0003671,septal myocardial infarction,
+BMGC_DS07151,BMG_DS027721,,Febrile Neutropenia,Febrile Neutropenia,,,,,,C0746883,D064147,,,,
+BMGC_DS07152,BMG_DS027726,,Recurrent otitis media,,,,,,,C0747085,,MTHU001507,,,
+BMGC_DS07153,BMG_DS027727,111550004,Ovarian failure,,,,,,,C0747102,,MTHU074236,,,Ovarian failure | Ovarian failure (disorder)
+BMGC_DS07154,BMG_DS027730,,,,,,,DOID:9036,parotid gland cancer,C0747273,,,MONDO:0004700,parotid gland cancer,
+BMGC_DS07155,BMG_DS027732,,Peroneal Neuropathies,Peroneal Neuropathies,,,,DOID:4201,peroneal neuropathy,C0747533,D020427,,MONDO:0002910,peroneal neuropathy,
+BMGC_DS07156,BMG_DS027747,200977004;56210000,Erythrodermic psoriasis,,,,,,,C0748052,,MTHU068351,,,Erythrodermic psoriasis | Erythrodermic psoriasis (disorder) | Exfoliative psoriasis | Exfoliative dermatitis due to psoriasis | Psoriasis vulgaris | Erythrodermic psoriasis | Exfoliative psoriasis | Psoriasis vulgaris (disorder) | Exfoliative dermatitis due to psoriasis
+BMGC_DS07157,BMG_DS027749,,Radial Neuropathy,Radial Neuropathy,,,,DOID:12171,radial neuropathy,C0748226,D020425,,MONDO:0001459,radial neuropathy,
+BMGC_DS07158,BMG_DS027754,715401008,Reynolds syndrome,,,,,,,C0748397,,613471,MONDO:0013276,Reynolds syndrome,Primary biliary cirrhosis co-occurrent with systemic scleroderma (disorder) | Primary biliary cirrhosis co-occurrent with systemic scleroderma | Reynolds syndrome
+BMGC_DS07159,BMG_DS027755,,"HEMOLYTIC DISEASE OF FETUS AND NEWBORN, RH-INDUCED",,,,,,,C0748400,,619462,MONDO:0859172,"hemolytic disease of fetus and newborn, RH-induced",
+BMGC_DS07160,BMG_DS027758,,"Arthritis, Sacroiliac",,,,,,,C0748473,C563037,108100,MONDO:0007156,"arthritis, sacroiliac",
+BMGC_DS07161,BMG_DS027759,,"Scleroderma, Limited","Scleroderma, Limited",,,,DOID:1577,limited scleroderma,C0748540,D045745,,MONDO:0016358,limited cutaneous systemic sclerosis,
+BMGC_DS07162,BMG_DS027761,,,,,,,DOID:3643,sella turcica neoplasm,C0748616,,,MONDO:0002720,sella turcica neoplasm,
+BMGC_DS07163,BMG_DS027770,,Submandibular abscess,,DA01.30,Cellulitis or abscess of soft tissues of the mouth,K12.2,DOID:0060310,uvulitis,C0749101,,,,,
+BMGC_DS07164,BMG_DS027772,,,,,,,DOID:7587,supraglottis squamous cell carcinoma,C0749163,,,MONDO:0004293,supraglottis squamous cell carcinoma,
+BMGC_DS07165,BMG_DS027777,,,,,,,,,C0749420,,,MONDO:0019855,athyreosis,
+BMGC_DS07166,BMG_DS027778,,,,,,,DOID:8161,oncocytic carcinoma of the thyroid,C0749424,,607464,MONDO:0011836,thyroid Hurthle cell carcinoma,
+BMGC_DS07167,BMG_DS027790,,,,,,,,,C0750384,,122700,MONDO:0007390,coumarin resistance,
+BMGC_DS07168,BMG_DS027794,,Cochlear Neuritis,Vestibulocochlear Nerve Diseases,,,,,,C0750884,D000160,,,,
+BMGC_DS07169,BMG_DS027795,,Cochlear Nerve Diseases,Vestibulocochlear Nerve Diseases,,,,,,C0750885,D000160,,,,
+BMGC_DS07170,BMG_DS027796,,Vestibular Nerve Diseases,Vestibulocochlear Nerve Diseases,,,,,,C0750886,D000160,,,,
+BMGC_DS07171,BMG_DS027797,,,,,,,DOID:3953,adrenal gland cancer,C0750887,,,MONDO:0002817,adrenal gland cancer,
+BMGC_DS07172,BMG_DS027798,,"Autonomic Hyperactivity, Alcohol Withdrawal Associated",Alcohol Withdrawal Delirium,,,,,,C0750897,D000430,,,,
+BMGC_DS07173,BMG_DS027799,,"Alzheimer Disease, Early Onset",Alzheimer Disease,,,,,,C0750901,D000544,,,,
+BMGC_DS07174,BMG_DS027800,,"Amblyopia, Developmental",Amblyopia,,,,,,C0750902,D000550,,,,
+BMGC_DS07175,BMG_DS027801,,"Amblyopia, Suppression",Amblyopia,,,,DOID:10375,strabismic amblyopia,C0750903,D000550,,MONDO:0001019,suppression amblyopia,
+BMGC_DS07176,BMG_DS027802,,"Amino Acid Metabolism, Inherited Disorders","Amino Acid Metabolism, Inborn Errors",,,,,,C0750905,D000592,,,,
+BMGC_DS07177,BMG_DS027803,,,,,,,,,C0750927,,602081,MONDO:0011184,childhood apraxia of speech,
+BMGC_DS07178,BMG_DS027804,,,,,,,,,C0750929,,118420,MONDO:0007316,Chiari malformation type I,
+BMGC_DS07179,BMG_DS027807,,,,,,,DOID:3069,malignant astrocytoma,C0750935,,,MONDO:0021633,cerebral astrocytoma,
+BMGC_DS07180,BMG_DS027808,,"Tremor, Rubral",Ataxia,,,,,,C0750940,D001259,,,,
+BMGC_DS07181,BMG_DS027810,,Peripheral Autonomic Nervous System Diseases,Autonomic Nervous System Diseases,,,,,,C0750944,D001342,,,,
+BMGC_DS07182,BMG_DS027811,,"Nervous System Diseases, Parasympathetic",Autonomic Nervous System Diseases,,,,,,C0750945,D001342,,MONDO:0044995,parasympathetic nervous system disorder,
+BMGC_DS07183,BMG_DS027812,,"Nervous System Diseases, Sympathetic",Autonomic Nervous System Diseases,,,,,,C0750946,D001342,,MONDO:0044993,sympathetic nervous system disorder,
+BMGC_DS07184,BMG_DS027813,,Vertebrogenic Pain Syndrome,Back Pain,,,,,,C0750949,D001416,,,,
+BMGC_DS07185,BMG_DS027814,,Lenticulostriate Disorders,Basal Ganglia Diseases,,,,,,C0750951,D001480,,,,
+BMGC_DS07186,BMG_DS027815,,,,,,,DOID:4607,biliary tract cancer,C0750952,,,MONDO:0003060,biliary tract cancer,
+BMGC_DS07187,BMG_DS027816,,Urinary Bladder Neurogenesis,"Urinary Bladder, Neurogenic",,,,,,C0750953,D001750,,MONDO:0001445,obsolete neurogenic bladder,
+BMGC_DS07188,BMG_DS027817,,"Neurogenic Urinary Bladder, Spastic","Urinary Bladder, Neurogenic",,,,,,C0750955,D001750,,MONDO:0001445,obsolete neurogenic bladder,
+BMGC_DS07189,BMG_DS027818,,"Blindness, Monocular",Blindness,,,,,,C0750958,D001766,,,,
+BMGC_DS07190,BMG_DS027823,,Central Nervous System Metabolic Disorders,"Brain Diseases, Metabolic",,,,,,C0750968,D001928,,,,
+BMGC_DS07191,BMG_DS027824,,,,,,,DOID:1319,brain cancer,C0750974,,,MONDO:0021632,primary brain neoplasm,
+BMGC_DS07192,BMG_DS027825,,,,,,,DOID:1319,brain cancer,C0750979,,,,,
+BMGC_DS07193,BMG_DS027826,,Internal Carotid Artery Diseases,Carotid Artery Diseases,,,,,,C0750986,D002340,,,,
+BMGC_DS07194,BMG_DS027827,,"Arterial Diseases, Common Carotid",Carotid Artery Diseases,,,,,,C0750987,D002340,,,,
+BMGC_DS07195,BMG_DS027828,,Common Carotid Artery Thrombosis,Carotid Artery Thrombosis,,,,,,C0750988,D002341,,,,
+BMGC_DS07196,BMG_DS027829,,External Carotid Artery Thrombosis,Carotid Artery Thrombosis,,,,,,C0750989,D002341,,,,
+BMGC_DS07197,BMG_DS027830,,Internal Carotid Artery Thrombosis,Carotid Artery Thrombosis,,,,,,C0750990,D002341,,,,
+BMGC_DS07198,BMG_DS027832,,"Catatonia, Malignant",Catatonia,,,,,,C0750992,D002389,,,,
+BMGC_DS07199,BMG_DS027834,,"Aneurysm, Basilar Artery",Intracranial Aneurysm,,,,,,C0751001,D002532,,,,
+BMGC_DS07200,BMG_DS027835,,Brain Aneurysm,Intracranial Aneurysm,,,,,,C0751003,D002532,,MONDO:0005291,brain aneurysm,
+BMGC_DS07201,BMG_DS027836,,Giant Intracranial Aneurysm,Intracranial Aneurysm,,,,,,C0751004,D002532,,,,
+BMGC_DS07202,BMG_DS027837,,"Mycotic Aneurysm, Intracranial",Intracranial Aneurysm,,,,,,C0751005,D002532,,,,
+BMGC_DS07203,BMG_DS027838,,Intracranial Atherosclerosis,Intracranial Arteriosclerosis,,,,,,C0751007,D002537,,,,
+BMGC_DS07204,BMG_DS027839,,"Cerebral Infarction, Left Hemisphere",Cerebral Infarction,,,,,,C0751010,D002544,,,,
+BMGC_DS07205,BMG_DS027840,,"Cerebral Infarction, Right Hemisphere",Cerebral Infarction,,,,,,C0751011,D002544,,,,
+BMGC_DS07206,BMG_DS027841,,Anterior Choroidal Artery Infarction,Cerebral Infarction,,,,,,C0751012,D002544,,,,
+BMGC_DS07207,BMG_DS027842,,Subcortical Infarction,Cerebral Infarction,,,,,,C0751014,D002544,,,,
+BMGC_DS07208,BMG_DS027843,,Carotid Circulation Transient Ischemic Attack,"Ischemic Attack, Transient",,,,,,C0751019,D002546,,,,
+BMGC_DS07209,BMG_DS027844,,"Transient Ischemic Attack, Vertebrobasilar Circulation","Ischemic Attack, Transient",,,,,,C0751020,D002546,,,,
+BMGC_DS07210,BMG_DS027845,,Crescendo Transient Ischemic Attacks,"Ischemic Attack, Transient",,,,,,C0751021,D002546,,,,
+BMGC_DS07211,BMG_DS027846,,"Brain Stem Ischemia, Transient","Ischemic Attack, Transient",,,,,,C0751022,D002546,,,,
+BMGC_DS07212,BMG_DS027847,,"Cerebral Palsy, Mixed",Cerebral Palsy,,,,,,C0751024,D002547,,MONDO:0000400,mixed cerebral palsy,
+BMGC_DS07213,BMG_DS027848,,"Cerebral Palsy, Rolandic Type",Cerebral Palsy,,,,,,C0751025,D002547,,,,
+BMGC_DS07214,BMG_DS027852,,,,,,,,,C0751036,,,MONDO:0019011,Charcot-Marie-Tooth disease type 1,
+BMGC_DS07215,BMG_DS027853,,"Cockayne Syndrome, Type III",Cockayne Syndrome,,,,,,C0751037,D003057,216411,MONDO:0008998,Cockayne syndrome type 3,
+BMGC_DS07216,BMG_DS027854,,"Cockayne Syndrome, Type II",Cockayne Syndrome,,,,,,C0751038,D003057,133540,MONDO:0019570,Cockayne syndrome type 2,
+BMGC_DS07217,BMG_DS027855,,"Cockayne Syndrome, Type I",Cockayne Syndrome,,,,,,C0751039,D003057,216400,MONDO:0019569,Cockayne syndrome type 1,
+BMGC_DS07218,BMG_DS027856,,"Color Blindness, Inherited",Color Vision Defects,,,,,,C0751042,D003117,,,,
+BMGC_DS07219,BMG_DS027857,,Monochromatopsia,Color Vision Defects,,,,,,C0751043,D003117,,,,
+BMGC_DS07220,BMG_DS027858,,"Seizure, Febrile, Complex","Seizures, Febrile",,,,,,C0751057,D003294,,,,
+BMGC_DS07221,BMG_DS027859,,"Cranial Neuropathies, Multiple",Cranial Nerve Diseases,,,,,,C0751059,D003389,,,,
+BMGC_DS07222,BMG_DS027860,,"Deafness, Acquired",Deafness,,,,,,C0751068,D003638,,,,
+BMGC_DS07223,BMG_DS027861,,Diabetic Neuralgia,Diabetic Neuropathies,,,,,,C0751074,D003929,,,,
+BMGC_DS07224,BMG_DS027863,,"Diplopia, Vertical",Diplopia,,,,,,C0751079,D004172,,,,
+BMGC_DS07225,BMG_DS027864,,"Trisomy 21, Mitotic Nondisjunction",Down Syndrome,,,,,,C0751081,D004314,,,,
+BMGC_DS07226,BMG_DS027865,,"Duane Retraction Syndrome, Type 2",Duane Retraction Syndrome,,,,,,C0751083,D004370,604356,MONDO:0011444,Duane retraction syndrome 2,
+BMGC_DS07227,BMG_DS027866,,"Duane Retraction Syndrome, Type 3",Duane Retraction Syndrome,,,,,,C0751084,D004370,,,,
+BMGC_DS07228,BMG_DS027867,,"Dyskinesia, Medication-Induced","Dyskinesia, Drug-Induced",,,,,,C0751088,D004409,,,,
+BMGC_DS07229,BMG_DS027868,,,,,,,DOID:5101,ear cancer,C0751094,,,,,
+BMGC_DS07230,BMG_DS027869,,"Empty Sella Syndrome, Secondary",Empty Sella Syndrome,,,,,,C0751097,D004652,,,,
+BMGC_DS07231,BMG_DS027871,,"Encephalomyelitis, Postexanthem","Encephalomyelitis, Acute Disseminated",,,,,,C0751099,D004673,,,,
+BMGC_DS07232,BMG_DS027872,,Postinfectious Encephalomyelitis,"Encephalomyelitis, Acute Disseminated",,,,,,C0751100,D004673,,,,
+BMGC_DS07233,BMG_DS027873,,Post-Vaccinal Encephalitis,"Encephalomyelitis, Acute Disseminated",,,,DOID:13664,post-vaccinal encephalitis,C0751101,D004673,,MONDO:0001773,post-vaccinal encephalitis,
+BMGC_DS07234,BMG_DS027878,,"Leukoencephalitis, Subacute Hemorrhagic","Leukoencephalitis, Acute Hemorrhagic",,,,,,C0751108,D004684,,,,
+BMGC_DS07235,BMG_DS027879,,Single Seizure,Seizures,,,,,,C0751110,D012640,,,,
+BMGC_DS07236,BMG_DS027880,,Awakening Epilepsy,Epilepsy,,,,,,C0751111,D004827,,,,
+BMGC_DS07237,BMG_DS027881,,Subclinical Seizure,"Epilepsies, Partial",,,,,,C0751112,D004828,,,,
+BMGC_DS07238,BMG_DS027882,,Uncinate Seizures,"Epilepsies, Partial",,,,,,C0751113,D004828,,,,
+BMGC_DS07239,BMG_DS027883,,Digestive Epilepsy,"Epilepsies, Partial",,,,,,C0751115,D004828,,,,
+BMGC_DS07240,BMG_DS027884,,Cryptogenic Tonic-Clonic Epilepsy,"Epilepsy, Tonic-Clonic",,,,,,C0751117,D004830,,,,
+BMGC_DS07241,BMG_DS027885,,"Epilepsy, Tonic-Clonic, Familial","Epilepsy, Tonic-Clonic",,,,,,C0751118,D004830,,,,
+BMGC_DS07242,BMG_DS027886,,"Epilepsy, Tonic-Clonic, Symptomatic","Epilepsy, Tonic-Clonic",,,,,,C0751119,D004830,,,,
+BMGC_DS07243,BMG_DS027887,,Benign Infantile Myoclonic Epilepsy,"Epilepsies, Myoclonic",,,,,,C0751120,D004831,,MONDO:0100566,myoclonic epilepsy in infancy,
+BMGC_DS07244,BMG_DS027888,,Infantile Severe Myoclonic Epilepsy,"Epilepsies, Myoclonic",,,,,,C0751122,D004831,,MONDO:0100135,Dravet syndrome,
+BMGC_DS07245,BMG_DS027889,,Atonic Absence Seizures,Seizures,,,,,,C0751123,D012640,,,,
+BMGC_DS07246,BMG_DS027890,,"Epilepsy, Absence, Atypical","Epilepsy, Absence",,,,DOID:0070309,absence epilepsy,C0751124,D004832,,,,
+BMGC_DS07247,BMG_DS027892,,Facial Neuritis,Facial Nerve Diseases,,,,,,C0751131,D005155,,,,
+BMGC_DS07248,BMG_DS027893,,Familial Facial Neuropathy,Facial Nerve Diseases,,,,,,C0751132,D005155,,,,
+BMGC_DS07249,BMG_DS027894,,Acquired Facial Neuropathy,Facial Nerve Diseases,,,,,,C0751133,D005155,,,,
+BMGC_DS07250,BMG_DS027896,,"Fibromyalgia, Primary",Fibromyalgia,,,,,,C0751152,D005356,,,,
+BMGC_DS07251,BMG_DS027897,,"Fibromyalgia, Secondary",Fibromyalgia,,,,,,C0751153,D005356,,,,
+BMGC_DS07252,BMG_DS027898,,FRAXA Syndrome,Fragile X Syndrome,,,,,,C0751156,D005600,,,,
+BMGC_DS07253,BMG_DS027899,,FRAXE Syndrome,Fragile X Syndrome,,,,,,C0751157,D005600,309548,MONDO:0010659,FRAXE intellectual disability,
+BMGC_DS07254,BMG_DS027900,,,,,,,DOID:0111458,galactose epimerase deficiency,C0751161,,230350,MONDO:0009257,galactose epimerase deficiency,
+BMGC_DS07255,BMG_DS027902,,Adult Glycogen Storage Disease Type II,Glycogen Storage Disease Type II,,,,,,C0751172,D006009,,,,
+BMGC_DS07256,BMG_DS027903,,"Glycogen Storage Disease Type II, Infantile",Glycogen Storage Disease Type II,,,,,,C0751173,D006009,,,,
+BMGC_DS07257,BMG_DS027904,,"Glycogen Storage Disease Type II, Juvenile",Glycogen Storage Disease Type II,,,,,,C0751174,D006009,,,,
+BMGC_DS07258,BMG_DS027905,,Primary Cough Headache,"Headache Disorders, Primary",,,,,,C0751185,D051270,,,,
+BMGC_DS07259,BMG_DS027906,,Fulminant Hepatic Failure with Cerebral Edema,Hepatic Encephalopathy,,,,,,C0751197,D006501,,,,
+BMGC_DS07260,BMG_DS027907,,Hepatic Stupor,Hepatic Encephalopathy,,,,,,C0751198,D006501,,,,
+BMGC_DS07261,BMG_DS027908,,Cystathionine beta-Synthase Deficiency Disease,Homocystinuria,,,,,,C0751202,D006712,236200,MONDO:0009352,classic homocystinuria,
+BMGC_DS07262,BMG_DS027913,,Akinetic-Rigid Variant of Huntington Disease,Huntington Disease,,,,,,C0751207,D006816,,,,
+BMGC_DS07263,BMG_DS027914,,Juvenile Huntington Disease,Huntington Disease,,,,,,C0751208,D006816,,MONDO:0016621,juvenile Huntington disease,
+BMGC_DS07264,BMG_DS027915,,Inappropriate ACTH Secretion Syndrome,Pituitary ACTH Hypersecretion,,,,,,C0751220,D047748,,,,
+BMGC_DS07265,BMG_DS027919,,"Hypersomnia, Recurrent",Disorders of Excessive Somnolence,,,,DOID:8619,recurrent hypersomnia,C0751226,D006970,,MONDO:0004617,recurrent hypersomnia,
+BMGC_DS07266,BMG_DS027920,,"Hypersomnolence Disorders, Primary",Disorders of Excessive Somnolence,,,,,,C0751227,D006970,,,,
+BMGC_DS07267,BMG_DS027921,,"Hypersomnolence Disorders, Secondary",Disorders of Excessive Somnolence,,,,,,C0751228,D006970,,,,
+BMGC_DS07268,BMG_DS027922,,Hypothalamic Dysfunction Syndromes,Hypothalamic Diseases,,,,,,C0751230,D007027,,MONDO:0043101,hypothalamic dysfunction,
+BMGC_DS07269,BMG_DS027923,,Hypothalamic Dysinhibition Syndrome,Hypothalamic Diseases,,,,,,C0751231,D007027,,,,
+BMGC_DS07270,BMG_DS027924,,Hypothalamic Overactivity Syndrome,Hypothalamic Diseases,,,,,,C0751232,D007027,,,,
+BMGC_DS07271,BMG_DS027925,,Hypothalamic-Adenohypophyseal Disorders,Hypothalamic Diseases,,,,,,C0751233,D007027,,,,
+BMGC_DS07272,BMG_DS027926,,Hypothalamic-Neurohypophyseal Disorders,Hypothalamic Diseases,,,,,,C0751234,D007027,,,,
+BMGC_DS07273,BMG_DS027927,,Pituitary Diencephalic Syndrome,Hypothalamic Diseases,,,,,,C0751235,D007027,,,,
+BMGC_DS07274,BMG_DS027928,,Chronic Insomnia,Sleep Initiation and Maintenance Disorders,,,,,,C0751249,D007319,,,,
+BMGC_DS07275,BMG_DS027929,,Psychophysiological Insomnia,Sleep Initiation and Maintenance Disorders,,,,,,C0751250,D007319,,,,
+BMGC_DS07276,BMG_DS027930,,Sleep Initiation Dysfunction,Sleep Initiation and Maintenance Disorders,,,,,,C0751252,D007319,,,,
+BMGC_DS07277,BMG_DS027931,,"Creutzfeldt-Jakob Disease, Familial",Creutzfeldt-Jakob Syndrome,,,,,,C0751254,D007562,123400,MONDO:0007403,inherited Creutzfeldt-Jakob disease,
+BMGC_DS07278,BMG_DS027933,,"Auditory Processing Disorder, Central",Language Development Disorders,,,,,,C0751257,D007805,,MONDO:0024422,auditory perceptual disorders,
+BMGC_DS07279,BMG_DS027934,,,,,,,DOID:8927,learning disability,C0751265,,,MONDO:0004681,learning disability,
+BMGC_DS07280,BMG_DS027935,,"Encephalopathy, Subacute Necrotizing, Infantile",Leigh Disease,,,,,,C0751267,D007888,,,,
+BMGC_DS07281,BMG_DS027936,,"Encephalopathy, Subacute Necrotizing, Juvenile",Leigh Disease,,,,,,C0751268,D007888,,,,
+BMGC_DS07282,BMG_DS027937,,Infantile Globoid Cell Leukodystrophy,"Leukodystrophy, Globoid Cell",,,,,,C0751273,D007965,,MONDO:0016089,infantile Krabbe disease,
+BMGC_DS07283,BMG_DS027938,44359008,"Metachromatic leukodystrophy, juvenile type",,,,,,,C0751276,,250100,MONDO:0009591,"metachromatic leukodystrophy, juvenile form","Metachromatic leukodystrophy, juvenile type | Metachromatic leucodystrophy, juvenile type | Scholz-Bielschowsky-Henneberg diffuse cerebral sclerosis | Juvenile metachromatic leucodystrophy | Scholz cerebral sclerosis | Metachromatic leukodystrophy, juvenile type (disorder)"
+BMGC_DS07284,BMG_DS027939,,"Metachromatic Leukodystrophy, Infant","Leukodystrophy, Metachromatic",,,,,,C0751278,D007966,,MONDO:0017729,"metachromatic leukodystrophy, late infantile form",
+BMGC_DS07285,BMG_DS027940,,"Leukodystrophy, Metachromatic, Adult","Leukodystrophy, Metachromatic",,,,,,C0751279,D007966,,MONDO:0017730,"metachromatic leukodystrophy, adult form",
+BMGC_DS07286,BMG_DS027942,,"Maple Syrup Urine Disease, Thiamine Responsive",Maple Syrup Urine Disease,,,,,,C0751285,D008375,,MONDO:0017054,thiamine-responsive maple syrup urine disease,
+BMGC_DS07287,BMG_DS027943,,,,,,,,,C0751291,,,MONDO:0016711,desmoplastic/nodular medulloblastoma,
+BMGC_DS07288,BMG_DS027944,,,,,,,DOID:6114,cerebral convexity meningioma,C0751303,,,MONDO:0003774,cerebral convexity meningioma,
+BMGC_DS07289,BMG_DS027945,,,,,,,DOID:6869,parasagittal meningioma,C0751304,,,MONDO:0004022,parasagittal meningioma,
+BMGC_DS07290,BMG_DS027946,,"Meningitis, Haemophilus parainfluenzae","Meningitis, Haemophilus",,,,DOID:0080179,haemophilus meningitis,C0751307,D008583,,,,
+BMGC_DS07291,BMG_DS027947,,"Meningitis, Haemophilus influenzae Type F","Meningitis, Haemophilus",,,,DOID:0080179,haemophilus meningitis,C0751308,D008583,,,,
+BMGC_DS07292,BMG_DS027948,,"Meningitis, Pneumococcal, Penicillin-Resistant","Meningitis, Pneumococcal",,,,,,C0751313,D008586,,,,
+BMGC_DS07293,BMG_DS027949,,,,,,,DOID:0060326,myelomeningocele,C0751316,,,,,
+BMGC_DS07294,BMG_DS027950,,"Moyamoya Disease, Primary",Moyamoya Disease,,,,,,C0751322,D009072,,,,
+BMGC_DS07295,BMG_DS027951,,"Moyamoya Disease, Secondary",Moyamoya Disease,,,,,,C0751323,D009072,,,,
+BMGC_DS07296,BMG_DS027952,,"Multiple Sclerosis, Acute Fulminating",Multiple Sclerosis,,,,,,C0751324,D009103,,,,
+BMGC_DS07297,BMG_DS027953,,Progressive Proximal Myelopathic Muscular Atrophy,"Muscular Atrophy, Spinal",,,,,,C0751334,D009134,,,,
+BMGC_DS07298,BMG_DS027954,,Scapuloperoneal Form of Spinal Muscular Atrophy,"Muscular Atrophy, Spinal",,,,DOID:0111552,scapuloperoneal spinal muscular atrophy,C0751335,D009134,181405,MONDO:0008408,"scapuloperoneal spinal muscular atrophy, autosomal dominant",
+BMGC_DS07299,BMG_DS027955,,Distal Muscular Dystrophies,Distal Myopathies,,,,DOID:11720,distal myopathy,C0751336,D049310,,MONDO:0018949,distal myopathy,
+BMGC_DS07300,BMG_DS027956,,X-Linked Emery-Dreifuss Muscular Dystrophy,X-Linked Emery-Dreifuss Muscular Dystrophy,,,,,,C0751337,D000083143,,MONDO:0010680,X-linked Emery-Dreifuss muscular dystrophy,
+BMGC_DS07301,BMG_DS027957,,"Myasthenia Gravis, Generalized",Myasthenia Gravis,,,,,,C0751339,D009157,,,,
+BMGC_DS07302,BMG_DS027958,,"Myasthenia Gravis, Ocular",Myasthenia Gravis,,,,,,C0751340,D009157,,,,
+BMGC_DS07303,BMG_DS027960,,"Myelitis, Paraneoplastic","Myelitis, Transverse",,,,,,C0751342,D009188,,,,
+BMGC_DS07304,BMG_DS027961,,"Myelitis, Postinfectious","Myelitis, Transverse",,,,,,C0751343,D009188,,,,
+BMGC_DS07305,BMG_DS027962,,"Myelitis, Postvaccinal","Myelitis, Transverse",,,,,,C0751344,D009188,,,,
+BMGC_DS07306,BMG_DS027963,,"Myelitis, Subacute Transverse","Myelitis, Transverse",,,,,,C0751345,D009188,,,,
+BMGC_DS07307,BMG_DS027964,,Demyelinative Myelitis,"Myelitis, Transverse",,,,,,C0751346,D009188,,,,
+BMGC_DS07308,BMG_DS027965,,"Myoclonus, Eyelid",Myoclonus,,,,,,C0751349,D009207,,,,
+BMGC_DS07309,BMG_DS027966,,Idiopathic Inflammatory Myopathies,Myositis,,,,,,C0751356,D009220,,MONDO:0600023,idiopathic inflammatory myopathy,
+BMGC_DS07310,BMG_DS027967,,"Myositis, Focal",Myositis,,,,,,C0751357,D009220,,,,
+BMGC_DS07311,BMG_DS027968,,Becker Generalized Myotonia,Myotonia Congenita,,,,,,C0751360,D009224,255700,MONDO:0009715;MONDO:0009710,"Thomsen and Becker disease | myotonia congenita, autosomal recessive",
+BMGC_DS07312,BMG_DS027969,,Narcolepsy-Cataplexy Syndrome,Narcolepsy,,,,,,C0751362,D009290,,MONDO:0016158,narcolepsy-cataplexy syndrome,
+BMGC_DS07313,BMG_DS027970,,External Nerve Compression Syndromes,Nerve Compression Syndromes,,,,,,C0751367,D009408,,,,
+BMGC_DS07314,BMG_DS027971,,Internal Nerve Compression Syndromes,Nerve Compression Syndromes,,,,,,C0751368,D009408,,,,
+BMGC_DS07315,BMG_DS027972,,Neuroleptic-Induced Neuroleptic Malignant Syndrome,Neuroleptic Malignant Syndrome,,,,,,C0751376,D009459,,,,
+BMGC_DS07316,BMG_DS027973,,Foley-Denny-Brown Syndrome,Neuromuscular Diseases,,,,,,C0751381,D009468,,MONDO:0035586,Cramp-fasciculation syndrome,
+BMGC_DS07317,BMG_DS027974,,Juvenile Neuronal Ceroid Lipofuscinosis,Neuronal Ceroid-Lipofuscinoses,,,,,,C0751383,D009472,204200,MONDO:0008767,neuronal ceroid lipofuscinosis 3,
+BMGC_DS07318,BMG_DS027975,,,,,,,DOID:3181,oligodendroglioma,C0751396,,,,,
+BMGC_DS07319,BMG_DS027979,,Optic Disk Disorders,Optic Nerve Diseases,,,,,,C0751402,D009901,,,,
+BMGC_DS07320,BMG_DS027980,,Post-Traumatic Osteoporosis,Osteoporosis,,,,,,C0751406,D010024,,,,
+BMGC_DS07321,BMG_DS027982,,"Parkinson Disease, Secondary Vascular","Parkinson Disease, Secondary",,,,,,C0751414,D010302,,,,
+BMGC_DS07322,BMG_DS027983,,Atherosclerotic Parkinsonism,"Parkinson Disease, Secondary",,,,,,C0751415,D010302,,,,
+BMGC_DS07323,BMG_DS027984,,Hereditary Autoinflammatory Diseases,Hereditary Autoinflammatory Diseases,,,,,,C0751422,D056660,,MONDO:0017953,hereditary periodic fever syndrome,
+BMGC_DS07324,BMG_DS027987,7573000,Classical phenylketonuria,,5C50.00,Classical phenylketonuria,E70.0,,,C0751434,,,MONDO:0019259,classic phenylketonuria,"Classical phenylketonuria | Imbecilitus phenylpyruvica | Hyperphenylalaninemia, type I | Severe phenylalanine hydroxylase deficiency | Hyperphenylalaninaemia, type I | Classical phenylketonuria (disorder)"
+BMGC_DS07325,BMG_DS027988,68528007,Hyperphenylalaninaemia,Phenylketonurias,,,,,,C0751435,D010661,,,,Hyperphenylalaninemia | Hyperphenylalaninaemia | Hyperphenylalaninemia (disorder)
+BMGC_DS07326,BMG_DS027989,,"Hyperphenylalaninemia, Non-Phenylketonuric",Phenylketonurias,,,,,,C0751436,D010661,,MONDO:0016543,hyperphenylalaninemia due to tetrahydrobiopterin deficiency,
+BMGC_DS07327,BMG_DS027990,,Adenohypophyseal Diseases,Pituitary Diseases,,,,,,C0751437,D010900,,MONDO:0024468,anterior pituitary gland disorder,
+BMGC_DS07328,BMG_DS027994,,"Encephalitis, Polio",Poliomyelitis,,,,,,C0751445,D011051,,,,
+BMGC_DS07329,BMG_DS027995,,"Poliomyelitis, Nonpoliovirus",Poliomyelitis,,,,,,C0751446,D011051,,,,
+BMGC_DS07330,BMG_DS027996,,"Poliomyelitis, Preparalytic",Poliomyelitis,,,,,,C0751447,D011051,,,,
+BMGC_DS07331,BMG_DS027997,,"Polyneuropathy, Familial",Polyneuropathies,,,,,,C0751448,D011115,,,,
+BMGC_DS07332,BMG_DS027998,,Acquired Polyneuropathy,Polyneuropathies,,,,,,C0751449,D011115,,,,
+BMGC_DS07333,BMG_DS028000,,Flaccid Quadriplegia,Quadriplegia,,,,,,C0751460,D011782,,,,
+BMGC_DS07334,BMG_DS028001,,"Paralysis, Spinal, Quadriplegic",Quadriplegia,,,,,,C0751461,D011782,,,,
+BMGC_DS07335,BMG_DS028002,,Nerve Root Compression,Radiculopathy,,,,,,C0751463,D011843,,,,
+BMGC_DS07336,BMG_DS028003,,,,,,,DOID:4648,familial retinoblastoma,C0751483,,180200,MONDO:0018160,hereditary retinoblastoma,
+BMGC_DS07337,BMG_DS028004,,"Reye Syndrome, Adult",Reye Syndrome,,,,,,C0751485,D012202,,,,
+BMGC_DS07338,BMG_DS028005,,Reye-Like Syndrome,Reye Syndrome,,,,,,C0751486,D012202,,,,
+BMGC_DS07339,BMG_DS028006,,Adult Sandhoff Disease,Sandhoff Disease,,,,,,C0751489,D012497,,MONDO:0017723,"Sandhoff disease, adult form",
+BMGC_DS07340,BMG_DS028007,,Infantile Sandhoff Disease,Sandhoff Disease,,,,,,C0751490,D012497,,MONDO:0017721,"Sandhoff disease, infantile form",
+BMGC_DS07341,BMG_DS028008,,Juvenile Sandhoff Disease,Sandhoff Disease,,,,,,C0751491,D012497,,MONDO:0017722,"Sandhoff disease, juvenile form",
+BMGC_DS07342,BMG_DS028009,,"Seizures, Focal",Seizures,,,,,,C0751495,D012640,,,,
+BMGC_DS07343,BMG_DS028010,,Special Senses Disorders,Sensation Disorders,,,,,,C0751497,D012678,,,,
+BMGC_DS07344,BMG_DS028011,,Petrous Sinus Thrombophlebitis,"Sinus Thrombosis, Intracranial",,,,,,C0751500,D012851,,,,
+BMGC_DS07345,BMG_DS028012,,Intracranial Sinus Thrombophlebitis,"Sinus Thrombosis, Intracranial",,,,,,C0751501,D012851,,,,
+BMGC_DS07346,BMG_DS028013,,Petrous Sinus Thrombosis,"Sinus Thrombosis, Intracranial",,,,,,C0751502,D012851,,,,
+BMGC_DS07347,BMG_DS028014,,Insufficient Sleep Syndrome,Sleep Deprivation,,,,,,C0751505,D012892,,,,
+BMGC_DS07348,BMG_DS028015,,REM Sleep Deprivation,Sleep Deprivation,,,,,,C0751506,D012892,,,,
+BMGC_DS07349,BMG_DS028016,,Sleep-Related Neurogenic Tachypnea,Sleep Wake Disorders,,,,,,C0751510,D012893,,MONDO:0019045,obsolete rare sleep disorder,
+BMGC_DS07350,BMG_DS028017,,Verbal Fluency Disorders,Speech Disorders,,,,,,C0751514,D013064,,,,
+BMGC_DS07351,BMG_DS028018,,"Status Epilepticus, Subclinical",Status Epilepticus,,,,,,C0751522,D013226,,,,
+BMGC_DS07352,BMG_DS028019,,Non-Convulsive Status Epilepticus,Status Epilepticus,,,,,,C0751523,D013226,,,,
+BMGC_DS07353,BMG_DS028020,,Simple Partial Status Epilepticus,Status Epilepticus,,,,,,C0751524,D013226,,,,
+BMGC_DS07354,BMG_DS028021,,Convergent Comitant Strabismus,Strabismus,,,,,,C0751525,D013285,,,,
+BMGC_DS07355,BMG_DS028022,,"Strabismus, Noncomitant",Strabismus,,,,,,C0751526,D013285,,,,
+BMGC_DS07356,BMG_DS028023,,,,,,,DOID:0060243,stuttering,C0751527,,,,,
+BMGC_DS07357,BMG_DS028024,,,,,,,DOID:0060243,stuttering,C0751528,,,,,
+BMGC_DS07358,BMG_DS028025,,,,,,,DOID:0060243,stuttering,C0751529,,,,,
+BMGC_DS07359,BMG_DS028029,,"Syncope, Deglutitional",Syncope,,,,,,C0751537,D013575,,,,
+BMGC_DS07360,BMG_DS028030,,"Syncope, Hyperventilation",Syncope,,,,,,C0751538,D013575,,,,
+BMGC_DS07361,BMG_DS028031,,"Syncope, Stokes-Adams",Syncope,,,,,,C0751539,D013575,,,,
+BMGC_DS07362,BMG_DS028034,,Tangier Disease Neuropathy,Tangier Disease,,,,,,C0751544,D013631,,,,
+BMGC_DS07363,BMG_DS028035,,Giant Cell Aortic Arteritis,Giant Cell Arteritis,,,,,,C0751545,D013700,,,,
+BMGC_DS07364,BMG_DS028036,,Juvenile Temporal Arteritis,Giant Cell Arteritis,,,,,,C0751547,D013700,,MONDO:0016848,juvenile temporal arteritis,
+BMGC_DS07365,BMG_DS028040,,,,,,,DOID:3277,thymus cancer,C0751552,,,MONDO:0002586,thymus cancer,
+BMGC_DS07366,BMG_DS028041,,Childhood Tic Disorders,Tic Disorders,,,,,,C0751553,D013981,,,,
+BMGC_DS07367,BMG_DS028042,,Motor Tic Disorders,Tic Disorders,,,,,,C0751554,D013981,,,,
+BMGC_DS07368,BMG_DS028043,,Pulsatile Tinnitus,Tinnitus,,,,,,C0751559,D014012,,,,
+BMGC_DS07369,BMG_DS028044,,,,,,,DOID:8858,tonsil cancer,C0751560,,,MONDO:0006998,tonsil cancer,
+BMGC_DS07370,BMG_DS028047,,Vertebrobasilar Dolichoectasia,Vertebrobasilar Insufficiency,,,,,,C0751572,D014715,,,,
+BMGC_DS07371,BMG_DS028051,,"Encephalitis, West Nile Fever",West Nile Fever,,,,DOID:2365,West Nile encephalitis,C0751583,D014901,,MONDO:0019376,West-Nile encephalitis,
+BMGC_DS07372,BMG_DS028052,,West Nile Fever Meningitis,West Nile Fever,,,,,,C0751584,D014901,,,,
+BMGC_DS07373,BMG_DS028053,,West Nile Fever Meningoencephalitis,West Nile Fever,,,,,,C0751585,D014901,,,,
+BMGC_DS07374,BMG_DS028054,,West Nile Fever Myelitis,West Nile Fever,,,,,,C0751586,D014901,,,,
+BMGC_DS07375,BMG_DS028055,,,,,,,DOID:13945,CADASIL,C0751587,,,MONDO:0007432,cerebral arteriopathy with subcortical infarcts and leukoencephalopathy,
+BMGC_DS07376,BMG_DS028056,,,,,,,DOID:1659,supratentorial cancer,C0751589,,,MONDO:0002071,supratentorial cancer,
+BMGC_DS07377,BMG_DS028057,,,,,,,DOID:4706,infratentorial cancer,C0751593,,,MONDO:0003107,infratentorial cancer,
+BMGC_DS07378,BMG_DS028058,,Zellweger-Like Syndrome,Zellweger Syndrome,,,,,,C0751594,D015211,,,,
+BMGC_DS07379,BMG_DS028059,,Juvenile Pyruvate Dehydrogenase Complex Deficiency Disease,Pyruvate Dehydrogenase Complex Deficiency Disease,,,,,,C0751595,D015325,,,,
+BMGC_DS07380,BMG_DS028060,,"Pyruvate Dehydrogenase Complex Deficiency Disease, Neonatal",Pyruvate Dehydrogenase Complex Deficiency Disease,,,,,,C0751596,D015325,,,,
+BMGC_DS07381,BMG_DS028061,,"Ataxia with Lactic Acidosis, Type I",Pyruvate Dehydrogenase Complex Deficiency Disease,,,,,,C0751597,D015325,,,,
+BMGC_DS07382,BMG_DS028062,,Hereditary Autosomal Dominant Spastic Paraplegia,"Spastic Paraplegia, Hereditary",,,,,,C0751602,D015419,,,,
+BMGC_DS07383,BMG_DS028063,,Autosomal Recessive Hereditary Spastic Paraplegia,"Spastic Paraplegia, Hereditary",,,,,,C0751603,D015419,,,,
+BMGC_DS07384,BMG_DS028064,,Hereditary X-Linked Recessive Spastic Paraplegia,"Spastic Paraplegia, Hereditary",,,,,,C0751604,D015419,,,,
+BMGC_DS07385,BMG_DS028065,,"X-Linked, Spastic Paraplegia, Hereditary","Spastic Paraplegia, Hereditary",,,,,,C0751605,D015419,,,,
+BMGC_DS07386,BMG_DS028066,,,,,,,DOID:5604,adult acute lymphocytic leukemia,C0751606,,,MONDO:0003541,adult acute lymphoblastic leukemia,
+BMGC_DS07387,BMG_DS028068,,"Eosinophilia-Myalgia Syndrome, L-Tryptophan-Related",Eosinophilia-Myalgia Syndrome,,,,,,C0751622,D016603,,,,
+BMGC_DS07388,BMG_DS028070,,"Toxoplasmosis, Central Nervous System","Toxoplasmosis, Cerebral",,,,,,C0751629,D016781,,,,
+BMGC_DS07389,BMG_DS028071,,Intracranial Toxoplasmosis,"Toxoplasmosis, Cerebral",,,,,,C0751630,D016781,,,,
+BMGC_DS07390,BMG_DS028072,,Neurotoxoplasmosis,"Toxoplasmosis, Cerebral",,,,,,C0751631,D016781,,,,
+BMGC_DS07391,BMG_DS028073,,Common Carotid Artery Stenosis,Carotid Stenosis,,,,,,C0751635,D016893,,,,
+BMGC_DS07392,BMG_DS028074,,External Carotid Artery Stenosis,Carotid Stenosis,,,,,,C0751636,D016893,,,,
+BMGC_DS07393,BMG_DS028075,,Granulomous Cerebral Cryptococcosis,"Meningitis, Cryptococcal",,,,DOID:0080159,Cryptococcal meningitis,C0751637,D016919,,,,
+BMGC_DS07394,BMG_DS028077,,Cryptogenic Partial Complex Epilepsy,"Epilepsy, Complex Partial",,,,,,C0751640,D017029,,,,
+BMGC_DS07395,BMG_DS028078,,"Epilepsy, Symptomatic, Partial Complex","Epilepsy, Complex Partial",,,,,,C0751641,D017029,,,,
+BMGC_DS07396,BMG_DS028079,,"Epilepsy, Anterior Fronto-Polar","Epilepsy, Frontal Lobe",,,,,,C0751642,D017034,,,,
+BMGC_DS07397,BMG_DS028080,,"Epilepsy, Orbito-Frontal","Epilepsy, Frontal Lobe",,,,,,C0751643,D017034,,,,
+BMGC_DS07398,BMG_DS028081,,"Human Transmissible Spongiform Encephalopathies, Inherited",Prion Diseases,,,,,,C0751645,D017096,,,,
+BMGC_DS07399,BMG_DS028082,,Pseudoakathisia,"Akathisia, Drug-Induced",,,,,,C0751647,D017109,,,,
+BMGC_DS07400,BMG_DS028083,,Mitochondrial Diseases,Mitochondrial Diseases,,,,DOID:700,mitochondrial metabolism disease,C0751651,D028361,,MONDO:0044970,mitochondrial disease,
+BMGC_DS07401,BMG_DS028088,,"Amyloid Neuropathy, Secondary",Amyloid Neuropathies,,,,,,C0751660,D017772,,,,
+BMGC_DS07402,BMG_DS028089,,"Canavan Disease, Familial Form",Canavan Disease,,,,,,C0751663,D017825,,,,
+BMGC_DS07403,BMG_DS028090,,"Canavan Disease, Neonatal",Canavan Disease,,,,,,C0751664,D017825,,,,
+BMGC_DS07404,BMG_DS028091,,"Canavan Disease, Sporadic Form",Canavan Disease,,,,,,C0751665,D017825,,,,
+BMGC_DS07405,BMG_DS028092,,"Canavan Disease, Infantile",Canavan Disease,,,,,,C0751666,D017825,,,,
+BMGC_DS07406,BMG_DS028093,,"Canavan Disease, Juvenile",Canavan Disease,,,,,,C0751667,D017825,,,,
+BMGC_DS07407,BMG_DS028094,,Machado-Joseph Disease Type I,Machado-Joseph Disease,,,,,,C0751668,D017827,,MONDO:0017174,Machado-Joseph disease type 1,
+BMGC_DS07408,BMG_DS028095,,Machado-Joseph Disease Type II,Machado-Joseph Disease,,,,,,C0751669,D017827,,MONDO:0017175,Machado-Joseph disease type 2,
+BMGC_DS07409,BMG_DS028096,,Machado-Joseph Disease Type III,Machado-Joseph Disease,,,,,,C0751670,D017827,,MONDO:0017176,Machado-Joseph disease type 3,
+BMGC_DS07410,BMG_DS028097,,Machado-Joseph Disease Type IV,Machado-Joseph Disease,,,,,,C0751671,D017827,,,,
+BMGC_DS07411,BMG_DS028098,,,,,,,,,C0751674,,606690,MONDO:0011705,lymphangioleiomyomatosis,
+BMGC_DS07412,BMG_DS028099,,,,,,,DOID:7398,cerebral primitive neuroectodermal tumor,C0751675,,,MONDO:0004209,cerebral primitive neuroectodermal tumor,
+BMGC_DS07413,BMG_DS028100,,,,,,,DOID:1749,squamous cell carcinoma,C0751688,,,,,
+BMGC_DS07414,BMG_DS028101,,,,,,,DOID:3193,peripheral nerve sheath neoplasm,C0751689,,,,,
+BMGC_DS07415,BMG_DS028102,,,,,,,DOID:5940,malignant peripheral nerve sheath tumor,C0751690,,,MONDO:0017827,malignant peripheral nerve sheath tumor,
+BMGC_DS07416,BMG_DS028103,,,,,,,DOID:4697,perineurioma,C0751691,,,MONDO:0019404,perineurioma,
+BMGC_DS07417,BMG_DS028104,,Brown-Sequard's Paralysis,Brown-Sequard Syndrome,,,,,,C0751693,D018437,,,,
+BMGC_DS07418,BMG_DS028105,,Spastic Spinal Monoplegia Syndrome,Brown-Sequard Syndrome,,,,,,C0751694,D018437,,,,
+BMGC_DS07419,BMG_DS028112,,Tension-Vascular Headache,Tension-Type Headache,,,,,,C0751705,D018781,,,,
+BMGC_DS07420,BMG_DS028113,,,,,,,,,C0751706,,,MONDO:0015059,progressive non-fluent aphasia,
+BMGC_DS07421,BMG_DS028114,,"Peroxisomal Dysfunction, General",Peroxisomal Disorders,,,,,,C0751708,D018901,,,,
+BMGC_DS07422,BMG_DS028115,,"Peroxisomal Dysfunction, Multiple",Peroxisomal Disorders,,,,,,C0751709,D018901,,,,
+BMGC_DS07423,BMG_DS028116,,"Peroxisomal Dysfunction, Single",Peroxisomal Disorders,,,,,,C0751710,D018901,,,,
+BMGC_DS07424,BMG_DS028117,,Anterior Ischemic Optic Neuropathy,"Optic Neuropathy, Ischemic",,,,,,C0751711,D018917,,MONDO:0006649,anterior ischemic optic neuropathy,
+BMGC_DS07425,BMG_DS028118,,Posterior Ischemic Optic Neuropathy,"Optic Neuropathy, Ischemic",,,,,,C0751712,D018917,,,,
+BMGC_DS07426,BMG_DS028119,,"Inclusion Body Myopathy, Sporadic","Myositis, Inclusion Body",,,,,,C0751713,D018979,,,,
+BMGC_DS07427,BMG_DS028120,,Adult Neuroaxonal Dystrophy,Neuroaxonal Dystrophies,,,,,,C0751716,D019150,,,,
+BMGC_DS07428,BMG_DS028121,,Juvenile Neuroaxonal Dystrophy,Neuroaxonal Dystrophies,,,,,,C0751717,D019150,,,,
+BMGC_DS07429,BMG_DS028122,,Late Infantile Neuroaxonal Dystrophy,Neuroaxonal Dystrophies,,,,,,C0751718,D019150,,,,
+BMGC_DS07430,BMG_DS028126,,"Blindness, Cortical, Post-Ictal","Blindness, Cortical",,,,,,C0751729,D019575,,,,
+BMGC_DS07431,BMG_DS028127,,Anton Syndrome,"Blindness, Cortical",,,,,,C0751730,D019575,,,,
+BMGC_DS07432,BMG_DS028130,,"Degenerative Diseases, Spinal Cord",Neurodegenerative Diseases,,,,,,C0751733,D019636,,,,
+BMGC_DS07433,BMG_DS028132,,Basal Ganglia Cerebrovascular Disease,Basal Ganglia Cerebrovascular Disease,,,,DOID:10991,basal ganglia cerebrovascular disease,C0751739,D020144,,MONDO:0006505,basal ganglia cerebrovascular disorder,
+BMGC_DS07434,BMG_DS028133,,Lenticulostriate Vasculopathy,Basal Ganglia Cerebrovascular Disease,,,,,,C0751740,D020144,,,,
+BMGC_DS07435,BMG_DS028134,,"Metabolic Disorder, Central Nervous System, Acquired","Brain Diseases, Metabolic",,,,,,C0751743,D001928,,,,
+BMGC_DS07436,BMG_DS028135,,"Brain Diseases, Metabolic, Acquired","Brain Diseases, Metabolic",,,,,,C0751744,D001928,,,,
+BMGC_DS07437,BMG_DS028137,,"Hyperglycinemia, Nonketotic, Type III","Hyperglycinemia, Nonketotic",,,,,,C0751747,D020158,,,,
+BMGC_DS07438,BMG_DS028138,,Nonketotic Hyperglycinemia,"Hyperglycinemia, Nonketotic",,,,DOID:9268,glycine encephalopathy,C0751748,D020158,,MONDO:0011612,glycine encephalopathy,
+BMGC_DS07439,BMG_DS028139,,"Argininosuccinic Acid Synthetase Deficiency Disease, Partial",Citrullinemia,,,,,,C0751750,D020159,,,,
+BMGC_DS07440,BMG_DS028140,,"Argininosuccinic Acid Synthetase Deficiency, Complete",Citrullinemia,,,,,,C0751751,D020159,,,,
+BMGC_DS07441,BMG_DS028141,,Carbamoyl-Phosphate Synthase I Deficiency Disease,Carbamoyl-Phosphate Synthase I Deficiency Disease,,,,DOID:9280,carbamoyl phosphate synthetase I deficiency disease,C0751753,D020165,,,,
+BMGC_DS07442,BMG_DS028143,,Advanced Sleep Phase Syndrome,"Sleep Disorders, Circadian Rhythm",,,,,,C0751758,D020178,,MONDO:0024378,"circadian rhythm sleep disorder, advanced sleep phase type",
+BMGC_DS07443,BMG_DS028145,,Upper Airway Resistance Sleep Apnea Syndrome,"Sleep Apnea, Obstructive",,,,,,C0751761,D020181,,,,
+BMGC_DS07444,BMG_DS028146,,"Central Sleep Apnea, Primary","Sleep Apnea, Central",,,,,,C0751762,D020182,,MONDO:0024356,primary central sleep apnea syndrome,
+BMGC_DS07445,BMG_DS028147,,"Central Sleep Apnea, Secondary","Sleep Apnea, Central",,,,,,C0751763,D020182,,,,
+BMGC_DS07446,BMG_DS028151,,,,,,,DOID:9091,REM sleep behavior disorder,C0751772,,,MONDO:0005937,REM sleep behavior disorder,
+BMGC_DS07447,BMG_DS028152,,Nocturnal Myoclonus Syndrome,Nocturnal Myoclonus Syndrome,,,,DOID:9207,periodic limb movement disorder,C0751774,D020189,,MONDO:0005905,periodic limb movement disorder,
+BMGC_DS07448,BMG_DS028153,,Atypical Inclusion-Body Disease,"Myoclonic Epilepsies, Progressive",,,,,,C0751776,D020191,,,,
+BMGC_DS07449,BMG_DS028154,,Familial Progressive Myoclonic Epilepsy,"Myoclonic Epilepsies, Progressive",,,,,,C0751777,D020191,,,,
+BMGC_DS07450,BMG_DS028155,,"Myoclonic Epilepsies, Progressive","Myoclonic Epilepsies, Progressive",,,,DOID:891,progressive myoclonus epilepsy,C0751778,D020191,,MONDO:0020074,progressive myoclonus epilepsy,
+BMGC_DS07451,BMG_DS028156,,Action Myoclonus-Renal Failure Syndrome,"Myoclonic Epilepsies, Progressive",,,,DOID:0111444,progressive myoclonus epilepsy 4,C0751779,D020191,254900,MONDO:0009699,action myoclonus-renal failure syndrome,
+BMGC_DS07452,BMG_DS028157,,Biotin-Responsive Encephalopathy,"Myoclonic Epilepsies, Progressive",,,,,,C0751780,D020191,,,,
+BMGC_DS07453,BMG_DS028158,,Dentatorubral-Pallidoluysian Atrophy,"Myoclonic Epilepsies, Progressive",,,,DOID:0060162,dentatorubral-pallidoluysian atrophy,C0751781,D020191,125370,MONDO:0007435,dentatorubral-pallidoluysian atrophy,
+BMGC_DS07454,BMG_DS028159,,May-White Syndrome,"Myoclonic Epilepsies, Progressive",,,,,,C0751782,D020191,,,,
+BMGC_DS07455,BMG_DS028160,,Lafora Disease,Lafora Disease,,,,DOID:3534,Lafora disease,C0751783,D020192,,MONDO:0009697,Lafora disease,
+BMGC_DS07456,BMG_DS028161,,"Lafora Body Disease, Late Onset",Lafora Disease,,,,,,C0751784,D020192,,,,
+BMGC_DS07457,BMG_DS028162,,Unverricht-Lundborg Syndrome,Unverricht-Lundborg Syndrome,,,,DOID:3535,Unverricht-Lundborg syndrome,C0751785,D020194,254800,MONDO:0009698,Unverricht-Lundborg syndrome,
+BMGC_DS07458,BMG_DS028163,,Decision Making Reflex Epilepsy,"Epilepsy, Reflex",,,,,,C0751786,D020195,,,,
+BMGC_DS07459,BMG_DS028164,,"Reflex Epilepsy, Eating-Induced","Epilepsy, Reflex",,,,,,C0751787,D020195,,,,
+BMGC_DS07460,BMG_DS028165,,"Reflex Epilepsy, Visual Pattern","Epilepsy, Reflex",,,,,,C0751788,D020195,,,,
+BMGC_DS07461,BMG_DS028166,,Tactile Reflex Epilepsy,"Epilepsy, Reflex",,,,,,C0751789,D020195,,,,
+BMGC_DS07462,BMG_DS028167,,Writing-Induced Reflex Epilepsy,"Epilepsy, Reflex",,,,,,C0751790,D020195,,,,
+BMGC_DS07463,BMG_DS028168,,"Reflex Epilepsy, Audiogenic","Epilepsy, Reflex",,,,,,C0751791,D020195,,MONDO:0015644,audiogenic seizures,
+BMGC_DS07464,BMG_DS028169,,"Coma, Post-Traumatic, Prolonged","Coma, Post-Head Injury",,,,,,C0751812,D020207,,,,
+BMGC_DS07465,BMG_DS028170,,"Carotid Artery, Internal, Dissection","Carotid Artery, Internal, Dissection",,,,,,C0751815,D020215,,,,
+BMGC_DS07466,BMG_DS028173,,"Septic Phlebitis, Sagittal Sinus",Sagittal Sinus Thrombosis,,,,,,C0751823,D020225,,,,
+BMGC_DS07467,BMG_DS028174,,Sagittal Sinus Thrombophlebitis,Sagittal Sinus Thrombosis,,,,,,C0751824,D020225,,,,
+BMGC_DS07468,BMG_DS028175,,"Septic Phlebitis, Cavernous Sinus",Cavernous Sinus Thrombosis,,,,,,C0751825,D020226,,,,
+BMGC_DS07469,BMG_DS028178,,"Gait Disorder, Sensorimotor","Gait Disorders, Neurologic",,,,,,C0751829,D020233,,,,
+BMGC_DS07470,BMG_DS028179,,"Gait Disorders, Neurologic","Gait Disorders, Neurologic",,,,,,C0751830,D020233,,,,
+BMGC_DS07471,BMG_DS028183,,"Infarction, Anterior Cerebral Artery","Infarction, Anterior Cerebral Artery",,,,DOID:3528,anterior cerebral artery infarction,C0751843,D020243,,MONDO:0006647,anterior cerebral artery infarction,
+BMGC_DS07472,BMG_DS028185,,Middle Cerebral Artery Embolus,"Infarction, Middle Cerebral Artery",,,,,,C0751845,D020244,,,,
+BMGC_DS07473,BMG_DS028186,,Left Middle Cerebral Artery Infarction,"Infarction, Middle Cerebral Artery",,,,,,C0751846,D020244,,,,
+BMGC_DS07474,BMG_DS028187,,"Embolic Infarction, Middle Cerebral Artery","Infarction, Middle Cerebral Artery",,,,,,C0751847,D020244,,,,
+BMGC_DS07475,BMG_DS028188,,"Thrombotic Infarction, Middle Cerebral Artery","Infarction, Middle Cerebral Artery",,,,,,C0751848,D020244,,,,
+BMGC_DS07476,BMG_DS028189,,Right Middle Cerebral Artery Infarction,"Infarction, Middle Cerebral Artery",,,,,,C0751849,D020244,,,,
+BMGC_DS07477,BMG_DS028190,,Arsenic Encephalopathy,Arsenic Poisoning,,,,,,C0751851,D020261,,,,
+BMGC_DS07478,BMG_DS028191,,Mercurial Neuroanesthenia,"Mercury Poisoning, Nervous System",,,,,,C0751857,D020262,,,,
+BMGC_DS07479,BMG_DS028192,,"Lead Encephalopathy, Childhood","Lead Poisoning, Nervous System, Childhood",,,,,,C0751860,D020264,,,,
+BMGC_DS07480,BMG_DS028193,,Lead Polyneuropathy,"Lead Poisoning, Nervous System, Adult",,,,,,C0751862,D020265,,,,
+BMGC_DS07481,BMG_DS028194,,MPTP-Induced Degeneration of the Striatum,MPTP Poisoning,,,,,,C0751864,D020267,,,,
+BMGC_DS07482,BMG_DS028195,,"Alcohol-Induced Disorders, Nervous System","Alcohol-Induced Disorders, Nervous System",,,,,,C0751865,D020268,,,,
+BMGC_DS07483,BMG_DS028197,,Alcohol Withdrawal-Induced Major Motor Seizure,Alcohol Withdrawal Seizures,,,,,,C0751868,D020270,,,,
+BMGC_DS07484,BMG_DS028198,,"Status Epilepticus, Alcohol Withdrawal-Induced",Alcohol Withdrawal Seizures,,,,,,C0751869,D020270,,,,
+BMGC_DS07485,BMG_DS028199,,"Heredodegenerative Disorders, Nervous System","Heredodegenerative Disorders, Nervous System",,,,,,C0751870,D020271,,,,
+BMGC_DS07486,BMG_DS028200,,Autoimmune Diseases of the Nervous System,Autoimmune Diseases of the Nervous System,,,,DOID:438,autoimmune disease of the nervous system,C0751871,D020274,,MONDO:0002977,autoimmune disorder of the nervous system,
+BMGC_DS07487,BMG_DS028201,,"Immune Disorders, Nervous System",Autoimmune Diseases of the Nervous System,,,,,,C0751872,D020274,,,,
+BMGC_DS07488,BMG_DS028206,,"Vasculitis, Central Nervous System","Vasculitis, Central Nervous System",,,,DOID:525,central nervous system vasculitis,C0751878,D020293,,MONDO:0003346,central nervous system vasculitis,
+BMGC_DS07489,BMG_DS028207,,Secondary CNS Vasculitis,"Vasculitis, Central Nervous System",,,,,,C0751879,D020293,,,,
+BMGC_DS07490,BMG_DS028208,,Postzoster Arteritis,"Vasculitis, Central Nervous System",,,,,,C0751880,D020293,,,,
+BMGC_DS07491,BMG_DS028209,,Primary CNS Vasculitis,"Vasculitis, Central Nervous System",,,,,,C0751881,D020293,,,,
+BMGC_DS07492,BMG_DS028210,,"Myasthenic Syndromes, Congenital","Myasthenic Syndromes, Congenital",,,,DOID:3635,congenital myasthenic syndrome,C0751882,D020294,,MONDO:0018940,congenital myasthenic syndrome,
+BMGC_DS07493,BMG_DS028211,,"Congenital Myasthenic Syndromes, Postsynaptic","Myasthenic Syndromes, Congenital",,,,,,C0751883,D020294,,MONDO:0020344,postsynaptic congenital myasthenic syndrome,
+BMGC_DS07494,BMG_DS028212,,"Congenital Myasthenic Syndromes, Presynaptic","Myasthenic Syndromes, Congenital",,,,,,C0751884,D020294,,,,
+BMGC_DS07495,BMG_DS028213,,"Myasthenic Syndromes, Congenital, Slow Channel","Myasthenic Syndromes, Congenital",,,,,,C0751885,D020294,,,,
+BMGC_DS07496,BMG_DS028214,,,,,,,DOID:4203,brain stem cancer,C0751886,,,,,
+BMGC_DS07497,BMG_DS028215,,"Vasospasm, Intracranial","Vasospasm, Intracranial",,,,DOID:13100,intracranial vasospasm,C0751895,D020301,,MONDO:0006812,intracranial vasospasm,
+BMGC_DS07498,BMG_DS028216,,Migraine with Acute Onset Aura,Migraine with Aura,,,,,,C0751904,D020325,,,,
+BMGC_DS07499,BMG_DS028218,,Subacute Vestibular Neuritis,Vestibular Neuronitis,,,,,,C0751907,D020338,,,,
+BMGC_DS07500,BMG_DS028219,,Vestibular Neuronitis,Vestibular Neuronitis,,,,DOID:12683,vestibular neuronitis,C0751908,D020338,,MONDO:0006008,vestibular neuronitis,
+BMGC_DS07501,BMG_DS028220,,Vestibular Neuropathy,Vestibular Neuronitis,,,,,,C0751909,D020338,,,,
+BMGC_DS07502,BMG_DS028224,,Adult Pelizaeus-Merzbacher Disease,Pelizaeus-Merzbacher Disease,,,,,,C0751914,D020371,,,,
+BMGC_DS07503,BMG_DS028225,,"Pelizaeus-Merzbacher Disease, Atypical",Pelizaeus-Merzbacher Disease,,,,,,C0751915,D020371,,,,
+BMGC_DS07504,BMG_DS028226,,Classic Pelizaeus-Merzbacher Disease,Pelizaeus-Merzbacher Disease,,,,,,C0751916,D020371,,MONDO:0017222,"Pelizaeus-Merzbacher disease, classic form",
+BMGC_DS07505,BMG_DS028227,,"Pelizaeus-Merzbacher Disease, Transitional",Pelizaeus-Merzbacher Disease,,,,,,C0751917,D020371,,MONDO:0017223,"Pelizaeus-Merzbacher disease, transitional form",
+BMGC_DS07506,BMG_DS028228,,Cockayne-Pelizaeus-Merzbacher Disease,Pelizaeus-Merzbacher Disease,,,,,,C0751918,D020371,,,,
+BMGC_DS07507,BMG_DS028229,,Acquired Neuromyotonia,Isaacs Syndrome,,,,,,C0751919,D020386,,,,
+BMGC_DS07508,BMG_DS028230,,"Medial Neuropathy, Distal",Median Neuropathy,,,,,,C0751920,D020423,,,,
+BMGC_DS07509,BMG_DS028231,,Median Neuropathy,Median Neuropathy,,,,,,C0751922,D020423,,MONDO:0003598,median nerve neuropathy,
+BMGC_DS07510,BMG_DS028232,,"Neuralgia-Neuritis, Sciatic Nerve",Sciatic Neuropathy,,,,,,C0751924,D020426,,,,
+BMGC_DS07511,BMG_DS028233,,Sciatic Nerve Palsy,Sciatic Neuropathy,,,,,,C0751925,D020426,,,,
+BMGC_DS07512,BMG_DS028234,,"Neuropathy, Common Peroneal",Peroneal Neuropathies,,,,,,C0751926,D020427,,,,
+BMGC_DS07513,BMG_DS028235,,Fibular Neuropathy,Peroneal Neuropathies,,,,,,C0751927,D020427,,,,
+BMGC_DS07514,BMG_DS028236,,"Neuropathy, Deep Peroneal",Peroneal Neuropathies,,,,,,C0751928,D020427,,,,
+BMGC_DS07515,BMG_DS028237,,"Neuropathy, Superficial Peroneal",Peroneal Neuropathies,,,,,,C0751929,D020427,,,,
+BMGC_DS07516,BMG_DS028238,,Femoral Neuritis,Femoral Neuropathy,,,,,,C0751930,D020428,,,,
+BMGC_DS07517,BMG_DS028239,,Femoral Neuropathy,Femoral Neuropathy,,,,DOID:4196,femoral neuropathy,C0751931,D020428,,MONDO:0006759,femoral neuropathy,
+BMGC_DS07518,BMG_DS028240,,Tibial Neuropathy,Tibial Neuropathy,,,,DOID:1187,tibial neuropathy,C0751932,D020429,,MONDO:0006997,tibial neuropathy,
+BMGC_DS07519,BMG_DS028245,,,,,,,DOID:367,olfactory nerve disease,C0751937,,,MONDO:0002727,olfactory nerve disorder,
+BMGC_DS07520,BMG_DS028246,,"Superior Oblique Palsy, Neurogenic",Trochlear Nerve Diseases,,,,DOID:13864,trochlear nerve disease,C0751939,D020432,,,,
+BMGC_DS07521,BMG_DS028247,,"Abducens Palsy, Childhood, Benign Recurrent",Abducens Nerve Diseases,,,,,,C0751940,D020434,,,,
+BMGC_DS07522,BMG_DS028249,,Glossopharyngeal Motor Neuropathy,Glossopharyngeal Nerve Diseases,,,,DOID:7558,glossopharyngeal motor neuropathy,C0751942,D020435,,MONDO:0004279,glossopharyngeal motor neuropathy,
+BMGC_DS07523,BMG_DS028252,,Hypoglossal Neuropathy,Hypoglossal Nerve Diseases,,,,,,C0751945,D020437,,,,
+BMGC_DS07524,BMG_DS028253,,"Neonatal Sleep Myoclonus, Benign",Parasomnias,,,,,,C0751946,D020447,,,,
+BMGC_DS07525,BMG_DS028254,,Sleep-Related Abnormal Swallowing Syndrome,Parasomnias,,,,,,C0751948,D020447,,,,
+BMGC_DS07526,BMG_DS028255,,Neuromuscular Junction Diseases,Neuromuscular Junction Diseases,,,,DOID:439,neuromuscular junction disease,C0751950,D020511,,MONDO:0020124,neuromuscular junction disease,
+BMGC_DS07527,BMG_DS028256,,"Myopathy, Central Core","Myopathy, Central Core",,,,DOID:3529,congenital myopathy 1A,C0751951,D020512,,,,
+BMGC_DS07528,BMG_DS028257,,Anterior Circulation Brain Infarction,Brain Infarction,,,,,,C0751952,D020520,,,,
+BMGC_DS07529,BMG_DS028258,,"Brain Infarction, Posterior Circulation",Brain Infarction,,,,,,C0751953,D020520,,,,
+BMGC_DS07530,BMG_DS028259,,"Venous Infarction, Brain",Brain Infarction,,,,,,C0751954,D020520,,,,
+BMGC_DS07531,BMG_DS028260,,Brain Infarction,Brain Infarction,,,,DOID:3454,brain infarction,C0751955,D020520,,MONDO:0005394,brain infarction,
+BMGC_DS07532,BMG_DS028261,,Acute Cerebrovascular Accidents,Stroke,,,,,,C0751956,D020521,,,,
+BMGC_DS07533,BMG_DS028262,,"Lymphoma, Lymphocytic, Intermediate","Lymphoma, Mantle-Cell",,,,DOID:0050746,mantle cell lymphoma,C0751958,D020522,,,,
+BMGC_DS07534,BMG_DS028263,,Millard-Gublar Syndrome,Brain Stem Infarctions,,,,,,C0751963,D020526,,,,
+BMGC_DS07535,BMG_DS028264,,"Multiple Sclerosis, Primary Progressive","Multiple Sclerosis, Chronic Progressive",,,,DOID:0050784,primary progressive multiple sclerosis,C0751964,D020528,,MONDO:0000451,primary progressive multiple sclerosis,
+BMGC_DS07536,BMG_DS028265,,"Multiple Sclerosis, Secondary Progressive","Multiple Sclerosis, Chronic Progressive",,,,DOID:0050783,secondary progressive multiple sclerosis,C0751965,D020528,,MONDO:0000450,secondary progressive multiple sclerosis,
+BMGC_DS07537,BMG_DS028266,,"Multiple Sclerosis, Relapsing-Remitting","Multiple Sclerosis, Relapsing-Remitting",,,,DOID:2378,relapsing-remitting multiple sclerosis,C0751967,D020529,,MONDO:0005314,relapsing-remitting multiple sclerosis,
+BMGC_DS07538,BMG_DS028267,,Hypocatalasemia,Acatalasia,,,,,,C0752048,D020642,,,,
+BMGC_DS07539,BMG_DS028268,,Autosomal Dominant Juvenile Parkinson Disease,Parkinsonian Disorders,,,,,,C0752097,D020734,,,,
+BMGC_DS07540,BMG_DS028269,,Autosomal Dominant Parkinsonism,Parkinsonian Disorders,,,,,,C0752098,D020734,,,,
+BMGC_DS07541,BMG_DS028270,,Autosomal Recessive Parkinsonism,Parkinsonian Disorders,,,,,,C0752100,D020734,,,,
+BMGC_DS07542,BMG_DS028271,,Familial Juvenile Parkinsonism,Parkinsonian Disorders,,,,,,C0752104,D020734,,,,
+BMGC_DS07543,BMG_DS028272,,"Parkinsonism, Juvenile",Parkinsonian Disorders,,,,,,C0752105,D020734,,MONDO:0000828,juvenile-onset Parkinson disease,
+BMGC_DS07544,BMG_DS028273,,"Brain Diseases, Metabolic, Inherited","Brain Diseases, Metabolic, Inborn",,,,,,C0752107,D020739,,,,
+BMGC_DS07545,BMG_DS028274,,"Brain Diseases, Metabolic, Inborn","Brain Diseases, Metabolic, Inborn",,,,,,C0752109,D020739,,,,
+BMGC_DS07546,BMG_DS028275,,Central Nervous System Inborn Metabolic Diseases,"Brain Diseases, Metabolic, Inborn",,,,,,C0752110,D020739,,,,
+BMGC_DS07547,BMG_DS028276,,Spinocerebellar Ataxia Type 1,Spinocerebellar Ataxias,,,,,,C0752120,D020754,164400,MONDO:0008119,spinocerebellar ataxia type 1,
+BMGC_DS07548,BMG_DS028277,,Spinocerebellar Ataxia Type 2,Spinocerebellar Ataxias,,,,,,C0752121,D020754,183090,MONDO:0008458,spinocerebellar ataxia type 2,
+BMGC_DS07549,BMG_DS028278,,Spinocerebellar Ataxia Type 4,Spinocerebellar Ataxias,,,,DOID:0050957,spinocerebellar ataxia type 4,C0752122,D020754,600223,MONDO:0010847,spinocerebellar ataxia type 4,
+BMGC_DS07550,BMG_DS028279,,Spinocerebellar Ataxia Type 5,Spinocerebellar Ataxias,,,,,,C0752123,D020754,600224,MONDO:0010848,spinocerebellar ataxia type 5,
+BMGC_DS07551,BMG_DS028280,,,,,,,,,C0752124,,183086,MONDO:0008457,spinocerebellar ataxia type 6,
+BMGC_DS07552,BMG_DS028281,,Spinocerebellar Ataxia Type 7,Spinocerebellar Ataxias,,,,,,C0752125,D020754,164500,MONDO:0016163,autosomal dominant cerebellar ataxia type II,
+BMGC_DS07553,BMG_DS028282,,Spinal Cord Vascular Diseases,Spinal Cord Vascular Diseases,,,,DOID:178,vascular disease,C0752127,D020758,,,,
+BMGC_DS07554,BMG_DS028283,,Posterior Spinal Artery Syndrome,Spinal Cord Vascular Diseases,,,,,,C0752128,D020758,,,,
+BMGC_DS07555,BMG_DS028284,,Spinal Cord Ischemia,Spinal Cord Ischemia,,,,DOID:178,vascular disease,C0752130,D020760,,MONDO:0020688,spinal cord ischemia,
+BMGC_DS07556,BMG_DS028285,,"Infarction, Posterior Cerebral Artery","Infarction, Posterior Cerebral Artery",,,,DOID:3821,posterior cerebral artery infarction,C0752132,D020762,,MONDO:0006917,posterior cerebral artery infarction,
+BMGC_DS07557,BMG_DS028286,,"Embolic Infarction, Posterior Cerebral Artery","Infarction, Posterior Cerebral Artery",,,,,,C0752133,D020762,,,,
+BMGC_DS07558,BMG_DS028287,,"Thrombotic Infarction, Posterior Cerebral Artery","Infarction, Posterior Cerebral Artery",,,,,,C0752134,D020762,,,,
+BMGC_DS07559,BMG_DS028288,,"Brain Diseases, Arterial",Intracranial Arterial Diseases,,,,,,C0752137,D020765,,,,
+BMGC_DS07560,BMG_DS028289,,Intracranial Arterial Diseases,Intracranial Arterial Diseases,,,,DOID:13089,intracranial arterial disease,C0752138,D020765,,MONDO:0006808,intracranial arterial disease,
+BMGC_DS07561,BMG_DS028290,,Intracranial Embolism,Intracranial Embolism,,,,DOID:4372,intracranial embolism,C0752140,D020766,,MONDO:0006809,intracranial embolism,
+BMGC_DS07562,BMG_DS028291,,Intracranial Thrombosis,Intracranial Thrombosis,,,,DOID:4193,intracranial thrombosis,C0752143,D020767,,MONDO:0002907,intracranial thrombosis,
+BMGC_DS07563,BMG_DS028292,,Brain Thrombosis,Intracranial Thrombosis,,,,,,C0752144,D020767,,,,
+BMGC_DS07564,BMG_DS028294,,Chronic Daily Headache,Headache Disorders,,,,,,C0752147,D020773,,,,
+BMGC_DS07565,BMG_DS028295,,"Headache, Intractable",Headache Disorders,,,,,,C0752149,D020773,,,,
+BMGC_DS07566,BMG_DS028296,,Hypnic Headache,"Headache Disorders, Primary",,,,,,C0752150,D051270,,MONDO:0017181,hypnic headache,
+BMGC_DS07567,BMG_DS028298,,Bardet-Biedl Syndrome,Bardet-Biedl Syndrome,,,,DOID:1935,Bardet-Biedl syndrome,C0752166,D020788,,MONDO:0015229,Bardet-Biedl syndrome,
+BMGC_DS07568,BMG_DS028306,1177012000,Neuroschistosomiasis,Neuroschistosomiasis,,,,DOID:13722,neuroschistosomiasis,C0752191,D020818,,MONDO:0005874,neuroschistosomiasis,Infection of nervous system caused by Schistosoma (disorder) | Neuroschistosomiasis | Infection of nervous system caused by Schistosoma
+BMGC_DS07569,BMG_DS028311,426592006,Ballismus,Dyskinesias,,,,,,C0752196,D020820,MTHU055453,,,Ballism (disorder) | Ballismus | Ballism
+BMGC_DS07570,BMG_DS028312,,Adult-Onset Dystonias,Dystonic Disorders,,,,,,C0752197,D020821,,,,
+BMGC_DS07571,BMG_DS028313,,Adult-Onset Idiopathic Focal Dystonias,Dystonic Disorders,,,,,,C0752198,D020821,,,,
+BMGC_DS07572,BMG_DS028314,,Adult-Onset Idiopathic Torsion Dystonias,Dystonic Disorders,,,,,,C0752199,D020821,,,,
+BMGC_DS07573,BMG_DS028315,,Autosomal Dominant Familial Dystonia,Dystonic Disorders,,,,,,C0752200,D020821,,,,
+BMGC_DS07574,BMG_DS028316,,Autosomal Recessive Familial Dystonia,Dystonic Disorders,,,,,,C0752201,D020821,,,,
+BMGC_DS07575,BMG_DS028317,,Childhood Onset Dystonias,Dystonic Disorders,,,,,,C0752202,D020821,,,,
+BMGC_DS07576,BMG_DS028318,,"Dystonia, Primary",Dystonic Disorders,,,,,,C0752203,D020821,,,,
+BMGC_DS07577,BMG_DS028319,,"Dystonia, Secondary",Dystonic Disorders,,,,,,C0752205,D020821,,,,
+BMGC_DS07578,BMG_DS028320,,"Dystonias, Sporadic",Dystonic Disorders,,,,,,C0752206,D020821,,,,
+BMGC_DS07579,BMG_DS028321,,Familial Dystonia,Dystonic Disorders,,,,DOID:0050835,generalized dystonia,C0752207,D020821,,,,
+BMGC_DS07580,BMG_DS028322,,Pseudodystonia,Dystonic Disorders,,,,,,C0752208,D020821,,MONDO:0019114,psychogenic movement disorders,
+BMGC_DS07581,BMG_DS028323,,"Dyskinesias, Paroxysmal",Chorea,,,,,,C0752210,D002819,,MONDO:0015427,paroxysmal dyskinesia,
+BMGC_DS07582,BMG_DS028326,,Lyme Neuroborreliosis,Lyme Neuroborreliosis,,,,DOID:11729,Lyme disease,C0752235,D020852,,,,
+BMGC_DS07583,BMG_DS028333,,Position Sense Disorders,Somatosensory Disorders,,,,,,C0752258,D020886,,,,
+BMGC_DS07584,BMG_DS028334,,Thermal Sensation Disorders,Somatosensory Disorders,,,,,,C0752261,D020886,,,,
+BMGC_DS07585,BMG_DS028335,,Somatosensory Disorders,Somatosensory Disorders,,,,,,C0752262,D020886,,,,
+BMGC_DS07586,BMG_DS028336,,Congenital Structural Myopathy,"Myopathies, Structural, Congenital",,,,DOID:422,congenital structural myopathy,C0752282,D020914,,MONDO:0002921,congenital structural myopathy,
+BMGC_DS07587,BMG_DS028339,,Environmental Sleep Disorder,Dyssomnias,,,,,,C0752289,D020920,,,,
+BMGC_DS07588,BMG_DS028340,,"Sleep Disorders, Extrinsic",Dyssomnias,,,,,,C0752293,D020920,,,,
+BMGC_DS07589,BMG_DS028348,,Hypoxic-Ischemic Encephalopathy,"Hypoxia-Ischemia, Brain",,,,,,C0752304,D020925,,,,
+BMGC_DS07590,BMG_DS028349,,Anoxic-Ischemic Encephalopathy,"Hypoxia-Ischemia, Brain",,,,,,C0752305,D020925,,,,
+BMGC_DS07591,BMG_DS028350,,"Anoxia-Ischemia, Brain","Hypoxia-Ischemia, Brain",,,,,,C0752306,D020925,,,,
+BMGC_DS07592,BMG_DS028351,,"Anoxia-Ischemia, Cerebral","Hypoxia-Ischemia, Brain",,,,,,C0752307,D020925,,,,
+BMGC_DS07593,BMG_DS028352,,"Hypoxia-Ischemia, Brain","Hypoxia-Ischemia, Brain",,,,,,C0752308,D020925,,MONDO:0006685,brain hypoxia - ischemia,
+BMGC_DS07594,BMG_DS028353,,"Epilepsy, Partial, Sensory","Epilepsy, Partial, Sensory",,,,DOID:3330,partial sensory epilepsy,C0752322,D020937,,,,
+BMGC_DS07595,BMG_DS028354,,Focal Clonic Seizures,"Epilepsy, Partial, Motor",,,,,,C0752323,D020938,,,,
+BMGC_DS07596,BMG_DS028361,,"Lupus Vasculitis, Central Nervous System","Lupus Vasculitis, Central Nervous System",,,,,,C0752332,D020945,,MONDO:0043985,central nervous system lupus,
+BMGC_DS07597,BMG_DS028362,,Lupus Meningoencephalitis,"Lupus Vasculitis, Central Nervous System",,,,,,C0752334,D020945,,,,
+BMGC_DS07598,BMG_DS028363,,Neuropsychiatric Systemic Lupus Erythematosus,"Lupus Vasculitis, Central Nervous System",,,,,,C0752335,D020945,,,,
+BMGC_DS07599,BMG_DS028365,,Neuroaspergillosis,Neuroaspergillosis,,,,DOID:13565,neuroaspergillosis,C0752342,D020953,,MONDO:0005873,neuroaspergillosis,
+BMGC_DS07600,BMG_DS028366,,Lewy Body Disease,Lewy Body Disease,,,,DOID:12217,Lewy body dementia,C0752347,D020961,127750,MONDO:0007488,Lewy body dementia,
+BMGC_DS07601,BMG_DS028367,,"Muscular Disorders, Atrophic","Muscular Disorders, Atrophic",,,,DOID:913,atrophic muscular disease,C0752352,D020966,,MONDO:0004714,atrophic muscular disease,
+BMGC_DS07602,BMG_DS028369,,,,,,,,,C0752355,,,MONDO:0020481,myotonia fluctuans,
+BMGC_DS07603,BMG_DS028373,71444005,Cerebral arterial thrombosis,,,,,,,C0795687,,,,,Cerebral thrombosis | Thrombosis of cerebral arteries | Cerebral arterial thrombosis | Cerebral arterial thrombosis (disorder) | CT - Cerebral thrombosis
+BMGC_DS07604,BMG_DS028374,,,,,,,DOID:0060327;DOID:0060321,omphalocele | umbilical hernia,C0795690,,,MONDO:0019015,omphalocele,
+BMGC_DS07605,BMG_DS028391,718189004,Recombinant chromosome 8 syndrome,,,,,,,C0795822,C535296,179613,MONDO:0008365,recombinant 8 syndrome,Recombinant chromosome 8 syndrome (disorder) | Recombinant chromosome 8 syndrome | San Luis Valley syndrome
+BMGC_DS07606,BMG_DS028396,,CHROMOSOME 9p DELETION SYNDROME,,,,,,,C0795830,,158170,MONDO:0008013,chromosome 9p deletion syndrome,
+BMGC_DS07607,BMG_DS028398,,KLEEFSTRA SYNDROME 1,,,,,DOID:0060352,Kleefstra syndrome 1,C0795833,,607001;610253,MONDO:0027407,Kleefstra syndrome 1,
+BMGC_DS07608,BMG_DS028403,,Jacobsen Distal 11q Deletion Syndrome,Jacobsen Distal 11q Deletion Syndrome,,,,DOID:0111723,Jacobsen Syndrome,C0795841,D054868,147791,MONDO:0007838,Jacobsen syndrome,
+BMGC_DS07609,BMG_DS028416,401315004,Smith-Magenis syndrome,,,,Q93.88,,,C0795864,,182290,MONDO:0008434,Smith-Magenis syndrome,Smith-Magenis syndrome (disorder) | Smith-Magenis syndrome
+BMGC_DS07610,BMG_DS028426,,,,,,,,,C0795888,,300830,MONDO:0010440,"autism, susceptibility to, X-linked 4",
+BMGC_DS07611,BMG_DS028427,,,,,,,,,C0795889,,300523,MONDO:0010354,Allan-Herndon-Dudley syndrome,
+BMGC_DS07612,BMG_DS028429,,Alopecia contractures dwarfism mental retardation,,,,,,,C0795895,C537051,203550,MONDO:0008754,alopecia - contractures - dwarfism - intellectual disability syndrome,
+BMGC_DS07613,BMG_DS028430,,Cleft Palate-Lateral Synechia Syndrome,,,,,DOID:0080313,cleft palate-lateral synechia syndrome,C0795898,C563047,119550,MONDO:0007337,cleft palate-lateral synechia syndrome,
+BMGC_DS07614,BMG_DS028432,,"Coloboma, cleft lip-palate and mental retardation syndrome",,,,,DOID:0111249,uveal coloboma-cleft lip and palate-intellectual disability,C0795902,C535971,,,,
+BMGC_DS07615,BMG_DS028433,239087008,Cantu syndrome,,,,,DOID:0060569,hypertrichotic osteochondrodysplasia Cantu type,C0795905,C535572,239850,MONDO:0009406,hypertrichotic osteochondrodysplasia Cantu type,Cantu's syndrome | Cantu's syndrome (disorder) | Cantu syndrome
+BMGC_DS07616,BMG_DS028434,,CONOTRUNCAL ANOMALY FACE SYNDROME,,,,,,,C0795907,,217095,,,
+BMGC_DS07617,BMG_DS028435,,COWCHOCK SYNDROME,,,,,,,C0795910,,310490;300169,MONDO:0010689,Charcot-Marie-Tooth disease X-linked recessive 4,
+BMGC_DS07618,BMG_DS028436,722381004,Crome syndrome,,,,,,,C0795914,C536216,218900,MONDO:0009045,cataract-nephropathy-encephalopathy syndrome,"Congenital cataract, nephropathy, encephalopathy syndrome (disorder) | Congenital cataract, nephropathy, encephalopathy syndrome | Crome syndrome"
+BMGC_DS07619,BMG_DS028437,,Winter Shortland Temple syndrome,,,,,,,C0795915,C536735,601707,MONDO:0011134,Curry-Jones syndrome,
+BMGC_DS07620,BMG_DS028438,,"Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type",,,,,,,C0795917,C563050,141750,MONDO:0007716,alpha thalassemia-intellectual disability syndrome type 1,
+BMGC_DS07621,BMG_DS028440,,"Deafness, congenital onychodystrophy, recessive form",,,,,DOID:0111627,DOORS syndrome,C0795927,C538204,,,,
+BMGC_DS07622,BMG_DS028441,,Edinburgh Malformation Syndrome,,,,,,,C0795933,C563051,129850,MONDO:0007519,Edinburgh malformation syndrome,
+BMGC_DS07623,BMG_DS028442,,Digitorenocerebral Syndrome,,,,,,,C0795934,C563052,220500,MONDO:0009079,DOORS syndrome,
+BMGC_DS07624,BMG_DS028444,,AMINOPTERIN SYNDROME SINE AMINOPTERIN,,,,,,,C0795939,,600325,MONDO:0010865,pseudoaminopterin syndrome,
+BMGC_DS07625,BMG_DS028445,720954000,Filippi syndrome,,,,,DOID:0112194,Filippi syndrome,C0795940,C538152,272440,MONDO:0010092,Filippi syndrome,"Filippi syndrome (disorder) | Filippi syndrome | Type 1 syndactyly, microcephaly, intellectual disability syndrome"
+BMGC_DS07626,BMG_DS028446,,Fine-Lubinsky syndrome,,,,,,,C0795941,C537933,601353,MONDO:0011049,Fine-Lubinsky syndrome,
+BMGC_DS07627,BMG_DS028448,720957007,Fountain syndrome,,,,,,,C0795944,C537270,229120,MONDO:0009241,fountain syndrome,"Deafness with skeletal dysplasia and lip granuloma syndrome (disorder) | Fountain syndrome | Deafness with skeletal dysplasia and lip granuloma syndrome | Deafness, skeletal dysplasia, coarse face with full lips syndrome"
+BMGC_DS07628,BMG_DS028450,721297008,Galloway Mowat syndrome,,,,,DOID:0080694,Galloway-Mowat syndrome,C0795949,C537548,,MONDO:0009627,Galloway-Mowat syndrome,"Galloway Mowat syndrome (disorder) | Galloway Mowat syndrome | Galloway syndrome | Microcephaly, hiatus hernia, nephrotic syndrome | Nephrosis, neuronal dysmigration syndrome"
+BMGC_DS07629,BMG_DS028451,,Corpus callosum agenesis neuronopathy,,,,,,,C0795950,C536446,218000,MONDO:0000902,agenesis of the corpus callosum with peripheral neuropathy,
+BMGC_DS07630,BMG_DS028452,,XK aprosencephaly,,,,,,,C0795952,C536767,207770,MONDO:0008811,XK aprosencephaly,
+BMGC_DS07631,BMG_DS028453,838441009,MASA syndrome,,,,,DOID:0060246,MASA syndrome,C0795953,,303350,MONDO:0010559,MASA syndrome,"MASA syndrome | MASA (mental retardation, adducted thumbs, shuffling gait, aphasia) syndrome | Intellectual disability, aphasia, shuffling gait, adducted thumbs syndrome | Mental retardation, adducted thumbs, shuffling gait, aphasia syndrome | Intellectual disability, aphasia, shuffling gait, adducted thumbs syndrome (disorder)"
+BMGC_DS07632,BMG_DS028454,702364003,Chylomicron retention disease,,5C80.1,Hypertriglyceridaemia,E78.3,DOID:0060357,chylomicron retention disease,C0795956,C535460,246700,MONDO:0009528,chylomicron retention disease,Chylomicron retention disease | Lipid transport defect of intestine | Chylomicron retention disease (disorder) | Anderson syndrome
+BMGC_DS07633,BMG_DS028455,722451006,Gomez Lopez Hernandez syndrome,,,,,,,C0795959,C537285,601853,MONDO:0011157,Gomez-Lopez-Hernandez syndrome,Gomez Lopez Hernandez syndrome (disorder) | Gomez Lopez Hernandez syndrome | Cerebellotrigeminal dermal dysplasia syndrome
+BMGC_DS07634,BMG_DS028456,,X-linked mental retardation Gustavson type,,,,,,,C0795965,C536759,309555,MONDO:0010661,"severe X-linked intellectual disability, Gustavson type",
+BMGC_DS07635,BMG_DS028457,720636001,Hardikar syndrome,,,,,,,C0795969,C535632,301068;612726,MONDO:0012997,cholestasis-pigmentary retinopathy-cleft palate syndrome,Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) | Cholestasis with pigmentary retinopathy and cleft palate syndrome | Hardikar syndrome
+BMGC_DS07636,BMG_DS028459,,,,,,,,,C0795974,,302000,MONDO:0010540,"bullous dystrophy, macular type",
+BMGC_DS07637,BMG_DS028462,718174008,Infantile striatonigral degeneration,,,,,,,C0795996,,,MONDO:0015518,infantile bilateral striatal necrosis,Infantile striatonigral degeneration (disorder) | Infantile striatonigral degeneration | Infantile bilateral striatal necrosis
+BMGC_DS07638,BMG_DS028463,,JACKSON-WEISS SYNDROME,,,,,DOID:0111337,Jackson-Weiss syndrome,C0795998,,176943;123150;136350,MONDO:0007400,Jackson-Weiss syndrome,
+BMGC_DS07639,BMG_DS028467,,Juberg-Marsidi syndrome,,,,,,,C0796003,C567476,,,,
+BMGC_DS07640,BMG_DS028468,,,,,,,DOID:0060473,Kabuki syndrome,C0796004,,,MONDO:0016512,Kabuki syndrome,
+BMGC_DS07641,BMG_DS028469,722031003,Kapur Toriello syndrome,,,,,,,C0796005,C537008,244300,MONDO:0009483,Kapur-Toriello syndrome,Kapur Toriello syndrome (disorder) | Kapur Toriello syndrome
+BMGC_DS07642,BMG_DS028470,,Kifafa seizure disorder,,,,,,,C0796010,C537708,245180,MONDO:0009497,Kifafa seizure disorder,
+BMGC_DS07643,BMG_DS028471,,Krause-Kivlin syndrome,,,,,,,C0796012,C537617,261540,MONDO:0009856,Peters plus syndrome,
+BMGC_DS07644,BMG_DS028472,,Zimmerman Laband syndrome,,,,,,,C0796013,C536725,,MONDO:0000200,Zimmermann-Laband syndrome,
+BMGC_DS07645,BMG_DS028473,,,,,,,,,C0796016,,309800,MONDO:0010671,"microphthalmia, syndromic 1",
+BMGC_DS07646,BMG_DS028474,,Spastic paraplegia 23,,,,,,,C0796019,C536859,270750,MONDO:0010046,hereditary spastic paraplegia 23,
+BMGC_DS07647,BMG_DS028475,,Lowry Maclean syndrome,,,,,,,C0796020,C537037,600252,MONDO:0010851,Lowry-MacLean syndrome,
+BMGC_DS07648,BMG_DS028476,721975004,Lowry Wood syndrome,,,,,,,C0796021,C537038,226960,MONDO:0009191,Lowry-Wood syndrome,"Epiphyseal dysplasia, microcephalus, nystagmus syndrome (disorder) | Epiphyseal dysplasia, microcephalus, nystagmus syndrome | Lowry Wood syndrome"
+BMGC_DS07649,BMG_DS028477,,Lujan Fryns syndrome,,,,,DOID:0060821,syndromic X-linked intellectual disability 14,C0796022,C537724,309520,MONDO:0010655,X-linked intellectual disability with marfanoid habitus,
+BMGC_DS07650,BMG_DS028478,,Lysine Malabsorption Syndrome,,,,,,,C0796023,C563080,247950,MONDO:0009542,lysine malabsorption syndrome,
+BMGC_DS07651,BMG_DS028479,716023007,MacDermot Winter syndrome,,,,,,,C0796024,C537714,247990,MONDO:0009543,prominent glabella-microcephaly-hypogenitalism syndrome,Prominent glabella with microcephaly and hypogenitalism syndrome (disorder) | Prominent glabella with microcephaly and hypogenitalism syndrome | MacDermot Winter syndrome
+BMGC_DS07652,BMG_DS028480,,"ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION",,,,,DOID:0050647,Arts syndrome,C0796028,,301835,MONDO:0010533,Arts syndrome,
+BMGC_DS07653,BMG_DS028481,719451006,Malouf syndrome,,,,,DOID:0111584,dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome,C0796031,C535703,212112,MONDO:0008915,dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome,Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome | Cardiogenital syndrome | Malouf syndrome | Najjar syndrome
+BMGC_DS07654,BMG_DS028482,,Malpuech facial clefting syndrome,,,,,,,C0796032,C535704,248340,MONDO:0009554,3MC syndrome 3,
+BMGC_DS07655,BMG_DS028483,,MARDEN-WALKER SYNDROME,,,,,,,C0796033,,248700;613629,MONDO:0009564,Marden-Walker syndrome,
+BMGC_DS07656,BMG_DS028485,722380003,Martsolf syndrome,,,,,DOID:0111586,Martsolf syndrome,C0796037,C536028,,MONDO:0023910,Martsolf syndrome,Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome (disorder) | Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome | Martsolf syndrome
+BMGC_DS07657,BMG_DS028487,,Reardon Wilson Cavanagh syndrome,,,,,,,C0796045,C535295,208850,MONDO:0008838,ataxia - deafness - intellectual disability syndrome,
+BMGC_DS07658,BMG_DS028488,715428003,Gurrieri Sammito Bellussi syndrome,,,,,,,C0796046,C537625,601187,MONDO:0011011,skeletal dysplasia-epilepsy-short stature syndrome,Skeletal dysplasia with epilepsy and short stature syndrome (disorder) | Gurrieri Sammito Bellussi syndrome | Skeletal dysplasia with epilepsy and short stature syndrome
+BMGC_DS07659,BMG_DS028489,,Mercaptolactate-Cysteine Disulfiduria,,,,,,,C0796055,C563085,249650,MONDO:0009585,encephalopathy due to beta-mercaptolactate-cysteine disulfiduria,
+BMGC_DS07660,BMG_DS028491,,Mexican Cardiomelic Dysplasia,,,,,,,C0796057,C563087,249670,MONDO:0009587,mesoaxial hexadactyly and cardiac malformation,
+BMGC_DS07661,BMG_DS028492,,Oculopalatoskeletal syndrome,,,,,,,C0796059,C537738,257920,MONDO:0009770,3MC syndrome 1,
+BMGC_DS07662,BMG_DS028494,,,,,,,,,C0796063,,251255,MONDO:0009622,Jawad syndrome,
+BMGC_DS07663,BMG_DS028495,,Microcephaly cervical spine fusion anomalies,,,,,,,C0796066,C537325,251250,MONDO:0009621,microcephaly-cervical spine fusion anomalies syndrome,
+BMGC_DS07664,BMG_DS028496,,Oculodigitoesophagoduodenal syndrome,,,,,DOID:0060464,Feingold syndrome,C0796068,C537734,,MONDO:0015267,Feingold syndrome,
+BMGC_DS07665,BMG_DS028497,,"MICROPHTHALMIA, SYNDROMIC 7",,,,,,,C0796070,,309801,MONDO:0024552,linear skin defects with multiple congenital anomalies 1,
+BMGC_DS07666,BMG_DS028498,,Mirhosseini-Holmes-Walton syndrome,,,,,,,C0796072,C536438,268050,MONDO:0009986,"retinopathy, pigmentary, and intellectual disability",
+BMGC_DS07667,BMG_DS028499,,MOHR-TRANEBJAERG SYNDROME,,,,,,,C0796074,,300356;304700,MONDO:0010578,deafness dystonia syndrome,
+BMGC_DS07668,BMG_DS028503,699316006,Myhre syndrome,,,,,,,C0796081,C537620,139210,MONDO:0007688,Myhre syndrome,"Facial dysmorphism, intellectual deficit, short stature and hearing loss | Laryngotracheal stenosis, arthropathy, prognathism and short stature | Myhre syndrome | Myhre syndrome (disorder)"
+BMGC_DS07669,BMG_DS028504,719451006,Najjar syndrome,,,,,DOID:0111584,dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome,C0796083,C535580,,,,Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome | Cardiogenital syndrome | Malouf syndrome | Najjar syndrome
+BMGC_DS07670,BMG_DS028505,445257004,Nance-Horan syndrome,,,,,DOID:0060599,Nance-Horan syndrome,C0796085,C538336,302350,MONDO:0010545,Nance-Horan syndrome,Nance-Horan syndrome (disorder) | Nance-Horan syndrome
+BMGC_DS07671,BMG_DS028506,,Neuhauser syndrome,,,,,,,C0796086,C536143,249310,MONDO:0009577,megalocornea-intellectual disability syndrome,
+BMGC_DS07672,BMG_DS028508,,"LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE",,,,,DOID:0060902,Norman-Roberts syndrome,C0796089,,257320,MONDO:0009760,Norman-Roberts syndrome,
+BMGC_DS07673,BMG_DS028509,403554008,Oculocerebrocutaneous syndrome,,,,,,,C0796092,C538088,164180,MONDO:0008108,oculocerebrocutaneous syndrome,Delleman-Oorthuys syndrome | Oculocerebrocutaneous syndrome (disorder) | Oculocerebrocutaneous syndrome
+BMGC_DS07674,BMG_DS028510,,Odontoonychodermal dysplasia,,,,,,,C0796093,C537742,257980,MONDO:0009773,odonto-onycho-dermal dysplasia,
+BMGC_DS07675,BMG_DS028511,,Blepharophimosis syndrome Ohdo type,,,,,DOID:0060289,Ohdo syndrome,C0796094,C536232,249620,MONDO:0009583,"blepharophimosis - intellectual disability syndrome, Ohdo type",
+BMGC_DS07676,BMG_DS028512,,Opitz trigonocephaly syndrome,,,,,DOID:0111581,C syndrome,C0796095,C537418,211750,MONDO:0008893,C syndrome,
+BMGC_DS07677,BMG_DS028513,,CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY,,,,,,,C0796099,,216100,MONDO:0008992,Juberg-Hayward syndrome,
+BMGC_DS07678,BMG_DS028514,,Orofaciodigital Syndrome VII,,,,,DOID:0060377,orofaciodigital syndrome VII,C0796100,C563104,608518,MONDO:0012049,orofaciodigital syndrome VII,
+BMGC_DS07679,BMG_DS028515,,Orofaciodigital syndrome 8,,,,,DOID:0060378,orofaciodigital syndrome VIII,C0796101,C557820,300484,MONDO:0010336,orofaciodigital syndrome VIII,
+BMGC_DS07680,BMG_DS028516,,Orofaciodigital syndrome 9,,,,,DOID:0060382,orofaciodigital syndrome IX,C0796102,C557818,258865,MONDO:0009795,orofaciodigital syndrome IX,
+BMGC_DS07681,BMG_DS028518,,"Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor",,,,,DOID:0060476,Perlman syndrome,C0796113,C536399,267000,MONDO:0009965,Perlman syndrome,
+BMGC_DS07682,BMG_DS028519,,Pitt-Rogers-Danks Syndrome,Wolf-Hirschhorn Syndrome,,,,DOID:0050460,Wolf-Hirschhorn syndrome,C0796117,D054877,,,,
+BMGC_DS07683,BMG_DS028522,726709001,Primrose syndrome,,,,,,,C0796121,C536420,259050,MONDO:0009798,Primrose syndrome,"Intellectual disability, cataract, calcified pinna, myopathy syndrome (disorder) | Intellectual disability, cataract, calcified pinna, myopathy syndrome | Primrose syndrome"
+BMGC_DS07684,BMG_DS028523,,Cataract ataxia deafness,,,,,,,C0796123,C538283,212710,MONDO:0008928,cataract-ataxia-deafness syndrome,
+BMGC_DS07685,BMG_DS028524,,Proud Syndrome,,,,,,,C0796124,C563110,300004,MONDO:0010224,corpus callosum agenesis-abnormal genitalia syndrome,
+BMGC_DS07686,BMG_DS028525,,Absent Eyebrows and Eyelashes with Mental Retardation,,,,,,,C0796125,C563111,200130,MONDO:0008694,pseudoprogeria syndrome,
+BMGC_DS07687,BMG_DS028526,,AICARDI-GOUTIERES SYNDROME 1,,,,,,,C0796126,,606609;225750,MONDO:0009165,Aicardi-Goutieres syndrome 1,
+BMGC_DS07688,BMG_DS028527,,Ramon Syndrome,,,,,,,C0796133,C535285,266270,MONDO:0009954,Ramon syndrome,
+BMGC_DS07689,BMG_DS028528,,Renpenning syndrome 1,,,,,,,C0796135,C537761,309500,MONDO:0010653,Renpenning syndrome,
+BMGC_DS07690,BMG_DS028530,718556007,3C syndrome,,,,,DOID:0060565,Ritscher-Schinzel syndrome,C0796137,C535313,,MONDO:0019078,Ritscher-Schinzel syndrome,Craniocerebellocardiac dysplasia | Ritscher Schinzel syndrome | 3C syndrome | Cranio-cerebello-cardiac dysplasia syndrome (disorder) | Cranio-cerebello-cardiac dysplasia syndrome
+BMGC_DS07691,BMG_DS028532,,Oculodental syndrome Rutherfurd syndrome,,,,,,,C0796140,C537732,180900,MONDO:0008396,"oculodental syndrome, Rutherfurd type",
+BMGC_DS07692,BMG_DS028533,,Sao Paulo MCA-MR Syndrome,,,,,,,C0796142,C563119,268850,MONDO:0010007,microbrachycephaly-ptosis-cleft lip syndrome,
+BMGC_DS07693,BMG_DS028534,,Acrocallosal Syndrome,Acrocallosal Syndrome,,,,DOID:9250,acrocallosal syndrome,C0796147,D055673,200990,MONDO:0008708,acrocallosal syndrome,
+BMGC_DS07694,BMG_DS028535,,Scott Syndrome,,,,,DOID:0111052,Scott syndrome,C0796149,C563120,262890,MONDO:0009885,Scott syndrome,
+BMGC_DS07695,BMG_DS028536,,"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1",,,,,DOID:0060248,Simpson-Golabi-Behmel syndrome type 1,C0796154,,312870;300037,MONDO:0020602,Simpson-Golabi-Behmel syndrome type 1,
+BMGC_DS07696,BMG_DS028538,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE",,,,,,,C0796160,,300105;309583,MONDO:0010664,syndromic X-linked intellectual disability Snyder type,
+BMGC_DS07697,BMG_DS028539,715987000,Sonoda syndrome,,,,,,,C0796162,C536680,270460,MONDO:0010039,congenital heart defect-round face-developmental delay syndrome,Sonoda syndrome | Congenital heart defect with round face and developmental delay syndrome (disorder) | Congenital heart defect with round face and developmental delay syndrome
+BMGC_DS07698,BMG_DS028541,,"Spondylometaphyseal Dysplasia, X-Linked",,,,,,,C0796172,C563124,313420,MONDO:0010738,"spondylometaphyseal dysplasia, Golden type",
+BMGC_DS07699,BMG_DS028542,,Spondyloperipheral dysplasia short ulna,,,,,,,C0796173,C535799,271700,MONDO:0010078,spondyloperipheral dysplasia,
+BMGC_DS07700,BMG_DS028543,,,,,,,,,C0796176,,,MONDO:0031280,Stuve-Wiedemann syndrome,
+BMGC_DS07701,BMG_DS028544,724284005,Teebi syndrome,,,,,,,C0796179,C538387,,MONDO:0030639,Teebi hypertelorism syndrome,Hypertelorism Teebi type (disorder) | Hypertelorism Teebi type | Brachycephalofrontonasal dysplasia | Craniofrontonasal dysplasia Teebi type | Teebi hypertelorism syndrome | Teebi syndrome
+BMGC_DS07702,BMG_DS028545,715427008,Acromelic frontonasal dysplasia,,,,,,,C0796182,C535657,,,,Acromelic frontonasal dysplasia (disorder) | Acromelic frontonasal dysplasia | Toriello syndrome
+BMGC_DS07703,BMG_DS028546,,"Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence",,,,,,,C0796184,C563127,217980,MONDO:0009021,Toriello-Carey syndrome,
+BMGC_DS07704,BMG_DS028548,,Van Den Bosch Syndrome,,,,,,,C0796192,C563129,314500,MONDO:0010754,van den Bosch syndrome,
+BMGC_DS07705,BMG_DS028549,716107009,Waisman syndrome,,,,,,,C0796195,C537179,311510,MONDO:0010709,early-onset parkinsonism-intellectual disability syndrome,Early onset parkinsonism and intellectual disability syndrome (disorder) | Early onset parkinsonism and intellectual disability syndrome | Laxova Opitz syndrome | Waisman syndrome
+BMGC_DS07706,BMG_DS028550,717913006,Pashayan syndrome,,,,,,,C0796197,C536303,110050,MONDO:0007200,blepharonasofacial malformation syndrome,Blepharonasofacial malformation syndrome (disorder) | Blepharonasofacial malformation syndrome | Pashayan syndrome | Pashayan Prozansky syndrome
+BMGC_DS07707,BMG_DS028552,,,,,,,,,C0796200,,314580,MONDO:0010758,Wieacker-Wolff syndrome,
+BMGC_DS07708,BMG_DS028554,,WOODS SYNDROME,,,,,,,C0796203,,615236,MONDO:0014096,microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome,
+BMGC_DS07709,BMG_DS028555,716335003,Worster Drought syndrome,,,,,,,C0796204,C536747,185480,MONDO:0008503,Worster-Drought syndrome,Congenital suprabulbar paresis (disorder) | Congenital suprabulbar paresis | Worster Drought syndrome
+BMGC_DS07710,BMG_DS028556,,"SPINOCEREBELLAR ATAXIA, X-LINKED 1",,,,,DOID:0111829,X-linked spinocerebellar ataxia 1,C0796205,,302500;300014,MONDO:0010547,X-linked progressive cerebellar ataxia,
+BMGC_DS07711,BMG_DS028558,,,,,,,,,C0796207,,300428,MONDO:0010322,"intellectual disability, X-linked 2",
+BMGC_DS07712,BMG_DS028559,,"METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblX TYPE",,,,,DOID:0111814,methylmalonic acidemia and homocysteinemia cblX type,C0796208,,309541;300019,MONDO:0010657,"methylmalonic acidemia with homocystinuria, type cblX",
+BMGC_DS07713,BMG_DS028560,,,,,,,,,C0796215,,309549,MONDO:0010660,"intellectual disability, X-linked 9",
+BMGC_DS07714,BMG_DS028561,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 12",,,,,DOID:0112056,X-linked intellectual disability-short stature-overweight syndrome,C0796218,,300957;300395,MONDO:0010496,X-linked intellectual disability-short stature-overweight syndrome,
+BMGC_DS07715,BMG_DS028562,,,,,,,,,C0796220,,300062,MONDO:0010236,"intellectual disability, X-linked 14",
+BMGC_DS07716,BMG_DS028563,,RAYNAUD-CLAES SYNDROME,,,,,DOID:0112060,Raynaud-Claes syndrome,C0796221,,300114;302910,MONDO:0010250,"intellectual disability, X-linked 49",
+BMGC_DS07717,BMG_DS028564,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 13",,,,,,,C0796222,,300005;300055,MONDO:0010235,X-linked intellectual disability-psychosis-macroorchidism syndrome,
+BMGC_DS07718,BMG_DS028565,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 19",,,,,DOID:0112019,non-syndromic X-linked intellectual disability 19,C0796225,,300075;300844,MONDO:0010447,"intellectual disability, X-linked 19",
+BMGC_DS07719,BMG_DS028566,,,,,,,,,C0796226,,300047,MONDO:0010231,"intellectual disability, X-linked 20",
+BMGC_DS07720,BMG_DS028567,,,,,,,,,C0796229,,300046,MONDO:0010230,"intellectual disability, X-linked 23",
+BMGC_DS07721,BMG_DS028568,720565000,Bohring syndrome,,,,,,,C0796232,C537419,605039,MONDO:0011510,Bohring-Opitz syndrome,Bohring Opitz syndrome (disorder) | Bohring Opitz syndrome | C-like syndrome | Opitz trigonocephaly-like syndrome | Bohring syndrome
+BMGC_DS07722,BMG_DS028569,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 30",,,,,DOID:0112051,non-syndromic X-linked intellectual disability 30,C0796237,,300142;300558,MONDO:0010361,"intellectual disability, X-linked 30",
+BMGC_DS07723,BMG_DS028570,,CHROMOSOME Xp11.22 DUPLICATION SYNDROME,,,,,DOID:0112037,chromosome Xp11.22 duplication syndrome,C0796238,,300705,MONDO:0010406,chromosome Xp11.22 duplication syndrome,
+BMGC_DS07724,BMG_DS028571,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 29",,,,,DOID:0112021,non-syndromic X-linked intellectual disability ARX-related,C0796244,,300382;300419,MONDO:0010317,"intellectual disability, X-linked, with or without seizures, arx-related",
+BMGC_DS07725,BMG_DS028572,702412005,Partington syndrome,,,,,,,C0796250,C536300,309510,MONDO:0010654,Partington syndrome,Partington syndrome | X-linked intellectual deficit-dystonia-dysarthria syndrome (disorder) | Partington-Mulley syndrome | X-linked intellectual deficit-dystonia-dysarthria syndrome | Partington x-linked mental retardation syndrome | Partington X-linked intellectual disability syndrome
+BMGC_DS07726,BMG_DS028573,719139003,Pettigrew syndrome,,,,,DOID:0060800,syndromic X-linked intellectual disability 5,C0796254,C535773,304340,MONDO:0010574,syndromic X-linked intellectual disability 5,"X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome (disorder) | X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome | Pettigrew syndrome"
+BMGC_DS07727,BMG_DS028575,1003920007,Sabinas brittle hair syndrome,,,,,DOID:0111874,Sabinas brittle hair syndrome,C0796271,C536320,211390,MONDO:0008886,Sabinas brittle hair syndrome,Sabinas brittle hair syndrome (disorder) | Sabinas brittle hair syndrome
+BMGC_DS07728,BMG_DS028576,,,,,,,,,C0796274,,211530,MONDO:0024537,Brown-Vialetto-van Laere syndrome 1,
+BMGC_DS07729,BMG_DS028577,,Brunner Syndrome,,,,,DOID:0060693,Brunner Syndrome,C0796275,C563156,300615,MONDO:0010379,Brunner syndrome,
+BMGC_DS07730,BMG_DS028579,,Carnevale syndrome,,,,,,,C0796279,C535586,265050,MONDO:0009927,3MC syndrome 2,
+BMGC_DS07731,BMG_DS028580,720456009,Acromegaloid facial appearance syndrome,,,,,,,C0796280,C535655,102150,MONDO:0007051,acromegaloid facial appearance syndrome,Acromegaloid facial appearance syndrome (disorder) | Acromegaloid facial appearance syndrome
+BMGC_DS07732,BMG_DS028581,722379001,CAHMR syndrome,,,,,,,C0796282,C537959,211770,MONDO:0008894,cataract-hypertrichosis-intellectual disability syndrome,"Congenital cataract with hypertrichosis and intellectual disability syndrome (disorder) | Congenital cataract with hypertrichosis and intellectual disability syndrome | CAHMR syndrome | CAHMR (cataract, hypertrichosis, mental retardation) syndrome"
+BMGC_DS07733,BMG_DS028584,,,,,,,DOID:3542,adult choroid plexus cancer,C0796430,,,MONDO:0002683,adult choroid plexus neoplasm,
+BMGC_DS07734,BMG_DS028586,,,,,,,DOID:3369,Ewing sarcoma,C0796547,,,,,
+BMGC_DS07735,BMG_DS028587,,,,,,,DOID:6082,childhood testicular germ cell tumor,C0796663,,,MONDO:0003758,childhood testicular germ cell tumor,
+BMGC_DS07736,BMG_DS028588,,,,,,,DOID:6084,childhood ovarian germ cell tumor,C0796664,,,MONDO:0003760,pediatric ovarian germ cell tumor,
+BMGC_DS07737,BMG_DS028590,719097002,Branchio-skeleto-genital syndrome,,,,,,,C0809936,,211380;603463,MONDO:0008885,Elsahy-Waters syndrome,BSG syndrome | Branchio-skeleto-genital syndrome | Branchioskeletogenital syndrome | Branchioskeletogenital syndrome (disorder)
+BMGC_DS07738,BMG_DS028594,,,,,,,DOID:7474,malignant pleural mesothelioma,C0812413,,,MONDO:0005112,malignant pleural mesothelioma,
+BMGC_DS07739,BMG_DS028595,,,,,,,DOID:0060291,oculodentodigital dysplasia,C0812437,,164200,MONDO:0008111,oculodentodigital dysplasia,
+BMGC_DS07740,BMG_DS028596,,Ulnar Nerve Palsy,Ulnar Neuropathies,,,,,,C0812454,D020424,,,,
+BMGC_DS07741,BMG_DS028598,,Circadian Rhythm Disorders,Chronobiology Disorders,,,,,,C0813142,D021081,,,,
+BMGC_DS07742,BMG_DS028599,,,,,,,,,C0813230,,,MONDO:0005347,hypertriglyceridemia,
+BMGC_DS07743,BMG_DS028601,,Alcohol Related Neurodevelopmental Disorder,Fetal Alcohol Spectrum Disorders,,,,,,C0814154,D063647,,,,
+BMGC_DS07744,BMG_DS028603,165557006;79574003;415115007;6631009,Thrombocytosis,Thrombocytosis,,,D75.83,DOID:2228,thrombocytosis,C0836924,D013922,MTHU008388,MONDO:0002249,thrombocytosis disease,Thrombocythaemia | Thrombocythemia | Thrombocytosis | Thrombocythemia (finding) | Thrombocythemia | Thrombocythemia (disorder) | Thrombocythaemia | Thrombocytosis | Platelet count above reference range (finding) | Platelet count above reference range | Thrombocytosis | Increased platelets | Thrombocytosis (disorder) | Thrombocythaemia | Thrombocythemia
+BMGC_DS07745,BMG_DS028621,,Spastic quadriplegic cerebral palsy,,8D20.10,Spastic quadriplegic cerebral palsy,G80.0,,,C0837178,,,,,
+BMGC_DS07746,BMG_DS029146,251925007;840001,Rupture of bladder,,,,,,,C0840564,,,,,Rupture of bladder | Rupture of urinary bladder (disorder) | Rupture of urinary bladder | Nontraumatic rupture of bladder | Nontraumatic rupture of bladder (disorder)
+BMGC_DS07747,BMG_DS029148,,,,,,,DOID:174,acanthoma,C0846967,,,MONDO:0002093,acanthoma,
+BMGC_DS07748,BMG_DS029156,,,,,,,DOID:10892,hypospadias,C0848558,,,MONDO:0005345,hypospadias,
+BMGC_DS07749,BMG_DS029157,,,,,,,DOID:295,eye carcinoma,C0848866,,,MONDO:0002466,eye carcinoma,
+BMGC_DS07750,BMG_DS029158,,,,,,,DOID:4876,trachea carcinoma,C0848879,,,,,
+BMGC_DS07751,BMG_DS029166,721730009,Infection caused by Helicobacter pylori,,,,,,,C0850666,,,,,Infection caused by Helicobacter pylori (disorder) | Infection caused by Helicobacter pylori | Helicobacter pylori infection | Infection caused by H. pylori (Helicobacter pylori)
+BMGC_DS07752,BMG_DS029172,,,,,,,DOID:8991,cervix uteri carcinoma in situ,C0851140,,,MONDO:0042487,uterine cervix carcinoma in situ,
+BMGC_DS07753,BMG_DS029189,,Pneumocystis Infections,Pneumocystis Infections,,,,,,C0851886,D016720,,MONDO:0005923,Pneumocystis infectious disease,
+BMGC_DS07754,BMG_DS029191,,,,,,,,,C0852036,,,MONDO:0024664,"hypertension, pregnancy-induced",
+BMGC_DS07755,BMG_DS029192,,"Blood Coagulation Disorders, Inherited","Blood Coagulation Disorders, Inherited",,,,,,C0852077,D025861,,MONDO:0021181,inherited blood coagulation disorder,
+BMGC_DS07756,BMG_DS029195,,Respiratory Distress Syndrome,Respiratory Distress Syndrome,,,,,,C0852283,D012128,,,,
+BMGC_DS07757,BMG_DS029199,,Moraxella Infections,Moraxellaceae Infections,,,,,,C0852874,D045828,,MONDO:0006878,Moraxellaceae infectious disease,
+BMGC_DS07758,BMG_DS029202,,,,,,,DOID:10183,endobronchial lipoma,C0852937,,,MONDO:0000961,endobronchial lipoma,
+BMGC_DS07759,BMG_DS029209,,,,,,,DOID:3449,penis carcinoma,C0853105,,,MONDO:0006360,penile carcinoma,
+BMGC_DS07760,BMG_DS029210,,,,,,,,,C0853193,,,MONDO:0001866,bipolar I disorder,
+BMGC_DS07761,BMG_DS029211,,,,,,,DOID:3436,viral laryngitis,C0853195,,,MONDO:0002646,viral laryngitis,
+BMGC_DS07762,BMG_DS029214,,,,,,,DOID:8427,retinal melanoma,C0853394,,,MONDO:0004561,retinal melanoma,
+BMGC_DS07763,BMG_DS029215,,,,,,,DOID:5975,renal pelvis papillary tumor,C0853688,,,MONDO:0003717,renal pelvis papillary tumor,
+BMGC_DS07764,BMG_DS029218,,,,,,,,,C0853697,,,MONDO:0001475,neutropenia,
+BMGC_DS07765,BMG_DS029219,,,,,,,DOID:476,breast hemangioma,C0853715,,,MONDO:0003126,breast hemangioma,
+BMGC_DS07766,BMG_DS029222,,,,,,,,,C0853879,,,MONDO:0006256,invasive breast carcinoma,
+BMGC_DS07767,BMG_DS029223,,Diabetic Cardiomyopathies,Diabetic Cardiomyopathies,,,,,,C0853897,D058065,,,,
+BMGC_DS07768,BMG_DS029225,,Insulin-resistant diabetes mellitus,,,,,,,C0854110,,MTHU002022,,,
+BMGC_DS07769,BMG_DS029226,,Ruptured Appendicitis,Appendicitis,,,,,,C0854119,D001064,,,,
+BMGC_DS07770,BMG_DS029230,,Feeding Disorders,Feeding and Eating Disorders,,,,,,C0854145,D001068,,,,
+BMGC_DS07771,BMG_DS029231,416878008,Papillary conjunctivitis,,,,,DOID:2458,papillary conjunctivitis,C0854165,,,MONDO:0002309,papillary conjunctivitis,Papillary conjunctivitis (disorder) | Papillary conjunctivitis
+BMGC_DS07772,BMG_DS029232,,,,,,,DOID:3117,hepatobiliary benign neoplasm,C0854196,,,MONDO:0002514,hepatobiliary neoplasm,
+BMGC_DS07773,BMG_DS029233,314557000,Bacterial keratitis,,,,,,,C0854211,,,,,Bacterial keratitis | Bacterial keratitis (disorder)
+BMGC_DS07774,BMG_DS029235,425887005,Bacterial meningitis caused by Gram-negative bacteria,,,,,,,C0854215,,,MONDO:0041825,bacterial meningitis caused by gram-negative bacteria,Gram-negative bacterial meningitis | Meningitis with gram negative bacteria | Bacterial meningitis caused by Gram-negative bacteria (disorder) | Bacterial meningitis caused by Gram-negative bacteria
+BMGC_DS07775,BMG_DS029237,430395005,Pneumonia caused by Gram negative bacteria,,,,,,,C0854248,,,MONDO:0041850,pneumonia caused by gram negative bacteria,Gram negative pneumonia | Pneumonia caused by Gram negative bacteria (disorder) | Pneumonia caused by Gram negative bacteria | Pneumonia caused by Gram-negative bacteria
+BMGC_DS07776,BMG_DS029238,423451008,Infection caused by anaerobic bacteria,,,,,,,C0854328,,,MONDO:0024389,anaerobic bacteria infectious disease,Anaerobic bacterial infection | Infection caused by anaerobic bacteria (disorder) | Infection caused by anaerobic bacteria
+BMGC_DS07777,BMG_DS029240,,,,,,,DOID:9123,eczema herpeticum,C0854331,,,MONDO:0004712,herpes simplex dermatitis,
+BMGC_DS07778,BMG_DS029245,,,,,,,DOID:5395,functioning pituitary adenoma,C0854486,,,MONDO:0003429,functioning pituitary gland adenoma,
+BMGC_DS07779,BMG_DS029253,,,,,,,,,C0854699,,190330,MONDO:0008593,trichomegaly,
+BMGC_DS07780,BMG_DS029255,,Retinal Dystrophies,Retinal Dystrophies,,,,DOID:8501,fundus dystrophy,C0854723,D058499,,MONDO:0019118,inherited retinal dystrophy,
+BMGC_DS07781,BMG_DS029256,,,,,,,DOID:3571,liver cancer,C0854795,,,,,
+BMGC_DS07782,BMG_DS029257,,,,,,,DOID:7936,refractory T lymphoblastic leukemia/lymphoma,C0854859,,,MONDO:0004404,refractory precursor T-lymphoblastic lymphoma/leukemia,
+BMGC_DS07783,BMG_DS029258,,,,,,,DOID:6201,pericardial mesothelioma,C0854883,,,,,
+BMGC_DS07784,BMG_DS029259,,,,,,,DOID:1788,peritoneal mesothelioma,C0854886,,,,,
+BMGC_DS07785,BMG_DS029260,,,,,,,DOID:0001816,angiosarcoma,C0854893,,,,,
+BMGC_DS07786,BMG_DS029261,,,,,,,DOID:7428,pineal region germinoma,C0854912,,,MONDO:0004216,pineal region germinoma,
+BMGC_DS07787,BMG_DS029262,,,,,,,DOID:4650,bilateral retinoblastoma,C0854914,,,MONDO:0003075,bilateral retinoblastoma,
+BMGC_DS07788,BMG_DS029263,,,,,,,DOID:4651,unilateral retinoblastoma,C0854915,,,MONDO:0003076,unilateral retinoblastoma,
+BMGC_DS07789,BMG_DS029264,,,,,,,DOID:3674,kidney rhabdoid cancer,C0854917,,,MONDO:0002729,rhabdoid tumor of the kidney,
+BMGC_DS07790,BMG_DS029265,,,,,,,DOID:14491,regional ureteric cancer,C0854921,,,MONDO:0001978,regional ureteric cancer,
+BMGC_DS07791,BMG_DS029266,,,,,,,DOID:5750,endometrial serous adenocarcinoma,C0854924,,,MONDO:0006196,endometrial serous adenocarcinoma,
+BMGC_DS07792,BMG_DS029267,,,,,,,DOID:0050619,paranasal sinus cancer,C0854995,,,MONDO:0000380,paranasal sinus carcinoma,
+BMGC_DS07793,BMG_DS029268,,,,,,,DOID:4388,bone peripheral neuroepithelioma,C0855009,,,MONDO:0002981,peripheral primitive neuroectodermal tumor of bone,
+BMGC_DS07794,BMG_DS029269,,,,,,,DOID:5862,localized chondrosarcoma,C0855011,,,MONDO:0003682,localized chondrosarcoma,
+BMGC_DS07795,BMG_DS029270,,,,,,,DOID:3357,extraosseous osteosarcoma,C0855052,,,MONDO:0002621,extraosseous osteosarcoma,
+BMGC_DS07796,BMG_DS029272,,,,,,,,,C0855112,,,MONDO:0000901,relapsed/refractory diffuse large B-cell lymphoma,
+BMGC_DS07797,BMG_DS029274,,,,,,,DOID:3308,embryonal carcinoma,C0855159,,,,,
+BMGC_DS07798,BMG_DS029275,,,,,,,DOID:5563,malignant teratoma,C0855163,,,MONDO:0024857,immature extragonadal teratoma,
+BMGC_DS07799,BMG_DS029276,,,,,,,DOID:2024,placental choriocarcinoma,C0855173,,,MONDO:0006374,placental choriocarcinoma,
+BMGC_DS07800,BMG_DS029277,,,,,,,DOID:5556,testicular malignant germ cell cancer,C0855197,,,MONDO:0003510,malignant testicular germ cell tumor,
+BMGC_DS07801,BMG_DS029286,425748003;195951007,Acute exacerbation of chronic bronchitis,,,,,,,C0856695,,,,,Acute exacerbation of chronic bronchitis (disorder) | Acute exacerbation of chronic bronchitis | Acute exacerbation of chronic obstructive airways disease | Acute exacerbation of chronic obstructive pulmonary disease | Acute exacerbation of COPD (chronic obstructive pulmonary disease) | Acute exacerbation of chronic obstructive pulmonary disease (disorder)
+BMGC_DS07802,BMG_DS029288,426948001,Aneurysm of descending aorta,,,,,,,C0856750,,MTHU060236,,,Aneurysm of descending aorta (disorder) | Aneurysm of descending aorta
+BMGC_DS07803,BMG_DS029290,,Budd-Chiari Syndrome,Budd-Chiari Syndrome,,,,,,C0856761,D006502,600880,MONDO:0010947,Budd-Chiari syndrome,
+BMGC_DS07804,BMG_DS029293,,,,,,,DOID:2833,dehydration polycythemia,C0856815,,,MONDO:0002437,dehydration polycythemia,
+BMGC_DS07805,BMG_DS029294,,,,,,,DOID:8431,physiological polycythemia,C0856817,,,MONDO:0004563,physiological polycythemia,
+BMGC_DS07806,BMG_DS029295,,,,,,,DOID:2835,polycythemia due to hypoxia,C0856818,,,MONDO:0005572,polycythemia due to hypoxia,
+BMGC_DS07807,BMG_DS029296,,,,,,,,,C0856825,,,MONDO:0020546,acute graft versus host disease,
+BMGC_DS07808,BMG_DS029297,,Chondrocalcinosis 2,,,,,,,C0856830,C563162,118600,MONDO:0007319,chondrocalcinosis 2,
+BMGC_DS07809,BMG_DS029299,,,,,,,DOID:492,acquired hemangioma,C0856897,,,MONDO:0003206,acquired hemangioma,
+BMGC_DS07810,BMG_DS029300,,,,,,,DOID:2687,skin sarcoma,C0856900,,,MONDO:0006414,skin sarcoma,
+BMGC_DS07811,BMG_DS029301,,Retinol Deficiency,,,,,,,C0856901,C536156,,,,
+BMGC_DS07812,BMG_DS029304,,"Hyperbilirubinemia, Neonatal","Hyperbilirubinemia, Neonatal",,,,,,C0857007,D051556,,,,
+BMGC_DS07813,BMG_DS029314,,Staphylococcus Aureus Pneumonia,"Pneumonia, Staphylococcal",,,,,,C0857862,D011023,,MONDO:0041879,staphylococcus aureus pneumonia,
+BMGC_DS07814,BMG_DS029316,,,,,,,DOID:3458,breast adenocarcinoma,C0858252,,,MONDO:0004988,breast adenocarcinoma,
+BMGC_DS07815,BMG_DS029317,,,,,,,,,C0858617,,,MONDO:0020378,early-onset posterior polar cataract,
+BMGC_DS07816,BMG_DS029318,,Dyschromatopsia,,,,,,,C0858618,,MTHU002533,,,
+BMGC_DS07817,BMG_DS029319,,"Blindness, Cortical, Transient","Blindness, Cortical",,,,,,C0858621,D019575,,,,
+BMGC_DS07818,BMG_DS029323,,,,,,,DOID:4781,diffuse glomerulonephritis,C0859036,,,MONDO:0003137,diffuse glomerulonephritis,
+BMGC_DS07819,BMG_DS029327,,,,,,,DOID:5375,hair follicle neoplasm,C0859920,,,MONDO:0003413,hair follicle neoplasm,
+BMGC_DS07820,BMG_DS029329,,,,,,,DOID:625,transient hypogammaglobulinemia,C0859960,,,MONDO:0003827,transient hypogammaglobulinemia,
+BMGC_DS07821,BMG_DS029330,715192004,Idiopathic achalasia of esophagus,,,,,,,C0859976,,,MONDO:0019635,idiopathic achalasia,Idiopathic achalasia of esophagus (disorder) | Idiopathic achalasia of esophagus | Idiopathic achalasia of oesophagus | Idiopathic achalasia | Primary achalasia | Achalasia cardia
+BMGC_DS07822,BMG_DS029331,,Vaginal Yeast Infections,"Candidiasis, Vulvovaginal",,,,,,C0860029,D002181,,,,
+BMGC_DS07823,BMG_DS029333,,,,,,,,,C0860158,,,MONDO:0019155,Leydig cell hypoplasia,
+BMGC_DS07824,BMG_DS029336,,Cholestatic liver disease,,,,,,,C0860204,,MTHU026268,,,
+BMGC_DS07825,BMG_DS029337,,Drug-Induced Liver Disease,Chemical and Drug Induced Liver Injury,,,,,,C0860207,D056486,,MONDO:0005359,drug-induced liver injury,
+BMGC_DS07826,BMG_DS029339,,"Hernia, Double Inguinal",,,,,,,C0860251,C563164,142350,MONDO:0007720,"hernia, double inguinal",
+BMGC_DS07827,BMG_DS029342,450887006,Retinoic acid syndrome,,,,,,,C0860564,,,,,Retinoic acid syndrome (disorder) | Retinoic acid syndrome | Differentiation syndrome
+BMGC_DS07828,BMG_DS029343,,,,,,,DOID:5605,breast medullary carcinoma,C0860580,,,MONDO:0005063,medullary breast carcinoma,
+BMGC_DS07829,BMG_DS029348,,,,,,,DOID:3010,lobular neoplasia,C0861352,,,MONDO:0002486,lobular neoplasia,
+BMGC_DS07830,BMG_DS029349,,,,,,,DOID:5624,adenosquamous bile duct carcinoma,C0861854,,,MONDO:0003549,adenosquamous bile duct carcinoma,
+BMGC_DS07831,BMG_DS029350,,,,,,,DOID:7032,bile duct clear cell adenocarcinoma,C0861855,,,MONDO:0004081,extrahepatic bile duct clear cell adenocarcinoma,
+BMGC_DS07832,BMG_DS029351,,,,,,,DOID:3698,bile duct mucinous adenocarcinoma,C0861856,,,MONDO:0002739,extrahepatic bile duct mucinous adenocarcinoma,
+BMGC_DS07833,BMG_DS029352,,,,,,,DOID:6931,papillary extrahepatic bile duct adenocarcinoma,C0861858,,,MONDO:0004039,papillary extrahepatic bile duct adenocarcinoma,
+BMGC_DS07834,BMG_DS029353,,,,,,,DOID:3494,bile duct signet ring cell carcinoma,C0861859,,,MONDO:0002664,extrahepatic bile duct signet ring cell carcinoma,
+BMGC_DS07835,BMG_DS029354,,,,,,,DOID:5537,squamous cell bile duct carcinoma,C0861861,,,MONDO:0003500,squamous cell bile duct carcinoma,
+BMGC_DS07836,BMG_DS029355,,,,,,,DOID:0080630,B-lymphoblastic leukemia/lymphoma,C0862030,,,,,
+BMGC_DS07837,BMG_DS029357,,,,,,,DOID:4489,malignant epithelial mesothelioma,C0862312,,,MONDO:0005599,malignant epithelioid mesothelioma,
+BMGC_DS07838,BMG_DS029359,,,,,,,DOID:4013,urethra transitional cell carcinoma,C0863015,,,MONDO:0002836,urethra transitional cell carcinoma,
+BMGC_DS07839,BMG_DS029360,,,,,,,DOID:14544,rete testis adenocarcinoma,C0863024,,,MONDO:0001992,rete testis adenocarcinoma,
+BMGC_DS07840,BMG_DS029361,,,,,,,DOID:4756,testicular Leydig cell tumor,C0863027,,,MONDO:0003124,testicular Leydig cell tumor,
+BMGC_DS07841,BMG_DS029362,,,,,,,DOID:3369,Ewing sarcoma,C0863029,,,,,
+BMGC_DS07842,BMG_DS029386,,Polycythemia due to fall in plasma volume,,3A81.Z,"Acquired polycythaemia, unspecified",D75.1,DOID:0060474,familial erythrocytosis 2,C0865275,,,,,
+BMGC_DS07843,BMG_DS029389,,Idiopathic Parkinsonism or Parkinson's disease,,,,G20,DOID:0060891;DOID:0060896;DOID:0060895,Parkinson's disease 19A | Parkinson's disease 23 | Parkinson's disease 4,C0865475,,,,,
+BMGC_DS07844,BMG_DS029390,,Primary Parkinsonism or Parkinson's disease,,,,G20,DOID:0060891;DOID:0060896;DOID:0060895,Parkinson's disease 19A | Parkinson's disease 23 | Parkinson's disease 4,C0865476,,,,,
+BMGC_DS07845,BMG_DS029402,,,,,,,DOID:5641,diffuse pulmonary fibrosis,C0865849,,,MONDO:0003563,diffuse pulmonary fibrosis,
+BMGC_DS07846,BMG_DS029415,402356004,Chronic graft-versus-host disease,,,,D89.811,,,C0867389,,,MONDO:0020547,chronic graft versus host disease,Chronic graft-versus-host disease (disorder) | Chronic graft-versus-host disease | Chronic graft versus host disease
+BMGC_DS07847,BMG_DS029420,240307008,Late neonatal hypocalcemia,,,,,,,C0869150,,,,,Late neonatal hypocalcemia | Hypocalcaemic tetany in newborn | Late neonatal hypocalcaemia | Hypocalcemic tetany in newborn | Late neonatal hypocalcemia (disorder)
+BMGC_DS07848,BMG_DS029425,399617002,Carditis,Myocarditis,,,,,,C0869523,D009205,,MONDO:0024636,inflammation of heart layer,Carditis (disorder) | Carditis
+BMGC_DS07849,BMG_DS029429,201059003;238623003;26996000;20637002;396228006,Hyperkeratosis,,,,,,,C0870082,,MTHU001049,,,Hyperkeratosis | Hyperkeratosis (disorder) | Hyperkeratosis | Keratosis | Excessive cornification | Skin callus | Callosity | Keratoma | Tyloma | Tylosis | Hyperkeratosis (morphologic abnormality) | Hyperkeratosis of skin | Acquired keratoderma palmaris et plantaris | Keratoderma climactericum | Hyperkeratosis palmoplantaris climacterica | HK - Hyperkeratosis | Acquired keratosis palmaris et plantaris | Hyperkeratosis | Hyperkeratosis (disorder) | Hyperkeratosis (disorder) | Hyperkeratosis | HK - Hyperkeratosis | Hyperkeratosis of skin
+BMGC_DS07850,BMG_DS029433,772791006,Sarcopenia,Sarcopenia,,,M62.84,,,C0872084,D055948,,MONDO:0006516,obsolete sarcopenia,Sarcopenia | Sarcopenia (disorder) | Loss of skeletal muscle mass
+BMGC_DS07851,BMG_DS029434,,,,,,,,,C0872218,,,MONDO:0017575,mitochondrial neurogastrointestinal encephalomyopathy,
+BMGC_DS07852,BMG_DS029440,,,,,,,DOID:0060490,Schimke immuno-osseous dysplasia,C0877024,,242900,MONDO:0009458,Schimke immuno-osseous dysplasia,
+BMGC_DS07853,BMG_DS029449,,Patellofemoral Pain Syndrome,Patellofemoral Pain Syndrome,,,,DOID:14284,patellofemoral pain syndrome,C0877149,D046788,,MONDO:0006894,patellofemoral pain syndrome,
+BMGC_DS07854,BMG_DS029450,,,,,,,DOID:4037,necrotizing gastritis,C0877152,,,MONDO:0002845,necrotizing gastritis,
+BMGC_DS07855,BMG_DS029454,,Peripartum cardiomyopathy,,JB44.3,Cardiomyopathy in the puerperium,O90.3,DOID:9997,peripartum cardiomyopathy,C0877208,,,MONDO:0018920,peripartum cardiomyopathy,
+BMGC_DS07856,BMG_DS029460,,,,,,,DOID:8433,thyroid malformation,C0877367,,,MONDO:0004564,thyroid malformation,
+BMGC_DS07857,BMG_DS029461,,,,,,,DOID:6621,cerebral angioma,C0877388,,,MONDO:0003948,cerebral hemangioma,
+BMGC_DS07858,BMG_DS029464,,Exostoses Of Heel,,,,,,,C0877431,C563167,133600,MONDO:0007583,obsolete exostoses of heel,
+BMGC_DS07859,BMG_DS029466,432261003,Candidemia,Candidemia,,,,,,C0877445,D058387,,MONDO:0044070,candidemia,Candidemia (disorder) | Candidemia
+BMGC_DS07860,BMG_DS029469,,,,,,,DOID:7320,ovarian serous cystadenofibroma,C0877572,,,MONDO:0004185,ovarian serous cystadenofibroma,
+BMGC_DS07861,BMG_DS029470,,,,,,,DOID:4413,cervix melanoma,C0877611,,,MONDO:0002988,cervix melanoma,
+BMGC_DS07862,BMG_DS029473,,,,,,,DOID:3369,Ewing sarcoma,C0877849,,,MONDO:0006094,Askin tumor,
+BMGC_DS07863,BMG_DS029474,,Cerebral Arteriosclerosis,Intracranial Arteriosclerosis,,,,,,C0877854,D002537,,,,
+BMGC_DS07864,BMG_DS029475,,Cerebral Embolism and Thrombosis,Intracranial Embolism and Thrombosis,,,,,,C0877855,D002542,,,,
+BMGC_DS07865,BMG_DS029476,,,,,,,DOID:6004,aleukemic leukemia,C0877858,,,MONDO:0003730,aleukemic leukemia,
+BMGC_DS07866,BMG_DS029478,17941002,Arteriolosclerosis,Arteriolosclerosis,,,,DOID:5162,arteriolosclerosis,C0878486,D050379,,MONDO:0006658,arteriolosclerosis,Arteriolosclerosis | Arteriolosclerosis (morphologic abnormality)
+BMGC_DS07867,BMG_DS029483,,Cardiomyopathies,Cardiomyopathies,,,,DOID:0050700,cardiomyopathy,C0878544,D009202,,MONDO:0004994,cardiomyopathy,
+BMGC_DS07868,BMG_DS029484,430476004,Diffuse panbronchiolitis,,,,,,,C0878555,C536174,604809,MONDO:0011490,diffuse panbronchiolitis,Diffuse panbronchiolitis (disorder) | Diffuse panbronchiolitis
+BMGC_DS07869,BMG_DS029486,,Posterior Leukoencephalopathy Syndrome,Posterior Leukoencephalopathy Syndrome,,,,,,C0878576,D054038,,MONDO:0044033,posterior leukoencephalopathy syndrome,
+BMGC_DS07870,BMG_DS029488,,,,,,,,,C0878587,,243400,MONDO:0009472,"acetylation, slow",
+BMGC_DS07871,BMG_DS029489,,Sphincter of Oddi Dysfunction,Sphincter of Oddi Dysfunction,,,,,,C0878588,D046628,,,,
+BMGC_DS07872,BMG_DS029492,,Erdheim-Chester Disease,Erdheim-Chester Disease,,,,DOID:4329,Erdheim-Chester disease,C0878675,D031249,,MONDO:0018153,Erdheim-Chester disease,
+BMGC_DS07873,BMG_DS029493,,6-pyruvoyl-tetrahydropterin synthase deficiency,,,,,DOID:0090106,BH4-deficient hyperphenylalaninemia A,C0878676,C535325,261640,MONDO:0009863,BH4-deficient hyperphenylalaninemia A,
+BMGC_DS07874,BMG_DS029494,,Glycogen Storage Disease Type IIb,Glycogen Storage Disease Type IIb,,,,DOID:0050437,Danon disease,C0878677,D052120,300257,MONDO:0010281,Danon disease,
+BMGC_DS07875,BMG_DS029495,444645005,Dent's disease,,,,,DOID:0050699,Dent disease,C0878681,,,MONDO:0015612,Dent disease,Dent's disease (disorder) | Dent disease | Dent's disease
+BMGC_DS07876,BMG_DS029496,124224004,Deficiency of ferroxidase (disorder),,,,,,,C0878682,,604290,MONDO:0011426,aceruloplasminemia,Deficiency of ceruloplasmin | Deficiency of ferroxidase | Deficiency of caeruloplasmin | Deficiency of ferroxidase (disorder)
+BMGC_DS07877,BMG_DS029497,,,,,,,,,C0878683,,262600,MONDO:0009878,"pituitary hormone deficiency, combined, 2",
+BMGC_DS07878,BMG_DS029498,,SHORT syndrome,,,,,DOID:0111454,SHORT syndrome,C0878684,C537327,269880,MONDO:0010026,SHORT syndrome,
+BMGC_DS07879,BMG_DS029499,408663001,Conjunctivochalasis,,,,H11.82,DOID:4250,conjunctivochalasis,C0878693,,,MONDO:0002931,conjunctivochalasis,Conjunctivochalasis (disorder) | Conjunctivochalasis | Chronic localized conjunctival chemosis | Chronic localised conjunctival chemosis
+BMGC_DS07880,BMG_DS029503,,Synovial Plica Syndrome,Synovitis,,,,DOID:12225,Plica syndrome,C0878705,D013585,,,,
+BMGC_DS07881,BMG_DS029504,,Overactive Bladder,"Urinary Bladder, Overactive",,,,DOID:0070355,overactive bladder syndrome,C0878773,D053201,,MONDO:0006624,overactive bladder,
+BMGC_DS07882,BMG_DS029506,,,,,,,DOID:6163,familial renal papillary carcinoma,C0879257,,605074,MONDO:0003789,hereditary papillary renal cell carcinoma,
+BMGC_DS07883,BMG_DS029507,,,,,,,DOID:6244,familial renal oncocytoma,C0879606,,,MONDO:0003824,hereditary kidney oncocytoma,
+BMGC_DS07884,BMG_DS029508,,Posterior Choroidal Artery Infarction,Cerebral Infarction,,,,,,C0887799,D002544,,,,
+BMGC_DS07885,BMG_DS029510,,,,,,,DOID:3587,pancreatic ductal carcinoma,C0887833,,,,,
+BMGC_DS07886,BMG_DS029511,,,,,,,DOID:6003,aleukemic leukemia cutis,C0887846,,,MONDO:0003729,aleukemic leukemia cutis,
+BMGC_DS07887,BMG_DS029512,,"Polycystic Kidney, Type 1 Autosomal Dominant Disease","Polycystic Kidney, Autosomal Dominant",,,,,,C0887850,D016891,174050,MONDO:0008265,polycystic liver disease 1,
+BMGC_DS07888,BMG_DS029516,,Becker Muscular Dystrophy,"Muscular Dystrophy, Duchenne",,,,,,C0917713,D020388,300376,MONDO:0010311,Becker muscular dystrophy,
+BMGC_DS07889,BMG_DS029517,,Hajdu-Cheney Syndrome,Hajdu-Cheney Syndrome,,,,DOID:2736,Hajdu-Cheney syndrome,C0917715,D031845,102500,MONDO:0007057,Acroosteolysis dominant type,
+BMGC_DS07890,BMG_DS029518,,Pulmonic Plague,Plague,,,,,,C0917716,D010930,,,,
+BMGC_DS07891,BMG_DS029519,,"Optic Atrophy, Hereditary, Leber","Optic Atrophy, Hereditary, Leber",,,,DOID:705,Leber hereditary optic neuropathy,C0917796,D029242,535000,MONDO:0010788,Leber hereditary optic neuropathy,
+BMGC_DS07892,BMG_DS029520,,,,,,,,,C0917798,,,MONDO:0005299,brain ischemia,
+BMGC_DS07893,BMG_DS029521,77692006,Hypersomnia,Disorders of Excessive Somnolence,7A21,Idiopathic hypersomnia,G47.1,,,C0917799,D006970,MTHU062007,MONDO:0005466,hypersomnia,Hypersomnia | Hypersomnia (disorder) | Excessive sleep | Sleeps too much | Excessive sleepiness | Hypersomnia (excessive sleeping)
+BMGC_DS07894,BMG_DS029522,,"Epilepsy, Myoclonic, Infantile","Epilepsies, Myoclonic",,,,,,C0917800,D004831,605021,MONDO:0011506,familial infantile myoclonic epilepsy,
+BMGC_DS07895,BMG_DS029523,,,,,,,,,C0917801,,,MONDO:0013600,insomnia,
+BMGC_DS07896,BMG_DS029524,,,,,,,,,C0917804,,108010,MONDO:0007154,arteriovenous malformations of the brain,
+BMGC_DS07897,BMG_DS029525,,Transient Cerebral Ischemia,"Ischemic Attack, Transient",,,,,,C0917805,D002546,,,,
+BMGC_DS07898,BMG_DS029526,,Haemophilus influenzae Meningitis Type B,"Meningitis, Haemophilus",,,,DOID:0080179,haemophilus meningitis,C0917807,D008583,,,,
+BMGC_DS07899,BMG_DS029528,,Nerve Entrapment,Nerve Compression Syndromes,,,,,,C0917811,D009408,,,,
+BMGC_DS07900,BMG_DS029529,,Tetanilla,Tetany,,,,,,C0917812,D013746,,,,
+BMGC_DS07901,BMG_DS029531,,,,,,,DOID:13185,esophageal diverticulosis,C0917875,,,MONDO:0006754,esophageal diverticulosis,
+BMGC_DS07902,BMG_DS029534,,Progressive Muscular Atrophy,"Muscular Atrophy, Spinal",,,,DOID:318,progressive muscular atrophy,C0917981,D009134,,,,
+BMGC_DS07903,BMG_DS029535,,Acro-Osteolysis,Acro-Osteolysis,,,,DOID:2736,Hajdu-Cheney syndrome,C0917990,D030981,102400,MONDO:0007056,acroosteolysis,
+BMGC_DS07904,BMG_DS029536,,Cerebral Aneurysm,Intracranial Aneurysm,,,,,,C0917996,D002532,,,,
+BMGC_DS07905,BMG_DS029537,,,,,,,DOID:2394,ovarian cancer,C0919267,,,MONDO:0021068,ovarian neoplasm,
+BMGC_DS07906,BMG_DS029538,,Decreased Intraocular Pressure-Associated Papilledema,Papilledema,,,,DOID:10175,optic papillitis,C0919308,D010211,,,,
+BMGC_DS07907,BMG_DS029542,,"Upper Extremity Deep Vein Thrombosis, Primary",Upper Extremity Deep Vein Thrombosis,,,,,,C0919631,D056824,,,,
+BMGC_DS07908,BMG_DS029543,,,,,,,DOID:4638,postauricular lymphadenitis,C0919638,,,MONDO:0003068,postauricular lymphadenitis,
+BMGC_DS07909,BMG_DS029548,,Cytokine Storm,Cytokine Release Syndrome,,,,,,C0919747,D000080424,,,,
+BMGC_DS07910,BMG_DS029549,,,,,,,DOID:4640,axillary adenitis,C0919797,,,MONDO:0003070,axillary lymphadenitis,
+BMGC_DS07911,BMG_DS029560,,,,,,,DOID:6425,eyelid carcinoma,C0920196,,,MONDO:0003876,eyelid carcinoma,
+BMGC_DS07912,BMG_DS029562,,,,,,,DOID:5271,small intestine leiomyosarcoma,C0920305,,,MONDO:0003360,small intestine leiomyosarcoma,
+BMGC_DS07913,BMG_DS029564,,,,,,,DOID:5684,"spondyloepimetaphyseal dysplasia, Sponastrime type",C0920349,,,,,
+BMGC_DS07914,BMG_DS029565,21983002;66944004;190297000,Autoimmune thyroiditis,,5A03.2Z,"Autoimmune thyroiditis, unspecified",E06.3,DOID:7188,autoimmune thyroiditis,C0920350,,MTHU037300,MONDO:0005623,autoimmune thyroid disease,Hashimoto thyroiditis | Autoimmune lymphocytic chronic thyroiditis | Lymphocytic thyroiditis | Struma lymphomatosa | Hashimoto's disease | Struma lymphomatosis | Chronic lymphocytic thyroiditis | Hashimoto's thyroiditis | Hashimoto thyroiditis (disorder) | Autoimmune thyroiditis | Autoimmune thyroiditis (disorder) | Hashimoto's disease | Autoimmune thyroiditis | Chronic lymphocytic thyroiditis | Thyroiditis: [chronic lymphocytic] or [autoimmune] or [Hashimoto's] | Thyroiditis: [chronic lymphocytic] or [autoimmune] or [Hashimoto's] (disorder)
+BMGC_DS07915,BMG_DS029569,,Testicular Feminization,Androgen-Insensitivity Syndrome,,,,DOID:0080775,complete androgen insensitivity syndrome,C0936016,D013734,,MONDO:0021023,complete androgen insensitivity syndrome,
+BMGC_DS07916,BMG_DS029570,,Vitamin B 6 Deficiency,Vitamin B 6 Deficiency,,,,DOID:8455,pyridoxine deficiency anemia,C0936215,D026681,,,,
+BMGC_DS07917,BMG_DS029572,,HIV-1-Associated Cognitive Motor Complex,AIDS Dementia Complex,,,,,,C0936243,D015526,,,,
+BMGC_DS07918,BMG_DS029574,,Brain Embolism and Thrombosis,Intracranial Embolism and Thrombosis,,,,,,C0936247,D002542,,,,
+BMGC_DS07919,BMG_DS029575,,,,,,,DOID:2602,chondroma,C0936248,,,MONDO:0002360,chondroma,
+BMGC_DS07920,BMG_DS029576,,Eczema Herpeticum,Kaposi Varicelliform Eruption,,,,DOID:9123,eczema herpeticum,C0936250,D007617,,,,
+BMGC_DS07921,BMG_DS029577,,Polyradiculitis,Polyradiculopathy,,,,,,C0936251,D011128,,,,
+BMGC_DS07922,BMG_DS029579,,Lysine Alpha-Ketoglutarate Reductase Deficiency Disease,Hyperlysinemias,,,,,,C0936256,D020167,,,,
+BMGC_DS07923,BMG_DS029581,,Brain Thrombus,Intracranial Thrombosis,,,,,,C0936261,D020767,,,,
+BMGC_DS07924,BMG_DS029582,,Cerebral Thrombus,Intracranial Thrombosis,,,,,,C0936263,D020767,,,,
+BMGC_DS07925,BMG_DS029583,,"Familial Amyloid Polyneuropathy, Type IV","Amyloid Neuropathies, Familial",,,,,,C0936273,D028227,,,,
+BMGC_DS07926,BMG_DS029584,,,,,,,DOID:4766,embryoma,C0936282,,,MONDO:0005565,blastoma,
+BMGC_DS07927,BMG_DS029585,,,,,,,DOID:10655,lipoma of colon,C0940607,,,MONDO:0001091,lipoma of colon,
+BMGC_DS07928,BMG_DS029593,44900007;235919008,Cholecystolithiasis,Cholecystolithiasis,,,,DOID:11151,cholecystolithiasis,C0947622,D041761,,MONDO:0006698,cholecystolithiasis,Biliary calculus | Biliary calculus (disorder) | Cholecystolithiasis | Gallstones | Gallbladder stones | Gallbladder calculus | GS - Gallstone | Gallstone | Gallbladder calculus (disorder)
+BMGC_DS07929,BMG_DS029596,422504002,Ischemic stroke,,,,,,,C0948008,,MTHU000098,,,Ischemic stroke (disorder) | Ischemic stroke | Ischaemic stroke
+BMGC_DS07930,BMG_DS029597,723096000,Gastritis caused by bacterium,,,,,DOID:4033,bacterial gastritis,C0948039,,,MONDO:0002842,bacterial gastritis,Gastritis caused by bacterium (disorder) | Gastritis caused by bacterium | Bacterial gastritis
+BMGC_DS07931,BMG_DS029601,,Acute Coronary Syndrome,Acute Coronary Syndrome,,,,,,C0948089,D054058,,MONDO:0005542,acute coronary syndrome,
+BMGC_DS07932,BMG_DS029605,95434006;155627006;266411000,Tracheomalacia,Tracheomalacia,,,,,,C0948187,D055090,MTHU012591,MONDO:0019804,tracheomalacia,Tracheomalacia | Tracheomalacia (disorder) | (Respiratory disease NOS) or (adult respiratory distress syndrome) or (pneumomediastinum) or (tracheomalacia) | Resp. distress synd. - adult | Respirat distress synd-adult | Pneumomediastinum | Pmeumomediastinum | Respiratory disease NOS | Tracheomalacia | Adult respiratory distress syndrome | (Respiratory disease NOS) or (adult respiratory distress syndrome) or (pneumomediastinum) or (tracheomalacia) (disorder) | Tracheomalacia | Respirat distress synd-adult | Pmeumomediastinum | Resp. distress synd. - adult | Respiratory disease NOS | Pneumomediastinum | Adult respiratory distress syndrome | (Respiratory disease NOS) or (adult respiratory distress syndrome) or (pneumomediastinum) or (tracheomalacia) | (Respiratory disease NOS) or (adult respiratory distress syndrome) or (pneumomediastinum) or (tracheomalacia) (disorder)
+BMGC_DS07933,BMG_DS029607,1137353009,Infection caused by Citrobacter,,,,,,,C0948204,,,,,Infection caused by Citrobacter | Infection caused by Citrobacter (disorder) | Citrobacter infection
+BMGC_DS07934,BMG_DS029609,,,,,,,DOID:3713,ovary adenocarcinoma,C0948216,,,MONDO:0002752,ovarian adenocarcinoma,
+BMGC_DS07935,BMG_DS029611,,Cytokine Release Syndrome,Cytokine Release Syndrome,,,,,,C0948245,D000080424,,MONDO:0600008,cytokine release syndrome,
+BMGC_DS07936,BMG_DS029614,422773005,Hemodynamic instability,,,,,,,C0948268,,MTHU070057,,,Hemodynamic instability (finding) | Haemodynamic instability | Hemodynamic instability
+BMGC_DS07937,BMG_DS029621,,,,,,,DOID:0111255,McKusick-Kaufman syndrome,C0948368,,236700,MONDO:0009367,McKusick-Kaufman syndrome,
+BMGC_DS07938,BMG_DS029629,,Coronary Restenosis,Coronary Restenosis,,,,DOID:4247,coronary restenosis,C0948480,D023903,,MONDO:0005355,coronary restenosis,
+BMGC_DS07939,BMG_DS029635,723097009,Gastritis caused by fungus,,,,,DOID:4034,fungal gastritis,C0948638,,,MONDO:0002843,fungal gastritis,Gastritis caused by fungus (disorder) | Gastritis caused by fungus | Fungal gastritis
+BMGC_DS07940,BMG_DS029638,,,,,,,DOID:7378,pituitary hypoplasia,C0948740,,,MONDO:0004201,pituitary hypoplasia,
+BMGC_DS07941,BMG_DS029639,,,,,,,DOID:12342,retroperitoneum carcinoma,C0948749,,,MONDO:0001502,retroperitoneum carcinoma,
+BMGC_DS07942,BMG_DS029640,,,,,,,,,C0948750,,,MONDO:0000521,salivary gland carcinoma,
+BMGC_DS07943,BMG_DS029643,421807004,Gastrointestinal hypomotility,,,,,,,C0948779,,,,,Gastrointestinal hypomotility (disorder) | Gastrointestinal hypomotility
+BMGC_DS07944,BMG_DS029646,370999003,Primary hypogonadism,,,,,,,C0948896,,MTHU055789,,,Primary hypogonadism (disorder) | Primary hypogonadism | Hypergonadotropic hypogonadism
+BMGC_DS07945,BMG_DS029648,,,,,,,DOID:3013,intraductal breast benign neoplasm,C0948967,,,MONDO:0002488,intraductal breast neoplasm,
+BMGC_DS07946,BMG_DS029649,,,,,,,DOID:1993,rectum cancer,C0949022,,,MONDO:0006519,rectal cancer,
+BMGC_DS07947,BMG_DS029651,,,,,,,,,C0949059,,,MONDO:0021392,polyp of large intestine,
+BMGC_DS07948,BMG_DS029652,425464007,Hospital acquired pneumonia,,,,,,,C0949083,,,,,Nosocomial pneumonia (disorder) | Nosocomial pneumonia | Hospital acquired pneumonia | HAP - hospital acquired pneumonia
+BMGC_DS07949,BMG_DS029653,188588001;191236003,Congenital hypoplastic anemia,,,,,DOID:1342,congenital hypoplastic anemia,C0949116,,MTHU011578,,,Chronic constitutional pure red cell anemia | Congenital hypoplastic anemia | Diamond-Blackfan anemia | Familial hypoplastic anemia | Chronic constitutional pure red cell aplasia | Chronic constitutional pure red cell anaemia | Congenital hypoplastic anaemia | Diamond-Blackfan anaemia | Familial hypoplastic anaemia | Congenital erythroid hypoplasia | Congenital red cell aplasia | Diamond-Blackfan syndrome | Adenosine deaminase superactivity (disorder) | Constitutional aplastic anaemia without mention of malformation | Congenital hypoplastic anaemia | Congenital hypoplastic anemia | Constitutional aplastic anemia without mention of malformation | Anaemia: [congenital hypoplastic] or [constitutional aplastic without mention of malformation] | Anemia: [congenital hypoplastic] or [constitutional aplastic without mention of malformation] | Anaemia: [congenital hypoplastic] or [constitutional aplastic without mention of malformation] (disorder)
+BMGC_DS07950,BMG_DS029654,408669002,Acute laryngitis with obstruction,,,,,DOID:9396,acute laryngitis,C0949123,,,,,Acute laryngitis with obstruction (disorder) | Acute laryngitis with obstruction
+BMGC_DS07951,BMG_DS029664,,Ileocolitis,Crohn Disease,,,,,,C0949272,D003424,,MONDO:0005534,ileocolitis,
+BMGC_DS07952,BMG_DS029665,,,,,,,,,C0949331,,600171,MONDO:0010838,gonadal agenesis,
+BMGC_DS07953,BMG_DS029666,,Neonatal Diseases and Abnormalities,"Congenital, Hereditary, and Neonatal Diseases and Abnormalities",,,,,,C0949367,D009358,,,,
+BMGC_DS07954,BMG_DS029667,,Luft Disease,Mitochondrial Myopathies,,,,,,C0949496,D017240,,,,
+BMGC_DS07955,BMG_DS029669,201087007;80432009,Porokeratosis of Mibelli,Porokeratosis,,,,,,C0949506,D017499,MTHU048670,MONDO:0019141,porokeratosis of Mibelli,Porokeratosis of Mibelli | Porokeratosis of Mibelli (disorder) | Porokeratosis of Mibelli | Mibelli's disease | Porokeratosis of Mibelli (disorder)
+BMGC_DS07956,BMG_DS029670,,,,,,,DOID:3660,wheat allergy,C0949570,,,,,
+BMGC_DS07957,BMG_DS029671,,,,,,,DOID:14450,46 XX gonadal dysgenesis,C0949595,,233300,MONDO:0024463,ovarian dysgenesis 1,
+BMGC_DS07958,BMG_DS029673,,"Cardiomyopathy, Hypertrophic, Familial","Cardiomyopathy, Hypertrophic, Familial",,,,DOID:0080326,familial hypertrophic cardiomyopathy,C0949658,D024741,,MONDO:0024573,familial hypertrophic cardiomyopathy,
+BMGC_DS07959,BMG_DS029674,,Tauopathies,Tauopathies,,,,DOID:680,tauopathy,C0949664,D024801,,MONDO:0005574,tauopathy,
+BMGC_DS07960,BMG_DS029676,371082009,Spondylarthritis,Spondylarthritis,,,,,,C0949690,D025241,,MONDO:0001434,inflammatory spondylopathy,Arthritis of spine (disorder) | Arthritis of spine | Inflammatory spondylopathy
+BMGC_DS07961,BMG_DS029677,,Spondylarthropathies,Spondylarthropathies,,,,DOID:1123,spondyloarthropathy,C0949691,D025242,,MONDO:0005095,spondyloarthropathy,
+BMGC_DS07962,BMG_DS029678,,Polyomavirus Infections,Polyomavirus Infections,,,,,,C0949804,D027601,,MONDO:0005927,polyomavirus infectious disease,
+BMGC_DS07963,BMG_DS029679,,"Electron Transport Chain Deficiencies, Mitochondrial",Mitochondrial Diseases,,,,,,C0949855,D028361,,,,
+BMGC_DS07964,BMG_DS029680,,Oxidative Phosphorylation Deficiencies,Mitochondrial Diseases,,,,,,C0949856,D028361,,,,
+BMGC_DS07965,BMG_DS029681,,Mitochondrial Respiratory Chain Deficiencies,Mitochondrial Diseases,,,,,,C0949857,D028361,,,,
+BMGC_DS07966,BMG_DS029684,,Denys-Drash Syndrome,Denys-Drash Syndrome,,,,DOID:3764,Denys-Drash syndrome,C0950121,D030321,194080,MONDO:0008682,Denys-Drash syndrome,
+BMGC_DS07967,BMG_DS029685,,Frasier Syndrome,Frasier Syndrome,,,,DOID:0050438,Frasier syndrome,C0950122,D052159,136680,MONDO:0007635,Frasier syndrome,
+BMGC_DS07968,BMG_DS029686,,"Genetic Diseases, Inborn","Genetic Diseases, Inborn",,,,,,C0950123,D030342,,,,
+BMGC_DS07969,BMG_DS029687,30415006,Disease due to Papilloma virus,,,,,,,C0950124,,,,,Disease caused by Papilloma virus | Disease caused by Papillomavirus (disorder) | Disease caused by Papillomavirus
+BMGC_DS07970,BMG_DS029688,,Autosomal Chromosome Disorders,Chromosome Disorders,,,,,,C0969687,D025063,,,,
+BMGC_DS07971,BMG_DS029690,229653009;20301004,Dysphasia,Aphasia,,,R47.02,DOID:0060046,aphasia,C0973461,D001037,MTHU036833,,,Dysphasia | Dysphasia (disorder) | Dysphasia | Dysphasia (finding)
+BMGC_DS07972,BMG_DS029692,,Type 1 Duane Retraction Syndrome,Duane Retraction Syndrome,,,,,,C0994516,D004370,126800,MONDO:0024265,Duane syndrome type 1,
+BMGC_DS07973,BMG_DS029694,,Drug Resistant Epilepsy,Drug Resistant Epilepsy,,,,,,C1096063,D000069279,,,,
+BMGC_DS07974,BMG_DS029701,,Kinsbourne Syndrome,Opsoclonus-Myoclonus Syndrome,,,,,,C1096154,D053578,,,,
+BMGC_DS07975,BMG_DS029702,,Macrophage Activation Syndrome,Macrophage Activation Syndrome,,,,,,C1096155,D055501,,MONDO:0015545,macrophage activation syndrome,
+BMGC_DS07976,BMG_DS029712,,,,,,,DOID:1796,pancreas sarcoma,C1096346,,,MONDO:0002117,pancreas sarcoma,
+BMGC_DS07977,BMG_DS029713,,,,,,,DOID:9300,neurofibroma of the heart,C1096349,,,MONDO:0004752,neurofibroma of the heart,
+BMGC_DS07978,BMG_DS029720,135341000119101,Peptostreptococcus infection,,,,,,,C1096562,,,MONDO:0024412,Peptostreptococcus infectious disease,Peptostreptococcus infection | Peptostreptococcus infection (disorder)
+BMGC_DS07979,BMG_DS029725,,,,,,,DOID:3605,ovarian cystadenocarcinoma,C1096638,,,MONDO:0002702,ovarian cystadenocarcinoma,
+BMGC_DS07980,BMG_DS029726,,,,,,,DOID:3607,appendix mucinous cystadenocarcinoma,C1096639,,,MONDO:0002703,appendix mucinous cystadenocarcinoma,
+BMGC_DS07981,BMG_DS029731,,Infantile Sialic Acid Storage Disease,Sialic Acid Storage Disease,,,,,,C1096902,D029461,269920,MONDO:0010027,"free sialic acid storage disease, infantile form",
+BMGC_DS07982,BMG_DS029732,87074006,Salla disease,,,,,,,C1096903,,604369,MONDO:0011449,Salla disease,"Salla disease | Sialuria, Finnish type | Salla disease (disorder) | Adult sialic acid storage disease"
+BMGC_DS07983,BMG_DS029733,,,,,,,DOID:3003,nipple benign neoplasm,C1112166,,,MONDO:0002482,nipple neoplasm,
+BMGC_DS07984,BMG_DS029736,,Sensorimotor neuropathy,,,,,,,C1112256,,MTHU035590,,,
+BMGC_DS07985,BMG_DS029739,,,,,,,DOID:8133,epiglottis cancer,C1112382,,,MONDO:0004473,epiglottis cancer,
+BMGC_DS07986,BMG_DS029741,,,,,,,DOID:4389,soft tissue peripheral neuroepithelioma,C1112437,,,MONDO:0002982,peripheral primitive neuroectodermal tumor of soft tissues,
+BMGC_DS07987,BMG_DS029744,,,,,,,DOID:7134,esophagus small cell carcinoma,C1112474,,,MONDO:0004116,esophageal small cell neuroendocrine carcinoma,
+BMGC_DS07988,BMG_DS029745,,,,,,,DOID:4798,aggressive systemic mastocytosis,C1112486,,,MONDO:0020333,aggressive systemic mastocytosis,
+BMGC_DS07989,BMG_DS029747,,,,,,,DOID:9655,oral mucosa leukoplakia,C1112530,,,,,
+BMGC_DS07990,BMG_DS029748,,,,,,,DOID:0080852,paraneoplastic pemphigus,C1112570,,,MONDO:0018974,paraneoplastic pemphigus,
+BMGC_DS07991,BMG_DS029750,,Granulomatous gastritis,,DA42.Z,"Gastritis, unspecified",K29.6,DOID:4038,granulomatous gastritis,C1112577,,,MONDO:0002846,granulomatous gastritis,
+BMGC_DS07992,BMG_DS029755,,,,,,,DOID:901,liver lymphoma,C1112746,,,MONDO:0004695,liver lymphoma,
+BMGC_DS07993,BMG_DS029756,,,,,,,,,C1112747,,,MONDO:0016671,sickle cell-hemoglobin E disease syndrome,
+BMGC_DS07994,BMG_DS029758,,,,,,,DOID:3637,childhood spinal cord tumor,C1134515,,,MONDO:0002716,childhood spinal cord tumor,
+BMGC_DS07995,BMG_DS029759,,,,,,,DOID:3008,invasive ductal carcinoma,C1134719,,,,,
+BMGC_DS07996,BMG_DS029761,,,,,,,DOID:11149,aqueous misdirection,C1135189,,,MONDO:0001206,aqueous misdirection,
+BMGC_DS07997,BMG_DS029762,,"Heart Failure, Systolic","Heart Failure, Systolic",,,,DOID:9651,systolic heart failure,C1135191,D054143,,MONDO:0006993,systolic heart failure,
+BMGC_DS07998,BMG_DS029764,,"Heart Failure, Diastolic","Heart Failure, Diastolic",,,,DOID:9775,diastolic heart failure,C1135196,D054144,,MONDO:0006727,diastolic heart failure,
+BMGC_DS07999,BMG_DS029768,,Dieulafoy lesion (hemorrhagic) of stomach and duodenum,,,,K31.82,DOID:12070,Dieulafoy lesion,C1135229,,,,,
+BMGC_DS08000,BMG_DS029779,,"Meningitis, Meningococcal, Serogroup A","Meningitis, Meningococcal",,,,DOID:0080176,meningococcal meningitis,C1135745,D008585,,,,
+BMGC_DS08001,BMG_DS029780,,"Meningitis, Meningococcal, Serogroup B","Meningitis, Meningococcal",,,,DOID:0080176,meningococcal meningitis,C1135746,D008585,,,,
+BMGC_DS08002,BMG_DS029781,,"Meningitis, Meningococcal, Serogroup C","Meningitis, Meningococcal",,,,DOID:0080176,meningococcal meningitis,C1135747,D008585,,,,
+BMGC_DS08003,BMG_DS029782,,"Acquired Metabolic Diseases, Nervous System","Brain Diseases, Metabolic",,,,,,C1135773,D001928,,,,
+BMGC_DS08004,BMG_DS029785,,,,,,,DOID:3590,gestational trophoblastic neoplasm,C1135868,,,MONDO:0018944,gestational trophoblastic neoplasm,
+BMGC_DS08005,BMG_DS029787,,,,,,,DOID:4320,non-gestational choriocarcinoma,C1135873,,,MONDO:0006871,non-gestational choriocarcinoma,
+BMGC_DS08006,BMG_DS029788,,"Wasting Disease, Chronic","Wasting Disease, Chronic",,,,DOID:3530,chronic wasting disease,C1135993,D034081,,MONDO:0002680,chronic wasting disease,
+BMGC_DS08007,BMG_DS029789,,,,,,,DOID:3663,cutaneous mastocytosis,C1136033,,154800,MONDO:0019023,cutaneous mastocytosis,
+BMGC_DS08008,BMG_DS029790,71390001,Plasma cell dyscrasia,,,,,DOID:6536,plasma cell neoplasm,C1136084,,MTHU071575,,,Plasma cell dyscrasia | Plasma cell dyscrasia (disorder)
+BMGC_DS08009,BMG_DS029792,,Water Stress,Dehydration,,,,,,C1136135,D003681,,,,
+BMGC_DS08010,BMG_DS029795,,"Meningitis, Meningococcal, Serogroup Y","Meningitis, Meningococcal",,,,DOID:0080176,meningococcal meningitis,C1136209,D008585,,,,
+BMGC_DS08011,BMG_DS029796,,"Meningitis, Meningococcal, Serogroup W-135","Meningitis, Meningococcal",,,,DOID:0080176,meningococcal meningitis,C1136210,D008585,,,,
+BMGC_DS08012,BMG_DS029797,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED",,,,,,,C1136249,,300427;300495,MONDO:0100284,X-linked intellectual disability,
+BMGC_DS08013,BMG_DS029798,,HIV-Associated Lipodystrophy Syndrome,HIV-Associated Lipodystrophy Syndrome,,,,,,C1136321,D039682,,,,
+BMGC_DS08014,BMG_DS029800,,Sclerocystic Ovaries,Polycystic Ovary Syndrome,,,,,,C1136382,D011085,,,,
+BMGC_DS08015,BMG_DS029801,,"Retinoschisis, Degenerative",Retinoschisis,,,,,,C1137478,D041441,,,,
+BMGC_DS08016,BMG_DS029803,,"Genetic Diseases, X-Linked","Genetic Diseases, X-Linked",,,,,,C1138434,D040181,,MONDO:0000425,X-linked disease,
+BMGC_DS08017,BMG_DS029804,,,,,,,DOID:2394,ovarian cancer,C1140680,,167000,MONDO:0008170,ovarian cancer,
+BMGC_DS08018,BMG_DS029805,442917000,Familial long QT syndrome,,,,,,,C1141890,,,MONDO:0019171,familial long QT syndrome,Congenital long QT syndrome | Inherited long QT syndrome | Familial long QT syndrome | Familial long QT syndrome (disorder)
+BMGC_DS08019,BMG_DS029806,129576003,Purple glove syndrome,,,,,,,C1141936,,,,,Purple glove syndrome | Purple glove syndrome (disorder)
+BMGC_DS08020,BMG_DS029811,421784001,Carnitine deficiency,,,,,,,C1142132,,,,,Carnitine deficiency (disorder) | Carnitine deficiency
+BMGC_DS08021,BMG_DS029813,,,,,,,DOID:0050451,Brugada syndrome,C1142166,,,MONDO:0015263,Brugada syndrome,
+BMGC_DS08022,BMG_DS029823,428763004,Bacteremia caused by Staphylococcus aureus,,,,,,,C1142423,,,,,Staphylococcus aureus bacteraemia | Staphylococcus aureus bacteremia | Bacteremia caused by Staphylococcus aureus | Bacteremia caused by Staphylococcus aureus (finding) | Bacteraemia caused by Staphylococcus aureus
+BMGC_DS08023,BMG_DS029830,,,,,,,,,C1145628,,,MONDO:0001292,autonomic nervous system disorder,
+BMGC_DS08024,BMG_DS029831,,Respiratory Failure,Respiratory Insufficiency,,,,,,C1145670,D012131,,MONDO:0021113,respiratory failure,
+BMGC_DS08025,BMG_DS029832,,Stomach Diverticulosis,"Diverticulosis, Stomach",,,,DOID:4370,stomach diverticulosis,C1148546,D045724,,MONDO:0002976,stomach diverticulosis,
+BMGC_DS08026,BMG_DS029833,,X-Linked Dyskeratosis Congenita,Dyskeratosis Congenita,,,,,,C1148551,D019871,305000,MONDO:0010584,"dyskeratosis congenita, X-linked",
+BMGC_DS08027,BMG_DS029834,,,,,,,DOID:2870,endometrial adenocarcinoma,C1153706,,,MONDO:0005461,endometrium adenocarcinoma,
+BMGC_DS08028,BMG_DS029835,,,,,,,DOID:5221,chronic polyneuropathy,C1167650,,,MONDO:0003335,chronic polyneuropathy,
+BMGC_DS08029,BMG_DS029838,,Pleuropericarditis,Pericarditis,,,,,,C1167732,D010493,,,,
+BMGC_DS08030,BMG_DS029840,129624009;404633004,Cogan-Reese syndrome,,,,,DOID:0060217,Cogan-Reese syndrome,C1168173,,,MONDO:0020370,Cogan-Reese syndrome,Nodular unilateral glaucoma | Cogan-Reese syndrome | Nodular unilateral glaucoma (disorder) | Cogan-Reese syndrome (disorder) | Cogan-Reese syndrome | Iris naevus syndrome | Iris nevus syndrome | Nodular unilateral glaucoma
+BMGC_DS08031,BMG_DS029842,,,,,,,,,C1168198,,,MONDO:0018955,recurrent respiratory papillomatosis,
+BMGC_DS08032,BMG_DS029843,,,,,,,DOID:3930,otitis interna,C1168225,,,MONDO:0002812,infectious otitis interna,
+BMGC_DS08033,BMG_DS029847,,,,,,,DOID:5520,head and neck squamous cell carcinoma,C1168401,,275355,MONDO:0010150,head and neck squamous cell carcinoma,
+BMGC_DS08034,BMG_DS029850,,Severe Acute Respiratory Syndrome,Severe Acute Respiratory Syndrome,,,,DOID:2945,severe acute respiratory syndrome,C1175175,D045169,,MONDO:0005091,severe acute respiratory syndrome,
+BMGC_DS08035,BMG_DS029851,,,,,,,DOID:3007,breast ductal carcinoma,C1176475,,,,,
+BMGC_DS08036,BMG_DS029853,,Child Malnutrition,Child Nutrition Disorders,,,,,,C1257753,D015362,,,,
+BMGC_DS08037,BMG_DS029854,302872003,Overnutrition,Overnutrition,,,,DOID:654,overnutrition,C1257763,D044343,,MONDO:0003916,overnutrition,Disorder of hyperalimentation | Overfed | Overnutrition | Disorder of hyperalimentation (disorder)
+BMGC_DS08038,BMG_DS029855,,Child Overnutrition,Child Nutrition Disorders,,,,,,C1257764,D015362,,,,
+BMGC_DS08039,BMG_DS029856,,Infant Overnutrition,Infant Nutrition Disorders,,,,,,C1257765,D007228,,,,
+BMGC_DS08040,BMG_DS029857,,"Steroid Metabolism, Inborn Errors","Steroid Metabolism, Inborn Errors",,,,DOID:1701,steroid inherited metabolic disorder,C1257809,D043202,,MONDO:0005523,steroid inherited metabolic disorder,
+BMGC_DS08041,BMG_DS029858,,,,,,,DOID:0060185,Clostridium difficile colitis,C1257843,,,,,
+BMGC_DS08042,BMG_DS029859,,Clostridium Enterocolitis,"Enterocolitis, Pseudomembranous",,,,DOID:0060185,Clostridium difficile colitis,C1257844,D004761,,,,
+BMGC_DS08043,BMG_DS029860,,"Enteritis, Pseudomembranous","Enterocolitis, Pseudomembranous",,,,DOID:0060185,Clostridium difficile colitis,C1257845,D004761,,,,
+BMGC_DS08044,BMG_DS029867,,,,,,,,,C1257877,,,MONDO:0000550,extra-adrenal sympathetic paraganglioma,
+BMGC_DS08045,BMG_DS029869,,Intestinal Polyposis,Intestinal Polyposis,,,,,,C1257915,D044483,,MONDO:0024292,gastrointestinal polyp,
+BMGC_DS08046,BMG_DS029870,,Glucose Metabolism Disorders,Glucose Metabolism Disorders,,,,DOID:4194,glucose metabolism disease,C1257958,D044882,,MONDO:0002908,glucose metabolism disease,
+BMGC_DS08047,BMG_DS029872,,Endogenous Hyperinsulinism,Hyperinsulinism,,,,,,C1257963,D006946,,,,
+BMGC_DS08048,BMG_DS029873,,Exogenous Hyperinsulinism,Hyperinsulinism,,,,,,C1257964,D006946,,,,
+BMGC_DS08049,BMG_DS029874,,Compensatory Hyperinsulinemia,Hyperinsulinism,,,,,,C1257965,D006946,,,,
+BMGC_DS08050,BMG_DS029878,,Barrett Epithelium,Barrett Esophagus,,,,,,C1258085,D001471,,,,
+BMGC_DS08051,BMG_DS029880,,Diffuse Scleroderma,"Scleroderma, Diffuse",,,,DOID:1580,diffuse scleroderma,C1258104,D045743,,MONDO:0005019,diffuse scleroderma,
+BMGC_DS08052,BMG_DS029881,278524008;81060008,Ileus,Ileus,,,,DOID:8440,ileus,C1258215,D045823,MTHU007815,MONDO:0004567,ileus,Ileus | Ileus (disorder) | Intestinal obstruction | Bowel obstruction | Obstruction of intestine | IO - Intestinal obstruction | Intestinal obstruction (disorder)
+BMGC_DS08053,BMG_DS029889,,Moraxellaceae Infections,Moraxellaceae Infections,,,,,,C1258225,D045828,,MONDO:0006878,Moraxellaceae infectious disease,
+BMGC_DS08054,BMG_DS029890,,Psychobacter Infections,Moraxellaceae Infections,,,,,,C1258226,D045828,,MONDO:0006878,Moraxellaceae infectious disease,
+BMGC_DS08055,BMG_DS029891,,,,,,,DOID:6262,follicular dendritic cell sarcoma,C1260325,,,MONDO:0005764,follicular dendritic cell sarcoma,
+BMGC_DS08056,BMG_DS029892,,,,,,,DOID:7848,interdigitating dendritic cell sarcoma,C1260326,,,MONDO:0005813,interdigitating dendritic cell sarcoma,
+BMGC_DS08057,BMG_DS029893,,,,,,,DOID:7146,Langerhans cell sarcoma,C1260327,,,MONDO:0019480,Langerhans cell sarcoma,
+BMGC_DS08058,BMG_DS029898,,,,,,,DOID:11786,splenic sequestration,C1260402,,,MONDO:0001366,splenic sequestration,
+BMGC_DS08059,BMG_DS029899,,,,,,,DOID:437,myasthenia gravis,C1260409,,,,,
+BMGC_DS08060,BMG_DS029905,8722008,Aortic valve disorder,,,,,DOID:62,aortic valve disease,C1260873,,,MONDO:0003803,aortic valve disorder,Aortic valve disorder | Aortic valve disorder (disorder) | Aortic valve disease | AVD - Aortic valve disease
+BMGC_DS08061,BMG_DS029920,,"Anemia, Diamond-Blackfan","Anemia, Diamond-Blackfan",,,,DOID:1339,Diamond-Blackfan anemia,C1260899,D029503,,MONDO:0015253,Diamond-Blackfan anemia,
+BMGC_DS08062,BMG_DS029923,111589005,Dysfibrinogenemia,,,,,,,C1260903,,,,,Dysfibrinogenemia | Dysfibrinogenaemia | Dysfibrinogenemia (disorder)
+BMGC_DS08063,BMG_DS029925,197718007;9772004,Infection by Pasteurella multocida,,,,,,,C1260911,,,MONDO:0040998,Pasteurella multocida infectious disease,Infection by Pasteurella multocida | Infection caused by Pasteurella multocida | Infection caused by Pasteurella multocida (disorder) | Hemorrhagic septicemia due to Pasteurella multocida | Haemorrhagic septicaemia due to Pasteurella multocida | Hemorrhagic septicemia due to Pasteurella multocida (disorder)
+BMGC_DS08064,BMG_DS029928,186903006,Late latent syphilis,,,,,,,C1260915,,,MONDO:0040923,late latent syphilis,Late latent syphilis | Late latent syphilis (disorder)
+BMGC_DS08065,BMG_DS029929,195888009,Proteus pneumonia,,,,,,,C1260917,,,,,Proteus pneumonia | Proteus pneumonia (disorder)
+BMGC_DS08066,BMG_DS029934,,,,,,,DOID:5570,malignant acrospiroma,C1260964,,,MONDO:0024245,ductal eccrine adenocarcinoma,
+BMGC_DS08067,BMG_DS029935,,,,,,,,,C1260965,,,MONDO:0016611,lipoblastoma,
+BMGC_DS08068,BMG_DS029941,,Progeria short stature pigmented nevi,,,,,,,C1261128,C536422,176690,MONDO:0008311,progeria-short stature-pigmented nevi syndrome,
+BMGC_DS08069,BMG_DS029945,373666002,Pontoneocerebellar hypoplasia,,,,,,,C1261175,,,MONDO:0020135,pontocerebellar hypoplasia,Pontoneocerebellar hypoplasia (disorder) | Pontoneocerebellar hypoplasia
+BMGC_DS08070,BMG_DS029949,270550006,Pelvic inflammatory disease caused by Metamycoplasma hominis,,,,,,,C1261256,,,,,Pelvic inflammatory disease caused by Mycoplasma hominis | Pelvic inflammatory disease caused by Metamycoplasma hominis | Pelvic inflammatory disease caused by Metamycoplasma hominis (disorder)
+BMGC_DS08071,BMG_DS029952,155885003;266562000;197843007;266629000;74445007,Trigonitis,,GC00.0,Trigonitis,N30.3,DOID:13507,trigonitis,C1261278,,,MONDO:0001732,trigonitis,(Cystitis NOS) or (trigonitis) | Trigonitis | Cystitis NOS | (Cystitis NOS) or (trigonitis) (disorder) | Trigonitis | Trigonitis (disorder) | (Trigonitis) or (follicular cystitis) | Follicular cystitis | Trigonitis | (Trigonitis) or (follicular cystitis) (disorder) | (Cystitis NOS) or (trigonitis) | Cystitis NOS | Trigonitis | (Cystitis NOS) or (trigonitis) (disorder)
+BMGC_DS08072,BMG_DS029954,82684004;187089001,Actinomycetoma,Mycetoma,1C43,Actinomycetoma,B47.1,,,C1261283,D008271,,,,Actinomycotic madura foot | Actinomycotic maduromycosis | Actinomycotic mycetoma | Actinomycotic schizomycetoma | Actinomycetoma | Actinomycotic madura foot (disorder) | Actinomycetoma | Actinomycotic mycetoma | Actinomycotic mycetoma (disorder) | Actinomycotic mycetema
+BMGC_DS08073,BMG_DS029956,193388002;267612009,"Degeneration of macula due to cyst, hole or pseudohole",,,,,DOID:13214,hole retinal cyst,C1261331,,,MONDO:0001663,hole retinal cyst,"Degeneration of macula due to cyst, hole or pseudohole | Macular cyst or hole | Degeneration of macular due to cyst, hole or pseudohole | Macular hole | Degeneration of macular due to cyst &/or hole &/or pseudohole | Degeneration of macular due to cyst &/or hole &/or pseudohole (disorder) | Degeneration of macula due to cyst, hole or pseudohole | Degeneration of macula due to cyst, hole or pseudohole (disorder)"
+BMGC_DS08074,BMG_DS029964,,,,,,,,,C1261473,,,MONDO:0005089,sarcoma,
+BMGC_DS08075,BMG_DS029967,703470001,Bacterial sinusitis,,,,,,,C1262006,,,,,Bacterial sinusitis | Bacterial sinusitis (disorder)
+BMGC_DS08076,BMG_DS029970,314558005,Fungal keratitis,,,,,,,C1262117,,,MONDO:0033821,fungal keratitis,Fungal keratitis | Fungal keratitis (disorder) | Mycotic keratitis | Fungal infection of cornea | Keratomycosis
+BMGC_DS08077,BMG_DS029977,32183007;359804008,Eosinophilic gastroenteritis,,,,,DOID:4031,eosinophilic gastroenteritis,C1262481,C535952,,MONDO:0016129,eosinophilic gastroenteritis,Infection by Anisakis larva | Infection by Anisakis larva (disorder) | Eosinophilic gastroenteritis | Eosinophilic gastroenteritis (disorder)
+BMGC_DS08078,BMG_DS029982,,"Hepatitis, Drug-Induced",Chemical and Drug Induced Liver Injury,,,,,,C1262760,D056486,,MONDO:0002184,drug-induced hepatitis,
+BMGC_DS08079,BMG_DS030019,123609007,Subacute glomerulonephritis,,,,,DOID:4782,subacute glomerulonephritis,C1263744,,,MONDO:0003138,subacute glomerulonephritis,Subacute glomerulonephritis | Subacute glomerulonephritis (disorder)
+BMGC_DS08080,BMG_DS030030,125585007,Female genital tract infection,,,,,,,C1263758,,,,,Female genital tract infection | Female genital tract infection (disorder)
+BMGC_DS08081,BMG_DS030051,,,,,,,,,C1263846,,,MONDO:0007743,attention deficit-hyperactivity disorder,
+BMGC_DS08082,BMG_DS030060,128208007,Peripheral axonal neuropathy,,,,,,,C1263857,,MTHU001038,MONDO:0004183,axonal neuropathy,Peripheral axonal neuropathy | Peripheral axonal neuropathy (disorder)
+BMGC_DS08083,BMG_DS030061,,"Muscular dystrophy congenital, merosin negative",,,,,DOID:0110636,congenital merosin-deficient muscular dystrophy 1A,C1263858,C537384,607855,MONDO:0011925,congenital merosin-deficient muscular dystrophy 1A,
+BMGC_DS08084,BMG_DS030079,,,,,,,DOID:368,cerebrum cancer,C1263885,,,MONDO:0021374,neoplasm of cerebral hemisphere,
+BMGC_DS08085,BMG_DS030080,,,,,,,DOID:12016,frontal lobe neoplasm,C1263886,,,MONDO:0001421,frontal lobe neoplasm,
+BMGC_DS08086,BMG_DS030081,,,,,,,DOID:2135,temporal lobe neoplasm,C1263887,,,MONDO:0021372,neoplasm of temporal lobe,
+BMGC_DS08087,BMG_DS030082,,,,,,,DOID:14384,parietal lobe neoplasm,C1263888,,,MONDO:0021373,neoplasm of parietal lobe,
+BMGC_DS08088,BMG_DS030083,,,,,,,DOID:910,occipital lobe neoplasm,C1263889,,,MONDO:0004709,occipital lobe neoplasm,
+BMGC_DS08089,BMG_DS030084,,,,,,,DOID:4847,cauda equina neoplasm,C1263892,,,MONDO:0003164,cauda equina neoplasm,
+BMGC_DS08090,BMG_DS030085,,,,,,,DOID:2817,cranial nerve III tumor,C1263895,,,MONDO:0002435,oculomotor nerve neoplasm,
+BMGC_DS08091,BMG_DS030086,,,,,,,DOID:3421,trochlear nerve neoplasm,C1263896,,,MONDO:0002642,trochlear nerve neoplasm,
+BMGC_DS08092,BMG_DS030087,,,,,,,DOID:1201,trigeminal nerve neoplasm,C1263897,,,MONDO:0001420,trigeminal nerve neoplasm,
+BMGC_DS08093,BMG_DS030088,,,,,,,DOID:14125,abducens nerve neoplasm,C1263898,,,MONDO:0001884,abducens nerve neoplasm,
+BMGC_DS08094,BMG_DS030089,,,,,,,DOID:1760,facial nerve neoplasm,C1263899,,,MONDO:0002101,facial nerve neoplasm,
+BMGC_DS08095,BMG_DS030090,,,,,,,DOID:3417,glossopharyngeal nerve neoplasm,C1263900,,,MONDO:0002638,glossopharyngeal nerve neoplasm,
+BMGC_DS08096,BMG_DS030091,,,,,,,DOID:12984,vagus nerve neoplasm,C1263901,,,MONDO:0001608,vagus nerve neoplasm,
+BMGC_DS08097,BMG_DS030092,,,,,,,DOID:337,spinal accessory nerve neoplasm,C1263902,,,MONDO:0002626,spinal accessory nerve neoplasm,
+BMGC_DS08098,BMG_DS030093,,,,,,,DOID:3198,hypoglossal nerve neoplasm,C1263903,,,MONDO:0002550,hypoglossal nerve neoplasm,
+BMGC_DS08099,BMG_DS030125,127048005,Sickle cell-Hemoglobin O Arab disease,,,,,,,C1264000,,,,,Sickle cell-Hemoglobin O Arab disease | Sickle cell-Haemoglobin O Arab disease | Sickle cell-Hemoglobin O Arab disease (disorder)
+BMGC_DS08100,BMG_DS030155,,"von Willebrand Disease, Type 1","von Willebrand Disease, Type 1",,,,DOID:0060573,von Willebrand's disease 1,C1264039,D056725,193400,MONDO:0008668,von Willebrand disease 1,
+BMGC_DS08101,BMG_DS030156,,"von Willebrand Disease, Type 2","von Willebrand Disease, Type 2",,,,DOID:0060574,von Willebrand's disease 2,C1264040,D056728,613554,MONDO:0013304,von Willebrand disease 2,
+BMGC_DS08102,BMG_DS030157,,"von Willebrand Disease, Type 3","von Willebrand Disease, Type 3",,,,DOID:0111054,von Willebrand's disease 3,C1264041,D056729,277480,MONDO:0010191,von Willebrand disease 3,
+BMGC_DS08103,BMG_DS030204,,,,,,,DOID:6658,pulmonary large cell neuroendocrine carcinoma,C1265996,,,MONDO:0005057,large cell neuroendocrine carcinoma,
+BMGC_DS08104,BMG_DS030205,,,,,,,DOID:7480,large cell carcinoma with rhabdoid phenotype,C1265997,,,MONDO:0004237,large cell carcinoma with rhabdoid phenotype,
+BMGC_DS08105,BMG_DS030206,,,,,,,DOID:5522,basaloid squamous cell carcinoma,C1266005,,,MONDO:0003486,basaloid squamous cell carcinoma,
+BMGC_DS08106,BMG_DS030207,,,,,,,DOID:6239,non-invasive bladder papillary urothelial neoplasm,C1266010,,,,,
+BMGC_DS08107,BMG_DS030208,,,,,,,DOID:5026,sclerosing hepatic carcinoma,C1266018,,,MONDO:0003246,sclerosing hepatic carcinoma,
+BMGC_DS08108,BMG_DS030209,,,,,,,DOID:5016,hepatocellular clear cell carcinoma,C1266020,,,MONDO:0003243,hepatocellular clear cell carcinoma,
+BMGC_DS08109,BMG_DS030210,,,,,,,DOID:7539,pregnancy adenoma,C1266023,,,MONDO:0004271,pregnancy adenoma,
+BMGC_DS08110,BMG_DS030211,,,,,,,DOID:7531,anal gland adenocarcinoma,C1266027,,,MONDO:0004266,anal gland adenocarcinoma,
+BMGC_DS08111,BMG_DS030215,,,,,,,DOID:5468,biliary papillomatosis,C1266038,,,,,
+BMGC_DS08112,BMG_DS030216,,,,,,,DOID:4471,chromophobe renal cell carcinoma,C1266042,,,MONDO:0017885,chromophobe renal cell carcinoma,
+BMGC_DS08113,BMG_DS030217,,,,,,,DOID:4473,sarcomatoid renal cell carcinoma,C1266043,,,MONDO:0003012,sarcomatoid renal cell carcinoma,
+BMGC_DS08114,BMG_DS030218,,,,,,,DOID:4464,collecting duct carcinoma,C1266044,,,MONDO:0005220,collecting duct carcinoma,
+BMGC_DS08115,BMG_DS030219,,,,,,,DOID:6404,metanephric adenoma,C1266045,,,MONDO:0006301,metanephric adenoma,
+BMGC_DS08116,BMG_DS030220,,,,,,,DOID:8292,atypical follicular adenoma,C1266046,,,MONDO:0004524,thyroid gland atypical follicular adenoma,
+BMGC_DS08117,BMG_DS030222,,,,,,,DOID:7289,"endometrial endometrioid adenocarcinoma, secretory variant",C1266057,,,MONDO:0004174,secretory uterine corpus endometrioid adenocarcinoma,
+BMGC_DS08118,BMG_DS030224,,,,,,,DOID:7960,malignant spiradenoma,C1266063,,,MONDO:0004412,malignant spiradenoma,
+BMGC_DS08119,BMG_DS030225,,,,,,,DOID:7566,eccrine porocarcinoma,C1266065,,,MONDO:0006189,eccrine porocarcinoma,
+BMGC_DS08120,BMG_DS030226,,,,,,,DOID:4920,eccrine adenocarcinoma,C1266066,,,,,
+BMGC_DS08121,BMG_DS030227,,,,,,,DOID:7575,pancreatic intraductal papillary-mucinous neoplasm,C1266071,,,,,
+BMGC_DS08122,BMG_DS030228,,,,,,,DOID:7237,pancreatic non-invasive mucinous cystadenocarcinoma,C1266078,,,MONDO:0004159,pancreatic non-invasive mucinous cystadenocarcinoma,
+BMGC_DS08123,BMG_DS030229,,,,,,,DOID:8340,endocervical type cervical mucinous adenocarcinoma,C1266079,,,,,
+BMGC_DS08124,BMG_DS030230,,,,,,,DOID:7729,acinar cell cystadenocarcinoma,C1266087,,,MONDO:0004343,pancreatic acinar cell cystadenocarcinoma,
+BMGC_DS08125,BMG_DS030232,,,,,,,DOID:3279,spindle cell thymoma,C1266091,,,MONDO:0002588,thymoma type A,
+BMGC_DS08126,BMG_DS030233,,,,,,,DOID:3280,mixed type thymoma,C1266092,,,MONDO:0016975,thymoma type AB,
+BMGC_DS08127,BMG_DS030234,,,,,,,DOID:6723,malignant type AB thymoma,C1266093,,,MONDO:0003976,malignant type AB thymoma,
+BMGC_DS08128,BMG_DS030235,,,,,,,DOID:6917,predominantly cortical thymoma,C1266094,,,MONDO:0006459,thymoma type B1,
+BMGC_DS08129,BMG_DS030236,,,,,,,DOID:6530,thymoma type B2,C1266095,,,MONDO:0003915,cortical thymoma,
+BMGC_DS08130,BMG_DS030238,,,,,,,,,C1266101,,,MONDO:0018079,thymic epithelial neoplasm,
+BMGC_DS08131,BMG_DS030239,,,,,,,DOID:5233,glomangiosarcoma,C1266111,,,MONDO:0003340,malignant glomus tumor,
+BMGC_DS08132,BMG_DS030240,,,,,,,DOID:6379,diffuse meningeal melanocytosis,C1266112,,,MONDO:0003867,diffuse meningeal melanocytosis,
+BMGC_DS08133,BMG_DS030242,,,,,,,DOID:8243,meningeal melanomatosis,C1266114,,,MONDO:0004512,meningeal melanomatosis,
+BMGC_DS08134,BMG_DS030243,,,,,,,,,C1266119,,,MONDO:0016238,solitary fibrous tumor,
+BMGC_DS08135,BMG_DS030244,,,,,,,DOID:4386,myofibroma,C1266121,,,MONDO:0006312,myofibroma,
+BMGC_DS08136,BMG_DS030246,,,,,,,,,C1266127,,612160,MONDO:0012809,"histiocytoma, Angiomatoid fibrous",
+BMGC_DS08137,BMG_DS030247,,,,,,,DOID:2685,ossifying fibromyxoid tumor,C1266128,,,MONDO:0006330,ossifying fibromyxoid tumor,
+BMGC_DS08138,BMG_DS030249,,,,,,,DOID:5698,fibroblastic liposarcoma,C1266130,,,MONDO:0003590,fibroblastic liposarcoma,
+BMGC_DS08139,BMG_DS030250,,,,,,,DOID:10208,chondroid lipoma,C1266131,,,MONDO:0000977,chondroid lipoma,
+BMGC_DS08140,BMG_DS030251,,,,,,,DOID:3260,spindle cell rhabdomyosarcoma,C1266134,,,MONDO:0002581,spindle cell rhabdomyosarcoma,
+BMGC_DS08141,BMG_DS030254,,,,,,,DOID:2698,nephrogenic adenofibroma,C1266141,,,MONDO:0002396,nephrogenic adenofibroma,
+BMGC_DS08142,BMG_DS030255,,,,,,,DOID:4769,pleuropulmonary blastoma,C1266144,,601200,MONDO:0011014,pleuropulmonary blastoma,
+BMGC_DS08143,BMG_DS030257,,,,,,,DOID:3593,epithelioid trophoblastic tumor,C1266159,,,MONDO:0016787,epithelioid trophoblastic tumor,
+BMGC_DS08144,BMG_DS030258,,,,,,,,,C1266165,,,MONDO:0006246,high grade surface osteosarcoma,
+BMGC_DS08145,BMG_DS030259,,,,,,,DOID:7602,conventional osteosarcoma,C1266166,,,,,
+BMGC_DS08146,BMG_DS030260,,,,,,,DOID:5867,clear cell chondrosarcoma,C1266167,,,MONDO:0003684,clear cell chondrosarcoma,
+BMGC_DS08147,BMG_DS030261,,,,,,,DOID:2704,malignant giant cell tumor of the tendon sheath,C1266168,,,MONDO:0002401,malignant tenosynovial giant cell tumor,
+BMGC_DS08148,BMG_DS030262,,,,,,,DOID:4152,chondroid chordoma,C1266173,,,MONDO:0006145,chondroid chordoma,
+BMGC_DS08149,BMG_DS030263,,,,,,,DOID:2647,parachordoma,C1266175,,,MONDO:0006351,parachordoma,
+BMGC_DS08150,BMG_DS030265,,,,,,,DOID:2679,dysembryoplastic neuroepithelial tumor,C1266177,,,MONDO:0005505,dysembryoplastic neuroepithelial tumor,
+BMGC_DS08151,BMG_DS030266,,,,,,,DOID:4856,gliofibroma,C1266178,,,MONDO:0003170,gliofibroma,
+BMGC_DS08152,BMG_DS030267,,,,,,,DOID:3857,large cell medulloblastoma,C1266180,,,MONDO:0002791,large cell medulloblastoma,
+BMGC_DS08153,BMG_DS030268,,,,,,,DOID:2129,atypical teratoid rhabdoid tumor,C1266184,,,MONDO:0020560,atypical teratoid rhabdoid tumor,
+BMGC_DS08154,BMG_DS030269,,,,,,,,,C1266188,,,MONDO:0016751,malignant perineurioma,
+BMGC_DS08155,BMG_DS030270,,,,,,,DOID:8543,"Hodgkin's lymphoma, lymphocytic-histiocytic predominance",C1266194,,,MONDO:0004604,"Hodgkin's lymphoma, lymphocytic-histiocytic predominance",
+BMGC_DS08156,BMG_DS030289,,Congenital Thrombotic Thrombocytopenic Purpura,"Purpura, Thrombotic Thrombocytopenic",,,,,,C1268935,D011697,274150,MONDO:0010122,congenital thrombotic thrombocytopenic purpura,
+BMGC_DS08157,BMG_DS030293,,,,,,,,,C1269683,,608516,MONDO:0002009,major depressive disorder,
+BMGC_DS08158,BMG_DS030317,,,,,,,,,C1271219,,129750,MONDO:0007515,ectopia pupillae,
+BMGC_DS08159,BMG_DS030318,392133001,Pigment dispersion syndrome (disorder),,,,,,,C1271398,,600510,MONDO:0010896,pigment dispersion syndrome,Pigment dispersion syndrome (disorder) | Pigment dispersion syndrome
+BMGC_DS08160,BMG_DS030347,,,,,,,DOID:6322,tibial adamantinoma,C1273017,,,MONDO:0006469,tibial adamantinoma,
+BMGC_DS08161,BMG_DS030348,395650008;395704004,Left ventricular diastolic dysfunction,,,,,,,C1273070,,MTHU076255,,,Left ventricular diastolic dysfunction | Left ventricular diastolic dysfunction (disorder) | Left ventricular diastolic dysfunction (disorder) | Left ventricular diastolic dysfunction
+BMGC_DS08162,BMG_DS030354,372936000,Infection due to Penicillium marneffei (disorder),,,,,,,C1274008,,,MONDO:0000304,penicilliosis,Infection caused by Penicillium marneffei | Infection caused by Talaromyces marneffei | Infection caused by Talaromyces marneffei (disorder)
+BMGC_DS08163,BMG_DS030376,402717008,IgA pemphigus,,,,,DOID:0080851,IgA pemphigus,C1274167,,,MONDO:0034127,IgA pemphigus,IgA pemphigus | Immunoglobulin A pemphigus (disorder) | Immunoglobulin A pemphigus
+BMGC_DS08164,BMG_DS030392,402736003,Factitious skin disease,,,,,DOID:9165,neurotic excoriation,C1274184,,,MONDO:0006586,neurotic excoriation,Factitious skin disease (disorder) | Factitious skin disease
+BMGC_DS08165,BMG_DS030404,,,,,,,,,C1274215,,,MONDO:0017265,autosomal recessive congenital ichthyosis,
+BMGC_DS08166,BMG_DS030405,,,,,,,DOID:0060361,punctate palmoplantar keratoderma,C1274216,,,,,
+BMGC_DS08167,BMG_DS030413,402786009,Chylomicronemia syndrome,,,,,,,C1274228,,,,,Chylomicronemia syndrome (disorder) | Chylomicronemia syndrome
+BMGC_DS08168,BMG_DS030417,402792003,T-lymphocyte immunodeficiency,,,,,DOID:11200,T cell deficiency,C1274233,,,MONDO:0003780,T-cell immunodeficiency,T-lymphocyte immunodeficiency (disorder) | T-lymphocyte immunodeficiency
+BMGC_DS08169,BMG_DS030474,402892009,Recurrent herpes simplex labialis,,,,,,,C1274321,,,,,Recurrent herpes simplex labialis (disorder) | Recurrent herpes simplex labialis | Recurrent herpes labialis
+BMGC_DS08170,BMG_DS030476,402894005,Recurrent genital herpes simplex,,,,,,,C1274323,,,,,Recurrent genital herpes simplex (disorder) | Recurrent genital herpes simplex | Recurrent herpes genitalis
+BMGC_DS08171,BMG_DS030506,402937004,Streptococcal infection of skin,,,,,,,C1274355,,,,,Streptococcal infection of skin (disorder) | Streptococcal infection of skin
+BMGC_DS08172,BMG_DS030548,,Primary Cutaneous Nocardiosis,Nocardia Infections,,,,,,C1274400,D009617,,,,
+BMGC_DS08173,BMG_DS030613,403059006,Onychomycosis of toenails,,,,,,,C1274470,,,,,Onychomycosis of toenails (disorder) | Onychomycosis of toenails
+BMGC_DS08174,BMG_DS030691,403152000,Demodectic blepharitis,,,,,,,C1274557,,,,,Demodectic blepharitis (disorder) | Demodectic blepharitis
+BMGC_DS08175,BMG_DS030774,109441000119102,Central centrifugal cicatricial alopecia,,,,L66.81,,,C1274708,,618352,MONDO:0022113,central centrifugal cicatricial alopecia,Central centrifugal cicatricial alopecia (disorder) | Central centrifugal cicatricial alopecia | Hot comb alopecia
+BMGC_DS08176,BMG_DS030799,,Hyperhidrosis Palmaris Et Plantaris,,,,,,,C1274743,C563185,144110,MONDO:0007754,hyperhidrosis palmaris ET plantaris,
+BMGC_DS08177,BMG_DS030839,403435005,Ligneous conjunctivitis,,,,H10.51,,,C1274789,,MTHU023531,MONDO:0100560,ligneous conjunctivitis,Ligneous conjunctivitis (disorder) | Ligneous conjunctivitis
+BMGC_DS08178,BMG_DS030845,,,,,,,,,C1274795,,158310,MONDO:0008017,hereditary mucoepithelial dysplasia,
+BMGC_DS08179,BMG_DS030870,403488004,Systemic lupus erythematosus of childhood,,,,,,,C1274834,,,MONDO:0019725,pediatric systemic lupus erythematosus,Systemic lupus erythematosus of childhood (disorder) | Systemic lupus erythematosus of childhood
+BMGC_DS08180,BMG_DS030923,,Drug-Induced Stevens Johnson Syndrome,Stevens-Johnson Syndrome,,,,,,C1274933,D013262,,,,
+BMGC_DS08181,BMG_DS030972,403666006,Drug-induced mucositis,,,,,,,C1274988,,,,,Drug-induced mucositis (disorder) | Drug-induced mucositis
+BMGC_DS08182,BMG_DS031016,403767009,Acrocephalopolysyndactyly type 2,,,,,DOID:0060234,Carpenter syndrome,C1275078,,,MONDO:0019012,Carpenter syndrome,Acrocephalopolysyndactyly type II (disorder) | Acrocephalopolysyndactyly type II | Carpenter syndrome | Acrocephalopolysyndactyly type 2
+BMGC_DS08183,BMG_DS031017,,Sakati syndrome,,,,,DOID:0060359,Sakati-Nyhan syndrome,C1275079,C537227,101120,MONDO:0007040,Sakati-Nyhan syndrome,
+BMGC_DS08184,BMG_DS031018,403770008,Cardio-facio-cutaneous syndrome,,,,,,,C1275081,,,MONDO:0015280,cardiofaciocutaneous syndrome,Cardio-facio-cutaneous syndrome (disorder) | Cardio-facio-cutaneous syndrome
+BMGC_DS08185,BMG_DS031020,,,,,,,,,C1275084,,106070,MONDO:0007116,hereditary neurocutaneous angioma,
+BMGC_DS08186,BMG_DS031023,,Dykes Markes Harper syndrome,,,,,,,C1275088,C535727,242520,MONDO:0009445,ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome,
+BMGC_DS08187,BMG_DS031024,,"Ichthyosiform erythroderma, corneal involvement, deafness",,,,,,,C1275089,C537363,242150,MONDO:0009440,"ichthyosiform erythroderma, corneal involvement, and hearing loss",
+BMGC_DS08188,BMG_DS031038,403794008,Autosomal dominant familial wooly hair,,,,,,,C1275103,,,,,Autosomal dominant familial woolly hair | Autosomal dominant familial wooly hair (disorder) | Autosomal dominant familial wooly hair
+BMGC_DS08189,BMG_DS031046,403809003,Dystrophic epidermolysis bullosa inverse type,,,,,,,C1275113,,,MONDO:0019310,recessive dystrophic epidermolysis bullosa inversa,Dystrophic epidermolysis bullosa inverse type (disorder) | Dystrophic epidermolysis bullosa inverse type
+BMGC_DS08190,BMG_DS031047,,Epidermolysis Bullosa Pruriginosa,,,,,,,C1275114,C563192,604129,MONDO:0011398,dystrophic epidermolysis bullosa pruriginosa,
+BMGC_DS08191,BMG_DS031049,403812000,Autosomal recessive pseudoxanthoma elasticum,,,,,,,C1275116,,264800,MONDO:0009925,autosomal recessive inherited pseudoxanthoma elasticum,Autosomal recessive pseudoxanthoma elasticum (disorder) | Autosomal recessive pseudoxanthoma elasticum
+BMGC_DS08192,BMG_DS031051,,,,,,,,,C1275122,,,MONDO:0011114,familial multiple trichoepithelioma,
+BMGC_DS08193,BMG_DS031054,403833009,TNF receptor-associated periodic fever syndrome (TRAPS),,,,,,,C1275126,,142680,MONDO:0007727,autosomal dominant familial periodic fever,TNF receptor-associated periodic fever syndrome (TRAPS) | Familial autosomal dominant periodic fever | TNF receptor-associated periodic fever syndrome | TRAPS - TNF receptor-associated periodic fever syndrome | Tumor necrosis factor (TNF) receptor-associated periodic fever syndrome | Tumour necrosis factor (TNF) receptor-associated periodic fever syndrome | Tumor necrosis factor receptor-associated periodic fever syndrome | Tumor necrosis factor receptor-associated periodic fever syndrome (disorder) | Tumour necrosis factor receptor-associated periodic fever syndrome
+BMGC_DS08194,BMG_DS031071,,,,,,,DOID:2097,vulval Paget's disease,C1275217,,,MONDO:0002207,vulval Paget disease,
+BMGC_DS08195,BMG_DS031072,,,,,,,DOID:2435,skin glomangioma,C1275226,,,MONDO:0002298,cutaneous glomangioma,
+BMGC_DS08196,BMG_DS031078,,,,,,,DOID:1906,malignant skin fibrous histiocytoma,C1275254,,,MONDO:0002141,cutaneous undifferentiated pleomorphic sarcoma,
+BMGC_DS08197,BMG_DS031080,,,,,,,DOID:5149,epithelioid neurofibroma,C1275264,,,MONDO:0003302,epithelioid neurofibroma,
+BMGC_DS08198,BMG_DS031081,,Familial Multiple Lipomatosis,Familial Multiple Lipomatosis,,,,DOID:0070518,familial multiple lipomatosis,C1275273,D000071070,151900,MONDO:0007909,familial multiple lipomatosis,
+BMGC_DS08199,BMG_DS031082,,,,,,,DOID:5705,spindle cell liposarcoma,C1275275,,,MONDO:0003596,spindle cell liposarcoma,
+BMGC_DS08200,BMG_DS031084,,,,,,,DOID:4549,extraskeletal myxoid chondrosarcoma,C1275278,,612237,MONDO:0012825,extraskeletal myxoid chondrosarcoma,
+BMGC_DS08201,BMG_DS031085,,,,,,,DOID:4548,extraskeletal mesenchymal chondrosarcoma,C1275279,,,,,
+BMGC_DS08202,BMG_DS031134,396343006,Funisitis (disorder),,,,,,,C1275592,,,MONDO:0000410,funisitis,Funisitis (disorder) | Funisitis | Inflammation of umbilical cord
+BMGC_DS08203,BMG_DS031135,,,,,,,DOID:3868,melanotic medulloblastoma,C1275668,,,MONDO:0002796,melanotic medulloblastoma,
+BMGC_DS08204,BMG_DS031136,397549002,Meibomian gland dysfunction,,,,,,,C1275684,,MTHU045781,,,Meibomian gland dysfunction (disorder) | Meibomian gland dysfunction | Posterior blepharitis | MGD-Meibomian gland dysfunction
+BMGC_DS08205,BMG_DS031137,397568004,Avellino corneal dystrophy,,,,,DOID:0060444,granular corneal dystrophy 2,C1275685,C535474,607541,MONDO:0011855,granular corneal dystrophy type II,Avellino corneal dystrophy | Granular-lattice corneal dystrophy | Granular corneal dystrophy type II | Granular corneal dystrophy type II (disorder)
+BMGC_DS08206,BMG_DS031139,397573005,Herpes zoster keratitis,,,,,,,C1275687,,,,,Herpes zoster keratitis (disorder) | Herpes zoster keratitis | HZV (herpes zoster virus) keratitis
+BMGC_DS08207,BMG_DS031143,399040002;361207008,Congenital central hypoventilation,,,,,,,C1275808,,,MONDO:0800031,"central hypoventilation syndrome, congenital",CCHS - Congenital central hypoventilation | Congenital pulmonary hypoventilation | Congenital central hypoventilation | Congenital central hypoventilation (disorder) | Ondine curse | CCHS - Congenital central hypoventilation | Congenital pulmonary hypoventilation | Congenital central hypoventilation | Ondine's curse | CCHS - Congenital central hypoventilation (finding) | Primary alveolar hypoventilation
+BMGC_DS08208,BMG_DS031160,401138005,Pena-Shokeir syndrome type I,,,,,DOID:0111375,fetal akinesia deformation sequence syndrome,C1276035,,208150,MONDO:0100101,fetal akinesia deformation sequence 1,"Pena-Shokeir syndrome type I (disorder) | Pena-Shokeir syndrome type I | Fetal akinesia-hypokinesia sequence | Foetal akinesia-hypokinesia sequence | Arthrogryposis multiplex congenita, pulmonary hypoplasia syndrome | FADS - foetal akinesia deformation sequence | FADS - fetal akinesia deformation sequence"
+BMGC_DS08209,BMG_DS031175,402201001,Impetiginized atopic dermatitis,,,,,,,C1276076,,,,,Impetiginized atopic dermatitis (disorder) | Impetiginized atopic dermatitis | Infected atopic dermatitis
+BMGC_DS08210,BMG_DS031228,266005008,Infection due to Erysipelothrix rhusiopathiae (disorder),,,,,,,C1276801,,,MONDO:0006752,Erysipelothrix rhusiopathiae infectious disease,Infection caused by Erysipelothrix rhusiopathiae | Infection caused by Erysipelothrix insidiosa | Infection caused by Erysipelothrix rhusiopathiae (disorder)
+BMGC_DS08211,BMG_DS031257,178280004,Postnatal infection,,,,,,,C1278797,,,,,Postnatal infection | Postnatal infection (disorder)
+BMGC_DS08212,BMG_DS031259,236683007,Chlamydial urethritis,,,,,,,C1278807,,,,,Chlamydial urethritis | Inflammation of urethra caused by Chlamydia (disorder) | Inflammation of urethra caused by Chlamydia
+BMGC_DS08213,BMG_DS031262,267607008;182747006;54696002,Westphal disease,,,,,,,C1279186,C536694,,MONDO:0042980,Westphal disease,Familial periodic paralysis | Myoplegic dystrophy | Familial recurrent paralysis | Familial myoplegia | Cavarre disease | Periodic myotonia | Familial periodic paralysis (disorder) | Westphal disease | Westphal disease (disorder) | Familial periodic paralysis | Familial periodic paralysis (disorder)
+BMGC_DS08214,BMG_DS031290,198030008,periodic paralysis (finding),,,,,,,C1279412,,,MONDO:0016122,periodic paralysis,Periodic paralysis | Periodic paralysis (finding)
+BMGC_DS08215,BMG_DS031293,,X-Linked Combined Immunodeficiency Diseases,X-Linked Combined Immunodeficiency Diseases,,,,DOID:0060013,X-linked severe combined immunodeficiency,C1279481,D053632,300400,MONDO:0010315,T-B+ severe combined immunodeficiency due to gamma chain deficiency,
+BMGC_DS08216,BMG_DS031299,58950002;214600002,Tinea profunda (disorder),,,,,DOID:13368,tinea profunda,C1279621,,,MONDO:0001698,tinea profunda,Tinea profunda | Tinea profunda (disorder) | Tinea profunda | Majocchi's granuloma | Tinea profunda (disorder)
+BMGC_DS08217,BMG_DS031304,,,,,,,DOID:2800,acute interstitial pneumonia,C1279945,,,,,
+BMGC_DS08218,BMG_DS031310,248315005,Lipoatrophy,,,,,,,C1280433,,MTHU049594,,,Lipoatrophy | Lipoatrophy (disorder)
+BMGC_DS08219,BMG_DS031312,890181005,Podoconiosis,Elephantiasis,,,,DOID:0050138,podoconiosis,C1280469,D004604,,MONDO:0005425,podoconiosis,Podoconiosis (disorder) | Podoconiosis
+BMGC_DS08220,BMG_DS031319,,,,,,,,,C1280764,,244100,MONDO:0009481,Jumping Frenchmen of Maine,
+BMGC_DS08221,BMG_DS031322,,"Von Willebrand disease, platelet type",,,,,,,C1280798,C536458,177820,MONDO:0008332,platelet-type von Willebrand disease,
+BMGC_DS08222,BMG_DS031411,,Ocular Cicatricial Pemphigoid,"Pemphigoid, Benign Mucous Membrane",,,,,,C1282359,D010390,164185,MONDO:0008109,ocular cicatricial pemphigoid,
+BMGC_DS08223,BMG_DS031422,,,,,,,,,C1282500,,,MONDO:0041448,metastasis from malignant tumor of colon,
+BMGC_DS08224,BMG_DS031441,359643005,Enthesitis,,,,,,,C1282952,,,MONDO:0024419,enthesitis,Enthesitis | Enthesitis (disorder)
+BMGC_DS08225,BMG_DS031448,,"von Willebrand Disease, Type 2A","von Willebrand Disease, Type 2",,,,,,C1282968,D056728,,MONDO:0015628,von Willebrand disease type 2A,
+BMGC_DS08226,BMG_DS031449,,"von Willebrand Disease, Type 2B","von Willebrand Disease, Type 2",,,,,,C1282971,D056728,,MONDO:0015629,von Willebrand disease type 2B,
+BMGC_DS08227,BMG_DS031451,128111001;359729006,von Willebrand disease type 2M,,,,,,,C1282974,,,MONDO:0015630,von Willebrand disease type 2M,von Willebrand disease type 2M | von Willebrand disease type 2M (disorder)
+BMGC_DS08228,BMG_DS031452,,"von Willebrand Disease, Type 2N","von Willebrand Disease, Type 2",,,,,,C1282975,D056728,,MONDO:0015631,von Willebrand disease type 2N,
+BMGC_DS08229,BMG_DS031464,235658000;360375007,Lymphocytic gastritis,,,,,DOID:4035,lymphocytic gastritis,C1283271,,,MONDO:0002844,lymphocytic gastritis,Lymphocytic gastritis | Lymphocytic gastritis (disorder)
+BMGC_DS08230,BMG_DS031474,191397007,Butyrylcholinesterase deficiency,,,,,,,C1283400,C537417,617936,MONDO:0015270,butyrylcholinesterase deficiency,Serum cholinesterase defect | Butyrylcholinesterase deficiency | Plasma cholinesterase deficiency | Suxamethonium paralysis | Serum cholinesterase deficiency | Cholinesterase deficiency | Pseudocholinesterase deficiency | Pseudocholinesterase deficiency (disorder)
+BMGC_DS08231,BMG_DS031494,,"Sucrase-isomaltase deficiency, congenital",,,,,DOID:0111633,congenital sucrase-isomaltase deficiency,C1283620,C538139,222900,MONDO:0009114,congenital sucrase-isomaltase deficiency,
+BMGC_DS08232,BMG_DS031527,362975008,Degenerative disorder,,,,,DOID:1289,neurodegenerative disease,C1285162,,,,,Degenerative disorder | Degenerative disorder (disorder)
+BMGC_DS08233,BMG_DS031540,,Fetal Nutrition Disorders,Fetal Nutrition Disorders,,,,,,C1285261,D048070,,,,
+BMGC_DS08234,BMG_DS031543,363125002,Fetal ascites,,,,,,,C1285291,,MTHU003014,,,Fetal ascites (disorder) | Fetal ascites | Foetal ascites
+BMGC_DS08235,BMG_DS031599,55802003;367475009;359834003,Lesion of ulnar nerve,,8C10.1,Lesion of ulnar nerve,G56.2,DOID:12168,ulnar nerve lesion,C1288279,,,MONDO:0001458,ulnar nerve lesion,Ulnar neuropathy | Ulnar neuropathy (disorder) | Lesion of ulnar nerve | Lesion of ulnar nerve (disorder) | Ulnar nerve lesion | Ulnar nerve lesion (disorder)
+BMGC_DS08236,BMG_DS031601,12579009;84137001;367528006,Amyloid of familial Mediterranean fever,,,,,,,C1288287,,,,,Periodic disease | Paroxysmal polyserositis | Familial Mediterranean fever | Familial recurrent polyserositis | Familial paroxysmal polyserositis | Periodic polyserositis | Periodic peritonitis | Periodic familial peritonitis | MEF - Familial Mediterranean fever | Recurrent polyserositis | Benign paroxysmal peritonitis | FMF - Familial Mediterranean fever | Familial Mediterranean fever (disorder) | AA amyloidosis | AA amyloidosis (disorder) | Amyloid of familial Mediterranean fever | Amyloidosis due to familial Mediterranean fever (disorder) | Amyloidosis due to familial Mediterranean fever
+BMGC_DS08237,BMG_DS031662,48245008;111212009,Arthropathy associated with bacterial disease,,,,,,,C1290139,,,,,Bacterial arthritis | Arthritis due to bacterial infection | Bacterial arthritis (disorder) | Arthropathy associated with bacterial disease | Arthropathy associated with bacterial disease (disorder)
+BMGC_DS08238,BMG_DS031681,109298000,Subacute bursitis,,,,,,,C1290159,,,MONDO:0040698,subacute bursitis,Subacute bursitis | Subacute bursitis (disorder)
+BMGC_DS08239,BMG_DS031732,,,,,,,DOID:5090,sternum cancer,C1290244,,,MONDO:0021578,sternal neoplasm,
+BMGC_DS08240,BMG_DS031751,129452008,Nonspecific interstitial pneumonia,,,,,DOID:2801,nonspecific interstitial pneumonia,C1290344,,,MONDO:0019622,non-specific interstitial pneumonia,Nonspecific interstitial pneumonia | Nonspecific interstitial pneumonitis (disorder) | Nonspecific interstitial pneumonitis
+BMGC_DS08241,BMG_DS031753,,,,,,,DOID:7105,epiglottis neoplasm,C1290353,,,MONDO:0004109,epiglottis neoplasm,
+BMGC_DS08242,BMG_DS031754,,,,,,,DOID:5767,hilar lung neoplasm,C1290358,,,MONDO:0003639,lung hilum neoplasm,
+BMGC_DS08243,BMG_DS031755,128487001,Acute disease of cardiovascular system,,,,,,,C1290379,,,,,Acute disorder of cardiovascular system | Acute cardiovascular disorder | Acute cardiovascular disease | Acute disease of cardiovascular system | Acute disease of cardiovascular system (disorder)
+BMGC_DS08244,BMG_DS031760,128599005,Structural disorder of heart,,,,,,,C1290384,,,,,Structural disorder of heart | Structural disorder of heart (disorder)
+BMGC_DS08245,BMG_DS031775,,,,,,,DOID:5877,endocardium cancer,C1290401,,,MONDO:0021378,neoplasm of endocardium,
+BMGC_DS08246,BMG_DS031776,,,,,,,DOID:9299,myocardium cancer,C1290402,,,MONDO:0021380,neoplasm of myocardium,
+BMGC_DS08247,BMG_DS031777,,,,,,,DOID:4699,epicardium cancer,C1290403,,,MONDO:0021379,neoplasm of epicardium,
+BMGC_DS08248,BMG_DS031778,,,,,,,DOID:175,vascular cancer,C1290407,,,,,
+BMGC_DS08249,BMG_DS032021,,3-Hydroxyacyl-CoA Dehydrogenase Deficiency,,,,,,,C1291230,C535310,231530,MONDO:0017715,3-hydroxyacyl-CoA dehydrogenase deficiency,
+BMGC_DS08250,BMG_DS032036,,Cortisone reductase deficiency,,,,,DOID:0090139,cortisone reductase deficiency,C1291245,C536447,,MONDO:0000193,cortisone reductase deficiency,
+BMGC_DS08251,BMG_DS032090,124204003,Deficiency of iodide peroxidase (disorder),,,,,,,C1291299,,274500,MONDO:0010133,thyroid dyshormonogenesis 2A,Deficiency of iodinase | Deficiency of iodide peroxidase | Deficiency of iodide peroxidase (disorder)
+BMGC_DS08252,BMG_DS032120,,Transaldolase Deficiency,,,,,,,C1291329,C563207,606003,MONDO:0011624,transaldolase deficiency,
+BMGC_DS08253,BMG_DS032162,124309005,Deficiency of sedoheptulokinase,,,,,,,C1291373,,617213,MONDO:0014969,isolated sedoheptulokinase deficiency,Deficiency of heptulokinase | Deficiency of sedoheptulokinase | Deficiency of sedoheptulokinase (disorder)
+BMGC_DS08254,BMG_DS032175,,D-glycericacidemia,,,,E72.59,DOID:0111626,D-glyceric aciduria,C1291386,C535767,,,,
+BMGC_DS08255,BMG_DS032190,124343001,Phosphoribosylpyrophosphate synthetase deficiency,,,,,,,C1291401,C537897,,MONDO:0043176,phosphoribosylpyrophosphate synthetase deficiency,Deficiency of ribose-phosphate pyrophosphokinase | Deficiency of ribose-phosphate pyrophosphokinase (disorder) | Phosphoribosylpyrophosphate synthetase deficiency
+BMGC_DS08256,BMG_DS032249,124432005,Deficiency of phosphoserine phosphatase,,,,,,,C1291463,,614023,MONDO:0013531,PSPH deficiency,Deficiency of choline phosphatase | Deficiency of phosphoserine phosphatase | Deficiency of phosphoserine phosphatase (disorder)
+BMGC_DS08257,BMG_DS032275,,Hyaluronidase Deficiency,,,,,,,C1291490,C563209,601492,MONDO:0011093,mucopolysaccharidosis type 9,
+BMGC_DS08258,BMG_DS032297,,Beta-Ureidopropionase Deficiency,,,,,,,C1291512,C563210,613161,MONDO:0013164,beta-ureidopropionase deficiency,
+BMGC_DS08259,BMG_DS032344,124597000,Deficiency of phosphoribosylaminoimidazole carboxylase,,,,,,,C1291561,,619859,MONDO:0859244,phosphoribosylaminoimidazole carboxylase deficiency,Deficiency of phosphoribosylaminoimidazole carboxylase | Deficiency of phosphoribosylaminoimidazole carboxylase (disorder)
+BMGC_DS08260,BMG_DS032347,124600004,Deficiency of aromatic-L-amino-acid decarboxylase,,,,,DOID:0090123,aromatic L-amino acid decarboxylase deficiency,C1291564,,608643,MONDO:0012084,aromatic L-amino acid decarboxylase deficiency,Deficiency of tryptophan decarboxylase | Deficiency of hydroxytryptophan decarboxylase | Deficiency of dopa decarboxylase | Deficiency of aromatic-L-amino-acid decarboxylase | Deficiency of aromatic-L-amino-acid decarboxylase (disorder)
+BMGC_DS08261,BMG_DS032389,124664006,Deficiency of maleylacetoacetate isomerase,,,,,,,C1291607,,617596,MONDO:0060527,maleylacetoacetate isomerase deficiency,Deficiency of maleylacetoacetate isomerase | Deficiency of maleylacetoacetate isomerase (disorder) | GSTZ1-gene related deficiency of maleylacetoacetate isomerase
+BMGC_DS08262,BMG_DS032391,,Ribose 5-Phosphate Isomerase Deficiency,,,,,,,C1291609,C563212,608611,MONDO:0012073,ribose-5-P isomerase deficiency,
+BMGC_DS08263,BMG_DS032402,124678007,Deficiency of bisphosphoglycerate mutase,,,,,,,C1291620,,222800,MONDO:0009113,hemolytic anemia due to diphosphoglycerate mutase deficiency,Deficiency of glycerate phosphomutase | Deficiency of diphosphoglycerate mutase | Deficiency of bisphosphoglycerate synthase | Deficiency of bisphosphoglycerate mutase | Deficiency of bisphosphoglycerate mutase (disorder)
+BMGC_DS08264,BMG_DS032437,,,,,,,,,C1292754,,,MONDO:0020323,primary mediastinal large B-cell lymphoma,
+BMGC_DS08265,BMG_DS032438,,,,,,,,,C1292758,,,MONDO:0044917,T-lymphoblastic lymphoma,
+BMGC_DS08266,BMG_DS032440,,,,,,,DOID:0060597,"atypical chronic myeloid leukemia, BCR-ABL1 negative",C1292772,,,MONDO:0004653,"atypical chronic myeloid leukemia, BCR-ABL1 negative",
+BMGC_DS08267,BMG_DS032441,,,,,,,,,C1292773,,,MONDO:0019456,acute myeloid leukemia with multilineage dysplasia,
+BMGC_DS08268,BMG_DS032442,,,,,,,,,C1292774,,,MONDO:0015166,acute myeloid leukemia with t(8;21)(q22;q22) translocation,
+BMGC_DS08269,BMG_DS032443,,,,,,,,,C1292775,,,MONDO:0020317,acute myeloid leukemia with 11q23 abnormalities,
+BMGC_DS08270,BMG_DS032444,,,,,,,,,C1292776,,,MONDO:0019457,therapy related acute myeloid leukemia and myelodysplastic syndrome,
+BMGC_DS08271,BMG_DS032445,,,,,,,DOID:1035,aggressive NK-cell leukemia,C1292777,,,MONDO:0019470,aggressive NK-cell leukemia,
+BMGC_DS08272,BMG_DS032446,,,,,,,DOID:2226,myeloproliferative neoplasm,C1292778,,,MONDO:0020076,myeloproliferative neoplasm,
+BMGC_DS08273,BMG_DS032453,373607009,Oxalosis,Hyperoxaluria,,,E72.53,,,C1298681,D006959,,,,Oxalosis (disorder) | Oxalosis
+BMGC_DS08274,BMG_DS032456,,,,,,,,,C1298692,,,MONDO:0015420,cleft lip and alveolus,
+BMGC_DS08275,BMG_DS032604,,,,,,,DOID:7519,endocervical carcinoma,C1299237,,,MONDO:0004259,endocervical carcinoma,
+BMGC_DS08276,BMG_DS032605,,,,,,,DOID:2892,exocervical carcinoma,C1299238,,,MONDO:0002455,exocervical carcinoma,
+BMGC_DS08277,BMG_DS032606,,,,,,,DOID:7764,subglottis carcinoma,C1299239,,,MONDO:0004358,subglottis carcinoma,
+BMGC_DS08278,BMG_DS032607,,,,,,,DOID:7763,carcinoma of supraglottis,C1299240,,,MONDO:0004357,carcinoma of supraglottis,
+BMGC_DS08279,BMG_DS032608,,,,,,,DOID:2394,ovarian cancer,C1299247,,,,,
+BMGC_DS08280,BMG_DS032610,,Left Main Coronary Artery Disease,Coronary Artery Disease,,,,,,C1299433,D003324,,,,
+BMGC_DS08281,BMG_DS032638,371139006,Early cirrhosis,,,,,,,C1299579,,,,,Early cirrhosis (disorder) | Early cirrhosis
+BMGC_DS08282,BMG_DS032650,,Postural Orthostatic Tachycardia Syndrome,Postural Orthostatic Tachycardia Syndrome,,,,DOID:0111154,postural orthostatic tachycardia syndrome,C1299624,D054972,604715,MONDO:0011479,postural orthostatic tachycardia syndrome,
+BMGC_DS08283,BMG_DS032661,371100002,Extravasation injury,,,,,,,C1299641,,,,,Extravasation injury (disorder) | Extravasation injury
+BMGC_DS08284,BMG_DS032676,370474006,Eosinophilic myositis (disorder),,,,,,,C1299884,,,,,Eosinophilic myositis (disorder) | Eosinophilic myositis
+BMGC_DS08285,BMG_DS032717,,,,,,,DOID:2643,perivascular epithelioid cell tumor,C1300127,,,MONDO:0006359,neoplasm with perivascular epithelioid cell differentiation,
+BMGC_DS08286,BMG_DS032718,4839005,Chronic enlargement of lacrimal gland,,,,H04.03,DOID:12809,chronic lacrimal gland enlargement,C1300133,,,MONDO:0001588,chronic lacrimal gland enlargement,Chronic enlargement of lacrimal gland | Chronic lacrimal gland enlargement | Chronic enlargement of lacrimal gland (disorder)
+BMGC_DS08287,BMG_DS032724,389264005,Genochondromatosis,,,,,,,C1300229,C563215,137360,MONDO:0007653,genochondromatosis,Genochondromatosis (disorder) | Genochondromatosis
+BMGC_DS08288,BMG_DS032731,389158007,"Thanatophoric dysplasia, type 2",,,,,,,C1300257,C536508,187601,MONDO:0008547,thanatophoric dysplasia type 2,"Thanatophoric dysplasia, type 2 (disorder) | Thanatophoric dysplasia, type 2"
+BMGC_DS08289,BMG_DS032732,,"Spondyloepimetaphyseal dysplasia, sponastrime type",,,,,,,C1300260,C535786,271510,MONDO:0010068,"spondyloepimetaphyseal dysplasia, sponastrime type",
+BMGC_DS08290,BMG_DS032738,389169005,Brachydactyly syndrome type C,,,,,DOID:0110970,brachydactyly type C,C1300268,,,,,Brachydactyly syndrome type C (disorder) | Brachydactyly syndrome type C
+BMGC_DS08291,BMG_DS032743,,SAUL-WILSON SYNDROME,,,,,DOID:0111673,Saul-Wilson syndrome,C1300285,,606976;618150,MONDO:0019407,"microcephalic osteodysplastic dysplasia, Saul-Wilson type",
+BMGC_DS08292,BMG_DS032744,389201004,Transient neonatal hyperparathyroidism,,,,,,,C1300287,,618188,MONDO:0032591,"hyperparathyroidism, transient neonatal",Transient neonatal hyperparathyroidism (disorder) | Transient neonatal hyperparathyroidism
+BMGC_DS08293,BMG_DS032749,,,,,,,DOID:4993,atypical polypoid adenomyoma,C1300347,,,MONDO:0003236,atypical polypoid adenomyoma,
+BMGC_DS08294,BMG_DS032752,,,,,,,DOID:7141,prostate small cell carcinoma,C1300585,,,MONDO:0006390,prostate small cell carcinoma,
+BMGC_DS08295,BMG_DS032757,,,,,,,DOID:7716,mixed ductal-endocrine carcinoma,C1301048,,,MONDO:0004340,mixed ductal-endocrine carcinoma of pancreas,
+BMGC_DS08296,BMG_DS032764,,,,,,,DOID:4324,acantholytic acanthoma,C1301270,,,MONDO:0002963,acantholytic acanthoma,
+BMGC_DS08297,BMG_DS032766,,,,,,,DOID:4972,myelodysplastic/myeloproliferative neoplasm,C1301355,,,MONDO:0006311,myelodysplastic/myeloproliferative neoplasm,
+BMGC_DS08298,BMG_DS032767,,,,,,,,,C1301357,,,MONDO:0019460,acute leukemia of ambiguous lineage,
+BMGC_DS08299,BMG_DS032769,,,,,,,,,C1301362,,,MONDO:0017598,primary cutaneous anaplastic large cell lymphoma,
+BMGC_DS08300,BMG_DS032770,,,,,,,,,C1301363,,,MONDO:0019467,CD4+/CD56+ hematodermic neoplasm,
+BMGC_DS08301,BMG_DS032771,,,,,,,DOID:7849,dendritic cell sarcoma,C1301364,,,MONDO:0004380,dendritic cell sarcoma,
+BMGC_DS08302,BMG_DS032772,,,,,,,DOID:4797,SM-AHNMD,C1301365,,,MONDO:0020332,systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease,
+BMGC_DS08303,BMG_DS032782,397541004,Severe visual impairment,,,,,,,C1301509,,MTHU006121,,,Severe visual impairment (disorder) | Severe visual impairment
+BMGC_DS08304,BMG_DS032784,397552005,Vaccinia keratitis,,,,,,,C1301518,,,,,Vaccinia keratitis (disorder) | Vaccinia keratitis
+BMGC_DS08305,BMG_DS032795,6758009;46764007;397748008,Hypertension with albuminuria,,,,,,,C1301626,,,,,"Pre-eclamptic toxemia | Pre-eclampsia | Pre-eclampsia (disorder) | PET - Pre-eclamptic toxaemia | EPH - Oedema, proteinuria and hypertension of pregnancy | Pre-eclamptic toxaemia | PET - Pre-eclamptic toxemia | EPH - Edema, proteinuria and hypertension of pregnancy | Hypertension with albuminuria | Gestosis | PE - Pre-eclampsia | Proteinuric hypertension of pregnancy | Severe pre-eclampsia | Severe pre-eclamptic toxemia | Severe pre-eclamptic toxaemia | Severe pre-eclampsia (disorder) | PET - Severe pre-eclamptic toxaemia | PET - Severe pre-eclamptic toxemia | Severe proteinuric hypertension of pregnancy | Hypertension with albuminuria (disorder) | Hypertension with albuminuria"
+BMGC_DS08306,BMG_DS032821,,,,,,,,,C1302401,,,MONDO:0005484,colorectal adenoma,
+BMGC_DS08307,BMG_DS032825,,,,,,,DOID:10287,prostate squamous cell carcinoma,C1302530,,,MONDO:0000993,prostate squamous cell carcinoma,
+BMGC_DS08308,BMG_DS032827,,,,,,,DOID:6354,chronic lymphocytic leukemia/small lymphocytic lymphoma,C1302547,,,MONDO:0003864,chronic lymphocytic leukemia/small lymphocytic lymphoma,
+BMGC_DS08309,BMG_DS032828,,,,,,,DOID:5207,monodermal teratoma,C1302569,,,MONDO:0003331,ovarian monodermal teratoma,
+BMGC_DS08310,BMG_DS032844,,,,,,,,,C1302740,,228020,MONDO:0009219,"fascial dystrophy, congenital",
+BMGC_DS08311,BMG_DS032873,,,,,,,,,C1302848,,,MONDO:0044656,epidermolytic nevus,
+BMGC_DS08312,BMG_DS032887,,,,,,,,,C1302995,,,MONDO:0007614,congenital fibrosis of extraocular muscles,
+BMGC_DS08313,BMG_DS032896,,,,,,,,,C1303009,,156600,MONDO:0007989,congenital microcoria,
+BMGC_DS08314,BMG_DS032899,,Nicolaides Baraitser syndrome,,,,,,,C1303073,C536116,601358,MONDO:0011053,intellectual disability-sparse hair-brachydactyly syndrome,
+BMGC_DS08315,BMG_DS032905,401303003,Acute ST segment elevation myocardial infarction (disorder),,,,,,,C1303258,,,,,Acute ST segment elevation myocardial infarction (disorder) | Acute ST segment elevation myocardial infarction | STEMI - ST elevation myocardial infarction
+BMGC_DS08316,BMG_DS033048,402382008,Idiopathic angioedema,,,,,,,C1304177,,,,,Idiopathic angioedema (disorder) | Idiopathic angio-oedema | Idiopathic angioedema
+BMGC_DS08317,BMG_DS033060,,Autoimmune Urticaria,Chronic Urticaria,,,,DOID:0080747,chronic urticaria,C1304191,D000080223,,MONDO:0025513,autoimmune urticaria,
+BMGC_DS08318,BMG_DS033062,,Chronic Autoimmune Urticaria,Chronic Urticaria,,,,DOID:0080747,chronic urticaria,C1304193,D000080223,,,,
+BMGC_DS08319,BMG_DS033105,402463003,Familial localized cutaneous amyloidosis,,,,,,,C1304242,,,MONDO:0007101,familial primary localized cutaneous amyloidosis,Familial localized cutaneous amyloidosis (disorder) | Familial localised cutaneous amyloidosis | Familial localized cutaneous amyloidosis
+BMGC_DS08320,BMG_DS033124,,,,,,,DOID:4290,adamantinoid basal cell epithelioma,C1304295,,,MONDO:0002947,adamantinoid basal cell epithelioma,
+BMGC_DS08321,BMG_DS033127,,,,,,,DOID:4280,nodular basal cell carcinoma,C1304300,,,,,
+BMGC_DS08322,BMG_DS033271,403803002,Linear and whorled nevoid hypermelanosis,,,,,,,C1304501,,614323,MONDO:0013688,linear and whorled nevoid hypermelanosis,Linear and whorled nevoid hypermelanosis (disorder) | Linear and whorled naevoid hypermelanosis | Linear and whorled nevoid hypermelanosis
+BMGC_DS08323,BMG_DS033276,,,,,,,DOID:496,spindle cell hemangioma,C1304508,,,MONDO:0016222,spindle cell hemangioma,
+BMGC_DS08324,BMG_DS033277,,,,,,,DOID:5236,subungual glomus tumor,C1304510,,,MONDO:0003341,subungual glomus tumor,
+BMGC_DS08325,BMG_DS033278,,,,,,,DOID:486,glomeruloid hemangioma,C1304511,,,MONDO:0003172,glomeruloid hemangioma,
+BMGC_DS08326,BMG_DS033281,1295240006;403990005,Ischemic fasciitis,,,,,DOID:9601,ischemic fasciitis,C1304514,,,MONDO:0004834,ischemic fasciitis,Ischaemic fasciitis | Ischemic fasciitis (morphologic abnormality) | Ischemic fasciitis | Ischemic fasciitis (disorder) | Ischaemic fasciitis | Ischemic fasciitis
+BMGC_DS08327,BMG_DS033289,195265003,"Thoracoabdominal aortic aneurysm, ruptured",,BD50.51,Thoracoabdominal aortic aneurysm with rupture,I71.5,DOID:3627,aortic aneurysm,C1305122,,,,,"Thoracoabdominal aortic aneurysm, ruptured | Thoracoabdominal aortic aneurysm, ruptured (disorder)"
+BMGC_DS08328,BMG_DS033292,,,,,,,DOID:3615,infiltrating angiolipoma,C1305256,,,MONDO:0002710,infiltrating angiolipoma,
+BMGC_DS08329,BMG_DS033296,23260002;270893004,Fibroadenosis of breast,,GB20.1,Fibroadenosis of breast,N60.2,DOID:10352,breast fibroadenosis,C1305875,,,,,Fibroadenosis of breast | Fibroadenosis of breast (disorder) | Fibroadenosis breast | Breast: [fibroadenosis] or [adenosis] | Adenosis - breast | Fibroadenosis of breast | Fibroadenosis - breast | Breast: [fibroadenosis] or [adenosis] (disorder)
+BMGC_DS08330,BMG_DS033298,57333009;399094007,Familial hematuria,,,,,,,C1305904,,,,,Hereditary nephritis | Alport's syndrome | Familial nephritis | Familial hematuria | Hereditary glomerulonephritis | GN - Hereditary glomerulonephritis | Non-progressive hereditary glomerulonephritis | Benign familial haematuria | Benign familial hematuria | Familial haematuria | Hereditary nephritis (disorder) | Familial hematuria (disorder) | Familial haematuria | Familial hematuria
+BMGC_DS08331,BMG_DS033302,,,,,,,,,C1305934,,,MONDO:0004808,benign mammary dysplasia,
+BMGC_DS08332,BMG_DS033321,,,,,,,,,C1306065,,142700,MONDO:0007729,developmental dysplasia of the hip 1,
+BMGC_DS08333,BMG_DS033324,193687000,Oguchi disease,,,,,DOID:8498;DOID:0050534,hereditary night blindness | congenital stationary night blindness,C1306122,C537743,,MONDO:0019152,Oguchi disease,Oguchi's disease | Oguchi's disease (disorder) | Oguchi disease
+BMGC_DS08334,BMG_DS033328,,,,,,,DOID:7004,ACTH-secreting pituitary adenoma,C1306214,,,MONDO:0006068,ACTH-producing pituitary gland adenoma,
+BMGC_DS08335,BMG_DS033333,,,,,,,DOID:3205,melanotic neurilemmoma,C1306247,,,MONDO:0002558,melanotic neurilemmoma,
+BMGC_DS08336,BMG_DS033338,,,,,,,DOID:0060327;DOID:0060321,omphalocele | umbilical hernia,C1306503,,,,,
+BMGC_DS08337,BMG_DS033339,20696009,Chronic venous insufficiency,,,,,,,C1306557,,,MONDO:0000492,chronic venous insufficiency,Peripheral venous insufficiency | Chronic venous insufficiency | Peripheral venous insufficiency (disorder)
+BMGC_DS08338,BMG_DS033341,,,,,,,DOID:3255,botryoid rhabdomyosarcoma,C1306573,,,,,
+BMGC_DS08339,BMG_DS033344,35610006;2776000,Acute encephalopathy,,,,,,,C1306587,,MTHU004221,,,Acute brain syndrome | Acute brain syndrome (disorder) | Delirium | Organic brain syndrome | Acute confusional state | OBS - Organic brain syndrome | Acute psycho-organic syndrome | Acute organic reaction | ABS - Acute brain syndrome | Acute brain syndrome | Delirium (disorder)
+BMGC_DS08340,BMG_DS033345,68870007,"Congenital dyserythropoietic anemia, type II",,,,,DOID:0111401,congenital dyserythropoietic anemia type II,C1306589,,224100,MONDO:0009134,congenital dyserythropoietic anemia type 2,"Congenital dyserythropoietic anemia, type II | Congenital dyserythropoietic anaemia, type II | Congenital dyserythropoietic anemia, type II (disorder) | Hereditary erythroblast multinuclearity with positive acid serum test | HEMPAS - hereditary erythroblast multinuclearity with positive acid serum test"
+BMGC_DS08341,BMG_DS033357,,Wound Botulism,Botulism,,,,,,C1306794,D001906,,MONDO:0015803,wound botulism,
+BMGC_DS08342,BMG_DS033362,18018005;361126006,Subacute lymphocytic thyroiditis,,,,,DOID:7187,subacute lymphocytic thyroiditis,C1306804,,,MONDO:0004135,subacute lymphocytic thyroiditis,Self-limiting autoimmune thyroiditis with transient hyperthyroidism and/or hypothyroidism | Self-limiting autoimmune thyroiditis with transient hyperthyroidism and/or hypothyroidism (disorder) | Subacute lymphocytic thyroiditis | Subacute lymphocytic thyroiditis (disorder)
+BMGC_DS08343,BMG_DS033364,399114005;8753005;36527001,Periarthritis of shoulder,,FB53.0,Adhesive capsulitis of shoulder,M75.0,,,C1306835,,,,,Adhesive capsulitis of shoulder (disorder) | Adhesive capsulitis of shoulder | Duplay's periarthritis syndrome | Pericapsulitis of shoulder | Frozen shoulder | Periarthritis of shoulder | Duplay periarthritis syndrome | Adhesive capsulitis of shoulder | Scapulohumeral fibrositis | Frozen shoulder | Scapulohumeral myofibrosis | Duplay's periarthritis syndrome | Periarthritis of shoulder | Pericapsulitis of shoulder | Adhesive capsulitis of shoulder (disorder) | Periarthritis of shoulder | Periarthritis of shoulder (disorder)
+BMGC_DS08344,BMG_DS033365,,,,,,,DOID:4465,papillary renal cell carcinoma,C1306837,,,MONDO:0017884,papillary renal cell carcinoma,
+BMGC_DS08345,BMG_DS033366,224729007;267888004;80843008;69896004,Proliferative arthritis,,,,,,,C1306838,,,,,Proliferative arthritis | Hypertrophic polyarthritis | Hypertrophic arthritis | Proliferative arthritis (disorder) | Osteoarthritis | Degenerative arthritis | OA - Osteoarthritis | Osteoarthrosis | OA - Osteoarthrosis | Osteoarthritis (disorder) | Degenerative arthropathy | Hypertrophic polyarthritis | Proliferative arthritis | Hypertrophic arthritis | Degenerative polyarthritis | Degenerative joint disease | Degenerative joint disease | Osteoarthrosis | Degenerative arthritis | Degenerative polyarthritis | Hypertrophic arthritis | Hypertrophic polyarthritis | Osteoarthritis | Proliferative arthritis | Degenerative arthropathy | Degenerative joint disease (disorder) | Rheumatoid arthritis | Atrophic arthritis | Rheumatic gout | Rheumatoid arthritis (disorder) | RA - Rheumatoid arthritis | Rheumatoid disease | RhA - Rheumatoid arthritis | Proliferative arthritis
+BMGC_DS08346,BMG_DS033375,399957001;91523003,Peripheral arterial occlusive disease,,,,,,,C1306889,,,,,Peripheral arterial occlusive disease (disorder) | Peripheral arterial occlusive disease | PAOD - Peripheral arterial occlusive disease | Peripheral angiopathy | Peripheral artery occlusive disease | Peripheral vascular disease | Peripheral angiopathy | Peripheral vascular disease (disorder) | Peripheral arterial occlusive disease | PVD - Peripheral vascular disease | Peripheral arterial disease | PAOD - Peripheral arterial occlusive disease
+BMGC_DS08347,BMG_DS033377,75127007;205542007,Hereditary edema of legs,,,,,DOID:0050580,hereditary lymphedema,C1313885,,,,,Hereditary edema of legs | Congenital lymphedema | Hereditary trophedema | Milroy's disease | Hereditary trophoedeme | Hereditary trophoedema | Hereditary oedema of legs | Congenital lymphoedema | Hereditary edema of legs (disorder) | Primary (congenital) lymphoedema | Primary (congenital) lymphedema | Hereditary edema of legs | Hereditary oedema of legs | Hereditary edema of legs (disorder)
+BMGC_DS08348,BMG_DS033380,,Trichorrhexis nodosa syndrome,,,,,,,C1313961,C536556,234050,MONDO:0021013,"trichothiodystrophy 4, nonphotosensitive",
+BMGC_DS08349,BMG_DS033383,240066005;17482009,Acute contagious conjunctivitis,,,,,DOID:11213,acute contagious conjunctivitis,C1313983,,,MONDO:0001226,acute contagious conjunctivitis,Acute contagious conjunctivitis | Acute contagious conjunctivitis (disorder) | Mucopurulent conjunctivitis | Mucopurulent conjunctivitis (disorder)
+BMGC_DS08350,BMG_DS033386,48194001,Hypertension complicating childbirth,,,,,,,C1314752,,,,,Pregnancy-induced hypertension | GH - Gestational hypertension | Gestational hypertension | Hypertension induced by pregnancy | PIH - Pregnancy-induced hypertension | Pregnancy-induced hypertension (disorder)
+BMGC_DS08351,BMG_DS033388,200973000;65539006,Impetigo herpetiformis,,EA90.40,Generalised pustular psoriasis,L40.1,DOID:0080474;DOID:8503,impetigo herpetiformis | pustular psoriasis 14,C1314968,,,MONDO:0004591,impetigo herpetiformis,Pustular psoriasis | Pustular psoriasis (disorder) | Impetigo herpetiformis | Impetigo herpetiformis (disorder)
+BMGC_DS08352,BMG_DS033398,11791001,Necrotizing vasculitis,,,,,,,C1318520,,,MONDO:0800113,necrotizing vasculitis,Necrotizing vasculitis | Necrotising vasculitis | Necrotizing vasculitis (disorder)
+BMGC_DS08353,BMG_DS033400,,,,,,,DOID:2834,acquired polycythemia,C1318533,,,MONDO:0020115,secondary polycythemia,
+BMGC_DS08354,BMG_DS033401,,,,,,,DOID:314,tenosynovial giant cell tumor,C1318543,,,MONDO:0002522,tenosynovial giant cell tumor,
+BMGC_DS08355,BMG_DS033403,,,,,,,,,C1318550,,,MONDO:0015040,myelodysplastic syndrome with excess blasts-1,
+BMGC_DS08356,BMG_DS033405,,,,,,,DOID:0111359,large congenital melanocytic nevus,C1318558,,,,,
+BMGC_DS08357,BMG_DS033406,171847006;399095008,Fusospirochetal pharyngitis,,1C4Z,Unspecified bacterial disease,A69.1,,,C1318559,,,,,Fusospirochetosis | ANUG | Acute ulcerative gingivitis | Vincent's angina | Acute ulceromembranous gingivitis | Trench mouth | Vincent's gingivitis | Acute necrotizing ulcerative stomatitis | Acute necrotising ulcerative gingivitis | Fusospirochetal pharyngitis | Spirochetal stomatitis | Acute necrotizing ulcerative gingivitis | Spirochaetal stomatitis | Fusospirochaetal pharyngitis | Acute necrotising ulcerative stomatitis | Acute necrotizing ulcerative gingivitis (disorder) | Fusospirochetal pharyngitis (disorder) | Fusospirochaetal pharyngitis | Fusospirochetal pharyngitis
+BMGC_DS08358,BMG_DS033417,406602003,Staphylococcus aureus infection,,,,,,,C1318973,,,MONDO:0005545,staphylococcus aureus infection,Staphylococcus aureus infection | Infection caused by Staphylococcus aureus (disorder) | Infection caused by Staphylococcus aureus
+BMGC_DS08359,BMG_DS033442,,,,,,,DOID:0050861,colorectal adenocarcinoma,C1319315,,,MONDO:0005008,colorectal adenocarcinoma,
+BMGC_DS08360,BMG_DS033443,,,,,,,,,C1319317,,,MONDO:0000536,pharyngeal squamous cell carcinoma,
+BMGC_DS08361,BMG_DS033448,,Barber Say syndrome,,,,,DOID:0060549,Barber-Say syndrome,C1319466,C537908,209885,MONDO:0008853,Barber-Say syndrome,
+BMGC_DS08362,BMG_DS033453,,"Asthma, Aspirin-Induced","Asthma, Aspirin-Induced",,,,,,C1319853,D055963,,,,
+BMGC_DS08363,BMG_DS033476,406574007,Infection caused by Enterococcus,,,,,,,C1320183,,,,,Infection caused by Enterococcus | Infection caused by Enterococcus (disorder)
+BMGC_DS08364,BMG_DS033518,,,,,,,DOID:8082,cellular congenital mesoblastic nephroma,C1320471,,,MONDO:0004454,cellular congenital mesoblastic nephroma,
+BMGC_DS08365,BMG_DS033520,405821001,Allergic otitis externa,,,,,,,C1320547,,,,,Allergic otitis externa (disorder) | Allergic otitis externa
+BMGC_DS08366,BMG_DS033523,61536007;193393004;95704002,Peripheral retinal degeneration,,9B78.4,Peripheral retinal degeneration,H35.4,DOID:12161,peripheral retinal degeneration,C1320640,,,MONDO:0001451,peripheral retinal degeneration,Peripheral retinal degeneration | Peripheral retinal degeneration (disorder) | Peripheral degeneration of retina | Peripheral retinal degeneration | Peripheral retinal degeneration (disorder) | Retinal atrophy | Retina atrophic | Peripheral retinal degeneration | Retina atrophic (disorder)
+BMGC_DS08367,BMG_DS033538,,Drug-induced Hepatic Necrosis,Massive Hepatic Necrosis,,,,,,C1320834,D047508,,,,
+BMGC_DS08368,BMG_DS033551,405566004,Paraneoplastic hyponatremia,,,,,,,C1321135,,,,,Paraneoplastic hyponatremia (disorder) | Paraneoplastic hyponatraemia | Paraneoplastic hyponatremia
+BMGC_DS08369,BMG_DS033555,,,,,,,DOID:2996,mixed germ cell-sex cord neoplasm,C1321220,,,MONDO:0002478,mixed germ cell-sex cord-stromal tumor,
+BMGC_DS08370,BMG_DS033578,,,,,,,DOID:8353,epithelioid malignant peripheral nerve sheath tumor,C1321427,,,MONDO:0004540,epithelioid malignant peripheral nerve sheath tumor,
+BMGC_DS08371,BMG_DS033589,403443000,Behçet's disease affecting oral mucosa,,,,,,,C1321482,,,,,Behçet's disease affecting oral mucosa (disorder) | Behçet's disease affecting oral mucosa | Oral ulceration due to Behçet's disease | Behçet disease affecting oral mucosa
+BMGC_DS08372,BMG_DS033591,,,,,,,DOID:0050465,Muir-Torre syndrome,C1321489,,158320,MONDO:0008018,Muir-Torre syndrome,
+BMGC_DS08373,BMG_DS033595,,,,,,,,,C1321495,,102100,MONDO:0007050,"acromegaloid changes, cutis verticis gyrata, and corneal leukoma",
+BMGC_DS08374,BMG_DS033599,719069008;83092002,Shprintzen-Goldberg syndrome,,,,,,,C1321551,,182212,MONDO:0008426,Shprintzen-Goldberg syndrome,Shprintzen Goldberg craniosynostosis syndrome (disorder) | Shprintzen Goldberg craniosynostosis syndrome | Marfanoid craniosynostosis syndrome | Shprintzen-Goldberg syndrome | Shprintzen syndrome | Velo-cardio-facial syndrome | Shprintzen syndrome (disorder) | Velocardiofacial syndrome | VCF-Velocardiofacial syndrome | 22q11 microdeletion with velocardiofacial syndrome phenotype
+BMGC_DS08375,BMG_DS033604,,,,,,,DOID:11684,melanoacanthoma,C1321683,,,MONDO:0006579,melanoacanthoma,
+BMGC_DS08376,BMG_DS033605,,,,,,,DOID:6344,melanotic psammomatous malignant peripheral nerve sheath tumor,C1321709,,,MONDO:0003862,melanotic psammomatous malignant peripheral nerve sheath tumor,
+BMGC_DS08377,BMG_DS033609,6758009;173300003;46764007,Gestosis,,,,,,,C1321782,,,,,"Pre-eclamptic toxemia | Pre-eclampsia | Pre-eclampsia (disorder) | PET - Pre-eclamptic toxaemia | EPH - Oedema, proteinuria and hypertension of pregnancy | Pre-eclamptic toxaemia | PET - Pre-eclamptic toxemia | EPH - Edema, proteinuria and hypertension of pregnancy | Hypertension with albuminuria | Gestosis | PE - Pre-eclampsia | Proteinuric hypertension of pregnancy | Disorder of pregnancy | Disorder of pregnancy (disorder) | Severe pre-eclampsia | Severe pre-eclamptic toxemia | Severe pre-eclamptic toxaemia | Severe pre-eclampsia (disorder) | PET - Severe pre-eclamptic toxaemia | PET - Severe pre-eclamptic toxemia | Severe proteinuric hypertension of pregnancy"
+BMGC_DS08378,BMG_DS033611,,,,,,,DOID:3079,childhood astrocytic tumor,C1321865,,,MONDO:0002505,childhood astrocytic tumor,
+BMGC_DS08379,BMG_DS033612,,,,,,,DOID:6938,childhood intraocular retinoblastoma,C1321869,,,MONDO:0004045,pediatric intraocular retinoblastoma,
+BMGC_DS08380,BMG_DS033613,,,,,,,DOID:7747,childhood extraocular retinoblastoma,C1321870,,,MONDO:0004350,pediatric extraocular retinoblastoma,
+BMGC_DS08381,BMG_DS033616,,,,,,,DOID:2095,sweat gland cancer,C1321904,,,MONDO:0002206,sweat gland cancer,
+BMGC_DS08382,BMG_DS033619,,,,,,,DOID:3774,chordoid glioma,C1322252,,,MONDO:0016706,chordoid glioma of the third ventricle,
+BMGC_DS08383,BMG_DS033622,,,,,,,DOID:4554,type C thymoma,C1322286,,,,,
+BMGC_DS08384,BMG_DS033624,,,,,,,DOID:2781,rectosigmoid cancer,C1327709,,,MONDO:0002424,rectosigmoid carcinoma,
+BMGC_DS08385,BMG_DS033625,,,,,,,DOID:0090118,congenital amegakaryocytic thrombocytopenia,C1327915,,,MONDO:0800451,congenital amegakaryocytic thrombocytopenia,
+BMGC_DS08386,BMG_DS033626,,,,,,,,,C1327916,,268130,MONDO:0009990,Revesz syndrome,
+BMGC_DS08387,BMG_DS033628,722019000,Oculootoradial syndrome,,,,,DOID:0111381,IVIC syndrome,C1327918,C535544,147750,MONDO:0007836,IVIC syndrome,IVIC (Instituto Venezolano de Investigaciones Cientificas) syndrome | Oculootoradial syndrome (disorder) | Oculootoradial syndrome | Oculo-oto-radial syndrome | IVIC syndrome
+BMGC_DS08388,BMG_DS033629,,Myelocerebellar Disorder,,,,,,,C1327919,C563233,159550,MONDO:0008038,ataxia-pancytopenia syndrome,
+BMGC_DS08389,BMG_DS033630,,,,,,,DOID:3282,thymoma type B,C1328042,,,MONDO:0016974,thymoma type B,
+BMGC_DS08390,BMG_DS033632,721813000;39625001,Mucocutaneous leishmaniasis,,1F54.2,Mucocutaneous leishmaniasis,B55.2,DOID:9155,mucocutaneous leishmaniasis,C1328252,,,MONDO:0005859,mucocutaneous leishmaniasis,Mucocutaneous infection caused by Leishmania (disorder) | Mucocutaneous infection caused by Leishmania | Mucocutaneous leishmaniasis | Infection by Leishmania braziliensis | Espundia | Uta | Leishmania braziliensis complex | Infection caused by Leishmania braziliensis | Infection caused by Leishmania braziliensis (disorder)
+BMGC_DS08391,BMG_DS033635,,"Neuropathy, Ataxia, and Retinitis Pigmentosa",,,,,DOID:0111273,NARP syndrome,C1328349,C537396,551500,MONDO:0010794,NARP syndrome,
+BMGC_DS08392,BMG_DS033636,722675000,Laryngoonychocutaneous syndrome,,,,,,,C1328355,,245660,MONDO:0009513,laryngo-onycho-cutaneous syndrome,Laryngo-onycho-cutaneous syndrome (disorder) | Laryngo-onycho-cutaneous syndrome | LOC syndrome | LOGIC syndrome | Laryngoonychocutaneous syndrome | Shabbir syndrome
+BMGC_DS08393,BMG_DS033638,,,,,,,DOID:1625,breast adenoma,C1328385,,,MONDO:0002058,breast adenoma,
+BMGC_DS08394,BMG_DS033641,,,,,,,DOID:1798,pancreatic endocrine carcinoma,C1328479,,,MONDO:0005893,pancreatic endocrine carcinoma,
+BMGC_DS08395,BMG_DS033643,,,,,,,,,C1328504,,,MONDO:0850353,castration-resistant prostate carcinoma,
+BMGC_DS08396,BMG_DS033644,,,,,,,DOID:6587,breast tubular carcinoma,C1328544,,,MONDO:0003936,invasive tubular breast carcinoma,
+BMGC_DS08397,BMG_DS033645,426958002,Empty follicle syndrome,,,,,,,C1328577,,,,,Empty follicle syndrome (disorder) | Empty follicle syndrome
+BMGC_DS08398,BMG_DS033646,,Autoimmune Lymphoproliferative Syndrome,Autoimmune Lymphoproliferative Syndrome,,,,DOID:6688,autoimmune lymphoproliferative syndrome,C1328840,D056735,601859,MONDO:0017979;MONDO:0011158,autoimmune lymphoproliferative syndrome type 1 | autoimmune lymphoproliferative syndrome,
+BMGC_DS08399,BMG_DS033651,,,,,,,DOID:5438,extrahepatic bile duct adenoma,C1331534,,,MONDO:0003445,extrahepatic bile duct adenoma,
+BMGC_DS08400,BMG_DS033652,,,,,,,DOID:5437,intrahepatic bile duct adenoma,C1331535,,,MONDO:0003444,intrahepatic bile duct adenoma,
+BMGC_DS08401,BMG_DS033654,,,,,,,DOID:7350,thymic dysplasia,C1331541,,,MONDO:0004195,thymic dysplasia,
+BMGC_DS08402,BMG_DS033657,,,,,,,DOID:13160,scrotum melanoma,C1331544,,,MONDO:0001652,scrotum melanoma,
+BMGC_DS08403,BMG_DS033660,,,,,,,,,C1332079,,,MONDO:0017602,ALK-positive anaplastic large cell lymphoma,
+BMGC_DS08404,BMG_DS033661,,,,,,,DOID:9828,neonatal abstinence syndrome,C1332133,,,,,
+BMGC_DS08405,BMG_DS033662,,Achard syndrome,,,,,DOID:6686,Achard syndrome,C1332135,C536012,100700,MONDO:0007036,Achard syndrome,
+BMGC_DS08406,BMG_DS033663,,,,,,,DOID:6482,lung acinar adenocarcinoma,C1332137,,,MONDO:0003892,acinar lung adenocarcinoma,
+BMGC_DS08407,BMG_DS033664,,,,,,,DOID:3024,prostatic acinar adenocarcinoma,C1332139,,,MONDO:0002493,prostatic acinar adenocarcinoma,
+BMGC_DS08408,BMG_DS033665,,,,,,,DOID:5768,Nager acrofacial dysostosis,C1332140,,,MONDO:0018237,acrofacial dysostosis,
+BMGC_DS08409,BMG_DS033666,,,,,,,DOID:5224,acute hemorrhagic encephalitis,C1332149,,,MONDO:0003337,acute hemorrhagic encephalitis,
+BMGC_DS08410,BMG_DS033669,,,,,,,DOID:4877,breast adenoid cystic carcinoma,C1332167,,,MONDO:0003185,adenoid cystic breast carcinoma,
+BMGC_DS08411,BMG_DS033670,,,,,,,DOID:5626,thymus adenosquamous carcinoma,C1332171,,,MONDO:0003551,thymic adenosquamous carcinoma,
+BMGC_DS08412,BMG_DS033672,,,,,,,DOID:8140,adrenal gland ganglioneuroblastoma,C1332176,,,MONDO:0004477,adrenal gland ganglioneuroblastoma,
+BMGC_DS08413,BMG_DS033674,,,,,,,DOID:3076,adult astrocytic tumor,C1332183,,,MONDO:0002503,adult astrocytic tumor,
+BMGC_DS08414,BMG_DS033675,,,,,,,DOID:6847,adult botryoid rhabdomyosarcoma,C1332185,,,MONDO:0004012,adult botryoid rhabdomyosarcoma,
+BMGC_DS08415,BMG_DS033676,,,,,,,DOID:7750,adult brain ependymoma,C1332186,,,MONDO:0004352,adult brain ependymoma,
+BMGC_DS08416,BMG_DS033677,,,,,,,DOID:3186,adult oligodendroglioma,C1332190,,,,,
+BMGC_DS08417,BMG_DS033678,,,,,,,DOID:5922,adult brainstem astrocytoma,C1332191,,,MONDO:0003706,adult brainstem astrocytoma,
+BMGC_DS08418,BMG_DS033679,,,,,,,DOID:4203,brain stem cancer,C1332192,,,MONDO:0024797,adult brain stem neoplasm,
+BMGC_DS08419,BMG_DS033680,,,,,,,DOID:6018,adult central nervous system immature teratoma,C1332193,,,MONDO:0003734,adult central nervous system immature teratoma,
+BMGC_DS08420,BMG_DS033681,,,,,,,DOID:6016,adult central nervous system mature teratoma,C1332194,,,MONDO:0003732,adult central nervous system mature teratoma,
+BMGC_DS08421,BMG_DS033682,,,,,,,DOID:7945,adult central nervous system mixed germ cell tumor,C1332195,,,MONDO:0004406,adult central nervous system mixed germ cell tumor,
+BMGC_DS08422,BMG_DS033684,,,,,,,DOID:5056,adult cerebellar neoplasm,C1332197,,,MONDO:0003260,adult cerebellar neoplasm,
+BMGC_DS08423,BMG_DS033685,,,,,,,DOID:4233,clear cell sarcoma,C1332198,,,,,
+BMGC_DS08424,BMG_DS033687,,,,,,,DOID:6090,adult leptomeningeal melanoma,C1332204,,,MONDO:0003765,adult leptomeningeal melanoma,
+BMGC_DS08425,BMG_DS033688,,,,,,,DOID:5825,adult lymphoma,C1332206,,,MONDO:0003660,adult lymphoma,
+BMGC_DS08426,BMG_DS033689,,,,,,,DOID:4547,adult mesenchymal chondrosarcoma,C1332207,,,MONDO:0003042,adult mesenchymal chondrosarcoma,
+BMGC_DS08427,BMG_DS033691,,,,,,,DOID:8251,adult pleomorphic rhabdomyosarcoma,C1332211,,,MONDO:0004513,adult pleomorphic rhabdomyosarcoma,
+BMGC_DS08428,BMG_DS033692,,,,,,,DOID:7788,adult spinal cord ependymoma,C1332215,,,MONDO:0004361,adult spinal cord ependymoma,
+BMGC_DS08429,BMG_DS033693,,,,,,,DOID:2154,nephroblastoma,C1332219,,,MONDO:0024675,adult kidney Wilms tumor,
+BMGC_DS08430,BMG_DS033694,,,,,,,DOID:7875,adult xanthogranuloma,C1332220,,,MONDO:0004385,adult xanthogranuloma,
+BMGC_DS08431,BMG_DS033695,,,,,,,DOID:5348,adult endodermal sinus tumor,C1332221,,,MONDO:0003404,adult yolk sac tumor,
+BMGC_DS08432,BMG_DS033696,,,,,,,DOID:5022,aflatoxins-related hepatocellular carcinoma,C1332222,,,MONDO:0003245,aflatoxin-related hepatocellular carcinoma,
+BMGC_DS08433,BMG_DS033697,,,,,,,DOID:6958,aleukemic monocytic leukemia cutis,C1332232,,,MONDO:0004051,aleukemic monocytic leukemia cutis,
+BMGC_DS08434,BMG_DS033699,,,,,,,DOID:3502,ampulla of Vater adenocarcinoma,C1332243,,,MONDO:0002670,ampulla of vater adenocarcinoma,
+BMGC_DS08435,BMG_DS033700,,,,,,,DOID:5628,ampulla of Vater adenosquamous carcinoma,C1332245,,,MONDO:0003553,ampulla of vater adenosquamous carcinoma,
+BMGC_DS08436,BMG_DS033701,,,,,,,DOID:5308,ampulla of Vater clear cell adenocarcinoma,C1332246,,,MONDO:0003388,ampulla of vater clear cell adenocarcinoma,
+BMGC_DS08437,BMG_DS033702,,,,,,,DOID:3693,ampulla of Vater mucinous adenocarcinoma,C1332248,,,MONDO:0002736,ampulla of vater mucinous adenocarcinoma,
+BMGC_DS08438,BMG_DS033703,,,,,,,DOID:3501,ampullary signet ring cell adenocarcinoma,C1332249,,,MONDO:0002669,ampullary signet ring cell adenocarcinoma,
+BMGC_DS08439,BMG_DS033704,,,,,,,DOID:7136,ampulla of Vater small cell carcinoma,C1332250,,,MONDO:0004117,ampulla of vater small cell neuroendocrine carcinoma,
+BMGC_DS08440,BMG_DS033705,,,,,,,DOID:5527,ampulla of Vater squamous cell carcinoma,C1332251,,,MONDO:0003490,ampulla of vater squamous cell carcinoma,
+BMGC_DS08441,BMG_DS033706,,,,,,,DOID:3447,anus adenocarcinoma,C1332257,,,MONDO:0002652,anus adenocarcinoma,
+BMGC_DS08442,BMG_DS033707,,,,,,,DOID:3692,anal canal adenocarcinoma,C1332259,,,MONDO:0002735,anal canal adenocarcinoma,
+BMGC_DS08443,BMG_DS033708,,,,,,,DOID:8119,anal canal Paget's disease,C1332261,,,MONDO:0004468,anal canal Paget disease,
+BMGC_DS08444,BMG_DS033710,,,,,,,DOID:8632,Kaposi's sarcoma,C1332265,,,,,
+BMGC_DS08445,BMG_DS033712,,,,,,,DOID:5267,anus leiomyosarcoma,C1332267,,,MONDO:0003358,anus leiomyosarcoma,
+BMGC_DS08446,BMG_DS033713,,,,,,,DOID:14139,anus lymphoma,C1332268,,,MONDO:0001888,anus lymphoma,
+BMGC_DS08447,BMG_DS033714,,,,,,,DOID:4283,anal margin basal cell carcinoma,C1332269,,,MONDO:0002940,anal margin basal cell carcinoma,
+BMGC_DS08448,BMG_DS033715,,,,,,,DOID:7708,perianal skin Paget's disease,C1332270,,,MONDO:0004337,perianal skin Paget disease,
+BMGC_DS08449,BMG_DS033716,,,,,,,DOID:3691,anal colloid adenocarcinoma,C1332272,,,MONDO:0002734,anal mucinous adenocarcinoma,
+BMGC_DS08450,BMG_DS033717,,,,,,,DOID:5545,anal neuroendocrine tumor,C1332273,,,MONDO:0003504,anal canal neuroendocrine neoplasm,
+BMGC_DS08451,BMG_DS033718,,,,,,,DOID:3446,anal Paget's disease,C1332274,,,MONDO:0002651,anal Paget disease,
+BMGC_DS08452,BMG_DS033719,,,,,,,DOID:4066,anus rhabdomyosarcoma,C1332276,,,MONDO:0002864,anus rhabdomyosarcoma,
+BMGC_DS08453,BMG_DS033720,,,,,,,DOID:4067,anus sarcoma,C1332277,,,MONDO:0002865,anus sarcoma,
+BMGC_DS08454,BMG_DS033721,,,,,,,DOID:7175,anal Buschke-Lowenstein tumor,C1332278,,,MONDO:0004131,anal verrucous carcinoma,
+BMGC_DS08455,BMG_DS033723,,,,,,,DOID:4436,anterior cranial fossa meningioma,C1332301,,,MONDO:0002997,anterior cranial fossa meningioma,
+BMGC_DS08456,BMG_DS033724,,,,,,,DOID:6381,anterior foramen magnum meningioma,C1332302,,,MONDO:0003868,anterior foramen magnum meningioma,
+BMGC_DS08457,BMG_DS033725,,,,,,,DOID:6334,anterior optic tract meningioma,C1332308,,,MONDO:0003858,anterior optic tract meningioma,
+BMGC_DS08458,BMG_DS033726,,,,,,,DOID:4780,anti-basement membrane glomerulonephritis,C1332309,,,MONDO:0003136,anti-basement membrane glomerulonephritis,
+BMGC_DS08459,BMG_DS033727,,,,,,,DOID:4510,aorta angiosarcoma,C1332312,,,MONDO:0003023,aorta angiosarcoma,
+BMGC_DS08460,BMG_DS033728,,,,,,,DOID:5999,apocrine adenosis of breast,C1332314,,,MONDO:0003726,apocrine adenosis of breast,
+BMGC_DS08461,BMG_DS033729,,,,,,,DOID:8428,breast apocrine carcinoma in situ,C1332315,,,MONDO:0004562,breast apocrine carcinoma in situ,
+BMGC_DS08462,BMG_DS033730,,,,,,,DOID:6581,breast apocrine carcinoma,C1332316,,,MONDO:0003934,breast apocrine carcinoma,
+BMGC_DS08463,BMG_DS033731,,,,,,,DOID:5876,apocrine sweat gland neoplasm,C1332318,,,MONDO:0003686,apocrine sweat gland neoplasm,
+BMGC_DS08464,BMG_DS033733,,,,,,,DOID:11241,appendix lymphoma,C1332328,,,MONDO:0001237,appendix lymphoma,
+BMGC_DS08465,BMG_DS033735,,,,,,,DOID:7596,asbestos-related lung carcinoma,C1332337,,,MONDO:0004295,asbestos-related lung carcinoma,
+BMGC_DS08466,BMG_DS033736,,,,,,,DOID:1790,malignant mesothelioma,C1332338,,,,,
+BMGC_DS08467,BMG_DS033738,,,,,,,DOID:7559,asymmetric motor neuropathy,C1332341,,,MONDO:0004280,asymmetric motor neuropathy,
+BMGC_DS08468,BMG_DS033739,,,,,,,DOID:6697,asynchronous multifocal osteogenic sarcoma,C1332342,,,MONDO:0003968,asynchronous multifocal osteogenic sarcoma,
+BMGC_DS08469,BMG_DS033740,,,,,,,DOID:8227,atypical breast papilloma,C1332346,,,MONDO:0004507,atypical breast papilloma,
+BMGC_DS08470,BMG_DS033741,,,,,,,DOID:2048,autoimmune hepatitis,C1332355,,,,,
+BMGC_DS08471,BMG_DS033742,,,,,,,DOID:2621,autonomic nervous system neoplasm,C1332356,,,MONDO:0002366,autonomic nervous system neoplasm,
+BMGC_DS08472,BMG_DS033743,,,,,,,DOID:7941,Barrett's adenocarcinoma,C1332460,,,MONDO:0004405,Barrett adenocarcinoma,
+BMGC_DS08473,BMG_DS033744,,,,,,,DOID:7047,penis basaloid carcinoma,C1332462,,,MONDO:0004089,basaloid carcinoma of the penis,
+BMGC_DS08474,BMG_DS033745,,,,,,,DOID:7045,basaloid lung carcinoma,C1332463,,,MONDO:0004087,basaloid large cell lung carcinoma,
+BMGC_DS08475,BMG_DS033746,,,,,,,DOID:7050,thymus basaloid carcinoma,C1332464,,,MONDO:0004092,thymic basaloid carcinoma,
+BMGC_DS08476,BMG_DS033748,,,,,,,DOID:7181,benign dermal neurilemmoma,C1332490,,,MONDO:0004134,benign dermal neurilemmoma,
+BMGC_DS08477,BMG_DS033752,,,,,,,DOID:7921,mediastinal psammomatous neurilemmoma,C1332513,,,MONDO:0004397,benign mediastinal psammomatous neurilemmoma,
+BMGC_DS08478,BMG_DS033753,,,,,,,DOID:3350,mesenchymal cell neoplasm,C1332517,,,,,
+BMGC_DS08479,BMG_DS033757,,,,,,,DOID:5238,benign perivascular tumor,C1332532,,,MONDO:0003342,benign perivascular tumor,
+BMGC_DS08480,BMG_DS033763,,,,,,,DOID:6335,bilateral meningioma of optic nerve,C1332551,,,MONDO:0003859,bilateral meningioma of optic nerve,
+BMGC_DS08481,BMG_DS033764,,,,,,,DOID:4681,bile duct mucoepidermoid carcinoma,C1332552,,,MONDO:0003089,extrahepatic bile duct mucoepidermoid carcinoma,
+BMGC_DS08482,BMG_DS033765,,,,,,,DOID:4767,classic pulmonary blastoma,C1332556,,,MONDO:0003128,classic pulmonary blastoma,
+BMGC_DS08483,BMG_DS033766,,,,,,,DOID:5306,bladder clear cell adenocarcinoma,C1332557,,,MONDO:0003386,bladder clear cell adenocarcinoma,
+BMGC_DS08484,BMG_DS033769,,,,,,,DOID:11821,bladder lymphoma,C1332561,,,MONDO:0001381,bladder lymphoma,
+BMGC_DS08485,BMG_DS033770,,,,,,,DOID:6481,bladder signet ring cell adenocarcinoma,C1332563,,,MONDO:0003891,bladder signet ring cell adenocarcinoma,
+BMGC_DS08486,BMG_DS033771,,,,,,,DOID:7132,urinary bladder small cell neuroendocrine carcinoma,C1332564,,,MONDO:0004114,urinary bladder small cell neuroendocrine carcinoma,
+BMGC_DS08487,BMG_DS033775,,,,,,,DOID:3367,bone leiomyosarcoma,C1332579,,,MONDO:0002624,bone leiomyosarcoma,
+BMGC_DS08488,BMG_DS033776,,,,,,,DOID:3381,liposarcoma of bone,C1332581,,,MONDO:0002634,liposarcoma of bone,
+BMGC_DS08489,BMG_DS033777,,,,,,,DOID:6759,bone lymphoma,C1332582,,,MONDO:0017814,primary bone lymphoma,
+BMGC_DS08490,BMG_DS033778,,,,,,,DOID:3374,peripheral osteosarcoma,C1332591,,,MONDO:0002628,peripheral osteosarcoma,
+BMGC_DS08491,BMG_DS033780,,,,,,,DOID:5913,brachial plexus neoplasm,C1332602,,,MONDO:0003700,brachial plexus neoplasm,
+BMGC_DS08492,BMG_DS033781,,,,,,,DOID:2127,brain germinoma,C1332606,,,MONDO:0002214,brain germinoma,
+BMGC_DS08493,BMG_DS033782,,,,,,,DOID:2132,brain sarcoma,C1332607,,,MONDO:0002216,brain sarcoma,
+BMGC_DS08494,BMG_DS033783,,,,,,,DOID:4860,brain stem astrocytic neoplasm,C1332608,,,MONDO:0003173,brain stem astrocytic neoplasm,
+BMGC_DS08495,BMG_DS033784,,,,,,,DOID:5508,brain stem ependymoma,C1332609,,,MONDO:0003477,brain stem ependymoma,
+BMGC_DS08496,BMG_DS033785,,,,,,,DOID:6501,brain stem angioblastoma,C1332611,,,MONDO:0003902,brain stem hemangioblastoma,
+BMGC_DS08497,BMG_DS033786,,,,,,,DOID:4209,brainstem intraparenchymal clear cell meningioma,C1332612,,,MONDO:0002916,brainstem intraparenchymal clear cell meningioma,
+BMGC_DS08498,BMG_DS033787,,,,,,,DOID:4511,breast angiosarcoma,C1332614,,,MONDO:0003024,breast angiosarcoma,
+BMGC_DS08499,BMG_DS033788,,,,,,,DOID:6491,breast capillary hemangioma,C1332619,,,MONDO:0003896,breast capillary hemangioma,
+BMGC_DS08500,BMG_DS033789,,,,,,,DOID:6492,breast epithelioid hemangioma,C1332627,,,MONDO:0003897,breast epithelioid hemangioma,
+BMGC_DS08501,BMG_DS033790,,,,,,,DOID:5997,non-proliferative fibrocystic change of the breast,C1332628,,,MONDO:0003724,non-proliferative fibrocystic change of the breast,
+BMGC_DS08502,BMG_DS033792,,,,,,,DOID:6001,breast fibrosarcoma,C1332630,,,MONDO:0003728,breast fibrosarcoma,
+BMGC_DS08503,BMG_DS033793,,,,,,,DOID:5285,breast leiomyosarcoma,C1332631,,,MONDO:0003371,breast leiomyosarcoma,
+BMGC_DS08504,BMG_DS033794,,,,,,,DOID:5701,breast liposarcoma,C1332632,,,MONDO:0003593,breast liposarcoma,
+BMGC_DS08505,BMG_DS033797,,,,,,,DOID:4060,breast rhabdomyosarcoma,C1332637,,,MONDO:0002859,breast rhabdomyosarcoma,
+BMGC_DS08506,BMG_DS033798,,,,,,,DOID:7030,bronchial mucus gland adenoma,C1332640,,,MONDO:0004079,lung mucous gland adenoma,
+BMGC_DS08507,BMG_DS033800,771443008,Complement component 3 deficiency,,,,,DOID:8354,complement component 3 deficiency,C1332655,,,,,Complement component 3 deficiency | Complement component 3 deficiency (disorder) | C3 deficiency
+BMGC_DS08508,BMG_DS033802,,,,,,,DOID:8415,carcinoma arising in nasal papillomatosis,C1332840,,,MONDO:0004556,carcinoma arising in nasal papillomatosis,
+BMGC_DS08509,BMG_DS033803,,,,,,,DOID:6033,heart fibrosarcoma,C1332844,,,MONDO:0003742,heart fibrosarcoma,
+BMGC_DS08510,BMG_DS033805,,,,,,,DOID:8632,Kaposi's sarcoma,C1332847,,,,,
+BMGC_DS08511,BMG_DS033806,,,,,,,DOID:5261,heart leiomyosarcoma,C1332848,,,MONDO:0003353,heart leiomyosarcoma,
+BMGC_DS08512,BMG_DS033807,,,,,,,DOID:6285,heart lipoma,C1332849,,,MONDO:0003841,heart lipoma,
+BMGC_DS08513,BMG_DS033808,,,,,,,DOID:6547,heart lymphoma,C1332850,,,MONDO:0003917,heart lymphoma,
+BMGC_DS08514,BMG_DS033809,,,,,,,,,C1332852,,,MONDO:0006123,cardiac rhabdomyoma,
+BMGC_DS08515,BMG_DS033811,,,,,,,DOID:5776,cavernous hemangioma of face,C1332863,,,MONDO:0003645,cavernous hemangioma of face,
+BMGC_DS08516,BMG_DS033812,,,,,,,DOID:4435,cavernous sinus meningioma,C1332865,,,MONDO:0002996,cavernous sinus meningioma,
+BMGC_DS08517,BMG_DS033813,,,,,,,DOID:3039,cecum adenocarcinoma,C1332866,,,MONDO:0006028,cecum adenocarcinoma,
+BMGC_DS08518,BMG_DS033814,,,,,,,DOID:1522,cecum lymphoma,C1332867,,,MONDO:0002034,cecum lymphoma,
+BMGC_DS08519,BMG_DS033816,,,,,,,DOID:4504,central nervous system angiosarcoma,C1332875,,,MONDO:0003021,central nervous system angiosarcoma,
+BMGC_DS08520,BMG_DS033818,,,,,,,DOID:6451,central nervous system fibrosarcoma,C1332879,,,MONDO:0003882,central nervous system fibrosarcoma,
+BMGC_DS08521,BMG_DS033819,,,,,,,DOID:4439,central nervous system germ cell tumor,C1332880,,,MONDO:0003000,central nervous system germ cell tumor,
+BMGC_DS08522,BMG_DS033820,,,,,,,DOID:5772,central nervous system hematologic cancer,C1332882,,,MONDO:0003641,central nervous system hematopoietic neoplasm,
+BMGC_DS08523,BMG_DS033821,,,,,,,DOID:6019,central nervous system immature teratoma,C1332883,,,MONDO:0003735,central nervous system immature teratoma,
+BMGC_DS08524,BMG_DS033822,,,,,,,DOID:12969,central nervous system leukemia,C1332884,,,MONDO:0001606,central nervous system leukemia,
+BMGC_DS08525,BMG_DS033823,,,,,,,DOID:6293,central nervous system lipoma,C1332885,,,MONDO:0003844,central nervous system lipoma,
+BMGC_DS08526,BMG_DS033824,,,,,,,DOID:6017,central nervous system mature teratoma,C1332886,,,MONDO:0003733,central nervous system mature teratoma,
+BMGC_DS08527,BMG_DS033825,,,,,,,DOID:4955,central nervous system melanocytic neoplasm,C1332887,,,MONDO:0003222,central nervous system melanocytic neoplasm,
+BMGC_DS08528,BMG_DS033826,,,,,,,DOID:4048,central nervous system rhabdomyosarcoma,C1332891,,,MONDO:0002850,central nervous system rhabdomyosarcoma,
+BMGC_DS08529,BMG_DS033827,,,,,,,DOID:2133,central nervous system sarcoma,C1332892,,,MONDO:0002217,central nervous system sarcoma,
+BMGC_DS08530,BMG_DS033829,,,,,,,DOID:3640,central nervous system teratoma,C1332895,,,MONDO:0002718,central nervous system teratoma,
+BMGC_DS08531,BMG_DS033830,,,,,,,DOID:8224,central breast papilloma,C1332896,,,MONDO:0004505,central breast papilloma,
+BMGC_DS08532,BMG_DS033831,,,,,,,DOID:6500,cerebellar angioblastoma,C1332900,,,MONDO:0003901,cerebellar hemangioblastoma,
+BMGC_DS08533,BMG_DS033832,,,,,,,DOID:5057,papillary meningioma of the cerebellum,C1332902,,,MONDO:0003261,papillary meningioma of the cerebellum,
+BMGC_DS08534,BMG_DS033836,,,,,,,DOID:6291,cerebral hemisphere lipoma,C1332907,,,MONDO:0003843,cerebral hemisphere lipoma,
+BMGC_DS08535,BMG_DS033837,,,,,,,DOID:4867,cervical adenoid cystic carcinoma,C1332911,,,MONDO:0006133,cervical adenoid cystic carcinoma,
+BMGC_DS08536,BMG_DS033838,,,,,,,DOID:5303,cervical clear cell adenocarcinoma,C1332912,,,MONDO:0006135,cervical clear cell adenocarcinoma,
+BMGC_DS08537,BMG_DS033839,,,,,,,DOID:5830,cervical endometrioid adenocarcinoma,C1332913,,,MONDO:0003665,cervical endometrioid adenocarcinoma,
+BMGC_DS08538,BMG_DS033840,,,,,,,DOID:7915,cervical spinal canal and spinal cord meningioma,C1332916,,,MONDO:0004396,cervical spinal canal and spinal cord meningioma,
+BMGC_DS08539,BMG_DS033841,,,,,,,DOID:4112,cervical carcinosarcoma,C1332917,,,MONDO:0002877,cervical carcinosarcoma,
+BMGC_DS08540,BMG_DS033842,,,,,,,DOID:3701,cervical mucinous adenocarcinoma,C1332919,,,MONDO:0002742,cervical mucinous adenocarcinoma,
+BMGC_DS08541,BMG_DS033844,,,,,,,DOID:4707,cervicomedullary junction neoplasm,C1332923,,,MONDO:0003108,cervicomedullary junction neoplasm,
+BMGC_DS08542,BMG_DS033846,,,,,,,DOID:6758,chest wall lymphoma,C1332933,,,MONDO:0003985,chest wall lymphoma,
+BMGC_DS08543,BMG_DS033847,,,,,,,DOID:8043,chest wall parachordoma,C1332934,,,MONDO:0004443,chest wall parachordoma,
+BMGC_DS08544,BMG_DS033848,,,,,,,DOID:3723,solitary plasmacytoma of chest wall,C1332936,,,MONDO:0002756,solitary plasmacytoma of chest wall,
+BMGC_DS08545,BMG_DS033849,,,,,,,DOID:6786,childhood botryoid rhabdomyosarcoma,C1332944,,,MONDO:0003992,childhood botryoid rhabdomyosarcoma,
+BMGC_DS08546,BMG_DS033850,,,,,,,DOID:6787,childhood vagina botryoid rhabdomyosarcoma,C1332945,,,MONDO:0003993,childhood vagina botryoid rhabdomyosarcoma,
+BMGC_DS08547,BMG_DS033851,,,,,,,DOID:6789,vulvar childhood botryoid-type embryonal rhabdomyosarcoma,C1332946,,,MONDO:0003995,vulvar childhood botryoid-type embryonal rhabdomyosarcoma,
+BMGC_DS08548,BMG_DS033852,,,,,,,DOID:7429,childhood brain germinoma,C1332948,,,MONDO:0004217,childhood brain germinoma,
+BMGC_DS08549,BMG_DS033854,,,,,,,DOID:6386,childhood brainstem astrocytoma,C1332950,,,MONDO:0003870,childhood brainstem astrocytoma,
+BMGC_DS08550,BMG_DS033855,,,,,,,DOID:4206,childhood brain stem neoplasm,C1332951,,,MONDO:0002914,childhood brain stem neoplasm,
+BMGC_DS08551,BMG_DS033856,,,,,,,DOID:8078,childhood central nervous system germinoma,C1332953,,,MONDO:0004452,childhood central nervous system germinoma,
+BMGC_DS08552,BMG_DS033857,,,,,,,DOID:6654,childhood central nervous system immature teratoma,C1332954,,,MONDO:0003958,childhood central nervous system immature teratoma,
+BMGC_DS08553,BMG_DS033858,,,,,,,DOID:6423,childhood central nervous system mature teratoma,C1332955,,,MONDO:0003875,childhood central nervous system mature teratoma,
+BMGC_DS08554,BMG_DS033859,,,,,,,DOID:7516,childhood central nervous system mixed germ cell tumor,C1332956,,,MONDO:0004257,childhood central nervous system mixed germ cell tumor,
+BMGC_DS08555,BMG_DS033861,,,,,,,DOID:5059,childhood cerebellar neoplasm,C1332959,,,MONDO:0003263,childhood cerebellar neoplasm,
+BMGC_DS08556,BMG_DS033864,,,,,,,DOID:4773,congenital mesoblastic nephroma,C1332965,,,MONDO:0017043,congenital mesoblastic nephroma,
+BMGC_DS08557,BMG_DS033865,,,,,,,DOID:7297,childhood extraosseous osteosarcoma,C1332968,,,MONDO:0004176,childhood extraosseous osteosarcoma,
+BMGC_DS08558,BMG_DS033867,,,,,,,DOID:7522,"childhood infratentorial embryonal tumor with multilayered rosettes, C19MC-altered",C1332972,,,MONDO:0004263,pediatric infratentorial ependymoblastoma,
+BMGC_DS08559,BMG_DS033868,,,,,,,DOID:4207,childhood infratentorial neoplasm,C1332973,,,MONDO:0002915,childhood infratentorial neoplasm,
+BMGC_DS08560,BMG_DS033869,,,,,,,DOID:7612,childhood intracortical osteosarcoma,C1332974,,,MONDO:0004306,childhood intracortical osteosarcoma,
+BMGC_DS08561,BMG_DS033870,,,,,,,DOID:6089,childhood leptomeningeal melanoma,C1332976,,,MONDO:0003764,pediatric leptomeningeal melanoma,
+BMGC_DS08562,BMG_DS033871,,,,,,,DOID:7757,childhood leukemia,C1332977,,,MONDO:0004355,childhood leukemia,
+BMGC_DS08563,BMG_DS033872,,,,,,,DOID:5823,childhood lymphoma,C1332979,,,MONDO:0003659,pediatric lymphoma,
+BMGC_DS08564,BMG_DS033873,,,,,,,DOID:4690,childhood mediastinal neurogenic tumor,C1332981,,,MONDO:0003097,childhood mediastinal neurogenic neoplasm,
+BMGC_DS08565,BMG_DS033874,,,,,,,DOID:4546,childhood mesenchymal chondrosarcoma,C1332982,,,MONDO:0003041,pediatric mesenchymal chondrosarcoma,
+BMGC_DS08566,BMG_DS033875,,,,,,,DOID:7762,childhood multilocular cystic kidney neoplasm,C1332983,,,MONDO:0004356,childhood multilocular cystic kidney neoplasm,
+BMGC_DS08567,BMG_DS033876,,,,,,,DOID:6494,childhood myxoid chondrosarcoma,C1332984,,,MONDO:0003898,pediatric myxoid chondrosarcoma,
+BMGC_DS08568,BMG_DS033877,,,,,,,DOID:3361,childhood osteosarcoma,C1332986,,,MONDO:0002623,pediatric osteosarcoma,
+BMGC_DS08569,BMG_DS033878,,,,,,,DOID:8336,childhood choriocarcinoma of the ovary,C1332987,,,MONDO:0004535,childhood choriocarcinoma of the ovary,
+BMGC_DS08570,BMG_DS033879,,,,,,,DOID:7340,childhood ovarian dysgerminoma,C1332988,,,MONDO:0004193,pediatric ovarian dysgerminoma,
+BMGC_DS08571,BMG_DS033880,,,,,,,DOID:8036,childhood ovarian embryonal carcinoma,C1332989,,,MONDO:0004441,childhood ovarian embryonal carcinoma,
+BMGC_DS08572,BMG_DS033881,,,,,,,DOID:7037,childhood immature teratoma of ovary,C1332990,,,MONDO:0004082,childhood immature teratoma of ovary,
+BMGC_DS08573,BMG_DS033882,,,,,,,DOID:6229,childhood mature teratoma of the ovary,C1332991,,,MONDO:0003818,childhood mature teratoma of the ovary,
+BMGC_DS08574,BMG_DS033883,,,,,,,DOID:6230,childhood teratoma of the ovary,C1332992,,,MONDO:0003819,childhood teratoma of the ovary,
+BMGC_DS08575,BMG_DS033884,,,,,,,DOID:6083,childhood ovarian endodermal sinus tumor,C1332993,,,MONDO:0003759,childhood ovarian yolk sac tumor,
+BMGC_DS08576,BMG_DS033885,,,,,,,DOID:5809,childhood parosteal osteogenic sarcoma,C1332994,,,MONDO:0003654,childhood parosteal osteosarcoma,
+BMGC_DS08577,BMG_DS033886,,,,,,,DOID:6812,childhood pilocytic astrocytoma,C1332995,,,MONDO:0004000,childhood pilocytic astrocytoma,
+BMGC_DS08578,BMG_DS033889,,,,,,,DOID:8410,childhood kidney angiomyolipoma,C1333000,,,MONDO:0004554,childhood kidney angiomyolipoma,
+BMGC_DS08579,BMG_DS033890,,,,,,,DOID:4454,childhood kidney cell carcinoma,C1333001,,,MONDO:0003007,childhood kidney cell carcinoma,
+BMGC_DS08580,BMG_DS033891,,,,,,,DOID:3675,childhood kidney cancer,C1333003,,,MONDO:0002730,childhood kidney neoplasm,
+BMGC_DS08581,BMG_DS033892,,,,,,,DOID:6160,childhood choriocarcinoma of the testis,C1333006,,,MONDO:0003786,childhood testicular choriocarcinoma,
+BMGC_DS08582,BMG_DS033893,,,,,,,DOID:6162,childhood embryonal testis carcinoma,C1333007,,,MONDO:0003788,childhood embryonal testis carcinoma,
+BMGC_DS08583,BMG_DS033894,,,,,,,DOID:6474,childhood teratocarcinoma of the testis,C1333008,,,MONDO:0003888,childhood testicular mixed embryonal carcinoma and teratoma,
+BMGC_DS08584,BMG_DS033895,,,,,,,DOID:6161,childhood testicular mixed germ cell tumor,C1333009,,,MONDO:0003787,childhood testicular mixed germ cell cancer,
+BMGC_DS08585,BMG_DS033896,,,,,,,DOID:2998,testicular cancer,C1333010,,,MONDO:0037250,childhood testicular neoplasm,
+BMGC_DS08586,BMG_DS033897,,,,,,,DOID:6575,childhood optic tract astrocytoma,C1333014,,,MONDO:0003931,childhood optic tract astrocytoma,
+BMGC_DS08587,BMG_DS033898,,,,,,,DOID:2154,nephroblastoma,C1333015,,,MONDO:0024676,childhood kidney Wilms tumor,
+BMGC_DS08588,BMG_DS033899,,,,,,,DOID:5342,childhood endodermal sinus tumor,C1333016,,,MONDO:0003400,childhood endodermal sinus tumor,
+BMGC_DS08589,BMG_DS033901,,,,,,,DOID:7041,choroid epithelioid cell melanoma,C1333024,,,MONDO:0004085,choroid epithelioid cell melanoma,
+BMGC_DS08590,BMG_DS033902,,,,,,,DOID:6525,choroid mixed cell melanoma,C1333025,,,MONDO:0003913,choroid mixed cell melanoma,
+BMGC_DS08591,BMG_DS033903,,,,,,,DOID:7807,choroid necrotic melanoma,C1333026,,,MONDO:0004364,choroid necrotic melanoma,
+BMGC_DS08592,BMG_DS033904,,,,,,,DOID:6041,choroid spindle cell melanoma,C1333027,,,MONDO:0003745,choroid spindle cell melanoma,
+BMGC_DS08593,BMG_DS033905,,,,,,,DOID:7230,postgerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma,C1333037,,,MONDO:0004152,chronic lymphocytic leukemia/small lymphocytic lymphoma with immunoglobulin heavy chain variable-region gene somatic hypermutation,
+BMGC_DS08594,BMG_DS033906,,,,,,,DOID:8144,pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma,C1333038,,,MONDO:0004478,pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma,
+BMGC_DS08595,BMG_DS033907,,,,,,,DOID:7441,chronic metabolic polyneuropathy,C1333042,,,MONDO:0004224,chronic metabolic polyneuropathy,
+BMGC_DS08596,BMG_DS033908,,,,,,,,,C1333046,,,MONDO:0019452,"myeloproliferative neoplasm, unclassifiable",
+BMGC_DS08597,BMG_DS033909,,,,,,,DOID:7825,chronic toxic polyneuropathy,C1333048,,,MONDO:0004372,chronic toxic polyneuropathy,
+BMGC_DS08598,BMG_DS033910,,,,,,,DOID:7042,ciliary body epithelioid cell melanoma,C1333050,,,MONDO:0004086,ciliary body epithelioid cell melanoma,
+BMGC_DS08599,BMG_DS033911,,,,,,,DOID:6523,ciliary body mixed cell melanoma,C1333051,,,MONDO:0003911,ciliary body mixed cell melanoma,
+BMGC_DS08600,BMG_DS033912,,,,,,,DOID:6043,ciliary body spindle cell melanoma,C1333052,,,MONDO:0003746,ciliary body spindle cell melanoma,
+BMGC_DS08601,BMG_DS033913,,,,,,,DOID:10193,conventional lipoma,C1333059,,,MONDO:0000967,conventional lipoma,
+BMGC_DS08602,BMG_DS033914,,,,,,,DOID:6605,classic variant of chromophobe renal cell carcinoma,C1333062,,,MONDO:0003941,classic variant of chromophobe renal cell carcinoma,
+BMGC_DS08603,BMG_DS033915,,,,,,,DOID:5763,lung clear cell-sugar-tumor,C1333065,,,MONDO:0003637,clear cell-sugar-tumor of the lung,
+BMGC_DS08604,BMG_DS033916,,,,,,,DOID:8137,thymus clear cell carcinoma,C1333069,,,MONDO:0004475,thymus clear cell carcinoma,
+BMGC_DS08605,BMG_DS033917,,,,,,,DOID:2401,clitoris cancer,C1333070,,,MONDO:0024873,clitoral carcinoma,
+BMGC_DS08606,BMG_DS033918,,,,,,,DOID:6312,clivus chordoma,C1333071,,,MONDO:0003849,clivus chordoma,
+BMGC_DS08607,BMG_DS033919,,,,,,,DOID:6313,clivus chondroid chordoma,C1333072,,,MONDO:0003850,clivus chondroid chordoma,
+BMGC_DS08608,BMG_DS033920,,,,,,,DOID:6517,clivus meningioma,C1333073,,,MONDO:0003908,clivus meningioma,
+BMGC_DS08609,BMG_DS033921,,,,,,,DOID:6959,rectal cloacogenic carcinoma,C1333074,,,MONDO:0004052,rectal cloacogenic carcinoma,
+BMGC_DS08610,BMG_DS033922,,,,,,,DOID:7717,colloid carcinoma of the pancreas,C1333081,,,MONDO:0004341,colloid carcinoma of the pancreas,
+BMGC_DS08611,BMG_DS033923,,,,,,,DOID:5629,adenosquamous colon carcinoma,C1333082,,,MONDO:0003554,adenosquamous colon carcinoma,
+BMGC_DS08612,BMG_DS033926,,,,,,,DOID:5775,cavernous hemangioma of colon,C1333086,,,MONDO:0003644,cavernous hemangioma of colon,
+BMGC_DS08613,BMG_DS033928,,,,,,,DOID:6804,colon Kaposi sarcoma,C1333091,,,MONDO:0003997,colon Kaposi sarcoma,
+BMGC_DS08614,BMG_DS033929,,,,,,,DOID:10656,colon leiomyoma,C1333092,,,MONDO:0001092,colon leiomyoma,
+BMGC_DS08615,BMG_DS033930,,,,,,,DOID:5259,colon leiomyosarcoma,C1333093,,,MONDO:0003351,colon leiomyosarcoma,
+BMGC_DS08616,BMG_DS033931,,,,,,,DOID:10657,colonic lymphangioma,C1333094,,,MONDO:0001093,colonic lymphangioma,
+BMGC_DS08617,BMG_DS033933,,,,,,,DOID:4118,colon neuroendocrine neoplasm,C1333097,,,MONDO:0002882,colon neuroendocrine neoplasm,
+BMGC_DS08618,BMG_DS033934,,,,,,,DOID:5260,colon sarcoma,C1333098,,,MONDO:0003352,colon sarcoma,
+BMGC_DS08619,BMG_DS033935,,,,,,,DOID:6727,colon small cell carcinoma,C1333099,,,MONDO:0003978,colon small cell neuroendocrine carcinoma,
+BMGC_DS08620,BMG_DS033936,,,,,,,DOID:5519,colon squamous cell carcinoma,C1333100,,,MONDO:0018513,squamous cell carcinoma of colon,
+BMGC_DS08621,BMG_DS033938,,,,,,,DOID:5143,large bowel leiomyoma,C1333113,,,MONDO:0003299,colorectal leiomyoma,
+BMGC_DS08622,BMG_DS033939,,,,,,,DOID:6460,large intestine lipoma,C1333114,,,MONDO:0003885,colorectal lipoma,
+BMGC_DS08623,BMG_DS033941,,,,,,,DOID:7088,columnar cell papillary thyroid carcinoma,C1333120,,,MONDO:0004102,columnar cell variant thyroid gland papillary carcinoma,
+BMGC_DS08624,BMG_DS033942,,,,,,,DOID:7207,lung combined large cell neuroendocrine carcinoma,C1333122,,,MONDO:0004142,lung combined large cell neuroendocrine carcinoma,
+BMGC_DS08625,BMG_DS033944,,,,,,,DOID:5421,lung combined type small cell carcinoma,C1333125,,,MONDO:0003438,combined small cell lung carcinoma,
+BMGC_DS08626,BMG_DS033945,,,,,,,DOID:1618,breast fibroadenoma,C1333137,,,,,
+BMGC_DS08627,BMG_DS033946,,,,,,,DOID:11200,T cell deficiency,C1333147,,,MONDO:0001222,congenital T-cell immunodeficiency,
+BMGC_DS08628,BMG_DS033947,,,,,,,DOID:5465,conjunctival intraepithelial neoplasm,C1333148,,,MONDO:0003453,conjunctival intraepithelial neoplasm,
+BMGC_DS08629,BMG_DS033948,,,,,,,DOID:3641,conus medullaris neoplasm,C1333153,,,MONDO:0002719,conus medullaris neoplasm,
+BMGC_DS08630,BMG_DS033949,,,,,,,DOID:4512,conventional angiosarcoma,C1333155,,,MONDO:0003025,conventional angiosarcoma,
+BMGC_DS08631,BMG_DS033950,,,,,,,DOID:3517,conventional fibrosarcoma,C1333156,,,MONDO:0002677,conventional fibrosarcoma,
+BMGC_DS08632,BMG_DS033951,,,,,,,DOID:5253,conventional leiomyosarcoma,C1333157,,,MONDO:0003348,conventional leiomyosarcoma,
+BMGC_DS08633,BMG_DS033952,,,,,,,DOID:6197,conventional malignant hemangiopericytoma,C1333158,,,MONDO:0003800,conventional malignant hemangiopericytoma,
+BMGC_DS08634,BMG_DS033953,,,,,,,DOID:6198,corneal intraepithelial neoplasm,C1333159,,,MONDO:0003801,corneal intraepithelial neoplasm,
+BMGC_DS08635,BMG_DS033954,,,,,,,DOID:6294,corpus callosum lipoma,C1333160,,,MONDO:0003845,corpus callosum lipoma,
+BMGC_DS08636,BMG_DS033955,,,,,,,DOID:7326,cranial pseudosarcomatous fasciitis,C1333162,,,MONDO:0004186,cranial nodular fasciitis,
+BMGC_DS08637,BMG_DS033957,,,,,,,DOID:10188,skin lipoma,C1333174,,,,,
+BMGC_DS08638,BMG_DS033958,,,,,,,DOID:5712,cutaneous liposarcoma,C1333175,,,MONDO:0003600,cutaneous liposarcoma,
+BMGC_DS08639,BMG_DS033959,,,,,,,DOID:2286,capillary lymphangioma,C1333176,,,MONDO:0024673,skin lymphangioma,
+BMGC_DS08640,BMG_DS033961,,,,,,,DOID:469,deep angioma,C1333265,,,MONDO:0003096,deep hemangioma,
+BMGC_DS08641,BMG_DS033962,,,,,,,DOID:5128,deep leiomyoma,C1333266,,,MONDO:0003289,deep leiomyoma,
+BMGC_DS08642,BMG_DS033963,,,,,,,DOID:7071,spinal cord dermoid cyst,C1333278,,,MONDO:0004096,spinal cord dermoid cyst,
+BMGC_DS08643,BMG_DS033965,,,,,,,DOID:7103,diaphragma sellae meningioma,C1333283,,,MONDO:0004108,diaphragma sellae meningioma,
+BMGC_DS08644,BMG_DS033966,,,,,,,DOID:4855,diencephalic astrocytoma,C1333284,,,MONDO:0003169,diencephalic astrocytomas,
+BMGC_DS08645,BMG_DS033967,,,,,,,DOID:3843,diencephalic neoplasm,C1333286,,,,,
+BMGC_DS08646,BMG_DS033969,449784008,Diffuse infiltrative lymphocytosis syndrome,,,,,DOID:6677,diffuse infiltrative lymphocytosis syndrome,C1333292,,,MONDO:0003963,diffuse infiltrative lymphocytosis syndrome,Diffuse infiltrative lymphocytosis syndrome (disorder) | Diffuse infiltrative lymphocytosis syndrome | DILS - diffuse infiltrative lymphocytosis syndrome
+BMGC_DS08647,BMG_DS033973,,,,,,,DOID:3923,diffuse lipomatosis,C1333298,,,MONDO:0006539,diffuse lipomatosis,
+BMGC_DS08648,BMG_DS033974,,,,,,,DOID:6988,peripheral epithelioid sarcoma,C1333306,,,MONDO:0004060,peripheral epithelioid sarcoma,
+BMGC_DS08649,BMG_DS033975,,,,,,,DOID:5923,distal biliary tract carcinoma,C1333308,,,MONDO:0003707,distal biliary tract carcinoma,
+BMGC_DS08650,BMG_DS033976,,,,,,,DOID:7479,duodenal somatostatinoma,C1333320,,,MONDO:0004236,duodenal somatostatinoma,
+BMGC_DS08651,BMG_DS033977,,,,,,,DOID:7959,duodenal gastrinoma,C1333321,,,MONDO:0004411,duodenal gastrin-producing neuroendocrine tumor,
+BMGC_DS08652,BMG_DS033980,,,,,,,DOID:8307,early invasive cervical adenocarcinoma,C1333369,,,MONDO:0004530,early invasive cervical adenocarcinoma,
+BMGC_DS08653,BMG_DS033981,,,,,,,DOID:8409,microinvasive cervical squamous cell carcinoma,C1333370,,,MONDO:0004552,microinvasive cervical squamous cell carcinoma,
+BMGC_DS08654,BMG_DS033982,,,,,,,DOID:173,eccrine sweat gland neoplasm,C1333371,,,MONDO:0002090,eccrine sweat gland neoplasm,
+BMGC_DS08655,BMG_DS033984,,Ectopic thymus,,,,,DOID:6307,ectopic thymus,C1333375,,MTHU019219,MONDO:0003848,ectopic thymus,
+BMGC_DS08656,BMG_DS033985,,,,,,,DOID:7232,central nervous system embryonal carcinoma,C1333377,,,MONDO:0018843,embryonal carcinoma of the central nervous system,
+BMGC_DS08657,BMG_DS033986,,,,,,,DOID:3278,encapsulated thymoma,C1333383,,,MONDO:0002587,encapsulated thymoma,
+BMGC_DS08658,BMG_DS033987,,,,,,,DOID:6608,endobronchial leiomyoma,C1333386,,,MONDO:0003944,endobronchial leiomyoma,
+BMGC_DS08659,BMG_DS033988,,,,,,,DOID:5533,endometrial squamous cell carcinoma,C1333396,,,MONDO:0006198,endometrial squamous cell carcinoma,
+BMGC_DS08660,BMG_DS033989,,,,,,,DOID:6606,eosinophilic variant of chromophobe renal cell carcinoma,C1333405,,,MONDO:0003942,eosinophilic variant of chromophobe renal cell carcinoma,
+BMGC_DS08661,BMG_DS033990,,,,,,,DOID:5074,high grade ependymoma,C1333407,,,MONDO:0003266,ependymal tumor,
+BMGC_DS08662,BMG_DS033991,,,,,,,DOID:6284,epicardium lipoma,C1333411,,,MONDO:0003840,epicardium lipoma,
+BMGC_DS08663,BMG_DS033992,,,,,,,DOID:4323,epidermolytic acanthoma,C1333414,,,MONDO:0002962,epidermolytic acanthoma,
+BMGC_DS08664,BMG_DS033994,,,,,,,DOID:3617,epidural spinal canal angiolipoma,C1333416,,,MONDO:0002712,epidural spinal canal angiolipoma,
+BMGC_DS08665,BMG_DS033995,,,,,,,DOID:3809,epidural spinal canal meningioma,C1333417,,,MONDO:0002778,epidural spinal canal meningioma,
+BMGC_DS08666,BMG_DS033996,,,,,,,DOID:916,liver benign neoplasm,C1333419,,,,,
+BMGC_DS08667,BMG_DS033997,,,,,,,DOID:4768,epithelial predominant pulmonary blastoma,C1333420,,,MONDO:0003129,epithelial predominant pulmonary blastoma,
+BMGC_DS08668,BMG_DS033998,,,,,,,DOID:7040,uveal epithelioid cell melanoma,C1333422,,,MONDO:0006200,epithelioid cell uveal melanoma,
+BMGC_DS08669,BMG_DS034000,,,,,,,DOID:4878,esophageal adenoid cystic carcinoma,C1333441,,,MONDO:0003186,esophageal adenoid cystic carcinoma,
+BMGC_DS08670,BMG_DS034001,,,,,,,DOID:7051,esophageal basaloid squamous cell carcinoma,C1333443,,,MONDO:0004093,esophageal basaloid carcinoma,
+BMGC_DS08671,BMG_DS034002,,,,,,,DOID:5040,malignant granular cell esophageal tumor,C1333448,,,MONDO:0003251,esophageal granular cell tumor,
+BMGC_DS08672,BMG_DS034003,,,,,,,DOID:8632,Kaposi's sarcoma,C1333453,,,,,
+BMGC_DS08673,BMG_DS034004,,,,,,,DOID:5276,esophagus leiomyosarcoma,C1333454,,,MONDO:0003365,esophagus leiomyosarcoma,
+BMGC_DS08674,BMG_DS034006,,,,,,,DOID:5694,esophagus liposarcoma,C1333456,,,MONDO:0003586,esophagus liposarcoma,
+BMGC_DS08675,BMG_DS034007,,,,,,,DOID:1106,esophagus lymphoma,C1333459,,,MONDO:0001188,esophagus lymphoma,
+BMGC_DS08676,BMG_DS034008,,,,,,,DOID:1108,esophagus melanoma,C1333460,,,MONDO:0001192,esophageal melanoma,
+BMGC_DS08677,BMG_DS034009,,,,,,,DOID:4686,mucoepidermoid esophageal carcinoma,C1333461,,,MONDO:0003093,mucoepidermoid esophageal carcinoma,
+BMGC_DS08678,BMG_DS034010,,,,,,,DOID:5784,esophageal neuroendocrine tumor,C1333462,,,,,
+BMGC_DS08679,BMG_DS034011,,,,,,,DOID:961,neurofibroma of the esophagus,C1333463,,,MONDO:0004837,neurofibroma of the esophagus,
+BMGC_DS08680,BMG_DS034012,,,,,,,DOID:1114,esophagus sarcoma,C1333466,,,MONDO:0001204,esophagus sarcoma,
+BMGC_DS08681,BMG_DS034014,,,,,,,DOID:3747,esophagus verrucous carcinoma,C1333470,,,MONDO:0002762,esophagus verrucous carcinoma,
+BMGC_DS08682,BMG_DS034015,,,,,,,DOID:2766,ethmoid sinus adenocarcinoma,C1333472,,,MONDO:0002418,ethmoid sinus adenocarcinoma,
+BMGC_DS08683,BMG_DS034016,,,,,,,DOID:2764,ethmoid sinus adenoid cystic carcinoma,C1333473,,,MONDO:0006201,ethmoid sinus adenoid cystic carcinoma,
+BMGC_DS08684,BMG_DS034017,,,,,,,DOID:6562,ethmoid sinus inverted papilloma,C1333474,,,MONDO:0003925,ethmoid sinus inverted papilloma,
+BMGC_DS08685,BMG_DS034018,,,,,,,DOID:6854,ethmoid sinus ectopic meningioma,C1333475,,,MONDO:0004014,ethmoid sinus ectopic meningioma,
+BMGC_DS08686,BMG_DS034019,,,,,,,DOID:6559,ethmoid sinus Schneiderian papilloma,C1333476,,,MONDO:0003923,ethmoid sinus Schneiderian papilloma,
+BMGC_DS08687,BMG_DS034020,,,,,,,DOID:2763,ethmoid sinus squamous cell carcinoma,C1333477,,,MONDO:0002416,ethmoid sinus squamous cell carcinoma,
+BMGC_DS08688,BMG_DS034021,,,,,,,DOID:3368,Ewing sarcoma of bone,C1333481,,,MONDO:0021123,Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone,
+BMGC_DS08689,BMG_DS034023,,,,,,,DOID:4287,external ear basal cell carcinoma,C1333491,,,MONDO:0002943,external ear basal cell carcinoma,
+BMGC_DS08690,BMG_DS034024,,,,,,,DOID:4288,external ear carcinoma,C1333492,,,MONDO:0002944,external ear carcinoma,
+BMGC_DS08691,BMG_DS034025,,,,,,,DOID:5538,external ear squamous cell carcinoma,C1333494,,,MONDO:0003501,external ear squamous cell carcinoma,
+BMGC_DS08692,BMG_DS034026,,,,,,,DOID:371,extracranial neuroblastoma,C1333499,,,MONDO:0002749,extracranial neuroblastoma,
+BMGC_DS08693,BMG_DS034027,,,,,,,DOID:5838,extragonadal seminoma,C1333502,,,MONDO:0003668,extragonadal seminoma,
+BMGC_DS08694,BMG_DS034028,,,,,,,DOID:8105,extrahepatic bile duct cystadenoma,C1333504,,,MONDO:0004462,extrahepatic bile duct cystadenoma,
+BMGC_DS08695,BMG_DS034029,,,,,,,DOID:3253,embryonal extrahepatic bile duct rhabdomyosarcoma,C1333505,,,MONDO:0002576,embryonal extrahepatic bile duct rhabdomyosarcoma,
+BMGC_DS08696,BMG_DS034031,,,,,,,DOID:5293,extrahepatic bile duct leiomyosarcoma,C1333508,,,MONDO:0003377,extrahepatic bile duct leiomyosarcoma,
+BMGC_DS08697,BMG_DS034032,,,,,,,DOID:10209,extrahepatic bile duct lipoma,C1333509,,,MONDO:0000978,extrahepatic bile duct lipoma,
+BMGC_DS08698,BMG_DS034033,,,,,,,DOID:7503,extrahepatic bile duct papillary adenoma,C1333510,,,MONDO:0004250,extrahepatic bile duct papillary adenoma,
+BMGC_DS08699,BMG_DS034034,,,,,,,DOID:7752,extrahepatic biliary papillomatosis,C1333511,,,MONDO:0004353,extrahepatic biliary papillomatosis,
+BMGC_DS08700,BMG_DS034035,,,,,,,DOID:4232,extraosseous Ewing sarcoma,C1333514,,,MONDO:0021039,extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor,
+BMGC_DS08701,BMG_DS034036,,,,,,,DOID:3706,fallopian tube adenocarcinoma,C1333590,,,MONDO:0002746,fallopian tube adenocarcinoma,
+BMGC_DS08702,BMG_DS034037,,,,,,,DOID:5301,fallopian tube clear cell adenocarcinoma,C1333591,,,MONDO:0003383,fallopian tube clear cell adenocarcinoma,
+BMGC_DS08703,BMG_DS034038,,,,,,,DOID:5831,fallopian tube endometrioid adenocarcinoma,C1333592,,,MONDO:0003666,fallopian tube endometrioid adenocarcinoma,
+BMGC_DS08704,BMG_DS034039,,,,,,,DOID:8186,fallopian tube gestational choriocarcinoma,C1333593,,,MONDO:0004489,fallopian tube gestational choriocarcinoma,
+BMGC_DS08705,BMG_DS034040,,,,,,,DOID:5597,fallopian tube papillary adenocarcinoma,C1333595,,,MONDO:0003535,fallopian tube papillary adenocarcinoma,
+BMGC_DS08706,BMG_DS034041,,,,,,,DOID:5540,fallopian tube squamous cell carcinoma,C1333596,,,MONDO:0003503,fallopian tube squamous cell carcinoma,
+BMGC_DS08707,BMG_DS034042,,,,,,,DOID:7986,cerebral falx meningioma,C1333597,,,MONDO:0004422,cerebral falx meningioma,
+BMGC_DS08708,BMG_DS034044,,,,,,,DOID:5484,fibrous synovial sarcoma,C1333616,,,MONDO:0003465,fibrous synovial sarcoma,
+BMGC_DS08709,BMG_DS034045,,,,,,,DOID:6841,flat ductal epithelial atypia,C1333620,,,MONDO:0004008,flat ductal epithelial atypia,
+BMGC_DS08710,BMG_DS034049,,,,,,,DOID:4708,foramen magnum meningioma,C1333630,,,MONDO:0003109,foramen magnum meningioma,
+BMGC_DS08711,BMG_DS034050,,,,,,,DOID:8000,frontal convexity meningioma,C1333643,,,MONDO:0004426,frontal convexity meningioma,
+BMGC_DS08712,BMG_DS034051,,,,,,,DOID:8060,frontal sinus inverted papilloma,C1333644,,,MONDO:0004448,frontal sinus inverted papilloma,
+BMGC_DS08713,BMG_DS034052,,,,,,,DOID:6054,frontal sinus Schneiderian papilloma,C1333645,,,MONDO:0003752,frontal sinus Schneiderian papilloma,
+BMGC_DS08714,BMG_DS034053,,,,,,,DOID:2441,frontal sinus squamous cell carcinoma,C1333646,,,MONDO:0002301,frontal sinus squamous cell carcinoma,
+BMGC_DS08715,BMG_DS034054,,,,,,,DOID:5627,adenosquamous gallbladder carcinoma,C1333741,,,MONDO:0006217,gallbladder adenosquamous carcinoma,
+BMGC_DS08716,BMG_DS034055,,,,,,,DOID:4513,gallbladder angiosarcoma,C1333742,,,MONDO:0003026,gallbladder angiosarcoma,
+BMGC_DS08717,BMG_DS034056,,,,,,,DOID:8632,Kaposi's sarcoma,C1333744,,,,,
+BMGC_DS08718,BMG_DS034058,,,,,,,DOID:5275,gallbladder leiomyosarcoma,C1333746,,,MONDO:0003364,gallbladder leiomyosarcoma,
+BMGC_DS08719,BMG_DS034060,,,,,,,DOID:8135,gallbladder lymphoma,C1333748,,,MONDO:0004474,gallbladder lymphoma,
+BMGC_DS08720,BMG_DS034061,,,,,,,DOID:8167,gallbladder melanoma,C1333749,,,MONDO:0004484,gallbladder melanoma,
+BMGC_DS08721,BMG_DS034062,,,,,,,DOID:6998,gallbladder mucinous carcinoma,C1333750,,,MONDO:0004067,gallbladder mucinous adenocarcinoma,
+BMGC_DS08722,BMG_DS034063,,,,,,,DOID:5150,neurofibroma of gallbladder,C1333751,,,MONDO:0003303,neurofibroma of gallbladder,
+BMGC_DS08723,BMG_DS034066,,,,,,,DOID:4057,gallbladder rhabdomyosarcoma,C1333756,,,MONDO:0002856,gallbladder rhabdomyosarcoma,
+BMGC_DS08724,BMG_DS034067,,,,,,,DOID:4058,gallbladder sarcoma,C1333757,,,MONDO:0002857,gallbladder sarcoma,
+BMGC_DS08725,BMG_DS034068,,,,,,,DOID:3499,gallbladder signet ring cell adenocarcinoma,C1333758,,,MONDO:0002667,gallbladder signet ring cell adenocarcinoma,
+BMGC_DS08726,BMG_DS034069,,,,,,,DOID:7133,gallbladder small cell carcinoma,C1333759,,,MONDO:0006219,gallbladder small cell neuroendocrine carcinoma,
+BMGC_DS08727,BMG_DS034070,,,,,,,DOID:7635,Gasserian ganglion meningioma,C1333760,,,MONDO:0004313,gasserian ganglion meningioma,
+BMGC_DS08728,BMG_DS034071,,,,,,,DOID:5635,gastric adenosquamous carcinoma,C1333761,,,MONDO:0006034,gastric adenosquamous carcinoma,
+BMGC_DS08729,BMG_DS034072,,,,,,,DOID:6271,gastric cardia adenocarcinoma,C1333762,,,MONDO:0003835,gastric cardia adenocarcinoma,
+BMGC_DS08730,BMG_DS034073,,,,,,,DOID:6270,gastric cardia carcinoma,C1333763,,,MONDO:0003834,gastric cardia carcinoma,
+BMGC_DS08731,BMG_DS034074,,,,,,,DOID:6225,Cronkhite-Canada syndrome,C1333764,,,,,
+BMGC_DS08732,BMG_DS034075,,,,,,,DOID:5579,gastric gastrinoma,C1333767,,,MONDO:0003524,gastric gastrin-producing neuroendocrine tumor,
+BMGC_DS08733,BMG_DS034076,,,,,,,DOID:4716,malignant gastric germ cell tumor,C1333769,,,,,
+BMGC_DS08734,BMG_DS034078,,,,,,,DOID:8632,Kaposi's sarcoma,C1333776,,,,,
+BMGC_DS08735,BMG_DS034080,,,,,,,DOID:5700,gastric liposarcoma,C1333778,,,MONDO:0003592,gastric liposarcoma,
+BMGC_DS08736,BMG_DS034083,,,,,,,DOID:4715,gastric neuroendocrine neoplasm,C1333783,,,MONDO:0003111,gastric neuroendocrine neoplasm,
+BMGC_DS08737,BMG_DS034085,,,,,,,DOID:5593,gastric papillary adenocarcinoma,C1333785,,,MONDO:0006228,gastric papillary adenocarcinoma,
+BMGC_DS08738,BMG_DS034086,,,,,,,DOID:6703,gastric pylorus carcinoma,C1333787,,,MONDO:0003971,gastric pylorus carcinoma,
+BMGC_DS08739,BMG_DS034087,,,,,,,DOID:6552,gastric small cell carcinoma,C1333788,,,MONDO:0006229,gastric small cell neuroendocrine carcinoma,
+BMGC_DS08740,BMG_DS034088,,,,,,,DOID:5516,gastric squamous cell carcinoma,C1333789,,,MONDO:0006230,gastric squamous cell carcinoma,
+BMGC_DS08741,BMG_DS034089,,,,,,,DOID:5561,gastric teratoma,C1333790,,,MONDO:0003513,gastric teratoma,
+BMGC_DS08742,BMG_DS034090,,,,,,,DOID:6595,gastric tubular adenocarcinoma,C1333791,,,MONDO:0006035,gastric tubular adenocarcinoma,
+BMGC_DS08743,BMG_DS034092,,,,,,,DOID:4148,gastrointestinal neuroendocrine benign tumor,C1333799,,,MONDO:0024503,digestive system neuroendocrine neoplasm,
+BMGC_DS08744,BMG_DS034093,,,,,,,DOID:4438,central nervous system germinoma,C1333813,,,MONDO:0002999,central nervous system germinoma,
+BMGC_DS08745,BMG_DS034094,,,,,,,DOID:5774,giant hemangioma,C1333817,,,MONDO:0003643,giant hemangioma,
+BMGC_DS08746,BMG_DS034095,,,,,,,DOID:8420,malignant glandular tumor of peripheral nerve sheath,C1333821,,,MONDO:0004559,malignant glandular tumor of peripheral nerve sheath,
+BMGC_DS08747,BMG_DS034096,,,,,,,DOID:6906,glomangiomatosis,C1333824,,,MONDO:0004035,glomangiomatosis,
+BMGC_DS08748,BMG_DS034097,,,,,,,DOID:5258,granular cell leiomyosarcoma,C1333871,,,MONDO:0003350,granular cell leiomyosarcoma,
+BMGC_DS08749,BMG_DS034098,,,,,,,DOID:5047,granular cell tumor of the sellar region,C1333873,,,MONDO:0003256,neurohypophysis granular cell tumor,
+BMGC_DS08750,BMG_DS034099,,,,,,,DOID:4561,granulomatous endometritis,C1333876,,,MONDO:0003052,granulomatous endometritis,
+BMGC_DS08751,BMG_DS034100,,,,,,,DOID:5822,gray zone lymphoma,C1333878,,,MONDO:0003658,"B-cell lymphoma, unclassifiable, with features intermediate between diffuse large b-cell lymphoma and classical Hodgkin lymphoma",
+BMGC_DS08752,BMG_DS034105,,,,,,,DOID:3317,hepatic angiomyolipoma,C1333962,,,MONDO:0002605,hepatic angiomyolipoma,
+BMGC_DS08753,BMG_DS034106,,,,,,,DOID:907,liver fibroma,C1333965,,,MONDO:0004705,liver solitary fibrous tumor,
+BMGC_DS08754,BMG_DS034107,,,,,,,DOID:8022,liver fibrosarcoma,C1333966,,,MONDO:0004435,liver fibrosarcoma,
+BMGC_DS08755,BMG_DS034108,,,,,,,DOID:918,liver inflammatory pseudotumor,C1333967,,,MONDO:0004726,liver inflammatory myofibroblastic tumor,
+BMGC_DS08756,BMG_DS034109,,,,,,,DOID:917,liver leiomyoma,C1333968,,,MONDO:0004723,liver leiomyoma,
+BMGC_DS08757,BMG_DS034110,,,,,,,DOID:5296,liver leiomyosarcoma,C1333969,,,MONDO:0003378,liver leiomyosarcoma,
+BMGC_DS08758,BMG_DS034111,,,,,,,DOID:10190,liver lipoma,C1333970,,,MONDO:0000965,liver lipoma,
+BMGC_DS08759,BMG_DS034113,,,,,,,DOID:6370,hepatic osteogenic sarcoma,C1333974,,,MONDO:0003866,liver extraskeletal osteosarcoma,
+BMGC_DS08760,BMG_DS034114,,,,,,,DOID:4047,liver rhabdomyosarcoma,C1333975,,,MONDO:0002849,liver rhabdomyosarcoma,
+BMGC_DS08761,BMG_DS034115,,,,,,,DOID:916,liver benign neoplasm,C1333976,,,MONDO:0024477,liver and intrahepatic bile duct neoplasm,
+BMGC_DS08762,BMG_DS034116,,,,,,,,,C1333984,,,MONDO:0019474,hepatosplenic T-cell lymphoma,
+BMGC_DS08763,BMG_DS034117,,,,,,,DOID:7192,hereditary conventional renal cell carcinoma,C1333985,,,MONDO:0018492,hereditary clear cell renal cell carcinoma,
+BMGC_DS08764,BMG_DS034118,,,,,,,DOID:7996,familial glomangioma,C1333987,,,,,
+BMGC_DS08765,BMG_DS034119,,,,,,,DOID:4586,familial meningioma,C1333989,,,,,
+BMGC_DS08766,BMG_DS034120,,,,,,,,,C1333990,,,MONDO:0018630,hereditary nonpolyposis colon cancer,
+BMGC_DS08767,BMG_DS034121,,,,,,,,,C1333991,,609310,MONDO:0012249,Lynch syndrome 2,
+BMGC_DS08768,BMG_DS034122,,,,,,,DOID:6901,familiar ovarian carcinoma,C1333992,,,MONDO:0100514,familial ovarian carcinoma,
+BMGC_DS08769,BMG_DS034123,,,,,,,DOID:6102,herpetic gastritis,C1333996,,,MONDO:0003769,herpetic gastritis,
+BMGC_DS08770,BMG_DS034126,,,,,,,DOID:5621,histiocytic and dendritic cell cancer,C1334030,,,MONDO:0006247,histiocytic and dendritic cell neoplasm,
+BMGC_DS08771,BMG_DS034129,,,,,,,DOID:13407,hypercalcemic sarcoidosis,C1334067,,,MONDO:0001709,hypercalcemic sarcoidosis,
+BMGC_DS08772,BMG_DS034130,,,,,,,DOID:2959,hyperimmunoglobulin syndrome,C1334069,,,MONDO:0002468,hyperimmunoglobulin syndrome,
+BMGC_DS08773,BMG_DS034132,,,,,,,DOID:3428,granulomatous myositis,C1334150,,,MONDO:0002644,idiopathic granulomatous myositis,
+BMGC_DS08774,BMG_DS034133,,,,,,,DOID:6948,malignant gastric teratoma,C1334151,,,MONDO:0004048,immature gastric teratoma,
+BMGC_DS08775,BMG_DS034136,,,,,,,DOID:5251,inflammatory leiomyosarcoma,C1334179,,,MONDO:0003347,inflammatory leiomyosarcoma,
+BMGC_DS08776,BMG_DS034137,,,,,,,DOID:6192,malignant inflammatory fibrous histiocytoma,C1334180,,,MONDO:0006480,"undifferentiated pleomorphic sarcoma, inflammatory variant",
+BMGC_DS08777,BMG_DS034138,,,,,,,DOID:6996,intermediate cell type choroid melanoma,C1334208,,,MONDO:0004065,intermediate cell type choroid melanoma,
+BMGC_DS08778,BMG_DS034139,,,,,,,DOID:6997,intermediate cell type ciliary body melanoma,C1334209,,,MONDO:0004066,intermediate cell type ciliary body melanoma,
+BMGC_DS08779,BMG_DS034140,,,,,,,DOID:6993,iris mixed cell melanoma,C1334210,,,MONDO:0004063,intermediate cell type iris melanoma,
+BMGC_DS08780,BMG_DS034142,,,,,,,DOID:5990,internal auditory canal meningioma,C1334227,,,MONDO:0003722,internal auditory canal meningioma,
+BMGC_DS08781,BMG_DS034143,,,,,,,DOID:4119,intestinal neuroendocrine benign tumor,C1334231,,,MONDO:0002883,intestinal neuroendocrine neoplasm,
+BMGC_DS08782,BMG_DS034144,,,,,,,DOID:6113,intracerebral cystic meningioma,C1334236,,,MONDO:0003773,intracerebral cystic meningioma,
+BMGC_DS08783,BMG_DS034145,,,,,,,DOID:2516,intracranial cavernous angioma,C1334237,,,MONDO:0002327,intracranial cavernous angioma,
+BMGC_DS08784,BMG_DS034146,,,,,,,DOID:7903,intracranial chondrosarcoma,C1334238,,,MONDO:0004392,intracranial extraskeletal myxoid chondrosarcoma,
+BMGC_DS08785,BMG_DS034147,,,,,,,DOID:5714,intracranial liposarcoma,C1334242,,,MONDO:0003602,intracranial liposarcoma,
+BMGC_DS08786,BMG_DS034151,,,,,,,DOID:1628,intraductal papillary breast neoplasm,C1334252,,,MONDO:0002061,intraductal papillary breast neoplasm,
+BMGC_DS08787,BMG_DS034152,,,,,,,DOID:4846,cauda equina intradural extramedullary astrocytoma,C1334254,,,MONDO:0003163,cauda equina intradural extramedullary astrocytoma,
+BMGC_DS08788,BMG_DS034153,,,,,,,DOID:5615,spinal canal intradural extramedullary neoplasm,C1334255,,,MONDO:0003545,intradural extramedullary spinal canal neoplasm,
+BMGC_DS08789,BMG_DS034154,,,,,,,DOID:6733,intrahepatic bile duct cystadenoma,C1334257,,,MONDO:0003979,intrahepatic bile duct cystadenoma,
+BMGC_DS08790,BMG_DS034155,,,,,,,DOID:8230,intrahepatic biliary papillomatosis,C1334258,,,MONDO:0004509,intrahepatic biliary papillomatosis,
+BMGC_DS08791,BMG_DS034156,,,,,,,DOID:3639,spinal cord intramedullary teratoma,C1334259,,,MONDO:0002717,spinal cord intramedullary teratoma,
+BMGC_DS08792,BMG_DS034157,,,,,,,DOID:4141,intraorbital meningioma,C1334261,,,MONDO:0002888,intraorbital meningioma,
+BMGC_DS08793,BMG_DS034158,,,,,,,DOID:1140,spinal canal and spinal cord meningioma,C1334264,,,MONDO:0001279,intraspinal meningioma,
+BMGC_DS08794,BMG_DS034159,,,,,,,DOID:4266,intravascular angioleiomyoma,C1334267,,,MONDO:0002934,intravascular angioleiomyoma,
+BMGC_DS08795,BMG_DS034160,,,,,,,DOID:3772,intraventricular meningioma,C1334271,,,MONDO:0002772,intraventricular meningioma,
+BMGC_DS08796,BMG_DS034163,,,,,,,DOID:6477,invasive bladder transitional cell carcinoma,C1334281,,,MONDO:0003890,infiltrating bladder urothelial carcinoma,
+BMGC_DS08797,BMG_DS034164,,,,,,,DOID:5433,urinary tract papillary transitional cell benign neoplasm,C1334282,,,MONDO:0021109,inverted urothelial papilloma,
+BMGC_DS08798,BMG_DS034165,,,,,,,DOID:7328,iris spindle cell melanoma,C1334287,,,MONDO:0004188,iris spindle cell melanoma,
+BMGC_DS08799,BMG_DS034167,,,,,,,DOID:3216,jejunal somatostatinoma,C1334297,,,MONDO:0002563,jejunal somatostatinoma,
+BMGC_DS08800,BMG_DS034168,,,,,,,DOID:6110,jugular foramen meningioma,C1334298,,,MONDO:0003771,jugular foramen meningioma,
+BMGC_DS08801,BMG_DS034169,,,,,,,DOID:6735,schwannoma of jugular foramen,C1334300,,,MONDO:0003980,schwannoma of jugular foramen,
+BMGC_DS08802,BMG_DS034171,,,,,,,DOID:8632,Kaposi's sarcoma,C1334318,,,,,
+BMGC_DS08803,BMG_DS034172,,,,,,,DOID:3116,kidney benign neoplasm,C1334323,,,,,
+BMGC_DS08804,BMG_DS034173,,,,,,,DOID:13389,labia majora carcinoma,C1334356,,,MONDO:0001702,labia majora carcinoma,
+BMGC_DS08805,BMG_DS034174,,,,,,,DOID:1293,labia minora carcinoma,C1334357,,,MONDO:0001602,labia minora carcinoma,
+BMGC_DS08806,BMG_DS034175,,,,,,,DOID:293,lacrimal gland carcinoma,C1334358,,,MONDO:0002463,lacrimal gland carcinoma,
+BMGC_DS08807,BMG_DS034176,,,,,,,DOID:4685,lacrimal gland mucoepidermoid carcinoma,C1334359,,,MONDO:0003092,lacrimal gland mucoepidermoid carcinoma,
+BMGC_DS08808,BMG_DS034178,,,,,,,DOID:292,lacrimal system cancer,C1334361,,,MONDO:0002460,lacrimal system cancer,
+BMGC_DS08809,BMG_DS034179,,,,,,,DOID:4321,large cell acanthoma,C1334362,,,MONDO:0002961,large cell acanthoma,
+BMGC_DS08810,BMG_DS034180,,,,,,,DOID:6658,pulmonary large cell neuroendocrine carcinoma,C1334363,,,MONDO:0003960,pulmonary large cell neuroendocrine carcinoma,
+BMGC_DS08811,BMG_DS034181,,,,,,,DOID:4553,thymus large cell carcinoma,C1334364,,,MONDO:0003047,thymic large cell neuroendocrine carcinoma,
+BMGC_DS08812,BMG_DS034182,,,,,,,DOID:4869,laryngeal adenoid cystic carcinoma,C1334368,,,MONDO:0006264,laryngeal adenoid cystic carcinoma,
+BMGC_DS08813,BMG_DS034183,,,,,,,DOID:10070,larynx leiomyoma,C1334370,,,MONDO:0000934,laryngeal leiomyoma,
+BMGC_DS08814,BMG_DS034184,,,,,,,DOID:5288,larynx leiomyosarcoma,C1334371,,,MONDO:0003374,laryngeal leiomyosarcoma,
+BMGC_DS08815,BMG_DS034185,,,,,,,DOID:5696,larynx liposarcoma,C1334372,,,MONDO:0003588,larynx liposarcoma,
+BMGC_DS08816,BMG_DS034186,,,,,,,DOID:4688,laryngeal mucoepidermoid carcinoma,C1334373,,,MONDO:0003095,laryngeal mucoepidermoid carcinoma,
+BMGC_DS08817,BMG_DS034187,,,,,,,DOID:5457,laryngeal neuroendocrine tumor,C1334374,,,MONDO:0015070,laryngeal neuroendocrine neoplasm,
+BMGC_DS08818,BMG_DS034188,,,,,,,DOID:2877,larynx sarcoma,C1334377,,,MONDO:0002448,laryngeal sarcoma,
+BMGC_DS08819,BMG_DS034189,,,,,,,DOID:7144,laryngeal small cell carcinoma,C1334378,,,MONDO:0006265,laryngeal small cell carcinoma,
+BMGC_DS08820,BMG_DS034190,,,,,,,DOID:6115,lateral ventricle meningioma,C1334380,,,MONDO:0003775,lateral ventricle meningioma,
+BMGC_DS08821,BMG_DS034193,,,,,,,DOID:6085,meningeal melanoma,C1334386,,,MONDO:0003761,leptomeningeal melanoma,
+BMGC_DS08822,BMG_DS034194,,,,,,,DOID:3368,Ewing sarcoma of bone,C1334406,,,,,
+BMGC_DS08823,BMG_DS034195,,,,,,,DOID:3369,Ewing sarcoma,C1334408,,,,,
+BMGC_DS08824,BMG_DS034196,,,,,,,DOID:0050902,medulloblastoma,C1334410,,,,,
+BMGC_DS08825,BMG_DS034198,,,,,,,DOID:8239,lower clivus meningioma,C1334434,,,MONDO:0004511,lower clivus meningioma,
+BMGC_DS08826,BMG_DS034199,,,,,,,DOID:7515,lumbar spinal canal and spinal cord meningioma,C1334436,,,MONDO:0004256,lumbar spinal canal and spinal cord meningioma,
+BMGC_DS08827,BMG_DS034200,,,,,,,DOID:8389,lumbar plexus neoplasm,C1334437,,,MONDO:0004546,lumbar plexus neoplasm,
+BMGC_DS08828,BMG_DS034202,,,,,,,DOID:4872,lung adenoid cystic carcinoma,C1334439,,,MONDO:0003181,lung adenoid cystic carcinoma,
+BMGC_DS08829,BMG_DS034204,,,,,,,DOID:8207,hilar lung carcinoma,C1334445,,,MONDO:0004499,lung hilum carcinoma,
+BMGC_DS08830,BMG_DS034205,,,,,,,DOID:5136,lung leiomyoma,C1334447,,,MONDO:0003293,lung leiomyoma,
+BMGC_DS08831,BMG_DS034206,,,,,,,DOID:5265,lung leiomyosarcoma,C1334448,,,MONDO:0003357,lung leiomyosarcoma,
+BMGC_DS08832,BMG_DS034207,,,,,,,DOID:5764,lung meningioma,C1334450,,,MONDO:0003638,lung meningioma,
+BMGC_DS08833,BMG_DS034208,,,,,,,DOID:5410,pulmonary neuroendocrine tumor,C1334452,,,MONDO:0005454,lung neuroendocrine neoplasm,
+BMGC_DS08834,BMG_DS034210,,,,,,,DOID:5766,pulmonary sclerosing hemangioma,C1334455,,,,,
+BMGC_DS08835,BMG_DS034211,,,,,,,DOID:8632,Kaposi's sarcoma,C1334457,,,,,
+BMGC_DS08836,BMG_DS034212,,,,,,,DOID:7381,lymphohistiocytoid mesothelioma,C1334464,,,MONDO:0004205,lymphohistiocytoid mesothelioma,
+BMGC_DS08837,BMG_DS034213,,,,,,,DOID:5798,macrotrabecular hepatoblastoma,C1334543,,,MONDO:0003651,macrotrabecular hepatoblastoma,
+BMGC_DS08838,BMG_DS034218,,,,,,,DOID:6276,malignant ACTH producing neoplasm of pituitary gland,C1334556,,,MONDO:0006069,ACTH-producing pituitary gland carcinoma,
+BMGC_DS08839,BMG_DS034219,,,,,,,DOID:1319,brain cancer,C1334557,,,,,
+BMGC_DS08840,BMG_DS034220,,,,,,,DOID:6333,adult intracranial malignant hemangiopericytoma,C1334558,,,MONDO:0003857,adult intracranial malignant hemangiopericytoma,
+BMGC_DS08841,BMG_DS034221,,,,,,,DOID:8352,aortic malignant tumor,C1334560,,,MONDO:0004539,aortic malignant tumor,
+BMGC_DS08842,BMG_DS034222,,,,,,,DOID:4934,apocrine sweat gland cancer,C1334561,,,MONDO:0003215,apocrine sweat gland cancer,
+BMGC_DS08843,BMG_DS034223,,,,,,,DOID:1642,breast adenomyoepithelioma,C1334564,,,,,
+BMGC_DS08844,BMG_DS034224,,,,,,,DOID:7983,breast malignant eccrine spiradenoma,C1334565,,,MONDO:0004420,breast malignant eccrine spiradenoma,
+BMGC_DS08845,BMG_DS034225,,,,,,,DOID:14535,malignant cardiac germ cell tumor,C1334566,,,MONDO:0001991,malignant cardiac germ cell tumor,
+BMGC_DS08846,BMG_DS034226,,,,,,,DOID:6034,heart malignant hemangiopericytoma,C1334567,,,MONDO:0003743,heart malignant hemangiopericytoma,
+BMGC_DS08847,BMG_DS034227,,,,,,,DOID:14534,malignant cardiac peripheral nerve sheath neoplasm,C1334569,,,MONDO:0001990,malignant cardiac peripheral nerve sheath neoplasm,
+BMGC_DS08848,BMG_DS034229,,,,,,,DOID:6579,chest wall bone cancer,C1334572,,,MONDO:0003933,chest wall bone cancer,
+BMGC_DS08849,BMG_DS034230,,,,,,,DOID:8149,malignant childhood germ cell neoplasm,C1334574,,,MONDO:0004479,malignant childhood germ cell neoplasm,
+BMGC_DS08850,BMG_DS034231,,,,,,,DOID:7639,malignant granular cell skin tumor,C1334575,,,MONDO:0004314,malignant cutaneous granular cell skin tumor,
+BMGC_DS08851,BMG_DS034232,,,,,,,DOID:3843,diencephalic neoplasm,C1334576,,,MONDO:0002786,diencephalic cancer,
+BMGC_DS08852,BMG_DS034233,,,,,,,DOID:4921,eccrine sweat gland cancer,C1334577,,,MONDO:0005506,eccrine sweat gland cancer,
+BMGC_DS08853,BMG_DS034234,,,,,,,DOID:4717,extragonadal germ cell cancer,C1334581,,,MONDO:0003113,extragonadal germ cell cancer,
+BMGC_DS08854,BMG_DS034235,,,,,,,DOID:5677,malignant extragonadal nonseminomatous germ cell tumor,C1334582,,,MONDO:0003578,extragonadal nonseminomatous germ cell tumor,
+BMGC_DS08855,BMG_DS034237,,,,,,,DOID:10536,malignant gastric granular cell tumor,C1334585,,,MONDO:0001057,malignant gastric granular cell tumor,
+BMGC_DS08856,BMG_DS034238,,,,,,,DOID:6256,malignant growth hormone secreting neoplasm of pituitary,C1334587,,,MONDO:0003828,growth hormone-producing pituitary gland carcinoma,
+BMGC_DS08857,BMG_DS034239,,,,,,,DOID:6086,malignant leptomeningeal neoplasm,C1334596,,,MONDO:0003762,malignant leptomeningeal tumor,
+BMGC_DS08858,BMG_DS034241,,,,,,,DOID:6209,malignant mediastinum hemangiopericytoma,C1334598,,,MONDO:0003809,malignant mediastinum hemangiopericytoma,
+BMGC_DS08859,BMG_DS034243,,,,,,,DOID:7077,malignant melanocytic peripheral nerve sheath tumor of mediastinum,C1334600,,,MONDO:0004098,malignant melanocytic peripheral nerve sheath tumor of mediastinum,
+BMGC_DS08860,BMG_DS034244,,,,,,,DOID:5088,mixed epithelial stromal tumour,C1334602,,,MONDO:0024711,malignant mixed epithelial stromal tumor of the kidney,
+BMGC_DS08861,BMG_DS034245,,,,,,,DOID:4236,carcinosarcoma,C1334603,,,,,
+BMGC_DS08862,BMG_DS034247,,,,,,,DOID:3316,perivascular tumor,C1334611,,,,,
+BMGC_DS08863,BMG_DS034248,,,,,,,DOID:1660,malignant pineal area germ cell neoplasm,C1334612,,,MONDO:0002073,malignant pineal area germ cell neoplasm,
+BMGC_DS08864,BMG_DS034249,,,,,,,DOID:5396,prolactin producing pituitary tumor,C1334614,,,MONDO:0006388,prolactin-producing pituitary gland carcinoma,
+BMGC_DS08865,BMG_DS034250,,,,,,,DOID:10289,prostate malignant phyllodes tumor,C1334615,,,MONDO:0000994,malignant prostate phyllodes tumor,
+BMGC_DS08866,BMG_DS034251,,,,,,,DOID:175,vascular cancer,C1334616,,,,,
+BMGC_DS08867,BMG_DS034252,,,,,,,DOID:175,vascular cancer,C1334617,,,,,
+BMGC_DS08868,BMG_DS034254,,,,,,,DOID:4043,skeletal muscle cancer,C1334619,,,MONDO:0002847,skeletal muscle cancer,
+BMGC_DS08869,BMG_DS034255,,,,,,,DOID:4230,smooth muscle cancer,C1334620,,,MONDO:0002924,smooth muscle cancer,
+BMGC_DS08870,BMG_DS034256,,,,,,,DOID:2706,synovium cancer,C1334624,,,MONDO:0002403,synovium cancer,
+BMGC_DS08871,BMG_DS034257,,,,,,,DOID:5345,testicular non-seminomatous germ cell cancer,C1334625,,,MONDO:0003403,testicular non-seminomatous germ cell cancer,
+BMGC_DS08872,BMG_DS034258,,,,,,,DOID:6274,malignant thyroid stimulating hormone producing neoplasm of pituitary gland,C1334627,,,MONDO:0003836,malignant thyroid stimulating hormone producing neoplasm of pituitary gland,
+BMGC_DS08873,BMG_DS034259,,,,,,,DOID:4114,uterine body mixed cancer,C1334628,,,MONDO:0002879,uterine body mixed cancer,
+BMGC_DS08874,BMG_DS034260,,,,,,,DOID:175,vascular cancer,C1334630,,,,,
+BMGC_DS08875,BMG_DS034261,,,,,,,DOID:6839,breast intraductal proliferative lesion,C1334631,,,MONDO:0004007,breast intraductal proliferative lesion,
+BMGC_DS08876,BMG_DS034262,,,,,,,DOID:706,mature B-cell neoplasm,C1334633,,,MONDO:0004949,neoplasm of mature B-cells,
+BMGC_DS08877,BMG_DS034263,,,,,,,DOID:8118,mature gastric teratoma,C1334635,,,MONDO:0004467,mature gastric teratoma,
+BMGC_DS08878,BMG_DS034264,,,,,,,DOID:6231,mature teratoma of the ovary,C1334637,,,MONDO:0003820,mature ovarian teratoma,
+BMGC_DS08879,BMG_DS034267,,,,,,,DOID:7684,maxillary sinus adenocarcinoma,C1334642,,,MONDO:0004328,maxillary sinus adenocarcinoma,
+BMGC_DS08880,BMG_DS034268,,,,,,,DOID:7198,maxillary sinus adenoid cystic carcinoma,C1334643,,,MONDO:0006297,maxillary sinus adenoid cystic carcinoma,
+BMGC_DS08881,BMG_DS034269,,,,,,,DOID:867,maxillary sinus cholesteatoma,C1334644,,,MONDO:0006577,maxillary sinus cholesteatoma,
+BMGC_DS08882,BMG_DS034270,,,,,,,DOID:7868,maxillary sinus inverted papilloma,C1334645,,,MONDO:0004384,maxillary sinus inverted papilloma,
+BMGC_DS08883,BMG_DS034271,,,,,,,DOID:8093,maxillary sinus Schneiderian papilloma,C1334646,,,MONDO:0004457,maxillary sinus Schneiderian papilloma,
+BMGC_DS08884,BMG_DS034272,,,,,,,DOID:7910,maxillary sinus squamous cell carcinoma,C1334647,,,MONDO:0004394,maxillary sinus squamous cell carcinoma,
+BMGC_DS08885,BMG_DS034273,,,,,,,DOID:4525,mediastinum angiosarcoma,C1334649,,,MONDO:0003034,mediastinum angiosarcoma,
+BMGC_DS08886,BMG_DS034274,,,,,,,DOID:10661,mediastinum ganglioneuroblastoma,C1334653,,,MONDO:0001096,mediastinum ganglioneuroblastoma,
+BMGC_DS08887,BMG_DS034275,,,,,,,,,C1334655,,,MONDO:0021067,mediastinal germ cell tumor,
+BMGC_DS08888,BMG_DS034276,,,,,,,DOID:5046,mediastinal granular cell myoblastoma,C1334656,,,MONDO:0003255,mediastinal granular cell myoblastoma,
+BMGC_DS08889,BMG_DS034277,,,,,,,DOID:6867,mediastinal gray zone lymphoma,C1334657,,,MONDO:0004020,mediastinal gray zone lymphoma,
+BMGC_DS08890,BMG_DS034279,,,,,,,DOID:5292,mediastinum leiomyosarcoma,C1334660,,,MONDO:0003376,mediastinum leiomyosarcoma,
+BMGC_DS08891,BMG_DS034280,,,,,,,DOID:3926,mediastinal lipomatosis,C1334662,,,MONDO:0006578,mediastinal lipomatosis,
+BMGC_DS08892,BMG_DS034281,,,,,,,DOID:5713,mediastinum liposarcoma,C1334663,,,MONDO:0003601,mediastinum liposarcoma,
+BMGC_DS08893,BMG_DS034282,,,,,,,DOID:6868,mediastinal malignant lymphoma,C1334665,,,MONDO:0004021,mediastinal malignant lymphoma,
+BMGC_DS08894,BMG_DS034283,,,,,,,DOID:6484,mediastinal melanocytic neurilemmoma,C1334668,,,MONDO:0003894,mediastinal melanocytic neurilemmoma,
+BMGC_DS08895,BMG_DS034284,,,,,,,DOID:5560,mediastinal mesenchymal tumor,C1334669,,,MONDO:0003512,mediastinal mesenchymal tumor,
+BMGC_DS08896,BMG_DS034285,,,,,,,DOID:4691,malignant mediastinal neurogenic neoplasm,C1334672,,,MONDO:0003098,mediastinal neural neoplasm,
+BMGC_DS08897,BMG_DS034286,,,,,,,DOID:10660,mediastinum neuroblastoma,C1334673,,,MONDO:0001095,mediastinum neuroblastoma,
+BMGC_DS08898,BMG_DS034287,,,,,,,DOID:12064,mediastinum neurofibroma,C1334674,,,MONDO:0001426,mediastinum neurofibroma,
+BMGC_DS08899,BMG_DS034288,,,,,,,DOID:6208,mediastinal osteogenic sarcoma,C1334675,,,MONDO:0003808,mediastinal extraskeletal osteosarcoma,
+BMGC_DS08900,BMG_DS034289,,,,,,,DOID:4049,mediastinum rhabdomyosarcoma,C1334677,,,MONDO:0002851,mediastinum rhabdomyosarcoma,
+BMGC_DS08901,BMG_DS034290,,,,,,,DOID:4050,mediastinum sarcoma,C1334678,,,MONDO:0002852,mediastinum sarcoma,
+BMGC_DS08902,BMG_DS034291,,,,,,,DOID:6175,mediastinal neurilemmoma,C1334679,,,MONDO:0004398,mediastinal schwannoma,
+BMGC_DS08903,BMG_DS034292,,,,,,,DOID:6249,mediastinum seminoma,C1334680,,,MONDO:0003826,mediastinum seminoma,
+BMGC_DS08904,BMG_DS034293,,,,,,,DOID:5488,mediastinum synovial sarcoma,C1334681,,,MONDO:0003467,mediastinum synovial sarcoma,
+BMGC_DS08905,BMG_DS034294,,,,,,,DOID:5568,mediastinum teratoma,C1334682,,,MONDO:0003518,mediastinum teratoma,
+BMGC_DS08906,BMG_DS034296,,,,,,,DOID:7206,melanomatosis,C1334691,,,MONDO:0004141,melanomatosis,
+BMGC_DS08907,BMG_DS034297,,,,,,,DOID:3565;DOID:0080843,meningioma | supratentorial meningioma,C1334698,,,,,
+BMGC_DS08908,BMG_DS034298,,,,,,,DOID:3350,mesenchymal cell neoplasm,C1334699,,,MONDO:0002616,mesenchymal cell neoplasm,
+BMGC_DS08909,BMG_DS034299,,,,,,,DOID:3379,metachronous osteosarcoma of the bone,C1334704,,,MONDO:0002632,metachronous osteosarcoma of the bone,
+BMGC_DS08910,BMG_DS034300,,,,,,,DOID:5178,metachronous kidney Wilms' tumor,C1334705,,,MONDO:0003317,metachronous kidney Wilms' tumor,
+BMGC_DS08911,BMG_DS034301,,,,,,,DOID:4680,breast metaplastic carcinoma,C1334708,,,MONDO:0006043,metaplastic breast carcinoma,
+BMGC_DS08912,BMG_DS034302,,,,,,,DOID:7379,adrenal medulla carcinoma,C1334717,,,MONDO:0024868,metastatic carcinoma in the adrenal medulla,
+BMGC_DS08913,BMG_DS034303,,,,,,,DOID:5821,methotrexate-associated lymphoproliferation,C1334749,,,MONDO:0019483,methotrexate-associated lymphoproliferative disorders,
+BMGC_DS08914,BMG_DS034304,,,,,,,DOID:8335,microglandular adenosis of breast,C1334753,,,MONDO:0004534,microglandular adenosis of breast,
+BMGC_DS08915,BMG_DS034305,,,,,,,DOID:4749,middle cranial fossa meningioma,C1334757,,,MONDO:0003121,middle cranial fossa meningioma,
+BMGC_DS08916,BMG_DS034306,,,,,,,DOID:4892,middle ear adenocarcinoma,C1334758,,,MONDO:0003189,middle ear adenocarcinoma,
+BMGC_DS08917,BMG_DS034308,,,,,,,DOID:4893,middle ear carcinoma,C1334760,,,MONDO:0003190,middle ear carcinoma,
+BMGC_DS08918,BMG_DS034309,,,,,,,DOID:5526,middle ear squamous cell carcinoma,C1334762,,,MONDO:0006303,middle ear squamous cell carcinoma,
+BMGC_DS08919,BMG_DS034313,,,,,,,DOID:6522,mixed cell uveal melanoma,C1334782,,,MONDO:0003910,mixed cell uveal melanoma,
+BMGC_DS08920,BMG_DS034314,,,,,,,DOID:5789,mixed hepatoblastoma,C1334784,,,MONDO:0003650,mixed hepatoblastoma,
+BMGC_DS08921,BMG_DS034316,,,,,,,DOID:7081,lung mixed small cell and squamous cell carcinoma,C1334788,,,MONDO:0004100,lung mixed small cell and squamous cell carcinoma,
+BMGC_DS08922,BMG_DS034317,,,,,,,DOID:5495,monophasic synovial sarcoma,C1334801,,,MONDO:0005067,monophasic synovial sarcoma,
+BMGC_DS08923,BMG_DS034318,,,,,,,DOID:3610,breast mucinous carcinoma,C1334807,,,MONDO:0002707,breast mucinous carcinoma,
+BMGC_DS08924,BMG_DS034319,,,,,,,DOID:3716,mucinous stomach adenocarcinoma,C1334809,,,MONDO:0006309,mucinous gastric adenocarcinoma,
+BMGC_DS08925,BMG_DS034321,,,,,,,DOID:4679,breast mucoepidermoid carcinoma,C1334813,,,MONDO:0003087,mucoepidermoid breast carcinoma,
+BMGC_DS08926,BMG_DS034322,,,,,,,DOID:4678,thymus mucoepidermoid carcinoma,C1334814,,,MONDO:0003086,thymic mucoepidermoid carcinoma,
+BMGC_DS08927,BMG_DS034323,,,,,,,DOID:0111152,multicentric Castleman disease,C1334815,,,MONDO:0019754,multicentric Castleman disease,
+BMGC_DS08928,BMG_DS034324,,,,,,,DOID:7086,multicentric papillary thyroid carcinoma,C1334817,,,MONDO:0004101,multicentric papillary thyroid carcinoma,
+BMGC_DS08929,BMG_DS034326,,,,,,,DOID:3360,multifocal osteogenic sarcoma,C1334820,,,MONDO:0002622,multifocal osteogenic sarcoma,
+BMGC_DS08930,BMG_DS034327,,,,,,,DOID:7646,multiple spinal canal and spinal cord meningioma,C1334825,,,MONDO:0004317,multiple spinal canal and spinal cord meningioma,
+BMGC_DS08931,BMG_DS034328,,,,,,,DOID:5155,multiple mucosal neuroma,C1334828,,,MONDO:0003307,multiple mucosal neuroma,
+BMGC_DS08932,BMG_DS034329,,,,,,,DOID:7054,multiple skull base meningioma,C1334829,,,MONDO:0004094,multiple skull base meningioma,
+BMGC_DS08933,BMG_DS034330,,,,,,,DOID:4930,nasal cavity adenocarcinoma,C1334920,,,MONDO:0003211,nasal cavity adenocarcinoma,
+BMGC_DS08934,BMG_DS034331,,,,,,,DOID:10813,nasal cavity lymphoma,C1334921,,,MONDO:0001130,nasal cavity lymphoma,
+BMGC_DS08935,BMG_DS034332,,,,,,,DOID:10812,nasal cavity olfactory neuroblastoma,C1334923,,,MONDO:0001129,nasal cavity olfactory neuroblastoma,
+BMGC_DS08936,BMG_DS034334,,,,,,,DOID:1542,head and neck carcinoma,C1334927,,,,,
+BMGC_DS08937,BMG_DS034336,,,,,,,DOID:4693,nerve plexus neoplasm,C1334945,,,MONDO:0003100,nerve plexus neoplasm,
+BMGC_DS08938,BMG_DS034337,,,,,,,DOID:4698,nerve root neoplasm,C1334946,,,MONDO:0003103,nerve root neoplasm,
+BMGC_DS08939,BMG_DS034339,,,,,,,DOID:3093,nervous system cancer,C1334956,,,,,
+BMGC_DS08940,BMG_DS034340,,,,,,,DOID:5048,posterior pituitary gland neoplasm,C1334957,,,MONDO:0003257,posterior pituitary gland neoplasm,
+BMGC_DS08941,BMG_DS034341,,,,,,,DOID:6629,nipple carcinoma,C1334966,,,MONDO:0003950,nipple carcinoma,
+BMGC_DS08942,BMG_DS034342,,,,,,,DOID:7953,nipple duct carcinoma,C1334967,,,MONDO:0004409,nipple duct carcinoma,
+BMGC_DS08943,BMG_DS034345,,,,,,,DOID:3873,desmoplastic/nodular medulloblastoma,C1334970,,,MONDO:0016710,medulloblastoma with extensive nodularity,
+BMGC_DS08944,BMG_DS034347,,,,,,,DOID:7698,non-functioning pancreatic endocrine tumor,C1334977,,,MONDO:0004334,non-functional pancreatic neuroendocrine tumor,
+BMGC_DS08945,BMG_DS034348,,,,,,,DOID:5907,penis non-invasive verrucous carcinoma,C1334984,,,MONDO:0003697,non-invasive verrucous carcinoma of the penis,
+BMGC_DS08946,BMG_DS034349,,,,,,,DOID:574,peripheral nervous system disease,C1335029,,,,,
+BMGC_DS08947,BMG_DS034350,,,,,,,DOID:15,reproductive system disease,C1335037,,,,,
+BMGC_DS08948,BMG_DS034351,,,,,,,DOID:18,urinary system disease,C1335051,,,,,
+BMGC_DS08949,BMG_DS034353,,,,,,,DOID:3910,lung adenocarcinoma,C1335060,,,,,
+BMGC_DS08950,BMG_DS034354,,,,,,,DOID:4560,non specific chronic endometritis,C1335061,,,MONDO:0003051,non specific chronic endometritis,
+BMGC_DS08951,BMG_DS034355,,,,,,,DOID:5176,renal Wilms' tumor,C1335062,,,MONDO:0003316,nonanaplastic kidney Wilms tumor,
+BMGC_DS08952,BMG_DS034356,,,,,,,DOID:8305,nonossifying fibromyxoid tumor,C1335063,,,MONDO:0004529,non-ossifying fibromyxoid tumor,
+BMGC_DS08953,BMG_DS034357,,,,,,,DOID:3303,notochordal cancer,C1335069,,,MONDO:0002597,notochordal tumor,
+BMGC_DS08954,BMG_DS034358,,,,,,,DOID:7169,lung occult large cell carcinoma,C1335095,,,MONDO:0004128,lung occult large cell carcinoma,
+BMGC_DS08955,BMG_DS034359,,,,,,,DOID:7168,lung occult adenocarcinoma,C1335096,,,MONDO:0004127,lung occult adenocarcinoma,
+BMGC_DS08956,BMG_DS034360,,,,,,,DOID:5414,lung occult small cell carcinoma,C1335099,,,MONDO:0003437,occult small cell lung carcinoma,
+BMGC_DS08957,BMG_DS034361,,,,,,,DOID:6510,lung occult squamous cell carcinoma,C1335100,,,MONDO:0003904,lung occult squamous cell carcinoma,
+BMGC_DS08958,BMG_DS034362,,,,,,,DOID:8057,olfactory groove meningioma,C1335107,,,MONDO:0004446,olfactory groove meningioma,
+BMGC_DS08959,BMG_DS034364,,,,,,,DOID:4991,optic nerve astrocytoma,C1335114,,,MONDO:0003234,optic nerve astrocytoma,
+BMGC_DS08960,BMG_DS034365,,,,,,,DOID:4384,orbit alveolar rhabdomyosarcoma,C1335126,,,MONDO:0002978,orbit alveolar rhabdomyosarcoma,
+BMGC_DS08961,BMG_DS034366,,,,,,,DOID:3258,orbit embryonal rhabdomyosarcoma,C1335127,,,MONDO:0002579,orbit embryonal rhabdomyosarcoma,
+BMGC_DS08962,BMG_DS034367,,,,,,,DOID:14459,hemangioma of orbit,C1335128,,,MONDO:0001974,hemangioma of orbit,
+BMGC_DS08963,BMG_DS034368,,,,,,,DOID:9987,orbit sarcoma,C1335131,,,MONDO:0004943,orbit sarcoma,
+BMGC_DS08964,BMG_DS034371,,,,,,,DOID:7787,breast osteosarcoma,C1335149,,,MONDO:0004360,breast extraskeletal osteosarcoma,
+BMGC_DS08965,BMG_DS034373,,,,,,,DOID:4527,ovarian angiosarcoma,C1335152,,,MONDO:0003035,ovarian angiosarcoma,
+BMGC_DS08966,BMG_DS034374,,,,,,,DOID:5118,ovarian cystic teratoma,C1335155,,,MONDO:0003281,ovarian cystic teratoma,
+BMGC_DS08967,BMG_DS034376,,,,,,,DOID:6212,ovarian endometrial cancer,C1335159,,,,,
+BMGC_DS08968,BMG_DS034377,,,,,,,DOID:5263,ovary leiomyosarcoma,C1335163,,,MONDO:0003355,ovary leiomyosarcoma,
+BMGC_DS08969,BMG_DS034378,,,,,,,DOID:5697,liposarcoma of the ovary,C1335165,,,MONDO:0003589,liposarcoma of the ovary,
+BMGC_DS08970,BMG_DS034379,,,,,,,DOID:3606,ovarian mucinous adenocarcinoma,C1335167,,,MONDO:0005601,ovarian mucinous adenocarcinoma,
+BMGC_DS08971,BMG_DS034380,,,,,,,DOID:6067,ovarian mucinous neoplasm,C1335168,,,MONDO:0003756,ovarian mucinous neoplasm,
+BMGC_DS08972,BMG_DS034381,,,,,,,DOID:4115,ovarian mesodermal adenosarcoma,C1335169,,,MONDO:0002880,ovarian adenosarcoma,
+BMGC_DS08973,BMG_DS034382,,,,,,,DOID:8023,myxoid liposarcoma of the ovary,C1335170,,,MONDO:0004436,ovarian myxoid liposarcoma,
+BMGC_DS08974,BMG_DS034383,,,,,,,DOID:3002,ovary neuroendocrine neoplasm,C1335172,,,MONDO:0002481,ovarian neuroendocrine neoplasm,
+BMGC_DS08975,BMG_DS034384,,,,,,,DOID:4555,ovarian large-cell neuroendocrine carcinoma,C1335174,,,MONDO:0003049,ovarian large-cell neuroendocrine carcinoma,
+BMGC_DS08976,BMG_DS034385,,,,,,,DOID:6405,ovarian papillary cystadenoma,C1335175,,,MONDO:0003872,ovarian papillary cystadenoma,
+BMGC_DS08977,BMG_DS034386,,,,,,,DOID:4059,ovary rhabdomyosarcoma,C1335176,,,MONDO:0002858,ovary rhabdomyosarcoma,
+BMGC_DS08978,BMG_DS034387,,,,,,,DOID:5744,ovary serous adenocarcinoma,C1335177,,,MONDO:0005211,ovarian serous adenocarcinoma,
+BMGC_DS08979,BMG_DS034388,,,,,,,DOID:6408,ovary papillary carcinoma,C1335178,,,MONDO:0003874,ovarian serous surface papillary adenocarcinoma,
+BMGC_DS08980,BMG_DS034389,,,,,,,DOID:6315,ovarian solid teratoma,C1335181,,,MONDO:0003852,ovarian solid teratoma,
+BMGC_DS08981,BMG_DS034390,,,,,,,DOID:6407,ovarian surface papilloma,C1335183,,,MONDO:0003873,ovarian surface papilloma,
+BMGC_DS08982,BMG_DS034391,,,,,,,DOID:4000,ovary transitional cell carcinoma,C1335184,,,MONDO:0006343,ovarian transitional cell carcinoma,
+BMGC_DS08983,BMG_DS034393,,,,,,,DOID:5637,pancreatic adenosquamous carcinoma,C1335299,,,MONDO:0005614,pancreatic adenosquamous carcinoma,
+BMGC_DS08984,BMG_DS034394,,,,,,,DOID:7697,pancreatic ACTH hormone producing tumor,C1335300,,,MONDO:0004333,pancreatic ACTH-producing neuroendocrine tumor,
+BMGC_DS08985,BMG_DS034395,,,,,,,DOID:4433,pancreatic delta cell neoplasm,C1335301,,,MONDO:0002994,pancreatic delta cell neuroendocrine tumor,
+BMGC_DS08986,BMG_DS034396,,,,,,,DOID:3498,pancreatic ductal adenocarcinoma,C1335302,,,MONDO:0005184,pancreatic ductal adenocarcinoma,
+BMGC_DS08987,BMG_DS034397,,,,,,,DOID:7577,pancreatic foamy gland adenocarcinoma,C1335303,,,MONDO:0004287,pancreatic foamy gland adenocarcinoma,
+BMGC_DS08988,BMG_DS034398,,,,,,,DOID:7574,pancreatic intraductal papillary-colloid carcinoma,C1335304,,,MONDO:0004285,pancreatic intraductal papillary-mucinous carcinoma,
+BMGC_DS08989,BMG_DS034399,,,,,,,DOID:1792,pancreas lymphoma,C1335307,,,MONDO:0002114,pancreas lymphoma,
+BMGC_DS08990,BMG_DS034400,,,,,,,DOID:7735,pancreatic colloid cystadenoma,C1335309,,,MONDO:0018523,pancreatic mucinous cystadenoma,
+BMGC_DS08991,BMG_DS034401,,,,,,,DOID:13313,pancreatic mucinous ductal ectasia,C1335310,,,MONDO:0001683,pancreatic mucinous ductal ectasia,
+BMGC_DS08992,BMG_DS034402,,,,,,,DOID:7840,pancreatic non-functioning delta cell tumor,C1335311,,,MONDO:0004377,pancreatic non-functioning delta cell tumor,
+BMGC_DS08993,BMG_DS034403,,,,,,,DOID:5751,pancreatic serous cystadenocarcinoma,C1335315,,,MONDO:0003630,pancreatic serous cystadenocarcinoma,
+BMGC_DS08994,BMG_DS034404,,,,,,,DOID:3917,pancreatic serous cystadenoma,C1335316,,,MONDO:0002808,pancreatic serous cystadenoma,
+BMGC_DS08995,BMG_DS034405,,,,,,,DOID:3497,pancreatic signet ring cell adenocarcinoma,C1335317,,,MONDO:0002666,pancreatic signet ring cell adenocarcinoma,
+BMGC_DS08996,BMG_DS034406,,,,,,,DOID:8013,penis papillary carcinoma,C1335322,,,MONDO:0004433,papillary carcinoma of the penis,
+BMGC_DS08997,BMG_DS034408,,,,,,,DOID:5588,lung papillary adenocarcinoma,C1335325,,,MONDO:0006049,papillary lung adenocarcinoma,
+BMGC_DS08998,BMG_DS034409,,,,,,,DOID:5595,papillary thymic adenocarcinoma,C1335327,,,MONDO:0003534,papillary thymic adenocarcinoma,
+BMGC_DS08999,BMG_DS034411,,,,,,,DOID:5433,urinary tract papillary transitional cell benign neoplasm,C1335329,,,MONDO:0003443,papillary urothelial neoplasm,
+BMGC_DS09000,BMG_DS034412,,,,,,,DOID:0050619,paranasal sinus cancer,C1335336,,,,,
+BMGC_DS09001,BMG_DS034413,,,,,,,DOID:0050619,paranasal sinus cancer,C1335337,,,MONDO:0006352,paranasal sinus adenoid cystic carcinoma,
+BMGC_DS09002,BMG_DS034414,,,,,,,DOID:1355,paranasal sinus lymphoma,C1335339,,,MONDO:0001743,paranasal sinus lymphoma,
+BMGC_DS09003,BMG_DS034415,,,,,,,DOID:0050619,paranasal sinus cancer,C1335340,,,MONDO:0044956,paranasal sinus mucoepidermoid carcinoma,
+BMGC_DS09004,BMG_DS034416,,,,,,,DOID:1362,paranasal sinus sarcoma,C1335342,,,MONDO:0001758,paranasal sinus sarcoma,
+BMGC_DS09005,BMG_DS034418,,,,,,,DOID:10207,paratesticular lipoma,C1335348,,,MONDO:0000976,paratesticular lipoma,
+BMGC_DS09006,BMG_DS034420,,,,,,,DOID:7611,parathyroid oncocytic adenoma,C1335351,,,MONDO:0004305,parathyroid oncocytic adenoma,
+BMGC_DS09007,BMG_DS034421,,,,,,,DOID:7284,Skene gland carcinoma,C1335352,,,,,
+BMGC_DS09008,BMG_DS034427,,,,,,,DOID:8632,Kaposi's sarcoma,C1335372,,,,,
+BMGC_DS09009,BMG_DS034428,,,,,,,DOID:8110,periampullary adenocarcinoma,C1335377,,,MONDO:0004465,periampullary adenocarcinoma,
+BMGC_DS09010,BMG_DS034430,,,,,,,DOID:6201,pericardial mesothelioma,C1335381,,,MONDO:0003805,malignant pericardial mesothelioma,
+BMGC_DS09011,BMG_DS034432,,,,,,,DOID:8030,periocular meningioma,C1335383,,,MONDO:0004439,periocular meningioma,
+BMGC_DS09012,BMG_DS034433,,,,,,,DOID:5195,peripheral nervous system ganglioneuroblastoma,C1335387,,,MONDO:0003327,peripheral ganglioneuroblastoma,
+BMGC_DS09013,BMG_DS034434,,,,,,,DOID:8225,microscopic breast papilloma,C1335390,,,MONDO:0004506,microscopic breast papilloma,
+BMGC_DS09014,BMG_DS034435,,,,,,,DOID:3316,perivascular tumor,C1335392,,,MONDO:0002604,pericytic neoplasm,
+BMGC_DS09015,BMG_DS034436,,,,,,,DOID:7818,petroclival meningioma,C1335395,,,MONDO:0004367,petroclival meningioma,
+BMGC_DS09016,BMG_DS034437,,,,,,,DOID:7482,petrous apex meningioma,C1335396,,,MONDO:0004238,petrous apex meningioma,
+BMGC_DS09017,BMG_DS034442,,,,,,,DOID:5553,pineal region choriocarcinoma,C1335414,,,MONDO:0003509,pineal region choriocarcinoma,
+BMGC_DS09018,BMG_DS034443,,,,,,,DOID:5510,pineal dysgerminoma,C1335415,,,MONDO:0003480,pineal region dysgerminoma,
+BMGC_DS09019,BMG_DS034444,,,,,,,DOID:6858,pineal region immature teratoma,C1335416,,,MONDO:0004017,pineal region immature teratoma,
+BMGC_DS09020,BMG_DS034445,,,,,,,DOID:6857,pineal region mature teratoma,C1335417,,,MONDO:0004016,pineal region mature teratoma,
+BMGC_DS09021,BMG_DS034446,,,,,,,DOID:8031,pineal region meningioma,C1335418,,,MONDO:0004440,pineal region meningioma,
+BMGC_DS09022,BMG_DS034447,,,,,,,DOID:6856,pineal region teratoma,C1335419,,,MONDO:0004015,pineal region teratoma,
+BMGC_DS09023,BMG_DS034448,,,,,,,DOID:5341,pineal region yolk sac tumor,C1335420,,,MONDO:0003399,pineal region yolk sac tumor,
+BMGC_DS09024,BMG_DS034449,,,,,,,DOID:8058,pituitary stalk meningioma,C1335422,,,MONDO:0004447,pituitary stalk meningioma,
+BMGC_DS09025,BMG_DS034450,,,,,,,DOID:780,placenta disease,C1335423,,,,,
+BMGC_DS09026,BMG_DS034452,,,,,,,DOID:6564,neurilemmoma of the pleura,C1335435,,,MONDO:0003926,neurilemmoma of the pleura,
+BMGC_DS09027,BMG_DS034453,,,,,,,DOID:3688,plexopathy,C1335437,,,,,
+BMGC_DS09028,BMG_DS034454,,,,,,,DOID:6553,posterior foramen magnum meningioma,C1335449,,,MONDO:0003921,posterior foramen magnum meningioma,
+BMGC_DS09029,BMG_DS034455,,,,,,,DOID:9952,acute lymphoblastic leukemia,C1335469,,,MONDO:0003538,precursor lymphoblastic lymphoma/leukemia,
+BMGC_DS09030,BMG_DS034457,,,,,,,DOID:3371,chondrosarcoma,C1335473,,,,,
+BMGC_DS09031,BMG_DS034459,,,,,,,DOID:8006,skin meningioma,C1335481,,,MONDO:0024663,primary skin meningioma,
+BMGC_DS09032,BMG_DS034461,,,,,,,DOID:5764,lung meningioma,C1335488,,,,,
+BMGC_DS09033,BMG_DS034462,,,,,,,DOID:4868,prostate adenoid cystic carcinoma,C1335502,,,MONDO:0003177,prostate adenoid cystic carcinoma,
+BMGC_DS09034,BMG_DS034463,,,,,,,DOID:5634,adenosquamous prostate carcinoma,C1335503,,,MONDO:0003558,adenosquamous prostate carcinoma,
+BMGC_DS09035,BMG_DS034464,,,,,,,DOID:4524,prostate angiosarcoma,C1335504,,,MONDO:0003033,prostate angiosarcoma,
+BMGC_DS09036,BMG_DS034465,,,,,,,DOID:3251,prostate embryonal rhabdomyosarcoma,C1335508,,,MONDO:0002574,prostate embryonal rhabdomyosarcoma,
+BMGC_DS09037,BMG_DS034466,,,,,,,DOID:8632,Kaposi's sarcoma,C1335509,,,,,
+BMGC_DS09038,BMG_DS034468,,,,,,,DOID:5282,prostate leiomyosarcoma,C1335511,,,MONDO:0003368,prostate leiomyosarcoma,
+BMGC_DS09039,BMG_DS034469,,,,,,,DOID:10290,prostate lymphoma,C1335512,,,MONDO:0000996,prostate lymphoma,
+BMGC_DS09040,BMG_DS034470,,,,,,,DOID:3703,prostate colloid adenocarcinoma,C1335513,,,MONDO:0006067,acinar prostate mucinous adenocarcinoma,
+BMGC_DS09041,BMG_DS034471,,,,,,,DOID:2992,prostate neuroendocrine neoplasm,C1335515,,,MONDO:0002477,prostate neuroendocrine neoplasm,
+BMGC_DS09042,BMG_DS034472,,,,,,,DOID:3252,prostate rhabdomyosarcoma,C1335518,,,MONDO:0006389,prostate rhabdomyosarcoma,
+BMGC_DS09043,BMG_DS034473,,,,,,,DOID:3504,prostate signet ring cell adenocarcinoma,C1335520,,,,,
+BMGC_DS09044,BMG_DS034474,,,,,,,DOID:7152,prostate stromal sarcoma,C1335521,,,MONDO:0004124,prostate stromal sarcoma,
+BMGC_DS09045,BMG_DS034475,,,,,,,DOID:7492,central epithelioid sarcoma,C1335563,,,MONDO:0004244,proximal-type epithelioid sarcoma,
+BMGC_DS09046,BMG_DS034477,,,,,,,DOID:7389,pulmonary artery leiomyosarcoma,C1335572,,,MONDO:0004207,pulmonary artery leiomyosarcoma,
+BMGC_DS09047,BMG_DS034478,,,,,,,DOID:8007,Pancoast tumor,C1335574,,,MONDO:0024813,pulmonary sulcus neoplasm,
+BMGC_DS09048,BMG_DS034479,,,,,,,DOID:7388,pulmonary vein leiomyosarcoma,C1335575,,,MONDO:0004206,pulmonary vein leiomyosarcoma,
+BMGC_DS09049,BMG_DS034480,,,,,,,DOID:2053,reactive cutaneous fibrous lesion,C1335666,,,MONDO:0006603,reactive cutaneous fibrous lesion,
+BMGC_DS09050,BMG_DS034483,,,,,,,DOID:6190,rectum Kaposi's sarcoma,C1335681,,,MONDO:0003796,rectum Kaposi sarcoma,
+BMGC_DS09051,BMG_DS034484,,,,,,,DOID:7160,rectal leiomyoma,C1335682,,,MONDO:0004125,rectum leiomyoma,
+BMGC_DS09052,BMG_DS034485,,,,,,,DOID:5297,rectum leiomyosarcoma,C1335683,,,MONDO:0003379,rectum leiomyosarcoma,
+BMGC_DS09053,BMG_DS034486,,,,,,,DOID:6459,rectal lipoma,C1335684,,,MONDO:0003884,lipoma of the rectum,
+BMGC_DS09054,BMG_DS034487,,,,,,,DOID:1988,rectum lymphoma,C1335685,,,MONDO:0002166,rectum lymphoma,
+BMGC_DS09055,BMG_DS034488,,,,,,,DOID:5777,rectum neuroendocrine neoplasm,C1335686,,,,,
+BMGC_DS09056,BMG_DS034489,,,,,,,DOID:4053,rectum rhabdomyosarcoma,C1335687,,,MONDO:0002853,rectum rhabdomyosarcoma,
+BMGC_DS09057,BMG_DS034490,,,,,,,DOID:1995,rectum sarcoma,C1335688,,,MONDO:0002168,rectum sarcoma,
+BMGC_DS09058,BMG_DS034491,,,,,,,DOID:7356,rectum sarcomatoid carcinoma,C1335689,,,MONDO:0004196,rectal sarcomatoid carcinoma,
+BMGC_DS09059,BMG_DS034492,,,,,,,DOID:5528,rectum squamous cell carcinoma,C1335690,,,MONDO:0018515,squamous cell carcinoma of rectum,
+BMGC_DS09060,BMG_DS034494,,,,,,,DOID:712,refractory hematologic cancer,C1335724,,,MONDO:0004111,refractory hematologic cancer,
+BMGC_DS09061,BMG_DS034495,,,,,,,DOID:5287,kidney leiomyosarcoma,C1335743,,,MONDO:0003373,kidney leiomyosarcoma,
+BMGC_DS09062,BMG_DS034496,,,,,,,DOID:10194,kidney lipoma,C1335744,,,MONDO:0000968,kidney lipoma,
+BMGC_DS09063,BMG_DS034497,,,,,,,DOID:5699,kidney liposarcoma,C1335745,,,MONDO:0003591,kidney liposarcoma,
+BMGC_DS09064,BMG_DS034498,,,,,,,DOID:5983,kidney osteogenic sarcoma,C1335747,,,MONDO:0003721,kidney osteogenic sarcoma,
+BMGC_DS09065,BMG_DS034499,,,,,,,DOID:4918,renal pelvis adenocarcinoma,C1335748,,,MONDO:0003205,renal pelvis adenocarcinoma,
+BMGC_DS09066,BMG_DS034500,,,,,,,DOID:4919,renal pelvis carcinoma,C1335749,,,MONDO:0005519,renal pelvis carcinoma,
+BMGC_DS09067,BMG_DS034501,,,,,,,DOID:6118,renal pelvis inverted papilloma,C1335751,,,MONDO:0003776,renal pelvis inverted papilloma,
+BMGC_DS09068,BMG_DS034502,,,,,,,DOID:6844,kidney pelvis sarcomatoid transitional cell carcinoma,C1335752,,,MONDO:0004009,kidney pelvis sarcomatoid transitional cell carcinoma,
+BMGC_DS09069,BMG_DS034503,,,,,,,DOID:175,vascular cancer,C1335753,,,,,
+BMGC_DS09070,BMG_DS034504,,,,,,,DOID:771,retinal cell cancer,C1335765,,,MONDO:0024341,retinal cell neoplasm,
+BMGC_DS09071,BMG_DS034505,,,,,,,DOID:5874,retroperitoneal germ cell neoplasm,C1335776,,,MONDO:0003685,retroperitoneal germ cell neoplasm,
+BMGC_DS09072,BMG_DS034506,,,,,,,DOID:5373,retroperitoneal hemangiopericytoma,C1335777,,,MONDO:0003412,retroperitoneal hemangiopericytoma,
+BMGC_DS09073,BMG_DS034507,,,,,,,DOID:12339,retroperitoneal lymphoma,C1335779,,,MONDO:0001499,retroperitoneal lymphoma,
+BMGC_DS09074,BMG_DS034508,,,,,,,DOID:8203,sacral spinal canal and spinal cord meningioma,C1335893,,,MONDO:0004498,sacral spinal canal and spinal cord meningioma,
+BMGC_DS09075,BMG_DS034512,,,,,,,DOID:7958,sarcomatoid penile squamous cell carcinoma,C1335923,,,MONDO:0004410,sarcomatoid penile squamous cell carcinoma,
+BMGC_DS09076,BMG_DS034513,,,,,,,DOID:8138,thymus sarcomatoid carcinoma,C1335924,,,MONDO:0006452,thymic sarcomatoid carcinoma,
+BMGC_DS09077,BMG_DS034514,,,,,,,DOID:3197,schwannoma of twelfth cranial nerve,C1335928,,,MONDO:0002549,schwannoma of twelfth cranial nerve,
+BMGC_DS09078,BMG_DS034515,,,,,,,DOID:3204,schwannomatosis,C1335929,,,MONDO:0008075,schwannomatosis,
+BMGC_DS09079,BMG_DS034516,,,,,,,DOID:8310,sclerosing adenosis of breast,C1335931,,,MONDO:0004531,sclerosing adenosis of breast,
+BMGC_DS09080,BMG_DS034517,,,,,,,DOID:7984,sclerosing breast papilloma,C1335932,,,MONDO:0004421,sclerosing breast papilloma,
+BMGC_DS09081,BMG_DS034518,,,,,,,DOID:4278,scrotum basal cell carcinoma,C1335934,,,MONDO:0002936,scrotum basal cell carcinoma,
+BMGC_DS09082,BMG_DS034519,,,,,,,DOID:663,scrotal angioma,C1335936,,,MONDO:0003951,scrotal hemangioma,
+BMGC_DS09083,BMG_DS034520,,,,,,,DOID:6025,selective immunoglobulin deficiency disease,C1335942,,,MONDO:0003739,selective immunoglobulin deficiency disease,
+BMGC_DS09084,BMG_DS034522,,,,,,,DOID:3503,breast signet ring cell adenocarcinoma,C1335964,,,MONDO:0002671,signet ring cell breast carcinoma,
+BMGC_DS09085,BMG_DS034523,,,,,,,DOID:8025,gastric signet ring cell adenocarcinoma,C1335965,,,MONDO:0006409,signet ring cell gastric adenocarcinoma,
+BMGC_DS09086,BMG_DS034524,,,,,,,DOID:4044,skeletal muscle neoplasm,C1335971,,,MONDO:0002848,skeletal muscle neoplasm,
+BMGC_DS09087,BMG_DS034525,,,,,,,DOID:7049,basaloid squamous cell skin carcinoma,C1335973,,,MONDO:0004091,skin basaloid carcinoma,
+BMGC_DS09088,BMG_DS034526,,,,,,,DOID:8122,pseudovascular skin squamous cell carcinoma,C1335974,,,MONDO:0004469,pseudovascular skin squamous cell carcinoma,
+BMGC_DS09089,BMG_DS034527,,,,,,,DOID:4151,skull base chordoma,C1335975,,,MONDO:0002892,skull base chordoma,
+BMGC_DS09090,BMG_DS034528,,,,,,,DOID:4437,skull base meningioma,C1335976,,,MONDO:0002998,skull base meningioma,
+BMGC_DS09091,BMG_DS034529,,,,,,,DOID:5926,extrahepatic bile duct small cell adenocarcinoma,C1335979,,,MONDO:0003708,extrahepatic bile duct small cell adenocarcinoma,
+BMGC_DS09092,BMG_DS034530,,,,,,,DOID:7142,thymus small cell carcinoma,C1335980,,,MONDO:0004122,thymus small cell carcinoma,
+BMGC_DS09093,BMG_DS034534,,,,,,,DOID:6880,small bowel fibrosarcoma,C1335994,,,MONDO:0004028,small intestinal fibrosarcoma,
+BMGC_DS09094,BMG_DS034537,,,,,,,DOID:4434,small intestine neuroendocrine neoplasm,C1336005,,,MONDO:0018510,small intestine neuroendocrine neoplasm,
+BMGC_DS09095,BMG_DS034538,,,,,,,DOID:5272,small intestinal sarcoma,C1336007,,,MONDO:0003361,small intestinal sarcoma,
+BMGC_DS09096,BMG_DS034539,,,,,,,DOID:5740,small intestinal vasoactive intestinal peptide producing tumor,C1336009,,,MONDO:0003621,small intestinal vasoactive intestinal peptide producing tumor,
+BMGC_DS09097,BMG_DS034540,,,,,,,DOID:3355,fibrosarcoma,C1336021,,,,,
+BMGC_DS09098,BMG_DS034541,,,,,,,DOID:5592,breast papillary carcinoma,C1336027,,,MONDO:0044783,solid papillary breast carcinoma,
+BMGC_DS09099,BMG_DS034542,,,,,,,DOID:6827,pancreatic solid pseudopapillary carcinoma,C1336029,,,MONDO:0018525,solid pseudopapillary carcinoma of pancreas,
+BMGC_DS09100,BMG_DS034544,,,,,,,DOID:7820,sphenocavernous meningioma,C1336036,,,MONDO:0004370,sphenocavernous meningioma,
+BMGC_DS09101,BMG_DS034545,,,,,,,DOID:7678,sphenoid sinus inverted papilloma,C1336037,,,MONDO:0004326,sphenoid sinus inverted papilloma,
+BMGC_DS09102,BMG_DS034546,,,,,,,DOID:7679,sphenoid sinus Schneiderian papilloma,C1336038,,,MONDO:0004327,sphenoid sinus Schneiderian papilloma,
+BMGC_DS09103,BMG_DS034547,,,,,,,DOID:14547,sphenoid sinus squamous cell carcinoma,C1336039,,,MONDO:0001995,sphenoid sinus squamous cell carcinoma,
+BMGC_DS09104,BMG_DS034548,,,,,,,DOID:7819,sphenoorbital meningioma,C1336040,,,MONDO:0004368,sphenoorbital meningioma,
+BMGC_DS09105,BMG_DS034549,,,,,,,DOID:14150,spinal cord lymphoma,C1336044,,,MONDO:0001892,spinal cord lymphoma,
+BMGC_DS09106,BMG_DS034550,,,,,,,DOID:14151,spinal cord melanoma,C1336045,,,MONDO:0001893,spinal cord melanoma,
+BMGC_DS09107,BMG_DS034551,,,,,,,DOID:6871,spinal cord neuroblastoma,C1336046,,,MONDO:0004024,spinal cord neuroblastoma,
+BMGC_DS09108,BMG_DS034552,,,,,,,DOID:13742,neurofibroma of spinal cord,C1336047,,,MONDO:0001789,neurofibroma of spinal cord,
+BMGC_DS09109,BMG_DS034553,,,,,,,DOID:6872,spinal cord primitive neuroectodermal neoplasm,C1336048,,,MONDO:0006426,spinal cord primitive neuroectodermal tumor,
+BMGC_DS09110,BMG_DS034554,,,,,,,DOID:14152,spinal cord sarcoma,C1336049,,,MONDO:0001894,spinal cord sarcoma,
+BMGC_DS09111,BMG_DS034555,,,,,,,DOID:7824,spinal multifocal clear cell meningioma,C1336051,,,MONDO:0004371,spinal multifocal clear cell meningioma,
+BMGC_DS09112,BMG_DS034557,,,,,,,DOID:709,splenic manifestation of hairy cell leukemia,C1336064,,,MONDO:0004104,splenic manifestation of hairy cell leukemia,
+BMGC_DS09113,BMG_DS034558,,,,,,,DOID:710,splenic manifestation of leukemia,C1336065,,,MONDO:0004107,splenic manifestation of leukemia,
+BMGC_DS09114,BMG_DS034559,,,,,,,DOID:4334,splenic manifestation of prolymphocytic leukemia,C1336066,,,MONDO:0002966,splenic manifestation of prolymphocytic leukemia,
+BMGC_DS09115,BMG_DS034560,,,,,,,DOID:8029,sporadic breast cancer,C1336076,,,MONDO:0004438,sporadic breast cancer,
+BMGC_DS09116,BMG_DS034561,,,,,,,DOID:4465,papillary renal cell carcinoma,C1336078,,,,,
+BMGC_DS09117,BMG_DS034562,,,,,,,DOID:5514,breast squamous cell carcinoma,C1336079,,,MONDO:0006056,squamous cell breast carcinoma,
+BMGC_DS09118,BMG_DS034563,,,,,,,DOID:5518,penis squamous cell carcinoma,C1336081,,,,,
+BMGC_DS09119,BMG_DS034564,,,,,,,DOID:5530,thymus squamous cell carcinoma,C1336082,,,MONDO:0003493,thymus squamous cell carcinoma,
+BMGC_DS09120,BMG_DS034566,,,,,,,DOID:8275,intratubular embryonal carcinoma,C1336096,,,,,
+BMGC_DS09121,BMG_DS034567,,,,,,,DOID:7315,Jewett-Marshall bladder cancer,C1336362,,,MONDO:0004182,stage IVb bladder cancer,
+BMGC_DS09122,BMG_DS034568,,,,,,,DOID:6762,sternum lymphoma,C1336504,,,MONDO:0003988,sternum lymphoma,
+BMGC_DS09123,BMG_DS034569,,,,,,,DOID:3925,steroid lipomatosis,C1336506,,,MONDO:0006612,steroid lipomatosis,
+BMGC_DS09124,BMG_DS034574,,,,,,,DOID:7371,superficial urinary bladder cancer,C1336527,,,MONDO:0004200,superficial urinary bladder carcinoma,
+BMGC_DS09125,BMG_DS034575,,,,,,,DOID:8208,lung superior sulcus carcinoma,C1336529,,,MONDO:0004500,lung superior sulcus carcinoma,
+BMGC_DS09126,BMG_DS034576,,,,,,,DOID:4522,superior vena cava angiosarcoma,C1336530,,,MONDO:0003032,superior vena cava angiosarcoma,
+BMGC_DS09127,BMG_DS034577,,,,,,,DOID:7390,superior vena cava leiomyosarcoma,C1336531,,,MONDO:0004208,superior vena cava leiomyosarcoma,
+BMGC_DS09128,BMG_DS034578,,,,,,,DOID:7634,suprasellar meningioma,C1336535,,,MONDO:0004312,suprasellar meningioma,
+BMGC_DS09129,BMG_DS034580,,,,,,,DOID:4791,supratentorial primitive neuroectodermal tumor,C1336538,,,MONDO:0003145,supratentorial primitive neuroectodermal tumor,
+BMGC_DS09130,BMG_DS034581,,,,,,,DOID:3201,sympathetic neurilemmoma,C1336543,,,MONDO:0002554,sympathetic neurilemmoma,
+BMGC_DS09131,BMG_DS034582,,,,,,,DOID:6696,synchronous multifocal osteogenic sarcoma,C1336544,,,MONDO:0003967,synchronous multifocal osteogenic sarcoma,
+BMGC_DS09132,BMG_DS034583,,,,,,,DOID:8274,synovial angioma,C1336546,,,MONDO:0004519,synovial angioma,
+BMGC_DS09133,BMG_DS034585,,,,,,,DOID:7089,tall cell papillary thyroid carcinoma,C1336695,,,MONDO:0004103,tall cell variant thyroid gland papillary carcinoma,
+BMGC_DS09134,BMG_DS034586,,,,,,,DOID:6048,telangiectatic glomangioma,C1336699,,,MONDO:0003747,telangiectatic glomangioma,
+BMGC_DS09135,BMG_DS034587,,,,,,,DOID:7016,tendon sheath lipoma,C1336703,,,MONDO:0004076,tendon sheath lipoma,
+BMGC_DS09136,BMG_DS034588,,,,,,,DOID:5557,testicular germ cell cancer,C1336708,,273300,MONDO:0010108,testicular germ cell tumor,
+BMGC_DS09137,BMG_DS034589,,,,,,,DOID:5331,testicular granulosa cell tumor,C1336709,,,MONDO:0003395,testicular granulosa cell tumor,
+BMGC_DS09138,BMG_DS034590,,,,,,,DOID:12286,testicular leukemia,C1336711,,,MONDO:0001482,testicular leukemia,
+BMGC_DS09139,BMG_DS034591,,,,,,,DOID:4743,mixed testicular germ cell tumor,C1336720,,,MONDO:0003120,mixed testicular germ cell cancer,
+BMGC_DS09140,BMG_DS034592,,,,,,,DOID:4061,testis rhabdomyosarcoma,C1336726,,,MONDO:0002860,testis rhabdomyosarcoma,
+BMGC_DS09141,BMG_DS034593,,,,,,,DOID:4062,testis sarcoma,C1336727,,,MONDO:0002861,testis sarcoma,
+BMGC_DS09142,BMG_DS034594,,,,,,,DOID:6098,thalamic neoplasm,C1336733,,,,,
+BMGC_DS09143,BMG_DS034595,,,,,,,DOID:6103,thoracic spinal canal and spinal cord meningioma,C1336738,,,MONDO:0003770,thoracic spinal canal and spinal cord meningioma,
+BMGC_DS09144,BMG_DS034596,,,,,,,DOID:4923,thymus adenocarcinoma,C1336743,,,MONDO:0003209,thymus gland adenocarcinoma,
+BMGC_DS09145,BMG_DS034598,,,,,,,DOID:10146,thymus lymphoma,C1336745,,,MONDO:0000951,thymus lymphoma,
+BMGC_DS09146,BMG_DS034599,,,,,,,DOID:4514,thyroid angiosarcoma,C1336748,,,MONDO:0003027,thyroid gland angiosarcoma,
+BMGC_DS09147,BMG_DS034601,,,,,,,DOID:8162,thyroid Hurthle cell adenoma,C1336750,,,MONDO:0004483,thyroid gland oncocytic adenoma,
+BMGC_DS09148,BMG_DS034602,,,,,,,DOID:6203,thyroid hyalinizing trabecular adenoma,C1336751,,,MONDO:0003806,thyroid hyalinizing trabecular adenoma,
+BMGC_DS09149,BMG_DS034603,,,,,,,DOID:10011,thyroid lymphoma,C1336753,,,MONDO:0019962,thyroid lymphoma,
+BMGC_DS09150,BMG_DS034605,,,,,,,DOID:4515,thyroid sarcoma,C1336756,,,MONDO:0003028,thyroid sarcoma,
+BMGC_DS09151,BMG_DS034609,,,,,,,DOID:12001,tracheal lymphoma,C1336773,,,MONDO:0001417,tracheal lymphoma,
+BMGC_DS09152,BMG_DS034610,,,,,,,DOID:12002,trachea sarcoma,C1336774,,,MONDO:0001418,trachea sarcoma,
+BMGC_DS09153,BMG_DS034611,,,,,,,DOID:7713,tuberculum sellae meningioma,C1336829,,,MONDO:0004339,tuberculum sellae meningioma,
+BMGC_DS09154,BMG_DS034615,,,,,,,DOID:8221,upper clivus meningioma,C1336871,,,MONDO:0004503,upper clivus meningioma,
+BMGC_DS09155,BMG_DS034616,,,,,,,DOID:4938,ureter adenocarcinoma,C1336873,,,MONDO:0003216,ureter adenocarcinoma,
+BMGC_DS09156,BMG_DS034617,,,,,,,DOID:6935,ureter inverted papilloma,C1336874,,,MONDO:0004043,ureter inverted papilloma,
+BMGC_DS09157,BMG_DS034618,,,,,,,DOID:11887,ureter leiomyoma,C1336875,,,MONDO:0001399,ureter leiomyoma,
+BMGC_DS09158,BMG_DS034619,,,,,,,DOID:14489,ureteral lymphoma,C1336876,,,MONDO:0001977,ureteral lymphoma,
+BMGC_DS09159,BMG_DS034620,,,,,,,DOID:11888,schwannoma of ureter,C1336877,,,MONDO:0001400,schwannoma of ureter,
+BMGC_DS09160,BMG_DS034621,,,,,,,DOID:6886,ureter small cell carcinoma,C1336878,,,MONDO:0006482,ureter small cell carcinoma,
+BMGC_DS09161,BMG_DS034622,,,,,,,DOID:5539,ureter squamous cell carcinoma,C1336879,,,MONDO:0003502,ureter squamous cell carcinoma,
+BMGC_DS09162,BMG_DS034623,,,,,,,DOID:8108,fibroepithelial polyp of urethra,C1336884,,,MONDO:0006550,fibroepithelial polyp of urethra,
+BMGC_DS09163,BMG_DS034624,,,,,,,DOID:4910,urethra adenocarcinoma,C1336885,,,MONDO:0003200,urethra adenocarcinoma,
+BMGC_DS09164,BMG_DS034625,,,,,,,DOID:5307,urethra clear cell adenocarcinoma,C1336886,,,MONDO:0003387,urethra clear cell adenocarcinoma,
+BMGC_DS09165,BMG_DS034626,,,,,,,DOID:6934,urethra inverted papilloma,C1336887,,,MONDO:0004042,urethra inverted papilloma,
+BMGC_DS09166,BMG_DS034627,,,,,,,DOID:2142,urethra leiomyoma,C1336888,,,MONDO:0002222,urethra leiomyoma,
+BMGC_DS09167,BMG_DS034628,,,,,,,DOID:8109,nephrogenic adenoma of the urethra,C1336889,,,MONDO:0004464,nephrogenic adenoma of the urethra,
+BMGC_DS09168,BMG_DS034629,,,,,,,DOID:3750,urethra squamous cell carcinoma,C1336890,,,MONDO:0002764,urethra squamous cell carcinoma,
+BMGC_DS09169,BMG_DS034637,,,,,,,DOID:4994,adenomyoma of uterine corpus,C1336903,,,MONDO:0003237,adenomyoma of uterine corpus,
+BMGC_DS09170,BMG_DS034638,,,,,,,DOID:8188,uterine corpus choriocarcinoma,C1336904,,,MONDO:0004491,uterine corpus choriocarcinoma,
+BMGC_DS09171,BMG_DS034639,,,,,,,DOID:2870,endometrial adenocarcinoma,C1336905,,,MONDO:0006192,endometrial endometrioid adenocarcinoma,
+BMGC_DS09172,BMG_DS034640,,,,,,,DOID:7436,sarcomatoid uterine corpus endometrioid adenocarcinoma,C1336913,,,MONDO:0004220,endometrial endometrioid adenocarcinoma with spindled epithelial cells,
+BMGC_DS09173,BMG_DS034641,,,,,,,DOID:4113,uterine corpus adenosarcoma,C1336917,,,MONDO:0002878,uterine corpus adenosarcoma,
+BMGC_DS09174,BMG_DS034643,,,,,,,DOID:5283,vagina leiomyosarcoma,C1336940,,,MONDO:0003369,vagina leiomyosarcoma,
+BMGC_DS09175,BMG_DS034645,,,,,,,DOID:1910,vaginal yolk sac tumor,C1336945,,,MONDO:0002143,vaginal yolk sac tumor,
+BMGC_DS09176,BMG_DS034647,,,,,,,DOID:5908,penis verrucous carcinoma,C1336955,,,MONDO:0003698,penis verrucous carcinoma,
+BMGC_DS09177,BMG_DS034648,,,,,,,DOID:6777,villoglandular endometrial endometrioid adenocarcinoma,C1336962,,,MONDO:0003991,villoglandular endometrial endometrioid adenocarcinoma,
+BMGC_DS09178,BMG_DS034649,,,,,,,DOID:4991,optic nerve astrocytoma,C1336971,,,MONDO:0024649,optic tract astrocytoma,
+BMGC_DS09179,BMG_DS034651,,,,,,,DOID:2098,vulva adenocarcinoma,C1336975,,,MONDO:0024336,vulvar adenocarcinoma,
+BMGC_DS09180,BMG_DS034652,,,,,,,DOID:4301,vulva basal cell carcinoma,C1336977,,,MONDO:0002955,vulva basal cell carcinoma,
+BMGC_DS09181,BMG_DS034653,,,,,,,DOID:8255,vulva fibroepithelial polyp,C1336978,,,MONDO:0006620,vulva fibroepithelial polyp,
+BMGC_DS09182,BMG_DS034654,,,,,,,DOID:6944,vulvar seborrheic keratosis,C1336981,,,MONDO:0006622,vulvar seborrheic keratosis,
+BMGC_DS09183,BMG_DS034655,,,,,,,DOID:2071,vulvar squamous papilloma,C1336982,,,MONDO:0002194,vestibular papilloma,
+BMGC_DS09184,BMG_DS034656,,,,,,,DOID:3740,vulva verrucous carcinoma,C1336983,,,MONDO:0002758,vulva verrucous carcinoma,
+BMGC_DS09185,BMG_DS034659,,,,,,,DOID:5884,benign intermediate mesothelioma,C1337012,,,MONDO:0003688,well differentiated papillary mesothelioma,
+BMGC_DS09186,BMG_DS034660,,,,,,,,,C1337013,,,MONDO:0015447,differentiated thyroid carcinoma,
+BMGC_DS09187,BMG_DS034661,448286002,Xanthogranulomatous cholecystitis,,,,,DOID:9766,xanthogranulomatous cholecystitis,C1337035,C536762,,MONDO:0004875,xanthogranulomatous cholecystitis,Xanthogranulomatous cholecystitis (disorder) | Xanthogranulomatous cholecystitis
+BMGC_DS09188,BMG_DS034663,,,,,,,DOID:5343,central nervous system endodermal sinus tumor,C1337040,,,MONDO:0016739,yolk sac tumor of central nervous system,
+BMGC_DS09189,BMG_DS034665,39224005,Acute amebic dysentery without mention of abscess,,,,,,,C1363999,,,,,Acute amebiasis | Acute amoebiasis | Acute amebiasis (disorder)
+BMGC_DS09190,BMG_DS034670,,,,,,,,,C1366911,,116860,MONDO:0020724,cerebral cavernous malformation 1,
+BMGC_DS09191,BMG_DS034671,,,,,,,,,C1367420,,,MONDO:0016236,kaposiform hemangioendothelioma,
+BMGC_DS09192,BMG_DS034672,,,,,,,,,C1367536,,,MONDO:0017340,juvenile nasopharyngeal angiofibroma,
+BMGC_DS09193,BMG_DS034673,,,,,,,,,C1367654,,,MONDO:0017604,marginal zone lymphoma,
+BMGC_DS09194,BMG_DS034674,,,,,,,DOID:5591,eccrine papillary adenocarcinoma,C1367774,,,,,
+BMGC_DS09195,BMG_DS034676,,,,,,,DOID:5030,pineal parenchymal tumor of intermediate differentiation,C1367859,,,MONDO:0006369,pineal parenchymal tumor of intermediate differentiation,
+BMGC_DS09196,BMG_DS034679,,,,,,,DOID:3443,mammary Paget's disease,C1368019,,,MONDO:0021165,Paget disease,
+BMGC_DS09197,BMG_DS034680,196153002;67782005,Pulmonary insufficiency following trauma,,,,,,,C1368020,,,,,Pulmonary insufficiency following trauma | Pulmonary insufficiency following trauma (disorder) | Adult respiratory distress syndrome | Congestive atelectasis | DaNang lung | Vietnam lung | Shock lung | Post-traumatic pulmonary insufficiency | Traumatic wet lung | Adult hyaline membrane disease | Acquired respiratory distress syndrome | Pulmonary capillary leak syndrome | ARDS - Adult respiratory distress syndrome | Acute respiratory distress syndrome (disorder) | Acute respiratory distress syndrome
+BMGC_DS09198,BMG_DS034681,67782005;196151000,Pulmonary insufficiency following shock,,,,,,,C1368021,,,,,Adult respiratory distress syndrome | Congestive atelectasis | DaNang lung | Vietnam lung | Shock lung | Post-traumatic pulmonary insufficiency | Traumatic wet lung | Adult hyaline membrane disease | Acquired respiratory distress syndrome | Pulmonary capillary leak syndrome | ARDS - Adult respiratory distress syndrome | Acute respiratory distress syndrome (disorder) | Acute respiratory distress syndrome | Pulmonary insufficiency following shock | Pulmonary insufficiency following shock (disorder)
+BMGC_DS09199,BMG_DS034682,,,,,,,DOID:4432,pancreatic somatostatinoma,C1368041,,,MONDO:0002993,pancreatic somatostatinoma,
+BMGC_DS09200,BMG_DS034683,,,,,,,DOID:5580,pancreatic gastrinoma,C1368066,,,MONDO:0003525,pancreatic gastrin-producing neuroendocrine tumor,
+BMGC_DS09201,BMG_DS034686,,,,,,,DOID:2513,basal cell carcinoma,C1368295,,,,,
+BMGC_DS09202,BMG_DS034687,,,,,,,DOID:154,mixed cell type cancer,C1368354,,,MONDO:0021043,mixed neoplasm,
+BMGC_DS09203,BMG_DS034689,,,,,,,DOID:305,carcinoma,C1368683,,,MONDO:0005626,epithelial neoplasm,
+BMGC_DS09204,BMG_DS034691,,,,,,,DOID:2648,sebaceous adenoma,C1368816,,,MONDO:0002375,sebaceous adenoma,
+BMGC_DS09205,BMG_DS034692,,,,,,,,,C1368871,,,MONDO:0021079,childhood neoplasm,
+BMGC_DS09206,BMG_DS034693,,,,,,,DOID:7079,adult cystic teratoma,C1368888,,,MONDO:0004099,adult cystic teratoma,
+BMGC_DS09207,BMG_DS034695,,,,,,,DOID:2660,cystic teratoma,C1368903,,,MONDO:0002379,cystic teratoma,
+BMGC_DS09208,BMG_DS034696,,,,,,,DOID:5566,mature teratoma,C1368910,,,MONDO:0003517,mature teratoma,
+BMGC_DS09209,BMG_DS034697,,,,,,,DOID:6228,peritoneal serous papillary adenocarcinoma,C1368918,,,MONDO:0018368,primary peritoneal serous/papillary carcinoma,
+BMGC_DS09210,BMG_DS034699,,,,,,,,,C1370419,,,MONDO:0023283,ovarian granulosa cell tumor,
+BMGC_DS09211,BMG_DS034700,,,,,,,DOID:3445,scrotal carcinoma,C1370468,,,MONDO:0002650,scrotal carcinoma,
+BMGC_DS09212,BMG_DS034701,,,,,,,DOID:5504,tanycytic ependymoma,C1370500,,,MONDO:0003474,tanycytic ependymoma,
+BMGC_DS09213,BMG_DS034702,,,,,,,DOID:7233,adult central nervous system embryonal carcinoma,C1370503,,,MONDO:0004155,adult central nervous system embryonal carcinoma,
+BMGC_DS09214,BMG_DS034703,,,,,,,DOID:7867,adult central nervous system germinoma,C1370504,,,MONDO:0004383,adult central nervous system germinoma,
+BMGC_DS09215,BMG_DS034704,,,,,,,DOID:6634,adult central nervous system choriocarcinoma,C1370505,,,MONDO:0003952,adult central nervous system choriocarcinoma,
+BMGC_DS09216,BMG_DS034705,,,,,,,DOID:6015,adult central nervous system teratoma,C1370506,,,MONDO:0003731,adult central nervous system teratoma,
+BMGC_DS09217,BMG_DS034706,,,,,,,DOID:6458,cerebellar liponeurocytoma,C1370507,,,MONDO:0006131,cerebellar liponeurocytoma,
+BMGC_DS09218,BMG_DS034707,,,,,,,DOID:8368,chordoid meningioma,C1370510,,,MONDO:0004544,chordoid meningioma,
+BMGC_DS09219,BMG_DS034708,,,,,,,DOID:4697,perineurioma,C1370657,,,,,
+BMGC_DS09220,BMG_DS034709,,,,,,,DOID:4696,intraneural perineurioma,C1370658,,,MONDO:0015032,intraneural perineurioma,
+BMGC_DS09221,BMG_DS034710,,,,,,,DOID:3206,plexiform schwannoma,C1370659,,,MONDO:0002559,plexiform schwannoma,
+BMGC_DS09222,BMG_DS034711,,,,,,,DOID:5443,clear cell hidradenoma,C1370701,,,MONDO:0003447,clear cell hidradenoma,
+BMGC_DS09223,BMG_DS034713,,,,,,,DOID:4896,bile duct adenocarcinoma,C1370800,,,MONDO:0003193,bile duct adenocarcinoma,
+BMGC_DS09224,BMG_DS034714,11211003,Interstitial emphysema,,CB40.3,Interstitial emphysema,J98.2,DOID:10030,pulmonary interstitial emphysema,C1370824,,,MONDO:0000923,interstitial emphysema,Interstitial emphysema | Soft tissue emphysema | Interstitial emphysema (morphologic abnormality)
+BMGC_DS09225,BMG_DS034715,,,,,,,DOID:5690,well-differentiated liposarcoma,C1370889,,,MONDO:0005103,well-differentiated liposarcoma,
+BMGC_DS09226,BMG_DS034716,,,,,,,DOID:8233,inflammatory liposarcoma,C1370890,,,MONDO:0004510,inflammatory liposarcoma,
+BMGC_DS09227,BMG_DS034717,,,,,,,DOID:7430,childhood germ cell brain tumor,C1377598,,,MONDO:0004218,childhood germ cell brain tumor,
+BMGC_DS09228,BMG_DS034718,,,,,,,DOID:6639,childhood CNS choriocarcinoma,C1377604,,,MONDO:0003953,pediatric CNS choriocarcinoma,
+BMGC_DS09229,BMG_DS034719,,,,,,,DOID:7231,childhood CNS embryonal cell carcinoma,C1377605,,,MONDO:0004153,childhood central nervous system embryonal carcinoma,
+BMGC_DS09230,BMG_DS034721,,,,,,,DOID:5343,central nervous system endodermal sinus tumor,C1377613,,,MONDO:0003401,central nervous system endodermal sinus tumor,
+BMGC_DS09231,BMG_DS034723,,,,,,,DOID:4931,nasal cavity carcinoma,C1377785,,,MONDO:0003212,nasal cavity carcinoma,
+BMGC_DS09232,BMG_DS034724,,,,,,,DOID:6489,periosteal osteogenic sarcoma,C1377843,,,MONDO:0003895,periosteal osteogenic sarcoma,
+BMGC_DS09233,BMG_DS034725,,,,,,,DOID:6468,mucinous cystadenofibroma,C1377844,,,MONDO:0003886,mucinous cystadenofibroma,
+BMGC_DS09234,BMG_DS034726,,,,,,,DOID:5479,papillary adenofibroma,C1377850,,,MONDO:0003462,papillary adenofibroma,
+BMGC_DS09235,BMG_DS034727,,,,,,,DOID:5895,clear cell cystadenofibroma,C1377853,,,MONDO:0003693,clear cell cystadenofibroma,
+BMGC_DS09236,BMG_DS034728,,,,,,,DOID:7928,testis refractory cancer,C1377904,,,MONDO:0004401,testis refractory cancer,
+BMGC_DS09237,BMG_DS034731,,,,,,,DOID:5157,benign pleural mesothelioma,C1377913,,,MONDO:0003308,pleural mesothelioma,
+BMGC_DS09238,BMG_DS034732,,,,,,,DOID:4812,adult brainstem gliosarcoma,C1377914,,,MONDO:0003152,adult brainstem gliosarcoma,
+BMGC_DS09239,BMG_DS034733,,,,,,,DOID:5921,adult brainstem mixed glioma,C1377915,,,MONDO:0003705,adult brainstem mixed glioma,
+BMGC_DS09240,BMG_DS034735,,,,,,,,,C1378050,,553000,MONDO:0010795,oncocytic neoplasm,
+BMGC_DS09241,BMG_DS034737,,,,,,,DOID:12603,acute leukemia,C1378511,,,,,
+BMGC_DS09242,BMG_DS034738,,,,,,,DOID:4451,renal carcinoma,C1378703,,,MONDO:0005206,renal carcinoma,
+BMGC_DS09243,BMG_DS034739,,,,,,,DOID:5090,sternum cancer,C1382025,,,MONDO:0003273,sternum cancer,
+BMGC_DS09244,BMG_DS034740,,,,,,,DOID:4840,sebaceous carcinoma,C1382026,,,MONDO:0037735,sebaceous gland cancer,
+BMGC_DS09245,BMG_DS034741,,,,,,,DOID:5500,cellular ependymoma,C1384403,,,MONDO:0003470,cellular ependymoma,
+BMGC_DS09246,BMG_DS034742,,,,,,,DOID:4588,secretory meningioma,C1384406,,,MONDO:0003055,secretory meningioma,
+BMGC_DS09247,BMG_DS034743,,,,,,,DOID:4594,microcystic meningioma,C1384408,,,MONDO:0003058,microcystic meningioma,
+BMGC_DS09248,BMG_DS034744,,,,,,,DOID:7689,leptomeninges sarcoma,C1384416,,,MONDO:0004330,leptomeningeal sarcoma,
+BMGC_DS09249,BMG_DS034748,,Conn Syndrome,Hyperaldosteronism,,,,DOID:12028,Conn's syndrome,C1384514,D006929,,MONDO:0001422,primary aldosteronism,
+BMGC_DS09250,BMG_DS034749,54238005;367333009;48723006;370997001,Primary testicular failure,,,,,,,C1384582,,,,,"Primary hypogonadism | Primary failure of the testes | Primary testicular failure | Primary hypogonadism (disorder) | Primary testicular failure | Primary testicular failure (disorder) | Male hypogonadism | Eunuchoidism hypogonadism | Primary gonadal failure | Testicular hypogonadism | Eunuchoidism | Testicular failure | Primary male hypogonadism | Male hypogonadism (disorder) | Eunuchoidism, hypogonadism | Primary testicular failure (disorder) | Primary testicular failure | Primary failure of the testes"
+BMGC_DS09251,BMG_DS034750,73465006,Congenital absence of germinal epithelium of testes,,,,,DOID:0050457,Sertoli cell-only syndrome,C1384583,,,,,Congenital absence of germinal epithelium of testes | Germinal aplasia | Sertoli-cell-only syndrome | Germinal cell absence | AZF - Azoospermia factor | Azoospermia factor | Gene deletion in AZF region of Y chromosome | Congenital absence of germinal epithelium of testes (disorder)
+BMGC_DS09252,BMG_DS034753,59089002;240697008;186989008;399029005;266216007,Tinea cruris,,1F28.3,Genitocrural dermatophytosis,B35.6,,,C1384589,,,,,Tinea cruris | Tinea inguinalis | Eczema marginatum | Tinea of groin | Tinea of perianal region | Dhobie itch | Jock itch | Ringworm of genitocrural region | Tinea cruris (disorder) | Dermatophytosis of groin | Dermatophytosis of groin and pubic area | Hebrae | Dermatophytosis of groin and perianal area | Dhobie itch | Hebrae | Eczema marginatum | Tinea cruris | Dermatophytosis of groin and pubic area | Dermatophytosis of groin and pubic area (disorder) | Dhobie itch | Dermatophytosis of groin and perianal area | Tinea cruris | (Dermatophytosis of groin & perianal area) or (Dhobie itch) or (tinea cruris) | (Dermatophytosis of groin & perianal area) or (Dhobie itch) or (tinea cruris) (disorder) | Tinea cruris (disorder) | Tinea cruris | Tinea inguinalis | Eczema marginatum | Tinea cruris | Dhobie itch | Tinea of groin/perianal | (Tinea: [groin/perianal] or [cruris]) or (Dhobie itch) | (Tinea: [groin/perianal] or [cruris]) or (Dhobie itch) (disorder)
+BMGC_DS09253,BMG_DS034756,201796004,Systemic onset juvenile chronic arthritis,,,,,,,C1384600,,,,,Systemic onset juvenile chronic arthritis | Juvenile arthritis with systemic onset | Systemic onset juvenile chronic arthritis (disorder) | Systemic onset juvenile rheumatoid arthritis | Systemic juvenile idiopathic arthritis | Juvenile onset Still's disease
+BMGC_DS09254,BMG_DS034759,123796003;268074002;202656009;387800004;156622007,Cervical spondylosis,,,,,,,C1384641,,184300,MONDO:0008481,"spondylosis, cervical",Cervical spondylosis | Cervical arthritis | Cervical spondylarthritis | Cervical spondylitis | CS - Cervical spondylosis | Cervical spondyloarthritis | Cervical spine degeneration | Cervical osteoarthritis | Osteoarthritis of cervical spine | Cervical spondylosis without myelopathy | Cervical spondylosis (disorder) | (Spondyloses: [cervical] or [lumbar] or [sacral]) or (arthritis - spine) or (osteoarthritis - spine) | Lumbar spondylosis | Sacral spondylosis | Osteoarthritis of spine | Arthritis - spine | Osteoarthritis - spine | Spondyloses | Degeneration of lumbar spine | Cervical spondylosis | Arthritis of spine | (Spondyloses: [cervical] or [lumbar] or [sacral]) or (arthritis - spine) or (osteoarthritis - spine) (disorder) | Osteoarthritis cervical spine | Cervical spondylosis without myelopathy | Osteoarthritis of cervical spine | Cervical spondylosis | Cervical spondylosis (& [without myelopathy]) or (osteoarthritis cervical spine) | Cervical spondylosis (& [without myelopathy]) or (osteoarthritis cervical spine) (disorder) | Cervical spondylosis (disorder) | Cervical spondylosis | CS - Cervical spondylosis | Cervical spine degeneration | (Spondyloses: [cervical] or [lumbar] or [sacral]) or (arthritis - spine) or (osteoarthritis - spine) | Arthritis - spine | Osteoarthritis - spine | Spondyloses | Osteoarthritis of spine | Sacral spondylosis | Degeneration of lumbar spine | Cervical spondylosis | Arthritis of spine | Lumbar spondylosis | (Spondyloses: [cervical] or [lumbar] or [sacral]) or (arthritis - spine) or (osteoarthritis - spine) (disorder)
+BMGC_DS09255,BMG_DS034760,,,,,,,,,C1384666,,,MONDO:0005365,hearing loss disorder,
+BMGC_DS09256,BMG_DS034763,,,,,,,DOID:6933,bladder transitional cell papilloma,C1384678,,,MONDO:0044906,bladder urothelial papilloma,
+BMGC_DS09257,BMG_DS034773,,Cystic Disease Of Lung,,,,,,,C1384901,C563237,,,,
+BMGC_DS09258,BMG_DS034789,,Aneurysm Of Interventricular Septum,,,,,,,C1387721,C563239,105805,MONDO:0007112,interventricular septum aneurysm,
+BMGC_DS09259,BMG_DS034790,,Angiostrongylus costaricensis infection,,,,,DOID:0050256,angiostrongyliasis,C1387797,C536369,,,,
+BMGC_DS09260,BMG_DS034795,,,,,,,DOID:7540,breast apocrine adenoma,C1388299,,,MONDO:0004273,breast apocrine adenoma,
+BMGC_DS09261,BMG_DS034799,,,,,,,,,C1389018,,606215,MONDO:0859565,atrioventricular septal defect,
+BMGC_DS09262,BMG_DS034802,,Peroneal muscle atrophy,,,,,,,C1389118,,MTHU041535,,,
+BMGC_DS09263,BMG_DS034819,,Congenital cardiomyopathy,,BC43.3,Endocardial fibroelastosis,I42.4,,,C1391997,,,,,
+BMGC_DS09264,BMG_DS034840,,Intrinsic Factor Deficiency,,,,,,,C1394891,C563242,261000,MONDO:0009852,hereditary intrinsic factor deficiency,
+BMGC_DS09265,BMG_DS034847,,,,,,,,,C1395852,,174400,MONDO:0008269,polydactyly of a biphalangeal thumb,
+BMGC_DS09266,BMG_DS034872,29320008,Ectopic rhythm,,,,,,,C1399226,,,,,Ectopic rhythm | Ectopic rhythm (disorder)
+BMGC_DS09267,BMG_DS034874,,HEMIFACIAL HYPERPLASIA,,,,,,,C1399354,,133900,MONDO:0007590,hemifacial hypertrophy,
+BMGC_DS09268,BMG_DS034912,715562001,Retinitis punctata albescens (disorder),,,,,,,C1405854,,,MONDO:0018877,retinitis punctata albescens,Retinitis punctata albescens (disorder) | Retinitis punctata albescens
+BMGC_DS09269,BMG_DS034941,,,,,,,,,C1409763,,147400,MONDO:0007826,"incisors, shovel-shaped",
+BMGC_DS09270,BMG_DS034952,24988007,Mesenteric vascular insufficiency,,DD31.Z,"Chronic vascular disorders of intestine, unspecified",K55.1,,,C1412000,,,,,Mesenteric vascular insufficiency | Mesenteric vascular insufficiency (disorder)
+BMGC_DS09271,BMG_DS034954,,,,,,,DOID:5032,pineal gland cancer,C1412004,,,MONDO:0021232,pineal body neoplasm,
+BMGC_DS09272,BMG_DS034956,,,,,,,DOID:5667,sweat gland carcinoma,C1412016,,,MONDO:0005524,sweat gland carcinoma,
+BMGC_DS09273,BMG_DS034958,,,,,,,DOID:5525,anal squamous cell carcinoma,C1412036,,,MONDO:0006082,anal squamous cell carcinoma,
+BMGC_DS09274,BMG_DS034959,,,,,,,DOID:12239,anal margin squamous cell carcinoma,C1412037,,,MONDO:0001470,anal margin squamous cell carcinoma,
+BMGC_DS09275,BMG_DS034960,,Paine syndrome,,,,,,,C1412041,C538101,311400,MONDO:0010707,Paine syndrome,
+BMGC_DS09276,BMG_DS034961,,"DEAFNESS, AUTOSOMAL RECESSIVE 25",,,,,,,C1414017,,613283;613285,MONDO:0013210,autosomal recessive nonsyndromic hearing loss 25,
+BMGC_DS09277,BMG_DS034962,,"Dystonia 6, torsion",,,,,,,C1414216,C538003,602629,MONDO:0011264,torsion dystonia 6,
+BMGC_DS09278,BMG_DS034964,,"HETEROTAXY, VISCERAL, 2, AUTOSOMAL",,,,,,,C1415817,,605376;605194,MONDO:0011546,"heterotaxy, visceral, 2, autosomal",
+BMGC_DS09279,BMG_DS034965,,RETINITIS PIGMENTOSA 23,,,,,,,C1419610,,300170;300424,MONDO:0010320,retinitis pigmentosa 23,
+BMGC_DS09280,BMG_DS034966,,RETINITIS PIGMENTOSA 28,,,,,,,C1419614,,606068;613596,MONDO:0011630,retinitis pigmentosa 28,
+BMGC_DS09281,BMG_DS034968,,CONE-ROD DYSTROPHY 9,,,,,DOID:0111020,cone-rod dystrophy 9,C1423873,,602713;612775,MONDO:0013002,cone-rod dystrophy 9,
+BMGC_DS09282,BMG_DS034975,23346002,Solar dermatitis,,,,L57.8,,,C1442835,,,,,Sunburn | Solar dermatitis | Sunburn (disorder)
+BMGC_DS09283,BMG_DS034977,27712000;190969000,Hypervitaminosis D,,5B90.2,Hypervitaminosis D,E67.3,DOID:9971,hypervitaminosis D,C1442839,,,MONDO:0004937,hypervitaminosis D,Hypervitaminosis D | Vitamin D intoxication | Hypervitaminosis D (disorder) | Vitamin D excess | Vitamin D intoxication | Hypervitaminosis D | Hypervitaminosis D (disorder)
+BMGC_DS09284,BMG_DS034979,,Lumbar Osteoarthritis,"Osteoarthritis, Spine",,,,,,C1442869,D055013,,,,
+BMGC_DS09285,BMG_DS034983,,Exostoses,Exostoses,,,,DOID:203,exostosis,C1442903,D005096,MTHU027312,MONDO:0002181,exostosis,
+BMGC_DS09286,BMG_DS034987,,"Muscular Dystrophy, Cardiac Type",,,,,,,C1442927,C563247,309930,MONDO:0010675,"muscular dystrophy, cardiac type",
+BMGC_DS09287,BMG_DS034988,,"Chondrodysplasia Punctata, Autosomal Dominant",,,,,,,C1442935,C563248,118650,MONDO:0007321,autosomal dominant chondrodysplasia punctata,
+BMGC_DS09288,BMG_DS034992,41495000;856006;46795000,Actinic porokeratosis,,,,,,,C1442958,,,,,Disseminated superficial actinic porokeratosis | Actinic porokeratosis | DSAP - Disseminated superficial actinic porokeratosis | Disseminated superficial actinic porokeratosis (disorder) | Actinic keratosis | Solar keratosis | Actinic porokeratosis | Senile keratoma | Actinic keratosis (morphologic abnormality) | Keratinocytic intraepidermal neoplasia | Actinic cheilitis | Solar keratosis of lip | Actinic cheilitis (disorder)
+BMGC_DS09289,BMG_DS034993,15739006;111255008,Avascular necrosis of the capital femoral epiphysis,,,,,,,C1442965,,150600,MONDO:0007885,Legg-Calve-Perthes disease,Juvenile osteochondrosis of hip AND/OR pelvis (disorder) | Juvenile osteochondritis of hip AND/OR pelvis | Pseudocoxalgia | Legg-Calve-Perthes disease | Perthes disease | Perthes disease of hip | Aseptic necrosis of capital femoral epiphysis | Osteonecrosis of capital femoral epiphysis | Avascular necrosis of capital femoral epiphysis (disorder) | Avascular necrosis of capital femoral epiphysis
+BMGC_DS09290,BMG_DS034995,41309000,Alcoholic liver damage,,,,,,,C1442981,,,,,Alcoholic liver damage | Alcoholic liver disease | ALD - Alcoholic liver disease | Alcoholic liver damage (disorder)
+BMGC_DS09291,BMG_DS034997,360364008;367417005;69080001;18979005,"Hyperglycinemia with ketosis and leukopenia, types I and II",,,,,,,C1442992,,,,,"PCC - Propionyl-CoA carboxylase deficiency | Hyperglycinemia with ketosis AND leukopenia, types I AND/OR II | Propionyl-CoA carboxylase deficiency | Hyperglycinaemia with ketosis AND leucopenia, types I AND/OR II | Propionyl-CoA carboxylase deficiency (disorder) | Propionic acidaemia, type I | Ketotic glycinaemia, types I and II | Propionic acidaemia, type II | Hyperglycinaemia with ketosis and leucopenia, types I and II | Hyperglycinemia with ketosis and leukopenia, types I and II | Propionic acidemia, type I | Propionic acidemia, type II | Ketotic glycinemia, types I and II | Propionic acidaemia, type I | Propionic acidaemia, type II | Hyperglycinaemia with ketosis and leucopenia, types I and II | Ketotic glycinaemia, types I and II | Propionic acidemia, type I | Hyperglycinemia with ketosis and leukopenia, types I and II | Ketotic glycinemia, types I and II | Propionic acidemia, type II | Propionyl-CoA carboxylase deficiency (disorder) | Propionyl-CoA carboxylase deficiency | Propionic acidemia | Propionic acidaemia | Ketotic glycinaemia | Ketotic hyperglycinaemia | Hyperglycinaemia with ketosis and leucopenia | Hyperglycinemia with ketosis and leukopenia | Ketotic glycinemia | Ketotic hyperglycinemia | Propionic acidemia (disorder) | Propionyl-CoA carboxylase deficiency | PCC - Propionyl-CoA carboxylase deficiency | Propionic aciduria | Propionyl-CoA carboxylase deficiency | Propionyl-CoA carboxylase deficiency (disorder)"
+BMGC_DS09292,BMG_DS035009,,Carnitine Acetyltransferase Deficiency,,,,,,,C1443228,C563249,606175,MONDO:0011642,carnitine acetyltransferase deficiency,
+BMGC_DS09293,BMG_DS035035,,Chronic Q Fever,Q Fever,,,,,,C1443892,D011778,,,,
+BMGC_DS09294,BMG_DS035049,409640001,Neomycin sulfate allergy,,,,,DOID:0040067,neomycin sulfate allergic contact dermatitis,C1443961,,,,,Neomycin sulfate allergy (disorder) | Neomycin sulphate allergy | Neomycin sulfate allergy
+BMGC_DS09295,BMG_DS035115,410800006,"Juvenile idiopathic arthritis, extended oligoarthritis",,,,,,,C1444843,,,,,"Juvenile idiopathic arthritis, extended oligoarthritis (disorder) | Juvenile idiopathic arthritis, extended oligoarthritis"
+BMGC_DS09296,BMG_DS035128,,"Cardiomyopathy, Familial Idiopathic","Cardiomyopathy, Dilated",,,,,,C1449563,D002311,115200,MONDO:0007269,dilated cardiomyopathy 1A,
+BMGC_DS09297,BMG_DS035129,,CADASILM,CADASIL,,,,,,C1449626,D046589,,,,
+BMGC_DS09298,BMG_DS035130,,Sphincter of Oddi Stenosis,Sphincter of Oddi Dysfunction,,,,,,C1449630,D046628,,,,
+BMGC_DS09299,BMG_DS035131,,Gallbladder Dyskinesia,Biliary Dyskinesia,,,,,,C1449631,D001657,,,,
+BMGC_DS09300,BMG_DS035132,,Primary Peritonitis,Peritonitis,,,,,,C1449646,D010538,,,,
+BMGC_DS09301,BMG_DS035133,,Secondary Peritonitis,Peritonitis,,,,,,C1449647,D010538,,,,
+BMGC_DS09302,BMG_DS035134,,Endocrine Breast Diseases,Breast Diseases,,,,,,C1449718,D001941,,,,
+BMGC_DS09303,BMG_DS035135,,Adolescent Gynecomastia,Gynecomastia,,,,,,C1449720,D006177,,,,
+BMGC_DS09304,BMG_DS035136,,Infant Gynecomastia,Gynecomastia,,,,DOID:11603,infant gynecomastia,C1449721,D006177,,MONDO:0001323,infant gynecomastia,
+BMGC_DS09305,BMG_DS035139,,"Pseudohypoaldosteronism, Type I, Autosomal Dominant",Pseudohypoaldosteronism,,,,,,C1449842,D011546,177735,MONDO:0008329,autosomal dominant pseudohypoaldosteronism type 1,
+BMGC_DS09306,BMG_DS035140,,"Pseudohypoaldosteronism, Type I, Autosomal Recessive",Pseudohypoaldosteronism,,,,DOID:0060855,autosomal dominant pseudohypoaldosteronism type 1,C1449843,D011546,,,,
+BMGC_DS09307,BMG_DS035141,,"Pseudohypoaldosteronism, Type II",Pseudohypoaldosteronism,,,,,,C1449844,D011546,,MONDO:0019162,pseudohypoaldosteronism type 2,
+BMGC_DS09308,BMG_DS035142,,Erythematotelangiectatic Rosacea,Rosacea,,,,,,C1449852,D012393,,,,
+BMGC_DS09309,BMG_DS035143,,Papulopustular Rosacea,Rosacea,,,,,,C1449853,D012393,,,,
+BMGC_DS09310,BMG_DS035144,,Phymatous Rosacea,Rosacea,,,,,,C1449854,D012393,,,,
+BMGC_DS09311,BMG_DS035145,,Autosomal Recessive Emery-Dreifuss Muscular Dystrophy,"Muscular Dystrophy, Emery-Dreifuss",,,,,,C1450051,D020389,,,,
+BMGC_DS09312,BMG_DS035146,,Tibial Muscular Dystrophy,Distal Myopathies,,,,,,C1450052,D049310,,,,
+BMGC_DS09313,BMG_DS035153,91162000;716379000,Acute fatty liver of pregnancy,,,,,,,C1455728,C537957,,MONDO:0016573,acute fatty liver of pregnancy,Necrosis of liver of pregnancy | Necrosis of liver of pregnancy (disorder) | Acute fatty liver of pregnancy (disorder) | Acute fatty liver of pregnancy | AFLP - acute fatty liver of pregnancy | Nonalcoholic fatty liver during pregnancy
+BMGC_DS09314,BMG_DS035160,18644006,Vagotonia,,,,,,,C1455782,,,,,Increased gastric tonus | Vagotonia | Gastric hypertonus | Increased gastric tonus (finding)
+BMGC_DS09315,BMG_DS035164,,,,,,,DOID:216,dental caries,C1456145,,,MONDO:0005592,smooth surface dental caries,
+BMGC_DS09316,BMG_DS035165,,,,,,,DOID:13629,dentine erosion,C1456162,,,MONDO:0001762,dentine erosion,
+BMGC_DS09317,BMG_DS035166,,,,,,,DOID:14140,pulp erosion,C1456163,,,MONDO:0001890,pulp erosion,
+BMGC_DS09318,BMG_DS035168,,,,,,,DOID:13239,internal pathological resorption,C1456167,,,,,
+BMGC_DS09319,BMG_DS035179,91521000119104,Narcolepsy without cataplexy,,,,G47.419,,,C1456240,,,MONDO:0019371,narcolepsy without cataplexy,Narcolepsy without cataplexy | Narcolepsy without cataplexy (disorder)
+BMGC_DS09320,BMG_DS035181,423633003,Midline cystocele,,,,,DOID:14131,midline cystocele,C1456248,,,MONDO:0001886,midline cystocele,Midline cystocele (disorder) | Midline cystocele
+BMGC_DS09321,BMG_DS035182,,,,,,,DOID:12637,perineocele,C1456251,,,MONDO:0001559,perineocele,
+BMGC_DS09322,BMG_DS035183,,,,,,,DOID:11629,pelvic muscle wasting,C1456255,,,MONDO:0001327,pelvic muscle wasting,
+BMGC_DS09323,BMG_DS035187,,,,,,,DOID:13575,non-renal secondary hyperparathyroidism,C1456268,,,,,
+BMGC_DS09324,BMG_DS035190,,,,,,,DOID:251,alcohol-induced mental disorder,C1456283,,,,,
+BMGC_DS09325,BMG_DS035200,410794002,Still's disease with juvenile onset and/or adult onset,,,,,,,C1456792,,,,,Still's disease with juvenile onset and/or adult onset (disorder) | Still's disease with juvenile onset and/or adult onset | Still's disease | Still disease with juvenile onset and/or adult onset
+BMGC_DS09326,BMG_DS035202,,Ureteral Calculi,Ureteral Calculi,,,,,,C1456865,D014514,,,,
+BMGC_DS09327,BMG_DS035204,36467003,Alpha plus thalassemia,,,,,,,C1456873,,,,,Alpha plus thalassemia | Alpha plus thalassaemia | Alpha plus thalassemia (disorder) | Alpha thalassaemia 2 | Alpha thalassemia 2
+BMGC_DS09328,BMG_DS035207,190983003;267460002,Congenital hypogammaglobulinemia,,,,,DOID:14177,congenital hypogammaglobulinemia,C1457897,,,,,Bruton's agammaglobulinaemia | Congenital hypogammaglobulinaemia | Congenital sex-linked agammaglobulinaemia | Congenital X-linked agammaglobulinaemia | Bruton's agammaglobulinemia | Congenital sex-linked agammaglobulinemia | Congenital X-linked agammaglobulinemia | Congenital hypogammaglobulinemia | Hypogammaglobulinaemia: [congenital] or [agammaglobulinaemia: (Bruton's) or (congenital sex-linked & [X-linked])] | Hypogammaglobulinemia: [congenital] or [agammaglobulinemia: (Bruton's) or (congenital sex-linked & [X-linked])] | Hypogammaglobulinaemia: [congenital] or [agammaglobulinaemia: (Bruton's) or (congenital sex-linked & [X-linked])] (disorder) | Congenital hypogammaglobulinaemia | Congenital hypogammaglobulinemia | Congenital hypogammaglobulinemia (finding)
+BMGC_DS09329,BMG_DS035212,,,,,,,,,C1458155,,,MONDO:0021100,breast neoplasm,
+BMGC_DS09330,BMG_DS035218,,Testotoxicosis,"Puberty, Precocious",,,,DOID:0111545,familial male-limited precocious puberty,C1504412,D011629,,,,
+BMGC_DS09331,BMG_DS035227,21290001000004104,Stenosis of middle cerebral artery,,,,,,,C1504568,,,,,Stenosis of middle cerebral artery (disorder) | Stenosis of middle cerebral artery
+BMGC_DS09332,BMG_DS035228,,,,,,,,,C1507149,,,MONDO:0015607,partial chromosome Y deletion,
+BMGC_DS09333,BMG_DS035229,,,,,,,DOID:4231,histiocytoma,C1509147,,,MONDO:0005509,histiocytoma,
+BMGC_DS09334,BMG_DS035230,,,,,,,DOID:495,sclerosing hemangioma,C1509148,,,MONDO:0006280,lung sclerosing hemangioma,
+BMGC_DS09335,BMG_DS035232,,,,,,,DOID:9541,osteosclerotic myeloma,C1510415,,,,,
+BMGC_DS09336,BMG_DS035233,,Gait Apraxia,Gait Apraxia,,,,DOID:4260,gait apraxia,C1510417,D020235,,MONDO:0006766,gait apraxia,
+BMGC_DS09337,BMG_DS035236,,Entrapment Neuropathies,Nerve Compression Syndromes,,,,DOID:573,nerve compression syndrome,C1510429,D009408,,MONDO:0003615,nerve compression syndrome,
+BMGC_DS09338,BMG_DS035237,,Chronic Actinic Dermatitis,Photosensitivity Disorders,,,,,,C1510437,D010787,,,,
+BMGC_DS09339,BMG_DS035240,,,,,,,DOID:12960,acrocephalosyndactylia,C1510455,,,MONDO:0019796,acrocephalosyndactyly,
+BMGC_DS09340,BMG_DS035241,,Orofaciodigital Syndrome I,Orofaciodigital Syndromes,,,,DOID:0060316,orofaciodigital syndrome I,C1510460,D009958,311200,MONDO:0010702,orofaciodigital syndrome I,
+BMGC_DS09341,BMG_DS035242,,Vitamin Deficiency,Avitaminosis,,,,,,C1510471,D001361,,MONDO:0024298,vitamin deficiency disorder,
+BMGC_DS09342,BMG_DS035243,,,,,,,,,C1510472,,,MONDO:0005303,drug dependence,
+BMGC_DS09343,BMG_DS035244,31113003,Diverticulosis,Diverticulum,,,,,,C1510475,D004240,MTHU014943,,,Diverticulum | Diverticulum (morphologic abnormality)
+BMGC_DS09344,BMG_DS035245,,Neuralgic Amyotrophy,Brachial Plexus Neuritis,,,,DOID:10383,amyotrophic neuralgia,C1510479,D020968,,MONDO:0017362,neuralgic amyotrophy,
+BMGC_DS09345,BMG_DS035246,,"Cerebral Amyloid Angiopathy, Hereditary","Cerebral Amyloid Angiopathy, Familial",,,,DOID:9246,cerebral amyloid angiopathy,C1510489,D028243,,MONDO:0005620,cerebral amyloid angiopathy,
+BMGC_DS09346,BMG_DS035247,,,,,,,DOID:5389,oxyphilic adenoma,C1510502,,,MONDO:0003424,oncocytic adenoma,
+BMGC_DS09347,BMG_DS035250,,,,,,,,,C1510586,,,MONDO:0005258,autism spectrum disorder,
+BMGC_DS09348,BMG_DS035251,64593003;271737000,Absolute anemia,,,,,,,C1510654,,,,,Anemia | Anaemia | Anemia (disorder) | Anemia | Anaemia | Absolute anemia | Absolute anaemia | Anemia (disorder)
+BMGC_DS09349,BMG_DS035252,,,,,,,DOID:4422,malignant adenofibroma,C1510778,,,MONDO:0002991,adenocarcinofibroma,
+BMGC_DS09350,BMG_DS035253,,,,,,,DOID:10368,epididymis adenocarcinoma,C1510784,,,MONDO:0001017,epididymal adenocarcinoma,
+BMGC_DS09351,BMG_DS035255,,,,,,,DOID:1642,breast adenomyoepithelioma,C1510795,,,MONDO:0002066,breast adenomyoepithelioma,
+BMGC_DS09352,BMG_DS035256,,,,,,,DOID:5623,adenosquamous breast carcinoma,C1510796,,,MONDO:0003548,adenosquamous breast carcinoma,
+BMGC_DS09353,BMG_DS035257,,,,,,,DOID:5153,atypical neurofibroma,C1510961,,,MONDO:0003306,atypical neurofibroma,
+BMGC_DS09354,BMG_DS035258,,,,,,,DOID:4879,Bartholin's gland adenoid cystic carcinoma,C1511047,,,MONDO:0003187,Bartholin gland adenoid cystic carcinoma,
+BMGC_DS09355,BMG_DS035259,,,,,,,DOID:5382,Bartholin's gland adenoma,C1511048,,,MONDO:0003419,Bartholin gland adenoma,
+BMGC_DS09356,BMG_DS035260,,,,,,,DOID:6518,Bartholin's gland adenomyoma,C1511049,,,MONDO:0003909,Bartholin gland adenomyoma,
+BMGC_DS09357,BMG_DS035261,,,,,,,DOID:5630,Bartholin's gland adenosquamous carcinoma,C1511050,,,MONDO:0003555,Bartholin gland adenosquamous carcinoma,
+BMGC_DS09358,BMG_DS035262,,,,,,,DOID:7140,Bartholin's gland small cell carcinoma,C1511051,,,MONDO:0004120,Bartholin gland small cell carcinoma,
+BMGC_DS09359,BMG_DS035263,,,,,,,DOID:6961,Bartholin's gland squamous cell carcinoma,C1511052,,,MONDO:0004053,bartholin gland squamous cell carcinoma,
+BMGC_DS09360,BMG_DS035264,,,,,,,DOID:3998,Bartholin's gland transitional cell carcinoma,C1511053,,,MONDO:0002828,Bartholin gland transitional cell carcinoma,
+BMGC_DS09361,BMG_DS035265,,,,,,,DOID:7046,cervical basaloid squamous cell carcinoma,C1511063,,,MONDO:0004088,cervical basaloid carcinoma,
+BMGC_DS09362,BMG_DS035267,,,,,,,DOID:2078,chondroid syringoma of the vulva,C1511091,,,MONDO:0002199,benign mixed tumor of the vulva,
+BMGC_DS09363,BMG_DS035269,,,,,,,DOID:135,benign vaginal carcinosarcoma,C1511106,,,MONDO:0001731,benign vaginal mixed epithelial and mesenchymal neoplasm,
+BMGC_DS09364,BMG_DS035270,,,,,,,DOID:6505,vaginal spindle cell epithelioma,C1511107,,,MONDO:0003903,benign vaginal mixed tumor,
+BMGC_DS09365,BMG_DS035271,,,,,,,DOID:6210,bladder diffuse clear cell adenocarcinoma,C1511187,,,MONDO:0003810,bladder diffuse clear cell adenocarcinoma,
+BMGC_DS09366,BMG_DS035272,,,,,,,DOID:6594,bladder colonic type adenocarcinoma,C1511188,,,MONDO:0003938,bladder colonic type adenocarcinoma,
+BMGC_DS09367,BMG_DS035273,,,,,,,DOID:8097,bladder hepatoid adenocarcinoma,C1511189,,,MONDO:0004459,bladder hepatoid adenocarcinoma,
+BMGC_DS09368,BMG_DS035275,,,,,,,DOID:8096,bladder mixed adenocarcinoma,C1511192,,,MONDO:0004458,bladder mixed adenocarcinoma,
+BMGC_DS09369,BMG_DS035276,,,,,,,DOID:3710,bladder colloid adenocarcinoma,C1511193,,,MONDO:0002750,bladder colloid adenocarcinoma,
+BMGC_DS09370,BMG_DS035277,,,,,,,DOID:8051,bladder papillary clear cell adenocarcinoma,C1511196,,,MONDO:0004445,bladder papillary clear cell adenocarcinoma,
+BMGC_DS09371,BMG_DS035278,,,,,,,DOID:5432,bladder papillary transitional cell neoplasm,C1511197,,,MONDO:0003442,bladder papillary urothelial neoplasm,
+BMGC_DS09372,BMG_DS035280,,,,,,,DOID:8050,bladder tubulo-cystic clear cell adenocarcinoma,C1511203,,,MONDO:0004444,bladder tubulo-cystic clear cell adenocarcinoma,
+BMGC_DS09373,BMG_DS035281,,,,,,,DOID:7694,bladder urachal adenocarcinoma,C1511204,,,,,
+BMGC_DS09374,BMG_DS035282,,,,,,,DOID:5957,bladder urachal squamous cell carcinoma,C1511206,,,MONDO:0003714,bladder urachal squamous cell carcinoma,
+BMGC_DS09375,BMG_DS035283,,,,,,,DOID:7244,bladder urachal urothelial carcinoma,C1511207,,,MONDO:0004163,bladder urachal urothelial carcinoma,
+BMGC_DS09376,BMG_DS035284,,,,,,,DOID:3741,bladder verrucous squamous cell carcinoma,C1511208,,,MONDO:0002759,bladder verrucous carcinoma,
+BMGC_DS09377,BMG_DS035285,,,,,,,DOID:6788,vagina botryoid rhabdomyosarcoma,C1511275,,,MONDO:0003994,botryoid-type embryonal rhabdomyosarcoma of the vagina,
+BMGC_DS09378,BMG_DS035286,,,,,,,DOID:7312,breast adenomyoepithelial adenosis,C1511283,,,MONDO:0004181,breast adenomyoepithelial adenosis,
+BMGC_DS09379,BMG_DS035287,,,,,,,DOID:1637,breast angiomatosis,C1511284,,,MONDO:0002064,breast angiomatosis,
+BMGC_DS09380,BMG_DS035288,,,,,,,DOID:8130,breast columnar cell mucinous carcinoma,C1511305,,,MONDO:0004472,breast columnar cell mucinous carcinoma,
+BMGC_DS09381,BMG_DS035290,,,,,,,DOID:7538,breast ductal adenoma,C1511307,,,MONDO:0004270,breast ductal adenoma,
+BMGC_DS09382,BMG_DS035292,,,,,,,DOID:3011,breast granular cell tumor,C1511312,,,MONDO:0002487,breast granular cell tumor,
+BMGC_DS09383,BMG_DS035293,,,,,,,DOID:5370,breast hemangiopericytoma,C1511313,,,MONDO:0003411,breast hemangiopericytoma,
+BMGC_DS09384,BMG_DS035294,,,,,,,DOID:6657,breast large cell neuroendocrine carcinoma,C1511316,,,MONDO:0003959,breast large cell neuroendocrine carcinoma,
+BMGC_DS09385,BMG_DS035296,,,,,,,DOID:3609,breast mucinous cystadenocarcinoma,C1511318,,,MONDO:0002705,breast mucinous cystadenocarcinoma,
+BMGC_DS09386,BMG_DS035297,,,,,,,DOID:3004,breast myoepithelial neoplasm,C1511319,,,MONDO:0002483,breast myoepithelial tumor,
+BMGC_DS09387,BMG_DS035299,,,,,,,DOID:8259,bulbomembranous urethral cancer,C1511339,,,MONDO:0004516,bulbomembranous urethral cancer,
+BMGC_DS09388,BMG_DS035300,,,,,,,DOID:4160,differentiating neuroblastoma,C1511934,,,MONDO:0002899,differentiating neuroblastoma,
+BMGC_DS09389,BMG_DS035303,,,,,,,DOID:7266,familiar fallopian tube carcinoma,C1512418,,,MONDO:0004166,hereditary fallopian tube carcinoma,
+BMGC_DS09390,BMG_DS035304,,,,,,,DOID:6846,familial melanoma,C1512419,,,MONDO:0018961,familial melanoma,
+BMGC_DS09391,BMG_DS035306,,,,,,,DOID:7465,chronic NK-cell lymphocytosis,C1512709,,,MONDO:0004234,chronic lymphoproliferative disorder of NK-cells,
+BMGC_DS09392,BMG_DS035307,,,,,,,DOID:7600,infiltrating bladder lymphoepithelioma-like carcinoma,C1512736,,,MONDO:0004299,infiltrating bladder lymphoepithelioma-like carcinoma,
+BMGC_DS09393,BMG_DS035308,,,,,,,DOID:6476,clear cell variant infiltrating bladder urothelial carcinoma,C1512737,,,MONDO:0003889,"infiltrating bladder urothelial carcinoma, clear cell variant",
+BMGC_DS09394,BMG_DS035309,,,,,,,DOID:7967,lipid-cell variant infiltrating bladder urothelial carcinoma,C1512738,,,MONDO:0004415,lipid-cell variant infiltrating bladder urothelial carcinoma,
+BMGC_DS09395,BMG_DS035310,,,,,,,DOID:7972,lymphoma-like variant infiltrating bladder urothelial carcinoma,C1512739,,,,,
+BMGC_DS09396,BMG_DS035311,,,,,,,DOID:7971,microcystic variant infiltrating bladder urothelial carcinoma,C1512740,,,MONDO:0004418,microcystic variant infiltrating bladder urothelial carcinoma,
+BMGC_DS09397,BMG_DS035312,,,,,,,DOID:7969,nested variant infiltrating bladder urothelial carcinoma,C1512741,,,MONDO:0004417,nested variant infiltrating bladder urothelial carcinoma,
+BMGC_DS09398,BMG_DS035313,,,,,,,DOID:7968,plasmacytoid variant infiltrating bladder urothelial carcinoma,C1512742,,,MONDO:0004416,plasmacytoid variant infiltrating bladder urothelial carcinoma,
+BMGC_DS09399,BMG_DS035314,,,,,,,DOID:7553,infiltrating bladder urothelial carcinoma sarcomatoid variant,C1512743,,,MONDO:0004278,infiltrating bladder urothelial carcinoma sarcomatoid variant,
+BMGC_DS09400,BMG_DS035315,,,,,,,DOID:6845,infiltrating ureter transitional cell carcinoma,C1512750,,,MONDO:0004010,infiltrating renal pelvis/ureter urothelial carcinoma,
+BMGC_DS09401,BMG_DS035317,,,,,,,DOID:5102,inner ear cancer,C1512779,,,MONDO:0024320,inner ear neoplasm,
+BMGC_DS09402,BMG_DS035318,,,,,,,DOID:8068,intraductal breast myoepitheliosis,C1512935,,,MONDO:0004449,intraductal breast myoepitheliosis,
+BMGC_DS09403,BMG_DS035319,,,,,,,DOID:136,vaginal carcinosarcoma,C1512974,,,MONDO:0037746,malignant vaginal mixed epithelial and mesenchymal neoplasm,
+BMGC_DS09404,BMG_DS035321,,,,,,,DOID:8302,mixed endometrial stromal and smooth muscle tumor,C1513364,,,MONDO:0004526,mixed endometrial stromal and smooth muscle tumor,
+BMGC_DS09405,BMG_DS035322,,,,,,,DOID:7541,mixed epithelial/mesenchymal metaplastic breast carcinoma,C1513365,,,MONDO:0004274,mixed epithelial/mesenchymal metaplastic breast carcinoma,
+BMGC_DS09406,BMG_DS035323,,,,,,,DOID:8009,penis mixed squamous cell carcinoma,C1513369,,,MONDO:0004430,penis mixed squamous cell carcinoma,
+BMGC_DS09407,BMG_DS035324,,,,,,,DOID:7293,mucin-rich endometrial endometrioid adenocarcinoma,C1513711,,,MONDO:0004175,mucin-rich endometrial endometrioid adenocarcinoma,
+BMGC_DS09408,BMG_DS035325,,,,,,,DOID:7024,mucinous intrahepatic cholangiocarcinoma,C1513718,,,MONDO:0004078,mucinous intrahepatic cholangiocarcinoma,
+BMGC_DS09409,BMG_DS035326,,,,,,,DOID:4472,mucinous tubular and spindle renal cell carcinoma,C1513719,,,,,
+BMGC_DS09410,BMG_DS035327,,,,,,,DOID:4687,thyroid gland mucoepidermoid carcinoma,C1513721,,,MONDO:0006463,thyroid gland mucoepidermoid carcinoma,
+BMGC_DS09411,BMG_DS035329,,,,,,,DOID:7521,breast myoepitheliosis,C1513799,,,MONDO:0004262,breast myoepitheliosis,
+BMGC_DS09412,BMG_DS035331,,,,,,,DOID:6774,polyembryoma of the ovary,C1514199,,,MONDO:0003989,polyembryoma of the ovary,
+BMGC_DS09413,BMG_DS035332,,,,,,,DOID:8042,testis polyembryoma,C1514200,,,MONDO:0004442,testis polyembryoma,
+BMGC_DS09414,BMG_DS035333,,,,,,,DOID:4500,hypokalemia,C1514284,,,MONDO:0003019,potassium deficiency disease,
+BMGC_DS09415,BMG_DS035334,,,,,,,DOID:3068,glioblastoma,C1514422,,,,,
+BMGC_DS09416,BMG_DS035335,,,,,,,DOID:1791,peritoneal carcinoma,C1514428,,,MONDO:0015686,primary peritoneal carcinoma,
+BMGC_DS09417,BMG_DS035336,,,,,,,DOID:4901,peritoneal serous adenocarcinoma,C1514429,,,MONDO:0006386,primary peritoneal serous adenocarcinoma,
+BMGC_DS09418,BMG_DS035339,,,,,,,DOID:6166,prostatic urethra urothelial carcinoma,C1514522,,,MONDO:0003790,prostatic urethra urothelial carcinoma,
+BMGC_DS09419,BMG_DS035340,,,,,,,DOID:6167,prostatic urethral cancer,C1514523,,,MONDO:0003791,prostatic urethral cancer,
+BMGC_DS09420,BMG_DS035341,,,,,,,DOID:4087,testicular pure germ cell tumor,C1514608,,,MONDO:0002874,testicular pure germ cell tumor,
+BMGC_DS09421,BMG_DS035342,,,,,,,DOID:6119,renal pelvis urothelial papilloma,C1514844,,,MONDO:0003777,renal pelvis urothelial papilloma,
+BMGC_DS09422,BMG_DS035343,,,,,,,DOID:6837,rete ovarii adenoma,C1514905,,,MONDO:0004005,rete ovarii adenoma,
+BMGC_DS09423,BMG_DS035344,,,,,,,DOID:6838,rete ovarii cystadenofibroma,C1514906,,,MONDO:0004006,rete ovarii cystadenofibroma,
+BMGC_DS09424,BMG_DS035345,,,,,,,DOID:5725,rete ovarii cystadenoma,C1514907,,,MONDO:0003610,rete ovarii cystadenoma,
+BMGC_DS09425,BMG_DS035346,,,,,,,DOID:4895,rete ovarii benign neoplasm,C1514909,,,MONDO:0003192,rete ovarii neoplasm,
+BMGC_DS09426,BMG_DS035348,,,,,,,DOID:5639,rete testis neoplasm,C1514912,,,MONDO:0003562,rete testis neoplasm,
+BMGC_DS09427,BMG_DS035350,,,,,,,DOID:3038,submucosal invasive colon adenocarcinoma,C1515024,,,MONDO:0002496,submucosal invasive colon adenocarcinoma,
+BMGC_DS09428,BMG_DS035351,,,,,,,DOID:6742,synchronous bilateral breast carcinoma,C1515107,,,MONDO:0003983,synchronous bilateral breast carcinoma,
+BMGC_DS09429,BMG_DS035352,,,,,,,DOID:7962,tamoxifen-related endometrial lesion,C1515212,,,MONDO:0004414,tamoxifen-related endometrial lesion,
+BMGC_DS09430,BMG_DS035353,,,,,,,DOID:4739,testicular Brenner tumor,C1515281,,,MONDO:0003118,testicular Brenner tumor,
+BMGC_DS09431,BMG_DS035356,,,,,,,DOID:8394,adult type testicular granulosa cell tumor,C1515284,,,MONDO:0004548,adult type testicular granulosa cell tumor,
+BMGC_DS09432,BMG_DS035357,,,,,,,DOID:6032,juvenile type testicular granulosa cell tumor,C1515285,,,MONDO:0003741,juvenile type testicular granulosa cell tumor,
+BMGC_DS09433,BMG_DS035358,,,,,,,DOID:4756,testicular Leydig cell tumor,C1515288,,,MONDO:0003737,malignant testicular Leydig cell tumor,
+BMGC_DS09434,BMG_DS035359,,,,,,,DOID:4757,testicular sex cord-stromal neoplasm,C1515289,,,,,
+BMGC_DS09435,BMG_DS035360,,,,,,,DOID:6693,testicular monophasic choriocarcinoma,C1515290,,,MONDO:0003966,testicular monophasic choriocarcinoma,
+BMGC_DS09436,BMG_DS035361,,,,,,,DOID:7269,cribriform variant testicular seminoma,C1515292,,,MONDO:0004168,cribriform variant testicular seminoma,
+BMGC_DS09437,BMG_DS035362,,,,,,,DOID:8358,pseudoglandular variant testicular seminoma,C1515293,,,MONDO:0004541,pseudoglandular variant testicular seminoma,
+BMGC_DS09438,BMG_DS035363,,,,,,,DOID:6706,tubular variant testicular seminoma,C1515294,,,MONDO:0003973,tubular variant testicular seminoma,
+BMGC_DS09439,BMG_DS035365,,,,,,,DOID:4084,testicular trophoblastic tumor,C1515301,,,MONDO:0002871,testicular trophoblastic tumor,
+BMGC_DS09440,BMG_DS035366,,,,,,,DOID:7302,endodermal sinus pattern testicular yolk sac tumor,C1515303,,,MONDO:0004178,"testicular yolk sac tumor, endodermal sinus pattern",
+BMGC_DS09441,BMG_DS035367,,,,,,,DOID:8362,enteric pattern testicular yolk sac tumor,C1515304,,,MONDO:0004543,enteric pattern testicular yolk sac tumor,
+BMGC_DS09442,BMG_DS035368,,,,,,,DOID:7930,glandular-alveolar pattern testicular yolk sac tumor,C1515305,,,MONDO:0004402,"testicular yolk sac tumor, glandular-alveolar pattern",
+BMGC_DS09443,BMG_DS035369,,,,,,,DOID:8195,hepatoid pattern testicular yolk sac tumor,C1515306,,,MONDO:0004494,"testicular yolk sac tumor, hepatoid pattern",
+BMGC_DS09444,BMG_DS035370,,,,,,,DOID:7097,macrocystic pattern testicular yolk sac tumor,C1515307,,,MONDO:0004106,"testicular yolk sac tumor, macrocystic pattern",
+BMGC_DS09445,BMG_DS035371,,,,,,,DOID:8392,reticular pattern testicular yolk sac tumor,C1515308,,,MONDO:0004547,reticular pattern testicular yolk sac tumor,
+BMGC_DS09446,BMG_DS035372,,,,,,,DOID:8081,myxomatous pattern testicular yolk sac tumor,C1515309,,,MONDO:0004453,"testicular yolk sac tumor, myxomatous pattern",
+BMGC_DS09447,BMG_DS035373,,,,,,,DOID:8193,papillary pattern testicular yolk sac tumor,C1515310,,,MONDO:0004493,"testicular yolk sac tumor, papillary pattern",
+BMGC_DS09448,BMG_DS035374,,,,,,,DOID:7435,polyvesicular vitelline pattern testicular yolk sac tumor,C1515311,,,MONDO:0004219,polyvesicular vitelline pattern testicular yolk sac tumor,
+BMGC_DS09449,BMG_DS035375,,,,,,,DOID:7360,solid pattern testicular yolk sac tumor,C1515312,,,MONDO:0004198,"testicular yolk sac tumor, solid pattern",
+BMGC_DS09450,BMG_DS035376,,,,,,,DOID:7246,lymphoepithelioma-like acinar prostate adenocarcinoma,C1515864,,,,,
+BMGC_DS09451,BMG_DS035377,,,,,,,DOID:5743,acinic cell breast carcinoma,C1515868,,,MONDO:0003624,acinic cell breast carcinoma,
+BMGC_DS09452,BMG_DS035378,,,,,,,DOID:6848,adult vagina botryoid rhabdomyosarcoma,C1515893,,,MONDO:0004013,adult vagina botryoid embryonal rhabdomyosarcoma,
+BMGC_DS09453,BMG_DS035379,,,,,,,DOID:7632,Cowper gland carcinoma,C1516284,,,MONDO:0004311,carcinoma of Cowper glands,
+BMGC_DS09454,BMG_DS035380,,,,,,,DOID:6721,Littre gland carcinoma,C1516285,,,MONDO:0003975,Littre gland carcinoma,
+BMGC_DS09455,BMG_DS035381,,,,,,,DOID:5152,cellular neurofibroma,C1516371,,,MONDO:0003305,cellular neurofibroma,
+BMGC_DS09456,BMG_DS035383,,,,,,,DOID:6428,cervical adenoid basal carcinoma,C1516403,,,MONDO:0006132,cervical adenoid basal carcinoma,
+BMGC_DS09457,BMG_DS035384,,,,,,,DOID:4995,cervical adenomyoma,C1516404,,,MONDO:0003238,cervical adenomyoma,
+BMGC_DS09458,BMG_DS035385,,,,,,,DOID:8177,endocervical type cervical adenomyoma,C1516405,,,MONDO:0004486,endocervical type cervical adenomyoma,
+BMGC_DS09459,BMG_DS035386,,,,,,,DOID:8361,glassy cell variant cervical adenosquamous carcinoma,C1516407,,,MONDO:0004542,"cervical adenosquamous carcinoma, glassy cell variant",
+BMGC_DS09460,BMG_DS035387,,,,,,,DOID:4442,cervical alveolar soft part sarcoma,C1516408,,,MONDO:0003003,cervical alveolar soft part sarcoma,
+BMGC_DS09461,BMG_DS035388,,,,,,,DOID:8179,cervical atypical polypoid adenomyoma,C1516409,,,MONDO:0004488,cervical atypical polypoid adenomyoma,
+BMGC_DS09462,BMG_DS035390,,,,,,,DOID:6659,cervical large cell neuroendocrine carcinoma,C1516417,,,MONDO:0006138,cervical large cell neuroendocrine carcinoma,
+BMGC_DS09463,BMG_DS035391,,,,,,,DOID:7598,cervical lymphoepithelioma-like carcinoma,C1516418,,,MONDO:0004296,cervical lymphoepithelioma-like carcinoma,
+BMGC_DS09464,BMG_DS035392,,,,,,,DOID:5368,Wolffian duct adenocarcinoma,C1516419,,,MONDO:0003410,Wolffian duct adenocarcinoma,
+BMGC_DS09465,BMG_DS035393,,,,,,,DOID:4112,cervical carcinosarcoma,C1516420,,,,,
+BMGC_DS09466,BMG_DS035394,,,,,,,DOID:8339,intestinal variant cervical mucinous adenocarcinoma,C1516422,,,MONDO:0004537,intestinal variant cervical mucinous adenocarcinoma,
+BMGC_DS09467,BMG_DS035395,,,,,,,DOID:6627,cervical adenoma malignum,C1516423,,,MONDO:0006140,"cervical mucinous adenocarcinoma, minimal deviation variant",
+BMGC_DS09468,BMG_DS035396,,,,,,,DOID:6101,signet ring cell variant cervical mucinous adenocarcinoma,C1516424,,,MONDO:0003768,signet ring cell variant cervical mucinous adenocarcinoma,
+BMGC_DS09469,BMG_DS035397,,,,,,,DOID:4111,cervical adenosarcoma,C1516426,,,MONDO:0002876,cervical adenosarcoma,
+BMGC_DS09470,BMG_DS035399,,,,,,,DOID:5752,cervical serous adenocarcinoma,C1516431,,,MONDO:0003631,cervical serous adenocarcinoma,
+BMGC_DS09471,BMG_DS035400,,,,,,,DOID:3743,cervical verrucous carcinoma,C1516435,,,MONDO:0002761,cervical verrucous carcinoma,
+BMGC_DS09472,BMG_DS035401,,,,,,,DOID:5190,cervical Wilms' tumor,C1516437,,,MONDO:0006144,cervical Wilms tumor,
+BMGC_DS09473,BMG_DS035402,,,,,,,DOID:8083,classic congenital mesoblastic nephroma,C1516475,,,MONDO:0004455,classic congenital mesoblastic nephroma,
+BMGC_DS09474,BMG_DS035403,,,,,,,DOID:7642,cholangiolocellular carcinoma,C1516490,,,MONDO:0004315,cholangiolocellular carcinoma,
+BMGC_DS09475,BMG_DS035404,,,,,,,DOID:8106,cellular phase chronic idiopathic myelofibrosis,C1516553,,,MONDO:0004463,cellular phase chronic idiopathic myelofibrosis,
+BMGC_DS09476,BMG_DS035405,,,,,,,DOID:4293,clear cell basal cell carcinoma,C1516599,,,MONDO:0002950,skin clear cell basal cell carcinoma,
+BMGC_DS09477,BMG_DS035406,,,,,,,DOID:7951,Schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma,C1516760,,,MONDO:0004408,schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma,
+BMGC_DS09478,BMG_DS035407,,,,,,,DOID:7949,stroma-dominant and stroma-poor composite ganglioneuroblastoma,C1516761,,,MONDO:0004407,stroma-dominant and stroma-poor composite ganglioneuroblastoma,
+BMGC_DS09479,BMG_DS035409,,,,,,,DOID:7139,endometrial small cell carcinoma,C1516858,,,MONDO:0006197,endometrial small cell carcinoma,
+BMGC_DS09480,BMG_DS035410,,,,,,,DOID:4005,endometrial transitional cell carcinoma,C1516864,,,MONDO:0002832,endometrial transitional cell carcinoma,
+BMGC_DS09481,BMG_DS035412,,,,,,,DOID:5478,fallopian tube adenofibroma,C1517109,,,MONDO:0003461,fallopian tube serous adenofibroma,
+BMGC_DS09482,BMG_DS035414,,,,,,,DOID:8211,fallopian tube cystadenofibroma,C1517111,,,MONDO:0004501,fallopian tube cystadenofibroma,
+BMGC_DS09483,BMG_DS035415,,,,,,,DOID:5831,fallopian tube endometrioid adenocarcinoma,C1517113,,,MONDO:0021576,fallopian tube endometrioid tumor,
+BMGC_DS09484,BMG_DS035416,,,,,,,DOID:5324,fallopian tube germ cell cancer,C1517114,,,MONDO:0003392,fallopian tube germ cell tumor,
+BMGC_DS09485,BMG_DS035418,,,,,,,DOID:1965,fallopian tube leiomyosarcoma,C1517116,,,MONDO:0002159,fallopian tube leiomyosarcoma,
+BMGC_DS09486,BMG_DS035419,,,,,,,DOID:1970,fallopian tube carcinosarcoma,C1517117,,,MONDO:0006207,fallopian tube carcinosarcoma,
+BMGC_DS09487,BMG_DS035420,,,,,,,DOID:3704,fallopian tube mucinous adenocarcinoma,C1517119,,,MONDO:0002744,fallopian tube mucinous adenocarcinoma,
+BMGC_DS09488,BMG_DS035422,,,,,,,DOID:1973,fallopian tube adenosarcoma,C1517121,,,MONDO:0002162,fallopian tube adenosarcoma,
+BMGC_DS09489,BMG_DS035424,,,,,,,DOID:5598,fallopian tube serous adenocarcinoma,C1517124,,,MONDO:0006208,fallopian tube serous adenocarcinoma,
+BMGC_DS09490,BMG_DS035425,,,,,,,DOID:5564,fallopian tube teratoma,C1517127,,,MONDO:0003515,fallopian tube teratoma,
+BMGC_DS09491,BMG_DS035426,,,,,,,DOID:4008,fallopian tube transitional cell carcinoma,C1517128,,,MONDO:0002833,fallopian tube transitional cell carcinoma,
+BMGC_DS09492,BMG_DS035427,,,,,,,DOID:738,female urethral cancer,C1517154,,,MONDO:0004203,female urethral cancer,
+BMGC_DS09493,BMG_DS035428,,,,,,,DOID:5194,intermixed schwannian stroma-rich ganglioneuroblastoma,C1517444,,,MONDO:0003326,intermixed schwannian stroma-rich ganglioneuroblastoma,
+BMGC_DS09494,BMG_DS035429,,,,,,,DOID:5193,nodular ganglioneuroblastoma,C1517445,,,MONDO:0003325,nodular ganglioneuroblastoma,
+BMGC_DS09495,BMG_DS035430,,,,,,,DOID:7591,gestational ovarian choriocarcinoma,C1517538,,,MONDO:0004294,gestational ovarian choriocarcinoma,
+BMGC_DS09496,BMG_DS035431,,,,,,,DOID:6976,micropapillary variant infiltrating bladder urothelial carcinoma,C1517579,,,MONDO:0004057,micropapillary variant infiltrating bladder urothelial carcinoma,
+BMGC_DS09497,BMG_DS035432,,,,,,,DOID:7483,cervical keratinizing squamous cell carcinoma,C1517658,,,MONDO:0004239,cervical keratinizing squamous cell carcinoma,
+BMGC_DS09498,BMG_DS035433,,,,,,,DOID:10567,late yaws,C1517744,,,MONDO:0001066,late yaws,
+BMGC_DS09499,BMG_DS035435,,,,,,,DOID:7076,breast lipid-rich carcinoma,C1517894,,,MONDO:0021090,lipid-rich breast carcinoma,
+BMGC_DS09500,BMG_DS035437,,,,,,,DOID:736,male urethral cancer,C1518164,,,MONDO:0004197,male urethral cancer,
+BMGC_DS09501,BMG_DS035438,,,,,,,DOID:6776,breast myoepithelial carcinoma,C1518167,,,MONDO:0003990,malignant breast myoepithelioma,
+BMGC_DS09502,BMG_DS035439,,,,,,,DOID:4112,cervical carcinosarcoma,C1518168,,,,,
+BMGC_DS09503,BMG_DS035441,,,,,,,DOID:6212,ovarian endometrial cancer,C1518231,,,MONDO:0003812,ovarian endometrial cancer,
+BMGC_DS09504,BMG_DS035442,,,,,,,DOID:6067,ovarian mucinous neoplasm,C1518233,,,MONDO:0024282,mucinous ovarian cancer,
+BMGC_DS09505,BMG_DS035443,,,,,,,DOID:5744,ovary serous adenocarcinoma,C1518234,,,MONDO:0024885,malignant ovarian serous tumor,
+BMGC_DS09506,BMG_DS035444,,,,,,,DOID:2151,malignant ovarian surface epithelial-stromal neoplasm,C1518236,,,,,
+BMGC_DS09507,BMG_DS035445,,,,,,,DOID:7665,non-gestational ovarian choriocarcinoma,C1518355,,,MONDO:0004322,non-gestational ovarian choriocarcinoma,
+BMGC_DS09508,BMG_DS035446,,,,,,,DOID:6239,non-invasive bladder papillary urothelial neoplasm,C1518358,,,MONDO:0003822,non-invasive bladder papillary urothelial neoplasm,
+BMGC_DS09509,BMG_DS035447,,,,,,,DOID:6065,urinary tract non-invasive transitional cell neoplasm,C1518361,,,MONDO:0003755,urinary tract non-invasive transitional cell neoplasm,
+BMGC_DS09510,BMG_DS035448,,,,,,,DOID:7961,cervical non-keratinizing squamous cell carcinoma,C1518366,,,MONDO:0004413,cervical non-keratinizing squamous cell carcinoma,
+BMGC_DS09511,BMG_DS035449,,,,,,,DOID:6585,breast oncocytic carcinoma,C1518574,,,MONDO:0003935,oncocytic breast carcinoma,
+BMGC_DS09512,BMG_DS035450,,,,,,,DOID:6232,ovarian biphasic or triphasic teratoma,C1518691,,,MONDO:0003821,ovarian biphasic or triphasic teratoma,
+BMGC_DS09513,BMG_DS035451,,,,,,,DOID:5304,ovarian clear cell adenocarcinoma,C1518693,,,MONDO:0006045,ovarian clear cell adenocarcinoma,
+BMGC_DS09514,BMG_DS035452,,,,,,,DOID:5897,ovarian clear cell adenofibroma,C1518694,,,MONDO:0003695,ovarian clear cell adenofibroma,
+BMGC_DS09515,BMG_DS035453,,,,,,,DOID:5896,ovarian clear cell cystadenofibroma,C1518695,,,MONDO:0003694,ovarian clear cell cystadenofibroma,
+BMGC_DS09516,BMG_DS035454,,,,,,,DOID:6445,ovarian endometrioid malignant adenofibroma,C1518711,,,MONDO:0003879,ovarian endometrioid adenocarcinofibroma,
+BMGC_DS09517,BMG_DS035455,,,,,,,DOID:7191,ovarian endometrioid cystadenoma,C1518713,,,MONDO:0004136,ovarian endometrioid cystadenoma,
+BMGC_DS09518,BMG_DS035456,,,,,,,DOID:6314,ovarian fetiform teratoma,C1518715,,,MONDO:0003851,ovarian fetiform teratoma,
+BMGC_DS09519,BMG_DS035457,,,,,,,DOID:3578,ovarian gonadoblastoma,C1518716,,424500,MONDO:0002697,ovarian gonadoblastoma,
+BMGC_DS09520,BMG_DS035458,,,,,,,DOID:2150,ovarian lymphoma,C1518720,,,MONDO:0002227,ovarian lymphoma,
+BMGC_DS09521,BMG_DS035459,,,,,,,DOID:2143,ovarian malignant mesothelioma,C1518721,,,MONDO:0002223,ovarian malignant mesothelioma,
+BMGC_DS09522,BMG_DS035460,,,,,,,DOID:6469,ovarian mucinous adenofibroma,C1518723,,,MONDO:0003887,ovarian mucinous adenofibroma,
+BMGC_DS09523,BMG_DS035461,,,,,,,DOID:7013,ovarian mucinous cystadenofibroma,C1518725,,,MONDO:0004074,ovarian mucinous cystadenofibroma,
+BMGC_DS09524,BMG_DS035462,,,,,,,DOID:5351,ovarian primitive germ cell tumor,C1518727,,,MONDO:0003408,ovarian primitive germ cell tumor,
+BMGC_DS09525,BMG_DS035463,,,,,,,DOID:5474,ovarian serous adenofibroma,C1518729,,,MONDO:0006340,ovarian serous adenofibroma,
+BMGC_DS09526,BMG_DS035467,,,,,,,DOID:7347,ovarian stromal hyperthecosis,C1518743,,,MONDO:0004194,ovarian stromal hyperthecosis,
+BMGC_DS09527,BMG_DS035468,,,,,,,DOID:2153,ovarian Wilms' cancer,C1518746,,,MONDO:0002230,ovarian Wilms tumor,
+BMGC_DS09528,BMG_DS035469,,,,,,,DOID:6511,glandular pattern ovarian yolk sac tumor,C1518747,,,MONDO:0003905,"ovarian yolk sac tumor, glandular pattern",
+BMGC_DS09529,BMG_DS035470,,,,,,,DOID:6512,hepatoid pattern ovarian yolk sac tumor,C1518748,,,MONDO:0003906,"ovarian yolk sac tumor, hepatoid pattern",
+BMGC_DS09530,BMG_DS035471,,,,,,,DOID:6514,polyvesicular vitelline pattern ovarian yolk sac tumor,C1518749,,,MONDO:0003907,"ovarian yolk sac tumor, polyvesicular vitelline pattern",
+BMGC_DS09531,BMG_DS035472,,,,,,,DOID:6865,oxyphilic endometrial endometrioid adenocarcinoma,C1518768,,,MONDO:0004019,oxyphilic endometrial endometrioid adenocarcinoma,
+BMGC_DS09532,BMG_DS035474,,,,,,,DOID:7236,pancreatic invasive mucinous cystadenocarcinoma,C1518870,,,MONDO:0004158,pancreatic mucinous-cystic neoplasm with an associated invasive carcinoma,
+BMGC_DS09533,BMG_DS035475,,,,,,,DOID:8150,pancreatic invasive intraductal papillary-mucinous carcinoma,C1518871,,,MONDO:0004481,pancreatic intraductal papillary-mucinous neoplasm with an associated invasive carcinoma,
+BMGC_DS09534,BMG_DS035476,,,,,,,DOID:7235,pancreatic mucinous cystadenoma,C1518872,,,MONDO:0044879,pancreatic mucinous-cystic neoplasm,
+BMGC_DS09535,BMG_DS035477,,,,,,,DOID:7685,pancreatic non-invasive intraductal papillary-mucinous carcinoma,C1518873,,,MONDO:0004329,pancreatic intraductal papillary-mucinous neoplasm with high grade dysplasia,
+BMGC_DS09536,BMG_DS035478,,,,,,,DOID:3919,pancreatic serous cystic neoplasm,C1518875,,,MONDO:0002810,pancreatic serous cystic neoplasm,
+BMGC_DS09537,BMG_DS035479,,,,,,,DOID:6257,chromophil adenoma of the kidney,C1518879,,,MONDO:0003829,chromophil adenoma of the kidney,
+BMGC_DS09538,BMG_DS035480,,,,,,,DOID:6975,bladder urothelial papillary carcinoma,C1518882,,,MONDO:0004056,bladder papillary urothelial carcinoma,
+BMGC_DS09539,BMG_DS035481,,,,,,,DOID:4277,penis basal cell carcinoma,C1518949,,,MONDO:0002935,penis basal cell carcinoma,
+BMGC_DS09540,BMG_DS035482,,,,,,,DOID:8223,penile urethral cancer,C1518950,,,MONDO:0004504,penile urethral cancer,
+BMGC_DS09541,BMG_DS035483,,,,,,,DOID:7520,periductal breast myoepitheliosis,C1518974,,,MONDO:0004261,periductal breast myoepitheliosis,
+BMGC_DS09542,BMG_DS035484,,,,,,,DOID:956,peripheral nerve schwannoma,C1519001,,,MONDO:0004820,peripheral nerve schwannoma,
+BMGC_DS09543,BMG_DS035485,,,,,,,DOID:4845,pilomyxoid astrocytoma,C1519086,,,MONDO:0016692,pilomyxoid astrocytoma,
+BMGC_DS09544,BMG_DS035487,,,,,,,,,C1519176,,181030,MONDO:0008401,pleomorphic adenoma,
+BMGC_DS09545,BMG_DS035488,,,,,,,DOID:4303,sarcomatoid basal cell carcinoma,C1519182,,,MONDO:0002957,sarcomatoid basal cell carcinoma,
+BMGC_DS09546,BMG_DS035489,,,,,,,DOID:8072,sarcomatous intrahepatic cholangiocarcinoma,C1519184,,,MONDO:0004451,sarcomatous intrahepatic cholangiocarcinoma,
+BMGC_DS09547,BMG_DS035490,,,,,,,DOID:5760,sebaceous breast carcinoma,C1519207,,,MONDO:0003635,sebaceous breast carcinoma,
+BMGC_DS09548,BMG_DS035491,,,,,,,DOID:14545,seminal vesicle adenocarcinoma,C1519233,,,MONDO:0001993,seminal vesicle adenocarcinoma,
+BMGC_DS09549,BMG_DS035492,,,,,,,DOID:5724,seminal vesicle cystadenoma,C1519234,,,MONDO:0003609,seminal vesicle cystadenoma,
+BMGC_DS09550,BMG_DS035493,,,,,,,DOID:4304,signet ring basal cell carcinoma,C1519320,,,MONDO:0002958,signet ring basal cell carcinoma,
+BMGC_DS09551,BMG_DS035494,,,,,,,DOID:7733,signet ring cell intrahepatic cholangiocarcinoma,C1519321,,,MONDO:0004346,signet ring cell intrahepatic cholangiocarcinoma,
+BMGC_DS09552,BMG_DS035496,,,,,,,DOID:7459,acantholytic variant squamous cell breast carcinoma,C1519485,,,MONDO:0004229,acantholytic variant squamous cell breast carcinoma,
+BMGC_DS09553,BMG_DS035497,,,,,,,DOID:7461,large cell keratinizing variant squamous cell breast carcinoma,C1519486,,,MONDO:0004232,large cell keratinizing variant squamous cell breast carcinoma,
+BMGC_DS09554,BMG_DS035498,,,,,,,DOID:7460,spindle cell variant squamous cell breast carcinoma,C1519487,,,MONDO:0004231,spindle cell variant squamous cell breast carcinoma,
+BMGC_DS09555,BMG_DS035500,,,,,,,DOID:6258,type 1 papillary adenoma of the kidney,C1519706,,,MONDO:0003830,type 1 papillary adenoma of the kidney,
+BMGC_DS09556,BMG_DS035501,,,,,,,DOID:6259,type 2 papillary adenoma of the kidney,C1519710,,,MONDO:0003831,type 2 papillary adenoma of the kidney,
+BMGC_DS09557,BMG_DS035503,,,,,,,DOID:6936,ureter urothelial papilloma,C1519823,,,MONDO:0004044,ureter urothelial papilloma,
+BMGC_DS09558,BMG_DS035504,,,,,,,DOID:2140,urethral urothelial papilloma,C1519826,,,MONDO:0002221,urethral urothelial papilloma,
+BMGC_DS09559,BMG_DS035505,,,,,,,DOID:3749,urethral verrucous carcinoma,C1519827,,,MONDO:0002763,urethral verrucous carcinoma,
+BMGC_DS09560,BMG_DS035506,,,,,,,DOID:5643,urethral villous adenoma,C1519828,,,MONDO:0003565,urethral villous adenoma,
+BMGC_DS09561,BMG_DS035508,,,,,,,DOID:7878,uterine corpus atypical polypoid adenomyoma,C1519844,,,MONDO:0004386,uterine corpus atypical polypoid adenomyoma,
+BMGC_DS09562,BMG_DS035509,,,,,,,DOID:7242,uterine corpus cellular leiomyoma,C1519845,,,MONDO:0004162,uterine corpus cellular leiomyoma,
+BMGC_DS09563,BMG_DS035510,,,,,,,DOID:13953,uterine corpus dissecting leiomyoma,C1519847,,,MONDO:0001842,uterine corpus dissecting leiomyoma,
+BMGC_DS09564,BMG_DS035511,,,,,,,DOID:4227,uterine corpus endometrial stromal sarcoma,C1519849,,,MONDO:0002923,uterine corpus endometrial stromal sarcoma,
+BMGC_DS09565,BMG_DS035512,,,,,,,DOID:13951,uterine corpus epithelioid leiomyoma,C1519850,,,MONDO:0001841,uterine corpus epithelioid leiomyoma,
+BMGC_DS09566,BMG_DS035513,,,,,,,DOID:6139,uterine corpus epithelioid leiomyosarcoma,C1519851,,,MONDO:0003782,uterine corpus epithelioid leiomyosarcoma,
+BMGC_DS09567,BMG_DS035514,,,,,,,DOID:7241,uterine corpus apoplectic leiomyoma,C1519852,,,MONDO:0004161,uterine corpus apoplectic leiomyoma,
+BMGC_DS09568,BMG_DS035517,,,,,,,DOID:13957,uterine corpus lipoleiomyoma,C1519856,,,MONDO:0001845,uterine corpus lipoleiomyoma,
+BMGC_DS09569,BMG_DS035519,,,,,,,DOID:3707,endometrial mucinous adenocarcinoma,C1519859,,,MONDO:0002747,endometrial mucinous adenocarcinoma,
+BMGC_DS09570,BMG_DS035520,,,,,,,DOID:13956,uterine corpus myxoid leiomyoma,C1519860,,,MONDO:0001844,uterine corpus myxoid leiomyoma,
+BMGC_DS09571,BMG_DS035521,,,,,,,DOID:6567,uterine corpus myxoid leiomyosarcoma,C1519861,,,MONDO:0003928,uterine corpus myxoid leiomyosarcoma,
+BMGC_DS09572,BMG_DS035522,,,,,,,DOID:7437,uterus perivascular epithelioid cell tumor,C1519862,,,MONDO:0004221,uterine corpus perivascular epithelioid cell tumor,
+BMGC_DS09573,BMG_DS035524,,,,,,,DOID:5727,uterine ligament cancer,C1519870,,,MONDO:0021629,uterine ligament neoplasm,
+BMGC_DS09574,BMG_DS035525,,,,,,,DOID:5747,uterine ligament serous adenocarcinoma,C1519872,,,MONDO:0003626,uterine ligament serous adenocarcinoma,
+BMGC_DS09575,BMG_DS035527,,,,,,,DOID:5402,vaginal adenoma,C1519913,,,MONDO:0003434,vaginal adenoma,
+BMGC_DS09576,BMG_DS035528,,,,,,,DOID:4117,vaginal adenosarcoma,C1519914,,,MONDO:0002881,vaginal adenosarcoma,
+BMGC_DS09577,BMG_DS035529,,,,,,,DOID:136,vaginal carcinosarcoma,C1519918,,,MONDO:0006488,vaginal carcinosarcoma,
+BMGC_DS09578,BMG_DS035530,,,,,,,DOID:134,vaginal glandular tumor,C1519921,,,MONDO:0001704,vaginal glandular neoplasm,
+BMGC_DS09579,BMG_DS035531,,,,,,,DOID:136,vaginal carcinosarcoma,C1519924,,,,,
+BMGC_DS09580,BMG_DS035533,,,,,,,DOID:138,vaginal squamous tumor,C1519931,,,MONDO:0001806,vaginal squamous tumor,
+BMGC_DS09581,BMG_DS035534,,,,,,,DOID:8104,vaginal tubulovillous adenoma,C1519933,,,MONDO:0004461,vaginal tubulovillous adenoma,
+BMGC_DS09582,BMG_DS035535,,,,,,,DOID:6613,vaginal villous adenoma,C1519936,,,MONDO:0003946,vaginal villous adenoma,
+BMGC_DS09583,BMG_DS035536,,,,,,,DOID:6569,micropapillomatosis labialis,C1519982,,,MONDO:0003929,vestibular micropapillomatosis,
+BMGC_DS09584,BMG_DS035537,,,,,,,DOID:5313,vulvar alveolar soft part sarcoma,C1520069,,,MONDO:0003391,vulvar alveolar soft part sarcoma,
+BMGC_DS09585,BMG_DS035538,,,,,,,DOID:7567,vulvar clear cell hidradenocarcinoma,C1520076,,,MONDO:0004283,vulvar clear cell hidradenocarcinoma,
+BMGC_DS09586,BMG_DS035539,,,,,,,DOID:7565,vulvar eccrine porocarcinoma,C1520081,,,MONDO:0004281,vulvar eccrine porocarcinoma,
+BMGC_DS09587,BMG_DS035540,,,,,,,DOID:2076,vulvar glandular tumor,C1520082,,,MONDO:0002198,vulvar glandular neoplasm,
+BMGC_DS09588,BMG_DS035542,,,,,,,DOID:6943,vulvar inverted follicular keratosis,C1520084,,,MONDO:0006621,vulvar inverted follicular keratosis,
+BMGC_DS09589,BMG_DS035545,,,,,,,DOID:7409,vulvar non-keratinizing squamous cell carcinoma,C1520092,,,MONDO:0004213,vulvar non-keratinizing squamous cell carcinoma,
+BMGC_DS09590,BMG_DS035546,,,,,,,DOID:7491,vulvar proximal-type epithelioid sarcoma,C1520093,,,MONDO:0004243,vulvar proximal-type epithelioid sarcoma,
+BMGC_DS09591,BMG_DS035547,,,,,,,DOID:5761,vulvar sebaceous carcinoma,C1520094,,,MONDO:0003636,vulvar sebaceous carcinoma,
+BMGC_DS09592,BMG_DS035548,,,,,,,DOID:2072,vulvar squamous tumor,C1520097,,,MONDO:0002195,vulvar squamous neoplasm,
+BMGC_DS09593,BMG_DS035551,,,,,,,DOID:7514,Wolffian adnexal neoplasm,C1520159,,,MONDO:0004255,Wolffian adnexal tumor,
+BMGC_DS09594,BMG_DS035552,266257000;195206000;38609002,Intermittent cerebral ischemia,,,,,,,C1521728,,,,,Temporary cerebral vascular dysfunction | Transient ischaemic attack | Transient cerebral ischemia | Transient ischemic attack | Transient cerebral ischaemia | Transient ischemic attack (disorder) | TIA - transient ischemic attack | TIA - transient ischaemic attack | Intermittent cerebral ischaemia | Intermittent cerebral ischemia | Intermittent cerebral ischemia (disorder) | Transient cerebral ischemia | Transient cerebral ischaemia | Transient cerebral ischemia (disorder)
+BMGC_DS09595,BMG_DS035555,,Bonnevie-Ullrich Syndrome,Turner Syndrome,,,,DOID:3491,Turner syndrome,C1527168,D014424,,MONDO:0100492,Bonnevie-Ullrich syndrome,
+BMGC_DS09596,BMG_DS035557,62382002,CRST syndrome,,,,,DOID:0060218,CREST syndrome,C1527226,,,,,"CRST syndrome | Calcinosis cutis, Raynaud's, sclerodactyly AND telangiectasia | CRST - Calcinosis, Raynaud's phenomenon, sclerodactyly, telangiectasia syndrome | Calcinosis, Raynaud's phenomenon, sclerodactyly, telangiectasia syndrome | Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia (CRST) syndrome | Calcinosis, Raynaud phenomenon, sclerodactyly, and telangiectasia (CRST) syndrome | Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia syndrome | Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia syndrome (disorder)"
+BMGC_DS09597,BMG_DS035558,1269423000;65389002,Adrenomyeloneuropathy,Adrenoleukodystrophy,,,E71.522,,,C1527231,D000326,,MONDO:0015339,adrenomyeloneuropathy,Adrenomyeloneuropathy (disorder) | AMN - adrenomyeloneuropathy | Adult onset adrenoleukodystrophy | Adrenomyeloneuropathy | Adrenoleukodystrophy | Bronze Schilder disease | Schilder-Addison complex | Siemerling-Creutzfeldt disease | Adrenoleukodystrophy (disorder) | X-linked adrenoleucodystrophy | Adrenoleucodystrophy | ALD - adrenoleukodystrophy | X-linked adrenoleukodystrophy
+BMGC_DS09598,BMG_DS035560,,Dental Pulp Stone,Dental Pulp Calcification,,,,,,C1527284,D003784,125420,MONDO:0007437,dentin dysplasia type II,
+BMGC_DS09599,BMG_DS035563,,Chronic Airflow Obstruction,"Pulmonary Disease, Chronic Obstructive",,,,,,C1527303,D029424,,,,
+BMGC_DS09600,BMG_DS035564,39021009,Ametropia,Refractive Errors,,,,,,C1527310,D012030,,,,Disorder of refraction | Refractive error | Disorder of refraction (disorder) | Ametropia
+BMGC_DS09601,BMG_DS035565,,,,,,,DOID:4724,brain edema,C1527311,,,,,
+BMGC_DS09602,BMG_DS035566,,Alpha-Aminoadipic Semialdehyde Deficiency Disease,Hyperlysinemias,,,,,,C1527317,D020167,,,,
+BMGC_DS09603,BMG_DS035568,,"Vertigo, Aural",Meniere Disease,,,,,,C1527320,D008575,,,,
+BMGC_DS09604,BMG_DS035569,,Pyridoxine Deficiency,Vitamin B 6 Deficiency,,,,,,C1527330,D026681,,,,
+BMGC_DS09605,BMG_DS035570,,"Transient Ischemic Attack, Anterior Circulation","Ischemic Attack, Transient",,,,,,C1527335,D002546,,,,
+BMGC_DS09606,BMG_DS035571,,Sjogren's Syndrome,Sjogren's Syndrome,,,,DOID:12894,Sjogren's syndrome,C1527336,D012859,270150,MONDO:0010030,Sjogren syndrome,
+BMGC_DS09607,BMG_DS035572,,"Familial Amyloid Polyneuropathy, Appalachian Type","Amyloid Neuropathies, Familial",,,,,,C1527337,D028227,,,,
+BMGC_DS09608,BMG_DS035573,,"Hereditary Cerebral Amyloid Angiopathy, Icelandic Type","Cerebral Amyloid Angiopathy, Familial",,,,DOID:9246,cerebral amyloid angiopathy,C1527338,D028243,105150,MONDO:0007098,ACys amyloidosis,
+BMGC_DS09609,BMG_DS035574,,,,,,,DOID:3008,invasive ductal carcinoma,C1527349,,,MONDO:0005590,breast ductal adenocarcinoma,
+BMGC_DS09610,BMG_DS035575,,Nerve Root Disorder,Radiculopathy,,,,,,C1527351,D011843,,,,
+BMGC_DS09611,BMG_DS035576,,Hepatic Form of Wilson Disease,Hepatolenticular Degeneration,,,,,,C1527352,D006527,,,,
+BMGC_DS09612,BMG_DS035577,,Algodystrophic Syndrome,Reflex Sympathetic Dystrophy,,,,,,C1527353,D012019,,,,
+BMGC_DS09613,BMG_DS035579,84326006,Phototoxicity,"Dermatitis, Phototoxic",,,,,,C1527358,D017484,,,,Phototoxicity | Phototoxicity (finding) | Photosensitisation reaction | Photosensitization reaction | Photosensitive dermatitis
+BMGC_DS09614,BMG_DS035580,,Salaam Seizures,"Spasms, Infantile",,,,DOID:0050562,West syndrome,C1527366,D013036,,,,
+BMGC_DS09615,BMG_DS035581,,Vincent Angina,"Gingivitis, Necrotizing Ulcerative",,,,DOID:13924,necrotizing ulcerative gingivitis,C1527368,D005892,,,,
+BMGC_DS09616,BMG_DS035582,,Cystic Breast Disease,Fibrocystic Breast Disease,,,,,,C1527375,D005348,,,,
+BMGC_DS09617,BMG_DS035583,156452007;201049004;90424004,Morphea,"Scleroderma, Localized",,,,,,C1527383,D012594,,,,Morphoea | Morphea | Morphoea (disorder) | Morphea | Morphoea | Morphea (disorder) | Localized scleroderma | Localised scleroderma | Localized scleroderma (disorder)
+BMGC_DS09618,BMG_DS035586,,Ogilvie Syndrome,Colonic Pseudo-Obstruction,,,,,,C1527395,D003112,,,,
+BMGC_DS09619,BMG_DS035587,,Fibrocystic Disease of Pancreas,Cystic Fibrosis,,,,,,C1527396,D003550,,,,
+BMGC_DS09620,BMG_DS035590,65323003,Rhizomelic pseudopolyarthritis,,,,,,,C1527406,,,,,Polymyalgia rheumatica | Forestier-Certonciny syndrome | Rhizomelic pseudopolyarthritis | Senile arthritis | PMR - Polymyalgia rheumatica | Polymyalgia rheumatica (disorder)
+BMGC_DS09621,BMG_DS035591,,Eosinophilic Pneumonia,Pulmonary Eosinophilia,,,,DOID:5870,eosinophilic pneumonia,C1527407,D011657,,MONDO:0005749,eosinophilic pneumonia,
+BMGC_DS09622,BMG_DS035592,16726004;197667002,Renal rickets,,GB61.Z,"Chronic kidney disease, stage unspecified",N25.0,,,C1527410,,MTHU038299,,,Renal osteodystrophy | Renal rickets | Renal bone disease | ROD - Renal osteodystrophy | Renal osteodystrophy (disorder) | Renal rickets | Renal rickets (disorder)
+BMGC_DS09623,BMG_DS035593,46085004,Thrombosis of retinal vein,,,,,,,C1527411,,,,,Thrombosis of retinal vein | Retinal vein thrombosis | Thrombosis of retinal vein (disorder)
+BMGC_DS09624,BMG_DS035594,,,,,,,DOID:7284,Skene gland carcinoma,C1527427,,,MONDO:0004173,adenocarcinoma of skene gland origin,
+BMGC_DS09625,BMG_DS035616,,,,,,,,,C1531719,,108725,MONDO:0007169,atherosclerosis susceptibility,
+BMGC_DS09626,BMG_DS035618,413936007,Currarino triad,,,,,DOID:0111546,Currarino syndrome,C1531773,C536221,176450,MONDO:0008305,Currarino triad,Currarino triad (disorder) | Currarino triad
+BMGC_DS09627,BMG_DS035650,414029004,Disorder of immune function,,,,,,,C1532237,,,,,Disorder of immune function (disorder) | Disorder of immune function | Immune system disorder
+BMGC_DS09628,BMG_DS035662,,Infectious Endophthalmitis,Endophthalmitis,,,,,,C1532322,D009877,,,,
+BMGC_DS09629,BMG_DS035708,415176004,Primary congenital glaucoma,,,,,,,C1533041,,MTHU073627,MONDO:0000365,primary congenital glaucoma,Primary congenital glaucoma (disorder) | Primary congenital glaucoma | Primary infantile glaucoma
+BMGC_DS09630,BMG_DS035720,413844008;84537008,Chronic coronary insufficiency,,,,,,,C1533195,,,,,Chronic myocardial ischemia (disorder) | Chronic myocardial ischemia | Chronic myocardial ischaemia | Chronic coronary insufficiency | Chronic ischemic heart disease | Chronic myocardial ischemia | Chronic coronary insufficiency | Chronic ischaemic heart disease | Chronic myocardial ischaemia | Chronic ischemic heart disease (disorder)
+BMGC_DS09631,BMG_DS035723,238067002,Pseudo-Zellweger syndrome,,,,,DOID:14723,beta-ketothiolase deficiency,C1533628,C535818,,,,Peroxisomal thiolase deficiency | Pseudo-Zellweger syndrome | 3-Ketoacyl-CoA thiolase deficiency | Peroxisomal thiolase deficiency (disorder)
+BMGC_DS09632,BMG_DS035730,75047002;128615009,Disorder of skeletal muscle,,,,,,,C1533847,,,MONDO:0020120,skeletal muscle disorder,Disease of skeletal muscle | Disorder of skeletal muscle | Disorder of skeletal muscle (disorder) | Disorder of skeletal muscle | Disorder of skeletal muscle (disorder)
+BMGC_DS09633,BMG_DS035732,109616007;86276007,Bleeding of subgingival space,,,,,,,C1533849,,,,,Bleeding of subgingival space | Bleeding of subgingival space (disorder) | Bleeding gums | Gingival bleeding | Gingival crevicular bleeding | Bleeding of subgingival space | Gingival crevice bleeding | Crevicular bleeding of gum | Gingival hemorrhage | Gingival haemorrhage | Bleeding gums (finding)
+BMGC_DS09634,BMG_DS036050,,,,,,,,,C1535893,,,MONDO:0001315,neurocirculatory asthenia,
+BMGC_DS09635,BMG_DS036052,,,,,,,,,C1535926,,,MONDO:0700092,neurodevelopmental disorder,
+BMGC_DS09636,BMG_DS036053,,,,,,,DOID:11339,pneumocystosis,C1535939,,,MONDO:0019121,pneumocystosis,
+BMGC_DS09637,BMG_DS036054,,Polyglandular Type III Autoimmune Syndrome,"Polyendocrinopathies, Autoimmune",,,,,,C1535942,D016884,,MONDO:0016422,autoimmune polyendocrinopathy type 3,
+BMGC_DS09638,BMG_DS036058,,Dysbacteriosis,Dysbiosis,,,,,,C1536021,D064806,,,,
+BMGC_DS09639,BMG_DS036069,231996009,Central areolar choroidal sclerosis,,,,,,,C1536451,C535358,,MONDO:0008982,central areolar choroidal dystrophy,Central areolar choroidal sclerosis | Central areolar choroidal sclerosis (disorder) | Central areolar choroidal dystrophy
+BMGC_DS09640,BMG_DS036080,124258007,Deficiency of acetyl-CoA acetyltransferase,,,,,,,C1536500,,203750,MONDO:0008760,beta-ketothiolase deficiency,Deficiency of acetoacetyl-CoA thiolase | Deficiency of acetyl-CoA acetyltransferase | Acetoacetyl-CoA thiolase deficiency | 3-Ketothiolase deficiency | alpha-Methylacetoacetic aciduria | 3-Methylhydroxybutyric acidaemia | 3-Methylhydroxybutyric acidemia | Deficiency of acetyl-coenzyme A acetyltransferase | Deficiency of acetyl-coenzyme A acetyltransferase (disorder)
+BMGC_DS09641,BMG_DS036144,13645005,"Chronic obstructive lung disease, NEC",,,,,,,C1537189,,,,,Chronic obstructive lung disease | Chronic airway obstruction | Chronic irreversible airway obstruction | Chronic airflow obstruction | CAFL - Chronic airflow limitation | COAD - Chronic obstructive airways disease | CAO - Chronic airflow obstruction | Chronic airflow limitation | CAL - Chronic airflow limitation | COPD - Chronic obstructive pulmonary disease | Chronic obstructive airway disease | Chronic airway disease | COLD - Chronic obstructive lung disease | Chronic obstructive pulmonary disease | Chronic obstructive pulmonary disease (disorder)
+BMGC_DS09642,BMG_DS036273,302917004;244815007,Pyloric obstruction,,,,,,,C1541124,,,,,Pyloric obstruction | Pyloric obstruction (disorder) | Pyloric obstruction | Gastric outflow obstruction | Pyloric obstruction (disorder)
+BMGC_DS09643,BMG_DS036363,233850007;50194006,Infective endocarditis,,,,,,,C1541923,,,MONDO:0000565,infective endocarditis,Infective endocarditis | IE - Infective endocarditis | Infective endocarditis (disorder) | Bacterial endocarditis | Bacterial endocarditis (disorder)
+BMGC_DS09644,BMG_DS036424,30575002,Pancytopenia-dysmelia syndrome,,,,,,,C1542664,,,,,Fanconi pancytopenia syndrome | Fanconi's anemia | Pancytopenia-dysmelia syndrome | Fanconi's anaemia | Fanconi's anemia (disorder) | Fanconi's hypoplastic anaemia | Fanconi's familial refractory anaemia | Fanconi's hypoplastic anemia | Fanconi's familial refractory anemia | Fanconi anemia | Fanconi anaemia
+BMGC_DS09645,BMG_DS036496,,Chronic Kidney Diseases,"Renal Insufficiency, Chronic",,,,,,C1561643,D051436,,MONDO:0005300,chronic kidney disease,
+BMGC_DS09646,BMG_DS036497,,Overweight and obesity,,,,E66,,,C1561826,,,,,
+BMGC_DS09647,BMG_DS036499,707323002,Anemia in chronic kidney disease,,,,D63.1,,,C1561828,,,,,Anemia co-occurrent and due to chronic kidney disease | Anaemia co-occurrent and due to chronic kidney disease | Anaemia in chronic kidney disease | Anemia co-occurrent and due to chronic kidney disease (disorder) | Anemia in chronic kidney disease
+BMGC_DS09648,BMG_DS036533,417183007,Fleck corneal dystrophy,,,,,DOID:0060448,Fleck corneal dystrophy,C1562113,,121850,MONDO:0007376,fleck corneal dystrophy,Fleck corneal dystrophy (disorder) | Fleck corneal dystrophy
+BMGC_DS09649,BMG_DS036559,416770009,Ocular histoplasmosis syndrome,,,,,,,C1562543,,,,,Ocular histoplasmosis syndrome (disorder) | Ocular histoplasmosis syndrome | OHS-ocular histoplasmosis syndrome
+BMGC_DS09650,BMG_DS036560,,"Leprosy, Multibacillary","Leprosy, Multibacillary",,,,,,C1562585,D056006,,MONDO:0041751,multibacillary leprosy,
+BMGC_DS09651,BMG_DS036566,417017003,Acute cerebellar syndrome,,,,,,,C1562722,,,,,Acute cerebellar syndrome (disorder) | Acute cerebellar syndrome
+BMGC_DS09652,BMG_DS036574,417006004,Twin reversal arterial perfusion syndrome,,,,,,,C1562817,,,MONDO:0041755,twin reversal arterial perfusion syndrome,Twin reversal arterial perfusion syndrome (disorder) | Twin reversal arterial perfusion syndrome | TRAP- twin reversal arterial perfusion syndrome
+BMGC_DS09653,BMG_DS036581,417065002,Thiel-Behnke corneal dystrophy,,,,,DOID:0060455,Thiel-Behnke corneal dystrophy,C1562894,C535942,602082,MONDO:0011185,Thiel-Behnke corneal dystrophy,"Thiel-Behnke corneal dystrophy (disorder) | Thiel-Behnke corneal dystrophy | CDB type II-Corneal dystrophy of Bowman's membrane, type II"
+BMGC_DS09654,BMG_DS036584,,"Leprosy, Paucibacillary","Leprosy, Paucibacillary",,,,,,C1562908,D056005,,MONDO:0041752,paucibacillary leprosy,
+BMGC_DS09655,BMG_DS036592,416597004,Dapsone resistant leprosy,,,,,,,C1563054,,,,,Dapsone resistant leprosy (disorder) | Dapsone resistant leprosy | Dapsone resistant mycobacterium leprae | Diaminodiphenylsulfone resistant leprosy | Diaminodiphenylsulphone resistant leprosy
+BMGC_DS09656,BMG_DS036624,,DNA Repair-Deficiency Disorders,DNA Repair-Deficiency Disorders,,,,,,C1563696,D049914,,,,
+BMGC_DS09657,BMG_DS036625,,Chromosome Instability Syndromes,DNA Repair-Deficiency Disorders,,,,,,C1563697,D049914,,,,
+BMGC_DS09658,BMG_DS036626,,"Nephrogenic Diabetes Insipidus, Type I","Diabetes Insipidus, Nephrogenic",,,,,,C1563705,D018500,304800,MONDO:0010581,"diabetes insipidus, nephrogenic, X-linked",
+BMGC_DS09659,BMG_DS036627,,"Nephrogenic Diabetes Insipidus, Type II","Diabetes Insipidus, Nephrogenic",,,,,,C1563706,D018500,125800,MONDO:0007451,"diabetes insipidus, nephrogenic, autosomal",
+BMGC_DS09660,BMG_DS036628,,Myopathic Ophthalmopathy,Graves Ophthalmopathy,,,,DOID:0081120,Graves ophthalmopathy,C1563709,D049970,,,,
+BMGC_DS09661,BMG_DS036629,,Andersen Syndrome,Andersen Syndrome,,,,DOID:0050434,Andersen-Tawil syndrome,C1563715,D050030,170390,MONDO:0008222,Andersen-Tawil syndrome,
+BMGC_DS09662,BMG_DS036630,,Genital Infantilism,Sexual Infantilism,,,,,,C1563718,D050035,,,,
+BMGC_DS09663,BMG_DS036631,,Kallmann Syndrome 1,Kallmann Syndrome,,,,,,C1563719,D017436,308700,MONDO:0010635,hypogonadotropic hypogonadism 1 with or without anosmia,
+BMGC_DS09664,BMG_DS036632,,Kallmann Syndrome 2,Kallmann Syndrome,,,,,,C1563720,D017436,147950,MONDO:0007844,hypogonadotropic hypogonadism 2 with or without anosmia,
+BMGC_DS09665,BMG_DS036635,,"Headache Disorders, Primary","Headache Disorders, Primary",,,,,,C1565106,D051270,,,,
+BMGC_DS09666,BMG_DS036639,,Cholera Infantum,Gastrointestinal Diseases,,,,,,C1565321,D005767,,,,
+BMGC_DS09667,BMG_DS036640,,Renal Insufficiency,Renal Insufficiency,,,,,,C1565489,D051437,,,,
+BMGC_DS09668,BMG_DS036641,,Acute Kidney Insufficiency,Acute Kidney Injury,,,,DOID:3021,acute kidney failure,C1565662,D058186,,,,
+BMGC_DS09669,BMG_DS036642,,"Direct Hyperbilirubinemia, Neonatal","Hyperbilirubinemia, Neonatal",,,,,,C1565885,D051556,,,,
+BMGC_DS09670,BMG_DS036643,,"Indirect Hyperbilirubinemia, Neonatal","Hyperbilirubinemia, Neonatal",,,,,,C1565886,D051556,,,,
+BMGC_DS09671,BMG_DS036645,,,,,,,DOID:4211,posterior fossa meningioma,C1565950,,,MONDO:0002919,posterior cranial fossa meningioma,
+BMGC_DS09672,BMG_DS036646,,Icterus Gravis Neonatorum,"Jaundice, Neonatal",,,,,,C1566050,D007567,,MONDO:0006584,obsolete neonatal jaundice,
+BMGC_DS09673,BMG_DS036647,,Preterm Premature Rupture of Fetal Membranes,"Fetal Membranes, Premature Rupture",,,,,,C1566302,D005322,,,,
+BMGC_DS09674,BMG_DS036648,,Unilateral Multicystic Dysplastic Kidney,Multicystic Dysplastic Kidney,,,,,,C1567426,D021782,,MONDO:0019981,unilateral multicystic dysplastic kidney,
+BMGC_DS09675,BMG_DS036649,,Alport Syndrome,"Nephritis, Hereditary",,,,,,C1567741,D009394,,MONDO:0018965,Alport syndrome,
+BMGC_DS09676,BMG_DS036650,,"Alport Syndrome, X-Linked","Nephritis, Hereditary",,,,,,C1567742,D009394,,,,
+BMGC_DS09677,BMG_DS036651,,"Alport Syndrome, Autosomal Dominant","Nephritis, Hereditary",,,,,,C1567743,D009394,,,,
+BMGC_DS09678,BMG_DS036652,,"Alport Syndrome, Autosomal Recessive","Nephritis, Hereditary",,,,,,C1567744,D009394,,,,
+BMGC_DS09679,BMG_DS036653,,,,,,,,,C1568247,,,MONDO:0010168,Usher syndrome type 1,
+BMGC_DS09680,BMG_DS036654,,"Usher Syndrome, Type III",Usher Syndromes,,,,DOID:0110829;DOID:0110827;DOID:0110828,Usher syndrome type 2 | retinitis pigmentosa-deafness syndrome | Usher syndrome type 3,C1568248,D052245,,MONDO:0016485,Usher syndrome type 3,
+BMGC_DS09681,BMG_DS036655,,"Usher Syndrome, Type II",Usher Syndromes,,,,DOID:0110827;DOID:0110828,Usher syndrome type 2 | Usher syndrome type 3,C1568249,D052245,611383,MONDO:0012662,Usher syndrome type 2D,
+BMGC_DS09682,BMG_DS036656,,Tendinopathy,Tendinopathy,,,,,,C1568272,D052256,,,,
+BMGC_DS09683,BMG_DS036657,724152009;430671000124105,Tendinosis,Tendinopathy,,,,,,C1568363,D052256,,MONDO:0100011,tendinosis,Tendinosis (disorder) | Tendinosis | Tendinosis (finding) | Tendinosis
+BMGC_DS09684,BMG_DS036658,,Oral Mucositis,Stomatitis,,,,,,C1568868,D013280,,,,
+BMGC_DS09685,BMG_DS036762,197673001;1776003,Renotubular acidemia,,,,,,,C1578594,,,,,(Acidemia: [renal] or [renotubular]) or other impaired renal function disorder NOS | Other impaired renal function disorder NOS | Renal acidemia | Renotubular acidemia | (Acidaemia: [renal] or [renotubular]) or other impaired renal function disorder NOS | Renotubular acidaemia | Renal acidaemia | (Acidaemia: [renal] or [renotubular]) or other impaired renal function disorder NOS (disorder) | Renal tubular acidosis | Renal tubular acidosis (disorder) | RTA - Renal tubular acidosis | Renotubular acidaemia | Renotubular acidemia
+BMGC_DS09686,BMG_DS036782,266655004;155981006,(Vaginitis &/or vulvovaginitis (& non specified)) or (bacterial vaginosis) or (vulvitis non specified),,,,,,,C1578688,,,,,Vulvitis - non sp. | Vulvovaginitis | Vaginitis - non sp. | Vaginitis/vulvovaginitis | Vulvo-vaginitis | Bacterial vaginosis | (Vaginitis &/or vulvovaginitis (& non specified)) or (bacterial vaginosis) or (vulvitis non specified) | (Vaginitis &/or vulvovaginitis (& non specified)) or (bacterial vaginosis) or (vulvitis non specified) (disorder) | Bacterial vaginosis | Vaginitis - non sp. | Vulvitis - non sp. | Vulvovaginitis | Vaginitis/vulvovaginitis | Vulvo-vaginitis | (Vaginitis &/or vulvovaginitis (& non specified)) or (bacterial vaginosis) or (vulvitis non specified) | (Vaginitis &/or vulvovaginitis (& non specified)) or (bacterial vaginosis) or (vulvitis non specified) (disorder)
+BMGC_DS09687,BMG_DS036785,,"Myxedema, Congenital",Congenital Hypothyroidism,,,,,,C1578691,D003409,,,,
+BMGC_DS09688,BMG_DS036825,,,,,,,,,C1578917,,147630,MONDO:0007834,islet cell adenomatosis,
+BMGC_DS09689,BMG_DS036844,35533001;155856009;197654000;90688005,Chronic uremia,,,,,,,C1579029,,,,,"Chronic uremia | Chronic uraemia | Chronic uremia (disorder) | Renal failure: [chronic] or [end stage] | End stage renal failure | Renal failure - chronic | Renal failure (chronic) | Chronic renal failure | Failure, renal -chronic | Chronic uremia | Uremia - chronic | Chronic uraemia | Uraemia - chronic | Renal failure: [chronic] or [end stage] (disorder) | Chronic uremia | Uremia - chronic | Chronic uraemia | Uraemia - chronic | Renal failure: [chronic] or [end stage] | Failure, renal -chronic | Renal failure (chronic) | Chronic renal failure | Renal failure - chronic | End stage renal failure | Renal failure: [chronic] or [end stage] (disorder) | Chronic renal failure syndrome | Chronic uraemia | Chronic uremia | CRF - Chronic renal failure | Chronic renal failure | Chronic renal failure syndrome (disorder)"
+BMGC_DS09690,BMG_DS036923,,Megacystis microcolon intestinal hypoperistalsis syndrome,,,,,DOID:0060610,megacystis-microcolon-intestinal hypoperistalsis syndrome,C1608393,C536138,,MONDO:0025986,megacystis-microcolon-intestinal hypoperistalsis syndrome,
+BMGC_DS09691,BMG_DS036927,,Mycobacterium abscessus Infection,"Mycobacterium Infections, Nontuberculous",,,,,,C1608955,D009165,,,,
+BMGC_DS09692,BMG_DS036929,41962002,Congenital absence of kidneys syndrome,,,,,,,C1609433,,,MONDO:0015986,bilateral renal agenesis,Oligohydramnios sequence | Potter syndrome | Renofacial syndrome | Renal agenesis syndrome | Congenital absence of kidneys syndrome | Oligohydramnios sequence (disorder) | BRA - Bilateral renal agenesis | Potter's anomaly of the kidney | Bilateral congenital absence of kidneys
+BMGC_DS09693,BMG_DS036931,,Latent Tuberculosis,Latent Tuberculosis,,,,,,C1609538,D055985,,MONDO:0040753,latent tuberculosis infection,
+BMGC_DS09694,BMG_DS036943,,Nephrogenic Fibrosing Dermopathy,Nephrogenic Fibrosing Dermopathy,,,,,,C1619692,D054989,,,,
+BMGC_DS09695,BMG_DS036944,,,,,,,,,C1619700,,191830,MONDO:0024519,renal hypodysplasia/aplasia 1,
+BMGC_DS09696,BMG_DS036945,716203000,Decompensated cirrhosis of liver,,,,,,,C1619727,,,,,Decompensated cirrhosis of liver (disorder) | Decompensated cirrhosis of liver | Decompensated cirrhosis
+BMGC_DS09697,BMG_DS036946,,Gout flare,,,,M10,,,C1619733,,,,,
+BMGC_DS09698,BMG_DS036953,69886008;155356003;195039008,Partial atrioventricular block,,,,,,,C1621824,,,,,Incomplete atrioventricular block | Partial atrioventricular block | Incomplete heart block | Second degree heart block | Partial heart block | Incomplete atrioventricular block (disorder) | Partial atrioventricular block | Partial atrioventricular block (disorder) | Partial atrioventricular block | Partial atrioventricular block (disorder) | Incomplete atrioventricular block | Incomplete heart block | Partial heart block
+BMGC_DS09699,BMG_DS036955,419920004,Adrenal hyperplasia,,,,,,,C1621895,,MTHU014670,,,Adrenal hyperplasia (disorder) | Adrenal hyperplasia
+BMGC_DS09700,BMG_DS036956,,Intermediate Maple Syrup Urine Disease,Maple Syrup Urine Disease,,,,,,C1621920,D008375,,MONDO:0017052,intermediate maple syrup urine disease,
+BMGC_DS09701,BMG_DS036957,419398009,Meretoja syndrome,,,,,,,C1622345,C537459,105120,MONDO:0007097,Finnish type amyloidosis,Meretoja syndrome (disorder) | Meretoja syndrome | Amyloid cranial neuropathy with lattice corneal dystrophy | Meretoja type amyloidosis
+BMGC_DS09702,BMG_DS036959,,"Corneal Dystrophy, Central Type",,,,,,,C1622427,C563262,217600,MONDO:0009018,central cloudy dystrophy of François,
+BMGC_DS09703,BMG_DS036963,,Cirrhosis,Fibrosis,,,,,,C1623038,D005355,,,,
+BMGC_DS09704,BMG_DS036964,,Okihiro Syndrome,Duane Retraction Syndrome,,,,,,C1623209,D004370,607323,MONDO:0011812,Duane-radial ray syndrome,
+BMGC_DS09705,BMG_DS036995,,"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY",,,,,,,C1631597,,604772;600996;604772,MONDO:0011484,catecholaminergic polymorphic ventricular tachycardia 1,
+BMGC_DS09706,BMG_DS036996,418171008,Complicated appendicitis,,,,,,,C1632842,,,,,Complicated appendicitis (disorder) | Complicated appendicitis
+BMGC_DS09707,BMG_DS037005,,"Macular dystrophy, corneal type 1",,,,,,,C1636149,C537834,217800,MONDO:0009020,macular corneal dystrophy,
+BMGC_DS09708,BMG_DS037026,419039007,Groenouw corneal dystrophy type I (disorder),,,,,,,C1641846,,121900,MONDO:0007377,granular corneal dystrophy type I,Groenouw corneal dystrophy type I | Granular corneal dystrophy type I | Granular corneal dystrophy type I (disorder)
+BMGC_DS09709,BMG_DS037035,,Ectopia Lentis with Ectopia of Pupil,,,,,DOID:0111648,ectopia lentis with ectopia of pupil,C1644196,C563268,225200,MONDO:0009153,ectopia lentis et pupillae,
+BMGC_DS09710,BMG_DS037038,,,,,,,,,C1656427,,,MONDO:0019939,early-onset schizophrenia,
+BMGC_DS09711,BMG_DS037057,418801006,Intraoperative floppy iris syndrome,,,,,,,C1688637,,,MONDO:0041775,intraoperative floppy iris syndrome,Intraoperative floppy iris syndrome | IFIS - intraoperative floppy iris syndrome | Intraoperative floppy iris syndrome (disorder)
+BMGC_DS09712,BMG_DS037063,419197009,Lattice corneal dystrophy Type I,,,,,,,C1690006,,122200,MONDO:0007380,lattice corneal dystrophy type I,Lattice corneal dystrophy Type I (disorder) | Lattice corneal dystrophy Type I | Biber-Haab-Dimmer dystrophy
+BMGC_DS09713,BMG_DS037073,418435001,Macular corneal dystrophy Type II (disorder),,,,,,,C1691013,,,,,Macular corneal dystrophy Type II (disorder) | Macular corneal dystrophy Type II
+BMGC_DS09714,BMG_DS037077,,Cystic Kidney Diseases,"Kidney Diseases, Cystic",,,,,,C1691228,D052177,,,,
+BMGC_DS09715,BMG_DS037084,,"Arthritis, Bacterial","Arthritis, Infectious",,,,,,C1692886,D001170,,MONDO:0004471,bacterial arthritis,
+BMGC_DS09716,BMG_DS037088,703468005,Bacterial tonsillitis,,,,,,,C1696371,,,,,Bacterial tonsillitis | Bacterial tonsillitis (disorder)
+BMGC_DS09717,BMG_DS037092,,Spontaneous hematomas,,,,,,,C1697453,,MTHU047994,,,
+BMGC_DS09718,BMG_DS037093,713886006,BK virus nephropathy,,,,,DOID:0040086,Polyomavirus-associated nephropathy,C1697878,,,MONDO:0022529,BK-virus nephropathy,Kidney disease caused by BK polyomavirus | Nephropathy caused by BK polyomavirus (disorder) | Nephropathy caused by BK polyomavirus | BK virus nephropathy
+BMGC_DS09719,BMG_DS037096,703469002,Bacterial otitis media,,,,,,,C1698510,,,,,Bacterial otitis media (disorder) | Bacterial otitis media
+BMGC_DS09720,BMG_DS037097,280221000009107,Bacterial otitis externa,,,,,,,C1699099,,,,,Bacterial otitis externa | Otitis externa caused by bacteria (disorder) | Otitis externa caused by bacteria
+BMGC_DS09721,BMG_DS037099,,"Pneumonia, Ventilator-Associated","Pneumonia, Ventilator-Associated",,,,,,C1701940,D053717,,,,
+BMGC_DS09722,BMG_DS037104,,,,,,,,,C1704231,,,MONDO:0700219,neoplastic meningitis,
+BMGC_DS09723,BMG_DS037106,,,,,,,,,C1704272,,600082,MONDO:0010811,benign prostatic hyperplasia,
+BMGC_DS09724,BMG_DS037109,65110003,Pyomyositis,Pyomyositis,,,,,,C1704275,D052880,,,,Tropical pyomyositis | Tropical myositis | Pyomyositis | Tropical pyomyositis (disorder)
+BMGC_DS09725,BMG_DS037110,,"Hypobetalipoproteinemia, Familial, Apolipoprotein B","Hypobetalipoproteinemia, Familial, Apolipoprotein B",,,,,,C1704299,D052476,,,,
+BMGC_DS09726,BMG_DS037111,773540001;9187004,Leukokeratosis,Leukoplakia,,,,,,C1704317,D007971,,,,Leukokeratosis (disorder) | Leucokeratosis | Leukokeratosis | Leukokeratosis | Keratotic plaque | Leukokeratosis (morphologic abnormality)
+BMGC_DS09727,BMG_DS037112,,"Nephrotic Syndrome, Minimal Change","Nephrosis, Lipoid",,,,,,C1704321,D009402,,,,
+BMGC_DS09728,BMG_DS037116,,Dental Diseases,Stomatognathic Diseases,,,,,,C1704330,D009057,,,,
+BMGC_DS09729,BMG_DS037117,,Hypophosphatemic Rickets,"Rickets, Hypophosphatemic",,,,,,C1704375,D063730,,MONDO:0024300,hypophosphatemic rickets,
+BMGC_DS09730,BMG_DS037119,,Bright Disease,Glomerulonephritis,,,,,,C1704377,D005921,,,,
+BMGC_DS09731,BMG_DS037120,,Heymann Nephritis,"Glomerulonephritis, Membranous",,,,,,C1704378,D015433,,,,
+BMGC_DS09732,BMG_DS037121,,Distal Renal Tubular Acidosis,"Acidosis, Renal Tubular",,,,,,C1704380,D000141,,MONDO:0015827,distal renal tubular acidosis,
+BMGC_DS09733,BMG_DS037123,,Hyperlipoproteinemia Type IIb,Hyperlipoproteinemia Type II,,,,,,C1704417,D006938,144010,MONDO:0007751,"hypercholesterolemia, autosomal dominant, type B",
+BMGC_DS09734,BMG_DS037125,,Milroy Disease,Lymphedema,,,,DOID:0070212,hereditary lymphedema I,C1704423,D008209,153100,MONDO:0007919,lymphatic malformation 1,
+BMGC_DS09735,BMG_DS037126,400040008,Hereditary lymphedema type II,,,,,DOID:0070213,hereditary lymphedema II,C1704424,,,,,Hereditary lymphedema type II (disorder) | Hereditary lymphoedema type II | Hereditary lymphedema type II | Meige lymphoedema | Meige lymphedema | Meige disease
+BMGC_DS09736,BMG_DS037128,,"Hypoalphalipoproteinemia, Familial",Hypoalphalipoproteinemias,,,,,,C1704429,D052456,,,,
+BMGC_DS09737,BMG_DS037129,,Urinary Schistosomiasis,Schistosomiasis haematobia,,,,,,C1704430,D012553,,MONDO:0006001,urinary schistosomiasis,
+BMGC_DS09738,BMG_DS037130,,Peripheral Arterial Diseases,Peripheral Arterial Disease,,,,DOID:0050830,peripheral artery disease,C1704436,D058729,,MONDO:0005386,peripheral arterial disease,
+BMGC_DS09739,BMG_DS037133,,Hyperparathyroidism-Jaw Tumor Syndrome,,,,,,,C1704981,C563273,145001,MONDO:0007768,hyperparathyroidism 2 with jaw tumors,
+BMGC_DS09740,BMG_DS037141,,"Pachyonychia Congenita, Jadassohn Lewandowsky Type",Pachyonychia Congenita,,,,DOID:0050449,pachyonychia congenita,C1706595,D053549,167200,MONDO:0008173,pachyonychia congenita 1,
+BMGC_DS09741,BMG_DS037142,,,,,,,DOID:7902,adult extraskeletal myxoid chondrosarcoma,C1706731,,,MONDO:0003899,adult myxoid chondrosarcoma,
+BMGC_DS09742,BMG_DS037143,,,,,,,,,C1706762,,,MONDO:0016505,aldosterone-producing adrenal cortex adenoma,
+BMGC_DS09743,BMG_DS037147,,,,,,,DOID:0060463,NUT midline carcinoma,C1707291,,,MONDO:0005563,nut midline carcinoma,
+BMGC_DS09744,BMG_DS037150,,,,,,,,,C1707400,,,MONDO:0016712,classic medulloblastoma,
+BMGC_DS09745,BMG_DS037164,,,,,,,,,C1708349,,,MONDO:0007648,hereditary diffuse gastric adenocarcinoma,
+BMGC_DS09746,BMG_DS037165,,,,,,,,,C1708350,,150800,MONDO:0007888,hereditary leiomyomatosis and renal cell cancer,
+BMGC_DS09747,BMG_DS037166,,,,,,,,,C1708353,,,MONDO:0017366,hereditary pheochromocytoma-paraganglioma,
+BMGC_DS09748,BMG_DS037168,,,,,,,,,C1708371,,500000,MONDO:0010771,histiocytoid cardiomyopathy,
+BMGC_DS09749,BMG_DS037177,,,,,,,,,C1708781,,,MONDO:0006279,lung sarcomatoid carcinoma,
+BMGC_DS09750,BMG_DS037185,,Osteofibrous Dysplasia,,,,,,,C1709353,C563276,,,,
+BMGC_DS09751,BMG_DS037198,,,,,,,,,C1710096,,,MONDO:0006411,sinonasal undifferentiated carcinoma,
+BMGC_DS09752,BMG_DS037203,,Familial spinal arachnoiditis,,,,,,,C1710146,C531624,182950,MONDO:0008450,spinal arachnoiditis,
+BMGC_DS09753,BMG_DS037208,,,,,,,DOID:0070327,melanoma in congenital melanocytic nevus,C1711221,,,MONDO:0850110,melanoma in congenital melanocytic nevus,
+BMGC_DS09754,BMG_DS037220,433493000,Acquired torsion dystonia,,,,,,,C1719382,,,MONDO:0044870,acquired torsion dystonia,Acquired torsion dystonia (disorder) | Acquired torsion dystonia
+BMGC_DS09755,BMG_DS037224,425756000,Idiopathic transverse myelitis,,,,,,,C1719404,,,,,Idiopathic transverse myelitis (disorder) | Idiopathic transverse myelitis
+BMGC_DS09756,BMG_DS037249,,Severe Sepsis,Sepsis,,,,,,C1719672,D018805,,,,
+BMGC_DS09757,BMG_DS037262,421182009,Episodic ataxia type 1,,,,,,,C1719788,,160120,MONDO:0008047,episodic ataxia type 1,Episodic ataxia type 1 (disorder) | Episodic ataxia type 1 | Episodic ataxia type 1 (EA1)
+BMGC_DS09758,BMG_DS037279,420585007,Meningitis caused by Klebsiella aerogenes,,,,,,,C1719906,,,,,Meningitis caused by Klebsiella mobilis | Meningitis caused by Enterobacter aerogenes | Meningitis caused by Aerobacter aerogenes | Meningitis caused by Klebsiella aerogenes | Meningitis caused by Klebsiella aerogenes (disorder)
+BMGC_DS09759,BMG_DS037284,422014003,Disorder due to type 2 diabetes mellitus,,,,,,,C1719939,,,,,Disorder due to type 2 diabetes mellitus (disorder) | Disorder due to type 2 diabetes mellitus | Disorder due to type II diabetes mellitus
+BMGC_DS09760,BMG_DS037305,421429008,Gastrointestinal infection caused by Klebsiella aerogenes,,,,,,,C1720135,,,,,Gastrointestinal infection caused by Klebsiella mobilis | Gastrointestinal infection caused by Enterobacter aerogenes | Gastrointestinal infection caused by Aerobacter aerogenes | Gastrointestinal infection caused by Klebsiella aerogenes | Gastrointestinal infection caused by Klebsiella aerogenes (disorder)
+BMGC_DS09761,BMG_DS037309,422127002,Herpes zoster with AIDS (acquired immunodeficiency syndrome),,,,,,,C1720144,,,,,Herpes zoster with acquired immunodeficiency syndrome (disorder) | Herpes zoster with AIDS (acquired immunodeficiency syndrome) | Herpes zoster with acquired immunodeficiency syndrome
+BMGC_DS09762,BMG_DS037318,,Episodic Ataxia,,,,,DOID:963,episodic ataxia,C1720189,C580065,,MONDO:0016227,hereditary episodic ataxia,
+BMGC_DS09763,BMG_DS037342,,"Episodic Ataxia, Type 2",,,,,DOID:0050990,episodic ataxia type 2,C1720416,C535506,108500,MONDO:0007163,episodic ataxia type 2,
+BMGC_DS09764,BMG_DS037352,421666009,Toxoplasmosis associated with acquired immunodeficiency syndrome,,,,,,,C1720498,,,,,Toxoplasmosis associated with AIDS | Toxoplasmosis associated with acquired immunodeficiency syndrome (disorder) | Toxoplasmosis associated with acquired immunodeficiency syndrome
+BMGC_DS09765,BMG_DS037353,421684006,Adult growth hormone deficiency,,,,,,,C1720505,,,,,Adult growth hormone deficiency (disorder) | Adult growth hormone deficiency
+BMGC_DS09766,BMG_DS037381,,,,,,,,,C1720771,,,MONDO:0004920,hydrocele,
+BMGC_DS09767,BMG_DS037382,,Hypoprebetalipoproteinemia,Hypolipoproteinemias,,,,,,C1720772,D007009,,,,
+BMGC_DS09768,BMG_DS037383,,Glomerular Necrosis,Kidney Cortex Necrosis,,,,,,C1720774,D007673,,,,
+BMGC_DS09769,BMG_DS037385,,,,,,,DOID:0111418,familial apolipoprotein C-II deficiency,C1720779,,207750,MONDO:0008810,familial apolipoprotein C-II deficiency,
+BMGC_DS09770,BMG_DS037386,,"Meningitis, Pneumococcal, Recurrent","Meningitis, Pneumococcal",,,,,,C1720785,D008586,,,,
+BMGC_DS09771,BMG_DS037387,,Acute Bacterial Prostatitis,Prostatitis,,,,,,C1720795,D011472,,,,
+BMGC_DS09772,BMG_DS037388,,Asymptomatic Inflammatory Prostatitis,Prostatitis,,,,,,C1720796,D011472,,,,
+BMGC_DS09773,BMG_DS037389,,Chronic Bacterial Prostatitis,Prostatitis,,,,,,C1720797,D011472,,,,
+BMGC_DS09774,BMG_DS037390,,"Refsum Disease, Phytanoyl-CoA Hydroxylase Deficiency",Refsum Disease,,,,,,C1720802,D012035,,,,
+BMGC_DS09775,BMG_DS037392,,Endometrial Diseases,Uterine Diseases,,,,,,C1720816,D014591,,,,
+BMGC_DS09776,BMG_DS037393,,"Membranoproliferative Glomerulonephritis, Type III","Glomerulonephritis, Membranoproliferative",,,,,,C1720821,D015432,,,,
+BMGC_DS09777,BMG_DS037394,,,,,,,,,C1720824,,,MONDO:0100511,sudden cardiac arrest,
+BMGC_DS09778,BMG_DS037395,,Painful Bladder Syndrome,"Cystitis, Interstitial",,,,,,C1720830,D018856,,,,
+BMGC_DS09779,BMG_DS037397,,"Familial Partial Lipodystrophy, Type 1","Lipodystrophy, Familial Partial",,,,DOID:0070207;DOID:0050440,familial partial lipodystrophy type 1 | familial partial lipodystrophy,C1720859,D052496,608600,MONDO:0012072,"familial partial lipodystrophy, Kobberling type",
+BMGC_DS09780,BMG_DS037398,,"Familial Partial Lipodystrophy, Type 2","Lipodystrophy, Familial Partial",,,,DOID:0070202;DOID:0050440,familial partial lipodystrophy type 2 | familial partial lipodystrophy,C1720860,D052496,151660,MONDO:0007906,"familial partial lipodystrophy, Dunnigan type",
+BMGC_DS09781,BMG_DS037399,,"Familial Partial Lipodystrophy, Type 3","Lipodystrophy, Familial Partial",,,,DOID:0070204;DOID:0050440,familial partial lipodystrophy type 3 | familial partial lipodystrophy,C1720861,D052496,604367,MONDO:0011448,PPARG-related familial partial lipodystrophy,
+BMGC_DS09782,BMG_DS037400,,Congenital Generalized Lipodystrophy Type 1,"Lipodystrophy, Congenital Generalized",,,,,,C1720862,D052497,608594,MONDO:0012071,congenital generalized lipodystrophy type 1,
+BMGC_DS09783,BMG_DS037401,,,,,,,,,C1720863,,269700,MONDO:0010020,congenital generalized lipodystrophy type 2,
+BMGC_DS09784,BMG_DS037402,,"Sulfatidosis, Juvenile, Austin Type",Multiple Sulfatase Deficiency Disease,,,,DOID:0050441,mucosulfatidosis,C1720864,D052517,,,,
+BMGC_DS09785,BMG_DS037403,,Female Urogenital Diseases,Female Urogenital Diseases,,,,,,C1720887,D052776,,,,
+BMGC_DS09786,BMG_DS037404,,Male Urogenital Diseases,Male Urogenital Diseases,,,,,,C1720894,D052801,,,,
+BMGC_DS09787,BMG_DS037405,,"Hyper-IgM Immunodeficiency Syndrome, Type 2",Hyper-IgM Immunodeficiency Syndrome,,,,DOID:0060758,immunodeficiency with hyper-IgM type 2,C1720956,D053306,605258,MONDO:0011528,hyper-IgM syndrome type 2,
+BMGC_DS09788,BMG_DS037406,,"Hyper-IgM Immunodeficiency Syndrome, Type 3",Hyper-IgM Immunodeficiency Syndrome,,,,DOID:0060023,immunodeficiency with hyper IgM type 3,C1720957,D053306,606843,MONDO:0011735,hyper-IgM syndrome type 3,
+BMGC_DS09789,BMG_DS037407,,"Hyper-IgM Immunodeficiency Syndrome, Type 5",Hyper-IgM Immunodeficiency Syndrome,,,,DOID:0060759,immunodeficiency with hyper IgM type 5,C1720958,D053306,608106,MONDO:0011971,hyper-IgM syndrome type 5,
+BMGC_DS09790,BMG_DS037408,,"Ectodermal Dysplasia 3, Anhidrotic","Ectodermal Dysplasia 3, Anhidrotic",,,,,,C1720965,D053359,,,,
+BMGC_DS09791,BMG_DS037409,,Channelopathies,Channelopathies,,,,,,C1720983,D053447,,MONDO:0021016,obsolete channelopathy,
+BMGC_DS09792,BMG_DS037411,,"Leukokeratosis, Hereditary Mucosal","Leukokeratosis, Hereditary Mucosal",,,,DOID:0050448,white sponge nevus,C1721005,D053529,,MONDO:0015748,hereditary mucosal leukokeratosis,
+BMGC_DS09793,BMG_DS037412,,"Keratoderma, Palmoplantar, Epidermolytic","Keratoderma, Palmoplantar, Epidermolytic",,,,DOID:0080223,epidermolytic palmoplantar keratoderma,C1721006,D053546,,MONDO:0968949,"palmoplantar keratoderma, epidermolytic",
+BMGC_DS09794,BMG_DS037413,,"Pachyonychia Congenita, Type 2",Pachyonychia Congenita,,,,DOID:0050449,pachyonychia congenita,C1721007,D053549,167210,MONDO:0008174,pachyonychia congenita 2,
+BMGC_DS09795,BMG_DS037415,,Paraneoplastic Opsoclonus-Myoclonus Ataxia,Opsoclonus-Myoclonus Syndrome,,,,,,C1721017,D053578,,,,
+BMGC_DS09796,BMG_DS037417,,,,,,,DOID:0050451,Brugada syndrome,C1721096,,,,,
+BMGC_DS09797,BMG_DS037418,,Chronic Prostatitis with Chronic Pelvic Pain Syndrome,Prostatitis,,,,,,C1723764,D011472,,,,
+BMGC_DS09798,BMG_DS037420,,Migraine with Typical Aura,Migraine with Aura,,,,,,C1735856,D020325,,,,
+BMGC_DS09799,BMG_DS037423,,Bland White Garland Syndrome,Bland White Garland Syndrome,,,,DOID:0060562,anomalous left coronary artery from the pulmonary artery,C1735886,D063748,,MONDO:0000811,anomalous left coronary artery from the pulmonary artery,
+BMGC_DS09800,BMG_DS037434,,Latent Autoimmune Diabetes in Adults,Latent Autoimmune Diabetes in Adults,,,,DOID:0080846,latent autoimmune diabetes in adults,C1739108,D000071698,,MONDO:0850306,latent autoimmune diabetes in adults,
+BMGC_DS09801,BMG_DS037436,,Prostatic Hypertrophy,Prostatic Hyperplasia,,,,,,C1739363,D011470,,,,
+BMGC_DS09802,BMG_DS037437,,,,,,,,,C1739384,,105835,MONDO:0007114,Angel-shaped phalango-epiphyseal dysplasia,
+BMGC_DS09803,BMG_DS037438,,Takotsubo Cardiomyopathy,Takotsubo Cardiomyopathy,,,,,,C1739395,D054549,,MONDO:0019018,Tako-tsubo cardiomyopathy,
+BMGC_DS09804,BMG_DS037442,239051001,Congenital ectodermal dysplasia of face,,,,,,,C1744559,,227260,MONDO:0009203,focal facial dermal dysplasia type III,Congenital ectodermal dysplasia of face | Congenital ectodermal dysplasia of face (disorder)
+BMGC_DS09805,BMG_DS037446,155597006;47839005,Aspiration pneumonitis,,,,,,,C1761609,,,MONDO:0002572,aspiration pneumonitis,Aspiration pneumonitis | Aspiration pneumonitis (disorder) | Aspiration pneumonia | Inhalation pneumonia | Aspiration pneumonitis | Aspiration pneumonia (disorder)
+BMGC_DS09806,BMG_DS037447,,RAPP-HODGKIN SYNDROME,,,,,DOID:0090119,ankyloblepharon-ectodermal defects-cleft lip/palate syndrome,C1785148,,129400;603273,MONDO:0007508,Rapp-Hodgkin syndrome,
+BMGC_DS09807,BMG_DS037448,,Idiopathic Pulmonary Fibrosis,Idiopathic Pulmonary Fibrosis,,,,DOID:0050156,idiopathic pulmonary fibrosis,C1800706,D054990,,,,
+BMGC_DS09808,BMG_DS037449,55016009,Congenital muscular hypertrophy-cerebral syndrome,,,,,,,C1802395,,300590,MONDO:0010370,Cornelia de Lange syndrome 2,Congenital muscular hypertrophy-cerebral syndrome | Bruch-de Lange syndrome | Congenital muscular hypertrophy-cerebral syndrome (disorder)
+BMGC_DS09809,BMG_DS037452,237885008;190868007;54920000,Familial benign hypercalcemia,,,,,,,C1809471,,,MONDO:0018458,familial hypocalciuric hypercalcemia,Familial hypocalciuric hypercalcaemia | Familial hypocalciuric hypercalcemia | Familial hypocalciuric hypercalcemia (disorder) | Familial benign hypercalcaemia | Familial benign hypercalcemia | FHH - familial hypocalciuric hypercalcaemia | FHH - familial hypocalciuric hypercalcemia | Familial benign hypercalcemia | Familial benign hypercalcaemia | Familial benign hypercalcemia (disorder) | Familial hyperparathyroidism | Familial hyperparathyroidism (disorder)
+BMGC_DS09810,BMG_DS037454,47452006;266193008;154344005,Variola major,,,,,DOID:0050508,variola major,C1812609,,,MONDO:0000338,variola major infectious disease,Variola major | Classical smallpox | Variola major (disorder) | Ordinary smallpox | Pseudocowpox | Fifth disease | Other viral exanthemata | Roseola infantum | Variola major | Cowpox | Parascarlatina | Fourth disease | Milkers' node | Milker's node | Smallpox | Orf | (Viral exanthemata [& variants]) or (orf) or (milkers node) | (Viral exanthemata [& variants]) or (orf) or (milkers node) (disorder) | Cowpox | Milker's node | Smallpox | Orf | Roseola infantum | Variola major | Other viral exanthemata | Fourth disease | Milkers' node | Fifth disease | Parascarlatina | Pseudocowpox | (Viral exanthemata [& variants]) or (orf) or (milkers node) | (Viral exanthemata [& variants]) or (orf) or (milkers node) (disorder)
+BMGC_DS09811,BMG_DS037455,,"DEAFNESS, AUTOSOMAL RECESSIVE 70",,,,,,,C1824925,,610316;614934,MONDO:0013978,autosomal recessive nonsyndromic hearing loss 70,
+BMGC_DS09812,BMG_DS037478,424404003,Decompensated chronic heart failure,,,,,,,C1827266,,,,,Decompensated chronic heart failure (disorder) | Decompensated chronic heart failure
+BMGC_DS09813,BMG_DS037482,,Extensively Drug-Resistant Tuberculosis,Extensively Drug-Resistant Tuberculosis,,,,,,C1827301,D054908,,MONDO:0100482,extensively drug-resistant tuberculosis,
+BMGC_DS09814,BMG_DS037488,424451001,Poor metabolizer due to cytochrome p450 CYP2C9 variant,,,,,,,C1827367,,,,,Poor metabolizer due to cytochrome p450 CYP2C9 variant (disorder) | Poor metabolizer due to cytochrome p450 CYP2C9 variant | Poor metabolizer due to CYP2C9
+BMGC_DS09815,BMG_DS037492,425079005,Slow acetylator due to N-acetyltransferase enzyme variant,,,,,,,C1827377,,,,,Slow acetylator due to N-acetyltransferase enzyme variant (disorder) | Slow acetylator due to N-acetyltransferase enzyme variant | Slow acetylator
+BMGC_DS09816,BMG_DS037499,424500005,Poor metabolizer due to cytochrome p450 CYP2C19 variant,,,,,,,C1827468,,,,,Poor metabolizer due to cytochrome p450 CYP2C19 variant (disorder) | Poor metabolizer due to cytochrome p450 CYP2C19 variant | Poor metabolizer due to CYP2C19
+BMGC_DS09817,BMG_DS037525,422681000,Ultrarapid metabolizer due to cytochrome p450 CYP2D6 variant,,,,,,,C1827786,,,,,Ultrarapid metabolizer due to cytochrome p450 CYP2D6 variant (disorder) | Ultrarapid metabolizer due to cytochrome p450 CYP2D6 variant | Ultrarapid metabolizer due to CYP2D6
+BMGC_DS09818,BMG_DS037547,,,,,,,,,C1828066,,264060,MONDO:0009907,Prepapillary vascular loops,
+BMGC_DS09819,BMG_DS037558,,"Macular dystrophy, concentric annular",,,,,,,C1828210,C537833,,,,
+BMGC_DS09820,BMG_DS037573,423629005,Poor metabolizer due to cytochrome p450 CYP2D6 variant,,,,,,,C1828413,,,,,Poor metabolizer due to cytochrome p450 CYP2D6 variant (disorder) | Poor metabolizer due to cytochrome p450 CYP2D6 variant | Poor metabolizer due to CYP2D6
+BMGC_DS09821,BMG_DS037582,,Carnitine palmitoyl transferase 1A deficiency,,,,,,,C1829703,C535588,255120,MONDO:0009705,carnitine palmitoyl transferase 1A deficiency,
+BMGC_DS09822,BMG_DS037584,,,,,,,,,C1832099,,601583,MONDO:0011112,Wilms tumor 5,
+BMGC_DS09823,BMG_DS037587,,"HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY",,,,,DOID:0110711,congenital hypotrichosis with juvenile macular dystrophy,C1832162,,601553;114021,MONDO:0011107,congenital hypotrichosis with juvenile macular dystrophy,
+BMGC_DS09824,BMG_DS037588,,"Ectopia Lentis, Spontaneous Filtering Blebs, and Craniofacial Dysmorphism",,,,,,,C1832167,C563293,601552,MONDO:0011106,facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome,
+BMGC_DS09825,BMG_DS037589,,DOYNE HONEYCOMB RETINAL DYSTROPHY,,,,,,,C1832174,,126600;601548,MONDO:0007471,Doyne honeycomb retinal dystrophy,
+BMGC_DS09826,BMG_DS037590,,"Cataract, Congenital, Cerulean Type, 2",,,,,,,C1832175,C563294,601547,MONDO:0011104,cataract 3 multiple types,
+BMGC_DS09827,BMG_DS037591,,"Deafness, Autosomal Dominant 12",,,,,,,C1832187,C563295,601543,MONDO:0011102,autosomal dominant nonsyndromic hearing loss 12,
+BMGC_DS09828,BMG_DS037592,,Peroxisome biogenesis disorders,,,,,,,C1832200,C536664,,MONDO:0019234,peroxisome biogenesis disorder,
+BMGC_DS09829,BMG_DS037594,,Athabaskan brainstem dysgenesis,,,,,,,C1832215,C535397,601536,MONDO:0011099,human HOXA1 syndromes,
+BMGC_DS09830,BMG_DS037595,,Bosley-Salih-Alorainy Syndrome,,,,,,,C1832216,C535397,,MONDO:0019075,Bosley-Salih-Alorainy syndrome,
+BMGC_DS09831,BMG_DS037596,,Rieger syndrome 2,,,,,,,C1832229,C535680,601499,MONDO:0011097,Axenfeld-Rieger syndrome type 2,
+BMGC_DS09832,BMG_DS037600,,"Agammaglobulinemia, non-Bruton type",,,,,,,C1832241,C538056,,MONDO:0011096,autosomal agammaglobulinemia,
+BMGC_DS09833,BMG_DS037601,,"Cardiomyopathy, Dilated, 1D",,,,,,,C1832243,C563306,601494,MONDO:0011095,dilated cardiomyopathy 1D,
+BMGC_DS09834,BMG_DS037602,,"Cardiomyopathy, Dilated, 1C",,,,,,,C1832244,C563307,601493,MONDO:0011094,dilated cardiomyopathy 1C,
+BMGC_DS09835,BMG_DS037603,,Ribbing disease,,,,,,,C1832273,C537613,601477,MONDO:0011092,ribbing disease,
+BMGC_DS09836,BMG_DS037604,,"Charcot-Marie-Tooth disease, Type 2D",,,,,,,C1832274,C537993,601472,MONDO:0011091,Charcot-Marie-Tooth disease type 2D,
+BMGC_DS09837,BMG_DS037605,,"FACIAL PARESIS, HEREDITARY CONGENITAL, 1",,,,,,,C1832284,,601471,MONDO:0024466,"facial paresis, hereditary congenital, 1",
+BMGC_DS09838,BMG_DS037607,,"Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive",,,,,DOID:0090013,"severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive",C1832322,C563311,601457,MONDO:0011086,"severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive",
+BMGC_DS09839,BMG_DS037608,,"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D",,,,,,,C1832334,,601455;605262,MONDO:0011085,Charcot-Marie-Tooth disease type 4D,
+BMGC_DS09840,BMG_DS037612,,"Deafness, Progressive, With Stapes Fixation",,,,,,,C1832354,C563316,601449,MONDO:0011080,progressive deafness with stapes fixation,
+BMGC_DS09841,BMG_DS037613,715505002,Rhizomelic dysplasia Patterson Lowry type,,,,,,,C1832359,C537609,601438,MONDO:0011079,"rhizomelic dysplasia, Patterson-Lowry type",Rhizomelic dysplasia of Patterson Lowry type (disorder) | Rhizomelic dysplasia of Patterson Lowry type | Rhizomelic dysplasia Patterson Lowry type
+BMGC_DS09842,BMG_DS037614,,Jung Wolff Back Stahl syndrome,,,,,,,C1832362,C537694,601427,MONDO:0011078,"anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis",
+BMGC_DS09843,BMG_DS037616,,"MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED",,,,,,,C1832370,,601419;601419;615325,MONDO:0011076,myofibrillar myopathy 1,
+BMGC_DS09844,BMG_DS037617,,Retinitis Pigmentosa 18,,,,,DOID:0110356,retinitis pigmentosa 18,C1832378,C563320,601414,MONDO:0011075,retinitis pigmentosa 18,
+BMGC_DS09845,BMG_DS037618,,"Deafness, Autosomal Dominant 7",,,,,,,C1832379,C563321,601412,MONDO:0011074,autosomal dominant nonsyndromic hearing loss 7,
+BMGC_DS09846,BMG_DS037619,,"Diabetes Mellitus, Transient Neonatal, 1",,,,,,,C1832386,C563322,601410,MONDO:0011073,"diabetes mellitus, transient neonatal, 1",
+BMGC_DS09847,BMG_DS037621,,"Platelet Disorder, Familial, with Associated Myeloid Malignancy",,,,,,,C1832388,C563324,601399,MONDO:0100083;MONDO:0011071,hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | hereditary thrombocytopenia and hematologic cancer predisposition syndrome,
+BMGC_DS09848,BMG_DS037622,,Van Maldergem Wetzburger Verloes syndrome,,,,,DOID:0060238,Van Maldergem syndrome,C1832390,C536530,,MONDO:0017813,van Maldergem syndrome,
+BMGC_DS09849,BMG_DS037623,,Cervical ribs sprengel anomaly anal atresia urethral obstruction,,,,,,,C1832391,C538072,601389,MONDO:0011069,"cervical ribs, Sprengel anomaly, anal atresia, and urethral obstruction",
+BMGC_DS09850,BMG_DS037624,,"DIABETES MELLITUS, INSULIN-DEPENDENT, 12",,,,,,,C1832392,,601388,MONDO:0011068,type 1 diabetes mellitus 12,
+BMGC_DS09851,BMG_DS037625,,"Deafness, Autosomal Recessive 12",,,,,,,C1832394,C563327,601386,MONDO:0011067,autosomal recessive nonsyndromic hearing loss 12,
+BMGC_DS09852,BMG_DS037626,,"Charcot-Marie-Tooth disease, Type 4B1",,,,,DOID:0110191,Charcot-Marie-Tooth disease type 4B1,C1832399,C535420,601382,MONDO:0011066,Charcot-Marie-Tooth disease type 4B1,
+BMGC_DS09853,BMG_DS037627,,Hunter-McAlpine craniosynostosis syndrome,,,,,,,C1832408,C536072,601379,MONDO:0011065,Hunter-McAlpine craniosynostosis,
+BMGC_DS09854,BMG_DS037628,702363009;725097006,Crisponi syndrome,,,,,DOID:0060294,cold-induced sweating syndrome,C1832409,C536214,,MONDO:0015526,cold-induced sweating syndrome,Cold-induced sweating syndrome (disorder) | Cold-induced sweating syndrome | Ciliary neurotrophic factor receptor-related disorder | Sohar-Crisponi syndrome | Crisponi syndrome (disorder) | Crisponi syndrome
+BMGC_DS09855,BMG_DS037631,,Aprosencephaly and Cerebellar Dysgenesis,,,,,,,C1832412,C563331,601374,MONDO:0011062,aprosencephaly cerebellar dysgenesis,
+BMGC_DS09856,BMG_DS037633,,,,,,,,,C1832423,,601371,MONDO:0011060,early-onset non-syndromic cataract,
+BMGC_DS09857,BMG_DS037634,715434005,Genoa syndrome,,,,,,,C1832424,C537684,601370,MONDO:0011059,holoprosencephaly-craniosynostosis syndrome,Holoprosencephaly craniosynostosis syndrome (disorder) | Holoprosencephaly craniosynostosis syndrome | Camero Lituania Cohen syndrome | Genoa syndrome
+BMGC_DS09858,BMG_DS037635,,"Deafness, Autosomal Dominant 9",,,,,,,C1832425,C563335,601369,MONDO:0011058,autosomal dominant nonsyndromic hearing loss 9,
+BMGC_DS09859,BMG_DS037636,,,,,,,,,C1832426,,601363,MONDO:0011056,Wilms tumor 4,
+BMGC_DS09860,BMG_DS037637,,Digeorge Syndrome-Velocardiofacial Syndrome Complex 2,,,,,,,C1832431,C563337,601362,MONDO:0011055,distal monosomy 10p,
+BMGC_DS09861,BMG_DS037638,,"Amelia, Autosomal Recessive",,,,,,,C1832432,C563338,601360,MONDO:0011054,autosomal recessive amelia,
+BMGC_DS09862,BMG_DS037640,,Yim Ebbin syndrome,,,,,,,C1832434,C536713,601357,MONDO:0011052,amelia cleft lip palate hydrocephalus iris coloboma,
+BMGC_DS09863,BMG_DS037641,,Short limb dwarfism Al Gazali type,,,,,,,C1832435,C537598,601356,MONDO:0011051,"lethal short-limb skeletal dysplasia, Al Gazali type",
+BMGC_DS09864,BMG_DS037642,,"Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs",,,,,,,C1832436,C563341,601355,MONDO:0011050,microcephaly-cardiac defect-lung malsegmentation syndrome,
+BMGC_DS09865,BMG_DS037643,,"Mental Retardation, Microcephaly, Epilepsy, And Coarse Face",,,,,,,C1832437,C563342,601352,MONDO:0011048,epilepsy-microcephaly-skeletal dysplasia syndrome,
+BMGC_DS09866,BMG_DS037646,,"MICROPHTHALMIA, SYNDROMIC 8",,,,,DOID:0111803,syndromic microphthalmia 8,C1832440,,601349,MONDO:0011045,MMEP syndrome,
+BMGC_DS09867,BMG_DS037649,,Martinez-Frias Syndrome,,,,,,,C1832443,C563346,601346,MONDO:0011042,Martinez-Frias syndrome,
+BMGC_DS09868,BMG_DS037650,,"Ectodermal Dysplasia with Natal Teeth, Turnpenny Type",,,,,,,C1832444,C563347,601345,MONDO:0011041,"ectodermal dysplasia with natal teeth, Turnpenny type",
+BMGC_DS09869,BMG_DS037651,,"Spinal Dysplasia, Anhalt Type",,,,,,,C1832464,C563348,601344,MONDO:0011040,"spinal dysplasia, Anhalt type",
+BMGC_DS09870,BMG_DS037652,,"Atrophia Maculosa Varioliformis Cutis, Familial",,,,,,,C1832465,C563349,601341,MONDO:0011039,"atrophia maculosa varioliformis cutis, familial",
+BMGC_DS09871,BMG_DS037653,,CAPOS syndrome,,,,,,,C1832466,C535351,601338,MONDO:0011038,cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome,
+BMGC_DS09872,BMG_DS037655,,Porencephaly cerebellar hypoplasia malformations,,,,,,,C1832472,C536336,601322,MONDO:0011036,porencephaly-cerebellar hypoplasia-internal malformations syndrome,
+BMGC_DS09873,BMG_DS037656,,Odontomicronychial dysplasia,,,,,,,C1832473,C537741,601319,MONDO:0011034,odontomicronychial dysplasia,
+BMGC_DS09874,BMG_DS037658,,"Deafness, Autosomal Dominant 11",,,,,,,C1832475,C563353,601317,MONDO:0011032,autosomal dominant nonsyndromic hearing loss 11,
+BMGC_DS09875,BMG_DS037659,,"Deafness, Autosomal Dominant 10",,,,,,,C1832476,C563354,601316,MONDO:0011031,autosomal dominant nonsyndromic hearing loss 10,
+BMGC_DS09876,BMG_DS037662,,Limb-girdle muscular dystrophy type 2F,,,,,,,C1832525,C535896,601287,MONDO:0011028,autosomal recessive limb-girdle muscular dystrophy type 2F,
+BMGC_DS09877,BMG_DS037664,,"Diabetes Mellitus, Noninsulin-Dependent, 1",,,,,,,C1832544,C563359,601283,MONDO:0011027,"diabetes mellitus, noninsulin-dependent, 1",
+BMGC_DS09878,BMG_DS037665,,,,,,,,,C1832550,,601277,MONDO:0011026,autosomal recessive congenital ichthyosis 4A,
+BMGC_DS09879,BMG_DS037666,,Rippling Muscle Disease 2,,,,,DOID:0070308,rippling muscle disease 1,C1832560,C535686,606072,MONDO:0019947,rippling muscle disease 2,
+BMGC_DS09880,BMG_DS037667,,"CEREBELLAR ATAXIA, CAYMAN TYPE",,,,,,,C1832585,,601238,MONDO:0011025,Cayman type cerebellar ataxia,
+BMGC_DS09881,BMG_DS037668,,"DERMATITIS HERPETIFORMIS, FAMILIAL",,,,,,,C1832586,,601230,MONDO:0011024,"dermatitis herpetiformis, familial",
+BMGC_DS09882,BMG_DS037669,,"POLYPOSIS SYNDROME, HEREDITARY MIXED, 1",,,,,DOID:0111685,hereditary mixed polyposis syndrome 1,C1832587,,601228,MONDO:0042486,"polyposis syndrome, hereditary mixed, 1",
+BMGC_DS09883,BMG_DS037670,,Chromosome 11p11.2 Deletion Syndrome,,,,,DOID:0111687,Potocki-Shaffer syndrome,C1832588,C538356,601224,MONDO:0011022,Potocki-Shaffer syndrome,
+BMGC_DS09884,BMG_DS037671,,"Neuronal Intestinal Dysplasia, Type B",,,,,,,C1832589,C537394,601223,MONDO:0011021,"neuronal intestinal dysplasia, type B",
+BMGC_DS09885,BMG_DS037675,716195006,Verloes Bourguignon syndrome,,,,,,,C1832594,C536538,601216,MONDO:0011018,brachyolmia-amelogenesis imperfecta syndrome,Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome (disorder) | Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome | Platyspondyly amelogenesis imperfecta | Verloes Bourguignon syndrome | Brachyolmia and amelogenesis imperfecta syndrome
+BMGC_DS09886,BMG_DS037676,715535009,Naxos disease,,,,,DOID:0080551,Naxos disease,C1832600,C538346,601214,MONDO:0011017,Naxos disease,Naxos disease | Keratoderma with woolly hair type I | Keratoderma with wooly hair type I | Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome (disorder) | Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome | Palmoplantar hyperkeratosis with arrhythmogenic cardiomyopathy
+BMGC_DS09887,BMG_DS037678,,Anterior polar cataract 2,,,,,,,C1832609,C537774,601202,MONDO:0011015,cataract 24,
+BMGC_DS09888,BMG_DS037680,,"Hypocalcemia, Autosomal Dominant, with Bartter Syndrome",,,,,,,C1832612,C563374,,,,
+BMGC_DS09889,BMG_DS037681,,"HYPERPARATHYROIDISM, NEONATAL SEVERE",,,,,,,C1832615,,601199;239200,MONDO:0009397,neonatal severe primary hyperparathyroidism,
+BMGC_DS09890,BMG_DS037682,,Hypoparathyroidism familial isolated,,,,,,,C1832648,C537156,,MONDO:0016390,familial hypoparathyroidism,
+BMGC_DS09891,BMG_DS037683,,Anophthalmia with pulmonary hypoplasia,,,,,DOID:0111807,syndromic microphthalmia 9,C1832661,C537768,601186,MONDO:0011010,Matthew-Wood syndrome,
+BMGC_DS09892,BMG_DS037684,,,,,,,,,C1832662,,608446,MONDO:0012039,"myocardial infarction, susceptibility to",
+BMGC_DS09893,BMG_DS037686,,"Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects Of Skull",,,,,,,C1832668,C563380,601163,MONDO:0011007,diaphragmatic defect-limb deficiency-skull defect syndrome,
+BMGC_DS09894,BMG_DS037687,,"Spastic paraplegia 9, autosomal dominant",,,,,,,C1832669,C536868,,MONDO:0015091,autosomal dominant spastic paraplegia type 9,
+BMGC_DS09895,BMG_DS037690,,"CARDIOMYOPATHY, DILATED, 1E",,,,,,,C1832680,,601154;600163,MONDO:0011003,dilated cardiomyopathy 1E,
+BMGC_DS09896,BMG_DS037691,,,,,,,DOID:0110965,brachydactyly type A2,C1832702,,112600,MONDO:0007216,brachydactyly type A2,
+BMGC_DS09897,BMG_DS037692,,MULTIPLE SYNOSTOSES SYNDROME 2,,,,,DOID:0081318,multiple synostoses syndrome 2,C1832708,,601146;610017,MONDO:0012394,multiple synostoses syndrome 2,
+BMGC_DS09898,BMG_DS037693,,Fallot complex with severe mental and growth retardation,,,,,,,C1832735,C536608,601127,MONDO:0010999,fallot complex-intellectual disability-growth delay syndrome,
+BMGC_DS09899,BMG_DS037694,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id",,,,,DOID:0080556,congenital disorder of glycosylation Id,C1832736,,601110;608750,MONDO:0010998,ALG3-congenital disorder of glycosylation,
+BMGC_DS09900,BMG_DS037697,,"Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation",,,,,DOID:0111688,Ayme-Gripp syndrome,C1832812,C563390,601088,MONDO:0010992,Ayme-Gripp syndrome,
+BMGC_DS09901,BMG_DS037698,,"Laterality Defects, Autosomal Dominant",,,,,,,C1832813,C563391,601086,MONDO:0010991,"laterality defects, autosomal dominant",
+BMGC_DS09902,BMG_DS037699,,"Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction",,,,,,,C1832826,C563394,601075,MONDO:0010988,aplasia cutis-myopia syndrome,
+BMGC_DS09903,BMG_DS037700,,"DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8",,,,,,,C1832827,,601072,MONDO:0010987,autosomal recessive nonsyndromic hearing loss 8,
+BMGC_DS09904,BMG_DS037701,,"Deafness, Autosomal Recessive 9",,,,,,,C1832828,C563396,601071,MONDO:0010986,autosomal recessive nonsyndromic hearing loss 9,
+BMGC_DS09905,BMG_DS037703,,"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1",,,,,DOID:0111690,familial adult myoclonic epilepsy 1,C1832841,,601068;618073,MONDO:0010985,"epilepsy, familial adult myoclonic, 1",
+BMGC_DS09906,BMG_DS037704,,"USHER SYNDROME, TYPE ID",,,,,,,C1832845,,601067;605516,MONDO:0010984,Usher syndrome type 1D,
+BMGC_DS09907,BMG_DS037705,,"CHOREOATHETOSIS/SPASTICITY, EPISODIC",,,,,DOID:0090044,dystonia 9,C1832855,,601042,MONDO:0010983,dystonia 9,
+BMGC_DS09908,BMG_DS037706,,Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin,,,,,,,C1832858,C563402,601039,MONDO:0010982,ichthyosis-intellectual disability syndrome with large keratohyalin granules in the skin,
+BMGC_DS09909,BMG_DS037709,,"Hemiplegic migraine, familial type 1",,,,,,,C1832884,C536890,141500,MONDO:0020756,"migraine, familial hemiplegic, 1",
+BMGC_DS09910,BMG_DS037710,,"MIGRAINE, SPORADIC HEMIPLEGIC",,,,,DOID:0111181,familial hemiplegic migraine 1,C1832903,,601011;141500,MONDO:0020757,sporadic hemiplegic migraine,
+BMGC_DS09911,BMG_DS037711,1230096008,Timothy syndrome,,,,,DOID:0060173,Timothy syndrome,C1832916,C536962,601005,MONDO:0010979,Timothy syndrome,Timothy syndrome (disorder) | Timothy syndrome | Long QT syndrome type 8
+BMGC_DS09912,BMG_DS037712,,"Portal Vein, Cavernous Transformation Of",,,,,,,C1832917,C563407,601004,MONDO:0010978,"portal vein, cavernous transformation of",
+BMGC_DS09913,BMG_DS037713,703530005,Brody myopathy,,,,,DOID:0050692,Brody myopathy,C1832918,C536607,601003,MONDO:0010977,Brody myopathy,Brody myopathy | Brody disease | Brody myopathy (disorder)
+BMGC_DS09914,BMG_DS037714,,"Epidermolysis Bullosa Simplex, Autosomal Recessive",,,,,,,C1832926,C563408,,,,
+BMGC_DS09915,BMG_DS037715,,"Deafness, Autosomal Dominant 5",,,,,,,C1832932,C563410,600994,MONDO:0010973,autosomal dominant nonsyndromic hearing loss 5,
+BMGC_DS09916,BMG_DS037716,,JUVENILE POLYPOSIS OF STOMACH,,,,,,,C1832940,,174900;600993,,,
+BMGC_DS09917,BMG_DS037717,,Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia,,,,,,,C1832942,C563412,175050,MONDO:0008278,juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome,
+BMGC_DS09918,BMG_DS037719,725905005,Infundibulopelvic dysgenesis,,,,,,,C1832949,C535528,MTHU054184;600989,MONDO:0010971,infundibulopelvic stenosis-multicystic kidney syndrome,Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | Infundibulopelvic stenosis multicystic kidney syndrome | Infundibulopelvic dysgenesis
+BMGC_DS09919,BMG_DS037720,,"Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies",,,,,DOID:0111697,"cleft palate, cardiac defects, and intellectual disabillity",C1832950,C563414,600987,MONDO:0010970,"cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies",
+BMGC_DS09920,BMG_DS037721,,Cone-Rod Dystrophy 5,,,,,DOID:0111010,cone-rod dystrophy 5,C1832976,C563415,600977,MONDO:0010969,cone-rod dystrophy 5,
+BMGC_DS09921,BMG_DS037722,,"GLAUCOMA 3, PRIMARY INFANTILE, B",,,,,,,C1832977,,600975,MONDO:0010968,"glaucoma 3, primary infantile, B",
+BMGC_DS09922,BMG_DS037723,,"Deafness, Autosomal Recessive 7",,,,,,,C1832978,C563417,600974,MONDO:0010967,autosomal recessive nonsyndromic hearing loss 7,
+BMGC_DS09923,BMG_DS037724,,"DEAFNESS, AUTOSOMAL RECESSIVE 6",,,,,,,C1832992,,607237;600971,MONDO:0010965,autosomal recessive nonsyndromic hearing loss 6,
+BMGC_DS09924,BMG_DS037725,,"EPIPHYSEAL DYSPLASIA, MULTIPLE, 3",,,,,DOID:0070304,multiple epiphyseal dysplasia 3,C1832998,,120270;600969,MONDO:0010964,"epiphyseal dysplasia, multiple, 3",
+BMGC_DS09925,BMG_DS037726,,"DEAFNESS, AUTOSOMAL DOMINANT 6",,,,,,,C1833021,,606201;600965,MONDO:0010963,autosomal dominant nonsyndromic hearing loss 6,
+BMGC_DS09926,BMG_DS037728,,"PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC",,,,,DOID:0050428,nonepidermolytic palmoplantar keratoderma,C1833030,,139350;600962,MONDO:0010962,diffuse nonepidermolytic palmoplantar keratoderma,
+BMGC_DS09927,BMG_DS037729,,Proprotein Convertase 1 3 Deficiency,,,,,DOID:0111698,proprotein convertase 1/3 deficiency,C1833053,C563423,600955,MONDO:0010961,obesity due to prohormone convertase I deficiency,
+BMGC_DS09928,BMG_DS037730,,,,,,,,,C1833104,,,MONDO:0100164,permanent neonatal diabetes mellitus,
+BMGC_DS09929,BMG_DS037732,,,,,,,,,C1833118,,,MONDO:0011430,pulverulent cataract,
+BMGC_DS09930,BMG_DS037733,719845008,Marden Walker like syndrome,,,,,DOID:0111699,Van den Ende-Gupta syndrome,C1833136,C535909,600920,MONDO:0010959,van den Ende-Gupta syndrome,Van den Ende-Gupta syndrome (disorder) | Van den Ende-Gupta syndrome | Marden Walker like syndrome
+BMGC_DS09931,BMG_DS037734,,Long Qt Syndrome 4,,,,,DOID:0111701,long QT syndrome 4,C1833154,C563428,,MONDO:0800323,long QT syndrome 4,
+BMGC_DS09932,BMG_DS037738,,"Hyperferritinemia, hereditary, with congenital cataracts",,,,,DOID:0111256,hyperferritinemia-cataract syndrome,C1833213,C538137,600886,MONDO:0010952,hereditary hyperferritinemia with congenital cataracts,
+BMGC_DS09933,BMG_DS037740,,"Charcot-Marie-Tooth disease, Type 2B",,,,,DOID:0110159,Charcot-Marie-Tooth disease type 2B,C1833219,C537989,600882,MONDO:0010949,Charcot-Marie-Tooth disease type 2B,
+BMGC_DS09934,BMG_DS037741,,"Cataract, Congenital Zonular, with Sutural Opacities",,,,,,,C1833229,C563435,600881,MONDO:0010948,cataract 10 multiple types,
+BMGC_DS09935,BMG_DS037742,,"Cardiomyopathy, Familial Hypertrophic, 6",,,,,,,C1833236,C563436,600858,MONDO:0010946,hypertrophic cardiomyopathy 6,
+BMGC_DS09936,BMG_DS037743,,Retinitis Pigmentosa 17,,,,,DOID:0110404,retinitis pigmentosa 17,C1833245,C563437,600852,MONDO:0010945,retinitis pigmentosa 17,
+BMGC_DS09937,BMG_DS037745,,SCHIZOPHRENIA 4,,,,,DOID:0070080,schizophrenia 4,C1833247,,600850,MONDO:0010943,schizophrenia 4,
+BMGC_DS09938,BMG_DS037746,,"Enuresis, Nocturnal, 2",,,,,,,C1833268,C563439,600808,MONDO:0010941,"nocturnal enuresis, 2",
+BMGC_DS09939,BMG_DS037747,,"Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative",,,,,,,C1833275,C563440,600802,MONDO:0010938,T-B+ severe combined immunodeficiency due to JAK3 deficiency,
+BMGC_DS09940,BMG_DS037749,,"FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED",,,,,,,C1833296,,600795;600795;614696,MONDO:0010936,frontotemporal dementia and/or amyotrophic lateral sclerosis 7,
+BMGC_DS09941,BMG_DS037750,,,,,,,DOID:0111203,autosomal dominant distal hereditary motor neuronopathy 5,C1833308,,,MONDO:0100350,"neuronopathy, distal hereditary motor, type 5",
+BMGC_DS09942,BMG_DS037751,,"Deafness, Autosomal Recessive 5",,,,,,,C1833319,C563444,600792,MONDO:0000912,autosomal recessive nonsyndromic hearing loss 5,
+BMGC_DS09943,BMG_DS037752,,"CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL",,,,,,,C1833321,,600790;616842,MONDO:0010932,progressive bifocal chorioretinal atrophy,
+BMGC_DS09944,BMG_DS037753,720496006,Anophthalmia plus syndrome,,,,,,,C1833339,C537767,600776,MONDO:0010930,anophthalmia plus syndrome,Anophthalmia plus syndrome (disorder) | Anophthalmia plus syndrome | Fryns microphthalmia syndrome
+BMGC_DS09945,BMG_DS037754,,Synostotic Posterior Plagiocephaly,Craniosynostoses,,,,,,C1833340,D003398,600775,MONDO:0010929,craniosynostosis 4,
+BMGC_DS09946,BMG_DS037756,,OROFACIAL CLEFT 3,,,,,,,C1833369,,600757,MONDO:0010927,orofacial cleft 3,
+BMGC_DS09947,BMG_DS037757,,"HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III",,,,,,,C1833372,,602242;600740,MONDO:0010926,familial hypocalciuric hypercalcemia 3,
+BMGC_DS09948,BMG_DS037758,,"Inclusion Body Myopathy, Autosomal Recessive",,,,,DOID:0080718,GNE myopathy,C1833373,C538329,,,,
+BMGC_DS09949,BMG_DS037760,,"Maturity-Onset Diabetes of the Young, Type 4",,,,,DOID:0111103,maturity-onset diabetes of the young type 4,C1833382,C563451,606392,MONDO:0011667,maturity-onset diabetes of the young type 4,
+BMGC_DS09950,BMG_DS037761,237960000,D-2-hydroxyglutaric aciduria,,,,,DOID:0050573,2-hydroxyglutaric aciduria,C1833429,C535306,MTHU006365,MONDO:0010924,D-2-hydroxyglutaric aciduria,D-2(OH) glutaric aciduria | D-2-hydroxyglutaric aciduria (disorder) | D-2-hydroxyglutaric aciduria
+BMGC_DS09951,BMG_DS037762,,Proximal Myopathy with Focal Depletion of Mitochondria,,,,,,,C1833453,C563453,600706,MONDO:0010923,proximal myopathy with focal depletion of mitochondria,
+BMGC_DS09952,BMG_DS037763,763630007,Satoyoshi syndrome,,,,,,,C1833454,C536616,600705,MONDO:0010922,Satoyoshi syndrome,Satoyoshi syndrome | Komuragaeri disease | Satoyoshi syndrome (disorder)
+BMGC_DS09953,BMG_DS037765,,"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5",,,,,DOID:0070272,hereditary nonpolyposis colorectal cancer type 5,C1833477,,614350,MONDO:0013710,Lynch syndrome 5,
+BMGC_DS09954,BMG_DS037766,,Microtia-Anotia,,,,,,,C1833486,C563457,600674,MONDO:0010920,microtia,
+BMGC_DS09955,BMG_DS037767,,"Varicella, Severe Recurrent",,,,,,,C1833487,C563458,600670,MONDO:0010919,"varicella, severe recurrent",
+BMGC_DS09956,BMG_DS037768,,Chondrocalcinosis 1,,,,,,,C1833499,C535938,600668,MONDO:0010917,chondrocalcinosis 1,
+BMGC_DS09957,BMG_DS037769,,"Deafness, Autosomal Dominant 4",,,,,,,C1833503,C563460,600652,MONDO:0010915,autosomal dominant nonsyndromic hearing loss 4A,
+BMGC_DS09958,BMG_DS037770,,,,,,,,,C1833508,,255110,MONDO:0009704,"carnitine palmitoyl transferase II deficiency, myopathic form",
+BMGC_DS09959,BMG_DS037771,,"CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE",,,,,,,C1833511,,600649;600650,MONDO:0010914,"carnitine palmitoyl transferase II deficiency, severe infantile form",
+BMGC_DS09960,BMG_DS037772,,"CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL",,,,,,,C1833518,,600650;608836,MONDO:0012136,"carnitine palmitoyl transferase II deficiency, neonatal form",
+BMGC_DS09961,BMG_DS037773,,OROFACIAL CLEFT 7,,,,,DOID:0060773,cleft lip-palate-ectodermal dysplasia syndrome,C1833538,,225060;600644,MONDO:0700251,orofacial cleft 7,
+BMGC_DS09962,BMG_DS037775,,UV-Sensitive Syndrome,,,,,DOID:0060240,UV-sensitive syndrome,C1833561,C563466,,MONDO:0015797,UV-sensitive syndrome,
+BMGC_DS09963,BMG_DS037777,,Cone-Rod Dystrophy 1,,,,,DOID:0111009,cone-rod dystrophy 1,C1833564,C563469,600624,MONDO:0010905,cone-rod dystrophy 1,
+BMGC_DS09964,BMG_DS037779,,"Craniosynostosis, Adelaide Type",,,,,,,C1833578,C563471,600593,MONDO:0010903,"craniosynostosis, Adelaide type",
+BMGC_DS09965,BMG_DS037780,,Spondyloepiphyseal Dysplasia with Atlantoaxial Instability,,,,,,,C1833603,C563472,600561,MONDO:0010902,"spondyloepiphyseal dysplasia, Reardon type",
+BMGC_DS09966,BMG_DS037781,,"Hydrocephalus, endocardial fibroelastosis, and cataracts",,,,,,,C1833607,C535855,600559,MONDO:0010901,HEC syndrome,
+BMGC_DS09967,BMG_DS037782,,PAROXYSMAL EXTREME PAIN DISORDER,,,,,DOID:0111537,paroxysmal extreme pain disorder,C1833661,,603415;167400,MONDO:0008179,paroxysmal extreme pain disorder,
+BMGC_DS09968,BMG_DS037783,,,,,,,,,C1833662,,,MONDO:0000507,inclusion body myopathy with Paget disease of bone and frontotemporal dementia,
+BMGC_DS09969,BMG_DS037784,722127006,Pacman dysplasia,,,,,,,C1833676,C538095,167220,MONDO:0008175,pacman dysplasia,Pacman dysplasia (disorder) | Pacman dysplasia | Epiphyseal stippling with osteoclastic hyperplasia syndrome
+BMGC_DS09970,BMG_DS037785,,,,,,,,,C1833683,,,MONDO:0957318,"nephrolithiasis, calcium oxalate",
+BMGC_DS09971,BMG_DS037786,,"Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension",,,,,,,C1833688,C563478,166990,MONDO:0008169,"osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension",
+BMGC_DS09972,BMG_DS037787,,"Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis",,,,,,,C1833689,C563479,166910,MONDO:0008166,"ovalocytosis, hereditary hemolytic, with defective erythropoiesis",
+BMGC_DS09973,BMG_DS037789,,Otofaciocervical Syndrome,,,,,,,C1833691,C563481,,MONDO:0008163,otofaciocervical syndrome,
+BMGC_DS09974,BMG_DS037790,,,,,,,,,C1833692,,166760,MONDO:0008162,"otitis media, susceptibility to",
+BMGC_DS09975,BMG_DS037791,,Otodental Dysplasia,,,,,,,C1833693,C563482,166750,MONDO:0008161,otodental syndrome,
+BMGC_DS09976,BMG_DS037792,,Osteosclerosis with Ichthyosis and Fractures,,,,,,,C1833697,C563483,166740,MONDO:0008160,osteosclerosis with ichthyosis and fractures,
+BMGC_DS09977,BMG_DS037793,,Osteopoikilosis and dacryocystitis,,,,,,,C1833698,C536061,166705,MONDO:0008158,dacryocystitis-osteopoikilosis syndrome,
+BMGC_DS09978,BMG_DS037794,,"Osteopoikilosis, Isolated",,,,,,,C1833699,C563484,,MONDO:0015634,isolated osteopoikilosis,
+BMGC_DS09979,BMG_DS037797,,Osteomas Of Mandible,,,,,,,C1833733,C563485,166400,MONDO:0008154,osteomas of mandible,
+BMGC_DS09980,BMG_DS037798,,"Osteogenesis imperfecta, Levin type",,,,,DOID:0111533,gnathodiaphyseal dysplasia,C1833736,C536039,166260,MONDO:0008151,gnathodiaphyseal dysplasia,
+BMGC_DS09981,BMG_DS037800,,"Ossicular Malformations, familial",,,,,,,C1833790,C537142,165680,MONDO:0008141,"ossicular malformations, familial",
+BMGC_DS09982,BMG_DS037801,,Ossified Ear Cartilages,,,,,,,C1833791,C563488,165670,MONDO:0008140,ossified ear cartilages,
+BMGC_DS09983,BMG_DS037802,,Oslam syndrome,,,,,,,C1833792,C537138,165660,MONDO:0008139,OSLAM syndrome,
+BMGC_DS09984,BMG_DS037803,,"Orbital Margin, Hypoplasia of",,,,,,,C1833795,C563490,165600,MONDO:0008138,syndromic orbital border hypoplasia,
+BMGC_DS09985,BMG_DS037804,,Orofaciodigital Syndrome X,,,,,DOID:0060380,orofaciodigital syndrome X,C1833796,C563491,165590,MONDO:0008137,orofaciodigital syndrome X,
+BMGC_DS09986,BMG_DS037805,,"Optic Nerve Hypoplasia, Bilateral",,,,,,,C1833797,C563492,165550,MONDO:0008136,isolated optic nerve hypoplasia,
+BMGC_DS09987,BMG_DS037806,,"Optic Nerve Aplasia, Bilateral",,,,,,,C1833798,C563493,,,,
+BMGC_DS09988,BMG_DS037808,,"OPTIC ATROPHY AND CATARACT, AUTOSOMAL DOMINANT",,,,,DOID:0111433,optic atrophy 3,C1833809,,606580;165300,MONDO:0008133,optic atrophy 3,
+BMGC_DS09989,BMG_DS037810,,"Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant",,,,,,,C1833831,C563497,165199,MONDO:0008131,"optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant",
+BMGC_DS09990,BMG_DS037811,,"Ophthalmoplegia, Progressive, with Scrotal Tongue and Mental Deficiency",,,,,,,C1833835,C563498,165150,MONDO:0008130,ophthalmoplegia-intellectual disability-lingua scrotalis syndrome,
+BMGC_DS09991,BMG_DS037812,,"Ophthalmoplegia, Familial Total, with Iris Transillumination",,,,,,,C1833836,C563499,165098,MONDO:0008129,"ophthalmoplegia, familial total, with iris transillumination",
+BMGC_DS09992,BMG_DS037813,,"Ophthalmoplegia, Familial Static",,,,,,,C1833839,C563500,165000,MONDO:0008128,"ophthalmoplegia, familial static",
+BMGC_DS09993,BMG_DS037814,,Ophthalmomandibulomelic Dysplasia,,,,,,,C1833872,C563501,164900,MONDO:0008127,ophthalmomandibulomelic dysplasia,
+BMGC_DS09994,BMG_DS037815,,"Onycholysis, Partial, with Scleronychia",,,,,,,C1833909,C563503,164800,MONDO:0008125,nonsyndromic congenital nail disorder 5,
+BMGC_DS09995,BMG_DS037816,,,,,,,,,C1833921,,155240,MONDO:0007958,familial medullary thyroid carcinoma,
+BMGC_DS09996,BMG_DS037820,,Oculopharyngodistal Myopathy,,,,,,,C1834014,C563508,,MONDO:0025193,oculopharyngodistal myopathy,
+BMGC_DS09997,BMG_DS037821,,,,,,,,,C1834038,,164220,MONDO:0008113,Schilbach-Rott syndrome,
+BMGC_DS09998,BMG_DS037823,,Hereditary vertical nystagmus,,,,,,,C1834078,C537857,164150,MONDO:0008107,"nystagmus, hereditary vertical",
+BMGC_DS09999,BMG_DS037824,,"Nystagmus 2, congenital, autosomal dominant",,,,,,,C1834079,C537854,164100,MONDO:0008106,"nystagmus 2, congenital, autosomal dominant",
+BMGC_DS10000,BMG_DS037826,,Noonan like syndrome,,,,,,,C1834120,C537846,,,,
+BMGC_DS10001,BMG_DS037827,,"Noduli Cutanei, Multiple, with Urinary Tract Abnormalities",,,,,,,C1834143,C563512,163850,MONDO:0008103,"noduli Cutanei, multiple, with urinary tract abnormalities",
+BMGC_DS10002,BMG_DS037828,,"Sick Sinus Syndrome 2, Autosomal Dominant",,,,,,,C1834144,C563513,163800,MONDO:0008102,"sick sinus syndrome 2, autosomal dominant",
+BMGC_DS10003,BMG_DS037829,,Hypertension Resistant to Conventional Therapy,,,,,,,C1834155,C563514,,,,
+BMGC_DS10004,BMG_DS037832,,"Neuropathy, congenital, with arthrogryposis multiplex",,,,,,,C1834206,C535714,162370,MONDO:0008084,"neuropathy, congenital, with arthrogryposis multiplex",
+BMGC_DS10005,BMG_DS037833,,"Ceroid Lipofuscinosis, Neuronal, Parry Type",Neuronal Ceroid-Lipofuscinoses,,,,,,C1834207,D009472,162350,MONDO:0008083,"ceroid lipofuscinosis, neuronal, 4 (Kufs type)",
+BMGC_DS10006,BMG_DS037837,,"NEUROFIBROMATOSIS, FAMILIAL SPINAL",,,,,DOID:0070482,spinal neurofibromatosis,C1834235,,162210;613113,MONDO:0008078,"neurofibromatosis, familial spinal",
+BMGC_DS10007,BMG_DS037838,,"AMYOTROPHY, HEREDITARY NEURALGIC",,,,,,,C1834304,,162100;604061,MONDO:0008076,amyotrophic neuralgia,
+BMGC_DS10008,BMG_DS037839,,RETINITIS PIGMENTOSA 27,,,,,,,C1834329,,162080;613750,MONDO:0013402,retinitis pigmentosa 27,
+BMGC_DS10009,BMG_DS037840,,"Retinal Degeneration, Autosomal Recessive, Clumped Pigment Type",,,,,,,C1834330,C563527,,,,
+BMGC_DS10010,BMG_DS037841,,,,,,,DOID:0060239,Van der Woude syndrome,C1834339,,,,,
+BMGC_DS10011,BMG_DS037842,,"Necrotizing Encephalomyelopathy, Subacute, of Leigh, Adult",,,,,,,C1834340,C563530,161700,MONDO:0008069,"necrotizing encephalomyelopathy, subacute, of Leigh, adult",
+BMGC_DS10012,BMG_DS037843,,"NASAL HYPERPIGMENTATION, FAMILIAL TRANSVERSE",,,,,,,C1834369,,161530,MONDO:0008066,"nasal hyperpigmentation, familial transverse",
+BMGC_DS10013,BMG_DS037844,,"NASAL GROOVE, FAMILIAL TRANSVERSE",,,,,,,C1834370,,161500,MONDO:0008065,"nasal groove, familial transverse",
+BMGC_DS10014,BMG_DS037845,,"Nasal Alar Collapse, Bilateral",,,,,,,C1834371,C563533,161470,MONDO:0008063,"nasal alar collapse, bilateral",
+BMGC_DS10015,BMG_DS037846,,Narcolepsy 1,,,,,,,C1834372,C563534,161400,MONDO:0008062,narcolepsy 1,
+BMGC_DS10016,BMG_DS037850,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10",,,,,DOID:0110316,hypertrophic cardiomyopathy 10,C1834460,,608758;160781,MONDO:0012112,hypertrophic cardiomyopathy 10,
+BMGC_DS10017,BMG_DS037851,,"CARDIOMYOPATHY, DILATED, 1S",,,,,,,C1834481,,613426;160760,MONDO:0013262,dilated cardiomyopathy 1S,
+BMGC_DS10018,BMG_DS037852,,,,,,,,,C1834523,,,MONDO:0011128,Sheldon-hall syndrome,
+BMGC_DS10019,BMG_DS037853,,Myopia 2,,,,,,,C1834531,C563541,160700,MONDO:0008053,"myopia 2, autosomal dominant",
+BMGC_DS10020,BMG_DS037854,,Myopathy with Storage of Glycoproteins and Glycosaminoglycans,,,,,,,C1834532,C563542,160570,MONDO:0008052,myopathy with storage of glycoproteins and Glycosaminoglycans,
+BMGC_DS10021,BMG_DS037856,,"Myopathy, Centronuclear, Autosomal Dominant","Myopathies, Structural, Congenital",,,,DOID:0111217,autosomal dominant centronuclear myopathy,C1834558,D020914,,,,
+BMGC_DS10022,BMG_DS037857,,"Continuous Muscle Fiber Activity, Hereditary",,,,,,,C1834559,C563545,,MONDO:0019943,hereditary continuous muscle fiber activity,
+BMGC_DS10023,BMG_DS037858,,"Myoglobinuria, Autosomal Dominant",,,,,,,C1834567,C563546,160010,MONDO:0008046,autosomal dominant myoglobinuria,
+BMGC_DS10024,BMG_DS037859,,Jankovic Rivera syndrome,,,,,DOID:0111527,spinal muscular atrophy with progressive myoclonic epilepsy,C1834569,C537563,159950,MONDO:0008045,spinal muscular atrophy-progressive myoclonic epilepsy syndrome,
+BMGC_DS10025,BMG_DS037860,439732004,Myoclonic dystonia,,,,,DOID:0090033,myoclonic dystonia,C1834570,C536096,159900,MONDO:0008044;MONDO:0000903,myoclonus-dystonia syndrome | myoclonic dystonia 11,Myoclonic dystonia (disorder) | Myoclonic dystonia
+BMGC_DS10026,BMG_DS037861,,"Myoclonus, Cerebellar Ataxia, and Deafness",,,,,,,C1834579,C563549,159800,MONDO:0008043,myoclonus-cerebellar ataxia-deafness syndrome,
+BMGC_DS10027,BMG_DS037863,,"Myoclonic Epilepsy, Hartung Type",,,,,,,C1834581,C563550,159600,MONDO:0008041,"myoclonic epilepsy, Hartung type",
+BMGC_DS10028,BMG_DS037864,,,,,,,,,C1834582,,159595,MONDO:0008040,transient myeloproliferative syndrome,
+BMGC_DS10029,BMG_DS037865,,,,,,,,,C1834600,,159500,MONDO:0008037,myelinated optic nerve fibers,
+BMGC_DS10030,BMG_DS037866,,"Myasthenia, Limb-Girdle, Autoimmune",,,,,,,C1834635,C563552,159400,MONDO:0008036,"myasthenia, limb-girdle, autoimmune",
+BMGC_DS10031,BMG_DS037868,,"Muscular Dystrophy, Pseudohypertrophic, With Internalized Capillaries",,,,,,,C1834652,C563554,159050,MONDO:0008034,"muscular dystrophy, pseudohypertrophic, with Internalized capillaries",
+BMGC_DS10032,BMG_DS037870,,"Muscular dystrophy, limb-girdle, type 1A",,,,,,,C1834659,C535906,,,,
+BMGC_DS10033,BMG_DS037871,,,,,,,,,C1834671,,158901,MONDO:0008031,facioscapulohumeral muscular dystrophy 2,
+BMGC_DS10034,BMG_DS037872,,Facioscapulohumeral muscular dystrophy 1a,,,,,,,C1834673,C536391,,,,
+BMGC_DS10035,BMG_DS037873,,BETHLEM MYOPATHY 1,,,,,,,C1834674,,158810,MONDO:0008029,Bethlem myopathy,
+BMGC_DS10036,BMG_DS037874,,"Muscular Dystrophy, Barnes Type",,,,,,,C1834688,C563558,158800,MONDO:0008028,"muscular dystrophy, Barnes type",
+BMGC_DS10037,BMG_DS037875,,"Muscular Atrophy, Malignant Neurogenic",,,,,,,C1834689,C563559,158650,MONDO:0008027,"muscular atrophy, malignant neurogenic",
+BMGC_DS10038,BMG_DS037876,,"Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant",,,,,,,C1834690,C563560,,MONDO:0018190,autosomal dominant childhood-onset proximal spinal muscular atrophy,
+BMGC_DS10039,BMG_DS037877,,,,,,,,,C1834692,,158590,MONDO:0008025,"neuronopathy, distal hereditary motor, type 2A",
+BMGC_DS10040,BMG_DS037878,,"Neuropathy, Distal Hereditary Motor, Type VIIA",,,,,,,C1834703,C563562,158580,MONDO:0008024,"neuronopathy, distal hereditary motor, type 7A",
+BMGC_DS10041,BMG_DS037879,,"Muscle Cramps, Familial",,,,,,,C1834708,C563563,158400,MONDO:0008022,"muscle cramps, familial",
+BMGC_DS10042,BMG_DS037880,,CEREBELLOPARENCHYMAL DISORDER VI,,,,,,,C1834711,,158350,,,
+BMGC_DS10043,BMG_DS037883,,Multiple Exostoses with Spastic Tetraparesis,,,,,,,C1834724,C563566,158345,MONDO:0008020,multiple exostoses with spastic tetraparesis,
+BMGC_DS10044,BMG_DS037884,,NONDISJUNCTION,,,,,,,C1834741,,158250,MONDO:0008014,nondisjunction,
+BMGC_DS10045,BMG_DS037885,,"CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV",,,,,,,C1834751,,158105,,,
+BMGC_DS10046,BMG_DS037886,,Monophalangy of Great Toe,,,,,,,C1834753,C563570,158100,MONDO:0008012,Monophalangy of great toe,
+BMGC_DS10047,BMG_DS037889,,Macrosomia obesity macrocephaly ocular abnormalities,,,,,,,C1834759,C535812,157980,MONDO:0008008,MOMO syndrome,
+BMGC_DS10048,BMG_DS037890,,MYXOMATOUS MITRAL VALVE PROLAPSE 1,,,,,,,C1834819,,157700,MONDO:0024529,MVP1,
+BMGC_DS10049,BMG_DS037891,,METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS,,,,,,,C1834821,,157660;250460,MONDO:0009601,metaphyseal dysplasia without hypotrichosis,
+BMGC_DS10050,BMG_DS037892,,"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1",,,,,,,C1834846,C563575,157640,MONDO:0024528,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1",
+BMGC_DS10051,BMG_DS037894,,,,,,,,,C1834870,,157600,MONDO:0008002,mirror movements 1,
+BMGC_DS10052,BMG_DS037896,,Holoprosencephaly 2,,,,,DOID:0110872,holoprosencephaly 2,C1834877,C563579,157170,MONDO:0007999,holoprosencephaly 2,
+BMGC_DS10053,BMG_DS037899,,"Microphthalmia, Isolated, With Corectopia",,,,,,,C1834918,C563581,156900,MONDO:0007996,"microphthalmia, isolated, with corectopia",
+BMGC_DS10054,BMG_DS037900,,"Microphthalmia, Isolated, with Cataract 1",,,,,,,C1834919,C563582,156850,MONDO:0007995,"microphthalmia, isolated, with cataract 1",
+BMGC_DS10055,BMG_DS037901,,Cloverleaf skull micromelia thoracic dysplasia,,,,,,,C1834928,C536429,156830,MONDO:0007994,micromelic bone dysplasia with cloverleaf skull,
+BMGC_DS10056,BMG_DS037903,,"Microcornea, glaucoma, and absent frontal sinuses",,,,,,,C1834935,C537552,156700,MONDO:0007992,microcornea-glaucoma-absent frontal sinuses syndrome,
+BMGC_DS10057,BMG_DS037904,,"Metatarsus Varus, Type I",,,,,,,C1834968,C563585,156520,MONDO:0007985,"metatarsus varus, type 1",
+BMGC_DS10058,BMG_DS037905,,Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly,,,,,,,C1834969,C563586,,,,
+BMGC_DS10059,BMG_DS037908,,"MESOMELIC DYSPLASIA, KANTAPUTRA TYPE",,,,,,,C1835009,,156232,MONDO:0007977,"mesomelic dysplasia, Kantaputra type",
+BMGC_DS10060,BMG_DS037910,,"Meralgia Paraesthetica, Familial",,,,,,,C1835026,C563590,156220,MONDO:0007975,"meralgia paraesthetica, familial",
+BMGC_DS10061,BMG_DS037911,,Mental and Growth Retardation with Amblyopia,,,,,,,C1835028,C563591,156190,MONDO:0007973,mental and growth retardation with amblyopia,
+BMGC_DS10062,BMG_DS037912,,"Membranous Cranial Ossification, Delayed",,,,,,,C1835030,C563592,155980,MONDO:0007971,delayed membranous cranial ossification,
+BMGC_DS10063,BMG_DS037915,,,,,,,DOID:0111511,melanoma and neural system tumor syndrome,C1835042,,155755,MONDO:0007967,melanoma and neural system tumor syndrome,
+BMGC_DS10064,BMG_DS037916,,,,,,,,,C1835043,,155700,MONDO:0007965,"melanoma, malignant familial intraocular",
+BMGC_DS10065,BMG_DS037917,,,,,,,,,C1835044,,155601,MONDO:0007964,"melanoma, cutaneous malignant, susceptibility to, 2",
+BMGC_DS10066,BMG_DS037918,,,,,,,,,C1835047,,155600,MONDO:0007963,"melanoma, cutaneous malignant, susceptibility to, 1",
+BMGC_DS10067,BMG_DS037920,,,,,,,,,C1835085,,155200,MONDO:0007957,mediosternal depigmentation line,
+BMGC_DS10068,BMG_DS037922,,"Median cleft lip, corpus callosum, lipoma, and skin polyps",,,,,,,C1835087,C536135,155145,MONDO:0007956,Pai syndrome,
+BMGC_DS10069,BMG_DS037923,,Maxillofacial Dysostosis,,,,,,,C1835088,C563599,155000,MONDO:0007952,maxillofacial dysostosis,
+BMGC_DS10070,BMG_DS037926,,"Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type",,,,,,,C1835134,C563601,154570,MONDO:0007945,"mannose 6-phosphate receptor recognition defect, Lebanese type",
+BMGC_DS10071,BMG_DS037927,,,,,,,,,C1835159,,154300,MONDO:0007941,malocclusion due to protuberant upper front teeth,
+BMGC_DS10072,BMG_DS037930,,"Hypomagnesemia 2, renal",,,,,,,C1835171,C537152,154020,MONDO:0007937,renal hypomagnesemia 2,
+BMGC_DS10073,BMG_DS037932,,"Macular Dystrophy, Fenestrated Sheen Type",,,,,,,C1835173,C563607,153890,MONDO:0007936,"macular dystrophy, fenestrated sheen type",
+BMGC_DS10074,BMG_DS037933,,"MACULAR DYSTROPHY, ATYPICAL VITELLIFORM",,,,,,,C1835178,,153840,,,
+BMGC_DS10075,BMG_DS037934,,"MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1",,,,,,,C1835192,,153600,MONDO:0100281,"macroglobulinemia, Waldenstrom, 1",
+BMGC_DS10076,BMG_DS037935,,,,,,,,,C1835223,,607507,MONDO:0100232,"psoriatic arthritis, susceptibility to",
+BMGC_DS10077,BMG_DS037936,,"Lymphedema, microcephaly and chorioretinopathy syndrome",,,,,DOID:0060349,"microcephaly with or without chorioretinopathy, lymphedema, or mental retardation",C1835265,C537711,152950,MONDO:0007918,"microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability",
+BMGC_DS10078,BMG_DS037937,,Lymphedema and Cerebral Arteriovenous Anomaly,,,,,,,C1835272,C563612,152900,MONDO:0007917,lymphedema-cerebral arteriovenous anomaly syndrome,
+BMGC_DS10079,BMG_DS037939,,"Lumbar Stenosis, Familial",,,,,,,C1835320,C563613,152550,MONDO:0007914,"lumbar stenosis, familial",
+BMGC_DS10080,BMG_DS037941,,,,,,,,,C1835356,,152420,MONDO:0007912,lithium transport,
+BMGC_DS10081,BMG_DS037945,,"Lp(A) Deficiency, Congenital",,,,,,,C1835362,C563618,,,,
+BMGC_DS10082,BMG_DS037947,,,,,,,,,C1835373,,151700,MONDO:0007907,lipoma of the conjunctiva,
+BMGC_DS10083,BMG_DS037948,,"Lip, Hamartomatous",,,,,,,C1835395,C563621,151640,MONDO:0007905,"lip, hamartomatous",
+BMGC_DS10084,BMG_DS037949,722034006,Median nodule of upper lip,,,,,,,C1835396,,151630,MONDO:0007904,median nodule of the upper lip,Median nodule of upper lip (disorder) | Median nodule of upper lip
+BMGC_DS10085,BMG_DS037950,,LI-FRAUMENI SYNDROME 1,,,,,,,C1835398,,191170,,,
+BMGC_DS10086,BMG_DS037951,,"Lichen Planus, Familial",,,,,,,C1835402,C563624,151620,MONDO:0007902,"lichen planus, familial",
+BMGC_DS10087,BMG_DS037952,,Levator-Medial Rectus Synkinesis,,,,,,,C1835403,C563625,151610,MONDO:0007901,levator-medial rectus synkinesis,
+BMGC_DS10088,BMG_DS037953,,"Leukocyte Nuclear Appendages, Hereditary Prevalence of",,,,,,,C1835405,C563626,151500,MONDO:0007898,"leukocyte nuclear appendages, hereditary prevalence of",
+BMGC_DS10089,BMG_DS037954,,,,,,,,,C1835407,,609532,MONDO:0012292,"hepatitis C virus, susceptibility to",
+BMGC_DS10090,BMG_DS037955,,"Platyspondylic Lethal Skeletal Dysplasia, Torrance Type",,,,,DOID:0111508,Torrance type platyspondylic dysplasia,C1835437,C563627,151210,MONDO:0007895,"platyspondylic dysplasia, Torrance type",
+BMGC_DS10091,BMG_DS037956,,Leri pleonosteosis,,,,,,,C1835450,C537118,151200,MONDO:0007894,Leri pleonosteosis,
+BMGC_DS10092,BMG_DS037957,,"Lentiginosis, Centrofacial Neurodysraphic",,,,,,,C1835484,C563630,151000,MONDO:0007890,"lentiginosis, centrofacial neurodysraphic",
+BMGC_DS10093,BMG_DS037958,,,,,,,,,C1835488,,150700,MONDO:0007887,leiomyoma of vulva and esophagus,
+BMGC_DS10094,BMG_DS037961,,"Tooth Agenesis, Selective, 4",,,,,,,C1835492,C563634,150400,MONDO:0007881,"tooth agenesis, selective, 4",
+BMGC_DS10095,BMG_DS037962,,"Succedaneous Teeth, Agenesis Of",,,,,,,C1835493,C563634,,,,
+BMGC_DS10096,BMG_DS037964,,"Lactic Acidosis, Chronic Adult Form",,,,,,,C1835591,C563640,150170,MONDO:0007873,"lactic acidosis, chronic adult form",
+BMGC_DS10097,BMG_DS037965,,,,,,,,,C1835612,,149700,MONDO:0007871,familial congenital nasolacrimal duct obstruction,
+BMGC_DS10098,BMG_DS037966,,,,,,,,,C1835613,,149600,MONDO:0007870,"labia minora, incomplete adhesion of",
+BMGC_DS10099,BMG_DS037967,,,,,,,,,C1835614,,,MONDO:0021022,hereditary hyperekplexia,
+BMGC_DS10100,BMG_DS037968,,Keratosis focal palmoplantar gingival,,,,,DOID:0070553,focal palmoplantar and gingival keratosis,C1835650,C536157,148730,MONDO:0007860,focal palmoplantar and gingival keratoderma,
+BMGC_DS10101,BMG_DS037969,,Keratosis palmoplantaris papulosa,,,,,,,C1835662,C536161,,MONDO:0019332,punctate palmoplantar keratoderma type 1,
+BMGC_DS10102,BMG_DS037970,,Keratosis Palmaris et Plantaris with Clinodactyly,,,,,,,C1835663,C563646,148520,MONDO:0007857,keratosis palmaris et plantaris-clinodactyly syndrome,
+BMGC_DS10103,BMG_DS037971,,,,,,,DOID:0111506,palmoplantar keratoderma-esophageal carcinoma syndrome,C1835664,,148500,MONDO:0007856,palmoplantar keratoderma-esophageal carcinoma syndrome,
+BMGC_DS10104,BMG_DS037972,,Keratoderma palmoplantar spastic paralysis,,,,,,,C1835671,C536153,148360,MONDO:0007853,palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome,
+BMGC_DS10105,BMG_DS037973,,Palmoplantar Keratoderma with Deafness,,,,,DOID:0111505,palmoplantar keratoderma-deafness syndrome,C1835672,C536152,148350,MONDO:0007852,palmoplantar keratoderma-deafness syndrome,
+BMGC_DS10106,BMG_DS037974,,Keratoconus 1,,,,,,,C1835677,C563649,148300,MONDO:0007851,keratoconus 1,
+BMGC_DS10107,BMG_DS037975,,Keratitis Fugax Hereditaria,,,,,,,C1835697,C563650,148200,MONDO:0007849,keratitis fugax hereditaria,
+BMGC_DS10108,BMG_DS037976,,"Keratitis, hereditary",,,,,DOID:0111383,autosomal dominant keratitis,C1835698,C537022,148190,MONDO:0007848,autosomal dominant keratitis,
+BMGC_DS10109,BMG_DS037977,,,,,,,,,C1835713,,,MONDO:0800422,"cirrhosis, noncryptogenic, susceptibility to",
+BMGC_DS10110,BMG_DS037980,,,,,,,,,C1835808,,615953,MONDO:0014415,"kallikrein, decreased urinary activity of",
+BMGC_DS10111,BMG_DS037981,,Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency,,,,,,,C1835813,C563654,610842,MONDO:0012570,body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency,
+BMGC_DS10112,BMG_DS037982,,"Mitral Valve Prolapse, Myxomatous 3",,,,,,,C1835814,C563655,610840,MONDO:0012569,"mitral valve prolapse, myxomatous 3",
+BMGC_DS10113,BMG_DS037984,,"FANCONI ANEMIA, COMPLEMENTATION GROUP N",,,,,DOID:0111094,Fanconi anemia complementation group N,C1835817,,610355;610832,MONDO:0012565,Fanconi anemia complementation group N,
+BMGC_DS10114,BMG_DS037986,,Holoprosencephaly 9,,,,,DOID:0110873,holoprosencephaly 9,C1835819,C563659,610829,MONDO:0012563,holoprosencephaly 9,
+BMGC_DS10115,BMG_DS037987,,HOLOPROSENCEPHALY 7,,,,,,,C1835820,,601309;610828,MONDO:0012562,holoprosencephaly 7,
+BMGC_DS10116,BMG_DS037988,,,,,,,,,C1835826,,610805,MONDO:0012561,congenital anomalies of kidney and urinary tract 1,
+BMGC_DS10117,BMG_DS037989,,Immunodeficiency due to Defect in MAPBP-Interacting Protein,,,,,,,C1835829,C563663,610798,MONDO:0012559,primary immunodeficiency syndrome due to p14 deficiency,
+BMGC_DS10118,BMG_DS037990,,"Epiphyseal Dysplasia, Baumann Type",,,,,,,C1835830,C563664,610797,MONDO:0012558,"epiphyseal dysplasia, Baumann type",
+BMGC_DS10119,BMG_DS037991,,Mitochondrial Phosphate Carrier Deficiency,,,,,,,C1835845,C563665,610773,MONDO:0012557,cardiomyopathy-hypotonia-lactic acidosis syndrome,
+BMGC_DS10120,BMG_DS037992,,"Congenital Disorder Of Glycosylation, Type Im",,,,,,,C1835849,C563666,610768,MONDO:0012556,DK1-congenital disorder of glycosylation,
+BMGC_DS10121,BMG_DS037993,,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11",,,,,,,C1835851,,602400;606797,MONDO:0011218,autosomal recessive congenital ichthyosis 11,
+BMGC_DS10122,BMG_DS037994,,Alopecia-Mental Retardation Syndrome 2,,,,,DOID:0080629,alopecia-mental retardation syndrome 2,C1835852,C563668,610422,MONDO:0012487,alopecia-intellectual disability syndrome 2,
+BMGC_DS10123,BMG_DS037995,,"DEAFNESS, AUTOSOMAL RECESSIVE 68",,,,,,,C1835854,,605111;610419,MONDO:0012485,autosomal recessive nonsyndromic hearing loss 68,
+BMGC_DS10124,BMG_DS037997,,Cone-Rod Dystrophy 11,,,,,DOID:0111018,cone-rod dystrophy 11,C1835865,C563671,610381,MONDO:0012483,cone-rod dystrophy 11,
+BMGC_DS10125,BMG_DS037998,,,,,,,,,C1835867,,610379,MONDO:0012482,"West Nile virus, susceptibility to",
+BMGC_DS10126,BMG_DS038000,,"Diabetes Mellitus, Transient Neonatal, 2",,,,,,,C1835887,C563672,610374,MONDO:0012480,"diabetes mellitus, transient neonatal, 2",
+BMGC_DS10127,BMG_DS038001,,"Diarrhea 4, Malabsorptive, Congenital",,,,,,,C1835888,C563673,610370,MONDO:0012479,congenital malabsorptive diarrhea 4,
+BMGC_DS10128,BMG_DS038002,,Orofacial Cleft 9,,,,,DOID:0080402,orofacial cleft 9,C1835894,C563675,610361,MONDO:0012478,orofacial cleft 9,
+BMGC_DS10129,BMG_DS038003,,Retinitis Pigmentosa 33,,,,,DOID:0110366,retinitis pigmentosa 33,C1835895,C563676,610359,MONDO:0012477,retinitis pigmentosa 33,
+BMGC_DS10130,BMG_DS038004,,"Spastic Paraplegia 30, Autosomal Recessive",,,,,,,C1835896,C563677,,,,
+BMGC_DS10131,BMG_DS038005,,Retinal Cone Dystrophy 3B,,,,,DOID:0081022,retinal cone dystrophy 3B,C1835897,C563678,610356,MONDO:0012475,cone dystrophy with supernormal rod response,
+BMGC_DS10132,BMG_DS038006,,"Epilepsy, Nocturnal Frontal Lobe, Type 4",,,,,,,C1835905,C563679,610353,MONDO:0012474,autosomal dominant nocturnal frontal lobe epilepsy 4,
+BMGC_DS10133,BMG_DS038007,,Familial anomalous origin of right pulmonary artery,,,,,,,C1835910,C535681,610338,MONDO:0012473,"right pulmonary artery, anomalous origin of, familial",
+BMGC_DS10134,BMG_DS038008,,AICARDI-GOUTIERES SYNDROME 4,,,,,,,C1835912,,606034;610333,MONDO:0012472,Aicardi-Goutieres syndrome 4,
+BMGC_DS10135,BMG_DS038010,,AICARDI-GOUTIERES SYNDROME 3,,,,,,,C1835916,,610329;610330,MONDO:0012471,Aicardi-Goutieres syndrome 3,
+BMGC_DS10136,BMG_DS038011,,,,,,,,,C1835919,,609939,MONDO:0012369,"systemic lupus erythematosus, susceptibility to, 6",
+BMGC_DS10137,BMG_DS038012,709282004,Aminoacylase 1 deficiency,,,,,,,C1835922,C538246,609924,MONDO:0012368,aminoacylase 1 deficiency,Aminoacylase 1 deficiency | Deficiency of aminoacylase 1 (disorder) | Deficiency of aminoacylase 1
+BMGC_DS10138,BMG_DS038013,,Retinitis Pigmentosa 31,,,,,DOID:0110391,retinitis pigmentosa 31,C1835923,C563685,609923,MONDO:0012367,retinitis pigmentosa 31,
+BMGC_DS10139,BMG_DS038016,,"Cardiomyopathy, Dilated, 1q",,,,,,,C1835926,C563688,609915,MONDO:0012364,dilated cardiomyopathy 1Q,
+BMGC_DS10140,BMG_DS038017,,Retinitis Pigmentosa 32,,,,,DOID:0110355,retinitis pigmentosa 32,C1835927,C563689,609913,MONDO:0012363,retinitis pigmentosa 32,
+BMGC_DS10141,BMG_DS038018,,"CARDIOMYOPATHY, DILATED, 1P",,,,,,,C1835928,,172405;609909,MONDO:0012362,dilated cardiomyopathy 1P,
+BMGC_DS10142,BMG_DS038020,,"ALPHA/BETA T-CELL LYMPHOPENIA WITH GAMMA/DELTA T-CELL EXPANSION, SEVERE CYTOMEGALOVIRUS INFECTION, AND AUTOIMMUNITY",,,,,,,C1835931,,179615;609889,MONDO:0012359,combined immunodeficiency due to partial RAG1 deficiency,
+BMGC_DS10143,BMG_DS038021,,,,,,,,,C1835932,,609888,MONDO:0012358,"leprosy, susceptibility to, 1",
+BMGC_DS10144,BMG_DS038022,,"Glaucoma 1, Open Angle, G",,,,,,,C1835933,C563692,609887,MONDO:0012357,"obsolete glaucoma 1, open angle, G",
+BMGC_DS10145,BMG_DS038027,,PARIETAL FORAMINA 3,,,,,,,C1835980,,609566,MONDO:0012302,parietal foramina 3,
+BMGC_DS10146,BMG_DS038029,,Nanophthalmos 2,,,,,,,C1836006,C563700,609549,MONDO:0012299,nanophthalmos 2,
+BMGC_DS10147,BMG_DS038031,,"Spastic Paraplegia, Optic Atrophy, and Neuropathy",,,,,DOID:0060491,SPOAN syndrome,C1836010,C563702,609541,MONDO:0012297,"spastic paraplegia, optic atropy, and neuropathy",
+BMGC_DS10148,BMG_DS038034,,"Drug Metabolism, Poor, CYP2C19-Related",,,,,,,C1836023,C563703,,,,
+BMGC_DS10149,BMG_DS038035,,"Deafness, Autosomal Recessive 23",,,,,,,C1836027,C563705,609533,MONDO:0012293,autosomal recessive nonsyndromic hearing loss 23,
+BMGC_DS10150,BMG_DS038036,,Immunoglobulin a deficiency 2,,,,,,,C1836032,C536291,609529,MONDO:0012291,immunoglobulin A deficiency 2,
+BMGC_DS10151,BMG_DS038037,,"Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome",,,,,DOID:0060337,CEDNIK syndrome,C1836033,C537943,609528,MONDO:0012290,CEDNIK syndrome,
+BMGC_DS10152,BMG_DS038038,,"Filaminopathy, autosomal dominant",,,,,,,C1836050,C537932,609524,MONDO:0012289,myofibrillar myopathy 5,
+BMGC_DS10153,BMG_DS038040,,"Stickler Syndrome, Type I, Nonsyndromic Ocular",,,,,,,C1836080,C563709,609508,MONDO:0012287,"Stickler syndrome, type I, nonsyndromic ocular",
+BMGC_DS10154,BMG_DS038041,,"RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT",,,,,,,C1836081,,120140;609508,MONDO:0016202,autosomal dominant rhegmatogenous retinal detachment,
+BMGC_DS10155,BMG_DS038042,,LEFT VENTRICULAR NONCOMPACTION 2,,,,,,,C1836118,,609470,MONDO:0012285,left ventricular noncompaction 2,
+BMGC_DS10156,BMG_DS038045,,Al-Gazali Syndrome,,,,,,,C1836121,C536817,609465,MONDO:0012282,Al-Gazali syndrome,
+BMGC_DS10157,BMG_DS038046,,"SARCOIDOSIS, EARLY-ONSET",,,,,,,C1836122,,186580,,,
+BMGC_DS10158,BMG_DS038047,,Goldberg-Shprintzen megacolon syndrome,,,,,DOID:0060481,Goldberg-Shprintzen syndrome,C1836123,C537279,609460,MONDO:0012280,Goldberg-Shprintzen syndrome,
+BMGC_DS10159,BMG_DS038049,,"Supranuclear Palsy, Progressive, 2",,,,,,,C1836148,C563717,609454,MONDO:0012278,"supranuclear palsy, progressive, 2",
+BMGC_DS10160,BMG_DS038050,,"Myopathy, Myofibrillar, Zasp-Related",,,,,,,C1836155,C563718,,,,
+BMGC_DS10161,BMG_DS038051,,Generalized Epilepsy and Paroxysmal Dyskinesia,,,,,,,C1836173,C563719,,,,
+BMGC_DS10162,BMG_DS038052,,"Chondrodysplasia, acromesomelic, with genital anomalies",,,,,,,C1836182,C537913,,,,
+BMGC_DS10163,BMG_DS038053,,"DEAFNESS, AUTOSOMAL RECESSIVE 48",,,,,,,C1836199,,605564;609439,MONDO:0012273,autosomal recessive nonsyndromic hearing loss 48,
+BMGC_DS10164,BMG_DS038054,,"Mental retardation, keratoconus, febrile seizures, and sinoatrial block",,,,,,,C1836202,C537452,609438,MONDO:0012272,"intellectual disability, keratoconus, febrile seizures, and sinoatrial block",
+BMGC_DS10165,BMG_DS038055,,"Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction",,,,,,,C1836206,C563721,609432,MONDO:0012271,mesoaxial synostotic syndactyly with phalangeal reduction,
+BMGC_DS10166,BMG_DS038056,,Tukel syndrome,,,,,DOID:0081021,Tukel syndrome,C1836217,C536925,609428,MONDO:0012270,Tukel syndrome,
+BMGC_DS10167,BMG_DS038057,,,,,,,,,C1836230,,609423,MONDO:0004951,susceptibility to HIV infection,
+BMGC_DS10168,BMG_DS038058,,Holoprosencephaly 8,,,,,DOID:0110879,holoprosencephaly 8,C1836254,C563723,609408,MONDO:0012267,holoprosencephaly 8,
+BMGC_DS10169,BMG_DS038059,,Preeclampsia Eclampsia 4,,,,,,,C1836255,C563724,609404,MONDO:0012266,preeclampsia/eclampsia 4,
+BMGC_DS10170,BMG_DS038064,,"Cataract, Congenital Nuclear, Autosomal Recessive 1",,,,,,,C1836272,C563728,609376,MONDO:0012260,cataract 35,
+BMGC_DS10171,BMG_DS038065,,Epidermolysis Bullosa Simplex with Migratory Circinate Erythema,,,,,,,C1836284,C563730,609352,MONDO:0012258,"epidermolysis bullosa simplex 2E, with migratory circinate erythema",
+BMGC_DS10172,BMG_DS038067,,"Spastic Paraplegia 28, Autosomal Recessive",,,,,,,C1836295,C563732,609340,MONDO:0012256,hereditary spastic paraplegia 28,
+BMGC_DS10173,BMG_DS038068,,Carotid Intimal Medial Thickness 1,,,,,,,C1836302,C563733,,,,
+BMGC_DS10174,BMG_DS038071,,,,,,,,,C1836315,,609324,MONDO:0012253,"multiple epiphyseal dysplasia, with severe proximal femoral dysplasia",
+BMGC_DS10175,BMG_DS038072,,Rhabdoid Tumor Predisposition Syndrome 1,,,,,,,C1836327,C563738,609322,MONDO:0012252,rhabdoid tumor predisposition syndrome 1,
+BMGC_DS10176,BMG_DS038073,,Erythrokeratodermia Variabilis 3,,,,,,,C1836330,C563739,609313,MONDO:0012251,MEDNIK syndrome,
+BMGC_DS10177,BMG_DS038074,,"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H",,,,,,,C1836336,,609311;611104,MONDO:0012250,Charcot-Marie-Tooth disease type 4H,
+BMGC_DS10178,BMG_DS038075,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K",,,,,,,C1836373,,609308,MONDO:0012248,autosomal recessive limb-girdle muscular dystrophy type 2K,
+BMGC_DS10179,BMG_DS038076,,SPINOCEREBELLAR ATAXIA 27,,,,,DOID:0050976,spinocerebellar ataxia type 27,C1836383,,193003;609307,MONDO:0012247,spinocerebellar ataxia type 27,
+BMGC_DS10180,BMG_DS038077,,SPINOCEREBELLAR ATAXIA 26,,,,,,,C1836395,,130610;609306,MONDO:0012246,spinocerebellar ataxia type 26,
+BMGC_DS10181,BMG_DS038079,,"B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations",,,,,,,C1836437,C563745,609296,MONDO:0012243,"B-cell immunodeficiency, distal limb anomalies, and urogenital malformations",
+BMGC_DS10182,BMG_DS038080,,Familial neurocardiogenic syncope,,,,,,,C1836438,C536849,609289,MONDO:0012242,"syncope, familial vasovagal",
+BMGC_DS10183,BMG_DS038081,,"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3",,,,,,,C1836439,C563747,609286,MONDO:0012241,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3",
+BMGC_DS10184,BMG_DS038082,,Nemaline myopathy 4,,,,,DOID:0110932,nemaline myopathy 4,C1836447,C538351,609285,MONDO:0012240,congenital myopathy 23,
+BMGC_DS10185,BMG_DS038083,,Nemaline myopathy 1,,,,,DOID:0110926,nemaline myopathy 1,C1836448,C538348,,,,
+BMGC_DS10186,BMG_DS038084,,"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2",,,,,,,C1836460,C563750,609283,MONDO:0012238,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2",
+BMGC_DS10187,BMG_DS038085,,Nemaline myopathy 6,,,,,DOID:0110935,nemaline myopathy 6,C1836472,C538398,609273,MONDO:0012237,nemaline myopathy 6,
+BMGC_DS10188,BMG_DS038087,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7",,,,,DOID:0080059,autosomal recessive spinocerebellar ataxia 7,C1836474,,609270;607998,MONDO:0012235,autosomal recessive spinocerebellar ataxia 7,
+BMGC_DS10189,BMG_DS038089,,Li-Fraumeni Syndrome 2,,,,,DOID:0111504,Li-Fraumeni syndrome 2,C1836482,C563755,609265,MONDO:0012233,obsolete Li-Fraumeni syndrome 2,
+BMGC_DS10190,BMG_DS038090,,"Stuttering, Familial Persistent 2",,,,,,,C1836484,C563756,609261,MONDO:0012232,"stuttering, familial persistent, 2",
+BMGC_DS10191,BMG_DS038091,,"Charcot-Marie-Tooth Disease, Axonal, Type 2A2",,,,,,,C1836485,C563757,,,,
+BMGC_DS10192,BMG_DS038092,,Myopia 10,,,,,,,C1836503,C563758,609259,MONDO:0012230,myopia 10,
+BMGC_DS10193,BMG_DS038093,,Myopia 9,,,,,,,C1836504,C563759,609258,MONDO:0012229,myopia 9,
+BMGC_DS10194,BMG_DS038094,,Myopia 8,,,,,,,C1836505,C563760,609257,MONDO:0012228,myopia 8,
+BMGC_DS10195,BMG_DS038095,,Myopia 7,,,,,,,C1836506,C563761,609256,MONDO:0012227,myopia 7,
+BMGC_DS10196,BMG_DS038096,,,,,,,,,C1836507,,609255,MONDO:0012226,"febrile seizures, familial, 5",
+BMGC_DS10197,BMG_DS038097,1208969008,Generalized onset tonic epileptic seizure,,,,,,,C1836508,,,,,Generalised tonic seizure | Generalized tonic seizure | Generalized onset tonic epileptic seizure (finding) | Generalized onset tonic epileptic seizure | Generalised onset tonic epileptic seizure | Generalized-onset tonic epileptic seizure | Generalised-onset tonic epileptic seizure
+BMGC_DS10198,BMG_DS038098,,Senior-Loken Syndrome 5,,,,,,,C1836517,C563763,609254,MONDO:0012225,Senior-Loken syndrome 5,
+BMGC_DS10199,BMG_DS038099,,,,,,,,,C1836518,,609253,MONDO:0012224,"febrile seizures, familial, 6",
+BMGC_DS10200,BMG_DS038101,880065001,Alpha-N-acetylgalactosaminidase deficiency type 2,,,,,,,C1836522,C536631,609242,MONDO:0012222,alpha-N-acetylgalactosaminidase deficiency type 2,Alpha-N-acetylgalactosaminidase deficiency type 2 | Alpha-N-acetylgalactosaminidase deficiency type 2 (disorder) | Schindler disease type 2 | NAGA (alpha-N-acetylgalactosaminidase) deficiency type 2
+BMGC_DS10201,BMG_DS038102,879937000,Alpha-N-acetylgalactosaminidase deficiency type 1,,,,,,,C1836544,,609241,MONDO:0012221,alpha-N-acetylgalactosaminidase deficiency type 1,Schindler disease type 1 | Alpha-N-acetylgalactosaminidase deficiency type 1 | Alpha-N-acetylgalactosaminidase deficiency type 1 (disorder) | NAGA (alpha-N-acetylgalactosaminidase) deficiency type 1
+BMGC_DS10202,BMG_DS038103,,"GRISCELLI SYNDROME, TYPE 3",,,,,DOID:0060834,Griscelli syndrome type 3,C1836573,,606526;609227,MONDO:0012220,Griscelli syndrome type 3,
+BMGC_DS10203,BMG_DS038104,,"Spondyloepiphyseal Dysplasia Tarda, Autosomal Recessive, Leroy-Spranger Type",,,,,,,C1836584,C563772,609223,MONDO:0012219,"spondyloepiphyseal dysplasia tarda, autosomal recessive, Leroy-Spranger type",
+BMGC_DS10204,BMG_DS038105,,Bruck syndrome 2,,,,,,,C1836602,C537407,609220,MONDO:0012217,Bruck syndrome 2,
+BMGC_DS10205,BMG_DS038106,,Foveal Hypoplasia and Anterior Segment Dysgenesis,,,,,,,C1836603,C563774,,,,
+BMGC_DS10206,BMG_DS038107,,Glucocorticoid Deficiency 3,,,,,,,C1836621,C563776,609197,MONDO:0012214,glucocorticoid deficiency 3,
+BMGC_DS10207,BMG_DS038108,,"Spastic paraplegia 26, autosomal recessive",,,,,,,C1836632,C536862,609195,MONDO:0012213,hereditary spastic paraplegia 26,
+BMGC_DS10208,BMG_DS038109,,Loeys-Dietz Aortic Aneurysm Syndrome,Loeys-Dietz Syndrome,,,,DOID:0050466,Loeys-Dietz syndrome,C1836635,D055947,,,,
+BMGC_DS10209,BMG_DS038110,,"Dissection, Ascending Aorta","Dissection, Ascending Aorta",,,,,,C1836653,D000094630,,,,
+BMGC_DS10210,BMG_DS038111,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If",,,,,DOID:0080558,congenital disorder of glycosylation If,C1836669,,604041;609180,MONDO:0012211,MPDU1-congenital disorder of glycosylation,
+BMGC_DS10211,BMG_DS038113,,"Total Hypotrichosis, Mari type",,,,,,,C1836672,C536973,604379,MONDO:0011452,hypotrichosis 7,
+BMGC_DS10212,BMG_DS038114,,Branchiogenic-Deafness Syndrome,,,,,,,C1836673,C563780,609166,MONDO:0012209,branchiogenic deafness syndrome,
+BMGC_DS10213,BMG_DS038117,,,,,,,,,C1836683,,609162,MONDO:0012206,spondyloepiphyseal dysplasia with metatarsal shortening,
+BMGC_DS10214,BMG_DS038118,,"Striatal Degeneration, Autosomal Dominant",,,,,,,C1836694,C563783,,MONDO:0000211,"striatal degeneration, autosomal dominant",
+BMGC_DS10215,BMG_DS038120,,"Pseudohyperkalemia, Familial, 2, due to Red Cell Leak",,,,,,,C1836705,C563785,609153,MONDO:0012204,familial pseudohyperkalemia,
+BMGC_DS10216,BMG_DS038121,,"Hyperthyroidism, Nonautoimmune",,,,,,,C1836706,C563786,609152,MONDO:0012203,familial hyperthyroidism due to mutations in TSH receptor,
+BMGC_DS10217,BMG_DS038122,,,,,,,,,C1836721,,609148,MONDO:0012202,"malaria, mild, susceptibility to",
+BMGC_DS10218,BMG_DS038124,,"Corneal Dystrophy, Posterior Polymorphous, 3",,,,,,,C1836724,C563788,609141,MONDO:0012200,posterior polymorphous corneal dystrophy 3,
+BMGC_DS10219,BMG_DS038125,,"Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease",,,,,,,C1836727,C563789,609136,MONDO:0012198,PCWH syndrome,
+BMGC_DS10220,BMG_DS038126,,,,,,,,,C1836743,,609129,MONDO:0012196,autosomal dominant auditory neuropathy 1,
+BMGC_DS10221,BMG_DS038127,,"Arthrogryposis, Distal, Type 4",,,,,DOID:0111610,distal arthrogryposis type 4,C1836756,C563791,609128,MONDO:0012195,arthrogryposis-severe scoliosis syndrome,
+BMGC_DS10222,BMG_DS038128,,"ANEURYSM, INTRACRANIAL BERRY, 3",,,,,DOID:0080966,intracranial berry aneurysm 3,C1836757,,609122,MONDO:0012194,"aneurysm, intracranial berry, 3",
+BMGC_DS10223,BMG_DS038130,,"Limb-Girdle Muscular Dystrophy, Type 1G",,,,,,,C1836765,C563794,609115,MONDO:0012193,autosomal dominant limb-girdle muscular dystrophy type 1G,
+BMGC_DS10224,BMG_DS038131,,"TELOMERE LENGTH, MEAN LEUKOCYTE",,,,,,,C1836777,,609113,,,
+BMGC_DS10225,BMG_DS038132,,PANCREATIC AND CEREBELLAR AGENESIS,,,,,,,C1836780,,609069;607194,MONDO:0012192,permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome,
+BMGC_DS10226,BMG_DS038133,,Combined Oxidative Phosphorylation Deficiency 1,,,,,DOID:0111474,combined oxidative phosphorylation deficiency 1,C1836797,C563797,609060,MONDO:0012191,hepatoencephalopathy due to combined oxidative phosphorylation defect type 1,
+BMGC_DS10227,BMG_DS038134,,Nephropathy with Pretibial Epidermolysis Bullosa and Deafness,,,,,,,C1836823,C563798,609057,MONDO:0012190,"epidermolysis bullosa simplex 7, with nephropathy and deafness",
+BMGC_DS10228,BMG_DS038135,,Amish Infantile Epilepsy Syndrome,,,,,,,C1836824,C563799,609056,MONDO:0018274,GM3 synthase deficiency,
+BMGC_DS10229,BMG_DS038136,609225004,Developmental regression,,,,,,,C1836830,,MTHU001319,,,Developmental regression | Developmental regression (disorder)
+BMGC_DS10230,BMG_DS038137,,"Ceroid lipofuscinosis, neuronal 9",,,,,,,C1836841,C537953,609055,MONDO:0012188,neuronal ceroid lipofuscinosis 9,
+BMGC_DS10231,BMG_DS038138,,"FANCONI ANEMIA, COMPLEMENTATION GROUP J",,,,,DOID:0111097,Fanconi anemia complementation group J,C1836860,,605882;609054,MONDO:0012187,Fanconi anemia complementation group J,
+BMGC_DS10232,BMG_DS038139,,"FANCONI ANEMIA, COMPLEMENTATION GROUP I",,,,,DOID:0111091,Fanconi anemia complementation group I,C1836861,,609053;611360,MONDO:0012186,Fanconi anemia complementation group I,
+BMGC_DS10233,BMG_DS038140,,"Spondylometaphyseal Dysplasia, Type A4",,,,,DOID:0112301,spondylometaphyseal dysplasia type A4,C1836862,C563803,609052,MONDO:0012185,"spondylometaphyseal dysplasia, A4 type",
+BMGC_DS10234,BMG_DS038141,723449004,Pierson syndrome,,,,,DOID:0060852,Pierson syndrome,C1836876,C537185,609049,MONDO:0012184,Pierson syndrome,Pierson syndrome (disorder) | Pierson syndrome | Microcoria and congenital nephrosis syndrome
+BMGC_DS10235,BMG_DS038142,,,,,,,,,C1836892,,609048,MONDO:0012183,"melanoma, cutaneous malignant, susceptibility to, 3",
+BMGC_DS10236,BMG_DS038144,,"Spastic Paraplegia 27, Autosomal Recessive",,,,,,,C1836899,C563807,609041,MONDO:0012181,hereditary spastic paraplegia 27,
+BMGC_DS10237,BMG_DS038145,,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 9",,,,,,,C1836906,C563808,609040,MONDO:0012180,arrhythmogenic right ventricular dysplasia 9,
+BMGC_DS10238,BMG_DS038146,,NARCOLEPSY 3,,,,,,,C1836907,,609039,MONDO:0012179,narcolepsy 3,
+BMGC_DS10239,BMG_DS038147,,"Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature",,,,,,,C1836915,C563810,609037,MONDO:0012178,"intellectual disability with optic atrophy, facial dysmorphism, microcephaly, and short stature",
+BMGC_DS10240,BMG_DS038148,,POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA,,,,,,,C1836916,,609033;609144,MONDO:0012177,posterior column ataxia-retinitis pigmentosa syndrome,
+BMGC_DS10241,BMG_DS038149,702417004,Emanuel syndrome,,,,,,,C1836929,C535733,609029,MONDO:0012176,Emanuel syndrome,Der(22) syndrome due to 3:1 meiotic disjunction events | Supernumerary der(22)t(11;22) syndrome | Supernumerary derivative 22 chromosome syndrome | Emanuel syndrome | Supernumerary der(22)t(11;22) syndrome (disorder) | Supernumerary der(22) syndrome
+BMGC_DS10242,BMG_DS038151,,Peripheral Cone Dystrophy,,,,,,,C1836946,C563813,609021,MONDO:0012174,peripheral cone dystrophy,
+BMGC_DS10243,BMG_DS038152,,Marfanoid Habitus with Situs Inversus,,,,,,,C1836994,C563814,609008,MONDO:0012171,marfanoid habitus with situs inversus,
+BMGC_DS10244,BMG_DS038153,,"DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT",,,,,,,C1837007,,609006,MONDO:0012170,autosomal recessive nonsyndromic hearing loss 36,
+BMGC_DS10245,BMG_DS038154,,Premature Ovarian Failure 3,,,,,,,C1837008,C563816,608996,MONDO:0012169,premature ovarian failure 3,
+BMGC_DS10246,BMG_DS038155,,,,,,,,,C1837009,,608995,MONDO:0012168,"dyslexia, susceptibility to, 8",
+BMGC_DS10247,BMG_DS038156,,"Atrial Fibrillation, Familial, 3",,,,,,,C1837014,C563817,607554,MONDO:0011857,"atrial fibrillation, familial, 3",
+BMGC_DS10248,BMG_DS038157,,,,,,,,,C1837015,,608984,MONDO:0012166,autosomal dominant sensory ataxia 1,
+BMGC_DS10249,BMG_DS038158,,"CATARACT, CONGENITAL, CERULEAN TYPE, 3",,,,,,,C1837023,,115700,,,
+BMGC_DS10250,BMG_DS038159,,,,,,,,,C1837026,,608978,MONDO:0012164,Meacham syndrome,
+BMGC_DS10251,BMG_DS038160,,"Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive",,,,,DOID:0090014,"severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive",C1837028,C563822,,,,
+BMGC_DS10252,BMG_DS038161,,"Macular Dystrophy, Butterfly-Shaped Pigmentary, 2",,,,,,,C1837029,C536309,608970,MONDO:0012162,patterned macular dystrophy 2,
+BMGC_DS10253,BMG_DS038162,,"CD8 Deficiency, Familial",,,,,,,C1837065,C563824,608957,MONDO:0012161,susceptibility to respiratory infections associated with CD8alpha chain mutation,
+BMGC_DS10254,BMG_DS038163,,Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy,,,,,DOID:0112300,spondylometaphyseal dysplasia with cone-rod dystrophy,C1837073,C563825,608940,MONDO:0012160,spondylometaphyseal dysplasia-cone-rod dystrophy syndrome,
+BMGC_DS10255,BMG_DS038166,,,,,,,,,C1837091,,608931,MONDO:0012157,congenital myasthenic syndrome 4C,
+BMGC_DS10256,BMG_DS038167,,"Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency",,,,,,,C1837092,C563829,,,,
+BMGC_DS10257,BMG_DS038168,,"Myasthenic Syndrome, Congenital, Fast-Channel",,,,,,,C1837122,C563832,,,,
+BMGC_DS10258,BMG_DS038169,,Myopia 6,,,,,,,C1837148,C536105,608908,MONDO:0012154,myopia 6,
+BMGC_DS10259,BMG_DS038170,,Alzheimer Disease 9,,,,,,,C1837149,C563834,,,,
+BMGC_DS10260,BMG_DS038175,,"Drug Metabolism, Poor, CYP2D6-Related",,,,,,,C1837154,C563835,608902,MONDO:0012148,"obsolete drug metabolism, poor, CYP2D6-related",
+BMGC_DS10261,BMG_DS038176,,,,,,,,,C1837173,,608901,MONDO:0012147,"coronary heart disease, susceptibility to, 5",
+BMGC_DS10262,BMG_DS038177,,"HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3",,,,,DOID:0110923,familial hemophagocytic lymphohistiocytosis 3,C1837174,,608897;608898,MONDO:0012146,familial hemophagocytic lymphohistiocytosis 3,
+BMGC_DS10263,BMG_DS038178,,"MACULAR DEGENERATION, AGE-RELATED, 3",,,,,,,C1837187,,604580;608895,MONDO:0012145,"macular degeneration, age-related, 3",
+BMGC_DS10264,BMG_DS038179,,,,,,,,,C1837203,,608890,MONDO:0012144,Waardenburg syndrome type 2D,
+BMGC_DS10265,BMG_DS038180,,"Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly",,,,,,,C1837206,C563840,608885,MONDO:0012143,hereditary cryohydrocytosis with reduced stomatin,
+BMGC_DS10266,BMG_DS038181,,OROFACIAL CLEFT 5,,,,,,,C1837210,,608874;142983,MONDO:0012142,orofacial cleft 5,
+BMGC_DS10267,BMG_DS038182,,,,,,,,,C1837213,,608864,MONDO:0012141,"orofacial cleft 6, susceptibility to",
+BMGC_DS10268,BMG_DS038183,,,,,,,,,C1837218,,119540,MONDO:0007336,isolated cleft palate,
+BMGC_DS10269,BMG_DS038184,,"Muscular Dystrophy, Congenital, Type 1D",,,,,,,C1837229,C563844,608840,MONDO:0012138,muscular dystrophy-dystroglycanopathy type B6,
+BMGC_DS10270,BMG_DS038185,,Carney Complex Variant,,,,,,,C1837245,C563845,608837,MONDO:0012137,Carney complex - trismus - pseudocamptodactyly syndrome,
+BMGC_DS10271,BMG_DS038189,,"MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 3",,,,,DOID:0111326,juvenile myoclonic epilepsy 3,C1837308,,608816,MONDO:0012134,"myoclonic epilepsy, juvenile, susceptibility to, 3",
+BMGC_DS10272,BMG_DS038191,,,,,,,,,C1837315,,608812,MONDO:0012132,"colorectal cancer, susceptibility to, 1",
+BMGC_DS10273,BMG_DS038193,,Alpha-B Crystallinopathy,,,,,,,C1837317,C563848,608810,MONDO:0012130,myofibrillar myopathy 2,
+BMGC_DS10274,BMG_DS038196,,,,,,,,,C1837341,,608808,MONDO:0012128,"transposition of the great arteries, dextro-looped",
+BMGC_DS10275,BMG_DS038197,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J",,,,,,,C1837342,,608807,MONDO:0012127,autosomal recessive limb-girdle muscular dystrophy type 2J,
+BMGC_DS10276,BMG_DS038198,,"Leukodystrophy, Hypomyelinating, 2",,,,,,,C1837355,C563855,608804,MONDO:0012125,hypomyelinating leukodystrophy 2,
+BMGC_DS10277,BMG_DS038199,,Sudden Infant Death with Dysgenesis of the Testes Syndrome,,,,,,,C1837371,C563856,608800,MONDO:0012124,sudden infant death-dysgenesis of the testes syndrome,
+BMGC_DS10278,BMG_DS038200,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie",,,,,DOID:0080557,congenital disorder of glycosylation Ie,C1837396,,603503;608799,MONDO:0012123,congenital disorder of glycosylation type 1E,
+BMGC_DS10279,BMG_DS038202,,OTOSCLEROSIS 5,,,,,DOID:0060924,otosclerosis 5,C1837422,,608787,MONDO:0012121,otosclerosis 5,
+BMGC_DS10280,BMG_DS038203,1003847003,Pyruvate dehydrogenase phosphatase deficiency,,,,,,,C1837429,C536258,608782,MONDO:0012120,pyruvate dehydrogenase phosphatase deficiency,Pyruvate dehydrogenase phosphatase deficiency (disorder) | Pyruvate dehydrogenase phosphatase deficiency
+BMGC_DS10281,BMG_DS038205,,SPINOCEREBELLAR ATAXIA 8,,,,,DOID:0050959,spinocerebellar ataxia type 8,C1837454,,603680;608768;613289,MONDO:0012116,spinocerebellar ataxia type 8,
+BMGC_DS10282,BMG_DS038206,,,,,,,,,C1837461,,608765,MONDO:0012115,"scoliosis, isolated, susceptibility to, 3",
+BMGC_DS10283,BMG_DS038208,,,,,,,,,C1837468,,608762,MONDO:0012113,"epilepsy, idiopathic generalized, susceptibility to, 3",
+BMGC_DS10284,BMG_DS038209,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8",,,,,DOID:0110314,hypertrophic cardiomyopathy 8,C1837471,,160790;608751,MONDO:0012111,hypertrophic cardiomyopathy 8,
+BMGC_DS10285,BMG_DS038210,,Insulin-Like Growth Factor I Deficiency,,,,,,,C1837475,C563867,608747,MONDO:0012110,growth delay due to insulin-like growth factor type 1 deficiency,
+BMGC_DS10286,BMG_DS038212,,"Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related",,,,,,,C1837481,C563869,608728,MONDO:0012108,"spondyloepimetaphyseal dysplasia, matrilin-3 type",
+BMGC_DS10287,BMG_DS038214,,"Microcephaly, Primary Autosomal Recessive, 5",,,,,,,C1837501,C563871,608716,MONDO:0012106,"microcephaly 5, primary, autosomal recessive",
+BMGC_DS10288,BMG_DS038215,,Spinocerebellar ataxia 25,,,,,DOID:0050974,spinocerebellar ataxia type 25,C1837518,C537202,608703,MONDO:0012103,spinocerebellar ataxia type 25,
+BMGC_DS10289,BMG_DS038219,,AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency,,,,,,,C1837530,C563876,608688,MONDO:0012099,AICA-ribosiduria,
+BMGC_DS10290,BMG_DS038220,,SPINOCEREBELLAR ATAXIA 20,,,,,DOID:0050971,spinocerebellar ataxia type 20,C1837541,,608687,MONDO:0012098,spinocerebellar ataxia type 20,
+BMGC_DS10291,BMG_DS038221,,"Spondylocostal Dysostosis 2, Autosomal Recessive",,,,,,,C1837549,C535781,608681,MONDO:0012097;MONDO:0010180,"spondylocostal dysostosis 2, autosomal recessive | autosomal recessive spondylocostal dysostosis",
+BMGC_DS10292,BMG_DS038222,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L",,,,,,,C1837552,,608014;608673,MONDO:0012096,Charcot-Marie-Tooth disease axonal type 2L,
+BMGC_DS10293,BMG_DS038223,,Robin Sequence with Distinctive Facial Appearance and Brachydactyly,,,,,,,C1837564,C563880,608670,MONDO:0012095,intellectual disability-brachydactyly-Pierre Robin syndrome,
+BMGC_DS10294,BMG_DS038226,,"DEAFNESS, AUTOSOMAL RECESSIVE 32",,,,,,,C1837608,,603504;608653,MONDO:0012091,autosomal recessive nonsyndromic hearing loss 32,
+BMGC_DS10295,BMG_DS038227,,"Deafness, Autosomal Dominant 47",,,,,,,C1837609,C563885,608652,MONDO:0012090,autosomal dominant nonsyndromic hearing loss 47,
+BMGC_DS10296,BMG_DS038228,,ICHTHYOSIS PREMATURITY SYNDROME,,,,,,,C1837610,,604194;608649,MONDO:0012089,ichthyosis prematurity syndrome,
+BMGC_DS10297,BMG_DS038229,,"Ciliary Dyskinesia, Primary, 5",,,,,,,C1837615,C563886,608647,MONDO:0012088,primary ciliary dyskinesia 5,
+BMGC_DS10298,BMG_DS038231,,"Deafness, Autosomal Dominant 31",,,,,,,C1837617,C563888,608645,MONDO:0012086,autosomal dominant nonsyndromic hearing loss 31,
+BMGC_DS10299,BMG_DS038232,,"CILIARY DYSKINESIA, PRIMARY, 3",,,,,,,C1837618,,608644;603335,MONDO:0012085,primary ciliary dyskinesia 3,
+BMGC_DS10300,BMG_DS038233,,"Deafness, Autosomal Dominant 28",,,,,,,C1837640,C563890,608641,MONDO:0012083,autosomal dominant nonsyndromic hearing loss 28,
+BMGC_DS10301,BMG_DS038234,,"ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1",,,,,,,C1837646,,608638,MONDO:0012082,"asperger syndrome, susceptibility to, 1",
+BMGC_DS10302,BMG_DS038235,702400006,"Spondyloepiphyseal dysplasia, Omani type",,,,,,,C1837657,C535789,143095,MONDO:0007738,spondyloepiphyseal dysplasia with congenital joint dislocations,"Spondyloepiphyseal dysplasia, Omani type | Humero-spinal dysostosis | Spondyloepiphyseal dysplasia with congenital joint dislocations (disorder) | Autosomal recessive Larsen syndrome | Spondyloepiphyseal dysplasia with congenital joint dislocations"
+BMGC_DS10303,BMG_DS038236,430099007,Gross motor development delay,,,,,,,C1837658,,MTHU074460,,,Gross motor development delay (disorder) | Gross motor development delay
+BMGC_DS10304,BMG_DS038237,,"ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2",,,,,,,C1837697,,608631,MONDO:0012079,"asperger syndrome, susceptibility to, 2",
+BMGC_DS10305,BMG_DS038238,,JOUBERT SYNDROME 3,,,,,,,C1837713,,608629;608894,MONDO:0012078,Joubert syndrome 3,
+BMGC_DS10306,BMG_DS038239,,Amyotrophic Lateral Sclerosis 8,,,,,,,C1837728,C563895,608627,MONDO:0012077,amyotrophic lateral sclerosis type 8,
+BMGC_DS10307,BMG_DS038240,,"Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia",,,,,,,C1837730,C563896,608624,MONDO:0012076,"midface hypoplasia, obesity, developmental delay, and neonatal hypotonia",
+BMGC_DS10308,BMG_DS038241,,"Hypertension, Diastolic, Resistance to",,,,,,,C1837739,C563897,,,,
+BMGC_DS10309,BMG_DS038242,,,,,,,,,C1837750,,608615,MONDO:0012075,oligodontia-cancer predisposition syndrome,
+BMGC_DS10310,BMG_DS038243,,MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY,,,,,DOID:0081129,mandibuloacral dysplasia type B lipodystrophy,C1837756,,608612;606480,MONDO:0012074,mandibuloacral dysplasia with type B lipodystrophy,
+BMGC_DS10311,BMG_DS038245,,"Charcot-Marie-Tooth disease, axonal, Type 2G",,,,,,,C1837805,C539595,,,,
+BMGC_DS10312,BMG_DS038248,,,,,,,,,C1837811,,608584,MONDO:0012067,"asthma-related traits, susceptibility to, 2",
+BMGC_DS10313,BMG_DS038249,,"Atrial Fibrillation, Familial, 2",,,,,,,C1837812,C563903,608988,MONDO:0012167,"atrial fibrillation, familial, 2",
+BMGC_DS10314,BMG_DS038251,,Burn-Mckeown syndrome,,,,,DOID:0080695,Burn-McKeown syndrome,C1837822,C537411,608572,MONDO:0012064,choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome,
+BMGC_DS10315,BMG_DS038253,,Ulnar-Fibular Ray Defect and Brachydactyly,,,,,,,C1837830,C563905,608571,MONDO:0012063,ulnar/fibula ray defect-brachydactyly syndrome,
+BMGC_DS10316,BMG_DS038254,,"CARDIOMYOPATHY, DILATED, 1O",,,,,,,C1837839,,601439;608569,MONDO:0012062,dilated cardiomyopathy 1O,
+BMGC_DS10317,BMG_DS038255,,,,,,,,,C1837845,,608567,MONDO:0024562,sick sinus syndrome 1,
+BMGC_DS10318,BMG_DS038256,,"DEAFNESS, AUTOSOMAL RECESSIVE 35",,,,,,,C1837857,,608565;602167,MONDO:0012060,autosomal recessive nonsyndromic hearing loss 35,
+BMGC_DS10319,BMG_DS038259,,,,,,,,,C1837872,,608556,MONDO:0012057,"legionnaire disease, susceptibility to",
+BMGC_DS10320,BMG_DS038260,,Leber Congenital Amaurosis 9,,,,,,,C1837873,C536603,608553,MONDO:0012056,Leber congenital amaurosis 9,
+BMGC_DS10321,BMG_DS038261,,Larsen-Like Syndrome,,,,,,,C1837884,C563914,608545,MONDO:0012055,Larsen-like osseous dysplasia-short stature syndrome,
+BMGC_DS10322,BMG_DS038262,,SCHIZOPHRENIA 12,,,,,DOID:0070088,schizophrenia 12,C1837893,,608543,MONDO:0012054,schizophrenia 12,
+BMGC_DS10323,BMG_DS038263,,"Aneurysm, intracranial berry, 2",,,,,,,C1837894,C536360,608542,MONDO:0012053,"aneurysm, intracranial berry, 2",
+BMGC_DS10324,BMG_DS038264,,"ERYTHROCYTOSIS, FAMILIAL, 2",,,,,,,C1837915,,608537;263400,MONDO:0009892,Chuvash polycythemia,
+BMGC_DS10325,BMG_DS038268,,Myopia 5,,,,,,,C1837972,C563922,608474,MONDO:0012045,"myopia 5, autosomal dominant",
+BMGC_DS10326,BMG_DS038269,,"Corneal Dystrophy, Lattice Type IIIA",,,,,,,C1837974,C563923,608471,MONDO:0012044,"corneal dystrophy, lattice type 3A",
+BMGC_DS10327,BMG_DS038270,,Knobloch Syndrome Type II,,,,,,,C1838009,C548030,,,,
+BMGC_DS10328,BMG_DS038273,,,,,,,,,C1838023,,608443,MONDO:0012037,"intellectual disability, autosomal recessive 3",
+BMGC_DS10329,BMG_DS038274,,"Epilepsy, Nocturnal Frontal Lobe, Type 1",,,,,,,C1838049,C563930,600513,MONDO:0010899,autosomal dominant nocturnal frontal lobe epilepsy 1,
+BMGC_DS10330,BMG_DS038275,,Autosomal Dominant Lateral Temporal Lobe Epilepsy,,,,,,,C1838062,C537297,,MONDO:0010898,autosomal dominant epilepsy with auditory features,
+BMGC_DS10331,BMG_DS038276,,,,,,,,,C1838069,,600511,MONDO:0010897,schizophrenia 3,
+BMGC_DS10332,BMG_DS038277,,ABCD syndrome,,,,,DOID:0050600,ABCD syndrome,C1838099,C535334,600501,MONDO:0010895,ABCD syndrome,
+BMGC_DS10333,BMG_DS038278,,,,,,,,,C1838100,,600496,MONDO:0010894,maturity-onset diabetes of the young type 3,
+BMGC_DS10334,BMG_DS038279,,,,,,,,,C1838102,,600467,MONDO:0010893,"malignant hyperthermia, susceptibility to, 4",
+BMGC_DS10335,BMG_DS038280,,MITOCHONDRIAL MYOPATHY AND SIDEROBLASTIC ANEMIA,,,,,DOID:0111185,"myopathy, lactic acidosis, and sideroblastic anemia 1",C1838103,,600462,MONDO:0000863,"myopathy, lactic acidosis, and sideroblastic anemia",
+BMGC_DS10336,BMG_DS038283,,"Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly",,,,,DOID:0070419,acrocardiofacial syndrome,C1838121,C563936,600460,MONDO:0010890,acrocardiofacial syndrome,
+BMGC_DS10337,BMG_DS038284,,Arterial Dissection with Lentiginosis,,,,,,,C1838122,C563937,600459,MONDO:0010889,arterial dissection-lentiginosis syndrome,
+BMGC_DS10338,BMG_DS038285,,"Hypertrichosis, anterior cervical",,,,,,,C1838123,C538390,600457,MONDO:0010887,isolated anterior cervical hypertrichosis,
+BMGC_DS10339,BMG_DS038286,,Angiokeratoma Corporis Diffusum with Arteriovenous Fistulas,,,,,,,C1838141,C563940,600419,MONDO:0010885,angiokeratoma corporis diffusum with arteriovenous fistulas,
+BMGC_DS10340,BMG_DS038288,,"Aphalangia, Partial, with Syndactyly and Duplication of Metatarsal IV",,,,,,,C1838161,C563942,600384,MONDO:0010882,aphalangy-syndactyly-microcephaly syndrome,
+BMGC_DS10341,BMG_DS038289,,Mesomelia-synostoses syndrome,,,,,,,C1838162,C537348,600383,MONDO:0010881,mesomelia-synostoses syndrome,
+BMGC_DS10342,BMG_DS038290,,,,,,,,,C1838163,,600376,MONDO:0010880,"telangiectasia, hereditary hemorrhagic, type 2",
+BMGC_DS10343,BMG_DS038291,717772000,CODAS syndrome,,,,,DOID:0111274,CODAS syndrome,C1838180,C536434,600373,MONDO:0010879,CODAS syndrome,Cerebro-oculo-dento-auriculo-skeletal syndrome (disorder) | Cerebro-oculo-dento-auriculo-skeletal syndrome | CODAS syndrome | CODAS (cerebro-oculo-dento-auriculo-skeletal) syndrome
+BMGC_DS10344,BMG_DS038292,,,,,,,DOID:0080314,cone-rod dystrophy 14,C1838190,,,,,
+BMGC_DS10345,BMG_DS038293,,"Spastic paraplegia 6, autosomal dominant",,,,,,,C1838192,C536866,600363,MONDO:0010878,hereditary spastic paraplegia 6,
+BMGC_DS10346,BMG_DS038294,,Aplasia cutis congenita of limbs recessive,,,,,,,C1838206,C536840,600360,MONDO:0010876,recessive aplasia cutis congenita of limbs,
+BMGC_DS10347,BMG_DS038295,,"Pachydermodactyly, Familial",,,,,,,C1838218,C563947,600356,MONDO:0010875,"pachydermodactyly, familial",
+BMGC_DS10348,BMG_DS038296,,"SPINAL MUSCULAR ATROPHY, TYPE IV",,,,,DOID:0050529,adult spinal muscular atrophy,C1838230,,271150;600354,MONDO:0010056,"spinal muscular atrophy, type IV",
+BMGC_DS10349,BMG_DS038298,,Band Heterotopia of Brain,,,,,,,C1838239,C563950,,,,
+BMGC_DS10350,BMG_DS038300,,Succinic Acidemia,,,,,,,C1838243,C563952,600335,MONDO:0010871,succinic acidemia,
+BMGC_DS10351,BMG_DS038301,,"TIBIAL MUSCULAR DYSTROPHY, TARDIVE",,,,,DOID:0111078,tibial muscular dystrophy,C1838244,,600334;188840,MONDO:0010870,tibial muscular dystrophy,
+BMGC_DS10352,BMG_DS038303,,RIPPLING MUSCLE DISEASE 1,,,,,,,C1838254,,600332,MONDO:0010868,rippling muscle disease 1,
+BMGC_DS10353,BMG_DS038304,771186004,PARC syndrome,,,,,,,C1838256,C537174,600331,MONDO:0010867,PARC syndrome,"PARC syndrome | Poikiloderma, alopecia, retrognathism, cleft palate syndrome (disorder) | Poikiloderma, alopecia, retrognathism, cleft palate syndrome | PARC (poikiloderma, alopecia, retrognathism, cleft palate) syndrome"
+BMGC_DS10354,BMG_DS038306,,Osteopetrosis and infantile neuroaxonal dystrophy,,,,,,,C1838258,C536055,600329,MONDO:0010866,infantile osteopetrosis with neuroaxonal dysplasia,
+BMGC_DS10355,BMG_DS038308,,"DIABETES MELLITUS, INSULIN-DEPENDENT, 5",,,,,,,C1838260,,600320,MONDO:0010863,type 1 diabetes mellitus 5,
+BMGC_DS10356,BMG_DS038311,,"Deafness, Autosomal Recessive 3",,,,,,,C1838263,C563961,600316,MONDO:0010860,autosomal recessive nonsyndromic hearing loss 3,
+BMGC_DS10357,BMG_DS038312,,"Epiphyseal dysplasia, multiple, 1",,,,,DOID:0070303,multiple epiphyseal dysplasia 1,C1838280,C535501,132400,MONDO:0007561,multiple epiphyseal dysplasia type 1,
+BMGC_DS10358,BMG_DS038317,,"Polycystic kidneys, severe infantile with tuberous sclerosis",,,,,,,C1838327,C536328,600273,MONDO:0010856,autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis,
+BMGC_DS10359,BMG_DS038318,721075001,Lopes Gorlin syndrome,,,,,,,C1838328,C537036,600269,MONDO:0010855,short tarsus-absence of lower eyelashes syndrome,Short tarsus with absence of lower eyelashes syndrome (disorder) | Short tarsus with absence of lower eyelashes syndrome | Lopes Gorlin syndrome
+BMGC_DS10360,BMG_DS038319,,APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS,,,,,DOID:0111705,oculoectodermal syndrome,C1838329,,600268,MONDO:0010854,Toriello-Lacassie-Droste syndrome,
+BMGC_DS10361,BMG_DS038320,,"HELICOBACTER PYLORI INFECTION, SUSCEPTIBILITY TO",,,,,,,C1838332,,107470;600263,MONDO:0010853,"Helicobacter pylori infection, susceptibility to",
+BMGC_DS10362,BMG_DS038321,,"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4",,,,,DOID:0070275,hereditary nonpolyposis colorectal cancer type 4,C1838333,,614337,MONDO:0013699,Lynch syndrome 4,
+BMGC_DS10363,BMG_DS038322,,Bor-Duane hydrocephalus contiguous gene syndrome,,,,,,,C1838346,C536574,600257,MONDO:0010852,chromosome 8Q12.1-q21.2 deletion syndrome,
+BMGC_DS10364,BMG_DS038323,,"Hydrocephalus, Autosomal Dominant",,,,,,,C1838347,C563973,123155,MONDO:0007401,craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome,
+BMGC_DS10365,BMG_DS038324,763830009,Oculomaxillofacial dysostosis,,,,,,,C1838348,C537736,,MONDO:0015824,oculomaxillofacial dysostosis,Oculomaxillofacial dysostosis (disorder) | Richieri Costa Gorlin syndrome | Oculomaxillofacial dysostosis
+BMGC_DS10366,BMG_DS038325,,"Diffuse palmoplantar keratoderma, Bothnian type",,,,,DOID:0111707,Bothnian type palmoplantar keratoderma,C1838359,C536173,600231,MONDO:0010849,"palmoplantar keratoderma, Bothnian type",
+BMGC_DS10367,BMG_DS038326,,"Exostoses, Multiple, Type III",,,,,,,C1838420,C563975,600209,MONDO:0010846,"exostoses, multiple, type III",
+BMGC_DS10368,BMG_DS038327,,"Epiphyseal dysplasia, multiple, 2",,,,,,,C1838429,C535502,600204,MONDO:0010844,"epiphyseal dysplasia, multiple, 2",
+BMGC_DS10369,BMG_DS038328,,,,,,,,,C1838436,,600202,MONDO:0010843,"dyslexia, susceptibility to, 2",
+BMGC_DS10370,BMG_DS038329,,,,,,,DOID:0050792,multiple cutaneous and mucosal venous malformations,C1838437,,600195,MONDO:0010842,multiple cutaneous and mucosal venous malformations,
+BMGC_DS10371,BMG_DS038330,,ICHTHYOSIS EXFOLIATIVA,,,,,,,C1838440,,146800;600194,MONDO:0017339,exfoliative ichthyosis,
+BMGC_DS10372,BMG_DS038331,,Waardenburg syndrome type 2B,,,,,DOID:0110947,Waardenburg syndrome type 2B,C1838447,C536465,600193,MONDO:0010841,Waardenburg syndrome type 2B,
+BMGC_DS10373,BMG_DS038332,,"FANCONI ANEMIA, COMPLEMENTATION GROUP D1",,,,,DOID:0111089,Fanconi anemia complementation group D1,C1838457,,600185;605724,MONDO:0011584,Fanconi anemia complementation group D1,
+BMGC_DS10374,BMG_DS038333,763861000,Kuzniecky syndrome,,,,,,,C1838491,C538091,600176,MONDO:0010840,pachygyria-intellectual disability-epilepsy syndrome,"Pachygyria, intellectual disability, epilepsy syndrome (disorder) | Pachygyria, intellectual disability, epilepsy syndrome | Kuzniecky syndrome"
+BMGC_DS10375,BMG_DS038334,,"Spinal Muscular Atrophy, Distal, Congenital Nonprogressive",,,,,,,C1838492,C563981,600175,MONDO:0010839,"neuronopathy, distal hereditary motor, autosomal dominant 8",
+BMGC_DS10376,BMG_DS038335,,"Hyperparathyroidism, Primary, Caused By Water Clear Cell Hyperplasia",,,,,,,C1838501,C563982,600166,MONDO:0044350,"hyperparathyroidism, primary, caused by water clear cell hyperplasia",
+BMGC_DS10377,BMG_DS038336,,NANOPHTHALMOS 1,,,,,,,C1838502,,600165,MONDO:0010836,nanophthalmos 1,
+BMGC_DS10378,BMG_DS038337,,"CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE",,,,,DOID:0080662,atrial standstill 1,C1838539,,108770,,,
+BMGC_DS10379,BMG_DS038338,,MELANOMA-PANCREATIC CANCER SYNDROME,,,,,,,C1838547,,606719;600160,MONDO:0011713,melanoma-pancreatic cancer syndrome,
+BMGC_DS10380,BMG_DS038340,,,,,,,,,C1838564,,600155,MONDO:0010833,"Hirschsprung disease, susceptibility to, 2",
+BMGC_DS10381,BMG_DS038341,,Sacral defect and anterior sacral meningocele,,,,,,,C1838568,C537221,,,,
+BMGC_DS10382,BMG_DS038342,,"CEROID LIPOFUSCINOSIS, NEURONAL, 8",,,,,,,C1838570,,600143;607837,MONDO:0010830,neuronal ceroid lipofuscinosis 8,
+BMGC_DS10383,BMG_DS038343,,"Ceroid Lipofuscinosis, Neuronal, 7",,,,,,,C1838571,C563989,610951,MONDO:0012588,neuronal ceroid lipofuscinosis 7,
+BMGC_DS10384,BMG_DS038344,,Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy,,,,,,,C1838577,C563990,600142,MONDO:0010829,CARASIL syndrome,
+BMGC_DS10385,BMG_DS038345,,Retinitis Pigmentosa 11,,,,,DOID:0110408,retinitis pigmentosa 11,C1838601,C563991,600138,MONDO:0010828,retinitis pigmentosa 11,
+BMGC_DS10386,BMG_DS038346,,Retinitis Pigmentosa 14,,,,,DOID:0110381,retinitis pigmentosa 14,C1838603,C563992,600132,MONDO:0010827,retinitis pigmentosa 14,
+BMGC_DS10387,BMG_DS038347,,,,,,,,,C1838604,,600131,MONDO:0020759,"epilepsy, childhood absence, susceptibility to, 1",
+BMGC_DS10388,BMG_DS038351,,"Rhizomelic chondrodysplasia punctata, type 3",,,,,DOID:0110853,rhizomelic chondrodysplasia punctata type 3,C1838612,C537608,600121,MONDO:0010823,rhizomelic chondrodysplasia punctata type 3,
+BMGC_DS10389,BMG_DS038352,,WARBURG MICRO SYNDROME 1,,,,,DOID:0060237,Warburg micro syndrome,C1838625,,602536;600118,MONDO:0010822,Warburg micro syndrome 1,
+BMGC_DS10390,BMG_DS038353,,"Dysphasia, Familial Developmental",,,,,,,C1838630,C563997,600117,MONDO:0010821,familial developmental dysphasia,
+BMGC_DS10391,BMG_DS038354,,Stargardt disease 3,,,,,,,C1838644,C535805,600110,MONDO:0010819,Stargardt disease 3,
+BMGC_DS10392,BMG_DS038355,,Retinitis Pigmentosa 12,,,,,DOID:0110358,retinitis pigmentosa 12,C1838647,C563999,600105,MONDO:0010818,retinitis pigmentosa 12,
+BMGC_DS10393,BMG_DS038356,,SPLIT-HAND/FOOT MALFORMATION 3,,,,,,,C1838652,,246560,MONDO:0009525,split hand-foot malformation 3,
+BMGC_DS10394,BMG_DS038357,,Spondyloepiphyseal Dysplasia Tarda with Characteristic Facies,,,,,DOID:0112289,spondyloepiphyseal dysplasia tarda with characteristic facies,C1838653,C564003,600093,MONDO:0010815,spondyloepiphyseal dysplasia tarda with characteristic facies,
+BMGC_DS10395,BMG_DS038358,720851007,Nivelon Nivelon Mabille syndrome,,,,,DOID:0060644,chondrodysplasia-pseudohermaphroditism syndrome,C1838654,C536123,600092,MONDO:0010814,chondrodysplasia-pseudohermaphroditism syndrome,Chondrodysplasia with disorder of sex development syndrome (disorder) | Chondrodysplasia with disorder of sex development syndrome | Chondrodysplasia pseudohermaphroditism syndrome | Nivelon Nivelon Mabille syndrome
+BMGC_DS10396,BMG_DS038359,,Pancreatic beta cell agenesis with neonatal diabetes mellitus,,,,,,,C1838655,C538111,600089,MONDO:0010813,pancreatic beta cell agenesis with neonatal diabetes mellitus,
+BMGC_DS10397,BMG_DS038360,,"Macrocytosis, Familial",,,,,,,C1838656,C564004,600084,MONDO:0010812,"macrocytosis, familial",
+BMGC_DS10398,BMG_DS038361,,"Vitamin D Hydroxylation-Deficient Rickets, Type 1B",,,,,,,C1838657,C564005,600081,MONDO:0010810,"vitamin D hydroxylation-deficient rickets, type 1B",
+BMGC_DS10399,BMG_DS038362,,,,,,,,,C1838670,,600080,MONDO:0010809,familial chronic myelocytic leukemia-like syndrome,
+BMGC_DS10400,BMG_DS038363,,"DEAFNESS, AUTOSOMAL RECESSIVE 2",,,,,,,C1838701,,276903;600060,MONDO:0010807,autosomal recessive nonsyndromic hearing loss 2,
+BMGC_DS10401,BMG_DS038364,,Retinitis Pigmentosa 13,,,,,DOID:0110403,retinitis pigmentosa 13,C1838702,C564008,600059,MONDO:0010806,retinitis pigmentosa 13,
+BMGC_DS10402,BMG_DS038365,,Bladder Exstrophy and Epispadias Complex,,,,,,,C1838703,C564009,600057,MONDO:0700039,bladder exstrophy-epispadias-cloacal extrophy complex,
+BMGC_DS10403,BMG_DS038366,,Eiken Skeletal Dysplasia,,,,,DOID:0111732,Eiken syndrome,C1838779,C564010,600002,MONDO:0010803,Eiken syndrome,
+BMGC_DS10404,BMG_DS038368,,"Wolfram Syndrome, Mitochondrial Form",,,,,DOID:0080583,"Wolfram syndrome, mitochondrial form",C1838782,C564012,598500,MONDO:0010800,"Wolfram syndrome, mitochondrial form",
+BMGC_DS10405,BMG_DS038369,,"DEAFNESS, AMINOGLYCOSIDE-INDUCED",,,,,DOID:0111734,aminoglycoside-induced deafness,C1838854,,516030;580000;561000;590080,MONDO:0010799,"deafness, aminoglycoside-induced",
+BMGC_DS10406,BMG_DS038370,,"Parkinson Disease, Mitochondrial",,,,,,,C1838867,C564015,556500,MONDO:0010796,"Parkinson disease, mitochondrial",
+BMGC_DS10407,BMG_DS038372,,"MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE",,,,,,,C1838876,,551000,MONDO:0010792,lethal infantile mitochondrial myopathy,
+BMGC_DS10408,BMG_DS038373,,,,,,,,,C1838877,,550500,MONDO:0010791,"myoglobinuria, recurrent",
+BMGC_DS10409,BMG_DS038376,,"ATAXIA AND POLYNEUROPATHY, ADULT-ONSET",,,,,DOID:0111750,adult-onset ataxia and polyneuropathy,C1838916,,500010;516060,MONDO:0010781,"ataxia and polyneuropathy, adult-onset",
+BMGC_DS10410,BMG_DS038377,,LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY,,,,,,,C1838951,,516005;516006;516001,,,
+BMGC_DS10411,BMG_DS038378,,MITOCHONDRIAL COMPLEX I DEFICIENCY,,,,,DOID:0060536;DOID:0060536;DOID:0112074,mitochondrial complex I deficiency | nuclear type mitochondrial complex I deficiency 1 | mitochondrial complex I deficiency,C1838979,,516003;516001;252010,MONDO:0100133,mitochondrial complex I deficiency,
+BMGC_DS10412,BMG_DS038379,,,,,,,,,C1838989,,515000,MONDO:0010784,chloramphenicol toxicity,
+BMGC_DS10413,BMG_DS038380,,,,,,,,,C1838990,,502500,MONDO:0100295,"Alzheimer disease, susceptibility to, mitochondrial",
+BMGC_DS10414,BMG_DS038384,,"Striatonigral Degeneration, Infantile, Mitochondrial",,,,,,,C1839022,C564025,500003,MONDO:0010774,"striatonigral degeneration, infantile, mitochondrial",
+BMGC_DS10415,BMG_DS038385,,Mitochondrial Myopathy with Diabetes,,,,,,,C1839028,C564026,500002,MONDO:0010773,mitochondrial myopathy with diabetes,
+BMGC_DS10416,BMG_DS038386,,LEBER OPTIC ATROPHY AND DYSTONIA,,,,,DOID:0111755,Leber hereditary optic neuropathy and dystonia,C1839040,,516000;500001;516002;516003;516006,MONDO:0010772,Leber optic atrophy and dystonia,
+BMGC_DS10417,BMG_DS038388,,"Hairy Ears, Y-Linked",,,,,,,C1839070,C564029,425500,MONDO:0010769,"hairy ears, Y-linked",
+BMGC_DS10418,BMG_DS038389,,"Spermatogenic Failure, Nonobstructive, Y-Linked",,,,,DOID:0070187,Y-linked spermatogenic failure 2,C1839071,C564030,415000,MONDO:0010767,"spermatogenic failure, Y-linked, 2",
+BMGC_DS10419,BMG_DS038394,,"Retinitis Pigmentosa, Y-Linked",,,,,,,C1839079,C564035,400004,MONDO:0010761,retinitis pigmentosa Y-linked,
+BMGC_DS10420,BMG_DS038396,,,,,,,,,C1839082,,300848,MONDO:0010450,"intellectual disability, X-linked 89",
+BMGC_DS10421,BMG_DS038399,,"Von Willebrand Disease, X-Linked Form",,,,,,,C1839113,C564041,314560,MONDO:0010756,"Von Willebrand disease, X-linked form",
+BMGC_DS10422,BMG_DS038400,,"Vesicoureteral Reflux, X-Linked",,,,,,,C1839114,C564042,314550,MONDO:0010755,"vesicoureteral reflux, X-linked",
+BMGC_DS10423,BMG_DS038401,,UNIQUE GREEN PHENOMENON,,,,,,,C1839116,,314380,MONDO:0010751,unique green phenomenon,
+BMGC_DS10424,BMG_DS038403,733066002,Say Meyer syndrome,,,,,,,C1839125,C536620,314320,MONDO:0010749,trigonocephaly-short stature-developmental delay syndrome,"Trigonocephaly, short stature, developmental delay syndrome (disorder) | Trigonocephaly, short stature, developmental delay syndrome | Say Meyer syndrome"
+BMGC_DS10425,BMG_DS038404,,Torticollis keloids cryptorchidism renal dysplasia,,,,,,,C1839129,C536970,314300,MONDO:0010748,torticollis-keloids-cryptorchidism-renal dysplasia syndrome,
+BMGC_DS10426,BMG_DS038405,,"Dystonia 3, Torsion, X-Linked",,,,,,,C1839130,C564048,314250,MONDO:0010747,X-linked dystonia-parkinsonism,
+BMGC_DS10427,BMG_DS038406,,Thyroxine-Binding Globulin Deficiency,,,,,,,C1839141,C564049,,,,
+BMGC_DS10428,BMG_DS038407,,"Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis",,,,,DOID:0111767,X-linked thrombocytopenia with beta-thalassemia,C1839161,C564050,314050,MONDO:0010745,beta-thalassemia-X-linked thrombocytopenia syndrome,
+BMGC_DS10429,BMG_DS038408,,Thrombocytopenia with Elevated Serum Iga and Renal Disease,,,,,,,C1839162,C564051,314000,MONDO:0010744,thrombocytopenia with elevated serum IgA and renal disease,
+BMGC_DS10430,BMG_DS038409,,Thrombocytopenia 1,,,,,,,C1839163,C564052,313900,MONDO:0010743,thrombocytopenia 1,
+BMGC_DS10431,BMG_DS038412,,"Taurodontism, microdontia, and dens invaginatus",,,,,,,C1839235,C536947,313490,MONDO:0010740,"taurodontism, microdontia, and dens invaginatus",
+BMGC_DS10432,BMG_DS038414,,SPLIT-HAND/FOOT MALFORMATION 2,,,,,,,C1839258,,313350,MONDO:0010736,split hand-foot malformation 2,
+BMGC_DS10433,BMG_DS038415,,"Bulbo-Spinal Atrophy, X-Linked","Bulbo-Spinal Atrophy, X-Linked",,,,DOID:0060161,Kennedy's disease,C1839259,D055534,313200,MONDO:0010735,Kennedy disease,
+BMGC_DS10434,BMG_DS038416,,,,,,,,,C1839262,,313000,MONDO:0010734,"spatial visualization, aptitude for",
+BMGC_DS10435,BMG_DS038417,,"Spastic paraplegia 2, X-linked",,,,,,,C1839264,C536857,312920,MONDO:0010733,hereditary spastic paraplegia 2,
+BMGC_DS10436,BMG_DS038419,,Schimke X-linked mental retardation syndrome,,,,,,,C1839320,C536630,312840,MONDO:0010729,"X-linked intellectual disability, Schimke type",
+BMGC_DS10437,BMG_DS038420,734173003,SCARF syndrome,,,,,,,C1839321,C536625,312830,MONDO:0010728,SCARF syndrome,"SCARF (skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality) syndrome | SCARF syndrome | Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome | Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome (disorder)"
+BMGC_DS10438,BMG_DS038422,,Retinitis Pigmentosa 6,,,,,DOID:0110413,retinitis pigmentosa 6,C1839368,C564065,312612,MONDO:0000910,retinitis pigmentosa 6,
+BMGC_DS10439,BMG_DS038423,,Radiation Sensitivity of Natural Killer Activity,,,,,,,C1839408,C564066,312210,MONDO:0010719,radiation sensitivity of natural killer activity,
+BMGC_DS10440,BMG_DS038424,,Radius absent anogenital anomalies,,,,,,,C1839410,C535281,312190,MONDO:0010718,absent radius-anogenital anomalies syndrome,
+BMGC_DS10441,BMG_DS038425,,Pyruvate Dehydrogenase E1 Alpha Deficiency,,,,,,,C1839413,C564071,312170,MONDO:0010717,pyruvate dehydrogenase E1-alpha deficiency,
+BMGC_DS10442,BMG_DS038426,,Chronic lactic acidosis,,,,E87.22,,,C1839437,,,,,
+BMGC_DS10443,BMG_DS038427,,"Multiple Pterygium Syndrome, X-Linked",,,,,,,C1839440,C564072,312150,MONDO:0010716,X-linked lethal multiple pterygium syndrome,
+BMGC_DS10444,BMG_DS038428,,"PROPERDIN DEFICIENCY, X-LINKED",,,,,DOID:0111768,X-linked properdin deficiency,C1839454,,312060,MONDO:0010713,"properdin deficiency, X-linked",
+BMGC_DS10445,BMG_DS038429,,"Properdin Deficiency, Type II",,,,,,,C1839455,C564075,,,,
+BMGC_DS10446,BMG_DS038430,,"Properdin Deficiency, Type III",,,,,,,C1839456,C564076,,,,
+BMGC_DS10447,BMG_DS038431,725911008,TARP syndrome,,,,,DOID:0111780,TARP syndrome,C1839463,C536942,311900,MONDO:0010711,TARP syndrome,"Pierre Robin sequence, congenital heart defect, talipes syndrome (disorder) | TARP syndrome | Pierre Robin sequence, congenital heart defect, talipes syndrome | Pierre Robin syndrome, congenital heart defect, talipes syndrome | TARP (talipes equinovarus, atrial septal defect, Robin sequence, persistence of left superior vena cava) syndrome"
+BMGC_DS10448,BMG_DS038434,,Jensen syndrome,,,,,,,C1839564,C537568,,MONDO:0000501,obsolete Jensen syndrome,
+BMGC_DS10449,BMG_DS038435,,Optic Atrophy Spastic Paraplegia Syndrome,,,,,,,C1839565,C564084,311100,MONDO:0010700,optic atrophy--spastic paraplegia syndrome,
+BMGC_DS10450,BMG_DS038436,,"CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5",,,,,,,C1839566,,311070;311850,MONDO:0010699,Charcot-Marie-Tooth disease X-linked recessive 5,
+BMGC_DS10451,BMG_DS038437,721200000,Early-onset X-linked optic atrophy,,,,,,,C1839576,,311050,MONDO:0010698,optic atrophy 2,Early-onset X-linked optic atrophy (disorder) | Early-onset X-linked optic atrophy | Non-Leber type optic atrophy with early-onset | Optic atrophy type 2
+BMGC_DS10452,BMG_DS038438,,"Ophthalmoplegia, External, and Myopia",,,,,,,C1839577,C564087,311000,MONDO:0010697,"ophthalmoplegia, external, and myopia",
+BMGC_DS10453,BMG_DS038440,,"Nystagmus, Myoclonic",,,,,,,C1839579,C564088,310800,MONDO:0010694,"nystagmus, myoclonic",
+BMGC_DS10454,BMG_DS038441,,"Nystagmus 1, congenital, X- linked",,,,,,,C1839580,C537853,310700,MONDO:0010693,"nystagmus 1, congenital, X-linked",
+BMGC_DS10455,BMG_DS038443,,"Neuropathy, Hereditary Sensory, X-Linked",,,,,,,C1839602,C564090,310470,MONDO:0010688,hereditary sensory neuropathy X-linked,
+BMGC_DS10456,BMG_DS038445,,"MYOPIA 1, X-LINKED",,,,,,,C1839612,,310460,MONDO:0010685,"myopia 1, X-linked",
+BMGC_DS10457,BMG_DS038446,719815005,X-linked myopathy with excessive autophagy,,,,,,,C1839615,,310440,MONDO:0010684,X-linked myopathy with excessive autophagy,X-linked myopathy with excessive autophagy (disorder) | X-linked myopathy with excessive autophagy | Vacuolar myopathy
+BMGC_DS10458,BMG_DS038447,,MYELOLYMPHATIC INSUFFICIENCY,,,,,,,C1839650,,310350,MONDO:0010681,myelolymphatic insufficiency,
+BMGC_DS10459,BMG_DS038450,,"Muscular Dystrophy, Hemizygous Lethal Type",,,,,,,C1839671,C564097,309950,MONDO:0010676,"muscular dystrophy, Hemizygous lethal type",
+BMGC_DS10460,BMG_DS038451,,"Modifier, X-Linked, for Neurofunctional Defects",,,,,,,C1839708,C564098,309840,MONDO:0010673,"modifier, X-linked, for Neurofunctional defects",
+BMGC_DS10461,BMG_DS038454,,METACARPAL 4-5 FUSION,,,,,DOID:0111813,syndactyly type 8,C1839728,,300827;309630,MONDO:0010669,syndactyly type 8,
+BMGC_DS10462,BMG_DS038455,722478008,Skeletal dysplasia with intellectual disability syndrome,,,,,,,C1839729,,309620,MONDO:0010668,skeletal dysplasia-intellectual disability syndrome,Skeletal dysplasia with intellectual disability syndrome (disorder) | Skeletal dysplasia with intellectual disability syndrome | Christian syndrome
+BMGC_DS10463,BMG_DS038456,,Prieto syndrome,,,,,,,C1839730,C535274,309610,MONDO:0010667,Prieto syndrome,
+BMGC_DS10464,BMG_DS038457,,,,,,,DOID:0060815,Wieacker-Wolff syndrome,C1839735,,,,,
+BMGC_DS10465,BMG_DS038458,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, WILSON-TURNER TYPE",,,,,DOID:0060814,Wilson-Turner syndrome,C1839736,,300964;309585,MONDO:0010665,Wilson-Turner syndrome,
+BMGC_DS10466,BMG_DS038459,,FRAGILE X TREMOR/ATAXIA SYNDROME,,,,,DOID:0050879,fragile X-associated tremor/ataxia syndrome,C1839780,,300623;309550,MONDO:0010382,fragile X-associated tremor/ataxia syndrome,
+BMGC_DS10467,BMG_DS038460,,,,,,,,,C1839792,,309545,MONDO:0010658,syndromic X-linked intellectual disability 12,
+BMGC_DS10468,BMG_DS038461,,Noncompaction cardiomyopathy,,,,,,,C1839832,,MTHU025300,,,
+BMGC_DS10469,BMG_DS038462,,,,,,,,,C1839839,,309200,MONDO:0010648,major affective disorder 2,
+BMGC_DS10470,BMG_DS038463,,"Male Pseudohermaphroditism due to Deficiency of Testicular 17,20-Desmolase",,,,,,,C1839840,C564109,614279,MONDO:0013664,"46,XY disorder of sex development due to testicular 17,20-desmolase deficiency",
+BMGC_DS10471,BMG_DS038464,,"SPERMATOGENIC FAILURE, X-LINKED, 2",,,,,DOID:0070185,X-linked spermatogenic failure 2,C1839841,,309120;300311,MONDO:0010647,"spermatogenic failure, X-linked, 2",
+BMGC_DS10472,BMG_DS038465,,"Macular Dystrophy, X-Linked",,,,,,,C1839842,C564110,309100,MONDO:0010646,"macular dystrophy, X-linked",
+BMGC_DS10473,BMG_DS038466,,Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis,,,,,,,C1839874,C545036,308990,MONDO:0010644,"proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis",
+BMGC_DS10474,BMG_DS038467,,,,,,,,,C1839883,,308950,MONDO:0010642,Lesch-Nyhan phenotype with normal HGPRT,
+BMGC_DS10475,BMG_DS038468,,"Leiomyomatosis, esophageal and vulval, with nephropathy",,,,,,,C1839884,C537113,308940,MONDO:0010641,X-linked diffuse leiomyomatosis-Alport syndrome,
+BMGC_DS10476,BMG_DS038470,,,,,,,,,C1839891,,308905,MONDO:0010640,"Leber optic atrophy, susceptibility to",
+BMGC_DS10477,BMG_DS038471,,"CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED",,,,,,,C1839909,,304100;308840,MONDO:0010569,X-linked complicated corpus callosum dysgenesis,
+BMGC_DS10478,BMG_DS038472,,Keratosis follicularis dwarfism cerebral atrophy,,,,,,,C1839910,C536158,308830,MONDO:0010638,keratosis follicularis-dwarfism-cerebral atrophy syndrome,
+BMGC_DS10479,BMG_DS038473,,Spastic paraplegia with Kallmann syndrome,,,,,,,C1839911,C536873,308750,MONDO:0010636,Kallmann syndrome with spastic paraplegia,
+BMGC_DS10480,BMG_DS038474,,"Jaundice, Familial Obstructive, of Infancy",,,,,,,C1839927,C564118,308600,MONDO:0010634,"jaundice, familial obstructive, of infancy",
+BMGC_DS10481,BMG_DS038475,,IRIS HYPOPLASIA WITH GLAUCOMA,,,,,DOID:0080608,anterior segment dysgenesis 3,C1839928,,308500;601631,MONDO:0010633,iris hypoplasia with glaucoma,
+BMGC_DS10482,BMG_DS038477,,,,,,,,,C1839965,,308280,MONDO:0010629,"impacted teeth, multiple",
+BMGC_DS10483,BMG_DS038479,,"Immunodeficiency, X-Linked, with Deficiency of 115,000 Dalton Surface Glycoprotein",,,,,,,C1839982,C564120,308220,MONDO:0010625,"immunodeficiency, X-linked, with deficiency of 115,000 Dalton surface glycoprotein",
+BMGC_DS10484,BMG_DS038480,,Ichthyosis follicularis atrichia photophobia syndrome,,,,,DOID:0111821,ichthyosis follicularis-alopecia-photophobia syndrome 1,C1839988,C536085,,MONDO:0100212,IFAP syndrome,
+BMGC_DS10485,BMG_DS038483,,SMALL PATELLA SYNDROME,,,,,DOID:0111382,ischiocoxopodopatellar syndrome,C1840061,,147891,MONDO:0007841,coxopodopatellar syndrome,
+BMGC_DS10486,BMG_DS038484,,"Internal Carotid Artery, Spontaneous Dissection of",,,,,,,C1840073,C564125,147820,MONDO:0007840,"internal carotid artery, spontaneous dissection of",
+BMGC_DS10487,BMG_DS038485,,,,,,,,,C1840140,,147610,MONDO:0007833,"iris pigment layer, cleavage of",
+BMGC_DS10488,BMG_DS038487,,,,,,,,,C1840171,,147540,MONDO:0007831,"insect Stings, hypersensitivity to",
+BMGC_DS10489,BMG_DS038490,,,,,,,,,C1840224,,147350,MONDO:0007825,"incisors, rotation of upper central",
+BMGC_DS10490,BMG_DS038492,,,,,,,,,C1840235,,147250,MONDO:0007819,solitary median maxillary central incisor syndrome,
+BMGC_DS10491,BMG_DS038494,,"IgE RESPONSIVENESS, ATOPIC",,,,,,,C1840253,,147050,MONDO:0007817,"IgE responsiveness, atopic",
+BMGC_DS10492,BMG_DS038495,,IMMUNE SUPPRESSION,,,,,,,C1840264,,146850,,,
+BMGC_DS10493,BMG_DS038497,,"Immune Deficiency, Familial Variable",,,,,,,C1840266,C564136,146830,MONDO:0007814,"immune deficiency, familial variable",
+BMGC_DS10494,BMG_DS038498,,ICHTHYOSIS--CHEEK--EYEBROW SYNDROME,,,,,,,C1840283,,146720,MONDO:0007811,ichthyosis-cheek-eyebrow syndrome,
+BMGC_DS10495,BMG_DS038499,,LEBER CONGENITAL AMAUROSIS 11,,,,,,,C1840284,,146690;613837,MONDO:0013454,Leber congenital amaurosis 11,
+BMGC_DS10496,BMG_DS038500,,"Ichthyosis hystrix, Curth Macklin type",,,,,,,C1840296,C536088,146590,MONDO:0007808,ichthyosis hystrix of Curth-Macklin,
+BMGC_DS10497,BMG_DS038502,,Hypotrichosis Simplex of Scalp,,,,,,,C1840299,C564143,146520,MONDO:0007805,hypotrichosis 2,
+BMGC_DS10498,BMG_DS038503,,HYPOPHOSPHATEMIC BONE DISEASE,,,,,,,C1840321,,146350,MONDO:0007799,hypophosphatemic bone disease,
+BMGC_DS10499,BMG_DS038504,708672004,Odontohypophosphatasia,,,,,,,C1840322,C564146,,MONDO:0016607,odontohypophosphatasia,Odontohypophosphatasia (disorder) | Odontohypophosphatasia
+BMGC_DS10500,BMG_DS038505,724282009,Barakat syndrome,,,,,DOID:0060878,hypoparathyroidism-deafness-renal disease syndrome,C1840333,C537907,146255,MONDO:0007797,hypoparathyroidism-deafness-renal disease syndrome,"Hypoparathyroidism, deafness, renal disease syndrome (disorder) | Hypoparathyroidism, deafness, renal disease syndrome | Barakat syndrome | HDR (hypoparathyroidism, sensorineural deafness, renal disease) syndrome | HDR syndrome"
+BMGC_DS10501,BMG_DS038507,,Hypomelia mullerian duct anomalies,,,,,,,C1840335,C537155,146160,MONDO:0007795,mullerian duct anomalies-limb anomalies syndrome,
+BMGC_DS10502,BMG_DS038508,,"Hypocalciuric hypercalcemia, familial, type 2",,,,,,,C1840347,C537146,145981,MONDO:0007792,familial hypocalciuric hypercalcemia 2,
+BMGC_DS10503,BMG_DS038510,,Hypertrophia Musculorum Vera,,,,,,,C1840361,C564152,145800,MONDO:0007789,hypertrophia musculorum vera,
+BMGC_DS10504,BMG_DS038511,,Ambras syndrome,,,,,DOID:0111060,Ambras type hypertrichosis universalis congenita,C1840362,C536605,145701,MONDO:0007787,Ambras type hypertrichosis universalis congenita,
+BMGC_DS10505,BMG_DS038512,,"THYROID HORMONE RESISTANCE, SELECTIVE PITUITARY",,,,,DOID:0111374,selective pituitary thyroid hormone resistance,C1840364,,190160;145650,MONDO:0007784,selective pituitary resistance to thyroid hormone,
+BMGC_DS10506,BMG_DS038513,764957003,King Denborough syndrome,,,,,DOID:0080990,King Denborough syndrome,C1840365,C536883,619542,MONDO:0020485,King-Denborough syndrome,King Denborough syndrome | King Denborough syndrome (disorder) | Koussef Nichols syndrome
+BMGC_DS10507,BMG_DS038514,,"Hyperthermia, Cutaneous, With Headaches And Nausea",,,,,,,C1840373,C564156,145590,MONDO:0007782,"hyperthermia, cutaneous, with headaches and nausea",
+BMGC_DS10508,BMG_DS038515,,Hypertaurinuric Cardiomyopathy,,,,,,,C1840385,C564157,,,,
+BMGC_DS10509,BMG_DS038516,,Familial hypersensitivity pneumonitis,,,,,,,C1840386,C536846,145300,MONDO:0007776,"hypersensitivity pneumonitis, familial",
+BMGC_DS10510,BMG_DS038519,,"Pseudohypoaldosteronism, Type IIa",,,,,,,C1840389,C564160,145260,MONDO:0007772,pseudohypoaldosteronism type 2A,
+BMGC_DS10511,BMG_DS038520,,"Pseudohypoaldosteronism, Type IIb",,,,,,,C1840390,C564161,614491,MONDO:0013777,pseudohypoaldosteronism type 2B,
+BMGC_DS10512,BMG_DS038521,,"Pseudohypoaldosteronism, Type IIc",,,,,,,C1840391,C564162,614492,MONDO:0013778,pseudohypoaldosteronism type 2C,
+BMGC_DS10513,BMG_DS038522,,,,,,,,,C1840392,,145250,MONDO:0007771,"hyperpigmentation with or without hypopigmentation, familial progressive",
+BMGC_DS10514,BMG_DS038523,,Hyperpigmentation of Fuldauer and Kuijpers,,,,,,,C1840393,C564164,145200,MONDO:0007770,hyperpigmentation of Fuldauer and Kuijpers,
+BMGC_DS10515,BMG_DS038525,,HYPERPARATHYROIDISM 1,,,,,,,C1840402,,145000;607393,MONDO:0007767,hyperparathyroidism 1,
+BMGC_DS10516,BMG_DS038527,,Hyperostosis Cranialis Interna,,,,,,,C1840404,C564168,144755,MONDO:0007765,hyperostosis cranialis interna,
+BMGC_DS10517,BMG_DS038528,,"Hyperlipoproteinemia, Type II, and Deafness",,,,,,,C1840425,C564170,144300,MONDO:0007760,"hyperlipoproteinemia, type II, and deafness",
+BMGC_DS10518,BMG_DS038529,,"Palmoplantar Keratoderma, Epidermolytic, with Knuckle Pads",,,,,,,C1840427,C564171,,,,
+BMGC_DS10519,BMG_DS038532,,,,,,,DOID:0111371,isolated hyperchlorhidrosis,C1840437,,143860,MONDO:0007747,isolated hyperchlorhidrosis,
+BMGC_DS10520,BMG_DS038533,,"Orthostatic Hypotensive Disorder, Streeten Type",,,,,,,C1840438,C564174,143850,MONDO:0007746,"orthostatic hypotensive disorder, Streeten type",
+BMGC_DS10521,BMG_DS038534,,"MULTICYSTIC RENAL DYSPLASIA, BILATERAL",,,,,DOID:0080207,CAKUT2,C1840451,,143400,MONDO:0019982,bilateral multicystic dysplastic kidney,
+BMGC_DS10522,BMG_DS038535,,Hyaloideoretinal degeneration of Wagner,,,,,,,C1840452,C536075,143200,MONDO:0007740,Wagner disease,
+BMGC_DS10523,BMG_DS038536,,"Horner Syndrome, Congenital",,,,,,,C1840475,C564178,143000,MONDO:0007735,congenital Horner syndrome,
+BMGC_DS10524,BMG_DS038537,,Holoprosencephaly 4,,,,,DOID:0110880,holoprosencephaly 4,C1840528,C564180,142946,MONDO:0007734,holoprosencephaly 4,
+BMGC_DS10525,BMG_DS038538,,HOLOPROSENCEPHALY 3,,,,,,,C1840529,,142945;600725,MONDO:0007733,holoprosencephaly 3,
+BMGC_DS10526,BMG_DS038540,,"Hidradenitis suppurativa, familial",,,,,,,C1840560,C538118,,MONDO:0024516,familial acne inversa,
+BMGC_DS10527,BMG_DS038541,,"HIP DYSPLASIA, BEUKES TYPE",,,,,DOID:0111367,Beukes hip dysplasia,C1840572,,142669;611482,MONDO:0007726,"hip dysplasia, Beukes type",
+BMGC_DS10528,BMG_DS038542,,"Histiocytosis, Progressive Mucinous",,,,,,,C1840586,C564186,142630,MONDO:0007725,hereditary progressive mucinous histiocytosis,
+BMGC_DS10529,BMG_DS038543,,,,,,,,,C1840643,,142340,MONDO:0007719,diaphragmatic hernia 1,
+BMGC_DS10530,BMG_DS038544,,"Hepatic Adenomas, Familial",,,,,,,C1840646,C564190,142330,MONDO:0007718,"hepatic adenomas, familial",
+BMGC_DS10531,BMG_DS038545,,HEMOGLOBIN--VARIANTS FOR WHICH THE CHAIN CARRYING THE MUTATION IS UNKNOWN OR UNCERTAIN,,,,,,,C1840647,,142309,MONDO:0007717,hemoglobin--variants for which the chain carrying the mutation 1S unknown or uncertain,
+BMGC_DS10532,BMG_DS038548,,"Methemoglobinemia, Alpha-Globin Type",,,,,,,C1841414,C564194,,,,
+BMGC_DS10533,BMG_DS038552,,"Hemifacial Spasm, Familial",,,,,,,C1841639,C564198,141405,MONDO:0007713,clonic hemifacial spasm,
+BMGC_DS10534,BMG_DS038553,,Hemifacial Hyperplasia With Strabismus,,,,,,,C1841640,C564199,141350,MONDO:0007711,Bencze syndrome,
+BMGC_DS10535,BMG_DS038554,,Heme Oxygenase 1 Deficiency,,,,,,,C1841651,C564200,614034,MONDO:0013536,heme oxygenase 1 deficiency,
+BMGC_DS10536,BMG_DS038555,,,,,,,,,C1841654,,140900,MONDO:0007707,hemangiomas of small intestine,
+BMGC_DS10537,BMG_DS038556,,"Heart-hand syndrome, Spanish type",,,,,,,C1841657,C535853,140450,MONDO:0007702,heart-hand syndrome type 3,
+BMGC_DS10538,BMG_DS038557,,"Progressive Familial Heart Block, Type II",,,,,DOID:0111075,progressive familial heart block type II,C1841658,C564202,140400,MONDO:0007701,progressive familial heart block type II,
+BMGC_DS10539,BMG_DS038559,,Hand foot uterus syndrome,,,,,,,C1841679,C535627,140000,MONDO:0007698,hand-foot-genital syndrome,
+BMGC_DS10540,BMG_DS038563,,,,,,,,,C1841694,,139650,MONDO:0007695,hairy palms and soles,
+BMGC_DS10541,BMG_DS038564,,,,,,,,,C1841695,,139630,MONDO:0007694,hairy nose tip,
+BMGC_DS10542,BMG_DS038566,,ACHROMATOPSIA 4,,,,,,,C1841721,,139340;613856,MONDO:0013465,achromatopsia 4,
+BMGC_DS10543,BMG_DS038567,,"Prolonged Bleeding Time, Brachydactyly, and Mental Retardation",,,,,,,C1841727,C564207,,,,
+BMGC_DS10544,BMG_DS038571,723827003,Grant syndrome,,,,,,,C1841835,C537293,138930,MONDO:0007683,Grant syndrome,Grant syndrome | Grant syndrome (disorder)
+BMGC_DS10545,BMG_DS038578,,Glucocorticoid Receptor Deficiency,,,,,,,C1841972,C564221,615962,MONDO:0014421,glucocorticoid resistance,
+BMGC_DS10546,BMG_DS038579,,"Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance",,,,,,,C1841973,C564221,,,,
+BMGC_DS10547,BMG_DS038580,,GLOMUVENOUS MALFORMATIONS,,,,,,,C1841984,,138000;601749,MONDO:0007672,glomuvenous malformation,
+BMGC_DS10548,BMG_DS038583,,Globulin Anomaly involving Beta (2A)-Globulin,,,,,,,C1842009,C564229,137900,MONDO:0007668,globulin anomaly involving beta (2A)-globulin,
+BMGC_DS10549,BMG_DS038584,,Glaucoma and Sleep Apnea,,,,,,,C1842025,C564232,137763,MONDO:0007666,glaucoma-sleep apnea syndrome,
+BMGC_DS10550,BMG_DS038585,,"GLAUCOMA 1, OPEN ANGLE, E",,,,,,,C1842026,,602432;137760,,,
+BMGC_DS10551,BMG_DS038586,,"GLAUCOMA 1, OPEN ANGLE, A",,,,,DOID:1068,juvenile glaucoma,C1842028,,137750;601652,MONDO:0007664,"glaucoma 1, open angle, A",
+BMGC_DS10552,BMG_DS038588,,"IRIDOGONIODYSGENESIS, TYPE 2",,,,,DOID:0080609,anterior segment dysgenesis 4,C1842031,,137600,MONDO:0007662,anterior segment dysgenesis 4,
+BMGC_DS10553,BMG_DS038589,,Giant Platelet Syndrome with Thrombocytopenia,,,,,,,C1842035,C564237,137560,MONDO:0007659,obsolete giant platelet syndrome with thrombocytopenia,
+BMGC_DS10554,BMG_DS038590,,,,,,,DOID:0111359,large congenital melanocytic nevus,C1842036,,137550,MONDO:0044792,large congenital melanocytic nevus,
+BMGC_DS10555,BMG_DS038591,,GIANT NEUTROPHIL LEUKOCYTES,,,,,,,C1842039,,137500,MONDO:0007657,giant neutrophil leukocytes,
+BMGC_DS10556,BMG_DS038596,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F",,,,,,,C1842062,,608423,MONDO:0012034,autosomal dominant limb-girdle muscular dystrophy type 1F,
+BMGC_DS10557,BMG_DS038597,,,,,,,DOID:0050335,bradyopsia,C1842073,,,MONDO:0012033,bradyopsia,
+BMGC_DS10558,BMG_DS038599,,Platelet Glycoprotein IV Deficiency,,,,,,,C1842090,C564245,608404,MONDO:0012031,platelet-type bleeding disorder 10,
+BMGC_DS10559,BMG_DS038600,,"Deafness, Autosomal Dominant 43",,,,,,,C1842108,C564246,608394,MONDO:0012030,autosomal dominant nonsyndromic hearing loss 43,
+BMGC_DS10560,BMG_DS038601,,"Microcephaly, Primary Autosomal Recessive, 6",,,,,,,C1842109,C564247,608393,MONDO:0012029,"microcephaly 6, primary, autosomal recessive",
+BMGC_DS10561,BMG_DS038604,,Branchiootic Syndrome 3,,,,,,,C1842124,C564248,608389,MONDO:0012025,branchiootic syndrome 3,
+BMGC_DS10562,BMG_DS038605,,Retinitis Pigmentosa 26,,,,,DOID:0110368,retinitis pigmentosa 26,C1842127,C564249,608380,MONDO:0012024,retinitis pigmentosa 26,
+BMGC_DS10563,BMG_DS038606,,"Deafness, Autosomal Dominant 49",,,,,,,C1842136,C564250,608372,MONDO:0012023,autosomal dominant nonsyndromic hearing loss 49,
+BMGC_DS10564,BMG_DS038607,,Orofacial Cleft 4,,,,,DOID:0080398,orofacial cleft 4,C1842143,C564251,608371,MONDO:0012022,orofacial cleft 4,
+BMGC_DS10565,BMG_DS038608,,,,,,,DOID:0112282,spondyloepiphyseal dysplasia Kimberley type,C1842149,,608361,MONDO:0012019,"spondyloepiphyseal dysplasia, Kimberley type",
+BMGC_DS10566,BMG_DS038609,699267007,Myosin storage myopathy,,,,,,,C1842160,,181430;608358,MONDO:0008409,"congenital myopathy 7A, myosin storage, autosomal dominant",Myosin storage myopathy (disorder) | Myosin storage myopathy | Hyaline body myopathy
+BMGC_DS10567,BMG_DS038610,,Capillary Malformation-Arteriovenous Malformation,,,,,,,C1842180,C564254,,MONDO:0012016,capillary malformation-arteriovenous malformation syndrome,
+BMGC_DS10568,BMG_DS038611,,"Nystagmus 3, congenital, autosomal dominant",,,,,,,C1842186,C537855,608345,MONDO:0012015,"nystagmus 3, congenital, autosomal dominant",
+BMGC_DS10569,BMG_DS038612,,"Charcot-Marie-Tooth Disease, Recessive Intermediate A",,,,,DOID:0110201,Charcot-Marie-Tooth disease recessive intermediate A,C1842197,C564256,608340,MONDO:0012014,Charcot-Marie-Tooth disease recessive intermediate A,
+BMGC_DS10570,BMG_DS038613,,"Charcot-Marie-Tooth Disease, Dominant Intermediate C",,,,,DOID:0110199,Charcot-Marie-Tooth disease dominant intermediate C,C1842237,C564257,608323,MONDO:0012012,Charcot-Marie-Tooth disease dominant intermediate C,
+BMGC_DS10571,BMG_DS038614,,"CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1",,,,,,,C1842247,,608320,MONDO:0012011,"coronary artery disease, autosomal dominant, 1",
+BMGC_DS10572,BMG_DS038621,,"Deafness, Autosomal Recessive 39",,,,,,,C1842342,C564265,608265,MONDO:0012003,autosomal recessive nonsyndromic hearing loss 39,
+BMGC_DS10573,BMG_DS038622,,"Deafness, Autosomal Recessive 40",,,,,,,C1842345,C564266,608264,MONDO:0012002,autosomal recessive nonsyndromic hearing loss 40,
+BMGC_DS10574,BMG_DS038623,,"Mandibulofacial Dysostosis with Ptosis, Autosomal Dominant",,,,,,,C1842349,C564267,608257,MONDO:0012001,"mandibulofacial dysostosis with ptosis, autosomal dominant",
+BMGC_DS10575,BMG_DS038624,,OTOSCLEROSIS 3,,,,,DOID:0060922,otosclerosis 3,C1842353,,608244,MONDO:0011999,otosclerosis 3,
+BMGC_DS10576,BMG_DS038625,,"Slowed Nerve Conduction Velocity, Autosomal Dominant",,,,,,,C1842357,C564269,608236,MONDO:0011998,autosomal dominant slowed nerve conduction velocity,
+BMGC_DS10577,BMG_DS038626,,HERMANSKY-PUDLAK SYNDROME 2,,,,,,,C1842362,,603401;608233,MONDO:0011997,Hermansky-Pudlak syndrome 2,
+BMGC_DS10578,BMG_DS038627,,"Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation",,,,,,,C1842363,C564271,608227,MONDO:0011995,cataract - congenital heart disease - neural tube defect syndrome,
+BMGC_DS10579,BMG_DS038628,,"Deafness, Autosomal Dominant 41",,,,,,,C1842371,C564272,608224,MONDO:0011994,autosomal dominant nonsyndromic hearing loss 41,
+BMGC_DS10580,BMG_DS038630,,"DEAFNESS, AUTOSOMAL RECESSIVE 38",,,,,,,C1842381,,608219,MONDO:0011991,autosomal recessive nonsyndromic hearing loss 38,
+BMGC_DS10581,BMG_DS038631,,"Epilepsy, Benign Neonatal, 3",,,,,,,C1842382,C564274,608217,MONDO:0011990,"seizures, benign familial neonatal, 3",
+BMGC_DS10582,BMG_DS038632,,Neutrophil Immunodeficiency Syndrome,,,,,DOID:0112064,immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis,C1842398,C564275,608203,MONDO:0011988,neutrophil immunodeficiency syndrome,
+BMGC_DS10583,BMG_DS038633,,TROPICAL CALCIFIC PANCREATITIS,,,,,,,C1842402,,167790;608189,MONDO:0011986,tropical pancreatitis,
+BMGC_DS10584,BMG_DS038634,,"IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 4",,,,,DOID:0060760,immunodeficiency with hyper-IgM type 4,C1842413,,608184,MONDO:0011985,hyper-IgM syndrome type 4,
+BMGC_DS10585,BMG_DS038635,,Synpolydactyly 2,,,,,,,C1842422,C564278,608180,MONDO:0011984,synpolydactyly type 2,
+BMGC_DS10586,BMG_DS038637,,,,,,,,,C1842444,,608175,MONDO:0011982,"autoimmune thyroid disease, susceptibility to, 3",
+BMGC_DS10587,BMG_DS038640,,CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL,,,,,,,C1842462,,114290;608160,,,
+BMGC_DS10588,BMG_DS038642,719664004,Nablus mask-like facial syndrome,,,,,,,C1842464,C536110,608156,MONDO:0011977,8q22.1 microdeletion syndrome,8q22.1 microdeletion syndrome (disorder) | 8q22.1 microdeletion syndrome | Monosomy 8q22.1 | Nablus mask-like facial syndrome
+BMGC_DS10589,BMG_DS038643,,"Lipodystrophy, Generalized, with Mental Retardation, Deafness, Short Stature, and Slender Bones",,,,,,,C1842465,C564283,608154,MONDO:0011976,lipodystrophy-intellectual disability-deafness syndrome,
+BMGC_DS10590,BMG_DS038645,,Retinitis Pigmentosa 7,,,,,DOID:0110383,retinitis pigmentosa 7,C1842475,C564284,608133,MONDO:0011974,retinitis pigmentosa 7,
+BMGC_DS10591,BMG_DS038646,,"Zinc Deficiency, Neonatal, due to Low Breast Milk Zinc",,,,,,,C1842486,C564286,608118,MONDO:0011973,"zinc deficiency, transient neonatal",
+BMGC_DS10592,BMG_DS038647,,"Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp",,,,,,,C1842531,C535499,608105,MONDO:0011970,rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome,
+BMGC_DS10593,BMG_DS038648,724072002,Dystonia 18,,,,,DOID:0090045,glucose transporter type 1 deficiency syndrome 2,C1842534,C564288,612126,MONDO:0012805,childhood onset GLUT1 deficiency syndrome 2,Paroxysmal exertion-induced dyskinesia (disorder) | Paroxysmal exertion-induced dyskinesia | Dystonia 18
+BMGC_DS10594,BMG_DS038649,,Limb-girdle muscle atrophy,,,,,,,C1842552,,MTHU002477,,,
+BMGC_DS10595,BMG_DS038651,,"Heterotopia, Periventricular, Autosomal Recessive",,,,,,,C1842563,C564292,608097,MONDO:0011966,"periventricular heterotopia with microcephaly, autosomal recessive",
+BMGC_DS10596,BMG_DS038653,,JOUBERT SYNDROME 2,,,,,,,C1842577,,608091;613277,MONDO:0011963,Joubert syndrome 2,
+BMGC_DS10597,BMG_DS038654,,"Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux",,,,,DOID:0070148,hereditary sensory neuropathy type 1B,C1842586,C564296,608088,MONDO:0011961,hereditary sensory and autonomic neuropathy type 1B,
+BMGC_DS10598,BMG_DS038655,,SCHIZOPHRENIA 11,,,,,DOID:0070087,schizophrenia 11,C1842605,,608078,MONDO:0011960,schizophrenia 11,
+BMGC_DS10599,BMG_DS038657,,,,,,,,,C1842632,,608049,MONDO:0011956,"autism, susceptibility to, 3",
+BMGC_DS10600,BMG_DS038662,,"Spinocerebellar ataxia, autosomal recessive 6",,,,,DOID:0111617,autosomal recessive spinocerebellar ataxia 6,C1842676,C537312,608029,MONDO:0011950,infantile-onset autosomal recessive nonprogressive cerebellar ataxia,
+BMGC_DS10601,BMG_DS038664,,Pontocerebellar Hypoplasia Type 3,,,,,DOID:0060272,pontocerebellar hypoplasia type 3,C1842687,C548072,608027,MONDO:0011948,pontocerebellar hypoplasia type 3,
+BMGC_DS10602,BMG_DS038665,721094006,Diaphanospondylodysostosis,,,,,,,C1842691,C564305,608022,MONDO:0011946,diaphanospondylodysostosis,Diaphanospondylodysostosis (disorder) | Diaphanospondylodysostosis
+BMGC_DS10603,BMG_DS038666,,"GAUCHER DISEASE, PERINATAL LETHAL",,,,,,,C1842704,,608013;606463,MONDO:0011945,Gaucher disease perinatal lethal,
+BMGC_DS10604,BMG_DS038671,,SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION,,,,,,,C1842763,,171640;271550;607944;607944,MONDO:0011939,Spondyloenchondrodysplasia with immune dysregulation,
+BMGC_DS10605,BMG_DS038672,,Atrial septal defect 2,,,,,,,C1842778,C538263,607941,MONDO:0011938,atrial septal defect 2,
+BMGC_DS10606,BMG_DS038673,,"Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like",,,,,DOID:0070523,peeling skin syndrome 4,C1842797,C564309,,,,
+BMGC_DS10607,BMG_DS038674,,RETINITIS PIGMENTOSA 30,,,,,,,C1842816,,607643;607921,MONDO:0011935,retinitis pigmentosa 30,
+BMGC_DS10608,BMG_DS038675,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii",,,,,DOID:0080561,congenital disorder of glycosylation Ii,C1842836,,607905;607906,MONDO:0011933,ALG2-congenital disorder of glycosylation,
+BMGC_DS10609,BMG_DS038676,,HYPOTRICHOSIS 6,,,,,DOID:0110703,hypotrichosis 6,C1842839,,607892;607903,MONDO:0011932,hypotrichosis 6,
+BMGC_DS10610,BMG_DS038677,,,,,,,,,C1842852,,607876,MONDO:0011930,"epilepsy, familial adult myoclonic, 2",
+BMGC_DS10611,BMG_DS038678,,Chromosome 1p36 Deletion Syndrome,,,,,DOID:0060410,chromosome 1p36 deletion syndrome,C1842870,C535362,607872,MONDO:0011929,chromosome 1p36 deletion syndrome,
+BMGC_DS10612,BMG_DS038679,,Caudal Duplication Anomaly,,,,,,,C1842884,C564315,607864,MONDO:0011928,caudal duplication,
+BMGC_DS10613,BMG_DS038681,,"Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency",,,,,,,C1842898,C564317,,,,
+BMGC_DS10614,BMG_DS038682,,Adult-Onset Vitelliform Macular Dystrophy,Vitelliform Macular Dystrophy,,,,DOID:0050661,vitelliform macular dystrophy,C1842914,D057826,,MONDO:0011979,adult-onset foveomacular vitelliform dystrophy,
+BMGC_DS10615,BMG_DS038684,,"Neutropenia, Nonimmune Chronic Idiopathic, Adult",,,,,,,C1842930,C564320,607847,MONDO:0011922,nonimmune chronic idiopathic neutropenia of adults,
+BMGC_DS10616,BMG_DS038685,,"AURAL ATRESIA, CONGENITAL",,,,,,,C1842937,,614427;607842,MONDO:0011921,"aural atresia, congenital",
+BMGC_DS10617,BMG_DS038686,,"Deafness, Autosomal Dominant 48",,,,,,,C1842939,C564322,607841,MONDO:0011920,autosomal dominant nonsyndromic hearing loss 48,
+BMGC_DS10618,BMG_DS038687,,,,,,,,,C1842979,,607836,MONDO:0011919,"autoimmune disease, susceptibility to, 1",
+BMGC_DS10619,BMG_DS038688,,,,,,,,,C1842982,,607832,MONDO:0011917,"focal segmental glomerulosclerosis 3, susceptibility to",
+BMGC_DS10620,BMG_DS038689,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K",,,,,,,C1842983,,607831,MONDO:0011916,Charcot-Marie-Tooth disease axonal type 2K,
+BMGC_DS10621,BMG_DS038690,,"Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k",,,,,,,C1842984,C564325,,MONDO:0020558,autosomal dominant Charcot-Marie-Tooth disease type 2K,
+BMGC_DS10622,BMG_DS038691,,"MITRAL VALVE PROLAPSE, MYXOMATOUS 2",,,,,,,C1843003,,607829,MONDO:0011915,"mitral valve prolapse, myxomatous 2",
+BMGC_DS10623,BMG_DS038692,,HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME,,,,,,,C1843004,,601618;607823,MONDO:0011914,hypotrichosis-lymphedema-telangiectasia syndrome,
+BMGC_DS10624,BMG_DS038693,,"Alzheimer disease, familial, type 3",,,,,,,C1843013,C536598,607822,MONDO:0011913,Alzheimer disease 3,
+BMGC_DS10625,BMG_DS038694,,"Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques",,,,,,,C1843014,C564329,,,,
+BMGC_DS10626,BMG_DS038695,,"Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia",,,,,,,C1843015,C564330,,,,
+BMGC_DS10627,BMG_DS038696,,"Deafness, Autosomal Recessive 37",,,,,,,C1843028,C564331,607821,MONDO:0011912,autosomal recessive nonsyndromic hearing loss 37,
+BMGC_DS10628,BMG_DS038697,,Craniolenticulosutural Dysplasia,,,,,DOID:0070307,craniolenticulosutural dysplasia,C1843042,C564332,607812,MONDO:0011911,craniolenticulosutural dysplasia,
+BMGC_DS10629,BMG_DS038698,,"Charcot-Marie-Tooth Disease, Dominant Intermediate D",,,,,DOID:0110200,Charcot-Marie-Tooth disease dominant intermediate D,C1843075,C564333,607791,MONDO:0011909,Charcot-Marie-Tooth disease dominant intermediate D,
+BMGC_DS10630,BMG_DS038699,,Acrocapitofemoral Dysplasia,,,,,DOID:0050604,acrocapitofemoral dysplasia,C1843096,C564334,607778,MONDO:0011907,acrocapitofemoral dysplasia,
+BMGC_DS10631,BMG_DS038700,,"Bile acid synthesis defect, congenital, 1",,,,,DOID:0111071,congenital bile acid synthesis defect 1,C1843116,C535442,607765,MONDO:0011906,congenital bile acid synthesis defect 1,
+BMGC_DS10632,BMG_DS038701,,"Hypercholanemia, Familial",,,,,,,C1843139,C564336,,MONDO:0100327,"hypercholanemia, familial",
+BMGC_DS10633,BMG_DS038702,,"SEIZURES, BENIGN FAMILIAL INFANTILE, 3",,,,,DOID:0081116,benign familial infantile seizures 3,C1843140,,182390;607745,MONDO:0011904,"seizures, benign familial infantile, 3",
+BMGC_DS10634,BMG_DS038704,,"Charcot-Marie-Tooth disease, Type 2J",,,,,,,C1843153,C535417,607736,MONDO:0011903,Charcot-Marie-Tooth disease type 2J,
+BMGC_DS10635,BMG_DS038705,,"Charcot-Marie-Tooth disease, demyelinating, Type 1F",,,,,,,C1843164,C537987,607734,MONDO:0011902,Charcot-Marie-Tooth disease type 1F,
+BMGC_DS10636,BMG_DS038706,,"Charcot-Marie-Tooth disease, Type 2H",,,,,,,C1843173,C535415,607731,MONDO:0011901,Charcot-Marie-Tooth disease axonal type 2H,
+BMGC_DS10637,BMG_DS038708,723444009,Noonan syndrome-like disorder with loose anagen hair,,,,,,,C1843181,,,MONDO:0011899,Noonan syndrome-like disorder with loose anagen hair,Noonan syndrome-like disorder with loose anagen hair (disorder) | Noonan syndrome-like disorder with loose anagen hair | Tosti syndrome
+BMGC_DS10638,BMG_DS038709,,"Charcot-Marie-Tooth disease, Type 4A, axonal form",,,,,,,C1843183,C539595,607706,MONDO:0011898,"Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive",
+BMGC_DS10639,BMG_DS038710,,Parkinson Disease 11,,,,,,,C1843211,C564345,,,,
+BMGC_DS10640,BMG_DS038711,,"Charcot-Marie-Tooth disease, Type 2E",,,,,,,C1843225,C537994,607684,MONDO:0011894,Charcot-Marie-Tooth disease type 2E,
+BMGC_DS10641,BMG_DS038714,,"Charcot-Marie-Tooth disease, Type 1D",,,,,DOID:0110150,Charcot-Marie-Tooth disease type 1D,C1843247,C537985,607678,MONDO:0011890,Charcot-Marie-Tooth disease type 1D,
+BMGC_DS10642,BMG_DS038715,,IRAK4 Deficiency,,,,,,,C1843256,C564352,607676,MONDO:0011888,immunodeficiency 67,
+BMGC_DS10643,BMG_DS038716,,"Cataract, Congenital, with Mental Impairment and Dentate Gyrus Atrophy",,,,,,,C1843257,C564353,607674,MONDO:0011887,"cataract, congenital, with mental impairment and dentate gyrus atrophy",
+BMGC_DS10644,BMG_DS038717,,,,,,,,,C1843264,,607671,MONDO:0011886,torsion dystonia 13,
+BMGC_DS10645,BMG_DS038724,,Skin Fragility-Woolly Hair Syndrome,,,,,,,C1843292,C564359,620415,MONDO:0957307,woolly hair-skin fragility syndrome,
+BMGC_DS10646,BMG_DS038725,,"CANDIDIASIS, FAMILIAL CHRONIC NAIL, WITH ICAM1 DEFICIENCY",,,,,,,C1843306,,607644,MONDO:0011880,"candidiasis, familial, 3",
+BMGC_DS10647,BMG_DS038726,,"Neuronopathy, Distal Hereditary Motor, Type Viib",,,,,,,C1843315,C564362,607641,MONDO:0011879,"neuronopathy, distal hereditary motor, type 7B",
+BMGC_DS10648,BMG_DS038727,,Van Buchem disease type 2,,,,,,,C1843323,C536527,,,,
+BMGC_DS10649,BMG_DS038728,,"OSTEOPETROSIS, AUTOSOMAL DOMINANT 1",,,,,DOID:0110937,autosomal dominant osteopetrosis 1,C1843330,,603506;607634,MONDO:0011877,autosomal dominant osteopetrosis 1,
+BMGC_DS10650,BMG_DS038729,,"ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS",,,,,,,C1843355,,603718;607626,MONDO:0011874,neonatal ichthyosis-sclerosing cholangitis syndrome,
+BMGC_DS10651,BMG_DS038730,,"NIEMANN-PICK DISEASE, TYPE C2",,,,,,,C1843366,,601015;607625,MONDO:0011873,"Niemann-Pick disease, type C2",
+BMGC_DS10652,BMG_DS038733,,"Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis",,,,,,,C1843463,C564367,,MONDO:0011870,annular epidermolytic ichthyosis,
+BMGC_DS10653,BMG_DS038735,,Lethal Congenital Contracture Syndrome 2,,,,,DOID:0060560,lethal congenital contracture syndrome 2,C1843478,C564369,607598,MONDO:0011868,lethal congenital contracture syndrome 2,
+BMGC_DS10654,BMG_DS038738,,"Pontocerebellar Hypoplasia, Type 1a",,,,,DOID:0112322,pontocerebellar hypoplasia type 1,C1843504,C548069,607596,MONDO:0011866,pontocerebellar hypoplasia type 1A,
+BMGC_DS10655,BMG_DS038742,,"Spastic Paraplegia 24, Autosomal Recessive",,,,,,,C1843569,C564375,607584,MONDO:0011862,hereditary spastic paraplegia 24,
+BMGC_DS10656,BMG_DS038743,,"LEPROSY, SUSCEPTIBILITY TO, 2",,,,,,,C1843632,,607572,MONDO:0011860,"leprosy, susceptibility to, 2",
+BMGC_DS10657,BMG_DS038744,,,,,,,,,C1843661,,607565,MONDO:0011858,"spastic paraplegia, ataxia, and intellectual disability",
+BMGC_DS10658,BMG_DS038745,,"Atrial fibrillation, familial 1",,,,,,,C1843687,C538261,608583,MONDO:0012066,"atrial fibrillation, familial, 1",
+BMGC_DS10659,BMG_DS038749,,,,,,,,,C1843758,,607539,MONDO:0011853,"Camptosynpolydactyly, complex",
+BMGC_DS10660,BMG_DS038750,,"TOENAIL DYSTROPHY, ISOLATED",,,,,DOID:0080086,nonsyndromic congenital nail disorder 8,C1843761,,607523,MONDO:0011852,nonsyndromic congenital nail disorder 8,
+BMGC_DS10661,BMG_DS038751,,,,,,,,,C1843765,,607516,MONDO:0011851,"migraine with or without aura, susceptibility to, 6",
+BMGC_DS10662,BMG_DS038753,,,,,,,,,C1843771,,607508,MONDO:0011850,"migraine with or without aura, susceptibility to, 5",
+BMGC_DS10663,BMG_DS038755,,,,,,,,,C1843773,,607501,MONDO:0011847,"migraine without aura, susceptibility to, 4",
+BMGC_DS10664,BMG_DS038756,,,,,,,,,C1843776,,607499,MONDO:0011846,"bulimia nervosa, susceptibility to, 1",
+BMGC_DS10665,BMG_DS038757,,,,,,,,,C1843782,,607498,MONDO:0011845,"migraine with or without aura, susceptibility to, 3",
+BMGC_DS10666,BMG_DS038758,,"DYSTONIA 15, MYOCLONIC",,,,,DOID:0090035,myoclonic dystonia 15,C1843786,,607488,MONDO:0011844,myoclonic dystonia 15,
+BMGC_DS10667,BMG_DS038759,,"FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED",,,,,,,C1843792,,607485,MONDO:0011842,GRN-related frontotemporal lobar degeneration with Tdp43 inclusions,
+BMGC_DS10668,BMG_DS038760,703522009,Biotin-thiamine-responsive basal ganglia disease,,,,,,,C1843807,,607483,MONDO:0011841,biotin-responsive basal ganglia disease,Thiamine transporter-2 deficiency | Thiamine metabolism dysfunction syndrome 2 | Biotin-thiamine-responsive basal ganglia disease (disorder) | Biotin-responsive basal ganglia disease | Biotin-thiamine-responsive basal ganglia disease
+BMGC_DS10669,BMG_DS038761,,"CARDIOMYOPATHY, DILATED, 1M",,,,,,,C1843808,,607482;600824,MONDO:0011840,dilated cardiomyopathy 1M,
+BMGC_DS10670,BMG_DS038762,,Newfoundland Rod-Cone Dystrophy,,,,,,,C1843815,C564391,607476,MONDO:0011839,Newfoundland cone-rod dystrophy,
+BMGC_DS10671,BMG_DS038763,,Bothnia Retinal Dystrophy,,,,,DOID:0050683,Bothnia retinal dystrophy,C1843816,C564392,607475,MONDO:0011838,Bothnia retinal dystrophy,
+BMGC_DS10672,BMG_DS038764,,"VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2",,,,,,,C1843832,,607473;608547,MONDO:0011837,"vitamin K-dependent clotting factors, combined deficiency of, type 2",
+BMGC_DS10673,BMG_DS038765,,"Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis",,,,,DOID:0111276,"sensory ataxic neuropathy, dysarthria, and ophthalmoparesis",C1843851,C537583,613832;607459,MONDO:0011835,"sensory ataxic neuropathy, dysarthria, and ophthalmoparesis",
+BMGC_DS10674,BMG_DS038766,,SPINOCEREBELLAR ATAXIA WITH EPILEPSY,,,,,,,C1843852,,174763;607459,MONDO:0016809,spinocerebellar ataxia with epilepsy,
+BMGC_DS10675,BMG_DS038767,,SPINOCEREBELLAR ATAXIA 18,,,,,DOID:0050969,spinocerebellar ataxia type 18,C1843884,,607458,MONDO:0011834,spinocerebellar ataxia type 18,
+BMGC_DS10676,BMG_DS038768,,GIL BLOOD GROUP,,,,,,,C1843889,,600170;607457,,,
+BMGC_DS10677,BMG_DS038769,,SPINOCEREBELLAR ATAXIA 21,,,,,DOID:0050972,spinocerebellar ataxia type 21,C1843891,,607454;616101,MONDO:0011833,spinocerebellar ataxia type 21,
+BMGC_DS10678,BMG_DS038770,,"Deafness, Autosomal Dominant 44",,,,,,,C1843895,C564399,607453,MONDO:0011832,autosomal dominant nonsyndromic hearing loss 44,
+BMGC_DS10679,BMG_DS038771,,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 8",,,,,,,C1843896,C564400,607450,MONDO:0011831,arrhythmogenic right ventricular dysplasia 8,
+BMGC_DS10680,BMG_DS038772,,,,,,,,,C1843920,,,MONDO:0018151,coenzyme Q10 deficiency,
+BMGC_DS10681,BMG_DS038773,,,,,,,,,C1843942,,607417,MONDO:0011828,"intellectual disability, autosomal recessive 2",
+BMGC_DS10682,BMG_DS038774,,"Hypouricemia, Familial Renal, due to Tubular Hypersecretion",,,,,,,C1843972,C564405,307830,MONDO:0010620,"hypouricemia, familial renal, due to tubular hypersecretion",
+BMGC_DS10683,BMG_DS038775,,"Hypogonadism, Male, With Mental Retardation And Skeletal Anomalies",,,,,,,C1843994,C564406,307500,MONDO:0010617,male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome,
+BMGC_DS10684,BMG_DS038778,,"Hydrocephalus, X-Linked, with Congenital Idiopathic Intestinal Pseudoobstruction",,,,,,,C1844006,C564408,,,,
+BMGC_DS10685,BMG_DS038779,,Holoprosencephaly with Fetal Akinesia-Hypokinesia Sequence,,,,,,,C1844016,C564409,306990,MONDO:0010610,holoprosencephaly-hypokinesia-congenital contractures syndrome,
+BMGC_DS10686,BMG_DS038780,,Hirschsprung disease type d brachydactyly,,,,,,,C1844017,C538319,306980,MONDO:0016294,Hirschsprung disease-type D brachydactyly syndrome,
+BMGC_DS10687,BMG_DS038781,,Hhhh Syndrome,,,,,,,C1844019,C564411,306960,MONDO:0010608,Hhhh syndrome,
+BMGC_DS10688,BMG_DS038782,,"HETEROTAXY, VISCERAL, 1, X-LINKED",,,,,,,C1844020,,300265;306955,MONDO:0010607,"heterotaxy, visceral, 1, X-linked",
+BMGC_DS10689,BMG_DS038783,,,,,,,,,C1844025,,306950,MONDO:0010606,"hernia, anterior diaphragmatic",
+BMGC_DS10690,BMG_DS038784,,,,,,,,,C1844026,,306930,MONDO:0010605,hemopoietic proliferation,
+BMGC_DS10691,BMG_DS038787,,"Granulomatous Disease, Chronic, X-Linked","Granulomatous Disease, Chronic",,,,,,C1844376,D006105,306400;138990,MONDO:0010600,"granulomatous disease, chronic, X-linked",
+BMGC_DS10692,BMG_DS038789,,"Granulomas, congenital cerebral",,,,,,,C1844406,C537294,306300,MONDO:0010599,"granulomas, congenital cerebral",
+BMGC_DS10693,BMG_DS038792,,"Membranoproliferative Glomerulonephritis, X-Linked",,,,,,,C1844501,C564423,305800,MONDO:0010596,"membranoproliferative glomerulonephritis, X-linked",
+BMGC_DS10694,BMG_DS038793,,Fingerprint Body Myopathy,,,,,,,C1844560,C564425,305550,MONDO:0010591,fingerprint body myopathy,
+BMGC_DS10695,BMG_DS038795,,"Exudative Vitreoretinopathy, Familial, X-Linked Recessive",,,,,,,C1844579,C564428,305390,MONDO:0010588,"exudative vitreoretinopathy 2, X-linked",
+BMGC_DS10696,BMG_DS038798,,X-linked Dyggve-Melchior-Clausen syndrome,,,,,,,C1844654,C535726,304950,MONDO:0010583,"Dyggve-Melchior-Clausen syndrome, X-linked",
+BMGC_DS10697,BMG_DS038799,,Dermoids of cornea,,,,,,,C1844671,C535376,304730,MONDO:0010579,X-linked corneal dermoid,
+BMGC_DS10698,BMG_DS038801,,"Deafness, X-Linked 1",,,,,,,C1844677,C564433,304500,MONDO:0010577,"hearing loss, X-linked 1",
+BMGC_DS10699,BMG_DS038802,,Progressive hearing loss stapes fixation,,,,,,,C1844678,C536424,304400,MONDO:0010576,X-linked mixed hearing loss with perilymphatic gusher,
+BMGC_DS10700,BMG_DS038804,,"OTOPALATODIGITAL SYNDROME, TYPE II",,,,,DOID:0111784,otopalatodigital syndrome type 2,C1844696,,300017;304120,MONDO:0010571,otopalatodigital syndrome type 2,
+BMGC_DS10701,BMG_DS038806,,"CONE-ROD DYSTROPHY, X-LINKED, 1",,,,,DOID:0111008,X-linked cone-rod dystrophy 1,C1844776,,304020;312610,MONDO:0010566,X-linked cone-rod dystrophy 1,
+BMGC_DS10702,BMG_DS038807,,"CONE DYSTROPHY, X-LINKED, 1",,,,,,,C1844777,,312610,MONDO:0800320,"cone dystrophy 1, X-linked",
+BMGC_DS10703,BMG_DS038808,,"CLEFT PALATE, X-LINKED",,,,,,,C1844830,,300307;303400,MONDO:0010560,"cleft palate with or without ankyloglossia, X-linked",
+BMGC_DS10704,BMG_DS038809,,Cleft Palate with Ankyloglossia,,,,,,,C1844831,C564442,,,,
+BMGC_DS10705,BMG_DS038810,717761005,Ayazi syndrome,,,,,,,C1844836,C537793,,,,Choroideremia with deafness and obesity syndrome (disorder) | Choroideremia with deafness and obesity syndrome | Choroideraemia with deafness and obesity syndrome | Ayazi syndrome | Xq21 microdeletion syndrome
+BMGC_DS10706,BMG_DS038811,,Brachytelephalangic Chondrodysplasia Punctata,,,,,,,C1844853,C000705207,602497,MONDO:0011238,"chondrodysplasia punctata, brachytelephalangic, autosomal",
+BMGC_DS10707,BMG_DS038812,718574003,Abruzzo Erickson syndrome,,,,,DOID:0111826,Abruzzo-Erickson syndrome,C1844862,C535559,302905,MONDO:0010554,Abruzzo-Erickson syndrome,Abruzzo Erickson syndrome | CHARGE-like syndrome | Cleft palate with coloboma of eye and deafness syndrome (disorder) | Cleft palate with coloboma of eye and deafness syndrome
+BMGC_DS10708,BMG_DS038814,,Charcot Marie Tooth type 1 aplasia cutis congenita,,,,,,,C1844864,C538077,302803,MONDO:0010552,"Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia cutis congenita",
+BMGC_DS10709,BMG_DS038815,,"Charcot-Marie-Tooth disease, X-linked recessive, 3",,,,,DOID:0110211,Charcot-Marie-Tooth disease X-linked recessive 3,C1844865,C535303,302802,MONDO:0010551,Charcot-Marie-Tooth disease X-linked recessive 3,
+BMGC_DS10710,BMG_DS038816,,"Charcot-Marie-Tooth disease, X-linked recessive, 2",,,,,DOID:0110208,Charcot-Marie-Tooth disease X-linked recessive 2,C1844873,C535302,302801,MONDO:0010550,Charcot-Marie-Tooth disease X-linked recessive 2,
+BMGC_DS10711,BMG_DS038817,,"Cerebral Sclerosis, Diffuse, Scholz Type",,,,,,,C1844884,C564449,302700,MONDO:0060456,"cerebral sclerosis, diffuse, scholz type",
+BMGC_DS10712,BMG_DS038818,,"SPINOCEREBELLAR ATAXIA, X-LINKED 2",,,,,DOID:0111830,X-linked spinocerebellar ataxia 2,C1844885,,302600,MONDO:0010548,"spinocerebellar ataxia, X-linked 2",
+BMGC_DS10713,BMG_DS038819,,,,,,,,,C1844886,,302400,MONDO:0010546,"central incisors, absence of",
+BMGC_DS10714,BMG_DS038820,722383001,Catel Manzke syndrome,,,,,DOID:0081122,Catel Manzke syndrome,C1844887,C535347,302380;616145,MONDO:0014507,Catel-Manzke syndrome,Catel Manzke syndrome (disorder) | Catel Manzke syndrome | Micrognathia digital syndrome | Palatodigital syndrome Catel-Manzke type
+BMGC_DS10715,BMG_DS038823,,Branchial arch syndrome X-linked,,,,,,,C1844918,C537102,301950,MONDO:0010539,X-linked mandibulofacial dysostosis,
+BMGC_DS10716,BMG_DS038826,,"Arthrogryposis multiplex congenita, distal, X-linked",,,,,DOID:0111827,X-linked spinal muscular atrophy 2,C1844934,C535380,301830,MONDO:0010532,infantile-onset X-linked spinal muscular atrophy,
+BMGC_DS10717,BMG_DS038829,717222003,Microphthalmia with ankyloblepharon and intellectual disability syndrome,,,,,DOID:0111799,syndromic microphthalmia 1,C1844948,,,,,Microphthalmia with ankyloblepharon and intellectual disability syndrome (disorder) | Microphthalmia with ankyloblepharon and intellectual disability syndrome | Syndromic microphthalmia type 4
+BMGC_DS10718,BMG_DS038830,,Neural tube defects X-linked,,,,,,,C1845026,C536410,301410,MONDO:0010525,"neural tube defects, X-linked",
+BMGC_DS10719,BMG_DS038832,,"ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA",,,,,DOID:0050554,X-linked sideroblastic anemia with ataxia,C1845028,,301310,MONDO:0010524,X-linked sideroblastic anemia with ataxia,
+BMGC_DS10720,BMG_DS038833,,,,,,,DOID:0111834,X-linked reticulate pigmentary disorder,C1845050,,301220,MONDO:0010523,X-linked reticulate pigmentary disorder,
+BMGC_DS10721,BMG_DS038834,,"AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2",,,,,,,C1845051,,301201,MONDO:0010522,X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2,
+BMGC_DS10722,BMG_DS038835,,"AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1",,,,,,,C1845052,,301200,,,
+BMGC_DS10723,BMG_DS038836,,"Amelogenesis Imperfecta, Hypomaturation Type, with Snow-Capped Teeth",,,,,,,C1845053,C564463,301200,MONDO:0010521,amelogenesis imperfecta type 1E,
+BMGC_DS10724,BMG_DS038837,715342005,Alpha thalassemia X-linked intellectual disability syndrome,,,,,,,C1845055,,301040,MONDO:0010519,alpha thalassemia-X-linked intellectual disability syndrome,Alpha thalassemia X-linked intellectual disability syndrome (disorder) | Alpha thalassemia X-linked intellectual disability syndrome | Alpha thalassaemia X-linked intellectual disability syndrome | Alpha thalassemia X-linked intellectual deficit | Alpha thalassaemia X-linked intellectual deficit
+BMGC_DS10725,BMG_DS038838,,ALBINISM-DEAFNESS SYNDROME,,,,,,,C1845068,,300700,MONDO:0010403,albinism-hearing loss syndrome,
+BMGC_DS10726,BMG_DS038839,722054007,Ocular albinism with late-onset sensorineural deafness,,,,,,,C1845069,,300650,MONDO:0010390,ocular albinism with late-onset sensorineural deafness,Ocular albinism with late-onset sensorineural deafness (disorder) | Ocular albinism with late-onset sensorineural deafness
+BMGC_DS10727,BMG_DS038840,,"Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked",,,,,,,C1845070,C564467,300643,MONDO:0010388,"rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked",
+BMGC_DS10728,BMG_DS038841,,"Invasive Pneumococcal Disease, Recurrent Isolated, 2",,,,,,,C1845073,C564468,,,,
+BMGC_DS10729,BMG_DS038842,,"Lymphoproliferative Syndrome, X-Linked, 2",,,,,,,C1845076,C564469,300635,MONDO:0010385,X-linked lymphoproliferative disease due to XIAP deficiency,
+BMGC_DS10730,BMG_DS038843,,"Cataracts, ataxia, short stature, and mental retardation",,,,,,,C1845094,C535345,300619,MONDO:0010380,"cataract, ataxia, short stature, and intellectual disability",
+BMGC_DS10731,BMG_DS038844,,"Deafness, X-Linked 5",,,,,,,C1845095,C564472,,,,
+BMGC_DS10732,BMG_DS038846,,Hyperekplexia and Epilepsy,,,,,,,C1845102,C564474,300607,MONDO:0010375,"developmental and epileptic encephalopathy, 8",
+BMGC_DS10733,BMG_DS038847,,Retinitis Pigmentosa 34,,,,,DOID:0110417,retinitis pigmentosa 34,C1845104,C564475,300605,MONDO:0010374,retinitis pigmentosa 34,
+BMGC_DS10734,BMG_DS038848,,Premature Ovarian Failure 2b,,,,,,,C1845105,C564476,300604,MONDO:0010373,premature ovarian failure 2B,
+BMGC_DS10735,BMG_DS038849,,"Nystagmus 5, Infantile Periodic Alternating",,,,,,,C1845116,C564478,300589,MONDO:0010369,"nystagmus 5, congenital, X-linked",
+BMGC_DS10736,BMG_DS038851,,,,,,,,,C1845118,,300582,MONDO:0010367,SHOX-related short stature,
+BMGC_DS10737,BMG_DS038852,,Fg Syndrome 5,,,,,,,C1845119,C564480,300581,MONDO:0010366,FG syndrome 5,
+BMGC_DS10738,BMG_DS038853,,Chromosome Xp11.3 Deletion Syndrome,,,,,,,C1845136,C564481,300578,MONDO:0010364,X-linked intellectual disability-retinitis pigmentosa syndrome,
+BMGC_DS10739,BMG_DS038854,,,,,,,,,C1845142,,300577,MONDO:0010363,"intellectual disability, X-linked 91",
+BMGC_DS10740,BMG_DS038855,,,,,,,,,C1845144,,300851,MONDO:0010453,"intellectual disability, X-linked 92",
+BMGC_DS10741,BMG_DS038856,,,,,,,,,C1845146,,615465,MONDO:0014196,Hartsfield-Bixler-Demyer syndrome,
+BMGC_DS10742,BMG_DS038857,,"Glycogen Storage Disease, Type IXD",,,,,,,C1845151,C564485,300559,MONDO:0010362,glycogen storage disease IXd,
+BMGC_DS10743,BMG_DS038859,,Dent Disease 2,,,,,DOID:0081454,Dent disease 2,C1845167,C564487,300555,MONDO:0010359,Dent disease type 2,
+BMGC_DS10744,BMG_DS038860,,"Hypophosphatemic Rickets, X-Linked Recessive",Familial Hypophosphatemic Rickets,,,,DOID:0050445,X-linked dominant hypophosphatemic rickets,C1845168,D053098,300554,MONDO:0010358,"hypophosphatemic rickets, X-linked recessive",
+BMGC_DS10745,BMG_DS038861,,Nephrogenic Syndrome of Inappropriate Antidiuresis,,,,,DOID:0112121,nephrogenic syndrome of inappropriate antidiuresis,C1845202,C564491,300539,MONDO:0010356,nephrogenic syndrome of inappropriate antidiuresis,
+BMGC_DS10746,BMG_DS038863,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE",,,,,,,C1845243,,314690;300534,MONDO:0010355,syndromic X-linked intellectual disability Claes-Jensen type,
+BMGC_DS10747,BMG_DS038864,,Martin-Probst Deafness-Mental Retardation Syndrome,,,,,,,C1845285,C564495,300519,MONDO:0010353,"deafness-intellectual disability, Martin-Probst type syndrome",
+BMGC_DS10748,BMG_DS038865,,,,,,,,,C1845286,,300518,MONDO:0010352,"intellectual disability, X-linked 82",
+BMGC_DS10749,BMG_DS038866,,"FANCONI ANEMIA, COMPLEMENTATION GROUP B",,,,,DOID:0111098,Fanconi anemia complementation group B,C1845292,,300514;300515,MONDO:0010351,Fanconi anemia complementation group B,
+BMGC_DS10750,BMG_DS038867,,Premature Ovarian Failure 2a,,,,,,,C1845293,C564498,300511,MONDO:0010350,premature ovarian failure 2A,
+BMGC_DS10751,BMG_DS038868,,Ovarian Dysgenesis 2,,,,,DOID:0080494,ovarian dysgenesis 2,C1845294,C564499,300510,MONDO:0010349,ovarian dysgenesis 2,
+BMGC_DS10752,BMG_DS038869,,Premature Ovarian Failure 4,,,,,DOID:0080494,ovarian dysgenesis 2,C1845295,C564499,,MONDO:0800317,premature ovarian failure 4,
+BMGC_DS10753,BMG_DS038871,,,,,,,,,C1845297,,300505,MONDO:0010347,"intellectual disability, X-linked 84",
+BMGC_DS10754,BMG_DS038872,,,,,,,,,C1845333,,300498,MONDO:0010344,"intellectual disability, X-linked 45",
+BMGC_DS10755,BMG_DS038873,,,,,,,,,C1845336,,300496,MONDO:0010342,"autism, susceptibility to, X-linked 3",
+BMGC_DS10756,BMG_DS038874,,"Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders",,,,,DOID:0112122,X-linked epilepsy with variable learning disabilities and behavior disorders,C1845343,C564505,,,,
+BMGC_DS10757,BMG_DS038875,,"Spinal Muscular Atrophy, Distal, X-Linked 3",,,,,DOID:0111196,X-linked distal spinal muscular atrophy 3,C1845359,C564506,300489,MONDO:0010338,X-linked distal spinal muscular atrophy type 3,
+BMGC_DS10758,BMG_DS038876,,"Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance",,,,,,,C1845366,C537456,300486,MONDO:0010337,X-linked intellectual disability-cerebellar hypoplasia syndrome,
+BMGC_DS10759,BMG_DS038878,,"CONE-ROD DYSTROPHY, X-LINKED, 3",,,,,DOID:0111007,X-linked cone-rod dystrophy 3,C1845407,,300110;300476,MONDO:0010335,X-linked cone-rod dystrophy 3,
+BMGC_DS10760,BMG_DS038879,,"Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia",,,,,,,C1845446,C564509,300472,MONDO:0010333,corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome,
+BMGC_DS10761,BMG_DS038882,,,,,,,,,C1845499,,300454,MONDO:0010329,"intellectual disability, X-linked 77",
+BMGC_DS10762,BMG_DS038883,,,,,,,,,C1845526,,300436,MONDO:0010326,"intellectual disability, X-linked 46",
+BMGC_DS10763,BMG_DS038884,,Stocco dos Santos syndrome,,,,,,,C1845530,C537495,300434,MONDO:0010325,"X-linked intellectual disability, Stocco dos Santos type",
+BMGC_DS10764,BMG_DS038885,,,,,,,,,C1845531,,300433,MONDO:0010324,"intellectual disability, X-linked 81",
+BMGC_DS10765,BMG_DS038886,,,,,,,,,C1845539,,300495,MONDO:0010341,"autism, susceptibility to, X-linked 2",
+BMGC_DS10766,BMG_DS038887,,,,,,,,,C1845540,,300425,MONDO:0010321,"autism, susceptibility to, X-linked 1",
+BMGC_DS10767,BMG_DS038888,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HEDERA TYPE",,,,,DOID:0060806,syndromic X-linked intellectual disability Hedera type,C1845543,,300556;300423,MONDO:0010319,syndromic X-linked intellectual disability Hedera type,
+BMGC_DS10768,BMG_DS038889,,FG syndrome 4,,,,,,,C1845546,C537923,300422,MONDO:0010318,FG syndrome 4,
+BMGC_DS10769,BMG_DS038890,,FG SYNDROME 3,,,,,,,C1845567,,300406,MONDO:0010316,FG syndrome 3,
+BMGC_DS10770,BMG_DS038894,,RETINITIS PIGMENTOSA 3,,,,,,,C1845667,,312610;300029,MONDO:0010227,retinitis pigmentosa 3,
+BMGC_DS10771,BMG_DS038895,,Perisylvian syndrome,,,,,,,C1845668,C536658,,MONDO:0020340,bilateral perisylvian polymicrogyria,
+BMGC_DS10772,BMG_DS038896,,,,,,,,,C1845672,,300387,MONDO:0010313,"intellectual disability, X-linked 63",
+BMGC_DS10773,BMG_DS038899,,Dyserythropoietic Anemia with Thrombocytopenia,,,,,,,C1845837,C564525,,MONDO:0100089,GATA1-Related X-Linked Cytopenia,
+BMGC_DS10774,BMG_DS038902,,,,,,,,,C1845860,,300355,MONDO:0010307,"intellectual disability, X-linked 73",
+BMGC_DS10775,BMG_DS038903,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE",,,,,,,C1845861,,300304;300354,MONDO:0010306,"X-linked intellectual disability, Cabezas type",
+BMGC_DS10776,BMG_DS038904,,"Creatine deficiency, X-linked",,,,,,,C1845862,C535598,300352,MONDO:0010305,creatine transporter deficiency,
+BMGC_DS10777,BMG_DS038906,,,,,,,,,C1845889,,300324,MONDO:0010300,"intellectual disability, X-linked 53",
+BMGC_DS10778,BMG_DS038907,,"Lesch-Nyhan Syndrome, Neurologic Variant",,,,,,,C1845892,C564535,,,,
+BMGC_DS10779,BMG_DS038908,,FG SYNDROME 2,,,,,,,C1845902,,300017;300321,MONDO:0010297,FG syndrome 2,
+BMGC_DS10780,BMG_DS038909,,"Agammaglobulinemia, X-linked, type 2",,,,,DOID:0111999,immunodeficiency 61,C1845903,C538057,300310,MONDO:0010296,immunodeficiency 61,
+BMGC_DS10781,BMG_DS038911,,"Neutropenia, Severe Congenital, X-Linked",,,,,DOID:0112128,X-linked severe congenital neutropenia,C1845987,C564539,300299,MONDO:0010294,X-linked severe congenital neutropenia,
+BMGC_DS10782,BMG_DS038912,,"Ectodermal dysplasia, hypohidrotic, with immune deficiency",,,,,,,C1846006,C536181,,MONDO:0010293,ectodermal dysplasia and immune deficiency,
+BMGC_DS10783,BMG_DS038913,,,,,,,,,C1846008,,300291,MONDO:0020740,ectodermal dysplasia and immunodeficiency 1,
+BMGC_DS10784,BMG_DS038914,702384004,"Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaly syndrome",,,,,,,C1846009,,614732,MONDO:0013873,IMAGe syndrome,"Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaly syndrome | Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaly syndrome (disorder) | IMAGe syndrome"
+BMGC_DS10785,BMG_DS038915,,URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME,,,,,,,C1846010,,300163;300280,MONDO:0010292,Uruguay Faciocardiomusculoskeletal syndrome,
+BMGC_DS10786,BMG_DS038917,,"Goiter, Multinodular 2",,,,,,,C1846033,C564546,300273,MONDO:0010290,"goiter, multinodular 2",
+BMGC_DS10787,BMG_DS038919,,,,,,,,,C1846038,,300271,MONDO:0010289,"intellectual disability, X-linked 72",
+BMGC_DS10788,BMG_DS038921,,"Spastic paraplegia 16, X-linked",,,,,,,C1846046,C536643,300266,MONDO:0010287,hereditary spastic paraplegia 16,
+BMGC_DS10789,BMG_DS038922,,Siderius X-linked mental retardation syndrome,,,,,DOID:0060812,syndromic X-linked intellectual disability Siderius type,C1846055,C537333,300263,MONDO:0010286,syndromic X-linked intellectual disability Siderius type,
+BMGC_DS10790,BMG_DS038923,,Abidi X-linked mental retardation syndrome,,,,,DOID:0060818,syndromic X-linked intellectual disability Abidi type,C1846056,C535556,300262,MONDO:0010285,syndromic X-linked intellectual disability Abidi type,
+BMGC_DS10791,BMG_DS038924,,Armfield X-Linked Mental Retardation Syndrome,,,,,,,C1846057,C564551,300261,MONDO:0010284,Armfield syndrome,
+BMGC_DS10792,BMG_DS038925,702816000,Lubs X-linked mental retardation syndrome,,,,,DOID:0060799,syndromic X-linked intellectual disability Lubs type,C1846058,C537723,300260,MONDO:0010283,syndromic X-linked intellectual disability Lubs type,Methyl-CpG (cytosine phosphate guanine) binding protein-2 duplication syndrome | MECP2 duplication syndrome | Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome (disorder) | Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome | Lubs X-linked mental retardation syndrome | Lubs X-linked intellectual disability syndrome | Proximal Xq28 duplication syndrome
+BMGC_DS10793,BMG_DS038926,773404000,Roifman syndrome,,,,,,,C1846059,C535866,616651;300258,MONDO:0014722,Roifman syndrome,"Roifman syndrome (disorder) | Spondyloepiphyseal dysplasia, retinal dystrophy, immunodeficiency syndrome | Roifman syndrome"
+BMGC_DS10794,BMG_DS038927,,"Ptosis, Hereditary Congenital 2",,,,,,,C1846128,C564553,300245,MONDO:0010280,"ptosis, hereditary congenital 2",
+BMGC_DS10795,BMG_DS038928,,Terminal Osseous Dysplasia and Pigmentary Defects,,,,,DOID:0112149,terminal osseous dysplasia,C1846129,C564554,300244,MONDO:0010279,terminal osseous dysplasia-pigmentary defects syndrome,
+BMGC_DS10796,BMG_DS038929,,"Mental retardation X-linked, South African type",,,,,DOID:0060825,Christianson syndrome,C1846130,C537450,,,,
+BMGC_DS10797,BMG_DS038930,,HOYERAAL-HREIDARSSON SYNDROME,,,,,DOID:0070025,X-linked dyskeratosis congenita,C1846142,,305000,MONDO:0018045,Hoyeraal-Hreidarsson syndrome,
+BMGC_DS10798,BMG_DS038931,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 11",,,,,,,C1846145,,300238,MONDO:0010277,syndromic X-linked intellectual disability Shashi type,
+BMGC_DS10799,BMG_DS038933,,"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH HYPOMYELINATING LEUKODYSTROPHY",,,,,,,C1846148,,300232;300169,MONDO:0010275,"spondyloepimetaphyseal dysplasia, Bieganski type",
+BMGC_DS10800,BMG_DS038934,,,,,,,,,C1846164,,300228,MONDO:0010274,testicular germ cell tumor 1,
+BMGC_DS10801,BMG_DS038936,,Myotubular Myopathy with Abnormal Genital Development,,,,,,,C1846169,C564561,300219,MONDO:0010271,X-linked myotubular myopathy-abnormal genitalia syndrome,
+BMGC_DS10802,BMG_DS038937,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 7",,,,,DOID:0060808,syndromic X-linked intellectual disability 7,C1846170,,300218,MONDO:0010270,syndromic X-linked intellectual disability 7,
+BMGC_DS10803,BMG_DS038938,,"Lissencephaly, X-Linked, 2",,,,,,,C1846171,C564563,300215,MONDO:0010268,X-linked lissencephaly with abnormal genitalia,
+BMGC_DS10804,BMG_DS038939,,Hydranencephaly and Abnormal Genitalia,,,,,,,C1846172,C564563,,,,
+BMGC_DS10805,BMG_DS038940,,"EPISODIC MUSCLE WEAKNESS, X-LINKED",,,,,,,C1846173,,300211,MONDO:0010267,"episodic muscle weakness, X-linked",
+BMGC_DS10806,BMG_DS038941,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 58",,,,,DOID:0112024,non-syndromic X-linked intellectual disability 58,C1846174,,300210;300096,MONDO:0010266,"intellectual disability, X-linked 58",
+BMGC_DS10807,BMG_DS038942,723625009,Simpson Golabi Behmel syndrome type 2,,,,,,,C1846175,,300209,MONDO:0010265,Simpson-Golabi-Behmel syndrome type 2,Simpson Golabi Behmel syndrome type 2 (disorder) | Simpson Golabi Behmel syndrome type 2 | Lethal variant of Simpson Golabi Behmel syndrome
+BMGC_DS10808,BMG_DS038944,,"Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis",,,,,DOID:0111860,AMME complex,C1846242,C564570,300194,MONDO:0010263,Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome,
+BMGC_DS10809,BMG_DS038947,,"Microphthalmia, syndromic 2",,,,,DOID:0111809,syndromic microphthalmia 2,C1846265,C537465,300166,MONDO:0010261,"microphthalmia, syndromic 2",
+BMGC_DS10810,BMG_DS038948,,"ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED",,,,,,,C1846273,,300158,MONDO:0010260,"arthrogryposis, congenital, lower limb, X-linked",
+BMGC_DS10811,BMG_DS038949,722037004,MEHMO syndrome,,,,,DOID:0060801,MEHMO syndrome,C1846278,C537451,300987;300148,MONDO:0010258,MEHMO syndrome,"Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome | MEHMO (mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity) syndrome | MEHMO syndrome | Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome (disorder) | Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome | X-linked intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome"
+BMGC_DS10812,BMG_DS038950,,,,,,,,,C1846279,,300147,MONDO:0010257,"prostate cancer, hereditary, X-linked 1",
+BMGC_DS10813,BMG_DS038952,,Juvenile-onset dystonia,,,,,,,C1846331,C537704,,,,
+BMGC_DS10814,BMG_DS038953,,"Bartter syndrome, type 3",,,,,,,C1846343,C537653,607364,MONDO:0011822,Bartter disease type 3,
+BMGC_DS10815,BMG_DS038954,,"Bartter Syndrome, Type 3, with Hypocalciuria",,,,,,,C1846344,C564578,,,,
+BMGC_DS10816,BMG_DS038955,,Meckel syndrome type 3,,,,,,,C1846357,C536132,607361,MONDO:0011821,"Meckel syndrome, type 3",
+BMGC_DS10817,BMG_DS038957,,Spinocerebellar ataxia 19,,,,,,,C1846367,C537198,607346,MONDO:0011819,spinocerebellar ataxia type 19/22,
+BMGC_DS10818,BMG_DS038958,,,,,,,,,C1846385,,607341,MONDO:0011818,isolated focal cortical dysplasia type II,
+BMGC_DS10819,BMG_DS038959,,"Focal Cortical Dysplasia of Taylor, Type IIa",,,,,,,C1846386,C537067,,MONDO:0017101,isolated focal cortical dysplasia type IIa,
+BMGC_DS10820,BMG_DS038960,,"CORTICAL DYSPLASIA OF TAYLOR, DYSPLASIA ONLY",,,,,,,C1846388,,607341,,,
+BMGC_DS10821,BMG_DS038961,,"Focal Cortical Dysplasia of Taylor, Type IIb",,,,,,,C1846389,C537067,,,,
+BMGC_DS10822,BMG_DS038962,,"CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 1",,,,,,,C1846418,,607339,MONDO:0011817,"coronary heart disease, susceptibility to, 1",
+BMGC_DS10823,BMG_DS038963,719257008,Lathosterolosis,,,,,,,C1846421,C537880,607330,MONDO:0011816,lathosterolosis,Lathosterolosis (disorder) | Lathosterolosis | Sterol C5 desaturase deficiency
+BMGC_DS10824,BMG_DS038965,,,,,,,DOID:0060247,Smith-McCort dysplasia,C1846431,,,MONDO:0015799,Smith-McCort dysplasia,
+BMGC_DS10825,BMG_DS038966,,,,,,,,,C1846439,,613628,MONDO:0013333,odontoid hypoplasia,
+BMGC_DS10826,BMG_DS038968,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4",,,,,DOID:0111611,autosomal recessive spinocerebellar ataxia 4,C1846492,,607317;608877,MONDO:0011811,autosomal recessive cerebellar ataxia-saccadic intrusion syndrome,
+BMGC_DS10827,BMG_DS038969,702381007,Horizontal gaze palsy with progressive scoliosis,,,,,,,C1846496,,,,,Horizontal gaze palsy with progressive scoliosis | Horizontal gaze palsy with progressive scoliosis (disorder) | HGPPS - horizontal gaze palsy with progressive scoliosis | Familial infantile scoliosis associated with bilateral paralysis of conjugate gaze
+BMGC_DS10828,BMG_DS038970,,,,,,,,,C1846520,,607304,MONDO:0011808,cataract 27,
+BMGC_DS10829,BMG_DS038971,,CONE-ROD DYSTROPHY 10,,,,,,,C1846529,,607292;610283,MONDO:0012464,cone-rod dystrophy 10,
+BMGC_DS10830,BMG_DS038973,,"ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1",,,,,,,C1846534,,607277,MONDO:0011805,"asthma-related traits, susceptibility to, 1",
+BMGC_DS10831,BMG_DS038974,,Autoimmune Lymphoproliferative Syndrome Type 2B,Autoimmune Lymphoproliferative Syndrome,,,,,,C1846545,D056735,607271,MONDO:0017979;MONDO:0011804,autoimmune lymphoproliferative syndrome | autoimmune lymphoproliferative syndrome type 2B,
+BMGC_DS10832,BMG_DS038975,,"SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE",,,,,,,C1846564,,607259;602783,MONDO:0011803,hereditary spastic paraplegia 7,
+BMGC_DS10833,BMG_DS038978,,"DEAFNESS, AUTOSOMAL RECESSIVE 33",,,,,,,C1846576,,607239,MONDO:0011799,autosomal recessive nonsyndromic hearing loss 33,
+BMGC_DS10834,BMG_DS038979,,"Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration",,,,,,,C1846582,C564603,607236,MONDO:0011798,"hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration",
+BMGC_DS10835,BMG_DS038983,,Thyroid Dyshormonogenesis 6,,,,,DOID:0112189,thyroid dyshormonogenesis 6,C1846632,C564608,607200,MONDO:0011792,thyroid dyshormonogenesis 6,
+BMGC_DS10836,BMG_DS038984,,"Deafness, Autosomal Recessive",,,,,,,C1846647,C564609,607197,MONDO:0019588,"hearing loss, autosomal recessive",
+BMGC_DS10837,BMG_DS038985,702437000,Amish lethal microcephaly,,,,,,,C1846648,C538247,607196,MONDO:0011790,Amish lethal microcephaly,Amish lethal microcephaly (disorder) | Amish microcephaly | Amish lethal microcephaly
+BMGC_DS10838,BMG_DS038987,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I",,,,,,,C1846672,,607155,MONDO:0011787,autosomal recessive limb-girdle muscular dystrophy type 2I,
+BMGC_DS10839,BMG_DS038988,,"Spastic paraplegia 19, autosomal dominant",,,,,,,C1846685,C536856,607152,MONDO:0011785,hereditary spastic paraplegia 19,
+BMGC_DS10840,BMG_DS038989,,MOYAMOYA DISEASE 2,,,,,,,C1846689,,607151,MONDO:0011784,Moyamoya disease 2,
+BMGC_DS10841,BMG_DS038990,,SPINOCEREBELLAR ATAXIA 17,,,,,DOID:0050967,spinocerebellar ataxia type 17,C1846707,,607136;164700;213100;607136;600075,MONDO:0011781,spinocerebellar ataxia type 17,
+BMGC_DS10842,BMG_DS038991,,SPECIFIC LANGUAGE IMPAIRMENT 3,,,,,,,C1846719,,607134,MONDO:0011780,specific language impairment 3,
+BMGC_DS10843,BMG_DS038993,,Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies,,,,,,,C1846722,C564621,607131,MONDO:0011778,"multiple epiphyseal dysplasia, Al-Gazali type",
+BMGC_DS10844,BMG_DS038995,,,,,,,,,C1846758,,607107,MONDO:0011775,"nasopharyngeal carcinoma, susceptibility to, 1",
+BMGC_DS10845,BMG_DS038996,,"Deafness, Autosomal Recessive 30",,,,,,,C1846784,C564624,607101,MONDO:0011774,autosomal recessive nonsyndromic hearing loss 30,
+BMGC_DS10846,BMG_DS038997,,Joubert syndrome 4,,,,,DOID:0110999,Joubert syndrome 4,C1846790,C536296,609583,MONDO:0012308,Joubert syndrome with renal defect,
+BMGC_DS10847,BMG_DS038998,764460003,Anauxetic dysplasia,,,,,DOID:0080942,anauxetic dysplasia,C1846796,C538256,,MONDO:0011773,anauxetic dysplasia,Anauxetic dysplasia | Spondyloepimetaphyseal dysplasia anauxetic type (disorder) | Spondyloepimetaphyseal dysplasia Menger type | Spondyloepimetaphyseal dysplasia anauxetic type
+BMGC_DS10848,BMG_DS039000,,"Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3",,,,,DOID:0111211,autosomal recessive distal hereditary motor neuronopathy 3,C1846823,C564626,607088,MONDO:0011771,"neuronopathy, distal hereditary motor, autosomal recessive 3",
+BMGC_DS10849,BMG_DS039001,,"Aortic Aneurysm, Familial Thoracic 2",,,,,,,C1846837,C564627,607087,MONDO:0011770,"aortic aneurysm, familial thoracic 2",
+BMGC_DS10850,BMG_DS039003,,"DEAFNESS, AUTOSOMAL RECESSIVE 31",,,,,,,C1846839,,607084;607928,MONDO:0011767,autosomal recessive nonsyndromic hearing loss 31,
+BMGC_DS10851,BMG_DS039004,,"EPIPHYSEAL DYSPLASIA, MULTIPLE, 5",,,,,DOID:0070299,multiple epiphyseal dysplasia 5,C1846843,,602109;607078,MONDO:0011765,multiple epiphyseal dysplasia type 5,
+BMGC_DS10852,BMG_DS039006,,"PARKINSON DISEASE 8, AUTOSOMAL DOMINANT",,,,,DOID:0060371,Parkinson's disease 8,C1846862,,609007;607060,MONDO:0011764,autosomal dominant Parkinson disease 8,
+BMGC_DS10853,BMG_DS039007,,"Deafness, Autosomal Recessive 22",,,,,,,C1846896,C564633,607039,MONDO:0011762,autosomal recessive nonsyndromic hearing loss 22,
+BMGC_DS10854,BMG_DS039008,,"Deafness, Autosomal Dominant 21",,,,,,,C1846922,C564634,607017,MONDO:0011761,autosomal dominant nonsyndromic hearing loss 21,
+BMGC_DS10855,BMG_DS039009,,"Brachydactyly, Type A1, B",,,,,,,C1846949,C564635,607004,MONDO:0011757,brachydactyly type A1B,
+BMGC_DS10856,BMG_DS039010,,SENIOR-LOKEN SYNDROME 4,,,,,,,C1846979,,607215;606996,MONDO:0011756,Senior-Loken syndrome 4,
+BMGC_DS10857,BMG_DS039011,,Senior-Loken Syndrome 3,,,,,,,C1846980,C564637,606995,MONDO:0011755,senior-loken syndrome 3,
+BMGC_DS10858,BMG_DS039012,,"Hyperreninemic Hypoaldosteronism, Familial, 2",,,,,,,C1846990,C564638,606984,MONDO:0011754,familial hyperreninemic hypoaldosteronism type 2,
+BMGC_DS10859,BMG_DS039014,,NEPHRONOPHTHISIS 4,,,,,,,C1847013,,606966;607215,MONDO:0011752,nephronophthisis 4,
+BMGC_DS10860,BMG_DS039015,,"PULMONARY DISEASE, CHRONIC OBSTRUCTIVE, SEVERE EARLY-ONSET",,,,,,,C1847014,,606963,MONDO:0011751,"COPD, severe early onset",
+BMGC_DS10861,BMG_DS039016,,Oculocutaneous albinism type 1B,,,,,DOID:0070095,oculocutaneous albinism type IB,C1847024,C537729,606952,MONDO:0011749,oculocutaneous albinism type 1B,
+BMGC_DS10862,BMG_DS039017,,"USHER SYNDROME, TYPE IG",,,,,,,C1847089,,607696;606943,MONDO:0011748,Usher syndrome type 1G,
+BMGC_DS10863,BMG_DS039018,,"ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE",,,,,,,C1847132,,606952,MONDO:0018137,temperature-sensitive oculocutaneous albinism type 1,
+BMGC_DS10864,BMG_DS039020,,"Symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch",,,,,,,C1847185,C538148,606895,MONDO:0011746,"symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch",
+BMGC_DS10865,BMG_DS039022,,"Vascular Malformation, Primary Intraosseous",,,,,,,C1847197,C564648,606893,MONDO:0011744,primary intraosseous venous malformation,
+BMGC_DS10866,BMG_DS039023,,ALZHEIMER DISEASE 4,,,,,DOID:0110040,Alzheimer's disease 4,C1847200,,606889,MONDO:0011743,Alzheimer disease 4,
+BMGC_DS10867,BMG_DS039024,722377004,Paraganglioma and gastric stromal sarcoma syndrome,,,,,,,C1847319,,606864,MONDO:0011740,Carney-Stratakis syndrome,Paraganglioma and gastric stromal sarcoma syndrome (disorder) | Carney Stratakis syndrome | Paraganglioma and gastric stromal sarcoma syndrome | Carney Stratakis dyad
+BMGC_DS10868,BMG_DS039025,,,,,,,,,C1847351,,606856,MONDO:0011739,"pancreatic cancer, susceptibility to, 1",
+BMGC_DS10869,BMG_DS039026,,"POLYMICROGYRIA, BILATERAL FRONTOPARIETAL",,,,,DOID:0080922,bilateral frontoparietal polymicrogyria,C1847352,,606854,MONDO:0011738,bilateral frontoparietal polymicrogyria,
+BMGC_DS10870,BMG_DS039028,,Cree Mental Retardation Syndrome,,,,,,,C1847361,C564654,606851,MONDO:0011736,Cree intellectual disability syndrome,
+BMGC_DS10871,BMG_DS039029,,Cardioneuromyopathy with Hyaline Masses and Nemaline Rods,,,,,,,C1847387,C564655,606842,MONDO:0011734,Cardioneuromyopathy with hyaline masses and nemaline rods,
+BMGC_DS10872,BMG_DS039030,,"Faciomandibular myoclonus, nocturnal",,,,,,,C1847399,C536389,606840,MONDO:0011733,"parasomnia, sleep bruxism type",
+BMGC_DS10873,BMG_DS039031,,"Digital Arthropathy-Brachydactyly, Familial",,,,,,,C1847406,C564656,606835,MONDO:0011732,familial digital arthropathy-brachydactyly,
+BMGC_DS10874,BMG_DS039032,,FRIEDREICH ATAXIA WITH RETAINED REFLEXES,,,,,,,C1847416,,229300;606829,MONDO:0800301,Friedreich ataxia with retained reflexes,
+BMGC_DS10875,BMG_DS039034,,,,,,,,,C1847492,,606788,MONDO:0011727,"anorexia nervosa, susceptibility to, 1",
+BMGC_DS10876,BMG_DS039035,,Peripheral Arterial Occlusive Disease 1,,,,,,,C1847493,C564658,606787,MONDO:0011726,peripheral arterial occlusive disease 1,
+BMGC_DS10877,BMG_DS039036,,Glut1 Deficiency Syndrome,,,,,DOID:0070560,glucose transporter type 1 deficiency syndrome,C1847501,C536830,,MONDO:0000188,GLUT1 deficiency syndrome,
+BMGC_DS10878,BMG_DS039037,,,,,,,,,C1847521,,606773,MONDO:0011723,hemifacial myohyperplasia,
+BMGC_DS10879,BMG_DS039038,,MOMES Syndrome,,,,,,,C1847522,C564660,606772,MONDO:0011722,intellectual disability-obesity-prognathism-eye and skin anomalies syndrome,
+BMGC_DS10880,BMG_DS039039,,Hyperopic Astigmatism,Astigmatism,,,,,,C1847524,D001251,,,,
+BMGC_DS10881,BMG_DS039040,,"MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET",,,,,DOID:0111187,distal myopathy with anterior tibial onset,C1847532,,603009;606768,MONDO:0011721,distal myopathy with anterior tibial onset,
+BMGC_DS10882,BMG_DS039041,,"Azoospermia, Nonobstructive",,,,,,,C1847540,C564665,,,,
+BMGC_DS10883,BMG_DS039042,,"Primary ciliary dyskinesia, 2",,,,,,,C1847554,C535277,606763,MONDO:0011718,primary ciliary dyskinesia 2,
+BMGC_DS10884,BMG_DS039043,,"Hyperinsulinemic hypoglycemia, familial, 6",,,,,,,C1847555,C538375,606762,MONDO:0011717,hyperinsulinism-hyperammonemia syndrome,
+BMGC_DS10885,BMG_DS039044,,SECKEL SYNDROME 2,,,,,,,C1847572,,604124;606744,MONDO:0011715,Seckel syndrome 2,
+BMGC_DS10886,BMG_DS039046,,"EPIPHYSEAL DYSPLASIA, MULTIPLE, 4",,,,,DOID:0070300,multiple epiphyseal dysplasia 4,C1847593,,606718;226900,MONDO:0009189,multiple epiphyseal dysplasia type 4,
+BMGC_DS10887,BMG_DS039047,,Van der Woude syndrome 2,,,,,,,C1847604,C536529,606713,MONDO:0011712,van der Woude syndrome 2,
+BMGC_DS10888,BMG_DS039048,,SPECIFIC LANGUAGE IMPAIRMENT 2,,,,,,,C1847605,,606712,MONDO:0011711,specific language impairment 2,
+BMGC_DS10889,BMG_DS039049,,SPECIFIC LANGUAGE IMPAIRMENT 1,,,,,,,C1847614,,606711,MONDO:0011710,specific language impairment 1,
+BMGC_DS10890,BMG_DS039051,,"Deafness, Autosomal Dominant 36",,,,,,,C1847626,C564675,606705,MONDO:0011708,autosomal dominant nonsyndromic hearing loss 36,
+BMGC_DS10891,BMG_DS039052,,"Dyskinesia, Familial, with Facial Myokymia",,,,,,,C1847627,C564676,,,,
+BMGC_DS10892,BMG_DS039053,,KUFOR-RAKEB SYNDROME,,,,,DOID:0060556,Kufor-Rakeb syndrome,C1847640,,606693;610513,MONDO:0011706,Kufor-Rakeb syndrome,
+BMGC_DS10893,BMG_DS039055,,SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES,,,,,,,C1847650,,606688;176640,MONDO:0011703,spongiform encephalopathy with neuropsychiatric features,
+BMGC_DS10894,BMG_DS039056,,"CARDIOMYOPATHY, DILATED, 1L",,,,,,,C1847667,,606685;601411,MONDO:0011702,dilated cardiomyopathy 1L,
+BMGC_DS10895,BMG_DS039059,,,,,,,,,C1847711,,258660,MONDO:0009789,"nonarteritic anterior ischemic optic neuropathy, susceptibility to",
+BMGC_DS10896,BMG_DS039061,763720007,Hypermethioninemia due to deficiency of glycine N-methyltransferase,,,,,,,C1847720,,606664,MONDO:0011698,glycine N-methyltransferase deficiency,Hypermethioninemia due to deficiency of glycine N-methyltransferase | Hypermethioninaemia due to GNMT (glycine N-methyltransferase) deficiency | Hypermethioninemia due to GNMT (glycine N-methyltransferase) deficiency | Hypermethioninemia due to deficiency of glycine N-methyltransferase (disorder) | Hypermethioninaemia due to deficiency of glycine N-methyltransferase | Glycine N-methyltransferase deficiency
+BMGC_DS10897,BMG_DS039063,,,,,,,,,C1847723,,606661,MONDO:0011696,"melanoma, uveal, susceptibility to, 2",
+BMGC_DS10898,BMG_DS039064,,,,,,,,,C1847724,,606660,MONDO:0011695,"melanoma, uveal, susceptibility to, 1",
+BMGC_DS10899,BMG_DS039065,,SPINOCEREBELLAR ATAXIA 15,,,,,DOID:0050965,spinocerebellar ataxia type 15,C1847725,,606658;147265,MONDO:0011694,spinocerebellar ataxia type 15/16,
+BMGC_DS10900,BMG_DS039066,,,,,,,,,C1847730,,606657,MONDO:0011693,"glaucoma, normal tension, susceptibility to",
+BMGC_DS10901,BMG_DS039068,,Amyotrophic Lateral Sclerosis 3,,,,,,,C1847735,C564688,606640,MONDO:0011691,amyotrophic lateral sclerosis type 3,
+BMGC_DS10902,BMG_DS039070,,"MUSCULAR DYSTROPHY, CONGENITAL, 1C",,,,,,,C1847759,,606612,MONDO:0011688,muscular dystrophy-dystroglycanopathy type B5,
+BMGC_DS10903,BMG_DS039071,,Waardenburg Syndrome Type 1,Waardenburg Syndrome,,,,DOID:0110948;DOID:9258,Waardenburg syndrome type 1 | Waardenburg syndrome,C1847800,D014849,193500,MONDO:0008670,Waardenburg syndrome type 1,
+BMGC_DS10904,BMG_DS039072,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F",,,,,,,C1847823,,606595;602195,MONDO:0011687,Charcot-Marie-Tooth disease axonal type 2F,
+BMGC_DS10905,BMG_DS039073,,LIG4 Syndrome,,,,,,,C1847827,C564694,606593,MONDO:0011686,DNA ligase IV deficiency,
+BMGC_DS10906,BMG_DS039074,,,,,,,,,C1847831,,606581,MONDO:0011685,"polysubstance abuse, susceptibility to",
+BMGC_DS10907,BMG_DS039075,,,,,,,,,C1847835,,606579,MONDO:0011684,vitiligo-associated multiple autoimmune disease susceptibility 1,
+BMGC_DS10908,BMG_DS039076,,"Oculocutaneous Albinism, Type IV",,,,,,,C1847836,C564696,606574,MONDO:0011683,oculocutaneous albinism type 4,
+BMGC_DS10909,BMG_DS039077,,"Episodic Ataxia, Type 3",,,,,,,C1847839,C564697,606554,MONDO:0011682,episodic ataxia type 3,
+BMGC_DS10910,BMG_DS039078,,"EPISODIC ATAXIA, TYPE 4",,,,,DOID:0050992,episodic ataxia type 4,C1847843,,606552,MONDO:0011681,episodic ataxia type 4,
+BMGC_DS10911,BMG_DS039080,,Homozygous 11p15-p14 Deletion Syndrome,,,,,,,C1847866,C564701,606528,MONDO:0011678,homozygous 11P15-p14 deletion syndrome,
+BMGC_DS10912,BMG_DS039082,,PHACE association,,,,,,,C1847874,C537892,606519,MONDO:0011676,PHACE syndrome,
+BMGC_DS10913,BMG_DS039083,,"Charcot-Marie-Tooth Disease, Dominant Intermediate A",,,,,DOID:0110202,Charcot-Marie-Tooth disease dominant intermediate A,C1847896,C564702,620378,MONDO:0957273,"Charcot-Marie-Tooth disease, dominant intermediate A",
+BMGC_DS10914,BMG_DS039084,,"Charcot-Marie-Tooth Disease, Dominant Intermediate B",,,,,DOID:0110197,Charcot-Marie-Tooth disease dominant intermediate B,C1847902,C564703,606482,MONDO:0011674,Charcot-Marie-Tooth disease dominant intermediate B,
+BMGC_DS10915,BMG_DS039085,,"Charcot-Marie-Tooth Neuropathy, Dominant Intermediate B, with Neutropenia",,,,,,,C1847903,C564704,,,,
+BMGC_DS10916,BMG_DS039086,1156768008,Ovarioleukodystrophy,,,,,,,C1847967,C565836,,,,Ovarioleukodystrophy | Ovarioleukodystrophy (disorder) | Ovarioleucodystrophy
+BMGC_DS10917,BMG_DS039087,,"Deafness, Autosomal Dominant 30",,,,,,,C1847972,C564706,606451,MONDO:0011673,autosomal dominant nonsyndromic hearing loss 30,
+BMGC_DS10918,BMG_DS039088,,Persistent Polyclonal B-Cell Lymphocytosis,,,,,,,C1847973,C564707,606445,MONDO:0011672,persistent polyclonal B-cell lymphocytosis,
+BMGC_DS10919,BMG_DS039089,,HUNTINGTON DISEASE-LIKE 2,,,,,,,C1847987,,605268;606438,MONDO:0011671,Huntington disease-like 2,
+BMGC_DS10920,BMG_DS039090,,Ehlers-Danlos syndrome caused by tenascin-X deficiency,,,,,,,C1848029,C536193,606408,MONDO:0011670,Ehlers-Danlos syndrome due to tenascin-X deficiency,
+BMGC_DS10921,BMG_DS039091,,Hypotonia-Cystinuria Syndrome,,,,,DOID:0060858,hypotonia-cystinuria syndrome,C1848030,C564710,606407,MONDO:0011669,hypotonia-cystinuria syndrome,
+BMGC_DS10922,BMG_DS039093,,,,,,,,,C1848066,,300125,MONDO:0010253,"migraine, familial typical, susceptibility to, 2",
+BMGC_DS10923,BMG_DS039094,,"Mental Retardation, X-Linked, with Isolated Growth Hormone Deficiency",,,,,,,C1848068,C564712,,MONDO:0019032,X-linked intellectual disability with isolated growth hormone deficiency,
+BMGC_DS10924,BMG_DS039095,,Lissencephaly and agenesis of corpus callosum,,,,,,,C1848070,C531731,,,,
+BMGC_DS10925,BMG_DS039096,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 50",,,,,DOID:0112029,non-syndromic X-linked intellectual disability 50,C1848087,,300115;313440,MONDO:0010251,"intellectual disability, X-linked 50",
+BMGC_DS10926,BMG_DS039097,,"Spondyloepimetaphyseal Dysplasia, X-Linked",,,,,DOID:0112150,X-linked spondyloepimetaphyseal dysplasia,C1848097,C564714,300106,MONDO:0010248,X-linked spondyloepimetaphyseal dysplasia,
+BMGC_DS10927,BMG_DS039098,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 9,,,,,DOID:0060848,developmental and epileptic encephalopathy 9,C1848137,,300460;300088,MONDO:0010246,"developmental and epileptic encephalopathy, 9",
+BMGC_DS10928,BMG_DS039099,,"X Inactivation, Familial Skewed, 1",,,,,,,C1848138,C564716,300087,MONDO:0026404,"X inactivation, familial skewed, 1",
+BMGC_DS10929,BMG_DS039100,,"CONE-ROD DYSTROPHY, X-LINKED, 2",,,,,DOID:0111006,X-linked cone-rod dystrophy 2,C1848139,,300085,MONDO:0010245,X-linked cone-rod dystrophy 2,
+BMGC_DS10930,BMG_DS039101,,"COGNITIVE FUNCTION 1, SOCIAL",,,,,,,C1848140,,300082,MONDO:0010244,CGF1,
+BMGC_DS10931,BMG_DS039102,719827008,Woods Black Norbury syndrome,,,,,,,C1848144,C536743,300076,MONDO:0010243,X-linked immunoneurologic disorder,X-linked immunoneurologic disorder (disorder) | X-linked immunoneurologic disorder | Woods Black Norbury syndrome
+BMGC_DS10932,BMG_DS039103,,"Fetal akinesia syndrome, X-linked",,,,,,,C1848171,C537921,300073,MONDO:0010242,"fetal akinesia syndrome, X-linked",
+BMGC_DS10933,BMG_DS039104,,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A",,,,,DOID:0110871,congenital stationary night blindness 2A,C1848172,,300110;300071,MONDO:0010241,congenital stationary night blindness 2A,
+BMGC_DS10934,BMG_DS039106,,X-Linked Lissencephaly,Classical Lissencephalies and Subcortical Band Heterotopias,,,,DOID:0060402,chromosome 17p13.1 deletion syndrome,C1848199,D054221,,,,
+BMGC_DS10935,BMG_DS039107,,"SUBCORTICAL BAND HETEROTOPIA, X-LINKED",,,,,DOID:0112239,X-linked lissencephaly 1,C1848200,,300067,,,
+BMGC_DS10936,BMG_DS039108,,Subcortical Band Heterotopia,Classical Lissencephalies and Subcortical Band Heterotopias,,,,DOID:0060402;DOID:0111169,subcortical band heterotopia | chromosome 17p13.1 deletion syndrome,C1848201,D054221,,MONDO:0020491,subcortical band heterotopia,
+BMGC_DS10937,BMG_DS039109,,"Deafness, X-Linked 4",,,,,,,C1848204,C564723,300066,MONDO:0010238,"hearing loss, X-linked 4",
+BMGC_DS10938,BMG_DS039111,,"Periventricular Heterotopia, X-Linked",Periventricular Nodular Heterotopia,,,,DOID:0050454,periventricular nodular heterotopia,C1848213,D054091,300049,MONDO:0010233,"heterotopia, periventricular, X-linked dominant",
+BMGC_DS10939,BMG_DS039113,,DOSAGE-SENSITIVE SEX REVERSAL,,,,,DOID:0111777,"46,XY sex reversal 2",C1848296,,300018,MONDO:0010226,"46,XY sex reversal 2",
+BMGC_DS10940,BMG_DS039114,,Dent disease 1,,,,,DOID:0081453,Dent disease 1,C1848336,C538212,300009,MONDO:0010225,Dent disease type 1,
+BMGC_DS10941,BMG_DS039116,,Zunich neuroectodermal syndrome,,,,,DOID:0112152,CHIME syndrome,C1848392,C536729,280000,MONDO:0010221,CHIME syndrome,
+BMGC_DS10942,BMG_DS039118,,"Xeroderma pigmentosum, variant type",,,,,DOID:0110847,xeroderma pigmentosum variant type,C1848410,C536766,278750,MONDO:0010214,xeroderma pigmentosum variant type,
+BMGC_DS10943,BMG_DS039119,,"XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E",,,,,,,C1848411,,278740,MONDO:0010213,xeroderma pigmentosum group E,
+BMGC_DS10944,BMG_DS039122,,"WOOLLY HAIR, AUTOSOMAL RECESSIVE 1, WITH OR WITHOUT HYPOTRICHOSIS",,,,,DOID:0110705,hypotrichosis 8,C1848435,,278150;609239,MONDO:0800312,"wooly hair, autosomal recessive 1, with or without hypotrichosis",
+BMGC_DS10945,BMG_DS039123,,Mental retardation Wolff type,,,,,,,C1848439,C537448,277990,MONDO:0010203,"intellectual disability, Wolff type",
+BMGC_DS10946,BMG_DS039125,,WHITE FORELOCK WITH MALFORMATIONS,,,,,,,C1848463,,277740,MONDO:0010199,white forelock with malformations,
+BMGC_DS10947,BMG_DS039126,,"Whistling face syndrome, recessive form",,,,,,,C1848470,C536699,277720,MONDO:0010197,"whistling face syndrome, recessive form",
+BMGC_DS10948,BMG_DS039128,699313003,Pierre Robin syndrome with fetal chondrodysplasia,,,,,,,C1848488,C535776,184840;277610,MONDO:0008490,"otospondylomegaepiphyseal dysplasia, autosomal dominant",Weissenbacher-Zweymuller syndrome | Heterozygous OSMED (otospondylomegaepiphyseal dysplasia) | Heterozygous otospondylomegaepiphyseal dysplasia | Weissenbacher-Zweymuller syndrome (disorder) | Pierre Robin syndrome with fetal chondrodysplasia
+BMGC_DS10949,BMG_DS039129,,"WAARDENBURG SYNDROME, TYPE 4A",,,,,DOID:0110953,Waardenburg syndrome type 4A,C1848519,,131244;277580,MONDO:0010192,Waardenburg syndrome type 4A,
+BMGC_DS10950,BMG_DS039131,,Pontocerebellar Hypoplasia Type 2A,,,,,DOID:0060267,pontocerebellar hypoplasia type 2A,C1848526,C564738,277470,MONDO:0010190,pontocerebellar hypoplasia type 2A,
+BMGC_DS10951,BMG_DS039134,702442008,Ataxia with vitamin E deficiency,,,,,DOID:0090028,familial isolated deficiency of vitamin E,C1848533,C535393,277460,MONDO:0010188,familial isolated deficiency of vitamin E,Familial isolated vitamin E deficiency | Friedreich-like ataxia | Ataxia with vitamin E deficiency (disorder) | Ataxia with vitamin E deficiency | Ataxia with isolated vitamin E deficiency | Friedreich ataxia phenotype with selective vitamin E deficiency
+BMGC_DS10952,BMG_DS039135,,"VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1",,,,,DOID:0112173,combined deficiency of vitamin K-dependent clotting factors 1,C1848534,,137167;277450,MONDO:0010187,"vitamin K-dependent clotting factors, combined deficiency of, type 1",
+BMGC_DS10953,BMG_DS039136,,"Methylmalonic Aciduria and Homocystinuria, CblD Type",,,,,,,C1848552,C564743,277410,MONDO:0010185,methylmalonic aciduria and homocystinuria type cblD,
+BMGC_DS10954,BMG_DS039137,,"Homocystinuria, CblD Type, Variant 1",,,,,,,C1848553,C564743,,,,
+BMGC_DS10955,BMG_DS039138,,"Methylmalonic Aciduria, CblD Type, Variant 2",,,,,,,C1848554,C564743,,MONDO:0017685,"vitamin B12-responsive methylmalonic acidemia, type cblDv2",
+BMGC_DS10956,BMG_DS039139,74653006,Cobalamin C disease,,,,,,,C1848561,,277400,MONDO:0010184,methylmalonic aciduria and homocystinuria type cblC,Cobalamin C disease | Cobalamin C disease (disorder) | CblC methylmalonic acidaemia and homocystinuria | CblC methylmalonic acidemia and homocystinuria | Cobalamin locus C variant | CblC - Cobalamin locus C
+BMGC_DS10957,BMG_DS039140,,"Methylmalonic Aciduria and Homocystinuria, CblF Type",,,,,,,C1848578,C564747,277380,MONDO:0010183,methylmalonic aciduria and homocystinuria type cblF,
+BMGC_DS10958,BMG_DS039141,,Visceral myopathy familial external ophthalmoplegia,,,,,DOID:0080127;DOID:0070331;DOID:0080119,mitochondrial DNA depletion syndrome 8b | mitochondrial DNA depletion syndrome 8a | mitochondrial DNA depletion syndrome 1,C1848586,C536350,277320,MONDO:0010181,oculogastrointestinal muscular dystrophy,
+BMGC_DS10959,BMG_DS039142,,Isolated hypoplasia of the right ventricle,,,,,,,C1848587,C535682,277200,MONDO:0010179,isolated right ventricular hypoplasia,
+BMGC_DS10960,BMG_DS039143,,Vascular Hyalinosis,,,,,,,C1848590,C564750,277175,MONDO:0010177,vascular hyalinosis,
+BMGC_DS10961,BMG_DS039144,,Van Bogaert-Hozay syndrome,,,,,,,C1848598,C536526,277150,MONDO:0010175,van Bogaert-Hozay syndrome,
+BMGC_DS10962,BMG_DS039145,,VACTERL Association With Hydrocephalus,,,,,,,C1848599,C564751,276950,MONDO:0010172,VACTERL with hydrocephalus,
+BMGC_DS10963,BMG_DS039147,,"USHER SYNDROME, TYPE IC",,,,,,,C1848604,,276904;605242,MONDO:0010171,Usher syndrome type 1C,
+BMGC_DS10964,BMG_DS039148,,"USHER SYNDROME, TYPE IIA",,,,,,,C1848634,,276901;608400,MONDO:0010169,Usher syndrome type 2A,
+BMGC_DS10965,BMG_DS039151,,Ulnar Agenesis and Endocardial Fibroelastosis,,,,,,,C1848649,C564756,276822,MONDO:0010166,ulnar agenesis and endocardial fibroelastosis,
+BMGC_DS10966,BMG_DS039152,,Ulnar Hypoplasia with Mental Retardation,,,,,,,C1848650,C564757,276821,MONDO:0010165,ulna hypoplasia-intellectual disability syndrome,
+BMGC_DS10967,BMG_DS039153,,Al Awadi syndrome,,,,,,,C1848651,C535612,276820,MONDO:0010164,"phocomelia, Schinzel type",
+BMGC_DS10968,BMG_DS039156,,,,,,,,,C1848724,,276200,MONDO:0010158,T-substance anomaly,
+BMGC_DS10969,BMG_DS039157,,Distal amyotrophy,,,,,,,C1848736,,MTHU000679,,,
+BMGC_DS10970,BMG_DS039159,,Oliver-McFarlane syndrome,,,,,DOID:0111271,Oliver-McFarlane syndrome,C1848745,C536554,275400,MONDO:0010152,trichomegaly-retina pigmentary degeneration-dwarfism syndrome,
+BMGC_DS10971,BMG_DS039160,,"Tricarboxylic Acid Cycle, Defect of",,,,,,,C1848746,C564762,275370,MONDO:0010151,"tricarboxylic acid cycle, defect of",
+BMGC_DS10972,BMG_DS039161,,"TONGUE, PIGMENTED FUNGIFORM PAPILLAE OF",,,,,,,C1848756,,275250,MONDO:0010147,"tongue, pigmented fungiform papillae of",
+BMGC_DS10973,BMG_DS039164,,,,,,,,,C1848795,,275000,MONDO:0100489,"Graves disease, susceptibility to, 1",
+BMGC_DS10974,BMG_DS039165,,Thyroid Dyshormonogenesis 1,,,,,DOID:0112185,thyroid dyshormonogenesis 1,C1848805,C564766,274400,MONDO:0020716,thyroid dyshormonogenesis 1,
+BMGC_DS10975,BMG_DS039166,,Thymic-Renal-Anal-Lung dysplasia,,,,,,,C1848812,C536907,274265,MONDO:0010129,thymic-renal-anal-lung dysplasia,
+BMGC_DS10976,BMG_DS039167,,Thyrocerebral-retinal syndrome,,,,,,,C1848813,C536908,274240,MONDO:0010128,thyrocerebrorenal syndrome,
+BMGC_DS10977,BMG_DS039168,,,,,,,,,C1848814,,274230,MONDO:0010127,"thymoma, familial",
+BMGC_DS10978,BMG_DS039170,,"Thumb, Hypoplastic, with Choroid Coloboma, Poorly Developed Antihelix, and Deafness",,,,,,,C1848816,C564769,274205,MONDO:0010125,upper limb defect-eye and ear abnormalities syndrome,
+BMGC_DS10979,BMG_DS039171,,,,,,,,,C1848817,,274200,MONDO:0010124,"thumb, distal hyperextensibility of",
+BMGC_DS10980,BMG_DS039172,,"Thumb Agenesis, Short Stature, And Immunodeficiency",,,,,,,C1848818,C564770,274190,MONDO:0010123,obsolete absent thumb-short stature-immunodeficiency syndrome,
+BMGC_DS10981,BMG_DS039174,,,,,,,,,C1848861,,273770,MONDO:0010118,inherited threoninemia,
+BMGC_DS10982,BMG_DS039175,,Miller-McKusick-Malvaux-Syndrome (3M Syndrome),,,,,DOID:0060241,3-M syndrome,C1848862,C535314,,MONDO:0007477,3-M syndrome,
+BMGC_DS10983,BMG_DS039176,,Thoracomelic Dysplasia,,,,,,,C1848863,C564773,273740,MONDO:0010116,thoracomelic dysplasia,
+BMGC_DS10984,BMG_DS039178,,Thanatophoric dysplasia Glasgow variant,,,,,,,C1848865,C536506,273680,MONDO:0010114,"thanatophoric dysplasia, Glasgow variant",
+BMGC_DS10985,BMG_DS039179,,,,,,,,,C1848901,,273150,MONDO:0010106,"testes, rudimentary",
+BMGC_DS10986,BMG_DS039180,,,,,,,,,C1848902,,273120,MONDO:0010105,"teratoma, pineal",
+BMGC_DS10987,BMG_DS039183,771265006,Teebi Shaltout syndrome,,,,,,,C1848912,C536950,272950,MONDO:0010101,Teebi-Shaltout syndrome,Teebi Shaltout syndrome | Teebi Shaltout syndrome (disorder)
+BMGC_DS10988,BMG_DS039184,,"Tay-Sachs Disease, Juvenile",,,,,,,C1848913,C564782,,,,
+BMGC_DS10989,BMG_DS039185,,"Hexosaminidase A Deficiency, Adult Type",,,,,,,C1848914,C564783,,MONDO:0017726,"Tay-Sachs disease, B variant, adult form",
+BMGC_DS10990,BMG_DS039187,,"Tay-Sachs Disease, Variant B1",,,,,,,C1848916,C564785,,MONDO:0017728,"Tay-Sachs disease, B1 variant",
+BMGC_DS10991,BMG_DS039189,,Hexosaminidase alpha-Subunit Deficiency (Variant B),Tay-Sachs Disease,,,,,,C1848922,D013661,,,,
+BMGC_DS10992,BMG_DS039190,,Tatsumi Factor Deficiency,,,,,,,C1848931,C564787,272650,MONDO:0010097,Tatsumi factor deficiency,
+BMGC_DS10993,BMG_DS039192,,SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME,,,,,,,C1848934,,603381;272460,MONDO:0010094,spondylocarpotarsal synostosis syndrome,
+BMGC_DS10994,BMG_DS039193,,,,,,,,,C1848947,,272430;601378,MONDO:0010091,Cold-induced sweating syndrome 1,
+BMGC_DS10995,BMG_DS039194,,,,,,,,,C1848954,,,MONDO:0000476,generalized dystonia,
+BMGC_DS10996,BMG_DS039195,,"Sucrosuria, Hiatus Hernia and Mental Retardation",,,,,,,C1848963,C564792,272000,MONDO:0010084,"sucrosuria, hiatus hernia and intellectual disability",
+BMGC_DS10997,BMG_DS039197,,"SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE",,,,,DOID:0112196,"spondylometaepiphyseal dysplasia, short limb-hand type",C1849011,,191311;271665,MONDO:0010077,spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome,
+BMGC_DS10998,BMG_DS039198,,"Spondyloepiphyseal dysplasia tarda, Toledo type",,,,,,,C1849048,C535787,271630,MONDO:0010074,"brachyolmia type 1, toledo type",
+BMGC_DS10999,BMG_DS039199,,Spondyloepiphyseal Dysplasia Tarda with Mental Retardation,,,,,DOID:0112292,spondyloepiphyseal dysplasia tarda with intellectual disability,C1849053,C564796,271620,MONDO:0010073,"spondyloepiphyseal dysplasia tarda, Kohn type",
+BMGC_DS11000,BMG_DS039200,,"Spondyloepiphyseal Dysplasia Tarda, Autosomal Recessive",,,,,,,C1849054,C564797,271600,MONDO:0010072,"spondyloepiphyseal dysplasia tarda, autosomal recessive",
+BMGC_DS11001,BMG_DS039201,,"Brachyolmia, recessive Hobaek type",,,,,,,C1849055,C537099,271530,MONDO:0010070,"brachyolmia type 1, Hobaek type",
+BMGC_DS11002,BMG_DS039202,,Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies,,,,,,,C1849069,C564799,271520,MONDO:0010069,spondylocostal dysostosis-anal and genitourinary malformations syndrome,
+BMGC_DS11003,BMG_DS039203,,Mousa Al din Al Nassar syndrome,,,,,,,C1849085,C536989,271320,MONDO:0010064,spastic ataxia-corneal dystrophy syndrome,
+BMGC_DS11004,BMG_DS039204,720750004,Corneal cerebellar syndrome,,,,,,,C1849087,C535472,271310,MONDO:0010063,corneal-cerebellar syndrome,Spinocerebellar degeneration and corneal dystrophy syndrome (disorder) | Corneal cerebellar syndrome | Der Kaloustian Jarudi Khoury syndrome | Spinocerebellar degeneration and corneal dystrophy syndrome
+BMGC_DS11005,BMG_DS039206,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 3",,,,,DOID:0111612,autosomal recessive spinocerebellar ataxia 3,C1849094,,271250,MONDO:0010061,autosomal recessive cerebellar ataxia-blindness-deafness syndrome,
+BMGC_DS11006,BMG_DS039207,724227000,Infantile onset spinocerebellar ataxia,,,,,DOID:0080126,mitochondrial DNA depletion syndrome 7,C1849096,C535523,271245,MONDO:0010060,mitochondrial DNA depletion syndrome 7 (hepatocerebral type),"Infantile onset spinocerebellar ataxia (disorder) | Infantile onset spinocerebellar ataxia | Ohaha syndrome | Ophthalmoplegia, hypotonia, ataxia, hypoacusis, athetosis syndrome"
+BMGC_DS11007,BMG_DS039209,,"Spinal muscular atrophy, Ryukyuan type",,,,,,,C1849102,C536881,271200,MONDO:0010057,"spinal muscular atrophy, Ryukyuan type",
+BMGC_DS11008,BMG_DS039211,,Spinal Muscular Atrophy with Mental Retardation,,,,,,,C1849109,C564807,271109,MONDO:0010054,spinal muscular atrophy with intellectual disability,
+BMGC_DS11009,BMG_DS039212,,"Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation",,,,,,,C1849112,C564808,270950,MONDO:0010051,spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome,
+BMGC_DS11010,BMG_DS039213,,"Spastic Paresis, Glaucoma, and Mental Retardation",,,,,,,C1849113,C564809,270850,MONDO:0010049,spastic paraplegia-glaucoma-intellectual disability syndrome,
+BMGC_DS11011,BMG_DS039215,,"Spastic Paraplegia 5a, Autosomal Recessive",,,,,,,C1849115,C564811,270800,MONDO:0010047,hereditary spastic paraplegia 5A,
+BMGC_DS11012,BMG_DS039216,,"Spastic paraplegia 15, autosomal recessive",,,,,,,C1849128,C536642,270700,MONDO:0010044,hereditary spastic paraplegia 15,
+BMGC_DS11013,BMG_DS039217,,Spastic diplegia infantile type,,,,,,,C1849139,C537481,270600,MONDO:0010042,spastic diplegia and intellectual disability,
+BMGC_DS11014,BMG_DS039218,,"SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE",,,,,,,C1849140,,604490;270550,MONDO:0010041,Charlevoix-Saguenay spastic ataxia,
+BMGC_DS11015,BMG_DS039219,,Spastic Ataxia,,,,,DOID:0050952,spastic ataxia,C1849156,C564815,,MONDO:0017845,spastic ataxia,
+BMGC_DS11016,BMG_DS039220,,"Insulin-Like Growth Factor I, Resistance To",,,,,,,C1849157,C564816,270450,MONDO:0010038,growth delay due to insulin-like growth factor I resistance,
+BMGC_DS11017,BMG_DS039222,,,,,,,,,C1849169,,270425,MONDO:0010037,sodium-potassium-ATPase activity of red cell,
+BMGC_DS11018,BMG_DS039223,,,,,,,DOID:0060283,peeling skin syndrome,C1849193,,270300,MONDO:0024548,peeling skin syndrome 1,
+BMGC_DS11019,BMG_DS039226,,"Severe combined immunodeficiency, atypical",,,,,DOID:0111943,immunodeficiency 48,C1849236,C537590,,,,
+BMGC_DS11020,BMG_DS039229,,Second Metatarsal-Metacarpal Syndrome,,,,,,,C1849259,C564824,269630,MONDO:0010018,second metatarsal-metacarpal syndrome,
+BMGC_DS11021,BMG_DS039230,,Rodrigues blindness,,,,,,,C1849332,C535865,268320,MONDO:0010001,ectodermal dysplasia-blindness syndrome,
+BMGC_DS11022,BMG_DS039231,,"Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction",,,,,,,C1849333,C564829,268315,MONDO:0010000,"rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction",
+BMGC_DS11023,BMG_DS039232,,"Robinow syndrome, autosomal recessive",,,,,,,C1849334,C535863,,,,
+BMGC_DS11024,BMG_DS039233,723998001,Richieri Costa Pereira syndrome,,,,,,,C1849348,C535677,268305,MONDO:0009998,Richieri Costa-Pereira syndrome,"Robin sequence with cleft mandible and limb anomalies syndrome | Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome (disorder) | Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome | Richieri Costa Pereira syndrome"
+BMGC_DS11025,BMG_DS039234,,Rhizomelic syndrome,,,,,,,C1849382,C537611,268250,MONDO:0009996,"rhizomelic syndrome, Urbach type",
+BMGC_DS11026,BMG_DS039235,,"Myoglobinuria, Acute Recurrent, Autosomal Recessive",,,,,,,C1849386,C564832,268200,MONDO:0009992,"myoglobinuria, acute recurrent, autosomal recessive",
+BMGC_DS11027,BMG_DS039236,,"Rh-Null, Regulator Type",,,,,,,C1849387,C564833,,,,
+BMGC_DS11028,BMG_DS039237,,Enhanced S-Cone Syndrome,,,,,DOID:0090059,enhanced S-cone syndrome,C1849394,C564835,268100,MONDO:0100288,enhanced S-cone syndrome,
+BMGC_DS11029,BMG_DS039239,,"Retinopathy, Pericentral Pigmentary, Autosomal Recessive",,,,,,,C1849398,C564838,268060,MONDO:0009987,autosomal recessive pericentral pigmentary retinopathy,
+BMGC_DS11030,BMG_DS039241,,"Retinitis Pigmentosa, Late-Adult Onset",,,,,,,C1849400,C564840,268025,MONDO:0009984,late-adult onset retinitis pigmentosa,
+BMGC_DS11031,BMG_DS039242,,"Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism",,,,,,,C1849401,C564841,268020,MONDO:0009983,retinitis pigmentosa-intellectual disability-deafness-hypogenitalism syndrome,
+BMGC_DS11032,BMG_DS039245,703542000,Knobloch syndrome,,,,,,,C1849409,C537209,,MONDO:0800166,Knobloch syndrome,Retinal detachment and occipital encephalocele | Knobloch syndrome | Retinal detachment and occipital encephalocoele | Retinal detachment and occipital encephalocele (disorder)
+BMGC_DS11033,BMG_DS039246,,Retinal Degeneration and Epilepsy,,,,,,,C1849416,C564847,267740,MONDO:0009976,retinal degeneration and epilepsy,
+BMGC_DS11034,BMG_DS039248,,"Renal, Genital, and Middle Ear Anomalies",,,,,,,C1849432,C564849,267400,MONDO:0009969,renal-genital-middle ear anomalies,
+BMGC_DS11035,BMG_DS039249,,"Renal tubular acidosis, distal, type 3",,,,,,,C1849435,C537759,267200,MONDO:0009967,renal tubular acidosis 3,
+BMGC_DS11036,BMG_DS039250,,Mainzer-Saldino Disease,,,,,,,C1849437,C535463,266920,MONDO:0009964,short-rib thoracic dysplasia 9 with or without polydactyly,
+BMGC_DS11037,BMG_DS039253,,Reese Retinal Dysplasia,,,,,,,C1849450,C564854,266400,MONDO:0009957,Reese retinal dysplasia,
+BMGC_DS11038,BMG_DS039254,,Red skin pigment anomaly of New Guinea,,,,,,,C1849451,C535515,266350,MONDO:0009956,red skin pigment anomaly of new guinea,
+BMGC_DS11039,BMG_DS039255,,Rapadilino syndrome,,,,,DOID:0050774,rapadilino syndrome,C1849453,C535288,266280,MONDO:0009955,rapadilino syndrome,
+BMGC_DS11040,BMG_DS039256,,"Radioulnar Synostosis, Unilateral, with Developmental Retardation and Hypotonia",,,,,,,C1849470,C564856,266255,MONDO:0009952,radioulnar synostosis-developmental delay-hypotonia syndrome,
+BMGC_DS11041,BMG_DS039257,,"Radiculoneuropathy, Fatal Neonatal",,,,,,,C1849471,C564857,266250,MONDO:0009951,"radiculoneuropathy, fatal neonatal",
+BMGC_DS11042,BMG_DS039258,,"Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to",,,,,,,C1849507,C564859,266120,MONDO:0009946,hemolytic anemia due to pyrimidine 5' nucleotidase deficiency,
+BMGC_DS11043,BMG_DS039259,,"EPILEPSY, PYRIDOXINE-DEPENDENT",,,,,DOID:0070519;DOID:0080768,early-onset vitamin B6-dependent epilepsy 4 | pyridoxine-dependent epilepsy,C1849508,,266100,MONDO:0009945,pyridoxine-dependent epilepsy,
+BMGC_DS11044,BMG_DS039260,719258003,Pyknoachondrogenesis,,,,,,,C1849523,C536251,265880,MONDO:0009942,pyknoachondrogenesis,Pyknoachondrogenesis (disorder) | Pyknoachondrogenesis | Camera syndrome
+BMGC_DS11045,BMG_DS039262,,,,,,,,,C1849554,,265300,MONDO:0009933,congenital pulmonary lymphangiectasia,
+BMGC_DS11046,BMG_DS039263,,Pulmonary Bullae Causing Pneumothorax,,,,,,,C1849566,C564863,265200,MONDO:0009932,pulmonary bullae causing pneumothorax,
+BMGC_DS11047,BMG_DS039264,,Pseudouridinuria and Mental Defect,,,,,,,C1849648,C564864,264500,MONDO:0009922,Pseudouridinuria and mental defect,
+BMGC_DS11048,BMG_DS039265,716091000,Pseudotrisomy 13 syndrome,,,,,,,C1849649,C535829,264480,MONDO:0009921,holoprosencephaly-postaxial polydactyly syndrome,Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Holoprosencephaly and postaxial polydactyly syndrome | Pseudotrisomy 13 syndrome
+BMGC_DS11049,BMG_DS039268,,Peroxisomal ACYL-COA oxidase deficiency,,,,,DOID:0050797,peroxisomal acyl-CoA oxidase deficiency,C1849678,C536662,264470,MONDO:0009919,peroxisomal acyl-CoA oxidase deficiency,
+BMGC_DS11050,BMG_DS039269,,"Fundus dystrophy, pseudoinflammatory recessive form",,,,,,,C1849694,C535828,264420,MONDO:0009918,"fundus dystrophy, pseudoinflammatory, recessive form",
+BMGC_DS11051,BMG_DS039271,,"Pseudohermaphroditism, Female, with Skeletal Anomalies",,,,,,,C1849696,C564869,264270,MONDO:0009915,"46,XX disorder of sex development-skeletal anomalies syndrome",
+BMGC_DS11052,BMG_DS039272,,Prolactin Deficiency with Obesity and Enlarged Testes,,,,,,,C1849698,C564870,264120,MONDO:0009912,prolactin deficiency with obesity and enlarged testes,
+BMGC_DS11053,BMG_DS039273,,Progesterone Resistance,,,,,,,C1849699,C564871,264080,MONDO:0009909,progesterone resistance,
+BMGC_DS11054,BMG_DS039274,,Hyperphenylalaninemia with primapterinuria,,,,,,,C1849700,C538382,264070,MONDO:0009908,pterin-4 alpha-carbinolamine dehydratase 1 deficiency,
+BMGC_DS11055,BMG_DS039275,,,,,,,,,C1849701,,264050,MONDO:0009906,prenatal bowing,
+BMGC_DS11056,BMG_DS039276,,"POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE",,,,,,,C1849718,,263650,MONDO:0009901,Bartsocas-Papas syndrome 1,
+BMGC_DS11057,BMG_DS039277,,Bonneau Syndrome,,,,,,,C1849719,C564875,263630,MONDO:0009900,polysyndactyly-cardiac malformation syndrome,
+BMGC_DS11058,BMG_DS039278,,"Polyhydramnios, Chronic Idiopathic",,,,,,,C1849720,C564876,263610,MONDO:0009899,"polyhydramnios, chronic idiopathic",
+BMGC_DS11059,BMG_DS039279,,,,,,,,,C1849721,,263600,MONDO:0009898,"polysaccharide, storage of unusual",
+BMGC_DS11060,BMG_DS039280,,"Polyglucosan Body Disease, Adult Form",,,,,,,C1849722,C564878,263570,MONDO:0009897,adult polyglucosan body disease,
+BMGC_DS11061,BMG_DS039281,,Infantile polymyoclonus,,,,,,,C1849731,C535524,263550,MONDO:0009896,"polymyoclonus, infantile",
+BMGC_DS11062,BMG_DS039283,,"Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia",,,,,,,C1849762,C564881,263210,MONDO:0009890,Gillessen-Kaesbach-Nishimura syndrome,
+BMGC_DS11063,BMG_DS039284,870517000,Periportal fibrosis,,,,,,,C1849766,,MTHU010078,,,Periportal fibrosis | Periportal fibrosis (disorder)
+BMGC_DS11064,BMG_DS039287,,Platelet Prostacyclin Receptor Defect,,,,,,,C1849774,C564884,262875,MONDO:0009884,platelet prostacyclin receptor defect,
+BMGC_DS11065,BMG_DS039289,,Kowarski syndrome,,,,,,,C1849779,C537505,262650,MONDO:0009879,short stature due to growth hormone qualitative anomaly,
+BMGC_DS11066,BMG_DS039290,,Achromatopsia 3,,,,,DOID:0110008,achromatopsia 3,C1849792,C536129,262300,MONDO:0009875,achromatopsia 3,
+BMGC_DS11067,BMG_DS039292,,Pili torti developmental delay neurological abnormalities,,,,,,,C1849811,C537398,261990,MONDO:0009871,pili torti-developmental delay-neurological abnormalities syndrome,
+BMGC_DS11068,BMG_DS039293,,"Glycogen Storage Disease of Heart, Lethal Congenital",,,,,,,C1849813,C564888,261740,MONDO:0009867,lethal congenital glycogen storage disease of heart,
+BMGC_DS11069,BMG_DS039294,,"Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial",,,,,,,C1849821,C564890,261650,MONDO:0009864,"phosphoenolpyruvate carboxykinase deficiency, mitochondrial",
+BMGC_DS11070,BMG_DS039295,,,,,,,,,C1849927,,261590,MONDO:0009860,phenformin 4-hydroxylation,
+BMGC_DS11071,BMG_DS039298,,,,,,,DOID:0050791,persistent Mullerian duct syndrome,C1849930,,261550,MONDO:0009857,persistent Mullerian duct syndrome,
+BMGC_DS11072,BMG_DS039299,,Presentey Anomaly,,,,,,,C1850000,C564893,261500,MONDO:0043364,eosinophil peroxidase deficiency,
+BMGC_DS11073,BMG_DS039300,,,,,,,,,C1850001,,261400,MONDO:0009854,"peroneus tertius muscle, absence of",
+BMGC_DS11074,BMG_DS039301,,"Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain",,,,,,,C1850022,C564894,260970,MONDO:0009851,"peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and spongy degeneration of brain",
+BMGC_DS11075,BMG_DS039303,719299009,Pelviscapular dysplasia,,,,,,,C1850040,C535550,260660,MONDO:0009845,pelviscapular dysplasia,Pelviscapular dysplasia | Cousin syndrome | Familial pelvis-scapular dysplasia | Pelviscapular dysplasia syndrome (disorder) | Pelviscapular dysplasia syndrome
+BMGC_DS11076,BMG_DS039305,,"Pelizaeus-Merzbacher-like disease, autosomal recessive, 2",,,,,,,C1850053,C536319,260600,MONDO:0009843,hypomyelinating leukodystrophy 3,
+BMGC_DS11077,BMG_DS039306,,Pelger-Huet-Like Anomaly and Episodic Fever with Abdominal Pain,,,,,,,C1850054,C564899,260570,MONDO:0009842,Pelger-Huet-like anomaly and episodic fever with abdominal pain,
+BMGC_DS11078,BMG_DS039307,442511009,PEHO syndrome,,,,,DOID:0080539,PEHO syndrome,C1850055,C536317,260565,MONDO:0009841,PEHO syndrome,"Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy syndrome | Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome (disorder) | PEHO syndrome | PEHO (progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy) syndrome | PEHO (progressive encephalopathy with edema, hypsarrhythmia and optic atrophy) syndrome"
+BMGC_DS11079,BMG_DS039308,770678005,"Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome",,,,,,,C1850056,,617507,MONDO:0020495,PEHO-like syndrome,"PEHO-like syndrome | Progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like syndrome | Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (disorder) | Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome | PEHOL (progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like) syndrome | PEHOL (progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like) syndrome"
+BMGC_DS11080,BMG_DS039310,,"Supranuclear Palsy, Progressive, 1, Atypical",,,,,,,C1850077,C537240,260540,MONDO:0009839,progressive supranuclear palsy-parkinsonism syndrome,
+BMGC_DS11081,BMG_DS039311,,Parana Hard Skin Syndrome,,,,,,,C1850079,C564905,260530,MONDO:0009838,Parana hard-skin syndrome,
+BMGC_DS11082,BMG_DS039314,,"Pancreatic Agenesis, Congenital",,,,,,,C1850096,C564908,,,,
+BMGC_DS11083,BMG_DS039315,783012006,Pallidopyramidal syndrome,,,,,,,C1850100,C538104,260300,MONDO:0009830,parkinsonian-pyramidal syndrome,Parkinsonian pyramidal syndrome (disorder) | Pallidopyramidal syndrome | Parkinsonian pyramidal syndrome
+BMGC_DS11084,BMG_DS039319,,,,,,,,,C1850104,,260100,MONDO:0009826,PA polymorphism of alpha-2-globulin,
+BMGC_DS11085,BMG_DS039320,,Otoonychoperoneal Syndrome,,,,,,,C1850105,C564912,259780,MONDO:0009822,otoonychoperoneal syndrome,
+BMGC_DS11086,BMG_DS039321,,RAINE SYNDROME,,,,,,,C1850106,,611061;259775;259660;259775,MONDO:0009821,lethal osteosclerotic bone dysplasia,
+BMGC_DS11087,BMG_DS039322,,"Osteopetrosis, mild autosomal recessive form",,,,,,,C1850126,C536059,259710,MONDO:0009816,autosomal recessive osteopetrosis 2,
+BMGC_DS11088,BMG_DS039323,,"Osteopetrosis, Autosomal Recessive 1",,,,,,,C1850127,C564915,259700,MONDO:0009815,autosomal recessive osteopetrosis 1,
+BMGC_DS11089,BMG_DS039324,732954002,Kaler Garrity Stern syndrome,,,,,,,C1850140,C537706,259690,MONDO:0009814,osteopenia-intellectual disability-sparse hair syndrome,"Osteopenia, intellectual disability, sparse hair syndrome (disorder) | Kaler Garrity Stern syndrome | Osteopenia, intellectual disability, sparse hair syndrome"
+BMGC_DS11090,BMG_DS039325,,,,,,,,,C1850142,,259650,MONDO:0009811,osteoma of middle ear,
+BMGC_DS11091,BMG_DS039327,,,,,,,,,C1850155,,,MONDO:0018298,multicentric osteolysis-nodulosis-arthropathy spectrum,
+BMGC_DS11092,BMG_DS039328,,Bruck syndrome 1,,,,,,,C1850168,C537406,259450,MONDO:0009806,Bruck syndrome 1,
+BMGC_DS11093,BMG_DS039329,,"Osteogenesis Imperfecta, Type IX",,,,,,,C1850169,C564921,259440,MONDO:0009805,osteogenesis imperfecta type 9,
+BMGC_DS11094,BMG_DS039330,,"Osteogenesis imperfecta congenita, microcephaly, and cataracts",,,,,,,C1850184,C537558,259410,MONDO:0009803,congenital osteogenesis imperfecta-microcephaly-cataracts syndrome,
+BMGC_DS11095,BMG_DS039331,,"Osteodysplasty, Precocious, Of Danks, Mayne, And Kozlowski",,,,,,,C1850185,C564922,259270,MONDO:0009802,"osteodysplasty, precocious, of Danks, Mayne, and Kozlowski",
+BMGC_DS11096,BMG_DS039334,,,,,,,,,C1850269,,258800,MONDO:0009791,"oral sensibility, disturbance of",
+BMGC_DS11097,BMG_DS039335,,Optic atrophy 6,,,,,DOID:0111435,optic atrophy 6,C1850281,C537127,258500,MONDO:0009786,optic atrophy 6,
+BMGC_DS11098,BMG_DS039336,,Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria,,,,,,,C1850302,C564925,258470,MONDO:0009784,ophthalmoplegic neuromuscular disorder with abnormal mitochondria,
+BMGC_DS11099,BMG_DS039337,,,,,,,,,C1850303,,,MONDO:0016810,autosomal recessive progressive external ophthalmoplegia,
+BMGC_DS11100,BMG_DS039338,,Ophthalmoplegia Totalis with Ptosis and Miosis,,,,,,,C1850314,C564927,258400,MONDO:0009782,ophthalmoplegia totalis with ptosis and miosis,
+BMGC_DS11101,BMG_DS039339,,Onychotrichodysplasia and neutropenia,,,,,,,C1850316,C537752,258360,MONDO:0009781,Onychotrichodysplasia and neutropenia,
+BMGC_DS11102,BMG_DS039340,,Omphalocele cleft palate syndrome lethal,,,,,,,C1850317,C537747,258320,MONDO:0009780,lethal omphalocele-cleft palate syndrome,
+BMGC_DS11103,BMG_DS039341,,Omodysplasia type 1,,,,,DOID:0080844,omodysplasia 1,C1850318,C537746,258315,MONDO:0009779,autosomal recessive omodysplasia,
+BMGC_DS11104,BMG_DS039343,,Oliver Syndrome,,,,,,,C1850320,C564931,258200,MONDO:0009777,Oliver syndrome,
+BMGC_DS11105,BMG_DS039344,,,,,,,,,C1850321,,258040,MONDO:0017919,exstrophy-epispadias complex,
+BMGC_DS11106,BMG_DS039345,1208341008,Oculorenocerebellar syndrome,,,,,,,C1850331,C537739,257970,MONDO:0009772,oculorenocerebellar syndrome,Severe oculo-renal-cerebellar syndrome (disorder) | Hunter Jurenka Thompson syndrome | Oculorenocerebellar syndrome | Severe oculo-renal-cerebellar syndrome | ORC (oculo-renal-cerebellar) syndrome
+BMGC_DS11107,BMG_DS039347,,Oculopalatocerebral Syndrome,,,,,,,C1850338,C564935,257910,MONDO:0009769,oculo-palato-cerebral syndrome,
+BMGC_DS11108,BMG_DS039349,,Mosaic variegated aneuploidy syndrome 1,,,,,DOID:0080688,mosaic variegated aneuploidy syndrome,C1850343,C536987,257300,MONDO:0009759,mosaic variegated aneuploidy syndrome 1,
+BMGC_DS11109,BMG_DS039350,,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B",,,,,DOID:0110865,congenital stationary night blindness 1B,C1850362,,257270;604096,MONDO:0009758,congenital stationary night blindness 1B,
+BMGC_DS11110,BMG_DS039352,,NEUTROPHIL ACTIN DYSFUNCTION,,,,,,,C1850380,,257150,MONDO:0009755,neutrophil actin dysfunction,
+BMGC_DS11111,BMG_DS039353,,"Neutropenia, Lethal Congenital, with Eosinophilia",,,,,,,C1850381,C564943,257100,MONDO:0009754,"neutropenia, lethal congenital, with eosinophilia",
+BMGC_DS11112,BMG_DS039355,,"Neuropathy, Painful",,,,,,,C1850383,C564945,256870,MONDO:0009752,"neuropathy, painful",
+BMGC_DS11113,BMG_DS039358,,GIANT AXONAL NEUROPATHY 1,,,,,,,C1850386,,605379;256850,MONDO:0009749,giant axonal neuropathy 1,
+BMGC_DS11114,BMG_DS039360,,"Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive",,,,,,,C1850395,C564948,256840,MONDO:0009748,hereditary sensory and autonomic neuropathy with spastic paraplegia,
+BMGC_DS11115,BMG_DS039361,,NAVAJO NEUROHEPATOPATHY,,,,,,,C1850406,,256810,MONDO:0009747,mitochondrial DNA depletion syndrome 6 (hepatocerebral type),
+BMGC_DS11116,BMG_DS039362,,Navajo Familial Neurogenic Arthropathy,,,,,DOID:0080125,mitochondrial DNA depletion syndrome 6,C1850407,C538344,,,,
+BMGC_DS11117,BMG_DS039363,,"CEROID LIPOFUSCINOSIS, NEURONAL, 5",,,,,,,C1850442,,256731;608102,MONDO:0009745,neuronal ceroid lipofuscinosis 5,
+BMGC_DS11118,BMG_DS039364,,"CEROID LIPOFUSCINOSIS, NEURONAL, 1",,,,,,,C1850451,,600722;256730;256730;214200,MONDO:0009744,neuronal ceroid lipofuscinosis 1,
+BMGC_DS11119,BMG_DS039367,,Nephrosis deafness urinary tract digital malformation,,,,,,,C1850552,C536402,256200,MONDO:0009731,nephrosis-deafness-urinary tract-digital malformations syndrome,
+BMGC_DS11120,BMG_DS039369,254055004,Atelosteogenesis type 2,,,,,,,C1850554,C535395,256050,MONDO:0009727,atelosteogenesis type II,Atelosteogenesis type 2 | Atelosteogenesis de la Chapelle type | Atelosteogenesis type 2 (disorder)
+BMGC_DS11121,BMG_DS039370,,De La Chapelle Dysplasia,,,,,,,C1850555,C535395,,MONDO:0800307,de la Chapelle dysplasia,
+BMGC_DS11122,BMG_DS039371,702449004,Nakajo syndrome,,,,,,,C1850568,C538334,,MONDO:0009726,proteosome-associated autoinflammatory syndrome,"Autoinflammation, lipodystrophy and dermatosis syndrome | Japanese autoinflammatory syndrome with lipodystrophy | Nakajo-Nishimura syndrome | Nakajo syndrome | Autoinflammation, lipodystrophy and dermatosis syndrome (disorder) | Proteasome-associated autoinflammatory syndrome"
+BMGC_DS11123,BMG_DS039372,,Nemaline Myopathy 2,,,,,DOID:0110928,nemaline myopathy 2,C1850569,C538349,256030,MONDO:0009725,nemaline myopathy 2,
+BMGC_DS11124,BMG_DS039375,,Leigh Syndrome due to Mitochondrial Complex IV Deficiency,,,,,,,C1850599,C564963,,,,
+BMGC_DS11125,BMG_DS039377,723439002,Native American myopathy,,,,,DOID:0060346,Native American myopathy,C1850625,C538343,255995,MONDO:0009722,Bailey-Bloch congenital myopathy,"Congenital myopathy, cleft palate. malignant hyperthermia syndrome | Native American myopathy | Native American myopathy (disorder)"
+BMGC_DS11126,BMG_DS039378,716170005,Nathalie syndrome,,,,,,,C1850626,C538342,255990,MONDO:0009721,Nathalie syndrome,Deafness with cataract and skeletal anomaly syndrome (disorder) | Deafness with cataract and skeletal anomaly syndrome | Nathalie syndrome
+BMGC_DS11127,BMG_DS039379,763774001,Nasodigitoacoustic syndrome,,,,,DOID:0111842,Keipert syndrome,C1850627,C538337,255980;301026,MONDO:0009720,Keipert syndrome,Keipert syndrome (disorder) | Nasodigitoacoustic syndrome | Keipert syndrome
+BMGC_DS11128,BMG_DS039381,,"Myosclerosis, Autosomal Recessive",,,,,,,C1850671,C564968,255600,MONDO:0009714,myosclerosis,
+BMGC_DS11129,BMG_DS039382,,Minicore Myopathy with External Ophthalmoplegia,,,,,,,C1850674,C564969,255320,MONDO:0009712,congenital multicore myopathy with external ophthalmoplegia,
+BMGC_DS11130,BMG_DS039383,,"Myopathy, Hyaline Body, Autosomal Recessive",,,,,,,C1850709,C564970,255160,MONDO:0009708,"myopathy, myosin storage, autosomal recessive",
+BMGC_DS11131,BMG_DS039385,,"MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE",,,,,,,C1850718,,255125,MONDO:0009706,hereditary myopathy with lactic acidosis due to ISCU deficiency,
+BMGC_DS11132,BMG_DS039387,,"Myopathy, Granulovacuolar Lobular, with Electrical Myotonia",,,,,,,C1850745,C564974,254950,MONDO:0009701,"myopathy, granulovacuolar lobular, with electrical myotonia",
+BMGC_DS11133,BMG_DS039388,,"Myopathy, congenital nonprogressive with Moebius and Robin sequences",,,,,,,C1850746,C536102,,MONDO:0031415,Carey-Fineman-Ziter syndrome,
+BMGC_DS11134,BMG_DS039391,,,,,,,,,C1850764,,620681,MONDO:0800306,myoclonic epilepsy of Lafora 2,
+BMGC_DS11135,BMG_DS039392,,,,,,,,,C1850778,,,MONDO:0020752,"myoclonic epilepsy, juvenile, susceptibility to, 1",
+BMGC_DS11136,BMG_DS039393,,"Myeloproliferative Disease, Autosomal Recessive",,,,,,,C1850779,C564977,254700,MONDO:0009695,"myeloproliferative disease, autosomal recessive",
+BMGC_DS11137,BMG_DS039394,,Congenital myasthenic syndrome ib,,,,,,,C1850792,C536089,609456;254300,MONDO:0009690,congenital myasthenic syndrome 10,
+BMGC_DS11138,BMG_DS039395,,"Myasthenia, Congenital, Refractory to Acetylcholinesterase Inhibitors",,,,,,,C1850806,C564979,254190,MONDO:0009687,"myasthenia, congenital, refractory to acetylcholinesterase inhibitors",
+BMGC_DS11139,BMG_DS039396,,"Musk, Inability to Smell",,,,,,,C1850807,C564980,254150,MONDO:0009686,"musk, inability to smell",
+BMGC_DS11140,BMG_DS039397,,"Muscular Hypertonia, Lethal",,,,,,,C1850827,C564982,254120,MONDO:0009684,"muscular hypertonia, lethal",
+BMGC_DS11141,BMG_DS039398,,"Muscular Dystrophy, Congenital, with Rapid Progression",,,,,,,C1850840,C564983,254100,MONDO:0009682,"muscular dystrophy, congenital, with rapid progression",
+BMGC_DS11142,BMG_DS039399,,"Muscular dystrophy, congenital, infantile with cataract and hypogonadism",,,,,,,C1850864,C537385,254000,MONDO:0009680,congenital muscular dystrophy-infantile cataract-hypogonadism syndrome,
+BMGC_DS11143,BMG_DS039401,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B",,,,,,,C1850889,,253601,MONDO:0009676,autosomal recessive limb-girdle muscular dystrophy type 2B,
+BMGC_DS11144,BMG_DS039402,782946000,Gastrocutaneous syndrome,,,,,,,C1850899,C535651,137270,MONDO:0007651,gastrocutaneous syndrome,Gastrocutaneous syndrome | Gastrocutaneous syndrome (disorder)
+BMGC_DS11145,BMG_DS039405,,"Gamma-A-Globulin, Defect in Assembly of",,,,,,,C1850934,C564991,137050,MONDO:0007643,"gamma-A-globulin, defect in assembly of",
+BMGC_DS11146,BMG_DS039406,,"FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, OF SORSBY",,,,,DOID:0090114,Sorsby's fundus dystrophy,C1850938,,136900,MONDO:0007640,Sorsby fundus dystrophy,
+BMGC_DS11147,BMG_DS039408,,"Corneal dystrophy, Fuchs' endothelial, 1",,,,,,,C1850959,C535478,136800,MONDO:0007637,"corneal dystrophy, Fuchs endothelial, 1",
+BMGC_DS11148,BMG_DS039412,,"Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness",,,,,,,C1850982,C564999,136600,MONDO:0007633,"Friedreich ataxia, so-called, with optic atrophy and sensorineural deafness",
+BMGC_DS11149,BMG_DS039417,,"fourth cranial nerve palsy, familial congenital",,,,,,,C1850996,C565007,136480,MONDO:0007626,familial congenital palsy of trochlear nerve,
+BMGC_DS11150,BMG_DS039421,,"FINGER LOCKING, RECURRENT, WITH INTRAUTERINE GROWTH RETARDATION AND PROPORTIONATE SHORT STATURE",,,,,,,C1851081,,135950,MONDO:0007618,Eng-Strom syndrome,
+BMGC_DS11151,BMG_DS039423,,LAURIN-SANDROW SYNDROME,,,,,DOID:0111350,Laurin-Sandrow syndrome,C1851100,,135750;605522,MONDO:0007615,laurin-Sandrow syndrome,
+BMGC_DS11152,BMG_DS039424,,"Laurin-Sandrow Syndrome, Segmental",,,,,,,C1851101,C535689,,,,
+BMGC_DS11153,BMG_DS039425,,"Fibrosis Of Extraocular Muscles, Congenital, 1",,,,,,,C1851102,C567739,135700,MONDO:0021083,congenital fibrosis of extraocular muscles type 1,
+BMGC_DS11154,BMG_DS039426,722449007,Jones syndrome,,,,,,,C1851112,C535886,135550,MONDO:0007612,gingival fibromatosis-progressive deafness syndrome,Gingival fibromatosis with progressive deafness syndrome (disorder) | Gingival fibromatosis with progressive deafness syndrome | Jones syndrome
+BMGC_DS11155,BMG_DS039427,,"Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia",,,,,,,C1851120,C565016,135400,MONDO:0007610,gingival fibromatosis-hypertrichosis syndrome,
+BMGC_DS11156,BMG_DS039428,,"Desmoid disease, hereditary",,,,,DOID:0111349,hereditary desmoid disease,C1851124,C535944,,,,
+BMGC_DS11157,BMG_DS039429,,SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS,,,,,,,C1851152,,134934,,,
+BMGC_DS11158,BMG_DS039430,,Fibrinolytic Defect,,,,,,,C1851184,C565017,134900,MONDO:0007605,fibrinolytic defect,
+BMGC_DS11159,BMG_DS039432,,Ectopia lentis isolated,,,,,DOID:0111150,autosomal dominant isolated ectopia lentis 1,C1851286,C536184,,MONDO:0015998,isolated ectopia lentis,
+BMGC_DS11160,BMG_DS039433,,"Iron Overload, Autosomal Dominant",,,,,,,C1851316,C565020,615517,MONDO:0014225,hemochromatosis type 5,
+BMGC_DS11161,BMG_DS039434,,"Familial Mediterranean Fever, Autosomal Dominant",Familial Mediterranean Fever,,,,,,C1851347,D010505,134610,MONDO:0007601,"familial Mediterranean fever, autosomal dominant",
+BMGC_DS11162,BMG_DS039435,,Familial Multiple Coagulation Factor Deficiency VI,,,,,,,C1851374,C565022,134540,MONDO:0007599,"factor 9 and Factor XI, combined deficiency of",
+BMGC_DS11163,BMG_DS039437,,Familial Multiple Coagulation Factor Deficiency II,,,,,,,C1851376,C565024,134510,MONDO:0007597,"factor VIII and Factor IX, combined deficiency of",
+BMGC_DS11164,BMG_DS039438,,Familial Multiple Coagulation Factor Deficiency IV,,,,,,,C1851377,C565025,134430,MONDO:0007595,"factor VII and Factor VIII, combined deficiency of",
+BMGC_DS11165,BMG_DS039439,,Factor V Excess with Spontaneous Thrombosis,,,,,,,C1851378,C565026,134400,MONDO:0007594,factor 5 excess with spontaneous thrombosis,
+BMGC_DS11166,BMG_DS039440,,"Facial Palsy, Familial Recurrent Peripheral",,,,,,,C1851399,C565028,134200,MONDO:0007592,familial recurrent peripheral facial palsy,
+BMGC_DS11167,BMG_DS039441,,Exudative vitreoretinopathy 1,,,,,DOID:0111412,exudative vitreoretinopathy 1,C1851402,C536382,133780,MONDO:0007589,exudative vitreoretinopathy 1,
+BMGC_DS11168,BMG_DS039443,,"EXOSTOSES, MULTIPLE, TYPE II",,,,,,,C1851413,,133701;608210,MONDO:0007586,"exostoses, multiple, type 2",
+BMGC_DS11169,BMG_DS039444,,"Exostoses with Anetodermia and Brachydactyly, Type E",,,,,,,C1851428,C565034,133690,MONDO:0007584,exostoses-anetodermia-brachydactyly type E syndrome,
+BMGC_DS11170,BMG_DS039445,,Cerebrooculofacioskeletal Syndrome 3,,,,,DOID:0080913,cerebrooculofacioskeletal syndrome 3,C1851443,C565035,616570,MONDO:0014696,cerebrooculofacioskeletal syndrome 3,
+BMGC_DS11171,BMG_DS039446,,"Exchondrosis Of Pinna, Posterior",,,,,,,C1851463,C565036,133500,MONDO:0007581,"exchondrosis of pinna, posterior",
+BMGC_DS11172,BMG_DS039448,,Greither Disease,Erythrokeratodermia Variabilis,,,,DOID:0050467,erythrokeratodermia variabilis,C1851480,D056266,,MONDO:0018853,transgrediens et progrediens palmoplantar keratoderma,
+BMGC_DS11173,BMG_DS039449,719255000,Erythrokeratodermia with ataxia,,,,,,,C1851481,C535738,133190,MONDO:0007574,spinocerebellar ataxia type 34,Spinocerebellar ataxia type 34 (disorder) | Spinocerebellar ataxia type 34 | Erythrokeratodermia with ataxia | Spinocerebellar ataxia and erythrokeratodermia
+BMGC_DS11174,BMG_DS039450,,Erythema Palmare Hereditarium,,,,,,,C1851502,C565041,133000,MONDO:0007570,erythema palmare hereditarium,
+BMGC_DS11175,BMG_DS039451,,"Erythema nodosum, familial",,,,,,,C1851503,C535510,132990,MONDO:0007569,"erythema nodosum, familial",
+BMGC_DS11176,BMG_DS039452,,"Aortic aneurysm, familial thoracic 4",,,,,,,C1851504,C537784,132900,MONDO:0007568,"aortic aneurysm, familial thoracic 4",
+BMGC_DS11177,BMG_DS039455,,,,,,,,,C1851526,,132700,MONDO:0007565,familial cylindromatosis,
+BMGC_DS11178,BMG_DS039456,,"Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness",,,,,DOID:0111348,multiple epiphyseal dysplasia with myopia and deafness,C1851536,C565046,132450,MONDO:0007562,"multiple epiphyseal dysplasia, Beighton type",
+BMGC_DS11179,BMG_DS039459,,Benign Occipital Epilepsy,"Epilepsies, Partial",,,,,,C1851549,D004828,132090,MONDO:0007558,self-limited childhood occipital epilepsy,
+BMGC_DS11180,BMG_DS039460,,Epidermolysis Bullosa with Deficiency of Galactosylhydroxylysyl Glucosyltransferase,,,,,,,C1851570,C565049,131880,MONDO:0007553,epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase,
+BMGC_DS11181,BMG_DS039461,,Transient bullous dermolysis of the newborn,,,,,DOID:0111345,transient bullous dermolysis of the newborn,C1851573,C536979,131705,MONDO:0007548,transient bullous dermolysis of the newborn,
+BMGC_DS11182,BMG_DS039464,,"MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA",,,,,DOID:0111344,myeloproliferative disorder with eosinophilia,C1851585,,131440,MONDO:0007546,"myeloproliferative disorder, chronic, with eosinophilia",
+BMGC_DS11183,BMG_DS039465,,EOSINOPHILOPENIA,,,,,,,C1851586,,131430,MONDO:0007545,Eosinophilopenia,
+BMGC_DS11184,BMG_DS039466,,,,,,,,,C1851649,,131200,MONDO:0007541,"endometriosis, susceptibility to, 1",
+BMGC_DS11185,BMG_DS039468,,LATERAL MENINGOCELE SYNDROME,,,,,DOID:0111343,lateral meningocele syndrome,C1851710,,600276;130720,MONDO:0007537,lateral meningocele syndrome,
+BMGC_DS11186,BMG_DS039469,,"Emphysema, Hereditary Pulmonary",,,,,,,C1851718,C565057,130700,MONDO:0007535,"emphysema, hereditary pulmonary",
+BMGC_DS11187,BMG_DS039470,,Elliptocytosis 2,,,,,,,C1851741,C565058,130600,MONDO:0007533,elliptocytosis 2,
+BMGC_DS11188,BMG_DS039471,,,,,,,,,C1851756,,130300,MONDO:0007531,electroencephalographic peculiarity: fronto-precentral beta wave groups,
+BMGC_DS11189,BMG_DS039472,,,,,,,,,C1851757,,130200,MONDO:0007530,electroencephalographic peculiarity: 14 and 6 per sec. positive spike phenomenon,
+BMGC_DS11190,BMG_DS039473,,EDS VIIB,,,,,DOID:0080728,Ehlers-Danlos syndrome arthrochalasia type 2,C1851801,C565061,617821,MONDO:0020522,Ehlers-Danlos syndrome type 7B,
+BMGC_DS11191,BMG_DS039474,,"ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1",,,,,,,C1851841,,129900,MONDO:0007520,"ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1",
+BMGC_DS11192,BMG_DS039475,,"Edema, Familial Idiopathic, Prepubertal",,,,,,,C1851847,C565063,129840,MONDO:0007518,"edema, familial idiopathic, prepubertal",
+BMGC_DS11193,BMG_DS039477,,Ectrodactyly and Ectodermal Dysplasia without Cleft Lip-Palate,,,,,,,C1851849,C565065,129810,MONDO:0007516,ectrodactyly and ectodermal dysplasia without cleft lip/palate,
+BMGC_DS11194,BMG_DS039478,,Ectodermal dysplasia adrenal cyst,,,,,,,C1851850,C538015,129550,MONDO:0007513,ectodermal dysplasia with adrenal cyst,
+BMGC_DS11195,BMG_DS039481,,OROFACIAL CLEFT 8,,,,,DOID:0080401,orofacial cleft 8,C1851878,,603273;618149,MONDO:0029145,orofacial cleft 8,
+BMGC_DS11196,BMG_DS039482,,ECHO VIRUS 11 SENSITIVITY,,,,,,,C1851888,,129150,,,
+BMGC_DS11197,BMG_DS039483,,,,,,,,,C1851895,,129000,MONDO:0007505,"earring holes, natural",
+BMGC_DS11198,BMG_DS039484,,,,,,,,,C1851896,,128980,MONDO:0007504,thickened earlobes-conductive deafness syndrome,
+BMGC_DS11199,BMG_DS039485,,,,,,,,,C1851899,,128800,MONDO:0007503,ear without helix,
+BMGC_DS11200,BMG_DS039486,,,,,,,,,C1851900,,128710,MONDO:0007502,"ear pits, posterior helical",
+BMGC_DS11201,BMG_DS039487,,,,,,,,,C1851901,,128500,MONDO:0007499,ear folding,
+BMGC_DS11202,BMG_DS039488,,,,,,,,,C1851905,,128290,MONDO:0007497,"ear antitragus, tag at base of",
+BMGC_DS11203,BMG_DS039489,,Dopa-Responsive Dystonia,,,,,,,C1851920,C538007,128230,MONDO:0016812;MONDO:0007495,dopa-responsive dystonia | dystonia 5,
+BMGC_DS11204,BMG_DS039491,49949003,Paroxysmal choreoathetosis,,,,,,,C1851936,,,,,Paroxysmal choreoathetosis | Paroxysmal choreoathetosis (disorder) | Paroxysmal dyskinesia
+BMGC_DS11205,BMG_DS039492,,Dystonia musculorum deformans 4,,,,,,,C1851943,C538004,128101,MONDO:0007493,torsion dystonia 4,
+BMGC_DS11206,BMG_DS039493,,"DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT",,,,,,,C1851945,,128100;605204,MONDO:0007492,early-onset generalized limb-onset dystonia,
+BMGC_DS11207,BMG_DS039494,,Dystelephalangy,,,,,,,C1851955,C538000,128000,MONDO:0007491,dystelephalangy,
+BMGC_DS11208,BMG_DS039498,,,,,,,,,C1851967,,127700,MONDO:0007487,"dyslexia, susceptibility to, 1",
+BMGC_DS11209,BMG_DS039502,,"Dwarfism, Levi Type",,,,,,,C1851994,C565081,127100,MONDO:0007479,"dwarfism, Levi type",
+BMGC_DS11210,BMG_DS039503,,Dwarfism tall vertebrae,,,,,,,C1851996,C535725,126950,MONDO:0020792,dwarfism with tall vertebrae,
+BMGC_DS11211,BMG_DS039506,,"Duodenal Ulcer, Hyperpepsinogenemic I",,,,,,,C1852008,C565086,126850,MONDO:0007475,"duodenal ulcer, hyperpepsinogenemic 1",
+BMGC_DS11212,BMG_DS039507,,Duodenal ulcer due to antral G-cell hyperfunction,,,,,,,C1852009,C535721,126840,MONDO:0007474,duodenal ulcer due to antral G-cell hyperfunction,
+BMGC_DS11213,BMG_DS039508,720598005,Doughnut lesion of calvaria and bone fragility syndrome,,,,,,,C1852022,,126550,MONDO:0007470,calvarial doughnut lesions-bone fragility syndrome,Doughnut lesion of calvaria and bone fragility syndrome (disorder) | Doughnut lesion of calvaria and bone fragility syndrome | Calvarial doughnut lesion with bone fragility syndrome | Familial doughnut lesions of skull
+BMGC_DS11214,BMG_DS039509,,,,,,,,,C1852023,,126500,MONDO:0007469,double nail for fifth toe,
+BMGC_DS11215,BMG_DS039511,,Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature,,,,,,,C1852062,C565092,126320,MONDO:0007465,distichiasis with congenital anomalies of the heart and peripheral vasculature,
+BMGC_DS11216,BMG_DS039514,,,,,,,,,C1852074,,126180,MONDO:0007460,"discrimination, Two-point, reduction 1N",
+BMGC_DS11217,BMG_DS039515,,Digitotalar Dysmorphism,,,,,DOID:0111596,distal arthrogryposis type 1,C1852085,C565097,126050,MONDO:0007458;MONDO:0015240,"digitotalar dysmorphism; ulnar drift, hereditary | digitotalar dysmorphism",
+BMGC_DS11218,BMG_DS039516,,,,,,,,,C1852086,,125900,MONDO:0007457,"diastema, dental medial",
+BMGC_DS11219,BMG_DS039518,,"DIABETES MELLITUS, INSULIN-DEPENDENT, 2",,,,,,,C1852092,,125852,MONDO:0007454,type 1 diabetes mellitus 2,
+BMGC_DS11220,BMG_DS039519,,"Maturity-Onset Diabetes of the Young, Type 1",,,,,,,C1852093,C565101,125850,MONDO:0007452,maturity-onset diabetes of the young type 1,
+BMGC_DS11221,BMG_DS039520,,KERATOSIS PALMOPLANTARIS STRIATA II,,,,,,,C1852127,,125647;612908,MONDO:0013034,keratosis palmoplantaris striata 2,
+BMGC_DS11222,BMG_DS039521,,Dermoodontodysplasia,,,,,,,C1852144,C565103,125640,MONDO:0007449,dermo-odonto dysplasia,
+BMGC_DS11223,BMG_DS039522,,Familial dermographism,,,,,,,C1852145,C536612,125635,MONDO:0007448,familial dermatographia,
+BMGC_DS11224,BMG_DS039523,,DERMODISTORTIVE URTICARIA,,,,,,,C1852146,,125630,,,
+BMGC_DS11225,BMG_DS039524,,,,,,,,,C1852150,,136000,MONDO:0007619,isolated congenital adermatoglyphia,
+BMGC_DS11226,BMG_DS039527,,"Dermal Ridges, Patternless",,,,,,,C1852160,C565109,125540,MONDO:0007444,"dermal Ridges, patternless",
+BMGC_DS11227,BMG_DS039529,,,,,,,,,C1852197,,125480,MONDO:0007440,major affective disorder 1,
+BMGC_DS11228,BMG_DS039530,,Deoxyribose-5-Phosphate Aldolase Deficiency,,,,,,,C1852200,C565112,125460,MONDO:0007439,deoxyribose-5-phosphate aldolase deficiency,
+BMGC_DS11229,BMG_DS039531,,Dentin dysplasia sclerotic bones,,,,,,,C1852201,C538213,125440,MONDO:0007438,dentin dysplasia-sclerotic bones syndrome,
+BMGC_DS11230,BMG_DS039532,,"Failure of Tooth Eruption, Primary",,,,,DOID:0111341,primary failure of tooth eruption,C1852222,C565114,125350,MONDO:0007434,primary failure of tooth eruption,
+BMGC_DS11231,BMG_DS039533,,Dementia-Parkinsonism With Non-Alzheimer Amyloid Plaques,,,,,,,C1852223,C565115,125320,MONDO:0007433,dementia/parkinsonism with non-Alzheimer amyloid plaques,
+BMGC_DS11232,BMG_DS039537,,Auditory neuropathy,,,,,,,C1852271,C538268,MTHU018711,MONDO:0021944,auditory neuropathy,
+BMGC_DS11233,BMG_DS039539,,Deafness with Anhidrotic Ectodermal Dysplasia,,,,,,,C1852279,C565119,125050,MONDO:0007427,deafness with anhidrotic ectodermal dysplasia,
+BMGC_DS11234,BMG_DS039540,,"Deafness, Sensorineural, with Peripheral Neuropathy and Arterial Disease",,,,,,,C1852280,C565120,124950,MONDO:0007425,"deafness, sensorineural, with peripheral neuropathy and arterial disease",
+BMGC_DS11235,BMG_DS039541,,"Deafness, Autosomal Dominant 1",,,,,,,C1852282,C565121,124900,MONDO:0007424,autosomal dominant nonsyndromic hearing loss 1,
+BMGC_DS11236,BMG_DS039542,,"Deafness, Mid-Tone Neural",,,,,,,C1852283,C565122,124700,MONDO:0007423,"deafness, mid-tone neural",
+BMGC_DS11237,BMG_DS039544,,,,,,,,,C1852294,,124300;124400,MONDO:0007418,Darwinian tubercle of pinna,
+BMGC_DS11238,BMG_DS039545,,"Darier Disease, Acral Hemorrhagic Type",,,,,,,C1852296,C565125,,,,
+BMGC_DS11239,BMG_DS039546,,"Darier Disease, Segmental",,,,,,,C1852297,C565126,,,,
+BMGC_DS11240,BMG_DS039548,,Mitochondrial Complex III Deficiency,,,,,DOID:0111139,mitochondrial complex III deficiency,C1852372,C565128,,MONDO:0015448,mitochondrial complex III deficiency,
+BMGC_DS11241,BMG_DS039549,,Mitochondrial encephalopathy,,,,,,,C1852373,C538525,MTHU018751,,,
+BMGC_DS11242,BMG_DS039552,,Cutis Gyrata Syndrome of Beare And Stevenson,,,,,,,C1852406,C565129,123790,MONDO:0007412,Beare-Stevenson cutis gyrata syndrome,
+BMGC_DS11243,BMG_DS039555,,"CATARACT, COPPOCK-LIKE",,,,,,,C1852438,,604307,,,
+BMGC_DS11244,BMG_DS039558,,"Cryptophthalmos, Unilateral or Bilateral, Isolated",,,,,DOID:0111717,isolated cryptophthalmia,C1852453,C565138,123570,MONDO:0007410,isolated cryptophthalmia,
+BMGC_DS11245,BMG_DS039560,,"Cryptotia, Familial",,,,,,,C1852455,C565140,123557,MONDO:0007408,"cryptotia, familial",
+BMGC_DS11246,BMG_DS039561,,"Cryoglobulinemia, Familial Mixed",,,,,,,C1852456,C565141,123550,MONDO:0007407,Cryoglobulinemic vasculitis,
+BMGC_DS11247,BMG_DS039562,,"Cryofibrinogenemia, Familial Primary",,,,,,,C1852457,C565142,123540,MONDO:0007406,"cryofibrinogenemia, familial primary",
+BMGC_DS11248,BMG_DS039566,,"CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT",,,,,DOID:0080801,autosomal dominant craniometaphyseal dysplasia,C1852502,,123000;605145,MONDO:0007397,"craniometaphyseal dysplasia, autosomal dominant",
+BMGC_DS11249,BMG_DS039567,702362004,Craniofacial deafness hand syndrome,,,,,DOID:0111336,craniofacial-deafness-hand syndrome,C1852510,C536453,122880,MONDO:0007395,craniofacial-deafness-hand syndrome,Craniofacial deafness hand syndrome (disorder) | Craniofacial deafness hand syndrome | Sommer Young Wee Frye syndrome
+BMGC_DS11250,BMG_DS039568,,Cranioacrofacial Syndrome,,,,,,,C1852512,C565147,122850,MONDO:0007393,cranioacrofacial syndrome,
+BMGC_DS11251,BMG_DS039569,,Coxoauricular Syndrome,,,,,,,C1852513,C565148,122780,MONDO:0007392,coxoauricular syndrome,
+BMGC_DS11252,BMG_DS039572,,,,,,,,,C1852523,,122580,MONDO:0007388,congenitally short costocoracoid ligament,
+BMGC_DS11253,BMG_DS039573,,Corticosteroid-Binding Globulin Deficiency,,,,,DOID:0090030,corticosteroid-binding globulin deficiency,C1852529,C565152,611489,MONDO:0012675,corticosteroid-binding globulin deficiency,
+BMGC_DS11254,BMG_DS039574,,"Coronary Artery Dissection, Spontaneous",,,,,,,C1852540,C565153,122455,MONDO:0007385,idiopathic spontaneous coronary artery dissection,
+BMGC_DS11255,BMG_DS039577,,Epithelial Recurrent Erosion Dystrophy,,,,,DOID:0070337,epithelial recurrent erosion dystrophy,C1852551,C565155,122400,MONDO:0007381,epithelial recurrent erosion dystrophy,
+BMGC_DS11256,BMG_DS039578,,"Corneal Dystrophy, Posterior Polymorphous, 1",,,,,DOID:0060457,posterior polymorphous corneal dystrophy,C1852555,C562745,122000,MONDO:0007378,posterior polymorphous corneal dystrophy 1,
+BMGC_DS11257,BMG_DS039580,,,,,,,,,C1852557,,121400,MONDO:0007372,"cornea plana 1, autosomal dominant",
+BMGC_DS11258,BMG_DS039581,,Cornea guttata with anterior polar cataract,,,,,,,C1852558,C535471,121390,MONDO:0007371,cornea guttata with anterior polar cataracts,
+BMGC_DS11259,BMG_DS039582,,,,,,,,,C1852561,,121350,MONDO:0007370,"coracoclavicular joint, anomalous",
+BMGC_DS11260,BMG_DS039583,,"Copper deficiency, familial benign",,,,,,,C1852576,C535468,121270,MONDO:0007368,familial benign copper deficiency,
+BMGC_DS11261,BMG_DS039584,,"Febrile Convulsions, Familial, 1",,,,,,,C1852577,C565162,121210,MONDO:0007367,"febrile seizures, familial, 1",
+BMGC_DS11262,BMG_DS039585,,,,,,,,,C1852581,,121201,MONDO:0007366,"seizures, benign familial neonatal, 2",
+BMGC_DS11263,BMG_DS039588,,"Arthrogryposis, distal, type 2E",,,,,,,C1852597,C535384,121070,MONDO:0007364,"arthrogryposis, distal, type 2E",
+BMGC_DS11264,BMG_DS039589,,"Complement Component 4, Partial Deficiency Of",,,,,,,C1852700,C565168,120790,MONDO:0007361,C1 inhibitor deficiency,
+BMGC_DS11265,BMG_DS039590,,Branchiootic Syndrome 2,,,,,,,C1852718,C565171,120502,MONDO:0007360,branchiootic syndrome 2,
+BMGC_DS11266,BMG_DS039593,,COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY,,,,,,,C1852752,,120400,MONDO:0007353,coloboma of macula-brachydactyly type B syndrome,
+BMGC_DS11267,BMG_DS039594,446449009,Papillorenal syndrome,,,,,,,C1852759,C537168,120330,MONDO:0007352,renal coloboma syndrome,Renal coloboma syndrome (disorder) | Papillorenal syndrome | Renal coloboma syndrome
+BMGC_DS11268,BMG_DS039595,,,,,,,,,C1852767,,120300,MONDO:0007351,coloboma of macula,
+BMGC_DS11269,BMG_DS039596,,"CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2",,,,,,,C1852795,,609140,MONDO:0012199,posterior polymorphous corneal dystrophy 2,
+BMGC_DS11270,BMG_DS039598,,Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia,,,,,,,C1852989,C565179,619248,MONDO:0031001,vitreoretinopathy with phalangeal epiphyseal dysplasia,
+BMGC_DS11271,BMG_DS039599,,Cornelia de Lange Syndrome 3,De Lange Syndrome,,,,,,C1853099,D003635,610759,MONDO:0012555,Cornelia de Lange syndrome 3,
+BMGC_DS11272,BMG_DS039600,,CEREBROOCULOFACIOSKELETAL SYNDROME 4,,,,,,,C1853100,,610758;126380,MONDO:0012554,cerebrooculofacioskeletal syndrome 4,
+BMGC_DS11273,BMG_DS039601,,Cerebrooculofacioskeletal Syndrome 2,,,,,DOID:0080912,cerebrooculofacioskeletal syndrome 2,C1853102,C565185,610756,MONDO:0012553,cerebrooculofacioskeletal syndrome 2,
+BMGC_DS11274,BMG_DS039602,,ALOPECIA AREATA 2,,,,,,,C1853104,,610753,MONDO:0012551,alopecia areata 2,
+BMGC_DS11275,BMG_DS039604,,"Spinocerebellar Ataxia, Autosomal Recessive 8",,,,,DOID:0111618,autosomal recessive spinocerebellar ataxia 8,C1853116,C565188,610743,MONDO:0012549,"autosomal recessive ataxia, Beauce type",
+BMGC_DS11276,BMG_DS039605,89655007,Severe congenital neutropenia,,,,,,,C1853118,,MTHU008417,MONDO:0018542,severe congenital neutropenia,Congenital neutropenia | Severe infantile genetic neutropenia | Primary neutropenia | Severe congenital neutropenia | Congenital neutropenia (disorder)
+BMGC_DS11277,BMG_DS039606,,Noonan Syndrome 4,,,,,DOID:0060582,Noonan syndrome 4,C1853120,C548082,610733,MONDO:0012547,Noonan syndrome 4,
+BMGC_DS11278,BMG_DS039607,,"NEPHROTIC SYNDROME, TYPE 3",,,,,DOID:0080382,nephrotic syndrome type 3,C1853124,,610725;608414,MONDO:0012546,"nephrotic syndrome, type 3",
+BMGC_DS11279,BMG_DS039608,,Neutral Lipid Storage Disease with Myopathy,,,,,,,C1853136,C565192,610717,MONDO:0012545,neutral lipid storage myopathy,
+BMGC_DS11280,BMG_DS039609,,BRACHYDACTYLY-SYNDACTYLY SYNDROME,,,,,,,C1853137,,610713;142989,MONDO:0012544,brachydactyly-syndactyly syndrome,
+BMGC_DS11281,BMG_DS039610,,Optic atrophy 5,,,,,DOID:0111438,optic atrophy 5,C1853139,C537126,610708,MONDO:0012543,optic atrophy 5,
+BMGC_DS11282,BMG_DS039612,,"Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia",,,,,,,C1853144,C565195,610706,MONDO:0012541,"deafness with labyrinthine aplasia, microtia, and microdontia",
+BMGC_DS11283,BMG_DS039613,,"Macular Degeneration, Age-Related, 4",,,,,,,C1853147,C565196,610698,MONDO:0012540,age related macular degeneration 4,
+BMGC_DS11284,BMG_DS039614,,JOUBERT SYNDROME 6,,,,,,,C1853153,,610688;609884,MONDO:0012539,Joubert syndrome 6,
+BMGC_DS11285,BMG_DS039615,,Nemaline Myopathy 7,,,,,DOID:0110934,nemaline myopathy 7,C1853154,C565198,610687,MONDO:0012538,nemaline myopathy 7,
+BMGC_DS11286,BMG_DS039617,,Osteogenesis Imperfecta Type VII,,,,,DOID:0110337,osteogenesis imperfecta type 7,C1853162,C565200,610682,MONDO:0012536,osteogenesis imperfecta type 7,
+BMGC_DS11287,BMG_DS039620,,Recurrent skin infections,,,,,,,C1853193,,MTHU000084,,,
+BMGC_DS11288,BMG_DS039624,,,,,,,,,C1853198,,610313,MONDO:0012467,cold-induced sweating syndrome 2,
+BMGC_DS11289,BMG_DS039625,,,,,,,,,C1853202,,610297,MONDO:0012466,"Parkinson disease 13, autosomal dominant, susceptibility to",
+BMGC_DS11290,BMG_DS039627,,RETINITIS PIGMENTOSA 35,,,,,,,C1853214,,610282;607292,MONDO:0012463,retinitis pigmentosa 35,
+BMGC_DS11291,BMG_DS039628,,"Pachygyria, frontotemporal",,,,,,,C1853215,C538092,610279,MONDO:0012462,autosomal recessive frontotemporal pachygyria,
+BMGC_DS11292,BMG_DS039629,,"Deafness, Autosomal Recessive 67",,,,,,,C1853223,C565207,610265,MONDO:0012460,autosomal recessive nonsyndromic hearing loss 67,
+BMGC_DS11293,BMG_DS039633,,,,,,,,,C1853230,,610256,MONDO:0012456,congenital primary aphakia,
+BMGC_DS11294,BMG_DS039634,,Sclerocornea,,,,,DOID:0060252,sclerocornea,C1853235,C565209,MTHU000241,MONDO:0019629,sclerocornea,
+BMGC_DS11295,BMG_DS039635,,"SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT",,,,,,,C1853247,,609139;610250,MONDO:0012453,hereditary spastic paraplegia 31,
+BMGC_DS11296,BMG_DS039636,,"DEAFNESS, AUTOSOMAL RECESSIVE 65",,,,,,,C1853248,,610248,MONDO:0012452,autosomal recessive nonsyndromic hearing loss 65,
+BMGC_DS11297,BMG_DS039637,,SPINOCEREBELLAR ATAXIA 28,,,,,DOID:0050977,spinocerebellar ataxia type 28,C1853249,,610246;604581,MONDO:0012450,spinocerebellar ataxia type 28,
+BMGC_DS11298,BMG_DS039638,,SPINOCEREBELLAR ATAXIA 23,,,,,DOID:0050973,spinocerebellar ataxia type 23,C1853250,,131340;610245,MONDO:0012449,spinocerebellar ataxia type 23,
+BMGC_DS11299,BMG_DS039639,,"Spastic Paraplegia 33, Autosomal Dominant",,,,,,,C1853251,C565214,610244,MONDO:0012448,hereditary spastic paraplegia 33,
+BMGC_DS11300,BMG_DS039642,,Seborrhea-Like Dermatitis with Psoriasiform Elements,,,,,,,C1853258,C565217,610227,MONDO:0012446,seborrhea-like dermatitis with psoriasiform elements,
+BMGC_DS11301,BMG_DS039643,,"HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY",,,,,DOID:0050947,hereditary hypophosphatemic rickets with hypercalciuria,C1853271,,241530;609826,MONDO:0009431,hereditary hypophosphatemic rickets with hypercalciuria,
+BMGC_DS11302,BMG_DS039644,,"Deafness, Autosomal Recessive 28",,,,,,,C1853276,C565218,609823,MONDO:0012355,autosomal recessive nonsyndromic hearing loss 28,
+BMGC_DS11303,BMG_DS039645,,Bleeding Disorder Due To P2RY12 Defect,,,,,,,C1853278,C565220,609821,MONDO:0012354,platelet-type bleeding disorder 8,
+BMGC_DS11304,BMG_DS039646,,"Erythrocytosis, Familial, 3",,,,,,,C1853286,C565221,609820,MONDO:0012353,"erythrocytosis, familial, 3",
+BMGC_DS11305,BMG_DS039648,,Zygodactyly 1,,,,,DOID:0111820,zygodactyly 1,C1853294,C565223,609815,MONDO:0012351,zygodactyly type 1,
+BMGC_DS11306,BMG_DS039649,,"Spondylocostal Dysostosis 3, Autosomal Recessive",,,,,,,C1853296,C535781,609813,MONDO:0010180;MONDO:0012349,"autosomal recessive spondylocostal dysostosis | spondylocostal dysostosis 3, autosomal recessive",
+BMGC_DS11307,BMG_DS039650,,"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 8, WITH EXOCRINE DYSFUNCTION",,,,,DOID:0111105,maturity-onset diabetes of the young type 8,C1853297,,609812;114840,MONDO:0012348,maturity-onset diabetes of the young type 8,
+BMGC_DS11308,BMG_DS039651,,"Hamartoma, Precalcaneal Congenital Fibrolipomatous",,,,,,,C1853298,C565226,609808,MONDO:0012347,"hamartoma, Precalcaneal congenital fibrolipomatous",
+BMGC_DS11309,BMG_DS039652,,"Generalized Epilepsy With Febrile Seizures Plus, Type 4",,,,,,,C1853345,C565227,609800,MONDO:0012346,"generalized epilepsy with febrile seizures plus, type 4",
+BMGC_DS11310,BMG_DS039653,709416009,"Peeling skin syndrome, acral type",,,,,DOID:0070521,peeling skin syndrome 2,C1853354,C536316,609796,MONDO:0012345,acral peeling skin syndrome,"Peeling skin syndrome, acral type | Acral peeling skin syndrome | Acral peeling skin syndrome (disorder)"
+BMGC_DS11311,BMG_DS039656,,,,,,,,,C1853365,,100070,MONDO:0024521,"aortic aneurysm, familial abdominal, 1",
+BMGC_DS11312,BMG_DS039657,,,,,,,,,C1853371,,606394,MONDO:0011668,maturity-onset diabetes of the young type 6,
+BMGC_DS11313,BMG_DS039658,,,,,,,,,C1853377,,,MONDO:0019953,mega-cisterna magna,
+BMGC_DS11314,BMG_DS039659,,"Interleukin 2 Receptor, Alpha, Deficiency of",,,,,DOID:0111968,immunodeficiency 41,C1853392,C565232,606367,MONDO:0011664,immunodeficiency due to CD25 deficiency,
+BMGC_DS11315,BMG_DS039660,,Primary lateral sclerosis juvenile,,,,,,,C1853396,C536416,606353,MONDO:0011663,juvenile primary lateral sclerosis,
+BMGC_DS11316,BMG_DS039661,,INFLAMMATORY BOWEL DISEASE 5,,,,,,,C1853438,,606348,MONDO:0011661,inflammatory bowel disease 5,
+BMGC_DS11317,BMG_DS039662,,"Heterotaxy, Visceral, 3, Autosomal",,,,,,,C1853444,C565237,606325,MONDO:0011659,"heterotaxy, visceral, 3, autosomal",
+BMGC_DS11318,BMG_DS039663,,"PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET",,,,,DOID:0060370,Parkinson's disease 7,C1853445,,602533;606324,MONDO:0011658,autosomal recessive early-onset Parkinson disease 7,
+BMGC_DS11319,BMG_DS039664,,"Deafness, Autosomal Dominant 24",,,,,,,C1853451,C565239,606282,MONDO:0011657,autosomal dominant nonsyndromic hearing loss 24,
+BMGC_DS11320,BMG_DS039665,,PAGET DISEASE OF BONE 4,,,,,DOID:0081367,Paget's disease of bone 4,C1853473,,606263,MONDO:0011656,paget disease of bone 4,
+BMGC_DS11321,BMG_DS039666,,"Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism",,,,,,,C1853480,C565246,606242,MONDO:0011654,"intellectual disability, microcephaly, growth retardation, joint contractures, and facial dysmorphism",
+BMGC_DS11322,BMG_DS039667,,22q13.3 Deletion Syndrome,,,,,,,C1853490,C536801,606232,MONDO:0011652,Phelan-McDermid syndrome,
+BMGC_DS11323,BMG_DS039668,,"Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations",,,,,,,C1853507,C565248,606220,MONDO:0011651,"intellectual disability, short stature, facial anomalies, and joint dislocations",
+BMGC_DS11324,BMG_DS039669,,,,,,,,,C1853508,,606217,MONDO:0011650,"atrioventricular septal defect, susceptibility to, 2",
+BMGC_DS11325,BMG_DS039670,,"Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome",,,,,,,C1853509,C565249,,,,
+BMGC_DS11326,BMG_DS039677,,Genitopatellar Syndrome,,,,,,,C1853566,C565255,606170,MONDO:0011640,genitopatellar syndrome,
+BMGC_DS11327,BMG_DS039680,699299001,Neuroferritinopathy,,,,,DOID:0110737,neurodegeneration with brain iron accumulation 3,C1853578,C548080,606159,MONDO:0011638,neuroferritinopathy,Adult onset basal ganglia disease | Neuroferritinopathy (disorder) | Ferritin related neurodegeneration | Neuroferritinopathy
+BMGC_DS11328,BMG_DS039682,,Fryns-Aftimos Syndrome,,,,,,,C1853623,C565258,,MONDO:0017579,Baraitser-Winter cerebrofrontofacial syndrome,
+BMGC_DS11329,BMG_DS039683,,"Anemia, Diamond-Blackfan, 2",,,,,DOID:0111885,Diamond-Blackfan anemia 2,C1853666,C536130,606129,MONDO:0011636,Diamond-Blackfan anemia 2,
+BMGC_DS11330,BMG_DS039684,,"Goiter, Multinodular 3",,,,,,,C1853686,C565260,606082,MONDO:0011635,"goiter, multinodular 3",
+BMGC_DS11331,BMG_DS039685,709281006,Rippling muscle disease,,,,,DOID:0070308;DOID:0060255,rippling muscle disease 1 | rippling muscle disease 2,C1853698,C535686,,MONDO:0011634,rippling muscle disease,Rippling muscle disease (disorder) | Rippling muscle disease | Rippling muscle syndrome
+BMGC_DS11332,BMG_DS039686,,"Hereditary Motor And Sensory Neuropathy, Type IIC",,,,,,,C1853710,C565261,606071,MONDO:0011633,Charcot-Marie-Tooth disease axonal type 2C,
+BMGC_DS11333,BMG_DS039687,,,,,,,,,C1853723,,,MONDO:0018951,distal myopathy with vocal cord weakness,
+BMGC_DS11334,BMG_DS039688,,"HEMOCHROMATOSIS, TYPE 4",,,,,DOID:0111028,hemochromatosis type 4,C1853733,,604653;606069,MONDO:0011631,hemochromatosis type 4,
+BMGC_DS11335,BMG_DS039689,,"Congenital Disorder Of Glycosylation, Type IIB",,,,,DOID:0070254,congenital disorder of glycosylation type IIb,C1853736,C565264,606056,MONDO:0011629,MOGS-congenital disorder of glycosylation,
+BMGC_DS11336,BMG_DS039690,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY,,,,,,,C1853755,,604616;606053,MONDO:0011627,"autism, susceptibility to, 5",
+BMGC_DS11337,BMG_DS039692,,"Deafness, Autosomal Dominant 18",,,,,,,C1853760,C565267,606012,MONDO:0011625,autosomal dominant nonsyndromic hearing loss 18,
+BMGC_DS11338,BMG_DS039693,,,,,,,,,C1853761,,606002,MONDO:0018996,"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2",
+BMGC_DS11339,BMG_DS039695,,Familial Wilms tumor 2,,,,,,,C1853800,C536853,,,,
+BMGC_DS11340,BMG_DS039696,720412009,Acropectoral syndrome,,,,,,,C1853812,C535664,605967,MONDO:0011621,acropectoral syndrome,Acropectoral syndrome (disorder) | Acropectoral syndrome | Acro-pectoral syndrome | Syndactyly with preaxial polydactyly and sternal deformity syndrome
+BMGC_DS11341,BMG_DS039701,,Holoprosencephaly 6,,,,,DOID:0110874,holoprosencephaly 6,C1853830,C565274,605934,MONDO:0011616,holoprosencephaly 6,
+BMGC_DS11342,BMG_DS039703,,"Parkinson Disease 6, Autosomal Recessive Early-Onset",,,,,,,C1853833,C565276,605909,MONDO:0011613,autosomal recessive early-onset Parkinson disease 6,
+BMGC_DS11343,BMG_DS039704,,"Cardiomyopathy, Dilated, with Left Ventricular Noncompaction",,,,,,,C1853863,C565277,,,,
+BMGC_DS11344,BMG_DS039705,,Dimethylglycine Dehydrogenase Deficiency,,,,,,,C1853892,C565278,605850,MONDO:0011610,dimethylglycine dehydrogenase deficiency,
+BMGC_DS11345,BMG_DS039710,,"Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant",,,,,,,C1853919,C565284,605827,MONDO:0011605,generalized basaloid follicular hamartoma syndrome,
+BMGC_DS11346,BMG_DS039711,,"Spondyloocular Syndrome, Autosomal Recessive",,,,,,,C1853925,C565285,,,,
+BMGC_DS11347,BMG_DS039712,,NONAKA MYOPATHY,,,,,DOID:0080718,GNE myopathy,C1853926,,603824;605820,MONDO:0011603,GNE myopathy,
+BMGC_DS11348,BMG_DS039713,,"DEAFNESS, AUTOSOMAL RECESSIVE 27",,,,,,,C1853941,,605818,MONDO:0011602,autosomal recessive nonsyndromic hearing loss 27,
+BMGC_DS11349,BMG_DS039714,,"CITRULLINEMIA, TYPE II, NEONATAL-ONSET",,,,,DOID:0070341,neonatal-onset type II citrullinemia,C1853942,,605814;603859,MONDO:0011601,neonatal intrahepatic cholestasis due to citrin deficiency,
+BMGC_DS11350,BMG_DS039715,,Birdshot Chorioretinopathy,Birdshot Chorioretinopathy,,,,DOID:0111079,birdshot chorioretinopathy,C1853959,D000080365,605808,MONDO:0011599,birdshot chorioretinopathy,
+BMGC_DS11351,BMG_DS039716,,"DERMATITIS, ATOPIC, 4",,,,,DOID:0110100,atopic dermatitis 4,C1853963,,605805,MONDO:0011598,"dermatitis, atopic, 4",
+BMGC_DS11352,BMG_DS039718,,"Dermatitis, Atopic, 2",,,,,,,C1853965,C565293,605803,MONDO:0011596,"dermatitis, atopic, 2",
+BMGC_DS11353,BMG_DS039720,,"SEIZURES, BENIGN FAMILIAL INFANTILE, 2",,,,,DOID:0081115,benign familial infantile seizures 2,C1853995,,605751;614386,MONDO:0011593,"seizures, benign familial infantile, 2",
+BMGC_DS11354,BMG_DS039721,,EXUDATIVE VITREORETINOPATHY 3,,,,,,,C1854002,,605750,MONDO:0011592,exudative vitreoretinopathy 3,
+BMGC_DS11355,BMG_DS039725,,"Cataract, Central Saccular, With Sutural Opacities",,,,,,,C1854021,C565301,605728,MONDO:0011587,cataract 25,
+BMGC_DS11356,BMG_DS039726,,OTOSCLEROSIS 2,,,,,DOID:0060921,otosclerosis 2,C1854022,,605727,MONDO:0011586,otosclerosis 2,
+BMGC_DS11357,BMG_DS039727,,"Spinal muscular atrophy, Jerash type",,,,,DOID:0111065,autosomal recessive distal hereditary motor neuronopathy 2,C1854023,C535715,605726,MONDO:0011585,autosomal recessive distal spinal muscular atrophy 2,
+BMGC_DS11358,BMG_DS039728,,"SPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE",,,,,DOID:0111194,autosomal dominant adult-onset proximal spinal muscular atrophy,C1854058,,182980;605704,MONDO:0008453,"adult-onset proximal spinal muscular atrophy, autosomal dominant",
+BMGC_DS11359,BMG_DS039730,,Cardiomyopathy dilated with woolly hair and keratoderma,,,,,DOID:0090128,Carvajal syndrome,C1854063,C535581,605676,MONDO:0011581,arrhythmogenic cardiomyopathy with wooly hair and keratoderma,
+BMGC_DS11360,BMG_DS039732,,Late-Onset Retinal Degeneration,,,,,DOID:0060869,late-onset retinal degeneration,C1854065,C565309,605670,MONDO:0011579,late-onset retinal degeneration,
+BMGC_DS11361,BMG_DS039734,,,,,,,,,C1854106,,605637,MONDO:0011577,"myopathy, proximal, and ophthalmoplegia",
+BMGC_DS11362,BMG_DS039735,,"Hyperaldosteronism, Familial, Type II",,,,,,,C1854107,C565312,605635,MONDO:0011576,familial hyperaldosteronism type II,
+BMGC_DS11363,BMG_DS039736,,Cerebrooculonasal Syndrome,,,,,,,C1854108,C565313,605627,MONDO:0011575,cerebrooculonasal syndrome,
+BMGC_DS11364,BMG_DS039738,,,,,,,,,C1854124,,605606,MONDO:0011573,"psoriasis 7, susceptibility to",
+BMGC_DS11365,BMG_DS039740,,"Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1",,,,,,,C1854146,C565316,605594,MONDO:0011571,"deafness, autosomal dominant 39, with dentinogenesis imperfecta 1",
+BMGC_DS11366,BMG_DS039741,,"Charcot-Marie-Tooth disease, Type 2B2",,,,,DOID:0110179,Charcot-Marie-Tooth disease type 2B2,C1854150,C537991,605589,MONDO:0011570,Charcot-Marie-Tooth disease type 2B2,
+BMGC_DS11367,BMG_DS039742,,"Charcot-Marie-Tooth disease, Type 2B1",,,,,DOID:0110156,Charcot-Marie-Tooth disease type 2B1,C1854154,C537990,605588,MONDO:0011569,Charcot-Marie-Tooth disease type 2B1,
+BMGC_DS11368,BMG_DS039743,,"Deafness, Autosomal Dominant 25",,,,,,,C1854158,C565319,605583,MONDO:0011568,autosomal dominant nonsyndromic hearing loss 25,
+BMGC_DS11369,BMG_DS039744,,"Cardiomyopathy, Dilated, 1K",,,,,,,C1854159,C565320,605582,MONDO:0011567,dilated cardiomyopathy 1K,
+BMGC_DS11370,BMG_DS039745,,,,,,,,,C1854170,,605572,MONDO:0011566,abdominal obesity-metabolic syndrome quantitative trait locus 2,
+BMGC_DS11371,BMG_DS039746,,Cone-Rod Dystrophy 8,,,,,DOID:0111014,cone-rod dystrophy 8,C1854180,C565322,605549,MONDO:0011564,cone-rod dystrophy 8,
+BMGC_DS11372,BMG_DS039748,,"Parkinson Disease 4, Autosomal Dominant Lewy Body",,,,,,,C1854182,C565324,605543,MONDO:0011562,autosomal dominant Parkinson disease 4,
+BMGC_DS11373,BMG_DS039749,,"ALZHEIMER DISEASE 6, LATE-ONSET",,,,,,,C1854187,,605526,MONDO:0011561,Alzheimer disease 6,
+BMGC_DS11374,BMG_DS039752,,Leber Congenital Amaurosis 6,,,,,DOID:0110329,Leber congenital amaurosis 6,C1854260,C565327,613826,MONDO:0013446,Leber congenital amaurosis 6,
+BMGC_DS11375,BMG_DS039753,,Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia,,,,,,,C1854273,C565328,,MONDO:0011555,radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome,
+BMGC_DS11376,BMG_DS039754,,"DEAFNESS, AUTOSOMAL RECESSIVE 26",,,,,,,C1854275,,604439;605428,MONDO:0011553,autosomal recessive nonsyndromic hearing loss 26,
+BMGC_DS11377,BMG_DS039756,723362004,Hypotrichosis simplex,,,,,,,C1854310,C537160,,MONDO:0018914,hypotrichosis simplex,Hereditary hypotrichosis simplex (disorder) | Hereditary hypotrichosis simplex | Hypotrichosis simplex
+BMGC_DS11378,BMG_DS039757,,"Cataract, posterior polar, 3",,,,,,,C1854311,C535343,605387,MONDO:0011547,cataract 31 multiple types,
+BMGC_DS11379,BMG_DS039758,,"Epilepsy, Nocturnal Frontal Lobe, Type 3",,,,,,,C1854335,C565334,605375,MONDO:0011545,autosomal dominant nocturnal frontal lobe epilepsy 3,
+BMGC_DS11380,BMG_DS039759,,PARAGANGLIOMAS 3,,,,,,,C1854336,,605373,MONDO:0011544,paragangliomas 3,
+BMGC_DS11381,BMG_DS039763,,"Cardiomyopathy, Dilated, 1J",,,,,,,C1854368,C565337,605362,MONDO:0011541,dilated cardiomyopathy 1J,
+BMGC_DS11382,BMG_DS039764,,Spinocerebellar ataxia 14,,,,,,,C1854369,C537196,605361,MONDO:0011540,spinocerebellar ataxia type 14,
+BMGC_DS11383,BMG_DS039765,,,,,,,,,C1854380,,605355,MONDO:0011539,nemaline myopathy 5,
+BMGC_DS11384,BMG_DS039766,,Frontoocular Syndrome,,,,,,,C1854405,C565340,605321,MONDO:0011538,frontoocular syndrome,
+BMGC_DS11385,BMG_DS039768,,MACROCEPHALY/AUTISM SYNDROME,,,,,,,C1854416,,601728;605309,MONDO:0011537,macrocephaly-autism syndrome,
+BMGC_DS11386,BMG_DS039769,,Optic Atrophy 4,,,,,DOID:0111440,optic atrophy 4,C1854430,C565343,605293,MONDO:0011536,optic atrophy 4,
+BMGC_DS11387,BMG_DS039770,,SPLIT-HAND/FOOT MALFORMATION 4,,,,,,,C1854442,,603273;605289,MONDO:0011535,split hand-foot malformation 4,
+BMGC_DS11388,BMG_DS039771,,"Neuropathy, hereditary motor and sensory, Russe type",,,,,,,C1854449,C535813,605285,MONDO:0011534,Charcot-Marie-Tooth disease type 4G,
+BMGC_DS11389,BMG_DS039772,,Tuberous Sclerosis 1,,,,,DOID:0080324,tuberous sclerosis 1,C1854465,C565346,191100,MONDO:0008612,tuberous sclerosis 1,
+BMGC_DS11390,BMG_DS039773,777998000,Temtamy preaxial brachydactyly syndrome,,,,,DOID:0050814,temtamy preaxial brachydactyly syndrome,C1854466,C536958,605282,MONDO:0011533,temtamy preaxial brachydactyly syndrome,Temtamy preaxial brachydactyly syndrome | Temtamy preaxial brachydactyly syndrome (disorder)
+BMGC_DS11391,BMG_DS039774,,"Spastic paraplegia 13, autosomal dominant",,,,,,,C1854467,C537485,605280,MONDO:0011532,hereditary spastic paraplegia 13,
+BMGC_DS11392,BMG_DS039775,,Noonan Syndrome 2,,,,,DOID:0060580,Noonan syndrome 2,C1854469,C548081,605275,MONDO:0011531,Noonan syndrome 2,
+BMGC_DS11393,BMG_DS039776,,"Mesomelic Dysplasia, Savarirayan Type",,,,,,,C1854470,C565349,605274,MONDO:0011530,"mesomelic dysplasia, Savarirayan type",
+BMGC_DS11394,BMG_DS039777,,Spinocerebellar ataxia 13,,,,,,,C1854488,C537195,605259,MONDO:0011529,spinocerebellar ataxia type 13,
+BMGC_DS11395,BMG_DS039778,,"Carney Complex, Type 2",Carney Complex,,,,DOID:0050471,Carney complex,C1854540,D056733,605244,MONDO:0011525,Carney complex type 2,
+BMGC_DS11396,BMG_DS039779,,"Spastic paraplegia 14, autosomal recessive",,,,,,,C1854568,C537486,605229,MONDO:0011522,hereditary spastic paraplegia 14,
+BMGC_DS11397,BMG_DS039781,,,,,,,,,C1854577,,605218,MONDO:0011520,"systemic lupus erythematosus, susceptibility to, 2",
+BMGC_DS11398,BMG_DS039782,,"DEAFNESS, AUTOSOMAL DOMINANT 23",,,,,,,C1854594,,605192;601205,MONDO:0011519,autosomal dominant nonsyndromic hearing loss 23,
+BMGC_DS11399,BMG_DS039783,763618001,Wiedemann Steiner syndrome,,,,,,,C1854630,,605130,MONDO:0011518,Wiedemann-Steiner syndrome,"Wiedemann Steiner syndrome | Hypertrichosis, short stature, facial dysmorphism, developmental delay syndrome | Wiedemann Steiner syndrome (disorder)"
+BMGC_DS11400,BMG_DS039784,,"Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy",,,,,,,C1854631,C565359,605115,MONDO:0011517,pseudohyperaldosteronism type 2,
+BMGC_DS11401,BMG_DS039786,,"Muscular Dystrophy, Adult-Onset, with Leukoencephalopathy",,,,,,,C1854646,C565361,253590,MONDO:0009674,"muscular dystrophy, adult-onset, with leukoencephalopathy",
+BMGC_DS11402,BMG_DS039788,,LETHAL CONGENITAL CONTRACTURE SYNDROME 1,,,,,DOID:0060559,lethal congenital contracture syndrome 1,C1854664,,253310;603371,MONDO:0009670,lethal congenital contracture syndrome 1,
+BMGC_DS11403,BMG_DS039789,,"MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE",,,,,,,C1854678,,100690;253290;100720;100730,MONDO:0009668,lethal multiple pterygium syndrome,
+BMGC_DS11404,BMG_DS039795,,Mucolipidosis III Gamma,,,,,DOID:0080678,mucolipidosis III gamma,C1854896,C565367,252605,MONDO:0009652,GNPTG-mucolipidosis,
+BMGC_DS11405,BMG_DS039798,,Monosomy 7 of Bone Marrow,,,,,,,C1854978,C565370,252270,MONDO:0009646,monosomy 7 myelodysplasia and leukemia syndrome 1,
+BMGC_DS11406,BMG_DS039799,,Monocyte Chemotactic Disorder,,,,,,,C1854982,C565371,252250,MONDO:0009645,chronic mucocutaneous candidiasis due to monocyte chemotactic disorder,
+BMGC_DS11407,BMG_DS039800,,"Molybdenum Cofactor Deficiency, Complementation Group A",,,,,DOID:0111164,molybdenum cofactor deficiency type A,C1854988,C565372,252150,MONDO:0009643,sulfite oxidase deficiency due to molybdenum cofactor deficiency type A,
+BMGC_DS11408,BMG_DS039801,,"Molybdenum Cofactor Deficiency, Complementation Group B",,,,,DOID:0111163,molybdenum cofactor deficiency type B,C1854989,C565373,252160,MONDO:0009644,sulfite oxidase deficiency due to molybdenum cofactor deficiency type B,
+BMGC_DS11409,BMG_DS039802,,"Molybdenum Cofactor Deficiency, Complementation Group C",,,,,DOID:0111166,molybdenum cofactor deficiency type C,C1854990,C565374,615501,MONDO:0014212,sulfite oxidase deficiency due to molybdenum cofactor deficiency type C,
+BMGC_DS11410,BMG_DS039803,,Mitochondrial Complex II Deficiency,,,,,DOID:0060537,mitochondrial complex II deficiency,C1855008,C565375,,,,
+BMGC_DS11411,BMG_DS039805,,Mitochondrial myopathy with lactic acidosis,,,,,,,C1855033,C537476,251950,MONDO:0016825,mitochondrial myopathy-lactic acidosis-deafness syndrome,
+BMGC_DS11412,BMG_DS039806,,Mitochondrial Myopathy with a Defect in Mitochondrial Protein Transport,,,,,,,C1855034,C565376,251945,MONDO:0009638,mitochondrial myopathy with a defect in mitochondrial-protein transport,
+BMGC_DS11413,BMG_DS039808,,"MICROPHTHALMIA, ISOLATED 1",,,,,,,C1855052,,251600,MONDO:0009631,isolated microphthalmia 1,
+BMGC_DS11414,BMG_DS039809,,"Microphthalmia, Isolated, with Coloboma 4",,,,,,,C1855053,C565378,251505,MONDO:0009630,"microphthalmia, isolated, with coloboma 4",
+BMGC_DS11415,BMG_DS039811,,ATAXIA-TELANGIECTASIA VARIANT V2,,,,,,,C1855057,,251260,,,
+BMGC_DS11416,BMG_DS039813,,Microcephaly with Chemotactic Defect and Transient Hypogammaglobulinemia,,,,,,,C1855078,C565381,251240,MONDO:0009620,Say-Barber-Miller syndrome,
+BMGC_DS11417,BMG_DS039814,,Microcephaly-Micromelia Syndrome,,,,,,,C1855079,C565382,251230,MONDO:0009619,microcephaly-micromelia syndrome,
+BMGC_DS11418,BMG_DS039815,719380003,Winship Viljoen Leary syndrome,,,,,,,C1855080,C536711,251220,MONDO:0009618,microcephaly-cardiomyopathy syndrome,Winship Viljoen Leary syndrome | Microcephalus cardiomyopathy syndrome (disorder) | Microcephalus cardiomyopathy syndrome | Microcephaly cardiomyopathy syndrome
+BMGC_DS11419,BMG_DS039816,,,,,,,,,C1855081,,251200,MONDO:0009617,"microcephaly 1, primary, autosomal recessive",
+BMGC_DS11420,BMG_DS039818,,Methylmalonyl-CoA Epimerase Deficiency,,,,,,,C1855100,C565386,251120,MONDO:0009615,methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency,
+BMGC_DS11421,BMG_DS039820,,Methylmalonic aciduria cblB type,,,,,,,C1855102,C537361,251110,MONDO:0009614,"methylmalonic aciduria, cblB type",
+BMGC_DS11422,BMG_DS039821,,Methylmalonic aciduria cblA type,,,,,,,C1855109,C537360,251100,MONDO:0009613,"methylmalonic aciduria, cblA type",
+BMGC_DS11423,BMG_DS039822,,Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency,,,,,DOID:0060740,methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency,C1855114,C565390,251000,MONDO:0009612,methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency,
+BMGC_DS11424,BMG_DS039823,,"Methylmalonic Aciduria, mut(0) Type",,,,,DOID:0060740,methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency,C1855115,C565390,,,,
+BMGC_DS11425,BMG_DS039824,,"Methylmalonic Aciduria, mut(-) Type",,,,,DOID:0060740,methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency,C1855116,C565390,,,,
+BMGC_DS11426,BMG_DS039825,,Methylmalonic aciduria,,,,,,,C1855119,,MTHU037634,,,
+BMGC_DS11427,BMG_DS039826,,3-Methylglutaconic Aciduria Type IV,,,,,DOID:0110006,3-methylglutaconic aciduria type 4,C1855126,C565393,250951,MONDO:0009611,3-methylglutaconic aciduria type 4,
+BMGC_DS11428,BMG_DS039827,,"Methylcobalamin Deficiency, CblG Type",,,,,,,C1855128,C565394,250940,MONDO:0009609,methylcobalamin deficiency type cblG,
+BMGC_DS11429,BMG_DS039828,,Roy Maroteaux Kremp syndrome,,,,,,,C1855164,C535875,250500,MONDO:0009602,"metaphyseal modeling abnormality, skin lesions, and spastic paraplegia",
+BMGC_DS11430,BMG_DS039830,,"Metaphyseal Dysostosis, Mental Retardation, and Conductive Deafness",,,,,,,C1855175,C565396,250420,MONDO:0009599,metaphyseal dysostosis-intellectual disability-conductive deafness syndrome,
+BMGC_DS11431,BMG_DS039831,,,,,,,,,C1855179,,,MONDO:0020373,early-onset anterior polar cataract,
+BMGC_DS11432,BMG_DS039832,,Metaphyseal Chondrodysplasia with Retinitis Pigmentosa,,,,,,,C1855188,C565398,250410,MONDO:0009598,metaphyseal chondrodysplasia-retinitis pigmentosa syndrome,
+BMGC_DS11433,BMG_DS039833,,"Metaphyseal Chondrodysplasia, Pena Type",,,,,,,C1855195,C565399,250300,MONDO:0009596,"metaphyseal chondrodysplasia, Pena type",
+BMGC_DS11434,BMG_DS039835,,"Spondylometaphyseal dysplasia, Sedaghatian type",,,,,DOID:0112298,spondylometaphyseal dysplasia Sedaghatian type,C1855229,C535798,250220,MONDO:0009593,"spondylometaphyseal dysplasia, Sedaghatian type",
+BMGC_DS11435,BMG_DS039837,,Pseudoarylsulfatase A Deficiency,,,,,,,C1855255,C565403,,,,
+BMGC_DS11436,BMG_DS039838,,Mesomelic Limb Shortening and Bowing,,,,,,,C1855273,C565404,249710,MONDO:0009589,mesomelic dwarfism-cleft palate-camptodactyly syndrome,
+BMGC_DS11437,BMG_DS039841,,,,,,,,,C1855304,,249500,MONDO:0009580,"intellectual disability, autosomal recessive 1",
+BMGC_DS11438,BMG_DS039842,720958002,Ter Haar syndrome,,,,,DOID:0111789,Frank-Ter Haar syndrome,C1855305,C537274,211170;249420,MONDO:0009579,Frank-Ter Haar syndrome,Frank-Ter Haar syndrome (disorder) | Frank-Ter Haar syndrome | Ter Haar syndrome
+BMGC_DS11439,BMG_DS039843,,Megalencephaly with Dysmyelination,,,,,,,C1855309,C565408,249240,MONDO:0009574,megalencephaly with dysmyelination,
+BMGC_DS11440,BMG_DS039844,,Megaepiphyseal dwarfism,,,,,,,C1855310,C536140,249230,MONDO:0009573,megaepiphyseal dwarfism,
+BMGC_DS11441,BMG_DS039846,,MAST SYNDROME,,,,,,,C1855346,,248900;608181,MONDO:0009568,mast syndrome,
+BMGC_DS11442,BMG_DS039850,,"Maple Syrup Urine Disease, Type IA",,,,,,,C1855369,C535710,248600,MONDO:0023691,maple syrup urine disease type 1A,
+BMGC_DS11443,BMG_DS039851,,"MAPLE SYRUP URINE DISEASE, TYPE II",,,,,,,C1855371,,248610;620699,MONDO:0023693,maple syrup urine disease type 2,
+BMGC_DS11444,BMG_DS039855,,Marles Greenberg Persaud syndrome,,,,,,,C1855425,C536022,248450,MONDO:0009560,oculotrichoanal syndrome,
+BMGC_DS11445,BMG_DS039857,,"Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive",,,,,,,C1855433,C535707,248390,MONDO:0009558,Treacher Collins syndrome 3,
+BMGC_DS11446,BMG_DS039859,,,,,,,,,C1855464,,248260,MONDO:0009551,"magnesium, elevated red cell",
+BMGC_DS11447,BMG_DS039860,,Stargardt Disease 1,Stargardt Disease,,,,DOID:0050817,Stargardt disease,C1855465,D000080362,248200,MONDO:0009549,severe early-childhood-onset retinal dystrophy,
+BMGC_DS11448,BMG_DS039861,,"Hypomagnesemia 5, Renal, with Ocular Involvement",,,,,,,C1855466,C565423,,,,
+BMGC_DS11449,BMG_DS039864,,"Lymphopenic Hypergammaglobulinemia, Antibody Deficiency, Autoimmune Hemolytic Anemia, and Glomerulonephritis",,,,,,,C1855470,C565427,247800,MONDO:0009541,"lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis",
+BMGC_DS11450,BMG_DS039865,,Lymphokine Deficiency,,,,,,,C1855471,C565428,247650,MONDO:0009540,chronic mucocutaneous candidiasis due to lymphokine deficiency,
+BMGC_DS11451,BMG_DS039866,,,,,,,,,C1855472,,247640,MONDO:0009539,"lymphoblastic leukemia, acute, with lymphomatous features",
+BMGC_DS11452,BMG_DS039868,,"Lymphoblastic Transformation, Intrinsic Defect in",,,,,,,C1855474,C565431,247450,MONDO:0009536,chronic mucocutaneous candidiasis due to intrinsic defect in lymphoblastic transformation,
+BMGC_DS11453,BMG_DS039870,,,,,,,,,C1855476,,247430,MONDO:0009534,chronic mucocutaneous candidiasis due to inhibition of lymphoblastic transformation,
+BMGC_DS11454,BMG_DS039871,721083007,Dahlberg Borer Newcomer syndrome,,,,,,,C1855477,C535769,247410,MONDO:0009533,Dahlberg-Borer-Newcomer syndrome,Lymphedema hypoparathyroidism syndrome (disorder) | Lymphedema hypoparathyroidism syndrome | Lymphoedema hypoparathyroidism syndrome | Dahlberg Borer Newcomer syndrome | Dahlberg syndrome
+BMGC_DS11455,BMG_DS039872,,Lipase deficiency combined,,,,,,,C1855498,C535904,246650,MONDO:0009527,"lipase deficiency, combined",
+BMGC_DS11456,BMG_DS039873,,"Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome",,,,,,,C1855499,C565436,246570,MONDO:0009526,"fibular aplasia, tibial campomelia, and oligosyndactyly syndrome",
+BMGC_DS11457,BMG_DS039874,,"Limb Defects, Distal Transverse, with Mental Retardation and Spasticity",,,,,,,C1855501,C565438,246555,MONDO:0009524,intellectual disability-spasticity-ectrodactyly syndrome,
+BMGC_DS11458,BMG_DS039876,,"Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis",,,,,,,C1855504,C565440,246500,MONDO:0009522,Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome,
+BMGC_DS11459,BMG_DS039877,,,,,,,,,C1855505,,246470,MONDO:0009521,"leukemia, acute myelocytic, with polyposis coli and colon cancer",
+BMGC_DS11460,BMG_DS039878,,"Leg, Absence Deformity of, with Congenital Cataract",,,,,,,C1855523,C565442,246000,MONDO:0009516,absence deformity of leg-cataract syndrome,
+BMGC_DS11461,BMG_DS039879,,"Larsen like syndrome, lethal type",,,,,,,C1855535,C537872,245650,MONDO:0009512,lethal Larsen-like syndrome,
+BMGC_DS11462,BMG_DS039880,,Laron syndrome type 2,,,,,,,C1855548,C537871,,,,
+BMGC_DS11463,BMG_DS039881,,Lambotte syndrome,,,,,,,C1855550,C537549,245552,MONDO:0009508,Lambotte syndrome,
+BMGC_DS11464,BMG_DS039882,732961003,Lambert syndrome,,,,,,,C1855551,C538396,245550,MONDO:0009507,Lambert syndrome,"Lambert syndrome | Branchial dysplasia, intellectual disability, inguinal hernia syndrome (disorder) | Branchial dysplasia, intellectual disability, inguinal hernia syndrome"
+BMGC_DS11465,BMG_DS039883,,Lactic Aciduria due to D-Lactic Acid,,,,,,,C1855552,C565446,,,,
+BMGC_DS11466,BMG_DS039884,,Pyruvate Dehydrogenase E3-Binding Protein Deficiency,,,,,,,C1855553,C565447,245349,MONDO:0009503,pyruvate dehydrogenase E3-binding protein deficiency,
+BMGC_DS11467,BMG_DS039885,,Pyruvate Dehydrogenase E2 Deficiency,,,,,,,C1855565,C565448,245348,MONDO:0009502,pyruvate dehydrogenase E2 deficiency,
+BMGC_DS11468,BMG_DS039886,,Erythrocyte Lactate Transporter Defect,,,,,,,C1855577,C565449,245340,MONDO:0009501,metabolic myopathy due to lactate transporter defect,
+BMGC_DS11469,BMG_DS039887,,"KURU, SUSCEPTIBILITY TO",,,,,,,C1855588,,245300,MONDO:0009500,"kuru, susceptibility to",
+BMGC_DS11470,BMG_DS039890,724208006,Keutel syndrome,,,,,,,C1855607,C536167,245150,MONDO:0009495,Keutel syndrome,"Keutel syndrome (disorder) | Keutel syndrome | Pulmonic stenosis, brachytelephalangism, calcification of cartilage syndrome"
+BMGC_DS11471,BMG_DS039892,,HAIM-MUNK SYNDROME,,,,,,,C1855627,,245010;602365,MONDO:0009491,Haim-Munk syndrome,
+BMGC_DS11472,BMG_DS039893,,"Keratoderma, Palmoplantar, Norrbotten Recessive Type",,,,,DOID:0060862,mal de Meleda,C1855644,C565454,,,,
+BMGC_DS11473,BMG_DS039894,,Keratoconus posticus circumscriptus,,,,,,,C1855645,C536151,244600,MONDO:0009488,keratoconus posticus circumscriptus,
+BMGC_DS11474,BMG_DS039897,,"KENNY-CAFFEY SYNDROME, TYPE 1",,,,,DOID:0080722,Kenny-Caffey syndrome type 1,C1855648,,604934;244460,MONDO:0009486,autosomal recessive Kenny-Caffey syndrome,
+BMGC_DS11475,BMG_DS039898,722056009,Kaufman oculocerebrofacial syndrome,,,,,DOID:0111456,Kaufman oculocerebrofacial syndrome,C1855663,C537013,244450,MONDO:0009485,"oculocerebrofacial syndrome, Kaufman type",Oculocerebrofacial syndrome Kaufman type (disorder) | Oculocerebrofacial syndrome Kaufman type | Kaufman oculocerebrofacial syndrome
+BMGC_DS11476,BMG_DS039899,721862000,Arima syndrome,,,,,,,C1855675,C537430,243910,MONDO:0009480,Joubert syndrome with oculorenal defect,Joubert syndrome with oculorenal defect (disorder) | Joubert syndrome with oculorenal defect | Arima syndrome | Cerebello-oculo-renal syndrome
+BMGC_DS11477,BMG_DS039900,,"Nephronophthisis, familial juvenile",,,,,,,C1855681,C537699,256100,MONDO:0009728,nephronophthisis 1,
+BMGC_DS11478,BMG_DS039901,,Jejunal Atresia with Microcephaly and Ocular Anomalies,,,,,,,C1855705,C565460,616369;243605,MONDO:0009477,Stromme syndrome,
+BMGC_DS11479,BMG_DS039902,,,,,,,,,C1855714,,243450,MONDO:0009474,"isovaleric acid, inability to smell",
+BMGC_DS11480,BMG_DS039903,,"Intrinsic Factor and R Binder, Combined Congenital Deficiency of",,,,,,,C1855721,C565461,243320,MONDO:0009471,"intrinsic factor and r binder, combined congenital deficiency of",
+BMGC_DS11481,BMG_DS039904,,BARAITSER-WINTER SYNDROME 1,,,,,DOID:0081112,Baraitser-Winter syndrome 1,C1855722,,102630;243310,MONDO:0009470,Baraitser-Winter syndrome 1,
+BMGC_DS11482,BMG_DS039905,,Intestinal Pseudoobstruction with Patent Ductus Arteriosus and Natal Teeth,,,,,,,C1855732,C538341,243185,MONDO:0009467,natal teeth-intestinal pseudoobstruction-patent ductus syndrome,
+BMGC_DS11483,BMG_DS039906,,Neuronal intestinal pseudoobstruction,,,,,,,C1855733,C537394,243180,MONDO:8000011,"visceral neuropathy, familial, 1, autosomal recessive",
+BMGC_DS11484,BMG_DS039907,,IMMUNODEFICIENCY WITH DEFECTIVE T-CELL RESPONSE TO INTERLEUKIN 1,,,,,,,C1855735,,243110,MONDO:0009464,immunodeficiency with defective T-cell response to interleukin 1,
+BMGC_DS11485,BMG_DS039908,,,,,,,,,C1855736,,243100,MONDO:0009463,"internal carotid arteries, hypoplasia of",
+BMGC_DS11486,BMG_DS039909,,"Inosine Phosphorylase Deficiency, Immune Defect Due To",,,,,,,C1855737,C565465,243080,MONDO:0009462,"inosine phosphorylase deficiency, immune defect due to",
+BMGC_DS11487,BMG_DS039910,,Indolylacroyl Glycinuria with Mental Retardation,,,,,,,C1855738,C565466,243050,MONDO:0009460,indolylacroyl glycinuria with intellectual disability,
+BMGC_DS11488,BMG_DS039911,,"Indifference to Pain, Congenital, Autosomal Recessive",,,,,,,C1855739,C565467,243000,MONDO:0009459,"channelopathy-associated congenital insensitivity to pain, autosomal recessive",
+BMGC_DS11489,BMG_DS039912,,,,,,,,,C1855761,,242890,MONDO:0009457,"immunoglobulin d level in plasma, low",
+BMGC_DS11490,BMG_DS039915,,Absent corpus callosum cataract immunodeficiency,,,,,DOID:0060356,Vici syndrome,C1855772,C535566,242840,MONDO:0009452,Vici syndrome,
+BMGC_DS11491,BMG_DS039916,,"Ichthyosis, Split Hairs, and Amino Aciduria",,,,,,,C1855786,C565471,242550,MONDO:0009447,"ichthyosis, split hairs, and amino aciduria",
+BMGC_DS11492,BMG_DS039917,,"Ichthyosis, mental retardation, dwarfism, and renal impairment",,,,,,,C1855787,C536274,242530,MONDO:0009446,ichthyosis-intellectual disability-dwarfism-renal impairment syndrome,
+BMGC_DS11493,BMG_DS039918,,Jagell Holmgren Hofer syndrome,,,,,,,C1855788,C537364,242510,MONDO:0009444,ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome,
+BMGC_DS11494,BMG_DS039919,,Self-Healing Collodion Baby,,,,,,,C1855789,C565473,,MONDO:0017267,self-healing collodion baby,
+BMGC_DS11495,BMG_DS039920,,"Hypouricemia, Hypercalcinuria, and Decreased Bone Density",,,,,,,C1855793,C565475,242050,MONDO:0009438,"hypouricemia, hypercalcinuria, and decreased bone density",
+BMGC_DS11496,BMG_DS039921,,Bamforth syndrome,,,,,,,C1855794,C537901,241850,MONDO:0009437,Bamforth-Lazarus syndrome,
+BMGC_DS11497,BMG_DS039922,,"Hypoproteinemia, Hypercatabolic",,,,,DOID:0111981,immunodeficiency 43,C1855796,C565476,241600,MONDO:0009434,"hypoproteinemia, hypercatabolic",
+BMGC_DS11498,BMG_DS039925,1197148005,"Hypoparathyroidism, intellectual disability, dysmorphism syndrome",,,,,DOID:0060348,hypoparathyroidism-retardation-dysmorphism syndrome,C1855840,,241410,MONDO:0009426,hypoparathyroidism-retardation-dysmorphism syndrome,"Sanjad Sakati syndrome (disorder) | Richardson Kirk syndrome | Hypoparathyroidism, short stature, intellectual disability, seizures syndrome | Hypoparathyroidism, intellectual disability, dysmorphism syndrome | Sanjad Sakati syndrome | SSS - Sanjad Sakati syndrome"
+BMGC_DS11499,BMG_DS039927,,,,,,,,,C1855848,,241310,MONDO:0009425,hypomandibular faciocranial dysostosis,
+BMGC_DS11500,BMG_DS039928,,"Bartter syndrome, antenatal , type 2",,,,,,,C1855849,C537651,241200,MONDO:0009424,Bartter disease type 2,
+BMGC_DS11501,BMG_DS039929,,Hypohidrosis with Abnormal Palmar Dermal Ridges,,,,,,,C1855856,C565481,241120,MONDO:0009422,hypohidrosis with abnormal palmar dermal Ridges,
+BMGC_DS11502,BMG_DS039930,,Hypogonadism with Low-Grade Mental Deficiency and Microcephaly,,,,,,,C1855858,C565482,241000,MONDO:0009418,hypogonadism with low-grade mental deficiency and microcephaly,
+BMGC_DS11503,BMG_DS039931,,HYPOGONADISM-CATARACT SYNDROME,,,,,,,C1855859,,240950,MONDO:0009417,hypergonadotropic hypogonadism-cataract syndrome,
+BMGC_DS11504,BMG_DS039932,,"Glycogen Storage Disease 0, Liver",,,,,,,C1855861,C565485,240600,MONDO:0009414,glycogen storage disorder due to hepatic glycogen synthase deficiency,
+BMGC_DS11505,BMG_DS039933,,"Polyglandular Deficiency Syndrome, Persian-Jewish Type",,,,,,,C1855868,C538275,,,,
+BMGC_DS11506,BMG_DS039934,,"Autoimmune Polyendocrinopathy Syndrome, Type I, Autosomal Dominant",,,,,,,C1855869,C538275,,,,
+BMGC_DS11507,BMG_DS039936,,"Hyperuricemia, Infantile, with Abnormal Behavior and Normal Hypoxanthine Guanine Phosphoribosyltransferase",,,,,,,C1855884,C565489,240000,MONDO:0009408,"hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase",
+BMGC_DS11508,BMG_DS039937,,Hypertrophic Neuropathy And Cataract,,,,,,,C1855885,C565490,239900,MONDO:0009407,hypertrophic neuropathy and cataract,
+BMGC_DS11509,BMG_DS039938,1010628009,X-linked congenital generalized hypertrichosis,,,,,,,C1855900,,,,,X-linked congenital generalized hypertrichosis | X-linked congenital generalized hypertrichosis (disorder) | X-linked congenital generalised hypertrichosis | Congenital generalised hypertrichosis Macias-Flores type | Congenital generalized hypertrichosis Macias-Flores type | Macias-Flores Garcia-Cruz Rivera syndrome
+BMGC_DS11510,BMG_DS039939,,"Hypertrichosis, Congenital Anterior Cervical, with Peripheral Sensory and Motor Neuropathy",,,,,,,C1855902,C565492,239840,MONDO:0009405,cervical hypertrichosis-peripheral neuropathy syndrome,
+BMGC_DS11511,BMG_DS039940,,Hypertelorism and tetralogy of Fallot,,,,,,,C1855903,C538386,239711,MONDO:0009403,hypertelorism and tetralogy of fallot,
+BMGC_DS11512,BMG_DS039941,,Naguib-Richieri-Costa syndrome,,,,,,,C1855904,C538332,239710,MONDO:0009402,acrofrontofacionasal dysostosis 2,
+BMGC_DS11513,BMG_DS039943,33982008,Hyperphosphatasemia with intellectual disability,,,,,DOID:0070431,hyperphosphatasia with impaired intellectual development syndrome,C1855923,,,MONDO:0016596,hyperphosphatasia-intellectual disability syndrome,Hyperphosphatasemia with mental retardation | Hyperphosphatasaemia with mental retardation | Hyperphosphatasia with seizures and neurologic deficit | Mabry syndrome | Hyperphosphatasaemia with intellectual disability | Hyperphosphatasemia with intellectual disability (disorder) | Hyperphosphatasemia with intellectual disability
+BMGC_DS11514,BMG_DS039944,,"Hyperparathyroidism, Neonatal Self-Limited Primary, With Hypercalciuria",,,,,,,C1855924,C565496,239199,MONDO:0009396,"hyperparathyroidism, neonatal self-limited primary, with hypercalciuria",
+BMGC_DS11515,BMG_DS039945,,,,,,,,,C1855925,,238950,MONDO:0009392,"hyperopia, high",
+BMGC_DS11516,BMG_DS039947,,Hyperlysinemia Due To Defect In Lysine Transport Into Mitochondria,,,,,,,C1855927,C565499,238710,MONDO:0009389,hyperlysinemia due to defect in lysine transport into mitochondria,
+BMGC_DS11517,BMG_DS039948,,,,,,,,,C1855928,,238350,MONDO:0009386,hyperlexia,
+BMGC_DS11518,BMG_DS039949,,,,,,,,,C1855986,,236900,MONDO:0009373,seizures-intellectual disability due to hydroxylysinuria syndrome,
+BMGC_DS11519,BMG_DS039950,,L-2-HYDROXYGLUTARIC ACIDURIA,,,,,DOID:0050574,L-2-hydroxyglutaric aciduria,C1855995,,609584;236792,MONDO:0009370,L-2-hydroxyglutaric aciduria,
+BMGC_DS11520,BMG_DS039952,,HYDROLETHALUS SYNDROME 1,,,,,,,C1856016,,610693;236680,MONDO:0009365,hydrolethalus syndrome 1,
+BMGC_DS11521,BMG_DS039953,732926009,Daish Hardman Lamont syndrome,,,,,,,C1856051,C535770,236660,MONDO:0009363,hydrocephaly-tall stature-joint laxity syndrome,"Hydrocephalus, tall stature, joint laxity syndrome (disorder) | Hydrocephalus, tall stature, joint laxity syndrome | Daish Hardman Lamont syndrome | Hydrocephaly, tall stature, joint laxity syndrome"
+BMGC_DS11522,BMG_DS039955,,Hydranencephaly with Renal Aplasia-Dysplasia,,,,,,,C1856053,C565507,236500,MONDO:0009359,multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome,
+BMGC_DS11523,BMG_DS039956,,HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME,,,,,,,C1856054,,236450,MONDO:0009358,Hutterite cerebroosteonephrodysplasia syndrome,
+BMGC_DS11524,BMG_DS039957,,Humeroradial Multiple Synostosis Syndrome,,,,,,,C1856055,C565509,236400,MONDO:0009356,autosomal recessive humeroradial synostosis,
+BMGC_DS11525,BMG_DS039958,,"Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type",,,,,,,C1856057,C565510,236270,MONDO:0009354,methylcobalamin deficiency type cblE,
+BMGC_DS11526,BMG_DS039960,,Methylenetetrahydrofolate reductase deficiency,,,,E72.12,,,C1856061,C537357,MTHU012414;236250,MONDO:0009353,homocystinuria due to methylene tetrahydrofolate reductase deficiency,
+BMGC_DS11527,BMG_DS039961,783159001,Holzgreve Wagner Rehder syndrome,,,,,DOID:0060566,Holzgreve-Wagner-Rehder Syndrome,C1856095,C535327,236110,MONDO:0009350,Holzgreve-Wagner-Rehder syndrome,"Holzgreve Wagner Rehder syndrome | Cleft palate, Potter sequence, congenital heart anomalies, mesoaxial polydactyly, multiple malformations syndrome | Holzgreve syndrome (disorder) | Holzgreve syndrome"
+BMGC_DS11528,BMG_DS039962,,Al Gazali Hirschsprung syndrome,,,,,,,C1856110,C535615,235760,MONDO:0009344,Hirschsprung disease-nail hypoplasia-dysmorphism syndrome,
+BMGC_DS11529,BMG_DS039963,,"Hirschsprung Disease with Ulnar Polydactyly, Polysyndactyly of Big Toes, and Ventricular Septal Defect",,,,,,,C1856111,C565517,235750,MONDO:0009343,"Hirschsprung disease with ulnar polydactyly, polysyndactyly of big toes, and ventricular septal defect",
+BMGC_DS11530,BMG_DS039964,,"Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness",,,,,,,C1856112,C565518,235740,MONDO:0009342,Hirschsprung disease-hearing loss-polydactyly syndrome,
+BMGC_DS11531,BMG_DS039965,703535000,Mowat-Wilson syndrome,,,,,DOID:0060485,Mowat-Wilson syndrome,C1856113,C536990,235730,MONDO:0009341,Mowat-Wilson syndrome,Mowat-Wilson syndrome (disorder) | Mowat-Wilson syndrome | Hirschsprung disease-mental retardation syndrome | Hirschsprung disease-intellectual disability syndrome
+BMGC_DS11532,BMG_DS039966,,"Bile acid synthesis defect, congenital, 2",,,,,DOID:0111069,congenital bile acid synthesis defect 2,C1856127,C535443,235555,MONDO:0009339,congenital bile acid synthesis defect 2,
+BMGC_DS11533,BMG_DS039967,,Hepatic venoocclusive disease with immunodeficiency,,,,,DOID:0112254,hepatic venoocclusive disease with immunodeficiency,C1856128,C537257,235550,MONDO:0009338,hepatic veno-occlusive disease-immunodeficiency syndrome,
+BMGC_DS11534,BMG_DS039969,,Hemolytic Anemia with Thermal Sensitivity of Red Cells,,,,,,,C1856158,C565522,235370,MONDO:0009334,hemolytic anemia with thermal sensitivity of red cells,
+BMGC_DS11535,BMG_DS039970,,Urioste Martinez-Frias syndrome,,,,,,,C1856159,C536478,235255,MONDO:0009333,mullerian derivatives-lymphangiectasia-polydactyly syndrome,
+BMGC_DS11536,BMG_DS039971,,"HEMIHYPERPLASIA, ISOLATED",,,,,,,C1856184,,235000,MONDO:0009331,isolated hemihyperplasia,
+BMGC_DS11537,BMG_DS039972,,Deafness enamel hypoplasia nail defects,,,,,,,C1856186,C535994,,MONDO:0100229,obsolete Heimler syndrome,
+BMGC_DS11538,BMG_DS039973,771180005,Kleiner Holmes syndrome,,,,,,,C1856197,C536885,234280,MONDO:0009321,hallux varus-preaxial polysyndactyly syndrome,"Kleiner Holmes syndrome | Hallux varus, preaxial polysyndactyly syndrome | Hallux varus, preaxial polysyndactyly syndrome (disorder)"
+BMGC_DS11539,BMG_DS039974,,Hall Riggs mental retardation syndrome,,,,,,,C1856198,C535623,234250,MONDO:0009320,Hall-Riggs syndrome,
+BMGC_DS11540,BMG_DS039975,,Hair defect with photosensitivity and mental retardation,,,,,,,C1856241,C537628,234030,MONDO:0022316,hair defect with photosensitivity and intellectual disability syndrome,
+BMGC_DS11541,BMG_DS039977,,Grouped Pigmentation of the Macula,,,,,,,C1856244,C565530,233800,MONDO:0009311,grouped pigmentation of the retina,
+BMGC_DS11542,BMG_DS039978,,"Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II",,,,,,,C1856245,C565531,233710,MONDO:0009310,"granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2",
+BMGC_DS11543,BMG_DS039979,,"Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I",,,,,,,C1856251,C565532,233700,MONDO:0009309,"granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 1",
+BMGC_DS11544,BMG_DS039980,,"GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 4",,,,,DOID:0070193,autosomal recessive chronic granulomatous disease 4,C1856255,,233690;608508,MONDO:0009308,"granulomatous disease, chronic, autosomal recessive, cytochrome b-negative",
+BMGC_DS11545,BMG_DS039981,,Granulomatous Disease with Defect in Neutrophil Chemotaxis,,,,,,,C1856261,C565534,233670,MONDO:0009307,granulomatous disease with defect in neutrophil chemotaxis,
+BMGC_DS11546,BMG_DS039982,,Granulocytopenia with Immunoglobulin Abnormality,,,,,DOID:0111974,immunodeficiency 59,C1856263,C565535,233600,MONDO:0009305,granulocytopenia with immunoglobulin abnormality,
+BMGC_DS11547,BMG_DS039984,,,,,,,,,C1856273,,233420,MONDO:0009301,"46,XY sex reversal 7",
+BMGC_DS11548,BMG_DS039985,,GOMBO syndrome,,,,,,,C1856274,C537284,233270,MONDO:0009298,GOMBO syndrome,
+BMGC_DS11549,BMG_DS039986,,Glycoprotein Storage Disease,,,,,,,C1856275,C565538,232900,MONDO:0009296,glycoprotein storage disease,
+BMGC_DS11550,BMG_DS039987,,"GSD IV, Classic Hepatic",,,,,,,C1856301,C565539,,,,
+BMGC_DS11551,BMG_DS039989,,"GSD IV, Neuromuscular Form, Fatal Perinatal",,,,,,,C1856303,C565541,,MONDO:0017697,"glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form",
+BMGC_DS11552,BMG_DS039990,,"GSD IV, Neuromuscular Form, Congenital",,,,,,,C1856304,C565542,,MONDO:0017698,"glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form",
+BMGC_DS11553,BMG_DS039991,,"GSD IV, Neuromuscular Form, Childhood",,,,,,,C1856305,C565543,,MONDO:0017700,"glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form",
+BMGC_DS11554,BMG_DS039994,,"Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to",,,,,DOID:0080699,glutathione synthetase deficiency,C1856399,C536835,231900,MONDO:0009284;MONDO:0017909,inherited glutathione synthetase deficiency | glutathione synthetase deficiency without 5-oxoprolinuria,
+BMGC_DS11555,BMG_DS039995,,Glutaric Aciduria IIA,Multiple Acyl Coenzyme A Dehydrogenase Deficiency,,,,DOID:0060358,multiple acyl-CoA dehydrogenase deficiency,C1856401,D054069,,,,
+BMGC_DS11556,BMG_DS039996,,Glutaric Aciduria IIB,Multiple Acyl Coenzyme A Dehydrogenase Deficiency,,,,DOID:0060358,multiple acyl-CoA dehydrogenase deficiency,C1856403,D054069,,,,
+BMGC_DS11557,BMG_DS039997,,Glutaric Aciduria IIC,Multiple Acyl Coenzyme A Dehydrogenase Deficiency,,,,DOID:0060358,multiple acyl-CoA dehydrogenase deficiency,C1856405,D054069,,,,
+BMGC_DS11558,BMG_DS039998,,"GLAUCOMA 3, PRIMARY CONGENITAL, A",,,,,,,C1856439,,601771;231300,MONDO:0009277,glaucoma 3A,
+BMGC_DS11559,BMG_DS040001,,"Bernard-Soulier Syndrome, Type B",,,,,,,C1856447,C565549,,,,
+BMGC_DS11560,BMG_DS040002,,"Bernard-Soulier Syndrome, Type C",,,,,,,C1856448,C565550,,,,
+BMGC_DS11561,BMG_DS040003,,,,,,,,,C1856465,,231095,MONDO:0009274,ghosal hematodiaphyseal dysplasia,
+BMGC_DS11562,BMG_DS040004,,Genito palato cardiac syndrome,,,,,,,C1856466,C537683,231060,MONDO:0009270,genito-palato-cardiac syndrome,
+BMGC_DS11563,BMG_DS040005,,"Gaucher Disease, Type Iiic",,,,,,,C1856476,C565553,231005,MONDO:0009268,Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,
+BMGC_DS11564,BMG_DS040009,,"Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to",,,,,DOID:0111681,congenital nonspherocytic hemolytic anemia 7,C1856603,C565557,230450,MONDO:0009259,gamma-glutamylcysteine synthetase deficiency,
+BMGC_DS11565,BMG_DS040010,,Fructose and Galactose Intolerance,,,,,,,C1856686,C565558,229500,MONDO:0009248,fructose and galactose intolerance,
+BMGC_DS11566,BMG_DS040012,,FRIEDREICH ATAXIA 1,,,,,,,C1856689,,229300,MONDO:0100340,Friedreich ataxia 1,
+BMGC_DS11567,BMG_DS040014,,Fraser-Like Syndrome,,,,,,,C1856708,C565562,229230,MONDO:0009243,Fraser-like syndrome,
+BMGC_DS11568,BMG_DS040015,,"Follicle-stimulating hormone deficiency, isolated",,,,,,,C1856716,C537070,,,,
+BMGC_DS11569,BMG_DS040016,,"Fleck Retina, Familial Benign",,,,,DOID:0111677,familial benign fleck retina,C1856718,C565564,228980,MONDO:0009235,familial benign flecked retina,
+BMGC_DS11570,BMG_DS040017,,"Kininogen Deficiency, Total",,,,,,,C1856719,C537060,,,,
+BMGC_DS11571,BMG_DS040019,721296004,Fuhrmann syndrome,,,,,DOID:0090067,Fuhrmann syndrome,C1856728,C538189,228930,MONDO:0009232,Fuhrmann syndrome,Fuhrmann syndrome (disorder) | Fuhrmann syndrome | Fuhrmann Rieger de Sousa syndrome
+BMGC_DS11572,BMG_DS040020,,Fibular hypoplasia and complex brachydactyly,,,,,DOID:0050790,fibular hypoplasia and complex brachydactyly,C1856738,C537931,228900,MONDO:0009231,acromesomelic dysplasia 2B,
+BMGC_DS11573,BMG_DS040023,,Femur bifid with monodactylous ectrodactyly,,,,,,,C1856789,C537917,228250,MONDO:0009222,Gollop-Wolfgang complex,
+BMGC_DS11574,BMG_DS040027,725434009,Autosomal recessive facio-digito-genital syndrome,,,,,,,C1856871,,227330,MONDO:0009209,autosomal recessive faciodigitogenital syndrome,Autosomal recessive faciodigitogenital syndrome (disorder) | Autosomal recessive facio-digito-genital syndrome | Aarskog-like syndrome | Autosomal recessive faciodigitogenital syndrome | Facio-digito-genital syndrome Kuwait type | Teebi Naguib Alawadi syndrome
+BMGC_DS11575,BMG_DS040028,,"Factor V And Factor VIII, Combined Deficiency Of, With Normal Protein C And Protein C Inhibitor",,,,,,,C1856882,C565577,227310,MONDO:0009207,"factor V and factor VIII, combined deficiency of, with normal protein C and protein C inhibitor",
+BMGC_DS11576,BMG_DS040029,,,,,,,,,C1856883,,,MONDO:0018175,combined deficiency of factor V and factor VIII,
+BMGC_DS11577,BMG_DS040030,,"Faciocardiomelic Dysplasia, Lethal",,,,,,,C1856891,C565578,227270,MONDO:0009204,lethal faciocardiomelic dysplasia,
+BMGC_DS11578,BMG_DS040031,,Facial Dysmorphism with Multiple Malformations,,,,,,,C1856892,C565579,227255,MONDO:0009202,Thakker-Donnai syndrome,
+BMGC_DS11579,BMG_DS040034,,"Eunuchoidism, familial hypogonadotropic",,,,,,,C1856897,C535764,227200;614841,MONDO:0013914,hypogonadotropic hypogonadism 12 with or without anosmia,
+BMGC_DS11580,BMG_DS040035,,,,,,,,,C1856898,,227090,MONDO:0009198,congenital lethal erythroderma,
+BMGC_DS11581,BMG_DS040036,,Ermine phenotype,,,,,,,C1856899,C535508,227010,MONDO:0009196,ermine phenotype,
+BMGC_DS11582,BMG_DS040037,,,,,,,,,C1856900,,227000,MONDO:0009195,erythema of acral regions,
+BMGC_DS11583,BMG_DS040039,,"Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness",,,,,,,C1856918,C565585,226950,MONDO:0009190,"epiphyseal dysplasia of femoral head, myopia, and deafness",
+BMGC_DS11584,BMG_DS040040,,Epilepsy telangiectasia,,,,,,,C1856929,C535497,226850,MONDO:0009188,epilepsy-telangiectasia syndrome,
+BMGC_DS11585,BMG_DS040041,,Epilepsy occipital calcifications,,,,,,,C1856930,C535496,226810,MONDO:0009187,celiac disease-epilepsy-cerebral calcification syndrome,
+BMGC_DS11586,BMG_DS040042,,"Epilepsy, Photogenic, with Spastic Diplegia and Mental Retardation",,,,,,,C1856931,C565587,226800,MONDO:0009186,"epilepsy, photogenic, with spastic diplegia and intellectual disability",
+BMGC_DS11587,BMG_DS040043,,Epidermolysis Bullosa With Diaphragmatic Hernia,,,,,,,C1856933,C565588,226735,MONDO:0009184,epidermolysis bullosa with diaphragmatic hernia,
+BMGC_DS11588,BMG_DS040044,,Epidermolysis bullosa with pyloric atresia,,,,,,,C1856934,C535377,,,,
+BMGC_DS11589,BMG_DS040047,,Endocardial Fibroelastosis and Coarctation of Abdominal Aorta,,,,,,,C1856971,C565592,226100,MONDO:0009170,endocardial fibroelastosis and coarctation of abdominal aorta,
+BMGC_DS11590,BMG_DS040048,,Encephaloclastic Proliferative Vasculopathy,,,,,DOID:0111666,proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome,C1856972,C565593,225790,MONDO:0009168,Fowler syndrome,
+BMGC_DS11591,BMG_DS040050,718608006,Pontocerebellar hypoplasia type 4,,,,,DOID:0060273,pontocerebellar hypoplasia type 4,C1856974,,225753,MONDO:0009166,pontocerebellar hypoplasia type 4,Congenital pontocerebellar hypoplasia type 4 (disorder) | Congenital pontocerebellar hypoplasia type 4 | PCH4 - pontocerebellar hypoplasia type 4 | Pontocerebellar hypoplasia type 4 | Fatal infantile encephalopathy with olivopontocerebellar hypoplasia
+BMGC_DS11592,BMG_DS040052,,"Encephalomalacia, Multilocular",,,,,,,C1856991,C565597,225700,MONDO:0009163,"encephalomalacia, multilocular",
+BMGC_DS11593,BMG_DS040055,,"Ehlers-Danlos syndrome, cardiac valvular form",,,,,,,C1857034,C536200,,,,
+BMGC_DS11594,BMG_DS040056,,Ehlers-Danlos Syndrome with Platelet Dysfunction from Fibronectin Abnormality,,,,,,,C1857038,C565600,225310,MONDO:0009158,"Ehlers-Danlos syndrome, fibronectinemic type",
+BMGC_DS11595,BMG_DS040057,,Ectrodactyly-Polydactyly,,,,,,,C1857040,C565601,225290,MONDO:0009156,ectrodactyly-polydactyly syndrome,
+BMGC_DS11596,BMG_DS040058,,"Ectodermal dysplasia, ectrodactyly, and macular dystrophy",,,,,,,C1857041,C536190,225280,MONDO:0009155,EEM syndrome,
+BMGC_DS11597,BMG_DS040059,,"Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia",,,,,,,C1857052,C565604,225050,MONDO:0009150,hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome,
+BMGC_DS11598,BMG_DS040061,,Ectodermal Dysplasia and Neurosensory Deafness,,,,,,,C1857068,C565606,224800,MONDO:0009146,ectodermal dysplasia-sensorineural deafness syndrome,
+BMGC_DS11599,BMG_DS040062,,Schopf-Schulz-Passarge Syndrome,,,,,DOID:0111647,Schopf-Schulz-Passarge syndrome,C1857069,C565607,224750,MONDO:0009145,SchC6pf-Schulz-Passarge syndrome,
+BMGC_DS11600,BMG_DS040065,,Dystonia musculorum deformans type 2,,,,,,,C1857093,C538006,224500,MONDO:0009141,torsion dystonia 2,
+BMGC_DS11601,BMG_DS040066,,Dyssegmental dysplasia,,,,,,,C1857100,C537998,224410;MTHU013285,MONDO:0009140,Silverman-Handmaker type dyssegmental dysplasia,
+BMGC_DS11602,BMG_DS040068,,"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1",,,,,DOID:0070015,autosomal recessive dyskeratosis congenita 1,C1857144,,224230;606471,MONDO:0009136,"dyskeratosis congenita, autosomal recessive 1",
+BMGC_DS11603,BMG_DS040069,,Dysautonomia like disorder,,,,,,,C1857153,C535728,224000,MONDO:0009132,dysautonomia-like disorder,
+BMGC_DS11604,BMG_DS040070,,"Dwarfism, Proportionate, with Hip Dislocation",,,,,,,C1857196,C565614,223550,MONDO:0009129,"dwarfism, proportionate, with hip dislocation",
+BMGC_DS11605,BMG_DS040071,,"Dwarfism, Low-Birth-Weight Type, with Unresponsiveness to Growth Hormone",,,,,,,C1857197,C565615,223500,MONDO:0009127,"dwarfism, low-birth-weight type, with unresponsiveness to growth hormone",
+BMGC_DS11606,BMG_DS040072,,,,,,,,,C1857225,,223350,MONDO:0009122,Dohle bodies and leukemia,
+BMGC_DS11607,BMG_DS040073,,DK Phocomelia Syndrome,,,,,,,C1857226,C565618,223340,MONDO:0009121,von Voss-Cherstvoy syndrome,
+BMGC_DS11608,BMG_DS040077,,"Rhizomelic chondrodysplasia punctata, type 2",,,,,DOID:0110852,rhizomelic chondrodysplasia punctata type 2,C1857242,C537607,222765,MONDO:0009112,rhizomelic chondrodysplasia punctata type 2,
+BMGC_DS11609,BMG_DS040078,,"2,4-Dienoyl-CoA Reductase Deficiency",,,,,,,C1857252,C565624,616034,MONDO:0014464,progressive encephalopathy with leukodystrophy due to DECR deficiency,
+BMGC_DS11610,BMG_DS040079,,Dicarboxylicaminoaciduria,,,,,DOID:0060650,dicarboxylic aminoaciduria,C1857253,C536171,222730,MONDO:0009110,dicarboxylic aminoaciduria,
+BMGC_DS11611,BMG_DS040080,,"Diastrophic Dysplasia, Broad Bone-Platyspondylic Variant",,,,,,,C1857255,C565626,,,,
+BMGC_DS11612,BMG_DS040081,,Trichohepatoenteric Syndrome,,,,,DOID:0111414,trichohepatoenteric syndrome,C1857276,C565627,,MONDO:0009105,trichohepatoenteric syndrome,
+BMGC_DS11613,BMG_DS040082,702418009,Donnai-Barrow syndrome,,,,,DOID:0090144,Donnai-Barrow syndrome,C1857277,C536390,222448,MONDO:0009104,Donnai-Barrow syndrome,Diaphragmatic hernia-exomphalos-hypertelorism syndrome (disorder) | Donnai-Barrow syndrome | Diaphragmatic hernia-exomphalos-corpus callosum agenesis | Diaphragmatic hernia-exomphalos-hypertelorism syndrome | Faciooculoacousticorenal syndrome
+BMGC_DS11614,BMG_DS040083,,,,,,,,,C1857284,,222400,MONDO:0009103,diaphragmatic hernia 2,
+BMGC_DS11615,BMG_DS040084,,Diaminopentanuria,,,,,,,C1857285,C565630,222350,MONDO:0009102,diaminopentanuria,
+BMGC_DS11616,BMG_DS040085,,"Diabetes Insipidus, Nephrogenic, with Mental Retardation and Intracerebral Calcification",,,,,,,C1857297,C565632,221995,MONDO:0009099,nephrogenic diabetes insipidus-intracranial calcification syndrome,
+BMGC_DS11617,BMG_DS040088,733044009,Dermatoleukodystrophy,,,,,,,C1857314,C538220,221790,MONDO:0009093,dermatoleukodystrophy,Dermatoleukodystrophy | Dermatoleukodystrophy (disorder)
+BMGC_DS11618,BMG_DS040089,,,,,,,DOID:0090112,Nasu-Hakola disease,C1857316,,,MONDO:0009092,polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly,
+BMGC_DS11619,BMG_DS040090,,"Deafness, Sensorineural, Autosomal-Mitochondrial Type",,,,,,,C1857332,C565637,221745,MONDO:0009090,"hearing loss, sensorineural, autosomal-mitochondrial type",
+BMGC_DS11620,BMG_DS040091,,Deafness oligodontia syndrome,,,,,,,C1857333,C538049,221740,MONDO:0009089,deafness-oligodontia syndrome,
+BMGC_DS11621,BMG_DS040092,,"Deafness, Neural, with Atypical Atopic Dermatitis",,,,,,,C1857334,C565639,221700,MONDO:0009088,"deafness, neural, with atypical atopic dermatitis",
+BMGC_DS11622,BMG_DS040093,,"Deafness, Neural, Congenital Moderate",,,,,,,C1857337,C565640,221500,MONDO:0009087,"deafness, neural, congenital moderate",
+BMGC_DS11623,BMG_DS040094,733071009,Groll Hirschowitz syndrome,,,,,,,C1857338,C537305,221400,MONDO:0009086,deafness-small bowel diverticulosis-neuropathy syndrome,"Deafness, small bowel diverticulosis, neuropathy syndrome (disorder) | Deafness, small bowel diverticulosis, neuropathy syndrome | Groll Hirschowitz syndrome"
+BMGC_DS11624,BMG_DS040095,,"Deafness, Congenital, with Vitiligo and Achalasia",,,,,,,C1857339,C565642,221350,MONDO:0009085,deafness-vitiligo-achalasia syndrome,
+BMGC_DS11625,BMG_DS040096,,Deafness conductive ptosis skeletal anomalies,,,,,,,C1857340,C535993,221320,MONDO:0009084,conductive deafness-ptosis-skeletal anomalies syndrome,
+BMGC_DS11626,BMG_DS040097,,"Deafness, Conductive, with Malformed External Ear",,,,,,,C1857341,C565644,221300,MONDO:0009083,conductive deafness-malformed external ear syndrome,
+BMGC_DS11627,BMG_DS040099,,"Deafness, Congenital, with Total Albinism",,,,,,,C1857343,C565646,220900,MONDO:0009081,"deafness, congenital, with total albinism",
+BMGC_DS11628,BMG_DS040100,,Split-Hand-Foot Malformation With Sensorineural Hearing Loss,,,,,,,C1857344,C565647,220600,MONDO:0009080,split hand-foot malformation 1 with sensorineural hearing loss,
+BMGC_DS11629,BMG_DS040102,,Dandy Walker malformation postaxial polydactyly,,,,,,,C1857351,C535771,220220,MONDO:0009075,Dandy-Walker malformation-postaxial polydactyly syndrome,
+BMGC_DS11630,BMG_DS040104,,"Leigh syndrome , French Canadian type",,,,,DOID:0111180,French Canadian Leigh disease,C1857355,C537004,220111,MONDO:0009069,"congenital lactic acidosis, Saguenay-Lac-Saint-Jean type",
+BMGC_DS11631,BMG_DS040105,,"Cystinuria, Type A",,,,,,,C1857388,C565652,,MONDO:0019745,cystinuria type A,
+BMGC_DS11632,BMG_DS040106,,"Cystinuria, Type B",,,,,,,C1857389,C565652,,MONDO:0019746,cystinuria type B,
+BMGC_DS11633,BMG_DS040108,,De Toni-Debre-Fanconi Syndrome,Fanconi Syndrome,,,,,,C1857395,D005198,,MONDO:0007600,primary Fanconi syndrome,
+BMGC_DS11634,BMG_DS040109,,Cystic Kidney Disease with Ventriculomegaly,,,,,DOID:0111625,ventriculomegaly - cystic kidney disease,C1857423,C565657,219730,MONDO:0009063,ventriculomegaly-cystic kidney disease,
+BMGC_DS11635,BMG_DS040111,,Cysteine Peptiduria,,,,,,,C1857438,C565659,219550,MONDO:0009059,cysteine Peptiduria,
+BMGC_DS11636,BMG_DS040113,,CUTIS VERTICIS GYRATA AND IMPAIRED INTELLECTUAL DEVELOPMENT,,,,,,,C1857444,,219300,MONDO:0009056,cutis verticis gyrata and intellectual disability,
+BMGC_DS11637,BMG_DS040114,,"Cutaneous photosensitivity and colitis, lethal",,,,,,,C1857449,C536224,219095,MONDO:0009051,cutaneous photosensitivity-lethal colitis syndrome,
+BMGC_DS11638,BMG_DS040115,,Acth-Independent Macronodular Adrenal Hyperplasia,,,,,,,C1857451,C565662,219080,MONDO:0020735,ACTH-independent macronodular adrenal hyperplasia 1,
+BMGC_DS11639,BMG_DS040116,,,,,,,,,C1857452,,219070,MONDO:0009048,curved nail of fourth toe,
+BMGC_DS11640,BMG_DS040118,,Craniosynostosis Mental Retardation Clefting Syndrome,,,,,,,C1857472,C565663,218650,MONDO:0009041,craniosynostosis-intellectual disability-clefting syndrome,
+BMGC_DS11641,BMG_DS040120,,Craniosynostosis with Fibular Aplasia,,,,,,,C1857492,C565665,218550,MONDO:0009038,craniosynostosis-fibular aplasia syndrome,
+BMGC_DS11642,BMG_DS040123,,Craniofacial dyssynostosis,,,,,,,C1857511,C536455,218350,MONDO:0009034,craniofacial dyssynostosis,
+BMGC_DS11643,BMG_DS040124,719947004,Temtamy syndrome,,,,,DOID:0111621,Temtamy syndrome,C1857512,C536959,218340,MONDO:0009033,temtamy syndrome,Temtamy syndrome | Temtamy Shalash syndrome | Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome (disorder) | Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome
+BMGC_DS11644,BMG_DS040125,,"Cranial Nerves, Recurrent Paresis Of",,,,,,,C1857530,C565672,218200,MONDO:0009030,"cranial nerves, recurrent paresis of",
+BMGC_DS11645,BMG_DS040126,,"Cranial Nerves, Congenital Paresis Of",,,,,,,C1857531,C565673,218100,MONDO:0009029,"cranial nerves, congenital paresis of",
+BMGC_DS11646,BMG_DS040128,,,,,,,,,C1857533,,218050,MONDO:0009027,"cramps, familial adolescent",
+BMGC_DS11647,BMG_DS040130,,,,,,,,,C1857569,,217700,MONDO:0009019,congenital hereditary endothelial dystrophy of cornea,
+BMGC_DS11648,BMG_DS040132,,CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS,,,,,DOID:0111620,corneal dystrophy-perceptive deafness syndrome,C1857572,,217400;610206,MONDO:0009015,corneal dystrophy-perceptive deafness syndrome,
+BMGC_DS11649,BMG_DS040133,,CORNEA PLANA 2,,,,,,,C1857574,,603288;217300,MONDO:0009014,cornea plana 2,
+BMGC_DS11650,BMG_DS040134,,"Convulsive Disorder, Familial, with Prenatal or Early Onset",,,,,,,C1857575,C565678,217200,MONDO:0009013,"convulsive disorder, familial, with prenatal or early onset",
+BMGC_DS11651,BMG_DS040135,,"Contractures, Congenital, Torticollis, and Malignant Hyperthermia",,,,,,,C1857576,C565679,217150,MONDO:0009012,multiple pterygium-malignant hyperthermia syndrome,
+BMGC_DS11652,BMG_DS040136,,ADAM COMPLEX,,,,,,,C1857577,,217100,,,
+BMGC_DS11653,BMG_DS040139,,Conotruncal cardiac defects,,,,,,,C1857586,C535464,217095,MONDO:0016581,conotruncal heart malformations,
+BMGC_DS11654,BMG_DS040140,,Orstavik Lindemann Solberg syndrome,,,,,,,C1857587,C537137,217085,MONDO:0009008,heart defect - tongue hamartoma - polysyndactyly syndrome,
+BMGC_DS11655,BMG_DS040141,,Amaurosis hypertrichosis,,,,,,,C1857588,C536604,204110,MONDO:0008766,amaurosis-hypertrichosis syndrome,
+BMGC_DS11656,BMG_DS040143,,Achromatopsia 2,,,,,DOID:0110007,achromatopsia 2,C1857618,C536128,216900,MONDO:0009003,achromatopsia 2,
+BMGC_DS11657,BMG_DS040144,,Coloboma of Macula and Skeletal Anomalies,,,,,,,C1857619,C565686,216800,MONDO:0009001,macular coloboma-cleft palate-hallux valgus syndrome,
+BMGC_DS11658,BMG_DS040145,,"COLLAGENOSIS, FAMILIAL REACTIVE PERFORATING",,,,,,,C1857624,,216700,MONDO:0009000,familial reactive perforating collagenosis,
+BMGC_DS11659,BMG_DS040147,721847002,COACH syndrome,,,,,DOID:0111589,COACH syndrome,C1857662,C536430,,MONDO:0100349,COACH syndrome,"Joubert syndrome with congenital hepatic fibrosis (disorder) | Joubert syndrome with hepatic defect | Joubert syndrome with congenital hepatic fibrosis | Cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis | COACH syndrome | Gentile syndrome | COACH (cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis) syndrome"
+BMGC_DS11660,BMG_DS040148,,Yunis Varon syndrome,,,,,DOID:0060589,Yunis-Varon syndrome,C1857663,C536719,216340,MONDO:0008995,Yunis-Varon syndrome,
+BMGC_DS11661,BMG_DS040149,,Combined Oxidative Phosphorylation Deficiency 4,,,,,DOID:0111494,combined oxidative phosphorylation deficiency 4,C1857682,C565690,610678,MONDO:0012534,combined oxidative phosphorylation defect type 4,
+BMGC_DS11662,BMG_DS040150,,"Telangiectasia, Hereditary Hemorrhagic, Type 4",,,,,,,C1857688,C565691,610655,MONDO:0012532,hereditary hemorrhagic telangiectasia type 4,
+BMGC_DS11663,BMG_DS040152,,"Anemia, Diamond-Blackfan, 3",,,,,DOID:0111887,Diamond-blackfan anemia 3,C1857719,C536355,610629,MONDO:0012529,Diamond-Blackfan anemia 3,
+BMGC_DS11664,BMG_DS040154,,Hereditary Angioedema Type III,Hereditary Angioedema Type III,,,,DOID:0080940,hereditary angioedema type III,C1857728,D056828,610618,MONDO:0012526,hereditary angioedema type 3,
+BMGC_DS11665,BMG_DS040155,,Leber Congenital Amaurosis 12,,,,,DOID:0110080,Leber congenital amaurosis 12,C1857743,C565697,610612,MONDO:0012525,Leber congenital amaurosis 12,
+BMGC_DS11666,BMG_DS040156,,"DEAFNESS, AUTOSOMAL RECESSIVE 59",,,,,,,C1857744,,610219;610220,MONDO:0012445,autosomal recessive nonsyndromic hearing loss 59,
+BMGC_DS11667,BMG_DS040157,,Neurodegeneration With Brain Iron Accumulation 2B,,,,,,,C1857747,C565699,610217,MONDO:0012444,neurodegeneration with brain iron accumulation 2B,
+BMGC_DS11668,BMG_DS040159,,"DEAFNESS, AUTOSOMAL RECESSIVE 66",,,,,,,C1857750,,610212;605755,MONDO:0012442,autosomal recessive nonsyndromic hearing loss 66,
+BMGC_DS11669,BMG_DS040160,,,,,,,,,C1857751,,610209,MONDO:0012441,"migraine with or without aura, susceptibility to, 11",
+BMGC_DS11670,BMG_DS040161,,,,,,,,,C1857752,,610208,MONDO:0012440,"migraine with or without aura, susceptibility to, 10",
+BMGC_DS11671,BMG_DS040162,,Alagille Syndrome 2,Alagille Syndrome,,,,,,C1857761,D016738,610205,MONDO:0012439,Alagille syndrome due to a NOTCH2 point mutation,
+BMGC_DS11672,BMG_DS040163,,"Olivopontocerebellar hypoplasia, fetal-onset",,,,,DOID:0060274,pontocerebellar hypoplasia type 5,C1857762,C537745,610204,MONDO:0012438,pontocerebellar hypoplasia type 5,
+BMGC_DS11673,BMG_DS040165,,"Cataract, Pulverulent, Juvenile-Onset",,,,,,,C1857768,C565703,610202,MONDO:0012437,cataract 21 multiple types,
+BMGC_DS11674,BMG_DS040166,,"Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism",,,,,,,C1857775,C565705,610199,MONDO:0012436,neonatal diabetes mellitus with congenital hypothyroidism,
+BMGC_DS11675,BMG_DS040167,,"3-@METHYLGLUTACONIC ACIDURIA, TYPE V",,,,,,,C1857776,,608977;610198,MONDO:0012435,3-methylglutaconic aciduria type 5,
+BMGC_DS11676,BMG_DS040168,,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 10",,,,,,,C1857777,C565707,610193,MONDO:0012434,arrhythmogenic right ventricular dysplasia 10,
+BMGC_DS11677,BMG_DS040169,,SENIOR-LOKEN SYNDROME 6,,,,,,,C1857779,,610142;610189,MONDO:0012433,Senior-Loken syndrome 6,
+BMGC_DS11678,BMG_DS040170,,JOUBERT SYNDROME 5,,,,,,,C1857780,,610142;610188,MONDO:0012432,Joubert syndrome 5,
+BMGC_DS11679,BMG_DS040171,,,,,,,,,C1857781,,610187,MONDO:0012431,diaphragmatic hernia 3,
+BMGC_DS11680,BMG_DS040173,,Immunodeficiency due to Defect in CD3-Zeta,,,,,DOID:0111942,immunodeficiency 25,C1857798,C565712,610163,MONDO:0012426,immunodeficiency 25,
+BMGC_DS11681,BMG_DS040174,,"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2",,,,,,,C1857800,,610158,MONDO:0012425,"corneal dystrophy, fuchs endothelial, 2",
+BMGC_DS11682,BMG_DS040175,715628009,MORM syndrome,,,,,,,C1857802,C536984,610156,MONDO:0012423,MORM syndrome,"Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome (disorder) | Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome | MORM syndrome | Mental retardation, truncal obesity, retinal dystrophy and micropenis syndrome | MORM (mental retardation, truncal obesity, retinal dystrophy, micropenis) syndrome"
+BMGC_DS11683,BMG_DS040177,,"Diabetes Mellitus, Insulin-Dependent, 19",,,,,,,C1857808,C565715,610155,MONDO:0012422,type 1 diabetes mellitus 19,
+BMGC_DS11684,BMG_DS040178,,"DEAFNESS, AUTOSOMAL RECESSIVE 44",,,,,,,C1857809,,103072;610154,MONDO:0012421,autosomal recessive nonsyndromic hearing loss 44,
+BMGC_DS11685,BMG_DS040179,,"DEAFNESS, AUTOSOMAL RECESSIVE 49",,,,,,,C1857811,,610153;610572,MONDO:0012420,autosomal recessive nonsyndromic hearing loss 49,
+BMGC_DS11686,BMG_DS040180,,"Macular Degeneration, Age-Related, 7",,,,,,,C1857813,C565718,610149,MONDO:0012419,age related macular degeneration 7,
+BMGC_DS11687,BMG_DS040181,,"DEAFNESS, AUTOSOMAL RECESSIVE 62",,,,,,,C1857820,,610143,MONDO:0012418,autosomal recessive nonsyndromic hearing loss 62,
+BMGC_DS11688,BMG_DS040182,,Leber Congenital Amaurosis 10,,,,,DOID:0110291,Leber congenital amaurosis 10,C1857821,C565720,611755,MONDO:0012723,Leber congenital amaurosis 10,
+BMGC_DS11689,BMG_DS040184,,"Heart-hand syndrome, Slovenian type",,,,,,,C1857829,C535852,610140,MONDO:0012417,"heart-hand syndrome, Slovenian type",
+BMGC_DS11690,BMG_DS040187,,Williams-Beuren Region Duplication Syndrome,,,,,,,C1857844,C565723,609757,MONDO:0012342,7q11.23 microduplication syndrome,
+BMGC_DS11691,BMG_DS040188,,,,,,,,,C1857845,,609755,MONDO:0012341,"celiac disease, susceptibility to, 3",
+BMGC_DS11692,BMG_DS040190,,,,,,,,,C1857847,,609753,MONDO:0012339,"celiac disease, susceptibility to, 4",
+BMGC_DS11693,BMG_DS040193,,"Cataract, Congenital Nuclear, Autosomal Recessive 2",,,,,,,C1857853,C565725,609741,MONDO:0012336,cataract 22 multiple types,
+BMGC_DS11694,BMG_DS040194,,Proopiomelanocortin Deficiency,,,,,,,C1857854,C565726,609734,MONDO:0012335,obesity due to pro-opiomelanocortin deficiency,
+BMGC_DS11695,BMG_DS040195,,"SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT",,,,,,,C1857855,,609727,MONDO:0012334,hereditary spastic paraplegia 29,
+BMGC_DS11696,BMG_DS040196,,"Alzheimer Disease, Familial Early-Onset, With Coexisting Amyloid And Prion Pathology",,,,,,,C1857933,C565728,605055,MONDO:0011513,"Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology",
+BMGC_DS11697,BMG_DS040197,703531009,Brooke-Spiegler syndrome,,,,,DOID:0050693,Brooke-Spiegler syndrome,C1857941,C536611,605041,MONDO:0011512,Brooke-Spiegler syndrome,Brooke-Spiegler syndrome | Spiegler-Brooke syndrome | Brooke-Spiegler syndrome (disorder)
+BMGC_DS11698,BMG_DS040201,,"Diabetes Mellitus, Congenital Autoimmune",,,,,,,C1857958,C565730,605026,MONDO:0011507,"diabetes mellitus, congenital autoimmune",
+BMGC_DS11699,BMG_DS040202,,"Hypobetalipoproteinemia, Familial, 2",,,,,,,C1857970,C565732,605019,MONDO:0011505,familial hypobetalipoproteinemia 2,
+BMGC_DS11700,BMG_DS040203,,MICROHYDRANENCEPHALY,,,,,,,C1857977,,605013;609449,MONDO:0011504,NDE1-related microhydranencephaly,
+BMGC_DS11701,BMG_DS040204,,WOLFRAM SYNDROME 2,,,,,,,C1858028,,611507;604928,MONDO:0011502,Wolfram syndrome 2,
+BMGC_DS11702,BMG_DS040206,,Becker Nevus Syndrome,,,,,,,C1858042,C565735,604919,MONDO:0011500,Becker nevus syndrome,
+BMGC_DS11703,BMG_DS040207,722065002,Okamoto syndrome,,,,,,,C1858043,,,,,Okamoto syndrome (disorder) | Okamoto syndrome
+BMGC_DS11704,BMG_DS040208,,,,,,,,,C1858050,,604906,MONDO:0011498,schizophrenia 9,
+BMGC_DS11705,BMG_DS040209,,NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS,,,,,,,C1858051,,604901,MONDO:0011497,hereditary North American Indian childhood cirrhosis,
+BMGC_DS11706,BMG_DS040210,,BARDET-BIEDL SYNDROME 6,,,,,,,C1858054,,604896;605231,MONDO:0011523,Bardet-Biedl syndrome 6,
+BMGC_DS11707,BMG_DS040211,,ASTHMA AND NASAL POLYPS,,,,,,,C1858067,,208550;604895,,,
+BMGC_DS11708,BMG_DS040212,,"Retinal Dystrophy, Early Onset Severe",,,,,,,C1858080,C565741,,,,
+BMGC_DS11709,BMG_DS040214,,"Stickler syndrome, type 2",,,,,,,C1858084,C537493,604841,MONDO:0011493,Stickler syndrome type 2,
+BMGC_DS11710,BMG_DS040216,,"Spastic paraplegia 12, autosomal dominant",,,,,,,C1858106,C537484,604805,MONDO:0011489,hereditary spastic paraplegia 12,
+BMGC_DS11711,BMG_DS040217,,"Microcephaly, Primary Autosomal Recessive, 3",,,,,,,C1858108,C565746,604804,MONDO:0011488,"microcephaly 3, primary, autosomal recessive",
+BMGC_DS11712,BMG_DS040218,,,,,,,,,C1858114,,604802,MONDO:0011487,Huntington disease-like 3,
+BMGC_DS11713,BMG_DS040219,,Caudate atrophy,,,,,,,C1858116,,MTHU004659,,,
+BMGC_DS11714,BMG_DS040220,,"Muscular Dystrophy, Congenital, 1B",,,,,,,C1858118,C565748,604801,MONDO:0011486,congenital muscular dystrophy 1B,
+BMGC_DS11715,BMG_DS040221,,"Ichthyosis, Nonlamellar and Nonerythrodermic, Congenital, Autosomal Recessive",,,,,,,C1858133,C565749,604777,MONDO:0011485,autosomal recessive congenital ichthyosis 5,
+BMGC_DS11716,BMG_DS040223,,"CARDIOMYOPATHY, DILATED, 1I",,,,,,,C1858154,,125660;604765,MONDO:0011482,dilated cardiomyopathy 1I,
+BMGC_DS11717,BMG_DS040224,,,,,,,,,C1858160,,604757,MONDO:0011481,craniosynostosis 2,
+BMGC_DS11718,BMG_DS040225,,"Deafness, Autosomal Dominant 20",,,,,,,C1858172,C565754,604717,MONDO:0011480,autosomal dominant nonsyndromic hearing loss 20,
+BMGC_DS11719,BMG_DS040229,,"Bare Lymphocyte Syndrome, Type I",,,,,,,C1858266,C565759,,MONDO:0011476,MHC class I deficiency,
+BMGC_DS11720,BMG_DS040230,,"Charcot-Marie-Tooth disease, Type 4B2",,,,,DOID:0110190,Charcot-Marie-Tooth disease type 4B2,C1858278,C535421,604563,MONDO:0011475,Charcot-Marie-Tooth disease type 4B2,
+BMGC_DS11721,BMG_DS040231,,"Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma",,,,,,,C1858279,C535422,,,,
+BMGC_DS11722,BMG_DS040233,,LEBER CONGENITAL AMAUROSIS 5,,,,,,,C1858301,,604537;611408,MONDO:0011473,Leber congenital amaurosis 5,
+BMGC_DS11723,BMG_DS040234,,Ectodermal Dysplasia-Skin Fragility Syndrome,,,,,,,C1858302,C536183,604536,MONDO:0011472,epidermolysis bullosa simplex due to plakophilin deficiency,
+BMGC_DS11724,BMG_DS040235,,INFLAMMATORY BOWEL DISEASE 3,,,,,,,C1858303,,604519,MONDO:0011471,inflammatory bowel disease 3,
+BMGC_DS11725,BMG_DS040237,,"Bile acid synthesis defect, congenital, 4",,,,,DOID:0111068,congenital bile acid synthesis defect 4,C1858328,C535444,214950,MONDO:0008967,congenital bile acid synthesis defect 4,
+BMGC_DS11726,BMG_DS040238,,"Neuropathy, hereditary motor and sensory, Okinawa type",,,,,,,C1858338,C535717,604484,MONDO:0011468,"hereditary motor and sensory neuropathy, Okinawa type",
+BMGC_DS11727,BMG_DS040240,,SPINOCEREBELLAR ATAXIA 11,,,,,DOID:0050961,spinocerebellar ataxia type 11,C1858351,,604432;611695,MONDO:0011464,spinocerebellar ataxia type 11,
+BMGC_DS11728,BMG_DS040242,,,,,,,,,C1858361,,604416,MONDO:0011462,pyogenic arthritis-pyoderma gangrenosum-acne syndrome,
+BMGC_DS11729,BMG_DS040243,,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 6",,,,,,,C1858378,C565775,604401,MONDO:0011460,arrhythmogenic right ventricular dysplasia 6,
+BMGC_DS11730,BMG_DS040244,,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 5",,,,,,,C1858379,C565776,604400,MONDO:0011459,arrhythmogenic right ventricular dysplasia 5,
+BMGC_DS11731,BMG_DS040245,,,,,,,,,C1858380,,614385,MONDO:0013725,"colorectal cancer, hereditary nonpolyposis, type 7",
+BMGC_DS11732,BMG_DS040246,,Leber Congenital Amaurosis 4,,,,,DOID:0110332,Leber congenital amaurosis 4,C1858386,C565778,604393,MONDO:0011458,Leber congenital amaurosis 4,
+BMGC_DS11733,BMG_DS040247,,,,,,,,,C1858391,,,MONDO:0011457,ataxia-telangiectasia-like disorder,
+BMGC_DS11734,BMG_DS040248,,NEPHRONOPHTHISIS 3,,,,,,,C1858392,,604387;608002,MONDO:0011456,nephronophthisis 3,
+BMGC_DS11735,BMG_DS040250,,Patent Ductus Arteriosus and Bicuspid Aortic Valve with Hand Anomalies,,,,,,,C1858420,C565782,604381,MONDO:0011454,patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome,
+BMGC_DS11736,BMG_DS040252,,"Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency",,,,,,,C1858424,C565784,,,,
+BMGC_DS11737,BMG_DS040253,,"Epilepsy, Partial, with Variable Foci",,,,,,,C1858477,C565785,,MONDO:0020310,familial focal epilepsy with variable foci,
+BMGC_DS11738,BMG_DS040255,,"Spastic paraplegia 11, autosomal recessive",,,,,,,C1858479,C537483,604360,MONDO:0011445,hereditary spastic paraplegia 11,
+BMGC_DS11739,BMG_DS040256,,,,,,,,,C1858493,,604352,MONDO:0011443,"febrile seizures, familial, 4",
+BMGC_DS11740,BMG_DS040257,,"Advanced Sleep-Phase Syndrome, Familial",,,,,,,C1858496,C565789,,MONDO:0015609,advanced sleep phase syndrome,
+BMGC_DS11741,BMG_DS040259,,Spinocerebellar Ataxia 12,,,,,,,C1858501,C565790,604326,MONDO:0011439,spinocerebellar ataxia type 12,
+BMGC_DS11742,BMG_DS040260,,"Acne, Adult",,,,,,,C1858506,C565791,604324,MONDO:0100486,adult acne,
+BMGC_DS11743,BMG_DS040261,,"MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE",,,,,DOID:0070291,primary autosomal recessive microcephaly 4,C1858516,,604321;609173,MONDO:0011437,"microcephaly 4, primary, autosomal recessive",
+BMGC_DS11744,BMG_DS040262,,SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1,,,,,,,C1858517,,604320,MONDO:0011436,autosomal recessive distal spinal muscular atrophy 1,
+BMGC_DS11745,BMG_DS040263,,"MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICAL MALFORMATIONS",,,,,DOID:0070293,primary autosomal recessive microcephaly 2 with or without cortical malformations,C1858535,,604317;613583,MONDO:0011435,"microcephaly 2, primary, autosomal recessive, with or without cortical malformations",
+BMGC_DS11746,BMG_DS040266,,Blepharophimosis with Facial and Genital Anomalies and Mental Retardation,,,,,,,C1858538,C565797,604314,MONDO:0011432,"blepharophimosis - intellectual disability syndrome, Verloes type",
+BMGC_DS11747,BMG_DS040267,,OVERLAP CONNECTIVE TISSUE DISEASE,,,,,,,C1858556,,604308,MONDO:0011431,MASS syndrome,
+BMGC_DS11748,BMG_DS040268,,"Rheumatoid Arthritis, Systemic Juvenile",,,,,,,C1858558,C565798,,MONDO:0019434,systemic-onset juvenile idiopathic arthritis,
+BMGC_DS11749,BMG_DS040269,,"ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3",,,,,,,C1858562,,604292;603273,MONDO:0011428,"ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3",
+BMGC_DS11750,BMG_DS040271,,"Cardiomyopathy, Dilated, 1h",,,,,,,C1858591,C536277,604288,MONDO:0011425,dilated cardiomyopathy 1H,
+BMGC_DS11751,BMG_DS040272,,Carney Triad,,,,,,,C1858592,C565803,604287,MONDO:0011424,Carney triad,
+BMGC_DS11752,BMG_DS040273,,"Limb-girdle muscular dystrophy, type 2E",,,,,,,C1858593,C535902,604286,MONDO:0011423,autosomal recessive limb-girdle muscular dystrophy type 2E,
+BMGC_DS11753,BMG_DS040274,,"Short Stature, Idiopathic, Autosomal",,,,,,,C1858656,C565805,604271,MONDO:0011420,short stature due to partial GHR deficiency,
+BMGC_DS11754,BMG_DS040277,,"HEMOCHROMATOSIS, TYPE 3",,,,,DOID:0111030,hemochromatosis type 3,C1858664,,604250;604720,MONDO:0011417,hemochromatosis type 3,
+BMGC_DS11755,BMG_DS040278,,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1",,,,,DOID:0111302,generalized epilepsy with febrile seizures plus 1,C1858672,,600235;604233,MONDO:0011416,"generalized epilepsy with febrile seizures plus, type 1",
+BMGC_DS11756,BMG_DS040279,,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2",,,,,DOID:0111294,generalized epilepsy with febrile seizures plus 2,C1858673,,604403;182389,MONDO:0011461,"generalized epilepsy with febrile seizures plus, type 2",
+BMGC_DS11757,BMG_DS040280,,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3",,,,,DOID:0111298,familial febrile seizures 8,C1858674,,137164;607681,,,
+BMGC_DS11758,BMG_DS040281,,Leber Congenital Amaurosis 3,,,,,DOID:0110331,Leber congenital amaurosis 3,C1858677,C565814,604232,MONDO:0011415,Leber congenital amaurosis 3,
+BMGC_DS11759,BMG_DS040282,,"CATARACT, AUTOSOMAL DOMINANT",,,,,,,C1858679,,604219,MONDO:0011413,cataract 9 multiple types,
+BMGC_DS11760,BMG_DS040283,702421006,Familial encephalopathy with neuroserpin inclusion bodies,,,,,DOID:0050831,familial encephalopathy with neuroserpin inclusion bodies,C1858680,C536841,604218,MONDO:0011412,familial encephalopathy with neuroserpin inclusion bodies,Familial encephalopathy with neuroserpin inclusion bodies | Familial encephalopathy with neuroserpin inclusion bodies (disorder) | Familial dementia with neuroserpin inclusion bodies
+BMGC_DS11761,BMG_DS040284,,Chudley-Mccullough syndrome,,,,,,,C1858695,C535459,604213,MONDO:0011411,Chudley-McCullough syndrome,
+BMGC_DS11762,BMG_DS040287,,"Spastic paraplegia 10, autosomal dominant",,,,,,,C1858712,C537482,604187,MONDO:0011408,hereditary spastic paraplegia 10,
+BMGC_DS11763,BMG_DS040288,,"Facial paresis, hereditary, congenital",,,,,,,C1858717,C536386,604185,MONDO:0011407,"facial paresis, hereditary congenital, 2",
+BMGC_DS11764,BMG_DS040289,,Poikiloderma with Neutropenia,,,,,DOID:0060551,poikiloderma with neutropenia,C1858723,C565820,604173,MONDO:0011405,poikiloderma with neutropenia,
+BMGC_DS11765,BMG_DS040291,,,,,,,,,C1858725,,604169,MONDO:0011403,left ventricular noncompaction 1,
+BMGC_DS11766,BMG_DS040292,,"Congenital Cataracts, Facial Dysmorphism, And Neuropathy",,,,,,,C1858726,C565822,604168,MONDO:0011402,congenital cataracts-facial dysmorphism-neuropathy syndrome,
+BMGC_DS11767,BMG_DS040294,,"Cardiomyopathy, Dilated, 1g",,,,,,,C1858763,C565824,604145,MONDO:0011400,dilated cardiomyopathy 1G,
+BMGC_DS11768,BMG_DS040295,,"Cerebellar Ataxia, Deafness, and Narcolepsy",,,,,,,C1858804,C565825,,,,
+BMGC_DS11769,BMG_DS040296,,"Vohwinkel Syndrome, Variant Form",,,,,,,C1858805,C565826,604117,MONDO:0011396,loricrin keratoderma,
+BMGC_DS11770,BMG_DS040297,,Cone-Rod Dystrophy 3,,,,,DOID:0111013,cone-rod dystrophy 3,C1858806,C565827,604116,MONDO:0011395,cone-rod dystrophy 3,
+BMGC_DS11771,BMG_DS040298,,"DEAFNESS, AUTOSOMAL RECESSIVE 20",,,,,,,C1858840,,604060,MONDO:0011392,autosomal recessive nonsyndromic hearing loss 20,
+BMGC_DS11772,BMG_DS040299,,,,,,,DOID:0080315;DOID:0080316,megalencephalic leukoencephalopathy with subcortical cysts 1 | megalencephalic leukoencephalopathy with subcortical cysts,C1858854,,,MONDO:0011391,megalencephalic leukoencephalopathy with subcortical cysts,
+BMGC_DS11773,BMG_DS040300,,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2,,,,,,,C1858915,,603652;603965,MONDO:0011390,focal segmental glomerulosclerosis 2,
+BMGC_DS11774,BMG_DS040301,,"DEAFNESS, AUTOSOMAL DOMINANT 16",,,,,,,C1858916,,603964,MONDO:0011389,autosomal dominant nonsyndromic hearing loss 16,
+BMGC_DS11775,BMG_DS040304,,"Autoimmune Lymphoproliferative Syndrome, Type IIA",,,,,DOID:0110115,autoimmune lymphoproliferative syndrome type 2A,C1858968,C565833,603909,MONDO:0011383,autoimmune lymphoproliferative syndrome type 2A,
+BMGC_DS11776,BMG_DS040305,,"Beta Thalassemia, Dominant Inclusion Body Type",,,,,,,C1858990,C565834,603902,MONDO:0011381,dominant beta-thalassemia,
+BMGC_DS11777,BMG_DS040306,,Childhood Ataxia with Central Nervous System Hypomyelinization,Leukoencephalopathies,,,,,,C1858991,D056784,,MONDO:0800448,leukoencephalopathy with vanishing white matter,
+BMGC_DS11778,BMG_DS040307,,CCHS WITH HIRSCHSPRUNG DISEASE,,,,,,,C1859049,,209880;603851,MONDO:0020493,Haddad syndrome,
+BMGC_DS11779,BMG_DS040308,,LONG QT SYNDROME 3,,,,,,,C1859062,,600163;603830,MONDO:0011377,long QT syndrome 3,
+BMGC_DS11780,BMG_DS040310,,"Cleidocranial Dysplasia, Recessive Form",,,,,,,C1859080,C565843,216330,MONDO:0008994,"cleidocranial dysplasia, recessive form",
+BMGC_DS11781,BMG_DS040311,,"Cleft Palate, Deafness, and Oligodontia",,,,,,,C1859081,C565844,216300,MONDO:0008993,cleft palate-stapes fixation-oligodontia syndrome,
+BMGC_DS11782,BMG_DS040312,,Verloove-Vanhorick Brubakk syndrome,,,,,,,C1859082,C536541,215850,MONDO:0008991,Verloove Vanhorick-Brubakk syndrome,
+BMGC_DS11783,BMG_DS040313,,Novak syndrome,,,,,,,C1859083,C537851,215800,MONDO:0008990,"cleft larynx, posterior",
+BMGC_DS11784,BMG_DS040314,,Citrulline transport defect,,,,,,,C1859084,C536207,215720,MONDO:0008989,citrulline transport defect,
+BMGC_DS11785,BMG_DS040315,,"COPPER TOXICOSIS, IDIOPATHIC",,,,,,,C1859088,,215600,,,
+BMGC_DS11786,BMG_DS040316,,Circumvallate Placenta Syndrome,,,,,,,C1859089,C565847,215550,MONDO:0008986,circumvallate placenta syndrome,
+BMGC_DS11787,BMG_DS040318,,Choroid plexus calcification with mental retardation,,,,,,,C1859092,C535357,215480,MONDO:0008981,infantile choroidocerebral calcification syndrome,
+BMGC_DS11788,BMG_DS040319,,"Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism",,,,,DOID:0111265,Boucher-Neuhauser syndrome,C1859093,C565850,215470,MONDO:0008980,ataxia-hypogonadism-choroidal dystrophy syndrome,
+BMGC_DS11789,BMG_DS040320,,"Chorea, Benign Familial",,,,,,,C1859098,C565851,215450,MONDO:0008979,"chorea, benign familial",
+BMGC_DS11790,BMG_DS040322,,"Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome",,,,,,,C1859104,C565852,215250,MONDO:0008976,"chondroitin-6-sulfaturia, defective cellular immunity, nephrotic syndrome",
+BMGC_DS11791,BMG_DS040324,,"RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1",,,,,,,C1859133,,215100;601757,MONDO:0008972,rhizomelic chondrodysplasia punctata type 1,
+BMGC_DS11792,BMG_DS040325,,Chondrodysplasia Calcificans Metaphysealis,,,,,,,C1859147,C565855,215050,MONDO:0008971,chondrodysplasia calcificans Metaphysealis,
+BMGC_DS11793,BMG_DS040326,,"Chondrodysplasia, blomstrand type",,,,,DOID:0060387,chondrodysplasia Blomstrand type,C1859148,C537914,215045,MONDO:0008970,chondrodysplasia Blomstrand type,
+BMGC_DS11794,BMG_DS040329,,"GRISCELLI SYNDROME, TYPE 1",,,,,DOID:0060832,Griscelli syndrome type 1,C1859194,,214450;160777,MONDO:0008962,Griscelli syndrome type 1,
+BMGC_DS11795,BMG_DS040330,,"Charcot-Marie-Tooth disease, Type 4A",,,,,DOID:0110185,Charcot-Marie-Tooth disease type 4A,C1859198,C535419,214400,MONDO:0008961,Charcot-Marie-Tooth disease type 4A,
+BMGC_DS11796,BMG_DS040331,,Klippel Feil syndrome recessive type,,,,,,,C1859209,C536888,214300,MONDO:0008958,"Klippel-Feil syndrome 2, autosomal recessive",
+BMGC_DS11797,BMG_DS040333,,Cerebrofaciothoracic Dysplasia,,,,,,,C1859252,C565862,,,,
+BMGC_DS11798,BMG_DS040335,,Pelizaeus-Merzbacher like brain sclerosis,,,,,,,C1859258,C536318,213900,MONDO:0008950,cerebral sclerosis similar to Pelizaeus-Merzbacher disease,
+BMGC_DS11799,BMG_DS040337,,"Cerebral Angiopathy, Dysphoric",,,,,,,C1859283,C565864,213500,MONDO:0008946,"cerebral angiopathy, dysphoric",
+BMGC_DS11800,BMG_DS040338,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2",,,,,DOID:0080061,autosomal recessive spinocerebellar ataxia 2,C1859298,,613036;213200,MONDO:0008943,autosomal recessive spinocerebellar ataxia 2,
+BMGC_DS11801,BMG_DS040339,,Cerebellar Vermis Aplasia with Associated Features suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome,,,,,,,C1859300,C565867,213010,MONDO:0008941,hepatic fibrosis-renal cysts-intellectual disability syndrome,
+BMGC_DS11802,BMG_DS040340,,"Cerebellar Ataxia, Benign, with Thermoanalgesia",,,,,,,C1859303,C565868,212890,MONDO:0008937,"cerebellar ataxia, benign, with thermoanalgesia",
+BMGC_DS11803,BMG_DS040341,,Cerebellar Ataxia and Neurosensory Deafness,,,,,,,C1859304,C565869,212850,MONDO:0008936,cerebellar ataxia and neurosensory deafness,
+BMGC_DS11804,BMG_DS040342,,Cerebellar Ataxia and Hypogonadotropic Hypogonadism,,,,,DOID:0111587,Gordon Holmes syndrome,C1859305,C565870,212840,MONDO:0008935,cerebellar ataxia-hypogonadism syndrome,
+BMGC_DS11805,BMG_DS040344,,Cephalin Lipidosis,,,,,,,C1859307,C565872,212800,MONDO:0008933,cephalin lipidosis,
+BMGC_DS11806,BMG_DS040345,,PREMATURE CENTROMERE DIVISION,,,,,,,C1859308,,212790,MONDO:0008932,premature centromere division,
+BMGC_DS11807,BMG_DS040346,,Syndactyly Cenani Lenz type,,,,,,,C1859309,C538150,212780,MONDO:0008931,Cenani-Lenz syndactyly syndrome,
+BMGC_DS11808,BMG_DS040347,,,,,,,,,C1859310,,212750,MONDO:0008930,"celiac disease, susceptibility to, 1",
+BMGC_DS11809,BMG_DS040348,,"Microphthalmia, Isolated, with Cataract 2",,,,,,,C1859311,C565876,,,,
+BMGC_DS11810,BMG_DS040350,,Cataract and congenital ichthyosis,,,,,,,C1859315,C538281,212400,MONDO:0008924,congenital cataract-ichthyosis syndrome,
+BMGC_DS11811,BMG_DS040351,,CATARACT-ALOPECIA-SCLERODACTYLY SYNDROME,,,,,DOID:0111245,palmoplantar keratoderma and congenital alopecia 2,C1859316,,212360,MONDO:0008923,autosomal recessive palmoplantar keratoderma and congenital alopecia,
+BMGC_DS11812,BMG_DS040352,,Cataract and cardiomyopathy,,,,,DOID:0080132,Sengers syndrome,C1859317,C538280,212350,MONDO:0008922,Sengers syndrome,
+BMGC_DS11813,BMG_DS040353,,Myopathic carnitine deficiency,,,,,,,C1859318,C536100,212160,MONDO:0008920,"carnitine deficiency, myopathic",
+BMGC_DS11814,BMG_DS040355,,Cardiomyopathy Associated With Myopathy And Sudden Death,,,,,,,C1859328,C565881,212130,MONDO:0008916,cardiomyopathy associated with myopathy and sudden death,
+BMGC_DS11815,BMG_DS040356,,Cardioauditory syndrome of Sanchez Cascos,,,,,,,C1859329,C535577,212100,MONDO:0008914,cardioauditory syndrome of Sanchez Cascos,
+BMGC_DS11816,BMG_DS040358,,Cardiac Septal Defects with Coarctation of the Aorta,,,,,,,C1859331,C565883,212090,MONDO:0008912,cardiac septal defects with coarctation of the aorta,
+BMGC_DS11817,BMG_DS040359,,"Cardiac Lipidosis, Familial",,,,,,,C1859332,C565884,212080,MONDO:0008911,"cardiac lipidosis, familial",
+BMGC_DS11818,BMG_DS040360,,"Candidiasis, Familial, 2",,,,,,,C1859353,C537979,212050,MONDO:0008905,predisposition to invasive fungal disease due to CARD9 deficiency,
+BMGC_DS11819,BMG_DS040361,,Camptomelic syndrome long limb type,,,,,,,C1859354,C537977,211990,MONDO:0008904,"camptomelic syndrome, long-limb type",
+BMGC_DS11820,BMG_DS040363,719946008,Tel Hashomer camptodactyly syndrome,,,,,,,C1859356,C536953,211960,MONDO:0008901,Tel Hashomer camptodactyly syndrome,Tel Hashomer camptodactyly syndrome (disorder) | Tel Hashomer camptodactyly syndrome
+BMGC_DS11821,BMG_DS040365,720599002,Campomelia Cumming type,,,,,,,C1859371,C537966,211890,MONDO:0008896,"campomelia, Cumming type",Campomelia Cumming type (disorder) | Campomelia Cumming type | Cumming syndrome
+BMGC_DS11822,BMG_DS040366,,Calcification of Joints and Arteries,,,,,,,C1859372,C565891,211800,MONDO:0008895,hereditary arterial and articular multiple calcification syndrome,
+BMGC_DS11823,BMG_DS040368,,"Brachydactyly, Type A2, With Microcephaly",,,,,,,C1859393,C565894,211369,MONDO:0008883,"brachydactyly, type A2, with microcephaly",
+BMGC_DS11824,BMG_DS040371,711153001,Bowen-Conradi syndrome,,,,,DOID:0050684,Bowen-Conradi syndrome,C1859405,C537081,211180,MONDO:0008879,Bowen-Conradi syndrome,Bowen-Conradi syndrome (disorder) | Bowen-Conradi syndrome | Hutterite syndrome | Bowen Hutterite syndrome | Bowen-Conradi Hutterite syndrome
+BMGC_DS11825,BMG_DS040373,,"Blepharophimosis with ptosis, syndactyly, and short stature",,,,,,,C1859432,C536235,210745,MONDO:0008875,blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome,
+BMGC_DS11826,BMG_DS040375,,"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I",,,,,,,C1859452,,210710;601428,MONDO:0008871,microcephalic osteodysplastic primordial dwarfism type I,
+BMGC_DS11827,BMG_DS040376,,Bird headed dwarfism Montreal type,,,,,,,C1859468,C535448,210700,MONDO:0008870,"bird headed-dwarfism, Montreal type",
+BMGC_DS11828,BMG_DS040377,,BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY,,,,,DOID:0050664,Bietti crystalline corneoretinal dystrophy,C1859486,,210370;608614,MONDO:0008865,Bietti crystalline corneoretinal dystrophy,
+BMGC_DS11829,BMG_DS040378,,Biemond syndrome II,,,,,,,C1859487,C565902,210350,MONDO:0008864,Biemond syndrome type 2,
+BMGC_DS11830,BMG_DS040379,,3-methylcrotonyl CoA carboxylase 2 deficiency,,,,,DOID:0080580,3-methylcrotonyl-CoA carboxylase 2 deficiency,C1859499,C535309,210210,MONDO:0008862,3-methylcrotonyl-CoA carboxylase 2 deficiency,
+BMGC_DS11831,BMG_DS040380,,"Beta-Aminoisobutyric Acid, Urinary Excretion of",,,,,,,C1859518,C565904,210100,MONDO:0008860,"beta-aminoisobutyric acid, urinary excretion of",
+BMGC_DS11832,BMG_DS040381,,"Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification",,,,,,,C1859519,C565905,210050,MONDO:0008859,"berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification",
+BMGC_DS11833,BMG_DS040382,717859007,Beemer Ertbruggen syndrome,,,,,,,C1859526,C537668,209970,MONDO:0008857,Beemer-Ertbruggen syndrome,"Hydrocephalus, cardiac malformation, dense bone syndrome (disorder) | Hydrocephalus, cardiac malformation, dense bone syndrome | Beemer Ertbruggen syndrome | Beemer lethal malformation syndrome"
+BMGC_DS11834,BMG_DS040387,,"Bare Lymphocyte Syndrome, Type II, Complementation Group B",,,,,,,C1859535,C565910,620815,MONDO:0971013,MHC class II deficiency 2,
+BMGC_DS11835,BMG_DS040388,,"Bare Lymphocyte Syndrome, Type II, Complementation Group C",,,,,,,C1859536,C565910,620816,MONDO:0971014,MHC class II deficiency 3,
+BMGC_DS11836,BMG_DS040389,,"Bare Lymphocyte Syndrome, Type II, Complementation Group D",,,,,,,C1859537,C565910,620817,MONDO:0971015,MHC class II deficiency 4,
+BMGC_DS11837,BMG_DS040390,,"Bare Lymphocyte Syndrome, Type II, Complementation Group E",,,,,,,C1859538,C565910,620818,MONDO:0971016,MHC class II deficiency 5,
+BMGC_DS11838,BMG_DS040391,,Bardet-Biedl syndrome 3,,,,,DOID:0110125,Bardet-Biedl syndrome 3,C1859564,C537911,600151,MONDO:0010832,Bardet-Biedl syndrome 3,
+BMGC_DS11839,BMG_DS040392,,BARDET-BIEDL SYNDROME 7,,,,,,,C1859565,,615984;607590,MONDO:0014435,Bardet-Biedl syndrome 7,
+BMGC_DS11840,BMG_DS040393,,BARDET-BIEDL SYNDROME 8,,,,,,,C1859566,,608132;615985,MONDO:0014436,Bardet-Biedl syndrome 8,
+BMGC_DS11841,BMG_DS040394,,BARDET-BIEDL SYNDROME 9,,,,,,,C1859567,,607968;615986,MONDO:0014437,Bardet-Biedl syndrome 9,
+BMGC_DS11842,BMG_DS040395,,BARDET-BIEDL SYNDROME 10,,,,,,,C1859568,,610148;615987,MONDO:0014438,Bardet-Biedl syndrome 10,
+BMGC_DS11843,BMG_DS040396,,BARDET-BIEDL SYNDROME 11,,,,,,,C1859569,,602290;615988,MONDO:0014439,Bardet-Biedl syndrome 11,
+BMGC_DS11844,BMG_DS040397,,BARDET-BIEDL SYNDROME 12,,,,,,,C1859570,,615989;610683,MONDO:0014440,Bardet-Biedl syndrome 12,
+BMGC_DS11845,BMG_DS040398,,"Aural Atresia, Multiple Congenital Anomalies, and Mental Retardation",,,,,,,C1859591,C565923,209770,MONDO:0008850,Cooper-Jabs syndrome,
+BMGC_DS11846,BMG_DS040399,,ATRICHIA WITH PAPULAR LESIONS,,,,,,,C1859592,,209500;602302,MONDO:0008847,atrichia with papular lesions,
+BMGC_DS11847,BMG_DS040400,,Atonic-Astatic Syndrome of Foerster,,,,,,,C1859594,C565926,209100,MONDO:0008845,atonic-astatic syndrome of Foerster,
+BMGC_DS11848,BMG_DS040401,,"Athrombia, Essential",,,,,,,C1859595,C565927,209050,MONDO:0008844,"Athrombia, essential",
+BMGC_DS11849,BMG_DS040402,,"Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease",,,,,,,C1859596,C565928,209010,MONDO:0008843,atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome,
+BMGC_DS11850,BMG_DS040403,,"ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA",,,,,DOID:0050754,ataxia with oculomotor apraxia type 1,C1859598,,208920;606350,MONDO:0008842,"ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia",
+BMGC_DS11851,BMG_DS040405,,"Ataxia, Deafness, and Cardiomyopathy",,,,,,,C1859645,C565932,208750,MONDO:0008837,"ataxia, deafness, and cardiomyopathy",
+BMGC_DS11852,BMG_DS040406,,Ataxia with Myoclonic Epilepsy and Presenile Dementia,,,,,,,C1859646,C565933,208700,MONDO:0008836,ataxia with myoclonic epilepsy and presenile dementia,
+BMGC_DS11853,BMG_DS040407,,"Asthma, Short Stature, and Elevated IgA",,,,,,,C1859647,C565934,208600,MONDO:0008835,"asthma, short stature, and elevated IgA",
+BMGC_DS11854,BMG_DS040408,,"Asthma, Nasal Polyps, And Aspirin Intolerance",,,,,DOID:0111579,"asthma, nasal polyps, and aspirin intolerance",C1859648,C565935,208550,MONDO:0008834,"asthma, nasal polyps, and aspirin intolerance",
+BMGC_DS11855,BMG_DS040409,,CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME,,,,,DOID:0090127,camptodactyly-arthropathy-coxa vara-pericarditis syndrome,C1859690,,208250;604283,MONDO:0008828,camptodactyly-arthropathy-coxa vara-pericarditis syndrome,
+BMGC_DS11856,BMG_DS040411,,Kuskokwim disease,,,,,,,C1859709,C538124,208200,MONDO:0015241,arthrogryposis-like syndrome,
+BMGC_DS11857,BMG_DS040412,726620005,Johnston Aarons Schelley syndrome,,,,,,,C1859710,C535883,208158,MONDO:0008826,"arthrogryposis-hyperkeratosis syndrome, lethal form",Arthrogryposis hyperkeratosis syndrome lethal form (disorder) | Arthrogryposis hyperkeratosis syndrome lethal form | Johnston Aarons Schelley syndrome
+BMGC_DS11858,BMG_DS040413,,Arthrogryposis multiplex congenita whistling face,,,,,,,C1859711,C538401,208155,MONDO:0008825,arthrogryposis multiplex congenita-whistling face syndrome,
+BMGC_DS11859,BMG_DS040414,,Arthrogryposis multiplex congenita neurogenic type,,,,,DOID:0090124,neurogenic-type arthrogryposis multiplex congenita-2,C1859721,C536614,,,,
+BMGC_DS11860,BMG_DS040415,,"Arthrogryposis, renal dysfunction, and cholestasis 1",,,,,,,C1859722,C535382,208085,MONDO:0008822,"arthrogryposis, renal dysfunction, and cholestasis 1",
+BMGC_DS11861,BMG_DS040418,,"Arteriosclerosis, Severe Juvenile",,,,,,,C1859725,C565941,208060,MONDO:0008819,"arteriosclerosis, severe juvenile",
+BMGC_DS11862,BMG_DS040419,,ARTERIAL TORTUOSITY SYNDROME,,,,,,,C1859726,,208050;606145,MONDO:0008818,arterial tortuosity syndrome,
+BMGC_DS11863,BMG_DS040420,,Arterial calcification of infancy,,,,,DOID:0050644,arterial calcification of infancy,C1859727,C537440,,MONDO:0018870,arterial calcification of infancy,
+BMGC_DS11864,BMG_DS040421,,"Coronary Sclerosis, Medial, of Infancy",,,,,,,C1859728,C565944,,,,
+BMGC_DS11865,BMG_DS040422,,"Aplasia of Extensor Muscles of Fingers, Unilateral, with Generalized Polyneuropathy",,,,,,,C1859752,C565945,207740,MONDO:0008809,polyneuropathy-hand defect syndrome,
+BMGC_DS11866,BMG_DS040423,,Aplasia cutis congenita intestinal lymphangiectasia,,,,,,,C1859753,C537788,207731,MONDO:0008808,aplasia cutis congenita-intestinal lymphangiectasia syndrome,
+BMGC_DS11867,BMG_DS040425,,"Antithrombin, Familial Hemorrhagic Diathesis due to",,,,,,,C1859761,C565947,207300,MONDO:0008802,"antithrombin, familial hemorrhagic diathesis due to",
+BMGC_DS11868,BMG_DS040426,,,,,,,,,C1859762,,207000,MONDO:0008801,anosmia for isobutyric acid,
+BMGC_DS11869,BMG_DS040428,,"Microphthalmia, Syndromic 3",,,,,DOID:0111801,syndromic microphthalmia 3,C1859773,C565948,206900,MONDO:0008799,anophthalmia/microphthalmia-esophageal atresia syndrome,
+BMGC_DS11870,BMG_DS040429,,Optic Nerve Hypoplasia and Abnormalities of the Central Nervous System,,,,,,,C1859774,C565949,,,,
+BMGC_DS11871,BMG_DS040430,,Aniridia renal agenesis psychomotor retardation,,,,,,,C1859782,C000632444,206750,MONDO:0008796,aniridia-renal agenesis-psychomotor retardation syndrome,
+BMGC_DS11872,BMG_DS040431,,"Angiomatosis, diffuse corticomeningeal, of Divry and Van Bogaert",,,,,,,C1859783,C536367,206570,MONDO:0008793,"angiomatosis, diffuse Corticomeningeal, of Divry and van Bogaert",
+BMGC_DS11873,BMG_DS040432,,"Angiolipomatosis, Familial",,,,,,,C1859784,C565951,206550,MONDO:0008792,familial angiolipomatosis,
+BMGC_DS11874,BMG_DS040433,,"Anemia, Nonspherocytic Hemolytic, possibly due to Defect in Porphyrin Metabolism",,,,,,,C1859785,C565952,206400,MONDO:0008790,"anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism",
+BMGC_DS11875,BMG_DS040434,,"Anemia, Nonspherocytic Hemolytic, associated with Abnormality of Red Cell Membrane",,,,,,,C1859786,C565953,206300,MONDO:0008789,"anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane",
+BMGC_DS11876,BMG_DS040436,,Amyotrophic Lateral Sclerosis With Polyglucosan Bodies,,,,,,,C1859805,C565955,205250,MONDO:0008782,amyotrophic lateral sclerosis with polyglucosan bodies,
+BMGC_DS11877,BMG_DS040437,,"Amyotrophic Lateral Sclerosis, Juvenile, with Dementia",,,,,,,C1859806,C565956,205200,MONDO:0008781,juvenile amyotrophic lateral sclerosis with dementia,
+BMGC_DS11878,BMG_DS040438,,"Amyotrophic Lateral Sclerosis 2, Juvenile",,,,,,,C1859807,C565957,205100,MONDO:0008780,"amyotrophic lateral sclerosis type 2, juvenile",
+BMGC_DS11879,BMG_DS040439,,"Amyloidosis of Gingiva and Conjunctiva, with Mental Retardation",,,,,,,C1859815,C565958,204850,MONDO:0008776,"amyloidosis of gingiva and conjunctiva, with intellectual disability",
+BMGC_DS11880,BMG_DS040440,,"Amobarbital, Deficient N-Hydroxylation of",,,,,,,C1859816,C565959,204800,MONDO:0008775,"Amobarbital, deficient N-hydroxylation of",
+BMGC_DS11881,BMG_DS040441,782918002,2-aminoadipic 2-oxoadipic aciduria,,,,,,,C1859817,,204750;245130,MONDO:0008774,2-aminoadipic 2-oxoadipic aciduria,2-aminoadipic 2-oxoadipic aciduria (disorder) | Alpha-aminoadipic aciduria | 2-aminoadipic 2-oxoadipic aciduria
+BMGC_DS11882,BMG_DS040442,,"Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis",,,,,,,C1859818,C565960,204730,MONDO:0008773,"amino aciduria with mental deficiency, dwarfism, muscular dystrophy, osteoporosis, and acidosis",
+BMGC_DS11883,BMG_DS040443,,"Amaurosis congenita of Leber, type 2",,,,,,,C1859844,C536601,204100,MONDO:0008765,Leber congenital amaurosis 2,
+BMGC_DS11884,BMG_DS040444,,Alpha-2-Deficient Collagen Disease,,,,,,,C1859850,C565963,203760,MONDO:0008761,obsolete alpha-2-deficient collagen disease,
+BMGC_DS11885,BMG_DS040445,,,,,,,,,C1859877,,203655,MONDO:0008757,alopecia universalis congenita,
+BMGC_DS11886,BMG_DS040446,,Alopecia-Mental Retardation Syndrome 1,,,,,,,C1859878,C565965,203650,MONDO:0021035,alopecia-intellectual disability syndrome 1,
+BMGC_DS11887,BMG_DS040447,,Microcephaly albinism digital anomalies syndrome,,,,,,,C1859910,C537322,203340,MONDO:0008750,microcephaly-albinism-digital anomalies syndrome,
+BMGC_DS11888,BMG_DS040448,,Coloboma of Alar-nasal cartilages with telecanthus,,,,,,,C1859964,C535967,203000,MONDO:0008744,alar cartilages hypoplasia-coloboma-telecanthus syndrome,
+BMGC_DS11889,BMG_DS040450,,"Neutropenia, Severe Congenital, Autosomal Dominant 1",,,,,,,C1859966,C565969,202700,MONDO:0042490,"neutropenia, severe congenital, 1, autosomal dominant",
+BMGC_DS11890,BMG_DS040452,,,,,,,,,C1859969,,202600,MONDO:0008739,agenesis of cerebral white matter,
+BMGC_DS11891,BMG_DS040453,,"Hypodysfibrinogenemia, Congenital",,,,,,,C1859970,C565970,,MONDO:0016638,familial hypodysfibrinogenemia,
+BMGC_DS11892,BMG_DS040454,,Adrenocortical Unresponsiveness To Acth With Postreceptor Defect,,,,,,,C1859971,C565971,202355,MONDO:0008735,adrenocortical unresponsiveness to ACTH with postreceptor defect,
+BMGC_DS11893,BMG_DS040455,,,,,,,,,C1859972,,202300,MONDO:0008734,"adrenocortical carcinoma, hereditary",
+BMGC_DS11894,BMG_DS040456,,"Adrenal Hypoplasia, Cytomegalic Type",,,,,,,C1859977,C564543,202155,MONDO:0008732,"adrenal hypoplasia, cytomegalic type",
+BMGC_DS11895,BMG_DS040457,,"Adrenal Hypoplasia, Congenital, With Absent Pituitary Luteinizing Hormone",,,,,,,C1859978,C565976,202150,MONDO:0008731,familial adrenal hypoplasia with absent pituitary luteinizing hormone,
+BMGC_DS11896,BMG_DS040458,,"Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency",,,,,,,C1859995,C565977,,,,
+BMGC_DS11897,BMG_DS040459,,Antley-Bixler Syndrome with Disordered Steroidogenesis,Antley-Bixler Syndrome Phenotype,,,,,,C1860042,D054882,613571,MONDO:0013310,congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency,
+BMGC_DS11898,BMG_DS040460,,Severe short-limb dwarfism,,,,,,,C1860105,,MTHU014753,,,
+BMGC_DS11899,BMG_DS040461,,Acrofrontofacionasal dysostosis syndrome,,,,,DOID:0060226,acrofrontofacionasal dysostosis,C1860118,C538186,,MONDO:0008715,acrofrontofacionasal dysostosis,
+BMGC_DS11900,BMG_DS040462,720430002,Acrofacial dysostosis Rodriguez type,,,,,DOID:0060383,acrofacial dysostosis Rodriguez type,C1860119,C538183,201170,MONDO:0008714,acrofacial dysostosis Rodriguez type,Acrofacial dysostosis Rodriguez type (disorder) | Acrofacial dysostosis Rodriguez type
+BMGC_DS11901,BMG_DS040464,,Elejalde Disease,,,,,,,C1860157,C536203,256710,MONDO:0009742,neuroectodermal melanolysosomal disease,
+BMGC_DS11902,BMG_DS040465,720414005,Acrorenal mandibular syndrome,,,,,,,C1860166,C535665,200980,MONDO:0008707,acro-renal-mandibular syndrome,Acrorenal mandibular syndrome (disorder) | Acrorenal mandibular syndrome | Split hand and split foot with mandibular hypoplasia syndrome | Acro-renal-mandibular syndrome
+BMGC_DS11903,BMG_DS040466,722280000,Ackerman syndrome,,,,,,,C1860167,C538170,200970,MONDO:0008706,Ackerman syndrome,Ackerman syndrome (disorder) | Ackerman syndrome
+BMGC_DS11904,BMG_DS040467,,Short-Limb Skeletal Dysplasia with Severe Combined Immunodeficiency,,,,,,,C1860168,C565984,200900,MONDO:0008704,short-limb skeletal dysplasia with severe combined immunodeficiency,
+BMGC_DS11905,BMG_DS040468,,Achalasia microcephaly,,,,,DOID:0050796,achalasia microcephaly syndrome,C1860212,C536010,200450,MONDO:0008699,achalasia microcephaly syndrome,
+BMGC_DS11906,BMG_DS040469,,"Achalasia, familial esophageal",,,,,,,C1860213,C536011,200400,MONDO:0100457,"achalasia, familial esophageal",
+BMGC_DS11907,BMG_DS040470,,Acanthosis nigricans muscle cramps acral enlargement,,,,,,,C1860215,C536000,200170,MONDO:0008696,acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome,
+BMGC_DS11908,BMG_DS040471,,ABLEPHARON-MACROSTOMIA SYNDROME,,,,,DOID:0060550,ablepharon macrostomia syndrome,C1860224,,607556;200110,MONDO:0008693,ablepharon macrostomia syndrome,
+BMGC_DS11909,BMG_DS040472,,,,,,,,,C1860228,,194470,MONDO:0008691,"zinc, elevated plasma",
+BMGC_DS11910,BMG_DS040474,,,,,,,,,C1860237,,194320,MONDO:0008687,Woronets trait,
+BMGC_DS11911,BMG_DS040475,,,,,,,,,C1860238,,194300,MONDO:0020717,autosomal dominant wooly hair,
+BMGC_DS11912,BMG_DS040476,,Wilms Tumor 3,,,,,,,C1860265,C565991,194090,MONDO:0008683,Wilms tumor 3,
+BMGC_DS11913,BMG_DS040477,,"Whispering dysphonia, hereditary",,,,,,,C1860315,C536698,,,,
+BMGC_DS11914,BMG_DS040478,,"WAARDENBURG SYNDROME, TYPE IIA",,,,,,,C1860339,,193510,MONDO:0008671,Waardenburg syndrome type 2A,
+BMGC_DS11915,BMG_DS040480,771263004,Tucker syndrome,,,,,,,C1860403,C536923,193240,MONDO:0008665,ptosis-vocal cord paralysis syndrome,Ptosis and vocal cord paralysis syndrome (disorder) | Ptosis and vocal cord paralysis syndrome | Tucker syndrome
+BMGC_DS11916,BMG_DS040481,,Snowflake vitreoretinal degeneration,,,,,DOID:0111570,snowflake vitreoretinal degeneration,C1860405,C536677,193230,MONDO:0008663,snowflake vitreoretinal degeneration,
+BMGC_DS11917,BMG_DS040482,,,,,,,,,C1860446,,,MONDO:0017547,"congenital vertical talus, bilateral",
+BMGC_DS11918,BMG_DS040483,,Vertebral Hypoplasia With Lumbar Kyphosis,,,,,,,C1860463,C566002,192900,MONDO:0008651,vertebral hypoplasia with lumbar kyphosis,
+BMGC_DS11919,BMG_DS040484,,Vertebral fusion posterior lumbosacral blepharoptosis,,,,,,,C1860464,C536344,192800,MONDO:0008650,posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome,
+BMGC_DS11920,BMG_DS040485,,"Venular Insufficiency, Systemic",,,,,,,C1860465,C566004,192700,MONDO:0008649,"venular insufficiency, systemic",
+BMGC_DS11921,BMG_DS040486,,Stoll Alembik Dott syndrome,,,,,,,C1860471,C537497,192445,MONDO:0008645,ventricular extrasystoles with syncopal episodes-perodactyly-robin sequence syndrome,
+BMGC_DS11922,BMG_DS040488,,"Vasculopathy, Retinal, With Cerebral Leukodystrophy",,,,,DOID:0111567,retinal vasculopathy with cerebral leukodystrophy,C1860518,C566007,192315,MONDO:0008641,retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations,
+BMGC_DS11923,BMG_DS040489,,"Vasculitis, Lymphocytic, Nodular",,,,,,,C1860519,C566008,192310,MONDO:0008640,"vasculitis, lymphocytic, nodular",
+BMGC_DS11924,BMG_DS040492,,"Urticaria, Familial Localized Heat",,,,,,,C1860551,C566011,191950,MONDO:0008634,"urticaria, familial localized heat",
+BMGC_DS11925,BMG_DS040493,,"Ureter, Bifid Or Double",,,,,,,C1860586,C566012,191550,MONDO:0008626,"ureter, bifid or double",
+BMGC_DS11926,BMG_DS040495,719041000,Upington disease,,,,,,,C1860596,C536472,191520,MONDO:0008624,Upington disease,Upington disease | Hip dysplasia with enchondromata and ecchondroma syndrome | Hip dysplasia with enchondromata and ecchondroma syndrome (disorder)
+BMGC_DS11927,BMG_DS040496,,Undritz Anomaly,,,,,,,C1860604,C566014,191500,MONDO:0008623,Undritz anomaly,
+BMGC_DS11928,BMG_DS040498,715242008,Ulna metaphyseal dysplasia syndrome,,,,,,,C1860615,C536935,191420,MONDO:0008619,ulna metaphyseal dysplasia syndrome,Ulna metaphyseal dysplasia syndrome (disorder) | Ulna metaphyseal dysplasia syndrome | Rosenberg-Lohr syndrome
+BMGC_DS11929,BMG_DS040500,,Tune Deafness,,,,,,,C1860646,C566019,191200,MONDO:0008615,tune deafness,
+BMGC_DS11930,BMG_DS040502,,Tuberous Sclerosis 2,,,,,DOID:0080325,tuberous sclerosis 2,C1860707,C566021,613254,MONDO:0013199,tuberous sclerosis 2,
+BMGC_DS11931,BMG_DS040503,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7",,,,,DOID:0110313,hypertrophic cardiomyopathy 7,C1860752,,191044;613690,MONDO:0013369,hypertrophic cardiomyopathy 7,
+BMGC_DS11932,BMG_DS040504,,,,,,,,,C1860773,,191000,MONDO:0008611,humerus trochlea aplasia,
+BMGC_DS11933,BMG_DS040505,,,,,,,,,C1860785,,190800,MONDO:0008609,Tristichiasis,
+BMGC_DS11934,BMG_DS040506,,Transient Myeloproliferative Disorder of Down Syndrome,,,,,,,C1860788,C566024,,,,
+BMGC_DS11935,BMG_DS040507,,Triphalangeal thumbs brachyectrodactyly,,,,,,,C1860804,C536564,190680,MONDO:0008607,triphalangeal thumbs-brachyectrodactyly syndrome,
+BMGC_DS11936,BMG_DS040508,733456002,Say Field Coldwell syndrome,,,,,,,C1860805,C536619,190650,MONDO:0008606,Say-field-Coldwell syndrome,Triphalangeal thumb and dislocation of patella syndrome (disorder) | Triphalangeal thumb and dislocation of patella syndrome | Say Field Coldwell syndrome
+BMGC_DS11937,BMG_DS040509,,Triphalangeal Thumb with Double Phalanges,,,,,,,C1860807,C566028,190500,MONDO:0008604,triphalangeal thumb with double phalanges,
+BMGC_DS11938,BMG_DS040510,,Triosephosphate Isomerase Deficiency,,,,,DOID:0050884,triosephosphate isomerase deficiency,C1860808,C566029,615512,MONDO:0014221,triosephosphate isomerase deficiency,
+BMGC_DS11939,BMG_DS040511,,"Triglyceride Storage Disease, Type II",,,,,,,C1860820,C566030,190430,MONDO:0008602,"triglyceride storage disease, type 2",
+BMGC_DS11940,BMG_DS040512,,"Triglyceride Storage Disease, Type I",,,,,,,C1860821,C566031,190420,MONDO:0008601,"triglyceride storage disease, type 1",
+BMGC_DS11941,BMG_DS040514,,"Trichorhinophalangeal Syndrome, Type III",,,,,,,C1860823,C566033,190351,MONDO:0008597,"obsolete trichorhinophalangeal syndrome, type III",
+BMGC_DS11942,BMG_DS040517,,Familial multiple trichodiscomas,,,,,,,C1860850,C536847,190340,MONDO:0008594,familial multiple discoid fibromas,
+BMGC_DS11943,BMG_DS040518,782935003,Neuhauser Daly Magnelli syndrome,,,,,,,C1860860,C536406,190310,MONDO:0008591,tremor-nystagmus-duodenal ulcer syndrome,"Tremor, nystagmus, duodenal ulcer syndrome (disorder) | Tremor, nystagmus, duodenal ulcer syndrome | Neuhauser Daly Magnelli syndrome"
+BMGC_DS11944,BMG_DS040519,,"TREMOR, HEREDITARY ESSENTIAL, 1",,,,,DOID:0111428,essential tremor 1,C1860861,,190300,MONDO:0008590,"tremor, hereditary essential, 1",
+BMGC_DS11945,BMG_DS040520,,"Tremor of Intention, Ataxia, and Lipofuscinosis",,,,,,,C1860872,C566038,190200,MONDO:0008589,"tremor of intention, ataxia, and lipofuscinosis",
+BMGC_DS11946,BMG_DS040521,,,,,,,,,C1860896,,614331,MONDO:0013695,"colorectal cancer, hereditary nonpolyposis, type 6",
+BMGC_DS11947,BMG_DS040522,,,,,,,,,C1860972,,190100,MONDO:0008588,hereditary geniospasm,
+BMGC_DS11948,BMG_DS040523,,NOONAN SYNDROME 3,,,,,,,C1860991,,190070;609942,MONDO:0012371,Noonan syndrome 3,
+BMGC_DS11949,BMG_DS040524,,Esophageal atresia with or without tracheoesophageal fistula,,,,,,,C1861028,C531835,,,,
+BMGC_DS11950,BMG_DS040526,,,,,,,,,C1861058,,189230,MONDO:0008580,"toes, space between first and second",
+BMGC_DS11951,BMG_DS040527,,,,,,,,,C1861059,,189200,MONDO:0008579,"toes, relative length of first and second",
+BMGC_DS11952,BMG_DS040528,,,,,,,,,C1861060,,189150,MONDO:0008578,"toe, rotated fifth",
+BMGC_DS11953,BMG_DS040529,,,,,,,,,C1861061,,189100,MONDO:0008577,"toe, misshapen",
+BMGC_DS11954,BMG_DS040530,,,,,,,,,C1861062,,189000,MONDO:0008576,"toe, fifth, number of phalanges 1N",
+BMGC_DS11955,BMG_DS040531,,,,,,,,,C1861063,,188890,MONDO:0100460,"tobacco addiction, susceptibility to",
+BMGC_DS11956,BMG_DS040532,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9",,,,,DOID:0110315,hypertrophic cardiomyopathy 9,C1861065,,188840;613765,MONDO:0013412,hypertrophic cardiomyopathy 9,
+BMGC_DS11957,BMG_DS040533,,"Tibial Torsion, Bilateral Medial",,,,,,,C1861097,C566045,188800,MONDO:0008573,"tibial torsion, bilateral medial",
+BMGC_DS11958,BMG_DS040534,,"Tibia, Hypoplasia of, with Polydactyly",,,,,,,C1861098,C566046,188740,MONDO:0008572,"tibia, hypoplasia or aplasia of, with polydactyly",
+BMGC_DS11959,BMG_DS040535,,Absence of tibia with polydactyly,,,,,DOID:0111564,hypoplastic or aplastic tibia with polydactyly,C1861099,C535564,,,,
+BMGC_DS11960,BMG_DS040536,,THYROID HORMONE PLASMA MEMBRANE TRANSPORT DEFECT,,,,,,,C1861101,,188560,MONDO:0008568,thyroid hormone plasma membrane transport defect,
+BMGC_DS11961,BMG_DS040537,725462002,Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency,,,,,,,C1861106,,618573,MONDO:0032819,"hypothyroidism, congenital, nongoitrous, 7",Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder) | Resistance to thyrotropin-releasing hormone syndrome | TRH (thyrotropin-releasing hormone) resistance syndrome | Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency
+BMGC_DS11962,BMG_DS040541,,"Thumbs, Stiff, With Brachydactyly Type A1 And Developmental Delay",,,,,,,C1861166,C566053,188201,MONDO:0008563,thumb stiffness-brachydactyly-intellectual disability syndrome,
+BMGC_DS11963,BMG_DS040542,,Thumb Deformity And Alopecia,,,,,,,C1861168,C566054,188150,MONDO:0008562,thumb deformity-alopecia-pigmentation anomaly syndrome,
+BMGC_DS11964,BMG_DS040543,,Thrombophilia due to Activated Protein C Resistance,,,,,DOID:0111902,thrombophilia due to activated protein C resistance,C1861171,C566056,188055,MONDO:0008560,thrombophilia due to activated protein C resistance,
+BMGC_DS11965,BMG_DS040544,,Venous Thromboembolism,Venous Thromboembolism,,,,,,C1861172,D054556,,MONDO:0005399,venous thromboembolism,
+BMGC_DS11966,BMG_DS040545,,Thrombocytopenia 2,,,,,,,C1861185,C536519,188000,MONDO:0008555,thrombocytopenia 2,
+BMGC_DS11967,BMG_DS040546,,"Thrombasthenia-Thrombocytopenia, Hereditary",,,,,,,C1861194,C566060,187900,MONDO:0008553,platelet-type bleeding disorder 17,
+BMGC_DS11968,BMG_DS040547,,"Glanzmann Thrombasthenia, Autosomal Dominant",,,,,,,C1861195,C566061,,,,
+BMGC_DS11969,BMG_DS040549,723556008,Thoracolaryngopelvic dysplasia,,,,,,,C1861197,C536517,187760;187770,MONDO:0008551,thoracolaryngopelvic dysplasia,Thoracolaryngopelvic dysplasia | Barnes syndrome | Thoracolaryngopelvic dysplasia syndrome (disorder) | Thoracolaryngopelvic dysplasia syndrome
+BMGC_DS11970,BMG_DS040550,,"Thoracic Dysostosis, Isolated",,,,,,,C1861204,C566063,187750,MONDO:0008549,"thoracic dysostosis, isolated",
+BMGC_DS11971,BMG_DS040552,,"Thalassemia, Beta+, Silent Allele",,,,,,,C1861232,C566065,187550,MONDO:0008545,"thalassemia, beta+, silent allele",
+BMGC_DS11972,BMG_DS040553,,,,,,,,,C1861233,,187510,MONDO:0008544,tetramelic monodactyly,
+BMGC_DS11973,BMG_DS040554,,Tetralogy of fallot and glaucoma,,,,,,,C1861234,C536501,187501,MONDO:0008543,tetralogy of fallot and glaucoma,
+BMGC_DS11974,BMG_DS040555,,Forebrain Defects,,,,,,,C1861235,C566067,,,,
+BMGC_DS11975,BMG_DS040556,,,,,,,,,C1861237,,187390,MONDO:0008540,extensor tendons of finger anomalies,
+BMGC_DS11976,BMG_DS040557,,"ARTHROGRYPOSIS, DISTAL, TYPE 10",,,,,,,C1861238,,187370,MONDO:0016675,distal arthrogryposis type 10,
+BMGC_DS11977,BMG_DS040559,,"Teeth, Odd Shapes Of",,,,,,,C1861274,C566076,187000,MONDO:0008530,"teeth, odd shapes of",
+BMGC_DS11978,BMG_DS040565,,,,,,,,,C1861296,,186750,MONDO:0008526,talonavicular coalition,
+BMGC_DS11979,BMG_DS040566,,Immunodeficiency due to Defect in CD3-Gamma,,,,,,,C1861297,C566083,,,,
+BMGC_DS11980,BMG_DS040568,,,,,,,,,C1861302,,186600,MONDO:0008524,"syringomas, multiple",
+BMGC_DS11981,BMG_DS040569,699861000,"Granulomatous inflammatory arthritis, dermatitis and uveitis, familial",,,,,,,C1861303,,,,,"Arthrocutaneouveal granulamotosis | Familial juvenile systemic granulomatosis | Familial granulomatosis, Blau type | Pediatric granulomatous arthritis | Familial granulomatous inflammatory arthritis, dermatitis and uveitis | Familial granulomatous inflammatory arthritis, dermatitis and uveitis (disorder) | Granulomatous inflammatory arthritis, dermatitis and uveitis, familial | Paediatric granulomatous arthritis"
+BMGC_DS11982,BMG_DS040570,,"Synovial Chondromatosis, Familial, with Dwarfism",,,,,,,C1861304,C566087,186575,MONDO:0008522,"synovial chondromatosis, familial, with dwarfism",
+BMGC_DS11983,BMG_DS040571,,TARSAL-CARPAL COALITION SYNDROME,,,,,DOID:0050789,tarsal-carpal coalition syndrome,C1861305,,186570;602991,MONDO:0008521,tarsal-carpal coalition syndrome,
+BMGC_DS11984,BMG_DS040573,,"Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly",,,,,,,C1861313,C566090,186550,MONDO:0008520,brachydactyly-elbow wrist dysplasia syndrome,
+BMGC_DS11985,BMG_DS040575,,Syndactyly-Polydactyly-Earlobe Syndrome,,,,,,,C1861347,C566091,186350,MONDO:0008517,syndactyly-polydactyly-ear lobe syndrome,
+BMGC_DS11986,BMG_DS040576,,,,,,,DOID:0111819,syndactyly type 5,C1861348,,186300,MONDO:0008516,syndactyly type 5,
+BMGC_DS11987,BMG_DS040577,,"Syndactyly, Type IV",,,,,DOID:0111818,syndactyly type 4,C1861355,C566092,186200,MONDO:0008515,syndactyly type 4,
+BMGC_DS11988,BMG_DS040578,,"SYNDACTYLY, TYPE III",,,,,DOID:0111817,syndactyly type 3,C1861366,,186100;121014,MONDO:0008514,syndactyly type 3,
+BMGC_DS11989,BMG_DS040580,,"Syndactyly, Type I",,,,,,,C1861380,C566096,185900,MONDO:0008512,syndactyly type 1,
+BMGC_DS11990,BMG_DS040581,,,,,,,,,C1861385,,,MONDO:0008511,proximal symphalangism,
+BMGC_DS11991,BMG_DS040583,,,,,,,,,C1861401,,185700,MONDO:0008509,distal symphalangism,
+BMGC_DS11992,BMG_DS040584,,"Symphalangism, C. S. Lewis Type",,,,,,,C1861404,C566100,185650,MONDO:0008508,"symphalangism, C. S. Lewis type",
+BMGC_DS11993,BMG_DS040586,,Symphalangism of Toes,,,,,,,C1861418,C566101,185600,MONDO:0008506,symphalangism of toes,
+BMGC_DS11994,BMG_DS040588,,"Sulfhemoglobinemia, Congenital",,,,,,,C1861437,C566102,185460,MONDO:0008502,"sulfhemoglobinemia, congenital",
+BMGC_DS11995,BMG_DS040590,,"Striae Distensae, Familial",,,,,,,C1861447,C566104,185200,MONDO:0008500,"striae distensae, familial",
+BMGC_DS11996,BMG_DS040592,,,,,,,,,C1861449,,185100,MONDO:0008498,"strabismus, susceptibility to",
+BMGC_DS11997,BMG_DS040594,,Stormorken Syndrome,,,,,DOID:0060354,Stormorken syndrome,C1861451,C566108,185070,MONDO:0008497,Stormorken syndrome,
+BMGC_DS11998,BMG_DS040596,,Pseudohyperkalemia Cardiff,,,,,,,C1861453,C535827,185020,MONDO:0008494,cryohydrocytosis,
+BMGC_DS11999,BMG_DS040598,,,,,,,,,C1861455,,185000,MONDO:0008493,overhydrated hereditary stomatocytosis,
+BMGC_DS12000,BMG_DS040599,,Stiff Skin Syndrome,,,,,DOID:0111561,stiff skin syndrome,C1861456,C566112,184900,MONDO:0008492,stiff skin syndrome,
+BMGC_DS12001,BMG_DS040600,,PROGRESSIVE ENCEPHALOMYELITIS WITH RIGIDITY,,,,,,,C1861457,,184850,MONDO:0018581,progressive encephalomyelitis with rigidity and myoclonus,
+BMGC_DS12002,BMG_DS040601,,"Stickler syndrome, type 3",,,,,,,C1861481,C537494,,,,
+BMGC_DS12003,BMG_DS040603,,COLCHICINE RESISTANCE,,,,,,,C1861502,,120080;171050,,,
+BMGC_DS12004,BMG_DS040604,,Cochleosaccular degeneration of the inner ear and progressive cataracts,,,,,,,C1861512,C536432,120040,MONDO:0007346,cochleosaccular degeneration-cataract syndrome,
+BMGC_DS12005,BMG_DS040605,,"Cluster Headache, Familial",,,,,,,C1861513,C566117,119915,MONDO:0007344,"cluster headache, familial",
+BMGC_DS12006,BMG_DS040606,719471002,Cleidorhizomelic syndrome,,,,,,,C1861515,C536428,119650,MONDO:0007341,cleidorhizomelic syndrome,Cleidorhizomelic syndrome (disorder) | Cleidorhizomelic syndrome | Rhizomelic shortness with clavicular defect | Wallis Zieff Goldblatt syndrome
+BMGC_DS12007,BMG_DS040608,,Blepharo-cheilo-dontic syndrome,,,,,DOID:0080344,blepharocheilodontic syndrome,C1861536,C536188,,MONDO:0007339,blepharocheilodontic syndrome,
+BMGC_DS12008,BMG_DS040609,,OROFACIAL CLEFT 1,,,,,,,C1861537,,119530,MONDO:0007335,orofacial cleft 1,
+BMGC_DS12009,BMG_DS040610,,Split-Hand-Foot Malformation With Long Bone Deficiency 1,,,,,,,C1861553,C536425,119100,MONDO:0007332,split-hand/foot malformation with long bone deficiency 1,
+BMGC_DS12010,BMG_DS040611,,"Cirrhosis, Familial",,,,,,,C1861556,C566123,215600,MONDO:0007329,"cirrhosis, familial",
+BMGC_DS12011,BMG_DS040614,,"Chylomicronemia, Familial, due to Circulating Inhibitor of Lipoprotein Lipase",,,,,,,C1861560,C566126,118830,MONDO:0007327,"chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase",
+BMGC_DS12012,BMG_DS040615,,"Choreoathetosis, Familial Inverted",,,,,,,C1861569,C566127,118750,MONDO:0007325,"choreoathetosis, familial inverted",
+BMGC_DS12013,BMG_DS040622,,Charcot-Marie-Tooth disease and deafness,,,,,,,C1861669,C538078,214370,MONDO:0008960,Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome,
+BMGC_DS12014,BMG_DS040624,,"Charcot-Marie-Tooth Disease, Axonal, Type 2a1",,,,,,,C1861678,C566138,118210,MONDO:0007308,Charcot-Marie-Tooth disease type 2A1,
+BMGC_DS12015,BMG_DS040625,,,,,,,,,C1861689,,118100,MONDO:0007306,"Klippel-Feil syndrome 1, autosomal dominant",
+BMGC_DS12016,BMG_DS040626,,Cervical Vertebral Dysplasia,,,,,,,C1861693,C566140,118005,MONDO:0007305,cervical vertebral dysplasia,
+BMGC_DS12017,BMG_DS040627,,,,,,,,,C1861694,,118000,MONDO:0007304,cervical vertebral Bridge,
+BMGC_DS12018,BMG_DS040628,,Cervical Hypertrichosis with Underlying Kyphoscoliosis,,,,,,,C1861695,C566142,117850,MONDO:0007302,cervical hypertrichosis with underlying kyphoscoliosis,
+BMGC_DS12019,BMG_DS040629,,"EAR WAX, WET/DRY",,,,,,,C1861696,,117800;607040,,,
+BMGC_DS12020,BMG_DS040631,,Spinocerebellar Ataxia 29,,,,,,,C1861732,C537206,117360,MONDO:0007298,spinocerebellar ataxia type 29,
+BMGC_DS12021,BMG_DS040632,,"Dementia, familial Danish",,,,,,,C1861735,C538209,117300,MONDO:0007297,ADan amyloidosis,
+BMGC_DS12022,BMG_DS040633,,Spinocerebellar Ataxia 31,,,,,,,C1861736,C566146,117210,MONDO:0007296,spinocerebellar ataxia type 31,
+BMGC_DS12023,BMG_DS040637,,"Multiminicore Disease, Moderate, with Hand Involvement",,,,,,,C1861753,C566147,,MONDO:0015793,moderate multiminicore disease with hand involvement,
+BMGC_DS12024,BMG_DS040638,,Median Arcuate Ligament Syndrome,Median Arcuate Ligament Syndrome,,,,DOID:9892,median arcuate ligament syndrome,C1861783,D000074742,116870,MONDO:0004914,celiac artery stenosis from compression by median arcuate ligament of diaphragm,
+BMGC_DS12025,BMG_DS040639,,Cavernous Malformations of CNS and Retina,,,,,,,C1861785,C566152,,,,
+BMGC_DS12026,BMG_DS040640,,Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated With Cerebral Capillary Malformations,,,,,,,C1861786,C566153,,,,
+BMGC_DS12027,BMG_DS040642,,"CATARACT, MARNER TYPE",,,,,,,C1861821,,116800,,,
+BMGC_DS12028,BMG_DS040643,,"CATARACT, POSTERIOR POLAR, 1",,,,,,,C1861825,,116600,MONDO:0007288,cataract 6 multiple types,
+BMGC_DS12029,BMG_DS040645,,"Cataract, Nuclear Diffuse Nonprogressive",,,,,,,C1861827,C566157,,,,
+BMGC_DS12030,BMG_DS040646,,"Cataract, Zonular Pulverulent 1",,,,,,,C1861828,C566158,116200,MONDO:0007285,cataract 1 multiple types,
+BMGC_DS12031,BMG_DS040647,,Cataract microcornea syndrome,,,,,,,C1861829,C538287,,MONDO:0015300,cataract - microcornea syndrome,
+BMGC_DS12032,BMG_DS040650,,"CATARACT, CONGENITAL, VOLKMANN TYPE",,,,,,,C1861833,,115665,MONDO:0007280,cataract 8 multiple types,
+BMGC_DS12033,BMG_DS040652,,,,,,,,,C1861847,,115400,MONDO:0007274,carpal displacement,
+BMGC_DS12034,BMG_DS040653,,PARAGANGLIOMAS 4,,,,,,,C1861848,,115310,MONDO:0007273,paragangliomas 4,
+BMGC_DS12035,BMG_DS040655,,"Cardiomyopathy, Familial Restrictive, 1",,,,,,,C1861861,C566168,115210,MONDO:0007270,"cardiomyopathy, familial restrictive, 1",
+BMGC_DS12036,BMG_DS040656,,,,,,,,,C1861862,,115197,MONDO:0007268,hypertrophic cardiomyopathy 4,
+BMGC_DS12037,BMG_DS040657,,"Cardiomyopathy, Familial Hypertrophic, 3",,,,,,,C1861863,C566170,115196,MONDO:0007267,hypertrophic cardiomyopathy 3,
+BMGC_DS12038,BMG_DS040658,,"Cardiomyopathy, Familial Hypertrophic, 2",,,,,,,C1861864,C566171,115195,MONDO:0007266,hypertrophic cardiomyopathy 2,
+BMGC_DS12039,BMG_DS040659,,Familial Sudden Death,,,,,,,C1861884,C566172,,,,
+BMGC_DS12040,BMG_DS040660,,Monocyte Esterase Deficiency,,,,,,,C1861889,C566173,,,,
+BMGC_DS12041,BMG_DS040662,,Carabelli Anomaly of Maxillary Molar Teeth,,,,,,,C1861897,C566175,114700,MONDO:0007261,Carabelli anomaly of maxillary molar teeth,
+BMGC_DS12042,BMG_DS040663,,Car Factor Deficiency,,,,,,,C1861898,C566176,114650,MONDO:0007260,Car factor deficiency,
+BMGC_DS12043,BMG_DS040664,,"CANINE TEETH, ABSENCE OF UPPER PERMANENT",,,,,,,C1861899,,114600,MONDO:0007258,"canine teeth, absence of upper permanent",
+BMGC_DS12044,BMG_DS040665,,,,,,,,,C1861915,,114450,MONDO:0007253,"cancer, familial, with in vitro Radioresistance",
+BMGC_DS12045,BMG_DS040666,,CAMPOMELIC DYSPLASIA,,,,,DOID:0050463,campomelic dysplasia,C1861922,,114290;608160,MONDO:0007251,campomelic dysplasia,
+BMGC_DS12046,BMG_DS040667,,Acampomelic Campomelic Dysplasia,Campomelic Dysplasia,,,,DOID:0050463,campomelic dysplasia,C1861923,D055036,,,,
+BMGC_DS12047,BMG_DS040668,,,,,,,,,C1861963,,114150,MONDO:0007249,camptobrachydactyly,
+BMGC_DS12048,BMG_DS040669,,"Callosities, Hereditary Painful",,,,,,,C1861964,C566180,114140,MONDO:0007248,hereditary painful callosities,
+BMGC_DS12049,BMG_DS040670,,"Idiopathic basal ganglia calcification, childhood onset",,,,,,,C1861967,C536276,114100,MONDO:0007247,"basal ganglia calcification, idiopathic, childhood-onset",
+BMGC_DS12050,BMG_DS040671,,"Calcific Aortic Disease with Immunologic Abnormalities, Familial",,,,,,,C1861974,C566182,114065,MONDO:0007246,"calcific aortic disease with immunologic abnormalities, familial",
+BMGC_DS12051,BMG_DS040672,,"Cafe au lait spots, multiple",,,,,,,C1861975,C537421,114030,MONDO:0007245,"cafe au lait spots, multiple",
+BMGC_DS12052,BMG_DS040675,,"Heart Block, Nonprogressive",,,,,,,C1861983,C566185,,,,
+BMGC_DS12053,BMG_DS040676,,"Cardiac Conduction Defect, Nonprogressive",,,,,,,C1861984,C566186,,,,
+BMGC_DS12054,BMG_DS040681,,Brachymorphism-onychodysplasia-dysphalangism syndrome,,,,,,,C1862082,C536242,113477,MONDO:0007230,Brachymorphism-onychodysplasia-dysphalangism syndrome,
+BMGC_DS12055,BMG_DS040685,,Brachydactyly-Nystagmus-Cerebellar Ataxia,,,,,,,C1862099,C566192,113400,MONDO:0007226,brachydactyly-nystagmus-cerebellar ataxia syndrome,
+BMGC_DS12056,BMG_DS040686,,Fibular aplasia ectrodactyly,,,,,,,C1862100,C537930,113310,MONDO:0007225,fibular aplasia-ectrodactyly syndrome,
+BMGC_DS12057,BMG_DS040687,,"Brachydactyly, Type E, with Atrial Septal Defect, Type II",,,,,,,C1862101,C566193,113301,MONDO:0007224,"brachydactyly, type E, with atrial septal defect, type 2",
+BMGC_DS12058,BMG_DS040688,,,,,,,,,C1862102,,113300,MONDO:0007223,brachydactyly type E1,
+BMGC_DS12059,BMG_DS040689,,,,,,,DOID:0110970,brachydactyly type C,C1862103,,113100,MONDO:0007221,brachydactyly type C,
+BMGC_DS12060,BMG_DS040690,,,,,,,,,C1862112,,113000,MONDO:0007220,brachydactyly type B1,
+BMGC_DS12061,BMG_DS040691,715722003,Brachydactyly type A6,,,,,DOID:0110968,brachydactyly type A6,C1862130,C537092,112910,MONDO:0007219,Osebold-Remondini syndrome,Brachydactyly type A6 (disorder) | Brachydactyly type A6 | Osebold Remondini syndrome
+BMGC_DS12062,BMG_DS040693,,,,,,,,,C1862139,,112800,MONDO:0007218,brachydactyly type A4,
+BMGC_DS12063,BMG_DS040694,,,,,,,,,C1862140,,112700,MONDO:0007217,brachydactyly type A3,
+BMGC_DS12064,BMG_DS040695,715720006,Brachydactyly type A1,,,,,DOID:0110964,brachydactyly type A1,C1862151,C537088,MTHU019237;112500,MONDO:0007215,brachydactyly type A1,Brachydactyly type A1 (disorder) | Brachydactyly type A1 | Brachydactyly Farabee type
+BMGC_DS12065,BMG_DS040696,,Brachydactyly preaxial with hallux varus and thumb abduction,,,,,,,C1862162,C537087,112450,MONDO:0007214,brachydactyly-preaxial hallux varus syndrome,
+BMGC_DS12066,BMG_DS040699,,Brachydactyly with hypertension,,,,,DOID:0111247,hypertension and brachydactyly syndrome,C1862170,C537095,112410,MONDO:0007211,brachydactyly-arterial hypertension syndrome,
+BMGC_DS12067,BMG_DS040700,,"Brachmann-De Lange-Like Facial Changes With Microcephaly, Metatarsus Adductus, And Developmental Delay",,,,,,,C1862171,C566206,112370,MONDO:0007210,"Brachmann-de Lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay",
+BMGC_DS12068,BMG_DS040701,715532007,Weismann Netter syndrome,,,,,,,C1862172,C537082,112350,MONDO:0007209,Weismann-Netter syndrome,Weismann Netter syndrome (disorder) | Weismann Netter syndrome | Anterior bowing of legs with dwarfism
+BMGC_DS12069,BMG_DS040702,,,,,,,,,C1862176,,112270,MONDO:0007206,"bone pain, periodic",
+BMGC_DS12070,BMG_DS040703,,Diaphyseal medullary stenosis with malignant fibrous histiocytoma,,,,,DOID:0080664,diaphyseal medullary stenosis with malignant fibrous histiocytoma,C1862177,C536169,112250,MONDO:0007205,diaphyseal medullary stenosis-bone malignancy syndrome,
+BMGC_DS12071,BMG_DS040704,389199001,Cole Carpenter syndrome,,,,,DOID:0060438,Cole-Carpenter syndrome,C1862178,C535963,,MONDO:0016085,Cole-Carpenter syndrome,"Cole-Carpenter dysplasia (disorder) | Cole-Carpenter dysplasia | Bone fragility, craniosynostosis, proptosis, hydrocephalus syndrome | Cole Carpenter syndrome"
+BMGC_DS12072,BMG_DS040708,,Blepharoptosis myopia ectopia lentis,,,,,,,C1862259,C536236,110150,MONDO:0007202,blepharoptosis-myopia-ectopia lentis syndrome,
+BMGC_DS12073,BMG_DS040709,,Bpes With Ovarian Failure,,,,,,,C1862262,C566222,,,,
+BMGC_DS12074,BMG_DS040710,,Bpes Without Ovarian Failure,,,,,,,C1862263,C566222,,,,
+BMGC_DS12075,BMG_DS040711,,Bpes With Duane Retraction Syndrome,,,,,,,C1862264,C566222,,,,
+BMGC_DS12076,BMG_DS040712,,"Blepharochalasis, Superior",,,,,,,C1862275,C566223,110000,MONDO:0007199,"blepharochalasis, superior",
+BMGC_DS12077,BMG_DS040714,,"Basilar Impression, Primary",,,,,,,C1862299,C566226,109500,MONDO:0007188,primary basilar invagination,
+BMGC_DS12078,BMG_DS040718,,"Ovalocytosis, Malaysian-Melanesian-Filipino Type",,,,,,,C1862322,C566231,166900,MONDO:0008165,southeast Asian ovalocytosis,
+BMGC_DS12079,BMG_DS040721,,Axial osteomalacia,,,,,DOID:0080039,axial osteomalacia,C1862372,C537791,109130,MONDO:0007181,axial osteomalacia,
+BMGC_DS12080,BMG_DS040722,,"Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities",,,,,,,C1862373,C566234,109120,MONDO:0007180,"Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities",
+BMGC_DS12081,BMG_DS040723,,Aurocephalosyndactyly,,,,,,,C1862380,C566235,109050,MONDO:0007178,aurocephalosyndactyly,
+BMGC_DS12082,BMG_DS040724,,Auriculoosteodysplasia,,,,,,,C1862381,C538271,109000,MONDO:0007177,auriculoosteodysplasia,
+BMGC_DS12083,BMG_DS040725,,SVEINSSON CHORIORETINAL ATROPHY,,,,,DOID:0111228,Sveinsson chorioretinal atrophy,C1862382,,108985;189967,MONDO:0007176,helicoid peripapillary chorioretinal degeneration,
+BMGC_DS12084,BMG_DS040726,,Atrial Tachyarrhythmia with Short PR Interval,,,,,,,C1862387,C566237,108950,MONDO:0007174,Lown-Ganong-Levine syndrome,
+BMGC_DS12085,BMG_DS040727,,,,,,,,,C1862389,,108800,MONDO:0007172,atrial septal defect 1,
+BMGC_DS12086,BMG_DS040728,,"Atrial Fibrillation, Familial, 4",,,,,,,C1862394,C566244,611493,MONDO:0012677,"atrial fibrillation, familial, 4",
+BMGC_DS12087,BMG_DS040729,,Ataxia with Fasciculations,,,,,,,C1862440,C566246,108700,MONDO:0007166,ataxia with fasciculations,
+BMGC_DS12088,BMG_DS040730,,"Ataxia, Spastic, with Congenital Miosis",,,,,,,C1862441,C566247,108650,MONDO:0007165,spastic ataxia 7,
+BMGC_DS12089,BMG_DS040732,,,,,,,,,C1862459,,108420,MONDO:0007161,spermatogenic failure 2,
+BMGC_DS12090,BMG_DS040735,,Arthrogryposis-like hand anomaly and sensorineural deafness,,,,,DOID:0111609,distal arthrogryposis type 6,C1862471,C535386,108200,MONDO:0007159,arthrogryposis-like hand anomaly-sensorineural deafness syndrome,
+BMGC_DS12091,BMG_DS040736,715217004,Oculomelic amyoplasia,,,,,DOID:0111608,distal arthrogryposis type 5,C1862472,C537737,108145,MONDO:0007158,arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome,Distal arthrogryposis type 5 (disorder) | Distal arthrogryposis type 5 | Arthrogryposis with oculomotor limitation and electroretinal anomaly | Distal arthrogryposis with ophthalmoplegia | Oculomelic amyoplasia
+BMGC_DS12092,BMG_DS040738,,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 1",,,,,,,C1862511,C566254,107970,MONDO:0007152,arrhythmogenic right ventricular dysplasia 1,
+BMGC_DS12093,BMG_DS040740,,,,,,,,,C1862534,,107900,MONDO:0007151,"arms, malformation of",
+BMGC_DS12094,BMG_DS040748,,,,,,,,,C1862591,,,MONDO:0800425,"coronary artery disease, severe, susceptibility to",
+BMGC_DS12095,BMG_DS040749,60193003,Familial hypobetalipoproteinemia,,,,,,,C1862596,,,,,Familial hypobetalipoproteinemia | Familial hypobetalipoproteinaemia | Familial hypobetalipoproteinemia (disorder)
+BMGC_DS12096,BMG_DS040750,,,,,,,,,C1862632,,107700,MONDO:0007148,"appendicitis, proneness to",
+BMGC_DS12097,BMG_DS040751,,"Aortic Arch Interruption, Facial Palsy, and Retinal Coloboma",,,,,,,C1862681,C566271,107550,MONDO:0007144,"aortic arch interruption, facial palsy, and retinal coloboma",
+BMGC_DS12098,BMG_DS040752,,Aortic arch anomaly with peculiar facies and mental retardation,,,,,,,C1862682,C537785,107500,MONDO:0007143,aortic arch anomaly-facial dysmorphism-intellectual disability syndrome,
+BMGC_DS12099,BMG_DS040753,,Townes-Brocks-Branchiootorenal-Like Syndrome,,,,,,,C1862683,C566272,,,,
+BMGC_DS12100,BMG_DS040754,,,,,,,,,C1862839,,,MONDO:0019503,anterior segment dysgenesis,
+BMGC_DS12101,BMG_DS040756,,Anonychia-onychodystrophy with hypoplasia or absence of distal phalanges,,,,,,,C1862841,C537766,106995,MONDO:0007134,Cooks syndrome,
+BMGC_DS12102,BMG_DS040758,,Anonychia-Ectrodactyly,,,,,,,C1862843,C566277,106900,MONDO:0007132,anonychia-ectrodactyly,
+BMGC_DS12103,BMG_DS040759,,Anonychia with Flexural Pigmentation,,,,,,,C1862844,C566278,106750,MONDO:0007131,anonychia with flexural pigmentation,
+BMGC_DS12104,BMG_DS040760,,,,,,,,,C1862852,,106300,MONDO:0007126,"spondyloarthropathy, susceptibility to, 1",
+BMGC_DS12105,BMG_DS040761,,,,,,,,,C1862866,,106250,MONDO:0007123,ankyloblepharon filiforme adnatum-cleft palate syndrome,
+BMGC_DS12106,BMG_DS040762,,"Aniridia, Microcornea, And Spontaneously Reabsorbed Cataract",,,,,,,C1862867,C566280,106230,MONDO:0007121,"aniridia, microcornea, and spontaneously Reabsorbed cataract",
+BMGC_DS12107,BMG_DS040763,,Aniridia and Absent Patella,,,,,,,C1862868,C566281,106220,MONDO:0007120,aniridia-absent patella syndrome,
+BMGC_DS12108,BMG_DS040764,,Hereditary Angioedema Type II,Hereditary Angioedema Types I and II,,,,,,C1862892,D056829,,,,
+BMGC_DS12109,BMG_DS040767,,"Aneurysm, Intracranial Berry, 1",,,,,,,C1862932,C566284,105800,MONDO:0007111,"aneurysm, intracranial berry type 1",
+BMGC_DS12110,BMG_DS040771,,AMYOTROPHIC LATERAL SCLEROSIS 1,,,,,,,C1862939,,105400;147450,MONDO:0007103,amyotrophic lateral sclerosis type 1,
+BMGC_DS12111,BMG_DS040773,,"Amyotrophic Lateral Sclerosis, Sporadic",,,,,,,C1862941,C531617,,MONDO:0005145,sporadic amyotrophic lateral sclerosis,
+BMGC_DS12112,BMG_DS040774,,Amyotrophic Dystonic Paraplegia,,,,,,,C1862956,C566292,105300,MONDO:0007102,amyotrophic dystonic paraplegia,
+BMGC_DS12113,BMG_DS040776,,"Amelogenesis Imperfecta, Type IV",,,,,,,C1863012,C566293,104510,MONDO:0007093,hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism,
+BMGC_DS12114,BMG_DS040777,,Amelia and Terminal Transverse Hemimelia,,,,,,,C1863014,C566294,104400,MONDO:0007091,amelia and terminal transverse hemimelia,
+BMGC_DS12115,BMG_DS040778,,"Amastia, Bilateral, With Ureteral Triplication And Dysmorphism",,,,,,,C1863015,C566295,104350,MONDO:0007090,"amastia, bilateral, with ureteral triplication and dysmorphism",
+BMGC_DS12116,BMG_DS040779,,ALZHEIMER DISEASE 2,,,,,,,C1863051,,104310,MONDO:0007089,Alzheimer disease 2,
+BMGC_DS12117,BMG_DS040780,,"ALZHEIMER DISEASE, FAMILIAL, 1",,,,,DOID:0080348,Alzheimer's disease 1,C1863052,,104300;104760,MONDO:0007088,Alzheimer disease type 1,
+BMGC_DS12118,BMG_DS040782,,alpha-Fetoprotein Deficiency,,,,,,,C1863081,C566300,615969,MONDO:0014424,obsolete congenital deficiency in alpha-fetoprotein,
+BMGC_DS12119,BMG_DS040784,,"Alopecia, Familial Focal",,,,,,,C1863092,C566301,104110,MONDO:0007084,familial focal alopecia,
+BMGC_DS12120,BMG_DS040785,,Alopecia congenita keratosis palmoplantaris,,,,,DOID:0111244,palmoplantar keratoderma and congenital alopecia 1,C1863093,C537050,,MONDO:0022417,alopecia congenita keratosis palmoplantaris,
+BMGC_DS12121,BMG_DS040786,,ALOPECIA AREATA 1,,,,,,,C1863094,,104000,MONDO:0007082,alopecia areata 1,
+BMGC_DS12122,BMG_DS040787,,Dysalbuminemic Hyperthyroxinemia,,,,,,,C1863119,C566305,,,,
+BMGC_DS12123,BMG_DS040789,,Hypoglossia-Hypodactylia,,,,,,,C1863203,C566308,103300,MONDO:0007073,Hypoglossia-hypodactyly syndrome,
+BMGC_DS12124,BMG_DS040790,,ADULT SYNDROME,,,,,DOID:0050601,ADULT syndrome,C1863204,,103285;603273,MONDO:0007072,ADULT syndrome,
+BMGC_DS12125,BMG_DS040791,,"Adenosine Triphosphate, Elevated, Of Erythrocytes",,,,,,,C1863224,C566310,102900,MONDO:0007067,pyruvate kinase hyperactivity,
+BMGC_DS12126,BMG_DS040793,,"Adenosine Deaminase, Elevated, Hemolytic Anemia Due To",,,,,,,C1863235,C566314,301083;102730,MONDO:0020458,hemolytic anemia due to erythrocyte adenosine deaminase overproduction,
+BMGC_DS12127,BMG_DS040794,,,,,,,,,C1863236,,102700,MONDO:0007064,"severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency",
+BMGC_DS12128,BMG_DS040795,,Partial adenosine deaminase deficiency,,,,,,,C1863239,C531816,,,,
+BMGC_DS12129,BMG_DS040796,,"Acropectorovertebral Dysplasia, F-Form",,,,,,,C1863307,C566319,102510,MONDO:0007058,Acropectorovertebral dysplasia,
+BMGC_DS12130,BMG_DS040797,,"Acroleukopathy, Symmetric",,,,,,,C1863342,C566322,102000,MONDO:0007049,"acroleukopathy, symmetric",
+BMGC_DS12131,BMG_DS040798,,"Acrokeratoderma, Hereditary Papulotranslucent",,,,,DOID:0060360,hereditary papulotranslucent acrokeratoderma,C1863343,C566323,101840,MONDO:0007046,hereditary papulotranslucent acrokeratoderma,
+BMGC_DS12132,BMG_DS040799,,Saethre-Chotzen Syndrome with Eyelid Anomalies,,,,,,,C1863370,C566325,,,,
+BMGC_DS12133,BMG_DS040800,,Apert-Crouzon Disease,Acrocephalosyndactylia,,,,,,C1863389,D000168,,,,
+BMGC_DS12134,BMG_DS040802,,Autosomal dominant compelling helio ophthalmic outburst syndrome,,,,,,,C1863416,C535300,100820,MONDO:0007038,Achoo syndrome,
+BMGC_DS12135,BMG_DS040803,,"HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE",,,,,,,C1863512,,603813,MONDO:0011374,"hypercholesterolemia, familial, 4",
+BMGC_DS12136,BMG_DS040807,,Stargardt disease 4,,,,,,,C1863534,C535521,603786,MONDO:0011370,Stargardt disease 4,
+BMGC_DS12137,BMG_DS040808,,"HYPERCHOLESTEROLEMIA, FAMILIAL, 3",,,,,,,C1863551,,603776;607786,MONDO:0011369,"hypercholesterolemia, autosomal dominant, 3",
+BMGC_DS12138,BMG_DS040810,,Young Simpson syndrome,,,,,DOID:0060290,"Ohdo syndrome,  SBBYS variant",C1863557,C536717,603736,MONDO:0011365,"blepharophimosis - intellectual disability syndrome, SBBYS type",
+BMGC_DS12139,BMG_DS040811,,"Deafness, Autosomal Recessive 16",,,,,,,C1863561,C566339,603720,MONDO:0011364,autosomal recessive nonsyndromic hearing loss 16,
+BMGC_DS12140,BMG_DS040813,,Hereditary Myopathy with Early Respiratory Failure,,,,,,,C1863599,C566343,607569;603689,MONDO:0011362,"myopathy, myofibrillar, 9, with early respiratory failure",
+BMGC_DS12141,BMG_DS040814,,,,,,,,,C1863600,,603688,MONDO:0011361,prostate cancer/brain cancer susceptibility,
+BMGC_DS12142,BMG_DS040815,,"DEAFNESS, AUTOSOMAL RECESSIVE 14",,,,,,,C1863613,,603678,MONDO:0011360,autosomal recessive nonsyndromic hearing loss 14,
+BMGC_DS12143,BMG_DS040816,,ACROMELIC FRONTONASAL DYSOSTOSIS,,,,,,,C1863616,,603671;615951,MONDO:0011359,acromelic frontonasal dysostosis,
+BMGC_DS12144,BMG_DS040822,,Cone-Rod Dystrophy 7,,,,,DOID:0111012,cone-rod dystrophy 7,C1863634,C566350,603649,MONDO:0011355,cone-rod dystrophy 7,
+BMGC_DS12145,BMG_DS040826,,"Deafness, Autosomal Recessive 21",,,,,,,C1863655,C566353,603629,MONDO:0011351,autosomal recessive nonsyndromic hearing loss 21,
+BMGC_DS12146,BMG_DS040827,,"DEAFNESS, AUTOSOMAL DOMINANT 17",,,,,,,C1863659,,160775;603622,MONDO:0011350,autosomal dominant nonsyndromic hearing loss 17,
+BMGC_DS12147,BMG_DS040829,,Craniosynostosis with Ectopia Lentis,,,,,,,C1863678,C566357,603595,MONDO:0011347,craniosynostosis with ectopia lentis,
+BMGC_DS12148,BMG_DS040830,,"Xanthinuria, Type II",,,,,DOID:0070453,xanthinuria type II,C1863688,C566358,603592,MONDO:0011346,xanthinuria type II,
+BMGC_DS12149,BMG_DS040834,,"Spastic paraplegia 8, autosomal dominant",,,,,,,C1863704,C580458,603563,MONDO:0011339,hereditary spastic paraplegia 8,
+BMGC_DS12150,BMG_DS040835,,"HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2",,,,,DOID:0110922,familial hemophagocytic lymphohistiocytosis 2,C1863727,,170280;603553,MONDO:0011337,familial hemophagocytic lymphohistiocytosis 2,
+BMGC_DS12151,BMG_DS040836,,"Hemophagocytic lymphohistiocytosis, familial, 4",,,,,,,C1863728,C537252,603552,MONDO:0011336,familial hemophagocytic lymphohistiocytosis 4,
+BMGC_DS12152,BMG_DS040837,766820007,Spondyloepimetaphyseal dysplasia with multiple dislocations,,,,,,,C1863732,C535784,603546,MONDO:0011335,spondyloepimetaphyseal dysplasia with multiple dislocations,Spondyloepimetaphyseal dysplasia with multiple dislocations | Spondyloepimetaphyseal dysplasia with multiple dislocations (disorder) | Spondyloepimetaphyseal dysplasia with joint laxity type 2 | Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic type | Spondyloepimetaphyseal dysplasia with joint laxity Hall type | Spondyloepimetaphyseal dysplasia with multiple dislocations Hall type
+BMGC_DS12153,BMG_DS040838,,,,,,,,,C1863752,,,MONDO:0023069,enlarged vestibular aqueduct syndrome,
+BMGC_DS12154,BMG_DS040839,,LIMB-MAMMARY SYNDROME,,,,,,,C1863753,,603273;603543,MONDO:0011334,limb-mammary syndrome,
+BMGC_DS12155,BMG_DS040842,,"Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema",,,,,,,C1863769,C566369,,,,
+BMGC_DS12156,BMG_DS040843,715437003,Neuronal intranuclear inclusion disease,,,,,,,C1863843,C537395,603472,MONDO:0011327,neuronal intranuclear inclusion disease,Neuronal intranuclear inclusion disease (disorder) | Neuronal intranuclear inclusion disease
+BMGC_DS12157,BMG_DS040844,,Adult-onset citrullinemia type 2,,,,,,,C1863844,C538053,,MONDO:0016603,citrullinemia type II,
+BMGC_DS12158,BMG_DS040846,763132003,Coloboma of superior eyelid,,,,,,,C1863872,,,MONDO:0015480,coloboma of superior eyelid,Coloboma of superior eyelid | Coloboma of upper eyelid | Coloboma of superior eyelid (disorder) | Superior palpebral coloboma
+BMGC_DS12159,BMG_DS040847,,"Arhinia, choanal atresia, and microphthalmia",,,,,,,C1863878,C537429,603457,MONDO:0011323,"arhinia, choanal atresia, and microphthalmia",
+BMGC_DS12160,BMG_DS040850,,,,,,,,,C1863881,,603438,MONDO:0011320,radioulnar synostosis-microcephaly-scoliosis syndrome,
+BMGC_DS12161,BMG_DS040857,,Megalancephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome,,,,,,,C1863924,C566381,,,,
+BMGC_DS12162,BMG_DS040859,,"Glaucoma 1, Open Angle, F",,,,,,,C1863926,C566383,603383,MONDO:0011311,"obsolete glaucoma 1, open angle, F",
+BMGC_DS12163,BMG_DS040860,,,,,,,,,C1863958,,603376,MONDO:0011310,"long chain fatty acids, defect in transport of",
+BMGC_DS12164,BMG_DS040861,,"Hyperthyroidism, Familial Gestational",,,,,,,C1863959,C566384,603373,MONDO:0011309,familial gestational hyperthyroidism,
+BMGC_DS12165,BMG_DS040864,703388005,Finnish lethal neonatal metabolic syndrome,,,,,DOID:0111455,GRACILE syndrome,C1864002,C537934,603358,MONDO:0011308,GRACILE syndrome,"Growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death | Fellman syndrome | Finnish lethal neonatal metabolic syndrome | GRACILE syndrome | Finnish lactic acidosis with hepatic hemosiderosis | Growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death (disorder)"
+BMGC_DS12166,BMG_DS040865,,SCHIZOPHRENIA 2,,,,,DOID:0070078,schizophrenia 2,C1864010,,603342,MONDO:0011307,schizophrenia 2,
+BMGC_DS12167,BMG_DS040867,,Cerebral Cavernous Malformations 3,,,,,,,C1864040,C566393,603285,MONDO:0011305,cerebral cavernous malformation 3,
+BMGC_DS12168,BMG_DS040868,,CEREBRAL CAVERNOUS MALFORMATIONS 2,,,,,,,C1864041,,603284;607929,MONDO:0011304,cerebral cavernous malformation 2,
+BMGC_DS12169,BMG_DS040869,,"DIABETES MELLITUS, INSULIN-DEPENDENT, 17",,,,,,,C1864068,,603266,MONDO:0011302,type 1 diabetes mellitus 17,
+BMGC_DS12170,BMG_DS040870,,"PSEUDOHYPOPARATHYROIDISM, TYPE IB",,,,,DOID:0080222,pseudohypoparathyroidism type 1B,C1864100,,603233;610540;139320;603666,MONDO:0011301,pseudohypoparathyroidism type 1B,
+BMGC_DS12171,BMG_DS040871,,Myopia 3,,,,,,,C1864111,C566397,603221,MONDO:0011300,"myopia 3, autosomal dominant",
+BMGC_DS12172,BMG_DS040872,,HUNTINGTON DISEASE-LIKE 1,,,,,,,C1864112,,603218;176640,MONDO:0011299,Huntington disease-like 1,
+BMGC_DS12173,BMG_DS040874,,"Epilepsy, Nocturnal Frontal Lobe, Type 2",,,,,,,C1864125,C566400,603204,MONDO:0011297,autosomal dominant nocturnal frontal lobe epilepsy 2,
+BMGC_DS12174,BMG_DS040875,,"MECKEL SYNDROME, TYPE 2",,,,,,,C1864148,,603194;613277,MONDO:0011296,"Meckel syndrome, type 2",
+BMGC_DS12175,BMG_DS040878,,"Dermatitis, Atopic, 1",,,,,,,C1864155,C566404,,,,
+BMGC_DS12176,BMG_DS040884,,CDAGS SYNDROME,,,,,,,C1864186,,603116;620204,MONDO:0011287,craniosynostosis-anal anomalies-porokeratosis syndrome,
+BMGC_DS12177,BMG_DS040885,,"DEAFNESS, AUTOSOMAL RECESSIVE 13",,,,,,,C1864199,,603098,MONDO:0011286,autosomal recessive nonsyndromic hearing loss 13,
+BMGC_DS12178,BMG_DS040886,,"Macular Degeneration, Age-Related, 1",,,,,,,C1864205,C566411,603075,MONDO:0011285,age related macular degeneration 1,
+BMGC_DS12179,BMG_DS040888,,Endplate Acetylcholinesterase Deficiency,,,,,,,C1864233,C566415,603034,MONDO:0011281,congenital myasthenic syndrome 5,
+BMGC_DS12180,BMG_DS040890,,SCHIZOPHRENIA 6,,,,,DOID:0070082,schizophrenia 6,C1864275,,603013,MONDO:0011280,schizophrenia 6,
+BMGC_DS12181,BMG_DS040891,,"Deafness, Autosomal Recessive 17",,,,,,,C1864276,C566418,603010,MONDO:0011279,autosomal recessive nonsyndromic hearing loss 17,
+BMGC_DS12182,BMG_DS040893,,"ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE",,,,,,,C1864356,,602875,MONDO:0011275,"acromesomelic dysplasia 1, Maroteaux type",
+BMGC_DS12183,BMG_DS040894,,PREMATURE CHROMATID SEPARATION TRAIT,,,,,,,C1864389,,602860;176430,MONDO:0008304,premature chromatid separation trait,
+BMGC_DS12184,BMG_DS040895,,"Peroxisome Biogenesis Disorder, Complementation Group 7",,,,,,,C1864399,C566422,,,,
+BMGC_DS12185,BMG_DS040896,,Muenke Syndrome,,,,,DOID:0060703,Muenke Syndrome,C1864436,C537369,602849,MONDO:0011274,Muenke syndrome,
+BMGC_DS12186,BMG_DS040897,,Histiocytosis with joint contractures and sensorineural deafness,,,,,,,C1864445,C538322,602782,MONDO:0011273,H syndrome,
+BMGC_DS12187,BMG_DS040898,,Retinitis Pigmentosa 25,,,,,DOID:0110384,retinitis pigmentosa 25,C1864446,C566425,602772,MONDO:0011272,retinitis pigmentosa 25,
+BMGC_DS12188,BMG_DS040900,,PSORIASIS 2,,,,,DOID:0080475,psoriasis 2,C1864497,,602723;607211,MONDO:0011269,psoriasis 2,
+BMGC_DS12189,BMG_DS040901,,,,,,,,,C1864498,,,MONDO:0018440,autosomal recessive distal renal tubular acidosis,
+BMGC_DS12190,BMG_DS040904,,"Cataract, posterior polar, 4",,,,,,,C1864567,C535344,610623,MONDO:0012527,cataract 11 multiple types,
+BMGC_DS12191,BMG_DS040905,,RETINITIS PIGMENTOSA 36,,,,,,,C1864621,,610598;610599,MONDO:0012523,retinitis pigmentosa 36,
+BMGC_DS12192,BMG_DS040906,,"Diabetes Mellitus, Transient Neonatal, 3",,,,,,,C1864623,C566432,610582,MONDO:0012522,"diabetes mellitus, transient neonatal, 3",
+BMGC_DS12193,BMG_DS040907,,"CHROMOSOME 16p13.3 DELETION SYNDROME, PROXIMAL",,,,,,,C1864648,,610543,MONDO:0012519,Rubinstein-Taybi syndrome due to 16p13.3 microdeletion,
+BMGC_DS12194,BMG_DS040909,,"GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY",,,,,,,C1864651,,176801;610539,MONDO:0012517,Gaucher disease due to saposin C deficiency,
+BMGC_DS12195,BMG_DS040910,,"Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate",,,,,,,C1864652,C537405,610536,MONDO:0012516,mandibulofacial dysostosis-microcephaly syndrome,
+BMGC_DS12196,BMG_DS040911,,"Glaucoma 1, Open Angle, M",,,,,,,C1864653,C566436,610535,MONDO:0012515,"glaucoma 1, open angle, M",
+BMGC_DS12197,BMG_DS040912,,,,,,,,,C1864663,,610532,MONDO:0012514,hypomyelinating leukodystrophy 5,
+BMGC_DS12198,BMG_DS040913,,"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4",,,,,,,C1864668,C566437,610131,MONDO:0012415,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4",
+BMGC_DS12199,BMG_DS040914,,NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCY,,,,,,,C1864669,,610127,MONDO:0012414,neuronal ceroid lipofuscinosis 10,
+BMGC_DS12200,BMG_DS040915,,"Neuronal Ceroid Lipofuscinosis, Congenital",,,,,,,C1864670,C566438,,MONDO:0850001,congenital neuronal ceroid lipofuscinosis,
+BMGC_DS12201,BMG_DS040916,,"Microphthalmia, Syndromic 6",,,,,DOID:0111805,syndromic microphthalmia 6,C1864689,C566440,607932,MONDO:0011936,microphthalmia with brain and digit anomalies,
+BMGC_DS12202,BMG_DS040917,,"Microphthalmia, Syndromic 5",,,,,DOID:0111806,syndromic microphthalmia 5,C1864690,C566441,610125,MONDO:0012413,syndromic microphthalmia type 5,
+BMGC_DS12203,BMG_DS040918,,Complement Component 7 Deficiency,,,,,DOID:0060300,complement component 7 deficiency,C1864694,C566443,610102,MONDO:0012412,complement component 7 deficiency,
+BMGC_DS12204,BMG_DS040919,,"Giant Axonal Neuropathy, Autosomal Dominant",,,,,,,C1864695,C566444,610100,MONDO:0012411,giant axonal neuropathy 2,
+BMGC_DS12205,BMG_DS040920,,"Myopathy, Distal 3",,,,,,,C1864706,C566445,610099,MONDO:0012410,Finnish upper limb-onset distal myopathy,
+BMGC_DS12206,BMG_DS040921,,"MICROPHTHALMIA, ISOLATED 2",,,,,,,C1864720,,610093;142993,MONDO:0012409,isolated microphthalmia 2,
+BMGC_DS12207,BMG_DS040922,,"Microphthalmia, Isolated, with Coloboma 3",,,,,,,C1864721,C566447,610092,MONDO:0012408,"microphthalmia, isolated, with coloboma 3",
+BMGC_DS12208,BMG_DS040923,,"Microphthalmia, Cataracts, and Iris Abnormalities",,,,,,,C1864722,C566448,,,,
+BMGC_DS12209,BMG_DS040924,,Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency,,,,,DOID:0111329,pyridoxamine 5'-phosphate oxidase deficiency,C1864723,C566449,610090,MONDO:0012407,pyridoxal phosphate-responsive seizures,
+BMGC_DS12210,BMG_DS040926,,"Polyposis Syndrome, Hereditary Mixed, 2",,,,,,,C1864730,C566451,610069,MONDO:0012405,"polyposis syndrome, hereditary mixed, 2",
+BMGC_DS12211,BMG_DS040929,,,,,,,,,C1864733,,610064,MONDO:0012402,"opioid dependence, susceptibility to, 1",
+BMGC_DS12212,BMG_DS040930,,"Corneal Dystrophy, Congenital Stromal",,,,,DOID:0060445,congenital stromal corneal dystrophy,C1864738,C566452,610048,MONDO:0012401,congenital stromal corneal dystrophy,
+BMGC_DS12213,BMG_DS040931,,"Deafness, Autosomal Recessive 53",,,,,,,C1864746,C566453,609706,MONDO:0012333,autosomal recessive nonsyndromic hearing loss 53,
+BMGC_DS12214,BMG_DS040935,,Short Stature And Facioauriculothoracic Malformations,,,,,,,C1864791,C566457,609654,MONDO:0012329,short stature and Facioauriculothoracic malformations,
+BMGC_DS12215,BMG_DS040936,,TRICHILEMMAL CYST 1,,,,,,,C1864801,,609649,,,
+BMGC_DS12216,BMG_DS040937,,"Deafness, Autosomal Recessive 46",,,,,,,C1864815,C566459,609647,MONDO:0012327,autosomal recessive nonsyndromic hearing loss 46,
+BMGC_DS12217,BMG_DS040938,,"Deafness, Autosomal Recessive 42",,,,,,,C1864818,C566460,609646,MONDO:0012326,autosomal recessive nonsyndromic hearing loss 42,
+BMGC_DS12218,BMG_DS040940,,Frias syndrome,,,,,,,C1864825,C535639,609640,MONDO:0012324,Frias syndrome,
+BMGC_DS12219,BMG_DS040941,,"Epidermolysis bullosa, lethal acantholytic",,,,,,,C1864826,C535493,609638,MONDO:0012323,lethal acantholytic epidermolysis bullosa,
+BMGC_DS12220,BMG_DS040942,,HOLOPROSENCEPHALY 5,,,,,,,C1864827,,609637;603073,MONDO:0012322,holoprosencephaly 5,
+BMGC_DS12221,BMG_DS040943,,ALZHEIMER DISEASE 10,,,,,,,C1864828,,609636,MONDO:0012321,Alzheimer disease 10,
+BMGC_DS12222,BMG_DS040944,,,,,,,,,C1864839,,610508,MONDO:0012513,maturity-onset diabetes of the young type 7,
+BMGC_DS12223,BMG_DS040945,,Combined Oxidative Phosphorylation Deficiency 3,,,,,DOID:0111486,combined oxidative phosphorylation deficiency 3,C1864840,C566467,610505,MONDO:0012512,fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3,
+BMGC_DS12224,BMG_DS040946,,Combined Oxidative Phosphorylation Deficiency 2,,,,,DOID:0111483,combined oxidative phosphorylation deficiency 2,C1864843,C566468,610498,MONDO:0012510,combined oxidative phosphorylation defect type 2,
+BMGC_DS12225,BMG_DS040947,,"Pigmented Nodular Adrenocortical Disease, Primary, 1",,,,,DOID:0070546,primary pigmented nodular adrenocortical disease 1,C1864846,C566469,610489,MONDO:0012509,"pigmented nodular adrenocortical disease, primary, 1",
+BMGC_DS12226,BMG_DS040949,,RETINAL CONE DYSTROPHY 4,,,,,,,C1864849,,608171;610478,MONDO:0012507,retinal cone dystrophy 4,
+BMGC_DS12227,BMG_DS040950,,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 11",,,,,,,C1864850,C566471,610476,MONDO:0012506,arrhythmogenic right ventricular dysplasia 11,
+BMGC_DS12228,BMG_DS040951,,"Pigmented Nodular Adrenocortical Disease, Primary, 2",,,,,DOID:0070547,primary pigmented nodular adrenocortical disease 2,C1864851,C566472,610475,MONDO:0012505,"pigmented nodular adrenocortical disease, primary, 2",
+BMGC_DS12229,BMG_DS040952,,CATSHL syndrome,,,,,DOID:0111160,camptodactyly-tall stature-scoliosis-hearing loss syndrome,C1864852,C537975,610474,MONDO:0012504,camptodactyly-tall stature-scoliosis-hearing loss syndrome,
+BMGC_DS12230,BMG_DS040953,,"Tumoral Calcinosis, Normophosphatemic, Familial",,,,,,,C1864861,C566473,610455,MONDO:0012502,normophosphatemic familial tumoral calcinosis,
+BMGC_DS12231,BMG_DS040954,,,,,,,,,C1864868,,610446,MONDO:0012499,"Buruli ulcer, susceptibility to",
+BMGC_DS12232,BMG_DS040955,,"Night Blindness, Congenital Stationary, Autosomal Dominant 1",,,,,,,C1864869,C566474,610445,MONDO:0012498,congenital stationary night blindness autosomal dominant 1,
+BMGC_DS12233,BMG_DS040956,,"Night Blindness, Congenital Stationary, Autosomal Dominant 3",,,,,,,C1864870,C566475,610444,MONDO:0012497,congenital stationary night blindness autosomal dominant 3,
+BMGC_DS12234,BMG_DS040957,,Chromosome 17q21.31 Deletion Syndrome,,,,,,,C1864871,C566476,610443,MONDO:0018216;MONDO:0012496,Koolen-de Vries syndrome | Koolen-de Vries syndrome due to 17q21.31 microdeletion syndrome,
+BMGC_DS12235,BMG_DS040958,,"Spondyloepimetaphyseal dysplasia, Genevieve type",,,,,DOID:0080576,"spondyloepimetaphyseal dysplasia, Genevieve-type",C1864872,C535785,610442,MONDO:0012495,"spondyloepimetaphyseal dysplasia, Genevieve type",
+BMGC_DS12236,BMG_DS040959,,Testicular Microlithiasis,,,,,,,C1864873,C566478,610441,MONDO:0012494,testicular microlithiasis,
+BMGC_DS12237,BMG_DS040963,,"Night Blindness, Congenital Stationary, Type 2B",,,,,,,C1864877,C536122,,,,
+BMGC_DS12238,BMG_DS040966,,,,,,,,,C1864880,,610424,MONDO:0012488,"hepatitis B virus, susceptibility to",
+BMGC_DS12239,BMG_DS040967,,Retinal Cone Dystrophy 3A,,,,,DOID:0081025,retinal cone dystrophy 3A,C1864900,C566483,610024,MONDO:0012398,retinal cone dystrophy 3A,
+BMGC_DS12240,BMG_DS040968,,"Brachydactyly, Coloboma, And Anterior Segment Dysgenesis",,,,,,,C1864901,C566484,610023,MONDO:0012397,"brachydactyly, coloboma, and anterior segment dysgenesis",
+BMGC_DS12241,BMG_DS040969,,"Hyperinsulinemic hypoglycemia, familial, 7",,,,,DOID:0070214,familial hyperinsulinemic hypoglycemia 7,C1864902,C538376,610021,MONDO:0012396,exercise-induced hyperinsulinism,
+BMGC_DS12242,BMG_DS040970,,Hyperinsulinemic hypoglycemia,,,,,,,C1864903,,MTHU000368,MONDO:0005803,hyperinsulinemic hypoglycemia,
+BMGC_DS12243,BMG_DS040971,,"Cataract, autosomal recessive congenital 2",,,,,,,C1864908,C535337,610019,MONDO:0012395,cataract 18,
+BMGC_DS12244,BMG_DS040972,,"Glutamine deficiency, congenital",,,,,,,C1864910,C536832,610015,MONDO:0012393,congenital brain dysgenesis due to glutamine synthetase deficiency,
+BMGC_DS12245,BMG_DS040973,,2-Methylbutyryl-CoA Dehydrogenase Deficiency,,,,,,,C1864912,C566487,610006,MONDO:0012392,2-methylbutyryl-CoA dehydrogenase deficiency,
+BMGC_DS12246,BMG_DS040974,,Northern epilepsy syndrome,,,,,,,C1864923,C537952,610003,MONDO:0012391,neuronal ceroid lipofuscinosis 8 northern epilepsy variant,
+BMGC_DS12247,BMG_DS040979,,Osteosclerosis with ichthyosis and premature ovarian failure,,,,,,,C1864942,C536064,609993,MONDO:0012387,osteosclerosis-ichthyosis-premature ovarian failure syndrome,
+BMGC_DS12248,BMG_DS040983,,"Natural Killer Cell Deficiency, Familial Isolated",,,,,DOID:0111967,immunodeficiency 54,C1864947,C566492,609981,MONDO:0012383,primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency,
+BMGC_DS12249,BMG_DS040984,,"Hyperinsulinemic Hypoglycemia, Familial, 4",,,,,,,C1864948,C566493,609975,MONDO:0012382,"hyperinsulinemic hypoglycemia, familial, 4",
+BMGC_DS12250,BMG_DS040985,,"Hyperinsulinemic Hypoglycemia, Familial, 5",,,,,,,C1864952,C566494,609968,MONDO:0012381,hyperinsulinism due to INSR deficiency,
+BMGC_DS12251,BMG_DS040986,,"Deafness, Autosomal Dominant 53",,,,,,,C1864957,C566495,609965,MONDO:0012380,autosomal dominant nonsyndromic hearing loss 53,
+BMGC_DS12252,BMG_DS040990,,"DEAFNESS, AUTOSOMAL RECESSIVE 55",,,,,,,C1864962,,609952,MONDO:0012376,autosomal recessive nonsyndromic hearing loss 55,
+BMGC_DS12253,BMG_DS040991,,"Deafness, Autosomal Recessive 47",,,,,,,C1864964,C566498,609946,MONDO:0012375,autosomal recessive nonsyndromic hearing loss 47,
+BMGC_DS12254,BMG_DS040992,,"Brachyphalangy, polydactyly, and tibial aplasia-hypoplasia",,,,,,,C1864965,C537100,609945,MONDO:0012374,"brachyphalangy, polydactyly, and tibial aplasia/hypoplasia",
+BMGC_DS12255,BMG_DS040993,,"Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features",,,,,,,C1864966,C536182,609944,MONDO:0012373,"ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features",
+BMGC_DS12256,BMG_DS040994,,"DEAFNESS, AUTOSOMAL RECESSIVE 51",,,,,,,C1864968,,609941,MONDO:0012370,autosomal recessive nonsyndromic hearing loss 51,
+BMGC_DS12257,BMG_DS040996,,"Migraine, Familial Hemiplegic, 3",,,,,,,C1864987,C566500,609634,MONDO:0012320,"migraine, familial hemiplegic, 3",
+BMGC_DS12258,BMG_DS040999,,"Visceral Neuropathy, Familial, Autosomal Dominant",,,,,,,C1864996,C566502,609629,MONDO:0012317,"visceral neuropathy, familial, 3, autosomal dominant",
+BMGC_DS12259,BMG_DS041000,703540008,Majeed syndrome,,,,M04.8,,,C1864997,C537839,609628,MONDO:0012316,Majeed syndrome,"Majeed syndrome | Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis (disorder) | Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anaemia and neutrophilic dermatosis | Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis"
+BMGC_DS12260,BMG_DS041001,,Short QT Syndrome 3,,,,,,,C1865018,C566504,609622,MONDO:0012314,short QT syndrome type 3,
+BMGC_DS12261,BMG_DS041002,,Short QT Syndrome 2,,,,,,,C1865019,C566505,609621,MONDO:0012313,short QT syndrome type 2,
+BMGC_DS12262,BMG_DS041003,,Short QT Syndrome 1,,,,,,,C1865020,C566506,609620,MONDO:0012312,short QT syndrome type 1,
+BMGC_DS12263,BMG_DS041004,,"Spondylomegaepiphyseal Dysplasia With Upper Limb Mesomelia, Punctate Calcifications, And Deafness",,,,,,,C1865022,C566507,609616,MONDO:0012311,"spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctate calcifications, and deafness",
+BMGC_DS12264,BMG_DS041005,,"fibrosis of extraocular muscles, congenital, with synergistic divergence",,,,,,,C1865040,C566508,609612,MONDO:0012310,"fibrosis of extraocular muscles, congenital, with synergistic divergence",
+BMGC_DS12265,BMG_DS041007,,PARIETAL FORAMINA 2,,,,,,,C1865044,,605420;609597,MONDO:0012309,parietal foramina 2,
+BMGC_DS12266,BMG_DS041008,,"SCAPHOCEPHALY, MAXILLARY RETRUSION, AND IMPAIRED INTELLECTUAL DEVELOPMENT",,,,,,,C1865070,,176943;609579,MONDO:0012307,"familial scaphocephaly syndrome, McGillivray type",
+BMGC_DS12267,BMG_DS041010,,"Tooth Agenesis, Selective, 2",,,,,,,C1865092,C566513,602639,MONDO:0011265,"tooth agenesis, selective, 2",
+BMGC_DS12268,BMG_DS041011,,"Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal",,,,,,,C1865117,C566514,602613,MONDO:0011263,"skeletal dysplasia and progressive central nervous system degeneration, lethal",
+BMGC_DS12269,BMG_DS041015,,BRANCHIOOTIC SYNDROME 1,,,,,,,C1865143,,601653;602588,MONDO:0011258,branchiootic syndrome 1,
+BMGC_DS12270,BMG_DS041016,,Congenital disorder of glycosylation type 1B,,,,,,,C1865145,C535740,602579,MONDO:0011257,MPI-congenital disorder of glycosylation,
+BMGC_DS12271,BMG_DS041018,,Mandibulofacial Dysostosis with Macroblepharon and Macrostomia,,,,,,,C1865181,C566520,602562,MONDO:0011255,mandibulofacial dysostosis-macroblepharon-macrostomia syndrome,
+BMGC_DS12272,BMG_DS041021,,"Spondyloepimetaphyseal Dysplasia, Shohat Type",,,,,,,C1865185,C566523,602557,MONDO:0011252,"spondyloepimetaphyseal dysplasia, Shohat type",
+BMGC_DS12273,BMG_DS041024,,Torsion dystonia with onset in infancy,,,,,DOID:0090058,torsion dystonia with onset in infancy,C1865205,C536969,602554,MONDO:0011249,torsion dystonia with onset in infancy,
+BMGC_DS12274,BMG_DS041027,,"Muscular Dystrophy, Congenital, Megaconial Type",,,,,,,C1865233,C566527,602541,MONDO:0011246,megaconial type congenital muscular dystrophy,
+BMGC_DS12275,BMG_DS041028,,"ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS",,,,,,,C1865234,,602540,MONDO:0011245,"ichthyosis, hystrix-like, with hearing loss",
+BMGC_DS12276,BMG_DS041029,,"Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly",,,,,,,C1865267,C566529,602531,MONDO:0011243,grange syndrome,
+BMGC_DS12277,BMG_DS041030,,,,,,,,,C1865270,,602522,MONDO:0011242,Bartter disease type 4A,
+BMGC_DS12278,BMG_DS041032,,Megalencephaly cutis marmorata telangiectatica congenita,,,,,,,C1865285,C536142,602501,MONDO:0011240,megalencephaly-capillary malformation-polymicrogyria syndrome,
+BMGC_DS12279,BMG_DS041033,,"MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA",,,,,,,C1865286,,602499,MONDO:0011239,colobomatous macrophthalmia-microcornea syndrome,
+BMGC_DS12280,BMG_DS041034,,"HYPERLIPIDEMIA, COMBINED, 1",,,,,,,C1865289,,602491,MONDO:0011237,"hyperlipidemia, combined, 1",
+BMGC_DS12281,BMG_DS041035,,"Hyperinsulinemic hypoglycemia, familial, 3",,,,,,,C1865290,C538374,602485,MONDO:0011236,hyperinsulinism due to glucokinase deficiency,
+BMGC_DS12282,BMG_DS041037,,Pelvic dysplasia arthrogryposis of lower limbs,,,,,,,C1865294,C535548,602484,MONDO:0011235,pelvic dysplasia-arthrogryposis of lower limbs syndrome,
+BMGC_DS12283,BMG_DS041038,702443003,Auriculo-condylar syndrome,,,,,,,C1865295,C538270,,MONDO:0000107,auriculocondylar syndrome,Auriculo-condylar syndrome | Question-mark ear syndrome | Auriculo-condylar syndrome (disorder) | Auriculocondylar syndrome | Dysgnathia complex
+BMGC_DS12284,BMG_DS041039,,"MIGRAINE, FAMILIAL HEMIPLEGIC, 2",,,,,DOID:0111182,familial hemiplegic migraine 2,C1865322,,182340;602481,MONDO:0011232,"migraine, familial hemiplegic, 2",
+BMGC_DS12285,BMG_DS041040,,"Migraine, Familial Basilar",,,,,,,C1865323,C566540,,,,
+BMGC_DS12286,BMG_DS041041,,"Febrile Convulsions, Familial, 2",,,,,,,C1865342,C566541,,MONDO:0011231,"febrile seizures, familial, 2",
+BMGC_DS12287,BMG_DS041042,,OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE,,,,,DOID:0060887,ossification of the posterior longitudinal ligament of spine,C1865343,,602475,MONDO:0011230,ossification of the posterior longitudinal ligament of the spine,
+BMGC_DS12288,BMG_DS041043,811000124106;723307008,Ethylmalonic encephalopathy,,,,,DOID:0060640,ethylmalonic encephalopathy,C1865349,C535737,602473,MONDO:0011229,ethylmalonic encephalopathy,Ethylmalonic encephalopathy (disorder) | Ethylmalonic encephalopathy
+BMGC_DS12289,BMG_DS041045,,,,,,,,,C1865361,,602471,MONDO:0011227,short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome,
+BMGC_DS12290,BMG_DS041046,,"Deafness, Autosomal Dominant 15",,,,,,,C1865366,C566545,602459,MONDO:0011226,autosomal dominant nonsyndromic hearing loss 15,
+BMGC_DS12291,BMG_DS041047,,Severe combined immunodeficiency with sensitivity to ionizing radiation,,,,,DOID:0090012,severe combined immunodeficiency with sensitivity to ionizing radiation,C1865370,C537589,602450,MONDO:0011225,severe combined immunodeficiency due to DCLRE1C deficiency,
+BMGC_DS12292,BMG_DS041048,,"SEVERE COMBINED IMMUNODEFICIENCY, ATHABASKAN-TYPE",,,,,,,C1865371,,602450,,,
+BMGC_DS12293,BMG_DS041049,,"SEVERE COMBINED IMMUNODEFICIENCY, PARTIAL",,,,,,,C1865373,,602450;605988,,,
+BMGC_DS12294,BMG_DS041050,,"Amyotrophy, monomelic",,,,,,,C1865384,C538253,602440,MONDO:0011224,monomelic amyotrophy,
+BMGC_DS12295,BMG_DS041051,,"Amyotrophic Lateral Sclerosis 4, Juvenile",,,,,,,C1865409,C566550,602433,MONDO:0011223,amyotrophic lateral sclerosis type 4,
+BMGC_DS12296,BMG_DS041053,,,,,,,,,C1865433,,,MONDO:0018801,congenital bilateral absence of vas deferens,
+BMGC_DS12297,BMG_DS041054,,Weyers ulnar ray-oligodactyly syndrome,,,,,,,C1865566,C536696,602418,MONDO:0011221,Weyers ulnar ray/oligodactyly syndrome,
+BMGC_DS12298,BMG_DS041057,709490002,Desmosterolosis,,,,,,,C1865596,C566555,602398,MONDO:0011217,desmosterolosis,Desmosterolosis (disorder) | Desmosterolosis
+BMGC_DS12299,BMG_DS041058,,"HEMOCHROMATOSIS, TYPE 2A",,,,,DOID:0111027,hemochromatosis type 2A,C1865614,,608374;602390,MONDO:0011216,hemochromatosis type 2A,
+BMGC_DS12300,BMG_DS041059,,"HEMOCHROMATOSIS, TYPE 2B",,,,,DOID:0111032,hemochromatosis type 2B,C1865616,,606464;613313,MONDO:0013220,hemochromatosis type 2B,
+BMGC_DS12301,BMG_DS041060,722109008,Gracile bone dysplasia,,,,,,,C1865639,C537291,602361,MONDO:0011215,osteocraniostenosis,Osteocraniostenosis (disorder) | Osteocraniostenosis | Gracile bone dysplasia | Osteocraniosplenic syndrome
+BMGC_DS12302,BMG_DS041061,,"Cholestasis, progressive familial intrahepatic 3",,,,,DOID:0070223,progressive familial intrahepatic cholestasis 3,C1865643,C535935,602347,MONDO:0011214,progressive familial intrahepatic cholestasis type 3,
+BMGC_DS12303,BMG_DS041062,,"Plantar Lipomatosis, Unusual Facies, and Developmental Delay",,,,,,,C1865644,C566559,602342,MONDO:0011213,Pierpont syndrome,
+BMGC_DS12304,BMG_DS041064,,"Spondylometaphyseal dysplasia, axial",,,,,DOID:0112299,axial spondylometaphyseal dysplasia,C1865695,C535795,602271,MONDO:0011211,axial spondylometaphyseal dysplasia,
+BMGC_DS12305,BMG_DS041067,,"XANTHOMATOSIS, SUSCEPTIBILITY TO",,,,,,,C1865704,,602247,MONDO:0011207,"xanthomatosis, susceptibility to",
+BMGC_DS12306,BMG_DS041068,,Ventriculomegaly With Defects Of The Radius And Kidney,,,,,,,C1865780,C566565,602200,MONDO:0011206,ventriculomegaly with defects of the radius and kidney,
+BMGC_DS12307,BMG_DS041069,,Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency,,,,,,,C1865781,C566566,602199,MONDO:0011205,medium chain 3-ketoacyl-Coa thiolase deficiency,
+BMGC_DS12308,BMG_DS041070,,Pierre Robin sequence with pectus excavatum and rib and scapular anomalies,,,,,,,C1865783,C535775,602196,MONDO:0011203,Pierre Robin sequence with pectus excavatum and rib and scapular anomalies,
+BMGC_DS12309,BMG_DS041071,723999009,RHYNS syndrome,,,,,,,C1865794,C537612,602152,MONDO:0011202,RHYNS syndrome,"Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder) | RHYNS syndrome | Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome | RHYNS (retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia) syndrome"
+BMGC_DS12310,BMG_DS041074,,"TREMOR, HEREDITARY ESSENTIAL, 2",,,,,DOID:0111429,essential tremor 2,C1865810,,602134,MONDO:0011201,"tremor, hereditary essential, 2",
+BMGC_DS12311,BMG_DS041075,,Torsion dystonia 7,,,,,,,C1865818,C566572,602124,MONDO:0011200,torsion dystonia 7,
+BMGC_DS12312,BMG_DS041076,,"CERVICAL DYSTONIA, PRIMARY",,,,,DOID:0090040,torsion dystonia 7,C1865819,,602124,,,
+BMGC_DS12313,BMG_DS041077,,"Nephropathy, Progressive Tubulointerstitial, with Cholestatic Liver Disease",,,,,,,C1865831,C566573,602114,MONDO:0011199,"nephropathy, progressive tubulointerstitial, with cholestatic liver disease",
+BMGC_DS12314,BMG_DS041078,,"Spondyloepimetaphyseal Dysplasia, Missouri Type",,,,,DOID:0080030,"spondyloepimetaphyseal dysplasia, Missouri type",C1865832,C566574,602111,MONDO:0011198,"spondyloepimetaphyseal dysplasia, Missouri type",
+BMGC_DS12315,BMG_DS041080,,,,,,,,,C1865864,,602099,MONDO:0011196,amyotrophic lateral sclerosis type 5,
+BMGC_DS12316,BMG_DS041081,,"Usher Syndrome, Type IE",,,,,,,C1865865,C566577,602097,MONDO:0011195,Usher syndrome type 1E,
+BMGC_DS12317,BMG_DS041082,700453005,Congenital sensorineural hearing loss,,,,,,,C1865866,,MTHU013508,,,Congenital sensorineural hearing loss (disorder) | Congenital sensorineural hearing loss | Congenital sensorineural deafness
+BMGC_DS12318,BMG_DS041083,,ALZHEIMER DISEASE 5,,,,,,,C1865868,,602096,MONDO:0011194,Alzheimer disease 5,
+BMGC_DS12319,BMG_DS041084,,Cone Dystrophy 3,,,,,DOID:0080314,cone-rod dystrophy 14,C1865869,C566579,602093,MONDO:0011193,cone dystrophy 3,
+BMGC_DS12320,BMG_DS041085,,"Deafness, Autosomal Recessive 18",,,,,,,C1865870,C566580,602092,MONDO:0011192,autosomal recessive nonsyndromic hearing loss 18A,
+BMGC_DS12321,BMG_DS041086,,"HEMANGIOMA, CAPILLARY INFANTILE",,,,,,,C1865871,,602089,MONDO:0011191,capillary infantile hemangioma,
+BMGC_DS12322,BMG_DS041087,,NEPHRONOPHTHISIS 2,,,,,,,C1865872,,243305;602088,MONDO:0011190,nephronophthisis 2,
+BMGC_DS12323,BMG_DS041088,,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 4",,,,,,,C1865881,C566583,602087,MONDO:0011189,arrhythmogenic right ventricular dysplasia 4,
+BMGC_DS12324,BMG_DS041089,,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 3",,,,,,,C1865882,C566584,602086,MONDO:0011188,arrhythmogenic right ventricular dysplasia 3,
+BMGC_DS12325,BMG_DS041090,,"Polydactyly, Postaxial, Type A2",,,,,,,C1865883,C566585,602085,MONDO:0011187,"polydactyly, postaxial, type A2",
+BMGC_DS12326,BMG_DS041091,,"Usher Syndrome, Type IF",,,,,,,C1865885,C566586,602083,MONDO:0011186,Usher syndrome type 1F,
+BMGC_DS12327,BMG_DS041092,,"FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2",,,,,DOID:0081016,congenital fibrosis of the extraocular muscles 2,C1865915,,602078;602753,MONDO:0011181,"fibrosis of extraocular muscles, congenital, 2",
+BMGC_DS12328,BMG_DS041093,,Bilateral ptosis,,,,,,,C1865916,,MTHU005602,,,
+BMGC_DS12329,BMG_DS041094,,"Broad Terminal Phalanges, Familial",,,,,,,C1865923,C566588,602071,MONDO:0011180,"broad terminal phalanges, familial",
+BMGC_DS12330,BMG_DS041095,,"Infantile convulsions and paroxysmal choreoathetosis, familial",,,,,,,C1865926,C535522,602066,MONDO:0011178,infantile convulsions and choreoathetosis,
+BMGC_DS12331,BMG_DS041096,,,,,,,DOID:0111655,pure hair and nail ectodermal dysplasia,C1865951,,,,,
+BMGC_DS12332,BMG_DS041097,,"Hypomagnesemia 1, Intestinal",,,,,,,C1865974,C566593,602014,MONDO:0011176,intestinal hypomagnesemia 1,
+BMGC_DS12333,BMG_DS041098,,FRIEDREICH ATAXIA 2,,,,,,,C1865981,,601992,MONDO:0011175,Friedreich ataxia 2,
+BMGC_DS12334,BMG_DS041099,,Hyperzincemia with Functional Zinc Depletion,,,,,,,C1865986,C566595,601979,MONDO:0011174,hyperzincemia with functional zinc depletion,
+BMGC_DS12335,BMG_DS041101,,Odontotrichoungual-Digital-Palmar Syndrome,,,,,,,C1865998,C566598,601957,MONDO:0011171,odonto-tricho-ungual-digito-palmar syndrome,
+BMGC_DS12336,BMG_DS041102,,"Muscular Dystrophy, Limb-Girdle, Type 2G",,,,,,,C1866008,C566599,601954,MONDO:0011170,autosomal recessive limb-girdle muscular dystrophy type 2G,
+BMGC_DS12337,BMG_DS041103,,Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma,,,,,,,C1866029,C566600,601952,MONDO:0011169,keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome,
+BMGC_DS12338,BMG_DS041104,,"EPISODIC ATAXIA, TYPE 5",,,,,DOID:0050993,episodic ataxia type 5,C1866039,,601949;613855,MONDO:0013464,episodic ataxia type 5,
+BMGC_DS12339,BMG_DS041105,,"DIABETES MELLITUS, INSULIN-DEPENDENT, 10",,,,,,,C1866040,,601942,MONDO:0011168,type 1 diabetes mellitus 10,
+BMGC_DS12340,BMG_DS041106,,"DIABETES MELLITUS, INSULIN-DEPENDENT, 6",,,,,,,C1866041,,601941,MONDO:0011167,type 1 diabetes mellitus 6,
+BMGC_DS12341,BMG_DS041107,,Severe hydrops,,,,,,,C1866048,,MTHU041796,,,
+BMGC_DS12342,BMG_DS041108,,"Deafness, Congenital Heart Defects, and Posterior Embryotoxon",,,,,,,C1866053,C566604,617992,MONDO:0060713,"deafness, congenital heart defects, and posterior embryotoxon",
+BMGC_DS12343,BMG_DS041109,,,,,,,,,C1866070,,613705,MONDO:0013378,orofacial cleft 10,
+BMGC_DS12344,BMG_DS041110,,,,,,,,,C1866075,,601894,MONDO:0011165,glomerulopathy with fibronectin deposits 2,
+BMGC_DS12345,BMG_DS041112,,,,,,,,,C1866077,,601887,MONDO:0011163,"malignant hyperthermia, susceptibility to, 5",
+BMGC_DS12346,BMG_DS041113,,"Cataract, Zonular Pulverulent 3",,,,,,,C1866078,C566608,601885,MONDO:0011162,cataract 14 multiple types,
+BMGC_DS12347,BMG_DS041114,,Left-Right Axis Malformations,,,,,,,C1866091,C566610,,,,
+BMGC_DS12348,BMG_DS041115,,"DEAFNESS, AUTOSOMAL RECESSIVE 15",,,,,,,C1866094,,601869;608792,MONDO:0011160,autosomal recessive nonsyndromic hearing loss 15,
+BMGC_DS12349,BMG_DS041116,,"Deafness, Autosomal Dominant 13",,,,,,,C1866095,C566612,601868,MONDO:0011159,autosomal dominant nonsyndromic hearing loss 13,
+BMGC_DS12350,BMG_DS041117,,"Autoimmune Lymphoproliferative Syndrome, Type IA",,,,,,,C1866119,C566613,,,,
+BMGC_DS12351,BMG_DS041118,,"Autoimmune Lymphoproliferative Syndrome, Type IB",,,,,,,C1866120,C566614,,,,
+BMGC_DS12352,BMG_DS041121,,Vacuolar Neuromyopathy,,,,,,,C1866139,C566617,601846,MONDO:0011155,vacuolar Neuromyopathy,
+BMGC_DS12353,BMG_DS041123,,Phosphoglycerate Dehydrogenase Deficiency,,,,,DOID:0050722,PHGDH deficiency,C1866174,C566618,601815,MONDO:0011152,PHGDH deficiency,
+BMGC_DS12354,BMG_DS041124,,Exudative Vitreoretinopathy 4,,,,,DOID:0111411,exudative vitreoretinopathy 4,C1866176,C566619,601813,MONDO:0011151,exudative vitreoretinopathy 4,
+BMGC_DS12355,BMG_DS041125,,Penttinen-Aula syndrome,,,,,,,C1866182,C536653,601812,MONDO:0011150,acroosteolysis-keloid-like lesions-premature aging syndrome,
+BMGC_DS12356,BMG_DS041126,,"Premature Aging Syndrome, Okamoto Type",,,,,,,C1866183,C566621,601811,MONDO:0011149,"premature aging syndrome, Okamoto type",
+BMGC_DS12357,BMG_DS041127,,Spondylospinal Thoracic Dysostosis,,,,,,,C1866184,C566622,601809,MONDO:0011148,Spondylospinal thoracic dysostosis,
+BMGC_DS12358,BMG_DS041128,,Coloboma-Obesity-Hypogenitalism-Mental Retardation Syndrome,,,,,,,C1866256,C566623,601794,MONDO:0011145,colobomatous microphthalmia - obesity - hypogenitalism - intellectual disability syndrome,
+BMGC_DS12359,BMG_DS041129,,"Peroxisome Biogenesis Disorder, Complementation Group K",,,,,,,C1866257,C566624,,MONDO:0800365,"peroxisome biogenesis disorder, complementation group K",
+BMGC_DS12360,BMG_DS041132,,Retinal cone dystrophy 2,,,,,,,C1866293,C538363,601777,MONDO:0011143,cone-rod dystrophy 6,
+BMGC_DS12361,BMG_DS041133,,,,,,,,,C1866294,,,MONDO:0011142,"Ehlers-Danlos syndrome, musculocontractural type",
+BMGC_DS12362,BMG_DS041134,,Preaxial Hallucal Polydactyly,,,,,,,C1866339,C566632,601759,MONDO:0011139,preaxial hallucal polydactyly,
+BMGC_DS12363,BMG_DS041138,,,,,,,,,C1866373,,601744,MONDO:0011138,"systemic lupus erythematosus, susceptibility to, 1",
+BMGC_DS12364,BMG_DS041139,,Proteus-Like Syndrome,Proteus Syndrome,,,,,,C1866398,D016715,,MONDO:0017571,Proteus-like syndrome,
+BMGC_DS12365,BMG_DS041140,,RETINITIS PIGMENTOSA 19,,,,,,,C1866422,,601691;601718,MONDO:0011137,retinitis pigmentosa 19,
+BMGC_DS12366,BMG_DS041141,,Quebec platelet disorder,,,,,DOID:0111050,Quebec platelet disorder,C1866423,C536260,601709,MONDO:0011136,Quebec platelet disorder,
+BMGC_DS12367,BMG_DS041142,,"Superior Transverse Scapular Ligament, Calcification Of, Familial",,,,,,,C1866424,C566638,601708,MONDO:0011135,"superior transverse scapular ligament, calcification of, familial",
+BMGC_DS12368,BMG_DS041143,,Yemenite deaf-blind hypopigmentation syndrome,,,,,,,C1866425,C536771,601706,MONDO:0011133,"deaf blind hypopigmentation syndrome, Yemenite type",
+BMGC_DS12369,BMG_DS041144,,"T-cell immunodeficiency, congenital alopecia and nail dystrophy",,,,,DOID:0060769,"T-cell immunodeficiency, congenital alopecia, and nail dystrophy",C1866426,C536781,601705,MONDO:0011132,"T-cell immunodeficiency, congenital alopecia, and nail dystrophy",
+BMGC_DS12370,BMG_DS041145,,Arthrogryposis and ectodermal dysplasia,,,,,,,C1866427,C537441,601701,MONDO:0011131,tricho-oculo-dermo-vertebral syndrome,
+BMGC_DS12371,BMG_DS041146,,"Sebaceous gland hyperplasia, familial presenile",,,,,,,C1866428,C537530,601700,MONDO:0011130,"sebaceous gland hyperplasia, familial presenile",
+BMGC_DS12372,BMG_DS041148,,,,,,,,,C1866483,,601682,MONDO:0011129,glaucoma type 1C,
+BMGC_DS12373,BMG_DS041149,,"Bartter syndrome, antenatal type 1",,,,,,,C1866495,C537652,601678,MONDO:0100344,Bartter disease type 1,
+BMGC_DS12374,BMG_DS041151,,Photosensitive Trichothiodystrophy,Trichothiodystrophy Syndromes,,,,DOID:0111868;DOID:2960,photosensitive trichothiodystrophy | nonphotosensitive trichothiodystrophy 5,C1866504,D054463,601675,MONDO:0011125,"trichothiodystrophy 1, photosensitive",
+BMGC_DS12375,BMG_DS041154,,"DIABETES MELLITUS, INSULIN-DEPENDENT, 15",,,,,,,C1866519,,601666,MONDO:0011123,type 1 diabetes mellitus 15,
+BMGC_DS12376,BMG_DS041155,,Paragangliomas 2,,,,,,,C1866552,C566646,601650,MONDO:0011121,paragangliomas 2,
+BMGC_DS12377,BMG_DS041156,,"Neural tube defect, folate-sensitive",,,,,,,C1866558,C536409,601634,MONDO:0011120,"neural tube defects, folate-sensitive",
+BMGC_DS12378,BMG_DS041158,,"Iridogoniodysgenesis, Type 1",,,,,,,C1866560,C535535,601631,MONDO:0024456,anterior segment dysgenesis 3,
+BMGC_DS12379,BMG_DS041160,,Iris Pigment Epithelium Anomalies,,,,,,,C1866608,C566651,601616,MONDO:0011117,iris pigment epithelium anomalies,
+BMGC_DS12380,BMG_DS041161,,Spastic Paraplegia And Evans Syndrome,,,,,,,C1866619,C566652,601608,MONDO:0011115,spastic paraplegia and Evans syndrome,
+BMGC_DS12381,BMG_DS041163,,"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C",,,,,,,C1866636,,608206;601596,MONDO:0011113,Charcot-Marie-Tooth disease type 4C,
+BMGC_DS12382,BMG_DS041164,,Steinfeld Syndrome,,,,,,,C1866649,C566655,184705,MONDO:0008488,holoprosencephaly-radial heart renal anomalies syndrome,
+BMGC_DS12383,BMG_DS041165,,Steatocystoma multiplex with natal teeth,,,,,,,C1866650,C537487,184510,MONDO:0008486,steatocystoma multiplex-natal teeth syndrome,
+BMGC_DS12384,BMG_DS041166,719305006,Stapes ankylosis with broad thumb and toe syndrome,,,,,,,C1866656,,184460,MONDO:0008484,stapes ankylosis with broad thumbs and toes,Stapes ankylosis with broad thumb and toe syndrome (disorder) | Stapes ankylosis with broad thumb and toe syndrome | Teunissen Cremers syndrome
+BMGC_DS12385,BMG_DS041167,,"Spondylometaphyseal dysplasia, Algerian type",,,,,DOID:0112296,spondylometaphyseal dysplasia Algerian type,C1866688,C535794,184253,MONDO:0008478,"spondylometaphyseal dysplasia, Schmidt type",
+BMGC_DS12386,BMG_DS041168,,"Spondyloepiphyseal Dysplasia Tarda, Autosomal Dominant",,,,,,,C1866717,C566658,184100,MONDO:0008474,"spondyloepiphyseal dysplasia tarda, autosomal dominant",
+BMGC_DS12387,BMG_DS041172,,"SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 2",,,,,DOID:0080604,ankylosing spondylitis 2,C1866738,,183840,MONDO:0008468,"spondyloarthropathy, susceptibility to, 2",
+BMGC_DS12388,BMG_DS041174,,"SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS",,,,,,,C1866740,,183800,MONDO:0008466,Karsch-Neugebauer syndrome,
+BMGC_DS12389,BMG_DS041175,,Split-Hand And Split-Foot With Hypodontia,,,,,,,C1866742,C566665,183500,MONDO:0008463,split-hand and split-foot with hypodontia,
+BMGC_DS12390,BMG_DS041176,,,,,,,,,C1866743,,183400,MONDO:0008462,split lower lip,
+BMGC_DS12391,BMG_DS041178,,Splenogonadal fusion limb defects micrognatia,,,,,,,C1866745,C537318,183300,MONDO:0008460,splenogonadal fusion-limb defects-micrognathia syndrome,
+BMGC_DS12392,BMG_DS041179,,Spinocerebellar Atrophy With Pupillary Paralysis,,,,,,,C1866746,C566668,183100,MONDO:0008459,spinocerebellar atrophy with pupillary paralysis,
+BMGC_DS12393,BMG_DS041181,,Spinocerebellar Ataxia With Rigidity And Peripheral Neuropathy,,,,,,,C1866770,C566669,183050,MONDO:0008456,spinocerebellar ataxia with rigidity and peripheral neuropathy,
+BMGC_DS12394,BMG_DS041182,,,,,,,,,C1866774,,183020,MONDO:0008455,"spinal muscular atrophy, segmental",
+BMGC_DS12395,BMG_DS041184,,"Spinal Muscular Atrophy, Facioscapulohumeral Type",,,,,,,C1866783,C566674,182970,MONDO:0008452,"spinal muscular atrophy, facioscapulohumeral type",
+BMGC_DS12396,BMG_DS041185,,"Neuronopathy, Distal Hereditary Motor, Type I",,,,,DOID:0111200,autosomal dominant distal hereditary motor neuronopathy 1,C1866784,C566675,182960,MONDO:0008451,"neuronopathy, distal hereditary motor, autosomal dominant 1",
+BMGC_DS12397,BMG_DS041186,765092004,Spheroid body myopathy,,,,,,,C1866785,C000598645,,,,Spheroid body myopathy | Spheroid body myopathy (disorder)
+BMGC_DS12398,BMG_DS041188,,"Speech Development, Delayed, With Facial Asymmetry, Strabismus, And Transverse Earlobe Crease",,,,,,,C1866802,C566677,182875,MONDO:0008445,delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome,
+BMGC_DS12399,BMG_DS041189,,ELLIPTOCYTOSIS 3,,,,,,,C1866810,,617948;182870,MONDO:0054780,elliptocytosis 3,
+BMGC_DS12400,BMG_DS041190,,"Spastic Paraplegia, Optic Atrophy, And Dementia",,,,,,,C1866849,C566679,182830,MONDO:0008444,"spastic paraplegia, optic atrophy, and dementia",
+BMGC_DS12401,BMG_DS041192,,Spastic paraplegia neuropathy poikiloderma,,,,,,,C1866851,C536870,182815,MONDO:0008442,spastic paraplegia-neuropathy-poikiloderma syndrome,
+BMGC_DS12402,BMG_DS041193,,Spastic Paraplegia With Associated Extrapyramidal Signs,,,,,,,C1866852,C566681,182800,MONDO:0008441,spastic paraplegia with associated extrapyramidal signs,
+BMGC_DS12403,BMG_DS041194,,"Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, And Progressive Nephropathy",,,,,,,C1866853,C566682,182690,MONDO:0008440,spastic paraplegia-nephritis-deafness syndrome,
+BMGC_DS12404,BMG_DS041196,,"Spastic paraplegia 4, autosomal dominant",,,,,,,C1866855,C536865,182601,MONDO:0008438,hereditary spastic paraplegia 4,
+BMGC_DS12405,BMG_DS041198,,Skeletal Dysplasia With Delayed Epiphyseal And Carpal Bone Ossification,,,,,,,C1866939,C566687,182255,MONDO:0008430,skeletal dysplasia with delayed epiphyseal and carpal bone ossification,
+BMGC_DS12406,BMG_DS041200,,Shprintzen omphalocele syndrome,,,,,,,C1866958,C537329,182210,MONDO:0008425,"omphalocele syndrome, Shprintzen-Goldberg type",
+BMGC_DS12407,BMG_DS041201,,,,,,,,,C1866959,,182200,MONDO:0008424,"sella turcica, bridged",
+BMGC_DS12408,BMG_DS041202,,Sinus Node Disease and Myopia,,,,,,,C1866960,C566690,182190,MONDO:0008423,sinus node disease and myopia,
+BMGC_DS12409,BMG_DS041203,,Simosa cranio facial syndrome,,,,,,,C1866962,C537339,182150,MONDO:0008421,flat face-microstomia-ear anomaly syndrome,
+BMGC_DS12410,BMG_DS041204,,"SCLERODERMA, FAMILIAL PROGRESSIVE",,,,,,,C1866983,,181750,MONDO:0008418,"scleroderma, familial progressive",
+BMGC_DS12411,BMG_DS041206,722002002,Scholte syndrome,,,,,,,C1866985,C536638,300977,MONDO:0010505,intellectual disability-balding-patella luxation-acromicria syndrome,"Intellectual disability, balding, patella luxation, acromicria syndrome (disorder) | Intellectual disability, balding, patella luxation, acromicria syndrome | Scholte Begeer-van Essen syndrome | Scholte syndrome"
+BMGC_DS12412,BMG_DS041208,700211007,Ulnar-mammary syndrome,,,,,DOID:0060614,ulnar-mammary syndrome,C1866994,C536937,181450,MONDO:0008411,ulnar-mammary syndrome,Ulnar mammary syndrome | Ulnar mammary syndrome (disorder) | Ulnar-mammary syndrome | Schinzel syndrome
+BMGC_DS12413,BMG_DS041209,,"Scapuloperoneal Syndrome, Neurogenic, Kaeser Type",,,,,DOID:0111551,neurogenic scapuloperoneal syndrome Kaeser type,C1867005,C566695,181400,MONDO:0008407,"neurogenic scapuloperoneal syndrome, Kaeser type",
+BMGC_DS12414,BMG_DS041210,,SCALP-EAR-NIPPLE SYNDROME,,,,,DOID:0111550,scalp-ear-nipple syndrome,C1867020,,181270;613420,MONDO:0008404,scalp-ear-nipple syndrome,
+BMGC_DS12415,BMG_DS041211,,Scalp defects postaxial polydactyly,,,,,,,C1867021,C536622,181250,MONDO:0008403,scalp defects-postaxial polydactyly syndrome,
+BMGC_DS12416,BMG_DS041212,,Say syndrome,,,,,,,C1867023,C536621,181180,MONDO:0008402,cleft palate-large ears-small head syndrome,
+BMGC_DS12417,BMG_DS041218,,Robinow Sorauf syndrome,,,,,,,C1867146,C537183,180750,MONDO:0008391,Robinow-Sorauf syndrome,
+BMGC_DS12418,BMG_DS041219,721904001,Rombo syndrome,,,,,,,C1867147,C535870,180730,MONDO:0008390,Rombo syndrome,Rombo syndrome (disorder) | Rombo syndrome
+BMGC_DS12419,BMG_DS041220,,RING DERMOID OF CORNEA,,,,,DOID:0111548,ring dermoid of cornea,C1867155,,601542;180550,MONDO:0008387,ring dermoid of cornea,
+BMGC_DS12420,BMG_DS041221,,,,,,,,,C1867222,,180360,MONDO:0008385,rhiny,
+BMGC_DS12421,BMG_DS041222,,,,,,,,,C1867234,,180295,MONDO:0859046,"rhabdomyosarcoma, embryonal, 2",
+BMGC_DS12422,BMG_DS041225,,"Retinopathy, Pericentral Pigmentary, Dominant",,,,,,,C1867261,C566713,180210,MONDO:0008381,dominant pericentral pigmentary retinopathy,
+BMGC_DS12423,BMG_DS041226,,Retinitis Pigmentosa 10,,,,,DOID:0110388,retinitis pigmentosa 10,C1867299,C566715,180105,MONDO:0008379,retinitis pigmentosa 10,
+BMGC_DS12424,BMG_DS041227,,RETINITIS PIGMENTOSA 9,,,,,,,C1867300,,180104;607331,MONDO:0008378,retinitis pigmentosa 9,
+BMGC_DS12425,BMG_DS041229,,RETINAL CONE DYSTROPHY 1,,,,,,,C1867326,,180020,MONDO:0008374,retinal cone dystrophy type 1,
+BMGC_DS12426,BMG_DS041231,,Reticular Dystrophy Of Retinal Pigment Epithelium,,,,,,,C1867332,C566721,179840,MONDO:0009979,reticular dystrophy of the retinal pigment epithelium,
+BMGC_DS12427,BMG_DS041232,,Red cell phospholipid defect with hemolysis,,,,,,,C1867339,C535298,179700,MONDO:0008367,red cell phospholipid defect with hemolysis,
+BMGC_DS12428,BMG_DS041234,,,,,,,,,C1867393,,179500,MONDO:0008363,raindrop hypopigmentation,
+BMGC_DS12429,BMG_DS041236,,"RADIUS, APLASIA OF, WITH CLEFT LIP/PALATE",,,,,,,C1867395,,179400,MONDO:0008361,"radius, aplasia of, with cleft lip/palate",
+BMGC_DS12430,BMG_DS041237,,RADIAL-RENAL SYNDROME,,,,,,,C1867396,,179280,,,
+BMGC_DS12431,BMG_DS041238,,"Radial hypoplasia, triphalangeal thumbs and hypospadias",,,,,,,C1867397,C536262,179250,MONDO:0008357,radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome,
+BMGC_DS12432,BMG_DS041239,,"Radial Heads, Posterior Dislocation Of",,,,,,,C1867398,C566728,179200,MONDO:0008356,"radial heads, posterior dislocation of",
+BMGC_DS12433,BMG_DS041240,,Infantile Hypertrophic Pyloric Stenosis,"Pyloric Stenosis, Hypertrophic",,,,,,C1867403,D046248,179010,MONDO:0001560;MONDO:0008355,"hypertrophic pyloric stenosis | pyloric stenosis, infantile hypertrophic, 1",
+BMGC_DS12434,BMG_DS041241,,PULMONIC STENOSIS AND DEAFNESS,,,,,,,C1867406,,178651,MONDO:0008350,pulmonic stenosis and deafness,
+BMGC_DS12435,BMG_DS041242,,Ciuffo Syndrome,,,,,,,C1867407,C566733,178650,MONDO:0008349,"pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities",
+BMGC_DS12436,BMG_DS041244,,Pubic Bone Dysplasia,,,,,,,C1867436,C566735,178350,MONDO:0008342,pubic bone dysplasia,
+BMGC_DS12437,BMG_DS041245,,"Ptosis, Strabismus, And Ectopic Pupils",,,,,,,C1867437,C566736,178330,MONDO:0008341,ptosis-strabismus-ectopic pupils syndrome,
+BMGC_DS12438,BMG_DS041246,,"Ptosis, Hereditary Congenital 1",,,,,,,C1867438,C566737,178300,MONDO:0008340,"ptosis, hereditary congenital, 1",
+BMGC_DS12439,BMG_DS041247,,"Pterygium, Antecubital",,,,,,,C1867439,C566738,178200,MONDO:0008339,antecubital pterygium syndrome,
+BMGC_DS12440,BMG_DS041248,771269000,Autosomal dominant multiple pterygium syndrome,,,,,,,C1867440,,178110,MONDO:0008338,"contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A",Autosomal dominant multiple pterygium syndrome (disorder) | Distal arthrogryposis type 8 | Autosomal dominant multiple pterygium syndrome
+BMGC_DS12441,BMG_DS041249,,"Pterygium Colli, Isolated",,,,,,,C1867442,C566741,177990,MONDO:0008336,"pterygium colli, isolated",
+BMGC_DS12442,BMG_DS041250,716090004,Haspeslagh Fryns Muelenaere syndrome,,,,,,,C1867443,C535844,177980,MONDO:0008335,short stature-craniofacial anomalies-genital hypoplasia syndrome,Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Short stature with craniofacial anomalies and genital hypoplasia syndrome | Haspeslagh Fryns Muelenaere syndrome
+BMGC_DS12443,BMG_DS041251,,,,,,,,,C1867449,,177900,MONDO:0008334,"psoriasis 1, susceptibility to",
+BMGC_DS12444,BMG_DS041252,,"Pseudoxanthoma Elasticum, Incomplete",Pseudoxanthoma Elasticum,,,,,,C1867450,D011561,177850,MONDO:0008333,"pseudoxanthoma elasticum, forme fruste",
+BMGC_DS12445,BMG_DS041256,,"Butyrylcholinesterase Deficiency, Fluoride-Resistant, Japanese Type",,,,,,,C1867469,C566751,,,,
+BMGC_DS12446,BMG_DS041259,,"Pruritus, Hereditary Localized",,,,,,,C1867499,C566754,177100,MONDO:0008321,"pruritus, hereditary localized",
+BMGC_DS12447,BMG_DS041262,,,,,,,,,C1867616,,,MONDO:0021454,benign neoplasm of eye,
+BMGC_DS12448,BMG_DS041265,1293192009,Premature coronary artery disease,,,,,,,C1867743,,,,,Premature coronary artery disease | Premature coronary artery disease (disorder) | PCAD - premature coronary artery disease
+BMGC_DS12449,BMG_DS041266,,Primary Release Disorder Of Platelets,,,,,,,C1867770,C566759,176630,MONDO:0008309,primary release disorder of platelets,
+BMGC_DS12450,BMG_DS041268,,"Presenile dementia, Kraepelin type",,,,,,,C1867772,C535273,176600,MONDO:0008307,"presenile dementia, Kraepelin type",
+BMGC_DS12451,BMG_DS041271,,"Preaxial deficiency, postaxial polydactyly and hypospadias",,,,,DOID:0111544,Guttmacher syndrome,C1867801,C538278,176305,MONDO:0008301,Guttmacher syndrome,
+BMGC_DS12452,BMG_DS041273,,LONG QT SYNDROME 5,,,,,,,C1867904,,176261;613695,MONDO:0013372,long QT syndrome 5,
+BMGC_DS12453,BMG_DS041274,,Posterior column ataxia,,,,,,,C1867923,C536342,176250,MONDO:0008299,posterior column ataxia,
+BMGC_DS12454,BMG_DS041275,,,,,,,,,C1867924,,176240,MONDO:0008298,postaxial tetramelic oligodactyly,
+BMGC_DS12455,BMG_DS041276,,"Porphyria Cutanea Tarda, Type I",,,,,,,C1867968,C566768,176090,MONDO:0008295,sporadic porphyria cutanea tarda,
+BMGC_DS12456,BMG_DS041277,,"Porphyria, Acute Intermittent, Nonerythroid Variant",,,,,,,C1867969,C566769,,,,
+BMGC_DS12457,BMG_DS041278,,"POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC, 1",,,,,,,C1867981,,175900,MONDO:0008293,"porokeratosis 3, disseminated superficial actinic type",
+BMGC_DS12458,BMG_DS041279,,,,,,,,,C1867982,,175860,MONDO:0008292,punctate palmoplantar keratoderma type 2,
+BMGC_DS12459,BMG_DS041280,1162864000,Familial porencephaly,,,,,DOID:0060263,porencephaly,C1867983,,,MONDO:0020496,familial porencephaly,Familial porencephaly (disorder) | Familial porencephalic cyst | Familial porencephaly
+BMGC_DS12460,BMG_DS041283,,,,,,,,,C1868001,,175505,MONDO:0008284,polyposis of gastric fundus without polyposis coli,
+BMGC_DS12461,BMG_DS041284,,,,,,,,,C1868005,,175450,MONDO:0008282,"polyposis, intestinal, with multiple exostoses",
+BMGC_DS12462,BMG_DS041285,,,,,,,,,C1868006,,175400,MONDO:0008281,"polyposis, intestinal, scattered and discrete",
+BMGC_DS12463,BMG_DS041288,,Juvenile Polyposis Coli,,,,,DOID:0050787,juvenile polyposis syndrome,C1868081,C537702,,MONDO:0008276,generalized juvenile polyposis/juvenile polyposis coli,
+BMGC_DS12464,BMG_DS041290,,,,,,,,,C1868111,,174700,MONDO:0008272,polysyndactyly 4,
+BMGC_DS12465,BMG_DS041292,,"Polydactyly, Preaxial III",,,,,,,C1868113,C566784,174600,MONDO:0008271,polydactyly of an index finger,
+BMGC_DS12466,BMG_DS041293,,,,,,,,,C1868114,,174500,MONDO:0008270,polydactyly of a triphalangeal thumb,
+BMGC_DS12467,BMG_DS041294,,"POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA",,,,,,,C1868117,,174310,MONDO:0008268,polydactyly-myopia syndrome,
+BMGC_DS12468,BMG_DS041295,,Orofaciodigital syndrome 5,,,,,DOID:0060375,orofaciodigital syndrome V,C1868118,C557819,174300,MONDO:0008267,orofaciodigital syndrome V,
+BMGC_DS12469,BMG_DS041296,,,,,,,,,C1868120,,,MONDO:0019674,postaxial polydactyly type B,
+BMGC_DS12470,BMG_DS041297,726017001,Medullary cystic kidney disease 1,,,,,,,C1868139,C536137,174000,MONDO:0020726,"tubulointerstitial kidney disease, autosomal dominant, 2",Autosomal dominant medullary cystic kidney disease without hyperuricemia | Autosomal dominant medullary cystic kidney disease without hyperuricaemia | Medullary cystic kidney disease 1 | Mucin 1 related autosomal dominant tubulointerstitial kidney disease (disorder) | MUC1-related autosomal dominant tubulointerstitial kidney disease | Mucin 1 related autosomal dominant tubulointerstitial kidney disease
+BMGC_DS12471,BMG_DS041300,,"PNEUMOTHORAX, PRIMARY SPONTANEOUS",,,,,DOID:0080218,primary spontaneous pneumothorax,C1868193,,607273;173600,MONDO:0008259,familial spontaneous pneumothorax,
+BMGC_DS12472,BMG_DS041301,,Platelet Signal Processing Defect,,,,,,,C1868199,C566796,173590,MONDO:0008258,platelet signal processing defect,
+BMGC_DS12473,BMG_DS041305,,Platelet Factor 3 Deficiency,,,,,,,C1868256,C566798,173450,MONDO:0008255,platelet factor 3 deficiency,
+BMGC_DS12474,BMG_DS041306,,"Platelet Disorder, Undefined",,,,,,,C1868258,C566799,173420,MONDO:0008254,"platelet disorder, undefined",
+BMGC_DS12475,BMG_DS041309,,Robin sequence and oligodactyly,,,,,,,C1868309,C535688,172880,MONDO:0008247,Robin sequence-oligodactyly syndrome,
+BMGC_DS12476,BMG_DS041310,,Pigmented Paravenous Chorioretinal Atrophy,,,,,DOID:0111541,pigmented paravenous chorioretinal atrophy,C1868310,C566801,172870,MONDO:0008246,pigmented paravenous retinochoroidal atrophy,
+BMGC_DS12477,BMG_DS041311,773984007,Telfer Sugar Jaeger syndrome,,,,,,,C1868311,C536955,172850,MONDO:0008245,piebald trait-neurologic defects syndrome,Piebald trait with neurologic defects syndrome | Piebald trait with neurologic defects syndrome (disorder) | Telfer Sugar Jaeger syndrome
+BMGC_DS12478,BMG_DS041313,,6-Phosphogluconolactonase Deficiency,,,,,,,C1868355,C566803,172150,MONDO:0008240,6-phosphogluconolactonase deficiency,
+BMGC_DS12479,BMG_DS041316,,Phlebectasia Of Lips,,,,,,,C1868391,C566806,171450,MONDO:0008236,phlebectasia of lips,
+BMGC_DS12480,BMG_DS041317,,,,,,,,,C1868392,,171420,MONDO:0008235,pheochromocytoma-islet cell tumor syndrome,
+BMGC_DS12481,BMG_DS041320,,Accessory deep peroneal nerve,,,,,,,C1868426,C536001,170980,MONDO:0008229,"peroneal nerve, accessory deep",
+BMGC_DS12482,BMG_DS041321,,"Normokalemic Periodic Paralysis, Potassium-Sensitive",,,,,,,C1868433,C566809,,,,
+BMGC_DS12483,BMG_DS041325,,Pelvis-Shoulder Dysplasia,,,,,,,C1868508,C566811,169550,MONDO:0008217,pelvis-shoulder dysplasia,
+BMGC_DS12484,BMG_DS041326,,Pelvic Lipomatosis with Crossed Renal Ectopia,,,,,,,C1868511,C566812,169545,MONDO:0008216,pelvic lipomatosis with crossed renal ectopia,
+BMGC_DS12485,BMG_DS041327,,"Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant",,,,,,,C1868512,C566813,169500,MONDO:0008215,adult-onset autosomal dominant demyelinating leukodystrophy,
+BMGC_DS12486,BMG_DS041328,,Pechet Factor Deficiency,,,,,,,C1868545,C566814,169200,MONDO:0008212,Pechet factor deficiency,
+BMGC_DS12487,BMG_DS041330,,Patterned dystrophy of retinal pigment epithelium,,,,,,,C1868569,C536309,,MONDO:0018973,patterned dystrophy of the retinal pigment epithelium,
+BMGC_DS12488,BMG_DS041331,,CHAR SYNDROME,,,,,,,C1868570,,601601;169100,MONDO:0008209,Char syndrome,
+BMGC_DS12489,BMG_DS041333,,"Paroxysmal Tonic Upgaze, Benign Childhood, With Ataxia",,,,,,,C1868576,C566817,168885,MONDO:0008206,benign paroxysmal tonic upgaze of childhood with ataxia,
+BMGC_DS12490,BMG_DS041334,,,,,,,,,C1868577,,168860,MONDO:0008205,patella aplasia/hypoplasia,
+BMGC_DS12491,BMG_DS041335,,"Patella aplasia, coxa vara, tarsal synostosis",,,,,DOID:0111382,ischiocoxopodopatellar syndrome,C1868581,C536307,168850,MONDO:0008204," | obsolete patella aplasia, coxa vara, and tarsal synostosis",
+BMGC_DS12492,BMG_DS041336,,"Parotidomegaly, Hereditary Bilateral",,,,,,,C1868590,C566821,168800,MONDO:0008202,"Parotidomegaly, hereditary bilateral",
+BMGC_DS12493,BMG_DS041337,,Perry Syndrome,,,,,DOID:0060486,Perry syndrome,C1868594,C566822,168605,MONDO:0008201,Perry syndrome,
+BMGC_DS12494,BMG_DS041338,,"PARKINSON DISEASE 1, AUTOSOMAL DOMINANT",,,,,DOID:0060367,Parkinson's disease 1,C1868595,,163890;168601,MONDO:0008200,autosomal dominant Parkinson disease 1,
+BMGC_DS12495,BMG_DS041340,,Parietal Foramina With Cleidocranial Dysplasia,,,,,,,C1868597,C566825,168550,MONDO:0008198,parietal foramina with cleidocranial dysplasia,
+BMGC_DS12496,BMG_DS041341,,,,,,,DOID:0060285,parietal foramina,C1868598,,,,,
+BMGC_DS12497,BMG_DS041342,,,,,,,,,C1868599,,168500,MONDO:0008197,parietal foramina 1,
+BMGC_DS12498,BMG_DS041343,,,,,,,DOID:0111539,parastremmatic dwarfism,C1868616,,168400,MONDO:0008196,parastremmatic dwarfism,
+BMGC_DS12499,BMG_DS041344,,Paramyotonia Congenita Without Cold Paralysis,Myotonic Disorders,,,,,,C1868619,D020967,,,,
+BMGC_DS12500,BMG_DS041345,,Paragangliomas with Sensorineural Hearing Loss,,,,,,,C1868633,C566831,,,,
+BMGC_DS12501,BMG_DS041346,,,,,,,,,C1868647,,167950,MONDO:0008189,"papillomatosis, florid, of nipple",
+BMGC_DS12502,BMG_DS041347,,,,,,,,,C1868649,,167870,MONDO:0008187,panic disorder 1,
+BMGC_DS12503,BMG_DS041353,723411003,Nasopalpebral lipoma coloboma syndrome,,,,,,,C1868660,C538338,167730,MONDO:0008182,nasopalpebral lipoma-coloboma syndrome,Nasopalpebral lipoma coloboma syndrome (disorder) | Nasopalpebral lipoma coloboma syndrome
+BMGC_DS12504,BMG_DS041354,,,,,,,,,C1868661,,167600,MONDO:0008181,"palmaris longus muscle, absence of",
+BMGC_DS12505,BMG_DS041355,,"NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE",,,,,DOID:0080379,nephrotic syndrome type 2,C1868672,,600995,MONDO:0010974,"nephrotic syndrome, type 2",
+BMGC_DS12506,BMG_DS041356,,"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE",,,,,DOID:0060368,Parkinson's disease 2,C1868675,,600116;602544,MONDO:0010820,autosomal recessive juvenile Parkinson disease 2,
+BMGC_DS12507,BMG_DS041357,,PHOTOPAROXYSMAL RESPONSE 1,,,,,,,C1868677,,132100,MONDO:0007559,photoparoxysmal response 1,
+BMGC_DS12508,BMG_DS041358,,"Thanatophoric Dysplasia, Type I",,,,,,,C1868678,C566844,187600;270230,MONDO:0008546,thanatophoric dysplasia type 1,
+BMGC_DS12509,BMG_DS041359,,"GRISCELLI SYNDROME, TYPE 2",,,,,DOID:0060833,Griscelli syndrome type 2,C1868679,,603868;607624,MONDO:0011872,Griscelli syndrome type 2,
+BMGC_DS12510,BMG_DS041360,,DYSTONIA 12,,,,,,,C1868681,,128235;182350,MONDO:0007496,dystonia 12,
+BMGC_DS12511,BMG_DS041361,49949003;609221008;51938001,Paroxysmal kinesigenic choreoathetosis,,,,,,,C1868682,C537180,MTHU070263,MONDO:0044202,episodic kinesigenic dyskinesia,Paroxysmal choreoathetosis | Paroxysmal choreoathetosis (disorder) | Paroxysmal dyskinesia | Paroxysmal kinesigenic dyskinesia (disorder) | Paroxysmal kinesigenic choreoathetosis | Paroxysmal kinesigenic dyskinesia | Paroxysmal kinesigenic choreoathetosis | Paroxysmal kinesigenic choreoathetosis (disorder)
+BMGC_DS12512,BMG_DS041362,,,,,,,,,C1868683,,109543,MONDO:0007190,"leukemia, chronic lymphocytic, susceptibility to, 2",
+BMGC_DS12513,BMG_DS041363,,"EAR, PATELLA, SHORT STATURE SYNDROME",,,,,DOID:0060306;DOID:0080512,Meier-Gorlin syndrome 1 | Meier-Gorlin syndrome,C1868684,,224690,MONDO:0016817,Meier-Gorlin syndrome,
+BMGC_DS12514,BMG_DS041364,,,,,,,,,C1868685,,,MONDO:0007462,"multiple sclerosis, susceptibility to",
+BMGC_DS12515,BMG_DS041365,41371000119100,Shone complex,,,,,,,C1868705,,,MONDO:0020404,shone complex,Shone complex | Shone syndrome | Shone complex (disorder)
+BMGC_DS12516,BMG_DS041368,,Periventricular Nodular Heterotopia,Periventricular Nodular Heterotopia,,,,DOID:0050454,periventricular nodular heterotopia,C1868720,D054091,,MONDO:0020341,periventricular nodular heterotopia,
+BMGC_DS12517,BMG_DS041371,,diabetic encephalopathy,,,,,,,C1868773,C000721848,,MONDO:0000489,diabetic encephalopathy,
+BMGC_DS12518,BMG_DS041374,,,,,,,,,C1868854,,,MONDO:0017285,penoscrotal transposition,
+BMGC_DS12519,BMG_DS041375,440630006,Irritable bowel syndrome characterized by constipation,,,,,,,C1868889,,,,,Irritable bowel syndrome characterized by constipation (disorder) | Constipation predominant irritable bowel syndrome | Irritable bowel syndrome characterised by constipation | Irritable bowel syndrome characterized by constipation
+BMGC_DS12520,BMG_DS041378,,"Weill-Marchesani Syndrome, Autosomal Recessive",Weill-Marchesani Syndrome,,,,DOID:0050475,Weill-Marchesani syndrome,C1869114,D056846,,,,
+BMGC_DS12521,BMG_DS041379,,"Weill-Marchesani Syndrome, Autosomal Dominant",Weill-Marchesani Syndrome,,,,DOID:0050475,Weill-Marchesani syndrome,C1869115,D056846,608328,MONDO:0012013,"Weill-Marchesani syndrome 2, dominant",
+BMGC_DS12522,BMG_DS041380,,,,,,,,,C1869116,,600807,MONDO:0010940,inherited susceptibility to asthma,
+BMGC_DS12523,BMG_DS041381,609218006,Paroxysmal nonkinesigenic dyskinesia,,,,,,,C1869117,,MTHU000808,MONDO:0700088,paroxysmal nonkinesigenic dyskinesia,Mount-Reback syndrome | Paroxysmal dystonic choreoathetosis | Paroxysmal nonkinesigenic dyskinesia (disorder) | Paroxysmal nonkinesigenic dyskinesia | Familial paroxysmal choreoathetosis
+BMGC_DS12524,BMG_DS041382,,,,,,,,,C1869118,,218700,MONDO:0024264,"hypothyroidism, congenital, nongoitrous, 2",
+BMGC_DS12525,BMG_DS041383,,,,,,,DOID:0050802,Ehlers-Danlos syndrome spondylodysplastic type 2,C1869122,,,,,
+BMGC_DS12526,BMG_DS041384,,Limb-girdle muscular dystrophy type 2A,,,,,,,C1869123,C535895,253600,MONDO:0009675,autosomal recessive limb-girdle muscular dystrophy type 2A,
+BMGC_DS12527,BMG_DS041385,,"CEROID LIPOFUSCINOSIS, NEURONAL, 2",,,,,,,C1876161,,204500;607998,MONDO:0008769,neuronal ceroid lipofuscinosis 2,
+BMGC_DS12528,BMG_DS041387,,Copper-Overload Cirrhosis,,,,,,,C1876165,C566858,,,,
+BMGC_DS12529,BMG_DS041392,,,,,,,,,C1876174,,,MONDO:0800415,"asthma, aspirin-induced, susceptibility to",
+BMGC_DS12530,BMG_DS041393,,Ataxia-Telangiectasia Variant,,,,,,,C1876175,C566865,,MONDO:0018266,ataxia - telangiectasia variant,
+BMGC_DS12531,BMG_DS041395,,,,,,,,,C1876177,,102300,MONDO:0007053,"restless legs syndrome, susceptibility to, 1",
+BMGC_DS12532,BMG_DS041396,,,,,,,,,C1876179,,108000,MONDO:0007153,"arteries, anomalies of",
+BMGC_DS12533,BMG_DS041397,,"EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS",,,,,,,C1876181,,133705,MONDO:0007587,external auditory canal atresia-vertical talus-hypertelorism syndrome,
+BMGC_DS12534,BMG_DS041398,,"NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2",,,,,DOID:0110863,congenital stationary night blindness autosomal dominant 2,C1876182,,163500;180072,MONDO:0008099,congenital stationary night blindness autosomal dominant 2,
+BMGC_DS12535,BMG_DS041399,,,,,,,,,C1876184,,186400,MONDO:0008518,calcaneonavicular coalition,
+BMGC_DS12536,BMG_DS041400,,Dysgnathia complex,,,,,,,C1876185,C537996,,,,
+BMGC_DS12537,BMG_DS041401,,"TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL",,,,,,,C1876187,,211900,MONDO:0100251,familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome,
+BMGC_DS12538,BMG_DS041402,,,,,,,,,C1876203,,,MONDO:0016643,frontonasal dysplasia,
+BMGC_DS12539,BMG_DS041404,,Hereditary bundle branch system defect,,,,,,,C1879286,C566873,113900,MONDO:0007240,"progressive familial heart block, type 1A",
+BMGC_DS12540,BMG_DS041405,,,,,,,DOID:0081087,acute myeloid leukemia with maturation,C1879321,,,MONDO:0020320,acute myeloblastic leukemia with maturation,
+BMGC_DS12541,BMG_DS041408,190694001;56595005,Hypertyrosinemia,,,,E70.21,,,C1879362,,,,,Tyrosinemia | Tyrosinaemia | Tyrosinemia (disorder) | Hypertyrosinemia | Elevated tyrosine blood level | Hypertyrosinaemia | Hypertyrosinemia (disorder)
+BMGC_DS12542,BMG_DS041414,425582007,Inappropriate sinus tachycardia,,,,,,,C1881170,,,,,Inappropriate sinus tachycardia (disorder) | Inappropriate sinus tachycardia
+BMGC_DS12543,BMG_DS041421,,,,,,,,,C1883486,,,MONDO:0006003,uterine corpus cancer,
+BMGC_DS12544,BMG_DS041431,,Human Herpesvirus 6 encephalitis,,,,,,,C1955629,C538117,,MONDO:0027029,HHV-6 encephalitis,
+BMGC_DS12545,BMG_DS041434,,Glucocorticoid deficiency,,,,,,,C1955741,,MTHU059312,,,
+BMGC_DS12546,BMG_DS041445,,,,,,,,,C1955861,,,MONDO:0019469,T-cell large granular lymphocyte leukemia,
+BMGC_DS12547,BMG_DS041446,,Malformations of Cortical Development,Malformations of Cortical Development,,,,,,C1955869,D054220,,,,
+BMGC_DS12548,BMG_DS041447,,Classical Lissencephalies and Subcortical Band Heterotopias,Classical Lissencephalies and Subcortical Band Heterotopias,,,,DOID:0060402,chromosome 17p13.1 deletion syndrome,C1955870,D054221,,,,
+BMGC_DS12549,BMG_DS041449,,Trichothiodystrophy Syndromes,Trichothiodystrophy Syndromes,,,,DOID:0111868;DOID:0111866;DOID:2960,trichothiodystrophy | photosensitive trichothiodystrophy | nonphotosensitive trichothiodystrophy 5,C1955934,D054463,,MONDO:0018053,trichothiodystrophy,
+BMGC_DS12550,BMG_DS041451,,Paris-Trousseau Thrombocytopenia,Jacobsen Distal 11q Deletion Syndrome,,,,DOID:0111723,Jacobsen Syndrome,C1956093,D054868,188025,MONDO:0008557,Paris-Trousseau thrombocytopenia,
+BMGC_DS12551,BMG_DS041452,,Wolf-Hirschhorn Syndrome,Wolf-Hirschhorn Syndrome,,,,DOID:0050460,Wolf-Hirschhorn syndrome,C1956097,D054877,194190,MONDO:0008684,Wolf-Hirschhorn syndrome,
+BMGC_DS12552,BMG_DS041453,,Alagille Syndrome 1,Alagille Syndrome,,,,,,C1956125,D016738,118450,MONDO:0016862,Alagille syndrome due to a JAG1 point mutation,
+BMGC_DS12553,BMG_DS041454,,,,,,,,,C1956147,,,MONDO:0015204,microlissencephaly,
+BMGC_DS12554,BMG_DS041456,,"Hematoma, Basal Ganglia",Basal Ganglia Hemorrhage,,,,,,C1956233,D020145,,,,
+BMGC_DS12555,BMG_DS041459,,Pulmonary Stenosis,Pulmonary Valve Stenosis,,,,,,C1956257,D011666,265500,MONDO:0020395;MONDO:0009938,pulmonic stenosis | valvar pulmonary stenosis,
+BMGC_DS12556,BMG_DS041460,,Familial Thrombotic Thrombocytopenic Purpura,"Purpura, Thrombotic Thrombocytopenic",,,,,,C1956258,D011697,,,,
+BMGC_DS12557,BMG_DS041461,,Coronary Artery Disease,Coronary Artery Disease,,,,,,C1956346,D003324,,MONDO:0005010,coronary artery disorder,
+BMGC_DS12558,BMG_DS041462,,"Cerebral Amyloid Angiopathy, Genetic","Cerebral Amyloid Angiopathy, Familial",,,,DOID:9246,cerebral amyloid angiopathy,C1956349,D028243,,,,
+BMGC_DS12559,BMG_DS041464,,Cranial Arteritis,Giant Cell Arteritis,,,,,,C1956390,D013700,,,,
+BMGC_DS12560,BMG_DS041465,,Temporal Arteritis,Giant Cell Arteritis,,,,,,C1956391,D013700,187360,MONDO:0008538,temporal arteritis,
+BMGC_DS12561,BMG_DS041469,,"Double Outlet Right Ventricle, Subaortic VSD",Double Outlet Right Ventricle,,,,,,C1956411,D004310,,,,
+BMGC_DS12562,BMG_DS041473,,PTEN Hamartoma Tumor Syndrome,"Hamartoma Syndrome, Multiple",,,,DOID:0050657,Bannayan-Riley-Ruvalcaba syndrome,C1959582,D006223,,MONDO:0017623,PTEN hamartoma tumor syndrome,
+BMGC_DS12563,BMG_DS041474,,Myocardial Failure,Heart Failure,,,,,,C1959583,D006333,,,,
+BMGC_DS12564,BMG_DS041478,,Dihydropyrimidine Dehydrogenase Deficiency,Dihydropyrimidine Dehydrogenase Deficiency,,,,DOID:14218,dihydropyrimidine dehydrogenase deficiency,C1959620,D054067,274270,MONDO:0010130,dihydropyrimidine dehydrogenase deficiency,
+BMGC_DS12565,BMG_DS041479,,Mevalonic Aciduria,Mevalonate Kinase Deficiency,,,,DOID:0050452,mevalonic aciduria,C1959626,D054078,610377,MONDO:0012481,mevalonic aciduria,
+BMGC_DS12566,BMG_DS041484,427649000,Calcium renal calculus,,,,,,,C1959799,,,,,Calcium renal calculus (disorder) | Calcium renal calculus
+BMGC_DS12567,BMG_DS041499,427617000,Aphthous ulceration of skin and/or mucous membrane (disorder),,,,,,,C1959869,,,,,Aphthous ulceration of skin and/or mucous membrane (disorder) | Aphthous ulceration of skin and/or mucous membrane | Aphthous ulceration | Aphthosis | Aphthous ulcer
+BMGC_DS12568,BMG_DS041545,,,,,,,,,C1960398,,,MONDO:0006244,HER2 positive breast carcinoma,
+BMGC_DS12569,BMG_DS041558,427167008,Hereditary angioedema with normal C1 esterase inhibitor activity,,,,,,,C1960459,,,MONDO:0100567,hereditary angioedema with normal C1Inh,Hereditary angioneurotic oedema with normal C1 esterase inhibitor activity | Hereditary angioedema - type 3 | Hereditary angio-oedema with normal C1 esterase inhibitor activity | Hereditary angioedema with normal C1 esterase inhibitor activity | Hereditary angioneurotic edema with normal C1 esterase inhibitor activity | Hereditary angioedema with normal C1 esterase inhibitor activity (disorder)
+BMGC_DS12570,BMG_DS041561,427608000,Left ventricular noncompaction,,,,,,,C1960469,,MTHU038630,MONDO:0018901,left ventricular noncompaction,Left ventricular noncompaction (disorder) | Left ventricular noncompaction
+BMGC_DS12571,BMG_DS041572,,Aromatase deficiency,,,,,,,C1960539,C537436,613546,MONDO:0013301,aromatase deficiency,
+BMGC_DS12572,BMG_DS041593,426387005,Long-chain fatty acid transport deficiency,,,,,,,C1960675,,,,,Long-chain fatty acid transport deficiency (disorder) | Long-chain fatty acid transport deficiency
+BMGC_DS12573,BMG_DS041602,426549001,Crohn's disease in remission,,,,,,,C1960764,,,,,Crohn's disease in remission (disorder) | Crohn's disease in remission | Crohn disease in remission
+BMGC_DS12574,BMG_DS041621,426087004,Right-sided Staphylococcus aureus endocarditis,,,,,,,C1960924,,,,,Right-sided Staphylococcus aureus endocarditis (disorder) | Right-sided Staphylococcus aureus endocarditis
+BMGC_DS12575,BMG_DS041630,,,,,,,,,C1961099,,,MONDO:0004963,T-cell acute lymphoblastic leukemia,
+BMGC_DS12576,BMG_DS041635,,"Gaucher Disease, Type 1",Gaucher Disease,,,,,,C1961835,D005776,230800,MONDO:0009265,Gaucher disease type I,
+BMGC_DS12577,BMG_DS041641,,Spinocerebellar Ataxia 10,,,,,,,C1963674,C566874,603516,MONDO:0011330,spinocerebellar ataxia type 10,
+BMGC_DS12578,BMG_DS041652,,"ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS",,,,,DOID:0111932,severe congenital encephalopathy due to MECP2 mutation,C1968556,,300673,MONDO:0010397,severe neonatal-onset encephalopathy with microcephaly,
+BMGC_DS12579,BMG_DS041653,,"Xeroderma Pigmentosum, Type G-Cockayne Syndrome",,,,,,,C1968561,C566879,,MONDO:0800314,"xeroderma pigmentosum, type G/Cockayne syndrome",
+BMGC_DS12580,BMG_DS041654,,Respiratory Distress Syndrome In Premature Infants,,,,,,,C1968593,C566881,267450,MONDO:0009971,respiratory distress syndrome in premature infants,
+BMGC_DS12581,BMG_DS041655,,"Surfactant Metabolism Dysfunction, Pulmonary, 1",,,,,,,C1968602,C566882,265120,MONDO:0009929,"surfactant metabolism dysfunction, pulmonary, 1",
+BMGC_DS12582,BMG_DS041656,,"Osteopetrosis, Autosomal Recessive 5",,,,,,,C1968603,C566883,259720,MONDO:0009817,autosomal recessive osteopetrosis 5,
+BMGC_DS12583,BMG_DS041657,,"Microphthalmia With Hyperopia, Retinal Degeneration, Macrophakia, And Dental Anomalies",,,,,,,C1968637,C566884,251700,MONDO:0009632,"microphthalmia with hyperopia, retinal degeneration, macrophakia, and dental anomalies",
+BMGC_DS12584,BMG_DS041658,,,,,,,,,C1968668,,246300,MONDO:0009518,"leprosy, susceptibility to, 3",
+BMGC_DS12585,BMG_DS041659,,,,,,,DOID:3261,hyper IgE recurrent infection syndrome 1,C1968689,,,,,
+BMGC_DS12586,BMG_DS041661,,Glycogen Storage Disease IIIA,,,,,,,C1968739,C566889,,,,
+BMGC_DS12587,BMG_DS041662,,Glycogen Storage Disease IIIB,,,,,,,C1968740,C566890,,,,
+BMGC_DS12588,BMG_DS041663,,Glycogen Storage Disease IIIC,,,,,,,C1968741,C566891,,,,
+BMGC_DS12589,BMG_DS041666,,"Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement",,,,,,,C1968748,C566895,,,,
+BMGC_DS12590,BMG_DS041668,,"MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES",,,,,,,C1968782,,190020;218040,MONDO:0800299,"myopathy, congenital, with excess of muscle spindles",
+BMGC_DS12591,BMG_DS041669,,"Plasminogen Deficiency, Type I",,,,,DOID:0111592,plasminogen deficiency type I,C1968804,C566897,217090,MONDO:0009009,hypoplasminogenemia,
+BMGC_DS12592,BMG_DS041672,,"Microphthalmia, Isolated, with Coloboma 5",,,,,,,C1968843,C566899,611638,MONDO:0012709,"microphthalmia, isolated, with coloboma 5",
+BMGC_DS12593,BMG_DS041673,,"Primary Lateral Sclerosis, Adult, 1",,,,,,,C1968845,C566900,611637,MONDO:0012708,"primary lateral sclerosis, adult, 1",
+BMGC_DS12594,BMG_DS041674,,"Febrile Convulsions, Familial, 9",,,,,,,C1968846,C566901,611634,MONDO:0012707,familial febrile seizures 9,
+BMGC_DS12595,BMG_DS041675,,"Epilepsy, Familial Temporal Lobe, 4",,,,,,,C1968847,C566902,611631,MONDO:0012706,familial temporal lobe epilepsy 4,
+BMGC_DS12596,BMG_DS041676,,"Epilepsy, Familial Mesial Temporal Lobe",,,,,,,C1968848,C566903,611630,MONDO:0012705,familial temporal lobe epilepsy 3,
+BMGC_DS12597,BMG_DS041677,,"Preauricular Tag, Isolated, Autosomal Dominant, 1",,,,,,,C1968893,C566904,610420,MONDO:0012486,"preauricular tag, isolated, autosomal dominant, 1",
+BMGC_DS12598,BMG_DS041678,,,,,,,,,C1968924,,,MONDO:0800416,"autism, susceptibility to, 1",
+BMGC_DS12599,BMG_DS041679,,,,,,,,,C1968949,,,MONDO:0019719,congenital anomaly of kidney and urinary tract,
+BMGC_DS12600,BMG_DS041680,,"CARDIOMYOPATHY, DILATED, 1X",,,,,,,C1969024,,607440;611615,MONDO:0012704,dilated cardiomyopathy 1X,
+BMGC_DS12601,BMG_DS041681,,Lissencephaly 3,,,,,DOID:0112232,lissencephaly 3,C1969029,C566908,,MONDO:0015148,lissencephaly type 3,
+BMGC_DS12602,BMG_DS041684,,"Cataract, Autosomal Dominant, Multiple Types 1",,,,,,,C1969032,C566909,,,,
+BMGC_DS12603,BMG_DS041685,,"Renal Tubular Acidosis, Distal, With Hemolytic Anemia",,,,,,,C1969038,C566910,,,,
+BMGC_DS12604,BMG_DS041686,,"Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology",,,,,,,C1969039,C566911,,,,
+BMGC_DS12605,BMG_DS041687,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2M",,,,,,,C1969040,,611588,MONDO:0012699,autosomal recessive limb-girdle muscular dystrophy type 2M,
+BMGC_DS12606,BMG_DS041688,,OTOSCLEROSIS 7,,,,,DOID:0060925,otosclerosis 7,C1969044,,611572,MONDO:0012697,otosclerosis 7,
+BMGC_DS12607,BMG_DS041689,,OTOSCLEROSIS 4,,,,,DOID:0060923,otosclerosis 4,C1969046,,611571,MONDO:0012696,otosclerosis 4,
+BMGC_DS12608,BMG_DS041690,,"MECKEL SYNDROME, TYPE 5",,,,,,,C1969052,,610937;611561,MONDO:0012695,"Meckel syndrome, type 5",
+BMGC_DS12609,BMG_DS041691,,JOUBERT SYNDROME 7,,,,,,,C1969053,,611560;610937,MONDO:0012694,Joubert syndrome 7,
+BMGC_DS12610,BMG_DS041692,,"Glycogen Storage Disease 0, Muscle",,,,,,,C1969054,C566917,611556,MONDO:0012693,glycogen storage disease due to muscle and heart glycogen synthase deficiency,
+BMGC_DS12611,BMG_DS041693,,"Renal Tubular Acidosis, Distal, With Nephrocalcinosis, Short Stature, Mental Retardation, And Distinctive Facies",,,,,,,C1969055,C566918,611555,MONDO:0012692,"renal tubular acidosis, distal, with nephrocalcinosis, short stature, intellectual disability, and distinctive facies",
+BMGC_DS12612,BMG_DS041694,,LEOPARD SYNDROME 2,,,,,,,C1969056,,164760;611554,MONDO:0012691,LEOPARD syndrome 2,
+BMGC_DS12613,BMG_DS041695,,Noonan Syndrome 5,,,,,DOID:0060583,Noonan syndrome 5,C1969057,C548083,611553,MONDO:0012690,Noonan syndrome 5,
+BMGC_DS12614,BMG_DS041696,,Premature Ovarian Failure 5,,,,,,,C1969060,C566921,611548,MONDO:0012689,premature ovarian failure 5,
+BMGC_DS12615,BMG_DS041697,,"Cataract, Congenital Nuclear, Autosomal Recessive 3",,,,,,,C1969062,C566923,,,,
+BMGC_DS12616,BMG_DS041698,,,,,,,,,C1969063,,611543,MONDO:0012687,familial cavitary optic disk anomaly,
+BMGC_DS12617,BMG_DS041700,,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 12",,,,,,,C1969081,C566925,611528,MONDO:0012684,arrhythmogenic right ventricular dysplasia 12,
+BMGC_DS12618,BMG_DS041701,,Pontocerebellar Hypoplasia Type 6,,,,,DOID:0060275,pontocerebellar hypoplasia type 6,C1969084,C548074,611523,MONDO:0012683,pontocerebellar hypoplasia type 6,
+BMGC_DS12619,BMG_DS041702,,Tyrosine Kinase 2 Deficiency,,,,,DOID:0111989,immunodeficiency 35,C1969086,C566928,611521,MONDO:0012682,immunodeficiency 35,
+BMGC_DS12620,BMG_DS041704,,NEPHRONOPHTHISIS 7,,,,,,,C1969092,,608539;611498,MONDO:0012680,nephronophthisis 7,
+BMGC_DS12621,BMG_DS041705,,"Osteopetrosis, Autosomal Recessive 6",,,,,,,C1969093,C566931,611497,MONDO:0012679,autosomal recessive osteopetrosis 6,
+BMGC_DS12622,BMG_DS041706,,"Atrial Fibrillation, Familial, 5",,,,,,,C1969099,C566932,611494,MONDO:0012678,"atrial fibrillation, familial, 5",
+BMGC_DS12623,BMG_DS041707,,"Osteopetrosis, Autosomal Recessive 4",,,,,,,C1969106,C566933,611490,MONDO:0012676,autosomal recessive osteopetrosis 4,
+BMGC_DS12624,BMG_DS041710,,GALLBLADDER DISEASE 4,,,,,,,C1969115,,605460;611465,,,
+BMGC_DS12625,BMG_DS041711,,"PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED",,,,,,,C1969342,,600799;178600,,,
+BMGC_DS12626,BMG_DS041712,,"Pulmonary Hypertension, Primary, Fenfluramine-Associated",Familial Primary Pulmonary Hypertension,,,,,,C1969343,D065627,,,,
+BMGC_DS12627,BMG_DS041714,,Trifunctional Protein Deficiency With Myopathy And Neuropathy,,,,,DOID:0111277,mitochondrial trifunctional protein deficiency,C1969443,C566945,,MONDO:0012172,mitochondrial trifunctional protein deficiency,
+BMGC_DS12628,BMG_DS041718,,,,,,,,,C1969562,,156200,MONDO:0007974,"intellectual disability, autosomal dominant 1",
+BMGC_DS12629,BMG_DS041721,,"DEAFNESS, AUTOSOMAL RECESSIVE 63",,,,,,,C1969621,,611451;612414,MONDO:0012670,autosomal recessive nonsyndromic hearing loss 63,
+BMGC_DS12630,BMG_DS041722,703541007,Neurofibromatosis type 1-like syndrome,,,,,DOID:0070484,Legius syndrome,C1969623,,611431,MONDO:0012669,Legius syndrome,Legius syndrome | Neurofibromatosis type 1-like syndrome (disorder) | NFLS - neurofibromatosis type 1-like syndrome | Neurofibromatosis type 1-like syndrome
+BMGC_DS12631,BMG_DS041724,,"Cardiomyopathy, Dilated, 1w",,,,,,,C1969639,C566954,611407,MONDO:0012667,dilated cardiomyopathy 1W,
+BMGC_DS12632,BMG_DS041726,,"Cataract, Cortical, Juvenile-Onset",,,,,,,C1969644,C566955,,,,
+BMGC_DS12633,BMG_DS041727,,"Ataxia, Spastic, 3, Autosomal Recessive",,,,,,,C1969645,C566956,611390,MONDO:0012664,spastic ataxia 3,
+BMGC_DS12634,BMG_DS041730,,"Macular Degeneration, Age-Related, 9",,,,,,,C1969651,C566958,611378,MONDO:0012659,age related macular degeneration 9,
+BMGC_DS12635,BMG_DS041731,770406002,Brachydactyly type B2,,,,,,,C1969652,,611377,MONDO:0012658,brachydactyly type B2,Brachydactyly type B2 (disorder) | Brachydactyly type B2
+BMGC_DS12636,BMG_DS041732,,MUNGAN SYNDROME,,,,,,,C1969653,,606462;611376,MONDO:0012657,Mungan syndrome,
+BMGC_DS12637,BMG_DS041733,,,,,,,,,C1969655,,611369,MONDO:0012656,lethal congenital contracture syndrome 3,
+BMGC_DS12638,BMG_DS041734,,"MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 4",,,,,DOID:0111327,juvenile myoclonic epilepsy 4,C1969656,,611364,MONDO:0012655,"myoclonic epilepsy, juvenile, susceptibility to, 4",
+BMGC_DS12639,BMG_DS041735,,Atrial Septal Defect 4,,,,,,,C1969657,C566963,611363,MONDO:0012654,atrial septal defect 4,
+BMGC_DS12640,BMG_DS041736,,,,,,,,,C1969710,,607373,MONDO:0011824,"autism, susceptibility to, 8",
+BMGC_DS12641,BMG_DS041737,,"Persistent Hyperplastic Primary Vitreous, Autosomal Recessive",,,,,,,C1969783,C566966,221900,MONDO:0009097,"persistent hyperplastic primary vitreous, autosomal recessive",
+BMGC_DS12642,BMG_DS041739,,"Muscular Dystrophy, Limb-Girdle, Type 2L",,,,,,,C1969785,C566968,611307,MONDO:0012652,autosomal recessive limb-girdle muscular dystrophy type 2L,
+BMGC_DS12643,BMG_DS041740,,"Ataxia, Spastic, 2, Autosomal Recessive",,,,,,,C1969796,C566969,611302,MONDO:0012651,spastic ataxia 2,
+BMGC_DS12644,BMG_DS041741,,"Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation",,,,,,,C1969799,C566970,611291,MONDO:0012650,Cernunnos-XLF deficiency,
+BMGC_DS12645,BMG_DS041742,,"Dystonia, Focal, Task-Specific",,,,,,,C1969807,C566973,611284,MONDO:0044871,"dystonia, focal, task-specific",
+BMGC_DS12646,BMG_DS041743,,Isobutyryl-CoA dehydrogenase deficiency,,,,,,,C1969809,C535541,611283,MONDO:0012648,isobutyryl-CoA dehydrogenase deficiency,
+BMGC_DS12647,BMG_DS041744,,,,,,,,,C1969810,,611277;607681,MONDO:0011891,"febrile seizures, familial, 8",
+BMGC_DS12648,BMG_DS041745,,"Glaucoma 1, Open Angle, H",,,,,,,C1969811,C566976,611276,MONDO:0012646,"obsolete glaucoma 1, open angle, H",
+BMGC_DS12649,BMG_DS041749,,,,,,,,,C1969893,,136630,MONDO:0007634,"intellectual disability, FRA12A type",
+BMGC_DS12650,BMG_DS041752,,Asphyxiating Thoracic Dystrophy 2,,,,,DOID:0110086,asphyxiating thoracic dystrophy 2,C1970005,C566982,611263,MONDO:0012644,asphyxiating thoracic dystrophy 2,
+BMGC_DS12651,BMG_DS041753,,"SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE",,,,,,,C1970009,,611252,MONDO:0012643,hereditary spastic paraplegia 32,
+BMGC_DS12652,BMG_DS041755,,"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J",,,,,,,C1970011,,609390;611228,MONDO:0012640,Charcot-Marie-Tooth disease type 4J,
+BMGC_DS12653,BMG_DS041757,,,,,,,,,C1970020,,611185,MONDO:0012636,"restless legs syndrome, susceptibility to, 6",
+BMGC_DS12654,BMG_DS041758,,"Congenital Disorder Of Glycosylation, Type IIH",,,,,DOID:0070260,congenital disorder of glycosylation type IIh,C1970021,C566987,611182,MONDO:0012635,COG8-congenital disorder of glycosylation,
+BMGC_DS12655,BMG_DS041759,,"Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility",,,,,,,C1970027,C566988,611174,MONDO:0012634,craniofacial dysplasia - osteopenia syndrome,
+BMGC_DS12656,BMG_DS041760,,,,,,,,,C1970028,,611162,MONDO:0021024,"malaria, susceptibility to",
+BMGC_DS12657,BMG_DS041763,,"Bpes, Type I, Autosomal Recessive",,,,,,,C1970106,C566222,,,,
+BMGC_DS12658,BMG_DS041764,,,,,,,,,C1970107,,108600,MONDO:0007164,spastic ataxia 1,
+BMGC_DS12659,BMG_DS041765,,AROMATASE EXCESS SYNDROME,,,,,,,C1970109,,139300;107910,MONDO:0007690,aromatase excess syndrome,
+BMGC_DS12660,BMG_DS041768,,"CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED",,,,,DOID:0111700,ankyrin-B-related cardiac arrhythmia,C1970119,,600919;106410,MONDO:0010958,"cardiac arrhythmia, ankyrin-B-related",
+BMGC_DS12661,BMG_DS041769,,"Angioma serpiginosum, autosomal dominant",,,,,,,C1970130,C536365,106050,MONDO:0007115,"angioma serpiginosum, autosomal dominant",
+BMGC_DS12662,BMG_DS041774,,Paroxysmal Nonkinesigenic Dyskinesia 2,,,,,DOID:0090047,paroxysmal nonkinesigenic dyskinesia 2,C1970149,C567001,611147,MONDO:0012629,paroxysmal nonkinesigenic dyskinesia 2,
+BMGC_DS12663,BMG_DS041776,,"MECKEL SYNDROME, TYPE 4",,,,,,,C1970161,,610142;611134,MONDO:0012626,"Meckel syndrome, type 4",
+BMGC_DS12664,BMG_DS041778,,Retinitis Pigmentosa 37,,,,,DOID:0110399,retinitis pigmentosa 37,C1970163,C567005,611131,MONDO:0012625,retinitis pigmentosa 37,
+BMGC_DS12665,BMG_DS041779,,"Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of",,,,,DOID:0112072,nuclear type mitochondrial complex I deficiency 20,C1970173,C567006,,,,
+BMGC_DS12666,BMG_DS041781,,,,,,,,,C1970179,,611107,MONDO:0012623,"intellectual disability, autosomal recessive 4",
+BMGC_DS12667,BMG_DS041782,,Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation,,,,,,,C1970180,C567009,611105,MONDO:0012622,leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome,
+BMGC_DS12668,BMG_DS041783,,"Deafness, Sensorineural, And Male Infertility",,,,,,,C1970187,C567010,611102,MONDO:0012621,deafness-infertility syndrome,
+BMGC_DS12669,BMG_DS041785,,,,,,,,,C1970193,,611097,MONDO:0012619,"intellectual disability, autosomal recessive 11",
+BMGC_DS12670,BMG_DS041786,,,,,,,,,C1970194,,611096,MONDO:0012618,"intellectual disability, autosomal recessive 10",
+BMGC_DS12671,BMG_DS041787,,,,,,,,,C1970195,,611095,MONDO:0012617,"intellectual disability, autosomal recessive 9",
+BMGC_DS12672,BMG_DS041788,,,,,,,,,C1970197,,611093,MONDO:0012615,"intellectual disability, autosomal recessive 7",
+BMGC_DS12673,BMG_DS041789,,,,,,,,,C1970198,,611092,MONDO:0012614,"intellectual disability, autosomal recessive 6",
+BMGC_DS12674,BMG_DS041790,,,,,,,,,C1970199,,611091,MONDO:0012613,"intellectual disability, autosomal recessive 5",
+BMGC_DS12675,BMG_DS041791,,,,,,,,,C1970200,,611090,MONDO:0012612,"intellectual disability, autosomal recessive 12",
+BMGC_DS12676,BMG_DS041792,,"Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy",,,,,DOID:0070511,"polyhydramnios, megalencephaly, and symptomatic epilepsy",C1970203,C567020,611087,MONDO:0012611,"polyhydramnios, megalencephaly, and symptomatic epilepsy",
+BMGC_DS12677,BMG_DS041793,,Inflammatory Bowel Disease 10,,,,,DOID:0110885,inflammatory bowel disease 10,C1970207,C567021,611081,MONDO:0012610,inflammatory bowel disease 10,
+BMGC_DS12678,BMG_DS041795,,"Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4",,,,,DOID:0111213,autosomal recessive distal hereditary motor neuronopathy 4,C1970211,C567023,611067,MONDO:0012608,"neuronopathy, distal hereditary motor, autosomal recessive 4",
+BMGC_DS12679,BMG_DS041796,,,,,,,,,C1970224,,611064,MONDO:0012607,"asthma-related traits, susceptibility to, 5",
+BMGC_DS12680,BMG_DS041798,,"Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen",,,,,,,C1970236,C567024,611040,MONDO:0012605,isolated microphthalmia 5,
+BMGC_DS12681,BMG_DS041799,,"Microphthalmia, Isolated 3",,,,,,,C1970237,C567025,,,,
+BMGC_DS12682,BMG_DS041800,,Episodic Kinesigenic Dyskinesia 2,,,,,DOID:0090054,episodic kinesigenic dyskinesia 2,C1970238,C567026,611031,MONDO:0012603,episodic kinesigenic dyskinesia 2,
+BMGC_DS12683,BMG_DS041801,,"DEAFNESS, AUTOSOMAL RECESSIVE, 24",,,,,,,C1970239,,611022;179410,MONDO:0012602,autosomal recessive nonsyndromic hearing loss 24,
+BMGC_DS12684,BMG_DS041802,,,,,,,,,C1970242,,611016,MONDO:0012601,"autism, susceptibility to, 10",
+BMGC_DS12685,BMG_DS041803,,,,,,,,,C1970243,,611015,MONDO:0012600,"autism, susceptibility to, 9",
+BMGC_DS12686,BMG_DS041806,,,,,,,,,C1970250,,610997,MONDO:0012597,"prostate cancer, hereditary, 9",
+BMGC_DS12687,BMG_DS041807,,Phosphoserine Aminotransferase Deficiency,,,,,,,C1970253,C567032,610992,MONDO:0012596,PSAT deficiency,
+BMGC_DS12688,BMG_DS041808,,,,,,,,,C1970254,,610988,MONDO:0012595,"leprosy, susceptibility to, 4",
+BMGC_DS12689,BMG_DS041809,,"Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress",,,,,,,C1970269,C567034,610978,MONDO:0012593,brain-lung-thyroid syndrome,
+BMGC_DS12690,BMG_DS041810,,Choreoathetosis And Congenital Hypothyroidism,,,,,,,C1970270,C567034,,,,
+BMGC_DS12691,BMG_DS041811,,"Tooth Agenesis, Selective, 3",,,,,,,C1970291,C567036,604625,MONDO:0011477,"tooth agenesis, selective, 3",
+BMGC_DS12692,BMG_DS041812,,"Progressive Familial Heart Block, Type Ib",,,,,DOID:0111076,progressive familial heart block type IB,C1970298,C567037,604559,MONDO:0011474,progressive familial heart block type IB,
+BMGC_DS12693,BMG_DS041813,,"Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation",,,,,,,C1970309,C567038,604278,MONDO:0011422,autosomal recessive proximal renal tubular acidosis,
+BMGC_DS12694,BMG_DS041815,,"Congenital Disorder Of Glycosylation, Type IIF",,,,,DOID:0070258,congenital disorder of glycosylation type IIf,C1970344,C567040,603585,MONDO:0011342,SLC35A1-congenital disorder of glycosylation,
+BMGC_DS12695,BMG_DS041816,,"Cataract, Posterior Polar, 4, With Microphthalmia And Neurodevelopmental Abnormalities",,,,,,,C1970386,C535344,,,,
+BMGC_DS12696,BMG_DS041817,,XFE Progeroid Syndrome,,,,,DOID:0060590,XFE progeroid syndrome,C1970416,C567043,610965,MONDO:0012590,XFE progeroid syndrome,
+BMGC_DS12697,BMG_DS041818,,PITT-HOPKINS SYNDROME,,,,,DOID:0060488,Pitt-Hopkins syndrome,C1970431,,610954;602272,MONDO:0012589,Pitt-Hopkins syndrome,
+BMGC_DS12698,BMG_DS041820,,"Coronary Artery Disease, Autosomal Dominant 2",,,,,,,C1970440,C567045,610947,MONDO:0012586,"coronary artery disease, autosomal dominant 2",
+BMGC_DS12699,BMG_DS041821,,,,,,,,,C1970441,,610938,MONDO:0012585,"coronary heart disease, susceptibility to, 7",
+BMGC_DS12700,BMG_DS041822,,,,,,,,,C1970455,,610927,MONDO:0012584,"systemic lupus erythematosus, susceptibility to, 9",
+BMGC_DS12701,BMG_DS041823,,"Surfactant Metabolism Dysfunction, Pulmonary, 3",,,,,,,C1970456,C567046,610921,MONDO:0012582,interstitial lung disease due to ABCA3 deficiency,
+BMGC_DS12702,BMG_DS041824,,"Osteogenesis imperfecta, type VIII",,,,,,,C1970458,C536049,610915,MONDO:0012581,osteogenesis imperfecta type 8,
+BMGC_DS12703,BMG_DS041826,,"Surfactant Metabolism Dysfunction, Pulmonary, 2",,,,,,,C1970470,C567048,610913,MONDO:0024465,"surfactant metabolism dysfunction, pulmonary, 2",
+BMGC_DS12704,BMG_DS041827,,"PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED",,,,,,,C1970472,,610910,MONDO:0012579,autoimmune pulmonary alveolar proteinosis,
+BMGC_DS12705,BMG_DS041831,,Branchiootorenal Syndrome 2,Branchio-Oto-Renal Syndrome,,,,,,C1970479,D019280,610896,MONDO:0012575,branchiootorenal syndrome 2,
+BMGC_DS12706,BMG_DS041832,,Vesicoureteral Reflux 2,,,,,,,C1970483,C567053,610878,MONDO:0012573,vesicoureteral reflux 2,
+BMGC_DS12707,BMG_DS041834,,"CILIARY DYSKINESIA, PRIMARY, 6",,,,,,,C1970506,,607421;610852,MONDO:0012571,primary ciliary dyskinesia 6,
+BMGC_DS12708,BMG_DS041837,,,,,,,,,C1970712,,610755,MONDO:0012552,multiple endocrine neoplasia type 4,
+BMGC_DS12709,BMG_DS041838,,,,,,,,,C1970723,,600156,MONDO:0010834,"Hirschsprung disease, susceptibility to, 5",
+BMGC_DS12710,BMG_DS041839,,"Tooth Agenesis, Selective, X-Linked, 1",,,,,,,C1970757,C567060,313500,MONDO:0010741,"tooth agenesis, selective, X-linked, 1",
+BMGC_DS12711,BMG_DS041842,,"Fabry Disease, Cardiac Variant",,,,,,,C1970820,C567062,,,,
+BMGC_DS12712,BMG_DS041843,,"Mental Retardation, X-Linked, Syndromic 14",,,,,,,C1970822,C567063,300676,MONDO:0010398,syndromic X-linked intellectual disability 14,
+BMGC_DS12713,BMG_DS041844,,Phosphoribosylpyrophosphate Synthetase Superactivity,,,,,DOID:0111260,phosphoribosylpyrophosphate synthetase superactivity,C1970827,C567064,300661,MONDO:0010395,phosphoribosylpyrophosphate synthetase superactivity,
+BMGC_DS12714,BMG_DS041845,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93",,,,,DOID:0112045,non-syndromic X-linked intellectual disability 93,C1970841,,300553;300659,MONDO:0010393,"intellectual disability, X-linked 93",
+BMGC_DS12715,BMG_DS041846,,Phosphoglycerate Kinase 1 Deficiency,,,,,DOID:0111933,phosphoglycerate kinase 1 deficiency,C1970848,C567067,300653,MONDO:0010392,glycogen storage disease due to phosphoglycerate kinase 1 deficiency,
+BMGC_DS12716,BMG_DS041847,,"Atypical Mycobacteriosis, Familial, X-Linked 2",,,,,DOID:0112000,immunodeficiency 34,C1970859,C567068,300645,MONDO:0010389,X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency,
+BMGC_DS12717,BMG_DS041848,,IMMUNODEFICIENCY 33,,,,,DOID:0112003,immunodeficiency 33,C1970879,,300248;300584;300636;300636,MONDO:0010386,immunodeficiency 33,
+BMGC_DS12718,BMG_DS041859,43339004,Potassium depletion,,,,,,,C1971021,,,,,Hypokalemia | Potassium depletion | K deficiency | Hypopotassemia syndrome | Hypokalemic syndrome | Hypokalaemic syndrome | Potassium deficiency | Hypokalaemia | Hypopotassaemia | Hypopotassemia | Hypopotassaemia syndrome | Hypokalemia (disorder)
+BMGC_DS12719,BMG_DS041954,428015005,Chlamydia trachomatis infection of genital structure,,,,,,,C1997322,,,,,Chlamydia trachomatis infection of genital structure (disorder) | Chlamydia trachomatis genital infection | Chlamydia trachomatis infection of genital structure
+BMGC_DS12720,BMG_DS041958,429589006,Left ventricular cardiac dysfunction,,,,,,,C1997351,,,,,Left ventricular cardiac dysfunction (disorder) | Left ventricular cardiac dysfunction
+BMGC_DS12721,BMG_DS041996,428783003,Osteomyelitis caused by Staphylococcus aureus,,,,,,,C1997728,,,,,Osteomyelitis caused by Staphylococcus aureus (disorder) | Osteomyelitis caused by Staphylococcus aureus
+BMGC_DS12722,BMG_DS042014,429735007,Citrin deficiency,,,,,,,C1997910,,,MONDO:0016602,citrin deficiency,Citrin deficiency (disorder) | Citrin deficiency | SLC25A13 related citrin deficiency | Solute carrier family 25 member 13 related citrin deficiency
+BMGC_DS12723,BMG_DS042157,196624002,Oesophageal reflux (& [without mention of oesophagitis]),,,,,,,C2004423,,,,,Esophageal reflux (& [without mention of esophagitis]) | Acid reflux | Oesophageal reflux (& [without mention of oesophagitis]) | Gastro-oesophageal reflux | Oesophageal reflux | Oesopheal reflux without mention of oesophagitis | Gastro-oesophageal reflux disease without oesophagitis | Gastro-esophageal reflux | Esopheal reflux without mention of esophagitis | Esophageal reflux | Gastro-esophageal reflux disease without esophagitis | Oesophageal reflux (& [without mention of oesophagitis]) (disorder)
+BMGC_DS12724,BMG_DS042159,82196007,Vascular insufficiency of intestine,,,,,,,C2004435,,,MONDO:0020675,ischemic bowel disorder,Vascular insufficiency of intestine | Ischemic bowel disease | Vascular insufficiency of the intestine | Intestinal ischemia | Ischemic disease of gut | Intestinal ischaemia | Ischaemic bowel disease | Ischaemic disease of gut | Vascular insufficiency of intestine (disorder)
+BMGC_DS12725,BMG_DS042256,,,,,,,DOID:5310,glycogen-rich clear cell breast carcinoma,C2012261,,,MONDO:0003390,glycogen-rich clear cell breast carcinoma,
+BMGC_DS12726,BMG_DS042282,,,,,,,DOID:5531,ovarian squamous cell carcinoma,C2019443,,,MONDO:0003494,ovarian squamous cell carcinoma,
+BMGC_DS12727,BMG_DS042286,,"Stickler syndrome, type 1",,,,,,,C2020284,C537492,108300,MONDO:0007160,Stickler syndrome type 1,
+BMGC_DS12728,BMG_DS042308,,Group B Streptococcal Infection,Streptococcal Infections,,,,,,C2020625,D013290,,MONDO:0700218,group B streptococcal infection,
+BMGC_DS12729,BMG_DS042349,,,,,,,DOID:0081313,primary diffuse large B-cell lymphoma of the central nervous system,C2026186,,,MONDO:0017596,diffuse large B-cell lymphoma of the central nervous system,
+BMGC_DS12730,BMG_DS042351,,,,,,,,,C2026514,,,MONDO:0010247,X-linked cerebral adrenoleukodystrophy,
+BMGC_DS12731,BMG_DS042352,,Haemophilus influenzae Type b Infection,Haemophilus Infections,,,,,,C2028293,D006192,,MONDO:0006926,haemophilus infectious disease,
+BMGC_DS12732,BMG_DS042357,,,,,,,DOID:5741,pancreatic vasoactive intestinal peptide producing tumor,C2033037,,,MONDO:0003622,pancreatic vasoactive intestinal peptide producing tumor,
+BMGC_DS12733,BMG_DS042390,267434003,Mixed hyperlipidemia (disorder),,,,,,,C2047520,,,,,Mixed hyperlipidaemia | Multiple-type hyperlipidaemia | Multiple-type hyperlipidemia | Mixed hyperlipidemia | Mixed hyperlipidemia (disorder)
+BMGC_DS12734,BMG_DS042400,,,,,,,DOID:9550,indolent plasma cell myeloma,C2049069,,,,,
+BMGC_DS12735,BMG_DS042403,,,,,,,,,C2051831,,169300,MONDO:0008213,pectus excavatum,
+BMGC_DS12736,BMG_DS042428,,,,,,,DOID:4086,testicular germ cell tumor non-seminomatous,C2057625,,,MONDO:0006447,testicular non-seminomatous germ cell tumor,
+BMGC_DS12737,BMG_DS042432,,,,,,,,,C2062367,,,MONDO:0018060,congenital fibrinogen deficiency,
+BMGC_DS12738,BMG_DS042433,720459002,Hypercortisolism due to macronodular adrenal hyperplasia,,,,,DOID:0111622,ACTH-independent macronodular adrenal hyperplasia,C2062388,,,MONDO:0009049,Cushing syndrome due to macronodular adrenal hyperplasia,Hypercortisolism due to macronodular adrenal hyperplasia (disorder) | Hypercortisolism due to macronodular adrenal hyperplasia | Cushing syndrome due to macronodular adrenal hyperplasia
+BMGC_DS12739,BMG_DS042442,838353009,Acute pyelonephritis caused by bacterium,,,,,,,C2062473,,,,,Acute pyelonephritis caused by bacterium | Acute pyelonephritis caused by bacterium (disorder) | Acute bacterial pyelonephritis
+BMGC_DS12740,BMG_DS042454,1010634002,Pneumonia caused by Acinetobacter,,,,,,,C2063075,,,,,Pneumonia caused by Acinetobacter (disorder) | Acinetobacter pneumonia | Pneumonia caused by Acinetobacter
+BMGC_DS12741,BMG_DS042466,,,,,,,DOID:7234,mucinous cystadenocarcinoma of pancreas,C2063873,,,MONDO:0004156,pancreatic mucinous cystadenocarcinoma,
+BMGC_DS12742,BMG_DS042469,,,,,,,DOID:3254,bile duct rhabdomyosarcoma,C2064434,,,MONDO:0002577,extrahepatic bile duct rhabdomyosarcoma,
+BMGC_DS12743,BMG_DS042584,,"Postoperative Pain, Chronic","Pain, Postoperative",,,,,,C2074900,D010149,,,,
+BMGC_DS12744,BMG_DS042590,442696006,Influenza due to Influenza A virus subtype H1N1,,,,,,,C2076600,,,,,Influenza A (H1N1) | Influenza caused by Influenza A virus subtype H1N1 | Influenza caused by Influenza A virus subtype H1N1 (disorder)
+BMGC_DS12745,BMG_DS042724,,,,,,,,,C2169806,,,MONDO:0002420,tic disorder,
+BMGC_DS12746,BMG_DS042802,,,,,,,DOID:4064,bile duct sarcoma,C2205442,,,MONDO:0024658,extrahepatic bile duct sarcoma,
+BMGC_DS12747,BMG_DS042808,,,,,,,,,C2212006,,,MONDO:0003795,ovarian small cell carcinoma,
+BMGC_DS12748,BMG_DS042926,,"Brucellosis, Pulmonary",Brucellosis,,,,,,C2231324,D002006,,,,
+BMGC_DS12749,BMG_DS042978,,,,,,,DOID:684,hepatocellular carcinoma,C2239176,,114550,MONDO:0007256,hepatocellular carcinoma,
+BMGC_DS12750,BMG_DS042988,,"DEAFNESS, AUTOSOMAL RECESSIVE 74",,,,,,,C2239351,,613718;613719,MONDO:0013386,autosomal recessive nonsyndromic hearing loss 74,
+BMGC_DS12751,BMG_DS042994,111253001,Infection of bone,,,,,,,C2242472,,,,,Infection of bone | Bone infection | Infection of bone (disorder)
+BMGC_DS12752,BMG_DS043002,,Phantosmia,Olfaction Disorders,,,,,,C2242552,D000857,,,,
+BMGC_DS12753,BMG_DS043004,,,,,,,,,C2242577,,,MONDO:0019771,oromandibular dystonia,
+BMGC_DS12754,BMG_DS043005,,Cardio-Renal Syndrome,Cardio-Renal Syndrome,,,,,,C2242703,D059347,,MONDO:0044079,cardio-renal syndrome,
+BMGC_DS12755,BMG_DS043008,200773006;24079001,Besnier's prurigo,,EC91.1,Atopic prurigo,L20.0,,,C2242769,,,,,Besnier's prurigo | Besnier's prurigo (disorder) | Besnier prurigo | Atopic dermatitis | Atopic eczema | Disseminated neurodermatitis | Atopic dermatitis (disorder) | AD - Atopic dermatitis | Constitutional eczema
+BMGC_DS12756,BMG_DS043031,201232004;201234003;87373006;419093005;254677004,Trichilemmal cyst,,,,,,,C2266788,,609649,MONDO:0012328,trichilemmal cyst,Trichilemmal cyst | Trichilemmal cyst (disorder) | Sebaceous cyst | Steatocystoma | Wen | Pilar cyst | Trichilemmal cyst | Sebaceous cyst (morphologic abnormality) | Keratinising cyst | Keratinizing cyst | Keratinous cyst | Steatoma | Trichilemmal cyst (morphologic abnormality) | Trichilemmal cyst | Pilar cyst | Trichilemmal cyst | Follicular isthmus cyst | Pilar cyst | Isthmus catagen cyst | Trichilemmal cyst (disorder)
+BMGC_DS12757,BMG_DS043032,,,,,,,,,C2267227,,,MONDO:0005452,bulimia nervosa,
+BMGC_DS12758,BMG_DS043035,53917000;234419009;234576008;248693006,Chronic idiopathic neutropenia,,,,,,,C2267231,,,,,Chronic idiopathic neutropenia | Chronic idiopathic neutropenia (disorder) | Chronic idiopathic neutropenia | Chronic idiopathic neutropaenia | Chronic idiopathic neutropenia (disorder) | Chronic familial neutropaenia | Benign familial neutropaenia | Chronic familial neutropenia (disorder) | Benign familial neutropenia | Chronic familial neutropenia | Chronic idiopathic neutropenia | Idiopathic agranulocytosis | Chronic idiopathic neutropenia (disorder)
+BMGC_DS12759,BMG_DS043036,,Neonatal Hypotonia,Muscle Hypotonia,,,,,,C2267233,D009123,,,,
+BMGC_DS12760,BMG_DS043039,,,,,,,,,C2314896,,,MONDO:0018453,familial atypical multiple mole melanoma syndrome,
+BMGC_DS12761,BMG_DS043043,432788009,Pediatric failure to thrive,,,,,,,C2315100,,,,,Pediatric failure to thrive (disorder) | Paediatric failure to thrive | Pediatric failure to thrive
+BMGC_DS12762,BMG_DS043094,,Cryopyrin-Associated Periodic Syndromes,Cryopyrin-Associated Periodic Syndromes,,,,,,C2316212,D056587,,MONDO:0016168,cryopyrin-associated periodic syndrome,
+BMGC_DS12763,BMG_DS043123,433146000,Chronic kidney disease stage 5,,,,,,,C2316810,,,MONDO:0004375,end stage renal failure,Chronic kidney disease stage 5 (disorder) | Chronic kidney disease stage 5 | CKD stage 5
+BMGC_DS12764,BMG_DS043131,,Fetal Pyelectasis,Pyelectasis,,,,,,C2317073,D058536,,,,
+BMGC_DS12765,BMG_DS043157,,,,,,,,,C2347126,,,MONDO:0019124,microscopic polyangiitis,
+BMGC_DS12766,BMG_DS043159,,Short Qt Syndrome,,,,,,,C2348199,C580439,,MONDO:0000453,short QT syndrome,
+BMGC_DS12767,BMG_DS043161,,Acute Anterior Wall Myocardial Infarction,Anterior Wall Myocardial Infarction,,,,,,C2349195,D056988,,,,
+BMGC_DS12768,BMG_DS043172,441658007,Pneumonia caused by Staphylococcus aureus,,,,,,,C2349530,,,,,Pneumonia caused by Staphylococcus aureus (disorder) | Pneumonia caused by Staphylococcus aureus
+BMGC_DS12769,BMG_DS043203,55875000;399329002,Tinea barbae,,,,,,,C2349994,,,MONDO:0000242,tinea barbae,"Tinea barbae | Tinea sycosis | Barbers' itch | Folliculitis barbae | Mycotic sycosis | Bacterial folliculitis | Dermatophytosis of beard | Sycosis vulgaris | Deep bacterial folliculitis | Sycosis barbae | Pseudofolliculitis barbae | Sycosis barbae, not parasitic | Barbers' rash | Tinea barbae (disorder) | Tinea barbae (disorder) | Tinea barbae | Tinea sycosis | Barbers' itch | Dermatophytosis of beard | Mycotic sycosis | Barbers' rash"
+BMGC_DS12770,BMG_DS043204,,Viral Croup,Croup,,,,,,C2350035,D003440,,,,
+BMGC_DS12771,BMG_DS043205,,Postintubation Croup,Croup,,,,,,C2350036,D003440,,,,
+BMGC_DS12772,BMG_DS043206,,"Clinically Isolated Syndrome, CNS Demyelinating",Demyelinating Diseases,,,,,,C2350037,D003711,,,,
+BMGC_DS12773,BMG_DS043209,,Polymorphic Reticulosis,"Granuloma, Lethal Midline",,,,,,C2350168,D006103,,,,
+BMGC_DS12774,BMG_DS043210,,Unilateral Nasal Obstruction,Nasal Obstruction,,,,,,C2350170,D015508,,,,
+BMGC_DS12775,BMG_DS043211,,Bilateral Nasal Obstruction,Nasal Obstruction,,,,,,C2350171,D015508,,,,
+BMGC_DS12776,BMG_DS043212,,Antley-Bixler Syndrome Phenotype,Antley-Bixler Syndrome Phenotype,,,,,,C2350233,D054882,,,,
+BMGC_DS12777,BMG_DS043214,,Lumbarsacral Spondylosis,Spondylosis,,,,,,C2350238,D055009,,,,
+BMGC_DS12778,BMG_DS043215,,"Osteoarthritis, Spine","Osteoarthritis, Spine",,,,,,C2350242,D055013,,MONDO:0006630,"osteoarthritis, spine",
+BMGC_DS12779,BMG_DS043218,,Chronic Lung Injury,Lung Injury,,,,,,C2350344,D055370,,,,
+BMGC_DS12780,BMG_DS043228,,Resorption Pulmonary Atelectasis,Pulmonary Atelectasis,,,,,,C2350822,D001261,,,,
+BMGC_DS12781,BMG_DS043229,,Contraction Pulmonary Atelectasis,Pulmonary Atelectasis,,,,,,C2350823,D001261,,,,
+BMGC_DS12782,BMG_DS043230,,Postoperative Pulmonary Atelectasis,Pulmonary Atelectasis,,,,,,C2350824,D001261,,,,
+BMGC_DS12783,BMG_DS043231,,Beryllium Disease,Berylliosis,,,,,,C2350873,D001607,,,,
+BMGC_DS12784,BMG_DS043232,,Constrictive Bronchiolitis,Bronchiolitis Obliterans,,,,,,C2350875,D001989,,,,
+BMGC_DS12785,BMG_DS043233,,"Bronchiolitis, Exudative",Bronchiolitis Obliterans,,,,,,C2350876,D001989,,,,
+BMGC_DS12786,BMG_DS043234,,Focal Emphysema,Pulmonary Emphysema,,,,,,C2350878,D011656,,,,
+BMGC_DS12787,BMG_DS043235,,Tropical Eosinophilic Pneumonia,Pulmonary Eosinophilia,,,,,,C2350879,D011657,,,,
+BMGC_DS12788,BMG_DS043236,,"Bronchiolitis, Proliferative",Bronchiolitis Obliterans,,,,,,C2350988,D001989,,,,
+BMGC_DS12789,BMG_DS043242,,Pediatric Obesity,Pediatric Obesity,,,,,,C2362324,D063766,,,,
+BMGC_DS12790,BMG_DS043248,254118002;190861001;82236004,Vitamin D-resistant rickets,,,,E83.31,,,C2363065,,,,,Vitamin D-resistant rickets | Vitamin D-resistant rickets (disorder) | Familial x-linked hypophosphatemic vitamin D refractory rickets | Familial hypophosphatemia | Familial hypophosphatemic rickets | Familial hypophosphatemic osteomalacia | Vitamin D-resistant rickets | Vitamin D-resistant osteomalacia | Hereditary hypophosphatemia | X-linked vitamin D-resistant rickets | Familial vitamin D-resistant rickets | Familial hypophosphatemic bone disease | HPDR I - Hypophosphatemic vitamin D-resistant rickets | X-linked hypophosphatemic osteomalacia | X-linked hypophosphatemic rickets | Familial hypophosphataemic osteomalacia | Hereditary hypophosphataemia | X-linked hypophosphataemic osteomalacia | X-linked hypophosphataemic rickets | HPDR I - Hypophosphataemic vitamin D-resistant rickets | Familial hypophosphataemic bone disease | Familial hypophosphataemia | Familial hypophosphataemic rickets | Familial x-linked hypophosphataemic vitamin D refractory rickets | Familial x-linked hypophosphatemic vitamin D refractory rickets (disorder)
+BMGC_DS12791,BMG_DS043249,82236004,Vitamin D-resistant osteomalacia,,,,E83.31,,,C2363067,,,,,Familial x-linked hypophosphatemic vitamin D refractory rickets | Familial hypophosphatemia | Familial hypophosphatemic rickets | Familial hypophosphatemic osteomalacia | Vitamin D-resistant rickets | Vitamin D-resistant osteomalacia | Hereditary hypophosphatemia | X-linked vitamin D-resistant rickets | Familial vitamin D-resistant rickets | Familial hypophosphatemic bone disease | HPDR I - Hypophosphatemic vitamin D-resistant rickets | X-linked hypophosphatemic osteomalacia | X-linked hypophosphatemic rickets | Familial hypophosphataemic osteomalacia | Hereditary hypophosphataemia | X-linked hypophosphataemic osteomalacia | X-linked hypophosphataemic rickets | HPDR I - Hypophosphataemic vitamin D-resistant rickets | Familial hypophosphataemic bone disease | Familial hypophosphataemia | Familial hypophosphataemic rickets | Familial x-linked hypophosphataemic vitamin D refractory rickets | Familial x-linked hypophosphatemic vitamin D refractory rickets (disorder)
+BMGC_DS12792,BMG_DS043251,,Benign Rolandic Epilepsy,"Epilepsy, Rolandic",,,,,,C2363129,D019305,,,,
+BMGC_DS12793,BMG_DS043252,,,,,,,,,C2363142,,,MONDO:0019468,T-cell prolymphocytic leukemia,
+BMGC_DS12794,BMG_DS043256,,Myopic Astigmatism,Astigmatism,,,,,,C2363771,D001251,,,,
+BMGC_DS12795,BMG_DS043257,,,,,,,,,C2363903,,,MONDO:0016705,angiocentric glioma,
+BMGC_DS12796,BMG_DS043259,233947005,Chronic thromboembolic pulmonary hypertension,,,,I27.24,,,C2363973,,,,,Thromboembolic pulmonary hypertension | Thromboembolic pulmonary hypertension (disorder) | Chronic thromboembolic pulmonary hypertension
+BMGC_DS12797,BMG_DS043270,,Systemic sclerosis [scleroderma],,,,M34,,,C2364016,,,,,
+BMGC_DS12798,BMG_DS043283,439702007,Hereditary protein S deficiency,,,,,,,C2584611,,,MONDO:0019144,hereditary thrombophilia due to congenital protein S deficiency,Hereditary protein S deficiency (disorder) | Hereditary protein S deficiency
+BMGC_DS12799,BMG_DS043284,,"Thrombophilia, hereditary",,,,,,,C2584620,C540694,,MONDO:0100240,inherited thrombophilia,
+BMGC_DS12800,BMG_DS043296,439145006,Congenital hypofibrinogenemia,,,,,,,C2584774,,202400,MONDO:0008737,congenital afibrinogenemia,Congenital hypofibrinogenemia (disorder) | Congenital hypofibrinogenemia | Congenital hypofibrinogenaemia
+BMGC_DS12801,BMG_DS043308,267532001;30577005,Qualitative platelet disorder,,,,,,,C2585231,,,,,Qualitative platelet disorder (disorder) | Qualitative platelet defect | Qualitative platelet disorder | Qualitative platelet disorder | Thromboasthenia | Qualitative platelet disorder (disorder)
+BMGC_DS12802,BMG_DS043340,439699000,Hereditary antithrombin III deficiency,,,,,,,C2586031,,,,,Hereditary antithrombin III deficiency (disorder) | Hereditary antithrombin III deficiency
+BMGC_DS12803,BMG_DS043352,61582004,Allergic rhinitis (disorder),,,,,,,C2607914,,,MONDO:0011786,allergic rhinitis,Allergic rhinitis | Allergic rhinitis due to allergen | Allergic rhinitis (disorder) | AR - Allergic rhinitis | Atopic rhinitis
+BMGC_DS12804,BMG_DS043353,,"Carney Complex, Type 1",Carney Complex,,,,DOID:0050471,Carney complex,C2607929,D056733,160980,MONDO:0008057,"Carney complex, type 1",
+BMGC_DS12805,BMG_DS043356,162342008,Unilateral deafness,,,,,,,C2607947,,125000,MONDO:0007426,"deafness, unilateral",Unilateral deafness | Unilateral deafness (situation)
+BMGC_DS12806,BMG_DS043358,201153004;53593008,Folliculitis decalvans,,ED70.50,Folliculitis decalvans,L66.2,,,C2608043,,MTHU044513,MONDO:0018103,Quinquaud's folliculitis decalvans,Folliculitis decalvans | Folliculitis decalvans (disorder) | Folliculitis decalvans | Folliculitis decalvans (disorder) | Folliculitis depilans
+BMGC_DS12807,BMG_DS043359,,,,,,,,,C2608045,,,MONDO:0003073,trilateral retinoblastoma,
+BMGC_DS12808,BMG_DS043360,,,,,,,,,C2608055,,,MONDO:0003008,hereditary renal cell carcinoma,
+BMGC_DS12809,BMG_DS043361,,"Renal Hypoplasia, Isolated",,,,,,,C2608080,C537168,,,,
+BMGC_DS12810,BMG_DS043362,,"Cholestasis, benign recurrent intrahepatic 2",,,,,DOID:0070232,benign recurrent intrahepatic cholestasis 2,C2608083,C535934,605479,MONDO:0011559,benign recurrent intrahepatic cholestasis type 2,
+BMGC_DS12811,BMG_DS043363,,"Epidermolysis Bullosa, Junctional, Localisata Variant",,,,,,,C2608084,C562639,619787,MONDO:0030750,"epidermolysis bullosa, junctional 4, intermediate",
+BMGC_DS12812,BMG_DS043364,,,,,,,,,C2608087,,608634,MONDO:0012080,"neuronopathy, distal hereditary motor, type 2B",
+BMGC_DS12813,BMG_DS043367,445187004,Antisynthetase syndrome,,,,,DOID:0080744,antisynthetase syndrome,C2609059,C537778,,MONDO:0019344,antisynthetase syndrome,Antisynthetase syndrome (disorder) | Antisynthetase syndrome
+BMGC_DS12814,BMG_DS043369,,Autoimmune Pancreatitis,Autoimmune Pancreatitis,,,,DOID:0040091,autoimmune pancreatitis,C2609129,D000081012,,MONDO:0015175,autoimmune pancreatitis,
+BMGC_DS12815,BMG_DS043373,,,,,,,,,C2609268,,600803,MONDO:0010939,low phospholipid associated cholelithiasis,
+BMGC_DS12816,BMG_DS043377,,,,,,,,,C2609414,,,MONDO:0002492,acute kidney failure,
+BMGC_DS12817,BMG_DS043379,,"Aortic Aneurysm, Familial Thoracic 6",,,,,,,C2673186,C567085,611788,MONDO:0012730,"aortic aneurysm, familial thoracic 6",
+BMGC_DS12818,BMG_DS043380,,"Erythrocytosis, Familial, 4",,,,,,,C2673187,C567086,611783,MONDO:0012729,"erythrocytosis, familial, 4",
+BMGC_DS12819,BMG_DS043381,,Brugada Syndrome 2,,,,,DOID:0110219,Brugada syndrome 2,C2673193,C567087,611777,MONDO:0012728,Brugada syndrome 2,
+BMGC_DS12820,BMG_DS043382,,"Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps",,,,,,,C2673195,C567088,611773,MONDO:0012726,autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome,
+BMGC_DS12821,BMG_DS043383,,LIPOPROTEIN GLOMERULOPATHY,,,,,,,C2673196,,107741;611771,MONDO:0012725,lipoprotein glomerulopathy,
+BMGC_DS12822,BMG_DS043384,,Familial Cold Autoinflammatory Syndrome 2,,,,,DOID:0090063,familial cold autoinflammatory syndrome 2,C2673198,C567090,611762,MONDO:0012724,familial cold autoinflammatory syndrome 2,
+BMGC_DS12823,BMG_DS043386,,Brain Tumor-Polyposis Syndrome 2,,,,,,,C2673218,C566778,,,,
+BMGC_DS12824,BMG_DS043387,,,,,,,DOID:0111446,progressive myoclonus epilepsy 3,C2673257,,611726,MONDO:0012721,progressive myoclonic epilepsy type 3,
+BMGC_DS12825,BMG_DS043388,,"KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY",,,,,,,C2673266,,176801;611722,MONDO:0012720,Krabbe disease due to saposin A deficiency,
+BMGC_DS12826,BMG_DS043389,,"Mucolipidosis III Alpha Beta, Atypical",,,,,,,C2673375,C567099,,,,
+BMGC_DS12827,BMG_DS043390,,Mucolipidosis II Alpha Beta,,,,,,,C2673377,C567100,252500,MONDO:0009650,mucolipidosis type II,
+BMGC_DS12828,BMG_DS043391,,"Hypophosphatasia, Perinatal Lethal",,,,,,,C2673477,C567107,,MONDO:0016605,perinatal lethal hypophosphatasia,
+BMGC_DS12829,BMG_DS043393,,Hypergonadotropic Hypogonadism And Partial Alopecia,,,,,,,C2673480,C567109,241090,MONDO:0009420,primary hypergonadotropic hypogonadism-partial alopecia syndrome,
+BMGC_DS12830,BMG_DS043394,,"Leydig Cell Hypoplasia, Type II",,,,,DOID:0112259,Leydig cell hypoplasia,C2673497,C562567,,,,
+BMGC_DS12831,BMG_DS043395,,,,,,,,,C2673520,,612635,MONDO:0012971,"microvascular complications of diabetes, susceptibility to, 7",
+BMGC_DS12832,BMG_DS043396,,"Dystonia, Dopa-Responsive, With Or Without Hyperphenylalaninemia, Autosomal Recessive",,,,,,,C2673535,C537537,605407,MONDO:0011551,TH-deficient dopa-responsive dystonia,
+BMGC_DS12833,BMG_DS043397,,Combined Cellular And Humoral Immune Defects With Granulomas,,,,,DOID:0112253,combined cellular and humoral immune defects with granulomas,C2673536,C567115,233650,MONDO:0009306,combined immunodeficiency with skin granulomas,
+BMGC_DS12834,BMG_DS043400,,"Epidermolysis Bullosa Dystrophica, Autosomal Recessive, Localisata Variant",,,,,,,C2673611,C567121,,,,
+BMGC_DS12835,BMG_DS043401,,"Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive",,,,,,,C2673612,C567122,,,,
+BMGC_DS12836,BMG_DS043402,,"Hypothyroidism, Congenital, Nongoitrous, 5",,,,,,,C2673630,C567123,225250,MONDO:0009154,"hypothyroidism, congenital, nongoitrous, 5",
+BMGC_DS12837,BMG_DS043404,,Combined Saposin Deficiency,,,,,DOID:0111330,combined saposin deficiency,C2673635,C567125,611721,MONDO:0012719,combined PSAP deficiency,
+BMGC_DS12838,BMG_DS043405,,Combined Oxidative Phosphorylation Deficiency 5,,,,,DOID:0111473,combined oxidative phosphorylation deficiency 5,C2673642,C567126,611719,MONDO:0012718,hypotonia with lactic acidemia and hyperammonemia,
+BMGC_DS12839,BMG_DS043406,,"Hypomagnesemia 4, Renal",,,,,,,C2673648,C567127,611718,MONDO:0012717,renal hypomagnesemia 4,
+BMGC_DS12840,BMG_DS043407,,Spondyloepiphyseal Dysplasia-Brachydactyly and Distinctive Speech,,,,,DOID:0112287,spondyloepiphyseal dysplasia-brachydactyly and distinctive speech,C2673649,C567128,611717,MONDO:0012716,"spondyloepiphyseal dysplasia, Cantu type",
+BMGC_DS12841,BMG_DS043408,,,,,,,,,C2673676,,611706,MONDO:0012715,"migraine with or without aura, susceptibility to, 12",
+BMGC_DS12842,BMG_DS043409,,"Myopathy, Early-Onset, with Fatal Cardiomyopathy",,,,,,,C2673677,C567129,611705,MONDO:0012714,early-onset myopathy with fatal cardiomyopathy,
+BMGC_DS12843,BMG_DS043411,,Dystonia with Cerebellar Atrophy,,,,,,,C2673697,C567131,611694,MONDO:0012712,dystonia with cerebellar atrophy,
+BMGC_DS12844,BMG_DS043412,,Dibasic Amino Aciduria I,,,,,,,C2673736,C567132,222690,MONDO:0009108,hyperdibasic aminoaciduria type 1,
+BMGC_DS12845,BMG_DS043413,,"Deafness, Autosomal Recessive 1A",,,,,,,C2673759,C567134,220290,MONDO:0009076,autosomal recessive nonsyndromic hearing loss 1A,
+BMGC_DS12846,BMG_DS043414,,"Deafness, Digenic, Gjb2-Gjb6",,,,,,,C2673760,C567134,,,,
+BMGC_DS12847,BMG_DS043415,,"Deafness, Digenic, Gjb2-Gjb3",,,,,,,C2673761,C567134,,,,
+BMGC_DS12848,BMG_DS043417,,Ciliary Dyskinesia With Transposition Of Ciliary Microtubules,,,,,,,C2673817,C567137,215520,MONDO:0008985,ciliary dyskinesia with transposition of ciliary microtubules,
+BMGC_DS12849,BMG_DS043418,,BARDET-BIEDL SYNDROME 13,,,,,,,C2673873,,609883;615990,MONDO:0014441,Bardet-Biedl syndrome 13,
+BMGC_DS12850,BMG_DS043419,,Bardet-Biedl Syndrome 14,,,,,DOID:0110136,Bardet-Biedl syndrome 14,C2673874,C567141,615991,MONDO:0014442,Bardet-Biedl syndrome 14,
+BMGC_DS12851,BMG_DS043420,,,,,,,,,C2673883,,,MONDO:0017417,renal-hepatic-pancreatic dysplasia,
+BMGC_DS12852,BMG_DS043421,,Renal hepatic pancreatic dysplasia Dandy Walker cyst,,,,,DOID:0070121,Meckel syndrome 7,C2673885,C537756,267010,MONDO:0009966,NPHP3-related Meckel-like syndrome,
+BMGC_DS12853,BMG_DS043422,,"Anemia, Hypochromic Microcytic, With Iron Overload",,,,,,,C2673913,C567144,,MONDO:0000104,"anemia, hypochromic microcytic with iron overload",
+BMGC_DS12854,BMG_DS043423,,"Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive",,,,,,,C2673914,C567145,,,,
+BMGC_DS12855,BMG_DS043424,,"Amelogenesis Imperfecta, Hypomaturation Type, Iia1",,,,,,,C2673922,C567146,204700,MONDO:0008772,amelogenesis imperfecta type 2A1,
+BMGC_DS12856,BMG_DS043425,,"Amelogenesis Imperfecta, Type Ic",,,,,,,C2673923,C567147,204650,MONDO:0008770,amelogenesis imperfecta type 1C,
+BMGC_DS12857,BMG_DS043426,,,,,,,,,C2673946,,,MONDO:0044203,foveal hypoplasia,
+BMGC_DS12858,BMG_DS043427,,"Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma",,,,,,,C2674009,C536352,,,,
+BMGC_DS12859,BMG_DS043428,,R BINDER DEFICIENCY WITH LACTOFERRIN DEFICIENCY,,,,,,,C2674026,,193090,,,
+BMGC_DS12860,BMG_DS043432,,Inflammatory Bowel Disease 11,,,,,DOID:0110894,inflammatory bowel disease 11,C2674051,C567154,191390,MONDO:0008617,inflammatory bowel disease 11,
+BMGC_DS12861,BMG_DS043435,,,,,,,DOID:0111158,SADDAN,C2674173,,616482,MONDO:0014658,severe achondroplasia-developmental delay-acanthosis nigricans syndrome,
+BMGC_DS12862,BMG_DS043436,,"Spherocytosis, Type 1",,,,,,,C2674218,C567159,182900,MONDO:0008447,hereditary spherocytosis type 1,
+BMGC_DS12863,BMG_DS043437,,"SPHEROCYTOSIS, HEREDITARY, 2",,,,,DOID:0110917,hereditary spherocytosis type 2,C2674219,,616649,MONDO:0000913,hereditary spherocytosis type 2,
+BMGC_DS12864,BMG_DS043439,,"Neuromuscular Disease, Congenital, With Uniform Type 1 Fiber",,,,,,,C2674259,C567162,,,,
+BMGC_DS12865,BMG_DS043440,,"Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant",,,,,DOID:0111909,autosomal dominant thrombophilia due to protein C deficiency,C2674321,C567163,176860,MONDO:0008316,"thrombophilia due to protein C deficiency, autosomal dominant",
+BMGC_DS12866,BMG_DS043444,,"Seizures, intractable",,,,,,,C2674422,,MTHU021792,,,
+BMGC_DS12867,BMG_DS043447,,Palmoplantar Hyperkeratosis And True Hermaphroditism,,,,,,,C2674504,C567165,,,,
+BMGC_DS12868,BMG_DS043448,,"Aortic aneurysm, familial thoracic 3",,,,,,,C2674574,C537783,610168,MONDO:0012427,Loeys-Dietz syndrome 2,
+BMGC_DS12869,BMG_DS043451,,,,,,,,,C2674665,,612633,MONDO:0012969,"microvascular complications of diabetes, susceptibility to, 5",
+BMGC_DS12870,BMG_DS043453,,"Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant","Osteoarthropathy, Primary Hypertrophic",,,,,,C2674695,D010004,167100,MONDO:0008172,"hypertrophic osteoarthropathy, primary, autosomal dominant",
+BMGC_DS12871,BMG_DS043454,,"Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy",,,,,DOID:0111534,multicentric carpotarsal osteolysis syndrome,C2674705,C567171,166300,MONDO:0008152,multicentric carpo-tarsal osteolysis with or without nephropathy,
+BMGC_DS12872,BMG_DS043456,,RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER,,,,,,,C2674723,,614470,MONDO:0013767,autoimmune lymphoproliferative syndrome type 4,
+BMGC_DS12873,BMG_DS043457,,Myokymia 1,,,,,,,C2674766,C567174,,,,
+BMGC_DS12874,BMG_DS043458,,Faciocardiomelic Syndrome,,,,,,,C2674798,C567176,612731,MONDO:0012998,faciocardiomelic syndrome,
+BMGC_DS12875,BMG_DS043459,,,,,,,,,C2674838,,610251,MONDO:0012454,"alcohol sensitivity, acute",
+BMGC_DS12876,BMG_DS043460,,Chromosome 10q26 Deletion Syndrome,,,,,DOID:0060390,distal 10q deletion syndrome,C2674937,C567182,609625,MONDO:0012315,distal 10q deletion syndrome,
+BMGC_DS12877,BMG_DS043461,,Chromosome 3q29 Deletion Syndrome,,,,,DOID:0060419,chromosome 3q29 microdeletion syndrome,C2674949,C567184,609425,MONDO:0012269,chromosome 3q29 microdeletion syndrome,
+BMGC_DS12878,BMG_DS043462,,"Dandy-Walker Malformation With Occipital Cephalocele, Autosomal Dominant",,,,,,,C2674987,C567185,609222,MONDO:0012218,"dandy-walker malformation with occipital cephalocele, autosomal dominant",
+BMGC_DS12879,BMG_DS043463,,Mullerian Aplasia and Hyperandrogenism,,,,,DOID:0111526,Mullerian aplasia and hyperandrogenism,C2675014,C567186,158330,MONDO:0008019,mullerian aplasia and hyperandrogenism,
+BMGC_DS12880,BMG_DS043465,,Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus,,,,,,,C2675066,C567188,,,,
+BMGC_DS12881,BMG_DS043468,,,,,,,,,C2675112,,612628,MONDO:0012966,"microvascular complications of diabetes, susceptibility to, 4",
+BMGC_DS12882,BMG_DS043469,,,,,,,,,C2675128,,612634,MONDO:0012970,"microvascular complications of diabetes, susceptibility to, 6",
+BMGC_DS12883,BMG_DS043470,,"Hypospadias 3, Autosomal",,,,,,,C2675154,C567191,146450,MONDO:0007802,"hypospadias 3, autosomal",
+BMGC_DS12884,BMG_DS043471,,Arginine:Glycine Amidinotransferase Deficiency,,,,,,,C2675179,C567192,612718,MONDO:0012996,AGAT deficiency,
+BMGC_DS12885,BMG_DS043472,,Myopia 15,,,,,,,C2675180,C567193,612717,MONDO:0012995,"myopia 15, autosomal dominant",
+BMGC_DS12886,BMG_DS043474,,"Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis",,,,,,,C2675184,C567195,612714,MONDO:0012992,pancreatic insufficiency-anemia-hyperostosis syndrome,
+BMGC_DS12887,BMG_DS043475,,Kahrizi Syndrome,,,,,DOID:0050807,Kahrizi syndrome,C2675185,C567196,612713,MONDO:0012991,Kahrizi syndrome,
+BMGC_DS12888,BMG_DS043476,,LEBER CONGENITAL AMAUROSIS 13,,,,,,,C2675186,,608830;612712,MONDO:0012990,Leber congenital amaurosis 13,
+BMGC_DS12889,BMG_DS043477,,"Microcephaly, Primary Autosomal Recessive, 7",,,,,,,C2675187,C567198,612703,MONDO:0012989,"microcephaly 7, primary, autosomal recessive",
+BMGC_DS12890,BMG_DS043479,,"Polymicrogyria, Bilateral Occipital",,,,,,,C2675191,C567201,,,,
+BMGC_DS12891,BMG_DS043480,,"Spherocytosis, Type 5",,,,,,,C2675192,C567202,612690,MONDO:0012985,hereditary spherocytosis type 5,
+BMGC_DS12892,BMG_DS043481,,"Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract",,,,,,,C2675204,C567203,612674,MONDO:0012984,PHARC syndrome,
+BMGC_DS12893,BMG_DS043482,,Cone-Rod Dystrophy 12,,,,,DOID:0111019,cone-rod dystrophy 12,C2675210,C567206,612657,MONDO:0012983,cone-rod dystrophy 12,
+BMGC_DS12894,BMG_DS043483,,"Episodic Ataxia, Type 6",,,,,,,C2675211,C567207,612656,MONDO:0012982,episodic ataxia type 6,
+BMGC_DS12895,BMG_DS043484,,"Spherocytosis, Type 4",,,,,,,C2675212,C567208,612653,MONDO:0012981,hereditary spherocytosis type 4,
+BMGC_DS12896,BMG_DS043485,,Endocrine-Cerebroosteodysplasia,,,,,,,C2675227,C567210,612651,MONDO:0012980,endocrine-cerebro-osteodysplasia syndrome,
+BMGC_DS12897,BMG_DS043486,,"CILIARY DYSKINESIA, PRIMARY, 12",,,,,,,C2675228,,612650,MONDO:0012979,primary ciliary dyskinesia 12,
+BMGC_DS12898,BMG_DS043487,,"CILIARY DYSKINESIA, PRIMARY, 11",,,,,,,C2675229,,612649,MONDO:0012978,primary ciliary dyskinesia 11,
+BMGC_DS12899,BMG_DS043488,,"Deafness, Autosomal Recessive 1b",,,,,,,C2675235,C567213,612645,MONDO:0012977,autosomal recessive nonsyndromic hearing loss 1B,
+BMGC_DS12900,BMG_DS043489,,"Deafness, Autosomal Dominant 2B",,,,,,,C2675236,C567214,612644,MONDO:0012976,autosomal dominant nonsyndromic hearing loss 2B,
+BMGC_DS12901,BMG_DS043490,,"Deafness, Autosomal Dominant 3B",,,,,,,C2675237,C567215,612643,MONDO:0012975,autosomal dominant nonsyndromic hearing loss 3B,
+BMGC_DS12902,BMG_DS043491,,"Deafness, Autosomal Dominant 59",,,,,,,C2675238,C567216,612642,MONDO:0012974,autosomal dominant nonsyndromic hearing loss 59,
+BMGC_DS12903,BMG_DS043492,,Inflammatory Bowel Disease 26,,,,,DOID:0110901,inflammatory bowel disease 26,C2675249,C567217,612639,MONDO:0012973,inflammatory bowel disease 26,
+BMGC_DS12904,BMG_DS043496,,Duplication 15q11-q13 Syndrome,,,,,,,C2675336,C557830,608636,MONDO:0012081,15q11q13 microduplication syndrome,
+BMGC_DS12905,BMG_DS043497,,Chromosome 22q11.2 Microduplication Syndrome,,,,,DOID:0060436,chromosome 22q11.2 microduplication syndrome,C2675369,C567224,608363,MONDO:0012020,chromosome 22q11.2 microduplication syndrome,
+BMGC_DS12906,BMG_DS043498,,Capillary Malformation Without Arteriovenous Malformation,,,,,,,C2675370,C564254,,,,
+BMGC_DS12907,BMG_DS043499,,,,,,,,,C2675436,,614101,MONDO:0013575,plasma fibronectin deficiency,
+BMGC_DS12908,BMG_DS043500,,Desmoid Tumor Caused By Somatic Mutation,,,,,,,C2675440,C535944,,MONDO:0100168,desmoid tumor caused by somatic mutation,
+BMGC_DS12909,BMG_DS043502,,"Adenylate Kinase Deficiency, Hemolytic Anemia Due To",,,,,,,C2675459,C567228,612631,MONDO:0012967,hemolytic anemia due to adenylate kinase deficiency,
+BMGC_DS12910,BMG_DS043504,,Chromosome 15q26-Qter Deletion Syndrome,,,,,DOID:0060397,chromosome 15q26-qter deletion syndrome,C2675463,C567232,612626,MONDO:0012964,chromosome 15q26-qter deletion syndrome,
+BMGC_DS12911,BMG_DS043505,,,,,,,,,C2675470,,612624,MONDO:0012963,"microvascular complications of diabetes, susceptibility to, 3",
+BMGC_DS12912,BMG_DS043506,,,,,,,,,C2675471,,612623,MONDO:0012962,"microvascular complications of diabetes, susceptibility to, 2",
+BMGC_DS12913,BMG_DS043508,,,,,,,,,C2675473,,612621,MONDO:0012960,"intellectual disability, autosomal dominant 5",
+BMGC_DS12914,BMG_DS043511,,,,,,,,,C2675477,,612595,MONDO:0012957,"multiple sclerosis, susceptibility to, 3",
+BMGC_DS12915,BMG_DS043515,,,,,,,,,C2675481,,612591,MONDO:0012953,"colorectal cancer, susceptibility to, 10",
+BMGC_DS12916,BMG_DS043520,,Chromosome 6pter-P24 Deletion Syndrome,,,,,DOID:0060422,chromosome 6pter-p24 deletion syndrome,C2675486,C567239,612582,MONDO:0012948,chromosome 6pter-p24 deletion syndrome,
+BMGC_DS12917,BMG_DS043521,,,,,,,,,C2675487,,612581,MONDO:0012947,"intellectual disability, autosomal dominant 4",
+BMGC_DS12918,BMG_DS043522,,,,,,,,,C2675488,,612580,MONDO:0012946,"intellectual disability, autosomal dominant 3",
+BMGC_DS12919,BMG_DS043523,,AMYOTROPHIC LATERAL SCLEROSIS 11,,,,,DOID:0060202,amyotrophic lateral sclerosis type 11,C2675491,,612577;609390,MONDO:0012945,amyotrophic lateral sclerosis type 11,
+BMGC_DS12920,BMG_DS043524,,Split-Hand-Foot Malformation With Long Bone Deficiency 3,,,,,,,C2675492,C567245,612576,MONDO:0012944,"chromosome 17P13.3, telomeric, duplication syndrome",
+BMGC_DS12921,BMG_DS043525,,Retinitis Pigmentosa 46,,,,,DOID:0110409,retinitis pigmentosa 46,C2675496,C567249,612572,MONDO:0012943,retinitis pigmentosa 46,
+BMGC_DS12922,BMG_DS043527,,"INFLAMMATORY BOWEL DISEASE 25, AUTOSOMAL RECESSIVE",,,,,DOID:0110909,inflammatory bowel disease 25,C2675508,,612567,MONDO:0012941,inflammatory bowel disease 25,
+BMGC_DS12923,BMG_DS043528,,Inflammatory Bowel Disease 24,,,,,DOID:0110908,inflammatory bowel disease 24,C2675509,C567252,612566,MONDO:0012940,inflammatory bowel disease 24,
+BMGC_DS12924,BMG_DS043529,,Diamond-Blackfan Anemia 8,,,,,DOID:0111881,Diamond-Blackfan anemia 8,C2675511,C567253,612563,MONDO:0012939,Diamond-Blackfan anemia 8,
+BMGC_DS12925,BMG_DS043530,,Diamond-Blackfan Anemia 7,,,,,DOID:0111878,Diamond-Blackfan anemia 7,C2675512,C567254,612562,MONDO:0012938,Diamond-Blackfan anemia 7,
+BMGC_DS12926,BMG_DS043534,,Adiponectin Deficiency,,,,,,,C2675518,C567258,,,,
+BMGC_DS12927,BMG_DS043535,,Hypoadiponectinemia,,,,,,,C2675519,C567258,,,,
+BMGC_DS12928,BMG_DS043536,,,,,,,,,C2675520,,612555,MONDO:0012933,"breast-ovarian cancer, familial, susceptibility to, 2",
+BMGC_DS12929,BMG_DS043539,,,,,,,,,C2675525,,612551,MONDO:0012931,"focal segmental glomerulosclerosis 4, susceptibility to",
+BMGC_DS12930,BMG_DS043540,,"Myopathy, Congenital, Compton-North",,,,,,,C2675527,C567261,612540,MONDO:0012929,Compton-North congenital myopathy,
+BMGC_DS12931,BMG_DS043541,,"Spastic Paraplegia 42, Autosomal Dominant",,,,,,,C2675528,C567262,612539,MONDO:0012928,hereditary spastic paraplegia 42,
+BMGC_DS12932,BMG_DS043542,,,,,,,,,C2675551,,,MONDO:0100206,"lumbar disk degeneration, susceptibility to",
+BMGC_DS12933,BMG_DS043543,,"Retinitis Pigmentosa 7, Digenic",,,,,,,C2675552,C567263,,,,
+BMGC_DS12934,BMG_DS043545,,,,,,,,,C2675556,,608033,MONDO:0011953,familial acute necrotizing encephalopathy,
+BMGC_DS12935,BMG_DS043547,,,,,,,,,C2675609,,607850,MONDO:0011923,osteoarthritis susceptibility 3,
+BMGC_DS12936,BMG_DS043549,,"Niemann-Pick Disease, Intermediate, Protracted Neurovisceral",,,,,,,C2675646,C567268,,,,
+BMGC_DS12937,BMG_DS043552,,Dyschromatosis Universalis Hereditaria 1,,,,,,,C2675711,C567273,127500,MONDO:0024524,dyschromatosis universalis hereditaria 1,
+BMGC_DS12938,BMG_DS043553,,"Deafness, Congenital, and Onychodystrophy, Autosomal Dominant",,,,,,,C2675730,C567274,124480,MONDO:0007420,autosomal dominant deafness - onychodystrophy syndrome,
+BMGC_DS12939,BMG_DS043554,,"Craniodiaphyseal Dysplasia, Autosomal Dominant",,,,,,,C2675746,C567275,122860,MONDO:0021021,"craniodiaphyseal dysplasia, autosomal dominant",
+BMGC_DS12940,BMG_DS043555,,"Deafness, Autosomal Dominant 3A",,,,,,,C2675750,C567277,601544,MONDO:0011103,autosomal dominant nonsyndromic hearing loss 3A,
+BMGC_DS12941,BMG_DS043556,,"EPIPHYSEAL DYSPLASIA, MULTIPLE, 6",,,,,DOID:0070301,multiple epiphyseal dysplasia 6,C2675767,,120210;614135,MONDO:0013591,"epiphyseal dysplasia, multiple, 6",
+BMGC_DS12942,BMG_DS043558,,Holoprosencephaly 10,,,,,,,C2675857,C567278,612530,MONDO:0012927,chromosome 1q41-q42 deletion syndrome,
+BMGC_DS12943,BMG_DS043559,,"Amelogenesis Imperfecta, Hypomaturation Type, Iia2",,,,,,,C2675858,C567279,612529,MONDO:0012926,amelogenesis imperfecta hypomaturation type 2A2,
+BMGC_DS12944,BMG_DS043560,,Diamond-Blackfan Anemia 5,,,,,DOID:0111883,Diamond-Blackfan anemia 5,C2675859,C567280,612528,MONDO:0012925,Diamond-Blackfan anemia 5,
+BMGC_DS12945,BMG_DS043561,,Diamond-Blackfan Anemia 4,,,,,DOID:0111890,Diamond-Blackfan anemia 4,C2675860,C567281,612527,MONDO:0012924,Diamond-Blackfan anemia 4,
+BMGC_DS12946,BMG_DS043562,,"Lipodystrophy, Congenital Generalized, Type 3",,,,,,,C2675861,C567282,612526,MONDO:0012923,congenital generalized lipodystrophy type 3,
+BMGC_DS12947,BMG_DS043563,,"Pyloric Stenosis, Infantile Hypertrophic, 5",,,,,,,C2675862,C567283,612525,MONDO:0012922,"pyloric stenosis, infantile hypertrophic, 5",
+BMGC_DS12948,BMG_DS043564,,"Diabetes Mellitus, Insulin-Dependent, 22",,,,,,,C2675864,C567284,612522,MONDO:0012921,type 1 diabetes mellitus 22,
+BMGC_DS12949,BMG_DS043566,,"Diabetes Mellitus, Insulin-Dependent, 20",,,,,,,C2675866,C567286,612520,MONDO:0012919,type 1 diabetes mellitus 20,
+BMGC_DS12950,BMG_DS043567,,"CILIARY DYSKINESIA, PRIMARY, 10",,,,,,,C2675867,,612518,MONDO:0012918,primary ciliary dyskinesia 10,
+BMGC_DS12951,BMG_DS043568,,Specific Language Impairment 4,,,,,,,C2675874,C567288,612514,MONDO:0012917,specific language impairment 4,
+BMGC_DS12952,BMG_DS043569,,Chromosome 2p16.1-P15 Deletion Syndrome,,,,,DOID:0060415,chromosome 2p16.1-p15 deletion syndrome,C2675875,C567289,612513,MONDO:0012916,chromosome 2p16.1-p15 deletion syndrome,
+BMGC_DS12953,BMG_DS043570,,Chromosome 1q21.1 Duplication Syndrome,,,,,DOID:0060435,chromosome 1q21.1 duplication syndrome,C2675891,C567290,612475,MONDO:0012915,chromosome 1q21.1 duplication syndrome,
+BMGC_DS12954,BMG_DS043571,,,,,,,,,C2675897,,612474,MONDO:0012914,chromosome 1q21.1 deletion syndrome,
+BMGC_DS12955,BMG_DS043572,,"Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome",,,,,,,C2675904,C567292,612469,MONDO:0012913,"Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome",
+BMGC_DS12956,BMG_DS043573,,,,,,,,,C2675945,,,MONDO:0100182,"schizophrenia, susceptibility to",
+BMGC_DS12957,BMG_DS043576,,"Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant",,,,,,,C2676023,C567296,115300,MONDO:0007272,hereditary hypercarotenemia and vitamin A deficiency,
+BMGC_DS12958,BMG_DS043579,,Diamond-Blackfan Anemia 1,,,,,DOID:0111895,Diamond-Blackfan anemia 1,C2676137,C567302,105650,MONDO:0007110,Diamond-Blackfan anemia 1,
+BMGC_DS12959,BMG_DS043581,,,,,,,,,C2676191,,,MONDO:0017824,familial isolated pituitary adenoma,
+BMGC_DS12960,BMG_DS043584,,"Skeletal Defects, Genital Hypoplasia, And Mental Retardation",,,,,,,C2676231,C567306,612447,MONDO:0012909,"skeletal defects, genital hypoplasia, and intellectual disability",
+BMGC_DS12961,BMG_DS043585,,Complement Component 6 Deficiency,,,,,DOID:0060299,complement component 6 deficiency,C2676232,C567307,612446,MONDO:0012908,complement component 6 deficiency,
+BMGC_DS12962,BMG_DS043588,,"CILIARY DYSKINESIA, PRIMARY, 9",,,,,,,C2676235,,612444,MONDO:0012906,primary ciliary dyskinesia 9,
+BMGC_DS12963,BMG_DS043589,,"Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism",,,,,,,C2676243,C567313,607694,MONDO:0011897,leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome,
+BMGC_DS12964,BMG_DS043590,,"Leukodystrophy, Hypomyelinating, 6",,,,,,,C2676244,C567314,612438,MONDO:0012905,hypomyelinating leukodystrophy 6,
+BMGC_DS12965,BMG_DS043591,,Prickle1-Related Progressive Myoclonus Epilepsy with Ataxia,,,,,,,C2676254,C580388,612437,MONDO:0012904,"epilepsy, progressive myoclonic, 1B",
+BMGC_DS12966,BMG_DS043592,,"Cardiomyopathy, Familial Restrictive, 3",,,,,,,C2676271,C567316,612422,MONDO:0012900,"cardiomyopathy, familial restrictive, 3",
+BMGC_DS12967,BMG_DS043595,,"Dystonia 17, Torsion, Autosomal Recessive",,,,,,,C2676281,C567319,612406,MONDO:0012895,torsion dystonia 17,
+BMGC_DS12968,BMG_DS043596,,"Bone Fragility with Contractures, Arterial Rupture, and Deafness",,,,,,,C2676285,C567320,612394,MONDO:0012892,"bone fragility with contractures, arterial rupture, and deafness",
+BMGC_DS12969,BMG_DS043597,,Pontocerebellar Hypoplasia Type 2C,,,,,DOID:0060269,pontocerebellar hypoplasia type 2C,C2676465,C567324,612390,MONDO:0012891,pontocerebellar hypoplasia type 2C,
+BMGC_DS12970,BMG_DS043598,,Pontocerebellar Hypoplasia Type 2B,,,,,DOID:0060268,pontocerebellar hypoplasia type 2B,C2676466,C567325,612389,MONDO:0012890,pontocerebellar hypoplasia type 2B,
+BMGC_DS12971,BMG_DS043600,,,,,,,,,C2676468,,612387,MONDO:0012888,"sarcoidosis, susceptibility to, 2",
+BMGC_DS12972,BMG_DS043601,,Inflammatory Bowel Disease 23,,,,,DOID:0110884,inflammatory bowel disease 23,C2676484,C567326,612381,MONDO:0012887,inflammatory bowel disease 23,
+BMGC_DS12973,BMG_DS043602,,Inflammatory Bowel Disease 22,,,,,DOID:0110905,inflammatory bowel disease 22,C2676485,C567327,612380,MONDO:0012886,inflammatory bowel disease 22,
+BMGC_DS12974,BMG_DS043604,,Cowden-Like Syndrome,,,,,,,C2676500,C567337,612359,MONDO:0012878,Cowden syndrome 2,
+BMGC_DS12975,BMG_DS043605,,Inflammatory Bowel Disease 21,,,,,DOID:0110906,inflammatory bowel disease 21,C2676507,C567338,612354,MONDO:0012875,inflammatory bowel disease 21,
+BMGC_DS12976,BMG_DS043606,,"Porokeratosis, Disseminated Superficial Actinic, 4",,,,,,,C2676508,C567339,612353,MONDO:0012874,"porokeratosis 6, disseminated superficial actinic type",
+BMGC_DS12977,BMG_DS043607,,"Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like",,,,,,,C2676510,C567340,612350,MONDO:0012873,"Ehlers-Danlos syndrome, spondylocheirodysplastic type",
+BMGC_DS12978,BMG_DS043608,,,,,,,,,C2676676,,604370,MONDO:0011450,"breast-ovarian cancer, familial, susceptibility to, 1",
+BMGC_DS12979,BMG_DS043610,,"Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator",,,,,DOID:0111906,thrombophilia due to decreased release of PLAT,C2676721,C567341,612348,MONDO:0012872,"thrombophilia, familial, due to decreased release of tissue plasminogen activator",
+BMGC_DS12980,BMG_DS043612,,Jervell And Lange-Nielsen Syndrome 2,,,,,,,C2676723,C567343,612347,MONDO:0012871,Jervell and Lange-Nielsen syndrome 2,
+BMGC_DS12981,BMG_DS043614,,Chromosome 1q43-Q44 Deletion Syndrome,,,,,,,C2676727,C567346,612337,MONDO:0012869,"intellectual disability, autosomal dominant 22",
+BMGC_DS12982,BMG_DS043615,,"Spastic Paraplegia 38, Autosomal Dominant",,,,,,,C2676732,C567349,612335,MONDO:0012867,hereditary spastic paraplegia 38,
+BMGC_DS12983,BMG_DS043616,,Chromosome 2q32-Q33 Deletion Syndrome,,,,,DOID:0060428,SATB2-associated syndrome,C2676739,C567350,612313,MONDO:0012864,chromosome 2q32-q33 deletion syndrome,
+BMGC_DS12984,BMG_DS043619,,Premature Ovarian Failure 6,,,,,,,C2676742,C567351,612310,MONDO:0012861,premature ovarian failure 6,
+BMGC_DS12985,BMG_DS043620,,"THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE",,,,,DOID:0111904,autosomal recessive thrombophilia due to protein C deficiency,C2676759,,612283;612304,MONDO:0012860,"thrombophilia due to protein C deficiency, autosomal recessive",
+BMGC_DS12986,BMG_DS043621,,"Osteopetrosis, Autosomal Recessive 7",,,,,,,C2676766,C567354,612301,MONDO:0012859,autosomal recessive osteopetrosis 7,
+BMGC_DS12987,BMG_DS043622,,CD59 Deficiency,,,,,,,C2676767,C567355,612300,MONDO:0012858,primary CD59 deficiency,
+BMGC_DS12988,BMG_DS043624,,Birk-Barel Mental Retardation Dysmorphism Syndrome,,,,,DOID:0050675,Birk-Barel syndrome,C2676770,C567357,612292,MONDO:0012856,Birk-Barel syndrome,
+BMGC_DS12989,BMG_DS043625,,Joubert Syndrome 8,,,,,DOID:0111003,Joubert syndrome 8,C2676771,C567358,612291,MONDO:0012855,Joubert syndrome 8,
+BMGC_DS12990,BMG_DS043626,,"Microtia, Hearing Impairment, And Cleft Palate",,,,,,,C2676772,C567359,612290,MONDO:0012854,bilateral microtia-deafness-cleft palate syndrome,
+BMGC_DS12991,BMG_DS043627,,FONTAINE PROGEROID SYNDROME,,,,,,,C2676780,,608744;612289;233500;612289,MONDO:0012853,Fontaine progeroid syndrome,
+BMGC_DS12992,BMG_DS043628,,Inflammatory Bowel Disease 20,,,,,DOID:0110898,inflammatory bowel disease 20,C2676781,C567361,612288,MONDO:0012852,inflammatory bowel disease 20,
+BMGC_DS12993,BMG_DS043629,,"Nephrolithiasis-Osteoporosis, Hypophosphatemic, 2",,,,,DOID:0080078,hypophosphatemic nephrolithiasis/osteoporosis 2,C2676782,C567362,612287,MONDO:0012851,hypophosphatemic nephrolithiasis/osteoporosis 2,
+BMGC_DS12994,BMG_DS043630,,"Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1",,,,,DOID:0080077,hypophosphatemic nephrolithiasis/osteoporosis 1,C2676786,C567363,612286,MONDO:0012850,hypophosphatemic nephrolithiasis/osteoporosis 1,
+BMGC_DS12995,BMG_DS043631,,Joubert Syndrome 9,,,,,DOID:0111004,Joubert syndrome 9,C2676788,C567364,612285,MONDO:0012849,Joubert syndrome 9,
+BMGC_DS12996,BMG_DS043632,,"Meckel Syndrome, Type 6",,,,,,,C2676790,C567365,612284,MONDO:0012848,"Meckel syndrome, type 6",
+BMGC_DS12997,BMG_DS043633,,,,,,,,,C2676832,,603933,MONDO:0011386,"microvascular complications of diabetes, susceptibility to, 1",
+BMGC_DS12998,BMG_DS043634,,,,,,,,,C2676840,,,MONDO:0100202,"lumbar disk herniation, susceptibility to",
+BMGC_DS12999,BMG_DS043635,,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6",,,,,,,C2677065,,609383;612281,MONDO:0012847,autosomal recessive congenital ichthyosis 6,
+BMGC_DS13000,BMG_DS043637,,Inflammatory Bowel Disease 19,,,,,DOID:0110890,inflammatory bowel disease 19,C2677079,C567372,612278,MONDO:0012845,inflammatory bowel disease 19,
+BMGC_DS13001,BMG_DS043639,,,,,,,,,C2677087,,612269,MONDO:0012843,"epilepsy, childhood absence, susceptibility to, 5",
+BMGC_DS13002,BMG_DS043641,,Inflammatory Bowel Disease 18,,,,,DOID:0110888,inflammatory bowel disease 18,C2677090,C567377,612262,MONDO:0012841,inflammatory bowel disease 18,
+BMGC_DS13003,BMG_DS043642,,Inflammatory Bowel Disease 17,,,,,DOID:0110883,inflammatory bowel disease 17,C2677091,C567378,612261,MONDO:0012840,inflammatory bowel disease 17,
+BMGC_DS13004,BMG_DS043643,,MYD88 Deficiency,,,,,,,C2677092,C567379,612260,MONDO:0012839,pyogenic bacterial infections due to MyD88 deficiency,
+BMGC_DS13005,BMG_DS043644,,Inflammatory Bowel Disease 16,,,,,DOID:0110896,inflammatory bowel disease 16,C2677093,C567380,612259,MONDO:0012838,inflammatory bowel disease 16,
+BMGC_DS13006,BMG_DS043645,,Inflammatory Bowel Disease 15,,,,,DOID:0110897,inflammatory bowel disease 15,C2677094,C567381,612255,MONDO:0012837,inflammatory bowel disease 15,
+BMGC_DS13007,BMG_DS043647,,,,,,,,,C2677096,,612253,MONDO:0012835,"systemic lupus erythematosus, susceptibility to, 11",
+BMGC_DS13008,BMG_DS043648,,,,,,,,,C2677097,,612251,MONDO:0012834,"systemic lupus erythematosus, susceptibility to, 10",
+BMGC_DS13009,BMG_DS043649,,,,,,,,,C2677099,,612247,MONDO:0012833,Crouzon syndrome-acanthosis nigricans syndrome,
+BMGC_DS13010,BMG_DS043650,,Inflammatory Bowel Disease 14,,,,,DOID:0110895,inflammatory bowel disease 14,C2677100,C567383,612245,MONDO:0012832,inflammatory bowel disease 14,
+BMGC_DS13011,BMG_DS043651,,Inflammatory Bowel Disease 13,,,,,DOID:0110893,inflammatory bowel disease 13,C2677101,C567384,612244,MONDO:0012831,inflammatory bowel disease 13,
+BMGC_DS13012,BMG_DS043653,,Inflammatory Bowel Disease 12,,,,,DOID:0110887,inflammatory bowel disease 12,C2677105,C567388,612241,MONDO:0012829,inflammatory bowel disease 12,
+BMGC_DS13013,BMG_DS043654,,"Atrial Fibrillation, Familial, 7",,,,,,,C2677106,C567389,612240,MONDO:0012828,"atrial fibrillation, familial, 7",
+BMGC_DS13014,BMG_DS043657,,"Leukodystrophy, Hypomyelinating, 4",,,,,,,C2677109,C567390,612233,MONDO:0012824,hypomyelinating leukodystrophy 4,
+BMGC_DS13015,BMG_DS043658,,"Leukodystrophy, hypomyelinating",,,,,,,C2677112,,MTHU021394,,,
+BMGC_DS13016,BMG_DS043662,,,,,,,,,C2677123,,612229,MONDO:0012820,"colorectal cancer, susceptibility to, 3",
+BMGC_DS13017,BMG_DS043664,,,,,,,,,C2677132,,612225,MONDO:0012818,maturity-onset diabetes of the young type 9,
+BMGC_DS13018,BMG_DS043665,,"Lymphedema, Cardiac Septal Defects, And Characteristic Facies",,,,,,,C2677167,C567398,601927,MONDO:0011166,lymphedema-atrial septal defects-facial changes syndrome,
+BMGC_DS13019,BMG_DS043668,,"Atrial Fibrillation, Familial, 6",,,,,,,C2677294,C567400,612201,MONDO:0012816,"atrial fibrillation, familial, 6",
+BMGC_DS13020,BMG_DS043669,,,,,,,,,C2677299,,,MONDO:0012815,Coats plus syndrome,
+BMGC_DS13021,BMG_DS043670,,Diastasis Recti And Weakness Of The Linea Alba,,,,,,,C2677303,C567402,612198,MONDO:0012814,diastasis recti and weakness of the linea alba,
+BMGC_DS13022,BMG_DS043671,,Retinitis Pigmentosa 29,,,,,DOID:0110378,retinitis pigmentosa 29,C2677325,C567403,612165,MONDO:0012813,retinitis pigmentosa 29,
+BMGC_DS13023,BMG_DS043672,,"Epileptic Encephalopathy, Early Infantile, 4",,,,,,,C2677326,C567404,612164,MONDO:0012812,"developmental and epileptic encephalopathy, 4",
+BMGC_DS13024,BMG_DS043675,,"Cardiomyopathy, Dilated, 1AA",,,,,,,C2677338,C567407,612158,MONDO:0012808,dilated cardiomyopathy 1AA,
+BMGC_DS13025,BMG_DS043676,,Epidermolysis Bullosa Simplex With Pyloric Atresia,,,,,,,C2677349,C567408,612138,MONDO:0012807,"epidermolysis bullosa simplex 5C, with pyloric atresia",
+BMGC_DS13026,BMG_DS043677,,OROFACIAL CLEFT 11,,,,,,,C2677434,,112262;600625,MONDO:0010906,orofacial cleft 11,
+BMGC_DS13027,BMG_DS043678,,"Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant",,,,,,,C2677481,C567411,612132,MONDO:0012806,ectodermal dysplasia and immunodeficiency 2,
+BMGC_DS13028,BMG_DS043679,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12",,,,,DOID:0110318,hypertrophic cardiomyopathy 12,C2677491,,600824;612124,MONDO:0012804,hypertrophic cardiomyopathy 12,
+BMGC_DS13029,BMG_DS043680,,Oculoauricular Syndrome,,,,,DOID:0060482,oculoauricular syndrome,C2677500,C567416,612109,MONDO:0012802,oculoauricular syndrome,
+BMGC_DS13030,BMG_DS043681,,,,,,,,,C2677504,,612100,MONDO:0012801,"autism, susceptibility to, 15",
+BMGC_DS13031,BMG_DS043682,,"Trichoepithelioma, Multiple Familial, 2",,,,,,,C2677505,C567418,612099,MONDO:0012800,"trichoepithelioma, multiple familial, 2",
+BMGC_DS13032,BMG_DS043683,,"Cardiomyopathy, Familial Hypertrophic, 11",,,,,,,C2677506,C567419,612098,MONDO:0012799,hypertrophic cardiomyopathy 11,
+BMGC_DS13033,BMG_DS043684,,"Deafness, Unilateral, With Delayed Endolymphatic Hydrops",,,,,,,C2677512,C567420,612097,MONDO:0012798,"deafness, unilateral, with delayed endolymphatic hydrops",
+BMGC_DS13034,BMG_DS043685,,Otosclerosis 8,,,,,,,C2677515,C567421,612096,MONDO:0012797,otosclerosis 8,
+BMGC_DS13035,BMG_DS043686,,Retinitis Pigmentosa 41,,,,,DOID:0110376,retinitis pigmentosa 41,C2677516,C567422,612095,MONDO:0012796,retinitis pigmentosa 41,
+BMGC_DS13036,BMG_DS043687,,Hypophosphatemic Rickets And Hyperparathyroidism,,,,,,,C2677524,C567423,612089,MONDO:0012795,hypophosphatemic rickets and hyperparathyroidism,
+BMGC_DS13037,BMG_DS043688,,"Alopecia, Neurologic Defects, and Endocrinopathy Syndrome",,,,,DOID:0112244,"alopecia, neurologic defects, and endocrinopathy syndrome",C2677535,C567425,612079,MONDO:0012794,ANE syndrome,
+BMGC_DS13038,BMG_DS043689,,"Hypouricemia, Renal, 2",,,,,,,C2677549,C567426,612076,MONDO:0012793,"hypouricemia, renal, 2",
+BMGC_DS13039,BMG_DS043690,,Amyotrophic Lateral Sclerosis 10,,,,,,,C2677565,C567429,612069,MONDO:0012790,amyotrophic lateral sclerosis type 10,
+BMGC_DS13040,BMG_DS043691,,,,,,,,,C2677567,,612067,MONDO:0012789,dystonia 16,
+BMGC_DS13041,BMG_DS043693,,"Spastic Paraplegia 39, Autosomal Recessive",,,,,,,C2677586,C567433,612020,MONDO:0012787,hereditary spastic paraplegia 39,
+BMGC_DS13042,BMG_DS043694,,"Cataract, Juvenile, With Microcornea And Glucosuria",,,,,,,C2677587,C567434,,,,
+BMGC_DS13043,BMG_DS043696,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9",,,,,DOID:0070241,primary coenzyme Q10 deficiency 4,C2677589,,612016,MONDO:0012784,autosomal recessive ataxia due to ubiquinone deficiency,
+BMGC_DS13044,BMG_DS043697,,"Congenital Disorder Of Glycosylation, Type In",,,,,,,C2677590,C567437,612015,MONDO:0012783,RFT1-congenital disorder of glycosylation,
+BMGC_DS13045,BMG_DS043698,,,,,,,,,C2677601,,612011,MONDO:0012782,"celiac disease, susceptibility to, 13",
+BMGC_DS13046,BMG_DS043705,,Thrombocytopenia 4,,,,,,,C2677608,C567438,612004,MONDO:0012775,thrombocytopenia 4,
+BMGC_DS13047,BMG_DS043706,,Chromosome 15q13.3 Microdeletion Syndrome,,,,,DOID:0060394,chromosome 15q13.3 microdeletion syndrome,C2677613,C567439,612001,MONDO:0012774,chromosome 15q13.3 microdeletion syndrome,
+BMGC_DS13048,BMG_DS043707,,SCHIZOPHRENIA 14,,,,,DOID:0070090,schizophrenia 14,C2677614,,612361,MONDO:0012879,schizophrenia 14,
+BMGC_DS13049,BMG_DS043708,,"Deafness, Autosomal Dominant 2A",,,,,,,C2677637,C567441,600101,MONDO:0010817,autosomal dominant nonsyndromic hearing loss 2A,
+BMGC_DS13050,BMG_DS043709,,"Rett Syndrome, Zappella Variant",,,,,,,C2677682,C567442,,,,
+BMGC_DS13051,BMG_DS043711,,Hunter-Macdonald Syndrome,,,,,,,C2677745,C567445,611962,MONDO:0012773,Hunter-Macdonald syndrome,
+BMGC_DS13052,BMG_DS043712,,Stevenson-Carey Syndrome,,,,,,,C2677763,C567446,611961,MONDO:0012772,Stevenson-Carey syndrome,
+BMGC_DS13053,BMG_DS043713,,,,,,,,,C2677770,,611960,MONDO:0012771,"asthma-related traits, susceptibility to, 7",
+BMGC_DS13054,BMG_DS043717,,"Macular Degeneration, Age-Related, 11",,,,,,,C2677774,C567450,611953,MONDO:0012767,age related macular degeneration 11,
+BMGC_DS13055,BMG_DS043720,,Riddle Syndrome,,,,,DOID:0090113,RIDDLE syndrome,C2677792,C567453,611943,MONDO:0012764,RIDDLE syndrome,
+BMGC_DS13056,BMG_DS043721,,,,,,,,,C2677793,,,MONDO:0800279,"epilepsy, idiopathic generalized, susceptibility to, 6",
+BMGC_DS13057,BMG_DS043722,,,,,,,,,C2677794,,611938,MONDO:0012762,catecholaminergic polymorphic ventricular tachycardia 2,
+BMGC_DS13058,BMG_DS043724,,"Camptodactyly Syndrome, Guadalajara, Type III",,,,,,,C2677809,C567455,611929,MONDO:0012759,"camptodactyly syndrome, Guadalajara type 3",
+BMGC_DS13059,BMG_DS043725,,,,,,,,,C2677821,,611928,MONDO:0012758,"prostate cancer, hereditary, 13",
+BMGC_DS13060,BMG_DS043726,,"Episodic Ataxia, Type 7",,,,,,,C2677843,C567459,611907,MONDO:0012755,episodic ataxia type 7,
+BMGC_DS13061,BMG_DS043727,,"Surfactant Metabolism Dysfunction, Pulmonary, 4",,,,,,,C2677877,C567461,300770,MONDO:0010424,"surfactant metabolism dysfunction, pulmonary, 4",
+BMGC_DS13062,BMG_DS043728,,"Hypospadias 2, X-Linked",,,,,,,C2677879,C567462,300758,MONDO:0010423,"hypospadias 2, X-linked",
+BMGC_DS13063,BMG_DS043730,,"Protoporphyria, Erythropoietic, X-Linked Dominant",,,,,,,C2677889,C567464,300752,MONDO:0010420,X-linked erythropoietic protoporphyria,
+BMGC_DS13064,BMG_DS043731,,"Spastic Paraplegia 34, X-Linked",,,,,,,C2677897,C567465,300750,MONDO:0010418,hereditary spastic paraplegia 34,
+BMGC_DS13065,BMG_DS043732,,Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia,,,,,,,C2677903,C567466,300749,MONDO:0010417,syndromic X-linked intellectual disability Najm type,
+BMGC_DS13066,BMG_DS043733,,"Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities",,,,,,,C2678011,C567467,300719,MONDO:0010416,"deafness, cataract, retinitis pigmentosa, and sperm abnormalities",
+BMGC_DS13067,BMG_DS043734,,"Myopathy, Reducing Body, X-Linked, Childhood-Onset",,,,,,,C2678015,C567468,,,,
+BMGC_DS13068,BMG_DS043735,,"Myopathy, Reducing Body, X-Linked, Early-Onset, Severe",,,,,,,C2678027,C567469,,,,
+BMGC_DS13069,BMG_DS043736,,,,,,,,,C2678034,,300716,MONDO:0010413,"intellectual disability, X-linked 95",
+BMGC_DS13070,BMG_DS043737,,Craniofacioskeletal Syndrome,,,,,,,C2678036,C567471,300712,MONDO:0010412,X-linked intellectual disability-craniofacioskeletal syndrome,
+BMGC_DS13071,BMG_DS043740,,,,,,,,,C2678039,,300709,MONDO:0010409,syndromic X-linked intellectual disability Shrimpton type,
+BMGC_DS13072,BMG_DS043741,,"TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS",,,,,DOID:0111931,syndactyly-telecanthus-anogenital and renal malformations syndrome,C2678045,,300707,MONDO:0010408,syndactyly-telecanthus-anogenital and renal malformations syndrome,
+BMGC_DS13073,BMG_DS043742,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE",,,,,,,C2678046,,300697;300612;300706;309590;309590,MONDO:0010407,"intellectual disability, X-linked syndromic, Turner type",
+BMGC_DS13074,BMG_DS043744,,"Spinocerebellar Ataxia, X-Linked 5",,,,,DOID:0111833,X-linked spinocerebellar ataxia 5,C2678048,C567478,300703,MONDO:0010404,X-linked non progressive cerebellar ataxia,
+BMGC_DS13075,BMG_DS043745,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, WU TYPE",,,,,,,C2678051,,300699,MONDO:0010402,syndromic X-linked intellectual disability 94,
+BMGC_DS13076,BMG_DS043746,,"Myopathy, X-Linked, With Postural Muscle Atrophy",X-Linked Emery-Dreifuss Muscular Dystrophy,,,,,,C2678055,D000083143,300696,MONDO:0010401,X-linked myopathy with postural muscle atrophy,
+BMGC_DS13077,BMG_DS043747,,"SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT",,,,,,,C2678061,,300163;300695,MONDO:0010400,X-linked scapuloperoneal muscular dystrophy,
+BMGC_DS13078,BMG_DS043748,,Myofibrillar Myopathy,,,,,DOID:0080307,myofibrillar myopathy,C2678065,C580316,,MONDO:0018943,myofibrillar myopathy,
+BMGC_DS13079,BMG_DS043749,,"Hypospadias 1, X-Linked",,,,,,,C2678098,C567482,300633,MONDO:0010384,"hypospadias 1, X-linked",
+BMGC_DS13080,BMG_DS043750,,Periventricular Laminar Heterotopia,,,,,,,C2678104,C548481,,,,
+BMGC_DS13081,BMG_DS043753,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE",,,,,,,C2678194,,300231;300243,MONDO:0010278,Christianson syndrome,
+BMGC_DS13082,BMG_DS043754,,"Mental Retardation, X-Linked, With Panhypopituitarism",,,,,,,C2678223,C567485,300123,MONDO:0010252,"intellectual disability, X-linked, with panhypopituitarism",
+BMGC_DS13083,BMG_DS043756,,"Hypercarotenemia And Vitamin A Deficiency, Autosomal Recessive",,,,,,,C2678266,C567486,277350,MONDO:0010182,"hypercarotenemia and vitamin A deficiency, autosomal recessive",
+BMGC_DS13084,BMG_DS043757,,Thrombocytopenia 3,,,,,,,C2678311,C567487,273900,MONDO:0010120,thrombocytopenia 3,
+BMGC_DS13085,BMG_DS043758,,Three M Syndrome 1,,,,,,,C2678312,C535314,273750,MONDO:0010117,3M syndrome 1,
+BMGC_DS13086,BMG_DS043759,,"Spherocytosis, Type 3",,,,,,,C2678338,C567489,270970,MONDO:0010053,hereditary spherocytosis type 3,
+BMGC_DS13087,BMG_DS043761,,,,,,,,,C2678403,,,MONDO:0800410,"UV-induced skin damage, susceptibility to",
+BMGC_DS13088,BMG_DS043762,,"PITUITARY HORMONE DEFICIENCY, COMBINED, 4",,,,,DOID:0061017,combined pituitary hormone deficiency 4,C2678408,,262700;602146,MONDO:0009880,short stature-pituitary and cerebellar defects-small sella turcica syndrome,
+BMGC_DS13089,BMG_DS043764,,"Hyperphenylalaninemia, Non-Pku Mild",,,,,,,C2678416,C567494,,,,
+BMGC_DS13090,BMG_DS043765,,CRANIOOSTEOARTHROPATHY,,,,,,,C2678439,,259100;601688,MONDO:0015466,cranio-osteoarthropathy,
+BMGC_DS13091,BMG_DS043766,,Nanophthalmos 3,,,,,,,C2678467,C567498,611897,MONDO:0012754,nanophthalmos 3,
+BMGC_DS13092,BMG_DS043767,,Amyotrophic Lateral Sclerosis 9,,,,,,,C2678468,C567499,611895,MONDO:0012753,amyotrophic lateral sclerosis type 9,
+BMGC_DS13093,BMG_DS043770,,Lethal Arthrogryposis With Anterior Horn Cell Disease,,,,,,,C2678471,C567502,,,,
+BMGC_DS13094,BMG_DS043772,,"Ciliary Dyskinesia, Primary, 7",,,,,,,C2678473,C567504,611884,MONDO:0012748,primary ciliary dyskinesia 7,
+BMGC_DS13095,BMG_DS043773,,"Cardiomyopathy, Dilated, 2a",,,,,,,C2678474,C567505,611880,MONDO:0012746,dilated cardiomyopathy 2A,
+BMGC_DS13096,BMG_DS043774,,"Cardiomyopathy, Dilated, 1z",,,,,,,C2678475,C567506,611879,MONDO:0012745,dilated cardiomyopathy 1Z,
+BMGC_DS13097,BMG_DS043775,,"Cardiomyopathy, Dilated, 1y",,,,,,,C2678476,C567507,611878,MONDO:0012744,dilated cardiomyopathy 1Y,
+BMGC_DS13098,BMG_DS043776,,Brugada Syndrome 4,,,,,DOID:0110221,Brugada syndrome 4,C2678477,C567508,611876,MONDO:0012743,Brugada syndrome 4,
+BMGC_DS13099,BMG_DS043777,,Brugada Syndrome 3,,,,,DOID:0110220,Brugada syndrome 3,C2678478,C567509,611875,MONDO:0012742,Brugada syndrome 3,
+BMGC_DS13100,BMG_DS043778,,,,,,,,,C2678479,,611868,MONDO:0012741,"prostate cancer, hereditary, 12",
+BMGC_DS13101,BMG_DS043779,,"Chromosome 22q11.2 Deletion Syndrome, Distal",,,,,DOID:0060413,"chromosome 22q11.2 deletion syndrome, distal",C2678480,C567511,611867,MONDO:0012740,"chromosome 22q11.2 deletion syndrome, distal",
+BMGC_DS13102,BMG_DS043780,,Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma,,,,,,,C2678482,C567512,611863,MONDO:0012739,microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome,
+BMGC_DS13103,BMG_DS043781,,Long Qt Syndrome 11,,,,,DOID:0110652,long QT syndrome 11,C2678483,C567513,611820,MONDO:0012738,long QT syndrome 11,
+BMGC_DS13104,BMG_DS043782,,Long Qt Syndrome 10,,,,,DOID:0110651,long QT syndrome 10,C2678484,C567514,611819,MONDO:0012737,long QT syndrome 10,
+BMGC_DS13105,BMG_DS043783,,Long Qt Syndrome 9,,,,,DOID:0110650,long QT syndrome 9,C2678485,C567515,611818,MONDO:0012736,long QT syndrome 9,
+BMGC_DS13106,BMG_DS043784,,Temple-Baraitser Syndrome,,,,,,,C2678486,C567516,611816,MONDO:0012735,Temple-Baraitser syndrome,
+BMGC_DS13107,BMG_DS043785,,"Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs",,,,,,,C2678492,C567517,611812,MONDO:0012734,SERKAL syndrome,
+BMGC_DS13108,BMG_DS043786,,"Tremor, Hereditary Essential, And Idiopathic Normal Pressure Hydrocephalus",,,,,,,C2678494,C567519,611808,MONDO:0012732,"tremor, hereditary essential, and idiopathic normal pressure hydrocephalus",
+BMGC_DS13109,BMG_DS043787,,Elliptocytosis 1,,,,,,,C2678497,C567520,611804,MONDO:0012731,elliptocytosis 1,
+BMGC_DS13110,BMG_DS043788,,"AXENFELD-RIEGER SYNDROME, TYPE 3",,,,,,,C2678503,,601090;602482,MONDO:0011233,Axenfeld-Rieger syndrome type 3,
+BMGC_DS13111,BMG_DS043789,,"SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE",,,,,,,C2680446,,614297;615043,MONDO:0014024,hereditary spastic paraplegia 43,
+BMGC_DS13112,BMG_DS043790,,"HYPERPIGMENTATION, FAMILIAL PROGRESSIVE, 1",,,,,,,C2681535,,614233,,,
+BMGC_DS13113,BMG_DS043791,,Retinitis Pigmentosa 2,,,,,DOID:0110415,retinitis pigmentosa 2,C2681923,C567523,312600,MONDO:0010723,retinitis pigmentosa 2,
+BMGC_DS13114,BMG_DS043792,,,,,,,,,C2684859,,,MONDO:0800414,"aplastic anemia, susceptibility to",
+BMGC_DS13115,BMG_DS043793,,,,,,,,,C2697310,,181000,MONDO:0008399,"sarcoidosis, susceptibility to, 1",
+BMGC_DS13116,BMG_DS043794,,,,,,,,,C2697358,,,MONDO:0017968,"46,XY ovotesticular disorder of sex development",
+BMGC_DS13117,BMG_DS043796,,,,,,,,,C2697447,,163100,MONDO:0008096,nevus flammeus of nape of neck,
+BMGC_DS13118,BMG_DS043797,,Loeys-Dietz Syndrome,Loeys-Dietz Syndrome,,,,DOID:0050466,Loeys-Dietz syndrome,C2697932,D055947,,MONDO:0018954,Loeys-Dietz syndrome,
+BMGC_DS13119,BMG_DS043798,,,,,,,DOID:0080646,B-lymphoblastic leukemia/lymphoma with hyperdiploidy,C2698311,,,MONDO:0035943,B-lymphoblastic leukemia/lymphoma with hyperdiploidy,
+BMGC_DS13120,BMG_DS043799,,,,,,,DOID:0080647,B-lymphoblastic leukemia/lymphoma with hypodiploidy,C2698312,,,MONDO:0035944,B-lymphoblastic leukemia/lymphoma with hypodiploidy,
+BMGC_DS13121,BMG_DS043800,,,,,,,,,C2698313,,,MONDO:0035605,B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality,
+BMGC_DS13122,BMG_DS043801,,,,,,,,,C2698315,,,MONDO:0600030,B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1),
+BMGC_DS13123,BMG_DS043805,,,,,,,,,C2699510,,,MONDO:0017449,split hand,
+BMGC_DS13124,BMG_DS043807,,,,,,,DOID:0060242,synpolydactyly,C2699746,,,MONDO:0021651,synpolydactyly,
+BMGC_DS13125,BMG_DS043811,,,,,,,,,C2700265,,,MONDO:0019517,Waardenburg syndrome type 2,
+BMGC_DS13126,BMG_DS043812,,"WAARDENBURG SYNDROME, TYPE IIE",,,,,DOID:0110956,Waardenburg syndrome type 2E,C2700405,,611584,MONDO:0012698,Waardenburg syndrome type 2E,
+BMGC_DS13127,BMG_DS043813,,,,,,,,,C2700406,,181800,MONDO:0008419,"scoliosis, isolated, susceptibility to, 1",
+BMGC_DS13128,BMG_DS043814,,"EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE",,,,,DOID:0080733,Ehlers-Danlos syndrome dermatosparaxis type,C2700425,,225410;604539,MONDO:0009161,"Ehlers-Danlos syndrome, dermatosparaxis type",
+BMGC_DS13129,BMG_DS043815,,,,,,,,,C2700426,,605990,MONDO:0011622,"nephrolithiasis, uric acid, susceptibility to",
+BMGC_DS13130,BMG_DS043816,,,,,,,,,C2700438,,612371,MONDO:0012881,major affective disorder 7,
+BMGC_DS13131,BMG_DS043819,,Omenn Syndrome,Severe Combined Immunodeficiency,,,,,,C2700553,D016511,603554,MONDO:0011338,Omenn syndrome,
+BMGC_DS13132,BMG_DS043842,442438000,Influenza caused by Influenza A virus,,,,,,,C2711180,,,,,Influenza caused by Influenza A virus (disorder) | Influenza caused by Influenza A virus
+BMGC_DS13133,BMG_DS043846,442191002,Steatohepatitis,Fatty Liver,,,,,,C2711227,D005234,,MONDO:0004790,fatty liver disease,Steatohepatitis | Steatohepatitis (disorder)
+BMGC_DS13134,BMG_DS043852,,,,,,,,,C2711248,,,MONDO:0018378,osteonecrosis of the jaw,
+BMGC_DS13135,BMG_DS043853,441575009,Ischemic priapism,,,,,,,C2711256,,,,,Ischaemic priapism | Ischemic priapism | Low flow priapism | Veno-occlusive priapism | Ischemic priapism (disorder)
+BMGC_DS13136,BMG_DS043888,442459007,Combined immunodeficiency disease,,,,,DOID:628,combined T cell and B cell immunodeficiency,C2711630,,,MONDO:0015131,combined immunodeficiency,Combined immunodeficiency disease | Combined immunodeficiency disease (disorder)
+BMGC_DS13137,BMG_DS043890,442481002,Epilepsy characterized by intractable complex partial seizures,,,,,,,C2711653,,,,,Epilepsy characterised by intractable complex partial seizures | Epilepsy characterized by intractable complex partial seizures | Epilepsy characterized by intractable complex partial seizures (disorder)
+BMGC_DS13138,BMG_DS043904,441891001,Lateral cystocele,,,,,DOID:14130,lateral cystocele,C2711750,,,MONDO:0001885,lateral cystocele,Lateral cystocele | Lateral cystocele (disorder)
+BMGC_DS13139,BMG_DS043929,,Gout attack,,,,M10,,,C2712871,,,,,
+BMGC_DS13140,BMG_DS043934,,Arylsulfatase A Deficiency,"Leukodystrophy, Metachromatic",,,,,,C2713319,D007966,,,,
+BMGC_DS13141,BMG_DS043935,,alpha-L-Iduronidase Deficiency,Mucopolysaccharidosis I,,,,,,C2713321,D008059,,,,
+BMGC_DS13142,BMG_DS043936,,7-Dehydrocholesterol Reductase Deficiency,Smith-Lemli-Opitz Syndrome,,,,,,C2713347,D019082,,,,
+BMGC_DS13143,BMG_DS043937,,,,,,,DOID:0050908,myelodysplastic syndrome,C2713368,,,,,
+BMGC_DS13144,BMG_DS043938,,"Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency",Oculocerebrorenal Syndrome,,,,,,C2713392,D009800,,,,
+BMGC_DS13145,BMG_DS043939,,Haim-Monk Syndrome,Papillon-Lefevre Disease,,,,,,C2713394,D010214,,,,
+BMGC_DS13146,BMG_DS043940,,"Polyposis, Adenomatous Intestinal",Adenomatous Polyposis Coli,,,,,,C2713442,D011125,175100,MONDO:0021056,familial adenomatous polyposis 1,
+BMGC_DS13147,BMG_DS043941,,Familial Intestinal Polyposis,Adenomatous Polyposis Coli,,,,,,C2713443,D011125,,,,
+BMGC_DS13148,BMG_DS043942,,"Hyperpotassemia and Hypertension, Familial",Pseudohypoaldosteronism,,,,,,C2713447,D011546,,,,
+BMGC_DS13149,BMG_DS043943,,Total Hexosaminidase Deficiency,Sandhoff Disease,,,,,,C2713499,D012497,,,,
+BMGC_DS13150,BMG_DS043944,,Deficiency of Platelet Glycoprotein 1b,Bernard-Soulier Syndrome,,,,,,C2713537,D001606,,,,
+BMGC_DS13151,BMG_DS043945,,Androgen Receptor Deficiency,Androgen-Insensitivity Syndrome,,,,,,C2713546,D013734,,,,
+BMGC_DS13152,BMG_DS043949,,Platelet alpha-Granule Deficiency,Gray Platelet Syndrome,,,,,,C2717750,D055652,,,,
+BMGC_DS13153,BMG_DS043952,,Steroid Sulfatase Deficiency Disease,"Ichthyosis, X-Linked",,,,,,C2717836,D016114,,,,
+BMGC_DS13154,BMG_DS043953,,"Drug-Induced Liver Injury, Chronic","Chemical and Drug Induced Liver Injury, Chronic",,,,,,C2717837,D056487,,,,
+BMGC_DS13155,BMG_DS043954,,Encapsulating Peritoneal Sclerosis,Peritoneal Fibrosis,,,,,,C2717860,D056627,,,,
+BMGC_DS13156,BMG_DS043958,,Propionic Aciduria,Propionic Acidemia,,,,DOID:14701,propionic acidemia,C2717876,D056693,,,,
+BMGC_DS13157,BMG_DS043959,,"Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant",Autoimmune Lymphoproliferative Syndrome,,,,,,C2717884,D056735,,MONDO:0017979,autoimmune lymphoproliferative syndrome,
+BMGC_DS13158,BMG_DS043960,,Hereditary Angioedema Types I and II,Hereditary Angioedema Types I and II,,,,,,C2717905,D056829,,,,
+BMGC_DS13159,BMG_DS043961,,Hereditary Angioedema Type I,Hereditary Angioedema Types I and II,,,,,,C2717906,D056829,,MONDO:0015053,hereditary angioedema type 1,
+BMGC_DS13160,BMG_DS043962,,Isolated Noncompaction of the Ventricular Myocardium,Isolated Noncompaction of the Ventricular Myocardium,,,,,,C2717907,D056830,,,,
+BMGC_DS13161,BMG_DS043966,,Thrombotic Microangiopathies,Thrombotic Microangiopathies,,,,,,C2717961,D057049,,MONDO:0019737,thrombotic microangiopathy,
+BMGC_DS13162,BMG_DS043972,,Alcoholic Steatohepatitis,"Fatty Liver, Alcoholic",,,,,,C2718067,D005235,,,,
+BMGC_DS13163,BMG_DS043973,,beta-Galactosidase Deficiency,"Gangliosidosis, GM1",,,,,,C2718068,D016537,,,,
+BMGC_DS13164,BMG_DS043974,,Deficiency of Uroporphyrinogen III Synthase,"Porphyria, Erythropoietic",,,,,,C2718078,D017092,,,,
+BMGC_DS13165,BMG_DS043976,,Sulfoiduronate Sulfatase Deficiency,Mucopolysaccharidosis II,,,,,,C2718304,D016532,,,,
+BMGC_DS13166,BMG_DS043977,,Placental Steroid Sulfatase Deficiency,"Ichthyosis, X-Linked",,,,,,C2720163,D016114,,,,
+BMGC_DS13167,BMG_DS043978,,"ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY",,,,,DOID:0051003,congenital nonspherocytic hemolytic anemia 1,C2720289,,305900;300908,MONDO:0010480,"anemia, nonspherocytic hemolytic, due to G6PD deficiency",
+BMGC_DS13168,BMG_DS043979,73725006;442110002,Fibrosis of pleura,,,,,,,C2720436,,,,,Thickening of pleura | Pleural thickening | Pleural cuirasse | Thickening of pleura (disorder) | Fibrosis of pleura | Pleural fibrosis | Fibrosis of pleura (disorder)
+BMGC_DS13169,BMG_DS043996,443805006,Auditory neuropathy spectrum disorder,,,,,,,C2732267,,,,,Auditory neuropathy spectrum disorder (disorder) | Auditory neuropathy spectrum disorder | Auditory neuropathy with dys-synchrony
+BMGC_DS13170,BMG_DS044037,,Cerebral Small Vessel Diseases,Cerebral Small Vessel Diseases,,,,,,C2733158,D059345,,,,
+BMGC_DS13171,BMG_DS044060,186342000,Pulmonary Mycobacterium avium complex infection,,,,,,,C2733595,,,,,Pulmonary Mycobacterium avium complex infection (disorder) | Pulmonary Mycobacterium avium complex infection | Pulmonary Mycobacterium avium-intracellulare infection
+BMGC_DS13172,BMG_DS044061,443700006,Disorder of lumbar disc,,,,,,,C2733598,,,,,Disorder of lumbar disc (disorder) | Disorder of lumbar disc
+BMGC_DS13173,BMG_DS044069,,Juvenile-Onset Vitelliform Macular Dystrophy,Vitelliform Macular Dystrophy,,,,DOID:0050661,vitelliform macular dystrophy,C2745945,D057826,153700,MONDO:0007931,vitelliform macular dystrophy 2,
+BMGC_DS13174,BMG_DS044070,,"Hyalinosis, Systemic",Hyaline Fibromatosis Syndrome,,,,DOID:0111669,hyaline fibromatosis syndrome,C2745948,D057770,,MONDO:0016071,juvenile hyaline fibromatosis,
+BMGC_DS13175,BMG_DS044071,,Spondylometaphyseal dysplasia with dentinogenesis imperfecta,,,,,,,C2745953,C535792,,MONDO:0031169,odontochondrodysplasia,
+BMGC_DS13176,BMG_DS044072,,,,,,,,,C2745959,,183900,MONDO:0008471,spondyloepiphyseal dysplasia congenita,
+BMGC_DS13177,BMG_DS044074,,Kashin-Beck Disease,Kashin-Beck Disease,,,,,,C2745963,D057767,,MONDO:0005610,Kashin-Beck disease,
+BMGC_DS13178,BMG_DS044075,,Fitzsimmons-McLachlan-Gilbert syndrome,,,,,,,C2745996,C537058,309560,MONDO:0010662,paraplegia-intellectual disability-hyperkeratosis syndrome,
+BMGC_DS13179,BMG_DS044076,,OROFACIODIGITAL SYNDROME VI,,,,,DOID:0060376,Joubert syndrome with orofaciodigital defect,C2745997,,277170;614571,MONDO:0010176,orofaciodigital syndrome type 6,
+BMGC_DS13180,BMG_DS044077,,2-Hydroxyglutaricaciduria,,,,,DOID:0050573,2-hydroxyglutaric aciduria,C2746066,C535306,,MONDO:0016001,2-hydroxyglutaric aciduria,
+BMGC_DS13181,BMG_DS044079,,Congenital idiopathic intestinal pseudoobstruction,,,,,,,C2746068,C535532,300048,MONDO:0010232,"intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked",
+BMGC_DS13182,BMG_DS044080,,Familial ectopia lentis,,,,,DOID:0111148,isolated ectopia lentis,C2746069,C536184,,,,
+BMGC_DS13183,BMG_DS044081,,"Deafness, Autosomal Recessive 77",,,,,,,C2746083,C567543,613079,MONDO:0013119,autosomal recessive nonsyndromic hearing loss 77,
+BMGC_DS13184,BMG_DS044083,,Cronobacter Infections,Enterobacteriaceae Infections,,,,,,C2747880,D004756,,,,
+BMGC_DS13185,BMG_DS044086,,Sensorineural Deafness With Mild Renal Dysfunction,,,,,,,C2748440,C567544,,,,
+BMGC_DS13186,BMG_DS044088,,,,,,,,,C2748501,,602068,MONDO:0011179,"leishmaniasis, tegumentary, susceptibility to",
+BMGC_DS13187,BMG_DS044089,,"CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS",,,,,,,C2748502,,612868,MONDO:0013027,posterior amorphous corneal dystrophy,
+BMGC_DS13188,BMG_DS044092,,Orofacial Cleft 12,,,,,DOID:0080405,orofacial cleft 12,C2748505,C567548,612858,MONDO:0013023,orofacial cleft 12,
+BMGC_DS13189,BMG_DS044093,,,,,,,,,C2748506,,612853,MONDO:0013022,"restless legs syndrome, susceptibility to, 7",
+BMGC_DS13190,BMG_DS044094,,INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY,,,,,,,C2748507,,612852,MONDO:0013021,sterile multifocal osteomyelitis with periostitis and pustulosis,
+BMGC_DS13191,BMG_DS044096,,,,,,,,,C2748515,,612847,MONDO:0019666,"spondyloepimetaphyseal dysplasia, PAPSS2 type",
+BMGC_DS13192,BMG_DS044098,,Lumbar scoliosis,,,,,,,C2748518,,MTHU024856,,,
+BMGC_DS13193,BMG_DS044099,,"Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant",,,,,,,C2748527,C567553,612843,MONDO:0013018,"keratosis follicularis spinulosa decalvans, autosomal dominant",
+BMGC_DS13194,BMG_DS044100,,Hypotrichosis 5,,,,,DOID:0110702,hypotrichosis 5,C2748535,C567554,612841,MONDO:0013017,hypotrichosis 5,
+BMGC_DS13195,BMG_DS044101,,"Leukocyte Adhesion Deficiency, Type III",,,,,,,C2748536,C567555,612840,MONDO:0013016,leukocyte adhesion deficiency 3,
+BMGC_DS13196,BMG_DS044102,,Brugada Syndrome 5,,,,,DOID:0110222,Brugada syndrome 5,C2748541,C567556,612838,MONDO:0013015,Brugada syndrome 5,
+BMGC_DS13197,BMG_DS044103,,"Cardiac Conduction Defect, Nonspecific",,,,,,,C2748542,C567557,,MONDO:0005449,conduction system disorder,
+BMGC_DS13198,BMG_DS044104,,"Spondyloepimetaphyseal Dysplasia, Aggrecan Type",,,,,,,C2748544,C567558,612813,MONDO:0013014,"spondyloepimetaphyseal dysplasia, aggrecan type",
+BMGC_DS13199,BMG_DS044105,,,,,,,,,C2748545,,612798,MONDO:0013013,"question mark ears, isolated",
+BMGC_DS13200,BMG_DS044106,,Inflammatory Bowel Disease 27,,,,,DOID:0110902,inflammatory bowel disease 27,C2748550,C567559,612796,MONDO:0013012,inflammatory bowel disease 27,
+BMGC_DS13201,BMG_DS044107,,Atrial Septal Defect 5,,,,,,,C2748552,C567561,612794,MONDO:0013011,atrial septal defect 5,
+BMGC_DS13202,BMG_DS044108,,"Deafness, Autosomal Recessive 71",,,,,,,C2748554,C567562,612789,MONDO:0013010,autosomal recessive nonsyndromic hearing loss 71,
+BMGC_DS13203,BMG_DS044110,,Immune dysfunction with T-cell inactivation due to calcium entry defect 2,,,,,DOID:0111970,immunodeficiency 10,C2748557,C557827,612783,MONDO:0013008,combined immunodeficiency due to STIM1 deficiency,
+BMGC_DS13204,BMG_DS044111,,Immune dysfunction with T-cell inactivation due to calcium entry defect 1,,,,,DOID:0111976,immunodeficiency 9,C2748568,C557826,612782,MONDO:0013007,combined immunodeficiency due to ORAI1 deficiency,
+BMGC_DS13205,BMG_DS044112,,"Isolated Growth Hormone Deficiency, Type IB",,,,,,,C2748571,C567564,612781,MONDO:0013006,isolated growth hormone deficiency type IB,
+BMGC_DS13206,BMG_DS044113,,SeSAME syndrome,,,,,DOID:0060484,EAST syndrome,C2748572,C557674,612780,MONDO:0013005,EAST syndrome,
+BMGC_DS13207,BMG_DS044115,,Hypoglossia With Situs Inversus,,,,,,,C2748587,C567567,612776,MONDO:0013003,isolated congenital hypoglossia/aglossia,
+BMGC_DS13208,BMG_DS044119,,Mitchell-Riley Syndrome,,,,,,,C2748662,C567570,615710,MONDO:0017400,hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome,
+BMGC_DS13209,BMG_DS044121,,"Vitamin D-Dependent Rickets, Type 2B, With Normal Vitamin D Receptor",,,,,,,C2748783,C567571,600785,MONDO:0010931,"vitamin D-dependent rickets, type 2B",
+BMGC_DS13210,BMG_DS044123,,"FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULAR INVOLVEMENT",,,,,DOID:0081017,congenital fibrosis of the extraocular muscles 3A,C2748801,,600638;602661,MONDO:0010912,"fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement",
+BMGC_DS13211,BMG_DS044124,,"CARDIOMYOPATHY, INFANTILE HYPERTROPHIC",,,,,DOID:0111753,infantile hypertrophic cardiomyopathy,C2748884,,500006;516060;516070,MONDO:0010777,"cardiomyopathy, infantile hypertrophic",
+BMGC_DS13212,BMG_DS044125,,Ovotesticular Disorders of Sex Development,Ovotesticular Disorders of Sex Development,,,,,,C2748895,D050090,400045,MONDO:0100250,"46,XX sex reversal 1",
+BMGC_DS13213,BMG_DS044126,,"46,Xy Gonadal Dysgenesis, Complete, Sry-Related",,,,,,,C2748896,C567574,400044,MONDO:0020712,"46,XY sex reversal 1",
+BMGC_DS13214,BMG_DS044127,,"46,Xy True Hermaphroditism, Sry-Related",,,,,,,C2748897,C567575,,,,
+BMGC_DS13215,BMG_DS044128,,"Rett Syndrome, Atypical",,,,,,,C2748910,C567576,,MONDO:0017746,atypical Rett syndrome,
+BMGC_DS13216,BMG_DS044129,,Otopalatodigital Spectrum Disorder,,,,,,,C2748918,C567577,,MONDO:0018233,otopalatodigital syndrome spectrum disorder,
+BMGC_DS13217,BMG_DS044131,,"Glycogen Storage Disease, Type IXA2",,,,,,,C2748941,C567579,,MONDO:0100439,glycogen storage disease IXa2,
+BMGC_DS13218,BMG_DS044132,,Chromosome Xq28 Duplication Syndrome,,,,,,,C2749007,C567580,300815,MONDO:0010436,chromosome Xq28 duplication syndrome,
+BMGC_DS13219,BMG_DS044134,,"Thrombophilia, X-Linked, Due To Factor Ix Defect",,,,,DOID:0111899,X-linked thrombophilia due to factor IX defect,C2749016,C567581,300807,MONDO:0010432,"thrombophilia, X-linked, due to factor 9 defect",
+BMGC_DS13220,BMG_DS044135,,Joubert Syndrome 10,,,,,DOID:0110981,Joubert syndrome 10,C2749019,C567582,300804,MONDO:0010431,Joubert syndrome 10,
+BMGC_DS13221,BMG_DS044136,,,,,,,,,C2749020,,300803,MONDO:0010430,"intellectual disability, X-linked 97",
+BMGC_DS13222,BMG_DS044137,,Chromosome Xp11.23-P11.22 Duplication Syndrome,,,,,DOID:0060461,chromosome Xp11.23-p11.22 duplication syndrome,C2749022,C567585,300801,MONDO:0010428,chromosome Xp11.23-p11.22 duplication syndrome,
+BMGC_DS13223,BMG_DS044138,,"Corneal Dystrophy, Endothelial, X-Linked",,,,,DOID:0060446,X-linked endothelial corneal dystrophy,C2749049,C567587,300779,MONDO:0010426,X-linked endothelial corneal dystrophy,
+BMGC_DS13224,BMG_DS044139,,"Corneal Dystrophy, Lisch Epithelial",,,,,DOID:0060450,Lisch epithelial corneal dystrophy,C2749050,C567588,620763;300778,MONDO:0010425,Lisch epithelial corneal dystrophy,
+BMGC_DS13225,BMG_DS044140,,"Emery-Dreifuss Muscular Dystrophy 6, X-Linked",X-Linked Emery-Dreifuss Muscular Dystrophy,,,,,,C2749106,D000083143,,MONDO:0800318,"Emery-Dreifuss muscular dystrophy 6, X-linked",
+BMGC_DS13226,BMG_DS044141,,"Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked",,,,,,,C2749128,C567594,300580,MONDO:0010365,"myopathy, congenital, with fiber-type disproportion, X-linked",
+BMGC_DS13227,BMG_DS044142,,"Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness",,,,,,,C2749137,C567595,300455,MONDO:0010330,obsolete primary ciliary dyskinesia-retinitis pigmentosa syndrome,
+BMGC_DS13228,BMG_DS044143,,"Mineralocorticoid Deficiency, Isolated",,,,,,,C2749175,C567596,,,,
+BMGC_DS13229,BMG_DS044144,,"46,XX SEX REVERSAL 2",,,,,DOID:0111763,"46,XX sex reversal 2",C2749215,,278850;608160,MONDO:0010218,"46,XX sex reversal 2",
+BMGC_DS13230,BMG_DS044145,,Vater Association With Macrocephaly And Ventriculomegaly,,,,,,,C2749240,C564752,,,,
+BMGC_DS13231,BMG_DS044146,,"Gm2-Gangliosidosis, Variant B1",,,,,,,C2749283,C567601,,,,
+BMGC_DS13232,BMG_DS044148,,"Refsum Disease, Adult, 1",,,,,,,C2749345,C567602,,,,
+BMGC_DS13233,BMG_DS044149,,"Refsum Disease, Adult, 2",,,,,,,C2749346,C567603,614879,MONDO:0013945,peroxisome biogenesis disorder 9B,
+BMGC_DS13234,BMG_DS044150,,"Oculodentodigital Dysplasia, Autosomal Recessive",,,,,,,C2749477,C567605,257850,MONDO:0009768,"oculodentodigital dysplasia, autosomal recessive",
+BMGC_DS13235,BMG_DS044151,,,,,,,,,C2749485,,256700,MONDO:0009741,"neuroblastoma, susceptibility to, 1",
+BMGC_DS13236,BMG_DS044152,,"MYOPIA 18, AUTOSOMAL RECESSIVE",,,,,,,C2749509,,255500,MONDO:0009713,"myopia 18, autosomal recessive",
+BMGC_DS13237,BMG_DS044154,,"Methemoglobinemia, Type I",,,,,,,C2749559,C537841,,,,
+BMGC_DS13238,BMG_DS044155,,"Methemoglobinemia, Type Ii",,,,,,,C2749560,C537841,,,,
+BMGC_DS13239,BMG_DS044156,,"Nadh-Cytochrome B5 Reductase Deficiency, Type I",,,,,,,C2749561,C537841,,,,
+BMGC_DS13240,BMG_DS044157,,"Nadh-Cytochrome B5 Reductase Deficiency, Type Ii",,,,,,,C2749562,C537841,,,,
+BMGC_DS13241,BMG_DS044159,,"AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I, WITH REVERSIBLE METAPHYSEAL DYSPLASIA",,,,,,,C2749602,,607358,,,
+BMGC_DS13242,BMG_DS044160,,,,,,,,,C2749604,,235400,MONDO:0009335,"hemolytic uremic syndrome, atypical, susceptibility to, 1",
+BMGC_DS13243,BMG_DS044161,,Motor axonal neuropathy,,,,,,,C2749625,,MTHU026112,,,
+BMGC_DS13244,BMG_DS044163,,"MEGALOBLASTIC ANEMIA, FOLATE-RESPONSIVE",,,,,,,C2749656,,600424;601775,MONDO:0011141,"megaloblastic anemia, folate-responsive",
+BMGC_DS13245,BMG_DS044164,,Aicardi-Goutieres syndrome 5,,,,,,,C2749659,C535608,612952,MONDO:0013059,Aicardi-Goutieres syndrome 5,
+BMGC_DS13246,BMG_DS044165,,Split-Hand-Foot Malformation 6,,,,,,,C2749665,C567616,225300,MONDO:0009157,split hand-foot malformation 6,
+BMGC_DS13247,BMG_DS044167,,"CYSTINOSIS, ATYPICAL NEPHROPATHIC",,,,,,,C2749685,,219800;606272,,,
+BMGC_DS13248,BMG_DS044168,,BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1,,,,,DOID:0080526,bronchiectasis 1,C2749757,,211400;600760,MONDO:0008887,bronchiectasis with or without elevated sweat chloride 1,
+BMGC_DS13249,BMG_DS044169,,"Macrothrombocytopenia-Stomatocytosis, Mediterranean",,,,,,,C2749759,C537345,210250,MONDO:0020747,sitosterolemia 1,
+BMGC_DS13250,BMG_DS044172,,MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY),,,,,,,C2749861,,604712;612075,MONDO:0012792,mitochondrial DNA depletion syndrome 8a,
+BMGC_DS13251,BMG_DS044173,,"Mitochondrial Neurogastrointestinal Encephalopathy Syndrome, Rrm2b-Related",,,,,DOID:0080127;DOID:0070331;DOID:0080119,mitochondrial DNA depletion syndrome 8b | mitochondrial DNA depletion syndrome 8a | mitochondrial DNA depletion syndrome 1,C2749862,C536350,,,,
+BMGC_DS13252,BMG_DS044174,1197052008,Mitochondrial DNA depletion syndrome encephalomyopathic form with methylmalonic aciduria,,,,,,,C2749864,,612073,MONDO:0012791,"mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria",Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with methylmalonic aciduria (disorder) | Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with methylmalonic aciduria | Mitochondrial DNA depletion syndrome encephalomyopathic form with methylmalonic aciduria | Mitochondrial encephalomyopathy aminoacidopathy syndrome | mtDNA (mitochondrial deoxyribonucleic acid) depletion syndrome encephalomyopathic form with methylmalonic aciduria | Booth Haworth Dilling syndrome
+BMGC_DS13253,BMG_DS044175,,,,,,,,,C2749872,,611942,MONDO:0012763,"epilepsy, childhood absence, susceptibility to, 6",
+BMGC_DS13254,BMG_DS044176,,Chromosome 3q29 Duplication Syndrome,,,,,DOID:0060459,chromosome 3q29 microduplication syndrome,C2749873,C567626,611936,MONDO:0012761,chromosome 3q29 microduplication syndrome,
+BMGC_DS13255,BMG_DS044178,,"Spastic Paraplegia 18, Autosomal Recessive",,,,,,,C2749936,C567628,611225,MONDO:0012639,hereditary spastic paraplegia 18,
+BMGC_DS13256,BMG_DS044179,,,,,,,,,C2749982,,188580,MONDO:0008570,"thyrotoxic periodic paralysis, susceptibility to, 1",
+BMGC_DS13257,BMG_DS044180,,Growth Hormone Deficiency With Pituitary Anomalies,,,,,,,C2750027,C567632,,,,
+BMGC_DS13258,BMG_DS044182,,"Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive",,,,,,,C2750035,C567633,616516,MONDO:0014676,"Emery-Dreifuss muscular dystrophy 3, autosomal recessive",
+BMGC_DS13259,BMG_DS044184,,"Hypokalemic Periodic Paralysis, Type 2",,,,,,,C2750061,C567635,613345,MONDO:0013234,"hypokalemic periodic paralysis, type 2",
+BMGC_DS13260,BMG_DS044185,,Leber Congenital Amaurosis 14,,,,,DOID:0110188,Leber congenital amaurosis 14,C2750063,C567636,613341,MONDO:0013231,Leber congenital amaurosis 14,
+BMGC_DS13261,BMG_DS044186,,"Retinal Dystrophy, Early-Onset Severe, Lrat-Related",,,,,DOID:0110188,Leber congenital amaurosis 14,C2750064,C567636,,,,
+BMGC_DS13262,BMG_DS044187,,"RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED",,,,,,,C2750065,,613341;604863,,,
+BMGC_DS13263,BMG_DS044188,,Spondylo-Megaepiphyseal-Metaphyseal Dysplasia,,,,,,,C2750066,C567639,613330,MONDO:0013228,spondylo-megaepiphyseal-metaphyseal dysplasia,
+BMGC_DS13264,BMG_DS044189,,Plasminogen Activator Inhibitor-1 Deficiency,,,,,,,C2750067,C567640,613329,MONDO:0013227,congenital plasminogen activator inhibitor type 1 deficiency,
+BMGC_DS13265,BMG_DS044190,,Roifman-Chitayat Syndrome,,,,,,,C2750068,C567641,613328,MONDO:0013226,combined immunodeficiency with faciooculoskeletal anomalies,
+BMGC_DS13266,BMG_DS044191,,"Lipodystrophy, Congenital Generalized, Type 4",,,,,,,C2750069,C567642,613327,MONDO:0013225,congenital generalized lipodystrophy type 4,
+BMGC_DS13267,BMG_DS044192,,Rhabdoid Tumor Predisposition Syndrome 2,,,,,,,C2750074,C567643,613325,MONDO:0013224,rhabdoid tumor predisposition syndrome 2,
+BMGC_DS13268,BMG_DS044193,,"Chondrodysplasia, Megarbane-Dagher-Melki Type",,,,,,,C2750075,C567644,613320,MONDO:0013223,"autosomal recessive spondylometaphyseal dysplasia, Megarbane type",
+BMGC_DS13269,BMG_DS044194,,Miyoshi Muscular Dystrophy 3,,,,,DOID:0070201,Miyoshi muscular dystrophy 3,C2750076,C567645,613319,MONDO:0013222,Miyoshi muscular dystrophy 3,
+BMGC_DS13270,BMG_DS044195,,Miyoshi Muscular Dystrophy 2,,,,,DOID:0070200,Miyoshi muscular dystrophy 2,C2750077,C567646,613318,MONDO:0013221,Miyoshi muscular dystrophy 2,
+BMGC_DS13271,BMG_DS044196,,"Hypophosphatemic Rickets, Autosomal Recessive, 2",,,,,,,C2750078,C567647,613312,MONDO:0013219,"hypophosphatemic rickets, autosomal recessive, 2",
+BMGC_DS13272,BMG_DS044197,,Exudative Vitreoretinopathy 5,,,,,DOID:0111408,exudative vitreoretinopathy 5,C2750079,C567648,613310,MONDO:0013218,exudative vitreoretinopathy 5,
+BMGC_DS13273,BMG_DS044198,,Diamond-Blackfan Anemia 10,,,,,DOID:0111888,Diamond-Blackfan anemia 10,C2750080,C567649,613309,MONDO:0013217,Diamond-Blackfan anemia 10,
+BMGC_DS13274,BMG_DS044199,,Diamond-Blackfan Anemia 9,,,,,DOID:0111884,Diamond-Blackfan anemia 9,C2750081,C567650,613308,MONDO:0013216,Diamond-Blackfan anemia 9,
+BMGC_DS13275,BMG_DS044200,,"Deafness, Autosomal Recessive 79",,,,,,,C2750082,C567651,613307,MONDO:0013215,autosomal recessive nonsyndromic hearing loss 79,
+BMGC_DS13276,BMG_DS044201,,"Bile Acid Malabsorption, Primary",,,,,,,C2750087,C567652,,,,
+BMGC_DS13277,BMG_DS044203,,"Charcot-Marie-Tooth Disease, Axonal, Type 2n",,,,,,,C2750090,C567653,613287,MONDO:0013212,Charcot-Marie-Tooth disease axonal type 2N,
+BMGC_DS13278,BMG_DS044204,,"Cardiomyopathy, Dilated, 1FF",,,,,,,C2750091,C567654,613286,MONDO:0013211,dilated cardiomyopathy 1FF,
+BMGC_DS13279,BMG_DS044205,,,,,,,,,C2750180,,610551,MONDO:0024563,"herpes simplex encephalitis, susceptibility to, 1",
+BMGC_DS13280,BMG_DS044206,,Karak Syndrome,,,,,,,C2750220,C548029,,,,
+BMGC_DS13281,BMG_DS044207,,"CEREBELLAR ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSEQUILIBRIUM SYNDROME 2",,,,,DOID:0070557,"cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 2",C2750234,,610185;614218,MONDO:0012430,"cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 2",
+BMGC_DS13282,BMG_DS044208,,Pitt-Hopkins-Like Syndrome 1,,,,,DOID:0090130,cortical dysplasia-focal epilepsy syndrome,C2750246,C567657,610042,MONDO:0012400,cortical dysplasia-focal epilepsy syndrome,
+BMGC_DS13283,BMG_DS044210,,"Progeria Syndrome, Childhood-Onset",,,,,,,C2750285,C567661,,,,
+BMGC_DS13284,BMG_DS044211,770944002,Oculootodental syndrome,,,,,,,C2750325,,,MONDO:0020494,oculootodental syndrome,Oculootodental syndrome | Oculootodental syndrome (disorder)
+BMGC_DS13285,BMG_DS044212,725165009,Omodysplasia 2,,,,,DOID:0080845,omodysplasia 2,C2750355,C567664,164745,MONDO:0008123,autosomal dominant omodysplasia,Autosomal dominant omodysplasia (disorder) | Autosomal dominant omodysplasia | Omodysplasia 2
+BMGC_DS13286,BMG_DS044213,,"Fibrosis of Extraocular Muscles, Congenital, 3C",,,,,,,C2750404,C567666,609384,MONDO:0012262,"fibrosis of extraocular muscles, congenital, 3c",
+BMGC_DS13287,BMG_DS044214,,"Cap Myopathy, Tpm2-Related",,,,,DOID:0110932,nemaline myopathy 4,C2750413,C538351,,,,
+BMGC_DS13288,BMG_DS044215,,"Cap Myopathy, Tpm3-Related",,,,,DOID:0110926,nemaline myopathy 1,C2750414,C538348,,,,
+BMGC_DS13289,BMG_DS044216,,Bifid Nose With Or Without Anorectal And Renal Anomalies,,,,,,,C2750433,C567672,608980,MONDO:0012165,BNAR syndrome,
+BMGC_DS13290,BMG_DS044217,,,,,,,,,C2750440,,613282,MONDO:0021105,NAFLD1,
+BMGC_DS13291,BMG_DS044218,,Hypermanganesemia with Dystonia Polycythemia and Cirrhosis,,,,,,,C2750442,C548016,613280,MONDO:0013208,cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome,
+BMGC_DS13292,BMG_DS044220,,"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6",,,,,,,C2750448,,189909;613270,MONDO:0013206,"corneal dystrophy, Fuchs endothelial, 6",
+BMGC_DS13293,BMG_DS044222,,"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4",,,,,,,C2750450,,610206;613268,MONDO:0013204,"corneal dystrophy, Fuchs endothelial, 4",
+BMGC_DS13294,BMG_DS044223,,"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3",,,,,,,C2750451,,613267;602272,MONDO:0013203,"corneal dystrophy, Fuchs endothelial, 3",
+BMGC_DS13295,BMG_DS044224,,"Waardenburg Syndrome, Type 4c",,,,,,,C2750452,C567679,613266,MONDO:0013202,Waardenburg syndrome type 4C,
+BMGC_DS13296,BMG_DS044225,,"Waardenburg Syndrome, Type 4b",,,,,,,C2750457,C567680,613265,MONDO:0013201,Waardenburg syndrome type 4B,
+BMGC_DS13297,BMG_DS044226,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 15",,,,,DOID:0110321,hypertrophic cardiomyopathy 15,C2750459,,193065;613255,MONDO:0013200,hypertrophic cardiomyopathy 15,
+BMGC_DS13298,BMG_DS044227,,"Cardiomyopathy, Dilated, 1EE",,,,,,,C2750466,C567683,613252,MONDO:0013198,dilated cardiomyopathy 1EE,
+BMGC_DS13299,BMG_DS044228,,"Cardiomyopathy, Familial Hypertrophic, 14",,,,,,,C2750467,C567684,613251,MONDO:0013197,hypertrophic cardiomyopathy 14,
+BMGC_DS13300,BMG_DS044229,,"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 8",,,,,DOID:0070270,hereditary nonpolyposis colorectal cancer type 8,C2750471,,613244,MONDO:0013196,Lynch syndrome 8,
+BMGC_DS13301,BMG_DS044230,,"Cardiomyopathy, Familial Hypertrophic, 13",,,,,,,C2750472,C567686,613243,MONDO:0013195,hypertrophic cardiomyopathy 13,
+BMGC_DS13302,BMG_DS044231,,,,,,,,,C2750473,,613239,MONDO:0013193,"thyrotoxic periodic paralysis, susceptibility to, 2",
+BMGC_DS13303,BMG_DS044233,,Focal Segmental Glomerulosclerosis 5,,,,,DOID:0111130,focal segmental glomerulosclerosis 5,C2750475,C567687,613237,MONDO:0013191,focal segmental glomerulosclerosis 5,
+BMGC_DS13304,BMG_DS044234,,,,,,,,,C2750481,,613235,MONDO:0013190,"factor XIII, b subunit, deficiency of",
+BMGC_DS13305,BMG_DS044235,,"Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3",,,,,DOID:0070558,autosomal recessive spinocerebellar ataxia 34,C2750509,C567690,613227,MONDO:0013188,"cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 3",
+BMGC_DS13306,BMG_DS044236,,"Factor Xiii, A Subunit, Deficiency Of",,,,,,,C2750514,C567691,613225,MONDO:0013187,"factor XIII, A subunit, deficiency of",
+BMGC_DS13307,BMG_DS044237,,,,,,,,,C2750548,,161550,MONDO:0008067,"nasopharyngeal carcinoma, susceptibility to, 2",
+BMGC_DS13308,BMG_DS044238,,Cone-Rod Dystrophy 13,,,,,DOID:0111016,cone-rod dystrophy 13,C2750720,C567698,608194,MONDO:0011987,cone-rod dystrophy 13,
+BMGC_DS13309,BMG_DS044239,,"Amyotrophic Lateral Sclerosis 6, Autosomal Recessive",,,,,,,C2750729,C567699,,,,
+BMGC_DS13310,BMG_DS044240,,Noonan Syndrome 6,,,,,DOID:0060584,Noonan syndrome 6,C2750732,C548084,613224,MONDO:0013186,Noonan syndrome 6,
+BMGC_DS13311,BMG_DS044241,,,,,,,,,C2750733,,613223,MONDO:0013185,"leprosy, susceptibility to, 5",
+BMGC_DS13312,BMG_DS044242,,"DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL",,,,,,,C2750737,,613217;185535,MONDO:0013184,congenital diarrhea 5 with tufting enteropathy,
+BMGC_DS13313,BMG_DS044244,,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C",,,,,DOID:0110867,congenital stationary night blindness 1C,C2750747,,613216;603576,MONDO:0013183,congenital stationary night blindness 1C,
+BMGC_DS13314,BMG_DS044246,,"Amelogenesis Imperfecta, Hypomaturation Type, Iia3",,,,,,,C2750771,C567706,613211,MONDO:0013181,amelogenesis imperfecta hypomaturation type 2A3,
+BMGC_DS13315,BMG_DS044248,,"Spastic Paraplegia 44, Autosomal Recessive",,,,,,,C2750784,C567707,613206,MONDO:0013179,hereditary spastic paraplegia 44,
+BMGC_DS13316,BMG_DS044249,,"Muscular Dystrophy, Congenital, Lmna-Related",,,,,,,C2750785,C567708,613205,MONDO:0013178,congenital muscular dystrophy due to LMNA mutation,
+BMGC_DS13317,BMG_DS044250,,"Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency",,,,,,,C2750786,C567709,613204,MONDO:0013177,congenital muscular dystrophy due to integrin alpha-7 deficiency,
+BMGC_DS13318,BMG_DS044251,,Weill-Marchesani-Like Syndrome,,,,,,,C2750787,C567710,613195,MONDO:0013176,"Weill-Marchesani 4 syndrome, recessive",
+BMGC_DS13319,BMG_DS044252,,"Retinitis Pigmentosa, Concentric",,,,,,,C2750789,C567712,613194,MONDO:0013175,retinitis pigmentosa 50,
+BMGC_DS13320,BMG_DS044253,,"CILIARY DYSKINESIA, PRIMARY, 13",,,,,,,C2750790,,613193;613190,MONDO:0013174,primary ciliary dyskinesia 13,
+BMGC_DS13321,BMG_DS044254,,,,,,,,,C2750791,,613192,MONDO:0013173,"intellectual disability, autosomal recessive 13",
+BMGC_DS13322,BMG_DS044255,,Polymicrogyria With Optic Nerve Hypoplasia,,,,,,,C2750798,C567715,613180,MONDO:0013172,polymicrogyria with optic nerve hypoplasia,
+BMGC_DS13323,BMG_DS044256,,"Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities",,,,,DOID:0070139,autosomal recessive cutis laxa type IC,C2750804,C567716,613177,MONDO:0013170,"cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies",
+BMGC_DS13324,BMG_DS044257,,Chromosome 5p13 Duplication Syndrome,,,,,DOID:0060460,chromosome 5p13 duplication syndrome,C2750805,C567717,613174,MONDO:0013169,chromosome 5p13 duplication syndrome,
+BMGC_DS13325,BMG_DS044258,,Marie Unna Hereditary Hypotrichosis 1,,,,,,,C2750815,C567718,146550,MONDO:0100522,hypotrichosis 4,
+BMGC_DS13326,BMG_DS044259,,Dystransthyretinemic Euthyroidal Hyperthyroxinemia,,,,,,,C2750824,C567719,145680,MONDO:0007785,"hyperthyroxinemia, dystransthyretinemic",
+BMGC_DS13327,BMG_DS044260,,,,,,,,,C2750850,,137800,MONDO:0024498,glioma susceptibility 1,
+BMGC_DS13328,BMG_DS044261,,,,,,,,,C2750887,,607682,MONDO:0011892,"epilepsy, idiopathic generalized, susceptibility to, 9",
+BMGC_DS13329,BMG_DS044262,,,,,,,,,C2750888,,,MONDO:0800271,"epilepsy, juvenile myoclonic, susceptibility to, 6",
+BMGC_DS13330,BMG_DS044263,,,,,,,,,C2750892,,607631,MONDO:0020772,"epilepsy, juvenile absence, susceptibility to, 1",
+BMGC_DS13331,BMG_DS044264,,,,,,,,,C2750893,,607628,MONDO:0011875,"epilepsy, idiopathic generalized, susceptibility to, 11",
+BMGC_DS13332,BMG_DS044266,,"Cardiomyopathy, Dilated, 1DD",,,,,,,C2750995,C567725,613172,MONDO:0013168,dilated cardiomyopathy 1DD,
+BMGC_DS13333,BMG_DS044268,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 4",,,,,DOID:0112379,muscular dystrophy-dystroglycanopathy type B4,C2751052,,613152;607440,MONDO:0013156,"muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4",
+BMGC_DS13334,BMG_DS044269,,"INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE",,,,,DOID:0110899,inflammatory bowel disease 28,C2751053,,613148,MONDO:0013153,inflammatory bowel disease 28,
+BMGC_DS13335,BMG_DS044271,,"Choroidal Dystrophy, Central Areolar 3",,,,,,,C2751055,C567729,613144,MONDO:0013151,"choroidal dystrophy, central areolar, 3",
+BMGC_DS13336,BMG_DS044272,,"Parkinsonism-Dystonia, Infantile",,,,,DOID:0070489,classic dopamine transporter deficiency syndrome,C2751067,C567730,,MONDO:0013150,"parkinsonism-dystonia, infantile",
+BMGC_DS13337,BMG_DS044274,,Brugada Syndrome 8,,,,,DOID:0110225,Brugada syndrome 8,C2751083,C567732,613123,MONDO:0013148,Brugada syndrome 8,
+BMGC_DS13338,BMG_DS044275,,"Cardiomyopathy, Dilated, 1CC",,,,,,,C2751084,C567733,613122,MONDO:0013147,dilated cardiomyopathy 1CC,
+BMGC_DS13339,BMG_DS044276,,Brugada Syndrome 7,,,,,DOID:0110224,Brugada syndrome 7,C2751088,C567734,613120,MONDO:0013146,Brugada syndrome 7,
+BMGC_DS13340,BMG_DS044277,,Brugada Syndrome 6,,,,,DOID:0110223,Brugada syndrome 6,C2751089,C567735,613119,MONDO:0013145,Brugada syndrome 6,
+BMGC_DS13341,BMG_DS044278,,Thrombophilia Due To Histidine-Rich Glycoprotein Deficiency,,,,,DOID:0111903,thrombophilia due to HRG deficiency,C2751090,C567737,613116,MONDO:0013143,hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency,
+BMGC_DS13342,BMG_DS044279,,Thrombophilia Due To Elevated Histidine-Rich Glycoprotein,,,,,,,C2751091,C567737,,,,
+BMGC_DS13343,BMG_DS044280,,"Neuropathy, Hereditary Sensory And Autonomic, Type IIB",,,,,,,C2751092,C567738,613115,MONDO:0013142,"neuropathy, hereditary sensory and autonomic, type 2B",
+BMGC_DS13344,BMG_DS044281,,"Fibrosis of Extraocular Muscles, Congenital, 3B",,,,,,,C2751105,C567739,,MONDO:0800209,"fibrosis of extraocular muscles, congenital, 3b",
+BMGC_DS13345,BMG_DS044284,,"Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related",,,,,,,C2751259,C567747,,,,
+BMGC_DS13346,BMG_DS044285,,Macrothrombocytopenia,,,,,,,C2751260,,MTHU024610,,,
+BMGC_DS13347,BMG_DS044286,,"Neutropenia, Severe Congenital, Autosomal Dominant 2",,,,,,,C2751288,C567748,613107,MONDO:0013139,"neutropenia, severe congenital, 2, autosomal dominant",
+BMGC_DS13348,BMG_DS044288,,"CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2",,,,,,,C2751290,,613105,MONDO:0013137,"choroidal dystrophy, central areolar 2",
+BMGC_DS13349,BMG_DS044289,,Hypotrichosis And Recurrent Skin Vesicles,,,,,,,C2751292,C567751,613102,MONDO:0013136,hereditary hypotrichosis with recurrent skin vesicles,
+BMGC_DS13350,BMG_DS044290,,,,,,,,,C2751293,,613101,MONDO:0013135,familial hemophagocytic lymphohistiocytosis 5,
+BMGC_DS13351,BMG_DS044291,,"GLAUCOMA 1, OPEN ANGLE, O",,,,,,,C2751294,,162662;613100,MONDO:0013134,"glaucoma 1, open angle, O",
+BMGC_DS13352,BMG_DS044292,,,,,,,,,C2751295,,613099,MONDO:0013133,"melanoma, cutaneous malignant, susceptibility to, 5",
+BMGC_DS13353,BMG_DS044293,,"INCREASED ANALGESIA FROM KAPPA-OPIOID RECEPTOR AGONIST, FEMALE-SPECIFIC",,,,,,,C2751296,,155555;613098,,,
+BMGC_DS13354,BMG_DS044294,,"Tooth Agenesis, Selective, 6",,,,,,,C2751297,C567755,,,,
+BMGC_DS13355,BMG_DS044295,,,,,,,,,C2751306,,613095,MONDO:0013131,polycystic kidney disease 2,
+BMGC_DS13356,BMG_DS044296,,"Microphthalmia, Isolated 4",,,,,,,C2751307,C567757,613094,MONDO:0013130,isolated microphthalmia 4,
+BMGC_DS13357,BMG_DS044297,,Cone Dystrophy 4,,,,,,,C2751308,C567758,613093,MONDO:0013129,cone dystrophy 4,
+BMGC_DS13358,BMG_DS044298,,Achromatopsia 5,,,,,,,C2751309,C567759,,MONDO:0800196,achromatopsia 5,
+BMGC_DS13359,BMG_DS044299,,"Hyperuricemic Nephropathy, Familial Juvenile 2",,,,,,,C2751310,C567760,613092,MONDO:0013128,familial juvenile hyperuricemic nephropathy type 2,
+BMGC_DS13360,BMG_DS044301,,CLAPO Syndrome,,,,,,,C2751313,C567763,613089,MONDO:0013125,CLAPO syndrome,
+BMGC_DS13361,BMG_DS044303,,,,,,,,,C2751315,,613087,MONDO:0013123,atrial septal defect 6,
+BMGC_DS13362,BMG_DS044304,,"Glaucoma 3, Primary Congenital, D",,,,,,,C2751316,C567765,613086,MONDO:0013122,"glaucoma 3, primary congenital, D",
+BMGC_DS13363,BMG_DS044305,,"46, XY Sex Reversal 5",,,,,DOID:0111776,"46,XY sex reversal 5",C2751317,C567766,613080,MONDO:0013120,"46,XY sex reversal 5",
+BMGC_DS13364,BMG_DS044306,,Nijmegen Breakage Syndrome-Like Disorder,,,,,,,C2751318,C567767,613078,MONDO:0013118,Nijmegen breakage syndrome-like disorder,
+BMGC_DS13365,BMG_DS044307,,"Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5",,,,,,,C2751319,C567768,613077,MONDO:0013117,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5",
+BMGC_DS13366,BMG_DS044308,,"Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay",,,,,,,C2751320,C567769,613076,MONDO:0013116,congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome,
+BMGC_DS13367,BMG_DS044309,,"Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis",,,,,,,C2751321,C567770,613075,MONDO:0013115,RIN2 syndrome,
+BMGC_DS13368,BMG_DS044310,,Metaphyseal Anadysplasia 2,,,,,,,C2751322,C567771,613073,MONDO:0013113,metaphyseal anadysplasia 2,
+BMGC_DS13369,BMG_DS044311,,BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3,,,,,DOID:0080528,bronchiectasis 3,C2751324,,600761;613071,MONDO:0013112,bronchiectasis with or without elevated sweat chloride 3,
+BMGC_DS13370,BMG_DS044312,,"46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy",,,,,,,C2751325,C567773,,,,
+BMGC_DS13371,BMG_DS044313,,"PULMONARY DISEASE, CHRONIC OBSTRUCTIVE, RATE OF DECLINE OF LUNG FUNCTION IN",,,,,,,C2751329,,606963,,,
+BMGC_DS13372,BMG_DS044314,,,,,,,,,C2751427,,,MONDO:0800421,"cardiomyopathy, familial hypertrophic, 4, susceptibility to",
+BMGC_DS13373,BMG_DS044315,,"CANDIDIASIS, FAMILIAL, 1",,,,,,,C2751429,,114580,MONDO:0007257,"candidiasis, familial, 1",
+BMGC_DS13374,BMG_DS044316,,Camptodactyly 1,,,,,,,C2751430,C567780,114200,MONDO:0007250,camptodactyly of fingers,
+BMGC_DS13375,BMG_DS044317,,"Bifid Nose, Autosomal Dominant",,,,,,,C2751431,C535441,109740,MONDO:0007195,"bifid nose, autosomal dominant",
+BMGC_DS13376,BMG_DS044318,,,,,,,,,C2751492,,105210,MONDO:0971004,"amyloidosis, hereditary systemic 1",
+BMGC_DS13377,BMG_DS044319,,"Cerebral Amyloid Angiopathy, Gsn-Related",,,,,,,C2751493,C537459,,,,
+BMGC_DS13378,BMG_DS044320,,"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT",,,,,DOID:0070028,APP-related cerebral amyloid angiopathy,C2751494,,104760;605714,MONDO:0017949,"ABeta amyloidosis, Arctic type",
+BMGC_DS13379,BMG_DS044321,,3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency,,,,,,,C2751532,C567784,605911,MONDO:0011614,3-hydroxy-3-methylglutaryl-CoA synthase deficiency,
+BMGC_DS13380,BMG_DS044322,,"Prostaglandin-Endoperoxide Synthase 1 Deficiency, Platelet",,,,,,,C2751535,C567786,605735,MONDO:0011588,platelet-type bleeding disorder 12,
+BMGC_DS13381,BMG_DS044323,,"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED",,,,,DOID:0070028,APP-related cerebral amyloid angiopathy,C2751536,,605714,MONDO:0011583,"cerebral amyloid angiopathy, APP-related",
+BMGC_DS13382,BMG_DS044324,,,,,,,,,C2751544,,605462,MONDO:0011556,"basal cell carcinoma, susceptibility to, 1",
+BMGC_DS13383,BMG_DS044325,,Neurodegeneration Due To Cerebral Folate Transport Deficiency,,,,,,,C2751584,C567791,613068,MONDO:0013110,neurodegenerative syndrome due to cerebral folate transport deficiency,
+BMGC_DS13384,BMG_DS044326,,,,,,,,,C2751593,,613067,MONDO:0013109,"leukemia, acute lymphocytic, susceptibility to, 2",
+BMGC_DS13385,BMG_DS044327,,,,,,,,,C2751595,,613065,MONDO:0013108,"leukemia, acute lymphocytic, susceptibility to, 1",
+BMGC_DS13386,BMG_DS044332,,,,,,,,,C2751603,,613060,MONDO:0013103,"epilepsy, idiopathic generalized, susceptibility to, 10",
+BMGC_DS13387,BMG_DS044335,,"Atrial Fibrillation, Familial, 8",,,,,,,C2751607,C567802,613055,MONDO:0013100,"atrial fibrillation, familial, 8",
+BMGC_DS13388,BMG_DS044336,,"Pituitary Hormone Deficiency, Combined, 1",,,,,,,C2751608,C567803,613038,MONDO:0024464,"pituitary hormone deficiency, combined, 1",
+BMGC_DS13389,BMG_DS044338,,Dursun Syndrome,,,,,,,C2751630,C567260,612541,MONDO:0012930,autosomal recessive severe congenital neutropenia due to G6PC3 deficiency,
+BMGC_DS13390,BMG_DS044343,,,,,,,,,C2751641,,613029,MONDO:0013093,glioma susceptibility 3,
+BMGC_DS13391,BMG_DS044344,,,,,,,,,C2751642,,613028,MONDO:0013092,glioma susceptibility 2,
+BMGC_DS13392,BMG_DS044345,,Glycogen Storage Disease IXC,,,,,DOID:0111043,glycogen storage disease IXc,C2751643,C567809,613027,MONDO:0013091,glycogen storage disease IXc,
+BMGC_DS13393,BMG_DS044348,,SCHIZOPHRENIA 13,,,,,DOID:0070089,schizophrenia 13,C2751663,,613025,MONDO:0013089,schizophrenia 13,
+BMGC_DS13394,BMG_DS044349,,,,,,,,,C2751665,,613024,MONDO:0013088,"follicular lymphoma, susceptibility to, 1",
+BMGC_DS13395,BMG_DS044350,,BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 2,,,,,DOID:0080527,bronchiectasis 2,C2751666,,600228;613021,MONDO:0013087,bronchiectasis with or without elevated sweat chloride 2,
+BMGC_DS13396,BMG_DS044354,,,,,,,,,C2751681,,613014,MONDO:0013083,"neuroblastoma, susceptibility to, 3",
+BMGC_DS13397,BMG_DS044355,,,,,,,,,C2751682,,613013,MONDO:0700041,"neuroblastoma, susceptibility to, 2",
+BMGC_DS13398,BMG_DS044357,,"Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1",,,,,,,C2751686,C567815,,,,
+BMGC_DS13399,BMG_DS044361,,Santos Syndrome,,,,,,,C2751698,C567819,613005,MONDO:0013077,Santos syndrome,
+BMGC_DS13400,BMG_DS044362,,,,,,,,,C2751729,,604827,MONDO:0011491,"epilepsy, idiopathic generalized, susceptibility to, 7",
+BMGC_DS13401,BMG_DS044363,,"Febrile Convulsions, Familial, 3a",,,,,,,C2751756,C567820,,MONDO:0800329,"febrile seizures, familial, 3a",
+BMGC_DS13402,BMG_DS044364,,"Retinitis Pigmentosa, Juvenile, Aipl1-Related",,,,,DOID:0110332,Leber congenital amaurosis 4,C2751763,C565778,,,,
+BMGC_DS13403,BMG_DS044365,,"Cone-Rod Dystrophy, Aipl1-Related",,,,,DOID:0110332,Leber congenital amaurosis 4,C2751764,C565778,,,,
+BMGC_DS13404,BMG_DS044366,,"Generalized Epilepsy With Febrile Seizures Plus, 7",,,,,DOID:0111295,generalized epilepsy with febrile seizures plus 7,C2751778,C567827,613863,MONDO:0013470,"generalized epilepsy with febrile seizures plus, type 7",
+BMGC_DS13405,BMG_DS044367,,"Retinitis Pigmentosa, Juvenile, SPATA7-Related",,,,,DOID:0110331,Leber congenital amaurosis 3,C2751780,C565814,,,,
+BMGC_DS13406,BMG_DS044368,,,,,,,,,C2751802,,613003,MONDO:0013076,"attention deficit-hyperactivity disorder, susceptibility to, 7",
+BMGC_DS13407,BMG_DS044369,,"IMMUNODEFICIENCY 83, SUSCEPTIBILITY TO VIRAL INFECTIONS",,,,,,,C2751803,,613002;603029,MONDO:0800187,"immunodeficiency 83, susceptibility to viral infections",
+BMGC_DS13408,BMG_DS044370,,"EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT",,,,,DOID:0070250,autosomal dominant Emery-Dreifuss muscular dystrophy 5,C2751805,,612999,MONDO:0013072,"Emery-Dreifuss muscular dystrophy 5, autosomal dominant",
+BMGC_DS13409,BMG_DS044371,,Emery-Dreifuss Muscular Dystrophy 4,,,,,,,C2751807,C567831,612998,MONDO:0013071,"Emery-Dreifuss muscular dystrophy 4, autosomal dominant",
+BMGC_DS13410,BMG_DS044372,,Spermatogenic Failure 7,,,,,DOID:0070173,spermatogenic failure 7,C2751811,C567832,612997,MONDO:0013070,spermatogenic failure 7,
+BMGC_DS13411,BMG_DS044373,,Optic Atrophy 7,,,,,DOID:0111437,optic atrophy 7,C2751812,C567833,612989,MONDO:0013069,"autosomal recessive optic atrophy, OPA7 type",
+BMGC_DS13412,BMG_DS044375,,"Cataract, Autosomal Recessive Congenital 3",,,,,,,C2751822,C567835,612968,MONDO:0013067,cataract 34 multiple types,
+BMGC_DS13413,BMG_DS044376,,"46, XY Disorders of Sex Development","Disorder of Sex Development, 46,XY",,,,,,C2751824,D058490,,MONDO:0020040,"46,XY disorder of sex development",
+BMGC_DS13414,BMG_DS044377,,Premature Ovarian Failure 7,,,,,,,C2751825,C567838,612964,MONDO:0013065,premature ovarian failure 7,
+BMGC_DS13415,BMG_DS044378,,Multiple Synostoses Syndrome 3,,,,,,,C2751826,C567839,612961,MONDO:0013064,multiple synostoses syndrome 3,
+BMGC_DS13416,BMG_DS044379,,"Ventricular Fibrillation, Paroxysmal Familial, 2",,,,,,,C2751829,C567841,612956,MONDO:0013063,"ventricular fibrillation, paroxysmal familial, 2",
+BMGC_DS13417,BMG_DS044380,,Long Qt Syndrome 12,,,,,DOID:0110653,long QT syndrome 12,C2751830,C567842,612955,MONDO:0013062,long QT syndrome 12,
+BMGC_DS13418,BMG_DS044381,,"Myopathy, Myofibrillar, Bag3-Related",,,,,,,C2751831,C567843,612954,MONDO:0013061,myofibrillar myopathy 6,
+BMGC_DS13419,BMG_DS044382,,"PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE",,,,,,,C2751842,,612953,MONDO:0013060,autosomal recessive Parkinson disease 14,
+BMGC_DS13420,BMG_DS044383,,"Leukoencephalopathy, Cystic, Without Megalencephaly",,,,,,,C2751843,C567845,612951,MONDO:0013058,cystic leukoencephalopathy without megalencephaly,
+BMGC_DS13421,BMG_DS044385,,"Hypomyelination, Global Cerebral",,,,,DOID:0080349,developmental and epileptic encephalopathy 39,C2751855,C567847,612949,MONDO:0013056,"developmental and epileptic encephalopathy, 39",
+BMGC_DS13422,BMG_DS044388,,Hadziselimovic Syndrome,,,,,,,C2751878,C567850,612946,MONDO:0013053,"microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type",
+BMGC_DS13423,BMG_DS044389,,"Ventricular Fibrillation, Paroxysmal Familial, 1",,,,,,,C2751898,C567851,603829,MONDO:0011376,"ventricular fibrillation, paroxysmal familial, type 1",
+BMGC_DS13424,BMG_DS044391,,RETINITIS PIGMENTOSA 42,,,,,,,C2751986,,612943;611119,MONDO:0013052,retinitis pigmentosa 42,
+BMGC_DS13425,BMG_DS044392,,"Cutis Laxa, Autosomal Recessive, Type IIB",,,,,,,C2751987,C567855,612940,MONDO:0013051,autosomal recessive cutis laxa type 2B,
+BMGC_DS13426,BMG_DS044393,,,,,,,,,C2752001,,612938,MONDO:0013050,"lethal polymalformative syndrome, Boissel type",
+BMGC_DS13427,BMG_DS044394,,"Congenital Disorder of Glycosylation, Type Io",,,,,,,C2752007,C567857,612937,MONDO:0013049,DPM3-congenital disorder of glycosylation,
+BMGC_DS13428,BMG_DS044395,,"Spastic Paraplegia-50, Autosomal Recessive",,,,,,,C2752008,C567858,612936,MONDO:0013048,hereditary spastic paraplegia 50,
+BMGC_DS13429,BMG_DS044396,,Glycogen Storage Disease XIV,,,,,,,C2752015,C567859,614921,MONDO:0013968,PGM1-congenital disorder of glycosylation,
+BMGC_DS13430,BMG_DS044397,,Glycogen Storage Disease XIII,,,,,,,C2752027,C567861,612932,MONDO:0013046,glycogen storage disease due to muscle beta-enolase deficiency,
+BMGC_DS13431,BMG_DS044399,,,,,,,,,C2752036,,612926,MONDO:0013044,atypical hemolytic-uremic syndrome with thrombomodulin anomaly,
+BMGC_DS13432,BMG_DS044400,,,,,,,,,C2752037,,612925,MONDO:0013043,atypical hemolytic-uremic syndrome with C3 anomaly,
+BMGC_DS13433,BMG_DS044401,,,,,,,,,C2752038,,612924,MONDO:0013042,atypical hemolytic-uremic syndrome with B factor anomaly,
+BMGC_DS13434,BMG_DS044402,,,,,,,,,C2752039,,612923,MONDO:0013041,atypical hemolytic-uremic syndrome with I factor anomaly,
+BMGC_DS13435,BMG_DS044403,,,,,,,,,C2752040,,612922,MONDO:0013040,atypical hemolytic-uremic syndrome with MCP/CD46 anomaly,
+BMGC_DS13436,BMG_DS044404,,Three M Syndrome 2,,,,,,,C2752041,C567862,612921,MONDO:0013039,3M syndrome 2,
+BMGC_DS13437,BMG_DS044405,,"Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi",,,,,,,C2752042,C567863,612918,MONDO:0013038,CLOVES syndrome,
+BMGC_DS13438,BMG_DS044406,,Giacheti Syndrome,,,,,,,C2752043,C567864,612917,MONDO:0013037,Giacheti syndrome,
+BMGC_DS13439,BMG_DS044407,,Zechi-Ceide Syndrome,,,,,,,C2752047,C567865,612916,MONDO:0013036,Zechi-Ceide syndrome,
+BMGC_DS13440,BMG_DS044408,,Orofaciodigital syndrome 11,,,,,DOID:0060381,orofaciodigital syndrome XI,C2752048,C557821,612913,MONDO:0013035,orofaciodigital syndrome XI,
+BMGC_DS13441,BMG_DS044410,,"Cerebral Palsy, Spastic Quadriplegic, 2",,,,,,,C2752061,C567867,612900,MONDO:0013033,"cerebral palsy, spastic quadriplegic, 2",
+BMGC_DS13442,BMG_DS044411,,,,,,,,,C2752062,,612899,MONDO:0013032,"epilepsy, idiopathic generalized, susceptibility to, 8",
+BMGC_DS13443,BMG_DS044412,,"Heterotopia, Periventricular, Associated With Chromosome 5q Deletion",,,,,,,C2752071,C567876,612881,MONDO:0013031,"chromosome 5Q14.3 deletion syndrome, distal",
+BMGC_DS13444,BMG_DS044413,,"Cardiomyopathy, Dilated, 1BB",,,,,,,C2752072,C567877,612877,MONDO:0013030,dilated cardiomyopathy 1BB,
+BMGC_DS13445,BMG_DS044414,,Erythrocyte Amp Deaminase Deficiency,,,,,,,C2752073,C567878,,,,
+BMGC_DS13446,BMG_DS044415,,ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY,,,,,DOID:0081326,oxoglutarate dehydrogenase deficiency,C2752074,,203740,MONDO:0008759,oxoglutaricaciduria,
+BMGC_DS13447,BMG_DS044416,,ALPHA-2-PLASMIN INHIBITOR DEFICIENCY,,,,,,,C2752081,,262850;613168,MONDO:0009883,alpha-2-plasmin inhibitor deficiency,
+BMGC_DS13448,BMG_DS044417,,"Neuropathy, Hereditary Sensory And Autonomic, Type IIA",,,,,,,C2752089,C567738,201300,MONDO:0024309,"neuropathy, hereditary sensory and autonomic, type 2A",
+BMGC_DS13449,BMG_DS044418,,,,,,,,,C2752090,,176780,MONDO:0008313,"pelvic organ prolapse, susceptibility to",
+BMGC_DS13450,BMG_DS044419,,"XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C",,,,,,,C2752147,,613208;278720,MONDO:0010211,xeroderma pigmentosum group C,
+BMGC_DS13451,BMG_DS044420,,,,,,,,,C2752149,,154230,MONDO:0007938,"46,XY sex reversal 4",
+BMGC_DS13452,BMG_DS044421,,,,,,,,,C2752157,,189490,MONDO:0008581,malposition of teeth with or without hypodontia/oligodontia,
+BMGC_DS13453,BMG_DS044423,,,,,,,DOID:0081092,acute myeloid leukemia with myelodysplasia-related changes,C2825139,,,,,
+BMGC_DS13454,BMG_DS044424,,,,,,,,,C2825149,,,MONDO:0850271,myeloid leukemia associated with down syndrome,
+BMGC_DS13455,BMG_DS044428,,,,,,,,,C2826048,,,MONDO:0035642,mixed phenotype acute leukemia with t(v;11q23.3),
+BMGC_DS13456,BMG_DS044429,,,,,,,DOID:0081080,acute myeloid leukemia with t(6;9) (p23;q34.1),C2826169,,,,,
+BMGC_DS13457,BMG_DS044430,,,,,,,DOID:0081083,acute myeloid leukemia with inv(3) (q21.3;q26.2) or t(3;3) (q21.3;q26.2),C2826172,,,MONDO:0018435,acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2),
+BMGC_DS13458,BMG_DS044431,,,,,,,DOID:0081089,acute myeloid leukemia with mutated NPM1,C2826177,,,MONDO:0044923,acute myeloid leukemia with mutated NPM1,
+BMGC_DS13459,BMG_DS044439,,"SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE",,,,,,,C2828721,,609471;614409,MONDO:0013737,hereditary spastic paraplegia 46,
+BMGC_DS13460,BMG_DS044440,,"DEAFNESS, AUTOSOMAL RECESSIVE 86",,,,,,,C2829265,,613577;614617,MONDO:0013826,autosomal recessive nonsyndromic hearing loss 86,
+BMGC_DS13461,BMG_DS044441,,"DEAFNESS, AUTOSOMAL RECESSIVE 88",,,,,,,C2829267,,615429;615427,MONDO:0014182,autosomal recessive nonsyndromic hearing loss 88,
+BMGC_DS13462,BMG_DS044476,,Infection due to Opisthorchis (felineus)(viverrini),,1F84,Opisthorchiasis,B66.0,,,C2830279,,,,,
+BMGC_DS13463,BMG_DS044477,,Infection due to cat liver fluke,,1F84,Opisthorchiasis,B66.0,,,C2830280,,,,,
+BMGC_DS13464,BMG_DS044573,,Adenomatosis of colon,,2E92.4Z,"Benign neoplasm of the large intestine, unspecified",D12.6,DOID:0080410,familial adenomatous polyposis 2,C2865399,,,,,
+BMGC_DS13465,BMG_DS044592,,Other aplastic anemias and other bone marrow failure syndromes,,,,D61,,,C2873777,,,,,
+BMGC_DS13466,BMG_DS044606,,Bernard-Soulier [giant platelet] syndrome,,3B62.Z,"Qualitative platelet defects, unspecified",D69.1,DOID:0111051,platelet-type bleeding disorder 18,C2873804,,,,,
+BMGC_DS13467,BMG_DS044607,,Thromboasthenia (hemorrhagic) (hereditary),,3B62.Z,"Qualitative platelet defects, unspecified",D69.1,DOID:0111051,platelet-type bleeding disorder 18,C2873805,,,,,
+BMGC_DS13468,BMG_DS044610,,Cell membrane receptor complex [CR3] defect,,,,D71,,,C2873813,,,,,
+BMGC_DS13469,BMG_DS044616,,Other and unspecified diseases of blood and blood-forming organs,,,,D75,,,C2873822,,,,,
+BMGC_DS13470,BMG_DS044617,,Polycythemia due to erythropoietin,,3A81.Z,"Acquired polycythaemia, unspecified",D75.1,DOID:0060474,familial erythrocytosis 2,C2873823,,,,,
+BMGC_DS13471,BMG_DS044618,,Polycythemia due to stress,,3A81.Z,"Acquired polycythaemia, unspecified",D75.1,DOID:0060474,familial erythrocytosis 2,C2873824,,,,,
+BMGC_DS13472,BMG_DS044627,,C1 esterase inhibitor [C1-INH] deficiency,,4A00.1Z,"Defects in the complement system, unspecified",D84.1,DOID:0060303;DOID:0060302;DOID:0060295;DOID:0060301;DOID:0060298,complement component 2 deficiency | complement component 4b deficiency | complement component 9 deficiency | type I complement component 8 deficiency | type II complement component 8 deficiency,C2873848,,,,,
+BMGC_DS13473,BMG_DS044770,1217051009,Isolated pituitary hormone deficiency,,,,,,,C2874188,,,,,Isolated deficiency of pituitary hormone | Isolated deficiency of pituitary hormone (disorder) | Isolated pituitary hormone deficiency
+BMGC_DS13474,BMG_DS044771,,Pituitary short stature,,5A61.0,Hypopituitarism,E23.0,DOID:0090072;DOID:0090087;DOID:0060875;DOID:0090073;DOID:0090076;DOID:0090092;DOID:0060873;DOID:0090080;DOID:0090075;DOID:0090077;DOID:0090071;DOID:0090082;DOID:0090084;DOID:0090074;DOID:0090093;DOID:0060874;DOID:0090078;DOID:0090070;DOID:0090085;DOID:0090094;DOID:0090086;DOID:0090083;DOID:0090081;DOID:0090079;DOID:0090089;DOID:0090090,hypogonadotropic hypogonadism 5 with or without anosmia | hypogonadotropic hypogonadism 7 with or without anosmia | hypogonadotropic hypogonadism 9 with or without anosmia | isolated growth hormone deficiency type IB | hypogonadotropic hypogonadism 21 with or without anosmia | hypogonadotropic hypogonadism 17 with or without anosmia | hypogonadotropic hypogonadism 6 with or without anosmia | isolated growth hormone deficiency type IA | isolated growth hormone deficiency type III | hypogonadotropic hypogonadism 10 with or without anosmia | hypogonadotropic hypogonadism 2 with or without anosmia | hypogonadotropic hypogonadism 22 with or without anosmia | hypogonadotropic hypogonadism 4 with or without anosmia | hypogonadotropic hypogonadism 1 with or without anosmia | hypogonadotropic hypogonadism 15 with or without anosmia | hypogonadotropic hypogonadism 16 with or without anosmia | hypogonadotropic hypogonadism 3 with or without anosmia | hypogonadotropic hypogonadism 14 with or without anosmia | hypogonadotropic hypogonadism 13 with or without anosmia | hypogonadotropic hypogonadism 19 with or without anosmia | hypogonadotropic hypogonadism 18 with or without anosmia | hypogonadotropic hypogonadism 12 with or without anosmia | hypogonadotropic hypogonadism | hypogonadotropic hypogonadism 11 with or without anosmia | hypogonadotropic hypogonadism 8 with or without anosmia | hypogonadotropic hypogonadism 20 with or without anosmia,C2874190,,,,,
+BMGC_DS13475,BMG_DS044780,,"DELAYED PUBERTY, SELF-LIMITED",,,,,,,C2874202,,606666;619613,MONDO:0859205,"delayed puberty, self-limited",
+BMGC_DS13476,BMG_DS044786,,Beriberi with cardiovascular manifestations,,,,E51.12,DOID:0070317,wet beriberi,C2874222,,,,,
+BMGC_DS13477,BMG_DS044787,,Shoshin disease,,,,E51.12,DOID:0070317,wet beriberi,C2874223,,,,,
+BMGC_DS13478,BMG_DS044823,,"GM2-GANGLIOSIDOSIS, ADULT",,,,,,,C2874270,,606869,,,
+BMGC_DS13479,BMG_DS044853,,Other and unspecified metabolic disorders,,,,E88,,,C2874310,,,,,
+BMGC_DS13480,BMG_DS044890,,Familial torsion dystonia,,8A02.0Z,"Primary dystonia, unspecified",G24.1,DOID:0090039;DOID:0090034;DOID:0060730;DOID:0090046;DOID:0090041;DOID:0090037;DOID:0090050;DOID:0090055;DOID:0090042;DOID:0090043;DOID:0090057;DOID:0090038,dystonia 27 | dystonia 21 | torsion dystonia 1 | dopa-responsive dystonia | torsion dystonia 2 | torsion dystonia 4 | torsion dystonia 13 | myoclonic dystonia 11 | dystonia 25 | X-linked dystonia-parkinsonism | torsion dystonia 6 | torsion dystonia 17,C2875058,,,,,
+BMGC_DS13481,BMG_DS044895,,Disseminated multiple sclerosis,,,,G35,,,C2875068,,,,,
+BMGC_DS13482,BMG_DS044936,,Epilepsies and epileptic syndromes undetermined as to whether they are focal or generalized,,8A6Z,"Epilepsy or seizures, unspecified",G40.8,DOID:0060281,photosensitive epilepsy,C2875129,,,,,
+BMGC_DS13483,BMG_DS045055,,Peroneal muscular atrophy (axonal type) (hypertrophic type),,8C20.Z,"Hereditary motor and sensory neuropathy, unspecified",G60.0,DOID:0110170;DOID:0110163;DOID:0110184;DOID:0110194;DOID:0110165;DOID:0110203;DOID:0110161;DOID:0110168;DOID:0110173;DOID:0110198;DOID:0110169;DOID:0110192;DOID:0110196;DOID:0110205;DOID:0110175;DOID:0110206;DOID:0110160;DOID:0110167;DOID:0110174;DOID:0110193;DOID:0110148;DOID:0110155;DOID:0110186;DOID:0110187;DOID:0110204;DOID:0110157;DOID:0110209;DOID:0110154;DOID:0110149;DOID:0110153;DOID:0110152;DOID:0110212;DOID:0110164;DOID:0110182;DOID:0090003;DOID:0110195;DOID:0110207;DOID:0110166;DOID:0110183;DOID:0110210;DOID:0110177,Charcot-Marie-Tooth disease type 2Y | Charcot-Marie-Tooth disease type 4F | Charcot-Marie-Tooth disease type 2J | Charcot-Marie-Tooth disease axonal type 2H | Charcot-Marie-Tooth disease type 2A1 | Charcot-Marie-Tooth disease type 1F | Charcot-Marie-Tooth disease type 2R | Charcot-Marie-Tooth disease recessive intermediate B | Charcot-Marie-Tooth disease X-linked dominant 6 | agenesis of the corpus callosum with peripheral neuropathy | Charcot-Marie-Tooth disease type 1A | Charcot-Marie-Tooth disease type 4J | Charcot-Marie-Tooth disease type 4D | Charcot-Marie-Tooth disease type 4E | Charcot-Marie-Tooth disease X-linked recessive 5 | Charcot-Marie-Tooth disease axonal type 2C | Charcot-Marie-Tooth disease axonal type 2T | Charcot-Marie-Tooth disease dominant intermediate F | Charcot-Marie-Tooth disease type 2D | Charcot-Marie-Tooth disease axonal type 2U | Charcot-Marie-Tooth disease type 4B3 | Charcot-Marie-Tooth disease type 2A2A | Charcot-Marie-Tooth disease axonal type 2O | Charcot-Marie-Tooth disease recessive intermediate D | Charcot-Marie-Tooth disease type 4G | Charcot-Marie-Tooth disease axonal type 2N | Charcot-Marie-Tooth disease axonal type 2F | Charcot-Marie-Tooth disease axonal type 2K | Charcot-Marie-Tooth disease type 4C | Charcot-Marie-Tooth disease axonal type 2Q | Charcot-Marie-Tooth disease axonal type 2L | Charcot-Marie-Tooth disease recessive intermediate C | Charcot-Marie-Tooth disease type 2E | Charcot-Marie-Tooth disease X-linked recessive 4 | Charcot-Marie-Tooth disease type 1B | Charcot-Marie-Tooth disease type 1E | Charcot-Marie-Tooth disease axonal type 2P | Charcot-Marie-Tooth disease X-linked dominant 1 | Charcot-Marie-Tooth disease dominant intermediate E | Charcot-Marie-Tooth disease type 4H | Charcot-Marie-Tooth disease type 4K,C2875300,,,,,
+BMGC_DS13484,BMG_DS045056,,Dominantly inherited sensory neuropathy,,8C4Z,"Disorders of nerve root, plexus or peripheral nerves, unspecified",G60.8,DOID:0070158;DOID:0070149;DOID:0070151,hereditary sensory and autonomic neuropathy type 6 | hereditary sensory and autonomic neuropathy type 7 | hereditary sensory neuropathy type 1E,C2875301,,,,,
+BMGC_DS13485,BMG_DS045057,,Nelaton's syndrome,,8C4Z,"Disorders of nerve root, plexus or peripheral nerves, unspecified",G60.8,DOID:0070158;DOID:0070149;DOID:0070151,hereditary sensory and autonomic neuropathy type 6 | hereditary sensory and autonomic neuropathy type 7 | hereditary sensory neuropathy type 1E,C2875302,,,,,
+BMGC_DS13486,BMG_DS045058,,Recessively inherited sensory neuropathy,,8C4Z,"Disorders of nerve root, plexus or peripheral nerves, unspecified",G60.8,DOID:0070158;DOID:0070149;DOID:0070151,hereditary sensory and autonomic neuropathy type 6 | hereditary sensory and autonomic neuropathy type 7 | hereditary sensory neuropathy type 1E,C2875303,,,,,
+BMGC_DS13487,BMG_DS045074,,Paraplegia (paraparesis) and quadriplegia (quadriparesis),,,,G82,,,C2875338,,,,,
+BMGC_DS13488,BMG_DS047090,,"Cardiac, heart or myocardial failure NOS",,BD1Z,"Heart failure, unspecified",I50.9,,,C2882277,,,,,
+BMGC_DS13489,BMG_DS047560,448421008,Sepsis caused by Streptococcus pneumoniae,,,,,,,C2887084,,,,,Sepsis caused by Streptococcus pneumoniae (disorder) | Sepsis caused by Streptococcus pneumoniae | Severe sepsis with acute organ dysfunction caused by Pneumococcus
+BMGC_DS13490,BMG_DS047563,448417001,Sepsis caused by Staphylococcus aureus,,,,,,,C2887088,,,,,Sepsis caused by Staphylococcus aureus (disorder) | Sepsis caused by Staphylococcus aureus
+BMGC_DS13491,BMG_DS047566,447685007,Sepsis caused by Haemophilus influenzae,,,,,,,C2887091,,,,,Sepsis caused by Haemophilus influenzae | Sepsis caused by Haemophilus influenzae (disorder) | Severe sepsis with acute organ dysfunction caused by Haemophilus influenzae
+BMGC_DS13492,BMG_DS047570,448813005,Sepsis due to Pseudomonas,,,,A41.52,,,C2887096,,,,,Sepsis caused by Pseudomonas | Sepsis caused by Pseudomonas (disorder) | Severe sepsis with acute organ dysfunction caused by Pseudomonas
+BMGC_DS13493,BMG_DS047571,449084002,Sepsis caused by Serratia,,,,,,,C2887097,,,,,Sepsis caused by Serratia (disorder) | Sepsis caused by Serratia | Severe sepsis with acute organ dysfunction caused by Serratia
+BMGC_DS13494,BMG_DS047776,,Bronchopneumonia due to S. pneumoniae,,,,J13,DOID:0040084,Streptococcus pneumonia,C2887412,,,,,
+BMGC_DS13495,BMG_DS047813,,"Respiratory Distress Syndrome, Acute",Respiratory Distress Syndrome,,,,,,C2887484,D012128,,MONDO:0006502,acute respiratory distress syndrome,
+BMGC_DS13496,BMG_DS047847,,Dental abscess with sinus,,DA09.61,Periapical abscess with sinus,K04.6,DOID:0060324,dental abscess,C2887541,,,,,
+BMGC_DS13497,BMG_DS047848,,Dentoalveolar abscess with sinus,,DA09.61,Periapical abscess with sinus,K04.6,DOID:0060324,dental abscess,C2887542,,,,,
+BMGC_DS13498,BMG_DS047959,,Crohn's disease [regional enteritis] of duodenum,,DD70.1,Crohn disease of small intestine,K50.0,DOID:0060191;DOID:0060188,gastroduodenal Crohn's disease | jejunoileitis,C2887749,,,,,
+BMGC_DS13499,BMG_DS047960,,Crohn's disease [regional enteritis] of ileum,,DD70.1,Crohn disease of small intestine,K50.0,DOID:0060191;DOID:0060188,gastroduodenal Crohn's disease | jejunoileitis,C2887750,,,,,
+BMGC_DS13500,BMG_DS047961,,Crohn's disease [regional enteritis] of jejunum,,DD70.1,Crohn disease of small intestine,K50.0,DOID:0060191;DOID:0060188,gastroduodenal Crohn's disease | jejunoileitis,C2887751,,,,,
+BMGC_DS13501,BMG_DS048230,,Psoriasiform diaper rash,,,,L22,,,C2888147,,,,,
+BMGC_DS13502,BMG_DS048235,,Other and unspecified dermatitis,,,,L30,,,C2888175,,,,,
+BMGC_DS13503,BMG_DS048236,,Von Zumbusch's disease,,EA90.40,Generalised pustular psoriasis,L40.1,DOID:0080474,pustular psoriasis 14,C2888177,,,,,
+BMGC_DS13504,BMG_DS048618,,Atrophie blanche (en plaque),,EF50,Livedoid vasculopathy,L95.0,DOID:0040099,livedoid vasculitis,C2888634,,,,,
+BMGC_DS13505,BMG_DS049585,699262001,Post traumatic osteoarthritis,,,,,,,C2894027,,,,,Post traumatic osteoarthritis | Post traumatic osteoarthritis (disorder)
+BMGC_DS13506,BMG_DS050995,,"Other and unspecified soft tissue disorders, not elsewhere classified",,,,M79,,,C2896437,,,,,
+BMGC_DS13507,BMG_DS051828,,Nephrotic syndrome with focal and segmental hyalinosis,,GB41,Nephrotic syndrome,N04.1,DOID:0111134;DOID:0111133;DOID:0111132;DOID:0111131;DOID:0111128,focal segmental glomerulosclerosis 1 | focal segmental glomerulosclerosis 7 | focal segmental glomerulosclerosis 8 | focal segmental glomerulosclerosis 6 | focal segmental glomerulosclerosis 9,C2902887,,,,,
+BMGC_DS13508,BMG_DS051829,,Nephrotic syndrome with focal and segmental sclerosis,,GB41,Nephrotic syndrome,N04.1,DOID:0111134;DOID:0111133;DOID:0111132;DOID:0111131;DOID:0111128,focal segmental glomerulosclerosis 1 | focal segmental glomerulosclerosis 7 | focal segmental glomerulosclerosis 8 | focal segmental glomerulosclerosis 6 | focal segmental glomerulosclerosis 9,C2902888,,,,,
+BMGC_DS13509,BMG_DS051830,,Nephrotic syndrome with focal glomerulonephritis,,GB41,Nephrotic syndrome,N04.1,DOID:0111134;DOID:0111133;DOID:0111132;DOID:0111131;DOID:0111128,focal segmental glomerulosclerosis 1 | focal segmental glomerulosclerosis 7 | focal segmental glomerulosclerosis 8 | focal segmental glomerulosclerosis 6 | focal segmental glomerulosclerosis 9,C2902889,,,,,
+BMGC_DS13510,BMG_DS051896,,Other and unspecified disorders of prostate,,,,N42,,,C2903013,,,,,
+BMGC_DS13511,BMG_DS052027,,,,,,,DOID:13576,twin-to-twin transfusion syndrome,C2909036,,,MONDO:0019805,twin to twin transfusion syndrome,
+BMGC_DS13512,BMG_DS052107,,Congenital cerebral aneurysm (nonruptured),,LA90.Z,"Structural developmental anomalies of the peripheral vascular system, unspecified",Q28.3,DOID:0060670;DOID:0060671,cerebral cavernous malformation 2 | cerebral cavernous malformation 3,C2910157,,,,,
+BMGC_DS13513,BMG_DS052120,,Hemimelia of limb NOS,,LD24.0Z,"Syndromes with micromelia, unspecified",Q73.8,DOID:0110962;DOID:0110967;DOID:0110975;DOID:0110963,brachydactyly-preaxial hallux varus syndrome | brachydactyly type B2 | brachydactyly type A4 | Ballard syndrome,C2910324,,,,,
+BMGC_DS13514,BMG_DS052121,,Asphyxiating thoracic dysplasia [Jeune],,LD24.BZ,"Short rib syndromes, unspecified",Q77.2,DOID:0110095;DOID:0110088;DOID:0110092;DOID:0110085;DOID:0050592;DOID:0110087;DOID:0110090;DOID:0110094;DOID:0110089;DOID:0110093,asphyxiating thoracic dystrophy 3 | asphyxiating thoracic dystrophy | short-rib thoracic dysplasia 8 with or without polydactyly | asphyxiating thoracic dystrophy 1 | asphyxiating thoracic dystrophy 4 | short-rib thoracic dysplasia 6 with or without polydactyly | asphyxiating thoracic dystrophy 5 | short-rib thoracic dysplasia 13 with or without polydactyly | short-rib thoracic dysplasia 11 with or without polydactyly | short-rib thoracic dysplasia 7 with or without polydactyly,C2910340,,,,,
+BMGC_DS13515,BMG_DS052123,,Inherited keratosis palmaris et plantaris,,LC7Z,"Structural developmental anomalies of the skin, unspecified",Q82.8,DOID:0070142;DOID:0070132;DOID:0070141;DOID:0070129;DOID:0070130;DOID:0070134;DOID:0070138;DOID:0070135;DOID:0070131;DOID:0070137;DOID:0070140;DOID:0070136;DOID:0070133,autosomal dominant cutis laxa | autosomal recessive cutis laxa type IIIB | autosomal recessive cutis laxa type IIA | autosomal recessive cutis laxa type IID | autosomal dominant cutis laxa 3 | autosomal recessive cutis laxa type IIIA | autosomal recessive cutis laxa type IB | autosomal dominant cutis laxa 2 | autosomal dominant cutis laxa 1 | autosomal recessive cutis laxa type IIB | autosomal recessive cutis laxa type IIC | autosomal recessive cutis laxa type II classic type | autosomal recessive cutis laxa type IA,C2910342,,,,,
+BMGC_DS13516,BMG_DS052124,,Keratosis follicularis [Darier-White],,LC7Z,"Structural developmental anomalies of the skin, unspecified",Q82.8,DOID:0070142;DOID:0070132;DOID:0070141;DOID:0070129;DOID:0070130;DOID:0070134;DOID:0070138;DOID:0070135;DOID:0070131;DOID:0070137;DOID:0070140;DOID:0070136;DOID:0070133,autosomal dominant cutis laxa | autosomal recessive cutis laxa type IIIB | autosomal recessive cutis laxa type IIA | autosomal recessive cutis laxa type IID | autosomal dominant cutis laxa 3 | autosomal recessive cutis laxa type IIIA | autosomal recessive cutis laxa type IB | autosomal dominant cutis laxa 2 | autosomal dominant cutis laxa 1 | autosomal recessive cutis laxa type IIB | autosomal recessive cutis laxa type IIC | autosomal recessive cutis laxa type II classic type | autosomal recessive cutis laxa type IA,C2910343,,,,,
+BMGC_DS13517,BMG_DS052131,,Trisomy 18 and Trisomy 13,,,,Q91,,,C2910353,,,,,
+BMGC_DS13518,BMG_DS052138,,"46, XY with streak gonads",,LD2A.Z;LD56.Z,"Malformative disorders of sex development, unspecified | Chimaera 46, XX, 46, XY, unspecified",Q56.1;Q99.1,DOID:0090091,hypogonadotropic hypogonadism 23 with or without anosmia,C2910379,,,,,
+BMGC_DS13519,BMG_DS052232,444976001,Congenital hemolytic uremic syndrome,,,,,,,C2919522,,,,,Congenital hemolytic uremic syndrome (disorder) | Congenital haemolytic uraemic syndrome | Congenital hemolytic uremic syndrome
+BMGC_DS13520,BMG_DS052236,,Nonsustained Ventricular Tachycardia,"Tachycardia, Ventricular",,,,,,C2919575,D017180,,,,
+BMGC_DS13521,BMG_DS052256,,,,,,,,,C2919692,,,MONDO:0018434,acute myeloid leukemia with t(9;11)(p22;q23),
+BMGC_DS13522,BMG_DS052268,7265005;444707001,Glycogen storage disease type Ia,,,,,,,C2919796,,232200,MONDO:0009287,glycogen storage disease due to glucose-6-phosphatase deficiency type IA,"Glycogen storage disease, type I | Hepatorenal glycogen storage disease | von Gierke's disease | GSD I | Liver glycogen disease | von Gierke disease | Glycogen storage disease, type I (disorder) | Glycogen storage disease, type 1 | Glycogen storage disease type Ia (disorder) | Glycogen storage disease type Ia"
+BMGC_DS13523,BMG_DS052277,64766004;444546002,Chronic ulcerative colitis,,,,,,,C2919828,,,,,Colitis gravis | Ulcerative colitis | Ulcerative colitis (disorder) | Idiopathic proctocolitis | UC - ulcerative colitis | Chronic ulcerative colitis (disorder) | Chronic ulcerative colitis
+BMGC_DS13524,BMG_DS052293,,,,,,,,,C2919945,,,MONDO:0000820,cerebral cavernous malformation,
+BMGC_DS13525,BMG_DS052318,,Bilateral Wilms Tumor,Wilms Tumor,,,,,,C2930471,D009396,,,,
+BMGC_DS13526,BMG_DS052322,,Pulmonary Fibrosis - from Asbestos Exposure,Asbestosis,,,,,,C2930617,D001195,,,,
+BMGC_DS13527,BMG_DS052323,,Sex Differentiation Disorders,Disorders of Sex Development,,,,,,C2930619,D012734,,MONDO:0002145,disorder of sexual differentiation,
+BMGC_DS13528,BMG_DS052327,,Familial acanthosis nigricans,,,,,,,C2930792,C531598,100600,MONDO:0043003,familial acanthosis nigricans,
+BMGC_DS13529,BMG_DS052330,,Primary visual agnosia,,,,,DOID:0060155,visual agnosia,C2930796,C531604,,,,
+BMGC_DS13530,BMG_DS052335,,Familial antiphospholipid syndrome,,,,,,,C2930802,C531622,107320,MONDO:8000014,familial antiphospholipid syndrome,
+BMGC_DS13531,BMG_DS052365,,Familial pityriasis rubra pilaris,,,,,,,C2930842,C531784,173200,MONDO:0008251,familial pityriasis rubra pilaris,
+BMGC_DS13532,BMG_DS052366,,Idiopathic intracranial hypertension with papilledema,,,,,,,C2930843,C531795,,,,
+BMGC_DS13533,BMG_DS052367,,Hypopituitarism and septooptic 'dysplasia',,,,,,,C2930844,C531815,,,,
+BMGC_DS13534,BMG_DS052378,,"Premature ovarian failure, familial",,,,,,,C2930861,C535272,,MONDO:0019852,inherited primary ovarian failure,
+BMGC_DS13535,BMG_DS052382,,Ramer Ladda syndrome,,,,,DOID:0060467,humeroradial synostosis,C2930865,C535284,143050,MONDO:0007737,humeroradial synostosis,
+BMGC_DS13536,BMG_DS052383,,Ramos Arroyo Clark syndrome,,,,,,,C2930866,C535286,122430,MONDO:0007382,Ramos-Arroyo syndrome,
+BMGC_DS13537,BMG_DS052394,,"Cataract, congenital, with microcornea or slight microphthalmia",,,,,,,C2930878,C535338,,,,
+BMGC_DS13538,BMG_DS052404,,"Congenital thrombotic disease, due to Protein C deficiency",,,,,,,C2930896,C535424,,,,
+BMGC_DS13539,BMG_DS052406,59026006,Benign essential blepharospasm,,,,,,,C2930898,C535428,,MONDO:0011728,benign essential blepharospasm,Blepharospasm | Blepharospasm (disorder) | Spasm of eyelids | Essential blepharospasm | Benign essential blepharospasm | Blepharospasm (spasm of eyelid)
+BMGC_DS13540,BMG_DS052408,,Beta-sarcoglycanopathy,,,,,,,C2930900,C535435,,MONDO:0016142,qualitative or quantitative defects of beta-sarcoglycan,
+BMGC_DS13541,BMG_DS052417,,Ring Chromosome 14 Syndrome,,,,,DOID:0070621,ring chromosome 14 syndrome,C2930916,C535487,616606,MONDO:0014708,ring chromosome 14,
+BMGC_DS13542,BMG_DS052427,,Abdominal obesity metabolic syndrome,,,,,DOID:0060611,abdominal obesity-metabolic syndrome,C2930930,C535554,,MONDO:0000816,abdominal obesity-metabolic syndrome,
+BMGC_DS13543,BMG_DS052448,,Freire-Maia odontotrichomelic syndrome,,,,,,,C2930960,C535637,273400,MONDO:0010111,odontotrichomelic syndrome,
+BMGC_DS13544,BMG_DS052449,,Frenkel Russe syndrome,,,,,,,C2930961,C535638,267900,MONDO:0009980,retinal telangiectasia and hypogammaglobulinemia,
+BMGC_DS13545,BMG_DS052455,,,,,,,,,C2930967,,,MONDO:0000386,"digestive system neuroendocrine tumor, grade 1/2",
+BMGC_DS13546,BMG_DS052458,389167007,Acromesomelic dysplasia Hunter-Thompson type,,,,,DOID:0080049,acromesomelic dysplasia,C2930970,C535658,201250,MONDO:0008717,"acromesomelic dysplasia 2C, Hunter-Thompson type",Hunter-Thompson dysplasia | Acromesomelic dysplasia Hunter-Thompson type (disorder) | Acromesomelic dysplasia Hunter-Thompson type
+BMGC_DS13547,BMG_DS052462,,Acute erythroleukemia,,,,,,,C2930974,C535673,,,,
+BMGC_DS13548,BMG_DS052463,,Acute erythroleukemia - M6a subtype,,,,,,,C2930975,C535673,,,,
+BMGC_DS13549,BMG_DS052464,,Acute myeloid leukemia FAB-M6,,,,,,,C2930976,C535673,,,,
+BMGC_DS13550,BMG_DS052465,,Acute erythroleukemia - M6b subtype,,,,,,,C2930977,C535673,,,,
+BMGC_DS13551,BMG_DS052466,,Richieri Costa Da Silva syndrome,,,,,,,C2930978,C535675,255710,MONDO:0009716,Richieri Costa-da Silva syndrome,
+BMGC_DS13552,BMG_DS052468,,,,,,,,,C2930980,,145600,MONDO:0007783,"malignant hyperthermia, susceptibility to, 1",
+BMGC_DS13553,BMG_DS052469,,,,,,,,,C2930981,,154275,MONDO:0007939,"malignant hyperthermia, susceptibility to, 2",
+BMGC_DS13554,BMG_DS052470,,,,,,,,,C2930982,,154276,MONDO:0007940,"malignant hyperthermia, susceptibility to, 3",
+BMGC_DS13555,BMG_DS052472,,"Maple syrup urine disease, type 1A",,,,,,,C2930989,C535710,,,,
+BMGC_DS13556,BMG_DS052473,,"Maple syrup urine disease, type 1B",,,,,,,C2930990,C535711,620698,MONDO:0023692,maple syrup urine disease type 1B,
+BMGC_DS13557,BMG_DS052476,,Familial duodenal atresia,,,,,DOID:0080216,duodenal atresia,C2930994,C535720,,,,
+BMGC_DS13558,BMG_DS052477,,Dyschromatosis universalis hereditaria,,,,,DOID:0060304,dyschromatosis universalis hereditaria,C2930995,C535730,,MONDO:0000736,dyschromatosis universalis hereditaria,
+BMGC_DS13559,BMG_DS052479,,Congenital disorder of glycosylation type 1C,,,,,,,C2930997,C535741,603147,MONDO:0011291,ALG6-congenital disorder of glycosylation 1C,
+BMGC_DS13560,BMG_DS052480,711155008,Congenital disorder of glycosylation type 1G,,,,,,,C2931001,C535745,607143,MONDO:0011783,ALG12-congenital disorder of glycosylation,ALG12-congenital disorder of glycosylation (disorder) | ALG12-congenital disorder of glycosylation | Congenital disorder of glycosylation type Ig | Congenital disorder of glycosylation type 1G
+BMGC_DS13561,BMG_DS052481,,Congenital disorder of glycosylation type 1H,,,,,,,C2931002,C535746,608104,MONDO:0011969,ALG8-congenital disorder of glycosylation,
+BMGC_DS13562,BMG_DS052482,,Congenital disorder of glycosylation type 1J,,,,,,,C2931004,C535748,608093,MONDO:0011964,DPAGT1-congenital disorder of glycosylation,
+BMGC_DS13563,BMG_DS052483,720941007,Congenital disorder of glycosylation type 1K,,,,,,,C2931005,C535749,608540,MONDO:0012052,ALG1-congenital disorder of glycosylation,Asparagine-linked glycosylation 1 congenital disorder of glycosylation (disorder) | Asparagine-linked glycosylation 1 congenital disorder of glycosylation | ALG1 congenital disorder of glycosylation | Congenital disorder of glycosylation type 1K | Carbohydrate deficient glycoprotein syndrome type Ik | Mannosyltransferase 1 deficiency | ALG1-CDG - asparagine-linked glycosylation 1 congenital disorder of glycosylation
+BMGC_DS13564,BMG_DS052484,720978005,Congenital disorder of glycosylation type 1L,,,,,,,C2931006,C535750,608776,MONDO:0012117,ALG9-congenital disorder of glycosylation,Asparagine-linked glycosylation 9 congenital disorder of glycosylation (disorder) | Asparagine-linked glycosylation 9 congenital disorder of glycosylation | ALG9 congenital disorder of glycosylation | Carbohydrate deficient glycoprotein syndrome type IL | Congenital disorder of glycosylation type 1L | Congenital disorder of glycosylation type IL | Mannosyltransferase 7-9 deficiency | ALG9-CDG - asparagine-linked glycosylation 9 congenital disorder of glycosylation
+BMGC_DS13565,BMG_DS052485,,Congenital disorder of glycosylation type 1X,,,,,,,C2931007,C535751,615597,MONDO:0014271,STT3B-congenital disorder of glycosylation,
+BMGC_DS13566,BMG_DS052486,,Congenital disorder of glycosylation type 2A,,,,,DOID:0070253,congenital disorder of glycosylation type IIa,C2931008,C535752,212066,MONDO:0008908,MGAT2-congenital disorder of glycosylation,
+BMGC_DS13567,BMG_DS052487,,Congenital disorder of glycosylation type 2D,,,,,DOID:0070256,congenital disorder of glycosylation type IId,C2931009,C535753,607091,MONDO:0011772,B4GALT1-congenital disorder of glycosylation,
+BMGC_DS13568,BMG_DS052488,,Congenital disorder of glycosylation type 2E,,,,,DOID:0070257,congenital disorder of glycosylation type IIe,C2931010,C535754,608779,MONDO:0012118,COG7-congenital disorder of glycosylation,
+BMGC_DS13569,BMG_DS052489,,"Congenital disorder of glycosylation, type 2G",,,,,DOID:0070259,congenital disorder of glycosylation type IIg,C2931011,C535756,611209,MONDO:0012637,COG1-congenital disorder of glycosylation,
+BMGC_DS13570,BMG_DS052491,,"Cystinosis, benign, nonnephropathic",,,,,,,C2931013,C535765,219750,MONDO:0009064,ocular cystinosis,
+BMGC_DS13571,BMG_DS052496,,,,,,,,,C2931019,,183600,MONDO:0008464,split hand-foot malformation 1,
+BMGC_DS13572,BMG_DS052505,,"Nevi flammei, familial multiple",,,,,DOID:0111529,familial multiple nevi flammei,C2931029,C535816,163000,MONDO:0008094,familial multiple nevi flammei,
+BMGC_DS13573,BMG_DS052511,,"Pulmonary alveolar proteinosis, congenital",,,,,,,C2931035,C535832,,,,
+BMGC_DS13574,BMG_DS052513,,"Pancreatic cancer, adult",,,,,,,C2931037,C535836,,,,
+BMGC_DS13575,BMG_DS052514,,,,,,,,,C2931038,,260350,MONDO:0015278,familial pancreatic carcinoma,
+BMGC_DS13576,BMG_DS052517,403001;297227008;414380008,Hawkinsinuria,,,,,DOID:0111362,hawkinsinuria,C2931042,C535845,140350,MONDO:0007700,hawkinsinuria,4-Hydroxyphenylpyruvate dioxygenase deficiency | Hawkinsinuria | 4-Hydroxyphenylpyruvate hydroxylase deficiency | Tyrosinaemia type III | Tyrosinemia type III | 4-Hydroxyphenylpyruvate dioxygenase deficiency (disorder) | Hawkinsinuria | Hawkinsinuria (disorder) | Hawkinsinuria (disorder) | Hawkinsinuria | HPD-gene related hawkinsinuria
+BMGC_DS13577,BMG_DS052519,,"Heart defect, tongue hamartoma and polysyndactyly",,,,,DOID:0111591,"congenital heart defects, hamartomas of tongue, and polysyndactyly",C2931046,C535849,,,,
+BMGC_DS13578,BMG_DS052521,,HEM dysplasia,,,,,DOID:0111588,Greenberg dysplasia,C2931048,C535858,215140,MONDO:0008974,Greenberg dysplasia,
+BMGC_DS13579,BMG_DS052525,,Rubinstein Taybi like syndrome,,,,,,,C2931052,C535877,180850,MONDO:0043195,Rubinstein Taybi like syndrome,
+BMGC_DS13580,BMG_DS052526,722493007,Rudd Klimek syndrome,,,,,,,C2931053,C535879,600145,MONDO:0010831,familial caudal dysgenesis,Familial caudal dysgenesis (disorder) | Familial caudal dysgenesis | Rudd Klimek syndrome
+BMGC_DS13581,BMG_DS052531,,Marfan Syndrome Type 2,Marfan Syndrome,,,,,,C2931058,D008382,,,,
+BMGC_DS13582,BMG_DS052532,254234005,Marie Unna congenital hypotrichosis,,,,,,,C2931059,C535912,,MONDO:0018631,Marie Unna hereditary hypotrichosis,Marie Unna syndrome | Marie Unna syndrome (disorder) | Marie Unna hereditary hypotrichosis | Marie Unna congenital hypotrichosis
+BMGC_DS13583,BMG_DS052533,733095006,Mononen Karnes Senac syndrome,,,,,DOID:0110973,Mononen-Karnes-Senac syndrome,C2931060,C535914,,,,Mononen Karnes Senac syndrome | Skeletal dysplasia brachydactyly syndrome | Skeletal dysplasia brachydactyly syndrome (disorder)
+BMGC_DS13584,BMG_DS052537,,Pierre Robin Sequence with Facial and Digital Anomalies,,,,,,,C2931064,C564078,311895,MONDO:0010710,Pierre Robin syndrome-faciodigital anomaly syndrome,
+BMGC_DS13585,BMG_DS052540,,"Cholestasis, progressive familial intrahepatic 4",,,,,,,C2931067,C535442,615878,MONDO:0014381,"cholestasis, progressive familial intrahepatic, 4",
+BMGC_DS13586,BMG_DS052544,,Epidermolysa bullosa simplex and limb girdle muscular dystrophy,,,,,,,C2931072,C535955,226670,MONDO:0009181,"epidermolysis bullosa simplex 5B, with muscular dystrophy",
+BMGC_DS13587,BMG_DS052545,,"Collagenopathy, type 2 alpha 1",,,,,,,C2931073,C535964,,MONDO:0022800,type 2 collagenopathy,
+BMGC_DS13588,BMG_DS052553,,Familial apoceruloplasmin deficiency,,,,,,,C2931082,C536004,,,,
+BMGC_DS13589,BMG_DS052562,,Maternally Inherited Leigh Syndrome,,,,,,,C2931092,C536035,,MONDO:0016814,maternally-inherited Leigh syndrome,
+BMGC_DS13590,BMG_DS052563,,"Osteogenesis Imperfecta, Type V",,,,,,,C2931093,C567042,610967,MONDO:0012591,osteogenesis imperfecta type 5,
+BMGC_DS13591,BMG_DS052570,721232000,Hydrolethalus syndrome,,,,,DOID:0050779,hydrolethalus syndrome,C2931104,C536079,,MONDO:0006037,hydrolethalus syndrome,Hydrolethalus syndrome (disorder) | Hydrolethalus syndrome
+BMGC_DS13592,BMG_DS052571,,"Hypercalciuria, childhood idiopathic",,,,,,,C2931105,C536082,,,,
+BMGC_DS13593,BMG_DS052573,,"Myasthenic syndrome, congenital, postsynaptic slow-channel",,,,,,,C2931107,C536091,601462,MONDO:0011088,congenital myasthenic syndrome 1A,
+BMGC_DS13594,BMG_DS052577,,"Myopia, susceptibility to",,,,,,,C2931111,C536105,,,,
+BMGC_DS13595,BMG_DS052578,,,,,,,DOID:0111072,myostatin-related muscle hypertrophy,C2931112,,614160,MONDO:0013598,myostatin-related muscle hypertrophy,
+BMGC_DS13596,BMG_DS052582,,Cerebral Nocardiosis,Nocardia Infections,,,,,,C2931116,D009617,,,,
+BMGC_DS13597,BMG_DS052583,,Fetal megacystis,,,,,,,C2931117,C536139,,,,
+BMGC_DS13598,BMG_DS052584,,Megalocytic interstitial nephritis,,,,,,,C2931118,C536144,,,,
+BMGC_DS13599,BMG_DS052587,,Meier Blumberg Imahorn syndrome,,,,,DOID:0060881,renal hypomagnesemia 5 with ocular involvement,C2931121,C536148,,,,
+BMGC_DS13600,BMG_DS052588,,Keratosis palmoplantaris striata 1,,,,,DOID:0081108,keratosis palmoplantaris striata 1,C2931122,C536162,148700,MONDO:0007859,"palmoplantar keratoderma i, striate, focal, or diffuse",
+BMGC_DS13601,BMG_DS052589,,Keratosis palmoplantaris striata 3,,,,,DOID:0081110,keratosis palmoplantaris striata 3,C2931123,C536163,607654,MONDO:0011881,keratosis palmoplantaris striata 3,
+BMGC_DS13602,BMG_DS052596,,Clark-Baraitser syndrome,,,,,DOID:0080234,Clark-Baraitser syndrome,C2931130,C536208,617752;300602,MONDO:0030914,Clark-Baraitser syndrome,
+BMGC_DS13603,BMG_DS052597,,"Crigler Najjar syndrome, type 2",,,,,,,C2931132,C536213,606785,MONDO:0011725,Crigler-Najjar syndrome type 2,
+BMGC_DS13604,BMG_DS052598,,Pediatric Crohn's disease,,,,,,,C2931133,C536215,,,,
+BMGC_DS13605,BMG_DS052599,,"Cutis laxa, recessive",,,,,,,C2931134,C536225,,,,
+BMGC_DS13606,BMG_DS052600,,Blepharophimosis syndrome type 1,,,,,,,C2931135,C536233,,,,
+BMGC_DS13607,BMG_DS052601,,Blepharophimosis syndrome type 2,,,,,,,C2931136,C536234,,,,
+BMGC_DS13608,BMG_DS052605,,Nonkeratan-sulfate-excreting Morquio syndrome,,,,,,,C2931140,C536247,252300,MONDO:0009647,Morquio syndrome C,
+BMGC_DS13609,BMG_DS052607,721887007,Qazi Markouizos syndrome,,,,,DOID:0050740,Qazi Markouizos syndrome,C2931142,C536259,600096,MONDO:0010816,Qazi Markouizos syndrome,Puerto Rican infant hypotonia syndrome (disorder) | Dysharmonic skeletal maturation and muscular fiber disproportion syndrome | Dysharmonic skeletal maturation and muscular fibre disproportion syndrome | Puerto Rican infant hypotonia syndrome | Qazi Markouizos syndrome
+BMGC_DS13610,BMG_DS052611,,Radio renal syndrome,,,,,,,C2931146,C536267,179280,MONDO:0008359,radio-renal syndrome,
+BMGC_DS13611,BMG_DS052618,,Immunoglobulin a deficiency 1,,,,,,,C2931161,C536290,137100,MONDO:0007644,IgAD1,
+BMGC_DS13612,BMG_DS052626,,Juvenile pauciarticular chronic arthritis,,,,,,,C2931171,C536312,,MONDO:0019433,oligoarticular juvenile idiopathic arthritis,
+BMGC_DS13613,BMG_DS052630,,"Vestibulocochlear Dysfunction, Progressive",,,,,,,C2931176,C536346,193005,MONDO:0008655,"vestibulocochlear dysfunction, progressive",
+BMGC_DS13614,BMG_DS052633,,Angiofollicular ganglionic hyperplasia,,,,,DOID:0111157,Castleman disease,C2931179,C536362,,,,
+BMGC_DS13615,BMG_DS052634,,Abdominal angiostrongyliasis,,,,,DOID:0050256,angiostrongyliasis,C2931180,C536369,,,,
+BMGC_DS13616,BMG_DS052635,,Intravitreal angiostrongyliasis,,,,,DOID:0050256,angiostrongyliasis,C2931181,C536369,,,,
+BMGC_DS13617,BMG_DS052641,62332007,Nephropathic cystinosis,,,,,DOID:1064,cystinosis,C2931187,,219800,MONDO:0100151,nephropathic cystinosis,Infantile nephropathic cystinosis | Nephropathic cystinosis | Lignac-Fanconi syndrome | Infantile nephropathic cystinosis (disorder)
+BMGC_DS13618,BMG_DS052645,,Prinzmetal's variant angina,,,,,,,C2931193,C536421,,,,
+BMGC_DS13619,BMG_DS052651,,,,,,,DOID:5958,bladder urachal carcinoma,C2931202,,,MONDO:0003715,bladder urachal carcinoma,
+BMGC_DS13620,BMG_DS052653,,"Usher syndrome, type 1B",,,,,,,C2931206,C536485,276900,MONDO:0700087,Usher syndrome type 1B,
+BMGC_DS13621,BMG_DS052654,,"Usher syndrome, type 1C",,,,,,,C2931207,C536486,,,,
+BMGC_DS13622,BMG_DS052655,,"Usher syndrome, type 1D",,,,,,,C2931208,C536487,,,,
+BMGC_DS13623,BMG_DS052657,,"Usher syndrome, type 1F",,,,,,,C2931210,C536489,,,,
+BMGC_DS13624,BMG_DS052659,,"Usher syndrome, type 2C",,,,,,,C2931213,C536492,605472,MONDO:0011558,Usher syndrome type 2C,
+BMGC_DS13625,BMG_DS052660,,Tetra amelia with ectodermal dysplasia and lacrimal duct abnormalities,,,,,,,C2931214,C536496,273390,MONDO:0010109,tetraamelia with ectodermal dysplasia and lacrimal duct abnormalities,
+BMGC_DS13626,BMG_DS052664,,Tetraamelia multiple malformations,,,,,,,C2931218,C536500,,MONDO:0010110,tetraamelia-multiple malformations syndrome,
+BMGC_DS13627,BMG_DS052669,,6 alpha mercaptopurine sensitivity,,,,,DOID:0080172,poor metabolism of thiopurines,C2931223,C536512,,MONDO:0000210,thiopurine metabolic disease,
+BMGC_DS13628,BMG_DS052674,,"VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS",,,,,DOID:0111766,X-linked VACTERL association,C2931228,,314390,MONDO:0010752,"VACTERL association, X-linked, with or without hydrocephalus",
+BMGC_DS13629,BMG_DS052675,,Vacuolar myopathy,,,,,,,C2931230,C536522,609500;MTHU045596,MONDO:0012286,"myopathy, autophagic vacuolar, infantile-onset",
+BMGC_DS13630,BMG_DS052682,,,,,,,,,C2931238,,190600,MONDO:0008605,"triphalangeal thumb, Nonopposable",
+BMGC_DS13631,BMG_DS052685,,Waldmann disease,,,,,,,C2931241,C536567,152800,MONDO:0007916,primary intestinal lymphangiectasia,
+BMGC_DS13632,BMG_DS052688,,"Craniometaphyseal dysplasia, autosomal recessive type",,,,,,,C2931244,C536570,218400,MONDO:0009035,"craniometaphyseal dysplasia, autosomal recessive",
+BMGC_DS13633,BMG_DS052689,,Bone Marrow Failure Disorders,Bone Marrow Failure Disorders,,,,,,C2931245,D000080983,,MONDO:0000159,bone marrow failure syndrome,
+BMGC_DS13634,BMG_DS052690,,Potocki-Lupski syndrome,,,,,DOID:0060853,Potocki-Lupski syndrome,C2931246,C538355,610883,MONDO:0012574,Potocki-Lupski syndrome,
+BMGC_DS13635,BMG_DS052691,,"Chromosome 18, monosomy 18Q",,,,,DOID:0060407,chromosome 18q deletion syndrome,C2931249,C536580,,,,
+BMGC_DS13636,BMG_DS052695,,"Alport syndrome, dominant type",,,,,,,C2931253,C536586,,,,
+BMGC_DS13637,BMG_DS052696,,"Alport syndrome, recessive type",,,,,,,C2931254,C536587,,,,
+BMGC_DS13638,BMG_DS052699,,"Amaurosis congenita of Leber, type 1",,,,,,,C2931258,C536600,204000,MONDO:0008764,Leber congenital amaurosis 1,
+BMGC_DS13639,BMG_DS052701,,,,,,,,,C2931263,,,MONDO:0031037,famililal cerebral cavernous malformations,
+BMGC_DS13640,BMG_DS052704,,Scapuloperoneal myopathy,,,,,DOID:0060253,scapuloperoneal myopathy,C2931268,C536624,,MONDO:0000727,scapuloperoneal myopathy,
+BMGC_DS13641,BMG_DS052711,,Spastic paraplegia 17,,,,,,,C2931276,C536644,270685,MONDO:0010043,hereditary spastic paraplegia 17,
+BMGC_DS13642,BMG_DS052714,716191002,Perniola Krajewska Carnevale syndrome,,,,,,,C2931280,C536660,,MONDO:0008756,alopecia - intellectual disability syndrome,Alopecia and intellectual disability syndrome (disorder) | Alopecia and intellectual disability syndrome | Perniola Krajewska Carnevale syndrome
+BMGC_DS13643,BMG_DS052722,,"Welander distal myopathy, Swedish type",,,,,,,C2931290,C536690,,,,
+BMGC_DS13644,BMG_DS052723,715504003,Wells Jankovic syndrome,,,,,DOID:0081100,spastic paraplegia with deafness,C2931291,C536692,312910,MONDO:0010732,spastic paraparesis-deafness syndrome,Spastic paraparesis co-occurrent with deafness (disorder) | Spastic paraparesis co-occurrent with deafness | Spastic paraparesis and deafness | Wells Jankovic syndrome
+BMGC_DS13645,BMG_DS052728,722206009,Yorifuji Okuno syndrome,,,,,,,C2931296,C536714,600001,MONDO:0010802,pancreatic hypoplasia-diabetes-congenital heart disease syndrome,"Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome (disorder) | Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome | Yorifuji Okuno syndrome"
+BMGC_DS13646,BMG_DS052731,716378008,Combined immunodeficiency due to ZAP70 deficiency,,,,,,,C2931299,,,,,Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency (disorder) | Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency | Combined immunodeficiency due to ZAP70 deficiency | Combined immunodeficiency due to ZAP70 (Zeta-chain associated protein kinase 70) deficiency
+BMGC_DS13647,BMG_DS052736,,Woods Leversha Rogers syndrome,,,,,,,C2931307,C536744,600546,MONDO:0010900,intrauterine growth retardation with increased mitomycin c sensitivity,
+BMGC_DS13648,BMG_DS052744,,T cell immunodeficiency primary,,,,,,,C2931320,C536780,,,,
+BMGC_DS13649,BMG_DS052754,,Glucose-6-phosphate translocase deficiency,,,,,,,C2931345,C536831,,MONDO:0023258,glycogen storage disease type 1 due to SLC37A4 mutation,
+BMGC_DS13650,BMG_DS052757,,Familial myelofibrosis,,,,,,,C2931351,C536848,,MONDO:0023119,familial myelofibrosis,
+BMGC_DS13651,BMG_DS052760,,"Spastic paraplegia 3, autosomal dominant",,,,,,,C2931355,C536864,182600,MONDO:0008437,hereditary spastic paraplegia 3A,
+BMGC_DS13652,BMG_DS052783,,Moyamoya disease 1,,,,,,,C2931384,C536991,252350,MONDO:0009649,moyamoya disease 1,
+BMGC_DS13653,BMG_DS052793,,"Bulbospinal neuronopathy, X-linked recessive",,,,,,,C2931395,C537017,,,,
+BMGC_DS13654,BMG_DS052798,,Familial lipomyelomeningocele,,,,,,,C2931400,C537030,,,,
+BMGC_DS13655,BMG_DS052799,1208866002,Long QT syndrome type 3,,,,,,,C2931401,C537034,,,,Long QT syndrome type 3 (disorder) | Long QT syndrome type 3
+BMGC_DS13656,BMG_DS052813,,Bare lymphocyte syndrome 2,,,,,,,C2931418,C537079,,,,
+BMGC_DS13657,BMG_DS052815,715470008,Brachydactylous dwarfism Mseleni type,,,,,,,C2931420,C537086,613342,MONDO:0013232,"brachydactylous dwarfism, Mseleni type",Mseleni joint disease | Brachydactylous dwarfism Mseleni type | Brachydactylous dwarfism Mseleni type (disorder)
+BMGC_DS13658,BMG_DS052819,,Orofaciodigital syndrome type1,,,,,,,C2931426,C537134,,,,
+BMGC_DS13659,BMG_DS052825,,Paraquat lung,,,,,,,C2931434,C537171,,,,
+BMGC_DS13660,BMG_DS052831,,"Hereditary spastic paralysis, infantile onset ascending",,,,,,,C2931441,C537217,607225,MONDO:0011797,infantile-onset ascending hereditary spastic paralysis,
+BMGC_DS13661,BMG_DS052845,,"Prosopagnosia, hereditary",,,,,,,C2931455,C537242,610382,MONDO:0012484,"prosopagnosia, hereditary",
+BMGC_DS13662,BMG_DS052846,,,,,,,,,C2931456,,176807,MONDO:0700275,"prostate cancer, hereditary",
+BMGC_DS13663,BMG_DS052848,,Lynch syndrome I (site-specific colonic cancer),,,,,,,C2931459,C537261,,,,
+BMGC_DS13664,BMG_DS052850,720612000,Forney Robinson Pascoe syndrome,,,,,,,C2931461,C537269,157800,MONDO:0008005,cardiospondylocarpofacial syndrome,Cardiospondylocarpofacial syndrome (disorder) | Cardiospondylocarpofacial syndrome | Forney syndrome | Forney Robinson Pascoe syndrome | Mitral regurgitation with deafness and skeletal anomalies syndrome
+BMGC_DS13665,BMG_DS052853,232373003,Goldblatt Viljoen syndrome,,,,,,,C2931464,C537280,179270,MONDO:0008358,radial ray hypoplasia-choanal atresia syndrome,Choanal atresia with radial ray hypoplasia | Choanal atresia with radial ray hypoplasia (disorder) | Goldblatt Viljoen syndrome
+BMGC_DS13666,BMG_DS052865,,Multiple system atrophy (MSA) with orthostatic hypotension,,,,,,,C2931478,C537381,,,,
+BMGC_DS13667,BMG_DS052867,,"Neurofibromatosis, Type 3, mixed central and peripheral",,,,,,,C2931480,C537389,162260,MONDO:0008080,"neurofibromatosis, type III, mixed central and peripheral",
+BMGC_DS13668,BMG_DS052869,,Neurofibromatosis-Noonan syndrome,,,,,DOID:0111683,neurofibromatosis-Noonan syndrome,C2931482,C537393,601321,MONDO:0011035,neurofibromatosis-Noonan syndrome,
+BMGC_DS13669,BMG_DS052875,,Zlotogora-Ogur syndrome,,,,,,,C2931488,C536726,225060,MONDO:0009151,cleft lip/palate-ectodermal dysplasia syndrome,
+BMGC_DS13670,BMG_DS052882,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 1",,,,,DOID:0112038,non-syndromic X-linked intellectual disability 1,C2931498,,309530;300522,MONDO:0010656,"intellectual disability, X-linked 1",
+BMGC_DS13671,BMG_DS052884,,Microphthalmia and mental deficiency,,,,,,,C2931500,C537462,,MONDO:0000170,"microphthalmia, isolated, with coloboma",
+BMGC_DS13672,BMG_DS052886,,"Microtia, meatal atresia and conductive deafness",,,,,,,C2931502,C537469,251800,MONDO:0009634,microtia with meatal atresia and conductive deafness,
+BMGC_DS13673,BMG_DS052942,,,,,,,,,C2931574,,,MONDO:0015571,deletion 5q35,
+BMGC_DS13674,BMG_DS052943,,Basaran Yilmaz syndrome,,,,,,,C2931577,C537660,,MONDO:0021979,Basaran Yilmaz syndrome,
+BMGC_DS13675,BMG_DS052949,1156813002,Gaucher-like disease,,,,,,,C2931585,C537675,,,,Gaucher disease with ophthalmoplegia and cardiovascular calcification (disorder) | Gaucher disease with ophthalmoplegia and cardiovascular calcification | Gaucher's disease type 3C | Gaucher-like disease | Cardiovascular Gaucher disease
+BMGC_DS13676,BMG_DS052980,,"Chromosome 8, monosomy 8p23 1",,,,,,,C2931638,C537827,,MONDO:0016658,8p23.1 microdeletion syndrome,
+BMGC_DS13677,BMG_DS052984,778042000,O'Donnell Pappas syndrome,,,,,,,C2931644,C537858,,MONDO:0016395,foveal hypoplasia-presenile cataract syndrome,O'Donnell Pappas syndrome | Foveal hypoplasia with presenile cataract syndrome | Foveal hypoplasia with presenile cataract syndrome (disorder)
+BMGC_DS13678,BMG_DS052987,,Laplane Fontaine Lagardere syndrome,,,,,,,C2931647,C537869,272450,MONDO:0010093,syndesmodysplasic dwarfism,
+BMGC_DS13679,BMG_DS052988,,"Larsen syndrome, dominant type",,,,,,,C2931648,C537873,,,,
+BMGC_DS13680,BMG_DS052996,,Phacomatosis pigmentokeratotica,,,,,,,C2931658,C537893,,MONDO:0017317,phakomatosis pigmentokeratotica,
+BMGC_DS13681,BMG_DS053000,722390006,Baraitser Brett Piesowicz syndrome,,,,,,,C2931662,C537905,,,,"Congenital intrauterine infection-like syndrome (disorder) | Congenital intrauterine infection-like syndrome | Baraitser Brett Piesowicz syndrome | Bilateral band-like calcification with polymicrogyria | Microcephaly, intracranial calcification, intellectual disability syndrome | Pseudo-TORCH syndrome"
+BMGC_DS13682,BMG_DS053007,,"Cerebral hemorrhage with amyloidosis, hereditary, Dutch type",,,,,,,C2931672,C537944,,MONDO:0015033,"ABeta amyloidosis, dutch type",
+BMGC_DS13683,BMG_DS053008,,"Ceroid lipofuscinosis, neuronal 1, infantile",,,,,,,C2931673,C537948,,,,
+BMGC_DS13684,BMG_DS053015,,"Camurati Engelmann disease, type 2",,,,,,,C2931683,C537978,606631,MONDO:0011690,"Camurati-Engelmann disease, type 2",
+BMGC_DS13685,BMG_DS053018,,"Charcot-Marie-Tooth disease, Type 1E",,,,,,,C2931686,C537986,,,,
+BMGC_DS13686,BMG_DS053019,,Dysferlinopathy,,,,G71.033,,,C2931687,C537995,,MONDO:0016145,qualitative or quantitative defects of dysferlin,
+BMGC_DS13687,BMG_DS053020,,,,,,,,,C2931689,,602668,MONDO:0011266,myotonic dystrophy type 2,
+BMGC_DS13688,BMG_DS053031,,"Deafness, autosomal dominant nonsyndromic sensorineural 17",,,,,,,C2931716,C538050,,,,
+BMGC_DS13689,BMG_DS053035,716022002,Fronto-facio-nasal dysplasia,,,,,,,C2931720,C538063,229400,MONDO:0009247,frontofacionasal dysplasia,Frontofacionasal dysplasia syndrome (disorder) | Frontofacionasal dysplasia syndrome | Gollop syndrome | Fronto-facio-nasal dysplasia
+BMGC_DS13690,BMG_DS053050,,Lactate dehydrogenase deficiency type A,,,,,,,C2931743,C538133,612933,MONDO:0013047,glycogen storage disease due to lactate dehydrogenase M-subunit deficiency,
+BMGC_DS13691,BMG_DS053053,40873003,Sulfocysteinuria,,,,,DOID:0111270,isolated sulfite oxidase deficiency,C2931746,C538141,,,,Sulfite oxidase deficiency syndrome | Sulfocysteinuria | Sulphocysteinuria | Sulphite oxidase deficiency syndrome | Sulfite oxidase deficiency syndrome (disorder)
+BMGC_DS13692,BMG_DS053062,,Acquired angioedema,,,,,DOID:0080941,acquired angioedema,C2931758,C538173,,MONDO:0019624,acquired angioedema,
+BMGC_DS13693,BMG_DS053066,,Acrofacial dysostosis Catania form,,,,,DOID:0060384,"acrofacial dysostosis, Catania type",C2931762,C538182,101805,MONDO:0007045,"acrofacial dysostosis, Catania type",
+BMGC_DS13694,BMG_DS053071,,"Deafness, autosomal dominant nonsyndromic sensorineural 22",,,,,,,C2931767,C538197,606346,MONDO:0011660,autosomal dominant nonsyndromic hearing loss 22,
+BMGC_DS13695,BMG_DS053082,,Adenosine monophosphate deaminase deficiency,,,,,,,C2931781,C538234,,MONDO:0013028,adenosine monophosphate deaminase deficiency,
+BMGC_DS13696,BMG_DS053083,,Amelogenesis imperfecta nephrocalcinosis,,,,,,,C2931783,C538241,204690;614253,MONDO:0008771,amelogenesis imperfecta type 1G,
+BMGC_DS13697,BMG_DS053084,,Amyloid angiopathy,,,,,,,C2931784,C538248,,,,
+BMGC_DS13698,BMG_DS053085,,"Amyotrophic lateral sclerosis, type 6",,,,,,,C2931786,C538251,608030,MONDO:0011951,amyotrophic lateral sclerosis type 6,
+BMGC_DS13699,BMG_DS053086,,,,,,,,,C2931787,,255960,MONDO:0009719,familial atrial myxoma,
+BMGC_DS13700,BMG_DS053087,,Atypical Hemolytic Uremic Syndrome,Atypical Hemolytic Uremic Syndrome,,,,DOID:0080301,atypical hemolytic-uremic syndrome,C2931788,D065766,,MONDO:0016244,atypical hemolytic-uremic syndrome,
+BMGC_DS13701,BMG_DS053098,,,,,,,,,C2931816,,,MONDO:0015566,2q24 microdeletion syndrome,
+BMGC_DS13702,BMG_DS053099,702357000,Chromosome 2q37 deletion syndrome,,,,,DOID:0111704,chromosome 2q37 deletion syndrome,C2931817,C538317,600430,MONDO:0010886,2q37 microdeletion syndrome,Chromosome 2q37 deletion syndrome | 2q37 deletion syndrome | Chromosome 2q37 deletion syndrome (disorder) | Brachydactyly mental retardation syndrome | Albright hereditary osteodystrophy-like syndrome
+BMGC_DS13703,BMG_DS053103,715491000,Nakamura Osame syndrome,,,,,,,C2931821,C538335,,,,"Autosomal recessive spastic paraplegia type 11 (disorder) | Autosomal recessive spastic paraplegia type 11 | Nakamura Osame syndrome | Spastic paraplegia, intellectual disability and thin corpus callosum"
+BMGC_DS13704,BMG_DS053104,,,,,,,,,C2931822,,,MONDO:0015459,nasopharyngeal carcinoma,
+BMGC_DS13705,BMG_DS053108,702355008,Potassium aggravated myotonia,,,,,,,C2931826,C538353,608390,MONDO:0018959,potassium-aggravated myotonia,Potassium aggravated myotonia (disorder) | Potassium aggravated myotonia | Sodium channel myotonia
+BMGC_DS13706,BMG_DS053112,,MacKay Shek Carr syndrome,,,,,,,C2931831,C538364,267760,MONDO:0009978,retinal degeneration-nanophthalmos-glaucoma syndrome,
+BMGC_DS13707,BMG_DS053113,,,,,,,,,C2931832,,256450,MONDO:0009734,"hyperinsulinemic hypoglycemia, familial, 1",
+BMGC_DS13708,BMG_DS053114,,,,,,,,,C2931833,,601820,MONDO:0011153,"hyperinsulinemic hypoglycemia, familial, 2",
+BMGC_DS13709,BMG_DS053115,717181004,Hyperprolinemia type 2,,,,,DOID:0080543,hyperprolinemia type 2,C2931835,C538385,239510,MONDO:0009401,hyperprolinemia type 2,Hyperprolinemia type 2 (disorder) | Hyperprolinemia type 2 | Hyperprolinaemia type 2 | Hyperprolinemia type II | Hyperprolinaemia type II
+BMGC_DS13710,BMG_DS053116,721838005,Familial hypertryptophanemia,,,,,DOID:0111703,familial hypertryptophanemia,C2931837,,600627,MONDO:0010907,familial hypertryptophanemia,Familial hypertryptophanemia (disorder) | Familial hypertryptophanemia | Familial hypertryptophanaemia
+BMGC_DS13711,BMG_DS053117,15346004,Familial HDL deficiency,,,,,,,C2931838,,,,,Familial hypoalphalipoproteinemia | Familial HDL deficiency | Familial high density lipoprotein deficiency | Alphalipoproteinemia neuropathy | Cholesterol thesaurismosis | Analphalipoproteinemia | Familial hypoalphalipoproteinaemia | Analphaliproteinaemia | A - alphalipoproteinaemia neuropathy | A - alphalipoproteinemia neuropathy | Analphaliproteinemia | Alphalipoproteinaemia neuropathy | Analphalipoproteinaemia | Familial hypoalphalipoproteinemia (disorder)
+BMGC_DS13712,BMG_DS053121,,Spinal muscular atrophy 4,,,,,,,C2931844,C538417,,,,
+BMGC_DS13713,BMG_DS053122,,Neurodegeneration with brain iron accumulation (NBIA),,,,,DOID:0110734,neurodegeneration with brain iron accumulation,C2931845,C538421,,MONDO:0018307,neurodegeneration with brain iron accumulation,
+BMGC_DS13714,BMG_DS053127,,Aase Smith syndrome 2,,,,,DOID:0111879,Diamond-Blackfan anemia 6,C2931850,C538442,612561,MONDO:0012937,Diamond-Blackfan anemia 6,
+BMGC_DS13715,BMG_DS053138,,Familial schizencephaly,,,,,,,C2931870,C538514,,MONDO:0018829,familial schizencephaly,
+BMGC_DS13716,BMG_DS053140,,Free sialic acid storage disease,,,,,,,C2931872,C538523,,MONDO:0019366,free sialic acid storage disease,
+BMGC_DS13717,BMG_DS053143,,Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells,,,,,,,C2931875,C538539,203300,MONDO:0008748,Hermansky-Pudlak syndrome 1,
+BMGC_DS13718,BMG_DS053149,,"Reticuloendotheliosis, familial, with eosinophilia",,,,,,,C2931884,C538564,,,,
+BMGC_DS13719,BMG_DS053152,,Pfeiffer type acrocephalosyndactyly,,,,,,,C2931888,C538582,,,,
+BMGC_DS13720,BMG_DS053155,,"Necrotizing encephalopathy, infantile subacute, of Leigh",,,,,,,C2931891,C538590,256000,MONDO:0009723,Leigh syndrome,
+BMGC_DS13721,BMG_DS053163,,Limb-girdle muscular dystrophy autosomal recessive,,,,,,,C2931907,C538640,,MONDO:0015152,autosomal recessive limb-girdle muscular dystrophy,
+BMGC_DS13722,BMG_DS053175,,Hyperkeratosis of the palms and soles and esophageal papillomas,,,,,DOID:0111708,focal nonepidermolytic palmoplantar keratoderma,C2931923,C538682,,MONDO:0017672,focal palmoplantar keratoderma,
+BMGC_DS13723,BMG_DS053178,240096000,Mitochondrial cytopathy,,,,,,,C2931928,C540770,,,,Mitochondrial cytopathy | Mitochondrial cytopathy (disorder) | Mitochondrial disease
+BMGC_DS13724,BMG_DS053182,,Gestational Diabetes Insipidus,,,,,DOID:0081057,gestational diabetes insipidus,C2932666,C548014,,MONDO:0023227,gestational diabetes insipidus,
+BMGC_DS13725,BMG_DS053184,,Inherited Peripheral Neuropathy,,,,,,,C2932678,C548028,,,,
+BMGC_DS13726,BMG_DS053187,,Pontocerebellar Hypoplasia Type 2,,,,,DOID:0112328,pontocerebellar hypoplasia type 2,C2932714,C548070,,MONDO:0016759,pontocerebellar hypoplasia type 2,
+BMGC_DS13727,BMG_DS053188,,Pseudohypoparathyroidism Type 1C,,,,,,,C2932716,C548076,612462,MONDO:0012911,pseudohypoparathyroidism type 1C,
+BMGC_DS13728,BMG_DS053189,,Pseudohypoparathyroidism Type 2,,,,,,,C2932717,C548077,203330,MONDO:0008749,pseudohypoparathyroidism type 2,
+BMGC_DS13729,BMG_DS053199,,Sarcoglycanopathies,Sarcoglycanopathies,,,,,,C2936331,D058088,,MONDO:0016140,sarcoglycanopathy,
+BMGC_DS13730,BMG_DS053200,,Alpha-Sarcoglycanopathies,Sarcoglycanopathies,,,,,,C2936332,D058088,608099,MONDO:0011968,autosomal recessive limb-girdle muscular dystrophy type 2D,
+BMGC_DS13731,BMG_DS053201,,22q11 Deletion Syndrome,22q11 Deletion Syndrome,,,,,,C2936346,D058165,,,,
+BMGC_DS13732,BMG_DS053202,,"46, XX Disorders of Sex Development","46, XX Disorders of Sex Development",,,,,,C2936403,D058489,,MONDO:0017576,"46,XX disorder of sex development",
+BMGC_DS13733,BMG_DS053203,,alpha-Dystroglycanopathies,Walker-Warburg Syndrome,,,,DOID:0050560,Walker-Warburg syndrome,C2936406,D058494,,MONDO:0018282,qualitative or quantitative defects of alpha-dystroglycan,
+BMGC_DS13734,BMG_DS053204,,"46, XX Testicular Disorders of Sex Development","46, XX Testicular Disorders of Sex Development",,,,DOID:0111760,"46,XX sex reversal",C2936419,D058531,,MONDO:0100249,"46,XX testicular disorder of sex development",
+BMGC_DS13735,BMG_DS053207,,Pyogenic Sacroiliitis,Sacroiliitis,,,,,,C2936444,D058566,,,,
+BMGC_DS13736,BMG_DS053208,,Septic Sacroiliitis,Sacroiliitis,,,,,,C2936445,D058566,,,,
+BMGC_DS13737,BMG_DS053210,,Chronic Liver Failure,End Stage Liver Disease,,,,,,C2936476,D058625,,MONDO:0100193,chronic liver failure,
+BMGC_DS13738,BMG_DS053211,,Familial CHARGE Syndrome,CHARGE Syndrome,,,,DOID:0050834,CHARGE syndrome,C2936502,D058747,,,,
+BMGC_DS13739,BMG_DS053215,,Acquired Hypogammaglobulinemia,Common Variable Immunodeficiency,,,,,,C2936664,D017074,,,,
+BMGC_DS13740,BMG_DS053216,,"Immunoglobulin Deficiency, Late-Onset",Common Variable Immunodeficiency,,,,,,C2936665,D017074,,,,
+BMGC_DS13741,BMG_DS053217,,Swyer Syndrome,"Gonadal Dysgenesis, 46,XY",,,,,,C2936694,D006061,,MONDO:0010765,"46,XY complete gonadal dysgenesis",
+BMGC_DS13742,BMG_DS053219,,Familial Kleine-Levin Syndrome,Kleine-Levin Syndrome,,,,DOID:0060165,Kleine-Levin syndrome,C2936703,D017593,,,,
+BMGC_DS13743,BMG_DS053220,,"Hyper-Immunoglobulin E Syndrome, Autosomal Dominant",Job Syndrome,,,,DOID:3261,hyper IgE recurrent infection syndrome 1,C2936739,D007589,,,,
+BMGC_DS13744,BMG_DS053221,,"48,XXYY Syndrome",Klinefelter Syndrome,,,,,,C2936741,D007713,,MONDO:0015028,"48,XXYY syndrome",
+BMGC_DS13745,BMG_DS053223,,,,,,,DOID:0060901,lymphoplasmacytic lymphoma,C2936755,,,,,
+BMGC_DS13746,BMG_DS053224,,Nevo syndrome,,,,,,,C2936777,C536113,,,,
+BMGC_DS13747,BMG_DS053226,,Hydroxymethylbilane Synthase Deficiency,"Porphyria, Acute Intermittent",,,,,,C2936779,D017118,,,,
+BMGC_DS13748,BMG_DS053227,,Generalized Myotonia of Thomsen,Myotonia Congenita,,,,,,C2936781,D009224,160800,MONDO:0009710;MONDO:0008055,"Thomsen and Becker disease | myotonia congenita, autosomal dominant",
+BMGC_DS13749,BMG_DS053228,,,,,,,DOID:0070271,Lynch syndrome 1,C2936783,,120435,MONDO:0007356,Lynch syndrome 1,
+BMGC_DS13750,BMG_DS053229,,"Antley-Bixler Syndrome, Autosomal Dominant",Antley-Bixler Syndrome Phenotype,,,,,,C2936791,D054882,207410,MONDO:0020667,Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis,
+BMGC_DS13751,BMG_DS053230,,Spinocerebellar ataxia 30,,,,,,,C2936793,C575214,613371,MONDO:0013241,spinocerebellar ataxia type 30,
+BMGC_DS13752,BMG_DS053232,,,,,,,DOID:0111261,fumarase deficiency,C2936826,,,,,
+BMGC_DS13753,BMG_DS053233,2298005;789156003,Focal facial dermal dysplasia,,,,,,,C2936827,,,MONDO:0018363,focal facial dermal dysplasia,Goltz syndrome | Focal dermal hypoplasia syndrome | Goltz-Gorlin syndrome | Goltz syndrome (disorder) | Goltz-Gorlin (dermal hypoplasia) syndrome | Goltz Gorlin syndrome | Focal facial dermal dysplasia (disorder) | Focal facial dermal dysplasia | FFDD - focal facial dermal dysplasia
+BMGC_DS13754,BMG_DS053234,,Keratosis of Greither,"Keratoderma, Palmoplantar, Epidermolytic",,,,,,C2936837,D053546,620411,MONDO:0957303,"palmoplantar keratoderma, epidermolytic, 2",
+BMGC_DS13755,BMG_DS053238,,Congenital adrenal hyperplasia due to 21 hydroxylase deficiency,,,,,,,C2936858,C535979,201910,MONDO:0008728,classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency,
+BMGC_DS13756,BMG_DS053239,723410002,N syndrome,,,,,DOID:0050769,N syndrome,C2936859,C536108,310465,MONDO:0010686,N syndrome,N syndrome (disorder) | N syndrome
+BMGC_DS13757,BMG_DS053240,,"Spastic paraplegia 25, autosomal recessive",,,,,,,C2936860,C536861,608220,MONDO:0011992,hereditary spastic paraplegia 25,
+BMGC_DS13758,BMG_DS053241,,Bardet-Biedl syndrome 1,,,,,DOID:0110123,Bardet-Biedl syndrome 1,C2936862,C537909,209900,MONDO:0008854,Bardet-Biedl syndrome 1,
+BMGC_DS13759,BMG_DS053242,,Bardet-Biedl syndrome 2,,,,,DOID:0110124,Bardet-Biedl syndrome 2,C2936863,C537910,615981,MONDO:0014432,Bardet-Biedl syndrome 2,
+BMGC_DS13760,BMG_DS053243,,Bardet-Biedl syndrome 4,,,,,DOID:0110126,Bardet-Biedl syndrome 4,C2936864,C537912,615982,MONDO:0014433,Bardet-Biedl syndrome 4,
+BMGC_DS13761,BMG_DS053245,,"SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT",,,,,,,C2936879,,613096,MONDO:0013132,hereditary spastic paraplegia 36,
+BMGC_DS13762,BMG_DS053246,,"Spastic Paraplegia 37, Autosomal Dominant",,,,,,,C2936880,C567931,611945,MONDO:0012766,hereditary spastic paraplegia 37,
+BMGC_DS13763,BMG_DS053250,,"Opitz GBBB Syndrome, X-Linked",,,,,,,C2936904,C567932,300000,MONDO:0010222,X-linked Opitz G/BBB syndrome,
+BMGC_DS13764,BMG_DS053252,17827007,Cross syndrome,,,,E70.328,,,C2936910,C537866,257800,MONDO:0009767,"oculocerebral hypopigmentation syndrome, Cross type",Cross syndrome | Oculocerebral-hypopigmentation syndrome | Cross syndrome (disorder) | Oculocerebral hypopigmentation syndrome Cross type | Kramer syndrome
+BMGC_DS13765,BMG_DS053259,52231000,Chronic ulcerative proctitis,,,,,,,C2937222,,,,,Chronic ulcerative proctitis | UC - Ulcerative colitis confined to rectum | Ulcerative colitis confined to rectum | Idiopathic proctitis | IP - Idiopathic proctitis | Chronic ulcerative proctitis (disorder)
+BMGC_DS13766,BMG_DS053262,49607006,Biotin deficiency disease,,,,,,,C2937225,,,MONDO:0020699,biotin metabolic disease,Biotin deficiency disease | Biotin deficiency disease (disorder)
+BMGC_DS13767,BMG_DS053267,,,,,,,DOID:3185,spinal cord glioma,C2937245,,,MONDO:0002542,spinal cord glioma,
+BMGC_DS13768,BMG_DS053273,,"THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT",,,,,,,C2937288,,188570;190160,MONDO:0008569,"thyroid hormone resistance, generalized, autosomal dominant",
+BMGC_DS13769,BMG_DS053274,193221009;111501005,Congenital hereditary muscular dystrophy,,,,,DOID:0050557,congenital muscular dystrophy,C2937300,,,,,Congenital hereditary muscular dystrophy | Congenital hereditary muscular dystrophy (disorder)
+BMGC_DS13770,BMG_DS053275,,,,,,,,,C2937358,,,MONDO:0013792,intracerebral hemorrhage,
+BMGC_DS13771,BMG_DS053276,80244009;398870000,Recurrent aphthous ulcer,,DA01.10,Oral aphthae or aphthalike ulceration,K12.0,,,C2937365,,,MONDO:0005318,canker sore,Recurrent aphthous ulcer | Periadenitis mucosa necrotica recurrens | Sutton's disease | Recurring scarring aphthae | Mikulicz's aphthae | Recurrent aphthous stomatitis | Aphthae major | RAS - Recurrent aphthous stomatitis | Recurrent aphthous ulceration | Recurrent aphthous ulcer (disorder) | Recurrent aphthous ulcer (disorder) | Recurrent aphthous ulcer | Recurrent aphthous ulceration
+BMGC_DS13772,BMG_DS053293,206523001;86092005;157154006,Meconium ileus,,,,,,,C2939175,,,MONDO:0054868,meconium ileus,Meconium ileus | Meconium obstruction | Meconium ileus (disorder) | Cystic fibrosis with meconium ileus | Meconium obstruction of intestine in mucoviscidosis | Meconium ileus of the newborn | Cystic fibrosis with meconium ileus (disorder) | Meconium ileus in cystic fibrosis | Meconium ileus | Meconium ileus (disorder)
+BMGC_DS13773,BMG_DS053310,,,,,,,,,C2939461,,,MONDO:0005170,myeloid neoplasm,
+BMGC_DS13774,BMG_DS053311,124134002,Deficiency of glucose-6-phosphate dehydrogenase,,,,,DOID:2862,glucosephosphate dehydrogenase deficiency,C2939465,,,MONDO:0005775,G6PD deficiency,Deficiency of glucose-6-phosphate dehydrogenase | Deficiency of glucose-6-phosphate dehydrogenase (disorder) | Deficiency of G-6PD (glucose-6-phosphate dehydrogenase) | G6PD - glucose-6-phosphate dehydrogenase deficiency
+BMGC_DS13775,BMG_DS053315,,Thyroid Hormone Resistance Syndrome,Thyroid Hormone Resistance Syndrome,,,,DOID:11633,thyroid hormone resistance syndrome,C2940786,D018382,,MONDO:0001328,thyroid hormone resistance syndrome,
+BMGC_DS13776,BMG_DS053327,21631000119105,Limb ischemia,,,,,,,C2945695,,,MONDO:0000491,limb ischemia,Limb ischaemia | Limb ischemia | Limb ischemia (disorder)
+BMGC_DS13777,BMG_DS053347,445780006,Infection caused by carbapenem resistant Acinetobacter,,,,,,,C2959527,,,,,Infection caused by carbapenem resistant Acinetobacter (disorder) | Infection caused by carbapenem resistant Acinetobacter
+BMGC_DS13778,BMG_DS053390,446903007,Fungal septicemia,,,,,,,C2960008,,,,,Septicemia due to fungus (disorder) | Fungal septicaemia | Fungal septicemia | Septicaemia due to fungus | Septicemia due to fungus
+BMGC_DS13779,BMG_DS053397,447117006,Hemoglobin H constant spring thalassemia,,,,,,,C2960096,,,,,Hemoglobin H constant spring thalassemia (disorder) | Haemoglobin H constant spring thalassaemia | Hemoglobin H constant spring thalassemia
+BMGC_DS13780,BMG_DS053408,,,,,,,,,C2960310,,265380,MONDO:0009934,alveolar capillary dysplasia with misalignment of pulmonary veins,
+BMGC_DS13781,BMG_DS053436,234969005,Dentinogenesis imperfecta without osteogenesis imperfecta,,,,,,,C2973527,,125490,MONDO:0007441,dentinogenesis imperfecta type 2,Hereditary opalescent dentine | Dentinogenesis imperfecta without osteogenesis imperfecta | Dentinogenesis imperfecta - Shield's type II | Dentinogenesis imperfecta - Shield's type II (disorder) | Capdepont teeth
+BMGC_DS13782,BMG_DS053439,11399002,Pulmonary arterial hypertension,,,,,,,C2973725,,MTHU037923,MONDO:0015924,pulmonary arterial hypertension,Pulmonary hypertensive arterial disease | Hypertensive pulmonary arterial disease | Pulmonary hypertensive arterial disease (disorder) | Pulmonary arterial hypertension
+BMGC_DS13783,BMG_DS053440,,Coxiella burnetii Infection,Q Fever,,,,,,C2973787,D011778,,,,
+BMGC_DS13784,BMG_DS053519,47382004;276206000,Superficial mycosis,,,,,DOID:0050133,superficial mycosis,C2980104,,,MONDO:0024268,superficial mycosis,Dermatophytosis | Tinea | Ringworm | Microsporic tinea | Dermatophytosis (disorder) | Superficial mycosis | Superficial mycosis (disorder)
+BMGC_DS13785,BMG_DS053524,193541000;71111008,Glaucoma of childhood,,9C61.4Z,"Developmental glaucoma, unspecified",Q15.0,,,C2981140,,,MONDO:0020367,juvenile open angle glaucoma,Glaucoma of childhood | Glaucoma of childhood (disorder) | Glaucoma of childhood | Infantile glaucoma | Juvenile glaucoma | Developmental glaucoma | Glaucoma of childhood (disorder)
+BMGC_DS13786,BMG_DS053526,,,,,,,,,C2981150,,,MONDO:0016064,cleft palate,
+BMGC_DS13787,BMG_DS053531,,,,,,,,,C2985219,,,MONDO:0016724,papillary tumor of the pineal region,
+BMGC_DS13788,BMG_DS053532,,Fetal Alcohol Spectrum Disorders,Fetal Alcohol Spectrum Disorders,,,,,,C2985290,D063647,,MONDO:0000408,fetal alcohol spectrum disorder,
+BMGC_DS13789,BMG_DS053533,772130002,Rhabdoid tumor predisposition syndrome,,,,,DOID:0070617,rhabdoid tumor predisposition syndrome,C2985524,,,MONDO:0016473,familial rhabdoid tumor,Rhabdoid tumour predisposition syndrome | Rhabdoid tumor predisposition syndrome | Rhabdoid tumor predisposition syndrome (disorder) | Familial rhabdoid tumor | Familial rhabdoid tumour
+BMGC_DS13790,BMG_DS053539,,,,,,,,,C2986658,,,MONDO:0006033,diffuse intrinsic pontine glioma,
+BMGC_DS13791,BMG_DS053540,,Congenital Bone Marrow Failure Syndromes,Congenital Bone Marrow Failure Syndromes,,,,,,C2986691,D000080984,,,,
+BMGC_DS13792,BMG_DS053541,,,,,,,,,C2986703,,,MONDO:0019716,overgrowth syndrome,
+BMGC_DS13793,BMG_DS053551,,,,,,,,,C3146244,,,MONDO:0000395,alcohol-related birth defect,
+BMGC_DS13794,BMG_DS053552,,"DEAFNESS, AUTOSOMAL RECESSIVE 76",,,,,,,C3147083,,615540;615535,MONDO:0014237,autosomal recessive nonsyndromic hearing loss 76,
+BMGC_DS13795,BMG_DS053553,,"DEAFNESS, AUTOSOMAL DOMINANT, WITH PERIPHERAL NEUROPATHY",,,,,,,C3148751,,603324,,,
+BMGC_DS13796,BMG_DS053554,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E",,,,,,,C3148763,,603511,,,
+BMGC_DS13797,BMG_DS053555,,"WOOLLY HAIR, AUTOSOMAL RECESSIVE 2, WITH OR WITHOUT HYPOTRICHOSIS",,,,,DOID:0110704,hypotrichosis 7,C3148823,,607365;604379,,,
+BMGC_DS13798,BMG_DS053556,,WH/HT,,,,,DOID:0110704,hypotrichosis 7,C3148824,,604379,,,
+BMGC_DS13799,BMG_DS053557,,"FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED",,,,,DOID:0060201,amyotrophic lateral sclerosis type 10,C3148872,,605078;612069,,,
+BMGC_DS13800,BMG_DS053558,,"USHER SYNDROME, TYPE IIC, GPR98/PDZD7 DIGENIC",,,,,,,C3148929,,602851;612971,,,
+BMGC_DS13801,BMG_DS053560,,"DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOPATHY",,,,,,,C3149009,,606346,,,
+BMGC_DS13802,BMG_DS053561,,"SEIZURES, BENIGN FAMILIAL NEONATAL, 1",,,,,,,C3149074,,121200;602235,MONDO:0007365,"seizures, benign familial neonatal, 1",
+BMGC_DS13803,BMG_DS053562,,"SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA",,,,,,,C3149075,,121200;602235,,,
+BMGC_DS13804,BMG_DS053563,,"GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE",,,,,,,C3149117,,138140;606777,,,
+BMGC_DS13805,BMG_DS053564,,"PARASOMNIA, SLEEPTALKING TYPE",,,,,,,C3149124,,606840,,,
+BMGC_DS13806,BMG_DS053567,,"CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KB",,,,,DOID:0060399,chromosome 16p12.1 deletion syndrome,C3149276,,136570,MONDO:0007631,"chromosome 16p12.1 deletion syndrome, 520kb",
+BMGC_DS13807,BMG_DS053568,,"IMMUNODEFICIENCY, COMMON VARIABLE, 1",,,,,DOID:0081144,common variable immunodeficiency 1,C3149378,,604558;607594,MONDO:0011864,"immunodeficiency, common variable, 1",
+BMGC_DS13808,BMG_DS053569,,"DERMATOFIBROSIS LENTICULARIS DISSEMINATA, ISOLATED",,,,,,,C3149399,,166700;607844,,,
+BMGC_DS13809,BMG_DS053570,,HYPERALPHALIPOPROTEINEMIA 1,,,,,,,C3149462,,143470;118470,,,
+BMGC_DS13810,BMG_DS053571,,,,,,,,,C3149494,,148100,MONDO:0007847,keloid formation,
+BMGC_DS13811,BMG_DS053572,,"LARYNGOSPASM, SEVERE NEONATAL EPISODIC",,,,,,,C3149517,,608390,MONDO:0800339,"laryngospasm, severe neonatal episodic",
+BMGC_DS13812,BMG_DS053574,,"DEAFNESS, AUTOSOMAL DOMINANT, WITHOUT VESTIBULAR INVOLVEMENT",,,,,,,C3149566,,606351;609006,,,
+BMGC_DS13813,BMG_DS053575,,"MELORHEOSTOSIS, ISOLATED",,,,,,,C3149631,,155950,MONDO:0007970,melorheostosis,
+BMGC_DS13814,BMG_DS053577,,Melorheostosis with Osteopoikilosis,,,,,,,C3149695,C563593,,MONDO:0015995,melorheostosis with osteopoikilosis,
+BMGC_DS13815,BMG_DS053579,,MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE),,,,,,,C3149750,,188250;609560,MONDO:0012301,"mitochondrial DNA depletion syndrome, myopathic form",
+BMGC_DS13816,BMG_DS053580,,CHROMOSOME 7q11.23 TRIPLICATION SYNDROME,,,,,DOID:0080926,7q11.23 duplication syndrome,C3149767,,609757,,,
+BMGC_DS13817,BMG_DS053582,,POLYCYSTIC KIDNEY DISEASE 1,,,,,,,C3149841,,601313;173900,MONDO:0008263,polycystic kidney disease 1,
+BMGC_DS13818,BMG_DS053583,,,,,,,,,C3149907,,,MONDO:0800224,"amyotrophic lateral sclerosis, susceptibility to, 13",
+BMGC_DS13819,BMG_DS053585,,"PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL",,,,,,,C3149931,,610644,MONDO:0012530,palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome,
+BMGC_DS13820,BMG_DS053586,,ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS,,,,,DOID:0050462,Antley-Bixler syndrome with disordered steroidogenesis,C3150099,,124015;201750,MONDO:0008726,Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis,
+BMGC_DS13821,BMG_DS053587,,BARDET-BIEDL SYNDROME 15,,,,,,,C3150127,,613580;615992,MONDO:0014443,Bardet-Biedl syndrome 15,
+BMGC_DS13822,BMG_DS053588,,"CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB",,,,,DOID:0070515,"chromosome 16p11.2 deletion syndrome, 593-kb",C3150154,,611913,MONDO:0012756,proximal 16p11.2 microdeletion syndrome,
+BMGC_DS13823,BMG_DS053589,,"IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS",,,,,,,C3150156,,611926,MONDO:0012757,"lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome",
+BMGC_DS13824,BMG_DS053590,,"FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, TARDBP-RELATED",,,,,DOID:0060201,amyotrophic lateral sclerosis type 10,C3150169,,612069,,,
+BMGC_DS13825,BMG_DS053591,,"FTLD-TDP, TARDBP-RELATED",,,,,DOID:0060201,amyotrophic lateral sclerosis type 10,C3150171,,612069,,,
+BMGC_DS13826,BMG_DS053592,,MITOCHONDRIAL DNA DEPLETION SYNDROME 8B (MNGIE TYPE),,,,,,,C3150172,,604712;612075,,,
+BMGC_DS13827,BMG_DS053593,,"AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE",,,,,DOID:0081138,agammaglobulinemia 6,C3150207,,612692,MONDO:0012987,"agammaglobulinemia 6, autosomal recessive",
+BMGC_DS13828,BMG_DS053594,,RETINITIS PIGMENTOSA 53,,,,,,,C3150208,,612712;608830,MONDO:0800348,retinitis pigmentosa 53,
+BMGC_DS13829,BMG_DS053595,,CHROMOSOME 6q24-q25 DELETION SYNDROME,,,,,DOID:0060424,chromosome 6q24-q25 deletion syndrome,C3150215,,612863,MONDO:0013025,chromosome 6q24-q25 deletion syndrome,
+BMGC_DS13830,BMG_DS053596,,COMPLEMENT COMPONENT C1r/C1s DEFICIENCY,,,,,,,C3150274,,216950,MONDO:0009005,complement component C1r/C1s deficiency,
+BMGC_DS13831,BMG_DS053597,,COMPLEMENT COMPONENT 2 DEFICIENCY,,,,,,,C3150275,,217000,MONDO:0009006,complement component 2 deficiency,
+BMGC_DS13832,BMG_DS053598,,"AICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT",,,,,,,C3150315,,225750;606609,,,
+BMGC_DS13833,BMG_DS053599,,"HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY",,,,,DOID:0051006,congenital nonspherocytic hemolytic anemia 5,C3150343,,142600;235700,MONDO:0009340,non-spherocytic hemolytic anemia due to hexokinase deficiency,
+BMGC_DS13834,BMG_DS053600,,"HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED",,,,,,,C3150344,,236200;613381,,,
+BMGC_DS13835,BMG_DS053602,,"IMMUNODEFICIENCY, COMMON VARIABLE, 2",,,,,DOID:0081145,common variable immunodeficiency 2,C3150354,,240500;604907,MONDO:0009413,"immunodeficiency, common variable, 2",
+BMGC_DS13836,BMG_DS053604,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2",,,,,DOID:0111240,congenital muscular dystrophy-dystroglycanopathy type A2,C3150411,,607439;613150,MONDO:0013154,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2",
+BMGC_DS13837,BMG_DS053605,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 3",,,,,DOID:0112378,muscular dystrophy-dystroglycanopathy type B3,C3150412,,606822;613151,MONDO:0013155,"muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3",
+BMGC_DS13838,BMG_DS053606,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5",,,,,DOID:0111241,congenital muscular dystrophy-dystroglycanopathy type A5,C3150413,,606596;613153,MONDO:0013157,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5",
+BMGC_DS13839,BMG_DS053607,,,,,,,,,C3150414,,613154,MONDO:0013158,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6",
+BMGC_DS13840,BMG_DS053608,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 2",,,,,DOID:0112380,muscular dystrophy-dystroglycanopathy type B2,C3150416,,607439;613156,MONDO:0013160,"muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2",
+BMGC_DS13841,BMG_DS053609,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3",,,,,,,C3150417,,606822;613157,MONDO:0013161,autosomal recessive limb-girdle muscular dystrophy type 2O,
+BMGC_DS13842,BMG_DS053610,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2",,,,,,,C3150418,,607439;613158,MONDO:0013162,autosomal recessive limb-girdle muscular dystrophy type 2N,
+BMGC_DS13843,BMG_DS053611,,NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1,,,,,DOID:0111117,nephronophthisis-like nephropathy 1,C3150419,,613159;613553,MONDO:0013163,nephronophthisis-like nephropathy 1,
+BMGC_DS13844,BMG_DS053614,,"EPILEPSY, HOT WATER, 2",,,,,DOID:0081107,hot water epilepsy 2,C3150536,,613340,MONDO:0013230,"epilepsy, hot water, 2",
+BMGC_DS13845,BMG_DS053616,,,,,,,,,C3150546,,613347,MONDO:0013235,"pancreatic cancer, susceptibility to, 2",
+BMGC_DS13846,BMG_DS053617,,,,,,,,,C3150547,,613348,MONDO:0013236,"pancreatic cancer, susceptibility to, 3",
+BMGC_DS13847,BMG_DS053618,,"MONONEUROPATHY OF THE MEDIAN NERVE, MILD",,,,,,,C3150596,,613353;608206,MONDO:0013237,"susceptibility to mononeuropathy of the median nerve, mild",
+BMGC_DS13848,BMG_DS053619,,CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME,,,,,,,C3150607,,613355,MONDO:0013238,chromosome 17q23.1-q23.2 deletion syndrome,
+BMGC_DS13849,BMG_DS053620,609577006,"Maturity-onset diabetes of the young, type 10",,,,,,,C3150617,,613370,MONDO:0013240,maturity-onset diabetes of the young type 10,"Maturity-onset diabetes of the young, type 10 (disorder) | Maturity-onset diabetes of the young, type 10 | MODY10 (maturity-onset diabetes of the young type 10)"
+BMGC_DS13850,BMG_DS053621,609578001,"Maturity-onset diabetes of the young, type 11",,,,,,,C3150618,,613375,MONDO:0013242,maturity-onset diabetes of the young type 11,"Maturity-onset diabetes of the young, type 11 | Maturity-onset diabetes of the young, type 11 (disorder) | MODY11 (maturity-onset diabetes of the young type 11)"
+BMGC_DS13851,BMG_DS053622,,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 4",,,,,DOID:0111209,autosomal dominant distal hereditary motor neuronopathy 4,C3150619,,604624;613376,MONDO:0013243,"neuronopathy, distal hereditary motor, type 2C",
+BMGC_DS13852,BMG_DS053623,,"BRACHYDACTYLY, TYPE E2",,,,,DOID:0110976,brachydactyly type E2,C3150644,,168470;613382,MONDO:0013244,brachydactyly type E2,
+BMGC_DS13853,BMG_DS053624,,"AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM",,,,,,,C3150649,,606409;613385,MONDO:0013245,syndromic multisystem autoimmune disease due to ITCH deficiency,
+BMGC_DS13854,BMG_DS053625,,,,,,,,,C3150651,,613387,MONDO:0013246,"fatty liver disease, nonalcoholic, susceptibility to, 2",
+BMGC_DS13855,BMG_DS053626,,FANCONI RENOTUBULAR SYNDROME 2,,,,,DOID:0080758,Fanconi renotubular syndrome 2,C3150652,,182309;613388,MONDO:0013247,Fanconi renotubular syndrome 2,
+BMGC_DS13856,BMG_DS053627,,"FANCONI ANEMIA, COMPLEMENTATION GROUP O",,,,,DOID:0111096,Fanconi anemia complementation group O,C3150653,,602774;613390,MONDO:0013248,Fanconi anemia complementation group O,
+BMGC_DS13857,BMG_DS053628,,"DEAFNESS, AUTOSOMAL RECESSIVE 84A",,,,,,,C3150654,,603317;613391,MONDO:0013249,autosomal recessive nonsyndromic hearing loss 84A,
+BMGC_DS13858,BMG_DS053629,,BIRBECK GRANULE DEFICIENCY,,,,,,,C3150657,,604862;613393,MONDO:0013251,Birbeck granule deficiency,
+BMGC_DS13859,BMG_DS053630,,WARSAW BREAKAGE SYNDROME,,,,,DOID:0060535,Warsaw breakage syndrome,C3150658,,601150;613398,MONDO:0013252,Warsaw breakage syndrome,
+BMGC_DS13860,BMG_DS053631,,,,,,,,,C3150659,,613399,MONDO:0013253,"breast-ovarian cancer, familial, susceptibility to, 3",
+BMGC_DS13861,BMG_DS053634,,"MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY",,,,,DOID:0080457,"microcephaly, seizures, and developmental delay",C3150667,,605610;613402,MONDO:0013254,"microcephaly, seizures, and developmental delay",
+BMGC_DS13862,BMG_DS053635,,"ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2",,,,,DOID:0111354,"arthrogryposis, renal dysfunction, and cholestasis 2",C3150672,,613401;613404,MONDO:0013255,"arthrogryposis, renal dysfunction, and cholestasis 2",
+BMGC_DS13863,BMG_DS053636,,CHROMOSOME 15q24 DELETION SYNDROME,,,,,,,C3150674,,613406,MONDO:0013256,chromosome 15q24 deletion syndrome,
+BMGC_DS13864,BMG_DS053637,,CHROMOSOME 15q24 DUPLICATION SYNDROME,,,,,,,C3150675,,613406,,,
+BMGC_DS13865,BMG_DS053639,,,,,,,,,C3150677,,613410,MONDO:0013258,"autism, susceptibility to, 16",
+BMGC_DS13866,BMG_DS053640,,OGUCHI DISEASE 2,,,,,DOID:0110713,Oguchi disease-2,C3150678,,180381;613411,MONDO:0013259,Oguchi disease-2,
+BMGC_DS13867,BMG_DS053641,,"ESOPHAGITIS, EOSINOPHILIC, 2",,,,,,,C3150679,,613412,MONDO:0013260,"esophagitis, eosinophilic, 2",
+BMGC_DS13868,BMG_DS053642,,"CARDIOMYOPATHY, DILATED, 1R",,,,,,,C3150681,,102540;613424,MONDO:0013261,dilated cardiomyopathy 1R,
+BMGC_DS13869,BMG_DS053643,,LEFT VENTRICULAR NONCOMPACTION 4,,,,,,,C3150682,,102540;613424,MONDO:0800350,left ventricular noncompaction 4,
+BMGC_DS13870,BMG_DS053644,,LEFT VENTRICULAR NONCOMPACTION 5,,,,,,,C3150690,,160760;613426,MONDO:0800351,left ventricular noncompaction 5,
+BMGC_DS13871,BMG_DS053645,,RETINITIS PIGMENTOSA 54,,,,,,,C3150691,,613425;613428,MONDO:0013263,retinitis pigmentosa 54,
+BMGC_DS13872,BMG_DS053646,,AMYOTROPHIC LATERAL SCLEROSIS 12,,,,,,,C3150692,,602432;613435,MONDO:0013264,amyotrophic lateral sclerosis type 12,
+BMGC_DS13873,BMG_DS053647,,,,,,,,,C3150693,,613436,MONDO:0013265,"autism, susceptibility to, 17",
+BMGC_DS13874,BMG_DS053648,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE",,,,,DOID:0070050,"neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language",C3150700,,600662;613443,MONDO:0013266,"intellectual disability, autosomal dominant 20",
+BMGC_DS13875,BMG_DS053649,,"CHROMOSOME 16p11.2 DELETION SYNDROME, 220-KB",,,,,DOID:0060398,"chromosome 16p11.2 deletion syndrome, 220-kb",C3150701,,613444,MONDO:0013267,distal 16p11.2 microdeletion syndrome,
+BMGC_DS13876,BMG_DS053650,,FRONTONASAL DYSPLASIA 2,,,,,DOID:0081046,frontonasal dysplasia 2,C3150703,,613451;605420,MONDO:0013268,frontonasal dysplasia with alopecia and genital anomaly,
+BMGC_DS13877,BMG_DS053651,,"DEAFNESS, AUTOSOMAL RECESSIVE 91",,,,,,,C3150704,,173321;613453,MONDO:0013269,autosomal recessive nonsyndromic hearing loss 91,
+BMGC_DS13878,BMG_DS053652,702450004,FOXG1 syndrome,,,,,,,C3150705,,613454,MONDO:0013270,"Rett syndrome, congenital variant",FOXG1 syndrome | FOXG1 syndrome (disorder)
+BMGC_DS13879,BMG_DS053653,,FRONTONASAL DYSPLASIA 3,,,,,DOID:0081047,frontonasal dysplasia 3,C3150706,,601527;613456,MONDO:0013271,frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome,
+BMGC_DS13880,BMG_DS053654,,CHROMOSOME 14q11-q22 DELETION SYNDROME,,,,,DOID:0060392,chromosome 14q11-q22 deletion syndrome,C3150707,,613457,MONDO:0013272,chromosome 14q11-q22 deletion syndrome,
+BMGC_DS13881,BMG_DS053655,,CHROMOSOME 16p13.3 DUPLICATION SYNDROME,,,,,,,C3150708,,613458,MONDO:0013273,chromosome 16p13.3 duplication syndrome,
+BMGC_DS13882,BMG_DS053656,,RETINITIS PIGMENTOSA 51,,,,,,,C3150715,,608132;613464,MONDO:0013274,retinitis pigmentosa 51,
+BMGC_DS13883,BMG_DS053657,,"HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY",,,,,DOID:0051005,congenital nonspherocytic hemolytic anemia 4,C3150730,,172400;613470,MONDO:0013275,hemolytic anemia due to glucophosphate isomerase deficiency,
+BMGC_DS13884,BMG_DS053658,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 5,,,,,DOID:0080438,developmental and epileptic encephalopathy 5,C3150731,,182810;613477,MONDO:0013277,"developmental and epileptic encephalopathy, 5",
+BMGC_DS13885,BMG_DS053659,,LONG QT SYNDROME 13,,,,,,,C3150733,,600734;613485,MONDO:0013279,long QT syndrome 13,
+BMGC_DS13886,BMG_DS053660,,Antibody Deficiency due to Defect in CD19,,,,,,,C3150738,C566275,613493,MONDO:0013283,"immunodeficiency, common variable, 3",
+BMGC_DS13887,BMG_DS053661,,"IMMUNODEFICIENCY, COMMON VARIABLE, 4",,,,,DOID:0081147,common variable immunodeficiency 4,C3150739,,613494;606269,MONDO:0013284,"immunodeficiency, common variable, 4",
+BMGC_DS13888,BMG_DS053662,,"IMMUNODEFICIENCY, COMMON VARIABLE, 5",,,,,DOID:0081148,common variable immunodeficiency 5,C3150740,,613495;112210,MONDO:0013285,"immunodeficiency, common variable, 5",
+BMGC_DS13889,BMG_DS053663,,"IMMUNODEFICIENCY, COMMON VARIABLE, 6",,,,,DOID:0081149,common variable immunodeficiency 6,C3150741,,613496;186845,MONDO:0013286,"immunodeficiency, common variable, 6",
+BMGC_DS13890,BMG_DS053664,,"AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE",,,,,DOID:0081135,agammaglobulinemia 2,C3150750,,146770;613500,MONDO:0013287,"agammaglobulinemia 2, autosomal recessive",
+BMGC_DS13891,BMG_DS053665,,"AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE",,,,,DOID:0081137,agammaglobulinemia 3,C3150751,,613501,MONDO:0013288,"agammaglobulinemia 3, autosomal recessive",
+BMGC_DS13892,BMG_DS053666,,"AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE",,,,,DOID:0060027,agammaglobulinemia 4,C3150752,,604515;613502,MONDO:0013289,"agammaglobulinemia 4, autosomal recessive",
+BMGC_DS13893,BMG_DS053667,,"AGAMMAGLOBULINEMIA 5, AUTOSOMAL DOMINANT",,,,,DOID:0080588,agammaglobulinemia 5,C3150753,,613506,MONDO:0013290,"agammaglobulinemia 5, autosomal dominant",
+BMGC_DS13894,BMG_DS053668,,GLYCOGEN STORAGE DISEASE XV,,,,,DOID:0050579,glycogen storage disease XV,C3150754,,613507;603942,MONDO:0013291,glycogen storage disease XV,
+BMGC_DS13895,BMG_DS053669,,CHROMOSOME 4q21 DELETION SYNDROME,,,,,DOID:0060420,chromosome 4q21 deletion syndrome,C3150756,,613509,MONDO:0013292,chromosome 4q21 deletion syndrome,
+BMGC_DS13896,BMG_DS053670,,"MICROPHTHALMIA, ISOLATED 6",,,,,,,C3150757,,613517;613858,MONDO:0013293,isolated microphthalmia 6,
+BMGC_DS13897,BMG_DS053672,,"DERMATITIS, ATOPIC, 8",,,,,DOID:0110104,atopic dermatitis 8,C3150763,,613518,MONDO:0013294,"dermatitis, atopic, 8",
+BMGC_DS13898,BMG_DS053673,,"DERMATITIS, ATOPIC, 9",,,,,DOID:0110105,atopic dermatitis 9,C3150764,,613519,MONDO:0013295,"dermatitis, atopic, 9",
+BMGC_DS13899,BMG_DS053674,,,,,,,,,C3150773,,613523,MONDO:0013296,myeloid neoplasm associated with FGFR1 rearrangement,
+BMGC_DS13900,BMG_DS053675,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H",,,,,,,C3150786,,613530,MONDO:0013297,autosomal dominant limb-girdle muscular dystrophy type 1H,
+BMGC_DS13901,BMG_DS053676,,CHROMOSOME 6q11-q14 DELETION SYNDROME,,,,,DOID:0060423,chromosome 6q11-q14 deletion syndrome,C3150790,,613544,MONDO:0013299,chromosome 6q11-q14 deletion syndrome,
+BMGC_DS13902,BMG_DS053677,,CHROMOSOME 6q13-q14 DELETION SYNDROME,,,,,DOID:0060423,chromosome 6q11-q14 deletion syndrome,C3150791,,613544,,,
+BMGC_DS13903,BMG_DS053679,,NEPHRONOPHTHISIS 11,,,,,DOID:0111118,nephronophthisis 11,C3150796,,609884;613550,MONDO:0013302,nephronophthisis 11,
+BMGC_DS13904,BMG_DS053680,,,,,,,,,C3150797,,613551,MONDO:0013303,"autoimmune disease, susceptibility to, 6",
+BMGC_DS13905,BMG_DS053681,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7,,,,,DOID:0111487,combined oxidative phosphorylation deficiency 7,C3150801,,613559;613541,MONDO:0013306,combined oxidative phosphorylation defect type 7,
+BMGC_DS13906,BMG_DS053682,,"MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2",,,,,DOID:0111186,"myopathy, lactic acidosis, and sideroblastic anemia 2",C3150802,,610957;613561,MONDO:0013307,"myopathy, lactic acidosis, and sideroblastic anemia 2",
+BMGC_DS13907,BMG_DS053683,,,,,,,,,C3150803,,613563,MONDO:0013308,CBL-related disorder,
+BMGC_DS13908,BMG_DS053684,,CHROMOSOME 2p12-p11.2 DELETION SYNDROME,,,,,DOID:0060414,chromosome 2p12-p11.2 deletion syndrome,C3150804,,613564,MONDO:0013309,chromosome 2p12-p11.2 deletion syndrome,
+BMGC_DS13909,BMG_DS053685,,ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1,,,,,,,C3150807,,613573;609607,MONDO:0024565,ectodermal dysplasia-syndactyly syndrome 1,
+BMGC_DS13910,BMG_DS053686,,RETINITIS PIGMENTOSA 55,,,,,,,C3150808,,608845;613575,MONDO:0013312,retinitis pigmentosa 55,
+BMGC_DS13911,BMG_DS053687,,ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2,,,,,,,C3150809,,613576,MONDO:0013313,ectodermal dysplasia-cutaneous syndactyly syndrome,
+BMGC_DS13912,BMG_DS053688,,RETINITIS PIGMENTOSA 56,,,,,,,C3150819,,607056;613581,MONDO:0013314,retinitis pigmentosa 56,
+BMGC_DS13913,BMG_DS053689,,RETINITIS PIGMENTOSA 57,,,,,,,C3150821,,180073;613582,MONDO:0013315,retinitis pigmentosa 57,
+BMGC_DS13914,BMG_DS053690,,OCCULT MACULAR DYSTROPHY,,,,,DOID:0050578,occult macular dystrophy,C3150833,,608581;613587,MONDO:0013316,occult macular dystrophy,
+BMGC_DS13915,BMG_DS053692,,,,,,,,,C3150852,,613601,MONDO:0013318,early repolarization associated with ventricular fibrillation,
+BMGC_DS13916,BMG_DS053693,,CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME,,,,,,,C3150857,,613603,MONDO:0013319,chromosome 4Q32.1-q32.2 triplication syndrome,
+BMGC_DS13917,BMG_DS053694,,"CHROMOSOME 16p12.2-p11.2 DELETION SYNDROME, 7.1- TO 8.7-MB",,,,,,,C3150858,,613604,MONDO:0013320,chromosome 16p12.2-p11.2 deletion syndrome,
+BMGC_DS13918,BMG_DS053695,,FORSYTHE-WAKELING SYNDROME,,,,,,,C3150859,,613606,MONDO:0013321,forsythe-wakeling syndrome,
+BMGC_DS13919,BMG_DS053696,,"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3",,,,,DOID:0111695,familial adult myoclonic epilepsy 3,C3150860,,613608;613297,MONDO:0013322,"epilepsy, familial adult myoclonic, 3",
+BMGC_DS13920,BMG_DS053697,,CRANIOECTODERMAL DYSPLASIA 2,,,,,DOID:0080804,cranioectodermal dysplasia 2,C3150874,,613602;613610,MONDO:0013323,cranioectodermal dysplasia 2,
+BMGC_DS13921,BMG_DS053698,1204421005,"Lymphedema, posterior choanal atresia syndrome",,,,,,,C3150875,,613611,MONDO:0013324,lymphedema-posterior choanal atresia syndrome,"Lymphedema, posterior choanal atresia syndrome (disorder) | Lymphedema, posterior choanal atresia syndrome | Lymphoedema, posterior choanal atresia syndrome"
+BMGC_DS13922,BMG_DS053699,721100009,COG5 congenital disorder of glycosylation,,,,,,,C3150876,,613612,MONDO:0013325,COG5-congenital disorder of glycosylation,Component of oligomeric golgi complex 5 congenital disorder of glycosylation (disorder) | COG5 (component of oligomeric golgi complex 5) congenital disorder of glycosylation | Component of oligomeric golgi complex 5 congenital disorder of glycosylation | COG5 congenital disorder of glycosylation | Carbohydrate deficient glycoprotein syndrome type IIi | Congenital disorder of glycosylation type IIi | CDG2I - carbohydrate deficient glycoprotein syndrome type IIi
+BMGC_DS13923,BMG_DS053700,,SENIOR-LOKEN SYNDROME 7,,,,,,,C3150877,,613524;613615,MONDO:0013326,Senior-Loken syndrome 7,
+BMGC_DS13924,BMG_DS053701,734990008,Primary hyperoxaluria type III,,,,,DOID:0111672,primary hyperoxaluria type 3,C3150878,,613616,MONDO:0013327,primary hyperoxaluria type 3,Primary hyperoxaluria type III (disorder) | Primary hyperoxaluria type 3 | Primary hyperoxaluria type III
+BMGC_DS13925,BMG_DS053702,,RETINITIS PIGMENTOSA 58,,,,,,,C3150879,,613598;613617,MONDO:0013328,retinitis pigmentosa 58,
+BMGC_DS13926,BMG_DS053703,,CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME,,,,,,,C3150880,,613618,MONDO:0013329,familial clubfoot due to 17q23.1q23.2 microduplication,
+BMGC_DS13927,BMG_DS053705,,"FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2",,,,,,,C3150889,,607788;613625,MONDO:0013331,"factor 5 and Factor VIII, combined deficiency of, 2",
+BMGC_DS13928,BMG_DS053707,1220575002,Fetal encasement syndrome,,,,,,,C3150891,,613630,MONDO:0013334,cocoon syndrome,Cocoon syndrome | Foetal encasement syndrome | Fetal encasement syndrome (disorder) | Fetal encasement syndrome
+BMGC_DS13929,BMG_DS053709,764440006,19p13.13 microdeletion syndrome,,,,,,,C3150894,,613638,MONDO:0013336,chromosome 19p13.13 deletion syndrome,Monosomy 19p13.13 | 19p13.13 microdeletion syndrome (disorder) | 19p13.13 microdeletion syndrome | Chromosome 19p13.13 deletion syndrome
+BMGC_DS13930,BMG_DS053710,,CHROMOSOME 19p13.13 DUPLICATION SYNDROME,,,,,DOID:0060426,chromosome 19p13.13 deletion syndrome,C3150895,,613638,,,
+BMGC_DS13931,BMG_DS053711,860814001,Hereditary sensory autonomic neuropathy type IC,,,,,,,C3150896,,613640,MONDO:0013337,"neuropathy, hereditary sensory and autonomic, type 1C",Hereditary sensory autonomic neuropathy type IC (disorder) | Hereditary sensory autonomic neuropathy type IC
+BMGC_DS13932,BMG_DS053712,,"CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B",,,,,,,C3150897,,601421;613641,MONDO:0013338,Charcot-Marie-Tooth disease recessive intermediate B,
+BMGC_DS13933,BMG_DS053713,,"CARDIOMYOPATHY, DILATED, 1GG",,,,,,,C3150898,,613642;600857,MONDO:0013339,dilated cardiomyopathy 1GG,
+BMGC_DS13934,BMG_DS053714,,,,,,,,,C3150899,,613643,MONDO:0013340,"Parkinson disease 5, autosomal dominant, susceptibility to",
+BMGC_DS13935,BMG_DS053715,,"SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE",,,,,,,C3150901,,613647;613653,MONDO:0013342,hereditary spastic paraplegia 48,
+BMGC_DS13936,BMG_DS053716,,C1q DEFICIENCY 1,,,,,,,C3150902,,120550;613652,MONDO:0013343,C1Q deficiency,
+BMGC_DS13937,BMG_DS053717,,D-2-HYDROXYGLUTARIC ACIDURIA 2,,,,,DOID:0111352,D-2-hydroxyglutaric aciduria 2,C3150909,,147650;613657,MONDO:0013345,d-2-hydroxyglutaric aciduria 2,
+BMGC_DS13938,BMG_DS053718,720576001,Brain calcification Rajab type,,,,,,,C3150910,,,MONDO:0100214,Rajab interstitial lung disease with brain calcifications,Brain calcification Rajab type (disorder) | Brain calcification Rajab type | Rajab syndrome
+BMGC_DS13939,BMG_DS053719,,CONE-ROD DYSTROPHY 15,,,,,DOID:0111021,cone-rod dystrophy 15,C3150912,,609502;613660,MONDO:0013348,cone-rod dystrophy 15,
+BMGC_DS13940,BMG_DS053720,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip",,,,,DOID:0080567,congenital disorder of glycosylation Ip,C3150913,,613661;613666,MONDO:0013349,ALG11-congenital disorder of glycosylation,
+BMGC_DS13941,BMG_DS053721,,MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE),,,,,DOID:0080123,mitochondrial DNA depletion syndrome 4b,C3150914,,613662;174763,MONDO:0013350,mitochondrial DNA depletion syndrome 4b,
+BMGC_DS13942,BMG_DS053722,,"MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY",,,,,DOID:0111262,infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly,C3150921,,603810;613668,MONDO:0013351,infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly,
+BMGC_DS13943,BMG_DS053723,1222706005,"Anterior maxillary protrusion, strabismus, intellectual disability syndrome",,,,,,,C3150924,,613671,MONDO:0013353,"intellectual disability, anterior maxillary protrusion, and strabismus","Anterior maxillary protrusion, strabismus, intellectual disability syndrome (disorder) | MRAMS (mental retardation, anterior maxillary protrusion, strabismus) syndrome | Anterior maxillary protrusion, strabismus, intellectual disability syndrome | MRAMS syndrome"
+BMGC_DS13944,BMG_DS053724,,"SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE",,,,,DOID:0050943,spastic ataxia 4,C3150925,,613672;613669,MONDO:0013354,spastic ataxia 4,
+BMGC_DS13945,BMG_DS053725,719453009,Congenital dyserythropoietic anemia type IV,,,,,DOID:0111400,congenital dyserythropoietic anemia type IVa,C3150926,,613673,MONDO:0013355,congenital dyserythropoietic anemia type 4,Congenital dyserythropoietic anemia type IV (disorder) | Congenital dyserythropoietic anemia type IV | Congenital dyserythropoietic anaemia type IV | Congenital dyserythropoietic anemia type 4 | Congenital dyserythropoietic anaemia type 4
+BMGC_DS13946,BMG_DS053726,,VESICOURETERAL REFLUX 3,,,,,,,C3150927,,613674;610928,MONDO:0013356,vesicoureteral reflux 3,
+BMGC_DS13947,BMG_DS053727,773554009,THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome,,,,,,,C3150939,,613680,MONDO:0013362,THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome,"THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome | THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome | Beaulieu Boycott Innes syndrome | THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome (disorder) | BBIS - Beaulieu Boycott Innes syndrome"
+BMGC_DS13948,BMG_DS053728,,CHROMOSOME 2q31.1 DUPLICATION SYNDROME,,,,,DOID:0060458,chromosome 2q31.1 duplication syndrome,C3150940,,613681,MONDO:0013363,chromosome 2q31.1 duplication syndrome,
+BMGC_DS13949,BMG_DS053729,,RUBINSTEIN-TAYBI SYNDROME 2,,,,,,,C3150941,,602700;613684,MONDO:0013364,Rubinstein-Taybi syndrome due to EP300 haploinsufficiency,
+BMGC_DS13950,BMG_DS053730,,"SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE",,,,,DOID:0112364,spondylocostal dysostosis 4,C3150942,,613686,MONDO:0013366,"spondylocostal dysostosis 4, autosomal recessive",
+BMGC_DS13951,BMG_DS053731,,Long Qt Syndrome 2,,,,,DOID:0110645,long QT syndrome 2,C3150943,C563614,613688,MONDO:0013367,long QT syndrome 2,
+BMGC_DS13952,BMG_DS053732,,MAMMARY-DIGITAL-NAIL SYNDROME,,,,,,,C3150946,,613689,MONDO:0013368,mammary-digital-nail syndrome,
+BMGC_DS13953,BMG_DS053733,,Long Qt Syndrome 6,,,,,DOID:0110648,long QT syndrome 6,C3150953,C566333,613693,MONDO:0013370,long QT syndrome 6,
+BMGC_DS13954,BMG_DS053734,,"Cardiomyopathy, Dilated, 1V",,,,,,,C3150958,C566856,613697,MONDO:0013373,dilated cardiomyopathy 1V,
+BMGC_DS13955,BMG_DS053735,,"KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT",,,,,DOID:0080591,Klippel-Feil syndrome 3,C3150967,,606522;613702,MONDO:0013375,"Klippel-Feil syndrome 3, autosomal dominant",
+BMGC_DS13956,BMG_DS053736,,,,,,,,,C3150968,,613703,MONDO:0013376,"microphthalmia, isolated, with coloboma 6",
+BMGC_DS13957,BMG_DS053737,,"MICROPHTHALMIA, ISOLATED 7",,,,,,,C3150969,,606522;613704,MONDO:0013377,isolated microphthalmia 7,
+BMGC_DS13958,BMG_DS053738,,NOONAN SYNDROME 7,,,,,,,C3150970,,164757;613706,MONDO:0013379,Noonan syndrome 7,
+BMGC_DS13959,BMG_DS053739,,LEOPARD SYNDROME 3,,,,,DOID:0080550,Noonan syndrome with multiple lentigines 3,C3150971,,164757;613707,MONDO:0013380,LEOPARD syndrome 3,
+BMGC_DS13960,BMG_DS053740,,"NEUROPATHY, HEREDITARY SENSORY, TYPE ID",,,,,DOID:0070156,hereditary sensory neuropathy type 1D,C3150972,,606439;613708,MONDO:0013381,"neuropathy, hereditary sensory, type 1D",
+BMGC_DS13961,BMG_DS053741,771305006,Progressive polyneuropathy with bilateral striatal necrosis,,,,,,,C3150973,,613710,MONDO:0013382,progressive demyelinating neuropathy with bilateral striatal necrosis,Progressive polyneuropathy with bilateral striatal necrosis | Progressive polyneuropathy with bilateral striatal necrosis (disorder)
+BMGC_DS13962,BMG_DS053742,,,,,,,,,C3150974,,613711,MONDO:0013383,"Hirschsprung disease, susceptibility to, 3",
+BMGC_DS13963,BMG_DS053743,,,,,,,,,C3150975,,613712,MONDO:0013384,"Hirschsprung disease, susceptibility to, 4",
+BMGC_DS13964,BMG_DS053744,,TREACHER COLLINS SYNDROME 2,,,,,DOID:0080790,Treacher Collins syndrome 2,C3150983,,613715;613717,MONDO:0013385,Treacher Collins syndrome 2,
+BMGC_DS13965,BMG_DS053745,,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7",,,,,DOID:0080462,developmental and epileptic encephalopathy 7,C3150986,,613720,MONDO:0013387,"developmental and epileptic encephalopathy, 7",
+BMGC_DS13966,BMG_DS053746,,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11",,,,,DOID:0080421,developmental and epileptic encephalopathy 11,C3150987,,613721,MONDO:0013388,"developmental and epileptic encephalopathy, 11",
+BMGC_DS13967,BMG_DS053747,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 12,,,,,DOID:0080459,developmental and epileptic encephalopathy 12,C3150988,,605716;613722;607120,MONDO:0013389,"developmental and epileptic encephalopathy, 12",
+BMGC_DS13968,BMG_DS053748,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q",,,,,,,C3150989,,613723,MONDO:0013390,autosomal recessive limb-girdle muscular dystrophy type 2Q,
+BMGC_DS13969,BMG_DS053749,1296861002,Deficiency of sterol carrier protein X,,,,,,,C3150990,,613724,MONDO:0013391,sterol carrier protein 2 deficiency,SCPX (sterol carrier protein X) deficiency | Sterol carrier protein-2 deficiency | Deficiency of sterol carrier protein X (disorder) | Sterol carrier protein X deficiency | Deficiency of sterol carrier protein X | SCPx (sterol carrier protein x) deficiency
+BMGC_DS13970,BMG_DS053750,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10",,,,,DOID:0050999,autosomal recessive spinocerebellar ataxia 10,C3150998,,613726;613728,MONDO:0013392,autosomal recessive spinocerebellar ataxia 10,
+BMGC_DS13971,BMG_DS053752,,"HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS",,,,,,,C3151000,,606871;613730,MONDO:0013394,porencephaly-microcephaly-bilateral congenital cataract syndrome,
+BMGC_DS13972,BMG_DS053753,,Retinitis Pigmentosa 4,,,,,DOID:0110372,retinitis pigmentosa 4,C3151001,C566706,613731,MONDO:0013395,retinitis pigmentosa 4,
+BMGC_DS13973,BMG_DS053754,,"ACNE INVERSA, FAMILIAL, 2, WITH OR WITHOUT DOWLING-DEGOS DISEASE",,,,,,,C3151037,,613736;607632,MONDO:0013397,"acne inversa, familial, 2",
+BMGC_DS13974,BMG_DS053755,,"ACNE INVERSA, FAMILIAL, 3",,,,,,,C3151038,,104311;613737,MONDO:0013398,"acne inversa, familial, 3",
+BMGC_DS13975,BMG_DS053756,,"Cardiomyopathy, Dilated, 1t",,,,,,,C3151039,C566052,613740,MONDO:0000911,obsolete dilated cardiomyopathy 1T,
+BMGC_DS13976,BMG_DS053757,,"ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE",,,,,DOID:0050546,congenital adrenal insufficiency,C3151055,,118485;613743,MONDO:0013400,"Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency",
+BMGC_DS13977,BMG_DS053758,,"SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE",,,,,DOID:0110803,hereditary spastic paraplegia 51,C3151056,,607244;613744,MONDO:0013401,hereditary spastic paraplegia 51,
+BMGC_DS13978,BMG_DS053759,,"HETEROTAXY, VISCERAL, 4, AUTOSOMAL",,,,,,,C3151057,,602730;613751,MONDO:0013403,"heterotaxy, visceral, 4, autosomal",
+BMGC_DS13979,BMG_DS053760,724040000,S-adenosylhomocysteine hydrolase deficiency,,,,,,,C3151058,,613752,MONDO:0013404,hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase,Deficiency of S-adenosylhomocysteine hydrolase (disorder) | S-adenosylhomocysteine hydrolase deficiency | Deficiency of S-adenosylhomocysteine hydrolase
+BMGC_DS13980,BMG_DS053761,,RETINITIS PIGMENTOSA 49,,,,,,,C3151059,,123825;613756,MONDO:0013405,retinitis pigmentosa 49,
+BMGC_DS13981,BMG_DS053762,,"Macular Degeneration, Age-Related, 6",,,,,,,C3151060,C563674,613757,MONDO:0013406,age related macular degeneration 6,
+BMGC_DS13982,BMG_DS053763,,RETINITIS PIGMENTOSA 47,,,,,,,C3151061,,613758;181031,MONDO:0013407,retinitis pigmentosa 47,
+BMGC_DS13983,BMG_DS053764,,"IMMUNODEFICIENCY 90 WITH ENCEPHALOPATHY, FUNCTIONAL HYPOSPLENIA, AND HEPATIC DYSFUNCTION",,,,,,,C3151062,,613759;602457,MONDO:0013408,FADD-related immunodeficiency,
+BMGC_DS13984,BMG_DS053765,,"MACULAR DEGENERATION, AGE-RELATED, 5",,,,,DOID:0110028,age related macular degeneration 5,C3151063,,613761,MONDO:0013409,age related macular degeneration 5,
+BMGC_DS13985,BMG_DS053766,,"46,XY SEX REVERSAL 6",,,,,DOID:0111769,"46,XY sex reversal 6",C3151064,,600982;613762,MONDO:0013410,"46,XY sex reversal 6",
+BMGC_DS13986,BMG_DS053768,,RETINITIS PIGMENTOSA 45,,,,,,,C3151066,,600724;613767,MONDO:0013413,retinitis pigmentosa 45,
+BMGC_DS13987,BMG_DS053769,,RETINITIS PIGMENTOSA 44,,,,,,,C3151068,,600342;613769,MONDO:0013414,retinitis pigmentosa 44,
+BMGC_DS13988,BMG_DS053770,,CHROMOSOME 17p13.1 DELETION SYNDROME,,,,,,,C3151069,,613776,MONDO:0013415,chromosome 17p13.1 deletion syndrome,
+BMGC_DS13989,BMG_DS053771,,"MACULAR DEGENERATION, AGE-RELATED, 8",,,,,DOID:0110020,age related macular degeneration 8,C3151070,,613778,MONDO:0013416,age related macular degeneration 8,
+BMGC_DS13990,BMG_DS053772,,"COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE",,,,,,,C3151071,,613779,MONDO:0013417,complement component 3 deficiency,
+BMGC_DS13991,BMG_DS053773,,"AORTIC ANEURYSM, FAMILIAL THORACIC 7",,,,,,,C3151077,,613780;600922,MONDO:0013418,"aortic aneurysm, familial thoracic 7",
+BMGC_DS13992,BMG_DS053774,,Complement Component C1s Deficiency,,,,,,,C3151078,C565170,613783,MONDO:0013419,complement component C1s deficiency,
+BMGC_DS13993,BMG_DS053775,,"MACULAR DEGENERATION, AGE-RELATED, 12",,,,,DOID:0110024,age related macular degeneration 12,C3151079,,613784,MONDO:0013420,age related macular degeneration 12,
+BMGC_DS13994,BMG_DS053776,,"COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II",,,,,,,C3151080,,613789,MONDO:0013421,type II complement component 8 deficiency,
+BMGC_DS13995,BMG_DS053777,,"COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I",,,,,,,C3151081,,613790,MONDO:0013422,type I complement component 8 deficiency,
+BMGC_DS13996,BMG_DS053778,,MASP2 Deficiency,,,,,,,C3151085,C565360,613791,MONDO:0013423,immunodeficiency due to MASP-2 deficiency,
+BMGC_DS13997,BMG_DS053779,,Retinitis Pigmentosa 20,,,,,DOID:0110353,retinitis pigmentosa 20,C3151086,C566718,613794,MONDO:0013425,retinitis pigmentosa 20,
+BMGC_DS13998,BMG_DS053780,,LOEYS-DIETZ SYNDROME 3,,,,,DOID:0070237,Loeys-Dietz syndrome 3,C3151087,,603109;613795,MONDO:0013426,aneurysm-osteoarthritis syndrome,
+BMGC_DS13999,BMG_DS053781,,IMMUNODEFICIENCY 31B,,,,,DOID:0111944,immunodeficiency 31B,C3151088,,600555;613796,MONDO:0013427,immunodeficiency 31B,
+BMGC_DS14000,BMG_DS053782,,MEIER-GORLIN SYNDROME 2,,,,,DOID:0080513,Meier-Gorlin syndrome 2,C3151097,,613800;603056,MONDO:0013428,Meier-Gorlin syndrome 2,
+BMGC_DS14001,BMG_DS053783,,RETINITIS PIGMENTOSA 40,,,,,,,C3151107,,180072;613801,MONDO:0013429,retinitis pigmentosa 40,
+BMGC_DS14002,BMG_DS053784,,MEIER-GORLIN SYNDROME 3,,,,,DOID:0080514,Meier-Gorlin syndrome 3,C3151113,,607213;613803,MONDO:0013430,Meier-Gorlin syndrome 3,
+BMGC_DS14003,BMG_DS053785,,MEIER-GORLIN SYNDROME 4,,,,,DOID:0080515,Meier-Gorlin syndrome 4,C3151120,,605525;613804,MONDO:0013431,Meier-Gorlin syndrome 4,
+BMGC_DS14004,BMG_DS053786,,MEIER-GORLIN SYNDROME 5,,,,,DOID:0080516,Meier-Gorlin syndrome 5,C3151126,,602627;613805,MONDO:0013432,Meier-Gorlin syndrome 5,
+BMGC_DS14005,BMG_DS053787,,"CILIARY DYSKINESIA, PRIMARY, 14",,,,,,,C3151136,,613798;613807,MONDO:0013434,primary ciliary dyskinesia 14,
+BMGC_DS14006,BMG_DS053788,,"CILIARY DYSKINESIA, PRIMARY, 15",,,,,,,C3151137,,613799;613808,MONDO:0013435,primary ciliary dyskinesia 15,
+BMGC_DS14007,BMG_DS053789,,RETINITIS PIGMENTOSA 39,,,,,,,C3151138,,608400;613809,MONDO:0013436,retinitis pigmentosa 39,
+BMGC_DS14008,BMG_DS053790,,RETINITIS PIGMENTOSA 43,,,,,,,C3151139,,180071;613810,MONDO:0013437,retinitis pigmentosa 43,
+BMGC_DS14009,BMG_DS053791,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 2D",,,,,,,C3151140,,613811;613009,MONDO:0013438,pontocerebellar hypoplasia type 2D,
+BMGC_DS14010,BMG_DS053793,,"Bile Acid Synthesis Defect, Congenital, 3",,,,,DOID:0111070,congenital bile acid synthesis defect 3,C3151147,C566340,613812,MONDO:0013439,congenital bile acid synthesis defect 3,
+BMGC_DS14011,BMG_DS053794,,SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY,,,,,,,C3151185,,613819,MONDO:0013441,asphyxiating thoracic dystrophy 4,
+BMGC_DS14012,BMG_DS053795,,NEPHRONOPHTHISIS 12,,,,,DOID:0111119,nephronophthisis 12,C3151186,,612014;613820,MONDO:0013442,nephronophthisis 12,
+BMGC_DS14013,BMG_DS053796,,SECKEL SYNDROME 5,,,,,DOID:0070012,Seckel syndrome 5,C3151187,,613529;613823,MONDO:0013443,Seckel syndrome 5,
+BMGC_DS14014,BMG_DS053797,,NEPHRONOPHTHISIS 9,,,,,DOID:0111120,nephronophthisis 9,C3151188,,609799;613824,MONDO:0013444,nephronophthisis 9,
+BMGC_DS14015,BMG_DS053798,,C9 Deficiency,,,,,,,C3151189,C565165,613825,MONDO:0013445,complement component 9 deficiency,
+BMGC_DS14016,BMG_DS053799,,RETINITIS PIGMENTOSA 48,,,,,,,C3151190,,602275;613827,MONDO:0013447,retinitis pigmentosa 48,
+BMGC_DS14017,BMG_DS053800,,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 8",,,,,DOID:0111299,generalized epilepsy with febrile seizures plus 8,C3151191,,613828,MONDO:0013448,"generalized epilepsy with febrile seizures plus, type 8",
+BMGC_DS14018,BMG_DS053801,,LEBER CONGENITAL AMAUROSIS 7,,,,,,,C3151192,,602225;613829,MONDO:0013449,Leber congenital amaurosis 7,
+BMGC_DS14019,BMG_DS053802,,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D",,,,,DOID:0110868,congenital stationary night blindness 1D,C3151193,,603617;613830,MONDO:0013450,congenital stationary night blindness 1D,
+BMGC_DS14020,BMG_DS053803,782724001,Multisystemic smooth muscle dysfunction syndrome,,,,,,,C3151201,,613834,MONDO:0013452,multisystemic smooth muscle dysfunction syndrome,Multisystemic smooth muscle dysfunction syndrome (disorder) | Multisystemic smooth muscle dysfunction syndrome
+BMGC_DS14021,BMG_DS053804,,LEBER CONGENITAL AMAUROSIS 8,,,,,,,C3151202,,604210;613835,MONDO:0013453,Leber congenital amaurosis 8,
+BMGC_DS14022,BMG_DS053805,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16",,,,,DOID:0110322,hypertrophic cardiomyopathy 16,C3151204,,613838;605602,MONDO:0013455,hypertrophic cardiomyopathy 16,
+BMGC_DS14023,BMG_DS053806,,Megaloblastic Anemia due to Dihydrofolate Reductase Deficiency,,,,,,,C3151205,C565095,613839,MONDO:0013456,constitutional megaloblastic anemia with severe neurologic disease,
+BMGC_DS14024,BMG_DS053807,,LEBER CONGENITAL AMAUROSIS 15,,,,,,,C3151206,,602280;613843,MONDO:0013457,Leber congenital amaurosis 15,
+BMGC_DS14025,BMG_DS053808,776416004,"Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome",,,,,,,C3151209,,613845,MONDO:0013458,hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome,"Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome | Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome (disorder) | HUPRA syndrome | Hyperuricaemia, pulmonary hypertension, renal failure, alkalosis syndrome"
+BMGC_DS14026,BMG_DS053809,,"OSTEOGENESIS IMPERFECTA, TYPE X",,,,,,,C3151211,,600943;613848,MONDO:0013459,osteogenesis imperfecta type 10,
+BMGC_DS14027,BMG_DS053810,,"OSTEOGENESIS IMPERFECTA, TYPE XI",,,,,,,C3151218,,607063;610968,MONDO:0012592,osteogenesis imperfecta type 11,
+BMGC_DS14028,BMG_DS053811,,FUCOSYLTRANSFERASE 6 DEFICIENCY,,,,,,,C3151219,,136836;613852,MONDO:0013462,fucosyltransferase 6 deficiency,
+BMGC_DS14029,BMG_DS053812,,,,,,,,,C3151221,,613854,MONDO:0013463,"congenital heart defects, multiple types, 6",
+BMGC_DS14030,BMG_DS053813,,OROFACIAL CLEFT 13,,,,,DOID:0080406,orofacial cleft 13,C3151222,,613857,MONDO:0013466,orofacial cleft 13,
+BMGC_DS14031,BMG_DS053814,,FICOLIN 3 DEFICIENCY,,,,,,,C3151226,,613860;604973,MONDO:0013467,immunodeficiency due to ficolin3 deficiency,
+BMGC_DS14032,BMG_DS053815,,RETINITIS PIGMENTOSA 59,,,,,,,C3151227,,613861;608172,MONDO:0013468,retinitis pigmentosa 59,
+BMGC_DS14033,BMG_DS053816,,RETINITIS PIGMENTOSA 38,,,,,,,C3151228,,604705;613862,MONDO:0013469,retinitis pigmentosa 38,
+BMGC_DS14034,BMG_DS053817,,"FEBRILE SEIZURES, FAMILIAL, 3B",,,,,,,C3151229,,613863,MONDO:0800354,"febrile seizures, familial, 3b",
+BMGC_DS14035,BMG_DS053818,,"DEAFNESS, AUTOSOMAL RECESSIVE 61",,,,,,,C3151230,,604943;613865,MONDO:0013471,autosomal recessive nonsyndromic hearing loss 61,
+BMGC_DS14036,BMG_DS053819,,"Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction",,,,,,,C3151237,C563939,613870,MONDO:0013473,"Hirschsprung disease, cardiac defects, and autonomic dysfunction",
+BMGC_DS14037,BMG_DS053820,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17",,,,,DOID:0110323,hypertrophic cardiomyopathy 17,C3151264,,613873,MONDO:0013474,hypertrophic cardiomyopathy 17,
+BMGC_DS14038,BMG_DS053821,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18",,,,,DOID:0110324,hypertrophic cardiomyopathy 18,C3151265,,172405;613874,MONDO:0013475,hypertrophic cardiomyopathy 18,
+BMGC_DS14039,BMG_DS053822,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20",,,,,DOID:0110326,hypertrophic cardiomyopathy 20,C3151267,,613876;613121,MONDO:0013477,hypertrophic cardiomyopathy 20,
+BMGC_DS14040,BMG_DS053823,,"CARDIOMYOPATHY, DILATED, 1HH",,,,,,,C3151293,,603883;613881,MONDO:0013479,dilated cardiomyopathy 1HH,
+BMGC_DS14041,BMG_DS053824,,"HYPOMAGNESEMIA 6, RENAL",,,,,,,C3151295,,607803;613882,MONDO:0013480,renal hypomagnesemia 6,
+BMGC_DS14042,BMG_DS053825,,,,,,,,,C3151302,,613884,MONDO:0013481,chromosome 13q14 deletion syndrome,
+BMGC_DS14043,BMG_DS053826,,"Obesity, Hyperphagia, and Developmental Delay",,,,,,,C3151303,C563938,613886,MONDO:0013483,"obesity, hyperphagia, and developmental delay",
+BMGC_DS14044,BMG_DS053827,,CATARACT 36,,,,,DOID:0110247,cataract 36,C3151304,,611258;613887,MONDO:0013484,cataract 36,
+BMGC_DS14045,BMG_DS053828,,SPINOCEREBELLAR ATAXIA 32,,,,,,,C3151343,,613909,MONDO:0013486,spinocerebellar ataxia type 32,
+BMGC_DS14046,BMG_DS053829,,"LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3, WITH OR WITHOUT GLOMERULONEPHRITIS",,,,,,,C3151347,,613913,MONDO:0013488,"lipodystrophy, partial, acquired, with low complement component c3, with or without glomerulonephritis",
+BMGC_DS14047,BMG_DS053830,,"DEAFNESS, AUTOSOMAL RECESSIVE 89",,,,,,,C3151351,,613916;601421,MONDO:0013489,autosomal recessive nonsyndromic hearing loss 89,
+BMGC_DS14048,BMG_DS053831,,MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A,,,,,DOID:0080318,megalencephalic leukoencephalopathy with subcortical cysts 2A,C3151355,,613925;611642,MONDO:0013490,megalencephalic leukoencephalopathy with subcortical cysts 2A,
+BMGC_DS14049,BMG_DS053832,,"MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT",,,,,DOID:0080317,megalencephalic leukoencephalopathy with subcortical cysts 2B,C3151356,,613926;611642,MONDO:0013491,"megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without intellectual disability",
+BMGC_DS14050,BMG_DS053833,,ALOPECIA-INTELLECTUAL DISABILITY SYNDROME 3,,,,,DOID:0080951,alopecia-mental retardation syndrome 3,C3151362,,613930,MONDO:0013492,alopecia-intellectual disability syndrome 3,
+BMGC_DS14051,BMG_DS053834,,"PARASOMNIA, SLEEPWALKING TYPE",,,,,,,C3151363,,613938,MONDO:0100226,"parasomnia, sleepwalking type",
+BMGC_DS14052,BMG_DS053835,,"PARASOMNIA, SLEEP TERRORS TYPE",,,,,,,C3151364,,613938,MONDO:0800355,"parasomnia, sleep terrors type",
+BMGC_DS14053,BMG_DS053836,,,,,,,,,C3151378,,613944,MONDO:0013496,"IgA nephropathy, susceptibility to, 2",
+BMGC_DS14054,BMG_DS053837,,OKT4 EPITOPE DEFICIENCY,,,,,,,C3151379,,613949;186940,MONDO:0013497,Okt4 epitope deficiency,
+BMGC_DS14055,BMG_DS053838,,,,,,,,,C3151380,,613950,MONDO:0013498,schizophrenia 15,
+BMGC_DS14056,BMG_DS053839,,"AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 2",,,,,DOID:0080931,primary localized cutaneous amyloidosis 2,C3151404,,613955;609510,MONDO:0013502,"amyloidosis, primary localized cutaneous, 2",
+BMGC_DS14057,BMG_DS053840,,"CANDIDIASIS, FAMILIAL, 6",,,,,,,C3151405,,613956;606496,MONDO:0013503,"candidiasis, familial, 6",
+BMGC_DS14058,BMG_DS053841,,SPERMATOGENIC FAILURE 8,,,,,DOID:0070169,spermatogenic failure 8,C3151406,,184757;613957,MONDO:0013504,spermatogenic failure 8,
+BMGC_DS14059,BMG_DS053842,,SPERMATOGENIC FAILURE 9,,,,,DOID:0111156,spermatogenic failure 9,C3151407,,613958;613893,MONDO:0013505,spermatogenic failure 9,
+BMGC_DS14060,BMG_DS053843,,SCHIZOPHRENIA 16,,,,,DOID:0070092,schizophrenia 16,C3151408,,613959,MONDO:0013506,schizophrenia 16,
+BMGC_DS14061,BMG_DS053844,,"GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 3",,,,,DOID:0070194,autosomal recessive chronic granulomatous disease 3,C3151409,,601488;613960,MONDO:0013507,"granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3",
+BMGC_DS14062,BMG_DS053845,,"MYOPIA 19, AUTOSOMAL DOMINANT",,,,,,,C3151410,,613969,MONDO:0013508,"myopia 19, autosomal dominant",
+BMGC_DS14063,BMG_DS053846,,,,,,,,,C3151411,,613970,MONDO:0013509,"intellectual disability, autosomal dominant 6",
+BMGC_DS14064,BMG_DS053847,,,,,,,,,C3151417,,613972,MONDO:0013510,"melanoma, cutaneous malignant, susceptibility to, 6",
+BMGC_DS14065,BMG_DS053848,,"CYANOSIS, TRANSIENT NEONATAL",,,,,,,C3151421,,142250;613977,MONDO:0013511,"cyanosis, transient neonatal",
+BMGC_DS14066,BMG_DS053849,,"ATRIAL FIBRILLATION, FAMILIAL, 9",,,,,,,C3151431,,600681;613980,MONDO:0013513,"atrial fibrillation, familial, 9",
+BMGC_DS14067,BMG_DS053850,,HYPOTRICHOSIS 3,,,,,DOID:0110700,hypotrichosis 3,C3151432,,613981;608248,MONDO:0013514,hypotrichosis 3,
+BMGC_DS14068,BMG_DS053851,,"OSTEOGENESIS IMPERFECTA, TYPE XII",,,,,,,C3151433,,606633;613849,MONDO:0013460,osteogenesis imperfecta type 12,
+BMGC_DS14069,BMG_DS053852,,RETINITIS PIGMENTOSA 60,,,,,,,C3151434,,613983;613979,MONDO:0013516,retinitis pigmentosa 60,
+BMGC_DS14070,BMG_DS053853,,"PITUITARY HORMONE DEFICIENCY, COMBINED, 6",,,,,DOID:0061022,combined pituitary hormone deficiency 6,C3151440,,600037;613986,MONDO:0013518,"pituitary hormone deficiency, combined, 6",
+BMGC_DS14071,BMG_DS053854,,"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 2",,,,,DOID:0070017,autosomal recessive dyskeratosis congenita 2,C3151441,,606470;613987,MONDO:0013519,"dyskeratosis congenita, autosomal recessive 2",
+BMGC_DS14072,BMG_DS053855,,,,,,,,,C3151442,,613988,MONDO:0013520,"dyskeratosis congenita, autosomal recessive 3",
+BMGC_DS14073,BMG_DS053856,,"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2",,,,,DOID:0070016,autosomal dominant dyskeratosis congenita 2,C3151443,,187270;613989,MONDO:0013521,"dyskeratosis congenita, autosomal dominant 2",
+BMGC_DS14074,BMG_DS053857,,,,,,,,,C3151444,,,MONDO:0027353,autosomal recessive dyskeratosis congenita 4,
+BMGC_DS14075,BMG_DS053858,,,,,,,,,C3151445,,613990,MONDO:0013522,"dyskeratosis congenita, autosomal dominant 3",
+BMGC_DS14076,BMG_DS053859,773331001,Nestor Guillermo progeria syndrome,,,,,,,C3151446,,614008,MONDO:0013523,Nestor-Guillermo progeria syndrome,Nestor Guillermo progeria syndrome (disorder) | Nestor Guillermo progeria syndrome | NGPS - Nestor Guillermo progeria syndrome
+BMGC_DS14077,BMG_DS053860,,"CILIARY DYSKINESIA, PRIMARY, 16",,,,,,,C3151460,,610062;614017,MONDO:0013525,primary ciliary dyskinesia 16,
+BMGC_DS14078,BMG_DS053861,,LISSENCEPHALY 4 WITH MICROCEPHALY,,,,,DOID:0112235,lissencephaly 4,C3151461,,609449;614019,MONDO:0013527,lissencephaly 4,
+BMGC_DS14079,BMG_DS053862,,,,,,,,,C3151462,,614020,MONDO:0013528,"intellectual disability, autosomal recessive 14",
+BMGC_DS14080,BMG_DS053863,,"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3",,,,,,,C3151463,,614021;617242,MONDO:0013529,catecholaminergic polymorphic ventricular tachycardia 3,
+BMGC_DS14081,BMG_DS053864,,"ATRIAL FIBRILLATION, FAMILIAL, 10",,,,,,,C3151464,,600163;614022,MONDO:0013530,"atrial fibrillation, familial, 10",
+BMGC_DS14082,BMG_DS053865,,PROTEIN Z DEFICIENCY,,,,,,,C3151465,,176895;614024,MONDO:0013532,protein Z deficiency,
+BMGC_DS14083,BMG_DS053866,,,,,,,,,C3151466,,614025,MONDO:0013533,hyperlipidemia due to hepatic triglyceride lipase deficiency,
+BMGC_DS14084,BMG_DS053867,,Apolipoprotein C-III Deficiency,,,,,DOID:0111370,apolipoprotein C-III deficiency,C3151467,C566270,614028,MONDO:0013534,apolipoprotein c-III deficiency,
+BMGC_DS14085,BMG_DS053868,,MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA),,,,,,,C3151476,,245400;611224,MONDO:0009504,mitochondrial DNA depletion syndrome 9,
+BMGC_DS14086,BMG_DS053869,,"HYPERCALCIURIA, CHILDHOOD, SELF-LIMITING",,,,,,,C3151482,,248250;603959,,,
+BMGC_DS14087,BMG_DS053870,,"CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA",,,,,,,C3151493,,248910,MONDO:0009569,Hennekam-Beemer syndrome,
+BMGC_DS14088,BMG_DS053872,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3",,,,,DOID:0111236,congenital muscular dystrophy-dystroglycanopathy type A3,C3151519,,253280;606822,MONDO:0009667,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3",
+BMGC_DS14089,BMG_DS053873,,CONGENITAL MYOPATHY 11,,,,,,,C3151531,,610467;619967,MONDO:0859264,congenital myopathy 11,
+BMGC_DS14090,BMG_DS053874,,"NEPHROTIC SYNDROME, TYPE 4",,,,,DOID:0080383,nephrotic syndrome type 4,C3151568,,607102;256370,MONDO:0009733,"nephrotic syndrome, type 4",
+BMGC_DS14091,BMG_DS053875,,"NYSTAGMUS 8, CONGENITAL, AUTOSOMAL RECESSIVE",,,,,DOID:0111797,autosomal recessive congenital nystagmus,C3151571,,257400;602430,MONDO:0009762,"nystagmus, congenital, autosomal recessive",
+BMGC_DS14092,BMG_DS053876,,"BLOUNT DISEASE, ADOLESCENT",,,,,,,C3151572,,259200,MONDO:0009800,"Blount disease, adolescent",
+BMGC_DS14093,BMG_DS053877,,"ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OF PHALANGES AND METACARPALS/METATARSALS",,,,,DOID:0060764,autosomal recessive Robinow syndrome,C3151609,,268310;602337,,,
+BMGC_DS14094,BMG_DS053878,,"ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY",,,,,DOID:0060764,autosomal recessive Robinow syndrome,C3151610,,268310;602337,,,
+BMGC_DS14095,BMG_DS053879,,ANTERIOR SEGMENT DYSGENESIS 7,,,,,DOID:0080612,anterior segment dysgenesis 7,C3151617,,269400;605158,MONDO:0010015,anterior segment dysgenesis 7,
+BMGC_DS14096,BMG_DS053880,,"ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND IMPAIRED INTELLECTUAL DEVELOPMENT",,,,,,,C3151619,,270500,MONDO:0010040,"ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and intellectual disability",
+BMGC_DS14097,BMG_DS053882,,"NYSTAGMUS 6, CONGENITAL, X-LINKED",,,,,DOID:0111795,congenital nystagmus 6,C3151752,,300808;300814,MONDO:0010435,"nystagmus 6, congenital, X-linked",
+BMGC_DS14098,BMG_DS053883,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6,,,,,DOID:0111502,combined oxidative phosphorylation deficiency 6,C3151753,,300169;300816,MONDO:0010437,severe X-linked mitochondrial encephalomyopathy,
+BMGC_DS14099,BMG_DS053884,773329005,CK syndrome,,,,,DOID:0111898,CK syndrome,C3151781,,300831,MONDO:0010441,CK syndrome,"CK syndrome | X-linked intellectual disability, microcephaly, cortical malformation, thin habitus syndrome | CK syndrome (disorder)"
+BMGC_DS14100,BMG_DS053885,,"46,XX SEX REVERSAL 3",,,,,DOID:0111762,"46,XX sex reversal 3",C3151782,,300833,MONDO:0010442,"46,XX sex reversal 3",
+BMGC_DS14101,BMG_DS053886,,CHROMOSOME Xq26 DELETION SYNDROME,,,,,DOID:0111762,"46,XX sex reversal 3",C3151783,,300833,,,
+BMGC_DS14102,BMG_DS053887,,"MACULAR DEGENERATION, ATROPHIC, X-LINKED",,,,,DOID:0112157,X-linked atrophic macular degeneration,C3151784,,300834;312610,MONDO:0010443,"macular degeneration, X-linked atrophic",
+BMGC_DS14103,BMG_DS053889,,"MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM, AND FACIAL DYSMORPHISM",,,,,,,C3151857,,300845,MONDO:0010448,moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome,
+BMGC_DS14104,BMG_DS053890,,"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED",,,,,,,C3151867,,300265;306955,MONDO:0800321,"congenital heart defects, multiple types, 1, X-linked",
+BMGC_DS14105,BMG_DS053892,,"DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL",,,,,DOID:0111751,mitochondrial nonsyndromic sensorineural deafness,C3151897,,500008;516000;516030;561000;590045;590080;590040,MONDO:0010779,mitochondrial non-syndromic sensorineural hearing loss,
+BMGC_DS14106,BMG_DS053893,,"MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT",,,,,,,C3151898,,500009;590025,MONDO:0010780,mitochondrial myopathy with reversible cytochrome C oxidase deficiency,
+BMGC_DS14107,BMG_DS053895,,"RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA",,,,,,,C3151959,,560000,MONDO:0010798,proximal tubulopathy-diabetes mellitus-cerebellar ataxia syndrome,
+BMGC_DS14108,BMG_DS053898,,D-2-HYDROXYGLUTARIC ACIDURIA 1,,,,,DOID:0111351,D-2-hydroxyglutaric aciduria 1,C3152055,,600721;609186,MONDO:0024554,D-2-hydroxyglutaric aciduria 1,
+BMGC_DS14109,BMG_DS053899,,"EPIPHYSEAL DYSPLASIA, MULTIPLE, 3, WITH MYOPATHY",,,,,DOID:0070304,multiple epiphyseal dysplasia 3,C3152083,,120270;600969,,,
+BMGC_DS14110,BMG_DS053900,,"USH1D/F, CDH23/PCDH15, DIGENIC",,,,,,,C3152102,,601067,,,
+BMGC_DS14111,BMG_DS053901,,LEFT VENTRICULAR NONCOMPACTION 3,,,,,,,C3152137,,605906;601493,,,
+BMGC_DS14112,BMG_DS053902,,"AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE",,,,,DOID:0081136,agammaglobulinemia 1,C3152144,,601495,MONDO:0020729,autosomal recessive agammaglobulinemia 1,
+BMGC_DS14113,BMG_DS053904,,,,,,,,,C3152204,,614456,MONDO:0013759,"melanoma, cutaneous malignant, susceptibility to, 8",
+BMGC_DS14114,BMG_DS053906,,BORNHOLM EYE DISEASE,,,,,,,C3159311,,300843,MONDO:0010446,X-linked cone dysfunction syndrome with myopia,
+BMGC_DS14115,BMG_DS053907,,"SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE",,,,,DOID:0111553,spondyloepiphyseal dysplasia Maroteaux type,C3159322,,605427;184095,MONDO:0008473,"spondyloepimetaphyseal dysplasia, Maroteaux type",
+BMGC_DS14116,BMG_DS053908,,"PARKINSON DISEASE, LATE-ONSET",,,,,DOID:0060892,late onset Parkinson's disease,C3160718,,168600,MONDO:0008199,late-onset Parkinson disease,
+BMGC_DS14117,BMG_DS053909,,,,,,,,,C3160719,,161950,MONDO:0008072,"IgA nephropathy, susceptibility to, 1",
+BMGC_DS14118,BMG_DS053910,,"Cardiomyopathy, Dilated, 1u",,,,,,,C3160720,C566296,613694,MONDO:0013371,dilated cardiomyopathy 1U,
+BMGC_DS14119,BMG_DS053911,,,,,,,DOID:0111907,thrombophilia due to thrombin defect,C3160733,,188050,MONDO:0008559,thrombophilia due to thrombin defect,
+BMGC_DS14120,BMG_DS053912,,"DEAFNESS, AUTOSOMAL DOMINANT 51",,,,,,,C3160736,,613558,MONDO:0013305,autosomal dominant nonsyndromic hearing loss 51,
+BMGC_DS14121,BMG_DS053913,,"FANCONI ANEMIA, COMPLEMENTATION GROUP D2",,,,,DOID:0111083,Fanconi anemia complementation group D2,C3160738,,227646;613984,MONDO:0009214,Fanconi anemia complementation group D2,
+BMGC_DS14122,BMG_DS053914,,"FANCONI ANEMIA, COMPLEMENTATION GROUP E",,,,,DOID:0111084,Fanconi anemia complementation group E,C3160739,,600901;613976,MONDO:0010953,Fanconi anemia complementation group E,
+BMGC_DS14123,BMG_DS053915,,"DEAFNESS, AUTOSOMAL RECESSIVE 85",,,,,,,C3160740,,613392,MONDO:0013250,autosomal recessive nonsyndromic hearing loss 85,
+BMGC_DS14124,BMG_DS053919,450886002,Posterior reversible encephalopathy syndrome,,,,I67.83,,,C3160858,,,,,Posterior reversible encephalopathy syndrome | Posterior reversible encephalopathy syndrome (disorder) | Reversible posterior leukoencephalopathy syndrome | Reversible posterior leucoencephalopathy syndrome
+BMGC_DS14125,BMG_DS053931,328571000119101,Secondary spontaneous pneumothorax,,,,J93.12,,,C3161098,,,,,Secondary spontaneous pneumothorax (disorder) | Secondary spontaneous pneumothorax
+BMGC_DS14126,BMG_DS053938,,,,,,,,,C3161174,,613978,MONDO:0013512,hemoglobin H disease,
+BMGC_DS14127,BMG_DS053939,,Hydrops fetalis due to alpha thalassemia,,3A50.0Z,"Alpha thalassaemia, unspecified",D56.0,DOID:0110031;DOID:0110029;DOID:0110030,alpha thalassemia-X-linked intellectual disability syndrome | hemoglobin H disease | alpha thalassemia-intellectual disability syndrome type 1,C3161175,,,,,
+BMGC_DS14128,BMG_DS053956,68779003,Primary immunoglobulin A nephropathy (disorder),,,,,,,C3161650,,,,,Primary IgA nephropathy | Berger's disease | Focal glomerulonephritis | Primary immunoglobulin A nephropathy | Primary immunoglobulin A nephropathy (disorder)
+BMGC_DS14129,BMG_DS053976,448739000,Recurrent lower respiratory tract infection,,,,,,,C3163798,,,,,Recurrent lower respiratory tract infection (disorder) | Recurrent lower respiratory tract infection
+BMGC_DS14130,BMG_DS053983,449082003,Sepsis caused by Gram negative bacteria,,,,,,,C3163829,,,,,Sepsis caused by Gram negative bacteria (disorder) | Sepsis caused by Gram negative bacteria | Severe sepsis with acute organ dysfunction caused by Gram-negative bacteria
+BMGC_DS14131,BMG_DS054033,448054001,Adult onset autosomal dominant leukodystrophy,,,,,DOID:0060785,adult-onset autosomal dominant demyelinating leukodystrophy,C3164344,,,,,Adult onset autosomal dominant leukodystrophy (disorder) | Adult onset autosomal dominant leucodystrophy | Adult onset autosomal dominant leukodystrophy
+BMGC_DS14132,BMG_DS054035,448812000,Sepsis caused by methicillin resistant Staphylococcus aureus,,,,,,,C3164390,,,,,Sepsis caused by methicillin resistant Staphylococcus aureus (disorder) | Sepsis caused by methicillin resistant Staphylococcus aureus | Severe sepsis with acute organ dysfunction caused by methicillin resistant Staphylococcus aureus
+BMGC_DS14133,BMG_DS054147,,Widespread Chronic Pain,Chronic Pain,,,,,,C3178789,D059350,,,,
+BMGC_DS14134,BMG_DS054149,,Heterotaxy Syndrome,Heterotaxy Syndrome,,,,,,C3178805,D059446,,MONDO:0018677,visceral heterotaxy,
+BMGC_DS14135,BMG_DS054150,,,,,,,,,C3178806,,208530,MONDO:0008832,right atrial isomerism,
+BMGC_DS14136,BMG_DS054155,,Bilateral Slipped Capital Femoral Epiphyses,Slipped Capital Femoral Epiphyses,,,,,,C3178898,D060048,182260,MONDO:0018382,epiphysiolysis of the hip,
+BMGC_DS14137,BMG_DS054156,,Unilateral Slipped Capital Femoral Epiphyses,Slipped Capital Femoral Epiphyses,,,,,,C3178899,D060048,182260,MONDO:0018382,epiphysiolysis of the hip,
+BMGC_DS14138,BMG_DS054167,,Disseminated Fusariosis,Fusariosis,,,,DOID:0050289,fusariosis,C3178973,D060585,,,,
+BMGC_DS14139,BMG_DS054168,,Pulmonary Fusariosis,Fusariosis,,,,DOID:0050289,fusariosis,C3178974,D060585,,,,
+BMGC_DS14140,BMG_DS054173,,GALNS Deficiency,Mucopolysaccharidosis IV,,,,,,C3179194,D009085,,,,
+BMGC_DS14141,BMG_DS054174,,Osteopetrosis Autosomal Dominant Type 2,Osteopetrosis,,,,DOID:0110938,autosomal dominant osteopetrosis 2,C3179239,D010022,166600,MONDO:0008156,autosomal dominant osteopetrosis 2,
+BMGC_DS14142,BMG_DS054175,,Pott's Paraplegia,"Tuberculosis, Spinal",,,,,,C3179450,D014399,,,,
+BMGC_DS14143,BMG_DS054176,,"Niemann-Pick Disease, Type C1","Niemann-Pick Disease, Type C",,,,,,C3179455,D052556,257220,MONDO:0009757,"Niemann-Pick disease, type C1",
+BMGC_DS14144,BMG_DS054180,,Linear Verrucous Epidermal Nevus,"Nevus, Sebaceous of Jadassohn",,,,,,C3179502,D054000,,,,
+BMGC_DS14145,BMG_DS054182,,Microdeletion 15q11.2,,,,,DOID:0060393,chromosome 15q11.2 deletion syndrome,C3180937,C557830,615656,MONDO:0014294,chromosome 15q11.2 deletion syndrome,
+BMGC_DS14146,BMG_DS054183,,Non-Infective Endocarditis,"Endocarditis, Non-Infective",,,,DOID:0060068,nonbacterial thrombotic endocarditis,C3202971,D059905,,,,
+BMGC_DS14147,BMG_DS054185,79674009,Hyperheparinemia,,,,D68.32,,,C3203346,C562723,144050,MONDO:0007752,hyperheparinemia,Hyperheparinemia | Hyperheparinaemia | Hyperheparinemia (disorder)
+BMGC_DS14148,BMG_DS054186,191283001;73975000,Factor II deficiency,,,,,,,C3203356,,,,,Hypoprothrombinemia | Hypoprothrombinaemia | Deficiency of factor II &/or prothrombin | Deficiency of factor II or prothrombin | Factor II deficiency | Deficiency of factor II &/or prothrombin (disorder) | Factor II deficiency | Prothrombin deficiency | Factor II deficiency (disorder)
+BMGC_DS14149,BMG_DS054189,,Axial Spondyloarthritis,Axial Spondyloarthritis,,,,,,C3203547,D000089183,,,,
+BMGC_DS14150,BMG_DS054192,,Precordial Catch Syndrome,Chest Pain,,,,,,C3203733,D002637,,,,
+BMGC_DS14151,BMG_DS054194,,Nonalcoholic Steatohepatitis,Non-alcoholic Fatty Liver Disease,,,,DOID:0080208,metabolic dysfunction-associated steatotic liver disease,C3241937,D065626,,MONDO:0007027,metabolic dysfunction-associated steatohepatitis,
+BMGC_DS14152,BMG_DS054201,44279002,Miliaria crystallina,,EE02.Y,Other specified forms of miliaria,L74.1,DOID:0070321,miliaria crystallina,C3241961,,,MONDO:0024229,miliaria crystallina,Miliaria crystallina | Sudamina | Sweat rash | Miliaria crystallina (disorder)
+BMGC_DS14153,BMG_DS054205,226309007;1913007,Familial renal glucosuria,,,,,DOID:0070613,familial renal glucosuria,C3245525,,233100,MONDO:0009297,familial renal glucosuria,Familial renal glucosuria | Familial renal glucosuria (disorder) | Renal glucosuria | Renal glucosuria (disorder)
+BMGC_DS14154,BMG_DS054214,,MYOTONIC DYSTROPHY 1,,,,,,,C3250443,,605377;160900,MONDO:0008056,myotonic dystrophy type 1,
+BMGC_DS14155,BMG_DS054515,,Lupoid hepatitis NEC,,DB96.0,Autoimmune hepatitis,K75.4,,,C3264460,,,,,
+BMGC_DS14156,BMG_DS054557,,Mixed Astigmatism,Astigmatism,,,,,,C3266021,D001251,,,,
+BMGC_DS14157,BMG_DS054558,,Oblique Astigmatism,Astigmatism,,,,,,C3266022,D001251,,,,
+BMGC_DS14158,BMG_DS054568,,,,,,,,,C3266076,,,MONDO:0000358,orofacial cleft,
+BMGC_DS14159,BMG_DS054592,,Multiple Chronic Conditions,Multiple Chronic Conditions,,,,,,C3266262,D000071069,,,,
+BMGC_DS14160,BMG_DS054609,791000124107,2-methyl-3-hydroxybutyric aciduria,,,,,,,C3266731,,300438;300220,MONDO:0010327,HSD10 mitochondrial disease,2-methyl-3-hydroxybutyric aciduria (disorder) | 2-methyl-3-hydroxybutyric aciduria | HSD10 disease
+BMGC_DS14161,BMG_DS054616,,"Atypical Mycobacteriosis, Familial","Mycobacterium Infections, Nontuberculous",,,,,,C3266863,D009165,,MONDO:0019146,inherited susceptibility to mycobacterial diseases,
+BMGC_DS14162,BMG_DS054618,,Waardenburg Syndrome,Waardenburg Syndrome,,,,DOID:9258,Waardenburg syndrome,C3266898,D014849,,MONDO:0018094,Waardenburg syndrome,
+BMGC_DS14163,BMG_DS054641,,,,,,,,,C3272797,,,MONDO:0100290,colon serrated polyposis,
+BMGC_DS14164,BMG_DS054643,,,,,,,,,C3272802,,,MONDO:0006231,gastrointestinal hamartoma,
+BMGC_DS14165,BMG_DS054649,,,,,,,,,C3272841,,608456,MONDO:0012041,familial adenomatous polyposis 2,
+BMGC_DS14166,BMG_DS054656,,,,,,,DOID:8151,appendiceal L-cell glucagon-like peptide producing tumor,C3274138,,,MONDO:0021101,appendix L-cell glucagon-like peptide-producing neuroendocrine tumor,
+BMGC_DS14167,BMG_DS054657,,,,,,,DOID:7401,colonic L-cell glucagon-like peptide producing tumor,C3274139,,,MONDO:0004210,colonic L-cell glucagon-like peptide producing tumor,
+BMGC_DS14168,BMG_DS054658,,,,,,,DOID:7402,L-cell glucagon-like peptide producing tumor,C3274140,,,MONDO:0004211,L-cell glucagon-like peptide-producing neuroendocrine tumor,
+BMGC_DS14169,BMG_DS054659,,,,,,,DOID:7506,small intestinal L-cell glucagon-like peptide producing tumor,C3274143,,,MONDO:0004252,small intestinal L-cell glucagon-like peptide producing tumor,
+BMGC_DS14170,BMG_DS054663,,"MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS",,,,,,,C3275356,,300422,,,
+BMGC_DS14171,BMG_DS054664,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, RAYMOND TYPE",,,,,,,C3275406,,300646;300799,MONDO:0010427,syndromic X-linked intellectual disability Raymond type,
+BMGC_DS14172,BMG_DS054665,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 96",,,,,DOID:0112035,non-syndromic X-linked intellectual disability 96,C3275408,,313475;300802,MONDO:0010429,"intellectual disability, X-linked 96",
+BMGC_DS14173,BMG_DS054666,,,,,,,,,C3275438,,300847,MONDO:0010449,"autism, susceptibility to, X-linked 5",
+BMGC_DS14174,BMG_DS054667,,,,,,,,,C3275443,,300850,MONDO:0010452,"intellectual disability, X-linked 90",
+BMGC_DS14175,BMG_DS054668,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 88",,,,,DOID:0112053,non-syndromic X-linked intellectual disability 88,C3275444,,300852,MONDO:0010454,"intellectual disability, X-linked 88",
+BMGC_DS14176,BMG_DS054669,711481001,"X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia",,,,,,,C3275445,,300853,MONDO:0010455,"X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia","X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia | X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia (disorder)"
+BMGC_DS14177,BMG_DS054670,,,,,,,,,C3275446,,300854,MONDO:0010456,"renal cell carcinoma, Xp11-associated",
+BMGC_DS14178,BMG_DS054671,771442003,Ogden syndrome,,,,,,,C3275447,,300855,MONDO:0010457,Ogden syndrome,"Premature ageing appearance, developmental delay, cardiac arrhythmia syndrome | Ogden syndrome (disorder) | Ogden syndrome | Premature aging appearance, developmental delay, cardiac arrhythmia syndrome"
+BMGC_DS14179,BMG_DS054673,,AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA,,,,,DOID:0060206,amyotrophic lateral sclerosis type 15,C3275459,,300264;300857,MONDO:0010459,amyotrophic lateral sclerosis type 15,
+BMGC_DS14180,BMG_DS054674,,,,,,,,,C3275460,,300858,MONDO:0010460,syndromic X-linked intellectual disability 17,
+BMGC_DS14181,BMG_DS054675,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE",,,,,,,C3275464,,300860;312180,MONDO:0010461,syndromic X-linked intellectual disability Nascimento type,
+BMGC_DS14182,BMG_DS054676,,,,,,,,,C3275471,,300861,MONDO:0010462,syndromic X-linked intellectual disability Chudley-Schwartz type,
+BMGC_DS14183,BMG_DS054677,,"CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA",,,,,DOID:0112106,"chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia",C3275476,,300272;300863,MONDO:0010463,"X-linked dominant chondrodysplasia, Chassaing-Lacombe type",
+BMGC_DS14184,BMG_DS054678,770604006,"X-linked cerebral, cerebellar, coloboma syndrome",,,,,,,C3275487,,300864,MONDO:0010464,X-linked cerebral-cerebellar-coloboma syndrome syndrome,"X-linked cerebral, cerebellar, coloboma syndrome (disorder) | X-linked intellectual disability Kroes type | X-linked cerebral, cerebellar, coloboma syndrome"
+BMGC_DS14185,BMG_DS054679,,KABUKI SYNDROME 2,,,,,,,C3275495,,300128;300867,MONDO:0010465,Kabuki syndrome 2,
+BMGC_DS14186,BMG_DS054680,,MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2,,,,,DOID:0080139,multiple congenital anomalies-hypotonia-seizures syndrome 2,C3275508,,300868;311770,MONDO:0010466,multiple congenital anomalies-hypotonia-seizures syndrome 2,
+BMGC_DS14187,BMG_DS054681,,CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME,,,,,,,C3275521,,300869,MONDO:0010467,Xq27.3q28 duplication syndrome,
+BMGC_DS14188,BMG_DS054682,,"NAIL DISORDER, NONSYNDROMIC CONGENITAL, 6",,,,,DOID:0080084,nonsyndromic congenital nail disorder 6,C3275544,,107000,MONDO:0007135,nonsyndromic congenital nail disorder 6,
+BMGC_DS14189,BMG_DS054683,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 16",,,,,,,C3275558,,300546;305400,,,
+BMGC_DS14190,BMG_DS054684,,,,,,,,,C3275625,,310980,MONDO:0010696,"omphalocele, X-linked",
+BMGC_DS14191,BMG_DS054686,,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1",,,,,DOID:0111748,mitochondrial complex V (ATP synthase) deficiency mitochondrial type 1,C3275684,,500015;516060,MONDO:0027069,"mitochondrial complex 5 (ATP synthase) deficiency, mitochondrial type 1",
+BMGC_DS14192,BMG_DS054688,,,,,,,,,C3275898,,601331,MONDO:0011037,"renal dysplasia, cystic, susceptibility to",
+BMGC_DS14193,BMG_DS054690,,"LUNG AGENESIS, CONGENITAL HEART DEFECTS, AND THUMB ANOMALIES SYNDROME",,,,,,,C3275954,,601612,MONDO:0011116,lung agenesis-heart defect-thumb anomalies syndrome,
+BMGC_DS14194,BMG_DS054691,,,,,,,,,C3275959,,,MONDO:0100173,"leukemia, acute myeloid, susceptibility to",
+BMGC_DS14195,BMG_DS054693,,THROMBOCYTHEMIA 2,,,,,,,C3275998,,159530;601977,MONDO:0011173,thrombocythemia 2,
+BMGC_DS14196,BMG_DS054695,,ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS,,,,,,,C3276096,,108900,MONDO:0007173,atrial septal defect 7,
+BMGC_DS14197,BMG_DS054696,,"ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2",,,,,,,C3276161,,614473;603234,MONDO:0013768,"arterial calcification, generalized, of infancy, 2",
+BMGC_DS14198,BMG_DS054697,,ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE,,,,,,,C3276228,,101800,MONDO:0007044,Acrodysostosis 1 with or without hormone resistance,
+BMGC_DS14199,BMG_DS054698,,"LONG QT SYNDROME 2/3, DIGENIC",,,,,,,C3276240,,600163;603830;613688;152427,,,
+BMGC_DS14200,BMG_DS054699,,"LONG QT SYNDROME 3/6, DIGENIC",,,,,,,C3276241,,600163;603796;603830;613693,,,
+BMGC_DS14201,BMG_DS054700,,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1",,,,,DOID:0050768,mitochondrial complex V (ATP synthase) deficiency nuclear type 1,C3276276,,604273;608918,MONDO:0011421,"mitochondrial complex V (ATP synthase) deficiency, nuclear type 1",
+BMGC_DS14202,BMG_DS054702,1208485009,Multiple mitochondrial dysfunctions syndrome type 1,,,,,,,C3276432,,605711,MONDO:0011582,multiple mitochondrial dysfunctions syndrome 1,MMDS1 - multiple mitochondrial dysfunctions syndrome type 1 | Multiple mitochondrial dysfunctions syndrome type 1 | Multiple mitochondrial dysfunctions syndrome type 1 (disorder) | NFU1 (NFU1 iron-sulfur cluster scaffold) deficiency
+BMGC_DS14203,BMG_DS054703,,"CUTIS LAXA, AUTOSOMAL DOMINANT 1",,,,,,,C3276539,,130160;123700,MONDO:0007411,"cutis laxa, autosomal dominant 1",
+BMGC_DS14204,BMG_DS054704,,"OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY",,,,,DOID:0111340,dominant optic atrophy plus syndrome,C3276549,,605290;125250,MONDO:0007429,"optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy",
+BMGC_DS14205,BMG_DS054707,,Small Fiber Neuropathy,Small Fiber Neuropathy,,,,,,C3276706,D000071075,,MONDO:0800207,"neuropathy, small fiber",
+BMGC_DS14206,BMG_DS054713,,KOILONYCHIA WITH LEUKONYCHIA,,,,,DOID:0080080,nonsyndromic congenital nail disorder 2,C3276971,,149300,,,
+BMGC_DS14207,BMG_DS054714,,"BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT",,,,,DOID:0111059,Bernard-Soulier syndrome type A2,C3277076,,606672;153670,MONDO:0007930,"Bernard-Soulier syndrome, type A2, autosomal dominant",
+BMGC_DS14208,BMG_DS054715,,CHROMOSOME 2q23.1 DELETION SYNDROME,,,,,DOID:0070031,autosomal dominant intellectual developmental disorder 1,C3277090,,156200,,,
+BMGC_DS14209,BMG_DS054717,,"OMPHALOCELE, AUTOSOMAL",,,,,,,C3277235,,164750,MONDO:0008124,"omphalocele, autosomal",
+BMGC_DS14210,BMG_DS054719,,THROMBOCYTHEMIA 1,,,,,,,C3277671,,600044;187950,MONDO:0008554,thrombocythemia 1,
+BMGC_DS14211,BMG_DS054721,,"LONG QT SYNDROME 1/2, DIGENIC",,,,,,,C3277700,,192500;152427;607542;613688,,,
+BMGC_DS14212,BMG_DS054722,,,,,,,,,C3277701,,193200,MONDO:0700077,vitiligo-associated multiple autoimmune disease susceptibility 6,
+BMGC_DS14213,BMG_DS054723,,JOUBERT SYNDROME 12,,,,,,,C3277723,,200990;611254,,,
+BMGC_DS14214,BMG_DS054724,,"17,20-Lyase Deficiency, Isolated",,,,,,,C3277849,C567076,,MONDO:0800378,"17,20-lyase deficiency, isolated",
+BMGC_DS14215,BMG_DS054725,,"NAIL DISORDER, NONSYNDROMIC CONGENITAL, 4",,,,,,,C3277900,,206800;610573,,,
+BMGC_DS14216,BMG_DS054727,,FIBROCHONDROGENESIS 1,,,,,DOID:0080672,fibrochondrogenesis 1,C3278138,,228520,MONDO:0009226,fibrochondrogenesis 1,
+BMGC_DS14217,BMG_DS054728,,"GALACTOSEMIA, DUARTE VARIANT",,,,,,,C3278146,,230400;606999,,,
+BMGC_DS14218,BMG_DS054729,,GELEOPHYSIC DYSPLASIA 1,,,,,DOID:0111725,geleophysic dysplasia 1,C3278147,,231050;612277,MONDO:0009269,geleophysic dysplasia 1,
+BMGC_DS14219,BMG_DS054730,,"BERNARD-SOULIER SYNDROME, TYPE A1",,,,,,,C3278148,,231200;606672,,,
+BMGC_DS14220,BMG_DS054731,,"GLAUCOMA, PRIMARY OPEN ANGLE, ADULT-ONSET",,,,,,,C3278152,,137760;231300;601771,,,
+BMGC_DS14221,BMG_DS054732,,"GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET",,,,,,,C3278153,,231300;601771,,,
+BMGC_DS14222,BMG_DS054733,,GLUTARIC ACIDEMIA IIA,,,,,,,C3278154,,231680;608053,MONDO:0700073,glutaric acidemia IIa,
+BMGC_DS14223,BMG_DS054734,,GLUTARIC ACIDEMIA IIB,,,,,,,C3278155,,130410;231680,MONDO:0700074,glutaric acidemia IIb,
+BMGC_DS14224,BMG_DS054735,,GLUTARIC ACIDEMIA IIC,,,,,,,C3278156,,231675;231680,MONDO:0700076,glutaric acidemia IIc,
+BMGC_DS14225,BMG_DS054738,,"THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT",,,,,DOID:0111900,autosomal dominant thrombophilia due to protein S deficiency,C3278211,,176880;612336,MONDO:0012868,"thrombophilia due to protein S deficiency, autosomal dominant",
+BMGC_DS14226,BMG_DS054742,,"ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS, FAMILIAL",,,,,,,C3278302,,103920,MONDO:0015243,allergic bronchopulmonary aspergillosis,
+BMGC_DS14227,BMG_DS054745,,HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY,,,,,DOID:0112263,hypoinsulinemic hypoglycemia with hemihypertrophy,C3278384,,240900,MONDO:0009416,hypoinsulinemic hypoglycemia and body hemihypertrophy,
+BMGC_DS14228,BMG_DS054746,,"MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS",,,,,DOID:0080575,Larsen-like syndrome B3GAT3 type,C3278404,,245600,MONDO:0009511,"Larsen-like syndrome, B3GAT3 type",
+BMGC_DS14229,BMG_DS054747,,"MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1",,,,,DOID:0080105,microcephaly and chorioretinopathy 1,C3278481,,251270;610053,MONDO:0009624,microcephaly and chorioretinopathy 1,
+BMGC_DS14230,BMG_DS054749,,OROTIC ACIDURIA WITHOUT MEGALOBLASTIC ANEMIA,,,,,DOID:0050833,orotic aciduria,C3278622,,258900,MONDO:0800308,orotic aciduria without megaloblastic anemia,
+BMGC_DS14231,BMG_DS054750,,"LIVER FAILURE, INFANTILE, TRANSIENT",,,,,DOID:0080778,transient infantile liver failure,C3278664,,613070;610230,MONDO:0013111,acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins,
+BMGC_DS14232,BMG_DS054756,,"LONG QT SYNDROME 2/5, DIGENIC",,,,,,,C3279092,,152427;176261;613688;613695,,,
+BMGC_DS14233,BMG_DS054757,,JOUBERT SYNDROME 11,,,,,DOID:0111119,nephronophthisis 12,C3279203,,613820,MONDO:0800382,Joubert syndrome 11,
+BMGC_DS14234,BMG_DS054763,,HYPOTRICHOSIS 8,,,,,DOID:0110705,hypotrichosis 8,C3279470,,278150;609239,MONDO:0010206,hypotrichosis 8,
+BMGC_DS14235,BMG_DS054764,,Cryptozoospermia,Oligospermia,,,,,,C3279550,D009845,MTHU034825,,,
+BMGC_DS14236,BMG_DS054766,,"HEMOGLOBIN H DISEASE, NONDELETIONAL",,,,,,,C3279561,,141800;141850;613978,,,
+BMGC_DS14237,BMG_DS054767,,"Osteogenesis Imperfecta, Type VI",,,,,,,C3279564,C536047,613982,MONDO:0013515,osteogenesis imperfecta type 6,
+BMGC_DS14238,BMG_DS054768,,,,,,,,,C3279614,,614009,MONDO:0800447,"bleeding disorder, platelet-type, 13, susceptibility to",
+BMGC_DS14239,BMG_DS054770,,Glyoxalase II Deficiency,,,,,,,C3279657,C564215,614033,MONDO:0013535,hydroxyacyl glutathione hydrolase deficiency,
+BMGC_DS14240,BMG_DS054771,,"DEAFNESS, AUTOSOMAL RECESSIVE 29",,,,,,,C3279660,,605608;614035,MONDO:0013537,autosomal recessive nonsyndromic hearing loss 29,
+BMGC_DS14241,BMG_DS054773,,Leukotriene C4 Synthase Deficiency,,,,,,,C3279662,C565439,614037,MONDO:0013539,hypotonia-failure to thrive-microcephaly syndrome,
+BMGC_DS14242,BMG_DS054774,,Emberger Syndrome,GATA2 Deficiency,,,,DOID:0111947,immunodeficiency 21,C3279664,D000077428,614038,MONDO:0013540,deafness-lymphedema-leukemia syndrome,
+BMGC_DS14243,BMG_DS054775,,Perisylvian polymicrogyria,,,,,,,C3279675,,MTHU055355,,,
+BMGC_DS14244,BMG_DS054776,,MOYAMOYA DISEASE 5,,,,,,,C3279690,,614042;102620,MONDO:0013542,Moyamoya disease 5,
+BMGC_DS14245,BMG_DS054777,,"ATRIAL FIBRILLATION, FAMILIAL, 11",,,,,,,C3279693,,614049;121013,MONDO:0013544,"atrial fibrillation, familial, 11",
+BMGC_DS14246,BMG_DS054778,,"ATRIAL FIBRILLATION, FAMILIAL, 12",,,,,,,C3279695,,601439;614050,MONDO:0013545,"atrial fibrillation, familial, 12",
+BMGC_DS14247,BMG_DS054779,,"Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency",,,,,,,C3279699,C567528,614052,MONDO:0013546,mitochondrial complex V (ATP synthase) deficiency nuclear type 2,
+BMGC_DS14248,BMG_DS054780,,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3",,,,,DOID:0060332,mitochondrial complex V (ATP synthase) deficiency nuclear type 3,C3279708,,606153;614053,MONDO:0013547,mitochondrial complex V (ATP synthase) deficiency nuclear type 3,
+BMGC_DS14249,BMG_DS054781,,N-ACETYLASPARTATE DEFICIENCY,,,,,,,C3279716,,610647;614063,MONDO:0013549,N-acetylaspartate deficiency,
+BMGC_DS14250,BMG_DS054782,,"MYOPATHY, DISTAL, 4",,,,,DOID:0111190,distal myopathy 4,C3279722,,102565;614065,MONDO:0013550,distal myopathy with posterior leg and anterior hand involvement,
+BMGC_DS14251,BMG_DS054783,,"SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE",,,,,DOID:0110799,hereditary spastic paraplegia 47,C3279738,,607245;614066,MONDO:0013551,hereditary spastic paraplegia 47,
+BMGC_DS14252,BMG_DS054784,,"SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE",,,,,DOID:0110804,hereditary spastic paraplegia 52,C3279743,,614067;607243,MONDO:0013552,hereditary spastic paraplegia 52,
+BMGC_DS14253,BMG_DS054785,,IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2,,,,,,,C3279748,,614064;614069,MONDO:0013553,immunodeficiency-centromeric instability-facial anomalies syndrome 2,
+BMGC_DS14254,BMG_DS054786,,,,,,,,,C3279754,,614070,MONDO:0013554,"psoriasis 13, susceptibility to",
+BMGC_DS14255,BMG_DS054787,,HERMANSKY-PUDLAK SYNDROME 7,,,,,DOID:0060545,Hermansky-Pudlak syndrome 7,C3279756,,607145;614076,MONDO:0013559,Hermansky-Pudlak syndrome 7,
+BMGC_DS14256,BMG_DS054788,782882009,Chondrodysplasia with joint dislocations gPAPP type,,,,,,,C3279757,,614078,MONDO:0013561,"chondrodysplasia with joint dislocations, gPAPP type",Chondrodysplasia with joint dislocations gPAPP type (disorder) | Chondrodysplasia with joint dislocations gPAPP type
+BMGC_DS14257,BMG_DS054790,,,,,,,,,C3279774,,614079,MONDO:0013562,"aspergillosis, susceptibility to",
+BMGC_DS14258,BMG_DS054791,,,,,,,,,C3279775,,614080,MONDO:0013563,multiple congenital anomalies-hypotonia-seizures syndrome 1,
+BMGC_DS14259,BMG_DS054792,,ANHAPTOGLOBINEMIA,,,,,,,C3279786,,140100;614081,MONDO:0013564,anhaptoglobinemia,
+BMGC_DS14260,BMG_DS054793,,HYPOHAPTOGLOBINEMIA,,,,,,,C3279787,,140100;614081,,,
+BMGC_DS14261,BMG_DS054794,,Atrial Septal Defect 3,,,,,,,C3279790,C563540,614089,MONDO:0013567,atrial septal defect 3,
+BMGC_DS14262,BMG_DS054795,,,,,,,,,C3279791,,614090,MONDO:0013568,"sick sinus syndrome 3, susceptibility to",
+BMGC_DS14263,BMG_DS054796,,SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY,,,,,,,C3279792,,614091,MONDO:0013569,short-rib thoracic dysplasia 7 with or without polydactyly,
+BMGC_DS14264,BMG_DS054797,1220589007,Keppen Lubinsky syndrome,,,,,,,C3279800,,614098,MONDO:0013572,Keppen-Lubinsky syndrome,"Generalized lipodystrophy, progeroid features, severe intellectual disability syndrome | Keppen Lubinsky syndrome (disorder) | Generalised lipodystrophy, progeroid features, severe intellectual disability syndrome | Keppen Lubinsky syndrome"
+BMGC_DS14265,BMG_DS054798,,CRANIOECTODERMAL DYSPLASIA 3,,,,,DOID:0080805,cranioectodermal dysplasia 3,C3279807,,614068;614099,MONDO:0013573,cranioectodermal dysplasia 3,
+BMGC_DS14266,BMG_DS054799,,Kappa-Chain Deficiency,,,,,,,C3279824,C564131,614102,MONDO:0013576,recurrent infections associated with rare immunoglobulin isotypes deficiency,
+BMGC_DS14267,BMG_DS054800,,Methylmalonate Semialdehyde Dehydrogenase Deficiency,,,,,,,C3279840,C566402,614105,MONDO:0013579,methylmalonate semialdehyde dehydrogenase deficiency,
+BMGC_DS14268,BMG_DS054801,,Pyruvate Dehydrogenase E1-Beta Deficiency,,,,,,,C3279841,C566729,614111,MONDO:0013580,pyruvate dehydrogenase E1-beta deficiency,
+BMGC_DS14269,BMG_DS054802,,,,,,,,,C3279842,,614113,MONDO:0013581,"intellectual disability, autosomal dominant 2",
+BMGC_DS14270,BMG_DS054803,,,,,,,,,C3279843,,614114,MONDO:0013582,mosaic variegated aneuploidy syndrome 2,
+BMGC_DS14271,BMG_DS054804,,"CORTICAL MALFORMATIONS, OCCIPITAL",,,,,,,C3279875,,614115;604349,MONDO:0013583,occipital pachygyria and polymicrogyria,
+BMGC_DS14272,BMG_DS054806,,Hereditary Sensory and Autonomic Neuropathy Type Ie,,,,,,,C3279885,C580162,614116,MONDO:0013584,hereditary sensory neuropathy-deafness-dementia syndrome,
+BMGC_DS14273,BMG_DS054807,,,,,,,,,C3279899,,614120,MONDO:0013585,hydrolethalus syndrome 2,
+BMGC_DS14274,BMG_DS054808,,CHITOTRIOSIDASE DEFICIENCY,,,,,,,C3279902,,614122;600031,,,
+BMGC_DS14275,BMG_DS054809,,Lactate Dehydrogenase B Deficiency,,,,,,,C3279904,C563641,614128,MONDO:0013587,glycogen storage disease due to lactate dehydrogenase H-subunit deficiency,
+BMGC_DS14276,BMG_DS054810,,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6,,,,,,,C3279905,,614131;601479,MONDO:0013589,focal segmental glomerulosclerosis 6,
+BMGC_DS14277,BMG_DS054811,,"STICKLER SYNDROME, TYPE IV",,,,,,,C3279941,,120210;614134,MONDO:0013590,"Stickler syndrome, type 4",
+BMGC_DS14278,BMG_DS054812,,"NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9",,,,,DOID:0080087,nonsyndromic congenital nail disorder 9,C3279947,,614149,MONDO:0013592,nonsyndromic congenital nail disorder 9,
+BMGC_DS14279,BMG_DS054813,,"DEAFNESS, AUTOSOMAL DOMINANT 64",,,,,,,C3279948,,605219;614152,MONDO:0013593,autosomal dominant nonsyndromic hearing loss 64,
+BMGC_DS14280,BMG_DS054814,771441005,Hyperbiliverdinemia,,,,,,,C3279964,,614156,MONDO:0013595,hyperbiliverdinemia,Hyperbiliverdinaemia | Hyperbiliverdinemia (disorder) | Hyperbiliverdinemia
+BMGC_DS14281,BMG_DS054815,,"CANDIDIASIS, FAMILIAL, 7",,,,,DOID:0111946,immunodeficiency 31C,C3279990,,614162,MONDO:0013599,autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome,
+BMGC_DS14282,BMG_DS054816,,,,,,,,,C3279991,,614163,MONDO:0800001,"delayed sleep phase syndrome, susceptibility to",
+BMGC_DS14283,BMG_DS054817,,PARAGANGLIOMAS 5,,,,,,,C3279992,,614165,MONDO:0013602,paragangliomas 5,
+BMGC_DS14284,BMG_DS054819,,"MYOPIA 21, AUTOSOMAL DOMINANT",,,,,,,C3279997,,614159;614167,MONDO:0013604,"myopia 21, autosomal dominant",
+BMGC_DS14285,BMG_DS054820,,BRITTLE CORNEA SYNDROME 2,,,,,DOID:0080729,brittle cornea syndrome 2,C3280011,,614161;614170,MONDO:0013605,brittle cornea syndrome 2,
+BMGC_DS14286,BMG_DS054821,,Developmental Dysplasia of the Hip,Developmental Dysplasia of the Hip,,,,DOID:0060930,developmental dysplasia of the hip,C3280020,D000082602,,,,
+BMGC_DS14287,BMG_DS054822,,HERMANSKY-PUDLAK SYNDROME 9,,,,,DOID:0060547,Hermansky-Pudlak syndrome 9,C3280026,,614171;604310,MONDO:0013606,Hermansky-Pudlak syndrome 9,
+BMGC_DS14288,BMG_DS054823,,GATA2 Deficiency,GATA2 Deficiency,,,,DOID:0111947,immunodeficiency 21,C3280030,D000077428,614172,MONDO:0013607,monocytopenia with susceptibility to infections,
+BMGC_DS14289,BMG_DS054824,,JOUBERT SYNDROME 13,,,,,DOID:0110982,Joubert syndrome 13,C3280031,,609863;614173,MONDO:0013608,Joubert syndrome 13,
+BMGC_DS14290,BMG_DS054825,,"MECKEL SYNDROME, TYPE 10",,,,,,,C3280036,,611951;614175,MONDO:0013609,"Meckel syndrome, type 10",
+BMGC_DS14291,BMG_DS054826,,RETINITIS PIGMENTOSA 61,,,,,,,C3280041,,606397;614180,MONDO:0013610,retinitis pigmentosa 61,
+BMGC_DS14292,BMG_DS054827,,RETINITIS PIGMENTOSA 62,,,,,,,C3280042,,154235;614181,MONDO:0013611,retinitis pigmentosa 62,
+BMGC_DS14293,BMG_DS054828,,GELEOPHYSIC DYSPLASIA 2,,,,,DOID:0111726,geleophysic dysplasia 2,C3280054,,134797;614185,MONDO:0013612,geleophysic dysplasia 2,
+BMGC_DS14294,BMG_DS054829,,LEBER CONGENITAL AMAUROSIS 16,,,,,,,C3280062,,614186;603208,MONDO:0013613,Leber congenital amaurosis 16,
+BMGC_DS14295,BMG_DS054830,,CRANIOSYNOSTOSIS AND DENTAL ANOMALIES,,,,,,,C3280073,,614188;600939,MONDO:0013615,craniosynostosis and dental anomalies,
+BMGC_DS14296,BMG_DS054831,,"PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3",,,,,DOID:0070548,primary pigmented nodular adrenocortical disease 3,C3280094,,603390;614190,MONDO:0013616,"pigmented nodular adrenocortical disease, primary, 3",
+BMGC_DS14297,BMG_DS054832,,CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME,,,,,,,C3280099,,605020;614195,MONDO:0013618,craniofacial anomalies and anterior segment dysgenesis syndrome,
+BMGC_DS14298,BMG_DS054833,,"NEPHROTIC SYNDROME, TYPE 6",,,,,DOID:0080384,nephrotic syndrome type 6,C3280100,,600579;614196,MONDO:0013619,"nephrotic syndrome, type 6",
+BMGC_DS14299,BMG_DS054834,,"MYASTHENIC SYNDROME, CONGENITAL, 16",,,,,DOID:0110682,congenital myasthenic syndrome 16,C3280112,,603967;614198,MONDO:0013620,congenital myasthenic syndrome 16,
+BMGC_DS14300,BMG_DS054835,,"NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES",,,,,DOID:0080380,nephrotic syndrome type 5,C3280113,,614199;249660;614199,MONDO:0013621,LAMB2-related infantile-onset nephrotic syndrome,
+BMGC_DS14301,BMG_DS054836,,Glycoprotein IA Deficiency,,,,,,,C3280114,C566000,614200,MONDO:0013622,platelet-type bleeding disorder 9,
+BMGC_DS14302,BMG_DS054837,765977002,Glycoprotein VI deficiency,,,,,,,C3280120,,614201,MONDO:0013623,platelet-type bleeding disorder 11,Bleeding disorder due to glycoprotein VI deficiency (disorder) | Bleeding disorder due to glycoprotein VI deficiency | Glycoprotein VI deficiency | Bleeding disorder platelet-type 11
+BMGC_DS14303,BMG_DS054838,,RAFIQ SYNDROME,,,,,DOID:0081097,Rafiq syndrome,C3280127,,614202;604346,MONDO:0013624,Rafiq syndrome,
+BMGC_DS14304,BMG_DS054839,,PARKINSON DISEASE 17,,,,,DOID:0060897,Parkinson's disease 17,C3280133,,601501;614203,MONDO:0013625,Parkinson disease 17,
+BMGC_DS14305,BMG_DS054840,,THREE M SYNDROME 3,,,,,DOID:0060241,3-M syndrome,C3280146,,614145;614205,MONDO:0013627,3M syndrome 3,
+BMGC_DS14306,BMG_DS054841,,HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 3,,,,,DOID:0070435,hyperphosphatasia with impaired intellectual development syndrome 3,C3280153,,614207;615187,MONDO:0013628,hyperphosphatasia with intellectual disability syndrome 3,
+BMGC_DS14307,BMG_DS054842,,,,,,,,,C3280154,,614208,MONDO:0013629,"intellectual disability, autosomal recessive 16",
+BMGC_DS14308,BMG_DS054843,,"MECKEL SYNDROME, TYPE 9",,,,,,,C3280155,,614144;614209,MONDO:0013630,"Meckel syndrome, type 9",
+BMGC_DS14309,BMG_DS054845,,,,,,,,,C3280160,,614212,MONDO:0013633,"encephalopathy, acute, infection-induced, susceptibility to, 4",
+BMGC_DS14310,BMG_DS054846,,"NEUROPATHY, HEREDITARY SENSORY, TYPE IIC",,,,,DOID:0070147,hereditary sensory neuropathy type 2C,C3280168,,601255;614213,MONDO:0013634,"neuropathy, hereditary sensory, type 2C",
+BMGC_DS14311,BMG_DS054847,,ADAMS-OLIVER SYNDROME 2,,,,,,,C3280182,,614219;614194,MONDO:0013635,Adams-Oliver syndrome 2,
+BMGC_DS14312,BMG_DS054848,,"BILIARY CIRRHOSIS, PRIMARY, 4",,,,,DOID:0070361,primary biliary cholangitis 4,C3280201,,614220,MONDO:0013636,primary biliary cholangitis 4,
+BMGC_DS14313,BMG_DS054849,,"BILIARY CIRRHOSIS, PRIMARY, 5",,,,,DOID:0070362,primary biliary cholangitis 5,C3280202,,614221,MONDO:0013637,primary biliary cholangitis 5,
+BMGC_DS14314,BMG_DS054850,,WARBURG MICRO SYNDROME 3,,,,,,,C3280203,,602207;614222,MONDO:0013638,Warburg micro syndrome 3,
+BMGC_DS14315,BMG_DS054852,,RETINAL ARTERIAL MACROANEURYSM WITH SUPRAVALVULAR PULMONIC STENOSIS,,,,,,,C3280205,,614224,MONDO:0013640,familial retinal arterial macroaneurysm,
+BMGC_DS14316,BMG_DS054854,,WARBURG MICRO SYNDROME 2,,,,,,,C3280214,,609275;614225,MONDO:0013641,Warburg micro syndrome 2,
+BMGC_DS14317,BMG_DS054855,,HOLOPROSENCEPHALY 11,,,,,DOID:0110877,holoprosencephaly 11,C3280215,,608707;614226,MONDO:0013642,holoprosencephaly 11,
+BMGC_DS14318,BMG_DS054856,,"HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3",,,,,,,C3280216,,614227,MONDO:0013643,"hyperuricemic nephropathy, familial juvenile type 3",
+BMGC_DS14319,BMG_DS054857,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O",,,,,,,C3280220,,600112;614228,MONDO:0013644,Charcot-Marie-Tooth disease axonal type 2O,
+BMGC_DS14320,BMG_DS054858,,CHROMOSOME 8q21.11 DELETION SYNDROME,,,,,,,C3280231,,614230,MONDO:0013646,chromosome 8q21.11 deletion syndrome,
+BMGC_DS14321,BMG_DS054859,,"MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME 1",,,,,,,C3280240,,614231;609382,MONDO:0100328,"microcephaly, epilepsy, and diabetes syndrome",
+BMGC_DS14322,BMG_DS054860,,HYPOTRICHOSIS 9,,,,,DOID:0110706,hypotrichosis 9,C3280252,,614237,MONDO:0013649,hypotrichosis 9,
+BMGC_DS14323,BMG_DS054861,,HYPOTRICHOSIS 10,,,,,DOID:0110707,hypotrichosis 10,C3280253,,614238,MONDO:0013650,hypotrichosis 10,
+BMGC_DS14324,BMG_DS054862,,,,,,,,,C3280265,,614249,MONDO:0013651,"intellectual disability, autosomal recessive 18",
+BMGC_DS14325,BMG_DS054863,,NARCOLEPSY 7,,,,,,,C3280266,,614250;159465,MONDO:0013652,narcolepsy 7,
+BMGC_DS14326,BMG_DS054864,,,,,,,,,C3280271,,614251,MONDO:0013653,"Parkinson disease 18, autosomal dominant, susceptibility to",
+BMGC_DS14327,BMG_DS054865,,"ANEURYSM, INTRACRANIAL BERRY, 11",,,,,DOID:0080974,intracranial berry aneurysm 11,C3280275,,614252,MONDO:0013654,"aneurysm, intracranial berry, 11",
+BMGC_DS14328,BMG_DS054866,,"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT",,,,,DOID:0070038,autosomal dominant intellectual developmental disorder 8,C3280282,,614254,MONDO:0013655,"intellectual disability, autosomal dominant 8",
+BMGC_DS14329,BMG_DS054867,,,,,,,DOID:0070039,NESCAV syndrome,C3280283,,,,,
+BMGC_DS14330,BMG_DS054868,,,,,,,,,C3280284,,614256,MONDO:0013657,"intellectual disability, autosomal dominant 10",
+BMGC_DS14331,BMG_DS054869,,CHROMOSOME 20q11-q12 DELETION SYNDROME,,,,,DOID:0070041,autosomal dominant intellectual developmental disorder 11,C3280285,,614257,MONDO:0013658,"intellectual disability, autosomal dominant 11",
+BMGC_DS14332,BMG_DS054870,703369003,Microcephaly-capillary malformation syndrome,,,,,,,C3280296,,614261,MONDO:0013659,microcephaly-capillary malformation syndrome,Microcephaly-capillary malformation syndrome | Microcephaly-capillary malformation syndrome (disorder)
+BMGC_DS14333,BMG_DS054871,,"ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY",,,,,,,C3280309,,609798;614262,MONDO:0013660,"arthrogryposis, Perthes disease, and upward gaze palsy",
+BMGC_DS14334,BMG_DS054872,,Combined Malonic and Methylmalonic Aciduria,,,,,DOID:0111263,combined malonic and methylmalonic acidemia,C3280314,C580002,614265,MONDO:0013661,combined malonic and methylmalonic acidemia,
+BMGC_DS14335,BMG_DS054873,,Platelet-Activating Factor Acetylhydrolase Deficiency,,,,,,,C3280315,C566640,614278,MONDO:0013663,platelet-activating factor acetylhydrolase deficiency,
+BMGC_DS14336,BMG_DS054874,,,,,,,,,C3280332,,614280,MONDO:0013665,"epilepsy, juvenile myoclonic, susceptibility to, 9",
+BMGC_DS14337,BMG_DS054875,,"STICKLER SYNDROME, TYPE V",,,,,,,C3280342,,614284,MONDO:0013666,"Stickler syndrome, type 5",
+BMGC_DS14338,BMG_DS054876,,,,,,,,,C3280345,,614291,MONDO:0013669,"breast-ovarian cancer, familial, susceptibility to, 4",
+BMGC_DS14339,BMG_DS054877,,"MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION",,,,,,,C3280346,,610341;614292,MONDO:0013670,"myopia, high, with cataract and vitreoretinal degeneration",
+BMGC_DS14340,BMG_DS054878,,"HYDATIDIFORM MOLE, RECURRENT, 2",,,,,,,C3280352,,611687;614293,MONDO:0013671,"hydatidiform mole, recurrent, 2",
+BMGC_DS14341,BMG_DS054879,,CHROMOSOME 15q25 DELETION SYNDROME,,,,,DOID:0060396,chromosome 15q25 deletion syndrome,C3280355,,614294,MONDO:0013672,chromosome 15q25 deletion syndrome,
+BMGC_DS14342,BMG_DS054880,,"Wolfram-Like Syndrome, Autosomal Dominant",,,,,,,C3280358,C565631,614296,MONDO:0013673,Wolfram-like syndrome,
+BMGC_DS14343,BMG_DS054881,,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4,,,,,,,C3280371,,614298,MONDO:0013674,neurodegeneration with brain iron accumulation 4,
+BMGC_DS14344,BMG_DS054882,1208486005,Multiple mitochondrial dysfunctions syndrome type 2,,,,,,,C3280378,,614299,MONDO:0013675,multiple mitochondrial dysfunctions syndrome 2,Multiple mitochondrial dysfunctions syndrome type 2 (disorder) | Multiple mitochondrial dysfunctions syndrome type 2 | MMDS2 - multiple mitochondrial dysfunctions syndrome type 2 | BOLA3 (bolA family member 3) deficiency
+BMGC_DS14345,BMG_DS054883,722439009,EDICT syndrome,,,,,,,C3280392,,614303,MONDO:0013678,EDICT syndrome,"Endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning syndrome (disorder) | Endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning syndrome | EDICT syndrome | EDICT (endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning) syndrome | Autosomal dominant keratoconus with early-onset anterior polar cataract | Familial keratoconus with cataract"
+BMGC_DS14346,BMG_DS054885,,SCLEROSTEOSIS 2,,,,,,,C3280402,,604270;614305,MONDO:0013679,sclerosteosis 2,
+BMGC_DS14347,BMG_DS054886,,COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA,,,,,,,C3280415,,600702;614306,MONDO:0013680,cognitive impairment with or without cerebellar ataxia,
+BMGC_DS14348,BMG_DS054887,,Alpha-Methylacyl-CoA Racemase Deficiency,,,,,DOID:0060602,alpha-methylacyl-CoA racemase deficiency,C3280428,C565768,614307,MONDO:0013681,alpha-methylacyl-CoA racemase deficiency,
+BMGC_DS14349,BMG_DS054891,,,,,,,,,C3280442,,614320,MONDO:0013685,"pancreatic cancer, susceptibility to, 4",
+BMGC_DS14350,BMG_DS054892,,"MYOPATHY, DISTAL, TATEYAMA TYPE",,,,,DOID:0111191,distal myopathy Tateyama type,C3280443,,601253;614321,MONDO:0013686,"distal myopathy, Tateyama type",
+BMGC_DS14351,BMG_DS054893,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12",,,,,DOID:0080060,autosomal recessive spinocerebellar ataxia 12,C3280452,,614322;605131,MONDO:0013687,autosomal recessive spinocerebellar ataxia 12,
+BMGC_DS14352,BMG_DS054894,,OVARIAN DYSGENESIS 3,,,,,DOID:0080495,ovarian dysgenesis 3,C3280471,,608665;614324,MONDO:0013689,ovarian dysgenesis 3,
+BMGC_DS14353,BMG_DS054895,,PITT-HOPKINS-LIKE SYNDROME 2,,,,,DOID:0111332,Pitt-Hopkins-like syndrome 2,C3280479,,614325;600565,MONDO:0013690,Pitt-Hopkins-like syndrome 2,
+BMGC_DS14354,BMG_DS054896,,FEINGOLD SYNDROME 2,,,,,,,C3280489,,614326,MONDO:0013691,Feingold syndrome type 2,
+BMGC_DS14355,BMG_DS054897,,TUMOR PREDISPOSITION SYNDROME 1,,,,,,,C3280492,,603089;614327,MONDO:0013692,BAP1-related tumor predisposition syndrome,
+BMGC_DS14356,BMG_DS054898,,"INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 1",,,,,,,C3280501,,603639;614328,MONDO:0013693,"inflammatory skin and bowel disease, neonatal, 1",
+BMGC_DS14357,BMG_DS054899,,,,,,,,,C3280523,,614329,MONDO:0013694,"intellectual disability, autosomal recessive 31",
+BMGC_DS14358,BMG_DS054900,,SCHIZOPHRENIA 17,,,,,,,C3280524,,614332,MONDO:0800358,schizophrenia 17,
+BMGC_DS14359,BMG_DS054901,,,,,,,,,C3280525,,614333,MONDO:0013697,"intellectual disability, autosomal recessive 29",
+BMGC_DS14360,BMG_DS054902,,"ARTHROGRYPOSIS, DISTAL, TYPE 1B",,,,,DOID:0111598,distal arthrogryposis type 1B,C3280526,,160794;614335,MONDO:0013698,"arthrogryposis, distal, type 1B",
+BMGC_DS14361,BMG_DS054903,,,,,,,,,C3280527,,614338,MONDO:0013700,pancreatic triacylglycerol lipase deficiency,
+BMGC_DS14362,BMG_DS054904,,"COLIPASE, CONGENITAL ABSENCE OF PANCREATIC",,,,,,,C3280528,,614338,,,
+BMGC_DS14363,BMG_DS054905,,"LIPASE AND COLIPASE, DEFICIENCY OF",,,,,,,C3280529,,614338,,,
+BMGC_DS14364,BMG_DS054906,,"LIPASE AND COLIPASE, CONGENITAL ABSENCE OF PANCREATIC",,,,,,,C3280530,,614338,,,
+BMGC_DS14365,BMG_DS054907,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 27",,,,,DOID:0081193,autosomal recessive intellectual developmental disorder 27,C3280538,,614340;610350,MONDO:0013702,"intellectual disability, autosomal recessive 27",
+BMGC_DS14366,BMG_DS054908,,,,,,,,,C3280539,,614341,MONDO:0013703,"intellectual disability, autosomal recessive 33",
+BMGC_DS14367,BMG_DS054909,,,,,,,,,C3280540,,614342,MONDO:0013704,"intellectual disability, autosomal recessive 30",
+BMGC_DS14368,BMG_DS054910,,,,,,,,,C3280541,,614343,MONDO:0013705,"intellectual disability, autosomal recessive 19",
+BMGC_DS14369,BMG_DS054911,,,,,,,,,C3280542,,614344,MONDO:0013706,"intellectual disability, autosomal recessive 23",
+BMGC_DS14370,BMG_DS054912,,,,,,,,,C3280543,,614345,MONDO:0013707,"intellectual disability, autosomal recessive 24",
+BMGC_DS14371,BMG_DS054913,,,,,,,,,C3280544,,614346,MONDO:0013708,"intellectual disability, autosomal recessive 25",
+BMGC_DS14372,BMG_DS054914,,,,,,,,,C3280545,,614347,MONDO:0013709,"intellectual disability, autosomal recessive 28",
+BMGC_DS14373,BMG_DS054915,,"PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS",,,,,,,C3280556,,608568;614369,MONDO:0013711,peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome,
+BMGC_DS14374,BMG_DS054916,,"SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 5",,,,,,,C3280574,,138981;614370,MONDO:0013712,"surfactant metabolism dysfunction, pulmonary, 5",
+BMGC_DS14375,BMG_DS054917,,,,,,,,,C3280582,,614371,MONDO:0013713,"dengue virus, susceptibility to",
+BMGC_DS14376,BMG_DS054920,,Mannose-Binding Protein Deficiency,,,,,,,C3280586,C563602,614372,MONDO:0013714,mannose-binding lectin deficiency,
+BMGC_DS14377,BMG_DS054921,,"AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE",,,,,DOID:0060207,amyotrophic lateral sclerosis type 16,C3280587,,601978;614373,MONDO:0013715,amyotrophic lateral sclerosis type 16,
+BMGC_DS14378,BMG_DS054923,,SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY,,,,,,,C3280598,,614376,MONDO:0013717,asphyxiating thoracic dystrophy 5,
+BMGC_DS14379,BMG_DS054924,,NEPHRONOPHTHISIS 13,,,,,DOID:0111121,nephronophthisis 13,C3280612,,608151;614377,MONDO:0013718,nephronophthisis 13,
+BMGC_DS14380,BMG_DS054925,,CRANIOECTODERMAL DYSPLASIA 4,,,,,DOID:0080806,cranioectodermal dysplasia 4,C3280616,,614378;608151,MONDO:0013719,cranioectodermal dysplasia 4,
+BMGC_DS14381,BMG_DS054929,,,,,,,,,C3280641,,614379,MONDO:0013720,complement component 4b deficiency,
+BMGC_DS14382,BMG_DS054930,,,,,,,,,C3280642,,614380,MONDO:0013721,complement component 4a deficiency,
+BMGC_DS14383,BMG_DS054931,,"LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM",,,,,,,C3280644,,614381;213002;614381,MONDO:0013722,hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism,
+BMGC_DS14384,BMG_DS054932,,,,,,,,,C3280645,,614382,MONDO:0013723,"bacteremia, susceptibility to, 1",
+BMGC_DS14385,BMG_DS054933,,,,,,,,,C3280646,,,MONDO:0000108,"bacteremia, susceptibility",
+BMGC_DS14386,BMG_DS054934,,,,,,,,,C3280647,,614383,MONDO:0013724,"bacteremia, susceptibility to, 2",
+BMGC_DS14387,BMG_DS054935,,ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1,,,,,DOID:0070347,encephalopathy due to defective mitochondrial and peroxisomal fission 1,C3280660,,603850;614388,MONDO:0013726,"encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1",
+BMGC_DS14388,BMG_DS054936,,,,,,,,,C3280670,,614389,MONDO:0013727,"pregnancy loss, recurrent, susceptibility to, 1",
+BMGC_DS14389,BMG_DS054937,,,,,,,,,C3280672,,614390,MONDO:0013728,"pregnancy loss, recurrent, susceptibility to, 2",
+BMGC_DS14390,BMG_DS054938,,,,,,,,,C3280674,,614391,MONDO:0013729,"pregnancy loss, recurrent, susceptibility to, 3",
+BMGC_DS14391,BMG_DS054939,,,,,,,,,C3280677,,614395,MONDO:0100048,"graft-versus-host disease, susceptibility to",
+BMGC_DS14392,BMG_DS054940,1236844002,"Early-onset myopathy, areflexia, respiratory distress, dysphagia syndrome",,,,,,,C3280679,,614399,MONDO:0013731,MEGF10-related myopathy,"Early-onset myopathy, areflexia, respiratory distress, dysphagia syndrome (disorder) | EMARDD (early-onset myopathy, areflexia, respiratory distress, dysphagia) syndrome | Early-onset myopathy, areflexia, respiratory distress, dysphagia syndrome"
+BMGC_DS14393,BMG_DS054941,,,,,,,,,C3280689,,614400,MONDO:0013732,"glucocorticoid therapy, response to",
+BMGC_DS14394,BMG_DS054942,764732004,"Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome",,,,,,,C3280692,,614407,MONDO:0013735,microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome,"Zaki Gleeson syndrome | Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome | Microcephaly, cerebellar hypoplasia, congenital heart conduction defect syndrome | Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome (disorder)"
+BMGC_DS14395,BMG_DS054943,,CHILBLAIN LUPUS 2,,,,,,,C3280721,,614415;606754,MONDO:0013739,chilblain lupus 2,
+BMGC_DS14396,BMG_DS054945,,RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES,,,,,,,C3280729,,605207;614416,MONDO:0013740,lethal occipital encephalocele-skeletal dysplasia syndrome,
+BMGC_DS14397,BMG_DS054946,,"EPILEPSY, FAMILIAL TEMPORAL LOBE, 5",,,,,DOID:0060752,familial temporal lobe epilepsy 5,C3280730,,614417;609562,MONDO:0013741,familial temporal lobe epilepsy 5,
+BMGC_DS14398,BMG_DS054947,,"FEBRILE SEIZURES, FAMILIAL, 11",,,,,DOID:0111308,familial febrile seizures 11,C3280734,,614418;609562,MONDO:0024566,"febrile seizures, familial, 11",
+BMGC_DS14399,BMG_DS054948,,SYSTEMIC LUPUS ERYTHEMATOSUS 16,,,,,,,C3280742,,614420;602244,MONDO:0013743,autosomal systemic lupus erythematosus type 16,
+BMGC_DS14400,BMG_DS054950,,CATARACT 37,,,,,,,C3280758,,614422,MONDO:0013744,cataract 37,
+BMGC_DS14401,BMG_DS054951,,JOUBERT SYNDROME 14,,,,,DOID:0110983,Joubert syndrome 14,C3280766,,614424;614423,MONDO:0013745,Joubert syndrome 14,
+BMGC_DS14402,BMG_DS054952,,VENTRICULAR SEPTAL DEFECT 1,,,,,,,C3280777,,614429;600576,MONDO:0013746,ventricular septal defect 1,
+BMGC_DS14403,BMG_DS054954,,ATRIOVENTRICULAR SEPTAL DEFECT 4,,,,,,,C3280781,,600576;614430,MONDO:0013747,atrioventricular septal defect 4,
+BMGC_DS14404,BMG_DS054956,,,,,,,,,C3280783,,614431,MONDO:0013748,ventricular septal defect 2,
+BMGC_DS14405,BMG_DS054957,,VENTRICULAR SEPTAL DEFECT 3,,,,,,,C3280785,,600584;614432,MONDO:0013749,ventricular septal defect 3,
+BMGC_DS14406,BMG_DS054959,,,,,,,,,C3280790,,614433,MONDO:0013750,atrial septal defect 8,
+BMGC_DS14407,BMG_DS054961,,"CUTIS LAXA, AUTOSOMAL DOMINANT 2",,,,,,,C3280794,,604580;614434,MONDO:0013751,"cutis laxa, autosomal dominant 2",
+BMGC_DS14408,BMG_DS054962,,HYPOPLASTIC LEFT HEART SYNDROME 2,,,,,,,C3280795,,614435;600584,MONDO:0013752,hypoplastic left heart syndrome 2,
+BMGC_DS14409,BMG_DS054963,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P",,,,,,,C3280797,,614436;610933;614436;608591,MONDO:0013753,Charcot-Marie-Tooth disease axonal type 2P,
+BMGC_DS14410,BMG_DS054964,,"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB",,,,,,,C3280798,,604633;614437,MONDO:0013754,"cutis laxa, autosomal recessive, type 1B",
+BMGC_DS14411,BMG_DS054965,1295488006,Pyrroline-5-carboxylate reductase 1 related de Barsy syndrome,,,,,,,C3280799,,614438,MONDO:0013755,PYCR1-related de Barsy syndrome,Pyrroline-5-carboxylate reductase 1 related de Barsy syndrome | Disorder due to pyrroline-5-carboxylate reductase 1 deficiency | PYCR1-related de Barsy syndrome | Pyrroline-5-carboxylate reductase 1 related de Barsy syndrome (disorder) | Autosomal recessive cutis laxa type IIIb
+BMGC_DS14412,BMG_DS054966,,"HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2",,,,,,,C3280800,,614441,MONDO:0013756,"hypertrophic osteoarthropathy, primary, autosomal recessive, 2",
+BMGC_DS14413,BMG_DS054967,,"HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6",,,,,,,C3280817,,190120;614450,MONDO:0013757,congenital nongoitrous hypothyroidism 6,
+BMGC_DS14414,BMG_DS054968,1208936008,"Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome",,,,,,,C3280856,,614457,MONDO:0013760,congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome,"ELOVL4 (elongation of very long chain fatty acids-like 4) related neuro ichthyosis | Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome (disorder) | Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome | ELOVL4-related neuro ichthyosis"
+BMGC_DS14415,BMG_DS054969,,THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE),,,,,,,C3280866,,606370;614458,MONDO:0013761,childhood encephalopathy due to thiamine pyrophosphokinase deficiency,
+BMGC_DS14416,BMG_DS054970,,"HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES",,,,,,,C3280887,,607031;614462,MONDO:0013762,lipoic acid synthetase deficiency,
+BMGC_DS14417,BMG_DS054971,,JOUBERT SYNDROME 15,,,,,DOID:0110984,Joubert syndrome 15,C3280897,,610523;614464,MONDO:0013763,Joubert syndrome 15,
+BMGC_DS14418,BMG_DS054972,,"JOUBERT SYNDROME 9/15, DIGENIC",,,,,DOID:0110984,Joubert syndrome 15,C3280898,,612013;612285;614464;610523,,,
+BMGC_DS14419,BMG_DS054973,,"JOUBERT SYNDROME 12/15, DIGENIC",,,,,DOID:0110984,Joubert syndrome 15,C3280899,,200990;610523;611254;614464,,,
+BMGC_DS14420,BMG_DS054974,,JOUBERT SYNDROME 16,,,,,DOID:0110985,Joubert syndrome 16,C3280906,,614459;614465,MONDO:0013764,Joubert syndrome 16,
+BMGC_DS14421,BMG_DS054975,,,,,,,,,C3280913,,614466,MONDO:0013765,"coronary heart disease, susceptibility to, 6",
+BMGC_DS14422,BMG_DS054976,,FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3,,,,,,,C3280914,,600220;614468,MONDO:0013766,familial cold autoinflammatory syndrome 3,
+BMGC_DS14423,BMG_DS054977,,ATRIOVENTRICULAR SEPTAL DEFECT 5,,,,,,,C3280939,,601656;614474,MONDO:0013769,atrioventricular septal defect 5,
+BMGC_DS14424,BMG_DS054978,,ATRIAL SEPTAL DEFECT 9,,,,,,,C3280943,,614475;601656,MONDO:0013770,atrial septal defect 9,
+BMGC_DS14425,BMG_DS054979,,"HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE",,,,,,,C3280953,,138420;614480,MONDO:0013771,transient infantile hypertriglyceridemia and hepatosteatosis,
+BMGC_DS14426,BMG_DS054980,,BRAIN SMALL VESSEL DISEASE 2,,,,,DOID:0112314,brain small vessel disease 2,C3280970,,120090;614483,MONDO:0013773,porencephaly 2,
+BMGC_DS14427,BMG_DS054981,,,,,,,,,C3280974,,614485,MONDO:0013774,trigonocephaly 2,
+BMGC_DS14428,BMG_DS054982,,Thrombophilia due to Thrombomodulin Defect,,,,,DOID:0111908,thrombophilia due to thrombomodulin defect,C3280976,C566057,614486,MONDO:0013775,thrombomodulin-related bleeding disorder,
+BMGC_DS14429,BMG_DS054983,,"SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE",,,,,DOID:0050944,spastic ataxia 5,C3280977,,604581;614487,MONDO:0013776,spastic ataxia 5,
+BMGC_DS14430,BMG_DS054985,,WISKOTT-ALDRICH SYNDROME 2,,,,,,,C3281001,,602357;614493;277970;614493,MONDO:0013779,Wiskott-Aldrich syndrome 2,
+BMGC_DS14431,BMG_DS054986,,RETINITIS PIGMENTOSA 63,,,,,,,C3281002,,614494,MONDO:0013780,retinitis pigmentosa 63,
+BMGC_DS14432,BMG_DS054987,,MICROPHTHALMIA/COLOBOMA 7,,,,,,,C3281027,,605452;614497,MONDO:0013783,"microphthalmia, isolated, with coloboma 7",
+BMGC_DS14433,BMG_DS054988,1197587003,"Lethal neonatal spasticity, epileptic encephalopathy syndrome",,,,,,,C3281029,,614498,MONDO:0013784,neonatal-onset encephalopathy with rigidity and seizures,"Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder) | Lethal neonatal spasticity, epileptic encephalopathy syndrome | Lethal neonatal rigidity, multifocal seizure syndrome"
+BMGC_DS14434,BMG_DS054989,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY",,,,,DOID:0081200,autosomal recessive intellectual developmental disorder 34,C3281044,,603454;614499,MONDO:0013785,"intellectual disability, autosomal recessive 34",
+BMGC_DS14435,BMG_DS054990,,CONE-ROD DYSTROPHY 16,,,,,DOID:0111022,cone-rod dystrophy 16,C3281045,,614477;614500,MONDO:0013786,cone-rod dystrophy 16,
+BMGC_DS14436,BMG_DS054991,,RETINITIS PIGMENTOSA 64,,,,,DOID:0111022,cone-rod dystrophy 16,C3281046,,614477;614500,MONDO:0800359,retinitis pigmentosa 64,
+BMGC_DS14437,BMG_DS054992,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, CRANIOFACIAL ABNORMALITIES, AND SEIZURES",,,,,,,C3281055,,608241;614501,MONDO:0013787,"psychomotor retardation, epilepsy, and craniofacial dysmorphism",
+BMGC_DS14438,BMG_DS054993,,"USHER SYNDROME, TYPE IIIB",,,,,,,C3281066,,142810;614504,MONDO:0013788,Usher syndrome type 3B,
+BMGC_DS14439,BMG_DS054994,733083006,Congenital disorder of glycosylation type 1r,,,,,,,C3281084,,614507,MONDO:0013789,DDOST-congenital disorder of glycosylation,Dolichyl-diphosphooligosaccharide-protein glycosyltransferase congenital disorder of glycosylation | Congenital disorder of glycosylation type Ir | DDOST-CDG - dolichyl-diphosphooligosaccharide-protein glycosyltransferase congenital disorder of glycosylation | Congenital disorder of glycosylation type 1r (disorder) | Congenital disorder of glycosylation type 1r | Carbohydrate deficient glycoprotein syndrome type Ir
+BMGC_DS14440,BMG_DS054995,,MIRROR MOVEMENTS 2,,,,,,,C3281089,,179617;614508,MONDO:0013790,mirror movements 2,
+BMGC_DS14441,BMG_DS054996,,"THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE",,,,,DOID:0111905,autosomal recessive thrombophilia due to protein S deficiency,C3281092,,176880;614514,MONDO:0013791,"thrombophilia due to protein S deficiency, autosomal recessive",
+BMGC_DS14442,BMG_DS054997,,,,,,,,,C3281105,,614519,MONDO:0100533,"hemorrhage, intracerebral, susceptibility to",
+BMGC_DS14443,BMG_DS054998,,"ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY",,,,,,,C3281106,,614520,MONDO:0013793,"encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency",
+BMGC_DS14444,BMG_DS055000,,THROMBOCYTHEMIA 3,,,,,,,C3281125,,614521;147796,MONDO:0013794,thrombocythemia 3,
+BMGC_DS14445,BMG_DS055001,,FIBROCHONDROGENESIS 2,,,,,DOID:0080673,fibrochondrogenesis 2,C3281128,,614524;120290,MONDO:0013795,fibrochondrogenesis 2,
+BMGC_DS14446,BMG_DS055002,764435003,17q12 microduplication syndrome,,,,,,,C3281137,,614526,MONDO:0013796,chromosome 17q12 duplication syndrome,Chromosome 17q12 duplication syndrome | 17q12 duplication syndrome | 17q12 microduplication syndrome | 17q12 microduplication syndrome (disorder) | Trisomy 17q12
+BMGC_DS14447,BMG_DS055003,,CHROMOSOME 17q12 DELETION SYNDROME,,,,,,,C3281138,,614527,MONDO:0013797,chromosome 17q12 deletion syndrome,
+BMGC_DS14448,BMG_DS055004,,CHROMOSOME 16q22 DELETION SYNDROME,,,,,DOID:0060401,chromosome 16q22 deletion syndrome,C3281152,,614541,MONDO:0013798,chromosome 16q22 deletion syndrome,
+BMGC_DS14449,BMG_DS055005,,,,,,,,,C3281153,,,MONDO:0800431,"efavirenz central nervous system toxicity, susceptibility to",
+BMGC_DS14450,BMG_DS055006,,"EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2",,,,,DOID:0080735,Ehlers-Danlos syndrome kyphoscoliotic type 2,C3281160,,614505;614557,MONDO:0013800,"Ehlers-Danlos syndrome, kyphoscoliotic type, 2",
+BMGC_DS14451,BMG_DS055008,765170001,SCN8A-related epilepsy with encephalopathy,,,,,,,C3281191,,614558,MONDO:0013801,"developmental and epileptic encephalopathy, 13",SCN8A encephalopathy | SCN8A (sodium voltage-gated channel alpha subunit 8) related epilepsy with encephalopathy | Early infantile epileptic encephalopathy 13 | Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy (disorder) | SCN8A-related epilepsy with encephalopathy | Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy
+BMGC_DS14452,BMG_DS055009,782822006,Infantile cerebellar and retinal degeneration,,,,,,,C3281192,,614559,MONDO:0013802,infantile cerebellar-retinal degeneration,Infantile cerebellar and retinal degeneration (disorder) | Infantile cerebellar and retinal degeneration
+BMGC_DS14453,BMG_DS055010,,Leukoencephalopathy Brain Calcifications and Cysts,,,,,,,C3281200,C000598644,614561,MONDO:0013803,leukoencephalopathy with calcifications and cysts,
+BMGC_DS14454,BMG_DS055011,,COFFIN-SIRIS SYNDROME 1,,,,,DOID:0070042,Coffin-Siris syndrome 1,C3281201,,135900;135900;609943;614562;614556,MONDO:0007617,Coffin-Siris syndrome 1,
+BMGC_DS14455,BMG_DS055012,,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 13",,,,,DOID:0070043,autosomal dominant intellectual developmental disorder 13,C3281202,,600112;614563,MONDO:0013805,"intellectual disability, autosomal dominant 13",
+BMGC_DS14456,BMG_DS055013,,,,,,,,,C3281203,,614564,MONDO:0013806,familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome,
+BMGC_DS14457,BMG_DS055014,,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E",,,,,DOID:0110869,congenital stationary night blindness 1E,C3281215,,614515;614565,MONDO:0013807,congenital stationary night blindness 1E,
+BMGC_DS14458,BMG_DS055016,,"CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME",,,,,,,C3281223,,102579;614575,MONDO:0044720,cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome,
+BMGC_DS14459,BMG_DS055017,,BARAITSER-WINTER SYNDROME 2,,,,,DOID:0081113,Baraitser-Winter syndrome 2,C3281235,,102560;614583,MONDO:0013812,Baraitser-winter syndrome 2,
+BMGC_DS14460,BMG_DS055018,,DYSTONIA 21,,,,,,,C3281236,,614588,MONDO:0013813,dystonia 21,
+BMGC_DS14461,BMG_DS055020,,BENT BONE DYSPLASIA SYNDROME 1,,,,,DOID:0060992,bent bone dysplasia syndrome 1,C3281247,,176943;614592,MONDO:0013815,bent bone dysplasia syndrome 1,
+BMGC_DS14462,BMG_DS055027,,PREECLAMPSIA/ECLAMPSIA 5,,,,,,,C3281288,,605236;614595,MONDO:0013817,preeclampsia/eclampsia 5,
+BMGC_DS14463,BMG_DS055028,,TRICHOHEPATOENTERIC SYNDROME 2,,,,,DOID:0111416,trichohepatoenteric syndrome 2,C3281289,,600478;614602,MONDO:0013818,trichohepatoenteric syndrome 2,
+BMGC_DS14464,BMG_DS055029,,"DEAFNESS, AUTOSOMAL DOMINANT 4B",,,,,,,C3281297,,614614;614591,MONDO:0013823,autosomal dominant nonsyndromic hearing loss 4B,
+BMGC_DS14465,BMG_DS055032,,,,,,,,,C3463824,,614286,MONDO:0018881,myelodysplastic syndrome,
+BMGC_DS14466,BMG_DS055033,,"HYDATIDIFORM MOLE, RECURRENT, 1",,,,,,,C3463897,,609661;231090,MONDO:0009273,"hydatidiform mole, recurrent, 1",
+BMGC_DS14467,BMG_DS055035,,Complement Factor I Deficiency,,,,,DOID:0050419,complement factor I deficiency,C3463916,C572568,610984,MONDO:0012594,complement factor I deficiency,
+BMGC_DS14468,BMG_DS055036,,,,,,,,,C3463917,,610600,MONDO:0012524,corticosterone methyloxidase type 2 deficiency,
+BMGC_DS14469,BMG_DS055037,,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1",,,,,DOID:0080468,developmental and epileptic encephalopathy 1,C3463992,,308350,MONDO:0010632,"developmental and epileptic encephalopathy, 1",
+BMGC_DS14470,BMG_DS055038,,"FANCONI ANEMIA, COMPLEMENTATION GROUP C",,,,,DOID:0111087,Fanconi anemia complementation group C,C3468041,,227645;613899,MONDO:0009213,Fanconi anemia complementation group C,
+BMGC_DS14471,BMG_DS055040,718555006,Juvenile amyotrophic lateral sclerosis,,,,,,,C3468114,,,MONDO:0017593,juvenile amyotrophic lateral sclerosis,Juvenile amyotrophic lateral sclerosis (disorder) | Juvenile amyotrophic lateral sclerosis | JALS - juvenile amyotrophic lateral sclerosis
+BMGC_DS14472,BMG_DS055044,,,,,,,,,C3468561,,,MONDO:0018054,familial atrial fibrillation,
+BMGC_DS14473,BMG_DS055059,,"HEMOCHROMATOSIS, TYPE 1",,,,,,,C3469186,,235200;613609,MONDO:0021001,hemochromatosis type 1,
+BMGC_DS14474,BMG_DS055061,,,,,,,,,C3469521,,227650,MONDO:0009215,Fanconi anemia complementation group A,
+BMGC_DS14475,BMG_DS055062,,"FANCONI ANEMIA, COMPLEMENTATION GROUP F",,,,,DOID:0111088,Fanconi anemia complementation group F,C3469526,,603467;613897,MONDO:0011325,Fanconi anemia complementation group F,
+BMGC_DS14476,BMG_DS055063,,,,,,,,,C3469527,,614082,MONDO:0013565,Fanconi anemia complementation group G,
+BMGC_DS14477,BMG_DS055064,,"FANCONI ANEMIA, COMPLEMENTATION GROUP L",,,,,DOID:0111082,Fanconi anemia complementation group L,C3469528,,608111;614083,MONDO:0013566,Fanconi anemia complementation group L,
+BMGC_DS14478,BMG_DS055065,,"FANCONI ANEMIA, COMPLEMENTATION GROUP P",,,,,DOID:0111092,Fanconi anemia complementation group P,C3469542,,613278;613951,MONDO:0013499,Fanconi anemia complementation group P,
+BMGC_DS14479,BMG_DS055066,,"PSEUDOHYPOALDOSTERONISM, TYPE IID",,,,,,,C3469605,,614495,MONDO:0013781,pseudohypoaldosteronism type 2D,
+BMGC_DS14480,BMG_DS055067,,"PSEUDOHYPOALDOSTERONISM, TYPE IIE",,,,,,,C3469606,,603136;614496,MONDO:0013782,pseudohypoaldosteronism type 2E,
+BMGC_DS14481,BMG_DS055071,450316000,Severe dehydration,,,,,,,C3472181,,MTHU047755,,,Severe dehydration (disorder) | Severe dehydration
+BMGC_DS14482,BMG_DS055080,,,,,,,,,C3472621,,,MONDO:0015690,myeloid neoplasm associated with PDGFRB rearrangement,
+BMGC_DS14483,BMG_DS055095,711158005,Spinocerebellar ataxia 36,,,,,,,C3472711,,614153,MONDO:0013594,spinocerebellar ataxia type 36,Spinocerebellar ataxia type 36 (disorder) | Spinocerebellar ataxia type 36 | Costa de Morte ataxia | Asidan ataxia | Spinocerebellar ataxia 36
+BMGC_DS14484,BMG_DS055096,,HERMANSKY-PUDLAK SYNDROME 4,,,,,DOID:0060542,Hermansky-Pudlak syndrome 4,C3484357,,606682;614073,MONDO:0013556,Hermansky-Pudlak syndrome 4,
+BMGC_DS14485,BMG_DS055097,,,,,,,DOID:12642,hiatus hernia,C3489393,,142400,MONDO:0007721,hiatus hernia,
+BMGC_DS14486,BMG_DS055098,,"Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial",Hyperlipoproteinemia Type V,,,,,,C3489395,D006954,,,,
+BMGC_DS14487,BMG_DS055099,,"Hypogonadism, Isolated Hypogonadotropic",Hypogonadism,,,,,,C3489396,D007006,,,,
+BMGC_DS14488,BMG_DS055102,,Hyperkalemic Periodic Paralysis Type 2,"Paralysis, Hyperkalemic Periodic",,,,,,C3489447,D020513,,,,
+BMGC_DS14489,BMG_DS055103,,,,,,,,,C3489529,,106600,MONDO:0007129,"tooth agenesis, selective, 1",
+BMGC_DS14490,BMG_DS055104,,Cone-Rod Dystrophy 2,Cone-Rod Dystrophies,,,,,,C3489532,D000071700,120970,MONDO:0007362,cone-rod dystrophy 2,
+BMGC_DS14491,BMG_DS055106,,"Stuttering, Familial Persistent 1",Stuttering,,,,DOID:0060243,stuttering,C3489627,D013342,184450,MONDO:0008483,"stuttering, familial persistent, 1",
+BMGC_DS14492,BMG_DS055107,,"Thrombocytosis, Autosomal Dominant","Thrombocythemia, Essential",,,,,,C3489628,D013920,,,,
+BMGC_DS14493,BMG_DS055108,,Vision Disability,Vision Disorders,,,,,,C3489704,D014786,,,,
+BMGC_DS14494,BMG_DS055109,,Aicardi-Goutieres Syndrome 2,,,,,,,C3489724,C535607,610181,MONDO:0012429,Aicardi-Goutieres syndrome 2,
+BMGC_DS14495,BMG_DS055110,,Pseudo-TORCH syndrome,,,,,,,C3489725,C535607,,MONDO:0009626,pseudo-TORCH syndrome,
+BMGC_DS14496,BMG_DS055111,,,,,,,DOID:0111724,geleophysic dysplasia,C3489726,,,MONDO:0000127,geleophysic dysplasia,
+BMGC_DS14497,BMG_DS055113,,Familial intrahepatic cholestasis of pregnancy,,,,,DOID:0070227,intrahepatic cholestasis of pregnancy,C3489728,C535932,,,,
+BMGC_DS14498,BMG_DS055114,236383002,Familial mesangial sclerosis,,,,,,,C3489732,C537346,,,,Familial mesangial sclerosis | Familial mesangial sclerosis (disorder)
+BMGC_DS14499,BMG_DS055115,193662007,Oculomotor apraxia,,,,,,,C3489733,,MTHU000629,,,Oculomotor apraxia | Oculomotor apraxia (disorder) | Oculomotor dyspraxia
+BMGC_DS14500,BMG_DS055116,,"Anti-plasmin deficiency, congenital",,,,,,,C3489734,C537777,,,,
+BMGC_DS14501,BMG_DS055118,,"Pituitary Hormone Deficiency, Combined, 3",,,,,,,C3489787,C536710,221750,MONDO:0009091,non-acquired combined pituitary hormone deficiency with spine abnormalities,
+BMGC_DS14502,BMG_DS055120,,,,,,,DOID:0070222,progressive familial intrahepatic cholestasis 2,C3489789,,601847,MONDO:0011156,progressive familial intrahepatic cholestasis type 2,
+BMGC_DS14503,BMG_DS055123,,,,,,,,,C3489793,,612965,MONDO:0013066,"46,XY sex reversal 3",
+BMGC_DS14504,BMG_DS055125,,"Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant",,,,,,,C3489795,C567925,,,,
+BMGC_DS14505,BMG_DS055126,,"Thyroid Hormone Resistance, Generalized, Autosomal Recessive",,,,,,,C3489796,C567936,274300,MONDO:0010131,"thyroid hormone resistance, generalized, autosomal recessive",
+BMGC_DS14506,BMG_DS055129,,Lentiginosis Profusa,,,,,,,C3492944,C573023,151001,MONDO:0007891,familial generalized lentiginosis,
+BMGC_DS14507,BMG_DS055130,,"HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1",,,,,,,C3493776,,275200;603372,MONDO:0010142,hypothyroidism due to TSH receptor mutations,
+BMGC_DS14508,BMG_DS055131,,Endemic Elephantiasis,Elephantiasis,,,,DOID:0050138,podoconiosis,C3494151,D004604,,,,
+BMGC_DS14509,BMG_DS055132,,Endemic Non-Filarial Elephantiasis,Elephantiasis,,,,DOID:0050138,podoconiosis,C3494152,D004604,,,,
+BMGC_DS14510,BMG_DS055133,,Bigfoot Disease,Elephantiasis,,,,DOID:0050138,podoconiosis,C3494153,D004604,,,,
+BMGC_DS14511,BMG_DS055134,,"Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous",Ovarian Hyperstimulation Syndrome,,,,,,C3494162,D016471,,,,
+BMGC_DS14512,BMG_DS055135,,,,,,,,,C3494175,,147251,MONDO:0007820,fused mandibular incisors,
+BMGC_DS14513,BMG_DS055136,,,,,,,,,C3494181,,168000,MONDO:0008192,paragangliomas 1,
+BMGC_DS14514,BMG_DS055137,,Autosomal Hemophilia A,Hemophilia A,,,,,,C3494186,D006467,,,,
+BMGC_DS14515,BMG_DS055138,,Factor VIII Deficiency,Hemophilia A,,,,,,C3494187,D006467,,,,
+BMGC_DS14516,BMG_DS055145,,"Autoimmune polyendocrinopathy syndrome, type 1",,,,,,,C3494489,C538275,,,,
+BMGC_DS14517,BMG_DS055146,,"Pseudohypoparathyroidism, Type Ia",Pseudohypoparathyroidism,,,,,,C3494506,D011547,103580,MONDO:0007078,pseudohypoparathyroidism type 1A,
+BMGC_DS14518,BMG_DS055147,,"Hypergonadotropic Ovarian Failure, X-Linked",Primary Ovarian Insufficiency,,,,,,C3494522,D016649,,,,
+BMGC_DS14519,BMG_DS055228,,,,,,,,,C3494934,,,MONDO:0019113,benign paroxysmal torticollis of infancy,
+BMGC_DS14520,BMG_DS055239,784345005,Malignant migrating partial seizures of infancy (disorder),,,,,,,C3494976,,,MONDO:0017385,malignant migrating partial seizures of infancy,MMPSI - malignant migrating partial seizures of infancy | Malignant migrating partial seizures of infancy (disorder) | Malignant migrating partial epilepsy of infancy | Malignant migrating partial seizures of infancy
+BMGC_DS14521,BMG_DS055261,,,,,,,,,C3495361,,137575,MONDO:0007660,familial ossifying fibroma,
+BMGC_DS14522,BMG_DS055264,,,,,,,,,C3495417,,164210,MONDO:0958175,craniofacial microsomia 1,
+BMGC_DS14523,BMG_DS055265,,Chromosome 18q syndrome,,,,,DOID:0060407,chromosome 18q deletion syndrome,C3495421,C536580,,,,
+BMGC_DS14524,BMG_DS055267,,Fanconi-Bickel Syndrome,Fanconi Syndrome,,,,DOID:0070562,Fanconi-Bickel syndrome,C3495427,D005198,227810,MONDO:0009216,glycogen storage disease due to GLUT2 deficiency,
+BMGC_DS14525,BMG_DS055269,,"Macular Degeneration, Age-Related, 2",,,,,,,C3495438,C562479,153800,MONDO:0007932,age related macular degeneration 2,
+BMGC_DS14526,BMG_DS055272,,Amish Brittle Hair Brain Syndrome,Trichothiodystrophy Syndromes,,,,DOID:0111868;DOID:2960,photosensitive trichothiodystrophy | nonphotosensitive trichothiodystrophy 5,C3495483,D054463,,,,
+BMGC_DS14527,BMG_DS055273,417604002,Axenfeld-Rieger syndrome,,,,Q13.81,,,C3495488,C535679,,MONDO:0019187,Axenfeld-Rieger syndrome,Axenfeld-Rieger syndrome (disorder) | Axenfeld-Rieger syndrome | Axenfeld syndrome
+BMGC_DS14528,BMG_DS055275,,Acrorenal Syndrome,,,,,DOID:0060347,acrorenal syndrome,C3495490,C563159,102520,MONDO:0007059,acrorenal syndrome,
+BMGC_DS14529,BMG_DS055276,,"Cardiomyopathy, Familial Hypertrophic, 1",,,,,,,C3495498,C566005,192600,MONDO:0008647,hypertrophic cardiomyopathy 1,
+BMGC_DS14530,BMG_DS055279,,,,,,,,,C3495537,,270100,MONDO:0700112,"heterotaxy, visceral, 5, autosomal",
+BMGC_DS14531,BMG_DS055282,,Dihydropyrimidinuria,Dihydropyrimidine Dehydrogenase Deficiency,,,,DOID:14218,dihydropyrimidine dehydrogenase deficiency,C3495551,D054067,,,,
+BMGC_DS14532,BMG_DS055284,61764000,Homocarnosinase deficiency,,,,,DOID:0060177,homocarnosinosis,C3495554,C535328,,,,Homocarnosinase deficiency | Homocarnosinosis | Homocarnosinase deficiency (disorder)
+BMGC_DS14533,BMG_DS055285,237924005;13271000;410052008,Carnosinemia,,,,,DOID:0060177,homocarnosinosis,C3495555,C535328,212200,MONDO:0008921,carnosinemia,Aminoacyl-histidine dipeptidase deficiency | Carnosinuria | Carnosinase deficiency | Carnosinaemia | Carnosinemia | Aminoacyl-histidine dipeptidase deficiency (disorder) | Aminoacyl-histidine dipeptidase deficiency | Aminoacyl-histidine dipeptidase deficiency (disorder) | Carnosinemia (disorder) | Carnosinaemia | Carnosinemia
+BMGC_DS14534,BMG_DS055287,239796000,Juvenile arthritis,,,,M08,,,C3495559,,MTHU070181;604302,MONDO:0011429,juvenile idiopathic arthritis,Juvenile chronic arthritis | Juvenile arthritis | JCA - Juvenile chronic arthritis | Juvenile chronic arthritis (disorder)
+BMGC_DS14535,BMG_DS055289,,"Night Blindness, Congenital Stationary, Type 1A",,,,,,,C3495587,C536122,310500,MONDO:0010690,congenital stationary night blindness 1A,
+BMGC_DS14536,BMG_DS055290,,Acrocephalopolydactylous Dysplasia,,,,,,,C3495588,C573722,200995,MONDO:0008709,acrocephalopolydactyly,
+BMGC_DS14537,BMG_DS055291,707608003,Jalili syndrome,,,,,DOID:0111404,Jalili syndrome,C3495589,C000596385,217080,MONDO:0009007,Jalili syndrome,Jalili syndrome | Amelogenesis imperfecta co-occurrent with cone rod dystrophy | Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder)
+BMGC_DS14538,BMG_DS055293,,"Charcot-Marie-Tooth Disease, Demyelinating, Type 1e",,,,,,,C3495591,C566136,118300,MONDO:0007311,Charcot-Marie-Tooth disease type 1E,
+BMGC_DS14539,BMG_DS055295,,,,,,,,,C3495676,,107100,MONDO:0007136,hereditary anorectal anomalies,
+BMGC_DS14540,BMG_DS055296,,NF1 Microduplication Syndrome,,,,,,,C3495679,C567173,618874,MONDO:0015350,17q11.2 microduplication syndrome,
+BMGC_DS14541,BMG_DS055298,195353004,Granulomatosis with polyangiitis,,4A44.A1,Granulomatosis with polyangiitis,M31.3,DOID:12132,granulomatosis with polyangiitis,C3495801,,608710,MONDO:0012105,granulomatosis with polyangiitis,Necrotising respiratory granulomatosis | Necrotizing respiratory granulomatosis | Granulomatosis with polyangiitis | Granulomatosis with polyangiitis (disorder)
+BMGC_DS14542,BMG_DS055300,,Nonepileptic Seizures,Seizures,,,,,,C3495874,D012640,,,,
+BMGC_DS14543,BMG_DS055304,,"Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia",,,,,,,C3496228,C567311,612319,MONDO:0012866,hereditary spastic paraplegia 35,
+BMGC_DS14544,BMG_DS055306,,,,,,,,,C3496337,,,MONDO:0018170,idiopathic nephrotic syndrome,
+BMGC_DS14545,BMG_DS055307,471268000,Middle aortic syndrome,,,,,,,C3496579,,,MONDO:0015446,atypical coarctation of aorta,Middle aortic syndrome | Middle aortic syndrome (disorder)
+BMGC_DS14546,BMG_DS055308,,Parkinson Disease 13,,,,,,,C3496588,C565204,,,,
+BMGC_DS14547,BMG_DS055311,,"Nephrotic Syndrome, Congenital, With Ocular Abnormalities And Congenital Myasthenic Syndrome",,,,,,,C3501249,C537185,,,,
+BMGC_DS14548,BMG_DS055312,,"Deafness, Sensorineural, with Hypertrophic Cardiomyopathy",,,,,,,C3501265,C565236,,,,
+BMGC_DS14549,BMG_DS055314,,"Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosomal Recessive",,,,,,,C3501372,C567624,,,,
+BMGC_DS14550,BMG_DS055316,,Mental Retardation associated with Psoriasis,,,,,,,C3501539,C564107,309480,MONDO:0010652,X-linked intellectual disability-seizures-psoriasis syndrome,
+BMGC_DS14551,BMG_DS055319,,"Mental Retardation, X-Linked Nonsyndromic",,,,,,,C3501611,C564490,,MONDO:0019181,non-syndromic X-linked intellectual disability,
+BMGC_DS14552,BMG_DS055320,,"Generalized Epilepsy With Febrile Seizures Plus, Type 5",,,,,,,C3501643,C565812,,,,
+BMGC_DS14553,BMG_DS055321,,"Glutathione Peroxidase Deficiency, Hemolytic Anemia possibly due to",,,,,,,C3501647,C564217,,,,
+BMGC_DS14554,BMG_DS055324,,Bleeding Disorder due to Defective Thromboxane A2 Receptor,,,,,,,C3501679,C566055,,,,
+BMGC_DS14555,BMG_DS055326,,T-Cell OKT4 Deficiency,,,,,,,C3501681,C566080,,,,
+BMGC_DS14556,BMG_DS055337,,"Microcephaly, Primary Autosomal Recessive, 2",,,,,,,C3501830,C565794,,,,
+BMGC_DS14557,BMG_DS055345,,"Night blindness, congenital stationary, type 1",,,,,,,C3501847,C536122,,,,
+BMGC_DS14558,BMG_DS055346,,"Nephrosis, congenital",,,,,DOID:2590,familial nephrotic syndrome,C3501848,C535761,,MONDO:0002350,familial nephrotic syndrome,
+BMGC_DS14559,BMG_DS055347,,Mngie Without Leukoencephalopathy,,,,,DOID:0080127;DOID:0070331;DOID:0080119,mitochondrial DNA depletion syndrome 8b | mitochondrial DNA depletion syndrome 8a | mitochondrial DNA depletion syndrome 1,C3501849,C536350,,,,
+BMGC_DS14560,BMG_DS055352,,,,,,,,,C3501854,,308960,MONDO:0700060,"leukemia, acute, X-linked",
+BMGC_DS14561,BMG_DS055355,,"Muscular Dystrophy, Limb-Girdle, Type 1D",,,,,,,C3501858,C566370,,,,
+BMGC_DS14562,BMG_DS055357,,"Mitochondrial DNA Depletion Syndrome, Myopathic Form",,,,,DOID:0080120,mitochondrial DNA depletion syndrome 2,C3501891,C563698,,,,
+BMGC_DS14563,BMG_DS055362,,Cerebrocostomandibular-Like Syndrome,,,,,,,C3501912,C562538,,,,
+BMGC_DS14564,BMG_DS055371,,"Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive",,,,,,,C3502051,C567348,,,,
+BMGC_DS14565,BMG_DS055372,,"Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant",,,,,,,C3502052,C567347,,,,
+BMGC_DS14566,BMG_DS055373,,"Leukodystrophy, Dysmyelinating, with Oligodontia",,,,,,,C3502054,C564344,,MONDO:0019177,odontoleukodystrophy,
+BMGC_DS14567,BMG_DS055378,,"Woolly Hair, Autosomal Recessive",,,,,,,C3502073,C564735,,,,
+BMGC_DS14568,BMG_DS055379,,Multiple Mitochondrial Dysfunctions Syndrome,,,,,DOID:0070330,multiple mitochondrial dysfunctions syndrome,C3502075,C565304,,MONDO:0017338,fatal multiple mitochondrial dysfunctions syndrome,
+BMGC_DS14569,BMG_DS055380,,"Dyskeratosis Congenita, Autosomal Recessive",,,,,,,C3502105,C565611,,,,
+BMGC_DS14570,BMG_DS055385,,"Homocystinuria, Pyridoxine-Responsive",,,,,,,C3502110,C565513,,,,
+BMGC_DS14571,BMG_DS055386,,"Adrenal Insufficiency, Congenital",,,,,,,C3502131,C566130,,,,
+BMGC_DS14572,BMG_DS055387,,"Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal",,,,,,,C3502132,C566131,,,,
+BMGC_DS14573,BMG_DS055394,,Microcephalic Osteodysplastic Primordial Dwarfism with Tooth Abnormalities,,,,,DOID:0060609,microcephalic osteodysplastic primordial dwarfism type II,C3502214,C565898,,,,
+BMGC_DS14574,BMG_DS055400,,"Deafness, Autosomal Recessive 36, Without Vestibular Involvement",,,,,,,C3502293,C567219,,,,
+BMGC_DS14575,BMG_DS055406,,Atresia of External Auditory Canal and Conduction Deafness,,,,,,,C3502361,C566245,108760,MONDO:0007170,atresia of external auditory canal and conductive deafness,
+BMGC_DS14576,BMG_DS055419,,"Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia",,,,,,,C3502469,C564519,,MONDO:0019414,BRESEK syndrome,
+BMGC_DS14577,BMG_DS055420,,"Microcephaly with Chorioretinopathy, Autosomal Recessive",,,,,,,C3502492,C565379,,,,
+BMGC_DS14578,BMG_DS055421,,Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal,,,,,,,C3502495,C565693,,,,
+BMGC_DS14579,BMG_DS055432,,Generalized Epilepsy with Febrile Seizures Plus,,,,,DOID:0060170,generalized epilepsy with febrile seizures plus,C3502809,C565808,,MONDO:0018214,generalized epilepsy with febrile seizures plus,
+BMGC_DS14580,BMG_DS055463,,,,,,,,,C3508773,,,MONDO:0020521,Ehlers-Danlos syndrome type 7A,
+BMGC_DS14581,BMG_DS055638,472315005,Mitochondrial cardiomyopathy,,,,,,,C3532239,,,,,Mitochondrial cardiomyopathy (disorder) | Mitochondrial cardiomyopathy
+BMGC_DS14582,BMG_DS055642,472319004,Fatal infantile mitochondrial cardiomyopathy,,,,,,,C3532243,,,,,Fatal infantile mitochondrial cardiomyopathy (disorder) | Fatal infantile mitochondrial cardiomyopathy
+BMGC_DS14583,BMG_DS055645,472323007,Fetal cardiomyopathy,,,,,,,C3532247,,,,,Fetal cardiomyopathy | Fetal cardiomyopathy (disorder) | Foetal cardiomyopathy
+BMGC_DS14584,BMG_DS055736,,,,,,,,,C3536714,,,MONDO:0019638,renal dysplasia,
+BMGC_DS14585,BMG_DS055737,84137001;274945004,AA amyloidosis,,,,,,,C3536715,C000718787,,MONDO:0019439,AA amyloidosis,AA amyloidosis | AA amyloidosis (disorder) | AA amyloidosis | Amyloid A amyloidosis (disorder) | Amyloid A amyloidosis
+BMGC_DS14586,BMG_DS055738,858580008,Secondary systemic amyloidosis,,5D00.1,AA amyloidosis,E85.3,DOID:0080936,serum amyloid A amyloidosis,C3536716,,,,,Secondary systemic amyloidosis (disorder) | Secondary systemic amyloidosis
+BMGC_DS14587,BMG_DS055741,,Ichthyosis Congenita II,"Ichthyosis, Lamellar",,,,,,C3536797,D017490,,,,
+BMGC_DS14588,BMG_DS055746,,Familial Hypophosphatemic Rickets,Familial Hypophosphatemic Rickets,,,,,,C3536983,D053098,,MONDO:0019642,"vitamin D-dependent rickets, type 2",
+BMGC_DS14589,BMG_DS055747,,"Vitamin D-Resistant Rickets, X-Linked",Familial Hypophosphatemic Rickets,,,,,,C3536984,D053098,,,,
+BMGC_DS14590,BMG_DS055748,,,,,,,DOID:5852,inferolateral myocardial infarct,C3537017,,,MONDO:0003676,inferolateral myocardial infarct,
+BMGC_DS14591,BMG_DS055749,,Ménière's Vertigo,Meniere Disease,,,,,,C3537146,D008575,,,,
+BMGC_DS14592,BMG_DS055752,,"Cystinosis, Infantile Nephropathic",,,,,,,C3537440,C565655,,MONDO:0018467,nephropathic infantile cystinosis,
+BMGC_DS14593,BMG_DS055753,,,,,,,,,C3538945,,148000,MONDO:0007845,"Kaposi sarcoma, susceptibility to",
+BMGC_DS14594,BMG_DS055754,,"DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT",,,,,,,C3538946,,600791;601093;605646,MONDO:0010933,autosomal recessive nonsyndromic hearing loss 4,
+BMGC_DS14595,BMG_DS055755,,"MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA",,,,,,,C3538951,,602091;251750,MONDO:0009633,"microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma",
+BMGC_DS14596,BMG_DS055756,,DYSTONIA 23,,,,,,,C3538999,,614860,MONDO:0013928,dystonia 23,
+BMGC_DS14597,BMG_DS055757,1279838005,Hereditary sensory and autonomic neuropathy type 6,,,,,,,C3539003,,614653,MONDO:0013839,hereditary sensory and autonomic neuropathy type 6,Hereditary sensory and autonomic neuropathy type 6 (disorder) | Familial dysautonomia with contractures | Hereditary sensory and autonomic neuropathy type VI | Hereditary sensory and autonomic neuropathy type 6 | HSAN6 - hereditary sensory and autonomic neuropathy type 6
+BMGC_DS14598,BMG_DS055758,,"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP F",,,,,DOID:0080480,peroxisome biogenesis disorder 5A,C3539010,,614866,,,
+BMGC_DS14599,BMG_DS055759,,AICARDI-GOUTIERES SYNDROME 6,,,,,,,C3539013,,146920;615010,MONDO:0014007,Aicardi-Goutieres syndrome 6,
+BMGC_DS14600,BMG_DS055760,,NEPHRONOPHTHISIS 14,,,,,DOID:0111122,nephronophthisis 14,C3539071,,604557;614844,MONDO:0013916,nephronophthisis 14,
+BMGC_DS14601,BMG_DS055761,,,,,,,,,C3539120,,614731,MONDO:0013872,"prostate cancer, hereditary, 2",
+BMGC_DS14602,BMG_DS055762,,"CEROID LIPOFUSCINOSIS, NEURONAL, 11",,,,,,,C3539123,,138945;614706,MONDO:0013866,neuronal ceroid lipofuscinosis 11,
+BMGC_DS14603,BMG_DS055763,,"USHER SYNDROME, TYPE IK",,,,,,,C3539124,,614990,MONDO:0014001,Usher syndrome type 1K,
+BMGC_DS14604,BMG_DS055764,,"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A",,,,,DOID:0080482,peroxisome biogenesis disorder 7A,C3539168,,614872,,,
+BMGC_DS14605,BMG_DS055765,,"TREMOR, HEREDITARY ESSENTIAL, 4",,,,,DOID:0111431,essential tremor 4,C3539195,,614782;137070,MONDO:0013888,"tremor, hereditary essential, 4",
+BMGC_DS14606,BMG_DS055766,,"SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE",,,,,,,C3539494,,614898;609927,MONDO:0013962,hereditary spastic paraplegia 53,
+BMGC_DS14607,BMG_DS055767,,"SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE",,,,,,,C3539495,,615003;615033,MONDO:0014018,hereditary spastic paraplegia 54,
+BMGC_DS14608,BMG_DS055768,,"SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE",,,,,,,C3539506,,615035;613541,MONDO:0014020,hereditary spastic paraplegia 55,
+BMGC_DS14609,BMG_DS055769,,"SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE",,,,,,,C3539507,,610670;615030,MONDO:0014015,hereditary spastic paraplegia 56,
+BMGC_DS14610,BMG_DS055770,,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3",,,,,,,C3539888,,606545;607206,MONDO:0011680,autosomal recessive congenital ichthyosis 3,
+BMGC_DS14611,BMG_DS055771,,"MYOCLONUS, FAMILIAL CORTICAL",,,,,,,C3539916,,614937,MONDO:0100093,"myoclonus, familial, 1",
+BMGC_DS14612,BMG_DS055772,,"ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE",,,,,DOID:0111654,ectodermal dysplasia 11B,C3539920,,614941;606603,MONDO:0013983,"ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive",
+BMGC_DS14613,BMG_DS055773,,HYPOGONADOTROPIC HYPOGONADISM 14 WITH OR WITHOUT ANOSMIA,,,,,,,C3540450,,614858,MONDO:0013926,hypogonadotropic hypogonadism 14 with or without anosmia,
+BMGC_DS14614,BMG_DS055774,,"CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F",,,,,,,C3540453,,614895,MONDO:0013959,Charcot-Marie-Tooth disease type 4F,
+BMGC_DS14615,BMG_DS055775,,Congenital Amaurosis of Retinal Origin,Leber Congenital Amaurosis,,,,,,C3540662,D057130,,,,
+BMGC_DS14616,BMG_DS055776,,"CILIARY DYSKINESIA, PRIMARY, 20",,,,,,,C3540844,,615038;615067,MONDO:0014030,primary ciliary dyskinesia 20,
+BMGC_DS14617,BMG_DS055777,,"MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 8",,,,,,,C3540845,,610745,MONDO:0800324,"microphthalmia, isolated, with coloboma 8",
+BMGC_DS14618,BMG_DS055778,,"CATARACT 4, MULTIPLE TYPES",,,,,,,C3540850,,115700;123690,MONDO:0007281,cataract 4 multiple types,
+BMGC_DS14619,BMG_DS055779,,"Rickets, X-Linked Hypophosphatemic",Familial Hypophosphatemic Rickets,,,,DOID:0050445,X-linked dominant hypophosphatemic rickets,C3540852,D053098,,MONDO:0020720,X-linked hypophosphatemic rickets,
+BMGC_DS14620,BMG_DS055780,,"SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY",,,,,,,C3541319,,608025;614800,MONDO:0013889,short stature-optic atrophy-Pelger-HuC+t anomaly syndrome,
+BMGC_DS14621,BMG_DS055781,,PONTINE TEGMENTAL CAP DYSPLASIA,,,,,,,C3541340,,614688,MONDO:0013858,pontine tegmental cap dysplasia,
+BMGC_DS14622,BMG_DS055783,,,,,,,,,C3541456,,313400,MONDO:0010737,"spondyloepiphyseal dysplasia tarda, X-linked",
+BMGC_DS14623,BMG_DS055786,,HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA,,,,,,,C3541462,,614842,MONDO:0013915,hypogonadotropic hypogonadism 13 with or without anosmia,
+BMGC_DS14624,BMG_DS055787,,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1",,,,,DOID:0080111,mitochondrial complex III deficiency nuclear type 1,C3541471,,603647;124000,MONDO:0007415,mitochondrial complex III deficiency nuclear type 1,
+BMGC_DS14625,BMG_DS055788,,"ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE",,,,,DOID:0111149,autosomal recessive isolated ectopia lentis 2,C3541474,,610113;225100,MONDO:0009152,"ectopia lentis 2, isolated, autosomal recessive",
+BMGC_DS14626,BMG_DS055789,,"MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET, MILD VARIANT",,,,,DOID:0081345,congenital myopathy 10B,C3541476,,620249,MONDO:0859515,"congenital myopathy 10b, mild variant",
+BMGC_DS14627,BMG_DS055790,,"ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT",,,,,DOID:0111653,ectodermal dysplasia 11A,C3541517,,606603;614940,MONDO:0013982,"ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant",
+BMGC_DS14628,BMG_DS055791,,"ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT",,,,,,,C3541518,,129600;134797,MONDO:0007514,"ectopia lentis 1, isolated, autosomal dominant",
+BMGC_DS14629,BMG_DS055792,,NEPHRONOPHTHISIS 15,,,,,DOID:0111123,nephronophthisis 15,C3541853,,614845;614848,MONDO:0013917,nephronophthisis 15,
+BMGC_DS14630,BMG_DS055793,,Drug Hypersensitivity Syndrome,Drug Hypersensitivity Syndrome,,,,,,C3541994,D063926,,MONDO:0015340,drug rash with eosinophilia and systemic symptoms,
+BMGC_DS14631,BMG_DS055794,,Duchenne and Becker Muscular Dystrophy,"Muscular Dystrophy, Duchenne",,,,,,C3542021,D020388,,,,
+BMGC_DS14632,BMG_DS055795,773625007,"Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome",,,,,,,C3542022,,614813,MONDO:0013894,short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome,"SOFT syndrome | Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) | Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome | SOFT (short stature, onychodysplasia, facial dysmorphism, hypotrichosis) syndrome"
+BMGC_DS14633,BMG_DS055796,,AORTIC VALVE DISEASE 2,,,,,DOID:0080334,aortic valve disease 2,C3542024,,602931;614823,MONDO:0013902,aortic valve disease 2,
+BMGC_DS14634,BMG_DS055797,,"AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE",,,,,,,C3542025,,105400;147450,,,
+BMGC_DS14635,BMG_DS055798,,PEROXISOME BIOGENESIS DISORDER 5B,,,,,DOID:0081434,Peroxisome biogenesis disorder 5B,C3542026,,614867;170993,MONDO:0013933,peroxisome biogenesis disorder 5B,
+BMGC_DS14636,BMG_DS055799,,Aminoacylase 2 Deficiency,Canavan Disease,,,,,,C3542499,D017825,,,,
+BMGC_DS14637,BMG_DS055800,,ADH-Resistant Diabetes Insipidus,"Diabetes Insipidus, Nephrogenic",,,,,,C3542500,D018500,,,,
+BMGC_DS14638,BMG_DS055801,,"NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IX, WITH DEVELOPMENTAL DELAY",,,,,,,C3542549,,615031;615000,MONDO:0014016,hereditary spastic paraplegia 49,
+BMGC_DS14639,BMG_DS055802,,"CILIARY DYSKINESIA, PRIMARY, 17",,,,,,,C3542550,,614677;614679,MONDO:0013854,primary ciliary dyskinesia 17,
+BMGC_DS14640,BMG_DS055803,,"IMMUNODEFICIENCY, COMMON VARIABLE, 7",,,,,DOID:0081150,common variable immunodeficiency 7,C3542922,,120650;614699,MONDO:0013862,"immunodeficiency, common variable, 7",
+BMGC_DS14641,BMG_DS055805,,"CILIARY DYSKINESIA, PRIMARY, 18",,,,,,,C3543825,,614864;614874,MONDO:0013940,primary ciliary dyskinesia 18,
+BMGC_DS14642,BMG_DS055806,,"CILIARY DYSKINESIA, PRIMARY, 19",,,,,,,C3543826,,614930;614935,MONDO:0013979,primary ciliary dyskinesia 19,
+BMGC_DS14643,BMG_DS055809,,Collodion Fetus,"Ichthyosis, Lamellar",,,,,,C3543867,D017490,,,,
+BMGC_DS14644,BMG_DS055815,,,,,,,,,C3544321,,,MONDO:0005414,treatment-refractory schizophrenia,
+BMGC_DS14645,BMG_DS055818,,ALTERNATING HEMIPLEGIA OF CHILDHOOD 1,,,,,,,C3549447,,104290;182340,MONDO:0007087,alternating hemiplegia of childhood 1,
+BMGC_DS14646,BMG_DS055819,,NOR POLYAGGLUTINATION SYNDROME,,,,,,,C3549486,,111400;607922,,,
+BMGC_DS14647,BMG_DS055820,,ACAMPOMELIC CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL,,,,,,,C3549544,,608160;114290,,,
+BMGC_DS14648,BMG_DS055826,,"CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1",,,,,DOID:0070228,intrahepatic cholestasis of pregnancy 1,C3549845,,602397;147480,MONDO:0007829,"cholestasis, intrahepatic, of pregnancy, 1",
+BMGC_DS14649,BMG_DS055827,,"MACROGLOBULINEMIA, WALDENSTROM, SOMATIC",,,,,,,C3549870,,602170,,,
+BMGC_DS14650,BMG_DS055829,,METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA WITH OR WITHOUT BRACHYDACTYLY,,,,,DOID:0111513,metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome,C3549874,,156510,MONDO:0007984,metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome,
+BMGC_DS14651,BMG_DS055831,,,,,,,,,C3550234,,202370,MONDO:0008736,peroxisome biogenesis disorder 2B,
+BMGC_DS14652,BMG_DS055832,,,,,,,,,C3550273,,214110,MONDO:0008954,peroxisome biogenesis disorder 2A (Zellweger),
+BMGC_DS14653,BMG_DS055833,,"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 2",,,,,DOID:0080477,peroxisome biogenesis disorder 2A,C3550274,,214110,MONDO:0800298,"peroxisome biogenesis disorder, complementation group 2",
+BMGC_DS14654,BMG_DS055836,,"HYPERBILIRUBINEMIA, SHUNT, PRIMARY",,,,,,,C3550398,,237800,MONDO:0009382,"hyperbilirubinemia, shunt, primary",
+BMGC_DS14655,BMG_DS055841,,HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA,,,,,,,C3550478,,244200;607123,MONDO:0009482,hypogonadotropic hypogonadism 3 with or without anosmia,
+BMGC_DS14656,BMG_DS055843,,"POLYDACTYLY, POSTAXIAL, TYPE A5",,,,,,,C3550661,,263450,MONDO:0009893,"polydactyly, postaxial, type A5",
+BMGC_DS14657,BMG_DS055844,,PEROXISOME BIOGENESIS DISORDER 3B,,,,,DOID:0081241,peroxisome biogenesis disorder 3B,C3550693,,266510,MONDO:0009959,peroxisome biogenesis disorder type 3B,
+BMGC_DS14658,BMG_DS055846,,"THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA",,,,,,,C3550789,,300367,MONDO:0010308,"thrombocytopenia, X-linked, with or without dyserythropoietic anemia",
+BMGC_DS14659,BMG_DS055847,,"ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES",,,,,DOID:0112156,X-linked dyserythropoietic anemia,C3550856,,305371;300835,MONDO:0010444,X-linked dyserythropoetic anemia with abnormal platelets and neutropenia,
+BMGC_DS14660,BMG_DS055849,,"AUTISM, SUSCEPTIBILITY TO, X-LINKED 6",,,,,,,C3550875,,300777;300872,MONDO:0010469,epsilon-trimethyllysine hydroxylase deficiency,
+BMGC_DS14661,BMG_DS055850,,CORNELIA DE LANGE SYNDROME 5,,,,,DOID:0080509,Cornelia de Lange syndrome 5,C3550903,,300269;300882,MONDO:0010471,Cornelia de Lange syndrome 5,
+BMGC_DS14662,BMG_DS055851,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 32",,,,,DOID:0060828,X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome,C3550913,,300886,MONDO:0010473,X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome,
+BMGC_DS14663,BMG_DS055852,,LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2,,,,,DOID:0111877,linear skin defects with multiple congenital anomalies 2,C3550921,,300885;300887,MONDO:0010474,linear skin defects with multiple congenital anomalies 2,
+BMGC_DS14664,BMG_DS055854,,"HYPOTHYROIDISM, CENTRAL, WITH TESTICULAR ENLARGEMENT",,,,,,,C3550963,,300137;300888,MONDO:0010475,X-linked central congenital hypothyroidism with late-onset testicular enlargement,
+BMGC_DS14665,BMG_DS055855,,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5,,,,,,,C3550973,,300526;300894,MONDO:0010476,neurodegeneration with brain iron accumulation 5,
+BMGC_DS14666,BMG_DS055856,,CHROMOSOME Xq21 DELETION SYNDROME,,,,,,,C3551019,,303110,MONDO:0010558,choroideremia-deafness-obesity syndrome,
+BMGC_DS14667,BMG_DS055860,,"PAROTID SALIVARY GLANDS, POLYCYSTIC DYSGENETIC DISEASE OF",,,,,,,C3551133,,600343,MONDO:0010872,"parotid salivary glands, polycystic dysgenetic disease of",
+BMGC_DS14668,BMG_DS055861,,UV-SENSITIVE SYNDROME 1,,,,,,,C3551173,,609413;600630,MONDO:0010909,UV-sensitive syndrome 1,
+BMGC_DS14669,BMG_DS055863,,"ECTODERMAL DYSPLASIA 8, HAIR/TOOTH/NAIL TYPE",,,,,,,C3551424,,602401,MONDO:0011219,Fried's tooth and nail syndrome,
+BMGC_DS14670,BMG_DS055864,,ANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT,,,,,,,C3551443,,602588,,,
+BMGC_DS14671,BMG_DS055866,,CORTISONE REDUCTASE DEFICIENCY 1,,,,,DOID:0090141,cortisone reductase deficiency 1,C3551716,,604931;138090,MONDO:0011503,cortisone reductase deficiency 1,
+BMGC_DS14672,BMG_DS055868,,,,,,,,,C3551915,,607174,MONDO:0011789,familial meningioma,
+BMGC_DS14673,BMG_DS055869,,"COENZYME Q10 DEFICIENCY, PRIMARY, 1",,,,,DOID:0070238,primary coenzyme Q10 deficiency 1,C3551954,,607426;609825,MONDO:0011829,"coenzyme Q10 deficiency, primary, 1",
+BMGC_DS14674,BMG_DS055870,,ACHROMATOPSIA 6,,,,,,,C3552227,,601190;610024,MONDO:0800197,achromatopsia 6,
+BMGC_DS14675,BMG_DS055871,,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7",,,,,DOID:0090132,complex cortical dysplasia with other brain malformations 7,C3552236,,610031;612850,MONDO:0012399,complex cortical dysplasia with other brain malformations 7,
+BMGC_DS14676,BMG_DS055873,,"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH MILD PALMOPLANTAR KERATODERMA AND WOOLLY HAIR",,,,,,,C3552311,,125645,,,
+BMGC_DS14677,BMG_DS055874,,"MYASTHENIC SYNDROME, CONGENITAL, 12",,,,,DOID:0110660,congenital myasthenic syndrome 12,C3552335,,138292;610542,MONDO:0012518,congenital myasthenic syndrome 12,
+BMGC_DS14678,BMG_DS055875,,HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA,,,,,,,C3552343,,607002;610628,MONDO:0012528,hypogonadotropic hypogonadism 4 with or without anosmia,
+BMGC_DS14679,BMG_DS055883,,HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA,,,,,,,C3552553,,612370,MONDO:0012880,hypogonadotropic hypogonadism 5 with or without anosmia,
+BMGC_DS14680,BMG_DS055884,,HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA,,,,,,,C3552574,,600483;612702,MONDO:0012988,hypogonadotropic hypogonadism 6 with or without anosmia,
+BMGC_DS14681,BMG_DS055885,,LYMPHOPROLIFERATIVE SYNDROME 1,,,,,,,C3552634,,186973;613011,MONDO:0013081,lymphoproliferative syndrome 1,
+BMGC_DS14682,BMG_DS055886,,RETINITIS PIGMENTOSA 65,,,,,DOID:0111021,cone-rod dystrophy 15,C3552852,,613660;609502,MONDO:0800352,retinitis pigmentosa 65,
+BMGC_DS14683,BMG_DS055888,,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8",,,,,,,C3553029,,613943;613924,MONDO:0013495,autosomal recessive congenital ichthyosis 8,
+BMGC_DS14684,BMG_DS055889,,"EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT",,,,,DOID:0070252,autosomal dominant Emery-Dreifuss muscular dystrophy 7,C3553060,,612048;614302,MONDO:0013677,"Emery-Dreifuss muscular dystrophy 7, autosomal dominant",
+BMGC_DS14685,BMG_DS055890,,"MICROPHTHALMIA, SYNDROMIC 11",,,,,DOID:0111804,syndromic microphthalmia 11,C3553077,,614402;604294,MONDO:0013734,"microphthalmia, syndromic 11",
+BMGC_DS14686,BMG_DS055893,1220574003,COG6-CGD - component of oligomeric golgi complex 6-congenital disorder of glycosylation,,,,,,,C3553230,,614576,MONDO:0013810,COG6-congenital disorder of glycosylation,Component of oligomeric golgi complex 6-congenital disorder of glycosylation | Component of oligomeric golgi complex 6-congenital disorder of glycosylation (disorder) | Congenital disorder of glycosylation type 2l | COG6-CGD - component of oligomeric golgi complex 6-congenital disorder of glycosylation | Congenital disorder of glycosylation type IIL
+BMGC_DS14687,BMG_DS055894,,COFFIN-SIRIS SYNDROME 2,,,,,DOID:0070044,Coffin-Siris syndrome 2,C3553247,,603024;614607,MONDO:0013819,"intellectual disability, autosomal dominant 14",
+BMGC_DS14688,BMG_DS055895,,COFFIN-SIRIS SYNDROME 3,,,,,DOID:0070045,Coffin-Siris syndrome 3,C3553248,,614608;601607,MONDO:0013820,"intellectual disability, autosomal dominant 15",
+BMGC_DS14689,BMG_DS055896,,COFFIN-SIRIS SYNDROME 4,,,,,DOID:0070046,Coffin-Siris syndrome 4,C3553249,,614609;603254,MONDO:0013821,"intellectual disability, autosomal dominant 16",
+BMGC_DS14690,BMG_DS055897,,ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE,,,,,,,C3553250,,614613,MONDO:0013822,acrodysostosis 2 with or without hormone resistance,
+BMGC_DS14691,BMG_DS055898,,JOUBERT SYNDROME 17,,,,,DOID:0110986,Joubert syndrome 17,C3553264,,614615;614571,MONDO:0013824,Joubert syndrome 17,
+BMGC_DS14692,BMG_DS055899,,DIARRHEA 6,,,,,,,C3553270,,601330;614616,MONDO:0013825,congenital diarrhea 6,
+BMGC_DS14693,BMG_DS055907,,HYPEREKPLEXIA 3,,,,,,,C3553288,,614618,MONDO:0013827,hyperekplexia 3,
+BMGC_DS14694,BMG_DS055908,,HYPEREKPLEXIA 2,,,,,,,C3553291,,138492;614619,MONDO:0013828,hyperekplexia 2,
+BMGC_DS14695,BMG_DS055909,,UV-SENSITIVE SYNDROME 2,,,,,,,C3553298,,609412;614621,MONDO:0013829,UV-sensitive syndrome 2,
+BMGC_DS14696,BMG_DS055910,,KERATOCONUS 5,,,,,,,C3553302,,614622,MONDO:0013830,keratoconus 5,
+BMGC_DS14697,BMG_DS055911,,KERATOCONUS 6,,,,,,,C3553306,,614623,MONDO:0013831,keratoconus 6,
+BMGC_DS14698,BMG_DS055912,,KERATOCONUS 8,,,,,,,C3553307,,614628,MONDO:0013832,keratoconus 8,
+BMGC_DS14699,BMG_DS055913,,KERATOCONUS 7,,,,,,,C3553308,,614629,MONDO:0013833,keratoconus 7,
+BMGC_DS14700,BMG_DS055914,,UV-SENSITIVE SYNDROME 3,,,,,,,C3553328,,614632;614640,MONDO:0013834,UV-sensitive syndrome 3,
+BMGC_DS14701,BMG_DS055915,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7",,,,,DOID:0111234,congenital muscular dystrophy-dystroglycanopathy A7,C3553330,,614631;614643,MONDO:0013835,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7",
+BMGC_DS14702,BMG_DS055916,,"COENZYME Q10 DEFICIENCY, PRIMARY, 6",,,,,DOID:0070243,primary coenzyme Q10 deficiency 6,C3553349,,614647;614650,MONDO:0013836,familial steroid-resistant nephrotic syndrome with sensorineural deafness,
+BMGC_DS14703,BMG_DS055917,,"COENZYME Q10 DEFICIENCY, PRIMARY, 2",,,,,DOID:0070239,primary coenzyme Q10 deficiency 2,C3553354,,607429;614651,MONDO:0013837,deafness-encephaloneuropathy-obesity-valvulopathy syndrome,
+BMGC_DS14704,BMG_DS055918,,"COENZYME Q10 DEFICIENCY, PRIMARY, 3",,,,,DOID:0070240,primary coenzyme Q10 deficiency 3,C3553358,,614652;610564,MONDO:0013838,"coenzyme Q10 deficiency, primary, 3",
+BMGC_DS14705,BMG_DS055919,,"COENZYME Q10 DEFICIENCY, PRIMARY, 5",,,,,DOID:0070242,primary coenzyme Q10 deficiency 5,C3553374,,612837;614654,MONDO:0013840,encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome,
+BMGC_DS14706,BMG_DS055921,,CORTISONE REDUCTASE DEFICIENCY 2,,,,,DOID:0090140,cortisone reductase deficiency 2,C3553382,,600713;614662,MONDO:0013842,cortisone reductase deficiency 2,
+BMGC_DS14707,BMG_DS055923,,"STUTTERING, FAMILIAL PERSISTENT, 4",,,,,,,C3553403,,614668,MONDO:0013844,"stuttering, familial persistent, 4",
+BMGC_DS14708,BMG_DS055924,,AURICULOCONDYLAR SYNDROME 2A,,,,,,,C3553404,,600810;614669,MONDO:0013845,auriculocondylar syndrome 2,
+BMGC_DS14709,BMG_DS055926,,CHROMOSOME 16p11.2 DUPLICATION SYNDROME,,,,,,,C3553407,,614671,MONDO:0013847,chromosome 16p11.2 duplication syndrome,
+BMGC_DS14710,BMG_DS055928,,"CARDIOMYOPATHY, DILATED, 2B",,,,,,,C3553409,,614518;614672,MONDO:0013848,dilated cardiomyopathy 2B,
+BMGC_DS14711,BMG_DS055929,,"MICROCEPHALY 8, PRIMARY, AUTOSOMAL RECESSIVE",,,,,DOID:0070282,primary autosomal recessive microcephaly 8,C3553414,,611423;614673,MONDO:0013849,"microcephaly 8, primary, autosomal recessive",
+BMGC_DS14712,BMG_DS055930,1169366007,Menstrual cycle dependent periodic fever,,,,,,,C3553418,,614674,MONDO:0044660,menstrual cycle-dependent periodic fever,Luteal phase dependent febrile episode | Luteal phase dependent periodic fever | Menstrual cycle dependent periodic fever (disorder) | Menstrual cycle dependent febrile episode | Menstrual cycle dependent periodic fever
+BMGC_DS14713,BMG_DS055932,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21",,,,,DOID:0110311,hypertrophic cardiomyopathy 21,C3553442,,614676,MONDO:0013852,hypertrophic cardiomyopathy 21,
+BMGC_DS14714,BMG_DS055933,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 1B",,,,,DOID:0060266,pontocerebellar hypoplasia type 1B,C3553449,,606489;614678,MONDO:0013853,pontocerebellar hypoplasia type 1B,
+BMGC_DS14715,BMG_DS055934,,Profound global developmental delay,,,,,,,C3553450,,MTHU051054,,,
+BMGC_DS14716,BMG_DS055935,,,,,,,,,C3553462,,614680,MONDO:0013855,"influenza, severe, susceptibility to",
+BMGC_DS14717,BMG_DS055936,,"HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, IMPAIRED INTELLECTUAL DEVELOPMENT, AND RECURRENT INFLAMMATORY EPISODES",,,,,,,C3553465,,614684,MONDO:0013856,"hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, intellectual disability, and recurrent inflammatory episodes",
+BMGC_DS14718,BMG_DS055938,,"ALAR CLEFT, ISOLATED",,,,,,,C3553476,,614687,MONDO:0013857,"alar cleft, isolated",
+BMGC_DS14719,BMG_DS055939,,CATARACT 38,,,,,,,C3553494,,610345;614691,MONDO:0013859,cataract 38,
+BMGC_DS14720,BMG_DS055940,,"IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY",,,,,DOID:0081151,common variable immunodeficiency 8,C3553512,,614700;606453,MONDO:0013863,combined immunodeficiency due to LRBA deficiency,
+BMGC_DS14721,BMG_DS055941,,CORNELIA DE LANGE SYNDROME 4,,,,,,,C3553517,,614701;606462,MONDO:0013864,Cornelia de Lange syndrome 4,
+BMGC_DS14722,BMG_DS055942,,,,,,,,,C3553538,,614707,MONDO:0013867,Brown-Vialetto-van Laere syndrome 2,
+BMGC_DS14723,BMG_DS055943,,"POROKERATOSIS 7, MULTIPLE TYPES",,,,,,,C3553549,,603236;614714,MONDO:0013868,"porokeratosis 7, multiple types",
+BMGC_DS14724,BMG_DS055944,732252005,Carbohydrate deficient glycoprotein syndrome type 2k,,,,,,,C3553571,,614727,MONDO:0013870,TMEM165-congenital disorder of glycosylation,Carbohydrate deficient glycoprotein syndrome type 2k (disorder) | Carbohydrate deficient glycoprotein syndrome type 2k | Carbohydrate deficient glycoprotein syndrome type IIk | Congenital disorder of glycosylation type 2k | Congenital disorder of glycosylation type IIk | TMEM165-CDG - transmembrane protein 165 congenital disorder of glycosylation | Transmembrane protein 165 congenital disorder of glycosylation
+BMGC_DS14725,BMG_DS055945,,SECKEL SYNDROME 6,,,,,DOID:0070006,Seckel syndrome 6,C3553582,,614724;614728,MONDO:0013871,Seckel syndrome 6,
+BMGC_DS14726,BMG_DS055946,,GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY,,,,,,,C3553587,,607878;614736,MONDO:0013874,glucocorticoid deficiency 4,
+BMGC_DS14727,BMG_DS055947,,,,,,,,,C3553606,,614740,MONDO:0013876,"basal cell carcinoma, susceptibility to, 7",
+BMGC_DS14728,BMG_DS055948,1217212009,Mitochondrial pyruvate carrier deficiency,,,,,,,C3553607,,614741,MONDO:0013877,mitochondrial pyruvate carrier deficiency,Mitochondrial pyruvate carrier deficiency | Mitochondrial pyruvate carrier deficiency (disorder)
+BMGC_DS14729,BMG_DS055949,,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 1",,,,,,,C3553617,,187270;614742,MONDO:0013878,"pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1",
+BMGC_DS14730,BMG_DS055950,,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 2",,,,,,,C3553622,,614743;602322,MONDO:0013879,"pulmonary fibrosis and/or bone marrow failure, Telomere-related, 2",
+BMGC_DS14731,BMG_DS055951,,"FACIAL PARESIS, HEREDITARY CONGENITAL, 3",,,,,,,C3553625,,614744;142968,MONDO:0013880,"facial paresis, hereditary congenital, 3",
+BMGC_DS14732,BMG_DS055952,,HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 2,,,,,DOID:0070434,hyperphosphatasia with impaired intellectual development syndrome 2,C3553637,,614730;614749,MONDO:0013882,hyperphosphatasia with intellectual disability syndrome 2,
+BMGC_DS14733,BMG_DS055953,,"MYASTHENIC SYNDROME, CONGENITAL, 13",,,,,DOID:0110676,congenital myasthenic syndrome 13,C3553645,,191350;614750,MONDO:0013883,congenital myasthenic syndrome 13,
+BMGC_DS14734,BMG_DS055954,,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 12",,,,,DOID:0111205,autosomal dominant distal hereditary motor neuronopathy 12,C3553656,,614751;609139,MONDO:0013884,"neuronopathy, distal hereditary motor, type 5B",
+BMGC_DS14735,BMG_DS055955,763795006,Malan overgrowth syndrome,,,,,,,C3553660,,614753,MONDO:0013885,Malan overgrowth syndrome,Malan overgrowth syndrome | Sotos syndrome 2 | Malan overgrowth syndrome (disorder)
+BMGC_DS14736,BMG_DS055956,,CEREBELLAR DYSFUNCTION WITH VARIABLE COGNITIVE AND BEHAVIORAL ABNORMALITIES,,,,,DOID:0050998,nonprogressive cerebellar ataxia with mental retardation,C3553661,,614756;611501,MONDO:0013886,cerebellar dysfunction with variable cognitive and behavioral abnormalities,
+BMGC_DS14737,BMG_DS055957,,"HETEROTAXY, VISCERAL, 6, AUTOSOMAL",,,,,,,C3553676,,614779;614759,MONDO:0013887,"heterotaxy, visceral, 6, autosomal",
+BMGC_DS14738,BMG_DS055958,,AMYOTROPHIC LATERAL SCLEROSIS 18,,,,,DOID:0060209,amyotrophic lateral sclerosis type 18,C3553719,,614808;176610,MONDO:0013891,amyotrophic lateral sclerosis type 18,
+BMGC_DS14739,BMG_DS055959,,C3 GLOMERULOPATHY 3,,,,,,,C3553720,,608593;614809,,,
+BMGC_DS14740,BMG_DS055960,,,,,,,,,C3553728,,614810,MONDO:0013893,"multiple sclerosis, susceptibility to, 5",
+BMGC_DS14741,BMG_DS055961,,ADAMS-OLIVER SYNDROME 3,,,,,,,C3553748,,614814;147183,MONDO:0013895,Adams-Oliver syndrome 3,
+BMGC_DS14742,BMG_DS055962,,JOUBERT SYNDROME 18,,,,,DOID:0110987,Joubert syndrome 18,C3553758,,613847;614815,MONDO:0013896,Joubert syndrome 18,
+BMGC_DS14743,BMG_DS055963,,LOEYS-DIETZ SYNDROME 4,,,,,DOID:0070233,Loeys-Dietz syndrome 4,C3553762,,190220;614816,MONDO:0013897,Loeys-Dietz syndrome 4,
+BMGC_DS14744,BMG_DS055964,,"INTERSTITIAL NEPHRITIS, KARYOMEGALIC",,,,,,,C3553774,,614817;613534,MONDO:0013898,karyomegalic interstitial nephritis,
+BMGC_DS14745,BMG_DS055966,,WEILL-MARCHESANI SYNDROME 3,,,,,,,C3553785,,614819;602091,MONDO:0013899,Weill-Marchesani syndrome 3,
+BMGC_DS14746,BMG_DS055967,,ALTERNATING HEMIPLEGIA OF CHILDHOOD 2,,,,,,,C3553788,,182350;614820,MONDO:0013900,alternating hemiplegia of childhood 2,
+BMGC_DS14747,BMG_DS055968,,SPERMATOGENIC FAILURE 10,,,,,DOID:0070178,spermatogenic failure 10,C3553793,,614822,MONDO:0013901,spermatogenic failure 10,
+BMGC_DS14748,BMG_DS055969,,,,,,,,,C3553794,,,MONDO:0004983,spermatogenic failure,
+BMGC_DS14749,BMG_DS055970,,"NYSTAGMUS 7, CONGENITAL, AUTOSOMAL DOMINANT",,,,,DOID:0111791,congenital nystagmus 7,C3553801,,614826,MONDO:0013903,"nystagmus 7, congenital, autosomal dominant",
+BMGC_DS14750,BMG_DS055971,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8",,,,,DOID:0111231,congenital muscular dystrophy-dystroglycanopathy type A8,C3553813,,614828;614830,MONDO:0013904,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8",
+BMGC_DS14751,BMG_DS055972,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13",,,,,DOID:0080062,autosomal recessive spinocerebellar ataxia 13,C3553816,,604473;614831,MONDO:0013905,autosomal recessive spinocerebellar ataxia 13,
+BMGC_DS14752,BMG_DS055973,,"AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4",,,,,,,C3553830,,614829;614832,MONDO:0013906,amelogenesis imperfecta hypomaturation type 2A4,
+BMGC_DS14753,BMG_DS055974,,"MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES",,,,,,,C3553831,,614833,MONDO:0018764,microcephalic primordial dwarfism due to RTTN deficiency,
+BMGC_DS14754,BMG_DS055977,,HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA,,,,,,,C3553841,,614837,MONDO:0013910,hypogonadotropic hypogonadism 8 with or without anosmia,
+BMGC_DS14755,BMG_DS055978,,HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA,,,,,,,C3553842,,614838,MONDO:0013911,hypogonadotropic hypogonadism 9 with or without anosmia,
+BMGC_DS14756,BMG_DS055979,,HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA,,,,,,,C3553843,,162330;614839,MONDO:0013912,hypogonadotropic hypogonadism 10 with or without anosmia,
+BMGC_DS14757,BMG_DS055980,,HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA,,,,,,,C3553844,,614840,MONDO:0013913,hypogonadotropic hypogonadism 11 with or without anosmia,
+BMGC_DS14758,BMG_DS055981,,JOUBERT SYNDROME 19,,,,,DOID:0111122,nephronophthisis 14,C3553846,,604557;614844,MONDO:0800363,Joubert syndrome 19,
+BMGC_DS14759,BMG_DS055982,,TETRASOMY 15q26,,,,,,,C3553858,,614846,MONDO:0013918,distal tetrasomy 15q,
+BMGC_DS14760,BMG_DS055983,,,,,,,,,C3553859,,614847,MONDO:0013919,"epilepsy, idiopathic generalized, susceptibility to, 12",
+BMGC_DS14761,BMG_DS055984,,,,,,,,,C3553868,,614849,MONDO:0013920,"herpes simplex encephalitis, susceptibility to, 3",
+BMGC_DS14762,BMG_DS055985,,,,,,,,,C3553869,,614850,MONDO:0013921,"herpes simplex encephalitis, susceptibility to, 4",
+BMGC_DS14763,BMG_DS055986,,SECKEL SYNDROME 7,,,,,DOID:0070011,Seckel syndrome 7,C3553870,,614851;608684,MONDO:0013922,Seckel syndrome 7,
+BMGC_DS14764,BMG_DS055987,,"MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE",,,,,DOID:0070292,primary autosomal recessive microcephaly 9,C3553886,,614852;613529,MONDO:0013923,"microcephaly 9, primary, autosomal recessive",
+BMGC_DS14765,BMG_DS055988,,"OSTEOGENESIS IMPERFECTA, TYPE XIII",,,,,,,C3553887,,112264;614856,MONDO:0013924,osteogenesis imperfecta type 13,
+BMGC_DS14766,BMG_DS055989,,,,,,,,,C3553915,,614857,MONDO:0013925,"methylmalonic acidemia with homocystinuria, type cblJ",
+BMGC_DS14767,BMG_DS055990,,,,,,,,,C3553929,,614859,MONDO:0013927,peroxisome biogenesis disorder 3A (Zellweger),
+BMGC_DS14768,BMG_DS055991,,"DEAFNESS, AUTOSOMAL RECESSIVE 98",,,,,,,C3553932,,612920;614861,MONDO:0013929,autosomal recessive nonsyndromic hearing loss 98,
+BMGC_DS14769,BMG_DS055992,,,,,,,,,C3553936,,614862,MONDO:0013930,peroxisome biogenesis disorder 4A (Zellweger),
+BMGC_DS14770,BMG_DS055993,,PEROXISOME BIOGENESIS DISORDER 4B,,,,,DOID:0081433,Peroxisome biogenesis disorder 4B,C3553937,,601498;614863,MONDO:0013931,peroxisome biogenesis disorder 4B,
+BMGC_DS14771,BMG_DS055994,,,,,,,,,C3553940,,614866,MONDO:0013932,peroxisome biogenesis disorder 5A (Zellweger),
+BMGC_DS14772,BMG_DS055995,,"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 5",,,,,DOID:0080480,peroxisome biogenesis disorder 5A,C3553941,,614866,,,
+BMGC_DS14773,BMG_DS055996,,"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 10",,,,,DOID:0080480,peroxisome biogenesis disorder 5A,C3553942,,614866,,,
+BMGC_DS14774,BMG_DS055997,,IMMUNODEFICIENCY 110 WITH LYMPHOPROLIFERATION,,,,,,,C3553943,,604965;614868,MONDO:0013934,combined immunodeficiency due to STK4 deficiency,
+BMGC_DS14775,BMG_DS055998,,"USHER SYNDROME, TYPE IJ",,,,,,,C3553944,,605564;614869,MONDO:0013935,Usher syndrome type 1J,
+BMGC_DS14776,BMG_DS055999,,,,,,,,,C3553947,,614870,MONDO:0013936,peroxisome biogenesis disorder 6A (Zellweger),
+BMGC_DS14777,BMG_DS056000,,,,,,,,,C3553948,,614871,MONDO:0013937,peroxisome biogenesis disorder 6B,
+BMGC_DS14778,BMG_DS056001,,"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 8",,,,,DOID:0080482,peroxisome biogenesis disorder 7A,C3553950,,614872,,,
+BMGC_DS14779,BMG_DS056002,,,,,,,,,C3553951,,614873,MONDO:0013939,peroxisome biogenesis disorder 7B,
+BMGC_DS14780,BMG_DS056003,,METAPHYSEAL ENCHONDROMATOSIS WITH D-2-HYDROXYGLUTARIC ACIDURIA,,,,,,,C3553958,,614875,MONDO:0013941,metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria,
+BMGC_DS14781,BMG_DS056004,,,,,,,,,C3553959,,614876,MONDO:0013942,peroxisome biogenesis disorder 8A (Zellweger),
+BMGC_DS14782,BMG_DS056005,,,,,,,,,C3553960,,614877,MONDO:0013943,peroxisome biogenesis disorder 8B,
+BMGC_DS14783,BMG_DS056006,,"AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED",,,,,DOID:0070615,"autoinflammation, antibody deficiency, and immune dysregulation syndrome",C3553961,,614878,MONDO:0013944,autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation,
+BMGC_DS14784,BMG_DS056007,,HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA,,,,,,,C3553977,,614880,MONDO:0013946,hypogonadotropic hypogonadism 15 with or without anosmia,
+BMGC_DS14785,BMG_DS056010,,PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER),,,,,DOID:0080484,peroxisome biogenesis disorder 10A,C3553999,,603164;614882,MONDO:0013948,peroxisome biogenesis disorder 10A (Zellweger),
+BMGC_DS14786,BMG_DS056011,,PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER),,,,,DOID:0080485,peroxisome biogenesis disorder 11A,C3554000,,601789;614883,MONDO:0013949,peroxisome biogenesis disorder 11A (Zellweger),
+BMGC_DS14787,BMG_DS056012,,PEROXISOME BIOGENESIS DISORDER 11B,,,,,DOID:0081439,Peroxisome biogenesis disorder 11B,C3554001,,614885;601789,MONDO:0013950,peroxisome biogenesis disorder 11B,
+BMGC_DS14788,BMG_DS056013,,PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER),,,,,DOID:0080486,peroxisome biogenesis disorder 12A,C3554002,,600279;614886,MONDO:0013951,peroxisome biogenesis disorder 12A (Zellweger),
+BMGC_DS14789,BMG_DS056014,,PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER),,,,,DOID:0080487,peroxisome biogenesis disorder 13A,C3554004,,601791;614887,MONDO:0013952,peroxisome biogenesis disorder 13A (Zellweger),
+BMGC_DS14790,BMG_DS056015,,SINOATRIAL NODE DYSFUNCTION AND DEAFNESS,,,,,,,C3554018,,114206;614896,MONDO:0013960,sinoatrial node dysfunction and deafness,
+BMGC_DS14791,BMG_DS056016,,HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA,,,,,,,C3554021,,614897,MONDO:0013961,hypogonadotropic hypogonadism 16 with or without anosmia,
+BMGC_DS14792,BMG_DS056017,,DIAMOND-BLACKFAN ANEMIA 11,,,,,DOID:0111892,Diamond-Blackfan anemia 11,C3554042,,603704;614900,MONDO:0013964,Diamond-Blackfan anemia 11,
+BMGC_DS14793,BMG_DS056018,,LETHAL CONGENITAL CONTRACTURE SYNDROME 4,,,,,DOID:0060654,lethal congenital contracture syndrome 4,C3554046,,160794;614915,MONDO:0013965,lethal congenital contracture syndrome 4,
+BMGC_DS14794,BMG_DS056019,,"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4",,,,,,,C3554047,,114180;614916,MONDO:0013966,catecholaminergic polymorphic ventricular tachycardia 4,
+BMGC_DS14795,BMG_DS056020,,PEROXISOME BIOGENESIS DISORDER 14B,,,,,DOID:0081274,peroxisome biogenesis disorder 14B,C3554055,,603867;614920,MONDO:0013967,peroxisome biogenesis disorder 14B,
+BMGC_DS14796,BMG_DS056021,,BRANCHED-CHAIN KETO ACID DEHYDROGENASE KINASE DEFICIENCY,,,,,,,C3554078,,614923,MONDO:0013970,branched-chain keto acid dehydrogenase kinase deficiency,
+BMGC_DS14797,BMG_DS056022,,PERRAULT SYNDROME 2,,,,,,,C3554105,,614926;600783,MONDO:0013972,Perrault syndrome 2,
+BMGC_DS14798,BMG_DS056023,,"ECTODERMAL DYSPLASIA 5, HAIR/NAIL TYPE",,,,,DOID:0111657,ectodermal dysplasia 5,C3554108,,614927,MONDO:0013973,"ectodermal dysplasia 5, hair/nail type",
+BMGC_DS14799,BMG_DS056024,,"ECTODERMAL DYSPLASIA 6, HAIR/NAIL TYPE",,,,,DOID:0111659,ectodermal dysplasia 6,C3554111,,614928,MONDO:0013974,"ectodermal dysplasia 6, hair/nail type",
+BMGC_DS14800,BMG_DS056025,,"ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE",,,,,DOID:0111660,ectodermal dysplasia 7,C3554117,,608248;614929,MONDO:0013975,"ectodermal dysplasia 7, hair/nail type",
+BMGC_DS14801,BMG_DS056026,,"ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE",,,,,DOID:0111656,ectodermal dysplasia 9,C3554127,,142976;614931,MONDO:0013976,"ectodermal dysplasia 9, hair/nail type",
+BMGC_DS14802,BMG_DS056027,,"PALMOPLANTAR KERATODERMA, PUNCTATE TYPE IB",,,,,,,C3554145,,614936,MONDO:0013980,"palmoplantar keratoderma, punctate type ib",
+BMGC_DS14803,BMG_DS056028,,"DEAFNESS, AUTOSOMAL RECESSIVE 84B",,,,,,,C3554159,,614925;614944,MONDO:0013984,autosomal recessive nonsyndromic hearing loss 84B,
+BMGC_DS14804,BMG_DS056029,,"DEAFNESS, AUTOSOMAL RECESSIVE 18B",,,,,,,C3554163,,614945;604487,MONDO:0013985,autosomal recessive nonsyndromic hearing loss 18B,
+BMGC_DS14805,BMG_DS056030,,"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3",,,,,,,C3554194,,614954,MONDO:0013988,"congenital heart defects, multiple types, 3",
+BMGC_DS14806,BMG_DS056031,,,,,,,,,C3554195,,614959,MONDO:0013989,"developmental and epileptic encephalopathy, 14",
+BMGC_DS14807,BMG_DS056032,718611007,Congenital pontocerebellar hypoplasia type 8,,,,,,,C3554209,,614961,MONDO:0013990,pontocerebellar hypoplasia type 8,Congenital pontocerebellar hypoplasia type 8 (disorder) | Congenital pontocerebellar hypoplasia type 8 | PCH8 - pontocerebellar hypoplasia type 8 | Pontocerebellar hypoplasia type 8 | Pontocerebellar hypoplasia due to CHMP1A (charged multivesicular body protein 1A) mutation
+BMGC_DS14808,BMG_DS056033,,LEPTIN DEFICIENCY OR DYSFUNCTION,,,,,DOID:0111334,congenital leptin deficiency,C3554224,,614962,MONDO:0013991,obesity due to congenital leptin deficiency,
+BMGC_DS14809,BMG_DS056034,,LEPTIN RECEPTOR DEFICIENCY,,,,,,,C3554225,,614963;601007,MONDO:0013992,obesity due to leptin receptor gene deficiency,
+BMGC_DS14810,BMG_DS056035,718605009,Congenital pontocerebellar hypoplasia type 7,,,,,,,C3554226,,614969,MONDO:0013993,pontocerebellar hypoplasia type 7,Congenital pontocerebellar hypoplasia type 7 (disorder) | Congenital pontocerebellar hypoplasia type 7 | PCH7 - pontocerebellar hypoplasia type 7 | Pontocerebellar hypoplasia type 7
+BMGC_DS14811,BMG_DS056036,,JOUBERT SYNDROME 20,,,,,DOID:0110989,Joubert syndrome 20,C3554235,,614970;614949,MONDO:0013994,Joubert syndrome 20,
+BMGC_DS14812,BMG_DS056037,,"CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3",,,,,DOID:0070229,intrahepatic cholestasis of pregnancy 3,C3554241,,614972,MONDO:0013995,"cholestasis, intrahepatic, of pregnancy, 3",
+BMGC_DS14813,BMG_DS056038,,Focal Facial Dermal Dysplasia 2,Focal Facial Dermal Dysplasias,,,,,,C3554245,D000090303,614973,MONDO:0013996,focal facial dermal dysplasia type II,
+BMGC_DS14814,BMG_DS056039,,Focal Facial Dermal Dysplasia 4,Focal Facial Dermal Dysplasias,,,,,,C3554246,D000090303,614974,MONDO:0013997,focal facial dermal dysplasia type IV,
+BMGC_DS14815,BMG_DS056040,,CARPENTER SYNDROME 2,,,,,,,C3554247,,604267;614976,MONDO:0013998,MEGF8-related Carpenter syndrome,
+BMGC_DS14816,BMG_DS056041,,"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2",,,,,,,C3554279,,614980,MONDO:0014000,"congenital heart defects, multiple types, 2",
+BMGC_DS14817,BMG_DS056042,,"EPILEPSY, NOCTURNAL FRONTAL LOBE, 5",,,,,DOID:0060686,autosomal dominant nocturnal frontal lobe epilepsy 5,C3554306,,608167;615005,MONDO:0014002,autosomal dominant nocturnal frontal lobe epilepsy 5,
+BMGC_DS14818,BMG_DS056043,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 15,,,,,DOID:0080414,developmental and epileptic encephalopathy 15,C3554316,,606494;615006,MONDO:0014003,"developmental and epileptic encephalopathy, 15",
+BMGC_DS14819,BMG_DS056044,,"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4",,,,,,,C3554321,,615007;173410,MONDO:0014004,"basal ganglia calcification, idiopathic, 4",
+BMGC_DS14820,BMG_DS056045,,"NEPHROTIC SYNDROME, TYPE 7",,,,,DOID:0080388,nephrotic syndrome type 7,C3554330,,615008;601440,MONDO:0014005,immunoglobulin-mediated membranoproliferative glomerulonephritis,
+BMGC_DS14821,BMG_DS056046,,,,,,,,,C3554343,,615009,MONDO:0014006,Schuurs-Hoeijmakers syndrome,
+BMGC_DS14822,BMG_DS056047,,,,,,,,,C3554344,,615011,MONDO:0014008,phosphohydroxylysinuria,
+BMGC_DS14823,BMG_DS056048,,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 7",,,,,,,C3554348,,615022,MONDO:0014009,autosomal recessive congenital ichthyosis 7,
+BMGC_DS14824,BMG_DS056049,,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 9",,,,,,,C3554349,,615276;615023,MONDO:0014010,autosomal recessive congenital ichthyosis 9,
+BMGC_DS14825,BMG_DS056050,,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10",,,,,,,C3554355,,615024;612121,MONDO:0014011,autosomal recessive congenital ichthyosis 10,
+BMGC_DS14826,BMG_DS056051,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q",,,,,,,C3554366,,615025;614984,MONDO:0014012,Charcot-Marie-Tooth disease axonal type 2Q,
+BMGC_DS14827,BMG_DS056052,,"EPIDERMOLYSIS BULLOSA SIMPLEX 4, LOCALIZED OR GENERALIZED INTERMEDIATE, AUTOSOMAL RECESSIVE",,,,,,,C3554367,,615028;612878,MONDO:0014014,"epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive",
+BMGC_DS14828,BMG_DS056053,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND MACROCEPHALY,,,,,,,C3554373,,615032;610528,MONDO:0014017,intellectual developmental disorder with autism and macrocephaly,
+BMGC_DS14829,BMG_DS056054,783179009,Cranio-cervical dystonia with laryngeal and upper limb involvement,,,,,,,C3554374,,615034,MONDO:0014019,dystonia 24,Dystonia 24 | Cranio-cervical dystonia with laryngeal and upper limb involvement | DYT24 - dystonia 24 | Cranio-cervical dystonia with laryngeal and upper limb involvement (disorder)
+BMGC_DS14830,BMG_DS056055,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10",,,,,DOID:0111239,congenital muscular dystrophy-dystroglycanopathy type A10,C3554381,,605862;615041,MONDO:0014022,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10",
+BMGC_DS14831,BMG_DS056056,,"SPINAL MUSCULAR ATROPHY, JOKELA TYPE",,,,,DOID:0081356,"spinal muscular atrophy, Jokela type",C3554398,,615048;615903,MONDO:0014025,lower motor neuron syndrome with late-adult onset,
+BMGC_DS14832,BMG_DS056057,,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F",,,,,DOID:0110864,congenital stationary night blindness 1F,C3554399,,615004;615058,MONDO:0014026,congenital stationary night blindness 1F,
+BMGC_DS14833,BMG_DS056058,,HYPOTRICHOSIS 11,,,,,DOID:0110708,hypotrichosis 11,C3554409,,128260;615059,MONDO:0014027,hypotrichosis 11,
+BMGC_DS14834,BMG_DS056059,773396009,Distal arthrogryposis type 5D,,,,,,,C3554415,,615065,MONDO:0014028,distal arthrogryposis type 5D,Distal arthrogryposis type 5D (disorder) | Distal arthrogryposis type 5D | Distal arthrogryposis type 5 without ophthalmoparesis | Distal arthrogryposis type 5 without ophthalmoplegia | DA5D - distal arthrogryposis type 5D
+BMGC_DS14835,BMG_DS056060,,"OSTEOGENESIS IMPERFECTA, TYPE XIV",,,,,,,C3554428,,611236;615066,MONDO:0014029,osteogenesis imperfecta type 14,
+BMGC_DS14836,BMG_DS056061,770564004,Microcephalic primordial dwarfism Alazami type,,,,,,,C3554439,,615071,MONDO:0014031,"microcephalic primordial dwarfism, Alazami type",Microcephalic primordial dwarfism Alazami type (disorder) | Microcephalic primordial dwarfism Alazami type | Alazami syndrome
+BMGC_DS14837,BMG_DS056062,,"BRACHYDACTYLY, TYPE A1, C",,,,,DOID:0110977,brachydactyly type A1C,C3554446,,601146;615072,MONDO:0014032,brachydactyly type A1C,
+BMGC_DS14838,BMG_DS056063,,GAND SYNDROME,,,,,DOID:0070048,GAND syndrome,C3554448,,615074;614998,MONDO:0014034,severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome,
+BMGC_DS14839,BMG_DS056064,,NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS,,,,,DOID:0070049,autosomal dominant intellectual developmental disorder 19,C3554449,,615075;116806,MONDO:0014035,severe intellectual disability-progressive spastic diplegia syndrome,
+BMGC_DS14840,BMG_DS056065,,ALZHEIMER DISEASE 17,,,,,DOID:0110049,Alzheimer's disease 17,C3554452,,615080,MONDO:0014036,Alzheimer disease 17,
+BMGC_DS14841,BMG_DS056066,,SPERMATOGENIC FAILURE 11,,,,,DOID:0070180,spermatogenic failure 11,C3554453,,608778;615081,MONDO:0014037,spermatogenic failure 11,
+BMGC_DS14842,BMG_DS056067,,,,,,,,,C3554460,,615083,MONDO:0014038,"colorectal cancer, susceptibility to, 12",
+BMGC_DS14843,BMG_DS056068,,MITOCHONDRIAL DNA DEPLETION SYNDROME 11,,,,,DOID:0080129,mitochondrial DNA depletion syndrome 11,C3554462,,615076;615084,MONDO:0014039,mitochondrial DNA depletion syndrome 11,
+BMGC_DS14844,BMG_DS056069,,"OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8",,,,,DOID:0110940,autosomal recessive osteopetrosis 8,C3554478,,615085;614780,MONDO:0014040,autosomal recessive osteopetrosis 8,
+BMGC_DS14845,BMG_DS056070,,,,,,,,,C3554495,,615091,MONDO:0014041,"autism, susceptibility to, 19",
+BMGC_DS14846,BMG_DS056071,,LEFT VENTRICULAR NONCOMPACTION 7,,,,,,,C3554496,,608677;615092,MONDO:0014042,left ventricular noncompaction 7,
+BMGC_DS14847,BMG_DS056072,,"MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE",,,,,DOID:0070294,primary autosomal recessive microcephaly 10,C3554499,,610827;615095,MONDO:0014043,microcephalic primordial dwarfism due to ZNF335 deficiency,
+BMGC_DS14848,BMG_DS056073,,COWDEN SYNDROME 4,,,,,DOID:0081000,Cowden syndrome 4,C3554517,,612105;615107,MONDO:0014046,Cowden syndrome 4,
+BMGC_DS14849,BMG_DS056074,,COWDEN SYNDROME 5,,,,,DOID:0081001,Cowden syndrome 5,C3554518,,171834;615108,MONDO:0014047,Cowden syndrome 5,
+BMGC_DS14850,BMG_DS056075,,COWDEN SYNDROME 6,,,,,DOID:0081002,Cowden syndrome 6,C3554519,,164730;615109,MONDO:0014048,Cowden syndrome 6,
+BMGC_DS14851,BMG_DS056076,,UROFACIAL SYNDROME 2,,,,,,,C3554520,,608869;615112,MONDO:0014049,urofacial syndrome 2,
+BMGC_DS14852,BMG_DS056077,,"MICROPHTHALMIA, ISOLATED 8",,,,,,,C3554524,,615113;600463,MONDO:0014050,isolated microphthalmia 8,
+BMGC_DS14853,BMG_DS056078,,"CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2",,,,,DOID:0080358,mitochondrial complex IV deficiency nuclear type 6,C3554534,,615119,MONDO:0014051,"cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2",
+BMGC_DS14854,BMG_DS056079,,LYMPHOPROLIFERATIVE SYNDROME 2,,,,,,,C3554540,,615122;186711,MONDO:0014054,lymphoproliferative syndrome 2,
+BMGC_DS14855,BMG_DS056080,,"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 4",,,,,DOID:0111693,familial adult myoclonic epilepsy 4,C3554560,,615127;613373,MONDO:0014055,"epilepsy, familial adult myoclonic, 4",
+BMGC_DS14856,BMG_DS056082,,,,,,,,,C3554574,,615134,MONDO:0014056,"melanoma, cutaneous malignant, susceptibility to, 9",
+BMGC_DS14857,BMG_DS056083,,"MAPLE SYRUP URINE DISEASE, MILD VARIANT",,,,,,,C3554575,,615135;611065,MONDO:0014057,"maple syrup urine disease, mild variant",
+BMGC_DS14858,BMG_DS056084,,"FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE",,,,,,,C3554576,,174762;615139,MONDO:0014058,facial dysmorphism-immunodeficiency-livedo-short stature syndrome,
+BMGC_DS14859,BMG_DS056086,,MICROPHTHALMIA/COLOBOMA 9,,,,,,,C3554592,,610083;615145,MONDO:0014059,"microphthalmia, isolated, with coloboma 9",
+BMGC_DS14860,BMG_DS056087,,"RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME",,,,,,,C3554593,,615147;180250,MONDO:0014060,progressive retinal dystrophy due to retinol transport defect,
+BMGC_DS14861,BMG_DS056088,1197589000,Steel syndrome,,,,,,,C3554594,,615155,MONDO:0014061,Steel syndrome,"Bilateral hip and radial head dislocations, short stature, scoliosis, carpal coalition, pes cavus, facial dysmorphism syndrome | Bilateral hip and radial head dislocations, short stature, scoliosis, carpal coalition, pes cavus, facial dysmorphism syndrome (disorder) | Steel syndrome"
+BMGC_DS14862,BMG_DS056089,,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 6",,,,,DOID:0111519,autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6,C3554599,,601810;615156,MONDO:0014062,mitochondrial DNA deletion syndrome with progressive myopathy,
+BMGC_DS14863,BMG_DS056091,,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2",,,,,DOID:0060351,mitochondrial complex III deficiency nuclear type 2,C3554605,,613814;615157,MONDO:0014063,mitochondrial complex III deficiency nuclear type 2,
+BMGC_DS14864,BMG_DS056092,,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3",,,,,DOID:0080112,mitochondrial complex III deficiency nuclear type 3,C3554606,,191330;615158,MONDO:0014064,mitochondrial complex III deficiency nuclear type 3,
+BMGC_DS14865,BMG_DS056093,,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4",,,,,DOID:0080113,mitochondrial complex III deficiency nuclear type 4,C3554607,,612080;615159,MONDO:0014065,mitochondrial complex III deficiency nuclear type 4,
+BMGC_DS14866,BMG_DS056094,,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5",,,,,DOID:0080114,mitochondrial complex III deficiency nuclear type 5,C3554608,,191329;615160,MONDO:0014066,mitochondrial complex III deficiency nuclear type 5,
+BMGC_DS14867,BMG_DS056095,,,,,,,,,C3554609,,615162,MONDO:0014067,short ulna-dysmorphism-hypotonia-intellectual disability syndrome,
+BMGC_DS14868,BMG_DS056096,,CONE-ROD DYSTROPHY 17,,,,,DOID:0111023,cone-rod dystrophy 17,C3554610,,615163,MONDO:0014068,cone-rod dystrophy 17,
+BMGC_DS14869,BMG_DS056097,783553008,"Syndactyly, camptodactyly and clinodactyly of fifth fingers, bifid toes syndrome",,,,,,,C3554611,,615170,MONDO:0014069,syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome,"Syndactyly, camptodactyly and clinodactyly of fifth fingers, bifid toes syndrome (disorder) | Syndactyly, camptodactyly and clinodactyly of fifth fingers, bifid toes syndrome | Wahab syndrome | Synactyly, camptodactyly and clinodactyly of fifth fingers, bifid halluces syndrome"
+BMGC_DS14870,BMG_DS056098,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11",,,,,DOID:0111230,congenital muscular dystrophy-dystroglycanopathy type A11,C3554638,,615181;610194,MONDO:0014071,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11",
+BMGC_DS14871,BMG_DS056099,,"CARDIOMYOPATHY, DILATED, 1II",,,,,,,C3554649,,615184;123590,MONDO:0014073,dilated cardiomyopathy 1II,
+BMGC_DS14872,BMG_DS056100,,"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5",,,,,DOID:0070022,autosomal recessive dyskeratosis congenita 5,C3554656,,615190;608833,MONDO:0014076,"dyskeratosis congenita, autosomal recessive 5",
+BMGC_DS14873,BMG_DS056101,,LISSENCEPHALY 5,,,,,DOID:0112230,lissencephaly 5,C3554657,,615191;150240,MONDO:0014077,cobblestone lissencephaly without muscular or ocular involvement,
+BMGC_DS14874,BMG_DS056102,,"BLEEDING DISORDER, PLATELET-TYPE, 15",,,,,DOID:0111053,platelet-type bleeding disorder 15,C3554663,,615193;102575,MONDO:0014078,platelet-type bleeding disorder 15,
+BMGC_DS14875,BMG_DS056104,1237513008,Osteosclerotic metaphyseal dysplasia,,,,,,,C3554665,,615198,MONDO:0014080,osteosclerotic metaphyseal dysplasia,Osteosclerotic metaphyseal dysplasia | Osteosclerotic metaphyseal dysplasia (disorder)
+BMGC_DS14876,BMG_DS056105,,IMMUNODEFICIENCY 11,,,,,DOID:0111957,immunodeficiency 11A,C3554686,,615206,MONDO:0014081,severe combined immunodeficiency due to CARD11 deficiency,
+BMGC_DS14877,BMG_DS056106,,IMMUNODEFICIENCY 56,,,,,DOID:0111982,immunodeficiency 56,C3554687,,615207;605383,MONDO:0014082,cryptosporidiosis-chronic cholangitis-liver disease syndrome,
+BMGC_DS14878,BMG_DS056107,,"AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE",,,,,DOID:0081139,agammaglobulinemia 7,C3554689,,615214;171833,MONDO:0014083,"agammaglobulinemia 7, autosomal recessive",
+BMGC_DS14879,BMG_DS056108,,ATAXIA-OCULOMOTOR APRAXIA 3,,,,,DOID:0060557,ataxia with oculomotor apraxia type 3,C3554690,,615217;611317,MONDO:0014084,ataxia with oculomotor apraxia type 3,
+BMGC_DS14880,BMG_DS056109,,"HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES",,,,,,,C3554691,,615219,MONDO:0014085,"hydrocephalus, nonsyndromic, autosomal recessive 2",
+BMGC_DS14881,BMG_DS056111,763279007,"Facial dysmorphism, conductive hearing loss, heart defect syndrome",,,,,,,C3554774,,615102,MONDO:0014044,dysmorphism-conductive hearing loss-heart defect syndrome,"Facial dysmorphism, conductive hearing loss, heart defect syndrome | Tyshchenko syndrome | Facial dysmorphism, conductive hearing loss, heart defect syndrome (disorder) | Dysmorphism, conductive hearing loss, heart defect syndrome"
+BMGC_DS14882,BMG_DS056113,,,,,,,,,C3640086,,,MONDO:0020408,complete atrioventricular canal-tetralogy of fallot syndrome,
+BMGC_DS14883,BMG_DS056116,,,,,,,DOID:5843,posteroinferior myocardial infarction,C3642318,,,,,
+BMGC_DS14884,BMG_DS056117,,,,,,,DOID:5848,apical myocardial infarction,C3642319,,,MONDO:0003673,apical myocardial infarction,
+BMGC_DS14885,BMG_DS056119,,,,,,,DOID:4520,cervical endometrial stromal sarcoma,C3642326,,,MONDO:0003030,endometrioid stromal sarcoma of the cervix,
+BMGC_DS14886,BMG_DS056120,,,,,,,DOID:5170,vaginal endometrial stromal sarcoma,C3642329,,,MONDO:0003313,endometrioid stromal sarcoma of the vagina,
+BMGC_DS14887,BMG_DS056122,,,,,,,DOID:0060548,luminal breast carcinoma A,C3642345,,,MONDO:0021116,luminal A breast carcinoma,
+BMGC_DS14888,BMG_DS056123,,,,,,,DOID:0080674,luminal breast carcinoma B,C3642346,,,MONDO:0021115,luminal B breast carcinoma,
+BMGC_DS14889,BMG_DS056125,,,,,,,DOID:5851,posterolateral myocardial infarction,C3642463,,,,,
+BMGC_DS14890,BMG_DS056127,,,,,,,DOID:5849,subendocardial myocardial infarction,C3642476,,,,,
+BMGC_DS14891,BMG_DS056128,,Autosomal Recessive Centronuclear Myopathy,"Myopathies, Structural, Congenital",,,,,,C3645536,D020914,,MONDO:0015705,autosomal recessive centronuclear myopathy,
+BMGC_DS14892,BMG_DS056129,,Congenital Osteopetrosis,Osteopetrosis,,,,,,C3645711,D010022,,,,
+BMGC_DS14893,BMG_DS056153,,Drug-Induced Acute Liver Injury,Chemical and Drug Induced Liver Injury,,,,,,C3658290,D056486,,,,
+BMGC_DS14894,BMG_DS056154,,Hereditary Antithrombin Deficiency,Antithrombin III Deficiency,,,,,,C3658294,D020152,,,,
+BMGC_DS14895,BMG_DS056155,,Zellweger Spectrum,Zellweger Syndrome,,,,,,C3658299,D015211,,,,
+BMGC_DS14896,BMG_DS056156,,Mycoplasma-Induced Stevens-Johnson Syndrome,Stevens-Johnson Syndrome,,,,,,C3658301,D013262,,,,
+BMGC_DS14897,BMG_DS056157,,Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum,Stevens-Johnson Syndrome,,,,,,C3658302,D013262,,,,
+BMGC_DS14898,BMG_DS056164,,Partial Fetal Alcohol Syndrome,Fetal Alcohol Spectrum Disorders,,,,,,C3661483,D063647,,MONDO:0000393,partial fetal alcohol syndrome,
+BMGC_DS14899,BMG_DS056165,,Autosomal Dominant Myotubular Myopathy,"Myopathies, Structural, Congenital",,,,,,C3661489,D020914,,,,
+BMGC_DS14900,BMG_DS056166,,Hereditary Motor Neuronopathy,"Muscular Atrophy, Spinal",,,,,,C3661519,D009134,,,,
+BMGC_DS14901,BMG_DS056167,,Congenital Intestinal Aganglionosis,Hirschsprung Disease,,,,,,C3661523,D006627,,,,
+BMGC_DS14902,BMG_DS056168,,Autosomal Recessive Chronic Granulomatous Disease,"Granulomatous Disease, Chronic",,,,,,C3661525,D006105,,,,
+BMGC_DS14903,BMG_DS056207,434711000124103,Perioperative hypertension,,,,,,,C3661921,,,,,Perioperative hypertension | Perioperative hypertension (disorder)
+BMGC_DS14904,BMG_DS056210,761000119102,Dyslipidemia due to type 2 diabetes mellitus,,,,,,,C3661933,,,,,Diabetic dyslipidemia associated with type 2 diabetes mellitus | Dyslipidemia associated with type II diabetes mellitus | Dyslipidemia due to type 2 diabetes mellitus (disorder) | Dyslipidemia due to type 2 diabetes mellitus
+BMGC_DS14905,BMG_DS056232,,Peroneal Nerve Entrapment,Peroneal Neuropathies,,,,,,C3661995,D020427,,,,
+BMGC_DS14906,BMG_DS056240,,Radial Nerve Entrapment,Radial Neuropathy,,,,,,C3662011,D020425,,,,
+BMGC_DS14907,BMG_DS056250,771000119108,Chronic kidney disease due to type 2 diabetes mellitus,,,,,,,C3662038,,,,,Chronic renal impairment due to type II diabetes mellitus | Diabetic chronic renal impairment due to type 2 diabetes mellitus | Chronic kidney disease due to type 2 diabetes mellitus | Chronic renal impairment due to type 2 diabetes mellitus | Chronic kidney disease due to type 2 diabetes mellitus (disorder)
+BMGC_DS14908,BMG_DS056286,609536007,Dextran pseudoallergy,,,,,,,C3662114,,,,,Dextran pseudoallergy | Pseudoallergy to dextran | Nonallergic hypersensitivity to dextran | Non-allergic hypersensitivity to dextran (finding) | Non-allergic hypersensitivity to dextran
+BMGC_DS14909,BMG_DS056363,15471000;233873004;700065003,Primary hypertrophic cardiomyopathy,,,,,,,C3665332,,,,,Primary hypertrophic cardiomyopathy | Primary hypertrophic cardiomyopathy (disorder) | Hypertrophic cardiomyopathy | HCM - Hypertrophic cardiomyopathy | Hypertrophic cardiomyopathy (disorder) | Primary hypertrophic cardiomyopathy (disorder) | Primary hypertrophic cardiomyopathy
+BMGC_DS14910,BMG_DS056364,,Keratitis-Ichthyosis-Deafness Syndrome,,,,,,,C3665333,C580224,,MONDO:0018781,KID syndrome,
+BMGC_DS14911,BMG_DS056367,,Progressive Cone Dystrophy,Cone Dystrophy,,,,DOID:0050795,cone dystrophy,C3665342,D000077765,,,,
+BMGC_DS14912,BMG_DS056368,82598004,Secondary hypothyroidism,,,,,,,C3665349,,,,,Secondary hypothyroidism | Pituitary hypothyroidism | Hypothyrotropic hypothyroidism | Secondary hypothyroidism (disorder) | TSH (thyroid stimulating hormone) deficiency
+BMGC_DS14913,BMG_DS056369,155965001,Galactorrhea,Galactorrhea,,,,,,C3665358,D005687,,MONDO:0009256,galactorrhea,Galactorrhoea | Galactorrhea | Galactorrhoea (disorder)
+BMGC_DS14914,BMG_DS056370,39468009,"Arteriosclerotic cardiovascular disease, NOS",,,,,DOID:2348,arteriosclerotic cardiovascular disease,C3665365,,,,,Arteriosclerotic cardiovascular disease | Cardiovascular arteriosclerosis | ASCVD | Cardiovascular degeneration with arteriosclerosis | Cardiovascular disease with arteriosclerosis | Cardiovascular sclerosis with arteriosclerosis | Arteriosclerotic cardiovascular disease (disorder)
+BMGC_DS14915,BMG_DS056372,,"2,8-Dihydroxyadenine Urolithiasis",,,,,DOID:0060350,adenine phosphoribosyltransferase deficiency,C3665382,C538228,,,,
+BMGC_DS14916,BMG_DS056375,,Hemoglobin M Disease,,,,,,,C3665425,C581942,617971,MONDO:0018023,hemoglobin M disease,
+BMGC_DS14917,BMG_DS056382,,Familial Osteochondritis Dissecans,,,,,,,C3665488,C580095,165800,MONDO:0100462,"short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans",
+BMGC_DS14918,BMG_DS056387,,Warts,Warts,,,,,,C3665596,D014860,MTHU062503,MONDO:0001209,common wart,
+BMGC_DS14919,BMG_DS056391,,,,,,,DOID:3479,uveal cancer,C3665670,,,MONDO:0002659,uveal cancer,
+BMGC_DS14920,BMG_DS056392,234576008,Chronic familial neutropenia (disorder),,,,,,,C3665676,,162700,MONDO:0008089,"neutropenia, chronic familial",Chronic familial neutropaenia | Benign familial neutropaenia | Chronic familial neutropenia (disorder) | Benign familial neutropenia | Chronic familial neutropenia
+BMGC_DS14921,BMG_DS056393,703504006,Congenital reticular ichthyosiform erythroderma,,,,,,,C3665704,,609165,MONDO:0012208,congenital reticular ichthyosiform erythroderma,Congenital reticular ichthyosiform erythroderma (disorder) | Congenital reticular ichthyosiform erythroderma | Ichthyosis with confetti | Ichthyosis variegata | CRIE - Congenital reticular ichthyosiform erythroderma
+BMGC_DS14922,BMG_DS056401,,"Luteinizing Hormone Resistance, Female",,,,,DOID:0112259,Leydig cell hypoplasia,C3668935,C562567,,,,
+BMGC_DS14923,BMG_DS056402,,Dmd-Associated Dilated Cardiomyopathy,,,,,DOID:0110461,X-linked dilated cardiomyopathy,C3668940,C580047,302045,MONDO:0010542,dilated cardiomyopathy 3B,
+BMGC_DS14924,BMG_DS056403,,,,,,,,,C3668942,,108721,MONDO:0007168,atelosteogenesis type III,
+BMGC_DS14925,BMG_DS056404,,Fatty Acid Hydroxylase-Associated Neurodegeneration,,,,,,,C3668943,C580102,,MONDO:0017999,fatty acid hydroxylase-associated neurodegeneration,
+BMGC_DS14926,BMG_DS056406,,11-Beta-hydroxylase deficiency,,,,,,,C3669121,C535978,,,,
+BMGC_DS14927,BMG_DS056407,,5-Alpha Reductase Deficiency,,,,,,,C3669122,C535830,,,,
+BMGC_DS14928,BMG_DS056411,,X-Linked Chondrodysplasia Punctata 1,,,,,DOID:0060292,X-linked chondrodysplasia punctata 1,C3669395,C580533,302950,MONDO:0010555,X-linked chondrodysplasia punctata 1,
+BMGC_DS14929,BMG_DS056421,,Cyclic Hematopoesis,,,,,,,C3671688,C536227,,,,
+BMGC_DS14930,BMG_DS056424,,Autosomal Recessive Cerebellar Ataxia Type 1,,,,,,,C3683483,C579934,,,,
+BMGC_DS14931,BMG_DS056429,,,,,,,,,C3693482,,607907,MONDO:0011934,dermatofibrosarcoma protuberans,
+BMGC_DS14932,BMG_DS056431,,Middle East Respiratory Syndrome,Coronavirus Infections,,,,,,C3694279,D018352,,MONDO:0100116;MONDO:0005719,Coronavinae infectious disease | Middle East respiratory syndrome,
+BMGC_DS14933,BMG_DS056432,,GLYCOGEN STORAGE DISEASE IXa1,,,,,,,C3694531,,306000,MONDO:0010598,glycogen storage disease IXa1,
+BMGC_DS14934,BMG_DS056436,763345008,Charcot-Marie-Tooth disease type 4B3,,,,,,,C3695063,,615284,MONDO:0014117,Charcot-Marie-Tooth disease type 4B3,Charcot-Marie-Tooth disease type 4B3 | Charcot-Marie-Tooth disease with focally folded myelin | Charcot-Marie-Tooth disease type 4B3 (disorder)
+BMGC_DS14935,BMG_DS056440,,3-Methylglutaconic Aciduria,,,,,DOID:0060336,3-methylglutaconic aciduria,C3696376,C579867,,MONDO:0017359,3-methylglutaconic aciduria,
+BMGC_DS14936,BMG_DS056480,,Autosomal Dominant Nocturnal Frontal Lobe Epilepsy,,,,,DOID:0060681,autosomal dominant nocturnal frontal lobe epilepsy,C3696898,C579932,,MONDO:0020300,autosomal dominant nocturnal frontal lobe epilepsy,
+BMGC_DS14937,BMG_DS056495,697969008,Ulcerative colitis in remission,,,,,,,C3697010,,,,,Ulcerative colitis in remission | Ulcerative colitis in remission (disorder)
+BMGC_DS14938,BMG_DS056499,698296002,Acute exacerbation of chronic congestive heart failure,,,,,,,C3697063,,,,,Acute exacerbation of chronic congestive heart failure | Acute exacerbation of chronic congestive heart failure (disorder) | Acute on chronic congestive heart failure
+BMGC_DS14939,BMG_DS056505,697905000,Pulmonary arterial hypertension associated with congenital heart disease,,,,,,,C3697119,,,,,Pulmonary arterial hypertension associated with congenital heart disease | Pulmonary arterial hypertension associated with congenital heart disease (disorder)
+BMGC_DS14940,BMG_DS056557,698252002,Non-specific intraventricular conduction delay,,,,,,,C3697597,,,,,Non-specific intraventricular conduction delay | Non-specific intraventricular conduction defect | Non-specific intraventricular conduction delay (disorder) | Nonspecific intraventricular conduction disorder
+BMGC_DS14941,BMG_DS056670,699950009,Anti-D isoimmunization affecting pregnancy,,,,,,,C3698348,,,,,Anti-D isoimmunisation affecting pregnancy | Anti-D isoimmunization affecting pregnancy (disorder) | Anti-D isoimmunization affecting pregnancy
+BMGC_DS14942,BMG_DS056671,697909006,Pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis,,,,,,,C3698354,,,MONDO:0018554,pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis,Pulmonary veno-occlusive disease and/or pulmonary capillary hemangiomatosis (disorder) | Pulmonary veno-occlusive disease and/or pulmonary capillary hemangiomatosis | Pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis
+BMGC_DS14943,BMG_DS056708,,,,,,,DOID:0060263,porencephaly,C3698507,,,,,
+BMGC_DS14944,BMG_DS056715,699297004,"Ohdo syndrome, Maat-Kievit-Brunner type",,,,,,,C3698541,,300895,MONDO:0010477,"blepharophimosis - intellectual disability syndrome, MKB type","Ohdo syndrome, Maat-Kievit-Brunner type | Blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type | X-linked Ohdo syndrome | Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type (disorder) | Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type"
+BMGC_DS14945,BMG_DS056721,,Cap Myopathy,,,,,,,C3710589,C579969,,MONDO:0015753,cap myopathy,
+BMGC_DS14946,BMG_DS056723,,Mitochondrial DNA Depletion Syndrome 8A,,,,,DOID:0080127;DOID:0070331;DOID:0080119,mitochondrial DNA depletion syndrome 8b | mitochondrial DNA depletion syndrome 8a | mitochondrial DNA depletion syndrome 1,C3711125,C536350,,,,
+BMGC_DS14947,BMG_DS056725,,Metatropic Dysplasia Type 1,,,,,,,C3711162,C537356,,,,
+BMGC_DS14948,BMG_DS056726,,Surfactant Dysfunction,,,,,,,C3711368,C580477,,MONDO:0012580,hereditary pulmonary alveolar proteinosis,
+BMGC_DS14949,BMG_DS056727,,Succinate-Coa Ligase Deficiency,,,,,DOID:0080128,mitochondrial DNA depletion syndrome 9,C3711369,C580473,,,,
+BMGC_DS14950,BMG_DS056728,,Spastic Paraplegia Type 7,,,,,,,C3711370,C580457,,,,
+BMGC_DS14951,BMG_DS056730,,Nonsyndromic Deafness,,,,,DOID:0050563,nonsyndromic deafness,C3711374,C580334,,,,
+BMGC_DS14952,BMG_DS056731,,Isodicentric Chromosome 15 Syndrome,,,,,,,C3711376,C580205,,MONDO:0018027,duplication/inversion 15q11,
+BMGC_DS14953,BMG_DS056732,,Intranuclear Rod Myopathy,,,,,,,C3711377,C580202,,,,
+BMGC_DS14954,BMG_DS056734,,Huntington Disease-Like Syndrome,,,,,,,C3711380,C580174,,MONDO:0015548,Huntington disease-like syndrome,
+BMGC_DS14955,BMG_DS056735,,Hereditary Diffuse Leukoencephalopathy with Spheroids,,,,,,,C3711381,C580150,,MONDO:0030796,"leukoencephalopathy, hereditary diffuse, with spheroids",
+BMGC_DS14956,BMG_DS056737,,"Distal Hereditary Motor Neuropathy, Type II",,,,,DOID:0111206,autosomal dominant distal hereditary motor neuronopathy 2,C3711384,C580044,,MONDO:0015352,distal hereditary motor neuropathy type 2,
+BMGC_DS14957,BMG_DS056738,,Deoxyguanosine Kinase Deficiency,,,,,DOID:0080121,mitochondrial DNA depletion syndrome 3,C3711385,C580039,,MONDO:0100512,"mitochondrial DNA depletion syndrome, hepatocerebral form",
+BMGC_DS14958,BMG_DS056740,,Autosomal Recessive Primary Microcephaly,,,,,,,C3711387,C579935,,MONDO:0016660,autosomal recessive primary microcephaly,
+BMGC_DS14959,BMG_DS056742,,Actin-Accumulation Myopathy,,,,,,,C3711389,C579880,161800,MONDO:0008070,"congenital myopathy 2a, typical, autosomal dominant",
+BMGC_DS14960,BMG_DS056743,,9q22.3 Microdeletion,,,,,,,C3711390,C579873,,MONDO:0019179,monosomy 9q22.3,
+BMGC_DS14961,BMG_DS056745,,"Hdl Deficiency, Type 2",,,,,,,C3711531,C538394,,,,
+BMGC_DS14962,BMG_DS056746,,X-Linked Csnb,,,,,,,C3711543,C536122,,,,
+BMGC_DS14963,BMG_DS056750,726021008;237999008,Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency,,,,,,,C3711645,,609016,MONDO:0012173,long chain 3-hydroxyacyl-CoA dehydrogenase deficiency,Long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder) | Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | LCHADD - long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency | Long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency | Mitochondrial trifunctional protein deficiency | Human trifunctional protein deficiency | Trifunctional protein deficiency | Trifunctional enzyme deficiency | Mitochondrial trifunctional protein deficiency (disorder)
+BMGC_DS14964,BMG_DS056754,,Familial Hyperaldosteronism,,,,,,,C3713420,C580087,,MONDO:0016525,familial hyperaldosteronism,
+BMGC_DS14965,BMG_DS056755,,Childhood Myocerebrohepatopathy Spectrum,,,,,,,C3713421,C579990,,,,
+BMGC_DS14966,BMG_DS056757,,"46,XY Disorder of Sex Development Due To LH Defects",,,,,DOID:0112259,Leydig cell hypoplasia,C3714042,C562567,,,,
+BMGC_DS14967,BMG_DS056758,719909009,Trisomy Xq28,,,,,,,C3714043,C537723,,,,Chromosome Xq28 trisomy (disorder) | Chromosome Xq28 trisomy | Trisomy Xq28
+BMGC_DS14968,BMG_DS056759,,"Blepharophimosis, Ptosis, and Epicanthus Inversus Type II",,,,,,,C3714208,C562419,,,,
+BMGC_DS14969,BMG_DS056760,,"Trifunctional Protein Deficiency, Type 2",,,,,,,C3714237,C566945,,,,
+BMGC_DS14970,BMG_DS056761,,Bmpr1a-Related Juvenile Polyposis,,,,,DOID:0050787,juvenile polyposis syndrome,C3714239,C537702,,,,
+BMGC_DS14971,BMG_DS056762,,Smad4-Related Juvenile Polyposis,,,,,DOID:0050787,juvenile polyposis syndrome,C3714240,C537702,,,,
+BMGC_DS14972,BMG_DS056772,,Meckel syndrome type 1,,,,,,,C3714506,C536133,249000,MONDO:0009571,"Meckel syndrome, type 1",
+BMGC_DS14973,BMG_DS056773,,Nutrition Disorders,Nutrition Disorders,,,,DOID:374,nutrition disease,C3714509,D009748,,MONDO:0005137,nutritional disorder,
+BMGC_DS14974,BMG_DS056776,,,,,,,,,C3714524,,,MONDO:0019202,myxofibrosarcoma,
+BMGC_DS14975,BMG_DS056777,,,,,,,DOID:0060256,Dowling-Degos disease,C3714534,,,MONDO:0008371,Dowling-Degos disease,
+BMGC_DS14976,BMG_DS056779,,,,,,,,,C3714580,,170400,MONDO:0042979,"hypokalemic periodic paralysis, type 1",
+BMGC_DS14977,BMG_DS056780,,Multicystic Dysplastic Kidney,Multicystic Dysplastic Kidney,,,,,,C3714581,D021782,,MONDO:0015988,multicystic dysplastic kidney,
+BMGC_DS14978,BMG_DS056783,,Primary Hyperthyroidism,Hyperthyroidism,,,,DOID:7998,hyperthyroidism,C3714618,D006980,,,,
+BMGC_DS14979,BMG_DS056786,205237003,Pneumonitis,Pneumonia,,,,,,C3714636,D011014,MTHU065027,MONDO:0043905,pneumonitis,Pneumonitis | Pneumonitis (disorder)
+BMGC_DS14980,BMG_DS056787,,,,,,,,,C3714644,,,MONDO:0005197,thymus neoplasm,
+BMGC_DS14981,BMG_DS056791,,,,,,,,,C3714739,,,MONDO:0006856,mesothelial neoplasm,
+BMGC_DS14982,BMG_DS056793,,"RETINOSCHISIS 1, X-LINKED, JUVENILE",,,,,,,C3714753,,300839;312700,MONDO:0010725,X-linked retinoschisis,
+BMGC_DS14983,BMG_DS056794,,,,,,,,,C3714756,,,MONDO:0001071,intellectual disability,
+BMGC_DS14984,BMG_DS056795,201808003;156483006;268052008;410795001;86119004;239801005,Juvenile rheumatoid arthritis,,,,,,,C3714757,,,,,Juvenile rheumatoid arthritis | Juvenile rheumatoid arthritis (disorder) | Juvenile rheumatoid arthritis &/or Still's disease | Still's disease | Still's disease - juvenile R.A | Juvenile rheumatoid arthritis | Juvenile rheumatoid a. | Juvenile rheumatoid arthritis &/or Still's disease (disorder) | Juvenile rheumatoid arthritis &/or Still's disease | Juvenile rheumatoid arthritis | Still's disease | Juvenile rheumatoid a. | Still's disease - juvenile R.A | Juvenile rheumatoid arthritis &/or Still's disease (disorder) | Juvenile rheumatoid arthritis (disorder) | Juvenile rheumatoid arthritis | JRA - Juvenile rheumatoid arthritis | Polyarticular juvenile rheumatoid arthritis | Polyarticular juvenile rheumatoid arthritis (disorder) | Juvenile rheumatoid arthritis | Juvenile seropositive arthritis | JRA - Juvenile rheumatoid arthritis | Juvenile rheumatoid arthritis (disorder)
+BMGC_DS14985,BMG_DS056796,239802003,Juvenile psoriatic arthritis,,,,,,,C3714758,,,MONDO:0019436,psoriasis-related juvenile idiopathic arthritis,Juvenile psoriatic arthritis | Juvenile psoriatic arthritis (disorder)
+BMGC_DS14986,BMG_DS056797,102449007,Drug-induced tardive dyskinesia,,,,,,,C3714760,,,,,Tardive dyskinesia | Tardive dyskinesia (disorder) | Drug-induced tardive dyskinesia | TD - Tardive dyskinesia
+BMGC_DS14987,BMG_DS056799,,"Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia",Familial Primary Pulmonary Hypertension,,,,,,C3714844,D065627,,,,
+BMGC_DS14988,BMG_DS056800,,"Axenfeld-Rieger Syndrome, Type 1",,,,,,,C3714873,C535679,180500,MONDO:0008386,Axenfeld-Rieger syndrome type 1,
+BMGC_DS14989,BMG_DS056801,,SMITH-MCCORT DYSPLASIA 2,,,,,DOID:0081271,Smith-McCort dysplasia 2,C3714896,,605950;615222,MONDO:0014087,Smith-McCort dysplasia 2,
+BMGC_DS14990,BMG_DS056802,,"SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE",,,,,,,C3714897,,602498;615658,MONDO:0014295,hereditary spastic paraplegia 57,
+BMGC_DS14991,BMG_DS056803,,"SYMPHALANGISM, PROXIMAL, 1A",,,,,DOID:0080787,proximal symphalangism 1,C3714899,,602991;185800,MONDO:0020733,proximal symphalangism 1A,
+BMGC_DS14992,BMG_DS056804,,,,,,,,,C3714927,,146500,MONDO:0020715,"multiple system atrophy 1, susceptibility to",
+BMGC_DS14993,BMG_DS056805,,MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY,,,,,,,C3714933,,102770;615511,MONDO:0014220,myopathy due to myoadenylate deaminase deficiency,
+BMGC_DS14994,BMG_DS056806,,"MYOPATHY, MYOFIBRILLAR, 3",,,,,,,C3714934,,604103;609200;182920;159000;609200,MONDO:0012215,myofibrillar myopathy 3,
+BMGC_DS14995,BMG_DS056807,,OTOFACIOCERVICAL SYNDROME 1,,,,,,,C3714941,,166780;601653,MONDO:0024532,otofaciocervical syndrome 1,
+BMGC_DS14996,BMG_DS056808,,OTOFACIOCERVICAL SYNDROME 2,,,,,,,C3714942,,167411,,,
+BMGC_DS14997,BMG_DS056809,,PACHYONYCHIA CONGENITA 3,,,,,,,C3714948,,615726;148041,MONDO:0014324,pachyonychia congenita 3,
+BMGC_DS14998,BMG_DS056810,,PACHYONYCHIA CONGENITA 4,,,,,,,C3714949,,615728;148042,MONDO:0014325,pachyonychia congenita 4,
+BMGC_DS14999,BMG_DS056811,,,,,,,,,C3714958,,615371,MONDO:0014151,"pulmonary hypertension, neonatal, susceptibility to",
+BMGC_DS15000,BMG_DS056812,,ACTIVATED PI3K-DELTA SYNDROME,,,,,DOID:0111936,immunodeficiency 14,C3714976,,615513,MONDO:0014222,immunodeficiency 14,
+BMGC_DS15001,BMG_DS056813,,BARDET-BIEDL SYNDROME 17,,,,,,,C3714980,,615994;606568,MONDO:0014445,Bardet-Biedl syndrome 17,
+BMGC_DS15002,BMG_DS056814,,"CANDIDIASIS, FAMILIAL, 8",,,,,,,C3714992,,615527;607043,MONDO:0014230,"candidiasis, familial, 8",
+BMGC_DS15003,BMG_DS056815,,"CARDIOMYOPATHY, DILATED, 1KK",,,,,,,C3714995,,608517;615248,MONDO:0014100,dilated cardiomyopathy 1KK,
+BMGC_DS15004,BMG_DS056816,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 22",,,,,,,C3714998,,608517;615248,,,
+BMGC_DS15005,BMG_DS056817,,"CEROID LIPOFUSCINOSIS, NEURONAL, 13 (KUFS TYPE)",,,,,,,C3715049,,615362;603539,MONDO:0014147,neuronal ceroid lipofuscinosis 13,
+BMGC_DS15006,BMG_DS056818,,CRANIOSYNOSTOSIS 3,,,,,DOID:0061011,craniosynostosis 3,C3715051,,600480;615314,MONDO:0014128,TCF12-related craniosynostosis,
+BMGC_DS15007,BMG_DS056819,,DEVELOPMENTAL DYSPLASIA OF THE HIP 2,,,,,DOID:0060932,developmental dysplasia of the hip 2,C3715079,,615612,MONDO:0014277,developmental dysplasia of the hip 2,
+BMGC_DS15008,BMG_DS056820,,"EPIDERMOLYSIS BULLOSA SIMPLEX 1D, GENERALIZED, INTERMEDIATE OR SEVERE, AUTOSOMAL RECESSIVE",,,,,,,C3715082,,601001,MONDO:0010976,"epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive",
+BMGC_DS15009,BMG_DS056821,,"HYPOCALCEMIA, AUTOSOMAL DOMINANT 1",,,,,DOID:0090107,autosomal dominant hypocalcemia 1,C3715128,,601199;601198,MONDO:0016983,Bartter syndrome with hypocalcemia,
+BMGC_DS15010,BMG_DS056823,,AMYOTROPHIC LATERAL SCLEROSIS 19,,,,,DOID:0060210,amyotrophic lateral sclerosis type 19,C3715155,,600543;615515,MONDO:0014223,amyotrophic lateral sclerosis type 19,
+BMGC_DS15011,BMG_DS056824,,AMYOTROPHIC LATERAL SCLEROSIS 20,,,,,DOID:0060211,amyotrophic lateral sclerosis type 20,C3715156,,164017;615426,MONDO:0014181,amyotrophic lateral sclerosis type 20,
+BMGC_DS15012,BMG_DS056825,,LEBER CONGENITAL AMAUROSIS 17,,,,,,,C3715164,,601147;615360,MONDO:0014145,Leber congenital amaurosis 17,
+BMGC_DS15013,BMG_DS056826,,LEFT VENTRICULAR NONCOMPACTION 10,,,,,DOID:0081158,dilated cardiomyopathy 1MM,C3715165,,615396;600958,MONDO:0014163,left ventricular noncompaction 10,
+BMGC_DS15014,BMG_DS056827,,,,,,,,,C3715192,,615381,MONDO:0014157,mandibular hypoplasia-deafness-progeroid syndrome,
+BMGC_DS15015,BMG_DS056828,,RENAL-HEPATIC-PANCREATIC DYSPLASIA 1,,,,,,,C3715199,,208540;608002,MONDO:0008833,renal-hepatic-pancreatic dysplasia 1,
+BMGC_DS15016,BMG_DS056829,,RETINITIS PIGMENTOSA 66,,,,,,,C3715216,,180290;615233,MONDO:0014093,retinitis pigmentosa 66,
+BMGC_DS15017,BMG_DS056836,,CATARACT 13 WITH ADULT i PHENOTYPE,,,,,,,C3805373,,116700;600429,MONDO:0007289,cataract 13 with adult I phenotype,
+BMGC_DS15018,BMG_DS056837,,"ALBINISM, OCULOCUTANEOUS, TYPE VI",,,,,DOID:0080614,oculocutaneous albinism type VI,C3805375,,113750;609802,MONDO:0018264,oculocutaneous albinism type 6,
+BMGC_DS15019,BMG_DS056838,,CATARACT 29,,,,,,,C3805409,,115800,MONDO:0007282,cataract 29,
+BMGC_DS15020,BMG_DS056839,,"CATARACT 20, MULTIPLE TYPES",,,,,,,C3805410,,116100;123730,,,
+BMGC_DS15021,BMG_DS056840,,CATARACT 30,,,,,,,C3805411,,193060;116300,MONDO:0007286,cataract 30,
+BMGC_DS15022,BMG_DS056841,,CATARACT 41,,,,,,,C3805412,,116400;606201,MONDO:0007287,cataract 41,
+BMGC_DS15023,BMG_DS056842,,"COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR IMPAIRED INTELLECTUAL DEVELOPMENT",,,,,,,C3805432,,606608;120433,MONDO:0007355,uveal coloboma-cleft lip and palate-intellectual disability,
+BMGC_DS15024,BMG_DS056843,,FOVEAL HYPOPLASIA 1,,,,,DOID:0070530,foveal hypoplasia 1,C3805604,,136520;607108,MONDO:0007628,foveal hypoplasia 1,
+BMGC_DS15025,BMG_DS056844,,"CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED",,,,,,,C3805618,,137440;176640,,,
+BMGC_DS15026,BMG_DS056851,,"MEGALENCEPHALY, AUTOSOMAL DOMINANT",,,,,,,C3805727,,155350,MONDO:0007961,"megalencephaly, autosomal dominant",
+BMGC_DS15027,BMG_DS056854,,"PRECOCIOUS PUBERTY, CENTRAL, 1",,,,,DOID:0112310,central precocious puberty 1,C3805879,,176400;604161,MONDO:0008302,central precocious puberty 1,
+BMGC_DS15028,BMG_DS056858,,"ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1",,,,,,,C3806153,,206100,MONDO:0008787,microcytic anemia with liver iron overload,
+BMGC_DS15029,BMG_DS056859,,BARDET-BIEDL SYNDROME 18,,,,,,,C3806174,,615995;613605,MONDO:0014446,Bardet-Biedl syndrome 18,
+BMGC_DS15030,BMG_DS056863,,"CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND IMPAIRED INTELLECTUAL DEVELOPMENT",,,,,,,C3806255,,219721,MONDO:0009062,cystic fibrosis-gastritis-megaloblastic anemia syndrome,
+BMGC_DS15031,BMG_DS056865,,DEAFNESS AND MYOPIA,,,,,DOID:0111628,high myopia-sensorineural deafness syndrome,C3806275,,609681;221200,MONDO:0009082,high myopia-sensorineural deafness syndrome,
+BMGC_DS15032,BMG_DS056872,,"MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE",,,,,,,C3806412,,612655;248000,MONDO:0009544,"macrocephaly/megalencephaly syndrome, autosomal recessive",
+BMGC_DS15033,BMG_DS056874,,"XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME",,,,,,,C3806565,,278760;133520,MONDO:0800313,"xeroderma pigmentosum, type F/Cockayne syndrome",
+BMGC_DS15034,BMG_DS056875,,"CONGENITAL SHORT BOWEL SYNDROME, X-LINKED",,,,,DOID:0080681,X-linked chronic idiopathic intestinal pseudo-obstruction,C3806579,,300048;300017,,,
+BMGC_DS15035,BMG_DS056876,,"DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION",,,,,DOID:0112123,"deafness, dystonia, and cerebral hypomyelination",C3806634,,300475;300398,MONDO:0010334,severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome,
+BMGC_DS15036,BMG_DS056878,,PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1,,,,,,,C3806670,,300818,MONDO:0010438,paroxysmal nocturnal hemoglobinuria 1,
+BMGC_DS15037,BMG_DS056879,771516000,Solute carrier family 35 member A2 congenital disorder of glycosylation,,,,,,,C3806688,,300896,MONDO:0010478,SLC35A2-congenital disorder of glycosylation,SLC35A2-CDG - solute carrier family 35 member A2 congenital disorder of glycosylation | Congenital disorder of glycosylation type 2m | Solute carrier family 35 member A2 congenital disorder of glycosylation (disorder) | Congenital disorder of glycosylation type IIm | Solute carrier family 35 member A2 congenital disorder of glycosylation | CDG2M - congenital disorder of glycosylation type 2m
+BMGC_DS15038,BMG_DS056880,,"CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6",,,,,,,C3806702,,300906;300905,MONDO:0010479,Charcot-Marie-Tooth disease X-linked dominant 6,
+BMGC_DS15039,BMG_DS056882,,,,,,,,,C3806711,,300909,MONDO:0100003,susceptibility to angioedema induced by ACE inhibitors,
+BMGC_DS15040,BMG_DS056883,,"PARKINSONISM WITH SPASTICITY, X-LINKED",,,,,DOID:0112105,X-linked parkinsonism-spasticity syndrome,C3806722,,300911;300556,MONDO:0010482,X-linked parkinsonism-spasticity syndrome,
+BMGC_DS15041,BMG_DS056884,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 98",,,,,DOID:0112044,non-syndromic X-linked intellectual disability 98,C3806730,,300912;300524,MONDO:0010483,"X-linked intellectual disability, Cantagrel type",
+BMGC_DS15042,BMG_DS056885,,"DEAFNESS, X-LINKED 6",,,,,DOID:0111740,X-linked deafness 6,C3806737,,300914;303631,MONDO:0010484,"hearing loss, X-linked 6",
+BMGC_DS15043,BMG_DS056886,,"MICROPHTHALMIA, SYNDROMIC 13",,,,,DOID:0111811,syndromic microphthalmia 13,C3806742,,300915;300193,MONDO:0010485,X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome,
+BMGC_DS15044,BMG_DS056887,,"OLMSTED SYNDROME, X-LINKED",,,,,DOID:0112012,X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques,C3806745,,300918;300294,MONDO:0010486,"Olmsted syndrome, X-linked",
+BMGC_DS15045,BMG_DS056888,,,,,,,,,C3806746,,300919,MONDO:0010487,"intellectual disability, X-linked 99",
+BMGC_DS15046,BMG_DS056889,,"GROWTH RETARDATION, PRENATAL, WITH PROGRESSIVE PANCYTOPENIA AND CEREBELLAR HYPOPLASIA",,,,,DOID:0070025,X-linked dyskeratosis congenita,C3806774,,305000,,,
+BMGC_DS15047,BMG_DS056891,,CRANIOSYNOSTOSIS 4,,,,,DOID:0061012,craniosynostosis 4,C3806917,,611888;600775,,,
+BMGC_DS15048,BMG_DS056892,,"DYSERYTHROPOIESIS, CONGENITAL, WITH ULTRASTRUCTURALLY NORMAL ERYTHROBLAST HETEROCHROMATIN",,,,,,,C3807235,,603529,MONDO:0011332,"Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin",
+BMGC_DS15049,BMG_DS056893,,"CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT",,,,,DOID:0050968,"autosomal dominant cerebellar ataxia, deafness and narcolepsy",C3807295,,604121;126375,MONDO:0011397,"autosomal dominant cerebellar ataxia, deafness and narcolepsy",
+BMGC_DS15050,BMG_DS056896,,"ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1",,,,,DOID:0110011,advanced sleep phase syndrome 1,C3807327,,604348;603426,MONDO:0011442,advanced sleep phase syndrome 1,
+BMGC_DS15051,BMG_DS056898,,AMYOTROPHIC LATERAL SCLEROSIS 21,,,,,DOID:0060212,amyotrophic lateral sclerosis type 21,C3807521,,164015;606070,MONDO:0011632,amyotrophic lateral sclerosis type 21,
+BMGC_DS15052,BMG_DS056899,,MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY,,,,,,,C3807541,,606369,,,
+BMGC_DS15053,BMG_DS056900,,"LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 7",,,,,,,C3807567,,601047;606721,MONDO:0011714,"partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome",
+BMGC_DS15054,BMG_DS056904,,CHROMOSOME 15q11.2 DUPLICATION SYNDROME,,,,,,,C3807826,,608636,,,
+BMGC_DS15055,BMG_DS056905,,FOVEAL HYPOPLASIA 2,,,,,,,C3807873,,609218;615585,MONDO:0012216,foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome,
+BMGC_DS15056,BMG_DS056907,,"CATARACT 23, MULTIPLE TYPES",,,,,,,C3808012,,610425,MONDO:0012489,cataract 23,
+BMGC_DS15057,BMG_DS056908,,CATARACT 11 WITH MICROPHTHALMIA AND NEURODEVELOPMENTAL ABNORMALITIES,,,,,,,C3808029,,610623,,,
+BMGC_DS15058,BMG_DS056910,,"CATARACT 33, MULTIPLE TYPES",,,,,,,C3808107,,611391,MONDO:0012665,cataract 33,
+BMGC_DS15059,BMG_DS056911,,"CATARACT 12, MULTIPLE TYPES",,,,,,,C3808115,,603212;611597,MONDO:0012701,cataract 12 multiple types,
+BMGC_DS15060,BMG_DS056912,,LEFT VENTRICULAR NONCOMPACTION 9,,,,,,,C3808145,,191010;611878,MONDO:0800346,left ventricular noncompaction 9,
+BMGC_DS15061,BMG_DS056913,,MICROTIA WITH OR WITHOUT HEARING IMPAIRMENT,,,,,,,C3808166,,604685;612290,,,
+BMGC_DS15062,BMG_DS056915,,"CHROMOSOME 17p13.3, CENTROMERIC, DUPLICATION SYNDROME",,,,,,,C3808300,,613215,MONDO:0013182,chromosome 17p13.3 duplication syndrome,
+BMGC_DS15063,BMG_DS056916,,"CATARACT 16, MULTIPLE TYPES",,,,,,,C3808377,,613763,MONDO:0013411,cataract 16 multiple types,
+BMGC_DS15064,BMG_DS056917,,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1",,,,,,,C3808397,,614039;602661,MONDO:0013541,complex cortical dysplasia with other brain malformations 1,
+BMGC_DS15065,BMG_DS056918,,PERRAULT SYNDROME 3,,,,,,,C3808414,,614129;601119,MONDO:0013588,Perrault syndrome 3,
+BMGC_DS15066,BMG_DS056919,,CHROMOSOME 2p16.3 DELETION SYNDROME,,,,,,,C3808494,,614332,MONDO:0013696,chromosome 2p16.3 deletion syndrome,
+BMGC_DS15067,BMG_DS056920,,BONE MARROW FAILURE SYNDROME 1,,,,,,,C3808553,,602122;614675,MONDO:0013851,autosomal dominant aplasia and myelodysplasia,
+BMGC_DS15068,BMG_DS056921,,IMMUNODEFICIENCY 32A,,,,,DOID:0111986,immunodeficiency 32A,C3808589,,601565;614893,MONDO:0013957,Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency,
+BMGC_DS15069,BMG_DS056923,,"EPISODIC PAIN SYNDROME, FAMILIAL, 1",,,,,DOID:0111729,familial episodic pain syndrome 1,C3808667,,604775;615040,MONDO:0014021,familial episodic pain syndrome with predominantly upper body involvement,
+BMGC_DS15070,BMG_DS056926,,"MYASTHENIC SYNDROME, CONGENITAL, 8",,,,,DOID:0110657,congenital myasthenic syndrome 8,C3808739,,615120;103320,MONDO:0014052,congenital myasthenic syndrome 8,
+BMGC_DS15071,BMG_DS056928,,"ALBINISM, OCULOCUTANEOUS, TYPE VII",,,,,DOID:0070100,oculocutaneous albinism type VII,C3808786,,614537;615179,MONDO:0014070,oculocutaneous albinism type 7,
+BMGC_DS15072,BMG_DS056929,,"CATARACT 39, MULTIPLE TYPES",,,,,,,C3808800,,123670;615188,MONDO:0014075,cataract 39 multiple types,
+BMGC_DS15073,BMG_DS056930,,"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 4",,,,,DOID:0070022,autosomal recessive dyskeratosis congenita 5,C3808802,,608833;615190,MONDO:0800366,"dyskeratosis congenita, autosomal dominant 4",
+BMGC_DS15074,BMG_DS056931,,"OSTEOGENESIS IMPERFECTA, TYPE XV",,,,,,,C3808844,,164820;615220,MONDO:0014086,osteogenesis imperfecta type 15,
+BMGC_DS15075,BMG_DS056932,,"ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2",,,,,DOID:0110012,advanced sleep phase syndrome 2,C3808874,,600864;615224,MONDO:0014088,advanced sleep phase syndrome 2,
+BMGC_DS15076,BMG_DS056933,,,,,,,,,C3808876,,616964;615225,MONDO:0014089,corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome,
+BMGC_DS15077,BMG_DS056934,,"POLYDACTYLY, POSTAXIAL, TYPE A6",,,,,,,C3808889,,194648;615226,MONDO:0014090,"polydactyly, postaxial, type A6",
+BMGC_DS15078,BMG_DS056935,,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4B",,,,,DOID:0070462,mitochondrial complex V (ATP synthase) deficiency nuclear type 4B,C3808899,,164360;615228,MONDO:0014091,mitochondrial complex V (ATP synthase) deficiency nuclear type 4B,
+BMGC_DS15079,BMG_DS056936,,,,,,,,,C3808913,,615232,MONDO:0014092,schizophrenia 18,
+BMGC_DS15080,BMG_DS056937,,"ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2",,,,,,,C3808920,,609671;615234,MONDO:0014094,severe congenital hypochromic anemia with ringed sideroblasts,
+BMGC_DS15081,BMG_DS056939,,"CARDIOMYOPATHY, DILATED, 1JJ",,,,,,,C3808935,,600133;615235,MONDO:0014095,dilated cardiomyopathy 1JJ,
+BMGC_DS15082,BMG_DS056940,1197749008,CIDEC-related familial partial lipodystrophy,,,,,,,C3808940,,615238,MONDO:0014098,CIDEC-related familial partial lipodystrophy,Cell death inducing DFFA like effector C-related familial partial lipodystrophy | CIDEC-related familial partial lipodystrophy | Cell death inducing DFFA like effector C-related familial partial lipodystrophy (disorder) | FPLD5 - familial partial lipodystrophy type 5
+BMGC_DS15083,BMG_DS056941,,"NEPHROTIC SYNDROME, TYPE 8",,,,,DOID:0080389,nephrotic syndrome type 8,C3808953,,601925;615244,MONDO:0014099,"nephrotic syndrome, type 8",
+BMGC_DS15084,BMG_DS056942,,"CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 4",,,,,,,C3808963,,615248;608517,,,
+BMGC_DS15085,BMG_DS056943,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12",,,,,DOID:0111235,congenital muscular dystrophy-dystroglycanopathy type A12,C3808964,,615249;615247,MONDO:0014101,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12",
+BMGC_DS15086,BMG_DS056944,,HYPOGONADOTROPIC HYPOGONADISM 17 WITH OR WITHOUT ANOSMIA,,,,,,,C3808971,,615266,MONDO:0014102,hypogonadotropic hypogonadism 17 with or without anosmia,
+BMGC_DS15087,BMG_DS056945,,HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA,,,,,,,C3808975,,615267,MONDO:0014103,hypogonadotropic hypogonadism 18 with or without anosmia,
+BMGC_DS15088,BMG_DS056946,,"CEREBELLAR ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSEQUILIBRIUM SYNDROME 4",,,,,DOID:0070559,"cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 4",C3808977,,605870;615268,MONDO:0014104,"cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 4",
+BMGC_DS15089,BMG_DS056947,,HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA,,,,,,,C3808981,,615269,MONDO:0014105,hypogonadotropic hypogonadism 19 with or without anosmia,
+BMGC_DS15090,BMG_DS056948,,HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA,,,,,,,C3808983,,615270,MONDO:0014106,hypogonadotropic hypogonadism 20 with or without anosmia,
+BMGC_DS15091,BMG_DS056949,,HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA,,,,,,,C3808986,,615271,MONDO:0014107,hypogonadotropic hypogonadism 21 with or without anosmia,
+BMGC_DS15092,BMG_DS056950,,"FANCONI ANEMIA, COMPLEMENTATION GROUP Q",,,,,DOID:0111093,Fanconi anemia complementation group Q,C3808988,,615272;133520,MONDO:0014108,Fanconi anemia complementation group Q,
+BMGC_DS15093,BMG_DS056951,,NGLY1 deficiency,,,,,DOID:0060728,congenital disorder of deglycosylation 1,C3808991,C000626124,,MONDO:0031376,congenital disorder of deglycosylation,
+BMGC_DS15094,BMG_DS056952,,"CATARACT 15, MULTIPLE TYPES",,,,,,,C3809001,,615274;154050,MONDO:0014110,cataract 15 multiple types,
+BMGC_DS15095,BMG_DS056953,,"CATARACT 19, MULTIPLE TYPES",,,,,,,C3809004,,615277,MONDO:0014111,cataract 19 multiple types,
+BMGC_DS15096,BMG_DS056954,,CARDIOFACIOCUTANEOUS SYNDROME 2,,,,,DOID:0111461,cardiofaciocutaneous syndrome 2,C3809005,,615278;190070,MONDO:0014112,cardiofaciocutaneous syndrome 2,
+BMGC_DS15097,BMG_DS056955,,CARDIOFACIOCUTANEOUS SYNDROME 3,,,,,DOID:0111462,cardiofaciocutaneous syndrome 3,C3809006,,615279;176872,MONDO:0014113,cardiofaciocutaneous syndrome 3,
+BMGC_DS15098,BMG_DS056956,,CARDIOFACIOCUTANEOUS SYNDROME 4,,,,,DOID:0111463,cardiofaciocutaneous syndrome 4,C3809007,,615280;601263,MONDO:0014114,cardiofaciocutaneous syndrome 4,
+BMGC_DS15099,BMG_DS056957,,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2",,,,,DOID:0090133,complex cortical dysplasia with other brain malformations 2,C3809013,,615282;604593,MONDO:0014116,complex cortical dysplasia with other brain malformations 2,
+BMGC_DS15100,BMG_DS056958,,"NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE",,,,,DOID:0112132,severe congenital neutropenia 5,C3809031,,615285;610035,MONDO:0014118,congenital neutropenia-myelofibrosis-nephromegaly syndrome,
+BMGC_DS15101,BMG_DS056960,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13",,,,,DOID:0111238,congenital muscular dystrophy-dystroglycanopathy type A13,C3809042,,615287;605517,MONDO:0014120,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13",
+BMGC_DS15102,BMG_DS056961,,"MYOFIBROMATOSIS, INFANTILE, 2",,,,,,,C3809084,,615293;600276,MONDO:0014122,"myofibromatosis, infantile, 2",
+BMGC_DS15103,BMG_DS056962,,"CILIARY DYSKINESIA, PRIMARY, 21",,,,,,,C3809087,,615294,MONDO:0014123,primary ciliary dyskinesia 21,
+BMGC_DS15104,BMG_DS056963,,ADAMS-OLIVER SYNDROME 4,,,,,,,C3809092,,615297;614789,MONDO:0014124,Adams-Oliver syndrome 4,
+BMGC_DS15105,BMG_DS056967,,"SYMPHALANGISM, PROXIMAL, 1B",,,,,DOID:0080788,proximal symphalangism 2,C3809104,,615298;601146,MONDO:0014125,"symphalangism, proximal, 1B",
+BMGC_DS15106,BMG_DS056968,,PERRAULT SYNDROME 4,,,,,,,C3809105,,615300;604544,MONDO:0014126,Perrault syndrome 4,
+BMGC_DS15107,BMG_DS056969,,DOWLING-DEGOS DISEASE 2,,,,,,,C3809147,,615327;607491,MONDO:0014130,Dowling-Degos disease 2,
+BMGC_DS15108,BMG_DS056970,773553003,"Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome",,,,,,,C3809160,,615328,MONDO:0014131,hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome,"Shaheen syndrome | Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome (disorder) | Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome"
+BMGC_DS15109,BMG_DS056971,1208620009,Multiple mitochondrial dysfunctions syndrome type 3,,,,,,,C3809165,,615330,MONDO:0014132,multiple mitochondrial dysfunctions syndrome 3,Multiple mitochondrial dysfunctions syndrome type 3 | MMDS3 - multiple mitochondrial dysfunctions syndrome type 3 | Multiple mitochondrial dysfunctions syndrome type 3 (disorder) | IBA57 (iron-sulfur cluster assembly factor IBA57) deficiency
+BMGC_DS15110,BMG_DS056972,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 16,,,,,DOID:0080449,developmental and epileptic encephalopathy 16,C3809173,,615338;138290;613577,MONDO:0014133,"developmental and epileptic encephalopathy, 16",
+BMGC_DS15111,BMG_DS056974,,"PULMONARY HYPERTENSION, PRIMARY, 3",,,,,,,C3809192,,615343;601047,MONDO:0014135,"pulmonary hypertension, primary, 3",
+BMGC_DS15112,BMG_DS056975,,"PULMONARY HYPERTENSION, PRIMARY, 4",,,,,,,C3809198,,603220;615344,MONDO:0014136,"pulmonary hypertension, primary, 4",
+BMGC_DS15113,BMG_DS056976,,Central precocious puberty 2,,,,,,,C3809199,C000726751,615346,MONDO:0014137,"precocious puberty, central, 2",
+BMGC_DS15114,BMG_DS056977,,NEMALINE MYOPATHY 8,,,,,DOID:0110930,nemaline myopathy 8,C3809209,,615340;615348,MONDO:0014138,nemaline myopathy 8,
+BMGC_DS15115,BMG_DS056978,1251499005,B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome,,,,,,,C3809210,,615349,MONDO:0014139,"Ehlers-Danlos syndrome, spondylodysplastic type, 2","Beta-1,3-galactosyltransferase 6-related spondylodysplastic Ehlers-Danlos syndrome | Beta-1,3-galactosyltransferase 6-related spondylodysplastic Ehlers-Danlos syndrome (disorder) | B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome | Ehlers-Danlos syndrome progeroid type 2"
+BMGC_DS15116,BMG_DS056979,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14",,,,,DOID:0111233,congenital muscular dystrophy-dystroglycanopathy A14,C3809216,,615350;615320,MONDO:0014140,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14",
+BMGC_DS15117,BMG_DS056980,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 14",,,,,DOID:0112377,muscular dystrophy-dystroglycanopathy type B14,C3809221,,615320;615351,MONDO:0014141,"muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14",
+BMGC_DS15118,BMG_DS056981,,NOONAN SYNDROME 8,,,,,,,C3809233,,609591;615355,MONDO:0014143,Noonan syndrome 8,
+BMGC_DS15119,BMG_DS056982,,"HYPOCALCEMIA, AUTOSOMAL DOMINANT 2",,,,,DOID:0090108,autosomal dominant hypocalcemia 2,C3809243,,139313;615361,MONDO:0014146,autosomal dominant hypocalcemia 2,
+BMGC_DS15120,BMG_DS056983,,ESTROGEN RESISTANCE,,,,,,,C3809250,,615363;133430,MONDO:0014148,estrogen resistance syndrome,
+BMGC_DS15121,BMG_DS056987,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94,,,,,DOID:0081325,developmental and epileptic encephalopathy 94,C3809278,,615369;602119,MONDO:0014150,developmental and epileptic encephalopathy 94,
+BMGC_DS15122,BMG_DS056988,,LEFT VENTRICULAR NONCOMPACTION 8,,,,,DOID:0081157,dilated cardiomyopathy 1LL,C3809288,,615373;605557,MONDO:0014152,left ventricular noncompaction 8,
+BMGC_DS15123,BMG_DS056989,,"CARDIOMYOPATHY, DILATED, 1LL",,,,,DOID:0081157,dilated cardiomyopathy 1LL,C3809289,,605557;615373,MONDO:0800367,"cardiomyopathy, dilated, 1LL",
+BMGC_DS15124,BMG_DS056990,,CONE-ROD DYSTROPHY 18,,,,,DOID:0111024,cone-rod dystrophy 18,C3809299,,612994;615374,MONDO:0014153,cone-rod dystrophy 18,
+BMGC_DS15125,BMG_DS056991,,"CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C",,,,,,,C3809309,,611101;615376,MONDO:0014154,Charcot-Marie-Tooth disease recessive intermediate C,
+BMGC_DS15126,BMG_DS056992,,"ATRIAL FIBRILLATION, FAMILIAL, 13",,,,,,,C3809311,,615377;600235,MONDO:0014155,"atrial fibrillation, familial, 13",
+BMGC_DS15127,BMG_DS056993,,"ATRIAL FIBRILLATION, FAMILIAL, 14",,,,,,,C3809312,,601327;615378,MONDO:0014156,"atrial fibrillation, familial, 14",
+BMGC_DS15128,BMG_DS056994,,NEPHRONOPHTHISIS 16,,,,,DOID:0111124,nephronophthisis 16,C3809320,,615370;615382,MONDO:0014158,nephronophthisis 16,
+BMGC_DS15129,BMG_DS056995,,IMMUNODEFICIENCY 7,,,,,DOID:0111977,immunodeficiency 7,C3809332,,186880;615387,MONDO:0014160,TCR-alpha-beta-positive T-cell deficiency,
+BMGC_DS15130,BMG_DS056997,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 16,,,,,DOID:0111469,combined oxidative phosphorylation deficiency 16,C3809339,,615395;611849,MONDO:0014162,infantile hypertrophic cardiomyopathy due to MRPL44 deficiency,
+BMGC_DS15131,BMG_DS056998,,"CARDIOMYOPATHY, DILATED, 1MM",,,,,DOID:0081158,dilated cardiomyopathy 1MM,C3809346,,600958;615396,MONDO:0800368,"cardiomyopathy, dilated, 1MM",
+BMGC_DS15132,BMG_DS057001,,"MECKEL SYNDROME, TYPE 11",,,,,,,C3809352,,615397;614949,MONDO:0014164,"Meckel syndrome, type 11",
+BMGC_DS15133,BMG_DS057002,,MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3,,,,,DOID:0080140,multiple congenital anomalies-hypotonia-seizures syndrome 3,C3809356,,615398;603530;615398;610272,MONDO:0014165,multiple congenital anomalies-hypotonia-seizures syndrome 3,
+BMGC_DS15134,BMG_DS057003,,PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2,,,,,,,C3809369,,615399,MONDO:0014166,paroxysmal nocturnal hemoglobinuria 2,
+BMGC_DS15135,BMG_DS057004,,"EPILEPSY, EARLY-ONSET, 5, WITH OR WITHOUT DEVELOPMENTAL DELAY",,,,,DOID:0111691,familial adult myoclonic epilepsy 5,C3809374,,615400,MONDO:0014167,"epilepsy, familial adult myoclonic, 5",
+BMGC_DS15136,BMG_DS057005,1229942009,Severe combined immunodeficiency due to CORO1A deficiency,,,,,,,C3809383,,615401,MONDO:0014168,severe combined immunodeficiency due to CORO1A deficiency,Severe combined immunodeficiency due to CORO1A deficiency | Severe combined immunodeficiency due to coronin 1A deficiency | Severe combined immunodeficiency due to coronin 1A deficiency (disorder)
+BMGC_DS15137,BMG_DS057006,,DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3,,,,,,,C3809394,,615402;605452,MONDO:0014169,dyschromatosis universalis hereditaria 3,
+BMGC_DS15138,BMG_DS057007,,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3",,,,,DOID:0090134,complex cortical dysplasia with other brain malformations 3,C3809414,,615411;602591,MONDO:0014170,complex cortical dysplasia with other brain malformations 3,
+BMGC_DS15139,BMG_DS057008,,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4",,,,,DOID:0090138,complex cortical dysplasia with other brain malformations 4,C3809420,,615412;191135,MONDO:0014171,complex cortical dysplasia with other brain malformations 4,
+BMGC_DS15140,BMG_DS057009,,SPERMATOGENIC FAILURE 12,,,,,DOID:0070171,spermatogenic failure 12,C3809427,,615413;608226,MONDO:0014172,spermatogenic failure 12,
+BMGC_DS15141,BMG_DS057010,,"MICROCEPHALY 11, PRIMARY, AUTOSOMAL RECESSIVE",,,,,DOID:0070287,primary autosomal recessive microcephaly 11,C3809431,,602978;615414,MONDO:0014173,"microcephaly 11, primary, autosomal recessive",
+BMGC_DS15142,BMG_DS057011,,RENAL-HEPATIC-PANCREATIC DYSPLASIA 2,,,,,,,C3809434,,615415;609799,MONDO:0014174,renal-hepatic-pancreatic dysplasia 2,
+BMGC_DS15143,BMG_DS057012,,"MITOCHONDRIAL DNA DEPLETION SYNDROME 12B (CARDIOMYOPATHIC TYPE), AUTOSOMAL RECESSIVE",,,,,DOID:0080335,mitochondrial DNA depletion syndrome 12b,C3809443,,615418;103220,MONDO:0014175,"mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive",
+BMGC_DS15144,BMG_DS057013,,"HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1",,,,,,,C3809454,,615419;611549,MONDO:0024567,"hypotonia, infantile, with psychomotor retardation and characteristic facies 1",
+BMGC_DS15145,BMG_DS057014,,"MYOPIA 22, AUTOSOMAL DOMINANT",,,,,,,C3809464,,615421;615420,MONDO:0014177,"myopia 22, autosomal dominant",
+BMGC_DS15146,BMG_DS057015,,INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2,,,,,DOID:0111384,inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2,C3809468,,615422,MONDO:0014178,inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2,
+BMGC_DS15147,BMG_DS057016,,INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3,,,,,DOID:0111386,inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3,C3809469,,615424,MONDO:0014179,inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3,
+BMGC_DS15148,BMG_DS057017,,"EPIDERMOLYSIS BULLOSA SIMPLEX 3, LOCALIZED OR GENERALIZED INTERMEDIATE, WITH BP230 DEFICIENCY",,,,,,,C3809470,,615425;113810,MONDO:0014180,"epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency",
+BMGC_DS15149,BMG_DS057018,,"MYOPIA 23, AUTOSOMAL RECESSIVE",,,,,,,C3809482,,615431;104225,MONDO:0014183,"myopia 23, autosomal recessive",
+BMGC_DS15150,BMG_DS057019,,SPECIFIC LANGUAGE IMPAIRMENT 5,,,,,,,C3809483,,615432;615404,MONDO:0014184,specific language impairment 5,
+BMGC_DS15151,BMG_DS057020,,CHROMOSOME 3q13.31 DELETION SYNDROME,,,,,,,C3809490,,615433,MONDO:0014185,chromosome 3q13.31 deletion syndrome,
+BMGC_DS15152,BMG_DS057021,,"AORTIC ANEURYSM, FAMILIAL THORACIC 8",,,,,,,C3809513,,615436;176894,MONDO:0014187,"aortic aneurysm, familial thoracic 8",
+BMGC_DS15153,BMG_DS057022,,INFANTILE LIVER FAILURE SYNDROME 1,,,,,DOID:0080717,infantile liver failure syndrome 1,C3809522,,151350;615438,MONDO:0024568,infantile liver failure syndrome 1,
+BMGC_DS15154,BMG_DS057023,,"MACULAR DEGENERATION, AGE-RELATED, 13",,,,,DOID:0110025,age related macular degeneration 13,C3809523,,615439,MONDO:0014189,age related macular degeneration 13,
+BMGC_DS15155,BMG_DS057024,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17,,,,,DOID:0111496,combined oxidative phosphorylation deficiency 17,C3809526,,605367;615440,MONDO:0014190,combined oxidative phosphorylation defect type 17,
+BMGC_DS15156,BMG_DS057025,,"CARDIAC ARRHYTHMIA SYNDROME, WITH OR WITHOUT SKELETAL MUSCLE WEAKNESS",,,,,,,C3809536,,615441,MONDO:0014191,catecholaminergic polymorphic ventricular tachycardia 5,
+BMGC_DS15157,BMG_DS057026,,"CILIARY DYSKINESIA, PRIMARY, 22",,,,,,,C3809543,,607070;615444,MONDO:0014192,primary ciliary dyskinesia 22,
+BMGC_DS15158,BMG_DS057027,,"CILIARY DYSKINESIA, PRIMARY, 23",,,,,,,C3809548,,615408;615451,MONDO:0014193,primary ciliary dyskinesia 23,
+BMGC_DS15159,BMG_DS057028,,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6",,,,,DOID:0080115,mitochondrial complex III deficiency nuclear type 6,C3809553,,123980;615453,MONDO:0014194,mitochondrial complex III deficiency nuclear type 6,
+BMGC_DS15160,BMG_DS057030,,"MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS",,,,,,,C3809567,,615458;607512,MONDO:0014195,microcornea-myopic chorioretinal atrophy,
+BMGC_DS15161,BMG_DS057031,,IMMUNODEFICIENCY 12,,,,,DOID:0111988,immunodeficiency 12,C3809583,,615468;604860,MONDO:0014197,combined immunodeficiency due to MALT1 deficiency,
+BMGC_DS15162,BMG_DS057032,765403009,FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome,,,,,,,C3809592,,615471,MONDO:0014198,mitochondrial DNA depletion syndrome 13,Mitochondrial DNA depletion syndrome 13 encephalomyopathic type | FBXL4-related early onset mitochondrial encephalopathy | FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome | FBXL4 (F-box and leucine rich repeat protein 4) related early onset mitochondrial encephalopathy | F-box and leucine rich repeat protein 4 related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form (disorder) | F-box and leucine rich repeat protein 4 related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form
+BMGC_DS15163,BMG_DS057033,,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17",,,,,DOID:0080450,developmental and epileptic encephalopathy 17,C3809606,,615473,MONDO:0014199,"developmental and epileptic encephalopathy, 17",
+BMGC_DS15164,BMG_DS057034,,"PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES",,,,,,,C3809609,,114206;615474,MONDO:0014200,aldosterone-producing adenoma with seizures and neurological abnormalities,
+BMGC_DS15165,BMG_DS057036,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 18,,,,,DOID:0080413,developmental and epileptic encephalopathy 18,C3809624,,615463;615476,MONDO:0014201,"developmental and epileptic encephalopathy, 18",
+BMGC_DS15166,BMG_DS057037,,"CILIARY DYSKINESIA, PRIMARY, 24",,,,,,,C3809634,,615481,MONDO:0014202,primary ciliary dyskinesia 24,
+BMGC_DS15167,BMG_DS057038,,"CILIARY DYSKINESIA, PRIMARY, 25",,,,,,,C3809641,,608706;615482,MONDO:0014203,primary ciliary dyskinesia 25,
+BMGC_DS15168,BMG_DS057039,,"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5",,,,,,,C3809645,,615483;190040,MONDO:0014204,"basal ganglia calcification, idiopathic, 5",
+BMGC_DS15169,BMG_DS057040,,INFANTILE LIVER FAILURE SYNDROME 2,,,,,,,C3809651,,608025;616483,MONDO:0014659,infantile liver failure syndrome 2,
+BMGC_DS15170,BMG_DS057041,,"MACULAR DEGENERATION, AGE-RELATED, 14",,,,,DOID:0110026,age related macular degeneration 14,C3809653,,615489,MONDO:0014207,age related macular degeneration 14,
+BMGC_DS15171,BMG_DS057042,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R",,,,,,,C3809655,,614141;615490,MONDO:0014208,Charcot-Marie-Tooth disease type 2R,
+BMGC_DS15172,BMG_DS057043,,"SPASTIC PARAPLEGIA 79B, AUTOSOMAL RECESSIVE",,,,,DOID:0112344,hereditary spastic paraplegia 79B,C3809665,,191342;615491,MONDO:0014209,early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome,
+BMGC_DS15173,BMG_DS057044,,,,,,,,,C3809672,,615493,MONDO:0014210,intellectual disability-hypotonia-spasticity-sleep disorder syndrome,
+BMGC_DS15174,BMG_DS057045,,"CILIARY DYSKINESIA, PRIMARY, 26",,,,,,,C3809684,,615500,MONDO:0014211,primary ciliary dyskinesia 26,
+BMGC_DS15175,BMG_DS057046,,,,,,,,,C3809686,,615502,MONDO:0014213,intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome,
+BMGC_DS15176,BMG_DS057047,,SHORT-RIB THORACIC DYSPLASIA 8 WITH OR WITHOUT POLYDACTYLY,,,,,,,C3809691,,615503;615462,MONDO:0014214,short-rib thoracic dysplasia 8 with or without polydactyly,
+BMGC_DS15177,BMG_DS057048,,"CILIARY DYSKINESIA, PRIMARY, 27",,,,,,,C3809701,,615504,MONDO:0014215,primary ciliary dyskinesia 27,
+BMGC_DS15178,BMG_DS057049,,"CILIARY DYSKINESIA, PRIMARY, 28",,,,,,,C3809706,,615505,MONDO:0014216,primary ciliary dyskinesia 28,
+BMGC_DS15179,BMG_DS057050,,"TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5",,,,,,,C3809710,,615506;605120,MONDO:0014217,"telangiectasia, hereditary hemorrhagic, type 5",
+BMGC_DS15180,BMG_DS057051,774211005,"Severe dermatitis, multiple allergies, metabolic wasting syndrome",,,,,,,C3809719,,615508,MONDO:0014218,severe dermatitis-multiple allergies-metabolic wasting syndrome,"Severe dermatitis, multiple allergies, metabolic wasting syndrome | Severe dermatitis, multiple allergies, metabolic wasting syndrome (disorder) | Congenital erythroderma, hypotrichosis, recurrent infections, multiple food allergies syndrome | SAM syndrome"
+BMGC_DS15181,BMG_DS057054,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 38",,,,,DOID:0081203,autosomal recessive intellectual developmental disorder 38,C3809753,,615516;605837,MONDO:0014224,developmental delay with autism spectrum disorder and gait instability,
+BMGC_DS15182,BMG_DS057055,,IMMUNODEFICIENCY 13,,,,,DOID:0111987,immunodeficiency 13,C3809768,,604011;615518,MONDO:0014226,idiopathic CD4 lymphocytopenia,
+BMGC_DS15183,BMG_DS057057,711154007,Cole disease,,,,,,,C3809781,,615522,MONDO:0014227,hypopigmentation-punctate palmoplantar keratoderma syndrome,Cole disease | Guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification | Guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification (disorder)
+BMGC_DS15184,BMG_DS057063,,"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 8",,,,,,,C3809798,,615523;615496,MONDO:0014228,"corneal dystrophy, Fuchs endothelial, 8",
+BMGC_DS15185,BMG_DS057064,,"MICROPHTHALMIA, SYNDROMIC 12",,,,,DOID:0111800,syndromic microphthalmia 12,C3809803,,615524;180220,MONDO:0014229,"microphthalmia, syndromic 12",
+BMGC_DS15186,BMG_DS057065,,"PARKINSON DISEASE 19A, JUVENILE-ONSET",,,,,,,C3809811,,615528;608375,MONDO:0014231,juvenile onset Parkinson disease 19A,
+BMGC_DS15187,BMG_DS057066,,,,,,,,,C3809819,,615529,MONDO:0014232,"craniosynostosis 5, susceptibility to",
+BMGC_DS15188,BMG_DS057067,,"PARKINSON DISEASE 20, EARLY-ONSET",,,,,DOID:0060898,Parkinson's disease 20,C3809824,,615530;604297,MONDO:0014233,early-onset Parkinson disease 20,
+BMGC_DS15189,BMG_DS057069,,CHROMOSOME 22q13 DUPLICATION SYNDROME,,,,,DOID:0060437,chromosome 22q13 duplication syndrome,C3809844,,615538,MONDO:0014235,chromosome 22q13 duplication syndrome,
+BMGC_DS15190,BMG_DS057070,,"EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2",,,,,DOID:0080737,Ehlers-Danlos syndrome musculocontractural type 2,C3809845,,605942;615539,MONDO:0014236,"Ehlers-Danlos syndrome, musculocontractural type 2",
+BMGC_DS15191,BMG_DS057071,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 39",,,,,DOID:0081204,autosomal recessive intellectual developmental disorder 39,C3809853,,614426;615541,MONDO:0014238,severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome,
+BMGC_DS15192,BMG_DS057072,,TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE,,,,,,,C3809858,,600576;615542,MONDO:0014239,testicular anomalies with or without congenital heart disease,
+BMGC_DS15193,BMG_DS057074,,PERIVENTRICULAR NODULAR HETEROTOPIA 6,,,,,,,C3809872,,615532;615544,MONDO:0014240,periventricular nodular heterotopia 6,
+BMGC_DS15194,BMG_DS057075,,,,,,,,,C3809874,,615545,MONDO:0014241,"leukemia, acute lymphoblastic, susceptibility to, 3",
+BMGC_DS15195,BMG_DS057076,,VAN MALDERGEM SYNDROME 2,,,,,DOID:0080586,Van Maldergem syndrome 2,C3809875,,612411;615546,MONDO:0014242,van Maldergem syndrome 2,
+BMGC_DS15196,BMG_DS057077,770680004,Prader-Willi-like syndrome,,,,,DOID:0111715,Schaaf-Yang syndrome,C3809877,,,MONDO:0018354,Prader-Willi-like syndrome,Prader-Willi-like syndrome | Prader-Willi-like syndrome (disorder)
+BMGC_DS15197,BMG_DS057078,783550006,Hereditary sensory and autonomic neuropathy type 7,,,,,,,C3809882,,615548,MONDO:0014244,hereditary sensory and autonomic neuropathy type 7,Hereditary sensory and autonomic neuropathy with hyperhidrosis and gastrointestinal dysfunction | Congenital insensitivity to pain with hyperhidrosis and gastrointestinal dysfunction | Hereditary sensory and autonomic neuropathy type 7 (disorder) | Hereditary sensory and autonomic neuropathy type 7 | Hereditary sensory and autonomic neuropathy type VII | HSAN7- hereditary sensory and autonomic neuropathy type 7
+BMGC_DS15198,BMG_DS057079,,DIAMOND-BLACKFAN ANEMIA 12,,,,,DOID:0111882,Diamond-Blackfan anemia 12,C3809888,,604174;615550,MONDO:0014245,Diamond-Blackfan anemia 12,
+BMGC_DS15199,BMG_DS057080,,"EPISODIC PAIN SYNDROME, FAMILIAL, 2",,,,,DOID:0111730,familial episodic pain syndrome 2,C3809893,,615551;604427,MONDO:0014246,"episodic pain syndrome, familial, 2",
+BMGC_DS15200,BMG_DS057081,,"EPISODIC PAIN SYNDROME, FAMILIAL, 3",,,,,DOID:0111731,familial episodic pain syndrome 3,C3809899,,615552;604385,MONDO:0014247,familial episodic pain syndrome with predominantly lower limb involvement,
+BMGC_DS15201,BMG_DS057082,,"ARTHROGRYPOSIS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES",,,,,,,C3809910,,605632;615553,MONDO:0014248,autism spectrum disorder - epilepsy - arthrogryposis syndrome,
+BMGC_DS15202,BMG_DS057083,,,,,,,,,C3809918,,615554,MONDO:0014249,multiple fibroadenoma of the breast,
+BMGC_DS15203,BMG_DS057084,,,,,,,,,C3809925,,615557,MONDO:0014251,"melioidosis, susceptibility to",
+BMGC_DS15204,BMG_DS057085,,"AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III",,,,,DOID:0110119,autoimmune lymphoproliferative syndrome type 3,C3809928,,615559;176977,MONDO:8000024,"autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD",
+BMGC_DS15205,BMG_DS057086,,COMPLEMENT FACTOR B DEFICIENCY,,,,,,,C3809950,,615561;138470,MONDO:0014255,complement factor b deficiency,
+BMGC_DS15206,BMG_DS057087,,RETINITIS PIGMENTOSA 67,,,,,,,C3809954,,615565;604043,MONDO:0014256,retinitis pigmentosa 67,
+BMGC_DS15207,BMG_DS057088,,"NEPHROTIC SYNDROME, TYPE 9",,,,,DOID:0080391,nephrotic syndrome type 9,C3809965,,615573;615567,MONDO:0014257,"nephrotic syndrome, type 9",
+BMGC_DS15208,BMG_DS057089,782757004,"Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome (disorder)",,,,,,,C3809971,,615574,MONDO:0014258,congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome,"Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Asparagine synthetase deficiency | Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome (disorder)"
+BMGC_DS15209,BMG_DS057090,,"IMMUNODEFICIENCY, COMMON VARIABLE, 10",,,,,DOID:0081152,common variable immunodeficiency 10,C3809991,,164012;615577,MONDO:0014260,"immunodeficiency, common variable, 10",
+BMGC_DS15210,BMG_DS057091,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18,,,,,DOID:0111484,combined oxidative phosphorylation deficiency 18,C3810001,,615564;615578,MONDO:0014261,growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome,
+BMGC_DS15211,BMG_DS057092,,RIENHOFF SYNDROME,,,,,DOID:0070236,Loeys-Dietz syndrome 5,C3810012,,615582,MONDO:0014262,Rienhoff syndrome,
+BMGC_DS15212,BMG_DS057093,1229895008,8q24.3 microdeletion syndrome,,,,,,,C3810023,,615583,MONDO:0014263,8q24.3 microdeletion syndrome,8q24.3 microdeletion syndrome (disorder) | Verheij syndrome | Deletion 8q24.3 | Monosomy 8q24.3 | 8q24.3 microdeletion syndrome
+BMGC_DS15213,BMG_DS057094,,ALZHEIMER DISEASE 18,,,,,DOID:0110050,Alzheimer's disease 18,C3810041,,615590,MONDO:0014265,Alzheimer disease 18,
+BMGC_DS15214,BMG_DS057095,,"MACULAR DEGENERATION, AGE-RELATED, 15",,,,,DOID:0110027,age related macular degeneration 15,C3810042,,615591,MONDO:0014266,age related macular degeneration 15,
+BMGC_DS15215,BMG_DS057096,,IMMUNODEFICIENCY 16,,,,,DOID:0111935,immunodeficiency 16,C3810053,,600315;615593,MONDO:0014268,combined immunodeficiency due to OX40 deficiency,
+BMGC_DS15216,BMG_DS057097,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19,,,,,DOID:0111476,combined oxidative phosphorylation deficiency 19,C3810055,,613311;615595,MONDO:0014269,combined oxidative phosphorylation deficiency 19,
+BMGC_DS15217,BMG_DS057098,733111000,Congenital disorder of glycosylation type 1w,,,,,,,C3810062,,,,,STT3A-CDG (congenital disorder of glycosylation) | Congenital disorder of glycosylation type 1w (disorder) | Congenital disorder of glycosylation type Iw | Congenital disorder of glycosylation type 1w
+BMGC_DS15218,BMG_DS057099,722205008,Palmoplantar keratoderma Nagashima type,,,,,DOID:0070555,Nagashima-type palmoplantar keratosis,C3810072,,615598,MONDO:0014272,"palmoplantar keratoderma, Nagashima type",Palmoplantar keratoderma Nagashima type (disorder) | Palmoplantar keratoderma Nagashima type
+BMGC_DS15219,BMG_DS057100,,"NEURODEVELOPMENTAL DISORDER WITH FEEDING DIFFICULTIES, THIN CORPUS CALLOSUM, AND FOOT DEFORMITY",,,,,DOID:0081205,autosomal recessive intellectual developmental disorder 40,C3810080,,615599;604912,MONDO:0014273,microcephaly-thin corpus callosum-intellectual disability syndrome,
+BMGC_DS15220,BMG_DS057101,1217208003,L-ferritin deficiency,,,,,,,C3810090,,615604,MONDO:0014274,L-ferritin deficiency,L-ferritin deficiency (disorder) | L-ferritin deficiency | LFTD - L-ferritin deficiency
+BMGC_DS15221,BMG_DS057103,,FANCONI RENOTUBULAR SYNDROME 3,,,,,DOID:0080759,Fanconi renotubular syndrome 3,C3810100,,607037;615605,MONDO:0014275,Fanconi renotubular syndrome 3,
+BMGC_DS15222,BMG_DS057104,,IMMUNODEFICIENCY 17,,,,,DOID:0111973,immunodeficiency 17,C3810107,,186740;615607,MONDO:0014276,combined immunodeficiency due to CD3gamma deficiency,
+BMGC_DS15223,BMG_DS057105,,IMMUNODEFICIENCY 18,,,,,DOID:0111971,immunodeficiency 18,C3810127,,186830;615615,MONDO:0014278,immunodeficiency 18,
+BMGC_DS15224,BMG_DS057106,,"IMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT",,,,,DOID:0111971,immunodeficiency 18,C3810128,,615615;186830,,,
+BMGC_DS15225,BMG_DS057107,,"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13",,,,,,,C3810138,,607667;615616,MONDO:0000908,arrhythmogenic right ventricular dysplasia 13,
+BMGC_DS15226,BMG_DS057108,,IMMUNODEFICIENCY 19,,,,,DOID:0111972,immunodeficiency 19,C3810147,,186790;615617,MONDO:0014280,immunodeficiency 19,
+BMGC_DS15227,BMG_DS057109,,,,,,,,,C3810156,,615619,MONDO:0014281,"cholangiocarcinoma, susceptibility to",
+BMGC_DS15228,BMG_DS057110,,"DEAFNESS, AUTOSOMAL DOMINANT 56",,,,,,,C3810170,,615629;187380,MONDO:0014283,autosomal dominant nonsyndromic hearing loss 56,
+BMGC_DS15229,BMG_DS057111,,SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY,,,,,,,C3810175,,607386;615630,MONDO:0014284,short-rib thoracic dysplasia 10 with or without polydactyly,
+BMGC_DS15230,BMG_DS057113,,"ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib",,,,,,,C3810185,,615626;615631,MONDO:0014285,congenital dyserythropoietic anemia type type 1B,
+BMGC_DS15231,BMG_DS057114,,"NEUROPATHY, HEREDITARY SENSORY, TYPE IF",,,,,DOID:0070154,hereditary sensory neuropathy type 1F,C3810194,,609369;615632,MONDO:0014286,"neuropathy, hereditary sensory, type 1F",
+BMGC_DS15232,BMG_DS057115,,SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY,,,,,,,C3810200,,615633;613363,MONDO:0014287,short-rib thoracic dysplasia 11 with or without polydactyly,
+BMGC_DS15233,BMG_DS057116,,JOUBERT SYNDROME 21,,,,,DOID:0110990,Joubert syndrome 21,C3810212,,615636;611654,MONDO:0014288,Joubert syndrome 21,
+BMGC_DS15234,BMG_DS057117,,,,,,,,,C3810225,,615637,MONDO:0014289,macrocephaly-developmental delay syndrome,
+BMGC_DS15235,BMG_DS057118,,WARBURG MICRO SYNDROME 4,,,,,,,C3810265,,611663;615663,MONDO:0014296,Warburg micro syndrome 4,
+BMGC_DS15236,BMG_DS057119,,JOUBERT SYNDROME 22,,,,,DOID:0110991,Joubert syndrome 22,C3810278,,602676;615665,MONDO:0014297,Joubert syndrome 22,
+BMGC_DS15237,BMG_DS057120,,CHROMOSOME 5q12 DELETION SYNDROME,,,,,DOID:0060421,chromosome 5q12 deletion syndrome,C3810282,,615668,MONDO:0014298,chromosome 5q12 deletion syndrome,
+BMGC_DS15238,BMG_DS057121,,SCHWANNOMATOSIS 2,,,,,,,C3810283,,615670;600574,MONDO:0014299,LZTR1-related schwannomatosis,
+BMGC_DS15239,BMG_DS057122,,MYOPATHY WITH EXTRAPYRAMIDAL SIGNS,,,,,DOID:0111335,myopathy with extrapyramidal signs,C3810285,,615673;605084,MONDO:0014300,proximal myopathy with extrapyramidal signs,
+BMGC_DS15240,BMG_DS057123,,DOWLING-DEGOS DISEASE 3,,,,,,,C3810286,,615674,MONDO:0014301,dowling-degos disease 3,
+BMGC_DS15241,BMG_DS057124,,"SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE",,,,,,,C3810289,,601752;615683,MONDO:0014303,hereditary spastic paraplegia 64,
+BMGC_DS15242,BMG_DS057125,,"SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE",,,,,,,C3810294,,607669;615685,MONDO:0014304,hereditary spastic paraplegia 61,
+BMGC_DS15243,BMG_DS057126,,"SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE",,,,,,,C3810295,,615686;102771,MONDO:0014305,hereditary spastic paraplegia 63,
+BMGC_DS15244,BMG_DS057127,,DOWLING-DEGOS DISEASE 4,,,,,,,C3810313,,615618;615696,MONDO:0014307,Dowling-Degos disease 4,
+BMGC_DS15245,BMG_DS057128,,"EPILEPSY, FAMILIAL TEMPORAL LOBE, 6",,,,,DOID:0060749,familial temporal lobe epilepsy 6,C3810320,,615697,MONDO:0014308,familial temporal lobe epilepsy 6,
+BMGC_DS15246,BMG_DS057129,,MORBID OBESITY AND SPERMATOGENIC FAILURE,,,,,,,C3810324,,615586;615703,MONDO:0014309,obesity due to CEP19 deficiency,
+BMGC_DS15247,BMG_DS057130,,"POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS",,,,,,,C3810325,,615584;615704,MONDO:0014310,hereditary sclerosing poikiloderma with tendon and pulmonary involvement,
+BMGC_DS15248,BMG_DS057131,782721009,"Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency (disorder)",,,,,,,C3810326,,615705,MONDO:0014311,autosomal recessive spinocerebellar ataxia 15,"Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN (RUN and cysteine rich domain containing beclin 1 interacting protein) deficiency | Autosomal recessive spinocerebellar ataxia type 15 | SCAR15 - autosomal recessive spinocerebellar ataxia type 15 | Salih ataxia | Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency (disorder) | Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency | Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUBCN deficiency"
+BMGC_DS15249,BMG_DS057132,,AURICULOCONDYLAR SYNDROME 3,,,,,,,C3810332,,131240;615706,MONDO:0014312,auriculocondylar syndrome 3,
+BMGC_DS15250,BMG_DS057133,,IMMUNODEFICIENCY 20,,,,,DOID:0111941,immunodeficiency 20,C3810342,,146740;615707,MONDO:0014313,autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity,
+BMGC_DS15251,BMG_DS057134,,SACRAL AGENESIS WITH VERTEBRAL ANOMALIES,,,,,,,C3810343,,601397;615709,MONDO:0014314,sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome,
+BMGC_DS15252,BMG_DS057135,,ALZHEIMER DISEASE 19,,,,,DOID:0110051,Alzheimer's disease 19,C3810349,,615711,MONDO:0014316,Alzheimer disease 19,
+BMGC_DS15253,BMG_DS057136,,BONE MARROW FAILURE SYNDROME 2,,,,,,,C3810350,,615715;615667,MONDO:0014317,pancytopenia-developmental delay syndrome,
+BMGC_DS15254,BMG_DS057137,,HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 4,,,,,DOID:0070436,hyperphosphatasia with impaired intellectual development syndrome 4,C3810354,,611801;615716,MONDO:0014318,hyperphosphatasia with intellectual disability syndrome 4,
+BMGC_DS15255,BMG_DS057138,,RENAL HYPODYSPLASIA/APLASIA 2,,,,,,,C3810359,,605558;615721,MONDO:0014319,renal hypodysplasia/aplasia 2,
+BMGC_DS15256,BMG_DS057139,770723007,"Optic atrophy, intellectual disability syndrome",,,,,,,C3810363,,615722,MONDO:0014320,Bosch-Boonstra-Schaaf optic atrophy syndrome,"Bosch Boonstra Schaaf optic atrophy syndrome | BBSOAS - Bosch Boonstra Schaaf optic atrophy syndrome | Optic atrophy, intellectual disability syndrome (disorder) | Optic atrophy, intellectual disability syndrome"
+BMGC_DS15257,BMG_DS057141,,PREMATURE OVARIAN FAILURE 8,,,,,DOID:0080865,primary ovarian insufficiency 8,C3810367,,608489;615723,MONDO:0014321,premature ovarian failure 8,
+BMGC_DS15258,BMG_DS057142,,PREMATURE OVARIAN FAILURE 9,,,,,DOID:0080866,primary ovarian insufficiency 9,C3810376,,615684;615724,MONDO:0014322,premature ovarian failure 9,
+BMGC_DS15259,BMG_DS057143,,RETINITIS PIGMENTOSA 68,,,,,,,C3810380,,615725;615720,MONDO:0014323,retinitis pigmentosa 68,
+BMGC_DS15260,BMG_DS057144,,NEMALINE MYOPATHY 9,,,,,DOID:0110929,nemaline myopathy 9,C3810384,,607701;615731,MONDO:0014326,nemaline myopathy 9,
+BMGC_DS15261,BMG_DS057145,,"PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL OR DIFFUSE",,,,,DOID:0111710,focal or diffuse nonepidermolytic palmoplantar keratoderma,C3810394,,615735,MONDO:0014327,"palmoplantar keratoderma, nonepidermolytic, focal or diffuse",
+BMGC_DS15262,BMG_DS057146,,,,,,,,,C3810400,,615744,MONDO:0014328,"developmental and epileptic encephalopathy, 19",
+BMGC_DS15263,BMG_DS057147,,ATRIAL STANDSTILL 2,,,,,DOID:0080663,atrial standstill 2,C3810401,,615745;108780,MONDO:0014329,atrial standstill 2,
+BMGC_DS15264,BMG_DS057148,,"ECULIZUMAB, POOR RESPONSE TO",,,,,,,C3810402,,615749;120900,,,
+BMGC_DS15265,BMG_DS057149,,MOYAMOYA DISEASE 6 WITH OR WITHOUT ACHALASIA,,,,,,,C3810403,,615750,MONDO:0014331,Moyamoya disease with early-onset achalasia,
+BMGC_DS15266,BMG_DS057150,,"CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO",,,,,,,C3810404,,615751;114761,MONDO:0014332,hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency,
+BMGC_DS15267,BMG_DS057151,,"POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE",,,,,DOID:0080924,bilateral perisylvian polymicrogyria,C3810405,,615752,MONDO:0014333,"polymicrogyria, bilateral perisylvian, autosomal recessive",
+BMGC_DS15268,BMG_DS057152,,,,,,,,,C3810406,,615761,MONDO:0014336,intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency,
+BMGC_DS15269,BMG_DS057153,,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5",,,,,DOID:0090135,complex cortical dysplasia with other brain malformations 5,C3810407,,615763;615101,MONDO:0014337,complex cortical dysplasia with other brain malformations 5,
+BMGC_DS15270,BMG_DS057154,1268466004,Low frequency sensorineural hearing loss,,,,,,,C3810445,,,,,Low frequency sensorineural hearing loss | Low frequency sensorineural hearing loss (disorder) | Low tone sensorineural hearing loss
+BMGC_DS15271,BMG_DS057168,,Mycoplasma pneumoniae Infection,"Pneumonia, Mycoplasma",,,,DOID:13276,Mycoplasma pneumoniae pneumonia,C3824874,D011019,,,,
+BMGC_DS15272,BMG_DS057182,700220003;194201001;39149004,Acute bacterial otitis externa,,,,,DOID:10518,beach ear,C3831782,,,,,Acute bacterial otitis externa (disorder) | Acute bacterial otitis externa | Tank ear | Beach ear | Acute swimmer's ear | Acute swimmer's ear (disorder) | Acute bacterial otitis externa | Acute bacterial inflammation of external ear | Acute diffuse otitis externa | Acute bacterial inflammation of external ear | Acute swimmers' ear | Beach ear | Tank ear | Acute diffuse otitis externa | Acute bacterial otitis externa | Acute swimmer's ear | Acute bacterial inflammation of external ear (disorder)
+BMGC_DS15273,BMG_DS057187,,"MECKEL SYNDROME, TYPE 8",,,,,,,C3836857,,613885;613846,MONDO:0013482,"Meckel syndrome, type 8",
+BMGC_DS15274,BMG_DS057188,,"HYPERTENSION, SALT-SENSITIVE ESSENTIAL, SUSCEPTIBILITY TO",,,,,,,C3837651,,605325;102680,,,
+BMGC_DS15275,BMG_DS057190,,"Diabetes Mellitus, Ketosis-Prone","Diabetes Mellitus, Type 1",,,,,,C3837958,D003922,612227,MONDO:0100180,"diabetes mellitus, ketosis-prone",
+BMGC_DS15276,BMG_DS057191,,,,,,,,,C3838076,,,MONDO:0100167,"pulmonary disease, chronic obstructive, susceptibility to",
+BMGC_DS15277,BMG_DS057201,703232003,Familial hyperaldosteronism type 1,,,,,DOID:14080,glucocorticoid-remediable aldosteronism,C3838731,,103900,MONDO:0007080,glucocorticoid-remediable aldosteronism,Familial hyperaldosteronism type 1 | Familial hyperaldosteronism type 1 (disorder) | Glucocorticoid-sensitive hypertension | Glucocorticoid-suppressible hyperaldosteronism | Glucocorticoid-remediable aldosteronism | Familial hyperaldosteronism type I | Dexamethasone-sensitive hypertension | GRA - glucocorticoid-remediable aldosteronism
+BMGC_DS15278,BMG_DS057208,703234002,Familial hyperaldosteronism type 3,,,,,,,C3838758,,613677,MONDO:0013359,familial hyperaldosteronism type III,Familial hyperaldosteronism type 3 (disorder) | Familial hyperaldosteronism type 3
+BMGC_DS15279,BMG_DS057238,700112007,Bartter syndrome type 4,,,,,,,C3838860,,,MONDO:0019524,Bartter syndrome type 4,Bartter syndrome type 4 | Bartter syndrome type 4 (disorder) | Bartter's syndrome type 4
+BMGC_DS15280,BMG_DS057244,,,,,,,,,C3838883,,,MONDO:0019325,phakomatosis cesioflammea,
+BMGC_DS15281,BMG_DS057317,703266007,Cerebrofacial arteriovenous metameric syndrome,,,,,,,C3839265,,,MONDO:0015405,cerebrofacial arteriovenous metameric syndrome,Cerebrofacial arteriovenous metameric syndrome | Cerebrofacial arteriovenous metameric syndrome (disorder)
+BMGC_DS15282,BMG_DS057323,,,,,,,,,C3839296,,,MONDO:0019326,phakomatosis cesiomarmorata,
+BMGC_DS15283,BMG_DS057422,,,,,,,DOID:7839,infiltrating nipple syringomatous adenoma,C3839745,,,MONDO:0004376,infiltrating nipple syringomatous adenoma,
+BMGC_DS15284,BMG_DS057442,,,,,,,,,C3839822,,,MONDO:0100216,DICER1-related tumor predisposition,
+BMGC_DS15285,BMG_DS057455,703226008,Familial cerebral saccular aneurysm,,,,,,,C3839866,,,MONDO:0016483,intracranial berry aneurysm,Familial cerebral saccular aneurysm (disorder) | Familial cerebral saccular aneurysm | Familial intracranial saccular aneurysm | Familial berry aneurysm
+BMGC_DS15286,BMG_DS057468,,,,,,,,,C3839921,,,MONDO:0015408,diffuse lymphatic malformation,
+BMGC_DS15287,BMG_DS057553,,,,,,,DOID:4894,rete ovarii adenocarcinoma,C3840223,,,MONDO:0003191,rete ovarii adenocarcinoma,
+BMGC_DS15288,BMG_DS057557,,,,,,,,,C3840252,,,MONDO:0975754,pseudomyogenic hemangioendothelioma,
+BMGC_DS15289,BMG_DS057562,79592006,Beta plus thalassemia,,,,,,,C3841475,,,,,Beta plus thalassemia | Beta plus thalassaemia | Beta plus thalassemia (disorder) | beta plus thalassaemia | beta plus thalassemia
+BMGC_DS15290,BMG_DS057566,,Acute Mesenteric Arterial Embolus,Mesenteric Ischemia,,,,,,C3852984,D065666,,,,
+BMGC_DS15291,BMG_DS057567,,Occlusive Mesenteric Arterial Ischemia,Mesenteric Ischemia,,,,,,C3852985,D065666,,,,
+BMGC_DS15292,BMG_DS057568,,Nonocclusive Mesenteric Ischemia,Mesenteric Ischemia,,,,,,C3852986,D065666,,,,
+BMGC_DS15293,BMG_DS057569,,Acute Mesenteric Arterial Thrombosis,Mesenteric Ischemia,,,,,,C3852987,D065666,,,,
+BMGC_DS15294,BMG_DS057571,,Severe Congenital Microcephaly,Microcephaly,,,,,,C3853041,D008831,,,,
+BMGC_DS15295,BMG_DS057578,,Erosive Duodenitis,Duodenitis,,,,,,C3853541,D004382,,,,
+BMGC_DS15296,BMG_DS057580,,Neonatal Alloimmune Thrombocytopenia,"Thrombocytopenia, Neonatal Alloimmune",,,,,,C3853779,D054098,,,,
+BMGC_DS15297,BMG_DS057584,705149003,Lipodystrophy due to Human immunodeficiency virus infection and antiretroviral therapy,,,,,,,C3854116,,,,,Lipodystrophy due to HIV and antiretroviral therapy | Lipodystrophy due to Human immunodeficiency virus infection and antiretroviral therapy | Lipodystrophy associated with Human immunodeficiency virus infection | Lipodystrophy due to Human immunodeficiency virus infection and antiretroviral therapy (disorder)
+BMGC_DS15298,BMG_DS057586,,,,,,,DOID:0111530,linear nevus sebaceous syndrome,C3854181,,,,,
+BMGC_DS15299,BMG_DS057595,763803004,Morvan syndrome,,,,,,,C3854373,,,MONDO:0008718,Morvan syndrome,"Morvan syndrome (disorder) | Morvan syndrome | Limbic encephalitis, neuromyotonia, hyperhidrosis, polyneuropathy syndrome | Morvan fibrillary chorea"
+BMGC_DS15300,BMG_DS057597,,Hyperferritinemia,Hyperferritinemia,,,,,,C3854388,D000085583,620729;MTHU070680,MONDO:0958237,isolated hyperferritinemia,
+BMGC_DS15301,BMG_DS057607,,,,,,,,,C3854603,,,MONDO:0019415,fetal and neonatal alloimmune thrombocytopenia,
+BMGC_DS15302,BMG_DS057716,708126004,Recurrent candidiasis of vagina,,,,,,,C3872606,,,,,Recurrent candidiasis of vagina | Recurrent candidiasis of vagina (disorder)
+BMGC_DS15303,BMG_DS057727,708030004,Pulmonary emphysema co-occurrent with fibrosis of lung,,,,,,,C3872815,,,MONDO:0017591,combined pulmonary fibrosis-emphysema syndrome,CPFE - combined pulmonary fibrosis and emphysema | Combined pulmonary fibrosis and emphysema syndrome | Pulmonary emphysema co-occurrent with fibrosis of lung (disorder) | Pulmonary emphysema co-occurrent with fibrosis of lung
+BMGC_DS15304,BMG_DS057831,,Dermatophagoides pteronyssinus Allergy,Dust Mite Allergy,,,,,,C3873561,D000092542,,,,
+BMGC_DS15305,BMG_DS057850,,,,,,,,,C3874315,,113600,MONDO:0007233,second branchial cleft anomaly,
+BMGC_DS15306,BMG_DS057861,136801000119102,Therapeutic opioid induced constipation,,,,,,,C3874358,,,,,Therapeutic opioid induced constipation (disorder) | Therapeutic opioid induced constipation
+BMGC_DS15307,BMG_DS057873,29731000119103,Intestinal hemorrhage due to angiodysplasia of intestine,,,,,,,C3874401,,,,,Intestinal haemorrhage due to angiodysplasia of intestine | Intestinal hemorrhage due to angiodysplasia of intestine | Intestinal hemorrhage due to angiodysplasia of intestine (disorder)
+BMGC_DS15308,BMG_DS057934,15771000119109,Familial hyperalphalipoproteinemia,,,,,,,C3875011,,143470,MONDO:0007744,cholesterol-ester transfer protein deficiency,Familial hyperalphalipoproteinemia | Familial hyperalphalipoproteinemia (disorder) | Familial hyperalphalipoproteinaemia
+BMGC_DS15309,BMG_DS057996,109041000119107,Complex dyslipidemia,,,,,,,C3875286,,,,,Complex dyslipidemia | Complex dyslipidemia (disorder)
+BMGC_DS15310,BMG_DS058001,703938007,Inflammatory dermatosis,,,,,,,C3875321,,,MONDO:0002406,dermatitis,Inflammatory dermatosis (disorder) | Inflammatory dermatosis | Dermatitis
+BMGC_DS15311,BMG_DS058022,,Dermatophagoides farinae Allergy,Dust Mite Allergy,,,,,,C3875472,D000092542,,,,
+BMGC_DS15312,BMG_DS058038,,"Neutrophil Chemotactic Response, Abnormal",,,,,,,C3882647,C563515,,,,
+BMGC_DS15313,BMG_DS058041,,,,,,,,,C3887485,,157300,MONDO:0008000,"migraine with or without aura, susceptibility to, 1",
+BMGC_DS15314,BMG_DS058042,715704001,Postaxial polydactyly type A,,,,,,,C3887487,,,MONDO:0019673,postaxial polydactyly type A,Postaxial polydactyly type A (disorder) | Postaxial polydactyly type A
+BMGC_DS15315,BMG_DS058045,,"ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE",,,,,DOID:0111665,ectodermal dysplasia 10B,C3887494,,224900;604095,MONDO:0009147,"ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive",
+BMGC_DS15316,BMG_DS058047,,,,,,,,,C3887497,,210400,MONDO:0008866,"bifid nose, autosomal recessive",
+BMGC_DS15317,BMG_DS058048,722223000,Renal cyst,,,,,,,C3887499,,MTHU019013,MONDO:0002473,cystic kidney disease,Cyst of kidney (disorder) | Cyst of kidney | Renal cyst
+BMGC_DS15318,BMG_DS058049,,,,,,,,,C3887501,,608709,MONDO:0100476,"lipodystrophy, partial, acquired, susceptibility to",
+BMGC_DS15319,BMG_DS058050,44548000,Hyperkinesia,Hyperkinesis,,,,,,C3887506,D006948,MTHU026101,,,Hyperkinesia | Hyperkinesis | Increased purposeful goal-directed activity | Hyperactive behaviour | Hyperactive behavior | HA - Hyperactivity | Hyperactive behavior (finding)
+BMGC_DS15320,BMG_DS058052,237997005,Very long chain acyl-CoA dehydrogenase deficiency,,,,,,,C3887523,,201475,MONDO:0008723,very long chain acyl-CoA dehydrogenase deficiency,Very long chain acyl-CoA dehydrogenase deficiency | VLCAD - Very long chain acyl-CoA dehydrogenase deficiency | Very long chain acyl-coenzyme A dehydrogenase deficiency (disorder) | Very long chain acyl-coenzyme A dehydrogenase deficiency
+BMGC_DS15321,BMG_DS058053,,"Keratosis Follicularis Spinulosa Decalvans, X-Linked",,,,,,,C3887525,C536159,308800,MONDO:0010637,"keratosis follicularis spinulosa decalvans, X-linked",
+BMGC_DS15322,BMG_DS058054,,,,,,,,,C3887526,,140600,MONDO:0007704,osteoarthritis susceptibility 2,
+BMGC_DS15323,BMG_DS058055,388840007,Keratoglobus,Keratoconus,,,,,,C3887531,D007640,MTHU012982,,,Keratoglobus (disorder) | Keratoglobus | Cornea globular
+BMGC_DS15324,BMG_DS058058,,Hemophagocytic Syndrome,"Lymphohistiocytosis, Hemophagocytic",,,,,,C3887558,D051359,,MONDO:0015540,hemophagocytic syndrome,
+BMGC_DS15325,BMG_DS058062,,"HYDROCEPHALUS, CONGENITAL, 1",,,,,,,C3887608,,236600;611204,MONDO:0009360,"hydrocephalus, nonsyndromic, autosomal recessive 1",
+BMGC_DS15326,BMG_DS058063,,"Dandy-Walker Syndrome, Familial",Dandy-Walker Syndrome,,,,,,C3887633,D003616,,,,
+BMGC_DS15327,BMG_DS058065,84568007,Autoimmune gastritis,,,,,,,C3887639,,,MONDO:0031014,autoimmune gastritis,Atrophic gastritis | Chronic atrophic gastritis | Gastric atrophy | AG - Atrophic gastritis | Autoimmune gastritis | CAG - Chronic atrophic gastritis | Atrophic gastritis (disorder)
+BMGC_DS15328,BMG_DS058067,,Job Syndrome,Job Syndrome,,,,,,C3887645,D007589,,MONDO:0018037,hyper-IgE syndrome,
+BMGC_DS15329,BMG_DS058068,,Adult Rickets,Osteomalacia,,,,,,C3887650,D010018,,,,
+BMGC_DS15330,BMG_DS058070,,"POLYARTERITIS NODOSA, CHILDHOOD-ONSET",,,,,,,C3887654,,615688,MONDO:0014306,vasculitis due to ADA2 deficiency,
+BMGC_DS15331,BMG_DS058071,,"PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT",,,,,DOID:0081268,pulmonary venoocclusive disease 1,C3887658,,265450,MONDO:0020713,pulmonary venoocclusive disease 1,
+BMGC_DS15332,BMG_DS058074,88264003,Infection by larvae of Trichinella spiralis,,,,,,,C3887668,,,MONDO:0042458,Trichinella spiralis infectious disease,Infection by larvae of Trichinella spiralis | Trichinosis caused by Trichinella spiralis | Trichinellosis caused by Trichinella spiralis | Trichinelliasis caused by Trichinella spiralis | Trichiniasis caused by Trichinella spiralis | Infection caused by larvae of Trichinella spiralis (disorder) | Infection caused by larvae of Trichinella spiralis
+BMGC_DS15333,BMG_DS058079,,,,,,,,,C3887709,,,MONDO:0002135,optic nerve disorder,
+BMGC_DS15334,BMG_DS058080,,WILMS TUMOR 2,,,,,,,C3887743,,616186;605982;194071;194071,MONDO:0008680,Wilms tumor 2,
+BMGC_DS15335,BMG_DS058082,,,,,,,,,C3887876,,165720,MONDO:0008143,osteoarthritis susceptibility 1,
+BMGC_DS15336,BMG_DS058085,,Aortic Valve Disease 1,Bicuspid Aortic Valve Disease,,,,DOID:0080332,bicuspid aortic valve disease,C3887892,D000082882,109730,MONDO:0024523,aortic valve disease 1,
+BMGC_DS15337,BMG_DS058087,711167005;80960004,Enteritis due to Yersinia enterocolitica,,1A05,Intestinal infections due to Yersinia enterocolitica,A04.6,,,C3887894,,,,,Enteritis caused by Yersinia enterocolitica | Enteritis caused by Yersinia enterocolitica (disorder) | Infection by Yersinia enterocolitica | Infection caused by Yersinia enterocolitica | Infection caused by Yersinia enterocolitica (disorder)
+BMGC_DS15338,BMG_DS058091,,"CATARACT 32, MULTIPLE TYPES",,,,,,,C3887926,,115650,MONDO:0007278,cataract 32 multiple types,
+BMGC_DS15339,BMG_DS058092,,"DEAFNESS, AUTOSOMAL DOMINANT 27",,,,,,,C3887929,,600571;612431,MONDO:0012902,autosomal dominant nonsyndromic hearing loss 27,
+BMGC_DS15340,BMG_DS058093,,"DEAFNESS, AUTOSOMAL DOMINANT 33",,,,,,,C3887930,,614211,MONDO:0013632,autosomal dominant nonsyndromic hearing loss 33,
+BMGC_DS15341,BMG_DS058094,,"MYOCLONIC EPILEPSY, JUVENILE, 2",,,,,DOID:0111321,idiopathic generalized epilepsy 7,C3887932,,604827,MONDO:0800330,"myoclonic epilepsy, juvenile, 2",
+BMGC_DS15342,BMG_DS058095,,"CONE DYSTROPHY 5, X-LINKED",,,,,DOID:0050679,blue cone monochromacy,C3887937,,300821;303700,MONDO:0800319,"cone dystrophy 5, X-linked",
+BMGC_DS15343,BMG_DS058096,77479002,Deuteranomaly,,,,H53.53,,,C3887938,,,,,Deutan defect | Deuteranomaly | Deuteranopia | Deutan defect (disorder)
+BMGC_DS15344,BMG_DS058097,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 41",,,,,DOID:0112058,non-syndromic X-linked intellectual disability 41,C3887939,,300849;300104,MONDO:0010451,"intellectual disability, X-linked 41",
+BMGC_DS15345,BMG_DS058098,,"GLAUCOMA 1, OPEN ANGLE, B",,,,,,,C3887942,,606689,,,
+BMGC_DS15346,BMG_DS058100,,POLYCYSTIC KIDNEY DISEASE 3 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE,,,,,DOID:0110860,polycystic kidney disease 3,C3887964,,600666;104160,MONDO:0010916,polycystic kidney disease 3 with or without polycystic liver disease,
+BMGC_DS15347,BMG_DS058101,,"RETINAL DYSPLASIA, PRIMARY",,,,,,,C3887971,,312550,,,
+BMGC_DS15348,BMG_DS058102,51445007,Protanomaly,,,,H53.54,,,C3887980,,,,,Protan defect | Protanomaly | Protanopia | Protan defect (disorder)
+BMGC_DS15349,BMG_DS058104,,RETINITIS PIGMENTOSA 24,,,,,,,C3887982,,300155,MONDO:0010259,retinitis pigmentosa 24,
+BMGC_DS15350,BMG_DS058105,,SPINOCEREBELLAR ATAXIA 9,,,,,DOID:0111747,cerebellar ataxia type 9,C3887996,,612876,MONDO:0013029,cerebellar ataxia type 9,
+BMGC_DS15351,BMG_DS058106,,HERMANSKY-PUDLAK SYNDROME 3,,,,,DOID:0060541,Hermansky-Pudlak syndrome 3,C3888001,,614072;606118,MONDO:0013555,Hermansky-Pudlak syndrome 3,
+BMGC_DS15352,BMG_DS058107,,"PULMONARY HYPERTENSION, PRIMARY, 2",,,,,,,C3888002,,615342;603295,MONDO:0014134,"pulmonary hypertension, primary, 2",
+BMGC_DS15353,BMG_DS058108,,HERMANSKY-PUDLAK SYNDROME 5,,,,,DOID:0060543,Hermansky-Pudlak syndrome 5,C3888004,,614074;607521,MONDO:0013557,Hermansky-Pudlak syndrome 5,
+BMGC_DS15354,BMG_DS058109,,HERMANSKY-PUDLAK SYNDROME 6,,,,,DOID:0060544,Hermansky-Pudlak syndrome 6,C3888007,,614075;607522,MONDO:0013558,Hermansky-Pudlak syndrome 6,
+BMGC_DS15355,BMG_DS058110,,"MACULAR DYSTROPHY, RETINAL, 3",,,,,DOID:0070440,retinal macular dystrophy 3,C3888009,,608850,MONDO:0012139,"macular dystrophy, retinal, 3",
+BMGC_DS15356,BMG_DS058112,,Congenital Hyperinsulinism,Congenital Hyperinsulinism,,,,,,C3888018,D044903,,MONDO:0017182,familial hyperinsulinism,
+BMGC_DS15357,BMG_DS058113,,Cacosmia,Olfaction Disorders,,,,,,C3888024,D000857,,,,
+BMGC_DS15358,BMG_DS058114,,HERMANSKY-PUDLAK SYNDROME 8,,,,,DOID:0060546,Hermansky-Pudlak syndrome 8,C3888026,,609762;614077,MONDO:0013560,Hermansky-Pudlak syndrome 8,
+BMGC_DS15359,BMG_DS058116,,"DEAFNESS, AUTOSOMAL DOMINANT 54",,,,,,,C3888029,,615649,MONDO:0014291,autosomal dominant nonsyndromic hearing loss 54,
+BMGC_DS15360,BMG_DS058117,,"DEAFNESS, AUTOSOMAL RECESSIVE 45",,,,,,,C3888030,,612433,MONDO:0012903,autosomal recessive nonsyndromic hearing loss 45,
+BMGC_DS15361,BMG_DS058118,,SPINOCEREBELLAR ATAXIA 35,,,,,DOID:0050982,spinocerebellar ataxia type 35,C3888031,,613900;613908,MONDO:0013485,spinocerebellar ataxia type 35,
+BMGC_DS15362,BMG_DS058120,,"ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT",,,,,DOID:0111663,ectodermal dysplasia 10A,C3888065,,129490,MONDO:0007509,"ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant",
+BMGC_DS15363,BMG_DS058121,,"DEAFNESS, Y-LINKED 1",,,,,DOID:0111759,Y-linked deafness 1,C3888076,,400043,MONDO:0010764,"hearing loss, Y-linked 1",
+BMGC_DS15364,BMG_DS058122,,"Charcot-Marie-Tooth disease, Type 2I",,,,,DOID:0110158,Charcot-Marie-Tooth disease type 2I,C3888087,C535416,607677,MONDO:0011889,Charcot-Marie-Tooth disease type 2I,
+BMGC_DS15365,BMG_DS058123,,SMITH-MCCORT DYSPLASIA 1,,,,,DOID:0081270,Smith-McCort dysplasia 1,C3888088,,607461;607326,MONDO:0011814,Smith-McCort dysplasia 1,
+BMGC_DS15366,BMG_DS058124,,"Deafness, X-Linked 3",,,,,,,C3888089,C564727,300030,MONDO:0010228,"hearing loss, X-linked 3",
+BMGC_DS15367,BMG_DS058125,,Early onset torsion dystonia,,,,,,,C3888090,C538005,,,,
+BMGC_DS15368,BMG_DS058126,,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2",,,,,,,C3888093,,242100;603741,MONDO:0009439,autosomal recessive congenital ichthyosis 2,
+BMGC_DS15369,BMG_DS058128,711162004,Autosomal dominant vitreoretinochoroidopathy,,,,,DOID:0111569,autosomal dominant vitreoretinochoroidopathy,C3888099,,193220,MONDO:0008662,autosomal dominant vitreoretinochoroidopathy,"Autosomal dominant vitreoretinochoroidopathy (disorder) | Autosomal dominant vitreoretinochoroidopathy | Vitreoretinochoroidopathy with microcornea, glaucoma and cataract | Autosomal dominant vitreoretinochoroidopathy with nanophthalmos"
+BMGC_DS15370,BMG_DS058129,,Frontotemporal Dementia With Motor Neuron Disease,,,,,,,C3888102,C566288,,MONDO:0017161,frontotemporal dementia with motor neuron disease,
+BMGC_DS15371,BMG_DS058130,818952002,Glomerulopathy with fibronectin deposits,,,,,,,C3888104,C536826,,MONDO:0007671,fibronectin glomerulopathy,Fibronectin glomerulopathy | Glomerulopathy with fibronectin deposits | Fibronectin glomerulopathy (disorder)
+BMGC_DS15372,BMG_DS058131,,,,,,,,,C3888106,,126200,MONDO:0021571,"multiple sclerosis, susceptibility to 1",
+BMGC_DS15373,BMG_DS058133,,"DEAFNESS, AUTOSOMAL DOMINANT 50",,,,,,,C3888123,,611606;613074,MONDO:0013114,autosomal dominant nonsyndromic hearing loss 50,
+BMGC_DS15374,BMG_DS058134,,"CATARACT 17, MULTIPLE TYPES",,,,,,,C3888124,,611544,MONDO:0012688,cataract 17 multiple types,
+BMGC_DS15375,BMG_DS058135,,"BESTROPHINOPATHY, AUTOSOMAL RECESSIVE",,,,,,,C3888198,,607854;611809,MONDO:0012733,autosomal recessive bestrophinopathy,
+BMGC_DS15376,BMG_DS058136,,APOLIPOPROTEIN A-II DEFICIENCY,,,,,,,C3888202,,107670,,,
+BMGC_DS15377,BMG_DS058137,,ACTN3 DEFICIENCY,,,,,,,C3888204,,617749;102574,,,
+BMGC_DS15378,BMG_DS058138,,"SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT",,,,,,,C3888208,,613364,MONDO:0013239,hereditary spastic paraplegia 41,
+BMGC_DS15379,BMG_DS058139,,"SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE",,,,,,,C3888209,,613162,MONDO:0013165,hereditary spastic paraplegia 45,
+BMGC_DS15380,BMG_DS058140,,"DEAFNESS, AUTOSOMAL DOMINANT 58",,,,,,,C3888210,,615654,MONDO:0014293,autosomal dominant nonsyndromic hearing loss 58,
+BMGC_DS15381,BMG_DS058141,,"MYOPIA 17, AUTOSOMAL DOMINANT",,,,,,,C3888211,,608367,MONDO:0012021,"myopia 17, autosomal dominant",
+BMGC_DS15382,BMG_DS058142,,SECKEL SYNDROME 4,,,,,DOID:0070010,Seckel syndrome 4,C3888212,,613676;609279,MONDO:0013358,Seckel syndrome 4,
+BMGC_DS15383,BMG_DS058143,,,,,,,,,C3888239,,142623,MONDO:0007723,"Hirschsprung disease, susceptibility to, 1",
+BMGC_DS15384,BMG_DS058144,,AICARDI-GOUTIERES SYNDROME 7,,,,,,,C3888244,,606951;615846,MONDO:0014367,Aicardi-Goutieres syndrome 7,
+BMGC_DS15385,BMG_DS058145,,,,,,,,,C3888271,,615575,MONDO:0014259,"neuronopathy, distal hereditary motor, type 2D",
+BMGC_DS15386,BMG_DS058146,,"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT",,,,,DOID:0070028,APP-related cerebral amyloid angiopathy,C3888307,,605714;104760,MONDO:0017948,ABetaA21G amyloidosis,
+BMGC_DS15387,BMG_DS058147,,"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT",,,,,DOID:0070028,APP-related cerebral amyloid angiopathy,C3888308,,605714;104760,MONDO:0017947,"ABeta amyloidosis, Italian type",
+BMGC_DS15388,BMG_DS058148,,"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT",,,,,DOID:0070028,APP-related cerebral amyloid angiopathy,C3888309,,104760;605714,MONDO:0017946,"ABeta amyloidosis, Iowa type",
+BMGC_DS15389,BMG_DS058149,,"DEAFNESS, AUTOSOMAL RECESSIVE 83",,,,,,,C3888310,,613685,MONDO:0013365,autosomal recessive nonsyndromic hearing loss 83,
+BMGC_DS15390,BMG_DS058151,,"Myopathy, familial idiopathic inflammatory",,,,,,,C3888318,C000598744,160750,MONDO:0600024,familial idiopathic inflammatory myopathy,
+BMGC_DS15391,BMG_DS058152,,"DEAFNESS, AUTOSOMAL RECESSIVE 96",,,,,,,C3888337,,614414,MONDO:0013738,autosomal recessive nonsyndromic hearing loss 96,
+BMGC_DS15392,BMG_DS058153,,"GLAUCOMA 1, OPEN ANGLE, P",,,,,,,C3888338,,177700,MONDO:0008328,"glaucoma 1, open angle, P",
+BMGC_DS15393,BMG_DS058154,,OTOSCLEROSIS 10,,,,,DOID:0060927,otosclerosis 10,C3888339,,615589,MONDO:0014264,otosclerosis 10,
+BMGC_DS15394,BMG_DS058155,,"DEAFNESS, AUTOSOMAL RECESSIVE 93",,,,,,,C3888355,,614899;607314,MONDO:0013963,autosomal recessive nonsyndromic hearing loss 93,
+BMGC_DS15395,BMG_DS058156,,,,,,,,,C3888385,,614872,MONDO:0013938,peroxisome biogenesis disorder 7A (Zellweger),
+BMGC_DS15396,BMG_DS058158,,,,,,,,,C3888401,,615312,MONDO:0014127,oculocutaneous albinism type 5,
+BMGC_DS15397,BMG_DS058159,,"CATARACT 5, MULTIPLE TYPES",,,,,,,C3888417,,116800,,,
+BMGC_DS15398,BMG_DS058160,,,,,,,,,C3888523,,,MONDO:0031012,autoimmune uveitis,
+BMGC_DS15399,BMG_DS058161,,,,,,,,,C3888631,,,MONDO:0015967,monogenic diabetes,
+BMGC_DS15400,BMG_DS058162,,Hemorrhagic Necrotic Pancreatitis,"Pancreatitis, Acute Necrotizing",,,,DOID:0080998,acute necrotizing pancreatitis,C3888668,D019283,,,,
+BMGC_DS15401,BMG_DS058163,,Hyperosmolar Hyperglycemic State,Hyperglycemic Hyperosmolar Nonketotic Coma,,,,,,C3888846,D006944,,,,
+BMGC_DS15402,BMG_DS058166,722302009,"Glycogen storage disease due to acid maltase deficiency, infantile onset",,,,,,,C3888924,,,MONDO:0017694,"glycogen storage disease due to acid maltase deficiency, infantile onset","Glycogen storage disease due to acid maltase deficiency, infantile onset | Glycogenosis due to acid maltase deficiency, infantile onset | Glycogenosis type II, infantile onset | Pompe disease, infantile onset | Glycogen storage disease type II infantile onset | Glycogen storage disease due to acid maltase deficiency, infantile onset (disorder)"
+BMGC_DS15403,BMG_DS058167,,Cryptococcus gattii Infection,Cryptococcosis,,,,,,C3888929,D003453,,,,
+BMGC_DS15404,BMG_DS058169,,Non-Radiographic Axial Spondyloarthritis,Non-Radiographic Axial Spondyloarthritis,,,,,,C3889038,D000089202,,,,
+BMGC_DS15405,BMG_DS058170,,BARDET-BIEDL SYNDROME 16,,,,,,,C3889474,,615993;613524,MONDO:0014444,Bardet-Biedl syndrome 16,
+BMGC_DS15406,BMG_DS058171,,BARDET-BIEDL SYNDROME 19,,,,,,,C3889475,,615870;615996,MONDO:0014447,Bardet-Biedl syndrome 19,
+BMGC_DS15407,BMG_DS058172,,SPINOCEREBELLAR ATAXIA 37,,,,,DOID:0050984,spinocerebellar ataxia type 37,C3889636,,603448;615945,MONDO:0014410,spinocerebellar ataxia type 37,
+BMGC_DS15408,BMG_DS058174,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 100",,,,,DOID:0112040,non-syndromic X-linked intellectual disability 100,C3890167,,300521;300923,MONDO:0010488,"intellectual disability, X-linked 100",
+BMGC_DS15409,BMG_DS058175,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 101",,,,,DOID:0112048,non-syndromic X-linked intellectual disability 101,C3890168,,300204;300928,MONDO:0010489,"intellectual disability, X-linked 101",
+BMGC_DS15410,BMG_DS058176,,,,,,,,,C3890205,,,MONDO:0019432,rheumatoid factor-negative juvenile idiopathic arthritis,
+BMGC_DS15411,BMG_DS058178,,NEPHRONOPHTHISIS 18,,,,,DOID:0111125,nephronophthisis 18,C3890591,,615847;615862,MONDO:0014374,nephronophthisis 18,
+BMGC_DS15412,BMG_DS058180,,,,,,,,,C3890737,,,MONDO:0019751,autoinflammatory syndrome,
+BMGC_DS15413,BMG_DS058182,,,,,,,,,C3891301,,616806,MONDO:0014779,Wilms tumor 6,
+BMGC_DS15414,BMG_DS058183,,,,,,,,,C3891448,,182940,MONDO:0020705,"neural tube defects, susceptibility to",
+BMGC_DS15415,BMG_DS058184,,SECKEL SYNDROME 8,,,,,DOID:0070009,Seckel syndrome 8,C3891452,,601810;615807,MONDO:0014350,Seckel syndrome 8,
+BMGC_DS15416,BMG_DS058185,,CHROMOSOME Xq26.3 DUPLICATION SYNDROME,,,,,,,C3891556,,300942,MONDO:0010491,X-linked acrogigantism due to Xq26 microduplication,
+BMGC_DS15417,BMG_DS058187,,"Arthritis, Suppurative","Arthritis, Infectious",,,,,,C3891815,D001170,,,,
+BMGC_DS15418,BMG_DS058188,,PANCREATIC AGENESIS 1,,,,,DOID:0061003,pancreatic agenesis 1,C3891828,,260370;600733,MONDO:0024547,pancreatic agenesis 1,
+BMGC_DS15419,BMG_DS058189,,BARDET-BIEDL SYNDROME 5,,,,,,,C3892039,,603650;615983,MONDO:0014434,Bardet-Biedl syndrome 5,
+BMGC_DS15420,BMG_DS058190,,"DEAFNESS, AUTOSOMAL DOMINANT 65",,,,,,,C3892048,,616044;613577,MONDO:0014470,autosomal dominant nonsyndromic hearing loss 65,
+BMGC_DS15421,BMG_DS058191,,"DEAFNESS, AUTOSOMAL RECESSIVE 101",,,,,,,C3892049,,615837;615762,MONDO:0014363,autosomal recessive nonsyndromic hearing loss 101,
+BMGC_DS15422,BMG_DS058192,,"DEAFNESS, AUTOSOMAL RECESSIVE 102",,,,,,,C3892050,,615974;600206,MONDO:0014428,autosomal recessive nonsyndromic hearing loss 102,
+BMGC_DS15423,BMG_DS058193,,,,,,,,,C3896578,,,MONDO:0018604,familial colorectal cancer type X,
+BMGC_DS15424,BMG_DS058196,,,,,,,,,C3897042,,,MONDO:0015557,Smouldering systemic mastocytosis,
+BMGC_DS15425,BMG_DS058205,,DISABLING PANSCLEROTIC MORPHEA OF CHILDHOOD,,,,,,,C3898649,,620443;600558,MONDO:0957497,disabling pansclerotic morphea of childhood,
+BMGC_DS15426,BMG_DS058215,,,,,,,,,C3899764,,,MONDO:0956989,CIC-rearranged sarcoma,
+BMGC_DS15427,BMG_DS058219,,,,,,,,,C3900122,,615961,MONDO:0014420,short stature due to primary acid-labile subunit deficiency,
+BMGC_DS15428,BMG_DS058220,,"AMELOGENESIS IMPERFECTA, TYPE IA",,,,,,,C4011403,,150310;104530,MONDO:0007094,amelogenesis imperfecta type 1A,
+BMGC_DS15429,BMG_DS058221,,CATARACT 42,,,,,,,C4011454,,600836;115900,MONDO:0007283,cataract 42,
+BMGC_DS15430,BMG_DS058222,,"MYOPATHY, DISTAL, INFANTILE-ONSET",,,,,DOID:0070196,infantile-onset distal myopathy,C4011725,,160300,MONDO:0008049,"myopathy, distal, infantile-onset",
+BMGC_DS15431,BMG_DS058223,,"MYOPATHY, TUBULAR AGGREGATE, 1",,,,,DOID:0080089,tubular aggregate myopathy 1,C4011726,,160565;605921,MONDO:0024531,"myopathy, tubular aggregate, 1",
+BMGC_DS15432,BMG_DS058224,716994006,Behavioral variant of frontotemporal dementia,,,,,,,C4011788,,,MONDO:0017160,behavioral variant of frontotemporal dementia,Behavioral variant of frontotemporal dementia (disorder) | Behavioral variant of frontotemporal dementia | Behavioural variant of frontotemporal dementia
+BMGC_DS15433,BMG_DS058225,,WHITE SPONGE NEVUS 1,,,,,DOID:0081287,white sponge nevus 1,C4011926,,193900;123940,MONDO:0008676,white sponge nevus 1,
+BMGC_DS15434,BMG_DS058227,,IMMUNODEFICIENCY 27A,,,,,,,C4011949,,107470;209950,MONDO:0008856,immunodeficiency 27A,
+BMGC_DS15435,BMG_DS058228,,"COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE",,,,,,,C4011974,,216820;602219,MONDO:0009002,"coloboma, ocular, autosomal recessive",
+BMGC_DS15436,BMG_DS058230,,HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 1,,,,,,,C4012050,,612753;235510,MONDO:0009337,Hennekam lymphangiectasia-lymphedema syndrome 1,
+BMGC_DS15437,BMG_DS058231,,"NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID",,,,,,,C4012054,,243000;603415,MONDO:0800304,"neuropathy, hereditary sensory and autonomic, type IId",
+BMGC_DS15438,BMG_DS058234,,DESBUQUOIS DYSPLASIA 1,,,,,,,C4012146,,613165;251450,MONDO:0009629,Desbuquois dysplasia 1,
+BMGC_DS15439,BMG_DS058235,,Neonatal pulmonary hypertension,,,,,,,C4012212,,MTHU045623,,,
+BMGC_DS15440,BMG_DS058238,,"TETRAAMELIA SYNDROME, AUTOSOMAL RECESSIVE",,,,,DOID:0112192,tetraamelia syndrome 1,C4012268,,273395,MONDO:0060764,tetraamelia syndrome 1,
+BMGC_DS15441,BMG_DS058240,733115009,Congenital disorder of glycosylation type 1y,,,,,,,C4012395,,300934,MONDO:0010490,SSR4-congenital disorder of glycosylation,Signal sequence receptor subunit 4 congenital disorder of glycosylation | Congenital disorder of glycosylation type Iy | SSR4-CDG - signal sequence receptor subunit 4 congenital disorder of glycosylation | Congenital disorder of glycosylation type 1y | Carbohydrate deficient glycoprotein syndrome type Iy | Congenital disorder of glycosylation type 1y (disorder)
+BMGC_DS15442,BMG_DS058243,,,,,,,,,C4012409,,300943,MONDO:0010492,"pituitary adenoma, growth hormone-secreting, 2",
+BMGC_DS15443,BMG_DS058245,,"ALACRIMA, CONGENITAL, AUTOSOMAL RECESSIVE",,,,,,,C4012597,,601549,MONDO:0011105,"alacrima, congenital, autosomal recessive",
+BMGC_DS15444,BMG_DS058246,,MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 1,,,,,,,C4012727,,603157;603387,MONDO:0011313,megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1,
+BMGC_DS15445,BMG_DS058247,,,,,,,,,C4012790,,604391,MONDO:0024557,ataxia-telangiectasia-like disorder 1,
+BMGC_DS15446,BMG_DS058255,,,,,,,,,C4013473,,611136,MONDO:0012627,"epilepsy, idiopathic generalized, susceptibility to, 13",
+BMGC_DS15447,BMG_DS058256,,,,,,,,,C4013560,,,MONDO:0800345,"atrial fibrillation, familial, 17",
+BMGC_DS15448,BMG_DS058258,,Progressive pulmonary failure,,,,,,,C4013572,,MTHU068873,,,
+BMGC_DS15449,BMG_DS058261,,"POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL",,,,,DOID:0080923,bilateral parasagittal parieto-occipital polymicrogyria,C4013648,,609390;612691,MONDO:0012986,bilateral parasagittal parieto-occipital polymicrogyria,
+BMGC_DS15450,BMG_DS058262,,,,,,,,,C4013699,,,MONDO:0800349,"atrial fibrillation, familial, 16",
+BMGC_DS15451,BMG_DS058263,,,,,,,,,C4013764,,613670,MONDO:0013352,intellectual disability-severe speech delay-mild dysmorphism syndrome,
+BMGC_DS15452,BMG_DS058265,,IMMUNODEFICIENCY 28,,,,,DOID:0111995,immunodeficiency 28,C4013947,,147569;614889,MONDO:0013953,immunodeficiency 28,
+BMGC_DS15453,BMG_DS058266,,IMMUNODEFICIENCY 29,,,,,DOID:0111950,immunodeficiency 29,C4013948,,614890;161561,MONDO:0013954,Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency,
+BMGC_DS15454,BMG_DS058267,,IMMUNODEFICIENCY 30,,,,,DOID:0111990,immunodeficiency 30,C4013949,,601604;614891,MONDO:0013955,Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency,
+BMGC_DS15455,BMG_DS058268,,IMMUNODEFICIENCY 31A,,,,,DOID:0111945,immunodeficiency 31A,C4013950,,614892;600555,MONDO:0013956,Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency,
+BMGC_DS15456,BMG_DS058274,,IMMUNODEFICIENCY 22,,,,,DOID:0111937,immunodeficiency 22,C4014233,,615758;153390,MONDO:0014334,severe combined immunodeficiency due to LCK deficiency,
+BMGC_DS15457,BMG_DS058275,,"MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY",,,,,,,C4014239,,615760;603727,MONDO:0014335,diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome,
+BMGC_DS15458,BMG_DS058276,,"ATRIAL FIBRILLATION, FAMILIAL, 15",,,,,,,C4014269,,615770,MONDO:0014340,"atrial fibrillation, familial, 15",
+BMGC_DS15459,BMG_DS058277,,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6",,,,,DOID:0090136,complex cortical dysplasia with other brain malformations 6,C4014283,,615771;191130,MONDO:0014341,complex cortical dysplasia with other brain malformations 6,
+BMGC_DS15460,BMG_DS058278,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 1,,,,,,,C4014291,,615774;195000,MONDO:0014342,female infertility due to zona pellucida defect,
+BMGC_DS15461,BMG_DS058279,,DESBUQUOIS DYSPLASIA 2,,,,,,,C4014294,,615777;608124,MONDO:0014343,Desbuquois dysplasia 2,
+BMGC_DS15462,BMG_DS058280,,"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4",,,,,,,C4014310,,107773;615779,MONDO:0014344,"congenital heart defects, multiple types, 4",
+BMGC_DS15463,BMG_DS058281,,RETINITIS PIGMENTOSA 69,,,,,,,C4014312,,615757;615780,MONDO:0014345,retinitis pigmentosa 69,
+BMGC_DS15464,BMG_DS058283,,WHITE SPONGE NEVUS 2,,,,,DOID:0081288,white sponge nevus 2,C4014321,,148065;615785,MONDO:0014346,white sponge nevus 2,
+BMGC_DS15465,BMG_DS058284,,"ROTHMUND-THOMSON SYNDROME, TYPE 3",,,,,,,C4014339,,604594;615789,MONDO:0014347,"Rothmund-Thomson syndrome, type 3",
+BMGC_DS15466,BMG_DS058285,,"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FEATURES, SPASTICITY, AND BRAIN ABNORMALITIES",,,,,,,C4014343,,611655;615802,MONDO:0014348,"intellectual disability, autosomal recessive 42",
+BMGC_DS15467,BMG_DS058286,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 9",,,,,,,C4014354,,102771;615809,MONDO:0014351,pontocerebellar hypoplasia type 9,
+BMGC_DS15468,BMG_DS058287,,ABDOMINAL OBESITY-METABOLIC SYNDROME 3,,,,,DOID:0060612,abdominal obesity-metabolic syndrome 3,C4014361,,604556;615812,MONDO:0014352,abdominal obesity-metabolic syndrome 3,
+BMGC_DS15469,BMG_DS058288,,IMMUNODEFICIENCY 23,,,,,DOID:0111953,immunodeficiency 23,C4014371,,615816;216920;615816;172100,MONDO:0014353,immunodeficiency 23,
+BMGC_DS15470,BMG_DS058289,,,,,,,,,C4014386,,615817,MONDO:0014354,"intellectual disability, autosomal recessive 43",
+BMGC_DS15471,BMG_DS058290,,"CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS",,,,,,,C4014393,,615821;125647,MONDO:0014355,"cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis",
+BMGC_DS15472,BMG_DS058291,,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7",,,,,DOID:0080116,mitochondrial complex III deficiency nuclear type 7,C4014408,,615824;614461,MONDO:0014356,mitochondrial complex III deficiency nuclear type 7,
+BMGC_DS15473,BMG_DS058292,,VULTO-VAN SILFHOUT-DE VRIES SYNDROME,,,,,DOID:0070054,Vulto-van Silfout-de Vries syndrome,C4014414,,615828;602635,MONDO:0014357,"intellectual disability, autosomal dominant 24",
+BMGC_DS15474,BMG_DS058293,774068004,"AHDC1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome",,,,,,,C4014419,,615829,MONDO:0014358,AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome,"AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome | Xia Gibbs syndrome | AHDC1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome | AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnoea, mild dysmorphism syndrome | AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome (disorder) | AHDC1-related intellectual disability, obstructive sleep apnoea, mild dysmorphism syndrome"
+BMGC_DS15475,BMG_DS058294,,"PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4",,,,,DOID:0070549,primary pigmented nodular adrenocortical disease 4,C4014425,,615830,MONDO:0014359,"pigmented nodular adrenocortical disease, primary, 4",
+BMGC_DS15476,BMG_DS058295,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 21,,,,,DOID:0080443,developmental and epileptic encephalopathy 21,C4014430,,611623;615833,MONDO:0014360,"developmental and epileptic encephalopathy, 21",
+BMGC_DS15477,BMG_DS058296,,,,,,,,,C4014435,,615834,MONDO:0014361,autism spectrum disorder due to AUTS2 deficiency,
+BMGC_DS15478,BMG_DS058298,,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8",,,,,DOID:0080117,mitochondrial complex III deficiency nuclear type 8,C4014440,,615838;615831,MONDO:0014364,mitochondrial complex III deficiency nuclear type 8,
+BMGC_DS15479,BMG_DS058299,,SPERMATOGENIC FAILURE 13,,,,,DOID:0070182,spermatogenic failure 13,C4014449,,601689;615841,MONDO:0014365,spermatogenic failure 13,
+BMGC_DS15480,BMG_DS058300,,SPERMATOGENIC FAILURE 14,,,,,DOID:0070179,spermatogenic failure 14,C4014454,,614312;615842,MONDO:0014366,spermatogenic failure 14,
+BMGC_DS15481,BMG_DS058301,,,,,,,,,C4014476,,615848;616568,MONDO:0014368,tumor predisposition syndrome 3,
+BMGC_DS15482,BMG_DS058302,,,,,,,,,C4014479,,615849,MONDO:0014369,postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome,
+BMGC_DS15483,BMG_DS058303,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 2E",,,,,DOID:0060271,pontocerebellar hypoplasia type 2E,C4014488,,615850;615851,MONDO:0014370,pontocerebellar hypoplasia type 2E,
+BMGC_DS15484,BMG_DS058304,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 23,,,,,DOID:0080415,developmental and epileptic encephalopathy 23,C4014492,,615859;615730,MONDO:0014371,"developmental and epileptic encephalopathy, 23",
+BMGC_DS15485,BMG_DS058305,,CONE-ROD DYSTROPHY 19,,,,,DOID:0111025,cone-rod dystrophy 19,C4014501,,612268;615860,MONDO:0014372,cone-rod dystrophy 19,
+BMGC_DS15486,BMG_DS058306,,"NEPHROTIC SYNDROME, TYPE 10",,,,,DOID:0080386,nephrotic syndrome type 10,C4014507,,602334;615861,MONDO:0014373,"nephrotic syndrome, type 10",
+BMGC_DS15487,BMG_DS058307,,"DIARRHEA 7, PROTEIN-LOSING ENTEROPATHY TYPE",,,,,,,C4014516,,604900;615863,MONDO:0014375,congenital diarrhea 7 with exudative enteropathy,
+BMGC_DS15488,BMG_DS058308,,COFFIN-SIRIS SYNDROME 9,,,,,DOID:0070057,Coffin-Siris syndrome 9,C4014528,,615866,MONDO:0014376,"intellectual disability, autosomal dominant 27",
+BMGC_DS15489,BMG_DS058309,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 24,,,,,DOID:0080429,developmental and epileptic encephalopathy 24,C4014531,,615871;602780,MONDO:0014377,"developmental and epileptic encephalopathy, 24",
+BMGC_DS15490,BMG_DS058310,,,,,,,,,C4014534,,615872,MONDO:0014378,primary ciliary dyskinesia 29,
+BMGC_DS15491,BMG_DS058311,766824003,"ADNP-related multiple congenital anomalies, intellectual disability, autism spectrum disorder",,,,,,,C4014538,,615873,MONDO:0014379,ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder,"Helsmoortel-van der Aa syndrome | ADNP-related multiple congenital anomalies, intellectual disability, autism spectrum disorder | Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder (disorder) | Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder"
+BMGC_DS15492,BMG_DS058312,,MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME,,,,,DOID:0111802,syndromic microphthalmia 14,C4014540,,604357;615877,MONDO:0014380,colobomatous microphthalmia-rhizomelic dysplasia syndrome,
+BMGC_DS15493,BMG_DS058313,768843007,Tatton Brown Rahman syndrome,,,,,,,C4014545,,615879,MONDO:0014382,Tatton-Brown-Rahman overgrowth syndrome,"Tatton Brown Rahman overgrowth syndrome | DNA methyltransferase 3 alpha overgrowth syndrome | Tall stature, intellectual disability, facial dysmorphism syndrome (disorder) | DNMT3A-related overgrowth syndrome | Tatton Brown Rahman syndrome | Tall stature, intellectual disability, facial dysmorphism syndrome"
+BMGC_DS15494,BMG_DS058314,,"MYOPATHY, TUBULAR AGGREGATE, 2",,,,,DOID:0080686,tubular aggregate myopathy 2,C4014557,,610277;615883,MONDO:0014383,"myopathy, tubular aggregate, 2",
+BMGC_DS15495,BMG_DS058315,,HYPOTRICHOSIS 12,,,,,DOID:0110709,hypotrichosis 12,C4014563,,615885;603636,MONDO:0014384,hypotrichosis 12,
+BMGC_DS15496,BMG_DS058316,,"AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5",,,,,,,C4014578,,615887;609840,MONDO:0014385,amelogenesis imperfecta hypomaturation type 2A5,
+BMGC_DS15497,BMG_DS058317,,"BLEEDING DISORDER, PLATELET-TYPE, 18",,,,,,,C4014584,,615888;605577,MONDO:0014386,platelet-type bleeding disorder 18,
+BMGC_DS15498,BMG_DS058318,,"LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE",,,,,DOID:0070396,progressive leukoencephalopathy with ovarian failure,C4014588,,615889;612035,MONDO:0014387,"leukoencephalopathy, progressive, with ovarian failure",
+BMGC_DS15499,BMG_DS058319,,,,,,,,,C4014596,,615892,MONDO:0014388,familial median cleft of the upper and lower lips,
+BMGC_DS15500,BMG_DS058320,,POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY,,,,,,,C4014605,,615895;610924,MONDO:0014389,polyglucosan body myopathy 1 with or without immunodeficiency,
+BMGC_DS15501,BMG_DS058321,,HYPOTRICHOSIS 13,,,,,DOID:0110710,hypotrichosis 13,C4014616,,615896;608245,MONDO:0014390,hypotrichosis 13,
+BMGC_DS15502,BMG_DS058322,,IMMUNODEFICIENCY 24,,,,,DOID:0111938,immunodeficiency 24,C4014617,,615897;123860,MONDO:0014391,severe combined immunodeficiency due to CTPS1 deficiency,
+BMGC_DS15503,BMG_DS058323,,,,,,,,,C4014621,,615905,MONDO:0014392,"developmental and epileptic encephalopathy, 25",
+BMGC_DS15504,BMG_DS058324,,DIAMOND-BLACKFAN ANEMIA 13,,,,,DOID:0111889,Diamond-Blackfan anemia 13,C4014641,,615909;603633,MONDO:0014394,Diamond-Blackfan anemia 13,
+BMGC_DS15505,BMG_DS058325,,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2,,,,,DOID:0060214,frontotemporal dementia and/or amyotrophic lateral sclerosis 2,C4014648,,615911;615903,MONDO:0014395,frontotemporal dementia and/or amyotrophic lateral sclerosis 2,
+BMGC_DS15506,BMG_DS058327,,"CARDIOMYOPATHY, DILATED, 1NN",,,,,,,C4014656,,615916;164760,MONDO:0014396,dilated cardiomyopathy 1NN,
+BMGC_DS15507,BMG_DS058328,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20,,,,,DOID:0111478,combined oxidative phosphorylation deficiency 20,C4014660,,615917;612802,MONDO:0014397,combined oxidative phosphorylation defect type 20,
+BMGC_DS15508,BMG_DS058329,,ATAXIA-TELANGIECTASIA-LIKE DISORDER 2,,,,,DOID:0081385,ataxia-telangiectasia-like disorder-2,C4014676,,176740;615919,MONDO:0014399,ataxia-telangiectasia-like disorder 2,
+BMGC_DS15509,BMG_DS058330,,RETINITIS PIGMENTOSA 70,,,,,,,C4014681,,615922;607795,MONDO:0014400,retinitis pigmentosa 70,
+BMGC_DS15510,BMG_DS058331,,"EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE",,,,,DOID:0070316,Miura type epiphyseal chondrodysplasia,C4014690,,615923;108961,MONDO:0014401,tall stature-scoliosis-macrodactyly of the great toes syndrome,
+BMGC_DS15511,BMG_DS058332,,"ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY",,,,,,,C4014700,,615924;606158,MONDO:0014402,severe neurodegenerative syndrome with lipodystrophy,
+BMGC_DS15512,BMG_DS058333,,WEBB-DATTANI SYNDROME,,,,,,,C4014708,,615926;606036,MONDO:0014404,Webb-Dattani syndrome,
+BMGC_DS15513,BMG_DS058334,,"STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET",,,,,DOID:0111457,STING-associated vasculopathy with onset in infancy,C4014722,,612374;615934,MONDO:0014405,STING-associated vasculopathy with onset in infancy,
+BMGC_DS15514,BMG_DS058335,,PANCREATIC AGENESIS 2,,,,,DOID:0060988,pancreatic agenesis 2,C4014737,,615935,MONDO:0014406,pancreatic agenesis 2,
+BMGC_DS15515,BMG_DS058336,,MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2,,,,,,,C4014738,,611223;615937,MONDO:0014407,megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2,
+BMGC_DS15516,BMG_DS058338,,MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3,,,,,,,C4014742,,123833;615938,MONDO:0014408,megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3,
+BMGC_DS15517,BMG_DS058339,,,,,,,,,C4014745,,615942,MONDO:0014409,"intellectual disability, autosomal recessive 44",
+BMGC_DS15518,BMG_DS058340,,"MYOPIA 24, AUTOSOMAL DOMINANT",,,,,,,C4014762,,615946;608730,MONDO:0014411,"myopia 24, autosomal dominant",
+BMGC_DS15519,BMG_DS058341,,"HYPERLIPOPROTEINEMIA, TYPE ID",,,,,DOID:0111420,familial GPIHBP1 deficiency,C4014767,,615947;612757,MONDO:0014412,"hyperlipoproteinemia, type 1D",
+BMGC_DS15520,BMG_DS058342,,"AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1",,,,,,,C4014795,,615952;102582,MONDO:0014414,STAT3-related early-onset multisystem autoimmune disease,
+BMGC_DS15521,BMG_DS058343,,ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2,,,,,DOID:0111624,ACTH-independent macronodular adrenal hyperplasia 2,C4014803,,615954;615549,MONDO:0014416,ACTH-independent macronodular adrenal hyperplasia 2,
+BMGC_DS15522,BMG_DS058344,,"MYOPATHY, CENTRONUCLEAR, 5",,,,,DOID:0111222,centronuclear myopathy 5,C4014814,,615959,MONDO:0014418,"myopathy, centronuclear, 5",
+BMGC_DS15523,BMG_DS058345,763344007,"Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome",,,,,,,C4014821,,615960,MONDO:0014419,ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome,"Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome | Poretti Boltshauser syndrome | Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome (disorder)"
+BMGC_DS15524,BMG_DS058346,,VESICOURETERAL REFLUX 8,,,,,,,C4014831,,615963;600985,MONDO:0014422,vesicoureteral reflux 8,
+BMGC_DS15525,BMG_DS058347,,IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES,,,,,DOID:0111961,immunodeficiency 26,C4014833,,615966,MONDO:0014423,severe combined immunodeficiency due to DNA-PKcs deficiency,
+BMGC_DS15526,BMG_DS058348,,NANOPHTHALMOS 4,,,,,,,C4014848,,615972;615949,MONDO:0014426,nanophthalmos 4,
+BMGC_DS15527,BMG_DS058349,,CONE-ROD DYSTROPHY 20,,,,,DOID:0111026,cone-rod dystrophy 20,C4014856,,614784;615973,MONDO:0014427,cone-rod dystrophy 20,
+BMGC_DS15528,BMG_DS058350,,IMMUNODEFICIENCY 27B,,,,,DOID:0111956,immunodeficiency 27B,C4014863,,615978;107470,MONDO:0014429,autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency,
+BMGC_DS15529,BMG_DS058351,,,,,,,,,C4014864,,615979,MONDO:0014430,"intellectual disability, autosomal recessive 45",
+BMGC_DS15530,BMG_DS058352,1197751007,LIPE-related familial partial lipodystrophy,,,,,,,C4014869,,615980,MONDO:0014431,LIPE-related familial partial lipodystrophy,"FPLD6 - familial partial lipodystrophy type 6 | LIPE-related familial partial lipodystrophy | Lipase E, hormone sensitive type-related familial partial lipodystrophy (disorder) | Lipase E, hormone sensitive type-related familial partial lipodystrophy"
+BMGC_DS15531,BMG_DS058354,,,,,,,,,C4014918,,616001,MONDO:0014450,"breasts and/or nipples, aplasia or hypoplasia of, 2",
+BMGC_DS15532,BMG_DS058355,,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7,,,,,,,C4014925,,616002;167409,MONDO:0014451,focal segmental glomerulosclerosis 7,
+BMGC_DS15533,BMG_DS058356,,,,,,,DOID:0111949,immunodeficiency 36,C4014934,,616005,MONDO:0014453,immunodeficiency 36,
+BMGC_DS15534,BMG_DS058358,,HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2,,,,,,,C4014939,,616006;612411,MONDO:0014454,Hennekam lymphangiectasia-lymphedema syndrome 2,
+BMGC_DS15535,BMG_DS058359,1220595008,"Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome",,,,,,,C4014942,,616007,MONDO:0014455,cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome,"CAGSSS - cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome | Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome (disorder) | Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome"
+BMGC_DS15536,BMG_DS058360,,,,,,,,,C4014954,,616022,MONDO:0014456,autosomal recessive severe congenital neutropenia due to JAGN1 deficiency,
+BMGC_DS15537,BMG_DS058361,,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11,,,,,DOID:0070432,hyperphosphatasia with impaired intellectual development syndrome 5,C4014958,,616025;610275,MONDO:0014457,hyperphosphatasia with intellectual disability syndrome 5,
+BMGC_DS15538,BMG_DS058362,,FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG,,,,,DOID:0080760,Fanconi renotubular syndrome 4,C4014962,,616026,MONDO:0014458,Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young,
+BMGC_DS15539,BMG_DS058363,,ADAMS-OLIVER SYNDROME 5,,,,,,,C4014970,,616028;190198,MONDO:0014459,Adams-Oliver syndrome 5,
+BMGC_DS15540,BMG_DS058365,764995008,"Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome",,,,,,,C4014987,,616029,MONDO:0014460,nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome,"Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome | Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome (disorder) | Ectodermal dysplasia short stature syndrome | Short stature, nail dysplasia, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome"
+BMGC_DS15541,BMG_DS058366,,HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA,,,,,,,C4014988,,616030,MONDO:0014461,hypogonadotropic hypogonadism 22 with or without anosmia,
+BMGC_DS15542,BMG_DS058367,,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8,,,,,,,C4014993,,616032;616027,MONDO:0014462,focal segmental glomerulosclerosis 8,
+BMGC_DS15543,BMG_DS058368,,"MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1",,,,,,,C4014997,,616013;616033,MONDO:0000208,"microcephaly, short stature, and impaired glucose metabolism 1",
+BMGC_DS15544,BMG_DS058371,,"CILIARY DYSKINESIA, PRIMARY, 30",,,,,,,C4015016,,616037;615956,MONDO:0014465,primary ciliary dyskinesia 30,
+BMGC_DS15545,BMG_DS058372,,NEU-LAXOVA SYNDROME 2,,,,,DOID:0080075,Neu-Laxova syndrome 2,C4015019,,616038;610936,MONDO:0014466,Neu-Laxova syndrome 2,
+BMGC_DS15546,BMG_DS058373,,"MYASTHENIC SYNDROME, CONGENITAL, 7A, PRESYNAPTIC, AND DISTAL MOTOR NEUROPATHY, AUTOSOMAL DOMINANT",,,,,DOID:0110659,congenital myasthenic syndrome 7,C4015038,,616040;600104,MONDO:0014468,congenital myasthenic syndrome 7,
+BMGC_DS15547,BMG_DS058374,,"DEAFNESS, AUTOSOMAL RECESSIVE 103",,,,,,,C4015050,,616042;607293,MONDO:0014469,autosomal recessive nonsyndromic hearing loss 103,
+BMGC_DS15548,BMG_DS058376,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22,,,,,DOID:0111498,combined oxidative phosphorylation deficiency 22,C4015062,,616045;164360,MONDO:0020727,combined oxidative phosphorylation deficiency 22,
+BMGC_DS15549,BMG_DS058377,,,,,,,,,C4015067,,616050,MONDO:0014472,periodic fever-infantile enterocolitis-autoinflammatory syndrome,
+BMGC_DS15550,BMG_DS058378,,"MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE",,,,,DOID:0070283,primary autosomal recessive microcephaly 13,C4015080,,616051;117143,MONDO:0014473,"microcephaly 13, primary, autosomal recessive",
+BMGC_DS15551,BMG_DS058382,773495009,Episodic ataxia with slurred speech,,,,,,,C4015108,,616055,MONDO:0014476,episodic ataxia type 8,Episodic ataxia with slurred speech | Episodic ataxia with slurred speech (disorder) | Episodic ataxia type 8
+BMGC_DS15552,BMG_DS058383,,,,,,,,,C4015119,,616056,MONDO:0014477,"developmental and epileptic encephalopathy, 26",
+BMGC_DS15553,BMG_DS058384,,MIRROR MOVEMENTS 3,,,,,,,C4015124,,616059;610565,MONDO:0014478,mirror movements 3,
+BMGC_DS15554,BMG_DS058385,,"POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE",,,,,,,C4015128,,616063;612107,MONDO:0014479,"porokeratosis 8, disseminated superficial actinic type",
+BMGC_DS15555,BMG_DS058386,,"46,XY SEX REVERSAL 9",,,,,DOID:0111770,"46,XY sex reversal 9",C4015129,,616067;603693,MONDO:0014480,"46,XY sex reversal 9",
+BMGC_DS15556,BMG_DS058387,,"INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2",,,,,,,C4015130,,616069;131550,MONDO:0014481,"inflammatory skin and bowel disease, neonatal, 2",
+BMGC_DS15557,BMG_DS058388,,,,,,,,,C4015141,,616078,MONDO:0014482,"intellectual disability, autosomal dominant 29",
+BMGC_DS15558,BMG_DS058389,,,,,,,,,C4015146,,616079,MONDO:0014483,retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies,
+BMGC_DS15559,BMG_DS058390,,"MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE",,,,,DOID:0070284,primary autosomal recessive microcephaly 12,C4015156,,616080;603368,MONDO:0014484,"microcephaly 12, primary, autosomal recessive",
+BMGC_DS15560,BMG_DS058391,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 1C",,,,,DOID:0112334,pontocerebellar hypoplasia type 1C,C4015160,,616081;606019,MONDO:0014485,"pontocerebellar hypoplasia, type 1C",
+BMGC_DS15561,BMG_DS058392,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 30, WITH SPEECH DELAY AND BEHAVIORAL ABNORMALITIES",,,,,DOID:0070060,autosomal dominant intellectual developmental disorder 30,C4015167,,616083;608668,MONDO:0014486,"intellectual disability, autosomal dominant 30",
+BMGC_DS15562,BMG_DS058393,,"SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY",,,,,DOID:0080209,"sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay",C4015172,,616084;612907,MONDO:0014487,congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome,
+BMGC_DS15563,BMG_DS058394,,TYPE 2 DIABETES 5,,,,,,,C4015183,,616087,MONDO:0014488,"diabetes mellitus, noninsulin-dependent, 5",
+BMGC_DS15564,BMG_DS058395,1234819007,Limb girdle muscular dystrophy due to POMK deficiency,,,,,,,C4015184,,616094,MONDO:0014489,limb-girdle muscular dystrophy due to POMK deficiency,Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency | Limb girdle muscular dystrophy due to POMK deficiency | Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency (disorder)
+BMGC_DS15565,BMG_DS058396,1216941002,Ketoacidosis due to monocarboxylate transporter-1 deficiency,,,,,,,C4015186,,616095,MONDO:0014490,ketoacidosis due to monocarboxylate transporter-1 deficiency,Ketoacidosis due to monocarboxylate transporter-1 deficiency (disorder) | Ketoacidosis due to monocarboxylate transporter-1 deficiency
+BMGC_DS15566,BMG_DS058397,,IMMUNODEFICIENCY 37,,,,,DOID:0111939,immunodeficiency 37,C4015195,,616098;603517,MONDO:0014491,immunodeficiency 37,
+BMGC_DS15567,BMG_DS058398,,PALMOPLANTAR KERATODERMA AND WOOLLY HAIR,,,,,DOID:0070554,palmoplantar keratoderma and woolly hair,C4015202,,616099;614610,MONDO:0014492,wooly hair-palmoplantar keratoderma syndrome,
+BMGC_DS15568,BMG_DS058399,,,,,,,,,C4015214,,616100,MONDO:0014493,autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency,
+BMGC_DS15569,BMG_DS058401,,,,,,,,,C4015235,,616106,MONDO:0014494,"psoriasis 15, pustular, susceptibility to",
+BMGC_DS15570,BMG_DS058402,1220597000,"Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome",,,,,,,C4015242,,616108,MONDO:0014495,retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome,"Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome (disorder) | Retinal dystrophy, juvenile cataract, short stature syndrome"
+BMGC_DS15571,BMG_DS058403,,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9",,,,,DOID:0080118,mitochondrial complex III deficiency nuclear type 9,C4015253,,616111;616097,MONDO:0014496,mitochondrial complex III deficiency nuclear type 9,
+BMGC_DS15572,BMG_DS058404,1260449002,Polyendocrine polyneuropathy syndrome,,,,,,,C4015261,,616113,MONDO:0014497,polyendocrine-polyneuropathy syndrome,Polyendocrine polyneuropathy syndrome (disorder) | Polyendocrine polyneuropathy syndrome | PEPNS - polyendocrine polyneuropathy syndrome
+BMGC_DS15573,BMG_DS058405,,FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4,,,,,,,C4015276,,606831;616115,MONDO:0014498,familial cold autoinflammatory syndrome 4,
+BMGC_DS15574,BMG_DS058406,,,,,,,,,C4015283,,616116,MONDO:0014499,"intellectual disability, autosomal recessive 46",
+BMGC_DS15575,BMG_DS058407,,CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY,,,,,,,C4015285,,616117;613932,MONDO:0014500,atrial conduction disease,
+BMGC_DS15576,BMG_DS058408,,"MACULAR DEGENERATION, EARLY-ONSET",,,,,,,C4015286,,616118;612570,MONDO:0014501,"macular degeneration, early-onset",
+BMGC_DS15577,BMG_DS058409,,IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION,,,,,DOID:0111934,immunodeficiency 38,C4015293,,616126;147571,MONDO:0014502,Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency,
+BMGC_DS15578,BMG_DS058411,1237625002,Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency,,,,,,,C4015301,,616127,MONDO:0014503,autosomal recessive spinocerebellar ataxia 17,Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency (disorder) | Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency | SCAR17 - spinocerebellar ataxia autosomal recessive type 17 | Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency
+BMGC_DS15579,BMG_DS058412,,PERRAULT SYNDROME 5,,,,,,,C4015307,,616138;606075,MONDO:0014504,Perrault syndrome 5,
+BMGC_DS15580,BMG_DS058413,,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27",,,,,DOID:0080444,developmental and epileptic encephalopathy 27,C4015316,,616139,MONDO:0014505,"developmental and epileptic encephalopathy, 27",
+BMGC_DS15581,BMG_DS058414,1220600004,RARS-related autosomal recessive hypomyelinating leukodystrophy,,,,,,,C4015323,,616140,MONDO:0014506,hypomyelinating leukodystrophy 9,Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | RARS-related autosomal recessive hypomyelinating leucodystrophy | Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy (disorder) | RARS-related autosomal recessive hypomyelinating leukodystrophy | Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leucodystrophy
+BMGC_DS15582,BMG_DS058416,,"MACULAR DYSTROPHY, VITELLIFORM, 4",,,,,,,C4015342,,616151;602870,MONDO:0014508,vitelliform macular dystrophy 4,
+BMGC_DS15583,BMG_DS058417,,"MACULAR DYSTROPHY, VITELLIFORM, 5",,,,,,,C4015343,,607056;616152,MONDO:0014509,vitelliform macular dystrophy 5,
+BMGC_DS15584,BMG_DS058418,1237619001,Fatty acyl-CoA reductase 1 deficiency,,,,,,,C4015344,,616154,MONDO:0014510,fatty acyl-CoA reductase 1 deficiency,Fatty acyl-coenzyme A reductase 1 deficiency (disorder) | FAR1 deficiency | Fatty acyl-CoA reductase 1 deficiency | PFCRD - peroxisomal fatty acyl-CoA reductase 1 disorder | Fatty acyl-coenzyme A reductase 1 deficiency
+BMGC_DS15585,BMG_DS058419,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S",,,,,DOID:0110171,Charcot-Marie-Tooth disease axonal type 2S,C4015349,,616155;600502,MONDO:0014511,Charcot-Marie-Tooth disease axonal type 2S,
+BMGC_DS15586,BMG_DS058420,,"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES",,,,,DOID:0070061,autosomal dominant intellectual developmental disorder 31,C4015357,,616158;600473,,,
+BMGC_DS15587,BMG_DS058421,,NEMALINE MYOPATHY 10,,,,,DOID:0110931,nemaline myopathy 10,C4015360,,616165;616112,MONDO:0014513,nemaline myopathy 10,
+BMGC_DS15588,BMG_DS058422,,"AORTIC ANEURYSM, FAMILIAL THORACIC 9",,,,,,,C4015368,,616166;601103,MONDO:0014514,"aortic aneurysm, familial thoracic 9",
+BMGC_DS15589,BMG_DS058423,,MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT,,,,,,,C4015371,,616170;611124,MONDO:0014515,macular dystrophy with central cone involvement,
+BMGC_DS15590,BMG_DS058424,,"MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2",,,,,DOID:0080106,microcephaly and chorioretinopathy 2,C4015388,,616171;605031,MONDO:0014516,microcephaly and chorioretinopathy 2,
+BMGC_DS15591,BMG_DS058425,,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9",,,,,DOID:0111301,generalized epilepsy with febrile seizures plus 9,C4015395,,601485;616172,MONDO:0014517,"generalized epilepsy with febrile seizures plus, type 9",
+BMGC_DS15592,BMG_DS058426,,"BLEEDING DISORDER, PLATELET-TYPE, 19",,,,,,,C4015405,,176893;616176,MONDO:0014518,platelet-type bleeding disorder 19,
+BMGC_DS15593,BMG_DS058427,,OVARIAN DYSGENESIS 4,,,,,DOID:0080496,ovarian dysgenesis 4,C4015409,,610098;616185,MONDO:0014520,"46,XX ovarian dysgenesis-short stature syndrome",
+BMGC_DS15594,BMG_DS058428,1208939001,Progressive myoclonic epilepsy type 7,,,,,DOID:0111447,progressive myoclonus epilepsy 7,C4015420,,616187,MONDO:0014521,progressive myoclonic epilepsy type 7,Progressive myoclonus epilepsy type 7 | Progressive myoclonic epilepsy due to KV3.1 deficiency | Progressive myoclonic epilepsy type 7 | EPM7 - epilepsy progressive myoclonic 7 | Progressive myoclonic epilepsy type 7 (disorder)
+BMGC_DS15595,BMG_DS058429,,RETINAL DYSTROPHY AND OBESITY,,,,,,,C4015424,,601197;616188,MONDO:0014522,retinal dystrophy and obesity,
+BMGC_DS15596,BMG_DS058430,1255271005,"Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome",,,,,,,C4015436,,616192,MONDO:0014523,juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome,"Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome (disorder) | Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome | Combined cerebellar and peripheral ataxia, deafness, diabetes mellitus syndrome | Combined cerebellar and peripheral ataxia, hearing loss, diabetes mellitus syndrome"
+BMGC_DS15597,BMG_DS058432,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 47",,,,,DOID:0081211,autosomal recessive intellectual developmental disorder 47,C4015444,,606373;616193,MONDO:0014524,"intellectual disability, autosomal recessive 47",
+BMGC_DS15598,BMG_DS058433,1228849007,Polyglucosan body myopathy type 2,,,,,,,C4015452,,616199,MONDO:0014526,polyglucosan body myopathy type 2,Polyglucosan body myopathy type 2 | Polyglucosan body myopathy type 2 (disorder) | PGBM2 - polyglucosan body myopathy type 2
+BMGC_DS15599,BMG_DS058434,1216939003,"Progeroid features, hepatocellular carcinoma predisposition syndrome",,,,,,,C4015461,,616200,MONDO:0014527,progeroid features-hepatocellular carcinoma predisposition syndrome,"Progeroid features, hepatocellular carcinoma predisposition syndrome | Ruijs Aalfs syndrome | Progeroid features, hepatocellular carcinoma predisposition syndrome (disorder)"
+BMGC_DS15600,BMG_DS058435,720507006,Chronic atrial and intestinal dysrhythmia,,,,,,,C4015474,,616201,MONDO:0014528,chronic atrial and intestinal dysrhythmia,Chronic atrial and intestinal dysrhythmia (disorder) | Chronic atrial and intestinal dysrhythmia | CAID (chronic atrial and intestinal dysrhythmia) syndrome
+BMGC_DS15601,BMG_DS058437,,CEREBELLOFACIODENTAL SYNDROME,,,,,DOID:0080898,cerebellofaciodental syndrome,C4015495,,604902;616202,MONDO:0014529,cerebellar-facial-dental syndrome,
+BMGC_DS15602,BMG_DS058438,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18",,,,,DOID:0080042,autosomal recessive spinocerebellar ataxia 18,C4015505,,616204;602368,MONDO:0014530,autosomal recessive spinocerebellar ataxia 18,
+BMGC_DS15603,BMG_DS058439,,AMYOTROPHIC LATERAL SCLEROSIS 22 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA,,,,,DOID:0060355,amyotrophic lateral sclerosis type 22,C4015512,,616208,MONDO:0014531,amyotrophic lateral sclerosis type 22,
+BMGC_DS15604,BMG_DS058440,1222644009,Autosomal dominant mitochondrial myopathy with exercise intolerance,,,,,,,C4015513,,616209,MONDO:0014532,autosomal dominant mitochondrial myopathy with exercise intolerance,Autosomal dominant mitochondrial myopathy with exercise intolerance | Autosomal dominant mitochondrial myopathy with exercise intolerance (disorder)
+BMGC_DS15605,BMG_DS058441,,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28",,,,,DOID:0080452,developmental and epileptic encephalopathy 28,C4015519,,616211,MONDO:0014533,"developmental and epileptic encephalopathy, 28",
+BMGC_DS15606,BMG_DS058442,,,,,,,,,C4015525,,616212,MONDO:0014534,lissencephaly 6 with microcephaly,
+BMGC_DS15607,BMG_DS058443,,THROMBOCYTOPENIA 5,,,,,,,C4015537,,616216;600618,MONDO:0014536,thrombocytopenia 5,
+BMGC_DS15608,BMG_DS058444,,NEPHRONOPHTHISIS 19,,,,,DOID:0111126,nephronophthisis 19,C4015542,,616217;605755,MONDO:0014537,nephronophthisis 19,
+BMGC_DS15609,BMG_DS058445,,"FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 5",,,,,DOID:0081020,congenital fibrosis of the extraocular muscles 5,C4015552,,610004;616219,MONDO:0014538,"fibrosis of extraocular muscles, congenital, 5",
+BMGC_DS15610,BMG_DS058446,,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 9,,,,,,,C4015555,,609720;616220,MONDO:0014539,focal segmental glomerulosclerosis 9,
+BMGC_DS15611,BMG_DS058447,,"AMELOGENESIS IMPERFECTA, TYPE IH",,,,,,,C4015557,,147558;616221,MONDO:0014540,amelogenesis imperfecta type 1H,
+BMGC_DS15612,BMG_DS058448,778012003,Temple syndrome,,,,,DOID:0111713,Temple syndrome,C4015558,C000726750,616222,MONDO:0014541,motor developmental delay due to 14q32.2 paternally expressed gene defect,Temple syndrome (disorder) | Temple syndrome
+BMGC_DS15613,BMG_DS058449,,"MYASTHENIC SYNDROME, CONGENITAL, 15",,,,,DOID:0110658,congenital myasthenic syndrome 15,C4015596,,612866;616227,MONDO:0014542,congenital myasthenic syndrome 15,
+BMGC_DS15614,BMG_DS058450,,"MYASTHENIC SYNDROME, CONGENITAL, 14",,,,,DOID:0110669,congenital myasthenic syndrome 14,C4015597,,607905;616228,MONDO:0014543,congenital myasthenic syndrome 14,
+BMGC_DS15615,BMG_DS058451,,"OSTEOGENESIS IMPERFECTA, TYPE XVI",,,,,,,C4015610,,616215;616229,MONDO:0014544,osteogenesis imperfecta type 16,
+BMGC_DS15616,BMG_DS058452,,"MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES",,,,,,,C4015624,,114250;616231,MONDO:0014546,myopathy due to calsequestrin and SERCA1 protein overload,
+BMGC_DS15617,BMG_DS058453,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T",,,,,,,C4015635,,617017;617017;616233;120520,MONDO:0014866,Charcot-Marie-Tooth disease axonal type 2T,
+BMGC_DS15618,BMG_DS058454,1222680009,Combined oxidative phosphorylation defect type 24,,,,,,,C4015643,,616239,MONDO:0014547,combined oxidative phosphorylation defect type 24,Combined oxidative phosphorylation defect type 24 | Combined oxidative phosphorylation defect type 24 (disorder) | COXPD24 - combined oxidative phosphorylation defect type 24
+BMGC_DS15619,BMG_DS058455,,LONG QT SYNDROME 14,,,,,,,C4015671,,616247;114180,MONDO:0014548,long QT syndrome 14,
+BMGC_DS15620,BMG_DS058456,,LETHAL CONGENITAL CONTRACTURE SYNDROME 6,,,,,,,C4015686,,616248;613915,MONDO:0014549,lethal congenital contracture syndrome 6,
+BMGC_DS15621,BMG_DS058457,,LONG QT SYNDROME 15,,,,,,,C4015695,,616249;114182,MONDO:0014550,long QT syndrome 15,
+BMGC_DS15622,BMG_DS058458,1237342004,Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome,,,,,,,C4015701,,616258,MONDO:0014552,lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome,Lethal fetal cerebrorenogenitourinary agenesis or hypoplasia syndrome | Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome | Lethal fetal cerebrorenogenitourinary agenesis or hypoplasia syndrome (disorder) | Lethal foetal cerebrorenogenitourinary agenesis/hypoplasia syndrome
+BMGC_DS15623,BMG_DS058459,,TENORIO SYNDROME,,,,,,,C4015710,,610432;616260,MONDO:0014553,Tenorio syndrome,
+BMGC_DS15624,BMG_DS058460,,"NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET 1",,,,,,,C4015728,,616263;608625,MONDO:8000012,"neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1",
+BMGC_DS15625,BMG_DS058461,,PEELING SKIN SYNDROME 3,,,,,DOID:0070522,peeling skin syndrome 3,C4015729,,616265,MONDO:0014555,peeling skin syndrome type A,
+BMGC_DS15626,BMG_DS058464,,"OSTEOGENESIS IMPERFECTA, MILD",,,,,,,C4015953,,120160,,,
+BMGC_DS15627,BMG_DS058466,763839005,Neonatal Marfan syndrome,,,,,,,C4016054,,,MONDO:0017309,neonatal Marfan syndrome,Neonatal Marfan syndrome | Neonatal Marfan syndrome (disorder)
+BMGC_DS15628,BMG_DS058469,,"ALPHA-THALASSEMIA, HMONG TYPE",,,,,,,C4016158,,141850,,,
+BMGC_DS15629,BMG_DS058470,,"EPIDERMOLYSIS BULLOSA SIMPLEX 2A, GENERALIZED SEVERE",,,,,,,C4016235,,148040;619555,,,
+BMGC_DS15630,BMG_DS058472,,,,,,,,,C4016255,,177650,MONDO:0100046,"exfoliation syndrome, susceptibility to",
+BMGC_DS15631,BMG_DS058474,783143001,Noonan syndrome-like disorder with juvenile myelomonocytic leukemia,,,,,,,C4016301,,,,,Noonan syndrome-like disorder with juvenile myelomonocytic leukaemia | Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (disorder) | Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | CBL (Cbl proto-oncogene) syndrome
+BMGC_DS15632,BMG_DS058475,1201862006,Autosomal recessive central core disease,,,,,,,C4016368,,,,,Autosomal recessive central core disease | Autosomal recessive central core disease (disorder) | Autosomal recessive central core myopathy
+BMGC_DS15633,BMG_DS058476,,"ANEMIA, PERINATAL HEMOLYTIC, FATAL OR NEAR-FATAL",,,,,,,C4016380,,182870;617948,,,
+BMGC_DS15634,BMG_DS058479,,"RENAL TUBULAR ACIDOSIS, DISTAL, 2, WITH PROGRESSIVE SENSORINEURAL HEARING LOSS",,,,,,,C4016429,,192132;267300,,,
+BMGC_DS15635,BMG_DS058481,,,,,,,,,C4016601,,,MONDO:0019157,myelodysplastic syndrome with ring sideroblasts,
+BMGC_DS15636,BMG_DS058484,,IMMUNODEFICIENCY 32B,,,,,DOID:0111985,immunodeficiency 32B,C4016741,,601565;226990;614894;226990,MONDO:0009194,immunodeficiency 32B,
+BMGC_DS15637,BMG_DS058485,,,,,,,,,C4016819,,261100,MONDO:0100156,Imerslund-Grasbeck syndrome type 1,
+BMGC_DS15638,BMG_DS058487,,IMERSLUND-GRASBECK SYNDROME 2,,,,,,,C4016948,,618882;605799,MONDO:0100157,Imerslund-Grasbeck syndrome type 2,
+BMGC_DS15639,BMG_DS058488,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 5",,,,,,,C4016970,,606596,,,
+BMGC_DS15640,BMG_DS058491,,"GALACTOSEMIA III, SEVERE",,,,,,,C4017048,,606953,,,
+BMGC_DS15641,BMG_DS058492,,,,,,,,,C4017127,,,MONDO:0017831,mild Canavan disease,
+BMGC_DS15642,BMG_DS058493,,"TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE",,,,,DOID:0111871,photosensitive trichothiodystrophy 3,C4017171,,616395;608780,MONDO:0014619,"trichothiodystrophy 3, photosensitive",
+BMGC_DS15643,BMG_DS058495,,,,,,,,,C4017190,,,MONDO:0800380,"17-alpha-hydroxylase/17,20-lyase deficiency, combined partial",
+BMGC_DS15644,BMG_DS058498,,"SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES",,,,,DOID:0112198,spondyloepimetaphyseal dysplasia with joint laxity type 1,C4017377,,271640,MONDO:0010075,"spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures",
+BMGC_DS15645,BMG_DS058501,,HEINZ BODY HEMOLYTIC ANEMIA,,,,,,,C4017465,,141900;141800,,,
+BMGC_DS15646,BMG_DS058502,,,,,,,,,C4017540,,607154,MONDO:0100177,"allergic rhinitis, susceptibility to",
+BMGC_DS15647,BMG_DS058520,,Mitochondrial Dysfunction,Mitochondrial Diseases,,,,,,C4021734,D028361,,,,
+BMGC_DS15648,BMG_DS058521,1208972001,Generalized myoclonic seizure,,,,,,,C4021759,,,,,Generalized myoclonic seizure | Generalised myoclonic seizure | Generalized onset myoclonic epileptic seizure (finding) | Generalised onset myoclonic epileptic seizure | Generalized onset myoclonic epileptic seizure | Generalised-onset myoclonic epileptic seizure | Generalized-onset myoclonic epileptic seizure
+BMGC_DS15649,BMG_DS058522,,,,,,,,,C4021765,,,MONDO:0002602,central nervous system disorder,
+BMGC_DS15650,BMG_DS058523,,,,,,,,,C4021780,,,MONDO:0005154,liver disorder,
+BMGC_DS15651,BMG_DS058525,,,,,,,,,C4021818,,,MONDO:0005558,ovarian disorder,
+BMGC_DS15652,BMG_DS058541,,Obstructive azoospermia,,,,,,,C4023106,,MTHU072476,,,
+BMGC_DS15653,BMG_DS058545,715734006,Thyroid hemiagenesis,,,,,,,C4023190,,,MONDO:0019860,thyroid hemiagenesis,Congenital absence of half of thyroid (disorder) | Congenital absence of half of thyroid | Congenital hemiagenesis of thyroid | Thyroid hemiagenesis
+BMGC_DS15654,BMG_DS058554,1208629005,Myoclonic absence seizure,,,,,,,C4023512,,,,,Myoclonic absence seizure | Myoclonic absence seizure (finding)
+BMGC_DS15655,BMG_DS058558,,,,,,,,,C4023704,,102350,MONDO:0007054,acromial dimples,
+BMGC_DS15656,BMG_DS058566,,,,,,,,,C4024851,,,MONDO:0017675,punctate palmoplantar keratoderma,
+BMGC_DS15657,BMG_DS058567,,,,,,,,,C4024880,,602032,MONDO:0011177,"ectodermal dysplasia 4, hair/nail type",
+BMGC_DS15658,BMG_DS058568,,Mixed demyelinating and axonal polyneuropathy,,,,,,,C4024907,,MTHU067948,,,
+BMGC_DS15659,BMG_DS058570,,Lower limb amyotrophy,,,,,,,C4024921,,MTHU055737,,,
+BMGC_DS15660,BMG_DS058573,,Proximal spinal muscular atrophy,,,,,,,C4024957,,MTHU078224,MONDO:0019079,proximal spinal muscular atrophy,
+BMGC_DS15661,BMG_DS058574,715905006,Unilateral polymicrogyria,,,,,,,C4024960,,,MONDO:0017092,unilateral polymicrogyria,Unilateral polymicrogyria (disorder) | Unilateral polymicrogyria
+BMGC_DS15662,BMG_DS058579,724597006,Vasculitis of large artery,,,,,,,C4025218,,,,,Vasculitis of large artery (disorder) | Vasculitis of large artery | Large vessel vasculitis
+BMGC_DS15663,BMG_DS058581,,Congenital lactic acidosis,,,,,,,C4025276,,MTHU073510,,,
+BMGC_DS15664,BMG_DS058582,,,,,,,,,C4025295,,139600,MONDO:0007693,hypertrichosis cubiti-short stature syndrome,
+BMGC_DS15665,BMG_DS058586,,,,,,,,,C4025790,,,MONDO:0016225,specific learning disability,
+BMGC_DS15666,BMG_DS058588,,,,,,,,,C4025831,,,MONDO:0003620,peripheral nervous system disorder,
+BMGC_DS15667,BMG_DS058589,,,,,,,,,C4025836,,,MONDO:0001898,optic choroid disorder,
+BMGC_DS15668,BMG_DS058621,,Asthma-Chronic Obstructive Pulmonary Disease Overlap Syndrome,Asthma-Chronic Obstructive Pulmonary Disease Overlap Syndrome,,,,,,C4038730,D000080445,,,,
+BMGC_DS15669,BMG_DS058636,1082711000119108,Gastric hemorrhage due to angiodysplasia of stomach,,,,,,,C4038767,,,,,Gastric hemorrhage due to angiodysplasia of stomach (disorder) | Gastric hemorrhage due to angiodysplasia of stomach | Gastric haemorrhage due to angiodysplasia of stomach
+BMGC_DS15670,BMG_DS058840,,Acute Hypoxemic Respiratory Failure,Respiratory Insufficiency,,,,,,C4039867,D012131,,,,
+BMGC_DS15671,BMG_DS058948,,Acute Hypercapnic Respiratory Failure,Respiratory Insufficiency,,,,,,C4040419,D012131,,,,
+BMGC_DS15672,BMG_DS058965,10625231000119106,Bronchopneumonia caused by Haemophilus influenzae,,,,,,,C4040491,,,,,Bronchopneumonia caused by Haemophilus influenzae | Bronchopneumonia caused by Haemophilus influenzae (disorder)
+BMGC_DS15673,BMG_DS059003,711409002,"3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome",,,,,,,C4040739,,614739,MONDO:0013875,"3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome","MEGDEL syndrome | 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome (disorder) | 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome"
+BMGC_DS15674,BMG_DS059148,,"Cone-rod synaptic disorder, congenital nonprogressive",,,,,,,C4041558,C536122,610427,MONDO:0012490,"cone-rod synaptic disorder, congenital nonprogressive",
+BMGC_DS15675,BMG_DS059341,711152006,Autosomal dominant hypocalcemia,,,,E20.810,,,C4048195,,,MONDO:0018543,autosomal dominant hypocalcemia,Autosomal dominant hypocalcemia (disorder) | Autosomal dominant hypocalcemia | Autosomal dominant hypocalcaemia | Familial hypocalcemia | Familial hypocalcaemia | Autosomal dominant hypoparathyroidism | Familial hypercalciuric hypocalcemia | Familial hypercalciuric hypocalcaemia
+BMGC_DS15676,BMG_DS059342,,beta-Mannosidosis,beta-Mannosidosis,,,,DOID:3633,beta-mannosidosis,C4048196,D044905,248510,MONDO:0009562,beta-mannosidosis,
+BMGC_DS15677,BMG_DS059343,,Hydronephrosis Due To Pujo,,,,,,,C4048262,C537373,,,,
+BMGC_DS15678,BMG_DS059344,95686007,Chorioretinal atrophy,,,,,,,C4048273,,MTHU018963,,,Chorioretinal atrophy | Chorioretinal atrophy (disorder)
+BMGC_DS15679,BMG_DS059348,,,,,,,,,C4048306,,,MONDO:0019003,multiple endocrine neoplasia type 2,
+BMGC_DS15680,BMG_DS059349,,,,,,,,,C4048328,,603956,MONDO:0002974,cervical cancer,
+BMGC_DS15681,BMG_DS059352,190708000;43123004,Hypermethioninemia,,,,,DOID:0050544,hypermethioninemia,C4048705,C564683,MTHU003943,MONDO:0000351,disorder of methionine catabolism,(Methioninemia) or (hypermethioninemia) | Methioninaemia | (Methioninaemia) or (hypermethioninaemia) | Hypermethioninemia | Hypermethioninaemia | (Methioninaemia) or (hypermethioninaemia) (disorder) | Hypermethioninemia | Hypermethioninaemia | Hypermethioninemia (disorder)
+BMGC_DS15682,BMG_DS059353,410796000,Juvenile seropositive polyarthritis,,,,,,,C4048747,,,,,"Juvenile seropositive polyarthritis (disorder) | Juvenile seropositive polyarthritis | Juvenile rheumatoid arthritis, seropositive | Juvenile idiopathic arthritis, polyarthritis, rheumatoid factor positive | Juvenile seropositive arthritis | Juvenile chronic arthritis, polyarticular seropositive"
+BMGC_DS15683,BMG_DS059354,,Sphincter of Oddi Dyskinesia,Sphincter of Oddi Dysfunction,,,,,,C4048750,D046628,,,,
+BMGC_DS15684,BMG_DS059355,,,,,,,,,C4048809,,162091,MONDO:0024517,SMARCB1-related schwannomatosis,
+BMGC_DS15685,BMG_DS059357,,CATARACT 40,,,,,,,C4049004,,302200;300457,MONDO:0010544,cataract 40,
+BMGC_DS15686,BMG_DS059359,,,,,,,,,C4049066,,616502,MONDO:0014669,cone-rod dystrophy 21,
+BMGC_DS15687,BMG_DS059360,,,,,,,,,C4049090,,109200,MONDO:0007184,"alopecia, androgenetic, 1",
+BMGC_DS15688,BMG_DS059361,717941005,Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency,,,,,,,C4049241,,,,,Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency (disorder) | Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency | PXE (pseudoxanthoma elasticum) like syndrome | Pseudoxanthoma elasticum-like syndrome
+BMGC_DS15689,BMG_DS059365,,,,,,,DOID:0070475,SMARCB1-deficient renal medullary carcinoma,C4049328,,,MONDO:0006260,kidney medullary carcinoma,
+BMGC_DS15690,BMG_DS059372,,,,,,,,,C4049650,,202200,MONDO:0024536,glucocorticoid deficiency 1,
+BMGC_DS15691,BMG_DS059373,,,,,,,,,C4049714,,607398,MONDO:0011826,glucocorticoid deficiency 2,
+BMGC_DS15692,BMG_DS059378,715727009,Pituitary stalk interruption syndrome,,,,,,,C4053775,,MTHU074262,MONDO:0019828,pituitary stalk interruption syndrome,Pituitary stalk interruption syndrome (disorder) | Pituitary stalk interruption syndrome | Ectopic neurohypophysis
+BMGC_DS15693,BMG_DS059381,,,,,,,,,C4054476,,601665,MONDO:0019182,inherited obesity,
+BMGC_DS15694,BMG_DS059382,,,,,,,DOID:3203,macrocystic neurilemmoma,C4054526,,,MONDO:0002556,microcystic/reticular schwannoma,
+BMGC_DS15695,BMG_DS059384,765326001,Familial glucocorticoid deficiency,,,,,,,C4054695,,,MONDO:0008733,familial glucocorticoid deficiency,Familial glucocorticoid deficiency (disorder) | Familial glucocorticoid deficiency
+BMGC_DS15696,BMG_DS059386,1231283007,Congenital isolated adrenocorticotropic hormone deficiency,,,,,,,C4055196,,,,,Congenital isolated adrenocorticotropic hormone deficiency (disorder) | Congenital isolated adrenocorticotropic hormone deficiency | Congenital isolated ACTH (adrenocorticotropic hormone) deficiency
+BMGC_DS15697,BMG_DS059388,,,,,,,,,C4055342,,614809,MONDO:0013892,C3 glomerulonephritis,
+BMGC_DS15698,BMG_DS059389,,,,,,,DOID:0070632,acute myeloid leukemia with MNX1-ETV6 fusion,C4055493,,,,,
+BMGC_DS15699,BMG_DS059590,369001000119100,Urinary tract infection caused by Klebsiella,,,,,,,C4076057,,,,,Urinary tract infection caused by Klebsiella | Urinary tract infection caused by Klebsiella (disorder)
+BMGC_DS15700,BMG_DS059722,,Autosomal Dominant Hereditary Pancreatitis,,,,,,,C4080064,C537262,,,,
+BMGC_DS15701,BMG_DS060005,,Hyperammonemia Due to Carbamoyl Phosphate Synthetase 1 Deficiency,Carbamoyl-Phosphate Synthase I Deficiency Disease,,,,,,C4082171,D020165,237300,MONDO:0009376,carbamoyl phosphate synthetase I deficiency disease,
+BMGC_DS15702,BMG_DS060006,65705009,Porencephalic cyst,,,,,,,C4082172,,MTHU017161,,,Porencephalic cyst | Porencephalic cyst (disorder)
+BMGC_DS15703,BMG_DS060007,193045003,Porencephaly,Porencephaly,,,,,,C4082173,D065708,MTHU007068,MONDO:0017410,porencephaly,Porencephaly | Porencephaly (disorder)
+BMGC_DS15704,BMG_DS060008,,"Thyrotropin deficiency, isolated",,,,,,,C4082174,C000610012,,,,
+BMGC_DS15705,BMG_DS060009,715795005,Charcot-Marie-Tooth disease type 4,,,,,,,C4082197,,,MONDO:0018995,Charcot-Marie-Tooth disease type 4,Autosomal recessive demyelinating Charcot-Marie-Tooth | Charcot-Marie-Tooth disease type 4 (disorder) | Charcot-Marie-Tooth disease type 4
+BMGC_DS15706,BMG_DS060011,230547002,Bulbar palsy,,,,,,,C4082299,,MTHU027729,,,Bulbar palsy | Bulbar palsy (disorder)
+BMGC_DS15707,BMG_DS060012,,Deaf Mutism,Deafness,,,,,,C4082305,D003638,,,,
+BMGC_DS15708,BMG_DS060013,402134005,Onychomycosis due to dermatophyte,,,,,,,C4082762,,,,,Onychomycosis due to dermatophyte | Tinea of nail | Tinea unguium | Dermatophytosis of nail | Onychomycosis caused by dermatophyte (disorder) | Onychomycosis caused by dermatophyte
+BMGC_DS15709,BMG_DS060017,,CHROMOSOME Xp22 DELETION SYNDROME,,,,,,,C4082794,,300830,,,
+BMGC_DS15710,BMG_DS060018,2707005,Necrotizing enterocolitis in fetus OR newborn,,,,,,,C4082937,,,MONDO:0004639,perinatal necrotizing enterocolitis,Necrotizing enterocolitis in fetus OR newborn | Pseudomembranous enterocolitis in newborn | Necrotising enterocolitis in fetus OR newborn | Necrotizing enterocolitis in fetus OR newborn (disorder) | Necrotising enterocolitis | NEC - Necrotising enterocolitis | Necrotizing enterocolitis | NEC - Necrotizing enterocolitis | Necrotising enterocolitis in foetus OR newborn
+BMGC_DS15711,BMG_DS060019,,,,,,,,,C4082951,,,MONDO:0018687,progressive muscular atrophy,
+BMGC_DS15712,BMG_DS060020,,Dupuytren's Disease,Dupuytren Contracture,,,,,,C4082974,D004387,,,,
+BMGC_DS15713,BMG_DS060021,,"Guillain-Barre Syndrome, Familial",Guillain-Barre Syndrome,,,,,,C4083008,D020275,139393,MONDO:0007691,"Guillain-Barre syndrome, familial",
+BMGC_DS15714,BMG_DS060022,,,,,,,,,C4083045,,607688,MONDO:0011896,"Parkinson disease 11, autosomal dominant, susceptibility to",
+BMGC_DS15715,BMG_DS060023,,SPONDYLOCOSTAL DYSOSTOSIS 5,,,,,DOID:0112363,spondylocostal dysostosis 5,C4083048,,122600;602427,MONDO:0007389,spondylocostal dysostosis 5,
+BMGC_DS15716,BMG_DS060025,,"Alopecia, Male Pattern",Alopecia,,,,,,C4083212,D000505,,MONDO:0800201,"baldness, male pattern",
+BMGC_DS15717,BMG_DS060026,,"Trichothiodystrophy, Nonphotosensitive 1",Trichothiodystrophy Syndromes,,,,DOID:0111868;DOID:2960,photosensitive trichothiodystrophy | nonphotosensitive trichothiodystrophy 5,C4083251,D054463,,,,
+BMGC_DS15718,BMG_DS060027,,"DEAFNESS, AUTOSOMAL DOMINANT 40",,,,,,,C4084708,,616357;123740,MONDO:0014603,autosomal dominant nonsyndromic hearing loss 40,
+BMGC_DS15719,BMG_DS060028,,"DEAFNESS, AUTOSOMAL RECESSIVE 97",,,,,,,C4084709,,164860;616705,MONDO:0014739,autosomal recessive nonsyndromic hearing loss 97,
+BMGC_DS15720,BMG_DS060029,,"DEAFNESS, AUTOSOMAL DOMINANT 67",,,,,,,C4084712,,606731;616340,MONDO:0014594,autosomal dominant nonsyndromic hearing loss 67,
+BMGC_DS15721,BMG_DS060031,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U",,,,,,,C4084821,,156560;616280,MONDO:0014566,Charcot-Marie-Tooth disease axonal type 2U,
+BMGC_DS15722,BMG_DS060032,,JOUBERT SYNDROME 23,,,,,DOID:0110992,Joubert syndrome 23,C4084822,,610178;616490,MONDO:0014664,Joubert syndrome 23,
+BMGC_DS15723,BMG_DS060033,,"MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL",,,,,DOID:0110663,congenital myasthenic syndrome 1A,C4084823,,100690;601462,,,
+BMGC_DS15724,BMG_DS060034,,"FANCONI ANEMIA, COMPLEMENTATION GROUP T",,,,,DOID:0111081,Fanconi anemia complementation group T,C4084840,,616435;610538,MONDO:0014638,Fanconi anemia complementation group T,
+BMGC_DS15725,BMG_DS060035,,JOUBERT SYNDROME 24,,,,,DOID:0110993,Joubert syndrome 24,C4084841,,616654;613846,MONDO:0014724,Joubert syndrome 24,
+BMGC_DS15726,BMG_DS060036,,JOUBERT SYNDROME 25,,,,,DOID:0110994,Joubert syndrome 25,C4084842,,616781;616690,MONDO:0014770,Joubert syndrome 25,
+BMGC_DS15727,BMG_DS060037,,JOUBERT SYNDROME 26,,,,,DOID:0110995,Joubert syndrome 26,C4084843,,616784;616650,MONDO:0014771,Joubert syndrome 26,
+BMGC_DS15728,BMG_DS060039,,MEND SYNDROME,,,,,DOID:0111865,MEND syndrome,C4085243,,300205;300960,MONDO:0010498,MEND syndrome,
+BMGC_DS15729,BMG_DS060040,,,,,,,,,C4085248,,607278;609143,MONDO:0011806,osteofibrous dysplasia,
+BMGC_DS15730,BMG_DS060041,,OPTIC ATROPHY 8,,,,,DOID:0111439,optic atrophy 8,C4085249,,616648,MONDO:0024569,optic atrophy 8,
+BMGC_DS15731,BMG_DS060042,,PAGET DISEASE OF BONE 6,,,,,DOID:0081369,Paget's disease of bone 6,C4085250,,616833;610568,MONDO:0014792,Paget disease of bone 6,
+BMGC_DS15732,BMG_DS060043,,"PAGET DISEASE OF BONE 2, EARLY-ONSET",,,,,DOID:0081365,Paget's disease of bone 2,C4085251,,602080;603499,MONDO:0011183,"Paget disease of bone 2, early-onset",
+BMGC_DS15733,BMG_DS060044,,PAGET DISEASE OF BONE 3,,,,,DOID:0081366,Paget's disease of bone 3,C4085252,,167250;601530,MONDO:0008176,Paget disease of bone 3,
+BMGC_DS15734,BMG_DS060046,,"Fibromatosis, Palmar",Dupuytren Contracture,,,,,,C4085370,D004387,,MONDO:0006345,palmar fibromatosis,
+BMGC_DS15735,BMG_DS060047,,Carbamoyl Phosphate Synthase 1 Deficiency,Carbamoyl-Phosphate Synthase I Deficiency Disease,,,,,,C4085580,D020165,,,,
+BMGC_DS15736,BMG_DS060048,,Cone-Rod Dystrophies,Cone-Rod Dystrophies,,,,,,C4085590,D000071700,,MONDO:0015993,cone-rod dystrophy,
+BMGC_DS15737,BMG_DS060049,,AL-RAQAD SYNDROME,,,,,,,C4085595,,616459;610534,MONDO:0014648,Al-Raqad syndrome,
+BMGC_DS15738,BMG_DS060050,,CHOPS SYNDROME,,,,,,,C4085597,,604417;616368,MONDO:0014609,cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome,
+BMGC_DS15739,BMG_DS060051,,LUSCAN-LUMISH SYNDROME,,,,,,,C4085873,,612778;616831,MONDO:0014791,Luscan-Lumish syndrome,
+BMGC_DS15740,BMG_DS060055,1208478005,Familial infantile bilateral striatal necrosis,,,,,,,C4087174,,271930,MONDO:0010080,familial infantile bilateral striatal necrosis,Familial infantile bilateral striatal necrosis | Familial infantile bilateral striatal necrosis (disorder) | Familial infantile striatonigral necrosis | Familial infantile striatonigral degeneration | Familial IBSN (infantile bilateral striatal necrosis)
+BMGC_DS15741,BMG_DS060060,,,,,,,,,C4087273,,,MONDO:0018013,non-immunoglobulin-mediated membranoproliferative glomerulonephritis,
+BMGC_DS15742,BMG_DS060063,,,,,,,,,C4087347,,,MONDO:0020380,autosomal dominant cerebellar ataxia,
+BMGC_DS15743,BMG_DS060068,,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1",,,,,DOID:0111522,autosomal recessive progressive external ophthalmoplegia 1,C4225153,,258450;174763,MONDO:0009783,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1",
+BMGC_DS15744,BMG_DS060069,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 9",,,,,DOID:0080359,mitochondrial complex IV deficiency nuclear type 9,C4225154,,616500;613920,MONDO:0014667,"cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3",
+BMGC_DS15745,BMG_DS060070,,"ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY",,,,,DOID:0080343,autosomal recessive pyridoxine-refractory sideroblastic anemia 3,C4225155,,616860,MONDO:0014804,sideroblastic anemia 3,
+BMGC_DS15746,BMG_DS060071,,,,,,,,,C4225156,,616351,MONDO:0014599,"intellectual disability, autosomal dominant 34",
+BMGC_DS15747,BMG_DS060072,,FAMILIAL ADENOMATOUS POLYPOSIS 3,,,,,DOID:0080411,familial adenomatous polyposis 3,C4225157,,616415;602656,MONDO:0014630,familial adenomatous polyposis 3,
+BMGC_DS15748,BMG_DS060073,1208512000,Spinocerebellar ataxia type 41,,,,,,,C4225158,,616410,MONDO:0014626,spinocerebellar ataxia type 41,Spinocerebellar ataxia type 41 | Spinocerebellar ataxia type 41 (disorder)
+BMGC_DS15749,BMG_DS060074,,"REDUCING BODY MYOPATHY, X-LINKED 1B, WITH LATE CHILDHOOD OR ADULT ONSET",,,,,DOID:0080687,reducing body myopathy 1B,C4225159,,300718;300163,MONDO:0010415,"myopathy, reducing body, X-linked, childhood-onset",
+BMGC_DS15750,BMG_DS060075,781386002,NUDT15 deficiency,,,,,,,C4225160,,,,,Deficiency of nudix hydrolase 15 | Thiopurine poor metaboliser 2 | NUDT15 deficiency | Thiopurine poor metabolizer 2 | Deficiency of nudix hydrolase 15 (disorder) | Nucleotide diphosphatase deficiency
+BMGC_DS15751,BMG_DS060076,1228858000,Complex lethal osteochondrodysplasia,,,,,,,C4225162,,616897,MONDO:0014821,complex lethal osteochondrodysplasia,Complex lethal osteochondrodysplasia (disorder) | Complex lethal osteochondrodysplasia | Complex lethal osteochondrodysplasia Symoens Barnes Gistelinck type
+BMGC_DS15752,BMG_DS060077,,MITOCHONDRIAL DNA DEPLETION SYNDROME 14 (CARDIOENCEPHALOMYOPATHIC TYPE),,,,,DOID:0080336,mitochondrial DNA depletion syndrome 14,C4225163,,616896,MONDO:0014820,mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type),
+BMGC_DS15753,BMG_DS060078,,"ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3",,,,,DOID:0060767,autosomal dominant Robinow syndrome 3,C4225164,,601368;616894,MONDO:0014819,autosomal dominant Robinow syndrome 3,
+BMGC_DS15754,BMG_DS060079,,"NEPHROTIC SYNDROME, TYPE 13",,,,,DOID:0080381,nephrotic syndrome type 13,C4225165,,614352;616893,MONDO:0014818,"nephrotic syndrome, type 13",
+BMGC_DS15755,BMG_DS060080,,"NEPHROTIC SYNDROME, TYPE 12",,,,,DOID:0080387,nephrotic syndrome type 12,C4225166,,616892;614351,MONDO:0014817,"nephrotic syndrome, type 12",
+BMGC_DS15756,BMG_DS060081,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 52",,,,,DOID:0081215,autosomal recessive intellectual developmental disorder 52,C4225168,,616887;609552,MONDO:0014815,"intellectual disability, autosomal recessive 52",
+BMGC_DS15757,BMG_DS060082,,"ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 3",,,,,DOID:0110013,advanced sleep phase syndrome 3,C4225169,,616882;603427,MONDO:0014814,advanced sleep phase syndrome 3,
+BMGC_DS15758,BMG_DS060083,,"LEUKODYSTROPHY, HYPOMYELINATING, 13",,,,,DOID:0060795,hypomyelinating leukodystrophy 13,C4225170,,614908;616881,MONDO:0014813,hypomyelinating leukodystrophy 13,
+BMGC_DS15759,BMG_DS060084,,"CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION",,,,,DOID:0081276,"cerebellar atrophy, visual impairment, and psychomotor retardation",C4225172,,616846;616875,MONDO:0014811,"cerebellar atrophy, visual impairment, and psychomotor retardation;",
+BMGC_DS15760,BMG_DS060085,,"IMMUNODEFICIENCY, COMMON VARIABLE, 13",,,,,DOID:0081155,common variable immunodeficiency 13,C4225173,,603023;616873,MONDO:0014810,pancytopenia due to IKZF1 mutations,
+BMGC_DS15761,BMG_DS060086,,,,,,,,,C4225174,,616871,MONDO:0014809,DDX41-related hematologic malignancy predisposition syndrome,
+BMGC_DS15762,BMG_DS060087,,SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2,,,,,,,C4225176,,614215;616867,MONDO:0014807,spinal muscular atrophy with congenital bone fractures 2,
+BMGC_DS15763,BMG_DS060088,,SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1,,,,,,,C4225177,,604501;271225;616866;616866,MONDO:0014806,spinal muscular atrophy with congenital bone fractures 1,
+BMGC_DS15764,BMG_DS060089,773492007,Childhood-onset spasticity with hyperglycinemia,,,,,,,C4225178,,616859,MONDO:0014803,spasticity-ataxia-gait anomalies syndrome,"Childhood-onset spasticity with hyperglycinemia (disorder) | Childhood-onset spasticity with hyperglycinaemia | Childhood-onset spasticity with hyperglycinemia | Childhood-onset spasticity with variant non-ketotic hyperglycinaemia | Spasticity, ataxia, gait anomalies syndrome | Childhood-onset spasticity with variant non-ketotic hyperglycinemia"
+BMGC_DS15765,BMG_DS060090,,COWDEN SYNDROME 7,,,,,DOID:0081003,Cowden syndrome 7,C4225179,,616858;610512,MONDO:0014802,Cowden syndrome 7,
+BMGC_DS15766,BMG_DS060091,1260203008,EVEN-plus syndrome,,,,,,,C4225180,,616854,MONDO:0014801,even-plus syndrome,"Epiphyseal, vertebral, ear dysplasia, nose plus associated findings syndrome (disorder) | EVEN-plus syndrome | Epiphyseal, vertebral, ear dysplasia, nose plus associated findings syndrome | EVEN (epiphyseal, vertebral, ear dysplasia, nose) plus associated findings syndrome"
+BMGC_DS15767,BMG_DS060092,1217226000,Progressive scapulohumeroperoneal distal myopathy,,,,,,,C4225181,,616852,MONDO:0014800,progressive scapulohumeroperoneal distal myopathy,Progressive scapulohumeroperoneal distal myopathy (disorder) | Progressive scapulohumeroperoneal distal myopathy
+BMGC_DS15768,BMG_DS060093,,CATARACT 45,,,,,,,C4225182,,616851;616655,MONDO:0014799,cataract 45,
+BMGC_DS15769,BMG_DS060094,,"BRACHYDACTYLY, TYPE A1, D",,,,,DOID:0110978,brachydactyly type A1D,C4225183,,616849;603248,MONDO:0014798,brachydactyly type A1D,
+BMGC_DS15770,BMG_DS060095,1222667006,PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis,,,,,,,C4225184,,616843,MONDO:0014797,lymphatic malformation 6,PIEZO1-related generalised lymphatic dysplasia with non-immune hydrops fetalis | Piezo type mechanosensitive ion channel component 1-related generalized lymphatic dysplasia with non-immune hydrops fetalis | Piezo type mechanosensitive ion channel component 1-related generalised lymphatic dysplasia with non-immune hydrops fetalis | PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis | Piezo type mechanosensitive ion channel component 1-related generalized lymphatic dysplasia with non-immune hydrops fetalis (disorder) | PIEZO1-related generalised lymphatic dysplasia with systemic involvement | PIEZO1-related generalized lymphatic dysplasia with systemic involvement | Generalized lymphatic dysplasia of Fotiou | Generalised lymphatic dysplasia of Fotiou | PIEZO1-related lymphatic-related hydrops fetalis
+BMGC_DS15771,BMG_DS060096,,,,,,,,,C4225186,,616840,MONDO:0014796,autosomal recessive early-onset Parkinson disease 23,
+BMGC_DS15772,BMG_DS060097,,"EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE",,,,,,,C4225187,,616839;138480,MONDO:0014795,"exercise intolerance, riboflavin-responsive",
+BMGC_DS15773,BMG_DS060098,,MEIER-GORLIN SYNDROME 6,,,,,DOID:0080517,Meier-Gorlin syndrome 6,C4225188,,616835;602842,MONDO:0014794,Meier-Gorlin syndrome 6,
+BMGC_DS15774,BMG_DS060099,1208738002,TMEM199 congenital disorder of glycosylation,,,,,,,C4225190,,616829,MONDO:0014790,TMEM199-CDG,Transmembrane protein 199 congenital disorder of glycosylation | Transmembrane protein 199 congenital disorder of glycosylation (disorder) | TMEM199 congenital disorder of glycosylation | Congenital disorder of glycosylation type IIp | TMEM199-CDG - transmembrane protein 199 congenital disorder of glycosylation | CDG (congenital disorder of glycosylation) syndrome type IIp | Carbohydrate deficient glycoprotein syndrome type IIp
+BMGC_DS15775,BMG_DS060100,1187174002,CCDC115 congenital disorder of glycosylation,,,,,,,C4225191,,616828,MONDO:0014789,CCDC115-CDG,Coiled-coil domain containing 115 congenital disorder of glycosylation | CCDC115-CDG - coiled-coil domain containing 115 congenital disorder of glycosylation | Congenital disorder of glycosylation type 2o | Congenital disorder of glycosylation type IIo | Carbohydrate deficient glycoprotein syndrome type IIo | Coiled-coil domain containing 115 congenital disorder of glycosylation (disorder) | CCDC115 congenital disorder of glycosylation
+BMGC_DS15776,BMG_DS060101,1179297007,LIMS2-related limb girdle muscular dystrophy,,,,,,,C4225192,,616827,MONDO:0014788,autosomal recessive limb-girdle muscular dystrophy type 2W,LIMS2-related limb girdle muscular dystrophy | Autosomal recessive limb girdle muscular dystrophy type 2W | LIM zinc finger domain containing 2-related limb girdle muscular dystrophy | Limb girdle muscular dystrophy type 2W | LIM zinc finger domain containing 2-related limb girdle muscular dystrophy (disorder)
+BMGC_DS15777,BMG_DS060102,1208727002,"Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome",,,,,,,C4225193,,616819,MONDO:0014787,severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome,"Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder) | Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome"
+BMGC_DS15778,BMG_DS060103,,,,,,,,,C4225194,,616818,MONDO:0014786,"IgA nephropathy, susceptibility to, 3",
+BMGC_DS15779,BMG_DS060104,,"MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2",,,,,,,C4225195,,613257;616817,MONDO:0014785,"microcephaly, short stature, and impaired glucose metabolism 2",
+BMGC_DS15780,BMG_DS060105,,"HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION",,,,,,,C4225196,,616735;616816,MONDO:0014784,severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome,
+BMGC_DS15781,BMG_DS060106,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 15,,,,,,,C4225197,,612399;616814,,,
+BMGC_DS15782,BMG_DS060107,,HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 6,,,,,DOID:0070437,hyperphosphatasia with impaired intellectual development syndrome 6,C4225201,,610662;616809,MONDO:0014780,hyperphosphatasia with intellectual disability syndrome 6,
+BMGC_DS15783,BMG_DS060108,1251453008,Lamb Shaffer syndrome,,,,,,,C4225202,,616803,MONDO:0014778,Lamb-Shaffer syndrome,SOX5 haploinsufficiency syndrome | Lamb Shaffer syndrome | Lamb Shaffer syndrome (disorder)
+BMGC_DS15784,BMG_DS060109,,"HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2",,,,,,,C4225203,,612636;616801,MONDO:0014777,"hypotonia, infantile, with psychomotor retardation and characteristic facies 2",
+BMGC_DS15785,BMG_DS060110,1208513005,Spinocerebellar ataxia type 42,,,,,,,C4225205,,616795,MONDO:0014776,spinocerebellar ataxia type 42,Spinocerebellar ataxia type 42 | Spinocerebellar ataxia type 42 (disorder)
+BMGC_DS15786,BMG_DS060111,,,,,,,,,C4225207,,616792,MONDO:0014774,"neuroblastoma, susceptibility to, 7",
+BMGC_DS15787,BMG_DS060112,,IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS,,,,,,,C4225208,,616789,MONDO:0014773,cardiac anomalies - developmental delay - facial dysmorphism syndrome,
+BMGC_DS15788,BMG_DS060113,,,,,,,,,C4225209,,616788,MONDO:0014772,orofacial cleft 15,
+BMGC_DS15789,BMG_DS060114,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 2,,,,,,,C4225210,,616768;616780,MONDO:0021573,oocyte maturation defect 2,
+BMGC_DS15790,BMG_DS060115,,"CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2",,,,,,,C4225211,,602194;616779,MONDO:0014768,"cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2",
+BMGC_DS15791,BMG_DS060116,,SECKEL SYNDROME 9,,,,,DOID:0070005,Seckel syndrome 9,C4225212,,616777;605958,MONDO:0014767,Seckel syndrome 9,
+BMGC_DS15792,BMG_DS060117,,LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA,,,,,,,C4225213,,616763;611893,MONDO:0014766,leukodystrophy and acquired microcephaly with or without dystonia;,
+BMGC_DS15793,BMG_DS060118,,"WOOLLY HAIR, AUTOSOMAL RECESSIVE 3",,,,,DOID:0111574,autosomal recessive woolly hair 3,C4225214,,616760,MONDO:0014765,"wooly hair, autosomal recessive 3",
+BMGC_DS15794,BMG_DS060119,,SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES,,,,,,,C4225215,,610876;616756,MONDO:0014764,spastic paraplegia-severe developmental delay-epilepsy syndrome,
+BMGC_DS15795,BMG_DS060120,,"HETEROTAXY, VISCERAL, 7, AUTOSOMAL",,,,,,,C4225217,,616749;608416,MONDO:0014762,"heterotaxy, visceral, 7, autosomal",
+BMGC_DS15796,BMG_DS060121,,"AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE 1",,,,,DOID:0080944,familial Behcet-like autoinflammatory syndrome,C4225218,,616744;191163,MONDO:0800045,"autoinflammatory syndrome, familial, Behcet-like 1",
+BMGC_DS15797,BMG_DS060122,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 51",,,,,DOID:0081214,autosomal recessive intellectual developmental disorder 51,C4225220,,605238;616739,MONDO:0014759,"intellectual disability, autosomal recessive 51",
+BMGC_DS15798,BMG_DS060123,,RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2,,,,,,,C4225221,,616738,MONDO:0014758,radioulnar synostosis with amegakaryocytic thrombocytopenia 2,
+BMGC_DS15799,BMG_DS060124,1172685001,"Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome",,,,,,,C4225222,,616737,MONDO:0014757,macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome,"Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome | Macrothrombocytopenia, lymphoedema, developmental delay, facial dysmorphism, camptodactyly syndrome | Takenouchi Kosaki syndrome | Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome (disorder)"
+BMGC_DS15800,BMG_DS060125,,"TREMOR, HEREDITARY ESSENTIAL, 5",,,,,DOID:0111432,essential tremor 5,C4225223,,610084;616736,MONDO:0014756,"tremor, hereditary essential, 5",
+BMGC_DS15801,BMG_DS060126,,,,,,,,,C4225225,,616734,MONDO:0014755,"skin creases, congenital symmetric circumferential, 2",
+BMGC_DS15802,BMG_DS060127,,"COENZYME Q10 DEFICIENCY, PRIMARY, 8",,,,,DOID:0070245,primary coenzyme Q10 deficiency 8,C4225226,,601683;616733,MONDO:0014754,primary coenzyme Q10 deficiency 8,
+BMGC_DS15803,BMG_DS060128,,"OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES",,,,,DOID:0111434,optic atrophy 10,C4225227,,616732,MONDO:0020737,"optic atrophy 10 with or without ataxia, intellectual disability, and seizures",
+BMGC_DS15804,BMG_DS060129,,"NEPHROTIC SYNDROME, TYPE 11",,,,,DOID:0080385,nephrotic syndrome type 11,C4225228,,616730;607617,MONDO:0014752,"nephrotic syndrome, type 11",
+BMGC_DS15805,BMG_DS060130,,"CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES",,,,,,,C4225229,,609132;616728,MONDO:0014751,palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome,
+BMGC_DS15806,BMG_DS060131,,"CILIARY DYSKINESIA, PRIMARY, 33",,,,,,,C4225230,,616726;605178,MONDO:0014750,primary ciliary dyskinesia 33,
+BMGC_DS15807,BMG_DS060132,,"TOOTH AGENESIS, SELECTIVE, 7",,,,,,,C4225231,,616724;603507,MONDO:0014749,"tooth agenesis, selective, 7",
+BMGC_DS15808,BMG_DS060133,1187171005,SLC39A8 congenital disorder of glycosylation,,,,,,,C4225234,,616721,MONDO:0014746,SLC39A8-CDG,Solute carrier family 39 member 8 congenital disorder of glycosylation | SLC39A8-CDG - solute carrier family 39 member 8 congenital disorder of glycosylation | Congenital disorder of glycosylation type 2n | SLC39A8 congenital disorder of glycosylation | Congenital disorder of glycosylation type IIn | Carbohydrate deficient glycoprotein syndrome type IIn | Solute carrier family 39 member 8 congenital disorder of glycosylation (disorder)
+BMGC_DS15809,BMG_DS060134,,"MYASTHENIC SYNDROME, CONGENITAL, 19",,,,,DOID:0110673,congenital myasthenic syndrome 19,C4225235,,616720;120350,MONDO:0014745,congenital myasthenic syndrome 19,
+BMGC_DS15810,BMG_DS060135,,,,,,,,,C4225237,,616716,MONDO:0014743,rhizomelic chondrodysplasia punctata type 5,
+BMGC_DS15811,BMG_DS060136,,"PARKINSON DISEASE 22, AUTOSOMAL DOMINANT",,,,,DOID:0080504,Parkinson's disease 22,C4225238,,616710;616244,MONDO:0014742,"Parkinson disease 22, autosomal dominant",
+BMGC_DS15812,BMG_DS060137,,DESANTO-SHINAWI SYNDROME,,,,,DOID:0081126,DeSanto-Shinawi syndrome,C4225239,,616708;615049,MONDO:0018760,DeSanto-Shinawi syndrome,
+BMGC_DS15813,BMG_DS060138,,"DEAFNESS, AUTOSOMAL DOMINANT 68",,,,,,,C4225240,,604799;616707,MONDO:0014740,autosomal dominant nonsyndromic hearing loss 68,
+BMGC_DS15814,BMG_DS060139,,"DEAFNESS, AUTOSOMAL DOMINANT 69",,,,,,,C4225241,,616697;184745,MONDO:0014738,autosomal dominant nonsyndromic hearing loss 69,
+BMGC_DS15815,BMG_DS060140,,DEHYDRATED HEREDITARY STOMATOCYTOSIS 2,,,,,DOID:0111577,dehydrated hereditary stomatocytosis 2,C4225242,,616689;602754,MONDO:0014737,dehydrated hereditary stomatocytosis 2,
+BMGC_DS15816,BMG_DS060141,,,,,,,,,C4225245,,616685,MONDO:0014734,"epilepsy, idiopathic generalized, susceptibility to, 14",
+BMGC_DS15817,BMG_DS060142,765047006,SURF1-related Charcot-Marie-Tooth disease type 4,,,,,,,C4225246,,616684,MONDO:0014733,Charcot-Marie-Tooth disease type 4K,"SURF1, cytochrome c oxidase assembly factor related Charcot-Marie-Tooth disease type 4 (disorder) | Charcot-Marie-Tooth disease type 4K | SURF1-related Charcot-Marie-Tooth disease type 4 | SURF1-related severe demyelinating Charcot-Marie-Tooth disease | SURF1, cytochrome c oxidase assembly factor related Charcot-Marie-Tooth disease type 4"
+BMGC_DS15818,BMG_DS060143,,"LEUKODYSTROPHY, HYPOMYELINATING, 12",,,,,DOID:0060796,hypomyelinating leukodystrophy 12,C4225247,,616683;608549,MONDO:0014732,hypomyelinating leukodystrophy 12,
+BMGC_DS15819,BMG_DS060144,1187250005,"Seizures, scoliosis, macrocephaly syndrome",,,,,,,C4225248,,616682,MONDO:0014731,seizures-scoliosis-macrocephaly syndrome,"SSM (seizures, scoliosis, macrocephaly) syndrome | Seizures, scoliosis, macrocephaly syndrome (disorder) | Seizures, scoliosis, macrocephaly syndrome"
+BMGC_DS15820,BMG_DS060145,,"MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE",,,,,DOID:0070289,primary autosomal recessive microcephaly 16,C4225249,,616681;616062,MONDO:0014730,"microcephaly 16, primary, autosomal recessive",
+BMGC_DS15821,BMG_DS060146,,"SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE",,,,,,,C4225250,,159460;616680,MONDO:0014729,hereditary spastic paraplegia 75,
+BMGC_DS15822,BMG_DS060147,,IMMUNODEFICIENCY 45,,,,,DOID:0111994,immunodeficiency 45,C4225252,,616669;602376,MONDO:0014727,immunodeficiency 45,
+BMGC_DS15823,BMG_DS060148,1237418002,"Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome",,,,,DOID:0070537,"spastic tetraplegia, thin corpus callosum, and progressive microcephaly",C4225254,,616657,MONDO:0014725,spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome,"Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome | ASCT1 deficiency | Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome (disorder) | Spastic quadriplegia, thin corpus callosum, progressive postnatal microcephaly syndrome"
+BMGC_DS15824,BMG_DS060149,1172899000,PMP22-RAI1 contiguous gene duplication syndrome,,,,,,,C4225255,,616652,MONDO:0014723,PMP22-RAI1 contiguous gene duplication syndrome,Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome (disorder) | PMP22-RAI1 contiguous gene duplication syndrome | 17p11.2p12 microduplication syndrome | Yuan Harel Lupski syndrome | Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome | Trisomy 17p11.2p12
+BMGC_DS15825,BMG_DS060150,1208747005,ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement,,,,,,,C4225256,,616647,MONDO:0014719,"developmental and epileptic encephalopathy, 35",Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement | ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement | Martsolf-like syndrome | Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement (disorder)
+BMGC_DS15826,BMG_DS060151,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 34,,,,,DOID:0080460,developmental and epileptic encephalopathy 34,C4225257,,616645;606726,MONDO:0014718,"developmental and epileptic encephalopathy, 34",
+BMGC_DS15827,BMG_DS060152,,"EPILEPSY, PROGRESSIVE MYOCLONIC, 10",,,,,DOID:0111445,progressive myoclonus epilepsy 10,C4225258,,616640;616639,MONDO:0014717,early-onset Lafora body disease,
+BMGC_DS15828,BMG_DS060153,1187304005,"Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome",,,,,,,C4225259,,616638,MONDO:0014716,macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome,"MINDS syndrome | Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome (disorder) | Smith Kingsmore syndrome | MINDS (macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax) syndrome"
+BMGC_DS15829,BMG_DS060154,,IMMUNODEFICIENCY 44,,,,,DOID:0111975,immunodeficiency 44,C4225260,,616636;600556,MONDO:0014715,primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection,
+BMGC_DS15830,BMG_DS060155,,"POROKERATOSIS 9, MULTIPLE TYPES",,,,,,,C4225262,,616631;134629,MONDO:0014713,"porokeratosis 9, multiple types",
+BMGC_DS15831,BMG_DS060156,,SENIOR-LOKEN SYNDROME 9,,,,,,,C4225263,,607380;616629,MONDO:0014712,Senior-Loken syndrome 9,
+BMGC_DS15832,BMG_DS060157,,HEIMLER SYNDROME 2,,,,,DOID:0080624,Heimler syndrome 2,C4225267,,616617;601498,,,
+BMGC_DS15833,BMG_DS060158,,"CUTIS LAXA, AUTOSOMAL DOMINANT 3",,,,,,,C4225268,,616603;138250,MONDO:0014706,"cutis laxa, autosomal dominant 3",
+BMGC_DS15834,BMG_DS060159,,CRANIOSYNOSTOSIS 6,,,,,DOID:0061008,craniosynostosis 6,C4225269,,616602;600470,MONDO:0014705,craniosynostosis 6,
+BMGC_DS15835,BMG_DS060160,1172898008,Kosaki overgrowth syndrome,,,,,,,C4225270,,616592,MONDO:0014704,skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome,"Kosaki overgrowth syndrome (disorder) | Skeletal overgrowth, craniofacial dysmorphism, hyperelastic skin, white matter lesion syndrome | Kosaki overgrowth syndrome"
+BMGC_DS15836,BMG_DS060161,,ADAMS-OLIVER SYNDROME 6,,,,,,,C4225271,,616589;605185,MONDO:0014703,Adams-Oliver syndrome 6,
+BMGC_DS15837,BMG_DS060162,1228860003,Spondyloepiphyseal dysplasia Stanescu type,,,,,,,C4225273,,616583,MONDO:0014701,"spondyloepiphyseal dysplasia, Stanescu type",Spondyloepiphyseal dysplasia Stanescu type | Spondyloepiphyseal dysplasia Stanescu type (disorder) | SED (spondyloepiphyseal dysplasia) Stanescu type
+BMGC_DS15838,BMG_DS060163,,,,,,,,,C4225274,,616580;604916,MONDO:0014700,Au-Kline syndrome,
+BMGC_DS15839,BMG_DS060164,1254651003,"Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome",,,,,,,C4225276,,616577,MONDO:0014698,microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome,"Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (disorder) | Microcephaly, intellectual disability, sensorineural deafness, epilepsy, abnormal muscle tone syndrome | Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome"
+BMGC_DS15840,BMG_DS060165,,"IMMUNODEFICIENCY, COMMON VARIABLE, 12, WITH AUTOIMMUNITY",,,,,DOID:0081154,common variable immunodeficiency 12,C4225277,,616576;164011,MONDO:0014697,"immunodeficiency, common variable, 12",
+BMGC_DS15841,BMG_DS060166,,"SPONDYLOCOSTAL DYSOSTOSIS 6, AUTOSOMAL RECESSIVE",,,,,DOID:0112360,spondylocostal dysostosis 6,C4225279,,616566;609891,MONDO:0014694,"spondylocostal dysostosis 6, autosomal recessive",
+BMGC_DS15842,BMG_DS060167,,NOONAN SYNDROME 10,,,,,,,C4225280,,616564;600574,MONDO:0014693,Noonan syndrome 10,
+BMGC_DS15843,BMG_DS060168,,RETINITIS PIGMENTOSA 74,,,,,,,C4225281,,616562;606151,MONDO:0014692,retinitis pigmentosa 74,
+BMGC_DS15844,BMG_DS060169,,NOONAN SYNDROME 9,,,,,,,C4225282,,616559;601247,MONDO:0014691,Noonan syndrome 9,
+BMGC_DS15845,BMG_DS060170,,"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 7",,,,,DOID:0070023,autosomal dominant dyskeratosis congenita 6,C4225283,,609377;616553,MONDO:0800370,"dyskeratosis congenita, autosomal recessive 7",
+BMGC_DS15846,BMG_DS060171,,"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6",,,,,DOID:0070023,autosomal dominant dyskeratosis congenita 6,C4225284,,616553;609377,MONDO:0014690,"dyskeratosis congenita, autosomal dominant 6",
+BMGC_DS15847,BMG_DS060172,1217225001,"Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome",,,,,,,C4225285,,616549,MONDO:0014689,Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome,"Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome | Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome (disorder)"
+BMGC_DS15848,BMG_DS060173,,SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY,,,,,,,C4225286,,610178;616546,MONDO:0014688,short-rib thoracic dysplasia 14 with polydactyly,
+BMGC_DS15849,BMG_DS060174,,RETINITIS PIGMENTOSA 73,,,,,,,C4225287,,610453;616544,MONDO:0014687,retinitis pigmentosa 73,
+BMGC_DS15850,BMG_DS060175,,"SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION",,,,,,,C4225288,,194363;616541,MONDO:0014686,"short stature, microcephaly, and endocrine dysfunction",
+BMGC_DS15851,BMG_DS060176,1228857005,Progressive myoclonic epilepsy type 9,,,,,,,C4225289,,616540,MONDO:0014685,progressive myoclonic epilepsy type 9,Progressive myoclonic epilepsy type 9 | Progressive myoclonic epilepsy type 9 (disorder) | Progressive myoclonic epilepsy due to LMNB2 deficiency | Progressive myoclonic epilepsy due to LMNB2 (lamin B2) deficiency | Progressive myoclonus epilepsy type 9 | PME (progressive myoclonic epilepsy) type 9
+BMGC_DS15852,BMG_DS060177,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9",,,,,DOID:0111232,congenital muscular dystrophy-dystroglycanopathy type A9,C4225291,,128239;616538,MONDO:0014683,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9",
+BMGC_DS15853,BMG_DS060178,,,,,,,,,C4225292,,616535,MONDO:0014682,"thyroid cancer, nonmedullary, 5",
+BMGC_DS15854,BMG_DS060179,,,,,,,,,C4225293,,616534,MONDO:0014681,"thyroid cancer, nonmedullary, 4",
+BMGC_DS15855,BMG_DS060180,,,,,,,,,C4225294,,616532,MONDO:0014680,"herpes simplex encephalitis, susceptibility to, 7",
+BMGC_DS15856,BMG_DS060181,,"NEURODEVELOPMENTAL DISORDER WITH SPASTICITY, HYPOMYELINATING LEUKODYSTROPHY, AND BRAIN ABNORMALITIES",,,,,,,C4225295,,616531;600286,MONDO:0014679,"polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis",
+BMGC_DS15857,BMG_DS060182,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 39",,,,,DOID:0070069,autosomal dominant intellectual developmental disorder 39,C4225296,,613084;616521,MONDO:0014678,"intellectual disability, autosomal dominant 39",
+BMGC_DS15858,BMG_DS060183,,ACHROMATOPSIA 7,,,,,DOID:0110009,achromatopsia 7,C4225297,,605537;616517,MONDO:0014677,achromatopsia 7,
+BMGC_DS15859,BMG_DS060184,,"DEAFNESS, AUTOSOMAL RECESSIVE 104",,,,,,,C4225298,,616515;611410,MONDO:0014675,autosomal recessive nonsyndromic hearing loss 104,
+BMGC_DS15860,BMG_DS060185,,"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 14",,,,,DOID:0111111,maturity-onset diabetes of the young type 14,C4225299,,604299;616511,MONDO:0014674,maturity-onset diabetes of the young type 14,
+BMGC_DS15861,BMG_DS060186,,CATARACT 44,,,,,,,C4225300,,600909;616509,MONDO:0014673,cataract 44,
+BMGC_DS15862,BMG_DS060187,,"OSTEOGENESIS IMPERFECTA, TYPE XVII",,,,,,,C4225301,,616507;182120,MONDO:0014672,osteogenesis imperfecta type 17,
+BMGC_DS15863,BMG_DS060188,,"NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB, WITH OPTIC ATROPHY",,,,,,,C4225302,,616505,MONDO:0014671,"neuropathy, hereditary motor and sensory, type 6B",
+BMGC_DS15864,BMG_DS060189,,LETHAL CONGENITAL CONTRACTURE SYNDROME 9,,,,,,,C4225303,,616503;612243,MONDO:0014670,lethal congenital contracture syndrome 9,
+BMGC_DS15865,BMG_DS060190,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 13",,,,,DOID:0080360,mitochondrial complex IV deficiency nuclear type 13,C4225304,,616501;614772,MONDO:0014668,"cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4",
+BMGC_DS15866,BMG_DS060191,,"LEUKODYSTROPHY, HYPOMYELINATING, 11",,,,,,,C4225305,,616494;610060,MONDO:0014666,hypomyelinating leukodystrophy 11,
+BMGC_DS15867,BMG_DS060192,,SILVER-RUSSELL SYNDROME 3,,,,,,,C4225307,,616489;147470,MONDO:0014663,Silver-Russell syndrome 3,
+BMGC_DS15868,BMG_DS060193,1172838005,Hereditary sensory and autonomic neuropathy type 8,,,,,,,C4225308,,616488,MONDO:0014662,congenital insensitivity to pain-hypohidrosis syndrome,Hereditary sensory and autonomic neuropathy type 8 (disorder) | HSAN8 - hereditary sensory and autonomic neuropathy type 8 | Hereditary sensory and autonomic neuropathy type 8 | Hereditary sensory and autonomic neuropathy type VIII
+BMGC_DS15869,BMG_DS060194,,"EPIDERMOLYSIS BULLOSA SIMPLEX 5D, GENERALIZED INTERMEDIATE, AUTOSOMAL RECESSIVE",,,,,,,C4225309,,616487;601282,MONDO:0014661,epidermolysis bullosa simplex with nail dystrophy,
+BMGC_DS15870,BMG_DS060195,,"NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN IMAGING ABNORMALITIES",,,,,DOID:0070277,primary autosomal recessive microcephaly 15,C4225310,,616486;614397,MONDO:0014660,"microcephaly 15, primary, autosomal recessive",
+BMGC_DS15871,BMG_DS060196,,"CILIARY DYSKINESIA, PRIMARY, 32",,,,,,,C4225311,,616481;615876,MONDO:0014657,primary ciliary dyskinesia 32,
+BMGC_DS15872,BMG_DS060197,,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2",,,,,DOID:0111515,autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2,C4225312,,616479;604123,MONDO:0014656,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2",
+BMGC_DS15873,BMG_DS060198,,BETHLEM MYOPATHY 2,,,,,,,C4225313,,120320;616471,MONDO:0034022,Bethlem myopathy 2,
+BMGC_DS15874,BMG_DS060199,,ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2,,,,,DOID:0060948,Ullrich congenital muscular dystrophy 2,C4225314,,120320;616470,MONDO:0014654,Ullrich congenital muscular dystrophy 2,
+BMGC_DS15875,BMG_DS060200,,RETINITIS PIGMENTOSA 72,,,,,,,C4225315,,616454;616469,MONDO:0014653,retinitis pigmentosa 72,
+BMGC_DS15876,BMG_DS060201,,EXUDATIVE VITREORETINOPATHY 6,,,,,DOID:0111410,exudative vitreoretinopathy 6,C4225316,,616468;616454,MONDO:0014652,exudative vitreoretinopathy 6,
+BMGC_DS15877,BMG_DS060202,,"ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE",,,,,DOID:0060353,acrofacial dysostosis Cincinnati type,C4225317,,616462;616404,MONDO:0014651,acrofacial dysostosis Cincinnati type,
+BMGC_DS15878,BMG_DS060203,,"EPILEPSY, FAMILIAL TEMPORAL LOBE, 8",,,,,DOID:0060754,familial temporal lobe epilepsy 8,C4225318,,616461;137035,MONDO:0014650,familial temporal lobe epilepsy 8,
+BMGC_DS15879,BMG_DS060204,,,,,,,,,C4225319,,616460,MONDO:0014649,"intellectual disability, autosomal recessive 50",
+BMGC_DS15880,BMG_DS060205,1237417007,"CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation",,,,,,,C4225320,,616457,MONDO:0014647,"developmental and epileptic encephalopathy, 50","Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation | Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation (disorder) | CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation | Carbohydrate deficient glycoprotein syndrome type Iz | Congenital disorder of glycosylation type 1z"
+BMGC_DS15881,BMG_DS060206,,ZIMMERMANN-LABAND SYNDROME 2,,,,,,,C4225321,,616455;606939,MONDO:0014646,Zimmermann-Laband syndrome 2,
+BMGC_DS15882,BMG_DS060207,1187644009,Basel Vanagaite Smirin Yosef syndrome,,,,,,,C4225323,,616449,MONDO:0014643,congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome,Basel Vanagaite Smirin Yosef syndrome (disorder) | Basel Vanagaite Smirin Yosef syndrome
+BMGC_DS15883,BMG_DS060208,,"CANDIDIASIS, FAMILIAL, 9",,,,,,,C4225324,,610925;616445,MONDO:0014642,"candidiasis, familial, 9",
+BMGC_DS15884,BMG_DS060209,,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4,,,,,DOID:0110069,frontotemporal dementia and/or amyotrophic lateral sclerosis 4,C4225325,,616439;604834,MONDO:0014641,frontotemporal dementia and/or amyotrophic lateral sclerosis 4,
+BMGC_DS15885,BMG_DS060210,,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3,,,,,DOID:0110068,frontotemporal dementia and/or amyotrophic lateral sclerosis 3,C4225326,,616437;601530,MONDO:0014640,frontotemporal dementia and/or amyotrophic lateral sclerosis 3,
+BMGC_DS15886,BMG_DS060211,,"EPILEPSY, FAMILIAL TEMPORAL LOBE, 7",,,,,DOID:0060751,familial temporal lobe epilepsy 7,C4225327,,616436;600514,MONDO:0014639,familial temporal lobe epilepsy 7,
+BMGC_DS15887,BMG_DS060212,,IMMUNODEFICIENCY 40,,,,,DOID:0111951,immunodeficiency 40,C4225328,,603122;616433,MONDO:0014637,DOCK2 deficiency,
+BMGC_DS15888,BMG_DS060213,,,,,,,,,C4225330,,616428,MONDO:0014635,"microphthalmia, isolated, with coloboma 10",
+BMGC_DS15889,BMG_DS060214,,"46,XY SEX REVERSAL 10",,,,,DOID:0111775,"46,XY sex reversal 10",C4225331,,608160;616425,MONDO:0014634,"46,XY sex reversal 10",
+BMGC_DS15890,BMG_DS060215,1237421000,"PYCR2-related microcephaly, progressive leukoencephalopathy",,,,,,,C4225332,,616420,MONDO:0014632,hypomyelinating leukodystrophy 10,"Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leucoencephalopathy | PYCR2-related microcephaly, progressive leucoencephalopathy | Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leukoencephalopathy (disorder) | Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leukoencephalopathy | PYCR2-related microcephaly, progressive leukoencephalopathy"
+BMGC_DS15891,BMG_DS060216,,"HYPOMAGNESEMIA, SEIZURES, AND IMPAIRED INTELLECTUAL DEVELOPMENT 1",,,,,,,C4225333,,607803;616418,MONDO:0020787,"hypomagnesemia, seizures, and intellectual disability 1",
+BMGC_DS15892,BMG_DS060217,,"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6",,,,,,,C4225335,,605237;616413,MONDO:0014628,"basal ganglia calcification, idiopathic, 6",
+BMGC_DS15893,BMG_DS060218,,DYSTONIA 27,,,,,,,C4225336,,120250;616411,MONDO:0014627,dystonia 27,
+BMGC_DS15894,BMG_DS060219,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 33,,,,,DOID:0080463,developmental and epileptic encephalopathy 33,C4225337,,602959;616409,MONDO:0014625,"developmental and epileptic encephalopathy, 33",
+BMGC_DS15895,BMG_DS060220,,"MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE",,,,,DOID:0070279,primary autosomal recessive microcephaly 14,C4225338,,609321;616402,MONDO:0014623,"microcephaly 14, primary, autosomal recessive",
+BMGC_DS15896,BMG_DS060221,,"PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 2",,,,,DOID:0111711,focal nonepidermolytic palmoplantar keratoderma 2,C4225339,,616400;607066,MONDO:0014622,isolated focal non-epidermolytic palmoplantar keratoderma,
+BMGC_DS15897,BMG_DS060222,,BRUGADA SYNDROME 9,,,,,,,C4225340,,616399;605411,MONDO:0014621,Brugada syndrome 9,
+BMGC_DS15898,BMG_DS060223,,"DYSTONIA 26, MYOCLONIC",,,,,DOID:0090036,myoclonic dystonia 26,C4225341,,616398;616386,MONDO:0014620,myoclonic dystonia 26,
+BMGC_DS15899,BMG_DS060224,,RETINITIS PIGMENTOSA 71,,,,,,,C4225342,,616394;607386,MONDO:0014618,retinitis pigmentosa 71,
+BMGC_DS15900,BMG_DS060225,,,,,,,,,C4225343,,616393,MONDO:0014617,"intellectual disability, autosomal dominant 38",
+BMGC_DS15901,BMG_DS060226,,"TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE",,,,,DOID:0111869,photosensitive trichothiodystrophy 2,C4225344,,616390;133510,MONDO:0014615,"trichothiodystrophy 2, photosensitive",
+BMGC_DS15902,BMG_DS060227,,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G",,,,,DOID:0110714,congenital stationary night blindness 1G,C4225345,,616389;139330,MONDO:0014614,congenital stationary night blindness 1G,
+BMGC_DS15903,BMG_DS060228,,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 3",,,,,,,C4225346,,616373;608833,MONDO:0014613,"pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3",
+BMGC_DS15904,BMG_DS060229,,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 4",,,,,,,C4225347,,616371;604212,MONDO:0014612,"pulmonary fibrosis and/or bone marrow failure, Telomere-related, 4",
+BMGC_DS15905,BMG_DS060230,1208621008,Multiple mitochondrial dysfunctions syndrome type 4,,,,,,,C4225348,,616370,MONDO:0014611,multiple mitochondrial dysfunctions syndrome 4,Multiple mitochondrial dysfunctions syndrome type 4 | MMDS4 - multiple mitochondrial dysfunctions syndrome type 4 | Multiple mitochondrial dysfunctions syndrome type 4 (disorder)
+BMGC_DS15906,BMG_DS060231,1216943004,Mandibulofacial dysostosis with alopecia,,,,,,,C4225349,,616367,MONDO:0014608,mandibulofacial dysostosis with alopecia,Mandibulofacial dysostosis with alopecia | MFDA - mandibulofacial dysostosis with alopecia | Mandibulofacial dysostosis with alopecia (disorder)
+BMGC_DS15907,BMG_DS060232,,,,,,,,,C4225350,,616366,MONDO:0014607,"developmental and epileptic encephalopathy, 32",
+BMGC_DS15908,BMG_DS060233,772127009,White Sutton syndrome,,,,,,,C4225351,,616364,MONDO:0014606,intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome,White Sutton syndrome (disorder) | White Sutton syndrome
+BMGC_DS15909,BMG_DS060234,1254650002,"Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome",,,,,,,C4225352,,616362,MONDO:0014605,Houge-Janssens syndrome 2,"Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome (disorder) | Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome"
+BMGC_DS15910,BMG_DS060235,,PARKINSON DISEASE 21,,,,,DOID:0111251,Parkinson's disease 21,C4225353,,616361,MONDO:0014604,Parkinson disease 21,
+BMGC_DS15911,BMG_DS060236,1254652005,"Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome",,,,,,,C4225354,,,,,"Intellectual disability, macrocephaly, hypotonia, behavioural abnormalities syndrome | Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome | Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome (disorder)"
+BMGC_DS15912,BMG_DS060237,,"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6",,,,,DOID:0070024,autosomal recessive dyskeratosis congenita 6,C4225356,,616353;604212,MONDO:0014600,"dyskeratosis congenita, autosomal recessive 6",
+BMGC_DS15913,BMG_DS060238,,,,,,,,,C4225357,,616346,MONDO:0014598,"developmental and epileptic encephalopathy, 31A",
+BMGC_DS15914,BMG_DS060239,,IMMUNODEFICIENCY 39,,,,,DOID:0111969,immunodeficiency 39,C4225358,,605047;616345,MONDO:0014597,immunodeficiency 39,
+BMGC_DS15915,BMG_DS060240,,LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA,,,,,DOID:0112231,lissencephaly 7 with cerebellar hypoplasia,C4225359,,123831;616342,MONDO:0014596,lissencephaly 7 with cerebellar hypoplasia,
+BMGC_DS15916,BMG_DS060241,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 30,,,,,DOID:0080465,developmental and epileptic encephalopathy 30,C4225360,,605705;616341,MONDO:0014595,"developmental and epileptic encephalopathy, 30",
+BMGC_DS15917,BMG_DS060242,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 29,,,,,DOID:0080451,developmental and epileptic encephalopathy 29,C4225361,,601065;616339,MONDO:0014593,"developmental and epileptic encephalopathy, 29",
+BMGC_DS15918,BMG_DS060243,,"MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3",,,,,DOID:0080107,microcephaly and chorioretinopathy 3,C4225362,,609610;616335,MONDO:0014592,microcephaly and chorioretinopathy 3,
+BMGC_DS15919,BMG_DS060244,,"ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2",,,,,DOID:0060765,autosomal dominant Robinow syndrome 2,C4225363,,601365;616331,MONDO:0014591,autosomal dominant Robinow syndrome 2,
+BMGC_DS15920,BMG_DS060245,,"MYASTHENIC SYNDROME, CONGENITAL, 18",,,,,DOID:0110683,congenital myasthenic syndrome 18,C4225364,,616330,MONDO:0014590,congenital myasthenic syndrome 18,
+BMGC_DS15921,BMG_DS060246,,"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13",,,,,DOID:0111110,maturity-onset diabetes of the young type 13,C4225365,,600937;616329,MONDO:0014589,maturity-onset diabetes of the young type 13,
+BMGC_DS15922,BMG_DS060247,,"MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY",,,,,DOID:0110675,congenital myasthenic syndrome 11,C4225367,,616326;601592,MONDO:0014588,congenital myasthenic syndrome 11,
+BMGC_DS15923,BMG_DS060248,,"MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY",,,,,DOID:0110670,congenital myasthenic syndrome 9,C4225368,,616325;601296,MONDO:0014587,congenital myasthenic syndrome 9,
+BMGC_DS15924,BMG_DS060249,,"MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL",,,,,DOID:0110677,congenital myasthenic syndrome 4B,C4225369,,616324;100725,MONDO:0014586,congenital myasthenic syndrome 4B,
+BMGC_DS15925,BMG_DS060250,,"MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY",,,,,DOID:0110664,congenital myasthenic syndrome 3C,C4225370,,616323;100720,MONDO:0014585,congenital myasthenic syndrome 3C,
+BMGC_DS15926,BMG_DS060251,,"MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL",,,,,DOID:0110665,congenital myasthenic syndrome 3B,C4225371,,616322;100720,MONDO:0014584,congenital myasthenic syndrome 3B,
+BMGC_DS15927,BMG_DS060252,,"MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL",,,,,DOID:0110666,congenital myasthenic syndrome 3A,C4225372,,616321;100720,MONDO:0014583,congenital myasthenic syndrome 3A,
+BMGC_DS15928,BMG_DS060253,,"MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY",,,,,DOID:0110680,congenital myasthenic syndrome 2C,C4225373,,616314;100710,MONDO:0014582,congenital myasthenic syndrome 2C,
+BMGC_DS15929,BMG_DS060254,,"MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL",,,,,DOID:0110681,congenital myasthenic syndrome 2A,C4225374,,616313;100710,MONDO:0014581,congenital myasthenic syndrome 2A,
+BMGC_DS15930,BMG_DS060255,,,,,,,,,C4225375,,616311,MONDO:0014580,"intellectual disability, autosomal dominant 33",
+BMGC_DS15931,BMG_DS060256,,SENIOR-LOKEN SYNDROME 8,,,,,,,C4225376,,616307;608151,MONDO:0014579,Senior-Loken syndrome 8,
+BMGC_DS15932,BMG_DS060257,,"MYASTHENIC SYNDROME, CONGENITAL, 17",,,,,DOID:0110674,congenital myasthenic syndrome 17,C4225377,,616304;604270,MONDO:0014578,congenital myasthenic syndrome 17,
+BMGC_DS15933,BMG_DS060258,,SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY,,,,,,,C4225378,,613446;616300,MONDO:0014577,short-rib thoracic dysplasia 13 with or without polydactyly,
+BMGC_DS15934,BMG_DS060259,,LIPOYLTRANSFERASE 1 DEFICIENCY,,,,,,,C4225379,,616299;610284,MONDO:0014576,lipoyl transferase 1 deficiency,
+BMGC_DS15935,BMG_DS060260,,SINGLETON-MERTEN SYNDROME 2,,,,,,,C4225380,,616298;609631,MONDO:0014575,Singleton-Merten syndrome 2,
+BMGC_DS15936,BMG_DS060261,1237509001,PLACK syndrome,,,,,DOID:0070526,PLACK syndrome,C4225381,,616295,MONDO:0014574,peeling skin-leukonuchia-acral punctate keratoses-cheilitis-knuckle pads syndrome,"Peeling skin, leukonychia, acral punctate keratoses, cheilitis, knuckle pads syndrome (disorder) | PLACK syndrome | PLACK (peeling skin, leukonychia, acral punctate keratoses, cheilitis, knuckle pads) syndrome | Peeling skin, leukonychia, acral punctate keratoses, cheilitis, knuckle pads syndrome | Peeling skin, leuconychia, acral punctate keratoses, cheilitis, knuckle pads syndrome"
+BMGC_DS15937,BMG_DS060262,,COLE-CARPENTER SYNDROME 2,,,,,,,C4225382,,616294;607186,MONDO:0014573,Cole-Carpenter syndrome 2,
+BMGC_DS15938,BMG_DS060263,1237413006,"Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome",,,,,,,C4225383,,616291,MONDO:0014572,Lichtenstein-Knorr syndrome,"Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome (disorder) | Lichtenstein Knorr syndrome | SCAR19 - spinocerebellar ataxia, autosomal recessive 19 | Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome | Progressive autosomal recessive ataxia, deafness syndrome"
+BMGC_DS15939,BMG_DS060264,,OPTIC ATROPHY 9,,,,,DOID:0111442,optic atrophy 9,C4225384,,616289,MONDO:0014571,optic atrophy 9,
+BMGC_DS15940,BMG_DS060265,,LETHAL CONGENITAL CONTRACTURE SYNDROME 8,,,,,,,C4225385,,616287;600294,MONDO:0014570,lethal congenital contracture syndrome 8,
+BMGC_DS15941,BMG_DS060266,,LETHAL CONGENITAL CONTRACTURE SYNDROME 7,,,,,,,C4225386,,602346;616286,MONDO:0014569,lethal congenital contracture syndrome 7,
+BMGC_DS15942,BMG_DS060267,,NEURODEVELOPMENTAL DISORDER WITH SPASTIC PARAPLEGIA AND MICROCEPHALY,,,,,DOID:0070542,neurodevelopmental disorder with spastic paraplegia and microcephaly,C4225388,,138210;616281,MONDO:0014567,glutamate pyruvate transaminase 2 deficiency,
+BMGC_DS15943,BMG_DS060268,,CATARACT 43,,,,,,,C4225389,,616279;611220,MONDO:0014565,cataract 43,
+BMGC_DS15944,BMG_DS060269,,,,,,,,,C4225390,,616278,MONDO:0014564,congenital bile acid synthesis defect 5,
+BMGC_DS15945,BMG_DS060270,,MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY,,,,,DOID:0070540,mitochondrial short-chain enoyl-CoA hydratase 1 deficiency,C4225391,,616277;602292,MONDO:0014563,mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency,
+BMGC_DS15946,BMG_DS060271,764860006,3-methylglutaconic aciduria type 7,,,,,,,C4225393,,,,,"MGA7 - 3-methylglutaconic aciduria type 7 | 3-methylglutaconic aciduria type VII | 3-methylglutaconic aciduria type 7 (disorder) | 3-methylglutaconic aciduria type 7 | 3-methylglutaconic aciduria, cataract, neurologic involvement, neutropenia syndrome | CLBP (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency"
+BMGC_DS15947,BMG_DS060272,,"AMELOGENESIS IMPERFECTA, TYPE IF",,,,,,,C4225394,,616270;601259,MONDO:0014560,amelogenesis imperfecta type 1F,
+BMGC_DS15948,BMG_DS060273,1260130005,"Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome",,,,,,,C4225395,,616269,MONDO:0014559,progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome,"Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome | Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome (disorder) | Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behaviour syndrome"
+BMGC_DS15949,BMG_DS060274,1255319004,"Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome",,,,,,,C4225396,,616268,MONDO:0014558,autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome,"Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome | Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome (disorder) | Arboleda Tham syndrome"
+BMGC_DS15950,BMG_DS060275,,ATAXIA-OCULOMOTOR APRAXIA 4,,,,,DOID:0081383,ataxia-oculomotor apraxia type 4,C4225397,,616267;605610,MONDO:0014557,ataxia - oculomotor apraxia type 4,
+BMGC_DS15951,BMG_DS060276,1255322002,"Congenital contracture of limbs and face, hypotonia, developmental delay syndrome",,,,,,,C4225398,,616266,MONDO:0014556,"congenital contractures of the limbs and face, hypotonia, and developmental delay","Congenital contracture of limbs and face, hypotonia, developmental delay syndrome | CLIFAHDD syndrome | Congenital contracture of limbs and face, hypotonia, developmental delay syndrome (disorder) | CLIFAHDD (congenital limbs, face contractures, hypotonia, developmental delay) syndrome"
+BMGC_DS15952,BMG_DS060277,,SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES,,,,,,,C4225399,,108961;616255,MONDO:0014551,short stature with nonspecific skeletal abnormalities,
+BMGC_DS15953,BMG_DS060278,1228876007,Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency,,,,,,,C4225400,,615486,MONDO:0014206,severe early-onset pulmonary alveolar proteinosis due to MARS deficiency,Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency (disorder) | Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency | Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency | Interstitial lung and liver disease | Hereditary pulmonary alveolar proteinosis with hepatic involvement | Pulmonary alveolar proteinosis Reunion island type
+BMGC_DS15954,BMG_DS060279,,PREMATURE OVARIAN FAILURE 10,,,,,DOID:0080867,primary ovarian insufficiency 10,C4225402,,612885;608187,MONDO:0044776,premature ovarian failure 10,
+BMGC_DS15955,BMG_DS060280,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 23, WITH OR WITHOUT VENTRICULAR NONCOMPACTION",,,,,,,C4225403,,612158,,,
+BMGC_DS15956,BMG_DS060281,,"ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE",,,,,DOID:0081237,acromesomelic dysplasia-3,C4225404,,609441,MONDO:0012274,acromesomelic dysplasia 3,
+BMGC_DS15957,BMG_DS060282,,"MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL",,,,,DOID:0110662,congenital myasthenic syndrome 1B,C4225405,,608930;100690,MONDO:0012156,"myasthenic syndrome, congenital, 1B, fast-channel",
+BMGC_DS15958,BMG_DS060283,,PEELING SKIN SYNDROME 4,,,,,,,C4225407,,607936;184600,MONDO:0011937,peeling skin syndrome 4,
+BMGC_DS15959,BMG_DS060284,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25",,,,,DOID:0110328,hypertrophic cardiomyopathy 25,C4225408,,607487;604488,MONDO:0011843,hypertrophic cardiomyopathy 25,
+BMGC_DS15960,BMG_DS060285,,,,,,,,,C4225410,,606240,MONDO:0011653,"thyroid cancer, nonmedullary, 3",
+BMGC_DS15961,BMG_DS060286,,DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS,,,,,DOID:0111894,Diamond-Blackfan anemia 15 with mandibulofacial dysostosis,C4225411,,606164;603685,MONDO:0011639,Diamond-Blackfan anemia 15 with mandibulofacial dysostosis,
+BMGC_DS15962,BMG_DS060287,715653007,Spondylo-ocular syndrome,,,,,,,C4225412,,605822,MONDO:0011604,spondylo-ocular syndrome,Spondyloocular syndrome (disorder) | Spondyloocular syndrome | Spondylo-ocular syndrome
+BMGC_DS15963,BMG_DS060288,,"MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL",,,,,DOID:0110678,congenital myasthenic syndrome 4A,C4225413,,100725;605809,MONDO:0011600,congenital myasthenic syndrome 4A,
+BMGC_DS15964,BMG_DS060289,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 24",,,,,,,C4225414,,601493;605906,,,
+BMGC_DS15965,BMG_DS060290,,"MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3",,,,,DOID:0111184,"myopathy, lactic acidosis, and sideroblastic anemia 3",C4225415,,500011,MONDO:0010782,"myopathy, lactic acidosis, and sideroblastic anemia 3",
+BMGC_DS15966,BMG_DS060291,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED",,,,,DOID:0112025,female-restricted syndromic X-linked intellectual disability 99,C4225416,,300072;300968,MONDO:0010502,"intellectual disability, X-linked 99, syndromic, female-restricted",
+BMGC_DS15967,BMG_DS060292,,,,,,,,,C4225417,,300967,MONDO:0010501,syndromic X-linked intellectual disability 34,
+BMGC_DS15968,BMG_DS060293,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33",,,,,,,C4225418,,300966;313650,MONDO:0010500,"intellectual disability, X-linked, syndromic 33",
+BMGC_DS15969,BMG_DS060294,,RITSCHER-SCHINZEL SYNDROME 2,,,,,DOID:0060572,Ritscher-Schinzel syndrome 2,C4225419,,300859;300963,MONDO:0010499,Ritscher-Schinzel syndrome 2,
+BMGC_DS15970,BMG_DS060295,,"TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE",,,,,,,C4225420,,300951;300953,MONDO:0010495,"trichothiodystrophy 5, nonphotosensitive",
+BMGC_DS15971,BMG_DS060296,,LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3,,,,,DOID:0111876,linear skin defects with multiple congenital anomalies 3,C4225421,,300403;300952,MONDO:0010494,linear skin defects with multiple congenital anomalies 3,
+BMGC_DS15972,BMG_DS060297,,DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS,,,,,DOID:0111897,Diamond-Blackfan anemia 14 with mandibulofacial dysostosis,C4225422,,300946,MONDO:0010493,Diamond-Blackfan anemia 14 with mandibulofacial dysostosis,
+BMGC_DS15973,BMG_DS060298,,"REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET",,,,,DOID:0080090,reducing body myopathy 1A,C4225423,,300717,MONDO:0010414,"myopathy, reducing body, X-linked, early-onset, severe",
+BMGC_DS15974,BMG_DS060299,1197357008,"Colobomatous optic disc, macular atrophy, chorioretinopathy syndrome",,,,,,,C4225424,,212550,MONDO:0008927,colobomatous optic disc-macular atrophy-chorioretinopathy syndrome,"Colobomatous optic disc, macular atrophy, chorioretinopathy syndrome | Colobomatous optic disc, macular atrophy, chorioretinopathy syndrome (disorder)"
+BMGC_DS15975,BMG_DS060300,,"ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY",,,,,DOID:0060065,autosomal recessive pyridoxine-refractory sideroblastic anemia 2,C4225425,,205950;610819,MONDO:0008785,sideroblastic anemia 2,
+BMGC_DS15976,BMG_DS060301,,,,,,,,,C4225426,,188470,MONDO:0008566,"thyroid cancer, nonmedullary, 2",
+BMGC_DS15977,BMG_DS060302,,SINGLETON-MERTEN SYNDROME 1,,,,,,,C4225427,,182250;606951,MONDO:0024535,Singleton-Merten syndrome 1,
+BMGC_DS15978,BMG_DS060303,,"ANEMIA, SIDEROBLASTIC, 4",,,,,DOID:0060335,autosomal dominant sideroblastic anemia 4,C4225428,,182170;600548,MONDO:0008422,autosomal dominant sideroblastic anemia,
+BMGC_DS15979,BMG_DS060304,715318006,Ehlers-Danlos syndrome classic type,,,,,,,C4225429,,,MONDO:0007522,"Ehlers-Danlos syndrome, classic type",Ehlers-Danlos syndrome classic type (disorder) | Ehlers-Danlos syndrome classic type | Ehlers-Danlos syndrome classical type | Classical Ehlers-Danlos syndrome
+BMGC_DS15980,BMG_DS060305,,CHROMOSOME 10p12-p11 DELETION SYNDROME,,,,,DOID:0081126,DeSanto-Shinawi syndrome,C4225431,,616708,,,
+BMGC_DS15981,BMG_DS060306,,CHROMOSOME 2p25.3 DUPLICATION SYNDROME,,,,,DOID:0070069,autosomal dominant intellectual developmental disorder 39,C4225432,,616521,,,
+BMGC_DS15982,BMG_DS060307,,CHROMOSOME 2p25.3 DELETION SYNDROME,,,,,DOID:0070069,autosomal dominant intellectual developmental disorder 39,C4225433,,616521,,,
+BMGC_DS15983,BMG_DS060308,,"CHROMOSOME 5q14.3 DELETION SYNDROME, PROXIMAL",,,,,DOID:0070050,"neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language",C4225434,,613443,,,
+BMGC_DS15984,BMG_DS060309,,"RETINAL DYSTROPHY, EARLY-ONSET, WITH OR WITHOUT PITUITARY DYSFUNCTION",,,,,,,C4225436,,610125,,,
+BMGC_DS15985,BMG_DS060310,,"EPILEPSY, PROGRESSIVE MYOCLONIC, WITH SENSORY ATAXIC NEUROPATHY",,,,,,,C4225440,,607459,,,
+BMGC_DS15986,BMG_DS060311,,"PLASMINOGEN DEFICIENCY, TYPE II",,,,,,,C4225445,,217090,MONDO:0100538,dysplasminogenemia,
+BMGC_DS15987,BMG_DS060312,1234830005,14q32 duplication syndrome,,,,,,,C4225449,,616604,MONDO:0014707,14q32 duplication syndrome,14q32 duplication syndrome | 14q32 duplication syndrome (disorder) | Trisomy 14q32 | Predisposition to adult-onset myeloproliferative neoplasm due to 14q32 duplication
+BMGC_DS15988,BMG_DS060313,,CHROMOSOME 13q32 DELETION SYNDROME,,,,,,,C4225452,,156600,,,
+BMGC_DS15989,BMG_DS060314,,,,,,,,,C4225479,,613656,MONDO:0013344,"migraine, with or without aura, susceptibility to, 13",
+BMGC_DS15990,BMG_DS060315,,RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CATARACT,,,,,,,C4225493,,616722;610942,MONDO:0014747,familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome,
+BMGC_DS15991,BMG_DS060317,,"MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES",,,,,,,C4225499,,610436,,,
+BMGC_DS15992,BMG_DS060318,,SPERMATOGENIC FAILURE 6,,,,,,,C4225503,,102530;609856,,,
+BMGC_DS15993,BMG_DS060320,,IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH CARDIAC DEFECTS,,,,,,,C4225516,,608771,,,
+BMGC_DS15994,BMG_DS060331,,"ANEMIA, SIDEROBLASTIC, 1, LATE-ONSET",,,,,,,C4225593,,301300,,,
+BMGC_DS15995,BMG_DS060339,,CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME,,,,,,,C4225669,,612242,MONDO:0012830,chromosome 10q23 deletion syndrome,
+BMGC_DS15996,BMG_DS060341,,,,,,,,,C4225671,,192350,MONDO:0008642,VACTERL/vater association,
+BMGC_DS15997,BMG_DS060394,716196007,Isolated polycystic liver disease,,,,,,,C4255088,,,,,Isolated polycystic liver disease (disorder) | Isolated polycystic liver disease
+BMGC_DS15998,BMG_DS060396,,Bilateral Vestibulopathy,Bilateral Vestibulopathy,,,,,,C4255193,D000071699,,,,
+BMGC_DS15999,BMG_DS060614,,Colonic inflammatory bowel disease unclassified (IBDU),,DD72,Indeterminate colitis,K52.3,,,C4268603,,,,,
+BMGC_DS16000,BMG_DS060659,,Celiac disease with steatorrhea,,DA95,Coeliac disease,K90.0,,,C4268664,,,,,
+BMGC_DS16001,BMG_DS060756,,,,,,,,,C4272578,,,MONDO:0019026,autosomal recessive osteopetrosis,
+BMGC_DS16002,BMG_DS060760,764810000,Branchiootic syndrome,,,,,DOID:0060232,branchiootic syndrome,C4273131,C537104,,MONDO:0018878,branchiootic syndrome,Branchio-otic syndrome | Branchiootic syndrome (disorder) | Branchiootic syndrome
+BMGC_DS16003,BMG_DS060773,718227006,Proximal 16p11.2 microdeletion syndrome,,,,,DOID:0070515,"chromosome 16p11.2 deletion syndrome, 593-kb",C4273657,,,,,Proximal 16p11.2 microdeletion syndrome (disorder) | Proximal 16p11.2 microdeletion syndrome
+BMGC_DS16004,BMG_DS060776,718212006,TMEM70 related mitochondrial encephalo-cardio-myopathy,,,,,DOID:0060331,mitochondrial complex V (ATP synthase) deficiency nuclear type 2,C4273660,,,,,Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation (disorder) | Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation | TMEM70 related mitochondrial encephalo-cardio-myopathy
+BMGC_DS16005,BMG_DS060779,718194004,Hypothyroidism due to mutation in transcription factor of pituitary development,,,,,,,C4273672,,,MONDO:0016411,hypothyroidism due to deficient transcription factors involved in pituitary development or function,Hypothyroidism due to mutation in transcription factor of pituitary development (disorder) | Hypothyroidism due to mutation in transcription factor of pituitary development
+BMGC_DS16006,BMG_DS060785,718141008,Genetic steroid-resistant nephrotic syndrome,,,,,,,C4273714,,,MONDO:0019006,familial idiopathic steroid-resistant nephrotic syndrome,Familial idiopathic steroid-resistant nephrotic syndrome | Genetic steroid-resistant nephrotic syndrome (disorder) | Genetic steroid-resistant nephrotic syndrome | Hereditary steroid-resistant nephrotic syndrome
+BMGC_DS16007,BMG_DS060786,718124006,Fatal infantile cytochrome C oxidase deficiency,,,,,DOID:0050713,"COX deficiency, infantile mitochondrial myopathy",C4273730,,,MONDO:0015487,fatal infantile encephalocardiomyopathy,Fatal infantile cytochrome C oxidase deficiency (disorder) | Fatal infantile cytochrome C oxidase deficiency
+BMGC_DS16008,BMG_DS060787,718182008,Combined pituitary hormone deficiency genetic form,,,,,,,C4273747,,,MONDO:0013099,"combined pituitary hormone deficiencies, genetic form",Familial congenital hypopituitarism | Combined pituitary hormone deficiency genetic form (disorder) | Combined pituitary hormone deficiency genetic form | Multiple pituitary hormone deficiency genetic form
+BMGC_DS16009,BMG_DS060788,718183003,Familial thyroid dyshormonogenesis,,,,,,,C4273748,,,MONDO:0010132,familial thyroid dyshormonogenesis,Familial thyroid dyshormonogenesis (disorder) | Familial thyroid dyshormonogenesis
+BMGC_DS16010,BMG_DS060794,718228001,Fetal iodine syndrome,,,,,,,C4273860,,228355,MONDO:0009224,fetal iodine syndrome,Fetal iodine syndrome (disorder) | Fetal iodine syndrome | Foetal iodine syndrome
+BMGC_DS16011,BMG_DS060796,717633007,Distal monosomy 1q syndrome,,,,,,,C4273897,,,MONDO:0018205,distal monosomy 1q,Distal monosomy 1q | Distal deletion 1q | Monosomy 1qter | Telomeric deletion 1q | Distal monosomy 1q syndrome | Distal monosomy 1q syndrome (disorder)
+BMGC_DS16012,BMG_DS060798,717407006,Congenital plasminogen activator inhibitor deficiency type 1,,,,,,,C4273899,,,,,Congenital plasminogen activator inhibitor deficiency type 1 (disorder) | Congenital plasminogen activator inhibitor deficiency type 1
+BMGC_DS16013,BMG_DS060803,717269008,Obesity due to melanocortin 4 receptor deficiency,,,,,,,C4273958,,,MONDO:0019115,obesity due to melanocortin 4 receptor deficiency,Obesity due to melanocortin 4 receptor deficiency (disorder) | Obesity due to melanocortin 4 receptor deficiency
+BMGC_DS16014,BMG_DS060812,717254007,Familial pseudohyperkalemia,,,,,,,C4273970,,,,,Familial pseudohyperkalemia (disorder) | Familial pseudohyperkalemia | Familial pseudohyperkalaemia
+BMGC_DS16015,BMG_DS060816,717228004,Hereditary palmoplantar keratoderma Gamborg Nielsen type,,,,,DOID:0060862,mal de Meleda,C4273986,,244850,MONDO:0009489,"hereditary palmoplantar keratoderma, Gamborg-Nielsen type",Hereditary palmoplantar keratoderma Gamborg Nielsen type (disorder) | Hereditary palmoplantar keratoderma Gamborg Nielsen type
+BMGC_DS16016,BMG_DS060817,717225001,Benign adult familial myoclonic epilepsy,,,,,DOID:0111689,familial adult myoclonic epilepsy,C4273988,,,MONDO:0019448,benign adult familial myoclonic epilepsy,Benign adult familial myoclonic epilepsy (disorder) | Benign adult familial myoclonic epilepsy | BAFME - Benign adult familial myoclonic epilepsy | Autosomal dominant cortical myoclonus and epilepsy | Benign adult familial myoclonus epilepsy
+BMGC_DS16017,BMG_DS060820,717187000,Boichis syndrome,,,,,,,C4274018,,,MONDO:0019394,Senior-Boichis syndrome,Boichis disease | Nephronophthisis hepatic fibrosis syndrome (disorder) | Nephronophthisis hepatic fibrosis syndrome | Boichis syndrome
+BMGC_DS16018,BMG_DS060821,717182006,Hyperinsulinism due to deficiency of glucokinase,,,,,,,C4274019,,,,,Hyperinsulinism due to deficiency of glucokinase (disorder) | Hyperinsulinism due to deficiency of glucokinase | Hyperinsulinism due to glucokinase deficiency
+BMGC_DS16019,BMG_DS060824,717053007,Renal tubulopathy with encephalopathy and liver failure syndrome,,,,,,,C4274075,,,MONDO:0016811,renal tubulopathy-encephalopathy-liver failure syndrome,Renal tubulopathy with encephalopathy and liver failure syndrome (disorder) | Renal tubulopathy with encephalopathy and liver failure syndrome
+BMGC_DS16020,BMG_DS060825,717050005,Autosomal recessive sideroblastic anemia,,,,,,,C4274077,,,MONDO:0016828,autosomal recessive sideroblastic anemia,Autosomal recessive sideroblastic anemia (disorder) | Autosomal recessive sideroblastic anemia | Autosomal recessive sideroblastic anaemia
+BMGC_DS16021,BMG_DS060826,717048002,Hyperinsulinism due to HNF4A deficiency,,,,,,,C4274078,,,MONDO:0016988,hyperinsulinism due to HNF4A deficiency,Hyperinsulinism due to hepatocyte nuclear factor 4-alpha deficiency (disorder) | Hyperinsulinism due to hepatocyte nuclear factor 4-alpha deficiency | Hyperinsulinism due to HNF4A deficiency
+BMGC_DS16022,BMG_DS060828,717046003,Autosomal dominant hyperinsulinism due to SUR1 deficiency,,,,,,,C4274080,,,MONDO:0017184,autosomal dominant hyperinsulinism due to SUR1 deficiency,Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency (disorder) | Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency | Autosomal dominant hyperinsulinism due to SUR1 deficiency
+BMGC_DS16023,BMG_DS060829,717045004,Autosomal dominant hyperinsulinism due to Kir6.2 deficiency,,,,,,,C4274081,,,MONDO:0017185,autosomal dominant hyperinsulinism due to Kir6.2 deficiency,Autosomal dominant hyperinsulinism due to Kir6.2 deficiency (disorder) | Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
+BMGC_DS16024,BMG_DS060832,717042001,Pelizaeus Merzbacher like disease,,,,,,,C4274084,,,MONDO:0017226,Pelizaeus-Merzbacher-like disease,Pelizaeus Merzbacher like disease (disorder) | Pelizaeus Merzbacher like disease | PMLD - Pelizaeus Merzbacher like disease
+BMGC_DS16025,BMG_DS060833,717041008,Syndromic recessive X-linked ichthyosis,,,,,,,C4274085,,,MONDO:0017264,syndromic recessive X-linked ichthyosis,Syndromic recessive X-linked ichthyosis (disorder) | Syndromic recessive X-linked ichthyosis | Syndromic X-linked ichthyosis
+BMGC_DS16026,BMG_DS060834,716999001,Joubert syndrome with renal defect,,,,,,,C4274117,,,,,Joubert syndrome with renal defect (disorder) | Joubert syndrome with renal defect
+BMGC_DS16027,BMG_DS060835,716998009,Joubert syndrome with ocular defect,,,,,,,C4274118,,,MONDO:0016364,Joubert syndrome with ocular defect,Joubert syndrome with ocular defect (disorder) | Joubert syndrome with ocular defect | Joubert syndrome with retinopathy
+BMGC_DS16028,BMG_DS060843,716871006,Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency,,,,,,,C4274221,,,,,Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency (disorder) | Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency | Severe combined immunodeficiency due to DNA-PKcs deficiency
+BMGC_DS16029,BMG_DS060847,,,,,,,,,C4274282,,,MONDO:0005514,nanophthalmia,
+BMGC_DS16030,BMG_DS060853,716746003,Congenital alpha-2-antiplasmin deficiency,,,,,,,C4274304,,,,,Congenital alpha-2-antiplasmin deficiency (disorder) | Congenital alpha-2-antiplasmin deficiency | Congenital alpha2-antiplasmin deficiency
+BMGC_DS16031,BMG_DS060855,716743006,Familial non-autoimmune autosomal dominant hyperthyroidism,,,,,,,C4274306,,,,,Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder) | Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor | Familial non-immune hyperthyroidism | Familial non-autoimmune autosomal dominant hyperthyroidism
+BMGC_DS16032,BMG_DS060858,,,,,,,,,C4274324,,,MONDO:0020504,hereditary recurrent myoglobinuria,
+BMGC_DS16033,BMG_DS060861,716708005,FRAXF syndrome,,,,,,,C4274329,,,MONDO:0015084,FRAXF syndrome,FRAXF syndrome (disorder) | FRAXF syndrome
+BMGC_DS16034,BMG_DS060863,716857003,Hereditary pheochromocytoma and paraganglioma,,,,,,,C4274332,,,,,Hereditary pheochromocytoma and paraganglioma (disorder) | Hereditary pheochromocytoma and paraganglioma | Hereditary phaeochromocytoma and paraganglioma
+BMGC_DS16035,BMG_DS060865,716698007,Congenital deficiency of alpha-fetoprotein,,,,,,,C4274336,,,,,Congenital deficiency of alpha-fetoprotein (disorder) | Congenital deficiency of alpha-fetoprotein
+BMGC_DS16036,BMG_DS060872,716662004,Autosomal dominant late onset Parkinson disease,,,,,,,C4274355,,,,,Autosomal dominant late onset Parkinson disease (disorder) | Autosomal dominant late onset Parkinson disease | Hereditary late onset Parkinson disease
+BMGC_DS16037,BMG_DS060910,716232002,Autosomal dominant spondylocostal dysostosis,,,,,,,C4274761,,,MONDO:0015826,autosomal dominant spondylocostal dysostosis,Autosomal dominant spondylocostal dysostosis (disorder) | Autosomal dominant spondylocostal dysostosis | Autosomal dominant spondylocostal dysplasia
+BMGC_DS16038,BMG_DS060918,716869006,Mendelian susceptibility to mycobacterial disease due to complete IL12RB1 deficiency,,,,,,,C4274793,,,,,Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency (disorder) | Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | Mendelian susceptibility to mycobacterial disease due to complete IL12RB1 deficiency
+BMGC_DS16039,BMG_DS060920,716169009,Morse Rawnsley Sargent syndrome,,,,,,,C4274798,,,,,Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome (disorder) | Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome | Morse Rawnsley Sargent syndrome
+BMGC_DS16040,BMG_DS060928,716105001,Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type,,,,,,,C4274840,,,,,Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type | Non-epidermolytic palmoplantar keratoderma
+BMGC_DS16041,BMG_DS060935,716008002,Gingival fibromatosis and hypertrichosis syndrome,,,,,,,C4274889,,,,,Gingival fibromatosis and hypertrichosis syndrome (disorder) | Gingival fibromatosis and hypertrichosis syndrome | Hirsutism congenital gingival hyperplasia syndrome
+BMGC_DS16042,BMG_DS060943,715865008,Familial isolated arrhythmogenic right ventricular dysplasia,,,,,,,C4274968,,,MONDO:0016342,familial isolated arrhythmogenic right ventricular dysplasia,Familial isolated arrhythmogenic right ventricular dysplasia (disorder) | Familial isolated arrhythmogenic right ventricular dysplasia | Familial isolated ARVD (arrhythmogenic right ventricular dysplasia) | Familial isolated arrhythmogenic right ventricular cardiomyopathy
+BMGC_DS16043,BMG_DS060955,715817007,Lissencephaly with cerebellar hypoplasia,,,,,,,C4274995,,,MONDO:0019450,lissencephaly with cerebellar hypoplasia,Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder) | Lissencephaly co-occurrent with congenital cerebellar hypoplasia | Lissencephaly with cerebellar hypoplasia
+BMGC_DS16044,BMG_DS060957,715793003,Acetazolamide responsive myotonia,,,,,,,C4275008,,,MONDO:0020483,acetazolamide-responsive myotonia,Acetazolamide responsive myotonia (disorder) | Acetazolamide responsive myotonia
+BMGC_DS16045,BMG_DS060958,715780008,Lissencephaly type 1 due to doublecortin gene mutation,,,,,,,C4275012,,,,,Lissencephaly type 1 due to doublecortin gene mutation (disorder) | Lissencephaly type 1 due to doublecortin gene mutation | X-linked lissencephaly type 1
+BMGC_DS16046,BMG_DS060962,,,,,,,DOID:0111714,Mulchandani-Bhoj-Conlin syndrome,C4275029,,617352,MONDO:0019917,maternal uniparental disomy of chromosome 20,
+BMGC_DS16047,BMG_DS060963,715669000,Intestinal epithelial dysplasia,,,,,,,C4275062,,,,,Congenital tufting enteropathy | Tufting enteropathy | Congenital epithelial dysplasia of intestine (disorder) | Congenital epithelial dysplasia of intestine | Intestinal epithelial dysplasia
+BMGC_DS16048,BMG_DS060964,715670004,Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early onset osteoarthritis,,,,,,,C4275063,,,,,Mild spondyloepiphyseal dysplasia with early onset osteoarthritis due to collagen type II alpha 1 mutation (disorder) | Mild spondyloepiphyseal dysplasia with early onset osteoarthritis due to collagen type II alpha 1 mutation | Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early onset osteoarthritis
+BMGC_DS16049,BMG_DS060967,715657008,Familial avascular necrosis of femoral head,,,,,,,C4275066,,,MONDO:0012126,familial avascular necrosis of femoral head,Familial avascular necrosis of head of femur (disorder) | Familial avascular necrosis of head of femur | Familial avascular necrosis of femoral head
+BMGC_DS16050,BMG_DS060968,715655000,Transthyretin related familial amyloid cardiomyopathy,,,,,,,C4275067,,,MONDO:0019441,ATTRV122I amyloidosis,Transthyretin related familial amyloid cardiomyopathy (disorder) | Transthyretin related familial amyloid cardiomyopathy | Transthyretin amyloid cardiopathy | ATTRV122I amyloidosis
+BMGC_DS16051,BMG_DS060970,715646003,Desmin related myopathy with Mallory body-like inclusions,,,,,,,C4275073,,,MONDO:0019398,desmin-related myopathy with Mallory body-like inclusions,Desmin related myopathy with Mallory body-like inclusions (disorder) | Desmin related myopathy with Mallory body-like inclusions | Early onset desmin related myopathy
+BMGC_DS16052,BMG_DS060971,715633008,Atypical Werner syndrome,,,,,,,C4275075,,,MONDO:0019321,atypical Werner syndrome,Atypical Werner syndrome (disorder) | Atypical Werner syndrome | Atypical progeroid syndrome
+BMGC_DS16053,BMG_DS060984,715266002,Infection of skin of eyelid and periocular region,,,,,,,C4275160,,,,,Infection of skin of eyelid and periocular region (disorder) | Infection of skin of eyelid and periocular region
+BMGC_DS16054,BMG_DS060986,715364001,Familial abdominal aortic aneurysm,,,,,,,C4275172,,,MONDO:0007031,familial abdominal aortic aneurysm,Familial abdominal aortic aneurysm (disorder) | Familial abdominal aortic aneurysm
+BMGC_DS16055,BMG_DS060987,715345007,Young onset Parkinson disease,,,,,,,C4275179,,,MONDO:0017279,young-onset Parkinson disease,Young onset Parkinson disease (disorder) | Young onset Parkinson disease | Young onset Parkinson's disease | Early onset Parkinson disease | Early onset Parkinson's disease
+BMGC_DS16056,BMG_DS060989,715338007,Fatal infantile lactic acidosis with methylmalonic aciduria,,,,,,,C4275183,,,,,Fatal infantile lactic acidosis co-occurrent with methylmalonic aciduria (disorder) | Fatal infantile lactic acidosis co-occurrent with methylmalonic aciduria | Fatal infantile lactic acidosis with methylmalonic aciduria
+BMGC_DS16057,BMG_DS060990,715240000,X-linked retinal dysplasia,,,,,,,C4275241,,312550,MONDO:0010722,X-linked retinal dysplasia,X-linked retinal dysplasia (disorder) | X-linked retinal dysplasia
+BMGC_DS16058,BMG_DS060994,715219001,Familial spontaneous pneumothorax,,,,,,,C4275252,,,,,Familial spontaneous pneumothorax (disorder) | Familial spontaneous pneumothorax
+BMGC_DS16059,BMG_DS061002,,Chemical and Drug Induced Liver Injury,Chemical and Drug Induced Liver Injury,,,,,,C4277682,D056486,,,,
+BMGC_DS16060,BMG_DS061003,,,,,,,,,C4277690,,,MONDO:0005308,ciliopathy,
+BMGC_DS16061,BMG_DS061005,,Chemically-Induced Liver Toxicity,Chemical and Drug Induced Liver Injury,,,,,,C4279912,D056486,,,,
+BMGC_DS16062,BMG_DS061162,,,,,,,,,C4281559,,305620,MONDO:0024550,frontometaphyseal dysplasia 1,
+BMGC_DS16063,BMG_DS061164,,Childhood Absence Epilepsy,"Epilepsy, Absence",,,,DOID:0070309,absence epilepsy,C4281785,D004832,,MONDO:0010826,childhood absence epilepsy,
+BMGC_DS16064,BMG_DS061167,,,,,,,,,C4282128,,607411,MONDO:0024560,PDA1,
+BMGC_DS16065,BMG_DS061168,,,,,,,,,C4282179,,608907,MONDO:0012153,Alzheimer disease 9,
+BMGC_DS16066,BMG_DS061169,38795005,Sialidase deficiency,,,,,,,C4282398,C537366,256150;256550,MONDO:0009738,sialidosis type 2,"Sialidosis | Neuroaminidase deficiency | Sialidase deficiency | Mucolipidosis I | Mucolipidosis, type I | Sialidosis (disorder) | Mucolipidosis type I | Neuraminidase deficiency"
+BMGC_DS16067,BMG_DS061170,,,,,,,,,C4282400,,174200,MONDO:0008266,"polydactyly, postaxial, type A1",
+BMGC_DS16068,BMG_DS061171,722488009,Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency,,,,,,,C4283745,,,,,Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency (disorder) | Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency | Methacrylic aciduria | Valine metabolic defect | HIBCH-gene related deficiency of 3-hydroxyisobutyryl coenzyme A hydrolase | Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency
+BMGC_DS16069,BMG_DS061174,,"DEAFNESS, AUTOSOMAL DOMINANT 66",,,,,,,C4283893,,603356;616969,MONDO:0014854,autosomal dominant nonsyndromic hearing loss 66,
+BMGC_DS16070,BMG_DS061175,,TONNE-KALSCHEUER SYNDROME,,,,,DOID:0112042,Tonne-Kalscheuer syndrome,C4283894,,300978;300379,MONDO:0010506,"intellectual disability, X-linked 61",
+BMGC_DS16071,BMG_DS061177,,MIRAGE SYNDROME,,,,,,,C4284088,,610456;617053,MONDO:0014888,MIRAGE syndrome,
+BMGC_DS16072,BMG_DS061178,,"FANCONI ANEMIA, COMPLEMENTATION GROUP R",,,,,DOID:0111090,Fanconi anemia complementation group R,C4284093,,179617;617244,MONDO:0014986,Fanconi anemia complementation group R,
+BMGC_DS16073,BMG_DS061180,,"AORTIC ANEURYSM, FAMILIAL THORACIC 10",,,,,,,C4284414,,153455;617168,MONDO:0014950,"aortic aneurysm, familial thoracic 10",
+BMGC_DS16074,BMG_DS061181,,"SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE",,,,,,,C4284588,,611604;615681,MONDO:0014302,hereditary spastic paraplegia 62,
+BMGC_DS16075,BMG_DS061182,,"SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY",,,,,,,C4284592,,615759;617296,MONDO:0015007,"spastic paraplegia, intellectual disability, nystagmus, and obesity",
+BMGC_DS16076,BMG_DS061183,,BAND HETEROTOPIA,,,,,,,C4284594,,602033;600348,MONDO:0010873,band heterotopia of brain,
+BMGC_DS16077,BMG_DS061184,,PATENT DUCTUS ARTERIOSUS 2,,,,,,,C4284595,,617035;601601,MONDO:0014878,patent ductus arteriosus 2,
+BMGC_DS16078,BMG_DS061185,,,,,,,,,C4284790,,236670,MONDO:0009364,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1",
+BMGC_DS16079,BMG_DS061186,,METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA,,,,,DOID:0112316,methemoglobinemia and ambiguous genitalia,C4285231,,250790;613218,MONDO:0009605,methemoglobinemia type 4,
+BMGC_DS16080,BMG_DS061188,,Post-Cardiac Arrest Syndrome,Post-Cardiac Arrest Syndrome,,,,DOID:0070306,post-cardiac arrest syndrome,C4285706,D000080942,,MONDO:0850092,post-cardiac arrest syndrome,
+BMGC_DS16081,BMG_DS061194,,,,,,,DOID:7408,vulvar keratoacanthoma,C4288007,,,,,
+BMGC_DS16082,BMG_DS061202,,,,,,,DOID:5169,ovarian endometrioid stromal sarcoma,C4288544,,,MONDO:0003312,ovarian endometrioid stromal and related neoplasms,
+BMGC_DS16083,BMG_DS061205,,,,,,,,,C4289581,,,MONDO:0033980,RELA fusion-positive ependymoma,
+BMGC_DS16084,BMG_DS061206,,,,,,,DOID:5171,vaginal endometrial stromal tumor,C4289585,,,MONDO:0003314,endometrioid stromal and related neoplasms of the vagina,
+BMGC_DS16085,BMG_DS061207,,,,,,,DOID:4521,cervix endometrial stromal tumor,C4289586,,,MONDO:0003031,endometrioid stromal and related neoplasms of the cervix,
+BMGC_DS16086,BMG_DS061211,,,,,,,DOID:8338,villoglandular variant cervical mucinous adenocarcinoma,C4289808,,,MONDO:0006141,cervical villoglandular adenocarcinoma,
+BMGC_DS16087,BMG_DS061216,,,,,,,,,C4289994,,,MONDO:0100317,deficiency of adenosine deaminase 2,
+BMGC_DS16088,BMG_DS061217,,acute flaccid myelitis,,,,,DOID:0080947,acute flaccid myelitis,C4290000,C000629404,,MONDO:0100115,acute flaccid myelitis,
+BMGC_DS16089,BMG_DS061223,,diseases of the central nervous system caused by prions,,,,A81,,,C4290047,,,,,
+BMGC_DS16090,BMG_DS061237,,megaloblastic anemia unresponsive to vitamin B12 or folate therapy,,,,D53,,,C4290087,,,,,
+BMGC_DS16091,BMG_DS061239,,diabetes (mellitus) due to autoimmune process,,,,E10,DOID:0110755;DOID:0110753;DOID:0110747;DOID:0110761;DOID:0110751;DOID:0110754;DOID:0110742;DOID:0110749;DOID:0110752;DOID:0110759;DOID:0110758;DOID:0110756;DOID:0110760;DOID:0110746;DOID:0110757;DOID:0110745;DOID:0110741;DOID:0110743;DOID:0110750;DOID:0110744,type 1 diabetes mellitus 12 | type 1 diabetes mellitus 19 | type 1 diabetes mellitus 22 | type 1 diabetes mellitus 2 | type 1 diabetes mellitus 5 | type 1 diabetes mellitus 10 | type 1 diabetes mellitus 13 | type 1 diabetes mellitus 6 | type 1 diabetes mellitus 17 | type 1 diabetes mellitus 24 | type 1 diabetes mellitus 23 | type 1 diabetes mellitus 8 | type 1 diabetes mellitus 20 | type 1 diabetes mellitus 11 | type 1 diabetes mellitus 4 | type 1 diabetes mellitus 3 | type 1 diabetes mellitus 21 | type 1 diabetes mellitus 15 | type 1 diabetes mellitus 18 | type 1 diabetes mellitus 7,C4290090,,,,,
+BMGC_DS16092,BMG_DS061240,,diabetes (mellitus) due to immune mediated pancreatic islet beta-cell destruction,,,,E10,DOID:0110755;DOID:0110753;DOID:0110747;DOID:0110761;DOID:0110751;DOID:0110754;DOID:0110742;DOID:0110749;DOID:0110752;DOID:0110759;DOID:0110758;DOID:0110756;DOID:0110760;DOID:0110746;DOID:0110757;DOID:0110745;DOID:0110741;DOID:0110743;DOID:0110750;DOID:0110744,type 1 diabetes mellitus 12 | type 1 diabetes mellitus 19 | type 1 diabetes mellitus 22 | type 1 diabetes mellitus 2 | type 1 diabetes mellitus 5 | type 1 diabetes mellitus 10 | type 1 diabetes mellitus 13 | type 1 diabetes mellitus 6 | type 1 diabetes mellitus 17 | type 1 diabetes mellitus 24 | type 1 diabetes mellitus 23 | type 1 diabetes mellitus 8 | type 1 diabetes mellitus 20 | type 1 diabetes mellitus 11 | type 1 diabetes mellitus 4 | type 1 diabetes mellitus 3 | type 1 diabetes mellitus 21 | type 1 diabetes mellitus 15 | type 1 diabetes mellitus 18 | type 1 diabetes mellitus 7,C4290091,,,,,
+BMGC_DS16093,BMG_DS061241,,idiopathic diabetes (mellitus),,,,E10,DOID:0110755;DOID:0110753;DOID:0110747;DOID:0110761;DOID:0110751;DOID:0110754;DOID:0110742;DOID:0110749;DOID:0110752;DOID:0110759;DOID:0110758;DOID:0110756;DOID:0110760;DOID:0110746;DOID:0110757;DOID:0110745;DOID:0110741;DOID:0110743;DOID:0110750;DOID:0110744,type 1 diabetes mellitus 12 | type 1 diabetes mellitus 19 | type 1 diabetes mellitus 22 | type 1 diabetes mellitus 2 | type 1 diabetes mellitus 5 | type 1 diabetes mellitus 10 | type 1 diabetes mellitus 13 | type 1 diabetes mellitus 6 | type 1 diabetes mellitus 17 | type 1 diabetes mellitus 24 | type 1 diabetes mellitus 23 | type 1 diabetes mellitus 8 | type 1 diabetes mellitus 20 | type 1 diabetes mellitus 11 | type 1 diabetes mellitus 4 | type 1 diabetes mellitus 3 | type 1 diabetes mellitus 21 | type 1 diabetes mellitus 15 | type 1 diabetes mellitus 18 | type 1 diabetes mellitus 7,C4290092,,,,,
+BMGC_DS16094,BMG_DS061242,,diabetes (mellitus) due to insulin secretory defect,,,,E11,,,C4290093,,,,,
+BMGC_DS16095,BMG_DS061246,,the listed conditions whether the disorder is in the pituitary or the hypothalamus,,,,E23,,,C4290097,,,,,
+BMGC_DS16096,BMG_DS061252,,Alzheimer's dementia senile and presenile forms,,,,G30,DOID:0110035;DOID:0110037;DOID:0110038;DOID:0110047;DOID:0110039;DOID:0110044;DOID:0110048;DOID:0110043;DOID:0110041;DOID:0110046;DOID:0110045,Alzheimer's disease 15 | Alzheimer's disease 12 | Alzheimer's disease 2 | Alzheimer's disease 13 | Alzheimer's disease 6 | Alzheimer's disease 14 | Alzheimer's disease 5 | Alzheimer's disease 7 | Alzheimer's disease 10 | Alzheimer's disease 8 | Alzheimer's disease 11,C4290121,,,,,
+BMGC_DS16097,BMG_DS061277,,endarteritis deformans or obliterans,,,,I70,,,C4290148,,,,,
+BMGC_DS16098,BMG_DS061339,,Leser-Trélat disease,,,,L82,,,C4290219,,,,,
+BMGC_DS16099,BMG_DS061349,,cervicothoracic disc disorders with cervicalgia,,,,M50,,,C4290229,,,,,
+BMGC_DS16100,BMG_DS061350,,cervicothoracic disc disorders,,,,M50,,,C4290230,,,,,
+BMGC_DS16101,BMG_DS061370,,,,,,,,,C4296896,,,MONDO:0015524,hyperplastic polyposis syndrome,
+BMGC_DS16102,BMG_DS061500,722849002,Cryptogenic multifocal ulcerous stenosing enteritis,,,,,,,C4302263,,,MONDO:0018765,cryptogenic multifocal ulcerous stenosing enteritis,Cryptogenic multifocal ulcerous stenosing enteritis (disorder) | Cryptogenic multifocal ulcerous stenosing enteritis
+BMGC_DS16103,BMG_DS061566,722475006,X-linked congenital dyserythropoietic anemia with thrombocytopenia,,,,,,,C4302508,,,MONDO:0019031,thrombocytopenia with congenital dyserythropoietic anemia,X-linked congenital dyserythropoietic anemia with thrombocytopenia (disorder) | X-linked congenital dyserythropoietic anemia with thrombocytopenia | X-linked congenital dyserythropoietic anaemia with thrombocytopenia
+BMGC_DS16104,BMG_DS061576,722457005,"Juvenile cataract, microcornea, renal glucosuria syndrome",,,,,,,C4302529,,,,,"Juvenile cataract, microcornea, renal glucosuria syndrome (disorder) | Juvenile cataract, microcornea, renal glucosuria syndrome"
+BMGC_DS16105,BMG_DS061579,722436002,Dystrophic epidermolysis bullosa nails only,,,,,,,C4302547,,,MONDO:0015553,"dystrophic epidermolysis bullosa, nails only",Dystrophic epidermolysis bullosa nails only (disorder) | Dystrophic epidermolysis bullosa nails only | Nails only DEB (dystrophic epidermolysis bullosa)
+BMGC_DS16106,BMG_DS061580,722434004,Dysspondyloenchondromatosis,,,,,,,C4302548,,,MONDO:0019412,dysspondyloenchondromatosis,Dysspondyloenchondromatosis (disorder) | Dysspondyloenchondromatosis
+BMGC_DS16107,BMG_DS061589,722389002,Congenital hereditary facial paralysis with variable hearing loss syndrome,,,,,,,C4302592,,,MONDO:0017627,congenital hereditary facial paralysis-variable hearing loss syndrome,Congenital hereditary facial paralysis with variable hearing loss syndrome (disorder) | Congenital hereditary facial paralysis with variable hearing loss syndrome | Congenital hereditary facial palsy with variable deafness
+BMGC_DS16108,BMG_DS061599,722294004,Autosomal dominant intermediate Charcot-Marie-Tooth disease type E,,,,,,,C4302667,,614455,MONDO:0013758,Charcot-Marie-Tooth disease dominant intermediate E,Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (disorder) | Autosomal dominant intermediate Charcot-Marie-Tooth disease type E | Charcot-Marie-Tooth disease with nephropathy syndrome
+BMGC_DS16109,BMG_DS061600,722293005,"Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome",,,,,,,C4302668,,,,,"Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (disorder) | Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome"
+BMGC_DS16110,BMG_DS061601,722292000,Autosomal dominant beta2-microglobulinic amyloidosis,,,,,,,C4302669,,,MONDO:0017810,variant ABeta2M amyloidosis,Autosomal dominant beta2-microglobulinic amyloidosis (disorder) | Autosomal dominant beta2-microglobulinic amyloidosis | Variant ABeta2M amyloidosis
+BMGC_DS16111,BMG_DS061602,722288007,Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome,,,,,,,C4302671,,,,,Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome (disorder) | Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome
+BMGC_DS16112,BMG_DS061607,722283003,"Agnathia, holoprosencephaly, situs inversus syndrome",,,,,,,C4302678,,,,,"Agnathia, holoprosencephaly, situs inversus syndrome (disorder) | Agnathia, holoprosencephaly, situs inversus syndrome"
+BMGC_DS16113,BMG_DS061608,722282008,"Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome",,,,,,,C4302679,,,,,"Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (disorder) | Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome | Graham Cox syndrome"
+BMGC_DS16114,BMG_DS061620,722212004,Severe X-linked mitochondrial encephalomyopathy,,,,,,,C4302745,,,,,Severe X-linked mitochondrial encephalomyopathy (disorder) | Severe X-linked mitochondrial encephalomyopathy | Mitochondrial encephalomyopathy due to combined oxidative phosphorylation deficiency 6 | Mitochondrial encephalomyopathy due to COXPD6 deficiency
+BMGC_DS16115,BMG_DS061622,722202006,"Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome",,,,,,,C4302748,,,,,"Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) | Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome"
+BMGC_DS16116,BMG_DS061632,722122000,"Overgrowth, macrocephaly, facial dysmorphism syndrome",,,,,,,C4302813,,,,,"Overgrowth, macrocephaly, facial dysmorphism syndrome (disorder) | Overgrowth, macrocephaly, facial dysmorphism syndrome | Ring finger protein 135 related overgrowth syndrome | RNF135 (ring finger protein 135) related overgrowth syndrome"
+BMGC_DS16117,BMG_DS061635,722117000,"Osteosclerosis, developmental delay, craniosynostosis syndrome",,,,,,,C4302818,,,MONDO:0015800,osteosclerosis-developmental delay-craniosynostosis syndrome,"Osteosclerosis, developmental delay, craniosynostosis syndrome (disorder) | Osteosclerosis, developmental delay, craniosynostosis syndrome"
+BMGC_DS16118,BMG_DS061657,722053001,Obesity due to prohormone convertase I deficiency,,,,,,,C4302878,,,,,Obesity due to prohormone convertase I deficiency (disorder) | Obesity due to prohormone convertase I deficiency
+BMGC_DS16119,BMG_DS061667,722036008,"Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome",,,,,,,C4302893,,,MONDO:0019375,megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome,"Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome (disorder) | Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome | MPPH syndrome | MPPH (megalencephaly, polymicrogyria, polydactyly, hydrocephalus) syndrome"
+BMGC_DS16120,BMG_DS061746,721881008,Microduplication Xp11.22p11.23 syndrome,,,,,,,C4303068,,,,,Microduplication Xp11.22p11.23 syndrome (disorder) | Microduplication Xp11.22p11.23 syndrome | Trisomy Xp11.22-p11.23
+BMGC_DS16121,BMG_DS061747,721876004,Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency,,,,,,,C4303071,,,MONDO:0017900,autosomal recessive Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency,Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency (disorder) | Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency | Mendelian susceptibility to mycobacterial disease due to complete IFNgammaR2 deficiency
+BMGC_DS16122,BMG_DS061751,721840000,"Hyperuricemia, anemia, renal failure syndrome",,,,,,,C4303080,,,,,"Hyperuricemia, anemia, renal failure syndrome (disorder) | Hyperuricemia, anemia, renal failure syndrome | Hyperuricaemia, anaemia, renal failure syndrome | Familial juvenile hyperuricemic nephropathy type 2 | Familial juvenile hyperuricaemic nephropathy type 2 | Renin associated familial juvenile hyperuricemic nephropathy | Renin associated familial juvenile hyperuricaemic nephropathy"
+BMGC_DS16123,BMG_DS061753,721834007,Hyperinsulinism due to uncoupling protein 2 deficiency,,,,,,,C4303082,,,MONDO:0017183,hyperinsulinism due to UCP2 deficiency,Hyperinsulinism due to uncoupling protein 2 deficiency (disorder) | Hyperinsulinism due to uncoupling protein 2 deficiency | Hyperinsulinism due to UCP2 deficiency | Hyperinsulinism due to UCP2 (uncoupling protein 2) deficiency
+BMGC_DS16124,BMG_DS061816,721742004,Otitis media caused by Streptococcus pneumoniae,,,,,,,C4303152,,,,,Otitis media caused by Streptococcus pneumoniae (disorder) | Otitis media caused by Streptococcus pneumoniae | Streptococcus pneumoniae otitis media
+BMGC_DS16125,BMG_DS061928,,,,,,,DOID:0070324,systemic Epstein-Barr virus positive T-cell lymphoma of childhood,C4303422,,,,,
+BMGC_DS16126,BMG_DS061970,721236002,Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency,,,,,,,C4303473,,,,,Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder) | Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency | Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
+BMGC_DS16127,BMG_DS061971,721235003,Hyperinsulinism due to insulin receptor deficiency,,,,,,,C4303474,,,,,Hyperinsulinism due to insulin receptor deficiency (disorder) | Hyperinsulinism due to insulin receptor deficiency | Hyperinsulinism due to INSR (insulin receptor) deficiency
+BMGC_DS16128,BMG_DS061972,721234004,Hyperinsulinism due to HNF1A deficiency,,,,,,,C4303475,,,MONDO:0017935,hyperinsulinism due to HNF1A deficiency,Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency (disorder) | Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency | Hyperinsulinism due to HNF1A deficiency
+BMGC_DS16129,BMG_DS061975,721225009,Homocystinuria without methylmalonic aciduria,,,,,,,C4303479,,,MONDO:0018964,homocystinuria without methylmalonic aciduria,Homocystinuria without methylmalonic aciduria (disorder) | Homocystinuria without methylmalonic aciduria | Functional methionine synthase deficiency
+BMGC_DS16130,BMG_DS061977,721219005,Familial Alzheimer-like prion disease,,,,,,,C4303482,,,MONDO:0017233,familial Alzheimer-like prion disease,Familial Alzheimer-like prion disease (disorder) | Familial Alzheimer-like prion disease
+BMGC_DS16131,BMG_DS062019,717942003,Brain dopamine-serotonin vesicular transport disease,,,,,DOID:0070490,infantile parkinsonism-dystonia 2,C4303546,,618049,MONDO:0018130,brain dopamine-serotonin vesicular transport disease,Brain dopamine-serotonin vesicular transport disease (disorder) | Brain dopamine-serotonin vesicular transport disease
+BMGC_DS16132,BMG_DS062023,717909004,Bilateral microtia with deafness and cleft palate syndrome,,,,,,,C4303551,,,,,Bilateral microtia with deafness and cleft palate syndrome (disorder) | Bilateral microtia with deafness and cleft palate syndrome
+BMGC_DS16133,BMG_DS062024,718751000,COG4 congenital disorder of glycosylation,,,,,,,C4303552,,613489,MONDO:0013281,COG4-congenital disorder of glycosylation,Carbohydrate deficient glycoprotein syndrome type 2j | Carbohydrate deficient glycoprotein syndrome type IIj | CDG2J - carbohydrate deficient glycoprotein syndrome type 2J | Component of oligomeric golgi complex 4 congenital disorder of glycosylation (disorder) | Component of oligomeric golgi complex 4 congenital disorder of glycosylation | COG4 (component of oligomeric golgi complex 4) congenital disorder of glycosylation | COG4 congenital disorder of glycosylation
+BMGC_DS16134,BMG_DS062029,717821004,Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency,,,,,,,C4303568,,,,,Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency (disorder) | Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | Glycogen storage disease type 15 | Glycogen storage disease type XV | Glycogenosis with severe cardiomyopathy due to glycogenin deficiency
+BMGC_DS16135,BMG_DS062037,721092005,"Developmental malformation, deafness, dystonia syndrome",,,,,,,C4303590,,,,,"Developmental malformation, deafness, dystonia syndrome (disorder) | Developmental malformation, deafness, dystonia syndrome"
+BMGC_DS16136,BMG_DS062039,721088003,DEND syndrome,,,,,,,C4303593,,,MONDO:0019207,DEND syndrome,"Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | Developmental delay, epilepsy, neonatal diabetes syndrome | DEND syndrome | DEND (developmental delay, epilepsy, neonatal diabetes) syndrome"
+BMGC_DS16137,BMG_DS062042,721074002,Short stature due to primary acid labile subunit deficiency,,,,,,,C4303612,,,,,Short stature due to primary acid labile subunit deficiency (disorder) | Short stature due to primary acid labile subunit deficiency
+BMGC_DS16138,BMG_DS062043,721072003,"Short stature, pituitary and cerebellar defect and small sella turcica syndrome",,,,,,,C4303613,,,,,"Short stature, pituitary and cerebellar defect and small sella turcica syndrome (disorder) | Short stature, pituitary and cerebellar defect and small sella turcica syndrome"
+BMGC_DS16139,BMG_DS062046,721877008,Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency,,,,,,,C4303665,,,,,Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency (disorder) | Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | Mendelian susceptibility to mycobacterial disease due to complete IL12B deficiency
+BMGC_DS16140,BMG_DS062051,721882001,Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome,,,,,,,C4303670,,,,,Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome (disorder) | Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome | ATRUS syndrome
+BMGC_DS16141,BMG_DS062083,720986005,"Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome",,,,,,,C4303737,,300301,MONDO:0010295,anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome,"Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome (disorder) | Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome | Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema syndrome | OL-EDA-ID (anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema) syndrome | OL-EDA-ID (anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema) syndrome"
+BMGC_DS16142,BMG_DS062092,720951008,Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3,,,,,,,C4303760,,,,,Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (disorder) | Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | Combined oxidative phosphorylation deficiency type 3
+BMGC_DS16143,BMG_DS062093,720950009,Familial thrombocytosis,,,,,,,C4303761,,,MONDO:0019111,familial thrombocytosis,Familial thrombocytosis (disorder) | Familial thrombocytosis | Familial thrombocythemia | Hereditary thrombocythaemia | Hereditary thrombocythemia | Familial thrombocythaemia
+BMGC_DS16144,BMG_DS062094,720864008,Encephalopathy due to prosaposin deficiency,,,,,,,C4303785,,,,,Encephalopathy due to prosaposin deficiency (disorder) | Encephalopathy due to prosaposin deficiency | Combined prosaposin deficiency | Combined saposin deficiency
+BMGC_DS16145,BMG_DS062096,720859009,Ehlers-Danlos syndrome kyphoscoliotic and deafness type,,,,,,,C4303788,,,,,"Ehlers-Danlos syndrome kyphoscoliotic and deafness type (disorder) | Ehlers-Danlos syndrome kyphoscoliotic and deafness type | Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and deafness | Ehlers-Danlos syndrome kyphoscoliotic and hearing loss type | Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency"
+BMGC_DS16146,BMG_DS062097,720858001,Ehlers-Danlos syndrome cardiac valvular type,,,,,,,C4303789,,225320,MONDO:0009159,"Ehlers-Danlos syndrome, cardiac valvular type",Ehlers-Danlos syndrome cardiac valvular type (disorder) | Ehlers-Danlos syndrome cardiac valvular type
+BMGC_DS16147,BMG_DS062099,720853005,"Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome",,,,,,,C4303792,,,,,"Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome (disorder) | Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionising radiation syndrome | Cernunnos-XLF deficiency | Severe combined immunodeficiency due to Cernunnos protein deficiency | NHEJ1 (non-homologous end joining factor) syndrome"
+BMGC_DS16148,BMG_DS062101,720831008,Deficiency of cathepsin D,,,,,,,C4303804,,,,,Deficiency of cathepsin D (disorder) | Deficiency of cathepsin D | Cathepsin D deficiency
+BMGC_DS16149,BMG_DS062105,720756005,Craniofacial ulnar renal syndrome,,,,,,,C4303860,,,MONDO:0017398,3MC syndrome,Craniofacial ulnar renal syndrome (disorder) | Craniofacial ulnar renal syndrome | 3MC syndrome
+BMGC_DS16150,BMG_DS062128,720521008,Autosomal dominant macrothrombocytopenia,,,,,,,C4304021,,,MONDO:0015372,autosomal dominant macrothrombocytopenia,Autosomal dominant macrothrombocytopenia (disorder) | Autosomal dominant macrothrombocytopenia
+BMGC_DS16151,BMG_DS062129,720520009,Attenuated Chédiak-Higashi syndrome,,,,,,,C4304022,,,MONDO:0018133,attenuated Chédiak-Higashi syndrome,Attenuated Chédiak-Higashi syndrome (disorder) | Attenuated Chédiak-Higashi syndrome | Atypical Chédiak-Higashi syndrome
+BMGC_DS16152,BMG_DS062132,720506002,Deafness and myopia syndrome,,,,,,,C4304026,,,,,Deafness and myopia syndrome (disorder) | Deafness and myopia syndrome | High myopia and sensorineural deafness
+BMGC_DS16153,BMG_DS062142,720465002,Adult-onset autosomal recessive sideroblastic anemia,,,,,,,C4304054,,,,,Adult-onset autosomal recessive sideroblastic anemia (disorder) | Adult-onset autosomal recessive sideroblastic anemia | GLRX5 (glutaredoxin 5) related sideroblastic anemia | GLRX5 (glutaredoxin 5) related sideroblastic anaemia | Adult-onset autosomal recessive sideroblastic anaemia
+BMGC_DS16154,BMG_DS062143,720463009,Adducted thumbs and arthrogryposis syndrome Christian type,,,,,,,C4304055,,201550,MONDO:0008724,"adducted thumbs-arthrogryposis syndrome, Christian type",Adducted thumbs and arthrogryposis syndrome Christian type (disorder) | Adducted thumbs and arthrogryposis syndrome Christian type
+BMGC_DS16155,BMG_DS062144,720461006,Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein,,,,,,,C4304057,,,,,Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein (disorder) | Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein
+BMGC_DS16156,BMG_DS062165,719985001,Autosomal dominant limb girdle muscular dystrophy type 1A,,,,,,,C4304304,,,,,Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) | Autosomal dominant limb girdle muscular dystrophy type 1A | Limb girdle muscular dystrophy due to myotilin deficiency | Limb-girdle muscular dystrophy 1A myotilin myopathy
+BMGC_DS16157,BMG_DS062170,719907006,Timothy syndrome type 2,,,,,,,C4304347,,,MONDO:0035679,Timothy syndrome type 2,Timothy syndrome type 2 (disorder) | Timothy syndrome type 2
+BMGC_DS16158,BMG_DS062172,719865001,Influenza caused by pandemic influenza virus,,,,,,,C4304383,,,,,Influenza caused by pandemic influenza virus (disorder) | Influenza caused by pandemic influenza virus
+BMGC_DS16159,BMG_DS062178,719838008,X-linked hereditary sensory and autonomic neuropathy with deafness,,,,,,,C4304400,,300614,MONDO:0010378,X-linked hereditary sensory and autonomic neuropathy with hearing loss,X-linked hereditary sensory and autonomic neuropathy with deafness (disorder) | X-linked hereditary sensory and autonomic neuropathy with deafness | X-linked auditory neuropathy with peripheral sensory neuropathy type 1 | X-linked HSAN (hereditary sensory and autonomic neuropathy) with deafness
+BMGC_DS16160,BMG_DS062183,719819004,Xeroderma pigmentosum and Cockayne syndrome complex,,,,,,,C4304411,,,MONDO:0016354,xeroderma pigmentosum-Cockayne syndrome complex,Xeroderma pigmentosum and Cockayne syndrome complex (disorder) | Xeroderma pigmentosum and Cockayne syndrome complex
+BMGC_DS16161,BMG_DS062191,719688002,Multiple epiphyseal dysplasia Al-Gazali type,,,,,,,C4304500,,,,,Multiple epiphyseal dysplasia Al-Gazali type (disorder) | Multiple epiphyseal dysplasia Al-Gazali type | Multiple epiphyseal dysplasia and macrocephaly with distinctive facies syndrome
+BMGC_DS16162,BMG_DS062195,719646006,8p11.2 deletion syndrome,,,,,,,C4304505,,,MONDO:0016657,8p11.2 deletion syndrome,8p11.2 deletion syndrome (disorder) | 8p11.2 deletion syndrome | Monosomy 8p11.2
+BMGC_DS16163,BMG_DS062197,719666002,6q terminal deletion syndrome,,,,,,,C4304514,,,MONDO:0019164,6q terminal deletion syndrome,6q terminal deletion syndrome (disorder) | 6q terminal deletion syndrome
+BMGC_DS16164,BMG_DS062198,719665003,5q35 microduplication syndrome,,,,,,,C4304526,,,MONDO:0016461,5q35 microduplication syndrome,5q35 microduplication syndrome (disorder) | 5q35 microduplication syndrome | Trisomy 5q35
+BMGC_DS16165,BMG_DS062201,719661007,5q14.3 microdeletion syndrome,,,,,,,C4304529,,,MONDO:0016456,5q14.3 microdeletion syndrome,5q14.3 microdeletion syndrome (disorder) | 5q14.3 microdeletion syndrome | Monosomy 5q14.3
+BMGC_DS16166,BMG_DS062203,719659003,2q32q33 microdeletion syndrome,,,,,,,C4304531,,,,,2q32q33 microdeletion syndrome (disorder) | 2q32q33 microdeletion syndrome | Monosomy 2q32q33
+BMGC_DS16167,BMG_DS062204,719657001,2q23.1 microdeletion syndrome,,,,,,,C4304532,,,MONDO:0016459,2q23.1 microdeletion syndrome,2q23.1 microdeletion syndrome (disorder) | 2q23.1 microdeletion syndrome | Monosomy 2q23.1 | Pseudo-Angelman syndrome
+BMGC_DS16168,BMG_DS062205,719652007,2p21 microdeletion syndrome,,,,,,,C4304537,,,MONDO:0015583,2p21 microdeletion syndrome,2p21 microdeletion syndrome (disorder) | 2p21 microdeletion syndrome | Monosomy 2p21
+BMGC_DS16169,BMG_DS062207,719650004,20p12.3 microdeletion syndrome,,,,,,,C4304539,,,MONDO:0016841,20p12.3 microdeletion syndrome,20p12.3 microdeletion syndrome (disorder) | 20p12.3 microdeletion syndrome | Monosomy 20p12.3
+BMGC_DS16170,BMG_DS062208,719649004,1q44 microdeletion syndrome,,,,,,,C4304540,,,MONDO:0016561,1q44 microdeletion syndrome,1q44 microdeletion syndrome (disorder) | 1q44 microdeletion syndrome | Monosomy 1q44
+BMGC_DS16171,BMG_DS062210,719600006,1p21.3 microdeletion syndrome,,,,,,,C4304578,,,MONDO:0017405,1p21.3 microdeletion syndrome,1p21.3 microdeletion syndrome (disorder) | 1p21.3 microdeletion syndrome | Monosomy 1p21.3
+BMGC_DS16172,BMG_DS062212,719595002,Absence of fingerprints with congenital milia syndrome,,,,,,,C4304581,,,,,Absence of fingerprints with congenital milia syndrome (disorder) | Absence of fingerprints with congenital milia syndrome | Absence of dermatoglyphics with congenital milia syndrome | Baird syndrome
+BMGC_DS16173,BMG_DS062215,719584008,17q23.1q23.2 microdeletion syndrome,,,,,,,C4304591,,,,,17q23.1q23.2 microdeletion syndrome (disorder) | 17q23.1q23.2 microdeletion syndrome
+BMGC_DS16174,BMG_DS062226,719582007,17p13.3 microduplication syndrome,,,,,,,C4304641,,,,,17p13.3 microduplication syndrome (disorder) | 17p13.3 microduplication syndrome | Trisomy 17p13.3
+BMGC_DS16175,BMG_DS062240,719520001,Benign concentric annular macular dystrophy,,,,,,,C4304667,,,,,Benign concentric annular macular dystrophy (disorder) | Benign concentric annular macular dystrophy
+BMGC_DS16176,BMG_DS062242,719518004,Autosomal dominant palmoplantar keratoderma and congenital alopecia,,,,,,,C4304669,,104100,MONDO:0007083,autosomal dominant palmoplantar keratoderma and congenital alopecia,Autosomal dominant palmoplantar keratoderma and congenital alopecia (disorder) | Autosomal dominant palmoplantar keratoderma and congenital alopecia | Palmoplantar keratoderma and congenital alopecia Stevanovic type
+BMGC_DS16177,BMG_DS062243,719516000,Autosomal dominant focal dystonia DYT25 type,,,,,,,C4304670,,615073,MONDO:0014033,dystonia 25,Autosomal dominant focal dystonia DYT25 type (disorder) | Autosomal dominant focal dystonia DYT25 type
+BMGC_DS16178,BMG_DS062244,719514002,Autosomal dominant Charcot-Marie-Tooth disease type 2M,,,,,,,C4304672,,,MONDO:0016431,autosomal dominant Charcot-Marie-Tooth disease type 2M,Autosomal dominant Charcot-Marie-Tooth disease type 2M (disorder) | Autosomal dominant Charcot-Marie-Tooth disease type 2M
+BMGC_DS16179,BMG_DS062245,719513008,Autosomal dominant Charcot-Marie-Tooth disease type 2L,,,,,,,C4304673,,,,,Autosomal dominant Charcot-Marie-Tooth disease type 2L (disorder) | Autosomal dominant Charcot-Marie-Tooth disease type 2L
+BMGC_DS16180,BMG_DS062247,719454003,Congenital bile acid synthesis defect type 3,,,,,,,C4304715,,,,,Congenital bile acid synthesis defect type 3 (disorder) | Congenital bile acid synthesis defect type 3 | Oxysterol 7-alpha hydroxylase deficiency
+BMGC_DS16181,BMG_DS062250,719432000,Late-onset junctional epidermolysis bullosa,,,,,,,C4304724,,,MONDO:0019309,late-onset junctional epidermolysis bullosa,Late-onset junctional epidermolysis bullosa (disorder) | Late-onset junctional epidermolysis bullosa
+BMGC_DS16182,BMG_DS062251,719430008,Leber plus disease,,,,,,,C4304725,,,MONDO:0020478,Leber plus disease,Leber plus disease (disorder) | Leber plus disease
+BMGC_DS16183,BMG_DS062255,719405005,Leukoencephalopathy with metaphyseal chondrodysplasia syndrome,,,,,,,C4304743,,,,,Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Leukoencephalopathy with metaphyseal chondrodysplasia syndrome | Leucoencephalopathy with metaphyseal chondrodysplasia syndrome
+BMGC_DS16184,BMG_DS062266,719282008,Primary ciliary dyskinesia and retinitis pigmentosa syndrome,,,,,,,C4304829,,,,,Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Primary ciliary dyskinesia and retinitis pigmentosa syndrome
+BMGC_DS16185,BMG_DS062267,719272007,Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome,,,,,,,C4304831,,,MONDO:0016424,progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome,Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome (disorder) | Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome | Progressive sensorineural deafness and hypertrophic cardiomyopathy syndrome
+BMGC_DS16186,BMG_DS062268,719274008,Primary pigmented nodular adrenocortical disease,,,,,DOID:0060280,primary pigmented nodular adrenocortical disease,C4304832,,,MONDO:0015999,primary pigmented nodular adrenocortical disease,Primary pigmented nodular adrenocortical disease (disorder) | Primary pigmented nodular adrenocortical disease
+BMGC_DS16187,BMG_DS062270,719267003,Progressive cavitating leukoencephalopathy,,,,,,,C4304840,,,MONDO:0015349,progressive cavitating leukoencephalopathy,Progressive cavitating leukoencephalopathy (disorder) | Progressive cavitating leukoencephalopathy | Progressive cavitating leucoencephalopathy
+BMGC_DS16188,BMG_DS062272,719205008,Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome,,,,,,,C4304887,,,,,Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome (disorder) | Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome
+BMGC_DS16189,BMG_DS062277,719157002,X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome,,,,,,,C4304918,,,,,X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome (disorder) | X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome | X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behaviour syndrome
+BMGC_DS16190,BMG_DS062282,719136005,X-linked intellectual disability with cerebellar hypoplasia syndrome,,,,,,,C4304937,,,,,X-linked intellectual disability with cerebellar hypoplasia syndrome (disorder) | X-linked intellectual disability with cerebellar hypoplasia syndrome | OPHN1 syndrome | Oligophrenin-1 syndrome
+BMGC_DS16191,BMG_DS062291,719043002,VACTERL syndrome with hydrocephalus,,,,,,,C4305002,,,,,"Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-esophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus (disorder) | Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-esophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus | Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-oesophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus | VACTERL syndrome with hydrocephalus"
+BMGC_DS16192,BMG_DS062292,719042007,Uveal coloboma with cleft lip and palate and intellectual disability syndrome,,,,,,,C4305003,,,,,Uveal coloboma with cleft lip and palate and intellectual disability syndrome (disorder) | Uveal coloboma with cleft lip and palate and intellectual disability syndrome
+BMGC_DS16193,BMG_DS062295,719016007,X-linked intellectual disability Cantagrel type,,,,,,,C4305023,,,,,X-linked intellectual disability Cantagrel type (disorder) | X-linked intellectual disability Cantagrel type
+BMGC_DS16194,BMG_DS062302,718914002,X-linked intellectual disability Van Esch type,,,,,,,C4305072,,301030,MONDO:0015601,"X-linked intellectual disability, van Esch type",X-linked intellectual disability Van Esch type (disorder) | X-linked intellectual disability Van Esch type
+BMGC_DS16195,BMG_DS062305,718910006,X-linked intellectual disability Stocco Dos Santos type,,,,,,,C4305076,,,,,X-linked intellectual disability Stocco Dos Santos type (disorder) | X-linked intellectual disability Stocco Dos Santos type
+BMGC_DS16196,BMG_DS062307,718908009,X-linked intellectual disability Siderius type,,,,,,,C4305078,,,,,X-linked intellectual disability Siderius type (disorder) | X-linked intellectual disability Siderius type
+BMGC_DS16197,BMG_DS062309,718900002,Syndromic X-linked intellectual disability type 11,,,,,,,C4305085,,,,,Syndromic X-linked intellectual disability type 11 (disorder) | Syndromic X-linked intellectual disability type 11 | X-linked intellectual disability Shashi type
+BMGC_DS16198,BMG_DS062312,718881004,Chromosome Xq27.3q28 duplication syndrome,,,,,,,C4305103,,,,,Chromosome Xq27.3q28 duplication syndrome (disorder) | Chromosome Xq27.3q28 duplication syndrome
+BMGC_DS16199,BMG_DS062314,718851007,Cataract glaucoma syndrome,,,,,,,C4305131,,,MONDO:0015567,cataract-glaucoma syndrome,Cataract glaucoma syndrome (disorder) | Cataract glaucoma syndrome
+BMGC_DS16200,BMG_DS062316,718848000,Fried syndrome,,,,,,,C4305134,,,MONDO:0019428,fried syndrome,Fried syndrome (disorder) | Fried syndrome
+BMGC_DS16201,BMG_DS062320,719046005,12q14 microdeletion syndrome,,,,,,,C4305140,,,MONDO:0019784,12q14 microdeletion syndrome,12q14 microdeletion syndrome (disorder) | 12q14 microdeletion syndrome | Osteopoikilosis with short stature and intellectual disability syndrome | Monosomy 12q14
+BMGC_DS16202,BMG_DS062323,718766002,"Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome",,,,,,,C4305147,,618618,MONDO:0032835,"spondyloepiphyseal dysplasia, nishimura type","Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome (disorder) | Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome | Spondyloepiphyseal dysplasia Nishimura type"
+BMGC_DS16203,BMG_DS062325,,,,,,,,,C4305153,,611603,MONDO:0012703,lissencephaly due to TUBA1A mutation,
+BMGC_DS16204,BMG_DS062326,722008003,Isolated autosomal dominant hypomagnesemia Glaudemans type,,,,,,,C4305155,,,MONDO:0016048,"isolated autosomal dominant hypomagnesemia, Glaudemans type",Isolated autosomal dominant hypomagnesemia Glaudemans type (disorder) | Isolated autosomal dominant hypomagnesemia Glaudemans type | Isolated autosomal dominant hypomagnesaemia Glaudemans type
+BMGC_DS16205,BMG_DS062330,719575008,15q14 microdeletion syndrome,,,,,,,C4305230,,616898,MONDO:0014822,15q14 microdeletion syndrome,15q14 microdeletion syndrome (disorder) | 15q14 microdeletion syndrome | Monosomy 15q14
+BMGC_DS16206,BMG_DS062331,719574007,14q12 microdeletion syndrome,,,,,,,C4305240,,,MONDO:0016833,14q12 microdeletion syndrome,14q12 microdeletion syndrome (disorder) | 14q12 microdeletion syndrome | Monosomy 14q12
+BMGC_DS16207,BMG_DS062332,718721006,Congenital analbuminemia,,,,,,,C4305253,,616000,MONDO:0014449,congenital analbuminemia,Congenital analbuminemia (disorder) | Congenital analbuminemia | Congenital analbuminaemia
+BMGC_DS16208,BMG_DS062335,718717004,Primary immunodeficiency syndrome due to p14 deficiency,,,,,,,C4305256,,,,,Primary immunodeficiency syndrome due to p14 deficiency (disorder) | Primary immunodeficiency syndrome due to p14 deficiency | Primary immunodeficiency syndrome with short stature
+BMGC_DS16209,BMG_DS062338,718713000,Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome,,,,,,,C4305259,,,,,Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome
+BMGC_DS16210,BMG_DS062340,718690009,Congenital hypothyroidism due to absence of thyroid gland,,,,,,,C4305275,,,,,Congenital hypothyroidism due to absence of thyroid gland (disorder) | Congenital hypothyroidism due to absence of thyroid gland
+BMGC_DS16211,BMG_DS062342,718687003,Distal monosomy 10q syndrome,,,,,,,C4305277,,,,,Distal monosomy 10q | Distal deletion 10q | Distal monosomy 10q syndrome (disorder) | Distal monosomy 10q syndrome
+BMGC_DS16212,BMG_DS062345,,,,,,,,,C4305324,,,MONDO:0017268,acral self-healing collodion baby,
+BMGC_DS16213,BMG_DS062348,718551002,Moyamoya disease with early onset achalasia,,,,,,,C4305378,,,,,Moyamoya disease with early onset achalasia (disorder) | Moyamoya disease with early onset achalasia
+BMGC_DS16214,BMG_DS062352,,Wartenberg Syndrome,Radial Neuropathy,,,,,,C4305399,D020425,,,,
+BMGC_DS16215,BMG_DS062410,,Multi-Drug Resistant Nephrotic Syndrome,Nephrotic Syndrome,,,,,,C4305538,D009404,,,,
+BMGC_DS16216,BMG_DS062420,717705004,Mayer-Rokitansky-Küster-Hauser syndrome type 2,,,,,,,C4305568,,601076,MONDO:0010989,Mayer-Rokitansky-Küster-Hauser syndrome type 2,"Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) | Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Atypical MRKH (Mayer Rokitansky Kuster Hauser) syndrome | Mullerian duct aplasia, renal dysplasia, cervical somite anomalies syndrome"
+BMGC_DS16217,BMG_DS062428,,"Hypercalcemia, Infantile, 1",,,,,,,C4310232,C562999,143880,MONDO:0020739,"hypercalcemia, infantile, 1",
+BMGC_DS16218,BMG_DS062429,,"Hypercalcemia, infantile, 2",,,,,,,C4310473,C562999,616963,MONDO:0014851,"hypercalcemia, infantile, 2",
+BMGC_DS16219,BMG_DS062431,765435009,OTU deubiquitinase with linear linkage specificity related autoinflammatory syndrome (disorder),,,,,,,C4310614,,617099,MONDO:0014912,infantile-onset periodic fever-panniculitis-dermatosis syndrome,"Otulipenia | OTU deubiquitinase with linear linkage specificity related autoinflammatory syndrome (disorder) | OTULIN (OTU deubiquitinase with linear linkage specificity) related autoinflammatory syndrome | OTU deubiquitinase with linear linkage specificity related autoinflammatory syndrome | OTULIN-related autoinflammatory syndrome | Infantile-onset periodic fever, panniculitis, dermatosis syndrome"
+BMGC_DS16220,BMG_DS062432,,"ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE",,,,,DOID:0111652,ectodermal dysplasia 12,C4310616,,617337;616758,MONDO:0015024,"ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type",
+BMGC_DS16221,BMG_DS062433,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS,,,,,,,C4310617,,617333;602410,MONDO:0015022,intellectual developmental disorder with dysmorphic facies and ptosis,
+BMGC_DS16222,BMG_DS062434,,"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME",,,,,DOID:0081176,"hypotonia, ataxia, and delayed development syndrome",C4310618,,617330;607407,MONDO:0015021,"hypotonia, ataxia, and delayed development syndrome",
+BMGC_DS16223,BMG_DS062435,,,,,,,,,C4310619,,617323,MONDO:0015020,"intellectual disability, autosomal recessive 59",
+BMGC_DS16224,BMG_DS062436,768667002,Yao syndrome,,,,,,,C4310620,C000730393,617321,MONDO:0015019,Yao syndrome,Yao syndrome | Nucleotide binding oligomerization domain containing 2-associated autoinflammatory disease (disorder) | NOD2-associated autoinflammatory disease | Nucleotide binding oligomerization domain containing 2-associated autoinflammatory disease | NOD2 (nucleotide binding oligomerization domain containing 2) associated autoinflammatory disease
+BMGC_DS16225,BMG_DS062437,,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 12",,,,,,,C4310621,,605848;617320,MONDO:0015018,"ichthyosis, congenital, autosomal recessive 12",
+BMGC_DS16226,BMG_DS062438,,,,,,,,,C4310622,,617319,MONDO:0015017,anterior segment dysgenesis 8,
+BMGC_DS16227,BMG_DS062439,,ANTERIOR SEGMENT DYSGENESIS 6,,,,,DOID:0080611,anterior segment dysgenesis 6,C4310623,,617315;601771,MONDO:0015016,anterior segment dysgenesis 6,
+BMGC_DS16228,BMG_DS062440,,"BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6",,,,,DOID:0111067,congenital bile acid synthesis defect 6,C4310624,,617308;601641,MONDO:0015015,congenital bile acid synthesis defect 6,
+BMGC_DS16229,BMG_DS062441,,"COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS",,,,,,,C4310625,,617306;156845,MONDO:0015014,"coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness",
+BMGC_DS16230,BMG_DS062442,,RETINITIS PIGMENTOSA 77,,,,,,,C4310626,,617304;609346,MONDO:0015013,retinitis pigmentosa 77,
+BMGC_DS16231,BMG_DS062443,,MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME,,,,,,,C4310627,,617303;610034,MONDO:0015012,mucopolysaccharidosis-plus syndrome,
+BMGC_DS16232,BMG_DS062444,,OPTIC ATROPHY 11,,,,,DOID:0111436,optic atrophy 11,C4310628,,607472;617302,MONDO:0015011,optic atrophy 11,
+BMGC_DS16233,BMG_DS062445,,LYMPHATIC MALFORMATION 7,,,,,DOID:0081030,central conducting lymphatic anomaly,C4310629,,617300;600011,MONDO:0015009,lymphatic malformation 7,
+BMGC_DS16234,BMG_DS062446,,,,,,,,,C4310630,,617297,MONDO:0015008,"amelogenesis imperfecta, type 1J",
+BMGC_DS16235,BMG_DS062447,,"EPIDERMOLYSIS BULLOSA SIMPLEX 6, GENERALIZED INTERMEDIATE, WITH OR WITHOUT CARDIOMYOPATHY",,,,,,,C4310631,,617294,MONDO:0015006,"epidermolysis bullosa simplex 6, generalized, with scarring and hair loss",
+BMGC_DS16236,BMG_DS062448,,"EPILEPSY, EARLY-ONSET, 1, VITAMIN B6-DEPENDENT",,,,,DOID:0080769,early-onset vitamin B6-dependent epilepsy 1,C4310632,,617290;604436,MONDO:0015005,"epilepsy, early-onset, vitamin B6-dependent",
+BMGC_DS16237,BMG_DS062449,1281844004,Dystonia 28,,,,,DOID:0060936,"dystonia 28, childhood-onset",C4310633,,617284,MONDO:0015004,"dystonia 28, childhood-onset",Dystonia 28 | DYT28 - dystonia 28 | Dystonia 28 (disorder) | KMT2B-related dystonia | Lysine methyltransferase 2B-related dystonia
+BMGC_DS16238,BMG_DS062450,1236805005,MEPAN syndrome,,,,,,,C4310634,,617282,MONDO:0015003,"dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities","Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome (disorder) | MEPAN syndrome | Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome | DYT29 - dystonia 29 | Autosomal recessive childhood-onset dystonia DYT29 type | Childhood-onset generalized dystonia, optic atrophy syndrome | Childhood-onset generalised dystonia, optic atrophy syndrome"
+BMGC_DS16239,BMG_DS062451,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 49,,,,,DOID:0080441,developmental and epileptic encephalopathy 49,C4310635,,617281;617278,MONDO:0015002,"developmental and epileptic encephalopathy, 49",
+BMGC_DS16240,BMG_DS062452,,"ATRIAL FIBRILLATION, FAMILIAL, 18",,,,,,,C4310636,,617280;160770,MONDO:0015001,"atrial fibrillation, familial, 18",
+BMGC_DS16241,BMG_DS062453,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 48,,,,,DOID:0080448,developmental and epileptic encephalopathy 48,C4310637,,617276;602166,MONDO:0015000,"developmental and epileptic encephalopathy, 48",
+BMGC_DS16242,BMG_DS062454,,,,,,,,,C4310638,,617275,MONDO:0014999,"tooth agenesis, selective, 9",
+BMGC_DS16243,BMG_DS062455,,"GLAUCOMA 3, PRIMARY CONGENITAL, E",,,,,,,C4310639,,600221;617272,MONDO:0014998,"glaucoma 3, primary congenital, E",
+BMGC_DS16244,BMG_DS062456,,NEPHRONOPHTHISIS 20,,,,,DOID:0111127,nephronophthisis 20,C4310640,,616786;617271,MONDO:0014997,nephronophthisis 20,
+BMGC_DS16245,BMG_DS062457,,,,,,,,,C4310641,,617270,MONDO:0014996,"intellectual disability, autosomal recessive 58",
+BMGC_DS16246,BMG_DS062458,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE",,,,,,,C4310643,,617245;617268,MONDO:0014995,"neurodevelopmental disorder with hypotonia, seizures, and absent language",
+BMGC_DS16247,BMG_DS062459,,"GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES",,,,,,,C4310644,,617260,MONDO:0014994,"global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies",
+BMGC_DS16248,BMG_DS062460,,"MYOPATHY, MYOFIBRILLAR, 8",,,,,DOID:0080308,myofibrillar myopathy 8,C4310645,,617220;617258,MONDO:0014993,myofibrillar myopathy 8,
+BMGC_DS16249,BMG_DS062461,,LISSENCEPHALY 8,,,,,DOID:0112233,lissencephaly 8,C4310646,,617255;617218,MONDO:0014992,lissencephaly 8,
+BMGC_DS16250,BMG_DS062462,,SECKEL SYNDROME 10,,,,,DOID:0070008,Seckel syndrome 10,C4310647,,617253;617246,MONDO:0014991,Seckel syndrome 10,
+BMGC_DS16251,BMG_DS062463,,UNCOMBABLE HAIR SYNDROME 3,,,,,,,C4310648,,617252;190370,MONDO:0014990,uncombable hair syndrome 3,
+BMGC_DS16252,BMG_DS062464,,UNCOMBABLE HAIR SYNDROME 2,,,,,,,C4310649,,617251;600238,MONDO:0014989,uncombable hair syndrome 2,
+BMGC_DS16253,BMG_DS062465,,"3-METHYLGLUTACONIC ACIDURIA, TYPE VIII",,,,,DOID:0070000,3-methylglutaconic aciduria type 8,C4310650,,617248,MONDO:0044723,3-methylglutaconic aciduria type 8,
+BMGC_DS16254,BMG_DS062466,,"FANCONI ANEMIA, COMPLEMENTATION GROUP U",,,,,DOID:0111085,Fanconi anemia complementation group U,C4310651,,617247;600375,MONDO:0014987,Fanconi anemia complementation group U,
+BMGC_DS16255,BMG_DS062467,,"FANCONI ANEMIA, COMPLEMENTATION GROUP V",,,,,DOID:0111080,Fanconi anemia complementation group V,C4310652,,617243;604094,MONDO:0014985,Fanconi anemia complementation group V,
+BMGC_DS16256,BMG_DS062468,,"LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME",,,,,,,C4310653,,617241;608243,MONDO:0014984,"lung disease, immunodeficiency, and chromosome breakage syndrome;",
+BMGC_DS16257,BMG_DS062469,,"MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC",,,,,DOID:0110672,congenital myasthenic syndrome 21,C4310654,,617239;600336,MONDO:0014983,congenital myasthenic syndrome 21,
+BMGC_DS16258,BMG_DS062470,,"MYOPIA 25, AUTOSOMAL DOMINANT",,,,,,,C4310655,,617238;600608,MONDO:0014982,"myopia 25, autosomal dominant",
+BMGC_DS16259,BMG_DS062471,,IMMUNODEFICIENCY 49,,,,,DOID:0111979,immunodeficiency 49,C4310656,,617237;606558,MONDO:0014981,immunodeficiency 49,
+BMGC_DS16260,BMG_DS062472,,"MYOCLONUS, INTRACTABLE, NEONATAL",,,,,,,C4310658,,617235;602821,MONDO:0014979,"myoclonus, intractable, neonatal",
+BMGC_DS16261,BMG_DS062473,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 16,,,,,,,C4310659,,617234;610363,,,
+BMGC_DS16262,BMG_DS062474,1172703004,POGLUT1-related limb girdle muscular dystrophy R21,,,,,,,C4310660,,617232,MONDO:0014977,autosomal recessive limb-girdle muscular dystrophy type 2R1,POGLUT1-related limb girdle muscular dystrophy R21 | Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 (disorder) | Limb girdle muscular dystrophy type 2Z | Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 | Autosomal recessive limb girdle muscular dystrophy type 2Z
+BMGC_DS16263,BMG_DS062475,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31,,,,,DOID:0111488,combined oxidative phosphorylation deficiency 31,C4310661,,617228;602241,MONDO:0014976,lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome,
+BMGC_DS16264,BMG_DS062476,,"SUDDEN CARDIAC FAILURE, ALCOHOL-INDUCED",,,,,,,C4310663,,617223;609988,MONDO:0014974,"sudden cardiac failure, alcohol-induced",
+BMGC_DS16265,BMG_DS062477,,"SUDDEN CARDIAC FAILURE, INFANTILE",,,,,,,C4310664,,617222;609988,MONDO:0014973,"sudden cardiac failure, infantile",
+BMGC_DS16266,BMG_DS062478,,"AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6",,,,,DOID:0080960,amelogenesis imperfecta type 2A6,C4310665,,601404;617217,MONDO:0014971,"amelogenesis imperfecta, hypomaturation type, IIa6",
+BMGC_DS16267,BMG_DS062479,,SPERMATOGENIC FAILURE 17,,,,,DOID:0070174,spermatogenic failure 17,C4310666,,608075;617214,MONDO:0014970,spermatogenic failure 17,
+BMGC_DS16268,BMG_DS062480,,"ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY",,,,,,,C4310667,,604934;617207,MONDO:0014968,"encephalopathy, progressive, with amyotrophy and optic atrophy",
+BMGC_DS16269,BMG_DS062481,,"HETEROTAXY, VISCERAL, 8, AUTOSOMAL",,,,,,,C4310668,,609721;617205,MONDO:0014967,"heterotaxy, visceral, 8, autosomal",
+BMGC_DS16270,BMG_DS062482,,PERIVENTRICULAR NODULAR HETEROTOPIA 7,,,,,,,C4310669,,606384;617201,MONDO:0014966,periventricular nodular heterotopia 7,
+BMGC_DS16271,BMG_DS062483,,LETHAL CONGENITAL CONTRACTURE SYNDROME 11,,,,,,,C4310670,,617194;608603,MONDO:0014965,lethal congenital contracture syndrome 11,
+BMGC_DS16272,BMG_DS062484,,SHASHI-PENA SYNDROME,,,,,,,C4310672,,612991;617190,MONDO:0014963,Shashi-Pena syndrome,
+BMGC_DS16273,BMG_DS062485,,,,,,,,,C4310673,,617188,MONDO:0014962,"intellectual disability, autosomal recessive 57",
+BMGC_DS16274,BMG_DS062486,,SPERMATOGENIC FAILURE 16,,,,,DOID:0070184,spermatogenic failure 16,C4310674,,617187;613942,MONDO:0014961,spermatogenic failure 16,
+BMGC_DS16275,BMG_DS062487,,"ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY",,,,,,,C4310675,,617186;608862,MONDO:0020781,"encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1",
+BMGC_DS16276,BMG_DS062488,,"MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT",,,,,DOID:0080130,mitochondrial DNA depletion syndrome 12a,C4310676,,103220;617184,MONDO:0014959,"mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant",
+BMGC_DS16277,BMG_DS062489,1172586007,"Ocular anomalies, axonal neuropathy, developmental delay syndrome",,,,,,,C4310677,,617183,MONDO:0014958,Harel-Yoon syndrome,"Ocular anomalies, axonal neuropathy, developmental delay syndrome | Harel Yoon syndrome | Ocular anomalies, axonal neuropathy, developmental delay syndrome (disorder)"
+BMGC_DS16278,BMG_DS062490,,"LODDER-MERLA SYNDROME, TYPE 2, WITH DEVELOPMENTAL DELAY AND WITH OR WITHOUT CARDIAC ARRHYTHMIA",,,,,,,C4310678,,617182;604447,MONDO:0014957,language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia,
+BMGC_DS16279,BMG_DS062491,,CHITAYAT SYNDROME,,,,,,,C4310679,,617180;611888,MONDO:0014956,Chitayat syndrome,
+BMGC_DS16280,BMG_DS062492,,RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES,,,,,,,C4310680,,617175;607867,MONDO:0014955,RCBTB1-related retinopathy,
+BMGC_DS16281,BMG_DS062493,,"EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2",,,,,DOID:0080987,Ehlers-Danlos syndrome periodontal type 2,C4310681,,617174;120580,MONDO:0014954,"Ehlers-Danlos syndrome, periodontal type 2",
+BMGC_DS16282,BMG_DS062494,,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND IMPAIRED EXPRESSIVE LANGUAGE AND WITH OR WITHOUT SEIZURES,,,,,,,C4310683,,617171;602635,MONDO:0014952,intellectual disability-epilepsy-extrapyramidal syndrome,
+BMGC_DS16283,BMG_DS062495,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 74",,,,,DOID:0081218;DOID:0112104,Sotos syndrome 3 | autosomal recessive intellectual developmental disorder 74,C4310684,,617169;612034,MONDO:0014951,"intellectual developmental disorder, autosomal recessive 74",
+BMGC_DS16284,BMG_DS062496,,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47",,,,,DOID:0080425,developmental and epileptic encephalopathy 47,C4310685,,617166,MONDO:0014949,"developmental and epileptic encephalopathy, 47",
+BMGC_DS16285,BMG_DS062497,,SHORT STATURE-MICROGNATHIA SYNDROME,,,,,,,C4310686,,617164;600820,MONDO:0014948,"short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay",
+BMGC_DS16286,BMG_DS062498,,,,,,,,,C4310687,,617162,MONDO:0014947,"developmental and epileptic encephalopathy, 46",
+BMGC_DS16287,BMG_DS062499,,SIFRIM-HITZ-WEISS SYNDROME,,,,,DOID:0070529,Sifrim-Hitz-Weiss syndrome,C4310688,,617159;603277,MONDO:0014946,Sifrim-Hitz-Weiss syndrome,
+BMGC_DS16288,BMG_DS062500,,"SHORT STATURE, BRACHYDACTYLY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES",,,,,,,C4310689,,610087;617157,MONDO:0014944,short stature-brachydactyly-obesity-global developmental delay syndrome,
+BMGC_DS16289,BMG_DS062501,,MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE),,,,,DOID:0080337,mitochondrial DNA depletion syndrome 15,C4310690,,600438;617156,MONDO:0014943,mitochondrial DNA depletion syndrome 15 (hepatocerebral type),
+BMGC_DS16290,BMG_DS062502,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 45,,,,,DOID:0080428,developmental and epileptic encephalopathy 45,C4310691,,617153;137190,MONDO:0014942,"developmental and epileptic encephalopathy, 45",
+BMGC_DS16291,BMG_DS062503,,"ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH",,,,,,,C4310692,,617146;613629,MONDO:0014941,"arthrogryposis, distal, with impaired proprioception and touch",
+BMGC_DS16292,BMG_DS062504,,"NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET",,,,,DOID:0081364,"neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset",C4310693,,617145;601530,MONDO:0014940,"neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset",
+BMGC_DS16293,BMG_DS062505,,"MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC",,,,,DOID:0110661,congenital myasthenic syndrome 20,C4310694,,608761;617143,MONDO:0014939,congenital myasthenic syndrome 20,
+BMGC_DS16294,BMG_DS062506,,,,,,,,,C4310695,,617142,MONDO:0014938,aniridia 3,
+BMGC_DS16295,BMG_DS062507,1169355000,"Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome",,,,,DOID:0060953,ZTTK syndrome,C4310696,,617140,MONDO:0014936,ZTTK syndrome,"Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome | Zhu Tokita Takenouchi Kim syndrome | ZTTK syndrome | Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome (disorder)"
+BMGC_DS16296,BMG_DS062508,,FRONTOMETAPHYSEAL DYSPLASIA 2,,,,,DOID:0111787,frontometaphyseal dysplasia 2,C4310697,,617137;602614,MONDO:0014935,frontometaphyseal dysplasia 2,
+BMGC_DS16297,BMG_DS062509,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24",,,,,DOID:0111615,autosomal recessive spinocerebellar ataxia 24,C4310699,,617133;610552,MONDO:0014934,"spinocerebellar ataxia, autosomal recessive 24",
+BMGC_DS16298,BMG_DS062510,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 44,,,,,DOID:0080424,developmental and epileptic encephalopathy 44,C4310700,,617132;610552,MONDO:0014933,"developmental and epileptic encephalopathy, 44",
+BMGC_DS16299,BMG_DS062511,,OROFACIODIGITAL SYNDROME XV,,,,,,,C4310701,,617112;617127,MONDO:0014932,orofaciodigital syndrome XV,
+BMGC_DS16300,BMG_DS062512,,ALAZAMI-YUAN SYNDROME,,,,,,,C4310702,,602955;617126,MONDO:0014931,Alazami-Yuan syndrome,
+BMGC_DS16301,BMG_DS062513,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 56",,,,,DOID:0081217,autosomal recessive intellectual developmental disorder 56,C4310703,,617125;613279,MONDO:0014930,"intellectual disability, autosomal recessive 56",
+BMGC_DS16302,BMG_DS062514,,RETINITIS PIGMENTOSA 76,,,,,,,C4310704,,617123;606822,MONDO:0014929,retinitis pigmentosa 76,
+BMGC_DS16303,BMG_DS062515,,JOUBERT SYNDROME 28,,,,,DOID:0110997,Joubert syndrome 28,C4310705,,617121;609883,MONDO:0014928,Joubert syndrome 28,
+BMGC_DS16304,BMG_DS062516,,JOUBERT SYNDROME 27,,,,,DOID:0110996,Joubert syndrome 27,C4310706,,617120;614144,MONDO:0014927,Joubert syndrome 27,
+BMGC_DS16305,BMG_DS062517,,BARDET-BIEDL SYNDROME 20,,,,,DOID:0081009,Bardet-Biedl syndrome 20,C4310707,,607386;619471,MONDO:0023670,Bardet-Biedl syndrome 20,
+BMGC_DS16306,BMG_DS062518,,"EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3",,,,,DOID:0081423,familial focal epilepsy with variable foci 3,C4310708,,600928;617118,MONDO:0014925,"epilepsy, familial focal, with variable foci 3",
+BMGC_DS16307,BMG_DS062519,,"EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 2",,,,,DOID:0081422,familial focal epilepsy with variable foci 2,C4310709,,617116;607072,MONDO:0014924,"epilepsy, familial focal, with variable foci 2",
+BMGC_DS16308,BMG_DS062520,,PEELING SKIN SYNDROME 5,,,,,DOID:0070524,peeling skin syndrome 5,C4310710,,617115;601697,MONDO:0014923,peeling skin syndrome 5,
+BMGC_DS16309,BMG_DS062521,,"MYOPATHY, MYOFIBRILLAR, 7",,,,,DOID:0080098,myofibrillar myopathy 7,C4310711,,617114;605739,MONDO:0014922,myofibrillar myopathy 7,
+BMGC_DS16310,BMG_DS062522,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 43,,,,,DOID:0080447,developmental and epileptic encephalopathy 43,C4310712,,137192;617113,MONDO:0014921,"developmental and epileptic encephalopathy, 43",
+BMGC_DS16311,BMG_DS062523,1187639002,Martinique crinkled retinal pigment epitheliopathy,,,,,,,C4310713,,617111,MONDO:0014920,patterned macular dystrophy 3,Martinique crinkled retinal pigment epitheliopathy | Martinique crinkled retinal pigment epitheliopathy (disorder) | MCRPE - Martinique crinkled retinal pigment epitheliopathy
+BMGC_DS16312,BMG_DS062524,,,,,,,,,C4310714,,617108,MONDO:0014919,sessile serrated polyposis cancer syndrome,
+BMGC_DS16313,BMG_DS062525,1169359006,"Tall stature, intellectual disability, renal anomalies syndrome",,,,,,,C4310715,,617107,MONDO:0014918,tall stature-intellectual disability-renal anomalies syndrome,"Tall stature, intellectual disability, renal anomalies syndrome | Thauvin Robinet Faivre syndrome | Tall stature, intellectual disability, renal anomalies syndrome (disorder)"
+BMGC_DS16314,BMG_DS062526,,,,,,,,,C4310716,,617106,MONDO:0014917,"developmental and epileptic encephalopathy, 42",
+BMGC_DS16315,BMG_DS062527,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 41,,,,,DOID:0080442,developmental and epileptic encephalopathy 41,C4310717,,600300;617105,MONDO:0014916,"developmental and epileptic encephalopathy, 41",
+BMGC_DS16316,BMG_DS062528,,SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY,,,,,,,C4310718,,617102,MONDO:0014915,short-rib thoracic dysplasia 16 with or without polydactyly,
+BMGC_DS16317,BMG_DS062529,,FAMILIAL ADENOMATOUS POLYPOSIS 4,,,,,DOID:0080412,familial adenomatous polyposis 4,C4310719,,600887;617100,MONDO:0044300,familial adenomatous polyposis 4,
+BMGC_DS16318,BMG_DS062530,,"GROWTH RETARDATION, IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND HEPATOPATHY",,,,,,,C4310720,,600709;617093,MONDO:0014911,"growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy",
+BMGC_DS16319,BMG_DS062531,,"CILIARY DYSKINESIA, PRIMARY, 35",,,,,DOID:0110620,primary ciliary dyskinesia 35,C4310721,,617092;617095,MONDO:0014910,primary ciliary dyskinesia 35,
+BMGC_DS16320,BMG_DS062532,,"CILIARY DYSKINESIA, PRIMARY, 34",,,,,DOID:0110610,primary ciliary dyskinesia 34,C4310722,,617091;610263,MONDO:0014909,primary ciliary dyskinesia 34,
+BMGC_DS16321,BMG_DS062533,,"MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE",,,,,DOID:0070288,primary autosomal recessive microcephaly 17,C4310723,,605629;617090,MONDO:0014908,"microcephaly 17, primary, autosomal recessive",
+BMGC_DS16322,BMG_DS062534,,SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY,,,,,,,C4310724,,617088;617083,MONDO:0014907,short-rib thoracic dysplasia 15 with polydactyly,
+BMGC_DS16323,BMG_DS062535,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B",,,,,DOID:0111557,Charcot-Marie-Tooth disease type 2A2B,C4310725,,617087,MONDO:0014906,"Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;",
+BMGC_DS16324,BMG_DS062536,,ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2,,,,,DOID:0060994,encephalopathy due to defective mitochondrial and peroxisomal fission 2,C4310726,,617086;614785,MONDO:0014905,encephalopathy due to defective mitochondrial and peroxisomal fission 2,
+BMGC_DS16325,BMG_DS062537,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iaa",,,,,DOID:0080553,congenital disorder of glycosylation Iaa,C4310727,,617082;610463,MONDO:0014904,"congenital disorder of glycosylation, type IAA",
+BMGC_DS16326,BMG_DS062538,,"SEIZURES, BENIGN FAMILIAL INFANTILE, 5",,,,,DOID:0081118,benign familial infantile seizures 5,C4310728,,617080;600702,MONDO:0014903,"seizures, benign familial infantile, 5",
+BMGC_DS16327,BMG_DS062539,,,,,,,,,C4310729,,617075,MONDO:0014902,"nasopharyngeal carcinoma, susceptibility to, 3",
+BMGC_DS16328,BMG_DS062540,,"TOOTH AGENESIS, SELECTIVE, 8",,,,,,,C4310730,,617073;601906,MONDO:0014901,"tooth agenesis, selective, 8",
+BMGC_DS16329,BMG_DS062541,,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4",,,,,DOID:0111516,autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4,C4310733,,617070;601465,MONDO:0014899,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4",
+BMGC_DS16330,BMG_DS062542,,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3",,,,,DOID:0111523,autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3,C4310734,,188250;617069,MONDO:0014898,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3",
+BMGC_DS16331,BMG_DS062543,,"PORTAL HYPERTENSION, NONCIRRHOTIC, 1",,,,,,,C4310735,,601465;617068,MONDO:0024193,"portal hypertension, noncirrhotic",
+BMGC_DS16332,BMG_DS062544,1172688004,"Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome",,,,,,,C4310736,,617066,MONDO:0014896,congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome,"Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome (disorder) | Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome | Congenital muscular dystrophy Davignon Chauveau type"
+BMGC_DS16333,BMG_DS062545,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 40,,,,,DOID:0080427,developmental and epileptic encephalopathy 40,C4310737,,617064;617065,MONDO:0014895,"developmental and epileptic encephalopathy, 40",
+BMGC_DS16334,BMG_DS062546,,MEIER-GORLIN SYNDROME 7,,,,,DOID:0080518,Meier-Gorlin syndrome 7,C4310738,,603465;617063,MONDO:0014894,Meier-Gorlin syndrome 7,
+BMGC_DS16335,BMG_DS062547,,OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME,,,,,,,C4310739,,115440;617062,MONDO:0014893,Okur-Chung neurodevelopmental syndrome,
+BMGC_DS16336,BMG_DS062548,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 44, WITH MICROCEPHALY",,,,,DOID:0070074,autosomal dominant intellectual developmental disorder 44,C4310740,,601893;617061,MONDO:0014892,micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome,
+BMGC_DS16337,BMG_DS062549,,"TUBULOINTERSTITIAL KIDNEY DISEASE, AUTOSOMAL DOMINANT, 5",,,,,,,C4310741,,609213;617056,MONDO:0014891,"hyperuricemic nephropathy, familial juvenile type 4",
+BMGC_DS16338,BMG_DS062550,,PERCHING SYNDROME,,,,,DOID:0080331,cold-induced sweating syndrome 3,C4310742,,611119;617055,MONDO:0014890,PERCHING syndrome,
+BMGC_DS16339,BMG_DS062551,1172584005,Childhood-onset basal ganglia degeneration syndrome,,,,,,,C4310743,,617054,MONDO:0014889,"striatonigral degeneration, childhood-onset",Childhood-onset basal ganglia degeneration syndrome | Childhood-onset basal ganglia degeneration syndrome (disorder) | Lenk Ploski syndrome
+BMGC_DS16340,BMG_DS062552,,BONE MARROW FAILURE SYNDROME 3,,,,,,,C4310744,,617052;617048,MONDO:0014887,bone marrow failure syndrome 3,
+BMGC_DS16341,BMG_DS062553,,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND GRAY SCLERAE,,,,,,,C4310745,,617051;616283,MONDO:0014886,severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome,
+BMGC_DS16342,BMG_DS062554,,HERMANSKY-PUDLAK SYNDROME 10,,,,,,,C4310746,,617050;607246,MONDO:0014885,Hermansky-Pudlak syndrome 10,
+BMGC_DS16343,BMG_DS062555,,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5",,,,,DOID:0070225,progressive familial intrahepatic cholestasis 5,C4310747,,603826;617049,MONDO:0014884,"cholestasis, progressive familial intrahepatic, 5",
+BMGC_DS16344,BMG_DS062556,,"CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 5",,,,,DOID:0110327,hypertrophic cardiomyopathy 26,C4310748,,617047;102565,MONDO:0800371,"cardiomyopathy, familial restrictive, 5",
+BMGC_DS16345,BMG_DS062557,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26",,,,,DOID:0110327,hypertrophic cardiomyopathy 26,C4310749,,617047;102565,MONDO:0014883,hypertrophic cardiomyopathy 26,
+BMGC_DS16346,BMG_DS062558,,DUANE RETRACTION SYNDROME 3 WITH OR WITHOUT DEAFNESS,,,,,,,C4310752,,617041,MONDO:0014880,Duane retraction syndrome 3 with or without deafness,
+BMGC_DS16347,BMG_DS062559,,,,,,,,,C4310753,,617039,MONDO:0024266,patent ductus arteriosus 3,
+BMGC_DS16348,BMG_DS062560,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 54",,,,,DOID:0081216,autosomal recessive intellectual developmental disorder 54,C4310755,,617028;610005,MONDO:0014876,"intellectual disability, autosomal recessive 54",
+BMGC_DS16349,BMG_DS062561,,"HYPERALDOSTERONISM, FAMILIAL, TYPE IV",,,,,,,C4310756,,617027;607904,MONDO:0014875,"hyperaldosteronism, familial, type IV",
+BMGC_DS16350,BMG_DS062562,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 2F",,,,,DOID:0112329,pontocerebellar hypoplasia type 2F,C4310757,,617026;608756,MONDO:0014874,"pontocerebellar hypoplasia, type 2F",
+BMGC_DS16351,BMG_DS062563,,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H",,,,,DOID:0110866,congenital stationary night blindness 1H,C4310758,,617024;139130,MONDO:0014872,congenital stationary night blindness 1H,
+BMGC_DS16352,BMG_DS062564,,RETINITIS PIGMENTOSA 75,,,,,,,C4310759,,617023;615900,MONDO:0014871,retinitis pigmentosa 75,
+BMGC_DS16353,BMG_DS062565,1237349008,"Hydrops, lactic acidosis, sideroblastic anemia, multisystemic failure syndrome",,,,,,,C4310761,,617021,MONDO:0014869,hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome,"Hydrops, lactic acidosis, sideroblastic anemia, multisystemic failure syndrome (disorder) | Hydrops, lactic acidosis, sideroblastic anaemia, multisystemic failure syndrome | Hydrops, lactic acidosis, sideroblastic anemia, multisystemic failure syndrome"
+BMGC_DS16354,BMG_DS062566,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 38,,,,,DOID:0080417,developmental and epileptic encephalopathy 38,C4310762,,617020;611647,MONDO:0014868,"developmental and epileptic encephalopathy, 38",
+BMGC_DS16355,BMG_DS062567,,SPINOCEREBELLAR ATAXIA 43,,,,,DOID:0111745,cerebellar ataxia type 43,C4310763,,617018;120520,MONDO:0014867,spinocerebellar ataxia 43,
+BMGC_DS16356,BMG_DS062568,,"NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE",,,,,DOID:0112129,severe congenital neutropenia 7,C4310764,,617014;138971,MONDO:0014865,autosomal recessive severe congenital neutropenia due to CSF3R deficiency,
+BMGC_DS16357,BMG_DS062569,768554008,Hypermanganesemia with dystonia 2,,,,,,,C4310765,,617013,MONDO:0014864,hypermanganesemia with dystonia 2,HMNDYT2 - hypermanganesemia with dystonia 2 | Hypermanganesemia with dystonia 2 (disorder) | Hypermanganesemia with dystonia 2
+BMGC_DS16358,BMG_DS062570,,"MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION",,,,,,,C4310766,,605109;617011,MONDO:0014863,"macrocephaly, dysmorphic facies, and psychomotor retardation",
+BMGC_DS16359,BMG_DS062571,,"CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3",,,,,DOID:0081361,spastic quadriplegic cerebral palsy 3,C4310767,,617008;601568,MONDO:0014862,"cerebral palsy, spastic quadriplegic, 3",
+BMGC_DS16360,BMG_DS062572,,"AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2",,,,,,,C4310768,,617006;176947,MONDO:0014861,"autoimmune disease, multisystem, infantile-onset, 2",
+BMGC_DS16361,BMG_DS062573,,POLYCYSTIC LIVER DISEASE 2 WITH OR WITHOUT KIDNEY CYSTS,,,,,DOID:0060975,polycystic liver disease 2,C4310769,,617004,MONDO:0014860,polycystic liver disease 2,
+BMGC_DS16362,BMG_DS062574,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 37,,,,,DOID:0080435,developmental and epileptic encephalopathy 37,C4310770,,616981;604574,MONDO:0014859,"developmental and epileptic encephalopathy, 37",
+BMGC_DS16363,BMG_DS062575,,,,,,,,,C4310771,,616977,MONDO:0014858,"intellectual disability, autosomal dominant 43",
+BMGC_DS16364,BMG_DS062576,,"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART",,,,,,,C4310772,,616975,MONDO:0014857,"neurodevelopmental disorder with or without anomalies of the brain, eye, or heart",
+BMGC_DS16365,BMG_DS062577,,,,,,,,,C4310774,,616973,MONDO:0014855,"intellectual disability, autosomal dominant 42",
+BMGC_DS16366,BMG_DS062578,,"DEAFNESS, AUTOSOMAL DOMINANT 70",,,,,,,C4310775,,616968;116945,MONDO:0014853,autosomal dominant nonsyndromic hearing loss 70,
+BMGC_DS16367,BMG_DS062579,,RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS,,,,,,,C4310776,,616959;612907,MONDO:0014850,retinitis pigmentosa and erythrocytic microcytosis,
+BMGC_DS16368,BMG_DS062580,1172626003,"TELO2-related intellectual disability, neurodevelopmental disorder",,,,,,,C4310778,,616954,MONDO:0014848,TELO2-related intellectual disability-neurodevelopmental disorder,"Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (disorder) | TELO2-related intellectual disability, neurodevelopmental disorder | Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder | You Hoover Fong syndrome"
+BMGC_DS16369,BMG_DS062581,,SPERMATOGENIC FAILURE 15,,,,,DOID:0070172,spermatogenic failure 15,C4310779,,616950;611486,MONDO:0014847,spermatogenic failure 15,
+BMGC_DS16370,BMG_DS062582,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22",,,,,DOID:0111614,autosomal recessive spinocerebellar ataxia 22,C4310781,,614884;616948,MONDO:0014845,"spinocerebellar ataxia, autosomal recessive 22",
+BMGC_DS16371,BMG_DS062583,,PREMATURE OVARIAN FAILURE 12,,,,,DOID:0080869,primary ovarian insufficiency 12,C4310782,,611486;616947,MONDO:0014844,premature ovarian failure 12,
+BMGC_DS16372,BMG_DS062584,,PREMATURE OVARIAN FAILURE 11,,,,,DOID:0080868,primary ovarian insufficiency 11,C4310783,,609413;616946,MONDO:0014843,premature ovarian failure 11,
+BMGC_DS16373,BMG_DS062585,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 41",,,,,DOID:0070071,autosomal dominant intellectual developmental disorder 41,C4310784,,608628;616944,MONDO:0014842,"intellectual disability, autosomal dominant 41",
+BMGC_DS16374,BMG_DS062586,,"TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE",,,,,DOID:0111872,nonphotosensitive trichothiodystrophy 6,C4310785,,189964;616943,MONDO:0014841,"trichothiodystrophy 6, nonphotosensitive",
+BMGC_DS16375,BMG_DS062587,,"AGAMMAGLOBULINEMIA 8A, AUTOSOMAL DOMINANT",,,,,DOID:0081140,agammaglobulinemia 8A,C4310786,,616941;147141,MONDO:0014840,"agammaglobulinemia 8, autosomal dominant",
+BMGC_DS16376,BMG_DS062588,,"CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION",,,,,,,C4310787,,607468;616939,MONDO:0014839,"chorea, childhood-onset, with psychomotor retardation",
+BMGC_DS16377,BMG_DS062589,,COFFIN-SIRIS SYNDROME 5,,,,,DOID:0112368,Coffin-Siris syndrome 5,C4310788,,616938;603111,MONDO:0014838,Coffin-Siris syndrome 5,
+BMGC_DS16378,BMG_DS062590,,THROMBOCYTOPENIA 6,,,,,,,C4310789,,616937;190090,MONDO:0014837,thrombocytopenia 6,
+BMGC_DS16379,BMG_DS062591,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC",,,,,DOID:0110180,Charcot-Marie-Tooth disease axonal type 2CC,C4310790,,616924;162230,MONDO:0014836,Charcot-Marie-Tooth disease axonal type 2CC,
+BMGC_DS16380,BMG_DS062592,,"STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2",,,,,DOID:0060998,striatal degeneration 2,C4310791,,616922;610652,MONDO:0014835,"striatal degeneration, autosomal dominant 2",
+BMGC_DS16381,BMG_DS062593,,HEART AND BRAIN MALFORMATION SYNDROME,,,,,,,C4310793,,616920;613176,MONDO:0014833,heart and brain malformation syndrome,
+BMGC_DS16382,BMG_DS062594,,"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPOTONIA, SEIZURES, AND CEREBELLAR ATROPHY",,,,,,,C4310794,,616917;616918,MONDO:0014832,"intellectual disability, autosomal recessive 53",
+BMGC_DS16383,BMG_DS062595,,MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME,,,,,,,C4310796,,134797;616914,MONDO:0014831,progeroid and marfanoid aspect-lipodystrophy syndrome,
+BMGC_DS16384,BMG_DS062596,,"BLEEDING DISORDER, PLATELET-TYPE, 20",,,,,DOID:0111055,platelet-type bleeding disorder 20,C4310797,,614958;616913,MONDO:0014830,platelet-type bleeding disorder 20,
+BMGC_DS16385,BMG_DS062597,,IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4,,,,,,,C4310798,,616911;603946,MONDO:0014829,immunodeficiency-centromeric instability-facial anomalies syndrome 4,
+BMGC_DS16386,BMG_DS062598,,IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3,,,,,,,C4310799,,616910;609937,MONDO:0014828,immunodeficiency-centromeric instability-facial anomalies syndrome 3,
+BMGC_DS16387,BMG_DS062599,1217229007,"Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome",,,,,,,C4310801,,,MONDO:0031632,"developmental delay with short stature, dysmorphic facial features, and sparse hair","Developmental delay, short stature, dysmorphic features, sparse hair syndrome | Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome (disorder) | Loucks Innes syndrome | Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome"
+BMGC_DS16388,BMG_DS062600,,"PARKINSON DISEASE 19B, EARLY-ONSET",,,,,,,C4310802,,608375;615528,MONDO:0800369,"parkinson disease 19B, early-onset",
+BMGC_DS16389,BMG_DS062601,,IMMUNODEFICIENCY 51,,,,,DOID:0111996,immunodeficiency 51,C4310803,,605461;613953,MONDO:0013500,immunodeficiency 51,
+BMGC_DS16390,BMG_DS062602,1187122000,Witteveen Kolk syndrome,,,,,,,C4310804,,,MONDO:0044700,SIN3A-related intellectual disability syndrome due to a point mutation,WITKOS - Witteveen Kolk syndrome | Witteveen Kolk syndrome | Witteveen Kolk syndrome (disorder) | SIN3A-related intellectual disability syndrome | SIN3A (Switch-insensitive 3 transcription regulator family member A)-related intellectual disability syndrome
+BMGC_DS16391,BMG_DS062603,,"BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS",,,,,,,C4310805,,613090,MONDO:0000909,Bartter disease type 4B,
+BMGC_DS16392,BMG_DS062604,,CATARACT 47,,,,,DOID:0070353,cataract 47,C4310806,,612018,MONDO:0012786,juvenile cataract-microcornea-renal glucosuria syndrome,
+BMGC_DS16393,BMG_DS062605,,BRACHYDACTYLY-SYNDACTYLY-OLIGODACTYLY SYNDROME,,,,,,,C4310807,,142989;610713,MONDO:0800344,brachydactyly-syndactyly-oligodactyly syndrome,
+BMGC_DS16394,BMG_DS062606,,"STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 1",,,,,,,C4310808,,603390;609161,MONDO:0012205,autosomal dominant striatal neurodegeneration type 1,
+BMGC_DS16395,BMG_DS062607,,ANTERIOR SEGMENT DYSGENESIS 5,,,,,DOID:0080610,anterior segment dysgenesis 5,C4310809,,604229,,,
+BMGC_DS16396,BMG_DS062608,,"MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS",,,,,DOID:0111859,"midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis",C4310810,,300195;300990,MONDO:0010516,"midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis",
+BMGC_DS16397,BMG_DS062609,,MEESTER-LOEYS SYNDROME,,,,,DOID:0111861,Meester-Loeys syndrome,C4310811,,301870;300989,MONDO:0010515,Meester-Loeys syndrome,
+BMGC_DS16398,BMG_DS062610,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BAIN TYPE",,,,,DOID:0070538,syndromic X-linked intellectual developmental disorder bain type,C4310814,,300610;300986,MONDO:0010512,"intellectual disability, X-linked, syndromic, Bain type",
+BMGC_DS16399,BMG_DS062611,,"VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF, X-LINKED",,,,,DOID:0111863,X-linked congenital bilateral absence of vas deferens,C4310815,,300572;300985,MONDO:0010511,"vas deferens, congenital bilateral aplasia of, X-linked",
+BMGC_DS16400,BMG_DS062612,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 105",,,,,DOID:0112036,non-syndromic X-linked intellectual disability 105,C4310816,,300984;300975,MONDO:0010510,"intellectual disability, X-linked 105",
+BMGC_DS16401,BMG_DS062613,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 104",,,,,DOID:0112018,non-syndromic X-linked intellectual disability 104,C4310817,,300983;300838,MONDO:0010509,"intellectual disability, X-linked 104",
+BMGC_DS16402,BMG_DS062614,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 103",,,,,DOID:0112020,non-syndromic X-linked intellectual disability 103,C4310818,,300980;300982,MONDO:0010508,"intellectual disability, X-linked 103",
+BMGC_DS16403,BMG_DS062615,,IMMUNODEFICIENCY 47,,,,,DOID:0112002,immunodeficiency 47,C4310819,,300197;300972,MONDO:0010504,immunodeficiency 47,
+BMGC_DS16404,BMG_DS062616,,"BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT",,,,,,,C4310820,,300971;300470,MONDO:0010503,Bartter disease type 5,
+BMGC_DS16405,BMG_DS062617,,LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY,,,,,,,C4310822,,255100;610595,MONDO:0009703,myopathy with abnormal lipid metabolism,
+BMGC_DS16406,BMG_DS062618,,"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, AND MILD PALMOPLANTAR KERATODERMA WITH OR WITHOUT WOOLLY HAIR",,,,,,,C4310824,,610476,,,
+BMGC_DS16407,BMG_DS062619,,,,,,,,,C4310831,,,MONDO:0800413,"antisocial behavior, susceptibility to",
+BMGC_DS16408,BMG_DS062620,,,,,,,,,C4310833,,617101,MONDO:0014914,Dias-Logan syndrome,
+BMGC_DS16409,BMG_DS062621,,"ALACRIMA, CONGENITAL, AUTOSOMAL DOMINANT",,,,,,,C4310836,,103420,MONDO:0007075,"alacrima, congenital, autosomal dominant",
+BMGC_DS16410,BMG_DS062622,,"SANDHOFF DISEASE, CHRONIC",,,,,,,C4310842,,606873,,,
+BMGC_DS16411,BMG_DS062627,,DUANE RETRACTION SYNDROME 3,,,,,,,C4310873,,608968,,,
+BMGC_DS16412,BMG_DS062636,,"BETA-HEXOSAMINIDASE A, PSEUDODEFICIENCY OF",,,,,,,C4310892,,606869,,,
+BMGC_DS16413,BMG_DS062637,,"GM2-GANGLIOSIDOSIS, ADULT-ONSET",,,,,,,C4310893,,606869,,,
+BMGC_DS16414,BMG_DS062647,,"ANTERIOR SEGMENT DYSGENESIS 1, MULTIPLE SUBTYPES",,,,,,,C4310917,,602669,,,
+BMGC_DS16415,BMG_DS062657,,GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE,,,,,,,C4310943,,601019;617301,MONDO:0015010,atypical glycine encephalopathy,
+BMGC_DS16416,BMG_DS062663,,"BETA-THALASSEMIA, ASHKENAZI JEWISH TYPE",,,,,,,C4310972,,141900,,,
+BMGC_DS16417,BMG_DS062664,,"BETA-THALASSEMIA INTERMEDIA, DOMINANT",,,,,,,C4310973,,141900,,,
+BMGC_DS16418,BMG_DS062668,,"CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL",,,,,,,C4311046,,617219,MONDO:0014972,"chromosome 19q13.11 deletion syndrome, proximal",
+BMGC_DS16419,BMG_DS062669,,"CHROMOSOME 11p13 DELETION SYNDROME, DISTAL",,,,,,,C4311047,,616902,MONDO:0014825,"chromosome 11p13 deletion syndrome, distal",
+BMGC_DS16420,BMG_DS062670,,"CHROMOSOME 19q13.11 DELETION SYNDROME, DISTAL",,,,,,,C4311048,,613026,MONDO:0700107,"chromosome 19q13.11 deletion syndrome, distal",
+BMGC_DS16421,BMG_DS062671,,CHROMOSOME Xq25 DUPLICATION SYNDROME,,,,,,,C4311049,,300979,MONDO:0010507,Xq25 microduplication syndrome,
+BMGC_DS16422,BMG_DS062677,,Nocturnal frontal lobe epilepsy,,,,,,,C4313718,,MTHU056122,MONDO:0000030,sleep-related hypermotor epilepsy,
+BMGC_DS16423,BMG_DS062701,,,,,,,,,C4315392,,,MONDO:0019677,brachydactyly type E,
+BMGC_DS16424,BMG_DS062793,,"Kenny-Caffey syndrome, type 2",,,,,,,C4316787,C537020,127000,MONDO:0007478,autosomal dominant Kenny-Caffey syndrome,
+BMGC_DS16425,BMG_DS062794,,,,,,,,,C4316789,,,MONDO:0027767,partial lipodystrophy,
+BMGC_DS16426,BMG_DS062796,,Entamoeba histolytica Infection,Entamoebiasis,,,,,,C4316791,D004749,,,,
+BMGC_DS16427,BMG_DS062799,,Writer's Cramp,Dystonic Disorders,,,,,,C4316810,D020821,,,,
+BMGC_DS16428,BMG_DS062800,,Fibrinogen Deficiency,Afibrinogenemia,,,,,,C4316812,D000347,,,,
+BMGC_DS16429,BMG_DS062802,,,,,,,,,C4316870,,,MONDO:0005328,eye disorder,
+BMGC_DS16430,BMG_DS062806,190681003;111398009;367374009,Cystinosis,Cystinosis,,,E72.04,,,C4316899,D003554,,MONDO:0016239,cystinosis,Cystinosis | Cystine disease | Cystine storage disease | Cystine diathesis | Cystinosis (disorder) | Cystinosis | Cystinosis (disorder) | Lignac-Fanconi syndrome | Cystinosis (disorder) | Cystinosis
+BMGC_DS16431,BMG_DS062807,,Absence Seizures,Seizures,,,,,,C4316903,D012640,,,,
+BMGC_DS16432,BMG_DS062811,,Primary Hypothyroidism,Hypothyroidism,,,,,,C4316995,D007037,,,,
+BMGC_DS16433,BMG_DS062812,,Diverticular Diseases,Diverticular Diseases,,,,,,C4317009,D000076385,,,,
+BMGC_DS16434,BMG_DS062813,439143004,Simpson-Golabi-Behmel syndrome,,,,,,,C4317043,,,MONDO:0010731,Simpson-Golabi-Behmel syndrome,Simpson-Golabi-Behmel syndrome (disorder) | Bulldog syndrome | Simpson-Golabi-Behmel syndrome
+BMGC_DS16435,BMG_DS062816,,,,,,,,,C4317107,,,MONDO:0003240,thyroid gland disorder,
+BMGC_DS16436,BMG_DS062817,,Epileptic Seizures,Seizures,,,,,,C4317109,D012640,,,,
+BMGC_DS16437,BMG_DS062819,,Polynesian Bronchiectasis,Kartagener Syndrome,,,,DOID:0050144,Kartagener syndrome,C4317124,D007619,,,,
+BMGC_DS16438,BMG_DS062820,418279001;56550003;238127001,Niacin deficiency,,,,,,,C4317126,,,,,Niacin deficiency (disorder) | Niacin deficiency | Nicotinamide deficiency | Nicotinic acid deficiency | Vitamin B3 deficiency | Vitamin PP deficiency | Pellagra | Niacin deficiency | Nicotinamide deficiency | Nicotinic acid deficiency | Vitamin PP deficiency | Vitamin B3 deficiency | Pellagra (disorder) | Niacin deficiency | Niacin deficiency (disorder)
+BMGC_DS16439,BMG_DS062821,723363009,"Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome",,,,,,,C4317151,,137940,MONDO:0019073,hypotrichosis-lymphedema-telangiectasia-renal defect syndrome,"Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome (disorder) | Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome | Hypotrichosis, lymphoedema, telangiectasia, renal defect syndrome | HLTRS (hypotrichosis, lymphedema, telangiectasia, renal defect) syndrome | HLTRS (hypotrichosis, lymphoedema, telangiectasia, renal defect) syndrome"
+BMGC_DS16440,BMG_DS062823,,COLE-CARPENTER SYNDROME 1,,,,,,,C4317154,,176790;112240,MONDO:0007204,Cole-Carpenter syndrome 1,
+BMGC_DS16441,BMG_DS062824,,Adolescent Obesity,Pediatric Obesity,,,,,,C4317171,D063766,,,,
+BMGC_DS16442,BMG_DS062826,733601006,Congenital disorder of glycosylation type 1q,,,,,,,C4317224,,612379,MONDO:0012885,SRD5A3-congenital disorder of glycosylation,Congenital disorder of glycosylation type 1q (disorder) | SRD5A3-CDG - steroid 5 alpha-reductase 3 congenital disorder of glycosylation | Congenital disorder of glycosylation type 1q | Congenital disorder of glycosylation type Iq
+BMGC_DS16443,BMG_DS062827,733451007,Congenital disorder of glycosylation type 1s,,,,,,,C4317295,,300884,MONDO:0010472,"developmental and epileptic encephalopathy, 36",Congenital disorder of glycosylation type Is | ALG13-CDG (congenital disorder of glycosylation) | Congenital disorder of glycosylation type 1s | Congenital disorder of glycosylation type 1s (disorder)
+BMGC_DS16444,BMG_DS062829,4320005,Factor V deficiency,,,,,,,C4317320,,MTHU023372,MONDO:0020586,factor V deficiency,Factor V deficiency | Factor V deficiency (disorder)
+BMGC_DS16445,BMG_DS062830,,Juvenile Absence Epilepsy,"Epilepsy, Absence",,,,DOID:0070309,absence epilepsy,C4317339,D004832,,MONDO:0800453,juvenile absence epilepsy,
+BMGC_DS16446,BMG_DS062831,,,,,,,,,C4318479,,,MONDO:0015892,growth hormone insensitivity syndrome,
+BMGC_DS16447,BMG_DS062840,,BARDET-BIEDL SYNDROME 21,,,,,DOID:0081010,Bardet-Biedl syndrome 21,C4319932,,617406;614477,MONDO:0044308,bardet-biedl syndrome 21,
+BMGC_DS16448,BMG_DS062841,,,,,,,,,C4321245,,,MONDO:0004747,cleft lip,
+BMGC_DS16449,BMG_DS062857,783696009,Hyperandrogenism due to cortisone reductase deficiency,,,,,,,C4329210,,,,,Hyperandrogenism due to cortisone reductase deficiency | Hyperandrogenism due to cortisone reductase deficiency (disorder) | 11-beta-hydroxysteroid dehydrogenase deficiency type 1
+BMGC_DS16450,BMG_DS062860,,,,,,,DOID:0070629,acute myeloid leukemia with CBFA2T3-GLIS2 fusion,C4329266,,,,,
+BMGC_DS16451,BMG_DS062864,771445001,Autosomal recessive infantile hypercalcemia,,,,,,,C4329374,,,MONDO:0000212,"hypercalcemia, infantile",Autosomal recessive infantile hypercalcemia (disorder) | Autosomal recessive infantile hypercalcaemia | Familial infantile hypercalcaemia with suppressed intact parathyroid hormone | Autosomal recessive infantile hypercalcemia | Familial infantile hypercalcemia with suppressed intact parathyroid hormone
+BMGC_DS16452,BMG_DS062871,,,,,,,,,C4329780,,,MONDO:0100291,early T cell progenitor acute lymphoblastic leukemia,
+BMGC_DS16453,BMG_DS062883,,,,,,,,,C4331262,,,MONDO:0016736,rosette-forming glioneuronal tumor of fourth ventricule,
+BMGC_DS16454,BMG_DS062888,,,,,,,,,C4476553,,,MONDO:0020438,atrial septal aneurysm,
+BMGC_DS16455,BMG_DS062893,,"CILIARY DYSKINESIA, PRIMARY, 36, X-LINKED",,,,,DOID:0111850,primary ciliary dyskinesia 36,C4478372,,300933;300991,MONDO:0010517,"ciliary dyskinesia, primary, 36, X-linked",
+BMGC_DS16456,BMG_DS062894,,,,,,,,,C4478379,,300997,MONDO:0030907,"intellectual disability, X-linked 106",
+BMGC_DS16457,BMG_DS062895,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 35",,,,,DOID:0080241,syndromic X-linked mental retardation 35,C4478383,,300998;312173,MONDO:0030908,"intellectual disability, X-linked, syndromic, 35",
+BMGC_DS16458,BMG_DS062901,,NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1,,,,,DOID:0080692,Noonan syndrome-like disorder with loose anagen hair 1,C4478716,,607721;602775,MONDO:0054637,Noonan syndrome-like disorder with loose anagen hair 1,
+BMGC_DS16459,BMG_DS062903,,,,,,,,,C4478940,,613735,MONDO:0100478,brain malformations with or without urinary tract defects,
+BMGC_DS16460,BMG_DS062904,,"MYASTHENIC SYNDROME, CONGENITAL, 22",,,,,DOID:0080587,congenital myasthenic syndrome 22,C4479088,,616224;609557,MONDO:0044299,"myasthenic syndrome, congenital, 22",
+BMGC_DS16461,BMG_DS062906,,CONGENITAL MYOPATHY 24,,,,,DOID:0110933,nemaline myopathy 11,C4479186,,608517;617336,MONDO:0015023,MYPN-related myopathy,
+BMGC_DS16462,BMG_DS062907,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 51,,,,,DOID:0080433,developmental and epileptic encephalopathy 51,C4479208,,154100;617339,MONDO:0015025,"developmental and epileptic encephalopathy, 51",
+BMGC_DS16463,BMG_DS062908,,CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2,,,,,,,C4479220,,617341;613128,MONDO:0015026,cerebroretinal microangiopathy with calcifications and cysts 2,
+BMGC_DS16464,BMG_DS062909,,HYPERPARATHYROIDISM 4,,,,,,,C4479229,,617343;603716,MONDO:0024570,hyperparathyroidism 4,
+BMGC_DS16465,BMG_DS062910,,,,,,,,,C4479235,,617349,MONDO:0044301,"aortic aneurysm, familial thoracic 11, susceptibility to",
+BMGC_DS16466,BMG_DS062911,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 52,,,,,DOID:0080455,developmental and epileptic encephalopathy 52,C4479236,,617350;600235,MONDO:0033361,"developmental and epileptic encephalopathy, 52",
+BMGC_DS16467,BMG_DS062912,,"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER",,,,,DOID:0112247,"congenital heart defects, dysmorphic facial features, and intellectual developmental disorder",C4479246,,617360;603309,MONDO:0044302,"congenital heart defects, dysmorphic facial features, and intellectual developmental disorder",
+BMGC_DS16468,BMG_DS062913,,CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA,,,,,,,C4479250,,605435;617364,MONDO:0044303,congenital heart defects and ectodermal dysplasia,
+BMGC_DS16469,BMG_DS062914,,PEROXISOME BIOGENESIS DISORDER 10B,,,,,DOID:0081440,Peroxisome biogenesis disorder 10B,C4479254,,617370;603164,MONDO:0054549,peroxisome biogenesis disorder 10B,
+BMGC_DS16470,BMG_DS062915,,"AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 2",,,,,,,C4479260,,617383;605427,MONDO:0054551,"avascular necrosis of femoral head, primary, 2",
+BMGC_DS16471,BMG_DS062916,,"HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT",,,,,,,C4479270,,617384;606060,MONDO:0044304,hyperphenylalaninemia due to DNAJC12 deficiency,
+BMGC_DS16472,BMG_DS062917,,AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS,,,,,,,C4479278,,617388;606636,MONDO:0060457,autoinflammation with arthritis and dyskeratosis,
+BMGC_DS16473,BMG_DS062918,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 53,,,,,DOID:0080464,developmental and epileptic encephalopathy 53,C4479313,,604297;617389,MONDO:0033362,"developmental and epileptic encephalopathy, 53",
+BMGC_DS16474,BMG_DS062919,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 54,,,,,DOID:0080418,developmental and epileptic encephalopathy 54,C4479319,,602869;617391,MONDO:0033363,"developmental and epileptic encephalopathy, 54",
+BMGC_DS16475,BMG_DS062920,,"ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE",,,,,DOID:0111650,ectodermal dysplasia 13,C4479322,,609898;617392,MONDO:0044305,"ectodermal dysplasia 13, hair/tooth type",
+BMGC_DS16476,BMG_DS062921,,"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION",,,,,,,C4479333,,617393;610672,MONDO:0044306,"neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination",
+BMGC_DS16477,BMG_DS062922,,"SCLEROSING CHOLANGITIS, NEONATAL",,,,,,,C4479344,,605755;617394,MONDO:0018816,isolated neonatal sclerosing cholangitis,
+BMGC_DS16478,BMG_DS062923,1197753005,COG2-related congenital disorder of glycosylation,,,,,,,C4479353,,617395,MONDO:0054559,"congenital disorder of glycosylation, type IIq",COG2-related congenital disorder of glycosylation | COG2-CDG - component of oligomeric golgi complex 2 - congenital disorder of glycosylation | Component of oligomeric golgi complex 2-related congenital disorder of glycosylation (disorder) | Component of oligomeric golgi complex 2-related congenital disorder of glycosylation
+BMGC_DS16479,BMG_DS062924,,ANAUXETIC DYSPLASIA 2,,,,,DOID:0080962,anauxetic dysplasia 2,C4479357,,617396;602486,MONDO:0054561,anauxetic dysplasia 2,
+BMGC_DS16480,BMG_DS062925,,PSEUDO-TORCH SYNDROME 2,,,,,,,C4479376,,617397;607057,MONDO:0018828,pseudo-TORCH syndrome 2,
+BMGC_DS16481,BMG_DS062926,,"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC",,,,,,,C4479387,,108746;617402,MONDO:0027462,autosomal recessive cutis laxa type 2C,
+BMGC_DS16482,BMG_DS062927,,"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID",,,,,,,C4479409,,617403;607027,MONDO:0027451,autosomal recessive cutis laxa type 2D,
+BMGC_DS16483,BMG_DS062928,,"MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY",,,,,DOID:0080197,congenital muscular dystrophy with cataracts and intellectual disability,C4479410,,617404;607875,MONDO:0024607,congenital muscular dystrophy with cataracts and intellectual disability,
+BMGC_DS16484,BMG_DS062929,,SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY,,,,,,,C4479416,,617405,MONDO:0054565,short-rib thoracic dysplasia 17 with or without polydactyly,
+BMGC_DS16485,BMG_DS062930,,DIAMOND-BLACKFAN ANEMIA 16,,,,,DOID:0111893,Diamond-Blackfan anemia 16,C4479424,,607526;617408,MONDO:0044309,Diamond-Blackfan anemia 16,
+BMGC_DS16486,BMG_DS062931,,DIAMOND-BLACKFAN ANEMIA 17,,,,,DOID:0111880,Diamond-Blackfan anemia 17,C4479428,,617409;603702,MONDO:0044310,Diamond-Blackfan anemia 17,
+BMGC_DS16487,BMG_DS062932,,"BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY",,,,,DOID:0070415,"brachycephaly, trichomegaly, and developmental delay",C4479431,,617412;603683,MONDO:0044311,"brachycephaly, trichomegaly, and developmental delay",
+BMGC_DS16488,BMG_DS062933,,IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES,,,,,,,C4479452,,605744;617425,MONDO:0044312,immunoskeletal dysplasia with neurodevelopmental abnormalities,
+BMGC_DS16489,BMG_DS062935,,,,,,,,,C4479476,,617432,MONDO:0044313,"intellectual disability, autosomal recessive 60",
+BMGC_DS16490,BMG_DS062936,,RETINITIS PIGMENTOSA 78,,,,,,,C4479481,,616432;617433,MONDO:0044314,retinitis pigmentosa 78,
+BMGC_DS16491,BMG_DS062937,,LOPES-MACIEL-RODAN SYNDROME,,,,,,,C4479491,,613004;617435,MONDO:0054573,Lopes-Maciel-Rodan syndrome,
+BMGC_DS16492,BMG_DS062938,,CRANIOSYNOSTOSIS 7,,,,,DOID:0060912,craniosynostosis 7,C4479496,,617439,MONDO:0044315,craniosynostosis 7,
+BMGC_DS16493,BMG_DS062939,,"THROMBOCYTOPENIA, ANEMIA, AND MYELOFIBROSIS",,,,,,,C4479504,,617441;606520,MONDO:0044316,"thrombocytopenia, anemia, and myelofibrosis",
+BMGC_DS16494,BMG_DS062940,,PREMATURE OVARIAN FAILURE 13,,,,,DOID:0080870,primary ovarian insufficiency 13,C4479510,,617442;603382,MONDO:0044317,premature ovarian failure 13,
+BMGC_DS16495,BMG_DS062941,,"BLEEDING DISORDER, PLATELET-TYPE, 21",,,,,,,C4479515,,617443;193067,MONDO:0054577,"bleeding disorder, platelet-type, 21",
+BMGC_DS16496,BMG_DS062942,,JANSEN-DE VRIES SYNDROME,,,,,,,C4479517,,617450;605100,MONDO:0044318,intellectual developmental disorder with gastrointestinal difficulties and high pain threshold,
+BMGC_DS16497,BMG_DS062943,,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES",,,,,,,C4479520,,612021;617452,MONDO:0044319,"intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies",
+BMGC_DS16498,BMG_DS062944,,RETINITIS PIGMENTOSA 79,,,,,,,C4479526,,142600;617460,MONDO:0044320,retinitis pigmentosa 79,
+BMGC_DS16499,BMG_DS062945,,TOWNES-BROCKS SYNDROME 2,,,,,,,C4479534,,607861;617466,MONDO:0054582,Townes-Brocks syndrome 2,
+BMGC_DS16500,BMG_DS062946,,"ARTHROGRYPOSIS MULTIPLEX CONGENITA 1, NEUROGENIC, WITH MYELIN DEFECT",,,,,DOID:0080978,arthrogryposis multiplex congenita-1,C4479539,,608303;617468,MONDO:0060486,"arthrogryposis multiplex congenita 1, neurogenic, with myelin defect",
+BMGC_DS16501,BMG_DS062947,,SPECIFIC GRANULE DEFICIENCY 2,,,,,,,C4479548,,617475;601736,MONDO:0044208,specific granule deficiency 2,
+BMGC_DS16502,BMG_DS062948,,STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME,,,,,,,C4479549,,617478;617449,MONDO:0044321,structural heart defects and renal anomalies syndrome,
+BMGC_DS16503,BMG_DS062949,,,,,,,,,C4479552,,617480,MONDO:0060489,"46,XX sex reversal 4",
+BMGC_DS16504,BMG_DS062950,1222657001,PRUNE1-related neurological syndrome,,,,,,,C4479566,,617481,MONDO:0060490,"neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies",Prune exopolyphosphatase 1-related neurological syndrome (disorder) | PRUNE1-related neurological syndrome | Prune exopolyphosphatase 1-related neurological syndrome
+BMGC_DS16505,BMG_DS062951,,NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS,,,,,DOID:0112276,neurodevelopmental disorder with involuntary movements,C4479569,,617493;139311,MONDO:0060491,neurodevelopmental disorder with involuntary movements,
+BMGC_DS16506,BMG_DS062952,,NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2,,,,,DOID:0080693,Noonan syndrome-like disorder with loose anagen hair 2,C4479577,,617506;600590,MONDO:0054588,Noonan syndrome-like disorder with loose anagen hair 2,
+BMGC_DS16507,BMG_DS062953,,IMMUNODEFICIENCY 52,,,,,DOID:0111983,immunodeficiency 52,C4479588,,617514;602354,MONDO:0044721,severe combined immunodeficiency due to LAT deficiency,
+BMGC_DS16508,BMG_DS062955,,STANKIEWICZ-ISIDOR SYNDROME,,,,,,,C4479599,,617516;604450,MONDO:0054591,Stankiewicz-Isidor syndrome,
+BMGC_DS16509,BMG_DS062956,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS",,,,,,,C4479603,,606214;617519,MONDO:0060496,"neurodevelopmental disorder with hypotonia, neuropathy, and deafness",
+BMGC_DS16510,BMG_DS062957,,"MICROCEPHALY 18, PRIMARY, AUTOSOMAL DOMINANT",,,,,DOID:0070295,primary autosomal dominant microcephaly 18,C4479608,,617485;617520,MONDO:0054593,"microcephaly 18, primary, autosomal dominant",
+BMGC_DS16511,BMG_DS062958,,NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS,,,,,DOID:0080312,neurodevelopmental disorder with midbrain and hindbrain malformations,C4479613,,607560;617523,MONDO:0056797,neurodevelopmental disorder with midbrain and hindbrain malformations,
+BMGC_DS16512,BMG_DS062959,,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 2,,,,,DOID:0080248,erythrokeratodermia variabilis et progressiva 2,C4479618,,605425;617524,MONDO:0033012,erythrokeratodermia variabilis et progressiva 2,
+BMGC_DS16513,BMG_DS062960,,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 3,,,,,DOID:0080249,erythrokeratodermia variabilis et progressiva 3,C4479619,,121014;617525,MONDO:0033013,erythrokeratodermia variabilis et progressiva 3,
+BMGC_DS16514,BMG_DS062961,,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 4,,,,,DOID:0080250,erythrokeratodermia variabilis et progressiva 4,C4479620,,617526;136440,MONDO:0033014,erythrokeratodermia variabilis et progressiva 4,
+BMGC_DS16515,BMG_DS062962,1217367007,PLAA-associated neurodevelopmental disorder,,,,,,,C4479631,,617527,MONDO:0060502,"neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies",Phospholipase A2 activating protein-associated neurodevelopmental disorder (disorder) | Phospholipase A2 activating protein-associated neurodevelopmental disorder | PLAA-associated neurodevelopmental disorder | PLAAND - phospholipase A2 activating protein-associated neurodevelopmental disorder
+BMGC_DS16516,BMG_DS062963,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES,,,,,,,C4479636,,617532;605763,MONDO:0044322,intellectual developmental disorder with neuropsychiatric features,
+BMGC_DS16517,BMG_DS062964,1304277005,"Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1-4 mutation",,,,,,,C4479637,,617537,MONDO:0044323,Rahman syndrome,"Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1.4 linker histone, cluster member mutation (disorder) | Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1-4 mutation | H1-4-related neurodevelopmental disorder | Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1.4 linker histone, cluster member mutation | Rahman syndrome"
+BMGC_DS16518,BMG_DS062965,,"GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS 2, WITH IMPAIRED INTELLECTUAL DEVELOPMENT",,,,,,,C4479640,,617542;120470,MONDO:0054602,"gaze palsy, familial horizontal, with progressive scoliosis, 2",
+BMGC_DS16519,BMG_DS062967,,RETINAL DYSTROPHY WITH OR WITHOUT MACULAR STAPHYLOMA,,,,,,,C4479651,,617547,MONDO:0060507,retinal dystrophy with or without macular staphyloma,
+BMGC_DS16520,BMG_DS062968,1186730002,Gabriele-de Vries syndrome,,,,,,,C4479652,,617557,MONDO:0044738,Gabriele de Vries syndrome,YY1 haploinsufficiency syndrome | Gabriele-de Vries syndrome | Gabriele-de Vries syndrome (disorder)
+BMGC_DS16521,BMG_DS062969,1217379007,NKX6-2-related autosomal recessive hypomyelinating leukodystrophy,,,,,,,C4479653,,617560,MONDO:0033043,"spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy","NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (disorder) | NK6 homeobox 2-related autosomal recessive hypomyelinating leucodystrophy | NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy | NKX6-2-related autosomal recessive hypomyelinating leucodystrophy | NKX6-2-related autosomal recessive hypomyelinating leukodystrophy | Autosomal recessive hypomyelinating leukodystrophy, progressive spastic ataxia | SPAX8 - spastic ataxia 8 | Autosomal recessive hypomyelinating leucodystrophy, progressive spastic ataxia"
+BMGC_DS16522,BMG_DS062970,,COHEN-GIBSON SYNDROME,,,,,,,C4479654,,617561;605984,MONDO:0060510,Cohen-Gibson syndrome,
+BMGC_DS16523,BMG_DS062971,,MEIER-GORLIN SYNDROME 8,,,,,DOID:0080255,Meier-Gorlin syndrome 8,C4479655,,602696;617564,MONDO:0033046,Meier-Gorlin syndrome 8,
+BMGC_DS16524,BMG_DS062972,,PERRAULT SYNDROME 6,,,,,DOID:0080256,Perrault syndrome 6,C4479656,,607435;617565,MONDO:0033047,Perrault syndrome 6,
+BMGC_DS16525,BMG_DS062975,,"HYPERLIPOPROTEINEMIA, TYPE III, DUE TO APOE2",,,,,,,C4479659,,107741,,,
+BMGC_DS16526,BMG_DS062976,,"ADRENAL INSUFFICIENCY, NR5A1-RELATED",,,,,DOID:0080864,primary ovarian insufficiency 7,C4479664,,612964;184757,,,
+BMGC_DS16527,BMG_DS063000,,Epileptic Syndromes,Epileptic Syndromes,,,,,,C4505072,D000073376,,MONDO:0015650,epilepsy syndrome,
+BMGC_DS16528,BMG_DS063011,,Xp21 Contiguous Gene Deletion Syndrome,"Hypoadrenocorticism, Familial",,,,,,C4505291,D000075262,300679,MONDO:0010399,chromosome Xp21 deletion syndrome,
+BMGC_DS16529,BMG_DS063016,,Diverticular Bleeding,Diverticular Diseases,,,,,,C4505353,D000076385,,,,
+BMGC_DS16530,BMG_DS063019,,Mycoplasma ovipneumoniae Infection,"Pneumonia, Mycoplasma",,,,DOID:13276,Mycoplasma pneumoniae pneumonia,C4505422,D011019,,,,
+BMGC_DS16531,BMG_DS063020,,Mycoplasma dispar Infection,"Pneumonia, Mycoplasma",,,,DOID:13276,Mycoplasma pneumoniae pneumonia,C4505423,D011019,,,,
+BMGC_DS16532,BMG_DS063025,,Generalized Absence Seizures,Seizures,,,,,,C4505436,D012640,,,,
+BMGC_DS16533,BMG_DS063026,,Trichophyton mentagrophytes Infection,Tinea,,,,,,C4505442,D014005,,,,
+BMGC_DS16534,BMG_DS063027,,HIV Coinfection,HIV Infections,,,,,,C4505456,D015658,,,,
+BMGC_DS16535,BMG_DS063036,,"Chemical and Drug Induced Liver Injury, Chronic","Chemical and Drug Induced Liver Injury, Chronic",,,,,,C4505492,D056487,,,,
+BMGC_DS16536,BMG_DS063037,,"Chemical-Induced Liver Injury, Chronic","Chemical and Drug Induced Liver Injury, Chronic",,,,,,C4505493,D056487,,,,
+BMGC_DS16537,BMG_DS063041,,,,,,,,,C4509020,,,MONDO:0015558,isolated bone marrow mastocytosis,
+BMGC_DS16538,BMG_DS063044,,Senile systemic amyloidosis (SSA),,,,E85.82,DOID:0050638,transthyretin amyloidosis,C4509024,,,,,
+BMGC_DS16539,BMG_DS063137,,Celiac gluten-sensitive enteropathy,,DA95,Coeliac disease,K90.0,,,C4509268,,,,,
+BMGC_DS16540,BMG_DS063276,,,,,,,,,C4509816,,,MONDO:0056806,non-small cell squamous lung carcinoma,
+BMGC_DS16541,BMG_DS063279,723309006,Endocrine-cerebro-osteodysplasia syndrome,,,,,,,C4509819,,,,,Endocrine-cerebro-osteodysplasia syndrome (disorder) | Endocrine-cerebro-osteodysplasia syndrome | ECO syndrome | ECO (endocrine-cerebro-osteodysplasia) syndrome | Endocrine cerebroosteodysplasia syndrome
+BMGC_DS16542,BMG_DS063280,723334006,FADD-related immunodeficiency,,,,,,,C4509831,,,,,FADD-related immunodeficiency | Immunodeficiency due to mutation of FAS-associated protein with death domain gene (disorder) | Immunodeficiency due to mutation of FAS-associated protein with death domain gene | FADD (FAS-associated protein with death domain) related immunodeficiency
+BMGC_DS16543,BMG_DS063281,723359002,Familial acute necrotizing encephalopathy,,,,,,,C4509836,,,,,Familial acute necrotizing encephalopathy (disorder) | Familial acute necrotizing encephalopathy | Familial acute necrotising encephalopathy | Recurrent acute necrotizing encephalopathy | Recurrent acute necrotising encephalopathy
+BMGC_DS16544,BMG_DS063285,723384004,Mendelian susceptibility to mycobacterial disease due to complete ISG15 deficiency,,,,,,,C4509853,,,,,Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency | Mendelian susceptibility to mycobacterial disease due to complete ISG15 deficiency | Mendelian susceptibility to mycobacterial disease due to complete ISG15 (interferon stimulated gene 15) deficiency
+BMGC_DS16545,BMG_DS063286,723385003,Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency,,,,,,,C4509854,,,,,Mendelian susceptibility to mycobacterial disease due to partial interferon regulatory factor 8 deficiency (disorder) | Mendelian susceptibility to mycobacterial disease due to partial interferon regulatory factor 8 deficiency | Mendelian susceptibility to mycobacterial disease due to partial IRF8 (interferon regulatory factor 8) deficiency | Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency
+BMGC_DS16546,BMG_DS063287,723386002,Mendelian susceptibility to mycobacterial disease due to partial STAT1 deficiency,,,,,,,C4509855,,,,,Mendelian susceptibility to mycobacterial disease due to partial signal transducer and activator of transcription 1 deficiency (disorder) | Mendelian susceptibility to mycobacterial disease due to partial signal transducer and activator of transcription 1 deficiency | Mendelian susceptibility to mycobacterial disease due to partial STAT1 deficiency | Mendelian susceptibility to mycobacterial disease due to partial STAT1 (signal transducer and activator of transcription 1) deficiency
+BMGC_DS16547,BMG_DS063292,723404002,Microcephalic osteodysplastic dysplasia Saul Wilson type,,,,,,,C4509877,,,,,Microcephalic osteodysplastic dysplasia Saul Wilson type (disorder) | Microcephalic osteodysplastic dysplasia Saul Wilson type
+BMGC_DS16548,BMG_DS063295,723407009,Muscular dystrophy Selcen type,,,,,,,C4509880,,,,,Muscular dystrophy Selcen type (disorder) | Muscular dystrophy Selcen type | Selcen muscular dystrophy
+BMGC_DS16549,BMG_DS063296,723408004,Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus,,,,,,,C4509881,,,MONDO:0020382,multifocal pattern dystrophy simulating fundus flavimaculatus,Multifocal pattern dystrophy simulating Stargardt disease | Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus (disorder) | Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus | Multifocal pattern dystrophy simulating fundus flavimaculatus
+BMGC_DS16550,BMG_DS063308,723441001,Non-progressive cerebellar ataxia with intellectual disability,,,,,,,C4509917,,,,,Non-progressive cerebellar ataxia with intellectual disability (disorder) | Non-progressive cerebellar ataxia with intellectual disability
+BMGC_DS16551,BMG_DS063309,723448007,Polyvalvular heart disease syndrome,,,,,,,C4509918,,,MONDO:0016460,polyvalvular heart disease syndrome,Polyvalvular heart disease syndrome (disorder) | Polyvalvular heart disease syndrome
+BMGC_DS16552,BMG_DS063311,723452007,"Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome",,,,,,,C4509920,,,,,"Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) | Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome | PHARC (polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract) syndrome | PHARC syndrome | Peripheral neuropathy Fiskerstrand type"
+BMGC_DS16553,BMG_DS063315,,,,,,,,,C4509932,,,MONDO:0016996,NK-cell enteropathy,
+BMGC_DS16554,BMG_DS063316,723497003,Peripheral neuropathy with sensorineural hearing impairment syndrome,,,,,,,C4509933,,,MONDO:0015351,neuropathy with hearing impairment,Peripheral neuropathy with sensorineural hearing impairment syndrome (disorder) | Peripheral neuropathy with sensorineural hearing impairment syndrome | Neuropathy with hearing impairment
+BMGC_DS16555,BMG_DS063321,723578001,Terminal osseous dysplasia and pigmentary defect syndrome,,,,,,,C4509953,,,,,Terminal osseous dysplasia and pigmentary defect syndrome (disorder) | Terminal osseous dysplasia and pigmentary defect syndrome
+BMGC_DS16556,BMG_DS063335,723716009,Severe generalized recessive dystrophic epidermolysis bullosa,,,,,,,C4510043,,,,,Severe generalized recessive dystrophic epidermolysis bullosa (disorder) | Severe generalized recessive dystrophic epidermolysis bullosa | Severe generalised recessive dystrophic epidermolysis bullosa | Autosomal recessive dystrophic epidermolysis bullosa generalisata gravis | Autosomal recessive dystrophic epidermolysis bullosa Hallopeau Siemens type
+BMGC_DS16557,BMG_DS063358,723866006,Idiopathic ventricular fibrillation not Brugada type,,,,,,,C4510132,,,,,Idiopathic ventricular fibrillation not Brugada type (disorder) | Idiopathic ventricular fibrillation not Brugada type
+BMGC_DS16558,BMG_DS063368,723993005,Sensorineural deafness with dilated cardiomyopathy syndrome,,,,,,,C4510220,,,,,Sensorineural deafness with dilated cardiomyopathy syndrome (disorder) | Sensorineural deafness with dilated cardiomyopathy syndrome
+BMGC_DS16559,BMG_DS063389,724094005,"Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome",,,,,,,C4510367,,,,,"Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome (disorder) | Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome"
+BMGC_DS16560,BMG_DS063390,724095006,Myopathy due to calsequestrin and SERCA1 protein overload,,,,,,,C4510368,,,,,Myopathy due to calsequestrin and sarcoplasmic/endoplasmic reticulum calcium ATPase 1 protein overload (disorder) | Myopathy due to calsequestrin and SERCA1 protein overload | Myopathy due to calsequestrin and sarcoplasmic/endoplasmic reticulum calcium ATPase 1 protein overload | Myopathy due to calsequestrin and SERCA1 (sarcoplasmic/endoplasmic reticulum calcium ATPase 1) protein overload
+BMGC_DS16561,BMG_DS063393,724141003,Microcephalic primordial dwarfism due to ZNF335 deficiency,,,,,,,C4510378,,,,,Microcephalic primordial dwarfism due to zinc finger protein 335 deficiency (disorder) | Microcephalic primordial dwarfism due to ZNF335 deficiency | Microcephalic primordial dwarfism due to zinc finger protein 335 deficiency | Microcephalic primordial dwarfism due to ZNF335 (zinc finger protein 335) deficiency | Microcephalic primordial dwarfism Walsh type
+BMGC_DS16562,BMG_DS063395,724145007,"Metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome",,,,,,,C4510380,,,,,"Metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome (disorder) | Metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome"
+BMGC_DS16563,BMG_DS063396,724172004,McLeod neuroacanthocytosis syndrome,,,,,,,C4510408,,,,,McLeod neuroacanthocytosis syndrome (disorder) | McLeod neuroacanthocytosis syndrome | X-linked McLeod syndrome
+BMGC_DS16564,BMG_DS063398,724179008,Laron syndrome with immunodeficiency,,,,,,,C4510411,,,,,Laron syndrome with immunodeficiency (disorder) | Laron syndrome with immunodeficiency | Laron-like syndrome | Short stature due to STAT5b (signal transducer and activator of transcription 5b) deficiency
+BMGC_DS16565,BMG_DS063422,724277002,Congenital ichthyosis with hypotrichosis syndrome,,,,,,,C4510566,,,,,"Congenital ichthyosis with hypotrichosis syndrome (disorder) | Congenital ichthyosis with hypotrichosis syndrome | Ichthyosis, follicular atrophoderma, hypotrichosis syndrome"
+BMGC_DS16566,BMG_DS063423,724281002,"Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome",,,,,,,C4510568,,,MONDO:0016393,hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome,"Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome (disorder) | Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome | Bosma Henkin Christiansen syndrome"
+BMGC_DS16567,BMG_DS063428,724344004,Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency,,,,,,,C4510605,,,,,Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (disorder) | Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
+BMGC_DS16568,BMG_DS063429,724349009,"Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome",,,,,,,C4510610,,,MONDO:0019195,hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome,"Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Hereditary inclusion body myopathy type 3 | Inclusion body myopathy type 3"
+BMGC_DS16569,BMG_DS063432,724356003,Hereditary combined deficiency of vitamin K-dependent clotting factors,,,,,DOID:0112172,hereditary combined deficiency of vitamin K-dependent clotting factors,C4510617,,,MONDO:0015722,congenital vitamin K-dependent coagulation factors deficiency,"Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder) | Hereditary combined deficiency of vitamin K-dependent clotting factors | Hereditary combined deficiency of factors II, VII, IX and X"
+BMGC_DS16570,BMG_DS063433,724361001,Hepatic veno-occlusive disease with immunodeficiency syndrome,,,,,,,C4510630,,,,,"Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | Hepatic veno-occlusive disease with immunodeficiency syndrome | VODI (veno-occlusive disease, immunodeficiency) syndrome | VODI syndrome"
+BMGC_DS16571,BMG_DS063442,724498004,Pneumonia caused by Chlamydia pneumoniae,,,,,,,C4510691,,,,,Pneumonia caused by Chlamydia pneumoniae (disorder) | Pneumonia caused by Chlamydia pneumoniae
+BMGC_DS16572,BMG_DS063456,725029001,Frontonasal dysplasia with alopecia and genital anomaly syndrome,,,,,,,C4510728,,,,,Frontonasal dysplasia with alopecia and genital anomaly syndrome (disorder) | Frontonasal dysplasia with alopecia and genital anomaly syndrome | Craniofrontonasal dysplasia with alopecia and hypogonadism | Frontonasal dysplasia with alopecia and genital abnomality | ALX4 (human aristaless-like 4) related frontonasal dysplasia with alopecia and genital anomaly
+BMGC_DS16573,BMG_DS063461,725045004,"46,XY partial gonadal dysgenesis",,,,,,,C4510744,,,MONDO:0016674,"46,XY partial gonadal dysgenesis","46,XY partial gonadal dysgenesis (disorder) | 46,XY partial gonadal dysgenesis"
+BMGC_DS16574,BMG_DS063463,725027004,Muscle and heart glycogen synthase deficiency,,,,,,,C4510752,,,,,Muscle and heart glycogen synthase deficiency (disorder) | Muscle and heart glycogen synthase deficiency | Glycogen storage disease due to muscle and heart glycogen synthase deficiency | Glycogen storage disease type 0b | Glycogenosis due to muscle and heart glycogen synthase deficiency | Glycogenosis type 0b
+BMGC_DS16575,BMG_DS063464,725026008,Hepatic glycogen synthase deficiency,,,,,,,C4510753,,,,,Hepatic glycogen synthase deficiency (disorder) | Hepatic glycogen synthase deficiency | Glycogen storage disease due to hepatic glycogen synthase deficiency | Glycogen storage disease due to liver glycogen synthase deficiency | Glycogen storage disease type 0a | Glycogenosis type 0a
+BMGC_DS16576,BMG_DS063467,724226009,Infantile osteopetrosis with neuroaxonal dysplasia syndrome,,,,,,,C4510764,,,,,Infantile osteopetrosis with neuroaxonal dysplasia syndrome (disorder) | Infantile osteopetrosis with neuroaxonal dysplasia syndrome | Infantile osteopetrosis with neuroaxonal dysplasia
+BMGC_DS16577,BMG_DS063484,725099009,Craniometadiaphyseal dysplasia wormian bone type,,,,,,,C4510809,,269300,MONDO:0010014,"craniometadiaphyseal dysplasia, wormian bone type",Craniometadiaphyseal dysplasia wormian bone type (disorder) | Craniometadiaphyseal dysplasia wormian bone type
+BMGC_DS16578,BMG_DS063486,725105006,Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency,,,,,,,C4510815,,,,,Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I (disorder) | Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency | Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I
+BMGC_DS16579,BMG_DS063516,725135004,Combined immunodeficiency due to CD3gamma deficiency,,,,,,,C4510864,,,,,Combined immunodeficiency due to CD3gamma deficiency (disorder) | Combined immunodeficiency due to CD3gamma deficiency | Combined immunodeficiency due to CD3-gamma deficiency
+BMGC_DS16580,BMG_DS063518,725145002,"Atrial septal defect, atrioventricular conduction defect syndrome",,,,,,,C4510872,,,,,"Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Atrial septal defect, atrioventricular conduction defect syndrome"
+BMGC_DS16581,BMG_DS063519,725146001,Atypical juvenile parkinsonism,,,,,,,C4510873,,,MONDO:0018321,atypical juvenile parkinsonism,Atypical juvenile parkinsonism (disorder) | Atypical juvenile parkinsonism
+BMGC_DS16582,BMG_DS063521,725151007,Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency,,,,,,,C4510875,,,MONDO:0017903,autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency,Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency (disorder) | Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency | Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial IFNgammaR2 deficiency
+BMGC_DS16583,BMG_DS063523,725164008,Omodysplasia,,,,,DOID:0060288,omodysplasia,C4510897,,,MONDO:0017136,omodysplasia,Omodysplasia (disorder) | Omodysplasia
+BMGC_DS16584,BMG_DS063527,725286002,3-hydroxy-3-methylglutaryl-coenzyme A synthase deficiency,,,,,,,C4510940,,,,,Deficiency of 3-hydroxy-3-methylglutaryl-coenzyme A synthase (disorder) | 3-hydroxy-3-methylglutaryl-coenzyme A synthase deficiency | 3-hydroxy-3-methylglutaryl-CoA synthase deficiency | Deficiency of 3-hydroxy-3-methylglutaryl-coenzyme A synthase | HMG-coenzyme A synthase deficiency
+BMGC_DS16585,BMG_DS063529,725290000,Combined immunodeficiency due to partial RAG1 deficiency,,,,,,,C4510944,,,,,Combined immunodeficiency due to partial recombination-activating gene 1 deficiency (disorder) | Combined immunodeficiency due to partial RAG1 deficiency | Combined immunodeficiency due to partial recombination-activating gene 1 deficiency | Combined immunodeficiency with expansion of gamma delta T cell
+BMGC_DS16586,BMG_DS063530,725291001,Defect of purinergic receptor p2y G protein-coupled 12,,,,,,,C4510945,,,,,Defect of purinergic receptor p2y G protein-coupled 12 (disorder) | Defect of purinergic receptor p2y G protein-coupled 12 | ADP platelet receptor P2Y12 defect | P2Y12 (purinergic receptor p2y G protein-coupled 12) defect | P2Y12 defect
+BMGC_DS16587,BMG_DS063532,725163002,"X-linked spasticity, intellectual disability, epilepsy syndrome",,,,,,,C4510949,,,MONDO:0017856,X-linked spasticity-intellectual disability-epilepsy syndrome,"X-linked spasticity, intellectual disability, epilepsy syndrome (disorder) | X-linked spasticity, intellectual disability, epilepsy syndrome"
+BMGC_DS16588,BMG_DS063540,724555000,Puberty disorder due to estrogen resistance,,,,,,,C4510972,,,,,Puberty disorder due to estrogen resistance (disorder) | Puberty disorder due to estrogen resistance | Puberty disorder due to oestrogen resistance | Estrogen resistance syndrome | Oestrogen resistance syndrome
+BMGC_DS16589,BMG_DS063553,,,,,,,DOID:0070630,acute myeloid leukemia with KAT6A-CREBBP fusion,C4511003,,,MONDO:0018256,acute myeloid leukemia with t(8;16)(p11;p13) translocation,
+BMGC_DS16590,BMG_DS063554,725392005,Autosomal dominant striatal neurodegeneration,,,,,,,C4511004,,,,,Autosomal dominant striatal neurodegeneration (disorder) | Autosomal dominant striatal neurodegeneration | ADSD - autosomal dominant striatal neurodegeneration
+BMGC_DS16591,BMG_DS063566,725407006,Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type,,,,,,,C4511044,,,MONDO:0019522,recessive dystrophic epidermolysis bullosa-generalized other,Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type (disorder) | Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type | RDEB-O - recessive dystrophic epidermolysis bullosa-generalized other | RDEB-O - recessive dystrophic epidermolysis bullosa-generalised other
+BMGC_DS16592,BMG_DS063576,725420009,Congenital muscular dystrophy Paradas type,,,,,,,C4511057,,,MONDO:0016049,"congenital myopathy, Paradas type",Congenital muscular dystrophy Paradas type (disorder) | Congenital muscular dystrophy Paradas type | Congenital myopathy Paradas type
+BMGC_DS16593,BMG_DS063577,725431001,Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency,,,,,,,C4511091,,,MONDO:0017901,autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency,Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (disorder) | Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency | Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial IFNgammaR1 deficiency
+BMGC_DS16594,BMG_DS063578,725150008,Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency,,,,,,,C4511097,,,,,Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (disorder) | Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency | Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial IFNgammaR1 deficiency
+BMGC_DS16595,BMG_DS063579,725432008,Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency,,,,,,,C4511098,,,MONDO:0017902,autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency,Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency (disorder) | Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency | Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial IFNgammaR2 deficiency
+BMGC_DS16596,BMG_DS063580,725463007,Severe congenital hypochromic anemia with ringed sideroblasts,,,,,,,C4511137,,,,,Severe congenital hypochromic anemia with ringed sideroblasts (disorder) | Severe congenital hypochromic anemia with ringed sideroblasts | Severe congenital hypochromic anaemia with ringed sideroblasts | Severe congenital hypochromic sideroblastic anemia | Severe congenital hypochromic sideroblastic anaemia
+BMGC_DS16597,BMG_DS063581,725464001,Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy,,,,,,,C4511138,,,MONDO:0018002,adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy,Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy (disorder) | Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy | Adult-onset CPEO (chronic progressive external ophthalmoplegia) with mitochondrial myopathy
+BMGC_DS16598,BMG_DS063586,725588002,Bathing suit ichthyosis,,,,,,,C4511230,,,MONDO:0015085,bathing suit ichthyosis,Bathing suit ichthyosis (disorder) | Bathing suit ichthyosis
+BMGC_DS16599,BMG_DS063593,725590001,Butterfly-shaped pigmentary macular dystrophy,,,,,,,C4511237,,,MONDO:0100466,butterfly-shaped pigment dystrophy,Butterfly-shaped pigmentary macular dystrophy (disorder) | Butterfly-shaped pigmentary macular dystrophy | Butterfly-shaped pattern dystrophy | Butterfly-shaped pigment dystrophy
+BMGC_DS16600,BMG_DS063595,725592009,Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization,,,,,,,C4511239,,,MONDO:0019068,congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization,Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization (disorder) | Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization | Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunisation
+BMGC_DS16601,BMG_DS063647,725907002,Autosomal recessive limb girdle muscular dystrophy type 2Y,,,,,,,C4511482,,617072,MONDO:0014900,autosomal recessive limb-girdle muscular dystrophy type 2Y,"Autosomal recessive limb girdle muscular dystrophy type 2Y (disorder) | Autosomal recessive limb girdle muscular dystrophy type 2Y | Autosomal recessive muscular dystrophy due to LAP1B (lamin-associated protein 1B) deficiency | Autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency | Muscular dystrophy with progressive weakness, distal contracture and rigid spine"
+BMGC_DS16602,BMG_DS063654,725033008,Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement,,,,,,,C4511528,,,,,Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder) | Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement | Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis without severe ocular involvement | Renal hypomagnesemia type 3 | Renal hypomagnesaemia type 3
+BMGC_DS16603,BMG_DS063662,11047881000119101,Cannabis hyperemesis syndrome co-occurrent and due to cannabis abuse,,,,,,,C4511590,,,,,Cannabis hyperemesis syndrome co-occurrent and due to cannabis abuse (disorder) | Cannabis hyperemesis syndrome co-occurrent and due to cannabis abuse
+BMGC_DS16604,BMG_DS063663,11048011000119103,Cannabis hyperemesis syndrome co-occurrent and due to cannabis dependence,,,,,,,C4511594,,,,,Cannabis hyperemesis syndrome co-occurrent and due to cannabis dependence (disorder) | Cannabis hyperemesis syndrome co-occurrent and due to cannabis dependence
+BMGC_DS16605,BMG_DS063668,726018006,Autosomal dominant tubulointerstitial kidney disease,,,,,,,C4511620,,,MONDO:0008264,autosomal dominant medullary cystic kidney disease with or without hyperuricemia,Autosomal dominant medullary cystic kidney disease | Autosomal dominant tubulointerstitial kidney disease | Autosomal dominant tubulointerstitial kidney disease (disorder)
+BMGC_DS16606,BMG_DS063672,726031001,CAMOS syndrome,,,,,,,C4511633,,606937,MONDO:0019374,CAMOS syndrome,"Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | CAMOS syndrome | CAMOS (cerebellar ataxia, mental retardation, optic atrophy, skin abnormalities) syndrome | Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome | SCAR5 - spinocerebellar ataxia autosomal recessive 5"
+BMGC_DS16607,BMG_DS063675,726079008,Hereditary hypercarotenemia and vitamin A deficiency,,,,,,,C4511672,,,,,Hereditary hypercarotenemia and vitamin A deficiency (disorder) | Hereditary hypercarotenemia and vitamin A deficiency | Hereditary hypercarotenaemia and vitamin A deficiency
+BMGC_DS16608,BMG_DS063677,726106004,X-linked diffuse leiomyomatosis with Alport syndrome,,,,,,,C4511693,,,,,"X-linked diffuse leiomyomatosis with Alport syndrome (disorder) | X-linked diffuse leiomyomatosis with Alport syndrome | X-linked diffuse leiomyomatosis, Alport syndrome"
+BMGC_DS16609,BMG_DS063717,726614009,Autosomal recessive limb girdle muscular dystrophy type 2P,,,,,,,C4511963,,613818,MONDO:0013440,autosomal recessive limb-girdle muscular dystrophy type 2P,Autosomal recessive limb girdle muscular dystrophy type 2P (disorder) | Autosomal recessive limb girdle muscular dystrophy type 2P
+BMGC_DS16610,BMG_DS063719,726622002,Spastic paraplegia with Paget disease of bone syndrome,,,,,,,C4511969,,,MONDO:0018005,spastic paraplegia-Paget disease of bone syndrome,Spastic paraplegia with Paget disease of bone syndrome (disorder) | Spastic paraplegia with Paget disease of bone syndrome
+BMGC_DS16611,BMG_DS063723,726669007,"Central nervous system calcification, deafness, tubular acidosis, anemia syndrome",,,,,,,C4512024,,,MONDO:0017924,central nervous system calcification-deafness-tubular acidosis-anemia syndrome,"Central nervous system calcification, deafness, tubular acidosis, anemia syndrome (disorder) | Central nervous system calcification, deafness, tubular acidosis, anemia syndrome | Central nervous system calcification, deafness, tubular acidosis, anaemia syndrome | Yoshimura Takeshita syndrome"
+BMGC_DS16612,BMG_DS063728,726702005,Epileptic encephalopathy with global cerebral demyelination,,,,,,,C4512050,,,,,Epileptic encephalopathy with global cerebral demyelination (disorder) | Epileptic encephalopathy with global cerebral demyelination | Mitochondrial aspartate-glutamate carrier 1 deficiency
+BMGC_DS16613,BMG_DS063733,726732002,X-linked intellectual disability Nascimento type,,,,,,,C4512071,,,,,"X-linked intellectual disability Nascimento type (disorder) | X-linked intellectual disability Nascimento type | X-linked intellectual disability, nail dystrophy, seizures syndrome"
+BMGC_DS16614,BMG_DS063740,732246009,"X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency",,,,,,,C4517296,,,MONDO:0018495,X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome,"X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome | X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency (disorder) | X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency"
+BMGC_DS16615,BMG_DS063747,732264002,Coenzyme A synthase protein associated neurodegeneration,,,,,,,C4517377,,615643,MONDO:0014290,neurodegeneration with brain iron accumulation 6,Coenzyme A synthase protein associated neurodegeneration (disorder) | Coenzyme A synthase protein associated neurodegeneration | COASY protein-associated neurodegeneration | CoPAN - coenzyme A synthase protein associated neurodegeneration | Neurodegeneration with brain iron accumulation due to COASY mutation
+BMGC_DS16616,BMG_DS063751,732929002,Autosomal recessive limb girdle muscular dystrophy type 2S,,,,,,,C4517996,,615356,MONDO:0014144,autosomal recessive limb-girdle muscular dystrophy type R18,Autosomal recessive limb girdle muscular dystrophy type 2S (disorder) | Autosomal recessive limb girdle muscular dystrophy type 2S
+BMGC_DS16617,BMG_DS063752,732930007,Autosomal recessive limb girdle muscular dystrophy type 2T,,,,,,,C4518000,,615352,MONDO:0014142,autosomal recessive limb-girdle muscular dystrophy type 2T,Autosomal recessive limb girdle muscular dystrophy type 2T (disorder) | Autosomal recessive limb girdle muscular dystrophy type 2T
+BMGC_DS16618,BMG_DS063759,733623005,"Autism spectrum disorder, epilepsy, arthrogryposis syndrome",,,,,,,C4518080,,,,,"Autism spectrum disorder, epilepsy, arthrogryposis syndrome (disorder) | Autism spectrum disorder, epilepsy, arthrogryposis syndrome | SLC35A3-CDG - solute carrier family 35 member A3 congenital disorder of glycosylation"
+BMGC_DS16619,BMG_DS063766,733638006,Acral dystrophic epidermolysis bullosa,,,,,,,C4518087,,,MONDO:0015552,acral dystrophic epidermolysis bullosa,Acral dystrophic epidermolysis bullosa (disorder) | Acral dystrophic epidermolysis bullosa | Acral DEB (dystrophic epidermolysis bullosa)
+BMGC_DS16620,BMG_DS063814,724275005,Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency,,,,,,,C4518328,,,,,Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency (disorder) | Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency | Primary immunodeficiency due to MCM4 (mini-chromosome maintenance complex component 4) deficiency | Primary immunodeficiency due to MCM4 deficiency
+BMGC_DS16621,BMG_DS063815,724097003,"Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome",,,,,,,C4518329,,,,,"Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome (disorder) | Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome | Moyamoya disease, short stature, facial dysmorphism, hypergonadotropic hypogonadism"
+BMGC_DS16622,BMG_DS063817,,,,,,,,,C4518333,,,MONDO:0018448,clear cell papillary renal cell carcinoma,
+BMGC_DS16623,BMG_DS063820,734020000,Spinocerebellar ataxia type 40,,,,,,,C4518336,,616053,MONDO:0014475,spinocerebellar ataxia type 40,Spinocerebellar ataxia type 40 (disorder) | Spinocerebellar ataxia type 40
+BMGC_DS16624,BMG_DS063821,734021001,Spinocerebellar ataxia type 38 (disorder),,,,,,,C4518337,,615957,MONDO:0014417,spinocerebellar ataxia type 38,Spinocerebellar ataxia type 38 (disorder) | Spinocerebellar ataxia type 38
+BMGC_DS16625,BMG_DS063822,734022008,Wolfram-like syndrome,,,,,,,C4518338,,,,,Wolfram-like syndrome (disorder) | Wolfram-like syndrome
+BMGC_DS16626,BMG_DS063825,,,,,,,,,C4518341,,309300,MONDO:0010649,isolated congenital megalocornea,
+BMGC_DS16627,BMG_DS063827,734029004,Distal 22q11.2 microdeletion syndrome,,,,,,,C4518343,,,,,Distal 22q11.2 microdeletion syndrome (disorder) | Distal 22q11.2 microdeletion syndrome | Distal monosomy 22q11.2
+BMGC_DS16628,BMG_DS063828,734030009,12q15q21.1 microdeletion syndrome,,,,,,,C4518344,,,MONDO:0017334,12q15q21.1 microdeletion syndrome,12q15q21.1 microdeletion syndrome (disorder) | 12q15q21.1 microdeletion syndrome | Deletion 12q15q21.1 | Monosomy 12q15q21.1
+BMGC_DS16629,BMG_DS063830,,,,,,,,,C4518356,,,MONDO:0017886,MIT family translocation renal cell carcinoma,
+BMGC_DS16630,BMG_DS063883,733082001,Early-onset Lafora body disease,,,,,,,C4518574,,,,,Early-onset Lafora body disease (disorder) | Early-onset Lafora body disease
+BMGC_DS16631,BMG_DS063924,733195008,Epilepsy of infancy with migrating focal seizures,,,,,,,C4518639,,MTHU071843,MONDO:0100025,epilepsy of infancy with migrating focal seizures,Epilepsy of infancy with migrating focal seizures | Epilepsy of infancy with migrating focal seizures (disorder)
+BMGC_DS16632,BMG_DS063944,733337008,Noninfectious panuveitis,,,,,,,C4518725,,,,,Noninfectious panuveitis | Noninfectious panuveitis (disorder)
+BMGC_DS16633,BMG_DS063949,733418003,Joubert syndrome with Jeune asphyxiating thoracic dystrophy,,,,,,,C4518774,,,MONDO:0018342,Joubert syndrome with Jeune asphyxiating thoracic dystrophy,Joubert syndrome with JATD (Jeune asphyxiating thoracic dystrophy) | Joubert syndrome with Jeune asphyxiating thoracic dystrophy | Joubert syndrome with Jeune asphyxiating thoracic dystrophy (disorder)
+BMGC_DS16634,BMG_DS063951,733422008,Prion protein systemic amyloidosis,,,,,,,C4518776,,,MONDO:0018339,PrP systemic amyloidosis,Prion protein systemic amyloidosis (disorder) | Chronic diarrhoea with hereditary sensory and autonomic neuropathy | Prion protein systemic amyloidosis | PrP (prion protein) systemic amyloidosis | Chronic diarrhea with hereditary sensory and autonomic neuropathy
+BMGC_DS16635,BMG_DS063952,733447005,Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency,,,,,,,C4518781,,614665,MONDO:0013843,intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency,Meconium ileus due to guanylate cyclase 2C deficiency | Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency | Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency (disorder)
+BMGC_DS16636,BMG_DS063954,733450008,Carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency,,,,,,,C4518783,,,MONDO:0018349,MAN1B1-congenital disorder of glycosylation,Carbohydrate deficient glycoprotein syndrome type 2 due to deficiency of mannosidase alpha class 1B member 1 | MAN1B1-CDG - mannosidase alpha class 1B member 1 deficiency congenital disorder of glycosylation | Carbohydrate deficient glycoprotein syndrome type 2 due to deficiency of mannosidase alpha class 1B member 1 (disorder) | Congenital disorder of glycosylation type II due to MAN1B1 deficiency | Carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency
+BMGC_DS16637,BMG_DS063955,733452000,"Leukoencephalopathy, dystonia, motor neuropathy syndrome",,,,,,,C4518784,,,,,"Leukoencephalopathy, dystonia, motor neuropathy syndrome | Leukoencephalopathy, dystonia, motor neuropathy syndrome (disorder) | Leucoencephalopathy, dystonia, motor neuropathy syndrome"
+BMGC_DS16638,BMG_DS063956,733453005,"Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome",,,,,,,C4518785,,614748,MONDO:0013881,"epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome","Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome | Congenital ILNEB (interstitial lung disease, nephrotic syndrome, epidermolysis bullosa) syndrome | Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome (disorder) | Congenital nephrotic syndrome, epidermolysis bullosa, pulmonary disease syndrome"
+BMGC_DS16639,BMG_DS063958,733457006,Ehlers-Danlos and osteogenesis imperfecta syndrome,,,,,,,C4518787,,,MONDO:0016470,Ehlers-Danlos/osteogenesis imperfecta syndrome,Ehlers-Danlos and osteogenesis imperfecta syndrome | Ehlers-Danlos and osteogenesis imperfecta syndrome (disorder)
+BMGC_DS16640,BMG_DS063964,733489002,Distal myopathy with posterior leg and anterior hand involvement,,,,,,,C4518807,,,,,Distal myopathy with posterior leg and anterior hand involvement (disorder) | Distal myopathy with posterior leg and anterior hand involvement | Distal ABD-filaminopathy
+BMGC_DS16641,BMG_DS063967,733519008,17q12 microdeletion syndrome,,,,,,,C4518822,,,,,17q12 microdeletion syndrome | Monosomy 17q12 | 17q12 microdeletion syndrome (disorder)
+BMGC_DS16642,BMG_DS063969,733521003,Distal 16p11.2 microdeletion syndrome,,,,,DOID:0060398,"chromosome 16p11.2 deletion syndrome, 220-kb",C4518824,,,,,Distal 16p11.2 microdeletion syndrome | Distal 16p11.2 microdeletion syndrome (disorder) | Distal monosomy 16p11.2
+BMGC_DS16643,BMG_DS063971,,,,,,,,,C4518837,,,MONDO:0018433,acute myeloid leukemia with t(6;9)(p23;q34),
+BMGC_DS16644,BMG_DS063972,733599009,Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency,,,,,,,C4518838,,,,,Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency | Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency | Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency (disorder) | Adult-onset multiple mitochondrial DNA (deoxyribonucleic acid) deletion syndrome due to DGUOK (deoxyguanosine kinase) deficiency
+BMGC_DS16645,BMG_DS063973,733600007,Combined oxidative phosphorylation defect type 8,,,,,,,C4518839,,614096,MONDO:0013570,combined oxidative phosphorylation defect type 8,Combined oxidative phosphorylation defect type 8 (disorder) | Combined oxidative phosphorylation defect type 8 | COXPD8 - combined oxidative phosphorylation defect type 8
+BMGC_DS16646,BMG_DS064121,,,,,,,,,C4520840,,,MONDO:0859598,erythroleukemia,
+BMGC_DS16647,BMG_DS064123,254060000,Otospondylomegaepiphyseal dysplasia,,,,,,,C4520892,,,MONDO:0008975,otospondylomegaepiphyseal dysplasia,Otospondylomegaepiphyseal dysplasia | Otospondylomegaepiphyseal dysplasia (disorder)
+BMGC_DS16648,BMG_DS064125,,,,,,,,,C4520981,,,MONDO:0003996,basal ganglia disorder,
+BMGC_DS16649,BMG_DS064126,,,,,,,,,C4520983,,210500,MONDO:0100285,extrahepatic biliary atresia,
+BMGC_DS16650,BMG_DS064127,,Juvenile polyarthritis,,,,,,,C4521004,,MTHU056867,MONDO:0018456,polyarticular juvenile idiopathic arthritis,
+BMGC_DS16651,BMG_DS064129,,ACROMEGALY DUE TO PITUITARY ADENOMA 1,,,,,DOID:0112009,pituitary adenoma 1,C4521132,,102200,,,
+BMGC_DS16652,BMG_DS064134,,SPINOCEREBELLAR ATAXIA 44,,,,,DOID:0080286,spinocerebellar ataxia 44,C4521563,,604473;617691,MONDO:0033479,spinocerebellar ataxia 44,
+BMGC_DS16653,BMG_DS064135,,"FANCONI ANEMIA, COMPLEMENTATION GROUP W",,,,,DOID:0060978,Fanconi anemia complementation group W,C4521564,,617784;614151,MONDO:0044325,"Fanconi anemia, complementation group W",
+BMGC_DS16654,BMG_DS064136,,AUDITORY NEUROPATHY AND OPTIC ATROPHY,,,,,,,C4521678,,103270;617717,MONDO:0060582,auditory neuropathy-optic atrophy syndrome,
+BMGC_DS16655,BMG_DS064137,,"DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION",,,,,DOID:0080270,autosomal dominant nonsyndromic deafness 34,C4521680,,606416;617772,MONDO:0033261,"hearing loss, autosomal dominant 34, with or without inflammation",
+BMGC_DS16656,BMG_DS064140,,HELIX SYNDROME,,,,,,,C4522164,,617671;617579,MONDO:0060564,HELIX syndrome,
+BMGC_DS16657,BMG_DS064151,,,,,,,,,C4524190,,,MONDO:0018813,high grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement,
+BMGC_DS16658,BMG_DS064158,,,,,,,,,C4528210,,,MONDO:0850112,breast implant-associated anaplastic large cell lymphoma,
+BMGC_DS16659,BMG_DS064166,,,,,,,,,C4538355,,102200,MONDO:0007052,growth hormone secreting pituitary adenoma 1,
+BMGC_DS16660,BMG_DS064168,,MARSILI SYNDROME,,,,,DOID:0081075,Marsili syndrome,C4538468,,147430;617828,MONDO:0007828,"indifference to pain, congenital, autosomal dominant",
+BMGC_DS16661,BMG_DS064169,,"SYRINGOMYELIA, NONCOMMUNICATING ISOLATED",,,,,,,C4538540,,186700,MONDO:0008525,"syringomyelia, isolated",
+BMGC_DS16662,BMG_DS064170,,"COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY",,,,,,,C4538570,,226300;125240,,,
+BMGC_DS16663,BMG_DS064171,,DIENCEPHALIC-MESENCEPHALIC JUNCTION DYSPLASIA SYNDROME 1,,,,,,,C4538630,,251280;605622,MONDO:0009625,diencephalic-mesencephalic junction dysplasia syndrome 1,
+BMGC_DS16664,BMG_DS064173,,"GALLOWAY-MOWAT SYNDROME 2, X-LINKED",,,,,DOID:0080244,Galloway-Mowat syndrome 2,C4538784,,300060;301006,MONDO:0033006,"Galloway-Mowat syndrome 2, X-linked",
+BMGC_DS16665,BMG_DS064174,,,,,,,,,C4538788,,301008,MONDO:0030909,"intellectual disability, X-linked, syndromic, Houge type",
+BMGC_DS16666,BMG_DS064175,,"MYOPIA 26, X-LINKED, FEMALE-LIMITED",,,,,,,C4538795,,301010;301770,MONDO:0049221,"myopia 26, X-linked, female-limited",
+BMGC_DS16667,BMG_DS064179,,JOUBERT SYNDROME 34,,,,,,,C4539386,,611951;614175,MONDO:0800383,Joubert syndrome 34,
+BMGC_DS16668,BMG_DS064182,,,,,,,,,C4539685,,617540,MONDO:0054601,"pituitary adenoma 5, multiple types",
+BMGC_DS16669,BMG_DS064184,,MECKEL SYNDROME 13,,,,,DOID:0080253,Meckel syndrome 13,C4539714,,616183;617562,MONDO:0033044,Meckel syndrome 13,
+BMGC_DS16670,BMG_DS064185,,JOUBERT SYNDROME 29,,,,,DOID:0080253,Meckel syndrome 13,C4539715,,617562;616183,MONDO:0800372,Joubert syndrome 29,
+BMGC_DS16671,BMG_DS064186,,OROFACIODIGITAL SYNDROME XVI,,,,,DOID:0080254,orofaciodigital syndrome XVI,C4539729,,617563;616183,MONDO:0033045,orofaciodigital syndrome 16,
+BMGC_DS16672,BMG_DS064187,,,,,,,,,C4539754,,617571,MONDO:0033091,"ichthyosis, congenital, autosomal recessive 14",
+BMGC_DS16673,BMG_DS064188,,EXUDATIVE VITREORETINOPATHY 7,,,,,DOID:0080264,exudative vitreoretinopathy 7,C4539767,,617572;116806,MONDO:0033123,exudative vitreoretinopathy 7,
+BMGC_DS16674,BMG_DS064189,,,,,,,,,C4539772,,617574,MONDO:0033092,"ichthyosis, congenital, autosomal recessive 13",
+BMGC_DS16675,BMG_DS064190,,SPERMATOGENIC FAILURE 18,,,,,DOID:0070165,spermatogenic failure 18,C4539783,,617576;603332,MONDO:0054615,spermatogenic failure 18,
+BMGC_DS16676,BMG_DS064191,,"CILIARY DYSKINESIA, PRIMARY, 37",,,,,DOID:0080266,primary ciliary dyskinesia 37,C4539798,,603332;617577,MONDO:0033204,"ciliary dyskinesia, primary, 37",
+BMGC_DS16677,BMG_DS064192,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25",,,,,DOID:0080259,autosomal recessive spinocerebellar ataxia 25,C4539808,,604261;617584,MONDO:0033115,"spinocerebellar ataxia, autosomal recessive 25",
+BMGC_DS16678,BMG_DS064193,,IMMUNODEFICIENCY 53,,,,,DOID:0111992,immunodeficiency 53,C4539811,,617585;604758,MONDO:0054696,immunodeficiency 53,
+BMGC_DS16679,BMG_DS064194,,SPERMATOGENIC FAILURE 19,,,,,DOID:0070170,spermatogenic failure 19,C4539818,,617592;617558,MONDO:0054723,spermatogenic failure 19,
+BMGC_DS16680,BMG_DS064195,,SPERMATOGENIC FAILURE 20,,,,,DOID:0070166,spermatogenic failure 20,C4539824,,617593;617559,MONDO:0054724,spermatogenic failure 20,
+BMGC_DS16681,BMG_DS064196,,BIRK-LANDAU-PEREZ SYNDROME,,,,,,,C4539828,,604604;617595,MONDO:0044726,psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome,
+BMGC_DS16682,BMG_DS064197,,MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 3,,,,,DOID:0080689,mosaic variegated aneuploidy syndrome 3,C4539839,,617598;604507,MONDO:0054736,mosaic variegated aneuploidy syndrome 3,
+BMGC_DS16683,BMG_DS064198,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 55,,,,,DOID:0080283,developmental and epileptic encephalopathy 55,C4539843,,605938;617599,MONDO:0033364,"developmental and epileptic encephalopathy, 55",
+BMGC_DS16684,BMG_DS064199,,,,,,,,,C4539848,,617600,MONDO:0030910,"intellectual disability, autosomal dominant 45",
+BMGC_DS16685,BMG_DS064200,,,,,,,,,C4539851,,617601,MONDO:0030911,"intellectual disability, autosomal dominant 46",
+BMGC_DS16686,BMG_DS064201,,CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME,,,,,,,C4539857,,189980;617602,MONDO:0060532,congenital heart defects and skeletal malformations syndrome,
+BMGC_DS16687,BMG_DS064202,,"MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES",,,,,DOID:0081431,"microcephaly, short stature, and limb abnormalities",C4539873,,611428;617604,MONDO:0060533,"microcephaly, short stature, and limb abnormalities",
+BMGC_DS16688,BMG_DS064203,,"DEAFNESS, AUTOSOMAL DOMINANT 71",,,,,DOID:0080267,autosomal dominant nonsyndromic deafness 71,C4539881,,617605;612186,MONDO:0033258,"hearing loss, autosomal dominant 71",
+BMGC_DS16689,BMG_DS064204,,"DEAFNESS, AUTOSOMAL DOMINANT 72",,,,,DOID:0080268,autosomal dominant nonsyndromic deafness 72,C4539886,,617606;606107,MONDO:0033259,"hearing loss, autosomal dominant 72",
+BMGC_DS16690,BMG_DS064205,,"AMELOGENESIS IMPERFECTA, TYPE IIIB",,,,,DOID:0080243,amelogenesis imperfecta type 3B,C4539891,,617607;610912,MONDO:0021547,amelogenesis imperfecta type 3B,
+BMGC_DS16691,BMG_DS064206,,"NEPHROTIC SYNDROME, TYPE 15",,,,,DOID:0080271,nephrotic syndrome type 15,C4539896,,606382;617609,MONDO:0033262,nephrotic syndrome 15,
+BMGC_DS16692,BMG_DS064207,,POLYCYSTIC KIDNEY DISEASE 5,,,,,DOID:0080273,polycystic kidney disease 5,C4539903,,617570;617610,MONDO:0033281,polycystic kidney disease 5,
+BMGC_DS16693,BMG_DS064208,1279890001,Multiple mitochondrial dysfunctions syndrome type 5,,,,,,,C4539919,,617613,MONDO:0033282,multiple mitochondrial dysfunctions syndrome 5,Multiple mitochondrial dysfunctions syndrome type 5 (disorder) | ISCA1 deficiency | MMDS5 - multiple mitochondrial dysfunctions syndrome type 5 | ISCA1 (iron-sulfur cluster assembly 1) deficiency | Multiple mitochondrial dysfunctions syndrome type 5
+BMGC_DS16694,BMG_DS064209,,SKRABAN-DEARDORFF SYNDROME,,,,,,,C4539927,,617424;617616,MONDO:0054636,Skraban-Deardorff syndrome,
+BMGC_DS16695,BMG_DS064210,,JOUBERT SYNDROME 30,,,,,DOID:0080275,Joubert syndrome 30,C4539937,,617612;617622,MONDO:0033308,Joubert syndrome 30,
+BMGC_DS16696,BMG_DS064211,,"FIBROMATOSIS, GINGIVAL, 5",,,,,DOID:0080280,gingival fibromatosis 5,C4539942,,617626;600571,MONDO:0033493,"fibromatosis, gingival, 5",
+BMGC_DS16697,BMG_DS064212,,,,,,,,,C4539944,,617629,MONDO:0033312,schizophrenia 19,
+BMGC_DS16698,BMG_DS064213,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26",,,,,DOID:0080260,autosomal recessive spinocerebellar ataxia 26,C4539948,,617633;194360,MONDO:0033116,"spinocerebellar ataxia, autosomal recessive 26",
+BMGC_DS16699,BMG_DS064214,,,,,,,,,C4539951,,617635,MONDO:0030912,"intellectual disability, autosomal dominant 47",
+BMGC_DS16700,BMG_DS064215,,"DEAFNESS, AUTOSOMAL RECESSIVE 106",,,,,DOID:0080261,autosomal recessive nonsyndromic deafness 106,C4539954,,617637;614988,MONDO:0033198,"hearing loss, autosomal recessive 106",
+BMGC_DS16701,BMG_DS064216,,IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS,,,,,DOID:0111958,immunodeficiency 11B,C4539957,,607210;617638,MONDO:0054697,immunodeficiency 11b with atopic dermatitis,
+BMGC_DS16702,BMG_DS064217,,"DEAFNESS, AUTOSOMAL RECESSIVE 107",,,,,DOID:0080262,autosomal recessive nonsyndromic deafness 107,C4539964,,606962;617639,MONDO:0033199,"hearing loss, autosomal recessive 107",
+BMGC_DS16703,BMG_DS064218,,"CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY",,,,,DOID:0112359,"congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay",C4539968,,176310;617641,MONDO:0060549,"congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay",
+BMGC_DS16704,BMG_DS064219,,,,,,,,,C4539976,,617642,MONDO:0060550,"polydactyly, postaxial, type a7",
+BMGC_DS16705,BMG_DS064220,,"CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES",,,,,,,C4539985,,600150;617643,MONDO:0060551,"cerebellar atrophy, developmental delay, and seizures",
+BMGC_DS16706,BMG_DS064221,,SPERMATOGENIC FAILURE 21,,,,,DOID:0070163,spermatogenic failure 21,C4539991,,617644;602144,MONDO:0054725,spermatogenic failure 21,
+BMGC_DS16707,BMG_DS064222,,"DEAFNESS, AUTOSOMAL RECESSIVE 108",,,,,DOID:0080263,autosomal recessive nonsyndromic deafness 108,C4539997,,617654;602336,MONDO:0033200,"hearing loss, autosomal recessive 108",
+BMGC_DS16708,BMG_DS064223,,"VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1",,,,,,,C4540004,,617660;604521,MONDO:0060554,"vertebral, cardiac, renal, and limb defects syndrome 1",
+BMGC_DS16709,BMG_DS064224,,"VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2",,,,,,,C4540014,,605197;617661,MONDO:0060555,"vertebral, cardiac, renal, and limb defects syndrome 2",
+BMGC_DS16710,BMG_DS064225,1217372003,"Severe myopia, generalized joint laxity, short stature syndrome",,,,,,,C4540020,,617662,MONDO:0060556,"joint laxity, short stature, and myopia","Severe myopia, generalized joint laxity, short stature syndrome | Severe myopia, generalised joint laxity, short stature syndrome | Severe myopia, generalized joint laxity, short stature syndrome (disorder)"
+BMGC_DS16711,BMG_DS064226,,"DEAFNESS, AUTOSOMAL DOMINANT 73",,,,,DOID:0080269,autosomal dominant nonsyndromic deafness 73,C4540024,,617663;603317,MONDO:0033260,"hearing loss, autosomal dominant 73",
+BMGC_DS16712,BMG_DS064227,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32,,,,,DOID:0111492,combined oxidative phosphorylation deficiency 32,C4540029,,617664;611994,MONDO:0054654,combined oxidative phosphorylation deficiency 32,
+BMGC_DS16713,BMG_DS064228,,,,,,,,,C4540031,,,MONDO:0000732,combined oxidative phosphorylation deficiency,
+BMGC_DS16714,BMG_DS064229,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 56,,,,,DOID:0080282,developmental and epileptic encephalopathy 56,C4540034,,605356;617665,MONDO:0033365,"developmental and epileptic encephalopathy, 56",
+BMGC_DS16715,BMG_DS064230,,FRASER SYNDROME 2,,,,,DOID:0111407,Fraser syndrome 2,C4540036,,617666;608945,MONDO:0054738,Fraser syndrome 2,
+BMGC_DS16716,BMG_DS064231,,FRASER SYNDROME 3,,,,,DOID:0111406,Fraser syndrome 3,C4540040,,617667;604597,MONDO:0054739,Fraser syndrome 3,
+BMGC_DS16717,BMG_DS064232,,"ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES",,,,,,,C4540052,,617659;617668,MONDO:0060562,"encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities",
+BMGC_DS16718,BMG_DS064233,,"NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY",,,,,DOID:0070474,childhood-onset neurodegeneration with brain atrophy,C4540086,,617672;600673,MONDO:0044701,childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder,
+BMGC_DS16719,BMG_DS064234,1237514002,"Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome",,,,,,,C4540096,,617675,MONDO:0044714,mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome,"Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome | Mitochondrial myopathy, cerebellar atrophy, pigmentary retinopathy syndrome | Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome (disorder)"
+BMGC_DS16720,BMG_DS064235,,BLEPHAROCHEILODONTIC SYNDROME 2,,,,,DOID:0080346,blepharocheilodontic syndrome 2,C4540127,,617681;601045,MONDO:0040503,blepharocheilodontic syndrome 2,
+BMGC_DS16721,BMG_DS064236,1217382002,"Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome",,,,,,,C4540131,,617682,MONDO:0060568,Pilarowski-Bjornsson syndrome,"Pilarowski Bjornsson syndrome | Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome (disorder) | Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome"
+BMGC_DS16722,BMG_DS064237,,,,,,,,,C4540135,,617686,MONDO:0054665,"pituitary adenoma 3, multiple types",
+BMGC_DS16723,BMG_DS064238,,OVARIAN DYSGENESIS 5,,,,,DOID:0080497,ovarian dysgenesis 5,C4540141,,610224;617690,MONDO:0054666,ovarian dysgenesis 5,
+BMGC_DS16724,BMG_DS064239,,AL KAISSI SYNDROME,,,,,,,C4540156,,603464;617694,MONDO:0044324,Al Kaissi syndrome,
+BMGC_DS16725,BMG_DS064240,,,,,,,,,C4540164,,617695,MONDO:0054669,"pontocerebellar hypoplasia, type 11",
+BMGC_DS16726,BMG_DS064241,1222672002,3-methylglutaconic aciduria type 9,,,,,,,C4540171,,617698,MONDO:0044724,3-methylglutaconic aciduria type 9,"3-methylglutaconic aciduria, epilepsy, spasticity, severe intellectual disability syndrome | 3-methylglutaconic aciduria type 9 | 3-methylglutaconic aciduria type 9 (disorder)"
+BMGC_DS16727,BMG_DS064242,,SPERMATOGENIC FAILURE 22,,,,,DOID:0070177,spermatogenic failure 22,C4540179,,617706;617670,MONDO:0054726,spermatogenic failure 22,
+BMGC_DS16728,BMG_DS064243,,SPERMATOGENIC FAILURE 23,,,,,DOID:0070181,spermatogenic failure 23,C4540185,,617707;605792,MONDO:0054727,spermatogenic failure 23,
+BMGC_DS16729,BMG_DS064244,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ATAXIA, AND SEIZURES",,,,,,,C4540188,,607529;617709,MONDO:0060577,"neurodevelopmental disorder with microcephaly, ataxia, and seizures",
+BMGC_DS16730,BMG_DS064245,1260128008,WARS2-related combined oxidative phosphorylation defect,,,,,,,C4540192,,617710,MONDO:0060578,"neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures","WARS2-related combined oxidative phosphorylation defect | Tryptophanyl tRNA synthetase 2, mitochondrial-related combined oxidative phosphorylation defect (disorder) | Tryptophanyl tRNA synthetase 2, mitochondrial-related combined oxidative phosphorylation defect | Mitochondrial tryptophanyl-tRNA synthetase deficiency"
+BMGC_DS16731,BMG_DS064246,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 91,,,,,DOID:0080472,developmental and epileptic encephalopathy 91,C4540199,,617711;114105,MONDO:0020630,developmental and epileptic encephalopathy 91,
+BMGC_DS16732,BMG_DS064247,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 3,,,,,,,C4540205,,617712;182889,MONDO:0021574,oocyte maturation defect 3,
+BMGC_DS16733,BMG_DS064248,,,,,,,,,C4540209,,617713,MONDO:0054677,combined oxidative phosphorylation deficiency 33,
+BMGC_DS16734,BMG_DS064249,,IMMUNODEFICIENCY 71 WITH INFLAMMATORY DISEASE AND CONGENITAL THROMBOCYTOPENIA,,,,,DOID:0112004,immunodeficiency 71,C4540232,,604223;617718,MONDO:0060583,platelet abnormalities with eosinophilia and immune-mediated inflammatory disease,
+BMGC_DS16735,BMG_DS064250,,,,,,,,,C4540251,,617719,MONDO:0054680,"epiphyseal dysplasia, multiple, 7",
+BMGC_DS16736,BMG_DS064253,,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 9",,,,,DOID:0111212,autosomal dominant distal hereditary motor neuronopathy 9,C4540265,,191050;617721,MONDO:0060585,"neuronopathy, distal hereditary motor, type 9",
+BMGC_DS16737,BMG_DS064254,,GALLOWAY-MOWAT SYNDROME 3,,,,,DOID:0080245,Galloway-Mowat syndrome 3,C4540266,,617729;610107,MONDO:0033007,Galloway-Mowat syndrome 3,
+BMGC_DS16738,BMG_DS064255,,GALLOWAY-MOWAT SYNDROME 4,,,,,DOID:0080246,Galloway-Mowat syndrome 4,C4540270,,617730;608679,MONDO:0033008,Galloway-Mowat syndrome 4,
+BMGC_DS16739,BMG_DS064256,,GALLOWAY-MOWAT SYNDROME 5,,,,,DOID:0080247,Galloway-Mowat syndrome 5,C4540274,,617731;608680,MONDO:0033009,Galloway-Mowat syndrome 5,
+BMGC_DS16740,BMG_DS064257,,"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION",,,,,,,C4540277,,617732;615103,MONDO:0060589,"facial palsy, congenital, with ptosis and velopharyngeal dysfunction",
+BMGC_DS16741,BMG_DS064258,,,,,,,,,C4540284,,617743,MONDO:0021575,oocyte maturation defect 4,
+BMGC_DS16742,BMG_DS064259,,"IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA",,,,,,,C4540293,,600492;617744,MONDO:0060591,"immunodeficiency, developmental delay, and hypohomocysteinemia",
+BMGC_DS16743,BMG_DS064260,,SWEENEY-COX SYNDROME,,,,,DOID:0080538,Sweeney-Cox syndrome,C4540299,,601622;617746,MONDO:0060592,Sweeney-Cox syndrome,
+BMGC_DS16744,BMG_DS064261,,,,,,,,,C4540321,,617751,MONDO:0030913,"intellectual disability, autosomal dominant 48",
+BMGC_DS16745,BMG_DS064262,,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES,,,,,DOID:0070514,neurodevelopmental disorder with dysmorphic facies and distal limb anomalies,C4540327,,601819;617755,MONDO:0060596,neurodevelopmental disorder with dysmorphic facies and distal limb anomalies,
+BMGC_DS16746,BMG_DS064263,,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 5,,,,,DOID:0080251,erythrokeratodermia variabilis et progressiva 5,C4540331,,602765;617756,MONDO:0033015,erythrokeratodermia variabilis et progressiva 5,
+BMGC_DS16747,BMG_DS064264,,JOUBERT SYNDROME 32,,,,,DOID:0080278,Joubert syndrome 32,C4540342,,607035;617757,MONDO:0033309,Joubert syndrome 32,
+BMGC_DS16748,BMG_DS064265,,"MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION",,,,,DOID:0111221,centronuclear myopathy 6 with fiber-type disproportion,C4540345,,617760;609479,MONDO:0054695,"myopathy, centronuclear, 6, with fiber-type disproportion",
+BMGC_DS16749,BMG_DS064266,,JOUBERT SYNDROME 31,,,,,DOID:0080277,Joubert syndrome 31,C4540355,,617761;613446,MONDO:0033310,Joubert syndrome 31,
+BMGC_DS16750,BMG_DS064267,1237515001,Alkaline ceramidase 3 deficiency,,,,,,,C4540358,,617762,MONDO:0044718,alkaline ceramidase 3 deficiency,Leukodystrophy due to alkaline ceramidase 3 deficiency (disorder) | Alkaline ceramidase 3 deficiency | ACER3-related early childhood-onset progressive leukodystrophy | Leukodystrophy due to alkaline ceramidase 3 deficiency | ACER3-related early childhood-onset progressive leucodystrophy | Leucodystrophy due to alkaline ceramidase 3 deficiency
+BMGC_DS16751,BMG_DS064268,,"SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES",,,,,DOID:0081175,"short stature, hearing loss, retinitis pigmentosa, and distinctive facies",C4540367,,617763;602238,MONDO:0044634,retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome,
+BMGC_DS16752,BMG_DS064270,,"IMMUNODEFICIENCY, COMMON VARIABLE, 14",,,,,DOID:0081156,common variable immunodeficiency 14,C4540380,,617765;615332,MONDO:0054691,"immunodeficiency, common variable, 14",
+BMGC_DS16753,BMG_DS064271,,JOUBERT SYNDROME 33,,,,,DOID:0080279,Joubert syndrome 33,C4540389,,617767;607532,MONDO:0033311,Joubert syndrome 33,
+BMGC_DS16754,BMG_DS064272,,KLEEFSTRA SYNDROME 2,,,,,DOID:0080598,Kleefstra syndrome 2,C4540395,,606833;617768,MONDO:0054701,Kleefstra syndrome 2,
+BMGC_DS16755,BMG_DS064273,1279840000,Spinocerebellar ataxia type 45,,,,,,,C4540400,,617769,MONDO:0033480,spinocerebellar ataxia 45,Spinocerebellar ataxia type 45 (disorder) | Spinocerebellar ataxia type 45 | SCA45 - spinocerebellar ataxia type 45
+BMGC_DS16756,BMG_DS064274,1279839002,Spinocerebellar ataxia type 46,,,,,,,C4540404,,617770,MONDO:0033481,spinocerebellar ataxia 46,SCA46 - spinocerebellar ataxia type 46 | Spinocerebellar ataxia type 46 (disorder) | Spinocerebellar ataxia type 46
+BMGC_DS16757,BMG_DS064275,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 57,,,,,DOID:0080284,developmental and epileptic encephalopathy 57,C4540411,,610044;617771,MONDO:0033366,"developmental and epileptic encephalopathy, 57",
+BMGC_DS16758,BMG_DS064276,,,,,,,,,C4540424,,617773,MONDO:0030915,"intellectual disability, autosomal recessive 61",
+BMGC_DS16759,BMG_DS064277,,COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA,,,,,,,C4540434,,617780,MONDO:0060611,combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia,
+BMGC_DS16760,BMG_DS064278,,RETINITIS PIGMENTOSA 80,,,,,,,C4540439,,617781;614620,MONDO:0054708,retinitis pigmentosa 80,
+BMGC_DS16761,BMG_DS064279,,"NEPHROTIC SYNDROME, TYPE 16",,,,,DOID:0080272,nephrotic syndrome type 16,C4540453,,617783;614610,MONDO:0033280,nephrotic syndrome 16,
+BMGC_DS16762,BMG_DS064280,,,,,,,,,C4540470,,617787,MONDO:0030916,"intellectual disability, autosomal dominant 50",
+BMGC_DS16763,BMG_DS064281,,,,,,,,,C4540474,,617788,MONDO:0030917,"intellectual disability, autosomal dominant 51",
+BMGC_DS16764,BMG_DS064282,,,,,,,,,C4540478,,617796,MONDO:0030918,"intellectual disability, autosomal dominant 52",
+BMGC_DS16765,BMG_DS064283,,,,,,,,,C4540481,,617798,MONDO:0030919,"intellectual disability, autosomal dominant 53",
+BMGC_DS16766,BMG_DS064284,,,,,,,,,C4540484,,617799,MONDO:0030920,"intellectual disability, autosomal dominant 54",
+BMGC_DS16767,BMG_DS064285,,"MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE",,,,,DOID:0070281,primary autosomal recessive microcephaly 19,C4540488,,617800;606990,MONDO:0054716,"microcephaly 19, primary, autosomal recessive",
+BMGC_DS16768,BMG_DS064286,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY",,,,,,,C4540493,,192150;617802,MONDO:0060621,"neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy",
+BMGC_DS16769,BMG_DS064287,,,,,,,,,C4540496,,617804,MONDO:0060622,neurodevelopmental disorder with severe motor impairment and absent language,
+BMGC_DS16770,BMG_DS064288,,,,,,,,,C4540497,,617805,MONDO:0024520,renal hypodysplasia/aplasia 3,
+BMGC_DS16771,BMG_DS064289,,"NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER",,,,,,,C4540498,,604198;617807,MONDO:0060624,"neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter",
+BMGC_DS16772,BMG_DS064290,,COFFIN-SIRIS SYNDROME 6,,,,,DOID:0080297,Coffin-Siris syndrome 6,C4540499,,617808;609539,MONDO:0033492,Coffin-Siris syndrome 6,
+BMGC_DS16773,BMG_DS064291,,,,,,,,,C4540511,,617809,MONDO:0054722,geleophysic dysplasia 3,
+BMGC_DS16774,BMG_DS064292,1217381009,"Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome",,,,,,,C4540520,,617810,MONDO:0060627,glycosylphosphatidylinositol biosynthesis defect 15,"Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome | Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome (disorder) | GPAA1-related biosynthesis defect | Glycosylphosphatidylinositol anchor attachment 1-related biosynthesis defect"
+BMGC_DS16775,BMG_DS064293,,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 16,,,,,DOID:0081223,glycosylphosphatidylinositol biosynthesis defect 16,C4540521,,601730;617816,MONDO:0040500,glycosylphosphatidylinositol biosynthesis defect 16,
+BMGC_DS16776,BMG_DS064294,,GLUCOCORTICOID DEFICIENCY 5,,,,,,,C4540522,,606448;617825,MONDO:0040502,glucocorticoid deficiency 5,
+BMGC_DS16777,BMG_DS064299,,"SHORT STATURE AND ADVANCED BONE AGE, WITH EARLY-ONSET OSTEOARTHRITIS",,,,,,,C4540542,,155760,,,
+BMGC_DS16778,BMG_DS064302,,RENI SYNDROME,,,,,DOID:0080265,nephrotic syndrome type 14,C4540559,,617575;603729,MONDO:0033203,nephrotic syndrome 14,
+BMGC_DS16779,BMG_DS064305,,POLYCYSTIC KIDNEY DISEASE 4,,,,,,,C4540575,,606702;263200,MONDO:0033004,polycystic kidney disease 4,
+BMGC_DS16780,BMG_DS064510,735438000,Disorder of neutrophil chemotaxis,,,,,,,C4543735,,,,,Disorder of neutrophil chemotaxis (disorder) | Disorder of neutrophil chemotaxis
+BMGC_DS16781,BMG_DS064519,735451005,Chronic viral hepatitis D,,,,,,,C4543747,,,,,Chronic infection caused by Hepatitis D virus (disorder) | Chronic viral hepatitis D | Chronic infection caused by Hepatitis D virus
+BMGC_DS16782,BMG_DS064618,735676003,Narcolepsy type 1,,,,,,,C4543926,,,,,Narcolepsy type 1 (disorder) | Narcolepsy type 1
+BMGC_DS16783,BMG_DS064824,,Chronic Primary Pain,Chronic Pain,,,,,,C4545041,D059350,,,,
+BMGC_DS16784,BMG_DS064898,737582007,Hemiparkinsonism hemiatrophy syndrome,,,,,,,C4545231,,,MONDO:0017636,hemiparkinsonism-hemiatrophy syndrome,Hemiparkinsonism hemiatrophy syndrome (disorder) | Hemiparkinsonism hemiatrophy syndrome
+BMGC_DS16785,BMG_DS064942,,,,,,,,,C4545381,,,MONDO:0015689,myeloid neoplasm associated with PDGFRA rearrangement,
+BMGC_DS16786,BMG_DS064976,,Congenital Zika Syndrome,Zika Virus Infection,,,,DOID:0060478,Zika fever,C4546023,D000071243,,MONDO:0000890,Zika virus congenital syndrome,
+BMGC_DS16787,BMG_DS065013,,,,,,,,,C4546092,,,MONDO:0017117,congenital non-communicating hydrocephalus,
+BMGC_DS16788,BMG_DS065225,,Seckel syndrome 1,,,,,DOID:0070007,Seckel syndrome 1,C4551474,C537533,210600,MONDO:0008869,Seckel syndrome 1,
+BMGC_DS16789,BMG_DS065226,,"ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1",,,,,DOID:0060766,autosomal dominant Robinow syndrome 1,C4551475,,164975;180700,MONDO:0024455,autosomal dominant Robinow syndrome 1,
+BMGC_DS16790,BMG_DS065227,,NEU-LAXOVA SYNDROME 1,,,,,DOID:0080076,Neu-Laxova syndrome 1,C4551478,,256520;606879,MONDO:0009736,Neu-Laxova syndrome 1,
+BMGC_DS16791,BMG_DS065228,,"Schwartz-Jampel Syndrome, Type 1",Osteochondrodysplasias,,,,,,C4551479,D010009,255800,MONDO:0100435,Schwartz-Jampel syndrome type 1,
+BMGC_DS16792,BMG_DS065229,,FRASER SYNDROME 1,,,,,DOID:0111405,Fraser syndrome 1,C4551480,,607830;219000,MONDO:0054737,Fraser syndrome 1,
+BMGC_DS16793,BMG_DS065230,,TOWNES-BROCKS SYNDROME 1,,,,,,,C4551481,,107480,MONDO:0054581,Townes-Brocks syndrome 1,
+BMGC_DS16794,BMG_DS065231,,Adams-Oliver syndrome 1,,,,,,,C4551482,C538225,100300,MONDO:0024506,Adams-Oliver syndrome 1,
+BMGC_DS16795,BMG_DS065232,,SCLEROSTEOSIS 1,,,,,,,C4551483,,269500,MONDO:0010016,sclerosteosis 1,
+BMGC_DS16796,BMG_DS065233,,"LEOPARD Syndrome, 1",LEOPARD Syndrome,,,,,,C4551484,D044542,151100,MONDO:0100082,LEOPARD syndrome 1,
+BMGC_DS16797,BMG_DS065234,,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1,,,,,DOID:0111195,erythrokeratodermia variabilis et progressiva 1,C4551486,,133200;603324,MONDO:0033010,erythrokeratodermia variabilis et progressiva 1,
+BMGC_DS16798,BMG_DS065235,,,,,,,,,C4551488,,192100,MONDO:0008637,bifid uvula,
+BMGC_DS16799,BMG_DS065236,,,,,,,,,C4551493,,,MONDO:0010029,situs inversus,
+BMGC_DS16800,BMG_DS065238,,"Hypophosphatemic Rickets, Autosomal Recessive, 1",,,,,,,C4551495,C562792,241520,MONDO:0009430,"hypophosphatemic rickets, autosomal recessive, 1",
+BMGC_DS16801,BMG_DS065239,,"Hyperuricemic Nephropathy, Familial Juvenile 1",,,,,,,C4551496,C537696,609886;162000;603860,MONDO:0008073,familial juvenile hyperuricemic nephropathy type 1,
+BMGC_DS16802,BMG_DS065242,,"EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1",,,,,DOID:0080986,Ehlers-Danlos syndrome periodontal type 1,C4551499,,130080;613785,MONDO:0020684,"Ehlers-Danlos syndrome, periodontal type 1",
+BMGC_DS16803,BMG_DS065243,,"Amyloid Polyneuropathy, Iowa Type","Amyloid Neuropathies, Familial",,,,,,C4551500,D028227,620657,MONDO:0971008,"amyloidosis, hereditary systemic 3",
+BMGC_DS16804,BMG_DS065244,,"AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1",,,,,DOID:0080930,primary localized cutaneous amyloidosis 1,C4551501,,105250;601743,MONDO:0024522,"amyloidosis, primary localized cutaneous, 1",
+BMGC_DS16805,BMG_DS065245,,HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 1,,,,,DOID:0070433,hyperphosphatasia with impaired intellectual development syndrome 1,C4551502,,610274;239300,MONDO:0009398,hyperphosphatasia with intellectual disability syndrome 1,
+BMGC_DS16806,BMG_DS065246,,FANCONI RENOTUBULAR SYNDROME 1,,,,,DOID:0080757,Fanconi renotubular syndrome 1,C4551503,,134600;602360,MONDO:0024525,Fanconi renotubular syndrome 1,
+BMGC_DS16807,BMG_DS065247,,Oculocutaneous albinism type 1A,,,,,,,C4551504,C537728,203100,MONDO:0008745,oculocutaneous albinism type 1A,
+BMGC_DS16808,BMG_DS065248,13144005,Methylcrotonyl-CoA carboxylase deficiency,,,,,,,C4551505,,,MONDO:0018950,3-methylcrotonyl-CoA carboxylase deficiency,"Methylcrotonyl-CoA carboxylase deficiency | BMCC deficiency | MCC deficiency | beta-Methylcrotonylglycinuria, type 1 | 3-Methylcrotonyl-CoA carboxylase deficiency | Methylcrotonyl-coenzyme A carboxylase deficiency (disorder) | Methylcrotonyl-coenzyme A carboxylase deficiency"
+BMGC_DS16809,BMG_DS065249,,Paroxysmal Nonkinesigenic Dyskinesia 1,,,,,,,C4551506,C537181,118800,MONDO:0700089,paroxysmal nonkinesigenic dyskinesia 1,
+BMGC_DS16810,BMG_DS065250,2065009,Dominant hereditary optic atrophy,,,,,,,C4551508,,,MONDO:0020250,autosomal dominant optic atrophy,Dominant hereditary optic atrophy | Dominant hereditary optic atrophy (disorder) | Autosomal dominant optic atrophy
+BMGC_DS16811,BMG_DS065251,,Jervell And Lange-Nielsen Syndrome 1,Jervell-Lange Nielsen Syndrome,,,,,,C4551509,D029593,220400,MONDO:0024540,Jervell and Lange-Nielsen syndrome 1,
+BMGC_DS16812,BMG_DS065252,,CARPENTER SYNDROME 1,,,,,,,C4551510,,201000,MONDO:0008710,RAB23-related Carpenter syndrome,
+BMGC_DS16813,BMG_DS065253,62677000;48983004,X-linked sideroblastic anemia,,,,,,,C4551511,C536761,300751,MONDO:0020721,X-linked sideroblastic anemia 1,Hereditary sideroblastic anemia | Erythroid 5-aminolaevulinate synthetase deficiency | X-linked sideroblastic anaemia | X chromosome-linked sideroblastic anaemia | Hereditary sideroblastic anaemia | Erythroid 5-aminolevulinate synthetase deficiency | X chromosome-linked sideroblastic anemia | X-linked sideroblastic anemia | Hereditary sideroblastic anemia (disorder) | X chromosome-linked sideroblastic anemia | X chromosome-linked sideroblastic anaemia | X chromosome-linked sideroblastic anemia (disorder) | X-linked sideroblastic anemia | X-linked sideroblastic anaemia
+BMGC_DS16814,BMG_DS065254,,DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA,,,,,DOID:0111576,dehydrated hereditary stomatocytosis 1,C4551512,,194380,MONDO:0008689,dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema,
+BMGC_DS16815,BMG_DS065255,,"Hemophagocytic Lymphohistiocytosis, Familial, 1","Lymphohistiocytosis, Hemophagocytic",,,,,,C4551514,D051359,267700,MONDO:0009974,familial hemophagocytic lymphohistiocytosis type 1,
+BMGC_DS16816,BMG_DS065256,11361009;72470008;238928005,Chilblain lupus erythematosus,,,,,,,C4551515,,,MONDO:0019557,chilblain lupus,"Chilblain lupus erythematosus | Chilblain lupus erythematosus (disorder) | Sarcoidosis, lupus pernio type | Lupus pernio | Sarcoidosis, lupus pernio type (disorder)"
+BMGC_DS16817,BMG_DS065257,,Abducens Nerve Palsy,Abducens Nerve Diseases,,,,,,C4551519,D020434,100200,MONDO:0007033,abducens nerve palsy,
+BMGC_DS16818,BMG_DS065258,,Focal segmental glomerulosclerosis 1,,,,,,,C4551527,C538457,603278,MONDO:0011303,focal segmental glomerulosclerosis 1,
+BMGC_DS16819,BMG_DS065260,,"EPILEPSY, HOT WATER, 1",,,,,DOID:0081106,hot water epilepsy 1,C4551550,,613339,MONDO:0024508,"epilepsy, hot water, 1",
+BMGC_DS16820,BMG_DS065261,230552007,X-linked hereditary motor and sensory neuropathy,,,,,,,C4551551,,,MONDO:0018994,Charcot-Marie-Tooth disease type X,X-linked hereditary motor and sensory neuropathy | X-linked hereditary motor and sensory neuropathy (disorder) | X-linked Charcot-Marie-Tooth disease
+BMGC_DS16821,BMG_DS065262,,"CEREBELLAR ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSEQUILIBRIUM SYNDROME 1",,,,,DOID:0070556,"cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 1",C4551552,,192977;224050,MONDO:0024542,"cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1",
+BMGC_DS16822,BMG_DS065263,,SPECIFIC GRANULE DEFICIENCY 1,,,,,,,C4551556,,245480;600749,MONDO:0044207,specific granule deficiency 1,
+BMGC_DS16823,BMG_DS065264,,IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1,,,,,,,C4551557,,242860;602900,MONDO:0009454,immunodeficiency-centromeric instability-facial anomalies syndrome 1,
+BMGC_DS16824,BMG_DS065265,,"Fibromatosis, Gingival, Type 1",,,,,,,C4551558,C562884,135300,MONDO:0007609,"fibromatosis, gingival, 1",
+BMGC_DS16825,BMG_DS065266,,Senior-Loken Syndrome 1,,,,,DOID:0050576,Senior-Loken syndrome,C4551559,C537580,266900,MONDO:0009962,Senior-Loken syndrome 1,
+BMGC_DS16826,BMG_DS065267,,"AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 1",,,,,,,C4551562,,608805,MONDO:0054550,"avascular necrosis of femoral head, primary, 1",
+BMGC_DS16827,BMG_DS065268,,,,,,,,,C4551563,,,MONDO:0001149,microcephaly,
+BMGC_DS16828,BMG_DS065270,,Joubert syndrome 1,,,,,,,C4551568,C536293,213300,MONDO:0008944,Joubert syndrome 1,
+BMGC_DS16829,BMG_DS065271,254093009;239034008,Cranioectodermal dysplasia,,,,,,,C4551571,,,MONDO:0009032,cranioectodermal dysplasia,Cranioectodermal dysplasia | Sensenbrenner's syndrome | Cranioectodermal dysplasia (disorder) | Cranioectodermal dysplasia | Cranioectodermal dysplasia (disorder)
+BMGC_DS16830,BMG_DS065272,,"MYOFIBROMATOSIS, INFANTILE, 1",,,,,,,C4551572,,228550;173410,MONDO:0009227,"myofibromatosis, infantile, 1",
+BMGC_DS16831,BMG_DS065273,,UNCOMBABLE HAIR SYNDROME 1,,,,,,,C4551573,,606755;191480,MONDO:0020736,uncombable hair syndrome 1,
+BMGC_DS16832,BMG_DS065274,,Cerebral cortical atrophy,,,,,,,C4551583,,MTHU015450,,,
+BMGC_DS16833,BMG_DS065275,,Brain atrophy,,,,,,,C4551584,,MTHU005283,,,
+BMGC_DS16834,BMG_DS065276,,"ESOPHAGITIS, EOSINOPHILIC, 1",,,,,,,C4551589,,610247,MONDO:0012451,"esophagitis, eosinophilic, 1",
+BMGC_DS16835,BMG_DS065277,236478009,Familial renal hypouricemia,,,,,,,C4551590,,,MONDO:0009071,hereditary renal hypouricemia,Dalmatian hypouricaemia | Familial renal hypouricaemia | Dalmatian hypouricemia | Familial renal hypouricemia | Familial renal hypouricemia (disorder)
+BMGC_DS16836,BMG_DS065278,,"SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1",,,,,DOID:0112242,congenital symmetric circumferential skin creases 1,C4551592,,156610;191130,MONDO:0020738,multiple benign circumferential skin creases on limbs 1,
+BMGC_DS16837,BMG_DS065280,,"Biliary Cirrhosis, Primary, 1","Liver Cirrhosis, Biliary",,,,,,C4551595,D008105,109720,MONDO:0007193,primary biliary cholangitis 1,
+BMGC_DS16838,BMG_DS065281,,Noonan Syndrome 1,Noonan Syndrome,,,,,,C4551602,D009634,163950,MONDO:0008104,Noonan syndrome 1,
+BMGC_DS16839,BMG_DS065282,,"EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1",,,,,DOID:0080727,Ehlers-Danlos syndrome arthrochalasia type 1,C4551623,,130060;120150,MONDO:0007525,"Ehlers-Danlos syndrome, arthrochalasia type",
+BMGC_DS16840,BMG_DS065283,,Idiopathic basal ganglia calcification 1,,,,,,,C4551624,C536275,606656;213600,MONDO:0024538;MONDO:0008947,"basal ganglia calcification, idiopathic, 1 | bilateral striopallidodentate calcinosis",
+BMGC_DS16841,BMG_DS065284,,,,,,,,,C4551625,,,MONDO:0016557,leukonychia totalis,
+BMGC_DS16842,BMG_DS065285,417672002,Granulocytopenic disorder,,,,,,,C4551627,,,,,Granulocytopenic disorder (disorder) | Granulocytopenic disorder | Granulocytopenia
+BMGC_DS16843,BMG_DS065286,,Ichthyosis Congenita I,"Ichthyosis, Lamellar",,,,,,C4551630,D017490,242300,MONDO:0009441,autosomal recessive congenital ichthyosis 1,
+BMGC_DS16844,BMG_DS065287,233870001;15974001,Recurrent pancreatitis,,,,,,,C4551632,,,,,Recurrent pancreatitis | Recurrent pancreatitis (disorder) | Chronic pancreatitis | Chronic pancreatitis (disorder)
+BMGC_DS16845,BMG_DS065291,,"Erythrocytosis familial, 1",,,,,,,C4551637,C536842,133100,MONDO:0007572,primary familial polycythemia due to EPO receptor mutation,
+BMGC_DS16846,BMG_DS065292,,Romano-Ward Syndrome,Romano-Ward Syndrome,,,,,,C4551647,D029597,192500,MONDO:0100316,long QT syndrome 1,
+BMGC_DS16847,BMG_DS065293,,,,,,,,,C4551649,,,MONDO:0000158,developmental dysplasia of the hip,
+BMGC_DS16848,BMG_DS065294,,Esophageal Stricture,Esophageal Stenosis,,,,,,C4551650,D004940,,,,
+BMGC_DS16849,BMG_DS065296,28998008,Intraretinal hemorrhage,,,,,,,C4551659,,,,,Retinal hemorrhage | Retinal haemorrhage | Retinal hemorrhage (disorder) | Retinal haemorrhages | Retinal hemorrhages | Intraretinal haemorrhage | Intraretinal hemorrhage
+BMGC_DS16850,BMG_DS065297,41841004,Refractory sideroblastic anemia,,,,,,,C4551661,,MTHU038362,,,Sideroblastic anemia | Primary sideroblastic anemia | Refractory sideroblastic anemia | Sideroachrestic anemia | Primary sideroblastic anaemia | Sideroachrestic anaemia | Refractory sideroblastic anaemia | Sideroblastic anaemia | Sideroblastic anemia (disorder)
+BMGC_DS16851,BMG_DS065299,,"Keratoderma, Palmoplantar","Keratoderma, Palmoplantar",,,,,,C4551675,D007645,,,,
+BMGC_DS16852,BMG_DS065301,,"HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1",,,,,,,C4551679,,259100;601688,MONDO:0024546,"hypertrophic osteoarthropathy, primary, autosomal recessive, 1",
+BMGC_DS16853,BMG_DS065303,,"Periodontitis, Aggressive, 1",Aggressive Periodontitis,,,,,,C4551681,D010520,170650,MONDO:0008226,"periodontitis, aggressive 1",
+BMGC_DS16854,BMG_DS065304,,,,,,,,,C4551683,,,MONDO:0004974,adrenal gland pheochromocytoma,
+BMGC_DS16855,BMG_DS065307,,Sleep-Disordered Breathing,Sleep Apnea Syndromes,,,,,,C4551689,D012891,,,,
+BMGC_DS16856,BMG_DS065308,,,,,,,,,C4551691,,,MONDO:0002127,urethral stricture,
+BMGC_DS16857,BMG_DS065309,,Wolfram Syndrome 1,Wolfram Syndrome,,,,,,C4551693,D014929,222300,MONDO:0009101,Wolfram syndrome 1,
+BMGC_DS16858,BMG_DS065310,,Branchiootorenal Syndrome 1,Branchio-Oto-Renal Syndrome,,,,,,C4551702,D019280,113650,MONDO:0007236,branchiootorenal syndrome 1,
+BMGC_DS16859,BMG_DS065311,,Rod-Cone Dystrophy,Cone-Rod Dystrophies,,,,,,C4551714,D000071700,,,,
+BMGC_DS16860,BMG_DS065312,,Pigmentary retinopathy,,,,,,,C4551715,,MTHU000153,,,
+BMGC_DS16861,BMG_DS065313,,Primary Ciliary Dyskinesia,Ciliary Motility Disorders,,,,,,C4551720,D002925,,,,
+BMGC_DS16862,BMG_DS065314,,PERRAULT SYNDROME 1,,,,,,,C4551721,,601860;233400,MONDO:0009300,Perrault syndrome 1,
+BMGC_DS16863,BMG_DS065315,,Esodeviation,Esotropia,,,,,,C4551734,D004948,,,,
+BMGC_DS16864,BMG_DS065317,,"CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1",,,,,,,C4551768,,125310;600276,MONDO:0000914,"cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1",
+BMGC_DS16865,BMG_DS065318,,"Seizures, Benign Familial Infantile, 1","Epilepsy, Benign Neonatal",,,,,,C4551769,D020936,601764,MONDO:0042499,benign familial neonatal-infantile seizures 1,
+BMGC_DS16866,BMG_DS065319,724207001,Kleefstra syndrome,,,,,,,C4551771,,,MONDO:0012455,Kleefstra syndrome,Kleefstra syndrome (disorder) | Kleefstra syndrome
+BMGC_DS16867,BMG_DS065320,,GALLOWAY-MOWAT SYNDROME 1,,,,,DOID:0060364,Galloway-Mowat syndrome 1,C4551772,,251300;616144,MONDO:0033005,Galloway-Mowat syndrome 1,
+BMGC_DS16868,BMG_DS065321,,ZIMMERMANN-LABAND SYNDROME 1,,,,,,,C4551773,,603305;135500,MONDO:0024526,Zimmermann-Laband syndrome 1,
+BMGC_DS16869,BMG_DS065322,,,,,,,,,C4551774,,164280,MONDO:0008115,Feingold syndrome type 1,
+BMGC_DS16870,BMG_DS065323,,"Knobloch Syndrome, Type I",,,,,,,C4551775,C537209,267750,MONDO:0800167,Knobloch syndrome 1,
+BMGC_DS16871,BMG_DS065324,,RITSCHER-SCHINZEL SYNDROME 1,,,,,DOID:0060571,Ritscher-Schinzel syndrome 1,C4551776,,220210;610657,MONDO:0009073,Ritscher-Schinzel syndrome 1,
+BMGC_DS16872,BMG_DS065326,,Brugada Syndrome 1,Brugada Syndrome,,,,,,C4551804,D053840,601144,MONDO:0011001,Brugada syndrome 1,
+BMGC_DS16873,BMG_DS065327,,Oguchi Disease 1,,,,,,,C4551824,C537743,258100,MONDO:0009775,Oguchi disease-1,
+BMGC_DS16874,BMG_DS065328,,Megaloblastic Anemia 1,,,,,,,C4551825,C538556,,MONDO:0009853,Imerslund-Grasbeck syndrome,
+BMGC_DS16875,BMG_DS065329,,Deafness-symphalangism syndrome of Herrmann,,,,,,,C4551826,C536943,,,,
+BMGC_DS16876,BMG_DS065330,193225000;44292004;73297009,Hereditary progressive muscular dystrophy,,,,,,,C4551827,,,MONDO:0016106,progressive muscular dystrophy,Hereditary progressive muscular dystrophy | Hereditary progressive muscular dystrophy (disorder) | Muscular dystrophy | MD - Muscular dystrophy | Progressive muscular dystrophy | PMD - Progressive muscular dystrophy | Muscular dystrophy (disorder)
+BMGC_DS16877,BMG_DS065331,,Median Nerve Entrapment,Median Neuropathy,,,,,,C4551829,D020423,,,,
+BMGC_DS16878,BMG_DS065333,,Cornelia de Lange Syndrome 1,De Lange Syndrome,,,,,,C4551851,D003635,122470,MONDO:0007387,Cornelia de Lange syndrome 1,
+BMGC_DS16879,BMG_DS065334,,HYPOPLASTIC LEFT HEART SYNDROME 1,,,,,,,C4551854,,241550,MONDO:0009433,hypoplastic left heart syndrome 1,
+BMGC_DS16880,BMG_DS065335,,Asphyxiating Thoracic Dystrophy 1,,,,,,,C4551856,C537571,208500,MONDO:0008831,asphyxiating thoracic dystrophy 1,
+BMGC_DS16881,BMG_DS065336,,Vesicoureteral Reflux 1,Vesico-Ureteral Reflux,,,,,,C4551858,D014718,193000,MONDO:0008653,vesicoureteral reflux 1,
+BMGC_DS16882,BMG_DS065337,,RUBINSTEIN-TAYBI SYNDROME 1,,,,,,,C4551859,,180849;600140,MONDO:0008393,Rubinstein-Taybi syndrome due to CREBBP mutations,
+BMGC_DS16883,BMG_DS065338,240062007,Ullrich congenital muscular dystrophy,,,,,,,C4551860,,,MONDO:0000355,Ullrich congenital muscular dystrophy,Congenita hypotonic - sclerotic muscular dystrophy | Ullrich congenital muscular dystrophy | Ullrich congenital muscular dystrophy (disorder)
+BMGC_DS16884,BMG_DS065339,,"Telangiectasia, Hereditary Hemorrhagic, Type 1","Telangiectasia, Hereditary Hemorrhagic",,,,,,C4551861,D013683,187300,MONDO:0008535,"telangiectasia, hereditary hemorrhagic, type 1",
+BMGC_DS16885,BMG_DS065340,,"Ophthalmoplegia, Progressive Supranuclear","Supranuclear Palsy, Progressive",,,,,,C4551862,D013494,,,,
+BMGC_DS16886,BMG_DS065341,,"Supranuclear Palsy, Progressive, 1","Supranuclear Palsy, Progressive",,,,,,C4551863,D013494,601104,MONDO:0010997,"supranuclear palsy, progressive, 1",
+BMGC_DS16887,BMG_DS065342,,VAN DER WOUDE SYNDROME 1,,,,,,,C4551864,,119300;607199,MONDO:0007333,van der Woude syndrome 1,
+BMGC_DS16888,BMG_DS065343,,"Choroidal Dystrophy, Central Areolar 1",,,,,,,C4551884,C535358,215500,MONDO:0024539,"choroidal dystrophy, central areolar, 1",
+BMGC_DS16889,BMG_DS065345,,Familial Cold Autoinflammatory Syndrome 1,Cryopyrin-Associated Periodic Syndromes,,,,,,C4551895,D056587,120100,MONDO:0007349,familial cold autoinflammatory syndrome 1,
+BMGC_DS16890,BMG_DS065346,,"Cholestasis, progressive familial intrahepatic 1",,,,,DOID:0070226,progressive familial intrahepatic cholestasis 1,C4551898,C535933,211600,MONDO:0008892,progressive familial intrahepatic cholestasis type 1,
+BMGC_DS16891,BMG_DS065347,,Summerskill syndrome,,,,,DOID:0070226,progressive familial intrahepatic cholestasis 1,C4551899,C535933,243300,MONDO:0009469,benign recurrent intrahepatic cholestasis type 1,
+BMGC_DS16892,BMG_DS065348,,OTOSCLEROSIS 1,,,,,DOID:0060920,otosclerosis 1,C4551901,,166800,MONDO:0008164,otosclerosis 1,
+BMGC_DS16893,BMG_DS065349,,"Craniosynostosis, Type 1",Craniosynostoses,,,,,,C4551902,D003398,123100,MONDO:0007399,TWIST1-related craniosynostosis,
+BMGC_DS16894,BMG_DS065350,111323005,Total anomalous pulmonary venous return,,,,,,,C4551903,,MTHU019108;106700,MONDO:0007130,congenital total pulmonary venous return anomaly,Total anomalous pulmonary venous return | Total anomalous pulmonary venous return (disorder) | Total anomalous pulmonary venous connection | TAPVC - total anomalous pulmonary venous connection | TAPVD - total anomalous pulmonary venous drainage | TAPVR - total anomalous pulmonary venous return
+BMGC_DS16895,BMG_DS065352,,"Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus",Kartagener Syndrome,,,,DOID:0050144,Kartagener syndrome,C4551906,D007619,244400,MONDO:0009484,primary ciliary dyskinesia 1,
+BMGC_DS16896,BMG_DS065353,,Acute Inflammatory Demyelinating Polyneuropathy,Guillain-Barre Syndrome,,,,,,C4551910,D020275,,MONDO:0020347,acute inflammatory demyelinating polyradiculoneuropathy,
+BMGC_DS16897,BMG_DS065355,,VAN MALDERGEM SYNDROME 1,,,,,DOID:0080585,Van Maldergem syndrome 1,C4551950,,603057;601390,MONDO:0011070,van Maldergem syndrome 1,
+BMGC_DS16898,BMG_DS065356,,,,,,,,,C4551951,,167320,MONDO:0008178,inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1,
+BMGC_DS16899,BMG_DS065357,,"Myopathy, Centronuclear, 1","Myopathies, Structural, Congenital",,,,,,C4551952,D020914,160150;614408,MONDO:0008048,autosomal dominant centronuclear myopathy,
+BMGC_DS16900,BMG_DS065358,,"MACULAR DYSTROPHY, VITELLIFORM, 1",,,,,,,C4551953,,153840,MONDO:0007933,vitelliform macular dystrophy 1,
+BMGC_DS16901,BMG_DS065359,,HYPEREKPLEXIA 1,,,,,,,C4551954,,149400,MONDO:0007868,hyperekplexia 1,
+BMGC_DS16902,BMG_DS065360,,"Loeys-Dietz Syndrome, Type 1a",Loeys-Dietz Syndrome,,,,,,C4551955,D055947,609192,MONDO:0012212,Loeys-Dietz syndrome 1,
+BMGC_DS16903,BMG_DS065361,,,,,,,,,C4551957,,600512,MONDO:0700090,"epilepsy, familial temporal lobe, 1",
+BMGC_DS16904,BMG_DS065362,,"MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1",,,,,DOID:0111185,"myopathy, lactic acidosis, and sideroblastic anemia 1",C4551958,,600462;608109,MONDO:0024553,"myopathy, lactic acidosis, and sideroblastic anemia 1",
+BMGC_DS16905,BMG_DS065363,,ATRIAL STANDSTILL 1,,,,,DOID:0080662,atrial standstill 1,C4551959,,108770,MONDO:0007171,atrial standstill 1,
+BMGC_DS16906,BMG_DS065364,,"Sertoli Cell-Only Syndrome, Type I",,,,,,,C4551960,C537587,400042,MONDO:0010763,"spermatogenic failure, Y-linked, 1",
+BMGC_DS16907,BMG_DS065365,,,,,,,,,C4551961,,,MONDO:0015027,familial isolated hyperparathyroidism,
+BMGC_DS16908,BMG_DS065366,,"ACNE INVERSA, FAMILIAL, 1",,,,,,,C4551962,,142690;605254,MONDO:0007728,"acne inversa, familial, 1",
+BMGC_DS16909,BMG_DS065367,,"GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS 1",,,,,,,C4551964,,607313;608630,MONDO:0020790,"gaze palsy, familial horizontal, with progressive scoliosis 1",
+BMGC_DS16910,BMG_DS065368,,ANAUXETIC DYSPLASIA 1,,,,,DOID:0050640,anauxetic dysplasia 1,C4551965,,157660;607095,MONDO:0054560,anauxetic dysplasia 1,
+BMGC_DS16911,BMG_DS065369,,GLUT1 DEFICIENCY SYNDROME 1,,,,,DOID:0070561,glucose transporter type 1 deficiency syndrome 1,C4551966,,138140;606777,MONDO:0011724,encephalopathy due to GLUT1 deficiency,
+BMGC_DS16912,BMG_DS065370,,B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY,,,,,,,C4551967,,616452;607210,MONDO:0014645,BENTA disease,
+BMGC_DS16913,BMG_DS065371,,"Lissencephaly, X-Linked, 1",Classical Lissencephalies and Subcortical Band Heterotopias,,,,DOID:0060402,chromosome 17p13.1 deletion syndrome,C4551968,D054221,300067,MONDO:0010239,lissencephaly type 1 due to doublecortin gene mutation,
+BMGC_DS16914,BMG_DS065372,,Bilateral Periventricular Nodular Heterotopia,Periventricular Nodular Heterotopia,,,,,,C4551969,D054091,,,,
+BMGC_DS16915,BMG_DS065373,,"Marble Bones, Autosomal Recessive",,,,,,,C4551971,C564915,,,,
+BMGC_DS16916,BMG_DS065374,700056005,Mosaic variegated aneuploidy syndrome,,,,,,,C4551972,,,MONDO:0000141,mosaic variegated aneuploidy syndrome,Mosaic variegated aneuploidy syndrome (disorder) | Mosaic variegated aneuploidy syndrome
+BMGC_DS16917,BMG_DS065375,,Miyoshi Muscular Dystrophy 1,,,,,DOID:0070198,Miyoshi muscular dystrophy,C4551973,C537480,254130,MONDO:0024545,Miyoshi muscular dystrophy 1,
+BMGC_DS16918,BMG_DS065376,,"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 1",,,,,DOID:0070014,autosomal dominant dyskeratosis congenita 1,C4551974,,127550;602322,MONDO:0007485,"dyskeratosis congenita, autosomal dominant 1",
+BMGC_DS16919,BMG_DS065377,,RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 1,,,,,,,C4551975,,605432;142958,MONDO:0024558,radioulnar synostosis with amegakaryocytic thrombocytopenia 1,
+BMGC_DS16920,BMG_DS065378,,HYPOTRICHOSIS 1,,,,,DOID:0110698,hypotrichosis 1,C4551976,,605389;607479,MONDO:0011549,hypotrichosis 1,
+BMGC_DS16921,BMG_DS065380,,HEIMLER SYNDROME 1,,,,,DOID:0080623,Heimler syndrome 1,C4551980,,234580;602136,,,
+BMGC_DS16922,BMG_DS065381,,Familial Multiple Coagulation Factor Deficiency I,,,,,,,C4551981,C565577,227300,MONDO:0009206,"factor V and factor VIII, combined deficiency of, type 1",
+BMGC_DS16923,BMG_DS065382,,TRICHOHEPATOENTERIC SYNDROME 1,,,,,DOID:0111415,trichohepatoenteric syndrome 1,C4551982,,222470;614589,MONDO:0024541,trichohepatoenteric syndrome 1,
+BMGC_DS16924,BMG_DS065383,,"EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 1",,,,,DOID:0081421,familial focal epilepsy with variable foci 1,C4551983,,604364;614191,MONDO:0024556,"epilepsy, familial focal, with variable foci 1",
+BMGC_DS16925,BMG_DS065384,720513002,Arthrogryposis with renal dysfunction and cholestasis syndrome,,,,,,,C4551984,,,MONDO:0017123,arthrogryposis-renal dysfunction-cholestasis syndrome,"Arthrogryposis with renal dysfunction and cholestasis syndrome (disorder) | Arthrogryposis with renal dysfunction and cholestasis syndrome | ARC (arthrogryposis, renal dysfunction, cholestasis) syndrome"
+BMGC_DS16926,BMG_DS065385,,"ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1",,,,,,,C4551985,,173335;208000,MONDO:0008817,"arterial calcification, generalized, of infancy, 1",
+BMGC_DS16927,BMG_DS065386,,AMR Syndrome,,,,,,,C4551986,C565965,,,,
+BMGC_DS16928,BMG_DS065387,,Acrofrontofacionasal Dysostosis 1,,,,,,,C4551987,C538186,201180,MONDO:0100044,acrofrontofacionasal dysostosis 1,
+BMGC_DS16929,BMG_DS065388,,BLEPHAROCHEILODONTIC SYNDROME 1,,,,,DOID:0080345,blepharocheilodontic syndrome 1,C4551988,,119580;192090,MONDO:0054740,blepharocheilodontic syndrome 1,
+BMGC_DS16930,BMG_DS065390,,"Hypobetalipoproteinemia, Familial, 1",,,,,,,C4551990,C566267,615558,MONDO:0014252,familial hypobetalipoproteinemia 1,
+BMGC_DS16931,BMG_DS065391,,ANTERIOR SEGMENT DYSGENESIS 1,,,,,DOID:0080606,anterior segment dysgenesis 1,C4551992,,107250,MONDO:0007138,anterior segment dysgenesis 1,
+BMGC_DS16932,BMG_DS065392,,"Amyotrophic Lateral Sclerosis, Familial",,,,,,,C4551993,C531617,,MONDO:0005144,familial amyotrophic lateral sclerosis,
+BMGC_DS16933,BMG_DS065393,,Mitochondrial DNA Depletion Syndrome 1,,,,,DOID:0080127;DOID:0070331;DOID:0080119,mitochondrial DNA depletion syndrome 8b | mitochondrial DNA depletion syndrome 8a | mitochondrial DNA depletion syndrome 1,C4551995,C536350,603041,MONDO:0011283,mitochondrial DNA depletion syndrome 1,
+BMGC_DS16934,BMG_DS065394,,Auriculocondylar syndrome 1,,,,,,,C4551996,C538270,602483,MONDO:0011234,auriculocondylar syndrome 1,
+BMGC_DS16935,BMG_DS065395,,"Porencephaly, Type 1, Autosomal Dominant",Porencephaly,,,,,,C4551998,D065708,175780;607595,MONDO:0008289,brain small vessel disease 1 with or without ocular anomalies,
+BMGC_DS16936,BMG_DS065396,,"MACULAR DYSTROPHY, PATTERNED, 1",,,,,DOID:0060866,patterned macular dystrophy 1,C4551999,,169150;179605,MONDO:0008210,patterned macular dystrophy 1,
+BMGC_DS16937,BMG_DS065397,,Episodic Kinesigenic Dyskinesia 1,,,,,,,C4552000,C537180,128200,MONDO:0100352,episodic kinesigenic dyskinesia 1,
+BMGC_DS16938,BMG_DS065398,,MEIER-GORLIN SYNDROME 1,,,,,DOID:0080512,Meier-Gorlin syndrome 1,C4552001,,224690;601902,MONDO:0009143,Meier-Gorlin syndrome 1,
+BMGC_DS16939,BMG_DS065399,,WEILL-MARCHESANI SYNDROME 1,,,,,,,C4552002,,277600;608990,MONDO:0010194,Weill-Marchesani syndrome 1,
+BMGC_DS16940,BMG_DS065400,720861000,Ehlers-Danlos syndrome progeroid type,,,,,,,C4552003,,130070,MONDO:0020682,"Ehlers-Danlos syndrome, spondylodysplastic type, 1",Ehlers-Danlos syndrome progeroid type (disorder) | Ehlers-Danlos syndrome progeroid type | Defective biosynthesis of proteodermatan sulfate | Defective biosynthesis of proteodermatan sulphate | Galactosyltransferase I deficiency | Xylosylprotein 4-beta-galactosyltransferase deficiency | B4GALT7-related spondylodysplastic EDS (Ehlers-Danlos syndrome)
+BMGC_DS16941,BMG_DS065401,,Distal Myopathy 1,Distal Myopathies,,,,,,C4552004,D049310,160500,MONDO:0008050,MYH7-related skeletal myopathy,
+BMGC_DS16942,BMG_DS065402,,Gonadotropin deficiency,,,,,,,C4552011,,MTHU037332,,,
+BMGC_DS16943,BMG_DS065404,,CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 1,,,,,,,C4552029,,612199;613129,MONDO:0024564,cerebroretinal microangiopathy with calcifications and cysts 1,
+BMGC_DS16944,BMG_DS065405,,"Ciliary Dyskinesia, Primary, 7, With Or Without Situs Inversus",,,,,,,C4552030,C567504,,,,
+BMGC_DS16945,BMG_DS065406,,Cortical Dysplasia-Focal Epilepsy Syndrome,,,,,DOID:0090130,cortical dysplasia-focal epilepsy syndrome,C4552043,C567657,,,,
+BMGC_DS16946,BMG_DS065407,,ABDOMINAL OBESITY-METABOLIC SYNDROME 1,,,,,,,C4552048,,605552,MONDO:0011565,metabolic syndrome X,
+BMGC_DS16947,BMG_DS065408,,"PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 1",,,,,DOID:0111709,focal nonepidermolytic palmoplantar keratoderma 1,C4552049,,148067;613000,MONDO:0013073,"palmoplantar keratoderma, nonepidermolytic, focal 1",
+BMGC_DS16948,BMG_DS065409,,"Pulmonary Hypertension, Primary, 1",Familial Primary Pulmonary Hypertension,,,,,,C4552070,D065627,178600,MONDO:0024533,"pulmonary hypertension, primary, 1",
+BMGC_DS16949,BMG_DS065410,,Infantile Epileptic-Dyskinetic Encephalopathy,,,,,,,C4552072,C567924,,MONDO:0018226,infantile epileptic-dyskinetic encephalopathy,
+BMGC_DS16950,BMG_DS065411,,PSEUDO-TORCH SYNDROME 1,,,,,DOID:0050656,pseudo-TORCH syndrome 1,C4552078,,251290;602876,MONDO:0020789,pseudo-TORCH syndrome 1,
+BMGC_DS16951,BMG_DS065412,,Premature Ovarian Failure 1,Primary Ovarian Insufficiency,,,,,,C4552079,D016649,311360,MONDO:0010706,premature ovarian failure 1,
+BMGC_DS16952,BMG_DS065413,,"HYPOCALCEMIA, AUTOSOMAL DOMINANT 1, WITH BARTTER SYNDROME",,,,,DOID:0090107,autosomal dominant hypocalcemia 1,C4552089,,601198;601199,,,
+BMGC_DS16953,BMG_DS065414,,"Polyarthritis, Juvenile, Rheumatoid Factor Negative","Arthritis, Juvenile",,,,,,C4552091,D001171,,,,
+BMGC_DS16954,BMG_DS065415,,Dowling-Degos disease 1,,,,,,,C4552092,C562924,179850,MONDO:0024534,Dowling-Degos disease 1,
+BMGC_DS16955,BMG_DS065416,,Nevus Sebaceus of Jadassohn,"Nevus, Sebaceous of Jadassohn",,,,,,C4552097,D054000,163200,MONDO:0008097,linear nevus sebaceous syndrome,
+BMGC_DS16956,BMG_DS065417,,Lynch Syndrome,"Colorectal Neoplasms, Hereditary Nonpolyposis",,,,DOID:3883,Lynch syndrome,C4552100,D003123,,MONDO:0005835,Lynch syndrome,
+BMGC_DS16957,BMG_DS065420,1230015008,Hereditary angioedema with C1Inh (C1 esterase inhibitor) deficiency,,,,,,,C4552294,,106100,MONDO:0033946,hereditary angioedema with C1Inh deficiency,Hereditary angioedema with C1Inh (C1 esterase inhibitor) deficiency | Hereditary angioedema with C1 esterase inhibitor deficiency | Hereditary angioedema with C1 esterase inhibitor deficiency (disorder) | HAE (hereditary angioedema) with C1Inh (C1 esterase inhibitor) deficiency | Hereditary angioneurotic oedema with C1 inhibitor deficiency | Hereditary angioneurotic edema with C1 inhibitor deficiency
+BMGC_DS16958,BMG_DS065423,1187615007,TAFRO syndrome,,,,,,,C4552543,C537372,,MONDO:0018702,Castleman-Kojima disease,"Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) | TAFRO syndrome | TAFRO (thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly) syndrome | Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome"
+BMGC_DS16959,BMG_DS065438,,"Epilepsy, Minor","Epilepsy, Absence",,,,DOID:0070309,absence epilepsy,C4552765,D004832,,,,
+BMGC_DS16960,BMG_DS065441,,Cystic Echinococcosis,Echinococcosis,,,,,,C4553297,D004443,,MONDO:0018408,cystic echinococcosis,
+BMGC_DS16961,BMG_DS065445,,Infantile Obesity,Pediatric Obesity,,,,,,C4553478,D063766,,,,
+BMGC_DS16962,BMG_DS065449,,Absence Seizure Disorder,"Epilepsy, Absence",,,,DOID:0070309,absence epilepsy,C4553705,D004832,,,,
+BMGC_DS16963,BMG_DS065452,766881008,"Carney complex, trismus, pseudocamptodactyly syndrome",,,,,,,C4553889,,,,,"Carney complex, trismus, pseudocamptodactyly syndrome | Carney complex variant | Carney complex, trismus, pseudocamptodactyly syndrome (disorder)"
+BMGC_DS16964,BMG_DS065453,,,,,,,,,C4553954,,,MONDO:0016226,specific language disorder,
+BMGC_DS16965,BMG_DS065454,,Common Peroneal Nerve Entrapment,Peroneal Neuropathies,,,,,,C4554052,D020427,,,,
+BMGC_DS16966,BMG_DS065455,768663003,Leukoencephalopathy with mild cerebellar ataxia and white matter edema,,,,,,,C4554120,,615651,MONDO:0014292,leukoencephalopathy with mild cerebellar ataxia and white matter edema,Leukoencephalopathy with mild cerebellar ataxia and white matter edema | CLCN2-related leukoencephalopathy | Leukoencephalopathy with mild cerebellar ataxia and white matter edema (disorder) | Leukoencephalopathy with ataxia | CLCN2 (chloride voltage-gated channel 2) related leukoencephalopathy | CLCN2-related leucoencephalopathy | Leucoencephalopathy with mild cerebellar ataxia and white matter oedema | CLCN2 (chloride voltage-gated channel 2) related leucoencephalopathy | Leucoencephalopathy with ataxia
+BMGC_DS16967,BMG_DS065498,,"FANCONI ANEMIA, COMPLEMENTATION GROUP S",,,,,DOID:0060979,Fanconi anemia complementation group S,C4554406,,113705;617883,MONDO:0054748,"Fanconi anemia, complementation group S",
+BMGC_DS16968,BMG_DS065499,,"AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 3",,,,,DOID:0080932,primary localized cutaneous amyloidosis 3,C4554421,,617920;604368,MONDO:0054765,"amyloidosis, primary localized cutaneous, 3",
+BMGC_DS16969,BMG_DS065500,1163214006;1163215007,Pressure injury,,,,,DOID:8717,decubitus ulcer,C4554531,,,MONDO:0004646,decubitus ulcer,Pressure injury (morphologic abnormality) | Pressure injury | Pressure injury | Pressure injury (disorder)
+BMGC_DS16970,BMG_DS065501,764849002,Amyloidosis cutis dyschromia,,,,,,,C4554601,,,MONDO:0017906,amyloidosis cutis dyschromia,Amyloidosis cutis dyschromia | Amyloidosis cutis dyschromica | Amyloidosis cutis dyschromia (disorder)
+BMGC_DS16971,BMG_DS065505,,"PROTOPORPHYRIA, ERYTHROPOIETIC, 1",,,,,,,C4692546,,612386;177000,MONDO:0008319,"protoporphyria, erythropoietic, 1",
+BMGC_DS16972,BMG_DS065506,,"TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1",,,,,,,C4692564,,601756;211900,MONDO:0100252,"tumoral calcinosis, hyperphosphatemic, familial, 1",
+BMGC_DS16973,BMG_DS065507,,MANDIBULOFACIAL DYSOSTOSIS WITH IMPAIRED INTELLECTUAL DEVELOPMENT,,,,,,,C4692584,,248400,MONDO:0009559,mandibulofacial dysostosis with mental deficiency,
+BMGC_DS16974,BMG_DS065508,,SHWACHMAN-DIAMOND SYNDROME 1,,,,,,,C4692625,,607444;260400,MONDO:0044204,Shwachman-Diamond syndrome 1,
+BMGC_DS16975,BMG_DS065509,,,,,,,,,C4692652,,301013,MONDO:0049222,"intellectual disability, X-linked 107",
+BMGC_DS16976,BMG_DS065510,,,,,,,,,C4692845,,606798,MONDO:0100532,"blepharospasm, benign essential, susceptibility to",
+BMGC_DS16977,BMG_DS065512,,"SEIZURES, BENIGN FAMILIAL INFANTILE, 6",,,,,DOID:0081119;DOID:0060685,benign familial infantile seizures 6 | autosomal dominant nocturnal frontal lobe epilepsy 4,C4692954,,118502;610353,,,
+BMGC_DS16978,BMG_DS065515,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ibb",,,,,,,C4693133,,613861,MONDO:0800353,"congenital disorder of glycosylation, type Ibb",
+BMGC_DS16979,BMG_DS065517,,"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE",,,,,,,C4693325,,617820,MONDO:0060629,"neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive",
+BMGC_DS16980,BMG_DS065518,,ALKURAYA-KUCINSKAS SYNDROME,,,,,DOID:0111555,Alkuraya-Kucinskas syndrome,C4693347,,611565;617822,MONDO:0060631,Alkuraya-Kucinskas syndrome,
+BMGC_DS16981,BMG_DS065520,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 92,,,,,DOID:0080471,developmental and epileptic encephalopathy 92,C4693362,,600232;617829,MONDO:0020631,developmental and epileptic encephalopathy 92,
+BMGC_DS16982,BMG_DS065521,,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58",,,,,DOID:0080285,developmental and epileptic encephalopathy 58,C4693367,,617830,MONDO:0033367,"developmental and epileptic encephalopathy, 58",
+BMGC_DS16983,BMG_DS065522,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 55, WITH SEIZURES",,,,,DOID:0080227,autosomal dominant intellectual developmental disorder 55,C4693371,,610463;617831,MONDO:0030921,"intellectual disability, autosomal dominant 55, with seizures",
+BMGC_DS16984,BMG_DS065523,,DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES,,,,,DOID:0080473,developmental delay and seizures with or without movement abnormalities,C4693376,,617836;608172,MONDO:0044326,developmental delay and seizures with or without movement abnormalities,
+BMGC_DS16985,BMG_DS065524,,,,,,,,,C4693381,,617839,MONDO:0027694,amyotrophic lateral sclerosis type 23,
+BMGC_DS16986,BMG_DS065525,,,,,,,,,C4693389,,617854,MONDO:0030922,"intellectual disability, autosomal dominant 56",
+BMGC_DS16987,BMG_DS065526,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY",,,,,DOID:0060934,"neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy",C4693390,,617862;610397,MONDO:0060640,"neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy",
+BMGC_DS16988,BMG_DS065527,,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES,,,,,,,C4693391,,617864,MONDO:0060641,neurodevelopmental disorder with or without seizures and gait abnormalities,
+BMGC_DS16989,BMG_DS065528,,"NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES",,,,,,,C4693405,,615951;617865,MONDO:0060642,"neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features",
+BMGC_DS16990,BMG_DS065531,,SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY,,,,,DOID:0080293,short-rib thoracic dysplasia 18 with polydactyly,C4693420,,614068;617866,MONDO:0036483,short-rib thoracic dysplasia 18 with polydactyly,
+BMGC_DS16991,BMG_DS065532,,RETINITIS PIGMENTOSA 81,,,,,DOID:0080292,retinitis pigmentosa 81,C4693443,,614068;617871,MONDO:0036482,retinitis pigmentosa 81,
+BMGC_DS16992,BMG_DS065533,1260133007,Syndromic sensorineural deafness due to combined oxidative phosphorylation defect,,,,,,,C4693450,,617872,MONDO:0054741,combined oxidative phosphorylation deficiency 34,Syndromic sensorineural hearing loss due to COXPD (combined oxidative phosphorylation defect) | Syndromic sensorineural deafness due to combined oxidative phosphorylation defect | Syndromic sensorineural deafness due to combined oxidative phosphorylation defect (disorder) | Syndromic sensorineural deafness due to COXPD (combined oxidative phosphorylation defect)
+BMGC_DS16993,BMG_DS065534,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35,,,,,DOID:0111464,combined oxidative phosphorylation deficiency 35,C4693466,,617840;617873,MONDO:0054742,combined oxidative phosphorylation deficiency 35,
+BMGC_DS16994,BMG_DS065535,,POLYCYSTIC LIVER DISEASE 3 WITH OR WITHOUT KIDNEY CYSTS,,,,,DOID:0060976,polycystic liver disease 3,C4693472,,617874,MONDO:0054743,polycystic liver disease 3 with or without kidney cysts,
+BMGC_DS16995,BMG_DS065536,,POLYCYSTIC LIVER DISEASE 4 WITH OR WITHOUT KIDNEY CYSTS,,,,,DOID:0060977,polycystic liver disease 4,C4693479,,603506;617875,MONDO:0044327,polycystic liver disease 4 with or without kidney cysts,
+BMGC_DS16996,BMG_DS065538,,LEBER CONGENITAL AMAUROSIS WITH EARLY-ONSET DEAFNESS,,,,,DOID:0112240,Leber congenital amaurosis with early-onset deafness,C4693498,,617879,MONDO:0060650,Leber congenital amaurosis with early-onset deafness,
+BMGC_DS16997,BMG_DS065539,,"CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G",,,,,DOID:0080294,Charcot-Marie-Tooth disease dominant intermediate G,C4693509,,617882;162280,MONDO:0036484,"Charcot-Marie-Tooth disease, dominant intermediate G",
+BMGC_DS16998,BMG_DS065540,,,,,,,,,C4693523,,617892,MONDO:0054750,"amyotrophic lateral sclerosis, susceptibility to, 24",
+BMGC_DS16999,BMG_DS065541,,SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY,,,,,DOID:0080295,short-rib thoracic dysplasia 19 with or without polydactyly,C4693524,,617895,MONDO:0033485,short-rib thoracic dysplasia 19 with or without polydactyly,
+BMGC_DS17000,BMG_DS065542,,MULTIPLE SYNOSTOSES SYNDROME 4,,,,,DOID:0081320,multiple synostoses syndrome 4,C4693531,,617898;601147,MONDO:0054752,multiple synostoses syndrome 4,
+BMGC_DS17001,BMG_DS065543,,"LEUKODYSTROPHY, HYPOMYELINATING, 14",,,,,DOID:0080296,hypomyelinating leukodystrophy 14,C4693535,,610553;617899,MONDO:0033486,"leukodystrophy, hypomyelinating, 14",
+BMGC_DS17002,BMG_DS065544,,,,,,,,,C4693542,,617900,MONDO:0054754,"encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8",
+BMGC_DS17003,BMG_DS065545,,NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS,,,,,,,C4693546,,607340;617903,MONDO:0060659,neurodevelopmental disorder with poor language and loss of hand skills,
+BMGC_DS17004,BMG_DS065546,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 59,,,,,DOID:0080291,developmental and epileptic encephalopathy 59,C4693550,,607340;617904,MONDO:0033368,"developmental and epileptic encephalopathy, 59",
+BMGC_DS17005,BMG_DS065547,,"ERYTHROCYTOSIS, FAMILIAL, 5",,,,,DOID:0080290,familial erythrocytosis 5,C4693552,,617907;133170,MONDO:0033483,"erythrocytosis, familial, 5",
+BMGC_DS17006,BMG_DS065548,,DIAMOND-BLACKFAN ANEMIA-LIKE,,,,,,,C4693556,,133170;617911,MONDO:0060662,Diamond-Blackfan anemia-like,
+BMGC_DS17007,BMG_DS065549,,"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5",,,,,,,C4693563,,611496;617912,MONDO:0060663,"congenital heart defects, multiple types, 5",
+BMGC_DS17008,BMG_DS065550,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES",,,,,DOID:0081263,"neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities",C4693567,,617913;606969,MONDO:0060664,"neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities",
+BMGC_DS17009,BMG_DS065551,,,,,,,,,C4693572,,617914,MONDO:0054761,"microcephaly 20, primary, autosomal recessive",
+BMGC_DS17010,BMG_DS065552,,"HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME",,,,,,,C4693578,,602618;617915,MONDO:0060666,"hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome",
+BMGC_DS17011,BMG_DS065553,,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7,,,,,,,C4693583,,614825;617916,MONDO:0054763,neurodegeneration with brain iron accumulation 7,
+BMGC_DS17012,BMG_DS065554,,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8,,,,,,,C4693587,,600184;617917,MONDO:0054764,neurodegeneration with brain iron accumulation 8,
+BMGC_DS17013,BMG_DS065555,,,,,,,,,C4693609,,617921,MONDO:0060670,"amyotrophic lateral sclerosis, susceptibility to, 25",
+BMGC_DS17014,BMG_DS065556,,,,,,,,,C4693613,,617924,MONDO:0060671,"epilepsy, juvenile myoclonic, susceptibility to, 10",
+BMGC_DS17015,BMG_DS065557,,SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY,,,,,,,C4693616,,610621;617925,MONDO:0044328,short-rib thoracic dysplasia 20 with polydactyly,
+BMGC_DS17016,BMG_DS065558,,OROFACIODIGITAL SYNDROME XVII,,,,,DOID:0080289,orofaciodigital syndrome XVII,C4693640,,610621;617926,MONDO:0033375,orofaciodigital syndrome 17,
+BMGC_DS17017,BMG_DS065559,,KERATOCONUS 9,,,,,,,C4693660,,617928;617878,MONDO:0054771,keratoconus 9,
+BMGC_DS17018,BMG_DS065560,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 60,,,,,DOID:0080432,developmental and epileptic encephalopathy 60,C4693663,,610774;617929,MONDO:0033369,"developmental and epileptic encephalopathy, 60",
+BMGC_DS17019,BMG_DS065561,,CHROMOSOME 1p35 DELETION SYNDROME,,,,,,,C4693669,,617930,MONDO:0060677,chromosome 1p35 deletion syndrome,
+BMGC_DS17020,BMG_DS065562,1260097007,"PUM1-associated developmental disability, ataxia, seizure syndrome",,,,,,,C4693672,,617931,MONDO:0033482,spinocerebellar ataxia 47,"PADDAS syndrome | SCA47 - spinocerebellar ataxia type 47 | Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome | Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | PUM1-associated developmental disability, ataxia, seizure syndrome"
+BMGC_DS17021,BMG_DS065563,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 61,,,,,DOID:0080434,developmental and epileptic encephalopathy 61,C4693688,,617933;603709,MONDO:0033370,"developmental and epileptic encephalopathy, 61",
+BMGC_DS17022,BMG_DS065564,,"EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 4",,,,,DOID:0081424,familial focal epilepsy with variable foci 4,C4693694,,182391;617935,MONDO:0054776,"epilepsy, familial focal, with variable foci 4",
+BMGC_DS17023,BMG_DS065565,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 62,,,,,DOID:0080420,developmental and epileptic encephalopathy 62,C4693699,,617938;182391,MONDO:0033371,"developmental and epileptic encephalopathy, 62",
+BMGC_DS17024,BMG_DS065566,,SHWACHMAN-DIAMOND SYNDROME 2,,,,,,,C4693704,,617538;617941,MONDO:0044205,Shwachman-Diamond syndrome 2,
+BMGC_DS17025,BMG_DS065567,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36,,,,,DOID:0111482,combined oxidative phosphorylation deficiency 36,C4693722,,617950;611971,MONDO:0054781,combined oxidative phosphorylation deficiency 36,
+BMGC_DS17026,BMG_DS065568,,"LEUKODYSTROPHY, HYPOMYELINATING, 15",,,,,DOID:0070398,hypomyelinating leukodystrophy 15,C4693733,,138295;617951,MONDO:0054782,"leukodystrophy, hypomyelinating, 15",
+BMGC_DS17027,BMG_DS065569,,"OSTEOGENESIS IMPERFECTA, TYPE XVIII",,,,,DOID:0111848,osteogenesis imperfecta type 18,C4693736,,611357;617952,MONDO:0044329,"osteogenesis imperfecta, type 18",
+BMGC_DS17028,BMG_DS065570,1279891002,Multiple mitochondrial dysfunctions syndrome type 6,,,,,,,C4693741,,617954,MONDO:0054785,multiple mitochondrial dysfunctions syndrome 6,Multiple mitochondrial dysfunctions syndrome type 6 (disorder) | PMPCB (peptidase mitochondrial processing subunit beta) deficiency | PMPCB deficiency | Multiple mitochondrial dysfunctions syndrome type 6
+BMGC_DS17029,BMG_DS065571,,SPERMATOGENIC FAILURE 24,,,,,DOID:0111929,spermatogenic failure 24,C4693751,,617949;617959,MONDO:0054728,spermatogenic failure 24,
+BMGC_DS17030,BMG_DS065572,,SPERMATOGENIC FAILURE 25,,,,,DOID:0111920,spermatogenic failure 25,C4693765,,617960;605795,MONDO:0054729,spermatogenic failure 25,
+BMGC_DS17031,BMG_DS065574,,SPERMATOGENIC FAILURE 26,,,,,DOID:0111924,spermatogenic failure 26,C4693773,,617961;607166,MONDO:0054730,spermatogenic failure 26,
+BMGC_DS17032,BMG_DS065575,,"LEUKODYSTROPHY, HYPOMYELINATING, 16",,,,,DOID:0070405,hypomyelinating leukodystrophy 16,C4693779,,613413;617964,MONDO:0054791,"leukodystrophy, hypomyelinating, 16",
+BMGC_DS17033,BMG_DS065576,,SPERMATOGENIC FAILURE 27,,,,,DOID:0111928,spermatogenic failure 27,C4693784,,615364;617965,MONDO:0054731,spermatogenic failure 27,
+BMGC_DS17034,BMG_DS065577,,"RH-NULL, AMORPH TYPE",,,,,,,C4693796,,111700;617970,,,
+BMGC_DS17035,BMG_DS065578,,"METHEMOGLOBINEMIA, ALPHA TYPE",,,,,,,C4693798,,617973,MONDO:0020835,"methemoglobinemia, alpha type",
+BMGC_DS17036,BMG_DS065579,,"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, DI ROCCO TYPE",,,,,,,C4693799,,611482;617974,MONDO:0060702,"spondyloepimetaphyseal dysplasia, di rocco type",
+BMGC_DS17037,BMG_DS065580,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 63,,,,,DOID:0080426,developmental and epileptic encephalopathy 63,C4693810,,617976;605032,MONDO:0033372,"developmental and epileptic encephalopathy, 63",
+BMGC_DS17038,BMG_DS065581,,NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES,,,,,,,C4693816,,609226;617977,MONDO:0060704,neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures,
+BMGC_DS17039,BMG_DS065582,,"ERYTHROCYTOSIS, FAMILIAL, 6",,,,,DOID:0111632,familial erythrocytosis 6,C4693822,,617980,MONDO:0054801,"erythrocytosis, familial, 6",
+BMGC_DS17040,BMG_DS065583,,"ERYTHROCYTOSIS, FAMILIAL, 7",,,,,DOID:0111631,familial erythrocytosis 7,C4693823,,617981,MONDO:0054802,"erythrocytosis, familial, 7",
+BMGC_DS17041,BMG_DS065584,,VERVERI-BRADY SYNDROME,,,,,,,C4693824,,617982;617387,MONDO:0060707,Ververi-Brady syndrome,
+BMGC_DS17042,BMG_DS065585,,"MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE",,,,,,,C4693831,,617983;615638,MONDO:0054804,"microcephaly 21, primary, autosomal recessive",
+BMGC_DS17043,BMG_DS065586,,"MICROCEPHALY 22, PRIMARY, AUTOSOMAL RECESSIVE",,,,,,,C4693834,,617984;609276,MONDO:0054805,"microcephaly 22, primary, autosomal recessive",
+BMGC_DS17044,BMG_DS065587,,"MICROCEPHALY 23, PRIMARY, AUTOSOMAL RECESSIVE",,,,,,,C4693843,,602332;617985,MONDO:0054806,"microcephaly 23, primary, autosomal recessive",
+BMGC_DS17045,BMG_DS065588,,JABERI-ELAHI SYNDROME,,,,,,,C4693848,,607434;617988,MONDO:0060711,Jaberi-Elahi syndrome,
+BMGC_DS17046,BMG_DS065589,1208987006,"PHIP-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome",,,,,,,C4693860,,617991,MONDO:0035133,PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome,"PHIP-related behavioural problems, intellectual disability, obesity, dysmorphic features syndrome | PHIP-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Pleckstrin homology domain interacting protein-related behavioural problems, intellectual disability, obesity, dysmorphic features syndrome | Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome (disorder) | Chung Jansen syndrome"
+BMGC_DS17047,BMG_DS065590,,"TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2",,,,,,,C4693863,,617993,MONDO:0060714,"tumoral calcinosis, hyperphosphatemic, familial, 2",
+BMGC_DS17048,BMG_DS065591,,"TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 3",,,,,,,C4693864,,617994,MONDO:0060715,"tumoral calcinosis, hyperphosphatemic, familial, 3",
+BMGC_DS17049,BMG_DS065592,,,,,,,,,C4693865,,617996,MONDO:0020837,oocyte maturation defect 5,
+BMGC_DS17050,BMG_DS065593,1255121003,Classical-like Ehlers-Danlos syndrome type 2,,,,,,,C4693870,,618000,MONDO:0054813,"Ehlers-Danlos syndrome, classic-like, 2",Classical-like Ehlers-Danlos syndrome type 2 | AEBP1-related Ehlers-Danlos syndrome | Classical-like Ehlers-Danlos syndrome type 2 (disorder) | AEBP1-related EDS (Ehlers-Danlos syndrome)
+BMGC_DS17051,BMG_DS065594,,"DEAFNESS, AUTOSOMAL RECESSIVE 57",,,,,DOID:0111635,autosomal recessive nonsyndromic deafness 57,C4693893,,612971;618003,MONDO:0033201,"hearing loss, autosomal recessive 57",
+BMGC_DS17052,BMG_DS065595,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 64,,,,,DOID:0070375,developmental and epileptic encephalopathy 64,C4693899,,607352;618004,MONDO:0033373,"developmental and epileptic encephalopathy, 64",
+BMGC_DS17053,BMG_DS065596,,CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION 1,,,,,,,C4693905,,618005;602589,MONDO:0060720,congenital disorder of glycosylation with defective fucosylation,
+BMGC_DS17054,BMG_DS065597,,"LEUKODYSTROPHY, HYPOMYELINATING, 17",,,,,DOID:0070404,hypomyelinating leukodystrophy 17,C4693912,,618006;600859,MONDO:0054817,"leukodystrophy, hypomyelinating, 17",
+BMGC_DS17055,BMG_DS065598,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 65,,,,,DOID:0080430,developmental and epileptic encephalopathy 65,C4693925,,606323;618008,MONDO:0033374,"developmental and epileptic encephalopathy, 65",
+BMGC_DS17056,BMG_DS065599,,HYPEREKPLEXIA 4,,,,,DOID:0080581,hyperekplexia 4,C4693933,,614452;618011,MONDO:0044330,hyperekplexia 4,
+BMGC_DS17057,BMG_DS065600,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 93,,,,,DOID:0112275,developmental and epileptic encephalopathy 93,C4693934,,607027;618012,MONDO:0020632,developmental and epileptic encephalopathy 93,
+BMGC_DS17058,BMG_DS065601,,"DEAFNESS, AUTOSOMAL RECESSIVE 109",,,,,DOID:0111639,autosomal recessive nonsyndromic deafness 109,C4693935,,612959;618013,MONDO:0033202,"hearing loss, autosomal recessive 109",
+BMGC_DS17059,BMG_DS065602,,PREMATURE OVARIAN FAILURE 14,,,,,DOID:0080871,primary ovarian insufficiency 14,C4693941,,618014;601918,MONDO:0044777,premature ovarian failure 14,
+BMGC_DS17060,BMG_DS065603,,"PROTOPORPHYRIA, ERYTHROPOIETIC, 2",,,,,,,C4693947,,618015;615611,MONDO:0060729,"protoporphyria, erythropoietic, 2",
+BMGC_DS17061,BMG_DS065604,,"DRUG METABOLISM, ALTERED, CYP2C8-RELATED",,,,,,,C4693948,,601129;618018,,,
+BMGC_DS17062,BMG_DS065616,,"METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC",,,,,DOID:0050715,methylmalonic aciduria and homocystinuria type cblC,C4693974,,176763;609831;277400,,,
+BMGC_DS17063,BMG_DS065639,,"HEMOGLOBIN M (RADOM) METHEMOGLOBINEMIA, BETA TYPE",,,,,,,C4694049,,141900,,,
+BMGC_DS17064,BMG_DS065640,,POLYCYSTIC OVARY SYNDROME DUE TO 17-KETOSTEROID REDUCTASE DEFICIENCY,,,,,DOID:0112248,17-beta hydroxysteroid dehydrogenase 3 deficiency,C4694050,,264300,,,
+BMGC_DS17065,BMG_DS065642,,,,,,,,,C4700504,,,MONDO:0005500,congenital disorder of glycosylation type I,
+BMGC_DS17066,BMG_DS065657,,,,,,,,,C4703420,,600251,MONDO:0010850,Tessier number 4 facial cleft,
+BMGC_DS17067,BMG_DS065658,,Severe Cytomegalovirus Infection,Cytomegalovirus Infections,,,,,,C4703481,D003586,,,,
+BMGC_DS17068,BMG_DS065665,,Stationary Cone Dystrophy,Cone Dystrophy,,,,DOID:0050795,cone dystrophy,C4704791,D000077765,,,,
+BMGC_DS17069,BMG_DS065666,,"Polyarthritis, Juvenile, Rheumatoid Factor Positive","Arthritis, Juvenile",,,,,,C4704862,D001171,,,,
+BMGC_DS17070,BMG_DS065667,,Genital Vulvovaginal Candidiasis,"Candidiasis, Vulvovaginal",,,,,,C4704876,D002181,,,,
+BMGC_DS17071,BMG_DS065668,,Fibrocystic Dysplasia of Bone,Fibrous Dysplasia of Bone,,,,,,C4704884,D005357,,,,
+BMGC_DS17072,BMG_DS065669,,Fibrocartilaginous Dysplasia of Bone,Fibrous Dysplasia of Bone,,,,,,C4704885,D005357,,,,
+BMGC_DS17073,BMG_DS065670,,Maternal Sepsis,"Pregnancy Complications, Infectious",,,,,,C4704910,D011251,,,,
+BMGC_DS17074,BMG_DS065671,,Posterior Interosseous Nerve Syndrome,Radial Neuropathy,,,,,,C4704934,D020425,,,,
+BMGC_DS17075,BMG_DS065672,,Femoral Nerve Dysfunction,Femoral Neuropathy,,,,,,C4704935,D020428,,,,
+BMGC_DS17076,BMG_DS065675,763062006,2q33.1 microdeletion syndrome,,,,,,,C4706258,,,MONDO:0016653,2q33.1 microdeletion syndrome,2q33.1 microdeletion syndrome (disorder) | 2q33.1 microdeletion syndrome | Monosomy 2q33.1
+BMGC_DS17077,BMG_DS065678,763110007,Combined oxidative phosphorylation defect type 13,,,,,,,C4706283,,614932,MONDO:0013977,combined oxidative phosphorylation defect type 13,Combined oxidative phosphorylation defect type 13 (disorder) | Combined oxidative phosphorylation defect type 13 | COXPD13 - combined oxidative phosphorylation defect type 13
+BMGC_DS17078,BMG_DS065683,763203009,Combined oxidative phosphorylation defect type 15,,,,,,,C4706313,,614947,MONDO:0013987,combined oxidative phosphorylation defect type 15,COXPD15 - combined oxidative phosphorylation defect type 15 | Combined oxidative phosphorylation defect type 15 (disorder) | Combined oxidative phosphorylation defect type 15
+BMGC_DS17079,BMG_DS065684,763209008,Combined oxidative phosphorylation defect type 9,,,,,,,C4706315,,614582,MONDO:0013811,combined oxidative phosphorylation defect type 9,Combined oxidative phosphorylation defect type 9 (disorder) | Combined oxidative phosphorylation defect type 9 | COXPD9 - combined oxidative phosphorylation defect type 9
+BMGC_DS17080,BMG_DS065685,763211004,Combined oxidative phosphorylation defect type 21,,,,,,,C4706316,,615918,MONDO:0014398,combined oxidative phosphorylation defect type 21,COXPD21 - combined oxidative phosphorylation defect type 21 | Combined oxidative phosphorylation defect type 21 | Combined oxidative phosphorylation defect type 21 (disorder)
+BMGC_DS17081,BMG_DS065695,763280005,"Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome",,,,,,,C4706367,,,,,"Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome (disorder)"
+BMGC_DS17082,BMG_DS065696,,,,,,,,,C4706386,,,MONDO:0018437,acute myeloid leukemia with NPM1 somatic mutations,
+BMGC_DS17083,BMG_DS065700,763315005,Congenital myopathy with myasthenic-like onset,,,,,,,C4706390,,,MONDO:0018528,congenital myopathy with myasthenic-like onset,Congenital myopathy with myasthenic-like onset (disorder) | Congenital myopathy with myasthenic-like onset
+BMGC_DS17084,BMG_DS065703,763318007,Connective tissue disorder due to lysyl hydroxylase-3 deficiency,,,,,,,C4706393,,,,,"Bone fragillity, contractures, arterial rupture, deafness syndrome | Connective tissue disorder due to lysyl hydroxylase-3 deficiency | Bone fragility, contractures, arterial rupture, deafness syndrome | Connective tissue disorder due to lysyl hydroxylase-3 deficiency (disorder) | Connective tissue disorder due to LH3 deficiency"
+BMGC_DS17085,BMG_DS065704,763346009,Lethal congenital contracture syndrome type 5,,,,,,,C4706410,,615368,MONDO:0014149,fetal akinesia-cerebral and retinal hemorrhage syndrome,"Fetal akinesia, cerebral and retinal haemorrhage syndrome | Lethal congenital contracture syndrome type 5 | Fetal akinesia, cerebral and retinal hemorrhage syndrome (disorder) | Fetal akinesia, cerebral and retinal hemorrhage syndrome | Foetal akinesia, cerebral and retinal haemorrhage syndrome"
+BMGC_DS17086,BMG_DS065705,763348005,Autosomal recessive cerebellar ataxia with late-onset spasticity,,,,,,,C4706412,,,MONDO:0018129,autosomal recessive cerebellar ataxia with late-onset spasticity,Autosomal recessive cerebellar ataxia due to GBA2 (glucosylceramidase beta 2) deficiency | Autosomal recessive cerebellar ataxia with late-onset spasticity | Autosomal recessive cerebellar ataxia with late-onset spasticity (disorder)
+BMGC_DS17087,BMG_DS065706,763349002,Progressive myoclonic epilepsy with dystonia,,,,,,,C4706413,,,MONDO:0018126,progressive myoclonic epilepsy with dystonia,Progressive myoclonus epilepsy with dystonia | Progressive myoclonic epilepsy with dystonia | Progressive myoclonic epilepsy with dystonia (disorder)
+BMGC_DS17088,BMG_DS065707,763350002,"Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome",,,,,,,C4706414,,,MONDO:0018123,intellectual disability-obesity-brain malformations-facial dysmorphism syndrome,"Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome | Autosomal recessive intellectual disability due to TRAPPC9 (trafficking protein particle complex 9) deficiency | Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome (disorder)"
+BMGC_DS17089,BMG_DS065708,763351003,Spectrin-associated autosomal recessive cerebellar ataxia,,,,,,,C4706415,,615386,MONDO:0014159,autosomal recessive spinocerebellar ataxia 14,"Spectrin-associated autosomal recessive cerebellar ataxia | Autosomal recessive spinocerebellar ataxia type 14 | Autosomal recessive cerebellar ataxia, cognitive defect syndrome | Spectrin-associated autosomal recessive cerebellar ataxia (disorder) | Spectrin-associated autosomal recessive cerebellar ataxia type 1"
+BMGC_DS17090,BMG_DS065709,763366000,"Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome",,,,,,,C4706421,,614924,MONDO:0013971,leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome,"Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome (disorder) | COXPD12 - combined oxidative phosphorylation defect type 12 | Combined oxidative phosphorylation defect type 12 | Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome"
+BMGC_DS17091,BMG_DS065710,763368004,Familial progressive hyperpigmentation and hypopigmentation of skin,,,,,,,C4706423,,,MONDO:0017239,familial progressive hyper- and hypopigmentation,Familial progressive hyperpigmentation and hypopigmentation of skin | Familial progressive hyper and hypopigmentation | Familial progressive hyperpigmentation and hypopigmentation of skin (disorder)
+BMGC_DS17092,BMG_DS065719,763528002,Distal monosomy 3p syndrome,,,,,,,C4706503,,613792,MONDO:0013424,3p- syndrome,Distal monosomy 3p syndrome | Distal 3p deletion | Distal monosomy 3p | Distal monosomy 3p syndrome (disorder) | 3p syndrome
+BMGC_DS17093,BMG_DS065722,763534009,Hot water reflex epilepsy,,,,,,,C4706506,,,MONDO:0013229,hot water reflex epilepsy,Hot water reflex epilepsy | Hot water reflex epilepsy (disorder)
+BMGC_DS17094,BMG_DS065728,763623001,Severe combined immunodeficiency due to CTPS1 deficiency,,,,,,,C4706524,,,,,Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency | Severe combined immunodeficiency due to CTPS1 deficiency | Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency (disorder)
+BMGC_DS17095,BMG_DS065732,763688008,"Deafness, encephaloneuropathy, obesity, valvulopathy syndrome",,,,,,,C4706538,,,,,"Hearing loss, encephaloneuropathy, obesity, valvulopathy syndrome | Deafness, encephaloneuropathy, obesity, valvulopathy syndrome | Deafness, encephaloneuropathy, obesity, valvulopathy syndrome (disorder)"
+BMGC_DS17096,BMG_DS065733,763713000,Idiopathic CD4 lymphocytopenia,,,,,,,C4706550,,,,,Idiopathic CD4 lymphocytopenia (disorder) | Idiopathic CD4 lymphocytopenia | ICL - idiopathic CD4 lymphocytopenia
+BMGC_DS17097,BMG_DS065734,763715007,Familial hyperprolactinemia,,,,,,,C4706551,,615555,MONDO:0014250,familial hyperprolactinemia,Familial hyperprolactinemia | Familial hyperprolactinemia (disorder) | Familial hyperprolactinaemia | Familial isolated prolactin receptor deficiency
+BMGC_DS17098,BMG_DS065735,,,,,,,,,C4706552,,,MONDO:0017329,familial vesicoureteral reflux,
+BMGC_DS17099,BMG_DS065737,763721006,Hypermethioninemia encephalopathy due to deficiency of adenosine kinase,,,,,,,C4706555,,611094;614300,MONDO:0100255,adenosine kinase deficiency,Hypermethioninemia encephalopathy due to deficiency of adenosine kinase (disorder) | Hypermethioninemia encephalopathy due to deficiency of adenosine kinase | Hypermethioninaemia encephalopathy due to deficiency of adenosine kinase | Hypermethioninemia encephalopathy due to ADK (adenosine kinase) deficiency | Hypermethioninaemia encephalopathy due to ADK (adenosine kinase) deficiency
+BMGC_DS17100,BMG_DS065738,763722004,"Hypotonia, speech impairment, severe cognitive delay syndrome",,,,,,,C4706556,,,MONDO:0014176,"hypotonia, infantile, with psychomotor retardation and characteristic facies","Hypotonia, speech impairment, severe cognitive delay syndrome (disorder) | Hypotonia, speech impairment, severe cognitive delay syndrome | IHPRF (infantile hypotonia, psychomotor retardation, characteristic facies) syndrome"
+BMGC_DS17101,BMG_DS065740,763741001,"Intellectual disability, alacrima, achalasia syndrome",,,,,,,C4706563,,615510,MONDO:0014219,"alacrima, achalasia, and intellectual disability syndrome","Intellectual disability, alacrima, achalasia syndrome (disorder) | Intellectual disability, alacrima, achalasia syndrome"
+BMGC_DS17102,BMG_DS065744,763773007,Macrocephaly and developmental delay syndrome,,,,,,,C4706573,,,,,Macrocephaly and developmental delay syndrome | Macrocephaly and developmental delay syndrome (disorder)
+BMGC_DS17103,BMG_DS065745,763776004,KLHL9-related early-onset distal myopathy,,,,,,,C4706574,,,MONDO:0018370,KLHL9-related early-onset distal myopathy,KLHL9-related early-onset distal myopathy | Kelch like family member 9 related early-onset distal myopathy (disorder) | Kelch like family member 9 related early-onset distal myopathy
+BMGC_DS17104,BMG_DS065746,763778003,Larsen-like syndrome B3GAT3 type,,,,,,,C4706575,,,,,"Larsen-like syndrome beta-1,3-glucuronyltransferase 3 type | Multiple joint dislocations, short stature, craniofacial dysmorphism, congenital heart defects syndrome | Larsen-like syndrome B3GAT3 type | Larsen-like syndrome beta-1,3-glucuronyltransferase 3 type (disorder)"
+BMGC_DS17105,BMG_DS065749,,,,,,,,,C4706584,,,MONDO:0018436,megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13),
+BMGC_DS17106,BMG_DS065750,763798008,"Microcephalus, complex motor and sensory axonal neuropathy syndrome",,,,,,,C4706585,,,MONDO:0018507,microcephaly-complex motor and sensory axonal neuropathy syndrome,"Microcephalus, complex motor and sensory axonal neuropathy syndrome | Microcephaly, complex motor and sensory axonal neuropathy syndrome | Microcephalus, complex motor and sensory axonal neuropathy syndrome (disorder)"
+BMGC_DS17107,BMG_DS065752,763815000,Oculoauricular syndrome Schorderet type,,,,,,,C4706592,,,,,Oculoauricular syndrome Schorderet type | Oculoauricular syndrome Schorderet type (disorder)
+BMGC_DS17108,BMG_DS065757,763837007,Oro-facial digital syndrome type 14,,,,,,,C4706604,,615948,MONDO:0014413,orofaciodigital syndrome type 14,"Oro-facial digital syndrome type 14 | Oro-facial digital syndrome type 14 (disorder) | Microcephaly, cerebral malformation, orofaciodigital syndrome | Orofaciodigital syndrome type 14"
+BMGC_DS17109,BMG_DS065760,763868006,SHOX-related short stature,,,,,,,C4706613,,,,,SHOX-related short stature | Short stature homeobox related short stature (disorder) | Short stature homeobox related short stature | SHOX (short stature homeobox) related short stature
+BMGC_DS17110,BMG_DS065782,763886009,Spondyloperipheral dysplasia with short ulna syndrome,,,,,,,C4706658,,,,,Spondyloperipheral dysplasia with short ulna syndrome (disorder) | Spondyloperipheral dysplasia with short ulna syndrome
+BMGC_DS17111,BMG_DS065785,763890006,Short stature with delayed bone age due to thyroid hormone metabolism deficiency,,,,,,,C4706661,,,,,Short stature with delayed bone age due to thyroid hormone metabolism deficiency (disorder) | Short stature with delayed bone age due to thyroid hormone metabolism deficiency
+BMGC_DS17112,BMG_DS065786,764095005,"Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome",,,,,,,C4706676,,,,,"Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome (disorder) | Ataxia, delayed dentition, hypomyelination syndrome | Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome"
+BMGC_DS17113,BMG_DS065787,764096006,Male infertility with teratozoospermia due to single gene mutation,,,,,,,C4706677,,,MONDO:0018394,male infertility with teratozoospermia due to single gene mutation,Male infertility with teratozoospermia due to single gene mutation (disorder) | Male infertility with teratozoospermia due to single gene mutation
+BMGC_DS17114,BMG_DS065795,764108000,Wooly hair with palmoplantar keratoderma syndrome,,,,,DOID:0070554,palmoplantar keratoderma and woolly hair,C4706686,,,,,Wooly hair with palmoplantar keratoderma syndrome | Woolly hair with palmoplantar keratoderma syndrome | Wooly hair with palmoplantar keratoderma syndrome (disorder) | Keratoderma with woolly hair type IV | Keratoderma with wooly hair type IV
+BMGC_DS17115,BMG_DS065826,764456001,Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency,,,,,,,C4706871,,,,,CA-VA (carbonic anhydrase VA) deficiency | Carbonic anhydrase VA deficiency | Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency (disorder) | Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency | CA5A related hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency | Carbonic anhydrase 5A related hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
+BMGC_DS17116,BMG_DS065837,,,,,,,,,C4706941,,,MONDO:0018472,familial isolated trichomegaly,
+BMGC_DS17117,BMG_DS065845,764696007,Distal 17p13.3 microdeletion syndrome,,,,,,,C4707092,,,MONDO:0016839,distal 17p13.3 microdeletion syndrome,Distal 17p13.3 microdeletion syndrome | Distal monosomy 17p13.3 | Distal 17p13.3 microdeletion syndrome (disorder)
+BMGC_DS17118,BMG_DS065849,764733009,"Progressive external ophthalmoplegia, myopathy, emaciation syndrome",,,,,,,C4707098,,,,,"Progressive external ophthalmoplegia, myopathy, emaciation syndrome | Progressive external ophthalmoplegia, myopathy, emaciation syndrome (disorder) | PEO (progressive external ophthalmoplegia) myopathy emaciation syndrome | Mitochondrial DNA (deoxyribonucleic acid) maintenance syndrome due to MGME1 (mitochondrial genome maintenance exonuclease 1) deficiency"
+BMGC_DS17119,BMG_DS065853,764812008,Autosomal recessive myogenic arthrogryposis multiplex congenita,,,,,,,C4707155,,,MONDO:0017892,autosomal recessive myogenic arthrogryposis multiplex congenita,Autosomal recessive myogenic arthrogryposis multiplex congenita (disorder) | Autosomal recessive myogenic arthrogryposis multiplex congenita | SYNE1-related arthrogryposis multiplex congenita | SYNE1 (spectrin repeat containing nuclear envelope protein 1) related arthrogryposis multiplex congenita
+BMGC_DS17120,BMG_DS065854,764730007,Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation,,,,,,,C4707173,,,MONDO:0017940,autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation,Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation (disorder) | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
+BMGC_DS17121,BMG_DS065855,,,,,,,,,C4707178,,,MONDO:0017894,acute myeloid leukemia with CEBPA somatic mutations,
+BMGC_DS17122,BMG_DS065857,764857004,"Tibial hemimelia, polysyndactyly, triphalangeal thumb syndrome",,,,,,,C4707180,,,,,"Absent tibia polydactyly syndrome | Tibial hemimelia, polysyndactyly, triphalangeal thumb syndrome | Tibial hemimelia, polysyndactyly, triphalangeal thumb syndrome (disorder)"
+BMGC_DS17123,BMG_DS065859,,,,,,,,,C4707228,,,MONDO:0017893,inherited acute myeloid leukemia,
+BMGC_DS17124,BMG_DS065860,764942005,"Colobomatous microphthalmia, rhizomelic dysplasia syndrome",,,,,,,C4707229,,,,,"Colobomatous microphthalmia, rhizomelic dysplasia syndrome (disorder) | Colobomatous microphthalmia, rhizomelic dysplasia syndrome | Microphthalmia, coloboma, rhizomelic skeletal dysplasia"
+BMGC_DS17125,BMG_DS065861,764945007,Congenital myopathy with internal nuclei and atypical cores,,,,,,,C4707232,,614807,MONDO:0013890,congenital myopathy with internal nuclei and atypical cores,Centronuclear myopathy type 4 | Congenital myopathy with internal nuclei and atypical cores (disorder) | Congenital myopathy with internal nuclei and atypical cores
+BMGC_DS17126,BMG_DS065865,764958008,Striate palmoplantar keratoderma,,,,,,,C4707237,,,MONDO:0018865,striate palmoplantar keratoderma,Striate palmoplantar keratoderma (disorder) | Keratosis palmoplantaris varians of Wachters | Keratosis palmoplantaris striata et areata | Striate palmoplantar keratoderma | Keratosis palmoplantaris striata
+BMGC_DS17127,BMG_DS065866,764960005,Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency,,,,,,,C4707238,,,MONDO:0017337,inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency,Inherited isolated adrenal insufficiency due to partial cytochrome P450 family 11 subfamily A member 1 deficiency | Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency | Inherited isolated adrenal insufficiency due to partial cytochrome P450 family 11 subfamily A member 1 deficiency (disorder)
+BMGC_DS17128,BMG_DS065867,764962002,Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1,,,,,,,C4707239,,,,,Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder) | Hepatoencephalopathy due to COXPD1 (combined oxidative phosphorylation defect type 1) | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
+BMGC_DS17129,BMG_DS065869,764965000,Familial thoracic aortic aneurysm and aortic dissection,,,,,,,C4707243,,,MONDO:0019625,familial thoracic aortic aneurysm and aortic dissection,Familial TAAD (thoracic aortic aneurysm aortic dissection) | Familial thoracic aortic aneurysm and aortic dissection | Familial thoracic aortic aneurysm and aortic dissection (disorder)
+BMGC_DS17130,BMG_DS065872,764992006,Muscle filaminopathy,,,,,,,C4707258,,,,,Muscle filaminopathy | Muscle filaminopathy (disorder)
+BMGC_DS17131,BMG_DS065878,765089003,"Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome",,,,,,,C4707306,,,MONDO:0018125,focal epilepsy-intellectual disability-cerebro-cerebellar malformation,"Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (disorder) | Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Focal epilepsy, intellectual disability, dysarthria, ataxia syndrome"
+BMGC_DS17132,BMG_DS065879,765093009,"Rolandic epilepsy, speech dyspraxia syndrome",,,,,,,C4707308,,,MONDO:0015587,rolandic epilepsy-speech dyspraxia syndrome,"Rolandic epilepsy, speech dyspraxia syndrome (disorder) | Rolandic epilepsy, speech dyspraxia syndrome"
+BMGC_DS17133,BMG_DS065881,765137006,Methylmalonic acidemia due to methylmalonyl-coenzyme A epimerase deficiency,,,,,,,C4707328,,,,,Methylmalonic acidemia due to methylmalonyl-CoA racemase deficiency | Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency | Methylmalonic acidaemia due to methylmalonyl-CoA epimerase deficiency | Methylmalonic acidemia due to methylmalonyl-coenzyme A epimerase deficiency (disorder) | Methylmalonic acidaemia due to methylmalonyl-CoA racemase deficiency | Methylmalonic acidemia due to methylmalonyl-coenzyme A epimerase deficiency | Methylmalonic acidaemia due to methylmalonyl-coenzyme A epimerase deficiency | MCEE-gene related methylmalonic acidaemia due to methylmalonyl-coenzyme A epimerase deficiency | MCEE-gene related methylmalonic acidemia due to methylmalonyl-coenzyme A epimerase deficiency
+BMGC_DS17134,BMG_DS065886,,,,,,,,,C4707333,,,MONDO:0017190,sporadic pheochromocytoma/secreting paraganglioma,
+BMGC_DS17135,BMG_DS065887,765145001,T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency,,,,,,,C4707334,,,,,SCIDX1 - severe combined immunodeficiency X-linked | T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency | T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency (disorder) | T-B+ severe combined immunodeficiency due to gamma chain deficiency
+BMGC_DS17136,BMG_DS065890,765188009,Severe combined immunodeficiency due to complete RAG1 and/or RAG2 deficiency,,,,,,,C4707355,,,,,Severe combined immunodeficiency due to complete RAG1 (recombination activating gene 1) and/or RAG2 (recombination activating gene 2) deficiency | SCID (severe combined immunodeficiency) due to complete RAG1/2 deficiency | Severe combined immunodeficiency due to complete RAG1 and/or RAG2 deficiency | Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency | Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency (disorder)
+BMGC_DS17137,BMG_DS065892,765195000,Familial generalized lentiginosis,,,,,,,C4707357,,,,,Familial generalised lentiginosis | Familial generalized lentiginosis (disorder) | Familial generalized lentiginosis | Familial multiple lentigines syndrome without systemic involvement | Familial lentigines profusa
+BMGC_DS17138,BMG_DS065893,765196004,Distal myotilinopathy,,,,,,,C4707358,,,,,Distal myotilinopathy | Distal myotilinopathy (disorder)
+BMGC_DS17139,BMG_DS065894,765197008,Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier,,,,,,,C4707359,,,MONDO:0016097,symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers,Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier | Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier (disorder)
+BMGC_DS17140,BMG_DS065895,,,,,,,,,C4707361,,,MONDO:0016995,familial multiple meningioma,
+BMGC_DS17141,BMG_DS065909,765327005,"Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome",,,,,,,C4707403,,,,,"Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome | Congenital sideroblastic anaemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome | Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome (disorder)"
+BMGC_DS17142,BMG_DS065929,766044005,Acute encephalopathy with biphasic seizures and late reduced diffusion,,,,,,,C4707658,,,MONDO:0018198,acute encephalopathy with biphasic seizures and late reduced diffusion,Acute encephalopathy with biphasic seizures and late reduced diffusion | Acute infantile encephalopathy predominantly affecting frontal lobe | Acute encephalopathy with biphasic seizures and late reduced diffusion (disorder)
+BMGC_DS17143,BMG_DS065933,766050000,Distal monosomy 15q,,,,,,,C4707662,,,,,Distal 15q deletion syndrome | Monosomy 15q26 | Distal monosomy 15q | 15q26 deletion syndrome | Telomeric 15q deletion syndrome | Distal monosomy 15q syndrome | Distal monosomy 15q syndrome (disorder)
+BMGC_DS17144,BMG_DS065953,766717008,Multiple epiphyseal dysplasia due to collagen 9 anomaly,,,,,,,C4707798,,,MONDO:0015627,multiple epiphyseal dysplasia due to collagen 9 anomaly,Multiple epiphyseal dysplasia due to collagen 9 anomaly | Multiple epiphyseal dysplasia due to collagen 9 anomaly (disorder)
+BMGC_DS17145,BMG_DS065962,766766005,1p31p32 microdeletion syndrome,,,,,,,C4707828,,,MONDO:0013396,chromosome 1p32-p31 deletion syndrome,1p31p32 microdeletion syndrome | Monosomy 1p31p32 | 1p31p32 microdeletion syndrome (disorder)
+BMGC_DS17146,BMG_DS065963,766767001,Autosomal recessive spastic paraplegia type 67,,,,,,,C4707829,,,MONDO:0018419,autosomal recessive spastic paraplegia type 67,Autosomal recessive spastic paraplegia type 67 (disorder) | Autosomal recessive spastic paraplegia type 67
+BMGC_DS17147,BMG_DS065968,766817004,Short stature due to growth hormone secretagogue receptor deficiency,,,,,,,C4707848,,,,,Short stature due to GHSR (growth hormone secretagogue receptor) deficiency | Short stature due to growth hormone secretagogue receptor deficiency | Short stature due to growth hormone secretagogue receptor deficiency (disorder) | Short stature due to GHSR deficiency | Ghrelin receptor deficiency
+BMGC_DS17148,BMG_DS065969,766818009,X-linked non progressive cerebellar ataxia,,,,,,,C4707849,,,,,X-linked non progressive cerebellar ataxia (disorder) | X-linked non progressive cerebellar ataxia | X-linked spinocerebellar ataxia type 5
+BMGC_DS17149,BMG_DS065971,766821006,"Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome",,,,,,,C4707851,,,,,"Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome (disorder) | Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome"
+BMGC_DS17150,BMG_DS065974,766871009,Diencephalic mesencephalic junction dysplasia,,,,,,,C4707858,,,MONDO:0017868,diencephalic-mesencephalic junction dysplasia,Diencephalic mesencephalic junction dysplasia (disorder) | Diencephalic mesencephalic junction dysplasia
+BMGC_DS17151,BMG_DS065977,766879006,Combined immunodeficiency due to OX40 deficiency,,,,,,,C4707864,,,,,Combined immunodeficiency due to OX40 deficiency | Combined immunodeficiency due to OX40 deficiency (disorder) | Combined immunodeficiency with childhood-onset Kaposi sarcoma
+BMGC_DS17152,BMG_DS065978,766883006,Familial dilated cardiomyopathy with conduction defect due to LMNA mutation,,,,,,,C4707865,,,,,Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder)
+BMGC_DS17153,BMG_DS065980,766931003,Hypomyelination neuropathy arthrogryposis syndrome,,,,,,,C4707882,,,,,Hypomyelination neuropathy arthrogryposis syndrome (disorder) | Hypomyelination neuropathy arthrogryposis syndrome
+BMGC_DS17154,BMG_DS065983,,,,,,,,,C4707885,,,MONDO:0017112,isolated unilateral hemispheric cerebellar hypoplasia,
+BMGC_DS17155,BMG_DS065986,766977007,Severe early-onset axonal neuropathy due to mitofusin 2 deficiency,,,,,,,C4707897,,,MONDO:0019549,severe early-onset axonal neuropathy due to MFN2 deficiency,Severe early-onset axonal neuropathy due to MFN2 (mitofusin 2) deficiency | Severe early-onset axonal neuropathy due to MFN2 deficiency | Autosomal recessive Charcot-Marie-Tooth disease Ouvrier type | Severe early-onset axonal neuropathy due to mitofusin 2 deficiency (disorder) | Severe early-onset axonal neuropathy due to mitofusin 2 deficiency
+BMGC_DS17156,BMG_DS065991,766705006,Immunodeficiency due to ficolin 3 deficiency,,,,,,,C4707940,,,,,Immunodeficiency due to ficolin-3 deficiency | Immunodeficiency due to ficolin 3 deficiency (disorder) | Immunodeficiency due to ficolin 3 deficiency
+BMGC_DS17157,BMG_DS066017,767657005,Anemia due to and following chemotherapy,,,,,,,C4708167,,,,,Anemia due to and following chemotherapy | Anemia due to and following chemotherapy (disorder) | Anaemia due to and following chemotherapy
+BMGC_DS17158,BMG_DS066048,768473009,PURA syndrome,,,,,,,C4708498,,,,,"Purine rich element binding protein A syndrome | PURA-related neurodevelopmental disorder | PURA (purine rich element binding protein A) syndrome | Purine rich element binding protein A syndrome (disorder) | PURA syndrome | PURA-related severe neonatal hypotonia, seizure, encephalopathy syndrome"
+BMGC_DS17159,BMG_DS066052,768555009,5q31.3 microdeletion syndrome,,,,,,,C4708510,,,MONDO:0017811,severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion,"Severe neonatal hypotonia, seizures, encephalopathy syndrome due to 5q31.3 microdeletion | 5q31.3 microdeletion syndrome (disorder) | 5q31.3 microdeletion syndrome"
+BMGC_DS17160,BMG_DS066077,,,,,,,,,C4708599,,,MONDO:0020354,coloboma of choroid and retina,
+BMGC_DS17161,BMG_DS066092,769167005,Vaso-occlusive pain episode in sickle cell disease,,,,,,,C4708695,,,,,Vaso-occlusive pain co-occurrent and due to sickle cell disease (disorder) | Vaso-occlusive pain episode in sickle cell disease | Vaso-occlusive pain co-occurrent and due to sickle cell disease | Vasoocclusive pain episode in sickle cell disease
+BMGC_DS17162,BMG_DS066184,14619009,Heterophoria,Strabismus,9C80.4,Heterophoria,H50.5,,,C4721400,D013285,,,,Latent squint | Phoria | Phoria (disorder)
+BMGC_DS17163,BMG_DS066185,,"Angioma serpiginosum, X-linked",,,,,,,C4721404,C536366,300652,MONDO:0010391,"angioma serpiginosum, X-linked",
+BMGC_DS17164,BMG_DS066188,,,,,,,,,C4721414,,,MONDO:0018876,mantle cell lymphoma,
+BMGC_DS17165,BMG_DS066189,,,,,,,,,C4721429,,188550,MONDO:0008567,"thyroid cancer, nonmedullary, 1",
+BMGC_DS17166,BMG_DS066190,,"NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE",,,,,,,C4721436,,129010;605253,MONDO:0011527,Charcot-Marie-Tooth disease type 4E,
+BMGC_DS17167,BMG_DS066191,,"Charcot-Marie-Tooth disease, Type 4E",,,,,,,C4721437,C535301,,,,
+BMGC_DS17168,BMG_DS066196,,Peripheral Nervous System Diseases,Peripheral Nervous System Diseases,,,,,,C4721453,D010523,,,,
+BMGC_DS17169,BMG_DS066197,773985008,Peripheral dysostosis,,,,,,,C4721502,,170700,MONDO:0008227,peripheral dysostosis,Peripheral dysostosis (disorder) | Peripheral dysostosis
+BMGC_DS17170,BMG_DS066199,,"Alveolitis, Fibrosing",Pulmonary Fibrosis,,,,,,C4721507,D011658,,,,
+BMGC_DS17171,BMG_DS066200,,Usual Interstitial Pneumonia,Idiopathic Pulmonary Fibrosis,,,,,,C4721509,D054990,,,,
+BMGC_DS17172,BMG_DS066201,,,,,,,,,C4721532,,605027,MONDO:0011508,"lymphoma, non-Hodgkin, familial",
+BMGC_DS17173,BMG_DS066202,,PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER),,,,,DOID:0080476,peroxisome biogenesis disorder 1A,C4721541,,214100;602136,MONDO:0008953,peroxisome biogenesis disorder 1A (Zellweger),
+BMGC_DS17174,BMG_DS066203,770791000,Autosomal dominant neovascular inflammatory vitreoretinopathy,,,,,,,C4721549,,193235,MONDO:0100450,CAPN5-related vitreoretinopathy,Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) | Autosomal dominant neovascular inflammatory vitreoretinopathy
+BMGC_DS17175,BMG_DS066204,68784009;408335007,Autoimmune hepatitis,,DB96.0,Autoimmune hepatitis,K75.4,,,C4721555,,MTHU067664,MONDO:0016264,autoimmune hepatitis,Chronic active hepatitis | Chronic active hepatitis (disorder) | Autoimmune hepatitis (disorder) | Autoimmune hepatitis
+BMGC_DS17176,BMG_DS066205,,,,,,,,,C4721610,,,MONDO:0005140,ovarian carcinoma,
+BMGC_DS17177,BMG_DS066207,,Citrullinemia Type 1,Citrullinemia,,,,,,C4721769,D020159,215700,MONDO:0008988,citrullinemia type I,
+BMGC_DS17178,BMG_DS066210,,,,,,,,,C4721806,,,MONDO:0005341,skin basal cell carcinoma,
+BMGC_DS17179,BMG_DS066212,,"Marfan Syndrome, Type I",Marfan Syndrome,,,,,,C4721845,D008382,,,,
+BMGC_DS17180,BMG_DS066213,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 1",,,,,,,C4721885,,603511;611332,MONDO:0021018,autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6),
+BMGC_DS17181,BMG_DS066214,,"MYOPATHY, MYOFIBRILLAR, 4",,,,,DOID:0080095,myofibrillar myopathy 4,C4721886,,605906;609452,MONDO:0012277,myofibrillar myopathy 4,
+BMGC_DS17182,BMG_DS066215,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A",,,,,,,C4721887,,609260,MONDO:0012231,Charcot-Marie-Tooth disease type 2A2,
+BMGC_DS17183,BMG_DS066216,,Congenital External Ophthalmoplegia,,,,,DOID:0080143,congenital fibrosis of the extraocular muscles,C4721888,C580012,,,,
+BMGC_DS17184,BMG_DS066217,,SPERMATOGENIC FAILURE 3,,,,,DOID:0070168,spermatogenic failure 3,C4721889,,606766;608480,MONDO:0011720,spermatogenic failure 3,
+BMGC_DS17185,BMG_DS066218,,"CATARACT 2, MULTIPLE TYPES",,,,,,,C4721890,,604307,MONDO:0100436,"cataract 2, multiple types",
+BMGC_DS17186,BMG_DS066219,,"HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT",,,,,,,C4721891,,248190;610036,MONDO:0009548,renal hypomagnesemia 5 with ocular involvement,
+BMGC_DS17187,BMG_DS066221,,POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 1,,,,,,,C4721893,,604142;221770,MONDO:0020749,polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1,
+BMGC_DS17188,BMG_DS066222,,Hereditary Motor-Sensory Neuropathy with Pyramidal Signs,"Spastic Paraplegia, Hereditary",,,,,,C4721916,D015419,600361,MONDO:0010877,Charcot-Marie-Tooth disease type 5,
+BMGC_DS17189,BMG_DS066224,,Familial Idiopathic Pulmonary Fibrosis,Idiopathic Pulmonary Fibrosis,,,,,,C4721952,D054990,,,,
+BMGC_DS17190,BMG_DS066228,,Hypoprothrombinemias,Hypoprothrombinemias,,,,,,C4722227,D007020,,MONDO:0024307,prothrombin deficiency,
+BMGC_DS17191,BMG_DS066229,,,,,,,,,C4722258,,618231,MONDO:0032614,"epidermodysplasia verruciformis, susceptibility to, 2",
+BMGC_DS17192,BMG_DS066230,,"ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IV",,,,,,,C4722273,,618157;139191,MONDO:0032567,"isolated growth hormone deficiency, type 4",
+BMGC_DS17193,BMG_DS066232,,"NEUROPATHY, CONGENITAL HYPOMYELINATING, 2",,,,,,,C4722277,,159440;618184,MONDO:0020765,"neuropathy, congenital hypomyelinating, 2",
+BMGC_DS17194,BMG_DS066234,,"HYPER-IgE RECURRENT INFECTION SYNDROME 2, AUTOSOMAL RECESSIVE",,,,,DOID:0080594,hyper IgE recurrent infection syndrome 2,C4722305,,243700,MONDO:0009478,combined immunodeficiency due to DOCK8 deficiency,
+BMGC_DS17195,BMG_DS066237,,,,,,,,,C4722327,,601518,MONDO:0011098,"prostate cancer, hereditary, 1",
+BMGC_DS17196,BMG_DS066239,,Generalized Thyroid Hormone Resistance,Thyroid Hormone Resistance Syndrome,,,,,,C4722330,D018382,,MONDO:0009043,generalized resistance to thyroid hormone,
+BMGC_DS17197,BMG_DS066242,,MOYAMOYA DISEASE 6 WITH ACHALASIA,,,,,,,C4722422,,139396,,,
+BMGC_DS17198,BMG_DS066243,,"ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION",,,,,,,C4722446,,608329;618113,MONDO:0020853,"encephalitis/encephalopathy, mild, with reversible myelin vacuolization",
+BMGC_DS17199,BMG_DS066244,773646003,PLCG2-associated antibody deficiency and immune dysregulation,,,,,,,C4722480,,,,,PLCG2-associated antibody deficiency and immune dysregulation | PLCG2 (phospholipase C gamma 2) associated antibody deficiency and immune dysregulation | Phospholipase C gamma 2 associated antibody deficiency and immune dysregulation (disorder) | Phospholipase C gamma 2 associated antibody deficiency and immune dysregulation | FACU - familial atypical cold urticaria | Familial cold urticaria with common variable immunodeficiency
+BMGC_DS17200,BMG_DS066247,,,,,,,,,C4722564,,226400,MONDO:0100045,"epidermodysplasia verruciformis, susceptibility to, 1",
+BMGC_DS17201,BMG_DS066252,,,,,,,,,C4727832,,,MONDO:0100137,telomere syndrome,
+BMGC_DS17202,BMG_DS066256,,,,,,,,,C4728213,,,MONDO:1040002,PIK3CA-related overgrowth spectrum,
+BMGC_DS17203,BMG_DS066278,,LYMPHATIC MALFORMATION 5,,,,,,,C4746631,,153200,MONDO:0007920,lymphatic malformation 5,
+BMGC_DS17204,BMG_DS066279,,"ALPORT SYNDROME 2, AUTOSOMAL RECESSIVE",,,,,DOID:0110033,autosomal recessive Alport syndrome,C4746745,,203780;120131,MONDO:0008762,autosomal recessive Alport syndrome,
+BMGC_DS17205,BMG_DS066280,,"MICROCEPHALY, GROWTH RESTRICTION, AND INCREASED SISTER CHROMATID EXCHANGE 1",,,,,,,C4746755,,210900,,,
+BMGC_DS17206,BMG_DS066281,,ORTHOSTATIC HYPOTENSION 1,,,,,,,C4746777,,223360;609312,MONDO:0009123,orthostatic hypotension 1,
+BMGC_DS17207,BMG_DS066284,,,,,,,,,C4746851,,256040,MONDO:0054698,proteasome-associated autoinflammatory syndrome 1,
+BMGC_DS17208,BMG_DS066290,,,,,,,,,C4746956,,301014,MONDO:0049223,"osteogenesis imperfecta, type 19",
+BMGC_DS17209,BMG_DS066291,,"HEMOLYTIC ANEMIA, CONGENITAL, X-LINKED",,,,,DOID:0111846,X-linked congenital hemolytic anemia,C4746970,,300516;301015,MONDO:0060455,X-linked congenital hemolytic anemia,
+BMGC_DS17210,BMG_DS066292,,"DEAFNESS, X-LINKED 7",,,,,DOID:0111738,X-linked deafness 7,C4746975,,300969;301018,MONDO:0044702,X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome,
+BMGC_DS17211,BMG_DS066293,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12",,,,,DOID:0112099,nuclear type mitochondrial complex I deficiency 12,C4746984,,300078;301020,MONDO:0026720,"mitochondrial complex 1 deficiency, nuclear type 12",
+BMGC_DS17212,BMG_DS066294,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 30",,,,,DOID:0112098,nuclear type mitochondrial complex I deficiency 30,C4746985,,301021;300403,MONDO:0026721,"mitochondrial complex 1 deficiency, nuclear type 30",
+BMGC_DS17213,BMG_DS066295,,"ALPORT SYNDROME 1, X-LINKED",,,,,DOID:0110034,X-linked Alport syndrome,C4746986,,301050;303630,MONDO:0010520,X-linked Alport syndrome,
+BMGC_DS17214,BMG_DS066296,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, MITOCHONDRIAL TYPE 1",,,,,DOID:0112101,mitochondrial type mitochondrial complex I deficiency 1,C4746992,,500014;516002,MONDO:0027068,"mitochondrial complex 1 deficiency, mitochondrial type 1",
+BMGC_DS17215,BMG_DS066297,,CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 1,,,,,,,C4747394,,139150;608354;608355;608354,MONDO:0020783,capillary malformation-arteriovenous malformation 1,
+BMGC_DS17216,BMG_DS066298,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20",,,,,,,C4747517,,611103;611126,MONDO:0012624,acyl-CoA dehydrogenase 9 deficiency,
+BMGC_DS17217,BMG_DS066299,,LYMPHATIC MALFORMATION 2,,,,,DOID:0070211,hereditary lymphedema IB,C4747568,,611944,MONDO:0012765,lymphatic malformation 2,
+BMGC_DS17218,BMG_DS066301,,LYMPHATIC MALFORMATION 3,,,,,DOID:0070208,hereditary lymphedema IC,C4747646,,608803;613480,MONDO:0013278,lymphatic malformation 3,
+BMGC_DS17219,BMG_DS066302,,,,,,,,,C4747658,,,MONDO:0800356,"short-rib thoracic dysplasia 7/20 with polydactyly, digenic",
+BMGC_DS17220,BMG_DS066303,,,,,,,,,C4747715,,615290,MONDO:0014121,autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures,
+BMGC_DS17221,BMG_DS066304,,RETINITIS PIGMENTOSA 82 WITH OR WITHOUT SITUS INVERSUS,,,,,,,C4747737,,615434;615407,MONDO:0014186,retinitis pigmentosa with or without situs inversus,
+BMGC_DS17222,BMG_DS066305,,IMMUNODEFICIENCY 15B,,,,,DOID:0111959,immunodeficiency 15B,C4747743,,603258;615592,MONDO:0014267,severe combined immunodeficiency due to IKK2 deficiency,
+BMGC_DS17223,BMG_DS066306,,LYMPHATIC MALFORMATION 4,,,,,DOID:0070209,hereditary lymphedema ID,C4747769,,601528;615907,MONDO:0014393,lymphatic malformation 4,
+BMGC_DS17224,BMG_DS066308,,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3,,,,,DOID:0060916,proteasome-associated autoinflammatory syndrome 3,C4747850,,617591,MONDO:0054699,proteasome-associated autoinflammatory syndrome 3,
+BMGC_DS17225,BMG_DS066309,,"HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES",,,,,,,C4747885,,617967;614218,MONDO:0054794,"hydrocephalus, congenital, 3, with brain anomalies",
+BMGC_DS17226,BMG_DS066310,,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17,,,,,,,C4747891,,600154;618010,MONDO:0060724,glycosylphosphatidylinositol biosynthesis defect 17,
+BMGC_DS17227,BMG_DS066311,1237412001,Regressive spondylometaphyseal dysplasia,,,,,,,C4747922,,618019,MONDO:0018663,regressive spondylometaphyseal dysplasia,Regressive spondylometaphyseal dysplasia | Regressive spondylometaphyseal dysplasia (disorder)
+BMGC_DS17228,BMG_DS066312,,TETRAAMELIA SYNDROME 2,,,,,DOID:0112193,tetraamelia syndrome 2,C4747923,,610575;618021,MONDO:0060732,tetraamelia syndrome 2,
+BMGC_DS17229,BMG_DS066313,,,,,,,,,C4747940,,618022,MONDO:0060733,humerofemoral hypoplasia with radiotibial ray deficiency,
+BMGC_DS17230,BMG_DS066314,,COFFIN-SIRIS SYNDROME 7,,,,,DOID:0112369,Coffin-Siris syndrome 7,C4747954,,618027;601671,MONDO:0054831,Coffin-Siris syndrome 7,
+BMGC_DS17231,BMG_DS066315,,"CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 4",,,,,DOID:0080669,posterior polymorphous corneal dystrophy 4,C4747961,,618031;608576,MONDO:0054832,"corneal dystrophy, posterior polymorphous, 4",
+BMGC_DS17232,BMG_DS066316,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2DD",,,,,DOID:0111558,Charcot-Marie-Tooth disease type 2DD,C4747974,,182310;618036,MONDO:0054833,"charcot-marie-tooth disease, axonal, type 2DD",
+BMGC_DS17233,BMG_DS066317,,IMMUNODEFICIENCY 100 WITH PULMONARY ALVEOLAR PROTEINOSIS AND HYPOGAMMAGLOBULINEMIA,,,,,,,C4747984,,164350;618042,MONDO:0020840,pulmonary alveolar proteinosis with hypogammaglobulinemia,
+BMGC_DS17234,BMG_DS066318,,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2,,,,,DOID:0060914,proteosome-associated autoinflammatory syndrome 2,C4747989,,613386;618048,MONDO:0054700,proteasome-associated autoinflammatory syndrome 2,
+BMGC_DS17235,BMG_DS066319,,,,,,,DOID:0070490,infantile parkinsonism-dystonia 2,C4747991,,,,,
+BMGC_DS17236,BMG_DS066320,,,,,,,,,C4748003,,618050,MONDO:0054837,"intellectual disability, autosomal dominant 57",
+BMGC_DS17237,BMG_DS066321,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 27",,,,,,,C4748014,,617608;618052,MONDO:0054838,"cardiomyopathy, familial hypertrophic 27",
+BMGC_DS17238,BMG_DS066322,,NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES,,,,,,,C4748032,,618056;614506,MONDO:0020841,neurodevelopmental disorder with cerebellar atrophy and with or without seizures,
+BMGC_DS17239,BMG_DS066323,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA,,,,,,,C4748041,,618060,MONDO:0060745,intellectual developmental disorder with or without epilepsy or cerebellar ataxia,
+BMGC_DS17240,BMG_DS066324,,POLYCYSTIC KIDNEY DISEASE 6 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE,,,,,DOID:0060951,polycystic kidney disease 6,C4748044,,618061;611341,MONDO:0054842,polycystic kidney disease 6 with or without polycystic liver disease,
+BMGC_DS17241,BMG_DS066325,,"CILIARY DYSKINESIA, PRIMARY, 38",,,,,DOID:0111852,primary ciliary dyskinesia 38,C4748052,,618058;618063,MONDO:0054843,"ciliary dyskinesia, primary, 38",
+BMGC_DS17242,BMG_DS066326,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 1D",,,,,DOID:0112323,pontocerebellar hypoplasia type 1D,C4748058,,606180;618065,MONDO:0054844,"pontocerebellar hypoplasia, type 1D",
+BMGC_DS17243,BMG_DS066327,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 66,,,,,DOID:0080446,developmental and epileptic encephalopathy 66,C4748070,,610423;618067,MONDO:0054845,"developmental and epileptic encephalopathy, 66",
+BMGC_DS17244,BMG_DS066328,,"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 6",,,,,DOID:0111696,familial adult myoclonic epilepsy 6,C4748079,,610739;618074,MONDO:0054846,"epilepsy, familial adult myoclonic, 6",
+BMGC_DS17245,BMG_DS066329,,"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 7",,,,,DOID:0111694,familial adult myoclonic epilepsy 7,C4748080,,618075;609530,MONDO:0054847,"epilepsy, familial adult myoclonic, 7",
+BMGC_DS17246,BMG_DS066330,,NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH,,,,,DOID:0070421,neurodevelopmental disorder with spasticity and poor growth,C4748081,,618076;610554,MONDO:0060752,neurodevelopmental disorder with spasticity and poor growth,
+BMGC_DS17247,BMG_DS066331,,INFLAMMATORY BOWEL DISEASE 29,,,,,DOID:0112155,inflammatory bowel disease 29,C4748083,,618077;618051,MONDO:0054849,inflammatory bowel disease 29,
+BMGC_DS17248,BMG_DS066332,,OVARIAN DYSGENESIS 6,,,,,DOID:0080498,ovarian dysgenesis 6,C4748084,,607617;618078,MONDO:0054850,ovarian dysgenesis 6,
+BMGC_DS17249,BMG_DS066333,,PEELING SKIN SYNDROME 6,,,,,DOID:0070525,peeling skin syndrome 6,C4748093,,616284;618084,MONDO:0054852,peeling skin syndrome 6,
+BMGC_DS17250,BMG_DS066334,,SPERMATOGENIC FAILURE 28,,,,,DOID:0111916,spermatogenic failure 28,C4748117,,609644;618086,MONDO:0054732,spermatogenic failure 28,
+BMGC_DS17251,BMG_DS066336,,"SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS",,,,,,,C4748120,,604065;618087,MONDO:0060758,"spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits",
+BMGC_DS17252,BMG_DS066337,,"NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES",,,,,DOID:0081327,"neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures",C4748127,,618088;611720,MONDO:0060759,"neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures",
+BMGC_DS17253,BMG_DS066338,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES,,,,,,,C4748135,,607871;618089,MONDO:0060760,intellectual developmental disorder with dysmorphic facies and behavioral abnormalities,
+BMGC_DS17254,BMG_DS066339,,NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM,,,,,,,C4748137,,610236;618090,MONDO:0060761,neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum,
+BMGC_DS17255,BMG_DS066340,,SPERMATOGENIC FAILURE 29,,,,,DOID:0111930,spermatogenic failure 29,C4748142,,605753;618091,MONDO:0054733,spermatogenic failure 29,
+BMGC_DS17256,BMG_DS066341,,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES",,,,,,,C4748152,,618092,MONDO:0060763,"intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities",
+BMGC_DS17257,BMG_DS066342,,SPINOCEREBELLAR ATAXIA 48,,,,,DOID:0111746,cerebellar ataxia type 48,C4748158,,607207;618093,MONDO:0032526,spinocerebellar ataxia 48,
+BMGC_DS17258,BMG_DS066343,,"DEAFNESS, AUTOSOMAL RECESSIVE 110",,,,,DOID:0111644,autosomal recessive nonsyndromic deafness 110,C4748162,,603196;618094,MONDO:0054860,"hearing loss, autosomal recessive 110",
+BMGC_DS17259,BMG_DS066344,,,,,,,,,C4748167,,618095,MONDO:0054861,"intellectual disability, autosomal recessive 63",
+BMGC_DS17260,BMG_DS066345,,PREMATURE OVARIAN FAILURE 15,,,,,DOID:0080872,primary ovarian insufficiency 15,C4748170,,618096;609644,MONDO:0054862,premature ovarian failure 15,
+BMGC_DS17261,BMG_DS066346,,"MICROCEPHALY, GROWTH RESTRICTION, AND INCREASED SISTER CHROMATID EXCHANGE 2",,,,,,,C4748176,,601243;618097,MONDO:0020628,"microcephaly, growth restriction, and increased sister chromatid exchange 2",
+BMGC_DS17262,BMG_DS066347,,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5",,,,,DOID:0111524,autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5,C4748184,,601243;618098,MONDO:0020845,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5",
+BMGC_DS17263,BMG_DS066348,,,,,,,,,C4748192,,618103,MONDO:0020846,"intellectual disability, autosomal recessive 64",
+BMGC_DS17264,BMG_DS066349,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 58",,,,,,,C4748195,,618106;600960,MONDO:0020847,"intellectual disability, autosomal dominant 58",
+BMGC_DS17265,BMG_DS066350,,"OSTEOPETROSIS, AUTOSOMAL DOMINANT 3",,,,,,,C4748197,,611466;618107,MONDO:0020848,"osteopetrosis, autosomal dominant 3",
+BMGC_DS17266,BMG_DS066351,,IMMUNODEFICIENCY 57 WITH AUTOINFLAMMATION,,,,,DOID:0111952,immunodeficiency 57,C4748212,,618108;603453,MONDO:0020849,immunodeficiency 57,
+BMGC_DS17267,BMG_DS066352,,,,,,,,,C4748219,,618109,MONDO:0020850,"intellectual disability, autosomal recessive 65",
+BMGC_DS17268,BMG_DS066353,,SPERMATOGENIC FAILURE 30,,,,,DOID:0111913,spermatogenic failure 30,C4748224,,617963;618110,MONDO:0020851,spermatogenic failure 30,
+BMGC_DS17269,BMG_DS066354,,SPERMATOGENIC FAILURE 31,,,,,DOID:0111922,spermatogenic failure 31,C4748234,,618085;618112,MONDO:0020852,spermatogenic failure 31,
+BMGC_DS17270,BMG_DS066355,,LIDDLE SYNDROME 2,,,,,,,C4748251,,600761;618114,MONDO:0020854,Liddle syndrome 2,
+BMGC_DS17271,BMG_DS066356,,SPERMATOGENIC FAILURE 32,,,,,DOID:0111925,spermatogenic failure 32,C4748253,,610224;618115,MONDO:0020855,spermatogenic failure 32,
+BMGC_DS17272,BMG_DS066357,,BONE MARROW FAILURE SYNDROME 4,,,,,,,C4748257,,612176;618116,MONDO:0020856,bone marrow failure syndrome 4,
+BMGC_DS17273,BMG_DS066359,,OVARIAN DYSGENESIS 7,,,,,DOID:0080499,ovarian dysgenesis 7,C4748263,,618117;605810,MONDO:0020857,ovarian dysgenesis 7,
+BMGC_DS17274,BMG_DS066360,,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5",,,,,DOID:0070463,mitochondrial complex V (ATP synthase) deficiency nuclear type 5,C4748269,,603150;618120,MONDO:0020858,mitochondrial complex 5 (ATP synthase) deficiency nuclear type 5,
+BMGC_DS17275,BMG_DS066361,,,,,,,,,C4748277,,618123,MONDO:0029130,"polydactyly, postaxial, type A8",
+BMGC_DS17276,BMG_DS066362,,"PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT",,,,,,,C4748283,,603294;618124,MONDO:0029131,"peripheral neuropathy, autosomal recessive, with or without impaired intellectual development",
+BMGC_DS17277,BMG_DS066363,,LIDDLE SYNDROME 3,,,,,,,C4748292,,600228;618126,MONDO:0029132,Liddle syndrome 3,
+BMGC_DS17278,BMG_DS066364,1279886003,Calpain-3-related limb girdle muscular dystrophy D4,,,,,,,C4748295,,618129,MONDO:0029133,"muscular dystrophy, limb-girdle, autosomal dominant 4",Calpain-3-related limb girdle muscular dystrophy D4 | Calpain-3-related limb girdle muscular dystrophy D4 (disorder) | Limb girdle muscular dystrophy type D4
+BMGC_DS17279,BMG_DS066365,,IMMUNODEFICIENCY 58,,,,,DOID:0111984,immunodeficiency 58,C4748304,,610859;618131,MONDO:0029134,severe combined immunodeficiency due to CARMIL2 deficiency,
+BMGC_DS17280,BMG_DS066366,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8",,,,,DOID:0112382,muscular dystrophy-dystroglycanopathy type C8,C4748320,,618135;614828,MONDO:0029135,"muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8",
+BMGC_DS17281,BMG_DS066367,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23",,,,,,,C4748327,,156225;618138,MONDO:0029136,"muscular dystrophy, limb-girdle, autosomal recessive 23",
+BMGC_DS17282,BMG_DS066368,,"DEAFNESS, AUTOSOMAL DOMINANT 74",,,,,DOID:0112165,autosomal dominant nonsyndromic deafness 74,C4748334,,618140;602987,MONDO:0029137,"hearing loss, autosomal dominant 74",
+BMGC_DS17283,BMG_DS066369,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 67,,,,,DOID:0112203,developmental and epileptic encephalopathy 67,C4748341,,610648;618141,MONDO:0029138,"developmental and epileptic encephalopathy, 67",
+BMGC_DS17284,BMG_DS066370,,"MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME",,,,,,,C4748348,,617057;618142,MONDO:0020647,"microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome",
+BMGC_DS17285,BMG_DS066371,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 95,,,,,DOID:0070382,developmental and epileptic encephalopathy 95,C4748357,,610271;618143,MONDO:0029140,glycosylphosphatidylinositol biosynthesis defect 18,
+BMGC_DS17286,BMG_DS066372,,"USHER SYNDROME, TYPE IV",,,,,,,C4748364,,610008;618144,MONDO:0029141,"Usher syndrome, type 4",
+BMGC_DS17287,BMG_DS066373,,"DEAFNESS, AUTOSOMAL RECESSIVE 111",,,,,DOID:0111640,autosomal recessive nonsyndromic deafness 111,C4748374,,604873;618145,MONDO:0029142,"hearing loss, autosomal recessive 111",
+BMGC_DS17288,BMG_DS066374,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES,,,,,,,C4748381,,618147;603544,MONDO:0029143,intellectual developmental disorder with hypertelorism and distinctive facies,
+BMGC_DS17289,BMG_DS066375,1269235004,Autosomal recessive extra-oral halitosis,,,,,,,C4748387,,618148,MONDO:0029144,extraoral halitosis due to methanethiol oxidase deficiency,Methanethiol oxidase deficiency | MTO (methanethiol oxidase) deficiency | Autosomal recessive extra-oral halitosis | Autosomal recessive extra-oral halitosis (disorder)
+BMGC_DS17290,BMG_DS066376,,SPERMATOGENIC FAILURE 33,,,,,DOID:0111915,spermatogenic failure 33,C4748395,,618152;618146,MONDO:0029147,spermatogenic failure 33,
+BMGC_DS17291,BMG_DS066377,,SPERMATOGENIC FAILURE 34,,,,,DOID:0111911,spermatogenic failure 34,C4748403,,615796;618153,MONDO:0029148,spermatogenic failure 34,
+BMGC_DS17292,BMG_DS066378,,HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 3,,,,,,,C4748408,,605011;618154,MONDO:0032564,hennekam lymphangiectasia-lymphedema syndrome 3,
+BMGC_DS17293,BMG_DS066379,,"OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES",,,,,,,C4748418,,159990;618155,MONDO:0032565,"ophthalmoplegia, external, with rib and vertebral anomalies",
+BMGC_DS17294,BMG_DS066380,,SQUALENE SYNTHASE DEFICIENCY,,,,,,,C4748427,,184420;618156,MONDO:0032566,squalene synthase deficiency,
+BMGC_DS17295,BMG_DS066381,,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY",,,,,,,C4748428,,602590;618158,MONDO:0032568,"intellectual developmental disorder with macrocephaly, seizures, and speech delay",
+BMGC_DS17296,BMG_DS066382,,"PITUITARY HORMONE DEFICIENCY, COMBINED OR ISOLATED, 7",,,,,DOID:0061016,combined or isolated pituitary growth hormone deficiency 7,C4748435,,618160,MONDO:0032569,"isolated growth hormone deficiency, type 5",
+BMGC_DS17297,BMG_DS066383,,JOUBERT SYNDROME 35,,,,,,,C4748442,,618161;604695,MONDO:0032570,Joubert syndrome 35,
+BMGC_DS17298,BMG_DS066384,,"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE",,,,,,,C4748455,,618162;614776,MONDO:0032571,"spondyloepimetaphyseal dysplasia, Krakow type",
+BMGC_DS17299,BMG_DS066385,,,,,,,,,C4748484,,618164,MONDO:0032572,"cardiac, facial, and digital anomalies with developmental delay",
+BMGC_DS17300,BMG_DS066386,,BONE MARROW FAILURE SYNDROME 5,,,,,,,C4748488,,191170;618165,MONDO:0032573,bone marrow failure syndrome 5,
+BMGC_DS17301,BMG_DS066387,,"OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS",,,,,,,C4748496,,618167;610128,MONDO:0032574,"osteochondrodysplasia, brachydactyly, and overlapping malformed digits",
+BMGC_DS17302,BMG_DS066388,,DIARRHEA 9,,,,,,,C4748517,,618168;601968,MONDO:0032575,diarrhea 9,
+BMGC_DS17303,BMG_DS066389,,"NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES",,,,,DOID:0070352,stress-induced childhood-onset neurodegeneration with variable ataxia and seizures,C4748527,,618170;610624,MONDO:0100095,"neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures",
+BMGC_DS17304,BMG_DS066390,,RETINITIS PIGMENTOSA 83,,,,,DOID:0112140,retinitis pigmentosa 83,C4748536,,618173;604695,MONDO:0032577,retinitis pigmentosa 83,
+BMGC_DS17305,BMG_DS066391,,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9",,,,,,,C4748540,,618174;114025,MONDO:0032578,"cortical dysplasia, complex, with other brain malformations 9",
+BMGC_DS17306,BMG_DS066392,,"NEPHROTIC SYNDROME, TYPE 17",,,,,DOID:0080392,nephrotic syndrome type 17,C4748545,,170285;618176,MONDO:0032580,"nephrotic syndrome, type 17",
+BMGC_DS17307,BMG_DS066393,,"NEPHROTIC SYNDROME, TYPE 18",,,,,DOID:0080393,nephrotic syndrome type 18,C4748549,,618177;607613,MONDO:0032581,"nephrotic syndrome, type 18",
+BMGC_DS17308,BMG_DS066394,,"NEPHROTIC SYNDROME, TYPE 19",,,,,DOID:0080394,nephrotic syndrome type 19,C4748552,,607614;618178,MONDO:0032582,"nephrotic syndrome, type 19",
+BMGC_DS17309,BMG_DS066395,,"MICROCEPHALY 24, PRIMARY, AUTOSOMAL RECESSIVE",,,,,,,C4748555,,609264;618179,MONDO:0032583,"microcephaly 24, primary, autosomal recessive",
+BMGC_DS17310,BMG_DS066396,,"ECTODERMAL DYSPLASIA 14, HAIR/TOOTH TYPE, WITH OR WITHOUT HYPOHIDROSIS",,,,,DOID:0111662,ectodermal dysplasia 14,C4748560,,618180,MONDO:0032584,"ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis",
+BMGC_DS17311,BMG_DS066399,,ORTHOSTATIC HYPOTENSION 2,,,,,,,C4748569,,600019;618182,MONDO:0020751,orthostatic hypotension 2,
+BMGC_DS17312,BMG_DS066400,,"DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE",,,,,,,C4748579,,607647;618183,MONDO:0032586,"diarrhea 10, protein-losing enteropathy type",
+BMGC_DS17313,BMG_DS066401,,PERIVENTRICULAR NODULAR HETEROTOPIA 8,,,,,,,C4748602,,618185;103180,MONDO:0032588,periventricular nodular heterotopia 8,
+BMGC_DS17314,BMG_DS066402,,"NEUROPATHY, CONGENITAL HYPOMYELINATING, 3",,,,,,,C4748608,,602346;618186,MONDO:0020766,"neuropathy, congenital hypomyelinating, 3",
+BMGC_DS17315,BMG_DS066403,,OVARIAN DYSGENESIS 8,,,,,DOID:0080500,ovarian dysgenesis 8,C4748626,,601663;618187,MONDO:0032590,ovarian dysgenesis 8,
+BMGC_DS17316,BMG_DS066404,,"CARDIOMYOPATHY, DILATED, 2C",,,,,DOID:0081159,dilated cardiomyopathy 2C,C4748647,,618189;609853,MONDO:0032592,"cardiomyopathy, dilated, 2c",
+BMGC_DS17317,BMG_DS066405,,POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2,,,,,,,C4748657,,605086;618193,MONDO:0020750,polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2,
+BMGC_DS17318,BMG_DS066406,,INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA,,,,,,,C4748658,,618195;611611,MONDO:0032594,intellectual developmental disorder and retinitis pigmentosa; IDDRP,
+BMGC_DS17319,BMG_DS066407,,CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 2,,,,,,,C4748670,,618196;600011,MONDO:0020785,capillary malformation-arteriovenous malformation 2,
+BMGC_DS17320,BMG_DS066408,,"MYASTHENIC SYNDROME, CONGENITAL, 23, PRESYNAPTIC",,,,,,,C4748678,,618197;190315,MONDO:0032596,"myasthenic syndrome, congenital, 23, presynaptic",
+BMGC_DS17321,BMG_DS066409,,"MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC",,,,,,,C4748684,,618198,MONDO:0032597,"myasthenic syndrome, congenital, 24, presynaptic",
+BMGC_DS17322,BMG_DS066410,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 68,,,,,DOID:0112204,developmental and epileptic encephalopathy 68,C4748688,,608112;618201,MONDO:0032598,"developmental and epileptic encephalopathy, 68",
+BMGC_DS17323,BMG_DS066411,,IMMUNODEFICIENCY 15A,,,,,DOID:0111960,immunodeficiency 15A,C4748694,,603258;618204,MONDO:0032599,immunodeficiency 15a,
+BMGC_DS17324,BMG_DS066412,1179408008,Snijders Blok-Campeau syndrome,,,,,,,C4748701,C000729467,618205,MONDO:0032600,Snijders Blok-Campeau syndrome,"Chromodomain helicase dna-binding protein 3- related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome | CHD3-related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome | Snijders Blok-Campeau syndrome | Chromodomain helicase dna-binding protein 3- related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome (disorder)"
+BMGC_DS17325,BMG_DS066413,,"INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY",,,,,,,C4748708,,618213;190180,MONDO:0032601,"inflammatory bowel disease, immunodeficiency, and encephalopathy",
+BMGC_DS17326,BMG_DS066414,1217371005,"Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome",,,,,,,C4748715,,618218,MONDO:0033864,infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome,"Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder) | Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome | SYT1-related neurodevelopmental disorder | Synaptotagmin 1-related neurodevelopmental disorder | Baker Gordon syndrome"
+BMGC_DS17327,BMG_DS066415,,,,,,,,,C4748721,,618219,MONDO:0032603,"polydactyly, postaxial, type A9",
+BMGC_DS17328,BMG_DS066416,,RETINITIS PIGMENTOSA 84,,,,,DOID:0112141,retinitis pigmentosa 84,C4748725,,618220;605584,MONDO:0032604,retinitis pigmentosa 84,
+BMGC_DS17329,BMG_DS066417,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 66",,,,,DOID:0081227,autosomal recessive intellectual developmental disorder 66,C4748732,,616082;618221,MONDO:0032605,"intellectual disability, autosomal recessive 66",
+BMGC_DS17330,BMG_DS066418,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2",,,,,DOID:0112083,nuclear type mitochondrial complex I deficiency 2,C4748737,,602141;618222,MONDO:0032606,"mitochondrial complex 1 deficiency, nuclear type 2",
+BMGC_DS17331,BMG_DS066419,,VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION,,,,,DOID:0070345,vertebral anomalies and variable endocrine and T-cell dysfunction,C4748741,,618223;600747,MONDO:0032607,vertebral anomalies and variable endocrine and T-cell dysfunction,
+BMGC_DS17332,BMG_DS066420,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3",,,,,DOID:0112093,nuclear type mitochondrial complex I deficiency 3,C4748752,,601825;618224,MONDO:0032608,"mitochondrial complex 1 deficiency, nuclear type 3",
+BMGC_DS17333,BMG_DS066421,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4",,,,,DOID:0112082,nuclear type mitochondrial complex I deficiency 4,C4748753,,618225;161015,MONDO:0032609,"mitochondrial complex 1 deficiency, nuclear type 4",
+BMGC_DS17334,BMG_DS066422,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5",,,,,DOID:0112068,nuclear type mitochondrial complex I deficiency 5,C4748754,,618226;157655,MONDO:0032610,"mitochondrial complex 1 deficiency, nuclear type 5",
+BMGC_DS17335,BMG_DS066423,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6",,,,,DOID:0112066,nuclear type mitochondrial complex I deficiency 6,C4748759,,602985;618228,MONDO:0032611,"mitochondrial complex 1 deficiency, nuclear type 6",
+BMGC_DS17336,BMG_DS066424,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7",,,,,DOID:0112092,nuclear type mitochondrial complex I deficiency 7,C4748760,,600532;618229,MONDO:0032612,"mitochondrial complex 1 deficiency, nuclear type 7",
+BMGC_DS17337,BMG_DS066425,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 8",,,,,DOID:0112081,nuclear type mitochondrial complex I deficiency 8,C4748766,,603846;618230,MONDO:0032613,"mitochondrial complex 1 deficiency, nuclear type 8",
+BMGC_DS17338,BMG_DS066426,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 9",,,,,DOID:0112073,nuclear type mitochondrial complex I deficiency 9,C4748767,,618232;603848,MONDO:0032615,"mitochondrial complex 1 deficiency, nuclear type 9",
+BMGC_DS17339,BMG_DS066427,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10",,,,,DOID:0112075,nuclear type mitochondrial complex I deficiency 10,C4748768,,618233;609653,MONDO:0032616,"mitochondrial complex 1 deficiency, nuclear type 10",
+BMGC_DS17340,BMG_DS066428,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11",,,,,DOID:0112089,nuclear type mitochondrial complex I deficiency 11,C4748769,,606934;618234,MONDO:0032617,"mitochondrial complex 1 deficiency, nuclear type 11",
+BMGC_DS17341,BMG_DS066429,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13",,,,,DOID:0112076,nuclear type mitochondrial complex I deficiency 13,C4748770,,602137;618235,MONDO:0032618,"mitochondrial complex 1 deficiency, nuclear type 13",
+BMGC_DS17342,BMG_DS066430,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14",,,,,DOID:0112094,nuclear type mitochondrial complex I deficiency 14,C4748777,,612638;618236,MONDO:0032619,"mitochondrial complex 1 deficiency, nuclear type 14",
+BMGC_DS17343,BMG_DS066431,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15",,,,,DOID:0112077,nuclear type mitochondrial complex I deficiency 15,C4748778,,618237;611776,MONDO:0032620,"mitochondrial complex 1 deficiency, nuclear type 15",
+BMGC_DS17344,BMG_DS066433,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16",,,,,DOID:0112096,nuclear type mitochondrial complex I deficiency 16,C4748785,,612360;618238,MONDO:0032621,"mitochondrial complex 1 deficiency, nuclear type 16",
+BMGC_DS17345,BMG_DS066434,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17",,,,,DOID:0112078,nuclear type mitochondrial complex I deficiency 17,C4748786,,612392;618239,MONDO:0032622,"mitochondrial complex 1 deficiency, nuclear type 17",
+BMGC_DS17346,BMG_DS066435,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18",,,,,DOID:0112070,nuclear type mitochondrial complex I deficiency 18,C4748790,,612911;618240,MONDO:0032623,"mitochondrial complex 1 deficiency, nuclear type 18",
+BMGC_DS17347,BMG_DS066436,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19",,,,,DOID:0112085,nuclear type mitochondrial complex I deficiency 19,C4748791,,618241;613622,MONDO:0032624,"mitochondrial complex 1 deficiency, nuclear type 19",
+BMGC_DS17348,BMG_DS066437,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21",,,,,DOID:0112088,nuclear type mitochondrial complex I deficiency 21,C4748792,,618242;613621,MONDO:0032625,"mitochondrial complex 1 deficiency, nuclear type 21",
+BMGC_DS17349,BMG_DS066438,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22",,,,,DOID:0112069,nuclear type mitochondrial complex I deficiency 22,C4748796,,603835;618243,MONDO:0032626,"mitochondrial complex 1 deficiency, nuclear type 22",
+BMGC_DS17350,BMG_DS066439,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 23",,,,,DOID:0112087,nuclear type mitochondrial complex I deficiency 23,C4748799,,614530;618244,MONDO:0032627,"mitochondrial complex 1 deficiency, nuclear type 23",
+BMGC_DS17351,BMG_DS066440,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 24",,,,,DOID:0112079,nuclear type mitochondrial complex I deficiency 24,C4748803,,618245;601445,MONDO:0032628,"mitochondrial complex 1 deficiency, nuclear type 24",
+BMGC_DS17352,BMG_DS066441,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25",,,,,DOID:0112067,nuclear type mitochondrial complex I deficiency 25,C4748806,,618246;603839,MONDO:0032629,"mitochondrial complex 1 deficiency, nuclear type 25",
+BMGC_DS17353,BMG_DS066442,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26",,,,,DOID:0112086,nuclear type mitochondrial complex I deficiency 26,C4748809,,603834;618247,MONDO:0032630,"mitochondrial complex 1 deficiency, nuclear type 26",
+BMGC_DS17354,BMG_DS066443,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 27",,,,,DOID:0112090,nuclear type mitochondrial complex I deficiency 27,C4748826,,618248;611766,MONDO:0032631,"mitochondrial complex 1 deficiency, nuclear type 27",
+BMGC_DS17355,BMG_DS066444,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28",,,,,DOID:0112095,nuclear type mitochondrial complex I deficiency 28,C4748827,,618249;609435,MONDO:0032632,"mitochondrial complex 1 deficiency, nuclear type 28",
+BMGC_DS17356,BMG_DS066445,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 29",,,,,DOID:0112084,nuclear type mitochondrial complex I deficiency 29,C4748830,,618250;615533,MONDO:0032633,"mitochondrial complex 1 deficiency, nuclear type 29",
+BMGC_DS17357,BMG_DS066446,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 31",,,,,DOID:0112071,nuclear type mitochondrial complex I deficiency 31,C4748838,,615534;618251,MONDO:0032634,"mitochondrial complex 1 deficiency, nuclear type 31",
+BMGC_DS17358,BMG_DS066447,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 32",,,,,DOID:0112080,nuclear type mitochondrial complex I deficiency 32,C4748839,,602140;618252,MONDO:0032635,"mitochondrial complex 1 deficiency, nuclear type 32",
+BMGC_DS17359,BMG_DS066448,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33",,,,,DOID:0112097,nuclear type mitochondrial complex I deficiency 33,C4748840,,618253;602138,MONDO:0032636,"mitochondrial complex 1 deficiency, nuclear type 33",
+BMGC_DS17360,BMG_DS066449,,"CILIARY DYSKINESIA, PRIMARY, 39",,,,,DOID:0111854,primary ciliary dyskinesia 39,C4748841,,618254;618227,MONDO:0032637,"ciliary dyskinesia, primary, 39",
+BMGC_DS17361,BMG_DS066450,,"DEAFNESS, AUTOSOMAL RECESSIVE 112",,,,,DOID:0111637,autosomal recessive nonsyndromic deafness 112,C4748855,,607012;618257,MONDO:0032639,"hearing loss, autosomal recessive 112",
+BMGC_DS17362,BMG_DS066451,,MIRROR MOVEMENTS 4,,,,,,,C4748869,,601614;618264,MONDO:0032641,mirror movements 4,
+BMGC_DS17363,BMG_DS066453,,"ARTHROGRYPOSIS, CLEFT PALATE, CRANIOSYNOSTOSIS, AND IMPAIRED INTELLECTUAL DEVELOPMENT",,,,,,,C4748872,,114105;618265,MONDO:0032642,"arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development",
+BMGC_DS17364,BMG_DS066454,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 12",,,,,DOID:0112327,pontocerebellar hypoplasia type 12,C4748873,,618266;609855,MONDO:0032643,"pontocerebellar hypoplasia, type 12",
+BMGC_DS17365,BMG_DS066455,,,,,,,,,C4748876,,618267,MONDO:0032644,"epidermodysplasia verruciformis, susceptibility to, 3",
+BMGC_DS17366,BMG_DS066456,,TRICHOHEPATONEURODEVELOPMENTAL SYNDROME,,,,,,,C4748898,,618260;618268,MONDO:0032645,trichohepatoneurodevelopmental syndrome,
+BMGC_DS17367,BMG_DS066457,,,,,,,,,C4748921,,618270,MONDO:0032646,congenital anomalies of kidney and urinary tract 3,
+BMGC_DS17368,BMG_DS066458,782722002,"Global developmental delay, lung cysts, overgrowth, Wilms tumor syndrome",,,,,,,C4748924,,618272,MONDO:0018445,global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome,"Global developmental delay, lung cysts, overgrowth, Wilms tumor syndrome (disorder) | GLOW syndrome | GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumor) syndrome | Global developmental delay, lung cysts, overgrowth, Wilms tumor syndrome | GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumour) syndrome | Global developmental delay, lung cysts, overgrowth, Wilms tumour syndrome"
+BMGC_DS17369,BMG_DS066459,,MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS,,,,,DOID:0111403,mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations,C4748927,,618273;612256,MONDO:0032648,mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations,
+BMGC_DS17370,BMG_DS066460,,HYPOTRICHOSIS 14,,,,,DOID:0080582,hypotrichosis 14,C4748930,,600909;618275,MONDO:0032649,hypotrichosis 14,
+BMGC_DS17371,BMG_DS066461,,"NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY",,,,,,,C4748934,,606830;618276,MONDO:0032650,"neurodegeneration, childhood-onset, with cerebellar atrophy",
+BMGC_DS17372,BMG_DS066462,,"FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS",,,,,,,C4748939,,618278;618277,MONDO:0032651,"fibrosis, neurodegeneration, and cerebral angiomatosis",
+BMGC_DS17373,BMG_DS066463,,"CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1G",,,,,DOID:0111560,Charcot-Marie-Tooth disease type 1G,C4748940,,618279;170715,MONDO:0033135,"Charcot-Marie-Tooth disease, demyelinating, type 1G",
+BMGC_DS17374,BMG_DS066464,1332387008,Cardiac urogenital syndrome,,,,,,,C4748946,,618280,MONDO:0032653,cardiac-urogenital syndrome,Myelin regulatory factor-related cardiac urogenital syndrome | MYRF-related cardiac urogenital syndrome | Cardiac urogenital syndrome | Cardiac urogenital syndrome (disorder)
+BMGC_DS17375,BMG_DS066465,,"HYPER-IgE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE",,,,,DOID:0080595,hyper IgE recurrent infection syndrome 3,C4748969,,618282,MONDO:0032654,"hyper-IgE recurrent infection syndrome 3, autosomal recessive",
+BMGC_DS17376,BMG_DS066466,,VISUAL IMPAIRMENT AND PROGRESSIVE PHTHISIS BULBI,,,,,,,C4748978,,602678;618283,MONDO:0032655,visual impairment and progressive phthisis bulbi,
+BMGC_DS17377,BMG_DS066467,,"MICROCEPHALY, CATARACTS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSTONIA WITH ABNORMAL STRIATUM",,,,,,,C4748984,,176266;618284,MONDO:0032656,"microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum",
+BMGC_DS17378,BMG_DS066468,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 69,,,,,DOID:0112205,developmental and epileptic encephalopathy 69,C4748988,,618285;601013,MONDO:0032657,"developmental and epileptic encephalopathy, 69",
+BMGC_DS17379,BMG_DS066469,,"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT",,,,,,,C4748993,,600728;618286,MONDO:0032658,"macrocephaly, acquired, with impaired intellectual development",
+BMGC_DS17380,BMG_DS066470,,"AUTOINFLAMMATORY DISEASE, FAMILIAL, BEHCET-LIKE 3",,,,,,,C4748997,,618287,MONDO:0032659,"mucocutaneous ulceration, chronic",
+BMGC_DS17381,BMG_DS066471,,"SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT",,,,,DOID:0070350,spinal muscular atrophy with lower extremity predominant 2B,C4749003,,618291;609797,MONDO:0032660,"spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant",
+BMGC_DS17382,BMG_DS066472,,"NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA",,,,,,,C4749014,,618292;603123,MONDO:0032661,"neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia",
+BMGC_DS17383,BMG_DS066473,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 67",,,,,DOID:0081228,autosomal recessive intellectual developmental disorder 67,C4749019,,618295;603914,MONDO:0032662,"intellectual developmental disorder, autosomal recessive 67",
+BMGC_DS17384,BMG_DS066474,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 70,,,,,DOID:0112206,developmental and epileptic encephalopathy 70,C4749023,,608723;618298,MONDO:0032663,"developmental and epileptic encephalopathy, 70",
+BMGC_DS17385,BMG_DS066475,,"CILIARY DYSKINESIA, PRIMARY, 40",,,,,DOID:0111853,primary ciliary dyskinesia 40,C4749028,,618300,MONDO:0032664,"ciliary dyskinesia, primary, 40",
+BMGC_DS17386,BMG_DS066476,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68",,,,,DOID:0081229,autosomal recessive intellectual developmental disorder 68,C4749033,,611669;618302,MONDO:0032665,"intellectual developmental disorder, autosomal recessive 68",
+BMGC_DS17387,BMG_DS066477,,,,,,,,,C4749042,,618307,MONDO:0032666,"epidermodysplasia verruciformis, susceptibility to, 4",
+BMGC_DS17388,BMG_DS066478,,,,,,,,,C4749043,,618309,MONDO:0032667,"epidermodysplasia verruciformis, susceptibility to, 5",
+BMGC_DS17389,BMG_DS066483,,"PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1, DIGENIC",,,,,DOID:0050553,proteasome-associated autoinflammatory syndrome 1,C4749059,,176843;177046;256040,,,
+BMGC_DS17390,BMG_DS066508,,"MASTOCYTOSIS, CUTANEOUS AND SYSTEMIC, SOMATIC",,,,,,,C4749139,,164920,,,
+BMGC_DS17391,BMG_DS066510,,"MASTOCYTOSIS, INDOLENT",,,,,,,C4749142,,154800,,,
+BMGC_DS17392,BMG_DS066511,,MASTOCYTOSIS WITH ASSOCIATED HEMATOLOGIC DISORDER,,,,,,,C4749143,,154800,,,
+BMGC_DS17393,BMG_DS066512,,"NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL DOMINANT",,,,,,,C4749147,,605253;129010,,,
+BMGC_DS17394,BMG_DS066513,,CHROMOSOME 1p36.11 DUPLICATION SYNDROME,,,,,DOID:0070044,Coffin-Siris syndrome 2,C4749148,,614607,,,
+BMGC_DS17395,BMG_DS066514,,"PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3, DIGENIC",,,,,DOID:0060916,proteasome-associated autoinflammatory syndrome 3,C4749149,,617591,,,
+BMGC_DS17396,BMG_DS066515,,CARBOXYLESTERASE 1 DEFICIENCY,,,,,,,C4749152,,618057,,,
+BMGC_DS17397,BMG_DS066516,,CHROMOSOME 14q32 DELETION SYNDROME,,,,,,,C4749153,,618147,,,
+BMGC_DS17398,BMG_DS066540,770404004,Autosomal recessive chorioretinopathy and microcephaly syndrome,,,,,,,C4749272,,,,,"Autosomal recessive chorioretinopathy and microcephaly syndrome (disorder) | Autosomal recessive chorioretinopathy and microcephaly syndrome | Autosomal recessive chorioretinopathy, microcephaly, intellectual disability syndrome"
+BMGC_DS17399,BMG_DS066541,770405003,Benign familial mesial temporal lobe epilepsy,,,,,,,C4749273,,,,,Benign familial mesial temporal lobe epilepsy | FMTLE - familial mesial temporal lobe epilepsy | Familial mesial temporal lobe epilepsy | Familial mesial temporal lobe epilepsy (disorder)
+BMGC_DS17400,BMG_DS066542,770407006,Chuvash erythrocytosis,,,,,,,C4749274,,,,,Chuvash polycythemia | Chuvash polycythaemia | Chuvash erythrocytosis | Von Hippel Lindau dependent polycythaemia | Von Hippel Lindau dependent polycythemia | Chuvash erythrocytosis (disorder)
+BMGC_DS17401,BMG_DS066546,770431001,Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation,,,,,,,C4749281,,613971,MONDO:0017325,early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation,"Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation | Early-onset epileptic encephalopathy and intellectual disability due to glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A mutation (disorder) | Early-onset epileptic encephalopathy and intellectual disability due to glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A mutation | Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A (glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A) mutation"
+BMGC_DS17402,BMG_DS066549,,,,,,,,,C4749284,,,MONDO:0007194,familial bicuspid aortic valve,
+BMGC_DS17403,BMG_DS066556,,,,,,,,,C4749301,,607432,MONDO:0011830,lissencephaly due to LIS1 mutation,
+BMGC_DS17404,BMG_DS066558,770565003,Microcephalic primordial dwarfism Dauber type,,,,,,,C4749303,,,,,Microcephalic primordial dwarfism Dauber type | Microcephalic primordial dwarfism Dauber type (disorder)
+BMGC_DS17405,BMG_DS066559,770566002,Monosomy 13q14 syndrome,,,,,,,C4749304,,,,,Monosomy 13q14 syndrome | Monosomy 13q14 syndrome (disorder) | Deletion 13q14 | Monosomy 13q14
+BMGC_DS17406,BMG_DS066568,,"Macular Dystrophy, Retinal, 2",,,,,DOID:0070517,retinal macular dystrophy 2,C4749334,C562746,608051,MONDO:0011957,retinal macular dystrophy type 2,
+BMGC_DS17407,BMG_DS066576,770631009,Genetic transient congenital hypothyroidism,,,,,,,C4749351,,,,,Genetic transient congenital hypothyroidism (disorder) | Genetic transient congenital hypothyroidism
+BMGC_DS17408,BMG_DS066603,770687001,Vasculitis due to adenosine deaminase 2 deficiency,,,,,,,C4749403,,,,,Vasculitis due to ADA2 deficiency | Vasculitis due to adenosine deaminase 2 deficiency | Vasculitis due to adenosine deaminase 2 deficiency (disorder) | Vasculitis due to ADA2 (adenosine deaminase 2) deficiency
+BMGC_DS17409,BMG_DS066610,770721009,"Microcephaly, thin corpus callosum, intellectual disability syndrome",,,,,,,C4749429,,,,,"Microcephaly, thin corpus callosum, intellectual disability syndrome (disorder) | Microcephaly, thin corpus callosum, intellectual disability syndrome"
+BMGC_DS17410,BMG_DS066611,770722002,Proximal myopathy with extrapyramidal signs,,,,,,,C4749430,,,,,Proximal myopathy with extrapyramidal signs | Proximal myopathy with extrapyramidal signs (disorder)
+BMGC_DS17411,BMG_DS066612,770724001,Autosomal recessive spastic paraplegia type 70,,,,,,,C4749431,,,MONDO:0018422,autosomal recessive spastic paraplegia type 70,Autosomal recessive spastic paraplegia type 70 (disorder) | Autosomal recessive spastic paraplegia type 70
+BMGC_DS17412,BMG_DS066613,770725000,Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly,,,,,,,C4749432,,,,,Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly | Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly (disorder)
+BMGC_DS17413,BMG_DS066614,770726004,Female infertility due to zona pellucida defect,,,,,,,C4749433,,,,,Female infertility due to zona pellucida defect (disorder) | Female infertility due to zona pellucida defect
+BMGC_DS17414,BMG_DS066615,770727008,Spinal muscular atrophy with respiratory distress type 2,,,,,,,C4749434,,,MONDO:0018450,spinal muscular atrophy with respiratory distress type 2,SMARD2 - spinal muscular atrophy with respiratory distress type 2 | Spinal muscular atrophy with respiratory distress type 2 | Diaphragmatic spinal muscular atrophy type 2 | Severe infantile axonal neuropathy with respiratory failure type 2 | Spinal muscular atrophy with respiratory distress type 2 (disorder) | X-linked spinal muscular atrophy with respiratory distress
+BMGC_DS17415,BMG_DS066618,770751003,"Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome",,,,,,,C4749456,,,,,"Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome (disorder) | Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome"
+BMGC_DS17416,BMG_DS066619,770754006,2p21 microdeletion syndrome without cystinuria,,,,,,,C4749458,,,MONDO:0018245,2p21 microdeletion syndrome without cystinuria,2p21 microdeletion syndrome without cystinuria (disorder) | 2p21 microdeletion syndrome without cystinuria
+BMGC_DS17417,BMG_DS066620,770755007,"Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome",,,,,,,C4749459,,,,,"MCAHS (multiple congenital anomalies, hypotonia, seizures syndrome) type 3 | Congenital disorder of glycosylation due to PIGT (phosphatidylinositol glycan anchor biosynthesis class T) deficiency | Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome | Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome (disorder) | Congenital disorder of glycosylation due to PIGT deficiency"
+BMGC_DS17418,BMG_DS066623,770759001,Autosomal dominant intermediate Charcot-Marie-Tooth disease type F,,,,,,,C4749463,,615185,MONDO:0014074,Charcot-Marie-Tooth disease dominant intermediate F,Autosomal dominant intermediate Charcot-Marie-Tooth disease type F | Autosomal dominant intermediate Charcot-Marie-Tooth disease type F (disorder)
+BMGC_DS17419,BMG_DS066641,770785002,T-cell immunodeficiency with epidermodysplasia verruciformis,,,,,,,C4749500,,,MONDO:0017925,T-cell immunodeficiency with epidermodysplasia verruciformis,T-cell immunodeficiency due to RHOH (ras homolog family member H) deficiency | T-cell immunodeficiency with epidermodysplasia verruciformis | T-cell immunodeficiency due to RHOH deficiency | T-cell immunodeficiency due to ras homolog family member H deficiency | T-cell immunodeficiency due to ras homolog family member H deficiency (disorder)
+BMGC_DS17420,BMG_DS066643,770787005,Benign Samaritan congenital myopathy,,,,,,,C4749502,,,MONDO:0017936,benign Samaritan congenital myopathy,Benign Samaritan congenital myopathy (disorder) | Benign Samaritan congenital myopathy
+BMGC_DS17421,BMG_DS066644,770788000,"Tall stature, scoliosis, macrodactyly of great toe syndrome",,,,,,,C4749503,,,,,"Tall stature, scoliosis, macrodactyly of great toe syndrome | Tall stature, scoliosis, macrodactyly of great toe syndrome (disorder) | Tall stature, scoliosis, macrodactyly of hallux syndrome"
+BMGC_DS17422,BMG_DS066645,770790004,Developmental delay with autism spectrum disorder and gait instability,,,,,,,C4749505,,,,,Developmental delay with autism spectrum disorder and gait instability (disorder) | Developmental delay with autism spectrum disorder and gait instability
+BMGC_DS17423,BMG_DS066646,770792007,Adult-onset distal myopathy due to valosin containing protein mutation,,,,,,,C4749506,,,MONDO:0018006,adult-onset distal myopathy due to VCP mutation,Adult-onset distal myopathy due to VCP (valosin containing protein) mutation | Adult-onset distal myopathy due to valosin containing protein mutation (disorder) | Adult-onset distal myopathy due to VCP mutation | Adult-onset distal myopathy due to valosin containing protein mutation
+BMGC_DS17424,BMG_DS066647,770793002,5p13 microduplication syndrome,,,,,,,C4749507,,,,,5p13 microduplication syndrome (disorder) | Trisomy 5p13 | 5p13 microduplication syndrome
+BMGC_DS17425,BMG_DS066658,770896003,MITF-related melanoma and renal cell carcinoma predisposition syndrome,,,,,,,C4749577,,,,,Melanogenesis associated transcription factor related melanoma and renal cell carcinoma predisposition syndrome (disorder) | MITF-related melanoma and renal cell carcinoma predisposition syndrome | MITF (melanogenesis associated transcription factor) related melanoma and renal cell carcinoma predisposition syndrome | Melanogenesis associated transcription factor related melanoma and renal cell carcinoma predisposition syndrome
+BMGC_DS17426,BMG_DS066660,770901001,"Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome",,,,,,,C4749580,,,MONDO:0017232,recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome,"Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome (disorder) | Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome | Recessive intellectual disability, motor dysfunction, multiple joint contractures syndrome"
+BMGC_DS17427,BMG_DS066661,770902008,Distal monosomy 12p,,,,,,,C4749581,,,MONDO:0017229,distal monosomy 12p,Distal monosomy 12p | Distal deletion 12p | Distal monosomy 12p (disorder) | 12p13.33 microdeletion syndrome
+BMGC_DS17428,BMG_DS066675,770947009,Autosomal dominant severe congenital neutropenia,,,,,,,C4749612,,,MONDO:0008742,autosomal dominant severe congenital neutropenia,Autosomal dominant severe congenital neutropaenia | Autosomal dominant severe congenital neutropenia (disorder) | Autosomal dominant severe congenital neutropenia
+BMGC_DS17429,BMG_DS066677,771074000,"Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome",,,,,,,C4749647,,,MONDO:0018494,microcephaly-short stature-intellectual disability-facial dysmorphism syndrome,"Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome (disorder) | Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome"
+BMGC_DS17430,BMG_DS066681,771078002,Immunodeficiency due to MASP-2 deficiency,,,,,,,C4749651,,,,,Immunodeficiency due to MASP-2 (mannan binding lectin serine peptidase 2) deficiency | Immunodeficiency due to MASP-2 deficiency | Immunodeficiency due to mannan binding lectin serine peptidase 2 deficiency (disorder) | Immunodeficiency due to mannan binding lectin serine peptidase 2 deficiency
+BMGC_DS17431,BMG_DS066682,,,,,,,,,C4749652,,,MONDO:0016249,hereditary site-specific ovarian cancer syndrome,
+BMGC_DS17432,BMG_DS066683,771081007,Distal hereditary motor neuropathy type 7,,,,,,,C4749653,,,MONDO:0015355,distal hereditary motor neuropathy type 7,Distal hereditary motor neuropathy type 7 | Distal spinal muscular atrophy with vocal cord paralysis | Distal hereditary motor neuropathy type 7 (disorder)
+BMGC_DS17433,BMG_DS066706,771306007,"Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome",,,,,,,C4749823,,,,,"POIKTMP syndrome | Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome (disorder) | POIKTMP (poikiloderma, tendon contractures, myopathy, pulmonary fibrosis) syndrome | Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome"
+BMGC_DS17434,BMG_DS066707,771307003,Charcot-Marie-Tooth disease type 2B5,,,,,,,C4749824,,,MONDO:0016454,Charcot-Marie-Tooth disease type 2B5,Severe early-onset axonal neuropathy due to NEFL (neurofilament light) deficiency | Severe early-onset axonal neuropathy due to NEFL deficiency | Severe early-onset axonal neuropathy due to light neurofilament subunit deficiency | Autosomal recessive Charcot-Marie-Tooth disease type 2B5 | Charcot-Marie-Tooth disease type 2B5 | Charcot-Marie-Tooth disease type 2B5 (disorder)
+BMGC_DS17435,BMG_DS066708,771308008,"Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome",,,,,,,C4749825,,,,,"Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome (disorder) | Non-acquired combined pituitary hormone deficiency, deafness, rigid cervical spine syndrome | Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome"
+BMGC_DS17436,BMG_DS066710,771333006,"Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome",,,,,,,C4749850,,,MONDO:0016542,immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome,"IL10-related early-onset inflammatory bowel disease | Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome | Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome (disorder) | Interleukin 10 related early-onset inflammatory bowel disease | IL10 (interleukin 10) related early-onset inflammatory bowel disease"
+BMGC_DS17437,BMG_DS066711,771335004,Ectodermal dysplasia syndactyly syndrome,,,,,,,C4749852,,,MONDO:0013311,ectodermal dysplasia-syndactyly syndrome,Ectodermal dysplasia syndactyly syndrome (disorder) | Ectodermal dysplasia syndactyly syndrome
+BMGC_DS17438,BMG_DS066713,771340007,15q11.2 microdeletion syndrome,,,,,,,C4749854,,,,,Monosomy 15q11.2 | 15q11.2 microdeletion syndrome | 15q11.2 microdeletion syndrome (disorder)
+BMGC_DS17439,BMG_DS066714,771341006,14q11.2 microduplication syndrome,,,,,,,C4749855,,,MONDO:0016835,14q11.2 microduplication syndrome,14q11.2 microduplication syndrome (disorder) | 14q11.2 microduplication syndrome | Trisomy 14q11.2
+BMGC_DS17440,BMG_DS066715,771342004,"Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome",,,,,,,C4749856,,,MONDO:0016979,MRCS syndrome,"Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder) | Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome | MRCS syndrome | MRCS (microcornea, rod-cone dystrophy, cataract, posterior staphyloma) syndrome"
+BMGC_DS17441,BMG_DS066717,771444002,Methylmalonic aciduria due to transcobalamin receptor defect,,,,,,,C4749905,,613646,MONDO:0013341,methylmalonic acidemia due to transcobalamin receptor defect,Methylmalonic aciduria due to transcobalamin receptor defect (disorder) | Methylmalonic acidaemia TCb1R type | Methylmalonic aciduria due to transcobalamin receptor defect | Methylmalonic acidemia TCb1R type
+BMGC_DS17442,BMG_DS066720,771448004,Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency,,,,,,,C4749908,,,,,Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency (disorder) | Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency
+BMGC_DS17443,BMG_DS066721,771471002,"Optic nerve edema, splenomegaly syndrome",,,,,,,C4749914,,614979,MONDO:0013999,"retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis, and migraine headache syndrome","Optic nerve edema, splenomegaly syndrome (disorder) | Optic nerve oedema, splenomegaly syndrome | Optic nerve edema, splenomegaly syndrome"
+BMGC_DS17444,BMG_DS066722,771472009,Developmental and speech delay due to SOX5 deficiency,,,,,,,C4749915,,,MONDO:0017782,developmental and speech delay due to SOX5 deficiency,Developmental and speech delay due to SRY-box 5 deficiency | Developmental and speech delay due to SOX5 (SRY-box 5) deficiency | Developmental and speech delay due to SRY-box 5 deficiency (disorder) | Developmental and speech delay due to SOX5 deficiency
+BMGC_DS17445,BMG_DS066724,,,,,,,,,C4749917,,619182,MONDO:0017790,gastric adenocarcinoma and proximal polyposis of the stomach,
+BMGC_DS17446,BMG_DS066725,771475006,Young adult-onset distal hereditary motor neuropathy,,,,,,,C4749918,,614881,MONDO:0013947,"neuronopathy, distal hereditary motor, autosomal recessive 5",Young adult-onset distal hereditary motor neuropathy | Autosomal recessive distal spinal muscular atrophy type 5 | Young adult-onset distal hereditary motor neuropathy (disorder)
+BMGC_DS17447,BMG_DS066728,771478008,Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency,,,,,,,C4749921,,614702,MONDO:0013865,mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency,COXPD10 - combined oxidative phosphorylation defect type 10 | Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency | Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimisation 1 deficiency | Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimization 1 deficiency (disorder) | Combined oxidative phosphorylation defect type 10 | Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimization 1 deficiency
+BMGC_DS17448,BMG_DS066729,771479000,Combined immunodeficiency due to STK4 deficiency,,,,,,,C4749922,,,,,Combined immunodeficiency due to STK4 deficiency | Combined immunodeficiency due to serine/threonine kinase 4 deficiency (disorder) | Combined immunodeficiency due to serine/threonine kinase 4 deficiency | Combined immunodeficiency due to STK4 (serine/threonine kinase 4) deficiency
+BMGC_DS17449,BMG_DS066732,771510006,X-linked central congenital hypothyroidism with late-onset testicular enlargement,,,,,,,C4749943,,,,,X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) | IGSF1 (immunoglobulin superfamily member 1) deficiency syndrome | X-linked central congenital hypothyroidism with late-onset macroorchidism | X-linked central congenital hypothyroidism with late-onset testicular enlargement
+BMGC_DS17450,BMG_DS066733,771511005,Thrombocythemia with distal limb defect,,,,,,,C4749944,,,MONDO:0018000,hereditary thrombocytosis with transverse limb defect,Familial thrombocytosis with transverse limb defect | Thrombocythemia with distal limb defect (disorder) | Thrombocythemia with distal limb defect | Hereditary thrombocytosis with transverse limb defect | Thrombocythaemia with distal limb defect
+BMGC_DS17451,BMG_DS066734,771512003,Autism spectrum disorder due to AUTS2 deficiency,,,,,,,C4749945,,,,,Autism spectrum disorder due to AUTS2 activator of transcription and developmental regulator deficiency | Autism spectrum disorder due to AUTS2 deficiency | Autism spectrum disorder due to AUTS2 activator of transcription and developmental regulator deficiency (disorder) | AUTS2 syndrome
+BMGC_DS17452,BMG_DS066735,771513008,Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency,,,,,,,C4749946,,,,,Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency (disorder) | Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency | Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency | Combined oxidative phosphorylation defect type 16
+BMGC_DS17453,BMG_DS066736,771514002,"Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome",,,,,,,C4749947,,,,,"Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) | Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome"
+BMGC_DS17454,BMG_DS066737,771515001,"Facial dysmorphism, immunodeficiency, livedo, short stature syndrome",,,,,,,C4749948,,,,,"FILS syndrome | Facial dysmorphism, immunodeficiency, livedo, short stature syndrome | Facial dysmorphism, immunodeficiency, livedo, short stature syndrome (disorder) | FILS (facial dysmorphism, immunodeficiency, livedo, short stature) syndrome"
+BMGC_DS17455,BMG_DS066738,771517009,Severe combined immunodeficiency due to CARD11 deficiency,,,,,,,C4749949,,,,,Severe combined immunodeficiency due to CARD11 deficiency | Severe combined immunodeficiency due to caspase recruitment domain family member 11 deficiency | Severe combined immunodeficiency due to CARD11 (caspase recruitment domain family member 11) deficiency | Severe combined immunodeficiency due to caspase recruitment domain family member 11 deficiency (disorder)
+BMGC_DS17456,BMG_DS066874,773230003,Cyclin-dependent kinase-like 5 deficiency,,,,,,,C4750718,,300672,MONDO:0010396,"developmental and epileptic encephalopathy, 2",Cyclin-dependent kinase-like 5 deficiency (disorder) | CDKL5 (cyclin-dependent kinase-like 5) deficiency | CDKL5 deficiency disorder | Cyclin-dependent kinase-like 5 deficiency | CDKL5-related epileptic encephalopathy
+BMGC_DS17457,BMG_DS066904,773305003,"Microcephaly, polymicrogyria, corpus callosum agenesis syndrome",,,,,,,C4750772,,,MONDO:0015745,microcephaly-polymicrogyria-corpus callosum agenesis syndrome,"Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | Microcephaly, polymicrogyria, corpus callosum agenesis syndrome"
+BMGC_DS17458,BMG_DS066905,773306002,Congenital lethal myopathy Compton North type,,,,,,,C4750773,,,,,Congenital lethal myopathy Compton North type | Congenital lethal myopathy Compton North type (disorder)
+BMGC_DS17459,BMG_DS066906,773308001,Autosomal recessive intermediate Charcot-Marie-Tooth disease type A,,,,,,,C4750774,,,,,Autosomal recessive intermediate Charcot-Marie-Tooth disease type A | Autosomal recessive intermediate Charcot-Marie-Tooth disease type A (disorder) | RI-CMT (recessive intermediate Charcot-Marie-Tooth) type A
+BMGC_DS17460,BMG_DS066909,773326003,7q31 microdeletion syndrome,,,,,,,C4750783,,,MONDO:0016656,7q31 microdeletion syndrome,Monosomy 7q31 | 7q31 microdeletion syndrome (disorder) | 7q31 microdeletion syndrome
+BMGC_DS17461,BMG_DS066911,773330000,Autosomal recessive intermediate Charcot-Marie-Tooth disease type B,,,,,,,C4750786,,,,,Autosomal recessive intermediate Charcot-Marie-Tooth disease type B (disorder) | Autosomal recessive intermediate Charcot-Marie-Tooth disease type B | RI-CMT (recessive intermediate Charcot-Marie-Tooth) type B
+BMGC_DS17462,BMG_DS066912,773333003,Autosomal systemic lupus erythematosus,,,,,,,C4750787,,,,,Autosomal systemic lupus erythematosus (disorder) | Autosomal systemic lupus erythematosus | Autosomal SLE (systemic lupus erythematosus) | Familial systemic lupus erythematosus
+BMGC_DS17463,BMG_DS066913,773345007,Oligodontia and cancer predisposition syndrome,,,,,,,C4750788,,,,,Oligodontia and cancer predisposition syndrome | Oligodontia and cancer predisposition syndrome (disorder)
+BMGC_DS17464,BMG_DS066917,773398005,"Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome",,,,,,,C4750835,,,,,"Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome | Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome (disorder) | Congenital cataract, progressive muscular hypotonia, deafness, developmental delay syndrome"
+BMGC_DS17465,BMG_DS066919,,Bainbridge-Ropers syndrome,,,,,,,C4750837,C000726367,615485,MONDO:0014205,severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome,
+BMGC_DS17466,BMG_DS066920,773405004,Intellectual disability with strabismus syndrome,,,,,,,C4750838,,615286,MONDO:0014119,intellectual disability-strabismus syndrome,Intellectual disability with strabismus syndrome (disorder) | Intellectual disability with strabismus syndrome
+BMGC_DS17467,BMG_DS066922,773414009,Autosomal recessive intermediate Charcot-Marie-Tooth disease type C,,,,,,,C4750846,,,,,Autosomal recessive intermediate Charcot-Marie-Tooth disease type C (disorder) | Autosomal recessive intermediate Charcot-Marie-Tooth disease type C | RI-CMT (recessive intermediate Charcot-Marie-Tooth) type C
+BMGC_DS17468,BMG_DS066924,773418007,XYLT1-CDG - xylosyltransferase 1 congenital disorder of glycosylation,,,,,,,C4750849,,,MONDO:0018273,XYLT1-congenital disorder of glycosylation,Xylosyltransferase 1 congenital disorder of glycosylation | XYLT1-CDG - xylosyltransferase 1 congenital disorder of glycosylation | Xylosyltransferase 1 congenital disorder of glycosylation (disorder) | XYLT1-CDG
+BMGC_DS17469,BMG_DS066926,773419004,"Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome",,,,,,,C4750851,,,,,"Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome (disorder) | Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome"
+BMGC_DS17470,BMG_DS066928,773421009,Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression,,,,,,,C4750853,,,MONDO:0018314,infantile-onset mesial temporal lobe epilepsy with severe cognitive regression,Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression (disorder) | Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
+BMGC_DS17471,BMG_DS066929,773422002,East Texas bleeding disorder,,,,,,,C4750854,,,,,East Texas bleeding disorder (disorder) | East Texas bleeding disorder
+BMGC_DS17472,BMG_DS066930,773423007,Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency,,,,,,,C4750855,,,,,Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency (disorder) | Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency
+BMGC_DS17473,BMG_DS066932,773425000,Autosomal recessive spastic paraplegia type 59,,,,,,,C4750857,,,MONDO:0018416,autosomal recessive spastic paraplegia type 59,Autosomal recessive spastic paraplegia type 59 | Autosomal recessive spastic paraplegia type 59 (disorder)
+BMGC_DS17474,BMG_DS066933,773426004,LMNA-related cardiocutaneous progeria syndrome,,,,,,,C4750858,,,MONDO:0018203,LMNA-related cardiocutaneous progeria syndrome,Lamin A/C related cardiocutaneous progeria syndrome | LMNA-related cardiocutaneous progeria syndrome | Lamin A/C related cardiocutaneous progeria syndrome (disorder)
+BMGC_DS17475,BMG_DS066943,773488000,Combined immunodeficiency due to MALT1 deficiency,,,,,,,C4750906,,,,,Combined immunodeficiency due to mucosa-associated lymphoid tissue lymphoma translocation gene 1 deficiency (disorder) | Combined immunodeficiency due to mucosa-associated lymphoid tissue lymphoma translocation gene 1 deficiency | Combined immunodeficiency due to MALT1 deficiency
+BMGC_DS17476,BMG_DS066944,773489008,Hereditary cryohydrocytosis with normal stomatin,,,,,,,C4750907,,,,,Hereditary cryohydrocytosis with normal stomatin (disorder) | Hereditary cryohydrocytosis with normal stomatin
+BMGC_DS17477,BMG_DS066950,773497001,"Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome",,,,,,,C4750913,,,MONDO:0018430,partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome,"Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome | Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome (disorder)"
+BMGC_DS17478,BMG_DS066951,773498006,"Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency",,,,,,,C4750914,,616949,MONDO:0014846,"spinocerebellar ataxia, autosomal recessive 23","Spinocerebellar ataxia autosomal recessive type 23 | SCAR23 - spinocerebellar ataxia autosomal recessive type 23 | Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (disorder) | Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency"
+BMGC_DS17479,BMG_DS066954,773501006,Epidermolysis bullosa simplex due to BP230 deficiency,,,,,,,C4750917,,,,,Epidermolysis bullosa simplex due to BP230 deficiency (disorder) | Epidermolysis bullosa simplex due to BP230 deficiency | DST (dystonin) related epidermolysis bullosa simplex
+BMGC_DS17480,BMG_DS066955,773503009,Epidermolysis bullosa simplex due to exophilin 5 deficiency,,,,,,,C4750918,,,,,Epidermolysis bullosa simplex due to exophilin 5 deficiency (disorder) | Epidermolysis bullosa simplex due to exophilin 5 deficiency
+BMGC_DS17481,BMG_DS066965,773548008,"Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome",,,,,,,C4750952,,,,,"Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome (disorder) | Epilepsy, cortical blindness, intellectual disability, facial dysmorphism syndrome | Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome"
+BMGC_DS17482,BMG_DS066966,773549000,Maternal riboflavin deficiency,,,,,,,C4750953,,,MONDO:0014013,maternal riboflavin deficiency,Maternal riboflavin deficiency | Maternal riboflavin deficiency (disorder)
+BMGC_DS17483,BMG_DS066967,773551001,"Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome",,,,,,,C4750954,,,,,"Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome (disorder) | Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome"
+BMGC_DS17484,BMG_DS066968,773552008,"Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome",,,,,,,C4750955,,,,,"Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome | Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome (disorder)"
+BMGC_DS17485,BMG_DS066969,773555005,Severe neurodegenerative syndrome with lipodystrophy,,,,,,,C4750956,,,,,"Severe neurodegenerative syndrome due to BSCL2 deficiency | Severe neurodegenerative syndrome due to BSCL2, seipin lipid droplet biogenesis associated deficiency | Severe neurodegenerative syndrome with lipodystrophy | Severe neurodegenerative syndrome with lipodystrophy (disorder)"
+BMGC_DS17486,BMG_DS066974,773576000,Progressive retinal dystrophy due to retinol transport defect,,,,,,,C4751000,,,,,"Retinol dystrophy, iris coloboma, comedogenic acne syndrome | Progressive retinal dystrophy due to retinol transport defect (disorder) | Progressive retinal dystrophy due to retinol transport defect"
+BMGC_DS17487,BMG_DS066975,773577009,"Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome",,,,,,,C4751001,,,,,"Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome | Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome (disorder)"
+BMGC_DS17488,BMG_DS066977,773579007,Congenital chronic diarrhea with protein-losing enteropathy,,,,,,,C4751003,,,,,Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Congenital chronic diarrhea with exudative enteropathy | Congenital chronic diarrhoea with protein-losing enteropathy | Congenital chronic diarrhea with protein-losing enteropathy | Congenital chronic diarrhoea with exudative enteropathy
+BMGC_DS17489,BMG_DS066980,773587008,"X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome",,,,,,,C4751008,,,,,"X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome (disorder) | X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome"
+BMGC_DS17490,BMG_DS067000,773627004,"Porencephaly, microcephaly, bilateral congenital cataract syndrome",,,,,,,C4751076,,,,,"Porencephaly, microcephaly, bilateral congenital cataract syndrome (disorder) | Porencephaly, microcephaly, bilateral congenital cataract syndrome"
+BMGC_DS17491,BMG_DS067001,773628009,"Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome",,,,,,,C4751077,,,,,"Frontonasal dysplasia type 3 | ALX1-related frontonasal dysplasia | Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome (disorder) | ALX1 (aristaless-like homeobox 1) related frontonasal dysplasia | Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome"
+BMGC_DS17492,BMG_DS067013,773643006,"Multiple congenital anomalies, hypotonia, seizures syndrome type 2",,,,,,,C4751110,,,,,"Multiple congenital anomalies, hypotonia, seizures syndrome type 2 | MCAHS (multiple congenital anomalies, hypotonia, seizures syndrome) type 2 | Multiple congenital anomalies, hypotonia, seizures syndrome type 2 (disorder)"
+BMGC_DS17493,BMG_DS067014,773644000,"Progeroid and marfanoid aspect, lipodystrophy syndrome",,,,,,,C4751111,,,,,"Progeroid and marfanoid aspect, lipodystrophy syndrome (disorder) | Progeroid and marfanoid aspect, lipodystrophy syndrome"
+BMGC_DS17494,BMG_DS067016,773647007,"Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome",,,,,,,C4751113,,,,,"Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome (disorder) | Nephrotic syndrome, hearing loss, pretibial epidermolysis bullosa syndrome"
+BMGC_DS17495,BMG_DS067017,773648002,"Congenital cataract, hearing loss, severe developmental delay syndrome",,,,,,,C4751114,,614482,MONDO:0013772,Huppke-Brendel syndrome,"Congenital cataract, hearing loss, severe developmental delay syndrome (disorder) | Congenital cataract, hearing loss, severe developmental delay syndrome | Congenital cataract, deafness, severe developmental delay syndrome | Lethal neurodegenerative disorder due to copper transport defect"
+BMGC_DS17496,BMG_DS067018,773649005,Transient infantile hypertriglyceridemia and hepatosteatosis,,,,,,,C4751115,,,,,Transient infantile hypertriglyceridemia and hepatosteatosis | Transient infantile hypertriglyceridemia and fatty liver | Transient infantile hypertriglyceridemia and hepatosteatosis (disorder) | Transient infantile hypertriglyceridaemia and hepatosteatosis | Transient infantile hypertriglyceridaemia and fatty liver
+BMGC_DS17497,BMG_DS067019,773662009,Neonatal inflammatory skin and bowel disease,,,,,,,C4751120,,,MONDO:0017411,neonatal inflammatory skin and bowel disease,Neonatal inflammatory skin and bowel disease (disorder) | Neonatal inflammatory skin and bowel disease
+BMGC_DS17498,BMG_DS067021,773664005,"Deficiency in anterior pituitary function, variable immunodeficiency syndrome",,,,,,,C4751122,,,MONDO:0017407,deficiency in anterior pituitary function - variable immunodeficiency syndrome,"Deficiency in anterior pituitary function, variable immunodeficiency syndrome (disorder) | Deficiency in anterior pituitary function, variable immunodeficiency syndrome | DAVID (deficiency in anterior pituitary function, variable immunodeficiency) syndrome"
+BMGC_DS17499,BMG_DS067023,773666007,Hypoinsulinemic hypoglycemia and body hemihypertrophy,,,,,,,C4751124,,,,,Hypoinsulinemic hypoglycemia and body hemihypertrophy | Hypoinsulinemic hypoglycemia and body hemihypertrophy (disorder) | Hypoinsulinemic hypoglycaemia and body hemihypertrophy
+BMGC_DS17500,BMG_DS067024,773667003,"Hypertelorism, preauricular sinus, punctual pits, deafness syndrome",,,,,,,C4751125,,614187,MONDO:0013614,hypertelorism-preauricular sinus-punctual pits-deafness syndrome,"Hypertelorism, preauricular sinus, punctual pits, deafness syndrome (disorder) | Hypertelorism, preauricular sinus, punctual pits, deafness syndrome | HPPD (hypertelorism, preauricular sinus, punctual pits, deafness) syndrome | Hypertelorism, preauricular sinus, punctual pits, hearing loss syndrome"
+BMGC_DS17501,BMG_DS067026,773672007,"Lethal occipital encephalocele, skeletal dysplasia syndrome",,,,,,,C4751129,,,,,"Lethal occipital encephalocele, skeletal dysplasia syndrome (disorder) | Lethal occipital encephalocele, skeletal dysplasia syndrome"
+BMGC_DS17502,BMG_DS067027,773673002,"Hypoplasia of pancreas, intestinal atresia, hypoplasia of gallbladder syndrome",,,,,,,C4751130,,,,,"Hypoplasia of pancreas, intestinal atresia, hypoplasia of gallbladder syndrome (disorder) | Hypoplastic pancreas, intestinal atresia, hypoplastic gallbladder syndrome | Hypoplasia of pancreas, intestinal atresia, hypoplasia of gallbladder syndrome"
+BMGC_DS17503,BMG_DS067028,773668008,Childhood encephalopathy due to thiamine pyrophosphokinase deficiency,,,,,,,C4751138,,,,,Childhood encephalopathy due to thiamine pyrophosphokinase deficiency (disorder) | Childhood encephalopathy due to thiamine pyrophosphokinase deficiency | Childhood encephalopathy due to thiamin pyrophosphokinase deficiency
+BMGC_DS17504,BMG_DS067052,,,,,,,,,C4751168,,,MONDO:0016377,Pitt-Hopkins-like syndrome,
+BMGC_DS17505,BMG_DS067060,773726000,Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency,,,,,,,C4751204,,,MONDO:0016203,hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency,Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency | Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency (disorder) | Hypercholesterolaemia due to cholesterol 7alpha-hydroxylase deficiency
+BMGC_DS17506,BMG_DS067061,773730002,Osteopetrosis hypogammaglobulinemia syndrome,,,,,,,C4751205,,,,,Autosomal recessive osteopetrosis type 7 | Osteopetrosis hypogammaglobulinemia syndrome (disorder) | Autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia | Autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinaemia | Osteopetrosis hypogammaglobulinemia syndrome | Osteopetrosis hypogammaglobulinaemia syndrome
+BMGC_DS17507,BMG_DS067072,773771008,Rare isolated myopia,,,,,,,C4751232,,,,,Rare isolated myopia | Rare isolated myopia (disorder)
+BMGC_DS17508,BMG_DS067104,,,,,,,,,C4751434,,,MONDO:0016103,isolated asymptomatic elevation of creatine phosphokinase,
+BMGC_DS17509,BMG_DS067111,774069007,PRKAR1B-related neurodegenerative dementia with intermediate filaments,,,,,,,C4751505,,,MONDO:0018475,PRKAR1B-related neurodegenerative dementia with intermediate filaments,Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments | PRKAR1B-related neurodegenerative dementia with intermediate filaments | Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments (disorder)
+BMGC_DS17510,BMG_DS067112,774070008,"FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome",,,,,,,C4751506,,,MONDO:0018443,FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome,"FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome | Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome (disorder) | Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome"
+BMGC_DS17511,BMG_DS067113,774071007,Pancytopenia with developmental delay syndrome,,,,,,,C4751507,,,,,Trilineage bone marrow failure with developmental delay syndrome | Pancytopenia with developmental delay syndrome | Pancytopenia with developmental delay syndrome (disorder)
+BMGC_DS17512,BMG_DS067127,774150004,"Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome",,,,,,,C4751569,,,,,"Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome | Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder)"
+BMGC_DS17513,BMG_DS067128,774151000,Ferro-cerebro-cutaneous syndrome,,,,,,,C4751570,,301072,MONDO:0018346,ferro-cerebro-cutaneous syndrome,Cerebro-cutaneous syndrome with iron overload | Ferro-cerebro-cutaneous syndrome | Ferro-cerebro-cutaneous syndrome (disorder)
+BMGC_DS17514,BMG_DS067129,774152007,Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies,,,,,,,C4751571,,,,,Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies | Retinal dystrophy with inner nuclear layer and ganglion cell anomalies | Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies (disorder)
+BMGC_DS17515,BMG_DS067130,774153002,Periodic paralysis with transient compartment-like syndrome,,,,,,,C4751572,,,,,Periodic paralysis with transient compartment-like syndrome (disorder) | Periodic paralysis with transient compartment-like syndrome
+BMGC_DS17516,BMG_DS067131,774154008,Periodic paralysis with later-onset distal motor neuropathy,,,,,,,C4751573,,,MONDO:0018343,periodic paralysis with later-onset distal motor neuropathy,Periodic paralysis with later-onset distal motor neuropathy (disorder) | Periodic paralysis with later-onset distal motor neuropathy
+BMGC_DS17517,BMG_DS067132,774155009,"Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome",,,,,,,C4751574,,,,,"Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome | Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome (disorder) | SAMS syndrome | SAMS (short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies) syndrome"
+BMGC_DS17518,BMG_DS067133,774203000,"Intellectual disability, severe speech delay, mild dysmorphism syndrome",,,,,,,C4751594,,,,,"Intellectual disability, severe speech delay, mild dysmorphism syndrome (disorder) | Intellectual disability, severe speech delay, mild dysmorphism syndrome"
+BMGC_DS17519,BMG_DS067134,774204006,"Growth retardation, mild developmental delay, chronic hepatitis syndrome",,,,,,,C4751595,,,MONDO:0018317,growth retardation-mild developmental delay-chronic hepatitis syndrome,"Growth retardation, mild developmental delay, chronic hepatitis syndrome | Growth retardation, mild developmental delay, chronic hepatitis syndrome (disorder)"
+BMGC_DS17520,BMG_DS067135,774205007,"Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome",,,,,,,C4751596,,,,,"Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome | Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome (disorder)"
+BMGC_DS17521,BMG_DS067136,774206008,Fatal post-viral neurodegenerative disorder,,,,,,,C4751597,,,MONDO:0018316,fatal post-viral neurodegenerative disorder,Fatal post-viral neurodegenerative disorder | Fatal post-viral neurodegenerative disorder (disorder)
+BMGC_DS17522,BMG_DS067137,774207004,Acute infantile liver failure with multisystemic involvement syndrome,,,,,,,C4751598,,,,,Acute infantile liver failure with multisystemic involvement syndrome | Acute infantile liver failure with multisystemic involvement syndrome (disorder)
+BMGC_DS17523,BMG_DS067141,774212003,"Microcornea, myopic chorioretinal atrophy, telecanthus syndrome",,,,,,,C4751602,,,,,"Microcornea, myopic chorioretinal atrophy, telecanthus syndrome (disorder) | MMCAT syndrome | MMCAT (microcornea, myopic chorioretinal atrophy, telecanthus) syndrome | Microcornea, myopic chorioretinal atrophy, telecanthus syndrome"
+BMGC_DS17524,BMG_DS067143,775909002,"Congenital neutropenia, myelofibrosis, nephromegaly syndrome",,,,,,,C4755251,,,,,"Congenital neutropenia, myelofibrosis, nephromegaly syndrome (disorder) | Congenital neutropenia, bone marrow fibrosis, nephromegaly syndrome | VPS45 deficiency | Congenital neutropenia, myelofibrosis, nephromegaly syndrome"
+BMGC_DS17525,BMG_DS067144,776087007,Autosomal recessive cerebral atrophy,,,,,,,C4755252,,,MONDO:0018218,autosomal recessive cerebral atrophy,Autosomal recessive cerebral atrophy | Autosomal recessive cerebral atrophy (disorder)
+BMGC_DS17526,BMG_DS067146,777999008,Hypomyelination with brain stem and spinal cord involvement and leg spasticity,,,,,,,C4755254,,615281,MONDO:0014115,hypomyelination with brain stem and spinal cord involvement and leg spasticity,"HBSL - hypomyelination, brain stem, spinal cord, leg spasticity | Hypomyelination with brain stem and spinal cord involvement and leg spasticity (disorder) | Hypomyelination with brain stem and spinal cord involvement and leg spasticity"
+BMGC_DS17527,BMG_DS067148,778001003,KCNQ2-related epileptic encephalopathy,,,,,,,C4755256,,,,,Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy (disorder) | KCNQ2-related neonatal epileptic encephalopathy | KCNQ2-NEE - potassium voltage-gated channel subfamily Q member 2-related neonatal epileptic encephalopathy | KCNQ2-related epileptic encephalopathy | Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy
+BMGC_DS17528,BMG_DS067149,778003000,Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain,,,,,,,C4755257,,,MONDO:0017937,autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain,Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain | Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain (disorder)
+BMGC_DS17529,BMG_DS067151,778006008,Autosomal dominant aplasia and myelodysplasia,,,,,,,C4755259,,,,,Autosomal dominant aplasia and myelodysplasia (disorder) | Autosomal dominant aplasia and myelodysplasia | Autosomal dominant aplastic anaemia and myelodysplasia | Autosomal dominant aplastic anemia and myelodysplasia
+BMGC_DS17530,BMG_DS067152,778007004,12p12.1 microdeletion syndrome,,,,,,,C4755260,,,MONDO:0017781,12p12.1 microdeletion syndrome,12p12.1 microdeletion syndrome | Monosomy 12p12.1 | 12p12.1 microdeletion syndrome (disorder)
+BMGC_DS17531,BMG_DS067153,778008009,FGFR2-related bent bone dysplasia,,,,,,,C4755261,,,,,Perinatal lethal bent bone dysplasia | Fibroblast growth factor receptor 2-related bent bone dysplasia (disorder) | Fibroblast growth factor receptor 2-related bent bone dysplasia | FGFR2-related bent bone dysplasia
+BMGC_DS17532,BMG_DS067155,778010006,"Skin fragility, wooly hair, palmoplantar keratoderma syndrome",,,,,,,C4755263,,607655,MONDO:0011882,skin fragility-woolly hair-palmoplantar keratoderma syndrome,"Skin fragility, wooly hair, palmoplantar keratoderma syndrome (disorder) | Skin fragillity, woolly hair, palmoplantar keratoderma syndrome | Skin fragility, wooly hair, palmoplantar keratoderma syndrome"
+BMGC_DS17533,BMG_DS067156,778011005,Severe intellectual disability and progressive spastic paraplegia,,,,,,,C4755264,,,,,Severe intellectual disability and progressive spastic paraplegia | Severe intellectual disability and progressive spastic paraplegia (disorder) | AP4 deficiency syndrome
+BMGC_DS17534,BMG_DS067160,778021002,"Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome",,,,,,,C4755272,,,,,"Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome (disorder) | Nanophthalmos, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome"
+BMGC_DS17535,BMG_DS067161,778023004,Syndromic multisystem autoimmune disease due to ITCH deficiency,,,,,,,C4755273,,,,,Syndromic multisystem autoimmune disease due to itchy E3 ubiquitin protein ligase deficiency (disorder) | Syndromic multisystem autoimmune disease due to ITCH deficiency | Syndromic multisystem autoimmune disease due to itchy E3 ubiquitin protein ligase deficiency
+BMGC_DS17536,BMG_DS067162,778025006,Atypical hypotonia cystinuria syndrome,,,,,,,C4755274,,,MONDO:0016539,atypical hypotonia-cystinuria syndrome,Atypical hypotonia cystinuria syndrome (disorder) | Atypical hypotonia cystinuria syndrome
+BMGC_DS17537,BMG_DS067163,778026007,Lethal polymalformative syndrome Boissel type,,,,,,,C4755275,,,,,Lethal polymalformative syndrome Boissel type | Lethal polymalformative syndrome Boissel type (disorder)
+BMGC_DS17538,BMG_DS067164,778027003,Primary CD59 deficiency,,,,,,,C4755276,,,,,Primary CD59 deficiency | Primary CD59 deficiency (disorder)
+BMGC_DS17539,BMG_DS067165,778028008,Immunodeficiency due to CD25 deficiency,,,,,,,C4755277,,,,,Interleukin-2 receptor alpha chain deficiency | Immunodeficiency due to CD25 deficiency (disorder) | Immunodeficiency due to CD25 deficiency
+BMGC_DS17540,BMG_DS067166,778029000,FASTKD2-related infantile mitochondrial encephalomyopathy,,,,,,,C4755278,,,MONDO:0015632,FASTKD2-related infantile mitochondrial encephalomyopathy,FAST kinase domains 2-related infantile mitochondrial encephalomyopathy (disorder) | FAST kinase domains 2-related infantile mitochondrial encephalomyopathy | FASTKD2-related infantile mitochondrial encephalomyopathy
+BMGC_DS17541,BMG_DS067174,778045003,Susceptibility to viral and mycobacterial infection,,,,,,,C4755296,,,,,Signal transducer and activator of transcription 1 deficiency | STAT1 deficiency | Susceptibility to viral and mycobacterial infection | Susceptibility to viral and mycobacterial infection (disorder)
+BMGC_DS17542,BMG_DS067177,778048001,MT-ATP6-related mitochondrial spastic paraplegia,,,,,,,C4755299,,,MONDO:0017917,maternally-inherited spastic paraplegia,Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia | Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia (disorder) | Maternally-inherited spastic paraplegia | MT-ATP6-related mitochondrial spastic paraplegia
+BMGC_DS17543,BMG_DS067180,778051008,Focal palmoplantar keratoderma with joint keratoses,,,,,,,C4755302,,,MONDO:0018252,focal palmoplantar keratoderma with joint keratoses,Focal palmoplantar keratoderma with joint keratoses (disorder) | Focal palmoplantar keratoderma with joint keratoses
+BMGC_DS17544,BMG_DS067181,778060000,COL4A1-related familial vascular leukoencephalopathy,,,,,,,C4755307,,,,,"Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy (disorder) | COL4A1-related familial vascular leukoencephalopathy | Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy | COL4A1-related retinal arteriolar tortuosity, infantile hemiparesis, autosomal dominant leukoencephalopathy syndrome | COL4A1-related brain small vessel disease with hemorrhage | COL4A1-related brain small vessel disease with haemorrhage | COL4A1-related familial vascular leucoencephalopathy | Collagen type IV alpha 1 chain related familial vascular leucoencephalopathy | COL4A1-related retinal arteriolar tortuosity, infantile hemiparesis, autosomal dominant leucoencephalopathy syndrome"
+BMGC_DS17545,BMG_DS067183,778062008,Diffuse palmoplantar keratoderma with painful fissures,,,,,,,C4755309,,,MONDO:0018250,diffuse palmoplantar keratoderma with painful fissures,Diffuse palmoplantar keratoderma with painful fissures | Diffuse palmoplantar keratoderma with painful fissures (disorder)
+BMGC_DS17546,BMG_DS067186,778065005,Combined oxidative phosphorylation defect type 14,,,,,,,C4755312,,614946,MONDO:0013986,combined oxidative phosphorylation defect type 14,Combined oxidative phosphorylation defect type 14 | Combined oxidative phosphorylation defect type 14 (disorder) | COXPD14 - combined oxidative phosphorylation defect type 14
+BMGC_DS17547,BMG_DS067189,780817000,Undifferentiated myeloproliferative disease,,,,,,,C4757947,,,,,CMPD-U - chronic myeloproliferative disease unclassifiable | Undifferentiated myeloproliferative disease (disorder) | Undifferentiated myeloproliferative disease
+BMGC_DS17548,BMG_DS067190,780820008,Isolated ATP synthase deficiency,,,,,DOID:0111143,mitochondrial complex V (ATP synthase) deficiency,C4757950,,,MONDO:0014471,mitochondrial proton-transporting ATP synthase complex deficiency,Isolated mitochondrial respiratory chain complex V deficiency | Isolated ATP synthase deficiency | Isolated adenosine triphosphate synthase deficiency (disorder) | Isolated adenosine triphosphate synthase deficiency
+BMGC_DS17549,BMG_DS067364,191020009;238121000,Iodine deficiency,,,,,,,C4759669,,,,,Iodine deficiency | Iodine deficiency (disorder)
+BMGC_DS17550,BMG_DS067365,784339002,Deficiency of interleukin 36 receptor antagonist,,,,,,,C4759670,,,,,DITRA - deficiency of interleukin 36 receptor antagonist | Deficiency of IL-36R antagonist | Deficiency of interleukin 36 receptor antagonist | Deficiency of interleukin 36 receptor antagonist (disorder) | Deficiency of IL-36Ra (interleukin 36 receptor antagonist)
+BMGC_DS17551,BMG_DS067368,,Diabetic Glomerulosclerosis,Diabetic Nephropathies,,,,,,C4759706,D003928,,,,
+BMGC_DS17552,BMG_DS067373,,,,,,,,,C4759728,,612400,MONDO:0012893,osteoarthritis susceptibility 5,
+BMGC_DS17553,BMG_DS067374,111304003;784006008,Spondylometaphyseal dysplasia,,,,,,,C4759767,,MTHU002631,MONDO:0016763,spondylometaphyseal dysplasia,Kozlowski spondylometaphyseal dysplasia | Kozlowski spondylometaphyseal dysplasia (disorder) | Spondylometaphyseal dysplasia Kozlowski type | Spondylometaphyseal dysplasia | Spondylometaphyseal dysplasia (disorder)
+BMGC_DS17554,BMG_DS067375,,"Scapuloperoneal Myopathy, MYH7-Related","Muscular Dystrophy, Emery-Dreifuss",,,,,,C4759774,D020389,,,,
+BMGC_DS17555,BMG_DS067376,,"INTELLECTUAL DISABILITY-HYPOTONIC FACIES SYNDROME, X-LINKED, 1",,,,,,,C4759781,,309580,MONDO:0010663,"intellectual disability-hypotonic facies syndrome, X-linked, 1",
+BMGC_DS17556,BMG_DS067380,,"EPILEPSY, FAMILIAL TEMPORAL LOBE, 2",,,,,DOID:0060755,familial temporal lobe epilepsy 2,C4759869,,608096,MONDO:0011965,familial temporal lobe epilepsy 2,
+BMGC_DS17557,BMG_DS067381,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY 1",,,,,,,C4759870,,607198;607250,MONDO:0011801,"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1",
+BMGC_DS17558,BMG_DS067382,,"DEAFNESS, AUTOSOMAL DOMINANT 37",,,,,DOID:0070601,autosomal dominant nonsyndromic deafness 37,C4760307,,618533;120280,MONDO:0032802,"hearing loss, autosomal dominant 37",
+BMGC_DS17559,BMG_DS067384,,Arthrosis,Osteoarthritis,,,,,,C4760573,D010003,,,,
+BMGC_DS17560,BMG_DS067385,,FETAL AKINESIA DEFORMATION SEQUENCE 2,,,,,DOID:0111378,fetal akinesia deformation sequence syndrome 2,C4760576,,601592;618388,MONDO:0100102,fetal akinesia deformation sequence 2,
+BMGC_DS17561,BMG_DS067386,,FETAL AKINESIA DEFORMATION SEQUENCE 4,,,,,DOID:0111379,fetal akinesia deformation sequence syndrome 4,C4760578,,602552;618393,MONDO:0100104,fetal akinesia deformation sequence 4,
+BMGC_DS17562,BMG_DS067387,,"DEAFNESS, AUTOSOMAL RECESSIVE 99",,,,,DOID:0111634,autosomal recessive nonsyndromic deafness 99,C4760579,,618481;616178,MONDO:0032776,"hearing loss, autosomal recessive 99",
+BMGC_DS17563,BMG_DS067388,,COFFIN-SIRIS SYNDROME 10,,,,,DOID:0112371,Coffin-Siris syndrome 10,C4760583,,618506,MONDO:0032791,Coffin-Siris syndrome 10,
+BMGC_DS17564,BMG_DS067389,,FETAL AKINESIA DEFORMATION SEQUENCE 3,,,,,DOID:0111376,fetal akinesia deformation sequence syndrome 3,C4760599,,618389;610285,MONDO:0100103,fetal akinesia deformation sequence 3,
+BMGC_DS17565,BMG_DS067390,,,,,,,,,C4760647,,618477,MONDO:0032773,uridine-cytidineuria,
+BMGC_DS17566,BMG_DS067391,785808002,Aneurysm osteoarthritis syndrome,,,,,,,C4760764,,,,,Aneurysm osteoarthritis syndrome (disorder) | Aneurysm osteoarthritis syndrome
+BMGC_DS17567,BMG_DS067392,782696001,Recessive mitochondrial ataxia syndrome,,,,,,,C4760799,,,MONDO:0019791,recessive mitochondrial ataxia syndrome,Recessive mitochondrial ataxia syndrome (disorder) | Recessive mitochondrial ataxia syndrome | MIRAS - mitochondrial recessive ataxia syndrome
+BMGC_DS17568,BMG_DS067393,,Familial Horizontal Gaze Palsy with Progressive Scoliosis,,,,,,,C4760875,C564593,,MONDO:0011810,horizontal gaze palsy with progressive scoliosis,
+BMGC_DS17569,BMG_DS067394,783789002,Autosomal recessive brachyolmia,,,,,,,C4760908,,,MONDO:0018662,autosomal recessive brachyolmia,Autosomal recessive brachyolmia (disorder) | Autosomal recessive brachyolmia | Brachyolmia Hobaek/Toledo type
+BMGC_DS17570,BMG_DS067395,,,,,,,,,C4760957,,,MONDO:0016676,recurrent infections-inflammatory syndrome due to zinc metabolism disorder syndrome,
+BMGC_DS17571,BMG_DS067398,,Muscle-Specific Receptor Tyrosine Kinase Myasthenia Gravis,Myasthenia Gravis,,,,,,C4761103,D009157,,,,
+BMGC_DS17572,BMG_DS067406,1228875006,GCGR-related hyperglucagonemia,,,,,,,C4763635,,619290,MONDO:0018582,GCGR-related hyperglucagonemia,Glucagon receptor-related hyperglucagonemia (disorder) | Mahvash disease | Glucagon receptor-related hyperglucagonaemia | GCGR-related hyperglucagonemia | GCGR-related hyperglucagonaemia | Glucagon receptor-related hyperglucagonemia
+BMGC_DS17573,BMG_DS067410,,,,,,,,,C5139324,,,MONDO:0013907,bilateral generalized polymicrogyria,
+BMGC_DS17574,BMG_DS067494,782719004,Autosomal recessive cerebellar ataxia due to STUB1 deficiency,,,,,,,C5190574,,615768,MONDO:0014339,autosomal recessive spinocerebellar ataxia 16,Autosomal recessive cerebellar ataxia due to STUB1 deficiency | Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency (disorder) | Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency | Spinocerebellar ataxia autosomal recessive type 16 | Autosomal recessive cerebellar ataxia due to STUB1 (STIP1 homology and U-box containing protein 1) deficiency | SCAR16 - spinocerebellar ataxia autosomal recessive type 16
+BMGC_DS17575,BMG_DS067495,782720005,Congenital pontocerebellar hypoplasia type 10,,,,,,,C5190575,,615803,MONDO:0014349,pontocerebellar hypoplasia type 10,Congenital pontocerebellar hypoplasia type 10 (disorder) | Congenital pontocerebellar hypoplasia type 10 | CLP1-related pontocerebellar hypoplasia | CLP1 (cleavage and polyadenylation factor I subunit 1) related pontocerebellar hypoplasia
+BMGC_DS17576,BMG_DS067496,782723007,"Severe intellectual disability, progressive spastic diplegia syndrome",,,,,,,C5190576,,,,,"Severe intellectual disability, progressive spastic diplegia syndrome (disorder) | Severe intellectual disability, progressive spastic diplegia syndrome"
+BMGC_DS17577,BMG_DS067497,782725000,Autosomal recessive spastic paraplegia type 69,,,,,,,C5190577,,,MONDO:0018421,autosomal recessive spastic paraplegia type 69,Autosomal recessive spastic paraplegia type 69 | Autosomal recessive spastic paraplegia type 69 (disorder)
+BMGC_DS17578,BMG_DS067498,782726004,Autosomal recessive spastic paraplegia type 71,,,,,,,C5190578,,,MONDO:0018423,autosomal recessive spastic paraplegia type 71,Autosomal recessive spastic paraplegia type 71 | Autosomal recessive spastic paraplegia type 71 (disorder)
+BMGC_DS17579,BMG_DS067500,782736007,"Intellectual disability, facial dysmorphism syndrome due to SETD5 haploinsufficiency",,,,,,,C5190582,,,,,"Intellectual disability, facial dysmorphism syndrome due to SET domain containing 5 haploinsufficiency (disorder) | Intellectual disability, facial dysmorphism syndrome due to SETD5 haploinsufficiency | Intellectual disability, facial dysmorphism syndrome due to SET domain containing 5 haploinsufficiency"
+BMGC_DS17580,BMG_DS067501,782737003,"Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome",,,,,,,C5190583,,,,,"Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome | Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome (disorder)"
+BMGC_DS17581,BMG_DS067503,782742006,Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons,,,,,,,C5190585,,,,,Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons | Autosomal dominant hereditary motor and sensory neuropathy type 2 with giant axons | Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons (disorder)
+BMGC_DS17582,BMG_DS067504,782743001,Huntington disease-like syndrome due to C9ORF72 expansions,,,,,,,C5190586,,,MONDO:0018425,Huntington disease-like syndrome due to C9ORF72 expansions,Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions (disorder) | Huntington disease-like syndrome due to C9ORF72 expansions | Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions | C9ORF72-related Huntington disease phenocopy
+BMGC_DS17583,BMG_DS067505,782744007,Lipoic acid synthetase deficiency,,,,,,,C5190587,,,,,Lipoic acid synthetase deficiency (disorder) | Lipoic acid synthetase deficiency
+BMGC_DS17584,BMG_DS067506,782745008,Lipoyl transferase 1 deficiency,,,,,,,C5190588,,,,,Lipoyl transferase 1 deficiency (disorder) | Lipoyl transferase 1 deficiency
+BMGC_DS17585,BMG_DS067507,782746009,Autosomal recessive spastic paraplegia type 60,,,,,,,C5190589,,,MONDO:0018417,autosomal recessive spastic paraplegia type 60,Autosomal recessive spastic paraplegia type 60 | Autosomal recessive spastic paraplegia type 60 (disorder)
+BMGC_DS17586,BMG_DS067508,782747000,Autosomal recessive spastic paraplegia type 66,,,,,,,C5190590,,,MONDO:0018418,autosomal recessive spastic paraplegia type 66,Autosomal recessive spastic paraplegia type 66 | Autosomal recessive spastic paraplegia type 66 (disorder)
+BMGC_DS17587,BMG_DS067510,782751003,Severe combined immunodeficiency due to IKK2 deficiency,,,,,,,C5190593,,,,,Severe combined immunodeficiency due to inhibitor of nuclear factor kappa B kinase subunit beta deficiency | Severe combined immunodeficiency due to inhibitor of nuclear factor kappa B kinase subunit beta deficiency (disorder) | Severe combined immunodeficiency due to IKK2 deficiency
+BMGC_DS17588,BMG_DS067511,782752005,"Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome",,,,,,,C5190594,,,,,"Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome | Peripheral neuropathy, myopathy, hoarseness, deafness syndrome | Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (disorder)"
+BMGC_DS17589,BMG_DS067512,782753000,"Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome",,,,,,,C5190595,,616354,MONDO:0014601,autosomal recessive spinocerebellar ataxia 20,"Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | SCAR20 - autosomal recessive spinocerebellar ataxia type 20 | Autosomal recessive spinocerebellar ataxia type 20 | Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome (disorder)"
+BMGC_DS17590,BMG_DS067513,782754006,"Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome",,,,,DOID:0070531,foveal hypoplasia 2,C5190596,,,,,"Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome (disorder) | Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome | FHONDA (foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis) syndrome | FHONDA syndrome"
+BMGC_DS17591,BMG_DS067514,782755007,"Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome",,,,,,,C5190597,,,MONDO:0018320,primary microcephaly-mild intellectual disability-young-onset diabetes syndrome,"Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (disorder) | Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome"
+BMGC_DS17592,BMG_DS067517,782759001,X-linked dyserythropoietic anemia with abnormal platelets and neutropenia,,,,,,,C5190600,,,,,X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (disorder) | X-linked dyserythropoietic anemia with abnormal platelets and neutropenia | X-linked dyserythropoietic anaemia with abnormal platelets and neutropenia
+BMGC_DS17593,BMG_DS067518,782771007,Mitochondrial DNA depletion syndrome hepatocerebrorenal form,,,,,,,C5190602,,,MONDO:0018197,"mitochondrial DNA depletion syndrome, hepatocerebrorenal form",Mitochondrial DNA depletion syndrome hepatocerebrorenal form | Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form (disorder) | Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form
+BMGC_DS17594,BMG_DS067519,782772000,Congenital muscular dystrophy with intellectual disability and severe epilepsy,,,,,,,C5190603,,615042,MONDO:0014023,congenital muscular dystrophy with intellectual disability and severe epilepsy,Congenital muscular dystrophy with intellectual disability and severe epilepsy | Congenital muscular dystrophy with intellectual disability and severe epilepsy (disorder) | Congenital disorder of glycosylation type 1u | Carbohydrate deficient glycoprotein syndrome type 1u
+BMGC_DS17595,BMG_DS067520,782773005,Lethal arteriopathy syndrome due to fibulin-4 deficiency,,,,,,,C5190604,,,MONDO:0017818,lethal arteriopathy syndrome due to fibulin-4 deficiency,Lethal arteriopathy syndrome due to fibulin-4 deficiency (disorder) | Lethal arteriopathy syndrome due to fibulin-4 deficiency
+BMGC_DS17596,BMG_DS067523,782781006,High bone mass osteogenesis imperfecta,,,,,,,C5190607,,,MONDO:0017791,high bone mass osteogenesis imperfecta,High bone mass osteogenesis imperfecta | High bone mass osteogenesis imperfecta (disorder)
+BMGC_DS17597,BMG_DS067524,782782004,Autosomal recessive spondylometaphyseal dysplasia Megarbane type,,,,,,,C5190608,,,,,Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Autosomal recessive spondylometaphyseal dysplasia Megarbane type
+BMGC_DS17598,BMG_DS067525,782785002,X-linked osteoporosis with fractures,,,,,,,C5190610,,,MONDO:0018315,X-linked osteoporosis with fractures,X-linked osteoporosis with fractures | X-linked osteoporosis with fractures (disorder)
+BMGC_DS17599,BMG_DS067526,782786001,X-linked calvarial hyperostosis,,,,,,,C5190611,,302030,MONDO:0010541,X-linked calvarial hyperostosis,X-linked calvarial hyperostosis | X-linked calvarial hyperostosis (disorder)
+BMGC_DS17600,BMG_DS067529,782823001,Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome,,,,,,,C5190630,,,,,Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome (disorder) | Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome
+BMGC_DS17601,BMG_DS067530,782824007,Sodium channelopathy-related small fiber neuropathy,,,,,,,C5190631,,,,,Sodium channelopathy-related small fibre neuropathy | Sodium channelopathy-related small fiber neuropathy | Sodium channelopathy-related small fiber neuropathy (disorder)
+BMGC_DS17602,BMG_DS067531,782825008,"Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome",,,,,,,C5190632,,,,,"Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome | Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome (disorder)"
+BMGC_DS17603,BMG_DS067532,782828005,Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency,,,,,,,C5190633,,,,,Developmental delay due to ALDH6A1 (aldehyde dehydrogenase 6 family member A1) deficiency | Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency (disorder) | Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency | Developmental delay due to MMSDH (methylmalonate semialdehyde dehydrogenase) deficiency
+BMGC_DS17604,BMG_DS067535,782878007,Autosomal recessive nail dysplasia,,,,,,,C5190687,,,,,Autosomal recessive nail dysplasia | Autosomal recessive nail dysplasia (disorder)
+BMGC_DS17605,BMG_DS067536,782880001,Hemoglobinopathy Toms River,,,,,,,C5190689,,,MONDO:0017238,hemoglobinopathy Toms River,Haemoglobinopathy Toms River | Hemoglobinopathy Toms River (disorder) | Hemoglobinopathy Toms River | Transient neonatal cyanosis and anemia due to Toms River Hemoglobin | Transient neonatal cyanosis and anaemia due to Toms River Haemoglobin
+BMGC_DS17606,BMG_DS067537,782881002,Hereditary sensorimotor neuropathy with hyperelastic skin,,,,,,,C5190690,,,MONDO:0017237,hereditary sensorimotor neuropathy with hyperelastic skin,Hereditary sensorimotor neuropathy with hyperelastic skin (disorder) | Hereditary sensorimotor neuropathy with hyperelastic skin
+BMGC_DS17607,BMG_DS067538,782883004,Fatal infantile hypertonic myofibrillar myopathy,,,,,,,C5190691,,613869,MONDO:0013472,fatal infantile hypertonic myofibrillar myopathy,Fatal infantile hypertonic myofibrillar myopathy (disorder) | Fatal infantile hypertonic myofibrillar myopathy
+BMGC_DS17608,BMG_DS067539,782886007,"Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome",,,,,,,C5190692,,,MONDO:0016981,infantile spams-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome,"Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome (disorder) | Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome"
+BMGC_DS17609,BMG_DS067540,782887003,Inherited congenital spastic tetraplegia,,,,,,,C5190693,,,,,Inherited congenital spastic tetraplegia | Inherited congenital spastic quadriplegia | Inherited congenital spastic tetraplegia (disorder)
+BMGC_DS17610,BMG_DS067543,782909004,Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation,,,,,,,C5190706,,,MONDO:0015801,hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation,Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation | Haemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation | Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation (disorder)
+BMGC_DS17611,BMG_DS067544,782911008,Hereditary cryohydrocytosis with reduced stomatin,,,,,,,C5190707,,,,,Hereditary cryohydrocytosis with reduced stomatin | Hereditary cryohydrocytosis with reduced stomatin (disorder) | sdCHC - stomatin-deficient cryohydrocytosis | Hereditary cryohydrocytosis type 2 | CHC (hereditary cryohydrocytosis) type 2 | Stomatin-deficient cryohydrocytosis
+BMGC_DS17612,BMG_DS067546,782914000,"Brachydactyly, short stature, retinitis pigmentosa syndrome",,,,,,,C5190709,,,,,"Brachydactyly, short stature, retinitis pigmentosa syndrome (disorder) | Brachydactyly, short stature, retinitis pigmentosa syndrome"
+BMGC_DS17613,BMG_DS067564,783007005,Recurrent Neisseria infection due to factor D deficiency,,,,,,,C5190780,,,,,Recurrent Neisseria infection due to factor D deficiency | Recurrent Neisseria infection due to factor D deficiency (disorder)
+BMGC_DS17614,BMG_DS067571,783055005,Progressive myoclonic epilepsy type 5,,,,,,,C5190799,,,,,Progressive myoclonic epilepsy type 5 (disorder) | Progressive myoclonus epilepsy type 5 | Progressive myoclonic epilepsy type 5 | PME (progressive myoclonic epilepsy) type 5
+BMGC_DS17615,BMG_DS067573,783059004,Atypical dentin dysplasia due to SMOC2 deficiency,,,,,,,C5190802,,,MONDO:0017819,atypical dentin dysplasia due to SMOC2 deficiency,Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency (disorder) | Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency | Atypical dentin dysplasia due to SMOC2 deficiency | Dentin dysplasia type 1 with microdontia and shape anomalies
+BMGC_DS17616,BMG_DS067574,783060009,"Autosomal recessive cerebellar ataxia, psychomotor delay syndrome",,,,,,,C5190803,,614229,MONDO:0013645,autosomal recessive spinocerebellar ataxia 11,"Autosomal recessive cerebellar ataxia, psychomotor delay syndrome (disorder) | Autosomal recessive cerebellar ataxia, psychomotor delay syndrome | Autosomal recessive spinocerebellar ataxia type 11"
+BMGC_DS17617,BMG_DS067575,783061008,"Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion",,,,,,,C5190804,,,MONDO:0017283,DeSanto-Shinawi Syndrome due to 10p11.21p12.31 microdeletion,"Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion (disorder) | Monosomy 10p11.21p12.31 | Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion | 10p12p11 microdeletion syndrome | Deletion 10p11.21p12.31 | Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion"
+BMGC_DS17618,BMG_DS067576,783062001,Progressive myoclonic epilepsy type 6,,,,,,,C5190805,,614018,MONDO:0013526,progressive myoclonic epilepsy type 6,Progressive myoclonic epilepsy type 6 (disorder) | Progressive myoclonic epilepsy type 6 | North Sea progressive myoclonus epilepsy | Progressive myoclonus epilepsy type 6 | GOSR2 (golgi SNAP receptor complex member 2) related progressive myoclonus ataxia | GOSR2-related progressive myoclonus ataxia | PME (progressive myoclonic epilepsy) type 6
+BMGC_DS17619,BMG_DS067577,783065004,Autosomal recessive optic atrophy type 7,,,,,,,C5190807,,,,,Autosomal recessive optic atrophy OPA7 type | Autosomal recessive optic atrophy OPA7 (optic atrophy type 7) | Autosomal recessive optic atrophy type 7 (disorder) | Autosomal recessive optic atrophy type 7
+BMGC_DS17620,BMG_DS067578,783089006,"Macrocephaly, intellectual disability, autism syndrome",,,,,,,C5190809,,,,,"Macrocephaly, intellectual disability, autism syndrome (disorder) | Macrocephaly, intellectual disability, autism syndrome"
+BMGC_DS17621,BMG_DS067579,783091003,"46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome",,,,,,,C5190810,,,,,"46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome | 46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome (disorder)"
+BMGC_DS17622,BMG_DS067580,783092005,"46,XY disorder of sex development, adrenal insufficiency due to CYP11A1 deficiency",,,,,,,C5190811,,,,,"46,XY disorder of sex development, adrenal insufficiency due to cytochrome P450 family 11 subfamily A member 1 deficiency | 46,XY disorder of sex development, adrenal insufficiency due to cytochrome P450 family 11 subfamily A member 1 deficiency (disorder) | XY sex reversal adrenal failure | 46,XY disorder of sex development, adrenal insufficiency due to CYP11A1 deficiency"
+BMGC_DS17623,BMG_DS067582,783098009,Short stature due to partial growth hormone receptor deficiency,,,,,,,C5190814,,,,,Short stature due to partial growth hormone receptor deficiency | Short stature due to partial growth hormone receptor deficiency (disorder) | Short stature due to partial GHR (growth hormone receptor) deficiency
+BMGC_DS17624,BMG_DS067583,783136007,Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering,,,,,,,C5190822,,,,,Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering | Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering (disorder)
+BMGC_DS17625,BMG_DS067586,783139000,Progressive myoclonic epilepsy type 8,,,,,,,C5190825,,616230,MONDO:0014545,progressive myoclonic epilepsy type 8,Progressive myoclonic epilepsy type 8 (disorder) | Progressive myoclonic epilepsy type 8 | Progressive myoclonus epilepsy type 8 | Progressive myoclonic epilepsy due to CERS1 (ceramide synthase 1) deficiency | Progressive myoclonic epilepsy due to ceramide synthase 1 deficiency | PME (progressive myoclonic epilepsy) type 8
+BMGC_DS17626,BMG_DS067587,783142006,Pancytopenia due to IKZF1 mutations,,,,,,,C5190826,,,,,Pancytopenia due to IKZF1 mutations | Pancytopenia due to IKAROS family zinc finger 1 mutations (disorder) | Combined immunodeficiency due to IKAROS deficiency | Pancytopenia due to IKAROS family zinc finger 1 mutations
+BMGC_DS17627,BMG_DS067588,783148005,Distal nebulin myopathy,,,,,,,C5190827,,,MONDO:0018371,nebulin-related early-onset distal myopathy,Distal nebulin myopathy | Nebulin-related early-onset distal myopathy | Distal nebulin myopathy (disorder)
+BMGC_DS17628,BMG_DS067594,783161005,Familial dementia British type,,,,,,,C5190835,,176500,MONDO:0008306,ABri amyloidosis,Familial dementia British type (disorder) | Familial dementia British type | ABri amyloidosis | Familial British dementia with amyloid angiopathy
+BMGC_DS17629,BMG_DS067597,783174004,Congenital muscular dystrophy with intellectual disability,,,,,,,C5190846,,,MONDO:0018278,congenital muscular dystrophy with intellectual disability,Congenital muscular dystrophy with intellectual disability | Congenital muscular dystrophy with intellectual disability (disorder)
+BMGC_DS17630,BMG_DS067598,783175003,Congenital muscular dystrophy without intellectual disability,,,,,,,C5190847,,,MONDO:1040033,congenital muscular dystrophy without intellectual disability,Congenital muscular dystrophy without intellectual disability (disorder) | Congenital muscular dystrophy without intellectual disability
+BMGC_DS17631,BMG_DS067599,783176002,Congenital muscular dystrophy with cerebellar involvement,,,,,,,C5190848,,,,,Congenital muscular dystrophy with cerebellar involvement | Congenital muscular dystrophy with cerebellar involvement (disorder)
+BMGC_DS17632,BMG_DS067604,783182004,Chronic respiratory distress with surfactant metabolism deficiency,,,,,,,C5190853,,,MONDO:0016323,chronic respiratory distress with surfactant metabolism deficiency,Chronic respiratory distress with surfactant metabolism deficiency (disorder) | Chronic respiratory distress with surfactant metabolism deficiency
+BMGC_DS17633,BMG_DS067609,783198006,Hereditary sensory and autonomic neuropathy due to tectonin beta-propeller repeat containing 2 mutation,,,,,,,C5190860,,,,,Hereditary sensory and autonomic neuropathy due to TECPR2 mutation | Hereditary sensory and autonomic neuropathy due to tectonin beta-propeller repeat containing 2 mutation (disorder) | Hereditary sensory and autonomic neuropathy due to tectonin beta-propeller repeat containing 2 mutation | Autosomal recessive spastic paraplegia type 49 | Hereditary sensory and autonomic neuropathy due to TECPR2 (tectonin beta-propeller repeat containing 2) mutation
+BMGC_DS17634,BMG_DS067610,783199003,Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency,,,,,,,C5190861,,,,,Autosomal recessive severe congenital neutropenia due to JAGN1 (jagunal homolog 1) deficiency | Autosomal recessive severe congenital neutropenia due to jagunal homolog 1 deficiency | Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency | Autosomal recessive severe congenital neutropenia due to jagunal homolog 1 deficiency (disorder)
+BMGC_DS17635,BMG_DS067611,783200000,Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency,,,,,,,C5190862,,,MONDO:0018487,autosomal recessive severe congenital neutropenia due to CXCR2 deficiency,Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 deficiency | Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency | Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 deficiency (disorder) | Autosomal recessive severe congenital neutropenia due to CXCR2 (C-X-C motif chemokine receptor 2) deficiency
+BMGC_DS17636,BMG_DS067612,783201001,Autosomal recessive severe congenital neutropenia due to CSF3R deficiency,,,,,,,C5190863,,,,,Autosomal recessive severe congenital neutropenia due to CSF3R (colony stimulating factor 3 receptor) deficiency | Autosomal recessive severe congenital neutropenia due to CSF3R deficiency | Autosomal recessive severe congenital neutropenia due to colony stimulating factor 3 receptor deficiency | Autosomal recessive severe congenital neutropenia due to colony stimulating factor 3 receptor deficiency (disorder)
+BMGC_DS17637,BMG_DS067613,783202008,Autosomal dominant secondary polycythemia,,,,,,,C5190864,,,,,Autosomal dominant secondary polycythemia (disorder) | Autosomal dominant secondary polycythemia | Autosomal dominant secondary polycythaemia | Autosomal dominant secondary erythrocytosis
+BMGC_DS17638,BMG_DS067619,783245001,Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection,,,,,,,C5190882,,,,,Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection (disorder) | Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection | Primary immunodeficiency with post-MMR (measles-mumps-rubella) vaccine viral infection
+BMGC_DS17639,BMG_DS067620,783246000,"Megalocornea, spherophakia, secondary glaucoma syndrome",,,,,,,C5190883,,,MONDO:0016559,glaucoma secondary to spherophakia/ectopia lentis and megalocornea,"Megalocornea, spherophakia, secondary glaucoma syndrome (disorder) | Megalocornea, spherophakia, secondary glaucoma syndrome"
+BMGC_DS17640,BMG_DS067623,783250007,Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency,,,,,,,C5190887,,,,,Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency | Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency (disorder)
+BMGC_DS17641,BMG_DS067625,783254003,Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome,,,,,,,C5190890,,,MONDO:0016672,hereditary persistence of fetal hemoglobin-sickle cell disease syndrome,Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome | Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome | Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome (disorder)
+BMGC_DS17642,BMG_DS067626,783255002,Hereditary isolated aplastic anemia,,,,,,,C5190891,,,,,Hereditary isolated aplastic anemia | Hereditary isolated aplastic anemia (disorder) | Hereditary isolated aplastic anaemia
+BMGC_DS17643,BMG_DS067628,783549006,Obesity due to CEP19 deficiency,,,,,,,C5190985,,,,,Obesity due to centrosomal protein 19 deficiency | Obesity due to CEP19 deficiency | Obesity due to centrosomal protein 19 deficiency (disorder)
+BMGC_DS17644,BMG_DS067629,783551005,"Ichthyosis, short stature, brachydactyly, microspherophakia syndrome",,,,,,,C5190986,,,,,"Ichthyosis, short stature, brachydactyly, microspherophakia syndrome | Ichthyosis, short stature, brachydactyly, microspherophakia syndrome (disorder) | 15q26.3 microdeletion syndrome"
+BMGC_DS17645,BMG_DS067630,783554002,Autosomal recessive limb girdle muscular dystrophy type 2U,,,,,,,C5190987,,616052,MONDO:0014474,autosomal recessive limb-girdle muscular dystrophy type 2U,Autosomal recessive limb girdle muscular dystrophy type 2U | Autosomal recessive limb girdle muscular dystrophy type 2U (disorder) | Autosomal recessive limb girdle muscular dystrophy due to ISPD deficiency | LGMD2U - autosomal recessive limb girdle muscular dystrophy type 2U
+BMGC_DS17646,BMG_DS067632,783556000,Severe early-onset obesity insulin resistance syndrome due to SH2B1 deficiency,,,,,,,C5190989,,,MONDO:0017994,severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency,Severe early-onset obesity insulin resistance syndrome due to SH2B adaptor protein 1 deficiency (disorder) | Severe early-onset obesity insulin resistance syndrome due to SH2B1 deficiency | Severe early-onset obesity insulin resistance syndrome due to SH2B adaptor protein 1 deficiency
+BMGC_DS17647,BMG_DS067633,783558004,Combined oxidative phosphorylation defect type 11,,,,,,,C5190991,,614922,MONDO:0013969,combined oxidative phosphorylation defect type 11,Combined oxidative phosphorylation defect type 11 | COXPD11 - combined oxidative phosphorylation defect type 11 | Combined oxidative phosphorylation defect type 11 (disorder)
+BMGC_DS17648,BMG_DS067638,783614008,Familial steroid-resistant nephrotic syndrome with sensorineural deafness,,,,,,,C5191003,,,,,Familial steroid-resistant nephrotic syndrome with sensorineural deafness (disorder) | Familial steroid-resistant nephrotic syndrome with sensorineural deafness
+BMGC_DS17649,BMG_DS067640,783616005,Perilipin 1 related familial partial lipodystrophy,,,,,,,C5191005,,613877,MONDO:0013478,PLIN1-related familial partial lipodystrophy,PLIN1-related familial partial lipodystrophy | Perilipin 1 related familial partial lipodystrophy (disorder) | FPLD4 - familial partial lipodystrophy type 4 | Perilipin 1 related familial partial lipodystrophy
+BMGC_DS17650,BMG_DS067641,783617001,Severe combined immunodeficiency due to LCK deficiency,,,,,,,C5191006,,,,,Severe combined immunodeficiency due to lymphocyte-specific protein-tyrosine kinase deficiency (disorder) | Severe combined immunodeficiency due to LCK (lymphocyte-specific protein-tyrosine kinase) deficiency | Severe combined immunodeficiency due to lymphocyte-specific protein-tyrosine kinase deficiency | Severe combined immunodeficiency due to LCK deficiency
+BMGC_DS17651,BMG_DS067642,783618006,Lower motor neuron syndrome with late-adult onset,,,,,,,C5191007,,,,,Lower motor neuron syndrome with late-adult onset (disorder) | Lower motor neuron syndrome with late-adult onset
+BMGC_DS17652,BMG_DS067643,783619003,DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion,,,,,,,C5191008,,,MONDO:0017056,DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion,Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion (disorder) | DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion | Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion | 21q22.13q22.2 microdeletion syndrome | Monosomy 21q22.13q22.2
+BMGC_DS17653,BMG_DS067644,783620009,Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis,,,,,,,C5191009,,,,,Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis | Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis (disorder) | Dominant hypophosphataemia with nephrolithiasis and/or osteoporosis
+BMGC_DS17654,BMG_DS067645,783621008,Immunodeficiency with factor I anomaly,,,,,,,C5191010,,,,,Complete factor I deficiency | Immunodeficiency with factor I anomaly (disorder) | Immunodeficiency with factor I anomaly
+BMGC_DS17655,BMG_DS067648,783702009,X-linked intellectual disability due to GRIA3 mutations,,,,,,,C5191041,,,,,X-linked intellectual disability due to GRIA3 mutations | X-linked intellectual disability due to glutamate ionotropic receptor AMPA type subunit 3 mutations | X-linked intellectual disability due to glutamate ionotropic receptor AMPA type subunit 3 mutations (disorder)
+BMGC_DS17656,BMG_DS067651,783719006,Obesity due to SIM1 deficiency,,,,,,,C5191050,,,MONDO:0018244,obesity due to SIM1 deficiency,Obesity due to SIM bHLH transcription factor 1 deficiency | Obesity due to SIM1 deficiency | Obesity due to SIM bHLH transcription factor 1 deficiency (disorder)
+BMGC_DS17657,BMG_DS067655,783734000,"Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency",,,,,,,C5191055,,251880,MONDO:0009636,mitochondrial DNA depletion syndrome 3 (hepatocerebral type),"Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency (disorder) | Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency"
+BMGC_DS17658,BMG_DS067658,783737007,"Hirschsprung disease, ganglioneuroblastoma syndrome",,,,,,,C5191058,,,MONDO:0013082,Hirschsprung disease-ganglioneuroblastoma syndrome,"Hirschsprung disease, ganglioneuroblastoma syndrome (disorder) | Hirschsprung disease, ganglioneuroblastoma syndrome"
+BMGC_DS17659,BMG_DS067659,783740007,Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency,,,,,,,C5191059,,,MONDO:0017187,diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency,"Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency | Diazoxide-resistant focal hyperinsulinism due to sulfonylurea receptor 1 deficiency (disorder) | Diazoxide-resistant focal hyperinsulinism due to sulfonylurea receptor 1 deficiency | Hyperinsulinemic hypoglycaemia due to SUR1 deficiency, diazoxide-resistant focal form | Hyperinsulinemic hypoglycemia due to SUR1 deficiency, diazoxide-resistant focal form"
+BMGC_DS17660,BMG_DS067660,783741006,Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency,,,,,,,C5191060,,,MONDO:0017188,diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency,"Hyperinsulinemic hypoglycaemia due to Kir6.2 deficiency, diazoxide-resistant focal form | Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency | Hyperinsulinemic hypoglycemia due to Kir6.2 deficiency, diazoxide-resistant focal form | Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency (disorder)"
+BMGC_DS17661,BMG_DS067661,783743009,Combined immunodeficiency with granulomatosis,,,,,,,C5191061,,,,,Combined immunodeficiency with granulomatosis | Combined immunodeficiency due to RAG 1/2 deficiency | Combined immunodeficiency with granulomatosis (disorder) | Combined immunodeficiency due to RAG 1/2 (recombination activating gene 1/2) deficiency
+BMGC_DS17662,BMG_DS067662,783766005,Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene,,,,,,,C5191076,,,,,Autosomal recessive secondary polycythaemia not associated with Von Hippel Lindau gene | Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder) | Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene | Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene | Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene | Autosomal recessive secondary polycythemia non-Chuvash type | Autosomal recessive secondary erythrocytosis non-Chuvash type | Autosomal recessive secondary polycythaemia non-Chuvash type
+BMGC_DS17663,BMG_DS067663,783767001,Autosomal recessive hyperinsulinism due to SUR1 deficiency,,,,,,,C5191077,,,MONDO:0019333,autosomal recessive hyperinsulinism due to SUR1 deficiency,Autosomal recessive hyperinsulinism due to sulfonylurea receptor 1 deficiency (disorder) | Autosomal recessive hyperinsulinism due to SUR1 deficiency | Autosomal recessive hyperinsulinism due to sulfonylurea receptor 1 deficiency | Autosomal recessive hyperinsulinemic hypoglycemia due to SUR1 deficiency | Autosomal recessive hyperinsulinemic hypoglycaemia due to SUR1 deficiency
+BMGC_DS17664,BMG_DS067664,783768006,Autosomal recessive hyperinsulinism due to Kir6.2 deficiency,,,,,,,C5191078,,,MONDO:0019334,autosomal recessive hyperinsulinism due to Kir6.2 deficiency,Autosomal recessive hyperinsulinism due to Kir6.2 deficiency | Autosomal recessive hyperinsulinism due to Kir6.2 deficiency (disorder) | Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency | Autosomal recessive hyperinsulinemic hypoglycaemia due to Kir6.2 deficiency
+BMGC_DS17665,BMG_DS067665,783770002,Alpha-B crystallin-related late-onset myopathy,,,,,,,C5191079,,,,,Alpha-B crystallin-related late-onset myopathy | Alpha-B crystallin-related late-onset distal myopathy | Alpha-B crystallin-related late-onset myopathy (disorder) | Late-onset distal crystallinopathy
+BMGC_DS17666,BMG_DS067670,784340000,Combined immunodeficiency due to interleukin 21 receptor deficiency,,,,,,,C5191307,,,,,Combined immunodeficiency due to interleukin 21 receptor deficiency (disorder) | Combined immunodeficiency due to IL21R deficiency | Combined immunodeficiency due to interleukin 21 receptor deficiency
+BMGC_DS17667,BMG_DS067671,784344009,Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation,,,,,,,C5191309,,,,,Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation (disorder) | Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation
+BMGC_DS17668,BMG_DS067672,784348007,Familial congenital mirror movements,,,,,,,C5191311,,,,,Familial congenital controlateral synkinesia | Hereditary congenital mirror movements | Isolated congenital mirror movements | Familial congenital mirror movements | Hereditary congenital controlateral synkinesia | Isolated congenital controlateral synkinesia | Familial congenital mirror movements (disorder)
+BMGC_DS17669,BMG_DS067674,784370005,Mitochondrial myopathy with reversible cytochrome C oxidase deficiency,,,,,,,C5191317,,,,,Mitochondrial myopathy with reversible cytochrome C oxidase deficiency (disorder) | Mitochondrial myopathy with reversible cytochrome C oxidase deficiency | Benign COX (cytochrome C oxidase) deficiency | Mitochondrial myopathy with reversible complex IV deficiency | Reversible infantile cytochrome C oxidase deficiency | Infantile reversible cytochrome C oxidase deficiency myopathy | Reversible infantile respiratory chain deficiency | Mitochondrial myopathy with reversible COX (cytochrome C oxidase) deficiency
+BMGC_DS17670,BMG_DS067675,784372002,Familial mesial temporal lobe epilepsy with febrile seizures,,,,,,,C5191318,,,,,Familial mesial temporal lobe epilepsy with febrile seizures (disorder) | Familial mesial temporal lobe epilepsy with febrile seizures
+BMGC_DS17671,BMG_DS067683,785298001,Muscle eye brain disease with bilateral multicystic leukodystrophy,,,,,,,C5191414,,,MONDO:0018280,muscle-eye-brain disease with bilateral multicystic leucodystrophy,Muscle eye brain disease with bilateral multicystic leucodystrophy | Muscle eye brain disease with bilateral multicystic leukodystrophy | Muscle eye brain disease with bilateral multicystic leukodystrophy (disorder)
+BMGC_DS17672,BMG_DS067684,785303004,"Multiple congenital anomalies, hypotonia, seizures syndrome",,,,,,,C5191419,,,MONDO:0100247,multiple congenital anomalies-hypotonia-seizures syndrome,"Multiple congenital anomalies, hypotonia, seizures syndrome (disorder) | Congenital disorder of glycosylation due to PIGN (phosphatidylinositol glycan anchor biosynthesis class N) deficiency | PIGN-CDG - phosphatidylinositol glycan anchor biosynthesis class N congenital disorder of glycosylation | Multiple congenital anomalies, hypotonia, seizures syndrome"
+BMGC_DS17673,BMG_DS067690,785722006,Obesity due to leptin receptor gene deficiency,,,,,,,C5191640,,,,,Obesity due to leptin receptor gene deficiency | Obesity due to leptin receptor gene deficiency (disorder)
+BMGC_DS17674,BMG_DS067692,785724007,"Pyoderma gangrenosum, acne, suppurative hidradenitis syndrome",,,,,,,C5191642,,,MONDO:0017332,pyoderma gangrenosum-acne-suppurative hidradenitis syndrome,"PASH syndrome | Pyoderma gangrenosum, acne, suppurative hidradenitis syndrome (disorder) | Pyoderma gangrenosum, acne, suppurative hidradenitis syndrome | PASH (pyoderma gangrenosum, acne, suppurative hidradenitis) syndrome"
+BMGC_DS17675,BMG_DS067693,785726009,Hyperekplexia epilepsy syndrome,,,,,,,C5191643,,,,,Hyperekplexia epilepsy syndrome (disorder) | Hyperekplexia epilepsy syndrome
+BMGC_DS17676,BMG_DS067694,785727000,Chronic infantile diarrhea due to guanylate cyclase 2C overactivity,,,,,,,C5191644,,,,,Chronic infantile diarrhea due to guanylate cyclase 2C overactivity (disorder) | Chronic infantile diarrhea due to guanylate cyclase 2C overactivity | Chronic infantile diarrhoea due to guanylate cyclase 2C overactivity
+BMGC_DS17677,BMG_DS067703,,Synucleinopathies,Synucleinopathies,,,,,,C5191670,D000080874,,MONDO:0000510,synucleinopathy,
+BMGC_DS17678,BMG_DS067762,,,,,,,,,C5191836,,,MONDO:0017895,familial papillary or follicular thyroid carcinoma,
+BMGC_DS17679,BMG_DS067813,787093004,"Developmental delay, facial dysmorphism syndrome due to MED13L deficiency",,,,,,,C5192431,,,,,"Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency (disorder) | Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency | Developmental delay, facial dysmorphism syndrome due to MED13L deficiency"
+BMGC_DS17680,BMG_DS067834,787171006,21q22.11q22.12 microdeletion syndrome,,,,,,,C5192593,,,MONDO:0016845,21q22.11q22.12 microdeletion syndrome,21q22.11q22.12 microdeletion syndrome | Monosomy 21q22.11q22.12 | 21q22.11q22.12 microdeletion syndrome (disorder)
+BMGC_DS17681,BMG_DS067835,787172004,Childhood-onset autosomal recessive myopathy with external ophthalmoplegia,,,,,,,C5192594,,,MONDO:0018206,childhood-onset autosomal recessive myopathy with external ophthalmoplegia,Childhood-onset autosomal recessive myopathy with external ophthalmoplegia (disorder) | Childhood-onset autosomal recessive myopathy with external ophthalmoplegia
+BMGC_DS17682,BMG_DS067836,787174003,"Intellectual disability, hyperkinetic movement, truncal ataxia syndrome",,,,,,,C5192595,,,MONDO:0018243,intellectual disability-hyperkinetic movement-truncal ataxia syndrome,"Intellectual disability, hyperkinetic movement, truncal ataxia syndrome (disorder) | Intellectual disability, hyperkinetic movement, truncal ataxia syndrome"
+BMGC_DS17683,BMG_DS067837,787175002,"ANK3-related intellectual disability, sleep disturbance syndrome",,,,,,,C5192596,,,,,"Ankyrin 3 related intellectual disability, sleep disturbance syndrome (disorder) | ANK3-related intellectual disability, sleep disturbance syndrome | Ankyrin 3 related intellectual disability, sleep disturbance syndrome"
+BMGC_DS17684,BMG_DS067843,787410005,Hereditary mixed polyposis syndrome,,,,,,,C5192681,,,MONDO:0011023,hereditary mixed polyposis syndrome,Hereditary mixed polyposis syndrome | Hereditary mixed polyposis syndrome (disorder) | HMPS - hereditary mixed polyposis syndrome
+BMGC_DS17685,BMG_DS067857,783057002,DNA2-related mitochondrial DNA deletion syndrome,,,,,,,C5192959,,,,,Mitochondrial DNA deletion syndrome with limb-girdle weakness | Mitochondrial DNA deletion syndrome with progressive myopathy | DNA2-related mitochondrial DNA deletion syndrome | DNA replication helicase/nuclease 2-related mitochondrial deoxyribonucleic acid deletion syndrome | DNA replication helicase/nuclease 2-related mitochondrial deoxyribonucleic acid deletion syndrome (disorder)
+BMGC_DS17686,BMG_DS067858,,"ARTHROGRYPOSIS, DISTAL, TYPE 2B4",,,,,,,C5193002,,108120;190990,MONDO:0800200,"arthrogryposis, distal, type 2B4",
+BMGC_DS17687,BMG_DS067859,,CALVARIAL DOUGHNUT LESIONS WITH BONE FRAGILITY AND SPONDYLOMETAPHYSEAL DYSPLASIA,,,,,DOID:0080721,calvarial doughnut lesions with bone fragility,C5193004,,126550;611574,MONDO:0800204,calvarial doughnut lesions with bone fragility and spondylometaphyseal dysplasia,
+BMGC_DS17688,BMG_DS067860,,GIST-PLUS SYNDROME,,,,,,,C5193005,,173490;175510,MONDO:0008285,"polyps, multiple and recurrent inflammatory fibroid, gastrointestinal",
+BMGC_DS17689,BMG_DS067861,,D-LACTIC ACIDURIA WITH GOUT,,,,,,,C5193006,,245450,MONDO:0009505,lactic aciduria due to D-lactic acid,
+BMGC_DS17690,BMG_DS067862,,"MITOCHONDRIAL MYOPATHY, EPISODIC, WITH OR WITHOUT OPTIC ATROPHY AND REVERSIBLE LEUKOENCEPHALOPATHY",,,,,,,C5193007,,251900,,,
+BMGC_DS17691,BMG_DS067863,,MULLEGAMA-KLEIN-MARTINEZ SYNDROME,,,,,DOID:0111845,Mullegama-Klein-Martinez syndrome,C5193008,,301022;300826,MONDO:0026722,Mullegama-Klein-Martinez syndrome,
+BMGC_DS17692,BMG_DS067864,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 108",,,,,DOID:0111844,X-linked intellectual developmental disorder 108,C5193009,,300368;301024,MONDO:0026723,"intellectual developmental disorder, X-linked 108",
+BMGC_DS17693,BMG_DS067865,,PAGANINI-MIOZZO SYNDROME,,,,,DOID:0111843,Paganini-Miozzo syndrome,C5193010,,301025;300545,MONDO:0026724,Paganini-Miozzo syndrome,
+BMGC_DS17694,BMG_DS067866,,"NEPHROTIC SYNDROME, TYPE 20",,,,,DOID:0070357,nephrotic syndrome type 20,C5193011,,301028;301027,MONDO:0026726,"nephrotic syndrome, type 20",
+BMGC_DS17695,BMG_DS067867,,"DEAFNESS, Y-LINKED 2",,,,,DOID:0111758,Y-linked deafness 2,C5193013,,400033;400047,MONDO:0027048,"deafness, Y-linked 2",
+BMGC_DS17696,BMG_DS067868,,"ARTHROGRYPOSIS, DISTAL, TYPE 2B1",,,,,DOID:0111600,distal arthrogryposis type 2B1,C5193014,,601680;191043,MONDO:0020820,distal arthrogryposis type 2B1,
+BMGC_DS17697,BMG_DS067869,,CONGENITAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE,,,,,,,C5193016,,611890;603371,MONDO:0012750,lethal arthrogryposis-anterior horn cell disease syndrome,
+BMGC_DS17698,BMG_DS067870,,"MICROPHTHALMIA, SYNDROMIC 15",,,,,,,C5193017,,615145;610083,,,
+BMGC_DS17699,BMG_DS067871,,CONE-ROD DYSTROPHY AND HEARING LOSS 1,,,,,,,C5193018,,617110;617236,MONDO:0020778,cone-rod dystrophy and hearing loss 1,
+BMGC_DS17700,BMG_DS067872,,WARBURG-CINOTTI SYNDROME,,,,,,,C5193019,,191311;618175,MONDO:0032579,warburg-cinotti syndrome,
+BMGC_DS17701,BMG_DS067873,,DIAMOND-BLACKFAN ANEMIA 18,,,,,DOID:0111896,Diamond-Blackfan anemia 18,C5193020,,604179;618310,MONDO:0032668,Diamond-Blackfan anemia 18,
+BMGC_DS17702,BMG_DS067874,,DIAMOND-BLACKFAN ANEMIA 19,,,,,DOID:0111886,Diamond-Blackfan anemia 19,C5193021,,618315;618312,MONDO:0032669,Diamond-Blackfan anemia 19,
+BMGC_DS17703,BMG_DS067875,,DIAMOND-BLACKFAN ANEMIA 20,,,,,DOID:0111891,Diamond-Blackfan anemia 20,C5193022,,618313;603674,MONDO:0032670,Diamond-Blackfan anemia 20,
+BMGC_DS17704,BMG_DS067876,,"HYPOMAGNESEMIA, SEIZURES, AND IMPAIRED INTELLECTUAL DEVELOPMENT 2",,,,,,,C5193023,,182310;618314,MONDO:0020788,"hypomagnesemia, seizures, and intellectual disability 2",
+BMGC_DS17705,BMG_DS067877,1222708006,"TMEM94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome",,,,,,,C5193024,,618316,MONDO:0032672,intellectual developmental disorder with cardiac defects and dysmorphic facies,"Transmembrane protein 94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome | Transmembrane protein 94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome (disorder) | TMEM94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome"
+BMGC_DS17706,BMG_DS067878,,"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 7, AUTOSOMAL RECESSIVE",,,,,,,C5193025,,618255;618317,MONDO:0032673,"basal ganglia calcification, idiopathic, 7, autosomal recessive",
+BMGC_DS17707,BMG_DS067879,1251446004,NAD(P)HX dehydratase deficiency,,,,,,,C5193026,,618321,MONDO:0034121,NAD(P)HX dehydratase deficiency,NAD(P)HX dehydratase deficiency (disorder) | NAD(P)HX dehydratase deficiency | CARKD deficiency
+BMGC_DS17708,BMG_DS067880,,"MYASTHENIC SYNDROME, CONGENITAL, 25, PRESYNAPTIC",,,,,,,C5193027,,618323;185880,MONDO:0032675,"myasthenic syndrome, congenital, 25, presynaptic",
+BMGC_DS17709,BMG_DS067881,,CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION 2,,,,,,,C5193028,,608675;618324,MONDO:0020777,congenital disorder of glycosylation with defective fucosylation 2,
+BMGC_DS17710,BMG_DS067882,,LISSENCEPHALY 9 WITH COMPLEX BRAINSTEM MALFORMATION,,,,,DOID:0112228,lissencephaly 9 with complex brainstem malformation,C5193029,,618325;608271,MONDO:0032677,lissencephaly 9 with complex brainstem malformation,
+BMGC_DS17711,BMG_DS067883,1222662000,Neonatal epileptic encephalopathy due to glutaminase deficiency,,,,,,,C5193030,,618328,MONDO:0032678,"developmental and epileptic encephalopathy, 71",Neonatal epileptic encephalopathy due to glutaminase deficiency | Neonatal epileptic encephalopathy due to deficiency of glutaminase | Neonatal epileptic encephalopathy due to deficiency of glutaminase (disorder)
+BMGC_DS17712,BMG_DS067884,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 37,,,,,DOID:0111499,combined oxidative phosphorylation deficiency 37,C5193031,,618329;616658,MONDO:0032679,combined oxidative phosphorylation deficiency 37,
+BMGC_DS17713,BMG_DS067885,,GLOBAL DEVELOPMENTAL DELAY WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT,,,,,,,C5193032,,618330,MONDO:0032680,global developmental delay with or without impaired intellectual development,
+BMGC_DS17714,BMG_DS067886,,"ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH EPISODIC RHABDOMYOLYSIS",,,,,,,C5193033,,610970;618331,MONDO:0032681,"encephalopathy, progressive, early-onset, with episodic rhabdomyolysis",
+BMGC_DS17715,BMG_DS067887,,MENKE-HENNEKAM SYNDROME 1,,,,,,,C5193034,,600140;618332,MONDO:0020763,Menke-Hennekam syndrome 1,
+BMGC_DS17716,BMG_DS067888,,MENKE-HENNEKAM SYNDROME 2,,,,,,,C5193035,,602700;618333,MONDO:0020769,Menke-Hennekam syndrome 2,
+BMGC_DS17717,BMG_DS067889,,"INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, GENITAL ANOMALIES, AND IMMUNODEFICIENCY",,,,,,,C5193036,,618336;174762,MONDO:0032684,"intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency",
+BMGC_DS17718,BMG_DS067890,,"INFANTILE CATARACT, SKIN ABNORMALITIES, GLUTAMATE EXCESS, AND IMPAIRED INTELLECTUAL DEVELOPMENT",,,,,,,C5193037,,138280;618339,MONDO:0032685,"infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development",
+BMGC_DS17719,BMG_DS067891,,SPERMATOGENIC FAILURE 35,,,,,DOID:0111914,spermatogenic failure 35,C5193038,,618304;618341,MONDO:0032686,spermatogenic failure 35,
+BMGC_DS17720,BMG_DS067892,,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH ABNORMAL BEHAVIOR, MICROCEPHALY, AND SHORT STATURE",,,,,DOID:0081265,"intellectual developmental disorder with abnormal behavior, microcephaly, and short stature",C5193039,,616261;618342,MONDO:0032687,"intellectual developmental disorder with abnormal behavior, microcephaly, and short stature",
+BMGC_DS17721,BMG_DS067893,,POLYMICROGYRIA WITH OR WITHOUT VASCULAR-TYPE EHLERS-DANLOS SYNDROME,,,,,,,C5193040,,618343,MONDO:0032688,polymicrogyria with or without vascular-type Ehlers-Danlos syndrome,
+BMGC_DS17722,BMG_DS067894,,RETINITIS PIGMENTOSA 85,,,,,DOID:0112142,retinitis pigmentosa 85,C5193041,,600253;618345,MONDO:0032689,retinitis pigmentosa 85,
+BMGC_DS17723,BMG_DS067895,,"MICROCEPHALY, GROWTH DEFICIENCY, SEIZURES, AND BRAIN MALFORMATIONS",,,,,DOID:0081051,"microcephaly, growth deficiency, seizures, and brain malformations",C5193042,,618346;605924,MONDO:0032690,"microcephaly, growth deficiency, seizures, and brain malformations",
+BMGC_DS17724,BMG_DS067896,,GALLOWAY-MOWAT SYNDROME 6,,,,,,,C5193043,,618347;605924,MONDO:0032691,Galloway-Mowat syndrome 6,
+BMGC_DS17725,BMG_DS067897,,GALLOWAY-MOWAT SYNDROME 7,,,,,,,C5193044,,618348;607617,MONDO:0032692,Galloway-Mowat syndrome 7,
+BMGC_DS17726,BMG_DS067898,,GALLOWAY-MOWAT SYNDROME 8,,,,,,,C5193045,,618349;607613,MONDO:0032693,Galloway-Mowat syndrome 8,
+BMGC_DS17727,BMG_DS067899,,"MICROCEPHALY 25, PRIMARY, AUTOSOMAL RECESSIVE",,,,,,,C5193046,,618350;618351,MONDO:0032694,"microcephaly 25, primary, autosomal recessive",
+BMGC_DS17728,BMG_DS067900,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 6,,,,,,,C5193047,,182888;618353,MONDO:0032696,oocyte maturation defect 6,
+BMGC_DS17729,BMG_DS067901,,HOUGE-JANSSENS SYNDROME 3,,,,,,,C5193048,,176915;618354,MONDO:0032697,Houge-Janssens syndrome 3,
+BMGC_DS17730,BMG_DS067902,,NEURODEVELOPMENTAL DISORDER WITH CENTRAL AND PERIPHERAL MOTOR DYSFUNCTION,,,,,,,C5193049,,609145;618356,MONDO:0032698,neurodevelopmental disorder with central and peripheral motor dysfunction,
+BMGC_DS17731,BMG_DS067903,,,,,,,,,C5193050,,618357,MONDO:0032699,"epilepsy, idiopathic generalized, susceptibility to, 15",
+BMGC_DS17732,BMG_DS067904,,CONE-ROD DYSTROPHY AND HEARING LOSS 2,,,,,,,C5193051,,609689;618358,MONDO:0020780,cone-rod dystrophy and hearing loss 2,
+BMGC_DS17733,BMG_DS067905,,BRAIN SMALL VESSEL DISEASE 3,,,,,DOID:0112315,brain small vessel disease 3,C5193053,,618360;617531,MONDO:0100105,brain small vessel disease 3,
+BMGC_DS17734,BMG_DS067906,,COFFIN-SIRIS SYNDROME 8,,,,,DOID:0112367,Coffin-Siris syndrome 8,C5193054,,618362;601734,MONDO:0032702,Coffin-Siris syndrome 8,
+BMGC_DS17735,BMG_DS067907,,"SHORT STATURE, AMELOGENESIS IMPERFECTA, AND SKELETAL DYSPLASIA WITH SCOLIOSIS",,,,,,,C5193055,,611459;618363,MONDO:0032703,"short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis",
+BMGC_DS17736,BMG_DS067908,,"MYOCLONUS, FAMILIAL, 2",,,,,,,C5193056,,600702;618364,MONDO:0100092,"myoclonus, familial, 2",
+BMGC_DS17737,BMG_DS067909,1300128003,"MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome",,,,,,,C5193057,,618367,MONDO:0032705,"neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination","MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome | MTHFS (methenyltetrahydrofolate synthetase) related developmental delay, microcephaly, short stature, epilepsy syndrome | Methenyltetrahydrofolate synthetase-related developmental delay, microcephaly, short stature, epilepsy syndrome (disorder) | Methenyltetrahydrofolate synthetase-related developmental delay, microcephaly, short stature, epilepsy syndrome"
+BMGC_DS17738,BMG_DS067910,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 27",,,,,DOID:0111616,autosomal recessive spinocerebellar ataxia 27,C5193058,,618369;618128,MONDO:0032706,"spinocerebellar ataxia, autosomal recessive 27",
+BMGC_DS17739,BMG_DS067911,,TURNPENNY-FRY SYNDROME,,,,,,,C5193060,,618371;600346,MONDO:0032707,turnpenny-fry syndrome,
+BMGC_DS17740,BMG_DS067912,,"CANCER, ALOPECIA, PIGMENT DYSCRASIA, ONYCHODYSTROPHY, AND KERATODERMA",,,,,,,C5193062,,607955;618373,,,
+BMGC_DS17741,BMG_DS067913,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 72,,,,,DOID:0112208,developmental and epileptic encephalopathy 72,C5193063,,618374;601725,MONDO:0032710,"developmental and epileptic encephalopathy, 72",
+BMGC_DS17742,BMG_DS067914,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 38,,,,,DOID:0111466,combined oxidative phosphorylation deficiency 38,C5193064,,611978;618378,MONDO:0032712,combined oxidative phosphorylation deficiency 38,
+BMGC_DS17743,BMG_DS067915,1222659003,RNF13-related severe early-onset epileptic encephalopathy,,,,,,,C5193065,,618379,MONDO:0034106,"developmental and epileptic encephalopathy, 73",Ring finger protein 13-related severe early-onset epileptic encephalopathy | Ring finger protein 13-related severe early-onset epileptic encephalopathy (disorder) | RNF13-related severe early-onset epileptic encephalopathy
+BMGC_DS17744,BMG_DS067916,1304114004,"Facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth syndrome",,,,,,,C5193066,,618381,MONDO:0032714,"facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome","FHEIG (facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth) syndrome | Facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth syndrome (disorder) | FHEIG syndrome | Facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth syndrome"
+BMGC_DS17745,BMG_DS067917,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 69",,,,,DOID:0081230,autosomal recessive intellectual developmental disorder 69,C5193067,,618181;618383,MONDO:0032715,"intellectual developmental disorder, autosomal recessive 69",
+BMGC_DS17746,BMG_DS067918,1340040004,Acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate,,,,,,,C5193068,,618384,MONDO:0032716,"leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate",Acute reversible leukoencephalopathy due to sodium-dependent dicarboxylate transporter deficiency | Acute reversible leucoencephalopathy due to SLC13A3 deficiency | Acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate (disorder) | Acute reversible leukoencephalopathy due to SLC13A3 deficiency | Acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate | Acute reversible leucoencephalopathy due to sodium-dependent dicarboxylate transporter deficiency | Acute reversible leucoencephalopathy with increased urinary alpha-ketoglutarate
+BMGC_DS17747,BMG_DS067919,,"AMELOGENESIS IMPERFECTA, TYPE IIIC",,,,,DOID:0111722,amelogenesis imperfecta type 3C,C5193069,,618386;611211,MONDO:0032717,"amelogenesis imperfecta, type 3C",
+BMGC_DS17748,BMG_DS067920,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY 3",,,,,DOID:0070465,spinocerebellar ataxia with axonal neuropathy type 3,C5193070,,618387;615623,MONDO:0020770,"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3",
+BMGC_DS17749,BMG_DS067921,,"SPONDYLOEPIPHYSEAL DYSPLASIA, KONDO-FU TYPE",,,,,DOID:0112283,spondyloepiphyseal dysplasia Kondo-Fu type,C5193071,,603355;618392,MONDO:0032721,"spondyloepiphyseal dysplasia, kondo-fu type",
+BMGC_DS17750,BMG_DS067922,,IMMUNODEFICIENCY 60 AND AUTOIMMUNITY,,,,,DOID:0111954,immunodeficiency 60,C5193072,,605394;618394,MONDO:0032723,immunodeficiency 60,
+BMGC_DS17751,BMG_DS067923,1286834000,"Spondyloepimetaphyseal dysplasia with joint laxity, EXOC6B type",,,,,,,C5193073,,618395,MONDO:0032724,"spondyloepimetaphyseal dysplasia with joint laxity, type 3","Spondyloepimetaphyseal dysplasia with joint laxity type 3 | Spondyloepimetaphyseal dysplasia with joint laxity exocyst complex component 6B type (disorder) | Spondyloepimetaphyseal dysplasia with joint laxity exocyst complex component 6B type | SEMDJL3 - spondyloepimetaphyseal dysplasia with joint laxity type 3 | Spondyloepimetaphyseal dysplasia with joint laxity, EXOC6B type"
+BMGC_DS17752,BMG_DS067924,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 74,,,,,DOID:0112210,developmental and epileptic encephalopathy 74,C5193074,,618396;137164,MONDO:0032725,"developmental and epileptic encephalopathy, 74",
+BMGC_DS17753,BMG_DS067925,1279845005,Combined oxidative phosphorylation defect type 39,,,,,,,C5193075,,618397,MONDO:0032726,combined oxidative phosphorylation deficiency 39,Combined oxidative phosphorylation defect type 39 | Combined oxidative phosphorylation defect type 39 (disorder) | COXPD39 - combined oxidative phosphorylation defect type 39 | GTP dependent ribosome recycling factor mitochondrial 2-related combined oxidative phosphorylation defect | GFM2-related combined oxidative phosphorylation defect
+BMGC_DS17754,BMG_DS067926,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2EE",,,,,DOID:0111559,Charcot-Marie-Tooth disease type 2EE,C5193076,,137960;618400,MONDO:0032728,"Charcot-Marie-Tooth disease, axonal, type 2EE",
+BMGC_DS17755,BMG_DS067927,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 70",,,,,DOID:0081231,autosomal recessive intellectual developmental disorder 70,C5193077,,618402;613352,MONDO:0032729,"intellectual developmental disorder, autosomal recessive 70",
+BMGC_DS17756,BMG_DS067928,,"LEUKODYSTROPHY, HYPOMYELINATING, 18",,,,,DOID:0070399,hypomyelinating leukodystrophy 18,C5193078,,615843;618404,MONDO:0032730,"leukodystrophy, hypomyelinating, 18",
+BMGC_DS17757,BMG_DS067929,,"DEAFNESS, AUTOSOMAL RECESSIVE 113",,,,,DOID:0111636,autosomal recessive nonsyndromic deafness 113,C5193079,,618410;614591,MONDO:0032732,"hearing loss, autosomal recessive 113",
+BMGC_DS17758,BMG_DS067930,,"GLOBAL DEVELOPMENTAL DELAY, PROGRESSIVE ATAXIA, AND ELEVATED GLUTAMINE",,,,,,,C5193080,,618412;138280,MONDO:0032733,"global developmental delay, progressive ataxia, and elevated glutamine",
+BMGC_DS17759,BMG_DS067931,1255274002,Congenital myopathy with reduced type 2 muscle fibers,,,,,,,C5193081,,618414,MONDO:0034109,congenital myopathy with reduced type 2 muscle fibers,Congenital myopathy with reduced type II muscle fibres | Congenital myopathy with type 2 muscle fibre atrophy | Congenital myopathy with type II fiber atrophy | Congenital myopathy with reduced type II muscle fibers | Congenital myopathy with fast-twitch fiber atrophy | Congenital myopathy with fast-twitch fibre atrophy | Congenital myopathy with reduced type 2 muscle fibers | Congenital myopathy with type II fibre atrophy | Congenital myopathy with reduced type 2 muscle fibers (disorder) | Congenital myopathy with reduced type 2 muscle fibres | Congenital myopathy with type 2 muscle fiber atrophy
+BMGC_DS17760,BMG_DS067932,,CATARACT 48,,,,,DOID:0070354,cataract 48,C5193082,,618415;611282,MONDO:0032735,cataract 48,
+BMGC_DS17761,BMG_DS067933,,"METABOLIC CRISES, RECURRENT, WITH VARIABLE ENCEPHALOMYOPATHIC FEATURES AND NEUROLOGIC REGRESSION",,,,,,,C5193083,,610823;618416,MONDO:0032736,"metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression",
+BMGC_DS17762,BMG_DS067934,,"SPASTIC PARAPLEGIA 80, AUTOSOMAL DOMINANT",,,,,DOID:0112341,hereditary spastic paraplegia 80,C5193084,,609787;618418,MONDO:0032737,"spastic paraplegia 80, autosomal dominant",
+BMGC_DS17763,BMG_DS067935,,MYOECTODERMAL GONADAL DYSGENESIS SYNDROME,,,,,,,C5193085,,618419;600908;615902;618419,MONDO:0032738,"gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy",
+BMGC_DS17764,BMG_DS067936,,SPERMATOGENIC FAILURE 36,,,,,DOID:0111921,spermatogenic failure 36,C5193086,,618420;615902,MONDO:0032739,spermatogenic failure 36,
+BMGC_DS17765,BMG_DS067937,,"DEAFNESS, AUTOSOMAL RECESSIVE 100",,,,,DOID:0111638,autosomal recessive nonsyndromic deafness 100,C5193087,,611648;618422,MONDO:0032740,"hearing loss, autosomal recessive 100",
+BMGC_DS17766,BMG_DS067938,,NEURODEVELOPMENTAL DISORDER WITH IMPAIRED SPEECH AND HYPERKINETIC MOVEMENTS,,,,,,,C5193088,,604083;618425,MONDO:0032741,neurodevelopmental disorder with impaired speech and hyperkinetic movements,
+BMGC_DS17767,BMG_DS067939,,,,,,,,,C5193089,,618426,MONDO:0032742,"encephalopathy, acute, infection-induced, susceptibility to, 9",
+BMGC_DS17768,BMG_DS067940,,SPERMATOGENIC FAILURE 37,,,,,DOID:0111927,spermatogenic failure 37,C5193091,,611430;618429,MONDO:0032744,spermatogenic failure 37,
+BMGC_DS17769,BMG_DS067941,,DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES,,,,,,,C5193092,,618430;603107,MONDO:0032745,developmental delay with variable intellectual impairment and behavioral abnormalities,
+BMGC_DS17770,BMG_DS067942,,"HYDATIDIFORM MOLE, RECURRENT, 3",,,,,,,C5193093,,608797;618431,MONDO:0032746,"hydatidiform mole, recurrent, 3",
+BMGC_DS17771,BMG_DS067943,,"HYDATIDIFORM MOLE, RECURRENT, 4",,,,,,,C5193094,,616109;618432,MONDO:0032747,"hydatidiform mole, recurrent, 4",
+BMGC_DS17772,BMG_DS067944,,SPERMATOGENIC FAILURE 38,,,,,DOID:0111919,spermatogenic failure 38,C5193095,,618424;618433,MONDO:0032748,spermatogenic failure 38,
+BMGC_DS17773,BMG_DS067945,,"DEAFNESS, AUTOSOMAL RECESSIVE 94",,,,,DOID:0111641,autosomal recessive nonsyndromic deafness 94,C5193096,,612803;618434,MONDO:0032749,"hearing loss, autosomal recessive 94",
+BMGC_DS17774,BMG_DS067946,,"ARTHROGRYPOSIS, DISTAL, TYPE 2B2",,,,,DOID:0111601,distal arthrogryposis type 2B2,C5193097,,618435;600692,MONDO:0032750,"arthrogryposis, distal, type 2B2",
+BMGC_DS17775,BMG_DS067947,,"ARTHROGRYPOSIS, DISTAL, TYPE 2B3",,,,,DOID:0111602,distal arthrogryposis type 2B3,C5193098,,618436;160720,MONDO:0032751,"arthrogryposis, distal, type 2B3",
+BMGC_DS17776,BMG_DS067948,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 75,,,,,DOID:0112211,developmental and epileptic encephalopathy 75,C5193099,,612036;618437,MONDO:0032752,"developmental and epileptic encephalopathy, 75",
+BMGC_DS17777,BMG_DS067949,,"SPASTIC ATAXIA 9, AUTOSOMAL RECESSIVE",,,,,,,C5193100,,606988;618438,MONDO:0032753,"spastic ataxia 9, autosomal recessive",
+BMGC_DS17778,BMG_DS067950,1255268002,Oculocerebrodental syndrome,,,,,,,C5193101,,618440,MONDO:0034145,oculocerebrodental syndrome,Oculocerebrodental syndrome | Oculocerebrodental syndrome (disorder) | Oculo-cerebro-dental syndrome
+BMGC_DS17779,BMG_DS067951,,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT VARIABLE BRAIN ABNORMALITIES,,,,,,,C5193102,,618443,MONDO:0032755,neurodevelopmental disorder with or without variable brain abnormalities; NEDBA,
+BMGC_DS17780,BMG_DS067952,,"CILIARY DYSKINESIA, PRIMARY, 41",,,,,DOID:0111858,primary ciliary dyskinesia 41,C5193103,,618449;611398,MONDO:0032757,"ciliary dyskinesia, primary, 41",
+BMGC_DS17781,BMG_DS067953,,"NEURODEGENERATION, EARLY-ONSET, WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA",,,,,,,C5193104,,618451,MONDO:0032758,"neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia",
+BMGC_DS17782,BMG_DS067954,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND VARIABLE SKELETAL ANOMALIES,,,,,,,C5193105,,609225;618453,MONDO:0032759,intellectual developmental disorder with short stature and variable skeletal anomalies,
+BMGC_DS17783,BMG_DS067955,,DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM,,,,,,,C5193106,,618454,MONDO:0032760,developmental delay with or without dysmorphic facies and autism,
+BMGC_DS17784,BMG_DS067956,,"DEAFNESS, AUTOSOMAL RECESSIVE 114",,,,,DOID:0111642,autosomal recessive nonsyndromic deafness 114,C5193107,,618456;604330,MONDO:0032761,"hearing loss, autosomal recessive 114",
+BMGC_DS17785,BMG_DS067957,,"DEAFNESS, AUTOSOMAL RECESSIVE 115",,,,,DOID:0111643,autosomal recessive nonsyndromic deafness 115,C5193108,,612584;618457,MONDO:0032762,"hearing loss, autosomal recessive 115",
+BMGC_DS17786,BMG_DS067958,,IMMUNODEFICIENCY 62,,,,,DOID:0111991,immunodeficiency 62,C5193109,,601855;618459,MONDO:0032763,immunodeficiency 62,
+BMGC_DS17787,BMG_DS067959,,KHAN-KHAN-KATSANIS SYNDROME,,,,,,,C5193110,,608532;618460,MONDO:0032764,Khan-Khan-Katsanis syndrome,
+BMGC_DS17788,BMG_DS067960,,"BLEEDING DISORDER, PLATELET-TYPE, 22",,,,,,,C5193111,,600997;618462,MONDO:0032765,"bleeding disorder, platelet-type, 22",
+BMGC_DS17789,BMG_DS067961,,PHEOCHROMOCYTOMA/PARAGANGLIOMA SYNDROME 6,,,,,,,C5193112,,618464,MONDO:0032767,paragangliomas 6,
+BMGC_DS17790,BMG_DS067962,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 76,,,,,DOID:0112212,developmental and epileptic encephalopathy 76,C5193113,,618468,MONDO:0032768,"developmental and epileptic encephalopathy, 76",
+BMGC_DS17791,BMG_DS067963,,"CONTRACTURES, PTERYGIA, AND SPONDYLOCARPOTARSAL FUSION SYNDROME 1B",,,,,DOID:0081322,"contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B",C5193114,,160720;618469,MONDO:0020746,"contractures, pterygia, and variable skeletal fusions syndrome 1B",
+BMGC_DS17792,BMG_DS067964,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEVERE SPEECH AND AMBULATION DEFECTS,,,,,,,C5193115,,612458;618470,MONDO:0032770,intellectual developmental disorder with severe speech and ambulation defects,
+BMGC_DS17793,BMG_DS067965,,PHEOCHROMOCYTOMA/PARAGANGLIOMA SYNDROME 7,,,,,,,C5193116,,126063;618475,MONDO:0032771,paragangliomas 7,
+BMGC_DS17794,BMG_DS067966,,"BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS",,,,,,,C5193117,,618476;164770,MONDO:0032772,"brain abnormalities, neurodegeneration, and dysosteosclerosis",
+BMGC_DS17795,BMG_DS067967,,"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME",,,,,,,C5193118,,601280;618479,MONDO:0032774,"cerebellar, ocular, craniofacial, and genital syndrome",
+BMGC_DS17796,BMG_DS067968,,NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND SPEECH AND WALKING IMPAIRMENT,,,,,,,C5193119,,600944;618480,MONDO:0032775,neurodevelopmental disorder with seizures and speech and walking impairment,
+BMGC_DS17797,BMG_DS067969,,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 10",,,,,DOID:0111296,generalized epilepsy with febrile seizures plus 10,C5193120,,602780;618482,MONDO:0032777,"generalized epilepsy with febrile seizures plus, type 10",
+BMGC_DS17798,BMG_DS067970,,"ARTHROGRYPOSIS MULTIPLEX CONGENITA 3, MYOGENIC TYPE",,,,,DOID:0080979,arthrogryposis multiplex congenita-3,C5193121,,618484;608441,MONDO:0032778,"arthrogryposis multiplex congenita 3, myogenic type",
+BMGC_DS17799,BMG_DS067971,,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND STRUCTURAL BRAIN ANOMALIES,,,,,,,C5193123,,618492;603331,MONDO:0032779,neurodevelopmental disorder with microcephaly and structural brain anomalies,
+BMGC_DS17800,BMG_DS067972,,"HYPOTONIA, HYPOVENTILATION, IMPAIRED INTELLECTUAL DEVELOPMENT, DYSAUTONOMIA, EPILEPSY, AND EYE ABNORMALITIES",,,,,,,C5193124,,618493,MONDO:0032780,"hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities",
+BMGC_DS17801,BMG_DS067973,,"CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES",,,,,,,C5193125,,618494;607462,MONDO:0032781,"congenital hypotonia, epilepsy, developmental delay, and digital anomalies",
+BMGC_DS17802,BMG_DS067974,,IMMUNODEFICIENCY 63 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY,,,,,DOID:0111997,immunodeficiency 63,C5193126,,146710;618495,MONDO:0032782,immunodeficiency 63 with lymphoproliferation and autoimmunity,
+BMGC_DS17803,BMG_DS067975,,AORTIC VALVE DISEASE 3,,,,,DOID:0080977,aortic valve disease 3,C5193127,,607528;618496,MONDO:0032783,aortic valve disease 3,
+BMGC_DS17804,BMG_DS067976,,NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND NONEPILEPTIC HYPERKINETIC MOVEMENTS,,,,,,,C5193128,,601012;618497,MONDO:0032784,neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements,
+BMGC_DS17805,BMG_DS067977,,"POLYDACTYLY, POSTAXIAL, TYPE A10",,,,,,,C5193129,,617266;618498,MONDO:0032785,"polydactyly, postaxial, type a10",
+BMGC_DS17806,BMG_DS067978,,NOONAN SYNDROME 11,,,,,DOID:0112169,Noonan syndrome 11,C5193130,,618499;608435,MONDO:0032786,Noonan syndrome 11,
+BMGC_DS17807,BMG_DS067979,,HOLOPROSENCEPHALY 12 WITH OR WITHOUT PANCREATIC AGENESIS,,,,,DOID:0081398,holoprosencephaly 12,C5193131,,618500;604917,MONDO:0032787,holoprosencephaly 12 with or without pancreatic agenesis,
+BMGC_DS17808,BMG_DS067980,,CEREBELLAR ATROPHY WITH SEIZURES AND VARIABLE DEVELOPMENTAL DELAY,,,,,,,C5193132,,607082;618501,MONDO:0032788,cerebellar atrophy with seizures and variable developmental delay,
+BMGC_DS17809,BMG_DS067981,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 71",,,,,DOID:0081232,autosomal recessive intellectual developmental disorder 71,C5193133,,613306;618504,MONDO:0032789,"intellectual developmental disorder, autosomal recessive 71",
+BMGC_DS17810,BMG_DS067982,,STOLERMAN NEURODEVELOPMENTAL SYNDROME,,,,,DOID:0081443,Stolerman neurodevelopmental syndrome,C5193134,,618505;611577,MONDO:0032790,neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities,
+BMGC_DS17811,BMG_DS067983,,"NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIC, WITH OPTIC ATROPHY",,,,,,,C5193137,,618511;179020,MONDO:0032792,"neuropathy, hereditary motor and sensory, type VIc, with optic atrophy",
+BMGC_DS17812,BMG_DS067984,,O'Donnell-Luria-Rodan syndrome,,,,,,,C5193138,C000730747,618512,MONDO:0032793,O'Donnell-Luria-Rodan syndrome,
+BMGC_DS17813,BMG_DS067985,,LEBER CONGENITAL AMAUROSIS 19,,,,,DOID:0081169,Leber congenital amaurosis 19,C5193139,,618513;618439,MONDO:0032794,leber congenital amaurosis 19,
+BMGC_DS17814,BMG_DS067986,,"HYPER-IgE SYNDROME 4B, AUTOSOMAL RECESSIVE, WITH RECURRENT INFECTIONS",,,,,DOID:0080596,hyper IgE recurrent infection syndrome 4,C5193141,,600694;618523,MONDO:0032796,"hyper-IgE recurrent infection syndrome 4, autosomal recessive",
+BMGC_DS17815,BMG_DS067987,,MITOCHONDRIAL DNA DEPLETION SYNDROME 16 (HEPATIC TYPE),,,,,DOID:0070446,mitochondrial DNA depletion syndrome 16,C5193142,,618528,MONDO:0032799,mitochondrial DNA depletion syndrome 16 (hepatic type),
+BMGC_DS17816,BMG_DS067988,,"ROBINOW SYNDROME, AUTOSOMAL RECESSIVE 2",,,,,DOID:0060974,autosomal recessive Robinow syndrome 2,C5193143,,618529;612895,MONDO:0032800,"robinow syndrome, autosomal recessive 2",
+BMGC_DS17817,BMG_DS067989,,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 6,,,,,DOID:0080766,erythrokeratodermia variabilis et progressiva 6,C5193144,,618531;606936,MONDO:0032801,erythrokeratodermia variabilis et progressiva 6,
+BMGC_DS17818,BMG_DS067990,,"ECTODERMAL DYSPLASIA 15, HYPOHIDROTIC/HAIR TYPE",,,,,DOID:0111651,ectodermal dysplasia 15,C5193145,,601891;618535,MONDO:0032804,"ectodermal dysplasia 15, hypohidrotic/hair type",
+BMGC_DS17819,BMG_DS067991,,SHUKLA-VERNON SYNDROME,,,,,DOID:0111841,Shukla-Vernon syndrome,C5193146,,300688;301029,MONDO:0026727,Shukla-Vernon syndrome,
+BMGC_DS17820,BMG_DS067992,,"ICHTHYOTIC KERATODERMA, SPASTICITY, HYPOMYELINATION, AND DYSMORPHIC FACIAL FEATURES",,,,,,,C5193147,,618527;611813,MONDO:0032798,"ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features",
+BMGC_DS17821,BMG_DS067993,,MICROPHTHALMIA AND/OR COLOBOMA WITH DEVELOPMENTAL DELAY,,,,,,,C5193150,,615145,,,
+BMGC_DS17822,BMG_DS068002,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 59",,,,,,,C5193190,,618522;602123,MONDO:0032795,intellectual developmental disorder 59,
+BMGC_DS17823,BMG_DS068011,,"MITOCHONDRIAL MYOPATHY, EPISODIC, WITHOUT OPTIC ATROPHY AND REVERSIBLE LEUKOENCEPHALOPATHY",,,,,,,C5193222,,614585,,,
+BMGC_DS17824,BMG_DS068012,,"MITOCHONDRIAL MYOPATHY, EPISODIC, WITH OPTIC ATROPHY AND REVERSIBLE LEUKOENCEPHALOPATHY",,,,,,,C5193223,,251900;614585,MONDO:0020714,"mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy",
+BMGC_DS17825,BMG_DS068016,,"HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHISM",,,,,,,C5193233,,613124,MONDO:0013149,"hydrops fetalis, nonimmune, with gracile bones and dysmorphic features",
+BMGC_DS17826,BMG_DS068021,267553005;154787005;234349007,Microcytic anemia,,,,,,,C5194182,,MTHU006439,MONDO:0001245,microcytic anemia,(Anaemia: [iron deficiency] or [microcytic]) or (Kelly-Paterson syndrome) or (Plummer-Vinson syndrome) | Anemia - iron defic. | Iron deficiency anemia | Iron deficiency anemias | Microcytic anemia | Kelly-Paterson syndrome | Plummer-Vinson syndrome | Plummer-Vinson syndr. | Kelly-Paterson synd. | Iron deficiency anaemias | Iron deficiency anaemia | Microcytic anaemia | Anaemia - iron defic. | (Anemia: [iron deficiency] or [microcytic]) or (Kelly-Paterson syndrome) or (Plummer-Vinson syndrome) | (Anaemia: [iron deficiency] or [microcytic]) or (Kelly-Paterson syndrome) or (Plummer-Vinson syndrome) (disorder) | (Anaemia: [iron deficiency] or [microcytic]) or (Kelly-Paterson syndrome) or (Plummer-Vinson syndrome) | (Anemia: [iron deficiency] or [microcytic]) or (Kelly-Paterson syndrome) or (Plummer-Vinson syndrome) | Kelly-Paterson syndrome | Plummer-Vinson syndrome | Plummer-Vinson syndr. | Kelly-Paterson synd. | Anemia - iron defic. | Microcytic anemia | Iron deficiency anemias | Iron deficiency anemia | Microcytic anaemia | Iron deficiency anaemias | Anaemia - iron defic. | Iron deficiency anaemia | (Anaemia: [iron deficiency] or [microcytic]) or (Kelly-Paterson syndrome) or (Plummer-Vinson syndrome) (disorder) | Microcytic anemia | Microcytic anaemia | Microcytic anemia (disorder)
+BMGC_DS17827,BMG_DS068044,,X-Linked Familial Exudative Vitreoretinopathy,Familial Exudative Vitreoretinopathies,,,,,,C5197731,D000080345,,,,
+BMGC_DS17828,BMG_DS068047,,Inherited Immunodeficiency Diseases,Primary Immunodeficiency Diseases,,,,,,C5197805,D000081207,,,,
+BMGC_DS17829,BMG_DS068050,,Evaporative Dry Eye Disease,Dry Eye Syndromes,,,,,,C5197850,D015352,,,,
+BMGC_DS17830,BMG_DS068054,,Adenylosuccinate lyase deficiency type 4,,,,,,,C5200299,C538235,,,,
+BMGC_DS17831,BMG_DS068055,,Adenylosuccinate lyase deficiency type 3,,,,,,,C5200300,C538235,,,,
+BMGC_DS17832,BMG_DS068056,,Adenylosuccinate lyase deficiency type 2,,,,,,,C5200301,C538235,,,,
+BMGC_DS17833,BMG_DS068057,,Adenylosuccinate lyase deficiency type 1,,,,,,,C5200302,C538235,,,,
+BMGC_DS17834,BMG_DS068058,890233009,Autosomal dominant Robinow syndrome,,,,,,,C5200540,,,MONDO:0008389,autosomal dominant Robinow syndrome,Autosomal dominant Robinow syndrome (disorder) | Autosomal dominant Robinow syndrome
+BMGC_DS17835,BMG_DS068065,,Pes Anserine Bursitis,Bursitis,,,,,,C5200782,D002062,,,,
+BMGC_DS17836,BMG_DS068069,,"SHORT SLEEP, FAMILIAL NATURAL, 1",,,,,,,C5200932,,606200;612975,,,
+BMGC_DS17837,BMG_DS068070,,Giant Axonal Neuropathy,Giant Axonal Neuropathy,,,,DOID:0090068,giant axonal neuropathy 1,C5200933,D056768,,MONDO:0000128,giant axonal neuropathy,
+BMGC_DS17838,BMG_DS068071,,,,,,,,,C5200934,,155100;153640;605249;600208,MONDO:0015912,macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss,
+BMGC_DS17839,BMG_DS068078,789675009,Complete achromatopsia,,,,,,,C5201048,,MTHU013744,,,Complete achromatopsia | Complete color blindness | Complete colour blindness | Complete achromatopsia (disorder) | Total colour blindness | Rod monochromatism | Total color blindness
+BMGC_DS17840,BMG_DS068080,,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 1,,,,,,,C5201145,,610273;610293,MONDO:0012465,hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency,
+BMGC_DS17841,BMG_DS068081,818950005,Blau syndrome,,,,M04.8,,,C5201146,,186580;609464,MONDO:0008523,Blau syndrome,Blau syndrome | Blau syndrome (disorder)
+BMGC_DS17842,BMG_DS068084,,"HYPOPIGMENTATION, ORGANOMEGALY, AND DELAYED MYELINATION AND DEVELOPMENT",,,,,,,C5203300,,618541;602727,MONDO:0032805,"hypopigmentation, organomegaly, and delayed myelination and development",
+BMGC_DS17843,BMG_DS068085,,"MYOPATHY, DISTAL, 6, ADULT-ONSET, AUTOSOMAL DOMINANT",,,,,,,C5203349,,102573;618655,MONDO:0032853,"myopathy, distal, 6, adult-onset, autosomal dominant",
+BMGC_DS17844,BMG_DS068086,,"ROTHMUND-THOMSON SYNDROME, TYPE 2",,,,,,,C5203410,,268400;603780,MONDO:0016369,Rothmund-Thomson syndrome type 2,
+BMGC_DS17845,BMG_DS068087,,"NEUTROPENIA, SEVERE CONGENITAL, 8, AUTOSOMAL DOMINANT",,,,,DOID:0112135,severe congenital neutropenia 8,C5203411,,604857;618752,MONDO:0032899,"neutropenia, severe congenital, 8, autosomal dominant",
+BMGC_DS17846,BMG_DS068088,,COVID-19 Virus Disease,COVID-19,,,,DOID:0080600,COVID-19,C5203670,D000086382,,MONDO:0100096,COVID-19,
+BMGC_DS17847,BMG_DS068089,789160000,Focal facial dermal dysplasia type III,,,,,,,C5203693,,,,,Setleis syndrome | Focal facial dermal dysplasia 3 Setleis type | Focal facial dermal dysplasia type III | Focal facial dermal dysplasia type III (disorder) | FFDD type 3 - focal facial dermal dysplasia type 3
+BMGC_DS17848,BMG_DS068188,788584007,"Blepharophimosis, intellectual disability syndrome",,,,,,,C5229849,,,MONDO:0017393,blepharophimosis - intellectual disability syndrome,"Blepharophimosis, intellectual disability syndrome (disorder) | Blepharophimosis, intellectual disability syndrome"
+BMGC_DS17849,BMG_DS068269,789063000,"Primary hyperaldosteronism, seizures, neurological abnormalities syndrome",,,,,,,C5230308,,,,,"Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (disorder) | Primary hyperaldosteronism, seizures, neurological abnormalities syndrome"
+BMGC_DS17850,BMG_DS068303,789657008,ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis,,,,,,,C5230619,,,,,"ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis | Juvenile parkinsonism, neuronal ceroid lipofuscinosis | ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis (disorder) | CLN12 disease"
+BMGC_DS17851,BMG_DS068334,818959006,Trichorhinophalangeal syndrome type 1 and 3,,,,,,,C5231006,,,,,Trichorhinophalangeal syndrome type 1 and 3 | Trichorhinophalangeal syndrome type 1 and 3 (disorder) | Trichorhinophalangeal syndrome type I and III
+BMGC_DS17852,BMG_DS068336,,,,,,,,,C5231010,,,MONDO:0019848,posterior hypospadias,
+BMGC_DS17853,BMG_DS068339,819950002,Generalized glucocorticoid resistance syndrome,,,,,,,C5231034,,,,,Generalized glucocorticoid resistance syndrome (disorder) | Generalized glucocorticoid resistance syndrome | Generalised glucocorticoid resistance syndrome
+BMGC_DS17854,BMG_DS068347,827050005,Palsy of glossopharyngeal nerve,,,,,DOID:3816,glossopharyngeal nerve paralysis,C5231192,,,MONDO:0002781,glossopharyngeal nerve paralysis,Palsy of glossopharyngeal nerve | Palsy of glossopharyngeal nerve (disorder) | Ninth cranial nerve palsy
+BMGC_DS17855,BMG_DS068349,827115000,Autosomal dominant progressive external ophthalmoplegia,,,,,,,C5231255,,,MONDO:0008003,autosomal dominant progressive external ophthalmoplegia,Autosomal dominant progressive external ophthalmoplegia (disorder) | Autosomal dominant progressive external ophthalmoplegia | adPEO - autosomal dominant progressive external ophthalmoplegia
+BMGC_DS17856,BMG_DS068351,827172005,X-linked progressive cerebellar ataxia,,,,,,,C5231313,,,,,X-linked progressive cerebellar ataxia | X-linked progressive cerebellar ataxia (disorder)
+BMGC_DS17857,BMG_DS068353,,OCULOPHARYNGODISTAL MYOPATHY 1,,,,,DOID:0081297,oculopharyngodistal myopathy 1,C5231388,,164310;618299,MONDO:0020793,oculopharyngodistal myopathy 1,
+BMGC_DS17858,BMG_DS068354,,"BLADDER DYSFUNCTION, AUTONOMIC, WITH IMPAIRED PUPILLARY REFLEX AND SECONDARY CAKUT",,,,,,,C5231389,,118503;191800,MONDO:0008630,"urinary bladder, atony of",
+BMGC_DS17859,BMG_DS068355,,"CEREBELLAR HYPOPLASIA/ATROPHY, EPILEPSY, AND GLOBAL DEVELOPMENTAL DELAY",,,,,DOID:0070339,"cerebellar hyplasia/atrophy, epilepsy, and global developmental delay",C5231391,,605609;213000,MONDO:0008939,isolated cerebellar hypoplasia/agenesis,
+BMGC_DS17860,BMG_DS068356,,"HYDROCEPHALUS, NORMAL-PRESSURE, 1",,,,,,,C5231392,,236690,,,
+BMGC_DS17861,BMG_DS068357,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Icc",,,,,DOID:0111839,congenital disorder of glycosylation Icc,C5231393,,300715;301031,MONDO:0026729,"congenital disorder of glycosylation, type ICC",
+BMGC_DS17862,BMG_DS068358,,BASILICATA-AKHTAR SYNDROME,,,,,DOID:0111838,Basilicata-Akhtar syndrome,C5231394,,300609;301032,MONDO:0026730,Basilicata-Akhtar syndrome,
+BMGC_DS17863,BMG_DS068359,,"HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 8",,,,,DOID:0111837,congenital nongoitrous hypothyroidism 8,C5231395,,301033;300196,MONDO:0026731,"hypothyroidism, congenital, nongoitrous, 8",
+BMGC_DS17864,BMG_DS068360,,"HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 9",,,,,DOID:0111835,congenital nongoitrous hypothyroidism 9,C5231396,,301035;300904,MONDO:0026732,"hypothyroidism, congenital, nongoitrous, 9",
+BMGC_DS17865,BMG_DS068361,,"CHOLESTASIS, LOW GGT, ACUTE LIVER FAILURE, AND NEURODEGENERATION SYNDROME",,,,,DOID:0111155,autosomal recessive spinocerebellar ataxia 21,C5231399,,607982;616719,,,
+BMGC_DS17866,BMG_DS068362,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 61",,,,,,,C5231400,,603808;618009,MONDO:0032485,intellectual developmental disorder 61,
+BMGC_DS17867,BMG_DS068363,,CONGENITAL MYOPATHY 16,,,,,DOID:0081348,congenital myopathy 16,C5231401,,160794;618524,MONDO:0032797,"myopathy, congenital, with tremor",
+BMGC_DS17868,BMG_DS068364,,IMMUNODEFICIENCY 64 WITH LYMPHOPROLIFERATION,,,,,DOID:0111980,immunodeficiency 64,C5231402,,618534;603962,MONDO:0032803,immunodeficiency 64,
+BMGC_DS17869,BMG_DS068365,,"TRICHOTHIODYSTROPHY 7, NONPHOTOSENSITIVE",,,,,DOID:0111870,nonphotosensitive trichothiodystrophy 7,C5231403,,187790;618546,MONDO:0032806,"trichothiodystrophy 7, nonphotosensitive",
+BMGC_DS17870,BMG_DS068366,,NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES,,,,,,,C5231404,,618547;142600,MONDO:0032807,neurodevelopmental disorder with visual defects and brain anomalies,
+BMGC_DS17871,BMG_DS068367,,MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 4,,,,,DOID:0112213,multiple congenital anomalies-hypotonia-seizures syndrome 4,C5231405,,618548;605754,MONDO:0032808,"developmental and epileptic encephalopathy, 77",
+BMGC_DS17872,BMG_DS068368,,,,,,,,,C5231406,,618549,MONDO:0032809,"hepatitis, fulminant viral, susceptibility to",
+BMGC_DS17873,BMG_DS068369,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 7,,,,,,,C5231407,,608420;618550,MONDO:0032810,oocyte maturation defect 7,
+BMGC_DS17874,BMG_DS068370,,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE1I",,,,,,,C5231408,,618555,MONDO:0032811,"night blindness, congenital stationary, type1i",
+BMGC_DS17875,BMG_DS068371,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 78,,,,,DOID:0112214,developmental and epileptic encephalopathy 78,C5231409,,137140;618557,MONDO:0032812,"developmental and epileptic encephalopathy, 78",
+BMGC_DS17876,BMG_DS068372,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 79,,,,,DOID:0112215,developmental and epileptic encephalopathy 79,C5231410,,137142;618559,MONDO:0032813,"developmental and epileptic encephalopathy, 79",
+BMGC_DS17877,BMG_DS068373,1173997008,Pontine autosomal dominant microangiopathy with leukoencephalopathy,,,,,,,C5231411,,618564,MONDO:0032814,"microangiopathy and leukoencephalopathy, pontine, autosomal dominant",Pontine autosomal dominant microangiopathy with leukoencephalopathy (disorder) | Pontine autosomal dominant microangiopathy with leukoencephalopathy | Pontine autosomal dominant microangiopathy with leucoencephalopathy | PADMAL - pontine autosomal dominant microangiopathy with leukoencephalopathy | PADMAL - pontine autosomal dominant microangiopathy with leucoencephalopathy
+BMGC_DS17878,BMG_DS068374,,MITOCHONDRIAL DNA DEPLETION SYNDROME 17,,,,,DOID:0070448,mitochondrial DNA depletion syndrome 17,C5231412,,618567;606906,MONDO:0032815,mitochondrial DNA depletion syndrome 17,
+BMGC_DS17879,BMG_DS068375,,"NEURODEVELOPMENTAL DISORDER WITH ATAXIA, HYPOTONIA, AND MICROCEPHALY",,,,,,,C5231413,,617853;618569,MONDO:0032816,"neurodevelopmental disorder with ataxia, hypotonia, and microcephaly",
+BMGC_DS17880,BMG_DS068376,,"NEURODEVELOPMENTAL DISORDER WITH CATARACTS, POOR GROWTH, AND DYSMORPHIC FACIES",,,,,DOID:0070346,"neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies",C5231414,,611345;618571,MONDO:0032817,"neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies",
+BMGC_DS17881,BMG_DS068377,,NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR HYPOPLASIA AND SPASTICITY,,,,,,,C5231415,,611351;618572,MONDO:0032818,neurodevelopmental disorder with cerebellar hypoplasia and spasticity,
+BMGC_DS17882,BMG_DS068378,,NEURODEVELOPMENTAL DISORDER WITH STRUCTURAL BRAIN ANOMALIES AND DYSMORPHIC FACIES,,,,,,,C5231416,,602050;618577,MONDO:0032820,neurodevelopmental disorder with structural brain anomalies and dysmorphic facies,
+BMGC_DS17883,BMG_DS068379,,CONGENITAL MYOPATHY 19,,,,,DOID:0081351,congenital myopathy 19,C5231417,,618578;167410,MONDO:0032821,"myopathy, congenital, progressive, with scoliosis",
+BMGC_DS17884,BMG_DS068380,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 80,,,,,DOID:0112216,developmental and epileptic encephalopathy 80,C5231418,,604122;618580,MONDO:0032822,"developmental and epileptic encephalopathy, 80",
+BMGC_DS17885,BMG_DS068381,,"NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES, SEIZURES, AND SCOLIOSIS",,,,,,,C5231419,,618590;608528,MONDO:0032824,glycosylphosphatidylinositol biosynthesis defect 21,
+BMGC_DS17886,BMG_DS068382,,"SHORT SLEEP, FAMILIAL NATURAL, 2",,,,,,,C5231420,,618591;109630,,,
+BMGC_DS17887,BMG_DS068383,,,,,,,,,C5231421,,618596,MONDO:0032827,"epilepsy, idiopathic generalized, susceptibility to, 16",
+BMGC_DS17888,BMG_DS068384,,"SPASTIC TETRAPLEGIA AND AXIAL HYPOTONIA, PROGRESSIVE",,,,,,,C5231422,,147450;618598,MONDO:0032828,"spastic tetraplegia and axial hypotonia, progressive",
+BMGC_DS17889,BMG_DS068385,,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES,,,,,,,C5231423,,180660;618603,MONDO:0032829,neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities,
+BMGC_DS17890,BMG_DS068386,,SNIJDERS BLOK-FISHER SYNDROME,,,,,,,C5231424,,602480;618604,MONDO:0032830,snijders blok-fisher syndrome,
+BMGC_DS17891,BMG_DS068387,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 13",,,,,DOID:0112332,pontocerebellar hypoplasia type 13,C5231425,,618606;615738,MONDO:0032831,"pontocerebellar hypoplasia, type 13",
+BMGC_DS17892,BMG_DS068388,,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH NASAL SPEECH, DYSMORPHIC FACIES, AND VARIABLE SKELETAL ANOMALIES",,,,,,,C5231426,,618608;604909,MONDO:0032832,"intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies",
+BMGC_DS17893,BMG_DS068389,,"LOWER URINARY TRACT OBSTRUCTION, CONGENITAL",,,,,,,C5231427,,608669;618612,MONDO:0032833,"lower urinary tract obstruction, congenital",
+BMGC_DS17894,BMG_DS068390,,RETINITIS PIGMENTOSA 86,,,,,DOID:0112143,retinitis pigmentosa 86,C5231428,,613344;618613,MONDO:0032834,retinitis pigmentosa 86,
+BMGC_DS17895,BMG_DS068391,,,,,,,,,C5231429,,618619,MONDO:0032836,Weiss-Kruszka syndrome,
+BMGC_DS17896,BMG_DS068392,,ABDOMINAL OBESITY-METABOLIC SYNDROME 4,,,,,DOID:0080945,abdominal obesity-metabolic syndrome 4,C5231430,,618620;609443,MONDO:0032837,abdominal obesity-metabolic syndrome 4,
+BMGC_DS17897,BMG_DS068393,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES",,,,,,,C5231431,,610457;618622,MONDO:0032838,"neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies",
+BMGC_DS17898,BMG_DS068394,,NOONAN SYNDROME 12,,,,,DOID:0112170,Noonan syndrome 12,C5231432,,618624;600098,MONDO:0032839,noonan syndrome 12,
+BMGC_DS17899,BMG_DS068395,1003922004,Rothmund Thomson syndrome type 1,,,,,,,C5231433,,618625,MONDO:0016368,Rothmund-Thomson syndrome type 1,Rothmund Thomson syndrome type 1 (disorder) | Rothmund Thomson syndrome type 1
+BMGC_DS17900,BMG_DS068396,,"USHER SYNDROME, TYPE 1M",,,,,,,C5231434,,618632;606351,MONDO:0032841,"Usher syndrome, type 1M",
+BMGC_DS17901,BMG_DS068397,,SIDDIQI SYNDROME,,,,,DOID:0081273,Siddiqi syndrome,C5231435,,612029;618635,MONDO:0032842,Siddiqi syndrome,
+BMGC_DS17902,BMG_DS068398,,OCULOPHARYNGEAL MYOPATHY WITH LEUKOENCEPHALOPATHY 1,,,,,,,C5231436,,618639;618637,MONDO:0032843,oculopharyngeal myopathy with leukoencephalopathy 1,
+BMGC_DS17903,BMG_DS068399,,INFANTILE LIVER FAILURE SYNDROME 3,,,,,,,C5231437,,610089;618641,MONDO:0032844,infantile liver failure syndrome 3,
+BMGC_DS17904,BMG_DS068400,,SPERMATOGENIC FAILURE 39,,,,,DOID:0111926,spermatogenic failure 39,C5231438,,618643;610063,MONDO:0032845,spermatogenic failure 39,
+BMGC_DS17905,BMG_DS068401,,"OSTEOGENESIS IMPERFECTA, TYPE XX",,,,,DOID:0111849,osteogenesis imperfecta type 20,C5231439,,607783;618644,MONDO:0032846,"osteogenesis imperfecta, type 20",
+BMGC_DS17906,BMG_DS068402,,DIENCEPHALIC-MESENCEPHALIC JUNCTION DYSPLASIA SYNDROME 2,,,,,,,C5231440,,616253;618646,MONDO:0020762,diencephalic-mesencephalic junction dysplasia syndrome 2,
+BMGC_DS17907,BMG_DS068403,,"IMMUNODEFICIENCY 65, SUSCEPTIBILITY TO VIRAL INFECTIONS",,,,,DOID:0111978,immunodeficiency 65,C5231441,,618648;147574,MONDO:0032848,"immunodeficiency 65, susceptibility to viral infections",
+BMGC_DS17908,BMG_DS068404,,HALPERIN-BIRK SYNDROME,,,,,DOID:0070539,Halperin-Birk syndrome,C5231442,,618651;610257,MONDO:0032849,"neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies",
+BMGC_DS17909,BMG_DS068405,,NEUROOCULOCARDIOGENITOURINARY SYNDROME,,,,,DOID:0111675,neurooculocardiogenitourinary syndrome,C5231443,,618586;618652,MONDO:0032850,neurooculocardiogenitourinary syndrome,
+BMGC_DS17910,BMG_DS068406,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND DYSMORPHIC FACIES,,,,,,,C5231444,,600326;618653,MONDO:0032851,intellectual developmental disorder with impaired language and dysmorphic facies,
+BMGC_DS17911,BMG_DS068407,,CONGENITAL MYOPATHY 8,,,,,DOID:0081342,congenital myopathy 8,C5231445,,618654;102573,MONDO:0032852,"myopathy, congenital, with structured cores and z-line abnormalities",
+BMGC_DS17912,BMG_DS068408,,ZIMMERMANN-LABAND SYNDROME 3,,,,,,,C5231447,,618658;602983,MONDO:0032854,zimmermann-laband syndrome 3,
+BMGC_DS17913,BMG_DS068409,,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES,,,,,,,C5231448,,607159;618659,MONDO:0032855,neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies,
+BMGC_DS17914,BMG_DS068410,,"DIARRHEA 11, MALABSORPTIVE, CONGENITAL",,,,,,,C5231449,,618656;618662,MONDO:0032857,"diarrhea 11, malabsorptive, congenital",
+BMGC_DS17915,BMG_DS068411,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 81,,,,,DOID:0112217,developmental and epileptic encephalopathy 81,C5231450,,618663;612186,MONDO:0032858,"developmental and epileptic encephalopathy, 81",
+BMGC_DS17916,BMG_DS068412,,SPERMATOGENIC FAILURE 40,,,,,DOID:0111918,spermatogenic failure 40,C5231451,,614270;618664,MONDO:0032859,spermatogenic failure 40,
+BMGC_DS17917,BMG_DS068413,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 72",,,,,DOID:0080765,autosomal recessive intellectual developmental disorder 72,C5231452,,618628;618665,MONDO:0032860,"intellectual developmental disorder, autosomal recessive 72",
+BMGC_DS17918,BMG_DS068414,,SITOSTEROLEMIA 2,,,,,DOID:0060983,sitosterolemia 2,C5231453,,605459;618666,MONDO:0020748,sitosterolemia 2,
+BMGC_DS17919,BMG_DS068415,,"HYDROCEPHALUS, CONGENITAL, 4",,,,,,,C5231454,,618667;618570,MONDO:0032862,"hydrocephalus, congenital communicating, 1",
+BMGC_DS17920,BMG_DS068416,,SPERMATOGENIC FAILURE 41,,,,,DOID:0111912,spermatogenic failure 41,C5231455,,618661;618670,MONDO:0032863,spermatogenic failure 41,
+BMGC_DS17921,BMG_DS068417,,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES",,,,,,,C5231456,,604910;618672,MONDO:0032864,"intellectual developmental disorder with speech delay, autism, and dysmorphic facies",
+BMGC_DS17922,BMG_DS068418,,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 5",,,,,,,C5231457,,618674;616381,MONDO:0032865,"pulmonary fibrosis and/or bone marrow failure, telomere-related, 5",
+BMGC_DS17923,BMG_DS068419,,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 10",,,,,,,C5231458,,612034;618677,MONDO:0032866,"cortical dysplasia, complex, with other brain malformations 10",
+BMGC_DS17924,BMG_DS068420,,,,,,,,,C5231459,,618680,MONDO:0032867,"pancreatic cancer, susceptibility to, 5",
+BMGC_DS17925,BMG_DS068421,,LESSEL-KUBISCH SYNDROME,,,,,,,C5231460,,618681;164785,MONDO:0032868,lessel-kubisch syndrome,
+BMGC_DS17926,BMG_DS068422,,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 6",,,,,DOID:0111749,mitochondrial complex V (ATP synthase) deficiency nuclear type 6,C5231461,,618683;615204,MONDO:0032869,"mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6",
+BMGC_DS17927,BMG_DS068423,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND BEHAVIORAL ABNORMALITIES,,,,,DOID:0111674,intellectual developmental disorder with short stature and behavioral abnormalities,C5231462,,610166;618687,MONDO:0032870,intellectual developmental disorder with short stature and behavioral abnormalities,
+BMGC_DS17928,BMG_DS068424,,"LEUKODYSTROPHY, HYPOMYELINATING, 19, TRANSIENT INFANTILE",,,,,DOID:0070400,hypomyelinating leukodystrophy 19,C5231463,,618688;618685,MONDO:0032871,"leukodystrophy, hypomyelinating, 19, transient infantile",
+BMGC_DS17929,BMG_DS068425,,,,,,,,,C5231464,,618695,MONDO:0032872,"ciliary dyskinesia, primary, 42",
+BMGC_DS17930,BMG_DS068426,,RETINITIS PIGMENTOSA 87 WITH CHOROIDAL INVOLVEMENT,,,,,DOID:0112144,retinitis pigmentosa 87,C5231465,,180069;618697,MONDO:0032873,retinitis pigmentosa 87 with choroidal involvement,
+BMGC_DS17931,BMG_DS068427,,"CILIARY DYSKINESIA, PRIMARY, 43",,,,,DOID:0111856,primary ciliary dyskinesia 43,C5231466,,618699,MONDO:0032874,"ciliary dyskinesia, primary, 43",
+BMGC_DS17932,BMG_DS068428,,SHORT STATURE AND MICROCEPHALY WITH GENITAL ANOMALIES,,,,,,,C5231467,,611510;618702,MONDO:0032875,short stature and microcephaly with genital anomalies,
+BMGC_DS17933,BMG_DS068429,,NEURODEVELOPMENTAL DISORDER WITH ABSENT LANGUAGE AND VARIABLE SEIZURES,,,,,,,C5231469,,618707;605035,MONDO:0032876,neurodevelopmental disorder with absent language and variable seizures,
+BMGC_DS17934,BMG_DS068430,,NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES,,,,,,,C5231470,,606582;618709,MONDO:0032877,neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures,
+BMGC_DS17935,BMG_DS068431,,"NEURODEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES, ABSENT SPEECH, AND HYPOTONIA",,,,,,,C5231471,,618689;618718,MONDO:0032878,"neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia",
+BMGC_DS17936,BMG_DS068432,,,,,,,,,C5231472,,618719,MONDO:0032879,"megabladder, congenital",
+BMGC_DS17937,BMG_DS068433,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 82,,,,,DOID:0080715,developmental and epileptic encephalopathy 82,C5231473,,138150;618721,MONDO:0032880,"developmental and epileptic encephalopathy, 82",
+BMGC_DS17938,BMG_DS068434,,PREMATURE OVARIAN FAILURE 16,,,,,DOID:0080873,primary ovarian insufficiency 16,C5231474,,601930;618723,MONDO:0032881,premature ovarian failure 16,
+BMGC_DS17939,BMG_DS068435,,HEYN-SPROUL-JACKSON SYNDROME,,,,,,,C5231475,,618724;602769,MONDO:0032882,Heyn-Sproul-Jackson syndrome,
+BMGC_DS17940,BMG_DS068436,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT SEIZURES,,,,,,,C5231476,,618725;608325,MONDO:0032883,intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures,
+BMGC_DS17941,BMG_DS068437,,"ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES",,,,,,,C5231477,,618727,MONDO:0032884,"ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies",
+BMGC_DS17942,BMG_DS068438,,"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, ISIDOR-TOUTAIN TYPE",,,,,,,C5231478,,618728;113703,MONDO:0032885,"spondyloepimetaphyseal dysplasia, Isidor-Toutain type",
+BMGC_DS17943,BMG_DS068439,,LIANG-WANG SYNDROME,,,,,,,C5231479,,600150;618729,MONDO:0032886,Liang-Wang syndrome,
+BMGC_DS17944,BMG_DS068440,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CORTICAL MALFORMATIONS, AND SPASTICITY",,,,,,,C5231480,,616715;618730,MONDO:0032887,"neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity",
+BMGC_DS17945,BMG_DS068441,,NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES AND WITH OR WITHOUT VERTEBRAL OR CARDIAC ANOMALIES,,,,,,,C5231481,,618731,MONDO:0032888,neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies,
+BMGC_DS17946,BMG_DS068442,,,,,,,,,C5231482,,618732,MONDO:0032889,Poirier-Bienvenu neurodevelopmental syndrome,
+BMGC_DS17947,BMG_DS068443,,NEUROMUSCULAR OCULOAUDITORY SYNDROME,,,,,,,C5231483,,603405;618733,MONDO:0032890,neuromuscular disease and ocular or auditory anomalies with or without seizures,
+BMGC_DS17948,BMG_DS068444,,"ANEURYSM, INTRACRANIAL BERRY, 12",,,,,DOID:0080975,intracranial berry aneurysm 12,C5231484,,618734;616821,MONDO:0032891,"aneurysm, intracranial berry, 12",
+BMGC_DS17949,BMG_DS068445,,STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS,,,,,,,C5231485,,618736;600470,MONDO:0032892,structural brain anomalies with impaired intellectual development and craniosynostosis,
+BMGC_DS17950,BMG_DS068446,,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 15",,,,,DOID:0081266,"pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures",C5231486,,618737;617817,MONDO:0032893,"pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures",
+BMGC_DS17951,BMG_DS068447,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 83,,,,,DOID:0112218,developmental and epileptic encephalopathy 83,C5231487,,191760;618744,MONDO:0032895,"developmental and epileptic encephalopathy, 83",
+BMGC_DS17952,BMG_DS068448,,SPERMATOGENIC FAILURE 42,,,,,DOID:0111923,spermatogenic failure 42,C5231488,,618745;618735,MONDO:0032896,spermatogenic failure 42,
+BMGC_DS17953,BMG_DS068449,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES,,,,,,,C5231489,,603184;618748,MONDO:0032897,intellectual developmental disorder with hypotonia and behavioral abnormalities,
+BMGC_DS17954,BMG_DS068450,,SPERMATOGENIC FAILURE 43,,,,,DOID:0111917,spermatogenic failure 43,C5231490,,618751;610172,MONDO:0032898,spermatogenic failure 43,
+BMGC_DS17955,BMG_DS068451,,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS,,,,,,,C5231491,,618760,MONDO:0032900,neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements,
+BMGC_DS17956,BMG_DS068452,,CATIFA SYNDROME,,,,,,,C5231492,,618761;610354,MONDO:0032901,Catifa syndrome,
+BMGC_DS17957,BMG_DS068453,,JOUBERT SYNDROME 36,,,,,,,C5231493,,618763;618413,MONDO:0032902,Joubert syndrome 36,
+BMGC_DS17958,BMG_DS068454,,"ARTHROGRYPOSIS MULTIPLEX CONGENITA 4, NEUROGENIC, WITH AGENESIS OF THE CORPUS CALLOSUM",,,,,DOID:0080980,arthrogryposis multiplex congenita-4,C5231494,,618766;616365,MONDO:0032903,"arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum",
+BMGC_DS17959,BMG_DS068455,,"CORNEAL DYSTROPHY, MEESMANN, 2",,,,,DOID:0080671,Meesmann corneal dystrophy 2,C5231495,,618767;148043,MONDO:0032904,"corneal dystrophy, Meesmann, 2",
+BMGC_DS17960,BMG_DS068456,,LYMPHATIC MALFORMATION 8,,,,,,,C5231496,,114190;618773,MONDO:0032907,lymphatic malformation 8,
+BMGC_DS17961,BMG_DS068457,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 60, WITH SEIZURES",,,,,,,C5231497,,618587;601024,MONDO:0032823,intellectual developmental disorder 60 with seizures,
+BMGC_DS17962,BMG_DS068458,,"NEPHROTIC SYNDROME, TYPE 21",,,,,DOID:0112267,nephrotic syndrome type 21,C5231498,,618594;613397,MONDO:0032826,"nephrotic syndrome, type 21",
+BMGC_DS17963,BMG_DS068459,,"CORNEAL DYSTROPHY, MEESMANN, 1",,,,,DOID:0080670,Meesmann corneal dystrophy 1,C5231499,,122100;601687,MONDO:0020791,"corneal dystrophy, Meesmann, 1",
+BMGC_DS17964,BMG_DS068460,,CHROMOSOME 12q15 DELETION SYNDROME,,,,,,,C5231501,,618608,,,
+BMGC_DS17965,BMG_DS068468,,HEMOLYTIC ANEMIA DUE TO GLUTATHIONE REDUCTASE DEFICIENCY,,,,,DOID:0051009,congenital nonspherocytic hemolytic anemia 10,C5231513,,138300;618660,MONDO:0019531,hemolytic anemia due to glutathione reductase deficiency,
+BMGC_DS17966,BMG_DS068478,,"NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA, SEVERE",,,,,,,C5231533,,605712,,,
+BMGC_DS17967,BMG_DS068488,,"HYPOALPHALIPOPROTEINEMIA, PRIMARY, 1",,,,,DOID:0080957,primary hypoalphalipoproteinemia 1,C5231558,,604091,MONDO:0011393,"hypoalphalipoproteinemia, primary, 1",
+BMGC_DS17968,BMG_DS068490,,Secondary Vesicoureteral Reflux,Vesico-Ureteral Reflux,,,,,,C5232302,D014718,,,,
+BMGC_DS17969,BMG_DS068505,,Olfactory Impairment,Olfaction Disorders,,,,,,C5234846,D000857,,,,
+BMGC_DS17970,BMG_DS068506,,Antley-Bixler Syndrome,Antley-Bixler Syndrome Phenotype,,,,,,C5234850,D054882,,MONDO:0008803,Antley-Bixler syndrome,
+BMGC_DS17971,BMG_DS068507,,"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA",,,,,,,C5234852,,138250;219150,MONDO:0009053,ALDH18A1-related de Barsy syndrome,
+BMGC_DS17972,BMG_DS068509,,,,,,,,,C5234880,,,MONDO:0030831,gastrointestinal defect and immunodeficiency syndrome,
+BMGC_DS17973,BMG_DS068512,,Hemorrhagic Stroke,Hemorrhagic Stroke,,,,,,C5234922,D000083302,,,,
+BMGC_DS17974,BMG_DS068516,90635004;205474002;279082008,Acromesomelic dysplasia syndrome,,,,,,,C5235036,,,MONDO:0019696,acromesomelic dysplasia,Acromesomelic dysplasia syndrome | Acromesomelic dysplasia syndrome (disorder) | Acromesomelic dysplasia | Acromesomelic dwarfism | Acromesomelic dysplasia syndrome | Acromesomelic dysplasia (disorder) | Acromesomelic dysplasia syndrome | Acromesomelic dysplasia group | Acromesomelic dwarfism | Acromesomelic dysplasia | Acromesomelic dysplasia group (disorder)
+BMGC_DS17975,BMG_DS068518,,Cryptococcosis,Cryptococcosis,,,,,,C5235087,D003453,,,,
+BMGC_DS17976,BMG_DS068519,,,,,,,,,C5235139,,610357,MONDO:0012476,hereditary spastic paraplegia 30,
+BMGC_DS17977,BMG_DS068520,,"Neutropenia, Severe Congenital, Autosomal Recessive 3",,,,,,,C5235141,C537592,610738,MONDO:0012548,Kostmann syndrome,
+BMGC_DS17978,BMG_DS068525,789157007,Focal facial dermal dysplasia type I,,,,,,,C5235196,,136500,MONDO:0007627,focal facial dermal dysplasia type I,Focal facial dermal dysplasia type I | Brauer syndrome | Focal facial dermal dysplasia type I (disorder) | Focal facial dermal dysplasia 1 Brauer type | Bitemporal aplasia cutis congenita | FFDD type 1 - focal facial dermal dysplasia type 1
+BMGC_DS17979,BMG_DS068526,860813007,Hereditary sensory autonomic neuropathy type IA,,,,,,,C5235211,,162400,MONDO:0008086,"neuropathy, hereditary sensory and autonomic, type 1A",Hereditary sensory autonomic neuropathy type IA (disorder) | Hereditary sensory autonomic neuropathy type IA
+BMGC_DS17980,BMG_DS068535,,COFFIN-SIRIS SYNDROME 11,,,,,DOID:0112372,Coffin-Siris syndrome 11,C5241442,,601735;618779,MONDO:0032912,Coffin-Siris syndrome 11,
+BMGC_DS17981,BMG_DS068536,,"HYPOPARATHYROIDISM, FAMILIAL ISOLATED, 1",,,,,DOID:0111387,familial isolated hypoparathyroidism,C5241444,,146200;168450,MONDO:0007796,"hypoparathyroidism, familial isolated 1",
+BMGC_DS17982,BMG_DS068537,,,,,,,,,C5241445,,179300,MONDO:0100183,"radioulnar synostosis, nonsyndromic, susceptibility to",
+BMGC_DS17983,BMG_DS068539,,Emery-Dreifuss Muscular Dystrophy 1,X-Linked Emery-Dreifuss Muscular Dystrophy,,,,,,C5243475,D000083143,310300,MONDO:0100531,"Emery-Dreifuss muscular dystrophy 1, X-linked",
+BMGC_DS17984,BMG_DS068540,,Cardiometabolic Syndrome,Metabolic Syndrome,,,,,,C5243476,D024821,,,,
+BMGC_DS17985,BMG_DS068542,1208488006,Special AT-rich sequence-binding protein 2-associated syndrome,,,,,,,C5243581,,,,,SATB2-associated syndrome | Special AT-rich sequence-binding protein 2-associated syndrome | Special AT-rich sequence-binding protein 2-associated syndrome (disorder)
+BMGC_DS17986,BMG_DS068548,,,,,,,,,C5243927,,,MONDO:0100464,acid sphingomyelinase deficiency,
+BMGC_DS17987,BMG_DS068550,1222679006,"Autoimmune interstitial lung disease, arthritis syndrome",,,,,,,C5243948,,616414,MONDO:0014629,autoimmune interstitial lung disease-arthritis syndrome,"Autoimmune interstitial lung disease, arthritis syndrome (disorder) | COPA (coatomer protein complex subunit alpha) syndrome | Autoimmune interstitial lung disease, arthritis syndrome"
+BMGC_DS17988,BMG_DS068551,,,,,,,,,C5244016,,,MONDO:0000456,cerebral creatine deficiency syndrome,
+BMGC_DS17989,BMG_DS068552,882784691000119100,Pneumonia caused by SARS-CoV-2,,,,,,,C5244027,,,,,COVID-19 pneumonia | Pneumonia caused by SARS-CoV-2 | Pneumonia caused by 2019 novel coronavirus | Pneumonia caused by 2019-nCoV | Pneumonia caused by severe acute respiratory syndrome coronavirus 2 | Pneumonia caused by severe acute respiratory syndrome coronavirus 2 (disorder)
+BMGC_DS17990,BMG_DS068772,,Laminopathies,Laminopathies,,,,,,C5392094,D000083083,,MONDO:0021106,laminopathy,
+BMGC_DS17991,BMG_DS068773,,Cryptogenic Ischemic Stroke,Ischemic Stroke,,,,,,C5392097,D000083242,,,,
+BMGC_DS17992,BMG_DS068774,,Intracerebral Hemorrhagic Stroke,Hemorrhagic Stroke,,,,,,C5392098,D000083302,,,,
+BMGC_DS17993,BMG_DS068781,,"Respiratory Distress Syndrome, Pediatric",Respiratory Distress Syndrome,,,,,,C5392184,D012128,,,,
+BMGC_DS17994,BMG_DS068792,,Wake-up Stroke,Ischemic Stroke,,,,,,C5392832,D000083242,,,,
+BMGC_DS17995,BMG_DS068793,,Acute Ischemic Stroke,Ischemic Stroke,,,,,,C5392833,D000083242,,,,
+BMGC_DS17996,BMG_DS068795,,Subarachnoid Hemorrhagic Stroke,Hemorrhagic Stroke,,,,,,C5392835,D000083302,,,,
+BMGC_DS17997,BMG_DS068805,,Smell Dysfunction,Olfaction Disorders,,,,,,C5392883,D000857,,,,
+BMGC_DS17998,BMG_DS068814,,Taste Dysfunction,Taste Disorders,,,,,,C5392959,D013651,,,,
+BMGC_DS17999,BMG_DS068815,,Pityriasis Folliculitis,Tinea Versicolor,,,,,,C5392960,D014010,,,,
+BMGC_DS18000,BMG_DS068819,,SILVER-RUSSELL SYNDROME 1,,,,,,,C5393125,,180860,MONDO:0020796,Silver-Russell syndrome 1,
+BMGC_DS18001,BMG_DS068822,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE",,,,,,,C5393299,,300160;300958,MONDO:0010497,"intellectual disability, X-linked 102",
+BMGC_DS18002,BMG_DS068823,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE",,,,,,,C5393302,,301039;300766,MONDO:0026733,"intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type",
+BMGC_DS18003,BMG_DS068824,,"WIEACKER-WOLFF SYNDROME, FEMALE-RESTRICTED",,,,,DOID:0061015,female-restricted Wieacker-Wolff syndrome,C5393303,,301041;300897,MONDO:0026762,"Wieacker-Wolff syndrome, female-restricted",
+BMGC_DS18004,BMG_DS068825,,"HOLOPROSENCEPHALY 13, X-LINKED",,,,,DOID:0060954,"Holoprosencephaly 13, X-linked",C5393308,,300826;301043,MONDO:0026763,"holoprosencephaly 13, X-linked",
+BMGC_DS18005,BMG_DS068826,,,,,,,,,C5393309,,,MONDO:0017219,microform holoprosencephaly,
+BMGC_DS18006,BMG_DS068827,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 85 WITH OR WITHOUT MIDLINE BRAIN DEFECTS,,,,,DOID:0070380,developmental and epileptic encephalopathy 85,C5393312,,300040;301044,MONDO:0026771,"developmental and epileptic encephalopathy, 85, with or without midline brain defects",
+BMGC_DS18007,BMG_DS068828,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIr",,,,,,,C5393313,,301045;300556,MONDO:0026765,"congenital disorder of glycosylation, type IIr",
+BMGC_DS18008,BMG_DS068829,,"DIABETES MELLITUS, PERMANENT NEONATAL, 1",,,,,DOID:0060639,permanent neonatal diabetes mellitus,C5393570,,138079;606176,MONDO:0100165,permanent neonatal diabetes mellitus 1,
+BMGC_DS18009,BMG_DS068831,,,,,,,,,C5393830,,614255,MONDO:0013656,"intellectual disability, autosomal dominant 9",
+BMGC_DS18010,BMG_DS068832,,HAO-FOUNTAIN SYNDROME,,,,,,,C5393908,,616863;602519,MONDO:0014805,Hao-Fountain syndrome,
+BMGC_DS18011,BMG_DS068833,,"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, SPASTICITY, AND BRAIN ATROPHY",,,,,,,C5394027,,618741;610971,MONDO:0032894,"neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy",
+BMGC_DS18012,BMG_DS068834,,"SPASTIC PARAPLEGIA 81, AUTOSOMAL RECESSIVE",,,,,DOID:0112349,hereditary spastic paraplegia 81,C5394033,,618768;607915,MONDO:0032905,"spastic paraplegia 81, autosomal recessive",
+BMGC_DS18013,BMG_DS068835,,"SPASTIC PARAPLEGIA 82, AUTOSOMAL RECESSIVE",,,,,DOID:0112343,hereditary spastic paraplegia 82,C5394037,,618770;602679,MONDO:0032906,"spastic paraplegia 82, autosomal recessive",
+BMGC_DS18014,BMG_DS068836,,CEBALID SYNDROME,,,,,,,C5394044,,156100;618774,MONDO:0032908,CEBALID syndrome,
+BMGC_DS18015,BMG_DS068837,,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 10",,,,,,,C5394051,,191327;618775,MONDO:0032909,"mitochondrial complex 3 deficiency, nuclear type 10",
+BMGC_DS18016,BMG_DS068838,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 34",,,,,DOID:0112091,nuclear type mitochondrial complex I deficiency 34,C5394053,,618776;618461,MONDO:0032910,"mitochondrial complex 1 deficiency, nuclear type 34",
+BMGC_DS18017,BMG_DS068839,,"DEAFNESS, AUTOSOMAL DOMINANT 75",,,,,DOID:0112166,autosomal dominant nonsyndromic deafness 75,C5394059,,618778;603015,MONDO:0032911,"hearing loss, autosomal dominant 75",
+BMGC_DS18018,BMG_DS068840,,,,,,,,,C5394062,,618780,MONDO:0032913,"congenital heart defects, multiple types, 7",
+BMGC_DS18019,BMG_DS068841,,"CILIARY DYSKINESIA, PRIMARY, 44",,,,,DOID:0111851,primary ciliary dyskinesia 44,C5394063,,618726;618781,MONDO:0032914,"ciliary dyskinesia, primary, 44",
+BMGC_DS18020,BMG_DS068842,,LONG QT SYNDROME 16,,,,,DOID:0070533,long QT syndrome 16,C5394068,,114183;618782,MONDO:0032915,long QT syndrome 16,
+BMGC_DS18021,BMG_DS068843,,"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 6",,,,,,,C5394069,,114183,MONDO:0800374,"ventricular tachycardia, catecholaminergic polymorphic 6",
+BMGC_DS18022,BMG_DS068844,,IMAGAWA-MATSUMOTO SYNDROME,,,,,,,C5394073,,606245;618786,MONDO:0032916,Imagawa-Matsumoto syndrome,
+BMGC_DS18023,BMG_DS068845,,"DEAFNESS, AUTOSOMAL DOMINANT 76",,,,,DOID:0112167,autosomal dominant nonsyndromic deafness 76,C5394080,,618787;602734,MONDO:0032917,"hearing loss, autosomal dominant 76",
+BMGC_DS18024,BMG_DS068846,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 84,,,,,DOID:0112219,developmental and epileptic encephalopathy 84,C5394081,,618792;603370,MONDO:0032918,"developmental and epileptic encephalopathy, 84",
+BMGC_DS18025,BMG_DS068847,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62",,,,,,,C5394083,,602887;618793,MONDO:0032919,intellectual developmental disorder 62,
+BMGC_DS18026,BMG_DS068848,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEONATAL RESPIRATORY INSUFFICIENCY, AND THERMODYSREGULATION",,,,,,,C5394091,,608884;618797,MONDO:0032921,"neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation",
+BMGC_DS18027,BMG_DS068849,,BECK-FAHRNER SYNDROME,,,,,,,C5394097,,618798,MONDO:0032922,Beck-Fahrner syndrome,
+BMGC_DS18028,BMG_DS068850,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 28",,,,,DOID:0070409,autosomal recessive spinocerebellar ataxia 28,C5394101,,618800;618802,MONDO:0032923,"spinocerebellar ataxia, autosomal recessive 28",
+BMGC_DS18029,BMG_DS068851,,"CILIARY DYSKINESIA, PRIMARY, 45",,,,,DOID:0111857,primary ciliary dyskinesia 45,C5394104,,618801;610732,MONDO:0032924,"ciliary dyskinesia, primary, 45",
+BMGC_DS18030,BMG_DS068852,,"RESPIRATORY PAPILLOMATOSIS, JUVENILE RECURRENT, CONGENITAL",,,,,,,C5394112,,618803;606636,MONDO:0032925,"respiratory papillomatosis, juvenile recurrent, congenital",
+BMGC_DS18031,BMG_DS068853,,SANDESTIG-STEFANOVA SYNDROME,,,,,DOID:0081272,Sandestig-Stefanova syndrome,C5394118,,618804;615587,MONDO:0032926,sandestig-stefanova syndrome,
+BMGC_DS18032,BMG_DS068854,,TRIOKINASE AND FMN CYCLASE DEFICIENCY SYNDROME,,,,,,,C5394125,,615844;618805,MONDO:0032927,triokinase and FMN cyclase deficiency syndrome,
+BMGC_DS18033,BMG_DS068855,,"T-CELL LYMPHOPENIA, INFANTILE, WITH OR WITHOUT NAIL DYSTROPHY, AUTOSOMAL DOMINANT",,,,,,,C5394133,,600838;618806,MONDO:0032928,"T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant",
+BMGC_DS18034,BMG_DS068856,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH POOR GROWTH AND WITH OR WITHOUT SEIZURES OR ATAXIA,,,,,,,C5394135,,618808,MONDO:0032930,intellectual developmental disorder with poor growth and with or without seizures or ataxia,
+BMGC_DS18035,BMG_DS068857,,"PONTOCEREBELLAR HYPOPLASIA, HYPOTONIA, AND RESPIRATORY INSUFFICIENCY SYNDROME, NEONATAL LETHAL",,,,,DOID:0081396,"neonatal lethal pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome",C5394137,,618810;612316,MONDO:0032931,"pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal",
+BMGC_DS18036,BMG_DS068858,,MITOCHONDRIAL DNA DEPLETION SYNDROME 18,,,,,DOID:0070449,mitochondrial DNA depletion syndrome 18,C5394140,,607571;618811,MONDO:0032932,mitochondrial DNA depletion syndrome 18,
+BMGC_DS18037,BMG_DS068859,,"CHROMOSOME 1p36.33 DUPLICATION SYNDROME, ATAD3 GENE CLUSTER, AUTOSOMAL DOMINANT",,,,,DOID:0070470,chromosome 1p36.33 duplication syndrome,C5394150,,618815,MONDO:0032933,"chromosome 1p36.33 duplication syndrome, atad3 gene cluster, autosomal dominant",
+BMGC_DS18038,BMG_DS068860,,GENITOURINARY AND/OR BRAIN MALFORMATION SYNDROME,,,,,,,C5394158,,618820;602021,MONDO:0032934,genitourinary and/or brain malformation syndrome,
+BMGC_DS18039,BMG_DS068861,,RHIZOMELIC LIMB SHORTENING WITH DYSMORPHIC FEATURES,,,,,,,C5394173,,618821;614150,MONDO:0032935,rhizomelic limb shortening with dysmorphic features,
+BMGC_DS18040,BMG_DS068862,,CONGENITAL MYOPATHY 9A,,,,,DOID:0081343,congenital myopathy 9A,C5394189,,618822,MONDO:0032936,"myopathy, congenital, with respiratory insufficiency and bone fractures",
+BMGC_DS18041,BMG_DS068863,,"CONGENITAL MYOPATHY 9B, PROXIMAL, WITH MINICORE LESIONS",,,,,DOID:0081344,congenital myopathy 9B,C5394193,,600819;618823,MONDO:0032937,"myopathy, congenital proximal, with minicore lesions",
+BMGC_DS18042,BMG_DS068864,,"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 8, AUTOSOMAL RECESSIVE",,,,,,,C5394199,,618824;606870,MONDO:0032938,"basal ganglia calcification, idiopathic, 8, autosomal recessive",
+BMGC_DS18043,BMG_DS068865,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 63, WITH MACROCEPHALY",,,,,,,C5394205,,601893;618825,MONDO:0032939,"intellectual developmental disorder, autosomal dominant 63, with macrocephaly",
+BMGC_DS18044,BMG_DS068866,,RETINITIS PIGMENTOSA 88,,,,,DOID:0112145,retinitis pigmentosa 88,C5394208,,618826;608581,MONDO:0032940,retinitis pigmentosa 88,
+BMGC_DS18045,BMG_DS068867,,"MYOPIA 27, AUTOSOMAL DOMINANT",,,,,,,C5394215,,618827,MONDO:0032941,myopia 27,
+BMGC_DS18046,BMG_DS068868,,"NABAIS SA-DE VRIES SYNDROME, TYPE 1",,,,,,,C5394218,,602650;618828,MONDO:0032942,neurodevelopmental disorder with microcephaly and dysmorphic facies,
+BMGC_DS18047,BMG_DS068869,,"NABAIS SA-DE VRIES SYNDROME, TYPE 2",,,,,,,C5394221,,602650;618829,MONDO:0032943,neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies,
+BMGC_DS18048,BMG_DS068870,,,,,,,,,C5394226,,618830,MONDO:0030004,"autism, susceptibility to, 20",
+BMGC_DS18049,BMG_DS068871,1197430005,QRSL1-related combined oxidative phosphorylation defect,,,,,,,C5394232,,618835,MONDO:0030006,combined oxidative phosphorylation deficiency 40,QRSL1-related combined oxidative phosphorylation defect | Glutaminyl-transfer ribonucleic acid amidotransferase subunit-related combined oxidative phosphorylation defect (disorder) | Glutaminyl-transfer ribonucleic acid amidotransferase subunit-related combined oxidative phosphorylation defect
+BMGC_DS18050,BMG_DS068872,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 41,,,,,DOID:0112119,combined oxidative phosphorylation deficiency 41,C5394236,,618838;603645,MONDO:0030007,combined oxidative phosphorylation deficiency 41,
+BMGC_DS18051,BMG_DS068873,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 42,,,,,DOID:0112118,combined oxidative phosphorylation deficiency 42,C5394237,,618839;617210,MONDO:0030008,combined oxidative phosphorylation deficiency 42,
+BMGC_DS18052,BMG_DS068874,,ALOPECIA-INTELLECTUAL DISABILITY SYNDROME 4,,,,,DOID:0080950,alopecia-mental retardation syndrome 4,C5394241,,600909;618840,MONDO:0030009,alopecia-intellectual disability syndrome 4,
+BMGC_DS18053,BMG_DS068875,,HYPOGONADOTROPIC HYPOGONADISM 25 WITH ANOSMIA,,,,,,,C5394246,,616506;618841,MONDO:0030010,hypogonadotropic hypogonadism 25 with anosmia,
+BMGC_DS18054,BMG_DS068876,,"VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 3",,,,,,,C5394250,,608285;618845,MONDO:0030077,"vertebral, cardiac, renal, and limb defects syndrome 3",
+BMGC_DS18055,BMG_DS068877,,DIETS-JONGMANS SYNDROME,,,,,,,C5394263,,618846;609373,MONDO:0030012,Diets-Jongmans syndrome,
+BMGC_DS18056,BMG_DS068878,,IMMUNODEFICIENCY 66,,,,,DOID:0111998,immunodeficiency 66,C5394265,,606078;618847,MONDO:0030013,immunodeficiency 66,
+BMGC_DS18057,BMG_DS068879,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 26",,,,,,,C5394268,,605824;618848,MONDO:0030014,"muscular dystrophy, limb-girdle, autosomal recessive 26",
+BMGC_DS18058,BMG_DS068880,,BONE MARROW FAILURE SYNDROME 6,,,,,,,C5394274,,602704;618849,MONDO:0030015,bone marrow failure syndrome 6,
+BMGC_DS18059,BMG_DS068881,,HYPERVALINEMIA AND HYPERLEUCINE-ISOLEUCINEMIA,,,,,DOID:0060950,hypervalinemia and hyperleucine-isoleucinemia,C5394277,,113530;618850,MONDO:0100058,hypervalinemia and hyperleucine-isoleucinemia,
+BMGC_DS18060,BMG_DS068882,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 43,,,,,DOID:0112116,combined oxidative phosphorylation deficiency 43,C5394284,,607251;618851,MONDO:0030017,combined oxidative phosphorylation deficiency 43,
+BMGC_DS18061,BMG_DS068883,,,,,,,,,C5394286,,618852,MONDO:0030018,autoinflammation with episodic fever and lymphadenopathy,
+BMGC_DS18062,BMG_DS068884,,ANAUXETIC DYSPLASIA 3,,,,,DOID:0080963,anauxetic dysplasia 3,C5394289,,618853;617089,MONDO:0030019,anauxetic dysplasia 3,
+BMGC_DS18063,BMG_DS068885,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 44,,,,,DOID:0070424,combined oxidative phosphorylation deficiency 44,C5394293,,618855;612322,MONDO:0030020,combined oxidative phosphorylation deficiency 44,
+BMGC_DS18064,BMG_DS068886,,"DIABETES MELLITUS, PERMANENT NEONATAL, 2",,,,,,,C5394296,,600937;618856,MONDO:0030087,"diabetes mellitus, permanent neonatal 2",
+BMGC_DS18065,BMG_DS068887,,"DIABETES MELLITUS, PERMANENT NEONATAL, 3",,,,,,,C5394303,,600509;618857,MONDO:0030088,"diabetes mellitus, permanent neonatal 3",
+BMGC_DS18066,BMG_DS068888,,"DEVELOPMENTAL DELAY, EPILEPSY, AND NEONATAL DIABETES 2",,,,,,,C5394304,,618857,MONDO:0800376,"developmental delay, epilepsy, and neonatal diabetes 2",
+BMGC_DS18067,BMG_DS068889,,"DIABETES MELLITUS, PERMANENT NEONATAL, 4",,,,,,,C5394307,,176730;618858,MONDO:0030089,"diabetes mellitus, permanent neonatal 4",
+BMGC_DS18068,BMG_DS068890,,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISTIC FEATURES AND/OR STRUCTURAL BRAIN ABNORMALITIES,,,,,,,C5394311,,618859,MONDO:0030024,neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities,
+BMGC_DS18069,BMG_DS068891,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, MICROCEPHALY, AND SEIZURES",,,,,,,C5394312,,618862;601218,MONDO:0030025,"neurodevelopmental disorder with hypotonia, microcephaly, and seizures",
+BMGC_DS18070,BMG_DS068892,,RETINAL DYSTROPHY WITH LEUKODYSTROPHY,,,,,DOID:0080946,retinal dystrophy with leukodystrophy,C5394315,,616618;618863,MONDO:0030026,retinal dystrophy with leukodystrophy,
+BMGC_DS18071,BMG_DS068893,,"TREMOR, HEREDITARY ESSENTIAL, 6",,,,,DOID:0081295,essential tremor 6,C5394329,,618866,MONDO:0030027,"tremor, hereditary essential, 6",
+BMGC_DS18072,BMG_DS068894,,"NEURODEGENERATION, CHILDHOOD-ONSET, WITH ATAXIA, TREMOR, OPTIC ATROPHY, AND COGNITIVE DECLINE",,,,,,,C5394335,,618868;606105,MONDO:0030028,"neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline",
+BMGC_DS18073,BMG_DS068895,,"SKELETAL DYSPLASIA, MILD, WITH JOINT LAXITY AND ADVANCED BONE AGE",,,,,,,C5394341,,618870;616615,MONDO:0030029,"skeletal dysplasia, mild, with joint laxity and advanced bone age",
+BMGC_DS18074,BMG_DS068896,,NIZON-ISIDOR SYNDROME,,,,,,,C5394350,,618872;611318,MONDO:0030030,Nizon-Isidor syndrome,
+BMGC_DS18075,BMG_DS068897,,LISSENCEPHALY 10,,,,,DOID:0112229,lissencephaly 10,C5394354,,618873;618865,MONDO:0030031,lissencephaly 10,
+BMGC_DS18076,BMG_DS068898,,"SEIZURES, EARLY-ONSET, WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS",,,,,,,C5394359,,615322;618875,MONDO:0030033,"seizures, early-onset, with neurodegeneration and brain calcifications",
+BMGC_DS18077,BMG_DS068899,,"EPILEPSY, PROGRESSIVE MYOCLONIC, 11",,,,,,,C5394362,,608873;618876,MONDO:0030034,"epilepsy, progressive myoclonic, 11",
+BMGC_DS18078,BMG_DS068900,,"LEUKOENCEPHALOPATHY, DEVELOPMENTAL DELAY, AND EPISODIC NEUROLOGIC REGRESSION SYNDROME",,,,,,,C5394367,,176871;618877,MONDO:0030035,"leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome",
+BMGC_DS18079,BMG_DS068901,,"LEUKOENCEPHALOPATHY, MOTOR DELAY, SPASTICITY, AND DYSARTHRIA SYNDROME",,,,,,,C5394371,,613635;618878,MONDO:0030036,"leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome",
+BMGC_DS18080,BMG_DS068902,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CEREBELLAR ATROPHY, WITH OR WITHOUT SEIZURES",,,,,,,C5394372,,605087;618879,MONDO:0030037,"neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures",
+BMGC_DS18081,BMG_DS068903,,"GLAUCOMA, PRIMARY CLOSED-ANGLE",,,,,,,C5394374,,618880,MONDO:0030038,"glaucoma, primary closed-angle",
+BMGC_DS18082,BMG_DS068904,1187616008,Deficiency of galactose mutarotase,,,,,,,C5394377,,618881,MONDO:0030105,galactosemia 4,Galactosemia type 4 | Galactosaemia type 4 | GALM (galactose mutarotase) deficiency | Deficiency of galactose mutarotase | Deficiency of galactose mutarotase (disorder)
+BMGC_DS18083,BMG_DS068905,,"HYPOPARATHYROIDISM, FAMILIAL ISOLATED, 2",,,,,,,C5394383,,618883;603716,MONDO:0020798,"hypoparathyroidism, familial isolated, 2",
+BMGC_DS18084,BMG_DS068906,,,,,,,,,C5394384,,618884,MONDO:0030042,"proteinuria, chronic benign",
+BMGC_DS18085,BMG_DS068907,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIt",,,,,,,C5394387,,602274;618885,MONDO:0030043,"congenital disorder of glycosylation, type iit",
+BMGC_DS18086,BMG_DS068908,,PSEUDO-TORCH SYNDROME 3,,,,,,,C5394391,,600556;618886,MONDO:0030044,pseudo-TORCH syndrome 3,
+BMGC_DS18087,BMG_DS068910,1284851009,"Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome",,,,,,,C5394404,,618889,MONDO:0030045,Liberfarb syndrome,"Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome | Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome (disorder) | Liberfarb syndrome"
+BMGC_DS18088,BMG_DS068911,,NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY,,,,,,,C5394423,,618890,MONDO:0030046,neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity,
+BMGC_DS18089,BMG_DS068912,,"MICROCEPHALY, DEVELOPMENTAL DELAY, AND BRITTLE HAIR SYNDROME",,,,,,,C5394425,,123859;618891,MONDO:0030047,"microcephaly, developmental delay, and brittle hair syndrome",
+BMGC_DS18090,BMG_DS068913,,"46,XX SEX REVERSAL 5",,,,,DOID:0080943,"46,XX sex reversal 5",C5394441,,618901;107773,MONDO:0030049,"46,xx sex reversal 5",
+BMGC_DS18091,BMG_DS068914,,SILVER-RUSSELL SYNDROME 2,,,,,,,C5394446,,618905,MONDO:0030116,silver-russell syndrome 2,
+BMGC_DS18092,BMG_DS068915,,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES",,,,,DOID:0081430,"intellectual developmental disorder with autistic features and language delay, with or without seizures",C5394447,,618906,MONDO:0030051,"intellectual developmental disorder with autistic features and language delay, with or without seizures",
+BMGC_DS18093,BMG_DS068916,,SILVER-RUSSELL SYNDROME 4,,,,,,,C5394450,,618907;603026,MONDO:0030118,silver-russell syndrome 4,
+BMGC_DS18094,BMG_DS068917,,SILVER-RUSSELL SYNDROME 5,,,,,,,C5394456,,600698;618908,MONDO:0020795,Silver-Russell syndrome 5,
+BMGC_DS18095,BMG_DS068918,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 86,,,,,DOID:0112220,developmental and epileptic encephalopathy 86,C5394462,,618910;618904,MONDO:0030054,"developmental and epileptic encephalopathy, 86",
+BMGC_DS18096,BMG_DS068919,,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL RECESSIVE 8",,,,,DOID:0081427,autosomal recessive distal hereditary motor neuronopathy 8,C5394466,,182500;618912,MONDO:0030055,"neuronopathy, distal hereditary motor, autosomal recessive 8",
+BMGC_DS18097,BMG_DS068920,,FANCONI RENOTUBULAR SYNDROME 5,,,,,DOID:0080761,Fanconi renotubular syndrome 5,C5394473,,612392;618913,MONDO:0030056,Fanconi renotubular syndrome 5,
+BMGC_DS18098,BMG_DS068921,,"NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME",,,,,,,C5394477,,618914;605651,MONDO:0030057,"neurodevelopmental, jaw, eye, and digital syndrome",
+BMGC_DS18099,BMG_DS068922,,"DEAFNESS, AUTOSOMAL DOMINANT 77",,,,,DOID:0112168,autosomal dominant nonsyndromic deafness 77,C5394499,,618915;158343,MONDO:0030058,"hearing loss, autosomal dominant 77",
+BMGC_DS18100,BMG_DS068923,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 87,,,,,DOID:0112221,developmental and epileptic encephalopathy 87,C5394501,,614720;618916,MONDO:0030059,"developmental and epileptic encephalopathy, 87",
+BMGC_DS18101,BMG_DS068924,,NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND BEHAVIORAL ABNORMALITIES,,,,,,,C5394502,,138247;618917,MONDO:0030060,neurodevelopmental disorder with language impairment and behavioral abnormalities,
+BMGC_DS18102,BMG_DS068925,,PERIVENTRICULAR NODULAR HETEROTOPIA 9,,,,,,,C5394503,,157129;618918,MONDO:0030061,periventricular nodular heterotopia 9,
+BMGC_DS18103,BMG_DS068926,,"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 14",,,,,DOID:0080959,arrhythmogenic right ventricular dysplasia 14,C5394505,,618920;114020,MONDO:0030062,"arrhythmogenic right ventricular dysplasia, familial, 14",
+BMGC_DS18104,BMG_DS068927,,"NEURODEVELOPMENTAL DISORDER WITH SEIZURES, HYPOTONIA, AND BRAIN IMAGING ABNORMALITIES",,,,,,,C5394517,,618922;604101,MONDO:0030063,"neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities",
+BMGC_DS18105,BMG_DS068928,,"EPISODIC ATAXIA, TYPE 9",,,,,DOID:0060965,episodic ataxia type 9,C5394520,,618924;182390,MONDO:0030064,"episodic ataxia, type 9",
+BMGC_DS18106,BMG_DS068929,,"AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME",,,,,DOID:0080948,"agenesis of corpus callosum, cardiac, ocular, and genital syndrome",C5394523,,618929;114020,MONDO:0030065,"agenesis of corpus callosum, cardiac, ocular, and genital syndrome",
+BMGC_DS18107,BMG_DS068930,,"GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 5",,,,,DOID:0070368,autosomal recessive chronic granulomatous disease 5,C5394542,,618334;618935,MONDO:0030066,"granulomatous disease, chronic, autosomal recessive, 5",
+BMGC_DS18108,BMG_DS068931,,TREACHER COLLINS SYNDROME 4,,,,,DOID:0080792,Treacher Collins syndrome 4,C5394546,,618939;602000,MONDO:0030067,Treacher Collins syndrome 4,
+BMGC_DS18109,BMG_DS068932,,,,,,,,,C5394548,,618940,MONDO:0030134,oculopharyngodistal myopathy 2,
+BMGC_DS18110,BMG_DS068933,,"HYPER-IgE SYNDROME 5, AUTOSOMAL RECESSIVE, WITH RECURRENT INFECTIONS",,,,,,,C5394550,,618944;147880,MONDO:0030069,"hyper-IgE recurrent infection syndrome 5, autosomal recessive",
+BMGC_DS18111,BMG_DS068934,,"HETEROTAXY, VISCERAL, 9, AUTOSOMAL, WITH MALE INFERTILITY",,,,,,,C5394551,,618948;610766,MONDO:0030070,"heterotaxy, visceral, 9, autosomal, with male infertility",
+BMGC_DS18112,BMG_DS068935,,RETINITIS PIGMENTOSA 89,,,,,DOID:0112146,retinitis pigmentosa 89,C5394552,,618955;603754,MONDO:0030071,retinitis pigmentosa 89,
+BMGC_DS18113,BMG_DS068936,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 88,,,,,DOID:0112222,developmental and epileptic encephalopathy 88,C5394553,,154200;618959,MONDO:0030072,"developmental and epileptic encephalopathy, 88",
+BMGC_DS18114,BMG_DS068937,,,,,,,DOID:0070516,Mitchell syndrome,C5394554,,618960,MONDO:0030073,Mitchell syndrome,
+BMGC_DS18115,BMG_DS068938,1269226006,"Spondylometaphyseal dysplasia, corneal dystrophy syndrome",,,,,,,C5394555,,618961,MONDO:0030074,spondylometaphyseal dysplasia with corneal dystrophy,"Spondylometaphyseal dysplasia, corneal dystrophy syndrome | Spondylometaphyseal dysplasia, corneal dystrophy syndrome (disorder)"
+BMGC_DS18116,BMG_DS068968,,"CHROMOSOME 1p36.33 DELETION SYNDROME, ATAD3 GENE CLUSTER, AUTOSOMAL RECESSIVE",,,,,DOID:0081396,"neonatal lethal pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome",C5394596,,618810,,,
+BMGC_DS18117,BMG_DS068969,,"DEVELOPMENTAL DELAY, EPILEPSY, AND NEONATAL DIABETES 1",,,,,,,C5394597,,618856,MONDO:0800375,"developmental delay, epilepsy, and neonatal diabetes 1",
+BMGC_DS18118,BMG_DS068972,829973009,Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis,,,,,,,C5394674,,,MONDO:0017992,autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis,Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis | Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis (disorder)
+BMGC_DS18119,BMG_DS069019,,,,,,,,,C5395080,,,MONDO:0020316,acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22),
+BMGC_DS18120,BMG_DS069445,870286003,Pelizaeus Merzbacher like disease due to AIMP1 mutation,,,,,,,C5396702,,,,,Pelizaeus Merzbacher like disease due to AIMP1 mutation (disorder) | Pelizaeus Merzbacher like disease due to AIMP1 mutation
+BMGC_DS18121,BMG_DS069651,41283003,Cerebro-oculo-facio-skeletal syndrome,,,,,,,C5399761,,,MONDO:0008926,COFS syndrome,Cerebro-oculo-facio-skeletal syndrome | COFS syndrome | Cerebro-oculo-facio-skeletal syndrome (disorder) | CAMAK - Cerebro-oculo-facio-skeletal syndrome | CAMFAK - Cerebro-oculo-facio-skeletal syndrome | COFS - Cerebro-oculo-facio-skeletal syndrome | Pena-Shokeir syndrome type 2
+BMGC_DS18122,BMG_DS069652,,,,,,,,,C5399762,,305450,MONDO:0010590,FG syndrome 1,
+BMGC_DS18123,BMG_DS069653,,mismatch repair cancer syndrome 1,,,,,,,C5399763,C536928,276300,MONDO:0010159,mismatch repair cancer syndrome 1,
+BMGC_DS18124,BMG_DS069656,1003431005,Mandibuloacral dysplasia with type A lipodystrophy,,,,,,,C5399785,C535705,248370,MONDO:0009557,mandibuloacral dysplasia with type A lipodystrophy,Mandibuloacral dysostosis co-occurrent with type A lipodystrophy (disorder) | Mandibuloacral dysostosis co-occurrent with type A lipodystrophy | Mandibuloacral dysplasia with type A lipodystrophy
+BMGC_DS18125,BMG_DS069659,,"LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1",,,,,,,C5399825,,308240;300490,MONDO:0024551,X-linked lymphoproliferative disease due to SH2D1A deficiency,
+BMGC_DS18126,BMG_DS069660,,"Familial Mediterranean Fever, Autosomal Recessive",Familial Mediterranean Fever,,,,,,C5399837,D010505,,,,
+BMGC_DS18127,BMG_DS069661,,,,,,,,,C5399870,,272150,MONDO:0010087,Sugarman brachydactyly,
+BMGC_DS18128,BMG_DS069662,784352007,X-linked scapuloperoneal muscular dystrophy,,,,,,,C5399872,,,,,X-linked scapuloperoneal muscular dystrophy (disorder) | X-linked scapuloperoneal muscular dystrophy | X-linked scapuloperoneal syndrome
+BMGC_DS18129,BMG_DS069664,,Brachyolmia Type 2,,,,,,,C5399913,C563218,613678,MONDO:0013360,"brachyolmia, Maroteaux type",
+BMGC_DS18130,BMG_DS069665,,,,,,,DOID:7221,gallbladder papillary carcinoma,C5399921,,,,,
+BMGC_DS18131,BMG_DS069666,,FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1,,,,,DOID:0111192,facioscapulohumeral muscular dystrophy 1,C5399970,,158900,MONDO:0008030,facioscapulohumeral muscular dystrophy 1,
+BMGC_DS18132,BMG_DS069667,,"IFAP SYNDROME 1, WITH OR WITHOUT BRESHECK SYNDROME",,,,,,,C5399971,,308205,MONDO:0100213,"IFAP syndrome 1, with or without BRESHECK syndrome",
+BMGC_DS18133,BMG_DS069668,,Periventricular heterotopia,,,,,,,C5399973,,MTHU022782,,,
+BMGC_DS18134,BMG_DS069669,,"ROBINOW SYNDROME, AUTOSOMAL RECESSIVE 1",,,,,DOID:0060764,autosomal recessive Robinow syndrome,C5399974,,268310;602337,MONDO:0009999,autosomal recessive Robinow syndrome,
+BMGC_DS18135,BMG_DS069670,,"MYOPATHY, DISTAL, WITH RIMMED VACUOLES",,,,,DOID:0081363,distal myopathy with rimmed vacuoles,C5399975,,601530;617158,MONDO:0014945,"myopathy, distal, with rimmed vacuoles",
+BMGC_DS18136,BMG_DS069671,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 2",,,,,DOID:0080357,mitochondrial complex IV deficiency nuclear type 2,C5399977,,604272;604377,MONDO:0011451,"cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1",
+BMGC_DS18137,BMG_DS069672,,"RENAL TUBULAR ACIDOSIS, DISTAL, 3, WITH OR WITHOUT SENSORINEURAL HEARING LOSS",,,,,,,C5399980,,605239;602722,MONDO:0011268,"renal tubular acidosis, distal, 3, with or without sensorineural hearing loss",
+BMGC_DS18138,BMG_DS069680,,,,,,,,,C5400698,,,MONDO:0001437,pulmonary alveolar proteinosis,
+BMGC_DS18139,BMG_DS069683,880093002,17q11 deletion syndrome,,,,,,,C5401456,,613675,MONDO:0013357,"chromosome 17q11.2 deletion syndrome, 1.4Mb",17q11 deletion syndrome (disorder) | 17q11 deletion syndrome | Neurofibromatosis type 1 microdeletion syndrome | Monosomy 17q11 | Chromosome 17q11.2 deletion syndrome
+BMGC_DS18140,BMG_DS069688,,,,,,,DOID:8216,parapharyngeal meningioma,C5421232,,,,,
+BMGC_DS18141,BMG_DS069704,,OPTIC ATROPHY 13 WITH RETINAL AND FOVEAL ABNORMALITIES,,,,,,,C5435585,,165510;600439,MONDO:0008135,optic atrophy 13 with retinal and foveal abnormalities,
+BMGC_DS18142,BMG_DS069705,,"MICROCORNEA, ROD-CONE DYSTROPHY, CATARACT, AND POSTERIOR STAPHYLOMA 2",,,,,,,C5435648,,193220;607854,MONDO:0800296,"microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 2",
+BMGC_DS18143,BMG_DS069706,,"ARTHROGRYPOSIS MULTIPLEX CONGENITA 2, NEUROGENIC TYPE",,,,,,,C5435650,,208100;617946,MONDO:0008823,"arthrogryposis multiplex congenita 2, neurogenic type",
+BMGC_DS18144,BMG_DS069707,,COACH SYNDROME 1,,,,,,,C5435651,,609884;216360,MONDO:0800103,COACH syndrome 1,
+BMGC_DS18145,BMG_DS069708,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 1",,,,,DOID:0070491,mitochondrial complex IV deficiency nuclear type 1,C5435656,,220110;185620,MONDO:0700250,"mitochondrial complex IV deficiency, nuclear type 1",
+BMGC_DS18146,BMG_DS069709,,TYPE 1 DIABETES MELLITUS 1,,,,,,,C5435660,,222100,MONDO:0009100,type 1 diabetes mellitus 1,
+BMGC_DS18147,BMG_DS069710,,PALLISTER-HALL-LIKE SYNDROME,,,,,,,C5435677,,241800;601500,,,
+BMGC_DS18148,BMG_DS069711,,"GROWTH HORMONE INSENSITIVITY SYNDROME WITH IMMUNE DYSREGULATION 1, AUTOSOMAL RECESSIVE",,,,,DOID:0080836,growth hormone insensitivity syndrome with immune dysregulation 1,C5435698,,604260;245590,MONDO:0100211,"growth hormone insensitivity with immune dysregulation 1, autosomal recessive",
+BMGC_DS18149,BMG_DS069712,,"IMMUNODEFICIENCY 74, COVID19-RELATED, X-LINKED",,,,,DOID:0112063,X-Linked immunodeficiency 74,C5435745,,301051,MONDO:0026767,"immunodeficiency 74, COVID-19-related, X-linked",
+BMGC_DS18150,BMG_DS069713,1290093003,VEXAS syndrome,,,,,,,C5435753,C000721467,301054,MONDO:0026777,VEXAS syndrome,"VEXAS syndrome | Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome (disorder) | Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome"
+BMGC_DS18151,BMG_DS069714,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, MITOCHONDRIAL FORM, 1",,,,,,,C5435765,,500013;590105,MONDO:0025622,"Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1",
+BMGC_DS18152,BMG_DS069716,,"46,XY GONADAL DYSGENESIS WITH MINIFASCICULAR NEUROPATHY",,,,,,,C5436061,,605423;607080,MONDO:0011766,"46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome",
+BMGC_DS18153,BMG_DS069718,,"RENAL TUBULAR ACIDOSIS, DISTAL, 4, WITH HEMOLYTIC ANEMIA",,,,,,,C5436235,,109270;611590,MONDO:0012700,"renal tubular acidosis, distal, 4, with hemolytic anemia",
+BMGC_DS18154,BMG_DS069719,,RAJAB INTERSTITIAL LUNG DISEASE WITH BRAIN CALCIFICATIONS 1,,,,,,,C5436276,,618007;613658;609690;613658,MONDO:0100215,Rajab interstitial lung disease with brain calcifications 1,
+BMGC_DS18155,BMG_DS069720,,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 6,,,,,DOID:0060205,frontotemporal dementia and/or amyotrophic lateral sclerosis 6,C5436279,,613954;601023,MONDO:0013501,frontotemporal dementia and/or amyotrophic lateral sclerosis 6,
+BMGC_DS18156,BMG_DS069721,,"MENTAL RETARDATION, AUTOSOMAL DOMINANT 25, FORMERLY",,,,,DOID:0070055,Xia-Gibbs Syndrome,C5436345,,615829,,,
+BMGC_DS18157,BMG_DS069722,,ARTHROGRYPOSIS MULTIPLEX CONGENITA 5,,,,,DOID:0080981,arthrogryposis multiplex congenita-5,C5436453,,605204;618947,MONDO:0100218,arthrogryposis multiplex congenita 5,
+BMGC_DS18158,BMG_DS069723,,SULEIMAN-EL-HATTAB SYNDROME,,,,,,,C5436458,,608270;618950,MONDO:0033532,Suleiman-El-Hattab syndrome,
+BMGC_DS18159,BMG_DS069724,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 45,,,,,DOID:0112113,combined oxidative phosphorylation deficiency 45,C5436461,,618951;602375,MONDO:0033533,combined oxidative phosphorylation deficiency 45,
+BMGC_DS18160,BMG_DS069725,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 46,,,,,DOID:0112115,combined oxidative phosphorylation deficiency 46,C5436466,,611985;618952,MONDO:0033534,combined oxidative phosphorylation deficiency 46,
+BMGC_DS18161,BMG_DS069726,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 47,,,,,DOID:0112114,combined oxidative phosphorylation deficiency 47,C5436476,,611990;618958,MONDO:0033537,combined oxidative phosphorylation deficiency 47,
+BMGC_DS18162,BMG_DS069727,,IMMUNODEFICIENCY 69,,,,,DOID:0112006,immunodeficiency 69,C5436498,,618963;147570,MONDO:0033541,immunodeficiency 69,
+BMGC_DS18163,BMG_DS069728,,IMMUNODEFICIENCY 70,,,,,DOID:0112005,immunodeficiency 70,C5436501,,609209;618969,MONDO:0033542,immunodeficiency 70,
+BMGC_DS18164,BMG_DS069729,,"CONE-ROD SYNAPTIC DISORDER SYNDROME, CONGENITAL NONPROGRESSIVE",,,,,,,C5436505,,606630;618970,MONDO:0033543,"cone-rod synaptic disorder syndrome, congenital nonprogressive",
+BMGC_DS18165,BMG_DS069730,,TOLCHIN-LE CAIGNEC SYNDROME,,,,,,,C5436509,,607257;618971,MONDO:0033544,Tolchin-Le Caignec syndrome,
+BMGC_DS18166,BMG_DS069731,,MITOCHONDRIAL DNA DEPLETION SYNDROME 19,,,,,DOID:0070450,mitochondrial DNA depletion syndrome 19,C5436514,,618972;606794,MONDO:0033545,mitochondrial DNA depletion syndrome 19,
+BMGC_DS18167,BMG_DS069732,,SODIUM-DEPENDENT MULTIVITAMIN TRANSPORTER DEFICIENCY,,,,,,,C5436520,,618973;604024,MONDO:0033546,"neurodegeneration, infantile-onset, biotin-responsive",
+BMGC_DS18168,BMG_DS069733,,LI-GHORBANI-WEISZ-HUBSHMAN SYNDROME,,,,,,,C5436525,,618974;609912,MONDO:0033547,Li-Ghorbani-Weisz-Hubshman syndrome,
+BMGC_DS18169,BMG_DS069734,,"MYOPATHY, CONGENITAL, WITH DIAPHRAGMATIC DEFECTS, RESPIRATORY INSUFFICIENCY, AND DYSMORPHIC FACIES",,,,,DOID:0081349,congenital myopathy 17,C5436530,,618975,MONDO:0033548,"myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies",
+BMGC_DS18170,BMG_DS069735,,OPTIC ATROPHY 12,,,,,DOID:0080840,optic atrophy 12,C5436534,,604581;618977,MONDO:0033549,optic atrophy 12,
+BMGC_DS18171,BMG_DS069736,,IMMUNODEFICIENCY 72 WITH AUTOINFLAMMATION AND LYMPHOPROLIFERATION,,,,,DOID:0112015,immunodeficiency 72,C5436540,,141180;618982,MONDO:0033551,immunodeficiency 72 with autoinflammation,
+BMGC_DS18172,BMG_DS069737,,"GROWTH HORMONE INSENSITIVITY SYNDROME WITH IMMUNE DYSREGULATION 2, AUTOSOMAL DOMINANT",,,,,DOID:0080837,growth hormone insensitivity syndrome with immune dysregulation 2,C5436546,,618985;604260,MONDO:0100219,"growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant",
+BMGC_DS18173,BMG_DS069738,,IMMUNODEFICIENCY 73B WITH DEFECTIVE NEUTROPHIL CHEMOTAXIS AND LYMPHOPENIA,,,,,DOID:0112061,immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia,C5436549,,618986;602049,MONDO:0033554,immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia,
+BMGC_DS18174,BMG_DS069739,,IMMUNODEFICIENCY 73C WITH DEFECTIVE NEUTROPHIL CHEMOTAXIS AND HYPOGAMMAGLOBULINEMIA,,,,,DOID:0112062,immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia,C5436550,,602049;618987,MONDO:0033555,immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia,
+BMGC_DS18175,BMG_DS069740,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 15",,,,,DOID:0112376,muscular dystrophy-dystroglycanopathy type B15,C5436552,,605951;618992,MONDO:0033556,"muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15",
+BMGC_DS18176,BMG_DS069741,,IMMUNE DYSREGULATION AND SYSTEMIC HYPERINFLAMMATION SYNDROME,,,,,,,C5436563,,609424;618998,MONDO:0033557,"hemophagocytic lymphohistiocytosis, familial, 6",
+BMGC_DS18177,BMG_DS069742,,"AUTOINFLAMMATION, IMMUNE DYSREGULATION, AND EOSINOPHILIA",,,,,,,C5436572,,147795;618999,MONDO:0033558,"autoinflammation, immune dysregulation, and eosinophilia",
+BMGC_DS18178,BMG_DS069743,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEIZURES AND LANGUAGE DELAY,,,,,,,C5436574,,611055;619000,MONDO:0033559,intellectual developmental disorder with seizures and language delay,
+BMGC_DS18179,BMG_DS069744,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 35",,,,,DOID:0112139,nuclear type mitochondrial complex I deficiency 35,C5436576,,619003;603843,MONDO:0033560,"mitochondrial complex 1 deficiency, nuclear type 35",
+BMGC_DS18180,BMG_DS069745,,DEEAH SYNDROME,,,,,,,C5436579,,603584;619004,MONDO:0033561,deeah syndrome,
+BMGC_DS18181,BMG_DS069746,,"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA",,,,,,,C5436585,,603584;619005,MONDO:0033562,"neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotonia",
+BMGC_DS18182,BMG_DS069747,,RETINITIS PIGMENTOSA 90,,,,,DOID:0112147,retinitis pigmentosa 90,C5436588,,619007;601149,MONDO:0033563,retinitis pigmentosa 90,
+BMGC_DS18183,BMG_DS069748,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 8,,,,,,,C5436597,,605673;619009,MONDO:0033564,oocyte maturation defect 8,
+BMGC_DS18184,BMG_DS069749,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 9,,,,,,,C5436599,,619011;604507,MONDO:0033565,oocyte maturation defect 9,
+BMGC_DS18185,BMG_DS069750,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 48,,,,,DOID:0112112,combined oxidative phosphorylation deficiency 48,C5436602,,619012;617491,MONDO:0033566,combined oxidative phosphorylation deficiency 48,
+BMGC_DS18186,BMG_DS069751,,RAJAB INTERSTITIAL LUNG DISEASE WITH BRAIN CALCIFICATIONS 2,,,,,,,C5436603,,602918;619013,MONDO:0100220,Rajab interstitial lung disease with brain calcifications 2,
+BMGC_DS18187,BMG_DS069752,,IFAP SYNDROME 2,,,,,,,C5436607,,619016;184756,MONDO:0100221,IFAP syndrome 2,
+BMGC_DS18188,BMG_DS069753,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 49,,,,,DOID:0112110,combined oxidative phosphorylation deficiency 49,C5436616,,619024;615498,MONDO:0033569,combined oxidative phosphorylation deficiency 49,
+BMGC_DS18189,BMG_DS069754,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 50,,,,,DOID:0112111,combined oxidative phosphorylation deficiency 50,C5436623,,619025;611987,MONDO:0033570,combined oxidative phosphorylation deficiency 50,
+BMGC_DS18190,BMG_DS069755,,NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE SPASTICITY AND BRAIN WHITE MATTER ABNORMALITIES,,,,,,,C5436628,,618994;619026;603513;619026,MONDO:0033613,neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities,
+BMGC_DS18191,BMG_DS069756,,"SPASTIC PARAPLEGIA 83, AUTOSOMAL RECESSIVE",,,,,DOID:0112346,hereditary spastic paraplegia 83,C5436637,,618994;619027,MONDO:0033614,"spastic paraplegia 83, autosomal recessive",
+BMGC_DS18192,BMG_DS069757,,"COENZYME Q10 DEFICIENCY, PRIMARY, 9",,,,,DOID:0112138,primary coenzyme Q10 deficiency 9,C5436638,,619028;616359,MONDO:0033615,"coenzyme q10 deficiency, primary, 9",
+BMGC_DS18193,BMG_DS069758,,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH EPILEPSY, BEHAVIORAL ABNORMALITIES, AND COARSE FACIES",,,,,,,C5436646,,619031;612866,MONDO:0033572,"intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies",
+BMGC_DS18194,BMG_DS069759,,VISSERS-BODMER SYNDROME,,,,,DOID:0081397,Vissers-Bodmer syndrome,C5436647,,604917;619033,MONDO:0033618,Vissers-Bodmer syndrome,
+BMGC_DS18195,BMG_DS069760,,"MYOPATHY, EPILEPSY, AND PROGRESSIVE CEREBRAL ATROPHY",,,,,,,C5436652,,612866;619036,MONDO:0033619,"myopathy, epilepsy, and progressive cerebral atrophy",
+BMGC_DS18196,BMG_DS069761,,MYOFIBRILLAR MYOPATHY 10,,,,,DOID:0112108,myofibrillar myopathy 10,C5436656,,619040;604126,MONDO:0033620,myofibrillar myopathy 10,
+BMGC_DS18197,BMG_DS069762,,MONOSOMY 7 MYELODYSPLASIA AND LEUKEMIA SYNDROME 2,,,,,,,C5436668,,619041;610456,MONDO:0030801,monosomy 7 myelodysplasia and leukemia syndrome 2,
+BMGC_DS18198,BMG_DS069763,,"SPINAL MUSCULAR ATROPHY, INFANTILE, JAMES TYPE",,,,,,,C5436669,,619042;600287,MONDO:0033621,"spinal muscular atrophy, infantile, James type",
+BMGC_DS18199,BMG_DS069764,,SPERMATOGENIC FAILURE 44,,,,,DOID:0112109,spermatogenic failure 44,C5436678,,619044;618980,MONDO:0033622,spermatogenic failure 44,
+BMGC_DS18200,BMG_DS069765,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 3",,,,,DOID:0070492,mitochondrial complex IV deficiency nuclear type 3,C5436682,,602125;619046,MONDO:0033635,"mitochondrial complex 4 deficiency, nuclear type 3",
+BMGC_DS18201,BMG_DS069766,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 4",,,,,DOID:0070493,mitochondrial complex IV deficiency nuclear type 4,C5436683,,603644;619048,MONDO:0033636,"mitochondrial complex 4 deficiency, nuclear type 4",
+BMGC_DS18202,BMG_DS069767,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 7",,,,,DOID:0070494,mitochondrial complex IV deficiency nuclear type 7,C5436685,,124089;619051,MONDO:0033637,"mitochondrial complex 4 deficiency, nuclear type 7",
+BMGC_DS18203,BMG_DS069768,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 8",,,,,DOID:0070495,mitochondrial complex IV deficiency nuclear type 8,C5436689,,619052;612958,MONDO:0033638,"mitochondrial complex 4 deficiency, nuclear type 8",
+BMGC_DS18204,BMG_DS069769,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 10",,,,,DOID:0070496,mitochondrial complex IV deficiency nuclear type 10,C5436692,,614478;619053,MONDO:0033639,"mitochondrial complex 4 deficiency, nuclear type 10",
+BMGC_DS18205,BMG_DS069770,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 11",,,,,DOID:0070497,mitochondrial complex IV deficiency nuclear type 11,C5436694,,614698;619054,MONDO:0033645,"mitochondrial complex 4 deficiency, nuclear type 11",
+BMGC_DS18206,BMG_DS069771,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 12",,,,,DOID:0070498,mitochondrial complex IV deficiency nuclear type 12,C5436695,,614770;619055,MONDO:0033646,"mitochondrial complex 4 deficiency, nuclear type 12",
+BMGC_DS18207,BMG_DS069772,,NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES,,,,,DOID:0070417,neurodevelopmental disorder with speech impairment and dysmorphic facies,C5436699,,611052;619056,MONDO:0033630,neurodevelopmental disorder with speech impairment and dysmorphic facies,
+BMGC_DS18208,BMG_DS069773,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 51,,,,,DOID:0112137,combined oxidative phosphorylation deficiency 51,C5436703,,614918;619057,MONDO:0033631,combined oxidative phosphorylation deficiency 51,
+BMGC_DS18209,BMG_DS069774,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 14",,,,,DOID:0070499,mitochondrial complex IV deficiency nuclear type 14,C5436710,,614775;619058,MONDO:0033649,"mitochondrial complex 4 deficiency, nuclear type 14",
+BMGC_DS18210,BMG_DS069775,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 15",,,,,DOID:0070500,mitochondrial complex IV deficiency nuclear type 15,C5436712,,123870;619059,MONDO:0033650,"mitochondrial complex 4 deficiency, nuclear type 15",
+BMGC_DS18211,BMG_DS069776,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 16",,,,,DOID:0070501,mitochondrial complex IV deficiency nuclear type 16,C5436714,,619060;123864,MONDO:0033651,"mitochondrial complex 4 deficiency, nuclear type 16",
+BMGC_DS18212,BMG_DS069777,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 17",,,,,DOID:0070502,mitochondrial complex IV deficiency nuclear type 17,C5436718,,619061;616003,MONDO:0033652,"mitochondrial complex 4 deficiency, nuclear type 17",
+BMGC_DS18213,BMG_DS069778,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 18",,,,,DOID:0070503,mitochondrial complex IV deficiency nuclear type 18,C5436720,,619062;602009,MONDO:0033653,"mitochondrial complex 4 deficiency, nuclear type 18",
+BMGC_DS18214,BMG_DS069779,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 19",,,,,DOID:0070504,mitochondrial complex IV deficiency nuclear type 19,C5436723,,614771;619063,MONDO:0033654,"mitochondrial complex 4 deficiency, nuclear type 19",
+BMGC_DS18215,BMG_DS069780,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 20",,,,,DOID:0070505,mitochondrial complex IV deficiency nuclear type 20,C5436726,,603773;619064,MONDO:0033655,"mitochondrial complex 4 deficiency, nuclear type 20",
+BMGC_DS18216,BMG_DS069781,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 21",,,,,DOID:0070506,mitochondrial complex IV deficiency nuclear type 21,C5436727,,603833;619065,MONDO:0033656,"mitochondrial complex 4 deficiency, nuclear type 21",
+BMGC_DS18217,BMG_DS069782,,"LEUKODYSTROPHY, HYPOMYELINATING, 20",,,,,DOID:0112153,hypomyelinating leukodystrophy 20,C5436730,,123830;619071,MONDO:0033657,"leukodystrophy, hypomyelinating, 20",
+BMGC_DS18218,BMG_DS069783,,NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ATROPHY,,,,,,,C5436732,,608163;619072,MONDO:0033658,neurodevelopmental disorder with seizures and brain atrophy,
+BMGC_DS18219,BMG_DS069784,,"VITAMIN D-DEPENDENT RICKETS, TYPE 3",,,,,,,C5436733,,619073;124010,MONDO:0033640,"vitamin D-dependent rickets, type 3",
+BMGC_DS18220,BMG_DS069785,,"CLEFT PALATE, PROLIFERATIVE RETINOPATHY, AND DEVELOPMENTAL DELAY",,,,,,,C5436739,,137207;619074,MONDO:0033641,"cleft palate, proliferative retinopathy, and developmental delay",
+BMGC_DS18221,BMG_DS069786,1222658006,"Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome",,,,,,,C5436741,,619075,MONDO:0033642,neurodevelopmental disorder with alopecia and brain abnormalities,"Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome | Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome (disorder) | Bachmann Bupp syndrome | Ornithine decarboxylase deficiency"
+BMGC_DS18222,BMG_DS069787,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND BRAIN ATROPHY",,,,,,,C5436747,,615283;619076,MONDO:0033662,"neurodevelopmental disorder with microcephaly, seizures, and brain atrophy",
+BMGC_DS18223,BMG_DS069788,,INFLAMMATORY BOWEL DISEASE (CROHN DISEASE) 30,,,,,DOID:0112154,inflammatory bowel disease 30,C5436750,,609051;619079,MONDO:0033643,inflammatory bowel disease 30,
+BMGC_DS18224,BMG_DS069789,,KILQUIST SYNDROME,,,,,,,C5436756,,619080;600840,MONDO:0033664,Kilquist syndrome,
+BMGC_DS18225,BMG_DS069790,,"DEAFNESS, AUTOSOMAL DOMINANT 78",,,,,DOID:0112159,autosomal dominant nonsyndromic deafness 78,C5436768,,600840;619081,MONDO:0033665,"hearing loss, autosomal dominant 78",
+BMGC_DS18226,BMG_DS069791,,"MICROCORNEA, ROD-CONE DYSTROPHY, CATARACT, AND POSTERIOR STAPHYLOMA 1",,,,,,,C5436769,,619082;601175,MONDO:0033644,"microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1",
+BMGC_DS18227,BMG_DS069792,,DELPIRE-MCNEILL SYNDROME,,,,,,,C5436771,,619083;600840,MONDO:0033667,Delpire-McNeill syndrome,
+BMGC_DS18228,BMG_DS069793,,"DEAFNESS, AUTOSOMAL DOMINANT 79",,,,,DOID:0112160,autosomal dominant nonsyndromic deafness 79,C5436772,,608370;619086,MONDO:0033668,"hearing loss, autosomal dominant 79",
+BMGC_DS18229,BMG_DS069794,,NOONAN SYNDROME 13,,,,,DOID:0112161,Noonan syndrome 13,C5436773,,176948;619087,MONDO:0033669,Noonan syndrome 13,
+BMGC_DS18230,BMG_DS069795,,"DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY",,,,,,,C5436781,,619090;616661,MONDO:0030835,"developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy",
+BMGC_DS18231,BMG_DS069796,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, IMPAIRED LANGUAGE, AND GAIT ABNORMALITIES",,,,,,,C5436783,,108410;619091,MONDO:0100348,"neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities",
+BMGC_DS18232,BMG_DS069797,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, IMPAIRED LANGUAGE, EPILEPSY, AND GAIT ABNORMALITIES",,,,,,,C5436788,,108410;619092,MONDO:0030837,"neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities",
+BMGC_DS18233,BMG_DS069798,,"DEAFNESS, AUTOSOMAL RECESSIVE 116",,,,,DOID:0112162,autosomal recessive nonsyndromic deafness 116,C5436789,,615799;619093,MONDO:0033670,"hearing loss, autosomal recessive 116",
+BMGC_DS18234,BMG_DS069799,,SPERMATOGENIC FAILURE 45,,,,,DOID:0112163,spermatogenic failure 45,C5436791,,619094;603333,MONDO:0033671,spermatogenic failure 45,
+BMGC_DS18235,BMG_DS069800,,SPERMATOGENIC FAILURE 46,,,,,DOID:0112164,spermatogenic failure 46,C5436799,,619095;603337,MONDO:0033673,spermatogenic failure 46,
+BMGC_DS18236,BMG_DS069801,,mismatch repair cancer syndrome 2,,,,,,,C5436806,C536928,619096,MONDO:0030840,mismatch repair cancer syndrome 2,
+BMGC_DS18237,BMG_DS069802,,mismatch repair cancer syndrome 3,,,,,,,C5436807,C536928,619097,MONDO:0030841,mismatch repair cancer syndrome 3,
+BMGC_DS18238,BMG_DS069803,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY AND AXONAL PERIPHERAL NEUROPATHY,,,,,,,C5436813,,619099;608378,MONDO:0030849,intellectual developmental disorder with speech delay and axonal peripheral neuropathy,
+BMGC_DS18239,BMG_DS069804,,mismatch repair cancer syndrome 4,,,,,,,C5436817,C536928,619101,MONDO:0030843,mismatch repair cancer syndrome 4,
+BMGC_DS18240,BMG_DS069805,,SPERMATOGENIC FAILURE 47,,,,,DOID:0112175,spermatogenic failure 47,C5436818,,619102;608671,MONDO:0030844,spermatogenic failure 47,
+BMGC_DS18241,BMG_DS069806,,"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES",,,,,,,C5436821,,619103;601409,MONDO:0030852,"neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities",
+BMGC_DS18242,BMG_DS069807,,SPERMATOGENIC FAILURE 48,,,,,DOID:0112176,spermatogenic failure 48,C5436823,,619098;619108,MONDO:0030846,spermatogenic failure 48,
+BMGC_DS18243,BMG_DS069808,,"ARTHROGRYPOSIS, DISTAL, TYPE 1C",,,,,DOID:0112190,distal arthrogryposis type 1C,C5436834,,617378;619110,MONDO:0030847,"arthrogryposis, distal, type 1C",
+BMGC_DS18244,BMG_DS069809,,COACH SYNDROME 2,,,,,,,C5436837,,619111;612013,MONDO:0030859,COACH syndrome 2,
+BMGC_DS18245,BMG_DS069810,,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 13",,,,,DOID:0081401,autosomal dominant distal hereditary motor neuronopathy 13,C5436838,,619112;606158,MONDO:0030860,"neuronopathy, distal hereditary motor, type 5C",
+BMGC_DS18246,BMG_DS069811,,COACH SYNDROME 3,,,,,,,C5436841,,610937;619113,MONDO:0030862,COACH syndrome 3,
+BMGC_DS18247,BMG_DS069812,,COMBINED OSTEOGENESIS IMPERFECTA AND EHLERS-DANLOS SYNDROME 1,,,,,,,C5436842,,120150;619115,MONDO:0030854,combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1,
+BMGC_DS18248,BMG_DS069813,,COMBINED OSTEOGENESIS IMPERFECTA AND EHLERS-DANLOS SYNDROME 2,,,,,,,C5436847,,120160;619120,MONDO:0030855,combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2,
+BMGC_DS18249,BMG_DS069814,,"NEURODEVELOPMENTAL DISORDER WITH CARDIOMYOPATHY, SPASTICITY, AND BRAIN ABNORMALITIES",,,,,DOID:0070543,"neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities",C5436848,,619121;138450,MONDO:0030866,"neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities",
+BMGC_DS18250,BMG_DS069815,,VERTEBRAL HYPERSEGMENTATION AND OROFACIAL ANOMALIES,,,,,DOID:0070418,vertebral hypersegmentation and orofacial anomalies,C5436851,,619122;603936,MONDO:0030871,vertebral hypersegmentation and orofacial anomalies,
+BMGC_DS18251,BMG_DS069816,,CARDIOFACIONEURODEVELOPMENTAL SYNDROME,,,,,,,C5436852,,618941;619123,MONDO:0030873,cardiofacioneurodevelopmental syndrome,
+BMGC_DS18252,BMG_DS069817,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 89,,,,,DOID:0112223,developmental and epileptic encephalopathy 89,C5436853,,605363;619124,MONDO:0030856,developmental and epileptic encephalopathy 89,
+BMGC_DS18253,BMG_DS069818,,KAYA-BARAKAT-MASSON SYNDROME,,,,,,,C5436856,,619125;619109,MONDO:0030878,Kaya-Barakat-Masson syndrome,
+BMGC_DS18254,BMG_DS069819,,IMMUNODEFICIENCY 75 WITH LYMPHOPROLIFERATION,,,,,,,C5436860,,619126;612839,MONDO:0030858,immunodeficiency 75,
+BMGC_DS18255,BMG_DS069820,,MANDIBULOACRAL DYSPLASIA PROGEROID SYNDROME,,,,,,,C5436867,,608555;619127,MONDO:0030880,mandibuloacral dysplasia progeroid syndrome,
+BMGC_DS18256,BMG_DS069821,,THROMBOCYTOPENIA 7,,,,,,,C5436874,,619130;606238,MONDO:0030867,thrombocytopenia 7,
+BMGC_DS18257,BMG_DS069822,,"OSTEOGENESIS IMPERFECTA, TYPE XXI",,,,,DOID:0112201,osteogenesis imperfecta type 21,C5436875,,619131;609024,MONDO:0030861,"osteogenesis imperfecta, type 21",
+BMGC_DS18258,BMG_DS069823,,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 8,,,,,,,C5436881,,605018;619132,MONDO:0030872,frontotemporal dementia and/or amyotrophic lateral sclerosis 8,
+BMGC_DS18259,BMG_DS069824,,AMYOTROPHIC LATERAL SCLEROSIS 26 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA,,,,,DOID:0081380,amyotrophic lateral sclerosis type 26,C5436882,,603518;619133,MONDO:0030885,amyotrophic lateral sclerosis 26 with or without frontotemporal dementia,
+BMGC_DS18260,BMG_DS069825,,RITSCHER-SCHINZEL SYNDROME 3,,,,,,,C5436883,,618981;619135,MONDO:0030864,Ritscher-Schinzel syndrome 3,
+BMGC_DS18261,BMG_DS069826,,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 5,,,,,,,C5436884,,600227;619141,MONDO:0030875,frontotemporal dementia and/or amyotrophic lateral sclerosis 5,
+BMGC_DS18262,BMG_DS069827,,CARDIOACROFACIAL DYSPLASIA 1,,,,,,,C5436885,,619142;601639,MONDO:0030876,cardioacrofacial dysplasia 1,
+BMGC_DS18263,BMG_DS069828,,CARDIOACROFACIAL DYSPLASIA 2,,,,,,,C5436886,,176892;619143,MONDO:0030877,cardioacrofacial dysplasia 2,
+BMGC_DS18264,BMG_DS069829,,SPERMATOGENIC FAILURE 49,,,,,DOID:0112271,spermatogenic failure 49,C5436887,,619129;619144,MONDO:0030868,spermatogenic failure 49,
+BMGC_DS18265,BMG_DS069830,,SPERMATOGENIC FAILURE 50,,,,,DOID:0112272,spermatogenic failure 50,C5436888,,600375;619145,MONDO:0030869,spermatogenic failures 50,
+BMGC_DS18266,BMG_DS069831,,PREMATURE OVARIAN FAILURE 17,,,,,DOID:0080874,primary ovarian insufficiency 17,C5436889,,600375;619146,MONDO:0030870,premature ovarian failure 17,
+BMGC_DS18267,BMG_DS069832,,CHROMOSOME 13q33-q34 DELETION SYNDROME,,,,,,,C5436890,,619148,MONDO:0030896,chromosome 13q33-q34 deletion syndrome,
+BMGC_DS18268,BMG_DS069833,,LESSEL-KREIENKAMP SYNDROME,,,,,,,C5436892,,606229;619149,MONDO:0030897,Lessel-Kreienkamp syndrome,
+BMGC_DS18269,BMG_DS069834,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH PAROXYSMAL DYSKINESIA OR SEIZURES,,,,,,,C5436894,,619150;602658,MONDO:0030900,intellectual developmental disorder with paroxysmal dyskinesia or seizures,
+BMGC_DS18270,BMG_DS069836,1332385000,AMeD syndrome,,,,,,,C5436906,,619151,MONDO:0030894,"AMED syndrome, digenic","Aplastic anemia, intellectual disability, dwarfism syndrome | AMeD syndrome | AMeD (aplastic anemia, intellectual disability, dwarfism) syndrome | Aplastic anaemia, intellectual disability, dwarfism syndrome | Aplastic anemia, intellectual disability, dwarfism syndrome (disorder) | AMeD (aplastic anaemia, intellectual disability, dwarfism) syndrome"
+BMGC_DS18271,BMG_DS069837,,"NEPHROTIC SYNDROME, TYPE 22",,,,,DOID:0112268,nephrotic syndrome type 22,C5436909,,619155;605551,MONDO:0030895,"nephrotic syndrome, type 22",
+BMGC_DS18272,BMG_DS069838,,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT EARLY-ONSET GENERALIZED EPILEPSY,,,,,,,C5436914,,619157,MONDO:0030930,neurodevelopmental disorder with or without early-onset generalized epilepsy,
+BMGC_DS18273,BMG_DS069839,,CARPAL TUNNEL SYNDROME 2,,,,,DOID:0070467,carpal tunnel syndrome 2,C5436916,,600310;619161,MONDO:0030883,carpal tunnel syndrome 2,
+BMGC_DS18274,BMG_DS069840,1300116006,Oculocutaneous albinism type 8,,,,,,,C5436929,,619165,MONDO:0030899,oculocutaneous albinism type 8,Oculocutaneous albinism type 8 (disorder) | Oculocutaneous albinism type 8 | OCA8 - oculocutaneous albinism type 8
+BMGC_DS18275,BMG_DS069841,,"MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 2",,,,,,,C5436933,,612848;619166,MONDO:0030935,"mitochondrial complex 2 deficiency, nuclear type 2",
+BMGC_DS18276,BMG_DS069842,,"MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 3",,,,,,,C5436934,,602690;619167,MONDO:0030937,"mitochondrial complex 2 deficiency, nuclear type 3",
+BMGC_DS18277,BMG_DS069843,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 36",,,,,,,C5436935,,603845;619170,MONDO:0030902,"mitochondrial complex 1 deficiency, nuclear type 36",
+BMGC_DS18278,BMG_DS069844,,HERMANSKY-PUDLAK SYNDROME 11,,,,,,,C5436936,,619172;607289,MONDO:0030903,Hermansky-Pudlak syndrome 11,
+BMGC_DS18279,BMG_DS069845,,"DEAFNESS, AUTOSOMAL RECESSIVE 117",,,,,,,C5436937,,618988;619174,MONDO:0030905,"hearing loss, autosomal recessive 117",
+BMGC_DS18280,BMG_DS069846,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 10,,,,,,,C5436938,,618421;619176,MONDO:0030925,oocyte maturation defect 10,
+BMGC_DS18281,BMG_DS069861,,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 1",,,,,DOID:0050588,muscular dystrophy-dystroglycanopathy type B1,C5436962,,607423;613155,MONDO:0013159,"muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1",
+BMGC_DS18282,BMG_DS069995,880066000,Alpha-N-acetylgalactosaminidase deficiency type 3,,,,,,,C5437471,,,MONDO:0019264,alpha-N-acetylgalactosaminidase deficiency type 3,Alpha-N-acetylgalactosaminidase deficiency type 3 (disorder) | Alpha-N-acetylgalactosaminidase deficiency type 3 | Schindler disease type 3 | NAGA (alpha-N-acetylgalactosaminidase) deficiency type 3
+BMGC_DS18283,BMG_DS070023,200824008,Contact dermatitis caused by urushiol from poison oak,,,,,,,C5437556,,,,,Contact dermatitis caused by poison oak | Contact dermatitis caused by urushiol from poison oak (disorder) | Contact dermatitis caused by urushiol from poison oak
+BMGC_DS18284,BMG_DS070042,890180006,Blepharophimosis epicanthus inversus ptosis syndrome plus,,,,,,,C5437588,,,MONDO:0035521,blepharophimosis-ptosis-epicanthus inversus syndrome plus,3q23 microdeletion syndrome | Blepharophimosis epicanthus inversus ptosis syndrome plus (disorder) | Blepharophimosis epicanthus inversus ptosis syndrome plus | BPES (blepharophimosis epicanthus inversus ptosis syndrome) plus
+BMGC_DS18285,BMG_DS070045,,,,,,,,,C5437603,,,MONDO:0800188,"malignant hyperthermia, susceptibility to",
+BMGC_DS18286,BMG_DS070052,890118006,Mowat-Wilson syndrome due to monosomy 2q22,,,,,,,C5437617,,,MONDO:0016855,Mowat-Wilson syndrome due to monosomy 2q22,Hirschsprung disease and intellectual disability due to del(2)(q22) | Hirschsprung disease and intellectual disability due to monosomy 2q22 | Mowat-Wilson syndrome due to monosomy 2q22 (disorder) | Hirschsprung disease and intellectual disability due to 2q22 microdeletion | Mowat-Wilson syndrome due to del(2)q(22) | Mowat-Wilson syndrome due to monosomy 2q22 | Mowat-Wilson syndrome due to 2q22 microdeletion
+BMGC_DS18287,BMG_DS070067,890235002,Autosomal recessive epidermolytic ichthyosis,,,,,,,C5437635,,,MONDO:0044742,autosomal recessive epidermolytic ichthyosis,Autosomal recessive epidermolytic ichthyosis (disorder) | Autosomal recessive epidermolytic ichthyosis
+BMGC_DS18288,BMG_DS070144,,,,,,,,,C5437887,,,MONDO:0020360,complete cryptophthalmia,
+BMGC_DS18289,BMG_DS070240,1003380001,6q16 microdeletion syndrome,,,,,,,C5438727,,,MONDO:0015749,6q16 deletion syndrome,Prader-Willi-like syndrome due to microdeletion 6q16 | 6q16 microdeletion syndrome | 6q16 microdeletion syndrome (disorder) | Obesity due to 6q16 deletion
+BMGC_DS18290,BMG_DS070248,1003877009,Pfeiffer syndrome type 1,,,,,,,C5438812,,,MONDO:0019659,Pfeiffer syndrome type 1,Pfeiffer syndrome type 1 (disorder) | Pfeiffer syndrome type 1
+BMGC_DS18291,BMG_DS070249,1003881009,Pelizaeus-Merzbacher disease in female carrier,,,,,,,C5438815,,,MONDO:0017224,Pelizaeus-Merzbacher disease in female carriers,Pelizaeus-Merzbacher disease in female carrier | Pelizaeus-Merzbacher disease in female carrier (disorder)
+BMGC_DS18292,BMG_DS070250,1003916008,Pfeiffer syndrome type 2,,,,,,,C5438849,,,MONDO:0019660,Pfeiffer syndrome type 2,Pfeiffer syndrome type 2 (disorder) | Pfeiffer syndrome type 2
+BMGC_DS18293,BMG_DS070251,1003918009,Pfeiffer syndrome type 3,,,,,,,C5438850,,,MONDO:0019661,Pfeiffer syndrome type 3,Pfeiffer syndrome type 3 (disorder) | Pfeiffer syndrome type 3
+BMGC_DS18294,BMG_DS070281,1003437009,Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation,,,,,,,C5438974,,,MONDO:0019930,Leydig cell hypoplasia due to complete LH resistance,Leydig cell hypoplasia due to complete LH receptor inactivation | Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) | Leydig cell hypoplasia due to complete luteinising hormone receptor inactivation | Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation
+BMGC_DS18295,BMG_DS070282,1003438004,Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation,,,,,,,C5438975,,,MONDO:0019931,Leydig cell hypoplasia due to partial LH resistance,Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation | Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation | Leydig cell hypoplasia due to partial LH receptor inactivation | Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation (disorder)
+BMGC_DS18296,BMG_DS070333,1010666007,Stickler syndrome type 4,,,,,,,C5439212,,,,,Stickler syndrome type 4 (disorder) | Stickler syndrome type 4 | Autosomal recessive Stickler syndrome
+BMGC_DS18297,BMG_DS070379,1003447007,Pelizaeus-Merzbacher disease null syndrome,,,,,,,C5439441,,,MONDO:0017225,null syndrome,PLP1 null syndrome | Null syndrome | Pelizaeus-Merzbacher disease null syndrome | Pelizaeus-Merzbacher disease null syndrome (disorder)
+BMGC_DS18298,BMG_DS070407,,Enteric Neuropathy,Intestinal Pseudo-Obstruction,,,,,,C5441716,D007418,,,,
+BMGC_DS18299,BMG_DS070408,715201005,Congenital short bowel syndrome,,,,,,,C5441717,,,MONDO:0014097,congenital short bowel syndrome,Congenital short bowel syndrome (disorder) | Congenital short bowel syndrome
+BMGC_DS18300,BMG_DS070410,,,,,,,,,C5441745,,,MONDO:0015925,interstitial lung disease,
+BMGC_DS18301,BMG_DS070412,,"Diarrhea 3, Secretory Sodium, Congenital",,,,,,,C5441927,C562576,270420,MONDO:0010036,congenital secretory sodium diarrhea 3,
+BMGC_DS18302,BMG_DS070413,,"DIARRHEA 8, SECRETORY SODIUM, CONGENITAL",,,,,,,C5441928,,182307;616868,MONDO:0014808,congenital secretory sodium diarrhea 8,
+BMGC_DS18303,BMG_DS070415,772224009,Warburg micro syndrome,,,,,,,C5442005,,,MONDO:0016649,Warburg micro syndrome,Warburg micro syndrome | Warburg micro syndrome (disorder) | Micro syndrome
+BMGC_DS18304,BMG_DS070416,718610008,Congenital pontocerebellar hypoplasia type 1,,,,,,,C5442006,,,MONDO:0016396,pontocerebellar hypoplasia type 1,Congenital pontocerebellar hypoplasia type 1 (disorder) | Congenital pontocerebellar hypoplasia type 1 | PCH1 - pontocerebellar hypoplasia type 1 | Pontocerebellar hypoplasia type 1 | Norman disease
+BMGC_DS18305,BMG_DS070417,,"BLEEDING DISORDER, PLATELET-TYPE, 16",,,,,,,C5442010,,187800;607759,MONDO:0008552,platelet-type bleeding disorder 16,
+BMGC_DS18306,BMG_DS070418,,"OTOFACIOCERVICAL SYNDROME 2, WITH T-CELL DEFICIENCY",,,,,,,C5442121,,615560,MONDO:0014254,otofaciocervical syndrome 2,
+BMGC_DS18307,BMG_DS070420,,Clonal Cytopenia of Undetermined Significance,,,,,,,C5442191,D000082182,,,,
+BMGC_DS18308,BMG_DS070425,,BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME,,,,,DOID:0081442,blepharophimosis-impaired intellectual development syndrome,C5443984,,619293;600014,MONDO:0859139,blepharophimosis-impaired intellectual development syndrome,
+BMGC_DS18309,BMG_DS070426,,HYPERTRIGLYCERIDEMIA 1,,,,,,,C5444012,,145750,MONDO:0007788,hypertriglyceridemia 1,
+BMGC_DS18310,BMG_DS070427,,COFFIN-SIRIS SYNDROME 12,,,,,DOID:0112370,Coffin-Siris syndrome 12,C5444111,,619325;605690,MONDO:0025699,Coffin-Siris syndrome 12,
+BMGC_DS18311,BMG_DS070428,,"DYSOSTOSIS MULTIPLEX, AIN-NAZ TYPE",,,,,,,C5444223,,619332;619345,MONDO:0859156,"dysostosis multiplex, Ain-Naz type",
+BMGC_DS18312,BMG_DS070429,,"INFLAMMATORY BOWEL DISEASE (INFANTILE ULCERATIVE COLITIS) 31, AUTOSOMAL RECESSIVE",,,,,,,C5444224,,619398,MONDO:0030314,"inflammatory bowel disease (infantile ulcerative colitis) 31, autosomal recessive",
+BMGC_DS18313,BMG_DS070430,,Dentinogenesis Imperfecta 1,Dentinogenesis Imperfecta,,,,,,C5444410,D003811,,,,
+BMGC_DS18314,BMG_DS070435,,,,,,,,,C5445164,,,MONDO:0019190,juvenile polyposis of infancy,
+BMGC_DS18315,BMG_DS070442,,,,,,,,,C5447331,,,MONDO:0028226,autosomal recessive severe congenital neutropenia,
+BMGC_DS18316,BMG_DS070444,1229872004,Xq25 microduplication syndrome,,,,,,,C5447842,,,,,Xq25 microduplication syndrome | Xq25 microtriplication | Xq25 microduplication syndrome (disorder)
+BMGC_DS18317,BMG_DS070445,,,,,,,DOID:5529,lacrimal gland squamous cell carcinoma,C5447980,,,,,
+BMGC_DS18318,BMG_DS070503,,Primary Vesicoureteral Reflux,Vesico-Ureteral Reflux,,,,,,C5539786,D014718,,,,
+BMGC_DS18319,BMG_DS070504,,VENTRICULAR ARRHYTHMIAS DUE TO CARDIAC RYANODINE RECEPTOR CALCIUM RELEASE DEFICIENCY SYNDROME,,,,,,,C5542154,,115000;180902,MONDO:0020745,ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome,
+BMGC_DS18320,BMG_DS070505,,HYPOTAURINEMIC RETINAL DEGENERATION AND CARDIOMYOPATHY,,,,,,,C5542181,,145350;186854,MONDO:0007777,hypotaurinemic retinal degeneration and cardiomyopathy,
+BMGC_DS18321,BMG_DS070506,,VISCERAL MYOPATHY 1,,,,,,,C5542197,,155310;102545,MONDO:0020754,visceral myopathy 1,
+BMGC_DS18322,BMG_DS070507,,ODONTOCHONDRODYSPLASIA 1,,,,,,,C5542277,,604505;184260,MONDO:0100325,odontochondrodysplasia 1,
+BMGC_DS18323,BMG_DS070508,,WHIM SYNDROME 1,,,,,,,C5542296,,162643;193670,MONDO:8000006,WHIM syndrome 1,
+BMGC_DS18324,BMG_DS070509,,MARTSOLF SYNDROME 1,,,,,,,C5542298,,212720;609275,MONDO:8000008,Martsolf syndrome 1,
+BMGC_DS18325,BMG_DS070510,,MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 1,,,,,,,C5542316,,600922;249210,MONDO:0100354,megacystis-microcolon-intestinal hypoperistalsis syndrome 1,
+BMGC_DS18326,BMG_DS070511,,"MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED",,,,,,,C5542341,,301056;300713,MONDO:0025351,"multiple congenital anomalies-neurodevelopmental syndrome, X-linked",
+BMGC_DS18327,BMG_DS070512,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 90,,,,,DOID:0070381,developmental and epileptic encephalopathy 90,C5542345,,301058;300070,MONDO:0025353,"developmental and epileptic encephalopathy, 90",
+BMGC_DS18328,BMG_DS070513,,"SPERMATOGENIC FAILURE, X-LINKED, 3",,,,,DOID:0112274,X-linked spermatogenic failure 3,C5542347,,301059;301057,MONDO:0025354,"spermatogenic failure, X-linked, 3",
+BMGC_DS18329,BMG_DS070514,,"AZOOSPERMIA, OBSTRUCTIVE, WITH NEPHROLITHIASIS",,,,,,,C5542351,,301060;300520,MONDO:0025356,"azoospermia, obstructive, with nephrolithiasis",
+BMGC_DS18330,BMG_DS070516,,"HYPERCHOLANEMIA, FAMILIAL 1",,,,,,,C5542604,,607709;607748,MONDO:0031446,"hypercholanemia, familial 1",
+BMGC_DS18331,BMG_DS070517,,OLMSTED SYNDROME 1,,,,,DOID:0112013,autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques,C5542829,,607066;614594,MONDO:0100296,Olmsted syndrome 1,
+BMGC_DS18332,BMG_DS070518,,"SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES 1",,,,,DOID:0060989,"short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1",C5542952,,112261;617877,MONDO:0100297,"short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1",
+BMGC_DS18333,BMG_DS070519,,"LEUKOENCEPHALOPATHY, PROGRESSIVE, INFANTILE-ONSET, WITH OR WITHOUT DEAFNESS",,,,,,,C5542996,,619147,MONDO:0030893,"leukoencephalopathy, progressive, infantile-onset, with or without deafness",
+BMGC_DS18334,BMG_DS070520,,IMMUNODEFICIENCY 76,,,,,,,C5543004,,613437;619164,MONDO:0030898,immunodeficiency 76,
+BMGC_DS18335,BMG_DS070521,,"NEURODEGENERATION, CHILDHOOD-ONSET, WITH HYPOTONIA, RESPIRATORY INSUFFICIENCY, AND BRAIN IMAGING ABNORMALITIES",,,,,,,C5543020,,619173;602726,MONDO:0030947,"neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities",
+BMGC_DS18336,BMG_DS070522,,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 5,,,,,DOID:0060919,proteosome-associated autoinflammatory syndrome 5,C5543027,,176847;619175,MONDO:0030924,proteasome-associated autoinflammatory syndrome 5,
+BMGC_DS18337,BMG_DS070523,,SPERMATOGENIC FAILURE 51,,,,,DOID:0112273,spermatogenic failure 51,C5543033,,609910;619177,MONDO:0030926,spermatogenic failure 51,
+BMGC_DS18338,BMG_DS070524,,MYOFIBRILLAR MYOPATHY 11,,,,,DOID:0081338,myofibrillar myopathy 11,C5543038,,619178;611220,MONDO:0030927,myofibrillar myopathy 11,
+BMGC_DS18339,BMG_DS070525,,"MICROCEPHALY 26, PRIMARY, AUTOSOMAL DOMINANT",,,,,,,C5543048,,619179;150340,MONDO:0030928,"microcephaly 26, primary, autosomal dominant",
+BMGC_DS18340,BMG_DS070526,,"MICROCEPHALY 27, PRIMARY, AUTOSOMAL DOMINANT",,,,,,,C5543051,,150341;619180,MONDO:0030929,"microcephaly 27, primary, autosomal dominant",
+BMGC_DS18341,BMG_DS070527,,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 4,,,,,DOID:0060915,proteosome-associated autoinflammatory syndrome 4,C5543053,,619183;609702,MONDO:0030931,proteasome-associated autoinflammatory syndrome 4,
+BMGC_DS18342,BMG_DS070528,,"SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES 2",,,,,DOID:0112358,"short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2",C5543057,,614708;619184,MONDO:0030953,"short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2",
+BMGC_DS18343,BMG_DS070529,,JOUBERT SYNDROME 37,,,,,,,C5543064,,617618;619185,MONDO:0030933,Joubert syndrome 37,
+BMGC_DS18344,BMG_DS070530,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 64",,,,,,,C5543067,,616213;619188,MONDO:0030934,"intellectual developmental disorder, autosomal dominant 64",
+BMGC_DS18345,BMG_DS070531,,LI-CAMPEAU SYNDROME,,,,,,,C5543068,,613816;619189,MONDO:0030963,Li-Campeau syndrome,
+BMGC_DS18346,BMG_DS070532,,"EPILEPSY, PROGRESSIVE MYOCLONIC, 12",,,,,,,C5543069,,619192;619191,MONDO:0030936,"epilepsy, progressive myoclonic, 12",
+BMGC_DS18347,BMG_DS070533,,NEUROFACIOSKELETAL SYNDROME WITH OR WITHOUT RENAL AGENESIS,,,,,,,C5543070,,619194,MONDO:0030966,neurofacioskeletal syndrome with or without renal agenesis,
+BMGC_DS18348,BMG_DS070534,,"DEAFNESS, CONGENITAL, AND ADULT-ONSET PROGRESSIVE LEUKOENCEPHALOPATHY",,,,,,,C5543087,,601421;619196,MONDO:0030967,"deafness, congenital, and adult-onset progressive leukoencephalopathy",
+BMGC_DS18349,BMG_DS070536,,"NEPHROTIC SYNDROME, TYPE 23",,,,,DOID:0112266,nephrotic syndrome type 23,C5543092,,607428;619201,MONDO:0030962,"nephrotic syndrome, type 23",
+BMGC_DS18350,BMG_DS070537,,SPERMATOGENIC FAILURE 52,,,,,DOID:0112270,spermatogenic failure 52,C5543094,,617307;619202,MONDO:0030938,spermatogenic failure 52,
+BMGC_DS18351,BMG_DS070538,,PREMATURE OVARIAN FAILURE 18,,,,,DOID:0112269,primary ovarian insufficiency 18,C5543095,,617307;619203,MONDO:0030939,premature ovarian failure 18,
+BMGC_DS18352,BMG_DS070539,,OLMSTED SYNDROME 2,,,,,,,C5543096,,609301;619208,MONDO:0030961,Olmsted syndrome 2,
+BMGC_DS18353,BMG_DS070540,,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 7,,,,,,,C5543106,,609301;619209,MONDO:0030941,erythrokeratodermia variabilis et progressiva 7,
+BMGC_DS18354,BMG_DS070541,,OCULOMOTOR-ABDUCENS SYNKINESIS,,,,,,,C5543116,,610376;619215,MONDO:0030976,oculomotor-abducens synkinesis,
+BMGC_DS18355,BMG_DS070542,,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL RECESSIVE 7",,,,,DOID:0081426,autosomal recessive distal hereditary motor neuronopathy 7,C5543119,,619216;611901,MONDO:0030977,"neuronopathy, distal hereditary motor, autosomal recessive 7",
+BMGC_DS18356,BMG_DS070543,,"ENDOVE SYNDROME, LIMB-ONLY TYPE",,,,,,,C5543128,,619217,MONDO:0030978,"ENDOVE syndrome, limb-only type",
+BMGC_DS18357,BMG_DS070544,,"ENDOVE SYNDROME, LIMB-BRAIN TYPE",,,,,,,C5543142,,131290;619218,MONDO:0030979,"ENDOVE syndrome, limb-brain type",
+BMGC_DS18358,BMG_DS070545,1222681008,"Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome",,,,,,,C5543159,,619220,MONDO:0030971,immunodeficiency 78 with autoimmunity and developmental delay,"Tripeptidyl-peptidase II deficiency | TRIANGLE (TPPII-related immunodeficiency, autoimmunity, neurodevelopmental delay, impaired glycolysis, lysosomal expansion) disease | TPPII-related immunodeficiency, autoimmunity and neurodevelopmental delay with impaired glycolysis and lysosomal expansion disease | Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome (disorder) | Autoimmune haemolytic anaemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome | TPPII (tripeptidyl-peptidase II) deficiency | Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome | Evans syndrome associated with primary immunodeficiency"
+BMGC_DS18359,BMG_DS070546,,SULFIDE:QUINONE OXIDOREDUCTASE DEFICIENCY,,,,,,,C5543168,,617658;619221,MONDO:0030982,sulfide quinone oxidoreductase deficiency,
+BMGC_DS18360,BMG_DS070547,,IMMUNODEFICIENCY 77,,,,,,,C5543173,,610390;619223,MONDO:0030973,immunodeficiency 77,
+BMGC_DS18361,BMG_DS070548,,"MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 4",,,,,,,C5543176,,619224;185470,MONDO:0030974,"mitochondrial complex 2 deficiency, nuclear type 4",
+BMGC_DS18362,BMG_DS070549,,"BLISTERING, ACANTHOLYTIC, OF ORAL AND LARYNGEAL MUCOSA",,,,,,,C5543184,,169615;619226,MONDO:0030986,"blistering, acantholytic, of oral and laryngeal mucosa",
+BMGC_DS18363,BMG_DS070550,,"VERTEBRAL, CARDIAC, TRACHEOESOPHAGEAL, RENAL, AND LIMB DEFECTS",,,,,,,C5543189,,618083;619227,MONDO:0030987,"vertebral, cardiac, tracheoesophageal, renal, and limb defects",
+BMGC_DS18364,BMG_DS070551,,DEVELOPMENTAL DELAY WITH DYSMORPHIC FACIES AND DENTAL ANOMALIES,,,,,,,C5543197,,602075;619228,MONDO:0030988,developmental delay with dysmorphic facies and dental anomalies,
+BMGC_DS18365,BMG_DS070552,,DEN HOED-DE BOER-VOISIN SYNDROME,,,,,,,C5543202,,602075;619229,MONDO:0030990,Kohlschutter-Tonz syndrome-like,
+BMGC_DS18366,BMG_DS070553,,BILE ACID CONJUGATION DEFECT 1,,,,,,,C5543203,,602938;619232,MONDO:0030991,bile acid conjugation defect 1,
+BMGC_DS18367,BMG_DS070554,,"SHORT STATURE, OLIGODONTIA, DYSMORPHIC FACIES, AND MOTOR DELAY",,,,,,,C5543206,,617457;619234,MONDO:0030992,"short stature, oligodontia, dysmorphic facies, and motor delay",
+BMGC_DS18368,BMG_DS070555,,IMMUNODEFICIENCY 79,,,,,DOID:0112277,immunodeficiency 79,C5543220,,186940;619238,MONDO:0030981,immunodeficiency 79,
+BMGC_DS18369,BMG_DS070556,,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES,,,,,,,C5543225,,619239,MONDO:0030994,neurodevelopmental disorder with or without autism or seizures,
+BMGC_DS18370,BMG_DS070557,,GLOBAL DEVELOPMENTAL DELAY WITH SPEECH AND BEHAVIORAL ABNORMALITIES,,,,,,,C5543226,,619243;610740,MONDO:0030995,global developmental delay with speech and behavioral abnormalities,
+BMGC_DS18371,BMG_DS070558,,NEURODEVELOPMENTAL DISORDER WITH CEREBRAL ATROPHY AND VARIABLE FACIAL DYSMORPHISM,,,,,,,C5543228,,619244;619014,MONDO:0030999,neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism,
+BMGC_DS18372,BMG_DS070559,,PREMATURE OVARIAN FAILURE 19,,,,,DOID:0112278,primary ovarian insufficiency 19,C5543229,,604554;619245,MONDO:0030985,premature ovarian failure 19,
+BMGC_DS18373,BMG_DS070560,,BARALLE-MACKEN SYNDROME,,,,,,,C5543241,,600959;619255,MONDO:0031002,Baralle-Macken syndrome,
+BMGC_DS18374,BMG_DS070561,,"HYPERCHOLANEMIA, FAMILIAL, 2",,,,,,,C5543243,,619256;182396,MONDO:0031003,"hypercholanemia, familial, 2",
+BMGC_DS18375,BMG_DS070562,,SPERMATOGENIC FAILURE 53,,,,,DOID:0112279,spermatogenic failure 53,C5543253,,619258;619251,MONDO:0030989,spermatogenic failure 53,
+BMGC_DS18376,BMG_DS070563,,NEURODEGENERATION WITH ATAXIA AND LATE-ONSET OPTIC ATROPHY,,,,,,,C5543254,,600857;619259,MONDO:0031006,neurodegeneration with ataxia and late-onset optic atrophy,
+BMGC_DS18377,BMG_DS070564,,"SPONDYLOEPIPHYSEAL DYSPLASIA, SENSORINEURAL HEARING LOSS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND LEBER CONGENITAL AMAUROSIS",,,,,DOID:0112290,"spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis",C5543257,,608700;619260,MONDO:0031007,"spondyloepiphyseal dysplasia, sensorineural hearing loss, impaired intellectual development, and leber congenital amaurosis",
+BMGC_DS18378,BMG_DS070565,,"NEPHROTIC SYNDROME, TYPE 24",,,,,,,C5543267,,619263;606627,MONDO:0031008,"nephrotic syndrome, type 24",
+BMGC_DS18379,BMG_DS070566,,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND VARIABLE SEIZURES,,,,,,,C5543268,,619264;614545,MONDO:0031011,neurodevelopmental disorder with dysmorphic facies and variable seizures,
+BMGC_DS18380,BMG_DS070567,,GLANZMANN THROMBASTHENIA 2,,,,,,,C5543273,,173470;619267,MONDO:0031009,Glanzmann thrombasthenia 2,
+BMGC_DS18381,BMG_DS070568,,ALZAHRANI-KUWAHARA SYNDROME,,,,,,,C5543274,,613175;619268,MONDO:0859136,Alzahrani-Kuwahara syndrome,
+BMGC_DS18382,BMG_DS070569,,ODONTOCHONDRODYSPLASIA 2 WITH HEARING LOSS AND DIABETES,,,,,,,C5543275,,619269,MONDO:0031010,odontochondrodysplasia 2 with hearing loss and diabetes,
+BMGC_DS18383,BMG_DS070570,,"BLEEDING DISORDER, PLATELET-TYPE, 24",,,,,,,C5543280,,619271;173470,MONDO:0030996,"bleeding disorder, platelet-type, 24",
+BMGC_DS18384,BMG_DS070571,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 37",,,,,,,C5543281,,619272;603359,MONDO:0030997,"mitochondrial complex 1 deficiency, nuclear type 37",
+BMGC_DS18385,BMG_DS070572,1332508004,CIMDAG syndrome,,,,,,,C5543287,,619273,MONDO:0035819,cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome,"CIMDAG syndrome | Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation syndrome (disorder) | Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation syndrome | Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anaemia, growth retardation syndrome | CIMDAG (cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation) syndrome | CIMDAG (cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anaemia, growth retardation) syndrome"
+BMGC_DS18386,BMG_DS070573,,"DEAFNESS, AUTOSOMAL DOMINANT 80",,,,,DOID:0070602,autosomal dominant nonsyndromic deafness 80,C5543289,,619274;617782,MONDO:0030998,"hearing loss, autosomal dominant 80",
+BMGC_DS18387,BMG_DS070574,,"MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME 2",,,,,,,C5543294,,619278;611483,MONDO:0025690,"microcephaly, epilepsy, and diabetes syndrome 2",
+BMGC_DS18388,BMG_DS070575,,PARKINSONISM WITH POLYNEUROPATHY,,,,,,,C5543299,,619279;191328,MONDO:0036193,parkinsonism with polyneuropathy,
+BMGC_DS18389,BMG_DS070576,,"IMMUNODEFICIENCY 14B, AUTOSOMAL RECESSIVE",,,,,,,C5543301,,602839;619281,MONDO:0023655,"immunodeficiency 14b, autosomal recessive",
+BMGC_DS18390,BMG_DS070577,,"NEURODEVELOPMENTAL DISORDER WITH SPASTICITY, CATARACTS, AND CEREBELLAR HYPOPLASIA",,,,,,,C5543306,,619286;605044,MONDO:0859137,"neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia",
+BMGC_DS18391,BMG_DS070578,,DYSTONIA 30,,,,,DOID:0060937,dystonia 30,C5543312,,619291;608550,MONDO:0025691,dystonia 30,
+BMGC_DS18392,BMG_DS070579,,KINSSHIP SYNDROME,,,,,DOID:0112383,KINSSHIP syndrome,C5543317,,601464;619297,MONDO:0851095,KINSSHIP syndrome,
+BMGC_DS18393,BMG_DS070580,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 14",,,,,DOID:0112325,pontocerebellar hypoplasia type 14,C5543322,,601301;619301,MONDO:0030258,"pontocerebellar hypoplasia, type 14",
+BMGC_DS18394,BMG_DS070581,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 15",,,,,DOID:0112326,pontocerebellar hypoplasia type 15,C5543326,,605585;619302,MONDO:0030259,"pontocerebellar hypoplasia, type 15",
+BMGC_DS18395,BMG_DS070582,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 1E",,,,,DOID:0112330,pontocerebellar hypoplasia type 1E,C5543328,,619303;610826,MONDO:0030260,"pontocerebellar hypoplasia, type 1E",
+BMGC_DS18396,BMG_DS070583,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 1F",,,,,DOID:0112331,pontocerebellar hypoplasia type 1F,C5543331,,619304;606493,MONDO:0030261,"pontocerebellar hypoplasia, type 1F",
+BMGC_DS18397,BMG_DS070584,,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND CEREBELLAR HYPOPLASIA,,,,,,,C5543332,,615329;619306,MONDO:0859141,neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia,
+BMGC_DS18398,BMG_DS070585,,"LEUKODYSTROPHY, HYPOMYELINATING, 21",,,,,DOID:0070407,hypomyelinating leukodystrophy 21,C5543334,,619310,MONDO:0030263,"leukodystrophy, hypomyelinating, 21",
+BMGC_DS18399,BMG_DS070586,,HIATT-NEU-COOPER NEURODEVELOPMENTAL SYNDROME,,,,,,,C5543338,,179550;619311,MONDO:0859142,Hiatt-Neu-Cooper neurodevelopmental syndrome,
+BMGC_DS18400,BMG_DS070587,,RADIO-TARTAGLIA SYNDROME,,,,,,,C5543339,,613484;619312,MONDO:0859143,Radio-Tartaglia syndrome,
+BMGC_DS18401,BMG_DS070588,,IMMUNODEFICIENCY 80 WITH OR WITHOUT CONGENITAL CARDIOMYOPATHY,,,,,,,C5543344,,619313,MONDO:0030266,immunodeficiency 80 with or without congenital cardiomyopathy,
+BMGC_DS18402,BMG_DS070589,,BURATTI-HAREL SYNDROME,,,,,,,C5543351,,602212;619314,MONDO:0859144,Buratti-Harel syndrome,
+BMGC_DS18403,BMG_DS070590,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 6B,,,,,DOID:0070379,developmental and epileptic encephalopathy 6B,C5543353,,182389;619317,MONDO:0030268,developmental and epileptic encephalopathy 6B,
+BMGC_DS18404,BMG_DS070591,,OCULOGASTROINTESTINAL NEURODEVELOPMENTAL SYNDROME,,,,,,,C5543355,,619318;603267,MONDO:0036189,oculogastrointestinal-neurodevelopmental syndrome,
+BMGC_DS18405,BMG_DS070592,,LYMPHATIC MALFORMATION 9,,,,,,,C5543365,,619319;604523,MONDO:0030270,lymphatic malformation 9,
+BMGC_DS18406,BMG_DS070593,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 65",,,,,,,C5543371,,609765;619320,MONDO:0023657,"intellectual developmental disorder, autosomal dominant 65",
+BMGC_DS18407,BMG_DS070594,,"GROWTH RESTRICTION, HYPOPLASTIC KIDNEYS, ALOPECIA, AND DISTINCTIVE FACIES",,,,,,,C5543375,,603901;619321,MONDO:0859146,"growth restriction, hypoplastic kidneys, alopecia, and distinctive facies",
+BMGC_DS18408,BMG_DS070595,,MARBACH-RUSTAD PROGEROID SYNDROME,,,,,,,C5543388,,616312;619322,MONDO:0859147,Marbach-Rustad progeroid syndrome,
+BMGC_DS18409,BMG_DS070596,,NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND GINGIVAL OVERGROWTH,,,,,,,C5543395,,619323;619152,MONDO:0859148,neurodevelopmental disorder with seizures and gingival overgrowth,
+BMGC_DS18410,BMG_DS070597,,HYPERTRIGLYCERIDEMIA 2,,,,,,,C5543398,,611998;619324,MONDO:0859149,hypertriglyceridemia 2,
+BMGC_DS18411,BMG_DS070598,1340175001,CPE-related Prader-Willi-like syndrome,,,,,,,C5543403,,619326,MONDO:0859150,BDV syndrome,Blakemore Durmaz Vasileiou syndrome | BDV (Blakemore Durmaz Vasileiou) syndrome | Carboxypeptidase E-related Prader-Willi-like syndrome | CPE-related Prader-Willi-like syndrome | Carboxypeptidase E-related Prader-Willi-like syndrome (disorder) | BDV syndrome
+BMGC_DS18412,BMG_DS070599,,"LEUKODYSTROPHY, HYPOMYELINATING, 22",,,,,DOID:0070402,hypomyelinating leukodystrophy 22,C5543406,,601326;619328,MONDO:0025701,"leukodystrophy, hypomyelinating, 22",
+BMGC_DS18413,BMG_DS070600,,"FIBROMUSCULAR DYSPLASIA, MULTIFOCAL",,,,,,,C5543412,,120215;619329,MONDO:0859151,"fibromuscular dysplasia, multifocal",
+BMGC_DS18414,BMG_DS070601,,NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND MOTOR DYSFUNCTION,,,,,DOID:0070443,neurodevelopmental disorder with cerebellar atrophy and motor dysfunction,C5543427,,619333;607005,MONDO:0859152,neurodevelopmental disorder with cerebellar atrophy and motor dysfunction,
+BMGC_DS18415,BMG_DS070602,,ARTHROGRYPOSIS MULTIPLEX CONGENITA 6,,,,,DOID:0070336,arthrogryposis multiplex congenita-6,C5543431,,619334;161650,MONDO:0030281,arthrogryposis multiplex congenita 6,
+BMGC_DS18416,BMG_DS070603,,"CATARACTS, SPASTIC PARAPARESIS, AND SPEECH DELAY",,,,,,,C5543440,,619338,,,
+BMGC_DS18417,BMG_DS070604,,BARTSOCAS-PAPAS SYNDROME 2,,,,,,,C5543445,,619339,MONDO:0859154,Bartsocas-Papas syndrome 2,
+BMGC_DS18418,BMG_DS070605,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 96,,,,,DOID:0070377,developmental and epileptic encephalopathy 96,C5543446,,619340;601633,MONDO:0023659,developmental and epileptic encephalopathy 96,
+BMGC_DS18419,BMG_DS070606,,VISCERAL MYOPATHY 2,,,,,,,C5543466,,619350;160745,MONDO:0859157,visceral myopathy 2,
+BMGC_DS18420,BMG_DS070607,,MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 2,,,,,,,C5543476,,619351;160745,MONDO:0025708,megacystis-microcolon-intestinal hypoperistalsis syndrome 2,
+BMGC_DS18421,BMG_DS070608,,"ATAXIA, INTENTION TREMOR, AND HYPOTONIA SYNDROME, CHILDHOOD-ONSET",,,,,,,C5543478,,619352;601632,MONDO:0859158,"ataxia, intention tremor, and hypotonia syndrome, childhood-onset",
+BMGC_DS18422,BMG_DS070609,,"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY",,,,,,,C5543482,,619354;186852,MONDO:0859159,"deafness, cataract, impaired intellectual development, and polyneuropathy",
+BMGC_DS18423,BMG_DS070610,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 22",,,,,DOID:0070507,mitochondrial complex IV deficiency nuclear type 22,C5543491,,618064;619355,MONDO:0859160,"mitochondrial complex IV deficiency, nuclear type 22",
+BMGC_DS18424,BMG_DS070611,,"ONYCHODYSTROPHY, OSTEODYSTROPHY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES SYNDROME",,,,,,,C5543496,,600153;619356,MONDO:0859161,"onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome",
+BMGC_DS18425,BMG_DS070612,,"ANGIOEDEMA, HEREDITARY, 4",,,,,,,C5543503,,173350;619360,MONDO:0025712,"angioedema, hereditary, 4",
+BMGC_DS18426,BMG_DS070613,,"ANGIOEDEMA, HEREDITARY, 5",,,,,,,C5543508,,619361;601667,MONDO:0030293,"angioedema, hereditary, 5",
+BMGC_DS18427,BMG_DS070614,,MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 3,,,,,,,C5543513,,602715;619362,MONDO:0030294,megacystis-microcolon-intestinal hypoperistalsis syndrome 3,
+BMGC_DS18428,BMG_DS070615,,"ANGIOEDEMA, HEREDITARY, 6",,,,,,,C5543516,,612358;619363,MONDO:0023660,"angioedema, hereditary, 6",
+BMGC_DS18429,BMG_DS070616,,MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 4,,,,,,,C5543519,,609905;619365,MONDO:0030296,megacystis-microcolon-intestinal hypoperistalsis syndrome 4,
+BMGC_DS18430,BMG_DS070617,,"ANGIOEDEMA, HEREDITARY, 7",,,,,,,C5543526,,604603;619366,MONDO:0025713,"angioedema, hereditary, 7",
+BMGC_DS18431,BMG_DS070618,,"ANGIOEDEMA, HEREDITARY, 8",,,,,,,C5543528,,619210;619367,MONDO:0030298,"angioedema, hereditary, 8",
+BMGC_DS18432,BMG_DS070619,,LYMPHATIC MALFORMATION 10,,,,,,,C5543531,,601922;619369,MONDO:0023662,lymphatic malformation 10,
+BMGC_DS18433,BMG_DS070620,,"CARDIOMYOPATHY, DILATED, 2D",,,,,DOID:0081160,dilated cardiomyopathy 2D,C5543535,,617416;619371,MONDO:0030300,"cardiomyopathy, dilated, 2D",
+BMGC_DS18434,BMG_DS070621,,NEURODEVELOPMENTAL DISORDER WITH INFANTILE EPILEPTIC SPASMS,,,,,,,C5543538,,619373;608458,MONDO:0859162,neurodevelopmental disorder with infantile epileptic spasms,
+BMGC_DS18435,BMG_DS070622,,IMMUNODEFICIENCY 81,,,,,,,C5543540,,619374;601603,MONDO:0030302,immunodeficiency 81,
+BMGC_DS18436,BMG_DS070623,,"AUTOINFLAMMATORY SYNDROME, FAMILIAL, WITH OR WITHOUT IMMUNODEFICIENCY",,,,,,,C5543547,,603597;619375,MONDO:0800130,autoinflammatory syndrome with immunodeficiency,
+BMGC_DS18437,BMG_DS070624,,FAUNDES-BANKA SYNDROME,,,,,,,C5543554,,600187;619376,MONDO:0859163,Faundes-Banka syndrome,
+BMGC_DS18438,BMG_DS070625,,OSTEOOTOHEPATOENTERIC SYNDROME,,,,,,,C5543557,,611219;619377,MONDO:0859164,osteootohepatoenteric syndrome,
+BMGC_DS18439,BMG_DS070626,,SPERMATOGENIC FAILURE 54,,,,,DOID:0112335,spermatogenic failure 54,C5543570,,619387;619379,MONDO:0023664,spermatogenic failure 54,
+BMGC_DS18440,BMG_DS070627,,SPERMATOGENIC FAILURE 55,,,,,DOID:0112337,spermatogenic failure 55,C5543580,,619380;616554,MONDO:0030307,spermatogenic failure 55,
+BMGC_DS18441,BMG_DS070628,,IMMUNODEFICIENCY 82 WITH SYSTEMIC INFLAMMATION,,,,,,,C5543581,,600085;619381,MONDO:0030308,immunodeficiency 82 with systemic inflammation,
+BMGC_DS18442,BMG_DS070629,,"LEBER-LIKE HEREDITARY OPTIC NEUROPATHY, AUTOSOMAL RECESSIVE 1",,,,,,,C5543589,,618202;619382,MONDO:0030309,"Leber hereditary optic neuropathy, autosomal recessive",
+BMGC_DS18443,BMG_DS070630,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES",,,,,,,C5543591,,618159;619383,MONDO:0859165,"neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities",
+BMGC_DS18444,BMG_DS070631,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 52,,,,,DOID:0070425,combined oxidative phosphorylation deficiency 52,C5543592,,603485;619386,MONDO:0030311,combined oxidative phosphorylation deficiency 52,
+BMGC_DS18445,BMG_DS070632,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 29",,,,,DOID:0070410,autosomal recessive spinocerebellar ataxia 29,C5543595,,619389;605485,MONDO:0030312,"spinocerebellar ataxia, autosomal recessive 29",
+BMGC_DS18446,BMG_DS070633,,,,,,,,,C5543600,,619396,MONDO:0030313,"encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 10",
+BMGC_DS18447,BMG_DS070634,,LYMPHATIC MALFORMATION 11,,,,,,,C5543614,,619401;600222,MONDO:0030316,lymphatic malformation 11,
+BMGC_DS18448,BMG_DS070635,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 28",,,,,,,C5543616,,619402;609691,MONDO:0030317,"cardiomyopathy, familial hypertrophic, 28",
+BMGC_DS18449,BMG_DS070636,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 30",,,,,DOID:0070411,autosomal recessive spinocerebellar ataxia 30,C5543620,,619405;618211,MONDO:0030318,"spinocerebellar ataxia, autosomal recessive 30",
+BMGC_DS18450,BMG_DS070637,,HYPOKALEMIC TUBULOPATHY AND DEAFNESS,,,,,,,C5543621,,605722;619406,MONDO:0859167,hypokalemic tubulopathy and deafness,
+BMGC_DS18451,BMG_DS070638,,WHIM SYNDROME 2,,,,,DOID:0060973,WHIM syndrome 2,C5543622,,619407;146928,MONDO:0030374,WHIM syndrome 2,
+BMGC_DS18452,BMG_DS070639,,"NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET 2",,,,,,,C5543623,,603623;619418,MONDO:0030375,"neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2",
+BMGC_DS18453,BMG_DS070640,,MARTSOLF SYNDROME 2,,,,,,,C5543626,,602536;619420,MONDO:0030376,Martsolf syndrome 2,
+BMGC_DS18454,BMG_DS070641,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 31",,,,,DOID:0070412,autosomal recessive spinocerebellar ataxia 31,C5543627,,619422;608760,MONDO:0030323,"spinocerebellar ataxia, autosomal recessive 31",
+BMGC_DS18455,BMG_DS070642,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 53,,,,,DOID:0070426,combined oxidative phosphorylation deficiency 53,C5543631,,619423;619219,MONDO:0030378,combined oxidative phosphorylation deficiency 53,
+BMGC_DS18456,BMG_DS070643,,MITOCHONDRIAL DNA DEPLETION SYNDROME 16B (NEUROOPHTHALMIC TYPE),,,,,DOID:0070447,mitochondrial DNA depletion syndrome 16B,C5543632,,604983;619425,MONDO:0030326,mitochondrial dna depletion syndrome 16B (neuroophthalmic type),
+BMGC_DS18457,BMG_DS070644,,WHITE-KERNOHAN SYNDROME,,,,,,,C5543635,,600045;619426,MONDO:0859169,White-Kernohan syndrome,
+BMGC_DS18458,BMG_DS070645,,MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 5,,,,,,,C5543636,,619431;102545,MONDO:0030329,megacystis-microcolon-intestinal hypoperistalsis syndrome 5,
+BMGC_DS18459,BMG_DS070646,,"CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 6",,,,,,,C5543638,,619433;605664,MONDO:0030330,"cardiomyopathy, familial restrictive, 6",
+BMGC_DS18460,BMG_DS070647,,"CILIARY DYSKINESIA, PRIMARY, 46",,,,,,,C5543646,,619436;607652,MONDO:0030332,"ciliary dyskinesia, primary, 46",
+BMGC_DS18461,BMG_DS070648,,"HYPERTRIIODOTHYRONINEMIA, FAMILIAL DYSALBUMINEMIC",,,,,,,C5543652,,615999;103600,,,
+BMGC_DS18462,BMG_DS070678,,Neuroinflammatory Diseases,Neuroinflammatory Diseases,,,,,,C5544451,D000090862,,,,
+BMGC_DS18463,BMG_DS070680,,Dominantly-Inherited Spinocerebellar Ataxias,Spinocerebellar Ataxias,,,,,,C5544494,D020754,,,,
+BMGC_DS18464,BMG_DS070692,,Chronic Condition,Chronic Disease,,,,,,C5545294,D002908,,,,
+BMGC_DS18465,BMG_DS070790,1144934003,Recurrent infection due to specific granule deficiency,,,,,,,C5546032,,,,,Recurrent infection due to specific granule deficiency | Recurrent infection due to specific granule deficiency (disorder)
+BMGC_DS18466,BMG_DS070883,,,,,,,,,C5546764,,,MONDO:0017243,bullous diffuse cutaneous mastocytosis,
+BMGC_DS18467,BMG_DS071119,1156763004,Progressive supranuclear palsy corticobasal syndrome,,,,,,,C5548189,,,MONDO:0016563,progressive supranuclear palsy-corticobasal syndrome,Progressive supranuclear palsy corticobasal syndrome (disorder) | Progressive supranuclear palsy corticobasal syndrome
+BMGC_DS18468,BMG_DS071124,1156791007,Atypical glycine encephalopathy,,,,,,,C5548198,,,,,Atypical glycine encephalopathy | Atypical glycine encephalopathy (disorder) | Atypical non-ketotic hyperglycinemia | Atypical non-ketotic hyperglycinaemia
+BMGC_DS18469,BMG_DS071125,1156803005,Neonatal glycine encephalopathy,,,,,,,C5548200,,,MONDO:0017353,neonatal glycine encephalopathy,Neonatal glycine encephalopathy (disorder) | Neonatal glycine encephalopathy | Neonatal non-ketotic hyperglycinemia | Neonatal non-ketotic hyperglycinaemia
+BMGC_DS18470,BMG_DS071126,,,,,,,,,C5548205,,,MONDO:0016860,familial adenomatous polyposis due to 5q22.2 microdeletion,
+BMGC_DS18471,BMG_DS071130,1156826003,Infantile glycine encephalopathy,,,,,,,C5548209,,,MONDO:0017354,infantile glycine encephalopathy,Infantile glycine encephalopathy (disorder) | Infantile glycine encephalopathy | Infantile non-ketotic hyperglycinaemia | Infantile non-ketotic hyperglycinemia
+BMGC_DS18472,BMG_DS071133,1156837002,Autosomal dominant distal hereditary motor neuropathy,,,,,,,C5548212,,,MONDO:0015362,"neuronopathy, distal hereditary motor, autosomal dominant",Autosomal dominant distal hereditary motor neuropathy (disorder) | Autosomal dominant distal hereditary motor neuropathy
+BMGC_DS18473,BMG_DS071134,1156838007,X-linked thrombocytopenia with normal platelets,,,,,,,C5548213,,,,,X-linked thrombocytopenia with normal platelets (disorder) | X-linked thrombocytopenia with normal platelets | X-linked thrombocytopaenia with normal platelets
+BMGC_DS18474,BMG_DS071188,1156850001,Autosomal recessive distal hereditary motor neuropathy,,,,,,,C5548369,,,MONDO:0015363,"neuronopathy, distal hereditary motor, autosomal recessive",Autosomal recessive distal hereditary motor neuropathy (disorder) | Autosomal recessive distal hereditary motor neuropathy
+BMGC_DS18475,BMG_DS071189,1156764005,Progressive supranuclear palsy parkinsonism syndrome,,,,,,,C5548370,,,,,Progressive supranuclear palsy parkinsonism syndrome (disorder) | Progressive supranuclear palsy parkinsonism syndrome
+BMGC_DS18476,BMG_DS071202,28259009;8933000,Crigler-Najjar syndrome,,5C58.00,CriglerNajjar syndrome,E80.5,,,C5551003,,,MONDO:0009044,Crigler-Najjar syndrome,"Crigler-Najjar syndrome | Crigler-Najjar syndrome (disorder) | Crigler-Najjar syndrome, type I | Deficiency of glucuronosyltransferase | Glucuronyltransferase deficiency | UDP glucuronyl transferase deficiency | Crigler-Najjar type 1 | Bilirubin UDP glucuronyl transferase deficiency | Bilirubin glucuronosyltransferase deficiency | Crigler-Najjar syndrome type I | Crigler-Najjar syndrome, type I (disorder)"
+BMGC_DS18477,BMG_DS071204,,"HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2",,,,,DOID:0080958,primary hypoalphalipoproteinemia 2,C5551172,,107680;618463,MONDO:0032766,"hypoalphalipoproteinemia, primary, 2",
+BMGC_DS18478,BMG_DS071209,3752003;154413002,Trichuriasis,,,,B79,,,C5551334,,,MONDO:0005996,trichuriasis,Trichuriasis | Trichocephaliasis | Whipworm infection | Trichuriosis | Trichuriasis - whipworm | Trichuriasis (disorder) | Infection by Trichuris | Trichuriasis | Trichuriasis (disorder)
+BMGC_DS18479,BMG_DS071210,,"DYSKINESIA WITH OROFACIAL INVOLVEMENT, AUTOSOMAL DOMINANT",,,,,,,C5551343,,606703;600293,MONDO:0800028,"dyskinesia with orofacial involvement, autosomal dominant",
+BMGC_DS18480,BMG_DS071211,,AICARDI-GOUTIERES SYNDROME 8,,,,,,,C5551352,,619486;617910,MONDO:0030361,Aicardi-Goutieres syndrome 8,
+BMGC_DS18481,BMG_DS071212,19824006,Infection of skin and/or subcutaneous tissue,,,,,,,C5551358,,,,,Infective dermatological disorders | Skin infection | Skin and subcutaneous tissue infection | Infection of skin and/or subcutaneous tissue (disorder) | Infection of skin and/or subcutaneous tissue
+BMGC_DS18482,BMG_DS071214,,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND THIN CORPUS CALLOSUM,,,,,DOID:0070469,neurodevelopmental disorder with dysmorphic facies and thin corpus callosum,C5551361,,605012;619480,MONDO:0859179,neurodevelopmental disorder with dysmorphic facies and thin corpus callosum,
+BMGC_DS18483,BMG_DS071215,,NEUROOCULAR SYNDROME 1,,,,,,,C5551362,,616633;619539,MONDO:0859193,neuroocular syndrome,
+BMGC_DS18484,BMG_DS071217,,"CEROID LIPOFUSCINOSIS, NEURONAL, 6A",,,,,,,C5551375,,601780;606725,MONDO:0011144,"ceroid lipofuscinosis, neuronal, 6A",
+BMGC_DS18485,BMG_DS071220,,"Muscular Dystrophy, Distal, Late-Onset, Autosomal Recessive",,,,,DOID:0070198,Miyoshi muscular dystrophy,C5551399,C537480,,,,
+BMGC_DS18486,BMG_DS071221,432241000124101;1173024006,Typical absence seizure,,,,,,,C5551411,,,,,Typical absence seizure (disorder) | Typical absence seizure | Typical absence seizure | Typical absence seizure (finding)
+BMGC_DS18487,BMG_DS071223,,,,,,,,,C5551428,,,MONDO:0003669,testicular seminoma,
+BMGC_DS18488,BMG_DS071224,,,,,,,,,C5551440,,122750,MONDO:0007391,coxa vara,
+BMGC_DS18489,BMG_DS071227,,"OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE",,,,,DOID:0080026,"otospondylomegaepiphyseal dysplasia, autosomal recessive",C5551484,,215150;120290,MONDO:0044206,"otospondylomegaepiphyseal dysplasia, autosomal recessive",
+BMGC_DS18490,BMG_DS071229,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 21",,,,,DOID:0112022,non-syndromic X-linked intellectual disability 21,C5551510,,300206;300143,MONDO:0010256,"intellectual disability, X-linked 21",
+BMGC_DS18491,BMG_DS071232,7297005,Generalized seborrheic dermatitis of infants,,,,,,,C5551904,,,MONDO:0017787,erythroderma desquamativum,Generalized seborrheic dermatitis of infants | Leiner's disease | Erythroderma desquamativum | Infantile seborrheic dermatitis | Infantile seborrhoeic dermatitis | Generalised seborrhoeic dermatitis of infants | Generalized seborrheic dermatitis of infants (disorder)
+BMGC_DS18492,BMG_DS071233,,,,,,,,,C5552731,,,MONDO:0019123,continuous spikes and waves during sleep,
+BMGC_DS18493,BMG_DS071234,,,,,,,,,C5552985,,133180,MONDO:0007573,"erythroleukemia, familial, susceptibility to",
+BMGC_DS18494,BMG_DS071235,,Miyoshi myopathy,,,,,DOID:0070198,Miyoshi muscular dystrophy,C5553104,C537480,,MONDO:0009685,Miyoshi myopathy,
+BMGC_DS18495,BMG_DS071240,,,,,,,,,C5554190,,,MONDO:0018761,SMARCA4-deficient sarcoma of thorax,
+BMGC_DS18496,BMG_DS071241,,,,,,,,,C5554234,,,MONDO:0016418,"multiple system atrophy, cerebellar type",
+BMGC_DS18497,BMG_DS071242,,,,,,,,,C5554235,,,MONDO:0020352,"multiple system atrophy, parkinsonian type",
+BMGC_DS18498,BMG_DS071257,,,,,,,,,C5555857,,,MONDO:0021060,RASopathy,
+BMGC_DS18499,BMG_DS071258,1177176009,Intermediate epidermolysis bullosa simplex with cardiomyopathy,,,,,,,C5555869,,,,,Intermediate epidermolysis bullosa simplex with cardiomyopathy (disorder) | Intermediate epidermolysis bullosa simplex with cardiomyopathy
+BMGC_DS18500,BMG_DS071260,,,,,,,DOID:3700,uterine ligament adenocarcinoma,C5557428,,,,,
+BMGC_DS18501,BMG_DS071261,,,,,,,DOID:3699,uterine ligament mucinous adenocarcinoma,C5557429,,,,,
+BMGC_DS18502,BMG_DS071262,,,,,,,DOID:5829,uterine ligament endometrioid adenocarcinoma,C5557430,,,,,
+BMGC_DS18503,BMG_DS071263,,,,,,,DOID:5302,uterine ligament clear cell adenocarcinoma,C5557431,,,,,
+BMGC_DS18504,BMG_DS071264,,,,,,,DOID:8178,endometrial type cervical adenomyoma,C5557432,,,,,
+BMGC_DS18505,BMG_DS071275,,"EPIDERMOLYSIS BULLOSA SIMPLEX 1B, GENERALIZED INTERMEDIATE",,,,,DOID:0080511,epidermolysis bullosa simplex generalized type,C5561924,,131900;148066,MONDO:0007554,"epidermolysis bullosa simplex 1B, generalized intermediate",
+BMGC_DS18506,BMG_DS071276,,RETINITIS PIGMENTOSA 91,,,,,,,C5561925,,153870;602870,MONDO:0007934,benign concentric annular macular dystrophy,
+BMGC_DS18507,BMG_DS071277,,INTERSTITIAL LUNG DISEASE 2,,,,,DOID:0060971,interstitial lung disease 2,C5561926,,178500;178642,MONDO:0800029,interstitial lung disease 2,
+BMGC_DS18508,BMG_DS071278,,"CEROID LIPOFUSCINOSIS, NEURONAL, 6B (KUFS TYPE)",,,,,,,C5561927,,606725;204300,MONDO:0008768,"ceroid lipofuscinosis, neuronal, 6B (Kufs type)",
+BMGC_DS18509,BMG_DS071279,,,,,,,,,C5561928,,206500,MONDO:0008791,anencephaly 1,
+BMGC_DS18510,BMG_DS071280,,"LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS 1",,,,,DOID:0080523,adult-onset leukoencephalopathy with axonal spheroids and pigmented glia,C5561929,,221820,MONDO:0800027,"leukoencephalopathy, diffuse hereditary, with spheroids 1",
+BMGC_DS18511,BMG_DS071281,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, WITH PIGMENTARY MOSAICISM AND COARSE FACIES",,,,,,,C5561930,,301066;314310,MONDO:0859080,"intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies",
+BMGC_DS18512,BMG_DS071282,,,,,,,,,C5561931,,602477,MONDO:0100519,"epilepsy, idiopathic generalized, susceptibility to, 17",
+BMGC_DS18513,BMG_DS071283,,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 11",,,,,DOID:0111310,familial febrile seizures 2,C5561932,,602477;602781,,,
+BMGC_DS18514,BMG_DS071284,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2GG",,,,,,,C5561933,,603698;606483,MONDO:0011675,"Charcot-Marie-Tooth Disease, axonal, type 2GG",
+BMGC_DS18515,BMG_DS071285,,"BILE ACID MALABSORPTION, PRIMARY, 1",,,,,,,C5561934,,613291;601295,MONDO:0013214,"bile acid malabsorption, primary, 1",
+BMGC_DS18516,BMG_DS071286,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw, AUTOSOMAL RECESSIVE",,,,,DOID:0080572,congenital disorder of glycosylation Iw,C5561935,,615596;601134,MONDO:0014270,STT3A-congenital disorder of glycosylation,
+BMGC_DS18517,BMG_DS071287,,BARDET-BIEDL SYNDROME 22,,,,,DOID:0081011,Bardet-Biedl syndrome 22,C5561936,,608040;617119,MONDO:0014926,Bardet-Biedl syndrome 22,
+BMGC_DS18518,BMG_DS071288,,"MYOPATHY, MYOFIBRILLAR, 12, INFANTILE-ONSET, WITH CARDIOMYOPATHY",,,,,,,C5561937,,160781;619424,MONDO:0859168,"myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy",
+BMGC_DS18519,BMG_DS071289,,FOCAL SEGMENTAL GLOMERULOSCLEROSIS AND NEURODEVELOPMENTAL SYNDROME,,,,,,,C5561938,,606125;619428,MONDO:0100111,focal segmental glomerulosclerosis and neurodevelopmental syndrome,
+BMGC_DS18520,BMG_DS071290,,RITSCHER-SCHINZEL SYNDROME 4,,,,,,,C5561939,,608383;619435,MONDO:0030331,Ritscher-Schinzel syndrome 4,
+BMGC_DS18521,BMG_DS071291,,IMMUNODEFICIENCY 84,,,,,,,C5561940,,606221;619437,MONDO:0030333,immunodeficiency 84,
+BMGC_DS18522,BMG_DS071292,,,,,,,,,C5561941,,619441,MONDO:0030334,"encephalitis, acute, infection (viral)-induced, susceptibility to, 11",
+BMGC_DS18523,BMG_DS071293,,"DIARRHEA 12, WITH MICROVILLUS ATROPHY",,,,,,,C5561942,,600876;619445,MONDO:0030335,"diarrhea 12, with microvillus atrophy",
+BMGC_DS18524,BMG_DS071294,,RETINAL DYSTROPHY AND MICROVILLUS INCLUSION DISEASE,,,,,,,C5561943,,619446;600876,MONDO:0859170,retinal dystrophy and microvillus inclusion disease,
+BMGC_DS18525,BMG_DS071295,,"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIE",,,,,,,C5561944,,619451;150390,MONDO:0030337,"cutis laxa, autosomal recessive, type 2E",
+BMGC_DS18526,BMG_DS071296,,,,,,,,,C5561945,,619452,MONDO:0030338,anencephaly 2,
+BMGC_DS18527,BMG_DS071297,,LUO-SCHOCH-YAMAMOTO SYNDROME,,,,,DOID:0070416,Luo-Schoch-Yamamoto syndrome,C5561946,,619460;608985,MONDO:0859171,Luo-Schoch-Yamamoto syndrome,
+BMGC_DS18528,BMG_DS071298,,"MYASTHENIC SYNDROME, CONGENITAL, 7B, PRESYNAPTIC, AUTOSOMAL RECESSIVE",,,,,,,C5561947,,600104;619461,MONDO:0030341,"myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive",
+BMGC_DS18529,BMG_DS071299,,"PORTAL HYPERTENSION, NONCIRRHOTIC, 2",,,,,,,C5561948,,608086;619463,MONDO:0030397,"portal hypertension, noncirrhotic, 2",
+BMGC_DS18530,BMG_DS071300,,SICK SINUS SYNDROME 4,,,,,,,C5561949,,139390;619464,MONDO:0859173,sick sinus syndrome 4,
+BMGC_DS18531,BMG_DS071301,,"VISCERAL NEUROPATHY, FAMILIAL, 2, AUTOSOMAL RECESSIVE",,,,,,,C5561950,,164870;619465,MONDO:0030399,"visceral neuropathy, familial, 2, autosomal recessive",
+BMGC_DS18532,BMG_DS071302,,"CILIARY DYSKINESIA, PRIMARY, 47, AND LISSENCEPHALY",,,,,,,C5561951,,601990;619466,MONDO:0030346,"ciliary dyskinesia, primary, 47, and lissencephaly",
+BMGC_DS18533,BMG_DS071303,,"USMANI-RIAZUDDIN SYNDROME, AUTOSOMAL DOMINANT",,,,,,,C5561952,,619467;603533,MONDO:0859174,"Usmani-Riazuddin syndrome, autosomal dominant",
+BMGC_DS18534,BMG_DS071304,,NEPHRONOPHTHISIS-LIKE NEPHROPATHY 2,,,,,,,C5561953,,619468;610801,MONDO:0859175,nephronophthisis-like nephropathy 2,
+BMGC_DS18535,BMG_DS071305,,NEURODEVELOPMENTAL DISORDER WITH MOTOR AND SPEECH DELAY AND BEHAVIORAL ABNORMALITIES,,,,,,,C5561954,,619469;619470,MONDO:0859176,neurodevelopmental disorder with motor and speech delay and behavioral abnormalities,
+BMGC_DS18536,BMG_DS071306,,VISS SYNDROME,,,,,,,C5561955,,619472;605600,MONDO:0859177,VISS syndrome,
+BMGC_DS18537,BMG_DS071307,,OCULOPHARYNGODISTAL MYOPATHY 3,,,,,DOID:0081299,oculopharyngodistal myopathy 3,C5561956,,619473;618025,MONDO:0023671,oculopharyngodistal myopathy 3,
+BMGC_DS18538,BMG_DS071308,,,,,,,,,C5561957,,619475,MONDO:0859178,"developmental delay, impaired speech, and behavioral abnormalities",
+BMGC_DS18539,BMG_DS071309,,JOUBERT SYNDROME 38,,,,,,,C5561958,,619476;617112,MONDO:0030353,Joubert syndrome 38,
+BMGC_DS18540,BMG_DS071310,,"FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 3, DIGENIC",,,,,DOID:0060917,facioscapulohumeral muscular dystrophy 3,C5561959,,619477;615354,MONDO:0030354,"facioscapulohumeral muscular dystrophy 3, digenic",
+BMGC_DS18541,BMG_DS071311,,"FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 4, DIGENIC",,,,,DOID:0060918,facioscapulohumeral muscular dystrophy 4,C5561960,,619478;602900,MONDO:0030355,"facioscapulohumeral muscular dystrophy 4, digenic",
+BMGC_DS18542,BMG_DS071312,,SHORT-RIB THORACIC DYSPLASIA 21 WITHOUT POLYDACTYLY,,,,,,,C5561961,,619479,MONDO:0030356,short-rib thoracic dysplasia 21 without polydactyly,
+BMGC_DS18543,BMG_DS071313,,"BILE ACID MALABSORPTION, PRIMARY, 2",,,,,,,C5561962,,612085;619481,MONDO:0859180,"bile acid malabsorption, primary, 2",
+BMGC_DS18544,BMG_DS071314,,"CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 2, AND AUTONOMIC DYSFUNCTION",,,,,,,C5561963,,614636;619482,MONDO:0030537,"central hypoventilation syndrome, congenital, 2, and autonomic dysfunction",
+BMGC_DS18545,BMG_DS071315,,"CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 3",,,,,,,C5561964,,604255;619483,MONDO:0030539,"central hypoventilation syndrome, congenital, 3",
+BMGC_DS18546,BMG_DS071316,,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 6",,,,,,,C5561965,,612084;619484,MONDO:0030360,"cholestasis, progressive familial intrahepatic, 6",
+BMGC_DS18547,BMG_DS071317,,AICARDI-GOUTIERES SYNDROME 9,,,,,,,C5561966,,617876;619487,MONDO:0030362,Aicardi-Goutieres syndrome 9,
+BMGC_DS18548,BMG_DS071318,,DEGCAGS SYNDROME,,,,,,,C5561967,,609571;619488,MONDO:0859181,DEGCAGS syndrome,
+BMGC_DS18549,BMG_DS071319,,"SHORT STATURE, DAUBER-ARGENTE TYPE",,,,,,,C5561968,,619485;619489,MONDO:0859182,"Short stature, Dauber-Argente type",
+BMGC_DS18550,BMG_DS071320,,,,,,,,,C5561969,,619491,MONDO:0859183,"Parkinson disease 24, autosomal dominant, susceptibility to",
+BMGC_DS18551,BMG_DS071321,,"CARDIOMYOPATHY, DILATED, 2E",,,,,DOID:0081161,dilated cardiomyopathy 2E,C5561970,,605267;619492,MONDO:0030366,"cardiomyopathy, dilated, 2E",
+BMGC_DS18552,BMG_DS071322,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 2v",,,,,,,C5561971,,619493;610214,MONDO:0030423,"congenital disorder of glycosylation, type 2v",
+BMGC_DS18553,BMG_DS071323,,"DEAFNESS, AUTOSOMAL DOMINANT 81",,,,,DOID:0070608,autosomal dominant nonsyndromic deafness 81,C5561972,,615427;619500,MONDO:0030549,"hearing loss, autosomal dominant 81",
+BMGC_DS18554,BMG_DS071324,,VENTRICULOMEGALY AND ARTHROGRYPOSIS,,,,,,,C5561973,,619501;615759,MONDO:0859184,ventriculomegaly and arthrogryposis,
+BMGC_DS18555,BMG_DS071325,,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND DYSMORPHIC FACIES,,,,,,,C5561974,,619503;139390,MONDO:0859185,neurodevelopmental disorder with hypotonia and dysmorphic facies,
+BMGC_DS18556,BMG_DS071326,,CHOPRA-AMIEL-GORDON SYNDROME,,,,,,,C5561975,,615929;619504,MONDO:0859186,Chopra-Amiel-Gordon syndrome,
+BMGC_DS18557,BMG_DS071327,,IMMUNODEFICIENCY 85 AND AUTOIMMUNITY,,,,,,,C5561976,,604700;619510,MONDO:0030428,immunodeficiency 85 and autoimmunity,
+BMGC_DS18558,BMG_DS071328,,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND BRAIN ABNORMALITIES,,,,,,,C5561977,,600580;619512,MONDO:0859187,neurodevelopmental disorder with hypotonia and brain abnormalities,
+BMGC_DS18559,BMG_DS071329,,SPERMATOGENIC FAILURE 56,,,,,DOID:0112336,spermatogenic failure 56,C5561978,,605884;619515,MONDO:0030430,spermatogenic failure 56,
+BMGC_DS18560,BMG_DS071330,,NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ABNORMALITIES,,,,,,,C5561979,,619517;600580,MONDO:0859188,neurodevelopmental disorder with seizures and brain abnormalities,
+BMGC_DS18561,BMG_DS071331,,"MUSCULAR DYSTROPHY, CONGENITAL HEARING LOSS, AND OVARIAN INSUFFICIENCY SYNDROME",,,,,,,C5561980,,606982;619518,MONDO:0859189,"muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome",
+BMGC_DS18562,BMG_DS071332,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2FF",,,,,,,C5561981,,609743;619519,MONDO:0030433,"Charcot-Marie-Tooth disease, axonal, type 2FF",
+BMGC_DS18563,BMG_DS071333,,,,,,,,,C5561983,,619521,MONDO:0030434,"epilepsy, idiopathic generalized, susceptibility to, 18",
+BMGC_DS18564,BMG_DS071334,,NEURODEVELOPMENTAL-CRANIOFACIAL SYNDROME WITH VARIABLE RENAL AND CARDIAC ABNORMALITIES,,,,,,,C5561984,,602221;619522,MONDO:0859190,neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities,
+BMGC_DS18565,BMG_DS071335,,"ANEMIA, SIDEROBLASTIC, 5",,,,,DOID:0061007,sideroblastic anemia 5,C5561985,,619523;608142,MONDO:0030436,"anemia, sideroblastic, 5",
+BMGC_DS18566,BMG_DS071336,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIw",,,,,,,C5561986,,619525;602671,MONDO:0030437,"congenital disorder of glycosylation, type IIw",
+BMGC_DS18567,BMG_DS071337,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 16",,,,,DOID:0112333,pontocerebellar hypoplasia type 16,C5561987,,619527;605391,MONDO:0030438,"pontocerebellar hypoplasia, type 16",
+BMGC_DS18568,BMG_DS071338,,SPERMATOGENIC FAILURE 57,,,,,DOID:0112338,spermatogenic failure 57,C5561988,,619528;619529,MONDO:0030439,spermatogenic failure 57,
+BMGC_DS18569,BMG_DS071339,,CONE-ROD DYSTROPHY 22,,,,,DOID:0081448,cone-rod dystrophy 22,C5561989,,615175;619531,MONDO:0030440,cone-rod dystrophy 22,
+BMGC_DS18570,BMG_DS071340,,"BILIARY, RENAL, NEUROLOGIC, AND SKELETAL SYNDROME",,,,,,,C5561990,,617453;619534,MONDO:0859191,"biliary, renal, neurologic, and skeletal syndrome",
+BMGC_DS18571,BMG_DS071341,,,,,,,,,C5561991,,619538,MONDO:0859192,cerebral cavernous malformation 4,
+BMGC_DS18572,BMG_DS071342,,BOUDIN-MORTIER SYNDROME,,,,,,,C5561992,,108962;619543,MONDO:0859194,Boudin-Mortier syndrome,
+BMGC_DS18573,BMG_DS071343,,"USMANI-RIAZUDDIN SYNDROME, AUTOSOMAL RECESSIVE",,,,,,,C5561994,,603533;619548,MONDO:0859196,"Usmani-Riazuddin syndrome, autosomal recessive",
+BMGC_DS18574,BMG_DS071344,,IMMUNODEFICIENCY 86,,,,,,,C5561995,,619549;608238,MONDO:0030448,immunodeficiency 86,
+BMGC_DS18575,BMG_DS071345,,"DEAFNESS, AUTOSOMAL RECESSIVE 118, WITH COCHLEAR APLASIA",,,,,,,C5561996,,619553,MONDO:0030449,"hearing loss, autosomal recessive 118, with cochlear aplasia",
+BMGC_DS18576,BMG_DS071346,,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA, IMPAIRED SPEECH, AND DYSMORPHIC FACIES",,,,,DOID:0081262,"intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies",C5561997,,619556;603002,MONDO:0859197,"intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies",
+BMGC_DS18577,BMG_DS071347,,"SHORT STATURE, IMPAIRED INTELLECTUAL DEVELOPMENT, MICROCEPHALY, HYPOTONIA, AND OCULAR ANOMALIES",,,,,,,C5561998,,615894;619557,MONDO:0859198,"short stature, impaired intellectual development, microcephaly, hypotonia, and ocular anomalies",
+BMGC_DS18578,BMG_DS071348,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 97,,,,,DOID:0070383,developmental and epileptic encephalopathy 97,C5561999,,602538;619561,MONDO:0030453,developmental and epileptic encephalopathy 97,
+BMGC_DS18579,BMG_DS071349,,JOUBERT SYNDROME 39,,,,,,,C5562000,,619285;619562,MONDO:0030454,Joubert syndrome 39,
+BMGC_DS18580,BMG_DS071350,,DYSTONIA 31,,,,,DOID:0060938,dystonia 31,C5562001,,619600;619565,MONDO:0030455,dystonia 31,
+BMGC_DS18581,BMG_DS071351,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 27",,,,,,,C5562002,,619566;602570,MONDO:0030456,"muscular dystrophy, limb-girdle, autosomal recessive 27",
+BMGC_DS18582,BMG_DS071352,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2HH",,,,,,,C5562003,,619574;601920,MONDO:0030458,"Charcot-Marie-Tooth disease, axonal, Type 2HH",
+BMGC_DS18583,BMG_DS071353,,DEVELOPMENTAL DELAY WITH OR WITHOUT INTELLECTUAL IMPAIRMENT OR BEHAVIORAL ABNORMALITIES,,,,,,,C5562004,,619575,MONDO:0859199,developmental delay with or without intellectual impairment or behavioral abnormalities,
+BMGC_DS18584,BMG_DS071354,,"CEREBELLAR ATAXIA, BRAIN ABNORMALITIES, AND CARDIAC CONDUCTION DEFECTS",,,,,,,C5562005,,619576;606492,MONDO:0859200,"cerebellar ataxia, brain abnormalities, and cardiac conduction defects",
+BMGC_DS18585,BMG_DS071355,,NEURODEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND ATAXIA AND WITH OR WITHOUT SEIZURES,,,,,,,C5562006,,619580,MONDO:0859201,neurodevelopmental disorder with impaired language and ataxia and with or without seizures,
+BMGC_DS18586,BMG_DS071356,,JOUBERT SYNDROME 40,,,,,,,C5562007,,608040;619582,MONDO:0030462,Joubert syndrome 40,
+BMGC_DS18587,BMG_DS071357,,SPERMATOGENIC FAILURE 58,,,,,DOID:0112352,spermatogenic failure 58,C5562008,,608040;619585,MONDO:0030463,spermatogenic failure 58,
+BMGC_DS18588,BMG_DS071358,,"EPIDERMOLYSIS BULLOSA SIMPLEX 2B, GENERALIZED INTERMEDIATE",,,,,,,C5562009,,619588;148040,MONDO:0030525,"epidermolysis bullosa simplex 2B, generalized intermediate",
+BMGC_DS18589,BMG_DS071359,,CATARACT 49,,,,,,,C5562010,,619593,MONDO:0030465,cataract 49,
+BMGC_DS18590,BMG_DS071360,,"EPIDERMOLYSIS BULLOSA SIMPLEX 2C, LOCALIZED",,,,,,,C5562011,,619594;148040,MONDO:0030527,"epidermolysis bullosa simplex 2C, localized",
+BMGC_DS18591,BMG_DS071361,,"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES",,,,,,,C5562012,,619595;611421,MONDO:0859202,"developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities",
+BMGC_DS18592,BMG_DS071362,,"RHIZOMELIC DYSPLASIA, AIN-NAZ TYPE",,,,,,,C5562013,,616510;619598,MONDO:0859203,"rhizomelic dysplasia, Ain-Naz type",
+BMGC_DS18593,BMG_DS071363,,"EPIDERMOLYSIS BULLOSA SIMPLEX 2D, GENERALIZED, INTERMEDIATE OR SEVERE, AUTOSOMAL RECESSIVE",,,,,,,C5562014,,619599,MONDO:0030535,"epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive",
+BMGC_DS18594,BMG_DS071364,,"FETAL AKINESIA, RESPIRATORY INSUFFICIENCY, MICROCEPHALY, POLYMICROGYRIA, AND DYSMORPHIC FACIES",,,,,,,C5562015,,182340;619602,MONDO:0859204,"fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies",
+BMGC_DS18595,BMG_DS071365,,GALLOWAY-MOWAT SYNDROME 9,,,,,,,C5562016,,617436;619603,MONDO:0030471,Galloway-Mowat syndrome 9,
+BMGC_DS18596,BMG_DS071366,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 98,,,,,DOID:0070384,developmental and epileptic encephalopathy 98,C5562017,,619605;182340,MONDO:0030472,developmental and epileptic encephalopathy 98,
+BMGC_DS18597,BMG_DS071367,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 99,,,,,DOID:0070385,developmental and epileptic encephalopathy 99,C5562018,,619606;182350,MONDO:0030473,developmental and epileptic encephalopathy 99,
+BMGC_DS18598,BMG_DS071368,,"HETEROTAXY, VISCERAL, 11, AUTOSOMAL, WITH MALE INFERTILITY",,,,,,,C5562019,,619608;605152,MONDO:0030475,"heterotaxy, visceral, 11, autosomal, with male infertility",
+BMGC_DS18599,BMG_DS071369,,GALLOWAY-MOWAT SYNDROME 10,,,,,,,C5562020,,619609;612276,MONDO:0030476,Galloway-Mowat syndrome 10,
+BMGC_DS18600,BMG_DS071370,,INTERSTITIAL LUNG DISEASE 1,,,,,DOID:0060941,interstitial lung disease 1,C5562021,,178630;619611,MONDO:0030608,interstitial lung disease 1,
+BMGC_DS18601,BMG_DS071371,,RETINITIS PIGMENTOSA 92,,,,,,,C5562022,,619614;617221,MONDO:0030619,retinitis pigmentosa 92,
+BMGC_DS18602,BMG_DS071372,,"DEAFNESS, AUTOSOMAL RECESSIVE 119",,,,,,,C5562023,,619615;619578,MONDO:0030480,"hearing loss, autosomal recessive 119",
+BMGC_DS18603,BMG_DS071373,,NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS AND SPASTICITY,,,,,,,C5562024,,619616;619578,MONDO:0859206,neurodevelopmental disorder with hearing loss and spasticity,
+BMGC_DS18604,BMG_DS071374,,"SPASTIC PARAPLEGIA 84, AUTOSOMAL RECESSIVE",,,,,DOID:0112347,hereditary spastic paraplegia 84,C5562025,,600286;619621,MONDO:0030482,"spastic paraplegia 84, autosomal recessive",
+BMGC_DS18605,BMG_DS071375,,IMMUNODEFICIENCY 88,,,,,,,C5562026,,604895;619630,MONDO:0030483,immunodeficiency 88,
+BMGC_DS18606,BMG_DS071376,,IMMUNODEFICIENCY 89 AND AUTOIMMUNITY,,,,,,,C5562027,,619632;607209,MONDO:0030484,immunodeficiency 89 and autoimmunity,
+BMGC_DS18607,BMG_DS071377,,ACROMESOMELIC DYSPLASIA 4,,,,,DOID:0081238,acromesomelic dysplasia-4,C5562028,,619636;601591,MONDO:0030553,acromesomelic dysplasia 4,
+BMGC_DS18608,BMG_DS071378,,DYSTONIA 32,,,,,DOID:0060939,dystonia 32,C5562029,,608549;619637,MONDO:0030486,dystonia 32,
+BMGC_DS18609,BMG_DS071379,,"SPONDYLOMETAPHYSEAL DYSPLASIA, PAGNAMENTA TYPE",,,,,,,C5562030,,601591;619638,MONDO:0030487,"spondylometaphyseal dysplasia, pagnamenta type",
+BMGC_DS18610,BMG_DS071380,,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND GROSS MOTOR AND SPEECH DELAY,,,,,,,C5562031,,603753;619639,MONDO:0859207,neurodevelopmental disorder with hypotonia and gross motor and speech delay,
+BMGC_DS18611,BMG_DS071381,,HENGEL-MAROOFIAN-SCHOLS SYNDROME,,,,,DOID:0070408,Hengel-Maroofian-Schols syndrome,C5562032,,607470;619641,MONDO:0859208,Hengel-Maroofian-Schols syndrome,
+BMGC_DS18612,BMG_DS071382,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 11,,,,,,,C5562033,,608860;619643,MONDO:0030490,oocyte maturation defect 11,
+BMGC_DS18613,BMG_DS071383,,SPERMATOGENIC FAILURE 59,,,,,DOID:0112357,spermatogenic failure 59,C5562034,,619645;617131,MONDO:0030492,spermatogenic failure 59,
+BMGC_DS18614,BMG_DS071384,,SPERMATOGENIC FAILURE 60,,,,,DOID:0112355,spermatogenic failure 60,C5562035,,617332;619646,MONDO:0030493,spermatogenic failure 60,
+BMGC_DS18615,BMG_DS071385,,"DYSKINESIA WITH OROFACIAL INVOLVEMENT, AUTOSOMAL RECESSIVE",,,,,,,C5562036,,600293;619647,MONDO:0030625,"dyskinesia with orofacial involvement, autosomal recessive",
+BMGC_DS18616,BMG_DS071386,,ZAKI SYNDROME,,,,,DOID:0070473,Zaki syndrome,C5562037,,619648;611514,MONDO:0859209,Zaki syndrome,
+BMGC_DS18617,BMG_DS071387,,NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS AND DYSKINESIA,,,,,,,C5562038,,600293;619651,MONDO:0859211,neurodevelopmental disorder with hyperkinetic movements and dyskinesia,
+BMGC_DS18618,BMG_DS071388,,IMMUNODEFICIENCY 92,,,,,,,C5562039,,164910;619652,MONDO:0030498,immunodeficiency 92,
+BMGC_DS18619,BMG_DS071389,,"NEURODEVELOPMENTAL DISORDER, NONPROGRESSIVE, WITH SPASTICITY AND TRANSIENT OPISTHOTONUS",,,,,,,C5562040,,601995;619653,MONDO:0859212,"neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus",
+BMGC_DS18620,BMG_DS071390,,LOEYS-DIETZ SYNDROME 6,,,,,DOID:0060964,Loeys-Dietz syndrome 6,C5562041,,619656;601366,MONDO:0030500,Loeys-Dietz syndrome 6,
+BMGC_DS18621,BMG_DS071391,,"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 8, WITH OR WITHOUT HETEROTAXY",,,,,,,C5562042,,619657,MONDO:0859213,"congenital heart defects, multiple types, 8, with or without heterotaxy",
+BMGC_DS18622,BMG_DS071392,,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 7, WITH OR WITHOUT HEARING LOSS",,,,,,,C5562043,,619658;617431,MONDO:0030503,"cholestasis, progressive familial intrahepatic, 7, with or without hearing loss",
+BMGC_DS18623,BMG_DS071393,,"LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS 2",,,,,,,C5562044,,619661;601065,MONDO:0030634,"leukoencephalopathy, hereditary diffuse, with spheroids 2",
+BMGC_DS18624,BMG_DS071394,,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 8",,,,,,,C5562045,,611278;619662,MONDO:0030505,"cholestasis, progressive familial intrahepatic, 8",
+BMGC_DS18625,BMG_DS071395,,OVARIAN DYSGENESIS 9,,,,,DOID:0061013,ovarian dysgenesis 9,C5562046,,615384;619665,MONDO:0030506,ovarian dysgenesis 9,
+BMGC_DS18626,BMG_DS071396,,SPERMATOGENIC FAILURE 61,,,,,DOID:0112350,spermatogenic failure 61,C5562048,,619672;608489,MONDO:0030507,spermatogenic failure 61,
+BMGC_DS18627,BMG_DS071397,,SPERMATOGENIC FAILURE 62,,,,,DOID:0112351,spermatogenic failure 62,C5562049,,619673;612041,MONDO:0030508,spermatogenic failure 62,
+BMGC_DS18628,BMG_DS071398,,MARBACH-SCHAAF NEURODEVELOPMENTAL SYNDROME,,,,,,,C5562050,,176911;619680,MONDO:0859214,Marbach-Schaaf neurodevelopmental syndrome,
+BMGC_DS18629,BMG_DS071399,,"DYSTONIA, EARLY-ONSET, AND/OR SPASTIC PARAPLEGIA",,,,,DOID:0070445,early-onset dystonia and/or spastic paraplegia,C5562051,,602736;619681,MONDO:0859215,"dystonia, early-onset, and/or spastic paraplegia",
+BMGC_DS18630,BMG_DS071400,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND NEONATAL CHOLESTASIS",,,,,,,C5562052,,619685;616465,MONDO:0859216,"neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis",
+BMGC_DS18631,BMG_DS071401,,"SPASTIC PARAPLEGIA 85, AUTOSOMAL RECESSIVE",,,,,DOID:0112345,hereditary spastic paraplegia 85,C5562053,,619686;614649,MONDO:0030512,"spastic paraplegia 85, autosomal recessive",
+BMGC_DS18632,BMG_DS071402,,DYSTONIA 33,,,,,DOID:0060940,dystonia 33,C5562054,,176871;619687,MONDO:0030513,dystonia 33,
+BMGC_DS18633,BMG_DS071403,,SPERMATOGENIC FAILURE 63,,,,,DOID:0112356,spermatogenic failure 63,C5562055,,619655;619689,MONDO:0030515,spermatogenic failure 63,
+BMGC_DS18634,BMG_DS071404,,BRUNET-WAGNER NEURODEVELOPMENTAL SYNDROME,,,,,,,C5562056,,180203;619690,MONDO:0859217,Brunet-Wagner neurodevelopmental syndrome,
+BMGC_DS18635,BMG_DS071405,,"TRICHOTHIODYSTROPHY 8, NONPHOTOSENSITIVE",,,,,DOID:0061023,nonphotosensitive trichothiodystrophy 8,C5562057,,619691;601065,MONDO:0030517,"trichothiodystrophy 8, nonphotosensitive",
+BMGC_DS18636,BMG_DS071406,,"TRICHOTHIODYSTROPHY 9, NONPHOTOSENSITIVE",,,,,DOID:0061024,nonphotosensitive trichothiodystrophy 9,C5562058,,619692;156560,MONDO:0030518,"trichothiodystrophy 9, nonphotosensitive",
+BMGC_DS18637,BMG_DS071407,,"AGAMMAGLOBULINEMIA 9, AUTOSOMAL RECESSIVE",,,,,DOID:0081141,agammaglobulinemia 9,C5562059,,601416;619693,MONDO:0030519,"agammaglobulinemia 9, autosomal recessive",
+BMGC_DS18638,BMG_DS071408,,DEVELOPMENTAL DELAY WITH VARIABLE NEUROLOGIC AND BRAIN ABNORMALITIES,,,,,,,C5562060,,619490;619694,MONDO:0859218,developmental delay with variable neurologic and brain abnormalities,
+BMGC_DS18639,BMG_DS071409,,RAUCH-STEINDL SYNDROME,,,,,,,C5562061,,602952;619695,MONDO:0859219,Rauch-Steindl syndrome,
+BMGC_DS18640,BMG_DS071410,,SPERMATOGENIC FAILURE 64,,,,,DOID:0112353,spermatogenic failure 64,C5562062,,609110;619696,MONDO:0030522,spermatogenic failure 64,
+BMGC_DS18641,BMG_DS071411,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 12,,,,,,,C5562063,,619697;609110,MONDO:0030523,oocyte maturation defect 12,
+BMGC_DS18642,BMG_DS071412,,"MUCOPOLYSACCHARIDOSIS, TYPE X",,,,,,,C5562064,,610011;619698,MONDO:0030524,"mucopolysaccharidosis, type 10",
+BMGC_DS18643,BMG_DS071413,,FERGUSON-BONNI NEURODEVELOPMENTAL SYNDROME,,,,,,,C5562065,,606949;619699,MONDO:0859220,Ferguson-Bonni neurodevelopmental syndrome,
+BMGC_DS18644,BMG_DS071414,,YOON-BELLEN NEURODEVELOPMENTAL SYNDROME,,,,,DOID:0070468,Yoon-Bellen neurodevelopmental syndrome,C5562066,,617513;619701,MONDO:0859221,Yoon-Bellen neurodevelopmental syndrome,
+BMGC_DS18645,BMG_DS071415,,SPERMATOGENIC FAILURE 65,,,,,DOID:0112354,spermatogenic failure 65,C5562067,,619712;617277,MONDO:0030531,spermatogenic failure 65,
+BMGC_DS18646,BMG_DS071416,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw, AUTOSOMAL DOMINANT",,,,,,,C5562068,,619714;601134,MONDO:0859223,"congenital disorder of glycosylation, type Iw, autosomal dominant",
+BMGC_DS18647,BMG_DS071417,,"MICROCEPHALY 28, PRIMARY, AUTOSOMAL RECESSIVE",,,,,,,C5562069,,619449;619453,MONDO:0030339,"microcephaly 28, primary, autosomal recessive",
+BMGC_DS18648,BMG_DS071418,,IMMUNODEFICIENCY 87 AND AUTOIMMUNITY,,,,,,,C5562070,,610094;619573,MONDO:0030457,immunodeficiency 87 and autoimmunity,
+BMGC_DS18649,BMG_DS071419,,Sd(a) POLYAGGLUTINATION SYNDROME,,,,,,,C5562071,,615018,,,
+BMGC_DS18650,BMG_DS071420,,"HETEROTAXY, VISCERAL, 10, AUTOSOMAL, WITH MALE INFERTILITY",,,,,,,C5562072,,619607;609804,MONDO:0030474,"heterotaxy, visceral, 10, autosomal, with male infertility",
+BMGC_DS18651,BMG_DS071421,,IMMUNODEFICIENCY 91 AND HYPERINFLAMMATION,,,,,,,C5562073,,618931;619644,MONDO:0030491,immunodeficiency 91 and hyperinflammation,
+BMGC_DS18652,BMG_DS071422,,"LEUKODYSTROPHY, HYPOMYELINATING, 23, WITH ATAXIA, DEAFNESS, LIVER DYSFUNCTION, AND DILATED CARDIOMYOPATHY",,,,,DOID:0070397,hypomyelinating leukodystrophy 23,C5562074,,619688;616136,MONDO:0030514,"leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy",
+BMGC_DS18653,BMG_DS071423,,"CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 1",,,,,,,C5562075,,603851;209880,MONDO:0800026,"central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease",
+BMGC_DS18654,BMG_DS071424,,CHROMOSOME 16q12 DUPLICATION SYNDROME,,,,,,,C5562082,,619649,MONDO:0859210,chromosome 16q12 duplication syndrome,
+BMGC_DS18655,BMG_DS071444,,"ANOSMIA, ISOLATED CONGENITAL, X-LINKED",,,,,,,C5562112,,301700,MONDO:0100469,"anosmia, isolated congenital, X-linked",
+BMGC_DS18656,BMG_DS071446,,"CHROMOSOME 1p36 DELETION SYNDROME, PROXIMAL",,,,,,,C5562114,,619343,MONDO:0859155,"chromosome 1p36 deletion syndrome, proximal",
+BMGC_DS18657,BMG_DS071453,,mmd1 myopathy,,,,,DOID:0070198,Miyoshi muscular dystrophy,C5565781,C537480,,,,
+BMGC_DS18658,BMG_DS071477,1162462009,Angelman syndrome due to maternal monosomy 15q11q13,,,,,,,C5566334,,,MONDO:0020302,Angelman syndrome due to maternal 15q11q13 deletion,Angelman syndrome due to maternal monosomy 15q11q13 (disorder) | Angelman syndrome due to maternal monosomy 15q11q13
+BMGC_DS18659,BMG_DS071499,1162832007,Mayer Rokitansky Küster Hauser syndrome type 1,,,,,,,C5566555,,277000,MONDO:0010173,Mayer-Rokitansky-Kuster-Hauser syndrome type 1,Mayer Rokitansky Küster Hauser syndrome type 1 | Mayer Rokitansky Küster Hauser syndrome type 1 (disorder) | MRKH (Mayer Rokitansky Küster Hauser) syndrome type 1
+BMGC_DS18660,BMG_DS071509,1162916008,Glycogen storage disease due to muscle beta-enolase deficiency,,,,,,,C5566614,,,,,Glycogen storage disease due to muscle beta-enolase deficiency | Glycogenosis type 13 | Muscle enolase deficiency | Glycogen storage disease due to muscle beta-enolase deficiency (disorder) | Glycogenosis due to muscle beta-enolase deficiency | GSDXIII - glycogen storage disease type XIII
+BMGC_DS18661,BMG_DS071649,1167372000,"X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome",,,,,,,C5567226,,,,,"X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome (disorder) | X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome"
+BMGC_DS18662,BMG_DS071650,1167373005,Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder,,,,,DOID:0070474,childhood-onset neurodegeneration with brain atrophy,C5567227,,,,,Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder | Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder (disorder)
+BMGC_DS18663,BMG_DS071652,1169356004,"Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome",,,,,,,C5567229,,617669,MONDO:0044696,early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome,"Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome (disorder) | Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome"
+BMGC_DS18664,BMG_DS071661,1169364005,LRP5-related primary osteoporosis,,,,,,,C5567241,,,MONDO:0044675,LRP5-related primary osteoporosis,Low density lipoprotein receptor-related protein 5 related primary osteoporosis (disorder) | Low density lipoprotein receptor-related protein 5 related primary osteoporosis | LRP5-related primary osteoporosis
+BMGC_DS18665,BMG_DS071703,1172585006,MME-related autosomal dominant Charcot Marie Tooth disease type 2,,,,,,,C5567450,,,MONDO:0044657,MME-related autosomal dominant Charcot Marie Tooth disease type 2,Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 (disorder) | MME-related autosomal dominant Charcot Marie Tooth disease type 2 | Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 | MME-related autosomal dominant hereditary motor and sensory neuropathy type 2
+BMGC_DS18666,BMG_DS071704,1172588008,"Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome",,,,,,,C5567451,,,MONDO:0044651,early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome,"Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome (disorder) | Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome"
+BMGC_DS18667,BMG_DS071705,1172590009,"Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome",,,,,,,C5567452,,,MONDO:0044648,kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome,"Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome | Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome (disorder)"
+BMGC_DS18668,BMG_DS071706,1172591008,"Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome",,,,,,,C5567453,,,MONDO:0044647,kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome,"Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome | Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome (disorder)"
+BMGC_DS18669,BMG_DS071707,1172593006,"Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome",,,,,,,C5567454,,617193,MONDO:0044646,early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome,"Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome (disorder) | Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome"
+BMGC_DS18670,BMG_DS071708,1172594000,"Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome",,,,,,,C5567455,,,MONDO:0044643,congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome,"Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome | Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome (disorder)"
+BMGC_DS18671,BMG_DS071709,1172595004,C11ORF73-related autosomal recessive hypomyelinating leukodystrophy,,,,,,,C5567456,,,MONDO:0044642,c11orf73-related autosomal recessive hypomyelinating leukodystrophy,C11ORF73-related autosomal recessive hypomyelinating leukodystrophy (disorder) | C11ORF73-related autosomal recessive hypomyelinating leukodystrophy | C11ORF73-related autosomal recessive hypomyelinating leucoencephalopathy | C11ORF73-related autosomal recessive hypomyelinating leukoencephalopathy | C11ORF73-related autosomal recessive hypomyelinating leucodystrophy | Hypomyelinating leukodystrophy due to HIKESHI deficiency | Hypomyelinating leucodystrophy due to HIKESHI deficiency
+BMGC_DS18672,BMG_DS071710,1172602000,Childhood-onset benign chorea with striatal involvement,,,,,,,C5567463,,,MONDO:0044332,childhood-onset benign chorea with striatal involvement,Childhood-onset benign chorea with striatal involvement | Childhood-onset benign chorea with striatal involvement (disorder)
+BMGC_DS18673,BMG_DS071711,1172603005,Infantile-onset generalized dyskinesia with orofacial involvement,,,,,,,C5567464,,616921,MONDO:0044637,infantile-onset generalized dyskinesia with orofacial involvement,"Infantile-onset generalised dyskinesia with orofacial involvement | Infantile-onset generalized dyskinesia with orofacial involvement | Infantile-onset generalized dyskinesia with orofacial involvement (disorder) | Infantile-onset orofacial, trunk, limbs dyskinesia"
+BMGC_DS18674,BMG_DS071712,1172604004,"Diaphanous related formin 1 related sensorineural hearing loss, thrombocytopenia syndrome",,,,,,,C5567465,,,MONDO:0044635,DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome,"DIAPH1-related sensorineural deafness, thrombocytopenia syndrome | DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome | Diaphanous related formin 1 related sensorineural hearing loss, thrombocytopenia syndrome | Diaphanous related formin 1 related sensorineural hearing loss, thrombocytopenia syndrome (disorder)"
+BMGC_DS18675,BMG_DS071713,1172605003,"Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome",,,,,,,C5567466,,,,,"Retinitis pigmentosa, deafness, premature aging, short stature, facial dysmorphism syndrome | Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome | Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome (disorder) | Retinitis pigmentosa, hearing loss, premature ageing, short stature, facial dysmorphism syndrome | Retinitis pigmentosa, deafness, premature ageing, short stature, facial dysmorphism syndrome"
+BMGC_DS18676,BMG_DS071715,1172624000,RERE-related neurodevelopmental syndrome,,,,,,,C5567477,,,,,Arginine-glutamic acid dipeptide repeats-related neurodevelopmental syndrome | RERE-related neurodevelopmental syndrome | Arginine-glutamic acid dipeptide repeats-related neurodevelopmental syndrome (disorder)
+BMGC_DS18677,BMG_DS071716,1172625004,DDX41-related hematologic malignancy predisposition syndrome,,,,,,,C5567478,,,,,DDX41-related hematologic malignancy predisposition syndrome | DEAD-box helicase 41-related hematologic malignancy predisposition syndrome | DDX41-related haematologic malignancy predisposition syndrome | DEAD-box helicase 41-related hematologic malignancy predisposition syndrome (disorder) | DEAD-box helicase 41-related haematologic malignancy predisposition syndrome
+BMGC_DS18678,BMG_DS071717,1172627007,"Early-onset epilepsy, intellectual disability, brain anomalies syndrome",,,,,,,C5567479,,,,,"Early-onset epilepsy, intellectual disability, brain anomalies syndrome | Congenital disorder of glycosylation due to PIGG (phosphatidylinositol glycan anchor biosynthesis class G) deficiency | PIGG-CDG - congenital disorder of glycosylation due to PIGG deficiency | Congenital disorder of glycosylation due to phosphatidylinositol glycan anchor biosynthesis class G deficiency | Early-onset epilepsy, intellectual disability, brain anomalies syndrome (disorder)"
+BMGC_DS18679,BMG_DS071718,1172628002,TBCK-related intellectual disability syndrome,,,,,DOID:0060935,infantile hypotonia with psychomotor retardation and characteristic facies-3,C5567480,,616900,MONDO:0014823,"hypotonia, infantile, with psychomotor retardation and characteristic facies 3",TBCK-related intellectual disability syndrome | TBC1 domain containing kinase-related intellectual disability syndrome | TBC1 domain containing kinase-related intellectual disability syndrome (disorder)
+BMGC_DS18680,BMG_DS071719,1172629005,"Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome",,,,,,,C5567481,,,,,"Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome | Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome (disorder)"
+BMGC_DS18681,BMG_DS071720,1172630000,"Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome",,,,,,,C5567482,,,MONDO:0024252,obsolete global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome,"Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome | Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome (disorder)"
+BMGC_DS18682,BMG_DS071721,1172631001,Autosomal recessive spastic paraplegia type 76,,,,,,,C5567483,,616907,MONDO:0014827,autosomal recessive spastic paraplegia type 76,Autosomal recessive spastic paraplegia type 76 (disorder) | Autosomal recessive spastic paraplegia type 76
+BMGC_DS18683,BMG_DS071722,1172632008,SIX2-related frontonasal dysplasia,,,,,,,C5567484,,,MONDO:0044628,six2-related frontonasal dysplasia,SIX homeobox 2-related frontonasal dysplasia (disorder) | SIX2-related frontonasal dysplasia | SIX homeobox 2-related frontonasal dysplasia
+BMGC_DS18684,BMG_DS071723,1172634009,Autosomal dominant Charcot-Marie-Tooth disease type 2W,,,,,,,C5567486,,616625,MONDO:0014711,autosomal dominant Charcot-Marie-Tooth disease type 2W,Autosomal dominant Charcot-Marie-Tooth disease type 2W | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS mutation | Autosomal dominant Charcot-Marie-Tooth disease type 2W (disorder) | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS (histidyl-tRNA synthetase 1) mutation
+BMGC_DS18685,BMG_DS071724,1172635005,"Split-foot malformation, mesoaxial polydactyly syndrome",,,,,,,C5567487,,616890,MONDO:0014816,split-foot malformation-mesoaxial polydactyly syndrome,"SFMMP (split-foot malformation, mesoaxial polydactyly) syndrome | Split-foot malformation, mesoaxial polydactyly syndrome | Split-foot malformation, mesoaxial polydactyly syndrome (disorder) | Split-foot malformation, mesoaxial polydactyly, nail abnormalities, sensorineural hearing loss syndrome"
+BMGC_DS18686,BMG_DS071726,,,,,,,,,C5567489,,,MONDO:0044626,female infertility due to oocyte meiotic arrest,
+BMGC_DS18687,BMG_DS071730,1172683008,"Microcephaly, congenital cataract, psoriasiform dermatitis syndrome",,,,,,,C5567510,,616834,MONDO:0014793,microcephaly-congenital cataract-psoriasiform dermatitis syndrome,"Sterol-C4-methyl oxidase deficiency | SMO (sterol-C4-methyl oxidase) deficiency | Microcephaly, congenital cataract, psoriasiform dermatitis syndrome | Microcephaly, congenital cataract, psoriasiform dermatitis syndrome (disorder)"
+BMGC_DS18688,BMG_DS071731,1172684002,Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation,,,,,,,C5567515,,,MONDO:0044625,autosomal dominant charcot-marie-tooth disease type 2 due to DGAT2 mutation,Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to diacylglycerol O-acyltransferase 2 mutation (disorder) | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to diacylglycerol O-acyltransferase 2 mutation
+BMGC_DS18689,BMG_DS071732,1172689007,Prenatal-onset spinal muscular atrophy with congenital bone fractures,,,,,,,C5567518,,,MONDO:0000209,prenatal-onset spinal muscular atrophy with congenital bone fractures,Prenatal-onset spinal muscular atrophy with congenital bone fractures (disorder) | Prenatal-onset spinal muscular atrophy with congenital bone fractures
+BMGC_DS18690,BMG_DS071734,1172692006,"X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome",,,,,,,C5567520,,,MONDO:0044617,X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome,"X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome | X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome (disorder)"
+BMGC_DS18691,BMG_DS071735,1172694007,Adenylosuccinate synthetase-like 1-related distal myopathy,,,,,,,C5567521,,617030,MONDO:0014877,"myopathy, distal, 5",ADSSL1-related distal myopathy | Adenylosuccinate synthetase-like 1-related distal myopathy (disorder) | Adenylosuccinate synthetase-like 1-related distal myopathy
+BMGC_DS18692,BMG_DS071736,1172696009,"Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome",,,,,,,C5567522,,,MONDO:0018822,global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome,"Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder) | Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome"
+BMGC_DS18693,BMG_DS071737,1172697000,"X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability",,,,,,,C5567523,,,MONDO:0018821,X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability,"X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability | X-linked facial dysmorphism, short stature, choanal atresia, intellectual disability syndrome limited to females | X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability (disorder)"
+BMGC_DS18694,BMG_DS071738,1172698005,"Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome",,,,,,,C5567524,,616878,MONDO:0018820,recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome,"Transport and golgi organization 2 homolog-related metabolic encephalopathy, arrhythmia syndrome | Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder) | TANGO2-related metabolic encephalopathy, arrhythmia syndrome | Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome | Transport and golgi organisation 2 homolog-related metabolic encephalopathy, arrhythmia syndrome"
+BMGC_DS18695,BMG_DS071741,1172705006,"Lethal hydranencephaly, diaphragmatic hernia syndrome",,,,,,,C5567527,,,MONDO:0018810,lethal hydranencephaly-diaphragmatic hernia syndrome,"Lethal hydranencephaly, diaphragmatic hernia syndrome (disorder) | Lethal hydranencephaly, diaphragmatic hernia syndrome"
+BMGC_DS18696,BMG_DS071744,1172839002,"Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome",,,,,,,C5567603,,,,,"Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome | Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome (disorder)"
+BMGC_DS18697,BMG_DS071745,1172841001,Combined oxidative phosphorylation defect type 30,,,,,,,C5567605,,616974,MONDO:0014856,combined oxidative phosphorylation defect type 30,Combined oxidative phosphorylation defect type 30 | Combined oxidative phosphorylation defect type 30 (disorder) | COXPD30 - combined oxidative phosphorylation defect type 30
+BMGC_DS18698,BMG_DS071746,1172843003,Combined oxidative phosphorylation defect type 29,,,,,,,C5567607,,616811,MONDO:0014781,combined oxidative phosphorylation deficiency 29,Combined oxidative phosphorylation defect type 29 | COXPD29 - combined oxidative phosphorylation defect type 29 | Combined oxidative phosphorylation defect type 29 (disorder)
+BMGC_DS18699,BMG_DS071747,1172844009,Combined oxidative phosphorylation defect type 27,,,,,,,C5567608,,616672,MONDO:0014728,combined oxidative phosphorylation defect type 27,Combined oxidative phosphorylation defect type 27 | Combined oxidative phosphorylation defect type 27 (disorder) | COXPD27 - combined oxidative phosphorylation defect type 27
+BMGC_DS18700,BMG_DS071748,1172889005,"Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome",,,,,,,C5567644,,,,,"Palatal anomalies, multiple diastemata, facial dysmorphism, developmental delay syndrome | Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome | Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome (disorder)"
+BMGC_DS18701,BMG_DS071749,1172892009,Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RORgamma receptor mutation,,,,,,,C5567647,,616622,MONDO:0014710,autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency,Autosomal recessive primary immunodeficiency due to RORC mutation | Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RAR related orphan receptor C receptor mutation (disorder) | Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RORgamma receptor mutation | Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RAR related orphan receptor C receptor mutation | Autosomal recessive MSMD (mendelian susceptibility to mycobacterial disease) due to complete RORgamma receptor mutation
+BMGC_DS18702,BMG_DS071750,1172900005,"Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome",,,,,,,C5567650,,616632,MONDO:0014714,progressive microcephaly-seizures-cortical blindness-developmental delay syndrome,"Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome (disorder)"
+BMGC_DS18703,BMG_DS071751,1172901009,Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder,,,,,,,C5567651,,618372,MONDO:0018794,cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder,Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | PLA2G4A (phospholipase A2 group IVA) related platelet dysfunction | PLA2G4A-related platelet dysfunction | Platelet dysfunction due to cytosolic phospholipase-A2 alpha deficiency | Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
+BMGC_DS18704,BMG_DS071758,1173034002,Combined oxidative phosphorylation defect type 26,,,,,,,C5567741,,616539,MONDO:0014684,combined oxidative phosphorylation defect type 26,Combined oxidative phosphorylation defect type 26 | Combined oxidative phosphorylation defect type 26 (disorder) | COXPD26 - combined oxidative phosphorylation defect type 26
+BMGC_DS18705,BMG_DS071759,1173035001,Combined oxidative phosphorylation defect type 25,,,,,,,C5567742,,616430,MONDO:0014636,combined oxidative phosphorylation defect type 25,Combined oxidative phosphorylation defect type 25 (disorder) | Combined oxidative phosphorylation defect type 25 | COXPD25 - combined oxidative phosphorylation defect type 25
+BMGC_DS18706,BMG_DS071760,1173036000,Combined oxidative phosphorylation defect type 23,,,,,,,C5567743,,616198,MONDO:0014525,combined oxidative phosphorylation defect type 23,Combined oxidative phosphorylation defect type 23 | Combined oxidative phosphorylation defect type 23 (disorder) | COXPD23 - combined oxidative phosphorylation defect type 23
+BMGC_DS18707,BMG_DS071762,1173998003,"Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome",,,,,DOID:0070542,neurodevelopmental disorder with spastic paraplegia and microcephaly,C5567787,,,,,"Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome | Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome (disorder)"
+BMGC_DS18708,BMG_DS071763,1173999006,IL21-related infantile inflammatory bowel disease,,,,,,,C5567788,,615767,MONDO:0014338,IL21-related infantile inflammatory bowel disease,Interleukin 21 related infantile inflammatory bowel disease (disorder) | IL21-related infantile inflammatory bowel disease | Interleukin 21 related infantile inflammatory bowel disease
+BMGC_DS18709,BMG_DS071764,1174000008,Congenital generalized hypercontractile muscle stiffness syndrome,,,,,,,C5567789,,,MONDO:0018780,congenital generalized hypercontractile muscle stiffness syndrome,Congenital generalized hypercontractile muscle stiffness syndrome | Congenital generalised hypercontractile muscle stiffness syndrome | Congenital generalized hypercontractile muscle stiffness syndrome (disorder)
+BMGC_DS18710,BMG_DS071770,1176997000,Methicillin resistant Staphylococcus aureus skin infection,,,,,,,C5567802,,,,,Skin infection caused by Methicillin resistant Staphylococcus aureus (disorder) | Skin infection caused by Methicillin resistant Staphylococcus aureus | Methicillin resistant Staphylococcus aureus skin infection | MRSA (Methicillin resistant Staphylococcus aureus) skin infection
+BMGC_DS18711,BMG_DS071810,1177165005,PMP2-related Charcot-Marie-Tooth disease type 1,,,,,,,C5567891,,,,,PMP2-related Charcot-Marie-Tooth disease type 1 | Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 1 (disorder) | Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 1 | PMP2-related Charcot-Marie-Tooth neuropathy type 1 | PMP2-related hereditary motor and sensory neuropathy type 1
+BMGC_DS18712,BMG_DS071812,1177168007,Autosomal recessive spastic paraplegia type 78,,,,,,,C5567893,,617225,MONDO:0014975,autosomal recessive spastic paraplegia type 78,Autosomal recessive spastic paraplegia type 78 (disorder) | Autosomal recessive spastic paraplegia type 78 | SPG78 - autosomal recessive spastic paraplegia type 78
+BMGC_DS18713,BMG_DS071816,1177173001,"Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome",,,,,,,C5567897,,,MONDO:0033683,congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome,"Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome (disorder) | MYSM1 deficiency | Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome | MYSM1 (Myb like, SWIRM and MPN domains 1) deficiency"
+BMGC_DS18714,BMG_DS071818,1177175008,"Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome",,,,,,,C5567899,,,MONDO:0033682,skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome,"Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome (disorder) | EXTL3 (exostosin like glycosyltransferase 3) related neuro-immuno-skeletal dysplasia syndrome | Neuro-immuno-skeletal dysplasia syndrome due to EXTL3 (exostosin like glycosyltransferase 3) deficiency | Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome | EXTL3-related neuro-immuno-skeletal dysplasia syndrome | Neuro-immuno-skeletal dysplasia syndrome due to EXTL3 deficiency"
+BMGC_DS18715,BMG_DS071819,1177177000,Hyperphenylalaninemia due to DNAJC12 deficiency,,,,,,,C5567900,,,,,Hyperphenylalanineaemia due to DNAJC12 deficiency | Hyperphenylalaninemia due to DNAJC12 deficiency | Hyperphenylalaninemia due to DnaJ heat shock protein family (Hsp40) member C12 deficiency | Hyperphenylalaninemia due to DnaJ heat shock protein family (Hsp40) member C12 deficiency (disorder) | Hyperphenylalanineaemia due to DnaJ heat shock protein family (Hsp40) member C12 deficiency | Non-phenylketonuric non-BH4-deficiency hyperphenylalaninemia | Non-phenylketonuric non-BH4-deficiency hyperphenylalanineaemia
+BMGC_DS18716,BMG_DS071820,1177178005,"Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome",,,,,,,C5567901,,,MONDO:0034991,intrauterine growth restriction-congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome,"Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome (disorder) | Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome"
+BMGC_DS18717,BMG_DS071822,1177179002,Oral-facial-digital syndrome with short stature and brachymesophalangia,,,,,,,C5567903,,617927,MONDO:0054770,orofaciodigital syndrome 18,OFD18 - oral-facial-digital syndrome type 18 | Orofaciodigital syndrome type 18 | Oral-facial-digital syndrome with short stature and brachymesophalangia | Oral-facial-digital syndrome with short stature and brachymesophalangia (disorder)
+BMGC_DS18718,BMG_DS071851,1179282009,"Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract",,,,,,,C5568106,,,,,"Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract | Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract (disorder)"
+BMGC_DS18719,BMG_DS071852,1179283004,"Metopic ridging, ptosis, facial dysmorphism syndrome",,,,,,,C5568107,,618619,MONDO:0032836, | Weiss-Kruszka syndrome,"Metopic ridging, ptosis, facial dysmorphism syndrome | Metopic ridging, ptosis, facial dysmorphism syndrome (disorder)"
+BMGC_DS18720,BMG_DS071853,1179285006,Combined immunodeficiency due to moesin deficiency,,,,,,,C5568123,,300988,MONDO:0010514,combined immunodeficiency due to moesin deficiency,X-linked moesin-associated immunodeficiency | Combined immunodeficiency due to moesin deficiency (disorder) | MSN (moesin) related combined immunodeficiency | Combined immunodeficiency due to moesin deficiency
+BMGC_DS18721,BMG_DS071854,1179286007,Combined immunodeficiency due to GINS1 deficiency,,,,,,,C5568132,,617827,MONDO:0044725,combined immunodeficiency due to GINS1 deficiency,"Combined immunodeficiency due to GINS1 (GINS complex subunit 1) deficiency | Combined immunodeficiency due to GINS complex subunit 1 deficiency | Combined immunodeficiency due to GINS complex subunit 1 deficiency (disorder) | Combined immunodeficiency due to GINS1 deficiency | Combined immunodeficiency with intrauterine growth retardation, NK (natural killer) cell deficiency, neutropenia"
+BMGC_DS18722,BMG_DS071855,1179288008,Combined immunodeficiency due to TFRC deficiency,,,,,DOID:0111948,immunodeficiency 46,C5568133,,616740,MONDO:0014760,TFRC-related combined immunodeficiency,Combined immunodeficiency due to transferrin receptor deficiency (disorder) | Combined immunodeficiency due to transferrin receptor deficiency | TFRC (transferrin receptor) related combined immunodeficiency | Combined immunodeficiency due to TFRC deficiency
+BMGC_DS18723,BMG_DS071856,1179293006,Erythrokeratodermia cardiomyopathy syndrome,,,,,,,C5568136,,,,,Erythrokeratodermia cardiomyopathy syndrome | Erythrokeratodermia cardiomyopathy syndrome (disorder) | EKC (erythrokeratodermia cardiomyopathy) syndrome
+BMGC_DS18724,BMG_DS071857,1179294000,"Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome",,,,,,,C5568137,,,MONDO:0018773,autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome,"Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome | Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome (disorder)"
+BMGC_DS18725,BMG_DS071858,1179295004,BVES-related limb girdle muscular dystrophy,,,,,,,C5568138,,616812,MONDO:0014782,autosomal recessive limb-girdle muscular dystrophy type 2X,"Autosomal recessive limb girdle muscular dystrophy, cardiac arrhythmia syndrome | Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder) | Limb girdle muscular dystrophy 2X | BVES-related limb girdle muscular dystrophy | Blood vessel epicardial substance related limb girdle muscular dystrophy | BVES (blood vessel epicardial substance) related limb girdle muscular dystrophy"
+BMGC_DS18726,BMG_DS071859,1179298002,Familial patent arterial duct,,,,,,,C5568140,,,,,Familial patent arterial duct | Familial patent arterial duct (disorder) | Familial PDA (patent ductus arteriosus)
+BMGC_DS18727,BMG_DS071860,1179299005,NEK9-related lethal skeletal dysplasia,,,,,,,C5568141,,617022,MONDO:0014870,NEK9-related lethal skeletal dysplasia,"NEK9-related lethal skeletal dysplasia | NIMA related kinase 9 lethal skeletal dysplasia (disorder) | NIMA related kinase 9 lethal skeletal dysplasia | Lethal skeletal dysplasia, foetal akinesia, contractures, thoracic dysplasia, pulmonary hypoplasia syndrome | Lethal skeletal dysplasia, fetal akinesia, contractures, thoracic dysplasia, pulmonary hypoplasia syndrome"
+BMGC_DS18728,BMG_DS071861,,,,,,,,,C5568143,,614104,MONDO:0013578,DYRK1A-related intellectual disability syndrome,
+BMGC_DS18729,BMG_DS071903,1186654001,"Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome",,,,,,,C5568533,,,MONDO:0033968,immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome,"Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome (disorder) | Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome"
+BMGC_DS18730,BMG_DS071905,1186712009,Combined immunodeficiency due to CARMIL2 deficiency,,,,,,,C5568557,,,,,Combined immunodeficiency due to CARMIL2 deficiency | Combined immunodeficiency due to capping protein regulator and myosin 1 linker 2 deficiency (disorder) | Combined immunodeficiency due to capping protein regulator and myosin 1 linker 2 deficiency | Combined immunodeficiency due to RLTPR deficiency
+BMGC_DS18731,BMG_DS071906,1186713004,"Growth delay, intellectual disability, hepatopathy syndrome",,,,,,,C5568558,,,,,"Growth delay, intellectual disability, hepatopathy syndrome | Growth delay, intellectual disability, hepatopathy syndrome (disorder)"
+BMGC_DS18732,BMG_DS071907,1186715006,Combined immunodeficiency due to CD70 deficiency,,,,,,,C5568559,,618261,MONDO:0034054,severe combined immunodeficiency due to CD70 deficiency,Combined immunodeficiency due to CD70 deficiency (disorder) | Combined immunodeficiency due to CD70 deficiency
+BMGC_DS18733,BMG_DS071908,1186718008,"Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome",,,,,,,C5568562,,616276,MONDO:0014562,neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome,"Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome (disorder) | Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome | Coenzyme Q4-related neonatal encephalomyopathy | COQ4-related neonatal encephalomyopathy"
+BMGC_DS18734,BMG_DS071909,1186720006,"CEBPE-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome",,,,,,,C5568564,,,MONDO:0035437,CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome,"CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome (disorder) | CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | CAIN (CEBPE-associated autoinflammation, immunodeficiency, neutrophil dysfunction) syndrome | CEBPE-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome"
+BMGC_DS18735,BMG_DS071912,1186724002,HTRA1-related autosomal dominant cerebral small vessel disease,,,,,,,C5568568,,,MONDO:0018832,HTRA1-related autosomal dominant cerebral small vessel disease,HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | HTRA1-related autosomal dominant cerebral small vessel disease | HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease | HTRA1-related autosomal dominant cerebral angiopathy
+BMGC_DS18736,BMG_DS071916,1186729007,"Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome",,,,,,,C5568572,,,MONDO:0034989,intellectual disability-cardiac anomalies-short stature-joint laxity syndrome,"Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome (disorder) | Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome"
+BMGC_DS18737,BMG_DS071917,1186734006,Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction,,,,,,,C5568576,,,MONDO:0044737,autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction,Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder) | Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction
+BMGC_DS18738,BMG_DS071934,1186856001,Atypical pantothenate kinase associated neurodegeneration,,,,,,,C5568621,,,MONDO:0016305,atypical pantothenate kinase-associated neurodegeneration,Atypical pantothenate kinase associated neurodegeneration (disorder) | Atypical pantothenate kinase associated neurodegeneration
+BMGC_DS18739,BMG_DS071992,,,,,,,,,C5568766,,,MONDO:0100038,complex neurodevelopmental disorder,
+BMGC_DS18740,BMG_DS071994,1187040004,Familial steroid-resistant nephrotic syndrome with adrenal insufficiency,,,,,,,C5568768,,,,,"Familial steroid-resistant nephrotic syndrome with adrenal insufficiency | Familial steroid-resistant nephrotic syndrome with adrenal insufficiency (disorder) | Primary adrenal insufficiency, steroid-resistant nephrotic syndrome due to SGPL1 deficiency | Primary adrenal insufficiency, steroid-resistant nephrotic syndrome due to SGPL1 (sphingosine-1-phosphate lyase 1) deficiency"
+BMGC_DS18741,BMG_DS071995,1187041000,"STAG1-related intellectual disability, facial dysmorphism, gastroesophageal reflux syndrome",,,,,,,C5568769,,,,,"Stromal antigen 1-related intellectual disability, facial dysmorphism, gastroesophageal reflux syndrome | STAG1-related intellectual disability, facial dysmorphism, gastrooesophageal reflux syndrome | Stromal antigen 1-related intellectual disability, facial dysmorphism, gastrooesophageal reflux syndrome | STAG1-related intellectual disability, facial dysmorphism, gastroesophageal reflux syndrome | Stromal antigen 1-related intellectual disability, facial dysmorphism, gastroesophageal reflux syndrome (disorder)"
+BMGC_DS18742,BMG_DS071996,1187042007,"Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome",,,,,,,C5568770,,,,,"Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome | Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome (disorder)"
+BMGC_DS18743,BMG_DS071997,1187043002,"Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome",,,,,,,C5568771,,,,,"Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome (disorder) | Cerebrorenal syndrome Perez type | Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome"
+BMGC_DS18744,BMG_DS072003,1187113001,Mucopolysaccharidosis-like plus disease,,,,,,,C5568800,,,,,Mucopolysaccharidosis-like syndrome with congenital heart defect and hematopoietic disorder | Mucopolysaccharidosis-like syndrome with congenital heart defect and haematopoietic disorder | Mucopolysaccharidosis-like plus disease | Mucopolysaccharidosis-like plus disease (disorder)
+BMGC_DS18745,BMG_DS072004,1187114007,"Micrognathia, recurrent infections, behavioral abnormalities, mild intellectual disability syndrome",,,,,,,C5568801,,,,,"Micrognathia, recurrent infections, behavioural abnormalities, mild intellectual disability syndrome | Micrognathia, recurrent infections, behavioral abnormalities, mild intellectual disability syndrome (disorder) | Micrognathia, recurrent infections, behavioral abnormalities, mild intellectual disability syndrome"
+BMGC_DS18746,BMG_DS072005,1187115008,"Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome",,,,,,,C5568802,,,MONDO:0018777,autosomal dominant preaxial polydactyly-upperback hypertrichosis syndrome,"Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome (disorder) | Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome"
+BMGC_DS18747,BMG_DS072017,1187178004,Isolated generalized anhidrosis with normal sweat glands,,,,,,,C5568836,,106190,MONDO:0007118,isolated anhidrosis with normal sweat glands,Isolated generalized anhidrosis with normal sweat glands | Isolated generalised anhidrosis with normal sweat glands | Isolated generalized anhidrosis with normal sweat glands (disorder)
+BMGC_DS18748,BMG_DS072018,1187191003,Autosomal recessive spastic paraplegia type 74,,,,,,,C5568837,,616451,MONDO:0014644,hereditary spastic paraplegia 74,Autosomal recessive spastic paraplegia type 74 | Autosomal recessive spastic paraplegia type 74 (disorder)
+BMGC_DS18749,BMG_DS072019,1187194006,Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene,,,,,,,C5568838,,,MONDO:0018766,chronic enteropathy associated with SLCO2A1 gene,Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene | Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder) | Chronic enteropathy associated with SLCO2A1 gene
+BMGC_DS18750,BMG_DS072021,1187210007,"Intellectual disability, epilepsy, extrapyramidal syndrome",,,,,,,C5568848,,,,,"Intellectual disability, epilepsy, extrapyramidal syndrome | Intellectual disability, epilepsy, extrapyramidal syndrome (disorder)"
+BMGC_DS18751,BMG_DS072022,1187212004,"Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome",,,,,,,C5568849,,,,,"Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome (disorder) | Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome"
+BMGC_DS18752,BMG_DS072023,,,,,,,,,C5568850,,,MONDO:0018763,tubulinopathy-associated dysgyria,
+BMGC_DS18753,BMG_DS072025,1187252002,Autosomal dominant thrombocytopenia with platelet secretion defect,,,,,,,C5568864,,,,,Autosomal dominant thrombocytopenia with platelet secretion defect | Autosomal dominant thrombocytopenia with platelet secretion defect (disorder)
+BMGC_DS18754,BMG_DS072027,1187277001,"Short stature, brachydactyly, obesity, global developmental delay syndrome",,,,,,,C5568868,,,,,"Short stature, brachydactyly, obesity, global developmental delay syndrome | Short stature, brachydactyly, obesity, global developmental delay syndrome (disorder) | SBIDDS - short stature, brachydactyly, impaired intellectual development, seizures"
+BMGC_DS18755,BMG_DS072028,1187278006,"Spastic paraplegia, severe developmental delay, epilepsy syndrome",,,,,,,C5568869,,,,,"SPPRS (spastic paraplegia, psychomotor retardation, seizures) syndrome | Spastic paraplegia, severe developmental delay, epilepsy syndrome | Spastic paraplegia, severe developmental delay, epilepsy syndrome (disorder)"
+BMGC_DS18756,BMG_DS072029,1186711002,"GNB5-related intellectual disability, cardiac arrhythmia syndrome",,,,,,,C5568877,,617173,MONDO:0014953,gnb5-related intellectual disability-cardiac arrhythmia syndrome,"GNB5-related intellectual disability, cardiac arrhythmia syndrome | G protein subunit beta 5-related intellectual disability, cardiac arrhythmia syndrome | G protein subunit beta 5-related intellectual disability, cardiac arrhythmia syndrome (disorder)"
+BMGC_DS18757,BMG_DS072030,1187249005,VPS11-related autosomal recessive hypomyelinating leukodystrophy,,,,,,,C5568878,,,,,VPS11-related autosomal recessive hypomyelinating leukodystrophy | VPS11-related autosomal recessive hypomyelinating leucodystrophy | VPS11-related autosomal recessive hypomyelinating leukoencephalopathy | VPS11-related autosomal recessive hypomyelinating leucoencephalopathy | VPS11 core subunit of CORVET and HOPS complexes-related autosomal recessive hypomyelinating leukodystrophy (disorder) | VPS11 core subunit of CORVET and HOPS complexes-related autosomal recessive hypomyelinating leucodystrophy | VPS11 core subunit of CORVET and HOPS complexes-related autosomal recessive hypomyelinating leukodystrophy
+BMGC_DS18758,BMG_DS072031,1187303004,"Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome",,,,,,,C5568882,,616723,MONDO:0014748,progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome,"Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome | Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome (disorder)"
+BMGC_DS18759,BMG_DS072032,1187462006,Glycogen storage disease due to phosphoglycerate kinase 1 deficiency,,,,,,,C5568976,,,,,Glycogen storage disease due to phosphoglycerate kinase 1 deficiency | Glycogen storage disease due to phosphoglycerate kinase 1 deficiency (disorder) | Glycogenosis due to phosphoglycerate kinase 1 deficiency
+BMGC_DS18760,BMG_DS072033,1187465008,Autosomal dominant spastic paraplegia type 9A,,,,,,,C5568978,,601162,MONDO:0011006,hereditary spastic paraplegia 9A,"Cataracts, motor neuropathy, short stature, skeletal anomalies syndrome | Autosomal dominant spastic paraplegia type 9A | Autosomal dominant spastic paraplegia type 9A (disorder) | Spastic paraparesis, amyotrophy, cataracts, gastroesophageal reflux syndrome | Spastic paraparesis, amyotrophy, cataracts, gastro-oesophageal reflux syndrome"
+BMGC_DS18761,BMG_DS072034,1187466009,Autosomal dominant spastic paraplegia type 9B,,,,,,,C5568979,,,MONDO:0018644,autosomal dominant complex spastic paraplegia type 9B,Autosomal dominant spastic paraplegia type 9B | Autosomal dominant spastic paraplegia type 9B (disorder)
+BMGC_DS18762,BMG_DS072035,1187467000,Autosomal recessive spastic paraplegia type 9B,,,,,,,C5568980,,616586,MONDO:0014702,autosomal recessive complex spastic paraplegia type 9B,Autosomal recessive spastic paraplegia type 9B | Autosomal recessive spastic paraplegia type 9B (disorder)
+BMGC_DS18763,BMG_DS072036,1187468005,Autosomal dominant spastic paraplegia type 73,,,,,,,C5568981,,616282,MONDO:0014568,hereditary spastic paraplegia 73,Autosomal dominant spastic paraplegia type 73 | Autosomal dominant spastic paraplegia type 73 (disorder)
+BMGC_DS18764,BMG_DS072037,1187506008,Autosomal recessive spastic paraplegia type 77,,,,,,,C5569007,,617046,MONDO:0014882,hereditary spastic paraplegia 77,Autosomal recessive spastic paraplegia type 77 | Autosomal recessive spastic paraplegia type 77 (disorder)
+BMGC_DS18765,BMG_DS072053,1187563003,Autosomal recessive Charcot-Marie-Tooth disease type 2X,,,,,,,C5569024,,616668,MONDO:0014726,Charcot-Marie-Tooth disease axonal type 2X,"Autosomal recessive Charcot-Marie-Tooth disease type 2X | Autosomal recessive Charcot-Marie-Tooth disease type 2X (disorder) | Autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 (SPG11 vesicle trafficking associated, spatacsin) mutation | Autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation"
+BMGC_DS18766,BMG_DS072054,1187564009,Autosomal dominant Charcot-Marie-Tooth disease type 2Z,,,,,,,C5569025,,616688,MONDO:0014736,Charcot-Marie-Tooth disease axonal type 2Z,Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MORC2 mutation | Autosomal dominant Charcot-Marie-Tooth disease type 2Z | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MORC2 (MORC family CW-type zinc finger 2) mutation | Autosomal dominant Charcot-Marie-Tooth disease type 2Z (disorder)
+BMGC_DS18767,BMG_DS072055,1187565005,Autosomal dominant Charcot-Marie-Tooth disease type 2Y,,,,,,,C5569026,,616687,MONDO:0014735,Charcot-Marie-Tooth disease type 2Y,Autosomal dominant Charcot-Marie-Tooth disease type 2Y | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation | Autosomal dominant Charcot-Marie-Tooth disease type 2Y (disorder) | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP (valosin containing protein) mutation
+BMGC_DS18768,BMG_DS072056,1187567002,Autosomal recessive intermediate Charcot-Marie-Tooth disease type D,,,,,,,C5569027,,616039,MONDO:0014467,Charcot-Marie-Tooth disease recessive intermediate D,Autosomal recessive intermediate Charcot-Marie-Tooth disease type D (disorder) | Autosomal recessive intermediate Charcot-Marie-Tooth disease type D
+BMGC_DS18769,BMG_DS072057,1187566006,Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation,,,,,,,C5569028,,,MONDO:0018567,autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation,Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to trafficking from endoplasmic reticulum to golgi regulator mutation (disorder) | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to trafficking from endoplasmic reticulum to golgi regulator mutation
+BMGC_DS18770,BMG_DS072058,1187614006,Severe autosomal recessive macrothrombocytopenia,,,,,,,C5569048,,,,,Severe autosomal recessive macrothrombocytopenia (disorder) | Severe autosomal recessive macrothrombocytopenia
+BMGC_DS18771,BMG_DS072059,1187618009,Autosomal dominant Charcot-Marie-Tooth disease type 2V,,,,,,,C5569050,,616491,MONDO:0014665,Charcot-Marie-Tooth disease axonal type 2V,Autosomal dominant Charcot-Marie-Tooth disease type 2V (disorder) | Autosomal dominant Charcot-Marie-Tooth disease type 2V | Hereditary adult onset painful axonal polyneuropathy | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU (N-acetyl-alpha-glucosaminidase) mutation
+BMGC_DS18772,BMG_DS072060,1187619001,Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect,,,,,,,C5569051,,,MONDO:0033850,autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect,Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect (disorder) | Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect
+BMGC_DS18773,BMG_DS072061,1187621006,DNAJB2-related Charcot-Marie-Tooth disease type 2,,,,,,,C5569053,,,,,DNAJB2-related Charcot-Marie-Tooth disease type 2 | DnaJ heat shock protein family (Hsp40) member B2-related Charcot-Marie-Tooth disease type 2 (disorder) | DnaJ heat shock protein family (Hsp40) member B2-related Charcot-Marie-Tooth disease type 2
+BMGC_DS18774,BMG_DS072085,1187640000,Combined oxidative phosphorylation defect type 28,,,,,,,C5569081,,616794,MONDO:0014775,combined oxidative phosphorylation deficiency 28,COXPD28 - combined oxidative phosphorylation defect type 28 | Neonatal severe cardiopulmonary failure due to mitochondrial methylation defect | Combined oxidative phosphorylation defect type 28 | Combined oxidative phosphorylation defect type 28 (disorder)
+BMGC_DS18775,BMG_DS072087,1187642008,"Macrocephaly, intellectual disability, left ventricular non compaction syndrome",,,,,,,C5569083,,,,,"Macrocephaly, intellectual disability, left ventricular non compaction syndrome (disorder) | Macrocephaly, intellectual disability, left ventricular non compaction syndrome"
+BMGC_DS18776,BMG_DS072088,1187643003,"Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome",,,,,,,C5569084,,616719,MONDO:0014744,acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome,"Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome (disorder) | Autosomal recessive spinocerebellar ataxia type 21 | Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome"
+BMGC_DS18777,BMG_DS072160,128602000,Heterotropia,Strabismus,,,,,,C5574650,D013285,,,,Heterotropia | Heterotropia (disorder)
+BMGC_DS18778,BMG_DS072165,6624005;25569003,Ventricular tachyarrhythmia,,,,,,,C5574657,,,,,Ventricular tachyarrhythmia | Ventricular tachyarrhythmia (disorder) | Ventricular tachycardia | Ventricular tachycardia (disorder) | VT - ventricular tachycardia
+BMGC_DS18779,BMG_DS072166,,,,,,,,,C5574658,,,MONDO:0000389,atelosteogenesis,
+BMGC_DS18780,BMG_DS072167,29914000,Dihydrolipoamide dehydrogenase deficiency (disorder),,,,,,,C5574660,,246900,MONDO:0009529,pyruvate dehydrogenase E3 deficiency,"Dihydrolipoamide dehydrogenase deficiency | Congenital infantile lactic acidosis due to LAD deficiency | Maple syrup urine disease with lactic acidosis | Maple syrup urine disease, type III | Deficiency of diaphorase | Cytochrome-b reductase deficiency | Deficiency of dihydrolipoamide dehydrogenase | Lactic acidosis due to LAD deficiency | DLD - Dihydrolipoamide dehydrogenase deficiency | Deficiency of lipoamide reductase (NADH) | Diaphorase deficiency | Dihydrolipoyl dehydrogenase deficiency | Lipoamide dehydrogenase deficiency | Dihydrolipoamide dehydrogenase deficiency (disorder)"
+BMGC_DS18781,BMG_DS072169,,"Epileptic Encephalopathy, Early Infantile, 3",,,,,,,C5574665,C562695,609304,MONDO:0012245,"developmental and epileptic encephalopathy, 3",
+BMGC_DS18782,BMG_DS072171,,"ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia",,,,,DOID:0111398,congenital dyserythropoietic anemia type Ia,C5574667,,224120;607465,MONDO:0009135,"anemia, congenital dyserythropoietic, type 1a",
+BMGC_DS18783,BMG_DS072172,398148000,Hereditary sensory and autonomic neuropathy type II,,,,,,,C5574675,,,MONDO:0019941,hereditary sensory and autonomic neuropathy type 2,"Hereditary sensory and autonomic neuropathy type II (disorder) | Hereditary sensory and autonomic neuropathy type II | Hereditary sensory and autonomic neuropathy, type II | Painless whitlow disease | Dominant hereditary sensory neuropathy, type II"
+BMGC_DS18784,BMG_DS072173,1197494003,Hyaline fibromatosis syndrome,,,,,,,C5574677,,228600,MONDO:0009229,hyaline fibromatosis syndrome,Hyaline fibromatosis syndrome | Hyaline fibromatosis syndrome (disorder)
+BMGC_DS18785,BMG_DS072174,238867003,Infantile systemic hyalinosis (disorder),,,,,,,C5574678,,236490,MONDO:0016331,infantile systemic hyalinosis,Infantile systemic hyalinosis | Infantile systemic hyalinosis (disorder)
+BMGC_DS18786,BMG_DS072176,,CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2,,,,,DOID:0080207,CAKUT2,C5574705,,143400;604613,MONDO:0027676,congenital anomalies of kidney and urinary tract 2,
+BMGC_DS18787,BMG_DS072177,76376003;198246007;155988000,Adenomyosis,Adenomyosis,,,,,,C5574708,D062788,600458,MONDO:0010888,adenomyosis,Endometriosis of uterus | Endometriosis of uterus (disorder) | Endometriosis (& [adenomyosis]) | Adenomyosis - uterine endomet. | Endometriosis | Adenomyosis | Endometriosis (& [adenomyosis]) (disorder) | Endometriosis (& [adenomyosis]) | Adenomyosis - uterine endomet. | Adenomyosis | Endometriosis | Endometriosis (& [adenomyosis]) (disorder)
+BMGC_DS18788,BMG_DS072179,,"Encephalomyelitis, Allergic","Encephalomyelitis, Autoimmune, Experimental",,,,,,C5574734,D004681,,MONDO:0005134,experimental autoimmune encephalomyelitis,
+BMGC_DS18789,BMG_DS072183,715923003,Lysosomal acid lipase deficiency,,,,,DOID:0080217,lysosomal acid lipase deficiency,C5574740,,,MONDO:0800449,lysosomal acid lipase deficiency,LAL (Lysosomal acid lipase) deficiency | Lysosomal acid lipase deficiency | Lysosomal acid lipase deficiency (disorder) | LALD - Lysosomal acid lipase deficiency
+BMGC_DS18790,BMG_DS072185,13902000;156365002;200938002,Discoid lupus erythematosus,,EB51.Z,"Chronic cutaneous lupus erythematosus, unspecified",L93.0,,,C5574816,,MTHU076645,MONDO:0019558,discoid lupus erythematosus,Discoid lupus erythematosus | Discoid lupus erythematosus (disorder) | Discoid lupus erythematosus | DLE - Discoid lupus erythematosus | LE - Discoid lupus erythematosus | Discoid lupus erythematosus (disorder)
+BMGC_DS18791,BMG_DS072186,128459005;298285004,Systemic sclerosis with limited cutaneous involvement,,,,,,,C5574860,,,,,"Systemic sclerosis, limited | Systemic sclerosis, limited (disorder) | Limited cutaneous systemic sclerosis | Systemic sclerosis with limited cutaneous involvement | Systemic sclerosis with limited cutaneous involvement (disorder) | Acrosclerosis"
+BMGC_DS18792,BMG_DS072188,234143003,Parkes Weber syndrome,,,,,,,C5574870,,,,,Parkes Weber syndrome | Parkes Weber syndrome (disorder)
+BMGC_DS18793,BMG_DS072190,,"PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC",,,,,,,C5574905,,261680;614168,MONDO:0009866,"phosphoenolpyruvate carboxykinase deficiency, cytosolic",
+BMGC_DS18794,BMG_DS072191,,,,,,,,,C5574918,,189800,MONDO:0100467,preeclampsia/eclampsia 1,
+BMGC_DS18795,BMG_DS072192,,,,,,,,,C5574922,,,MONDO:0017990,catecholaminergic polymorphic ventricular tachycardia,
+BMGC_DS18796,BMG_DS072194,699256006,Timothy syndrome type 1,,,,,,,C5574939,,,MONDO:0035678,Timothy syndrome type 1,Long QT syndrome with syndactyly | Timothy syndrome type 1 (disorder) | Timothy syndrome classic type | Timothy syndrome type 1
+BMGC_DS18797,BMG_DS072195,713401006,Combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria,,,,,DOID:0111619,combined D-2- and L-2-hydroxyglutaric aciduria,C5574940,,615182,MONDO:0014072,"D,L-2-hydroxyglutaric aciduria","Combined D-2-hydroxyglutaric acidemia and L-2-hydroxyglutaric acidemia | Combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria (disorder) | Combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria | D,L-2-hydroxyglutaric acidaemia | D,L-2-hydroxyglutaric acidemia | Combined D-2-hydroxyglutaric acidaemia and L-2-hydroxyglutaric acidaemia"
+BMGC_DS18798,BMG_DS072196,,"PAROXYSMAL NONKINESIGENIC DYSKINESIA, 3, WITH OR WITHOUT GENERALIZED EPILEPSY",,,,,DOID:0070442,paroxysmal nonkinesigenic dyskinesia 3,C5574945,,600150;609446,MONDO:0012276,generalized epilepsy-paroxysmal dyskinesia syndrome,
+BMGC_DS18799,BMG_DS072197,,Congenital disorder of glycosylation type II,,,,,DOID:0050571,congenital disorder of glycosylation type II,C5574948,C535747,,MONDO:0005501,congenital disorder of glycosylation type II,
+BMGC_DS18800,BMG_DS072198,,Netherton Syndrome,Netherton Syndrome,,,,,,C5574950,D056770,256500,MONDO:0009735,Netherton syndrome,
+BMGC_DS18801,BMG_DS072200,,"NAIL DISORDER, NONSYNDROMIC CONGENITAL, 7",,,,,DOID:0080085,nonsyndromic congenital nail disorder 7,C5574953,,605779,MONDO:0011595,nonsyndromic congenital nail disorder 7,
+BMGC_DS18802,BMG_DS072202,,HYPOGONADOTROPIC HYPOGONADISM 24 WITH OR WITHOUT ANOSMIA,,,,,,,C5574957,,229070,MONDO:0009239,hypogonadotropic hypogonadism 24 without anosmia,
+BMGC_DS18803,BMG_DS072203,1010609002,Mesomelic dysplasia of upper limb,,,,,,,C5574958,,191440,MONDO:0008620,upper limb mesomelic dysplasia,Mesomelic dysplasia of upper limb (disorder) | Mesomelic dysplasia of upper limb
+BMGC_DS18804,BMG_DS072204,724069009,Patterson Stevenson Fontaine syndrome,,,,,,,C5574964,C536311,183700,MONDO:0008465,Patterson-Stevenson-Fontaine syndrome,Patterson Stevenson Fontaine syndrome (disorder) | Patterson Stevenson Fontaine syndrome | Split foot deformity with mandibulofacial dysostosis syndrome
+BMGC_DS18805,BMG_DS072205,,,,,,,,,C5574965,,136760,MONDO:0007636,frontorhiny,
+BMGC_DS18806,BMG_DS072206,,,,,,,,,C5574973,,,MONDO:0020542,malignant Sertoli-Leydig cell tumor of ovary,
+BMGC_DS18807,BMG_DS072208,,,,,,,,,C5574994,,186000,MONDO:0008513,synpolydactyly type 1,
+BMGC_DS18808,BMG_DS072209,,IMMUNODEFICIENCY 48,,,,,,,C5575025,,269840;176947,MONDO:0010023,combined immunodeficiency due to ZAP70 deficiency,
+BMGC_DS18809,BMG_DS072211,1229946007,MAGEL2-related Prader-Willi-like syndrome,,,,,,,C5575066,,208080;615547,MONDO:0014243,Schaaf-Yang syndrome,MAGE family member L2-related Prader-Willi-like syndrome (disorder) | MAGE family member L2-related Prader-Willi-like syndrome | MAGEL2-related Prader-Willi-like syndrome | Schaaf Yang syndrome
+BMGC_DS18810,BMG_DS072212,1230018005,Corticobasal syndrome,,,,,,,C5575119,,,MONDO:0018696,corticobasal syndrome,Corticobasal syndrome (disorder) | Corticobasal syndrome
+BMGC_DS18811,BMG_DS072213,,"DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES",,,,,,,C5575225,,182790,,,
+BMGC_DS18812,BMG_DS072215,,,,,,,,,C5575231,,,MONDO:0017615,benign familial infantile epilepsy,
+BMGC_DS18813,BMG_DS072216,,,,,,,,,C5575272,,619964,MONDO:0859263,"developmental delay, impaired speech, and behavioral abnormalities, with or without seizures",
+BMGC_DS18814,BMG_DS072219,,"CRANIOTUBULAR DYSPLASIA, IKEGAWA TYPE",,,,,DOID:0112340,craniotubular dysplasia Ikegawa type,C5575335,,619727;619722,MONDO:0859226,"craniotubular dysplasia, Ikegawa type",
+BMGC_DS18815,BMG_DS072222,,,,,,,,,C5575375,,,MONDO:0015244,autosomal recessive cerebellar ataxia,
+BMGC_DS18816,BMG_DS072223,,"AUTOINFLAMMATORY SYNDROME, FAMILIAL, X-LINKED, BEHCET-LIKE 2",,,,,,,C5575495,,300775;301074,MONDO:0024770,"autoinflammatory syndrome, familial, X-linked, Behcet-like 2",
+BMGC_DS18817,BMG_DS072225,1237339005,Severe primary trimethylaminuria,,,,,,,C5575503,,602079,MONDO:0018767,severe primary trimethylaminuria,Severe primary trimethylaminuria (disorder) | Severe primary trimethylaminuria
+BMGC_DS18818,BMG_DS072226,,,,,,,,,C5575558,,,MONDO:0017830,severe Canavan disease,
+BMGC_DS18819,BMG_DS072230,1230376005,Contactin associated protein 2-related developmental and epileptic encephalopathy,,,,,,,C5575702,,,,,"Contactin associated protein 2-related developmental and epileptic encephalopathy | CNTNAP2-related developmental and epileptic encephalopathy | Cortical dysplasia, focal epilepsy syndrome | Contactin associated protein 2-related developmental and epileptic encephalopathy (disorder)"
+BMGC_DS18820,BMG_DS072231,1230097004,Atypical Timothy syndrome,,,,,,,C5575746,,,MONDO:0021172,"Timothy syndrome, atypical type",Atypical long QT syndrome type 8 | Atypical Timothy syndrome (disorder) | Atypical Timothy syndrome | Timothy syndrome atypical type
+BMGC_DS18821,BMG_DS072248,,,,,,,,,C5669918,,,MONDO:0858939,"diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype",
+BMGC_DS18822,BMG_DS072249,,,,,,,,,C5669919,,,MONDO:0858940,infant-type hemispheric glioma,
+BMGC_DS18823,BMG_DS072250,,,,,,,,,C5670122,,,MONDO:0858958,high-grade astrocytoma with piloid features,
+BMGC_DS18824,BMG_DS072257,,,,,,,DOID:0070480,schwannomatosis 1,C5670707,,,,,
+BMGC_DS18825,BMG_DS072258,,,,,,,DOID:0070481,schwannomatosis 2,C5670708,,,,,
+BMGC_DS18826,BMG_DS072263,,Autoimmune Encephalitis,Autoimmune Diseases of the Nervous System,,,,,,C5671289,D020274,,MONDO:0020640,autoimmune encephalitis,
+BMGC_DS18827,BMG_DS072278,,Autosomal dominant limb girdle muscular dystrophy,,,,G71.031,,,C5675009,,,MONDO:0015151,"muscular dystrophy, limb-girdle, autosomal dominant",
+BMGC_DS18828,BMG_DS072459,,"ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IIIa",,,,,,,C5676874,,105600,MONDO:0007109,congenital dyserythropoietic anemia type 3,
+BMGC_DS18829,BMG_DS072460,,"EPIDERMOLYSIS BULLOSA, JUNCTIONAL 5B, WITH PYLORIC ATRESIA",,,,,,,C5676875,,147557;226730,MONDO:0009183,junctional epidermolysis bullosa with pyloric atresia,
+BMGC_DS18830,BMG_DS072461,,CAREY-FINEMAN-ZITER SYNDROME 1,,,,,DOID:0080194,Carey-Fineman-Ziter syndrome,C5676876,,254940,MONDO:0800437,Carey-Fineman-Ziter syndrome 1,
+BMGC_DS18831,BMG_DS072462,,"PULMONARY HYPERTENSION, PRIMARY, 5",,,,,,,C5676877,,265400;610232,MONDO:0009935,"pulmonary hypertension, primary, autosomal recessive",
+BMGC_DS18832,BMG_DS072463,,RESTRICTIVE DERMOPATHY 1,,,,,DOID:0070369,restrictive dermopathy 1,C5676878,,275210;606480,MONDO:0800042,restrictive dermopathy 1,
+BMGC_DS18833,BMG_DS072464,,"THROMBOPHILIA, X-LINKED, DUE TO FACTOR VIII DEFECT",,,,,,,C5676879,,300841;301071,MONDO:0859082,"thrombophilia, X-linked, due to factor 8 defect",
+BMGC_DS18834,BMG_DS072465,,"MYOPATHY, DISTAL, 7, ADULT-ONSET, X-LINKED",,,,,,,C5676880,,300226;301075,MONDO:0024771,"myopathy, distal, 7, adult-onset, X-linked",
+BMGC_DS18835,BMG_DS072466,,,,,,,,,C5676881,,301076,MONDO:0024772,"intellectual developmental disorder, X-linked, syndromic, Pilorge type",
+BMGC_DS18836,BMG_DS072467,,"SPERMATOGENIC FAILURE, X-LINKED, 4",,,,,DOID:0070595,X-linked spermatogenic failure 4,C5676882,,301077;300369,MONDO:0024773,"spermatogenic failure, X-linked, 4",
+BMGC_DS18837,BMG_DS072468,,"IMMUNODEFICIENCY 98 WITH AUTOINFLAMMATION, X-LINKED",,,,,,,C5676883,,301078;300366,MONDO:0024777,"immunodeficiency 98 with autoinflammation, X-linked",
+BMGC_DS18838,BMG_DS072469,,SYSTEMIC LUPUS ERYTHEMATOSUS 17,,,,,,,C5676884,,300365;301080,MONDO:0859083,systemic lupus erythematosus 17,
+BMGC_DS18839,BMG_DS072470,,"AUTOINFLAMMATORY DISEASE, SYSTEMIC, X-LINKED",,,,,,,C5676885,,300248;301081,MONDO:0800129,"autoinflammatory disease, X-linked",
+BMGC_DS18840,BMG_DS072471,,IMMUNODEFICIENCY 102,,,,,,,C5676886,,300441;301082,MONDO:0024781,immunodeficiency 102,
+BMGC_DS18841,BMG_DS072472,,STUVE-WIEDEMANN SYNDROME 1,,,,,,,C5676888,,151443;601559,MONDO:0800043,Stüve-Wiedemann syndrome 1,
+BMGC_DS18842,BMG_DS072473,,"RETINITIS PIGMENTOSA 94, VARIABLE AGE AT ONSET",,,,,,,C5676889,,609868;604232,MONDO:0800328,"retinitis pigmentosa 94, variable age at onset",
+BMGC_DS18843,BMG_DS072474,,IMMUNODEFICIENCY 104,,,,,,,C5676890,,146661;608971,MONDO:0012163,immunodeficiency 104,
+BMGC_DS18844,BMG_DS072475,,,,,,,,,C5676891,,609698,MONDO:0800046,"thyroid hormone metabolism, abnormal 1",
+BMGC_DS18845,BMG_DS072476,,"MACROTHROMBOCYTOPENIA, ISOLATED, 1, AUTOSOMAL DOMINANT",,,,,,,C5676892,,612901;613112,MONDO:0800047,"macrothrombocytopenia, isolated, 1, autosomal dominant",
+BMGC_DS18846,BMG_DS072477,,"3-METHYLGLUTACONIC ACIDURIA, TYPE VIIB",,,,,DOID:0081134;DOID:0110003,"3-methylglutaconic aciduria type 7b | 3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia",C5676893,,616271,MONDO:0014561,"3-methylglutaconic aciduria, type VIIB",
+BMGC_DS18847,BMG_DS072478,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, IMPAIRED LANGUAGE, AND DYSMORPHIC FEATURES",,,,,DOID:0070070,autosomal dominant intellectual developmental disorder 40,C5676894,,616327;616579,MONDO:0014699,"intellectual disability, autosomal dominant 40",
+BMGC_DS18848,BMG_DS072479,,"CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 2",,,,,DOID:0081125,"craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2",C5676895,,616994;619960,MONDO:0859567,"craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2",
+BMGC_DS18849,BMG_DS072480,,,,,,,,,C5676896,,617863,MONDO:0029465,"intellectual developmental disorder, autosomal dominant 69",
+BMGC_DS18850,BMG_DS072481,,KNOBLOCH SYNDROME 2,,,,,,,C5676897,,605022;618458,MONDO:0100119,Knobloch syndrome 2,
+BMGC_DS18851,BMG_DS072482,,,,,,,,,C5676898,,619702,MONDO:0859222,"heterotaxy, visceral, 12, autosomal",
+BMGC_DS18852,BMG_DS072483,,IMMUNODEFICIENCY 93 AND HYPERTROPHIC CARDIOMYOPATHY,,,,,,,C5676899,,610594;619705,MONDO:0030528,immunodeficiency 93 and hypertrophic cardiomyopathy,
+BMGC_DS18853,BMG_DS072484,,"AGAMMAGLOBULINEMIA 10, AUTOSOMAL DOMINANT",,,,,DOID:0081142,agammaglobulinemia 10,C5676900,,165170;619707,MONDO:0030529,"agammaglobulinemia 10, autosomal dominant",
+BMGC_DS18854,BMG_DS072485,,GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME 2,,,,,,,C5676901,,600286;619708,MONDO:0030669,gastrointestinal defects and immunodeficiency syndrome 2,
+BMGC_DS18855,BMG_DS072486,,,,,,,,,C5676902,,619717,MONDO:0030533,"intellectual developmental disorder, autosomal recessive 73",
+BMGC_DS18856,BMG_DS072487,,HYPOGONADOTROPIC HYPOGONADISM 26 WITH OR WITHOUT ANOSMIA,,,,,,,C5676903,,619718,MONDO:0030534,hypogonadotropic hypogonadism 26 with or without anosmia,
+BMGC_DS18857,BMG_DS072488,,INTELLECTUAL DISABILITY AND MYOPATHY SYNDROME,,,,,DOID:0070600,intellectual disability and myopathy syndrome,C5676904,,601439;619719,MONDO:0859224,intellectual disability and myopathy syndrome,
+BMGC_DS18858,BMG_DS072489,,BRYANT-LI-BHOJ NEURODEVELOPMENTAL SYNDROME 1,,,,,DOID:0051011,Bryant-Li-Bhoj neurodevelopmental syndrome 1,C5676905,,601128;619720,MONDO:0030606,Bryant-Li-Bhoj neurodevelopmental syndrome 1,
+BMGC_DS18859,BMG_DS072490,,BRYANT-LI-BHOJ NEURODEVELOPMENTAL SYNDROME 2,,,,,DOID:0051012,Bryant-Li-Bhoj neurodevelopmental syndrome 2,C5676906,,619721;601058,MONDO:0030607,Bryant-Li-Bhoj neurodevelopmental syndrome 2,
+BMGC_DS18860,BMG_DS072491,,"DYSTONIA 34, MYOCLONIC",,,,,DOID:0060957,myoclonic dystonia 34,C5676907,,619724;605879,MONDO:0030538,"dystonia 34, myoclonic",
+BMGC_DS18861,BMG_DS072492,,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT VARIABLE MOVEMENT OR BEHAVIORAL ABNORMALITIES,,,,,,,C5676908,,605879;619725,MONDO:0859225,neurodevelopmental disorder with or without variable movement or behavioral abnormalities,
+BMGC_DS18862,BMG_DS072493,,INCLUSION BODY MYOPATHY AND BRAIN WHITE MATTER ABNORMALITIES,,,,,DOID:0081121,inclusion body myopathy and brain white matter abnormalities,C5676909,,602572;619733,MONDO:0850514,inclusion body myopathy and brain white matter abnormalities,
+BMGC_DS18863,BMG_DS072494,,"SPASTIC PARAPLEGIA 86, AUTOSOMAL RECESSIVE",,,,,DOID:0112342,hereditary spastic paraplegia 86,C5676910,,142620;619735,MONDO:0030673,"spastic paraplegia 86, autosomal recessive",
+BMGC_DS18864,BMG_DS072495,,TEEBI HYPERTELORISM SYNDROME 2,,,,,DOID:0081074,Teebi hypertelorism syndrome 2,C5676911,,619736;600023,MONDO:0030674,Teebi hypertelorism syndrome 2,
+BMGC_DS18865,BMG_DS072496,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 54,,,,,DOID:0070427,combined oxidative phosphorylation deficiency 54,C5676912,,609947;619737,MONDO:0030543,combined oxidative phosphorylation deficiency 54,
+BMGC_DS18866,BMG_DS072497,,"PARKINSONISM-DYSTONIA 3, CHILDHOOD-ONSET",,,,,,,C5676913,,604733;619738,MONDO:0030676,"parkinsonism-dystonia 3, childhood-onset",
+BMGC_DS18867,BMG_DS072498,,"CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1I",,,,,,,C5676914,,619742;614366,MONDO:0030677,"Charcot-Marie-Tooth disease, demyelinating, IIA 1I",
+BMGC_DS18868,BMG_DS072499,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 55,,,,,DOID:0070428,combined oxidative phosphorylation deficiency 55,C5676915,,619743;601778,MONDO:0859228,combined oxidative phosphorylation deficiency 55,
+BMGC_DS18869,BMG_DS072500,,NOONAN SYNDROME 14,,,,,,,C5676916,,609292;619745,MONDO:0030679,Noonan syndrome 14,
+BMGC_DS18870,BMG_DS072501,,"CARDIOMYOPATHY, DILATED, 2F",,,,,DOID:0081162,dilated cardiomyopathy 2F,C5676917,,603885;619747,MONDO:0030680,"cardiomyopathy, dilated, 2F",
+BMGC_DS18871,BMG_DS072502,,IMMUNODEFICIENCY 94 WITH AUTOINFLAMMATION AND DYSMORPHIC FACIES,,,,,,,C5676918,,600694;619750,MONDO:0030681,immunodeficiency 94 with autoinflammation and dysmorphic facies,
+BMGC_DS18872,BMG_DS072503,,STUVE-WIEDEMANN SYNDROME 2,,,,,,,C5676919,,600694;619751,MONDO:0030756,Stuve-Wiedemann syndrome 2,
+BMGC_DS18873,BMG_DS072504,,"HYPER-IgE SYNDROME 4A, AUTOSOMAL DOMINANT, WITH RECURRENT INFECTIONS",,,,,,,C5676920,,600694;619752,MONDO:0800131,"hyper-IgE recurrent infection syndrome 4A, autosomal dominant",
+BMGC_DS18874,BMG_DS072505,,HYPOGONADOTROPIC HYPOGONADISM 27 WITHOUT ANOSMIA,,,,,,,C5676921,,162361;619755,MONDO:0030684,hypogonadotropic hypogonadism 27 without anosmia,
+BMGC_DS18875,BMG_DS072506,,TESSADORI-BICKNELL-VAN HAAFTEN NEURODEVELOPMENTAL SYNDROME 1,,,,,,,C5676922,,602827;619758,MONDO:0030729,Tessadori-van Haaften neurodevelopmental syndrome 1,
+BMGC_DS18876,BMG_DS072507,,TESSADORI-BICKNELL-VAN HAAFTEN NEURODEVELOPMENTAL SYNDROME 2,,,,,,,C5676923,,602826;619759,MONDO:0030730,Tessadori-van Haaften neurodevelopmental syndrome 2,
+BMGC_DS18877,BMG_DS072508,,"CEREBELLAR DYSFUNCTION, IMPAIRED INTELLECTUAL DEVELOPMENT, AND HYPOGONADOTROPIC HYPOGONADISM",,,,,,,C5676924,,619761;616741,MONDO:0859229,"cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism",
+BMGC_DS18878,BMG_DS072509,,KURY-ISIDOR SYNDROME,,,,,,,C5676925,,603089;619762,MONDO:0859230,Kury-Isidor syndrome,
+BMGC_DS18879,BMG_DS072510,,"CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1H",,,,,,,C5676926,,604580;619764,MONDO:0030689,"Charcot-Marie-Tooth disease, demyelinating, IIA 1H",
+BMGC_DS18880,BMG_DS072511,,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 6",,,,,,,C5676927,,179835;619767,MONDO:0030690,"pulmonary fibrosis and/or bone marrow failure, telomere-related, 6",
+BMGC_DS18881,BMG_DS072512,,"MACROCEPHALY, NEURODEVELOPMENTAL DELAY, LYMPHOID HYPERPLASIA, AND PERSISTENT FETAL HEMOGLOBIN",,,,,,,C5676928,,619769;605878,MONDO:0859231,"macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin",
+BMGC_DS18882,BMG_DS072513,,IMMUNODEFICIENCY 95,,,,,,,C5676929,,606951;619773,MONDO:0030692,immunodeficiency 95,
+BMGC_DS18883,BMG_DS072514,,IMMUNODEFICIENCY 96,,,,,,,C5676930,,126391;619774,MONDO:0030693,immunodeficiency 96,
+BMGC_DS18884,BMG_DS072515,,CONGENITAL DISORDER OF DEGLYCOSYLATION 2,,,,,DOID:0060990,congenital disorder of deglycosylation 2,C5676931,,619775;154580,MONDO:0030770,congenital disorder of deglycosylation 2,
+BMGC_DS18885,BMG_DS072516,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 100,,,,,DOID:0070386,developmental and epileptic encephalopathy 100,C5676932,,619777;609100,MONDO:0030695,developmental and epileptic encephalopathy 100,
+BMGC_DS18886,BMG_DS072517,,MITOCHONDRIAL DNA DEPLETION SYNDROME 20 (MNGIE TYPE),,,,,DOID:0070451,mitochondrial DNA depletion syndrome 20,C5676934,,600940;619780,MONDO:0030696,mitochondrial DNA depletion syndrome 20 (mngie type),
+BMGC_DS18887,BMG_DS072518,,"MYOPIA 28, AUTOSOMAL RECESSIVE",,,,,,,C5676935,,607163;619781,MONDO:0030697,"myopia 28, autosomal recessive",
+BMGC_DS18888,BMG_DS072519,,"EPIDERMOLYSIS BULLOSA, JUNCTIONAL 2A, INTERMEDIATE",,,,,,,C5676936,,600805;619783,MONDO:0030746,"epidermolysis bullosa, junctional 2A, intermediate",
+BMGC_DS18889,BMG_DS072520,,"EPIDERMOLYSIS BULLOSA, JUNCTIONAL 2B, SEVERE",,,,,,,C5676937,,619784;600805,MONDO:0030747,"epidermolysis bullosa, junctional 2B, severe",
+BMGC_DS18890,BMG_DS072521,,"EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3A, INTERMEDIATE",,,,,,,C5676938,,150292;619785,MONDO:0030748,"epidermolysis bullosa, junctional 3A, intermediate",
+BMGC_DS18891,BMG_DS072522,,"EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3B, SEVERE",,,,,,,C5676939,,150292;619786,MONDO:0030749,"epidermolysis bullosa, junctional 3B, severe",
+BMGC_DS18892,BMG_DS072523,,"ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IIIb, AUTOSOMAL RECESSIVE",,,,,DOID:0051001,congenital dyserythropoietic anemia type IIIb,C5676940,,619789,MONDO:0030711,"Anemia, congenital dyserythropoietic, type IIIb, autosomal recessive",
+BMGC_DS18893,BMG_DS072524,,OCULOPHARYNGODISTAL MYOPATHY 4,,,,,DOID:0081300,oculopharyngodistal myopathy 4,C5676941,,614092;619790,MONDO:0030712,oculopharyngodistal myopathy 4,
+BMGC_DS18894,BMG_DS072525,,RESTRICTIVE DERMOPATHY 2,,,,,DOID:0070370,restrictive dermopathy 2,C5676942,,619793;150330,MONDO:0030781,restrictive dermopathy 2,
+BMGC_DS18895,BMG_DS072526,,"OSTEOGENESIS IMPERFECTA, TYPE XXII",,,,,,,C5676943,,619795;618788,MONDO:0030714,"osteogenesis imperfecta, IIA 22",
+BMGC_DS18896,BMG_DS072527,,NEURODEVELOPMENTAL DISORDER WITH CENTRAL HYPOTONIA AND DYSMORPHIC FACIES,,,,,,,C5676944,,619797;605314,MONDO:0859232,neurodevelopmental disorder with central hypotonia and dysmorphic facies,
+BMGC_DS18897,BMG_DS072528,,SPERMATOGENIC FAILURE 66,,,,,DOID:0070565,spermatogenic failure 66,C5676945,,608498;619799,MONDO:0030716,spermatogenic failure 66,
+BMGC_DS18898,BMG_DS072529,,IMMUNODEFICIENCY 97 WITH AUTOINFLAMMATION,,,,,,,C5676946,,601232;619802,MONDO:0030717,immunodeficiency 97 with autoinflammation,
+BMGC_DS18899,BMG_DS072530,,SPERMATOGENIC FAILURE 67,,,,,DOID:0070566,spermatogenic failure 67,C5676947,,613481;619803,MONDO:0030718,spermatogenic failure 67,
+BMGC_DS18900,BMG_DS072531,,"DEAFNESS, AUTOSOMAL DOMINANT 82",,,,,DOID:0070603,autosomal dominant nonsyndromic deafness 82,C5676948,,619804;108733,MONDO:0030719,"hearing loss, autosomal dominant 82",
+BMGC_DS18901,BMG_DS072532,,SPERMATOGENIC FAILURE 68,,,,,DOID:0070567,spermatogenic failure 68,C5676949,,619776;619805,MONDO:0030721,spermatogenic failure 68,
+BMGC_DS18902,BMG_DS072533,,SPINOCEREBELLAR ATAXIA 49,,,,,,,C5676950,,611170;619806,MONDO:0030805,spinocerebellar ataxia 49,
+BMGC_DS18903,BMG_DS072534,,"DEAFNESS, AUTOSOMAL DOMINANT 83",,,,,DOID:0070609,autosomal dominant nonsyndromic deafness 83,C5676951,,157129;619808,MONDO:0030723,"hearing loss, autosomal dominant 83",
+BMGC_DS18904,BMG_DS072535,,"DEAFNESS, AUTOSOMAL DOMINANT 84",,,,,DOID:0070604,autosomal dominant nonsyndromic deafness 84,C5676952,,619810;605868,MONDO:0030724,"hearing loss, autosomal dominant 84",
+BMGC_DS18905,BMG_DS072536,,"NEUTROPENIA, SEVERE CONGENITAL, 9, AUTOSOMAL DOMINANT",,,,,,,C5676954,,616254;619813,MONDO:0030726,"neutropenia, severe congenital, 9, autosomal dominant",
+BMGC_DS18906,BMG_DS072537,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 101,,,,,DOID:0070387,developmental and epileptic encephalopathy 101,C5676955,,138249;619814,MONDO:0030727,developmental and epileptic encephalopathy 101,
+BMGC_DS18907,BMG_DS072538,,"EPIDERMOLYSIS BULLOSA, JUNCTIONAL 5A, INTERMEDIATE",,,,,,,C5676956,,147557;619816,MONDO:0030768,"epidermolysis bullosa, junctional 5A, intermediate",
+BMGC_DS18908,BMG_DS072539,,"EPIDERMOLYSIS BULLOSA, JUNCTIONAL 6, WITH PYLORIC ATRESIA",,,,,,,C5676957,,619817;147556,MONDO:0859233,"epidermolysis bullosa, junctional 6, with pyloric atresia",
+BMGC_DS18909,BMG_DS072540,,"AGAMMAGLOBULINEMIA 8B, AUTOSOMAL RECESSIVE",,,,,DOID:0081143,agammaglobulinemia 8B,C5676958,,147141;619824,MONDO:0859234,"agammaglobulinemia 8b, autosomal recessive",
+BMGC_DS18910,BMG_DS072541,,"AORTIC ANEURYSM, FAMILIAL THORACIC 12",,,,,,,C5676959,,614476;619825,MONDO:0030731,"aortic aneurysm, familial thoracic 12",
+BMGC_DS18911,BMG_DS072542,,SPERMATOGENIC FAILURE 69,,,,,DOID:0070568,spermatogenic failure 69,C5676960,,619826;609966,MONDO:0030732,spermatogenic failure 69,
+BMGC_DS18912,BMG_DS072543,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 75, WITH NEUROPSYCHIATRIC FEATURES AND VARIANT LISSENCEPHALY",,,,,DOID:0081234,autosomal recessive intellectual developmental disorder 75,C5676961,,619827;605247,MONDO:0030785,"intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly",
+BMGC_DS18913,BMG_DS072544,,SPERMATOGENIC FAILURE 70,,,,,DOID:0070569,spermatogenic failure 70,C5676962,,179061;619828,MONDO:0030733,spermatogenic failure 70,
+BMGC_DS18914,BMG_DS072545,,SPERMATOGENIC FAILURE 71,,,,,DOID:0070570,spermatogenic failure 71,C5676963,,614535;619831,MONDO:0030787,spermatogenic failure 71,
+BMGC_DS18915,BMG_DS072546,,"AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT 3",,,,,DOID:0112373,autosomal dominant auditory neuropathy 3,C5676964,,619832;612048,MONDO:0859235,"auditory neuropathy, autosomal dominant 3",
+BMGC_DS18916,BMG_DS072547,,NEURODEVELOPMENTAL DISORDER WITH NEUROMUSCULAR AND SKELETAL ABNORMALITIES,,,,,,,C5676965,,601581;619833,MONDO:0859236,neurodevelopmental disorder with neuromuscular and skeletal abnormalities,
+BMGC_DS18917,BMG_DS072548,,OVARIAN DYSGENESIS 10,,,,,DOID:0061014,ovarian dysgenesis 10,C5676966,,614535;619834,MONDO:0030736,ovarian dysgenesis 10,
+BMGC_DS18918,BMG_DS072549,,"3-METHYLGLUTACONIC ACIDURIA, TYPE VIIA",,,,,DOID:0081133,3-methylglutaconic aciduria type 7a,C5676967,,619835,MONDO:0859237,"3-methylglutaconic aciduria, type VIIA",
+BMGC_DS18919,BMG_DS072550,,"MACROTHROMBOCYTOPENIA, ISOLATED, 2, AUTOSOMAL DOMINANT",,,,,DOID:0060995,autosomal dominant isolated macrothrombocytopenia 2,C5676968,,605742;619840,MONDO:0030827,"macrothrombocytopenia, isolated, 2, autosomal dominant",
+BMGC_DS18920,BMG_DS072551,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT PERIPHERAL NEUROPATHY,,,,,,,C5676969,,619844,MONDO:0859240,intellectual developmental disorder with or without peripheral neuropathy,
+BMGC_DS18921,BMG_DS072552,,RETINITIS PIGMENTOSA 93,,,,,,,C5676970,,619845;612013,MONDO:0030797,retinitis pigmentosa 93,
+BMGC_DS18922,BMG_DS072553,,IMMUNODEFICIENCY 99 WITH HYPOGAMMAGLOBULINEMIA AND AUTOIMMUNE CYTOPENIAS,,,,,,,C5676971,,611537;619846,MONDO:0030798,immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias,
+BMGC_DS18923,BMG_DS072554,,"NEURODEGENERATION, CHILDHOOD-ONSET, WITH PROGRESSIVE MICROCEPHALY",,,,,,,C5676972,,188345;619847,MONDO:0859241,"neurodegeneration, childhood-onset, with progressive microcephaly",
+BMGC_DS18924,BMG_DS072555,,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 9",,,,,,,C5676973,,619635;619849,MONDO:0030800,"cholestasis, progressive familial intrahepatic, 9",
+BMGC_DS18925,BMG_DS072556,,"LEUKODYSTROPHY, HYPOMYELINATING, 24",,,,,DOID:0070406,hypomyelinating leukodystrophy 24,C5676974,,619851,MONDO:0859242,"leukodystrophy, hypomyelinating, 24",
+BMGC_DS18926,BMG_DS072557,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES",,,,,,,C5676975,,619854;139310,MONDO:0859243,"neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities",
+BMGC_DS18927,BMG_DS072558,,,,,,,,,C5676976,,619855,MONDO:0030839,"thyroid hormone metabolism, abnormal, 2",
+BMGC_DS18928,BMG_DS072559,,AUTOINFLAMMATORY-PANCYTOPENIA SYNDROME,,,,,,,C5676977,,126350;619858,MONDO:0800132,autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency,
+BMGC_DS18929,BMG_DS072560,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 32",,,,,DOID:0070413,autosomal recessive spinocerebellar ataxia 32,C5676978,,604769;619862,MONDO:0859245,"spinocerebellar ataxia, autosomal recessive 32",
+BMGC_DS18930,BMG_DS072561,,"LEUKODYSTROPHY, CHILDHOOD-ONSET, REMITTING",,,,,,,C5676979,,619864;603027,MONDO:0859246,"leukodystrophy, childhood-onset, remitting",
+BMGC_DS18931,BMG_DS072562,,SPERMATOGENIC FAILURE 72,,,,,DOID:0070571,spermatogenic failure 72,C5676980,,619867;608151,MONDO:0030809,spermatogenic failure 72,
+BMGC_DS18932,BMG_DS072563,,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 10",,,,,,,C5676981,,619868;606540,MONDO:0030810,"cholestasis, progressive familial intrahepatic, 10",
+BMGC_DS18933,BMG_DS072564,,"CORNEAL DYSTROPHY, PUNCTIFORM AND POLYCHROMATIC PRE-DESCEMET",,,,,,,C5676982,,604769;619871,MONDO:0859248,"corneal dystrophy, punctiform and polychromatic pre-descemet",
+BMGC_DS18934,BMG_DS072565,,IMMUNODEFICIENCY 101 (VARICELLA ZOSTER VIRUS-SPECIFIC),,,,,,,C5676983,,617455;619872,MONDO:0030813,immunodeficiency 101 (varicella zoster virus-specific),
+BMGC_DS18935,BMG_DS072566,,PARENTI-MIGNOT NEURODEVELOPMENTAL SYNDROME,,,,,,,C5676984,,610771;619873,MONDO:0859249,parenti-mignot neurodevelopmental syndrome,
+BMGC_DS18936,BMG_DS072567,,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 11",,,,,,,C5676985,,607961;619874,MONDO:0030815,"cholestasis, progressive familial intrahepatic, 11",
+BMGC_DS18937,BMG_DS072568,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, NYSTAGMUS, AND SEIZURES",,,,,,,C5676986,,619876;606029,MONDO:0859250,"neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures",
+BMGC_DS18938,BMG_DS072569,,DENTICI-NOVELLI NEURODEVELOPMENTAL SYNDROME,,,,,,,C5676987,,614387;619877,MONDO:0859251,Dentici-Novelli neurodevelopmental syndrome,
+BMGC_DS18939,BMG_DS072570,,SPERMATOGENIC FAILURE 73,,,,,DOID:0070572,spermatogenic failure 73,C5676988,,605794;619878,MONDO:0030818,spermatogenic failure 73,
+BMGC_DS18940,BMG_DS072571,,MECKEL SYNDROME 14,,,,,,,C5676989,,617778;619879,MONDO:0030819,meckel syndrome 14,
+BMGC_DS18941,BMG_DS072572,,NEURODEVELOPMENTAL DISORDER WITH POOR GROWTH AND SKELETAL ANOMALIES,,,,,,,C5676990,,619880;606305,MONDO:0859252,neurodevelopmental disorder with poor growth and skeletal anomalies,
+BMGC_DS18942,BMG_DS072573,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 102,,,,,DOID:0070388,developmental and epileptic encephalopathy 102,C5676991,,619881;604437,MONDO:0030881,developmental and epileptic encephalopathy 102,
+BMGC_DS18943,BMG_DS072574,,"OSTEOPOROSIS, CHILDHOOD- OR JUVENILE-ONSET, WITH DEVELOPMENTAL DELAY",,,,,,,C5676992,,606990;619884,MONDO:0859253,"osteoporosis, childhood- or juvenile-onset, with developmental delay",
+BMGC_DS18944,BMG_DS072575,,RENAL HYPODYSPLASIA/APLASIA 4,,,,,,,C5676993,,601496;619887,MONDO:0030822,renal hypodysplasia/aplasia 4,
+BMGC_DS18945,BMG_DS072576,,HOLOPROSENCEPHALY 14,,,,,,,C5676994,,612835;619895,MONDO:0030886,holoprosencephaly 14,
+BMGC_DS18946,BMG_DS072577,,"CARDIOMYOPATHY, DILATED, 2G",,,,,DOID:0081163,dilated cardiomyopathy 2G,C5676995,,619897;608006,MONDO:0030887,"cardiomyopathy, dilated, 2G",
+BMGC_DS18947,BMG_DS072578,,HEPATORENOCARDIAC DEGENERATIVE FIBROSIS,,,,,,,C5676996,,604730;619902,MONDO:0859254,hepatorenocardiac degenerative fibrosis,
+BMGC_DS18948,BMG_DS072579,,"PERIPHERAL MOTOR NEUROPATHY, CHILDHOOD-ONSET, BIOTIN-RESPONSIVE",,,,,,,C5676997,,604024;619903,MONDO:0859255,"peripheral motor neuropathy, childhood-onset, biotin-responsive",
+BMGC_DS18949,BMG_DS072580,,NEURODEVELOPMENTAL DISORDER WITH LANGUAGE DELAY AND SEIZURES,,,,,DOID:0070444,neurodevelopmental disorder with language delay and seizures,C5676998,,619908;600687,MONDO:0859256,neurodevelopmental disorder with language delay and seizures,
+BMGC_DS18950,BMG_DS072581,,"PONTOCEREBELLAR HYPOPLASIA, TYPE 17",,,,,,,C5676999,,619909;616741,MONDO:0030890,"pontocerebellar hypoplasia, IIA 17",
+BMGC_DS18951,BMG_DS072582,,,,,,,,,C5677000,,619910,MONDO:0030891,"intellectual developmental disorder, autosomal dominant 66",
+BMGC_DS18952,BMG_DS072583,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND EARLY-ONSET DOPA-RESPONSIVE DYSTONIA-PARKINSONISM,,,,,,,C5677001,,601828;619911,MONDO:0859257,intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism,
+BMGC_DS18953,BMG_DS072584,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 103,,,,,DOID:0070389,developmental and epileptic encephalopathy 103,C5677002,,176256;619913,MONDO:0030957,developmental and epileptic encephalopathy 103,
+BMGC_DS18954,BMG_DS072585,,"DYSTONIA 35, CHILDHOOD-ONSET",,,,,DOID:0060955,"dystonia 35, childhood-onset",C5677003,,613663;619921,MONDO:0030958,"dystonia 35, childhood-onset",
+BMGC_DS18955,BMG_DS072586,,NEURODEVELOPMENTAL DISORDER WITH DYSTONIA AND SEIZURES,,,,,,,C5677004,,619922;613663,MONDO:0859258,neurodevelopmental disorder with dystonia and seizures,
+BMGC_DS18956,BMG_DS072587,,IMMUNODEFICIENCY 105,,,,,,,C5677005,,151460;619924,MONDO:0800104,immunodeficiency 105,
+BMGC_DS18957,BMG_DS072588,,,,,,,,,C5677006,,619927,MONDO:0030964,"intellectual developmental disorder, autosomal dominant 67",
+BMGC_DS18958,BMG_DS072589,,,,,,,,,C5677007,,619931,MONDO:0030968,"intellectual developmental disorder, autosomal recessive 76",
+BMGC_DS18959,BMG_DS072590,,,,,,,,,C5677008,,619934,MONDO:0030969,"intellectual developmental disorder, autosomal dominant 68",
+BMGC_DS18960,BMG_DS072591,,"IMMUNODEFICIENCY 106, SUSCEPTIBILITY TO VIRAL INFECTIONS",,,,,,,C5677009,,107450;619935,MONDO:0030970,"immunodeficiency 106, susceptibility to viral infections",
+BMGC_DS18961,BMG_DS072592,,SPERMATOGENIC FAILURE 74,,,,,DOID:0070573,spermatogenic failure 74,C5677010,,603382;619937,MONDO:0030972,spermatogenic failure 74,
+BMGC_DS18962,BMG_DS072593,,PREMATURE OVARIAN FAILURE 20,,,,,,,C5677011,,619938;602105,MONDO:0030975,premature ovarian failure 20,
+BMGC_DS18963,BMG_DS072594,,CAREY-FINEMAN-ZITER SYNDROME 2,,,,,,,C5677012,,619912;619941,MONDO:0100292,Carey-Fineman-Ziter syndrome 2,
+BMGC_DS18964,BMG_DS072595,,"WAARDENBURG SYNDROME, TYPE 2F",,,,,,,C5677013,,184745;619947,MONDO:0030983,"Waardenburg syndrome, IIa 2F",
+BMGC_DS18965,BMG_DS072596,,SPERMATOGENIC FAILURE 75,,,,,DOID:0070574,spermatogenic failure 75,C5677014,,618038;619949,MONDO:0030984,spermatogenic failure 75,
+BMGC_DS18966,BMG_DS072598,,TESSADORI-BICKNELL-VAN HAAFTEN NEURODEVELOPMENTAL SYNDROME 4,,,,,,,C5677016,,619951;602833,MONDO:0031000,Tessadori-Van Haaften neurodevelopmental syndrome 4,
+BMGC_DS18967,BMG_DS072599,,DWORSCHAK-PUNETHA NEURODEVELOPMENTAL SYNDROME,,,,,,,C5677017,,601055;619955,MONDO:0859260,Dworschak-Punetha neurodevelopmental syndrome,
+BMGC_DS18968,BMG_DS072600,,,,,,,,,C5677018,,619957,MONDO:0859261,attention deficit-hyperactivity disorder 8,
+BMGC_DS18969,BMG_DS072601,,ACCES SYNDROME,,,,,,,C5677019,,613295;619959,MONDO:0859262,ACCES syndrome,
+BMGC_DS18970,BMG_DS072602,,NEUROCARDIOFACIODIGITAL SYNDROME,,,,,,,C5677020,,606723;619869,MONDO:0859247,neurocardiofaciodigital syndrome,
+BMGC_DS18971,BMG_DS072603,,"CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 1",,,,,DOID:0081124,"craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1",C5677021,,614123;213980,MONDO:0800436,"craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1",
+BMGC_DS18972,BMG_DS072604,,CHILTON-OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME,,,,,,,C5677022,,619841;614062,MONDO:0859239,Chilton-Okur-Chung neurodevelopmental syndrome,
+BMGC_DS18973,BMG_DS072605,,CHROMOSOME 2q23.1 DUPLICATION SYNDROME,,,,,DOID:0070031,autosomal dominant intellectual developmental disorder 1,C5677023,,156200,,,
+BMGC_DS18974,BMG_DS072606,,CHROMOSOME Xq25 TRIPLICATION SYNDROME,,,,,,,C5677024,,300979,,,
+BMGC_DS18975,BMG_DS072607,,DIFFUSE GASTRIC AND LOBULAR BREAST CANCER SYNDROME WITH CLEFT LIP AND WITH OR WITHOUT CLEFT PALATE,,,,,DOID:0080764,hereditary diffuse gastric cancer,C5677027,,137215;192090,,,
+BMGC_DS18976,BMG_DS072608,,"HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2, INTERMEDIATE",,,,,,,C5677030,,107680;619836,MONDO:0859238,"hypoalphalipoproteinemia, primary, 2, intermediate",
+BMGC_DS18977,BMG_DS072619,,"ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IIIb",,,,,,,C5677049,,604980,,,
+BMGC_DS18978,BMG_DS072625,,CUBITUS VALGUS WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND UNUSUAL FACIES,,,,,,,C5677056,,300471,MONDO:0010332,X-linked intellectual disability-cubitus valgus-dysmorphism syndrome,
+BMGC_DS18979,BMG_DS072626,,CHROMOSOME Xq13 DUPLICATION SYNDROME,,,,,,,C5677057,,301069,MONDO:0859081,chromosome Xq13 duplication syndrome,
+BMGC_DS18980,BMG_DS072629,,,,,,,,,C5679572,,,MONDO:0000050,isolated congenital growth hormone deficiency,
+BMGC_DS18981,BMG_DS072630,1336091009,Mild hereditary factor IX deficiency disease,,,,,,,C5679574,,,MONDO:0015717,mild hemophilia B,Mild hereditary factor IX deficiency disease | Mild hemophilia B | Mild haemophilia B | Mild hereditary factor IX deficiency disease (disorder)
+BMGC_DS18982,BMG_DS072631,1336092002,Moderate hereditary factor IX deficiency disease,,,,,,,C5679575,,,MONDO:0015716,moderately severe hemophilia B,Moderate hereditary factor IX deficiency disease (disorder) | Moderate hereditary factor IX deficiency disease | Moderate haemophilia B | Moderate hemophilia B
+BMGC_DS18983,BMG_DS072632,1336093007,Severe hereditary factor IX deficiency disease,,,,,,,C5679576,,,MONDO:0015715,severe hemophilia B,Severe hereditary factor IX deficiency disease | Severe hereditary factor IX deficiency disease (disorder) | Severe hemophilia B | Severe haemophilia B
+BMGC_DS18984,BMG_DS072633,,,,,,,,,C5679577,,,MONDO:0015701,T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency,
+BMGC_DS18985,BMG_DS072634,,,,,,,,,C5679578,,,MONDO:0015703,T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta,
+BMGC_DS18986,BMG_DS072635,,,,,,,,,C5679579,,,MONDO:0015702,T-B+ severe combined immunodeficiency due to CD45 deficiency,
+BMGC_DS18987,BMG_DS072638,,,,,,,,,C5679591,,,MONDO:0015746,male infertility due to globozoospermia,
+BMGC_DS18988,BMG_DS072642,,,,,,,,,C5679612,,,MONDO:0015369,Joubert syndrome and related disorders,
+BMGC_DS18989,BMG_DS072643,1234906009,"46,XX ovotesticular disorder of sex development",,,,,,,C5679613,,,MONDO:0016281,"46,XX ovotesticular disorder of sex development","46,XX ovotesticular disorder of sex development (disorder) | 46,XX ovotesticular disorder of sex development"
+BMGC_DS18990,BMG_DS072644,,,,,,,,,C5679614,,,MONDO:0016614,autosomal recessive ataxia due to PEX10 deficiency,
+BMGC_DS18991,BMG_DS072645,,,,,,,,,C5679615,,,MONDO:0016613,APC-related attenuated familial adenomatous polyposis,
+BMGC_DS18992,BMG_DS072646,,,,,,,,,C5679618,,,MONDO:0016600,acute neonatal citrullinemia type I,
+BMGC_DS18993,BMG_DS072651,,,,,,,,,C5679639,,,MONDO:0016780,paternal 14q32.2 microdeletion syndrome,
+BMGC_DS18994,BMG_DS072652,,,,,,,,,C5679640,,,MONDO:0016781,maternal 14q32.2 microdeletion syndrome,
+BMGC_DS18995,BMG_DS072683,,,,,,,,,C5679679,,,MONDO:0016861,Alagille syndrome due to 20p12 microdeletion,
+BMGC_DS18996,BMG_DS072684,,,,,,,,,C5679681,,,MONDO:0016856,Mowat-Wilson syndrome due to a ZEB2 point mutation,
+BMGC_DS18997,BMG_DS072685,,,,,,,,,C5679682,,,MONDO:0016863,Okihiro syndrome due to 20q13 microdeletion,
+BMGC_DS18998,BMG_DS072686,,,,,,,,,C5679683,,,MONDO:0016864,Okihiro syndrome due to a point mutation,
+BMGC_DS18999,BMG_DS072692,,,,,,,DOID:0070520,peeling skin syndrome 1,C5679693,,,,,
+BMGC_DS19000,BMG_DS072722,,,,,,,,,C5679767,,,MONDO:0017096,isolated focal cortical dysplasia type Ia,
+BMGC_DS19001,BMG_DS072723,,,,,,,,,C5679768,,,MONDO:0017102,isolated focal cortical dysplasia type IIb,
+BMGC_DS19002,BMG_DS072725,,,,,,,,,C5679774,,,MONDO:0017116,congenital communicating hydrocephalus,
+BMGC_DS19003,BMG_DS072726,,,,,,,,,C5679776,,,MONDO:0017221,"Pelizaeus-Merzbacher disease, connatal form",
+BMGC_DS19004,BMG_DS072729,,,,,,,,,C5679780,,,MONDO:0017172,"mucopolysaccharidosis type 6, slowly progressing",
+BMGC_DS19005,BMG_DS072730,,,,,,,,,C5679781,,,MONDO:0017171,"mucopolysaccharidosis type 6, rapidly progressing",
+BMGC_DS19006,BMG_DS072731,,,,,,,,,C5679782,,,MONDO:0016073,syndromic microphthalmia,
+BMGC_DS19007,BMG_DS072735,,,,,,,,,C5679787,,,MONDO:0016147,qualitative or quantitative defects of dystrophin,
+BMGC_DS19008,BMG_DS072736,,,,,,,,,C5679788,,,MONDO:0100228,LAMA2-related muscular dystrophy,
+BMGC_DS19009,BMG_DS072737,,,,,,,,,C5679790,,,MONDO:0016146,caveolinopathy,
+BMGC_DS19010,BMG_DS072740,,,,,,,,,C5679802,,,MONDO:0016248,familial ovarian cancer,
+BMGC_DS19011,BMG_DS072741,,,,,,,,,C5679804,,,MONDO:0016268,papillary carcinoma of the corpus uteri,
+BMGC_DS19012,BMG_DS072744,,,,,,,,,C5679810,,,MONDO:0016302,isolated congenitally uncorrected transposition of the great arteries,
+BMGC_DS19013,BMG_DS072746,,,,,,,,,C5679812,,,MONDO:0016304,classic pantothenate kinase-associated neurodegeneration,
+BMGC_DS19014,BMG_DS072747,,,,,,,,,C5679813,,,MONDO:0016309,"Niemann-Pick disease type C, juvenile neurologic onset",
+BMGC_DS19015,BMG_DS072748,,,,,,,,,C5679814,,,MONDO:0016311,Bockenheimer syndrome,
+BMGC_DS19016,BMG_DS072749,,,,,,,,,C5679815,,,MONDO:0016316,"mucopolysaccharidosis type 2, attenuated form",
+BMGC_DS19017,BMG_DS072750,1197205005,Combined immunodeficiency due to DOCK8 deficiency,,,,,,,C5679816,,,,,Combined immunodeficiency due to DOCK8 deficiency | Combined immunodeficiency due to dedicator of cytokinesis 8 deficiency | Combined immunodeficiency due to dedicator of cytokinesis 8 deficiency (disorder) | Combined immunodeficiency due to dedicator of cytokinesis 8 protein deficiency | DOCK8 immunodeficiency syndrome
+BMGC_DS19018,BMG_DS072752,,,,,,,,,C5679825,,,MONDO:0016387,mitochondrial oxidative phosphorylation disorder,
+BMGC_DS19019,BMG_DS072754,,,,,,,,,C5679828,,,MONDO:0016764,isolated anophthalmia-microphthalmia syndrome,
+BMGC_DS19020,BMG_DS072755,,,,,,,,,C5679833,,,MONDO:0016502,Hermansky-Pudlak syndrome without pulmonary fibrosis,
+BMGC_DS19021,BMG_DS072756,,,,,,,,,C5679834,,,MONDO:0016501,Hermansky-Pudlak syndrome with pulmonary fibrosis,
+BMGC_DS19022,BMG_DS072761,,,,,,,,,C5679845,,,MONDO:0016533,apolipoprotein A-II amyloidosis,
+BMGC_DS19023,BMG_DS072762,1231284001,Autosomal dominant generalized dystrophic epidermolysis bullosa,,,,,,,C5679846,,,,,Autosomal dominant generalized dystrophic epidermolysis bullosa (disorder) | Generalised DDEB (generalised dystrophic epidermolysis bullosa) | Generalized DDEB (generalized dystrophic epidermolysis bullosa) | Autosomal dominant generalized dystrophic epidermolysis bullosa | Autosomal dominant generalised dystrophic epidermolysis bullosa | DDEB (dominant dystrophic epidermolysis bullosa) intermediate
+BMGC_DS19024,BMG_DS072764,,,,,,,,,C5679849,,,MONDO:0016553,isolated congenital hypogonadotropic hypogonadism,
+BMGC_DS19025,BMG_DS072765,,,,,,,,,C5679850,,,MONDO:0016564,progressive supranuclear palsy-progressive non-fluent aphasia syndrome,
+BMGC_DS19026,BMG_DS072766,,,,,,,,,C5679851,,,MONDO:0016562,progressive supranuclear palsy-pure akinesia with gait freezing syndrome,
+BMGC_DS19027,BMG_DS072768,,,,,,,,,C5679855,,,MONDO:0018022,hemoglobin Lepore-beta-thalassemia syndrome,
+BMGC_DS19028,BMG_DS072771,,,,,,,,,C5679860,,,MONDO:0018004,acute megakaryoblastic leukemia without down syndrome,
+BMGC_DS19029,BMG_DS072772,,,,,,,,,C5679869,,,MONDO:0017972,classic congenital lipoid adrenal hyperplasia due to STAR deficency,
+BMGC_DS19030,BMG_DS072774,,,,,,,,,C5679882,,,MONDO:0017945,ABetaL34V amyloidosis,
+BMGC_DS19031,BMG_DS072775,,,,,,,,,C5679883,,,MONDO:0017939,classic multiminicore myopathy,
+BMGC_DS19032,BMG_DS072776,1197217007,Multiple paraganglioma associated with polycythemia,,,,,,,C5679884,,,MONDO:0017926,multiple paragangliomas associated with polycythemia,"Paraganglioma, somatostatinoma, polycythemia syndrome | Multiple paraganglioma associated with polycythaemia | Multiple paraganglioma associated with erythrocytosis | Paraganglioma, somatostatinoma, polycythaemia syndrome | Multiple paraganglioma associated with polycythemia (disorder) | Multiple paraganglioma associated with polycythemia"
+BMGC_DS19033,BMG_DS072781,,,,,,,,,C5679895,,,MONDO:0017840,"classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form",
+BMGC_DS19034,BMG_DS072782,,,,,,,,,C5679896,,,MONDO:0017839,"classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form",
+BMGC_DS19035,BMG_DS072784,1264010001,Primary hypereosinophilic syndrome,,,,,,,C5679898,,,MONDO:0017833,primary hypereosinophilic syndrome,Primary hypereosinophilic syndrome | Primary hypereosinophilic syndrome (disorder) | Clonal hypereosinophilic syndrome | Neoplastic hypereosinophilic syndrome | Primary HES (hypereosinophilic syndrome) | HES-N - hypereosinophilic syndrome neoplastic
+BMGC_DS19036,BMG_DS072786,,,,,,,,,C5679900,,,MONDO:0017847,autosomal recessive spastic ataxia,
+BMGC_DS19037,BMG_DS072788,,,,,,,,,C5679911,,,MONDO:0018276,muscular dystrophy-dystroglycanopathy,
+BMGC_DS19038,BMG_DS072789,1208937004,"Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies",,,,,,,C5679913,,,,,"Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies | mtDNA (mitochondrial deoxyribonucleic acid) depletion syndrome, encephalomyopathic form with variable craniofacial anomalies | Mitochondrial deoxyribonucleic acid depletion syndrome, encephalomyopathic form with variable craniofacial anomalies | Mitochondrial deoxyribonucleic acid depletion syndrome, encephalomyopathic form with variable craniofacial anomalies (disorder)"
+BMGC_DS19039,BMG_DS072790,1332388003,Alexander disease type II,,,,,,,C5679914,,,MONDO:0018210,Alexander disease type II,Alexander disease type II | AxD (Alexander disease) type II | Alexander disease type II (disorder)
+BMGC_DS19040,BMG_DS072791,1269225005,Hemolytic uremic syndrome with DGKE deficiency,,,,,,,C5679921,,,MONDO:0018159,atypical hemolytic-uremic syndrome with DGKE deficiency,Hemolytic uremic syndrome with diacylglycerol kinase epsilon deficiency | Hemolytic uremic syndrome with diacylglycerol kinase epsilon deficiency (disorder) | Haemolytic uraemic syndrome with DGKE deficiency | Hemolytic uremic syndrome with DGKE deficiency | Haemolytic uraemic syndrome with diacylglycerol kinase epsilon deficiency
+BMGC_DS19041,BMG_DS072792,,,,,,,,,C5679922,,,MONDO:0009054,"autosomal recessive cutis laxa type 2, classic type",
+BMGC_DS19042,BMG_DS072793,,,,,,,,,C5679923,,,MONDO:0018136,minimal pigment oculocutaneous albinism type 1,
+BMGC_DS19043,BMG_DS072794,,,,,,,,,C5679925,,,MONDO:0018131,neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion,
+BMGC_DS19044,BMG_DS072795,,,,,,,,,C5679927,,,MONDO:0018143,"pyruvate carboxylase deficiency, benign type",
+BMGC_DS19045,BMG_DS072796,,,,,,,,,C5679928,,,MONDO:0018141,"pyruvate carboxylase deficiency, infantile form",
+BMGC_DS19046,BMG_DS072797,,,,,,,,,C5679929,,,MONDO:0018142,"pyruvate carboxylase deficiency, severe neonatal type",
+BMGC_DS19047,BMG_DS072806,,,,,,,,,C5679943,,,MONDO:0017383,familial clubfoot due to PITX1 point mutation,
+BMGC_DS19048,BMG_DS072807,,,,,,,,,C5679944,,,MONDO:0017382,familial clubfoot due to 5q31 microdeletion,
+BMGC_DS19049,BMG_DS072808,,,,,,,,,C5679945,,,MONDO:0017389,tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria,
+BMGC_DS19050,BMG_DS072810,1208933000,4H leukodystrophy,,,,,,,C5679947,,,MONDO:0700282,POLR3-related leukodystrophy,4H leukodystrophy (disorder) | 4H leucodystrophy | 4H leukodystrophy | POLR-related leucodystrophy | POLR-related leukodystrophy
+BMGC_DS19051,BMG_DS072812,,,,,,,,,C5679949,,,MONDO:0017244,pseudoxanthomatous diffuse cutaneous mastocytosis,
+BMGC_DS19052,BMG_DS072818,,,,,,,,,C5679956,,,MONDO:0017683,methylcobalamin deficiency type cblDv1,
+BMGC_DS19053,BMG_DS072819,,,,,,,,,C5679969,,,MONDO:0017699,"glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form",
+BMGC_DS19054,BMG_DS072820,,,,,,,,,C5679972,,,MONDO:0017695,"glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form",
+BMGC_DS19055,BMG_DS072821,,,,,,,,,C5679974,,,MONDO:0017733,"alpha-mannosidosis, adult form",
+BMGC_DS19056,BMG_DS072825,,,,,,,,,C5679983,,,MONDO:0017544,zygodactyly type 3,
+BMGC_DS19057,BMG_DS072828,1237181009,Symptomatic form of hemochromatosis type 1,,,,,,,C5679990,,,,,Symptomatic form of hemochromatosis type 1 (disorder) | Symptomatic form of classic hemochromatosis | Symptomatic form of hemochromatosis type 1 | Symptomatic form of classic haemochromatosis | Symptomatic form of haemochromatosis type 1
+BMGC_DS19058,BMG_DS072829,,,,,,,,,C5679991,,,MONDO:0018733,intellectual disability syndrome due to a DYRK1A point mutation,
+BMGC_DS19059,BMG_DS072831,,,,,,,,,C5679993,,,MONDO:0018698,hereditary neuroendocrine tumor of small intestine,
+BMGC_DS19060,BMG_DS072832,1237623009,Congenital insensitivity to pain with severe intellectual disability,,,,,,,C5679994,,,MONDO:0018682,congenital insensitivity to pain with severe intellectual disability,Congenital analgesia with severe intellectual disability | Congenital absence of pain with severe intellectual disability | Congenital insensitivity to pain with severe intellectual disability (disorder) | Congenital insensitivity to pain with severe intellectual disability | Congenital insensitivity to pain with preserved temperature sensation | Congenital insensitivity to pain with severe non-progressive cognitive delay
+BMGC_DS19061,BMG_DS072834,1229883008,19p13.3 microduplication syndrome,,,,,,,C5679996,,,MONDO:0018658,19p13.3 microduplication syndrome,19p13.3 microduplication syndrome (disorder) | 19p13.3 microduplication syndrome
+BMGC_DS19062,BMG_DS072841,,,,,,,,,C5680012,,,MONDO:0018426,AXIN2-related attenuated familial adenomatous polyposis,
+BMGC_DS19063,BMG_DS072843,,,,,,,,,C5680016,,,MONDO:0018463,mild phosphoribosylpyrophosphate synthetase superactivity,
+BMGC_DS19064,BMG_DS072844,,,,,,,,,C5680017,,,MONDO:0018464,severe phosphoribosylpyrophosphate synthetase superactivity,
+BMGC_DS19065,BMG_DS072847,,,,,,,,,C5680024,,,MONDO:0018324,adult-onset myasthenia gravis,
+BMGC_DS19066,BMG_DS072848,,,,,,,,,C5680025,,,MONDO:0018322,"HSD10 disease, infantile type",
+BMGC_DS19067,BMG_DS072849,,,,,,,,,C5680026,,,MONDO:0018323,"HSD10 disease, neonatal type",
+BMGC_DS19068,BMG_DS072850,,,,,,,,,C5680028,,,MONDO:0018333,"multiple acyl-CoA dehydrogenase deficiency, mild type",
+BMGC_DS19069,BMG_DS072851,,,,,,,,,C5680029,,,MONDO:0018332,"multiple acyl-CoA dehydrogenase deficiency, severe neonatal type",
+BMGC_DS19070,BMG_DS072857,1229943004,SIM1-related Prader-Willi-like syndrome,,,,,,,C5680040,,,MONDO:0018355,SIM1-related Prader-Willi-like syndrome,SIM bHLH transcription factor 1-related Prader-Willi-like syndrome | SIM1-related Prader-Willi-like syndrome | SIM bHLH transcription factor 1-related Prader-Willi-like syndrome (disorder)
+BMGC_DS19071,BMG_DS072860,1197593006,"Intellectual disability, expressive aphasia, facial dysmorphism syndrome",,,,,,,C5680043,,,,,"Intellectual disability, expressive aphasia, facial dysmorphism syndrome (disorder) | Intellectual disability, loss of expressive language, facial dysmorphism syndrome | Intellectual disability, expressive aphasia, facial dysmorphism syndrome"
+BMGC_DS19072,BMG_DS072861,1197428008,"Combined immunodeficiency, enteropathy spectrum",,,,,,,C5680044,,243150,MONDO:0800030,gastrointestinal defects and immunodeficiency syndrome 1,"CID-MIA/early-onset IBD - combined immunodeficiency-multiple intestinal atresia/early-onset inflammatory bowel disease | Combined immunodeficiency, enteropathy spectrum | Combined immunodeficiency, enteropathy spectrum (disorder)"
+BMGC_DS19073,BMG_DS072862,1220599002,Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa,,,,,,,C5680045,,,MONDO:0018577,pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa,PXE-like (pseudoxanthoma elasticum-like) syndrome with retinitis pigmentosa | Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa (disorder) | Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa
+BMGC_DS19074,BMG_DS072863,1197366007,Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity,,,,,,,C5680046,,,,,Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity | Autosomal recessive primary immunodeficiency with defective spontaneous NK (natural killer) cell cytotoxicity | CD16 deficiency | Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity (disorder)
+BMGC_DS19075,BMG_DS072872,1229999001,"Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome",,,,,,,C5680056,,,MONDO:0018601,autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome,"Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome (disorder) | Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome | Autosomal dominant myopia, midfacial retrusion, sensorineural deafness, rhizomelic dysplasia syndrome"
+BMGC_DS19076,BMG_DS072873,,,,,,,,,C5680057,,,MONDO:0018614,undetermined early-onset epileptic encephalopathy,
+BMGC_DS19077,BMG_DS072876,1217211002,Postural orthostatic tachycardia syndrome due to norepinephrine transporter deficiency,,,,,,,C5680060,,,,,Postural orthostatic tachycardia syndrome due to NET (norepinephrine transporter) deficiency | Postural orthostatic tachycardia syndrome due to norepinephrine transporter deficiency | Familial orthostatic tachycardia due to norepinephrine transporter deficiency | Orthostatic intolerance due to NET (norepinephrine transporter) deficiency | Postural orthostatic tachycardia syndrome due to norepinephrine transporter deficiency (disorder) | POTS (postural orthostatic tachycardia syndrome) due to NET (norepinephrine transporter) deficiency
+BMGC_DS19078,BMG_DS072881,1197478005,Primary immunodeficiency with multifaceted aberrant lymphoid immunity,,,,,,,C5680065,,,MONDO:0018642,NIK deficiency,Primary immunodeficiency with multifaceted aberrant lymphoid immunity | NIK deficiency | NF-kappa-B-inducing kinase deficiency | Primary immunodeficiency with multifaceted aberrant lymphoid immunity (disorder)
+BMGC_DS19079,BMG_DS072882,,,,,,,,,C5680067,,,MONDO:0018656,tremor-ataxia-central hypomyelination syndrome,
+BMGC_DS19080,BMG_DS072888,1222671009,3-methylglutaconic aciduria type 8,,,,,,,C5680084,,,,,3-methylglutaconic aciduria type 8 | 3-methylglutaconic aciduria type 8 (disorder)
+BMGC_DS19081,BMG_DS072889,1228886008,9q33.3q34.11 microdeletion syndrome,,,,,,,C5680085,,,MONDO:0044641,9q33.3q34.11 microdeletion syndrome,9q33.3q34.11 microdeletion syndrome | Deletion 9q33.3q34.11 | 9q33.3q34.11 microdeletion syndrome (disorder) | Monosomy 9q33.3q34.11
+BMGC_DS19082,BMG_DS072890,1228890005,16p13.2 microdeletion syndrome,,,,,,,C5680086,,,MONDO:0100528,Hao-Fountain syndrome due to 16p13.2 microdeletion,16p13.2 microdeletion syndrome (disorder) | 16p13.2 microdeletion syndrome | Monosomy 16p13.2
+BMGC_DS19083,BMG_DS072893,1251451005,MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome,,,,,,,C5680092,,,MONDO:0044682,MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome,Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome (disorder) | Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome | MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome
+BMGC_DS19084,BMG_DS072896,,,,,,,,,C5680095,,,MONDO:0018841,congenital bile acid synthesis defect,
+BMGC_DS19085,BMG_DS072899,,,,,,,,,C5680100,,,MONDO:0018804,MYO5B-related progressive familial intrahepatic cholestasis,
+BMGC_DS19086,BMG_DS072901,,,,,,,,,C5680106,,,MONDO:0018776,demyelinating hereditary motor and sensory neuropathy,
+BMGC_DS19087,BMG_DS072905,1222709003,Syndromic congenital sodium diarrhea,,,,,,,C5680120,,,MONDO:0034204,syndromic congenital sodium diarrhea,Syndromic congenital sodium diarrhoea | Syndromic congenital sodium diarrhea | Syndromic congenital sodium diarrhea (disorder) | Syndromic congenital tufting enteropathy
+BMGC_DS19088,BMG_DS072909,1279844009,Primary triglyceride deposit cardiomyovasculopathy,,,,,,,C5680124,,,MONDO:0035423,triglyceride deposit cardiomyovasculopathy,Primary triglyceride deposit cardiomyovasculopathy (disorder) | Primary triglyceride deposit cardiomyovasculopathy | Neutral lipid storage disease with severe cardiovascular involvement
+BMGC_DS19089,BMG_DS072912,1260240000,Resistance to thyroid hormone due to mutation in thyroid hormone receptor alpha,,,,,,,C5680127,,,MONDO:0034216,resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha,Resistance to thyroid hormone due to mutation in thyroid hormone receptor alpha | Resistance to thyroid hormone due to mutation in thyroid hormone receptor alpha (disorder) | Resistance to thyroid hormone alpha | Resistance to thyroid hormone due to mutation in TRa
+BMGC_DS19090,BMG_DS072913,,,,,,,,,C5680128,,,MONDO:0035444,acute mast cell leukemia,
+BMGC_DS19091,BMG_DS072914,1208617001,Congenital autosomal recessive small-platelet thrombocytopenia,,,,,,,C5680129,,,MONDO:0035441,congenital autosomal recessive small-platelet thrombocytopenia,Congenital autosomal recessive small-platelet thrombocytopenia (disorder) | Congenital autosomal recessive small-platelet thrombocytopenia | CARST - congenital autosomal recessive small-platelet thrombocytopenia
+BMGC_DS19092,BMG_DS072915,,,,,,,,,C5680130,,,MONDO:0035445,chronic mast cell leukemia,
+BMGC_DS19093,BMG_DS072919,1197746001,AKT2-related familial partial lipodystrophy,,,,,,,C5680134,,,MONDO:0019192,AKT2-related familial partial lipodystrophy,AKT serine/threonine kinase 2-related familial partial lipodystrophy | AKT2-related familial partial lipodystrophy | AKT serine/threonine kinase 2-related familial partial lipodystrophy (disorder)
+BMGC_DS19094,BMG_DS072921,1222669009,Congenital primary lymphedema of Gordon,,,,,,,C5680138,,,MONDO:0035500,congenital primary lymphedema of Gordon,VEGFC-related congenital primary lymphedema | Congenital primary lymphedema of Gordon (disorder) | Congenital primary lymphedema of Gordon | Congenital primary lymphoedema of Gordon | VEGFC-related congenital primary lymphoedema
+BMGC_DS19095,BMG_DS072922,1222666002,EPHB4-related lymphatic-related hydrops fetalis,,,,,,,C5680140,,,MONDO:0035475,EPHB4-related lymphatic-related hydrops fetalis,Ephrin receptor B4-related lymphatic-related hydrops fetalis | Ephrin receptor B4-related lymphatic-related hydrops fetalis (disorder) | EPHB4-related lymphatic-related hydrops fetalis | EPHB4-related generalised lymphatic dysplasia with non-immune hydrops fetalis | EPHB4-related generalized lymphatic dysplasia with non-immune hydrops fetalis | EPHB4-related generalised lymphatic dysplasia with atrial septal defect | EPHB4-related generalized lymphatic dysplasia with atrial septal defect
+BMGC_DS19096,BMG_DS072923,1222645005,KRT1-related diffuse nonepidermolytic keratoderma,,,,,DOID:0070550,KRT1-related nonepidermolytic palmoplantar keratoderma,C5680142,,,,,KRT1-related diffuse nonepidermolytic keratoderma | Keratin 1-related diffuse nonepidermolytic palmoplantar keratoderma (disorder) | Keratin 1-related diffuse nonepidermolytic palmoplantar keratoderma | KRT1-related diffuse NEPPK (nonepidermolytic palmoplantar keratoderma)
+BMGC_DS19097,BMG_DS072924,,,,,,,,,C5680143,,,MONDO:0035161,progressive dementia with neuroserpin inclusion bodies,
+BMGC_DS19098,BMG_DS072925,,,,,,,,,C5680148,,,MONDO:0018162,neurometabolic disorder due to serine deficiency,
+BMGC_DS19099,BMG_DS072927,1255116001,Myopathic Ehlers-Danlos syndrome,,,,,,,C5680153,,,,,Myopathic EDS (Ehlers-Danlos syndrome) | Myopathic Ehlers-Danlos syndrome (disorder) | Myopathic Ehlers-Danlos syndrome | Ehlers-Danlos myopathy overlap syndrome
+BMGC_DS19100,BMG_DS072929,,,,,,,,,C5680155,,,MONDO:0035220,PLG-related hereditary angioedema with normal C1inh,
+BMGC_DS19101,BMG_DS072930,1256055008,Ulcerative pyoderma gangrenosum,,,,,,,C5680157,,,MONDO:0035235,classic pyoderma gangrenosum,Ulcerative pyoderma gangrenosum | Ulcerative pyoderma gangrenosum (disorder)
+BMGC_DS19102,BMG_DS072931,,,,,,,,,C5680158,,,MONDO:0035238,vegetative pyoderma gangrenosum,
+BMGC_DS19103,BMG_DS072933,1222656005,SYNGAP1-related developmental and epileptic encephalopathy,,,,,,,C5680163,,,MONDO:0034099,SYNGAP1-related developmental and epileptic encephalopathy,Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy (disorder) | SYNGAP1-related developmental and epileptic encephalopathy | Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy
+BMGC_DS19104,BMG_DS072936,1293264009,Atypical hemolytic uremic syndrome with complement gene abnormality,,,,,,,C5680166,,,MONDO:0035290,atypical hemolytic uremic syndrome with complement gene abnormality,Atypical haemolytic uraemic syndrome with complement gene abnormality | Atypical hemolytic uremic syndrome with complement gene abnormality (disorder) | Atypical hemolytic uremic syndrome with complement gene abnormality | aHUS (atypical haemolytic uraemic syndrome) with complement gene abnormality | aHUS (atypical hemolytic uremic syndrome) with complement gene abnormality
+BMGC_DS19105,BMG_DS072938,,,,,,,,,C5680171,,,MONDO:0035320,early-onset familial hypoaldosteronism,
+BMGC_DS19106,BMG_DS072940,,,,,,,,,C5680178,,,MONDO:0019548,autosomal dominant intermediate Charcot-Marie-Tooth disease,
+BMGC_DS19107,BMG_DS072942,1279831004,"Congenital insensitivity to pain, anosmia, neuropathic arthropathy",,,,,,,C5680180,,,,,"Sodium voltage-gated channel alpha subunit 9-related congenital insensitivity to pain | Congenital insensitivity to pain, anosmia, neuropathic arthropathy | SCN9A-related congenital insensitivity to pain | Congenital insensitivity to pain, anosmia, neuropathic arthropathy (disorder)"
+BMGC_DS19108,BMG_DS072943,,,,,,,,,C5680181,,,MONDO:0019502,autosomal recessive non-syndromic intellectual disability,
+BMGC_DS19109,BMG_DS072944,1260199008,Non-syndromic genetic hearing loss,,,,,,,C5680182,,,MONDO:0019497,nonsyndromic genetic hearing loss,Non-syndromic genetic deafness | Non-syndromic genetic hearing loss | Non-syndromic genetic hearing loss (disorder) | Isolated genetic hearing loss | Isolated genetic deafness
+BMGC_DS19110,BMG_DS072945,1260142000,"Congenital vertebral, cardiac, renal anomalies syndrome",,,,,,,C5680183,,,MONDO:0020831,congenital vertebral-cardiac-renal anomalies syndrome,"Congenital vertebral, cardiac, renal anomalies syndrome (disorder) | Congenital NAD deficiency disorder | Congenital vertebral, cardiac, renal anomalies syndrome"
+BMGC_DS19111,BMG_DS072946,1229873009,17q24.2 microdeletion syndrome,,,,,,,C5680185,,,MONDO:0035151,17q24.2 microdeletion syndrome,17q24.2 microdeletion syndrome (disorder) | 17q24.2 microdeletion syndrome
+BMGC_DS19112,BMG_DS072948,,,,,,,,,C5680192,,,MONDO:0019586,X-linked nonsyndromic hearing loss,
+BMGC_DS19113,BMG_DS072949,1230014007,Duane retraction syndrome with congenital deafness,,,,,,,C5680193,,,MONDO:0035337,Duane retraction syndrome with congenital deafness,Duane retraction syndrome with congenital deafness | Duane retraction syndrome with congenital deafness (disorder) | Duane retraction syndrome with congenital hearing loss
+BMGC_DS19114,BMG_DS072952,,,,,,,,,C5680203,,,MONDO:0019258,mild phenylketonuria,
+BMGC_DS19115,BMG_DS072954,,,,,,,,,C5680206,,,MONDO:0037149,"HSD10 disease, atypical type",
+BMGC_DS19116,BMG_DS072955,,,,,,,,,C5680207,,,MONDO:0019335,mild hyperphenylalaninemia,
+BMGC_DS19117,BMG_DS072957,1300133004,KLHL7-related Bohring Opitz-like syndrome,,,,,,,C5680210,,,MONDO:0035823,KLHL7-related Bohring-Opitz-like syndrome,KLHL7-related Bohring Opitz-like syndrome | Kelch like family member 7-related Bohring Opitz-like syndrome | Kelch like family member 7-related Bohring Opitz-like syndrome (disorder) | KLHL7 (kelch like family member 7) related Bohring Opitz-like syndrome
+BMGC_DS19118,BMG_DS072958,1304117006,KLHL7-related Crisponi/cold-induced sweating-like syndrome,,,,,,,C5680211,,,MONDO:0035824,KLHL7-related cold-induced sweating-like syndrome,KLHL7-related Crisponi-like syndrome | Kelch like family member 7-related Crisponi/cold-induced sweating-like syndrome (disorder) | Kelch like family member 7-related Crisponi/cold-induced sweating-like syndrome | KLHL7-related Crisponi/cold-induced sweating-like syndrome | KLHL7 (kelch like family member 7) related Crisponi/cold-induced sweating-like syndrome
+BMGC_DS19119,BMG_DS072965,,,,,,,,,C5680247,,,MONDO:0019913,silver-Russell syndrome due to maternal uniparental disomy of chromosome 7,
+BMGC_DS19120,BMG_DS072966,,,,,,,,,C5680248,,,MONDO:0019915,maternal uniparental disomy of chromosome 14,
+BMGC_DS19121,BMG_DS072968,,,,,,,,,C5680251,,608149,MONDO:0011975,paternal uniparental disomy of chromosome 14,
+BMGC_DS19122,BMG_DS072977,,,,,,,,,C5680265,,,MONDO:0036045,euthyroid dysprealbuminemic hyperthyroxinemia,
+BMGC_DS19123,BMG_DS072978,,,,,,,,,C5680266,,,MONDO:0036042,KAT6B-related multiple congenital anomalies syndrome,
+BMGC_DS19124,BMG_DS072979,,,,,,,,,C5680267,,,MONDO:0019733,AFib amyloidosis,
+BMGC_DS19125,BMG_DS072981,,,,,,,,,C5680269,,,MONDO:0019731,AApoAI amyloidosis,
+BMGC_DS19126,BMG_DS072982,,,,,,,,,C5680270,,,MONDO:0019732,ALys amyloidosis,
+BMGC_DS19127,BMG_DS072985,1300130001,Hypomyelination of early myelinating structures,,,,,,,C5680278,,,,,Hypomyelination of early myelinating structures (disorder) | Hypomyelination of early myelinating structures | HEMS - hypomyelination of early myelinating structures
+BMGC_DS19128,BMG_DS072991,1336027001,Combined immunodeficiency due to RELA haploinsufficiency,,,,,,,C5680288,,,MONDO:0035694,combined immunodeficiency due to RELA haploinsufficiency,Combined immunodeficiency due to RELA haploinsufficiency (disorder) | Combined immunodeficiency due to RELA haploinsufficiency
+BMGC_DS19129,BMG_DS072993,,,,,,,,,C5680290,,,MONDO:0020407,complete atrioventricular canal-ventricle hypoplasia syndrome,
+BMGC_DS19130,BMG_DS072997,,,,,,,,,C5680294,,,MONDO:0020437,"atrial septal defect, ostium primum type",
+BMGC_DS19131,BMG_DS073004,1281842000,"GNAO1-related developmental delay, seizures, movement disorder spectrum",,,,,,,C5680303,,,MONDO:0035660,GNAO1-related developmental delay-seizures-movement disorder spectrum,"G protein subunit alpha o1-related developmental delay, seizures, movement disorder spectrum (disorder) | GNAO1-related developmental delay, seizures, movement disorder spectrum | GNAO1-related spectrum | G protein subunit alpha o1-related developmental delay, seizures, movement disorder spectrum"
+BMGC_DS19132,BMG_DS073005,,,,,,,,,C5680305,,,MONDO:0035646,congenital-onset Steinert myotonic dystrophy,
+BMGC_DS19133,BMG_DS073006,,,,,,,,,C5680306,,,MONDO:0035648,juvenile-onset Steinert myotonic dystrophy,
+BMGC_DS19134,BMG_DS073007,,,,,,,,,C5680307,,,MONDO:0035647,childhood-onset Steinert myotonic dystrophy,
+BMGC_DS19135,BMG_DS073008,,,,,,,,,C5680308,,,MONDO:0035650,late-onset Steinert myotonic dystrophy,
+BMGC_DS19136,BMG_DS073009,,,,,,,,,C5680309,,,MONDO:0035649,adult-onset Steinert myotonic dystrophy,
+BMGC_DS19137,BMG_DS073010,1281843005,"Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome",,,,,,,C5680310,,620186,MONDO:0035651,choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome,"Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome (disorder) | Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome | Lysine methyltransferase 2D-related choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome | KMT2D-related choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome"
+BMGC_DS19138,BMG_DS073011,1208985003,"Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies",,,,,,,C5680313,,,MONDO:0035124,"linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies","Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies | Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies (disorder) | RHOA (ras homolog family member A) related mosaic ectodermal dysplasia | RHOA-related mosaic ectodermal dysplasia"
+BMGC_DS19139,BMG_DS073012,,,,,,,DOID:0080643,B-lymphoblastic leukemia/lymphoma with BCR-ABL1,C5680319,,,MONDO:0035940,B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2),
+BMGC_DS19140,BMG_DS073013,,,,,,,DOID:0080649,B-lymphoblastic leukemia/lymphoma with TCF3-PBX1,C5680320,,,,,
+BMGC_DS19141,BMG_DS073015,1197151003,Autosomal recessive isolated optic atrophy,,,,,,,C5680331,,,,,Autosomal recessive isolated optic atrophy (disorder) | Autosomal recessive isolated optic atrophy | Autosomal recessive non-syndromic optic atrophy
+BMGC_DS19142,BMG_DS073016,,,,,,,,,C5680338,,,MONDO:0035930,neu-laxova syndrome due to 3-phosphoserine phosphatase deficiency,
+BMGC_DS19143,BMG_DS073019,,,,,,,,,C5680342,,,MONDO:0020303,Angelman syndrome due to paternal uniparental disomy of chromosome 15,
+BMGC_DS19144,BMG_DS073020,,,,,,,,,C5680343,,,MONDO:0020298,Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15,
+BMGC_DS19145,BMG_DS073021,1197429000,"Cathepsin A-related arteriopathy, strokes, leukoencephalopathy",,,,,,,C5680354,,,MONDO:0035551,cathepsin a-related arteriopathy-strokes-leukoencephalopathy,"Cathepsin A-related arteriopathy, strokes, leucoencephalopathy | Cathepsin A-related arteriopathy, strokes, leukoencephalopathy | CARASAL - cathepsin A-related arteriopathy, strokes, leukoencephalopathy | Cathepsin A-related arteriopathy, strokes, leukoencephalopathy (disorder) | CARASAL - cathepsin A-related arteriopathy, strokes, leucoencephalopathy"
+BMGC_DS19146,BMG_DS073024,1279842008,Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial JAK1 deficiency,,,,,,,C5680361,,,MONDO:0035548,autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiency,Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial JAK1 deficiency | Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial janus kinase 1 deficiency (disorder) | Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial janus kinase 1 deficiency
+BMGC_DS19147,BMG_DS073025,,,,,,,,,C5680363,,,MONDO:0035525,blepharophimosis-ptosis-epicanthus inversus syndrome type 2,
+BMGC_DS19148,BMG_DS073026,1197476009,"Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia",,,,,,,C5680364,,,MONDO:0035529,infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia,"2'-5'-oligoadenylate synthetase 1-related infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | OAS1-related infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia | Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia (disorder) | OAS1-related infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | 2'-5'-oligoadenylate synthetase 1-related infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia | Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia"
+BMGC_DS19149,BMG_DS073027,,,,,,,,,C5680365,,,MONDO:0035524,blepharophimosis-ptosis-epicanthus inversus syndrome type 1,
+BMGC_DS19150,BMG_DS073036,,,,,,,,,C5680385,,,MONDO:0036218,lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene cluster,
+BMGC_DS19151,BMG_DS073047,,,,,,,,,C5680398,,,MONDO:0850078,non-syndromic non-specific multisutural craniosynostosis,
+BMGC_DS19152,BMG_DS073061,,,,,,,,,C5680412,,,MONDO:0850096,SBDS-related severe neonatal spondylometaphyseal dysplasia,
+BMGC_DS19153,BMG_DS073062,,,,,,,,,C5680413,,,MONDO:0850067,immune deficiency due to impaired neutrophil phagocytosis and migration,
+BMGC_DS19154,BMG_DS073063,,,,,,,,,C5680414,,,MONDO:0850066,SAMD9L-associated autoinflammatory syndrome,
+BMGC_DS19155,BMG_DS073064,,,,,,,,,C5680415,,,MONDO:0850069,familial hyperinflammatory lymphoproliferative immunodeficiency,
+BMGC_DS19156,BMG_DS073065,,,,,,,,,C5680416,,,MONDO:0850068,early-onset autoimmunity-autoinflammation-immunodeficiency syndrome,
+BMGC_DS19157,BMG_DS073066,1336113009,CADINS disease,,,,,,,C5680417,,,MONDO:0850070,CADINS disease,Caspase recruitment domain family member 11-associated atopy with dominant interference of nuclear factor kappa-B signaling syndrome (disorder) | Caspase recruitment domain family member 11-associated atopy with dominant interference of nuclear factor kappa-B signaling syndrome | CARD11-associated atopy with dominant interference of NF-kB signaling syndrome | CADINS disease
+BMGC_DS19158,BMG_DS073068,1303868000,Intermediate DEND syndrome,,,,,,,C5680423,,,MONDO:0020569,intermediate DEND syndrome,"Intermediate DEND syndrome | Developmental delay, epilepsy, neonatal diabetes syndrome, intermediate form (disorder) | Developmental delay, epilepsy, neonatal diabetes syndrome, intermediate form | Intermediate DEND (developmental delay, epilepsy, neonatal diabetes) syndrome"
+BMGC_DS19159,BMG_DS073072,1197157004,Severe congenital nemaline myopathy,,,,,,,C5680451,,,MONDO:0015735,severe congenital nemaline myopathy,Severe congenital nemaline myopathy | Severe congenital nemaline myopathy (disorder)
+BMGC_DS19160,BMG_DS073073,1197156008,Intermediate nemaline myopathy,,,,,,,C5680452,,,MONDO:0015736,intermediate nemaline myopathy,Intermediate nemaline myopathy | Intermediate nemaline myopathy (disorder)
+BMGC_DS19161,BMG_DS073074,1197153000,Typical nemaline myopathy,,,,,,,C5680453,,,MONDO:0015737,typical nemaline myopathy,Typical nemaline myopathy | Typical nemaline myopathy (disorder)
+BMGC_DS19162,BMG_DS073080,,,,,,,,,C5680502,,,MONDO:0015802,autosomal dominant non-syndromic intellectual disability,
+BMGC_DS19163,BMG_DS073082,,,,,,,,,C5680504,,,MONDO:0015787,symptomatic form of hemophilia A in female carriers,
+BMGC_DS19164,BMG_DS073083,,,,,,,,,C5680505,,,MONDO:0015788,symptomatic form of hemophilia B in female carriers,
+BMGC_DS19165,BMG_DS073084,,,,,,,,,C5680507,,,MONDO:0015783,Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1,
+BMGC_DS19166,BMG_DS073085,,,,,,,,,C5680508,,,MONDO:0015784,Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2,
+BMGC_DS19167,BMG_DS073086,,,,,,,,,C5680509,,,MONDO:0015785,Prader-Willi syndrome due to translocation,
+BMGC_DS19168,BMG_DS073087,,,,,,,,,C5680510,,,MONDO:0015786,Prader-Willi syndrome due to imprinting mutation,
+BMGC_DS19169,BMG_DS073088,,,,,,,,,C5680513,,,MONDO:0015791,peripheral precocious puberty,
+BMGC_DS19170,BMG_DS073093,,,,,,,,,C5680524,,,MONDO:0016000,familial isolated hypoparathyroidism due to impaired PTH secretion,
+BMGC_DS19171,BMG_DS073094,,,,,,,,,C5680525,,,MONDO:0000508,syndromic intellectual disability,
+BMGC_DS19172,BMG_DS073096,,,,,,,,,C5680544,,,MONDO:0015962,inherited renal tubular disease,
+BMGC_DS19173,BMG_DS073097,,,,,,,,,C5680568,,,MONDO:0024237,inherited neurodegenerative disorder,
+BMGC_DS19174,BMG_DS073111,,,,,,,,,C5680648,,,MONDO:0015520,late infantile CACH syndrome,
+BMGC_DS19175,BMG_DS073112,,,,,,,,,C5680649,,,MONDO:0015521,juvenile or adult CACH syndrome,
+BMGC_DS19176,BMG_DS073113,,,,,,,,,C5680650,,,MONDO:0015519,congenital or early infantile CACH syndrome,
+BMGC_DS19177,BMG_DS073120,,,,,,,,,C5680682,,,MONDO:0015555,plaque-form urticaria pigmentosa,
+BMGC_DS19178,BMG_DS073121,,,,,,,,,C5680683,,,MONDO:0015554,typical urticaria pigmentosa,
+BMGC_DS19179,BMG_DS073122,,,,,,,,,C5680684,,,MONDO:0015556,nodular urticaria pigmentosa,
+BMGC_DS19180,BMG_DS073125,1264001009,De novo thrombotic microangiopathy following transplant of kidney,,,,,,,C5680696,,,,,De novo thrombotic microangiopathy after kidney transplantation | De novo thrombotic microangiopathy following transplant of kidney (disorder) | De novo thrombotic microangiopathy following transplant of kidney | De novo thrombotic microangiopathy after renal transplant
+BMGC_DS19181,BMG_DS073131,,,,,,,,,C5680720,,,MONDO:0016783,maternal 14q32.2 hypermethylation syndrome,
+BMGC_DS19182,BMG_DS073132,,,,,,,,,C5680721,,,MONDO:0016782,paternal 14q32.2 hypomethylation syndrome,
+BMGC_DS19183,BMG_DS073133,,,,,,,,,C5680724,,,MONDO:0016865,Kleefstra syndrome due to a point mutation,
+BMGC_DS19184,BMG_DS073138,1258972007,Baraitser Winter cerebrofrontofacial syndrome,,,,,,,C5680770,,,,,Baraitser Winter cerebrofrontofacial syndrome (disorder) | Baraitser Winter cerebrofrontofacial syndrome
+BMGC_DS19185,BMG_DS073143,,,,,,,,,C5680778,,,MONDO:0017111,isolated Dandy-Walker malformation without hydrocephalus,
+BMGC_DS19186,BMG_DS073144,,,,,,,,,C5680779,,,MONDO:0017110,isolated Dandy-Walker malformation with hydrocephalus,
+BMGC_DS19187,BMG_DS073147,1197747005,Autosomal semi-dominant severe lipodystrophic laminopathy,,,,,,,C5680783,,,MONDO:0017230,autosomal semi-dominant severe lipodystrophic laminopathy,Autosomal semi-dominant severe lipodystrophic laminopathy (disorder) | Autosomal semi-dominant severe lipodystrophic laminopathy
+BMGC_DS19188,BMG_DS073149,1237577000,Symptomatic form of Coffin-Lowry syndrome in female carrier,,,,,,,C5680787,,,MONDO:0017193,symptomatic form of Coffin-Lowry syndrome in female carriers,Symptomatic form of Coffin-Lowry syndrome in female carrier (disorder) | Symptomatic form of Coffin-Lowry syndrome in female carrier
+BMGC_DS19189,BMG_DS073152,,,,,,,,,C5680794,,,MONDO:0016112,hereditary inclusion-body myopathy,
+BMGC_DS19190,BMG_DS073156,,,,,,,,,C5680806,,,MONDO:0016144,qualitative or quantitative defects of delta-sarcoglycan,
+BMGC_DS19191,BMG_DS073158,,,,,,,,,C5680808,,,MONDO:0016141,qualitative or quantitative defects of alpha-sarcoglycan,
+BMGC_DS19192,BMG_DS073165,,,,,,,,,C5680831,,,MONDO:0016151,qualitative or quantitative defects of perlecan,
+BMGC_DS19193,BMG_DS073166,,,,,,,,,C5680832,,,MONDO:0016195,qualitative or quantitative defects of beta-myosin heavy chain (MYH7),
+BMGC_DS19194,BMG_DS073168,,,,,,,,,C5680835,,,MONDO:0016198,qualitative or quantitative defects of plectin,
+BMGC_DS19195,BMG_DS073183,,,,,,,,,C5680866,,,MONDO:0016306,"Niemann-Pick disease type C, severe perinatal form",
+BMGC_DS19196,BMG_DS073184,,,,,,,,,C5680867,,,MONDO:0016308,"Niemann-Pick disease type C, late infantile neurologic onset",
+BMGC_DS19197,BMG_DS073185,,,,,,,,,C5680868,,,MONDO:0016307,"Niemann-Pick disease type C, severe early infantile neurologic onset",
+BMGC_DS19198,BMG_DS073186,,,,,,,,,C5680869,,,MONDO:0016310,"Niemann-Pick disease type C, adult neurologic onset",
+BMGC_DS19199,BMG_DS073196,,,,,,,,,C5680916,,,MONDO:0016480,silver-Russell syndrome due to an imprinting defect of 11p15,
+BMGC_DS19200,BMG_DS073197,,,,,,,,,C5680917,,,MONDO:0016481,silver-Russell syndrome due to 11p15 microduplication,
+BMGC_DS19201,BMG_DS073198,,,,,,,,,C5680918,,,MONDO:0016476,Beckwith-Wiedemann syndrome due to CDKN1C mutation,
+BMGC_DS19202,BMG_DS073201,,,,,,,,,C5680922,,,MONDO:0016475,Beckwith-Wiedemann syndrome due to imprinting defect of 11p15,
+BMGC_DS19203,BMG_DS073205,,,,,,,,,C5680933,,,MONDO:0016547,Beckwith-Wiedemann syndrome due to NSD1 mutation,
+BMGC_DS19204,BMG_DS073210,,,,,,,,,C5680948,,,MONDO:0017973,non-classic congenital lipoid adrenal hyperplasia due to STAR deficency,
+BMGC_DS19205,BMG_DS073214,,,,,,,,,C5680967,,,MONDO:0017826,null pituitary adenoma,
+BMGC_DS19206,BMG_DS073216,,,,,,,,,C5680974,,,MONDO:0018217,Koolen-de Vries syndrome due to a point mutation,
+BMGC_DS19207,BMG_DS073217,,,,,,,,,C5680977,,,MONDO:0018240,TRPV4-related bone disorder,
+BMGC_DS19208,BMG_DS073218,,,,,,,,,C5680987,,,MONDO:0018161,non-hereditary retinoblastoma,
+BMGC_DS19209,BMG_DS073227,,,,,,,,,C5681013,,,MONDO:0017296,"glycerol kinase deficiency, adult form",
+BMGC_DS19210,BMG_DS073231,,,,,,,,,C5681029,,,MONDO:0017295,"glycerol kinase deficiency, juvenile form",
+BMGC_DS19211,BMG_DS073248,,,,,,,,,C5681074,,,MONDO:0017686,inborn aminoacylase deficiency,
+BMGC_DS19212,BMG_DS073250,,,,,,,,,C5681076,,,MONDO:0017737,intermediate severe Salla disease,
+BMGC_DS19213,BMG_DS073253,,,,,,,,,C5681089,,,MONDO:0017546,"congenital vertical talus, unilateral",
+BMGC_DS19214,BMG_DS073258,1208726006,Fever-associated acute infantile liver failure syndrome,,,,,,,C5681094,,,MONDO:0000023,infantile liver failure,Fever-associated acute infantile liver failure syndrome (disorder) | Fever-associated acute infantile liver failure syndrome
+BMGC_DS19215,BMG_DS073259,,,,,,,,,C5681095,,,MONDO:0018742,familial gastric type 1 neuroendocrine tumor,
+BMGC_DS19216,BMG_DS073265,1237344003,Symptomatic form of fragile X syndrome in female carrier,,,,,,,C5681104,,,MONDO:0018670,symptomatic form of fragile X syndrome in female carrier,Symptomatic form of fragile X syndrome in female carrier (disorder) | Symptomatic form of fragile X syndrome in female carrier
+BMGC_DS19217,BMG_DS073267,1260463008,Isolated focal non-epidermolytic palmoplantar keratoderma,,,,,,,C5681107,,,,,Isolated focal non-epidermolytic palmoplantar keratoderma (disorder) | Isolated focal non-epidermolytic palmoplantar keratoderma
+BMGC_DS19218,BMG_DS073268,1230005002,"Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome",,,,,,,C5681108,,618373,MONDO:0018657,pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome,"Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome (disorder) | Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome"
+BMGC_DS19219,BMG_DS073269,1254654006,"X-linked intellectual disability, hypotonia, movement disorder syndrome",,,,,,,C5681121,,,MONDO:0018709,X-linked intellectual disability-hypotonia-movement disorder syndrome,"X-linked intellectual disability, hypotonia, movement disorder syndrome | X-linked intellectual disability, hypotonia, movement disorder syndrome (disorder)"
+BMGC_DS19220,BMG_DS073270,1255335006,"X-linked intellectual disability, short stature, overweight syndrome",,,,,,,C5681122,,,,,"X-linked intellectual disability, short stature, overweight syndrome | X-linked intellectual disability, short stature, overweight syndrome (disorder)"
+BMGC_DS19221,BMG_DS073271,1260143005,"Megalencephaly, severe kyphoscoliosis, overgrowth syndrome",,,,,,,C5681123,,,MONDO:0018710,megalencephaly-severe kyphoscoliosis-overgrowth syndrome,"Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Megalencephaly, severe kyphoscoliosis, overgrowth syndrome (disorder)"
+BMGC_DS19222,BMG_DS073274,,,,,,,,,C5681129,,616708,MONDO:0014741,DeSanto-Shinawi syndrome due to WAC point mutation,
+BMGC_DS19223,BMG_DS073278,,,,,,,,,C5681146,,,MONDO:0018461,Angelman syndrome due to a point mutation,
+BMGC_DS19224,BMG_DS073280,1197586007,"Short stature, advanced bone age, early-onset osteoarthritis syndrome",,,,,,,C5681177,,,MONDO:0018566,short stature-advanced bone age-early-onset osteoarthritis syndrome,"Short stature, advanced bone age, early-onset osteoarthritis syndrome | Short stature, advanced bone age, early-onset osteoarthritis syndrome (disorder)"
+BMGC_DS19225,BMG_DS073281,1197588008,"X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome",,,,,,,C5681178,,,MONDO:0018569,X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome,"X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder) | X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome"
+BMGC_DS19226,BMG_DS073282,1197591008,"Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome",,,,,,,C5681179,,,MONDO:0018572,severe intellectual disability-hypotonia-strabismus-coarse face-planovalgus syndrome,"Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) | Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome"
+BMGC_DS19227,BMG_DS073283,1197592001,"Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome",,,,,,,C5681180,,,MONDO:0018573,intrauterine growth restriction-short stature-early adult-onset diabetes syndrome,"Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome | Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome (disorder)"
+BMGC_DS19228,BMG_DS073284,1220596009,"Microcephalic primordial dwarfism, insulin resistance syndrome",,,,,,,C5681181,,,,,"Microcephalic primordial dwarfism, insulin resistance syndrome (disorder) | Microcephalic primordial dwarfism, insulin resistance syndrome"
+BMGC_DS19229,BMG_DS073285,1197418004,"Familial atrial tachyarrhythmia, infra-Hisian cardiac conduction disease",,,,,,,C5681182,,,,,"Familial atrial tachyarrhythmia, infra-Hisian cardiac conduction disease | Familial atrial tachyarrhythmia, infra-Hisian cardiac conduction disease (disorder)"
+BMGC_DS19230,BMG_DS073286,1236843008,PDE4D haploinsufficiency syndrome,,,,,,,C5681186,,,,,PDE4D haploinsufficiency syndrome | Phosphodiesterase 4D haploinsufficiency syndrome (disorder) | Phosphodiesterase 4D haploinsufficiency syndrome
+BMGC_DS19231,BMG_DS073289,,,,,,,,,C5681190,,,MONDO:0018610,early-onset posterior subcapsular cataract,
+BMGC_DS19232,BMG_DS073290,,,,,,,,,C5681191,,,MONDO:0018611,early-onset lamellar cataract,
+BMGC_DS19233,BMG_DS073293,1237470001,"Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome",,,,,,,C5681197,,,,,"Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome | Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome (disorder)"
+BMGC_DS19234,BMG_DS073295,,,,,,,,,C5681199,,,MONDO:0018643,susceptibility to localized juvenile periodontitis,
+BMGC_DS19235,BMG_DS073297,,,,,,,,,C5681201,,,MONDO:0018655,hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome,
+BMGC_DS19236,BMG_DS073302,1279843003,Short rib polydactyly syndrome type 5,,,,,,,C5681240,,,,,Short rib polydactyly syndrome type 5 | Short rib polydactyly syndrome type V (disorder) | Short rib polydactyly syndrome type V
+BMGC_DS19237,BMG_DS073303,1237511005,EMILIN-1-related connective tissue disease,,,,,,,C5681244,,,MONDO:0044622,EMILIN-1-related connective tissue disease,Elastin microfibril interfacer 1 related connective tissue disease | EMILIN-1-related connective tissue disease | Elastin microfibril interfacer 1 related connective tissue disease (disorder)
+BMGC_DS19238,BMG_DS073304,,,,,,,,,C5681246,,,MONDO:0018839,acquired schizencephaly,
+BMGC_DS19239,BMG_DS073305,1220580006,Isolated neonatal sclerosing cholangitis,,,,,,,C5681248,,,,,Isolated neonatal sclerosing cholangitis (disorder) | Isolated neonatal sclerosing cholangitis
+BMGC_DS19240,BMG_DS073307,,,,,,,,,C5681257,,,MONDO:0018795,syndromic constitutional thrombocytopenia,
+BMGC_DS19241,BMG_DS073309,1269236003,"Primary hypomagnesemia, refractory seizures, intellectual disability syndrome",,,,,,,C5681271,,,,,"Primary hypomagnesemia, refractory seizures, intellectual disability syndrome | Primary hypomagnesemia, refractory seizures, intellectual disability syndrome (disorder) | Primary hypomagnesaemia, refractory seizures, intellectual disability syndrome"
+BMGC_DS19242,BMG_DS073327,,,,,,,,,C5681306,,,MONDO:0019119,muscular channelopathy,
+BMGC_DS19243,BMG_DS073328,,,,,,,,,C5681310,,,MONDO:0019042,multiple congenital anomalies/dysmorphic syndrome,
+BMGC_DS19244,BMG_DS073331,1256081007,Pustular pyoderma gangrenosum,,,,,,,C5681317,,,MONDO:0035236,pustular pyoderma gangrenosum,Pustular pyoderma gangrenosum (disorder) | Pustular pyoderma gangrenosum
+BMGC_DS19245,BMG_DS073333,1222655009,"Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome",,,,,,,C5681321,,,MONDO:0034092,optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome,"Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (disorder) | Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome"
+BMGC_DS19246,BMG_DS073334,1269271003,"Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome",,,,,,,C5681324,,,MONDO:0034110,atypical Fanconi syndrome-neonatal hyperinsulinism syndrome,"Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome (disorder) | Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome"
+BMGC_DS19247,BMG_DS073337,,,,,,,,,C5681331,,,MONDO:0001713,inherited aplastic anemia,
+BMGC_DS19248,BMG_DS073338,1222661007,"Early-onset calcifying leukoencephalopathy, skeletal dysplasia",,,,,,,C5681333,,,MONDO:0034143,early-onset calcifying leukoencephalopathy-skeletal dysplasia,"Early-onset calcifying leucoencephalopathy, skeletal dysplasia | Early-onset calcifying leukoencephalopathy, skeletal dysplasia | Early-onset calcifying leukoencephalopathy, skeletal dysplasia (disorder)"
+BMGC_DS19249,BMG_DS073339,1222660008,"Pancreatic agenesis, holoprosencephaly syndrome",,,,,,,C5681334,,,MONDO:0034142,pancreatic agenesis-holoprosencephaly syndrome,"Pancreatic agenesis, holoprosencephaly syndrome | Pancreatic agenesis, holoprosencephaly syndrome (disorder)"
+BMGC_DS19250,BMG_DS073340,1255323007,"Spastic ataxia, dysarthria due to glutaminase deficiency",,,,,,,C5681336,,,MONDO:0034146,spastic ataxia-dysarthria due to glutaminase deficiency,"Spastic ataxia, dysarthria due to glutaminase deficiency (disorder) | Spastic ataxia, dysarthria due to glutaminase deficiency"
+BMGC_DS19251,BMG_DS073347,,,,,,,,,C5681365,,,MONDO:0019530,non-syndromic syndactyly,
+BMGC_DS19252,BMG_DS073348,,,,,,,,,C5681367,,,MONDO:0957048,isolated macular dystrophy,
+BMGC_DS19253,BMG_DS073354,1217370006,LAMA5-related multisystemic syndrome,,,,,,,C5681442,,,MONDO:0033856,LAMA5-related multisystemic syndrome,LAMA5-related multisystemic syndrome | Laminin subunit alpha 5-related multisystemic syndrome | Laminin subunit alpha 5-related multisystemic syndrome (disorder)
+BMGC_DS19254,BMG_DS073355,1279889005,"Microcephaly, facial dysmorphism, ocular anomalies, multiple congenital anomalies syndrome",,,,,,,C5681443,,,MONDO:0035027,microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome,"Microcephaly, facial dysmorphism, ocular anomalies, multiple congenital anomalies syndrome (disorder) | Microcephaly, facial dysmorphism, ocular anomalies, multiple congenital anomalies syndrome"
+BMGC_DS19255,BMG_DS073356,1260140008,"Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome",,,,,,,C5681444,,,MONDO:0033853,congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome,"Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome (disorder)"
+BMGC_DS19256,BMG_DS073358,1217373008,"Diaphragmatic hernia, short bowel, asplenia syndrome",,,,,,,C5681454,,,MONDO:0035105,diaphragmatic hernia-short bowel-asplenia syndrome,"Diaphragmatic hernia, short bowel, asplenia syndrome (disorder) | Diaphragmatic hernia, short bowel, asplenia syndrome"
+BMGC_DS19257,BMG_DS073361,1236807002,Encephalopathy due to mitochondrial and peroxisomal fission defect,,,,,,,C5681458,,,MONDO:0054865,encephalopathy due to mitochondrial and peroxisomal fission defect,Encephalopathy due to mitochondrial and peroxisomal fission defect (disorder) | Encephalopathy due to mitochondrial and peroxisomal fission defect
+BMGC_DS19258,BMG_DS073366,1231281009,"46,XY disorder of sex development due to isolated 17,20-lyase deficiency",,,,,,,C5681470,,,,,"46,XY disorder of sex development due to isolated 17,20-lyase deficiency (disorder) | 46,XY disorder of sex development due to isolated 17,20-lyase deficiency"
+BMGC_DS19259,BMG_DS073367,,,,,,,,,C5681477,,,MONDO:0019284,inherited isolated nail anomaly,
+BMGC_DS19260,BMG_DS073379,,,,,,,,,C5681523,,,MONDO:0020071,infantile epilepsy syndrome,
+BMGC_DS19261,BMG_DS073382,,,,,,,,,C5681526,,,MONDO:0020072,childhood-onset epilepsy syndrome,
+BMGC_DS19262,BMG_DS073383,1332384001,"CCNK-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome",,,,,,,C5681527,,,MONDO:0035775,CCNK-related neurodevelopmental disorder-severe intellectual disability-facial dysmorphism syndrome,"Cyclin K-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome | CCNK-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome | Cyclin K-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome (disorder)"
+BMGC_DS19263,BMG_DS073384,1300131002,"NRXN1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance",,,,,,,C5681528,,,MONDO:0035774,NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance,"Neurexin 1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance | Neurexin 1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance (disorder) | NRXN1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance | NRXN1(neurexin 1) related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance"
+BMGC_DS19264,BMG_DS073387,,,,,,,,,C5681536,,267430,MONDO:0009970,renal tubular dysgenesis of genetic origin,
+BMGC_DS19265,BMG_DS073398,1303273003,"IRF2BPL-related regressive neurodevelopmental disorder, dystonia, seizures syndrome",,,,,,,C5681583,,,,,"Interferon regulatory factor 2 binding protein like-related regressive neurodevelopmental disorder, dystonia, seizures syndrome | IRF2BPL-related regressive neurodevelopmental disorder, dystonia, seizures syndrome | Interferon regulatory factor 2 binding protein like-related regressive neurodevelopmental disorder, dystonia, seizures syndrome (disorder)"
+BMGC_DS19266,BMG_DS073400,1300119004,"SETD2-related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome",,,,,,,C5681587,,,MONDO:0035706,SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome,"SET domain containing 2, histone lysine methyltransferase-related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome (disorder) | SETD2 (SET domain containing 2, histone lysine methyltransferase) related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome | SET domain containing 2, histone lysine methyltransferase-related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome | SETD2-related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome"
+BMGC_DS19267,BMG_DS073402,,,,,,,,,C5681589,,,MONDO:0035713,FOXG1 syndrome due to intragenic alteration,
+BMGC_DS19268,BMG_DS073403,,,,,,,,,C5681598,,,MONDO:0019681,juvenile sialidosis type 2,
+BMGC_DS19269,BMG_DS073404,,,,,,,,,C5681599,,,MONDO:0019682,congenital sialidosis type 2,
+BMGC_DS19270,BMG_DS073405,,,,,,,,,C5681601,,,MONDO:0035734,hereditary angioedema with normal C1inh not related to F12 or PLG variant,
+BMGC_DS19271,BMG_DS073406,,,,,,,,,C5681604,,,MONDO:0019685,FGFR3-related chondrodysplasia,
+BMGC_DS19272,BMG_DS073408,,,,,,,,,C5681613,,,MONDO:0019769,"X-linked intellectual disability, Sutherland-Haan type",
+BMGC_DS19273,BMG_DS073409,,,,,,,,,C5681614,,,MONDO:0019768,"X-linked intellectual disability, Golabi-Ito-hall type",
+BMGC_DS19274,BMG_DS073410,,,,,,,,,C5681615,,,MONDO:0019767,hamel cerebro-palato-cardiac syndrome,
+BMGC_DS19275,BMG_DS073411,,,,,,,,,C5681616,,,MONDO:0019766,"X-linked intellectual disability, Porteous type",
+BMGC_DS19276,BMG_DS073412,,,,,,,,,C5681620,,,MONDO:0019742,late-onset nephronophthisis,
+BMGC_DS19277,BMG_DS073416,1260095004,Menke Hennekam syndrome,,,,,,,C5681632,,,MONDO:0020774,Menke-Hennekam syndrome,Menke Hennekam syndrome | Menke Hennekam syndrome (disorder)
+BMGC_DS19278,BMG_DS073417,1208998007,"TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome",,,,,,,C5681633,,,MONDO:0035661,TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome,"Tumor necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome | TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome | Tumour necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome | Tumor necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome (disorder)"
+BMGC_DS19279,BMG_DS073419,1260195002,"GRIN2B-related developmental delay, intellectual disability, autism spectrum disorder",,,,,,,C5681638,,,MONDO:0035122,"GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder","GRIN2B-related developmental delay, intellectual disability, autism spectrum disorder | Glutamate ionotropic receptor NMDA type subunit 2B-related developmental delay, intellectual disability, autism spectrum disorder (disorder) | Glutamate ionotropic receptor NMDA type subunit 2B-related developmental delay, intellectual disability, autism spectrum disorder"
+BMGC_DS19280,BMG_DS073423,,,,,,,,,C5681644,,,MONDO:0020376,early-onset nuclear cataract,
+BMGC_DS19281,BMG_DS073428,,,,,,,,,C5681679,,,MONDO:0020297,Noonan syndrome and Noonan-related syndrome,
+BMGC_DS19282,BMG_DS073442,,,,,,,,,C5681733,,,MONDO:0020127,hereditary peripheral neuropathy,
+BMGC_DS19283,BMG_DS073443,,,,,,,,,C5681739,,,MONDO:0015191,myopathic intestinal pseudoobstruction,
+BMGC_DS19284,BMG_DS073448,,,,,,,,,C5681803,,,MONDO:0015096,familial hypofibrinogenemia,
+BMGC_DS19285,BMG_DS073456,,,,,,,,,C5681819,,,MONDO:0036217,lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to a point mutation,
+BMGC_DS19286,BMG_DS073459,,,,,,,,,C5681825,,,MONDO:0850088,EGF-related primary hypomagnesemia with intellectual disability,
+BMGC_DS19287,BMG_DS073460,,,,,,,,,C5681826,,,MONDO:0850087,primary hypomagnesemia-generalized seizures-intellectual disability-obesity syndrome,
+BMGC_DS19288,BMG_DS073461,,,,,,,,,C5681829,,,MONDO:0850053,F12-associated cold autoinflammatory syndrome,
+BMGC_DS19289,BMG_DS073462,1340174002,"Developmental delay, immunodeficiency, leukoencephalopathy, hypohomocysteinemia syndrome",,,,,,,C5681830,,,MONDO:0850071,developmental delay-immunodeficiency-leukoencephalopathy-hypohomocysteinemia syndrome,"Developmental delay, immunodeficiency, leukoencephalopathy, hypohomocysteinemia syndrome | Developmental delay, immunodeficiency, leukoencephalopathy, hypohomocysteinemia syndrome (disorder) | Developmental delay, immunodeficiency, leucoencephalopathy, hypohomocysteinemia syndrome"
+BMGC_DS19290,BMG_DS073464,,,,,,,,,C5681834,,,MONDO:0018462,Angelman syndrome due to imprinting defect in 15q11-q13,
+BMGC_DS19291,BMG_DS073465,,,,,,,,,C5681844,,,MONDO:0019220,inborn disorder of cobalamin metabolism and transport,
+BMGC_DS19292,BMG_DS073467,1222668001,CELSR1-related late-onset primary lymphedema,,,,,,,C5681848,,,MONDO:0035499,CELSR1-related late-onset primary lymphedema,Cadherin EGF LAG seven-pass G-type receptor 1-related late-onset primary lymphedema (disorder) | Cadherin EGF LAG seven-pass G-type receptor 1-related late-onset primary lymphedema | Cadherin EGF LAG seven-pass G-type receptor 1-related late-onset primary lymphoedema | CELSR1-related late-onset primary lymphedema | CELSR1-related late-onset primary lymphoedema
+BMGC_DS19293,BMG_DS073530,1197524007,Autosomal recessive amyotrophic lateral sclerosis type 1,,,,,,,C5686324,,,,,Autosomal recessive amyotrophic lateral sclerosis type 1 | Autosomal recessive amyotrophic lateral sclerosis type 1 (disorder) | ALS1 AR - amyotrophic lateral sclerosis type 1 autosomal recessive | Autosomal recessive ALS (amyotrophic lateral sclerosis) type 1
+BMGC_DS19294,BMG_DS073876,1217228004,"X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome",,,,,,,C5687848,,,MONDO:0018724,X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome,"X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome | X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome (disorder)"
+BMGC_DS19295,BMG_DS073916,1217704000,Chronic antibiotic-refractory pouchitis,,,,,,,C5688196,,,,,Chronic antibiotic-refractory ileal pouchitis (disorder) | Chronic antibiotic-refractory ileal pouchitis | CARP - chronic antibiotic-refractory pouchitis | Chronic antibiotic-refractory pouchitis
+BMGC_DS19296,BMG_DS073917,1220590003,Familial chilblain lupus erythematosus,,,,,,,C5688224,,,MONDO:0018827,familial chilblain lupus,Familial chilblain lupus erythematosus (disorder) | Familial chilblain lupus erythematosus
+BMGC_DS19297,BMG_DS073918,1220598005,Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy,,,,,,,C5688227,,,MONDO:0018576,non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy,Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy (disorder) | Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy | Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy
+BMGC_DS19298,BMG_DS073963,1229876001,Lethal brain and heart developmental defects syndrome,,,,,,,C5688452,,,,,Lethal brain and heart developmental defects syndrome (disorder) | Lethal brain and heart developmental defects syndrome
+BMGC_DS19299,BMG_DS074056,,Chronic Kidney Diseases of Uncertain Etiology,Chronic Kidney Diseases of Uncertain Etiology,,,,,,C5690757,D000092702,,,,
+BMGC_DS19300,BMG_DS074061,,Perinatal Cytomegalovirus Infection,Cytomegalovirus Infections,,,,,,C5690863,D003586,,,,
+BMGC_DS19301,BMG_DS074062,,Childhood Idiopathic Nephrotic Syndrome,Nephrotic Syndrome,,,,,,C5690874,D009404,,,,
+BMGC_DS19302,BMG_DS074063,,Complement 3 Glomerulopathies,"Glomerulonephritis, Membranoproliferative",,,,,,C5690882,D015432,,,,
+BMGC_DS19303,BMG_DS074087,,Varicose Bronchiectasis,Bronchiectasis,,,,,,C5691384,D001987,,,,
+BMGC_DS19304,BMG_DS074088,,Major Adverse Cardiac Events,Cardiovascular Diseases,,,,,,C5691385,D002318,,,,
+BMGC_DS19305,BMG_DS074091,,Dental Enamel Erosion,Tooth Erosion,,,,,,C5691421,D014077,,,,
+BMGC_DS19306,BMG_DS074094,,"cardiomyopathy, dilated, 1b",,,,,,,C5700078,C536231,600884,MONDO:0010951,dilated cardiomyopathy 1B,
+BMGC_DS19307,BMG_DS074096,,Acid Maltase Deficiency,Glycogen Storage Disease Type II,,,,,,C5700101,D006009,,,,
+BMGC_DS19308,BMG_DS074097,1254890002,Localized non-Herlitz junctional epidermolysis bullosa,,,,,,,C5700116,,,MONDO:0016673,"localized junctional epidermolysis bullosa, non-Herlitz type",Localised non-Herlitz junctional epidermolysis bullosa | Localized junctional epidermolysis bullosa non-Herlitz type (disorder) | Localized non-Herlitz junctional epidermolysis bullosa | Localised junctional epidermolysis bullosa non-Herlitz type | Localized junctional epidermolysis bullosa non-Herlitz type
+BMGC_DS19309,BMG_DS074098,711406009,Autosomal recessive axonal neuropathy with neuromyotonia,,,,,,,C5700127,,137200,MONDO:0007646,Gamstorp-Wohlfart syndrome,"Autosomal recessive axonal neuropathy with neuromyotonia | Autosomal recessive neuromyotonia with axonal neuropathy | Autosomal recessive axonal neuropathy with neuromyotonia (disorder) | Myokymia, myotonia and muscle wasting | Gamstorp-Wohlfart syndrome"
+BMGC_DS19310,BMG_DS074103,1237512003,"Short stature, developmental delay, congenital heart defect syndrome",,,,,,,C5700245,,617044,MONDO:0014881,transketolase deficiency,"Short stature, developmental delay, congenital heart defect syndrome | Short stature, developmental delay, congenital heart defect syndrome (disorder) | TKT (transketolase) deficiency"
+BMGC_DS19311,BMG_DS074107,,"Segawa syndrome, autosomal recessive",,,,,,,C5700309,C537537,,MONDO:0100064,tyrosine hydroxylase deficiency,
+BMGC_DS19312,BMG_DS074108,,"MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 1",,,,,,,C5700310,,252011;600857,MONDO:0100294,"mitochondrial complex II deficiency, nuclear type 1",
+BMGC_DS19313,BMG_DS074110,,"PARKINSONISM-DYSTONIA 1, INFANTILE-ONSET",,,,,,,C5700336,,613135,MONDO:0054835,classic dopamine transporter deficiency syndrome,
+BMGC_DS19314,BMG_DS074112,,Carnosinase Deficiency,,,,,DOID:0060177,homocarnosinosis,C5700357,C535328,,,,
+BMGC_DS19315,BMG_DS074113,1237338002,Exercise-induced malignant hyperthermia,,,,,,,C5700399,,,MONDO:0018752,exercise-induced malignant hyperthermia,Exercise-induced malignant hyperthermia (disorder) | Exercise-induced malignant hyperthermia
+BMGC_DS19316,BMG_DS074116,,"Platyspondylic Lethal Skeletal Dysplasia, Luton Type",,,,,,,C5703068,C563627,,,,
+BMGC_DS19317,BMG_DS074117,,,,,,,,,C5703292,,620121,MONDO:0859316,"iron overload, susceptibility to",
+BMGC_DS19318,BMG_DS074118,1259242002,Hereditary von Willebrand disease,,,,,,,C5703318,,,MONDO:0019565,hereditary von Willebrand disease,Hereditary von Willebrand disease | Hereditary von Willebrand disease (disorder)
+BMGC_DS19319,BMG_DS074121,,NSAID-Exacerbated Respiratory Disease,"Asthma, Aspirin-Induced",,,,,,C5704570,D055963,,,,
+BMGC_DS19320,BMG_DS074407,1240462005,Generalized inflammatory peeling skin syndrome,,,,,DOID:0070520,peeling skin syndrome 1,C5768235,,,,,Generalized inflammatory peeling skin syndrome | Generalised inflammatory peeling skin syndrome | Generalized inflammatory peeling skin syndrome (disorder)
+BMGC_DS19321,BMG_DS074640,,CARDIAC VALVULAR DYSPLASIA 1,,,,,DOID:0080633,developmental cardiac valvular defect,C5774175,,212093;602382,MONDO:0008913,"cardiac valvular defect, developmental",
+BMGC_DS19322,BMG_DS074641,,"PSEUDOHYPOALDOSTERONISM, TYPE IB1, AUTOSOMAL RECESSIVE",,,,,,,C5774176,,264350;600228,MONDO:0009917,"pseudohypoaldosteronism, type IB1, autosomal recessive",
+BMGC_DS19323,BMG_DS074642,,"EPILEPSY, X-LINKED 1, WITH VARIABLE LEARNING DISABILITIES AND BEHAVIOR DISORDERS",,,,,,,C5774177,,300491;313440,MONDO:0010339,"epilepsy, X-linked 1, with variable learning disabilities and behavior disorders",
+BMGC_DS19324,BMG_DS074643,,"EPILEPSY, X-LINKED 2, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT AND DYSMORPHIC FEATURES",,,,,,,C5774178,,305660;301091,MONDO:0859564,"epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features",
+BMGC_DS19325,BMG_DS074644,,HIJAZI-REIS SYNDROME,,,,,,,C5774179,,301094;300237,MONDO:0859085,"neurodevelopmental disorder with gait disturbance, dysmorphic facies, and behavioral abnormalities, X-linked",
+BMGC_DS19326,BMG_DS074645,,,,,,,,,C5774180,,301095,MONDO:0859086,"intellectual developmental disorder, X-linked 110",
+BMGC_DS19327,BMG_DS074646,,"MICROPHTHALMIA, SYNDROMIC 16",,,,,,,C5774181,,601881;611038,MONDO:0012604,isolated microphthalmia 3,
+BMGC_DS19328,BMG_DS074647,,"SPASTIC PARAPLEGIA 87, AUTOSOMAL RECESSIVE",,,,,DOID:0070456,hereditary spastic paraplegia 87,C5774182,,619953;619966,MONDO:0031019,"spastic paraplegia 87, autosomal recessive",
+BMGC_DS19329,BMG_DS074648,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 104,,,,,DOID:0070390,developmental and epileptic encephalopathy 104,C5774183,,192130;619970,MONDO:0031021,developmental and epileptic encephalopathy 104,
+BMGC_DS19330,BMG_DS074649,,NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND BRAIN ATROPHY,,,,,,,C5774184,,619971;192130,MONDO:0859265,neurodevelopmental disorder with epilepsy and brain atrophy,
+BMGC_DS19331,BMG_DS074650,,"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT, ABSENT LANGUAGE, CEREBRAL HYPOMYELINATION, AND BRAIN ATROPHY",,,,,,,C5774185,,609514;619972,MONDO:0859266,"neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy",
+BMGC_DS19332,BMG_DS074651,,TUMOR PREDISPOSITION SYNDROME 2,,,,,,,C5774186,,603574;619975,MONDO:0859267,tumor predisposition syndrome 2,
+BMGC_DS19333,BMG_DS074652,,"MACULAR DYSTROPHY, RETINAL, 4",,,,,DOID:0070441,retinal macular dystrophy 4,C5774187,,187520;619977,MONDO:0859568,"macular dystrophy, retinal, 4",
+BMGC_DS19334,BMG_DS074653,,BRADDOCK-CAREY SYNDROME 1,,,,,,,C5774188,,619980,MONDO:0859569,Braddock-Carey syndrome 1,
+BMGC_DS19335,BMG_DS074654,,BRADDOCK-CAREY SYNDROME 2,,,,,,,C5774189,,619981;617569,MONDO:0859570,braddock-carey syndrome 2,
+BMGC_DS19336,BMG_DS074655,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 105 WITH HYPOPITUITARISM,,,,,DOID:0070391,developmental and epileptic encephalopathy 105,C5774190,,605752;619983,MONDO:0031028,developmental and epileptic encephalopathy 105 with hypopituitarism,
+BMGC_DS19337,BMG_DS074656,,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 25,,,,,,,C5774191,,619979;619985,MONDO:0859271,glycosylphosphatidylinositol biosynthesis defect 25,
+BMGC_DS19338,BMG_DS074657,,"IMMUNODEFICIENCY 107, SUSCEPTIBILITY TO INVASIVE STAPHYLOCOCCUS AUREUS INFECTION",,,,,,,C5774192,,615712;619986,MONDO:0031030,"immunodeficiency 107, susceptibility to invasive staphylococcus aureus infection",
+BMGC_DS19339,BMG_DS074658,,,,,,,,,C5774193,,619988,MONDO:0031031,"intellectual developmental disorder, autosomal recessive 77",
+BMGC_DS19340,BMG_DS074659,,NEURODEVELOPMENTAL DISORDER WITH SPEECH DELAY AND VARIABLE OCULAR ANOMALIES,,,,,,,C5774194,,619989;616662,MONDO:0859272,neurodevelopmental disorder with speech delay and variable ocular anomalies,
+BMGC_DS19341,BMG_DS074660,,"LIVER DISEASE, SEVERE CONGENITAL",,,,,,,C5774195,,614606;619991,MONDO:0859273,"liver disease, severe congenital",
+BMGC_DS19342,BMG_DS074661,,"NEURODEVELOPMENTAL DISORDER WITH INTENTION TREMOR, PYRAMIDAL SIGNS, DYSPRAXIA, AND OCULAR ANOMALIES",,,,,,,C5774196,,613176;619995,MONDO:0859274,"neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies",
+BMGC_DS19343,BMG_DS074662,,"NEURODEVELOPMENTAL DISORDER WITH SPASTICITY, SEIZURES, AND BRAIN ABNORMALITIES",,,,,,,C5774197,,616173;620001,MONDO:0859275,"neurodevelopmental disorder with spasticity, seizures, and brain abnormalities",
+BMGC_DS19344,BMG_DS074663,,PRIMORDIAL DWARFISM-IMMUNODEFICIENCY-LIPODYSTROPHY SYNDROME,,,,,,,C5774198,,176635;620005,MONDO:0859276,primordial dwarfism-immunodeficiency-lipodystrophy syndrome,
+BMGC_DS19345,BMG_DS074664,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH MUSCLE TONE ABNORMALITIES AND DISTAL SKELETAL DEFECTS,,,,,,,C5774199,,620007;608302,MONDO:0859277,intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects,
+BMGC_DS19346,BMG_DS074665,,"KERATODERMA-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL RECESSIVE",,,,,,,C5774200,,608552;620009,MONDO:0859278,"keratoderma-ichthyosis-deafness syndrome, autosomal recessive",
+BMGC_DS19347,BMG_DS074666,,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL RECESSIVE 6",,,,,DOID:0081425,autosomal recessive distal hereditary motor neuronopathy 6,C5774201,,609139;620011,MONDO:0859279,"spinal muscular atrophy, distal, autosomal recessive, 6",
+BMGC_DS19348,BMG_DS074667,,"DEVELOPMENTAL DELAY, HYPOTONIA, AND IMPAIRED LANGUAGE",,,,,DOID:0070420,"developmental delay, hypotonia, and impaired language",C5774202,,620012;606278,MONDO:0859280,"developmental delay, hypotonia, and impaired language",
+BMGC_DS19349,BMG_DS074668,,LYMPHATIC MALFORMATION 12,,,,,,,C5774203,,620014;614511,MONDO:0031043,lymphatic malformation 12,
+BMGC_DS19350,BMG_DS074669,,"ADVANCE SLEEP PHASE SYNDROME, FAMILIAL, 4",,,,,DOID:0061006,advanced sleep phase syndrome 4,C5774204,,620015,MONDO:0031044,"advance sleep phase syndrome, familial, 4",
+BMGC_DS19351,BMG_DS074670,,"ARTHROGRYPOSIS, DISTAL, TYPE 11",,,,,,,C5774205,,164860;620019,MONDO:0031045,"arthrogryposis, distal, IIa 11",
+BMGC_DS19352,BMG_DS074671,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND DYSMORPHIC FACIES,,,,,,,C5774206,,614235;620021,MONDO:0859281,intellectual developmental disorder with autism and dysmorphic facies,
+BMGC_DS19353,BMG_DS074672,,"STICKLER SYNDROME, TYPE VI",,,,,,,C5774207,,120270;620022,MONDO:0031047,"stickler syndrome, IIa 6",
+BMGC_DS19354,BMG_DS074673,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, MOVEMENT ABNORMALITIES, AND SEIZURES",,,,,,,C5774208,,118491;620023,MONDO:0859282,"neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures",
+BMGC_DS19355,BMG_DS074674,,"NEURODEVELOPMENTAL DISORDER WITH SEIZURES, MICROCEPHALY, AND BRAIN ABNORMALITIES",,,,,,,C5774209,,620024;603141,MONDO:0859283,"neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities",
+BMGC_DS19356,BMG_DS074675,,"DIAPHRAGMATIC HERNIA 4, WITH CARDIOVASCULAR DEFECTS",,,,,,,C5774210,,603687;620025,MONDO:0859571,"diaphragmatic hernia 4, with cardiovascular defects",
+BMGC_DS19357,BMG_DS074676,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SHORT STATURE, AND SPEECH DELAY",,,,,,,C5774211,,602103;620027,MONDO:0859285,"neurodevelopmental disorder with microcephaly, short stature, and speech delay",
+BMGC_DS19358,BMG_DS074677,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 106,,,,,DOID:0070392,developmental and epileptic encephalopathy 106,C5774212,,611482;620028,MONDO:0031052,developmental and epileptic encephalopathy 106,
+BMGC_DS19359,BMG_DS074678,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, LANGUAGE DELAY, AND SKELETAL DEFECTS WITH OR WITHOUT SEIZURES",,,,,DOID:0070536,"neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures",C5774213,,620029,MONDO:0859286,"neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures",
+BMGC_DS19360,BMG_DS074679,,"CILIARY DYSKINESIA, PRIMARY, 48, WITHOUT SITUS INVERSUS",,,,,,,C5774214,,620032;603575,MONDO:0031054,"ciliary dyskinesia, primary, 48, without situs inversus",
+BMGC_DS19361,BMG_DS074680,,,,,,,,,C5774215,,620033,MONDO:0031055,developmental and epileptic encephalopathy 107,
+BMGC_DS19362,BMG_DS074681,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND ABSENT LANGUAGE",,,,,,,C5774216,,602017;620038,MONDO:0859287,"neurodevelopmental disorder with microcephaly, hypotonia, and absent language",
+BMGC_DS19363,BMG_DS074682,,"DYSKERATOSIS CONGENITA, DIGENIC",,,,,DOID:0060984,digenic dyskeratosis congenita,C5774217,,188350;620040,MONDO:0031057,"dyskeratosis congenita, digenic",
+BMGC_DS19364,BMG_DS074683,,BONE MARROW FAILURE AND DIABETES MELLITUS SYNDROME,,,,,,,C5774218,,601266;620044,MONDO:0859288,bone marrow failure and diabetes mellitus syndrome,
+BMGC_DS19365,BMG_DS074684,,INTESTINAL DYSMOTILITY SYNDROME,,,,,,,C5774219,,620045;610108,MONDO:0859289,intestinal dysmotility syndrome,
+BMGC_DS19366,BMG_DS074685,,"MICROCEPHALY 29, PRIMARY, AUTOSOMAL RECESSIVE",,,,,,,C5774220,,608074;620047,MONDO:0031060,"microcephaly 29, primary, autosomal recessive",
+BMGC_DS19367,BMG_DS074686,,"NEPHROTIC SYNDROME, TYPE 26",,,,,,,C5774221,,601033;620049,MONDO:0031061,"nephrotic syndrome, IIa 26",
+BMGC_DS19368,BMG_DS074687,,POLYCYSTIC KIDNEY DISEASE 7,,,,,DOID:0060952,polycystic kidney disease 7,C5774222,,604565;620056,MONDO:0031062,polycystic kidney disease 7,
+BMGC_DS19369,BMG_DS074688,,"DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FACIAL FEATURES, AND SPARSE HAIR 2",,,,,DOID:0070478,diphthamide deficiency syndrome 2,C5774223,,620062;603456,MONDO:0100217,"developmental delay with short stature, dysmorphic facial features, and sparse hair 2",
+BMGC_DS19370,BMG_DS074689,,"DEVELOPMENTAL DELAY, BEHAVIORAL ABNORMALITIES, AND NEUROPSYCHIATRIC DISORDERS",,,,,,,C5774224,,616416;620065,MONDO:0859292,"developmental delay, behavioral abnormalities, and neuropsychiatric disorders",
+BMGC_DS19371,BMG_DS074690,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CEREBRAL ATROPHY, AND VISUAL IMPAIRMENT",,,,,,,C5774225,,611262;620066,MONDO:0859293,"neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment",
+BMGC_DS19372,BMG_DS074691,,CARDIAC VALVULAR DYSPLASIA 2,,,,,,,C5774226,,607513;620067,MONDO:0859572,cardiac valvular dysplasia 2,
+BMGC_DS19373,BMG_DS074692,,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2II",,,,,,,C5774227,,620068;604878,MONDO:0031068,"Charcot-Marie-Tooth disease, axonal, IIa 2II",
+BMGC_DS19374,BMG_DS074693,,"NEURODEVELOPMENTAL DISORDER WITH SHORT STATURE, PROMINENT FOREHEAD, AND FEEDING DIFFICULTIES",,,,,DOID:0070479,"neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties",C5774228,,620070;611075,MONDO:0859295,"neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties",
+BMGC_DS19375,BMG_DS074694,,BIRK-AHARONI SYNDROME,,,,,DOID:0081324,"neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss",C5774229,,602706;620071,MONDO:0859296,"neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss",
+BMGC_DS19376,BMG_DS074695,,DIAMOND-BLACKFAN ANEMIA 21,,,,,,,C5774230,,614951;620072,MONDO:0031071,Diamond-Blackfan anemia 21,
+BMGC_DS19377,BMG_DS074696,,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND SKELETAL AND BRAIN ABNORMALITIES,,,,,,,C5774231,,607201;620073,MONDO:0859297,neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities,
+BMGC_DS19378,BMG_DS074697,,"NEURODEVELOPMENTAL DISORDER WITH FACIAL DYSMORPHISM, ABSENT LANGUAGE, AND PSEUDO-PELGER-HUET ANOMALY",,,,,,,C5774232,,620075;613585,MONDO:0859298,"neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-pelger-huet anomaly",
+BMGC_DS19379,BMG_DS074698,,BENT BONE DYSPLASIA SYNDROME 2,,,,,DOID:0060993,bent bone dysplasia syndrome 2,C5774233,,601033;620076,MONDO:0859573,bent bone dysplasia syndrome 2,
+BMGC_DS19380,BMG_DS074699,,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 10",,,,,DOID:0081399,autosomal dominant distal hereditary motor neuronopathy 10,C5774234,,130660;620080,MONDO:0859300,"neuronopathy, distal hereditary motor, autosomal dominant 10",
+BMGC_DS19381,BMG_DS074700,,NEURODEVELOPMENTAL DISORDER WITH CRANIOFACIAL DYSMORPHISM AND SKELETAL DEFECTS,,,,,,,C5774235,,620083;601035,MONDO:0859301,neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects,
+BMGC_DS19382,BMG_DS074701,,SPERMATOGENIC FAILURE 76,,,,,DOID:0070575,spermatogenic failure 76,C5774236,,620084;612324,MONDO:0031077,spermatogenic failure 76,
+BMGC_DS19383,BMG_DS074702,,HYPERMETABOLISM DUE TO UNCOUPLED MITOCHONDRIAL OXIDATIVE PHOSPHORYLATION 2,,,,,,,C5774237,,102910;620085,MONDO:0859302,hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2,
+BMGC_DS19384,BMG_DS074703,,INTELLECTUAL DEVELOPMENTAL DISORDER WITH OCULAR ANOMALIES AND DISTINCTIVE FACIAL FEATURES,,,,,DOID:0081301,intellectual developmental disorder with ocular anomalies and distinctive facial features,C5774238,,616951;620086,MONDO:0859303,intellectual developmental disorder with ocular anomalies and distinctive facial features,
+BMGC_DS19385,BMG_DS074704,,"NEURODEGENERATION, CHILDHOOD-ONSET, WITH MULTISYSTEM INVOLVEMENT DUE TO MITOCHONDRIAL DYSFUNCTION",,,,,,,C5774240,,604407;620089,MONDO:0859304,"neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction",
+BMGC_DS19386,BMG_DS074705,,NEURODEVELOPMENTAL DISORDER WITH EYE MOVEMENT ABNORMALITIES AND ATAXIA,,,,,DOID:0081275,neurodevelopmental disorder with eye movement abnormalities and ataxia,C5774241,,616309;620094,MONDO:0859305,neurodevelopmental disorder with eye movement abnormalities and ataxia,
+BMGC_DS19387,BMG_DS074706,,DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL DISABILITY AND DYSMORPHIC FACIES,,,,,,,C5774242,,601594;620098,MONDO:0859306,developmental delay with variable intellectual disability and dysmorphic facies,
+BMGC_DS19388,BMG_DS074707,,CLEIDOCRANIAL DYSPLASIA 2,,,,,,,C5774243,,121360;620099,MONDO:0859307,cleidocranial dysplasia 2,
+BMGC_DS19389,BMG_DS074708,,RETINITIS PIGMENTOSA 95,,,,,,,C5774244,,620102;610362,MONDO:0859308,retinitis pigmentosa 95,
+BMGC_DS19390,BMG_DS074709,,SPERMATOGENIC FAILURE 77,,,,,DOID:0070576,spermatogenic failure 77,C5774245,,620103;604839,MONDO:0031083,spermatogenic failure 77,
+BMGC_DS19391,BMG_DS074710,,"AMELOGENESIS IMPERFECTA, TYPE IK",,,,,DOID:0060945,amelogenesis imperfecta type 1K,C5774246,,620104,MONDO:0031084,"amelogenesis imperfecta, IIa 1K",
+BMGC_DS19392,BMG_DS074711,,"SPASTIC PARAPLEGIA 88, AUTOSOMAL DOMINANT",,,,,DOID:0070457,hereditary spastic paraplegia 88,C5774247,,620106;601892,MONDO:0859309,"spastic paraplegia 88, autosomal dominant",
+BMGC_DS19393,BMG_DS074712,,OROFACIODIGITAL SYNDROME XIX,,,,,DOID:0060960,orofaciodigital syndrome XIX,C5774248,,608095;620107,MONDO:0859310,orofaciodigital syndrome 19,
+BMGC_DS19394,BMG_DS074713,,"CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1J",,,,,,,C5774249,,147267;620111,MONDO:0859311,"Charcot-Marie-Tooth disease, demyelinating, type 1J",
+BMGC_DS19395,BMG_DS074714,,"NEURODEVELOPMENTAL DISORDER WITH GROWTH RETARDATION, DYSMORPHIC FACIES, AND CORPUS CALLOSUM ABNORMALITIES",,,,,,,C5774251,,608866;620113,MONDO:0859312,"neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities",
+BMGC_DS19396,BMG_DS074715,,NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND WITH OR WITHOUT SEIZURES,,,,,,,C5774252,,620114;608230,MONDO:0859313,neurodevelopmental disorder with speech impairment and with or without seizures,
+BMGC_DS19397,BMG_DS074716,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 108,,,,,DOID:0070394,developmental and epileptic encephalopathy 108,C5774253,,612258;620115,MONDO:0859314,developmental and epileptic encephalopathy 108,
+BMGC_DS19398,BMG_DS074717,,"PSEUDOHYPOALDOSTERONISM, TYPE IB2, AUTOSOMAL RECESSIVE",,,,,,,C5774255,,600760;620125,MONDO:0859317,"pseudohypoaldosteronism, type IB2, autosomal recessive",
+BMGC_DS19399,BMG_DS074718,,"PSEUDOHYPOALDOSTERONISM, TYPE IB3, AUTOSOMAL RECESSIVE",,,,,,,C5774256,,600761;620126,MONDO:0859318,"pseudohypoaldosteronism, type IB3, autosomal recessive",
+BMGC_DS19400,BMG_DS074719,,"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 8",,,,,,,C5774257,,620133;609683,MONDO:0859319,"dyskeratosis congenita, autosomal recessive 8",
+BMGC_DS19401,BMG_DS074720,,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 39",,,,,,,C5774258,,620135;603842,MONDO:0859320,"mitochondrial complex I deficiency, nuclear type 39",
+BMGC_DS19402,BMG_DS074721,,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 11",,,,,,,C5774259,,613844;620137,MONDO:0859321,"mitochondrial complex 3 deficiency, nuclear type 11",
+BMGC_DS19403,BMG_DS074722,,"MYOPATHY WITH MYALGIA, INCREASED SERUM CREATINE KINASE, AND WITH OR WITHOUT EPISODIC RHABDOMYOLYSIS",,,,,,,C5774260,,620138,MONDO:0859322,"myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis",
+BMGC_DS19404,BMG_DS074723,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 56,,,,,DOID:0070429,combined oxidative phosphorylation deficiency 56,C5774261,,614948;620139,MONDO:0859323,combined oxidative phosphorylation deficiency 56,
+BMGC_DS19405,BMG_DS074724,,"DEVELOPMENTAL DELAY, LANGUAGE IMPAIRMENT, AND OCULAR ABNORMALITIES",,,,,,,C5774262,,604226;620141,MONDO:0859324,"developmental delay, language impairment, and ocular abnormalities",
+BMGC_DS19406,BMG_DS074725,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 109,,,,,DOID:0070378,developmental and epileptic encephalopathy 109,C5774263,,620145;603619,MONDO:0859325,developmental and epileptic encephalopathy 109,
+BMGC_DS19407,BMG_DS074726,,"ICHTHYOSIS, ANNULAR EPIDERMOLYTIC, 2",,,,,,,C5774264,,139350;620148,MONDO:0859574,"ichthyosis, annular epidermolytic, 2",
+BMGC_DS19408,BMG_DS074727,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 110,,,,,DOID:0070395,developmental and epileptic encephalopathy 110,C5774265,,114204;620149,MONDO:0859327,developmental and epileptic encephalopathy 110,
+BMGC_DS19409,BMG_DS074728,,"HYPOMAGNESEMIA 7, RENAL, WITH OR WITHOUT DILATED CARDIOMYOPATHY",,,,,DOID:0060972,"renal hypomagnesemia 7, with or without dilated cardiomyopathy",C5774266,,620152;608268,MONDO:0859328,"hypomagnesemia 7, renal, with or without dilated cardiomyopathy",
+BMGC_DS19410,BMG_DS074729,,MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 4,,,,,DOID:0060981,mosaic variegated aneuploidy syndrome 4,C5774267,,620153;620142,MONDO:0859329,mosaic variegated aneuploidy syndrome 4,
+BMGC_DS19411,BMG_DS074730,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 13,,,,,,,C5774268,,612053;620154,MONDO:0859330,oocyte maturation defect 13,
+BMGC_DS19412,BMG_DS074731,,RABIN-PAPPAS SYNDROME,,,,,,,C5774269,,612778;620155,MONDO:0859331,Rabin-Pappas syndrome,
+BMGC_DS19413,BMG_DS074732,,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 11",,,,,,,C5774270,,613231;620156,MONDO:0859332,"cortical dysplasia, complex, with other brain malformations 11",
+BMGC_DS19414,BMG_DS074733,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 70",,,,,,,C5774271,,620157;612778,MONDO:0859333,"intellectual developmental disorder, autosomal dominant 70",
+BMGC_DS19415,BMG_DS074734,,SPINOCEREBELLAR ATAXIA 50,,,,,,,C5774272,,602367;620158,MONDO:0859334,spinocerebellar ataxia 50,
+BMGC_DS19416,BMG_DS074735,,CONGENITAL MYOPATHY 15,,,,,DOID:0081347,congenital myopathy 15,C5774273,,191039;620161,MONDO:0859335,congenital myopathy 15,
+BMGC_DS19417,BMG_DS074736,,"MUSCULAR DYSTROPHY, CONGENITAL, WITH OR WITHOUT SEIZURES",,,,,,,C5774274,,620166;604027,MONDO:0859336,"muscular dystrophy, congenital, with or without seizures",
+BMGC_DS19418,BMG_DS074737,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 57,,,,,DOID:0070430,combined oxidative phosphorylation deficiency 57,C5774275,,620167;608188,MONDO:0859337,combined oxidative phosphorylation deficiency 57,
+BMGC_DS19419,BMG_DS074738,,SPERMATOGENIC FAILURE 78,,,,,DOID:0070577,spermatogenic failure 78,C5774276,,620160;620170,MONDO:0859338,spermatogenic failure 78,
+BMGC_DS19420,BMG_DS074739,,"TOOTH AGENESIS, SELECTIVE, 10",,,,,,,C5774277,,612920;620173,MONDO:0859339,"tooth agenesis, selective, 10",
+BMGC_DS19421,BMG_DS074740,,"SPINOCEREBELLAR ATAXIA 27B, LATE-ONSET",,,,,,,C5774278,,601515;620174,MONDO:0859340,"spinocerebellar ataxia 27B, late-onset",
+BMGC_DS19422,BMG_DS074741,,HYPOTRICHOSIS 15,,,,,DOID:0060968,hypotrichosis 15,C5774279,,620177;611956,MONDO:0859341,hypotrichosis 15,
+BMGC_DS19423,BMG_DS074742,,"MICROCEPHALY 30, PRIMARY, AUTOSOMAL RECESSIVE",,,,,,,C5774280,,602452;620183,MONDO:0859342,"microcephaly 30, primary, autosomal recessive",
+BMGC_DS19424,BMG_DS074743,,ATELIS SYNDROME 1,,,,,,,C5774281,,610348;620184,MONDO:0859575,Atelis syndrome 1,
+BMGC_DS19425,BMG_DS074744,,ATELIS SYNDROME 2,,,,,,,C5774282,,609386;620185,MONDO:0859576,Atelis syndrome 2,
+BMGC_DS19426,BMG_DS074745,,"BRANCHIAL ARCH ABNORMALITIES, CHOANAL ATRESIA, ATHELIA, HEARING LOSS, AND HYPOTHYROIDISM SYNDROME",,,,,,,C5774283,,620186;602113,MONDO:0859345,"obsolete branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome",
+BMGC_DS19427,BMG_DS074746,,MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 7 WITH INFLAMMATION AND TUMOR PREDISPOSITION,,,,,DOID:0060982,mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition,C5774284,,620189;602686,MONDO:0859346,mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition,
+BMGC_DS19428,BMG_DS074747,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, DYSMORPHIC FACIES, AND SKIN ABNORMALITIES",,,,,,,C5774285,,611610;620191,MONDO:0859347,"neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities",
+BMGC_DS19429,BMG_DS074748,,LACRIMOAURICULODENTODIGITAL SYNDROME 2,,,,,DOID:0081371,lacrimoauriculodentodigital syndrome 2,C5774286,,620192,MONDO:0859577,lacrimoauriculodentodigital syndrome 2,
+BMGC_DS19430,BMG_DS074749,,LACRIMOAURICULODENTODIGITAL SYNDROME 3,,,,,DOID:0081372,lacrimoauriculodentodigital syndrome 3,C5774287,,620193,MONDO:0859578,lacrimoauriculodentodigital syndrome 3,
+BMGC_DS19431,BMG_DS074750,,"NEURODEVELOPMENTAL DISORDER WITH POOR GROWTH, LARGE EARS, AND DYSMORPHIC FACIES",,,,,,,C5774288,,617103;620194,MONDO:0859350,"neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies",
+BMGC_DS19432,BMG_DS074751,,OBESITY AND HYPOPIGMENTATION,,,,,,,C5774289,,620195,MONDO:0859351,obesity and hypopigmentation,
+BMGC_DS19433,BMG_DS074752,,SPERMATOGENIC FAILURE 79,,,,,DOID:0070578,spermatogenic failure 79,C5774290,,615215;620196,MONDO:0859352,spermatogenic failure 79,
+BMGC_DS19434,BMG_DS074753,,"CILIARY DYSKINESIA, PRIMARY, 49, WITHOUT SITUS INVERSUS",,,,,,,C5774291,,620197;620187,MONDO:0859353,"ciliary dyskinesia, primary, 49, without situs inversus",
+BMGC_DS19435,BMG_DS074754,,"THYROID HORMONE METABOLISM, ABNORMAL, 3",,,,,,,C5774292,,165060;620198,MONDO:0859354,"thyroid hormone metabolism, abnormal, 3",
+BMGC_DS19436,BMG_DS074755,,INFLAMMATORY POIKILODERMA WITH HAIR ABNORMALITIES AND ACRAL KERATOSES,,,,,DOID:0070510,inflammatory poikiloderma with hair abnormalities and acral keratoses,C5774293,,620199,MONDO:0859355,inflammatory poikiloderma with hair abnormalities and acral keratoses,
+BMGC_DS19437,BMG_DS074756,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIy",,,,,,,C5774294,,612056;620200,MONDO:0859356,"congenital disorder of glycosylation, type IIy",
+BMGC_DS19438,BMG_DS074757,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIz",,,,,,,C5774295,,601118;620201,MONDO:0859357,"congenital disorder of glycosylation, type IIz",
+BMGC_DS19439,BMG_DS074758,,"CARDIOMYOPATHY, DILATED, 2H",,,,,,,C5774296,,620203;601913,MONDO:0859358,"cardiomyopathy, dilated, 2H",
+BMGC_DS19440,BMG_DS074759,,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 33",,,,,DOID:0070414,autosomal recessive spinocerebellar ataxia 33,C5774297,,620208;620204,MONDO:0859360,"spinocerebellar ataxia, autosomal recessive 33",
+BMGC_DS19441,BMG_DS074760,,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND ISCHIOPUBIC HYPOPLASIA,,,,,,,C5774298,,603385;620210,MONDO:0859361,neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia,
+BMGC_DS19442,BMG_DS074761,,"HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 8",,,,,DOID:0081328,familial hyperinsulinemic hypoglycemia 8,C5774299,,616149;620211,MONDO:0859362,"hyperinsulinemic hypoglycemia, familial, 8",
+BMGC_DS19443,BMG_DS074762,,"SPASTIC PARAPLEGIA 79A, AUTOSOMAL DOMINANT, WITH ATAXIA",,,,,DOID:0070455,hereditary spastic paraplegia 79A,C5774300,,191342;620221,MONDO:0859363,"spastic paraplegia 79A, autosomal dominant, with ataxia",
+BMGC_DS19444,BMG_DS074763,,SPERMATOGENIC FAILURE 80,,,,,DOID:0070579,spermatogenic failure 80,C5774301,,620222;615288,MONDO:0859364,spermatogenic failure 80,
+BMGC_DS19445,BMG_DS074764,,"DEAFNESS, AUTOSOMAL DOMINANT 85",,,,,DOID:0070605,autosomal dominant nonsyndromic deafness 85,C5774302,,617445;620227,MONDO:0859366,"hearing loss, autosomal dominant 85",
+BMGC_DS19446,BMG_DS074765,,RETINITIS PIGMENTOSA 96,,,,,,,C5774303,,181031;620228,MONDO:0859367,retinitis pigmentosa 96,
+BMGC_DS19447,BMG_DS074766,,SHORT QT SYNDROME 7,,,,,,,C5774304,,620231;106195,MONDO:0859368,short QT syndrome 7,
+BMGC_DS19448,BMG_DS074767,,"JOINT CONTRACTURES, OSTEOCHONDROMAS, AND B-CELL LYMPHOMA",,,,,,,C5774305,,620232;600490,MONDO:0859369,"joint contractures, osteochondromas, and B-cell lymphoma",
+BMGC_DS19449,BMG_DS074768,,"RESPIRATORY INFECTIONS, RECURRENT, AND FAILURE TO THRIVE WITH OR WITHOUT DIARRHEA",,,,,,,C5774306,,606358;620233,MONDO:0859370,"respiratory infections, recurrent, and failure to thrive with or without diarrhea",
+BMGC_DS19450,BMG_DS074769,,,,,,,,,C5774307,,620235,MONDO:0859371,"rhabdomyolysis, susceptibility to, 1",
+BMGC_DS19451,BMG_DS074770,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 29, WITH POLYGLUCOSAN BODIES",,,,,,,C5774308,,611295;620236,MONDO:0859372,"cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies",
+BMGC_DS19452,BMG_DS074771,,"DEAFNESS, AUTOSOMAL RECESSIVE 120",,,,,,,C5774309,,620215;620238,MONDO:0859374,"hearing loss, autosomal recessive 120",
+BMGC_DS19453,BMG_DS074772,,TESSADORI-BICKNELL-VAN HAAFTEN NEURODEVELOPMENTAL SYNDROME 3,,,,,,,C5774310,,602830;619950,MONDO:0030993,Tessadori-Van Haaften neurodevelopmental syndrome 3,
+BMGC_DS19454,BMG_DS074773,,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 12",,,,,,,C5774311,,620010;608552,MONDO:0031040,"cholestasis, progressive familial intrahepatic, 12",
+BMGC_DS19455,BMG_DS074774,,"CLEIDOCRANIAL DYSPLASIA 1, FORME FRUSTE, WITH BRACHYDACTYLY",,,,,,,C5774312,,119600;600211,,,
+BMGC_DS19456,BMG_DS074775,,"CLEIDOCRANIAL DYSPLASIA 1, FORME FRUSTE, DENTAL ANOMALIES ONLY",,,,,,,C5774315,,119600;600211,,,
+BMGC_DS19457,BMG_DS074776,,MEDULLOBLASTOMA PREDISPOSITION SYNDROME,,,,,,,C5774316,,155255;612250,,,
+BMGC_DS19458,BMG_DS074777,,FAMILIAL APOLIPOPROTEIN GENE CLUSTER DELETION SYNDROME,,,,,,,C5774318,,620058,MONDO:0859290,familial apolipoprotein gene cluster deletion syndrome,
+BMGC_DS19459,BMG_DS074780,,LADD SYNDROME 1,,,,,,,C5774323,,149730;176943,MONDO:0100302,LADD syndrome 1,
+BMGC_DS19460,BMG_DS074819,230318005,Genetic torsion dystonia,,8A02.0Z,"Primary dystonia, unspecified",G24.1,DOID:0090039;DOID:0090034;DOID:0060730;DOID:0090046;DOID:0090041;DOID:0090037;DOID:0090050;DOID:0090055;DOID:0090042;DOID:0090043;DOID:0090057;DOID:0090038,dystonia 27 | dystonia 21 | torsion dystonia 1 | dopa-responsive dystonia | torsion dystonia 2 | torsion dystonia 4 | torsion dystonia 13 | myoclonic dystonia 11 | dystonia 25 | X-linked dystonia-parkinsonism | torsion dystonia 6 | torsion dystonia 17,C5779546,,,,,Idiopathic familial dystonia | Idiopathic familial dystonia (disorder) | Genetic torsion dystonia
+BMGC_DS19461,BMG_DS074821,,,,,,,,,C5779548,,,MONDO:0019587,autosomal dominant nonsyndromic hearing loss,
+BMGC_DS19462,BMG_DS074823,1231183003,Familial isolated retinal arterial tortuosity,,,,,,,C5779553,,,,,Familial isolated retinal arterial tortuosity (disorder) | Familial isolated retinal arterial tortuosity | Retinal hemorrhage with vascular tortuosity | Tortuosity of retinal arteries | Retinal haemorrhage with vascular tortuosity | Retinal arteriolar tortuosity
+BMGC_DS19463,BMG_DS074826,416780008,"Primary degenerative dementia of the Alzheimer type, presenile onset",,,,,,,C5779573,,,,,"Primary degenerative dementia of the Alzheimer type, presenile onset (disorder) | Primary degenerative dementia of the Alzheimer type, presenile onset | Primary degenerative dementia of the Alzheimer type, early onset | Dementia in Alzheimer's disease with early onset | Dementia of the Alzheimers type with early onset | Presenile dementia, Alzheimer's type | Alzheimer's disease with early onset | Dementia in Alzheimer's disease - type 2"
+BMGC_DS19464,BMG_DS074829,203040006;111246005;205402004,Arthrogryposis multiplex congenita,,LD26.41,Arthrogryposis multiplex congenita,Q74.3,,,C5779613,,MTHU009867,MONDO:0015168,arthrogryposis multiplex congenita,Arthrogryposis (& [multiplex congenita]) | Arthrogryposis | Arthrogryposis multiplex congenita | Arthrogryposis multiplex congenita. | Arthrogryposis (& [multiplex congenita]) (disorder) | Arthrogryposis | Arthrogryposis (disorder) | Arthrogryposis multiplex congenita | Arthrogryposis multiplex congenita (disorder) | Multiple congenital arthrogryposis | AMC - arthrogryposis multiplex congenita
+BMGC_DS19465,BMG_DS074831,,RETINITIS PIGMENTOSA-DEAFNESS SYNDROME,,,,,,,C5779620,,500004,MONDO:0010775,retinitis pigmentosa-deafness syndrome,
+BMGC_DS19466,BMG_DS074832,1279836009,Familial multinodular goiter syndrome,,,,,,,C5779622,,,,,Familial multinodular goiter syndrome (disorder) | Familial multinodular goiter syndrome | FMNG - familial multinodular goitre | Familial multinodular goiter | Familial multinodular goitre | FMNG - familial multinodular goiter | Familial multinodular goitre syndrome
+BMGC_DS19467,BMG_DS074834,271807003,Eruption of skin (disorder),,,,,,,C5779629,,,,,Eruption | Skin rash | Skin eruption | Rash | Breaking out - eruption | Exanthem | Eruption of skin (disorder) | Eruption of skin
+BMGC_DS19468,BMG_DS074836,,"NEPHROLITHIASIS, CALCIUM OXALATE, 1",,,,,DOID:0080652,calcium oxalate nephrolithiasis,C5779632,,167030;610130,MONDO:0020722,nephrolithiasis susceptibility caused by SLC26A1,
+BMGC_DS19469,BMG_DS074837,238091006,Lecithin cholesterol acyltransferase deficiency,,,,,,,C5779633,,,MONDO:0018999,LCAT deficiency,Lecithin cholesterol acyltransferase deficiency | Lecithin cholesterol acyltransferase deficiency (disorder) | LCAT (lecithin-cholesterol acyltransferase) deficiency | LCAT deficiency
+BMGC_DS19470,BMG_DS074838,,,,,,,,,C5779636,,,MONDO:0018208,neurofibromatosis type 1 due to NF1 mutation or intragenic deletion,
+BMGC_DS19471,BMG_DS074840,,"RIBOFLAVIN TRANSPORTER DEFICIENCY, TYPE 1",,,,,,,C5779638,,615026,MONDO:0004573,ariboflavinosis,
+BMGC_DS19472,BMG_DS074841,,"Liver Failure, Fulminant","Liver Failure, Acute",,,,,,C5779644,D017114,,,,
+BMGC_DS19473,BMG_DS074845,23502006;48982009,Bannwarth syndrome,,,,,,,C5779706,,,,,Lyme disease | Steere's disease | Lyme borreliosis | Lyme disease (disorder) | Bannwarth syndrome | Tick-borne meningopolyneuritis | Bannwarth syndrome (disorder) | Garin-Bujadoux-Bannwarth syndrome
+BMGC_DS19474,BMG_DS074846,716996008,L1 syndrome,,,,,,,C5779710,,,MONDO:0017140,L1 syndrome,"Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome | L1 syndrome | CRASH syndrome | Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome (disorder) | Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome"
+BMGC_DS19475,BMG_DS074847,,,,,,,,,C5779711,,,MONDO:0017630,X-linked complicated spastic paraplegia type 1,
+BMGC_DS19476,BMG_DS074850,,CARPAL TUNNEL SYNDROME 1,,,,,DOID:0070466,carpal tunnel syndrome 1,C5779776,,115430,MONDO:0020730,carpal tunnel syndrome 1,
+BMGC_DS19477,BMG_DS074856,1264009006,Isolated cytochrome C oxidase deficiency,,,,,DOID:0081377,"COX deficiency, benign infantile mitochondrial myopathy",C5779825,,,,,Isolated cytochrome C oxidase deficiency (disorder) | Isolated COX (cytochrome C oxidase) deficiency | Isolated mitochondrial respiratory chain complex IV deficiency | Isolated cytochrome C oxidase deficiency
+BMGC_DS19478,BMG_DS074857,,"USHER SYNDROME, TYPE IIIA",,,,,,,C5779850,,276902;606397,MONDO:0010170,Usher syndrome type 3A,
+BMGC_DS19479,BMG_DS074860,,MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1,,,,,,,C5779875,,604004;605908,MONDO:0024555,megalencephalic leukoencephalopathy with subcortical cysts 1,
+BMGC_DS19480,BMG_DS074861,,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1,,,,,DOID:0060213,frontotemporal dementia and/or amyotrophic lateral sclerosis 1,C5779877,,614260;105550,MONDO:0007105,frontotemporal dementia and/or amyotrophic lateral sclerosis 1,
+BMGC_DS19481,BMG_DS074862,719950001,Triphalangeal thumb and polysyndactyly syndrome,,,,,,,C5779878,,190605,MONDO:0017454,triphalangeal thumb-polysyndactyly syndrome,Triphalangeal thumb and polysyndactyly syndrome (disorder) | Triphalangeal thumb and polysyndactyly syndrome
+BMGC_DS19482,BMG_DS074866,,COMPLEMENT COMPONENT 4B DEFICIENCY,,,,,,,C5779962,,614379,,,
+BMGC_DS19483,BMG_DS074867,1275631007,Developmental and epileptic encephalopathy,,,,G93.45,,,C5779964,,,,,DEE - developmental and epileptic encephalopathy | Developmental and epileptic encephalopathy | Developmental and epileptic encephalopathy (disorder)
+BMGC_DS19484,BMG_DS074870,,LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER 1,,,,,DOID:0070374,leukoencephalopathy with vanishing white matter 1,C5779972,,603896;606686,MONDO:0020507,leukoencephalopathy with vanishing white matter 1,
+BMGC_DS19485,BMG_DS074871,,LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER 5,,,,,DOID:0070367,leukoencephalopathy with vanishing white matter 5,C5779973,,603945;620315,MONDO:0957873,leukoencephalopathy with vanishing white matter 5,
+BMGC_DS19486,BMG_DS074873,1260450002,"Infantile multisystem neurologic, endocrine, pancreatic disease",,,,,,,C5779989,,,,,"IMNEPD - infantile multisystem neurologic, endocrine, pancreatic disease | Infantile multisystem neurologic, endocrine, pancreatic disease (disorder) | Infantile multisystem neurologic, endocrine, pancreatic disease"
+BMGC_DS19487,BMG_DS074874,1279837000,Congenital cataract microcornea with corneal opacity,,,,,,,C5779991,,,,,Congenital cataract microcornea with corneal opacity | CCMCO - congenital cataract microcornea with corneal opacity | Congenital cataract microcornea with corneal opacity (disorder)
+BMGC_DS19488,BMG_DS074875,,HOUGE-JANSSENS SYNDROME 1,,,,,DOID:0070065,autosomal dominant intellectual developmental disorder 35,C5779996,,616355,MONDO:0014602,Hogue-Janssens syndrome 1,
+BMGC_DS19489,BMG_DS074876,1269224009,"Craniosynostosis, microretrognathia, severe intellectual disability syndrome",,,,,,,C5780021,,,,,"Craniosynostosis, microretrognathia, severe intellectual disability syndrome | Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder)"
+BMGC_DS19490,BMG_DS074877,,,,,,,,,C5780022,,158600,MONDO:0008026,autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures,
+BMGC_DS19491,BMG_DS074879,1269233006,"Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome",,,,,,,C5780029,,,,,"Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome | Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome (disorder)"
+BMGC_DS19492,BMG_DS074884,,Classic Refsum Disease,Refsum Disease,,,,,,C5780941,D012035,,,,
+BMGC_DS19493,BMG_DS074885,,Adult Refsum Disease,Refsum Disease,,,,,,C5781059,D012035,,,,
+BMGC_DS19494,BMG_DS074887,,Hereditary Motor And Sensory Neuropathy IV,Refsum Disease,,,,,,C5781118,D012035,,,,
+BMGC_DS19495,BMG_DS074893,,,,,,,,,C5781610,,620444,MONDO:0958194,craniofacial microsomia 2,
+BMGC_DS19496,BMG_DS074895,,EPIDERMOLYTIC HYPERKERATOSIS 1,,,,,DOID:0081358,epidermolytic hyperkeratosis 1,C5781874,,113800;139350,MONDO:0700249,epidermolytic hyperkeratosis 1,
+BMGC_DS19497,BMG_DS074896,,Phytanic Acid Oxidase Deficiency,Refsum Disease,,,,,,C5781943,D012035,,,,
+BMGC_DS19498,BMG_DS074899,,Heredopathia Atactica Polyneuritiformis,Refsum Disease,,,,,,C5782141,D012035,,,,
+BMGC_DS19499,BMG_DS075112,,,,,,,,,C5816698,,,MONDO:0958353,intermediate collagen VI-related muscular dystrophy,
+BMGC_DS19500,BMG_DS075113,1299154002,"CDK13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome",,,,,,,C5816700,,,,,"Cyclin dependent kinase 13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome (disorder) | CDK13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome | Cyclin dependent kinase 13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome | CDK13-related disorder"
+BMGC_DS19501,BMG_DS075144,,,,,,,,,C5816734,,616863,MONDO:0958071,Hao-Fountain syndrome due to USP7 mutation,
+BMGC_DS19502,BMG_DS075145,1303865002,"Marfanoid habitus, facial dysmorphism, skeletal abnormality, heart defect syndrome",,,,,,,C5816735,,,,,"Marfanoid habitus, facial dysmorphism, skeletal abnormality, heart defect syndrome | Marfanoid habitus, facial dysmorphism, skeletal abnormality, heart defect syndrome (disorder)"
+BMGC_DS19503,BMG_DS075151,1299153008,Digenic hemochromatosis,,,,,,,C5816744,,,MONDO:0958085,digenic hemochromatosis,Digenic haemochromatosis | Digenic hemochromatosis (disorder) | Digenic hemochromatosis
+BMGC_DS19504,BMG_DS075154,1340041000,Combined immunodeficiency due to FCHO1 deficiency,,,,,,,C5816748,,,,,Combined immunodeficiency due to FCHO1 deficiency | Combined immunodeficiency due to FCH and mu domain containing endocytic adaptor 1 deficiency | Combined immunodeficiency due to FCH and mu domain containing endocytic adaptor 1 deficiency (disorder)
+BMGC_DS19505,BMG_DS075155,1303910000,SLC40A1-related hemochromatosis,,,,,,,C5816749,,,,,Solute carrier family 40 member 1-related hemochromatosis (disorder) | SLC40A1-related haemochromatosis | Solute carrier family 40 member 1-related hemochromatosis | Solute carrier family 40 member 1-related haemochromatosis | SLC40A1-related hemochromatosis
+BMGC_DS19506,BMG_DS075156,,,,,,,DOID:0060280,primary pigmented nodular adrenocortical disease,C5816750,,,MONDO:0958262,isolated primary pigmented nodular adrenocortical disease,
+BMGC_DS19507,BMG_DS075157,,,,,,,,,C5816752,,,MONDO:0957473,craniosynostosis-facial dysmorphism-chiari-1 malformation-developmental and language delay syndrome,
+BMGC_DS19508,BMG_DS075158,1303866001,"MYT1L-related developmental delay, intellectual disability, obesity syndrome",,,,,,,C5816753,,,MONDO:0957477,MYT1L-related developmental delay-intellectual disability-obesity syndrome,"Myelin transcription factor 1 like-related developmental delay, intellectual disability, obesity syndrome (disorder) | MYT1L-related Prader-Willi-like syndrome | MYT1L-related developmental delay, intellectual disability, obesity syndrome | Myelin transcription factor 1 like-related developmental delay, intellectual disability, obesity syndrome"
+BMGC_DS19509,BMG_DS075163,,,,,,,,,C5816761,,,MONDO:0968990,genetic central precocious puberty in male,
+BMGC_DS19510,BMG_DS075166,,,,,,,,,C5816765,,,MONDO:0958354,genetic central precocious puberty in female,
+BMGC_DS19511,BMG_DS075173,1300198006,"SMARCA2-related blepharophimosis, intellectual disability syndrome",,,,,,,C5816784,,,,,"SMARCA2-related blepharophimosis, intellectual disability syndrome | SMARCA2 (SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A, member 2) related blepharophimosis, intellectual disability syndrome | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A, member 2-related blepharophimosis, intellectual disability syndrome | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A, member 2-related blepharophimosis, intellectual disability syndrome (disorder)"
+BMGC_DS19512,BMG_DS075177,,,,,,,DOID:0070627,B-lymphoblastic leukemia with TCF3-HLF fusion,C5816789,,,MONDO:0957428,B-lymphoblastic leukemia/lymphoma with t(17;19),
+BMGC_DS19513,BMG_DS075178,,,,,,,,,C5816790,,,MONDO:0957427,B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2),
+BMGC_DS19514,BMG_DS075179,1303585005,"Infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome",,,,,,,C5816791,,,,,"HPDL-related Leigh-like encephalopathy | Infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome | Infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome (disorder) | HPDL-related infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome | HPDL (4-hydroxyphenylpyruvate dioxygenase like) related infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome"
+BMGC_DS19515,BMG_DS075180,1303586006,"Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome",,,,,,,C5816792,,,,,"Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome | Cerebellar ataxia, brain abnormalities, cardiac conduction defects syndrome | Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome (disorder) | Neurodevelopmental delay, hypotonia, cerebellar atrophy, cardiac conduction defects syndrome"
+BMGC_DS19516,BMG_DS075183,,,,,,,,,C5816796,,,MONDO:0957443,autosomal recessive ataxia due to PEX2 deficiency,
+BMGC_DS19517,BMG_DS075184,,,,,,,,,C5816797,,,MONDO:0957442,autosomal recessive ataxia due to PEX16 deficiency,
+BMGC_DS19518,BMG_DS075186,1303280001,PUM1-related cerebellar ataxia,,,,,,,C5816800,,,,,Pumilio RNA binding family member 1-related cerebellar ataxia (disorder) | PUM1-related cerebellar ataxia | Pumilio RNA binding family member 1-related cerebellar ataxia | Adult-onset spinocerebellar ataxia type 47 | Adult-onset SCA47 (spinocerebellar ataxia type 47)
+BMGC_DS19519,BMG_DS075187,1304276001,CHD8 overgrowth syndrome,,,,,,,C5816801,,,,,"CHD8-related intellectual disability, autism, macrocephaly, tall stature syndrome | Chromodomain helicase DNA binding protein 8 overgrowth syndrome | CHD8 overgrowth syndrome | Chromodomain helicase DNA binding protein 8 overgrowth syndrome (disorder)"
+BMGC_DS19520,BMG_DS075188,,,,,,,,,C5816803,,,MONDO:0858998,mesomelic dysplasia-digital anomalies-intellectual disability syndrome,
+BMGC_DS19521,BMG_DS075746,,Autonomic Central Nervous System Diseases,Autonomic Nervous System Diseases,,,,,,C5828508,D001342,,,,
+BMGC_DS19522,BMG_DS075747,,Non-Familial Dysautonomia,Autonomic Nervous System Diseases,,,,,,C5828509,D001342,,,,
+BMGC_DS19523,BMG_DS075749,,Mandibulofacial Dysostosis (MFD1),Mandibulofacial Dysostosis,,,,,,C5828530,D008342,,MONDO:0015483,mandibulofacial dysostosis,
+BMGC_DS19524,BMG_DS075750,,Kunjin virus Infection,West Nile Fever,,,,,,C5828557,D014901,,,,
+BMGC_DS19525,BMG_DS075753,,Septic Cavernous Sinusitis,Cavernous Sinus Thrombosis,,,,,,C5828565,D020226,,,,
+BMGC_DS19526,BMG_DS075754,,Acute Regional Pain Syndrome,Complex Regional Pain Syndromes,,,,,,C5828566,D020918,,,,
+BMGC_DS19527,BMG_DS075755,,Chronic Regional Pain Syndrome,Complex Regional Pain Syndromes,,,,,,C5828567,D020918,,,,
+BMGC_DS19528,BMG_DS075756,,Mitochondrial Defect,Mitochondrial Diseases,,,,,,C5828574,D028361,,,,
+BMGC_DS19529,BMG_DS075758,,Chronic Secondary Pain,Chronic Pain,,,,,,C5828595,D059350,,,,
+BMGC_DS19530,BMG_DS075765,,"SPERMATOGENIC FAILURE, X-LINKED, 5",,,,,DOID:0070596,X-linked spermatogenic failure 5,C5829558,,301099;312820,MONDO:0859477,"spermatogenic failure, X-linked, 5",
+BMGC_DS19531,BMG_DS075766,,"SPERMATOGENIC FAILURE, X-LINKED, 6",,,,,DOID:0070597,X-linked spermatogenic failure 6,C5829562,,300309;301101,MONDO:0859478,"spermatogenic failure, X-linked, 6",
+BMGC_DS19532,BMG_DS075767,,"SPERMATOGENIC FAILURE, X-LINKED, 7",,,,,DOID:0070598,X-linked spermatogenic failure 7,C5829567,,301106;301105,MONDO:0957202,"spermatogenic failure, X-linked, 7",
+BMGC_DS19533,BMG_DS075768,,,,,,,,,C5829568,,301107,MONDO:0957203,"intellectual developmental disorder, X-linked 111",
+BMGC_DS19534,BMG_DS075769,,"CATARACTS, HEARING IMPAIRMENT, NEPHROTIC SYNDROME, AND ENTEROCOLITIS 1",,,,,,,C5829571,,300126;301108,MONDO:0958178,"cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1",
+BMGC_DS19535,BMG_DS075770,,"AUTOINFLAMMATORY DISEASE, MULTISYSTEM, WITH IMMUNE DYSREGULATION, X-LINKED",,,,,,,C5829577,,300681;301109,MONDO:0957494,"autoinflammatory disease, multisystem, with immune dysregulation, X-linked",
+BMGC_DS19536,BMG_DS075771,,"HEMOLYTIC UREMIC SYNDROME, ATYPICAL, 8, WITH RHIZOMELIC SHORT STATURE",,,,,,,C5829585,,300611;301110,MONDO:0957495,"hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature",
+BMGC_DS19537,BMG_DS075772,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 112",,,,,,,C5829589,,301111;300061,MONDO:0957496,"intellectual developmental disorder, X-linked 112",
+BMGC_DS19538,BMG_DS075773,,,,,,,,,C5829874,,608415,MONDO:0958180,prolonged electroretinal response suppression 1,
+BMGC_DS19539,BMG_DS075774,,"CONGENITAL MYOPATHY 4B, AUTOSOMAL RECESSIVE",,,,,,,C5829889,,609284;191030,MONDO:0012239,"congenital myopathy 4B, autosomal recessive",
+BMGC_DS19540,BMG_DS075775,,CONE-ROD DYSTROPHY 23,,,,,,,C5829987,,613425;613428,,,
+BMGC_DS19541,BMG_DS075776,,"MACULAR DYSTROPHY, RETINAL, 5",,,,,DOID:0111021,cone-rod dystrophy 15,C5829994,,609502;613660,,,
+BMGC_DS19542,BMG_DS075777,,"CARDIOMYOPATHY, DILATED, 1PP",,,,,DOID:0110327,hypertrophic cardiomyopathy 26,C5830134,,617047,,,
+BMGC_DS19543,BMG_DS075778,,ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 15,,,,,DOID:0110327,hypertrophic cardiomyopathy 26,C5830135,,617047,,,
+BMGC_DS19544,BMG_DS075780,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, DYSMORPHIC FACIES, AND SKELETAL ANOMALIES, WITH OR WITHOUT SEIZURES",,,,,,,C5830244,,608961;620224,MONDO:0859365,"neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures",
+BMGC_DS19545,BMG_DS075781,,,,,,,,,C5830269,,620237,MONDO:0859373,"intellectual developmental disorder, autosomal recessive 78",
+BMGC_DS19546,BMG_DS075782,,"DEVELOPMENTAL DELAY WITH HYPOTONIA, MYOPATHY, AND BRAIN ABNORMALITIES",,,,,,,C5830270,,602580;620240,MONDO:0859375,"developmental delay with hypotonia, myopathy, and brain abnormalities",
+BMGC_DS19547,BMG_DS075783,,,,,,,,,C5830272,,620241,MONDO:0859376,"hydrocephalus, congenital, 5, susceptibility to",
+BMGC_DS19548,BMG_DS075784,,NEURODEVELOPMENTAL DISORDER WITH POOR GROWTH AND BEHAVIORAL ABNORMALITIES,,,,,DOID:0081444,neurodevelopmental disorder with poor growth and behavioral abnormalities,C5830273,,620242;609126,MONDO:0859377,neurodevelopmental disorder with poor growth and behavioral abnormalities,
+BMGC_DS19549,BMG_DS075785,,"LEUKODYSTROPHY, HYPOMYELINATING, 25",,,,,DOID:0070401,hypomyelinating leukodystrophy 25,C5830275,,618978;620243,MONDO:0859378,"leukodystrophy, hypomyelinating, 25",
+BMGC_DS19550,BMG_DS075786,,LYMPHATIC MALFORMATION 13,,,,,,,C5830279,,620244;616821,MONDO:0859379,lymphatic malformation 13,
+BMGC_DS19551,BMG_DS075787,,EPISODIC KINESIGENIC DYSKINESIA 3,,,,,DOID:0060944,episodic kinesigenic dyskinesia 3,C5830280,,620245;620108,MONDO:0859380,episodic kinesigenic dyskinesia 3,
+BMGC_DS19552,BMG_DS075788,,CONGENITAL MYOPATHY 18,,,,,DOID:0081350,congenital myopathy 18,C5830283,,620246,MONDO:0859514,congenital myopathy 18,
+BMGC_DS19553,BMG_DS075789,,"CARDIOMYOPATHY, DILATED, 1OO",,,,,,,C5830291,,620247,MONDO:0859381,"cardiomyopathy, dilated, 100",
+BMGC_DS19554,BMG_DS075790,,"NEURODEVELOPMENTAL DISORDER WITH SEIZURES, SPASTICITY, AND COMPLETE OR PARTIAL AGENESIS OF THE CORPUS CALLOSUM",,,,,,,C5830296,,620250,MONDO:0859516,"neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum",
+BMGC_DS19555,BMG_DS075791,,CATARACT 50 WITH OR WITHOUT GLAUCOMA,,,,,,,C5830299,,608961;620253,MONDO:0859382,cataract 50 with or without glaucoma,
+BMGC_DS19556,BMG_DS075792,,"CONGENITAL MYOPATHY 2B, SEVERE INFANTILE, AUTOSOMAL RECESSIVE",,,,,DOID:0081339,congenital myopathy 2B,C5830300,,102610;620265,MONDO:0859517,"congenital myopathy 2b, severe infantile, autosomal recessive",
+BMGC_DS19557,BMG_DS075793,,"LEUKODYSTROPHY, HYPOMYELINATING, 26, WITH CHONDRODYSPLASIA",,,,,DOID:0070403,hypomyelinating leukodystrophy 26,C5830312,,620269;610788,MONDO:0859518,"leukodystrophy, hypomyelinating, 26, with chondrodysplasia",
+BMGC_DS19558,BMG_DS075794,,,,,,,,,C5830319,,620270,MONDO:0859519,neurodevelopmental disorder with absent speech and movement and behavioral abnormalities,
+BMGC_DS19559,BMG_DS075795,,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 23",,,,,DOID:0070485,mitochondrial complex IV deficiency nuclear type 23,C5830322,,620275;603648,MONDO:0859520,"mitochondrial complex IV deficiency, nuclear type 23",
+BMGC_DS19560,BMG_DS075796,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 14,,,,,,,C5830326,,603618;620276,MONDO:0859521,oocyte maturation defect 14,
+BMGC_DS19561,BMG_DS075797,,SPERMATOGENIC FAILURE 81,,,,,DOID:0070580,spermatogenic failure 81,C5830329,,612683;620277,MONDO:0859522,spermatogenic failure 81,
+BMGC_DS19562,BMG_DS075798,,"CONGENITAL MYOPATHY 2C, SEVERE INFANTILE, AUTOSOMAL DOMINANT",,,,,DOID:0081340,congenital myopathy 2C,C5830333,,620278;102610,MONDO:0859523,"congenital myopathy 2c, severe infantile, autosomal dominant",
+BMGC_DS19563,BMG_DS075799,,"DEAFNESS, AUTOSOMAL DOMINANT 86",,,,,DOID:0070610,autosomal dominant nonsyndromic deafness 86,C5830340,,620280;606930,MONDO:0859524,"hearing loss, autosomal dominant 86",
+BMGC_DS19564,BMG_DS075800,,"DEAFNESS, AUTOSOMAL DOMINANT 87",,,,,DOID:0070606,autosomal dominant nonsyndromic deafness 87,C5830342,,602758;620281,MONDO:0859525,"hearing loss, autosomal dominant 87",
+BMGC_DS19565,BMG_DS075801,,IMMUNODEFICIENCY 109 WITH LYMPHOPROLIFERATION,,,,,,,C5830346,,602250;620282,MONDO:0859526,immunodeficiency 109 with lymphoproliferation,
+BMGC_DS19566,BMG_DS075802,,"DEAFNESS, AUTOSOMAL DOMINANT 88",,,,,DOID:0070611,autosomal dominant nonsyndromic deafness 88,C5830355,,611123;620283,MONDO:0859527,"hearing loss, autosomal dominant 88",
+BMGC_DS19567,BMG_DS075803,,"DEAFNESS, AUTOSOMAL DOMINANT 89",,,,,DOID:0070612,autosomal dominant nonsyndromic deafness 89,C5830357,,620284;601461,MONDO:0859528,"hearing loss, autosomal dominant 89",
+BMGC_DS19568,BMG_DS075804,,"AMYOTROPHIC LATERAL SCLEROSIS 27, JUVENILE",,,,,DOID:0081381,juvenile amyotrophic lateral sclerosis type 27,C5830359,,605712;620285,MONDO:0859529,"amyotrophic lateral sclerosis 27, juvenile",
+BMGC_DS19569,BMG_DS075805,,"MYOPATHY, SARCOPLASMIC BODY",,,,,,,C5830362,,160000;620286,MONDO:0859530,"myopathy, sarcoplasmic body",
+BMGC_DS19570,BMG_DS075806,,"NEURODEVELOPMENTAL DISORDER WITH LANGUAGE DELAY AND BEHAVIORAL ABNORMALITIES, WITH OR WITHOUT SEIZURES",,,,,,,C5830365,,620292;606228,MONDO:0859531,"neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures",
+BMGC_DS19571,BMG_DS075807,,,,,,,,,C5830367,,620294,MONDO:0859532,"congenital heart defects, multiple types, 9",
+BMGC_DS19572,BMG_DS075808,,AUTOINFLAMMATION WITH PULMONARY AND CUTANEOUS VASCULITIS,,,,,,,C5830371,,620296;142370,MONDO:0957204,autoinflammation with pulmonary and cutaneous vasculitis,
+BMGC_DS19573,BMG_DS075809,,MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY 2,,,,,DOID:0060999,mitochondrial trifunctional protein deficiency 2,C5830374,,143450;620300,MONDO:0958185,mitochondrial trifunctional protein deficiency 2,
+BMGC_DS19574,BMG_DS075810,,"PITUITARY HORMONE DEFICIENCY, COMBINED OR ISOLATED, 8",,,,,DOID:0061018,combined or isolated pituitary hormone deficiency 8,C5830375,,620303,MONDO:0957208,"pituitary hormone deficiency, combined or isolated, 8",
+BMGC_DS19575,BMG_DS075811,,NEUROOCULORENAL SYNDROME,,,,,,,C5830377,,602430;620305,MONDO:0957210,neurooculorenal syndrome,
+BMGC_DS19576,BMG_DS075812,,NEURODEGENERATION AND SEIZURES DUE TO COPPER TRANSPORT DEFECT,,,,,,,C5830385,,603085;620306,MONDO:0957211,neurodegeneration and seizures due to copper transport defect,
+BMGC_DS19577,BMG_DS075813,,CONGENITAL MYOPATHY 20,,,,,DOID:0081352,congenital myopathy 20,C5830393,,620310;180903,MONDO:0957215,congenital myopathy 20,
+BMGC_DS19578,BMG_DS075814,,PREMATURE OVARIAN FAILURE 21,,,,,,,C5830399,,603273;620311,MONDO:0957216,premature ovarian failure 21,
+BMGC_DS19579,BMG_DS075815,,LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER 2,,,,,DOID:0070373,leukoencephalopathy with vanishing white matter 2,C5830404,,606454;620312,MONDO:0957870,leukoencephalopathy with vanishing white matter 2,
+BMGC_DS19580,BMG_DS075816,,LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER 3,,,,,DOID:0070372,leukoencephalopathy with vanishing white matter 3,C5830405,,606273;620313,MONDO:0957871,leukoencephalopathy with vanishing white matter 3,
+BMGC_DS19581,BMG_DS075817,,LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER 4,,,,,DOID:0070371,leukoencephalopathy with vanishing white matter 4,C5830406,,620314;606687,MONDO:0957872,leukoencephalopathy with vanishing white matter 4,
+BMGC_DS19582,BMG_DS075818,,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 12",,,,,,,C5830407,,613774;620316,MONDO:0957217,"cortical dysplasia, complex, with other brain malformations 12",
+BMGC_DS19583,BMG_DS075819,,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND SPEECH DELAY, WITH OR WITHOUT BRAIN ABNORMALITIES",,,,,,,C5830413,,191050;620317,MONDO:0957218,"neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities",
+BMGC_DS19584,BMG_DS075820,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 17,,,,,,,C5830418,,614107;620319,MONDO:0957220,oocyte/zygote/embryo maturation arrest 17,
+BMGC_DS19585,BMG_DS075821,,"HEMATURIA, BENIGN FAMILIAL, 2",,,,,,,C5830421,,120070;620320,MONDO:0958186,"hematuria, benign familial, 2",
+BMGC_DS19586,BMG_DS075822,,C1q DEFICIENCY 2,,,,,,,C5830422,,620321,MONDO:0958187,C1Q deficiency 2,
+BMGC_DS19587,BMG_DS075823,,C1q DEFICIENCY 3,,,,,,,C5830423,,620322,MONDO:0958188,C1Q deficiency 3,
+BMGC_DS19588,BMG_DS075824,,CONGENITAL MYOPATHY 21 WITH EARLY RESPIRATORY FAILURE,,,,,DOID:0081353,congenital myopathy 21,C5830424,,620326;611327,MONDO:0957224,congenital myopathy 21 with early respiratory failure,
+BMGC_DS19589,BMG_DS075825,,"NEURODEGENERATION WITH DEVELOPMENTAL DELAY, EARLY RESPIRATORY FAILURE, MYOCLONIC SEIZURES, AND BRAIN ABNORMALITIES",,,,,,,C5830433,,612383;620327,MONDO:0957225,"neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities",
+BMGC_DS19590,BMG_DS075826,,,,,,,,,C5830437,,620330,MONDO:0957228,"intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities",
+BMGC_DS19591,BMG_DS075827,,HATIPOGLU IMMUNODEFICIENCY SYNDROME,,,,,,,C5830439,,608258;620331,MONDO:0957229,hatipoglu immunodeficiency syndrome,
+BMGC_DS19592,BMG_DS075828,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 18,,,,,,,C5830441,,609364;620332,MONDO:0957230,oocyte/zygote/embryo maturation arrest 18,
+BMGC_DS19593,BMG_DS075829,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 19,,,,,,,C5830442,,620333;609658,MONDO:0957231,oocyte/zygote/embryo maturation arrest 19,
+BMGC_DS19594,BMG_DS075830,,CONE-ROD DYSTROPHY 24,,,,,DOID:0081449,cone-rod dystrophy 24,C5830446,,604011;620342,MONDO:0957240,cone-rod dystrophy 24,
+BMGC_DS19595,BMG_DS075831,,,,,,,,,C5830451,,620343,MONDO:0958189,basal cell nevus syndrome 2,
+BMGC_DS19596,BMG_DS075832,,,,,,,,,C5830452,,620344,MONDO:0958190,prolonged electroretinal response suppression 2,
+BMGC_DS19597,BMG_DS075833,,"CONGENITAL MYOPATHY 22A, CLASSIC",,,,,DOID:0081354,congenital myopathy 22A,C5830453,,603967;620351,MONDO:0957247,"congenital myopathy 22A, classic",
+BMGC_DS19598,BMG_DS075834,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 31B,,,,,DOID:0070376,developmental and epileptic encephalopathy 31B,C5830459,,602377;620352,MONDO:0957248,"developmental and epileptic encephalopathy, 31B",
+BMGC_DS19599,BMG_DS075835,,SPERMATOGENIC FAILURE 82,,,,,DOID:0070581,spermatogenic failure 82,C5830468,,604689;620353,MONDO:0957249,spermatogenic failure 82,
+BMGC_DS19600,BMG_DS075836,,SPERMATOGENIC FAILURE 83,,,,,DOID:0070582,spermatogenic failure 83,C5830470,,602135;620354,MONDO:0957250,spermatogenic failure 83,
+BMGC_DS19601,BMG_DS075837,,"CILIARY DYSKINESIA, PRIMARY, 50",,,,,,,C5830473,,610061;620356,MONDO:0957252,"ciliary dyskinesia, primary, 50",
+BMGC_DS19602,BMG_DS075838,,DIARRHEA 13,,,,,,,C5830477,,620357;605677,MONDO:0957253,diarrhea 13,
+BMGC_DS19603,BMG_DS075839,,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4A",,,,,DOID:0070461,mitochondrial complex V (ATP synthase) deficiency nuclear type 4A,C5830480,,620358;164360,MONDO:0957254,"mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A",
+BMGC_DS19604,BMG_DS075840,,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 7",,,,,DOID:0070464,mitochondrial complex V (ATP synthase) deficiency nuclear type 7,C5830482,,600828;620359,MONDO:0957255,"mitochondrial complex V (ATP synthase) deficiency, nuclear type 7",
+BMGC_DS19605,BMG_DS075841,,,,,,,,,C5830484,,620364,MONDO:0957260,combined low LDL and fibrinogen,
+BMGC_DS19606,BMG_DS075842,,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 7",,,,,,,C5830485,,617868;620365,MONDO:0957261,"pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7",
+BMGC_DS19607,BMG_DS075843,,"OSTEOPETROSIS, AUTOSOMAL RECESSIVE 9",,,,,,,C5830487,,109280;620366,MONDO:0957262,"osteopetrosis, autosomal recessive 9",
+BMGC_DS19608,BMG_DS075844,,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 8",,,,,,,C5830496,,620367;606478,MONDO:0957263,"pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8",
+BMGC_DS19609,BMG_DS075845,,CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 3,,,,,,,C5830497,,606478;620368,MONDO:0957264,cerebroretinal microangiopathy with calcifications and cysts 3,
+BMGC_DS19610,BMG_DS075846,,"CONGENITAL MYOPATHY 22B, SEVERE FETAL",,,,,DOID:0081355,congenital myopathy 22B,C5830501,,603967;620369,MONDO:0957265,"congenital myopathy 22B, severe fetal",
+BMGC_DS19611,BMG_DS075847,,RECON PROGEROID SYNDROME,,,,,,,C5830504,,600537;620370,MONDO:0957266,RECON progeroid syndrome,
+BMGC_DS19612,BMG_DS075848,,"NEURODEVELOPMENTAL DISORDER WITH INTRACRANIAL HEMORRHAGE, SEIZURES, AND SPASTICITY",,,,,,,C5830509,,620371;614281,MONDO:0957267,"neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity",
+BMGC_DS19613,BMG_DS075849,,HYPERSULFATURIA,,,,,,,C5830511,,610130;620372,MONDO:0957268,hypersulfaturia,
+BMGC_DS19614,BMG_DS075850,,"NEPHROLITHIASIS, CALCIUM OXALATE, 2, WITH OR WITHOUT NEPHROCALCINOSIS",,,,,,,C5830516,,620374,MONDO:0958191,"nephrolithiasis, calcium oxalate, 2, with or without nephrocalcinosis",
+BMGC_DS19615,BMG_DS075851,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 28",,,,,,,C5830518,,142910;620375,MONDO:0957270,"muscular dystrophy, limb-girdle, autosomal recessive 28",
+BMGC_DS19616,BMG_DS075852,,"AUTOINFLAMMATORY DISEASE, SYSTEMIC, WITH VASCULITIS",,,,,,,C5830525,,165120;620376,MONDO:0957271,"autoinflammatory disease, systemic, with vasculitis",
+BMGC_DS19617,BMG_DS075853,,"SPASTIC PARAPLEGIA 89, AUTOSOMAL RECESSIVE",,,,,DOID:0070458,hereditary spastic paraplegia 89,C5830531,,620379;603243,MONDO:0957274,"spastic paraplegia 89, autosomal recessive",
+BMGC_DS19618,BMG_DS075854,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 20,,,,,,,C5830539,,190060;620383,MONDO:0957278,oocyte/zygote/embryo maturation arrest 20,
+BMGC_DS19619,BMG_DS075855,,"AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT 2",,,,,,,C5830542,,605868;620384,MONDO:0957279,"auditory neuropathy, autosomal dominant 2",
+BMGC_DS19620,BMG_DS075856,,"NEMALINE MYOPATHY 5B, AUTOSOMAL RECESSIVE, CHILDHOOD-ONSET",,,,,DOID:0081374,nemaline myopathy 5B,C5830545,,191041;620386,MONDO:0957281,"nemaline myopathy 5B, autosomal recessive, childhood-onset",
+BMGC_DS19621,BMG_DS075857,,"NEMALINE MYOPATHY 5C, AUTOSOMAL DOMINANT",,,,,DOID:0081375,nemaline myopathy 5C,C5830549,,620389;191041,MONDO:0957284,"nemaline myopathy 5C, autosomal dominant",
+BMGC_DS19622,BMG_DS075858,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 79",,,,,,,C5830553,,620393;189940,MONDO:0957288,"intellectual developmental disorder, autosomal recessive 79",
+BMGC_DS19623,BMG_DS075859,,GLYCINE ENCEPHALOPATHY 2,,,,,DOID:0061001,glycine encephalopathy 2,C5830559,,238310;620398,MONDO:0958192,glycine encephalopathy 2,
+BMGC_DS19624,BMG_DS075860,,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 9",,,,,,,C5830560,,606471;620400,MONDO:0957294,"pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9",
+BMGC_DS19625,BMG_DS075861,,SPERMATOGENIC FAILURE 84,,,,,DOID:0070583,spermatogenic failure 84,C5830562,,620381;620409,MONDO:0957301,spermatogenic failure 84,
+BMGC_DS19626,BMG_DS075862,,"SPASTIC PARAPLEGIA 90A, AUTOSOMAL DOMINANT",,,,,DOID:0070459,hereditary spastic paraplegia 90A,C5830574,,620416;613540,MONDO:0957308,"spastic paraplegia 90A, autosomal dominant",
+BMGC_DS19627,BMG_DS075863,,"SPASTIC PARAPLEGIA 90B, AUTOSOMAL RECESSIVE",,,,,DOID:0070460,hereditary spastic paraplegia 90B,C5830578,,613540;620417,MONDO:0957309,"spastic paraplegia 90B, autosomal recessive",
+BMGC_DS19628,BMG_DS075864,,RETINITIS PIGMENTOSA 97,,,,,,,C5830579,,617509;620422,MONDO:0957314,retinitis pigmentosa 97,
+BMGC_DS19629,BMG_DS075865,,MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 7,,,,,,,C5830586,,238330;620423,MONDO:0957382,multiple mitochondrial dysfunctions syndrome 7,
+BMGC_DS19630,BMG_DS075866,,"CATARACTS, HEARING IMPAIRMENT, NEPHROTIC SYNDROME, AND ENTEROCOLITIS 2",,,,,,,C5830590,,620425;606471,MONDO:0958193,"cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2",
+BMGC_DS19631,BMG_DS075867,,"DYSTONIA 37, EARLY-ONSET, WITH STRIATAL LESIONS",,,,,DOID:0060956,"dystonia 37, early-onset with striatal lesions",C5830592,,607607;620427,MONDO:0957385,"dystonia 37, early-onset, with striatal lesions",
+BMGC_DS19632,BMG_DS075868,,"NEURODEVELOPMENTAL DISORDER WITH MOTOR AND LANGUAGE DELAY, OCULAR DEFECTS, AND BRAIN ABNORMALITIES",,,,,DOID:0081387,"neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities",C5830596,,611354;620428,MONDO:0957386,"neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities",
+BMGC_DS19633,BMG_DS075869,,"AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 3",,,,,,,C5830600,,604491;620430,MONDO:0957388,"autoimmune disease, multisystem, infantile-onset, 3",
+BMGC_DS19634,BMG_DS075870,,"CILIARY DYSKINESIA, PRIMARY, 51",,,,,,,C5830608,,617824;620438,MONDO:0957396,"ciliary dyskinesia, primary, 51",
+BMGC_DS19635,BMG_DS075871,,,,,,,,,C5830612,,620439,MONDO:0957397,"intellectual developmental disorder, autosomal dominant 72",
+BMGC_DS19636,BMG_DS075872,,,,,,,,,C5830615,,620442,MONDO:0957530,"breast-ovarian cancer, familial, susceptibility to, 5",
+BMGC_DS19637,BMG_DS075873,,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND MOVEMENT ABNORMALITIES,,,,,,,C5830624,,614425;620445,MONDO:0957531,neurodevelopmental disorder with microcephaly and movement abnormalities,
+BMGC_DS19638,BMG_DS075874,,MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 3,,,,,,,C5830625,,605948;620447,MONDO:0957533,megalencephalic leukoencephalopathy with subcortical cysts 3,
+BMGC_DS19639,BMG_DS075875,,"MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 4, REMITTING",,,,,,,C5830628,,600308;620448,MONDO:0957534,"megalencephalic leukoencephalopathy with subcortical cysts 4, remitting",
+BMGC_DS19640,BMG_DS075876,,IMMUNODEFICIENCY 112,,,,,,,C5830633,,620449;604655,MONDO:0957535,immunodeficiency 112,
+BMGC_DS19641,BMG_DS075877,,,,,,,,,C5830636,,620450,MONDO:0957536,"intellectual developmental disorder, autosomal dominant 73",
+BMGC_DS19642,BMG_DS075878,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 58,,,,,,,C5830641,,620451;616422,MONDO:0957537,combined oxidative phosphorylation deficiency 58,
+BMGC_DS19643,BMG_DS075879,,AMYOTROPHIC LATERAL SCLEROSIS 28,,,,,DOID:0081382,amyotrophic lateral sclerosis type 28,C5830642,,618299;620452,MONDO:0957538,amyotrophic lateral sclerosis 28,
+BMGC_DS19644,BMG_DS075880,,"DYSTONIA 22, JUVENILE-ONSET",,,,,DOID:0060966,"dystonia 22, juvenile-onset",C5830645,,610764;620453,MONDO:0957539,"dystonia 22, juvenile-onset",
+BMGC_DS19645,BMG_DS075881,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIaa",,,,,,,C5830651,,620454,MONDO:0957540,"congenital disorder of glycosylation, type IIaa",
+BMGC_DS19646,BMG_DS075882,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND SPEECH DELAY, WITH OR WITHOUT SEIZURES",,,,,DOID:0070512,neurodevelopmental disorder with hypotonia and speech delay,C5830654,,620455,MONDO:0957541,"neurodevelopmental disorder with hypotonia and speech delay, with or without seizures",
+BMGC_DS19647,BMG_DS075883,,"DYSTONIA 22, ADULT-ONSET",,,,,DOID:0060967,"dystonia 22, adult-onset",C5830658,,620456;610764,MONDO:0957542,"dystonia 22, adult-onset",
+BMGC_DS19648,BMG_DS075884,,AURICULOCONDYLAR SYNDROME 4,,,,,,,C5830659,,606543;620457,MONDO:0957543,auriculocondylar syndrome 4,
+BMGC_DS19649,BMG_DS075885,,AURICULOCONDYLAR SYNDROME 2B,,,,,,,C5830664,,600810;620458,MONDO:0957544,auriculocondylar syndrome 2B,
+BMGC_DS19650,BMG_DS075886,,BIRT-HOGG-DUBE SYNDROME 2,,,,,,,C5830676,,618319;620459,MONDO:0800455,Birt-Hogg-Dube syndrome 2,
+BMGC_DS19651,BMG_DS075887,,OCULOPHARYNGEAL MUSCULAR DYSTROPHY 2,,,,,,,C5830682,,600124;620460,MONDO:0958195,oculopharyngeal muscular dystrophy 2,
+BMGC_DS19652,BMG_DS075888,,"CARDIOMYOPATHY, DILATED, 2I",,,,,,,C5830685,,620462;618385,MONDO:0957545,"cardiomyopathy, dilated, 2I",
+BMGC_DS19653,BMG_DS075890,,"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 15",,,,,DOID:0110327,hypertrophic cardiomyopathy 26,C5830688,,102565;617047,,,
+BMGC_DS19654,BMG_DS075894,,MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY 2 WITH MYOPATHY AND NEUROPATHY,,,,,DOID:0060999,mitochondrial trifunctional protein deficiency 2,C5830693,,143450;620300,,,
+BMGC_DS19655,BMG_DS075898,,,,,,,,,C5830701,,117000,MONDO:0007294,central core myopathy,
+BMGC_DS19656,BMG_DS075901,,MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY 1 WITH MYOPATHY AND NEUROPATHY,,,,,DOID:0070619,mitochondrial trifunctional protein deficiency 1,C5830705,,600890;609015,,,
+BMGC_DS19657,BMG_DS075960,718222000,Autosomal dominant popliteal pterygium syndrome,,,,,,,C5848052,,119500,MONDO:0007334,autosomal dominant popliteal pterygium syndrome,Autosomal dominant popliteal pterygium syndrome (disorder) | Autosomal dominant popliteal pterygium syndrome | Facio-genito-popliteal syndrome | Popliteal web syndrome
+BMGC_DS19658,BMG_DS075964,,"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA",,,,,,,C5848058,,219100;604580,MONDO:0009052,"cutis laxa, autosomal recessive, type 1A",
+BMGC_DS19659,BMG_DS075985,124275001,Deficiency of hypoxanthine phosphoribosyltransferase,,,,,,,C5848153,,,MONDO:0016088,hypoxanthine-guanine phosphoribosyltransferase deficiency,Deficiency of hypoxanthine-guanine phosphoribosyltransferase | Deficiency of guanine phosphoribosyltransferase | Deficiency of IMP pyrophosphorylase | Deficiency of hypoxanthine phosphoribosyltransferase | Deficiency of hypoxanthine phosphoribosyltransferase (disorder)
+BMGC_DS19660,BMG_DS075988,421527008,Resistance to activated protein C due to factor V Leiden mutation,,,,,,,C5848173,,,,,Activated protein C resistance | Resistance to activated protein C due to factor V Leiden mutation | Resistance to activated protein C due to factor V Leiden mutation (disorder) | Resistance to activated protein C caused by factor V R506Q mutation
+BMGC_DS19661,BMG_DS075991,,MYOCLONIC EPILEPSY OF LAFORA 1,,,,,,,C5848203,,254780;607566,MONDO:0958199,myoclonic epilepsy of Lafora 1,
+BMGC_DS19662,BMG_DS075996,205550003,Lamellar ichthyosis (disorder),,,,,,,C5848247,,,MONDO:0017778,lamellar ichthyosis,Lamellar ichthyosis | Collodion baby | Lamellar ichthyosis (disorder)
+BMGC_DS19663,BMG_DS075998,154835002,Secondary polycythemia,,3A81.Z,"Acquired polycythaemia, unspecified",D75.1,DOID:0060474,familial erythrocytosis 2,C5848252,,,,,Secondary polycythaemia | Secondary polycythemia | Secondary polycythaemia (disorder)
+BMGC_DS19664,BMG_DS075999,1336117005,Hemophilia B Leyden,Hemophilia B,,,,,,C5848256,D002836,,MONDO:0850054,hemophilia B leyden,Hemophilia B Leyden (disorder) | Haemophilia B Leyden | Factor 9 deficiency Leyden type | Factor IX deficiency Leyden type | Hemophilia B Leyden
+BMGC_DS19665,BMG_DS076000,373662000,Primary adrenocortical insufficiency,,5A74.0,Acquired adrenocortical insufficiency,E27.1,,,C5848257,,,,,Primary adrenocortical insufficiency (disorder) | Primary adrenocortical insufficiency | Primary hypoadrenalism
+BMGC_DS19666,BMG_DS076002,,"Spinal Muscular Atrophy, Infantile",Spinal Muscular Atrophies of Childhood,,,,,,C5848259,D014897,253300,MONDO:0009669,"spinal muscular atrophy, type 1",
+BMGC_DS19667,BMG_DS076004,,Hearing Disorders,Hearing Disorders,,,,,,C5848261,D006311,,,,
+BMGC_DS19668,BMG_DS076011,418470004;154768004;274090006,Porphyria (disorder),,,,,,,C5848305,,,MONDO:0037939,porphyria,Porphyria (disorder) | Porphyria | Porphyria | Porphyria (disorder)
+BMGC_DS19669,BMG_DS076012,,Porphyrias,Porphyrias,,,,,,C5848306,D011164,,,,
+BMGC_DS19670,BMG_DS076015,,DYSTONIA-DEAFNESS SYNDROME 1,,,,,,,C5848323,,102630;607371,MONDO:0011823,developmental malformations-deafness-dystonia syndrome,
+BMGC_DS19671,BMG_DS076020,715789009,Myotonia permanens,,,,G71.19,,,C5848361,C538353,,MONDO:0020482,myotonia permanens,Myotonia permanens (disorder) | Myotonia permanens
+BMGC_DS19672,BMG_DS076029,,"IMMUNE DYSREGULATION, AUTOIMMUNITY, AND AUTOINFLAMMATION",,,,,,,C5848750,,172420;620514,MONDO:0957790,"immune dysregulation, autoimmunity, and autoinflammation",
+BMGC_DS19673,BMG_DS076030,,"BECKER NEVUS, ISOLATED",,,,,,,C5848751,,604919,,,
+BMGC_DS19674,BMG_DS076031,,"HYPER-IgE SYNDROME 6, AUTOSOMAL DOMINANT, WITH RECURRENT INFECTIONS",,,,,,,C5848786,,620532;601512,MONDO:0957807,"hyper-IgE syndrome 6, autosomal dominant, with recurrent infections",
+BMGC_DS19675,BMG_DS076075,,,,,,,DOID:0070624,B-lymphoblastic leukemia with MYC rearrangement,C5855476,,,,,
+BMGC_DS19676,BMG_DS076077,,,,,,,DOID:0070623,B-lymphoblastic leukemia with MEF2D rearrangement,C5855479,,,,,
+BMGC_DS19677,BMG_DS076078,,,,,,,DOID:0070628,B-lymphoblastic leukemia with ZNF384 rearrangement,C5855480,,,,,
+BMGC_DS19678,BMG_DS076079,,,,,,,DOID:0070625,B-lymphoblastic leukemia with NUTM1 rearrangement,C5855485,,,,,
+BMGC_DS19679,BMG_DS076081,,,,,,,DOID:0070626,B-lymphoblastic leukemia with PAX5alt,C5855502,,,,,
+BMGC_DS19680,BMG_DS076082,,,,,,,DOID:0070631,acute myeloid leukemia with FUS-ERG fusion,C5856227,,,,,
+BMGC_DS19681,BMG_DS076083,,,,,,,DOID:0070633,acute myeloid leukemia with NPM1-MLF1 fusion,C5856228,,,,,
+BMGC_DS19682,BMG_DS076084,,,,,,,DOID:0070627,B-lymphoblastic leukemia with TCF3-HLF fusion,C5856321,,,,,
+BMGC_DS19683,BMG_DS076421,,"ALPORT SYNDROME 3A, AUTOSOMAL DOMINANT",,,,,DOID:0110032,autosomal dominant Alport syndrome,C5882663,,104200;120070,MONDO:0007086,autosomal dominant Alport syndrome,
+BMGC_DS19684,BMG_DS076422,,LUI-JEE-BARON SYNDROME,,,,,,,C5882664,,301113;301114,MONDO:0957919,Lui-Jee-Baron syndrome,
+BMGC_DS19685,BMG_DS076423,,IMMUNODEFICIENCY 118,,,,,,,C5882665,,300587;301115,MONDO:0958030,immunodeficiency 118,
+BMGC_DS19686,BMG_DS076424,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 113",,,,,,,C5882666,,301116;300907,MONDO:0958200,"intellectual developmental disorder, x-linked 113",
+BMGC_DS19687,BMG_DS076425,,"AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL, 1",,,,,DOID:0061005,congenital amegakaryocytic thrombocytopenia 1,C5882667,,159530;604498,MONDO:0800452,congenital amegakaryocytic thrombocytopenia 1,
+BMGC_DS19688,BMG_DS076426,,TUMOR PREDISPOSITION SYNDROME 4,,,,,,,C5882668,,604373;609265,,,
+BMGC_DS19689,BMG_DS076427,,"SPASTIC PARAPLEGIA 72A, AUTOSOMAL DOMINANT",,,,,,,C5882669,,609347;615625,MONDO:0014282,hereditary spastic paraplegia 72,
+BMGC_DS19690,BMG_DS076428,,"EPILEPSY, EARLY-ONSET, 2, WITH OR WITHOUT DEVELOPMENTAL DELAY",,,,,DOID:0070471,early-onset epilepsy 2,C5882670,,618832,MONDO:0030005,"epilepsy, early-onset, with or without developmental delay",
+BMGC_DS19691,BMG_DS076429,,"EPIDERMOLYTIC HYPERKERATOSIS 2A, AUTOSOMAL DOMINANT",,,,,DOID:0081359,epidermolytic hyperkeratosis 2,C5882671,,620150;148080,MONDO:0700248,"epidermolytic hyperkeratosis 2A, autosomal dominant",
+BMGC_DS19692,BMG_DS076430,,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL RECESSIVE 9",,,,,DOID:0081428,autosomal recessive distal hereditary motor neuronopathy 9,C5882672,,601683;620402,MONDO:0957874,"neuronopathy, distal hereditary motor, autosomal recessive 9",
+BMGC_DS19693,BMG_DS076431,,,,,,,,,C5882673,,620461,MONDO:0957561,"encephalitis, acute, infection-induced, susceptibility to, 12",
+BMGC_DS19694,BMG_DS076432,,"EPILEPSY, EARLY-ONSET, 3, WITH OR WITHOUT DEVELOPMENTAL DELAY",,,,,DOID:0070472,early-onset epilepsy 3,C5882674,,620465,MONDO:0958196,"epilepsy, early-onset, 3, with or without developmental delay",
+BMGC_DS19695,BMG_DS076433,,"CRANIAL DYSINNERVATION DISORDER, CONGENITAL, WITH ABSENT CORNEAL REFLEX AND DEVELOPMENTAL DELAY",,,,,,,C5882675,,601726;620469,MONDO:0957563,"cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay",
+BMGC_DS19696,BMG_DS076434,,,,,,,,,C5882676,,620470,MONDO:0957564,"congenital smooth muscle hamartoma, with or without hemihypertrophy",
+BMGC_DS19697,BMG_DS076435,,"THROMBOCYTOPENIA 8, WITH DYSMORPHIC FEATURES AND DEVELOPMENTAL DELAY",,,,,,,C5882677,,102630;620475,,,
+BMGC_DS19698,BMG_DS076436,,THROMBOCYTOPENIA 9,,,,,,,C5882678,,620478;600044,MONDO:0957572,thrombocytopenia 9,
+BMGC_DS19699,BMG_DS076437,,"AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL, 2",,,,,DOID:0061002,congenital amegakaryocytic thrombocytopenia 2,C5882679,,620481;600044,MONDO:0957575,"amegakaryocytic thrombocytopenia, congenital, 2",
+BMGC_DS19700,BMG_DS076438,,"PARKINSON DISEASE 25, AUTOSOMAL RECESSIVE EARLY-ONSET, WITH IMPAIRED INTELLECTUAL DEVELOPMENT",,,,,DOID:0070486,Parkinson's disease 25,C5882680,,600756;620482,MONDO:0957576,"parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development",
+BMGC_DS19701,BMG_DS076439,,"VARIEGATE PORPHYRIA, CHILDHOOD-ONSET",,,,,,,C5882681,,600923;620483,MONDO:0957577,"variegate porphyria, childhood-onset",
+BMGC_DS19702,BMG_DS076440,,THROMBOCYTOPENIA 10,,,,,,,C5882682,,600925;620484,MONDO:0957578,thrombocytopenia 10,
+BMGC_DS19703,BMG_DS076441,,"BLEEDING DISORDER, PLATELET-TYPE, 25",,,,,,,C5882683,,620486;600317,MONDO:0957580,"bleeding disorder, platelet-type, 25",
+BMGC_DS19704,BMG_DS076442,,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES,,,,,DOID:0070513,neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities,C5882684,,600812;620489,MONDO:0957583,neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities,
+BMGC_DS19705,BMG_DS076443,,SPERMATOGENIC FAILURE 85,,,,,DOID:0070584,spermatogenic failure 85,C5882685,,612739;620490,MONDO:0957584,spermatogenic failure 85,
+BMGC_DS19706,BMG_DS076444,,"NEURODEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE, BEHAVIORAL ABNORMALITIES, AND DYSMORPHIC FACIES",,,,,,,C5882686,,620494;616472,MONDO:0957588,"neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies",
+BMGC_DS19707,BMG_DS076445,,SPERMATOGENIC FAILURE 87,,,,,DOID:0070586,spermatogenic failure 87,C5882687,,620500;102480,MONDO:0957594,spermatogenic failure 87,
+BMGC_DS19708,BMG_DS076446,,ZIEGLER-HUANG SYNDROME,,,,,,,C5882688,,611149;620501,MONDO:0957595,Ziegler-Huang syndrome,
+BMGC_DS19709,BMG_DS076447,,NEURODEVELOPMENTAL DISORDER WITH LANGUAGE DELAY AND VARIABLE COGNITIVE ABNORMALITIES,,,,,,,C5882689,,603540;620502,MONDO:0957779,neurodevelopmental disorder with language delay and variable cognitive abnormalities,
+BMGC_DS19710,BMG_DS076448,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 111,,,,,,,C5882690,,614191;620504,MONDO:0957780,developmental and epileptic encephalopathy 111,
+BMGC_DS19711,BMG_DS076449,,ICHTHYOSIS WITH ERYTHROKERATODERMA,,,,,,,C5882691,,620507;604434,MONDO:0957783,ichthyosis with erythrokeratoderma,
+BMGC_DS19712,BMG_DS076450,,XEROSIS AND GROWTH FAILURE WITH IMMUNE AND PULMONARY DYSFUNCTION SYNDROME,,,,,,,C5882692,,620510,MONDO:0957786,xerosis and growth failure with immune and pulmonary dysfunction syndrome,
+BMGC_DS19713,BMG_DS076451,,FLIEDNER-ZWEIER SYNDROME,,,,,,,C5882693,,616023;620511,MONDO:0957787,Fliedner-Zweier syndrome,
+BMGC_DS19714,BMG_DS076452,,"SPASTIC PARAPLEGIA 18A, AUTOSOMAL DOMINANT",,,,,,,C5882694,,611605;620512,MONDO:0957788,"spastic paraplegia 18a, autosomal dominant",
+BMGC_DS19715,BMG_DS076453,,"NEURODEVELOPMENTAL DISORDER WITH MOTOR REGRESSION, PROGRESSIVE SPASTIC PARAPLEGIA, AND OROMOTOR DYSFUNCTION",,,,,,,C5882695,,602777;620515,MONDO:0957791,"neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction",
+BMGC_DS19716,BMG_DS076454,,ARRHYTHMOGENIC CARDIOMYOPATHY WITH VARIABLE ECTODERMAL ABNORMALITIES,,,,,,,C5882696,,620519;607463,MONDO:0957795,arrhythmogenic cardiomyopathy with variable ectodermal abnormalities,
+BMGC_DS19717,BMG_DS076455,,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 11",,,,,DOID:0081400,autosomal dominant distal hereditary motor neuronopathy 11,C5882697,,620528;182810,MONDO:0957875,"neuronopathy, distal hereditary motor, autosomal dominant 11",
+BMGC_DS19718,BMG_DS076456,,"DEVELOPMENTAL DELAY, DYSMORPHIC FACIES, AND BRAIN ANOMALIES",,,,,DOID:0060933,"developmental delay, dysmorphic facies, and brain anomalies",C5882698,,191318;620535,MONDO:0957810,"developmental delay, dysmorphic facies, and brain anomalies",
+BMGC_DS19719,BMG_DS076457,,"ALPORT SYNDROME 3B, AUTOSOMAL RECESSIVE",,,,,,,C5882699,,120070;620536,MONDO:0957811,"Alport syndrome 3b, autosomal recessive",
+BMGC_DS19720,BMG_DS076458,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 112,,,,,,,C5882700,,620537,MONDO:0957812,developmental and epileptic encephalopathy 112,
+BMGC_DS19721,BMG_DS076459,,"SPASTIC PARAPLEGIA 91, AUTOSOMAL DOMINANT, WITH OR WITHOUT CEREBELLAR ATAXIA",,,,,,,C5882701,,182810;620538,MONDO:0957813,"spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia",
+BMGC_DS19722,BMG_DS076460,,DEVELOPMENTAL DELAY WITH OR WITHOUT EPILEPSY,,,,,,,C5882702,,620540,MONDO:0957815,developmental delay with or without epilepsy,
+BMGC_DS19723,BMG_DS076461,,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL RECESSIVE 10",,,,,DOID:0081429,autosomal recessive distal hereditary motor neuronopathy 10,C5882703,,620542;602168,MONDO:0957876,"neuronopathy, distal hereditary motor, autosomal recessive 10",
+BMGC_DS19724,BMG_DS076462,,"ARTHROGRYPOSIS, DISTAL, TYPE 12",,,,,,,C5882704,,607509;620545,MONDO:0957819,"arthrogryposis, distal, type 12",
+BMGC_DS19725,BMG_DS076463,,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIbb",,,,,,,C5882705,,606975;620546,MONDO:0957820,"congenital disorder of glycosylation, type IIbb",
+BMGC_DS19726,BMG_DS076464,,SPERMATOGENIC FAILURE 88,,,,,DOID:0070587,spermatogenic failure 88,C5882706,,618125;620547,MONDO:0957821,spermatogenic failure 88,
+BMGC_DS19727,BMG_DS076465,,PREMATURE OVARIAN FAILURE 22,,,,,,,C5882707,,620548;618125,MONDO:0957822,premature ovarian failure 22,
+BMGC_DS19728,BMG_DS076466,,OPTIC ATROPHY 14,,,,,,,C5882708,,620550;615497,MONDO:0957824,optic atrophy 14,
+BMGC_DS19729,BMG_DS076467,,"DEAFNESS, AUTOSOMAL RECESSIVE 121",,,,,,,C5882709,,610464;620551,MONDO:0957825,"hearing loss, autosomal recessive 121",
+BMGC_DS19730,BMG_DS076468,,CRANIOMETADIAPHYSEAL OSTEOSCLEROSIS WITH HIP DYSPLASIA,,,,,,,C5882710,,603816;620558,MONDO:0957832,craniometadiaphyseal osteosclerosis with hip dysplasia,
+BMGC_DS19731,BMG_DS076469,,IMMUNODEFICIENCY 113 WITH AUTOIMMUNITY AND AUTOINFLAMMATION,,,,,,,C5882711,,604227;620565,MONDO:0957920,immunodeficiency 113 with autoimmunity and autoinflammation,
+BMGC_DS19732,BMG_DS076470,,CORNELIA DE LANGE SYNDROME 6,,,,,DOID:0060970,Cornelia de Lange syndrome 6,C5882712,,608749;620568,MONDO:0957921,Cornelia de Lange syndrome 6,
+BMGC_DS19733,BMG_DS076471,,"LEBER-LIKE HEREDITARY OPTIC NEUROPATHY, AUTOSOMAL RECESSIVE 2",,,,,,,C5882713,,602985;620569,MONDO:0958197,"Leber-like hereditary optic neuropathy, autosomal recessive 2",
+BMGC_DS19734,BMG_DS076472,,"CILIARY DYSKINESIA, PRIMARY, 52",,,,,,,C5882714,,620570,MONDO:0957922,"ciliary dyskinesia, primary, 52",
+BMGC_DS19735,BMG_DS076473,,OTOSCLEROSIS 11,,,,,DOID:0060928,otosclerosis 11,C5882715,,603252;620576,MONDO:0957928,otosclerosis 11,
+BMGC_DS19736,BMG_DS076474,,OPTIC ATROPHY 15,,,,,,,C5882716,,614479;620583,MONDO:0957935,optic atrophy 15,
+BMGC_DS19737,BMG_DS076475,,GARG-MISHRA PROGEROID SYNDROME,,,,,,,C5882717,,620601;607980,MONDO:0957953,Garg-Mishra progeroid syndrome,
+BMGC_DS19738,BMG_DS076476,,,,,,,,,C5882718,,620602,MONDO:0957954,lymphatic malformation 14,
+BMGC_DS19739,BMG_DS076477,,"IMMUNODEFICIENCY 114, FOLATE-RESPONSIVE",,,,,,,C5882719,,620603;600424,MONDO:0957955,"immunodeficiency 114, folate-responsive",
+BMGC_DS19740,BMG_DS076478,,"SPASTIC PARAPLEGIA 72B, AUTOSOMAL RECESSIVE",,,,,,,C5882720,,609347;620606,MONDO:0957958,"spastic paraplegia 72b, autosomal recessive",
+BMGC_DS19741,BMG_DS076479,,LONG-OLSEN-DISTELMAIER SYNDROME,,,,,,,C5882721,,608267;620609,MONDO:0957960,Long-Olsen-Distelmaier syndrome,
+BMGC_DS19742,BMG_DS076480,,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 21,,,,,,,C5882722,,603078;620610,MONDO:0957961,oocyte/zygote/embryo maturation arrest 21,
+BMGC_DS19743,BMG_DS076481,,OPTIC ATROPHY 16,,,,,,,C5882723,,608205;620629,MONDO:0957978,optic atrophy 16,
+BMGC_DS19744,BMG_DS076482,,IMMUNODEFICIENCY 115 WITH AUTOINFLAMMATION,,,,,,,C5882724,,620632;612487,MONDO:0957981,immunodeficiency 115 with autoinflammation,
+BMGC_DS19745,BMG_DS076483,,"CARDIOMYOPATHY, DILATED, 2J",,,,,,,C5882725,,600362;620635,MONDO:0957984,"cardiomyopathy, dilated, 2j",
+BMGC_DS19746,BMG_DS076484,,"NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATAXIA AND COGNITIVE DECLINE",,,,,,,C5882726,,601178;620636,MONDO:0957985,"neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline",
+BMGC_DS19747,BMG_DS076485,,TAN-ALMURSHEDI SYNDROME,,,,,,,C5882727,,603952;620641,MONDO:0957990,Tan-Almurshedi syndrome,
+BMGC_DS19748,BMG_DS076486,,"CILIARY DYSKINESIA, PRIMARY, 53",,,,,,,C5882728,,620642;619564,MONDO:0957991,"ciliary dyskinesia, primary, 53",
+BMGC_DS19749,BMG_DS076487,,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 59,,,,,,,C5882730,,620646;611845,MONDO:0957992,combined oxidative phosphorylation deficiency 59,
+BMGC_DS19750,BMG_DS076488,,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 6",,,,,,,C5882731,,620647,MONDO:0957993,"progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6",
+BMGC_DS19751,BMG_DS076489,,"DIABETES, DEAFNESS, DEVELOPMENTAL DELAY, AND SHORT STATURE SYNDROME",,,,,,,C5882732,,601916;620651,MONDO:0957997,"diabetes, deafness, developmental delay, and short stature syndrome",
+BMGC_DS19752,BMG_DS076490,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 80, WITH VARIANT LISSENCEPHALY",,,,,,,C5882733,,600639;620653,MONDO:0957999,"intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly",
+BMGC_DS19753,BMG_DS076491,,THROMBOCYTOPENIA 11 WITH MULTIPLE CONGENITAL ANOMALIES AND DYSMORPHIC FACIES,,,,,,,C5882734,,179530;620654,MONDO:0958000,thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies,
+BMGC_DS19754,BMG_DS076492,,ALFADHEL SYNDROME,,,,,,,C5882735,,179502;620655,MONDO:0958001,Alfadhel syndrome,
+BMGC_DS19755,BMG_DS076493,,HOXHA-ALIU SYNDROME,,,,,,,C5882736,,620662;608739,MONDO:0958005,Hoxha-Aliu syndrome,
+BMGC_DS19756,BMG_DS076494,,"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GUO-CAMPEAU TYPE",,,,,,,C5882737,,608739;620663,MONDO:0958006,"spondyloepimetaphyseal dysplasia, Guo-Campeau type",
+BMGC_DS19757,BMG_DS076495,,"SPASTIC ATAXIA 10, AUTOSOMAL RECESSIVE",,,,,,,C5882738,,612898;620666,MONDO:0958009,"spastic ataxia 10, autosomal recessive",
+BMGC_DS19758,BMG_DS076496,,IMMUNODEFICIENCY 117,,,,,,,C5882739,,147575;620668,MONDO:0958011,immunodeficiency 117,
+BMGC_DS19759,BMG_DS076497,,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 9,,,,,,,C5882740,,134770;620669,MONDO:0958012,neurodegeneration with brain iron accumulation 9,
+BMGC_DS19760,BMG_DS076498,,"IMMUNODEFICIENCY, COMMON VARIABLE, 15",,,,,,,C5882741,,620670;609213,MONDO:0958013,"immunodeficiency, common variable, 15",
+BMGC_DS19761,BMG_DS076499,,"NEUTROPENIA, SEVERE CONGENITAL, 11, AUTOSOMAL DOMINANT",,,,,,,C5882742,,609213;620674,MONDO:0958017,"neutropenia, severe congenital, 11, autosomal dominant",
+BMGC_DS19762,BMG_DS076500,,"LEUKODYSTROPHY, HYPOMYELINATING, 27",,,,,,,C5882743,,616404;620675,MONDO:0958018,"leukodystrophy, hypomyelinating, 27",
+BMGC_DS19763,BMG_DS076501,,"LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 8",,,,,,,C5882744,,104210;620679,MONDO:0958022,"lipodystrophy, familial partial, type 8",
+BMGC_DS19764,BMG_DS076502,,"LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 5",,,,,,,C5882745,,123695;620680,MONDO:0958023,"lipodystrophy, congenital generalized, type 5",
+BMGC_DS19765,BMG_DS076503,,"LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 9",,,,,,,C5882746,,620683;613867,MONDO:0958034,"lipodystrophy, familial partial, type 9",
+BMGC_DS19766,BMG_DS076504,,PREMATURE OVARIAN FAILURE 23,,,,,,,C5882747,,617670;620686,MONDO:0958035,premature ovarian failure 23,
+BMGC_DS19767,BMG_DS076505,,MOYAMOYA DISEASE 7,,,,,,,C5882748,,610108;620687,MONDO:0958202,moyamoya disease 7,
+BMGC_DS19768,BMG_DS076506,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 74",,,,,,,C5882749,,164020;620688,MONDO:0958203,"intellectual developmental disorder, autosomal dominant 74",
+BMGC_DS19769,BMG_DS076507,,DEVELOPMENTAL DYSPLASIA OF THE HIP 3,,,,,,,C5882750,,107770;620690,MONDO:0958037,developmental dysplasia of the hip 3,
+BMGC_DS19770,BMG_DS076508,,YUKSEL-VOGEL-BAUER SYNDROME,,,,,,,C5882751,,620703;604090,MONDO:0958205,Yuksel-Vogel-Bauer syndrome,
+BMGC_DS19771,BMG_DS076509,,SPERMATOGENIC FAILURE 89,,,,,DOID:0070588,spermatogenic failure 89,C5882752,,615358;620705,MONDO:0958206,spermatogenic failure 89,
+BMGC_DS19772,BMG_DS076510,,"EPIDERMOLYTIC HYPERKERATOSIS 2B, AUTOSOMAL RECESSIVE",,,,,,,C5882753,,148080;620707,MONDO:0700245,"epidermolytic hyperkeratosis 2B, autosomal recessive",
+BMGC_DS19773,BMG_DS076511,,POLYDACTYLY-MACROCEPHALY SYNDROME,,,,,,,C5882754,,154950;620712,MONDO:0958227,polydactyly-macrocephaly syndrome,
+BMGC_DS19774,BMG_DS076512,,SPERMATOGENIC FAILURE 86,,,,,DOID:0070585,spermatogenic failure 86,C5882755,,604303;620499,MONDO:0957593,spermatogenic failure 86,
+BMGC_DS19775,BMG_DS076513,,"NEUTROPENIA, SEVERE CONGENITAL, 10, AUTOSOMAL RECESSIVE",,,,,,,C5882756,,604858;620534,MONDO:0957809,"neutropenia, severe congenital, 10, autosomal recessive",
+BMGC_DS19776,BMG_DS076514,,"OSTEOGENESIS IMPERFECTA, TYPE XXIII",,,,,,,C5882757,,612834;620639,MONDO:0957988,"osteogenesis imperfecta, type 23",
+BMGC_DS19777,BMG_DS076515,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 81",,,,,,,C5882758,,614217;620700,MONDO:0958204,"intellectual developmental disorder, autosomal recessive 81",
+BMGC_DS19778,BMG_DS076542,,"AMELOGENESIS IMPERFECTA, TYPE IIIA",,,,,,,C5886770,,130900;611927,MONDO:0007538,"amelogenesis imperfecta, type 3A",
+BMGC_DS19779,BMG_DS076544,,"Porphyria, Erythropoietic, Congenital","Porphyria, Erythropoietic",,,,,,C5886774,D017092,263700,MONDO:0009902,cutaneous porphyria,
+BMGC_DS19780,BMG_DS076545,,MICROPHTHALMIA/COLOBOMA 12,,,,,,,C5886785,,120200;607108,MONDO:0007350,"coloboma, ocular, autosomal dominant",
+BMGC_DS19781,BMG_DS076555,,Listeria monocytogenes Infections,Listeriosis,,,,,,C5886852,D008088,,,,
+BMGC_DS19782,BMG_DS076568,,"HYPERTRICHOSIS, CONGENITAL GENERALIZED, 2",,,,,,,C5887323,,307150,MONDO:0010614,X-linked congenital generalized hypertrichosis,
+BMGC_DS19783,BMG_DS076569,,"GROWTH HORMONE DEFICIENCY, ISOLATED PARTIAL",,,,,,,C5887324,,615925;601898,MONDO:0014403,short stature due to GHSR deficiency,
+BMGC_DS19784,BMG_DS076573,,SPINOCEREBELLAR ATAXIA 47,,,,,DOID:0111743,cerebellar ataxia type 47,C5888376,,607204;617931,,,
+BMGC_DS19785,BMG_DS076574,,AURONEURODENTAL SYNDROME,,,,,,,C5889721,,607073;620830,MONDO:0970998,auroneurodental syndrome,
+BMGC_DS19786,BMG_DS076576,,,,,,,,,C5889860,,620730,MONDO:0958238,"hyperemesis gravidarum, susceptibility to",
+BMGC_DS19787,BMG_DS076577,,"Albinism, Partial",Piebaldism,,,,,,C5890906,D016116,,,,
+BMGC_DS19788,BMG_DS076578,,Blastomyces dermatitidis Infection,Blastomycosis,,,,,,C5890966,D001759,,,,
+BMGC_DS19789,BMG_DS077374,,"ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1A/1B, DIGENIC",,,,,DOID:0060946;DOID:0060942,Ullrich congenital muscular dystrophy 1A | Ullrich congenital muscular dystrophy 1B,C5935566,,254090;620727,,,
+BMGC_DS19790,BMG_DS077375,,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 37",,,,,,,C5935567,,314980;301118,MONDO:0958322,"intellectual developmental disorder, x-linked, syndromic 37",
+BMGC_DS19791,BMG_DS077376,,"SPERMATOGENIC FAILURE, X-LINKED, 8",,,,,DOID:0070599,X-linked spermatogenic failure 8,C5935568,,301119,MONDO:0970943,"spermatogenic failure, x-linked, 8",
+BMGC_DS19792,BMG_DS077377,,,,,,,,,C5935569,,301120,MONDO:0971170,"prostate cancer, hereditary, X-linked 3",
+BMGC_DS19793,BMG_DS077378,,"SPASTIC PARAPLEGIA 30B, AUTOSOMAL RECESSIVE",,,,,,,C5935571,,601255;620607,MONDO:0971149,"spastic paraplegia 30b, autosomal recessive",
+BMGC_DS19794,BMG_DS077379,,"AMYLOIDOSIS, HEREDITARY SYSTEMIC 5",,,,,,,C5935572,,153450;620658,MONDO:0971009,"amyloidosis, hereditary systemic 5",
+BMGC_DS19795,BMG_DS077380,,"AMYLOIDOSIS, HEREDITARY SYSTEMIC 6",,,,,,,C5935573,,109700;620659,MONDO:0971010,"amyloidosis, hereditary systemic 6",
+BMGC_DS19796,BMG_DS077381,,"ENCEPHALOPATHY, PORPHYRIA-RELATED",,,,,,,C5935574,,609806;620704,MONDO:0958224,"encephalopathy, porphyria-related",
+BMGC_DS19797,BMG_DS077382,,"LEUKOENCEPHALOPATHY, PORPHYRIA-RELATED",,,,,,,C5935575,,609806;620711,MONDO:0958226,"leukoencephalopathy, porphyria-related",
+BMGC_DS19798,BMG_DS077383,,"DEAFNESS, AUTOSOMAL RECESSIVE 122",,,,,,,C5935576,,618203;620714,MONDO:0958228,"hearing loss, autosomal recessive 122",
+BMGC_DS19799,BMG_DS077384,,"BLEEDING DISORDER, VASCULAR-TYPE",,,,,,,C5935577,,612456;620715,MONDO:0958229,"bleeding disorder, vascular-type",
+BMGC_DS19800,BMG_DS077385,,OROFACIODIGITAL SYNDROME XX,,,,,DOID:0060962,orofaciodigital syndrome XX,C5935578,,620718;610917,MONDO:0958230,orofaciodigital syndrome 20,
+BMGC_DS19801,BMG_DS077386,,"DEAFNESS, AUTOSOMAL DOMINANT 90",,,,,DOID:0070607,autosomal dominant nonsyndromic deafness 90,C5935579,,620722;606808,MONDO:0958232,"hearing loss, autosomal dominant 90",
+BMGC_DS19802,BMG_DS077387,,BETHLEM MYOPATHY 1B,,,,,,,C5935580,,620725,MONDO:0958233,Bethlem myopathy 1B,
+BMGC_DS19803,BMG_DS077388,,BETHLEM MYOPATHY 1C,,,,,,,C5935581,,620726,MONDO:0958234,Bethlem myopathy 1C,
+BMGC_DS19804,BMG_DS077389,,ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1B,,,,,DOID:0060942,Ullrich congenital muscular dystrophy 1B,C5935582,,620727,MONDO:0958235,Ullrich congenital muscular dystrophy 1B,
+BMGC_DS19805,BMG_DS077390,,ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1C,,,,,DOID:0060943,Ullrich congenital muscular dystrophy 1C,C5935583,,620728,MONDO:0958236,Ullrich congenital muscular dystrophy 1C,
+BMGC_DS19806,BMG_DS077391,,MICROPHTHALMIA/COLOBOMA 11,,,,,,,C5935584,,601723;620731,MONDO:0958239,microphthalmia/coloboma 11,
+BMGC_DS19807,BMG_DS077392,,"NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS, SEIZURES, AND STRUCTURAL BRAIN ABNORMALITIES",,,,,,,C5935585,,609763;620732,MONDO:0958240,"neurodevelopmental disorder with hyperkinetic movements, seizures, and structural brain abnormalities",
+BMGC_DS19808,BMG_DS077393,,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 30, ATRIAL",,,,,,,C5935586,,605236;620734,MONDO:0958241,"cardiomyopathy, familial hypertrophic, 30, atrial",
+BMGC_DS19809,BMG_DS077394,,SPERMATOGENIC FAILURE 90,,,,,DOID:0070589,spermatogenic failure 90,C5935587,,620744;620377,MONDO:0958242,spermatogenic failure 90,
+BMGC_DS19810,BMG_DS077395,,"DEAFNESS, AUTOSOMAL RECESSIVE 123",,,,,,,C5935588,,186591;620745,MONDO:0958277,"hearing loss, autosomal recessive 123",
+BMGC_DS19811,BMG_DS077396,,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CHARACTERISTIC BRAIN ABNORMALITIES,,,,,,,C5935589,,605556;620746,MONDO:0958278,neurodevelopmental disorder with hypotonia and characteristic brain abnormalities,
+BMGC_DS19812,BMG_DS077397,,NEURODEVELOPMENTAL DISORDER WITH EARLY-ONSET PARKINSONISM AND BEHAVIORAL ABNORMALITIES,,,,,,,C5935590,,617342;620747,MONDO:0958323,neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities,
+BMGC_DS19813,BMG_DS077398,,MEGALENCEPHALY-POLYDACTYLY SYNDROME,,,,,,,C5935591,,620748;164840,MONDO:0958279,megalencephaly-polydactyly syndrome,
+BMGC_DS19814,BMG_DS077399,,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 12",,,,,,,C5935592,,620755;616440,MONDO:0958324,"generalized epilepsy with febrile seizures plus, type 12",
+BMGC_DS19815,BMG_DS077400,,THROMBOCYTOPENIA 12 WITH OR WITHOUT MYOPATHY,,,,,,,C5935593,,620757,MONDO:0958325,thrombocytopenia 12 with or without myopathy,
+BMGC_DS19816,BMG_DS077401,,MACULAR DYSTROPHY WITH OR WITHOUT CONE DYSFUNCTION,,,,,,,C5935594,,620493;620762,MONDO:0958326,macular dystrophy with or without cone dysfunction,
+BMGC_DS19817,BMG_DS077402,,SECKEL SYNDROME 11,,,,,,,C5935595,,617728;620767,MONDO:0958328,Seckel syndrome 11,
+BMGC_DS19818,BMG_DS077403,,JEFFRIES-LAKHANI NEURODEVELOPMENTAL SYNDROME,,,,,,,C5935596,,607170;620771,MONDO:0958329,Jeffries-Lakhani neurodevelopmental syndrome,
+BMGC_DS19819,BMG_DS077404,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 113,,,,,,,C5935597,,185860;620772,MONDO:0958330,developmental and epileptic encephalopathy 113,
+BMGC_DS19820,BMG_DS077405,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 114,,,,,,,C5935598,,620774;616440,MONDO:0958331,developmental and epileptic encephalopathy 114,
+BMGC_DS19821,BMG_DS077406,,"THROMBOCYTOPENIA 13, SYNDROMIC",,,,,,,C5935599,,606953;620776,MONDO:0958333,"thrombocytopenia 13, syndromic",
+BMGC_DS19822,BMG_DS077407,,"PULMONARY HYPERTENSION, PRIMARY, 6",,,,,,,C5935600,,114170;620777,MONDO:0958334,"pulmonary hypertension, primary, 6",
+BMGC_DS19823,BMG_DS077408,,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 82",,,,,DOID:0060947,autosomal recessive intellectual developmental disorder 82,C5935601,,617199;620779,MONDO:0968944,"intellectual developmental disorder, autosomal recessive 82",
+BMGC_DS19824,BMG_DS077409,,"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE ID",,,,,,,C5935602,,620780;601548,MONDO:0958335,"cutis laxa, autosomal recessive, type 1d",
+BMGC_DS19825,BMG_DS077410,,"NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT, AUTISM, AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER",,,,,,,C5935603,,620782;601178,MONDO:0968945,"neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder",
+BMGC_DS19826,BMG_DS077411,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 115,,,,,,,C5935604,,610904;620783,MONDO:0968946,developmental and epileptic encephalopathy 115,
+BMGC_DS19827,BMG_DS077412,,NEURODEVELOPMENTAL DISORDER PLUS OPTIC ATROPHY,,,,,,,C5935605,,610904;620784,MONDO:0968947,neurodevelopmental disorder plus optic atrophy,
+BMGC_DS19828,BMG_DS077413,,NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MOVEMENT ABNORMALITIES,,,,,,,C5935606,,616352;620785,MONDO:0968976,neurodevelopmental disorder with progressive movement abnormalities,
+BMGC_DS19829,BMG_DS077414,,"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 9, AUTOSOMAL RECESSIVE",,,,,,,C5935607,,614246;620786,MONDO:0968977,"basal ganglia calcification, idiopathic, 9, autosomal recessive",
+BMGC_DS19830,BMG_DS077415,,APLASIA CUTIS-ENAMEL DYSPLASIA SYNDROME,,,,,,,C5935608,,620789;601575,MONDO:0968978,aplasia cutis-enamel dysplasia syndrome,
+BMGC_DS19831,BMG_DS077416,,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND SEIZURES,,,,,,,C5935609,,612024;620790,MONDO:0968979,neurodevelopmental disorder with hypotonia and seizures,
+BMGC_DS19832,BMG_DS077417,,OTOSCLEROSIS 12,,,,,,,C5935610,,603254;620792,MONDO:0968980,otosclerosis 12,
+BMGC_DS19833,BMG_DS077418,,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 29",,,,,,,C5935611,,607902;620793,MONDO:0971171,"muscular dystrophy, limb-girdle, autosomal recessive 29",
+BMGC_DS19834,BMG_DS077419,,"DEAFNESS, AUTOSOMAL RECESSIVE 124",,,,,,,C5935612,,620794;607843,MONDO:0968981,autosomal recessive nonsyndromic hearing loss 124,
+BMGC_DS19835,BMG_DS077420,,AUTOINFLAMMATION WITH EPISODIC FEVER AND IMMUNE DYSREGULATION,,,,,,,C5935613,,620795;611885,MONDO:0968982,autoinflammation with episodic fever and immune dysregulation,
+BMGC_DS19836,BMG_DS077421,,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 6,,,,,,,C5935614,,177045;620796,MONDO:0968983,proteasome-associated autoinflammatory syndrome 6,
+BMGC_DS19837,BMG_DS077422,,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 116,,,,,DOID:0070545,developmental and epileptic encephalopathy 116,C5935615,,138290;620806,MONDO:0970945,developmental and epileptic encephalopathy 116,
+BMGC_DS19838,BMG_DS077423,,IMMUNODEFICIENCY 121 WITH AUTOINFLAMMATION,,,,,,,C5935616,,176847;620807,MONDO:0971001,immunodeficiency 121 with autoinflammation,
+BMGC_DS19839,BMG_DS077424,,MHC CLASS I DEFICIENCY 2,,,,,,,C5935617,,620813;170261,MONDO:0971011,MHC class I deficiency 2,
+BMGC_DS19840,BMG_DS077425,,MHC CLASS I DEFICIENCY 3,,,,,,,C5935618,,620814,MONDO:0971012,MHC class I deficiency 3,
+BMGC_DS19841,BMG_DS077426,,"ROTHMUND-THOMSON SYNDROME, TYPE 4",,,,,,,C5935619,,601810;620819,MONDO:0970950,"Rothmund-Thomson syndrome, type 4",
+BMGC_DS19842,BMG_DS077427,,EL HAYEK-CHAHROUR NEURODEVELOPMENTAL SYNDROME,,,,,,,C5935620,,180202;620820,MONDO:0970951,El Hayek-Chahrour neurodevelopmental disorder,
+BMGC_DS19843,BMG_DS077428,,IMMUNODEFICIENCY 119,,,,,,,C5935621,,605717;620825,MONDO:0970993,immunodeficiency 119,
+BMGC_DS19844,BMG_DS077429,,IMMUNODEFICIENCY 120,,,,,,,C5935622,,620836;174761,MONDO:0970994,immunodeficiency 120,
+BMGC_DS19845,BMG_DS077430,,SPERMATOGENIC FAILURE 91,,,,,DOID:0070590,spermatogenic failure 91,C5935623,,620838;603960,MONDO:0970952,spermatogenic failure 91,
+BMGC_DS19846,BMG_DS077431,,PREMATURE OVARIAN FAILURE 24,,,,,,,C5935624,,616799;620840,MONDO:0970995,premature ovarian failure 24,
+BMGC_DS19847,BMG_DS077432,,SPERMATOGENIC FAILURE 92,,,,,DOID:0070591,spermatogenic failure 92,C5935625,,620708;620848,MONDO:0970999,spermatogenic failure 92,
+BMGC_DS19848,BMG_DS077433,,SPERMATOGENIC FAILURE 93,,,,,DOID:0070592,spermatogenic failure 93,C5935626,,607670;620849,MONDO:0971000,spermatogenic failure 93,
+BMGC_DS19849,BMG_DS077434,,SPERMATOGENIC FAILURE 94,,,,,DOID:0070593,spermatogenic failure 94,C5935627,,620850;619829,MONDO:0971002,spermatogenic failure 94,
+BMGC_DS19850,BMG_DS077435,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, BRAIN ANOMALIES, DISTINCTIVE FACIES, AND ABSENT LANGUAGE",,,,,,,C5935628,,620823;620851,MONDO:0971172,"neurodevelopmental disorder with hypotonia, brain anomalies, distinctive facies, and absent language",
+BMGC_DS19851,BMG_DS077436,,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FEEDING DIFFICULTIES, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES",,,,,,,C5935629,,604981;620852,MONDO:0971043,"neurodevelopmental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities",
+BMGC_DS19852,BMG_DS077437,,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL RECESSIVE 11, WITH SPASTICITY",,,,,,,C5935630,,620854;603183,MONDO:0971150,"neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity",
+BMGC_DS19853,BMG_DS077438,,"EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 3",,,,,,,C5935631,,620865;188061,MONDO:0971044,"Ehlers-Danlos syndrome, classic-like, 3",
+BMGC_DS19854,BMG_DS077439,,IMMUNODEFICIENCY 122,,,,,,,C5935632,,611415;620869,MONDO:0971151,immunodeficiency 122,
+BMGC_DS19855,BMG_DS077440,,"DEAFNESS, AUTOSOMAL RECESSIVE 125",,,,,,,C5935633,,602835;620877,MONDO:0971152,"hearing loss, autosomal recessive 125",
+BMGC_DS19856,BMG_DS077441,,AUTOINFLAMMATION WITH ARTHRITIS AND VASCULITIS,,,,,,,C5935634,,604834;620880,MONDO:0971173,autoinflammation with arthritis and vasculitis,
+BMGC_DS19857,BMG_DS077442,,MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 9B,,,,,,,C5935635,,103270;620887,MONDO:0971174,multiple mitochondrial dysfunctions syndrome 9b,
+BMGC_DS19858,BMG_DS077443,,"CARDIOMYOPATHY, DILATED, 2K",,,,,,,C5935636,,620894;614071,MONDO:0971175,"cardiomyopathy, dilated, 2K",
+BMGC_DS19859,BMG_DS077444,,OVARIAN DYSGENESIS 11,,,,,,,C5935637,,618611;620897,MONDO:0971176,ovarian dysgenesis 11,
+BMGC_DS19860,BMG_DS077445,,IMMUNODEFICIENCY 123 WITH HPV-RELATED VERRUCOSIS,,,,,,,C5935639,,186760;620901,MONDO:0971177,immunodeficiency 123 with HPV-related verrucosis,
+BMGC_DS19861,BMG_DS077446,,POLYCYSTIC KIDNEY DISEASE 8,,,,,,,C5935640,,609799;620903,MONDO:0971178,polycystic kidney disease 8,
+BMGC_DS19862,BMG_DS077447,,ARTERIAL TORTUOSITY-BONE FRAGILITY SYNDROME,,,,,,,C5935641,,130660;620908,MONDO:0971179,arterial tortuosity-bone fragility syndrome,
+BMGC_DS19863,BMG_DS077448,,OTOFACIAL NEURODEVELOPMENTAL SYNDROME,,,,,,,C5935642,,618365;620910,MONDO:0975705,otofacial neurodevelopmental syndrome,
+BMGC_DS19864,BMG_DS077449,,"NEUROMUSCULAR DISORDER, CONGENITAL, WITH DYSMORPHIC FACIES",,,,,,,C5935643,,607307;620775,MONDO:0958332,"neuromuscular disorder, congenital, with dysmorphic facies",
+BMGC_DS19865,BMG_DS077473,,SPINAL MUSCULAR ATROPHY WITH MICROCEPHALY AND IMPAIRED INTELLECTUAL DEVELOPMENT,,,,,,,C5935682,,271110,MONDO:0010055,spinal muscular atrophy with microcephaly and mental subnormality,
+BMGC_DS19866,BMG_DS077478,,Plica polonica,Hair Diseases,,,,,,C5940798,D006201,,,,
+BMGC_DS19867,BMG_DS077479,,ASM Deficiency,Niemann-Pick Diseases,,,,,,C5940804,D009542,,,,
+BMGC_DS19868,BMG_DS077480,,Fulminant Intracranial Hypertension,Pseudotumor Cerebri,,,,,,C5940805,D011559,,,,
+BMGC_DS19869,BMG_DS077481,,Secondary Intracranial Hypertension,Pseudotumor Cerebri,,,,,,C5940806,D011559,,,,
+BMGC_DS19870,BMG_DS077485,,,,,,,DOID:0080094,myofibrillar myopathy 3,,C000598645,,,,
+BMGC_DS19871,BMG_DS077486,,,,,,,DOID:0050096,tinea barbae,,C000656825,,,,
+BMGC_DS19872,BMG_DS077488,,,,,,,DOID:0060330,Rapp-Hodgkin syndrome,,C535289,,,,
+BMGC_DS19873,BMG_DS077489,,,,,,,DOID:0090016,chromosome 5q deletion syndrome,,C535323,,,,
+BMGC_DS19874,BMG_DS077490,,,,,,,DOID:0111597,distal arthrogryposis type 1A,,C535378,,,,
+BMGC_DS19875,BMG_DS077491,,,,,,,DOID:0050663,Bethlem myopathy,,C535436,,,,
+BMGC_DS19876,BMG_DS077492,,,,,,,DOID:0111955,immunodeficiency 27A,,C535530,,MONDO:0020530,Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency,
+BMGC_DS19877,BMG_DS077494,,,,,,,DOID:0060233,cardiofaciocutaneous syndrome,,C535579,,,,
+BMGC_DS19878,BMG_DS077495,,,,,,,DOID:0060409,NFIA-related disorder,,C535594,,,,
+BMGC_DS19879,BMG_DS077496,,,,,,,DOID:0060745,Doyne honeycomb retinal dystrophy,,C535602,,,,
+BMGC_DS19880,BMG_DS077497,,,,,,,DOID:0080050,"acromesomelic dysplasia, Maroteaux type",,C535661,,,,
+BMGC_DS19881,BMG_DS077498,,,,,,,DOID:0080150,adrenocorticotropic hormone deficiency,,C535668,,,,
+BMGC_DS19882,BMG_DS077499,,,,,,,DOID:0110633,rigid spine muscular dystrophy 1,,C535683,,MONDO:0019951,rigid spine syndrome,
+BMGC_DS19883,BMG_DS077500,,,,,,,DOID:14789,spondyloepiphyseal dysplasia congenita,,C535788,,,,
+BMGC_DS19884,BMG_DS077501,,,,,,,DOID:0050757,deafness-dystonia-optic neuronopathy syndrome,,C535808,,,,
+BMGC_DS19885,BMG_DS077502,,,,,,,DOID:0111165,molybdenum cofactor deficiency,,C535811,,,,
+BMGC_DS19886,BMG_DS077503,,,,,,,DOID:0080047,pseudoachondroplasia,,C535819,,,,
+BMGC_DS19887,BMG_DS077504,,,,,,,DOID:0111603,distal arthrogryposis type 7,,C535857,,,,
+BMGC_DS19888,BMG_DS077505,,,,,,,DOID:0080094,myofibrillar myopathy 3,,C535906,,,,
+BMGC_DS19889,BMG_DS077508,,,,,,,DOID:0080056,achondrogenesis type II,,C536017,,,,
+BMGC_DS19890,BMG_DS077509,,,,,,,DOID:0080153,medium chain acyl-CoA dehydrogenase deficiency,,C536038,,,,
+BMGC_DS19891,BMG_DS077510,,,,,,,,,,C536092,607948,MONDO:0000070,"Mycobacterium tuberculosis, susceptibility",
+BMGC_DS19892,BMG_DS077511,,,,,,,,,,C536201,,MONDO:0007526,"Ehlers-Danlos syndrome, spondylodysplastic type",
+BMGC_DS19893,BMG_DS077512,,,,,,,DOID:0060731,congenital central hypoventilation syndrome,,C536209,,,,
+BMGC_DS19894,BMG_DS077513,,,,,,,DOID:0110988,Joubert syndrome 2,,C536294,,,,
+BMGC_DS19895,BMG_DS077514,,,,,,,DOID:0110998,Joubert syndrome 3,,C536295,,,,
+BMGC_DS19896,BMG_DS077515,,,,,,,DOID:0080082,nonsyndromic congenital nail disorder 4,,C536377,,,,
+BMGC_DS19897,BMG_DS077516,,,,,,,DOID:0110950,Waardenburg syndrome type 2A,,C536464,,,,
+BMGC_DS19898,BMG_DS077517,,,,,,,,,,C536647,,MONDO:0008824,fetal akinesia deformation sequence,
+BMGC_DS19899,BMG_DS077518,,,,,,,DOID:0080696,Winchester syndrome,,C536709,,,,
+BMGC_DS19900,BMG_DS077519,,,,,,,DOID:0050946,Charlevoix-Saguenay spastic ataxia,,C536787,,,,
+BMGC_DS19901,BMG_DS077520,,,,,,,DOID:0111254,glutaric acidemia I,,C536833,,,,
+BMGC_DS19902,BMG_DS077521,,,,,,,DOID:0050547,familial medullary thyroid carcinoma,,C536911,,,,
+BMGC_DS19903,BMG_DS077522,,,,,,,DOID:0110070,arrhythmogenic right ventricular dysplasia 1,,C536932,,,,
+BMGC_DS19904,BMG_DS077523,,,,,,,DOID:0050887,Townes-Brocks syndrome,,C536974,,,,
+BMGC_DS19905,BMG_DS077524,,,,,,,DOID:0050631,Allan-Herndon-Dudley syndrome,,C537047,,,,
+BMGC_DS19906,BMG_DS077525,,,,,,,DOID:0110966,brachydactyly type A3,,C537090,,,,
+BMGC_DS19907,BMG_DS077526,,,,,,,DOID:0050694,Brown-Vialetto-Van Laere syndrome,,C537111,,,,
+BMGC_DS19908,BMG_DS077527,,,,,,,DOID:0080549,Noonan syndrome with multiple lentigines 2,,C537117,,,,
+BMGC_DS19909,BMG_DS077528,,,,,,,DOID:0050975,spinocerebellar ataxia type 26,,C537203,,,,
+BMGC_DS19910,BMG_DS077529,,,,,,,,,,C537268,,MONDO:0023176,formaldehyde poisoning,
+BMGC_DS19911,BMG_DS077530,,,,,,,DOID:0111607,distal arthrogryposis type 3,,C537288,,,,
+BMGC_DS19912,BMG_DS077533,,,,,,,DOID:0080799,sinonasal undifferentiated carcinoma,,C537344,,,,
+BMGC_DS19913,BMG_DS077534,,,,,,,,,,C537359,,MONDO:0016826,methylmalonic aciduria and homocystinuria,
+BMGC_DS19914,BMG_DS077535,,,,,,,DOID:0080110,"contractures, pterygia, and spondylocarpotarsal fusion syndrome",,C537377,,,,
+BMGC_DS19915,BMG_DS077536,,,,,,,DOID:0111808,linear skin defects with multiple congenital anomalies 1,,C537466,,MONDO:0010672,linear skin defects with multiple congenital anomalies,
+BMGC_DS19916,BMG_DS077537,,,,,,,DOID:0070013,Seckel syndrome 2,,C537534,,,,
+BMGC_DS19917,BMG_DS077539,,,,,,,DOID:0060608,microcephalic osteodysplastic primordial dwarfism type I,,C537577,,,,
+BMGC_DS19918,BMG_DS077540,,,,,,,DOID:0050659,biotin-responsive basal ganglia disease,,C537658,,,,
+BMGC_DS19919,BMG_DS077541,,,,,,,DOID:0111000,Joubert syndrome 5,,C537688,,,,
+BMGC_DS19920,BMG_DS077542,,,,,,,DOID:0111001,Joubert syndrome 6,,C537689,,,,
+BMGC_DS19921,BMG_DS077543,,,,,,,DOID:0060540,Hermansky-Pudlak syndrome 2,,C537709,,,,
+BMGC_DS19922,BMG_DS077546,,,,,,,DOID:0060581,Noonan syndrome 3,,C537847,,,,
+BMGC_DS19923,BMG_DS077547,,,,,,,,,,C537856,193003,MONDO:0008654,spinocerebellar ataxia 27A,
+BMGC_DS19924,BMG_DS077549,,,,,,,DOID:0060673,Peters anomaly,,C537884,,,,
+BMGC_DS19925,BMG_DS077550,,,,,,,DOID:8943,lattice corneal dystrophy,,C537935,,,,
+BMGC_DS19926,BMG_DS077551,,,,,,,DOID:0090056,dystonia 12,,C538001,,,,
+BMGC_DS19927,BMG_DS077553,,,,,,,DOID:0081044,frontonasal dysplasia,,C538065,,,,
+BMGC_DS19928,BMG_DS077554,,,,,,,,,,C538153,,MONDO:0000722,non-syndromic synpolydactyly,
+BMGC_DS19929,BMG_DS077555,,,,,,,DOID:0050678,Blau syndrome,,C538157,,,,
+BMGC_DS19930,BMG_DS077557,,,,,,,DOID:0110390,retinitis pigmentosa 1,,C538365,,,,
+BMGC_DS19931,BMG_DS077558,,,,,,,DOID:0110936,nemaline myopathy 5A,,C538397,,,,
+BMGC_DS19932,BMG_DS077559,,,,,,,DOID:0111599,distal arthrogryposis type 2B,,C538400,,,,
+BMGC_DS19933,BMG_DS077560,,,,,,,,,,C562440,241510,MONDO:0009428,obsolete childhood hypophosphatasia,
+BMGC_DS19934,BMG_DS077563,,,,,,,DOID:0050159,lymphoid interstitial pneumonia,,C562489,,,,
+BMGC_DS19935,BMG_DS077566,,,,,,,DOID:0070338,cerebellar hypoplasia,,C562568,,,,
+BMGC_DS19936,BMG_DS077567,,,,,,,DOID:0111347,epidermolysis bullosa with congenital localized absence of skin and deformity of nails,,C562638,,,,
+BMGC_DS19937,BMG_DS077568,,,,,,,DOID:0050630,Aland Island eye disease,,C562664,,,,
+BMGC_DS19938,BMG_DS077569,,,,,,,,,,C562725,612423,MONDO:0012901,inherited prekallikrein deficiency,
+BMGC_DS19939,BMG_DS077571,,,,,,,DOID:0110002,3-methylglutaconic aciduria type 1,,C562801,,,,
+BMGC_DS19940,BMG_DS077572,,,,,,,DOID:0080032,craniodiaphyseal dysplasia,,C562940,,,,
+BMGC_DS19941,BMG_DS077573,,,,,,,DOID:0110214,cleft soft palate,,C562950,,,,
+BMGC_DS19942,BMG_DS077574,,,,,,,DOID:0050577,cranioectodermal dysplasia,,C562966,,,,
+BMGC_DS19943,BMG_DS077575,,,,,,,DOID:0080044,hypochondrogenesis,,C563007,,,,
+BMGC_DS19944,BMG_DS077576,,,,,,,DOID:0111144,preterm premature rupture of the membranes,,C563032,,,,
+BMGC_DS19945,BMG_DS077577,,,,,,,DOID:0060746,basal laminar drusen,,C563034,,,,
+BMGC_DS19946,BMG_DS077578,,,,,,,DOID:0060680,pigment dispersion syndrome,,C563184,,,,
+BMGC_DS19947,BMG_DS077579,,,,,,,DOID:0112186,thyroid dyshormonogenesis 2A,,C563206,,,,
+BMGC_DS19948,BMG_DS077580,,,,,,,DOID:14766,renal agenesis,,C563261,,,,
+BMGC_DS19949,BMG_DS077581,,,,,,,DOID:0110900,inflammatory bowel disease 2,,C563310,,,,
+BMGC_DS19950,BMG_DS077582,,,,,,,,,,C563362,607801,MONDO:0011910,obsolete autosomal dominant limb-girdle muscular dystrophy type 1C,
+BMGC_DS19951,BMG_DS077583,,,,,,,DOID:0060694,Cayman type cerebellar ataxia,,C563363,,,,
+BMGC_DS19952,BMG_DS077584,,,,,,,DOID:0080397,orofacial cleft 3,,C563448,,,,
+BMGC_DS19953,BMG_DS077585,,,,,,,DOID:0080400,orofacial cleft 7,,C563464,,,,
+BMGC_DS19954,BMG_DS077586,,,,,,,DOID:0050881,inclusion body myopathy with Paget disease of bone and frontotemporal dementia,,C563476,,,,
+BMGC_DS19955,BMG_DS077587,,,,,,,DOID:0060403,chromosome 17q11.2 deletion syndrome,,C563524,,,,
+BMGC_DS19956,BMG_DS077588,,,,,,,DOID:0110397,retinitis pigmentosa 27,,C563526,,,,
+BMGC_DS19957,BMG_DS077589,,,,,,,DOID:0110876,holoprosencephaly 7,,C563660,,,,
+BMGC_DS19958,BMG_DS077590,,,,,,,DOID:0080399,orofacial cleft 5,,C563843,,,,
+BMGC_DS19959,BMG_DS077591,,,,,,,DOID:0110886,inflammatory bowel disease 9,,C563926,,,,
+BMGC_DS19960,BMG_DS077592,,,,,,,,,,C564135;C567925,146840;147060,MONDO:0007818,"hyper-IgE recurrent infection syndrome 1, autosomal dominant",
+BMGC_DS19961,BMG_DS077593,,,,,,,DOID:0110216,Leber congenital amaurosis 11,,C564140,,,,
+BMGC_DS19962,BMG_DS077595,,,,,,,DOID:0110875,holoprosencephaly 3,,C564181,,,,
+BMGC_DS19963,BMG_DS077596,,,,,,,DOID:0110010,achromatopsia 4,,C564206,,,,
+BMGC_DS19964,BMG_DS077597,,,,,,,DOID:0110406,retinitis pigmentosa 30,,C564310,,,,
+BMGC_DS19965,BMG_DS077598,,,,,,,DOID:0111361,hypotrichosis-lymphedema-telangiectasia syndrome,,C564327,,,,
+BMGC_DS19966,BMG_DS077599,,,,,,,DOID:0112174,combined deficiency of vitamin K-dependent clotting factors 2,,C564393,,,,
+BMGC_DS19967,BMG_DS077600,,,,,,,,,,C564424,305690,MONDO:0010594,obsolete inherited genitourinary tract anomalies,
+BMGC_DS19968,BMG_DS077601,,,,,,,DOID:0110414,retinitis pigmentosa 3,,C564520,,,,
+BMGC_DS19969,BMG_DS077602,,,,,,,DOID:0112148,Uruguay faciocardiomusculoskeletal syndrome,,C564544,,,,
+BMGC_DS19970,BMG_DS077604,,,,,,,DOID:0111017,cone-rod dystrophy 10,,C564597,,,,
+BMGC_DS19971,BMG_DS077605,,,,,,,DOID:0111115,nephronophthisis 4,,C564640,,,,
+BMGC_DS19972,BMG_DS077606,,,,,,,DOID:0080533,Carney-Stratakis syndrome,,C564650,,,,
+BMGC_DS19973,BMG_DS077607,,,,,,,DOID:0110903,inflammatory bowel disease 4,,C564680,,,,
+BMGC_DS19974,BMG_DS077608,,,,,,,DOID:0110907,inflammatory bowel disease 6,,C564681,,,,
+BMGC_DS19975,BMG_DS077609,,,,,,,DOID:0110904,inflammatory bowel disease 8,,C564682,,,,
+BMGC_DS19976,BMG_DS077610,,,,,,,DOID:0111077,congenital nonspherocytic hemolytic anemia 2,,C564858,,,,
+BMGC_DS19977,BMG_DS077612,,,,,,,,,,C565071,129150,MONDO:0007506,obsoleted echo virus 11 sensitivity,
+BMGC_DS19978,BMG_DS077613,,,,,,,DOID:0081109,keratosis palmoplantaris striata 2,,C565102,,,,
+BMGC_DS19979,BMG_DS077614,,,,,,,DOID:0060297,complement component 4a deficiency,,C565167,,,,
+BMGC_DS19980,BMG_DS077615,,,,,,,DOID:0080914,cerebrooculofacioskeletal syndrome 4,,C565184,,,,
+BMGC_DS19981,BMG_DS077616,,,,,,,DOID:0050689,brachydactyly-syndactyly syndrome,,C565193,,,,
+BMGC_DS19982,BMG_DS077617,,,,,,,DOID:0110357,retinitis pigmentosa 35,,C565206,,,,
+BMGC_DS19983,BMG_DS077618,,,,,,,DOID:0110889,inflammatory bowel disease 5,,C565234,,,,
+BMGC_DS19984,BMG_DS077619,,,,,,,DOID:0111409,exudative vitreoretinopathy 3,,C565297,,,,
+BMGC_DS19985,BMG_DS077621,,,,,,,DOID:0060867,macrocephaly-autism syndrome,,C565342,,,,
+BMGC_DS19986,BMG_DS077622,,,,,,,DOID:0110882,inflammatory bowel disease 7,,C565353,,,,
+BMGC_DS19987,BMG_DS077623,,,,,,,DOID:0060245,Mast syndrome,,C565409,,,,
+BMGC_DS19988,BMG_DS077624,,,,,,,DOID:0111355,hydrolethalus syndrome 1,,C565504,,,,
+BMGC_DS19989,BMG_DS077625,,,,,,,DOID:0111218,Friedreich ataxia 1,,C565561,,,,
+BMGC_DS19990,BMG_DS077627,,,,,,,DOID:0110630,Wolfram syndrome 2,,C565733,,,,
+BMGC_DS19991,BMG_DS077628,,,,,,,DOID:0110128,Bardet-Biedl syndrome 6,,C565738,,,,
+BMGC_DS19992,BMG_DS077629,,,,,,,DOID:0110891,inflammatory bowel disease 3,,C565764,,,,
+BMGC_DS19993,BMG_DS077630,,,,,,,DOID:0111114,nephronophthisis 3,,C565780,,,,
+BMGC_DS19994,BMG_DS077631,,,,,,,DOID:0111129,focal segmental glomerulosclerosis 2,,C565831,,,,
+BMGC_DS19995,BMG_DS077632,,,,,,,DOID:0110646,long QT syndrome 3,,C565840,,,,
+BMGC_DS19996,BMG_DS077633,,,,,,,DOID:0110129,Bardet-Biedl syndrome 7,,C565916,,,,
+BMGC_DS19997,BMG_DS077634,,,,,,,DOID:0110130,Bardet-Biedl syndrome 8,,C565917,,,,
+BMGC_DS19998,BMG_DS077635,,,,,,,DOID:0110131,Bardet-Biedl syndrome 9,,C565918,,,,
+BMGC_DS19999,BMG_DS077636,,,,,,,DOID:0110132,Bardet-Biedl syndrome 10,,C565919,,,,
+BMGC_DS20000,BMG_DS077637,,,,,,,DOID:0110133,Bardet-Biedl syndrome 11,,C565920,,,,
+BMGC_DS20001,BMG_DS077638,,,,,,,DOID:0110134,Bardet-Biedl syndrome 12,,C565921,,,,
+BMGC_DS20002,BMG_DS077639,,,,,,,DOID:0060689,atrichia with papular lesions,,C565924,,,,
+BMGC_DS20003,BMG_DS077640,,,,,,,DOID:0050645,arterial tortuosity syndrome,,C565942,,,,
+BMGC_DS20004,BMG_DS077642,,,,,,,DOID:0111593,distal arthrogryposis type 10,,C566069,,,,
+BMGC_DS20005,BMG_DS077643,,,,,,,DOID:0080395,orofacial cleft 1,,C566121,,,,
+BMGC_DS20006,BMG_DS077644,,,,,,,DOID:0060342,acromelic frontonasal dysostosis,,C566345,,,,
+BMGC_DS20007,BMG_DS077645,,,,,,,DOID:0080396,orofacial cleft 2,,C566419,,,,
+BMGC_DS20008,BMG_DS077646,,,,,,,DOID:0110405,retinitis pigmentosa 36,,C566431,,,,
+BMGC_DS20009,BMG_DS077647,,,,,,,DOID:0110878,holoprosencephaly 5,,C566464,,,,
+BMGC_DS20010,BMG_DS077648,,,,,,,DOID:0081023,retinal cone dystrophy 4,,C566470,,,,
+BMGC_DS20011,BMG_DS077649,,,,,,,DOID:0111113,nephronophthisis 2,,C566582,,,,
+BMGC_DS20012,BMG_DS077650,,,,,,,DOID:0111219,Friedreich ataxia 2,,C566594,,,,
+BMGC_DS20013,BMG_DS077651,,,,,,,DOID:0080403,orofacial cleft 10,,C566605,,,,
+BMGC_DS20014,BMG_DS077652,,,,,,,DOID:0110354,retinitis pigmentosa 19,,C566637,,,,
+BMGC_DS20015,BMG_DS077653,,,,,,,DOID:0110387,retinitis pigmentosa 9,,C566716,,,,
+BMGC_DS20016,BMG_DS077654,,,,,,,DOID:0081024,retinal cone dystrophy 1,,C566719,,,,
+BMGC_DS20017,BMG_DS077656,,,,,,,,,,C566740,178000,MONDO:0008337,familial pterygium of the conjunctiva,
+BMGC_DS20018,BMG_DS077657,,,,,,,DOID:0110647,long QT syndrome 5,,C566766,,,,
+BMGC_DS20019,BMG_DS077658,,,,,,,DOID:0060563,Char syndrome,,C566815,,,,
+BMGC_DS20020,BMG_DS077659,,,,,,,,,,C566826,,MONDO:0018953,parietal foramina,
+BMGC_DS20021,BMG_DS077660,,,,,,,DOID:0080205,CAKUT,,C566906,,,,
+BMGC_DS20022,BMG_DS077661,,,,,,,DOID:0111002,Joubert syndrome 7,,C566916,,,,
+BMGC_DS20023,BMG_DS077662,,,,,,,DOID:0111116,nephronophthisis 7,,C566930,,,,
+BMGC_DS20024,BMG_DS077663,,,,,,,DOID:0080137,multiple endocrine neoplasia type 4,,C567059,,,,
+BMGC_DS20025,BMG_DS077664,,,,,,,DOID:0080666,warfarin sensitivity,,C567080,,,,
+BMGC_DS20026,BMG_DS077665,,,,,,,DOID:0110135,Bardet-Biedl syndrome 13,,C567140,,,,
+BMGC_DS20027,BMG_DS077667,,,,,,,DOID:0110330,Leber congenital amaurosis 13,,C567197,,,,
+BMGC_DS20028,BMG_DS077668,,,,,,,DOID:0080404,orofacial cleft 11,,C567410,,,,
+BMGC_DS20029,BMG_DS077669,,,,,,,DOID:0090048,dystonia 16,,C567430,,,,
+BMGC_DS20030,BMG_DS077670,,,,,,,DOID:0050662,bestrophinopathy,,C567518,,,,
+BMGC_DS20031,BMG_DS077672,,,,,,,DOID:0050812,"spondyloepimetaphyseal dysplasia, Pakistani type",,C567551,,,,
+BMGC_DS20032,BMG_DS077673,,,,,,,DOID:0080124,mitochondrial DNA depletion syndrome 5,,C567624,,,,
+BMGC_DS20033,BMG_DS077674,,,,,,,DOID:0060900,Parkinson's disease 14,,C567844,,,,
+BMGC_DS20034,BMG_DS077675,,,,,,,DOID:0110386,retinitis pigmentosa 42,,C567854,,,,
+BMGC_DS20035,BMG_DS077676,,,,,,,DOID:0111771,"46,XY sex reversal 4",,C567887,,,,
+BMGC_DS20036,BMG_DS077677,,,,,,,DOID:0050160,inhalation anthrax,,C571912,,,,
+BMGC_DS20037,BMG_DS077679,,,,,,,DOID:0080043,achondrogenesis,,C579878,,,,
+BMGC_DS20038,BMG_DS077680,,,,,,,DOID:0111227,frontotemporal dementia and/or amyotrophic lateral sclerosis 7,,C579991,,,,
+BMGC_DS20039,BMG_DS077682,,,,,,,DOID:0090110,immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome,,C580192,,,,
+BMGC_DS20040,BMG_DS077683,,,,,,,DOID:14764,Larsen syndrome,,C580241,,,,
+BMGC_DS20041,BMG_DS077684,,,,,,,DOID:0080124,mitochondrial DNA depletion syndrome 5,,C580473,,,,
+BMGC_DS20042,BMG_DS077686,,,"Abdomen, Acute",,,,,,,D000006,,,,
+BMGC_DS20043,BMG_DS077688,,,Abdominal Neoplasms,,,,,,,D000008,,,,
+BMGC_DS20044,BMG_DS077689,,,Congenital Abnormalities,,,,,,,D000013,,MONDO:0000839,obsolete congenital abnormality,
+BMGC_DS20045,BMG_DS077690,,,"Abnormalities, Drug-Induced",,,,,,,D000014,,,,
+BMGC_DS20046,BMG_DS077691,,,"Abnormalities, Multiple",,,,,,,D000015,,,,
+BMGC_DS20047,BMG_DS077693,,,"Abortion, Spontaneous",,,,,,,D000022,,,,
+BMGC_DS20048,BMG_DS077697,,,"Abortion, Threatened",,,,,,,D000033,,,,
+BMGC_DS20049,BMG_DS077698,,,Abruptio Placentae,,,,,,,D000037,,,,
+BMGC_DS20050,BMG_DS077708,,,,,,,DOID:0060041,autism spectrum disorder,,D000067877,,,,
+BMGC_DS20051,BMG_DS077723,,,Anterior Cruciate Ligament Injuries,,,,,,,D000070598,,,,
+BMGC_DS20052,BMG_DS077729,,,"Brain Injuries, Diffuse",,,,,,,D000070625,,,,
+BMGC_DS20053,BMG_DS077731,,,"Brain Injuries, Traumatic",,,,,,,D000070642,,,,
+BMGC_DS20054,BMG_DS077735,,,Hyperekplexia,,,,DOID:0060696;DOID:0060695,hyperekplexia | hyperekplexia 1,,D000071017,,,,
+BMGC_DS20055,BMG_DS077736,,,Anorectal Malformations,,,,,,,D000071056,,,,
+BMGC_DS20056,BMG_DS077752,,,ST Elevation Myocardial Infarction,,,,,,,D000072657,,MONDO:0041656,ST-elevation myocardial infarction,
+BMGC_DS20057,BMG_DS077753,,,Ciliopathies,,,,,,,D000072661,,,,
+BMGC_DS20058,BMG_DS077756,,,Ankyloglossia,,,,DOID:0060604,ankyloglossia,,D000072676,,,,
+BMGC_DS20059,BMG_DS077757,,,Cancer Pain,,,,,,,D000072716,,,,
+BMGC_DS20060,BMG_DS077768,,,Meconium Ileus,,,,,,,D000074270,,,,
+BMGC_DS20061,BMG_DS077769,,,Opium Dependence,,,,,,,D000074607,,,,
+BMGC_DS20062,BMG_DS077773,,,Cardiac Conduction System Disease,,,,,,,D000075224,,,,
+BMGC_DS20063,BMG_DS077774,,,Heavy Metal Poisoning,,,,,,,D000075322,,MONDO:0023305,heavy metal poisoning,
+BMGC_DS20064,BMG_DS077775,,,Immunoglobulin Light-chain Amyloidosis,,,,DOID:0080933,immunoglobulin light chain amyloidosis,,D000075363,,,,
+BMGC_DS20065,BMG_DS077778,,,Clinical Deterioration,,,,,,,D000075902,,,,
+BMGC_DS20066,BMG_DS077780,,,Drug Misuse,,,,,,,D000076064,,,,
+BMGC_DS20067,BMG_DS077782,,,Adenocarcinoma of Lung,,,,,,,D000077192,,,,
+BMGC_DS20068,BMG_DS077783,,,Squamous Cell Carcinoma of Head and Neck,,,,,,,D000077195,,,,
+BMGC_DS20069,BMG_DS077785,,,"Carcinoma, Ovarian Epithelial",,,,,,,D000077216,,,,
+BMGC_DS20070,BMG_DS077786,,,Sleepiness,,,,,,,D000077260,,,,
+BMGC_DS20071,BMG_DS077787,,,"Thyroid Cancer, Papillary",,,,,,,D000077273,,,,
+BMGC_DS20072,BMG_DS077788,,,Nasopharyngeal Carcinoma,,,,,,,D000077274,,,,
+BMGC_DS20073,BMG_DS077789,,,Esophageal Squamous Cell Carcinoma,,,,,,,D000077277,,,,
+BMGC_DS20074,BMG_DS077793,,,Body-Weight Trajectory,,,,,,,D000077962,,,,
+BMGC_DS20075,BMG_DS077794,,,Gestational Weight Gain,,,,,,,D000078064,,,,
+BMGC_DS20076,BMG_DS077812,,,Shwachman-Diamond Syndrome,,,,DOID:0060479,Shwachman-Diamond syndrome,,D000081003,,,,
+BMGC_DS20077,BMG_DS077813,,,Ototoxicity,,,,,,,D000081015,,,,
+BMGC_DS20078,BMG_DS077814,,,Pulmonary Arterial Hypertension,,,,,,,D000081029,,,,
+BMGC_DS20079,BMG_DS077832,,,Chemotherapy-Related Cognitive Impairment,,,,,,,D000084202,,,,
+BMGC_DS20080,BMG_DS077833,,,Hyperthermia,,,,,,,D000084462,,,,
+BMGC_DS20081,BMG_DS077834,,,"Mesothelioma, Malignant",,,,,,,D000086002,,,,
+BMGC_DS20082,BMG_DS077835,,,Anosmia,,,,,,,D000086582,,,,
+BMGC_DS20083,BMG_DS077836,,,Rhinorrhea,,,,,,,D000086722,,,,
+BMGC_DS20084,BMG_DS077876,,,"Melanoma, Cutaneous Malignant",,,,,,,D000096142,,,,
+BMGC_DS20085,BMG_DS077890,,,Uveal Melanoma,,,,,,,D000098943,,,,
+BMGC_DS20086,BMG_DS077899,,,Achondroplasia,,,,,,,D000130,,,,
+BMGC_DS20087,BMG_DS077900,,,Acid-Base Imbalance,,,,,,,D000137,,,,
+BMGC_DS20088,BMG_DS077901,,,Acidosis,,,,,,,D000138,,,,
+BMGC_DS20089,BMG_DS077902,,,Acrodynia,,,,,,,D000170,,MONDO:0016588,infantile mercury poisoning,
+BMGC_DS20090,BMG_DS077904,,,Acute-Phase Reaction,,,,,,,D000210,,,,
+BMGC_DS20091,BMG_DS077905,,,Adenocarcinoma,,,,,,,D000230,,,,
+BMGC_DS20092,BMG_DS077909,,,Adenoma,,,,,,,D000236,,,,
+BMGC_DS20093,BMG_DS077912,,,"Adenoma, Acidophil",,,,,,,D000239,,,,
+BMGC_DS20094,BMG_DS077913,,,Tissue Adhesions,,,,,,,D000267,,,,
+BMGC_DS20095,BMG_DS077914,,,Adrenal Cortex Neoplasms,,,,,,,D000306,,,,
+BMGC_DS20096,BMG_DS077915,,,Adrenal Insufficiency,,,,,,,D000309,,,,
+BMGC_DS20097,BMG_DS077916,,,Adrenal Gland Neoplasms,,,,,,,D000310,,,,
+BMGC_DS20098,BMG_DS077917,,,"Adrenal Hyperplasia, Congenital",,,,,,,D000312,,,,
+BMGC_DS20099,BMG_DS077921,,,Ageusia,,,,,,,D000370,,,,
+BMGC_DS20100,BMG_DS077925,,,Albuminuria,,,,,,,D000419,,,,
+BMGC_DS20101,BMG_DS077927,,,Alcoholic Intoxication,,,,,,,D000435,,,,
+BMGC_DS20102,BMG_DS077928,,,Alcoholism,,,,,,,D000437,,,,
+BMGC_DS20103,BMG_DS077929,,,"Alkalosis, Respiratory",,,,,,,D000472,,,,
+BMGC_DS20104,BMG_DS077930,,,"Alveolitis, Extrinsic Allergic",,,,,,,D000542,,,,
+BMGC_DS20105,BMG_DS077931,,,Ameloblastoma,,,,DOID:0050894,ameloblastoma,,D000564,,,,
+BMGC_DS20106,BMG_DS077932,,,Amelogenesis Imperfecta,,,,,,,D000567,,,,
+BMGC_DS20107,BMG_DS077933,,,Amenorrhea,,,,,,,D000568,,,,
+BMGC_DS20108,BMG_DS077934,,,Amnesia,,,,,,,D000647,,,,
+BMGC_DS20109,BMG_DS077935,,,"Amnesia, Retrograde",,,,,,,D000648,,,,
+BMGC_DS20110,BMG_DS077938,,,Anaphylaxis,,,,,,,D000707,,,,
+BMGC_DS20111,BMG_DS077939,,,Anaplasia,,,,,,,D000708,,,,
+BMGC_DS20112,BMG_DS077940,,,"Anemia, Dyserythropoietic, Congenital",,,,,,,D000742,,,,
+BMGC_DS20113,BMG_DS077941,,,"Anemia, Hypochromic",,,,,,,D000747,,,,
+BMGC_DS20114,BMG_DS077942,,,"Anemia, Refractory",,,,,,,D000753,,,,
+BMGC_DS20115,BMG_DS077943,,,"Anemia, Refractory, with Excess of Blasts",,,,,,,D000754,,,,
+BMGC_DS20116,BMG_DS077944,,,"Anemia, Sideroblastic",,,,,,,D000756,,,,
+BMGC_DS20117,BMG_DS077945,,,Anencephaly,,,,DOID:0060668,anencephaly,,D000757,,,,
+BMGC_DS20118,BMG_DS077946,,,Aneuploidy,,,,,,,D000782,,,,
+BMGC_DS20119,BMG_DS077947,,,Aneurysm,,,,,,,D000783,,,,
+BMGC_DS20120,BMG_DS077948,,,Aortic Dissection,,,,,,,D000784,,,,
+BMGC_DS20121,BMG_DS077949,,,Angina Pectoris,,,,,,,D000787,,,,
+BMGC_DS20122,BMG_DS077950,,,Angiokeratoma,,,,,,,D000794,,,,
+BMGC_DS20123,BMG_DS077951,,,Angioedema,,,,,,,D000799,,,,
+BMGC_DS20124,BMG_DS077952,,,Aniseikonia,,,,DOID:0050304,aniseikonia,,D000839,,,,
+BMGC_DS20125,BMG_DS077953,,,Ankylosis,,,,,,,D000844,,,,
+BMGC_DS20126,BMG_DS077954,,,Anodontia,,,,,,,D000848,,,,
+BMGC_DS20127,BMG_DS077956,,,Anophthalmos,,,,,,,D000853,,,,
+BMGC_DS20128,BMG_DS077957,,,Hypoxia,,,,,,,D000860,,,,
+BMGC_DS20129,BMG_DS077958,,,Anthrax,,,,,,,D000881,,,,
+BMGC_DS20130,BMG_DS077959,,,Anus Neoplasms,,,,,,,D001005,,,,
+BMGC_DS20131,BMG_DS077960,,,"Anus, Imperforate",,,,,,,D001006,,,,
+BMGC_DS20132,BMG_DS077961,,,Aortic Coarctation,,,,,,,D001017,,,,
+BMGC_DS20133,BMG_DS077962,,,"Aortic Stenosis, Subvalvular",,,,,,,D001020,,,,
+BMGC_DS20134,BMG_DS077963,,,Aortic Valve Stenosis,,,,,,,D001024,,,,
+BMGC_DS20135,BMG_DS077964,,,Aortopulmonary Septal Defect,,,,,,,D001028,,,,
+BMGC_DS20136,BMG_DS077969,,,Aphonia,,,,,,,D001044,,,,
+BMGC_DS20137,BMG_DS077970,,,Apnea,,,,,,,D001049,,,,
+BMGC_DS20138,BMG_DS077974,,,Argyria,,,,,,,D001129,,MONDO:0018952,argyria,
+BMGC_DS20139,BMG_DS077976,,,Arnold-Chiari Malformation,,,,,,,D001139,,,,
+BMGC_DS20140,BMG_DS077977,,,"Arrhythmia, Sinus",,,,,,,D001146,,,,
+BMGC_DS20141,BMG_DS077980,,,Arteriovenous Malformations,,,,,,,D001165,,MONDO:0016234,obsolete rare arteriovenous malformation,
+BMGC_DS20142,BMG_DS077981,,,Arteritis,,,,,,,D001167,,,,
+BMGC_DS20143,BMG_DS077982,,,"Arthritis, Experimental",,,,,,,D001169,,,,
+BMGC_DS20144,BMG_DS077983,,,Arthrogryposis,,,,,,,D001176,,MONDO:0015225,arthrogryposis syndrome,
+BMGC_DS20145,BMG_DS077986,,,Asphyxia,,,,,,,D001237,,,,
+BMGC_DS20146,BMG_DS077987,,,Asthenia,,,,,,,D001247,,,,
+BMGC_DS20147,BMG_DS077989,,,Astrocytoma,,,,,,,D001254,,,,
+BMGC_DS20148,BMG_DS077991,,,Atrial Flutter,,,,,,,D001282,,,,
+BMGC_DS20149,BMG_DS077992,,,Atrophy,,,,,,,D001284,,,,
+BMGC_DS20150,BMG_DS077993,,,Auditory Perceptual Disorders,,,,,,,D001308,,,,
+BMGC_DS20151,BMG_DS077997,,,Bacteriuria,,,,,,,D001437,,,,
+BMGC_DS20152,BMG_DS077999,,,Basal Cell Nevus Syndrome,,,,,,,D001478,,,,
+BMGC_DS20153,BMG_DS078000,,,,,,,,,,D001523,,MONDO:0002025,psychiatric disorder,
+BMGC_DS20154,BMG_DS078002,,,Bile Duct Neoplasms,,,,,,,D001650,,,,
+BMGC_DS20155,BMG_DS078003,,,Biliary Atresia,,,,,,,D001656,,,,
+BMGC_DS20156,BMG_DS078005,,,Biliary Tract Neoplasms,,,,,,,D001661,,,,
+BMGC_DS20157,BMG_DS078007,,,Birth Weight,,,,,,,D001724,,,,
+BMGC_DS20158,BMG_DS078010,,,Urinary Bladder Calculi,,,,,,,D001744,,,,
+BMGC_DS20159,BMG_DS078012,,,Urinary Bladder Neck Obstruction,,,,,,,D001748,,,,
+BMGC_DS20160,BMG_DS078013,,,Urinary Bladder Neoplasms,,,,,,,D001749,,,,
+BMGC_DS20161,BMG_DS078014,,,Blast Crisis,,,,,,,D001752,,,,
+BMGC_DS20162,BMG_DS078016,,,Blister,,,,,,,D001768,,,,
+BMGC_DS20163,BMG_DS078019,,,Body Weight,,,,,,,D001835,,,,
+BMGC_DS20164,BMG_DS078020,,,Body Weight Changes,,,,,,,D001836,,,,
+BMGC_DS20165,BMG_DS078021,,,Bone Neoplasms,,,,,,,D001859,,,,
+BMGC_DS20166,BMG_DS078022,,,Bone Resorption,,,,DOID:0080011,bone resorption disease,,D001862,,,,
+BMGC_DS20167,BMG_DS078023,,,Bowen's Disease,,,,,,,D001913,,,,
+BMGC_DS20168,BMG_DS078024,,,Bradycardia,,,,,,,D001919,,,,
+BMGC_DS20169,BMG_DS078026,,,Brain Death,,,,,,,D001926,,,,
+BMGC_DS20170,BMG_DS078027,,,Brain Edema,,,,,,,D001929,,,,
+BMGC_DS20171,BMG_DS078028,,,Brain Injuries,,,,,,,D001930,,MONDO:0043510,brain injury,
+BMGC_DS20172,BMG_DS078029,,,Brain Neoplasms,,,,,,,D001932,,,,
+BMGC_DS20173,BMG_DS078031,,,Breast Neoplasms,,,,,,,D001943,,,,
+BMGC_DS20174,BMG_DS078035,,,Bronchial Neoplasms,,,,,,,D001984,,,,
+BMGC_DS20175,BMG_DS078039,,,Bruxism,,,,,,,D002012,,,,
+BMGC_DS20176,BMG_DS078040,,,Bulimia,,,,,,,D002032,,,,
+BMGC_DS20177,BMG_DS078041,,,Burkitt Lymphoma,,,,,,,D002051,,,,
+BMGC_DS20178,BMG_DS078043,,,Burns,,,,,,,D002056,,MONDO:0043519,burn,
+BMGC_DS20179,BMG_DS078044,,,"Burns, Chemical",,,,,,,D002057,,,,
+BMGC_DS20180,BMG_DS078047,,,Cachexia,,,,,,,D002100,,,,
+BMGC_DS20181,BMG_DS078049,,,Cadmium Poisoning,,,,,,,D002105,,MONDO:0043523,cadmium poisoning,
+BMGC_DS20182,BMG_DS078050,,,Calcinosis,,,,,,,D002114,,,,
+BMGC_DS20183,BMG_DS078051,,,Calculi,,,,,,,D002137,,,,
+BMGC_DS20184,BMG_DS078054,,,"Candidiasis, Cutaneous",,,,DOID:0080161,cutaneous candidiasis,,D002179,,,,
+BMGC_DS20185,BMG_DS078055,,,"Candidiasis, Oral",,,,,,,D002180,,,,
+BMGC_DS20186,BMG_DS078056,,,Carbon Monoxide Poisoning,,,,,,,D002249,,,,
+BMGC_DS20187,BMG_DS078057,,,Carbon Tetrachloride Poisoning,,,,,,,D002252,,,,
+BMGC_DS20188,BMG_DS078059,,,Carcinoid Tumor,,,,,,,D002276,,,,
+BMGC_DS20189,BMG_DS078060,,,Carcinoma,,,,,,,D002277,,,,
+BMGC_DS20190,BMG_DS078061,,,Carcinoma in Situ,,,,,,,D002278,,,,
+BMGC_DS20191,BMG_DS078062,,,"Carcinoma 256, Walker",,,,,,,D002279,,,,
+BMGC_DS20192,BMG_DS078063,,,"Carcinoma, Basal Cell",,,,,,,D002280,,,,
+BMGC_DS20193,BMG_DS078065,,,"Adenocarcinoma, Bronchiolo-Alveolar",,,,,,,D002282,,,,
+BMGC_DS20194,BMG_DS078066,,,"Carcinoma, Bronchogenic",,,,,,,D002283,,,,
+BMGC_DS20195,BMG_DS078068,,,"Carcinoma, Intraductal, Noninfiltrating",,,,,,,D002285,,,,
+BMGC_DS20196,BMG_DS078069,,,"Carcinoma, Ehrlich Tumor",,,,,,,D002286,,,,
+BMGC_DS20197,BMG_DS078071,,,"Adenocarcinoma, Mucinous",,,,,,,D002288,,,,
+BMGC_DS20198,BMG_DS078072,,,"Carcinoma, Non-Small-Cell Lung",,,,,,,D002289,,,,
+BMGC_DS20199,BMG_DS078073,,,"Carcinoma, Papillary",,,,,,,D002291,,,,
+BMGC_DS20200,BMG_DS078074,,,"Carcinoma, Renal Cell",,,,,,,D002292,,,,
+BMGC_DS20201,BMG_DS078076,,,"Carcinoma, Squamous Cell",,,,,,,D002294,,,,
+BMGC_DS20202,BMG_DS078077,,,"Carcinoma, Transitional Cell",,,,,,,D002295,,,,
+BMGC_DS20203,BMG_DS078078,,,Carcinosarcoma,,,,,,,D002296,,,,
+BMGC_DS20204,BMG_DS078079,,,"Cardiac Output, Low",,,,,,,D002303,,,,
+BMGC_DS20205,BMG_DS078080,,,"Cardiomyopathy, Restrictive",,,,,,,D002313,,,,
+BMGC_DS20206,BMG_DS078082,,,Catalepsy,,,,,,,D002375,,,,
+BMGC_DS20207,BMG_DS078083,,,Cecal Neoplasms,,,,,,,D002430,,,,
+BMGC_DS20208,BMG_DS078084,,,"Cell Transformation, Neoplastic",,,,,,,D002471,,,,
+BMGC_DS20209,BMG_DS078087,,,Central Nervous System Diseases,,,,,,,D002493,,,,
+BMGC_DS20210,BMG_DS078089,,,"Hypoxia, Brain",,,,,,,D002534,,,,
+BMGC_DS20211,BMG_DS078090,,,Intracranial Arteriovenous Malformations,,,,,,,D002538,,,,
+BMGC_DS20212,BMG_DS078091,,,Cerebral Hemorrhage,,,,,,,D002543,,,,
+BMGC_DS20213,BMG_DS078093,,,Uterine Cervical Dysplasia,,,,,,,D002578,,,,
+BMGC_DS20214,BMG_DS078095,,,Uterine Cervical Neoplasms,,,,,,,D002583,,,,
+BMGC_DS20215,BMG_DS078098,,,,,,,,,,D002640;D006966,,MONDO:0024305,acquired hyperprolactinemia,
+BMGC_DS20216,BMG_DS078100,,,,,,,,,,D002658,,MONDO:0005287,developmental disability,
+BMGC_DS20217,BMG_DS078102,,,Choanal Atresia,,,,,,,D002754,,,,
+BMGC_DS20218,BMG_DS078103,,,"Adenoma, Bile Duct",,,,,,,D002759,,,,
+BMGC_DS20219,BMG_DS078104,,,Chondroblastoma,,,,,,,D002804,,,,
+BMGC_DS20220,BMG_DS078105,,,Chondroma,,,,,,,D002812,,,,
+BMGC_DS20221,BMG_DS078106,,,Chondrosarcoma,,,,,,,D002813,,,,
+BMGC_DS20222,BMG_DS078107,,,Chordoma,,,,,,,D002817,,,,
+BMGC_DS20223,BMG_DS078112,,,Choroid Hemorrhage,,,,,,,D002832,,,,
+BMGC_DS20224,BMG_DS078113,,,Chromosome Aberrations,,,,,,,D002869,,,,
+BMGC_DS20225,BMG_DS078114,,,Chromosome Deletion,,,,,,,D002872,,,,
+BMGC_DS20226,BMG_DS078115,,,Chromosome Fragility,,,,,,,D002873,,,,
+BMGC_DS20227,BMG_DS078117,,,Cleft Lip,,,,,,,D002971,,,,
+BMGC_DS20228,BMG_DS078118,,,Cleft Palate,,,,,,,D002972,,,,
+BMGC_DS20229,BMG_DS078119,,,Clubfoot,,,,,,,D003025,,,,
+BMGC_DS20230,BMG_DS078124,,,Coloboma,,,,,,,D003103,,,,
+BMGC_DS20231,BMG_DS078125,,,Colonic Neoplasms,,,,,,,D003110,,,,
+BMGC_DS20232,BMG_DS078126,,,Colonic Polyps,,,,,,,D003111,,,,
+BMGC_DS20233,BMG_DS078128,,,Communication Disorders,,,,,,,D003147,,,,
+BMGC_DS20234,BMG_DS078129,,,Compartment Syndromes,,,,,,,D003161,,,,
+BMGC_DS20235,BMG_DS078130,,,Confusion,,,,,,,D003221,,,,
+BMGC_DS20236,BMG_DS078134,,,Consciousness Disorders,,,,,,,D003244,,,,
+BMGC_DS20237,BMG_DS078135,,,Constipation,,,,,,,D003248,,,,
+BMGC_DS20238,BMG_DS078136,,,"Constriction, Pathologic",,,,,,,D003251,,,,
+BMGC_DS20239,BMG_DS078137,,,Contracture,,,,,,,D003286,,MONDO:0005307,obsolete contracture,
+BMGC_DS20240,BMG_DS078141,,,Corneal Opacity,,,,,,,D003318,,,,
+BMGC_DS20241,BMG_DS078142,,,Coronary Disease,,,,,,,D003327,,,,
+BMGC_DS20242,BMG_DS078143,,,Coronary Vessel Anomalies,,,,,,,D003330,,,,
+BMGC_DS20243,BMG_DS078144,,,Cough,,,,,,,D003371,,,,
+BMGC_DS20244,BMG_DS078147,,,Craniopharyngioma,,,,,,,D003397,,,,
+BMGC_DS20245,BMG_DS078148,,,Crigler-Najjar Syndrome,,,,,,,D003414,,,,
+BMGC_DS20246,BMG_DS078151,,,Cryptorchidism,,,,,,,D003456,,,,
+BMGC_DS20247,BMG_DS078152,,,Cyanosis,,,,,,,D003490,,,,
+BMGC_DS20248,BMG_DS078153,,,"Carcinoma, Adenoid Cystic",,,,DOID:0080202,adenoid cystic carcinoma,,D003528,,,,
+BMGC_DS20249,BMG_DS078155,,,Cystadenoma,,,,,,,D003537,,,,
+BMGC_DS20250,BMG_DS078156,,,Phyllodes Tumor,,,,,,,D003557,,,,
+BMGC_DS20251,BMG_DS078157,,,Cysts,,,,,,,D003560,,,,
+BMGC_DS20252,BMG_DS078158,,,"Hearing Loss, Sudden",,,,,,,D003639,,,,
+BMGC_DS20253,BMG_DS078159,,,Death,,,,,,,D003643,,,,
+BMGC_DS20254,BMG_DS078160,,,"Death, Sudden",,,,,,,D003645,,,,
+BMGC_DS20255,BMG_DS078162,,,Pressure Ulcer,,,,,,,D003668,,,,
+BMGC_DS20256,BMG_DS078163,,,Delirium,,,,,,,D003693,,,,
+BMGC_DS20257,BMG_DS078164,,,Dementia,,,,,,,D003704,,,,
+BMGC_DS20258,BMG_DS078171,,,"Dermatitis, Exfoliative",,,,,,,D003873,,,,
+BMGC_DS20259,BMG_DS078173,,,Dextrocardia,,,,,,,D003914,,,,
+BMGC_DS20260,BMG_DS078174,,,"Diabetes Mellitus, Experimental",,,,,,,D003921,,,,
+BMGC_DS20261,BMG_DS078177,,,Diarrhea,,,,,,,D003967,,,,
+BMGC_DS20262,BMG_DS078178,,,"Diarrhea, Infantile",,,,,,,D003968,,,,
+BMGC_DS20263,BMG_DS078179,,,Vipoma,,,,,,,D003969,,,,
+BMGC_DS20264,BMG_DS078181,,,Digestive System Abnormalities,,,,,,,D004065,,,,
+BMGC_DS20265,BMG_DS078182,,,Digestive System Neoplasms,,,,,,,D004067,,,,
+BMGC_DS20266,BMG_DS078183,,,"Dilatation, Pathologic",,,,,,,D004108,,,,
+BMGC_DS20267,BMG_DS078185,,,"Disease Models, Animal",,,,,,,D004195,,,,
+BMGC_DS20268,BMG_DS078186,,,Disease Susceptibility,,,,,,,D004198,,,,
+BMGC_DS20269,BMG_DS078189,,,Dizziness,,,,,,,D004244,,,,
+BMGC_DS20270,BMG_DS078191,,,Drug Hypersensitivity,,,,,,,D004342,,,,
+BMGC_DS20271,BMG_DS078192,,,"Ductus Arteriosus, Patent",,,,,,,D004374,,,,
+BMGC_DS20272,BMG_DS078194,,,"Dwarfism, Pituitary",,,,,,,D004393,,,,
+BMGC_DS20273,BMG_DS078195,,,Dysarthria,,,,,,,D004401,,,,
+BMGC_DS20274,BMG_DS078197,,,Dysgeusia,,,,,,,D004408,,,,
+BMGC_DS20275,BMG_DS078198,,,Dyslexia,,,,,,,D004410,,,,
+BMGC_DS20276,BMG_DS078201,,,Dyspepsia,,,,,,,D004415,,,,
+BMGC_DS20277,BMG_DS078203,,,Dyspnea,,,,,,,D004417,,,,
+BMGC_DS20278,BMG_DS078204,,,Dystocia,,,,,,,D004420,,,,
+BMGC_DS20279,BMG_DS078205,,,Dystonia,,,,,,,D004421,,,,
+BMGC_DS20280,BMG_DS078207,,,Ear Neoplasms,,,,,,,D004428,,MONDO:0004532,auditory system cancer,
+BMGC_DS20281,BMG_DS078209,,,Ebstein Anomaly,,,,,,,D004437,,,,
+BMGC_DS20282,BMG_DS078212,,,Ectopia Lentis,,,,,,,D004479,,,,
+BMGC_DS20283,BMG_DS078213,,,Ectromelia,,,,,,,D004480,,,,
+BMGC_DS20284,BMG_DS078214,,,Edema,,,,,,,D004487,,,,
+BMGC_DS20285,BMG_DS078215,,,"Edema, Cardiac",,,,,,,D004489,,,,
+BMGC_DS20286,BMG_DS078217,,,Emaciation,,,,,,,D004614,,,,
+BMGC_DS20287,BMG_DS078218,,,Embolism,,,,,,,D004617,,,,
+BMGC_DS20288,BMG_DS078222,,,Emphysema,,,,,,,D004646,,,,
+BMGC_DS20289,BMG_DS078224,,,Encephalocele,,,,,,,D004677,,,,
+BMGC_DS20290,BMG_DS078227,,,Endocardial Cushion Defects,,,,,,,D004694,,,,
+BMGC_DS20291,BMG_DS078229,,,Endomyocardial Fibrosis,,,,,,,D004719,,,,
+BMGC_DS20292,BMG_DS078231,,,Ependymoma,,,,,,,D004806,,,,
+BMGC_DS20293,BMG_DS078233,,,Epidermodysplasia Verruciformis,,,,,,,D004819,,,,
+BMGC_DS20294,BMG_DS078234,,,Epidermolysis Bullosa,,,,,,,D004820,,,,
+BMGC_DS20295,BMG_DS078236,,,Epistaxis,,,,,,,D004844,,,,
+BMGC_DS20296,BMG_DS078242,,,"Leukemia, Erythroblastic, Acute",,,,,,,D004915,,,,
+BMGC_DS20297,BMG_DS078243,,,Esophageal Atresia,,,,,,,D004933,,,,
+BMGC_DS20298,BMG_DS078247,,,Esophageal Neoplasms,,,,,,,D004938,,,,
+BMGC_DS20299,BMG_DS078249,,,Exanthema,,,,,,,D005076,,,,
+BMGC_DS20300,BMG_DS078250,,,"Exostoses, Multiple Hereditary",,,,,,,D005097,,,,
+BMGC_DS20301,BMG_DS078251,,,Extravasation of Diagnostic and Therapeutic Materials,,,,,,,D005119,,,,
+BMGC_DS20302,BMG_DS078252,,,Eye Abnormalities,,,,,,,D005124,,,,
+BMGC_DS20303,BMG_DS078253,,,Eye Burns,,,,,,,D005126,,,,
+BMGC_DS20304,BMG_DS078254,,,Eye Diseases,,,,DOID:0070356,visual impairment and progressive phthisis bulbi,,D005128,,,,
+BMGC_DS20305,BMG_DS078256,,,Eye Hemorrhage,,,,,,,D005130,,,,
+BMGC_DS20306,BMG_DS078257,,,Eye Injuries,,,,,,,D005131,,,,
+BMGC_DS20307,BMG_DS078258,,,Eye Manifestations,,,,,,,D005132,,,,
+BMGC_DS20308,BMG_DS078259,,,Eye Neoplasms,,,,,,,D005134,,,,
+BMGC_DS20309,BMG_DS078261,,,Facial Asymmetry,,,,,,,D005146,,,,
+BMGC_DS20310,BMG_DS078262,,,Facial Injuries,,,,,,,D005151,,,,
+BMGC_DS20311,BMG_DS078264,,,Facial Pain,,,,,,,D005157,,,,
+BMGC_DS20312,BMG_DS078265,,,Factor V Deficiency,,,,,,,D005166,,,,
+BMGC_DS20313,BMG_DS078266,,,Factor XI Deficiency,,,,,,,D005173,,,,
+BMGC_DS20314,BMG_DS078267,,,Factor XIII Deficiency,,,,,,,D005177,,,,
+BMGC_DS20315,BMG_DS078269,,,Fasciculation,,,,,,,D005207,,,,
+BMGC_DS20316,BMG_DS078271,,,Fatigue,,,,,,,D005221,,,,
+BMGC_DS20317,BMG_DS078274,,,Feminization,,,,,,,D005262,,,,
+BMGC_DS20318,BMG_DS078275,,,Femoral Fractures,,,,,,,D005264,,,,
+BMGC_DS20319,BMG_DS078278,,,Fetal Death,,,,,,,D005313,,,,
+BMGC_DS20320,BMG_DS078279,,,Fetal Distress,,,,,,,D005316,,,,
+BMGC_DS20321,BMG_DS078280,,,Fetal Growth Retardation,,,,,,,D005317,,,,
+BMGC_DS20322,BMG_DS078281,,,Fetal Macrosomia,,,,,,,D005320,,,,
+BMGC_DS20323,BMG_DS078284,,,Fever,,,,,,,D005334,,,,
+BMGC_DS20324,BMG_DS078286,,,Fibroma,,,,DOID:0050871,fibroma,,D005350,,,,
+BMGC_DS20325,BMG_DS078288,,,Fibrosarcoma,,,,,,,D005354,,,,
+BMGC_DS20326,BMG_DS078289,,,Finger Injuries,,,,,,,D005383,,,,
+BMGC_DS20327,BMG_DS078290,,,Fistula,,,,,,,D005402,,,,
+BMGC_DS20328,BMG_DS078292,,,Flatfoot,,,,,,,D005413,,,,
+BMGC_DS20329,BMG_DS078294,,,Fluoride Poisoning,,,,,,,D005458,,,,
+BMGC_DS20330,BMG_DS078295,,,Flushing,,,,,,,D005483,,,,
+BMGC_DS20331,BMG_DS078297,,,Follicular Cyst,,,,,,,D005497,,,,
+BMGC_DS20332,BMG_DS078298,,,Foodborne Diseases,,,,,,,D005517,,,,
+BMGC_DS20333,BMG_DS078301,,,"Foot Deformities, Congenital",,,,,,,D005532,,,,
+BMGC_DS20334,BMG_DS078305,,,Foreign-Body Reaction,,,,,,,D005549,,,,
+BMGC_DS20335,BMG_DS078307,,,"Fractures, Closed",,,,,,,D005596,,,,
+BMGC_DS20336,BMG_DS078312,,,Fructose Intolerance,,,,,,,D005633,,,,
+BMGC_DS20337,BMG_DS078316,,,Gallbladder Neoplasms,,,,,,,D005706,,,,
+BMGC_DS20338,BMG_DS078318,,,Gas Poisoning,,,,,,,D005739,,,,
+BMGC_DS20339,BMG_DS078319,,,Gastric Fistula,,,,,,,D005747,,,,
+BMGC_DS20340,BMG_DS078320,,,Gastroesophageal Reflux,,,,,,,D005764,,,,
+BMGC_DS20341,BMG_DS078321,,,Gastrointestinal Neoplasms,,,,,,,D005770,,,,
+BMGC_DS20342,BMG_DS078322,,,"Genital Neoplasms, Female",,,,,,,D005833,,,,
+BMGC_DS20343,BMG_DS078325,,,Castleman Disease,,,,,,,D005871,,,,
+BMGC_DS20344,BMG_DS078326,,,Tourette Syndrome,,,,,,,D005879,,,,
+BMGC_DS20345,BMG_DS078327,,,Gingival Hemorrhage,,,,,,,D005884,,,,
+BMGC_DS20346,BMG_DS078328,,,Gingival Hyperplasia,,,,,,,D005885,,,,
+BMGC_DS20347,BMG_DS078331,,,Gingival Recession,,,,,,,D005889,,,,
+BMGC_DS20348,BMG_DS078332,,,Glioblastoma,,,,,,,D005909,,,,
+BMGC_DS20349,BMG_DS078333,,,Glioma,,,,,,,D005910,,,,
+BMGC_DS20350,BMG_DS078334,,,Gliosis,,,,,,,D005911,,,,
+BMGC_DS20351,BMG_DS078337,,,Glossalgia,,,,,,,D005926,,,,
+BMGC_DS20352,BMG_DS078338,,,Glucagonoma,,,,,,,D005935,,,,
+BMGC_DS20353,BMG_DS078339,,,Glucosephosphate Dehydrogenase Deficiency,,,,,,,D005955,,,,
+BMGC_DS20354,BMG_DS078340,,,Glycosuria,,,,,,,D006029,,,,
+BMGC_DS20355,BMG_DS078341,,,"Glycosuria, Renal",,,,,,,D006030,,,,
+BMGC_DS20356,BMG_DS078343,,,Gonadal Dysgenesis,,,,,,,D006059,,,,
+BMGC_DS20357,BMG_DS078344,,,"Graft Occlusion, Vascular",,,,,,,D006083,,,,
+BMGC_DS20358,BMG_DS078345,,,Granuloma,,,,,,,D006099,,,,
+BMGC_DS20359,BMG_DS078346,,,"Granuloma, Plasma Cell",,,,,,,D006104,,,,
+BMGC_DS20360,BMG_DS078347,,,Granulosa Cell Tumor,,,,,,,D006106,,,,
+BMGC_DS20361,BMG_DS078348,,,Growth Disorders,,,,,,,D006130,,,,
+BMGC_DS20362,BMG_DS078349,,,Halitosis,,,,,,,D006209,,,,
+BMGC_DS20363,BMG_DS078350,,,Hallucinations,,,,,,,D006212,,,,
+BMGC_DS20364,BMG_DS078352,,,Hamartoma,,,,,,,D006222,,,,
+BMGC_DS20365,BMG_DS078355,,,"Hand Deformities, Congenital",,,,,,,D006228,,,,
+BMGC_DS20366,BMG_DS078357,,,"Rhinitis, Allergic, Seasonal",,,,,,,D006255,,,,
+BMGC_DS20367,BMG_DS078358,,,Head and Neck Neoplasms,,,,,,,D006258,,,,
+BMGC_DS20368,BMG_DS078359,,,Craniocerebral Trauma,,,,,,,D006259,,,,
+BMGC_DS20369,BMG_DS078360,,,Headache,,,,,,,D006261,,,,
+BMGC_DS20370,BMG_DS078361,,,"Hearing Loss, Conductive",,,,,,,D006314,,,,
+BMGC_DS20371,BMG_DS078363,,,"Hearing Loss, Noise-Induced",,,,,,,D006317,,,,
+BMGC_DS20372,BMG_DS078364,,,"Hearing Loss, Sensorineural",,,,,,,D006319,,,,
+BMGC_DS20373,BMG_DS078365,,,"Heart Defects, Congenital",,,,,,,D006330,,,,
+BMGC_DS20374,BMG_DS078366,,,Cardiomegaly,,,,,,,D006332,,,,
+BMGC_DS20375,BMG_DS078367,,,Heart Injuries,,,,,,,D006335,,,,
+BMGC_DS20376,BMG_DS078369,,,Heart Septal Defects,,,,,,,D006343,,,,
+BMGC_DS20377,BMG_DS078370,,,"Heart Septal Defects, Atrial",,,,,,,D006344,,,,
+BMGC_DS20378,BMG_DS078371,,,"Heart Septal Defects, Ventricular",,,,,,,D006345,,,,
+BMGC_DS20379,BMG_DS078372,,,Heart Valve Diseases,,,,,,,D006349,,,,
+BMGC_DS20380,BMG_DS078373,,,Heartburn,,,,,,,D006356,,,,
+BMGC_DS20381,BMG_DS078376,,,Hemangioendothelioma,,,,,,,D006390,,,,
+BMGC_DS20382,BMG_DS078377,,,Hemangioma,,,,,,,D006391,,,,
+BMGC_DS20383,BMG_DS078379,,,Hemangiopericytoma,,,,,,,D006393,,,,
+BMGC_DS20384,BMG_DS078380,,,Hemangiosarcoma,,,,,,,D006394,,,,
+BMGC_DS20385,BMG_DS078382,,,Hematemesis,,,,,,,D006396,,,,
+BMGC_DS20386,BMG_DS078384,,,Hematoma,,,,,,,D006406,,,,
+BMGC_DS20387,BMG_DS078385,,,"Hematoma, Epidural, Cranial",,,,,,,D006407,,,,
+BMGC_DS20388,BMG_DS078386,,,"Hematoma, Subdural",,,,,,,D006408,,,,
+BMGC_DS20389,BMG_DS078389,,,Hemoglobinuria,,,,,,,D006456,,,,
+BMGC_DS20390,BMG_DS078390,,,Hemolysis,,,,,,,D006461,,,,
+BMGC_DS20391,BMG_DS078391,,,Hemoperitoneum,,,,,,,D006465,,,,
+BMGC_DS20392,BMG_DS078393,,,Hemorrhage,,,,,,,D006470,,,,
+BMGC_DS20393,BMG_DS078395,,,Postpartum Hemorrhage,,,,,,,D006473,,,,
+BMGC_DS20394,BMG_DS078396,,,Hemothorax,,,,,,,D006491,,,,
+BMGC_DS20395,BMG_DS078397,,,"Carcinoma, Hepatocellular",,,,,,,D006528,,,,
+BMGC_DS20396,BMG_DS078398,,,Hepatomegaly,,,,,,,D006529,,,,
+BMGC_DS20397,BMG_DS078400,,,"Hernia, Diaphragmatic",,,,,,,D006548,,,,
+BMGC_DS20398,BMG_DS078404,,,"Hernia, Umbilical",,,,,,,D006554,,MONDO:0000747,obsolete umbilical hernia,
+BMGC_DS20399,BMG_DS078406,,,Heroin Dependence,,,,,,,D006556,,,,
+BMGC_DS20400,BMG_DS078407,,,Herpes Simplex,,,,,,,D006561,,,,
+BMGC_DS20401,BMG_DS078409,,,Hiccup,,,,,,,D006606,,,,
+BMGC_DS20402,BMG_DS078414,,,Hip Fractures,,,,,,,D006620,,MONDO:0005327,hip fracture,
+BMGC_DS20403,BMG_DS078415,,,von Hippel-Lindau Disease,,,,,,,D006623,,,,
+BMGC_DS20404,BMG_DS078416,,,HIV Seropositivity,,,,,,,D006679,,,,
+BMGC_DS20405,BMG_DS078418,,,Hodgkin Disease,,,,,,,D006689,,MONDO:0004952,Hodgkins lymphoma,
+BMGC_DS20406,BMG_DS078420,,,Hydatidiform Mole,,,,,,,D006828,,,,
+BMGC_DS20407,BMG_DS078421,,,Polyhydramnios,,,,,,,D006831,,,,
+BMGC_DS20408,BMG_DS078422,,,Hydranencephaly,,,,,,,D006832,,,,
+BMGC_DS20409,BMG_DS078424,,,Testicular Hydrocele,,,,,,,D006848,,,,
+BMGC_DS20410,BMG_DS078427,,,Hyperalgesia,,,,,,,D006930,,,,
+BMGC_DS20411,BMG_DS078428,,,Hypercapnia,,,,,,,D006935,,,,
+BMGC_DS20412,BMG_DS078430,,,Hyperesthesia,,,,,,,D006941,,,,
+BMGC_DS20413,BMG_DS078431,,,Hyperhidrosis,,,,,,,D006945,,,,
+BMGC_DS20414,BMG_DS078432,,,Hyperkalemia,,,,,,,D006947,,,,
+BMGC_DS20415,BMG_DS078433,,,Hyperphagia,,,,,,,D006963,,,,
+BMGC_DS20416,BMG_DS078434,,,Hyperplasia,,,,,,,D006965,,,,
+BMGC_DS20417,BMG_DS078435,,,Hypersensitivity,,,,,,,D006967,,,,
+BMGC_DS20418,BMG_DS078436,,,"Hypersensitivity, Delayed",,,,,,,D006968,,,,
+BMGC_DS20419,BMG_DS078437,,,"Hypersensitivity, Immediate",,,,,,,D006969,,,,
+BMGC_DS20420,BMG_DS078438,,,Hypertelorism,,,,,,,D006972,145400,MONDO:0007778,obsolete hypertelorism,
+BMGC_DS20421,BMG_DS078439,,,Hypertension,,,,,,,D006973,,,,
+BMGC_DS20422,BMG_DS078440,,,"Hypertension, Pulmonary",,,,,,,D006976,,,,
+BMGC_DS20423,BMG_DS078441,,,"Hypertension, Renal",,,,,,,D006977,,,,
+BMGC_DS20424,BMG_DS078442,,,Hypertrophy,,,,,,,D006984,,,,
+BMGC_DS20425,BMG_DS078443,,,Hyperventilation,,,,,,,D006985,,,,
+BMGC_DS20426,BMG_DS078444,,,Hypesthesia,,,,,,,D006987,,,,
+BMGC_DS20427,BMG_DS078445,,,Hyphema,,,,,,,D006988,,,,
+BMGC_DS20428,BMG_DS078446,,,Hypokalemia,,,,,,,D007008,,,,
+BMGC_DS20429,BMG_DS078448,,,Hypospadias,,,,,,,D007021,,,,
+BMGC_DS20430,BMG_DS078449,,,Hypotension,,,,,,,D007022,,,,
+BMGC_DS20431,BMG_DS078451,,,Hypothermia,,,,,,,D007035,,,,
+BMGC_DS20432,BMG_DS078452,,,Hypoventilation,,,,,,,D007040,,,,
+BMGC_DS20433,BMG_DS078456,,,Immunoblastic Lymphadenopathy,,,,,,,D007119,,,,
+BMGC_DS20434,BMG_DS078457,,,Immunoproliferative Disorders,,,,,,,D007160,,,,
+BMGC_DS20435,BMG_DS078459,,,Erectile Dysfunction,,,,,,,D007172,,,,
+BMGC_DS20436,BMG_DS078460,,,Incontinentia Pigmenti,,,,,,,D007184,,,,
+BMGC_DS20437,BMG_DS078462,,,"Infant, Newborn, Diseases",,,,,,,D007232,,,,
+BMGC_DS20438,BMG_DS078463,,,Infarction,,,,,,,D007238,,,,
+BMGC_DS20439,BMG_DS078464,,,Infections,,,,,,,D007239,,,,
+BMGC_DS20440,BMG_DS078465,,,Infertility,,,,,,,D007246,,,,
+BMGC_DS20441,BMG_DS078466,,,"Infertility, Male",,,,,,,D007248,,,,
+BMGC_DS20442,BMG_DS078467,,,Inflammation,,,,,,,D007249,,,,
+BMGC_DS20443,BMG_DS078468,,,Insect Bites and Stings,,,,,,,D007299,,,,
+BMGC_DS20444,BMG_DS078469,,,Insulin Resistance,,,,,,,D007333,,,,
+BMGC_DS20445,BMG_DS078470,,,Insulinoma,,,,,,,D007340,,,,
+BMGC_DS20446,BMG_DS078471,,,Intestinal Neoplasms,,,,,,,D007414,,,,
+BMGC_DS20447,BMG_DS078472,,,Intestinal Polyps,,,,,,,D007417,,,,
+BMGC_DS20448,BMG_DS078473,,,Intraoperative Complications,,,,,,,D007431,,,,
+BMGC_DS20449,BMG_DS078475,,,Ischemia,,,,,,,D007511,,,,
+BMGC_DS20450,BMG_DS078476,,,"Adenoma, Islet Cell",,,,,,,D007516,,,,
+BMGC_DS20451,BMG_DS078477,,,Jaw Abnormalities,,,,,,,D007569,,,,
+BMGC_DS20452,BMG_DS078482,,,Joint Instability,,,,,,,D007593,,,,
+BMGC_DS20453,BMG_DS078484,,,Kearns-Sayre Syndrome,,,,,,,D007625,,,,
+BMGC_DS20454,BMG_DS078485,,,Keloid,,,,,,,D007627,,,,
+BMGC_DS20455,BMG_DS078486,,,,,,,DOID:0080158,herpes simplex virus keratitis,,D007635,,,,
+BMGC_DS20456,BMG_DS078487,,,Keratoacanthoma,,,,,,,D007636,,,,
+BMGC_DS20457,BMG_DS078488,,,Kidney Calculi,,,,,,,D007669,,,,
+BMGC_DS20458,BMG_DS078489,,,Kidney Neoplasms,,,,,,,D007680,,,,
+BMGC_DS20459,BMG_DS078493,,,Kyphosis,,,,,,,D007738,,,,
+BMGC_DS20460,BMG_DS078495,,,"Obstetric Labor, Premature",,,,,,,D007752,,,,
+BMGC_DS20461,BMG_DS078496,,,Labyrinth Diseases,,,,,,,D007759,,,,
+BMGC_DS20462,BMG_DS078497,,,Lacrimal Duct Obstruction,,,,,,,D007767,,,,
+BMGC_DS20463,BMG_DS078498,,,"Lameness, Animal",,,,,,,D007794,,MONDO:0024953,"lameness, non-human animal",
+BMGC_DS20464,BMG_DS078499,,,Language Disorders,,,,,,,D007806,,,,
+BMGC_DS20465,BMG_DS078500,,,Laryngeal Edema,,,,,,,D007819,,,,
+BMGC_DS20466,BMG_DS078501,,,Laryngeal Neoplasms,,,,,,,D007822,,,,
+BMGC_DS20467,BMG_DS078503,,,Lead Poisoning,,,,,,,D007855,,MONDO:0018019,lead poisoning,
+BMGC_DS20468,BMG_DS078504,,,Learning Disabilities,,,,,,,D007859,,,,
+BMGC_DS20469,BMG_DS078507,,,Legg-Calve-Perthes Disease,,,,,,,D007873,,,,
+BMGC_DS20470,BMG_DS078508,,,Leiomyoma,,,,,,,D007889,,,,
+BMGC_DS20471,BMG_DS078509,,,Leiomyosarcoma,,,,,,,D007890,,,,
+BMGC_DS20472,BMG_DS078510,,,"Leishmaniasis, Mucocutaneous",,,,,,,D007897,,,,
+BMGC_DS20473,BMG_DS078511,,,Leukemia,,,,,,,D007938,,,,
+BMGC_DS20474,BMG_DS078512,,,Leukemia L1210,,,,,,,D007939,,,,
+BMGC_DS20475,BMG_DS078515,,,"Leukemia, Experimental",,,,,,,D007942,,,,
+BMGC_DS20476,BMG_DS078516,,,"Leukemia, Hairy Cell",,,,,,,D007943,,,,
+BMGC_DS20477,BMG_DS078517,,,"Leukemia, Lymphoid",,,,,,,D007945,,,,
+BMGC_DS20478,BMG_DS078519,,,"Leukemia, Megakaryoblastic, Acute",,,,,,,D007947,,,,
+BMGC_DS20479,BMG_DS078520,,,"Leukemia, Monocytic, Acute",,,,,,,D007948,,,,
+BMGC_DS20480,BMG_DS078521,,,"Leukemia, Myeloid",,,,,,,D007951,,,,
+BMGC_DS20481,BMG_DS078523,,,"Leukemia, Radiation-Induced",,,,,,,D007953,,,,
+BMGC_DS20482,BMG_DS078525,,,"Leukoplakia, Oral",,,,,,,D007972,,,,
+BMGC_DS20483,BMG_DS078528,,,Leydig Cell Tumor,,,,,,,D007984,,,,
+BMGC_DS20484,BMG_DS078529,,,Linitis Plastica,,,,,,,D008039,,,,
+BMGC_DS20485,BMG_DS078531,,,Lipoma,,,,,,,D008067,,,,
+BMGC_DS20486,BMG_DS078532,,,Liposarcoma,,,,,,,D008080,,,,
+BMGC_DS20487,BMG_DS078533,,,"Liver Cirrhosis, Experimental",,,,,,,D008106,,,,
+BMGC_DS20488,BMG_DS078534,,,Liver Diseases,,,,,,,D008107,,,,
+BMGC_DS20489,BMG_DS078535,,,Liver Neoplasms,,,,,,,D008113,,,,
+BMGC_DS20490,BMG_DS078536,,,"Liver Neoplasms, Experimental",,,,,,,D008114,,,,
+BMGC_DS20491,BMG_DS078538,,,Long QT Syndrome,,,,,,,D008133,,,,
+BMGC_DS20492,BMG_DS078539,,,Lordosis,,,,,,,D008141,,,,
+BMGC_DS20493,BMG_DS078545,,,Lung Diseases,,,,,,,D008171,,,,
+BMGC_DS20494,BMG_DS078546,,,Lung Neoplasms,,,,,,,D008175,,,,
+BMGC_DS20495,BMG_DS078547,,,"Lupus Erythematosus, Discoid",,,,,,,D008179,,,,
+BMGC_DS20496,BMG_DS078551,,,Lymphatic Metastasis,,,,,,,D008207,,,,
+BMGC_DS20497,BMG_DS078552,,,Lymphoma,,,,,,,D008223,,,,
+BMGC_DS20498,BMG_DS078553,,,"Lymphoma, Follicular",,,,DOID:0050873,follicular lymphoma,,D008224,,,,
+BMGC_DS20499,BMG_DS078554,,,"Lymphoma, Non-Hodgkin",,,,,,,D008228,,,,
+BMGC_DS20500,BMG_DS078556,,,Lymphoproliferative Disorders,,,,,,,D008232,,,,
+BMGC_DS20501,BMG_DS078557,,,Waldenstrom Macroglobulinemia,,,,,,,D008258,,MONDO:0005190,obsolete macroglobulinemia,
+BMGC_DS20502,BMG_DS078558,,,Macrostomia,,,,,,,D008265,,,,
+BMGC_DS20503,BMG_DS078559,,,Macular Degeneration,,,,,,,D008268,,,,
+BMGC_DS20504,BMG_DS078562,,,Malignant Hyperthermia,,,,,,,D008305,,,,
+BMGC_DS20505,BMG_DS078563,,,Malocclusion,,,,,,,D008310,,,,
+BMGC_DS20506,BMG_DS078567,,,"Mammary Neoplasms, Experimental",,,,,,,D008325,,,,
+BMGC_DS20507,BMG_DS078570,,,Mandibular Neoplasms,,,,,,,D008339,,,,
+BMGC_DS20508,BMG_DS078572,,,Mastocytosis,,,,,,,D008415,,,,
+BMGC_DS20509,BMG_DS078574,,,Maxillary Neoplasms,,,,,,,D008441,,,,
+BMGC_DS20510,BMG_DS078575,,,Maxillary Sinus Neoplasms,,,,,,,D008444,,,,
+BMGC_DS20511,BMG_DS078578,,,Mediastinal Neoplasms,,,,,,,D008479,,,,
+BMGC_DS20512,BMG_DS078579,,,Medulloblastoma,,,,,,,D008527,,,,
+BMGC_DS20513,BMG_DS078580,,,Megacolon,,,,,,,D008531,,,,
+BMGC_DS20514,BMG_DS078582,,,Melanoma,,,,,,,D008545,,,,
+BMGC_DS20515,BMG_DS078583,,,"Melanoma, Experimental",,,,,,,D008546,,,,
+BMGC_DS20516,BMG_DS078584,,,Melena,,,,,,,D008551,,,,
+BMGC_DS20517,BMG_DS078585,,,Memory Disorders,,,,,,,D008569,,,,
+BMGC_DS20518,BMG_DS078587,,,Meningioma,,,,,,,D008579,,,,
+BMGC_DS20519,BMG_DS078588,,,Meningism,,,,,,,D008580,,,,
+BMGC_DS20520,BMG_DS078590,,,Meningocele,,,,,,,D008588,,,,
+BMGC_DS20521,BMG_DS078591,,,Meningomyelocele,,,,,,,D008591,,,,
+BMGC_DS20522,BMG_DS078592,,,Menorrhagia,,,,,,,D008595,,,,
+BMGC_DS20523,BMG_DS078593,,,Intellectual Disability,,,,,,,D008607,,,,
+BMGC_DS20524,BMG_DS078594,,,Mercury Poisoning,,,,,,,D008630,,MONDO:0018020,mercury poisoning,
+BMGC_DS20525,BMG_DS078599,,,Mesothelioma,,,,,,,D008654,,,,
+BMGC_DS20526,BMG_DS078600,,,Metaplasia,,,,,,,D008679,,,,
+BMGC_DS20527,BMG_DS078601,,,Metrorrhagia,,,,,,,D008796,,,,
+BMGC_DS20528,BMG_DS078602,,,Micrognathism,,,,,,,D008844,,,,
+BMGC_DS20529,BMG_DS078603,,,Microphthalmos,,,,,,,D008850,,,,
+BMGC_DS20530,BMG_DS078606,,,Monoclonal Gammopathy of Undetermined Significance,,,,,,,D008998,,,,
+BMGC_DS20531,BMG_DS078607,,,Monosomy,,,,,,,D009006,,,,
+BMGC_DS20532,BMG_DS078608,,,"Abnormalities, Severe Teratoid",,,,,,,D009008,,,,
+BMGC_DS20533,BMG_DS078610,,,Morphine Dependence,,,,,,,D009021,,,,
+BMGC_DS20534,BMG_DS078611,,,"Fluorosis, Dental",,,,,,,D009050,,,,
+BMGC_DS20535,BMG_DS078612,,,Mouth Abnormalities,,,,,,,D009056,,,,
+BMGC_DS20536,BMG_DS078613,,,Mouth Breathing,,,,,,,D009058,,,,
+BMGC_DS20537,BMG_DS078614,,,Mouth Neoplasms,,,,,,,D009062,,,,
+BMGC_DS20538,BMG_DS078616,,,Mucocele,,,,,,,D009078,,,,
+BMGC_DS20539,BMG_DS078617,,,Multiple Myeloma,,,,,,,D009101,,,,
+BMGC_DS20540,BMG_DS078619,,,Muscle Cramp,,,,,,,D009120,,,,
+BMGC_DS20541,BMG_DS078620,,,Muscle Hypertonia,,,,,,,D009122,,,,
+BMGC_DS20542,BMG_DS078621,,,Muscle Rigidity,,,,,,,D009127,,,,
+BMGC_DS20543,BMG_DS078622,,,Muscle Spasticity,,,,,,,D009128,,,,
+BMGC_DS20544,BMG_DS078623,,,Muscular Atrophy,,,,,,,D009133,,,,
+BMGC_DS20545,BMG_DS078624,,,Musculoskeletal Abnormalities,,,,,,,D009139,,,,
+BMGC_DS20546,BMG_DS078626,,,Mycosis Fungoides,,,,,,,D009182,,,,
+BMGC_DS20547,BMG_DS078627,,,Myelodysplastic Syndromes,,,,,,,D009190,,,,
+BMGC_DS20548,BMG_DS078628,,,Myeloproliferative Disorders,,,,,,,D009196,,,,
+BMGC_DS20549,BMG_DS078630,,,Myoglobinuria,,,,DOID:0080108,myoglobinuria,,D009212,,MONDO:0000866,obsolete hereditary myoglobinuria,
+BMGC_DS20550,BMG_DS078631,,,Myoma,,,,,,,D009214,,,,
+BMGC_DS20551,BMG_DS078633,,,Myotonia,,,,,,,D009222,,,,
+BMGC_DS20552,BMG_DS078637,,,Opioid-Related Disorders,,,,,,,D009293,,,,
+BMGC_DS20553,BMG_DS078638,,,Nasal Polyps,,,,,,,D009298,,,,
+BMGC_DS20554,BMG_DS078639,,,Nasopharyngeal Neoplasms,,,,,,,D009303,,,,
+BMGC_DS20555,BMG_DS078640,,,Nausea,,,,,,,D009325,,,,
+BMGC_DS20556,BMG_DS078641,,,Necrosis,,,,,,,D009336,,,,
+BMGC_DS20557,BMG_DS078643,,,Nematode Infections,,,,,,,D009349,,,,
+BMGC_DS20558,BMG_DS078644,,,"Neoplastic Cells, Circulating",,,,,,,D009360,,,,
+BMGC_DS20559,BMG_DS078645,,,Neoplasm Invasiveness,,,,,,,D009361,,,,
+BMGC_DS20560,BMG_DS078646,,,Neoplasm Metastasis,,,,,,,D009362,,,,
+BMGC_DS20561,BMG_DS078647,,,"Neoplasm Recurrence, Local",,,,,,,D009364,,,,
+BMGC_DS20562,BMG_DS078648,,,"Neoplasm Regression, Spontaneous",,,,,,,D009365,,,,
+BMGC_DS20563,BMG_DS078649,,,Neoplasm Seeding,,,,,,,D009366,,,,
+BMGC_DS20564,BMG_DS078650,,,Neoplasms,,,,,,,D009369,,,,
+BMGC_DS20565,BMG_DS078652,,,Neoplasms by Site,,,,DOID:0050686,organ system cancer,,D009371,,,,
+BMGC_DS20566,BMG_DS078654,,,"Neoplasms, Germ Cell and Embryonal",,,,,,,D009373,,MONDO:0002510,obsolete germ cell and embryonal cancer,
+BMGC_DS20567,BMG_DS078655,,,"Neoplasms, Experimental",,,,,,,D009374,,,,
+BMGC_DS20568,BMG_DS078656,,,"Neoplasms, Glandular and Epithelial",,,,,,,D009375,,,,
+BMGC_DS20569,BMG_DS078657,,,"Neoplasms, Hormone-Dependent",,,,,,,D009376,,,,
+BMGC_DS20570,BMG_DS078658,,,Multiple Endocrine Neoplasia,,,,DOID:3125,multiple endocrine neoplasia,,D009377,,,,
+BMGC_DS20571,BMG_DS078662,,,"Neoplasms, Radiation-Induced",,,,,,,D009381,,,,
+BMGC_DS20572,BMG_DS078665,,,Neoplastic Processes,,,,,,,D009385,,,,
+BMGC_DS20573,BMG_DS078667,,,"Neovascularization, Pathologic",,,,,,,D009389,,,,
+BMGC_DS20574,BMG_DS078668,,,Nerve Degeneration,,,,,,,D009410,,,,
+BMGC_DS20575,BMG_DS078669,,,Nervous System Malformations,,,,,,,D009421,,,,
+BMGC_DS20576,BMG_DS078670,,,Nervous System Diseases,,,,,,,D009422,,,,
+BMGC_DS20577,BMG_DS078672,,,Neurilemmoma,,,,,,,D009442,,,,
+BMGC_DS20578,BMG_DS078673,,,"Neuritis, Autoimmune, Experimental",,,,,,,D009444,,,,
+BMGC_DS20579,BMG_DS078674,,,Neuroblastoma,,,,,,,D009447,,,,
+BMGC_DS20580,BMG_DS078675,,,Neurofibroma,,,,,,,D009455,,,,
+BMGC_DS20581,BMG_DS078676,,,Neurofibromatosis 1,,,,,,,D009456,,,,
+BMGC_DS20582,BMG_DS078677,,,Neurologic Manifestations,,,,,,,D009461,,,,
+BMGC_DS20583,BMG_DS078680,,,Nevus,,,,,,,D009506,,,,
+BMGC_DS20584,BMG_DS078682,,,"Nevus, Pigmented",,,,,,,D009508,,,,
+BMGC_DS20585,BMG_DS078684,,,"Nose Deformities, Acquired",,,,,,,D009667,,,,
+BMGC_DS20586,BMG_DS078685,,,Nose Neoplasms,,,,,,,D009669,,,,
+BMGC_DS20587,BMG_DS078686,,,"Obesity, Morbid",,,,,,,D009767,,,,
+BMGC_DS20588,BMG_DS078689,,,Oligodendroglioma,,,,,,,D009837,,,,
+BMGC_DS20589,BMG_DS078690,,,Oligomenorrhea,,,,,,,D009839,,,,
+BMGC_DS20590,BMG_DS078696,,,Oropharyngeal Neoplasms,,,,,,,D009959,,,,
+BMGC_DS20591,BMG_DS078697,,,"Ossification, Heterotopic",,,,,,,D009999,,,,
+BMGC_DS20592,BMG_DS078698,,,Osteolysis,,,,,,,D010014,,,,
+BMGC_DS20593,BMG_DS078705,,,Ovarian Neoplasms,,,,,,,D010051,,,,
+BMGC_DS20594,BMG_DS078707,,,"Paget Disease, Extramammary",,,,DOID:3450,cutaneous Paget's disease,,D010145,,MONDO:0002655,cutaneous Paget disease,
+BMGC_DS20595,BMG_DS078708,,,Pain,,,,,,,D010146,,,,
+BMGC_DS20596,BMG_DS078709,,,"Pain, Intractable",,,,,,,D010148,,,,
+BMGC_DS20597,BMG_DS078713,,,Exocrine Pancreatic Insufficiency,,,,,,,D010188,,,,
+BMGC_DS20598,BMG_DS078714,,,Pancreatic Neoplasms,,,,,,,D010190,,,,
+BMGC_DS20599,BMG_DS078715,,,Papilloma,,,,,,,D010212,,,,
+BMGC_DS20600,BMG_DS078716,,,Paraganglioma,,,,,,,D010235,,,,
+BMGC_DS20601,BMG_DS078717,,,"Paraganglioma, Extra-Adrenal",,,,,,,D010236,,,,
+BMGC_DS20602,BMG_DS078718,,,Paralysis,,,,,,,D010243,,,,
+BMGC_DS20603,BMG_DS078720,,,Paranasal Sinus Diseases,,,,,,,D010254,,,,
+BMGC_DS20604,BMG_DS078722,,,Paraneoplastic Syndromes,,,,,,,D010257,,,,
+BMGC_DS20605,BMG_DS078723,,,Parathyroid Neoplasms,,,,,,,D010282,,,,
+BMGC_DS20606,BMG_DS078728,,,"Pemphigoid, Bullous",,,,,,,D010391,,,,
+BMGC_DS20607,BMG_DS078729,,,Penile Neoplasms,,,,,,,D010412,,,,
+BMGC_DS20608,BMG_DS078730,,,Peptic Ulcer Hemorrhage,,,,,,,D010438,,MONDO:0004242,active peptic ulcer disease,
+BMGC_DS20609,BMG_DS078731,,,Perceptual Disorders,,,,,,,D010468,,,,
+BMGC_DS20610,BMG_DS078735,,,Peritoneal Neoplasms,,,,,,,D010534,,,,
+BMGC_DS20611,BMG_DS078736,,,Pharyngeal Neoplasms,,,,,,,D010610,,,,
+BMGC_DS20612,BMG_DS078737,,,Phencyclidine Abuse,,,,,,,D010623,,,,
+BMGC_DS20613,BMG_DS078738,,,Pheochromocytoma,,,,DOID:0050771,pheochromocytoma,,D010673,,,,
+BMGC_DS20614,BMG_DS078739,,,Philadelphia Chromosome,,,,,,,D010677,,,,
+BMGC_DS20615,BMG_DS078741,,,Pica,,,,,,,D010842,,,,
+BMGC_DS20616,BMG_DS078742,,,Pierre Robin Syndrome,,,,,,,D010855,,,,
+BMGC_DS20617,BMG_DS078743,,,Pilonidal Sinus,,,,,,,D010864,,,,
+BMGC_DS20618,BMG_DS078745,,,Pituitary Neoplasms,,,,,,,D010911,,,,
+BMGC_DS20619,BMG_DS078746,,,Placenta Accreta,,,,,,,D010921,,,,
+BMGC_DS20620,BMG_DS078747,,,Placenta Diseases,,,,,,,D010922,,,,
+BMGC_DS20621,BMG_DS078749,,,Plant Poisoning,,,,,,,D010939,,,,
+BMGC_DS20622,BMG_DS078750,,,Plasmacytoma,,,,,,,D010954,,,,
+BMGC_DS20623,BMG_DS078752,,,Pleural Effusion,,,,,,,D010996,,,,
+BMGC_DS20624,BMG_DS078753,,,Pleural Neoplasms,,,,,,,D010997,,,,
+BMGC_DS20625,BMG_DS078754,,,"Pneumonia, Pneumococcal",,,,,,,D011018,,,,
+BMGC_DS20626,BMG_DS078755,,,"Pneumonia, Pneumocystis",,,,,,,D011020,,,,
+BMGC_DS20627,BMG_DS078756,,,Rothmund-Thomson Syndrome,,,,,,,D011038,,,,
+BMGC_DS20628,BMG_DS078757,,,Poisoning,,,,,,,D011041,,MONDO:0029000,poisoning,
+BMGC_DS20629,BMG_DS078758,,,Polycythemia Vera,,,,,,,D011087,,,,
+BMGC_DS20630,BMG_DS078759,,,Polyploidy,,,,,,,D011123,,,,
+BMGC_DS20631,BMG_DS078760,,,Polyps,,,,,,,D011127,,,,
+BMGC_DS20632,BMG_DS078761,,,Polyuria,,,,,,,D011141,,,,
+BMGC_DS20633,BMG_DS078765,,,Postoperative Complications,,,,,,,D011183,,,,
+BMGC_DS20634,BMG_DS078766,,,Pre-Eclampsia,,,,,,,D011225,,,,
+BMGC_DS20635,BMG_DS078767,,,Precancerous Conditions,,,,,,,D011230,,,,
+BMGC_DS20636,BMG_DS078768,,,Prediabetic State,,,,,,,D011236,,,,
+BMGC_DS20637,BMG_DS078769,,,Pregnancy Complications,,,,,,,D011248,,,,
+BMGC_DS20638,BMG_DS078772,,,"Pregnancy, Ectopic",,,,,,,D011271,,,,
+BMGC_DS20639,BMG_DS078773,,,"Pregnancy, Prolonged",,,,,,,D011273,,,,
+BMGC_DS20640,BMG_DS078776,,,Prenatal Exposure Delayed Effects,,,,,,,D011297,,,,
+BMGC_DS20641,BMG_DS078780,,,Prostatic Neoplasms,,,,,,,D011471,,,,
+BMGC_DS20642,BMG_DS078781,,,Proteinuria,,,,,,,D011507,,,,
+BMGC_DS20643,BMG_DS078782,,,Pruritus,,,,,,,D011537,,,,
+BMGC_DS20644,BMG_DS078787,,,Psychomotor Agitation,,,,,,,D011595,,,,
+BMGC_DS20645,BMG_DS078788,,,Psychomotor Disorders,,,,,,,D011596,,,,
+BMGC_DS20646,BMG_DS078789,,,Psychophysiologic Disorders,,,,,,,D011602,,,,
+BMGC_DS20647,BMG_DS078791,,,"Psychoses, Substance-Induced",,,,,,,D011605,,,,
+BMGC_DS20648,BMG_DS078792,,,Pterygium,,,,,,,D011625,,,,
+BMGC_DS20649,BMG_DS078793,,,"Puberty, Delayed",,,,,,,D011628,,,,
+BMGC_DS20650,BMG_DS078794,,,Pulmonary Edema,,,,,,,D011654,,,,
+BMGC_DS20651,BMG_DS078795,,,Pulmonary Heart Disease,,,,,,,D011660,,,,
+BMGC_DS20652,BMG_DS078798,,,Pulmonary Veno-Occlusive Disease,,,,,,,D011668,,,,
+BMGC_DS20653,BMG_DS078802,,,"Radiation Injuries, Experimental",,,,,,,D011833,,,,
+BMGC_DS20654,BMG_DS078806,,,Hyperacusis,,,,,,,D012001,,,,
+BMGC_DS20655,BMG_DS078807,,,Rectal Fistula,,,,DOID:0060328,anal fistula,,D012003,,,,
+BMGC_DS20656,BMG_DS078808,,,Rectal Neoplasms,,,,,,,D012004,,,,
+BMGC_DS20657,BMG_DS078810,,,Recurrence,,,,,,,D012008,,,,
+BMGC_DS20658,BMG_DS078811,,,"Reflex, Abnormal",,,,,,,D012021,,,,
+BMGC_DS20659,BMG_DS078813,,,Respiratory Hypersensitivity,,,,,,,D012130,,,,
+BMGC_DS20660,BMG_DS078814,,,Respiratory Paralysis,,,,,,,D012133,,,,
+BMGC_DS20661,BMG_DS078815,,,Respiratory Sounds,,,,,,,D012135,,,,
+BMGC_DS20662,BMG_DS078817,,,Retinal Degeneration,,,,,,,D012162,,,,
+BMGC_DS20663,BMG_DS078818,,,Retinal Hemorrhage,,,,,,,D012166,,,,
+BMGC_DS20664,BMG_DS078819,,,Retinoblastoma,,,,,,,D012175,,,,
+BMGC_DS20665,BMG_DS078820,,,Retrograde Degeneration,,,,,,,D012183,,,,
+BMGC_DS20666,BMG_DS078821,,,Retroperitoneal Fibrosis,,,,,,,D012185,,,,
+BMGC_DS20667,BMG_DS078822,,,Retroperitoneal Neoplasms,,,,,,,D012186,,,,
+BMGC_DS20668,BMG_DS078824,,,Rhabdomyolysis,,,,,,,D012206,,MONDO:0005290,obsolete rhabdomyolysis,
+BMGC_DS20669,BMG_DS078825,,,Rhabdomyoma,,,,,,,D012207,,,,
+BMGC_DS20670,BMG_DS078826,,,Rhabdomyosarcoma,,,,,,,D012208,,,,
+BMGC_DS20671,BMG_DS078832,,,Rupture,,,,,,,D012421,,,,
+BMGC_DS20672,BMG_DS078833,,,"Rupture, Spontaneous",,,,,,,D012422,,,,
+BMGC_DS20673,BMG_DS078836,,,Salivary Gland Neoplasms,,,,,,,D012468,,,,
+BMGC_DS20674,BMG_DS078837,,,Salmonella Food Poisoning,,,,,,,D012478,,,,
+BMGC_DS20675,BMG_DS078838,,,Salmonella Infections,,,,,,,D012480,,,,
+BMGC_DS20676,BMG_DS078839,,,Sarcoma,,,,,,,D012509,,,,
+BMGC_DS20677,BMG_DS078842,,,"Sarcoma, Ewing",,,,,,,D012512,,,,
+BMGC_DS20678,BMG_DS078843,,,"Sarcoma, Experimental",,,,,,,D012513,,,,
+BMGC_DS20679,BMG_DS078844,,,"Sarcoma, Kaposi",,,,,,,D012514,,,,
+BMGC_DS20680,BMG_DS078846,,,Osteosarcoma,,,,,,,D012516,,,,
+BMGC_DS20681,BMG_DS078850,,,Sclerosis,,,,,,,D012598,,,,
+BMGC_DS20682,BMG_DS078851,,,Scoliosis,,,,,,,D012600,,,,
+BMGC_DS20683,BMG_DS078852,,,Scotoma,,,,,,,D012607,,,,
+BMGC_DS20684,BMG_DS078853,,,Sebaceous Gland Neoplasms,,,,,,,D012626,,,,
+BMGC_DS20685,BMG_DS078855,,,Self Mutilation,,,,,,,D012652,,,,
+BMGC_DS20686,BMG_DS078858,,,"Sexual Dysfunction, Physiological",,,,,,,D012735,,,,
+BMGC_DS20687,BMG_DS078859,,,Sezary Syndrome,,,,,,,D012751,,,,
+BMGC_DS20688,BMG_DS078860,,,Shock,,,,,,,D012769,,,,
+BMGC_DS20689,BMG_DS078861,,,"Shock, Cardiogenic",,,,,,,D012770,,,,
+BMGC_DS20690,BMG_DS078862,,,"Shock, Hemorrhagic",,,,,,,D012771,,,,
+BMGC_DS20691,BMG_DS078864,,,"Shock, Traumatic",,,,,,,D012774,,,,
+BMGC_DS20692,BMG_DS078866,,,Sigmoid Neoplasms,,,,,,,D012811,,,,
+BMGC_DS20693,BMG_DS078867,,,Signs and Symptoms,,,,,,,D012816,,,,
+BMGC_DS20694,BMG_DS078868,,,"Signs and Symptoms, Digestive",,,,,,,D012817,,,,
+BMGC_DS20695,BMG_DS078869,,,"Signs and Symptoms, Respiratory",,,,,,,D012818,,,,
+BMGC_DS20696,BMG_DS078870,,,Situs Inversus,,,,,,,D012857,,,,
+BMGC_DS20697,BMG_DS078871,,,Skin Abnormalities,,,,,,,D012868,,,,
+BMGC_DS20698,BMG_DS078872,,,Skin Diseases,,,,,,,D012871,,,,
+BMGC_DS20699,BMG_DS078873,,,Skin Manifestations,,,,,,,D012877,,,,
+BMGC_DS20700,BMG_DS078874,,,Skin Neoplasms,,,,,,,D012878,,,,
+BMGC_DS20701,BMG_DS078878,,,Sneezing,,,,,,,D012912,,,,
+BMGC_DS20702,BMG_DS078880,,,Soft Tissue Neoplasms,,,,,,,D012983,,,,
+BMGC_DS20703,BMG_DS078882,,,Spasm,,,,,,,D013035,,,,
+BMGC_DS20704,BMG_DS078883,,,"Spherocytosis, Hereditary",,,,,,,D013103,,,,
+BMGC_DS20705,BMG_DS078884,,,Spinal Cord Injuries,,,,,,,D013119,,MONDO:0043797,spinal cord injury,
+BMGC_DS20706,BMG_DS078886,,,Spinal Curvatures,,,,,,,D013121,,,,
+BMGC_DS20707,BMG_DS078890,,,Splenic Neoplasms,,,,,,,D013160,,,,
+BMGC_DS20708,BMG_DS078892,,,Splenomegaly,,,,,,,D013163,,,,
+BMGC_DS20709,BMG_DS078893,,,"Spondylitis, Ankylosing",,,,,,,D013167,,,,
+BMGC_DS20710,BMG_DS078895,,,Starvation,,,,,,,D013217,,,,
+BMGC_DS20711,BMG_DS078897,,,Stomach Neoplasms,,,,,,,D013274,,,,
+BMGC_DS20712,BMG_DS078898,,,Stomach Ulcer,,,,,,,D013276,,,,
+BMGC_DS20713,BMG_DS078900,,,Subcutaneous Emphysema,,,,,,,D013352,,,,
+BMGC_DS20714,BMG_DS078903,,,Substance Withdrawal Syndrome,,,,,,,D013375,,,,
+BMGC_DS20715,BMG_DS078904,,,Sudden Infant Death,,,,,,,D013398,272120,MONDO:0010086,obsolete sudden infant death syndrome,
+BMGC_DS20716,BMG_DS078905,,,Sunburn,,,,,,,D013471,,,,
+BMGC_DS20717,BMG_DS078907,,,Suppuration,,,,,,,D013492,,,,
+BMGC_DS20718,BMG_DS078909,,,Surgical Wound Infection,,,,,,,D013530,,,,
+BMGC_DS20719,BMG_DS078911,,,Sweat Gland Neoplasms,,,,,,,D013544,,,,
+BMGC_DS20720,BMG_DS078912,,,"Pathological Conditions, Signs and Symptoms",,,,,,,D013568,,,,
+BMGC_DS20721,BMG_DS078913,,,Syndactyly,,,,,,,D013576,,,,
+BMGC_DS20722,BMG_DS078916,,,"Sarcoma, Synovial",,,,,,,D013584,,,,
+BMGC_DS20723,BMG_DS078918,,,Tachycardia,,,,,,,D013610,,,,
+BMGC_DS20724,BMG_DS078919,,,"Tachycardia, Supraventricular",,,,,,,D013617,,,,
+BMGC_DS20725,BMG_DS078920,,,Telangiectasis,,,,,,,D013684,,,,
+BMGC_DS20726,BMG_DS078921,,,Tendon Injuries,,,,,,,D013708,,,,
+BMGC_DS20727,BMG_DS078923,,,Testicular Neoplasms,,,,,,,D013736,,,,
+BMGC_DS20728,BMG_DS078924,,,Tetralogy of Fallot,,,,,,,D013771,,,,
+BMGC_DS20729,BMG_DS078928,,,Thoracic Neoplasms,,,,,,,D013899,,,,
+BMGC_DS20730,BMG_DS078929,,,Thromboembolism,,,,,,,D013923,,,,
+BMGC_DS20731,BMG_DS078930,,,Thrombosis,,,,DOID:0060903,thrombosis,,D013927,,,,
+BMGC_DS20732,BMG_DS078931,,,Thymoma,,,,,,,D013945,,,,
+BMGC_DS20733,BMG_DS078932,,,Thymus Neoplasms,,,,,,,D013953,,,,
+BMGC_DS20734,BMG_DS078934,,,Thyroid Neoplasms,,,,,,,D013964,,,,
+BMGC_DS20735,BMG_DS078935,,,"Thyroiditis, Autoimmune",,,,,,,D013967,,,,
+BMGC_DS20736,BMG_DS078937,,,Tibial Fractures,,,,,,,D013978,,MONDO:0005320,tibia fracture,
+BMGC_DS20737,BMG_DS078938,,,Tobacco Use Disorder,,,,,,,D014029,,,,
+BMGC_DS20738,BMG_DS078939,,,Tongue Neoplasms,,,,,,,D014062,,,,
+BMGC_DS20739,BMG_DS078943,,,Tooth Abnormalities,,,,,,,D014071,,,,
+BMGC_DS20740,BMG_DS078944,,,Tooth Abrasion,,,,,,,D014072,,,,
+BMGC_DS20741,BMG_DS078945,,,Tooth Discoloration,,,,,,,D014075,,,,
+BMGC_DS20742,BMG_DS078953,,,Toothache,,,,,,,D014098,,,,
+BMGC_DS20743,BMG_DS078955,,,Torticollis,,,,,,,D014103,,,,
+BMGC_DS20744,BMG_DS078956,,,Toxemia,,,,,,,D014115,,,,
+BMGC_DS20745,BMG_DS078958,,,Tracheoesophageal Fistula,,,,,,,D014138,,,,
+BMGC_DS20746,BMG_DS078959,,,"Translocation, Genetic",,,,,,,D014178,,,,
+BMGC_DS20747,BMG_DS078960,,,Transposition of Great Vessels,,,,,,,D014188,,,,
+BMGC_DS20748,BMG_DS078962,,,Tremor,,,,,,,D014202,,,,
+BMGC_DS20749,BMG_DS078963,,,,,,,DOID:0050587,trichotillomania,,D014256,,,,
+BMGC_DS20750,BMG_DS078964,,,Trichuriasis,,,,,,,D014257,,,,
+BMGC_DS20751,BMG_DS078966,,,Trisomy,,,,,,,D014314,,,,
+BMGC_DS20752,BMG_DS078968,,,"Truncus Arteriosus, Persistent",,,,,,,D014339,,,,
+BMGC_DS20753,BMG_DS078969,,,Tuberous Sclerosis,,,,,,,D014402,,,,
+BMGC_DS20754,BMG_DS078971,,,"Twins, Conjoined",,,,,,,D014428,,,,
+BMGC_DS20755,BMG_DS078972,,,Ulcer,,,,,,,D014456,,,,
+BMGC_DS20756,BMG_DS078974,,,Unconsciousness,,,,,,,D014474,,,,
+BMGC_DS20757,BMG_DS078975,,,Ureteral Diseases,,,,,,,D014515,,,,
+BMGC_DS20758,BMG_DS078976,,,Ureteral Neoplasms,,,,,,,D014516,,,,
+BMGC_DS20759,BMG_DS078977,,,Ureteral Obstruction,,,,,,,D014517,,,,
+BMGC_DS20760,BMG_DS078980,,,Urinary Calculi,,,,,,,D014545,,,,
+BMGC_DS20761,BMG_DS078982,,,Urinary Incontinence,,,,,,,D014549,,,,
+BMGC_DS20762,BMG_DS078983,,,Urinary Tract Infections,,,,DOID:0080784,urinary tract infection,,D014552,,,,
+BMGC_DS20763,BMG_DS078984,,,Urogenital Abnormalities,,,,,,,D014564,,,,
+BMGC_DS20764,BMG_DS078985,,,Urogenital Neoplasms,,,,,,,D014565,,MONDO:0025370,obsolete urogenital neoplasm,
+BMGC_DS20765,BMG_DS078986,,,Urologic Neoplasms,,,,,,,D014571,,,,
+BMGC_DS20766,BMG_DS078988,,,Uterine Hemorrhage,,,,,,,D014592,,,,
+BMGC_DS20767,BMG_DS078990,,,Uterine Neoplasms,,,,,,,D014594,,,,
+BMGC_DS20768,BMG_DS078992,,,Uterine Rupture,,,,,,,D014597,,,,
+BMGC_DS20769,BMG_DS078994,,,"Uveitis, Anterior",,,,,,,D014606,,,,
+BMGC_DS20770,BMG_DS078996,,,Vaginal Neoplasms,,,,,,,D014625,,,,
+BMGC_DS20771,BMG_DS078997,,,Varicose Veins,,,,,,,D014648,,,,
+BMGC_DS20772,BMG_DS079000,,,Virilism,,,,,,,D014770,,,,
+BMGC_DS20773,BMG_DS079002,,,Vomiting,,,,,,,D014839,,,,
+BMGC_DS20774,BMG_DS079004,,,Vulvar Neoplasms,,,,,,,D014846,,,,
+BMGC_DS20775,BMG_DS079005,,,Wallerian Degeneration,,,,,,,D014855,,,,
+BMGC_DS20776,BMG_DS079006,,,Water-Electrolyte Imbalance,,,,,,,D014883,,,,
+BMGC_DS20777,BMG_DS079007,,,Granulomatosis with Polyangiitis,,,,,,,D014890,,,,
+BMGC_DS20778,BMG_DS079010,,,Wounds and Injuries,,,,,,,D014947,,MONDO:0021178,injury,
+BMGC_DS20779,BMG_DS079013,,,"Wounds, Penetrating",,,,,,,D014950,,,,
+BMGC_DS20780,BMG_DS079017,,,Xeroderma Pigmentosum,,,,,,,D014983,,,,
+BMGC_DS20781,BMG_DS079024,,,Supratentorial Neoplasms,,,,,,,D015173,,,,
+BMGC_DS20782,BMG_DS079026,,,Prolactinoma,,,,,,,D015175,,,,
+BMGC_DS20783,BMG_DS079027,,,Colorectal Neoplasms,,,,,,,D015179,,,,
+BMGC_DS20784,BMG_DS079029,,,"Osteoarthritis, Hip",,,,,,,D015207,,,,
+BMGC_DS20785,BMG_DS079030,,,Smoke Inhalation Injury,,,,,,,D015208,,,,
+BMGC_DS20786,BMG_DS079031,,,"Carcinoma, Merkel Cell",,,,,,,D015266,,,,
+BMGC_DS20787,BMG_DS079032,,,Churg-Strauss Syndrome,,,,,,,D015267,,,,
+BMGC_DS20788,BMG_DS079033,,,Gastrinoma,,,,,,,D015408,,,,
+BMGC_DS20789,BMG_DS079034,,,Reperfusion Injury,,,,,,,D015427,,MONDO:0005203,ischemia reperfusion injury,
+BMGC_DS20790,BMG_DS079035,,,Myocardial Reperfusion Injury,,,,,,,D015428,,,,
+BMGC_DS20791,BMG_DS079036,,,Weight Gain,,,,,,,D015430,,,,
+BMGC_DS20792,BMG_DS079037,,,Weight Loss,,,,,,,D015431,,,,
+BMGC_DS20793,BMG_DS079040,,,"Leukemia, Lymphocytic, Chronic, B-Cell",,,,,,,D015451,,,,
+BMGC_DS20794,BMG_DS079041,,,Precursor B-Cell Lymphoblastic Leukemia-Lymphoma,,,,,,,D015452,,,,
+BMGC_DS20795,BMG_DS079043,,,"Leukemia, T-Cell",,,,,,,D015458,,,,
+BMGC_DS20796,BMG_DS079044,,,"Leukemia-Lymphoma, Adult T-Cell",,,,,,,D015459,,,,
+BMGC_DS20797,BMG_DS079045,,,"Leukemia, Prolymphocytic, T-Cell",,,,,,,D015461,,,,
+BMGC_DS20798,BMG_DS079047,,,"Leukemia, Myelogenous, Chronic, BCR-ABL Positive",,,,,,,D015464,,,,
+BMGC_DS20799,BMG_DS079048,,,"Leukemia, Myeloid, Accelerated Phase",,,,,,,D015465,,,,
+BMGC_DS20800,BMG_DS079051,,,"Leukemia, Myeloid, Acute",,,,,,,D015470,,,,
+BMGC_DS20801,BMG_DS079054,,,"Leukemia, Promyelocytic, Acute",,,,,,,D015473,,,,
+BMGC_DS20802,BMG_DS079055,,,"Leukemia, Myelomonocytic, Chronic",,,,,,,D015477,,,,
+BMGC_DS20803,BMG_DS079056,,,"Leukemia, Myelomonocytic, Acute",,,,,,,D015479,,,,
+BMGC_DS20804,BMG_DS079057,,,Choledochal Cyst,,,,,,,D015529,,,,
+BMGC_DS20805,BMG_DS079058,,,Histiocytosis,,,,,,,D015614,,,,
+BMGC_DS20806,BMG_DS079060,,,"Histiocytosis, Sinus",,,,,,,D015618,,,,
+BMGC_DS20807,BMG_DS079061,,,Respiratory System Abnormalities,,,,,,,D015619,,,,
+BMGC_DS20808,BMG_DS079063,,,Mycotoxicosis,,,,,,,D015651,,MONDO:0042497,mycotoxicosis,
+BMGC_DS20809,BMG_DS079064,,,"Mammary Neoplasms, Animal",,,,,,,D015674,,MONDO:0025483,"mammary neoplasms, animal",
+BMGC_DS20810,BMG_DS079067,,,"Granuloma, Foreign-Body",,,,,,,D015745,,,,
+BMGC_DS20811,BMG_DS079068,,,Abdominal Pain,,,,,,,D015746,,,,
+BMGC_DS20812,BMG_DS079070,,,Aniridia,,,,,,,D015783,,,,
+BMGC_DS20813,BMG_DS079071,,,Retinal Dysplasia,,,,,,,D015792,,,,
+BMGC_DS20814,BMG_DS079074,,,"Substance Abuse, Intravenous",,,,,,,D015819,,,,
+BMGC_DS20815,BMG_DS079076,,,Osteochondroma,,,,,,,D015831,,,,
+BMGC_DS20816,BMG_DS079079,,,Anisocoria,,,,,,,D015875,,,,
+BMGC_DS20817,BMG_DS079080,,,Miosis,,,,,,,D015877,,,,
+BMGC_DS20818,BMG_DS079081,,,Mydriasis,,,,,,,D015878,,,,
+BMGC_DS20819,BMG_DS079082,,,Urinary Retention,,,,,,,D016055,,,,
+BMGC_DS20820,BMG_DS079083,,,"Blood Loss, Surgical",,,,,,,D016063,,,,
+BMGC_DS20821,BMG_DS079085,,,Oligohydramnios,,,,,,,D016104,,,,
+BMGC_DS20822,BMG_DS079086,,,"Albinism, Oculocutaneous",,,,DOID:0050632,oculocutaneous albinism,,D016115,,,,
+BMGC_DS20823,BMG_DS079087,,,"Albinism, Ocular",,,,DOID:0050633,ocular albinism 1,,D016117,,,,
+BMGC_DS20824,BMG_DS079088,,,Spinal Dysraphism,,,,,,,D016135,,,,
+BMGC_DS20825,BMG_DS079089,,,Spina Bifida Occulta,,,,DOID:0080073,spina bifida occulta,,D016136,,,,
+BMGC_DS20826,BMG_DS079090,,,Spina Bifida Cystica,,,,,,,D016137,,,,
+BMGC_DS20827,BMG_DS079091,,,Holoprosencephaly,,,,,,,D016142,,,,
+BMGC_DS20828,BMG_DS079092,,,Oral Fistula,,,,,,,D016155,,,,
+BMGC_DS20829,BMG_DS079093,,,Respiratory Tract Fistula,,,,,,,D016156,,,,
+BMGC_DS20830,BMG_DS079097,,,Tooth Loss,,,,,,,D016388,,,,
+BMGC_DS20831,BMG_DS079098,,,"Lymphoma, B-Cell",,,,,,,D016393,,,,
+BMGC_DS20832,BMG_DS079099,,,"Lymphoma, T-Cell",,,,,,,D016399,,,,
+BMGC_DS20833,BMG_DS079101,,,"Lymphoma, Large B-Cell, Diffuse",,,,DOID:0050745,diffuse large B-cell lymphoma,,D016403,,,,
+BMGC_DS20834,BMG_DS079102,,,"Lymphoma, T-Cell, Cutaneous",,,,DOID:0060061,primary cutaneous T-cell non-Hodgkin lymphoma,,D016410,,MONDO:0000607,primary cutaneous T-cell non-Hodgkin lymphoma,
+BMGC_DS20835,BMG_DS079103,,,"Lymphoma, T-Cell, Peripheral",,,,,,,D016411,,,,
+BMGC_DS20836,BMG_DS079105,,,Bacteremia,,,,,,,D016470,,,,
+BMGC_DS20837,BMG_DS079106,,,"Lymphoma, AIDS-Related",,,,,,,D016483,,,,
+BMGC_DS20838,BMG_DS079108,,,"Pemphigus, Benign Familial",,,,,,,D016506,,,,
+BMGC_DS20839,BMG_DS079110,,,Neurofibromatosis 2,,,,,,,D016518,,,,
+BMGC_DS20840,BMG_DS079111,,,"Cardiac Output, High",,,,,,,D016534,,,,
+BMGC_DS20841,BMG_DS079112,,,Central Nervous System Neoplasms,,,,,,,D016543,,,,
+BMGC_DS20842,BMG_DS079114,,,"Purpura, Thrombocytopenic, Idiopathic",,,,,,,D016553,,,,
+BMGC_DS20843,BMG_DS079116,,,,,,,DOID:0060167,seasonal affective disorder,,D016574,,,,
+BMGC_DS20844,BMG_DS079122,,,"Neoplasms, Second Primary",,,,,,,D016609,,,,
+BMGC_DS20845,BMG_DS079125,,,"Plasma Cell Granuloma, Pulmonary",,,,,,,D016726,,,,
+BMGC_DS20846,BMG_DS079126,,,"Death, Sudden, Cardiac",,,,,,,D016757,,,,
+BMGC_DS20847,BMG_DS079129,,,,,,,DOID:0080158,herpes simplex virus keratitis,,D016849,,,,
+BMGC_DS20848,BMG_DS079130,,,Hypocapnia,,,,,,,D016857,,,,
+BMGC_DS20849,BMG_DS079131,,,Endometrial Neoplasms,,,,,,,D016889,,,,
+BMGC_DS20850,BMG_DS079133,,,IgA Deficiency,,,,,,,D017098,,,,
+BMGC_DS20851,BMG_DS079137,,,"Ophthalmoplegia, Chronic Progressive External",,,,,,,D017246,,,,
+BMGC_DS20852,BMG_DS079138,,,Neurofibromatoses,,,,,,,D017253,,,,
+BMGC_DS20853,BMG_DS079139,,,Leukemic Infiltration,,,,,,,D017254,,,,
+BMGC_DS20854,BMG_DS079142,,,Acneiform Eruptions,,,,,,,D017486,,,,
+BMGC_DS20855,BMG_DS079143,,,"Keratosis, Seborrheic",,,,,,,D017492,,,,
+BMGC_DS20856,BMG_DS079144,,,Hyperpigmentation,,,,,,,D017495,,,,
+BMGC_DS20857,BMG_DS079145,,,Hypopigmentation,,,,,,,D017496,,,,
+BMGC_DS20858,BMG_DS079147,,,Iliac Aneurysm,,,,,,,D017543,,,,
+BMGC_DS20859,BMG_DS079148,,,"Aortic Aneurysm, Abdominal",,,,,,,D017544,,,,
+BMGC_DS20860,BMG_DS079149,,,"Aortic Aneurysm, Thoracic",,,,,,,D017545,,,,
+BMGC_DS20861,BMG_DS079153,,,Neuroectodermal Tumors,,,,,,,D017599,,,,
+BMGC_DS20862,BMG_DS079155,,,Polydactyly,,,,,,,D017689,,,,
+BMGC_DS20863,BMG_DS079158,,,"Lymphoma, Large-Cell, Anaplastic",,,,,,,D017728,,,,
+BMGC_DS20864,BMG_DS079159,,,Lymphomatoid Papulosis,,,,,,,D017731,,,,
+BMGC_DS20865,BMG_DS079164,,,"Limb Deformities, Congenital",,,,,,,D017880,,,,
+BMGC_DS20866,BMG_DS079168,,,Glucose Intolerance,,,,,,,D018149,,,,
+BMGC_DS20867,BMG_DS079171,,,Lymphangioleiomyomatosis,,,,,,,D018192,,,,
+BMGC_DS20868,BMG_DS079176,,,Hepatoblastoma,,,,,,,D018197,,,,
+BMGC_DS20869,BMG_DS079179,,,"Mixed Tumor, Mullerian",,,,,,,D018200,,,,
+BMGC_DS20870,BMG_DS079187,,,"Liposarcoma, Myxoid",,,,,,,D018208,,,,
+BMGC_DS20871,BMG_DS079190,,,"Chondrosarcoma, Mesenchymal",,,,,,,D018211,,,,
+BMGC_DS20872,BMG_DS079191,,,Giant Cell Tumor of Bone,,,,,,,D018212,,,,
+BMGC_DS20873,BMG_DS079192,,,"Neoplasms, Bone Tissue",,,,,,,D018213,,,,
+BMGC_DS20874,BMG_DS079197,,,"Neoplasms, Fibrous Tissue",,,,,,,D018218,,,,
+BMGC_DS20875,BMG_DS079198,,,"Histiocytoma, Benign Fibrous",,,,,,,D018219,,,,
+BMGC_DS20876,BMG_DS079200,,,"Fibromatosis, Abdominal",,,,,,,D018221,,,,
+BMGC_DS20877,BMG_DS079201,,,Desmoid Tumors,,,,,,,D018222,,,,
+BMGC_DS20878,BMG_DS079205,,,Fibroadenoma,,,,,,,D018226,,,,
+BMGC_DS20879,BMG_DS079206,,,"Sarcoma, Clear Cell",,,,,,,D018227,,,,
+BMGC_DS20880,BMG_DS079209,,,"Leiomyoma, Epithelioid",,,,,,,D018230,,,,
+BMGC_DS20881,BMG_DS079211,,,"Rhabdomyosarcoma, Alveolar",,,,,,,D018232,,,,
+BMGC_DS20882,BMG_DS079212,,,"Rhabdomyosarcoma, Embryonal",,,,,,,D018233,,,,
+BMGC_DS20883,BMG_DS079213,,,"Sarcoma, Alveolar Soft Part",,,,,,,D018234,,,,
+BMGC_DS20884,BMG_DS079214,,,Smooth Muscle Tumor,,,,,,,D018235,,,,
+BMGC_DS20885,BMG_DS079215,,,"Carcinoma, Embryonal",,,,,,,D018236,,,,
+BMGC_DS20886,BMG_DS079218,,,Seminoma,,,,,,,D018239,,,,
+BMGC_DS20887,BMG_DS079219,,,Endodermal Sinus Tumor,,,,,,,D018240,,,,
+BMGC_DS20888,BMG_DS079220,,,"Neuroectodermal Tumors, Primitive, Peripheral",,,,,,,D018241,,,,
+BMGC_DS20889,BMG_DS079221,,,"Neuroectodermal Tumors, Primitive",,,,,,,D018242,,,,
+BMGC_DS20890,BMG_DS079222,,,Teratocarcinoma,,,,,,,D018243,,,,
+BMGC_DS20891,BMG_DS079224,,,Adrenocortical Adenoma,,,,,,,D018246,,,,
+BMGC_DS20892,BMG_DS079225,,,"Adenoma, Liver Cell",,,,,,,D018248,,,,
+BMGC_DS20893,BMG_DS079226,,,"Adenoma, Oxyphilic",,,,,,,D018249,,,,
+BMGC_DS20894,BMG_DS079233,,,Adenomatous Polyps,,,,,,,D018256,,,,
+BMGC_DS20895,BMG_DS079235,,,"Adenocarcinoma, Clear Cell",,,,,,,D018262,,,,
+BMGC_DS20896,BMG_DS079236,,,"Adenocarcinoma, Follicular",,,,,,,D018263,,,,
+BMGC_DS20897,BMG_DS079240,,,Adrenocortical Carcinoma,,,,,,,D018268,,,,
+BMGC_DS20898,BMG_DS079241,,,"Carcinoma, Endometrioid",,,,,,,D018269,,,,
+BMGC_DS20899,BMG_DS079242,,,"Carcinoma, Ductal, Breast",,,,,,,D018270,,,,
+BMGC_DS20900,BMG_DS079244,,,"Carcinoma, Lobular",,,,,,,D018275,,,,
+BMGC_DS20901,BMG_DS079245,,,"Carcinoma, Medullary",,,,,,,D018276,,,,
+BMGC_DS20902,BMG_DS079246,,,"Carcinoma, Mucoepidermoid",,,,,,,D018277,,,,
+BMGC_DS20903,BMG_DS079250,,,Cholangiocarcinoma,,,,,,,D018281,,,,
+BMGC_DS20904,BMG_DS079256,,,"Carcinoma, Large Cell",,,,,,,D018287,,,,
+BMGC_DS20905,BMG_DS079257,,,"Carcinoma, Small Cell",,,,,,,D018288,,,,
+BMGC_DS20906,BMG_DS079264,,,Pilomatrixoma,,,,,,,D018296,,,,
+BMGC_DS20907,BMG_DS079269,,,"Neoplasms, Mesothelial",,,,,,,D018301,,,,
+BMGC_DS20908,BMG_DS079275,,,"Neoplasms, Squamous Cell",,,,,,,D018307,,,,
+BMGC_DS20909,BMG_DS079282,,,Gliosarcoma,,,,,,,D018316,,,,
+BMGC_DS20910,BMG_DS079283,,,Nerve Sheath Neoplasms,,,,,,,D018317,,,,
+BMGC_DS20911,BMG_DS079284,,,"Neurofibroma, Plexiform",,,,,,,D018318,,,,
+BMGC_DS20912,BMG_DS079285,,,Neurofibrosarcoma,,,,,,,D018319,,,,
+BMGC_DS20913,BMG_DS079288,,,"Hemangioendothelioma, Epithelioid",,,,,,,D018323,,,,
+BMGC_DS20914,BMG_DS079290,,,Hemangioblastoma,,,,,,,D018325,,,,
+BMGC_DS20915,BMG_DS079291,,,Nevi and Melanomas,,,,,,,D018326,,,,
+BMGC_DS20916,BMG_DS079293,,,"Melanoma, Amelanotic",,,,,,,D018328,,,,
+BMGC_DS20917,BMG_DS079297,,,"Nevus, Epithelioid and Spindle Cell",,,,,,,D018332,,,,
+BMGC_DS20918,BMG_DS079299,,,Rhabdoid Tumor,,,,,,,D018335,,,,
+BMGC_DS20919,BMG_DS079300,,,Neuroendocrine Tumors,,,,,,,D018358,,,,
+BMGC_DS20920,BMG_DS079301,,,"Neoplasm, Residual",,,,,,,D018365,,,,
+BMGC_DS20921,BMG_DS079302,,,Cardiovascular Abnormalities,,,,,,,D018376,,,,
+BMGC_DS20922,BMG_DS079305,,,"Lymphoma, B-Cell, Marginal Zone",,,,DOID:0050748,marginal zone lymphoma,,D018442,,,,
+BMGC_DS20923,BMG_DS079306,,,Disease Progression,,,,,,,D018450,,,,
+BMGC_DS20924,BMG_DS079308,,,Hypokinesia,,,,,,,D018476,,,,
+BMGC_DS20925,BMG_DS079309,,,"Ventricular Dysfunction, Left",,,,,,,D018487,,,,
+BMGC_DS20926,BMG_DS079310,,,Hyperoxia,,,,,,,D018496,,,,
+BMGC_DS20927,BMG_DS079311,,,"Ventricular Dysfunction, Right",,,,,,,D018497,,,,
+BMGC_DS20928,BMG_DS079312,,,"Breast Neoplasms, Male",,,,,,,D018567,,,,
+BMGC_DS20929,BMG_DS079315,,,"Vitreoretinopathy, Proliferative",,,,,,,D018630,,,,
+BMGC_DS20930,BMG_DS079317,,,Stomatognathic System Abnormalities,,,,,,,D018640,,,,
+BMGC_DS20931,BMG_DS079318,,,Tooth Injuries,,,,,,,D018677,,,,
+BMGC_DS20932,BMG_DS079319,,,Ventricular Dysfunction,,,,,,,D018754,,,,
+BMGC_DS20933,BMG_DS079320,,,Multiple Endocrine Neoplasia Type 1,,,,,,,D018761,,,,
+BMGC_DS20934,BMG_DS079321,,,Tricuspid Atresia,,,,DOID:0080169,tricuspid atresia,,D018785,,,,
+BMGC_DS20935,BMG_DS079322,,,"Anemia, Iron-Deficiency",,,,,,,D018798,,,,
+BMGC_DS20936,BMG_DS079323,,,Multiple Endocrine Neoplasia Type 2a,,,,,,,D018813,,,,
+BMGC_DS20937,BMG_DS079324,,,Multiple Endocrine Neoplasia Type 2b,,,,,,,D018814,,,,
+BMGC_DS20938,BMG_DS079325,,,"Carcinoma, Lewis Lung",,,,,,,D018827,,,,
+BMGC_DS20939,BMG_DS079326,,,Ventricular Premature Complexes,,,,,,,D018879,,,,
+BMGC_DS20940,BMG_DS079327,,,Heat Stress Disorders,,,,,,,D018882,,,,
+BMGC_DS20941,BMG_DS079328,,,Heat Stroke,,,,,,,D018883,,,,
+BMGC_DS20942,BMG_DS079331,,,Muscle Weakness,,,,,,,D018908,,,,
+BMGC_DS20943,BMG_DS079333,,,Vascular Neoplasms,,,,,,,D019043,,,,
+BMGC_DS20944,BMG_DS079334,,,Bone Marrow Neoplasms,,,,,,,D019046,,,,
+BMGC_DS20945,BMG_DS079335,,,Prostatic Intraepithelial Neoplasia,,,,,,,D019048,,,,
+BMGC_DS20946,BMG_DS079337,,,Facies,,,,,,,D019066,,,,
+BMGC_DS20947,BMG_DS079338,,,Cafe-au-Lait Spots,,,,,,,D019080,,,,
+BMGC_DS20948,BMG_DS079339,,,Postoperative Hemorrhage,,,,,,,D019106,,,,
+BMGC_DS20949,BMG_DS079344,,,Pseudolymphoma,,,,,,,D019310,,,,
+BMGC_DS20950,BMG_DS079346,,,Hematologic Neoplasms,,,,,,,D019337,,,,
+BMGC_DS20951,BMG_DS079347,,,Port-Wine Stain,,,,,,,D019339,,,,
+BMGC_DS20952,BMG_DS079348,,,Chromosome Breakage,,,,,,,D019457,,,,
+BMGC_DS20953,BMG_DS079349,,,Craniofacial Abnormalities,,,,,,,D019465,,,,
+BMGC_DS20954,BMG_DS079351,,,Neck Pain,,,,,,,D019547,,,,
+BMGC_DS20955,BMG_DS079355,,,Multiple System Atrophy,,,,,,,D019578,,,,
+BMGC_DS20956,BMG_DS079356,,,Hot Flashes,,,,,,,D019584,,,,
+BMGC_DS20957,BMG_DS079357,,,Intracranial Hypertension,,,,,,,D019586,,,,
+BMGC_DS20958,BMG_DS079358,,,"Aging, Premature",,,,,,,D019588,,,,
+BMGC_DS20959,BMG_DS079361,,,Maxillofacial Abnormalities,,,,,,,D019767,,,,
+BMGC_DS20960,BMG_DS079363,,,Neurobehavioral Manifestations,,,,,,,D019954,,,,
+BMGC_DS20961,BMG_DS079364,,,Substance-Related Disorders,,,,,,,D019966,,,,
+BMGC_DS20962,BMG_DS079365,,,Amphetamine-Related Disorders,,,,,,,D019969,,,,
+BMGC_DS20963,BMG_DS079366,,,Cocaine-Related Disorders,,,,,,,D019970,,,,
+BMGC_DS20964,BMG_DS079367,,,Genetic Predisposition to Disease,,,,,,,D020022,,,,
+BMGC_DS20965,BMG_DS079370,,,Neurogenic Inflammation,,,,,,,D020078,,,,
+BMGC_DS20966,BMG_DS079371,,,Acquired Hyperostosis Syndrome,,,,,,,D020083,,,,
+BMGC_DS20967,BMG_DS079373,,,Putaminal Hemorrhage,,,,,,,D020146,,,,
+BMGC_DS20968,BMG_DS079374,,,Manganese Poisoning,,,,,,,D020149,,MONDO:0017638,manganese poisoning,
+BMGC_DS20969,BMG_DS079375,,,Ornithine Carbamoyltransferase Deficiency Disease,,,,,,,D020163,,,,
+BMGC_DS20970,BMG_DS079378,,,"Trauma, Nervous System",,,,,,,D020196,,MONDO:0044745,nervous system injury,
+BMGC_DS20971,BMG_DS079380,,,"Intracranial Hemorrhage, Traumatic",,,,,,,D020198,,,,
+BMGC_DS20972,BMG_DS079381,,,"Hematoma, Subdural, Acute",,,,,,,D020199,,,,
+BMGC_DS20973,BMG_DS079382,,,"Hematoma, Subdural, Chronic",,,,,,,D020200,,,,
+BMGC_DS20974,BMG_DS079383,,,"Brain Hemorrhage, Traumatic",,,,,,,D020201,,,,
+BMGC_DS20975,BMG_DS079392,,,Cerebrovascular Trauma,,,,,,,D020214,,MONDO:0005621,vascular brain injury,
+BMGC_DS20976,BMG_DS079395,,,Optic Nerve Injuries,,,,,,,D020221,,,,
+BMGC_DS20977,BMG_DS079397,,,Serotonin Syndrome,,,,,,,D020230,,,,
+BMGC_DS20978,BMG_DS079399,,,Gait Ataxia,,,,,,,D020234,,,,
+BMGC_DS20979,BMG_DS079400,,,"Amnesia, Transient Global",,,,,,,D020236,,,,
+BMGC_DS20980,BMG_DS079404,,,Postoperative Nausea and Vomiting,,,,,,,D020250,,,,
+BMGC_DS20981,BMG_DS079405,,,Choroidal Neovascularization,,,,,,,D020256,,,,
+BMGC_DS20982,BMG_DS079406,,,Ventricular Remodeling,,,,,,,D020257,,,,
+BMGC_DS20983,BMG_DS079407,,,Neurotoxicity Syndromes,,,,,,,D020258,,MONDO:0005527,toxic encephalopathy,
+BMGC_DS20984,BMG_DS079408,,,"Heavy Metal Poisoning, Nervous System",,,,,,,D020260,,,,
+BMGC_DS20985,BMG_DS079409,,,"Lead Poisoning, Nervous System",,,,,,,D020263,,,,
+BMGC_DS20986,BMG_DS079410,,,"Papilloma, Choroid Plexus",,,,,,,D020288,,,,
+BMGC_DS20987,BMG_DS079411,,,Brain Stem Neoplasms,,,,,,,D020295,,,,
+BMGC_DS20988,BMG_DS079413,,,Intracranial Hemorrhages,,,,,,,D020300,,MONDO:0005049,obsolete intracranial hemorrhage,
+BMGC_DS20989,BMG_DS079415,,,Tics,,,,,,,D020323,,,,
+BMGC_DS20990,BMG_DS079417,,,Paraparesis,,,,,,,D020335,,,,
+BMGC_DS20991,BMG_DS079418,,,"Paraparesis, Spastic",,,,,,,D020336,,,,
+BMGC_DS20992,BMG_DS079420,,,Lithiasis,,,,,,,D020347,,,,
+BMGC_DS20993,BMG_DS079422,,,"Nystagmus, Congenital",,,,,,,D020417,,,,
+BMGC_DS20994,BMG_DS079423,,,Olfactory Nerve Diseases,,,,,,,D020431,,,,
+BMGC_DS20995,BMG_DS079425,,,Hypokalemic Periodic Paralysis,,,,,,,D020514,,,,
+BMGC_DS20996,BMG_DS079426,,,Fetal Weight,,,,,,,D020567,,,,
+BMGC_DS20997,BMG_DS079429,,,Amaurosis Fugax,,,,,,,D020757,,,,
+BMGC_DS20998,BMG_DS079430,,,"Pathological Conditions, Anatomical",,,,,,,D020763,,,,
+BMGC_DS20999,BMG_DS079432,,,"Hemangioma, Cavernous, Central Nervous System",,,,,,,D020786,,,,
+BMGC_DS21000,BMG_DS079435,,,Photophobia,,,,,,,D020795,,,,
+BMGC_DS21001,BMG_DS079438,,,Neuromuscular Manifestations,,,,,,,D020879,,,,
+BMGC_DS21002,BMG_DS079439,,,Hypovolemia,,,,,,,D020896,,,,
+BMGC_DS21003,BMG_DS079440,,,Korsakoff Syndrome,,,,,,,D020915,,,,
+BMGC_DS21004,BMG_DS079442,,,Embryo Loss,,,,,,,D020964,,,,
+BMGC_DS21005,BMG_DS079444,,,Wheat Hypersensitivity,,,,,,,D021182,,MONDO:0007021,obsolete wheat allergic disease,
+BMGC_DS21006,BMG_DS079445,,,Peanut Hypersensitivity,,,,,,,D021183,,MONDO:0005902,obsolete peanut allergic reaction,
+BMGC_DS21007,BMG_DS079446,,,"Carcinoma, Pancreatic Ductal",,,,,,,D021441,,,,
+BMGC_DS21008,BMG_DS079447,,,Flank Pain,,,,,,,D021501,,,,
+BMGC_DS21009,BMG_DS079448,,,"Aortic Stenosis, Supravalvular",,,,,,,D021921,,,,
+BMGC_DS21010,BMG_DS079449,,,Hyperammonemia,,,,,,,D022124,,,,
+BMGC_DS21011,BMG_DS079451,,,Chills,,,,,,,D023341,,,,
+BMGC_DS21012,BMG_DS079452,,,,,,,,,,D023521;D002690,,MONDO:0021697,chlamydia infectious disease,
+BMGC_DS21013,BMG_DS079453,,,"Gonadal Dysgenesis, 46,XX",,,,,,,D023961,,,,
+BMGC_DS21014,BMG_DS079458,,,"Anemia, Hypoplastic, Congenital",,,,,,,D029502,,,,
+BMGC_DS21015,BMG_DS079460,,,Papillomavirus Infections,,,,DOID:11166,Human papillomavirus infectious disease,,D030361,,,,
+BMGC_DS21016,BMG_DS079463,,,Gestational Trophoblastic Disease,,,,,,,D031901,,MONDO:0016784,obsolete gestational trophoblastic disease,
+BMGC_DS21017,BMG_DS079465,,,Hearing Loss,,,,,,,D034381,,,,
+BMGC_DS21018,BMG_DS079466,,,"Mastocytosis, Systemic",,,,,,,D034721,,,,
+BMGC_DS21019,BMG_DS079469,,,Ciguatera Poisoning,,,,,,,D036841,,MONDO:0043230,ciguatera fish poisoning,
+BMGC_DS21020,BMG_DS079472,,,"Lower Extremity Deformities, Congenital",,,,,,,D038061,,,,
+BMGC_DS21021,BMG_DS079473,,,"Upper Extremity Deformities, Congenital",,,,,,,D038062,,,,
+BMGC_DS21022,BMG_DS079475,,,X-Linked Intellectual Disability,,,,,,,D038901,,,,
+BMGC_DS21023,BMG_DS079476,,,Coffin-Lowry Syndrome,,,,,,,D038921,,,,
+BMGC_DS21024,BMG_DS079477,,,Genomic Instability,,,,,,,D042822,,,,
+BMGC_DS21025,BMG_DS079478,,,Gallstones,,,,,,,D042882,,,,
+BMGC_DS21026,BMG_DS079479,,,Chromosomal Instability,,,,,,,D043171,,,,
+BMGC_DS21027,BMG_DS079482,,,Lymphatic Abnormalities,,,,,,,D044148,,,,
+BMGC_DS21028,BMG_DS079483,,,"Carcinoma, Ductal",,,,,,,D044584,,,,
+BMGC_DS21029,BMG_DS079484,,,Reticulocytosis,,,,,,,D045262,,,,
+BMGC_DS21030,BMG_DS079489,,,"Hypertension, Pregnancy-Induced",,,,,,,D046110,,,,
+BMGC_DS21031,BMG_DS079491,,,Gastrointestinal Stromal Tumors,,,,,,,D046152,,,,
+BMGC_DS21032,BMG_DS079492,,,"Hernia, Abdominal",,,,,,,D046449,,,,
+BMGC_DS21033,BMG_DS079497,,,"Hematoma, Epidural, Spinal",,,,,,,D046748,,,,
+BMGC_DS21034,BMG_DS079502,,,Premature Birth,,,,,,,D047928,,,,
+BMGC_DS21035,BMG_DS079503,,,Hepatic Insufficiency,,,,,,,D048550,,,,
+BMGC_DS21036,BMG_DS079504,,,"Micronuclei, Chromosome-Defective",,,,,,,D048629,,,,
+BMGC_DS21037,BMG_DS079507,,,"Plagiocephaly, Nonsynostotic",,,,,,,D049068,,,,
+BMGC_DS21038,BMG_DS079508,,,Prenatal Injuries,,,,,,,D049188,,,,
+BMGC_DS21039,BMG_DS079514,,,Growth Hormone-Secreting Pituitary Adenoma,,,,,,,D049912,,,,
+BMGC_DS21040,BMG_DS079515,,,ACTH-Secreting Pituitary Adenoma,,,,,,,D049913,,,,
+BMGC_DS21041,BMG_DS079516,,,Overweight,,,,,,,D050177,,,,
+BMGC_DS21042,BMG_DS079520,,,Stillbirth,,,,,,,D050497,,,,
+BMGC_DS21043,BMG_DS079521,,,"Fractures, Bone",,,,,,,D050723,,MONDO:0005315,bone fracture,
+BMGC_DS21044,BMG_DS079524,,,Post-Dural Puncture Headache,,,,,,,D051299,,,,
+BMGC_DS21045,BMG_DS079525,,,Mobility Limitation,,,,,,,D051346,,,,
+BMGC_DS21046,BMG_DS079526,,,"Neuralgia, Postherpetic",,,,,,,D051474,,,,
+BMGC_DS21047,BMG_DS079527,,,Hemospermia,,,,,,,D051516,,,,
+BMGC_DS21048,BMG_DS079530,,,"Histiocytoma, Malignant Fibrous",,,,,,,D051677,,,,
+BMGC_DS21049,BMG_DS079532,,,Mucositis,,,,DOID:0080178,mucositis,,D052016,,,,
+BMGC_DS21050,BMG_DS079537,,,Dysuria,,,,,,,D053159,,,,
+BMGC_DS21051,BMG_DS079539,,,Nocturnal Enuresis,,,,,,,D053206,,,,
+BMGC_DS21052,BMG_DS079541,,,"Ectodermal Dysplasia 1, Anhidrotic",,,,,,,D053358,,,,
+BMGC_DS21053,BMG_DS079542,,,"Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive",,,,,,,D053360,,,,
+BMGC_DS21054,BMG_DS079545,,,Ichthyosis Bullosa of Siemens,,,,,,,D053560,,,,
+BMGC_DS21055,BMG_DS079546,,,Hypercalciuria,,,,,,,D053565,,,,
+BMGC_DS21056,BMG_DS079550,,,Stupor,,,,,,,D053608,,,,
+BMGC_DS21057,BMG_DS079551,,,Lethargy,,,,,,,D053609,,,,
+BMGC_DS21058,BMG_DS079552,,,Aspermia,,,,,,,D053714,,,,
+BMGC_DS21059,BMG_DS079554,,,Microsatellite Instability,,,,,,,D053842,,,,
+BMGC_DS21060,BMG_DS079555,,,"Leukemia, Large Granular Lymphocytic",,,,,,,D054066,,,,
+BMGC_DS21061,BMG_DS079556,,,Vascular Malformations,,,,,,,D054079,,,,
+BMGC_DS21062,BMG_DS079559,,,Lissencephaly,,,,,,,D054082,,,,
+BMGC_DS21063,BMG_DS079562,,,Arachnodactyly,,,,,,,D054119,,,,
+BMGC_DS21064,BMG_DS079563,,,"Sinus Arrest, Cardiac",,,,,,,D054138,,,,
+BMGC_DS21065,BMG_DS079565,,,Precursor Cell Lymphoblastic Leukemia-Lymphoma,,,,,,,D054198,,,,
+BMGC_DS21066,BMG_DS079566,,,Precursor T-Cell Lymphoblastic Leukemia-Lymphoma,,,,,,,D054218,,,,
+BMGC_DS21067,BMG_DS079568,,,No-Reflow Phenomenon,,,,,,,D054318,,,,
+BMGC_DS21068,BMG_DS079569,,,Sertoli Cell-Only Syndrome,,,,,,,D054331,305700,MONDO:0056795,X-linked spermatogenic failure 1,
+BMGC_DS21069,BMG_DS079571,,,Solitary Fibrous Tumors,,,,,,,D054364,,,,
+BMGC_DS21070,BMG_DS079572,,,"Lymphoma, Extranodal NK-T-Cell",,,,,,,D054391,,,,
+BMGC_DS21071,BMG_DS079574,,,"Leukemia, Myelomonocytic, Juvenile",,,,,,,D054429,,,,
+BMGC_DS21072,BMG_DS079575,,,Myelodysplastic-Myeloproliferative Diseases,,,,,,,D054437,,MONDO:0020077,myelodysplastic/myeloproliferative disease,
+BMGC_DS21073,BMG_DS079576,,,"Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative",,,,,,,D054438,,,,
+BMGC_DS21074,BMG_DS079580,,,Hyperphosphatemia,,,,,,,D054559,,,,
+BMGC_DS21075,BMG_DS079585,,,Histiocytic Sarcoma,,,,DOID:0080915,histiocytic sarcoma,,D054747,,,,
+BMGC_DS21076,BMG_DS079587,,,Primary Dysautonomias,,,,,,,D054969,,MONDO:0021809,primary dysautonomia,
+BMGC_DS21077,BMG_DS079588,,,Orthostatic Intolerance,,,,,,,D054971,,,,
+BMGC_DS21078,BMG_DS079590,,,Pallister-Hall Syndrome,,,,,,,D054975,,,,
+BMGC_DS21079,BMG_DS079591,,,Primary Graft Dysfunction,,,,,,,D055031,,,,
+BMGC_DS21080,BMG_DS079594,,,Delayed Emergence from Anesthesia,,,,,,,D055191,,,,
+BMGC_DS21081,BMG_DS079596,,,Acute Lung Injury,,,,,,,D055371,,MONDO:0015796,acute lung injury,
+BMGC_DS21082,BMG_DS079600,,,"Keratosis, Actinic",,,,,,,D055623,,,,
+BMGC_DS21083,BMG_DS079601,,,Muir-Torre Syndrome,,,,,,,D055653,,,,
+BMGC_DS21084,BMG_DS079602,,,Primary Myelofibrosis,,,,,,,D055728,,,,
+BMGC_DS21085,BMG_DS079603,,,Small Cell Lung Carcinoma,,,,,,,D055752,,,,
+BMGC_DS21086,BMG_DS079605,,,Lynch Syndrome II,,,,,,,D055847,,,,
+BMGC_DS21087,BMG_DS079614,,,"Obesity, Abdominal",,,,,,,D056128,,,,
+BMGC_DS21088,BMG_DS079616,,,Airway Remodeling,,,,,,,D056151,,,,
+BMGC_DS21089,BMG_DS079622,,,Costello Syndrome,,,,,,,D056685,,,,
+BMGC_DS21090,BMG_DS079623,,,Silver-Russell Syndrome,,,,,,,D056730,,,,
+BMGC_DS21091,BMG_DS079624,,,Prolidase Deficiency,,,,,,,D056732,,,,
+BMGC_DS21092,BMG_DS079625,,,Monilethrix,,,,,,,D056734,,,,
+BMGC_DS21093,BMG_DS079626,,,Renal Colic,,,,,,,D056844,,,,
+BMGC_DS21094,BMG_DS079628,,,Barth Syndrome,,,,,,,D056889,,,,
+BMGC_DS21095,BMG_DS079634,,,Shellfish Poisoning,,,,,,,D057096,,,,
+BMGC_DS21096,BMG_DS079637,,,Wet Macular Degeneration,,,,,,,D057135,,,,
+BMGC_DS21097,BMG_DS079638,,,Frontotemporal Lobar Degeneration,,,,,,,D057174,,,,
+BMGC_DS21098,BMG_DS079640,,,Frontotemporal Dementia,,,,,,,D057180,,,,
+BMGC_DS21099,BMG_DS079642,,,Eosinophilic Esophagitis,,,,,,,D057765,,,,
+BMGC_DS21100,BMG_DS079644,,,Vascular System Injuries,,,,,,,D057772,,,,
+BMGC_DS21101,BMG_DS079656,,,Dent Disease,,,,,,,D057973,,,,
+BMGC_DS21102,BMG_DS079657,,,"Plaque, Amyloid",,,,,,,D058225,,,,
+BMGC_DS21103,BMG_DS079658,,,"Plaque, Atherosclerotic",,,,,,,D058226,,,,
+BMGC_DS21104,BMG_DS079659,,,Tungiasis,,,,DOID:0050266,tungiasis,,D058285,,,,
+BMGC_DS21105,BMG_DS079661,,,Desmoplastic Small Round Cell Tumor,,,,,,,D058405,,,,
+BMGC_DS21106,BMG_DS079662,,,Neointima,,,,,,,D058426,,,,
+BMGC_DS21107,BMG_DS079664,,,Eye Pain,,,,,,,D058447,,,,
+BMGC_DS21108,BMG_DS079665,,,Retinal Telangiectasis,,,,,,,D058456,,,,
+BMGC_DS21109,BMG_DS079666,,,Sotos Syndrome,,,,,,,D058495,,,,
+BMGC_DS21110,BMG_DS079667,,,Smith-Magenis Syndrome,,,,DOID:0060768,Smith-Magenis syndrome,,D058496,,,,
+BMGC_DS21111,BMG_DS079668,,,Fraser Syndrome,,,,DOID:0090001,Fraser syndrome,,D058497,,,,
+BMGC_DS21112,BMG_DS079669,,,Enteropathy-Associated T-Cell Lymphoma,,,,,,,D058527,,,,
+BMGC_DS21113,BMG_DS079676,,,Megalencephaly,,,,,,,D058627,,,,
+BMGC_DS21114,BMG_DS079682,,,Aberrant Crypt Foci,,,,,,,D058739,,,,
+BMGC_DS21115,BMG_DS079683,,,Inflammatory Breast Neoplasms,,,,,,,D058922,,,,
+BMGC_DS21116,BMG_DS079686,,,Nociceptive Pain,,,,,,,D059226,,,,
+BMGC_DS21117,BMG_DS079688,,,Tachypnea,,,,,,,D059246,,,,
+BMGC_DS21118,BMG_DS079691,,,Brachydactyly,,,,DOID:0050581,brachydactyly,,D059327,,,,
+BMGC_DS21119,BMG_DS079692,,,Peripheral Nerve Injuries,,,,,,,D059348,,,,
+BMGC_DS21120,BMG_DS079693,,,Musculoskeletal Pain,,,,,,,D059352,,,,
+BMGC_DS21121,BMG_DS079694,,,Mastodynia,,,,,,,D059373,,,,
+BMGC_DS21122,BMG_DS079698,,,Anhedonia,,,,,,,D059445,,,,
+BMGC_DS21123,BMG_DS079700,,,Polydipsia,,,,,,,D059606,,,,
+BMGC_DS21124,BMG_DS079706,,,"Angina, Stable",,,,,,,D060050,,,,
+BMGC_DS21125,BMG_DS079710,,,Dyscalculia,,,,DOID:12568,dyscalculia,,D060705,,,,
+BMGC_DS21126,BMG_DS079717,,,Agenesis of Corpus Callosum,,,,,,,D061085,,,,
+BMGC_DS21127,BMG_DS079718,,,Vascular Calcification,,,,,,,D061205,,,,
+BMGC_DS21128,BMG_DS079719,,,Neoplasm Micrometastasis,,,,,,,D061206,,,,
+BMGC_DS21129,BMG_DS079733,,,Hereditary Breast and Ovarian Cancer Syndrome,,,,,,,D061325,,,,
+BMGC_DS21130,BMG_DS079736,,,Organophosphate Poisoning,,,,,,,D062025,,,,
+BMGC_DS21131,BMG_DS079739,,,Steatocystoma Multiplex,,,,DOID:0111556,steatocystoma multiplex,,D062685,,,,
+BMGC_DS21132,BMG_DS079741,,,Lipoblastoma,,,,,,,D062689,,,,
+BMGC_DS21133,BMG_DS079743,,,Drug Overdose,,,,,,,D062787,,,,
+BMGC_DS21134,BMG_DS079745,,,Maternal Death,,,,,,,D063130,,,,
+BMGC_DS21135,BMG_DS079747,,,Retrognathia,,,,,,,D063173,,,,
+BMGC_DS21136,BMG_DS079749,,,Binge Drinking,,,,,,,D063425,,,,
+BMGC_DS21137,BMG_DS079752,,,Carcinogenesis,,,,,,,D063646,,,,
+BMGC_DS21138,BMG_DS079753,,,Myalgia,,,,,,,D063806,,,,
+BMGC_DS21139,BMG_DS079756,,,"Prostatic Neoplasms, Castration-Resistant",,,,DOID:0080909,castration-resistant prostate carcinoma,,D064129,,,,
+BMGC_DS21140,BMG_DS079760,,,Chemically-Induced Disorders,,,,,,,D064419,,MONDO:0029001,obsolete chemically-induced disorder,
+BMGC_DS21141,BMG_DS079761,,,Drug-Related Side Effects and Adverse Reactions,,,,,,,D064420,,,,
+BMGC_DS21142,BMG_DS079762,,,Triple Negative Breast Neoplasms,,,,,,,D064726,,,,
+BMGC_DS21143,BMG_DS079765,,,Teratogenesis,,,,,,,D064793,,,,
+BMGC_DS21144,BMG_DS079771,,,Corneal Injuries,,,,,,,D065306,,,,
+BMGC_DS21145,BMG_DS079778,,,"Hernias, Diaphragmatic, Congenital",,,,,,,D065630,,,,
+BMGC_DS21146,BMG_DS079779,,,"Rhinitis, Allergic",,,,,,,D065631,,,,
+BMGC_DS21147,BMG_DS079781,,,"Thyroid Carcinoma, Anaplastic",,,,,,,D065646,,,,
+BMGC_DS21148,BMG_DS079784,,,Polymicrogyria,,,,DOID:0080918,polymicrogyria,,D065706,,,,
+BMGC_DS21149,BMG_DS079785,,,Schizencephaly,,,,,,,D065707,,,,
+BMGC_DS21150,BMG_DS079787,,,Congenital Microtia,,,,,,,D065817,,,,
+BMGC_DS21151,BMG_DS079789,,,Perinatal Death,,,,,,,D066087,,,,
+BMGC_DS21152,BMG_DS079790,,,Infant Death,,,,,,,D066088,,,,
+BMGC_DS21153,BMG_DS079791,,,Cardiotoxicity,,,,,,,D066126,,,,
+BMGC_DS21154,BMG_DS079794,,,Vascular Remodeling,,,,,,,D066253,,,,
+BMGC_DS21155,BMG_DS079795,,,"Protein Aggregation, Pathological",,,,,,,D066263,,,,
+BMGC_DS21156,BMG_DS079796,,,,,,,DOID:0050606,acrokeratosis verruciformis,,,101900,,,
+BMGC_DS21157,BMG_DS079797,,,,,,,DOID:0050762,adenylosuccinase lyase deficiency,,,103050,,,
+BMGC_DS21158,BMG_DS079798,,,,,,,DOID:0080053,pseudohypoparathyroidism type 1A,,,103580,,,
+BMGC_DS21159,BMG_DS079799,,,,,,,DOID:0050741,alcohol dependence,,,103780,,,
+BMGC_DS21160,BMG_DS079800,,,,,,,DOID:0050637,Finnish type amyloidosis,,,105120,,,
+BMGC_DS21161,BMG_DS079801,,,,,,,DOID:0070027,CST3-related cerebral amyloid angiopathy,,,105150,,,
+BMGC_DS21162,BMG_DS079802,,,,,,,DOID:0050636,familial visceral amyloidosis,,,105200,,,
+BMGC_DS21163,BMG_DS079803,,,,,,,DOID:0080964,intracranial berry aneurysm 1,,,105800,,,
+BMGC_DS21164,BMG_DS079804,,,,,,,DOID:0080939,hereditary angioedema type I,,,106100,,,
+BMGC_DS21165,BMG_DS079805,,,,,,,DOID:0060603,isolated anhidrosis with normal sweat glands,,,106190,,,
+BMGC_DS21166,BMG_DS079806,,,,,,,DOID:0070532,aniridia 1,,,106210,,,
+BMGC_DS21167,BMG_DS079807,,,,,,,DOID:0080603,ankylosing spondylitis 1,,,106300,,,
+BMGC_DS21168,BMG_DS079808,,,,,,,DOID:0080661,nonsyndromic aplasia cutis congenita,,,107600,,,
+BMGC_DS21169,BMG_DS079809,,,,,,,DOID:0080676,Stickler syndrome 1,,,108300,,,
+BMGC_DS21170,BMG_DS079810,,,,,,,DOID:0070164,spermatogenic failure 2,,,108420,,,
+BMGC_DS21171,BMG_DS079811,,,,,,,DOID:0050772,spastic ataxia 1,,,108600,,,
+BMGC_DS21172,BMG_DS079812,,,,,,,DOID:0050945,spastic ataxia 7,,,108650,,,
+BMGC_DS21173,BMG_DS079813,,,,,,,DOID:0050648,atelosteogenesis,,,108720;108721;256050,,,
+BMGC_DS21174,BMG_DS079814,,,,,,,DOID:0050801,androgenic alopecia,,,109200;300710;612421,,,
+BMGC_DS21175,BMG_DS079815,,,,,,,DOID:0070365,nevoid basal cell carcinoma syndrome 1,,,109400,,,
+BMGC_DS21176,BMG_DS079816,,,,,,,DOID:0070358,primary biliary cholangitis 1,,,109720,,,
+BMGC_DS21177,BMG_DS079817,,,,,,,DOID:0080333,aortic valve disease 1,,,109730,,,
+BMGC_DS21178,BMG_DS079818,,,,,,,DOID:0110969,brachydactyly type B1,,,113000,,,
+BMGC_DS21179,BMG_DS079819,,,,,,,DOID:0110971,brachydactyly type D,,,113200,,,
+BMGC_DS21180,BMG_DS079820,,,,,,,DOID:0110972,brachydactyly type E1,,,113300,,,
+BMGC_DS21181,BMG_DS079821,,,,,,,DOID:0050691,branchiooculofacial syndrome,,,113620,,,
+BMGC_DS21182,BMG_DS079822,,,,,,,DOID:0111423,branchiootorenal syndrome 1,,,113650,,,
+BMGC_DS21183,BMG_DS079823,,,,,,,DOID:0111074,progressive familial heart block type IA,,,113900,,,
+BMGC_DS21184,BMG_DS079824,,,,,,,DOID:0050925,small intestine carcinoid neuroendocrine tumor,,,114900,,,
+BMGC_DS21185,BMG_DS079825,,,,,,,DOID:0111073,progressive familial heart block,,,115080;PS113900,,,
+BMGC_DS21186,BMG_DS079826,,,,,,,DOID:0111460,cardiofaciocutaneous syndrome 1,,,115150,,,
+BMGC_DS21187,BMG_DS079827,,,,,,,DOID:0110308,hypertrophic cardiomyopathy 2,,,115195,,,
+BMGC_DS21188,BMG_DS079828,,,,,,,DOID:0110309,hypertrophic cardiomyopathy 3,,,115196,,,
+BMGC_DS21189,BMG_DS079829,,,,,,,DOID:0110310,hypertrophic cardiomyopathy 4,,,115197,,,
+BMGC_DS21190,BMG_DS079830,,,,,,,DOID:0110425,dilated cardiomyopathy 1A,,,115200,,,
+BMGC_DS21191,BMG_DS079831,,,,,,,DOID:0111425,restrictive cardiomyopathy 1,,,115210,,,
+BMGC_DS21192,BMG_DS079832,,,,,,,DOID:0080491,cerebral cavernous malformation 1,,,116860,,,
+BMGC_DS21193,BMG_DS079833,,,,,,,DOID:0110910,leukocyte adhesion deficiency 1,,,116920,,,
+BMGC_DS21194,BMG_DS079834,,,,,,,DOID:0050980,spinocerebellar ataxia type 31,,,117210,,,
+BMGC_DS21195,BMG_DS079835,,,,,,,DOID:0070030,ITM2B-related cerebral amyloid angiopathy 2,,,117300,,,
+BMGC_DS21196,BMG_DS079836,,,,,,,DOID:0050978,spinocerebellar ataxia type 29,,,117360,,,
+BMGC_DS21197,BMG_DS079837,,,,,,,DOID:0112103,Sotos syndrome 1,,,117550,,,
+BMGC_DS21198,BMG_DS079838,,,,,,,DOID:0080589,Klippel-Feil syndrome 1,,,118100,,,
+BMGC_DS21199,BMG_DS079839,,,,,,,DOID:0111419,familial chylomicronemia due to inhibition of lipoprotein lipase activity,,,118830,,,
+BMGC_DS21200,BMG_DS079840,,,,,,,DOID:0111005,cone-rod dystrophy 2,,,120970,,,
+BMGC_DS21201,BMG_DS079841,,,,,,,DOID:0111307,familial febrile seizures 1,,,121210,,,
+BMGC_DS21202,BMG_DS079842,,,,,,,DOID:0080530,granular corneal dystrophy 1,,,121900,,,
+BMGC_DS21203,BMG_DS079843,,,,,,,DOID:0080505,Cornelia de Lange syndrome 1,,,122470,,,
+BMGC_DS21204,BMG_DS079844,,,,,,,DOID:0080665,warfarin resistance,,,122700,,,
+BMGC_DS21205,BMG_DS079845,,,,,,,DOID:0080807,autosomal dominant craniodiaphyseal dysplasia,,,122860,,,
+BMGC_DS21206,BMG_DS079846,,,,,,,DOID:0061010,craniosynostosis 1,,,123100,,,
+BMGC_DS21207,BMG_DS079847,,,,,,,DOID:0111338,isolated elevated serum creatine phosphokinase levels,,,123320,,,
+BMGC_DS21208,BMG_DS079848,,,,,,,DOID:0050660,Beare-Stevenson cutis gyrata syndrome,,,123790,,,
+BMGC_DS21209,BMG_DS079849,,,,,,,DOID:0080720,autosomal dominant congenital deafness with onychodystrophy,,,124480,,,
+BMGC_DS21210,BMG_DS079850,,,,,,,DOID:0081061,nephrogenic diabetes insipidus type 2,,,125800,,,
+BMGC_DS21211,BMG_DS079851,,,,,,,DOID:0111099,maturity-onset diabetes of the young type 1,,,125850,,,
+BMGC_DS21212,BMG_DS079852,,,,,,,DOID:0111100,maturity-onset diabetes of the young type 2,,,125851,,,
+BMGC_DS21213,BMG_DS079853,,,,,,,DOID:0080723,Kenny-Caffey syndrome type 2,,,127000,,,
+BMGC_DS21214,BMG_DS079854,,,,,,,DOID:0080726,Ehlers-Danlos syndrome classic type 2,,,130010,,,
+BMGC_DS21215,BMG_DS079855,,,,,,,DOID:14756,vascular type Ehlers-Danlos syndrome,,,130050,,,
+BMGC_DS21216,BMG_DS079856,,,,,,,DOID:0080738,Ehlers-Danlos syndrome spondylodysplastic type 1,,,130070,,,
+BMGC_DS21217,BMG_DS079857,,,,,,,DOID:0080224,autosomal dominant dystrophic epidermolysis bullosa,,,131750,,,
+BMGC_DS21218,BMG_DS079858,,,,,,,DOID:0080510,epidermolysis bullosa simplex localized type,,,131800,,,
+BMGC_DS21219,BMG_DS079859,,,,,,,DOID:0080988,pretibial dystrophic epidermolysis bullosa,,,131850,,,
+BMGC_DS21220,BMG_DS079860,,,,,,,DOID:0050981,spinocerebellar ataxia type 34,,,133190,,,
+BMGC_DS21221,BMG_DS079861,,,,,,,DOID:0080908,Cockayne syndrome B,,,133540,,,
+BMGC_DS21222,BMG_DS079862,,,,,,,DOID:0111823,autosomal hemophilia A,,,134500,,,
+BMGC_DS21223,BMG_DS079863,,,,,,,DOID:0081015,congenital fibrosis of the extraocular muscles 1,,,135700,,,
+BMGC_DS21224,BMG_DS079864,,,,,,,DOID:0111357,adermatoglyphia,,,136000,,,
+BMGC_DS21225,BMG_DS079865,,,,,,,DOID:0081045,frontonasal dysplasia 1,,,136760,,,
+BMGC_DS21226,BMG_DS079866,,,,,,,DOID:0050526,Gamstorp-Wohlfart syndrome,,,137200,,,
+BMGC_DS21227,BMG_DS079867,,,,,,,DOID:0050909,extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue,,,137245,,,
+BMGC_DS21228,BMG_DS079868,,,,,,,DOID:0050786,iridogoniodysgenesis syndrome,,,137600;601631,,,
+BMGC_DS21229,BMG_DS079869,,,,,,,DOID:0111101,maturity-onset diabetes of the young type 5,,,137920,,,
+BMGC_DS21230,BMG_DS079870,,,,,,,DOID:0111360,hypotrichosis-lymphedema-telangiectasia-renal defect syndrome,,,137940,,,
+BMGC_DS21231,BMG_DS079871,,,,,,,DOID:0050489,multinodular goiter,,,138800;300273;606082;PS138800,,,
+BMGC_DS21232,BMG_DS079872,,,,,,,DOID:0111363,Heinz body anemia,,,140700,,,
+BMGC_DS21233,BMG_DS079873,,,,,,,DOID:0111365,benign familial hematuria,,,141200,,,
+BMGC_DS21234,BMG_DS079874,,,,,,,DOID:0111366,familial hepatic adenoma,,,142330,,,
+BMGC_DS21235,BMG_DS079875,,,,,,,DOID:0060931,developmental dysplasia of the hip 1,,,142700,,,
+BMGC_DS21236,BMG_DS079876,,,,,,,DOID:0050813,spondyloepiphyseal dysplasia with congenital joint dislocations,,,143095,,,
+BMGC_DS21237,BMG_DS079877,,,,,,,DOID:0070552,epidermolytic palmoplantar keratoderma 1,,,144200,,,
+BMGC_DS21238,BMG_DS079878,,,,,,,DOID:0111421,familial apolipoprotein A5 deficiency,,,144650,,,
+BMGC_DS21239,BMG_DS079879,,,,,,,DOID:0050387,nonpapillary renal cell carcinoma,,,144700,,,
+BMGC_DS21240,BMG_DS079880,,,,,,,DOID:0111373,familial progressive hyperpigmentation with or without hypopigmentation,,,145250,,,
+BMGC_DS21241,BMG_DS079881,,,,,,,DOID:0080698,Teebi hypertelorism syndrome 1,,,145420,,,
+BMGC_DS21242,BMG_DS079882,,,,,,,DOID:0080219,dystransthyretinemic hyperthyroxinemia,,,145680,,,
+BMGC_DS21243,BMG_DS079883,,,,,,,DOID:0050540,Charcot-Marie-Tooth disease type 3,,,145900,,,
+BMGC_DS21244,BMG_DS079884,,,,,,,DOID:0110913,adult hypophosphatasia,,,146300,,,
+BMGC_DS21245,BMG_DS079885,,,,,,,DOID:0110699,hypotrichosis 2,,,146520,,,
+BMGC_DS21246,BMG_DS079886,,,,,,,DOID:0110701,hypotrichosis 4,,,146550,,,
+BMGC_DS21247,BMG_DS079887,,,,,,,DOID:0111380,solitary median maxillary central incisor,,,147250,,,
+BMGC_DS21248,BMG_DS079888,,,,,,,DOID:0080214,punctate palmoplantar keratoderma type I,,,148600;614936,,,
+BMGC_DS21249,BMG_DS079889,,,,,,,DOID:0050658,Bart-Pumphrey syndrome,,,149200,,,
+BMGC_DS21250,BMG_DS079890,,,,,,,DOID:0050331,lacrimoauriculodentodigital syndrome 1,,,149730,,,
+BMGC_DS21251,BMG_DS079891,,,,,,,DOID:0080548,Noonan syndrome with multiple lentigines 1,,,151100,,,
+BMGC_DS21252,BMG_DS079892,,,,,,,DOID:0080081,nonsyndromic congenital nail disorder 3,,,151600,,,
+BMGC_DS21253,BMG_DS079893,,,,,,,DOID:0111503,Li-Fraumeni syndrome 1,,,151623,,,
+BMGC_DS21254,BMG_DS079894,,,,,,,DOID:0070210,hereditary lymphedema IA,,,153100,,,
+BMGC_DS21255,BMG_DS079895,,,,,,,DOID:0110015,age related macular degeneration 2,,,153800,,,
+BMGC_DS21256,BMG_DS079896,,,,,,,DOID:0080789,Treacher Collins syndrome 1,,,154500,,,
+BMGC_DS21257,BMG_DS079897,,,,,,,DOID:0080020,Jansen's metaphyseal chondrodysplasia,,,156400,,,
+BMGC_DS21258,BMG_DS079898,,,,,,,DOID:0080021,Schmid metaphyseal chondrodysplasia,,,156500,,,
+BMGC_DS21259,BMG_DS079899,,,,,,,DOID:0111521,autosomal dominant progressive external ophthalmoplegia 1,,,157640,,,
+BMGC_DS21260,BMG_DS079900,,,,,,,DOID:0111199,autosomal dominant distal hereditary motor neuronopathy 7,,,158580,,,
+BMGC_DS21261,BMG_DS079901,,,,,,,DOID:0070351,spinal muscular atrophy with lower extremity predominant 1,,,158600,,,
+BMGC_DS21262,BMG_DS079902,,,,,,,DOID:0111193,facioscapulohumeral muscular dystrophy 2,,,158901,,,
+BMGC_DS21263,BMG_DS079903,,,,,,,DOID:0050989,episodic ataxia type 1,,,160120,,,
+BMGC_DS21264,BMG_DS079904,,,,,,,DOID:0111223,centronuclear myopathy 1,,,160150,,,
+BMGC_DS21265,BMG_DS079905,,,,,,,DOID:0070197,distal myopathy 1,,,160500,,,
+BMGC_DS21266,BMG_DS079906,,,,,,,DOID:0081336,Thomsen disease,,,160800,,,
+BMGC_DS21267,BMG_DS079908,,,,,,,DOID:0080079,nonsyndromic congenital nail disorder 1,,,161050,,,
+BMGC_DS21268,BMG_DS079909,,,,,,,DOID:0110927,nemaline myopathy 3,,,161800,,,
+BMGC_DS21269,BMG_DS079910,,,,,,,DOID:0060062,familial juvenile hyperuricemic nephropathy,,,162000;613092;614227,,,
+BMGC_DS21270,BMG_DS079911,,,,,,,DOID:0070152,hereditary sensory and autonomic neuropathy type 1A,,,162400,,,
+BMGC_DS21271,BMG_DS079912,,,,,,,DOID:5806,stork bite,,,163100,,,
+BMGC_DS21272,BMG_DS079913,,,,,,,DOID:0111792,congenital nystagmus 2,,,164100,,,
+BMGC_DS21273,BMG_DS079914,,,,,,,DOID:0050954,spinocerebellar ataxia type 1,,,164400,,,
+BMGC_DS21274,BMG_DS079915,,,,,,,DOID:0050958,spinocerebellar ataxia type 7,,,164500,,,
+BMGC_DS21275,BMG_DS079916,,,,,,,DOID:0080083,nonsyndromic congenital nail disorder 5,,,164800,,,
+BMGC_DS21276,BMG_DS079918,,,,,,,DOID:0111441,optic atrophy 1,,,165500,,,
+BMGC_DS21277,BMG_DS079919,,,,,,,DOID:0111385,inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1,,,167320,,,
+BMGC_DS21278,BMG_DS079920,,,,,,,DOID:0110858,polycystic kidney disease 1,,,173900,,,
+BMGC_DS21279,BMG_DS079921,,,,,,,DOID:0060980,polycystic liver disease 1,,,174050,,,
+BMGC_DS21280,BMG_DS079922,,,,,,,DOID:0060987,preaxial polydactyly I,,,174400,,,
+BMGC_DS21281,BMG_DS079923,,,,,,,DOID:0060986,preaxial polydactyly II,,,174500,,,
+BMGC_DS21282,BMG_DS079924,,,,,,,DOID:0060985,preaxial polydactyly type IV,,,174700,,,
+BMGC_DS21283,BMG_DS079925,,,,,,,DOID:0111543,juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome,,,175050,,,
+BMGC_DS21284,BMG_DS079926,,,,,,,DOID:0080409,familial adenomatous polyposis 1,,,175100,,,
+BMGC_DS21285,BMG_DS079927,,,,,,,DOID:0090125,brain small vessel disease 1,,,175780,,,
+BMGC_DS21286,BMG_DS079928,,,,,,,DOID:0080213,punctate palmoplantar keratoderma type II,,,175860,,,
+BMGC_DS21287,BMG_DS079929,,,,,,,DOID:0070029,ITM2B-related cerebral amyloid angiopathy 1,,,176500,,,
+BMGC_DS21288,BMG_DS079930,,,,,,,DOID:0111286,psoriasis 1,,,177900,,,
+BMGC_DS21289,BMG_DS079931,,,,,,,DOID:0081321,"contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A",,,178110,,,
+BMGC_DS21290,BMG_DS079932,,,,,,,DOID:0111547,retinal arterial tortuosity,,,180000,,,
+BMGC_DS21291,BMG_DS079933,,,,,,,DOID:0070077,schizophrenia 1,,,181510,,,
+BMGC_DS21292,BMG_DS079934,,,,,,,DOID:0110916,hereditary spherocytosis type 1,,,182900,,,
+BMGC_DS21293,BMG_DS079935,,,,,,,DOID:0050956,spinocerebellar ataxia type 6,,,183086,,,
+BMGC_DS21294,BMG_DS079936,,,,,,,DOID:0050955,spinocerebellar ataxia type 2,,,183090,,,
+BMGC_DS21295,BMG_DS079937,,,,,,,DOID:0112285,autosomal dominant spondyloepiphyseal dysplasia tarda,,,184100,,,
+BMGC_DS21296,BMG_DS079938,,,,,,,DOID:0080028,"spondyloepimetaphyseal dysplasia, Strudwick type",,,184250,,,
+BMGC_DS21297,BMG_DS079939,,,,,,,DOID:0080677,"otospondylomegaepiphyseal dysplasia, autosomal dominant",,,184840,,,
+BMGC_DS21298,BMG_DS079940,,,,,,,DOID:0111562,overhydrated hereditary stomatocytosis,,,185000,,,
+BMGC_DS21299,BMG_DS079941,,,,,,,DOID:0111816,syndactyly type 1,,,185900,,,
+BMGC_DS21300,BMG_DS079942,,,,,,,DOID:0081317,multiple synostoses syndrome 1,,,186500,,,
+BMGC_DS21301,BMG_DS079943,,,,,,,DOID:0080774;DOID:0080771,beta-thalassemia major | thalassemia minor,,,187550,,,
+BMGC_DS21302,BMG_DS079944,,,,,,,DOID:0080701,prothrombin thrombophilia,,,188050,,,
+BMGC_DS21303,BMG_DS079945,,,,,,,DOID:0080171,esophageal atresia/tracheoesophageal fistula,,,189960,,,
+BMGC_DS21304,BMG_DS079946,,,,,,,DOID:0111566,familial isolated trichomegaly,,,190330,,,
+BMGC_DS21305,BMG_DS079947,,,,,,,DOID:0080376,trichorhinophalangeal syndrome type III,,,190351,,,
+BMGC_DS21306,BMG_DS079948,,,,,,,DOID:0080654,uric acid urolithiasis,,,191700,,,
+BMGC_DS21307,BMG_DS079949,,,,,,,DOID:0110307,hypertrophic cardiomyopathy 1,,,192600,,,
+BMGC_DS21308,BMG_DS079950,,,,,,,DOID:0050948,autosomal dominant hypophosphatemic rickets,,,193100,,,
+BMGC_DS21309,BMG_DS079951,,,,,,,DOID:0070483,Watson syndrome,,,193520,,,
+BMGC_DS21310,BMG_DS079952,,,,,,,DOID:0111605,distal arthrogryposis type 2A,,,193700,,,
+BMGC_DS21311,BMG_DS079953,,,,,,,DOID:0111573,autosomal dominant woolly hair,,,194300,,,
+BMGC_DS21312,BMG_DS079954,,,,,,,DOID:0050603,acheiropody,,,200500,,,
+BMGC_DS21313,BMG_DS079955,,,,,,,DOID:0080054,achondrogenesis type IA,,,200600,,,
+BMGC_DS21314,BMG_DS079956,,,,,,,DOID:0080052,"acromesomelic dysplasia, Grebe type",,,200700,,,
+BMGC_DS21315,BMG_DS079957,,,,,,,DOID:0080051,"acromesomelic dysplasia, Hunter-Thompson type",,,201250,,,
+BMGC_DS21316,BMG_DS079958,,,,,,,DOID:0070155,hereditary sensory and autonomic neuropathy type 2A,,,201300,,,
+BMGC_DS21317,BMG_DS079959,,,,,,,DOID:0080154,short chain acyl-CoA dehydrogenase deficiency,,,201470,,,
+BMGC_DS21318,BMG_DS079960,,,,,,,DOID:0080155,very long chain acyl-CoA dehydrogenase deficiency,,,201475,,,
+BMGC_DS21319,BMG_DS079961,,,,,,,DOID:0080621,glucocorticoid deficiency 1,,,202200,,,
+BMGC_DS21320,BMG_DS079962,,,,,,,DOID:0080622,peroxisome biogenesis disorder 2B,,,202370,,,
+BMGC_DS21321,BMG_DS079963,,,,,,,DOID:0080625,severe congenital neutropenia 1,,,202700,,,
+BMGC_DS21322,BMG_DS079964,,,,,,,DOID:0070094,oculocutaneous albinism type IA,,,203100,,,
+BMGC_DS21323,BMG_DS079965,,,,,,,DOID:0060539,Hermansky-Pudlak syndrome 1,,,203300,,,
+BMGC_DS21324,BMG_DS079966,,,,,,,DOID:0080626,corticosterone methyloxidase deficiency 1,,,203400,,,
+BMGC_DS21325,BMG_DS079967,,,,,,,DOID:0080628,alopecia-mental retardation syndrome 1,,,203650,,,
+BMGC_DS21326,BMG_DS079968,,,,,,,DOID:0111453,2-aminoadipic 2-oxoadipic aciduria,,,204750,,,
+BMGC_DS21327,BMG_DS079969,,,,,,,DOID:0110067,juvenile amyotrophic lateral sclerosis with dementia,,,205200,,,
+BMGC_DS21328,BMG_DS079970,,,,,,,DOID:0060066,pyridoxine-responsive sideroblastic anemia,,,206000,,,
+BMGC_DS21329,BMG_DS079971,,,,,,,DOID:0050642,hypochromic microcytic anemia,,,206100;615234,,,
+BMGC_DS21330,BMG_DS079972,,,,,,,DOID:0081290,Antley-Bixler syndrome without disordered steroidogenesis,,,207410,,,
+BMGC_DS21331,BMG_DS079973,,,,,,,DOID:0111353,"arthrogryposis, renal dysfunction, and cholestasis 1",,,208085,,,
+BMGC_DS21332,BMG_DS079974,,,,,,,DOID:0111377,fetal akinesia deformation sequence syndrome 1,,,208150,,,
+BMGC_DS21333,BMG_DS079975,,,,,,,DOID:0050649,atransferrinemia,,,209300,,,
+BMGC_DS21334,BMG_DS079976,,,,,,,DOID:0080756,atrophoderma vermiculata,,,209700,,,
+BMGC_DS21335,BMG_DS079977,,,,,,,DOID:0080631,Elsahy-Waters syndrome,,,211380,,,
+BMGC_DS21336,BMG_DS079978,,,,,,,DOID:0080632,Fazio-Londe disease,,,211500,,,
+BMGC_DS21337,BMG_DS079979,,,,,,,DOID:0080785,Brown-Vialetto-Van Laere syndrome 1,,,211530,,,
+BMGC_DS21338,BMG_DS079980,,,,,,,DOID:0111582,hereditary arterial and articular multiple calcification syndrome,,,211800,,,
+BMGC_DS21339,BMG_DS079981,,,,,,,DOID:0080552,congenital disorder of glycosylation Ia,,,212065,,,
+BMGC_DS21340,BMG_DS079982,,,,,,,DOID:0080635,optic disc anomalies with retinal and/or macular dystrophy,,,212550,,,
+BMGC_DS21341,BMG_DS079983,,,,,,,DOID:0110980,Joubert syndrome 1,,,213300,,,
+BMGC_DS21342,BMG_DS079984,,,,,,,DOID:0080911,cerebrooculofacioskeletal syndrome 1,,,214150,,,
+BMGC_DS21343,BMG_DS079985,,,,,,,DOID:0080590,Klippel-Feil syndrome 2,,,214300,,,
+BMGC_DS21344,BMG_DS079986,,,,,,,DOID:0080019,metaphyseal dysplasia,,,215050,,,
+BMGC_DS21345,BMG_DS079987,,,,,,,DOID:0070340,classic citrullinemia,,,215700,,,
+BMGC_DS21346,BMG_DS079988,,,,,,,DOID:0080907,Cockayne syndrome A,,,216400,,,
+BMGC_DS21347,BMG_DS079989,,,,,,,DOID:0060649,congenital hereditary endothelial dystrophy of cornea,,,217700,,,
+BMGC_DS21348,BMG_DS079990,,,,,,,DOID:0080802,autosomal recessive craniometaphyseal dysplasia,,,218400,,,
+BMGC_DS21349,BMG_DS079991,,,,,,,DOID:0111623,ACTH-independent macronodular adrenal hyperplasia 1,,,219080,,,
+BMGC_DS21350,BMG_DS079992,,,,,,,DOID:0111752,autosomal-mitochondrial sensorineural deafness,,,221745,,,
+BMGC_DS21351,BMG_DS079993,,,,,,,DOID:0061021,combined pituitary hormone deficiency 3,,,221750,,,
+BMGC_DS21352,BMG_DS079994,,,,,,,DOID:0111630,familial erythrocytosis 8,,,222800,,,
+BMGC_DS21353,BMG_DS079995,,,,,,,DOID:0111167,Dyggve-Melchior-Clausen disease,,,223800,,,
+BMGC_DS21354,BMG_DS079996,,,,,,,DOID:0111649,"ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome",,,225280,,,
+BMGC_DS21355,BMG_DS079997,,,,,,,DOID:0080730,Ehlers-Danlos syndrome cardiac valvular type,,,225320,,,
+BMGC_DS21356,BMG_DS079998,,,,,,,DOID:0080734,Ehlers-Danlos syndrome kyphoscoliotic type 1,,,225400,,,
+BMGC_DS21357,BMG_DS079999,,,,,,,DOID:0111095,Fanconi anemia complementation group A,,,227650,,,
+BMGC_DS21358,BMG_DS080000,,,,,,,DOID:0080109,infantile myofibromatosis,,,228550;615293,,,
+BMGC_DS21359,BMG_DS080001,,,,,,,DOID:0080502,GM1 gangliosidosis type 1,,,230500,,,
+BMGC_DS21360,BMG_DS080002,,,,,,,DOID:0080501,GM1 gangliosidosis type 2,,,230600,,,
+BMGC_DS21361,BMG_DS080003,,,,,,,DOID:0080489,GM1 gangliosidosis type 3,,,230650,,,
+BMGC_DS21362,BMG_DS080004,,,,,,,DOID:0112249,GAPO syndrome,,,230740,,,
+BMGC_DS21363,BMG_DS080005,,,,,,,DOID:0112250,Gaucher's disease type IIIC,,,231005,,,
+BMGC_DS21364,BMG_DS080006,,,,,,,DOID:0112251,Ghosal hematodiaphyseal syndrome,,,231095,,,
+BMGC_DS21365,BMG_DS080007,,,,,,,DOID:0050602,triple-A syndrome,,,231550,,,
+BMGC_DS21366,BMG_DS080008,,,,,,,DOID:0112246,glutaric acidemia type 3,,,231690,,,
+BMGC_DS21367,BMG_DS080009,,,,,,,DOID:0112252,congenital nonspherocytic hemolytic anemia 6,,,231900,,,
+BMGC_DS21368,BMG_DS080010,,,,,,,DOID:2749,glycogen storage disease Ia,,,232200,,,
+BMGC_DS21369,BMG_DS080011,,,,,,,DOID:0081330,glycogen storage disease Ib,,,232220,,,
+BMGC_DS21370,BMG_DS080012,,,,,,,DOID:0080493,ovarian dysgenesis 1,,,233300,,,
+BMGC_DS21371,BMG_DS080013,,,,,,,DOID:0050857,Perrault syndrome,,,233400;614129;614926;615300;PS233400,,,
+BMGC_DS21372,BMG_DS080014,,,,,,,DOID:0111774,"46,XY sex reversal 7",,,233420,,,
+BMGC_DS21373,BMG_DS080015,,,,,,,DOID:0070192,autosomal recessive chronic granulomatous disease 1,,,233700,,,
+BMGC_DS21374,BMG_DS080016,,,,,,,DOID:0070191,autosomal recessive chronic granulomatous disease 2,,,233710,,,
+BMGC_DS21375,BMG_DS080017,,,,,,,DOID:0112225,BH4-deficient hyperphenylalaninemia B,,,233910,,,
+BMGC_DS21376,BMG_DS080018,,,,,,,DOID:0050528,nonphotosensitive trichothiodystrophy 4,,,234050,,,
+BMGC_DS21377,BMG_DS080019,,,,,,,DOID:0110881,holoprosencephaly 1,,,236100,,,
+BMGC_DS21378,BMG_DS080020,,,,,,,DOID:0112255,homocystinuria-megaloblastic anemia cblE type,,,236270,,,
+BMGC_DS21379,BMG_DS080021,,,,,,,DOID:0080327,"multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly",,,236500,,,
+BMGC_DS21380,BMG_DS080022,,,,,,,DOID:0111237,congenital muscular dystrophy-dystroglycanopathy type A1,,,236670,,,
+BMGC_DS21381,BMG_DS080023,,,,,,,DOID:0112258,N-acetylglutamate synthase deficiency,,,237310,,,
+BMGC_DS21382,BMG_DS080024,,,,,,,DOID:0112260,Leydig cell hypoplasia type I,,,238320,,,
+BMGC_DS21383,BMG_DS080025,,,,,,,DOID:0050720,ornithine translocase deficiency,,,238970,,,
+BMGC_DS21384,BMG_DS080026,,,,,,,DOID:0081368,Paget's disease of bone 5,,,239000,,,
+BMGC_DS21385,BMG_DS080027,,,,,,,DOID:0080036,SOST-related sclerosing bone dysplasia,,,239100,,,
+BMGC_DS21386,BMG_DS080028,,,,,,,DOID:0080542,hyperprolinemia type 1,,,239500,,,
+BMGC_DS21387,BMG_DS080029,,,,,,,DOID:0050167,autoimmune polyendocrine syndrome type 1,,,240300,,,
+BMGC_DS21388,BMG_DS080030,,,,,,,DOID:0112262,leucine-sensitive hypoglycemia of infancy,,,240800,,,
+BMGC_DS21389,BMG_DS080031,,,,,,,DOID:0110914,infantile hypophosphatasia,,,241500,,,
+BMGC_DS21390,BMG_DS080032,,,,,,,DOID:0110915,childhood hypophosphatasia,,,241510,,,
+BMGC_DS21391,BMG_DS080033,,,,,,,DOID:0050949,autosomal recessive hypophosphatemic rickets,,,241520;613312,,,
+BMGC_DS21392,BMG_DS080034,,,,,,,DOID:0050655,Bamforth-Lazarus syndrome,,,241850,,,
+BMGC_DS21393,BMG_DS080035,,,,,,,DOID:0080679,neuronal intestinal dysplasia type A,,,243180,,,
+BMGC_DS21394,BMG_DS080036,,,,,,,DOID:0070231,benign recurrent intrahepatic cholestasis 1,,,243300,,,
+BMGC_DS21395,BMG_DS080037,,,,,,,DOID:0111422,familial lipase maturation factor 1 deficiency,,,246650,,,
+BMGC_DS21396,BMG_DS080038,,,,,,,DOID:0060577,3MC syndrome 3,,,248340,,,
+BMGC_DS21397,BMG_DS080039,,,,,,,DOID:0081128,mandibuloacral dysplasia type A lipodystrophy,,,248370,,,
+BMGC_DS21398,BMG_DS080040,,,,,,,DOID:0080791,Treacher Collins syndrome 3,,,248390,,,
+BMGC_DS21399,BMG_DS080041,,,,,,,DOID:0080195,Marinesco-Sjogren syndrome,,,248800,,,
+BMGC_DS21400,BMG_DS080042,,,,,,,DOID:0081177,autosomal recessive intellectual developmental disorder 1,,,249500,,,
+BMGC_DS21401,BMG_DS080043,,,,,,,DOID:0060949,3-hydroxyisobutryl-CoA hydrolase deficiency,,,250620,,,
+BMGC_DS21402,BMG_DS080044,,,,,,,DOID:0112256,homocystinuria-megaloblastic anemia cblG type,,,250940,,,
+BMGC_DS21403,BMG_DS080045,,,,,,,DOID:0070285,primary autosomal recessive microcephaly 1,,,251200,,,
+BMGC_DS21404,BMG_DS080046,,,,,,,DOID:0081432,microcephaly-micromelia syndrome,,,251230,,,
+BMGC_DS21405,BMG_DS080047,,,,,,,DOID:0060959,orofaciodigital syndrome II,,,252100,,,
+BMGC_DS21406,BMG_DS080048,,,,,,,DOID:0080070,mucolipidosis II alpha/beta,,,252500,,,
+BMGC_DS21407,BMG_DS080049,,,,,,,DOID:0080071,mucolipidosis III alpha/beta,,,252600,,,
+BMGC_DS21408,BMG_DS080050,,,,,,,DOID:0080490,mucolipidosis type IV,,,252650,,,
+BMGC_DS21409,BMG_DS080051,,,,,,,DOID:0050559,Fukuyama congenital muscular dystrophy,,,253800,,,
+BMGC_DS21410,BMG_DS080052,,,,,,,DOID:0070199,Miyoshi muscular dystrophy 1,,,254130,,,
+BMGC_DS21411,BMG_DS080053,,,,,,,DOID:0110671,congenital myasthenic syndrome 6,,,254210,,,
+BMGC_DS21412,BMG_DS080054,,,,,,,DOID:0110668,congenital myasthenic syndrome 10,,,254300,,,
+BMGC_DS21413,BMG_DS080055,,,,,,,DOID:0111452,progressive myoclonus epilepsy 1A,,,254800,,,
+BMGC_DS21414,BMG_DS080056,,,,,,,DOID:0111268,autosomal recessive hyaline body myopathy,,,255160,,,
+BMGC_DS21415,BMG_DS080057,,,,,,,DOID:0081335,Becker disease,,,255300;255700,,,
+BMGC_DS21416,BMG_DS080058,,,,,,,DOID:0080102,congenital myopathy 4A,,,255310,,,
+BMGC_DS21417,BMG_DS080059,,,,,,,DOID:0080991,congenital myopathy 1B,,,255320,,,
+BMGC_DS21418,BMG_DS080060,,,,,,,DOID:0111112,nephronophthisis 1,,,256100,,,
+BMGC_DS21419,BMG_DS080061,,,,,,,DOID:0070219,familial hyperinsulinemic hypoglycemia 1,,,256450,,,
+BMGC_DS21420,BMG_DS080062,,,,,,,DOID:0070160,atypical hereditary sensory neuropathy,,,256860,,,
+BMGC_DS21421,BMG_DS080063,,,,,,,DOID:0080141,mosaic variegated aneuploidy syndrome 1,,,257300,,,
+BMGC_DS21422,BMG_DS080064,,,,,,,DOID:0080849,"ocular motor apraxia, Cogan type",,,257550,,,
+BMGC_DS21423,BMG_DS080065,,,,,,,DOID:0060575,3MC syndrome 1,,,257920,,,
+BMGC_DS21424,BMG_DS080066,,,,,,,DOID:0080175;DOID:0080173,bladder exstrophy-epispadias-cloacal exstrophy complex | cloacal exstrophy,,,258040,,,
+BMGC_DS21425,BMG_DS080067,,,,,,,DOID:0110712,Oguchi disease-1,,,258100,,,
+BMGC_DS21426,BMG_DS080068,,,,,,,DOID:0070188,spermatogenic failure 1,,,258150,,,
+BMGC_DS21427,BMG_DS080069,,,,,,,DOID:0110004,3-methylglutaconic aciduria type 3,,,258501,,,
+BMGC_DS21428,BMG_DS080070,,,,,,,DOID:0110942,autosomal recessive osteopetrosis 1,,,259700,,,
+BMGC_DS21429,BMG_DS080071,,,,,,,DOID:0110943,autosomal recessive osteopetrosis 2,,,259710,,,
+BMGC_DS21430,BMG_DS080072,,,,,,,DOID:0110939,autosomal recessive osteopetrosis 5,,,259720,,,
+BMGC_DS21431,BMG_DS080073,,,,,,,DOID:0060372,Parkinson's disease 15,,,260300,,,
+BMGC_DS21432,BMG_DS080074,,,,,,,DOID:0081450,hyperimmunoglobulinemia D periodic fever syndrome,,,260920,,,
+BMGC_DS21433,BMG_DS080075,,,,,,,DOID:0050734,congenital intrinsic factor deficiency,,,261000,,,
+BMGC_DS21434,BMG_DS080076,,,,,,,DOID:0080201,Peters plus syndrome,,,261540,,,
+BMGC_DS21435,BMG_DS080077,,,,,,,DOID:0081130,BH4-deficient hyperphenylalaninemia C,,,261630,,,
+BMGC_DS21436,BMG_DS080078,,,,,,,DOID:0061020,combined pituitary hormone deficiency 2,,,262600,,,
+BMGC_DS21437,BMG_DS080079,,,,,,,DOID:0080212,polycystic kidney disease 4,,,263200,,,
+BMGC_DS21438,BMG_DS080080,,,,,,,DOID:0081131,BH4-deficient hyperphenylalaninemia D,,,264070,,,
+BMGC_DS21439,BMG_DS080081,,,,,,,DOID:0081333,Wiedemann-Rautenstrauch syndrome,,,264090,,,
+BMGC_DS21440,BMG_DS080082,,,,,,,DOID:0080886,vitamin D-dependent rickets type 1A,,,264700,,,
+BMGC_DS21441,BMG_DS080083,,,,,,,DOID:0060576,3MC syndrome 2,,,265050,,,
+BMGC_DS21442,BMG_DS080084,,,,,,,DOID:0051007,congenital nonspherocytic hemolytic anemia 8,,,266120,,,
+BMGC_DS21443,BMG_DS080085,,,,,,,DOID:0081034,glutatione synthetase deficiency with 5-oxoprolinuria,,,266130,,,
+BMGC_DS21444,BMG_DS080086,,,,,,,DOID:0110892,inflammatory bowel disease 1,,,266600,,,
+BMGC_DS21445,BMG_DS080087,,,,,,,DOID:0110921,familial hemophagocytic lymphohistiocytosis 1,,,267700,,,
+BMGC_DS21446,BMG_DS080088,,,,,,,DOID:0070026,Revesz syndrome,,,268130,,,
+BMGC_DS21447,BMG_DS080089,,,,,,,DOID:0050168,autoimmune polyendocrine syndrome type 2,,,269200,,,
+BMGC_DS21448,BMG_DS080090,,,,,,,DOID:0070176,spermatogenic failure 4,,,270960,,,
+BMGC_DS21449,BMG_DS080091,,,,,,,DOID:0110918,hereditary spherocytosis type 3,,,270970,,,
+BMGC_DS21450,BMG_DS080092,,,,,,,DOID:0112293,autosomal recessive spondyloepiphyseal dysplasia tarda,,,271600,,,
+BMGC_DS21451,BMG_DS080093,,,,,,,DOID:0112195,spondyloperipheral dysplasia,,,271700,,,
+BMGC_DS21452,BMG_DS080094,,,,,,,DOID:0110979,Sugarman brachydactyly,,,272150,,,
+BMGC_DS21453,BMG_DS080095,,,,,,,DOID:0080329,cold-induced sweating syndrome 1,,,272430,,,
+BMGC_DS21454,BMG_DS080096,,,,,,,DOID:0050818,transcobalamin II deficiency,,,275350,,,
+BMGC_DS21455,BMG_DS080097,,,,,,,DOID:0050729,Chanarin-Dorfman syndrome,,,275630,,,
+BMGC_DS21456,BMG_DS080098,,,,,,,DOID:0112182,mismatch repair cancer syndrome,,,276300,,,
+BMGC_DS21457,BMG_DS080099,,,,,,,DOID:0050725,tyrosinemia type II,,,276600,,,
+BMGC_DS21458,BMG_DS080100,,,,,,,DOID:0050726,tyrosinemia type I,,,276700,,,
+BMGC_DS21459,BMG_DS080101,,,,,,,DOID:0050727,tyrosinemia type III,,,276710,,,
+BMGC_DS21460,BMG_DS080102,,,,,,,DOID:0112181,Schinzel type phocomelia,,,276820,,,
+BMGC_DS21461,BMG_DS080103,,,,,,,DOID:0112178,Mayer-Rokitansky-Kuster-Hauser syndrome type 1,,,277000,,,
+BMGC_DS21462,BMG_DS080104,,,,,,,DOID:0111864,autosomal recessive congenital bilateral absence of vas deferens,,,277180,,,
+BMGC_DS21463,BMG_DS080105,,,,,,,DOID:0112365,spondylocostal dysostosis 1,,,277300,,,
+BMGC_DS21464,BMG_DS080106,,,,,,,DOID:0050717,methylmalonic aciduria and homocystinuria type cblF,,,277380,,,
+BMGC_DS21465,BMG_DS080107,,,,,,,DOID:0050716,methylmalonic aciduria and homocystinuria type cblD,,,277410,,,
+BMGC_DS21466,BMG_DS080108,,,,,,,DOID:0080884,vitamin D-dependent rickets type 2A,,,277440,,,
+BMGC_DS21467,BMG_DS080109,,,,,,,DOID:0111606,autosomal recessive Whistling face syndrome,,,277720,,,
+BMGC_DS21468,BMG_DS080110,,,,,,,DOID:0080697,Opitz GBBB syndrome,,,300000,,,
+BMGC_DS21469,BMG_DS080111,,,,,,,DOID:0112151,corpus callosum agenesis-abnormal genitalia syndrome,,,300004,,,
+BMGC_DS21470,BMG_DS080112,,,,,,,DOID:0111736,X-linked deafness 3,,,300030,,,
+BMGC_DS21471,BMG_DS080113,,,,,,,DOID:0112049,non-syndromic X-linked intellectual disability 23,,,300046,,,
+BMGC_DS21472,BMG_DS080114,,,,,,,DOID:0112023,non-syndromic X-linked intellectual disability 20,,,300047,,,
+BMGC_DS21473,BMG_DS080115,,,,,,,DOID:0112027,non-syndromic X-linked intellectual disability 14,,,300062,,,
+BMGC_DS21474,BMG_DS080116,,,,,,,DOID:0111735,X-linked deafness 4,,,300066,,,
+BMGC_DS21475,BMG_DS080117,,,,,,,DOID:0081043,fetal akinesia deformation sequence syndrome X-linked,,,300073,,,
+BMGC_DS21476,BMG_DS080118,,,,,,,DOID:0080156,X-linked adrenal hypoplasia congenita,,,300200,,,
+BMGC_DS21477,BMG_DS080119,,,,,,,DOID:0080342,Simpson-Golabi-Behmel syndrome type 2,,,300209,,,
+BMGC_DS21478,BMG_DS080120,,,,,,,DOID:0112238,X-linked lissencephaly 2,,,300215,,,
+BMGC_DS21479,BMG_DS080121,,,,,,,DOID:0112059,non-syndromic X-linked intellectual disability 72,,,300271,,,
+BMGC_DS21480,BMG_DS080122,,,,,,,DOID:0081078,ectodermal dysplasia and immunodeficiency 1,,,300291,,,
+BMGC_DS21481,BMG_DS080123,,,,,,,DOID:0112127,HRPT-related hyperuricemia,,,300323,,,
+BMGC_DS21482,BMG_DS080124,,,,,,,DOID:0112047,non-syndromic X-linked intellectual disability 53,,,300324,,,
+BMGC_DS21483,BMG_DS080125,,,,,,,DOID:0050800,cerebral creatine deficiency syndrome 1,,,300352,,,
+BMGC_DS21484,BMG_DS080126,,,,,,,DOID:0112017,non-syndromic X-linked intellectual disability 73,,,300355,,,
+BMGC_DS21485,BMG_DS080127,,,,,,,DOID:0112057,non-syndromic X-linked intellectual disability 42,,,300372,,,
+BMGC_DS21486,BMG_DS080128,,,,,,,DOID:0112050,non-syndromic X-linked intellectual disability 63,,,300387,,,
+BMGC_DS21487,BMG_DS080129,,,,,,,DOID:0112016,non-syndromic X-linked intellectual disability 2,,,300428,,,
+BMGC_DS21488,BMG_DS080130,,,,,,,DOID:0112033,non-syndromic X-linked intellectual disability 81,,,300433,,,
+BMGC_DS21489,BMG_DS080131,,,,,,,DOID:0112126,Stocco Dos Santos type X-linked intellectual disability,,,300434,,,
+BMGC_DS21490,BMG_DS080132,,,,,,,DOID:0112055,non-syndromic X-linked intellectual disability 46,,,300436,,,
+BMGC_DS21491,BMG_DS080133,,,,,,,DOID:0112039,non-syndromic X-linked intellectual disability 77,,,300454,,,
+BMGC_DS21492,BMG_DS080134,,,,,,,DOID:0112124,X-linked retinitis pigmentosa and sinorespiratory infections,,,300455,,,
+BMGC_DS21493,BMG_DS080135,,,,,,,DOID:0080311,X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance,,,300486,,,
+BMGC_DS21494,BMG_DS080136,,,,,,,DOID:0112028,non-syndromic X-linked intellectual disability 45,,,300498,,,
+BMGC_DS21495,BMG_DS080137,,,,,,,DOID:0112030,non-syndromic X-linked intellectual disability 84,,,300505,,,
+BMGC_DS21496,BMG_DS080138,,,,,,,DOID:0080861,primary ovarian insufficiency 4,,,300510,,,
+BMGC_DS21497,BMG_DS080139,,,,,,,DOID:0080858,primary ovarian insufficiency 2A,,,300511,,,
+BMGC_DS21498,BMG_DS080140,,,,,,,DOID:0112052,non-syndromic X-linked intellectual disability 82,,,300518,,,
+BMGC_DS21499,BMG_DS080141,,,,,,,DOID:0080353,X-linked recessive hypophosphatemic rickets,,,300554,,,
+BMGC_DS21500,BMG_DS080142,,,,,,,DOID:0112043,non-syndromic X-linked intellectual disability 91,,,300577,,,
+BMGC_DS21501,BMG_DS080143,,,,,,,DOID:0111226,X-linked congenital myopathy with fiber-type disproportion,,,300580,,,
+BMGC_DS21502,BMG_DS080144,,,,,,,DOID:0112120,SHOX-related short stature,,,300582,,,
+BMGC_DS21503,BMG_DS080145,,,,,,,DOID:0111796,congenital nystagmus 5,,,300589,,,
+BMGC_DS21504,BMG_DS080146,,,,,,,DOID:0080506,Cornelia de Lange syndrome 2,,,300590,,,
+BMGC_DS21505,BMG_DS080147,,,,,,,DOID:0080859,primary ovarian insufficiency 2B,,,300604,,,
+BMGC_DS21506,BMG_DS080148,,,,,,,DOID:0080215,developmental and epileptic encephalopathy 8,,,300607,,,
+BMGC_DS21507,BMG_DS080149,,,,,,,DOID:0111741,X-linked deafness 5,,,300614,,,
+BMGC_DS21508,BMG_DS080150,,,,,,,DOID:0080520,Tn polyagglutination syndrome,,,300622,,,
+BMGC_DS21509,BMG_DS080151,,,,,,,DOID:0080467,developmental and epileptic encephalopathy 2,,,300672,,,
+BMGC_DS21510,BMG_DS080152,,,,,,,DOID:0070251,X-linked Emery-Dreifuss muscular dystrophy 6,,,300696,,,
+BMGC_DS21511,BMG_DS080153,,,,,,,DOID:0050776,non-syndromic X-linked intellectual disability,,,300716;PS309530,,,
+BMGC_DS21512,BMG_DS080154,,,,,,,DOID:0060063,sideroblastic anemia 1,,,300751,,,
+BMGC_DS21513,BMG_DS080155,,,,,,,DOID:0110036,Alzheimer's disease 16,,,300756,,,
+BMGC_DS21514,BMG_DS080156,,,,,,,DOID:0112046,non-syndromic X-linked intellectual disability 97,,,300803,,,
+BMGC_DS21515,BMG_DS080157,,,,,,,DOID:0112031,non-syndromic X-linked intellectual disability 89,,,300848,,,
+BMGC_DS21516,BMG_DS080158,,,,,,,DOID:0112041,non-syndromic X-linked intellectual disability 90,,,300850,,,
+BMGC_DS21517,BMG_DS080159,,,,,,,DOID:0112032,non-syndromic X-linked intellectual disability 92,,,300851,,,
+BMGC_DS21518,BMG_DS080160,,,,,,,DOID:0080319,"X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia",,,300853,,,
+BMGC_DS21519,BMG_DS080161,,,,,,,DOID:0050781,Ogden syndrome,,,300855,,,
+BMGC_DS21520,BMG_DS080162,,,,,,,DOID:0060803,syndromic X-linked intellectual disability 17,,,300858,,,
+BMGC_DS21521,BMG_DS080163,,,,,,,DOID:0060819,syndromic X-linked intellectual disability Chudley-Schwartz type,,,300861,,,
+BMGC_DS21522,BMG_DS080164,,,,,,,DOID:0080968,intracranial berry aneurysm 5,,,300870,,,
+BMGC_DS21523,BMG_DS080165,,,,,,,DOID:0080470,developmental and epileptic encephalopathy 36,,,300884,,,
+BMGC_DS21524,BMG_DS080166,,,,,,,DOID:0070265,congenital disorder of glycosylation type IIm,,,300896,,,
+BMGC_DS21525,BMG_DS080167,,,,,,,DOID:0112026,non-syndromic X-linked intellectual disability 99,,,300919,,,
+BMGC_DS21526,BMG_DS080168,,,,,,,DOID:0080574,congenital disorder of glycosylation Iy,,,300934,,,
+BMGC_DS21527,BMG_DS080169,,,,,,,DOID:0112007,growth hormone secreting pituitary adenoma 2,,,300943,,,
+BMGC_DS21528,BMG_DS080170,,,,,,,DOID:0060817,syndromic X-linked intellectual disability 34,,,300967,,,
+BMGC_DS21529,BMG_DS080171,,,,,,,DOID:0112001,immunodeficiency 50,,,300988,,,
+BMGC_DS21530,BMG_DS080172,,,,,,,DOID:0080240,non-syndromic X-linked intellectual disability 106,,,300997,,,
+BMGC_DS21531,BMG_DS080173,,,,,,,DOID:0080242,syndromic X-linked mental retardation Hough type,,,301008,,,
+BMGC_DS21532,BMG_DS080174,,,,,,,DOID:0112054,non-syndromic X-linked intellectual disability 107,,,301013,,,
+BMGC_DS21533,BMG_DS080175,,,,,,,DOID:0111847,osteogenesis imperfecta type 19,,,301014,,,
+BMGC_DS21534,BMG_DS080176,,,,,,,DOID:0111840,Van Esch-O'Driscoll syndrome,,,301030,,,
+BMGC_DS21535,BMG_DS080177,,,,,,,DOID:0080839,X-linked warfarin sensitivity,,,301052,,,
+BMGC_DS21536,BMG_DS080178,,,,,,,DOID:0080828,VEXAS syndrome,,,301054,,,
+BMGC_DS21537,BMG_DS080179,,,,,,,DOID:0070422,syndromic X-linked intellectual disability Pilorge type,,,301076,,,
+BMGC_DS21538,BMG_DS080180,,,,,,,DOID:0051008,congenital nonspherocytic hemolytic anemia 9,,,301083,,,
+BMGC_DS21539,BMG_DS080181,,,,,,,DOID:0060929,non-syndromic X-linked intellectual developmental disorder 111,,,301107,,,
+BMGC_DS21540,BMG_DS080182,,,,,,,DOID:0080074,neural tube defect,,,301410;601634,,,
+BMGC_DS21541,BMG_DS080183,,,,,,,DOID:0080352,X-linked chondrodysplasia punctata 2,,,302960,,,
+BMGC_DS21542,BMG_DS080184,,,,,,,DOID:0060613,X-linked cleft palate with or without ankyloglossia,,,303400,,,
+BMGC_DS21543,BMG_DS080185,,,,,,,DOID:0111737,X-linked deafness 2,,,304400,,,
+BMGC_DS21544,BMG_DS080186,,,,,,,DOID:0111739,X-linked deafness 1,,,304500,,,
+BMGC_DS21545,BMG_DS080187,,,,,,,DOID:0081060,X-linked nephrogenic diabetes insipidus,,,304800,,,
+BMGC_DS21546,BMG_DS080188,,,,,,,DOID:0111413,X-linked exudative vitreoretinopathy 2,,,305390,,,
+BMGC_DS21547,BMG_DS080189,,,,,,,DOID:0111786,frontometaphyseal dysplasia 1,,,305620,,,
+BMGC_DS21548,BMG_DS080190,,,,,,,DOID:0070189,X-linked spermatogenic failure 1,,,305700,,,
+BMGC_DS21549,BMG_DS080191,,,,,,,DOID:0070195,X-linked chronic granulomatous disease,,,306400,,,
+BMGC_DS21550,BMG_DS080192,,,,,,,DOID:0050545,visceral heterotaxy,,,306955;605376;606325;613751;614779;PS306955,,,
+BMGC_DS21551,BMG_DS080193,,,,,,,DOID:0111388,X-linked hypoparathyroidism,,,307700,,,
+BMGC_DS21552,BMG_DS080194,,,,,,,DOID:0060022,CD40 ligand deficiency,,,308230,,,
+BMGC_DS21553,BMG_DS080195,,,,,,,DOID:0080754,X-linked keratosis follicularis spinulosa decalvans,,,308800,,,
+BMGC_DS21554,BMG_DS080196,,,,,,,DOID:0111815,low molecular weight proteinuria with hypercalciuric nephrocalcinosis,,,308990,,,
+BMGC_DS21555,BMG_DS080197,,,,,,,DOID:0080985,syndromic X-linked intellectual disorder Lujan-Fryns-type,,,309520,,,
+BMGC_DS21556,BMG_DS080198,,,,,,,DOID:0080984,X-linked intellectual developmental disorder 109,,,309548,,,
+BMGC_DS21557,BMG_DS080199,,,,,,,DOID:0112034,non-syndromic X-linked intellectual disability 9,,,309549,,,
+BMGC_DS21558,BMG_DS080200,,,,,,,DOID:0081123,X-linked mental retardation Gustavson type,,,309555,,,
+BMGC_DS21559,BMG_DS080201,,,,,,,DOID:0060805,Prieto syndrome,,,309610,,,
+BMGC_DS21560,BMG_DS080202,,,,,,,DOID:0070246,X-linked Emery-Dreifuss muscular dystrophy 1,,,310300,,,
+BMGC_DS21561,BMG_DS080203,,,,,,,DOID:0050760,X-linked myopathy with excessive autophagy,,,310440,,,
+BMGC_DS21562,BMG_DS080204,,,,,,,DOID:0111798,X-linked nephrolithiasis type I,,,310468,,,
+BMGC_DS21563,BMG_DS080205,,,,,,,DOID:0070159,hereditary sensory neuropathy X-linked,,,310470,,,
+BMGC_DS21564,BMG_DS080206,,,,,,,DOID:0110870,congenital stationary night blindness 1A,,,310500,,,
+BMGC_DS21565,BMG_DS080207,,,,,,,DOID:0111790,congenital nystagmus 1,,,310700,,,
+BMGC_DS21566,BMG_DS080208,,,,,,,DOID:0111443,optic atrophy 2,,,311050,,,
+BMGC_DS21567,BMG_DS080209,,,,,,,DOID:0080857,primary ovarian insufficiency 1,,,311360,,,
+BMGC_DS21568,BMG_DS080210,,,,,,,DOID:0111781,Waisman syndrome,,,311510,,,
+BMGC_DS21569,BMG_DS080211,,,,,,,DOID:0111779,X-linked panhypopituitarism,,,312000,,,
+BMGC_DS21570,BMG_DS080212,,,,,,,DOID:0080776,partial androgen insensitivity syndrome,,,312300,,,
+BMGC_DS21571,BMG_DS080213,,,,,,,DOID:0080362,X-linked spondyloepiphyseal dysplasia tarda,,,313400,,,
+BMGC_DS21572,BMG_DS080214,,,,,,,DOID:0070186,Y-linked spermatogenic failure 1,,,400042,,,
+BMGC_DS21573,BMG_DS080215,,,,,,,DOID:0111778,"46,XY sex reversal 1",,,400044,,,
+BMGC_DS21574,BMG_DS080216,,,,,,,DOID:0111761,"46,XX sex reversal 1",,,400045,,,
+BMGC_DS21575,BMG_DS080217,,,,,,,DOID:0080198,infantile histiocytoid cardiomyopathy,,,500000,,,
+BMGC_DS21576,BMG_DS080218,,,,,,,DOID:0060067,Pearson syndrome,,,557000,,,
+BMGC_DS21577,BMG_DS080219,,,,,,,DOID:0111733,pancreatic hypoplasia-diabetes-congenital heart disease syndrome,,,600001,,,
+BMGC_DS21578,BMG_DS080220,,,,,,,DOID:0060761,familial chronic myelocytic leukemia-like syndrome,,,600080,,,
+BMGC_DS21579,BMG_DS080221,,,,,,,DOID:0080887,vitamin D-dependent rickets type 1B,,,600081,,,
+BMGC_DS21580,BMG_DS080222,,,,,,,DOID:0080634,nanophthalmos,,,600165;609549;611897;615972;PS600165,,,
+BMGC_DS21581,BMG_DS080223,,,,,,,DOID:0111215,autosomal dominant distal hereditary motor neuronopathy 8,,,600175,,,
+BMGC_DS21582,BMG_DS080224,,,,,,,DOID:0070298,multiple epiphyseal dysplasia 2,,,600204,,,
+BMGC_DS21583,BMG_DS080225,,,,,,,DOID:0050882,spinocerebellar ataxia type 5,,,600224,,,
+BMGC_DS21584,BMG_DS080226,,,,,,,DOID:0111706,oblique facial clefting 1,,,600251,,,
+BMGC_DS21585,BMG_DS080227,,,,,,,DOID:0070343,CSF1R-related brain malformation and osteopetrosis,,,600329,,,
+BMGC_DS21586,BMG_DS080228,,,,,,,DOID:0080067,Charcot-Marie-Tooth disease type 5,,,600361,,,
+BMGC_DS21587,BMG_DS080229,,,,,,,DOID:0111102,maturity-onset diabetes of the young type 3,,,600496,,,
+BMGC_DS21588,BMG_DS080230,,,,,,,DOID:0070079,schizophrenia 3,,,600511,,,
+BMGC_DS21589,BMG_DS080231,,,,,,,DOID:0060748,familial temporal lobe epilepsy 1,,,600512,,,
+BMGC_DS21590,BMG_DS080232,,,,,,,DOID:0060682,autosomal dominant nocturnal frontal lobe epilepsy 1,,,600513,,,
+BMGC_DS21591,BMG_DS080233,,,,,,,DOID:0080885,vitamin D-dependent rickets type 2B,,,600785,,,
+BMGC_DS21592,BMG_DS080234,,,,,,,DOID:0060008,janus kinase-3 deficiency,,,600802,,,
+BMGC_DS21593,BMG_DS080235,,,,,,,DOID:0110312,hypertrophic cardiomyopathy 6,,,600858,,,
+BMGC_DS21594,BMG_DS080236,,,,,,,DOID:0080055,achondrogenesis type IB,,,600972,,,
+BMGC_DS21595,BMG_DS080237,,,,,,,DOID:0112179,Mayer-Rokitansky-Kuster-Hauser syndrome type 2,,,601076,,,
+BMGC_DS21596,BMG_DS080238,,,,,,,DOID:0080068,Charcot-Marie-Tooth disease type 6,,,601152;616505,,,
+BMGC_DS21597,BMG_DS080239,,,,,,,DOID:0081063,DICER1 syndrome,,,601200,,,
+BMGC_DS21598,BMG_DS080240,,,,,,,DOID:0080680,neuronal intestinal dysplasia type B,,,601223,,,
+BMGC_DS21599,BMG_DS080241,,,,,,,DOID:0111682,diffuse cystic renal dysplasia,,,601331,,,
+BMGC_DS21600,BMG_DS080242,,,,,,,DOID:0081441,Nicolaides-Baraitser syndrome,,,601358,,,
+BMGC_DS21601,BMG_DS080243,,,,,,,DOID:0111283,psoriasis 3,,,601454,,,
+BMGC_DS21602,BMG_DS080244,,,,,,,DOID:0050809,mucopolysaccharidosis IX,,,601492,,,
+BMGC_DS21603,BMG_DS080245,,,,,,,DOID:0050682,Athabaskan brainstem dysgenesis syndrome,,,601536,,,
+BMGC_DS21604,BMG_DS080246,,,,,,,DOID:0081240,peroxisome biogenesis disorder 1B,,,601539,,,
+BMGC_DS21605,BMG_DS080247,,,,,,,DOID:0111873,photosensitive trichothiodystrophy 1,,,601675,,,
+BMGC_DS21606,BMG_DS080248,,,,,,,DOID:0081114,benign familial infantile seizures 1,,,601764,,,
+BMGC_DS21607,BMG_DS080249,,,,,,,DOID:0080736,Ehlers-Danlos syndrome musculocontractural type 1,,,601776,,,
+BMGC_DS21608,BMG_DS080250,,,,,,,DOID:0111011,cone-rod dystrophy 6,,,601777,,,
+BMGC_DS21609,BMG_DS080251,,,,,,,DOID:0070218,familial hyperinsulinemic hypoglycemia 2,,,601820,,,
+BMGC_DS21610,BMG_DS080252,,,,,,,DOID:0111658,ectodermal dysplasia 4,,,602032,,,
+BMGC_DS21611,BMG_DS080253,,,,,,,DOID:0111275,speech-language disorder-1,,,602081,,,
+BMGC_DS21612,BMG_DS080254,,,,,,,DOID:0060197,amyotrophic lateral sclerosis type 5,,,602099,,,
+BMGC_DS21613,BMG_DS080255,,,,,,,DOID:0081362,Pierpont syndrome,,,602342,,,
+BMGC_DS21614,BMG_DS080256,,,,,,,DOID:0111250,Parkinson's disease 3,,,602404,,,
+BMGC_DS21615,BMG_DS080257,,,,,,,DOID:0070216,familial hyperinsulinemic hypoglycemia 3,,,602485,,,
+BMGC_DS21616,BMG_DS080258,,,,,,,DOID:0080554,congenital disorder of glycosylation Ib,,,602579,,,
+BMGC_DS21617,BMG_DS080259,,,,,,,DOID:0112294,"spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability",,,602611,,,
+BMGC_DS21618,BMG_DS080260,,,,,,,DOID:0111278,histiocytosis-lymphadenopathy plus syndrome,,,602782,,,
+BMGC_DS21619,BMG_DS080261,,,,,,,DOID:0110667,congenital myasthenic syndrome 5,,,603034,,,
+BMGC_DS21620,BMG_DS080262,,,,,,,DOID:0110014,age related macular degeneration 1,,,603075,,,
+BMGC_DS21621,BMG_DS080263,,,,,,,DOID:0080555,congenital disorder of glycosylation Ic,,,603147,,,
+BMGC_DS21622,BMG_DS080264,,,,,,,DOID:0070081,schizophrenia 5,,,603175,,,
+BMGC_DS21623,BMG_DS080265,,,,,,,DOID:0070083,schizophrenia 7,,,603176,,,
+BMGC_DS21624,BMG_DS080266,,,,,,,DOID:0060683,autosomal dominant nocturnal frontal lobe epilepsy 2,,,603204,,,
+BMGC_DS21625,BMG_DS080267,,,,,,,DOID:0070084,schizophrenia 8,,,603206,,,
+BMGC_DS21626,BMG_DS080268,,,,,,,DOID:0081102,familial gestational hyperthyroidism,,,603373,,,
+BMGC_DS21627,BMG_DS080269,,,,,,,DOID:0070342,adult-onset type II citrullinemia,,,603471,,,
+BMGC_DS21628,BMG_DS080270,,,,,,,DOID:0081294,neuronal intranuclear inclusion disease,,,603472,,,
+BMGC_DS21629,BMG_DS080271,,,,,,,DOID:0050960,spinocerebellar ataxia type 10,,,603516,,,
+BMGC_DS21630,BMG_DS080272,,,,,,,DOID:0060646,congenital chylothorax,,,603523,,,
+BMGC_DS21631,BMG_DS080273,,,,,,,DOID:0112199,spondyloepimetaphyseal dysplasia with joint laxity type 2,,,603546,,,
+BMGC_DS21632,BMG_DS080274,,,,,,,DOID:0110924,familial hemophagocytic lymphohistiocytosis 4,,,603552,,,
+BMGC_DS21633,BMG_DS080275,,,,,,,DOID:0111188,myofibrillar myopathy 9,,,603689,,,
+BMGC_DS21634,BMG_DS080276,,,,,,,DOID:0080770,autosomal dominant beta thalassemia,,,603902,,,
+BMGC_DS21635,BMG_DS080277,,,,,,,DOID:0081445,sickle cell disease,,,603903,,,
+BMGC_DS21636,BMG_DS080278,,,,,,,DOID:0111280,psoriasis 4,,,603935,,,
+BMGC_DS21637,BMG_DS080279,,,,,,,DOID:0080751,keratosis pilaris atrophicans,,,604093,,,
+BMGC_DS21638,BMG_DS080280,,,,,,,DOID:0060480,left ventricular noncompaction,,,604169,,,
+BMGC_DS21639,BMG_DS080281,,,,,,,DOID:0050711,aceruloplasminemia,,,604290,,,
+BMGC_DS21640,BMG_DS080282,,,,,,,DOID:0111282,psoriasis 5,,,604316,,,
+BMGC_DS21641,BMG_DS080283,,,,,,,DOID:0050962,spinocerebellar ataxia type 12,,,604326,,,
+BMGC_DS21642,BMG_DS080284,,,,,,,DOID:0111305,familial febrile seizures 4,,,604352,,,
+BMGC_DS21643,BMG_DS080285,,,,,,,DOID:0081384,ataxia-telangiectasia-like disorder-1,,,604391,,,
+BMGC_DS21644,BMG_DS080286,,,,,,,DOID:0080519,PAPA syndrome,,,604416,,,
+BMGC_DS21645,BMG_DS080287,,,,,,,DOID:4279,infundibulocystic basal cell carcinoma,,,604451,,,
+BMGC_DS21646,BMG_DS080288,,,,,,,DOID:0060009,MHC class I deficiency,,,604571,,,
+BMGC_DS21647,BMG_DS080289,,,,,,,DOID:0061009,craniosynostosis 2,,,604757,,,
+BMGC_DS21648,BMG_DS080290,,,,,,,DOID:0070286,primary autosomal recessive microcephaly 3,,,604804,,,
+BMGC_DS21649,BMG_DS080291,,,,,,,DOID:0080675,Stickler syndrome 2,,,604841,,,
+BMGC_DS21650,BMG_DS080292,,,,,,,DOID:0070085,schizophrenia 9,,,604906,,,
+BMGC_DS21651,BMG_DS080293,,,,,,,DOID:0111061,familial hypobetalipoproteinemia 2,,,605019,,,
+BMGC_DS21652,BMG_DS080294,,,,,,,DOID:0050963,spinocerebellar ataxia type 13,,,605259,,,
+BMGC_DS21653,BMG_DS080295,,,,,,,DOID:0050964,spinocerebellar ataxia type 14,,,605361,,,
+BMGC_DS21654,BMG_DS080296,,,,,,,DOID:0110440,dilated cardiomyopathy 1J,,,605362,,,
+BMGC_DS21655,BMG_DS080297,,,,,,,DOID:0111290,psoriasis 6,,,605364,,,
+BMGC_DS21656,BMG_DS080298,,,,,,,DOID:0060684,autosomal dominant nocturnal frontal lobe epilepsy 3,,,605375,,,
+BMGC_DS21657,BMG_DS080299,,,,,,,DOID:0050670,ataxic cerebral palsy,,,605388,,,
+BMGC_DS21658,BMG_DS080300,,,,,,,DOID:0070086,schizophrenia 10,,,605419,,,
+BMGC_DS21659,BMG_DS080301,,,,,,,DOID:0111279,psoriasis 7,,,605606,,,
+BMGC_DS21660,BMG_DS080302,,,,,,,DOID:0080719,congenital myopathy 6,,,605637,,,
+BMGC_DS21661,BMG_DS080303,,,,,,,DOID:0080133,multiple mitochondrial dysfunctions syndrome 1,,,605711,,,
+BMGC_DS21662,BMG_DS080304,,,,,,,DOID:0111058,platelet-type bleeding disorder 12,,,605735,,,
+BMGC_DS21663,BMG_DS080305,,,,,,,DOID:0110098,atopic dermatitis 2,,,605803,,,
+BMGC_DS21664,BMG_DS080306,,,,,,,DOID:0110099,atopic dermatitis 3,,,605804,,,
+BMGC_DS21665,BMG_DS080307,,,,,,,DOID:0110101,atopic dermatitis 5,,,605844,,,
+BMGC_DS21666,BMG_DS080308,,,,,,,DOID:0110102,atopic dermatitis 6,,,605845,,,
+BMGC_DS21667,BMG_DS080309,,,,,,,DOID:0081446,dimethylglycine dehydrogenase deficiency,,,605850,,,
+BMGC_DS21668,BMG_DS080310,,,,,,,DOID:0070616,glycine encephalopathy 1,,,605899,,,
+BMGC_DS21669,BMG_DS080311,,,,,,,DOID:0060369,Parkinson's disease 6,,,605909,,,
+BMGC_DS21670,BMG_DS080312,,,,,,,DOID:0081168,HMG-CoA synthase 2 deficiency,,,605911,,,
+BMGC_DS21671,BMG_DS080313,,,,,,,DOID:0050755,spinocerebellar ataxia with axonal neuropathy 2,,,606002,,,
+BMGC_DS21672,BMG_DS080314,,,,,,,DOID:0080354,Phelan-McDermid syndrome,,,606232,,,
+BMGC_DS21673,BMG_DS080315,,,,,,,DOID:0111104,maturity-onset diabetes of the young type 6,,,606394,,,
+BMGC_DS21674,BMG_DS080316,,,,,,,DOID:0080731,Ehlers-Danlos syndrome classic-like 1,,,606408,,,
+BMGC_DS21675,BMG_DS080317,,,,,,,DOID:0050991,episodic ataxia type 3,,,606554,,,
+BMGC_DS21676,BMG_DS080318,,,,,,,DOID:0070098,oculocutaneous albinism type IV,,,606574,,,
+BMGC_DS21677,BMG_DS080319,,,,,,,DOID:0060021,DNA ligase IV deficiency,,,606593,,,
+BMGC_DS21678,BMG_DS080320,,,,,,,DOID:0060195,amyotrophic lateral sclerosis type 3,,,606640,,,
+BMGC_DS21679,BMG_DS080321,,,,,,,DOID:0110951,Waardenburg syndrome type 2C,,,606662,,,
+BMGC_DS21680,BMG_DS080322,,,,,,,DOID:0060244,specific language impairment,,,606711;606712;607134;612514;615432,,,
+BMGC_DS21681,BMG_DS080323,,,,,,,DOID:0070217,familial hyperinsulinemic hypoglycemia 6,,,606762,,,
+BMGC_DS21682,BMG_DS080325,,,,,,,DOID:0110974,brachydactyly type A1B,,,607004,,,
+BMGC_DS21683,BMG_DS080326,,,,,,,DOID:0080559,congenital disorder of glycosylation Ig,,,607143,,,
+BMGC_DS21684,BMG_DS080327,,,,,,,DOID:0080422,Dravet syndrome,,,607208,,,
+BMGC_DS21685,BMG_DS080328,,,,,,,DOID:0050970,spinocerebellar ataxia type 19/22,,,607346,,,
+BMGC_DS21686,BMG_DS080329,,,,,,,DOID:0081178,autosomal recessive intellectual developmental disorder 2,,,607417,,,
+BMGC_DS21687,BMG_DS080330,,,,,,,DOID:0112237,lissencephaly 1,,,607432,,,
+BMGC_DS21688,BMG_DS080331,,,,,,,DOID:0111015,Newfoundland cone-rod dystrophy,,,607476,,,
+BMGC_DS21689,BMG_DS080332,,,,,,,DOID:0050650,familial atrial fibrillation,,,607554;608583;608988;611493;611494;612201;612240;613055;613980;614022;614049;614050;615377;615378;615770;PS608583,,,
+BMGC_DS21690,BMG_DS080333,,,,,,,DOID:0060265,pontocerebellar hypoplasia type 1A,,,607596,,,
+BMGC_DS21691,BMG_DS080334,,,,,,,DOID:0111312,idiopathic generalized epilepsy 11,,,607628,,,
+BMGC_DS21692,BMG_DS080335,,,,,,,DOID:0111324,juvenile absence epilepsy 1,,,607631,,,
+BMGC_DS21693,BMG_DS080336,,,,,,,DOID:0111202,autosomal dominant distal hereditary motor neuronopathy 14,,,607641,,,
+BMGC_DS21694,BMG_DS080337,,,,,,,DOID:0111323,idiopathic generalized epilepsy 9,,,607682,,,
+BMGC_DS21695,BMG_DS080338,,,,,,,DOID:0110042,Alzheimer's disease 3,,,607822,,,
+BMGC_DS21696,BMG_DS080339,,,,,,,DOID:0112245,focal segmental glomerulosclerosis 3,,,607832,,,
+BMGC_DS21697,BMG_DS080340,,,,,,,DOID:0111284,psoriasis 9,,,607857,,,
+BMGC_DS21698,BMG_DS080341,,,,,,,DOID:0111692,familial adult myoclonic epilepsy 2,,,607876,,,
+BMGC_DS21699,BMG_DS080342,,,,,,,DOID:0060198,amyotrophic lateral sclerosis type 6,,,608030,,,
+BMGC_DS21700,BMG_DS080343,,,,,,,DOID:0060199,amyotrophic lateral sclerosis type 7,,,608031,,,
+BMGC_DS21701,BMG_DS080344,,,,,,,DOID:0080562,congenital disorder of glycosylation Ij,,,608093,,,
+BMGC_DS21702,BMG_DS080345,,,,,,,DOID:0080560,congenital disorder of glycosylation Ih,,,608104,,,
+BMGC_DS21703,BMG_DS080346,,,,,,,DOID:0111645,Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome,,,608105,,,
+BMGC_DS21704,BMG_DS080347,,,,,,,DOID:0111712,Kagami-Ogata syndrome,,,608149,,,
+BMGC_DS21705,BMG_DS080348,,,,,,,DOID:0111793,congenital nystagmus 3,,,608345,,,
+BMGC_DS21706,BMG_DS080349,,,,,,,DOID:0111269,autosomal dominant hyaline body myopathy,,,608358,,,
+BMGC_DS21707,BMG_DS080350,,,,,,,DOID:0070290,primary autosomal recessive microcephaly 6,,,608393,,,
+BMGC_DS21708,BMG_DS080351,,,,,,,DOID:0111046,platelet-type bleeding disorder 10,,,608404,,,
+BMGC_DS21709,BMG_DS080352,,,,,,,DOID:0070363,bradyopsia 1,,,608415,,,
+BMGC_DS21710,BMG_DS080353,,,,,,,DOID:0081179,autosomal recessive intellectual developmental disorder 3,,,608443,,,
+BMGC_DS21711,BMG_DS080354,,,,,,,DOID:0080563,congenital disorder of glycosylation Ik,,,608540,,,
+BMGC_DS21712,BMG_DS080355,,,,,,,DOID:0080965,intracranial berry aneurysm 2,,,608542,,,
+BMGC_DS21713,BMG_DS080356,,,,,,,DOID:0050752,amyotrophic lateral sclerosis type 8,,,608627,,,
+BMGC_DS21714,BMG_DS080357,,,,,,,DOID:0111207,autosomal dominant distal hereditary motor neuronopathy 3,,,608634,,,
+BMGC_DS21715,BMG_DS080358,,,,,,,DOID:0112362,spondylocostal dysostosis 2,,,608681,,,
+BMGC_DS21716,BMG_DS080359,,,,,,,DOID:0070280,primary autosomal recessive microcephaly 5,,,608716,,,
+BMGC_DS21717,BMG_DS080360,,,,,,,DOID:0111318,idiopathic generalized epilepsy 3,,,608762,,,
+BMGC_DS21718,BMG_DS080361,,,,,,,DOID:0080564,congenital disorder of glycosylation Il,,,608776,,,
+BMGC_DS21719,BMG_DS080362,,,,,,,DOID:0080093,myofibrillar myopathy 2,,,608810,,,
+BMGC_DS21720,BMG_DS080363,,,,,,,DOID:0080593,orofacial cleft 6,,,608864,,,
+BMGC_DS21721,BMG_DS080364,,,,,,,DOID:0111364,Alzheimer's disease 9,,,608907,,,
+BMGC_DS21722,BMG_DS080365,,,,,,,DOID:0110679,congenital myasthenic syndrome 4C,,,608931,,,
+BMGC_DS21723,BMG_DS080366,,,,,,,DOID:0060864,patterned macular dystrophy 2,,,608970,,,
+BMGC_DS21724,BMG_DS080367,,,,,,,DOID:0111170,autosomal dominant sensory ataxia 1,,,608984,,,
+BMGC_DS21725,BMG_DS080368,,,,,,,DOID:0080860,primary ovarian insufficiency 3,,,608996,,,
+BMGC_DS21726,BMG_DS080369,,,,,,,DOID:0110244,cataract 28,,,609026,,,
+BMGC_DS21727,BMG_DS080370,,,,,,,DOID:0060470,salt and pepper syndrome,,,609056,,,
+BMGC_DS21728,BMG_DS080371,,,,,,,DOID:0081101,nonautoimmune hyperthyroidism,,,609152,,,
+BMGC_DS21729,BMG_DS080372,,,,,,,DOID:0070235,Loeys-Dietz syndrome 1,,,609192,,,
+BMGC_DS21730,BMG_DS080373,,,,,,,DOID:0112291,autosomal recessive spondyloepiphyseal dysplasia tarda Leroy-Spranger type,,,609223,,,
+BMGC_DS21731,BMG_DS080374,,,,,,,DOID:0112318,Schindler disease type 1,,,609241,,,
+BMGC_DS21732,BMG_DS080375,,,,,,,DOID:0112319,Kanzaki disease,,,609242,,,
+BMGC_DS21733,BMG_DS080376,,,,,,,DOID:0111309,familial febrile seizures 6,,,609253,,,
+BMGC_DS21734,BMG_DS080377,,,,,,,DOID:0111306,familial febrile seizures 5,,,609255,,,
+BMGC_DS21735,BMG_DS080378,,,,,,,DOID:0111517,autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2,,,609283,,,
+BMGC_DS21736,BMG_DS080379,,,,,,,DOID:0111520,autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3,,,609286,,,
+BMGC_DS21737,BMG_DS080380,,,,,,,DOID:0080440,developmental and epileptic encephalopathy 3,,,609304,,,
+BMGC_DS21738,BMG_DS080381,,,,,,,DOID:0070274,hereditary nonpolyposis colorectal cancer type 2,,,609310,,,
+BMGC_DS21739,BMG_DS080382,,,,,,,DOID:0060483,MEDNIK syndrome,,,609313,,,
+BMGC_DS21740,BMG_DS080383,,,,,,,DOID:0070618,rhabdoid tumor predisposition syndrome 1,,,609322,,,
+BMGC_DS21741,BMG_DS080384,,,,,,,DOID:0081019,congenital fibrosis of the extraocular muscles 3C,,,609384,,,
+BMGC_DS21742,BMG_DS080385,,,,,,,DOID:0080096,myofibrillar myopathy 5,,,609524,,,
+BMGC_DS21743,BMG_DS080386,,,,,,,DOID:0111426,restrictive cardiomyopathy 2,,,609578,,,
+BMGC_DS21744,BMG_DS080387,,,,,,,DOID:0050793,short QT syndrome,,,609620;609621;609622,,,
+BMGC_DS21745,BMG_DS080388,,,,,,,DOID:0080682,autosomal dominant familial visceral neuropathy,,,609629,,,
+BMGC_DS21746,BMG_DS080389,,,,,,,DOID:0111183,familial hemiplegic migraine 3,,,609634,,,
+BMGC_DS21747,BMG_DS080391,,,,,,,DOID:0111293,generalized epilepsy with febrile seizures plus 4,,,609800,,,
+BMGC_DS21748,BMG_DS080392,,,,,,,DOID:0112361,spondylocostal dysostosis 3,,,609813,,,
+BMGC_DS21749,BMG_DS080393,,,,,,,DOID:0080338,familial erythrocytosis 3,,,609820,,,
+BMGC_DS21750,BMG_DS080394,,,,,,,DOID:0070220,familial hyperinsulinemic hypoglycemia 5,,,609968,,,
+BMGC_DS21751,BMG_DS080395,,,,,,,DOID:0070215,familial hyperinsulinemic hypoglycemia 4,,,609975,,,
+BMGC_DS21752,BMG_DS080396,,,,,,,DOID:0070544,congenital glutamine deficiency,,,610015,,,
+BMGC_DS21753,BMG_DS080397,,,,,,,DOID:0111686,hereditary mixed polyposis syndrome 2,,,610069,,,
+BMGC_DS21754,BMG_DS080398,,,,,,,DOID:0111189,distal myopathy 3,,,610099,,,
+BMGC_DS21755,BMG_DS080399,,,,,,,DOID:0090069,giant axonal neuropathy 2,,,610100,,,
+BMGC_DS21756,BMG_DS080400,,,,,,,DOID:0111525,autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4,,,610131,,,
+BMGC_DS21757,BMG_DS080401,,,,,,,DOID:0110019,age related macular degeneration 7,,,610149,,,
+BMGC_DS21758,BMG_DS080402,,,,,,,DOID:0070234,Loeys-Dietz syndrome 2,,,610168,,,
+BMGC_DS21759,BMG_DS080403,,,,,,,DOID:0110000,3-methylglutaconic aciduria type 5,,,610198,,,
+BMGC_DS21760,BMG_DS080404,,,,,,,DOID:0060638,neonatal diabetes mellitus with congenital hypothyroidism,,,610199,,,
+BMGC_DS21761,BMG_DS080405,,,,,,,DOID:0080967,intracranial berry aneurysm 4,,,610213,,,
+BMGC_DS21762,BMG_DS080406,,,,,,,DOID:0110784,hereditary spastic paraplegia 33,,,610244,,,
+BMGC_DS21763,BMG_DS080407,,,,,,,DOID:0080607,anterior segment dysgenesis 2,,,610256,,,
+BMGC_DS21764,BMG_DS080408,,,,,,,DOID:0080330,cold-induced sweating syndrome 2,,,610313,,,
+BMGC_DS21765,BMG_DS080409,,,,,,,DOID:0050880,Koolen de Vries syndrome,,,610443,,,
+BMGC_DS21766,BMG_DS080410,,,,,,,DOID:0110715,congenital stationary night blindness autosomal dominant 3,,,610444,,,
+BMGC_DS21767,BMG_DS080411,,,,,,,DOID:0110862,congenital stationary night blindness autosomal dominant 1,,,610445,,,
+BMGC_DS21768,BMG_DS080412,,,,,,,DOID:0080170,normophosphatemic familial tumoral calcinosis,,,610455,,,
+BMGC_DS21769,BMG_DS080413,,,,,,,DOID:0061004,poor metabolism of thiopurines 1,,,610460,,,
+BMGC_DS21770,BMG_DS080414,,,,,,,DOID:0111106,maturity-onset diabetes of the young type 7,,,610508,,,
+BMGC_DS21771,BMG_DS080415,,,,,,,DOID:0080196,"mandibulofacial dysostosis, Guion-Almeida type",,,610536,,,
+BMGC_DS21772,BMG_DS080416,,,,,,,DOID:0110017,age related macular degeneration 4,,,610698,,,
+BMGC_DS21773,BMG_DS080417,,,,,,,DOID:0111288,psoriasis 8,,,610707,,,
+BMGC_DS21774,BMG_DS080418,,,,,,,DOID:0112133,severe congenital neutropenia 3,,,610738,,,
+BMGC_DS21775,BMG_DS080419,,,,,,,DOID:0080507,Cornelia de Lange syndrome 3,,,610759,,,
+BMGC_DS21776,BMG_DS080420,,,,,,,DOID:0080565,congenital disorder of glycosylation Im,,,610768,,,
+BMGC_DS21777,BMG_DS080421,,,,,,,DOID:0080206,CAKUT1,,,610805,,,
+BMGC_DS21778,BMG_DS080422,,,,,,,DOID:0111424,branchiootorenal syndrome 2,,,610896,,,
+BMGC_DS21779,BMG_DS080423,,,,,,,DOID:0050723,PSAT deficiency,,,610992,,,
+BMGC_DS21780,BMG_DS080424,,,,,,,DOID:0081180,autosomal recessive intellectual developmental disorder 12,,,611090,,,
+BMGC_DS21781,BMG_DS080425,,,,,,,DOID:0081181,autosomal recessive intellectual developmental disorder 5,,,611091,,,
+BMGC_DS21782,BMG_DS080426,,,,,,,DOID:0081182,autosomal recessive intellectual developmental disorder 6,,,611092,,,
+BMGC_DS21783,BMG_DS080427,,,,,,,DOID:0081183,autosomal recessive intellectual developmental disorder 7,,,611093,,,
+BMGC_DS21784,BMG_DS080428,,,,,,,DOID:0081184,autosomal recessive intellectual developmental disorder 9/26,,,611095,,,
+BMGC_DS21785,BMG_DS080429,,,,,,,DOID:0081185,autosomal recessive intellectual developmental disorder 10/20,,,611096,,,
+BMGC_DS21786,BMG_DS080430,,,,,,,DOID:0081186,autosomal recessive intellectual developmental disorder 11,,,611097,,,
+BMGC_DS21787,BMG_DS080431,,,,,,,DOID:0081187,autosomal recessive intellectual developmental disorder 4,,,611107,,,
+BMGC_DS21788,BMG_DS080432,,,,,,,DOID:0111314,idiopathic generalized epilepsy 13,,,611136,,,
+BMGC_DS21789,BMG_DS080433,,,,,,,DOID:0111812,syndromic microphthalmia 10,,,611222,,,
+BMGC_DS21790,BMG_DS080434,,,,,,,DOID:0050941,spastic ataxia 2,,,611302,,,
+BMGC_DS21791,BMG_DS080435,,,,,,,DOID:0060653,lethal congenital contracture syndrome 3,,,611369,,,
+BMGC_DS21792,BMG_DS080436,,,,,,,DOID:0110021,age related macular degeneration 9,,,611378,,,
+BMGC_DS21793,BMG_DS080437,,,,,,,DOID:0050942,spastic ataxia 3,,,611390,,,
+BMGC_DS21794,BMG_DS080438,,,,,,,DOID:0111430,essential tremor 3,,,611456,,,
+BMGC_DS21795,BMG_DS080439,,,,,,,DOID:0110022,age related macular degeneration 10,,,611488,,,
+BMGC_DS21796,BMG_DS080440,,,,,,,DOID:0110944,autosomal recessive osteopetrosis 4,,,611490,,,
+BMGC_DS21797,BMG_DS080441,,,,,,,DOID:0110945,autosomal recessive osteopetrosis 6,,,611497,,,
+BMGC_DS21798,BMG_DS080442,,,,,,,DOID:0111311,familial febrile seizures 7,,,611515,,,
+BMGC_DS21799,BMG_DS080443,,,,,,,DOID:0080862,primary ovarian insufficiency 5,,,611548,,,
+BMGC_DS21800,BMG_DS080444,,,,,,,DOID:0060750,familial temporal lobe epilepsy 3,,,611630,,,
+BMGC_DS21801,BMG_DS080445,,,,,,,DOID:0060753,familial temporal lobe epilepsy 4,,,611631,,,
+BMGC_DS21802,BMG_DS080446,,,,,,,DOID:0111303,familial febrile seizures 9,,,611634,,,
+BMGC_DS21803,BMG_DS080448,,,,,,,DOID:0081341,congenital myopathy 5,,,611705,,,
+BMGC_DS21804,BMG_DS080449,,,,,,,DOID:0080339,familial erythrocytosis 4,,,611783,,,
+BMGC_DS21805,BMG_DS080450,,,,,,,DOID:0080969,intracranial berry aneurysm 6,,,611892,,,
+BMGC_DS21806,BMG_DS080451,,,,,,,DOID:0060200,amyotrophic lateral sclerosis type 9,,,611895,,,
+BMGC_DS21807,BMG_DS080452,,,,,,,DOID:0050995,episodic ataxia type 7,,,611907,,,
+BMGC_DS21808,BMG_DS080454,,,,,,,DOID:0110023,age related macular degeneration 11,,,611953,,,
+BMGC_DS21809,BMG_DS080455,,,,,,,DOID:0080566,congenital disorder of glycosylation In,,,612015,,,
+BMGC_DS21810,BMG_DS080456,,,,,,,DOID:0060926,otosclerosis 8,,,612096,,,
+BMGC_DS21811,BMG_DS080457,,,,,,,DOID:0110317,hypertrophic cardiomyopathy 11,,,612098,,,
+BMGC_DS21812,BMG_DS080458,,,,,,,DOID:0081079,ectodermal dysplasia and immunodeficiency 2,,,612132,,,
+BMGC_DS21813,BMG_DS080459,,,,,,,DOID:0080970,intracranial berry aneurysm 7,,,612161,,,
+BMGC_DS21814,BMG_DS080460,,,,,,,DOID:0080971,intracranial berry aneurysm 8,,,612162,,,
+BMGC_DS21815,BMG_DS080461,,,,,,,DOID:0080436,developmental and epileptic encephalopathy 4,,,612164,,,
+BMGC_DS21816,BMG_DS080462,,,,,,,DOID:0111107,maturity-onset diabetes of the young type 9,,,612225,,,
+BMGC_DS21817,BMG_DS080463,,,,,,,DOID:0111161,Crouzon syndrome-acanthosis nigricans syndrome,,,612247,,,
+BMGC_DS21818,BMG_DS080464,,,,,,,DOID:0111300,generalized epilepsy with febrile seizures plus 6,,,612279,,,
+BMGC_DS21819,BMG_DS080465,,,,,,,DOID:0080863,primary ovarian insufficiency 6,,,612310,,,
+BMGC_DS21820,BMG_DS080466,,,,,,,DOID:0070052,autosomal dominant intellectual developmental disorder 22,,,612337,,,
+BMGC_DS21821,BMG_DS080467,,,,,,,DOID:0080739,Ehlers-Danlos syndrome spondylodysplastic type 3,,,612350,,,
+BMGC_DS21822,BMG_DS080468,,,,,,,DOID:0080568,congenital disorder of glycosylation Iq,,,612379,,,
+BMGC_DS21823,BMG_DS080469,,,,,,,DOID:0111289,psoriasis 10,,,612410,,,
+BMGC_DS21824,BMG_DS080470,,,,,,,DOID:0111427,restrictive cardiomyopathy 3,,,612422,,,
+BMGC_DS21825,BMG_DS080471,,,,,,,DOID:0111448,progressive myoclonus epilepsy 1B,,,612437,,,
+BMGC_DS21826,BMG_DS080472,,,,,,,DOID:0051013,pseudohypoparathyroidism type 1C,,,612462,,,
+BMGC_DS21827,BMG_DS080473,,,,,,,DOID:0080101,Compton-North congenital myopathy,,,612540,,,
+BMGC_DS21828,BMG_DS080474,,,,,,,DOID:0112136,severe congenital neutropenia 4,,,612541,,,
+BMGC_DS21829,BMG_DS080475,,,,,,,DOID:0070033,autosomal dominant intellectual developmental disorder 3,,,612580,,,
+BMGC_DS21830,BMG_DS080476,,,,,,,DOID:0070034,autosomal dominant intellectual developmental disorder 4,,,612581,,,
+BMGC_DS21831,BMG_DS080477,,,,,,,DOID:0080972,intracranial berry aneurysm 9,,,612586,,,
+BMGC_DS21832,BMG_DS080478,,,,,,,DOID:0080973,intracranial berry aneurysm 10,,,612587,,,
+BMGC_DS21833,BMG_DS080479,,,,,,,DOID:0111285,psoriasis 11,,,612599,,,
+BMGC_DS21834,BMG_DS080480,,,,,,,DOID:0070035,autosomal dominant intellectual developmental disorder 5,,,612621,,,
+BMGC_DS21835,BMG_DS080481,,,,,,,DOID:0081117,benign familial infantile seizures 4,,,612627,,,
+BMGC_DS21836,BMG_DS080482,,,,,,,DOID:0051004,congenital nonspherocytic hemolytic anemia 3,,,612631,,,
+BMGC_DS21837,BMG_DS080483,,,,,,,DOID:0111304,familial febrile seizures 10,,,612637,,,
+BMGC_DS21838,BMG_DS080484,,,,,,,DOID:0110919,hereditary spherocytosis type 4,,,612653,,,
+BMGC_DS21839,BMG_DS080485,,,,,,,DOID:0050994,episodic ataxia type 6,,,612656,,,
+BMGC_DS21840,BMG_DS080486,,,,,,,DOID:0080181,PHARC syndrome,,,612674,,,
+BMGC_DS21841,BMG_DS080487,,,,,,,DOID:0110920,hereditary spherocytosis type 5,,,612690,,,
+BMGC_DS21842,BMG_DS080488,,,,,,,DOID:0070278,primary autosomal recessive microcephaly 7,,,612703,,,
+BMGC_DS21843,BMG_DS080489,,,,,,,DOID:0050712,AGAT deficiency,,,612718,,,
+BMGC_DS21844,BMG_DS080490,,,,,,,DOID:0110912,leukocyte adhesion deficiency 3,,,612840,,,
+BMGC_DS21845,BMG_DS080491,,,,,,,DOID:0080755,autosomal dominant keratosis follicularis spinulosa decalvans,,,612843,,,
+BMGC_DS21846,BMG_DS080492,,,,,,,DOID:0111322,idiopathic generalized epilepsy 8,,,612899,,,
+BMGC_DS21847,BMG_DS080493,,,,,,,DOID:0081360,spastic quadriplegic cerebral palsy 2,,,612900,,,
+BMGC_DS21848,BMG_DS080494,,,,,,,DOID:0110802,hereditary spastic paraplegia 50,,,612936,,,
+BMGC_DS21849,BMG_DS080495,,,,,,,DOID:0111291,psoriasis 12,,,612950,,,
+BMGC_DS21850,BMG_DS080496,,,,,,,DOID:0081007,RNASET2-deficient cystic leukoencephalopathy,,,612951,,,
+BMGC_DS21851,BMG_DS080497,,,,,,,DOID:0080097,myofibrillar myopathy 6,,,612954,,,
+BMGC_DS21852,BMG_DS080498,,,,,,,DOID:0081319,multiple synostoses syndrome 3,,,612961,,,
+BMGC_DS21853,BMG_DS080499,,,,,,,DOID:0111772,"46,XY sex reversal 3",,,612965,,,
+BMGC_DS21854,BMG_DS080500,,,,,,,DOID:0070249,autosomal dominant Emery-Dreifuss muscular dystrophy 4,,,612998,,,
+BMGC_DS21855,BMG_DS080501,,,,,,,DOID:0070359,primary biliary cholangitis 2,,,613007,,,
+BMGC_DS21856,BMG_DS080502,,,,,,,DOID:0070360,primary biliary cholangitis 3,,,613008,,,
+BMGC_DS21857,BMG_DS080503,,,,,,,DOID:0061019,combined or isolated pituitary hormone deficiency 1,,,613038,,,
+BMGC_DS21858,BMG_DS080504,,,,,,,DOID:0111292,idiopathic generalized epilepsy 10,,,613060,,,
+BMGC_DS21859,BMG_DS080505,,,,,,,DOID:0110103,atopic dermatitis 7,,,613064,,,
+BMGC_DS21860,BMG_DS080506,,,,,,,DOID:0050719,cerebral folate receptor alpha deficiency,,,613068,,,
+BMGC_DS21861,BMG_DS080507,,,,,,,DOID:0111518,autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5,,,613077,,,
+BMGC_DS21862,BMG_DS080508,,,,,,,DOID:0050593,primary congenital glaucoma,,,613085;613086,,,
+BMGC_DS21863,BMG_DS080509,,,,,,,DOID:0110859,polycystic kidney disease 2,,,613095,,,
+BMGC_DS21864,BMG_DS080510,,,,,,,DOID:0110925,familial hemophagocytic lymphohistiocytosis 5,,,613101,,,
+BMGC_DS21865,BMG_DS080511,,,,,,,DOID:0112131,severe congenital neutropenia 2,,,613107,,,
+BMGC_DS21866,BMG_DS080512,,,,,,,DOID:0070150,hereditary sensory and autonomic neuropathy type 2B,,,613115,,,
+BMGC_DS21867,BMG_DS080513,,,,,,,DOID:0111242,congenital muscular dystrophy-dystroglycanopathy type A6,,,613154,,,
+BMGC_DS21868,BMG_DS080514,,,,,,,DOID:0060174,GABA aminotransferase deficiency,,,613163,,,
+BMGC_DS21869,BMG_DS080515,,,,,,,DOID:0081098,autosomal recessive intellectual developmental disorder 13,,,613192,,,
+BMGC_DS21870,BMG_DS080516,,,,,,,DOID:0080605,ankylosing spondylitis 3,,,613238,,,
+BMGC_DS21871,BMG_DS080517,,,,,,,DOID:0110319,hypertrophic cardiomyopathy 13,,,613243,,,
+BMGC_DS21872,BMG_DS080518,,,,,,,DOID:0110320,hypertrophic cardiomyopathy 14,,,613251,,,
+BMGC_DS21873,BMG_DS080519,,,,,,,DOID:0110954,Waardenburg syndrome type 4B,,,613265,,,
+BMGC_DS21874,BMG_DS080520,,,,,,,DOID:0110955,Waardenburg syndrome type 4C,,,613266,,,
+BMGC_DS21875,BMG_DS080521,,,,,,,DOID:0080536,hypermanganesemia with dystonia 1,,,613280,,,
+BMGC_DS21876,BMG_DS080522,,,,,,,DOID:0112304,spondylometaphyseal dysplasia Megarbane-Dagher-Melike type,,,613320,,,
+BMGC_DS21877,BMG_DS080523,,,,,,,DOID:0060997,rhabdoid tumor predisposition syndrome 2,,,613325,,,
+BMGC_DS21878,BMG_DS080524,,,,,,,DOID:0111108,maturity-onset diabetes of the young type 10,,,613370,,,
+BMGC_DS21879,BMG_DS080525,,,,,,,DOID:0050979,spinocerebellar ataxia type 30,,,613371,,,
+BMGC_DS21880,BMG_DS080526,,,,,,,DOID:0111109,maturity-onset diabetes of the young type 11,,,613375,,,
+BMGC_DS21881,BMG_DS080527,,,,,,,DOID:0060203,amyotrophic lateral sclerosis type 12,,,613435,,,
+BMGC_DS21882,BMG_DS080528,,,,,,,DOID:0070262,congenital disorder of glycosylation type IIj,,,613489,,,
+BMGC_DS21883,BMG_DS080529,,,,,,,DOID:0081146,common variable immunodeficiency 3,,,613493,,,
+BMGC_DS21884,BMG_DS080530,,,,,,,DOID:0080925,cytochrome P450 oxidoreductase deficiency,,,613571,,,
+BMGC_DS21885,BMG_DS080531,,,,,,,DOID:0070261,congenital disorder of glycosylation type IIi,,,613612,,,
+BMGC_DS21886,BMG_DS080532,,,,,,,DOID:0060647,fetal encasement syndrome,,,613630,,,
+BMGC_DS21887,BMG_DS080533,,,,,,,DOID:0070157,hereditary sensory and autonomic neuropathy type 1C,,,613640,,,
+BMGC_DS21888,BMG_DS080534,,,,,,,DOID:0111331,intellectual disability-severe speech delay-mild dysmorphism syndrome,,,613670,,,
+BMGC_DS21889,BMG_DS080535,,,,,,,DOID:0110018,age related macular degeneration 6,,,613757,,,
+BMGC_DS21890,BMG_DS080536,,,,,,,DOID:0080309,fatal infantile hypertonic myofibrillar myopathy,,,613869,,,
+BMGC_DS21891,BMG_DS080537,,,,,,,DOID:0070205,familial partial lipodystrophy type 4,,,613877,,,
+BMGC_DS21892,BMG_DS080538,,,,,,,DOID:0070091,schizophrenia 15,,,613950,,,
+BMGC_DS21893,BMG_DS080539,,,,,,,DOID:0070036,autosomal dominant intellectual developmental disorder 6,,,613970,,,
+BMGC_DS21894,BMG_DS080540,,,,,,,DOID:0070019,autosomal recessive dyskeratosis congenita 3,,,613988,,,
+BMGC_DS21895,BMG_DS080541,,,,,,,DOID:0070018,autosomal dominant dyskeratosis congenita 3,,,613990,,,
+BMGC_DS21896,BMG_DS080542,,,,,,,DOID:0081334,Nestor-Guillermo progeria syndrome,,,614008,,,
+BMGC_DS21897,BMG_DS080543,,,,,,,DOID:0111449,progressive myoclonus epilepsy 6,,,614018,,,
+BMGC_DS21898,BMG_DS080544,,,,,,,DOID:0081188,autosomal recessive intellectual developmental disorder 14,,,614020,,,
+BMGC_DS21899,BMG_DS080545,,,,,,,DOID:0050724,PSPH deficiency,,,614023,,,
+BMGC_DS21900,BMG_DS080546,,,,,,,DOID:0111287,psoriasis 13,,,614070,,,
+BMGC_DS21901,BMG_DS080547,,,,,,,DOID:0112224,chondrodysplasia with joint dislocations gPAPP type,,,614078,,,
+BMGC_DS21902,BMG_DS080548,,,,,,,DOID:0080138,multiple congenital anomalies-hypotonia-seizures syndrome 1,,,614080,,,
+BMGC_DS21903,BMG_DS080549,,,,,,,DOID:0111086,Fanconi anemia complementation group G,,,614082,,,
+BMGC_DS21904,BMG_DS080550,,,,,,,DOID:0111479,combined oxidative phosphorylation deficiency 8,,,614096,,,
+BMGC_DS21905,BMG_DS080551,,,,,,,DOID:0070037,autosomal dominant intellectual developmental disorder 7,,,614104,,,
+BMGC_DS21906,BMG_DS080552,,,,,,,DOID:0070032,autosomal dominant intellectual developmental disorder 2,,,614113,,,
+BMGC_DS21907,BMG_DS080553,,,,,,,DOID:0080142,mosaic variegated aneuploidy syndrome 2,,,614114,,,
+BMGC_DS21908,BMG_DS080554,,,,,,,DOID:0111356,hydrolethalus syndrome 2,,,614120,,,
+BMGC_DS21909,BMG_DS080555,,,,,,,DOID:0050983,spinocerebellar ataxia type 36,,,614153,,,
+BMGC_DS21910,BMG_DS080556,,,,,,,DOID:0111047,platelet-type bleeding disorder 14,,,614158,,,
+BMGC_DS21911,BMG_DS080557,,,,,,,DOID:0081189,autosomal recessive intellectual developmental disorder 16,,,614208,,,
+BMGC_DS21912,BMG_DS080558,,,,,,,DOID:0080063,autosomal recessive spinocerebellar ataxia 11,,,614229,,,
+BMGC_DS21913,BMG_DS080559,,,,,,,DOID:0081190,autosomal recessive intellectual developmental disorder 18,,,614249,,,
+BMGC_DS21914,BMG_DS080560,,,,,,,DOID:0070040,autosomal dominant intellectual developmental disorder 10,,,614256,,,
+BMGC_DS21915,BMG_DS080561,,,,,,,DOID:0111773,"46,XY sex reversal 8",,,614279,,,
+BMGC_DS21916,BMG_DS080562,,,,,,,DOID:0111328,juvenile myoclonic epilepsy 9,,,614280,,,
+BMGC_DS21917,BMG_DS080563,,,,,,,DOID:0080584,autosomal dominant Wolfram syndrome,,,614296,,,
+BMGC_DS21918,BMG_DS080564,,,,,,,DOID:0080134,multiple mitochondrial dysfunctions syndrome 2,,,614299,,,
+BMGC_DS21919,BMG_DS080565,,,,,,,DOID:0081191,autosomal recessive intellectual developmental disorder 31,,,614329,,,
+BMGC_DS21920,BMG_DS080566,,,,,,,DOID:0070273,hereditary nonpolyposis colorectal cancer type 6,,,614331,,,
+BMGC_DS21921,BMG_DS080567,,,,,,,DOID:0081192,autosomal recessive intellectual developmental disorder 29,,,614333,,,
+BMGC_DS21922,BMG_DS080568,,,,,,,DOID:0081194,autosomal recessive intellectual developmental disorder 33,,,614341,,,
+BMGC_DS21923,BMG_DS080569,,,,,,,DOID:0081195,autosomal recessive intellectual developmental disorder 30,,,614342,,,
+BMGC_DS21924,BMG_DS080570,,,,,,,DOID:0081196,autosomal recessive intellectual developmental disorder 23,,,614344,,,
+BMGC_DS21925,BMG_DS080571,,,,,,,DOID:0081197,autosomal recessive intellectual developmental disorder 24,,,614345,,,
+BMGC_DS21926,BMG_DS080572,,,,,,,DOID:0081198,autosomal recessive intellectual developmental disorder 25,,,614346,,,
+BMGC_DS21927,BMG_DS080573,,,,,,,DOID:0081199,autosomal recessive intellectual developmental disorder 28,,,614347,,,
+BMGC_DS21928,BMG_DS080574,,,,,,,DOID:0070276,hereditary nonpolyposis colorectal cancer type 7,,,614385,,,
+BMGC_DS21929,BMG_DS080575,,,,,,,DOID:0111333,early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome,,,614399,,,
+BMGC_DS21930,BMG_DS080576,,,,,,,DOID:0080569,congenital disorder of glycosylation Ir,,,614507,,,
+BMGC_DS21931,BMG_DS080577,,,,,,,DOID:0080445,developmental and epileptic encephalopathy 13,,,614558,,,
+BMGC_DS21932,BMG_DS080578,,,,,,,DOID:0050883,infantile cerebellar-retinal degeneration,,,614559,,,
+BMGC_DS21933,BMG_DS080579,,,,,,,DOID:0070264,congenital disorder of glycosylation type IIl,,,614576,,,
+BMGC_DS21934,BMG_DS080580,,,,,,,DOID:0111472,combined oxidative phosphorylation deficiency 9,,,614582,,,
+BMGC_DS21935,BMG_DS080581,,,,,,,DOID:0080508,Cornelia de Lange syndrome 4,,,614701,,,
+BMGC_DS21936,BMG_DS080582,,,,,,,DOID:0111480,combined oxidative phosphorylation deficiency 10,,,614702,,,
+BMGC_DS21937,BMG_DS080583,,,,,,,DOID:0080786,Brown-Vialetto-Van Laere syndrome 2,,,614707,,,
+BMGC_DS21938,BMG_DS080584,,,,,,,DOID:0070263,congenital disorder of glycosylation type IIk,,,614727,,,
+BMGC_DS21939,BMG_DS080585,,,,,,,DOID:0050885,IMAGe syndrome,,,614732,,,
+BMGC_DS21940,BMG_DS080586,,,,,,,DOID:0110001,"3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome",,,614739,,,
+BMGC_DS21941,BMG_DS080587,,,,,,,DOID:0080363,mitochondrial pyruvate carrier deficiency,,,614741,,,
+BMGC_DS21942,BMG_DS080588,,,,,,,DOID:0112102,Sotos syndrome 2,,,614753,,,
+BMGC_DS21943,BMG_DS080589,,,,,,,DOID:0111224,centronuclear myopathy 4,,,614807,,,
+BMGC_DS21944,BMG_DS080590,,,,,,,DOID:0111313,idiopathic generalized epilepsy 12,,,614847,,,
+BMGC_DS21945,BMG_DS080591,,,,,,,DOID:0080478,peroxisome biogenesis disorder 3A,,,614859,,,
+BMGC_DS21946,BMG_DS080592,,,,,,,DOID:0080479,peroxisome biogenesis disorder 4A,,,614862,,,
+BMGC_DS21947,BMG_DS080593,,,,,,,DOID:0080481,peroxisome biogenesis disorder 6A,,,614870,,,
+BMGC_DS21948,BMG_DS080594,,,,,,,DOID:0081435,Peroxisome biogenesis disorder 6B,,,614871,,,
+BMGC_DS21949,BMG_DS080595,,,,,,,DOID:0081436,Peroxisome biogenesis disorder 7B,,,614873,,,
+BMGC_DS21950,BMG_DS080596,,,,,,,DOID:0080483,peroxisome biogenesis disorder 8A,,,614876,,,
+BMGC_DS21951,BMG_DS080597,,,,,,,DOID:0081437,Peroxisome biogenesis disorder 8B,,,614877,,,
+BMGC_DS21952,BMG_DS080598,,,,,,,DOID:0081438,Peroxisome biogenesis disorder 9B,,,614879,,,
+BMGC_DS21953,BMG_DS080599,,,,,,,DOID:0111214,autosomal recessive distal hereditary motor neuronopathy 5,,,614881,,,
+BMGC_DS21954,BMG_DS080600,,,,,,,DOID:0080570,congenital disorder of glycosylation It,,,614921,,,
+BMGC_DS21955,BMG_DS080601,,,,,,,DOID:0111481,combined oxidative phosphorylation deficiency 11,,,614922,,,
+BMGC_DS21956,BMG_DS080602,,,,,,,DOID:0111493,combined oxidative phosphorylation deficiency 12,,,614924,,,
+BMGC_DS21957,BMG_DS080603,,,,,,,DOID:0111467,combined oxidative phosphorylation deficiency 13,,,614932,,,
+BMGC_DS21958,BMG_DS080604,,,,,,,DOID:0111477,combined oxidative phosphorylation deficiency 14,,,614946,,,
+BMGC_DS21959,BMG_DS080605,,,,,,,DOID:0111491,combined oxidative phosphorylation deficiency 15,,,614947,,,
+BMGC_DS21960,BMG_DS080606,,,,,,,DOID:0080439,developmental and epileptic encephalopathy 14,,,614959,,,
+BMGC_DS21961,BMG_DS080607,,,,,,,DOID:0070047,Schuurs-Hoeijmakers Syndrome,,,615009,,,
+BMGC_DS21962,BMG_DS080608,,,,,,,DOID:0080571,congenital disorder of glycosylation Iu,,,615042,,,
+BMGC_DS21963,BMG_DS080609,,,,,,,DOID:0111594,distal arthrogryposis type 5D,,,615065,,,
+BMGC_DS21964,BMG_DS080610,,,,,,,DOID:0081201,autosomal recessive intellectual developmental disorder 35,,,615162,,,
+BMGC_DS21965,BMG_DS080611,,,,,,,DOID:0081111,osteosclerotic metaphyseal dysplasia,,,615198,,,
+BMGC_DS21966,BMG_DS080612,,,,,,,DOID:0070093,schizophrenia 18,,,615232,,,
+BMGC_DS21967,BMG_DS080613,,,,,,,DOID:0070203,familial partial lipodystrophy type 5,,,615238,,,
+BMGC_DS21968,BMG_DS080614,,,,,,,DOID:0081099,"neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies",,,615286,,,
+BMGC_DS21969,BMG_DS080615,,,,,,,DOID:0070349,spinal muscular atrophy with lower extremity predominant 2A,,,615290,,,
+BMGC_DS21970,BMG_DS080616,,,,,,,DOID:0070099,oculocutaneous albinism type V,,,615312,,,
+BMGC_DS21971,BMG_DS080617,,,,,,,DOID:0080135,multiple mitochondrial dysfunctions syndrome 3,,,615330,,,
+BMGC_DS21972,BMG_DS080618,,,,,,,DOID:0112309,central precocious puberty 2,,,615346,,,
+BMGC_DS21973,BMG_DS080619,,,,,,,DOID:0080058,autosomal recessive spinocerebellar ataxia 14,,,615386,,,
+BMGC_DS21974,BMG_DS080620,,,,,,,DOID:0060019,coronin-1A deficiency,,,615401,,,
+BMGC_DS21975,BMG_DS080621,,,,,,,DOID:0080131,mitochondrial DNA depletion syndrome 13,,,615471,,,
+BMGC_DS21976,BMG_DS080622,,,,,,,DOID:0080893,Bainbridge-Ropers syndrome,,,615485,,,
+BMGC_DS21977,BMG_DS080623,,,,,,,DOID:0081202,autosomal recessive intellectual developmental disorder 37,,,615493,,,
+BMGC_DS21978,BMG_DS080624,,,,,,,DOID:0070051,autosomal dominant intellectual developmental disorder 21,,,615502,,,
+BMGC_DS21979,BMG_DS080625,,,,,,,DOID:0112321,"alacrima, achalasia, and impaired intellectual development syndrome",,,615510,,,
+BMGC_DS21980,BMG_DS080626,,,,,,,DOID:0111062,familial hypobetalipoproteinemia 1,,,615558,,,
+BMGC_DS21981,BMG_DS080627,,,,,,,DOID:0111210,autosomal dominant distal hereditary motor neuronopathy 6,,,615575,,,
+BMGC_DS21982,BMG_DS080628,,,,,,,DOID:0080573,congenital disorder of glycosylation Ix,,,615597,,,
+BMGC_DS21983,BMG_DS080629,,,,,,,DOID:0081206,autosomal recessive intellectual developmental disorder 41,,,615637,,,
+BMGC_DS21984,BMG_DS080630,,,,,,,DOID:0080057,autosomal recessive spinocerebellar ataxia 15,,,615705,,,
+BMGC_DS21985,BMG_DS080631,,,,,,,DOID:0112226,Bosch-Boonstra-Schaaf optic atrophy syndrome,,,615722,,,
+BMGC_DS21986,BMG_DS080632,,,,,,,DOID:0080431,developmental and epileptic encephalopathy 19,,,615744,,,
+BMGC_DS21987,BMG_DS080633,,,,,,,DOID:0070053,autosomal dominant intellectual developmental disorder 23,,,615761,,,
+BMGC_DS21988,BMG_DS080634,,,,,,,DOID:0081153,common variable immunodeficiency 11,,,615767,,,
+BMGC_DS21989,BMG_DS080635,,,,,,,DOID:0080029,autosomal recessive spinocerebellar ataxia 16,,,615768,,,
+BMGC_DS21990,BMG_DS080636,,,,,,,DOID:0060279,pontocerebellar hypoplasia type 10,,,615803,,,
+BMGC_DS21991,BMG_DS080637,,,,,,,DOID:0081207,autosomal recessive intellectual developmental disorder 43,,,615817,,,
+BMGC_DS21992,BMG_DS080638,,,,,,,DOID:0070056,autosomal dominant intellectual developmental disorder 26,,,615834,,,
+BMGC_DS21993,BMG_DS080639,,,,,,,DOID:0080328,Culler-Jones syndrome,,,615849,,,
+BMGC_DS21994,BMG_DS080640,,,,,,,DOID:0070058,Helsmoortel-Van Der Aa Syndrome,,,615873,,,
+BMGC_DS21995,BMG_DS080641,,,,,,,DOID:0070224,progressive familial intrahepatic cholestasis 4,,,615878,,,
+BMGC_DS21996,BMG_DS080642,,,,,,,DOID:0112339,Tatton-Brown-Rahman syndrome,,,615879,,,
+BMGC_DS21997,BMG_DS080643,,,,,,,DOID:0080407,orofacial cleft 14,,,615892,,,
+BMGC_DS21998,BMG_DS080644,,,,,,,DOID:0080453,developmental and epileptic encephalopathy 25,,,615905,,,
+BMGC_DS21999,BMG_DS080645,,,,,,,DOID:0111465,combined oxidative phosphorylation deficiency 21,,,615918,,,
+BMGC_DS22000,BMG_DS080646,,,,,,,DOID:0081208,autosomal recessive intellectual developmental disorder 44,,,615942,,,
+BMGC_DS22001,BMG_DS080647,,,,,,,DOID:0060958,orofaciodigital syndrome XIV,,,615948,,,
+BMGC_DS22002,BMG_DS080648,,,,,,,DOID:0050985,spinocerebellar ataxia type 38,,,615957,,,
+BMGC_DS22003,BMG_DS080649,,,,,,,DOID:0081209,autosomal recessive intellectual developmental disorder 45,,,615979,,,
+BMGC_DS22004,BMG_DS080650,,,,,,,DOID:0070206,familial partial lipodystrophy type 6,,,615980,,,
+BMGC_DS22005,BMG_DS080651,,,,,,,DOID:0112134,severe congenital neutropenia 6,,,616022,,,
+BMGC_DS22006,BMG_DS080652,,,,,,,DOID:0050986,spinocerebellar ataxia type 40,,,616053,,,
+BMGC_DS22007,BMG_DS080653,,,,,,,DOID:0050996,episodic ataxia type 8,,,616055,,,
+BMGC_DS22008,BMG_DS080654,,,,,,,DOID:0080461,developmental and epileptic encephalopathy 26,,,616056,,,
+BMGC_DS22009,BMG_DS080655,,,,,,,DOID:0070059,autosomal dominant intellectual developmental disorder 29,,,616078,,,
+BMGC_DS22010,BMG_DS080656,,,,,,,DOID:0112381,muscular dystrophy-dystroglycanopathy type C12,,,616094,,,
+BMGC_DS22011,BMG_DS080657,,,,,,,DOID:0111281,psoriasis 15,,,616106,,,
+BMGC_DS22012,BMG_DS080658,,,,,,,DOID:0081210,autosomal recessive intellectual developmental disorder 46,,,616116,,,
+BMGC_DS22013,BMG_DS080659,,,,,,,DOID:0080064,autosomal recessive spinocerebellar ataxia 17,,,616127,,,
+BMGC_DS22014,BMG_DS080660,,,,,,,DOID:0081243,rhizomelic chondrodysplasia punctate type 4,,,616154,,,
+BMGC_DS22015,BMG_DS080661,,,,,,,DOID:0111500,combined oxidative phosphorylation deficiency 23,,,616198,,,
+BMGC_DS22016,BMG_DS080662,,,,,,,DOID:0111264,Ruijs-Aalfs syndrome,,,616200,,,
+BMGC_DS22017,BMG_DS080663,,,,,,,DOID:0060339,chronic atrial and intestinal dysrhythmia,,,616201,,,
+BMGC_DS22018,BMG_DS080664,,,,,,,DOID:0081357,isolated mitochondrial myopathy,,,616209,,,
+BMGC_DS22019,BMG_DS080665,,,,,,,DOID:0112236,lissencephaly 6,,,616212,,,
+BMGC_DS22020,BMG_DS080666,,,,,,,DOID:0111451,progressive myoclonus epilepsy 8,,,616230,,,
+BMGC_DS22021,BMG_DS080667,,,,,,,DOID:0111485,combined oxidative phosphorylation deficiency 24,,,616239,,,
+BMGC_DS22022,BMG_DS080668,,,,,,,DOID:0081048,congenital limbs-face contractures-hypotonia-developmental delay syndrome,,,616266,,,
+BMGC_DS22023,BMG_DS080669,,,,,,,DOID:0070062,Arboleda-Tham syndrome,,,616268,,,
+BMGC_DS22024,BMG_DS080670,,,,,,,DOID:0081212,autosomal recessive intellectual developmental disorder 48,,,616269,,,
+BMGC_DS22025,BMG_DS080671,,,,,,,DOID:0070244,primary coenzyme Q10 deficiency 7,,,616276,,,
+BMGC_DS22026,BMG_DS080672,,,,,,,DOID:0111066,congenital bile acid synthesis defect 5,,,616278,,,
+BMGC_DS22027,BMG_DS080673,,,,,,,DOID:0080065,autosomal recessive spinocerebellar ataxia 19,,,616291,,,
+BMGC_DS22028,BMG_DS080674,,,,,,,DOID:0070063,autosomal dominant intellectual developmental disorder 33,,,616311,,,
+BMGC_DS22029,BMG_DS080675,,,,,,,DOID:0080437,developmental and epileptic encephalopathy 31A,,,616346,,,
+BMGC_DS22030,BMG_DS080676,,,,,,,DOID:0070064,autosomal dominant intellectual developmental disorder 34,,,616351,,,
+BMGC_DS22031,BMG_DS080677,,,,,,,DOID:0080066,autosomal recessive spinocerebellar ataxia 20,,,616354,,,
+BMGC_DS22032,BMG_DS080678,,,,,,,DOID:0070066,autosomal dominant intellectual developmental disorder 36,,,616362,,,
+BMGC_DS22033,BMG_DS080679,,,,,,,DOID:0070067,White-Sutton syndrome,,,616364,,,
+BMGC_DS22034,BMG_DS080680,,,,,,,DOID:0080416,developmental and epileptic encephalopathy 32,,,616366,,,
+BMGC_DS22035,BMG_DS080681,,,,,,,DOID:0060365,mandibulofacial dysostosis with alopecia,,,616367,,,
+BMGC_DS22036,BMG_DS080682,,,,,,,DOID:0080136,multiple mitochondrial dysfunctions syndrome 4,,,616370,,,
+BMGC_DS22037,BMG_DS080683,,,,,,,DOID:0070068,autosomal dominant intellectual developmental disorder 38,,,616393,,,
+BMGC_DS22038,BMG_DS080684,,,,,,,DOID:0111744,cerebellar ataxia type 41,,,616410,,,
+BMGC_DS22039,BMG_DS080685,,,,,,,DOID:0081242,"autoimmune interstitial lung, joint, and kidney disease",,,616414,,,
+BMGC_DS22040,BMG_DS080686,,,,,,,DOID:0060788,hypomyelinating leukodystrophy 10,,,616420,,,
+BMGC_DS22041,BMG_DS080687,,,,,,,DOID:0060475,myoclonic-atonic epilepsy,,,616421,,,
+BMGC_DS22042,BMG_DS080688,,,,,,,DOID:0111468,combined oxidative phosphorylation deficiency 25,,,616430,,,
+BMGC_DS22043,BMG_DS080689,,,,,,,DOID:0110819,hereditary spastic paraplegia 74,,,616451,,,
+BMGC_DS22044,BMG_DS080690,,,,,,,DOID:0080419,developmental and epileptic encephalopathy 50,,,616457,,,
+BMGC_DS22045,BMG_DS080691,,,,,,,DOID:0081213,autosomal recessive intellectual developmental disorder 50,,,616460,,,
+BMGC_DS22046,BMG_DS080692,,,,,,,DOID:0070153,hereditary sensory and autonomic neuropathy type 8,,,616488,,,
+BMGC_DS22047,BMG_DS080693,,,,,,,DOID:0110178,Charcot-Marie-Tooth disease axonal type 2V,,,616491,,,
+BMGC_DS22048,BMG_DS080694,,,,,,,DOID:0081447,cone-rod dystrophy 21,,,616502,,,
+BMGC_DS22049,BMG_DS080695,,,,,,,DOID:0070248,autosomal recessive Emery-Dreifuss muscular dystrophy 3,,,616516,,,
+BMGC_DS22050,BMG_DS080696,,,,,,,DOID:0111490,combined oxidative phosphorylation deficiency 26,,,616539,,,
+BMGC_DS22051,BMG_DS080697,,,,,,,DOID:0111450,progressive myoclonus epilepsy 9,,,616540,,,
+BMGC_DS22052,BMG_DS080698,,,,,,,DOID:0080592,Klippel-Feil syndrome 4,,,616549,,,
+BMGC_DS22053,BMG_DS080699,,,,,,,DOID:0112281,spondyloepiphyseal dysplasia Stanescu type,,,616583,,,
+BMGC_DS22054,BMG_DS080700,,,,,,,DOID:0111940,immunodeficiency 42,,,616622,,,
+BMGC_DS22055,BMG_DS080701,,,,,,,DOID:0110162,"Charcot-Marie-Tooth disease, axonal type 2W",,,616625,,,
+BMGC_DS22056,BMG_DS080702,,,,,,,DOID:0080458,developmental and epileptic encephalopathy 35,,,616647,,,
+BMGC_DS22057,BMG_DS080703,,,,,,,DOID:0110176,Charcot-Marie-Tooth disease axonal type 2X,,,616668,,,
+BMGC_DS22058,BMG_DS080704,,,,,,,DOID:0111489,combined oxidative phosphorylation deficiency 27,,,616672,,,
+BMGC_DS22059,BMG_DS080705,,,,,,,DOID:0111315,idiopathic generalized epilepsy 14,,,616685,,,
+BMGC_DS22060,BMG_DS080706,,,,,,,DOID:0110181,Charcot-Marie-Tooth disease axonal type 2Z,,,616688,,,
+BMGC_DS22061,BMG_DS080707,,,,,,,DOID:0110854,rhizomelic chondrodysplasia punctata type 5,,,616716,,,
+BMGC_DS22062,BMG_DS080708,,,,,,,DOID:0070266,congenital disorder of glycosylation type IIn,,,616721,,,
+BMGC_DS22063,BMG_DS080709,,,,,,,DOID:0112243,congenital symmetric circumferential skin creases 2,,,616734,,,
+BMGC_DS22064,BMG_DS080710,,,,,,,DOID:0080408,orofacial cleft 15,,,616788,,,
+BMGC_DS22065,BMG_DS080711,,,,,,,DOID:0111470,combined oxidative phosphorylation deficiency 28,,,616794,,,
+BMGC_DS22066,BMG_DS080712,,,,,,,DOID:0111742,cerebellar ataxia type 42,,,616795,,,
+BMGC_DS22067,BMG_DS080713,,,,,,,DOID:0111501,combined oxidative phosphorylation deficiency 29,,,616811,,,
+BMGC_DS22068,BMG_DS080714,,,,,,,DOID:0110290,autosomal recessive limb-girdle muscular dystrophy type 2X,,,616812,,,
+BMGC_DS22069,BMG_DS080715,,,,,,,DOID:0110288,autosomal recessive limb-girdle muscular dystrophy type 2W,,,616827,,,
+BMGC_DS22070,BMG_DS080716,,,,,,,DOID:0070267,congenital disorder of glycosylation type IIo,,,616828,,,
+BMGC_DS22071,BMG_DS080717,,,,,,,DOID:0070268,congenital disorder of glycosylation type IIp,,,616829,,,
+BMGC_DS22072,BMG_DS080718,,,,,,,DOID:0081386,TANGO2-related metabolic encephalopathy and arrythmias,,,616878,,,
+BMGC_DS22073,BMG_DS080719,,,,,,,DOID:0070477,diphthamide deficiency syndrome 1,,,616901,,,
+BMGC_DS22074,BMG_DS080720,,,,,,,DOID:0060996,poor metabolism of thiopurines 2,,,616903,,,
+BMGC_DS22075,BMG_DS080721,,,,,,,DOID:0110821,hereditary spastic paraplegia 76,,,616907,,,
+BMGC_DS22076,BMG_DS080722,,,,,,,DOID:0111613,autosomal recessive spinocerebellar ataxia 23,,,616949,,,
+BMGC_DS22077,BMG_DS080723,,,,,,,DOID:0070072,autosomal dominant intellectual developmental disorder 42,,,616973,,,
+BMGC_DS22078,BMG_DS080724,,,,,,,DOID:0111471,combined oxidative phosphorylation deficiency 30,,,616974,,,
+BMGC_DS22079,BMG_DS080725,,,,,,,DOID:0070073,autosomal dominant intellectual developmental disorder 43,,,616977,,,
+BMGC_DS22080,BMG_DS080726,,,,,,,DOID:0080537,hypermanganesemia with dystonia 2,,,617013,,,
+BMGC_DS22081,BMG_DS080727,,,,,,,DOID:0080163,otulipenia,,,617099,,,
+BMGC_DS22082,BMG_DS080728,,,,,,,DOID:0080454,developmental and epileptic encephalopathy 42,,,617106,,,
+BMGC_DS22083,BMG_DS080729,,,,,,,DOID:0060865,patterned macular dystrophy 3,,,617111,,,
+BMGC_DS22084,BMG_DS080730,,,,,,,DOID:0080456,developmental and epileptic encephalopathy 46,,,617162,,,
+BMGC_DS22085,BMG_DS080731,,,,,,,DOID:0081008,intellectual developmental disorder with cardiac arrhythmia,,,617173,,,
+BMGC_DS22086,BMG_DS080732,,,,,,,DOID:0081395,Harel-Yoon syndrome,,,617183,,,
+BMGC_DS22087,BMG_DS080733,,,,,,,DOID:0081219,autosomal recessive intellectual developmental disorder 57,,,617188,,,
+BMGC_DS22088,BMG_DS080734,,,,,,,DOID:0070423,early onset progressive encephalopathy with brain atrophy and thin corpus callosum,,,617193,,,
+BMGC_DS22089,BMG_DS080735,,,,,,,DOID:0112348,hereditary spastic paraplegia 78,,,617225,,,
+BMGC_DS22090,BMG_DS080736,,,,,,,DOID:0080762,autosomal recessive limb-girdle muscular dystrophy type 2Z,,,617232,,,
+BMGC_DS22091,BMG_DS080737,,,,,,,DOID:0081220,autosomal recessive intellectual developmental disorder 58,,,617270,,,
+BMGC_DS22092,BMG_DS080738,,,,,,,DOID:0081419,childhood-onset dystonia with optic atrophy and basal ganglia abnormalities,,,617282,,,
+BMGC_DS22093,BMG_DS080739,,,,,,,DOID:0080953,amelogenesis imperfecta type 1J,,,617297,,,
+BMGC_DS22094,BMG_DS080740,,,,,,,DOID:0080613,anterior segment dysgenesis 8,,,617319,,,
+BMGC_DS22095,BMG_DS080741,,,,,,,DOID:0081221,autosomal recessive intellectual developmental disorder 59,,,617323,,,
+BMGC_DS22096,BMG_DS080742,,,,,,,DOID:0070269,congenital disorder of glycosylation type IIq,,,617395,,,
+BMGC_DS22097,BMG_DS080743,,,,,,,DOID:0081222,autosomal recessive intellectual developmental disorder 60,,,617432,,,
+BMGC_DS22098,BMG_DS080744,,,,,,,DOID:0111764,"46,XX sex reversal 4",,,617480,,,
+BMGC_DS22099,BMG_DS080745,,,,,,,DOID:0112008,pituitary adenoma 5,,,617540,,,
+BMGC_DS22100,BMG_DS080746,,,,,,,DOID:0080252,spastic ataxia 8,,,617560,,,
+BMGC_DS22101,BMG_DS080747,,,,,,,DOID:0080258,autosomal recessive congenital ichthyosis 14,,,617571,,,
+BMGC_DS22102,BMG_DS080748,,,,,,,DOID:0080257,autosomal recessive congenital ichthyosis 13,,,617574,,,
+BMGC_DS22103,BMG_DS080749,,,,,,,DOID:0080236,autosomal dominant intellectual developmental disorder 45,,,617600,,,
+BMGC_DS22104,BMG_DS080750,,,,,,,DOID:0080237,autosomal dominant intellectual developmental disorder 46,,,617601,,,
+BMGC_DS22105,BMG_DS080751,,,,,,,DOID:0080274,multiple mitochondrial dysfunctions syndrome 5,,,617613,,,
+BMGC_DS22106,BMG_DS080752,,,,,,,DOID:0080281,schizophrenia 19,,,617629,,,
+BMGC_DS22107,BMG_DS080753,,,,,,,DOID:0080238,autosomal dominant intellectual developmental disorder 47,,,617635,,,
+BMGC_DS22108,BMG_DS080754,,,,,,,DOID:0112010,pituitary adenoma 3,,,617686,,,
+BMGC_DS22109,BMG_DS080755,,,,,,,DOID:0112324,pontocerebellar hypoplasia type 11,,,617695,,,
+BMGC_DS22110,BMG_DS080756,,,,,,,DOID:0070002,3-methylglutaconic aciduria type 9,,,617698,,,
+BMGC_DS22111,BMG_DS080757,,,,,,,DOID:0111495,combined oxidative phosphorylation deficiency 33,,,617713,,,
+BMGC_DS22112,BMG_DS080758,,,,,,,DOID:0070302,multiple epiphyseal dysplasia 7,,,617719,,,
+BMGC_DS22113,BMG_DS080759,,,,,,,DOID:0080235,autosomal dominant intellectual developmental disorder 48,,,617751,,,
+BMGC_DS22114,BMG_DS080760,,,,,,,DOID:0080287,spinocerebellar ataxia 45,,,617769,,,
+BMGC_DS22115,BMG_DS080761,,,,,,,DOID:0080288,spinocerebellar ataxia 46,,,617770,,,
+BMGC_DS22116,BMG_DS080762,,,,,,,DOID:0080239,autosomal recessive intellectual developmental disorder 61,,,617773,,,
+BMGC_DS22117,BMG_DS080763,,,,,,,DOID:0080233,autosomal dominant intellectual developmental disorder 50,,,617787,,,
+BMGC_DS22118,BMG_DS080764,,,,,,,DOID:0080232,autosomal dominant intellectual developmental disorder 51,,,617788,,,
+BMGC_DS22119,BMG_DS080765,,,,,,,DOID:0080231,autosomal dominant intellectual developmental disorder 52,,,617796,,,
+BMGC_DS22120,BMG_DS080766,,,,,,,DOID:0080228,autosomal dominant intellectual developmental disorder 53,,,617798,,,
+BMGC_DS22121,BMG_DS080767,,,,,,,DOID:0080230,autosomal dominant intellectual developmental disorder 54,,,617799,,,
+BMGC_DS22122,BMG_DS080768,,,,,,,DOID:0111727,geleophysic dysplasia 3,,,617809,,,
+BMGC_DS22123,BMG_DS080769,,,,,,,DOID:0111993,immunodeficiency 55,,,617827,,,
+BMGC_DS22124,BMG_DS080770,,,,,,,DOID:0080225,amyotrophic lateral sclerosis type 23,,,617839,,,
+BMGC_DS22125,BMG_DS080771,,,,,,,DOID:0080226,autosomal dominant intellectual developmental disorder 56,,,617854,,,
+BMGC_DS22126,BMG_DS080772,,,,,,,DOID:0111497,combined oxidative phosphorylation deficiency 34,,,617872,,,
+BMGC_DS22127,BMG_DS080773,,,,,,,DOID:0081378,amyotrophic lateral sclerosis type 24,,,617892,,,
+BMGC_DS22128,BMG_DS080774,,,,,,,DOID:0081379,amyotrophic lateral sclerosis type 25,,,617921,,,
+BMGC_DS22129,BMG_DS080775,,,,,,,DOID:0111325,juvenile myoclonic epilepsy 10,,,617924,,,
+BMGC_DS22130,BMG_DS080776,,,,,,,DOID:0060961,orofaciodigital syndrome XVIII,,,617927,,,
+BMGC_DS22131,BMG_DS080777,,,,,,,DOID:0070332,multiple mitochondrial dysfunctions syndrome 6,,,617954,,,
+BMGC_DS22132,BMG_DS080778,,,,,,,DOID:0080732,Ehlers-Danlos syndrome classic-like 2,,,618000,,,
+BMGC_DS22133,BMG_DS080779,,,,,,,DOID:0081224,autosomal recessive intellectual developmental disorder 63,,,618095,,,
+BMGC_DS22134,BMG_DS080780,,,,,,,DOID:0081225,autosomal recessive intellectual developmental disorder 64,,,618103,,,
+BMGC_DS22135,BMG_DS080781,,,,,,,DOID:0081226,autosomal recessive intellectual developmental disorder 65,,,618109,,,
+BMGC_DS22136,BMG_DS080782,,,,,,,DOID:0112207,developmental and epileptic encephalopathy 71,,,618328,,,
+BMGC_DS22137,BMG_DS080783,,,,,,,DOID:0111316,idiopathic generalized epilepsy 15,,,618357,,,
+BMGC_DS22138,BMG_DS080784,,,,,,,DOID:0112209,developmental and epileptic encephalopathy 73,,,618379,,,
+BMGC_DS22139,BMG_DS080785,,,,,,,DOID:0112200,spondyloepimetaphyseal dysplasia with joint laxity type 3,,,618395,,,
+BMGC_DS22140,BMG_DS080786,,,,,,,DOID:0111475,combined oxidative phosphorylation deficiency 39,,,618397,,,
+BMGC_DS22141,BMG_DS080787,,,,,,,DOID:0081346,congenital myopathy 14,,,618414,,,
+BMGC_DS22142,BMG_DS080788,,,,,,,DOID:0110649,long QT syndrome 8,,,618447,,,
+BMGC_DS22143,BMG_DS080789,,,,,,,DOID:0111836,congenital nongoitrous hypothyroidism 7,,,618573,,,
+BMGC_DS22144,BMG_DS080790,,,,,,,DOID:0112288,spondyloepiphyseal dysplasia Nishimura type,,,618618,,,
+BMGC_DS22145,BMG_DS080791,,,,,,,DOID:0111855,primary ciliary dyskinesia 42,,,618695,,,
+BMGC_DS22146,BMG_DS080792,,,,,,,DOID:0112014,congenital megabladder,,,618719,,,
+BMGC_DS22147,BMG_DS080793,,,,,,,DOID:0112117,combined oxidative phosphorylation deficiency 40,,,618835,,,
+BMGC_DS22148,BMG_DS080794,,,,,,,DOID:0060969,galactosemia 4,,,618881,,,
+BMGC_DS22149,BMG_DS080795,,,,,,,DOID:0081298,oculopharyngodistal myopathy 2,,,618940,,,
+BMGC_DS22150,BMG_DS080796,,,,,,,DOID:0112303,spondylometaphyseal dysplasia with corneal dystrophy,,,618961,,,
+BMGC_DS22151,BMG_DS080797,,,,,,,DOID:0080952,AMED syndrome,,,619151,,,
+BMGC_DS22152,BMG_DS080798,,,,,,,DOID:0112306,Mahvash Disease,,,619290,,,
+BMGC_DS22153,BMG_DS080799,,,,,,,DOID:0081233,autosomal recessive intellectual developmental disorder 73,,,619717,,,
+BMGC_DS22154,BMG_DS080800,,,,,,,DOID:0081235,autosomal recessive intellectual developmental disorder 76,,,619931,,,
+BMGC_DS22155,BMG_DS080801,,,,,,,DOID:0081236,autosomal recessive intellectual developmental disorder 77,,,619988,,,
+BMGC_DS22156,BMG_DS080802,,,,,,,DOID:0070393,developmental and epileptic encephalopathy 107,,,620033,,,
+BMGC_DS22157,BMG_DS080803,,,,,,,DOID:0070454,hereditary spastic paraplegia 70,,,620323,,,
+BMGC_DS22158,BMG_DS080804,,,,,,,DOID:0070366,nevoid basal cell carcinoma syndrome 2,,,620343,,,
+BMGC_DS22159,BMG_DS080805,,,,,,,DOID:0070364,bradyopsia 2,,,620344,,,
+BMGC_DS22160,BMG_DS080806,,,,,,,DOID:0070551,epidermolytic palmoplantar keratoderma 2,,,620411,,,
+BMGC_DS22161,BMG_DS080807,,,,,,,DOID:0070594,spermatogenic failure 95,,,620917,,,
+BMGC_DS22162,BMG_DS080808,,,,,,,DOID:0051002,congenital dyserythropoietic anemia type IVb,,,620969,,,
+BMGC_DS22163,BMG_DS080809,,,,,,,DOID:0050639,primary cutaneous amyloidosis,,,PS105250,,,
+BMGC_DS22164,BMG_DS080810,,,,,,,DOID:0060228,intracranial berry aneurysm,,,PS105800,,,
+BMGC_DS22165,BMG_DS080811,,,,,,,DOID:0050646,distal arthrogryposis,,,PS108120,,,
+BMGC_DS22166,BMG_DS080812,,,,,,,DOID:0080046,Stickler syndrome,,,PS108300,,,
+BMGC_DS22167,BMG_DS080813,,,,,,,DOID:0060669,cerebral cavernous malformation,,,PS116860,,,
+BMGC_DS22168,BMG_DS080814,,,,,,,DOID:0050567,orofacial cleft,,,PS119530,,,
+BMGC_DS22169,BMG_DS080815,,,,,,,DOID:0111297,familial febrile seizures,,,PS121210,,,
+BMGC_DS22170,BMG_DS080816,,,,,,,DOID:0080033,craniometaphyseal dysplasia,,,PS123000,,,
+BMGC_DS22171,BMG_DS080817,,,,,,,DOID:0080724,Kenny-Caffey syndrome,,,PS127000,,,
+BMGC_DS22172,BMG_DS080818,,,,,,,DOID:0070438,retinal macular dystrophy,,,PS136550,,,
+BMGC_DS22173,BMG_DS080819,,,,,,,DOID:0081073,Teebi hypertelorism syndrome,,,PS145420,,,
+BMGC_DS22174,BMG_DS080820,,,,,,,DOID:0080545,hyper IgE syndrome,,,PS147060,,,
+BMGC_DS22175,BMG_DS080821,,,,,,,DOID:0081370,LADD syndrome,,,PS149730,,,
+BMGC_DS22176,BMG_DS080822,,,,,,,DOID:0060307,autosomal dominant intellectual developmental disorder,,,PS156200,,,
+BMGC_DS22177,BMG_DS080823,,,,,,,DOID:0112241,multiple benign circumferential skin creases on limbs,,,PS156610,,,
+BMGC_DS22178,BMG_DS080824,,,,,,,DOID:0070348,spinal muscular atrophy with lower extremity predominant,,,PS158600,,,
+BMGC_DS22179,BMG_DS080825,,,,,,,DOID:0080683,nonsyndromic congenital nail disorder,,,PS161050,,,
+BMGC_DS22180,BMG_DS080826,,,,,,,DOID:0081296,oculopharyngodistal myopathy,,,PS164310,,,
+BMGC_DS22181,BMG_DS080827,,,,,,,DOID:0080322,polycystic kidney disease,,,PS173900,,,
+BMGC_DS22182,BMG_DS080828,,,,,,,DOID:0112313,brain small vessel disease,,,PS175780,,,
+BMGC_DS22183,BMG_DS080829,,,,,,,DOID:0081332,progeroid syndrome,,,PS176670,,,
+BMGC_DS22184,BMG_DS080830,,,,,,,DOID:0111198,autosomal dominant distal hereditary motor neuronopathy,,,PS182960,,,
+BMGC_DS22185,BMG_DS080831,,,,,,,DOID:0050788,proximal symphalangism,,,PS185800,,,
+BMGC_DS22186,BMG_DS080832,,,,,,,DOID:0050794,multiple synostoses syndrome,,,PS186500,,,
+BMGC_DS22187,BMG_DS080833,,,,,,,DOID:0080620,familial glucocorticoid deficiency,,,PS202200,,,
+BMGC_DS22188,BMG_DS080834,,,,,,,DOID:0080627,alopecia-mental retardation syndrome,,,PS203650,,,
+BMGC_DS22189,BMG_DS080835,,,,,,,DOID:0050763,ARC syndrome,,,PS208085,,,
+BMGC_DS22190,BMG_DS080836,,,,,,,DOID:0050710,3-methylcrotonyl-CoA carboxylase deficiency,,,PS210200,,,
+BMGC_DS22191,BMG_DS080837,,,,,,,DOID:0050570,congenital disorder of glycosylation type I,,,PS212065,,,
+BMGC_DS22192,BMG_DS080838,,,,,,,DOID:0050950,autosomal recessive cerebellar ataxia,,,PS213200,,,
+BMGC_DS22193,BMG_DS080839,,,,,,,DOID:0081072,"craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome",,,PS213980,,,
+BMGC_DS22194,BMG_DS080840,,,,,,,DOID:0080377,peroxisomal biogenesis disorder,,,PS214100,,,
+BMGC_DS22195,BMG_DS080841,,,,,,,DOID:0080910,cerebrooculofacioskeletal syndrome,,,PS214150,,,
+BMGC_DS22196,BMG_DS080842,,,,,,,DOID:0060774,congenital diarrhea,,,PS214700,,,
+BMGC_DS22197,BMG_DS080843,,,,,,,DOID:0111229,congenital muscular dystrophy-dystroglycanopathy type A,,,PS236670,,,
+BMGC_DS22198,BMG_DS080844,,,,,,,DOID:0070230,benign recurrent intrahepatic cholestasis,,,PS243300,,,
+BMGC_DS22199,BMG_DS080845,,,,,,,DOID:0060229,Baraitser-Winter syndrome,,,PS243310,,,
+BMGC_DS22200,BMG_DS080846,,,,,,,DOID:0081127,mandibuloacral dysplasia,,,PS248370,,,
+BMGC_DS22201,BMG_DS080847,,,,,,,DOID:0060308,autosomal recessive intellectual developmental disorder,,,PS249500,,,
+BMGC_DS22202,BMG_DS080848,,,,,,,DOID:0070296,primary autosomal recessive microcephaly,,,PS251200,,,
+BMGC_DS22203,BMG_DS080849,,,,,,,DOID:0112065,nuclear type mitochondrial complex I deficiency,,,PS252010,,,
+BMGC_DS22204,BMG_DS080850,,,,,,,DOID:0060913,proteosome-associated autoinflammatory syndrome,,,PS256040,,,
+BMGC_DS22205,BMG_DS080851,,,,,,,DOID:0111910,spermatogenic failure,,,PS258150,,,
+BMGC_DS22206,BMG_DS080852,,,,,,,DOID:0050877,pancreatic agenesis,,,PS260370,,,
+BMGC_DS22207,BMG_DS080853,,,,,,,DOID:0111862,congenital bilateral absence of vas deferens,,,PS277180,,,
+BMGC_DS22208,BMG_DS080854,,,,,,,DOID:0050568,spondylocostal dysostosis,,,PS277300,,,
+BMGC_DS22209,BMG_DS080855,,,,,,,DOID:0081077,ectodermal dysplasia and immune deficiency,,,PS300291,,,
+BMGC_DS22210,BMG_DS080856,,,,,,,DOID:0050798,cerebral creatine deficiency syndrome,,,PS300352,,,
+BMGC_DS22211,BMG_DS080857,,,,,,,DOID:0060704,lymphoproliferative syndrome,,,PS308240,,,
+BMGC_DS22212,BMG_DS080858,,,,,,,DOID:0112202,developmental and epileptic encephalopathy,,,PS308350,,,
+BMGC_DS22213,BMG_DS080859,,,,,,,DOID:0060309,syndromic X-linked intellectual disability,,,PS309510,,,
+BMGC_DS22214,BMG_DS080860,,,,,,,DOID:0080636,syndromic microphthalmia,,,PS309800,,,
+BMGC_DS22215,BMG_DS080861,,,,,,,DOID:0111875,MLS syndrome,,,PS309801,,,
+BMGC_DS22216,BMG_DS080862,,,,,,,DOID:0060786,hypomyelinating leukodystrophy,,,PS312080,,,
+BMGC_DS22217,BMG_DS080863,,,,,,,DOID:0111757,Y-linked deafness,,,PS400043,,,
+BMGC_DS22218,BMG_DS080864,,,,,,,DOID:0050575,D-2-hydroxyglutaric aciduria,,,PS600721,,,
+BMGC_DS22219,BMG_DS080865,,,,,,,DOID:0060169,benign familial infantile epilepsy,,,PS601764,,,
+BMGC_DS22220,BMG_DS080866,,,,,,,DOID:0070329,mitochondrial DNA depletion syndrome,,,PS603041,,,
+BMGC_DS22221,BMG_DS080867,,,,,,,DOID:0111197,autosomal recessive distal hereditary motor neuronopathy,,,PS604320,,,
+BMGC_DS22222,BMG_DS080868,,,,,,,DOID:0050628,advanced sleep phase syndrome,,,PS604348,,,
+BMGC_DS22223,BMG_DS080869,,,,,,,DOID:0081420,familial focal epilepsy with variable foci,,,PS604364,,,
+BMGC_DS22224,BMG_DS080870,,,,,,,DOID:0050730,coenzyme Q10 deficiency disease,,,PS607426,,,
+BMGC_DS22225,BMG_DS080871,,,,,,,DOID:0050585,congenital generalized lipodystrophy,,,PS608594,,,
+BMGC_DS22226,BMG_DS080872,,,,,,,DOID:0060286,combined oxidative phosphorylation deficiency,,,PS609060,,,
+BMGC_DS22227,BMG_DS080873,,,,,,,DOID:0080597,Kleefstra syndrome,,,PS610253,,,
+BMGC_DS22228,BMG_DS080874,,,,,,,DOID:0080655,hypophosphatemic nephrolithiasis/osteoporosis,,,PS612286,,,
+BMGC_DS22229,BMG_DS080875,,,,,,,DOID:0112375,muscular dystrophy-dystroglycanopathy type B,,,PS613155,,,
+BMGC_DS22230,BMG_DS080876,,,,,,,DOID:0080535,hypermanganesemia with dystonia,,,PS613280,,,
+BMGC_DS22231,BMG_DS080877,,,,,,,DOID:0081104,hot water epilepsy,,,PS613339,,,
+BMGC_DS22232,BMG_DS080878,,,,,,,DOID:0090131,complex cortical dysplasia with other brain malformations,,,PS614039,,,
+BMGC_DS22233,BMG_DS080879,,,,,,,DOID:0080503,multiple congenital anomalies-hypotonia-seizures syndrome,,,PS614080,,,
+BMGC_DS22234,BMG_DS080880,,,,,,,DOID:0111728,familial episodic pain syndrome,,,PS615040,,,
+BMGC_DS22235,BMG_DS080881,,,,,,,DOID:0080716,infantile liver failure syndrome,,,PS615438,,,
+BMGC_DS22236,BMG_DS080882,,,,,,,DOID:0070476,diphthamide deficiency syndrome,,,PS616901,,,
+BMGC_DS22237,BMG_DS080883,,,,,,,DOID:0080954,arthrogryposis multiplex congenita,,,PS617468,,,
+BMGC_DS22238,BMG_DS080884,,,,,,,DOID:0051010,Bryant-Li-Bhoj neurodevelopmental syndrome,,,PS619720,,,
+BMGC_DS22239,BMG_DS080904,,,,1A11.Z,"Botulism, unspecified",A05.1,,,,,,,,
+BMGC_DS22240,BMG_DS080952,,,,1B96/1G40,,A26.7,,,,,,,,
+BMGC_DS22241,BMG_DS080976,,,,XN6BM/1G40,,A41.0,,,,,,,,
+BMGC_DS22242,BMG_DS080978,,,,XN1P6/1G40,,A41.3,,,,,,,,
+BMGC_DS22243,BMG_DS081114,,,,1C62.0,HIV disease clinical stage 1 without mention of tuberculosis or malaria,B23.0,,,,,,,,
+BMGC_DS22244,BMG_DS081117,,,,1D82.Y/CA40.1Z,,B25.0,,,,,,,,
+BMGC_DS22245,BMG_DS081174,,,,1F51.Z/1D00.2,,B56.9,,,,,,,,
+BMGC_DS22246,BMG_DS081227,,,,XN3PW,Streptococcus pneumoniae,B95.3,,,,,,,,
+BMGC_DS22247,BMG_DS081342,,,,2C12.02,Hepatocellular carcinoma of liver,C22.0,,,,,,,,
+BMGC_DS22248,BMG_DS081907,,,,02,,D37.0,,,,,,,,
+BMGC_DS22249,BMG_DS081908,,,,02,,D37.1,,,,,,,,
+BMGC_DS22250,BMG_DS081909,,,,02,,D37.2,,,,,,,,
+BMGC_DS22251,BMG_DS081910,,,,02,,D37.3,,,,,,,,
+BMGC_DS22252,BMG_DS081911,,,,02,,D37.4,,,,,,,,
+BMGC_DS22253,BMG_DS081912,,,,02,,D37.5,,,,,,,,
+BMGC_DS22254,BMG_DS081913,,,,02,,D37.6,,,,,,,,
+BMGC_DS22255,BMG_DS081914,,,,02,,D37.7,,,,,,,,
+BMGC_DS22256,BMG_DS081916,,,,02,,D38.0,,,,,,,,
+BMGC_DS22257,BMG_DS081917,,,,02,,D38.1,,,,,,,,
+BMGC_DS22258,BMG_DS081918,,,,02,,D38.2,,,,,,,,
+BMGC_DS22259,BMG_DS081919,,,,02,,D38.3,,,,,,,,
+BMGC_DS22260,BMG_DS081920,,,,02,,D38.4,,,,,,,,
+BMGC_DS22261,BMG_DS081921,,,,02,,D38.5,,,,,,,,
+BMGC_DS22262,BMG_DS081922,,,,02,,D38.6,,,,,,,,
+BMGC_DS22263,BMG_DS081923,,,,02,,D39.0,,,,,,,,
+BMGC_DS22264,BMG_DS081924,,,,02,,D39.1,,,,,,,,
+BMGC_DS22265,BMG_DS081925,,,,02,,D39.2,,,,,,,,
+BMGC_DS22266,BMG_DS081926,,,,02,,D39.7,,,,,,,,
+BMGC_DS22267,BMG_DS081927,,,,02,,D39.9,,,,,,,,
+BMGC_DS22268,BMG_DS081928,,,,02,,D40.0,,,,,,,,
+BMGC_DS22269,BMG_DS081929,,,,02,,D40.1,,,,,,,,
+BMGC_DS22270,BMG_DS081930,,,,02,,D40.7,,,,,,,,
+BMGC_DS22271,BMG_DS081931,,,,02,,D40.9,,,,,,,,
+BMGC_DS22272,BMG_DS081932,,,,02,,D41.0,,,,,,,,
+BMGC_DS22273,BMG_DS081933,,,,02,,D41.1,,,,,,,,
+BMGC_DS22274,BMG_DS081934,,,,02,,D41.2,,,,,,,,
+BMGC_DS22275,BMG_DS081935,,,,02,,D41.3,,,,,,,,
+BMGC_DS22276,BMG_DS081936,,,,02,,D41.4,,,,,,,,
+BMGC_DS22277,BMG_DS081937,,,,02,,D41.7,,,,,,,,
+BMGC_DS22278,BMG_DS081938,,,,02,,D41.9,,,,,,,,
+BMGC_DS22279,BMG_DS081949,,,,02,,D44.0,,,,,,,,
+BMGC_DS22280,BMG_DS081950,,,,02,,D44.1,,,,,,,,
+BMGC_DS22281,BMG_DS081951,,,,02,,D44.2,,,,,,,,
+BMGC_DS22282,BMG_DS081952,,,,02,,D44.3,,,,,,,,
+BMGC_DS22283,BMG_DS081953,,,,02,,D44.4,,,,,,,,
+BMGC_DS22284,BMG_DS081954,,,,02,,D44.5,,,,,,,,
+BMGC_DS22285,BMG_DS081955,,,,02,,D44.6,,,,,,,,
+BMGC_DS22286,BMG_DS081956,,,,02,,D44.7,,,,,,,,
+BMGC_DS22287,BMG_DS081957,,,,02,,D44.8,,,,,,,,
+BMGC_DS22288,BMG_DS081958,,,,02,,D44.9,,,,,,,,
+BMGC_DS22289,BMG_DS081972,,,,2B3Z,"Neoplasms of haematopoietic or lymphoid tissues, unspecified",D47.7,DOID:0060888,transient myeloproliferative syndrome,,,,,,
+BMGC_DS22290,BMG_DS081973,,,,2B3Z,"Neoplasms of haematopoietic or lymphoid tissues, unspecified",D47.9,DOID:0060708;DOID:0110116;DOID:0060707,lymphoproliferative syndrome 2 | lymphoproliferative syndrome 1 | autoimmune lymphoproliferative syndrome type 2B,,,,,,
+BMGC_DS22291,BMG_DS081974,,,,02,,D48.0,,,,,,,,
+BMGC_DS22292,BMG_DS081975,,,,02,,D48.1,,,,,,,,
+BMGC_DS22293,BMG_DS081976,,,,02,,D48.2,,,,,,,,
+BMGC_DS22294,BMG_DS081977,,,,02,,D48.3,,,,,,,,
+BMGC_DS22295,BMG_DS081978,,,,02,,D48.4,,,,,,,,
+BMGC_DS22296,BMG_DS081979,,,,02,,D48.5,,,,,,,,
+BMGC_DS22297,BMG_DS081980,,,,02,,D48.6,,,,,,,,
+BMGC_DS22298,BMG_DS081981,,,,02,,D48.7,,,,,,,,
+BMGC_DS22299,BMG_DS081982,,,,02,,D48.9,,,,,,,,
+BMGC_DS22300,BMG_DS082038,,,,3B62.0Y,Other specified inherited qualitative platelet defects,D82.0,,,,,,,,
+BMGC_DS22301,BMG_DS082039,,,,4A01.34,Hyperimmunoglobulin E syndromes,D82.4,,,,,,,,
+BMGC_DS22302,BMG_DS082082,,,,5A11,Type 2 diabetes mellitus,E11.8,DOID:0050524,maturity-onset diabetes of the young,,,,,,
+BMGC_DS22303,BMG_DS082121,,,,5A70.1,Ectopic ACTH syndrome,E24.3,DOID:0060890,ectopic Cushing syndrome,,,,,,
+BMGC_DS22304,BMG_DS082136,,,,5A92,Peripheral precocious puberty,E30.1,DOID:0090122,aromatase excess syndrome,,,,,,
+BMGC_DS22305,BMG_DS082179,,,,5B81.Z,"Obesity, unspecified",E66.9,,,,,,,,
+BMGC_DS22306,BMG_DS082187,,,,5C52.0Z,"Inborn errors of fatty acid oxidation or ketone body metabolism, unspecified",E71.3,DOID:0090031;DOID:0090129,D-bifunctional protein deficiency | carnitine palmitoyltransferase I deficiency,,,,,,
+BMGC_DS22307,BMG_DS082189,,,,5C50.B,Disorders of methionine cycle or sulphur amino acid metabolism,E72.1,DOID:0111038;DOID:0111039;DOID:0111037,hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | glycine N-methyltransferase deficiency | hypermethioninemia due to adenosine kinase deficiency,,,,,,
+BMGC_DS22308,BMG_DS082197,,,,5C51.3,Glycogen storage disease,E74.0,DOID:0111040;DOID:0111042,glycogen storage disease IXd | glycogen storage disease IXa,,,,,,
+BMGC_DS22309,BMG_DS082198,,,,,,E74.0;G73.6,DOID:0090101,lethal congenital glycogen storage disease of heart,,,,,,
+BMGC_DS22310,BMG_DS082204,,,,5C56.1,Neuronal ceroid lipofuscinosis,E75.4,DOID:0110720;DOID:0110732;DOID:0110725;DOID:0110724;DOID:0110722;DOID:0110728;DOID:0110733;DOID:0110731;DOID:0110723;DOID:0110726;DOID:0110727;DOID:0110721;DOID:0110729;DOID:0110730,neuronal ceroid lipofuscinosis 13 | neuronal ceroid lipofuscinosis 8 | neuronal ceroid lipofuscinosis 9 | neuronal ceroid lipofuscinosis 5 | neuronal ceroid lipofuscinosis 10 | neuronal ceroid lipofuscinosis 6A | neuronal ceroid lipofuscinosis 6B | neuronal ceroid lipofuscinosis 11 | neuronal ceroid lipofuscinosis 8 northern epilepsy variant | neuronal ceroid lipofuscinosis 3 | neuronal ceroid lipofuscinosis 7 | neuronal ceroid lipofuscinosis 2 | neuronal ceroid lipofuscinosis 1 | neuronal ceroid lipofuscinosis 4,,,,,,
+BMGC_DS22311,BMG_DS082206,,,,5C56.30,Mucopolysaccharidosis type 1,E76.0,DOID:0060222,Scheie syndrome,,,,,,
+BMGC_DS22312,BMG_DS082211,,,,5C80.00,Primary hypercholesterolaemia,E78.0,DOID:0090105,autosomal recessive hypercholesterolemia,,,,,,
+BMGC_DS22313,BMG_DS082223,,,,5C64.1Z,"Disorders of iron metabolism, unspecified",E83.1,DOID:0111029;DOID:0111033;DOID:0111031,hemochromatosis type 1 | African iron overload | hemochromatosis type 5,,,,,,
+BMGC_DS22314,BMG_DS082225,,,,5C64.4Z,"Disorders of magnesium metabolism, unspecified",E83.4,DOID:0060885;DOID:0060879;DOID:0060884;DOID:0060883;DOID:0060880;DOID:0060882,renal hypomagnesemia 2 | renal hypomagnesemia 4 | intestinal hypomagnesemia 1 | primary hypomagnesemia | renal hypomagnesemia 3 | renal hypomagnesemia 6,,,,,,
+BMGC_DS22315,BMG_DS082226,,,,5C64.5,Disorders of calcium metabolism,E83.5,DOID:0060699;DOID:0060701;DOID:0060700;DOID:0060702,familial hypocalciuric hypercalcemia 3 | familial hypocalciuric hypercalcemia 2 | familial hypocalciuric hypercalcemia | familial hypocalciuric hypercalcemia 1,,,,,,
+BMGC_DS22316,BMG_DS082230,,,,5D00.21,Nonneuropathic heredofamilial amyloidosis,E85.0,DOID:0090029;DOID:0090018,TNF receptor–associated periodic syndrome | CINCA Syndrome,,,,,,
+BMGC_DS22317,BMG_DS082251,,,,6D81,Dementia due to cerebrovascular disease,F01.1,DOID:0111035;DOID:0111036,CADASIL 1 | CADASIL 2,,,,,,
+BMGC_DS22318,BMG_DS082273,,,,6D71,Mild neurocognitive disorder,F06.7,,,,,,,,
+BMGC_DS22319,BMG_DS082454,,,,6B40,Post traumatic stress disorder,F43.1,,,,,,,,
+BMGC_DS22320,BMG_DS082479,,,,6B80.Z,"Anorexia Nervosa, unspecified",F50.0,,,,,,,,
+BMGC_DS22321,BMG_DS082556,,,,6A00.1,"Disorder of intellectual development, moderate",F71.1,DOID:0060827,X-linked intellectual disability-psychosis-macroorchidism syndrome,,,,,,
+BMGC_DS22322,BMG_DS082559,,,,,,F72,DOID:0060823,syndromic X-linked intellectual disability 94,,,,,,
+BMGC_DS22323,BMG_DS082590,,,,LD90.4,Rett syndrome,F84.2,,,,,,,,
+BMGC_DS22324,BMG_DS082646,,,,,,G10,DOID:0090104;DOID:0090103,Huntington's disease-like 2 | Huntington's disease-like 1,,,,,,
+BMGC_DS22325,BMG_DS082648,,,,8A03.Z,"Ataxic disorders, unspecified",G11.1,DOID:0060792;DOID:0060797;DOID:0060794,hypomyelinating leukodystrophy 11 | hypomyelinating leukodystrophy 8 | hypomyelinating leukodystrophy 7,,,,,,
+BMGC_DS22326,BMG_DS082650,,,,8B44.0Z,"Hereditary spastic paraplegia, unspecified",G11.4,DOID:0110795;DOID:0110793;DOID:0110809;DOID:0110785;DOID:0110787;DOID:0110794;DOID:0110789;DOID:0110811;DOID:0110823;DOID:0110774;DOID:0110813;DOID:0110820;DOID:0110771;DOID:0110772;DOID:0110800;DOID:0110766;DOID:0110790;DOID:0110791;DOID:0110773;DOID:0110767;DOID:0110782;DOID:0110816;DOID:0110824;DOID:0110781;DOID:0110765;DOID:0110798;DOID:0110797;DOID:0110777;DOID:0110780;DOID:0050886;DOID:0110792;DOID:0110764;DOID:0110806;DOID:0110776;DOID:0110801;DOID:0110810;DOID:0110775;DOID:0110805;DOID:0110808;DOID:0110768;DOID:0110783;DOID:0110796;DOID:0110807;DOID:0110818;DOID:0110822;DOID:0110817;DOID:0110825;DOID:0110815;DOID:0110763;DOID:0110779;DOID:0110812;DOID:0110769;DOID:0110788;DOID:0110786;DOID:0110778;DOID:0110814;DOID:0110770,hereditary spastic paraplegia 32 | Troyer syndrome | hereditary spastic paraplegia 56 | hereditary spastic paraplegia 17 | hereditary spastic paraplegia 7 | hereditary spastic paraplegia 11 | hereditary spastic paraplegia 12 | hereditary spastic paraplegia 30 | hereditary spastic paraplegia 34 | hereditary spastic paraplegia 39 | hereditary spastic paraplegia 49 | hereditary spastic paraplegia 10 | hereditary spastic paraplegia 62 | hereditary spastic paraplegia 36 | hereditary spastic paraplegia 4 | hereditary spastic paraplegia 9B | hereditary spastic paraplegia 75 | hereditary spastic paraplegia 29 | hereditary spastic paraplegia 57 | hereditary spastic paraplegia 27 | hereditary spastic paraplegia 54 | hereditary spastic paraplegia 63 | hereditary spastic paraplegia 37 | hereditary spastic paraplegia 48 | hereditary spastic paraplegia 73 | hereditary spastic paraplegia 72A | hereditary spastic paraplegia 6 | hereditary spastic paraplegia 19 | hereditary spastic paraplegia 5A | hereditary spastic paraplegia 3A | hereditary spastic paraplegia 45 | hereditary spastic paraplegia 42 | hereditary spastic paraplegia 38 | hereditary spastic paraplegia 14 | hereditary spastic paraplegia 77 | hereditary spastic paraplegia 43 | hereditary spastic paraplegia 25 | hereditary spastic paraplegia 18 | hereditary spastic paraplegia 55 | hereditary spastic paraplegia 64 | hereditary spastic paraplegia 9A | hereditary spastic paraplegia 8 | hereditary spastic paraplegia 16 | hereditary spastic paraplegia 2 | hereditary spastic paraplegia 41 | hereditary spastic paraplegia 46 | hereditary spastic paraplegia 15 | hereditary spastic paraplegia 28 | hereditary spastic paraplegia 26 | hereditary spastic paraplegia 31 | hereditary spastic paraplegia 44 | hereditary spastic paraplegia 35 | hereditary spastic paraplegia 24 | hereditary spastic paraplegia 13 | hereditary spastic paraplegia 53 | hereditary spastic paraplegia 61 | hereditary spastic paraplegia 23,,,,,,
+BMGC_DS22327,BMG_DS082652,,,,8B60.Z,"Motor neuron disease, unspecified",G12.2,DOID:0060193;DOID:0060194;DOID:0111064;DOID:0060196,amyotrophic lateral sclerosis type 2 | amyotrophic lateral sclerosis type 1 | autosomal recessive distal hereditary motor neuronopathy 1 | amyotrophic lateral sclerosis type 4,,,,,,
+BMGC_DS22328,BMG_DS082658,,,,5C64.10,Iron overload diseases,G23.0,DOID:0110740;DOID:0110735;DOID:0110739;DOID:0110738;DOID:0110736,neurodegeneration with brain iron accumulation 6 | neurodegeneration with brain iron accumulation 2a | neurodegeneration with brain iron accumulation 2b | neurodegeneration with brain iron accumulation 4 | neurodegeneration with brain iron accumulation 5,,,,,,
+BMGC_DS22329,BMG_DS082683,,,,8A4Z,"Multiple sclerosis or other white matter disorders, unspecified",G37.8,DOID:0060793,hypomyelinating leukodystrophy 5,,,,,,
+BMGC_DS22330,BMG_DS082707,,,,8B10.Z,"Transient ischaemic attack, unspecified",G45.9,,,,,,,,
+BMGC_DS22331,BMG_DS082765,,,,8C03.Y/5D2Z,,G63.3,,,,,,,,
+BMGC_DS22332,BMG_DS082768,,,,8C03.Y/FC0Z,,G63.6,,,,,,,,
+BMGC_DS22333,BMG_DS082773,,,,8C70.Z,"Muscular dystrophy, unspecified",G71.0,DOID:0110297;DOID:0110279;DOID:0110285;DOID:0110282;DOID:0110275;DOID:0110284;DOID:0110283;DOID:0110287;DOID:0110277;DOID:0110304;DOID:0110292;DOID:0080092;DOID:0110289;DOID:0110299;DOID:0110274;DOID:0110294;DOID:0110280;DOID:0110278;DOID:0110295;DOID:0110303;DOID:0110293;DOID:0070247;DOID:0110281;DOID:0110276;DOID:0110306;DOID:0110296;DOID:0110298;DOID:0110305;DOID:0110273,autosomal recessive limb-girdle muscular dystrophy type 2P | autosomal recessive limb-girdle muscular dystrophy type 2K | autosomal recessive limb-girdle muscular dystrophy type 2Y | autosomal recessive limb-girdle muscular dystrophy type 2O | autosomal recessive limb-girdle muscular dystrophy type 2T | autosomal recessive limb-girdle muscular dystrophy type 2A | autosomal dominant limb-girdle muscular dystrophy type 3 | autosomal recessive limb-girdle muscular dystrophy type 2G | autosomal dominant limb-girdle muscular dystrophy type 2 | autosomal recessive limb-girdle muscular dystrophy type 2S | autosomal recessive limb-girdle muscular dystrophy type 2F | autosomal recessive limb-girdle muscular dystrophy type 2H | autosomal recessive limb-girdle muscular dystrophy type 2L | autosomal dominant limb-girdle muscular dystrophy type 1 | autosomal dominant limb-girdle muscular dystrophy type 1H | autosomal recessive limb-girdle muscular dystrophy type 2Q | autosomal recessive limb-girdle muscular dystrophy type 2U | autosomal recessive limb-girdle muscular dystrophy type 2E | autosomal recessive limb-girdle muscular dystrophy type 2J | autosomal recessive limb-girdle muscular dystrophy type 2C | myofibrillar myopathy 1 | autosomal recessive limb-girdle muscular dystrophy | autosomal recessive limb-girdle muscular dystrophy type 2B | autosomal recessive limb-girdle muscular dystrophy type 2M | autosomal dominant limb-girdle muscular dystrophy | autosomal dominant Emery-Dreifuss muscular dystrophy 2 | autosomal recessive limb-girdle muscular dystrophy type 2D | autosomal recessive limb-girdle muscular dystrophy type 2N | autosomal recessive limb-girdle muscular dystrophy type 2I,,,,,,
+BMGC_DS22334,BMG_DS082774,,,,8C71.Z,"Myotonic disorders, unspecified",G71.1,DOID:0090005,Schwartz-Jampel syndrome 1,,,,,,
+BMGC_DS22335,BMG_DS082775,,,,8C72.Z,"Congenital myopathies, unspecified",G71.2,DOID:0110635;DOID:0110640;DOID:0110639;DOID:0110637;DOID:0110634;DOID:0110632;DOID:0112374,congenital muscular dystrophy due to integrin alpha-7 deficiency | muscular dystrophy-dystroglycanopathy type B5 | congenital muscular dystrophy 1B | megaconial type congenital muscular dystrophy | muscular dystrophy-dystroglycanopathy | congenital muscular dystrophy due to LMNA mutation | muscular dystrophy-dystroglycanopathy type B6,,,,,,
+BMGC_DS22336,BMG_DS082879,,,,,,H18.50,DOID:0110855;DOID:0110857;DOID:0110856,posterior polymorphous corneal dystrophy 2 | posterior polymorphous corneal dystrophy 1 | posterior polymorphous corneal dystrophy 3,,,,,,
+BMGC_DS22337,BMG_DS083025,,,,AB51.1,Acquired sensorineural hearing loss,H90.3,DOID:0110544;DOID:0110572;DOID:0110556;DOID:0110589;DOID:0110479;DOID:0110489;DOID:0050566;DOID:0110480;DOID:0110584;DOID:0110514;DOID:0110472;DOID:0110523;DOID:0110580;DOID:0110465;DOID:0110543;DOID:0110588;DOID:0110583;DOID:0110515;DOID:0110478;DOID:0110527;DOID:0110564;DOID:0110492;DOID:0110560;DOID:0110558;DOID:0110522;DOID:0110503;DOID:0110476;DOID:0110474;DOID:0110497;DOID:0110568;DOID:0110567;DOID:0110469;DOID:0110512;DOID:0110576;DOID:0110506;DOID:0110557;DOID:0110486;DOID:0110545;DOID:0110586;DOID:0110463;DOID:0110585;DOID:0110490;DOID:0110575;DOID:0110541;DOID:0110561;DOID:0110504;DOID:0110593;DOID:0110547;DOID:0110498;DOID:0110555;DOID:0110482;DOID:0110562;DOID:0110571;DOID:0110511;DOID:0110590;DOID:0110496;DOID:0110536;DOID:0110513;DOID:0110552;DOID:0110495;DOID:0110499;DOID:0110484;DOID:0110530;DOID:0110534;DOID:0110501;DOID:0110546;DOID:0110565;DOID:0110467;DOID:0110475;DOID:0110526;DOID:0110579;DOID:0050564;DOID:0110468;DOID:0110507;DOID:0110563;DOID:0110540;DOID:0110508;DOID:0110505;DOID:0110577;DOID:0110477;DOID:0110587;DOID:0110566;DOID:0110471;DOID:0110531;DOID:0110488;DOID:0110569;DOID:0110535;DOID:0110473;DOID:0110559;DOID:0110592;DOID:0110516;DOID:0110582;DOID:0110533;DOID:0110493;DOID:0110553;DOID:0110581;DOID:0110470;DOID:0110520;DOID:0110481;DOID:0110537;DOID:0110548;DOID:0110510;DOID:0110485;DOID:0110519;DOID:0110464;DOID:0110525;DOID:0110549;DOID:0060690;DOID:0110509;DOID:0110538;DOID:0110462;DOID:0110487;DOID:0110529;DOID:0110573;DOID:0110554;DOID:0110494;DOID:0110517;DOID:0110491;DOID:0110521;DOID:0110539;DOID:0110551;DOID:0110542;DOID:0110570;DOID:0110574;DOID:0050565;DOID:0110591;DOID:0110500;DOID:0110518;DOID:0110483;DOID:0110502;DOID:0110550;DOID:0110524;DOID:0110528;DOID:0110532,autosomal recessive nonsyndromic deafness 48 | autosomal dominant nonsyndromic deafness 65 | autosomal recessive nonsyndromic deafness 68 | autosomal recessive nonsyndromic deafness 47 | autosomal recessive nonsyndromic deafness 1B | autosomal dominant nonsyndromic deafness 23 | autosomal recessive nonsyndromic deafness 7 | autosomal dominant nonsyndromic deafness 50 | autosomal dominant nonsyndromic deafness 69 | autosomal recessive nonsyndromic deafness 30 | autosomal recessive nonsyndromic deafness 61 | autosomal dominant nonsyndromic deafness 66 | autosomal dominant nonsyndromic deafness 16 | autosomal recessive nonsyndromic deafness 8 | autosomal recessive nonsyndromic deafness 77 | autosomal recessive nonsyndromic deafness 53 | autosomal recessive nonsyndromic deafness 84A | autosomal recessive nonsyndromic deafness 17 | autosomal dominant auditory neuropathy 1 | autosomal recessive nonsyndromic deafness 62 | autosomal recessive nonsyndromic deafness 63 | autosomal recessive nonsyndromic deafness 65 | autosomal recessive nonsyndromic deafness 59 | autosomal recessive nonsyndromic deafness 46 | autosomal dominant nonsyndromic deafness 48 | autosomal recessive nonsyndromic deafness | autosomal recessive nonsyndromic deafness 31 | autosomal recessive nonsyndromic deafness 26 | autosomal recessive nonsyndromic deafness 14 | autosomal recessive nonsyndromic deafness 2 | autosomal dominant nonsyndromic deafness 25 | autosomal recessive nonsyndromic deafness 102 | autosomal recessive nonsyndromic deafness 71 | autosomal recessive nonsyndromic deafness 18B | autosomal recessive nonsyndromic deafness 4 | autosomal dominant nonsyndromic deafness 28 | autosomal dominant nonsyndromic deafness 30 | autosomal dominant nonsyndromic deafness 4B | autosomal dominant nonsyndromic deafness 15 | autosomal recessive nonsyndromic deafness 85 | autosomal dominant nonsyndromic deafness 41 | autosomal recessive nonsyndromic deafness 33 | autosomal dominant nonsyndromic deafness 53 | autosomal dominant nonsyndromic deafness 67 | autosomal dominant nonsyndromic deafness 36 | autosomal dominant nonsyndromic deafness 68 | autosomal dominant nonsyndromic deafness | autosomal dominant nonsyndromic deafness 6 | autosomal recessive nonsyndromic deafness 25 | autosomal dominant nonsyndromic deafness 18 | autosomal dominant nonsyndromic deafness 33 | autosomal dominant nonsyndromic deafness 70 | autosomal dominant nonsyndromic deafness 56 | autosomal dominant nonsyndromic deafness 31 | autosomal recessive nonsyndromic deafness 98 | autosomal dominant nonsyndromic deafness 54 | autosomal recessive nonsyndromic deafness 16 | autosomal recessive nonsyndromic deafness 1A | autosomal recessive nonsyndromic deafness 22 | autosomal dominant nonsyndromic deafness 11 | autosomal recessive nonsyndromic deafness 9 | autosomal recessive nonsyndromic deafness 35 | autosomal recessive nonsyndromic deafness 21 | autosomal recessive nonsyndromic deafness 37 | autosomal dominant nonsyndromic deafness 12 | autosomal recessive nonsyndromic deafness 28 | autosomal recessive nonsyndromic deafness 101 | autosomal recessive nonsyndromic deafness 39 | autosomal recessive nonsyndromic deafness 91 | autosomal recessive nonsyndromic deafness 15 | autosomal recessive nonsyndromic deafness 84B | autosomal recessive nonsyndromic deafness 74 | autosomal recessive nonsyndromic deafness 93 | autosomal dominant nonsyndromic deafness 44 | autosomal recessive nonsyndromic deafness 96 | autosomal dominant nonsyndromic deafness 51 | autosomal recessive nonsyndromic deafness 38 | autosomal recessive nonsyndromic deafness 83 | autosomal dominant nonsyndromic deafness 58 | autosomal recessive nonsyndromic deafness 40 | autosomal recessive nonsyndromic deafness 51 | autosomal dominant nonsyndromic deafness 3B | autosomal dominant nonsyndromic deafness 24 | autosomal recessive nonsyndromic deafness 29 | autosomal recessive nonsyndromic deafness 55 | autosomal recessive nonsyndromic deafness 20 | autosomal recessive nonsyndromic deafness 13 | autosomal dominant nonsyndromic deafness 7 | autosomal recessive nonsyndromic deafness 32 | autosomal recessive nonsyndromic deafness 42 | autosomal recessive nonsyndromic deafness 5 | autosomal dominant nonsyndromic deafness 49 | autosomal dominant nonsyndromic deafness 21 | autosomal dominant nonsyndromic deafness 17 | autosomal recessive nonsyndromic deafness 104 | autosomal dominant nonsyndromic deafness 22 | autosomal recessive nonsyndromic deafness 97 | autosomal recessive nonsyndromic deafness 49 | autosomal dominant nonsyndromic deafness 59 | autosomal dominant nonsyndromic deafness 2A | autosomal dominant nonsyndromic deafness 3A | autosomal recessive nonsyndromic deafness 67 | autosomal dominant nonsyndromic deafness 27 | autosomal dominant nonsyndromic deafness 43 | autosomal recessive nonsyndromic deafness 70 | autosomal dominant nonsyndromic deafness 13 | autosomal recessive nonsyndromic deafness 24 | autosomal recessive nonsyndromic deafness 36 | autosomal dominant nonsyndromic deafness 2B | autosomal dominant nonsyndromic deafness 40 | autosomal dominant nonsyndromic deafness 47 | autosomal recessive nonsyndromic deafness 66 | autosomal dominant nonsyndromic deafness 20 | X-linked nonsyndromic deafness | autosomal recessive nonsyndromic deafness 76 | autosomal recessive nonsyndromic deafness 88 | autosomal dominant nonsyndromic deafness 4A | autosomal recessive nonsyndromic deafness 23 | autosomal recessive nonsyndromic deafness 12 | autosomal recessive nonsyndromic deafness 6 | autosomal recessive nonsyndromic deafness 45 | autosomal recessive nonsyndromic deafness 86 | autosomal recessive nonsyndromic deafness 89 | autosomal dominant nonsyndromic deafness 64 | autosomal recessive nonsyndromic deafness 103 | autosomal dominant nonsyndromic deafness 9 | autosomal recessive nonsyndromic deafness 79 | autosomal dominant nonsyndromic deafness 1 | autosomal dominant nonsyndromic deafness 5 | autosomal recessive nonsyndromic deafness 18A | autosomal recessive nonsyndromic deafness 27 | autosomal recessive nonsyndromic deafness 3 | autosomal recessive nonsyndromic deafness 44 | autosomal dominant nonsyndromic deafness 10,,,,,,
+BMGC_DS22338,BMG_DS083051,,,,BA02/GB6Z,,I12.0,,,,,,,,
+BMGC_DS22339,BMG_DS083109,,,,BC43.0Z,"Dilated cardiomyopathy, unspecified",I42.0,DOID:0110433;DOID:0110432;DOID:0110434;DOID:0110423;DOID:0110424;DOID:0110457;DOID:0110460;DOID:0110450;DOID:0110454;DOID:0110449;DOID:0110452;DOID:0110430;DOID:0110456;DOID:0110431;DOID:0110435;DOID:0110438;DOID:0110436;DOID:0110459;DOID:0110427;DOID:0110446;DOID:0110453;DOID:0110441;DOID:0110448;DOID:0110439;DOID:0110455;DOID:0110437;DOID:0110429;DOID:0110442;DOID:0110451;DOID:0110428;DOID:0110444;DOID:0110443;DOID:0110458;DOID:0110445;DOID:0110447;DOID:0110426,dilated cardiomyopathy 2B | dilated cardiomyopathy 1FF | dilated cardiomyopathy 1S | dilated cardiomyopathy 1L | dilated cardiomyopathy 1C | dilated cardiomyopathy 1JJ | dilated cardiomyopathy 1Q | dilated cardiomyopathy 1CC | dilated cardiomyopathy 1DD | dilated cardiomyopathy 1NN | dilated cardiomyopathy 1Z | dilated cardiomyopathy 1V | dilated cardiomyopathy 1T | dilated cardiomyopathy 1I | dilated cardiomyopathy 1H | dilated cardiomyopathy 1R | dilated cardiomyopathy 1W | dilated cardiomyopathy 1II | dilated cardiomyopathy 1HH | dilated cardiomyopathy 1GG | dilated cardiomyopathy 1B | dilated cardiomyopathy 1P | dilated cardiomyopathy 1KK | dilated cardiomyopathy 1X | dilated cardiomyopathy 1M | dilated cardiomyopathy 1E | dilated cardiomyopathy 1EE | dilated cardiomyopathy 2A | dilated cardiomyopathy 1BB | dilated cardiomyopathy 1Y | dilated cardiomyopathy 1O | dilated cardiomyopathy 1AA | dilated cardiomyopathy 1K | dilated cardiomyopathy 1D | dilated cardiomyopathy 1U | dilated cardiomyopathy 1G,,,,,,
+BMGC_DS22340,BMG_DS083114,,,,,,I42.8;I47.2,DOID:0060675,catecholaminergic polymorphic ventricular tachycardia 1,,,,,,
+BMGC_DS22341,BMG_DS083128,,,,BC63.Z,"Conduction disorders, unspecified",I45.8,DOID:0110644;DOID:0110655;DOID:0110654;DOID:0110656,long QT syndrome 14 | long QT syndrome 1 | long QT syndrome 13 | long QT syndrome 15,,,,,,
+BMGC_DS22342,BMG_DS083134,,,,BC71.0Z,"Ventricular tachycardia, unspecified",I47.2,DOID:0060677;DOID:0060678;DOID:0060676;DOID:0060674;DOID:0060679,catecholaminergic polymorphic ventricular tachycardia 2 | catecholaminergic polymorphic ventricular tachycardia 5 | catecholaminergic polymorphic ventricular tachycardia | catecholaminergic polymorphic ventricular tachycardia 3 | catecholaminergic polymorphic ventricular tachycardia 4,,,,,,
+BMGC_DS22343,BMG_DS083234,,,,DB98.5,BuddChiari syndrome,I82.0,,,,,,,,
+BMGC_DS22344,BMG_DS083257,,,,DA26.00/DB96.0,,I98.3,,,,,,,,
+BMGC_DS22345,BMG_DS083312,,,,CA23.0,Allergic asthma,J45.0,,,,,,,,
+BMGC_DS22346,BMG_DS083314,,,,CA23,Asthma,J45.8,,,,,,,,
+BMGC_DS22347,BMG_DS083341,,,,CB05.1/FA20.Z,,J99.0,,,,,,,,
+BMGC_DS22348,BMG_DS083347,,,,LA30.Z,"Structural developmental anomalies of teeth and periodontal tissues, unspecified",K00.5,DOID:0110061;DOID:0110065;DOID:0110053;DOID:0110054;DOID:0110057;DOID:0110060;DOID:0110056;DOID:0110062;DOID:0110064;DOID:0110063;DOID:0110066;DOID:0110059;DOID:0110055;DOID:0110052;DOID:0110058,amelogenesis imperfecta type 1B | amelogenesis imperfecta type 1G | amelogenesis imperfecta type 4 | amelogenesis imperfecta type 1A | amelogenesis imperfecta type 1C | amelogenesis imperfecta type 1E | amelogenesis imperfecta type 1F | amelogenesis imperfecta type 2A1 | amelogenesis imperfecta hypomaturation type 2A3 | amelogenesis imperfecta hypomaturation type 2A2 | amelogenesis imperfecta type 1H | amelogenesis imperfecta hypomaturation type 2A4 | amelogenesis imperfecta hypomaturation type 2A5 | amelogenesis imperfecta type 3A | X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2,,,,,,
+BMGC_DS22349,BMG_DS083410,,,,DA23.Z,"Columnar metaplastic epithelium of the oesophagus, unspecified",K22.7,,,,,,,,
+BMGC_DS22350,BMG_DS083412,,,,1B12.7/DA24.0Y,,K23.0,,,,,,,,
+BMGC_DS22351,BMG_DS083414,,,,XA0828/DA21.Y,,K23.1,,,,,,,,
+BMGC_DS22352,BMG_DS083456,,,,XK9J/ME24.2,,K40.0,,,,,,,,
+BMGC_DS22353,BMG_DS083458,,,,XK9J/ME24.8,,K40.1,,,,,,,,
+BMGC_DS22354,BMG_DS083461,,,,DD51/ME24.2,,K40.3,,,,,,,,
+BMGC_DS22355,BMG_DS083462,,,,DD51/ME24.8,,K40.4,,,,,,,,
+BMGC_DS22356,BMG_DS083465,,,,XK9J/ME24.2,,K41.0,,,,,,,,
+BMGC_DS22357,BMG_DS083468,,,,XT44/ME24.8,,K41.1,,,,,,,,
+BMGC_DS22358,BMG_DS083471,,,,DD52/ME24.2,,K41.3,,,,,,,,
+BMGC_DS22359,BMG_DS083472,,,,DD52/ME24.8,,K41.4,,,,,,,,
+BMGC_DS22360,BMG_DS083474,,,,DD53/ME24.2,,K42.0,,,,,,,,
+BMGC_DS22361,BMG_DS083476,,,,DD56/ME24.2,,K43.0,,,,,,,,
+BMGC_DS22362,BMG_DS083478,,,,DD57/ME24.2,,K43.3,,,,,,,,
+BMGC_DS22363,BMG_DS083483,,,,DD50.0/ME24.2,,K44.0,,,,,,,,
+BMGC_DS22364,BMG_DS083498,,,,DE2Z,"Diseases of the digestive system, unspecified",K59.0,,,,,,,,
+BMGC_DS22365,BMG_DS083593,,,,1F53.3/DB32.2Z,,K93.1,,,,,,,,
+BMGC_DS22366,BMG_DS083619,,,,EK00.6,Allergic contact dermatitis due to metals or metal salts,L23.0,DOID:0040056;DOID:0040046,chromium allergic contact dermatitis | nickel allergic contact dermatitis,,,,,,
+BMGC_DS22367,BMG_DS083657,,,,EA90.42,Palmoplantar pustulosis,L40.3,,,,,,,,
+BMGC_DS22368,BMG_DS083658,,,,EA90.1,Guttate psoriasis,L40.4,,,,,,,,
+BMGC_DS22369,BMG_DS083669,,,,,,L50.2,DOID:0090061;DOID:0090065;DOID:0090062;DOID:0090064,familial cold autoinflammatory syndrome 4 | familial cold autoinflammatory syndrome | familial cold autoinflammatory syndrome 3 | familial cold autoinflammatory syndrome 1,,,,,,
+BMGC_DS22370,BMG_DS083779,,,,1B12.40/FA10.0,,M01.1,,,,,,,,
+BMGC_DS22371,BMG_DS083796,,,,CB05.1/FA20.Z,,M05.1,,,,,,,,
+BMGC_DS22372,BMG_DS083807,,,,FA11.Y/DD70.Z,,M07.4,,,,,,,,
+BMGC_DS22373,BMG_DS083808,,,,FA11.Y/DD71.Z,,M07.5,,,,,,,,
+BMGC_DS22374,BMG_DS083812,,,,FA24.2,Juvenile psoriatic arthritis,M09.0,,,,,,,,
+BMGC_DS22375,BMG_DS083813,,,,FA11.Y/DD70.Z,,M09.1,,,,,,,,
+BMGC_DS22376,BMG_DS083831,,,,5D00.0/FA38.Z,,M14.4,,,,,,,,
+BMGC_DS22377,BMG_DS083857,,,,FA31.Z,"Acquired deformities of limbs, unspecified",M21.8,DOID:0060231,Bruck syndrome,,,,,,
+BMGC_DS22378,BMG_DS083897,,,,,,M32.11,DOID:0080740,Libman-Sacks endocarditis,,,,,,
+BMGC_DS22379,BMG_DS083903,,,,4A43.Z,Undifferentiated nonorgan specific systemic autoimmune disease,M35.0,,,,,,,,
+BMGC_DS22380,BMG_DS083993,,,,1A62.21/FB50.0,,M73.1,,,,,,,,
+BMGC_DS22381,BMG_DS084120,,,,XT8W/MF8Y,,N03.2,,,,,,,,
+BMGC_DS22382,BMG_DS084122,,,,XT8W/MF8Y,,N03.3,,,,,,,,
+BMGC_DS22383,BMG_DS084124,,,,XT8W/MF8Y,,N03.4,,,,,,,,
+BMGC_DS22384,BMG_DS084185,,,,GC01.4,"Neuromuscular dysfunction of bladder, not elsewhere classified",N31.0,,,,,,,,
+BMGC_DS22385,BMG_DS084239,,,,1B12.5/GA04,,N74.0,,,,,,,,
+BMGC_DS22386,BMG_DS084242,,,,1A71/GA05.Z,,N74.3,,,,,,,,
+BMGC_DS22387,BMG_DS084243,,,,1A81.1/GA05.Z,,N74.4,,,,,,,,
+BMGC_DS22388,BMG_DS084465,,,,JA65.10,Gestational pemphigoid,O26.4,DOID:0040098,pemphigus gestationis,,,,,,
+BMGC_DS22389,BMG_DS085000,,,,LA05.Z,"Cerebral structural developmental anomalies, unspecified",Q04.3,DOID:0110096;DOID:0060807;DOID:0060277;DOID:0060270;DOID:0060278;DOID:0090137;DOID:0060276;DOID:0050777,short-rib thoracic dysplasia 14 with polydactyly | pontocerebellar hypoplasia type 7 | pontocerebellar hypoplasia type 9 | pontocerebellar hypoplasia type 2D | complex cortical dysplasia with other brain malformations 1 | syndromic X-linked intellectual disability Najm type | Joubert syndrome | pontocerebellar hypoplasia type 8,,,,,,
+BMGC_DS22390,BMG_DS085036,,,,LA12.1,Congenital cataract,Q12.0,DOID:0110245;DOID:0110261;DOID:0110237;DOID:0110235;DOID:0110271;DOID:0110239;DOID:0110272;DOID:0110270;DOID:0110236;DOID:0110249;DOID:0110229;DOID:0110246;DOID:0110251;DOID:0110263;DOID:0110253;DOID:0110227;DOID:0110267;DOID:0110257;DOID:0110256;DOID:0110234;DOID:0110254;DOID:0110241;DOID:0110268;DOID:0110250;DOID:0110231;DOID:0110260;DOID:0110242;DOID:0110266;DOID:0110265;DOID:0110240;DOID:0110230;DOID:0110262;DOID:0110258;DOID:0110259;DOID:0110269;DOID:0110243;DOID:0110248;DOID:0110233;DOID:0110228;DOID:0110232;DOID:0110238;DOID:0110255;DOID:0110252;DOID:0110264,cataract 9 multiple types | cataract 42 | cataract 39 multiple types | cataract 29 | cataract 43 | cataract 45 | cataract 38 | cataract 2 multiple types | cataract 23 | cataract 22 multiple types | cataract 20 multiple types | cataract 35 | cataract 5 multiple types | cataract 14 multiple types | cataract 37 | cataract 17 multiple types | cataract 21 multiple types | cataract 34 multiple types | cataract 41 | cataract 12 multiple types | cataract 31 multiple types | cataract 32 multiple types | cataract 3 multiple types | cataract 18 | cataract 6 multiple types | cataract 16 multiple types | cataract 10 multiple types | cataract 19 multiple types | cataract 46 juvenile-onset | cataract 26 multiple types | cataract 24 | cataract 40 | cataract 7 | cataract 25 | cataract 11 multiple types | cataract 1 multiple types | cataract 30 | cataract 8 multiple types | cataract 27 | cataract 33 | cataract 15 multiple types | cataract 13 with adult i phenotype | cataract 4 multiple types | cataract 44,,,,,,
+BMGC_DS22391,BMG_DS085047,,,,LA11.Z,"Structural developmental anomalies of the anterior segment of eye, unspecified",Q13.4,DOID:0060287,cornea plana,,,,,,
+BMGC_DS22392,BMG_DS085049,,,,LA11.Z,"Structural developmental anomalies of the anterior segment of eye, unspecified",Q13.8,DOID:0060648;DOID:0110122;DOID:0110121;DOID:0110120,Axenfeld-Rieger syndrome type 1 | Axenfeld-Rieger syndrome type 2 | anterior segment dysgenesis | Axenfeld-Rieger syndrome type 3,,,,,,
+BMGC_DS22393,BMG_DS085052,,,,LA13.3,Congenital vitreoretinal dysplasia,Q14.1,DOID:0060763,X-linked juvenile retinoschisis 1,,,,,,
+BMGC_DS22394,BMG_DS085087,,,,LA85.1,Transposition of the great arteries,Q20.3,DOID:0060772;DOID:0060770,multiple types of congenital heart defects 6 | dextro-looped transposition of the great arteries,,,,,,
+BMGC_DS22395,BMG_DS085090,,,,LA8Y,Other specified structural developmental anomaly of heart or great vessels,Q20.6,DOID:0060856,right atrial isomerism,,,,,,
+BMGC_DS22396,BMG_DS085094,,,,LA8E.Z,"Congenital anomaly of atrial septum, unspecified",Q21.1,DOID:0110113;DOID:0110114;DOID:0110109;DOID:0110112;DOID:0110110;DOID:0110108;DOID:0110111;DOID:0110107;DOID:0110106,atrial heart septal defect 8 | atrial heart septal defect 1 | atrial heart septal defect 6 | atrial heart septal defect 3 | atrial heart septal defect 2 | atrial heart septal defect 9 | atrial heart septal defect 7 | atrial heart septal defect 4 | atrial heart septal defect 5,,,,,,
+BMGC_DS22397,BMG_DS085178,,,,LA7Z,"Structural developmental anomalies of the respiratory system, unspecified",Q34.8,DOID:0110604;DOID:0110607;DOID:0110624;DOID:0110611;DOID:0110594;DOID:0110598;DOID:0110614;DOID:0110608;DOID:0110606;DOID:0110602;DOID:0110627;DOID:0110600;DOID:0110622;DOID:0110601;DOID:0110625;DOID:0110615;DOID:0110623;DOID:0110626;DOID:0110619;DOID:0110597;DOID:0110613;DOID:0110616;DOID:0110605;DOID:0110628;DOID:0110621;DOID:0110612;DOID:0110596;DOID:0110618;DOID:0110603;DOID:0110609;DOID:0110599;DOID:0110617,primary ciliary dyskinesia 22 | primary ciliary dyskinesia 13 | primary ciliary dyskinesia 16 | primary ciliary dyskinesia 23 | primary ciliary dyskinesia 15 | primary ciliary dyskinesia 24 | primary ciliary dyskinesia 8 | primary ciliary dyskinesia 33 | primary ciliary dyskinesia 14 | primary ciliary dyskinesia 11 | primary ciliary dyskinesia 17 | primary ciliary dyskinesia 18 | primary ciliary dyskinesia 19 | primary ciliary dyskinesia 27 | primary ciliary dyskinesia 30 | primary ciliary dyskinesia 7 | primary ciliary dyskinesia 10 | primary ciliary dyskinesia 4 | primary ciliary dyskinesia 5 | primary ciliary dyskinesia 20 | primary ciliary dyskinesia 12 | primary ciliary dyskinesia 3 | primary ciliary dyskinesia 1 | primary ciliary dyskinesia 28 | primary ciliary dyskinesia 6 | primary ciliary dyskinesia 2 | primary ciliary dyskinesia 25 | primary ciliary dyskinesia 9 | primary ciliary dyskinesia 21 | primary ciliary dyskinesia 29 | primary ciliary dyskinesia 32 | primary ciliary dyskinesia 26,,,,,,
+BMGC_DS22398,BMG_DS085181,,,,,,Q35.1;Q35.3;Q35.5;Q35.7;Q35.9,DOID:0110213,isolated cleft palate,,,,,,
+BMGC_DS22399,BMG_DS085233,,,,LB16.1,Hirschsprung disease,Q43.1,,,,,,,,
+BMGC_DS22400,BMG_DS085243,,,,LB20.21,Biliary atresia,Q44.2,,,,,,,,
+BMGC_DS22401,BMG_DS085264,,,,LB44.3,Bicornuate uterus,Q51.2,DOID:0060739,hand-foot-genital syndrome,,,,,,
+BMGC_DS22402,BMG_DS085308,,,,LB30.0Y,Other specified renal agenesis or other reduction defects of kidney,Q60.4,DOID:0111142;DOID:0090006,renal coloboma syndrome | oligomeganephronia,,,,,,
+BMGC_DS22403,BMG_DS085372,,,,LD0Z,"Structural developmental anomalies primarily affecting one body system, unspecified",Q68.8,DOID:0060558,lethal congenital contracture syndrome,,,,,,
+BMGC_DS22404,BMG_DS085389,,,,LB99.8,Split hand,Q71.6,DOID:0090021,split hand-foot malformation 1,,,,,,
+BMGC_DS22405,BMG_DS085419,,,,LB73.25,Congenital scoliosis due to congenital bony malformation,Q76.3,DOID:0090143,brachyolmia-amelogenesis imperfecta syndrome,,,,,,
+BMGC_DS22406,BMG_DS085420,,,,LB73.2Z,"Structural developmental anomalies of spine, unspecified",Q76.4,DOID:0090116,spondylocarpotarsal synostosis syndrome,,,,,,
+BMGC_DS22407,BMG_DS085428,,,,,,Q77.2;Q87.5,DOID:0110091,short-rib thoracic dysplasia 10 with or without polydactyly,,,,,,
+BMGC_DS22408,BMG_DS085429,,,,LD24.04,Chondrodysplasia punctata,Q77.3,DOID:0110851;DOID:0060293,autosomal dominant chondrodysplasia punctata | rhizomelic chondrodysplasia punctata type 1,,,,,,
+BMGC_DS22409,BMG_DS085432,,,,LD24.3,Spondyloepiphyseal or spondyloepimetaphyseal dysplasias,Q77.7,DOID:0090032;DOID:0090004,progressive pseudorheumatoid arthropathy of childhood | Silverman-Handmaker type dyssegmental dysplasia,,,,,,
+BMGC_DS22410,BMG_DS085435,,,,LD24.K0,Osteogenesis imperfecta,Q78.0,DOID:0110344;DOID:0110338;DOID:0110336;DOID:0110346;DOID:0110340;DOID:0110342;DOID:0110335;DOID:0110348;DOID:0110343;DOID:0110339;DOID:0110341;DOID:0110345;DOID:0110349;DOID:0110351;DOID:0110350;DOID:0110347,"osteogenesis imperfecta type 2 | osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures | osteogenesis imperfecta type 11 | osteogenesis imperfecta type 6 | osteogenesis imperfecta type 13 | osteogenesis imperfecta type 5 | osteogenesis imperfecta type 9 | osteogenesis imperfecta type 10 | osteogenesis imperfecta type 4 | osteogenesis imperfecta type 8 | osteogenesis imperfecta type 17 | osteogenesis imperfecta type 3 | osteogenesis imperfecta type 14 | osteogenesis imperfecta type 16 | osteogenesis imperfecta type 12 | osteogenesis imperfecta type 15",,,,,,
+BMGC_DS22411,BMG_DS085451,,,,EC20.02,Autosomal recessive congenital ichthyosis,Q80.2,DOID:0060710;DOID:0060716;DOID:0060717;DOID:0060719;DOID:0060715;DOID:0060656;DOID:0060711;DOID:0060714;DOID:0060718;DOID:0060712,autosomal recessive congenital ichthyosis 1 | autosomal recessive congenital ichthyosis 5 | autosomal recessive congenital ichthyosis 2 | autosomal recessive congenital ichthyosis 7 | autosomal recessive congenital ichthyosis 4A | autosomal recessive congenital ichthyosis 6 | autosomal recessive congenital ichthyosis 3 | autosomal recessive congenital ichthyosis 8 | autosomal recessive congenital ichthyosis 10 | autosomal recessive congenital ichthyosis 9,,,,,,
+BMGC_DS22412,BMG_DS085453,,,,EC20.02,Autosomal recessive congenital ichthyosis,Q80.4,DOID:0060713,autosomal recessive congenital ichthyosis 4B,,,,,,
+BMGC_DS22413,BMG_DS085455,,,,EC30,Epidermolysis bullosa simplex,Q81.0,DOID:0060735;DOID:0060736;DOID:0090017,epidermolysis bullosa simplex Dowling-Meara type | epidermolysis bullosa simplex Ogna type | epidermolysis bullosa simplex with muscular dystrophy,,,,,,
+BMGC_DS22414,BMG_DS085456,,,,EC31,Junctional epidermolysis bullosa,Q81.1,DOID:0060737,junctional epidermolysis bullosa Herlitz type,,,,,,
+BMGC_DS22415,BMG_DS085457,,,,EC32,Dystrophic epidermolysis bullosa,Q81.2,DOID:0060642,recessive dystrophic epidermolysis bullosa,,,,,,
+BMGC_DS22416,BMG_DS085458,,,,EC3Z,Epidermolysis bullosa,Q81.8,DOID:0060738;DOID:0060733,junctional epidermolysis bullosa with pyloric atresia | junctional epidermolysis bullosa non-Herlitz type,,,,,,
+BMGC_DS22417,BMG_DS085460,,,,LD27.1,Xeroderma pigmentosum,Q82.1,DOID:0110844;DOID:0110850;DOID:0110845;DOID:0110849;DOID:0110848;DOID:0110846;DOID:0110843,xeroderma pigmentosum group E | xeroderma pigmentosum group D | xeroderma pigmentosum group G | xeroderma pigmentosum group A | xeroderma pigmentosum group F | xeroderma pigmentosum group C | xeroderma pigmentosum group B,,,,,,
+BMGC_DS22418,BMG_DS085483,,,,LD2Z,"Multiple developmental anomalies or syndromes, unspecified",Q87.1,DOID:0060578;DOID:0050569;DOID:0060588;DOID:0060587;DOID:0060585;DOID:0060586,Noonan syndrome 10 | Noonan syndrome 1 | Noonan syndrome 9 | Noonan syndrome 8 | Noonan syndrome 7 | Seckel syndrome,,,,,,
+BMGC_DS22419,BMG_DS085485,,,,LD2Z,"Multiple developmental anomalies or syndromes, unspecified",Q87.8,DOID:0060824;DOID:0050764;DOID:0060830;DOID:0060816;DOID:0060813;DOID:0060804;DOID:0110595;DOID:0060820;DOID:0060822;DOID:0060811;DOID:0060809;DOID:0060641;DOID:0060747;DOID:0060225;DOID:0060826;DOID:0060802,"endocrine-cerebro-osteodysplasia syndrome | deafness-intellectual disability, Martin-Probst type syndrome | Duane-radial ray syndrome | syndromic X-linked intellectual disability Nascimento type | syndromic X-linked intellectual disability Cabezas type | syndromic X-linked intellectual disability Claes-Jensen type | syndromic X-linked intellectual disability Turner type | syndromic X-linked intellectual disability Raymond type | Stromme syndrome | Armfield syndrome | syndromic X-linked intellectual disability Shrimpton type | syndromic X-linked intellectual disability Snyder type | syndromic X-linked intellectual disability 12 | syndromic X-linked intellectual disability Shashi type | 3MC syndrome | corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome",,,,,,
+BMGC_DS22420,BMG_DS085486,,,,,,Q87.89,DOID:0110141;DOID:0110137;DOID:0110138;DOID:0110140;DOID:0110139;DOID:0110127,Bardet-Biedl syndrome 16 | Bardet-Biedl syndrome 18 | Bardet-Biedl syndrome 19 | Bardet-Biedl syndrome 17 | Bardet-Biedl syndrome 5 | Bardet-Biedl syndrome 15,,,,,,
+BMGC_DS22421,BMG_DS085515,,,,LD44.Z,"Deletions of the autosomes, unspecified",Q93.5,DOID:0060411;DOID:0060391;DOID:0060400;DOID:0060425;DOID:0060417;DOID:0060412;DOID:0060405;DOID:0060404,chromosome 13q14 deletion syndrome | chromosome 17q23.1-q23.2 deletion syndrome | chromosome 17q12 deletion syndrome | chromosome 8q21.11 deletion syndrome | chromosome 1q21.1 deletion syndrome | chromosome 16p12.2-p11.2 deletion syndrome | chromosome 1q41-q42 deletion syndrome | 3p deletion syndrome,,,,,,
+BMGC_DS22422,BMG_DS085588,,,,MD94,Halitosis,R19.6,,,,,,,,
+BMGC_DS22423,BMG_DS085718,,,,MA18.0Z,"Elevated blood glucose level, unspecified",R73.9,,,,,,,,
+BMGC_DS22424,BMG_DS086495,,,,ND51.Z,"Unspecified injuries of spine or trunk, level unspecified",T09.3,,,,,,,,
+BMGC_DS22425,BMG_DS086961,,,,4A8Z,Allergic or hypersensitivity conditions of unspecified type,T78.4,,,,,,,,
+BMGC_DS22426,BMG_DS091971,,,,5B81,Obesity,,,,,,,,,
+BMGC_DS22427,BMG_DS094697,,,,CA25,Cystic fibrosis,,,,,,,,,
+BMGC_DS22428,BMG_DS095586,,,,EA90,Psoriasis,,,,,,,,,
+BMGC_DS22429,BMG_DS118713,,,,XS8H,,,,,,,,,,