diff --git "a/BioMedGraphica-Conn/Entity/Disease/BioMedGraphica_Conn_Disease_Display_Name.csv" "b/BioMedGraphica-Conn/Entity/Disease/BioMedGraphica_Conn_Disease_Display_Name.csv"
new file mode 100644--- /dev/null
+++ "b/BioMedGraphica-Conn/Entity/Disease/BioMedGraphica_Conn_Disease_Display_Name.csv"
@@ -0,0 +1,22430 @@
+BioMedGraphica_Conn_ID,BioMedGraphica_ID,BMG_Disease_Name
+BMGC_DS00001,BMG_DS000001,Abetalipoproteinemia
+BMGC_DS00002,BMG_DS000002,Abnormality of secretion of gastrin
+BMGC_DS00003,BMG_DS000003,"Abortion, Habitual"
+BMGC_DS00004,BMG_DS000004,Missed abortion
+BMGC_DS00005,BMG_DS000005,placental abruption
+BMGC_DS00006,BMG_DS000006,"Abortion, Veterinary"
+BMGC_DS00007,BMG_DS000007,placental abruption
+BMGC_DS00008,BMG_DS000008,Abscess
+BMGC_DS00009,BMG_DS000009,Acanthamoeba Keratitis
+BMGC_DS00010,BMG_DS000010,Acanthosis Nigricans
+BMGC_DS00011,BMG_DS000011,achlorhydria
+BMGC_DS00012,BMG_DS000012,achondrogenesis
+BMGC_DS00013,BMG_DS000013,Achondroplasia
+BMGC_DS00014,BMG_DS000014,acidosis disorder
+BMGC_DS00015,BMG_DS000015,"Acidosis, Lactic"
+BMGC_DS00016,BMG_DS000016,Renal tubular acidosis
+BMGC_DS00017,BMG_DS000017,"Acidosis, Respiratory"
+BMGC_DS00018,BMG_DS000018,Acinetobacter Infections
+BMGC_DS00019,BMG_DS000020,Acne Vulgaris
+BMGC_DS00020,BMG_DS000022,Vestibulocochlear Nerve Diseases
+BMGC_DS00021,BMG_DS000024,Acquired Immunodeficiency Syndrome
+BMGC_DS00022,BMG_DS000025,Apert syndrome
+BMGC_DS00023,BMG_DS000026,Acrodermatitis
+BMGC_DS00024,BMG_DS000028,Acromegaly
+BMGC_DS00025,BMG_DS000029,Hypersomatotropic gigantism
+BMGC_DS00026,BMG_DS000030,"ACTH Syndrome, Ectopic"
+BMGC_DS00027,BMG_DS000034,Actinomycosis
+BMGC_DS00028,BMG_DS000035,Abdominal actinomycosis
+BMGC_DS00029,BMG_DS000036,Cervicofacial actinomycosis
+BMGC_DS00030,BMG_DS000039,Acute alcoholic liver disease
+BMGC_DS00031,BMG_DS000040,Acute and subacute liver necrosis (disorder)
+BMGC_DS00032,BMG_DS000041,Acute atopic conjunctivitis
+BMGC_DS00033,BMG_DS000043,Acute Disease
+BMGC_DS00034,BMG_DS000044,Acute laryngitis
+BMGC_DS00035,BMG_DS000045,Herpetic Acute Necrotizing Encephalitis
+BMGC_DS00036,BMG_DS000046,"Pancreatitis, Acute"
+BMGC_DS00037,BMG_DS000047,Acute periodontitis
+BMGC_DS00038,BMG_DS000048,Acute pharyngitis
+BMGC_DS00039,BMG_DS000049,Acute thyroiditis
+BMGC_DS00040,BMG_DS000051,Acute vascular insufficiency of intestine (disorder)
+BMGC_DS00041,BMG_DS000053,Adams-Stokes Syndrome
+BMGC_DS00042,BMG_DS000054,Addison Disease
+BMGC_DS00043,BMG_DS000055,adenocarcinoma
+BMGC_DS00044,BMG_DS000056,papillary adenocarcinoma
+BMGC_DS00045,BMG_DS000057,adenofibroma
+BMGC_DS00046,BMG_DS000060,adenoma
+BMGC_DS00047,BMG_DS000061,pituitary gland basophil adenoma
+BMGC_DS00048,BMG_DS000062,chromophobe adenoma
+BMGC_DS00049,BMG_DS000063,pituitary gland acidophil adenoma
+BMGC_DS00050,BMG_DS000064,adenosarcoma
+BMGC_DS00051,BMG_DS000065,disease by infectious agent
+BMGC_DS00052,BMG_DS000068,Adie Syndrome
+BMGC_DS00053,BMG_DS000069,Adiposis Dolorosa
+BMGC_DS00054,BMG_DS000073,Adrenal Cortex Diseases
+BMGC_DS00055,BMG_DS000074,adrenal cortex neoplasm
+BMGC_DS00056,BMG_DS000075,Adrenal Gland Diseases
+BMGC_DS00057,BMG_DS000076,Adrenal Gland Hyperfunction
+BMGC_DS00058,BMG_DS000077,adrenal gland neoplasm
+BMGC_DS00059,BMG_DS000078,Congenital adrenal hyperplasia
+BMGC_DS00060,BMG_DS000081,Afferent Loop Syndrome
+BMGC_DS00061,BMG_DS000082,Afibrinogenemia
+BMGC_DS00062,BMG_DS000085,Agammaglobulinemia
+BMGC_DS00063,BMG_DS000086,"Osteoporosis, Age-Related"
+BMGC_DS00064,BMG_DS000087,primary myelofibrosis
+BMGC_DS00065,BMG_DS000088,agnosia
+BMGC_DS00066,BMG_DS000089,agoraphobia
+BMGC_DS00067,BMG_DS000090,Agranulocytosis
+BMGC_DS00068,BMG_DS000092,Agricultural Workers' Diseases
+BMGC_DS00069,BMG_DS000093,AIDS Dementia Complex
+BMGC_DS00070,BMG_DS000095,Ainhum
+BMGC_DS00071,BMG_DS000096,Airsickness
+BMGC_DS00072,BMG_DS000097,Airway Obstruction
+BMGC_DS00073,BMG_DS000098,Akinetic Mutism
+BMGC_DS00074,BMG_DS000099,Akinetic Petit Mal
+BMGC_DS00075,BMG_DS000100,Variola Minor
+BMGC_DS00076,BMG_DS000101,Albinism
+BMGC_DS00077,BMG_DS000103,Alcohol Withdrawal Delirium
+BMGC_DS00078,BMG_DS000104,alcohol dependence
+BMGC_DS00079,BMG_DS000105,Aleutian Mink Disease
+BMGC_DS00080,BMG_DS000106,alexia
+BMGC_DS00081,BMG_DS000107,alexithymia
+BMGC_DS00082,BMG_DS000108,Alkalosis
+BMGC_DS00083,BMG_DS000109,Alkaptonuria
+BMGC_DS00084,BMG_DS000111,Atopic rhinitis
+BMGC_DS00085,BMG_DS000114,Alopecia
+BMGC_DS00086,BMG_DS000115,Alopecia Areata
+BMGC_DS00087,BMG_DS000116,"Mucinosis, Follicular"
+BMGC_DS00088,BMG_DS000123,alpha-Thalassemia
+BMGC_DS00089,BMG_DS000124,Altitude Sickness
+BMGC_DS00090,BMG_DS000125,Alveolar Bone Loss
+BMGC_DS00091,BMG_DS000126,Extrinsic allergic alveolitis
+BMGC_DS00092,BMG_DS000127,Alzheimer's Disease
+BMGC_DS00093,BMG_DS000128,Amblyopia
+BMGC_DS00094,BMG_DS000129,Tobacco amblyopia
+BMGC_DS00095,BMG_DS000130,Amebiasis
+BMGC_DS00096,BMG_DS000134,ameloblastoma
+BMGC_DS00097,BMG_DS000135,amelogenesis imperfecta
+BMGC_DS00098,BMG_DS000136,amenorrhea
+BMGC_DS00099,BMG_DS000137,"Amino Acid Metabolism, Inborn Errors"
+BMGC_DS00100,BMG_DS000138,Renal Aminoacidurias
+BMGC_DS00101,BMG_DS000139,amnestic disorder
+BMGC_DS00102,BMG_DS000140,retrograde amnesia
+BMGC_DS00103,BMG_DS000141,amnestic disorder
+BMGC_DS00104,BMG_DS000142,Infection of amniotic cavity
+BMGC_DS00105,BMG_DS000145,Amyloidosis
+BMGC_DS00106,BMG_DS000146,Oppenheim's Disease
+BMGC_DS00107,BMG_DS000147,Amyotrophic Lateral Sclerosis
+BMGC_DS00108,BMG_DS000148,anal gland neoplasm
+BMGC_DS00109,BMG_DS000149,Congenital Pain Insensitivity
+BMGC_DS00110,BMG_DS000152,Ancylostomiasis
+BMGC_DS00111,BMG_DS000153,Anemia
+BMGC_DS00112,BMG_DS000155,Aplastic Anemia
+BMGC_DS00113,BMG_DS000156,Cooley's anemia
+BMGC_DS00114,BMG_DS000157,Congenital dyserythropoietic anemia
+BMGC_DS00115,BMG_DS000158,"Anemia, Hemolytic"
+BMGC_DS00116,BMG_DS000159,"Anemia, Hemolytic, Acquired"
+BMGC_DS00117,BMG_DS000160,Autoimmune hemolytic anemia
+BMGC_DS00118,BMG_DS000161,"Anemia, Hemolytic, Congenital"
+BMGC_DS00119,BMG_DS000162,"Anemia, Hemolytic, Congenital Nonspherocytic"
+BMGC_DS00120,BMG_DS000163,"Anemia, Hemolytic, Idiopathic Acquired"
+BMGC_DS00121,BMG_DS000164,Hypochromic anemia
+BMGC_DS00122,BMG_DS000165,"Anemia, Macrocytic"
+BMGC_DS00123,BMG_DS000166,"Anemia, Megaloblastic"
+BMGC_DS00124,BMG_DS000167,"Anemia, Microangiopathic"
+BMGC_DS00125,BMG_DS000168,Leukoerythroblastic Anemia
+BMGC_DS00126,BMG_DS000169,"Anemia, Neonatal"
+BMGC_DS00127,BMG_DS000170,"Anemia, Pernicious"
+BMGC_DS00128,BMG_DS000172,"Anemia, Sickle Cell"
+BMGC_DS00129,BMG_DS000173,Sideroblastic anemia
+BMGC_DS00130,BMG_DS000174,"Anemia, Splenic"
+BMGC_DS00131,BMG_DS000175,anencephaly
+BMGC_DS00132,BMG_DS000176,aneuploidy
+BMGC_DS00133,BMG_DS000177,vascular disease
+BMGC_DS00134,BMG_DS000178,Arterial Dissection
+BMGC_DS00135,BMG_DS000181,"Angina Pectoris, Variant"
+BMGC_DS00136,BMG_DS000182,"Angina, Unstable"
+BMGC_DS00137,BMG_DS000183,Angioid Streaks
+BMGC_DS00138,BMG_DS000184,Angioid streaks of choroid
+BMGC_DS00139,BMG_DS000185,angiokeratoma
+BMGC_DS00140,BMG_DS000186,Fabry Disease
+BMGC_DS00141,BMG_DS000187,skin epithelioid hemangioma
+BMGC_DS00142,BMG_DS000188,cutaneous fibrous histiocytoma
+BMGC_DS00143,BMG_DS000190,angioedema
+BMGC_DS00144,BMG_DS000191,Anhidrosis
+BMGC_DS00145,BMG_DS000193,aniridia
+BMGC_DS00146,BMG_DS000196,Anisometropia
+BMGC_DS00147,BMG_DS000197,autoimmune disease
+BMGC_DS00148,BMG_DS000198,ankylosis
+BMGC_DS00149,BMG_DS000201,nominal aphasia
+BMGC_DS00150,BMG_DS000202,Anorexia
+BMGC_DS00151,BMG_DS000203,anorexia nervosa
+BMGC_DS00152,BMG_DS000204,anosmia
+BMGC_DS00153,BMG_DS000205,Anovulation
+BMGC_DS00154,BMG_DS000206,Anterior Compartment Syndrome
+BMGC_DS00155,BMG_DS000207,Anthracosilicosis
+BMGC_DS00156,BMG_DS000208,Anthracosis
+BMGC_DS00157,BMG_DS000209,anthrax infection
+BMGC_DS00158,BMG_DS000210,Cutaneous anthrax
+BMGC_DS00159,BMG_DS000211,Antibody Deficiency Syndrome
+BMGC_DS00160,BMG_DS000212,antisocial personality disorder
+BMGC_DS00161,BMG_DS000213,Anuria
+BMGC_DS00162,BMG_DS000214,Anus Diseases
+BMGC_DS00163,BMG_DS000215,anus neoplasm
+BMGC_DS00164,BMG_DS000216,imperforate anus
+BMGC_DS00165,BMG_DS000217,anxiety
+BMGC_DS00166,BMG_DS000218,anxiety disorder
+BMGC_DS00167,BMG_DS000219,separation anxiety disorder
+BMGC_DS00168,BMG_DS000220,Aortic Aneurysm
+BMGC_DS00169,BMG_DS000221,Aortic Arch Syndromes
+BMGC_DS00170,BMG_DS000222,aorta coarctation
+BMGC_DS00171,BMG_DS000223,Aortic Diseases
+BMGC_DS00172,BMG_DS000224,Aortic Rupture
+BMGC_DS00173,BMG_DS000225,Supravalvular aortic stenosis
+BMGC_DS00174,BMG_DS000227,Aortic Valve Insufficiency
+BMGC_DS00175,BMG_DS000228,Aortic Valve Prolapse
+BMGC_DS00176,BMG_DS000229,aortic valve stenosis
+BMGC_DS00177,BMG_DS000230,Aortitis
+BMGC_DS00178,BMG_DS000231,Aortitis Syndrome
+BMGC_DS00179,BMG_DS000234,aphasia
+BMGC_DS00180,BMG_DS000235,appendiceal neoplasm
+BMGC_DS00181,BMG_DS000236,Appendicitis
+BMGC_DS00182,BMG_DS000237,apraxia
+BMGC_DS00183,BMG_DS000238,Arachnoiditis
+BMGC_DS00184,BMG_DS000240,Arbovirus Infections
+BMGC_DS00185,BMG_DS000241,Arcus Senilis
+BMGC_DS00186,BMG_DS000242,Arenaviridae Infections
+BMGC_DS00187,BMG_DS000243,Chiari malformation
+BMGC_DS00188,BMG_DS000245,Cardiac Arrhythmia
+BMGC_DS00189,BMG_DS000247,Arterial Occlusive Diseases
+BMGC_DS00190,BMG_DS000249,Arteriosclerosis
+BMGC_DS00191,BMG_DS000250,Arteriosclerosis Obliterans
+BMGC_DS00192,BMG_DS000251,arteritis
+BMGC_DS00193,BMG_DS000253,Arthritis
+BMGC_DS00194,BMG_DS000254,"Arthritis, Gouty"
+BMGC_DS00195,BMG_DS000255,"Arthritis, Infectious"
+BMGC_DS00196,BMG_DS000256,"Arthritis, Psoriatic"
+BMGC_DS00197,BMG_DS000257,Rheumatoid Arthritis
+BMGC_DS00198,BMG_DS000259,"Arthritis, Viral"
+BMGC_DS00199,BMG_DS000261,neurogenic arthropathy
+BMGC_DS00200,BMG_DS000262,Arthus Reaction
+BMGC_DS00201,BMG_DS000263,articulation disorder
+BMGC_DS00202,BMG_DS000264,Asbestosis
+BMGC_DS00203,BMG_DS000265,Ascariasis
+BMGC_DS00204,BMG_DS000266,Ascaridiasis
+BMGC_DS00205,BMG_DS000267,Ascites
+BMGC_DS00206,BMG_DS000268,Ascorbic Acid Deficiency
+BMGC_DS00207,BMG_DS000269,osteonecrosis
+BMGC_DS00208,BMG_DS000270,Aspergillosis
+BMGC_DS00209,BMG_DS000271,"Aspergillosis, Allergic Bronchopulmonary"
+BMGC_DS00210,BMG_DS000273,Asphyxia Neonatorum
+BMGC_DS00211,BMG_DS000277,Asthma
+BMGC_DS00212,BMG_DS000279,Astigmatism
+BMGC_DS00213,BMG_DS000280,astrocytoma (excluding glioblastoma)
+BMGC_DS00214,BMG_DS000281,Ataxia Telangiectasia
+BMGC_DS00215,BMG_DS000282,"Ataxias, Hereditary"
+BMGC_DS00216,BMG_DS000283,Atherosclerosis
+BMGC_DS00217,BMG_DS000285,Athetosis
+BMGC_DS00218,BMG_DS000288,Atrial Fibrillation
+BMGC_DS00219,BMG_DS000289,atrial flutter
+BMGC_DS00220,BMG_DS000290,Atrioventricular Block
+BMGC_DS00221,BMG_DS000293,atrioventricular dissociation
+BMGC_DS00222,BMG_DS000294,autism
+BMGC_DS00223,BMG_DS000295,Autoimmune Diseases
+BMGC_DS00224,BMG_DS000296,avoidant personality disorder
+BMGC_DS00225,BMG_DS000298,Azoospermia
+BMGC_DS00226,BMG_DS000299,Babesiosis
+BMGC_DS00227,BMG_DS000300,Nonproliferative diabetic retinopathy
+BMGC_DS00228,BMG_DS000301,exudative vitreoretinopathy
+BMGC_DS00229,BMG_DS000302,bacterial infectious disease with sepsis
+BMGC_DS00230,BMG_DS000305,Bacterial Infections
+BMGC_DS00231,BMG_DS000306,"Pneumonia, Bacterial"
+BMGC_DS00232,BMG_DS000307,bacteriuria
+BMGC_DS00233,BMG_DS000309,Bagassosis
+BMGC_DS00234,BMG_DS000310,Balanitis
+BMGC_DS00235,BMG_DS000311,Balanoposthitis
+BMGC_DS00236,BMG_DS000312,Balantidiasis
+BMGC_DS00237,BMG_DS000313,Balkan Nephropathy
+BMGC_DS00238,BMG_DS000314,Balo's Concentric Sclerosis
+BMGC_DS00239,BMG_DS000316,Barrett Esophagus
+BMGC_DS00240,BMG_DS000317,Cyst of Bartholin's gland duct
+BMGC_DS00241,BMG_DS000319,Bartonella Infections
+BMGC_DS00242,BMG_DS000321,Bartter Disease
+BMGC_DS00243,BMG_DS000322,nevoid basal cell carcinoma syndrome
+BMGC_DS00244,BMG_DS000323,Basal Ganglia Diseases
+BMGC_DS00245,BMG_DS000324,Basilar Artery Insufficiency
+BMGC_DS00246,BMG_DS000326,Beckwith-Wiedemann Syndrome
+BMGC_DS00247,BMG_DS000327,mental disorder
+BMGC_DS00248,BMG_DS000328,Behcet Syndrome
+BMGC_DS00249,BMG_DS000329,Bejel
+BMGC_DS00250,BMG_DS000330,benign colon neoplasm
+BMGC_DS00251,BMG_DS000334,Beriberi
+BMGC_DS00252,BMG_DS000335,Bernard-Soulier Syndrome
+BMGC_DS00253,BMG_DS000337,berylliosis
+BMGC_DS00254,BMG_DS000339,beta Thalassemia
+BMGC_DS00255,BMG_DS000340,Bile Duct Diseases
+BMGC_DS00256,BMG_DS000341,bile duct neoplasm
+BMGC_DS00257,BMG_DS000342,"Cholestasis, Extrahepatic"
+BMGC_DS00258,BMG_DS000343,Bile Reflux
+BMGC_DS00259,BMG_DS000344,biliary atresia
+BMGC_DS00260,BMG_DS000345,Biliary Dyskinesia
+BMGC_DS00261,BMG_DS000346,Biliary Tract Diseases
+BMGC_DS00262,BMG_DS000347,biliary tract neoplasm
+BMGC_DS00263,BMG_DS000349,Binocular vision disorder
+BMGC_DS00264,BMG_DS000350,bipolar disorder
+BMGC_DS00265,BMG_DS000351,bipolar depression
+BMGC_DS00266,BMG_DS000352,Bird Diseases
+BMGC_DS00267,BMG_DS000353,Bird Fancier's Lung
+BMGC_DS00268,BMG_DS000354,Blackwater Fever
+BMGC_DS00269,BMG_DS000355,Urinary bladder stone (disorder)
+BMGC_DS00270,BMG_DS000356,urinary bladder cancer
+BMGC_DS00271,BMG_DS000357,Urinary Bladder Diseases
+BMGC_DS00272,BMG_DS000358,Bladder Exstrophy
+BMGC_DS00273,BMG_DS000359,Bladder neck obstruction
+BMGC_DS00274,BMG_DS000360,urinary bladder neoplasm
+BMGC_DS00275,BMG_DS000361,Neurogenic Urinary Bladder
+BMGC_DS00276,BMG_DS000362,"blast phase chronic myelogenous leukemia, BCR-ABL1 positive"
+BMGC_DS00277,BMG_DS000363,Blastomycosis
+BMGC_DS00278,BMG_DS000364,Gilchrist Disease
+BMGC_DS00279,BMG_DS000369,Blepharitis
+BMGC_DS00280,BMG_DS000370,Blepharochalasis
+BMGC_DS00281,BMG_DS000371,Blepharoconjunctivitis
+BMGC_DS00282,BMG_DS000372,blepharophimosis
+BMGC_DS00283,BMG_DS000373,Blepharoptosis
+BMGC_DS00284,BMG_DS000374,Blepharospasm
+BMGC_DS00285,BMG_DS000375,Blind Loop Syndrome
+BMGC_DS00286,BMG_DS000376,Blood Coagulation Disorders
+BMGC_DS00287,BMG_DS000377,blood group incompatibility
+BMGC_DS00288,BMG_DS000378,Blood Platelet Disorders
+BMGC_DS00289,BMG_DS000379,Blood Protein Disorders
+BMGC_DS00290,BMG_DS000380,Bloom Syndrome
+BMGC_DS00291,BMG_DS000383,Bone Diseases
+BMGC_DS00292,BMG_DS000384,"Bone Diseases, Developmental"
+BMGC_DS00293,BMG_DS000385,"Bone Diseases, Endocrine"
+BMGC_DS00294,BMG_DS000387,metabolic bone disorder
+BMGC_DS00295,BMG_DS000388,Bone Marrow Diseases
+BMGC_DS00296,BMG_DS000389,bone cancer
+BMGC_DS00297,BMG_DS000390,bone resorption disease
+BMGC_DS00298,BMG_DS000392,borderline personality disorder
+BMGC_DS00299,BMG_DS000393,Bordetella Infections
+BMGC_DS00300,BMG_DS000394,Borna Disease
+BMGC_DS00301,BMG_DS000397,botulism
+BMGC_DS00302,BMG_DS000398,Boutonneuse Fever
+BMGC_DS00303,BMG_DS000400,Bowen disease of the skin
+BMGC_DS00304,BMG_DS000401,Brachial plexus lesion
+BMGC_DS00305,BMG_DS000402,Brain Abscess
+BMGC_DS00306,BMG_DS000403,"Brain Damage, Chronic"
+BMGC_DS00307,BMG_DS000404,Brain Diseases
+BMGC_DS00308,BMG_DS000405,"Brain Diseases, Metabolic"
+BMGC_DS00309,BMG_DS000406,brain edema
+BMGC_DS00310,BMG_DS000407,brain neoplasm
+BMGC_DS00311,BMG_DS000408,Branch Retinal Artery Occlusion
+BMGC_DS00312,BMG_DS000409,breast cancer
+BMGC_DS00313,BMG_DS000410,breast cyst
+BMGC_DS00314,BMG_DS000411,Breast Diseases
+BMGC_DS00315,BMG_DS000413,Brill-Zinsser Disease
+BMGC_DS00316,BMG_DS000415,Bronchial Diseases
+BMGC_DS00317,BMG_DS000416,bronchial neoplasm
+BMGC_DS00318,BMG_DS000417,Bronchospasm
+BMGC_DS00319,BMG_DS000418,Bronchiectasis
+BMGC_DS00320,BMG_DS000419,Bronchiolitis
+BMGC_DS00321,BMG_DS000420,Bronchiolitis Obliterans
+BMGC_DS00322,BMG_DS000421,"Bronchiolitis, Viral"
+BMGC_DS00323,BMG_DS000422,Bronchitis
+BMGC_DS00324,BMG_DS000424,Bronchopneumonia
+BMGC_DS00325,BMG_DS000425,Bronchopulmonary Dysplasia
+BMGC_DS00326,BMG_DS000426,Brucellosis
+BMGC_DS00327,BMG_DS000427,bruxism
+BMGC_DS00328,BMG_DS000428,bulimia nervosa
+BMGC_DS00329,BMG_DS000429,Bundle-Branch Block
+BMGC_DS00330,BMG_DS000430,Bunostomiasis
+BMGC_DS00331,BMG_DS000433,Burkitt lymphoma
+BMGC_DS00332,BMG_DS000435,Burning Mouth Syndrome
+BMGC_DS00333,BMG_DS000436,Bursitis
+BMGC_DS00334,BMG_DS000437,Byssinosis
+BMGC_DS00335,BMG_DS000438,calcinosis
+BMGC_DS00336,BMG_DS000440,Calciphylaxis
+BMGC_DS00337,BMG_DS000441,Calcium Metabolism Disorders
+BMGC_DS00338,BMG_DS000442,cholelithiasis
+BMGC_DS00339,BMG_DS000445,campylobacteriosis
+BMGC_DS00340,BMG_DS000446,cancer
+BMGC_DS00341,BMG_DS000447,Candidiasis
+BMGC_DS00342,BMG_DS000448,Candidiasis of skin and nails
+BMGC_DS00343,BMG_DS000449,"Candidiasis, Chronic Mucocutaneous"
+BMGC_DS00344,BMG_DS000450,cutaneous candidiasis
+BMGC_DS00345,BMG_DS000451,Mucocutaneous candidiasis
+BMGC_DS00346,BMG_DS000452,Oral candidiasis
+BMGC_DS00347,BMG_DS000453,Candidiasis of vagina
+BMGC_DS00348,BMG_DS000455,cannabis abuse
+BMGC_DS00349,BMG_DS000456,cannabis dependence
+BMGC_DS00350,BMG_DS000457,Capgras syndrome
+BMGC_DS00351,BMG_DS000458,Capillariasis
+BMGC_DS00352,BMG_DS000461,Caplan Syndrome
+BMGC_DS00353,BMG_DS000462,"Carbohydrate Metabolism, Inborn Errors"
+BMGC_DS00354,BMG_DS000464,carbuncle
+BMGC_DS00355,BMG_DS000467,carcinoma
+BMGC_DS00356,BMG_DS000468,in situ carcinoma
+BMGC_DS00357,BMG_DS000469,malignant colon neoplasm
+BMGC_DS00358,BMG_DS000470,endometrial cancer
+BMGC_DS00359,BMG_DS000471,female breast carcinoma
+BMGC_DS00360,BMG_DS000472,larynx cancer
+BMGC_DS00361,BMG_DS000473,prostate adenocarcinoma
+BMGC_DS00362,BMG_DS000474,rectal carcinoma
+BMGC_DS00363,BMG_DS000475,skin cancer
+BMGC_DS00364,BMG_DS000476,thyroid cancer
+BMGC_DS00365,BMG_DS000477,basal cell carcinoma
+BMGC_DS00366,BMG_DS000478,basosquamous carcinoma
+BMGC_DS00367,BMG_DS000479,minimally invasive lung adenocarcinoma
+BMGC_DS00368,BMG_DS000480,bronchogenic carcinoma
+BMGC_DS00369,BMG_DS000481,ductal breast carcinoma in situ
+BMGC_DS00370,BMG_DS000482,Ehrlich tumor carcinoma
+BMGC_DS00371,BMG_DS000484,cutaneous neuroendocrine carcinoma
+BMGC_DS00372,BMG_DS000485,mucinous adenocarcinoma
+BMGC_DS00373,BMG_DS000486,non-small cell lung carcinoma
+BMGC_DS00374,BMG_DS000487,papillary carcinoma
+BMGC_DS00375,BMG_DS000488,renal cell carcinoma
+BMGC_DS00376,BMG_DS000489,scirrhous adenocarcinoma
+BMGC_DS00377,BMG_DS000490,squamous cell carcinoma
+BMGC_DS00378,BMG_DS000491,transitional cell carcinoma
+BMGC_DS00379,BMG_DS000492,carcinosarcoma
+BMGC_DS00380,BMG_DS000493,Cardiac Tamponade
+BMGC_DS00381,BMG_DS000494,"Cardiomyopathy, Alcoholic"
+BMGC_DS00382,BMG_DS000495,"Cardiomyopathy, Dilated"
+BMGC_DS00383,BMG_DS000496,Hypertrophic Cardiomyopathy
+BMGC_DS00384,BMG_DS000497,Restrictive cardiomyopathy
+BMGC_DS00385,BMG_DS000498,Cardiovascular Diseases
+BMGC_DS00386,BMG_DS000499,Carotid Artery Diseases
+BMGC_DS00387,BMG_DS000500,Carotid Artery Thrombosis
+BMGC_DS00388,BMG_DS000502,Carotid Stenosis
+BMGC_DS00389,BMG_DS000504,Carpal Tunnel Syndrome
+BMGC_DS00390,BMG_DS000505,Carsickness
+BMGC_DS00391,BMG_DS000506,Cartilage Diseases
+BMGC_DS00392,BMG_DS000507,Cat Diseases
+BMGC_DS00393,BMG_DS000508,Cat-Scratch Disease
+BMGC_DS00394,BMG_DS000509,Cataplexy
+BMGC_DS00395,BMG_DS000511,catatonia
+BMGC_DS00396,BMG_DS000512,Cattle Diseases
+BMGC_DS00397,BMG_DS000514,Causalgia
+BMGC_DS00398,BMG_DS000515,Cecal Diseases
+BMGC_DS00399,BMG_DS000516,cecal neoplasm
+BMGC_DS00400,BMG_DS000517,Celiac Disease
+BMGC_DS00401,BMG_DS000518,Cellulitis
+BMGC_DS00402,BMG_DS000519,tinea unguium
+BMGC_DS00403,BMG_DS000521,Cellulitis of hand
+BMGC_DS00404,BMG_DS000523,CNS disorder
+BMGC_DS00405,BMG_DS000524,Central Nervous System Infection
+BMGC_DS00406,BMG_DS000525,Central Retinal Artery Occlusion
+BMGC_DS00407,BMG_DS000528,Cerebellar Ataxia
+BMGC_DS00408,BMG_DS000529,Cerebellar Diseases
+BMGC_DS00409,BMG_DS000530,Myoclonic Cerebellar Dyssynergia
+BMGC_DS00410,BMG_DS000531,cerebellar neoplasm
+BMGC_DS00411,BMG_DS000532,Intracranial Aneurysm
+BMGC_DS00412,BMG_DS000533,Intracranial Arteriosclerosis
+BMGC_DS00413,BMG_DS000534,arteriovenous malformations of the brain
+BMGC_DS00414,BMG_DS000535,Cerebral arteritis
+BMGC_DS00415,BMG_DS000536,Cerebral Arterial Diseases
+BMGC_DS00416,BMG_DS000537,Cerebral Atherosclerosis
+BMGC_DS00417,BMG_DS000538,Cerebral Embolism
+BMGC_DS00418,BMG_DS000539,Intracranial Embolism and Thrombosis
+BMGC_DS00419,BMG_DS000540,Cerebral Infarction
+BMGC_DS00420,BMG_DS000541,Brain Ischemia
+BMGC_DS00421,BMG_DS000542,Transient Ischemic Attack
+BMGC_DS00422,BMG_DS000543,Cerebral lipidosis
+BMGC_DS00423,BMG_DS000544,Cerebral Palsy
+BMGC_DS00424,BMG_DS000545,Diffuse Cerebral Sclerosis of Schilder
+BMGC_DS00425,BMG_DS000546,cerebral ventricle cancer
+BMGC_DS00426,BMG_DS000547,Cerebrospinal meningitis
+BMGC_DS00427,BMG_DS000550,Cerebrovascular Disorders
+BMGC_DS00428,BMG_DS000551,Certain types of iridocyclitis
+BMGC_DS00429,BMG_DS000552,cervical cancer
+BMGC_DS00430,BMG_DS000553,Cervical Migraine Syndrome
+BMGC_DS00431,BMG_DS000556,Uterine Cervicitis
+BMGC_DS00432,BMG_DS000557,cervicitis
+BMGC_DS00433,BMG_DS000558,Cervico-Brachial Neuralgia
+BMGC_DS00434,BMG_DS000560,Cervix Diseases
+BMGC_DS00435,BMG_DS000562,Cervix Erosion
+BMGC_DS00436,BMG_DS000564,cervical incompetence
+BMGC_DS00437,BMG_DS000565,uterine cervix neoplasm
+BMGC_DS00438,BMG_DS000569,Meibomian Cyst
+BMGC_DS00439,BMG_DS000570,syphilis
+BMGC_DS00440,BMG_DS000572,Chancroid
+BMGC_DS00441,BMG_DS000573,Charcot-Marie-Tooth Disease
+BMGC_DS00442,BMG_DS000574,Chediak-Higashi Syndrome
+BMGC_DS00443,BMG_DS000576,Cheilitis
+BMGC_DS00444,BMG_DS000577,Cherubism
+BMGC_DS00445,BMG_DS000578,Chiari-Frommel Syndrome
+BMGC_DS00446,BMG_DS000579,Chickenpox
+BMGC_DS00447,BMG_DS000580,Chikungunya Fever
+BMGC_DS00448,BMG_DS000581,Child Nutrition Disorders
+BMGC_DS00449,BMG_DS000582,Glutamate Monosodium Sensitivity
+BMGC_DS00450,BMG_DS000583,Chlamydia Infections
+BMGC_DS00451,BMG_DS000585,Asiderotic anemia
+BMGC_DS00452,BMG_DS000586,choanal atresia
+BMGC_DS00453,BMG_DS000588,bile duct adenoma
+BMGC_DS00454,BMG_DS000589,Cholangitis
+BMGC_DS00455,BMG_DS000590,Primary Biliary Cholangitis
+BMGC_DS00456,BMG_DS000591,"Cholangitis, Sclerosing"
+BMGC_DS00457,BMG_DS000592,Cholecystitis
+BMGC_DS00458,BMG_DS000593,bile duct cyst
+BMGC_DS00459,BMG_DS000594,Cholelithiasis
+BMGC_DS00460,BMG_DS000595,Cholera
+BMGC_DS00461,BMG_DS000596,Cholestasis
+BMGC_DS00462,BMG_DS000597,Intrahepatic Cholestasis
+BMGC_DS00463,BMG_DS000598,Cholesteatoma
+BMGC_DS00464,BMG_DS000599,Cholesteatoma of middle ear and mastoid
+BMGC_DS00465,BMG_DS000600,Cholesterol Ester Storage Disease
+BMGC_DS00466,BMG_DS000601,Choline Deficiency
+BMGC_DS00467,BMG_DS000602,chondroblastoma
+BMGC_DS00468,BMG_DS000603,Chondrodysplasia Punctata
+BMGC_DS00469,BMG_DS000604,Congenital anomaly of cartilage
+BMGC_DS00470,BMG_DS000605,Chondromalacia Patellae
+BMGC_DS00471,BMG_DS000607,chondrosarcoma
+BMGC_DS00472,BMG_DS000608,chordoma
+BMGC_DS00473,BMG_DS000609,Chorea
+BMGC_DS00474,BMG_DS000611,Chorioamnionitis
+BMGC_DS00475,BMG_DS000612,choriocarcinoma
+BMGC_DS00476,BMG_DS000613,chorioretinal scar
+BMGC_DS00477,BMG_DS000614,Chorioretinitis
+BMGC_DS00478,BMG_DS000615,Choroid Diseases
+BMGC_DS00479,BMG_DS000616,choroid neoplasm
+BMGC_DS00480,BMG_DS000617,Choroideremia
+BMGC_DS00481,BMG_DS000618,Choroiditis
+BMGC_DS00482,BMG_DS000619,Hemophilia B
+BMGC_DS00483,BMG_DS000620,Chromoblastomycosis
+BMGC_DS00484,BMG_DS000622,Congenital chromosomal disease
+BMGC_DS00485,BMG_DS000623,"Bronchitis, Chronic"
+BMGC_DS00486,BMG_DS000625,Cryptogenic pulmonary eosinophilia
+BMGC_DS00487,BMG_DS000626,Chronic ethmoidal sinusitis
+BMGC_DS00488,BMG_DS000627,Chronic frontal sinusitis
+BMGC_DS00489,BMG_DS000628,Chronic gingivitis
+BMGC_DS00490,BMG_DS000630,Chronic maxillary sinusitis
+BMGC_DS00491,BMG_DS000631,chronic tic disorder
+BMGC_DS00492,BMG_DS000632,Chronic osteomyelitis
+BMGC_DS00493,BMG_DS000633,Chronic rhinitis
+BMGC_DS00494,BMG_DS000634,Chronic sphenoidal sinusitis
+BMGC_DS00495,BMG_DS000635,Chronically Ill
+BMGC_DS00496,BMG_DS000636,Eosinophilic granulomatosis with polyangiitis
+BMGC_DS00497,BMG_DS000637,Chylous Ascites
+BMGC_DS00498,BMG_DS000638,Chylothorax
+BMGC_DS00499,BMG_DS000639,Ciliary Motility Disorders
+BMGC_DS00500,BMG_DS000640,Cirrhosis of liver without mention of alcohol
+BMGC_DS00501,BMG_DS000641,isolated cleft lip
+BMGC_DS00502,BMG_DS000642,cleft palate
+BMGC_DS00503,BMG_DS000643,Cleidocranial Dysplasia
+BMGC_DS00504,BMG_DS000644,Clonorchiasis
+BMGC_DS00505,BMG_DS000646,clubfoot
+BMGC_DS00506,BMG_DS000647,Cluster Headache
+BMGC_DS00507,BMG_DS000648,cocaine abuse
+BMGC_DS00508,BMG_DS000649,Coccidioidomycosis
+BMGC_DS00509,BMG_DS000650,Coccidiosis
+BMGC_DS00510,BMG_DS000652,Cochlear Diseases
+BMGC_DS00511,BMG_DS000653,Cockayne Syndrome
+BMGC_DS00512,BMG_DS000657,Coin lesion of lung
+BMGC_DS00513,BMG_DS000658,Cold Panniculitis
+BMGC_DS00514,BMG_DS000659,Colitis
+BMGC_DS00515,BMG_DS000660,Ulcerative Colitis
+BMGC_DS00516,BMG_DS000661,Collagen Diseases
+BMGC_DS00517,BMG_DS000662,coloboma
+BMGC_DS00518,BMG_DS000663,Colonic Diseases
+BMGC_DS00519,BMG_DS000664,"Colonic Diseases, Functional"
+BMGC_DS00520,BMG_DS000665,colonic neoplasm
+BMGC_DS00521,BMG_DS000666,polyp of colon
+BMGC_DS00522,BMG_DS000667,Colonic Pseudo-Obstruction
+BMGC_DS00523,BMG_DS000668,Colorado Tick Fever
+BMGC_DS00524,BMG_DS000669,colorectal carcinoma
+BMGC_DS00525,BMG_DS000670,colorectal neoplasm
+BMGC_DS00526,BMG_DS000671,Lynch syndrome
+BMGC_DS00527,BMG_DS000672,Comatose
+BMGC_DS00528,BMG_DS000673,combat disorder
+BMGC_DS00529,BMG_DS000674,Common Bile Duct Diseases
+BMGC_DS00530,BMG_DS000675,common bile duct neoplasm
+BMGC_DS00531,BMG_DS000676,Common Cold
+BMGC_DS00532,BMG_DS000677,Common Variable Immunodeficiency
+BMGC_DS00533,BMG_DS000678,Communicable Diseases
+BMGC_DS00534,BMG_DS000679,Communicating Hydrocephalus
+BMGC_DS00535,BMG_DS000680,communication disorder
+BMGC_DS00536,BMG_DS000681,compartment syndrome
+BMGC_DS00537,BMG_DS000682,Compression of brain
+BMGC_DS00538,BMG_DS000683,obsessive-compulsive personality disorder
+BMGC_DS00539,BMG_DS000684,Condylomata Acuminata
+BMGC_DS00540,BMG_DS000685,congenital macroglossia
+BMGC_DS00541,BMG_DS000688,"Hepatic Fibrosis, Congenital"
+BMGC_DS00542,BMG_DS000689,Conjunctival Diseases
+BMGC_DS00543,BMG_DS000690,conjunctival tumor
+BMGC_DS00544,BMG_DS000691,Conjunctivitis
+BMGC_DS00545,BMG_DS000692,"Conjunctivitis, Acute Hemorrhagic"
+BMGC_DS00546,BMG_DS000693,Allergic Conjunctivitis
+BMGC_DS00547,BMG_DS000694,Bacterial conjunctivitis
+BMGC_DS00548,BMG_DS000695,"Conjunctivitis, Giant Papillary"
+BMGC_DS00549,BMG_DS000696,Inclusion conjunctivitis
+BMGC_DS00550,BMG_DS000697,"Conjunctivitis, Vernal"
+BMGC_DS00551,BMG_DS000699,Connective Tissue Diseases
+BMGC_DS00552,BMG_DS000700,constipation disorder
+BMGC_DS00553,BMG_DS000701,conversion disorder
+BMGC_DS00554,BMG_DS000702,Febrile Convulsions
+BMGC_DS00555,BMG_DS000704,Corneal Diseases
+BMGC_DS00556,BMG_DS000705,Hereditary corneal dystrophy
+BMGC_DS00557,BMG_DS000706,Corneal dystrophy
+BMGC_DS00558,BMG_DS000707,corneal edema
+BMGC_DS00559,BMG_DS000708,Corneal Ulcer
+BMGC_DS00560,BMG_DS000709,Coronary Aneurysm
+BMGC_DS00561,BMG_DS000710,Coronary Arteriosclerosis
+BMGC_DS00562,BMG_DS000711,Coronary heart disease
+BMGC_DS00563,BMG_DS000712,Coronary Thrombosis
+BMGC_DS00564,BMG_DS000713,Coronary Artery Vasospasm
+BMGC_DS00565,BMG_DS000715,Corpus Luteum Cyst
+BMGC_DS00566,BMG_DS000718,Cowpox
+BMGC_DS00567,BMG_DS000719,Coxsackievirus Infections
+BMGC_DS00568,BMG_DS000721,cranial nerve neuropathy
+BMGC_DS00569,BMG_DS000722,cranial nerve neoplasm
+BMGC_DS00570,BMG_DS000724,Craniofacial Dysostosis
+BMGC_DS00571,BMG_DS000725,craniopharyngioma
+BMGC_DS00572,BMG_DS000726,Craniosynostosis
+BMGC_DS00573,BMG_DS000727,Congenital Hypothyroidism
+BMGC_DS00574,BMG_DS000728,Cri-du-Chat Syndrome
+BMGC_DS00575,BMG_DS000729,Crigler-Najjar syndrome type 1
+BMGC_DS00576,BMG_DS000731,Critical Illness
+BMGC_DS00577,BMG_DS000732,Crohn Disease
+BMGC_DS00578,BMG_DS000734,Croup
+BMGC_DS00579,BMG_DS000736,Cruveilhier-Baumgarten Syndrome
+BMGC_DS00580,BMG_DS000737,Cryoglobulinemia
+BMGC_DS00581,BMG_DS000738,Infection by Cryptococcus neoformans
+BMGC_DS00582,BMG_DS000739,cryptorchidism
+BMGC_DS00583,BMG_DS000740,Cryptosporidiosis
+BMGC_DS00584,BMG_DS000741,Curling Ulcer
+BMGC_DS00585,BMG_DS000742,Cushing Syndrome
+BMGC_DS00586,BMG_DS000744,Cutis Laxa
+BMGC_DS00587,BMG_DS000745,Cyclitis
+BMGC_DS00588,BMG_DS000746,cyclothymic disorder
+BMGC_DS00589,BMG_DS000747,adenoid cystic carcinoma
+BMGC_DS00590,BMG_DS000748,cystadenocarcinoma
+BMGC_DS00591,BMG_DS000749,cystadenoma
+BMGC_DS00592,BMG_DS000754,Cystic Fibrosis
+BMGC_DS00593,BMG_DS000755,Cysticercosis
+BMGC_DS00594,BMG_DS000756,Cystinuria
+BMGC_DS00595,BMG_DS000757,Cystitis
+BMGC_DS00596,BMG_DS000759,phyllodes tumor
+BMGC_DS00597,BMG_DS000760,Cytomegalovirus Infections
+BMGC_DS00598,BMG_DS000761,Dacryocystitis
+BMGC_DS00599,BMG_DS000762,Dandy-Walker Syndrome
+BMGC_DS00600,BMG_DS000763,Prelingual Deafness
+BMGC_DS00601,BMG_DS000767,Deficiency Diseases
+BMGC_DS00602,BMG_DS000770,Deglutition Disorders
+BMGC_DS00603,BMG_DS000771,Dehydration
+BMGC_DS00604,BMG_DS000772,Dejerine-Sottas Disease
+BMGC_DS00605,BMG_DS000773,delirium
+BMGC_DS00606,BMG_DS000774,hepatitis D virus infection
+BMGC_DS00607,BMG_DS000775,delusional disorder
+BMGC_DS00608,BMG_DS000776,Multi-infarct dementia
+BMGC_DS00609,BMG_DS000777,"Dementia, Vascular"
+BMGC_DS00610,BMG_DS000779,Demyelinating Diseases
+BMGC_DS00611,BMG_DS000780,Dengue Fever
+BMGC_DS00612,BMG_DS000781,Dental caries
+BMGC_DS00613,BMG_DS000783,Dental Enamel Hypoplasia
+BMGC_DS00614,BMG_DS000784,Dental Plaque
+BMGC_DS00615,BMG_DS000786,Dental Pulp Calcification
+BMGC_DS00616,BMG_DS000787,Dental Pulp Diseases
+BMGC_DS00617,BMG_DS000789,Dental Pulp Necrosis
+BMGC_DS00618,BMG_DS000791,Dentin Dysplasia
+BMGC_DS00619,BMG_DS000792,Dentin Sensitivity
+BMGC_DS00620,BMG_DS000794,dentinogenesis imperfecta
+BMGC_DS00621,BMG_DS000795,dependent personality disorder
+BMGC_DS00622,BMG_DS000796,depressive disorder
+BMGC_DS00623,BMG_DS000797,endogenous depression
+BMGC_DS00624,BMG_DS000798,neurotic disorder
+BMGC_DS00625,BMG_DS000799,depressive disorder
+BMGC_DS00626,BMG_DS000800,Dermatitis
+BMGC_DS00627,BMG_DS000801,Exfoliative dermatitis
+BMGC_DS00628,BMG_DS000802,Dermatitis Herpetiformis
+BMGC_DS00629,BMG_DS000803,"Dermatitis, Atopic"
+BMGC_DS00630,BMG_DS000804,Contact Dermatitis
+BMGC_DS00631,BMG_DS000806,Dermatomycoses
+BMGC_DS00632,BMG_DS000807,Dermatomyositis
+BMGC_DS00633,BMG_DS000808,Dermatophytosis
+BMGC_DS00634,BMG_DS000809,Dermatophytosis of groin and perianal area
+BMGC_DS00635,BMG_DS000810,dermatophytosis of scalp or beard
+BMGC_DS00636,BMG_DS000811,Scleroderma
+BMGC_DS00637,BMG_DS000812,Dermatosis Papulosa Nigra
+BMGC_DS00638,BMG_DS000813,dermoid cyst
+BMGC_DS00639,BMG_DS000814,developmental coordination disorder
+BMGC_DS00640,BMG_DS000815,dextrocardia
+BMGC_DS00641,BMG_DS000816,Diabetes
+BMGC_DS00642,BMG_DS000817,Diabetes Insipidus
+BMGC_DS00643,BMG_DS000818,Diabetes Mellitus
+BMGC_DS00644,BMG_DS000819,"Diabetes Mellitus, Insulin-Dependent"
+BMGC_DS00645,BMG_DS000820,Lipoatrophic Diabetes Mellitus
+BMGC_DS00646,BMG_DS000821,"Diabetes Mellitus, Non-Insulin-Dependent"
+BMGC_DS00647,BMG_DS000823,Diabetic peripheral angiopathy
+BMGC_DS00648,BMG_DS000824,Diabetic Angiopathies
+BMGC_DS00649,BMG_DS000825,Cataract due to diabetes mellitus
+BMGC_DS00650,BMG_DS000827,Diabetic Ketoacidosis
+BMGC_DS00651,BMG_DS000828,Diabetic Nephropathy
+BMGC_DS00652,BMG_DS000829,Diabetic Neuropathies
+BMGC_DS00653,BMG_DS000830,Diabetic Retinopathy
+BMGC_DS00654,BMG_DS000831,Diaper Rash
+BMGC_DS00655,BMG_DS000832,diaphragmatic eventration
+BMGC_DS00656,BMG_DS000834,Camurati-Engelmann Syndrome
+BMGC_DS00657,BMG_DS000836,VIPoma
+BMGC_DS00658,BMG_DS000837,diastematomyelia
+BMGC_DS00659,BMG_DS000838,Dicrocoeliasis
+BMGC_DS00660,BMG_DS000840,Dientamoebiasis
+BMGC_DS00661,BMG_DS000841,DiGeorge Syndrome
+BMGC_DS00662,BMG_DS000842,Digestive System Disorders
+BMGC_DS00663,BMG_DS000843,digestive system neoplasm
+BMGC_DS00664,BMG_DS000845,Dipetalonema Infections
+BMGC_DS00665,BMG_DS000846,Diphtheria
+BMGC_DS00666,BMG_DS000849,Cutaneous diphtheria
+BMGC_DS00667,BMG_DS000853,Diphyllobothriasis
+BMGC_DS00668,BMG_DS000854,Diplopia
+BMGC_DS00669,BMG_DS000855,Dirofilariasis
+BMGC_DS00670,BMG_DS000856,Discitis
+BMGC_DS00671,BMG_DS000857,Discrete Subaortic Stenosis
+BMGC_DS00672,BMG_DS000858,Disease
+BMGC_DS00673,BMG_DS000863,Iron Metabolism Disorders
+BMGC_DS00674,BMG_DS000864,Disorder of magnesium metabolism
+BMGC_DS00675,BMG_DS000865,disruptive behavior disorder
+BMGC_DS00676,BMG_DS000866,Dissecting aortic aneurysm
+BMGC_DS00677,BMG_DS000868,Disseminated Intravascular Coagulation
+BMGC_DS00678,BMG_DS000869,dissociative disorder
+BMGC_DS00679,BMG_DS000872,Diverticulitis
+BMGC_DS00680,BMG_DS000873,Colonic Diverticulitis
+BMGC_DS00681,BMG_DS000875,Diverticular disease of colon
+BMGC_DS00682,BMG_DS000877,Dog Diseases
+BMGC_DS00683,BMG_DS000878,double outlet right ventricle
+BMGC_DS00684,BMG_DS000880,Down Syndrome
+BMGC_DS00685,BMG_DS000881,Dracunculiasis
+BMGC_DS00686,BMG_DS000882,substance abuse
+BMGC_DS00687,BMG_DS000883,drug allergy
+BMGC_DS00688,BMG_DS000884,Dry Eye Syndromes
+BMGC_DS00689,BMG_DS000885,Alveolar periostitis
+BMGC_DS00690,BMG_DS000886,Duane Retraction Syndrome
+BMGC_DS00691,BMG_DS000887,"Muscular Dystrophy, Duchenne"
+BMGC_DS00692,BMG_DS000888,patent ductus arteriosus
+BMGC_DS00693,BMG_DS000889,Dumping Syndrome
+BMGC_DS00694,BMG_DS000890,Duodenal Diseases
+BMGC_DS00695,BMG_DS000891,tumor of duodenum
+BMGC_DS00696,BMG_DS000892,Duodenal Obstruction
+BMGC_DS00697,BMG_DS000893,Duodenal Ulcer
+BMGC_DS00698,BMG_DS000894,Duodenitis
+BMGC_DS00699,BMG_DS000895,Duodenogastric Reflux
+BMGC_DS00700,BMG_DS000896,Dupuytren Contracture
+BMGC_DS00701,BMG_DS000897,Dwarfism
+BMGC_DS00702,BMG_DS000898,Pituitary dwarfism
+BMGC_DS00703,BMG_DS000899,Dysautonomia
+BMGC_DS00704,BMG_DS000900,"Dysautonomia, Familial"
+BMGC_DS00705,BMG_DS000901,Dysentery
+BMGC_DS00706,BMG_DS000902,Amebic colitis
+BMGC_DS00707,BMG_DS000903,Shigella Infections
+BMGC_DS00708,BMG_DS000904,Dysgammaglobulinemia
+BMGC_DS00709,BMG_DS000905,dysgerminoma
+BMGC_DS00710,BMG_DS000906,"Dyskinesia, Drug-Induced"
+BMGC_DS00711,BMG_DS000907,alexia
+BMGC_DS00712,BMG_DS000908,Dysmenorrhea
+BMGC_DS00713,BMG_DS000909,Dysostoses
+BMGC_DS00714,BMG_DS000911,dyspepsia
+BMGC_DS00715,BMG_DS000912,functional gastric disease
+BMGC_DS00716,BMG_DS000914,dysthymic disorder
+BMGC_DS00717,BMG_DS000916,dystonic disorder
+BMGC_DS00718,BMG_DS000917,Dystonia Musculorum Deformans
+BMGC_DS00719,BMG_DS000918,Dystrophy of vulva
+BMGC_DS00720,BMG_DS000919,Ear Diseases
+BMGC_DS00721,BMG_DS000920,ear neoplasm
+BMGC_DS00722,BMG_DS000922,eating disorder
+BMGC_DS00723,BMG_DS000923,Ebstein anomaly
+BMGC_DS00724,BMG_DS000924,Echinococcosis
+BMGC_DS00725,BMG_DS000927,Echinostomiasis
+BMGC_DS00726,BMG_DS000928,echolalia
+BMGC_DS00727,BMG_DS000930,Eclampsia
+BMGC_DS00728,BMG_DS000931,Ecthyma
+BMGC_DS00729,BMG_DS000932,"Ecthyma, Contagious"
+BMGC_DS00730,BMG_DS000933,Ectodermal Dysplasia
+BMGC_DS00731,BMG_DS000934,Ectoparasitic Infestations
+BMGC_DS00732,BMG_DS000936,isolated ectopia lentis
+BMGC_DS00733,BMG_DS000937,"Ectromelia, Infectious"
+BMGC_DS00734,BMG_DS000938,Ectropion
+BMGC_DS00735,BMG_DS000939,Eczema
+BMGC_DS00736,BMG_DS000944,Ehlers-Danlos Syndrome
+BMGC_DS00737,BMG_DS000946,Elaeophoriasis
+BMGC_DS00738,BMG_DS000947,Elephantiasis
+BMGC_DS00739,BMG_DS000948,Filarial Elephantiases
+BMGC_DS00740,BMG_DS000949,"Elliptocytosis, Hereditary"
+BMGC_DS00741,BMG_DS000950,Ellis-Van Creveld Syndrome
+BMGC_DS00742,BMG_DS000953,Embryopathies
+BMGC_DS00743,BMG_DS000954,Empty Sella Syndrome
+BMGC_DS00744,BMG_DS000956,"Empyema, Gallbladder"
+BMGC_DS00745,BMG_DS000957,"Empyema, Pleural"
+BMGC_DS00746,BMG_DS000958,"Empyema, Tuberculous"
+BMGC_DS00747,BMG_DS000959,Encephalitis
+BMGC_DS00748,BMG_DS000960,encephalitis lethargica
+BMGC_DS00749,BMG_DS000961,"Encephalitis, California"
+BMGC_DS00750,BMG_DS000962,"Encephalitis, Central European"
+BMGC_DS00751,BMG_DS000963,Arbovirus encephalitis
+BMGC_DS00752,BMG_DS000964,Japanese Encephalitis
+BMGC_DS00753,BMG_DS000966,"Encephalomyelitis, Acute Disseminated"
+BMGC_DS00754,BMG_DS000967,"Encephalitis, St. Louis"
+BMGC_DS00755,BMG_DS000969,cephalocele
+BMGC_DS00756,BMG_DS000971,occipital encephalocele
+BMGC_DS00757,BMG_DS000972,Encephalomalacia
+BMGC_DS00758,BMG_DS000973,Encephalomyelitis
+BMGC_DS00759,BMG_DS000976,"Leukoencephalitis, Acute Hemorrhagic"
+BMGC_DS00760,BMG_DS000977,Venezuelan equine encephalomyelitis
+BMGC_DS00761,BMG_DS000978,Enchondromatosis
+BMGC_DS00762,BMG_DS000979,Endarteritis
+BMGC_DS00763,BMG_DS000980,atrioventricular septal defect
+BMGC_DS00764,BMG_DS000981,Endocardial Fibroelastosis
+BMGC_DS00765,BMG_DS000982,Endocarditis
+BMGC_DS00766,BMG_DS000983,Bacterial Endocarditis
+BMGC_DS00767,BMG_DS000985,Endocervicitis
+BMGC_DS00768,BMG_DS000986,Endocrine System Diseases
+BMGC_DS00769,BMG_DS000987,endocrine gland neoplasm
+BMGC_DS00770,BMG_DS000988,yolk sac tumor
+BMGC_DS00771,BMG_DS000989,endometrium neoplasm
+BMGC_DS00772,BMG_DS000990,Endometrial Hyperplasia
+BMGC_DS00773,BMG_DS000991,Endometriosis
+BMGC_DS00774,BMG_DS000992,Endometriosis of fallopian tube
+BMGC_DS00775,BMG_DS000993,Endometritis
+BMGC_DS00776,BMG_DS000996,Endophthalmitis
+BMGC_DS00777,BMG_DS000997,Parasitic endophthalmitis
+BMGC_DS00778,BMG_DS000998,Enophthalmos
+BMGC_DS00779,BMG_DS000999,Entamoebiasis
+BMGC_DS00780,BMG_DS001001,Enteritis
+BMGC_DS00781,BMG_DS001004,Enterobacteriaceae Infections
+BMGC_DS00782,BMG_DS001005,Enterocolitis
+BMGC_DS00783,BMG_DS001006,"Enterocolitis, Pseudomembranous"
+BMGC_DS00784,BMG_DS001009,Enterovirus Infections
+BMGC_DS00785,BMG_DS001010,Entropion
+BMGC_DS00786,BMG_DS001011,Enuresis
+BMGC_DS00787,BMG_DS001013,Eosinophilia
+BMGC_DS00788,BMG_DS001014,"Eosinophilia, Tropical"
+BMGC_DS00789,BMG_DS001017,ependymoma
+BMGC_DS00790,BMG_DS001018,Eperythrozoonosis
+BMGC_DS00791,BMG_DS001020,Epicondylitis
+BMGC_DS00792,BMG_DS001021,Epidemic keratoconjunctivitis
+BMGC_DS00793,BMG_DS001024,Toxic Epidermal Necrolysis
+BMGC_DS00794,BMG_DS001026,epidermodysplasia verruciformis
+BMGC_DS00795,BMG_DS001027,epidermolysis bullosa
+BMGC_DS00796,BMG_DS001028,Epidermophytosis
+BMGC_DS00797,BMG_DS001029,Epididymitis
+BMGC_DS00798,BMG_DS001030,epidural spinal canal neoplasm
+BMGC_DS00799,BMG_DS001031,Epiglottitis
+BMGC_DS00800,BMG_DS001032,Epilepsy
+BMGC_DS00801,BMG_DS001033,"Epilepsies, Partial"
+BMGC_DS00802,BMG_DS001034,"Epilepsy, Generalized"
+BMGC_DS00803,BMG_DS001035,Tonic-Clonic Epilepsy
+BMGC_DS00804,BMG_DS001036,Myoclonic Epilepsy
+BMGC_DS00805,BMG_DS001037,Absence Epilepsy
+BMGC_DS00806,BMG_DS001038,"Epilepsy, Temporal Lobe"
+BMGC_DS00807,BMG_DS001040,Uncinate Epilepsy
+BMGC_DS00808,BMG_DS001049,Erysipelas
+BMGC_DS00809,BMG_DS001053,Erythema Multiforme
+BMGC_DS00810,BMG_DS001054,Erythema Nodosum
+BMGC_DS00811,BMG_DS001056,Erythematosquamous dermatosis
+BMGC_DS00812,BMG_DS001057,Erythrasma
+BMGC_DS00813,BMG_DS001058,"Erythroblastosis, Fetal"
+BMGC_DS00814,BMG_DS001059,"Erythroderma, Maculopapular"
+BMGC_DS00815,BMG_DS001061,Erythromelalgia
+BMGC_DS00816,BMG_DS001062,Primary Erythermalgia
+BMGC_DS00817,BMG_DS001065,Escherichia coli Infections
+BMGC_DS00818,BMG_DS001066,Esophageal Achalasia
+BMGC_DS00819,BMG_DS001067,esophageal atresia
+BMGC_DS00820,BMG_DS001068,Esophageal Diseases
+BMGC_DS00821,BMG_DS001069,dyskinesia of esophagus
+BMGC_DS00822,BMG_DS001070,neoplasm of esophagus
+BMGC_DS00823,BMG_DS001072,Esophageal Stenosis
+BMGC_DS00824,BMG_DS001073,Esophageal Varices
+BMGC_DS00825,BMG_DS001074,Esophagitis
+BMGC_DS00826,BMG_DS001075,Peptic Esophagitis
+BMGC_DS00827,BMG_DS001076,Esotropia
+BMGC_DS00828,BMG_DS001078,Ethmoid Sinusitis
+BMGC_DS00829,BMG_DS001079,Euthyroid Sick Syndromes
+BMGC_DS00830,BMG_DS001080,exanthem
+BMGC_DS00831,BMG_DS001081,Exanthema Subitum
+BMGC_DS00832,BMG_DS001084,Exophthalmos
+BMGC_DS00833,BMG_DS001086,hereditary multiple osteochondromas
+BMGC_DS00834,BMG_DS001087,Exotropia
+BMGC_DS00835,BMG_DS001089,Extrapyramidal Disorders
+BMGC_DS00836,BMG_DS001090,Disorder of eye
+BMGC_DS00837,BMG_DS001091,"Eye Diseases, Hereditary"
+BMGC_DS00838,BMG_DS001092,Eye Infection
+BMGC_DS00839,BMG_DS001093,"Eye Infections, Bacterial"
+BMGC_DS00840,BMG_DS001094,fungal infection of eye
+BMGC_DS00841,BMG_DS001096,"Eye Infections, Viral"
+BMGC_DS00842,BMG_DS001097,eye neoplasm
+BMGC_DS00843,BMG_DS001098,Eyelid Diseases
+BMGC_DS00844,BMG_DS001099,eyelid neoplasm
+BMGC_DS00845,BMG_DS001100,Facial Dermatoses
+BMGC_DS00846,BMG_DS001101,Facial Hemiatrophy
+BMGC_DS00847,BMG_DS001102,Facial Nerve Diseases
+BMGC_DS00848,BMG_DS001103,Facial Neuralgia
+BMGC_DS00849,BMG_DS001104,Facial paralysis
+BMGC_DS00850,BMG_DS001106,factitious disorder
+BMGC_DS00851,BMG_DS001107,congenital factor V deficiency
+BMGC_DS00852,BMG_DS001108,Factor VII Deficiency
+BMGC_DS00853,BMG_DS001109,Factor X Deficiency
+BMGC_DS00854,BMG_DS001110,congenital factor XI deficiency
+BMGC_DS00855,BMG_DS001111,Factor XII Deficiency
+BMGC_DS00856,BMG_DS001112,congenital factor XIII deficiency
+BMGC_DS00857,BMG_DS001113,Failure to Thrive
+BMGC_DS00858,BMG_DS001114,Fallopian Tube Diseases
+BMGC_DS00859,BMG_DS001115,fallopian tube neoplasm
+BMGC_DS00860,BMG_DS001116,Fanconi Syndrome
+BMGC_DS00861,BMG_DS001117,Fanconi Anemia
+BMGC_DS00862,BMG_DS001119,Farmer's Lung
+BMGC_DS00863,BMG_DS001120,Fascicular Block
+BMGC_DS00864,BMG_DS001121,Fasciitis
+BMGC_DS00865,BMG_DS001122,Fascioliasis
+BMGC_DS00866,BMG_DS001123,Fascioloidiasis
+BMGC_DS00867,BMG_DS001124,Fasciolopsiasis
+BMGC_DS00868,BMG_DS001125,Chronic Fatigue Syndrome
+BMGC_DS00869,BMG_DS001126,Fatty Liver
+BMGC_DS00870,BMG_DS001127,"Fatty Liver, Alcoholic"
+BMGC_DS00871,BMG_DS001128,Favism
+BMGC_DS00872,BMG_DS001129,Favre-Racouchot Syndrome
+BMGC_DS00873,BMG_DS001130,progressive bulbar palsy of childhood
+BMGC_DS00874,BMG_DS001131,Fecal Incontinence
+BMGC_DS00875,BMG_DS001133,Felty Syndrome
+BMGC_DS00876,BMG_DS001134,neoplasm of femur
+BMGC_DS00877,BMG_DS001135,Femur Head Necrosis
+BMGC_DS00878,BMG_DS001136,Fetal Alcohol Syndrome
+BMGC_DS00879,BMG_DS001137,Fetal Diseases
+BMGC_DS00880,BMG_DS001139,fetal growth restriction
+BMGC_DS00881,BMG_DS001140,Fetal Resorption
+BMGC_DS00882,BMG_DS001141,fetishistic disorder
+BMGC_DS00883,BMG_DS001144,Breast Fibrocystic Disease
+BMGC_DS00884,BMG_DS001145,Fibrodysplasia Ossificans Progressiva
+BMGC_DS00885,BMG_DS001147,fibroma
+BMGC_DS00886,BMG_DS001148,fibromatosis
+BMGC_DS00887,BMG_DS001149,Fibromuscular Dysplasia
+BMGC_DS00888,BMG_DS001150,Fibromyalgia
+BMGC_DS00889,BMG_DS001151,fibrosarcoma
+BMGC_DS00890,BMG_DS001152,"Fibrous Dysplasia, Monostotic"
+BMGC_DS00891,BMG_DS001153,polyostotic fibrous dysplasia
+BMGC_DS00892,BMG_DS001154,Filariasis
+BMGC_DS00893,BMG_DS001156,pyromania
+BMGC_DS00894,BMG_DS001157,Fish Diseases
+BMGC_DS00895,BMG_DS001158,Anal Fissure
+BMGC_DS00896,BMG_DS001159,flatfoot
+BMGC_DS00897,BMG_DS001160,Focal Dermal Hypoplasia
+BMGC_DS00898,BMG_DS001162,"Epilepsy, Partial, Motor"
+BMGC_DS00899,BMG_DS001163,Folic Acid Deficiency
+BMGC_DS00900,BMG_DS001165,Folliculitis
+BMGC_DS00901,BMG_DS001166,Food Allergy
+BMGC_DS00902,BMG_DS001167,Foot Dermatoses
+BMGC_DS00903,BMG_DS001168,Foot Diseases
+BMGC_DS00904,BMG_DS001171,"Foramen Ovale, Patent"
+BMGC_DS00905,BMG_DS001173,Influenza in Birds
+BMGC_DS00906,BMG_DS001175,Fox Fordyce disease
+BMGC_DS00907,BMG_DS001176,Fragile X Syndrome
+BMGC_DS00908,BMG_DS001178,Freemartinism
+BMGC_DS00909,BMG_DS001179,Friedreich Ataxia
+BMGC_DS00910,BMG_DS001180,Froehlich's Syndrome
+BMGC_DS00911,BMG_DS001181,Frontal Sinusitis
+BMGC_DS00912,BMG_DS001182,hereditary fructose intolerance
+BMGC_DS00913,BMG_DS001184,"Fructose-1,6-Diphosphatase Deficiency"
+BMGC_DS00914,BMG_DS001185,Fuchs Endothelial Dystrophy
+BMGC_DS00915,BMG_DS001186,Fuchs' heterochromic cyclitis
+BMGC_DS00916,BMG_DS001187,Fucosidase Deficiency Disease
+BMGC_DS00917,BMG_DS001188,Functional disorder of intestine
+BMGC_DS00918,BMG_DS001190,Furunculosis
+BMGC_DS00919,BMG_DS001191,"teeth, fused"
+BMGC_DS00920,BMG_DS001193,Galactosemias
+BMGC_DS00921,BMG_DS001194,Gall Bladder Diseases
+BMGC_DS00922,BMG_DS001195,gallbladder neoplasm
+BMGC_DS00923,BMG_DS001197,Gangliosidoses
+BMGC_DS00924,BMG_DS001198,Gangrene
+BMGC_DS00925,BMG_DS001199,Gardner Syndrome
+BMGC_DS00926,BMG_DS001201,Gastric Varix
+BMGC_DS00927,BMG_DS001202,gastrin-producing neuroendocrine tumor
+BMGC_DS00928,BMG_DS001203,Gastritis
+BMGC_DS00929,BMG_DS001204,"Gastritis, Atrophic"
+BMGC_DS00930,BMG_DS001205,"Gastritis, Hypertrophic"
+BMGC_DS00931,BMG_DS001206,Gastroenteritis
+BMGC_DS00932,BMG_DS001207,"Gastroenteritis, Transmissible, of Swine"
+BMGC_DS00933,BMG_DS001208,Gastroesophageal reflux disease
+BMGC_DS00934,BMG_DS001209,Gastrointestinal Diseases
+BMGC_DS00935,BMG_DS001210,gastrointestinal system cancer
+BMGC_DS00936,BMG_DS001211,Gaucher Disease
+BMGC_DS00937,BMG_DS001212,Generalized atherosclerosis
+BMGC_DS00938,BMG_DS001213,Generalized Nonconvulsive Seizure Disorder
+BMGC_DS00939,BMG_DS001215,Geniculate Ganglionitis
+BMGC_DS00940,BMG_DS001216,Herpes Zoster Oticus
+BMGC_DS00941,BMG_DS001217,Female Genital Diseases
+BMGC_DS00942,BMG_DS001218,"Genital Diseases, Male"
+BMGC_DS00943,BMG_DS001219,female reproductive system neoplasm
+BMGC_DS00944,BMG_DS001220,male reproductive system neoplasm
+BMGC_DS00945,BMG_DS001221,Primary genital syphilis
+BMGC_DS00946,BMG_DS001222,Geotrichosis
+BMGC_DS00947,BMG_DS001223,Gerstmann syndrome
+BMGC_DS00948,BMG_DS001224,Gerstmann-Straussler-Scheinker Disease
+BMGC_DS00949,BMG_DS001225,giant cell tumor
+BMGC_DS00950,BMG_DS001226,Angiolymphoid hyperplasia
+BMGC_DS00951,BMG_DS001227,Giardiasis
+BMGC_DS00952,BMG_DS001228,Gigantism
+BMGC_DS00953,BMG_DS001229,Gilbert Disease
+BMGC_DS00954,BMG_DS001230,Gingival Diseases
+BMGC_DS00955,BMG_DS001231,Gingival Hypertrophy
+BMGC_DS00956,BMG_DS001233,gingival recession
+BMGC_DS00957,BMG_DS001234,Gingivitis
+BMGC_DS00958,BMG_DS001235,necrotizing ulcerative gingivitis
+BMGC_DS00959,BMG_DS001238,Glaucoma
+BMGC_DS00960,BMG_DS001239,Angle Closure Glaucoma
+BMGC_DS00961,BMG_DS001240,Primary angle-closure glaucoma
+BMGC_DS00962,BMG_DS001241,"Glaucoma, Neovascular"
+BMGC_DS00963,BMG_DS001242,"Glaucoma, Open-Angle"
+BMGC_DS00964,BMG_DS001243,"Glaucoma, Suspect"
+BMGC_DS00965,BMG_DS001244,glioblastoma
+BMGC_DS00966,BMG_DS001245,glioma
+BMGC_DS00967,BMG_DS001246,glomus tumor
+BMGC_DS00968,BMG_DS001248,Glomerulonephritis
+BMGC_DS00969,BMG_DS001249,IGA Glomerulonephritis
+BMGC_DS00970,BMG_DS001250,"Glomerulonephritis, Membranoproliferative"
+BMGC_DS00971,BMG_DS001251,Membranous glomerulonephritis
+BMGC_DS00972,BMG_DS001252,Focal glomerulosclerosis
+BMGC_DS00973,BMG_DS001255,Glossitis
+BMGC_DS00974,BMG_DS001256,"Glossitis, Benign Migratory"
+BMGC_DS00975,BMG_DS001257,glucagonoma
+BMGC_DS00976,BMG_DS001258,Glycogen Storage Disease
+BMGC_DS00977,BMG_DS001259,Glycogen Storage Disease Type I
+BMGC_DS00978,BMG_DS001260,Glycogen storage disease type II
+BMGC_DS00979,BMG_DS001261,Glycogen Storage Disease Type III
+BMGC_DS00980,BMG_DS001262,Glycogen Storage Disease Type IV
+BMGC_DS00981,BMG_DS001263,Glycogen Storage Disease Type V
+BMGC_DS00982,BMG_DS001264,Glycogen Storage Disease Type VI
+BMGC_DS00983,BMG_DS001265,Glycogen Storage Disease Type VII
+BMGC_DS00984,BMG_DS001266,Glycogen Storage Disease Type VIII
+BMGC_DS00985,BMG_DS001267,renal glycosuria
+BMGC_DS00986,BMG_DS001268,Gnathostomiasis
+BMGC_DS00987,BMG_DS001270,Goiter
+BMGC_DS00988,BMG_DS001271,Endemic goiter
+BMGC_DS00989,BMG_DS001272,Nodular Goiter
+BMGC_DS00990,BMG_DS001273,Substernal goiter
+BMGC_DS00991,BMG_DS001274,"Hypertension, Goldblatt"
+BMGC_DS00992,BMG_DS001275,Gonadal Disorders
+BMGC_DS00993,BMG_DS001276,gonadal dysgenesis
+BMGC_DS00994,BMG_DS001277,"Gonadal Dysgenesis, 46,XY"
+BMGC_DS00995,BMG_DS001278,"Gonadal Dysgenesis, Mixed"
+BMGC_DS00996,BMG_DS001283,Gonorrhea
+BMGC_DS00997,BMG_DS001284,Gout
+BMGC_DS00998,BMG_DS001286,Graft-vs-Host Disease
+BMGC_DS00999,BMG_DS001287,"Granular Dystrophy, Corneal"
+BMGC_DS01000,BMG_DS001288,Granuloma Inguinale
+BMGC_DS01001,BMG_DS001290,nasal cavity and paranasal sinus lethal midline granuloma
+BMGC_DS01002,BMG_DS001291,"Granuloma, Respiratory Tract"
+BMGC_DS01003,BMG_DS001292,Granulomatous Angiitis
+BMGC_DS01004,BMG_DS001293,Chronic granulomatous disease
+BMGC_DS01005,BMG_DS001295,granulosa cell tumor
+BMGC_DS01006,BMG_DS001296,Graves Disease
+BMGC_DS01007,BMG_DS001297,Groenouw's Dystrophies
+BMGC_DS01008,BMG_DS001298,Guillain-Barre Syndrome
+BMGC_DS01009,BMG_DS001299,Gynatresia
+BMGC_DS01010,BMG_DS001300,Gynecomastia
+BMGC_DS01011,BMG_DS001301,Gyrate Atrophy
+BMGC_DS01012,BMG_DS001304,Haemonchiasis
+BMGC_DS01013,BMG_DS001305,Haemophilus Infections
+BMGC_DS01014,BMG_DS001306,Hair Diseases
+BMGC_DS01015,BMG_DS001308,Hallermann's Syndrome
+BMGC_DS01016,BMG_DS001309,Hallervorden-Spatz Syndrome
+BMGC_DS01017,BMG_DS001310,hallucinogen abuse
+BMGC_DS01018,BMG_DS001311,hallucinogen dependence
+BMGC_DS01019,BMG_DS001313,hamartoma
+BMGC_DS01020,BMG_DS001314,Cowden disease
+BMGC_DS01021,BMG_DS001315,Hand Dermatoses
+BMGC_DS01022,BMG_DS001316,"Hand, Foot and Mouth Disease"
+BMGC_DS01023,BMG_DS001317,Hartnup Disease
+BMGC_DS01024,BMG_DS001318,Hashish Abuse
+BMGC_DS01025,BMG_DS001319,Hay fever
+BMGC_DS01026,BMG_DS001320,head and neck neoplasm
+BMGC_DS01027,BMG_DS001321,"Hearing Loss, Bilateral"
+BMGC_DS01028,BMG_DS001323,Conductive hearing loss
+BMGC_DS01029,BMG_DS001324,"Hearing Loss, High-Frequency"
+BMGC_DS01030,BMG_DS001325,noise induced hearing loss
+BMGC_DS01031,BMG_DS001326,sensorineural hearing loss disorder
+BMGC_DS01032,BMG_DS001327,Heart Aneurysm
+BMGC_DS01033,BMG_DS001328,Cardiac Arrest
+BMGC_DS01034,BMG_DS001329,Heart Block
+BMGC_DS01035,BMG_DS001330,congenital heart disease
+BMGC_DS01036,BMG_DS001331,Heart Diseases
+BMGC_DS01037,BMG_DS001332,Heart failure
+BMGC_DS01038,BMG_DS001333,Congestive heart failure
+BMGC_DS01039,BMG_DS001334,heart neoplasm
+BMGC_DS01040,BMG_DS001336,"Heart Rupture, Post-Infarction"
+BMGC_DS01041,BMG_DS001337,heart septal defect
+BMGC_DS01042,BMG_DS001338,atrial septal defect
+BMGC_DS01043,BMG_DS001339,ventricular septal defect
+BMGC_DS01044,BMG_DS001340,Heart valve disease
+BMGC_DS01045,BMG_DS001342,heavy chain disease
+BMGC_DS01046,BMG_DS001343,gamma-heavy chain disease
+BMGC_DS01047,BMG_DS001345,Helminthiasis
+BMGC_DS01048,BMG_DS001346,"Helminthiasis, Animal"
+BMGC_DS01049,BMG_DS001348,hemangioma
+BMGC_DS01050,BMG_DS001349,cavernous hemangioma
+BMGC_DS01051,BMG_DS001350,hemangiopericytoma
+BMGC_DS01052,BMG_DS001351,angiosarcoma
+BMGC_DS01053,BMG_DS001352,hemarthrosis
+BMGC_DS01054,BMG_DS001354,Hematocele of tunica vaginalis testis
+BMGC_DS01055,BMG_DS001355,Hematochezia
+BMGC_DS01056,BMG_DS001357,Hematological Disease
+BMGC_DS01057,BMG_DS001358,hemometra
+BMGC_DS01058,BMG_DS001359,Hematomyelia
+BMGC_DS01059,BMG_DS001361,Hematuria
+BMGC_DS01060,BMG_DS001362,Hemeralopia
+BMGC_DS01061,BMG_DS001365,hemiplegia
+BMGC_DS01062,BMG_DS001366,Biliary Tract Hemorrhage
+BMGC_DS01063,BMG_DS001367,Hemochromatosis
+BMGC_DS01064,BMG_DS001368,Hemoglobin C Disease
+BMGC_DS01065,BMG_DS001369,Hemoglobin F Disease
+BMGC_DS01066,BMG_DS001370,Hemoglobin SC Disease
+BMGC_DS01067,BMG_DS001371,Hemoglobinopathies
+BMGC_DS01068,BMG_DS001372,hemoglobinuria
+BMGC_DS01069,BMG_DS001374,"Hemoglobinuria, Paroxysmal"
+BMGC_DS01070,BMG_DS001375,Hemolytic-Uremic Syndrome
+BMGC_DS01071,BMG_DS001376,hemopericardium
+BMGC_DS01072,BMG_DS001377,Reactive Hemophagocytic Syndrome
+BMGC_DS01073,BMG_DS001378,Hemophilia A
+BMGC_DS01074,BMG_DS001379,Hemopneumothorax
+BMGC_DS01075,BMG_DS001380,Hemorrhagic Disorders
+BMGC_DS01076,BMG_DS001381,Hemorrhagic Disease of Newborn
+BMGC_DS01077,BMG_DS001384,"Hemorrhagic Fever, Crimean"
+BMGC_DS01078,BMG_DS001385,Severe Dengue
+BMGC_DS01079,BMG_DS001386,Hemorrhagic Fever with Renal Syndrome
+BMGC_DS01080,BMG_DS001387,"Hemorrhagic Fever, Omsk"
+BMGC_DS01081,BMG_DS001389,Hemorrhoids
+BMGC_DS01082,BMG_DS001390,Hemosiderosis
+BMGC_DS01083,BMG_DS001392,Hepatic Coma
+BMGC_DS01084,BMG_DS001393,Hepatic Encephalopathy
+BMGC_DS01085,BMG_DS001394,Hepatic Vein Thrombosis
+BMGC_DS01086,BMG_DS001395,Hepatic Veno-Occlusive Disease
+BMGC_DS01087,BMG_DS001396,Hepatitis
+BMGC_DS01088,BMG_DS001397,Hepatitis A
+BMGC_DS01089,BMG_DS001398,Hepatitis B
+BMGC_DS01090,BMG_DS001399,"Hepatitis, Alcoholic"
+BMGC_DS01091,BMG_DS001400,"Hepatitis, Animal"
+BMGC_DS01092,BMG_DS001401,"Hepatitis, Chronic"
+BMGC_DS01093,BMG_DS001403,"Hepatitis, Viral, Animal"
+BMGC_DS01094,BMG_DS001404,"Hepatitis, Viral, Human"
+BMGC_DS01095,BMG_DS001405,Hepatitis C
+BMGC_DS01096,BMG_DS001406,Hepatolenticular Degeneration
+BMGC_DS01097,BMG_DS001407,Hepatorenal Syndrome
+BMGC_DS01098,BMG_DS001408,"Angioedemas, Hereditary"
+BMGC_DS01099,BMG_DS001409,Hereditary Diseases
+BMGC_DS01100,BMG_DS001411,hermaphroditism
+BMGC_DS01101,BMG_DS001412,congenital diaphragmatic hernia
+BMGC_DS01102,BMG_DS001413,inguinal hernia
+BMGC_DS01103,BMG_DS001414,"Inguinal Hernia, Direct"
+BMGC_DS01104,BMG_DS001415,inguinal hernia
+BMGC_DS01105,BMG_DS001418,heroin dependence
+BMGC_DS01106,BMG_DS001419,Herpangina
+BMGC_DS01107,BMG_DS001420,Genital Herpes
+BMGC_DS01108,BMG_DS001422,Herpes Labialis
+BMGC_DS01109,BMG_DS001423,Herpes simplex infection
+BMGC_DS01110,BMG_DS001424,"Keratitis, Herpetic"
+BMGC_DS01111,BMG_DS001426,Herpes zoster (disorder)
+BMGC_DS01112,BMG_DS001428,Herpes Zoster Ophthalmicus
+BMGC_DS01113,BMG_DS001429,Herpes zoster without mention of complication
+BMGC_DS01114,BMG_DS001430,Herpesviridae Infections
+BMGC_DS01115,BMG_DS001433,"Deficiency, Hexosediphosphatase"
+BMGC_DS01116,BMG_DS001434,sweat gland adenoma
+BMGC_DS01117,BMG_DS001435,High Pressure Neurological Syndrome
+BMGC_DS01118,BMG_DS001438,von Hippel-Lindau disease
+BMGC_DS01119,BMG_DS001439,Hirschsprung Disease
+BMGC_DS01120,BMG_DS001441,Hirsutism
+BMGC_DS01121,BMG_DS001442,Leech infestation
+BMGC_DS01122,BMG_DS001443,malignant histiocytic disease
+BMGC_DS01123,BMG_DS001444,histiocytosis
+BMGC_DS01124,BMG_DS001445,Langerhans cell histiocytosis
+BMGC_DS01125,BMG_DS001447,"Histiocytosis, Non-Langerhans-Cell"
+BMGC_DS01126,BMG_DS001448,sinus histiocytosis with massive lymphadenopathy
+BMGC_DS01127,BMG_DS001449,Histomoniasis
+BMGC_DS01128,BMG_DS001450,Histoplasmosis
+BMGC_DS01129,BMG_DS001451,histrionic personality disorder
+BMGC_DS01130,BMG_DS001452,HIV Infections
+BMGC_DS01131,BMG_DS001453,"Hereditary, Type VII, Motor and Sensory Neuropathy"
+BMGC_DS01132,BMG_DS001454,classic Hodgkin lymphoma
+BMGC_DS01133,BMG_DS001456,Homocystinuria
+BMGC_DS01134,BMG_DS001457,Hookworm Infections
+BMGC_DS01135,BMG_DS001458,Hordeolum
+BMGC_DS01136,BMG_DS001460,Hordeolum externum
+BMGC_DS01137,BMG_DS001461,Horner Syndrome
+BMGC_DS01138,BMG_DS001462,Horse Diseases
+BMGC_DS01139,BMG_DS001463,"Hereditary Sensory Autonomic Neuropathy, Type 1"
+BMGC_DS01140,BMG_DS001464,"Hereditary Sensory Autonomic Neuropathy, Type 2"
+BMGC_DS01141,BMG_DS001465,HSAN Type IV
+BMGC_DS01142,BMG_DS001466,"Hereditary Sensory Autonomic Neuropathy, Type 5"
+BMGC_DS01143,BMG_DS001468,HTLV-I Infections
+BMGC_DS01144,BMG_DS001470,Huntington Disease
+BMGC_DS01145,BMG_DS001471,Hyaline Membrane Disease
+BMGC_DS01146,BMG_DS001472,hydatidiform mole
+BMGC_DS01147,BMG_DS001473,polyhydramnios
+BMGC_DS01148,BMG_DS001474,hydranencephaly
+BMGC_DS01149,BMG_DS001475,Hydroa Vacciniforme
+BMGC_DS01150,BMG_DS001476,Hydrocephalus
+BMGC_DS01151,BMG_DS001477,congenital hydrocephalus
+BMGC_DS01152,BMG_DS001478,"Hydrocephalus, Normal Pressure"
+BMGC_DS01153,BMG_DS001479,Hydronephrosis
+BMGC_DS01154,BMG_DS001480,congenital glaucoma
+BMGC_DS01155,BMG_DS001481,Hydrops Fetalis
+BMGC_DS01156,BMG_DS001482,Hydrothorax
+BMGC_DS01157,BMG_DS001483,Hymenolepiasis
+BMGC_DS01158,BMG_DS001484,Hyperaldosteronism
+BMGC_DS01159,BMG_DS001485,Hyperbilirubinemia
+BMGC_DS01160,BMG_DS001486,"Hyperbilirubinemia, Hereditary"
+BMGC_DS01161,BMG_DS001487,Hypercalcemia
+BMGC_DS01162,BMG_DS001488,Hypercementosis
+BMGC_DS01163,BMG_DS001489,Hypercholesterolemia
+BMGC_DS01164,BMG_DS001490,"Hypercholesterolemia, Familial"
+BMGC_DS01165,BMG_DS001491,hyperemesis gravidarum
+BMGC_DS01166,BMG_DS001493,Hyperemia
+BMGC_DS01167,BMG_DS001495,Hypergammaglobulinemia
+BMGC_DS01168,BMG_DS001496,Hyperglycemia
+BMGC_DS01169,BMG_DS001497,Hyperglycemic Hyperosmolar Nonketotic Coma
+BMGC_DS01170,BMG_DS001498,Hyperinsulinism
+BMGC_DS01171,BMG_DS001499,Hyperlipidemia
+BMGC_DS01172,BMG_DS001500,"Hyperlipidemia, Familial Combined"
+BMGC_DS01173,BMG_DS001501,Hyperlipoproteinemias
+BMGC_DS01174,BMG_DS001502,Hyperlipoproteinemia Type III
+BMGC_DS01175,BMG_DS001503,Hyperlipoproteinemia Type IV
+BMGC_DS01176,BMG_DS001504,Hyperlipoproteinemia Type V
+BMGC_DS01177,BMG_DS001505,Hypernatremia
+BMGC_DS01178,BMG_DS001506,Hyperopia
+BMGC_DS01179,BMG_DS001507,Hyperostosis
+BMGC_DS01180,BMG_DS001509,Hyperostosis of skull
+BMGC_DS01181,BMG_DS001510,Cortical Congenital Hyperostosis
+BMGC_DS01182,BMG_DS001511,"Hyperostosis, Diffuse Idiopathic Skeletal"
+BMGC_DS01183,BMG_DS001513,Hyperoxaluria
+BMGC_DS01184,BMG_DS001514,Primary Hyperoxaluria
+BMGC_DS01185,BMG_DS001515,Hyperparathyroidism
+BMGC_DS01186,BMG_DS001516,"Hyperparathyroidism, Secondary"
+BMGC_DS01187,BMG_DS001517,Hyperpituitarism
+BMGC_DS01188,BMG_DS001518,hyperplasia
+BMGC_DS01189,BMG_DS001519,Hyperprolactinemia
+BMGC_DS01190,BMG_DS001520,allergic disease
+BMGC_DS01191,BMG_DS001521,type IV hypersensitivity disease
+BMGC_DS01192,BMG_DS001522,Hypersomnia with Periodic Respiration
+BMGC_DS01193,BMG_DS001523,Hypersplenism
+BMGC_DS01194,BMG_DS001524,Hypertensive disease
+BMGC_DS01195,BMG_DS001525,Malignant Hypertension
+BMGC_DS01196,BMG_DS001526,Portal Hypertension
+BMGC_DS01197,BMG_DS001527,pulmonary hypertension
+BMGC_DS01198,BMG_DS001528,Renal hypertension
+BMGC_DS01199,BMG_DS001529,"Hypertension, Renovascular"
+BMGC_DS01200,BMG_DS001530,Hyperthyroidism
+BMGC_DS01201,BMG_DS001531,Hyperthyroxinemia
+BMGC_DS01202,BMG_DS001532,Hypertrichosis
+BMGC_DS01203,BMG_DS001533,Hypertriglyceridemia
+BMGC_DS01204,BMG_DS001534,Hypertrophic elongation of cervix
+BMGC_DS01205,BMG_DS001535,hypertrophy of breast
+BMGC_DS01206,BMG_DS001536,Hypertropia
+BMGC_DS01207,BMG_DS001537,Hypervitaminosis A
+BMGC_DS01208,BMG_DS001539,hypoactive sexual desire disorder
+BMGC_DS01209,BMG_DS001540,Hypoaldosteronism
+BMGC_DS01210,BMG_DS001541,Hypobetalipoproteinemias
+BMGC_DS01211,BMG_DS001542,Hypocalcemia
+BMGC_DS01212,BMG_DS001543,Hypocalciuria
+BMGC_DS01213,BMG_DS001544,hypochondriasis
+BMGC_DS01214,BMG_DS001545,Hypodermyiasis
+BMGC_DS01215,BMG_DS001546,tooth agenesis
+BMGC_DS01216,BMG_DS001547,Hypogalactia
+BMGC_DS01217,BMG_DS001548,Hypoglycemia
+BMGC_DS01218,BMG_DS001549,Hypoglycemic coma
+BMGC_DS01219,BMG_DS001550,Hypogonadism
+BMGC_DS01220,BMG_DS001551,Hypohidrosis
+BMGC_DS01221,BMG_DS001552,hypolipoproteinemia
+BMGC_DS01222,BMG_DS001553,Hypomenorrhea
+BMGC_DS01223,BMG_DS001554,Hyponatremia
+BMGC_DS01224,BMG_DS001555,Hypoparathyroidism
+BMGC_DS01225,BMG_DS001557,Hypophosphatasia
+BMGC_DS01226,BMG_DS001559,Hypopituitarism
+BMGC_DS01227,BMG_DS001560,Hypoproteinemia
+BMGC_DS01228,BMG_DS001561,Hypopyon
+BMGC_DS01229,BMG_DS001562,hypotensive disorder
+BMGC_DS01230,BMG_DS001563,"Hypotension, Orthostatic"
+BMGC_DS01231,BMG_DS001564,Hypothalamic Diseases
+BMGC_DS01232,BMG_DS001565,hypothalamic neoplasm
+BMGC_DS01233,BMG_DS001566,Hypothyroidism
+BMGC_DS01234,BMG_DS001567,Hypotrichosis
+BMGC_DS01235,BMG_DS001569,Type II Mucolipidosis
+BMGC_DS01236,BMG_DS001570,Iatrogenic Disease
+BMGC_DS01237,BMG_DS001571,Ichthyoses
+BMGC_DS01238,BMG_DS001572,Congenital ichthyosis
+BMGC_DS01239,BMG_DS001573,Idiopathic Hypercatabolic Hypoproteinemia
+BMGC_DS01240,BMG_DS001574,Idiopathic pulmonary hemosiderosis
+BMGC_DS01241,BMG_DS001576,ileal neoplasm
+BMGC_DS01242,BMG_DS001577,Ileitis
+BMGC_DS01243,BMG_DS001578,Immune Complex Diseases
+BMGC_DS01244,BMG_DS001579,angioimmunoblastic T-cell lymphoma
+BMGC_DS01245,BMG_DS001580,Immunologic Deficiency Syndromes
+BMGC_DS01246,BMG_DS001581,Immune System Diseases
+BMGC_DS01247,BMG_DS001582,immunoproliferative disorder
+BMGC_DS01248,BMG_DS001584,Impetigo
+BMGC_DS01249,BMG_DS001586,impulse control disorder
+BMGC_DS01250,BMG_DS001587,Inappropriate ADH Syndrome
+BMGC_DS01251,BMG_DS001589,incontinentia pigmenti
+BMGC_DS01252,BMG_DS001590,Indeterminate leprosy
+BMGC_DS01253,BMG_DS001591,pseudohermaphroditism
+BMGC_DS01254,BMG_DS001592,Infant Nutrition Disorders
+BMGC_DS01255,BMG_DS001593,Neonatal disorder
+BMGC_DS01256,BMG_DS001594,"Infant, Premature, Diseases"
+BMGC_DS01257,BMG_DS001595,Infection of kidney
+BMGC_DS01258,BMG_DS001597,Infectious enteritis
+BMGC_DS01259,BMG_DS001598,Infectious Mononucleosis
+BMGC_DS01260,BMG_DS001599,Infective otitis externa
+BMGC_DS01261,BMG_DS001600,infertility disorder
+BMGC_DS01262,BMG_DS001601,Infertility due to extratesticular cause
+BMGC_DS01263,BMG_DS001602,female infertility
+BMGC_DS01264,BMG_DS001603,Male infertility
+BMGC_DS01265,BMG_DS001604,Inflammatory Bowel Diseases
+BMGC_DS01266,BMG_DS001605,inflammatory spondylopathy
+BMGC_DS01267,BMG_DS001606,Influenza
+BMGC_DS01268,BMG_DS001608,infratentorial neoplasm
+BMGC_DS01269,BMG_DS001609,Disorders of Environmental Origin
+BMGC_DS01270,BMG_DS001611,Sleep Initiation and Maintenance Disorders
+BMGC_DS01271,BMG_DS001613,pancreatic insulinoma
+BMGC_DS01272,BMG_DS001614,Intermittent Claudication
+BMGC_DS01273,BMG_DS001615,intermittent explosive disorder
+BMGC_DS01274,BMG_DS001617,Intervertebral Disk Displacement
+BMGC_DS01275,BMG_DS001619,Intestinal Atresia
+BMGC_DS01276,BMG_DS001620,intestinal disaccharidase deficiency
+BMGC_DS01277,BMG_DS001621,Intestinal Diseases
+BMGC_DS01278,BMG_DS001622,"Intestinal Diseases, Parasitic"
+BMGC_DS01279,BMG_DS001624,intestinal neoplasm
+BMGC_DS01280,BMG_DS001625,Intestinal Obstruction
+BMGC_DS01281,BMG_DS001626,Intestinal Perforation
+BMGC_DS01282,BMG_DS001627,intestinal polyp
+BMGC_DS01283,BMG_DS001628,Intestinal Pseudo-Obstruction
+BMGC_DS01284,BMG_DS001630,Intracranial abscess
+BMGC_DS01285,BMG_DS001632,Intussusception
+BMGC_DS01286,BMG_DS001637,Iridocyclitis
+BMGC_DS01287,BMG_DS001638,Iris Diseases
+BMGC_DS01288,BMG_DS001639,iris neoplasm
+BMGC_DS01289,BMG_DS001640,Iritis
+BMGC_DS01290,BMG_DS001641,Irritable Bowel Syndrome
+BMGC_DS01291,BMG_DS001642,ischemic disease
+BMGC_DS01292,BMG_DS001644,insulinoma
+BMGC_DS01293,BMG_DS001645,Ito hypomelanosis
+BMGC_DS01294,BMG_DS001646,Jacksonian Seizure
+BMGC_DS01295,BMG_DS001647,Creutzfeldt-Jakob disease
+BMGC_DS01296,BMG_DS001648,Late-Infantile Neuronal Ceroid Lipofuscinosis
+BMGC_DS01297,BMG_DS001649,"Jaundice, Chronic Idiopathic"
+BMGC_DS01298,BMG_DS001650,neonatal jaundice
+BMGC_DS01299,BMG_DS001651,"Jaundice, Obstructive"
+BMGC_DS01300,BMG_DS001652,Jaw Diseases
+BMGC_DS01301,BMG_DS001653,neoplasm of jaw
+BMGC_DS01302,BMG_DS001656,Jejunal Diseases
+BMGC_DS01303,BMG_DS001657,jejunal neoplasm
+BMGC_DS01304,BMG_DS001658,Jervell-Lange Nielsen Syndrome
+BMGC_DS01305,BMG_DS001659,Arthropathy
+BMGC_DS01306,BMG_DS001661,Juvenile osteochondrosis of hip AND/OR pelvis
+BMGC_DS01307,BMG_DS001663,Kartagener Syndrome
+BMGC_DS01308,BMG_DS001664,Kearns-Sayre syndrome
+BMGC_DS01309,BMG_DS001665,keloid
+BMGC_DS01310,BMG_DS001666,Keratitis
+BMGC_DS01311,BMG_DS001667,"Keratitis, Dendritic"
+BMGC_DS01312,BMG_DS001668,keratoacanthoma
+BMGC_DS01313,BMG_DS001669,Keratoconjunctivitis
+BMGC_DS01314,BMG_DS001670,Keratoconjunctivitis Sicca
+BMGC_DS01315,BMG_DS001672,"Keratoconjunctivitis, Vernal"
+BMGC_DS01316,BMG_DS001673,Keratoconus
+BMGC_DS01317,BMG_DS001675,acquired keratosis
+BMGC_DS01318,BMG_DS001676,"Keratoderma, Palmoplantar, Diffuse"
+BMGC_DS01319,BMG_DS001677,Keratosis
+BMGC_DS01320,BMG_DS001678,Keratosis Blennorrhagica
+BMGC_DS01321,BMG_DS001679,Keratosis Follicularis
+BMGC_DS01322,BMG_DS001680,palmoplantar keratosis
+BMGC_DS01323,BMG_DS001681,actinic keratosis
+BMGC_DS01324,BMG_DS001682,seborrheic keratosis
+BMGC_DS01325,BMG_DS001683,Kernicterus
+BMGC_DS01326,BMG_DS001685,Kidney Cortex Necrosis
+BMGC_DS01327,BMG_DS001686,Kidney Diseases
+BMGC_DS01328,BMG_DS001687,"Kidney Failure, Acute"
+BMGC_DS01329,BMG_DS001688,"Kidney Failure, Chronic"
+BMGC_DS01330,BMG_DS001689,kidney neoplasm
+BMGC_DS01331,BMG_DS001690,Kidney Papillary Necrosis
+BMGC_DS01332,BMG_DS001691,Acute Kidney Tubular Necrosis
+BMGC_DS01333,BMG_DS001692,Cystic kidney
+BMGC_DS01334,BMG_DS001693,Polycystic Kidney Diseases
+BMGC_DS01335,BMG_DS001694,Medullary sponge kidney
+BMGC_DS01336,BMG_DS001695,Kienbock Disease
+BMGC_DS01337,BMG_DS001696,Menkes Kinky Hair Syndrome
+BMGC_DS01338,BMG_DS001697,Klebsiella Infections
+BMGC_DS01339,BMG_DS001698,kleptomania
+BMGC_DS01340,BMG_DS001699,Klinefelter Syndrome
+BMGC_DS01341,BMG_DS001700,Klippel-Feil Syndrome
+BMGC_DS01342,BMG_DS001701,Klippel-Trenaunay-Weber Syndrome
+BMGC_DS01343,BMG_DS001702,leukoplakia of penis
+BMGC_DS01344,BMG_DS001703,Vulvar Lichen Sclerosus
+BMGC_DS01345,BMG_DS001704,Krukenberg carcinoma
+BMGC_DS01346,BMG_DS001705,Adult Neuronal Ceroid Lipofuscinosis
+BMGC_DS01347,BMG_DS001706,Kuru
+BMGC_DS01348,BMG_DS001707,Kwashiorkor
+BMGC_DS01349,BMG_DS001708,Kyasanur Forest Disease
+BMGC_DS01350,BMG_DS001710,Labyrinthine disorder
+BMGC_DS01351,BMG_DS001711,Labyrinthitis
+BMGC_DS01352,BMG_DS001712,Lacrimal Apparatus Diseases
+BMGC_DS01353,BMG_DS001713,lacrimal duct obstruction
+BMGC_DS01354,BMG_DS001714,Lactation Disorder
+BMGC_DS01355,BMG_DS001715,Lactose Intolerance
+BMGC_DS01356,BMG_DS001717,Lambert-Eaton Myasthenic Syndrome
+BMGC_DS01357,BMG_DS001719,Langer-Giedion Syndrome
+BMGC_DS01358,BMG_DS001721,language disorder
+BMGC_DS01359,BMG_DS001723,"Larva Migrans, Visceral"
+BMGC_DS01360,BMG_DS001724,Laryngeal Diseases
+BMGC_DS01361,BMG_DS001725,laryngeal neoplasm
+BMGC_DS01362,BMG_DS001726,Laryngeal Perichondritis
+BMGC_DS01363,BMG_DS001727,Laryngospasm
+BMGC_DS01364,BMG_DS001728,Laryngitis
+BMGC_DS01365,BMG_DS001730,laryngostenosis
+BMGC_DS01366,BMG_DS001733,Lassa Fever
+BMGC_DS01367,BMG_DS001734,Laurence-Moon Syndrome
+BMGC_DS01368,BMG_DS001736,learning disability
+BMGC_DS01369,BMG_DS001737,Familial lecithin cholesterol acyltransferase deficiency
+BMGC_DS01370,BMG_DS001738,Left Bundle-Branch Block
+BMGC_DS01371,BMG_DS001739,Left-Sided Heart Failure
+BMGC_DS01372,BMG_DS001741,Leg Dermatoses
+BMGC_DS01373,BMG_DS001742,Leg Ulcer
+BMGC_DS01374,BMG_DS001743,Coxa plana (disorder)
+BMGC_DS01375,BMG_DS001744,Legionellosis
+BMGC_DS01376,BMG_DS001745,Legionnaires' Disease
+BMGC_DS01377,BMG_DS001746,Leigh Disease
+BMGC_DS01378,BMG_DS001747,leiomyoma
+BMGC_DS01379,BMG_DS001748,leiomyosarcoma
+BMGC_DS01380,BMG_DS001749,Leishmaniasis
+BMGC_DS01381,BMG_DS001750,"Leishmaniasis, Cutaneous"
+BMGC_DS01382,BMG_DS001755,"Leishmaniasis, Visceral"
+BMGC_DS01383,BMG_DS001756,Lens Diseases
+BMGC_DS01384,BMG_DS001757,Lens Dislocation and Subluxation
+BMGC_DS01385,BMG_DS001758,Lens Subluxation
+BMGC_DS01386,BMG_DS001759,Lentigo
+BMGC_DS01387,BMG_DS001760,Leprosy
+BMGC_DS01388,BMG_DS001761,Borderline leprosy
+BMGC_DS01389,BMG_DS001762,"Leprosy, Lepromatous"
+BMGC_DS01390,BMG_DS001763,Tuberculoid leprosy
+BMGC_DS01391,BMG_DS001765,Leptospirosis
+BMGC_DS01392,BMG_DS001768,Lesch-Nyhan Syndrome
+BMGC_DS01393,BMG_DS001769,Letterer-Siwe Disease
+BMGC_DS01394,BMG_DS001770,leukemia
+BMGC_DS01395,BMG_DS001771,B-cell chronic lymphocytic leukemia
+BMGC_DS01396,BMG_DS001772,acute basophilic leukemia
+BMGC_DS01397,BMG_DS001773,acute erythroid leukemia
+BMGC_DS01398,BMG_DS001774,hairy cell leukemia
+BMGC_DS01399,BMG_DS001775,lymphoid leukemia
+BMGC_DS01400,BMG_DS001776,acute lymphoblastic leukemia
+BMGC_DS01401,BMG_DS001777,childhood acute lymphoblastic leukemia
+BMGC_DS01402,BMG_DS001778,mast cell leukemia
+BMGC_DS01403,BMG_DS001779,acute megakaryoblastic leukemia
+BMGC_DS01404,BMG_DS001780,acute biphenotypic leukemia
+BMGC_DS01405,BMG_DS001781,acute monocytic leukemia
+BMGC_DS01406,BMG_DS001782,chronic monocytic leukemia
+BMGC_DS01407,BMG_DS001783,acute myeloid leukemia
+BMGC_DS01408,BMG_DS001784,myeloid leukemia
+BMGC_DS01409,BMG_DS001786,"chronic myelogenous leukemia, BCR-ABL1 positive | chronic myeloid leukemia"
+BMGC_DS01410,BMG_DS001788,acute myelomonocytic leukemia M4
+BMGC_DS01411,BMG_DS001789,chronic myelomonocytic leukemia
+BMGC_DS01412,BMG_DS001790,chronic neutrophilic leukemia
+BMGC_DS01413,BMG_DS001791,null-cell leukemia
+BMGC_DS01414,BMG_DS001792,plasma cell leukemia
+BMGC_DS01415,BMG_DS001793,prolymphocytic leukemia
+BMGC_DS01416,BMG_DS001794,acute promyelocytic leukemia
+BMGC_DS01417,BMG_DS001795,T-cell leukemia
+BMGC_DS01418,BMG_DS001796,adult T-cell leukemia/lymphoma
+BMGC_DS01419,BMG_DS001797,Leukemoid Reaction
+BMGC_DS01420,BMG_DS001798,Leukocyte Disorders
+BMGC_DS01421,BMG_DS001799,Leukocytosis
+BMGC_DS01422,BMG_DS001800,Leukodystrophy
+BMGC_DS01423,BMG_DS001801,Krabbe disease
+BMGC_DS01424,BMG_DS001802,"Leukodystrophy, Metachromatic"
+BMGC_DS01425,BMG_DS001803,Oral leukoedema
+BMGC_DS01426,BMG_DS001804,"Leukoencephalopathy, Progressive Multifocal"
+BMGC_DS01427,BMG_DS001806,"Leukomalacia, Periventricular"
+BMGC_DS01428,BMG_DS001807,Leukopenia
+BMGC_DS01429,BMG_DS001808,leukoplakia
+BMGC_DS01430,BMG_DS001809,oral mucosa leukoplakia
+BMGC_DS01431,BMG_DS001810,leukorrhea
+BMGC_DS01432,BMG_DS001813,Leydig cell tumor
+BMGC_DS01433,BMG_DS001814,lichen disease
+BMGC_DS01434,BMG_DS001815,Lichen planus follicularis
+BMGC_DS01435,BMG_DS001816,Lichen Planus
+BMGC_DS01436,BMG_DS001824,linitis plastica
+BMGC_DS01437,BMG_DS001825,Lip Diseases
+BMGC_DS01438,BMG_DS001827,"Lipid Metabolism, Inborn Errors"
+BMGC_DS01439,BMG_DS001828,Mucopolysaccharidosis I
+BMGC_DS01440,BMG_DS001829,Lipodystrophy
+BMGC_DS01441,BMG_DS001830,Whipple Disease
+BMGC_DS01442,BMG_DS001831,Lipoidosis
+BMGC_DS01443,BMG_DS001832,Lipoid Proteinosis of Urbach and Wiethe
+BMGC_DS01444,BMG_DS001833,lipoma
+BMGC_DS01445,BMG_DS001834,Lipomatosis
+BMGC_DS01446,BMG_DS001836,"Lipomatosis, Multiple Symmetrical"
+BMGC_DS01447,BMG_DS001837,Lipomucopolysaccharidosis
+BMGC_DS01448,BMG_DS001838,Hyperlipoproteinemia Type I
+BMGC_DS01449,BMG_DS001839,liposarcoma
+BMGC_DS01450,BMG_DS001840,Listeriosis
+BMGC_DS01451,BMG_DS001841,Little's Disease
+BMGC_DS01452,BMG_DS001842,Liver Abscess
+BMGC_DS01453,BMG_DS001843,"Liver Abscess, Amebic"
+BMGC_DS01454,BMG_DS001844,Liver Cirrhosis
+BMGC_DS01455,BMG_DS001845,"Liver Cirrhosis, Alcoholic"
+BMGC_DS01456,BMG_DS001846,Biliary cirrhosis
+BMGC_DS01457,BMG_DS001847,liver disease
+BMGC_DS01458,BMG_DS001848,Alcoholic Liver Diseases
+BMGC_DS01459,BMG_DS001849,"Liver Diseases, Parasitic"
+BMGC_DS01460,BMG_DS001850,liver cancer
+BMGC_DS01461,BMG_DS001851,Lobstein Disease
+BMGC_DS01462,BMG_DS001853,Locked-In Syndrome
+BMGC_DS01463,BMG_DS001854,loiasis
+BMGC_DS01464,BMG_DS001855,long QT syndrome
+BMGC_DS01465,BMG_DS001856,louping ill
+BMGC_DS01466,BMG_DS001857,Lown-Ganong-Levine syndrome
+BMGC_DS01467,BMG_DS001858,Ludwig's angina
+BMGC_DS01468,BMG_DS001860,lung abscess
+BMGC_DS01469,BMG_DS001861,Lung diseases
+BMGC_DS01470,BMG_DS001862,"Lung Diseases, Fungal"
+BMGC_DS01471,BMG_DS001863,Chronic Obstructive Airway Disease
+BMGC_DS01472,BMG_DS001864,"Lung Diseases, Parasitic"
+BMGC_DS01473,BMG_DS001865,lung neoplasm
+BMGC_DS01474,BMG_DS001867,"Lupus Erythematosus, Cutaneous"
+BMGC_DS01475,BMG_DS001868,Chronic discoid lupus erythematosus
+BMGC_DS01476,BMG_DS001869,"Lupus Erythematosus, Subacute Cutaneous"
+BMGC_DS01477,BMG_DS001870,"Lupus Erythematosus, Systemic"
+BMGC_DS01478,BMG_DS001871,Lupus Nephritis
+BMGC_DS01479,BMG_DS001872,Chilblain lupus 1
+BMGC_DS01480,BMG_DS001873,Lutembacher Syndrome
+BMGC_DS01481,BMG_DS001874,Lyme Disease
+BMGC_DS01482,BMG_DS001875,Lymphadenitis
+BMGC_DS01483,BMG_DS001876,Lymphangiectasis
+BMGC_DS01484,BMG_DS001879,lymphangioma
+BMGC_DS01485,BMG_DS001882,Lymphangitis
+BMGC_DS01486,BMG_DS001883,Lymphatic Diseases
+BMGC_DS01487,BMG_DS001884,Lymphedema
+BMGC_DS01488,BMG_DS001885,Lymphocele
+BMGC_DS01489,BMG_DS001886,Lymphocytic Choriomeningitis
+BMGC_DS01490,BMG_DS001887,Lymphocytosis
+BMGC_DS01491,BMG_DS001888,Lymphogranuloma Venereum
+BMGC_DS01492,BMG_DS001889,"Lymphohistiocytosis, Hemophagocytic"
+BMGC_DS01493,BMG_DS001890,lymphoma
+BMGC_DS01494,BMG_DS001891,follicular lymphoma
+BMGC_DS01495,BMG_DS001892,reticulum cell sarcoma
+BMGC_DS01496,BMG_DS001893,non-Hodgkin lymphoma
+BMGC_DS01497,BMG_DS001894,lymphomatoid granulomatosis
+BMGC_DS01498,BMG_DS001895,Lymphopenia
+BMGC_DS01499,BMG_DS001896,lymphoproliferative syndrome
+BMGC_DS01500,BMG_DS001897,Machado-Joseph Disease
+BMGC_DS01501,BMG_DS001898,Waldenstrom macroglobulinemia
+BMGC_DS01502,BMG_DS001899,Macroglossia
+BMGC_DS01503,BMG_DS001900,Macular degeneration
+BMGC_DS01504,BMG_DS001901,Macular corneal dystrophy
+BMGC_DS01505,BMG_DS001902,"Macular Edema, Cystoid"
+BMGC_DS01506,BMG_DS001903,Macular Holes
+BMGC_DS01507,BMG_DS001904,Mycetoma
+BMGC_DS01508,BMG_DS001905,Maffucci Syndrome
+BMGC_DS01509,BMG_DS001906,Magnesium Deficiency
+BMGC_DS01510,BMG_DS001907,Majewski Syndrome
+BMGC_DS01511,BMG_DS001908,major depressive disorder
+BMGC_DS01512,BMG_DS001909,Malabsorption Syndrome
+BMGC_DS01513,BMG_DS001911,Malaria
+BMGC_DS01514,BMG_DS001913,"Malaria, Cerebral"
+BMGC_DS01515,BMG_DS001914,"Malaria, Falciparum"
+BMGC_DS01516,BMG_DS001915,Quartan malaria
+BMGC_DS01517,BMG_DS001916,"Malaria, Vivax"
+BMGC_DS01518,BMG_DS001917,Malignant Carcinoid Syndrome
+BMGC_DS01519,BMG_DS001918,Malignant essential hypertension
+BMGC_DS01520,BMG_DS001919,malignant hyperthermia of anesthesia
+BMGC_DS01521,BMG_DS001920,liver cancer
+BMGC_DS01522,BMG_DS001922,retinal cancer
+BMGC_DS01523,BMG_DS001923,gastric cancer
+BMGC_DS01524,BMG_DS001924,lung cancer
+BMGC_DS01525,BMG_DS001926,Mandibular Diseases
+BMGC_DS01526,BMG_DS001927,mandibular cancer
+BMGC_DS01527,BMG_DS001928,Mange
+BMGC_DS01528,BMG_DS001929,"Mange, Sarcoptic"
+BMGC_DS01529,BMG_DS001930,manic bipolar affective disorder
+BMGC_DS01530,BMG_DS001931,alpha-Mannosidosis
+BMGC_DS01531,BMG_DS001932,Mansonelliasis
+BMGC_DS01532,BMG_DS001933,Maple Syrup Urine Disease
+BMGC_DS01533,BMG_DS001934,Marburg Virus Disease
+BMGC_DS01534,BMG_DS001935,Paroxysmal nocturnal hemoglobinuria
+BMGC_DS01535,BMG_DS001936,Marfan Syndrome
+BMGC_DS01536,BMG_DS001938,cannabis abuse
+BMGC_DS01537,BMG_DS001939,Marinesco-Sjogren syndrome
+BMGC_DS01538,BMG_DS001940,Mastitis
+BMGC_DS01539,BMG_DS001943,mastocytosis
+BMGC_DS01540,BMG_DS001944,"Mastocytosis, Bullous"
+BMGC_DS01541,BMG_DS001945,diffuse cutaneous mastocytosis
+BMGC_DS01542,BMG_DS001946,Mastoiditis
+BMGC_DS01543,BMG_DS001947,Maxillary Diseases
+BMGC_DS01544,BMG_DS001948,maxillary neoplasm
+BMGC_DS01545,BMG_DS001949,maxillary sinus neoplasm
+BMGC_DS01546,BMG_DS001950,Maxillary Sinusitis
+BMGC_DS01547,BMG_DS001951,Measles
+BMGC_DS01548,BMG_DS001952,Meckel diverticulum
+BMGC_DS01549,BMG_DS001953,Meconium Aspiration Syndrome
+BMGC_DS01550,BMG_DS001956,Mediastinal Emphysema
+BMGC_DS01551,BMG_DS001957,neoplasm of mediastinum
+BMGC_DS01552,BMG_DS001958,Mediastinitis
+BMGC_DS01553,BMG_DS001959,medulloblastoma
+BMGC_DS01554,BMG_DS001960,megacolon
+BMGC_DS01555,BMG_DS001961,"Megacolon, Toxic"
+BMGC_DS01556,BMG_DS001962,Megaesophagus
+BMGC_DS01557,BMG_DS001963,Meige Syndrome
+BMGC_DS01558,BMG_DS001965,melancholia
+BMGC_DS01559,BMG_DS001966,melanoma
+BMGC_DS01560,BMG_DS001967,Melanosis
+BMGC_DS01561,BMG_DS001969,Chloasma
+BMGC_DS01562,BMG_DS001970,Meleda Disease
+BMGC_DS01563,BMG_DS001971,Melioidosis
+BMGC_DS01564,BMG_DS001972,Melkersson-Rosenthal Syndrome
+BMGC_DS01565,BMG_DS001973,Melnick-Needles Syndrome
+BMGC_DS01566,BMG_DS001974,Melorheostosis
+BMGC_DS01567,BMG_DS001975,multiple endocrine neoplasia type 1
+BMGC_DS01568,BMG_DS001976,multiple endocrine neoplasia type 2A
+BMGC_DS01569,BMG_DS001977,multiple endocrine neoplasia type 2B
+BMGC_DS01570,BMG_DS001978,Meniere Disease
+BMGC_DS01571,BMG_DS001979,tumor of meninges
+BMGC_DS01572,BMG_DS001980,meningioma
+BMGC_DS01573,BMG_DS001981,Meningitis
+BMGC_DS01574,BMG_DS001982,Aseptic Meningitis
+BMGC_DS01575,BMG_DS001983,"Meningitis, Haemophilus"
+BMGC_DS01576,BMG_DS001984,"Meningitis, Listeria"
+BMGC_DS01577,BMG_DS001985,Meningococcal meningitis
+BMGC_DS01578,BMG_DS001986,"Meningitis, Pneumococcal"
+BMGC_DS01579,BMG_DS001987,Viral meningitis
+BMGC_DS01580,BMG_DS001988,Meningocele
+BMGC_DS01581,BMG_DS001989,Meningococcal Infections
+BMGC_DS01582,BMG_DS001990,Meningococcal Septicemia
+BMGC_DS01583,BMG_DS001991,Meningoencephalitis
+BMGC_DS01584,BMG_DS001994,myelomeningocele
+BMGC_DS01585,BMG_DS001995,Menopausal syndrome
+BMGC_DS01586,BMG_DS001996,Premature Menopause
+BMGC_DS01587,BMG_DS001997,"Menstruation, Retrograde"
+BMGC_DS01588,BMG_DS001998,intellectual disability
+BMGC_DS01589,BMG_DS001999,mesenchymoma
+BMGC_DS01590,BMG_DS002000,Mesenteric Lymphadenitis
+BMGC_DS01591,BMG_DS002002,Mesenteric Vascular Occlusion
+BMGC_DS01592,BMG_DS002003,mesonephric adenocarcinoma
+BMGC_DS01593,BMG_DS002004,mesothelioma
+BMGC_DS01594,BMG_DS002005,Metabolic Diseases
+BMGC_DS01595,BMG_DS002006,Inborn Errors of Metabolism
+BMGC_DS01596,BMG_DS002007,Metagonimiasis
+BMGC_DS01597,BMG_DS002008,"Metal Metabolism, Inborn Errors"
+BMGC_DS01598,BMG_DS002009,Methemoglobinemia
+BMGC_DS01599,BMG_DS002010,"Microangiopathy, Diabetic"
+BMGC_DS01600,BMG_DS002011,isolated congenital microcephaly
+BMGC_DS01601,BMG_DS002012,microphthalmia
+BMGC_DS01602,BMG_DS002013,Middle Lobe Syndrome
+BMGC_DS01603,BMG_DS002014,Mikulicz Disease
+BMGC_DS01604,BMG_DS002015,Miliaria
+BMGC_DS01605,BMG_DS002017,Milk-Alkali Syndrome
+BMGC_DS01606,BMG_DS002018,Milker's Nodes
+BMGC_DS01607,BMG_DS002019,Mite Infestations
+BMGC_DS01608,BMG_DS002020,mitral valve disorder
+BMGC_DS01609,BMG_DS002021,Mitral Valve Insufficiency
+BMGC_DS01610,BMG_DS002022,Mitral Valve Prolapse Syndrome
+BMGC_DS01611,BMG_DS002023,Mitral Valve Stenosis
+BMGC_DS01612,BMG_DS002024,Mixed Connective Tissue Disease
+BMGC_DS01613,BMG_DS002025,pleomorphic adenoma
+BMGC_DS01614,BMG_DS002026,Mohr Syndrome
+BMGC_DS01615,BMG_DS002027,Molluscum Contagiosum
+BMGC_DS01616,BMG_DS002028,Monieziasis
+BMGC_DS01617,BMG_DS002030,monoclonal gammopathy of uncertain significance
+BMGC_DS01618,BMG_DS002031,monoclonal paraproteinemia disease
+BMGC_DS01619,BMG_DS002033,morphine dependence
+BMGC_DS01620,BMG_DS002034,Motion Sickness
+BMGC_DS01621,BMG_DS002035,dental fluorosis
+BMGC_DS01622,BMG_DS002036,Mouth Diseases
+BMGC_DS01623,BMG_DS002037,oral cavity neoplasm
+BMGC_DS01624,BMG_DS002038,Movement Disorders
+BMGC_DS01625,BMG_DS002039,Moyamoya Disease
+BMGC_DS01626,BMG_DS002040,Mucocele of appendix
+BMGC_DS01627,BMG_DS002041,mucocele of salivary gland
+BMGC_DS01628,BMG_DS002042,Mucocutaneous Lymph Node Syndrome
+BMGC_DS01629,BMG_DS002043,Mucolipidoses
+BMGC_DS01630,BMG_DS002044,Mucopolysaccharidoses
+BMGC_DS01631,BMG_DS002045,Mucopolysaccharidosis II
+BMGC_DS01632,BMG_DS002046,Mucopolysaccharidosis III
+BMGC_DS01633,BMG_DS002047,Mucopolysaccharidosis IV
+BMGC_DS01634,BMG_DS002048,Mucopolysaccharidosis V
+BMGC_DS01635,BMG_DS002049,Mucopolysaccharidosis VI
+BMGC_DS01636,BMG_DS002050,Mucormycosis
+BMGC_DS01637,BMG_DS002051,Multiple Carboxylase Deficiency
+BMGC_DS01638,BMG_DS002052,multiple epiphyseal dysplasia
+BMGC_DS01639,BMG_DS002053,plasma cell myeloma
+BMGC_DS01640,BMG_DS002054,Multiple Organ Failure
+BMGC_DS01641,BMG_DS002055,Multiple Sclerosis
+BMGC_DS01642,BMG_DS002056,multiple personality disorder
+BMGC_DS01643,BMG_DS002057,Mumps
+BMGC_DS01644,BMG_DS002058,muscular atrophy
+BMGC_DS01645,BMG_DS002059,Spinal Muscular Atrophy
+BMGC_DS01646,BMG_DS002060,Myopathy
+BMGC_DS01647,BMG_DS002062,Muscular Dystrophy
+BMGC_DS01648,BMG_DS002063,"Muscular Dystrophy, Animal"
+BMGC_DS01649,BMG_DS002064,Musculoskeletal Diseases
+BMGC_DS01650,BMG_DS002065,Mutism
+BMGC_DS01651,BMG_DS002066,Myasthenia Gravis
+BMGC_DS01652,BMG_DS002068,Mycobacterium avium-intracellulare Infection
+BMGC_DS01653,BMG_DS002069,Mycobacterium Infections
+BMGC_DS01654,BMG_DS002070,"Mycobacterium Infections, Nontuberculous"
+BMGC_DS01655,BMG_DS002071,Mycoplasma Infections
+BMGC_DS01656,BMG_DS002073,Mycoses
+BMGC_DS01657,BMG_DS002074,mycosis fungoides
+BMGC_DS01658,BMG_DS002075,Myelitis
+BMGC_DS01659,BMG_DS002076,"Myelitis, Transverse"
+BMGC_DS01660,BMG_DS002077,myelofibrosis
+BMGC_DS01661,BMG_DS002078,acute myeloblastic leukemia without maturation
+BMGC_DS01662,BMG_DS002079,bone marrow cancer
+BMGC_DS01663,BMG_DS002080,Myiasis
+BMGC_DS01664,BMG_DS002086,benign granular cell tumor
+BMGC_DS01665,BMG_DS002087,Myocardial Infarction
+BMGC_DS01666,BMG_DS002088,Myocarditis
+BMGC_DS01667,BMG_DS002089,Interstitial myocarditis
+BMGC_DS01668,BMG_DS002091,myoepithelial tumor
+BMGC_DS01669,BMG_DS002092,Myofascial Pain Syndromes
+BMGC_DS01670,BMG_DS002093,benign muscle neoplasm
+BMGC_DS01671,BMG_DS002094,Myopia
+BMGC_DS01672,BMG_DS002095,muscle cancer
+BMGC_DS01673,BMG_DS002096,Myositis
+BMGC_DS01674,BMG_DS002097,Myositis Ossificans
+BMGC_DS01675,BMG_DS002099,Myotonic Dystrophy
+BMGC_DS01676,BMG_DS002100,Myotonia Congenita
+BMGC_DS01677,BMG_DS002101,Myotonic cataract
+BMGC_DS01678,BMG_DS002103,Myxedema
+BMGC_DS01679,BMG_DS002106,myxosarcoma
+BMGC_DS01680,BMG_DS002109,Nail Diseases
+BMGC_DS01681,BMG_DS002110,Nail-Patella Syndrome
+BMGC_DS01682,BMG_DS002112,narcissistic personality disorder
+BMGC_DS01683,BMG_DS002113,Narcolepsy
+BMGC_DS01684,BMG_DS002114,nasal cavity polyp
+BMGC_DS01685,BMG_DS002116,Nasopharyngeal Diseases
+BMGC_DS01686,BMG_DS002117,nasopharyngeal neoplasm
+BMGC_DS01687,BMG_DS002118,Nasopharyngitis
+BMGC_DS01688,BMG_DS002119,teeth present at birth
+BMGC_DS01689,BMG_DS002120,Necatoriasis
+BMGC_DS01690,BMG_DS002124,Necrobiosis Lipoidica
+BMGC_DS01691,BMG_DS002125,Avascular necrosis of bone
+BMGC_DS01692,BMG_DS002127,Nelson syndrome
+BMGC_DS01693,BMG_DS002129,"Infections, Nematomorpha"
+BMGC_DS01694,BMG_DS002130,Neonatal Abstinence Syndrome
+BMGC_DS01695,BMG_DS002131,Neonatal dacryocystitis and conjunctivitis (disorder)
+BMGC_DS01696,BMG_DS002132,"Congenital, Hereditary, and Neonatal Diseases and Abnormalities"
+BMGC_DS01697,BMG_DS002134,neoplasm
+BMGC_DS01698,BMG_DS002135,embryonal neoplasm
+BMGC_DS01699,BMG_DS002136,connective tissue neoplasm
+BMGC_DS01700,BMG_DS002137,germ cell and embryonal cancer
+BMGC_DS01701,BMG_DS002138,multiple endocrine neoplasia
+BMGC_DS01702,BMG_DS002139,muscle benign neoplasm
+BMGC_DS01703,BMG_DS002140,nervous system cancer
+BMGC_DS01704,BMG_DS002142,hereditary neoplastic syndrome
+BMGC_DS01705,BMG_DS002143,Nephritis
+BMGC_DS01706,BMG_DS002144,Hereditary nephritis
+BMGC_DS01707,BMG_DS002145,"Nephritis, Interstitial"
+BMGC_DS01708,BMG_DS002146,Wilms tumor
+BMGC_DS01709,BMG_DS002147,Nephrocalcinosis
+BMGC_DS01710,BMG_DS002148,Nephrosclerosis
+BMGC_DS01711,BMG_DS002149,Nephrosis
+BMGC_DS01712,BMG_DS002150,Lipoid nephrosis
+BMGC_DS01713,BMG_DS002151,Nephrotic Syndrome
+BMGC_DS01714,BMG_DS002152,nerve compression syndrome
+BMGC_DS01715,BMG_DS002153,neurodegenerative disease
+BMGC_DS01716,BMG_DS002154,nervous system disorder
+BMGC_DS01717,BMG_DS002156,Nesidioblastosis
+BMGC_DS01718,BMG_DS002157,neural tube defect
+BMGC_DS01719,BMG_DS002158,neuralgia
+BMGC_DS01720,BMG_DS002160,schwannoma
+BMGC_DS01721,BMG_DS002161,Neuritis
+BMGC_DS01722,BMG_DS002162,neuroblastoma
+BMGC_DS01723,BMG_DS002163,Neurocirculatory Asthenia
+BMGC_DS01724,BMG_DS002164,Neurodermatitis
+BMGC_DS01725,BMG_DS002165,neurofibroma
+BMGC_DS01726,BMG_DS002166,neurofibromatosis type 1
+BMGC_DS01727,BMG_DS002167,NF2-related schwannomatosis
+BMGC_DS01728,BMG_DS002168,Neuroleptic Malignant Syndrome
+BMGC_DS01729,BMG_DS002169,neuroma
+BMGC_DS01730,BMG_DS002170,acoustic neuroma
+BMGC_DS01731,BMG_DS002171,Neuromuscular Diseases
+BMGC_DS01732,BMG_DS002172,Neuromyelitis Optica
+BMGC_DS01733,BMG_DS002173,Neuronal Ceroid-Lipofuscinoses
+BMGC_DS01734,BMG_DS002174,neuronitis
+BMGC_DS01735,BMG_DS002175,Hereditary Motor and Sensory Neuropathies
+BMGC_DS01736,BMG_DS002176,Hereditary Sensory and Autonomic Neuropathies
+BMGC_DS01737,BMG_DS002177,Neurosyphilis
+BMGC_DS01738,BMG_DS002178,neurotic disorder
+BMGC_DS01739,BMG_DS002179,Neutropenia
+BMGC_DS01740,BMG_DS002181,melanocytic nevus
+BMGC_DS01741,BMG_DS002182,Newcastle Disease
+BMGC_DS01742,BMG_DS002183,nicotine dependence
+BMGC_DS01743,BMG_DS002184,Niemann-Pick Diseases
+BMGC_DS01744,BMG_DS002185,Nyctalopia
+BMGC_DS01745,BMG_DS002186,Nocardia Infections
+BMGC_DS01746,BMG_DS002188,multiple symmetric lipomatosis
+BMGC_DS01747,BMG_DS002190,Noma
+BMGC_DS01748,BMG_DS002193,Noonan Syndrome
+BMGC_DS01749,BMG_DS002194,Crusted scabies
+BMGC_DS01750,BMG_DS002195,Nose Diseases
+BMGC_DS01751,BMG_DS002198,Nocturia
+BMGC_DS01752,BMG_DS002199,Nystagmus
+BMGC_DS01753,BMG_DS002200,Obesity
+BMGC_DS01754,BMG_DS002201,Morbid obesity
+BMGC_DS01755,BMG_DS002202,obsessive-compulsive disorder
+BMGC_DS01756,BMG_DS002203,cerebral artery occlusion
+BMGC_DS01757,BMG_DS002204,"Dermatitis, Occupational"
+BMGC_DS01758,BMG_DS002205,Occupational Diseases
+BMGC_DS01759,BMG_DS002206,Ochronosis
+BMGC_DS01760,BMG_DS002207,Ocular Hypertension
+BMGC_DS01761,BMG_DS002208,Ocular Hypotension
+BMGC_DS01762,BMG_DS002210,Ocular Motility Disorders
+BMGC_DS01763,BMG_DS002211,Ocular Torticollis
+BMGC_DS01764,BMG_DS002212,Oculocerebrorenal Syndrome
+BMGC_DS01765,BMG_DS002213,Oculomotor Nerve Paralysis
+BMGC_DS01766,BMG_DS002217,Oesophagostomiasis
+BMGC_DS01767,BMG_DS002218,oligodendroglioma
+BMGC_DS01768,BMG_DS002219,Oligospermia
+BMGC_DS01769,BMG_DS002220,Oliguria
+BMGC_DS01770,BMG_DS002221,Olivopontocerebellar Atrophies
+BMGC_DS01771,BMG_DS002224,Onchocerciasis
+BMGC_DS01772,BMG_DS002226,Oophoritis
+BMGC_DS01773,BMG_DS002227,ophthalmia neonatorum
+BMGC_DS01774,BMG_DS002228,"Ophthalmia, Sympathetic"
+BMGC_DS01775,BMG_DS002229,ophthalmoplegia
+BMGC_DS01776,BMG_DS002230,opioid abuse
+BMGC_DS01777,BMG_DS002231,Opisthorchiasis
+BMGC_DS01778,BMG_DS002233,Opportunistic mycosis
+BMGC_DS01779,BMG_DS002234,oppositional defiant disorder
+BMGC_DS01780,BMG_DS002235,Optic Atrophy
+BMGC_DS01781,BMG_DS002236,"Optic Atrophies, Hereditary"
+BMGC_DS01782,BMG_DS002237,Optic Disk Drusen
+BMGC_DS01783,BMG_DS002238,Disorder of optic nerve
+BMGC_DS01784,BMG_DS002239,Optic Neuritis
+BMGC_DS01785,BMG_DS002240,oral submucous fibrosis
+BMGC_DS01786,BMG_DS002241,Oral Submucous Fibrosis
+BMGC_DS01787,BMG_DS002242,Orbital Diseases
+BMGC_DS01788,BMG_DS002243,orbit neoplasm
+BMGC_DS01789,BMG_DS002244,Orchitis
+BMGC_DS01790,BMG_DS002245,Organic brain syndrome
+BMGC_DS01791,BMG_DS002246,cognitive disorder
+BMGC_DS01792,BMG_DS002248,Psittacosis
+BMGC_DS01793,BMG_DS002249,Orofaciodigital Syndromes
+BMGC_DS01794,BMG_DS002250,neoplasm of oropharynx
+BMGC_DS01795,BMG_DS002252,Orthomyxoviridae Infections
+BMGC_DS01796,BMG_DS002253,Juvenile osteochondrosis of tibial tubercle
+BMGC_DS01797,BMG_DS002254,Osteitis
+BMGC_DS01798,BMG_DS002255,Osteitis Deformans
+BMGC_DS01799,BMG_DS002256,Osteitis Fibrosa Cystica
+BMGC_DS01800,BMG_DS002257,Degenerative polyarthritis
+BMGC_DS01801,BMG_DS002258,Osteoarthritis of hip
+BMGC_DS01802,BMG_DS002259,"Osteoarthropathy, Primary Hypertrophic"
+BMGC_DS01803,BMG_DS002260,"Osteoarthropathy, Secondary Hypertrophic"
+BMGC_DS01804,BMG_DS002263,Osteochondritis Dissecans
+BMGC_DS01805,BMG_DS002264,Osteochondrodysplasias
+BMGC_DS01806,BMG_DS002266,Osteochondrosis
+BMGC_DS01807,BMG_DS002267,Osteogenesis Imperfecta
+BMGC_DS01808,BMG_DS002268,"Osteolysis, Essential"
+BMGC_DS01809,BMG_DS002270,Massive Osteolyses
+BMGC_DS01810,BMG_DS002273,Osteomalacia
+BMGC_DS01811,BMG_DS002274,Osteomyelitis
+BMGC_DS01812,BMG_DS002275,osteonecrosis
+BMGC_DS01813,BMG_DS002276,Osteopenia
+BMGC_DS01814,BMG_DS002277,Osteopetrosis
+BMGC_DS01815,BMG_DS002278,Osteopoikilosis (disorder)
+BMGC_DS01816,BMG_DS002279,Osteoporosis
+BMGC_DS01817,BMG_DS002280,"Osteoporosis, Postmenopausal"
+BMGC_DS01818,BMG_DS002281,"Osteoporosis, Senile"
+BMGC_DS01819,BMG_DS002283,osteosarcoma
+BMGC_DS01820,BMG_DS002284,Osteosclerosis
+BMGC_DS01821,BMG_DS002285,Ostertagiasis
+BMGC_DS01822,BMG_DS002287,Other acne
+BMGC_DS01823,BMG_DS002288,acute stress disorder
+BMGC_DS01824,BMG_DS002289,pituitary gland disease
+BMGC_DS01825,BMG_DS002291,diversion colitis | chemical colitis
+BMGC_DS01826,BMG_DS002292,ovarian cyst
+BMGC_DS01827,BMG_DS002293,psychotic disorder
+BMGC_DS01828,BMG_DS002298,Other cataract
+BMGC_DS01829,BMG_DS002301,Other chorea
+BMGC_DS01830,BMG_DS002309,Other dermatoses
+BMGC_DS01831,BMG_DS002310,lower respiratory tract disease | upper respiratory tract disease
+BMGC_DS01832,BMG_DS002311,Other respiratory system diseases
+BMGC_DS01833,BMG_DS002312,Other disorders of lens
+BMGC_DS01834,BMG_DS002313,Other disorders of lipoid metabolism
+BMGC_DS01835,BMG_DS002315,plasma protein metabolism disease
+BMGC_DS01836,BMG_DS002316,Other disorders of purine and pyrimidine metabolism
+BMGC_DS01837,BMG_DS002317,Other emphysema
+BMGC_DS01838,BMG_DS002321,heart conduction disease
+BMGC_DS01839,BMG_DS002325,Other impaction of intestine
+BMGC_DS01840,BMG_DS002326,Other inflammatory spondylopathies
+BMGC_DS01841,BMG_DS002328,Other localized visual field defect
+BMGC_DS01842,BMG_DS002332,Other mucopurulent conjunctivitis
+BMGC_DS01843,BMG_DS002337,otosclerosis
+BMGC_DS01844,BMG_DS002338,Other ovarian failure
+BMGC_DS01845,BMG_DS002339,Other peripheral vertigo
+BMGC_DS01846,BMG_DS002340,personality disorder
+BMGC_DS01847,BMG_DS002344,Other specified cardiovascular syphilis
+BMGC_DS01848,BMG_DS002345,urethral stricture
+BMGC_DS01849,BMG_DS002350,Other specified diseases of hard tissues of teeth
+BMGC_DS01850,BMG_DS002351,Other specified diseases of pancreas
+BMGC_DS01851,BMG_DS002353,salivary gland disease
+BMGC_DS01852,BMG_DS002358,Other specified disorders of penis
+BMGC_DS01853,BMG_DS002361,drug dependence
+BMGC_DS01854,BMG_DS002365,pleurisy
+BMGC_DS01855,BMG_DS002366,Other specified gastritis
+BMGC_DS01856,BMG_DS002367,prolapse of female genital organ
+BMGC_DS01857,BMG_DS002370,Other specified hemorrhagic conditions
+BMGC_DS01858,BMG_DS002371,acrodermatitis chronica atrophicans
+BMGC_DS01859,BMG_DS002373,iron deficiency anemia
+BMGC_DS01860,BMG_DS002379,Other specified peritonitis
+BMGC_DS01861,BMG_DS002381,Other specified schistosomiasis
+BMGC_DS01862,BMG_DS002383,Other specified strabismus
+BMGC_DS01863,BMG_DS002384,trigeminal nerve disease
+BMGC_DS01864,BMG_DS002385,Other specified tularemia
+BMGC_DS01865,BMG_DS002386,Other specified urticaria
+BMGC_DS01866,BMG_DS002388,Other specified viral exanthemata
+BMGC_DS01867,BMG_DS002391,Other spontaneous pneumothorax
+BMGC_DS01868,BMG_DS002394,ureteral obstruction
+BMGC_DS01869,BMG_DS002397,Other vitreous opacities
+BMGC_DS01870,BMG_DS002398,Ear Inflammation
+BMGC_DS01871,BMG_DS002399,Otitis Externa
+BMGC_DS01872,BMG_DS002400,Otitis Media
+BMGC_DS01873,BMG_DS002401,Otitis Media with Effusion
+BMGC_DS01874,BMG_DS002402,Suppurative otitis media
+BMGC_DS01875,BMG_DS002403,Otomycosis
+BMGC_DS01876,BMG_DS002406,Ovarian Cysts
+BMGC_DS01877,BMG_DS002407,Ovarian Diseases
+BMGC_DS01878,BMG_DS002409,Oxyuriasis
+BMGC_DS01879,BMG_DS002411,Pachymeningitis
+BMGC_DS01880,BMG_DS002413,extramammary Paget disease
+BMGC_DS01881,BMG_DS002415,Pustulosis of Palms and Soles
+BMGC_DS01882,BMG_DS002417,Pancoast syndrome
+BMGC_DS01883,BMG_DS002418,Pancreatic Cyst
+BMGC_DS01884,BMG_DS002419,Pancreatic Diseases
+BMGC_DS01885,BMG_DS002420,Pancreatic Fistula
+BMGC_DS01886,BMG_DS002421,pancreatic neoplasm
+BMGC_DS01887,BMG_DS002422,Pancreatic Pseudocyst
+BMGC_DS01888,BMG_DS002423,Pancreatitis
+BMGC_DS01889,BMG_DS002424,Pancytopenia
+BMGC_DS01890,BMG_DS002425,panic disorder
+BMGC_DS01891,BMG_DS002426,Panniculitis
+BMGC_DS01892,BMG_DS002428,"Panniculitis, Nodular Nonsuppurative"
+BMGC_DS01893,BMG_DS002430,"Panniculitis, Subacute Nodular Migratory"
+BMGC_DS01894,BMG_DS002431,Panophthalmitis
+BMGC_DS01895,BMG_DS002432,Panuveitis
+BMGC_DS01896,BMG_DS002433,Papilledema
+BMGC_DS01897,BMG_DS002434,papilloma
+BMGC_DS01898,BMG_DS002435,Papillon-Lefevre Disease
+BMGC_DS01899,BMG_DS002437,Phlebotomus Fever
+BMGC_DS01900,BMG_DS002439,Paracoccidioidomycosis
+BMGC_DS01901,BMG_DS002440,paraganglioma
+BMGC_DS01902,BMG_DS002441,Paragonimiasis
+BMGC_DS01903,BMG_DS002442,Parakeratosis
+BMGC_DS01904,BMG_DS002443,Parakeratosis Variegata
+BMGC_DS01905,BMG_DS002444,Progressive bulbar palsy
+BMGC_DS01906,BMG_DS002445,Familial Periodic Paralysis
+BMGC_DS01907,BMG_DS002446,Paralytic Ileus
+BMGC_DS01908,BMG_DS002447,Parametritis
+BMGC_DS01909,BMG_DS002449,paranasal sinus disorder
+BMGC_DS01910,BMG_DS002450,paranasal sinus neoplasm
+BMGC_DS01911,BMG_DS002451,paraneoplastic syndrome
+BMGC_DS01912,BMG_DS002452,paranoid personality disorder
+BMGC_DS01913,BMG_DS002453,Tropical Spastic Paraparesis
+BMGC_DS01914,BMG_DS002455,Paraphimosis
+BMGC_DS01915,BMG_DS002456,Paraplegia
+BMGC_DS01916,BMG_DS002458,Parapsoriasis
+BMGC_DS01917,BMG_DS002459,Parasitic Diseases
+BMGC_DS01918,BMG_DS002460,"Parasitic Diseases, Animal"
+BMGC_DS01919,BMG_DS002461,Parasomnia
+BMGC_DS01920,BMG_DS002462,Parathyroid Diseases
+BMGC_DS01921,BMG_DS002463,tumor of parathyroid gland
+BMGC_DS01922,BMG_DS002464,Paratuberculosis
+BMGC_DS01923,BMG_DS002465,Paratyphoid Fever
+BMGC_DS01924,BMG_DS002466,Paresis
+BMGC_DS01925,BMG_DS002467,Paresthesia
+BMGC_DS01926,BMG_DS002468,Parkinson Disease
+BMGC_DS01927,BMG_DS002469,"Parkinson Disease, Postencephalitic"
+BMGC_DS01928,BMG_DS002470,Secondary Parkinson Disease
+BMGC_DS01929,BMG_DS002471,Paronychia (disorder)
+BMGC_DS01930,BMG_DS002472,Parotid Diseases
+BMGC_DS01931,BMG_DS002474,Parotitis
+BMGC_DS01932,BMG_DS002475,Parovarian Cyst
+BMGC_DS01933,BMG_DS002476,Paroxysmal atrial tachycardia
+BMGC_DS01934,BMG_DS002477,Paroxysmal supraventricular tachycardia
+BMGC_DS01935,BMG_DS002479,Pars Planitis
+BMGC_DS01936,BMG_DS002481,"Passive Addiction, Neonatal"
+BMGC_DS01937,BMG_DS002482,Pasteurella Infections
+BMGC_DS01938,BMG_DS002483,pathological gambling
+BMGC_DS01939,BMG_DS002484,Lice Infestations
+BMGC_DS01940,BMG_DS002485,Pediculus capitis infestation
+BMGC_DS01941,BMG_DS002486,Body louse infestation
+BMGC_DS01942,BMG_DS002487,Infestation by Phthirus pubis
+BMGC_DS01943,BMG_DS002489,Pelger-Huet Anomaly
+BMGC_DS01944,BMG_DS002490,Peliosis Hepatis
+BMGC_DS01945,BMG_DS002491,Pellagra
+BMGC_DS01946,BMG_DS002492,Pelvic abscess
+BMGC_DS01947,BMG_DS002493,Pelvic Infection
+BMGC_DS01948,BMG_DS002494,"Pemphigoid, Benign Mucous Membrane"
+BMGC_DS01949,BMG_DS002495,Bullous pemphigoid
+BMGC_DS01950,BMG_DS002496,Pemphigus
+BMGC_DS01951,BMG_DS002497,Pemphigus Vulgaris
+BMGC_DS01952,BMG_DS002499,Penile Diseases
+BMGC_DS01953,BMG_DS002500,Peyronie Disease
+BMGC_DS01954,BMG_DS002501,penile neoplasm
+BMGC_DS01955,BMG_DS002502,Peptic Ulcer
+BMGC_DS01956,BMG_DS002503,Peptic Ulcer Perforation
+BMGC_DS01957,BMG_DS002506,Suppurative Periapical Periodontitis
+BMGC_DS01958,BMG_DS002508,Periapical Granuloma
+BMGC_DS01959,BMG_DS002509,Periapical Periodontitis
+BMGC_DS01960,BMG_DS002512,Polyarteritis Nodosa
+BMGC_DS01961,BMG_DS002513,Periarthritis
+BMGC_DS01962,BMG_DS002514,Pericardial effusion
+BMGC_DS01963,BMG_DS002515,Pericarditis
+BMGC_DS01964,BMG_DS002516,"Pericarditis, Constrictive"
+BMGC_DS01965,BMG_DS002518,Pericementitis
+BMGC_DS01966,BMG_DS002519,Pericholangitis
+BMGC_DS01967,BMG_DS002521,Pericoronitis
+BMGC_DS01968,BMG_DS002522,Perinephritis
+BMGC_DS01969,BMG_DS002523,Familial Mediterranean Fever
+BMGC_DS01970,BMG_DS002525,Periodontal Diseases
+BMGC_DS01971,BMG_DS002526,Periodontitis
+BMGC_DS01972,BMG_DS002527,Aggressive Periodontitis
+BMGC_DS01973,BMG_DS002528,Periostitis
+BMGC_DS01974,BMG_DS002529,peripheral vascular disease
+BMGC_DS01975,BMG_DS002530,peripheral neuropathy
+BMGC_DS01976,BMG_DS002531,peripheral nervous system neoplasm
+BMGC_DS01977,BMG_DS002534,Periphlebitis
+BMGC_DS01978,BMG_DS002537,peritoneal neoplasm
+BMGC_DS01979,BMG_DS002538,peritonitis
+BMGC_DS01980,BMG_DS002539,Peritonsillar Abscess
+BMGC_DS01981,BMG_DS002542,Persistent Fetal Circulation Syndrome
+BMGC_DS01982,BMG_DS002545,Peutz-Jeghers Syndrome
+BMGC_DS01983,BMG_DS002546,Phagocyte Bactericidal Dysfunction
+BMGC_DS01984,BMG_DS002547,Pharyngeal Diseases
+BMGC_DS01985,BMG_DS002548,pharynx neoplasm
+BMGC_DS01986,BMG_DS002549,Pharyngitis
+BMGC_DS01987,BMG_DS002550,Pharyngo-Conjunctival Fever
+BMGC_DS01988,BMG_DS002551,phencyclidine abuse
+BMGC_DS01989,BMG_DS002552,Phenylketonurias
+BMGC_DS01990,BMG_DS002553,pheochromocytoma
+BMGC_DS01991,BMG_DS002554,phimosis
+BMGC_DS01992,BMG_DS002555,phlebitis
+BMGC_DS01993,BMG_DS002556,Phlegmasia Alba Dolens
+BMGC_DS01994,BMG_DS002557,social phobia
+BMGC_DS01995,BMG_DS002558,Phosphorus Metabolism Disorders
+BMGC_DS01996,BMG_DS002559,Polymorphous light eruption
+BMGC_DS01997,BMG_DS002560,Photosensitivity Disorders
+BMGC_DS01998,BMG_DS002562,pica disease
+BMGC_DS01999,BMG_DS002563,Pick Disease of Heart
+BMGC_DS02000,BMG_DS002564,Obesity Hypoventilation Syndrome
+BMGC_DS02001,BMG_DS002566,Piedra
+BMGC_DS02002,BMG_DS002567,isolated Pierre-Robin syndrome
+BMGC_DS02003,BMG_DS002569,pilonidal sinus
+BMGC_DS02004,BMG_DS002570,pineal gland cancer
+BMGC_DS02005,BMG_DS002571,Pinta
+BMGC_DS02006,BMG_DS002572,pituitary gland adenoma
+BMGC_DS02007,BMG_DS002573,Pituitary Apoplexy
+BMGC_DS02008,BMG_DS002574,Pituitary Diseases
+BMGC_DS02009,BMG_DS002575,pituitary tumor
+BMGC_DS02010,BMG_DS002576,Pityriasis
+BMGC_DS02011,BMG_DS002577,Pityriasis Rosea
+BMGC_DS02012,BMG_DS002578,Pityriasis Rubra Pilaris
+BMGC_DS02013,BMG_DS002579,placenta accreta
+BMGC_DS02014,BMG_DS002580,placenta disorder
+BMGC_DS02015,BMG_DS002581,placenta praevia
+BMGC_DS02016,BMG_DS002582,Placental Insufficiency
+BMGC_DS02017,BMG_DS002584,Plague
+BMGC_DS02018,BMG_DS002587,plasmacytoma
+BMGC_DS02019,BMG_DS002588,Platelet Storage Pool Deficiency
+BMGC_DS02020,BMG_DS002589,Pleural Diseases
+BMGC_DS02021,BMG_DS002590,pleural neoplasm
+BMGC_DS02022,BMG_DS002591,Pleurisy
+BMGC_DS02023,BMG_DS002592,"Pleurodynia, Epidemic"
+BMGC_DS02024,BMG_DS002593,Pleuropneumonia
+BMGC_DS02025,BMG_DS002596,Pneumatosis Cystoides Intestinalis
+BMGC_DS02026,BMG_DS002598,Pneumococcal Infections
+BMGC_DS02027,BMG_DS002599,Pneumoconiosis
+BMGC_DS02028,BMG_DS002601,Pneumonia
+BMGC_DS02029,BMG_DS002603,Aspiration Pneumonia
+BMGC_DS02030,BMG_DS002605,"Pneumonia, Lipid"
+BMGC_DS02031,BMG_DS002606,Lobar Pneumonia
+BMGC_DS02032,BMG_DS002607,Mycoplasma pneumonia
+BMGC_DS02033,BMG_DS002610,Staphylococcal Pneumonia
+BMGC_DS02034,BMG_DS002611,"Pneumonia, Viral"
+BMGC_DS02035,BMG_DS002612,Pneumopericardium
+BMGC_DS02036,BMG_DS002614,Pneumothorax
+BMGC_DS02037,BMG_DS002615,Rothmund-Thomson syndrome
+BMGC_DS02038,BMG_DS002616,"Dermatitis, Toxicodendron"
+BMGC_DS02039,BMG_DS002617,Poland Syndrome
+BMGC_DS02040,BMG_DS002618,Poliomyelitis
+BMGC_DS02041,BMG_DS002620,"Polychondritis, Relapsing"
+BMGC_DS02042,BMG_DS002621,Polycystic Ovary Syndrome
+BMGC_DS02043,BMG_DS002622,Polycythemia
+BMGC_DS02044,BMG_DS002623,acquired polycythemia vera
+BMGC_DS02045,BMG_DS002624,Polymenorrhea
+BMGC_DS02046,BMG_DS002625,Polymyalgia Rheumatica
+BMGC_DS02047,BMG_DS002626,Polyneuritis
+BMGC_DS02048,BMG_DS002628,polyploidy
+BMGC_DS02049,BMG_DS002629,classic familial adenomatous polyposis
+BMGC_DS02050,BMG_DS002630,polyp
+BMGC_DS02051,BMG_DS002631,Polyradiculopathy
+BMGC_DS02052,BMG_DS002632,Polyradiculoneuropathy
+BMGC_DS02053,BMG_DS002633,Vesicular eczema of hands and/or feet
+BMGC_DS02054,BMG_DS002634,popliteal cyst
+BMGC_DS02055,BMG_DS002636,porphyrin metabolism disease
+BMGC_DS02056,BMG_DS002639,Postgastrectomy Syndromes
+BMGC_DS02057,BMG_DS002640,Postherpetic neuralgia
+BMGC_DS02058,BMG_DS002643,Postphlebitic Syndrome
+BMGC_DS02059,BMG_DS002649,Prader-Willi Syndrome
+BMGC_DS02060,BMG_DS002650,preeclampsia
+BMGC_DS02061,BMG_DS002654,placenta disease
+BMGC_DS02062,BMG_DS002655,"Pregnancy Complications, Cardiovascular"
+BMGC_DS02063,BMG_DS002656,"Pregnancy Complications, Hematologic"
+BMGC_DS02064,BMG_DS002657,"Pregnancy Complications, Infectious"
+BMGC_DS02065,BMG_DS002660,ectopic pregnancy
+BMGC_DS02066,BMG_DS002663,Atrial Premature Complexes
+BMGC_DS02067,BMG_DS002664,premature ejaculation
+BMGC_DS02068,BMG_DS002667,Presbyopia
+BMGC_DS02069,BMG_DS002669,Priapism
+BMGC_DS02070,BMG_DS002671,"Cerebellar Degenerations, Primary"
+BMGC_DS02071,BMG_DS002672,Primary Insomnia
+BMGC_DS02072,BMG_DS002673,"Cardiomyopathies, Primary"
+BMGC_DS02073,BMG_DS002674,Proctitis
+BMGC_DS02074,BMG_DS002678,Progeria
+BMGC_DS02075,BMG_DS002680,prolactin-producing pituitary gland adenoma
+BMGC_DS02076,BMG_DS002682,Prostatic Diseases
+BMGC_DS02077,BMG_DS002683,prostate neoplasm
+BMGC_DS02078,BMG_DS002685,prostatitis
+BMGC_DS02079,BMG_DS002686,Prosthesis Loosening
+BMGC_DS02080,BMG_DS002687,Protein Deficiency
+BMGC_DS02081,BMG_DS002688,protein-energy malnutrition
+BMGC_DS02082,BMG_DS002689,Protein-Losing Enteropathies
+BMGC_DS02083,BMG_DS002690,proteinuria
+BMGC_DS02084,BMG_DS002691,Proteus Infections
+BMGC_DS02085,BMG_DS002693,Protozoan Infections
+BMGC_DS02086,BMG_DS002695,Prune Belly Syndrome
+BMGC_DS02087,BMG_DS002698,Pseudo-Hurler Polydystrophy
+BMGC_DS02088,BMG_DS002699,Pseudobulbar Palsy
+BMGC_DS02089,BMG_DS002701,Pseudogout
+BMGC_DS02090,BMG_DS002702,pseudohermaphroditism
+BMGC_DS02091,BMG_DS002703,Pseudohypoaldosteronism
+BMGC_DS02092,BMG_DS002704,Pseudohypoparathyroidism
+BMGC_DS02093,BMG_DS002705,Pseudomonas Infections
+BMGC_DS02094,BMG_DS002706,pseudomyxoma peritonei
+BMGC_DS02095,BMG_DS002707,Pseudopseudohypoparathyroidism
+BMGC_DS02096,BMG_DS002708,Kimura Disease
+BMGC_DS02097,BMG_DS002710,Pseudotumor Cerebri
+BMGC_DS02098,BMG_DS002711,Pseudoxanthoma Elasticum
+BMGC_DS02099,BMG_DS002712,Psoriasis
+BMGC_DS02100,BMG_DS002713,Tension Headache
+BMGC_DS02101,BMG_DS002714,alcoholic psychosis
+BMGC_DS02102,BMG_DS002715,drug psychosis
+BMGC_DS02103,BMG_DS002717,inhibited female orgasm
+BMGC_DS02104,BMG_DS002718,male orgasm disorder
+BMGC_DS02105,BMG_DS002719,psychosexual disorder
+BMGC_DS02106,BMG_DS002721,psychotic disorder
+BMGC_DS02107,BMG_DS002722,pterygium
+BMGC_DS02108,BMG_DS002723,Precocious Puberty
+BMGC_DS02109,BMG_DS002724,Puerperal Disorders
+BMGC_DS02110,BMG_DS002725,Puerperal Infection
+BMGC_DS02111,BMG_DS002727,Pulmonary Alveolar Proteinosis
+BMGC_DS02112,BMG_DS002728,pulmonary edema
+BMGC_DS02113,BMG_DS002729,pulmonary embolism
+BMGC_DS02114,BMG_DS002730,Pulmonary embolism with pulmonary infarction
+BMGC_DS02115,BMG_DS002731,Pulmonary Emphysema
+BMGC_DS02116,BMG_DS002732,Pulmonary Eosinophilia
+BMGC_DS02117,BMG_DS002733,Pulmonary Fibrosis
+BMGC_DS02118,BMG_DS002734,Cor pulmonale
+BMGC_DS02119,BMG_DS002735,Pulmonary Infarction
+BMGC_DS02120,BMG_DS002736,pulmonary subvalvular stenosis
+BMGC_DS02121,BMG_DS002737,pulmonary valve disorder
+BMGC_DS02122,BMG_DS002738,pulmonary valve insufficiency
+BMGC_DS02123,BMG_DS002739,Pulmonary Valve Stenosis
+BMGC_DS02124,BMG_DS002740,pulmonary venoocclusive disease
+BMGC_DS02125,BMG_DS002741,Pulp degeneration
+BMGC_DS02126,BMG_DS002742,Pulpitis
+BMGC_DS02127,BMG_DS002743,Pupil Disorders
+BMGC_DS02128,BMG_DS002744,"Purine-Pyrimidine Metabolism, Inborn Errors"
+BMGC_DS02129,BMG_DS002745,Purpura
+BMGC_DS02130,BMG_DS002746,"Purpura, Hyperglobulinemic"
+BMGC_DS02131,BMG_DS002747,Henoch-Schoenlein Purpura
+BMGC_DS02132,BMG_DS002748,"Purpura, Thrombotic Thrombocytopenic"
+BMGC_DS02133,BMG_DS002749,Pyelitis
+BMGC_DS02134,BMG_DS002751,Pyelonephritis
+BMGC_DS02135,BMG_DS002752,"Pyelonephritis, Xanthogranulomatous"
+BMGC_DS02136,BMG_DS002754,pyloric stenosis
+BMGC_DS02137,BMG_DS002755,Pyoderma
+BMGC_DS02138,BMG_DS002759,Pyosalpinx
+BMGC_DS02139,BMG_DS002760,Pyoureter
+BMGC_DS02140,BMG_DS002761,Pyruvate Carboxylase Deficiency Disease
+BMGC_DS02141,BMG_DS002762,Pyruvate Dehydrogenase Complex Deficiency Disease
+BMGC_DS02142,BMG_DS002763,"Pyruvate Metabolism, Inborn Errors"
+BMGC_DS02143,BMG_DS002764,pyuria
+BMGC_DS02144,BMG_DS002765,Q Fever
+BMGC_DS02145,BMG_DS002766,Quadriplegia
+BMGC_DS02146,BMG_DS002767,Rabies (disorder)
+BMGC_DS02147,BMG_DS002768,Radiation Syndrome
+BMGC_DS02148,BMG_DS002769,Radiculitis
+BMGC_DS02149,BMG_DS002770,Radiation-Induced Dermatitis
+BMGC_DS02150,BMG_DS002772,Rat-Bite Fever
+BMGC_DS02151,BMG_DS002773,Raynaud Disease
+BMGC_DS02152,BMG_DS002774,Raynaud Phenomenon
+BMGC_DS02153,BMG_DS002776,Rectal Diseases
+BMGC_DS02154,BMG_DS002777,rectal neoplasm
+BMGC_DS02155,BMG_DS002779,Rectal Prolapse
+BMGC_DS02156,BMG_DS002780,Pure Red-Cell Aplasia
+BMGC_DS02157,BMG_DS002782,Reflex Sympathetic Dystrophy
+BMGC_DS02158,BMG_DS002783,Refractive Errors
+BMGC_DS02159,BMG_DS002784,Refsum Disease
+BMGC_DS02160,BMG_DS002785,Reiter Syndrome
+BMGC_DS02161,BMG_DS002786,Relapsing Fever
+BMGC_DS02162,BMG_DS002787,Tick-borne relapsing fever
+BMGC_DS02163,BMG_DS002788,Renal Artery Obstruction
+BMGC_DS02164,BMG_DS002789,Renal Artery Stenosis
+BMGC_DS02165,BMG_DS002790,Kidney Failure
+BMGC_DS02166,BMG_DS002792,Renal Osteodystrophy
+BMGC_DS02167,BMG_DS002793,"Renal Tubular Transport, Inborn Errors"
+BMGC_DS02168,BMG_DS002796,Respiration Disorders
+BMGC_DS02169,BMG_DS002797,"Respiratory Distress Syndrome, Newborn"
+BMGC_DS02170,BMG_DS002798,"Respiratory Distress Syndrome, Adult"
+BMGC_DS02171,BMG_DS002800,Respiratory Syncytial Virus Infections
+BMGC_DS02172,BMG_DS002801,Respiratory Tract Diseases
+BMGC_DS02173,BMG_DS002802,Respiratory Tract Infections
+BMGC_DS02174,BMG_DS002804,Restless Legs Syndrome
+BMGC_DS02175,BMG_DS002806,"reticuloendotheliosis, X-linked"
+BMGC_DS02176,BMG_DS002807,reticulohistiocytic granuloma
+BMGC_DS02177,BMG_DS002808,Retinal Artery Occlusion
+BMGC_DS02178,BMG_DS002809,retinal degeneration
+BMGC_DS02179,BMG_DS002810,Retinal Detachment
+BMGC_DS02180,BMG_DS002811,Retinal Diseases
+BMGC_DS02181,BMG_DS002812,Retinal Drusen
+BMGC_DS02182,BMG_DS002813,"Retinal Necrosis Syndrome, Acute"
+BMGC_DS02183,BMG_DS002814,Retinal Perforations
+BMGC_DS02184,BMG_DS002815,Retinal vascular occlusion
+BMGC_DS02185,BMG_DS002816,Retinal Vein Occlusion
+BMGC_DS02186,BMG_DS002817,Retinitis
+BMGC_DS02187,BMG_DS002818,Retinitis Pigmentosa
+BMGC_DS02188,BMG_DS002819,retinoblastoma
+BMGC_DS02189,BMG_DS002820,Retinopathy of Prematurity
+BMGC_DS02190,BMG_DS002821,Retrocochlear Diseases
+BMGC_DS02191,BMG_DS002822,Retroperitoneal fibrosis
+BMGC_DS02192,BMG_DS002823,retroperitoneal neoplasm
+BMGC_DS02193,BMG_DS002825,Rett Syndrome
+BMGC_DS02194,BMG_DS002826,Reye Syndrome
+BMGC_DS02195,BMG_DS002827,Rh Isoimmunization
+BMGC_DS02196,BMG_DS002829,rhabdomyosarcoma
+BMGC_DS02197,BMG_DS002830,Rheumatism
+BMGC_DS02198,BMG_DS002831,Rheumatic Fever
+BMGC_DS02199,BMG_DS002832,Rheumatic Heart Disease
+BMGC_DS02200,BMG_DS002833,Acute rheumatic heart disease
+BMGC_DS02201,BMG_DS002836,Rhinitis
+BMGC_DS02202,BMG_DS002837,"Rhinitis, Allergic, Perennial"
+BMGC_DS02203,BMG_DS002838,"Rhinitis, Atrophic"
+BMGC_DS02204,BMG_DS002839,"Rhinitis, Vasomotor"
+BMGC_DS02205,BMG_DS002841,Rhinoscleroma
+BMGC_DS02206,BMG_DS002843,Riboflavin Deficiency
+BMGC_DS02207,BMG_DS002844,Rickets
+BMGC_DS02208,BMG_DS002845,Rickettsia Infections
+BMGC_DS02209,BMG_DS002847,Rickettsialpox
+BMGC_DS02210,BMG_DS002848,Rift Valley Fever
+BMGC_DS02211,BMG_DS002849,right aortic arch
+BMGC_DS02212,BMG_DS002852,ring chromosome syndrome
+BMGC_DS02213,BMG_DS002854,Rocky Mountain Spotted Fever
+BMGC_DS02214,BMG_DS002855,Rodent Diseases
+BMGC_DS02215,BMG_DS002856,Root Resorption
+BMGC_DS02216,BMG_DS002857,Rosacea
+BMGC_DS02217,BMG_DS002858,Rotavirus Infections
+BMGC_DS02218,BMG_DS002859,Rubella
+BMGC_DS02219,BMG_DS002861,Rubinstein-Taybi Syndrome
+BMGC_DS02220,BMG_DS002862,Saldino-Noonan Syndrome
+BMGC_DS02221,BMG_DS002864,Sialolithiasis
+BMGC_DS02222,BMG_DS002865,Salivary Gland Diseases
+BMGC_DS02223,BMG_DS002866,tumor of salivary gland
+BMGC_DS02224,BMG_DS002867,Salmonella food poisoning
+BMGC_DS02225,BMG_DS002868,salmonellosis
+BMGC_DS02226,BMG_DS002869,"Salmonella Infections, Animal"
+BMGC_DS02227,BMG_DS002870,Salpingitis
+BMGC_DS02228,BMG_DS002871,Tubo-ovarian inflammatory disease
+BMGC_DS02229,BMG_DS002872,Sandhoff Disease
+BMGC_DS02230,BMG_DS002873,Sarcoidosis
+BMGC_DS02231,BMG_DS002874,Cutaneous sarcoidosis
+BMGC_DS02232,BMG_DS002876,"Sarcoidosis, Pulmonary"
+BMGC_DS02233,BMG_DS002880,Kaposi's sarcoma
+BMGC_DS02234,BMG_DS002881,mast cell sarcoma
+BMGC_DS02235,BMG_DS002882,Sarcocystosis
+BMGC_DS02236,BMG_DS002883,scabies
+BMGC_DS02237,BMG_DS002884,Scalp Dermatoses
+BMGC_DS02238,BMG_DS002886,Scarlet Fever
+BMGC_DS02239,BMG_DS002887,Schamberg Disease
+BMGC_DS02240,BMG_DS002888,Scheuermann's Disease
+BMGC_DS02241,BMG_DS002889,Schistosomiasis
+BMGC_DS02242,BMG_DS002890,Schistosomiasis japonica
+BMGC_DS02243,BMG_DS002891,Schistosomiasis mansoni
+BMGC_DS02244,BMG_DS002894,schizoaffective disorder
+BMGC_DS02245,BMG_DS002895,schizoid personality disorder
+BMGC_DS02246,BMG_DS002896,schizophrenia
+BMGC_DS02247,BMG_DS002897,childhood-onset schizophrenia
+BMGC_DS02248,BMG_DS002898,paranoid schizophrenia
+BMGC_DS02249,BMG_DS002899,schizophreniform disorder
+BMGC_DS02250,BMG_DS002900,schizotypal personality disorder
+BMGC_DS02251,BMG_DS002901,Schwartz-Jampel Syndrome
+BMGC_DS02252,BMG_DS002903,Scimitar Syndrome
+BMGC_DS02253,BMG_DS002904,Scleral Diseases
+BMGC_DS02254,BMG_DS002905,Scleredema Adultorum
+BMGC_DS02255,BMG_DS002907,Scleritis
+BMGC_DS02256,BMG_DS002908,Localized scleroderma
+BMGC_DS02257,BMG_DS002909,Systemic Scleroderma
+BMGC_DS02258,BMG_DS002910,"Scoliosis, unspecified"
+BMGC_DS02259,BMG_DS002911,scotoma
+BMGC_DS02260,BMG_DS002912,Scrapie
+BMGC_DS02261,BMG_DS002913,Screw Worm Infection
+BMGC_DS02262,BMG_DS002915,Scrub Typhus
+BMGC_DS02263,BMG_DS002916,Scurvy
+BMGC_DS02264,BMG_DS002917,Sea-Blue Histiocyte Syndrome
+BMGC_DS02265,BMG_DS002918,Seasickness
+BMGC_DS02266,BMG_DS002919,Sebaceous Gland Diseases
+BMGC_DS02267,BMG_DS002920,sebaceous gland neoplasm
+BMGC_DS02268,BMG_DS002921,Seborrheic dermatitis
+BMGC_DS02269,BMG_DS002922,"Myocardial Diseases, Secondary"
+BMGC_DS02270,BMG_DS002923,seminoma
+BMGC_DS02271,BMG_DS002924,senile cataract
+BMGC_DS02272,BMG_DS002926,Sensation Disorders
+BMGC_DS02273,BMG_DS002930,Septicemia
+BMGC_DS02274,BMG_DS002932,Sertoli cell tumor
+BMGC_DS02275,BMG_DS002933,Serum Sickness
+BMGC_DS02276,BMG_DS002934,Setariasis
+BMGC_DS02277,BMG_DS002935,Sex Chromosome Aberrations
+BMGC_DS02278,BMG_DS002936,disorder of sexual development
+BMGC_DS02279,BMG_DS002942,Sezary syndrome
+BMGC_DS02280,BMG_DS002945,cardiogenic shock
+BMGC_DS02281,BMG_DS002946,Short Bowel Syndrome
+BMGC_DS02282,BMG_DS002947,Short Rib-Polydactyly Syndrome
+BMGC_DS02283,BMG_DS002948,Shwartzman Phenomenon
+BMGC_DS02284,BMG_DS002949,Shy-Drager Syndrome
+BMGC_DS02285,BMG_DS002950,Sialadenitis
+BMGC_DS02286,BMG_DS002951,"Sialometaplasia, Necrotizing"
+BMGC_DS02287,BMG_DS002952,Sialorrhea
+BMGC_DS02288,BMG_DS002953,Sick Building Syndrome
+BMGC_DS02289,BMG_DS002954,Sick Sinus Syndrome
+BMGC_DS02290,BMG_DS002955,Sickle Cell Trait
+BMGC_DS02291,BMG_DS002956,Siderosis
+BMGC_DS02292,BMG_DS002957,Sigmoid Diseases
+BMGC_DS02293,BMG_DS002958,sigmoid neoplasm
+BMGC_DS02294,BMG_DS002960,Silicosis
+BMGC_DS02295,BMG_DS002962,Silo Filler's Disease
+BMGC_DS02296,BMG_DS002963,B Virus Infection
+BMGC_DS02297,BMG_DS002965,Single-Gene Defects
+BMGC_DS02298,BMG_DS002966,Sinoatrial Block
+BMGC_DS02299,BMG_DS002967,"Sinus Thrombosis, Intracranial"
+BMGC_DS02300,BMG_DS002968,Sinusitis
+BMGC_DS02301,BMG_DS002969,sirenomelia
+BMGC_DS02302,BMG_DS002970,situs inversus
+BMGC_DS02303,BMG_DS002971,Sjogren-Larsson Syndrome
+BMGC_DS02304,BMG_DS002973,skin disorder
+BMGC_DS02305,BMG_DS002974,"Skin Diseases, Vesiculobullous"
+BMGC_DS02306,BMG_DS002975,"Skin Diseases, Genetic"
+BMGC_DS02307,BMG_DS002976,"Skin Diseases, Infectious"
+BMGC_DS02308,BMG_DS002980,skin neoplasm
+BMGC_DS02309,BMG_DS002981,skin tag
+BMGC_DS02310,BMG_DS002982,Skin Ulcer
+BMGC_DS02311,BMG_DS002983,skull neoplasm
+BMGC_DS02312,BMG_DS002984,Sleep Apnea Syndromes
+BMGC_DS02313,BMG_DS002986,Smallpox
+BMGC_DS02314,BMG_DS002990,soft tissue neoplasm
+BMGC_DS02315,BMG_DS002992,solitary cyst of breast
+BMGC_DS02316,BMG_DS002993,somatoform disorder
+BMGC_DS02317,BMG_DS002994,somatostatinoma
+BMGC_DS02318,BMG_DS002995,Somnambulism
+BMGC_DS02319,BMG_DS002996,Sparganosis
+BMGC_DS02320,BMG_DS002997,Spasmophilia
+BMGC_DS02321,BMG_DS002998,West Syndrome
+BMGC_DS02322,BMG_DS002999,Spastic Paraplegia
+BMGC_DS02323,BMG_DS003000,"Spastic Paraplegia, Hereditary"
+BMGC_DS02324,BMG_DS003002,Speech Disorders
+BMGC_DS02325,BMG_DS003003,Spermatic Cord Torsion
+BMGC_DS02326,BMG_DS003004,Spermatocele
+BMGC_DS02327,BMG_DS003005,Sphenoid Sinusitis
+BMGC_DS02328,BMG_DS003007,Hereditary spherocytosis
+BMGC_DS02329,BMG_DS003008,Sphingolipidoses
+BMGC_DS02330,BMG_DS003009,spina bifida cystica
+BMGC_DS02331,BMG_DS003011,Compression of spinal cord
+BMGC_DS02332,BMG_DS003012,Spinal Cord Diseases
+BMGC_DS02333,BMG_DS003013,spinal cord neoplasm
+BMGC_DS02334,BMG_DS003014,Spinal Diseases
+BMGC_DS02335,BMG_DS003015,spinal cancer
+BMGC_DS02336,BMG_DS003018,Spinocerebellar Degeneration
+BMGC_DS02337,BMG_DS003020,Splenic Diseases
+BMGC_DS02338,BMG_DS003021,Splenic Infarction
+BMGC_DS02339,BMG_DS003022,spleen neoplasm
+BMGC_DS02340,BMG_DS003023,Spondylitis
+BMGC_DS02341,BMG_DS003024,Ankylosing spondylitis
+BMGC_DS02342,BMG_DS003025,Spondyloepiphyseal Dysplasia
+BMGC_DS02343,BMG_DS003026,Spondylolisthesis
+BMGC_DS02344,BMG_DS003027,Spondylolysis
+BMGC_DS02345,BMG_DS003028,Spondylosis
+BMGC_DS02346,BMG_DS003029,Spondylosis Deformans
+BMGC_DS02347,BMG_DS003031,Spotted Fever Group Rickettsiosis
+BMGC_DS02348,BMG_DS003032,"Sprue, Tropical"
+BMGC_DS02349,BMG_DS003033,stutter disorder
+BMGC_DS02350,BMG_DS003034,Staphylococcal enterocolitis
+BMGC_DS02351,BMG_DS003036,Staphylococcal Infections
+BMGC_DS02352,BMG_DS003038,Staphylococcal Skin Infections
+BMGC_DS02353,BMG_DS003039,Status Asthmaticus
+BMGC_DS02354,BMG_DS003040,Status Epilepticus
+BMGC_DS02355,BMG_DS003042,steatorrhea
+BMGC_DS02356,BMG_DS003044,stereotypic movement disorder
+BMGC_DS02357,BMG_DS003045,Stevens-Johnson Syndrome
+BMGC_DS02358,BMG_DS003046,Gastric Dilatation
+BMGC_DS02359,BMG_DS003047,Stomach Diseases
+BMGC_DS02360,BMG_DS003048,gastric neoplasm
+BMGC_DS02361,BMG_DS003050,Gastric ulcer
+BMGC_DS02362,BMG_DS003052,Stomatitis
+BMGC_DS02363,BMG_DS003053,Aphthous Stomatitis
+BMGC_DS02364,BMG_DS003054,"Stomatitis, Denture"
+BMGC_DS02365,BMG_DS003056,Ulcerative stomatitis
+BMGC_DS02366,BMG_DS003057,Stomatognathic Diseases
+BMGC_DS02367,BMG_DS003058,Strabismus
+BMGC_DS02368,BMG_DS003059,Streptococcal Infections
+BMGC_DS02369,BMG_DS003060,post-traumatic stress disorder
+BMGC_DS02370,BMG_DS003061,Female stress incontinence
+BMGC_DS02371,BMG_DS003062,Cerebrovascular accident
+BMGC_DS02372,BMG_DS003063,"Stromal Dystrophies, Corneal"
+BMGC_DS02373,BMG_DS003064,"Strongyle Infections, Equine"
+BMGC_DS02374,BMG_DS003065,Strongyloidiasis
+BMGC_DS02375,BMG_DS003067,Sturge-Weber Syndrome
+BMGC_DS02376,BMG_DS003068,stuttering
+BMGC_DS02377,BMG_DS003069,Subacute Sclerosing Panencephalitis
+BMGC_DS02378,BMG_DS003070,Subarachnoid Hemorrhage
+BMGC_DS02379,BMG_DS003071,Subclavian Steal Syndrome
+BMGC_DS02380,BMG_DS003072,"Empyema, Subdural"
+BMGC_DS02381,BMG_DS003074,Submandibular Gland Diseases
+BMGC_DS02382,BMG_DS003081,Sudden infant death syndrome
+BMGC_DS02383,BMG_DS003082,Sulfhemoglobinemia
+BMGC_DS02384,BMG_DS003084,Superinfection
+BMGC_DS02385,BMG_DS003085,Superior Mesenteric Artery Syndrome
+BMGC_DS02386,BMG_DS003086,Superior Vena Cava Syndrome
+BMGC_DS02387,BMG_DS003087,Superior Vena Cava Thrombosis
+BMGC_DS02388,BMG_DS003088,Progressive supranuclear palsy
+BMGC_DS02389,BMG_DS003089,"Neuralgia, Supraorbital"
+BMGC_DS02390,BMG_DS003090,supratentorial cancer
+BMGC_DS02391,BMG_DS003091,copper deficiency myelopathy
+BMGC_DS02392,BMG_DS003092,Sweat Gland Diseases
+BMGC_DS02393,BMG_DS003093,sweat gland neoplasm
+BMGC_DS02394,BMG_DS003095,"Sweating, Gustatory"
+BMGC_DS02395,BMG_DS003096,Swine Diseases
+BMGC_DS02396,BMG_DS003099,Sycosis
+BMGC_DS02397,BMG_DS003100,syndactyly
+BMGC_DS02398,BMG_DS003101,Syndrome
+BMGC_DS02399,BMG_DS003103,synostosis
+BMGC_DS02400,BMG_DS003104,synovial sarcoma
+BMGC_DS02401,BMG_DS003105,Synovitis
+BMGC_DS02402,BMG_DS003107,"tenosynovial giant cell tumor, diffuse type"
+BMGC_DS02403,BMG_DS003109,Syphilis
+BMGC_DS02404,BMG_DS003111,"Syphilis, Congenital"
+BMGC_DS02405,BMG_DS003113,"Syphilis, Latent"
+BMGC_DS02406,BMG_DS003115,Syringomyelia
+BMGC_DS02407,BMG_DS003117,Tabes Dorsalis
+BMGC_DS02408,BMG_DS003118,"Tachycardia, Atrioventricular Nodal Reentry"
+BMGC_DS02409,BMG_DS003119,"Tachycardia, Ectopic Atrial"
+BMGC_DS02410,BMG_DS003121,"Tachycardia, Paroxysmal"
+BMGC_DS02411,BMG_DS003123,Sinus Tachycardia
+BMGC_DS02412,BMG_DS003124,Supraventricular tachycardia
+BMGC_DS02413,BMG_DS003126,Takayasu Arteritis
+BMGC_DS02414,BMG_DS003127,Tangier Disease
+BMGC_DS02415,BMG_DS003128,Tarsal Tunnel Syndrome
+BMGC_DS02416,BMG_DS003129,Taste Disorders
+BMGC_DS02417,BMG_DS003130,Tay-Sachs Disease
+BMGC_DS02418,BMG_DS003131,Hereditary hemorrhagic telangiectasia
+BMGC_DS02419,BMG_DS003132,telangiectasis
+BMGC_DS02420,BMG_DS003133,Giant Cell Arteritis
+BMGC_DS02421,BMG_DS003135,Temporomandibular Joint Disorders
+BMGC_DS02422,BMG_DS003136,Temporomandibular Joint Dysfunction Syndrome
+BMGC_DS02423,BMG_DS003137,Tendinitis
+BMGC_DS02424,BMG_DS003138,Tennis Elbow
+BMGC_DS02425,BMG_DS003139,Tenosynovitis
+BMGC_DS02426,BMG_DS003140,teratoma
+BMGC_DS02427,BMG_DS003141,Testicular Diseases
+BMGC_DS02428,BMG_DS003142,Androgen-Insensitivity Syndrome
+BMGC_DS02429,BMG_DS003143,neoplasm of testis
+BMGC_DS02430,BMG_DS003144,Tetanic cataract
+BMGC_DS02431,BMG_DS003145,Tetanus
+BMGC_DS02432,BMG_DS003146,tetralogy of fallot
+BMGC_DS02433,BMG_DS003147,Thalamic Diseases
+BMGC_DS02434,BMG_DS003148,Thalassemia
+BMGC_DS02435,BMG_DS003149,Thanatophoric Dysplasia
+BMGC_DS02436,BMG_DS003151,Theileriasis
+BMGC_DS02437,BMG_DS003152,Thiamine Deficiency
+BMGC_DS02438,BMG_DS003154,Thoracic Diseases
+BMGC_DS02439,BMG_DS003155,neoplasm of thorax
+BMGC_DS02440,BMG_DS003156,Thoracic Outlet Syndrome
+BMGC_DS02441,BMG_DS003157,Thrombasthenia
+BMGC_DS02442,BMG_DS003158,Thromboangiitis Obliterans
+BMGC_DS02443,BMG_DS003159,"Thrombocythemia, Essential"
+BMGC_DS02444,BMG_DS003160,Thrombocytopenia
+BMGC_DS02445,BMG_DS003161,thrombophlebitis
+BMGC_DS02446,BMG_DS003162,thrombotic disease
+BMGC_DS02447,BMG_DS003164,thymoma
+BMGC_DS02448,BMG_DS003165,Thymus Hyperplasia
+BMGC_DS02449,BMG_DS003167,Thyroid Crisis
+BMGC_DS02450,BMG_DS003168,Thyroid Diseases
+BMGC_DS02451,BMG_DS003169,thyroid tumor
+BMGC_DS02452,BMG_DS003170,Thyroiditis
+BMGC_DS02453,BMG_DS003171,Subacute thyroiditis
+BMGC_DS02454,BMG_DS003172,"Thyroiditis, Suppurative"
+BMGC_DS02455,BMG_DS003173,Thyrotoxicosis
+BMGC_DS02456,BMG_DS003174,tic disorder
+BMGC_DS02457,BMG_DS003175,Tick Infestations
+BMGC_DS02458,BMG_DS003176,Tick Paralysis
+BMGC_DS02459,BMG_DS003179,Tietze's Syndrome
+BMGC_DS02460,BMG_DS003180,Tinea
+BMGC_DS02461,BMG_DS003181,White Piedra
+BMGC_DS02462,BMG_DS003182,Tinea Capitis
+BMGC_DS02463,BMG_DS003183,Tinea corporis (disorder)
+BMGC_DS02464,BMG_DS003185,Tinea Favosa
+BMGC_DS02465,BMG_DS003187,Tinea Pedis
+BMGC_DS02466,BMG_DS003188,Onychomycosis
+BMGC_DS02467,BMG_DS003189,Tinea Versicolor
+BMGC_DS02468,BMG_DS003190,Tinnitus
+BMGC_DS02469,BMG_DS003192,Tolosa-Hunt Syndrome
+BMGC_DS02470,BMG_DS003193,Tongue Diseases
+BMGC_DS02471,BMG_DS003194,tongue neoplasm
+BMGC_DS02472,BMG_DS003195,fissured tongue
+BMGC_DS02473,BMG_DS003196,Hairy tongue
+BMGC_DS02474,BMG_DS003198,Tonsillitis
+BMGC_DS02475,BMG_DS003199,Tooth Diseases
+BMGC_DS02476,BMG_DS003200,Tooth Erosion
+BMGC_DS02477,BMG_DS003202,Tooth Resorption
+BMGC_DS02478,BMG_DS003204,"teeth, supernumerary"
+BMGC_DS02479,BMG_DS003205,Torsades de Pointes
+BMGC_DS02480,BMG_DS003206,inherited torticollis
+BMGC_DS02481,BMG_DS003207,Gilles de la Tourette syndrome
+BMGC_DS02482,BMG_DS003208,Toxascariasis
+BMGC_DS02483,BMG_DS003209,Toxocariasis
+BMGC_DS02484,BMG_DS003210,Toxoplasmosis
+BMGC_DS02485,BMG_DS003212,"Toxoplasmosis, Congenital"
+BMGC_DS02486,BMG_DS003215,Tracheal Diseases
+BMGC_DS02487,BMG_DS003217,Tracheal Stenosis
+BMGC_DS02488,BMG_DS003218,Tracheitis
+BMGC_DS02489,BMG_DS003220,Tracheobronchomegaly
+BMGC_DS02490,BMG_DS003221,esophageal atresia/tracheoesophageal fistula
+BMGC_DS02491,BMG_DS003222,Trachoma
+BMGC_DS02492,BMG_DS003224,adjustment disorder
+BMGC_DS02493,BMG_DS003225,transient tic disorder
+BMGC_DS02494,BMG_DS003226,transposition of the great arteries
+BMGC_DS02495,BMG_DS003227,transvestism
+BMGC_DS02496,BMG_DS003230,Trench Fever
+BMGC_DS02497,BMG_DS003233,Trichinellosis
+BMGC_DS02498,BMG_DS003234,Trichomonas Infections
+BMGC_DS02499,BMG_DS003235,Trichomonas Vaginitis
+BMGC_DS02500,BMG_DS003239,Trichophytosis
+BMGC_DS02501,BMG_DS003240,Trichostrongyloidiasis
+BMGC_DS02502,BMG_DS003241,Trichostrongylosis
+BMGC_DS02503,BMG_DS003242,trichotillomania
+BMGC_DS02504,BMG_DS003243,Infection by Trichuris trichiura
+BMGC_DS02505,BMG_DS003244,Tricuspid Valve Insufficiency
+BMGC_DS02506,BMG_DS003245,Tricuspid Valve Prolapse
+BMGC_DS02507,BMG_DS003246,Tricuspid Valve Stenosis
+BMGC_DS02508,BMG_DS003247,Trigeminal Neuralgia
+BMGC_DS02509,BMG_DS003248,Trismus
+BMGC_DS02510,BMG_DS003250,Trombiculiasis
+BMGC_DS02511,BMG_DS003251,trophoblastic neoplasm
+BMGC_DS02512,BMG_DS003252,Tropical pyomyositis
+BMGC_DS02513,BMG_DS003253,persistent truncus arteriosus
+BMGC_DS02514,BMG_DS003254,Trypanosomiasis
+BMGC_DS02515,BMG_DS003255,African Trypanosomiasis
+BMGC_DS02516,BMG_DS003259,Chagas Disease
+BMGC_DS02517,BMG_DS003261,Tuberculoma
+BMGC_DS02518,BMG_DS003262,Tuberculosis
+BMGC_DS02519,BMG_DS003265,"Tuberculosis, Bovine"
+BMGC_DS02520,BMG_DS003266,"Tuberculosis, Cardiovascular"
+BMGC_DS02521,BMG_DS003267,"Tuberculosis, Cutaneous"
+BMGC_DS02522,BMG_DS003270,"Tuberculosis, Gastrointestinal"
+BMGC_DS02523,BMG_DS003271,"Tuberculosis, Hepatic"
+BMGC_DS02524,BMG_DS003272,"Tuberculosis, Laryngeal"
+BMGC_DS02525,BMG_DS003275,"Tuberculosis, Meningeal"
+BMGC_DS02526,BMG_DS003276,"Tuberculosis, Miliary"
+BMGC_DS02527,BMG_DS003277,"Tuberculosis, Ocular"
+BMGC_DS02528,BMG_DS003278,"Tuberculosis, Oral"
+BMGC_DS02529,BMG_DS003280,"Peritonitis, Tuberculous"
+BMGC_DS02530,BMG_DS003281,Pleural Tuberculosis
+BMGC_DS02531,BMG_DS003282,"Tuberculosis, Pulmonary"
+BMGC_DS02532,BMG_DS003283,"Tuberculosis, Renal"
+BMGC_DS02533,BMG_DS003284,"Tuberculosis, Spinal"
+BMGC_DS02534,BMG_DS003287,"Tuberculosis, Urogenital"
+BMGC_DS02535,BMG_DS003289,tuberous sclerosis
+BMGC_DS02536,BMG_DS003290,Tubo-ovarian abscess
+BMGC_DS02537,BMG_DS003291,"Nephritis, Tubulointerstitial"
+BMGC_DS02538,BMG_DS003292,Tularemia
+BMGC_DS02539,BMG_DS003293,Tumor Lysis Syndrome
+BMGC_DS02540,BMG_DS003294,Turner Syndrome
+BMGC_DS02541,BMG_DS003295,"Turner Syndrome, Male"
+BMGC_DS02542,BMG_DS003297,Typhoid Fever
+BMGC_DS02543,BMG_DS003298,typhus
+BMGC_DS02544,BMG_DS003299,Endemic Flea-Borne Typhus
+BMGC_DS02545,BMG_DS003300,"Typhus, Epidemic Louse-Borne"
+BMGC_DS02546,BMG_DS003301,ulcer disease
+BMGC_DS02547,BMG_DS003304,Infection by Uncinaria
+BMGC_DS02548,BMG_DS003305,attention deficit hyperactivity disorder
+BMGC_DS02549,BMG_DS003306,melancholic depression
+BMGC_DS02550,BMG_DS003309,immune system disease
+BMGC_DS02551,BMG_DS003310,Disorder of tympanic membrane
+BMGC_DS02552,BMG_DS003311,Erythema
+BMGC_DS02553,BMG_DS003312,internal hemorrhoid
+BMGC_DS02554,BMG_DS003313,dissociative disorder
+BMGC_DS02555,BMG_DS003314,toxic pneumonitis
+BMGC_DS02556,BMG_DS003315,Upper Respiratory Infections
+BMGC_DS02557,BMG_DS003316,urachal cyst
+BMGC_DS02558,BMG_DS003317,Uremia
+BMGC_DS02559,BMG_DS003318,Ureterolithiasis
+BMGC_DS02560,BMG_DS003319,ureter neoplasm
+BMGC_DS02561,BMG_DS003322,ureterocele
+BMGC_DS02562,BMG_DS003323,Urethral Diseases
+BMGC_DS02563,BMG_DS003324,urethra neoplasm
+BMGC_DS02564,BMG_DS003325,Urethral Obstruction
+BMGC_DS02565,BMG_DS003326,Urethral Stenosis
+BMGC_DS02566,BMG_DS003327,Urethritis
+BMGC_DS02567,BMG_DS003328,Urinary Stress Incontinence
+BMGC_DS02568,BMG_DS003329,Urinary tract infection
+BMGC_DS02569,BMG_DS003331,Urination Disorders
+BMGC_DS02570,BMG_DS003332,Urologic Diseases
+BMGC_DS02571,BMG_DS003333,urinary system neoplasm
+BMGC_DS02572,BMG_DS003334,Urticaria
+BMGC_DS02573,BMG_DS003335,maculopapular cutaneous mastocytosis
+BMGC_DS02574,BMG_DS003336,Uterine Diseases
+BMGC_DS02575,BMG_DS003337,uterine corpus leiomyoma
+BMGC_DS02576,BMG_DS003339,tumor of uterus
+BMGC_DS02577,BMG_DS003341,Uveal Diseases
+BMGC_DS02578,BMG_DS003343,Uveitis
+BMGC_DS02579,BMG_DS003344,Anterior uveitis
+BMGC_DS02580,BMG_DS003345,"Uveitis, Intermediate"
+BMGC_DS02581,BMG_DS003346,"Uveitis, Posterior"
+BMGC_DS02582,BMG_DS003347,"Uveitis, Suppurative"
+BMGC_DS02583,BMG_DS003348,Uveomeningoencephalitic Syndrome
+BMGC_DS02584,BMG_DS003349,Uveoparotid Fever
+BMGC_DS02585,BMG_DS003351,Vaccinia
+BMGC_DS02586,BMG_DS003354,vaginal cancer
+BMGC_DS02587,BMG_DS003355,Vaginal Diseases
+BMGC_DS02588,BMG_DS003356,vaginal neoplasm
+BMGC_DS02589,BMG_DS003357,psychologic vaginismus
+BMGC_DS02590,BMG_DS003358,Vaginitis
+BMGC_DS02591,BMG_DS003359,Vaginitis and vulvovaginitis
+BMGC_DS02592,BMG_DS003360,Migraine Variant
+BMGC_DS02593,BMG_DS003361,Varicocele
+BMGC_DS02594,BMG_DS003362,Varicose Ulcer
+BMGC_DS02595,BMG_DS003363,varicose disease
+BMGC_DS02596,BMG_DS003366,conjunctival vascular disorder
+BMGC_DS02597,BMG_DS003367,Vascular Diseases
+BMGC_DS02598,BMG_DS003368,Male genital organ vascular diseases
+BMGC_DS02599,BMG_DS003369,Vascular Headaches
+BMGC_DS02600,BMG_DS003370,Vasculitis
+BMGC_DS02601,BMG_DS003371,"Vasculitis, Hemorrhagic"
+BMGC_DS02602,BMG_DS003374,Velopharyngeal Insufficiency
+BMGC_DS02603,BMG_DS003376,Venous Insufficiency
+BMGC_DS02604,BMG_DS003377,Ventricular Fibrillation
+BMGC_DS02605,BMG_DS003378,Ventricular Outflow Obstruction
+BMGC_DS02606,BMG_DS003379,"Tachycardia, Ventricular"
+BMGC_DS02607,BMG_DS003380,Plantar wart
+BMGC_DS02608,BMG_DS003382,Vertebral Artery Insufficiency
+BMGC_DS02609,BMG_DS003383,Vertebrobasilar Insufficiency
+BMGC_DS02610,BMG_DS003384,Vesico-Ureteral Reflux
+BMGC_DS02611,BMG_DS003387,Seminal vesiculitis
+BMGC_DS02612,BMG_DS003388,Vestibular Diseases
+BMGC_DS02613,BMG_DS003389,Vibrio Infections
+BMGC_DS02614,BMG_DS003390,"Neuralgia, Vidian"
+BMGC_DS02615,BMG_DS003394,Viremia
+BMGC_DS02616,BMG_DS003395,Virus Diseases
+BMGC_DS02617,BMG_DS003396,Visceral Myopathy
+BMGC_DS02618,BMG_DS003398,vision disorder
+BMGC_DS02619,BMG_DS003400,Low Vision
+BMGC_DS02620,BMG_DS003401,Vitamin A Deficiency
+BMGC_DS02621,BMG_DS003402,Vitamin B 12 Deficiency
+BMGC_DS02622,BMG_DS003403,Vitamin B Deficiency
+BMGC_DS02623,BMG_DS003404,Vitamin D Deficiency
+BMGC_DS02624,BMG_DS003405,Vitamin E Deficiency
+BMGC_DS02625,BMG_DS003406,Vitamin K Deficiency
+BMGC_DS02626,BMG_DS003407,Vitiligo
+BMGC_DS02627,BMG_DS003409,Vitreous abscess
+BMGC_DS02628,BMG_DS003410,Vitreous Detachment
+BMGC_DS02629,BMG_DS003413,Voice Disorders
+BMGC_DS02630,BMG_DS003414,Volkmann Contracture
+BMGC_DS02631,BMG_DS003415,Intestinal Volvulus
+BMGC_DS02632,BMG_DS003416,von Willebrand Disease
+BMGC_DS02633,BMG_DS003418,Vulvar Diseases
+BMGC_DS02634,BMG_DS003419,vulvar neoplasm
+BMGC_DS02635,BMG_DS003420,Vulvitis
+BMGC_DS02636,BMG_DS003421,Vulvovaginitis
+BMGC_DS02637,BMG_DS003422,Lateral Medullary Syndrome
+BMGC_DS02638,BMG_DS003423,Wallerian degeneration
+BMGC_DS02639,BMG_DS003424,common wart
+BMGC_DS02640,BMG_DS003425,Wasting Syndrome
+BMGC_DS02641,BMG_DS003426,Water Intoxication
+BMGC_DS02642,BMG_DS003427,Waterhouse-Friderichsen Syndrome
+BMGC_DS02643,BMG_DS003429,HMN (Hereditary Motor Neuropathy) Proximal Type I
+BMGC_DS02644,BMG_DS003430,Werner Syndrome
+BMGC_DS02645,BMG_DS003431,Wernicke Encephalopathy
+BMGC_DS02646,BMG_DS003432,West Nile Fever
+BMGC_DS02647,BMG_DS003435,Dental White Spot
+BMGC_DS02648,BMG_DS003436,Pertussis
+BMGC_DS02649,BMG_DS003438,Wiskott-Aldrich Syndrome
+BMGC_DS02650,BMG_DS003439,Wissler's Syndrome
+BMGC_DS02651,BMG_DS003440,Wolff-Parkinson-White Syndrome
+BMGC_DS02652,BMG_DS003441,Wolfram Syndrome
+BMGC_DS02653,BMG_DS003442,Wolman Disease
+BMGC_DS02654,BMG_DS003444,juvenile xanthogranuloma
+BMGC_DS02655,BMG_DS003445,Xanthomatosis
+BMGC_DS02656,BMG_DS003446,Xeroderma
+BMGC_DS02657,BMG_DS003447,xeroderma pigmentosum
+BMGC_DS02658,BMG_DS003448,Xerophthalmia
+BMGC_DS02659,BMG_DS003449,Xerostomia
+BMGC_DS02660,BMG_DS003450,Yaws
+BMGC_DS02661,BMG_DS003451,Yellow Fever
+BMGC_DS02662,BMG_DS003454,Yersinia pseudotuberculosis Infections
+BMGC_DS02663,BMG_DS003455,Zellweger Syndrome
+BMGC_DS02664,BMG_DS003456,Zollinger-Ellison syndrome
+BMGC_DS02665,BMG_DS003458,Zygomycosis
+BMGC_DS02666,BMG_DS003459,Accelerated Idioventricular Rhythm
+BMGC_DS02667,BMG_DS003461,ocular albinism
+BMGC_DS02668,BMG_DS003462,oculocutaneous albinism
+BMGC_DS02669,BMG_DS003463,Arachnoid Cysts
+BMGC_DS02670,BMG_DS003465,Cerebral Thrombosis
+BMGC_DS02671,BMG_DS003466,Cockayne-Touraine Disease
+BMGC_DS02672,BMG_DS003467,"Hyperkeratosis, Epidermolytic"
+BMGC_DS02673,BMG_DS003468,Congenital Nonbullous Ichthyosiform Erythroderma
+BMGC_DS02674,BMG_DS003470,desmoid tumor
+BMGC_DS02675,BMG_DS003472,Epidermolysis Bullosa Acquisita
+BMGC_DS02676,BMG_DS003473,Epidermolysis Bullosa Dystrophica
+BMGC_DS02677,BMG_DS003474,Epidermolysis Bullosa Herpetiformis Dowling-Meara
+BMGC_DS02678,BMG_DS003475,Epidermolysis Bullosa Progressiva
+BMGC_DS02679,BMG_DS003476,Epidermolysis Bullosa Simplex
+BMGC_DS02680,BMG_DS003477,Junctional Epidermolysis Bullosa
+BMGC_DS02681,BMG_DS003479,Hallopeau-Siemens Disease
+BMGC_DS02682,BMG_DS003480,Heart Valve Prolapse
+BMGC_DS02683,BMG_DS003481,Helicobacter Infections
+BMGC_DS02684,BMG_DS003482,Hermanski-Pudlak Syndrome
+BMGC_DS02685,BMG_DS003483,holoprosencephaly
+BMGC_DS02686,BMG_DS003484,"Ichthyosiform Erythroderma, Congenital"
+BMGC_DS02687,BMG_DS003485,Ichthyosis Vulgaris
+BMGC_DS02688,BMG_DS003486,"Ichthyosis, X-Linked"
+BMGC_DS02689,BMG_DS003487,Klein's Syndrome
+BMGC_DS02690,BMG_DS003488,Lentivirus Infections
+BMGC_DS02691,BMG_DS003489,Herlitz Disease
+BMGC_DS02692,BMG_DS003490,B-cell neoplasm
+BMGC_DS02693,BMG_DS003491,diffuse large B-cell lymphoma
+BMGC_DS02694,BMG_DS003494,T-cell non-Hodgkin lymphoma
+BMGC_DS02695,BMG_DS003495,primary cutaneous T-cell lymphoma
+BMGC_DS02696,BMG_DS003496,primary cutaneous peripheral T-cell lymphoma not otherwise specified
+BMGC_DS02697,BMG_DS003497,milk allergy
+BMGC_DS02698,BMG_DS003498,oligohydramnios
+BMGC_DS02699,BMG_DS003502,piebaldism
+BMGC_DS02700,BMG_DS003504,Postpoliomyelitis Syndrome
+BMGC_DS02701,BMG_DS003506,Vesicular Skin Diseases
+BMGC_DS02702,BMG_DS003508,spina bifida
+BMGC_DS02703,BMG_DS003509,Tethered Cord Syndrome
+BMGC_DS02704,BMG_DS003512,Weber-Cockayne Syndrome
+BMGC_DS02705,BMG_DS003514,Granuloma Annulare
+BMGC_DS02706,BMG_DS003515,Sweet Syndrome
+BMGC_DS02707,BMG_DS003516,Lysosomal Storage Diseases
+BMGC_DS02708,BMG_DS003517,Fungemia
+BMGC_DS02709,BMG_DS003518,Ovarian Hyperstimulation Syndrome
+BMGC_DS02710,BMG_DS003519,Motor Neuron Disease
+BMGC_DS02711,BMG_DS003520,Peripheral Vascular Diseases
+BMGC_DS02712,BMG_DS003521,Familial benign pemphigus
+BMGC_DS02713,BMG_DS003522,Corneal Neovascularization
+BMGC_DS02714,BMG_DS003523,Severe Combined Immunodeficiency
+BMGC_DS02715,BMG_DS003524,Foot Ulcer
+BMGC_DS02716,BMG_DS003525,Bronchial Hyperreactivity
+BMGC_DS02717,BMG_DS003526,Gangliosidosis GM1
+BMGC_DS02718,BMG_DS003527,Mucopolysaccharidosis VII
+BMGC_DS02719,BMG_DS003528,central nervous system neoplasm
+BMGC_DS02720,BMG_DS003529,choroid plexus neoplasm
+BMGC_DS02721,BMG_DS003530,seasonal affective disorder
+BMGC_DS02722,BMG_DS003531,Hidradenitis
+BMGC_DS02723,BMG_DS003532,Bacterial Vaginosis
+BMGC_DS02724,BMG_DS003533,granular cell tumor
+BMGC_DS02725,BMG_DS003534,Eosinophilia-Myalgia Syndrome
+BMGC_DS02726,BMG_DS003535,Gestational Diabetes
+BMGC_DS02727,BMG_DS003536,"Encephalopathy, Bovine Spongiform"
+BMGC_DS02728,BMG_DS003537,"Ovarian Failure, Premature"
+BMGC_DS02729,BMG_DS003538,Cerebral Amyloid Angiopathy
+BMGC_DS02730,BMG_DS003539,Psoas Abscess
+BMGC_DS02731,BMG_DS003541,Adult-Onset Still Disease
+BMGC_DS02732,BMG_DS003542,Proteus syndrome
+BMGC_DS02733,BMG_DS003543,pulmonary plasma cell granuloma
+BMGC_DS02734,BMG_DS003544,Orbital Pseudotumor
+BMGC_DS02735,BMG_DS003545,Erythema Infectiosum
+BMGC_DS02736,BMG_DS003547,Antiphospholipid Syndrome
+BMGC_DS02737,BMG_DS003548,Alagille syndrome
+BMGC_DS02738,BMG_DS003549,Stiff-Person Syndrome
+BMGC_DS02739,BMG_DS003550,Hepatitis E
+BMGC_DS02740,BMG_DS003552,Embolism and Thrombosis
+BMGC_DS02741,BMG_DS003553,Ciliophora Infections
+BMGC_DS02742,BMG_DS003556,"Toxoplasmosis, Cerebral"
+BMGC_DS02743,BMG_DS003559,Li-Fraumeni Syndrome
+BMGC_DS02744,BMG_DS003561,Serratia Infections
+BMGC_DS02745,BMG_DS003563,Neisseriaceae Infections
+BMGC_DS02746,BMG_DS003564,Pasteurellaceae Infections
+BMGC_DS02747,BMG_DS003565,Ehrlichiosis
+BMGC_DS02748,BMG_DS003566,POEMS Syndrome
+BMGC_DS02749,BMG_DS003567,Microsporidiosis
+BMGC_DS02750,BMG_DS003568,"Polyendocrinopathies, Autoimmune"
+BMGC_DS02751,BMG_DS003569,Angiodysplasia
+BMGC_DS02752,BMG_DS003570,Encephalitozoonosis
+BMGC_DS02753,BMG_DS003571,"Polycystic Kidney, Autosomal Dominant"
+BMGC_DS02754,BMG_DS003572,"Epilepsy, Complex Partial"
+BMGC_DS02755,BMG_DS003573,Gram-Negative Bacterial Infections
+BMGC_DS02756,BMG_DS003574,Gram-Positive Bacterial Infections
+BMGC_DS02757,BMG_DS003575,"Angiomatosis, Bacillary"
+BMGC_DS02758,BMG_DS003576,"Arthritis, Reactive"
+BMGC_DS02759,BMG_DS003577,"Meningitis, Cryptococcal"
+BMGC_DS02760,BMG_DS003578,"Meningitis, Bacterial"
+BMGC_DS02761,BMG_DS003579,"Meningitis, Fungal"
+BMGC_DS02762,BMG_DS003581,"Epilepsy, Frontal Lobe"
+BMGC_DS02763,BMG_DS003583,"Phenylketonuria, Maternal"
+BMGC_DS02764,BMG_DS003584,Autosomal Recessive Polycystic Kidney Disease
+BMGC_DS02765,BMG_DS003585,Buruli Ulcer
+BMGC_DS02766,BMG_DS003586,"Metabolic acidosis, NAG, acidifying salts"
+BMGC_DS02767,BMG_DS003588,Palindromic rheumatism
+BMGC_DS02768,BMG_DS003589,Iron-Refractory Iron Deficiency Anemia
+BMGC_DS02769,BMG_DS003590,Normocytic anemia
+BMGC_DS02770,BMG_DS003591,Thalassemia Minor
+BMGC_DS02771,BMG_DS003592,Essential Hypertension
+BMGC_DS02772,BMG_DS003594,Retrobulbar Neuritis
+BMGC_DS02773,BMG_DS003595,Choreoathetosis
+BMGC_DS02774,BMG_DS003596,Encephalopathies
+BMGC_DS02775,BMG_DS003598,Liver Failure
+BMGC_DS02776,BMG_DS003599,Ventricular arrhythmia
+BMGC_DS02777,BMG_DS003600,First degree atrioventricular block
+BMGC_DS02778,BMG_DS003601,Right bundle branch block
+BMGC_DS02779,BMG_DS003602,Monoplegia
+BMGC_DS02780,BMG_DS003604,oculogyric crisis
+BMGC_DS02781,BMG_DS003605,Livedo Reticularis
+BMGC_DS02782,BMG_DS003606,Purpura Fulminans
+BMGC_DS02783,BMG_DS003607,Pyoderma Gangrenosum
+BMGC_DS02784,BMG_DS003608,pyogenic granuloma
+BMGC_DS02785,BMG_DS003609,Polymyositis
+BMGC_DS02786,BMG_DS003610,Nummular eczema
+BMGC_DS02787,BMG_DS003619,acute leukemia
+BMGC_DS02788,BMG_DS003620,Alcoholic Neuropathy
+BMGC_DS02789,BMG_DS003621,Hyperchloremia
+BMGC_DS02790,BMG_DS003622,Hypochloremia (disorder)
+BMGC_DS02791,BMG_DS003623,Hyperphosphatemia (disorder)
+BMGC_DS02792,BMG_DS003624,Hypophosphatemia
+BMGC_DS02793,BMG_DS003625,Internal hordeolum
+BMGC_DS02794,BMG_DS003629,Chronic gastritis
+BMGC_DS02795,BMG_DS003631,Chronic pyelonephritis
+BMGC_DS02796,BMG_DS003633,Chondromalacia
+BMGC_DS02797,BMG_DS003635,Mendelson Syndrome
+BMGC_DS02798,BMG_DS003637,breast adenosis
+BMGC_DS02799,BMG_DS003638,alcohol abuse
+BMGC_DS02800,BMG_DS003640,Hamman-Rich syndrome
+BMGC_DS02801,BMG_DS003642,Anguilluliasis
+BMGC_DS02802,BMG_DS003643,Antibiotic-Associated Colitis
+BMGC_DS02803,BMG_DS003644,Polyglandular Type I Autoimmune Syndrome
+BMGC_DS02804,BMG_DS003645,"Autoimmune Syndrome Type II, Polyglandular"
+BMGC_DS02805,BMG_DS003647,Bouillaud Disease
+BMGC_DS02806,BMG_DS003648,Brachial Neuralgia
+BMGC_DS02807,BMG_DS003652,"Eczema, Infantile"
+BMGC_DS02808,BMG_DS003653,Enterobiasis
+BMGC_DS02809,BMG_DS003654,"Epilepsy, Atonic"
+BMGC_DS02810,BMG_DS003655,"Epilepsy, Cryptogenic"
+BMGC_DS02811,BMG_DS003657,"Epilepsy, Simple Partial"
+BMGC_DS02812,BMG_DS003658,"Epilepsy, Tonic"
+BMGC_DS02813,BMG_DS003659,Essential Polyarteritis
+BMGC_DS02814,BMG_DS003660,Gonadotropin-Resistant Ovary Syndrome
+BMGC_DS02815,BMG_DS003661,Granuloma Gangraenescens
+BMGC_DS02816,BMG_DS003662,Hereditary Sensory Radicular Neuropathy
+BMGC_DS02817,BMG_DS003663,Hurler-Scheie Syndrome
+BMGC_DS02818,BMG_DS003664,"Hyalinosis, Segmental Glomerular"
+BMGC_DS02819,BMG_DS003665,Hypogammaglobulinemia
+BMGC_DS02820,BMG_DS003666,Idiopathic Membranous Glomerulonephritis
+BMGC_DS02821,BMG_DS003667,Industrial Dermatosis
+BMGC_DS02822,BMG_DS003669,"Leishmaniasis, New World"
+BMGC_DS02823,BMG_DS003671,Cataract
+BMGC_DS02824,BMG_DS003674,Marasmus
+BMGC_DS02825,BMG_DS003675,Minamata Disease
+BMGC_DS02826,BMG_DS003676,Mucopolysaccharidosis Type IIIA
+BMGC_DS02827,BMG_DS003677,Mucopolysaccharidosis Type IIIB
+BMGC_DS02828,BMG_DS003678,MPS III C
+BMGC_DS02829,BMG_DS003679,MPS III D
+BMGC_DS02830,BMG_DS003680,"Mucopolysaccharidosis, MPS-IV-A"
+BMGC_DS02831,BMG_DS003681,Mucopolysaccharidosis type IVB
+BMGC_DS02832,BMG_DS003682,myelomeningocele
+BMGC_DS02833,BMG_DS003683,Myocardial Preinfarction Syndrome
+BMGC_DS02834,BMG_DS003684,benign neoplasm
+BMGC_DS02835,BMG_DS003685,Osteoarthrosis Deformans
+BMGC_DS02836,BMG_DS003686,pancreatic cholera
+BMGC_DS02837,BMG_DS003687,paroxysmal cold hemoglobinuria
+BMGC_DS02838,BMG_DS003689,Pfaundler-Hurler Syndrome
+BMGC_DS02839,BMG_DS003690,Plantar Ulcer
+BMGC_DS02840,BMG_DS003691,Pseudopelade
+BMGC_DS02841,BMG_DS003692,Rheumatoid Purpura
+BMGC_DS02842,BMG_DS003696,Sicca Syndrome
+BMGC_DS02843,BMG_DS003697,"Ataxia, Spinocerebellar"
+BMGC_DS02844,BMG_DS003698,Juvenile-Onset Still Disease
+BMGC_DS02845,BMG_DS003701,Acute dacryoadenitis
+BMGC_DS02846,BMG_DS003702,Chronic dacryocystitis
+BMGC_DS02847,BMG_DS003703,Orbital Cellulitis
+BMGC_DS02848,BMG_DS003705,Acute sinusitis
+BMGC_DS02849,BMG_DS003706,Acute tracheitis
+BMGC_DS02850,BMG_DS003707,Acute bronchitis
+BMGC_DS02851,BMG_DS003708,Chronic sinusitis
+BMGC_DS02852,BMG_DS003709,Chronic tonsillitis
+BMGC_DS02853,BMG_DS003711,Chronic Persistent Hepatitis
+BMGC_DS02854,BMG_DS003713,"Pancreatitis, Chronic"
+BMGC_DS02855,BMG_DS003715,Acute cystitis
+BMGC_DS02856,BMG_DS003717,Calculus of prostate
+BMGC_DS02857,BMG_DS003718,Allergic urticaria
+BMGC_DS02858,BMG_DS003719,Congenital heart block
+BMGC_DS02859,BMG_DS003721,"Neurogenic Urinary Bladder, Atonic"
+BMGC_DS02860,BMG_DS003725,cecum carcinoma
+BMGC_DS02861,BMG_DS003726,Cervical lymphadenitis
+BMGC_DS02862,BMG_DS003728,Cholesterol Embolism
+BMGC_DS02863,BMG_DS003731,conduct disorder
+BMGC_DS02864,BMG_DS003732,Disorder of carbohydrate metabolism
+BMGC_DS02865,BMG_DS003733,Epstein-Barr Virus Infections
+BMGC_DS02866,BMG_DS003735,Gingivostomatitis
+BMGC_DS02867,BMG_DS003736,Left Ventricular Hypertrophy
+BMGC_DS02868,BMG_DS003737,Lower respiratory tract infection
+BMGC_DS02869,BMG_DS003738,Oral Ulcer
+BMGC_DS02870,BMG_DS003740,"Fasciitis, Plantar"
+BMGC_DS02871,BMG_DS003746,Spontaneous pneumothorax
+BMGC_DS02872,BMG_DS003747,squamous cell lung carcinoma
+BMGC_DS02873,BMG_DS003754,Hypertrophy of adenoids
+BMGC_DS02874,BMG_DS003760,bronchus adenoma
+BMGC_DS02875,BMG_DS003761,Achilles bursitis
+BMGC_DS02876,BMG_DS003766,Spasmodic Croup
+BMGC_DS02877,BMG_DS003767,De Quervain Disease
+BMGC_DS02878,BMG_DS003768,Deep Vein Thrombosis
+BMGC_DS02879,BMG_DS003770,hypoglycemic encephalopathy
+BMGC_DS02880,BMG_DS003773,Epididymo-orchitis
+BMGC_DS02881,BMG_DS003775,"Seizure, Febrile, Simple"
+BMGC_DS02882,BMG_DS003776,Slipped Capital Femoral Epiphyses
+BMGC_DS02883,BMG_DS003778,Secondary glaucoma
+BMGC_DS02884,BMG_DS003780,Cholestatic hepatitis
+BMGC_DS02885,BMG_DS003783,Humoral hypercalcemia of malignancy (disorder)
+BMGC_DS02886,BMG_DS003784,Lichen Simplex Chronicus
+BMGC_DS02887,BMG_DS003785,small cell lung carcinoma
+BMGC_DS02888,BMG_DS003787,Migraine Disorders
+BMGC_DS02889,BMG_DS003788,Obstructive nephropathy
+BMGC_DS02890,BMG_DS003789,Sciatic Neuropathy
+BMGC_DS02891,BMG_DS003791,Acute otitis externa
+BMGC_DS02892,BMG_DS003792,ovarian fibroma
+BMGC_DS02893,BMG_DS003793,annular pancreas
+BMGC_DS02894,BMG_DS003799,Gonorrhea of pharynx
+BMGC_DS02895,BMG_DS003803,rectum adenocarcinoma
+BMGC_DS02896,BMG_DS003806,"Syphilis, secondary"
+BMGC_DS02897,BMG_DS003816,Chronic Headache
+BMGC_DS02898,BMG_DS003817,Mononeuritis Multiplex
+BMGC_DS02899,BMG_DS003818,Cranial nerve palsies
+BMGC_DS02900,BMG_DS003819,Sensory neuropathy
+BMGC_DS02901,BMG_DS003820,Chronic Infection
+BMGC_DS02902,BMG_DS003822,Active tuberculosis
+BMGC_DS02903,BMG_DS003825,"Vasculitis, Leukocytoclastic, Cutaneous"
+BMGC_DS02904,BMG_DS003832,Addisonian crisis
+BMGC_DS02905,BMG_DS003833,thyroid adenoma
+BMGC_DS02906,BMG_DS003834,Hypochloremic alkalosis
+BMGC_DS02907,BMG_DS003835,Megaloblastic anemia due to folate deficiency
+BMGC_DS02908,BMG_DS003837,Atrophic condition of skin
+BMGC_DS02909,BMG_DS003838,Thyroid Hypoplasia
+BMGC_DS02910,BMG_DS003839,Complete atrioventricular block
+BMGC_DS02911,BMG_DS003841,digestive system carcinoma
+BMGC_DS02912,BMG_DS003843,Central nervous system depression (disorder)
+BMGC_DS02913,BMG_DS003848,Hemorrhagic diarrhea
+BMGC_DS02914,BMG_DS003849,Hypertensive Encephalopathy
+BMGC_DS02915,BMG_DS003850,Endometrial disorder
+BMGC_DS02916,BMG_DS003852,Premature ventricular contractions
+BMGC_DS02917,BMG_DS003853,Fanconi like syndrome
+BMGC_DS02918,BMG_DS003854,Renal fibrosis
+BMGC_DS02919,BMG_DS003857,Gastrointestinal perforation
+BMGC_DS02920,BMG_DS003859,hypoalphalipoproteinemia
+BMGC_DS02921,BMG_DS003860,Hypermagnesemia
+BMGC_DS02922,BMG_DS003861,Hypocholesterolemia
+BMGC_DS02923,BMG_DS003862,Testicular hypogonadism
+BMGC_DS02924,BMG_DS003863,Hypomagnesemia
+BMGC_DS02925,BMG_DS003864,Hepatic Infarction
+BMGC_DS02926,BMG_DS003865,intracranial hypertension
+BMGC_DS02927,BMG_DS003866,Myocardial Ischemia
+BMGC_DS02928,BMG_DS003867,Renal tubular disorder
+BMGC_DS02929,BMG_DS003868,Bone marrow depression
+BMGC_DS02930,BMG_DS003869,cutaneous melanoma
+BMGC_DS02931,BMG_DS003870,Disease of mucous membrane
+BMGC_DS02932,BMG_DS003873,Hepatic necrosis
+BMGC_DS02933,BMG_DS003874,Coronary Occlusion
+BMGC_DS02934,BMG_DS003875,Perforated corneal ulcer
+BMGC_DS02935,BMG_DS003877,Pleocytosis
+BMGC_DS02936,BMG_DS003880,Porphyruria
+BMGC_DS02937,BMG_DS003881,Disorder of pregnancy
+BMGC_DS02938,BMG_DS003883,Fungal infection of lung
+BMGC_DS02939,BMG_DS003885,hyperreflexia
+BMGC_DS02940,BMG_DS003888,Hypocalcemic tetany
+BMGC_DS02941,BMG_DS003889,Thrombosis of cerebral veins
+BMGC_DS02942,BMG_DS003895,Ulcer of esophagus
+BMGC_DS02943,BMG_DS003896,Ulceration of intestine
+BMGC_DS02944,BMG_DS003900,lung adenocarcinoma
+BMGC_DS02945,BMG_DS003902,carcinoma of esophagus
+BMGC_DS02946,BMG_DS003903,Gastroparesis
+BMGC_DS02947,BMG_DS003904,congenital heart disease
+BMGC_DS02948,BMG_DS003906,Polyneuropathy
+BMGC_DS02949,BMG_DS003907,Retinal Vasculitis
+BMGC_DS02950,BMG_DS003908,Sensory Disorders
+BMGC_DS02951,BMG_DS003910,Borrelia recurrentis Infection
+BMGC_DS02952,BMG_DS003913,Lobomycosis
+BMGC_DS02953,BMG_DS003914,tinea nigra
+BMGC_DS02954,BMG_DS003915,Echinococcus granulosus infection
+BMGC_DS02955,BMG_DS003916,Echinococcus multilocularis infection
+BMGC_DS02956,BMG_DS003918,Infection by Heterophyes heterophyes
+BMGC_DS02957,BMG_DS003919,Ovale malaria
+BMGC_DS02958,BMG_DS003920,Taenia saginata infection
+BMGC_DS02959,BMG_DS003922,Dyshormonogenic goiter
+BMGC_DS02960,BMG_DS003923,Pelvic congestion syndrome
+BMGC_DS02961,BMG_DS003924,Broad ligament laceration syndrome
+BMGC_DS02962,BMG_DS003925,Pustular psoriasis
+BMGC_DS02963,BMG_DS003926,Transient arthropathy
+BMGC_DS02964,BMG_DS003927,Jaccoud's syndrome
+BMGC_DS02965,BMG_DS003928,reactive arthritis
+BMGC_DS02966,BMG_DS003930,Traumatic spondylopathy
+BMGC_DS02967,BMG_DS003934,Juvenile dermatitis herpetiformis
+BMGC_DS02968,BMG_DS003935,Hypermobility syndrome
+BMGC_DS02969,BMG_DS003936,Nezelof's syndrome
+BMGC_DS02970,BMG_DS003937,Patau syndrome
+BMGC_DS02971,BMG_DS003939,Disease of diaphragm
+BMGC_DS02972,BMG_DS003940,Postcholecystectomy Syndrome
+BMGC_DS02973,BMG_DS003941,Hypoplastic Left Heart Syndrome
+BMGC_DS02974,BMG_DS003942,Kyphoscoliotic heart disease
+BMGC_DS02975,BMG_DS003943,Hypertensive heart disease
+BMGC_DS02976,BMG_DS003944,Postmyocardial infarction syndrome
+BMGC_DS02977,BMG_DS003945,Suberosis
+BMGC_DS02978,BMG_DS003946,Juvenile Spinal Muscular Atrophy
+BMGC_DS02979,BMG_DS003948,Foster-Kennedy Syndrome
+BMGC_DS02980,BMG_DS003949,Rheumatic Chorea
+BMGC_DS02981,BMG_DS003950,Lingual-Facial-Buccal Dyskinesia
+BMGC_DS02982,BMG_DS003951,cervical dystonia
+BMGC_DS02983,BMG_DS003953,Drug withdrawal syndrome
+BMGC_DS02984,BMG_DS003954,Solar Retinitis
+BMGC_DS02985,BMG_DS003955,Hypertensive Retinopathy
+BMGC_DS02986,BMG_DS003956,Internuclear Ophthalmoplegia
+BMGC_DS02987,BMG_DS003957,Exophthalmic ophthalmoplegia
+BMGC_DS02988,BMG_DS003958,Low Tension Glaucoma
+BMGC_DS02989,BMG_DS003959,Phacolytic glaucoma
+BMGC_DS02990,BMG_DS003960,Glaucomatocyclitic crisis
+BMGC_DS02991,BMG_DS003962,Pylorospasm
+BMGC_DS02992,BMG_DS003963,Cyclical vomiting syndrome
+BMGC_DS02993,BMG_DS003964,Pancreatic steatorrhea
+BMGC_DS02994,BMG_DS003965,Anal spasm
+BMGC_DS02995,BMG_DS003967,Idiopathic pulmonary hypertension
+BMGC_DS02996,BMG_DS003971,Vagus Nerve Disorder
+BMGC_DS02997,BMG_DS003972,accessory nerve disorder
+BMGC_DS02998,BMG_DS003973,hypoglossal nerve disorder
+BMGC_DS02999,BMG_DS003974,intermittent explosive disorder
+BMGC_DS03000,BMG_DS003976,Stimulus deprivation amblyopia
+BMGC_DS03001,BMG_DS003977,Refractive amblyopia
+BMGC_DS03002,BMG_DS003978,scotoma
+BMGC_DS03003,BMG_DS003979,Regular astigmatism
+BMGC_DS03004,BMG_DS003980,Irregular astigmatism
+BMGC_DS03005,BMG_DS003981,Spasm of accommodation
+BMGC_DS03006,BMG_DS003982,Total internal ophthalmoplegia
+BMGC_DS03007,BMG_DS003983,Disorder of accommodation
+BMGC_DS03008,BMG_DS003984,Achromatopsia
+BMGC_DS03009,BMG_DS003985,acquired night blindness
+BMGC_DS03010,BMG_DS003986,"Strabismus, Comitant"
+BMGC_DS03011,BMG_DS003987,Monocular Esotropia
+BMGC_DS03012,BMG_DS003988,Alternating esotropia
+BMGC_DS03013,BMG_DS003989,Monocular Exotropia
+BMGC_DS03014,BMG_DS003990,Alternating Exotropia
+BMGC_DS03015,BMG_DS003991,Hypotropia
+BMGC_DS03016,BMG_DS003992,cyclotropia
+BMGC_DS03017,BMG_DS003993,Intermittent tropia
+BMGC_DS03018,BMG_DS003998,Esophoria
+BMGC_DS03019,BMG_DS004001,Cyclophoria
+BMGC_DS03020,BMG_DS004003,Paralytic strabismus
+BMGC_DS03021,BMG_DS004004,Parinaud Syndrome
+BMGC_DS03022,BMG_DS004005,Mechanical Strabismus
+BMGC_DS03023,BMG_DS004008,Lagophthalmos
+BMGC_DS03024,BMG_DS004009,Excessive tearing
+BMGC_DS03025,BMG_DS004015,septate uterus
+BMGC_DS03026,BMG_DS004016,lactocele
+BMGC_DS03027,BMG_DS004019,Acne varioliformis
+BMGC_DS03028,BMG_DS004020,Thrombophlebitis migrans
+BMGC_DS03029,BMG_DS004023,Posterior synechiae
+BMGC_DS03030,BMG_DS004024,Pinguecula
+BMGC_DS03031,BMG_DS004026,mature cataract
+BMGC_DS03032,BMG_DS004027,Morgagnian cataract
+BMGC_DS03033,BMG_DS004029,Cystitis cystica
+BMGC_DS03034,BMG_DS004031,Familial erythrocytosis
+BMGC_DS03035,BMG_DS004032,"Hodgkin's lymphoma, mixed cellularity"
+BMGC_DS03036,BMG_DS004033,"Hodgkin's lymphoma, lymphocytic depletion"
+BMGC_DS03037,BMG_DS004034,nodular sclerosis classical Hodgkin lymphoma
+BMGC_DS03038,BMG_DS004035,polycythemia vera
+BMGC_DS03039,BMG_DS004036,subacute monocytic leukemia
+BMGC_DS03040,BMG_DS004037,granulocytic sarcoma
+BMGC_DS03041,BMG_DS004039,ankyloglossia
+BMGC_DS03042,BMG_DS004040,congenital aortic valve stenosis
+BMGC_DS03043,BMG_DS004041,aortic arch interruption
+BMGC_DS03044,BMG_DS004042,congenital aphakia
+BMGC_DS03045,BMG_DS004043,craniorachischisis
+BMGC_DS03046,BMG_DS004044,polydactyly
+BMGC_DS03047,BMG_DS004047,Sprengel deformity
+BMGC_DS03048,BMG_DS004048,Retinoschisis
+BMGC_DS03049,BMG_DS004049,Corneal staphyloma
+BMGC_DS03050,BMG_DS004052,Urethral diverticulum
+BMGC_DS03051,BMG_DS004054,Hydrops of gallbladder
+BMGC_DS03052,BMG_DS004056,Chronic glomerulonephritis
+BMGC_DS03053,BMG_DS004057,Fibrosis of pericardium
+BMGC_DS03054,BMG_DS004059,Keratomalacia
+BMGC_DS03055,BMG_DS004060,Cholesterolosis of gallbladder
+BMGC_DS03056,BMG_DS004061,Kayser-Fleischer ring
+BMGC_DS03057,BMG_DS004062,Leukocoria
+BMGC_DS03058,BMG_DS004063,Balanitis xerotica obliterans
+BMGC_DS03059,BMG_DS004065,Salmonella sepsis
+BMGC_DS03060,BMG_DS004072,Acute amebiasis
+BMGC_DS03061,BMG_DS004073,Chronic intestinal amebiasis
+BMGC_DS03062,BMG_DS004079,Other specified protozoal intestinal diseases
+BMGC_DS03063,BMG_DS004080,Intestinal infection caused by Pseudomonas
+BMGC_DS03064,BMG_DS004081,Bacterial enteritis
+BMGC_DS03065,BMG_DS004082,Viral gastroenteritis
+BMGC_DS03066,BMG_DS004086,Tuberculous pleurisy in primary progressive tuberculosis
+BMGC_DS03067,BMG_DS004094,Tuberculous pneumothorax
+BMGC_DS03068,BMG_DS004102,intestinal tuberculosis
+BMGC_DS03069,BMG_DS004107,Tuberculosis of urinary bladder
+BMGC_DS03070,BMG_DS004108,Tuberculosis of ureter
+BMGC_DS03071,BMG_DS004109,Tuberculosis of epididymis
+BMGC_DS03072,BMG_DS004111,Tuberculous oophoritis and salpingitis
+BMGC_DS03073,BMG_DS004114,Tuberculosis of ear
+BMGC_DS03074,BMG_DS004117,Tuberculosis of esophagus
+BMGC_DS03075,BMG_DS004120,Septicemic Plague
+BMGC_DS03076,BMG_DS004121,Primary pneumonic plague
+BMGC_DS03077,BMG_DS004122,Secondary pneumonic plague
+BMGC_DS03078,BMG_DS004123,Ulceroglandular tularemia
+BMGC_DS03079,BMG_DS004124,Enteric tularemia
+BMGC_DS03080,BMG_DS004125,Oculoglandular tularemia
+BMGC_DS03081,BMG_DS004126,Gastrointestinal anthrax
+BMGC_DS03082,BMG_DS004127,Anthrax sepsis
+BMGC_DS03083,BMG_DS004129,Diphtheritic myocarditis
+BMGC_DS03084,BMG_DS004130,Diphtheritic peritonitis
+BMGC_DS03085,BMG_DS004131,Diphtheritic cystitis
+BMGC_DS03086,BMG_DS004138,Streptococcal sepsis
+BMGC_DS03087,BMG_DS004140,Septicemia due to anaerobes
+BMGC_DS03088,BMG_DS004143,Acute nonparalytic poliomyelitis
+BMGC_DS03089,BMG_DS004153,Herpes zoster keratoconjunctivitis
+BMGC_DS03090,BMG_DS004158,Herpes simplex eyelid dermatitis
+BMGC_DS03091,BMG_DS004161,Herpetic whitlow
+BMGC_DS03092,BMG_DS004176,"Encephalomyelitis, Western Equine"
+BMGC_DS03093,BMG_DS004177,"Encephalomyelitis, Eastern Equine"
+BMGC_DS03094,BMG_DS004178,Murray valley encephalitis
+BMGC_DS03095,BMG_DS004201,"Trachoma, initial stage"
+BMGC_DS03096,BMG_DS004202,"Trachoma, active stage"
+BMGC_DS03097,BMG_DS004205,Acute Peripheral Vestibulopathy
+BMGC_DS03098,BMG_DS004211,Mixed malaria
+BMGC_DS03099,BMG_DS004217,"Neurosyphilis, Juvenile"
+BMGC_DS03100,BMG_DS004220,late congenital syphilis
+BMGC_DS03101,BMG_DS004221,Early symptomatic syphilis
+BMGC_DS03102,BMG_DS004238,Syphilitic aseptic meningitis
+BMGC_DS03103,BMG_DS004239,"Neurosyphilis, Asymptomatic"
+BMGC_DS03104,BMG_DS004240,Syphilitic encephalitis
+BMGC_DS03105,BMG_DS004255,"Syphilis, tertiary"
+BMGC_DS03106,BMG_DS004256,Acute gonococcal cystitis
+BMGC_DS03107,BMG_DS004257,Acute gonococcal prostatitis
+BMGC_DS03108,BMG_DS004258,Acute gonococcal epididymo-orchitis
+BMGC_DS03109,BMG_DS004260,Acute gonococcal cervicitis
+BMGC_DS03110,BMG_DS004261,Acute gonococcal endometritis
+BMGC_DS03111,BMG_DS004265,Chronic gonococcal seminal vesiculitis
+BMGC_DS03112,BMG_DS004266,Chronic gonococcal cervicitis
+BMGC_DS03113,BMG_DS004268,Chronic gonococcal salpingitis
+BMGC_DS03114,BMG_DS004270,Gonococcal iridocyclitis
+BMGC_DS03115,BMG_DS004271,Gonococcal endophthalmia
+BMGC_DS03116,BMG_DS004272,Gonococcal keratitis
+BMGC_DS03117,BMG_DS004274,Gonococcal joint infection
+BMGC_DS03118,BMG_DS004275,Gonococcal bursitis
+BMGC_DS03119,BMG_DS004276,Gonococcal spondylitis
+BMGC_DS03120,BMG_DS004279,Gonococcal meningitis
+BMGC_DS03121,BMG_DS004281,Gonococcal endocarditis
+BMGC_DS03122,BMG_DS004285,Multiple papillomata and wet crab yaws
+BMGC_DS03123,BMG_DS004288,Latent yaws
+BMGC_DS03124,BMG_DS004294,tinea manus
+BMGC_DS03125,BMG_DS004295,Black piedra
+BMGC_DS03126,BMG_DS004298,Systemic candidiasis
+BMGC_DS03127,BMG_DS004300,Candidal endocarditis
+BMGC_DS03128,BMG_DS004302,Candidal meningitis
+BMGC_DS03129,BMG_DS004303,Primary pulmonary coccidioidomycosis
+BMGC_DS03130,BMG_DS004305,Histoplasma capsulatum Infection
+BMGC_DS03131,BMG_DS004309,African histoplasmosis
+BMGC_DS03132,BMG_DS004314,histoplasmosis meningitis
+BMGC_DS03133,BMG_DS004315,Histoplasmosis with retinitis
+BMGC_DS03134,BMG_DS004316,Histoplasmosis with pericarditis
+BMGC_DS03135,BMG_DS004319,Echinococcus granulosus infection of liver
+BMGC_DS03136,BMG_DS004320,Echinococcus granulosus infection of lung
+BMGC_DS03137,BMG_DS004327,Mixed intestinal infection caused by Cestoda and/or Trematoda and/or Phylum Nemata
+BMGC_DS03138,BMG_DS004341,lip cancer
+BMGC_DS03139,BMG_DS004342,lip cancer
+BMGC_DS03140,BMG_DS004343,lip cancer
+BMGC_DS03141,BMG_DS004344,tongue cancer
+BMGC_DS03142,BMG_DS004345,tongue cancer
+BMGC_DS03143,BMG_DS004346,tongue cancer
+BMGC_DS03144,BMG_DS004347,tongue cancer
+BMGC_DS03145,BMG_DS004348,submandibular gland cancer
+BMGC_DS03146,BMG_DS004349,sublingual gland cancer
+BMGC_DS03147,BMG_DS004350,salivary gland cancer
+BMGC_DS03148,BMG_DS004351,gingival cancer
+BMGC_DS03149,BMG_DS004352,upper gum cancer
+BMGC_DS03150,BMG_DS004353,malignant tumor of floor of mouth
+BMGC_DS03151,BMG_DS004354,oral cavity cancer
+BMGC_DS03152,BMG_DS004355,cheek mucosa cancer
+BMGC_DS03153,BMG_DS004356,vestibule of mouth cancer
+BMGC_DS03154,BMG_DS004357,hard palate cancer
+BMGC_DS03155,BMG_DS004358,soft palate cancer
+BMGC_DS03156,BMG_DS004359,uvula cancer
+BMGC_DS03157,BMG_DS004360,retromolar area cancer
+BMGC_DS03158,BMG_DS004362,oropharynx cancer
+BMGC_DS03159,BMG_DS004363,tonsillar fossa cancer
+BMGC_DS03160,BMG_DS004364,tonsillar pillar cancer
+BMGC_DS03161,BMG_DS004365,vallecula cancer
+BMGC_DS03162,BMG_DS004366,oropharynx cancer
+BMGC_DS03163,BMG_DS004367,oropharynx cancer
+BMGC_DS03164,BMG_DS004368,oropharynx cancer
+BMGC_DS03165,BMG_DS004369,malignant tumor of nasopharynx
+BMGC_DS03166,BMG_DS004370,nasopharynx carcinoma
+BMGC_DS03167,BMG_DS004371,nasopharynx carcinoma
+BMGC_DS03168,BMG_DS004372,nasopharynx carcinoma
+BMGC_DS03169,BMG_DS004373,nasopharynx carcinoma
+BMGC_DS03170,BMG_DS004374,hypopharynx cancer
+BMGC_DS03171,BMG_DS004375,pyriform sinus cancer
+BMGC_DS03172,BMG_DS004376,aryepiglottic fold cancer
+BMGC_DS03173,BMG_DS004378,Waldeyer's ring cancer
+BMGC_DS03174,BMG_DS004380,esophageal cancer
+BMGC_DS03175,BMG_DS004381,esophageal cancer
+BMGC_DS03176,BMG_DS004382,esophageal cancer
+BMGC_DS03177,BMG_DS004383,esophageal cancer
+BMGC_DS03178,BMG_DS004384,cardia cancer
+BMGC_DS03179,BMG_DS004385,pylorus cancer
+BMGC_DS03180,BMG_DS004386,pyloric antrum cancer
+BMGC_DS03181,BMG_DS004387,gastric fundus cancer
+BMGC_DS03182,BMG_DS004388,stomach cancer
+BMGC_DS03183,BMG_DS004389,stomach cancer
+BMGC_DS03184,BMG_DS004390,stomach cancer
+BMGC_DS03185,BMG_DS004391,small intestine cancer
+BMGC_DS03186,BMG_DS004392,duodenum cancer
+BMGC_DS03187,BMG_DS004393,jejunal cancer
+BMGC_DS03188,BMG_DS004394,ileum cancer
+BMGC_DS03189,BMG_DS004395,Meckel diverticulum cancer
+BMGC_DS03190,BMG_DS004396,hepatic flexure cancer
+BMGC_DS03191,BMG_DS004397,transverse colon cancer
+BMGC_DS03192,BMG_DS004398,descending colon cancer
+BMGC_DS03193,BMG_DS004399,sigmoid colon cancer
+BMGC_DS03194,BMG_DS004400,cecum cancer
+BMGC_DS03195,BMG_DS004401,ascending colon cancer
+BMGC_DS03196,BMG_DS004402,splenic flexure cancer
+BMGC_DS03197,BMG_DS004403,rectosigmoid junction cancer
+BMGC_DS03198,BMG_DS004404,anal canal cancer
+BMGC_DS03199,BMG_DS004405,anus cancer
+BMGC_DS03200,BMG_DS004406,gallbladder cancer
+BMGC_DS03201,BMG_DS004407,malignant tumor of extrahepatic bile duct
+BMGC_DS03202,BMG_DS004408,ampulla of vater cancer
+BMGC_DS03203,BMG_DS004409,pancreatic cancer
+BMGC_DS03204,BMG_DS004410,pancreatic cancer
+BMGC_DS03205,BMG_DS004411,pancreatic cancer
+BMGC_DS03206,BMG_DS004412,pancreatic ductal carcinoma
+BMGC_DS03207,BMG_DS004413,pancreatic cancer
+BMGC_DS03208,BMG_DS004414,retroperitoneal cancer
+BMGC_DS03209,BMG_DS004415,retroperitoneal cancer
+BMGC_DS03210,BMG_DS004416,peritoneum cancer
+BMGC_DS03211,BMG_DS004417,peritoneum cancer
+BMGC_DS03212,BMG_DS004418,spleen cancer
+BMGC_DS03213,BMG_DS004420,maxillary sinus cancer
+BMGC_DS03214,BMG_DS004421,ethmoid sinus cancer
+BMGC_DS03215,BMG_DS004422,frontal sinus cancer
+BMGC_DS03216,BMG_DS004423,sphenoidal sinus cancer
+BMGC_DS03217,BMG_DS004424,glottis cancer
+BMGC_DS03218,BMG_DS004425,supraglottis cancer
+BMGC_DS03219,BMG_DS004426,subglottis cancer
+BMGC_DS03220,BMG_DS004427,laryngeal cartilage cancer
+BMGC_DS03221,BMG_DS004428,tracheal cancer
+BMGC_DS03222,BMG_DS004429,main bronchus cancer
+BMGC_DS03223,BMG_DS004430,lung cancer
+BMGC_DS03224,BMG_DS004431,lung cancer
+BMGC_DS03225,BMG_DS004432,lung cancer
+BMGC_DS03226,BMG_DS004433,pleural cancer
+BMGC_DS03227,BMG_DS004434,malignant parietal pleura tumor
+BMGC_DS03228,BMG_DS004435,malignant visceral pleura tumor
+BMGC_DS03229,BMG_DS004436,heart cancer
+BMGC_DS03230,BMG_DS004437,posterior mediastinum cancer
+BMGC_DS03231,BMG_DS004438,mediastinal cancer
+BMGC_DS03232,BMG_DS004439,mandibular cancer
+BMGC_DS03233,BMG_DS004440,long bones of lower limb cancer
+BMGC_DS03234,BMG_DS004441,cancer of short bone of lower limb
+BMGC_DS03235,BMG_DS004442,sarcoma
+BMGC_DS03236,BMG_DS004449,Kaposi's sarcoma
+BMGC_DS03237,BMG_DS004450,Kaposi's sarcoma
+BMGC_DS03238,BMG_DS004451,Kaposi's sarcoma
+BMGC_DS03239,BMG_DS004452,Kaposi's sarcoma
+BMGC_DS03240,BMG_DS004453,Kaposi's sarcoma
+BMGC_DS03241,BMG_DS004454,Kaposi's sarcoma
+BMGC_DS03242,BMG_DS004455,uterine cancer
+BMGC_DS03243,BMG_DS004457,placenta cancer
+BMGC_DS03244,BMG_DS004458,uterine corpus cancer
+BMGC_DS03245,BMG_DS004459,cancer of isthmus of fallopian tube
+BMGC_DS03246,BMG_DS004460,uterine adnexa cancer
+BMGC_DS03247,BMG_DS004461,fallopian tube cancer
+BMGC_DS03248,BMG_DS004462,parametrium malignant neoplasm
+BMGC_DS03249,BMG_DS004463,uterine adnexa cancer
+BMGC_DS03250,BMG_DS004464,female reproductive organ cancer
+BMGC_DS03251,BMG_DS004465,clitoris cancer
+BMGC_DS03252,BMG_DS004466,testicular cancer
+BMGC_DS03253,BMG_DS004467,malignant tumor of undescended testis
+BMGC_DS03254,BMG_DS004468,prepuce cancer
+BMGC_DS03255,BMG_DS004469,glans penis cancer
+BMGC_DS03256,BMG_DS004470,penile cancer
+BMGC_DS03257,BMG_DS004471,penile cancer
+BMGC_DS03258,BMG_DS004472,epididymis cancer
+BMGC_DS03259,BMG_DS004473,spermatic cord cancer
+BMGC_DS03260,BMG_DS004474,scrotum cancer
+BMGC_DS03261,BMG_DS004475,male reproductive organ cancer
+BMGC_DS03262,BMG_DS004476,urinary bladder anterior wall cancer
+BMGC_DS03263,BMG_DS004477,urinary bladder posterior wall cancer
+BMGC_DS03264,BMG_DS004478,bladder neck cancer
+BMGC_DS03265,BMG_DS004479,ureteric orifice cancer
+BMGC_DS03266,BMG_DS004480,urachus cancer
+BMGC_DS03267,BMG_DS004481,malignant renal pelvis neoplasm
+BMGC_DS03268,BMG_DS004482,ureter cancer
+BMGC_DS03269,BMG_DS004483,urethra cancer
+BMGC_DS03270,BMG_DS004484,paraurethral gland cancer
+BMGC_DS03271,BMG_DS004485,orbital cancer
+BMGC_DS03272,BMG_DS004486,lacrimal gland cancer
+BMGC_DS03273,BMG_DS004487,conjunctival cancer
+BMGC_DS03274,BMG_DS004488,cornea cancer
+BMGC_DS03275,BMG_DS004489,choroid cancer
+BMGC_DS03276,BMG_DS004490,lacrimal duct cancer
+BMGC_DS03277,BMG_DS004491,ocular cancer
+BMGC_DS03278,BMG_DS004492,brain cancer
+BMGC_DS03279,BMG_DS004493,frontal lobe neoplasm
+BMGC_DS03280,BMG_DS004494,temporal lobe cancer
+BMGC_DS03281,BMG_DS004495,parietal lobe cancer
+BMGC_DS03282,BMG_DS004496,occipital lobe neoplasm
+BMGC_DS03283,BMG_DS004497,cancer of cerebellum
+BMGC_DS03284,BMG_DS004498,brainstem cancer
+BMGC_DS03285,BMG_DS004499,cerebrum cancer
+BMGC_DS03286,BMG_DS004500,nervous system cancer
+BMGC_DS03287,BMG_DS004501,malignant cranial nerve neoplasm
+BMGC_DS03288,BMG_DS004502,spinal cord cancer
+BMGC_DS03289,BMG_DS004503,spinal meninges cancer
+BMGC_DS03290,BMG_DS004504,malignant tumor of parathyroid gland
+BMGC_DS03291,BMG_DS004505,pineal gland cancer
+BMGC_DS03292,BMG_DS004506,malignant carotid body paraganglioma
+BMGC_DS03293,BMG_DS004507,malignant endocrine neoplasm
+BMGC_DS03294,BMG_DS004508,thoracic cancer
+BMGC_DS03295,BMG_DS004510,intrapelvic lymph node leukemic reticuloendotheliosis
+BMGC_DS03296,BMG_DS004511,splenic manifestation of hairy cell leukemia
+BMGC_DS03297,BMG_DS004512,intra-abdominal lymph node mast cell malignancy
+BMGC_DS03298,BMG_DS004513,monocytic leukemia
+BMGC_DS03299,BMG_DS004514,subacute leukemia
+BMGC_DS03300,BMG_DS004530,lipoma of face
+BMGC_DS03301,BMG_DS004531,lipoma of spermatic cord
+BMGC_DS03302,BMG_DS004532,submucous uterine fibroid
+BMGC_DS03303,BMG_DS004533,uterus interstitial leiomyoma
+BMGC_DS03304,BMG_DS004534,subserous uterine fibroid
+BMGC_DS03305,BMG_DS004535,cervical polyp
+BMGC_DS03306,BMG_DS004558,intracranial hemangioma
+BMGC_DS03307,BMG_DS004560,intra-abdominal hemangioma
+BMGC_DS03308,BMG_DS004563,esophagus carcinoma in situ
+BMGC_DS03309,BMG_DS004564,stomach carcinoma in situ
+BMGC_DS03310,BMG_DS004565,colon carcinoma in situ
+BMGC_DS03311,BMG_DS004566,rectum carcinoma in situ
+BMGC_DS03312,BMG_DS004567,anal carcinoma in situ
+BMGC_DS03313,BMG_DS004568,intestine carcinoma in situ
+BMGC_DS03314,BMG_DS004569,larynx carcinoma in situ
+BMGC_DS03315,BMG_DS004570,trachea carcinoma in situ
+BMGC_DS03316,BMG_DS004571,lung carcinoma in situ
+BMGC_DS03317,BMG_DS004572,skin carcinoma in situ
+BMGC_DS03318,BMG_DS004573,skin carcinoma in situ
+BMGC_DS03319,BMG_DS004574,skin carcinoma in situ
+BMGC_DS03320,BMG_DS004575,skin carcinoma in situ
+BMGC_DS03321,BMG_DS004576,skin carcinoma in situ
+BMGC_DS03322,BMG_DS004577,skin carcinoma in situ
+BMGC_DS03323,BMG_DS004578,skin carcinoma in situ
+BMGC_DS03324,BMG_DS004579,breast carcinoma in situ
+BMGC_DS03325,BMG_DS004580,uterus carcinoma in situ
+BMGC_DS03326,BMG_DS004581,prostate carcinoma in situ
+BMGC_DS03327,BMG_DS004582,penis carcinoma in situ
+BMGC_DS03328,BMG_DS004583,bladder carcinoma in situ
+BMGC_DS03329,BMG_DS004584,kidney carcinoma in situ
+BMGC_DS03330,BMG_DS004585,eye carcinoma in situ
+BMGC_DS03331,BMG_DS004586,toxic diffuse goiter
+BMGC_DS03332,BMG_DS004591,Postoperative hypothyroidism
+BMGC_DS03333,BMG_DS004593,Iodine hypothyroidism
+BMGC_DS03334,BMG_DS004595,Riedel's thyroiditis
+BMGC_DS03335,BMG_DS004599,Other disorders of pancreatic internal secretion
+BMGC_DS03336,BMG_DS004600,Post-surgical hypoinsulinemia
+BMGC_DS03337,BMG_DS004601,Abnormality of secretion of glucagon
+BMGC_DS03338,BMG_DS004605,Disease of thymus gland
+BMGC_DS03339,BMG_DS004608,Medulloadrenal hyperfunction
+BMGC_DS03340,BMG_DS004611,Hyperestrogenism
+BMGC_DS03341,BMG_DS004619,Polyglandular dysfunction
+BMGC_DS03342,BMG_DS004632,"Urea Cycle Disorders, Inborn"
+BMGC_DS03343,BMG_DS004633,Lipid Metabolism Disorders
+BMGC_DS03344,BMG_DS004634,Polyclonal hypergammaglobulinemia
+BMGC_DS03345,BMG_DS004640,B cell deficiency
+BMGC_DS03346,BMG_DS004646,Anemia due to protein deficiency
+BMGC_DS03347,BMG_DS004650,Acquired thrombocytopenia
+BMGC_DS03348,BMG_DS004651,Chronic lymphadenitis
+BMGC_DS03349,BMG_DS004654,dementia
+BMGC_DS03350,BMG_DS004655,drug-induced mental disorder
+BMGC_DS03351,BMG_DS004657,subacute delirium
+BMGC_DS03352,BMG_DS004658,substance-induced psychosis
+BMGC_DS03353,BMG_DS004659,major depressive disorder
+BMGC_DS03354,BMG_DS004660,atypical depressive disorder
+BMGC_DS03355,BMG_DS004661,pervasive developmental disorder
+BMGC_DS03356,BMG_DS004662,psychologic dyspareunia
+BMGC_DS03357,BMG_DS004663,barbiturate dependence
+BMGC_DS03358,BMG_DS004664,barbiturate abuse
+BMGC_DS03359,BMG_DS004665,amphetamine abuse
+BMGC_DS03360,BMG_DS004666,antidepressant type abuse
+BMGC_DS03361,BMG_DS004669,sleep disorder
+BMGC_DS03362,BMG_DS004670,rumination disorder
+BMGC_DS03363,BMG_DS004671,reading disorder
+BMGC_DS03364,BMG_DS004672,Streptococcal meningitis
+BMGC_DS03365,BMG_DS004673,Staphylococcal meningitis
+BMGC_DS03366,BMG_DS004675,Sarcoid meningitis
+BMGC_DS03367,BMG_DS004677,Eosinophilic meningitis
+BMGC_DS03368,BMG_DS004678,Chronic meningitis
+BMGC_DS03369,BMG_DS004683,Senile degeneration of brain
+BMGC_DS03370,BMG_DS004684,Degenerative brain disorder
+BMGC_DS03371,BMG_DS004685,Symptomatic torsion dystonia
+BMGC_DS03372,BMG_DS004686,Fragments of torsion dystonia
+BMGC_DS03373,BMG_DS004688,Anterior Horn Cell Disease
+BMGC_DS03374,BMG_DS004689,Lateral Sclerosis
+BMGC_DS03375,BMG_DS004690,Vascular myelopathy
+BMGC_DS03376,BMG_DS004693,Idiopathic peripheral autonomic neuropathy
+BMGC_DS03377,BMG_DS004694,autonomic nervous system disease
+BMGC_DS03378,BMG_DS004696,"Hemiplegia, Flaccid"
+BMGC_DS03379,BMG_DS004697,"Hemiplegia, Spastic"
+BMGC_DS03380,BMG_DS004698,Diplegic Infantile Cerebral Palsy
+BMGC_DS03381,BMG_DS004699,"Cerebral Palsy, Quadriplegic, Infantile"
+BMGC_DS03382,BMG_DS004700,Monoplegic Infantile Cerebral Palsy
+BMGC_DS03383,BMG_DS004702,Diplegia of upper limbs
+BMGC_DS03384,BMG_DS004706,simple partial epilepsy
+BMGC_DS03385,BMG_DS004707,Migraine with Aura
+BMGC_DS03386,BMG_DS004711,Disorders of other cranial nerves
+BMGC_DS03387,BMG_DS004712,Glossopharyngeal Neuralgia
+BMGC_DS03388,BMG_DS004713,Multiple cranial nerve palsy
+BMGC_DS03389,BMG_DS004714,Lumbosacral plexus lesion
+BMGC_DS03390,BMG_DS004718,Mononeuritis of upper limb and mononeuritis multiplex
+BMGC_DS03391,BMG_DS004719,median neuropathy
+BMGC_DS03392,BMG_DS004720,Ulnar Neuropathies
+BMGC_DS03393,BMG_DS004721,Lesion of radial nerve
+BMGC_DS03394,BMG_DS004722,mononeuritis of upper limb
+BMGC_DS03395,BMG_DS004723,Mononeuritis of lower limb
+BMGC_DS03396,BMG_DS004724,Lesion of Sciatic Nerve
+BMGC_DS03397,BMG_DS004725,Tibial nerve palsy
+BMGC_DS03398,BMG_DS004726,Plantar nerve lesion
+BMGC_DS03399,BMG_DS004728,Idiopathic progressive polyneuropathy
+BMGC_DS03400,BMG_DS004729,inflammatory and toxic neuropathy
+BMGC_DS03401,BMG_DS004730,Polyneuropathy in collagen vascular disease
+BMGC_DS03402,BMG_DS004731,Polyneuropathy caused by drug
+BMGC_DS03403,BMG_DS004735,Acute endophthalmitis
+BMGC_DS03404,BMG_DS004736,Chronic endophthalmitis
+BMGC_DS03405,BMG_DS004737,Ophthalmia nodosa
+BMGC_DS03406,BMG_DS004738,Degenerative disorder of eye
+BMGC_DS03407,BMG_DS004739,"Myopia, Degenerative"
+BMGC_DS03408,BMG_DS004740,Other degenerative disorders of globe
+BMGC_DS03409,BMG_DS004741,Primary hypotony of eye
+BMGC_DS03410,BMG_DS004742,Blind hypotensive eye
+BMGC_DS03411,BMG_DS004743,Blind hypertensive eye
+BMGC_DS03412,BMG_DS004745,Luxation of eye
+BMGC_DS03413,BMG_DS004748,Flat retinoschisis
+BMGC_DS03414,BMG_DS004756,Proliferative diabetic retinopathy
+BMGC_DS03415,BMG_DS004757,Exudative retinopathy
+BMGC_DS03416,BMG_DS004758,retinal vascular disorder
+BMGC_DS03417,BMG_DS004759,retinal microaneurysm
+BMGC_DS03418,BMG_DS004760,Retinal telangiectasia
+BMGC_DS03419,BMG_DS004763,Partial retinal artery occlusion
+BMGC_DS03420,BMG_DS004764,Transient arterial retinal occlusion
+BMGC_DS03421,BMG_DS004765,Central retinal vein occlusion
+BMGC_DS03422,BMG_DS004766,venous tributary occlusion of retina
+BMGC_DS03423,BMG_DS004768,Cystoid macular retinal degeneration
+BMGC_DS03424,BMG_DS004769,Paving stone retinal degeneration
+BMGC_DS03425,BMG_DS004770,Microcystoid retinal degeneration
+BMGC_DS03426,BMG_DS004771,Retinal lattice degeneration
+BMGC_DS03427,BMG_DS004772,Senile reticular retinal degeneration
+BMGC_DS03428,BMG_DS004773,Secondary pigmentary retinal degeneration
+BMGC_DS03429,BMG_DS004774,Secondary vitreoretinal degeneration
+BMGC_DS03430,BMG_DS004775,Hereditary retinal dystrophy
+BMGC_DS03431,BMG_DS004776,retinal dystrophy in systemic or cerebroretinal lipidoses
+BMGC_DS03432,BMG_DS004777,Vitreoretinal dystrophy
+BMGC_DS03433,BMG_DS004779,Dystrophies primarily involving the retinal pigment epithelium
+BMGC_DS03434,BMG_DS004780,retinal dystrophies primarily involving Bruch's membrane
+BMGC_DS03435,BMG_DS004781,Focal chorioretinitis
+BMGC_DS03436,BMG_DS004784,Neuroretinitis
+BMGC_DS03437,BMG_DS004787,Disseminated chorioretinitis
+BMGC_DS03438,BMG_DS004793,peripheral scars of retina
+BMGC_DS03439,BMG_DS004794,Senile atrophy of choroid
+BMGC_DS03440,BMG_DS004795,Diffuse secondary choroid atrophy
+BMGC_DS03441,BMG_DS004796,Hereditary choroidal dystrophy
+BMGC_DS03442,BMG_DS004797,Partial circumpapillary choroid dystrophy
+BMGC_DS03443,BMG_DS004798,Total circumpapillary dystrophy of choroid
+BMGC_DS03444,BMG_DS004799,total central choroidal atrophy
+BMGC_DS03445,BMG_DS004805,Disorder of iris and ciliary body
+BMGC_DS03446,BMG_DS004807,Primary iridocyclitis
+BMGC_DS03447,BMG_DS004809,Secondary infected iridocyclitis
+BMGC_DS03448,BMG_DS004812,Rubeosis iridis
+BMGC_DS03449,BMG_DS004824,anatomical narrow angle borderline glaucoma
+BMGC_DS03450,BMG_DS004825,Residual stage of open angle glaucoma
+BMGC_DS03451,BMG_DS004826,Intermittent angle-closure glaucoma
+BMGC_DS03452,BMG_DS004827,Acute angle-closure glaucoma
+BMGC_DS03453,BMG_DS004828,Anatomical narrow angle glaucoma
+BMGC_DS03454,BMG_DS004829,Residual stage of angle-closure glaucoma
+BMGC_DS03455,BMG_DS004834,phacogenic glaucoma
+BMGC_DS03456,BMG_DS004839,Hypersecretion glaucoma
+BMGC_DS03457,BMG_DS004843,Cortical senile cataract
+BMGC_DS03458,BMG_DS004847,Transient refractive change
+BMGC_DS03459,BMG_DS004851,Abnormal retinal correspondence
+BMGC_DS03460,BMG_DS004852,"Color Blindness, Red"
+BMGC_DS03461,BMG_DS004853,"Color Blindness, Red-Green"
+BMGC_DS03462,BMG_DS004854,"Color Blindness, Blue"
+BMGC_DS03463,BMG_DS004855,"Color Blindness, Acquired"
+BMGC_DS03464,BMG_DS004856,Abnormal dark adaptation curve
+BMGC_DS03465,BMG_DS004857,blindness
+BMGC_DS03466,BMG_DS004858,Marginal corneal ulcer
+BMGC_DS03467,BMG_DS004859,Ring corneal ulcer
+BMGC_DS03468,BMG_DS004860,Central corneal ulcer
+BMGC_DS03469,BMG_DS004861,Hypopyon ulcer
+BMGC_DS03470,BMG_DS004862,Mycotic corneal ulcer
+BMGC_DS03471,BMG_DS004863,Mooren's ulcer
+BMGC_DS03472,BMG_DS004864,Superficial keratitis
+BMGC_DS03473,BMG_DS004865,Macular keratitis
+BMGC_DS03474,BMG_DS004866,Filamentary keratitis
+BMGC_DS03475,BMG_DS004867,Photokeratitis
+BMGC_DS03476,BMG_DS004868,Phlyctenular keratoconjunctivitis
+BMGC_DS03477,BMG_DS004870,Neurotrophic keratoconjunctivitis
+BMGC_DS03478,BMG_DS004871,Interstitial and deep keratitis
+BMGC_DS03479,BMG_DS004872,Interstitial keratitis
+BMGC_DS03480,BMG_DS004873,Diffuse interstitial keratitis
+BMGC_DS03481,BMG_DS004874,Sclerosing keratitis
+BMGC_DS03482,BMG_DS004875,Corneal abscess
+BMGC_DS03483,BMG_DS004879,Deep vascularization of cornea
+BMGC_DS03484,BMG_DS004881,Phthisical cornea
+BMGC_DS03485,BMG_DS004882,Anterior corneal pigmentation
+BMGC_DS03486,BMG_DS004883,Stromal corneal pigmentation
+BMGC_DS03487,BMG_DS004884,Posterior corneal pigmentation
+BMGC_DS03488,BMG_DS004885,Argentous corneal deposit
+BMGC_DS03489,BMG_DS004886,Idiopathic corneal edema
+BMGC_DS03490,BMG_DS004887,Secondary corneal edema
+BMGC_DS03491,BMG_DS004888,Bullous keratopathy
+BMGC_DS03492,BMG_DS004889,Folds AND/OR rupture of Bowman's membrane
+BMGC_DS03493,BMG_DS004890,Corneal degeneration
+BMGC_DS03494,BMG_DS004891,Recurrent erosion of cornea
+BMGC_DS03495,BMG_DS004892,"Corneal Dystrophy, Band-Shaped"
+BMGC_DS03496,BMG_DS004894,Nodular degeneration of cornea
+BMGC_DS03497,BMG_DS004895,Peripheral degeneration of cornea
+BMGC_DS03498,BMG_DS004897,"Familial Amyloid Polyneuropathy, Type V"
+BMGC_DS03499,BMG_DS004898,"Keratoconus, stable condition"
+BMGC_DS03500,BMG_DS004899,Corneal ectasia
+BMGC_DS03501,BMG_DS004901,"Serous conjunctivitis, except viral"
+BMGC_DS03502,BMG_DS004902,Acute follicular conjunctivitis
+BMGC_DS03503,BMG_DS004903,Pseudomembranous conjunctivitis
+BMGC_DS03504,BMG_DS004904,Chronic conjunctivitis
+BMGC_DS03505,BMG_DS004905,Simple chronic conjunctivitis
+BMGC_DS03506,BMG_DS004906,Chronic follicular conjunctivitis
+BMGC_DS03507,BMG_DS004907,Parasitic conjunctivitis
+BMGC_DS03508,BMG_DS004908,Angular blepharoconjunctivitis
+BMGC_DS03509,BMG_DS004909,Contact blepharoconjunctivitis
+BMGC_DS03510,BMG_DS004910,Rosacea conjunctivitis
+BMGC_DS03511,BMG_DS004913,"Peripheral pterygium, progressive"
+BMGC_DS03512,BMG_DS004914,central pterygium
+BMGC_DS03513,BMG_DS004915,Double pterygium
+BMGC_DS03514,BMG_DS004917,Conjunctival degeneration
+BMGC_DS03515,BMG_DS004918,Pseudopterygium
+BMGC_DS03516,BMG_DS004919,conjunctival concretion
+BMGC_DS03517,BMG_DS004920,Conjunctival pigmentation
+BMGC_DS03518,BMG_DS004924,Ocular hyperemia
+BMGC_DS03519,BMG_DS004927,Ulcerative blepharitis
+BMGC_DS03520,BMG_DS004928,Squamous blepharitis
+BMGC_DS03521,BMG_DS004930,Noninfectious dermatosis of eyelid
+BMGC_DS03522,BMG_DS004931,Eczematous dermatitis of eyelid
+BMGC_DS03523,BMG_DS004932,Allergic contact dermatitis of eyelid
+BMGC_DS03524,BMG_DS004933,Xeroderma of eyelid
+BMGC_DS03525,BMG_DS004934,Discoid lupus erythematosus of eyelid
+BMGC_DS03526,BMG_DS004935,blepharitis
+BMGC_DS03527,BMG_DS004936,Parasitic eyelid infestation
+BMGC_DS03528,BMG_DS004938,Senile entropion
+BMGC_DS03529,BMG_DS004939,Mechanical entropion
+BMGC_DS03530,BMG_DS004940,Spastic entropion
+BMGC_DS03531,BMG_DS004941,Cicatricial entropion
+BMGC_DS03532,BMG_DS004942,Senile ectropion
+BMGC_DS03533,BMG_DS004943,Mechanical ectropion
+BMGC_DS03534,BMG_DS004944,Spastic ectropion
+BMGC_DS03535,BMG_DS004945,Cicatricial ectropion
+BMGC_DS03536,BMG_DS004946,Paralytic Lagophthalmos
+BMGC_DS03537,BMG_DS004947,Mechanical lagophthalmos
+BMGC_DS03538,BMG_DS004948,Cicatricial Lagophthalmos
+BMGC_DS03539,BMG_DS004952,Hyperpigmentation of Eyelids
+BMGC_DS03540,BMG_DS004953,Hypopigmentation of eyelid
+BMGC_DS03541,BMG_DS004954,Hypertrichosis of eyelid
+BMGC_DS03542,BMG_DS004955,Hypotrichosis of eyelid
+BMGC_DS03543,BMG_DS004958,Dacryoadenitis
+BMGC_DS03544,BMG_DS004959,Chronic dacryoadenitis
+BMGC_DS03545,BMG_DS004961,Primary lacrimal atrophy
+BMGC_DS03546,BMG_DS004962,Dislocation of lacrimal gland
+BMGC_DS03547,BMG_DS004963,Epiphora due to excess lacrimation
+BMGC_DS03548,BMG_DS004964,Epiphora due to insufficient drainage
+BMGC_DS03549,BMG_DS004965,Acute dacryocystitis
+BMGC_DS03550,BMG_DS004966,Phlegmonous dacryocystitis
+BMGC_DS03551,BMG_DS004967,Chronic inflammation of lacrimal passage
+BMGC_DS03552,BMG_DS004968,Chronic lacrimal canaliculitis
+BMGC_DS03553,BMG_DS004969,Lacrimal mucocele
+BMGC_DS03554,BMG_DS004970,Eversion of lacrimal punctum
+BMGC_DS03555,BMG_DS004971,Stenosis of lacrimal punctum
+BMGC_DS03556,BMG_DS004972,stenosis of lacrimal passage
+BMGC_DS03557,BMG_DS004973,stenosis of lacrimal sac
+BMGC_DS03558,BMG_DS004975,acquired tear duct stenosis
+BMGC_DS03559,BMG_DS004978,Lacrimal passage granuloma
+BMGC_DS03560,BMG_DS004979,acute orbital inflammation
+BMGC_DS03561,BMG_DS004980,Orbital periostitis
+BMGC_DS03562,BMG_DS004981,Orbital osteomyelitis
+BMGC_DS03563,BMG_DS004982,Tenonitis
+BMGC_DS03564,BMG_DS004983,Chronic inflammation of orbit
+BMGC_DS03565,BMG_DS004984,Orbital granuloma
+BMGC_DS03566,BMG_DS004986,Endocrine exophthalmos
+BMGC_DS03567,BMG_DS004987,Thyrotoxic exophthalmos
+BMGC_DS03568,BMG_DS004989,Constant exophthalmos
+BMGC_DS03569,BMG_DS004990,Intermittent exophthalmos
+BMGC_DS03570,BMG_DS004991,Pulsating exophthalmos
+BMGC_DS03571,BMG_DS004992,Lateral displacement of eye
+BMGC_DS03572,BMG_DS004997,Orbital cyst
+BMGC_DS03573,BMG_DS004998,Myopathy of extraocular muscles
+BMGC_DS03574,BMG_DS004999,Disorder of visual pathways
+BMGC_DS03575,BMG_DS005000,Papilledema Associated with Increased Intracranial Pressure
+BMGC_DS03576,BMG_DS005002,Primary optic atrophy
+BMGC_DS03577,BMG_DS005005,Partial optic atrophy
+BMGC_DS03578,BMG_DS005007,Crater-like holes of optic disc
+BMGC_DS03579,BMG_DS005008,coloboma of optic nerve
+BMGC_DS03580,BMG_DS005009,Pseudopapilledema
+BMGC_DS03581,BMG_DS005010,Acute retrobulbar neuritis
+BMGC_DS03582,BMG_DS005011,Nutritional optic neuropathy
+BMGC_DS03583,BMG_DS005012,Toxic Optic Neuropathy
+BMGC_DS03584,BMG_DS005013,"Optic Neuropathy, Ischemic"
+BMGC_DS03585,BMG_DS005014,Optic chiasm disorder
+BMGC_DS03586,BMG_DS005021,"Blindness, Cortical"
+BMGC_DS03587,BMG_DS005035,Esotropia with accommodative compensation
+BMGC_DS03588,BMG_DS005036,Total ophthalmoplegia
+BMGC_DS03589,BMG_DS005037,Brown Tendon Sheath Syndrome
+BMGC_DS03590,BMG_DS005039,Episcleritis periodica fugax
+BMGC_DS03591,BMG_DS005040,Nodular episcleritis
+BMGC_DS03592,BMG_DS005041,Anterior scleritis
+BMGC_DS03593,BMG_DS005042,Scleromalacia perforans
+BMGC_DS03594,BMG_DS005043,Scleritis with corneal involvement
+BMGC_DS03595,BMG_DS005044,Brawny scleritis
+BMGC_DS03596,BMG_DS005045,Posterior scleritis
+BMGC_DS03597,BMG_DS005047,Scleral staphyloma
+BMGC_DS03598,BMG_DS005048,Staphyloma posticum
+BMGC_DS03599,BMG_DS005049,Equatorial staphyloma
+BMGC_DS03600,BMG_DS005050,Localized anterior staphyloma
+BMGC_DS03601,BMG_DS005051,Ring staphyloma
+BMGC_DS03602,BMG_DS005053,Vitreous degeneration
+BMGC_DS03603,BMG_DS005057,Anterior dislocation of lens
+BMGC_DS03604,BMG_DS005058,Posterior dislocation of lens
+BMGC_DS03605,BMG_DS005059,Atypical Argyll-Robertson pupil (disorder)
+BMGC_DS03606,BMG_DS005060,Other anomalies of pupillary function
+BMGC_DS03607,BMG_DS005061,Nystagmus associated with disorder of the vestibular system
+BMGC_DS03608,BMG_DS005062,Dissociated Nystagmus
+BMGC_DS03609,BMG_DS005064,external ear disorder
+BMGC_DS03610,BMG_DS005065,Perichondritis of pinna
+BMGC_DS03611,BMG_DS005066,Acute perichondritis of pinna
+BMGC_DS03612,BMG_DS005067,Chronic perichondritis of pinna
+BMGC_DS03613,BMG_DS005068,Acute infection of pinna
+BMGC_DS03614,BMG_DS005069,Malignant otitis externa
+BMGC_DS03615,BMG_DS005070,Chronic mycotic otitis externa
+BMGC_DS03616,BMG_DS005072,Cholesteatoma of external ear
+BMGC_DS03617,BMG_DS005075,Exostosis of external ear canal
+BMGC_DS03618,BMG_DS005077,Acute serous otitis media
+BMGC_DS03619,BMG_DS005078,Acute allergic serous otitis media
+BMGC_DS03620,BMG_DS005079,Acute allergic mucoid otitis media
+BMGC_DS03621,BMG_DS005080,Acute allergic sanguineous otitis media
+BMGC_DS03622,BMG_DS005081,Chronic serous otitis media
+BMGC_DS03623,BMG_DS005082,Eustachian tube salpingitis
+BMGC_DS03624,BMG_DS005083,Acute eustachian tube salpingitis
+BMGC_DS03625,BMG_DS005084,Chronic eustachian tube salpingitis
+BMGC_DS03626,BMG_DS005087,Patulous eustachian tube
+BMGC_DS03627,BMG_DS005088,eustachian tube disease
+BMGC_DS03628,BMG_DS005089,purulent acute otitis media
+BMGC_DS03629,BMG_DS005090,Chronic tubotympanic suppurative otitis media
+BMGC_DS03630,BMG_DS005091,Chronic atticoantral suppurative otitis media
+BMGC_DS03631,BMG_DS005095,Petrositis
+BMGC_DS03632,BMG_DS005096,Acute petrositis
+BMGC_DS03633,BMG_DS005097,Chronic petrositis
+BMGC_DS03634,BMG_DS005100,Acute myringitis
+BMGC_DS03635,BMG_DS005101,Bullous myringitis
+BMGC_DS03636,BMG_DS005106,Atrophic flaccid tympanic membrane
+BMGC_DS03637,BMG_DS005107,Atrophic nonflaccid tympanic membrane
+BMGC_DS03638,BMG_DS005109,Tympanosclerosis involving other combination of structures
+BMGC_DS03639,BMG_DS005110,Adhesive middle ear disease
+BMGC_DS03640,BMG_DS005112,dislocation of ear ossicle
+BMGC_DS03641,BMG_DS005113,necrosis of ear ossicle
+BMGC_DS03642,BMG_DS005114,Cholesteatoma of attic
+BMGC_DS03643,BMG_DS005115,Middle Ear Cholesteatoma
+BMGC_DS03644,BMG_DS005117,middle ear cholesterol granuloma
+BMGC_DS03645,BMG_DS005119,Active cochleovestibular Ménière's disease
+BMGC_DS03646,BMG_DS005120,Active cochlear Ménière's disease
+BMGC_DS03647,BMG_DS005121,Active vestibular Ménière's disease
+BMGC_DS03648,BMG_DS005123,"Vertigo, Peripheral"
+BMGC_DS03649,BMG_DS005124,Benign Paroxysmal Positional Vertigo
+BMGC_DS03650,BMG_DS005125,Central Nervous System Origin Vertigo
+BMGC_DS03651,BMG_DS005126,Serous labyrinthitis
+BMGC_DS03652,BMG_DS005127,Circumscribed labyrinthitis
+BMGC_DS03653,BMG_DS005128,Suppurative labyrinthitis
+BMGC_DS03654,BMG_DS005129,Toxic labyrinthitis
+BMGC_DS03655,BMG_DS005130,Viral labyrinthitis
+BMGC_DS03656,BMG_DS005131,Labyrinthine dysfunction
+BMGC_DS03657,BMG_DS005132,unilateral hyperactive labyrinth
+BMGC_DS03658,BMG_DS005133,Hyperactive bilateral labyrinthine dysfunction
+BMGC_DS03659,BMG_DS005134,unilateral hypoactive labyrinth
+BMGC_DS03660,BMG_DS005135,Hypoactive bilateral labyrinthine dysfunction
+BMGC_DS03661,BMG_DS005136,labyrinthine unilateral reactive loss
+BMGC_DS03662,BMG_DS005137,labyrinthine bilateral reactive loss
+BMGC_DS03663,BMG_DS005142,discharging ear
+BMGC_DS03664,BMG_DS005154,Chronic rheumatic pericarditis
+BMGC_DS03665,BMG_DS005155,Rheumatic mitral regurgitation
+BMGC_DS03666,BMG_DS005156,Rheumatic aortic stenosis
+BMGC_DS03667,BMG_DS005157,Rheumatic aortic regurgitation
+BMGC_DS03668,BMG_DS005159,Rheumatic disease of pulmonary valve
+BMGC_DS03669,BMG_DS005160,Congestive rheumatic heart failure
+BMGC_DS03670,BMG_DS005161,Benign essential hypertension (disorder)
+BMGC_DS03671,BMG_DS005167,Malignant hypertensive renal disease
+BMGC_DS03672,BMG_DS005168,Benign hypertensive renal disease
+BMGC_DS03673,BMG_DS005173,Secondary hypertension
+BMGC_DS03674,BMG_DS005174,Malignant secondary hypertension
+BMGC_DS03675,BMG_DS005175,Benign secondary hypertension
+BMGC_DS03676,BMG_DS005176,benign renovascular hypertension
+BMGC_DS03677,BMG_DS005177,Acute myocardial infarction
+BMGC_DS03678,BMG_DS005178,Acute myocardial infarction of anterolateral wall
+BMGC_DS03679,BMG_DS005179,acute inferolateral myocardial infarction
+BMGC_DS03680,BMG_DS005180,acute inferoposterior infarction
+BMGC_DS03681,BMG_DS005181,strictly posterior acute myocardial infarction
+BMGC_DS03682,BMG_DS005182,subendocardial infarction acute myocardial infarction
+BMGC_DS03683,BMG_DS005184,Acute pulmonary heart disease
+BMGC_DS03684,BMG_DS005185,chronic pulmonary heart disease
+BMGC_DS03685,BMG_DS005187,Acute pericarditis
+BMGC_DS03686,BMG_DS005191,Acute myocarditis
+BMGC_DS03687,BMG_DS005192,Isolated (Fiedler's) myocarditis
+BMGC_DS03688,BMG_DS005193,Septic myocarditis
+BMGC_DS03689,BMG_DS005194,Toxic myocarditis
+BMGC_DS03690,BMG_DS005198,extrinsic cardiomyopathy
+BMGC_DS03691,BMG_DS005199,Mobitz type II atrioventricular block
+BMGC_DS03692,BMG_DS005200,Left bundle branch hemiblock
+BMGC_DS03693,BMG_DS005201,Right bundle branch block AND left posterior fascicular block
+BMGC_DS03694,BMG_DS005205,vertebral artery occlusion
+BMGC_DS03695,BMG_DS005206,Occlusion and stenosis of unspecified precerebral artery
+BMGC_DS03696,BMG_DS005208,Atherosclerosis of aorta
+BMGC_DS03697,BMG_DS005209,Atherosclerosis of renal artery
+BMGC_DS03698,BMG_DS005219,Disease of capillaries
+BMGC_DS03699,BMG_DS005221,Phlebitis and thrombophlebitis of iliac vein
+BMGC_DS03700,BMG_DS005222,portal vein thrombosis
+BMGC_DS03701,BMG_DS005223,vein disease
+BMGC_DS03702,BMG_DS005228,perianal hematoma
+BMGC_DS03703,BMG_DS005230,Bleeding esophageal varices
+BMGC_DS03704,BMG_DS005231,esophageal varix
+BMGC_DS03705,BMG_DS005232,esophageal varix
+BMGC_DS03706,BMG_DS005233,Varicose veins of pelvis
+BMGC_DS03707,BMG_DS005236,Acute maxillary sinusitis
+BMGC_DS03708,BMG_DS005237,Acute frontal sinusitis
+BMGC_DS03709,BMG_DS005238,Acute ethmoidal sinusitis
+BMGC_DS03710,BMG_DS005239,Acute sphenoidal sinusitis
+BMGC_DS03711,BMG_DS005242,Acute laryngitis and/or tracheitis
+BMGC_DS03712,BMG_DS005244,Acute epiglottitis
+BMGC_DS03713,BMG_DS005246,Acute laryngopharyngitis
+BMGC_DS03714,BMG_DS005250,Chronic pharyngitis and nasopharyngitis
+BMGC_DS03715,BMG_DS005252,Chronic nasopharyngitis
+BMGC_DS03716,BMG_DS005259,Chronic laryngitis
+BMGC_DS03717,BMG_DS005260,Chronic laryngotracheitis
+BMGC_DS03718,BMG_DS005272,Pneumonia caused by Pseudomonas
+BMGC_DS03719,BMG_DS005273,Streptococcal pneumonia
+BMGC_DS03720,BMG_DS005275,Inhalational anthrax
+BMGC_DS03721,BMG_DS005282,Allergic asthma
+BMGC_DS03722,BMG_DS005284,Intrinsic asthma
+BMGC_DS03723,BMG_DS005286,Malt-workers' lung
+BMGC_DS03724,BMG_DS005287,Mushroom Worker's Lung
+BMGC_DS03725,BMG_DS005288,Maple-bark strippers' lung
+BMGC_DS03726,BMG_DS005289,Humidifier lung
+BMGC_DS03727,BMG_DS005296,Spontaneous tension pneumothorax
+BMGC_DS03728,BMG_DS005297,Abscess of lung and mediastinum
+BMGC_DS03729,BMG_DS005300,Pulmonary Alveolar Microlithiasis
+BMGC_DS03730,BMG_DS005301,Compensatory emphysema
+BMGC_DS03731,BMG_DS005302,Acute pulmonary edema
+BMGC_DS03732,BMG_DS005305,Tooth Ankylosis
+BMGC_DS03733,BMG_DS005307,Acute apical periodontitis of pulpal origin
+BMGC_DS03734,BMG_DS005309,Acute gingivitis
+BMGC_DS03735,BMG_DS005320,median rhomboid glossitis
+BMGC_DS03736,BMG_DS005321,Atrophy of tongue papillae
+BMGC_DS03737,BMG_DS005322,Acute gastric ulcer with hemorrhage
+BMGC_DS03738,BMG_DS005324,Acute gastric ulcer with perforation
+BMGC_DS03739,BMG_DS005334,Acute gastrojejunal ulcer with hemorrhage
+BMGC_DS03740,BMG_DS005340,Alcoholic gastritis
+BMGC_DS03741,BMG_DS005343,Chronic duodenal ileus
+BMGC_DS03742,BMG_DS005356,Crohn's disease of small intestine
+BMGC_DS03743,BMG_DS005357,Crohn's disease of large bowel
+BMGC_DS03744,BMG_DS005362,Functional diarrhea
+BMGC_DS03745,BMG_DS005365,anorectal stricture
+BMGC_DS03746,BMG_DS005366,Abscess of intestine
+BMGC_DS03747,BMG_DS005370,Chronic passive congestion of liver
+BMGC_DS03748,BMG_DS005377,Obstruction of gallbladder
+BMGC_DS03749,BMG_DS005378,Other diseases of biliary tract
+BMGC_DS03750,BMG_DS005379,perforation of bile duct
+BMGC_DS03751,BMG_DS005383,Pyeloureteritis cystica
+BMGC_DS03752,BMG_DS005384,Calculus of kidney and ureter
+BMGC_DS03753,BMG_DS005386,Hypertrophy of kidney
+BMGC_DS03754,BMG_DS005387,stricture or kinking of ureter
+BMGC_DS03755,BMG_DS005388,Calculus of lower urinary tract
+BMGC_DS03756,BMG_DS005389,Calculus in diverticulum of urinary bladder
+BMGC_DS03757,BMG_DS005391,Other chronic cystitis
+BMGC_DS03758,BMG_DS005392,Radiation cystitis
+BMGC_DS03759,BMG_DS005393,Other disorders of bladder
+BMGC_DS03760,BMG_DS005394,bladder diverticulum
+BMGC_DS03761,BMG_DS005395,Urethral abscess
+BMGC_DS03762,BMG_DS005396,Urethral syndrome
+BMGC_DS03763,BMG_DS005397,infective urethral stricture
+BMGC_DS03764,BMG_DS005398,urethral false passage
+BMGC_DS03765,BMG_DS005401,Prostatocystitis
+BMGC_DS03766,BMG_DS005404,Atrophy of prostate
+BMGC_DS03767,BMG_DS005409,Atrophy of testis
+BMGC_DS03768,BMG_DS005411,Chylocele of tunica vaginalis
+BMGC_DS03769,BMG_DS005412,male genital organ stricture
+BMGC_DS03770,BMG_DS005413,Fibrosclerosis of breast
+BMGC_DS03771,BMG_DS005416,Fat necrosis of breast
+BMGC_DS03772,BMG_DS005418,Acute salpingo-oophoritis
+BMGC_DS03773,BMG_DS005419,Chronic salpingo-oophoritis
+BMGC_DS03774,BMG_DS005424,Ulceration of vulva associated with another disorder
+BMGC_DS03775,BMG_DS005425,Endometriosis of ovary
+BMGC_DS03776,BMG_DS005426,Endometriosis of pelvic peritoneum
+BMGC_DS03777,BMG_DS005427,Endometriosis of rectovaginal septum and vagina
+BMGC_DS03778,BMG_DS005428,Endometriosis of intestine
+BMGC_DS03779,BMG_DS005429,Endometriosis in scar of skin
+BMGC_DS03780,BMG_DS005431,corpus luteum cyst
+BMGC_DS03781,BMG_DS005434,uterine polyp
+BMGC_DS03782,BMG_DS005435,Chronic subinvolution of uterus
+BMGC_DS03783,BMG_DS005440,leukoplakia of vagina
+BMGC_DS03784,BMG_DS005442,Atrophy of vulva
+BMGC_DS03785,BMG_DS005447,Postmenopausal atrophic vaginitis
+BMGC_DS03786,BMG_DS005450,female infertility of uterine origin
+BMGC_DS03787,BMG_DS005457,pregnancy disorder with abortive outcome
+BMGC_DS03788,BMG_DS005460,low implantation of placenta
+BMGC_DS03789,BMG_DS005461,mild pre-eclampsia
+BMGC_DS03790,BMG_DS005462,severe pre-eclampsia
+BMGC_DS03791,BMG_DS005469,supine hypotensive syndrome
+BMGC_DS03792,BMG_DS005471,puerperal pulmonary embolism
+BMGC_DS03793,BMG_DS005487,Acute lymphadenitis
+BMGC_DS03794,BMG_DS005491,Benign mucous membrane pemphigoid with ocular involvement
+BMGC_DS03795,BMG_DS005494,Chronic skin ulcer
+BMGC_DS03796,BMG_DS005496,Vibratory Urticaria
+BMGC_DS03797,BMG_DS005497,Arthropathy associated with infection
+BMGC_DS03798,BMG_DS005498,Arthropathy in Behcet's syndrome
+BMGC_DS03799,BMG_DS005500,Infective arthritis of shoulder region
+BMGC_DS03800,BMG_DS005501,septic arthritis
+BMGC_DS03801,BMG_DS005502,septic arthritis
+BMGC_DS03802,BMG_DS005503,septic arthritis
+BMGC_DS03803,BMG_DS005504,septic arthritis
+BMGC_DS03804,BMG_DS005505,septic arthritis
+BMGC_DS03805,BMG_DS005506,septic arthritis
+BMGC_DS03806,BMG_DS005507,Chondrocalcinosis due to dicalcium phosphate crystals
+BMGC_DS03807,BMG_DS005510,Acute polyarticular juvenile rheumatoid arthritis
+BMGC_DS03808,BMG_DS005511,Pauciarticular juvenile rheumatoid arthritis
+BMGC_DS03809,BMG_DS005512,Monoarticular juvenile rheumatoid arthritis
+BMGC_DS03810,BMG_DS005515,osteoarthritis
+BMGC_DS03811,BMG_DS005521,Transient arthropathy of the shoulder region
+BMGC_DS03812,BMG_DS005524,Articular cartilage disorder
+BMGC_DS03813,BMG_DS005529,hydrarthrosis
+BMGC_DS03814,BMG_DS005532,Villonodular synovitis
+BMGC_DS03815,BMG_DS005533,palindromic rheumatism
+BMGC_DS03816,BMG_DS005546,Kissing spine
+BMGC_DS03817,BMG_DS005547,Intervertebral disc disorder
+BMGC_DS03818,BMG_DS005554,Intervertebral Disc Degeneration
+BMGC_DS03819,BMG_DS005568,Hypermobility of the coccyx
+BMGC_DS03820,BMG_DS005571,Adhesive Capsulitis
+BMGC_DS03821,BMG_DS005572,Calcific tendinitis of shoulder
+BMGC_DS03822,BMG_DS005573,Bicipital tenosynovitis
+BMGC_DS03823,BMG_DS005577,pes anserinus tendinitis or bursitis
+BMGC_DS03824,BMG_DS005578,Tibial collateral ligament bursitis
+BMGC_DS03825,BMG_DS005579,Inflammation of subtendinous bursa of biceps femoris inferior muscle
+BMGC_DS03826,BMG_DS005580,Patellar tendonitis
+BMGC_DS03827,BMG_DS005582,Tibialis tendinitis
+BMGC_DS03828,BMG_DS005583,Heel Spur
+BMGC_DS03829,BMG_DS005588,tenosynovitis of foot and ankle
+BMGC_DS03830,BMG_DS005589,Specific bursitis often of occupational origin
+BMGC_DS03831,BMG_DS005591,ganglion or cyst of synovium/tendon/bursa
+BMGC_DS03832,BMG_DS005595,Infectious Myositis
+BMGC_DS03833,BMG_DS005596,plantar fibromatosis
+BMGC_DS03834,BMG_DS005597,Interstitial myositis
+BMGC_DS03835,BMG_DS005599,Acute osteomyelitis
+BMGC_DS03836,BMG_DS005605,Juvenile osteochondrosis of upper extremity
+BMGC_DS03837,BMG_DS005607,"Juvenile osteochondrosis of foot, NOS"
+BMGC_DS03838,BMG_DS005608,Other juvenile osteochondrosis
+BMGC_DS03839,BMG_DS005609,Idiopathic osteoporosis
+BMGC_DS03840,BMG_DS005610,osteonecrosis
+BMGC_DS03841,BMG_DS005611,Osteonecrosis of medial femoral condyle
+BMGC_DS03842,BMG_DS005612,osteonecrosis
+BMGC_DS03843,BMG_DS005622,congenital nervous system abnormality
+BMGC_DS03844,BMG_DS005623,congenital cystic eye
+BMGC_DS03845,BMG_DS005626,vascular malformation
+BMGC_DS03846,BMG_DS005631,Congenital insufficiency of mitral valve
+BMGC_DS03847,BMG_DS005632,congenital coronary artery anomaly
+BMGC_DS03848,BMG_DS005634,cleft lip/palate
+BMGC_DS03849,BMG_DS005635,cleft lip
+BMGC_DS03850,BMG_DS005636,aplasia of lacrimal and salivary glands
+BMGC_DS03851,BMG_DS005637,displacement of cardia through esophageal hiatus
+BMGC_DS03852,BMG_DS005638,Polycystic liver disease
+BMGC_DS03853,BMG_DS005639,congenital radioulnar synostosis
+BMGC_DS03854,BMG_DS005641,cervical rib disease
+BMGC_DS03855,BMG_DS005643,Fetal Malnutrition
+BMGC_DS03856,BMG_DS005652,Congenital Cytomegalovirus Infection
+BMGC_DS03857,BMG_DS005653,Omphalitis of the newborn
+BMGC_DS03858,BMG_DS005654,Neonatal infective mastitis
+BMGC_DS03859,BMG_DS005655,Hemolytic disease of fetus OR newborn due to RhD isoimmunization
+BMGC_DS03860,BMG_DS005657,Perinatal jaundice due to hepatocellular damage
+BMGC_DS03861,BMG_DS005658,Neonatal diabetes mellitus
+BMGC_DS03862,BMG_DS005659,Neonatal Myasthenia Gravis
+BMGC_DS03863,BMG_DS005660,Neonatal thyrotoxicosis
+BMGC_DS03864,BMG_DS005662,Neonatal hypoglycemia
+BMGC_DS03865,BMG_DS005664,transient neonatal thrombocytopenia
+BMGC_DS03866,BMG_DS005665,Disseminated intravascular coagulation in newborn
+BMGC_DS03867,BMG_DS005668,Anemia of prematurity
+BMGC_DS03868,BMG_DS005669,Transient neonatal neutropenia (disorder)
+BMGC_DS03869,BMG_DS005671,Perinatal intestinal perforation
+BMGC_DS03870,BMG_DS005675,Convulsions in the newborn
+BMGC_DS03871,BMG_DS005688,Conjunctival deposit
+BMGC_DS03872,BMG_DS005689,Corneal deposit
+BMGC_DS03873,BMG_DS005690,Nephrogenic Diabetes Insipidus
+BMGC_DS03874,BMG_DS005691,retinal ischemia
+BMGC_DS03875,BMG_DS005692,External Ophthalmoplegia
+BMGC_DS03876,BMG_DS005693,Polyarthralgia
+BMGC_DS03877,BMG_DS005694,Calculus in urethra
+BMGC_DS03878,BMG_DS005695,Adrenoleukodystrophy
+BMGC_DS03879,BMG_DS005696,Androgenetic Alopecia
+BMGC_DS03880,BMG_DS005697,Iron deficiency anemia
+BMGC_DS03881,BMG_DS005698,Polyarthritis
+BMGC_DS03882,BMG_DS005699,Christ-Siemens-Touraine syndrome
+BMGC_DS03883,BMG_DS005700,Hidrotic Ectodermal Dysplasia
+BMGC_DS03884,BMG_DS005701,"Granuloma, Giant Cell Reparative"
+BMGC_DS03885,BMG_DS005702,Miliaria Rubra
+BMGC_DS03886,BMG_DS005703,Malnutrition
+BMGC_DS03887,BMG_DS005704,Parapsoriasis en Plaques
+BMGC_DS03888,BMG_DS005707,uterine inversion
+BMGC_DS03889,BMG_DS005712,Caroli Disease
+BMGC_DS03890,BMG_DS005713,AIDS-Related Opportunistic Infections
+BMGC_DS03891,BMG_DS005714,"Colitis, Ischemic"
+BMGC_DS03892,BMG_DS005715,cutaneous porphyria
+BMGC_DS03893,BMG_DS005716,Hereditary Coproporphyria
+BMGC_DS03894,BMG_DS005717,Variegate Porphyria
+BMGC_DS03895,BMG_DS005718,"Porphyrias, Hepatic"
+BMGC_DS03896,BMG_DS005719,Prion Diseases
+BMGC_DS03897,BMG_DS005720,Immunoglobulin A deficiency (disorder)
+BMGC_DS03898,BMG_DS005721,Immunoglobulin G deficiency (disorder)
+BMGC_DS03899,BMG_DS005722,"Akathisia, Tardive"
+BMGC_DS03900,BMG_DS005723,"Akathisia, Drug-Induced"
+BMGC_DS03901,BMG_DS005724,"Liver Failure, Acute"
+BMGC_DS03902,BMG_DS005725,Acute intermittent porphyria
+BMGC_DS03903,BMG_DS005726,Porphyria Cutanea Tarda
+BMGC_DS03904,BMG_DS005727,Erythropoietic Protoporphyria
+BMGC_DS03905,BMG_DS005728,Hepatoerythropoietic Porphyria
+BMGC_DS03906,BMG_DS005729,Anisakiasis
+BMGC_DS03907,BMG_DS005734,"Skin Diseases, Bacterial"
+BMGC_DS03908,BMG_DS005735,"Skin Diseases, Viral"
+BMGC_DS03909,BMG_DS005736,Oxyurida Infections
+BMGC_DS03910,BMG_DS005738,Angelman Syndrome
+BMGC_DS03911,BMG_DS005741,Root Caries
+BMGC_DS03912,BMG_DS005742,Gastric outlet obstruction
+BMGC_DS03913,BMG_DS005743,Mitochondrial Encephalomyopathies
+BMGC_DS03914,BMG_DS005744,Megaconial Myopathies
+BMGC_DS03915,BMG_DS005745,Pleoconial Myopathies
+BMGC_DS03916,BMG_DS005746,Mitochondrial Myopathies
+BMGC_DS03917,BMG_DS005747,MELAS Syndrome
+BMGC_DS03918,BMG_DS005748,MERRF Syndrome
+BMGC_DS03919,BMG_DS005749,Chronic progressive external ophthalmoplegia
+BMGC_DS03920,BMG_DS005750,Caliciviridae Infections
+BMGC_DS03921,BMG_DS005751,neurofibromatosis
+BMGC_DS03922,BMG_DS005752,Tick-Borne Infections
+BMGC_DS03923,BMG_DS005753,Tick-Borne Diseases
+BMGC_DS03924,BMG_DS005754,HELLP Syndrome
+BMGC_DS03925,BMG_DS005755,Right Ventricular Hypertrophy
+BMGC_DS03926,BMG_DS005756,Kallmann Syndrome
+BMGC_DS03927,BMG_DS005759,"Skin Diseases, Vascular"
+BMGC_DS03928,BMG_DS005760,"Dermatitis, Allergic Contact"
+BMGC_DS03929,BMG_DS005761,"Dermatitis, Irritant"
+BMGC_DS03930,BMG_DS005762,"Dermatitis, Photoallergic"
+BMGC_DS03931,BMG_DS005763,"Dermatitis, Phototoxic"
+BMGC_DS03932,BMG_DS005764,hyperpigmentation of the skin
+BMGC_DS03933,BMG_DS005765,Hypopigmentation disorder
+BMGC_DS03934,BMG_DS005766,Hidradenitis Suppurativa
+BMGC_DS03935,BMG_DS005767,"Porokeratosis, Palmoplantar"
+BMGC_DS03936,BMG_DS005768,porokeratosis
+BMGC_DS03937,BMG_DS005769,Lichenoid Eruptions
+BMGC_DS03938,BMG_DS005770,Lichen Nitidus
+BMGC_DS03939,BMG_DS005775,Mucinoses
+BMGC_DS03940,BMG_DS005776,"Aneurysm, Ruptured"
+BMGC_DS03941,BMG_DS005777,abdominal aortic aneurysm
+BMGC_DS03942,BMG_DS005778,thoracic aortic aneurysm
+BMGC_DS03943,BMG_DS005780,Citrullinemia
+BMGC_DS03944,BMG_DS005781,Dubowitz syndrome
+BMGC_DS03945,BMG_DS005782,Johanson-Blizzard syndrome
+BMGC_DS03946,BMG_DS005783,Russell-Silver syndrome
+BMGC_DS03947,BMG_DS005784,Smith-Lemli-Opitz Syndrome
+BMGC_DS03948,BMG_DS005785,Sotos' syndrome
+BMGC_DS03949,BMG_DS005787,Van der Woude syndrome
+BMGC_DS03950,BMG_DS005788,Saethre-Chotzen Syndrome
+BMGC_DS03951,BMG_DS005789,Multiple synostosis syndrome
+BMGC_DS03952,BMG_DS005790,Aarskog syndrome
+BMGC_DS03953,BMG_DS005791,Williams Syndrome
+BMGC_DS03954,BMG_DS005792,Thrombocytopenia-Absent Radius Syndrome
+BMGC_DS03955,BMG_DS005793,LEOPARD Syndrome
+BMGC_DS03956,BMG_DS005794,Asplenia Syndrome
+BMGC_DS03957,BMG_DS005796,Centronuclear myopathy
+BMGC_DS03958,BMG_DS005797,Aicardi's syndrome
+BMGC_DS03959,BMG_DS005798,"corpus callosum, agenesis of"
+BMGC_DS03960,BMG_DS005800,Larsen syndrome
+BMGC_DS03961,BMG_DS005801,"autoimmune hemolytic anemia, cold type"
+BMGC_DS03962,BMG_DS005803,Post-inflammatory pulmonary fibrosis
+BMGC_DS03963,BMG_DS005804,Intestinal infectious disease (disorder)
+BMGC_DS03964,BMG_DS005809,Other disorders of central nervous system
+BMGC_DS03965,BMG_DS005819,Hypoplastic anemia
+BMGC_DS03966,BMG_DS005820,breast fibroadenoma
+BMGC_DS03967,BMG_DS005821,Oligohydramnios sequence
+BMGC_DS03968,BMG_DS005823,Cerebral Hypoxia-Ischemia
+BMGC_DS03969,BMG_DS005825,Glomerulosclerosis (disorder)
+BMGC_DS03970,BMG_DS005829,reproductive system neoplasm
+BMGC_DS03971,BMG_DS005830,Urinary tract obstruction
+BMGC_DS03972,BMG_DS005832,cribriform carcinoma
+BMGC_DS03973,BMG_DS005833,granular cell carcinoma
+BMGC_DS03974,BMG_DS005834,tubular adenocarcinoma
+BMGC_DS03975,BMG_DS005835,follicular adenoma
+BMGC_DS03976,BMG_DS005836,microcystic adenoma
+BMGC_DS03977,BMG_DS005837,papillary adenoma
+BMGC_DS03978,BMG_DS005838,"Infections, Arenavirus"
+BMGC_DS03979,BMG_DS005840,sarcomatoid carcinoma
+BMGC_DS03980,BMG_DS005843,Alpers Syndrome
+BMGC_DS03981,BMG_DS005844,Pelizaeus-Merzbacher Disease
+BMGC_DS03982,BMG_DS005845,Roussy-Levy syndrome
+BMGC_DS03983,BMG_DS005847,"Diabetes, Autoimmune"
+BMGC_DS03984,BMG_DS005849,dysplastic nevus syndrome
+BMGC_DS03985,BMG_DS005850,Chronic Cystic Mastitis
+BMGC_DS03986,BMG_DS005851,fibromyxoid tumor
+BMGC_DS03987,BMG_DS005852,subependymal giant cell astrocytoma
+BMGC_DS03988,BMG_DS005853,myxopapillary ependymoma
+BMGC_DS03989,BMG_DS005854,choroid plexus papilloma
+BMGC_DS03990,BMG_DS005855,epithelioid hemangioma
+BMGC_DS03991,BMG_DS005856,intramuscular hemangioma
+BMGC_DS03992,BMG_DS005857,enterocele
+BMGC_DS03993,BMG_DS005858,epithelioid leiomyosarcoma
+BMGC_DS03994,BMG_DS005859,myxoid leiomyosarcoma
+BMGC_DS03995,BMG_DS005861,pleomorphic lipoma
+BMGC_DS03996,BMG_DS005862,dedifferentiated liposarcoma
+BMGC_DS03997,BMG_DS005863,pleomorphic liposarcoma
+BMGC_DS03998,BMG_DS005865,medullomyoblastoma with myogenic differentiation
+BMGC_DS03999,BMG_DS005866,germ cell tumor
+BMGC_DS04000,BMG_DS005869,squamous papilloma
+BMGC_DS04001,BMG_DS005870,papillomatosis
+BMGC_DS04002,BMG_DS005872,pineoblastoma
+BMGC_DS04003,BMG_DS005874,Algoneurodystrophy
+BMGC_DS04004,BMG_DS005875,epithelioid sarcoma
+BMGC_DS04005,BMG_DS005876,spindle cell sarcoma
+BMGC_DS04006,BMG_DS005877,thymic carcinoma
+BMGC_DS04007,BMG_DS005878,HIV Encephalopathy
+BMGC_DS04008,BMG_DS005879,Fatal Familial Insomnia
+BMGC_DS04009,BMG_DS005880,"Infections, Calicivirus"
+BMGC_DS04010,BMG_DS005881,Photoallergy
+BMGC_DS04011,BMG_DS005882,"Pneumonia, Interstitial"
+BMGC_DS04012,BMG_DS005883,"Lung Diseases, Interstitial"
+BMGC_DS04013,BMG_DS005884,Microvascular Angina
+BMGC_DS04014,BMG_DS005885,Focal Epithelial Hyperplasia
+BMGC_DS04015,BMG_DS005886,Hyperandrogenism
+BMGC_DS04016,BMG_DS005887,"Myelinolysis, Central Pontine"
+BMGC_DS04017,BMG_DS005888,Kleine-Levin Syndrome
+BMGC_DS04018,BMG_DS005889,neuroectodermal tumor
+BMGC_DS04019,BMG_DS005892,WAGR Syndrome
+BMGC_DS04020,BMG_DS005893,CREST Syndrome
+BMGC_DS04021,BMG_DS005894,"Lichen Planus, Oral"
+BMGC_DS04022,BMG_DS005895,Idiopathic Hypereosinophilic Syndrome
+BMGC_DS04023,BMG_DS005896,Loeffler's Endocarditis
+BMGC_DS04024,BMG_DS005897,Stunned Myocardium
+BMGC_DS04025,BMG_DS005898,Myocardial Stunning
+BMGC_DS04026,BMG_DS005900,"Myopathies, Nemaline"
+BMGC_DS04027,BMG_DS005901,Community-Acquired Infections
+BMGC_DS04028,BMG_DS005903,Cytomegalovirus Retinitis
+BMGC_DS04029,BMG_DS005904,anaplastic large cell lymphoma
+BMGC_DS04030,BMG_DS005905,lymphomatoid papulosis
+BMGC_DS04031,BMG_DS005906,oral hairy leukoplakia
+BMGC_DS04032,BMG_DS005909,"Amyloid Neuropathies, Familial"
+BMGC_DS04033,BMG_DS005910,Amyloid Neuropathies
+BMGC_DS04034,BMG_DS005912,Canavan Disease
+BMGC_DS04035,BMG_DS005913,Exfoliation Syndrome
+BMGC_DS04036,BMG_DS005915,"Tuberculosis, Drug-Resistant"
+BMGC_DS04037,BMG_DS005916,"Tuberculosis, Multidrug-Resistant"
+BMGC_DS04038,BMG_DS005918,Endolymphatic Hydrops
+BMGC_DS04039,BMG_DS005924,Flavivirus Infections
+BMGC_DS04040,BMG_DS005930,Cardiovirus Infections
+BMGC_DS04041,BMG_DS005932,cystic hygroma
+BMGC_DS04042,BMG_DS005933,adenomyoma
+BMGC_DS04043,BMG_DS005934,adenosquamous carcinoma
+BMGC_DS04044,BMG_DS005935,hepatoblastoma
+BMGC_DS04045,BMG_DS005936,malignant mixed neoplasm
+BMGC_DS04046,BMG_DS005937,carcinosarcoma
+BMGC_DS04047,BMG_DS005939,pulmonary blastoma
+BMGC_DS04048,BMG_DS005940,endometrioid stromal sarcoma
+BMGC_DS04049,BMG_DS005941,tumor of adipose tissue
+BMGC_DS04050,BMG_DS005942,angiolipoma
+BMGC_DS04051,BMG_DS005943,angiomyolipoma
+BMGC_DS04052,BMG_DS005944,myxoid liposarcoma
+BMGC_DS04053,BMG_DS005946,mesenchymal chondrosarcoma
+BMGC_DS04054,BMG_DS005947,bone giant cell tumor
+BMGC_DS04055,BMG_DS005948,osteosarcoma
+BMGC_DS04056,BMG_DS005950,juxtacortical osteosarcoma
+BMGC_DS04057,BMG_DS005951,fibroblastic neoplasm
+BMGC_DS04058,BMG_DS005952,benign fibrous histiocytoma
+BMGC_DS04059,BMG_DS005953,dermatofibrosarcoma protuberans
+BMGC_DS04060,BMG_DS005955,breast fibroadenoma
+BMGC_DS04061,BMG_DS005956,clear cell sarcoma
+BMGC_DS04062,BMG_DS005957,small cell sarcoma
+BMGC_DS04063,BMG_DS005958,angioleiomyoma
+BMGC_DS04064,BMG_DS005959,leiomyomatosis
+BMGC_DS04065,BMG_DS005960,alveolar rhabdomyosarcoma
+BMGC_DS04066,BMG_DS005961,embryonal rhabdomyosarcoma
+BMGC_DS04067,BMG_DS005962,alveolar soft part sarcoma
+BMGC_DS04068,BMG_DS005963,smooth muscle tumor
+BMGC_DS04069,BMG_DS005964,embryonal carcinoma
+BMGC_DS04070,BMG_DS005965,germinoma
+BMGC_DS04071,BMG_DS005967,primitive neuroectodermal tumor
+BMGC_DS04072,BMG_DS005968,teratocarcinoma
+BMGC_DS04073,BMG_DS005969,placental site trophoblastic tumor
+BMGC_DS04074,BMG_DS005970,adrenal cortex adenoma
+BMGC_DS04075,BMG_DS005971,hepatocellular adenoma
+BMGC_DS04076,BMG_DS005972,eccrine acrospiroma
+BMGC_DS04077,BMG_DS005973,hidrocystoma
+BMGC_DS04078,BMG_DS005974,syringoma
+BMGC_DS04079,BMG_DS005975,villous adenoma
+BMGC_DS04080,BMG_DS005976,adenomatoid tumor
+BMGC_DS04081,BMG_DS005977,clear cell adenocarcinoma
+BMGC_DS04082,BMG_DS005978,thyroid gland follicular carcinoma
+BMGC_DS04083,BMG_DS005980,sebaceous adenocarcinoma
+BMGC_DS04084,BMG_DS005981,acinar cell carcinoma
+BMGC_DS04085,BMG_DS005982,adrenal cortex carcinoma
+BMGC_DS04086,BMG_DS005983,endometrial carcinoma
+BMGC_DS04087,BMG_DS005984,breast lobular carcinoma
+BMGC_DS04088,BMG_DS005985,mucoepidermoid carcinoma
+BMGC_DS04089,BMG_DS005986,neuroendocrine carcinoma
+BMGC_DS04090,BMG_DS005987,signet ring cell carcinoma
+BMGC_DS04091,BMG_DS005989,cholangiocarcinoma
+BMGC_DS04092,BMG_DS005990,mucinous cystadenocarcinoma
+BMGC_DS04093,BMG_DS005991,papillary cystadenocarcinoma
+BMGC_DS04094,BMG_DS005992,serous cystadenocarcinoma
+BMGC_DS04095,BMG_DS005993,hilar cholangiocarcinoma
+BMGC_DS04096,BMG_DS005994,lung giant cell carcinoma
+BMGC_DS04097,BMG_DS005995,large cell carcinoma
+BMGC_DS04098,BMG_DS005996,verrucous carcinoma
+BMGC_DS04099,BMG_DS005999,basal cell neoplasm
+BMGC_DS04100,BMG_DS006000,pilomatrixoma
+BMGC_DS04101,BMG_DS006001,intraductal papilloma
+BMGC_DS04102,BMG_DS006003,ganglioglioma
+BMGC_DS04103,BMG_DS006004,esthesioneuroblastoma
+BMGC_DS04104,BMG_DS006005,ganglioneuroblastoma
+BMGC_DS04105,BMG_DS006006,central neurocytoma
+BMGC_DS04106,BMG_DS006007,squamous cell neoplasm
+BMGC_DS04107,BMG_DS006008,inverted papilloma
+BMGC_DS04108,BMG_DS006010,Sertoli-Leydig cell tumor
+BMGC_DS04109,BMG_DS006011,sex cord-stromal tumor
+BMGC_DS04110,BMG_DS006012,subependymoma
+BMGC_DS04111,BMG_DS006013,gliosarcoma
+BMGC_DS04112,BMG_DS006014,nerve sheath neoplasm
+BMGC_DS04113,BMG_DS006015,plexiform neurofibroma
+BMGC_DS04114,BMG_DS006016,neurofibrosarcoma
+BMGC_DS04115,BMG_DS006018,capillary hemangioma
+BMGC_DS04116,BMG_DS006019,hemangioblastoma
+BMGC_DS04117,BMG_DS006020,amelanotic melanoma
+BMGC_DS04118,BMG_DS006021,blue nevus
+BMGC_DS04119,BMG_DS006024,spitz nevus
+BMGC_DS04120,BMG_DS006025,rhabdoid tumor
+BMGC_DS04121,BMG_DS006026,"T-Lymphocytopenia, Idiopathic CD4-Positive"
+BMGC_DS04122,BMG_DS006028,Coronavirus Infections
+BMGC_DS04123,BMG_DS006032,neuroendocrine neoplasm
+BMGC_DS04124,BMG_DS006033,congenital deformities of limbs
+BMGC_DS04125,BMG_DS006036,Bartholin gland neoplasm
+BMGC_DS04126,BMG_DS006038,brain cancer
+BMGC_DS04127,BMG_DS006039,uveal melanoma
+BMGC_DS04128,BMG_DS006040,salivary gland cancer
+BMGC_DS04129,BMG_DS006041,lip and oral cavity carcinoma
+BMGC_DS04130,BMG_DS006045,Pfeiffer Syndrome
+BMGC_DS04131,BMG_DS006046,Acrodysostosis
+BMGC_DS04132,BMG_DS006047,"adactylia, unilateral"
+BMGC_DS04133,BMG_DS006048,"ARTHROGRYPOSIS, DISTAL, TYPE 1"
+BMGC_DS04134,BMG_DS006049,"Blepharophimosis, Ptosis, and Epicanthus Inversus"
+BMGC_DS04135,BMG_DS006050,brachydactyly type D
+BMGC_DS04136,BMG_DS006051,"ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA"
+BMGC_DS04137,BMG_DS006052,congenital contractural arachnodactyly
+BMGC_DS04138,BMG_DS006053,benign neonatal seizures
+BMGC_DS04139,BMG_DS006055,Goldenhar Syndrome with Ipsilateral Radial Defect
+BMGC_DS04140,BMG_DS006056,achondrogenesis type II
+BMGC_DS04141,BMG_DS006057,Aase Smith syndrome
+BMGC_DS04142,BMG_DS006058,KBG syndrome
+BMGC_DS04143,BMG_DS006059,"macrocephaly, benign familial"
+BMGC_DS04144,BMG_DS006060,"Maxillonasal dysplasia, Binder type"
+BMGC_DS04145,BMG_DS006061,Microcephaly autosomal dominant
+BMGC_DS04146,BMG_DS006063,postaxial polydactyly
+BMGC_DS04147,BMG_DS006064,RETINITIS PIGMENTOSA 1
+BMGC_DS04148,BMG_DS006065,schizophrenia 1
+BMGC_DS04149,BMG_DS006066,Shprintzen syndrome
+BMGC_DS04150,BMG_DS006067,VACTERL association
+BMGC_DS04151,BMG_DS006068,Medium-chain acyl-coenzyme A dehydrogenase deficiency
+BMGC_DS04152,BMG_DS006069,Long chain acyl-CoA dehydrogenase deficiency
+BMGC_DS04153,BMG_DS006070,"CATARACT 46, JUVENILE-ONSET, WITH OR WITHOUT ARRHYTHMIC CARDIOMYOPATHY"
+BMGC_DS04154,BMG_DS006071,Cerebrooculofacioskeletal Syndrome 1
+BMGC_DS04155,BMG_DS006072,choanal atresia
+BMGC_DS04156,BMG_DS006073,amniotic band syndrome
+BMGC_DS04157,BMG_DS006074,Diastrophic dysplasia
+BMGC_DS04158,BMG_DS006075,Fryns syndrome
+BMGC_DS04159,BMG_DS006077,Bixler Christian Gorlin syndrome
+BMGC_DS04160,BMG_DS006078,Childhood hypophosphatasia (disorder)
+BMGC_DS04161,BMG_DS006079,multiple intestinal atresia
+BMGC_DS04162,BMG_DS006080,Cartilage-hair hypoplasia
+BMGC_DS04163,BMG_DS006082,Biotinidase Deficiency
+BMGC_DS04164,BMG_DS006083,"Niemann-Pick Disease, Type C"
+BMGC_DS04165,BMG_DS006084,"Blount disease, infantile"
+BMGC_DS04166,BMG_DS006085,Weaver-Like Syndrome
+BMGC_DS04167,BMG_DS006086,Craniofrontonasal dysplasia
+BMGC_DS04168,BMG_DS006087,FG syndrome
+BMGC_DS04169,BMG_DS006088,"RUSSELL-SILVER SYNDROME, X-LINKED"
+BMGC_DS04170,BMG_DS006091,metabolic acidosis
+BMGC_DS04171,BMG_DS006092,Ketoacidosis
+BMGC_DS04172,BMG_DS006093,Hereditary orotic aciduria
+BMGC_DS04173,BMG_DS006094,Xanthinuria (disorder)
+BMGC_DS04174,BMG_DS006095,Acquired partial lipodystrophy
+BMGC_DS04175,BMG_DS006096,Rotor Syndrome
+BMGC_DS04176,BMG_DS006097,Histidinemia
+BMGC_DS04177,BMG_DS006098,Cystathioninuria
+BMGC_DS04178,BMG_DS006099,Hyperammonemia (disorder)
+BMGC_DS04179,BMG_DS006101,Hypothalamic hypothyroidism
+BMGC_DS04180,BMG_DS006102,"Hyperparathyroidism, Primary"
+BMGC_DS04181,BMG_DS006103,Mauriac's syndrome
+BMGC_DS04182,BMG_DS006106,Malignant Atrophic Papulosis
+BMGC_DS04183,BMG_DS006108,systemic mastocytosis
+BMGC_DS04184,BMG_DS006112,Sickle cell-beta-thalassemia
+BMGC_DS04185,BMG_DS006113,Thalassemia-hemoglobin C disease
+BMGC_DS04186,BMG_DS006116,Cyclic neutropenia
+BMGC_DS04187,BMG_DS006117,Kasabach-Merritt syndrome
+BMGC_DS04188,BMG_DS006118,X-linked agammaglobulinemia
+BMGC_DS04189,BMG_DS006122,Familial generalized lipodystrophy
+BMGC_DS04190,BMG_DS006125,Acrodermatitis enteropathica
+BMGC_DS04191,BMG_DS006130,Liddle Syndrome
+BMGC_DS04192,BMG_DS006131,High output heart failure
+BMGC_DS04193,BMG_DS006132,"Syncope, Carotid Sinus"
+BMGC_DS04194,BMG_DS006135,Chronic berylliosis
+BMGC_DS04195,BMG_DS006137,Welander Distal Myopathy
+BMGC_DS04196,BMG_DS006138,paramyotonia congenita of Von Eulenburg
+BMGC_DS04197,BMG_DS006142,Subacute myelo-optic neuropathy
+BMGC_DS04198,BMG_DS006143,Mobius Syndrome
+BMGC_DS04199,BMG_DS006144,Behr syndrome
+BMGC_DS04200,BMG_DS006145,Subacute Combined Degeneration
+BMGC_DS04201,BMG_DS006146,Anterior Spinal Artery Syndrome
+BMGC_DS04202,BMG_DS006147,postpartum depression
+BMGC_DS04203,BMG_DS006151,Paroxysmal hypertension
+BMGC_DS04204,BMG_DS006153,multifocal atrial tachycardia
+BMGC_DS04205,BMG_DS006154,Motor Disorders
+BMGC_DS04206,BMG_DS006157,Hemiballismus
+BMGC_DS04207,BMG_DS006159,volvulus of midgut
+BMGC_DS04208,BMG_DS006163,Centriacinar Emphysema
+BMGC_DS04209,BMG_DS006168,Angular cheilitis
+BMGC_DS04210,BMG_DS006169,Mesangial proliferative glomerulonephritis
+BMGC_DS04211,BMG_DS006170,Rapidly progressive glomerulonephritis
+BMGC_DS04212,BMG_DS006173,Seborrheic dermatitis of scalp
+BMGC_DS04213,BMG_DS006176,Trichiasis
+BMGC_DS04214,BMG_DS006177,Dystrophia unguium
+BMGC_DS04215,BMG_DS006178,Poliosis
+BMGC_DS04216,BMG_DS006182,Elastosis perforans serpiginosa
+BMGC_DS04217,BMG_DS006184,Relative erythrocytosis
+BMGC_DS04218,BMG_DS006185,Paget disease of the penis
+BMGC_DS04219,BMG_DS006187,"Synovioma, benign"
+BMGC_DS04220,BMG_DS006188,chondromyxoid fibroma
+BMGC_DS04221,BMG_DS006190,Hereditary lymphedema and yellow nails
+BMGC_DS04222,BMG_DS006191,megalencephaly
+BMGC_DS04223,BMG_DS006192,brachydactyly
+BMGC_DS04224,BMG_DS006193,bifid nose
+BMGC_DS04225,BMG_DS006204,Non-Bacterial Thrombotic Endocarditis
+BMGC_DS04226,BMG_DS006206,Atrophic Vaginitis
+BMGC_DS04227,BMG_DS006209,Pituitary cachexia
+BMGC_DS04228,BMG_DS006210,Pituitary-dependent Cushing's disease
+BMGC_DS04229,BMG_DS006213,Vitamin D-dependent rickets
+BMGC_DS04230,BMG_DS006215,alpha 1-Antitrypsin Deficiency
+BMGC_DS04231,BMG_DS006216,Brachial Plexus Neuritis
+BMGC_DS04232,BMG_DS006221,nontoxic goiter
+BMGC_DS04233,BMG_DS006222,vaginal discharge
+BMGC_DS04234,BMG_DS006230,Premature aging syndrome
+BMGC_DS04235,BMG_DS006270,Orthostatic proteinuria
+BMGC_DS04236,BMG_DS006298,Primary physiologic amenorrhea
+BMGC_DS04237,BMG_DS006299,Secondary physiologic amenorrhea
+BMGC_DS04238,BMG_DS006304,spermatogenic failure 4
+BMGC_DS04239,BMG_DS006325,animal phobia
+BMGC_DS04240,BMG_DS006327,anterograde amnesia
+BMGC_DS04241,BMG_DS006342,hyperekplexia
+BMGC_DS04242,BMG_DS006346,"Neuralgia, Atypical"
+BMGC_DS04243,BMG_DS006347,"Neuralgia, Stump"
+BMGC_DS04244,BMG_DS006355,"Taste Disorder, Primary"
+BMGC_DS04245,BMG_DS006356,"Taste Disorder, Primary, Sweet"
+BMGC_DS04246,BMG_DS006357,"Taste Disorder, Primary, Salt"
+BMGC_DS04247,BMG_DS006358,"Taste Disorder, Primary, Bitter"
+BMGC_DS04248,BMG_DS006360,"Taste Disorder, Anterior Tongue"
+BMGC_DS04249,BMG_DS006361,"Taste Disorder, Secondary"
+BMGC_DS04250,BMG_DS006362,"Taste Disorder, Secondary, Sweet"
+BMGC_DS04251,BMG_DS006363,"Taste Disorder, Secondary, Salt"
+BMGC_DS04252,BMG_DS006364,"Taste Disorder, Secondary, Bitter"
+BMGC_DS04253,BMG_DS006367,"Taste Disorder, Posterior Tongue"
+BMGC_DS04254,BMG_DS006370,"Motor Disorder, Vagus Nerve"
+BMGC_DS04255,BMG_DS006371,"Sensory Disorder, Vagus Nerve"
+BMGC_DS04256,BMG_DS006381,visual cortex disorder
+BMGC_DS04257,BMG_DS006395,prosopagnosia
+BMGC_DS04258,BMG_DS006396,ideomotor apraxia
+BMGC_DS04259,BMG_DS006397,Generalized seizures
+BMGC_DS04260,BMG_DS006399,Clonic Seizures
+BMGC_DS04261,BMG_DS006419,"Vertigo, Brain Stem"
+BMGC_DS04262,BMG_DS006420,acneiform dermatitis
+BMGC_DS04263,BMG_DS006421,Annular Erythema
+BMGC_DS04264,BMG_DS006426,Simple Partial Seizures
+BMGC_DS04265,BMG_DS006427,Motor cortex epilepsy
+BMGC_DS04266,BMG_DS006429,Peripheral motor neuropathy
+BMGC_DS04267,BMG_DS006430,"Neuritis, Sensory"
+BMGC_DS04268,BMG_DS006431,toxic encephalopathy
+BMGC_DS04269,BMG_DS006435,Cycloplegia
+BMGC_DS04270,BMG_DS006436,Keratopathy
+BMGC_DS04271,BMG_DS006445,Granulomatous hepatitis
+BMGC_DS04272,BMG_DS006447,Ketonemia
+BMGC_DS04273,BMG_DS006451,Paroxysmal atrial fibrillation
+BMGC_DS04274,BMG_DS006453,peripheral ischemia
+BMGC_DS04275,BMG_DS006458,"Heart Failure, Right-Sided"
+BMGC_DS04276,BMG_DS006463,Submandibular lymphadenitis
+BMGC_DS04277,BMG_DS006464,Cervical lymphadenopathy
+BMGC_DS04278,BMG_DS006466,qualitative platelet defect
+BMGC_DS04279,BMG_DS006467,Proliferative glomerulonephritis
+BMGC_DS04280,BMG_DS006471,urothelial papilloma
+BMGC_DS04281,BMG_DS006473,malignant ovarian cyst
+BMGC_DS04282,BMG_DS006474,gallbladder carcinoma
+BMGC_DS04283,BMG_DS006476,neonatal leukemia
+BMGC_DS04284,BMG_DS006477,Neonatal urinary tract infection
+BMGC_DS04285,BMG_DS006478,Neonatal encephalopathy
+BMGC_DS04286,BMG_DS006479,congenital diaphragmatic hernia
+BMGC_DS04287,BMG_DS006481,Neonatal diarrhea
+BMGC_DS04288,BMG_DS006485,hypertrichosis lanuginosa congenita
+BMGC_DS04289,BMG_DS006486,Mononeuritis
+BMGC_DS04290,BMG_DS006493,Cerebral atrophy
+BMGC_DS04291,BMG_DS006494,Zinc deficiency
+BMGC_DS04292,BMG_DS006495,Clostridium difficile diarrhea
+BMGC_DS04293,BMG_DS006498,exocrine pancreatic carcinoma
+BMGC_DS04294,BMG_DS006503,Fetal valproate syndrome
+BMGC_DS04295,BMG_DS006505,Congenital hearing disorder
+BMGC_DS04296,BMG_DS006506,"Polyposis, Gastric"
+BMGC_DS04297,BMG_DS006512,Gastrointestinal obstruction
+BMGC_DS04298,BMG_DS006514,Pick Disease of the Brain
+BMGC_DS04299,BMG_DS006516,Alcohol withdrawal syndrome
+BMGC_DS04300,BMG_DS006517,Alcohol Related Disorders
+BMGC_DS04301,BMG_DS006519,Cannabis-Related Disorder
+BMGC_DS04302,BMG_DS006520,bipolar I disorder
+BMGC_DS04303,BMG_DS006521,bipolar disorder
+BMGC_DS04304,BMG_DS006522,bipolar II disorder
+BMGC_DS04305,BMG_DS006523,childhood disintegrative disorder
+BMGC_DS04306,BMG_DS006524,Asperger syndrome
+BMGC_DS04307,BMG_DS006526,dissociative amnesia
+BMGC_DS04308,BMG_DS006528,specific phobia
+BMGC_DS04309,BMG_DS006531,Chronobiology Disorders
+BMGC_DS04310,BMG_DS006533,expressive language disorder
+BMGC_DS04311,BMG_DS006534,mixed receptive-expressive language disorder
+BMGC_DS04312,BMG_DS006535,Neuroleptic-induced parkinsonism
+BMGC_DS04313,BMG_DS006542,substance-related disorder
+BMGC_DS04314,BMG_DS006543,Alcohol-Induced Disorders
+BMGC_DS04315,BMG_DS006545,dermoid cyst of ovary
+BMGC_DS04316,BMG_DS006547,Gastrointestinal ulcer
+BMGC_DS04317,BMG_DS006551,Toxic amblyopia
+BMGC_DS04318,BMG_DS006552,Glucose-6-phosphate dehydrogenase deficiency anemia
+BMGC_DS04319,BMG_DS006554,appendix adenocarcinoma
+BMGC_DS04320,BMG_DS006556,Invasive aspergillosis
+BMGC_DS04321,BMG_DS006558,Autonomic Dysreflexia
+BMGC_DS04322,BMG_DS006559,Bartholin gland adenocarcinoma
+BMGC_DS04323,BMG_DS006560,extrahepatic bile duct carcinoma
+BMGC_DS04324,BMG_DS006561,"Botulism, Infantile"
+BMGC_DS04325,BMG_DS006562,ependymal tumor of brain
+BMGC_DS04326,BMG_DS006563,breast phyllodes tumor
+BMGC_DS04327,BMG_DS006565,intraductal breast papilloma
+BMGC_DS04328,BMG_DS006567,Concentric hypertrophic cardiomyopathy
+BMGC_DS04329,BMG_DS006570,Cerebral Angiitis
+BMGC_DS04330,BMG_DS006571,"Xanthomatosis, Cerebrotendinous"
+BMGC_DS04331,BMG_DS006572,"Chorea, Senile"
+BMGC_DS04332,BMG_DS006574,Chronic intestinal pseudo-obstruction
+BMGC_DS04333,BMG_DS006575,Secondary Biliary Cholangitis
+BMGC_DS04334,BMG_DS006576,"Colitis, Collagenous"
+BMGC_DS04335,BMG_DS006578,Cranial Epidural Abscess
+BMGC_DS04336,BMG_DS006582,Acute endometritis
+BMGC_DS04337,BMG_DS006586,Lennox-Gastaut syndrome
+BMGC_DS04338,BMG_DS006590,Eunuchism
+BMGC_DS04339,BMG_DS006592,fallopian tube carcinoma
+BMGC_DS04340,BMG_DS006593,Necrotizing fasciitis
+BMGC_DS04341,BMG_DS006597,focal embolic glomerulonephritis
+BMGC_DS04342,BMG_DS006599,heart sarcoma
+BMGC_DS04343,BMG_DS006602,Hemoglobin E disease
+BMGC_DS04344,BMG_DS006608,"Myositis, Inclusion Body"
+BMGC_DS04345,BMG_DS006609,small intestine carcinoma
+BMGC_DS04346,BMG_DS006610,small intestine leiomyoma
+BMGC_DS04347,BMG_DS006611,gastrointestinal stromal tumor
+BMGC_DS04348,BMG_DS006612,kidney fibrosarcoma
+BMGC_DS04349,BMG_DS006616,liver hemangioma
+BMGC_DS04350,BMG_DS006618,Lymphedema praecox
+BMGC_DS04351,BMG_DS006619,Marchiafava-Bignami Disease
+BMGC_DS04352,BMG_DS006622,Middle Cerebral Artery Syndrome
+BMGC_DS04353,BMG_DS006624,Mucolipidosis Type IV
+BMGC_DS04354,BMG_DS006625,"Muscular Dystrophy, Facioscapulohumeral"
+BMGC_DS04355,BMG_DS006626,Myxedema coma
+BMGC_DS04356,BMG_DS006627,nasopharynx carcinoma
+BMGC_DS04357,BMG_DS006630,Ischemic peripheral neuropathy
+BMGC_DS04358,BMG_DS006632,ovarian germ cell tumor
+BMGC_DS04359,BMG_DS006633,scrotum Paget disease
+BMGC_DS04360,BMG_DS006635,pancreatic cystadenocarcinoma
+BMGC_DS04361,BMG_DS006636,Hereditary pancreatitis
+BMGC_DS04362,BMG_DS006638,squamous cell carcinoma of penis
+BMGC_DS04363,BMG_DS006641,penile sarcoma
+BMGC_DS04364,BMG_DS006643,Hyperkalemic periodic paralysis
+BMGC_DS04365,BMG_DS006644,Hypokalemic periodic paralysis
+BMGC_DS04366,BMG_DS006650,Pneumoconiosis caused by talc
+BMGC_DS04367,BMG_DS006651,Desquamative interstitial pneumonia
+BMGC_DS04368,BMG_DS006652,prostate sarcoma
+BMGC_DS04369,BMG_DS006653,Pycnodysostosis
+BMGC_DS04370,BMG_DS006655,renal pelvis squamous cell carcinoma
+BMGC_DS04371,BMG_DS006659,Selenium deficiency
+BMGC_DS04372,BMG_DS006660,Hemoglobin SS disease with crisis
+BMGC_DS04373,BMG_DS006661,spinal cord ependymoma
+BMGC_DS04374,BMG_DS006662,"Epidural Abscess, Spinal"
+BMGC_DS04375,BMG_DS006667,testicular embryonal carcinoma
+BMGC_DS04376,BMG_DS006668,choriocarcinoma of testis
+BMGC_DS04377,BMG_DS006670,Cavernous Sinus Thrombosis
+BMGC_DS04378,BMG_DS006672,thyroid gland undifferentiated (anaplastic) carcinoma
+BMGC_DS04379,BMG_DS006673,medullary thyroid gland carcinoma
+BMGC_DS04380,BMG_DS006674,thyroid gland papillary carcinoma
+BMGC_DS04381,BMG_DS006677,Transient erythroblastopenia of childhood
+BMGC_DS04382,BMG_DS006678,Prolapse of urethra
+BMGC_DS04383,BMG_DS006679,posterior urethral valve
+BMGC_DS04384,BMG_DS006681,vagina sarcoma
+BMGC_DS04385,BMG_DS006682,vulva sarcoma
+BMGC_DS04386,BMG_DS006683,Infection by Yersinia enterocolitica
+BMGC_DS04387,BMG_DS006684,Acrogeria
+BMGC_DS04388,BMG_DS006685,Aminoaciduria
+BMGC_DS04389,BMG_DS006689,brain hemangioma
+BMGC_DS04390,BMG_DS006695,Conjunctival telangiectasis
+BMGC_DS04391,BMG_DS006697,Candidiasis of the esophagus
+BMGC_DS04392,BMG_DS006705,"Color Blindness, Green"
+BMGC_DS04393,BMG_DS006708,Harlequin Fetus
+BMGC_DS04394,BMG_DS006709,"Fibrosis, Liver"
+BMGC_DS04395,BMG_DS006710,Hypoalbuminemia
+BMGC_DS04396,BMG_DS006711,coloboma of iris
+BMGC_DS04397,BMG_DS006714,larynx squamous papilloma
+BMGC_DS04398,BMG_DS006718,Rotary Nystagmus
+BMGC_DS04399,BMG_DS006723,cerebral lymphoma
+BMGC_DS04400,BMG_DS006725,Rheumatoid Vasculitis
+BMGC_DS04401,BMG_DS006726,congenital vertical talus
+BMGC_DS04402,BMG_DS006727,sensory ataxia
+BMGC_DS04403,BMG_DS006728,"creatine phosphokinase, elevated serum"
+BMGC_DS04404,BMG_DS006730,Superficial ulcer of skin (disorder)
+BMGC_DS04405,BMG_DS006737,adhesions of uterus
+BMGC_DS04406,BMG_DS006744,Cerebrovascular Insufficiency
+BMGC_DS04407,BMG_DS006750,"Hematuria, Benign Familial"
+BMGC_DS04408,BMG_DS006751,Autoimmune Chronic Hepatitis
+BMGC_DS04409,BMG_DS006755,X-linked hypogammaglobulinemia
+BMGC_DS04410,BMG_DS006758,kidney angiomyolipoma
+BMGC_DS04411,BMG_DS006762,vulvar melanoma
+BMGC_DS04412,BMG_DS006765,Sciatic Neuritis
+BMGC_DS04413,BMG_DS006766,"Pancreatitis, Acute Edematous"
+BMGC_DS04414,BMG_DS006770,Pulmonary congestion
+BMGC_DS04415,BMG_DS006773,Thrombotic Stroke
+BMGC_DS04416,BMG_DS006778,Pelvic Inflammatory Disease
+BMGC_DS04417,BMG_DS006779,"Jaundice, Hemolytic"
+BMGC_DS04418,BMG_DS006781,Calcium Pyrophosphate Dihydrate Deposition
+BMGC_DS04419,BMG_DS006782,Color blindness
+BMGC_DS04420,BMG_DS006783,Coronary Stenosis
+BMGC_DS04421,BMG_DS006785,McCune-Albright Syndrome
+BMGC_DS04422,BMG_DS006786,mu-heavy chain disease
+BMGC_DS04423,BMG_DS006789,Dyslipidemias
+BMGC_DS04424,BMG_DS006790,Sexual Infantilism
+BMGC_DS04425,BMG_DS006791,Sheehan Syndrome
+BMGC_DS04426,BMG_DS006792,Panhypopituitarism
+BMGC_DS04427,BMG_DS006793,Erectile dysfunction
+BMGC_DS04428,BMG_DS006794,Congenital Disorders
+BMGC_DS04429,BMG_DS006795,islet cell tumor
+BMGC_DS04430,BMG_DS006796,lung cancer
+BMGC_DS04431,BMG_DS006797,Libman-Sacks Disease
+BMGC_DS04432,BMG_DS006798,Lyme Arthritis
+BMGC_DS04433,BMG_DS006799,Age related macular degeneration
+BMGC_DS04434,BMG_DS006800,Mandibulofacial Dysostosis
+BMGC_DS04435,BMG_DS006803,retinal edema
+BMGC_DS04436,BMG_DS006804,Parkinsonian Disorders
+BMGC_DS04437,BMG_DS006805,Ramsay Hunt Paralysis Syndrome
+BMGC_DS04438,BMG_DS006806,Chylopericardium
+BMGC_DS04439,BMG_DS006807,Simple Pulmonary Eosinophilia
+BMGC_DS04440,BMG_DS006808,"Purpura, Nonthrombocytopenic"
+BMGC_DS04441,BMG_DS006809,Enthesopathy
+BMGC_DS04442,BMG_DS006811,Paroxysmal Reciprocal Tachycardia
+BMGC_DS04443,BMG_DS006813,"Gonadal Dysgenesis, 45,X"
+BMGC_DS04444,BMG_DS006814,Azotemia
+BMGC_DS04445,BMG_DS006817,Opsoclonus
+BMGC_DS04446,BMG_DS006818,Bare Lymphocyte Syndrome
+BMGC_DS04447,BMG_DS006819,Autoimmune thrombocytopenia
+BMGC_DS04448,BMG_DS006820,Leukocyte-Adhesion Deficiency Syndrome
+BMGC_DS04449,BMG_DS006823,Brown-Sequard Syndrome
+BMGC_DS04450,BMG_DS006824,Blue Toe Syndrome
+BMGC_DS04451,BMG_DS006825,MALT lymphoma
+BMGC_DS04452,BMG_DS006826,Protein S Deficiency
+BMGC_DS04453,BMG_DS006830,"Bone Demineralization, Pathologic"
+BMGC_DS04454,BMG_DS006831,Space Motion Sickness
+BMGC_DS04455,BMG_DS006833,Bronchiolitis Obliterans Organizing Pneumonia
+BMGC_DS04456,BMG_DS006834,male breast cancer
+BMGC_DS04457,BMG_DS006836,Proliferative vitreoretinopathy
+BMGC_DS04458,BMG_DS006837,Congenital atresia of pulmonary valve
+BMGC_DS04459,BMG_DS006841,Systemic Inflammatory Response Syndrome
+BMGC_DS04460,BMG_DS006842,Multiple Chemical Sensitivity
+BMGC_DS04461,BMG_DS006848,Abdominal Abscess
+BMGC_DS04462,BMG_DS006849,tricuspid atresia
+BMGC_DS04463,BMG_DS006850,Viral Encephalitis
+BMGC_DS04464,BMG_DS006851,Hantavirus Pulmonary Syndrome
+BMGC_DS04465,BMG_DS006852,Sepsis
+BMGC_DS04466,BMG_DS006855,Autonomic neuropathy
+BMGC_DS04467,BMG_DS006857,sebocystomatosis
+BMGC_DS04468,BMG_DS006860,fibrous dysplasia
+BMGC_DS04469,BMG_DS006861,telangiectatic osteogenic sarcoma
+BMGC_DS04470,BMG_DS006862,mixed glioma
+BMGC_DS04471,BMG_DS006864,rhabdoid meningioma
+BMGC_DS04472,BMG_DS006866,Punctate keratitis
+BMGC_DS04473,BMG_DS006867,Purulent endophthalmitis
+BMGC_DS04474,BMG_DS006870,hearing disorder
+BMGC_DS04475,BMG_DS006874,carcinoma of the ampulla of vater
+BMGC_DS04476,BMG_DS006879,"Cardiac valvular dysplasia, X-linked"
+BMGC_DS04477,BMG_DS006887,Anterolateral Myocardial Infarction
+BMGC_DS04478,BMG_DS006888,Anteroseptal Myocardial Infarction
+BMGC_DS04479,BMG_DS006891,lung oat cell carcinoma
+BMGC_DS04480,BMG_DS006894,parathyroid gland adenoma
+BMGC_DS04481,BMG_DS006899,Recurrent urinary tract infection
+BMGC_DS04482,BMG_DS006903,extragonadal germ cell tumor
+BMGC_DS04483,BMG_DS006915,Spongiotic dermatitis
+BMGC_DS04484,BMG_DS006916,Psoriasiform eczema
+BMGC_DS04485,BMG_DS006919,Cutaneous Vasculitis
+BMGC_DS04486,BMG_DS007190,Contact dermatitis caused by urushiol from Pacific poison oak
+BMGC_DS04487,BMG_DS007207,Pemphigus Foliaceus
+BMGC_DS04488,BMG_DS007220,"Urticaria, Aquagenic"
+BMGC_DS04489,BMG_DS007224,Chronic Urticaria
+BMGC_DS04490,BMG_DS007237,Prurigo nodularis
+BMGC_DS04491,BMG_DS007251,Gianotti-Crosti Syndrome
+BMGC_DS04492,BMG_DS007255,Distinctive exudative discoid AND lichenoid chronic dermatosis of Sulzberger and Garbe
+BMGC_DS04493,BMG_DS007260,Kyrle disease
+BMGC_DS04494,BMG_DS007261,Keratosis pilaris
+BMGC_DS04495,BMG_DS007262,"papillomatosis, confluent and reticulated"
+BMGC_DS04496,BMG_DS007272,Erythema elevatum diutinum
+BMGC_DS04497,BMG_DS007275,Cutis marmorata
+BMGC_DS04498,BMG_DS007276,Telangiectasia macularis eruptiva perstans
+BMGC_DS04499,BMG_DS007279,Linear Scleroderma
+BMGC_DS04500,BMG_DS007285,Hyperkeratosis lenticularis perstans
+BMGC_DS04501,BMG_DS007290,Burnett Schwartz Berberian syndrome
+BMGC_DS04502,BMG_DS007291,Atrophoderma vermiculatum
+BMGC_DS04503,BMG_DS007311,Chloracne
+BMGC_DS04504,BMG_DS007323,Miliaria profunda
+BMGC_DS04505,BMG_DS007325,Granulosis Rubra Nasi
+BMGC_DS04506,BMG_DS007331,Diffuse alopecia areata
+BMGC_DS04507,BMG_DS007338,Pili annulati
+BMGC_DS04508,BMG_DS007340,pili torti
+BMGC_DS04509,BMG_DS007351,Alopecia universalis
+BMGC_DS04510,BMG_DS007352,Perifolliculitis capitis abscedens
+BMGC_DS04511,BMG_DS007362,Telogen effluvium
+BMGC_DS04512,BMG_DS007406,Drug-induced lupus erythematosus
+BMGC_DS04513,BMG_DS007437,angioma serpiginosum
+BMGC_DS04514,BMG_DS007438,Angiokeratoma circumscriptum
+BMGC_DS04515,BMG_DS007439,angiokeratoma of Fordyce
+BMGC_DS04516,BMG_DS007440,angiokeratoma of mibelli
+BMGC_DS04517,BMG_DS007458,Disseminated eosinophilic collagen disease
+BMGC_DS04518,BMG_DS007462,"Dermatomyositis, Childhood Type"
+BMGC_DS04519,BMG_DS007583,SAPHO syndrome
+BMGC_DS04520,BMG_DS007611,Capsulitis
+BMGC_DS04521,BMG_DS007635,Achilles tendinitis
+BMGC_DS04522,BMG_DS007658,Olecranon bursitis
+BMGC_DS04523,BMG_DS007668,Polymyositis Ossificans
+BMGC_DS04524,BMG_DS007680,Knuckle pads
+BMGC_DS04525,BMG_DS007684,Eosinophilic Fasciitis
+BMGC_DS04526,BMG_DS007687,Hepatic osteodystrophy
+BMGC_DS04527,BMG_DS007748,Osteoarthropathy of fingers familial
+BMGC_DS04528,BMG_DS007771,drug-induced osteoporosis
+BMGC_DS04529,BMG_DS007775,"Atrophy, Disuse"
+BMGC_DS04530,BMG_DS007782,idiopathic camptocormia
+BMGC_DS04531,BMG_DS007815,Chronic disease of respiratory system
+BMGC_DS04532,BMG_DS007878,congenital laryngomalacia
+BMGC_DS04533,BMG_DS007892,Calcification of trachea
+BMGC_DS04534,BMG_DS007909,Bronchomalacia
+BMGC_DS04535,BMG_DS007912,Cylindrical Bronchiectasis
+BMGC_DS04536,BMG_DS007914,Saccular Bronchiectasis
+BMGC_DS04537,BMG_DS007944,Panacinar Emphysema
+BMGC_DS04538,BMG_DS007964,"Asthma, Occupational"
+BMGC_DS04539,BMG_DS007973,Kaolinosis
+BMGC_DS04540,BMG_DS008010,Acute respiratory failure
+BMGC_DS04541,BMG_DS008019,Compression Pulmonary Atelectasis
+BMGC_DS04542,BMG_DS008027,Endogenous Lipid Pneumonia
+BMGC_DS04543,BMG_DS008028,Lymphoid interstitial pneumonia
+BMGC_DS04544,BMG_DS008031,"Pneumonia, Necrotizing"
+BMGC_DS04545,BMG_DS008069,Tension Pneumothorax
+BMGC_DS04546,BMG_DS008089,Spastic Dysphonia
+BMGC_DS04547,BMG_DS008099,"Voice Disorder, Neurologic"
+BMGC_DS04548,BMG_DS008106,Apraxia of Phonation
+BMGC_DS04549,BMG_DS008167,Chronic myocardial ischemia
+BMGC_DS04550,BMG_DS008181,Acute heart failure
+BMGC_DS04551,BMG_DS008183,Chronic heart failure
+BMGC_DS04552,BMG_DS008207,Rheumatic fever without heart involvement
+BMGC_DS04553,BMG_DS008209,Chorea Gravidarum
+BMGC_DS04554,BMG_DS008226,Rheumatic disease of mitral valve
+BMGC_DS04555,BMG_DS008234,Mitral and aortic incompetence
+BMGC_DS04556,BMG_DS008236,Rheumatic tricuspid valve disease
+BMGC_DS04557,BMG_DS008247,Familial cardiomyopathy
+BMGC_DS04558,BMG_DS008285,Primary eosinophilic endomyocardial restrictive cardiomyopathy
+BMGC_DS04559,BMG_DS008330,Myxoid transformation of mitral valve
+BMGC_DS04560,BMG_DS008331,Conduction disorder of the heart
+BMGC_DS04561,BMG_DS008336,Nodal rhythm disorder
+BMGC_DS04562,BMG_DS008342,Second degree atrioventricular block
+BMGC_DS04563,BMG_DS008370,Systemic Vasculitis
+BMGC_DS04564,BMG_DS008409,Ruptured thoracic aortic aneurysm
+BMGC_DS04565,BMG_DS008410,Ruptured abdominal aortic aneurysm
+BMGC_DS04566,BMG_DS008419,Portal vein obstruction
+BMGC_DS04567,BMG_DS008437,Thrombophlebitis of superficial veins of lower extremity
+BMGC_DS04568,BMG_DS008445,Thrombophlebitis of the femoral vein
+BMGC_DS04569,BMG_DS008462,Basilar Artery Stenosis
+BMGC_DS04570,BMG_DS008463,basilar artery occlusion
+BMGC_DS04571,BMG_DS008465,Carotid artery occlusion
+BMGC_DS04572,BMG_DS008466,Vertebral Artery Stenosis
+BMGC_DS04573,BMG_DS008470,Cerebral Vasospasm
+BMGC_DS04574,BMG_DS008475,Acute cerebrovascular insufficiency
+BMGC_DS04575,BMG_DS008543,De Sanctis-Cacchione syndrome
+BMGC_DS04576,BMG_DS008544,Seckel syndrome
+BMGC_DS04577,BMG_DS008546,Robinow Syndrome
+BMGC_DS04578,BMG_DS008551,Weaver syndrome
+BMGC_DS04579,BMG_DS008552,Marshall-Smith syndrome
+BMGC_DS04580,BMG_DS008554,Distal arthrogryposis syndrome
+BMGC_DS04581,BMG_DS008556,Meckel-Gruber syndrome
+BMGC_DS04582,BMG_DS008557,X-linked hydrocephalus syndrome
+BMGC_DS04583,BMG_DS008559,Miller Dieker syndrome
+BMGC_DS04584,BMG_DS008560,Pallister-Hall syndrome
+BMGC_DS04585,BMG_DS008561,Walker-Warburg congenital muscular dystrophy
+BMGC_DS04586,BMG_DS008562,Royer Syndrome
+BMGC_DS04587,BMG_DS008563,Cohen syndrome
+BMGC_DS04588,BMG_DS008564,Freeman-Sheldon syndrome
+BMGC_DS04589,BMG_DS008565,Hecht syndrome (disorder)
+BMGC_DS04590,BMG_DS008566,Schinzel-Giedion syndrome
+BMGC_DS04591,BMG_DS008570,Cryptophthalmos syndrome
+BMGC_DS04592,BMG_DS008571,Branchio-Oto-Renal Syndrome
+BMGC_DS04593,BMG_DS008572,Marshall syndrome
+BMGC_DS04594,BMG_DS008574,Wildervanck's syndrome
+BMGC_DS04595,BMG_DS008575,Goldenhar Syndrome
+BMGC_DS04596,BMG_DS008577,agnathia-otocephaly complex
+BMGC_DS04597,BMG_DS008579,Nager syndrome
+BMGC_DS04598,BMG_DS008580,Townes syndrome
+BMGC_DS04599,BMG_DS008581,Ruvalcaba Syndrome
+BMGC_DS04600,BMG_DS008582,Mental retardation Mietens Weber type
+BMGC_DS04601,BMG_DS008583,Oto-Palato-digital syndrome type 1
+BMGC_DS04602,BMG_DS008584,Coffin-Lowry syndrome
+BMGC_DS04603,BMG_DS008585,Stickler syndrome (disorder)
+BMGC_DS04604,BMG_DS008586,Trichorhinophalangeal syndrome
+BMGC_DS04605,BMG_DS008587,Genee-Wiedemann syndrome
+BMGC_DS04606,BMG_DS008589,Popliteal pterygium syndrome
+BMGC_DS04607,BMG_DS008590,"Chondrodysplasia, Grebe type"
+BMGC_DS04608,BMG_DS008591,autosomal recessive multiple pterygium syndrome
+BMGC_DS04609,BMG_DS008593,Femoral hypoplasia - unusual facies syndrome
+BMGC_DS04610,BMG_DS008594,Holt-Oram syndrome
+BMGC_DS04611,BMG_DS008595,Aase syndrome
+BMGC_DS04612,BMG_DS008596,Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects
+BMGC_DS04613,BMG_DS008597,Adams-Oliver syndrome
+BMGC_DS04614,BMG_DS008598,Lacrimoauriculodentodigital syndrome
+BMGC_DS04615,BMG_DS008599,achondrogenesis type IA
+BMGC_DS04616,BMG_DS008600,achondrogenesis type IB
+BMGC_DS04617,BMG_DS008601,Jeune thoracic dystrophy
+BMGC_DS04618,BMG_DS008602,Kniest dysplasia
+BMGC_DS04619,BMG_DS008603,"Spondylometaphyseal dysplasia, Kozlowski type"
+BMGC_DS04620,BMG_DS008604,metatropic dysplasia
+BMGC_DS04621,BMG_DS008605,fibrochondrogenesis
+BMGC_DS04622,BMG_DS008606,atelosteogenesis type I
+BMGC_DS04623,BMG_DS008607,Dyggve-Melchior-Clausen syndrome
+BMGC_DS04624,BMG_DS008608,Acromicric dysplasia
+BMGC_DS04625,BMG_DS008609,Metaphyseal chondrodysplasia Schmid type
+BMGC_DS04626,BMG_DS008610,metaphyseal chondrodysplasia
+BMGC_DS04627,BMG_DS008612,craniometaphyseal dysplasia
+BMGC_DS04628,BMG_DS008613,frontometaphyseal dysplasia
+BMGC_DS04629,BMG_DS008614,Pyle metaphyseal dysplasia
+BMGC_DS04630,BMG_DS008615,Jansen type metaphyseal chondrodysplasia
+BMGC_DS04631,BMG_DS008619,Sclerosteosis
+BMGC_DS04632,BMG_DS008621,Greig cephalopolysyndactyly syndrome
+BMGC_DS04633,BMG_DS008622,Baller-Gerold syndrome
+BMGC_DS04634,BMG_DS008623,Leri-Weill dyschondrosteosis
+BMGC_DS04635,BMG_DS008626,Weill-Marchesani syndrome
+BMGC_DS04636,BMG_DS008628,Neurocutaneous Syndromes
+BMGC_DS04637,BMG_DS008631,Peutz-Jeghers syndrome
+BMGC_DS04638,BMG_DS008633,Bannayan-Riley-Ruvalcaba Syndrome
+BMGC_DS04639,BMG_DS008635,Organoid Nevus Phakomatosis
+BMGC_DS04640,BMG_DS008636,Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)
+BMGC_DS04641,BMG_DS008637,Tricho-dento-osseous syndrome (disorder)
+BMGC_DS04642,BMG_DS008638,Pachyonychia Congenita
+BMGC_DS04643,BMG_DS008640,Senter syndrome
+BMGC_DS04644,BMG_DS008641,Coffin-Siris syndrome
+BMGC_DS04645,BMG_DS008642,Borjeson-Forssman-Lehmann syndrome
+BMGC_DS04646,BMG_DS008643,Rieger syndrome
+BMGC_DS04647,BMG_DS008644,Cerebrocostomandibular Syndrome
+BMGC_DS04648,BMG_DS008645,Jarcho-Levin syndrome
+BMGC_DS04649,BMG_DS008646,Donohue Syndrome
+BMGC_DS04650,BMG_DS008647,Lymphedema distichiasis syndrome
+BMGC_DS04651,BMG_DS008653,CHARGE Syndrome
+BMGC_DS04652,BMG_DS008663,Warfarin syndrome
+BMGC_DS04653,BMG_DS008724,Pallister-Killian syndrome
+BMGC_DS04654,BMG_DS008757,ring chromosome 20
+BMGC_DS04655,BMG_DS008768,Cat eye syndrome
+BMGC_DS04656,BMG_DS008774,"49,XXXXY Syndrome"
+BMGC_DS04657,BMG_DS008778,Dermatofibrosis lenticularis disseminata
+BMGC_DS04658,BMG_DS008779,trigonocephaly
+BMGC_DS04659,BMG_DS008780,megalodactyly
+BMGC_DS04660,BMG_DS008781,split hand-foot malformation
+BMGC_DS04661,BMG_DS008782,acheiropody
+BMGC_DS04662,BMG_DS008783,congenital elbow dislocation
+BMGC_DS04663,BMG_DS008784,congenital shoulder dislocation
+BMGC_DS04664,BMG_DS008790,radial hemimelia
+BMGC_DS04665,BMG_DS008798,familial isolated clinodactyly of fingers
+BMGC_DS04666,BMG_DS008803,tibial hemimelia
+BMGC_DS04667,BMG_DS008812,Gastroschisis
+BMGC_DS04668,BMG_DS008816,larynx atresia
+BMGC_DS04669,BMG_DS008819,pulmonary agenesis
+BMGC_DS04670,BMG_DS008820,pulmonary hypoplasia
+BMGC_DS04671,BMG_DS008822,congenital lobar emphysema
+BMGC_DS04672,BMG_DS008829,aortic valve atresia
+BMGC_DS04673,BMG_DS008836,Uhl anomaly
+BMGC_DS04674,BMG_DS008853,Erythrokeratodermia variabilis
+BMGC_DS04675,BMG_DS008854,Ichthyosis linearis circumflexa
+BMGC_DS04676,BMG_DS008855,keratoderma hereditarium mutilans
+BMGC_DS04677,BMG_DS008856,Dyskeratosis Congenita
+BMGC_DS04678,BMG_DS008857,Hereditary benign intraepithelial dyskeratosis
+BMGC_DS04679,BMG_DS008858,"Porokeratosis, Disseminated Superficial Actinic"
+BMGC_DS04680,BMG_DS008859,Acrokeratosis Verruciformis of Hopf
+BMGC_DS04681,BMG_DS008862,mongolian spot
+BMGC_DS04682,BMG_DS008863,nevus comedonicus syndrome
+BMGC_DS04683,BMG_DS008867,nonsyndromic congenital nail disorder 4
+BMGC_DS04684,BMG_DS008868,nonsyndromic congenital nail disorder 2
+BMGC_DS04685,BMG_DS008869,"Knuckle pads, leuconychia and sensorineural deafness"
+BMGC_DS04686,BMG_DS008870,Pili torti-deafness syndrome
+BMGC_DS04687,BMG_DS008872,familial supernumerary nipples
+BMGC_DS04688,BMG_DS008875,Paramolar tubercle of bolk
+BMGC_DS04689,BMG_DS008877,Taurodontism
+BMGC_DS04690,BMG_DS008889,pyloric atresia
+BMGC_DS04691,BMG_DS008890,atresia of small intestine
+BMGC_DS04692,BMG_DS008891,duodenal atresia
+BMGC_DS04693,BMG_DS008897,isolated agenesis of gallbladder
+BMGC_DS04694,BMG_DS008900,thyroid ectopia
+BMGC_DS04695,BMG_DS008901,"renal agenesis, unilateral"
+BMGC_DS04696,BMG_DS008902,renal hypoplasia
+BMGC_DS04697,BMG_DS008903,Allanson Pantzar McLeod syndrome
+BMGC_DS04698,BMG_DS008909,"Hermaphroditism, True"
+BMGC_DS04699,BMG_DS008910,uterine anomalies
+BMGC_DS04700,BMG_DS008917,Testicular regression syndrome
+BMGC_DS04701,BMG_DS008918,"Leydig cell hypoplasia, type 1"
+BMGC_DS04702,BMG_DS008920,lissencephaly spectrum disorders
+BMGC_DS04703,BMG_DS008921,polymicrogyria
+BMGC_DS04704,BMG_DS008922,pontocerebellar hypoplasia
+BMGC_DS04705,BMG_DS008924,lissencephaly
+BMGC_DS04706,BMG_DS008925,schizencephaly
+BMGC_DS04707,BMG_DS008926,Etat Marbre
+BMGC_DS04708,BMG_DS008928,Neuronal heterotopia
+BMGC_DS04709,BMG_DS008932,Marcus Gunn phenomenon
+BMGC_DS04710,BMG_DS008933,Norrie disease
+BMGC_DS04711,BMG_DS008936,cataract 5 multiple types
+BMGC_DS04712,BMG_DS008937,total early-onset cataract
+BMGC_DS04713,BMG_DS008938,Axenfeld anomaly
+BMGC_DS04714,BMG_DS008939,persistent hyperplastic primary vitreous
+BMGC_DS04715,BMG_DS008940,congenital ptosis
+BMGC_DS04716,BMG_DS008944,ear malformation
+BMGC_DS04717,BMG_DS008947,holoprosencephaly 1
+BMGC_DS04718,BMG_DS008957,Compression of umbilical cord
+BMGC_DS04719,BMG_DS008976,"Visceral Myopathy, Familial"
+BMGC_DS04720,BMG_DS008981,Dental caries extending into dentin
+BMGC_DS04721,BMG_DS008985,Enamel caries
+BMGC_DS04722,BMG_DS009004,External resorption of tooth
+BMGC_DS04723,BMG_DS009018,Periapical abscess with sinus
+BMGC_DS04724,BMG_DS009022,Localized gingival recession
+BMGC_DS04725,BMG_DS009025,Epulides
+BMGC_DS04726,BMG_DS009033,Chronic Periodontitis
+BMGC_DS04727,BMG_DS009077,Benign lymphoepithelial lesion of salivary gland
+BMGC_DS04728,BMG_DS009080,Vesicular Stomatitis
+BMGC_DS04729,BMG_DS009095,Actinic cheilitis
+BMGC_DS04730,BMG_DS009114,Erosive esophagitis
+BMGC_DS04731,BMG_DS009126,Oropharyngeal Dysphagia
+BMGC_DS04732,BMG_DS009127,Esophageal Dysphagia
+BMGC_DS04733,BMG_DS009136,esophageal leukoplakia
+BMGC_DS04734,BMG_DS009146,Acute gastric mucosal erosion
+BMGC_DS04735,BMG_DS009184,Eosinophilic gastritis
+BMGC_DS04736,BMG_DS009203,Gastroparesis due to diabetes mellitus
+BMGC_DS04737,BMG_DS009207,Cascade stomach
+BMGC_DS04738,BMG_DS009227,Gastric Antral Vascular Ectasia
+BMGC_DS04739,BMG_DS009295,Acute peptic ulcer with hemorrhage
+BMGC_DS04740,BMG_DS009344,Angiodysplasia of intestine
+BMGC_DS04741,BMG_DS009350,Chronic colitis
+BMGC_DS04742,BMG_DS009360,Severe chronic ulcerative colitis
+BMGC_DS04743,BMG_DS009363,Chronic ulcerative rectosigmoiditis
+BMGC_DS04744,BMG_DS009405,Non-infective diarrhea
+BMGC_DS04745,BMG_DS009427,Stenosis of intestine
+BMGC_DS04746,BMG_DS009444,Ulceration of colon
+BMGC_DS04747,BMG_DS009450,Meckel's diverticulitis
+BMGC_DS04748,BMG_DS009455,Diverticulitis of small intestine
+BMGC_DS04749,BMG_DS009461,Chronic idiopathic constipation
+BMGC_DS04750,BMG_DS009504,Drug and toxin-induced diarrhea
+BMGC_DS04751,BMG_DS009580,Congenital chloride diarrhea
+BMGC_DS04752,BMG_DS009581,"Congenital secretory diarrhea, sodium type (disorder)"
+BMGC_DS04753,BMG_DS009603,Paraesophageal hernia
+BMGC_DS04754,BMG_DS009647,Hepatobiliary Disorder
+BMGC_DS04755,BMG_DS009652,Acute hepatitis
+BMGC_DS04756,BMG_DS009664,"Cirrhosis, Cryptogenic"
+BMGC_DS04757,BMG_DS009682,Liver cyst
+BMGC_DS04758,BMG_DS009687,Acalculous Cholecystitis
+BMGC_DS04759,BMG_DS009748,Acute cholangitis
+BMGC_DS04760,BMG_DS009749,Chronic cholangitis
+BMGC_DS04761,BMG_DS009750,Primary cholangitis
+BMGC_DS04762,BMG_DS009754,Suppurative cholangitis
+BMGC_DS04763,BMG_DS009765,"Pancreatitis, Acute Hemorrhagic"
+BMGC_DS04764,BMG_DS009766,Pancreatitis Necrotizing
+BMGC_DS04765,BMG_DS009777,Peripancreatic Fat Necrosis
+BMGC_DS04766,BMG_DS009784,Exocrine pancreatic insufficiency
+BMGC_DS04767,BMG_DS009823,Disorder of acid-base balance
+BMGC_DS04768,BMG_DS009850,Neonatal hemochromatosis
+BMGC_DS04769,BMG_DS009851,Juvenile hemochromatosis
+BMGC_DS04770,BMG_DS009861,Hypocupremia
+BMGC_DS04771,BMG_DS009869,"Hypercalcemia, Idiopathic, of Infancy"
+BMGC_DS04772,BMG_DS009878,Keshan disease
+BMGC_DS04773,BMG_DS009887,Chronic gouty arthritis
+BMGC_DS04774,BMG_DS009895,"Gout, HPRT-Related"
+BMGC_DS04775,BMG_DS009896,"Xanthinuria, Type I"
+BMGC_DS04776,BMG_DS009897,Combined molybdoflavoprotein enzyme deficiency
+BMGC_DS04777,BMG_DS009898,Adenine phosphoribosyltransferase deficiency
+BMGC_DS04778,BMG_DS009899,"APRT deficiency, Japanese type"
+BMGC_DS04779,BMG_DS009902,Adenosine deaminase deficiency
+BMGC_DS04780,BMG_DS009903,Purine-nucleoside phosphorylase deficiency
+BMGC_DS04781,BMG_DS009904,Adenylosuccinate lyase deficiency (disorder)
+BMGC_DS04782,BMG_DS009907,"Hereditary orotic aciduria, type 1"
+BMGC_DS04783,BMG_DS009910,"Xeroderma pigmentosum, group A"
+BMGC_DS04784,BMG_DS009911,"Xeroderma pigmentosum, group B"
+BMGC_DS04785,BMG_DS009912,"Xeroderma Pigmentosum, Complementation Group D"
+BMGC_DS04786,BMG_DS009913,xeroderma pigmentosum group F
+BMGC_DS04787,BMG_DS009914,"Xeroderma pigmentosum, group G"
+BMGC_DS04788,BMG_DS009918,Glucose-6-phosphate transport defect
+BMGC_DS04789,BMG_DS009919,"Glycogen storage disease, type IX"
+BMGC_DS04790,BMG_DS009921,Glycogen storage disease type X
+BMGC_DS04791,BMG_DS009922,Classical galactosemia
+BMGC_DS04792,BMG_DS009923,"Classical galactosemia, homozygous Duarte-type"
+BMGC_DS04793,BMG_DS009926,Deficiency of galactokinase
+BMGC_DS04794,BMG_DS009928,Deficiency of fructokinase
+BMGC_DS04795,BMG_DS009930,Pentosuria
+BMGC_DS04796,BMG_DS009932,"Primary hyperoxaluria, type I"
+BMGC_DS04797,BMG_DS009933,Primary hyperoxaluria type 2
+BMGC_DS04798,BMG_DS009944,"Lactase Deficiency, Congenital"
+BMGC_DS04799,BMG_DS009946,"Lactose Intolerance, Adult Type"
+BMGC_DS04800,BMG_DS009950,Congenital glucose-galactose malabsorption
+BMGC_DS04801,BMG_DS009951,"alpha, alpha-Trehalase deficiency"
+BMGC_DS04802,BMG_DS009957,NADH cytochrome B5 reductase deficiency
+BMGC_DS04803,BMG_DS009958,Phosphoenolpyruvate carboxykinase deficiency
+BMGC_DS04804,BMG_DS009962,Familial apolipoprotein C-II deficiency
+BMGC_DS04805,BMG_DS009972,Fucosidosis Type I
+BMGC_DS04806,BMG_DS009973,Fucosidosis Type II
+BMGC_DS04807,BMG_DS009974,Aspartylglucosaminuria
+BMGC_DS04808,BMG_DS009975,Type I Mucolipidosis
+BMGC_DS04809,BMG_DS009976,Neuraminidase 1 deficiency
+BMGC_DS04810,BMG_DS009981,GALACTOSIALIDOSIS
+BMGC_DS04811,BMG_DS009982,Cytochrome-c Oxidase Deficiency
+BMGC_DS04812,BMG_DS009983,Triglyceride storage disease with ichthyosis
+BMGC_DS04813,BMG_DS009986,"Niemann-Pick Disease, Type A"
+BMGC_DS04814,BMG_DS009987,"Niemann-Pick Disease, Type B"
+BMGC_DS04815,BMG_DS009991,"Niemann-Pick Disease, Type D"
+BMGC_DS04816,BMG_DS009992,"Niemann-Pick Disease, Type E"
+BMGC_DS04817,BMG_DS009993,"Gaucher Disease, Type 2"
+BMGC_DS04818,BMG_DS009994,"Gaucher Disease, Type 3"
+BMGC_DS04819,BMG_DS009995,Late-Onset Globoid Cell Leukodystrophy
+BMGC_DS04820,BMG_DS009996,Farber Lipogranulomatosis
+BMGC_DS04821,BMG_DS009999,Metachromatic Leukodystrophy due to Saposin B Deficiency
+BMGC_DS04822,BMG_DS010000,Multiple Sulfatase Deficiency Disease
+BMGC_DS04823,BMG_DS010001,"Gangliosidosis, Generalized GM1, Type 1"
+BMGC_DS04824,BMG_DS010002,"Gangliosidosis, Generalized GM1, Type 2"
+BMGC_DS04825,BMG_DS010003,"Gangliosidosis, Generalized GM1, Type 3"
+BMGC_DS04826,BMG_DS010004,"Gangliosidoses, GM2"
+BMGC_DS04827,BMG_DS010005,"Tay-Sachs Disease, AB Variant"
+BMGC_DS04828,BMG_DS010006,Juvenile GM2 gangliosidosis
+BMGC_DS04829,BMG_DS010013,"Adrenal hyperplasia, congenital, type 5"
+BMGC_DS04830,BMG_DS010018,Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency
+BMGC_DS04831,BMG_DS010019,corticosterone methyloxidase type 1 deficiency
+BMGC_DS04832,BMG_DS010020,17-Hydroxysteroid Dehydrogenase Deficiency
+BMGC_DS04833,BMG_DS010021,Pseudovaginal Perineoscrotal Hypospadias
+BMGC_DS04834,BMG_DS010022,Reifenstein Syndrome
+BMGC_DS04835,BMG_DS010030,Progressive intrahepatic cholestasis (disorder)
+BMGC_DS04836,BMG_DS010032,"Cholestasis-edema syndrome, Norwegian type"
+BMGC_DS04837,BMG_DS010035,Cholestasis of pregnancy
+BMGC_DS04838,BMG_DS010039,Familial porphyria cutanea tarda
+BMGC_DS04839,BMG_DS010043,Porphobilinogen synthase deficiency
+BMGC_DS04840,BMG_DS010046,Ehlers-Danlos syndrome type 1
+BMGC_DS04841,BMG_DS010047,Ehlers-Danlos syndrome type 2
+BMGC_DS04842,BMG_DS010048,"Ehlers-Danlos syndrome, type 3 (disorder)"
+BMGC_DS04843,BMG_DS010049,"Ehlers-Danlos Syndrome, Type IV"
+BMGC_DS04844,BMG_DS010050,"autosomal dominant Ehlers-Danlos syndrome, vascular type"
+BMGC_DS04845,BMG_DS010051,"autosomal recessive Ehlers-Danlos syndrome, vascular type"
+BMGC_DS04846,BMG_DS010052,Ehlers-Danlos syndrome type 5
+BMGC_DS04847,BMG_DS010053,Ehlers-Danlos syndrome type 6
+BMGC_DS04848,BMG_DS010055,Ehlers-Danlos syndrome 6B
+BMGC_DS04849,BMG_DS010057,"Ehlers-Danlos Syndrome, Type VIII"
+BMGC_DS04850,BMG_DS010060,"Cutis Laxa, Autosomal Dominant"
+BMGC_DS04851,BMG_DS010061,autosomal recessive cutis laxa type 1
+BMGC_DS04852,BMG_DS010063,occipital horn syndrome
+BMGC_DS04853,BMG_DS010064,De Barsy syndrome
+BMGC_DS04854,BMG_DS010065,"Cutis Laxa, Autosomal Recessive, Type IIA"
+BMGC_DS04855,BMG_DS010068,"Osteogenesis imperfecta, dominant perinatal lethal"
+BMGC_DS04856,BMG_DS010071,Osteogenesis imperfecta type III (disorder)
+BMGC_DS04857,BMG_DS010072,Osteogenesis imperfecta type IV (disorder)
+BMGC_DS04858,BMG_DS010075,epidermolysis bullosa dystrophica Neurotrophica
+BMGC_DS04859,BMG_DS010076,epidermolysis bullosa with congenital localized absence of skin and deformity of nails
+BMGC_DS04860,BMG_DS010078,Adult junctional epidermolysis bullosa (disorder)
+BMGC_DS04861,BMG_DS010081,Pseudocholinesterase deficiency
+BMGC_DS04862,BMG_DS010083,Primary amyloidosis
+BMGC_DS04863,BMG_DS010086,"Familial Amyloid Neuropathy, Portuguese Type"
+BMGC_DS04864,BMG_DS010087,"Familial Amyloid Polyneuropathy, Jewish Type"
+BMGC_DS04865,BMG_DS010088,"Amyloid Polyneuropathy, Swiss Type"
+BMGC_DS04866,BMG_DS010089,"Amyloidosis, familial visceral"
+BMGC_DS04867,BMG_DS010090,Muckle-Wells Syndrome
+BMGC_DS04868,BMG_DS010092,Familial Cerebral Amyloid Angiopathy
+BMGC_DS04869,BMG_DS010094,Primary localized cutaneous amyloidosis
+BMGC_DS04870,BMG_DS010096,"Amyloidosis, Cutaneous Bullous"
+BMGC_DS04871,BMG_DS010102,Hemodialysis-associated amyloidosis
+BMGC_DS04872,BMG_DS010104,Senile cardiac amyloidosis
+BMGC_DS04873,BMG_DS010107,Acid Phosphatase Deficiency
+BMGC_DS04874,BMG_DS010108,Infantile hypophosphatasia
+BMGC_DS04875,BMG_DS010109,Adult hypophosphatasia
+BMGC_DS04876,BMG_DS010110,Hyperphosphatasemia with bone disease
+BMGC_DS04877,BMG_DS010111,Enterokinase Deficiency
+BMGC_DS04878,BMG_DS010112,Pancreatic trypsinogen deficiency
+BMGC_DS04879,BMG_DS010113,Deficiency of glycerol kinase
+BMGC_DS04880,BMG_DS010114,Acatalasia
+BMGC_DS04881,BMG_DS010117,Ethanolaminosis
+BMGC_DS04882,BMG_DS010119,Alstrom Syndrome
+BMGC_DS04883,BMG_DS010127,"Renal Tubular Acidosis, Type II"
+BMGC_DS04884,BMG_DS010128,"Pseudohypoaldosteronism, Type I"
+BMGC_DS04885,BMG_DS010132,Acquired Nephrogenic Diabetes Insipidus
+BMGC_DS04886,BMG_DS010133,"Hypokalemia, Familial"
+BMGC_DS04887,BMG_DS010135,Thyrotoxic periodic paralysis
+BMGC_DS04888,BMG_DS010137,Primary hypomagnesemia (disorder)
+BMGC_DS04889,BMG_DS010139,Gitelman Syndrome
+BMGC_DS04890,BMG_DS010148,Phenylketonuria II
+BMGC_DS04891,BMG_DS010149,"Hyperphenylalaninemia, BH4-Deficient, B"
+BMGC_DS04892,BMG_DS010150,"Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency"
+BMGC_DS04893,BMG_DS010153,Tryptophanuria With Dwarfism
+BMGC_DS04894,BMG_DS010154,Hydroxykynureninuria
+BMGC_DS04895,BMG_DS010156,Blue diaper syndrome
+BMGC_DS04896,BMG_DS010157,Hooft disease
+BMGC_DS04897,BMG_DS010159,tyrosinemia
+BMGC_DS04898,BMG_DS010160,Tyrosinosis
+BMGC_DS04899,BMG_DS010163,Tyrosine Transaminase Deficiency Disease
+BMGC_DS04900,BMG_DS010165,"Tyrosinemia, Type I"
+BMGC_DS04901,BMG_DS010168,Oculocutaneous albinism type 1
+BMGC_DS04902,BMG_DS010169,Oculocutaneous albinism type 2
+BMGC_DS04903,BMG_DS010174,"Ocular albinism, type II"
+BMGC_DS04904,BMG_DS010179,Disorder of histidine metabolism
+BMGC_DS04905,BMG_DS010181,Urocanase deficiency
+BMGC_DS04906,BMG_DS010188,Glutamate-cysteine ligase deficiency
+BMGC_DS04907,BMG_DS010189,gamma-Glutamyltransferase deficiency
+BMGC_DS04908,BMG_DS010190,5-oxoprolinase deficiency
+BMGC_DS04909,BMG_DS010192,Hyperprolinemia
+BMGC_DS04910,BMG_DS010193,Proline dehydrogenase deficiency
+BMGC_DS04911,BMG_DS010194,Hydroxyprolinemia
+BMGC_DS04912,BMG_DS010195,Deficiency of prolidase
+BMGC_DS04913,BMG_DS010199,Glucoglycinuria
+BMGC_DS04914,BMG_DS010200,HHH syndrome
+BMGC_DS04915,BMG_DS010201,Ornithine carbamoyltransferase deficiency
+BMGC_DS04916,BMG_DS010202,"Hyperammonemia, type III"
+BMGC_DS04917,BMG_DS010205,Late-onset citrullinemia type I
+BMGC_DS04918,BMG_DS010206,Argininosuccinic Aciduria
+BMGC_DS04919,BMG_DS010207,Hyperargininemia
+BMGC_DS04920,BMG_DS010209,Disorder of lysine AND/OR hydroxylysine metabolism
+BMGC_DS04921,BMG_DS010210,Hyperlysinemias
+BMGC_DS04922,BMG_DS010212,"Hyperlysinemia, Periodic"
+BMGC_DS04923,BMG_DS010213,Saccharopinuria
+BMGC_DS04924,BMG_DS010217,"Hyperglycinemia, Nonketotic, Type I"
+BMGC_DS04925,BMG_DS010218,"Hyperglycinemia, Nonketotic, Type II"
+BMGC_DS04926,BMG_DS010219,Sarcosinemia
+BMGC_DS04927,BMG_DS010223,Classic Maple Syrup Urine Disease
+BMGC_DS04928,BMG_DS010224,Intermittent Maple Syrup Urine Disease
+BMGC_DS04929,BMG_DS010227,Valinemia
+BMGC_DS04930,BMG_DS010228,Hyperleucine-Isoleucinemia
+BMGC_DS04931,BMG_DS010229,Isovaleryl-CoA dehydrogenase deficiency
+BMGC_DS04932,BMG_DS010232,Propionic acidemia
+BMGC_DS04933,BMG_DS010233,Holocarboxylase Synthetase Deficiency
+BMGC_DS04934,BMG_DS010234,Methylmalonic acidemia
+BMGC_DS04935,BMG_DS010238,"Glutaric aciduria, type 1"
+BMGC_DS04936,BMG_DS010239,Multiple Acyl Coenzyme A Dehydrogenase Deficiency
+BMGC_DS04937,BMG_DS010243,3-methylcrotonyl CoA carboxylase 1 deficiency
+BMGC_DS04938,BMG_DS010244,3-hydroxy-3-methylglutaric aciduria
+BMGC_DS04939,BMG_DS010245,Acetyl-CoA: carboxylase deficiency
+BMGC_DS04940,BMG_DS010248,Glutamate formiminotransferase deficiency
+BMGC_DS04941,BMG_DS010251,Disorder of sulfur-bearing amino acid metabolism
+BMGC_DS04942,BMG_DS010253,Gamma-cystathionase deficiency
+BMGC_DS04943,BMG_DS010254,Homocystinemia
+BMGC_DS04944,BMG_DS010257,Hepatic methionine adenosyltransferase deficiency
+BMGC_DS04945,BMG_DS010258,Methionine Malabsorption Syndrome
+BMGC_DS04946,BMG_DS010259,"Tyrosinemia, Type III"
+BMGC_DS04947,BMG_DS010260,Sulfite oxidase deficiency
+BMGC_DS04948,BMG_DS010261,Juvenile nephropathic cystinosis (disorder)
+BMGC_DS04949,BMG_DS010263,Hyper-beta-alaninemia
+BMGC_DS04950,BMG_DS010264,succinic semialdehyde dehydrogenase deficiency
+BMGC_DS04951,BMG_DS010265,Homocarnosinosis
+BMGC_DS04952,BMG_DS010266,Disorder of fatty acid metabolism
+BMGC_DS04953,BMG_DS010272,Histidinuria renal tubular defect
+BMGC_DS04954,BMG_DS010277,Lysinuric Protein Intolerance
+BMGC_DS04955,BMG_DS010282,Iminoglycinuria
+BMGC_DS04956,BMG_DS010294,Wet beriberi
+BMGC_DS04957,BMG_DS010295,Dry beriberi
+BMGC_DS04958,BMG_DS010302,Biotin deficiency
+BMGC_DS04959,BMG_DS010307,"Vitamin D-dependent rickets, type 1"
+BMGC_DS04960,BMG_DS010316,Uremic neuropathy
+BMGC_DS04961,BMG_DS010328,Calculous pyelonephritis
+BMGC_DS04962,BMG_DS010333,Renal glomerular disease
+BMGC_DS04963,BMG_DS010336,Acute nephropathy
+BMGC_DS04964,BMG_DS010342,"Membranoproliferative Glomerulonephritis, Type I"
+BMGC_DS04965,BMG_DS010343,"Membranoproliferative Glomerulonephritis, Type II"
+BMGC_DS04966,BMG_DS010347,Diffuse mesangial sclerosis (disorder)
+BMGC_DS04967,BMG_DS010382,Renal vascular disorder
+BMGC_DS04968,BMG_DS010391,Acquired renal cystic disease
+BMGC_DS04969,BMG_DS010402,Dipsogenic Diabetes Insipidus
+BMGC_DS04970,BMG_DS010408,Lower urinary tract infectious disease
+BMGC_DS04971,BMG_DS010421,Cystitis glandularis
+BMGC_DS04972,BMG_DS010424,Overactive Detrusor
+BMGC_DS04973,BMG_DS010531,Fibrosis of corpus cavernosum
+BMGC_DS04974,BMG_DS010545,Female acute pelvic peritonitis
+BMGC_DS04975,BMG_DS010551,Acute salpingitis
+BMGC_DS04976,BMG_DS010553,Chronic salpingitis
+BMGC_DS04977,BMG_DS010555,Salpingitis isthmica nodosa
+BMGC_DS04978,BMG_DS010557,Inflammatory disease of the uterus
+BMGC_DS04979,BMG_DS010560,Endomyometritis
+BMGC_DS04980,BMG_DS010569,Acute cervicitis
+BMGC_DS04981,BMG_DS010570,Chronic cervicitis
+BMGC_DS04982,BMG_DS010605,Endosalpingiosis
+BMGC_DS04983,BMG_DS010606,Endometriosis of cervix
+BMGC_DS04984,BMG_DS010647,uterine cervix leukoplakia
+BMGC_DS04985,BMG_DS010694,nipples inverted
+BMGC_DS04986,BMG_DS010821,mild pre-eclampsia
+BMGC_DS04987,BMG_DS010832,Pruritic urticarial papules plaques of pregnancy
+BMGC_DS04988,BMG_DS010900,Puerperal endometritis
+BMGC_DS04989,BMG_DS010954,pulmonary immaturity
+BMGC_DS04990,BMG_DS010968,Kernicterus due to isoimmunization
+BMGC_DS04991,BMG_DS010972,Lucey-Driscoll syndrome (disorder)
+BMGC_DS04992,BMG_DS010980,"Tetany, Neonatal"
+BMGC_DS04993,BMG_DS011013,nocturnal enuresis
+BMGC_DS04994,BMG_DS011014,paranoid schizophrenia
+BMGC_DS04995,BMG_DS011016,generalized anxiety disorder
+BMGC_DS04996,BMG_DS011019,Leukoencephalopathy
+BMGC_DS04997,BMG_DS011027,"Myelitis, Acute Transverse"
+BMGC_DS04998,BMG_DS011029,Epidural Abscess
+BMGC_DS04999,BMG_DS011034,Cavernous Sinus Thrombophlebitis
+BMGC_DS05000,BMG_DS011035,Lateral Sinus Thrombosis
+BMGC_DS05001,BMG_DS011087,Kluver-Bucy syndrome
+BMGC_DS05002,BMG_DS011093,"Degenerative Diseases, Central Nervous System"
+BMGC_DS05003,BMG_DS011097,Hydrocephalus Ex-Vacuo
+BMGC_DS05004,BMG_DS011101,Infantile Neuroaxonal Dystrophy
+BMGC_DS05005,BMG_DS011103,Alexander Disease
+BMGC_DS05006,BMG_DS011105,Striatonigral Degeneration
+BMGC_DS05007,BMG_DS011108,Essential Tremor
+BMGC_DS05008,BMG_DS011119,Marie Cerebellar Ataxia
+BMGC_DS05009,BMG_DS011124,Corticostriatal-Spinal Degeneration
+BMGC_DS05010,BMG_DS011132,Familial Motor Neuron Disease
+BMGC_DS05011,BMG_DS011133,"Motor Neuron Disease, Lower"
+BMGC_DS05012,BMG_DS011134,Myelopathic Muscular Atrophy
+BMGC_DS05013,BMG_DS011148,Binswanger Disease
+BMGC_DS05014,BMG_DS011165,Monoplegic Cerebral Palsy
+BMGC_DS05015,BMG_DS011168,Peroneal Nerve Paralysis
+BMGC_DS05016,BMG_DS011173,"Reflex Epilepsy, Cursive (Running)"
+BMGC_DS05017,BMG_DS011174,Gelastic Epilepsy
+BMGC_DS05018,BMG_DS011177,visual epilepsy
+BMGC_DS05019,BMG_DS011182,Focal onset impaired awareness epileptic seizure
+BMGC_DS05020,BMG_DS011183,"Secondarily generalized seizures, NOS"
+BMGC_DS05021,BMG_DS011184,Tonic Seizures
+BMGC_DS05022,BMG_DS011185,Atonic seizure
+BMGC_DS05023,BMG_DS011186,"Benign Focal Epilepsy, Childhood"
+BMGC_DS05024,BMG_DS011187,Extratemporal epilepsy
+BMGC_DS05025,BMG_DS011188,Idiopathic generalized epilepsy
+BMGC_DS05026,BMG_DS011189,benign neonatal seizures
+BMGC_DS05027,BMG_DS011190,Juvenile Myoclonic Epilepsy
+BMGC_DS05028,BMG_DS011191,Symptomatic Generalized Epilepsy
+BMGC_DS05029,BMG_DS011192,Early myoclonic encephalopathy
+BMGC_DS05030,BMG_DS011193,"Epilepsy, Reflex"
+BMGC_DS05031,BMG_DS011194,Abdominal Migraine
+BMGC_DS05032,BMG_DS011196,Basilar-Type Migraine
+BMGC_DS05033,BMG_DS011198,Hemiplegic migraine
+BMGC_DS05034,BMG_DS011204,Facial Myokymia
+BMGC_DS05035,BMG_DS011208,Facial Nerve Motor Disorders
+BMGC_DS05036,BMG_DS011209,Facial Nerve Sensory Disorders
+BMGC_DS05037,BMG_DS011230,Common peroneal nerve lesion (disorder)
+BMGC_DS05038,BMG_DS011232,Charcot-Marie-Tooth disease type 1A
+BMGC_DS05039,BMG_DS011233,Charcot-Marie-Tooth disease type 1B
+BMGC_DS05040,BMG_DS011234,"Charcot-Marie-Tooth disease, Type 1C"
+BMGC_DS05041,BMG_DS011235,Hereditary Motor and Sensory-Neuropathy Type II
+BMGC_DS05042,BMG_DS011237,Axonal neuropathy
+BMGC_DS05043,BMG_DS011238,Peripheral demyelinating neuropathy
+BMGC_DS05044,BMG_DS011244,Paraneoplastic Polyneuropathy
+BMGC_DS05045,BMG_DS011259,"Muscular Dystrophy, Oculopharyngeal"
+BMGC_DS05046,BMG_DS011264,Myotonia Levior
+BMGC_DS05047,BMG_DS011265,Congenital myopathy (disorder)
+BMGC_DS05048,BMG_DS011267,Multi-core congenital myopathy
+BMGC_DS05049,BMG_DS011272,Limb-girdle muscular dystrophy type 2H
+BMGC_DS05050,BMG_DS011273,Zebra body myopathy
+BMGC_DS05051,BMG_DS011274,Reducing-body myopathy
+BMGC_DS05052,BMG_DS011276,Cornelia De Lange Syndrome
+BMGC_DS05053,BMG_DS011293,Siderosis of eye
+BMGC_DS05054,BMG_DS011315,Macular retinal edema
+BMGC_DS05055,BMG_DS011330,Eales disease
+BMGC_DS05056,BMG_DS011335,Partial occlusion of retinal vein
+BMGC_DS05057,BMG_DS011337,dry age related macular degeneration
+BMGC_DS05058,BMG_DS011338,Exudative age-related macular degeneration
+BMGC_DS05059,BMG_DS011340,Toxic maculopathy
+BMGC_DS05060,BMG_DS011344,"Retinoschisis, Juvenile, X-Linked"
+BMGC_DS05061,BMG_DS011345,Progressive cone dystrophy (without rod involvement)
+BMGC_DS05062,BMG_DS011346,Stargardt's disease
+BMGC_DS05063,BMG_DS011348,Usher Syndrome
+BMGC_DS05064,BMG_DS011349,Disorder of ciliary body
+BMGC_DS05065,BMG_DS011368,"pupillary membrane, persistence of"
+BMGC_DS05066,BMG_DS011369,Occluded Pupils
+BMGC_DS05067,BMG_DS011377,Secondary Open Angle Glaucoma
+BMGC_DS05068,BMG_DS011378,Secondary angle-closure glaucoma
+BMGC_DS05069,BMG_DS011381,Malignant glaucoma
+BMGC_DS05070,BMG_DS011383,Aphakic glaucoma
+BMGC_DS05071,BMG_DS011389,Incipient cataract
+BMGC_DS05072,BMG_DS011391,nuclear senile cataract
+BMGC_DS05073,BMG_DS011397,Irvine-Gass Syndrome
+BMGC_DS05074,BMG_DS011399,Severe myopia
+BMGC_DS05075,BMG_DS011403,"Diplopia, Unilateral"
+BMGC_DS05076,BMG_DS011412,"Blindness, Legal"
+BMGC_DS05077,BMG_DS011428,Oculovestibuloauditory syndrome
+BMGC_DS05078,BMG_DS011433,Krukenberg spindle
+BMGC_DS05079,BMG_DS011440,Schnyder crystalline corneal dystrophy
+BMGC_DS05080,BMG_DS011459,orbit lymphoma
+BMGC_DS05081,BMG_DS011462,Glaucomatous atrophy of optic disc
+BMGC_DS05082,BMG_DS011471,Third cranial nerve disorder
+BMGC_DS05083,BMG_DS011472,Abducens Nerve Diseases
+BMGC_DS05084,BMG_DS011484,Partial Third-Nerve Palsy
+BMGC_DS05085,BMG_DS011485,Total Third-Nerve Palsy
+BMGC_DS05086,BMG_DS011486,Claude Syndrome
+BMGC_DS05087,BMG_DS011488,Fourth cranial nerve paresis
+BMGC_DS05088,BMG_DS011491,Convergence Insufficiency
+BMGC_DS05089,BMG_DS011492,Convergence Excess
+BMGC_DS05090,BMG_DS011493,Periodic Alternating Nystagmus
+BMGC_DS05091,BMG_DS011494,Symptomatic Nystagmus
+BMGC_DS05092,BMG_DS011495,Spontaneous Ocular Nystagmus
+BMGC_DS05093,BMG_DS011496,Horizontal Nystagmus
+BMGC_DS05094,BMG_DS011497,Vertical Nystagmus
+BMGC_DS05095,BMG_DS011498,Rebound Nystagmus
+BMGC_DS05096,BMG_DS011499,Pendular Nystagmus
+BMGC_DS05097,BMG_DS011500,Jerk Nystagmus
+BMGC_DS05098,BMG_DS011505,Paroxysmal Ocular Dyskinesia
+BMGC_DS05099,BMG_DS011521,Disorder of middle ear
+BMGC_DS05100,BMG_DS011522,Acute otitis media
+BMGC_DS05101,BMG_DS011525,Acute transudative otitis media
+BMGC_DS05102,BMG_DS011538,Non-suppurative otitis media
+BMGC_DS05103,BMG_DS011544,Chronic purulent otitis media
+BMGC_DS05104,BMG_DS011551,polyp of middle ear
+BMGC_DS05105,BMG_DS011611,Necrosis of pituitary
+BMGC_DS05106,BMG_DS011614,Somatotropin deficiency
+BMGC_DS05107,BMG_DS011618,"Isolated Growth Hormone Deficiency, Type II"
+BMGC_DS05108,BMG_DS011619,Laron Syndrome
+BMGC_DS05109,BMG_DS011624,"Empty Sella Syndrome, Primary"
+BMGC_DS05110,BMG_DS011625,Pituitary Dwarfism with Large Sella Turcica
+BMGC_DS05111,BMG_DS011627,Isolated gonadotropin deficiency
+BMGC_DS05112,BMG_DS011628,Female hypogonadism syndrome
+BMGC_DS05113,BMG_DS011631,Isolated lutropin deficiency (disorder)
+BMGC_DS05114,BMG_DS011632,"ACTH Deficiency, Isolated"
+BMGC_DS05115,BMG_DS011634,"prolactin deficiency, isolated"
+BMGC_DS05116,BMG_DS011655,Precocious female puberty
+BMGC_DS05117,BMG_DS011659,Hypogonadotropic hypogonadism
+BMGC_DS05118,BMG_DS011672,Type 2 diabetes mellitus in obese
+BMGC_DS05119,BMG_DS011680,Impaired glucose tolerance (disorder)
+BMGC_DS05120,BMG_DS011700,Symmetric Diabetic Proximal Motor Neuropathy
+BMGC_DS05121,BMG_DS011701,Asymmetric Diabetic Proximal Motor Neuropathy
+BMGC_DS05122,BMG_DS011703,"Polyradiculopathy, Abdominal"
+BMGC_DS05123,BMG_DS011704,Diabetic Mononeuropathy
+BMGC_DS05124,BMG_DS011706,Diabetic Polyneuropathies
+BMGC_DS05125,BMG_DS011709,"Polyneuropathy, Motor"
+BMGC_DS05126,BMG_DS011711,Diabetic Amyotrophy
+BMGC_DS05127,BMG_DS011712,Diabetic Autonomic Neuropathy
+BMGC_DS05128,BMG_DS011719,Acquired generalized lipodystrophy
+BMGC_DS05129,BMG_DS011720,Familial partial lipodystrophy
+BMGC_DS05130,BMG_DS011721,Rabson-Mendenhall Syndrome
+BMGC_DS05131,BMG_DS011731,Fasting Hypoglycemia
+BMGC_DS05132,BMG_DS011737,"Hypoglycemia, leucine-induced"
+BMGC_DS05133,BMG_DS011759,Glucocorticoid deficiency with achalasia
+BMGC_DS05134,BMG_DS011773,Lingual Goiter
+BMGC_DS05135,BMG_DS011793,isolated thyroid-stimulating hormone deficiency
+BMGC_DS05136,BMG_DS011804,Central hypothyroidism
+BMGC_DS05137,BMG_DS011827,Pendred's syndrome
+BMGC_DS05138,BMG_DS011831,X-linked reduction of thyroxine-binding globulin
+BMGC_DS05139,BMG_DS011841,Familial hyperparathyroidism
+BMGC_DS05140,BMG_DS011842,Hyperparathyroidism due to renal insufficiency
+BMGC_DS05141,BMG_DS011847,Hypercalcemia due to hyperthyroidism
+BMGC_DS05142,BMG_DS011873,Hypothalamic Pseudopuberty
+BMGC_DS05143,BMG_DS011885,Microcytic normochromic anemia
+BMGC_DS05144,BMG_DS011892,Aplastic anemia due to drugs
+BMGC_DS05145,BMG_DS011914,Anemia of chronic renal failure
+BMGC_DS05146,BMG_DS011915,"Congenital dyserythropoietic anemia, type I"
+BMGC_DS05147,BMG_DS011916,"Congenital dyserythropoietic anemia, type III"
+BMGC_DS05148,BMG_DS011950,Thiamine-responsive megaloblastic anemia
+BMGC_DS05149,BMG_DS011955,Thalassemia Intermedia
+BMGC_DS05150,BMG_DS011956,Beta zero thalassemia
+BMGC_DS05151,BMG_DS011961,Delta-Beta Thalassemia
+BMGC_DS05152,BMG_DS011966,delta-Thalassemia
+BMGC_DS05153,BMG_DS011967,Delta zero thalassemia
+BMGC_DS05154,BMG_DS011970,Hereditary persistence of fetal hemoglobin thalassemia
+BMGC_DS05155,BMG_DS011981,Hemoglobin Bart's hydrops syndrome
+BMGC_DS05156,BMG_DS012021,Xerocytosis
+BMGC_DS05157,BMG_DS012022,Rh Deficiency Syndrome
+BMGC_DS05158,BMG_DS012023,Anemia due to enzyme deficiency
+BMGC_DS05159,BMG_DS012025,G-6-PD class I variant anemia
+BMGC_DS05160,BMG_DS012033,HNSHA due to glucose phosphate isomerase deficiency
+BMGC_DS05161,BMG_DS012035,Glycogen Storage Disease XII
+BMGC_DS05162,BMG_DS012038,HNSHA due to diphosphoglycerate mutase deficiency
+BMGC_DS05163,BMG_DS012048,Hemoglobin D disease
+BMGC_DS05164,BMG_DS012052,sickle cell-hemoglobin d disease syndrome
+BMGC_DS05165,BMG_DS012054,Congenital Methemoglobinemia
+BMGC_DS05166,BMG_DS012092,Evans syndrome
+BMGC_DS05167,BMG_DS012103,Tn Syndrome
+BMGC_DS05168,BMG_DS012110,Erythrocytosis due to tissue hypoxemia
+BMGC_DS05169,BMG_DS012118,Neonatal polycythemia
+BMGC_DS05170,BMG_DS012129,Reticular dysgenesis
+BMGC_DS05171,BMG_DS012132,Shwachman syndrome
+BMGC_DS05172,BMG_DS012136,Lazy Leukocyte Syndrome
+BMGC_DS05173,BMG_DS012138,Alloimmune neonatal neutropenia
+BMGC_DS05174,BMG_DS012140,Drug-induced neutropenia
+BMGC_DS05175,BMG_DS012147,Congenital leukocyte adherence deficiency
+BMGC_DS05176,BMG_DS012151,Familial eosinophilia
+BMGC_DS05177,BMG_DS012158,Familial Hemophagocytic Lymphocytosis
+BMGC_DS05178,BMG_DS012160,extracutaneous mastocytoma
+BMGC_DS05179,BMG_DS012161,indolent systemic mastocytosis
+BMGC_DS05180,BMG_DS012184,SCID (severe combined immunodeficiency) due to absent adenosine deaminase
+BMGC_DS05181,BMG_DS012189,Hyperimmunoglobulin M syndrome
+BMGC_DS05182,BMG_DS012190,Transient hypogammaglobulinemia of infancy
+BMGC_DS05183,BMG_DS012193,Complement Deficiencies
+BMGC_DS05184,BMG_DS012204,solitary osseous plasmacytoma
+BMGC_DS05185,BMG_DS012231,Heparin-induced thrombocytopenia
+BMGC_DS05186,BMG_DS012232,Thrombocytopenia due to platelet alloimmunization
+BMGC_DS05187,BMG_DS012237,Chronic idiopathic thrombocytopenic purpura
+BMGC_DS05188,BMG_DS012245,Gray Platelet Syndrome
+BMGC_DS05189,BMG_DS012256,Coagulation factor deficiency syndrome
+BMGC_DS05190,BMG_DS012258,Hereditary factor II deficiency disease
+BMGC_DS05191,BMG_DS012261,Hereditary factor VII deficiency disease
+BMGC_DS05192,BMG_DS012263,Severe hereditary factor VIII deficiency disease
+BMGC_DS05193,BMG_DS012264,Moderate hereditary factor VIII deficiency disease
+BMGC_DS05194,BMG_DS012265,Mild hereditary factor VIII deficiency disease
+BMGC_DS05195,BMG_DS012266,"Factor 8 deficiency, acquired"
+BMGC_DS05196,BMG_DS012267,Hereditary factor X deficiency disease
+BMGC_DS05197,BMG_DS012276,Prekallikrein deficiency
+BMGC_DS05198,BMG_DS012277,High molecular weight kininogen deficiency
+BMGC_DS05199,BMG_DS012286,"Dysfibrinogenemia, Congenital"
+BMGC_DS05200,BMG_DS012294,Acquired von Willebrand disease
+BMGC_DS05201,BMG_DS012303,Drug-induced coagulation inhibitor disorder
+BMGC_DS05202,BMG_DS012305,Antithrombin III Deficiency
+BMGC_DS05203,BMG_DS012318,Disorder of lymph node
+BMGC_DS05204,BMG_DS012329,Nontraumatic splenic rupture
+BMGC_DS05205,BMG_DS012332,Splenic abscess
+BMGC_DS05206,BMG_DS012428,Acute infectious disease
+BMGC_DS05207,BMG_DS012449,Acute bacterial peritonitis
+BMGC_DS05208,BMG_DS012454,Acute bacterial epiglottitis
+BMGC_DS05209,BMG_DS012455,Acute bacterial sinusitis
+BMGC_DS05210,BMG_DS012458,Pulmonary actinomycosis
+BMGC_DS05211,BMG_DS012468,Nocardia asteroides Infection
+BMGC_DS05212,BMG_DS012471,Pulmonary Nocardiosis
+BMGC_DS05213,BMG_DS012522,Acute gonococcal urethritis
+BMGC_DS05214,BMG_DS012524,Acute gonococcal salpingitis
+BMGC_DS05215,BMG_DS012532,Gonorrhea of rectum
+BMGC_DS05216,BMG_DS012598,Infection due to Bordetella parapertussis (disorder)
+BMGC_DS05217,BMG_DS012611,Pneumococcal pharyngitis
+BMGC_DS05218,BMG_DS012627,Lyme carditis
+BMGC_DS05219,BMG_DS012637,Staphylococcal tonsillitis
+BMGC_DS05220,BMG_DS012638,Staphylococcal pharyngitis
+BMGC_DS05221,BMG_DS012647,Streptococcal tonsillitis
+BMGC_DS05222,BMG_DS012682,"Early latent syphilis, positive serology, negative cerebrospinal fluid, less than 2 years after infection"
+BMGC_DS05223,BMG_DS012784,Acute tuberculosis
+BMGC_DS05224,BMG_DS012800,Infection by Campylobacter fetus
+BMGC_DS05225,BMG_DS012803,Enteric campylobacteriosis
+BMGC_DS05226,BMG_DS012809,Initial lesion of yaws
+BMGC_DS05227,BMG_DS012813,Early yaws
+BMGC_DS05228,BMG_DS012819,Yaws gummata and ulcers
+BMGC_DS05229,BMG_DS012836,Haemophilus influenzae pneumonia
+BMGC_DS05230,BMG_DS012837,Haemophilus influenzae otitis media
+BMGC_DS05231,BMG_DS012867,Sepsis caused by Bacteroides
+BMGC_DS05232,BMG_DS012873,Infection caused by Pseudomonas aeruginosa
+BMGC_DS05233,BMG_DS012875,Malignant otitis media
+BMGC_DS05234,BMG_DS012881,Ecthyma gangrenosum
+BMGC_DS05235,BMG_DS012883,Escherichia coli septicemia
+BMGC_DS05236,BMG_DS012884,Pneumonia caused by Escherichia coli
+BMGC_DS05237,BMG_DS012923,Viral myocarditis
+BMGC_DS05238,BMG_DS012960,Monkeypox (disorder)
+BMGC_DS05239,BMG_DS012997,Recurrent herpes simplex
+BMGC_DS05240,BMG_DS013000,Herpes encephalitis
+BMGC_DS05241,BMG_DS013002,Herpes simplex keratoconjunctivitis
+BMGC_DS05242,BMG_DS013030,Verruca plana
+BMGC_DS05243,BMG_DS013052,Zika Virus Infection
+BMGC_DS05244,BMG_DS013106,"Influenza due to Influenza virus, type B"
+BMGC_DS05245,BMG_DS013213,familial Alzheimer disease
+BMGC_DS05246,BMG_DS013215,Human immunodeficiency virus I infection
+BMGC_DS05247,BMG_DS013266,Nutritional deficiency with AIDS (acquired immunodeficiency syndrome)
+BMGC_DS05248,BMG_DS013285,Chronic viral hepatitis B without delta-agent
+BMGC_DS05249,BMG_DS013317,Mycotic endocarditis
+BMGC_DS05250,BMG_DS013322,Invasive Pulmonary Aspergillosis
+BMGC_DS05251,BMG_DS013333,Disseminated coccidioidomycosis
+BMGC_DS05252,BMG_DS013345,Neonatal candidiasis
+BMGC_DS05253,BMG_DS013349,Pulmonary cryptococcosis
+BMGC_DS05254,BMG_DS013384,Disseminated sporotrichosis
+BMGC_DS05255,BMG_DS013386,Lymphocutaneous sporotrichosis
+BMGC_DS05256,BMG_DS013401,Kerion celsi
+BMGC_DS05257,BMG_DS013413,Onychomycosis caused by Trichophyton rubrum
+BMGC_DS05258,BMG_DS013414,Onychomycosis caused by Trichophyton mentagrophytes
+BMGC_DS05259,BMG_DS013417,Fusariosis
+BMGC_DS05260,BMG_DS013471,Meningoencephalitis caused by Naegleria
+BMGC_DS05261,BMG_DS013556,Schistosoma hematobium infection
+BMGC_DS05262,BMG_DS013562,Infection by Schistosoma intercalatum
+BMGC_DS05263,BMG_DS013625,Opisthorchis felineus Infection
+BMGC_DS05264,BMG_DS013626,Opisthorchis viverrini Infection
+BMGC_DS05265,BMG_DS013736,Angiostrongylus cantonensis infection
+BMGC_DS05266,BMG_DS013753,Infection by Baylisascaris
+BMGC_DS05267,BMG_DS013922,Infection by Moniliformis
+BMGC_DS05268,BMG_DS013942,Flea Infestation
+BMGC_DS05269,BMG_DS014094,Infectious colitis
+BMGC_DS05270,BMG_DS014095,Infectious gastroenteritis
+BMGC_DS05271,BMG_DS014098,Traveler's diarrhea
+BMGC_DS05272,BMG_DS014143,"Hemiplegia, Crossed"
+BMGC_DS05273,BMG_DS014153,facial spasm
+BMGC_DS05274,BMG_DS014164,"Reflex Epilepsy, Reading"
+BMGC_DS05275,BMG_DS014168,"Reflex Epilepsy, Musicogenic"
+BMGC_DS05276,BMG_DS014176,childhood medulloblastoma
+BMGC_DS05277,BMG_DS014177,localized osteosarcoma
+BMGC_DS05278,BMG_DS014178,childhood cerebellar astrocytic neoplasm
+BMGC_DS05279,BMG_DS014179,adult fibrosarcoma
+BMGC_DS05280,BMG_DS014180,pediatric infratentorial ependymoma
+BMGC_DS05281,BMG_DS014181,childhood brain stem glioma
+BMGC_DS05282,BMG_DS014182,inflammatory breast carcinoma
+BMGC_DS05283,BMG_DS014183,adult liposarcoma
+BMGC_DS05284,BMG_DS014184,extramedullary plasmacytoma
+BMGC_DS05285,BMG_DS014185,refractory plasma cell neoplasm
+BMGC_DS05286,BMG_DS014186,adult malignant schwannoma
+BMGC_DS05287,BMG_DS014187,pediatric supratentorial ependymoma
+BMGC_DS05288,BMG_DS014188,childhood optic nerve glioma
+BMGC_DS05289,BMG_DS014189,gastric adenocarcinoma
+BMGC_DS05290,BMG_DS014191,intraocular retinoblastoma
+BMGC_DS05291,BMG_DS014192,extraocular retinoblastoma
+BMGC_DS05292,BMG_DS014193,malignant mesothelioma
+BMGC_DS05293,BMG_DS014194,childhood central nervous system germ cell tumor
+BMGC_DS05294,BMG_DS014195,gestational trophoblastic neoplasm
+BMGC_DS05295,BMG_DS014196,small intestine adenocarcinoma
+BMGC_DS05296,BMG_DS014197,duodenal adenocarcinoma
+BMGC_DS05297,BMG_DS014198,small intestine lymphoma
+BMGC_DS05298,BMG_DS014199,gallbladder cancer
+BMGC_DS05299,BMG_DS014200,invasive malignant thymoma
+BMGC_DS05300,BMG_DS014201,noninvasive malignant thymoma
+BMGC_DS05301,BMG_DS014204,growth hormone-producing pituitary gland adenoma
+BMGC_DS05302,BMG_DS014205,small size posterior uveal melanoma
+BMGC_DS05303,BMG_DS014206,medium/large size posterior uveal melanoma
+BMGC_DS05304,BMG_DS014208,adult brainstem glioma
+BMGC_DS05305,BMG_DS014209,adult medulloblastoma
+BMGC_DS05306,BMG_DS014210,adult glioblastoma
+BMGC_DS05307,BMG_DS014211,metastatic melanoma
+BMGC_DS05308,BMG_DS014212,adult extraskeletal osteosarcoma
+BMGC_DS05309,BMG_DS014213,head and neck cancer
+BMGC_DS05310,BMG_DS014214,carcinoma of liver and intrahepatic biliary tract
+BMGC_DS05311,BMG_DS014215,childhood germ cell tumor
+BMGC_DS05312,BMG_DS014216,grade I lymphomatoid granulomatosis
+BMGC_DS05313,BMG_DS014218,adult oligodendroglioma
+BMGC_DS05314,BMG_DS014220,ovarian seromucinous carcinoma
+BMGC_DS05315,BMG_DS014222,"chronic myelogenous leukemia, BCR-ABL1 positive"
+BMGC_DS05316,BMG_DS014223,alveolar soft part sarcoma
+BMGC_DS05317,BMG_DS014224,adult epithelioid sarcoma
+BMGC_DS05318,BMG_DS014225,adult malignant hemangiopericytoma
+BMGC_DS05319,BMG_DS014226,adult malignant mesenchymoma
+BMGC_DS05320,BMG_DS014227,adenosquamous lung carcinoma
+BMGC_DS05321,BMG_DS014229,invasive lobular breast carcinoma
+BMGC_DS05322,BMG_DS014232,T-cell adult acute lymphocytic leukemia
+BMGC_DS05323,BMG_DS014234,fibrosarcomatous osteosarcoma
+BMGC_DS05324,BMG_DS014235,chondroblastic osteosarcoma
+BMGC_DS05325,BMG_DS014236,pediatric hepatocellular carcinoma
+BMGC_DS05326,BMG_DS014237,adult hepatocellular carcinoma
+BMGC_DS05327,BMG_DS014238,epithelial predominant Wilms' tumor
+BMGC_DS05328,BMG_DS014239,blastema predominant kidney Wilms tumor
+BMGC_DS05329,BMG_DS014240,stromal predominant kidney Wilms tumor
+BMGC_DS05330,BMG_DS014241,mixed cell type kidney Wilms' tumor
+BMGC_DS05331,BMG_DS014242,alveolar rhabdomyosarcoma
+BMGC_DS05332,BMG_DS014243,childhood pleomorphic rhabdomyosarcoma
+BMGC_DS05333,BMG_DS014244,small cell osteogenic sarcoma
+BMGC_DS05334,BMG_DS014245,esophageal squamous cell carcinoma
+BMGC_DS05335,BMG_DS014246,esophageal adenocarcinoma
+BMGC_DS05336,BMG_DS014248,diffuse gastric adenocarcinoma
+BMGC_DS05337,BMG_DS014249,anal carcinoma
+BMGC_DS05338,BMG_DS014250,colon mucinous adenocarcinoma
+BMGC_DS05339,BMG_DS014252,gallbladder adenocarcinoma
+BMGC_DS05340,BMG_DS014253,rectum mucinous adenocarcinoma
+BMGC_DS05341,BMG_DS014255,rectal signet ring cell adenocarcinoma
+BMGC_DS05342,BMG_DS014256,gallbladder squamous cell carcinoma
+BMGC_DS05343,BMG_DS014257,extrahepatic bile duct adenocarcinoma
+BMGC_DS05344,BMG_DS014258,pancreatic acinar cell carcinoma
+BMGC_DS05345,BMG_DS014259,ovarian serous cystadenocarcinoma
+BMGC_DS05346,BMG_DS014260,ovarian mucinous cystadenocarcinoma
+BMGC_DS05347,BMG_DS014261,ovarian clear cell cystadenocarcinoma
+BMGC_DS05348,BMG_DS014263,cervical squamous cell carcinoma
+BMGC_DS05349,BMG_DS014264,cervical adenocarcinoma
+BMGC_DS05350,BMG_DS014265,cervical small cell carcinoma
+BMGC_DS05351,BMG_DS014266,bladder transitional cell carcinoma
+BMGC_DS05352,BMG_DS014267,bladder squamous cell carcinoma
+BMGC_DS05353,BMG_DS014268,bladder adenocarcinoma
+BMGC_DS05354,BMG_DS014270,intermediate cell type uveal melanoma
+BMGC_DS05355,BMG_DS014271,necrotic uveal melanoma
+BMGC_DS05356,BMG_DS014272,salivary gland squamous cell carcinoma
+BMGC_DS05357,BMG_DS014274,parathyroid gland clear cell adenoma
+BMGC_DS05358,BMG_DS014275,mixed cell type adenoma of parathyroid
+BMGC_DS05359,BMG_DS014276,clear cell renal carcinoma
+BMGC_DS05360,BMG_DS014277,thymoma type B3
+BMGC_DS05361,BMG_DS014278,lymphoepithelioma-like thymic carcinoma
+BMGC_DS05362,BMG_DS014279,malignant type A thymoma
+BMGC_DS05363,BMG_DS014280,testicular yolk sac tumor
+BMGC_DS05364,BMG_DS014284,endometrial adenocarcinoma
+BMGC_DS05365,BMG_DS014285,endometrial clear cell adenocarcinoma
+BMGC_DS05366,BMG_DS014286,refractory hairy cell leukemia
+BMGC_DS05367,BMG_DS014287,anterior urethra cancer
+BMGC_DS05368,BMG_DS014288,posterior urethra cancer
+BMGC_DS05369,BMG_DS014289,extraskeletal Ewing sarcoma
+BMGC_DS05370,BMG_DS014290,pediatric fibrosarcoma
+BMGC_DS05371,BMG_DS014291,childhood malignant hemangiopericytoma
+BMGC_DS05372,BMG_DS014292,pediatric liposarcoma
+BMGC_DS05373,BMG_DS014293,alveolar soft part sarcoma
+BMGC_DS05374,BMG_DS014294,childhood malignant schwannoma
+BMGC_DS05375,BMG_DS014295,pediatric angiosarcoma
+BMGC_DS05376,BMG_DS014296,childhood epithelioid sarcoma
+BMGC_DS05377,BMG_DS014297,childhood malignant mesenchymoma
+BMGC_DS05378,BMG_DS014299,lung carcinoid tumor
+BMGC_DS05379,BMG_DS014300,ovarian teratoma
+BMGC_DS05380,BMG_DS014301,ovarian monodermal and highly specialized teratoma
+BMGC_DS05381,BMG_DS014302,ovarian mixed germ cell neoplasm
+BMGC_DS05382,BMG_DS014303,acute undifferentiated leukemia
+BMGC_DS05383,BMG_DS014307,squamous cell carcinoma of lip
+BMGC_DS05384,BMG_DS014311,oropharynx squamous cell carcinoma
+BMGC_DS05385,BMG_DS014313,hypopharynx squamous cell carcinoma
+BMGC_DS05386,BMG_DS014314,laryngeal squamous cell carcinoma
+BMGC_DS05387,BMG_DS014315,glottis squamous cell carcinoma
+BMGC_DS05388,BMG_DS014316,subglottis squamous cell carcinoma
+BMGC_DS05389,BMG_DS014317,larynx verrucous carcinoma
+BMGC_DS05390,BMG_DS014318,glottis verrucous carcinoma
+BMGC_DS05391,BMG_DS014319,subglottis verrucous carcinoma
+BMGC_DS05392,BMG_DS014320,supraglottis verrucous carcinoma
+BMGC_DS05393,BMG_DS014321,nasal cavity and paranasal sinus squamous cell carcinoma
+BMGC_DS05394,BMG_DS014322,nasal cavity squamous cell carcinoma
+BMGC_DS05395,BMG_DS014323,paranasal sinus squamous cell carcinoma
+BMGC_DS05396,BMG_DS014324,nasal cavity inverting papilloma
+BMGC_DS05397,BMG_DS014325,anus basaloid carcinoma
+BMGC_DS05398,BMG_DS014326,childhood oligodendroglioma
+BMGC_DS05399,BMG_DS014327,childhood choroid plexus neoplasm
+BMGC_DS05400,BMG_DS014328,uterine carcinosarcoma
+BMGC_DS05401,BMG_DS014329,leiomyosarcoma of the corpus uteri
+BMGC_DS05402,BMG_DS014331,pediatric meningioma
+BMGC_DS05403,BMG_DS014332,cholangiocarcinoma
+BMGC_DS05404,BMG_DS014333,ovarian sarcoma
+BMGC_DS05405,BMG_DS014334,juvenile pilocytic astrocytoma
+BMGC_DS05406,BMG_DS014336,adult anaplastic ependymoma
+BMGC_DS05407,BMG_DS014337,anaplastic ependymoma
+BMGC_DS05408,BMG_DS014338,mixed astrocytoma-ependymoma
+BMGC_DS05409,BMG_DS014339,mixed astrocytoma-ependymoma-oligodendroglioma
+BMGC_DS05410,BMG_DS014340,mixed oligodendroglioma-astrocytoma
+BMGC_DS05411,BMG_DS014341,adult pineal parenchymal tumor
+BMGC_DS05412,BMG_DS014342,pineal gland astrocytoma
+BMGC_DS05413,BMG_DS014343,adult central nervous system germ cell tumor
+BMGC_DS05414,BMG_DS014345,primary central nervous system lymphoma
+BMGC_DS05415,BMG_DS014346,vulvar squamous cell carcinoma
+BMGC_DS05416,BMG_DS014349,bilateral breast carcinoma
+BMGC_DS05417,BMG_DS014350,adult infiltrating astrocytic neoplasm
+BMGC_DS05418,BMG_DS014351,"adult embryonal tumor with multilayered rosettes, c19mc-altered"
+BMGC_DS05419,BMG_DS014352,adult pineoblastoma
+BMGC_DS05420,BMG_DS014353,adult papillary meningioma
+BMGC_DS05421,BMG_DS014354,pancreatic adenocarcinoma
+BMGC_DS05422,BMG_DS014356,desmoplastic small round cell tumor
+BMGC_DS05423,BMG_DS014357,intraocular lymphoma
+BMGC_DS05424,BMG_DS014377,"Chondrodysplasia punctata, X-linked dominant type"
+BMGC_DS05425,BMG_DS014378,neurotic depression
+BMGC_DS05426,BMG_DS014379,aplasia cutis congenita
+BMGC_DS05427,BMG_DS014381,Iron Overload
+BMGC_DS05428,BMG_DS014383,Cronkhite-Canada Syndrome
+BMGC_DS05429,BMG_DS014384,Amaurotic Familial Idiocy
+BMGC_DS05430,BMG_DS014387,Bubonic Plague
+BMGC_DS05431,BMG_DS014388,Interstitial Cystitis
+BMGC_DS05432,BMG_DS014389,Sneddon Syndrome
+BMGC_DS05433,BMG_DS014390,Environmental Illness
+BMGC_DS05434,BMG_DS014391,Landau-Kleffner Syndrome
+BMGC_DS05435,BMG_DS014392,primary progressive aphasia
+BMGC_DS05436,BMG_DS014393,"Adrenoleukodystrophy, Neonatal"
+BMGC_DS05437,BMG_DS014394,Hyperpipecolic Acidemia
+BMGC_DS05438,BMG_DS014395,"Refsum Disease, Infantile"
+BMGC_DS05439,BMG_DS014396,Peroxisomal Disorders
+BMGC_DS05440,BMG_DS014397,"Chondrodysplasia Punctata, Rhizomelic"
+BMGC_DS05441,BMG_DS014398,Leukostasis
+BMGC_DS05442,BMG_DS014399,Persian Gulf Syndrome
+BMGC_DS05443,BMG_DS014400,Congenital Disorders of Glycosylation
+BMGC_DS05444,BMG_DS014401,myomatous neoplasm
+BMGC_DS05445,BMG_DS014402,vascular neoplasm
+BMGC_DS05446,BMG_DS014403,bone marrow neoplasm
+BMGC_DS05447,BMG_DS014406,"Smith-Lemli-Opitz Syndrome, Type I"
+BMGC_DS05448,BMG_DS014407,"Smith-Lemli-Opitz Syndrome, Type II"
+BMGC_DS05449,BMG_DS014410,"Hemorrhagic Fever, Ebola"
+BMGC_DS05450,BMG_DS014411,Phycomycosis
+BMGC_DS05451,BMG_DS014413,Alymphocytosis
+BMGC_DS05452,BMG_DS014414,caudal regression sequence
+BMGC_DS05453,BMG_DS014423,trabecular adenocarcinoma
+BMGC_DS05454,BMG_DS014426,lytic metastatic bone lesion
+BMGC_DS05455,BMG_DS014427,Xanthoma
+BMGC_DS05456,BMG_DS014428,"Porokeratosis, Linear"
+BMGC_DS05457,BMG_DS014429,meningeal sarcoma
+BMGC_DS05458,BMG_DS014433,Brucella melitensis brucellosis
+BMGC_DS05459,BMG_DS014434,Brucella abortus brucellosis
+BMGC_DS05460,BMG_DS014436,Alcohol Withdrawal Hallucinosis
+BMGC_DS05461,BMG_DS014441,cervical carcinoma
+BMGC_DS05462,BMG_DS014442,Fulminant Hepatitis
+BMGC_DS05463,BMG_DS014444,Euthyroid Goiter
+BMGC_DS05464,BMG_DS014446,porencephaly
+BMGC_DS05465,BMG_DS014452,Pustular folliculitis
+BMGC_DS05466,BMG_DS014455,Frozen shoulder
+BMGC_DS05467,BMG_DS014457,Congenital cystic kidney disease
+BMGC_DS05468,BMG_DS014458,cryptophthalmia
+BMGC_DS05469,BMG_DS014459,buphthalmos
+BMGC_DS05470,BMG_DS014460,Chronic mesenteric ischemia
+BMGC_DS05471,BMG_DS014463,Ascending cholangitis
+BMGC_DS05472,BMG_DS014465,Lipoid dermatoarthritis
+BMGC_DS05473,BMG_DS014475,Grand Mal Status Epilepticus
+BMGC_DS05474,BMG_DS014477,fundus albipunctatus
+BMGC_DS05475,BMG_DS014487,Lupus anticoagulant disorder
+BMGC_DS05476,BMG_DS014491,Isosporiasis
+BMGC_DS05477,BMG_DS014493,Nonspecific urethritis
+BMGC_DS05478,BMG_DS014494,hyperbilirubinemia
+BMGC_DS05479,BMG_DS014500,congenital contractures
+BMGC_DS05480,BMG_DS014521,mucositis
+BMGC_DS05481,BMG_DS014538,amyloid tumor
+BMGC_DS05482,BMG_DS014544,Focal Nodular Hyperplasia
+BMGC_DS05483,BMG_DS014546,clear cell acanthoma
+BMGC_DS05484,BMG_DS014553,inverted follicular keratosis
+BMGC_DS05485,BMG_DS014557,nephrogenic adenoma
+BMGC_DS05486,BMG_DS014558,Osteoma cutis
+BMGC_DS05487,BMG_DS014562,"Fibrocystic change, proliferative type with atypia"
+BMGC_DS05488,BMG_DS014564,Epidermal Nevus
+BMGC_DS05489,BMG_DS014566,Lymphangiomatosis
+BMGC_DS05490,BMG_DS014569,inflammatory myofibroblastic tumor
+BMGC_DS05491,BMG_DS014572,"Histiocytosis, Familial Lipochrome"
+BMGC_DS05492,BMG_DS014578,malignant giant cell tumor
+BMGC_DS05493,BMG_DS014581,pleomorphic carcinoma
+BMGC_DS05494,BMG_DS014582,small cell carcinoma
+BMGC_DS05495,BMG_DS014583,verrucous papilloma
+BMGC_DS05496,BMG_DS014584,papillary squamous carcinoma
+BMGC_DS05497,BMG_DS014587,keratinizing squamous cell carcinoma
+BMGC_DS05498,BMG_DS014588,adenoid squamous cell carcinoma
+BMGC_DS05499,BMG_DS014589,nasopharyngeal type undifferentiated carcinoma
+BMGC_DS05500,BMG_DS014590,superficial multifocal basal cell carcinoma
+BMGC_DS05501,BMG_DS014592,Borst-Jadassohn intraepidermal carcinoma
+BMGC_DS05502,BMG_DS014594,transitional cell neoplasm
+BMGC_DS05503,BMG_DS014595,transitional cell papilloma
+BMGC_DS05504,BMG_DS014596,inverted transitional papilloma
+BMGC_DS05505,BMG_DS014597,non-keratinizing sinonasal squamous cell carcinoma
+BMGC_DS05506,BMG_DS014598,sarcomatoid transitional cell carcinoma
+BMGC_DS05507,BMG_DS014599,cloacogenic carcinoma
+BMGC_DS05508,BMG_DS014600,papillary transitional cell carcinoma
+BMGC_DS05509,BMG_DS014601,adenocarcinoma in situ
+BMGC_DS05510,BMG_DS014603,diffuse type adenocarcinoma
+BMGC_DS05511,BMG_DS014604,bile duct cystadenoma
+BMGC_DS05512,BMG_DS014605,bile duct mucinous cystic neoplasm with an associated invasive carcinoma
+BMGC_DS05513,BMG_DS014606,fibrolamellar hepatocellular carcinoma
+BMGC_DS05514,BMG_DS014610,alveoli adenoma
+BMGC_DS05515,BMG_DS014611,villous adenocarcinoma
+BMGC_DS05516,BMG_DS014613,pituitary gland mixed eosinophil-basophil adenoma
+BMGC_DS05517,BMG_DS014614,basophilic adenocarcinoma
+BMGC_DS05518,BMG_DS014615,clear cell adenoma
+BMGC_DS05519,BMG_DS014616,clear cell adenofibroma
+BMGC_DS05520,BMG_DS014617,lipid-rich carcinoma
+BMGC_DS05521,BMG_DS014618,glycogen-rich carcinoma
+BMGC_DS05522,BMG_DS014619,chief cell adenoma
+BMGC_DS05523,BMG_DS014620,water-clear cell adenoma
+BMGC_DS05524,BMG_DS014621,clear cell adenocarcinoma
+BMGC_DS05525,BMG_DS014622,mixed cell adenoma
+BMGC_DS05526,BMG_DS014623,lipoadenoma
+BMGC_DS05527,BMG_DS014624,trabecular follicular adenocarcinoma
+BMGC_DS05528,BMG_DS014625,thyroid gland fetal adenoma
+BMGC_DS05529,BMG_DS014626,thyroid gland macrofollicular adenoma
+BMGC_DS05530,BMG_DS014627,thyroid gland diffuse sclerosing papillary carcinoma
+BMGC_DS05531,BMG_DS014629,apocrine adenoma
+BMGC_DS05532,BMG_DS014630,apocrine adenocarcinoma
+BMGC_DS05533,BMG_DS014631,benign spiradenoma
+BMGC_DS05534,BMG_DS014632,papillary hidradenoma
+BMGC_DS05535,BMG_DS014633,eccrine papillary adenoma
+BMGC_DS05536,BMG_DS014634,ceruminoma
+BMGC_DS05537,BMG_DS014635,ceruminous carcinoma
+BMGC_DS05538,BMG_DS014637,serous surface papilloma
+BMGC_DS05539,BMG_DS014638,mucin-producing carcinoma
+BMGC_DS05540,BMG_DS014640,breast secretory carcinoma
+BMGC_DS05541,BMG_DS014641,intracystic papillary adenoma
+BMGC_DS05542,BMG_DS014645,adenoma
+BMGC_DS05543,BMG_DS014646,epithelial-myoepithelial carcinoma
+BMGC_DS05544,BMG_DS014647,adenoid squamous cell carcinoma
+BMGC_DS05545,BMG_DS014648,granulosa cell tumor
+BMGC_DS05546,BMG_DS014649,juvenile type testicular granulosa cell tumor
+BMGC_DS05547,BMG_DS014652,malignant Leydig cell tumor
+BMGC_DS05548,BMG_DS014657,glomangioma
+BMGC_DS05549,BMG_DS014658,glomangiomyoma
+BMGC_DS05550,BMG_DS014659,nodular malignant melanoma
+BMGC_DS05551,BMG_DS014660,balloon cell malignant melanoma
+BMGC_DS05552,BMG_DS014662,epithelioid cell melanoma
+BMGC_DS05553,BMG_DS014663,spindle cell melanoma
+BMGC_DS05554,BMG_DS014665,sarcomatosis
+BMGC_DS05555,BMG_DS014666,congenital fibrosarcoma
+BMGC_DS05556,BMG_DS014668,undifferentiated pleomorphic sarcoma
+BMGC_DS05557,BMG_DS014670,sclerosing liposarcoma
+BMGC_DS05558,BMG_DS014671,round cell liposarcoma
+BMGC_DS05559,BMG_DS014672,mixed liposarcoma
+BMGC_DS05560,BMG_DS014673,infiltrating lipoma
+BMGC_DS05561,BMG_DS014674,spindle cell lipoma
+BMGC_DS05562,BMG_DS014675,cellular leiomyoma
+BMGC_DS05563,BMG_DS014676,bizarre leiomyoma
+BMGC_DS05564,BMG_DS014677,pleomorphic rhabdomyosarcoma
+BMGC_DS05565,BMG_DS014678,mixed type rhabdomyosarcoma
+BMGC_DS05566,BMG_DS014680,clear cell sarcoma of kidney
+BMGC_DS05567,BMG_DS014681,pancreatoblastoma
+BMGC_DS05568,BMG_DS014683,malignant mesenchymoma
+BMGC_DS05569,BMG_DS014684,malignant ovarian Brenner tumor
+BMGC_DS05570,BMG_DS014685,breast intracanalicular fibroadenoma
+BMGC_DS05571,BMG_DS014686,breast pericanalicular fibroadenoma
+BMGC_DS05572,BMG_DS014688,mucinous adenofibroma
+BMGC_DS05573,BMG_DS014690,spindle cell synovial sarcoma
+BMGC_DS05574,BMG_DS014691,epithelioid cell synovial sarcoma
+BMGC_DS05575,BMG_DS014692,biphasic synovial sarcoma
+BMGC_DS05576,BMG_DS014693,benign fibrous mesothelioma
+BMGC_DS05577,BMG_DS014694,sarcomatoid mesothelioma
+BMGC_DS05578,BMG_DS014695,malignant biphasic mesothelioma
+BMGC_DS05579,BMG_DS014696,spermatocytic seminoma
+BMGC_DS05580,BMG_DS014698,immature teratoma
+BMGC_DS05581,BMG_DS014699,intermediate malignant teratoma
+BMGC_DS05582,BMG_DS014701,mixed germ cell tumor
+BMGC_DS05583,BMG_DS014702,malignant struma ovarii
+BMGC_DS05584,BMG_DS014703,partial hydatidiform mole
+BMGC_DS05585,BMG_DS014707,arteriovenous hemangioma/malformation
+BMGC_DS05586,BMG_DS014709,verrucous hemangioma
+BMGC_DS05587,BMG_DS014710,"hemangiopericytoma, malignant"
+BMGC_DS05588,BMG_DS014712,osteosarcoma arising in bone Paget disease
+BMGC_DS05589,BMG_DS014713,periosteal chondroma
+BMGC_DS05590,BMG_DS014714,periosteal chondrosarcoma
+BMGC_DS05591,BMG_DS014715,myxoid chondrosarcoma
+BMGC_DS05592,BMG_DS014716,malignancy in giant cell tumor of bone
+BMGC_DS05593,BMG_DS014718,malignant giant cell tumor of soft parts
+BMGC_DS05594,BMG_DS014719,adamantinoma
+BMGC_DS05595,BMG_DS014722,gliomatosis cerebri
+BMGC_DS05596,BMG_DS014723,papillary ependymoma
+BMGC_DS05597,BMG_DS014724,anaplastic astrocytoma
+BMGC_DS05598,BMG_DS014725,protoplasmic astrocytoma
+BMGC_DS05599,BMG_DS014726,gemistocytic astrocytoma
+BMGC_DS05600,BMG_DS014727,fibrillary astrocytoma
+BMGC_DS05601,BMG_DS014728,pilocytic astrocytoma
+BMGC_DS05602,BMG_DS014729,pleomorphic xanthoastrocytoma
+BMGC_DS05603,BMG_DS014730,astroblastoma
+BMGC_DS05604,BMG_DS014731,giant cell glioblastoma
+BMGC_DS05605,BMG_DS014732,anaplastic oligodendroglioma
+BMGC_DS05606,BMG_DS014734,Pacinian tumor
+BMGC_DS05607,BMG_DS014735,meningothelial meningioma
+BMGC_DS05608,BMG_DS014736,fibrous meningioma
+BMGC_DS05609,BMG_DS014737,psammomatous meningioma
+BMGC_DS05610,BMG_DS014738,angiomatous meningioma
+BMGC_DS05611,BMG_DS014739,transitional meningioma
+BMGC_DS05612,BMG_DS014740,sarcomatosis of the meninges
+BMGC_DS05613,BMG_DS014741,malignant triton tumor
+BMGC_DS05614,BMG_DS014742,granular cell cancer
+BMGC_DS05615,BMG_DS014743,lymphoplasmacytic lymphoma
+BMGC_DS05616,BMG_DS014744,intravascular large B-cell lymphoma
+BMGC_DS05617,BMG_DS014745,histiocytic sarcoma
+BMGC_DS05618,BMG_DS014746,mast cell neoplasm
+BMGC_DS05619,BMG_DS014749,renal adenoma
+BMGC_DS05620,BMG_DS014750,endometrial stromal tumor
+BMGC_DS05621,BMG_DS014751,malignant myoepithelioma
+BMGC_DS05622,BMG_DS014752,childhood cerebral astrocytoma
+BMGC_DS05623,BMG_DS014753,silent pituitary adenoma
+BMGC_DS05624,BMG_DS014754,colon adenocarcinoma
+BMGC_DS05625,BMG_DS014755,uterine corpus sarcoma
+BMGC_DS05626,BMG_DS014767,"Meningitis, Escherichia coli"
+BMGC_DS05627,BMG_DS014768,Proteus meningitis
+BMGC_DS05628,BMG_DS014785,"Encephalitis, Acute Necrotizing"
+BMGC_DS05629,BMG_DS014794,Limbic Encephalitis
+BMGC_DS05630,BMG_DS014799,Neurocysticercosis
+BMGC_DS05631,BMG_DS014809,Frontotemporal dementia
+BMGC_DS05632,BMG_DS014818,semantic dementia
+BMGC_DS05633,BMG_DS014822,"Tic Disorders, Vocal"
+BMGC_DS05634,BMG_DS014825,Neuroaxonal Dystrophies
+BMGC_DS05635,BMG_DS014827,Idiopathic Myoclonic Epilepsy
+BMGC_DS05636,BMG_DS014828,Symptomatic Myoclonic Epilepsy
+BMGC_DS05637,BMG_DS014829,Common Migraine
+BMGC_DS05638,BMG_DS014831,Migraine with Prolonged Aura
+BMGC_DS05639,BMG_DS014832,Familial Hemiplegic Migraine
+BMGC_DS05640,BMG_DS014833,Migraine Aura without Headache
+BMGC_DS05641,BMG_DS014835,Alternating hemiplegia of childhood
+BMGC_DS05642,BMG_DS014836,Status Migrainosus
+BMGC_DS05643,BMG_DS014838,"Sleep Apnea, Mixed Central and Obstructive"
+BMGC_DS05644,BMG_DS014844,Optic Nerve Hypoplasia
+BMGC_DS05645,BMG_DS014845,Septo-Optic Dysplasia
+BMGC_DS05646,BMG_DS014849,Optic Atrophy 1
+BMGC_DS05647,BMG_DS014873,Ulnar Neuritis
+BMGC_DS05648,BMG_DS014888,Cerebral venous sinus thrombosis
+BMGC_DS05649,BMG_DS014890,Sagittal Sinus Thrombosis
+BMGC_DS05650,BMG_DS014895,Sporadic Cerebral Amyloid Angiopathy
+BMGC_DS05651,BMG_DS014896,Dissection of carotid artery
+BMGC_DS05652,BMG_DS014902,transient global amnesia
+BMGC_DS05653,BMG_DS014905,Spastic cerebral palsy
+BMGC_DS05654,BMG_DS014923,"Catatonia, Organic"
+BMGC_DS05655,BMG_DS014943,mixed anxiety and depressive disorder
+BMGC_DS05656,BMG_DS014977,Blepharochalasis And Double Lip
+BMGC_DS05657,BMG_DS014984,eyelid melanoma
+BMGC_DS05658,BMG_DS014987,secondary lacrimal atrophy
+BMGC_DS05659,BMG_DS014988,lacrimal gland neoplasm
+BMGC_DS05660,BMG_DS014991,Acute inflammation of lacrimal passages
+BMGC_DS05661,BMG_DS014992,Acute lacrimal canaliculitis
+BMGC_DS05662,BMG_DS014999,Graves Ophthalmopathy
+BMGC_DS05663,BMG_DS015012,Fungal conjunctivitis
+BMGC_DS05664,BMG_DS015031,Neuropathic corneal ulcer
+BMGC_DS05665,BMG_DS015051,"Corneal dystrophy, Lattice type 3"
+BMGC_DS05666,BMG_DS015052,"Corneal Dystrophy, Juvenile Epithelial of Meesmann"
+BMGC_DS05667,BMG_DS015053,Reis-Bucklers' corneal dystrophy
+BMGC_DS05668,BMG_DS015055,Polymorphous corneal dystrophy
+BMGC_DS05669,BMG_DS015056,Acute hydrops keratoconus
+BMGC_DS05670,BMG_DS015058,Exposure keratoconjunctivitis
+BMGC_DS05671,BMG_DS015059,Neurotrophic keratitis
+BMGC_DS05672,BMG_DS015063,cornea neoplasm
+BMGC_DS05673,BMG_DS015071,Non-infectious anterior uveitis
+BMGC_DS05674,BMG_DS015072,Lens-induced iridocyclitis
+BMGC_DS05675,BMG_DS015077,ciliary body neoplasm
+BMGC_DS05676,BMG_DS015092,Peripheral focal choroiditis AND chorioretinitis
+BMGC_DS05677,BMG_DS015112,Partial central choroid dystrophy
+BMGC_DS05678,BMG_DS015117,degeneration of macula and posterior pole
+BMGC_DS05679,BMG_DS015118,Other retinal disorders
+BMGC_DS05680,BMG_DS015147,central retinal vein occlusion with macular edema
+BMGC_DS05681,BMG_DS015152,Vitelliform Macular Dystrophy
+BMGC_DS05682,BMG_DS015154,Leber Congenital Amaurosis
+BMGC_DS05683,BMG_DS015157,Usher syndrome type 2
+BMGC_DS05684,BMG_DS015158,congenital stationary night blindness
+BMGC_DS05685,BMG_DS015159,blue cone monochromacy
+BMGC_DS05686,BMG_DS015160,Familial Exudative Vitreoretinopathies
+BMGC_DS05687,BMG_DS015161,Goldmann-Favre syndrome (disorder)
+BMGC_DS05688,BMG_DS015163,preretinal fibrosis
+BMGC_DS05689,BMG_DS015164,Retinal Pigment Epithelial Detachment
+BMGC_DS05690,BMG_DS015168,retina lymphoma
+BMGC_DS05691,BMG_DS015179,steroid-induced glaucoma - borderline
+BMGC_DS05692,BMG_DS015180,"Glaucoma, Primary Open Angle"
+BMGC_DS05693,BMG_DS015184,Corticosteroid-induced glaucoma
+BMGC_DS05694,BMG_DS015186,residual stage corticosteroid-induced glaucoma
+BMGC_DS05695,BMG_DS015197,Glaucoma due to ocular trauma
+BMGC_DS05696,BMG_DS015206,Monofixation syndrome
+BMGC_DS05697,BMG_DS015217,Primary Esotropia
+BMGC_DS05698,BMG_DS015218,Secondary Esotropia
+BMGC_DS05699,BMG_DS015262,Corneal Astigmatism
+BMGC_DS05700,BMG_DS015263,Lenticular Astigmatism
+BMGC_DS05701,BMG_DS015270,Anisometropic Amblyopia
+BMGC_DS05702,BMG_DS015274,"Blindness, Acquired"
+BMGC_DS05703,BMG_DS015283,Chronic otitis media with perforation
+BMGC_DS05704,BMG_DS015289,Congenital deafness
+BMGC_DS05705,BMG_DS015312,Disorder of nasal cavity
+BMGC_DS05706,BMG_DS015331,"nasal bones, absence of"
+BMGC_DS05707,BMG_DS015357,Lung disease with systemic sclerosis
+BMGC_DS05708,BMG_DS015375,Acute Moraxella catarrhalis bronchitis
+BMGC_DS05709,BMG_DS015376,Acute bacterial bronchitis
+BMGC_DS05710,BMG_DS015383,Pulmonary tularemia
+BMGC_DS05711,BMG_DS015390,Chlamydial pneumonia
+BMGC_DS05712,BMG_DS015399,Neonatal pneumonia
+BMGC_DS05713,BMG_DS015411,Idiopathic bronchiectasis
+BMGC_DS05714,BMG_DS015432,congenital chylothorax
+BMGC_DS05715,BMG_DS015448,"Immotile cilia syndrome, due to defective radial spokes"
+BMGC_DS05716,BMG_DS015450,Young Syndrome
+BMGC_DS05717,BMG_DS015451,Ciliary Discoordination Due To Random Ciliary Orientation
+BMGC_DS05718,BMG_DS015455,Acute exacerbation of chronic obstructive pulmonary disease
+BMGC_DS05719,BMG_DS015469,Hyperreactive airway disease
+BMGC_DS05720,BMG_DS015491,Summer-Type Hypersensitivity Pneumonitis
+BMGC_DS05721,BMG_DS015498,High altitude pulmonary edema
+BMGC_DS05722,BMG_DS015517,Localized pulmonary fibrosis
+BMGC_DS05723,BMG_DS015555,Baritosis
+BMGC_DS05724,BMG_DS015562,Mixed mineral dust pneumoconiosis
+BMGC_DS05725,BMG_DS015564,Schistosis
+BMGC_DS05726,BMG_DS015571,Hypoxemic Respiratory Failure
+BMGC_DS05727,BMG_DS015619,Ventricular hypertrophy
+BMGC_DS05728,BMG_DS015623,Stable angina
+BMGC_DS05729,BMG_DS015634,Inferior Wall Myocardial Infarction
+BMGC_DS05730,BMG_DS015641,lateral myocardial infarction
+BMGC_DS05731,BMG_DS015648,posterior myocardial infarction
+BMGC_DS05732,BMG_DS015649,Silent myocardial infarction
+BMGC_DS05733,BMG_DS015662,Q fever endocarditis
+BMGC_DS05734,BMG_DS015670,familial mitral valve prolapse
+BMGC_DS05735,BMG_DS015678,Subaortic stenosis
+BMGC_DS05736,BMG_DS015707,Familial dilated cardiomyopathy
+BMGC_DS05737,BMG_DS015709,familial restrictive cardiomyopathy
+BMGC_DS05738,BMG_DS015730,Premature Cardiac Complex
+BMGC_DS05739,BMG_DS015744,Familial Polymorphic Ventricular Tachycardia
+BMGC_DS05740,BMG_DS015750,Familial sick sinus syndrome
+BMGC_DS05741,BMG_DS015751,Paroxysmal familial ventricular fibrillation
+BMGC_DS05742,BMG_DS015752,Other conduction disorders
+BMGC_DS05743,BMG_DS015755,"Bundle Branch Block, Familial Isolated Complete Right"
+BMGC_DS05744,BMG_DS015773,Familial primary pulmonary hypertension
+BMGC_DS05745,BMG_DS015774,Pulmonary arterial hypertension induced by drug
+BMGC_DS05746,BMG_DS015777,Pulmonary capillary hemangiomatosis
+BMGC_DS05747,BMG_DS015781,High altitude pulmonary hypertension
+BMGC_DS05748,BMG_DS015791,Internal Carotid Artery Stenosis
+BMGC_DS05749,BMG_DS015806,Thrombosis of renal artery
+BMGC_DS05750,BMG_DS015813,Anterior Spinal Artery Dissection
+BMGC_DS05751,BMG_DS015814,Dissection of aorta
+BMGC_DS05752,BMG_DS015898,capillary malformation
+BMGC_DS05753,BMG_DS015899,Hereditary vascular fragility
+BMGC_DS05754,BMG_DS015900,splenoportal vascular anomalies
+BMGC_DS05755,BMG_DS015901,Hennekam lymphangiectasia-lymphedema syndrome
+BMGC_DS05756,BMG_DS015903,"PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE"
+BMGC_DS05757,BMG_DS015907,"Syncope, Situational"
+BMGC_DS05758,BMG_DS015908,"Syncope, Micturition"
+BMGC_DS05759,BMG_DS015981,Deficiency of pyruvate kinase
+BMGC_DS05760,BMG_DS015997,Odontoclasia
+BMGC_DS05761,BMG_DS016006,Streptococcal infection of mouth
+BMGC_DS05762,BMG_DS016013,Familial chronic mucocutaneous candidiasis
+BMGC_DS05763,BMG_DS016038,Eosinophilic esophagitis
+BMGC_DS05764,BMG_DS016040,Bacterial esophagitis
+BMGC_DS05765,BMG_DS016041,Fungal esophagitis
+BMGC_DS05766,BMG_DS016042,Viral esophagitis
+BMGC_DS05767,BMG_DS016065,"Esophageal Ring, Lower"
+BMGC_DS05768,BMG_DS016182,Microvillus inclusion disease
+BMGC_DS05769,BMG_DS016197,Indeterminate colitis
+BMGC_DS05770,BMG_DS016200,Cytomegalovirus Colitis
+BMGC_DS05771,BMG_DS016274,pancreatic cystadenoma
+BMGC_DS05772,BMG_DS016284,Bacterial peritonitis
+BMGC_DS05773,BMG_DS016299,Intestinal infection caused by Escherichia coli
+BMGC_DS05774,BMG_DS016339,impaired renal function disease
+BMGC_DS05775,BMG_DS016347,Acute diffuse nephritis
+BMGC_DS05776,BMG_DS016350,Acute proliferative glomerulonephritis
+BMGC_DS05777,BMG_DS016352,chronic rapidly progressive glomerulonephritis
+BMGC_DS05778,BMG_DS016353,Atrophy of kidney
+BMGC_DS05779,BMG_DS016356,Adult Fanconi syndrome
+BMGC_DS05780,BMG_DS016370,Detrusor and sphincter dyssynergia
+BMGC_DS05781,BMG_DS016378,paraurethral gland neoplasm
+BMGC_DS05782,BMG_DS016379,seminal vesicle tumor
+BMGC_DS05783,BMG_DS016386,Chlamydial epididymitis
+BMGC_DS05784,BMG_DS016390,scrotum neoplasm
+BMGC_DS05785,BMG_DS016406,ovarian epithelial tumor
+BMGC_DS05786,BMG_DS016421,Endometriosis of uterus
+BMGC_DS05787,BMG_DS016427,"Subfertility, Female"
+BMGC_DS05788,BMG_DS016464,severe pre-eclampsia
+BMGC_DS05789,BMG_DS016537,Toxic nodular goiter
+BMGC_DS05790,BMG_DS016556,Congenital hypothyroidism without goiter
+BMGC_DS05791,BMG_DS016559,"Hypothyroidism, Autoimmune"
+BMGC_DS05792,BMG_DS016577,"Hyperthyroxinemia, Familial Dysalbuminemic"
+BMGC_DS05793,BMG_DS016580,C-cell hyperplasia of thyroid
+BMGC_DS05794,BMG_DS016584,Thyroid Dyshormonogenesis 3
+BMGC_DS05795,BMG_DS016585,Thyroid Dyshormonogenesis 4
+BMGC_DS05796,BMG_DS016586,Thyroid Dyshormonogenesis 5
+BMGC_DS05797,BMG_DS016588,Iodine deficiency syndrome
+BMGC_DS05798,BMG_DS016589,Endemic Cretinism
+BMGC_DS05799,BMG_DS016610,Complications of Diabetes Mellitus
+BMGC_DS05800,BMG_DS016620,Transitory neonatal diabetes mellitus
+BMGC_DS05801,BMG_DS016622,Maturity onset diabetes mellitus in young
+BMGC_DS05802,BMG_DS016623,Diabetes mellitus autosomal dominant type II (disorder)
+BMGC_DS05803,BMG_DS016624,Hereditary benign acanthosis nigricans with insulin resistance
+BMGC_DS05804,BMG_DS016625,AREDYLD Syndrome
+BMGC_DS05805,BMG_DS016626,"Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus"
+BMGC_DS05806,BMG_DS016627,Multiple synostoses syndrome 1
+BMGC_DS05807,BMG_DS016628,Hyperproinsulinemia
+BMGC_DS05808,BMG_DS016629,Bangstad syndrome
+BMGC_DS05809,BMG_DS016630,Woodhouse Sakati syndrome
+BMGC_DS05810,BMG_DS016631,thiamine-responsive megaloblastic anemia syndrome
+BMGC_DS05811,BMG_DS016632,Insulin-dependent diabetes mellitus secretory diarrhea syndrome
+BMGC_DS05812,BMG_DS016633,Diabetes-deafness syndrome maternally transmitted
+BMGC_DS05813,BMG_DS016650,Hypoglycemia due to diabetes mellitus
+BMGC_DS05814,BMG_DS016663,Insulin resistance - type A
+BMGC_DS05815,BMG_DS016668,Idiopathic Hypoparathyroidism
+BMGC_DS05816,BMG_DS016669,Hypoparathyroidism - X-linked
+BMGC_DS05817,BMG_DS016670,Hypoparathyroidism - autosomal dominant
+BMGC_DS05818,BMG_DS016680,Panhypopituitarism - X-linked
+BMGC_DS05819,BMG_DS016683,Idiopathic growth hormone deficiency
+BMGC_DS05820,BMG_DS016685,Idiopathic hypogonadotropic hypogonadism
+BMGC_DS05821,BMG_DS016688,Adrenocorticotropic hormone (ACTH) deficiency (disorder)
+BMGC_DS05822,BMG_DS016689,Familial vasopressin deficiency
+BMGC_DS05823,BMG_DS016698,Pituitary infarction
+BMGC_DS05824,BMG_DS016707,congenital hypothalamic hamartoma syndrome
+BMGC_DS05825,BMG_DS016734,3 beta-Hydroxysteroid dehydrogenase deficiency
+BMGC_DS05826,BMG_DS016735,17 alpha-Hydroxyprogesterone aldolase deficiency
+BMGC_DS05827,BMG_DS016736,Lipoid congenital adrenal hyperplasia
+BMGC_DS05828,BMG_DS016740,X-linked Adrenal Hypoplasia
+BMGC_DS05829,BMG_DS016743,"Mineralocorticoid Excess Syndrome, Apparent"
+BMGC_DS05830,BMG_DS016747,Macronodular adrenal hyperplasia
+BMGC_DS05831,BMG_DS016766,Deficiency of testosterone biosynthesis
+BMGC_DS05832,BMG_DS016777,Central Precocious Puberty
+BMGC_DS05833,BMG_DS016781,Familial Testotoxicosis
+BMGC_DS05834,BMG_DS016788,Carcinoid crisis
+BMGC_DS05835,BMG_DS016790,isolated growth hormone deficiency type IA
+BMGC_DS05836,BMG_DS016799,"Amyloid Polyneuropathy, British Type"
+BMGC_DS05837,BMG_DS016801,Familial non-neuropathic amyloidosis
+BMGC_DS05838,BMG_DS016812,Neonatal hypocalcemia
+BMGC_DS05839,BMG_DS016815,"Hypocalciuric hypercalcemia, familial, type 1"
+BMGC_DS05840,BMG_DS016817,"hypercalciuria, absorptive, 2"
+BMGC_DS05841,BMG_DS016819,Autosomal dominant hypophosphatemic rickets
+BMGC_DS05842,BMG_DS016820,Autosomal recessive hypophosphatemic vitamin D refractory rickets
+BMGC_DS05843,BMG_DS016821,"Vitamin D-Dependent Rickets, Type 2A"
+BMGC_DS05844,BMG_DS016823,Vascular calcification
+BMGC_DS05845,BMG_DS016838,"ALBINISM, OCULOCUTANEOUS, TYPE III"
+BMGC_DS05846,BMG_DS016839,"Ocular albinism, type I"
+BMGC_DS05847,BMG_DS016842,dopamine beta hydroxylase deficiency
+BMGC_DS05848,BMG_DS016849,Transcobalamin I Deficiency
+BMGC_DS05849,BMG_DS016850,Transcobalamin II deficiency
+BMGC_DS05850,BMG_DS016854,"Folate Malabsorption, Hereditary"
+BMGC_DS05851,BMG_DS016856,Gamma aminobutyric acid transaminase deficiency
+BMGC_DS05852,BMG_DS016864,Complete deficiency of methylmalonyl-CoA mutase
+BMGC_DS05853,BMG_DS016865,Partial deficiency of methylmalonyl-CoA mutase
+BMGC_DS05854,BMG_DS016870,"3-@METHYLGLUTACONIC ACIDURIA, TYPE I"
+BMGC_DS05855,BMG_DS016872,Deficiency of mevalonate kinase
+BMGC_DS05856,BMG_DS016874,Cytosolic acetoacetyl-CoA thiolase deficiency
+BMGC_DS05857,BMG_DS016875,3-Hydroxyisobutyric aciduria
+BMGC_DS05858,BMG_DS016876,Beta-Hydroxyisobutyryl CoA Deacylase Deficiency
+BMGC_DS05859,BMG_DS016877,Trimethylaminuria
+BMGC_DS05860,BMG_DS016884,GLYCOGEN STORAGE DISEASE Ic
+BMGC_DS05861,BMG_DS016886,Generalized glycogen storage disease of infants
+BMGC_DS05862,BMG_DS016888,Glycogen storage disease type II late onset
+BMGC_DS05863,BMG_DS016898,D-Glyceric aciduria
+BMGC_DS05864,BMG_DS016901,Fumarase deficiency
+BMGC_DS05865,BMG_DS016907,Depletion of mitochondrial DNA
+BMGC_DS05866,BMG_DS016908,Deficiency of butyryl-CoA dehydrogenase
+BMGC_DS05867,BMG_DS016909,Pearson's marrow-pancreas syndrome
+BMGC_DS05868,BMG_DS016912,Renal carnitine transport defect
+BMGC_DS05869,BMG_DS016913,Carnitine palmitoyl transferase 2 deficiency
+BMGC_DS05870,BMG_DS016914,Carnitine-Acylcarnitine Translocase Deficiency
+BMGC_DS05871,BMG_DS016915,Succinyl-CoA:3-oxoacid CoA transferase deficiency
+BMGC_DS05872,BMG_DS016916,Malonic aciduria
+BMGC_DS05873,BMG_DS016919,Inosine Triphosphatase Deficiency
+BMGC_DS05874,BMG_DS016920,Thiopurine S methyltranferase deficiency
+BMGC_DS05875,BMG_DS016922,Dihydropyrimidinase deficiency
+BMGC_DS05876,BMG_DS016943,"Hunter's syndrome, severe form"
+BMGC_DS05877,BMG_DS016944,"Hunter's syndrome, mild form"
+BMGC_DS05878,BMG_DS016947,"Mannosidosis, type I"
+BMGC_DS05879,BMG_DS016950,Sialuria
+BMGC_DS05880,BMG_DS016952,Coproporphyria
+BMGC_DS05881,BMG_DS016955,Harderoporphyria
+BMGC_DS05882,BMG_DS016960,d-bifunctional protein deficiency
+BMGC_DS05883,BMG_DS016962,Glutaric Aciduria III
+BMGC_DS05884,BMG_DS016968,Homozygous Familial Hypercholesterolemia
+BMGC_DS05885,BMG_DS016969,Familial hypercholesterolemia - heterozygous
+BMGC_DS05886,BMG_DS016970,Cholesteryl Ester Transfer Protein Deficiency
+BMGC_DS05887,BMG_DS016975,Fish-Eye Disease
+BMGC_DS05888,BMG_DS016976,Apolipoprotein A-I deficiency
+BMGC_DS05889,BMG_DS016978,sitosterolemia
+BMGC_DS05890,BMG_DS016988,Pantothenic acid deficiency
+BMGC_DS05891,BMG_DS017012,Superficial bacterial infection of skin
+BMGC_DS05892,BMG_DS017036,Complement component 5 deficiency
+BMGC_DS05893,BMG_DS017039,Guttate Psoriasis
+BMGC_DS05894,BMG_DS017041,Generalized pustular psoriasis
+BMGC_DS05895,BMG_DS017042,keratosis follicularis spinulosa decalvans
+BMGC_DS05896,BMG_DS017045,Dermatographic urticaria
+BMGC_DS05897,BMG_DS017046,Familial cold urticaria
+BMGC_DS05898,BMG_DS017049,isolated familial wooly hair disorder
+BMGC_DS05899,BMG_DS017055,"milia, multiple eruptive"
+BMGC_DS05900,BMG_DS017057,Livedoid vasculitis
+BMGC_DS05901,BMG_DS017058,cherry hemangioma
+BMGC_DS05902,BMG_DS017060,Capillary Leak Syndrome
+BMGC_DS05903,BMG_DS017062,"hereditary sclerosing poikiloderma, Weary type"
+BMGC_DS05904,BMG_DS017063,Nodular Elastoidosis
+BMGC_DS05905,BMG_DS017067,Flynn Aird syndrome
+BMGC_DS05906,BMG_DS017068,Naegeli syndrome
+BMGC_DS05907,BMG_DS017070,wooly hair nevus
+BMGC_DS05908,BMG_DS017071,cutaneous mastocytoma
+BMGC_DS05909,BMG_DS017092,Cutaneous polyarteritis nodosa
+BMGC_DS05910,BMG_DS017103,Systemic rheumatoid vasculitis
+BMGC_DS05911,BMG_DS017106,Hypocomplementemic urticarial vasculitis
+BMGC_DS05912,BMG_DS017150,chondrodysplasia
+BMGC_DS05913,BMG_DS017158,Tetanus neonatorum
+BMGC_DS05914,BMG_DS017175,Pseudomonas gastrointestinal tract infection
+BMGC_DS05915,BMG_DS017201,Helicobacter-associated gastritis
+BMGC_DS05916,BMG_DS017208,Clostridium difficile infection
+BMGC_DS05917,BMG_DS017218,Cyclosporiasis
+BMGC_DS05918,BMG_DS017221,Methicillin resistant Staphylococcus aureus infection
+BMGC_DS05919,BMG_DS017222,Bacterial infection caused by Klebsiella pneumoniae
+BMGC_DS05920,BMG_DS017270,Erythema nodosum leprosum
+BMGC_DS05921,BMG_DS017285,Streptococcal sore throat with scarlatina
+BMGC_DS05922,BMG_DS017296,Gas gangrene caused by clostridium perfringens
+BMGC_DS05923,BMG_DS017322,Pontiac Fever
+BMGC_DS05924,BMG_DS017325,Streptococcal toxic shock syndrome
+BMGC_DS05925,BMG_DS017417,Human papilloma virus infection
+BMGC_DS05926,BMG_DS017469,Gonococcal synovitis or tenosynovitis
+BMGC_DS05927,BMG_DS017482,Perianal warts
+BMGC_DS05928,BMG_DS017498,Acute HIV infection
+BMGC_DS05929,BMG_DS017500,HIV Wasting Syndrome
+BMGC_DS05930,BMG_DS017503,American tick typhus
+BMGC_DS05931,BMG_DS017559,Tertiary lesion of yaws
+BMGC_DS05932,BMG_DS017560,Bone and/or joint yaws lesions
+BMGC_DS05933,BMG_DS017580,Pharyngeal candidiasis
+BMGC_DS05934,BMG_DS017602,Gastrointestinal candidiasis
+BMGC_DS05935,BMG_DS017646,Trichosporonosis
+BMGC_DS05936,BMG_DS017647,Disseminated Trichosporonosis
+BMGC_DS05937,BMG_DS017666,Entomophthoramycosis
+BMGC_DS05938,BMG_DS017792,See-Saw Nystagmus
+BMGC_DS05939,BMG_DS017802,Bullous retinoschisis
+BMGC_DS05940,BMG_DS017803,Vitreoretinal degeneration
+BMGC_DS05941,BMG_DS017805,Choroidal sclerosis
+BMGC_DS05942,BMG_DS017808,flying phobia
+BMGC_DS05943,BMG_DS017824,"Ventricular tachycardia, polymorphic"
+BMGC_DS05944,BMG_DS017826,adrenal medulla cancer
+BMGC_DS05945,BMG_DS017827,carcinoma ex pleomorphic adenoma
+BMGC_DS05946,BMG_DS017829,Spinal intradural arachnoid cysts
+BMGC_DS05947,BMG_DS017833,coloboma of eye lens
+BMGC_DS05948,BMG_DS017834,cerulean cataract
+BMGC_DS05949,BMG_DS017836,cornea plana
+BMGC_DS05950,BMG_DS017837,megalocornea
+BMGC_DS05951,BMG_DS017838,aniridia 1
+BMGC_DS05952,BMG_DS017839,aniridia 2
+BMGC_DS05953,BMG_DS017841,Peters anomaly
+BMGC_DS05954,BMG_DS017851,patent ductus venosus
+BMGC_DS05955,BMG_DS017853,cor triatriatum dexter
+BMGC_DS05956,BMG_DS017859,"atrial septal defect, ostium secundum type"
+BMGC_DS05957,BMG_DS017860,"atrial septal defect, sinus venosus type"
+BMGC_DS05958,BMG_DS017863,mitral atresia disorder
+BMGC_DS05959,BMG_DS017879,Left cardiac ventricular dilatation
+BMGC_DS05960,BMG_DS017883,Right hypoplastic heart syndrome
+BMGC_DS05961,BMG_DS017884,pulmonary atresia-intact ventricular septum syndrome
+BMGC_DS05962,BMG_DS017885,pulmonary atresia with ventricular septal defect
+BMGC_DS05963,BMG_DS017889,aorta atresia
+BMGC_DS05964,BMG_DS017891,Peripheral pulmonary artery stenosis
+BMGC_DS05965,BMG_DS017894,"aortic aneurysm, familial thoracic 1"
+BMGC_DS05966,BMG_DS017905,laryngomalacia
+BMGC_DS05967,BMG_DS017916,"aganglionosis, total intestinal"
+BMGC_DS05968,BMG_DS017923,phimosis
+BMGC_DS05969,BMG_DS017925,atresia of urethra
+BMGC_DS05970,BMG_DS017929,femoral agenesis/hypoplasia
+BMGC_DS05971,BMG_DS017931,"OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3"
+BMGC_DS05972,BMG_DS017932,isolated congenital digital clubbing
+BMGC_DS05973,BMG_DS017933,cutis marmorata telangiectatica congenita
+BMGC_DS05974,BMG_DS017934,"comedones, familial Dyskeratotic"
+BMGC_DS05975,BMG_DS017949,neoplasm of middle ear
+BMGC_DS05976,BMG_DS017952,ethmoidal sinus neoplasm
+BMGC_DS05977,BMG_DS017954,frontal sinus neoplasm
+BMGC_DS05978,BMG_DS017956,sphenoidal sinus neoplasm
+BMGC_DS05979,BMG_DS017958,glottis neoplasm
+BMGC_DS05980,BMG_DS017959,supraglottis neoplasm
+BMGC_DS05981,BMG_DS017960,subglottis neoplasm
+BMGC_DS05982,BMG_DS017963,gastric fundus carcinoma
+BMGC_DS05983,BMG_DS017965,gastric body carcinoma
+BMGC_DS05984,BMG_DS017967,small intestine neoplasm
+BMGC_DS05985,BMG_DS017970,rectosigmoid junction neoplasm
+BMGC_DS05986,BMG_DS017972,juvenile polyposis syndrome
+BMGC_DS05987,BMG_DS017974,liver cancer
+BMGC_DS05988,BMG_DS017975,intrahepatic cholangiocarcinoma
+BMGC_DS05989,BMG_DS017976,liver sarcoma
+BMGC_DS05990,BMG_DS017977,liver angiosarcoma
+BMGC_DS05991,BMG_DS017981,extrahepatic bile duct neoplasm
+BMGC_DS05992,BMG_DS017983,ampulla of vater neoplasm
+BMGC_DS05993,BMG_DS017986,tracheal adenoid cystic carcinoma
+BMGC_DS05994,BMG_DS017987,trachea squamous cell carcinoma
+BMGC_DS05995,BMG_DS017988,lung large cell carcinoma
+BMGC_DS05996,BMG_DS017989,lung clear cell carcinoma
+BMGC_DS05997,BMG_DS017990,lung giant cell carcinoma
+BMGC_DS05998,BMG_DS017992,lung adenoma
+BMGC_DS05999,BMG_DS017993,malignant mesothelioma
+BMGC_DS06000,BMG_DS017996,clear cell squamous cell skin carcinoma
+BMGC_DS06001,BMG_DS017997,acantholytic squamous cell skin carcinoma
+BMGC_DS06002,BMG_DS017999,Ferguson-Smith tumor
+BMGC_DS06003,BMG_DS018000,squamous cell skin papilloma
+BMGC_DS06004,BMG_DS018002,epidermal appendage tumor
+BMGC_DS06005,BMG_DS018006,pilar sheath acanthoma
+BMGC_DS06006,BMG_DS018007,follicular infundibulum tumor
+BMGC_DS06007,BMG_DS018008,Birt-Hogg-Dube Syndrome
+BMGC_DS06008,BMG_DS018009,skin fibroepithelial basal cell carcinoma
+BMGC_DS06009,BMG_DS018010,cutaneous adenocystic carcinoma
+BMGC_DS06010,BMG_DS018011,cutaneous mucoepidermoid carcinoma
+BMGC_DS06011,BMG_DS018013,eccrine mixed tumor of skin
+BMGC_DS06012,BMG_DS018016,dermis tumor
+BMGC_DS06013,BMG_DS018017,cutaneous fibrous histiocytoma
+BMGC_DS06014,BMG_DS018018,verruciform xanthoma of skin
+BMGC_DS06015,BMG_DS018020,cutaneous granular cell tumor
+BMGC_DS06016,BMG_DS018021,cutaneous ganglioneuroma
+BMGC_DS06017,BMG_DS018022,leiomyoma cutis
+BMGC_DS06018,BMG_DS018024,cutaneous leiomyosarcoma
+BMGC_DS06019,BMG_DS018026,blue rubber bleb nevus
+BMGC_DS06020,BMG_DS018027,tufted angioma
+BMGC_DS06021,BMG_DS018028,angiokeratoma
+BMGC_DS06022,BMG_DS018030,skin angiosarcoma
+BMGC_DS06023,BMG_DS018032,skin glomus tumor
+BMGC_DS06024,BMG_DS018036,Bazex-Dupre-Christol syndrome
+BMGC_DS06025,BMG_DS018037,malignant peritoneal mesothelioma
+BMGC_DS06026,BMG_DS018038,pericardial mesothelioma
+BMGC_DS06027,BMG_DS018041,benign lipomatous neoplasm
+BMGC_DS06028,BMG_DS018042,scirrhous breast carcinoma
+BMGC_DS06029,BMG_DS018043,hereditary breast carcinoma
+BMGC_DS06030,BMG_DS018044,malignant breast phyllodes tumor
+BMGC_DS06031,BMG_DS018046,breast giant fibroadenoma
+BMGC_DS06032,BMG_DS018047,breast fibroadenoma
+BMGC_DS06033,BMG_DS018048,malignant epithelial tumor of ovary
+BMGC_DS06034,BMG_DS018049,ovarian endometrioid adenocarcinoma
+BMGC_DS06035,BMG_DS018052,undifferentiated ovarian carcinoma
+BMGC_DS06036,BMG_DS018053,ovarian cystadenoma
+BMGC_DS06037,BMG_DS018054,mucinous ovarian cystadenoma
+BMGC_DS06038,BMG_DS018057,malignant germ cell tumor of ovary
+BMGC_DS06039,BMG_DS018058,choriocarcinoma of ovary
+BMGC_DS06040,BMG_DS018059,immature ovarian teratoma
+BMGC_DS06041,BMG_DS018060,ovarian embryonal carcinoma
+BMGC_DS06042,BMG_DS018061,dysgerminoma of ovary
+BMGC_DS06043,BMG_DS018062,ovarian yolk sac tumor
+BMGC_DS06044,BMG_DS018064,endometrium carcinoma in situ
+BMGC_DS06045,BMG_DS018065,intravenous leiomyomatosis
+BMGC_DS06046,BMG_DS018066,cervical adenosquamous carcinoma
+BMGC_DS06047,BMG_DS018069,epididymal neoplasm
+BMGC_DS06048,BMG_DS018070,multilocular clear cell renal cell carcinoma
+BMGC_DS06049,BMG_DS018071,kidney sarcoma
+BMGC_DS06050,BMG_DS018072,kidney oncocytoma
+BMGC_DS06051,BMG_DS018073,kidney hemangiopericytoma
+BMGC_DS06052,BMG_DS018074,renal pelvis neoplasm
+BMGC_DS06053,BMG_DS018077,choroid plexus cancer
+BMGC_DS06054,BMG_DS018079,spinal cord oligodendroglioma
+BMGC_DS06055,BMG_DS018080,pituitary adenocarcinoma
+BMGC_DS06056,BMG_DS018081,growth hormone secreting pituitary adenoma
+BMGC_DS06057,BMG_DS018082,TSH-secreting pituitary adenoma
+BMGC_DS06058,BMG_DS018086,optic nerve glioma
+BMGC_DS06059,BMG_DS018087,optic nerve sheath meningioma
+BMGC_DS06060,BMG_DS018089,malignant neoplasm of acoustic nerve
+BMGC_DS06061,BMG_DS018090,lacrimal gland adenoid cystic carcinoma
+BMGC_DS06062,BMG_DS018091,lacrimal gland adenocarcinoma
+BMGC_DS06063,BMG_DS018092,lacrimal gland carcinoma ex pleomorphic adenoma
+BMGC_DS06064,BMG_DS018093,orbit rhabdomyosarcoma
+BMGC_DS06065,BMG_DS018094,cavernous hemangioma of orbit
+BMGC_DS06066,BMG_DS018095,conjunctival squamous cell carcinoma
+BMGC_DS06067,BMG_DS018096,malignant conjunctival melanoma
+BMGC_DS06068,BMG_DS018098,cornea squamous cell carcinoma
+BMGC_DS06069,BMG_DS018099,malignant cornea melanoma
+BMGC_DS06070,BMG_DS018100,iris cancer
+BMGC_DS06071,BMG_DS018101,iris melanoma
+BMGC_DS06072,BMG_DS018103,malignant ciliary body melanoma
+BMGC_DS06073,BMG_DS018105,malignant choroid melanoma
+BMGC_DS06074,BMG_DS018107,malignant tumor of adrenal cortex
+BMGC_DS06075,BMG_DS018110,chronic eosinophilic leukemia
+BMGC_DS06076,BMG_DS018111,spleen angiosarcoma
+BMGC_DS06077,BMG_DS018113,lung hilum cancer
+BMGC_DS06078,BMG_DS018114,pericardium cancer
+BMGC_DS06079,BMG_DS018115,epicardium cancer
+BMGC_DS06080,BMG_DS018116,myocardium cancer
+BMGC_DS06081,BMG_DS018117,endocardium cancer
+BMGC_DS06082,BMG_DS018118,gastroesophageal cancer
+BMGC_DS06083,BMG_DS018119,intestinal cancer
+BMGC_DS06084,BMG_DS018120,colorectal cancer
+BMGC_DS06085,BMG_DS018121,malignant exocrine pancreas neoplasm
+BMGC_DS06086,BMG_DS018122,malignant breast melanoma
+BMGC_DS06087,BMG_DS018123,malignant dermis tumor
+BMGC_DS06088,BMG_DS018124,vascular cancer
+BMGC_DS06089,BMG_DS018125,broad ligament malignant neoplasm
+BMGC_DS06090,BMG_DS018126,round ligament malignant neoplasm
+BMGC_DS06091,BMG_DS018127,thalamic cancer
+BMGC_DS06092,BMG_DS018129,cerebral ventricle cancer
+BMGC_DS06093,BMG_DS018130,Kaposi's sarcoma
+BMGC_DS06094,BMG_DS018131,Kaposi's sarcoma
+BMGC_DS06095,BMG_DS018132,malignant neoplasm of chest wall
+BMGC_DS06096,BMG_DS018133,metastatic malignant neoplasm in the colon
+BMGC_DS06097,BMG_DS018138,nasal cavity carcinoma in situ
+BMGC_DS06098,BMG_DS018146,skin carcinoma in situ
+BMGC_DS06099,BMG_DS018153,benign neoplasm of nasal cavity
+BMGC_DS06100,BMG_DS018160,benign neoplasm of large intestine
+BMGC_DS06101,BMG_DS018166,skin papilloma
+BMGC_DS06102,BMG_DS018167,skin lipoma
+BMGC_DS06103,BMG_DS018172,spinal cord lipoma
+BMGC_DS06104,BMG_DS018177,spinal meningioma
+BMGC_DS06105,BMG_DS018194,"Epilepsy, Akinetic"
+BMGC_DS06106,BMG_DS018223,Congenital malformation syndromes associated with short stature
+BMGC_DS06107,BMG_DS018225,Non-Syphilitic Argyll-Robertson Pupil
+BMGC_DS06108,BMG_DS018229,Asthma attack
+BMGC_DS06109,BMG_DS018352,bronchus cancer
+BMGC_DS06110,BMG_DS018353,urinary system cancer
+BMGC_DS06111,BMG_DS018354,central nervous system cancer
+BMGC_DS06112,BMG_DS018363,Other hypoparathyroidism
+BMGC_DS06113,BMG_DS018365,Other disorders of pituitary gland
+BMGC_DS06114,BMG_DS018368,Other hyperaldosteronism
+BMGC_DS06115,BMG_DS018379,Other disorders of branched-chain amino-acid metabolism
+BMGC_DS06116,BMG_DS018384,Other sphingolipidosis
+BMGC_DS06117,BMG_DS018443,Other cardiomyopathies
+BMGC_DS06118,BMG_DS018446,Other specified cardiac arrhythmias
+BMGC_DS06119,BMG_DS018518,Other specified diseases of liver
+BMGC_DS06120,BMG_DS018582,Listerial endocarditis
+BMGC_DS06121,BMG_DS018590,"Aplastic anemia, idiopathic"
+BMGC_DS06122,BMG_DS018595,Irritable bowel syndrome with diarrhea
+BMGC_DS06123,BMG_DS018617,Other specified diabetes mellitus with unspecified complications
+BMGC_DS06124,BMG_DS018663,Cerebral Cryptococcosis
+BMGC_DS06125,BMG_DS018683,phobic disorder
+BMGC_DS06126,BMG_DS018684,Nonorganic Insomnia
+BMGC_DS06127,BMG_DS018713,Wernicke-Korsakoff syndrome
+BMGC_DS06128,BMG_DS018726,Fetal Hypoxia
+BMGC_DS06129,BMG_DS018736,dermoid cyst of skin
+BMGC_DS06130,BMG_DS018737,skin sensitivity to sun
+BMGC_DS06131,BMG_DS018740,amelanotic skin melanoma
+BMGC_DS06132,BMG_DS018750,microinvasive gastric cancer
+BMGC_DS06133,BMG_DS018751,gastric lymphoma
+BMGC_DS06134,BMG_DS018752,anal margin carcinoma
+BMGC_DS06135,BMG_DS018753,intestinal neuroendocrine tumor G1
+BMGC_DS06136,BMG_DS018755,anal melanoma
+BMGC_DS06137,BMG_DS018756,rectum malignant melanoma
+BMGC_DS06138,BMG_DS018757,spinal cord astrocytoma
+BMGC_DS06139,BMG_DS018758,brain glioblastoma
+BMGC_DS06140,BMG_DS018759,scrotum squamous cell carcinoma
+BMGC_DS06141,BMG_DS018761,gestational choriocarcinoma
+BMGC_DS06142,BMG_DS018762,bartholin gland carcinoma
+BMGC_DS06143,BMG_DS018765,tongue squamous cell carcinoma
+BMGC_DS06144,BMG_DS018766,neoplasm of pericardium
+BMGC_DS06145,BMG_DS018768,external ear cancer
+BMGC_DS06146,BMG_DS018769,Complex Endometrial Hyperplasia
+BMGC_DS06147,BMG_DS018770,Atypical Endometrial Hyperplasia
+BMGC_DS06148,BMG_DS018771,trigeminal schwannoma
+BMGC_DS06149,BMG_DS018775,intracranial meningioma
+BMGC_DS06150,BMG_DS018776,Central Nervous System Cysts
+BMGC_DS06151,BMG_DS018781,cerebellar pilocytic astrocytoma
+BMGC_DS06152,BMG_DS018782,malignant pineal area germ cell neoplasm
+BMGC_DS06153,BMG_DS018783,meninges hemangiopericytoma
+BMGC_DS06154,BMG_DS018784,central nervous system melanocytic neoplasm
+BMGC_DS06155,BMG_DS018787,Richter syndrome
+BMGC_DS06156,BMG_DS018789,hairy cell leukemia variant
+BMGC_DS06157,BMG_DS018790,precursor B-cell acute lymphoblastic leukemia
+BMGC_DS06158,BMG_DS018791,juvenile myelomonocytic leukemia
+BMGC_DS06159,BMG_DS018794,testicular lymphoma
+BMGC_DS06160,BMG_DS018795,lung lymphangioleiomyomatosis
+BMGC_DS06161,BMG_DS018796,Non-tuberculous mycobacterial pneumonia
+BMGC_DS06162,BMG_DS018797,Congenital disorder of glycosylation type 1A
+BMGC_DS06163,BMG_DS018798,"Congenital Disorder Of Glycosylation, Type I-IIX"
+BMGC_DS06164,BMG_DS018799,sarcomatoid squamous cell skin carcinoma
+BMGC_DS06165,BMG_DS018800,plantar verrucous skin carcinoma
+BMGC_DS06166,BMG_DS018805,bladder sarcoma
+BMGC_DS06167,BMG_DS018806,breast sarcoma
+BMGC_DS06168,BMG_DS018807,breast lymphoma
+BMGC_DS06169,BMG_DS018820,Hypoglossal Neuralgia
+BMGC_DS06170,BMG_DS018821,Herpes simplex infection of skin
+BMGC_DS06171,BMG_DS018825,Female pelvic cellulitis
+BMGC_DS06172,BMG_DS018839,Diverticulitis of gastrointestinal tract
+BMGC_DS06173,BMG_DS018843,Arrhythmogenic Right Ventricular Dysplasia
+BMGC_DS06174,BMG_DS018844,acute asthma
+BMGC_DS06175,BMG_DS018850,prediabetes syndrome
+BMGC_DS06176,BMG_DS018854,vulva cancer
+BMGC_DS06177,BMG_DS018856,anaerobic meningitis
+BMGC_DS06178,BMG_DS018857,Shuddering attacks
+BMGC_DS06179,BMG_DS018863,Acute endocarditis
+BMGC_DS06180,BMG_DS018864,carotid artery occlusion
+BMGC_DS06181,BMG_DS018867,Pneumonia due to other streptococci
+BMGC_DS06182,BMG_DS018868,anaerobic pneumonia
+BMGC_DS06183,BMG_DS018872,Chronic left-sided ulcerative colitis
+BMGC_DS06184,BMG_DS018879,Urethral intrinsic sphincter deficiency
+BMGC_DS06185,BMG_DS018881,pigmentation disease
+BMGC_DS06186,BMG_DS018883,inflamed seborrheic keratosis
+BMGC_DS06187,BMG_DS018884,Necrotizing Hemorrhagic Encephalomyelitis
+BMGC_DS06188,BMG_DS018885,Bell Palsy
+BMGC_DS06189,BMG_DS018886,"Hypoaldosteronism, Hyporeninemic"
+BMGC_DS06190,BMG_DS018888,Avitaminosis
+BMGC_DS06191,BMG_DS018889,Amaurosis
+BMGC_DS06192,BMG_DS018890,Dengue Shock Syndrome
+BMGC_DS06193,BMG_DS018892,congenital epulis
+BMGC_DS06194,BMG_DS018893,Congestive Ophthalmopathy
+BMGC_DS06195,BMG_DS018894,New Variant Creutzfeldt-Jakob Disease
+BMGC_DS06196,BMG_DS018895,Premenstrual Tension
+BMGC_DS06197,BMG_DS018896,prostate cancer
+BMGC_DS06198,BMG_DS018897,Gronblad-Strandberg Syndrome
+BMGC_DS06199,BMG_DS018898,Purpura Hemorrhagica
+BMGC_DS06200,BMG_DS018899,Posterior Cervical Sympathetic Syndrome
+BMGC_DS06201,BMG_DS018902,"Hibernation, Myocardial"
+BMGC_DS06202,BMG_DS018903,gingival overgrowth
+BMGC_DS06203,BMG_DS018904,Branchio-Oculo-Facial Syndrome
+BMGC_DS06204,BMG_DS018905,skull base neoplasm
+BMGC_DS06205,BMG_DS018906,"Epilepsy, Rolandic"
+BMGC_DS06206,BMG_DS018908,hematopoietic and lymphoid cell neoplasm
+BMGC_DS06207,BMG_DS018912,Endotoxemia
+BMGC_DS06208,BMG_DS018914,"Pancreatitis, Alcoholic"
+BMGC_DS06209,BMG_DS018915,Shoulder Impingement Syndrome
+BMGC_DS06210,BMG_DS018918,Clinical Capillary Leak Syndrome
+BMGC_DS06211,BMG_DS018919,Esophageal Hernia
+BMGC_DS06212,BMG_DS018921,Tietz syndrome
+BMGC_DS06213,BMG_DS018926,Lhermitte-Duclos disease
+BMGC_DS06214,BMG_DS018929,erythropoietin polycythemia
+BMGC_DS06215,BMG_DS018933,Cervical Sympathetic Dystrophy
+BMGC_DS06216,BMG_DS018944,Infarction of testis
+BMGC_DS06217,BMG_DS018947,Suppurative lymphadenopathy
+BMGC_DS06218,BMG_DS018953,Cardiac sarcoidosis
+BMGC_DS06219,BMG_DS018958,tracheomalacia
+BMGC_DS06220,BMG_DS018964,Corneal erosion
+BMGC_DS06221,BMG_DS018965,Pulmonary Cystic Fibrosis
+BMGC_DS06222,BMG_DS018970,Mucositis following radiation therapy
+BMGC_DS06223,BMG_DS018974,malignant mesothelioma
+BMGC_DS06224,BMG_DS018975,Benign pemphigus
+BMGC_DS06225,BMG_DS018976,Acrodermatitis continua of Hallopeau
+BMGC_DS06226,BMG_DS018979,Necrobiosis Lipoidica Diabeticorum
+BMGC_DS06227,BMG_DS018987,Anomalous atrioventricular excitation
+BMGC_DS06228,BMG_DS018988,Roberts-SC phocomelia syndrome
+BMGC_DS06229,BMG_DS018989,Asymptomatic periapical periodontitis
+BMGC_DS06230,BMG_DS018990,Hypertrophy of tongue papillae
+BMGC_DS06231,BMG_DS018996,Hereditary hemochromatosis
+BMGC_DS06232,BMG_DS018998,Nephrolithiasis
+BMGC_DS06233,BMG_DS019001,Cauda Equina Syndrome
+BMGC_DS06234,BMG_DS019003,"Hemiplegia, Infantile"
+BMGC_DS06235,BMG_DS019004,Hereditary peripheral neuropathy
+BMGC_DS06236,BMG_DS019009,Severe combined immunodeficiency due to adenosine deaminase deficiency
+BMGC_DS06237,BMG_DS019023,Herpes simplex without mention of complication
+BMGC_DS06238,BMG_DS019024,Measles without mention of complication
+BMGC_DS06239,BMG_DS019028,Angiostrongyliasis
+BMGC_DS06240,BMG_DS019036,extranodal nasal NK/T cell lymphoma
+BMGC_DS06241,BMG_DS019037,ovarian carcinosarcoma
+BMGC_DS06242,BMG_DS019064,Non-infective meningitis
+BMGC_DS06243,BMG_DS019099,Rasmussen Syndrome
+BMGC_DS06244,BMG_DS019118,"Cerebellar Ataxia, Early Onset"
+BMGC_DS06245,BMG_DS019123,"Cerebellar Ataxia, Late Onset"
+BMGC_DS06246,BMG_DS019124,Progressive cerebellar ataxia
+BMGC_DS06247,BMG_DS019135,"Muscular Atrophy, Spinal, Type II"
+BMGC_DS06248,BMG_DS019136,Childhood Progressive Bulbar Palsy
+BMGC_DS06249,BMG_DS019137,Distal Spinal Muscular Atrophy
+BMGC_DS06250,BMG_DS019141,Oculopharyngeal Spinal Muscular Atrophy
+BMGC_DS06251,BMG_DS019142,Bulbospinal Neuronopathy
+BMGC_DS06252,BMG_DS019145,Madras-type motor neurone disease
+BMGC_DS06253,BMG_DS019148,Amyotrophic Lateral Sclerosis With Dementia
+BMGC_DS06254,BMG_DS019150,Complicated hereditary spastic paraplegia
+BMGC_DS06255,BMG_DS019152,Troyer syndrome
+BMGC_DS06256,BMG_DS019153,"Vascular Dementia, Acute Onset"
+BMGC_DS06257,BMG_DS019154,Subcortical Vascular Dementia
+BMGC_DS06258,BMG_DS019160,multiple system atrophy
+BMGC_DS06259,BMG_DS019162,"Huntington Disease, Late Onset"
+BMGC_DS06260,BMG_DS019164,Neuroacanthocytosis
+BMGC_DS06261,BMG_DS019170,Benign Hereditary Chorea
+BMGC_DS06262,BMG_DS019174,paroxysmal dystonia
+BMGC_DS06263,BMG_DS019176,Fahr's syndrome (disorder)
+BMGC_DS06264,BMG_DS019177,Aicardi-Goutieres syndrome
+BMGC_DS06265,BMG_DS019179,Dystonia Disorders
+BMGC_DS06266,BMG_DS019182,Idiopathic familial dystonia
+BMGC_DS06267,BMG_DS019185,Idiopathic non-familial dystonia
+BMGC_DS06268,BMG_DS019196,Familial Tremor
+BMGC_DS06269,BMG_DS019204,Opsoclonus-Myoclonus Syndrome
+BMGC_DS06270,BMG_DS019213,Hashimoto's encephalitis
+BMGC_DS06271,BMG_DS019232,"Multiple Sclerosis, Acute Relapsing"
+BMGC_DS06272,BMG_DS019233,"Multiple Sclerosis, Chronic Progressive"
+BMGC_DS06273,BMG_DS019234,"Multiple Sclerosis, Progressive Relapsing"
+BMGC_DS06274,BMG_DS019235,Extrapontine Myelinolysis
+BMGC_DS06275,BMG_DS019239,"Frontal Epilepsy, Benign, Childhood"
+BMGC_DS06276,BMG_DS019240,"Epilepsy, Benign Psychomotor, Childhood"
+BMGC_DS06277,BMG_DS019243,Childhood Benign Occipital Epilepsy
+BMGC_DS06278,BMG_DS019244,Panayiotopoulos Syndrome
+BMGC_DS06279,BMG_DS019247,Amygdalo-Hippocampal Epilepsy
+BMGC_DS06280,BMG_DS019249,Rhinencephalic Epilepsy
+BMGC_DS06281,BMG_DS019250,"Epilepsy, Lateral Temporal"
+BMGC_DS06282,BMG_DS019251,"Epilepsy, Supplementary Motor"
+BMGC_DS06283,BMG_DS019252,"Epilepsy, Cingulate"
+BMGC_DS06284,BMG_DS019254,"Epilepsy, Opercular"
+BMGC_DS06285,BMG_DS019257,Occipital Lobe Epilepsy
+BMGC_DS06286,BMG_DS019259,"Benign Neonatal Epilepsy, Nonfamilial"
+BMGC_DS06287,BMG_DS019260,"Early Childhood Epilepsy, Myoclonic"
+BMGC_DS06288,BMG_DS019262,Cryptogenic Infantile Spasms
+BMGC_DS06289,BMG_DS019263,Symptomatic Infantile Spasms
+BMGC_DS06290,BMG_DS019266,Myoclonic Astatic Epilepsy
+BMGC_DS06291,BMG_DS019267,Myoclonic Absence Epilepsy
+BMGC_DS06292,BMG_DS019268,Early infantile epileptic encephalopathy with suppression bursts
+BMGC_DS06293,BMG_DS019275,"Reflex Epilepsy, Photosensitive"
+BMGC_DS06294,BMG_DS019279,tactile epilepsy
+BMGC_DS06295,BMG_DS019283,Immersion Related Epilepsy
+BMGC_DS06296,BMG_DS019286,Complex Partial Status Epilepticus
+BMGC_DS06297,BMG_DS019287,Headache Disorders
+BMGC_DS06298,BMG_DS019291,Episodic Cluster Headache
+BMGC_DS06299,BMG_DS019295,Atypical Cluster Headache
+BMGC_DS06300,BMG_DS019306,Delayed Sleep Phase Syndrome
+BMGC_DS06301,BMG_DS019309,Sleep-Related Bruxism
+BMGC_DS06302,BMG_DS019312,isolated congenital anosmia
+BMGC_DS06303,BMG_DS019316,"Trigeminal Neuralgia, Idiopathic"
+BMGC_DS06304,BMG_DS019317,Secondary Trigeminal Neuralgia
+BMGC_DS06305,BMG_DS019322,Miller Fisher Syndrome
+BMGC_DS06306,BMG_DS019327,Hereditary motor and sensory neuropathy with optic atrophy (disorder)
+BMGC_DS06307,BMG_DS019328,"Charcot-Marie-Tooth disease, X-linked, 1"
+BMGC_DS06308,BMG_DS019330,Hereditary liability to pressure palsies
+BMGC_DS06309,BMG_DS019334,"Polyradiculoneuropathy, Chronic Inflammatory Demyelinating"
+BMGC_DS06310,BMG_DS019350,Diabetic Asymmetric Polyneuropathy
+BMGC_DS06311,BMG_DS019362,"Polyneuropathy, Critical Illness"
+BMGC_DS06312,BMG_DS019399,Segmental Autonomic Dysfunction
+BMGC_DS06313,BMG_DS019411,Familial infantile myasthenia
+BMGC_DS06314,BMG_DS019420,Neuromuscular Junction Toxic Disorders
+BMGC_DS06315,BMG_DS019430,Anterior Cerebral Circulation Infarction
+BMGC_DS06316,BMG_DS019457,Multicystic Encephalomalacia
+BMGC_DS06317,BMG_DS019465,"Cerebral Palsy, Dystonic-Rigid"
+BMGC_DS06318,BMG_DS019468,Dysequilibrium syndrome
+BMGC_DS06319,BMG_DS019469,"Cerebral Palsy, Atonic"
+BMGC_DS06320,BMG_DS019474,"Coma, Post-Head Injury"
+BMGC_DS06321,BMG_DS019477,psychogenic polydipsia
+BMGC_DS06322,BMG_DS019493,Malignant otitis externa caused by Pseudomonas aeruginosa
+BMGC_DS06323,BMG_DS019512,Stenosis of external auditory canal
+BMGC_DS06324,BMG_DS019515,Chronic tympanitis
+BMGC_DS06325,BMG_DS019520,Acute mucoid otitis media
+BMGC_DS06326,BMG_DS019521,Acute sanguineous otitis media
+BMGC_DS06327,BMG_DS019552,Recurrent Vestibular Neuritis
+BMGC_DS06328,BMG_DS019558,"Tinnitus, Noise Induced"
+BMGC_DS06329,BMG_DS019607,Chronic adenoiditis
+BMGC_DS06330,BMG_DS019628,Congenital laryngeal abductor palsy
+BMGC_DS06331,BMG_DS019629,Congenital laryngeal adductor palsy
+BMGC_DS06332,BMG_DS019636,laryngeal papillomatosis
+BMGC_DS06333,BMG_DS019642,Trousseau's syndrome
+BMGC_DS06334,BMG_DS019647,lymphatic malformation
+BMGC_DS06335,BMG_DS019649,Lipedema
+BMGC_DS06336,BMG_DS019669,Triose phosphate isomerase deficiency
+BMGC_DS06337,BMG_DS019672,Blood group deletion syndrome
+BMGC_DS06338,BMG_DS019689,Specific granule deficiency
+BMGC_DS06339,BMG_DS019690,Myeloperoxidase Deficiency
+BMGC_DS06340,BMG_DS019708,Hypoplasminogenemia
+BMGC_DS06341,BMG_DS019710,Thrombophilia
+BMGC_DS06342,BMG_DS019711,Protein C Deficiency
+BMGC_DS06343,BMG_DS019712,Heparin cofactor II deficiency (disorder)
+BMGC_DS06344,BMG_DS019719,Thromboxane synthetase deficiency
+BMGC_DS06345,BMG_DS019732,Immune thrombocytopenic purpura
+BMGC_DS06346,BMG_DS019737,Chronic congestive splenomegaly
+BMGC_DS06347,BMG_DS019749,Cerebral sarcoidosis
+BMGC_DS06348,BMG_DS019757,Primary immune deficiency disorder
+BMGC_DS06349,BMG_DS019760,"Hyper-IgM Immunodeficiency Syndrome, Type 1"
+BMGC_DS06350,BMG_DS019761,Hyperimmunoglobulinemia D
+BMGC_DS06351,BMG_DS019763,Selective immunoglobulin E deficiency
+BMGC_DS06352,BMG_DS019764,Selective immunoglobulin D deficiency
+BMGC_DS06353,BMG_DS019778,Secretory Component Deficiency
+BMGC_DS06354,BMG_DS019799,Leukocyte adhesion deficiency type 1
+BMGC_DS06355,BMG_DS019800,"Congenital disorder of glycosylation, type 2C"
+BMGC_DS06356,BMG_DS019801,Tuftsin Deficiency
+BMGC_DS06357,BMG_DS019805,Gluthathione synthetase deficiency
+BMGC_DS06358,BMG_DS019806,Gluthathione peroxidase deficiency
+BMGC_DS06359,BMG_DS019808,Classical complement pathway abnormality
+BMGC_DS06360,BMG_DS019820,Properdin deficiency disease
+BMGC_DS06361,BMG_DS019822,Complement Factor D Deficiency
+BMGC_DS06362,BMG_DS019823,Terminal component deficiency
+BMGC_DS06363,BMG_DS019833,Hereditary C1 esterase inhibitor deficiency - deficient factor
+BMGC_DS06364,BMG_DS019834,Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
+BMGC_DS06365,BMG_DS019835,Complement Factor H Deficiency
+BMGC_DS06366,BMG_DS019840,Carboxypeptidase N Deficiency
+BMGC_DS06367,BMG_DS019846,"Immunodeficiency syndrome, variable"
+BMGC_DS06368,BMG_DS019849,Nijmegen Breakage Syndrome
+BMGC_DS06369,BMG_DS019852,Hypopigmentation-immunodeficiency disease
+BMGC_DS06370,BMG_DS019858,Other diseases of hard tissues of teeth
+BMGC_DS06371,BMG_DS019859,anodontia
+BMGC_DS06372,BMG_DS019864,amelogenesis imperfecta type 1
+BMGC_DS06373,BMG_DS019865,"Amelogenesis Imperfecta, Type IB"
+BMGC_DS06374,BMG_DS019866,amelogenesis imperfecta type 2
+BMGC_DS06375,BMG_DS019867,"Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism"
+BMGC_DS06376,BMG_DS019868,"Amelogenesis Imperfecta, Type III"
+BMGC_DS06377,BMG_DS019870,dentinogenesis imperfecta type 3
+BMGC_DS06378,BMG_DS019871,"Dentin dysplasia, type 1"
+BMGC_DS06379,BMG_DS019879,Tooth surface loss
+BMGC_DS06380,BMG_DS019898,Hereditary gingival fibromatosis
+BMGC_DS06381,BMG_DS019931,autosomal dominant prognathism
+BMGC_DS06382,BMG_DS019957,commissural lip pits
+BMGC_DS06383,BMG_DS019965,"Colitis, Microscopic"
+BMGC_DS06384,BMG_DS019966,"Colitis, Lymphocytic"
+BMGC_DS06385,BMG_DS019967,Neutropenic colitis
+BMGC_DS06386,BMG_DS019972,Ulcer of anus and rectum
+BMGC_DS06387,BMG_DS019991,Postoperative ileus
+BMGC_DS06388,BMG_DS020017,Acute hepatitis C
+BMGC_DS06389,BMG_DS020020,Chronic viral hepatitis B with hepatitis D
+BMGC_DS06390,BMG_DS020022,Vascular disorder of liver
+BMGC_DS06391,BMG_DS020054,"Hyperbilirubinemia, Conjugated, Type III"
+BMGC_DS06392,BMG_DS020056,Non-alcoholic Fatty Liver Disease
+BMGC_DS06393,BMG_DS020112,Chronic diarrhea
+BMGC_DS06394,BMG_DS020150,Steroid-Sensitive Nephrotic Syndrome
+BMGC_DS06395,BMG_DS020151,Steroid-resistant nephrotic syndrome
+BMGC_DS06396,BMG_DS020152,Steroid-Dependent Nephrotic Syndrome
+BMGC_DS06397,BMG_DS020153,Finnish congenital nephrotic syndrome
+BMGC_DS06398,BMG_DS020165,Acute post-streptococcal glomerulonephritis
+BMGC_DS06399,BMG_DS020167,Idiopathic crescentic glomerulonephritis
+BMGC_DS06400,BMG_DS020189,"Renal Failure, Progressive, with Hypertension"
+BMGC_DS06401,BMG_DS020192,Chronic Kidney Insufficiency
+BMGC_DS06402,BMG_DS020202,End stage renal failure on dialysis
+BMGC_DS06403,BMG_DS020205,acute papillary necrosis
+BMGC_DS06404,BMG_DS020247,Acute scleroderma renal crisis
+BMGC_DS06405,BMG_DS020249,Anti-Glomerular Basement Membrane Disease
+BMGC_DS06406,BMG_DS020267,Salcedo syndrome
+BMGC_DS06407,BMG_DS020269,"Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness"
+BMGC_DS06408,BMG_DS020271,Renal dysplasia and retinal aplasia (disorder)
+BMGC_DS06409,BMG_DS020272,"Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness"
+BMGC_DS06410,BMG_DS020273,Ochoa syndrome
+BMGC_DS06411,BMG_DS020275,Glomerulopathy with Giant Fibrillar Deposits
+BMGC_DS06412,BMG_DS020277,Dialysis disequilibrium syndrome
+BMGC_DS06413,BMG_DS020282,Adynamic bone disease
+BMGC_DS06414,BMG_DS020307,Disorder of ureter
+BMGC_DS06415,BMG_DS020323,disorder of neck of urinary bladder
+BMGC_DS06416,BMG_DS020324,Obstruction of urinary bladder outflow
+BMGC_DS06417,BMG_DS020346,Uric acid urolithiasis
+BMGC_DS06418,BMG_DS020347,X-linked recessive nephrolithiasis with renal failure
+BMGC_DS06419,BMG_DS020353,Perforation of uterus caused by intrauterine contraceptive device
+BMGC_DS06420,BMG_DS020385,Oligosynaptic Infertility
+BMGC_DS06421,BMG_DS020386,Congenital impairment of spermatozoa motility
+BMGC_DS06422,BMG_DS020387,"Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa"
+BMGC_DS06423,BMG_DS020388,congenital bilateral aplasia of vas deferens from CFTR mutation
+BMGC_DS06424,BMG_DS020395,Asthenozoospermia
+BMGC_DS06425,BMG_DS020396,Teratozoospermia
+BMGC_DS06426,BMG_DS020397,spermatogenic failure 6
+BMGC_DS06427,BMG_DS020698,Pubertal breast hypertrophy
+BMGC_DS06428,BMG_DS020710,Adrenal cortical hypofunction
+BMGC_DS06429,BMG_DS020803,Cutaneous listeriosis
+BMGC_DS06430,BMG_DS020819,Actinic prurigo
+BMGC_DS06431,BMG_DS020869,Chronic small plaque psoriasis
+BMGC_DS06432,BMG_DS020878,Psoriasis of scalp
+BMGC_DS06433,BMG_DS020924,Erosive oral lichen planus
+BMGC_DS06434,BMG_DS020967,nonsyndromic congenital nail disorder 1
+BMGC_DS06435,BMG_DS020985,Loose Anagen Hair Syndrome
+BMGC_DS06436,BMG_DS021001,Ocular Rosacea
+BMGC_DS06437,BMG_DS021013,Hereditary benign telangiectasia (disorder)
+BMGC_DS06438,BMG_DS021034,Neuropathic ulcer of foot due to diabetes mellitus
+BMGC_DS06439,BMG_DS021044,Morbilliform Drug Reaction
+BMGC_DS06440,BMG_DS021059,Poikiloderma of Kindler
+BMGC_DS06441,BMG_DS021061,Pseudoatrophoderma Colli
+BMGC_DS06442,BMG_DS021074,Lethal tight skin contracture syndrome (disorder)
+BMGC_DS06443,BMG_DS021075,Wiedemann-Rautenstrauch syndrome
+BMGC_DS06444,BMG_DS021076,Wrinkly skin syndrome
+BMGC_DS06445,BMG_DS021091,pelvic lipomatosis
+BMGC_DS06446,BMG_DS021093,encephalocraniocutaneous lipomatosis
+BMGC_DS06447,BMG_DS021114,Erythema multiforme-like lupus erythematosus
+BMGC_DS06448,BMG_DS021145,Bullous pyoderma gangrenosum
+BMGC_DS06449,BMG_DS021156,autosomal recessive hypohidrotic ectodermal dysplasia
+BMGC_DS06450,BMG_DS021157,Rudiger syndrome 1
+BMGC_DS06451,BMG_DS021158,Basan syndrome
+BMGC_DS06452,BMG_DS021159,Hay-Wells syndrome
+BMGC_DS06453,BMG_DS021161,Fried's tooth and nail syndrome
+BMGC_DS06454,BMG_DS021162,wooly hair-hypotrichosis-everted lower lip-outstanding ears syndrome
+BMGC_DS06455,BMG_DS021164,"Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy"
+BMGC_DS06456,BMG_DS021165,Trichodental syndrome
+BMGC_DS06457,BMG_DS021166,Orofaciodigital syndrome 3
+BMGC_DS06458,BMG_DS021167,Orofaciodigital syndrome 4
+BMGC_DS06459,BMG_DS021170,Curly hair-ankyloblepharon-nail dysplasia syndrome
+BMGC_DS06460,BMG_DS021172,Hypoplastic enamel-onycholysis-hypohidrosis syndrome
+BMGC_DS06461,BMG_DS021176,Kohlschutter Tonz syndrome
+BMGC_DS06462,BMG_DS021183,Keratolytic winter erythema
+BMGC_DS06463,BMG_DS021184,hereditary palmoplantar keratoderma
+BMGC_DS06464,BMG_DS021185,Congenital palmoplantar and perioral keratoderma of Olmsted
+BMGC_DS06465,BMG_DS021189,palmoplantar keratoderma-sclerodactyly syndrome
+BMGC_DS06466,BMG_DS021193,dyschromatosis symmetrica hereditaria
+BMGC_DS06467,BMG_DS021195,dermatopathia pigmentosa reticularis
+BMGC_DS06468,BMG_DS021210,syringocystadenoma papilliferum
+BMGC_DS06469,BMG_DS021213,Carney Complex
+BMGC_DS06470,BMG_DS021214,Reticulate acropigmentation of Kitamura
+BMGC_DS06471,BMG_DS021215,familial cutaneous collagenoma
+BMGC_DS06472,BMG_DS021216,congenital smooth muscle hamartoma
+BMGC_DS06473,BMG_DS021275,Protrusio acetabuli
+BMGC_DS06474,BMG_DS021401,juvenile chronic polyarthritis
+BMGC_DS06475,BMG_DS021407,Juvenile ankylosing spondylitis
+BMGC_DS06476,BMG_DS021499,"Chronic Infantile Neurological, Cutaneous, and Articular Syndrome"
+BMGC_DS06477,BMG_DS021602,"Osteoarthritis, Knee"
+BMGC_DS06478,BMG_DS021614,lupus erythematosus
+BMGC_DS06479,BMG_DS021639,Nodular fasciitis
+BMGC_DS06480,BMG_DS021661,trigger thumb
+BMGC_DS06481,BMG_DS021665,"Dupuytren's disease of finger, with contracture"
+BMGC_DS06482,BMG_DS021732,Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)
+BMGC_DS06483,BMG_DS021733,Fukuyama Type Congenital Muscular Dystrophy
+BMGC_DS06484,BMG_DS021738,Ullrich congenital muscular dystrophy 1
+BMGC_DS06485,BMG_DS021739,Eichsfeld type congenital muscular dystrophy
+BMGC_DS06486,BMG_DS021746,"Muscular Dystrophy, Emery-Dreifuss"
+BMGC_DS06487,BMG_DS021747,"Emery-Dreifuss muscular dystrophy 2, autosomal dominant"
+BMGC_DS06488,BMG_DS021749,"Muscular Dystrophy, Scapulohumeral"
+BMGC_DS06489,BMG_DS021759,X-linked myotubular myopathy
+BMGC_DS06490,BMG_DS021760,"Myopathy, Centronuclear, Autosomal Recessive"
+BMGC_DS06491,BMG_DS021763,Tubular Aggregate Myopathy
+BMGC_DS06492,BMG_DS021768,Myopathy with Abnormal Lipid Metabolism
+BMGC_DS06493,BMG_DS021777,Congenital Myotonic Dystrophy
+BMGC_DS06494,BMG_DS021879,Chronic multifocal osteomyelitis
+BMGC_DS06495,BMG_DS021943,Skeletal dysplasia
+BMGC_DS06496,BMG_DS021944,Hypochondroplasia (disorder)
+BMGC_DS06497,BMG_DS021945,Metachondromatosis
+BMGC_DS06498,BMG_DS021949,pseudoachondroplasia
+BMGC_DS06499,BMG_DS021950,Craniodiaphyseal dysplasia
+BMGC_DS06500,BMG_DS021974,Synovial Hypertrophy
+BMGC_DS06501,BMG_DS021994,cervical disk degenerative disorder
+BMGC_DS06502,BMG_DS022238,"Seizures, Somatosensory"
+BMGC_DS06503,BMG_DS022244,Lazy Eye
+BMGC_DS06504,BMG_DS022254,Superior Oblique Myokymia
+BMGC_DS06505,BMG_DS022255,telecanthus
+BMGC_DS06506,BMG_DS022261,enophthalmos
+BMGC_DS06507,BMG_DS022264,heterochromia iridis
+BMGC_DS06508,BMG_DS022271,retinal arterial tortuosity
+BMGC_DS06509,BMG_DS022274,"Low Back Pain, Mechanical"
+BMGC_DS06510,BMG_DS022280,"Neuralgia, Perineal"
+BMGC_DS06511,BMG_DS022281,"Neuralgia, Iliohypogastric Nerve"
+BMGC_DS06512,BMG_DS022284,Scurfiness of scalp
+BMGC_DS06513,BMG_DS022307,Spastic Quadriplegia
+BMGC_DS06514,BMG_DS022309,Facial Paresis
+BMGC_DS06515,BMG_DS022321,Aortic valve calcification
+BMGC_DS06516,BMG_DS022328,Dilatation of pulmonary artery (disorder)
+BMGC_DS06517,BMG_DS022329,sinoatrial node disorder
+BMGC_DS06518,BMG_DS022331,Supraventricular arrhythmia
+BMGC_DS06519,BMG_DS022348,anaplastic oligoastrocytoma
+BMGC_DS06520,BMG_DS022349,choroid plexus carcinoma
+BMGC_DS06521,BMG_DS022352,choroid plexus meningioma
+BMGC_DS06522,BMG_DS022353,lymphoplasmacyte-rich meningioma
+BMGC_DS06523,BMG_DS022354,clear cell meningioma
+BMGC_DS06524,BMG_DS022355,cellular schwannoma
+BMGC_DS06525,BMG_DS022356,papillary craniopharyngioma
+BMGC_DS06526,BMG_DS022357,adamantinous craniopharyngioma
+BMGC_DS06527,BMG_DS022367,aprosencephaly
+BMGC_DS06528,BMG_DS022371,lobar holoprosencephaly
+BMGC_DS06529,BMG_DS022372,alobar holoprosencephaly
+BMGC_DS06530,BMG_DS022375,Classical Lissencephaly
+BMGC_DS06531,BMG_DS022377,cerebral cortical dysplasia
+BMGC_DS06532,BMG_DS022379,colpocephaly
+BMGC_DS06533,BMG_DS022380,Hemimegalencephaly
+BMGC_DS06534,BMG_DS022381,Familial aplasia of the vermis
+BMGC_DS06535,BMG_DS022383,Gillespie syndrome
+BMGC_DS06536,BMG_DS022384,Asymmetric crying face association
+BMGC_DS06537,BMG_DS022386,Vein of Galen aneurysm
+BMGC_DS06538,BMG_DS022395,Mayer-Rokitansky-Kuster syndrome
+BMGC_DS06539,BMG_DS022397,"renal hypoplasia, bilateral"
+BMGC_DS06540,BMG_DS022398,Renal cysts and diabetes syndrome
+BMGC_DS06541,BMG_DS022400,"renal dysplasia, unilateral"
+BMGC_DS06542,BMG_DS022401,"renal dysplasia, bilateral"
+BMGC_DS06543,BMG_DS022407,Multiple renal cysts
+BMGC_DS06544,BMG_DS022418,"thumbs, congenital Clasped"
+BMGC_DS06545,BMG_DS022420,postaxial polydactyly of fingers
+BMGC_DS06546,BMG_DS022424,split foot
+BMGC_DS06547,BMG_DS022429,cleft hard palate
+BMGC_DS06548,BMG_DS022430,cleft soft palate
+BMGC_DS06549,BMG_DS022434,trigonocephaly 1
+BMGC_DS06550,BMG_DS022435,Kleeblattschaedel syndrome
+BMGC_DS06551,BMG_DS022436,"cervical vertebrae, agenesis of"
+BMGC_DS06552,BMG_DS022443,Schneckenbecken dysplasia
+BMGC_DS06553,BMG_DS022444,short rib dysplasia
+BMGC_DS06554,BMG_DS022445,"Short rib-polydactyly syndrome, Verma-Naumoff type"
+BMGC_DS06555,BMG_DS022446,"Short rib-polydactyly syndrome, Beemer type"
+BMGC_DS06556,BMG_DS022447,Boomerang dysplasia
+BMGC_DS06557,BMG_DS022448,Pseudodiastrophic dysplasia
+BMGC_DS06558,BMG_DS022450,"Dyssegmental dysplasia, Rolland-Desbuquois type"
+BMGC_DS06559,BMG_DS022451,Spondyloepimetaphyseal disorder
+BMGC_DS06560,BMG_DS022452,"Spondyloepimetaphyseal Dysplasia, Irapa Type"
+BMGC_DS06561,BMG_DS022453,Namaqualand hip dysplasia
+BMGC_DS06562,BMG_DS022454,Progressive pseudorheumatoid dysplasia
+BMGC_DS06563,BMG_DS022455,Wolcott-Rallison syndrome
+BMGC_DS06564,BMG_DS022457,Opsismodysplasia
+BMGC_DS06565,BMG_DS022458,"Spondylometaphyseal dysplasia, 'corner fracture' type"
+BMGC_DS06566,BMG_DS022459,Spondyloenchondrodysplasia
+BMGC_DS06567,BMG_DS022460,"chondrodysplasia punctata, tibial-metacarpal type"
+BMGC_DS06568,BMG_DS022461,Metaphyseal chondrodysplasia Spahr type
+BMGC_DS06569,BMG_DS022462,Metaphyseal anadysplasia
+BMGC_DS06570,BMG_DS022463,autosomal dominant brachyolmia
+BMGC_DS06571,BMG_DS022464,Brachyolmia
+BMGC_DS06572,BMG_DS022466,Langer mesomelic dysplasia
+BMGC_DS06573,BMG_DS022467,Nievergelt syndrome
+BMGC_DS06574,BMG_DS022468,Trichorhinophalangeal dysplasia type I
+BMGC_DS06575,BMG_DS022469,CRANIOECTODERMAL DYSPLASIA 1
+BMGC_DS06576,BMG_DS022470,bent bone dysplasia
+BMGC_DS06577,BMG_DS022471,Kyphomelic dysplasia
+BMGC_DS06578,BMG_DS022472,Desbuquois syndrome
+BMGC_DS06579,BMG_DS022473,Spondyloepimetaphyseal Dysplasia With Joint Laxity
+BMGC_DS06580,BMG_DS022475,"Microcephalic Osteodysplastic Primordial Dwarfism, Type II"
+BMGC_DS06581,BMG_DS022476,Osteoporosis with pseudoglioma
+BMGC_DS06582,BMG_DS022477,Bruck syndrome
+BMGC_DS06583,BMG_DS022478,Singleton Merten syndrome
+BMGC_DS06584,BMG_DS022479,Geroderma osteodysplastica
+BMGC_DS06585,BMG_DS022483,Osteopetrosis - intermediate type
+BMGC_DS06586,BMG_DS022484,Dysosteosclerosis
+BMGC_DS06587,BMG_DS022486,Axial osteosclerosis
+BMGC_DS06588,BMG_DS022487,IBIDS Syndrome
+BMGC_DS06589,BMG_DS022488,Osteopathia striata cranial sclerosis
+BMGC_DS06590,BMG_DS022489,Lenz-Majewski hyperostotic dwarfism
+BMGC_DS06591,BMG_DS022491,Van Buchem disease
+BMGC_DS06592,BMG_DS022492,Worth disease
+BMGC_DS06593,BMG_DS022495,Dysplasia epiphysealis hemimelica
+BMGC_DS06594,BMG_DS022496,osteoglophonic dwarfism
+BMGC_DS06595,BMG_DS022497,infantile myofibromatosis
+BMGC_DS06596,BMG_DS022499,Dermochondrocorneal dystrophy of François
+BMGC_DS06597,BMG_DS022500,Winchester syndrome (disorder)
+BMGC_DS06598,BMG_DS022501,Mandibuloacral dysostosis
+BMGC_DS06599,BMG_DS022502,familial expansile osteolysis
+BMGC_DS06600,BMG_DS022504,autosomal dominant ichthyosis vulgaris
+BMGC_DS06601,BMG_DS022506,"Lamellar ichthyosis, autosomal dominant form"
+BMGC_DS06602,BMG_DS022507,superficial epidermolytic ichthyosis
+BMGC_DS06603,BMG_DS022509,"ichthyosis histrix, Lambert type"
+BMGC_DS06604,BMG_DS022512,"epidermolysis bullosa simplex 2F, with mottled pigmentation"
+BMGC_DS06605,BMG_DS022513,"Epidermolysis bullosa simplex, Ogna type"
+BMGC_DS06606,BMG_DS022515,pretibial dystrophic epidermolysis bullosa
+BMGC_DS06607,BMG_DS022516,generalized dominant dystrophic epidermolysis bullosa
+BMGC_DS06608,BMG_DS022518,Junctional epidermolysis bullosa mitis
+BMGC_DS06609,BMG_DS022522,Cutis Laxa-Marfanoid Syndrome
+BMGC_DS06610,BMG_DS022523,autosomal recessive cutis laxa type I
+BMGC_DS06611,BMG_DS022528,Uncombable hair syndrome
+BMGC_DS06612,BMG_DS022530,isolated congenital breast hypoplasia/aplasia
+BMGC_DS06613,BMG_DS022531,Isotretinoin embryopathy like syndrome
+BMGC_DS06614,BMG_DS022551,"Down Syndrome, Partial Trisomy 21"
+BMGC_DS06615,BMG_DS022552,"Trisomy 21, Meiotic Nondisjunction"
+BMGC_DS06616,BMG_DS022568,Chromosome 18p deletion syndrome
+BMGC_DS06617,BMG_DS022569,Deletion of long arm of chromosome 18
+BMGC_DS06618,BMG_DS022593,post-transplant lymphoproliferative disease
+BMGC_DS06619,BMG_DS022594,lower lip cancer
+BMGC_DS06620,BMG_DS022596,Proliferative fasciitis
+BMGC_DS06621,BMG_DS022597,Intravascular fasciitis
+BMGC_DS06622,BMG_DS022598,upper lip cancer
+BMGC_DS06623,BMG_DS022599,lower gum cancer
+BMGC_DS06624,BMG_DS022629,Non-specific granulomatous orchitis
+BMGC_DS06625,BMG_DS022631,Myoclonic Encephalopathy
+BMGC_DS06626,BMG_DS022646,substance dependence
+BMGC_DS06627,BMG_DS022651,Neuropathy
+BMGC_DS06628,BMG_DS022658,Urolithiasis
+BMGC_DS06629,BMG_DS022664,Neuropathy in association with hereditary ataxia
+BMGC_DS06630,BMG_DS022674,Posterior Cerebral Artery Syndrome
+BMGC_DS06631,BMG_DS022686,Immunodeficiency following hereditary defective response to Epstein-Barr virus
+BMGC_DS06632,BMG_DS022704,"Nephrotic syndrome, focal and segmental glomerular lesions"
+BMGC_DS06633,BMG_DS022818,"Conductive hearing loss, bilateral"
+BMGC_DS06634,BMG_DS022820,Sensorineural hearing loss of bilateral ears
+BMGC_DS06635,BMG_DS022856,stuttering
+BMGC_DS06636,BMG_DS022882,Oral Dyskinesia
+BMGC_DS06637,BMG_DS022901,Expressive language delay
+BMGC_DS06638,BMG_DS022905,Benedict Syndrome
+BMGC_DS06639,BMG_DS022906,Foville Syndrome
+BMGC_DS06640,BMG_DS022907,Weber Syndrome
+BMGC_DS06641,BMG_DS022908,Top of the Basilar Syndrome
+BMGC_DS06642,BMG_DS022918,"Hydrops Fetalis, Non-Immune"
+BMGC_DS06643,BMG_DS022919,Immune Hydrops Fetalis
+BMGC_DS06644,BMG_DS022974,Sepsis of the newborn
+BMGC_DS06645,BMG_DS022977,Neonatal meningitis
+BMGC_DS06646,BMG_DS022991,Osteopenia of prematurity
+BMGC_DS06647,BMG_DS022996,Simple Endometrial Hyperplasia
+BMGC_DS06648,BMG_DS022997,Peutz-Jeghers polyp
+BMGC_DS06649,BMG_DS023001,"Median Neuropathy, Proximal"
+BMGC_DS06650,BMG_DS023015,non-secretory myeloma
+BMGC_DS06651,BMG_DS023017,enteropathy-associated T-cell lymphoma
+BMGC_DS06652,BMG_DS023018,familial primary pulmonary hypoplasia
+BMGC_DS06653,BMG_DS023019,Blindness
+BMGC_DS06654,BMG_DS023027,Weyers acrofacial dysostosis
+BMGC_DS06655,BMG_DS023030,Muscle eye brain disease
+BMGC_DS06656,BMG_DS023060,Complex Regional Pain Syndromes
+BMGC_DS06657,BMG_DS023108,Generalized myasthenia
+BMGC_DS06658,BMG_DS023109,Hemorrhagic cerebral infarction
+BMGC_DS06659,BMG_DS023112,Posterior Circulation Transient Ischemic Attack
+BMGC_DS06660,BMG_DS023127,cavernous hemangiomas of face-supraumbilical midline raphe syndrome
+BMGC_DS06661,BMG_DS023138,Anemia of renal disease
+BMGC_DS06662,BMG_DS023171,Alpha trait thalassemia
+BMGC_DS06663,BMG_DS023175,Beta thalassemia intermedia
+BMGC_DS06664,BMG_DS023181,Hemoglobin E/beta thalassemia disease
+BMGC_DS06665,BMG_DS023193,Hemolytic anemia due to hexokinase deficiency
+BMGC_DS06666,BMG_DS023202,Hypodysfibrinogenemia
+BMGC_DS06667,BMG_DS023209,X-linked agammaglobulinemia with growth hormone deficiency
+BMGC_DS06668,BMG_DS023212,WHIM syndrome
+BMGC_DS06669,BMG_DS023236,Renal hypouricemia
+BMGC_DS06670,BMG_DS023298,Hypoalphalipoproteinemias
+BMGC_DS06671,BMG_DS023307,Vibratory angioedema
+BMGC_DS06672,BMG_DS023322,Achenbach syndrome
+BMGC_DS06673,BMG_DS023328,porokeratotic eccrine ostial and dermal duct nevus
+BMGC_DS06674,BMG_DS023330,Michelin tire baby syndrome
+BMGC_DS06675,BMG_DS023406,Nerve fiber bundle defect
+BMGC_DS06676,BMG_DS023411,Optic Disc Neovascularization
+BMGC_DS06677,BMG_DS023418,Corneal edema caused by wearing of contact lenses
+BMGC_DS06678,BMG_DS023421,endometrioid tumor
+BMGC_DS06679,BMG_DS023427,malignant melanocytic neoplasm of the peripheral nerve sheath
+BMGC_DS06680,BMG_DS023429,upper lip cancer
+BMGC_DS06681,BMG_DS023430,tongue cancer
+BMGC_DS06682,BMG_DS023433,dermal unilateral segmental cavernous angioma
+BMGC_DS06683,BMG_DS023495,Disorder of keratinization
+BMGC_DS06684,BMG_DS023496,Alpha thalassaemia-mental retardation syndrome
+BMGC_DS06685,BMG_DS023498,endometrial carcinoma
+BMGC_DS06686,BMG_DS023499,ovarian papillary tumor
+BMGC_DS06687,BMG_DS023501,hemangiopericytic tumor
+BMGC_DS06688,BMG_DS023503,synovium neoplasm
+BMGC_DS06689,BMG_DS023504,dyslexia
+BMGC_DS06690,BMG_DS023505,breath-holding Spells
+BMGC_DS06691,BMG_DS023521,Other specified coagulation defects
+BMGC_DS06692,BMG_DS023522,Other primary thrombocytopenia
+BMGC_DS06693,BMG_DS023523,Other specified disorders of white blood cells
+BMGC_DS06694,BMG_DS023528,Other combined immunodeficiencies
+BMGC_DS06695,BMG_DS023545,extrapyramidal and movement disease
+BMGC_DS06696,BMG_DS023549,Other dystonia
+BMGC_DS06697,BMG_DS023550,Other specified extrapyramidal and movement disorders
+BMGC_DS06698,BMG_DS023552,Other specified degenerative diseases of nervous system
+BMGC_DS06699,BMG_DS023558,Other forms of migraine
+BMGC_DS06700,BMG_DS023566,Other hereditary and idiopathic neuropathies
+BMGC_DS06701,BMG_DS023591,Post-Traumatic Hydrocephalus
+BMGC_DS06702,BMG_DS023656,Other chondrocalcinosis
+BMGC_DS06703,BMG_DS023744,Other chronic tubulo-interstitial nephritis
+BMGC_DS06704,BMG_DS023761,Other specified urinary incontinence
+BMGC_DS06705,BMG_DS023815,Other congenital ichthyosis
+BMGC_DS06706,BMG_DS023817,Other congenital malformation syndromes with other skeletal changes
+BMGC_DS06707,BMG_DS023831,rheumatic myocarditis
+BMGC_DS06708,BMG_DS023834,Low compliance bladder
+BMGC_DS06709,BMG_DS023844,Infection due to Brucella canis
+BMGC_DS06710,BMG_DS023889,kidney cancer
+BMGC_DS06711,BMG_DS023892,Other nutritional anemias
+BMGC_DS06712,BMG_DS023899,Other hereditary hemolytic anemias
+BMGC_DS06713,BMG_DS023910,Other specified immunodeficiencies
+BMGC_DS06714,BMG_DS023913,Other hypothyroidism
+BMGC_DS06715,BMG_DS023919,Hyperparathyroidism and other disorders of parathyroid gland
+BMGC_DS06716,BMG_DS023921,Hypofunction and other disorders of the pituitary gland
+BMGC_DS06717,BMG_DS023923,Other disorders of adrenal gland
+BMGC_DS06718,BMG_DS023929,Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
+BMGC_DS06719,BMG_DS023930,Other disorders of amino-acid metabolism
+BMGC_DS06720,BMG_DS023931,Other disorders of carbohydrate metabolism
+BMGC_DS06721,BMG_DS023932,Disorders of sphingolipid metabolism and other lipid storage disorders
+BMGC_DS06722,BMG_DS023934,Disorders of porphyrin and bilirubin metabolism
+BMGC_DS06723,BMG_DS023939,"Lipodystrophy, not elsewhere classified"
+BMGC_DS06724,BMG_DS023950,Spinal muscular atrophy and related syndromes
+BMGC_DS06725,BMG_DS023954,"Alzheimer Disease, Late Onset"
+BMGC_DS06726,BMG_DS023955,"Other degenerative diseases of nervous system, not elsewhere classified"
+BMGC_DS06727,BMG_DS023965,Mononeuropathies
+BMGC_DS06728,BMG_DS023971,Other disorders of brain
+BMGC_DS06729,BMG_DS023987,inner ear disorder
+BMGC_DS06730,BMG_DS023988,"Other disorders of ear, not elsewhere classified"
+BMGC_DS06731,BMG_DS023995,Other pulmonary heart diseases
+BMGC_DS06732,BMG_DS024047,"Noninfective gastroenteritis and colitis, unspecified"
+BMGC_DS06733,BMG_DS024076,Other nonscarring hair loss
+BMGC_DS06734,BMG_DS024078,Other follicular disorders
+BMGC_DS06735,BMG_DS024085,Other rheumatoid arthritis
+BMGC_DS06736,BMG_DS024086,Other arthritis
+BMGC_DS06737,BMG_DS024090,"Other joint disorder, not elsewhere classified"
+BMGC_DS06738,BMG_DS024108,Other disorders of bone density and structure
+BMGC_DS06739,BMG_DS024109,Other disorders of bone
+BMGC_DS06740,BMG_DS024140,hernia of ovary and fallopian tube
+BMGC_DS06741,BMG_DS024172,Noninfective neonatal diarrhea
+BMGC_DS06742,BMG_DS024179,neurofibromatosis
+BMGC_DS06743,BMG_DS024180,Other specified congenital malformation syndromes affecting multiple systems
+BMGC_DS06744,BMG_DS024181,Congenital malformation syndromes involving early overgrowth
+BMGC_DS06745,BMG_DS024184,tongue cancer
+BMGC_DS06746,BMG_DS024185,oral cavity cancer
+BMGC_DS06747,BMG_DS024187,epiglottis cancer
+BMGC_DS06748,BMG_DS024188,postcricoid region cancer
+BMGC_DS06749,BMG_DS024189,hypopharynx cancer
+BMGC_DS06750,BMG_DS024191,malignant neoplasm of abdominal esophagus
+BMGC_DS06751,BMG_DS024192,appendix cancer
+BMGC_DS06752,BMG_DS024193,islet cell tumor
+BMGC_DS06753,BMG_DS024195,labium majus cancer
+BMGC_DS06754,BMG_DS024196,labia minora cancer
+BMGC_DS06755,BMG_DS024197,bladder trigone cancer
+BMGC_DS06756,BMG_DS024198,bladder dome cancer
+BMGC_DS06757,BMG_DS024199,bladder lateral wall cancer
+BMGC_DS06758,BMG_DS024200,ciliary body cancer
+BMGC_DS06759,BMG_DS024202,malignant olfactory nerve neoplasm
+BMGC_DS06760,BMG_DS024203,pituitary cancer
+BMGC_DS06761,BMG_DS024204,liver carcinoma in situ
+BMGC_DS06762,BMG_DS024216,Lymphadenopathy
+BMGC_DS06763,BMG_DS024218,cardiovascular neoplasm
+BMGC_DS06764,BMG_DS024220,dementia
+BMGC_DS06765,BMG_DS024224,congenital nervous system disorder
+BMGC_DS06766,BMG_DS024229,Pneumonia due to Klebsiella pneumoniae
+BMGC_DS06767,BMG_DS024231,colon lymphoma
+BMGC_DS06768,BMG_DS024234,lung lymphoma
+BMGC_DS06769,BMG_DS024238,Necrotizing Enterocolitis
+BMGC_DS06770,BMG_DS024241,somatization disorder
+BMGC_DS06771,BMG_DS024261,Fibrosis of bile duct
+BMGC_DS06772,BMG_DS024264,Acute pyelonephritis
+BMGC_DS06773,BMG_DS024266,Urethral atrophy
+BMGC_DS06774,BMG_DS024274,"Sleep Apnea, Obstructive"
+BMGC_DS06775,BMG_DS024275,"Sleep Apnea, Central"
+BMGC_DS06776,BMG_DS024283,Opticocochleodentate Degeneration
+BMGC_DS06777,BMG_DS024286,Pallidopontonigral degeneration
+BMGC_DS06778,BMG_DS024288,Spinopontine Atrophy
+BMGC_DS06779,BMG_DS024293,Retraction Nystagmus
+BMGC_DS06780,BMG_DS024298,Hereditary pyropoikilocytosis
+BMGC_DS06781,BMG_DS024307,Staphylococcal endocarditis
+BMGC_DS06782,BMG_DS024313,Klebsiella cystitis
+BMGC_DS06783,BMG_DS024314,Chlamydial pelvic inflammatory disease
+BMGC_DS06784,BMG_DS024361,Brain Stem Infarctions
+BMGC_DS06785,BMG_DS024365,coloboma of eyelid
+BMGC_DS06786,BMG_DS024377,Peritoneal Fibrosis
+BMGC_DS06787,BMG_DS024379,Emphysematous Cholecystitis
+BMGC_DS06788,BMG_DS024393,Neonatal respiratory failure
+BMGC_DS06789,BMG_DS024397,"Motor Neuron Disease, Upper"
+BMGC_DS06790,BMG_DS024398,Acute Confusional Migraine
+BMGC_DS06791,BMG_DS024401,Primary Thunderclap Headache
+BMGC_DS06792,BMG_DS024422,Atrophic retina
+BMGC_DS06793,BMG_DS024429,Bilateral cataracts (disorder)
+BMGC_DS06794,BMG_DS024440,"Corneal dystrophy, epithelial basement membrane"
+BMGC_DS06795,BMG_DS024448,Lower eyelid ectropion
+BMGC_DS06796,BMG_DS024460,Temporary Nystagmus
+BMGC_DS06797,BMG_DS024461,Permanent Nystagmus
+BMGC_DS06798,BMG_DS024462,Unidirectional Nystagmus
+BMGC_DS06799,BMG_DS024463,Multidirectional Nystagmus
+BMGC_DS06800,BMG_DS024464,Conjugate Nystagmus
+BMGC_DS06801,BMG_DS024465,Convergence Nystagmus
+BMGC_DS06802,BMG_DS024466,Fatigable Positional Nystagmus
+BMGC_DS06803,BMG_DS024467,Non-Fatigable Positional Nystagmus
+BMGC_DS06804,BMG_DS024482,Congenital atransferrinemia
+BMGC_DS06805,BMG_DS024514,Primary Exertional Headache
+BMGC_DS06806,BMG_DS024522,subcutaneous panniculitis-like T-cell lymphoma
+BMGC_DS06807,BMG_DS024523,acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22)
+BMGC_DS06808,BMG_DS024524,acute myeloid leukemia with minimal differentiation
+BMGC_DS06809,BMG_DS024526,Pseudoaphakia
+BMGC_DS06810,BMG_DS024527,pervasive developmental disorder
+BMGC_DS06811,BMG_DS024529,Mulibrey Nanism
+BMGC_DS06812,BMG_DS024530,Chronic Alcoholic Hepatitis
+BMGC_DS06813,BMG_DS024531,Cryptogenic Chronic Hepatitis
+BMGC_DS06814,BMG_DS024532,Metabolic Syndrome X
+BMGC_DS06815,BMG_DS024533,Lymphatism
+BMGC_DS06816,BMG_DS024534,Status Lymphaticus
+BMGC_DS06817,BMG_DS024535,opiate dependence
+BMGC_DS06818,BMG_DS024536,Neuropapillitis
+BMGC_DS06819,BMG_DS024537,"Periodontitis, Acute Nonsuppurative"
+BMGC_DS06820,BMG_DS024538,Meningeal Plague
+BMGC_DS06821,BMG_DS024539,Pneumonic Plague
+BMGC_DS06822,BMG_DS024540,Pulmonary Thromboembolisms
+BMGC_DS06823,BMG_DS024545,"Lung, Hyperlucent"
+BMGC_DS06824,BMG_DS024546,retina neoplasm
+BMGC_DS06825,BMG_DS024547,optic nerve neoplasm
+BMGC_DS06826,BMG_DS024548,Intracranial Hypotension
+BMGC_DS06827,BMG_DS024549,Neurodegenerative Disorders
+BMGC_DS06828,BMG_DS024550,"Hepatitis B, Chronic"
+BMGC_DS06829,BMG_DS024551,"Hepatitis C, Chronic"
+BMGC_DS06830,BMG_DS024553,"Hepatitis, Chronic, Drug-Induced"
+BMGC_DS06831,BMG_DS024554,Schnitzler Syndrome
+BMGC_DS06832,BMG_DS024555,mood disorder
+BMGC_DS06833,BMG_DS024558,Stress polycythemia
+BMGC_DS06834,BMG_DS024559,atrial standstill
+BMGC_DS06835,BMG_DS024560,muscular atrophy
+BMGC_DS06836,BMG_DS024561,carcinoma of duodenum
+BMGC_DS06837,BMG_DS024565,Non-Q wave myocardial infarction
+BMGC_DS06838,BMG_DS024573,hypochondrogenesis
+BMGC_DS06839,BMG_DS024575,renal agenesis
+BMGC_DS06840,BMG_DS024576,cerebral meningioma
+BMGC_DS06841,BMG_DS024577,Glycogen Storage Disease IXB
+BMGC_DS06842,BMG_DS024579,Glycinuria with or without Oxalate Urolithiasis
+BMGC_DS06843,BMG_DS024591,Idiopathic Autoimmune Hemolytic Anemia
+BMGC_DS06844,BMG_DS024596,"Neutrophilia, Hereditary"
+BMGC_DS06845,BMG_DS024600,"Klinefelter Syndrome, Variants"
+BMGC_DS06846,BMG_DS024602,Idiopathic hypercalciuria
+BMGC_DS06847,BMG_DS024607,Atherosclerotic occlusive disease
+BMGC_DS06848,BMG_DS024609,"Motor Neuron Disease, Secondary"
+BMGC_DS06849,BMG_DS024610,"Amyotrophic Lateral Sclerosis, Guam Form"
+BMGC_DS06850,BMG_DS024611,"Apraxia, oculomotor, Cogan type"
+BMGC_DS06851,BMG_DS024613,Epileptic encephalopathy
+BMGC_DS06852,BMG_DS024614,schizophrenia 10
+BMGC_DS06853,BMG_DS024615,Chandler syndrome
+BMGC_DS06854,BMG_DS024618,Elephantiasis Nostras Verrucosa
+BMGC_DS06855,BMG_DS024621,"Myositis, Proliferative"
+BMGC_DS06856,BMG_DS024629,nonsyndromic congenital nail disorder 3
+BMGC_DS06857,BMG_DS024630,neurocutaneous melanocytosis
+BMGC_DS06858,BMG_DS024633,Acrokeratoelastoidosis of Costa
+BMGC_DS06859,BMG_DS024634,myxoid/round cell liposarcoma
+BMGC_DS06860,BMG_DS024635,composite lymphoma
+BMGC_DS06861,BMG_DS024638,"Nemaline Myopathy, Childhood Onset"
+BMGC_DS06862,BMG_DS024640,Congenital Fiber Type Disproportion
+BMGC_DS06863,BMG_DS024643,Exudative glomerulonephritis
+BMGC_DS06864,BMG_DS024651,multiple self-healing squamous epithelioma
+BMGC_DS06865,BMG_DS024653,Dermatophytosis of the body
+BMGC_DS06866,BMG_DS024654,intrahepatic bile duct cancer
+BMGC_DS06867,BMG_DS024655,esophageal cancer
+BMGC_DS06868,BMG_DS024656,Nodding spasm
+BMGC_DS06869,BMG_DS024664,monilethrix
+BMGC_DS06870,BMG_DS024665,"preauricular fistulae, congenital"
+BMGC_DS06871,BMG_DS024673,Cutaneous schistosomiasis
+BMGC_DS06872,BMG_DS024674,"Larva Migrans, Cutaneous"
+BMGC_DS06873,BMG_DS024676,oligoastrocytoma
+BMGC_DS06874,BMG_DS024687,Pseudofolliculitis barbae (disorder)
+BMGC_DS06875,BMG_DS024689,North Asian Tick Typhus
+BMGC_DS06876,BMG_DS024698,Meibomianitis
+BMGC_DS06877,BMG_DS024700,Obstructive Hydrocephalus
+BMGC_DS06878,BMG_DS024701,X-linked lymphoproliferative syndrome
+BMGC_DS06879,BMG_DS024703,Preglaucoma
+BMGC_DS06880,BMG_DS024704,malignant superior sulcus neoplasm
+BMGC_DS06881,BMG_DS024706,thyroid gland carcinoma
+BMGC_DS06882,BMG_DS024707,Pigmentation Disorders
+BMGC_DS06883,BMG_DS024709,sexual dysfunction
+BMGC_DS06884,BMG_DS024712,Necrotizing Arteritis
+BMGC_DS06885,BMG_DS024713,Jackknife Seizures
+BMGC_DS06886,BMG_DS024719,Ewing sarcoma
+BMGC_DS06887,BMG_DS024720,Cafe-au-lait macules with pulmonary stenosis
+BMGC_DS06888,BMG_DS024722,Myotonic Disorders
+BMGC_DS06889,BMG_DS024726,Peritonsillar cellulitis
+BMGC_DS06890,BMG_DS024729,Hypofibrinogenemia
+BMGC_DS06891,BMG_DS024732,carcinoma
+BMGC_DS06892,BMG_DS024734,skin squamous cell carcinoma
+BMGC_DS06893,BMG_DS024735,Calcium pyrophosphate deposition disease
+BMGC_DS06894,BMG_DS024743,Olfaction Disorders
+BMGC_DS06895,BMG_DS024750,Congenital Cerebral Palsy
+BMGC_DS06896,BMG_DS024772,endomyocardial fibrosis
+BMGC_DS06897,BMG_DS024821,"Polymyositis, Idiopathic"
+BMGC_DS06898,BMG_DS024827,Synovial plica (disorder)
+BMGC_DS06899,BMG_DS024834,Group A Streptococcal Infections
+BMGC_DS06900,BMG_DS024837,Anogenital human papillomavirus infection
+BMGC_DS06901,BMG_DS024846,morpheaform basal cell carcinoma
+BMGC_DS06902,BMG_DS024848,malignant glioma
+BMGC_DS06903,BMG_DS024850,Chiari malformation type II
+BMGC_DS06904,BMG_DS024851,cystic disease of lung
+BMGC_DS06905,BMG_DS024859,Oral infection
+BMGC_DS06906,BMG_DS024884,Bacterial gastroenteritis
+BMGC_DS06907,BMG_DS024901,Uric acid renal calculus
+BMGC_DS06908,BMG_DS024961,Functional Gastrointestinal Disorders
+BMGC_DS06909,BMG_DS024971,adult spinal cord glioblastoma
+BMGC_DS06910,BMG_DS024992,cerebral neuroblastoma
+BMGC_DS06911,BMG_DS024994,adrenal gland neuroblastoma
+BMGC_DS06912,BMG_DS024995,Allergy to eggs
+BMGC_DS06913,BMG_DS024996,Allergy to peanuts
+BMGC_DS06914,BMG_DS024997,Pentalogy of Cantrell
+BMGC_DS06915,BMG_DS025021,Spinal cord syndrome
+BMGC_DS06916,BMG_DS025045,anal canal carcinoma
+BMGC_DS06917,BMG_DS025046,Viral gastritis
+BMGC_DS06918,BMG_DS025047,Acute infective exacerbation of chronic obstructive pulmonary disease
+BMGC_DS06919,BMG_DS025151,Maternal hypertension
+BMGC_DS06920,BMG_DS025163,Primary sclerosing cholangitis
+BMGC_DS06921,BMG_DS025206,Allergy to ketoprofen
+BMGC_DS06922,BMG_DS025751,Benzoic acid allergy
+BMGC_DS06923,BMG_DS025980,Allergy to formaldehyde
+BMGC_DS06924,BMG_DS026054,cephalosporin allergy
+BMGC_DS06925,BMG_DS026063,Allergy to cefaclor
+BMGC_DS06926,BMG_DS026064,Allergy to cefuroxime
+BMGC_DS06927,BMG_DS026067,Allergy to cefotaxime
+BMGC_DS06928,BMG_DS026068,Allergy to ceftazidime
+BMGC_DS06929,BMG_DS026070,Allergy to cefixime
+BMGC_DS06930,BMG_DS026073,Allergy to ceftriaxone
+BMGC_DS06931,BMG_DS026621,Guanidinoacetate methyltransferase deficiency
+BMGC_DS06932,BMG_DS026622,3-Methylglutaconic aciduria type 2
+BMGC_DS06933,BMG_DS026623,3-Methylglutaconic aciduria type 3
+BMGC_DS06934,BMG_DS026625,Generalized uridine diphosphate galactose-4-epimerase deficiency
+BMGC_DS06935,BMG_DS026626,Erythrocyte uridine diphosphate galactose-4-epimerase deficiency
+BMGC_DS06936,BMG_DS026631,Glycerol kinase deficiency - isolated
+BMGC_DS06937,BMG_DS026647,"Lesion, Superficial Radial Nerve"
+BMGC_DS06938,BMG_DS026657,Sacroiliitis
+BMGC_DS06939,BMG_DS026660,Spastic tetraparesis
+BMGC_DS06940,BMG_DS026666,thumb deformity
+BMGC_DS06941,BMG_DS026673,Nut Hypersensitivity
+BMGC_DS06942,BMG_DS026679,latex allergy
+BMGC_DS06943,BMG_DS026682,Carotid Atherosclerosis
+BMGC_DS06944,BMG_DS026693,Proteus septicemia
+BMGC_DS06945,BMG_DS026694,ureter transitional cell carcinoma
+BMGC_DS06946,BMG_DS026698,Urinary tract infection caused by Escherichia coli
+BMGC_DS06947,BMG_DS026699,Proteus urinary tract infection
+BMGC_DS06948,BMG_DS026730,Gonococcal seminal vesiculitis
+BMGC_DS06949,BMG_DS026738,Chronic Spontaneous Urticaria
+BMGC_DS06950,BMG_DS026743,Inflammation of large intestine
+BMGC_DS06951,BMG_DS026784,Recurrent sinusitis
+BMGC_DS06952,BMG_DS026802,Decompensated cardiac failure
+BMGC_DS06953,BMG_DS026804,Recurrent upper respiratory tract infection
+BMGC_DS06954,BMG_DS026808,Exacerbation of multiple sclerosis
+BMGC_DS06955,BMG_DS026809,Complete Hearing Loss
+BMGC_DS06956,BMG_DS026860,retroperitoneal sarcoma
+BMGC_DS06957,BMG_DS026863,Gastric retention
+BMGC_DS06958,BMG_DS026874,alpha-thalassemia-myelodysplastic syndrome
+BMGC_DS06959,BMG_DS026885,Hypoglossal Nerve Palsy
+BMGC_DS06960,BMG_DS026889,oral cavity squamous cell carcinoma
+BMGC_DS06961,BMG_DS026894,bone osteosarcoma
+BMGC_DS06962,BMG_DS026895,Ewing sarcoma of bone
+BMGC_DS06963,BMG_DS026896,skin pilomatrix carcinoma
+BMGC_DS06964,BMG_DS026917,epiglottis cancer
+BMGC_DS06965,BMG_DS026926,Alcohol Withdrawal Seizures
+BMGC_DS06966,BMG_DS026958,Varicella Zoster Virus Infection
+BMGC_DS06967,BMG_DS026972,Costello syndrome (disorder)
+BMGC_DS06968,BMG_DS026975,"tenosynovial giant cell tumor, localized type"
+BMGC_DS06969,BMG_DS026982,Septicemia due to enterococcus
+BMGC_DS06970,BMG_DS027011,Atypical absence seizure
+BMGC_DS06971,BMG_DS027020,laryngeal carcinoma
+BMGC_DS06972,BMG_DS027022,idiopathic scoliosis
+BMGC_DS06973,BMG_DS027024,adrenal medulla neoplasm
+BMGC_DS06974,BMG_DS027025,binge eating disorder
+BMGC_DS06975,BMG_DS027027,Cerebrovascular Occlusion
+BMGC_DS06976,BMG_DS027030,lymph node neoplasm
+BMGC_DS06977,BMG_DS027036,Hereditary protein C deficiency
+BMGC_DS06978,BMG_DS027037,Harlequin type ichthyosis
+BMGC_DS06979,BMG_DS027039,Hyperhomocysteinemia
+BMGC_DS06980,BMG_DS027041,lung sarcoma
+BMGC_DS06981,BMG_DS027042,lymphoid neoplasm
+BMGC_DS06982,BMG_DS027044,Hyperornithinemia
+BMGC_DS06983,BMG_DS027047,microphthalmia with limb anomalies
+BMGC_DS06984,BMG_DS027048,Chronic interstitial cystitis
+BMGC_DS06985,BMG_DS027049,Infective cystitis
+BMGC_DS06986,BMG_DS027051,malignant phyllodes tumor
+BMGC_DS06987,BMG_DS027052,ureter carcinoma
+BMGC_DS06988,BMG_DS027057,prostate carcinoma
+BMGC_DS06989,BMG_DS027058,External Carotid Artery Diseases
+BMGC_DS06990,BMG_DS027059,cardiac arrest
+BMGC_DS06991,BMG_DS027060,"Lung Diseases, Obstructive"
+BMGC_DS06992,BMG_DS027063,Periodontosis
+BMGC_DS06993,BMG_DS027064,Toxic Shock Syndrome
+BMGC_DS06994,BMG_DS027065,Subcorneal pustular dermatosis
+BMGC_DS06995,BMG_DS027066,Arteriosclerotic Dementia
+BMGC_DS06996,BMG_DS027067,cocaine dependence
+BMGC_DS06997,BMG_DS027068,Activated Protein C Resistance
+BMGC_DS06998,BMG_DS027069,Hepatopulmonary Syndrome
+BMGC_DS06999,BMG_DS027070,Vascular Hemostatic Disorders
+BMGC_DS07000,BMG_DS027072,choroidal neovascularization
+BMGC_DS07001,BMG_DS027074,vulvar carcinoma
+BMGC_DS07002,BMG_DS027076,Radial Tunnel Syndrome
+BMGC_DS07003,BMG_DS027077,Congenital Nephrogenic Diabetes Insipidus
+BMGC_DS07004,BMG_DS027079,Hashimoto Disease
+BMGC_DS07005,BMG_DS027081,Gastro-esophageal reflux disease with esophagitis
+BMGC_DS07006,BMG_DS027082,hereditary breast ovarian cancer syndrome
+BMGC_DS07007,BMG_DS027083,hereditary Wilms tumor
+BMGC_DS07008,BMG_DS027084,brain stem glioma
+BMGC_DS07009,BMG_DS027085,brainstem neoplasm
+BMGC_DS07010,BMG_DS027086,ovarian carcinoma
+BMGC_DS07011,BMG_DS027091,"Hyperlipidemia, group A"
+BMGC_DS07012,BMG_DS027092,Terminal Ileitis
+BMGC_DS07013,BMG_DS027093,Regional enteritis
+BMGC_DS07014,BMG_DS027094,complete hydatidiform mole
+BMGC_DS07015,BMG_DS027095,breast carcinoma
+BMGC_DS07016,BMG_DS027099,"Tuberculosis, Extrapulmonary"
+BMGC_DS07017,BMG_DS027104,depersonalization disorder
+BMGC_DS07018,BMG_DS027105,lung carcinoma
+BMGC_DS07019,BMG_DS027106,Bacterial sepsis
+BMGC_DS07020,BMG_DS027107,"Hemophilia, NOS"
+BMGC_DS07021,BMG_DS027109,tongue cancer
+BMGC_DS07022,BMG_DS027110,peripheral primitive neuroectodermal tumor
+BMGC_DS07023,BMG_DS027118,muscle cancer
+BMGC_DS07024,BMG_DS027148,hemangioma of subcutaneous tissue
+BMGC_DS07025,BMG_DS027149,splenic hemangioma
+BMGC_DS07026,BMG_DS027163,facial cleft
+BMGC_DS07027,BMG_DS027164,46 XX gonadal dysgenesis
+BMGC_DS07028,BMG_DS027165,Gonadal dysgenesis XX type deafness
+BMGC_DS07029,BMG_DS027166,familial isolated congenital asplenia
+BMGC_DS07030,BMG_DS027194,gastrointestinal system cancer
+BMGC_DS07031,BMG_DS027206,Tardive Dyskinesia
+BMGC_DS07032,BMG_DS027211,"Muscular Dystrophies, Limb-Girdle"
+BMGC_DS07033,BMG_DS027221,Marginal blepharitis
+BMGC_DS07034,BMG_DS027230,oculomotor nerve cancer
+BMGC_DS07035,BMG_DS027253,Nephronophthisis
+BMGC_DS07036,BMG_DS027254,skin hemangioma
+BMGC_DS07037,BMG_DS027255,Mineral deficiency
+BMGC_DS07038,BMG_DS027256,parathyroid gland carcinoma
+BMGC_DS07039,BMG_DS027257,Acrocephalopolysyndactyly
+BMGC_DS07040,BMG_DS027259,Central Diabetes Insipidus
+BMGC_DS07041,BMG_DS027260,Acanthocytosis
+BMGC_DS07042,BMG_DS027288,Community-Acquired Pneumonia
+BMGC_DS07043,BMG_DS027291,Disseminated atypical mycobacterial infection
+BMGC_DS07044,BMG_DS027292,Neurogenic Bowel
+BMGC_DS07045,BMG_DS027293,Hereditary Chorea
+BMGC_DS07046,BMG_DS027295,"Sensory Neuropathy, Hereditary"
+BMGC_DS07047,BMG_DS027296,Benign congenital myopathy
+BMGC_DS07048,BMG_DS027297,Congenital muscular dystrophy (disorder)
+BMGC_DS07049,BMG_DS027298,Infection of ear
+BMGC_DS07050,BMG_DS027299,colon carcinoma
+BMGC_DS07051,BMG_DS027300,gastric carcinoma
+BMGC_DS07052,BMG_DS027301,serotonin syndrome
+BMGC_DS07053,BMG_DS027304,urinary bladder carcinoma
+BMGC_DS07054,BMG_DS027305,female reproductive organ cancer
+BMGC_DS07055,BMG_DS027307,skin carcinoma
+BMGC_DS07056,BMG_DS027309,Idiopathic hypertrophic subaortic stenosis
+BMGC_DS07057,BMG_DS027311,urethra cancer
+BMGC_DS07058,BMG_DS027312,metastatic carcinoma in the bone
+BMGC_DS07059,BMG_DS027317,Viral hepatitis B without mention of hepatic coma
+BMGC_DS07060,BMG_DS027318,Pulmonary mycobacterium avium-intracellulare infection
+BMGC_DS07061,BMG_DS027319,Brachial Plexus Neuropathies
+BMGC_DS07062,BMG_DS027320,Heinz Body Anemias
+BMGC_DS07063,BMG_DS027321,Thibierge-Weissenbach syndrome
+BMGC_DS07064,BMG_DS027323,"Candidiasis, Vulvovaginal"
+BMGC_DS07065,BMG_DS027325,ependymoblastoma
+BMGC_DS07066,BMG_DS027327,Sick Headaches
+BMGC_DS07067,BMG_DS027329,congenital nystagmus
+BMGC_DS07068,BMG_DS027332,Chronic peptic ulcer
+BMGC_DS07069,BMG_DS027335,acquired hypertrophic pyloric stenosis
+BMGC_DS07070,BMG_DS027336,Radiculopathy
+BMGC_DS07071,BMG_DS027337,Spinal Muscular Atrophies of Childhood
+BMGC_DS07072,BMG_DS027339,Strudwick syndrome
+BMGC_DS07073,BMG_DS027342,inherited hypertrophic pyloric stenosis
+BMGC_DS07074,BMG_DS027350,Adrenogenital disorder
+BMGC_DS07075,BMG_DS027353,Choledocholithiasis
+BMGC_DS07076,BMG_DS027355,Disorder of thyrocalcitonin secretion
+BMGC_DS07077,BMG_DS027363,Palsy of conjugate gaze
+BMGC_DS07078,BMG_DS027366,Constitutional aplastic anemia
+BMGC_DS07079,BMG_DS027369,Acne
+BMGC_DS07080,BMG_DS027375,nasal cavity cancer
+BMGC_DS07081,BMG_DS027376,Disorder of circulatory system
+BMGC_DS07082,BMG_DS027378,appendix carcinoma
+BMGC_DS07083,BMG_DS027380,Acute peptic ulcer (disorder)
+BMGC_DS07084,BMG_DS027386,preterm premature rupture of the membranes
+BMGC_DS07085,BMG_DS027393,Bacterial respiratory infection
+BMGC_DS07086,BMG_DS027394,Bacterial upper respiratory infection
+BMGC_DS07087,BMG_DS027395,Bacterial lower respiratory infection
+BMGC_DS07088,BMG_DS027399,Bacterial urinary infection
+BMGC_DS07089,BMG_DS027410,Viral ear infection
+BMGC_DS07090,BMG_DS027413,Fungal ear infection
+BMGC_DS07091,BMG_DS027426,Floating-harbor syndrome
+BMGC_DS07092,BMG_DS027429,Infective otitis media
+BMGC_DS07093,BMG_DS027430,Infective blepharitis
+BMGC_DS07094,BMG_DS027450,Infective laryngitis
+BMGC_DS07095,BMG_DS027502,Vitreomacular traction syndrome
+BMGC_DS07096,BMG_DS027506,Severe nonproliferative diabetic retinopathy
+BMGC_DS07097,BMG_DS027513,Macular edema due to diabetes mellitus
+BMGC_DS07098,BMG_DS027518,Cone Dystrophy
+BMGC_DS07099,BMG_DS027519,Choroidal dystrophy
+BMGC_DS07100,BMG_DS027520,Macular dystrophy
+BMGC_DS07101,BMG_DS027522,North Carolina macular dystrophy
+BMGC_DS07102,BMG_DS027523,basal laminar drusen
+BMGC_DS07103,BMG_DS027530,retinal hemangioblastoma
+BMGC_DS07104,BMG_DS027532,eye lymphoma
+BMGC_DS07105,BMG_DS027558,Disorder of macula of retina
+BMGC_DS07106,BMG_DS027563,Anhydramnios
+BMGC_DS07107,BMG_DS027575,Functional visual loss
+BMGC_DS07108,BMG_DS027584,Severe chronic obstructive pulmonary disease
+BMGC_DS07109,BMG_DS027588,"Hypophosphatemic Rickets, X-Linked Dominant"
+BMGC_DS07110,BMG_DS027589,glottis carcinoma
+BMGC_DS07111,BMG_DS027591,bile duct carcinoma
+BMGC_DS07112,BMG_DS027592,myelodysplastic syndrome associated with isolated del(5q)
+BMGC_DS07113,BMG_DS027593,"Amyloidosis, Familial"
+BMGC_DS07114,BMG_DS027595,Mononeuropathy Multiplex
+BMGC_DS07115,BMG_DS027596,gastrointestinal lymphoma
+BMGC_DS07116,BMG_DS027598,Middle Cerebral Artery Thrombosis
+BMGC_DS07117,BMG_DS027599,"Aneurysm, Anterior Communicating Artery"
+BMGC_DS07118,BMG_DS027600,"Infarction, Middle Cerebral Artery"
+BMGC_DS07119,BMG_DS027601,Hyperuricemia
+BMGC_DS07120,BMG_DS027605,Acute diarrhea
+BMGC_DS07121,BMG_DS027606,Diabetic peripheral neuropathy
+BMGC_DS07122,BMG_DS027608,kidney cancer
+BMGC_DS07123,BMG_DS027609,undifferentiated high grade pleomorphic sarcoma of bone
+BMGC_DS07124,BMG_DS027610,cerebellar astrocytoma
+BMGC_DS07125,BMG_DS027611,maxillary sinus carcinoma
+BMGC_DS07126,BMG_DS027616,substance abuse
+BMGC_DS07127,BMG_DS027628,"Aortic Aneurysm, Ruptured"
+BMGC_DS07128,BMG_DS027638,Recurrent bronchitis
+BMGC_DS07129,BMG_DS027641,Cardiac Events
+BMGC_DS07130,BMG_DS027644,Cerebellar vermis atrophy
+BMGC_DS07131,BMG_DS027646,cerebritis
+BMGC_DS07132,BMG_DS027647,"Radiculopathy, Cervical"
+BMGC_DS07133,BMG_DS027650,Acute Chest Syndrome
+BMGC_DS07134,BMG_DS027658,Conus Medullaris Syndrome
+BMGC_DS07135,BMG_DS027659,Bacterial cystitis
+BMGC_DS07136,BMG_DS027662,Granulomatous dermatitis
+BMGC_DS07137,BMG_DS027666,Focal Dystonia
+BMGC_DS07138,BMG_DS027675,gastric leiomyosarcoma
+BMGC_DS07139,BMG_DS027677,Immune-complex glomerulonephritis
+BMGC_DS07140,BMG_DS027689,Chronic hiccup
+BMGC_DS07141,BMG_DS027690,osteonecrosis
+BMGC_DS07142,BMG_DS027691,Hypereosinophilia
+BMGC_DS07143,BMG_DS027692,Hyperlipoproteinemia Type IIa
+BMGC_DS07144,BMG_DS027693,Isolated Systolic Hypertension
+BMGC_DS07145,BMG_DS027694,Hypertensive emergency
+BMGC_DS07146,BMG_DS027695,Hypertensive Urgency
+BMGC_DS07147,BMG_DS027704,End Stage Liver Disease
+BMGC_DS07148,BMG_DS027708,Chronic lung disease
+BMGC_DS07149,BMG_DS027714,"Myelitis, Necrotizing"
+BMGC_DS07150,BMG_DS027715,septal myocardial infarction
+BMGC_DS07151,BMG_DS027721,Febrile Neutropenia
+BMGC_DS07152,BMG_DS027726,Recurrent otitis media
+BMGC_DS07153,BMG_DS027727,Ovarian failure
+BMGC_DS07154,BMG_DS027730,parotid gland cancer
+BMGC_DS07155,BMG_DS027732,Peroneal Neuropathies
+BMGC_DS07156,BMG_DS027747,Erythrodermic psoriasis
+BMGC_DS07157,BMG_DS027749,Radial Neuropathy
+BMGC_DS07158,BMG_DS027754,Reynolds syndrome
+BMGC_DS07159,BMG_DS027755,"HEMOLYTIC DISEASE OF FETUS AND NEWBORN, RH-INDUCED"
+BMGC_DS07160,BMG_DS027758,"Arthritis, Sacroiliac"
+BMGC_DS07161,BMG_DS027759,"Scleroderma, Limited"
+BMGC_DS07162,BMG_DS027761,sella turcica neoplasm
+BMGC_DS07163,BMG_DS027770,Submandibular abscess
+BMGC_DS07164,BMG_DS027772,supraglottis squamous cell carcinoma
+BMGC_DS07165,BMG_DS027777,athyreosis
+BMGC_DS07166,BMG_DS027778,thyroid Hurthle cell carcinoma
+BMGC_DS07167,BMG_DS027790,coumarin resistance
+BMGC_DS07168,BMG_DS027794,Cochlear Neuritis
+BMGC_DS07169,BMG_DS027795,Cochlear Nerve Diseases
+BMGC_DS07170,BMG_DS027796,Vestibular Nerve Diseases
+BMGC_DS07171,BMG_DS027797,adrenal gland cancer
+BMGC_DS07172,BMG_DS027798,"Autonomic Hyperactivity, Alcohol Withdrawal Associated"
+BMGC_DS07173,BMG_DS027799,"Alzheimer Disease, Early Onset"
+BMGC_DS07174,BMG_DS027800,"Amblyopia, Developmental"
+BMGC_DS07175,BMG_DS027801,"Amblyopia, Suppression"
+BMGC_DS07176,BMG_DS027802,"Amino Acid Metabolism, Inherited Disorders"
+BMGC_DS07177,BMG_DS027803,childhood apraxia of speech
+BMGC_DS07178,BMG_DS027804,Chiari malformation type I
+BMGC_DS07179,BMG_DS027807,cerebral astrocytoma
+BMGC_DS07180,BMG_DS027808,"Tremor, Rubral"
+BMGC_DS07181,BMG_DS027810,Peripheral Autonomic Nervous System Diseases
+BMGC_DS07182,BMG_DS027811,"Nervous System Diseases, Parasympathetic"
+BMGC_DS07183,BMG_DS027812,"Nervous System Diseases, Sympathetic"
+BMGC_DS07184,BMG_DS027813,Vertebrogenic Pain Syndrome
+BMGC_DS07185,BMG_DS027814,Lenticulostriate Disorders
+BMGC_DS07186,BMG_DS027815,biliary tract cancer
+BMGC_DS07187,BMG_DS027816,Urinary Bladder Neurogenesis
+BMGC_DS07188,BMG_DS027817,"Neurogenic Urinary Bladder, Spastic"
+BMGC_DS07189,BMG_DS027818,"Blindness, Monocular"
+BMGC_DS07190,BMG_DS027823,Central Nervous System Metabolic Disorders
+BMGC_DS07191,BMG_DS027824,primary brain neoplasm
+BMGC_DS07192,BMG_DS027825,brain cancer
+BMGC_DS07193,BMG_DS027826,Internal Carotid Artery Diseases
+BMGC_DS07194,BMG_DS027827,"Arterial Diseases, Common Carotid"
+BMGC_DS07195,BMG_DS027828,Common Carotid Artery Thrombosis
+BMGC_DS07196,BMG_DS027829,External Carotid Artery Thrombosis
+BMGC_DS07197,BMG_DS027830,Internal Carotid Artery Thrombosis
+BMGC_DS07198,BMG_DS027832,"Catatonia, Malignant"
+BMGC_DS07199,BMG_DS027834,"Aneurysm, Basilar Artery"
+BMGC_DS07200,BMG_DS027835,Brain Aneurysm
+BMGC_DS07201,BMG_DS027836,Giant Intracranial Aneurysm
+BMGC_DS07202,BMG_DS027837,"Mycotic Aneurysm, Intracranial"
+BMGC_DS07203,BMG_DS027838,Intracranial Atherosclerosis
+BMGC_DS07204,BMG_DS027839,"Cerebral Infarction, Left Hemisphere"
+BMGC_DS07205,BMG_DS027840,"Cerebral Infarction, Right Hemisphere"
+BMGC_DS07206,BMG_DS027841,Anterior Choroidal Artery Infarction
+BMGC_DS07207,BMG_DS027842,Subcortical Infarction
+BMGC_DS07208,BMG_DS027843,Carotid Circulation Transient Ischemic Attack
+BMGC_DS07209,BMG_DS027844,"Transient Ischemic Attack, Vertebrobasilar Circulation"
+BMGC_DS07210,BMG_DS027845,Crescendo Transient Ischemic Attacks
+BMGC_DS07211,BMG_DS027846,"Brain Stem Ischemia, Transient"
+BMGC_DS07212,BMG_DS027847,"Cerebral Palsy, Mixed"
+BMGC_DS07213,BMG_DS027848,"Cerebral Palsy, Rolandic Type"
+BMGC_DS07214,BMG_DS027852,Charcot-Marie-Tooth disease type 1
+BMGC_DS07215,BMG_DS027853,"Cockayne Syndrome, Type III"
+BMGC_DS07216,BMG_DS027854,"Cockayne Syndrome, Type II"
+BMGC_DS07217,BMG_DS027855,"Cockayne Syndrome, Type I"
+BMGC_DS07218,BMG_DS027856,"Color Blindness, Inherited"
+BMGC_DS07219,BMG_DS027857,Monochromatopsia
+BMGC_DS07220,BMG_DS027858,"Seizure, Febrile, Complex"
+BMGC_DS07221,BMG_DS027859,"Cranial Neuropathies, Multiple"
+BMGC_DS07222,BMG_DS027860,"Deafness, Acquired"
+BMGC_DS07223,BMG_DS027861,Diabetic Neuralgia
+BMGC_DS07224,BMG_DS027863,"Diplopia, Vertical"
+BMGC_DS07225,BMG_DS027864,"Trisomy 21, Mitotic Nondisjunction"
+BMGC_DS07226,BMG_DS027865,"Duane Retraction Syndrome, Type 2"
+BMGC_DS07227,BMG_DS027866,"Duane Retraction Syndrome, Type 3"
+BMGC_DS07228,BMG_DS027867,"Dyskinesia, Medication-Induced"
+BMGC_DS07229,BMG_DS027868,ear cancer
+BMGC_DS07230,BMG_DS027869,"Empty Sella Syndrome, Secondary"
+BMGC_DS07231,BMG_DS027871,"Encephalomyelitis, Postexanthem"
+BMGC_DS07232,BMG_DS027872,Postinfectious Encephalomyelitis
+BMGC_DS07233,BMG_DS027873,Post-Vaccinal Encephalitis
+BMGC_DS07234,BMG_DS027878,"Leukoencephalitis, Subacute Hemorrhagic"
+BMGC_DS07235,BMG_DS027879,Single Seizure
+BMGC_DS07236,BMG_DS027880,Awakening Epilepsy
+BMGC_DS07237,BMG_DS027881,Subclinical Seizure
+BMGC_DS07238,BMG_DS027882,Uncinate Seizures
+BMGC_DS07239,BMG_DS027883,Digestive Epilepsy
+BMGC_DS07240,BMG_DS027884,Cryptogenic Tonic-Clonic Epilepsy
+BMGC_DS07241,BMG_DS027885,"Epilepsy, Tonic-Clonic, Familial"
+BMGC_DS07242,BMG_DS027886,"Epilepsy, Tonic-Clonic, Symptomatic"
+BMGC_DS07243,BMG_DS027887,Benign Infantile Myoclonic Epilepsy
+BMGC_DS07244,BMG_DS027888,Infantile Severe Myoclonic Epilepsy
+BMGC_DS07245,BMG_DS027889,Atonic Absence Seizures
+BMGC_DS07246,BMG_DS027890,"Epilepsy, Absence, Atypical"
+BMGC_DS07247,BMG_DS027892,Facial Neuritis
+BMGC_DS07248,BMG_DS027893,Familial Facial Neuropathy
+BMGC_DS07249,BMG_DS027894,Acquired Facial Neuropathy
+BMGC_DS07250,BMG_DS027896,"Fibromyalgia, Primary"
+BMGC_DS07251,BMG_DS027897,"Fibromyalgia, Secondary"
+BMGC_DS07252,BMG_DS027898,FRAXA Syndrome
+BMGC_DS07253,BMG_DS027899,FRAXE Syndrome
+BMGC_DS07254,BMG_DS027900,galactose epimerase deficiency
+BMGC_DS07255,BMG_DS027902,Adult Glycogen Storage Disease Type II
+BMGC_DS07256,BMG_DS027903,"Glycogen Storage Disease Type II, Infantile"
+BMGC_DS07257,BMG_DS027904,"Glycogen Storage Disease Type II, Juvenile"
+BMGC_DS07258,BMG_DS027905,Primary Cough Headache
+BMGC_DS07259,BMG_DS027906,Fulminant Hepatic Failure with Cerebral Edema
+BMGC_DS07260,BMG_DS027907,Hepatic Stupor
+BMGC_DS07261,BMG_DS027908,Cystathionine beta-Synthase Deficiency Disease
+BMGC_DS07262,BMG_DS027913,Akinetic-Rigid Variant of Huntington Disease
+BMGC_DS07263,BMG_DS027914,Juvenile Huntington Disease
+BMGC_DS07264,BMG_DS027915,Inappropriate ACTH Secretion Syndrome
+BMGC_DS07265,BMG_DS027919,"Hypersomnia, Recurrent"
+BMGC_DS07266,BMG_DS027920,"Hypersomnolence Disorders, Primary"
+BMGC_DS07267,BMG_DS027921,"Hypersomnolence Disorders, Secondary"
+BMGC_DS07268,BMG_DS027922,Hypothalamic Dysfunction Syndromes
+BMGC_DS07269,BMG_DS027923,Hypothalamic Dysinhibition Syndrome
+BMGC_DS07270,BMG_DS027924,Hypothalamic Overactivity Syndrome
+BMGC_DS07271,BMG_DS027925,Hypothalamic-Adenohypophyseal Disorders
+BMGC_DS07272,BMG_DS027926,Hypothalamic-Neurohypophyseal Disorders
+BMGC_DS07273,BMG_DS027927,Pituitary Diencephalic Syndrome
+BMGC_DS07274,BMG_DS027928,Chronic Insomnia
+BMGC_DS07275,BMG_DS027929,Psychophysiological Insomnia
+BMGC_DS07276,BMG_DS027930,Sleep Initiation Dysfunction
+BMGC_DS07277,BMG_DS027931,"Creutzfeldt-Jakob Disease, Familial"
+BMGC_DS07278,BMG_DS027933,"Auditory Processing Disorder, Central"
+BMGC_DS07279,BMG_DS027934,learning disability
+BMGC_DS07280,BMG_DS027935,"Encephalopathy, Subacute Necrotizing, Infantile"
+BMGC_DS07281,BMG_DS027936,"Encephalopathy, Subacute Necrotizing, Juvenile"
+BMGC_DS07282,BMG_DS027937,Infantile Globoid Cell Leukodystrophy
+BMGC_DS07283,BMG_DS027938,"Metachromatic leukodystrophy, juvenile type"
+BMGC_DS07284,BMG_DS027939,"Metachromatic Leukodystrophy, Infant"
+BMGC_DS07285,BMG_DS027940,"Leukodystrophy, Metachromatic, Adult"
+BMGC_DS07286,BMG_DS027942,"Maple Syrup Urine Disease, Thiamine Responsive"
+BMGC_DS07287,BMG_DS027943,desmoplastic/nodular medulloblastoma
+BMGC_DS07288,BMG_DS027944,cerebral convexity meningioma
+BMGC_DS07289,BMG_DS027945,parasagittal meningioma
+BMGC_DS07290,BMG_DS027946,"Meningitis, Haemophilus parainfluenzae"
+BMGC_DS07291,BMG_DS027947,"Meningitis, Haemophilus influenzae Type F"
+BMGC_DS07292,BMG_DS027948,"Meningitis, Pneumococcal, Penicillin-Resistant"
+BMGC_DS07293,BMG_DS027949,myelomeningocele
+BMGC_DS07294,BMG_DS027950,"Moyamoya Disease, Primary"
+BMGC_DS07295,BMG_DS027951,"Moyamoya Disease, Secondary"
+BMGC_DS07296,BMG_DS027952,"Multiple Sclerosis, Acute Fulminating"
+BMGC_DS07297,BMG_DS027953,Progressive Proximal Myelopathic Muscular Atrophy
+BMGC_DS07298,BMG_DS027954,Scapuloperoneal Form of Spinal Muscular Atrophy
+BMGC_DS07299,BMG_DS027955,Distal Muscular Dystrophies
+BMGC_DS07300,BMG_DS027956,X-Linked Emery-Dreifuss Muscular Dystrophy
+BMGC_DS07301,BMG_DS027957,"Myasthenia Gravis, Generalized"
+BMGC_DS07302,BMG_DS027958,"Myasthenia Gravis, Ocular"
+BMGC_DS07303,BMG_DS027960,"Myelitis, Paraneoplastic"
+BMGC_DS07304,BMG_DS027961,"Myelitis, Postinfectious"
+BMGC_DS07305,BMG_DS027962,"Myelitis, Postvaccinal"
+BMGC_DS07306,BMG_DS027963,"Myelitis, Subacute Transverse"
+BMGC_DS07307,BMG_DS027964,Demyelinative Myelitis
+BMGC_DS07308,BMG_DS027965,"Myoclonus, Eyelid"
+BMGC_DS07309,BMG_DS027966,Idiopathic Inflammatory Myopathies
+BMGC_DS07310,BMG_DS027967,"Myositis, Focal"
+BMGC_DS07311,BMG_DS027968,Becker Generalized Myotonia
+BMGC_DS07312,BMG_DS027969,Narcolepsy-Cataplexy Syndrome
+BMGC_DS07313,BMG_DS027970,External Nerve Compression Syndromes
+BMGC_DS07314,BMG_DS027971,Internal Nerve Compression Syndromes
+BMGC_DS07315,BMG_DS027972,Neuroleptic-Induced Neuroleptic Malignant Syndrome
+BMGC_DS07316,BMG_DS027973,Foley-Denny-Brown Syndrome
+BMGC_DS07317,BMG_DS027974,Juvenile Neuronal Ceroid Lipofuscinosis
+BMGC_DS07318,BMG_DS027975,oligodendroglioma
+BMGC_DS07319,BMG_DS027979,Optic Disk Disorders
+BMGC_DS07320,BMG_DS027980,Post-Traumatic Osteoporosis
+BMGC_DS07321,BMG_DS027982,"Parkinson Disease, Secondary Vascular"
+BMGC_DS07322,BMG_DS027983,Atherosclerotic Parkinsonism
+BMGC_DS07323,BMG_DS027984,Hereditary Autoinflammatory Diseases
+BMGC_DS07324,BMG_DS027987,Classical phenylketonuria
+BMGC_DS07325,BMG_DS027988,Hyperphenylalaninaemia
+BMGC_DS07326,BMG_DS027989,"Hyperphenylalaninemia, Non-Phenylketonuric"
+BMGC_DS07327,BMG_DS027990,Adenohypophyseal Diseases
+BMGC_DS07328,BMG_DS027994,"Encephalitis, Polio"
+BMGC_DS07329,BMG_DS027995,"Poliomyelitis, Nonpoliovirus"
+BMGC_DS07330,BMG_DS027996,"Poliomyelitis, Preparalytic"
+BMGC_DS07331,BMG_DS027997,"Polyneuropathy, Familial"
+BMGC_DS07332,BMG_DS027998,Acquired Polyneuropathy
+BMGC_DS07333,BMG_DS028000,Flaccid Quadriplegia
+BMGC_DS07334,BMG_DS028001,"Paralysis, Spinal, Quadriplegic"
+BMGC_DS07335,BMG_DS028002,Nerve Root Compression
+BMGC_DS07336,BMG_DS028003,hereditary retinoblastoma
+BMGC_DS07337,BMG_DS028004,"Reye Syndrome, Adult"
+BMGC_DS07338,BMG_DS028005,Reye-Like Syndrome
+BMGC_DS07339,BMG_DS028006,Adult Sandhoff Disease
+BMGC_DS07340,BMG_DS028007,Infantile Sandhoff Disease
+BMGC_DS07341,BMG_DS028008,Juvenile Sandhoff Disease
+BMGC_DS07342,BMG_DS028009,"Seizures, Focal"
+BMGC_DS07343,BMG_DS028010,Special Senses Disorders
+BMGC_DS07344,BMG_DS028011,Petrous Sinus Thrombophlebitis
+BMGC_DS07345,BMG_DS028012,Intracranial Sinus Thrombophlebitis
+BMGC_DS07346,BMG_DS028013,Petrous Sinus Thrombosis
+BMGC_DS07347,BMG_DS028014,Insufficient Sleep Syndrome
+BMGC_DS07348,BMG_DS028015,REM Sleep Deprivation
+BMGC_DS07349,BMG_DS028016,Sleep-Related Neurogenic Tachypnea
+BMGC_DS07350,BMG_DS028017,Verbal Fluency Disorders
+BMGC_DS07351,BMG_DS028018,"Status Epilepticus, Subclinical"
+BMGC_DS07352,BMG_DS028019,Non-Convulsive Status Epilepticus
+BMGC_DS07353,BMG_DS028020,Simple Partial Status Epilepticus
+BMGC_DS07354,BMG_DS028021,Convergent Comitant Strabismus
+BMGC_DS07355,BMG_DS028022,"Strabismus, Noncomitant"
+BMGC_DS07356,BMG_DS028023,stuttering
+BMGC_DS07357,BMG_DS028024,stuttering
+BMGC_DS07358,BMG_DS028025,stuttering
+BMGC_DS07359,BMG_DS028029,"Syncope, Deglutitional"
+BMGC_DS07360,BMG_DS028030,"Syncope, Hyperventilation"
+BMGC_DS07361,BMG_DS028031,"Syncope, Stokes-Adams"
+BMGC_DS07362,BMG_DS028034,Tangier Disease Neuropathy
+BMGC_DS07363,BMG_DS028035,Giant Cell Aortic Arteritis
+BMGC_DS07364,BMG_DS028036,Juvenile Temporal Arteritis
+BMGC_DS07365,BMG_DS028040,thymus cancer
+BMGC_DS07366,BMG_DS028041,Childhood Tic Disorders
+BMGC_DS07367,BMG_DS028042,Motor Tic Disorders
+BMGC_DS07368,BMG_DS028043,Pulsatile Tinnitus
+BMGC_DS07369,BMG_DS028044,tonsil cancer
+BMGC_DS07370,BMG_DS028047,Vertebrobasilar Dolichoectasia
+BMGC_DS07371,BMG_DS028051,"Encephalitis, West Nile Fever"
+BMGC_DS07372,BMG_DS028052,West Nile Fever Meningitis
+BMGC_DS07373,BMG_DS028053,West Nile Fever Meningoencephalitis
+BMGC_DS07374,BMG_DS028054,West Nile Fever Myelitis
+BMGC_DS07375,BMG_DS028055,cerebral arteriopathy with subcortical infarcts and leukoencephalopathy
+BMGC_DS07376,BMG_DS028056,supratentorial cancer
+BMGC_DS07377,BMG_DS028057,infratentorial cancer
+BMGC_DS07378,BMG_DS028058,Zellweger-Like Syndrome
+BMGC_DS07379,BMG_DS028059,Juvenile Pyruvate Dehydrogenase Complex Deficiency Disease
+BMGC_DS07380,BMG_DS028060,"Pyruvate Dehydrogenase Complex Deficiency Disease, Neonatal"
+BMGC_DS07381,BMG_DS028061,"Ataxia with Lactic Acidosis, Type I"
+BMGC_DS07382,BMG_DS028062,Hereditary Autosomal Dominant Spastic Paraplegia
+BMGC_DS07383,BMG_DS028063,Autosomal Recessive Hereditary Spastic Paraplegia
+BMGC_DS07384,BMG_DS028064,Hereditary X-Linked Recessive Spastic Paraplegia
+BMGC_DS07385,BMG_DS028065,"X-Linked, Spastic Paraplegia, Hereditary"
+BMGC_DS07386,BMG_DS028066,adult acute lymphoblastic leukemia
+BMGC_DS07387,BMG_DS028068,"Eosinophilia-Myalgia Syndrome, L-Tryptophan-Related"
+BMGC_DS07388,BMG_DS028070,"Toxoplasmosis, Central Nervous System"
+BMGC_DS07389,BMG_DS028071,Intracranial Toxoplasmosis
+BMGC_DS07390,BMG_DS028072,Neurotoxoplasmosis
+BMGC_DS07391,BMG_DS028073,Common Carotid Artery Stenosis
+BMGC_DS07392,BMG_DS028074,External Carotid Artery Stenosis
+BMGC_DS07393,BMG_DS028075,Granulomous Cerebral Cryptococcosis
+BMGC_DS07394,BMG_DS028077,Cryptogenic Partial Complex Epilepsy
+BMGC_DS07395,BMG_DS028078,"Epilepsy, Symptomatic, Partial Complex"
+BMGC_DS07396,BMG_DS028079,"Epilepsy, Anterior Fronto-Polar"
+BMGC_DS07397,BMG_DS028080,"Epilepsy, Orbito-Frontal"
+BMGC_DS07398,BMG_DS028081,"Human Transmissible Spongiform Encephalopathies, Inherited"
+BMGC_DS07399,BMG_DS028082,Pseudoakathisia
+BMGC_DS07400,BMG_DS028083,Mitochondrial Diseases
+BMGC_DS07401,BMG_DS028088,"Amyloid Neuropathy, Secondary"
+BMGC_DS07402,BMG_DS028089,"Canavan Disease, Familial Form"
+BMGC_DS07403,BMG_DS028090,"Canavan Disease, Neonatal"
+BMGC_DS07404,BMG_DS028091,"Canavan Disease, Sporadic Form"
+BMGC_DS07405,BMG_DS028092,"Canavan Disease, Infantile"
+BMGC_DS07406,BMG_DS028093,"Canavan Disease, Juvenile"
+BMGC_DS07407,BMG_DS028094,Machado-Joseph Disease Type I
+BMGC_DS07408,BMG_DS028095,Machado-Joseph Disease Type II
+BMGC_DS07409,BMG_DS028096,Machado-Joseph Disease Type III
+BMGC_DS07410,BMG_DS028097,Machado-Joseph Disease Type IV
+BMGC_DS07411,BMG_DS028098,lymphangioleiomyomatosis
+BMGC_DS07412,BMG_DS028099,cerebral primitive neuroectodermal tumor
+BMGC_DS07413,BMG_DS028100,squamous cell carcinoma
+BMGC_DS07414,BMG_DS028101,peripheral nerve sheath neoplasm
+BMGC_DS07415,BMG_DS028102,malignant peripheral nerve sheath tumor
+BMGC_DS07416,BMG_DS028103,perineurioma
+BMGC_DS07417,BMG_DS028104,Brown-Sequard's Paralysis
+BMGC_DS07418,BMG_DS028105,Spastic Spinal Monoplegia Syndrome
+BMGC_DS07419,BMG_DS028112,Tension-Vascular Headache
+BMGC_DS07420,BMG_DS028113,progressive non-fluent aphasia
+BMGC_DS07421,BMG_DS028114,"Peroxisomal Dysfunction, General"
+BMGC_DS07422,BMG_DS028115,"Peroxisomal Dysfunction, Multiple"
+BMGC_DS07423,BMG_DS028116,"Peroxisomal Dysfunction, Single"
+BMGC_DS07424,BMG_DS028117,Anterior Ischemic Optic Neuropathy
+BMGC_DS07425,BMG_DS028118,Posterior Ischemic Optic Neuropathy
+BMGC_DS07426,BMG_DS028119,"Inclusion Body Myopathy, Sporadic"
+BMGC_DS07427,BMG_DS028120,Adult Neuroaxonal Dystrophy
+BMGC_DS07428,BMG_DS028121,Juvenile Neuroaxonal Dystrophy
+BMGC_DS07429,BMG_DS028122,Late Infantile Neuroaxonal Dystrophy
+BMGC_DS07430,BMG_DS028126,"Blindness, Cortical, Post-Ictal"
+BMGC_DS07431,BMG_DS028127,Anton Syndrome
+BMGC_DS07432,BMG_DS028130,"Degenerative Diseases, Spinal Cord"
+BMGC_DS07433,BMG_DS028132,Basal Ganglia Cerebrovascular Disease
+BMGC_DS07434,BMG_DS028133,Lenticulostriate Vasculopathy
+BMGC_DS07435,BMG_DS028134,"Metabolic Disorder, Central Nervous System, Acquired"
+BMGC_DS07436,BMG_DS028135,"Brain Diseases, Metabolic, Acquired"
+BMGC_DS07437,BMG_DS028137,"Hyperglycinemia, Nonketotic, Type III"
+BMGC_DS07438,BMG_DS028138,Nonketotic Hyperglycinemia
+BMGC_DS07439,BMG_DS028139,"Argininosuccinic Acid Synthetase Deficiency Disease, Partial"
+BMGC_DS07440,BMG_DS028140,"Argininosuccinic Acid Synthetase Deficiency, Complete"
+BMGC_DS07441,BMG_DS028141,Carbamoyl-Phosphate Synthase I Deficiency Disease
+BMGC_DS07442,BMG_DS028143,Advanced Sleep Phase Syndrome
+BMGC_DS07443,BMG_DS028145,Upper Airway Resistance Sleep Apnea Syndrome
+BMGC_DS07444,BMG_DS028146,"Central Sleep Apnea, Primary"
+BMGC_DS07445,BMG_DS028147,"Central Sleep Apnea, Secondary"
+BMGC_DS07446,BMG_DS028151,REM sleep behavior disorder
+BMGC_DS07447,BMG_DS028152,Nocturnal Myoclonus Syndrome
+BMGC_DS07448,BMG_DS028153,Atypical Inclusion-Body Disease
+BMGC_DS07449,BMG_DS028154,Familial Progressive Myoclonic Epilepsy
+BMGC_DS07450,BMG_DS028155,"Myoclonic Epilepsies, Progressive"
+BMGC_DS07451,BMG_DS028156,Action Myoclonus-Renal Failure Syndrome
+BMGC_DS07452,BMG_DS028157,Biotin-Responsive Encephalopathy
+BMGC_DS07453,BMG_DS028158,Dentatorubral-Pallidoluysian Atrophy
+BMGC_DS07454,BMG_DS028159,May-White Syndrome
+BMGC_DS07455,BMG_DS028160,Lafora Disease
+BMGC_DS07456,BMG_DS028161,"Lafora Body Disease, Late Onset"
+BMGC_DS07457,BMG_DS028162,Unverricht-Lundborg Syndrome
+BMGC_DS07458,BMG_DS028163,Decision Making Reflex Epilepsy
+BMGC_DS07459,BMG_DS028164,"Reflex Epilepsy, Eating-Induced"
+BMGC_DS07460,BMG_DS028165,"Reflex Epilepsy, Visual Pattern"
+BMGC_DS07461,BMG_DS028166,Tactile Reflex Epilepsy
+BMGC_DS07462,BMG_DS028167,Writing-Induced Reflex Epilepsy
+BMGC_DS07463,BMG_DS028168,"Reflex Epilepsy, Audiogenic"
+BMGC_DS07464,BMG_DS028169,"Coma, Post-Traumatic, Prolonged"
+BMGC_DS07465,BMG_DS028170,"Carotid Artery, Internal, Dissection"
+BMGC_DS07466,BMG_DS028173,"Septic Phlebitis, Sagittal Sinus"
+BMGC_DS07467,BMG_DS028174,Sagittal Sinus Thrombophlebitis
+BMGC_DS07468,BMG_DS028175,"Septic Phlebitis, Cavernous Sinus"
+BMGC_DS07469,BMG_DS028178,"Gait Disorder, Sensorimotor"
+BMGC_DS07470,BMG_DS028179,"Gait Disorders, Neurologic"
+BMGC_DS07471,BMG_DS028183,"Infarction, Anterior Cerebral Artery"
+BMGC_DS07472,BMG_DS028185,Middle Cerebral Artery Embolus
+BMGC_DS07473,BMG_DS028186,Left Middle Cerebral Artery Infarction
+BMGC_DS07474,BMG_DS028187,"Embolic Infarction, Middle Cerebral Artery"
+BMGC_DS07475,BMG_DS028188,"Thrombotic Infarction, Middle Cerebral Artery"
+BMGC_DS07476,BMG_DS028189,Right Middle Cerebral Artery Infarction
+BMGC_DS07477,BMG_DS028190,Arsenic Encephalopathy
+BMGC_DS07478,BMG_DS028191,Mercurial Neuroanesthenia
+BMGC_DS07479,BMG_DS028192,"Lead Encephalopathy, Childhood"
+BMGC_DS07480,BMG_DS028193,Lead Polyneuropathy
+BMGC_DS07481,BMG_DS028194,MPTP-Induced Degeneration of the Striatum
+BMGC_DS07482,BMG_DS028195,"Alcohol-Induced Disorders, Nervous System"
+BMGC_DS07483,BMG_DS028197,Alcohol Withdrawal-Induced Major Motor Seizure
+BMGC_DS07484,BMG_DS028198,"Status Epilepticus, Alcohol Withdrawal-Induced"
+BMGC_DS07485,BMG_DS028199,"Heredodegenerative Disorders, Nervous System"
+BMGC_DS07486,BMG_DS028200,Autoimmune Diseases of the Nervous System
+BMGC_DS07487,BMG_DS028201,"Immune Disorders, Nervous System"
+BMGC_DS07488,BMG_DS028206,"Vasculitis, Central Nervous System"
+BMGC_DS07489,BMG_DS028207,Secondary CNS Vasculitis
+BMGC_DS07490,BMG_DS028208,Postzoster Arteritis
+BMGC_DS07491,BMG_DS028209,Primary CNS Vasculitis
+BMGC_DS07492,BMG_DS028210,"Myasthenic Syndromes, Congenital"
+BMGC_DS07493,BMG_DS028211,"Congenital Myasthenic Syndromes, Postsynaptic"
+BMGC_DS07494,BMG_DS028212,"Congenital Myasthenic Syndromes, Presynaptic"
+BMGC_DS07495,BMG_DS028213,"Myasthenic Syndromes, Congenital, Slow Channel"
+BMGC_DS07496,BMG_DS028214,brain stem cancer
+BMGC_DS07497,BMG_DS028215,"Vasospasm, Intracranial"
+BMGC_DS07498,BMG_DS028216,Migraine with Acute Onset Aura
+BMGC_DS07499,BMG_DS028218,Subacute Vestibular Neuritis
+BMGC_DS07500,BMG_DS028219,Vestibular Neuronitis
+BMGC_DS07501,BMG_DS028220,Vestibular Neuropathy
+BMGC_DS07502,BMG_DS028224,Adult Pelizaeus-Merzbacher Disease
+BMGC_DS07503,BMG_DS028225,"Pelizaeus-Merzbacher Disease, Atypical"
+BMGC_DS07504,BMG_DS028226,Classic Pelizaeus-Merzbacher Disease
+BMGC_DS07505,BMG_DS028227,"Pelizaeus-Merzbacher Disease, Transitional"
+BMGC_DS07506,BMG_DS028228,Cockayne-Pelizaeus-Merzbacher Disease
+BMGC_DS07507,BMG_DS028229,Acquired Neuromyotonia
+BMGC_DS07508,BMG_DS028230,"Medial Neuropathy, Distal"
+BMGC_DS07509,BMG_DS028231,Median Neuropathy
+BMGC_DS07510,BMG_DS028232,"Neuralgia-Neuritis, Sciatic Nerve"
+BMGC_DS07511,BMG_DS028233,Sciatic Nerve Palsy
+BMGC_DS07512,BMG_DS028234,"Neuropathy, Common Peroneal"
+BMGC_DS07513,BMG_DS028235,Fibular Neuropathy
+BMGC_DS07514,BMG_DS028236,"Neuropathy, Deep Peroneal"
+BMGC_DS07515,BMG_DS028237,"Neuropathy, Superficial Peroneal"
+BMGC_DS07516,BMG_DS028238,Femoral Neuritis
+BMGC_DS07517,BMG_DS028239,Femoral Neuropathy
+BMGC_DS07518,BMG_DS028240,Tibial Neuropathy
+BMGC_DS07519,BMG_DS028245,olfactory nerve disorder
+BMGC_DS07520,BMG_DS028246,"Superior Oblique Palsy, Neurogenic"
+BMGC_DS07521,BMG_DS028247,"Abducens Palsy, Childhood, Benign Recurrent"
+BMGC_DS07522,BMG_DS028249,Glossopharyngeal Motor Neuropathy
+BMGC_DS07523,BMG_DS028252,Hypoglossal Neuropathy
+BMGC_DS07524,BMG_DS028253,"Neonatal Sleep Myoclonus, Benign"
+BMGC_DS07525,BMG_DS028254,Sleep-Related Abnormal Swallowing Syndrome
+BMGC_DS07526,BMG_DS028255,Neuromuscular Junction Diseases
+BMGC_DS07527,BMG_DS028256,"Myopathy, Central Core"
+BMGC_DS07528,BMG_DS028257,Anterior Circulation Brain Infarction
+BMGC_DS07529,BMG_DS028258,"Brain Infarction, Posterior Circulation"
+BMGC_DS07530,BMG_DS028259,"Venous Infarction, Brain"
+BMGC_DS07531,BMG_DS028260,Brain Infarction
+BMGC_DS07532,BMG_DS028261,Acute Cerebrovascular Accidents
+BMGC_DS07533,BMG_DS028262,"Lymphoma, Lymphocytic, Intermediate"
+BMGC_DS07534,BMG_DS028263,Millard-Gublar Syndrome
+BMGC_DS07535,BMG_DS028264,"Multiple Sclerosis, Primary Progressive"
+BMGC_DS07536,BMG_DS028265,"Multiple Sclerosis, Secondary Progressive"
+BMGC_DS07537,BMG_DS028266,"Multiple Sclerosis, Relapsing-Remitting"
+BMGC_DS07538,BMG_DS028267,Hypocatalasemia
+BMGC_DS07539,BMG_DS028268,Autosomal Dominant Juvenile Parkinson Disease
+BMGC_DS07540,BMG_DS028269,Autosomal Dominant Parkinsonism
+BMGC_DS07541,BMG_DS028270,Autosomal Recessive Parkinsonism
+BMGC_DS07542,BMG_DS028271,Familial Juvenile Parkinsonism
+BMGC_DS07543,BMG_DS028272,"Parkinsonism, Juvenile"
+BMGC_DS07544,BMG_DS028273,"Brain Diseases, Metabolic, Inherited"
+BMGC_DS07545,BMG_DS028274,"Brain Diseases, Metabolic, Inborn"
+BMGC_DS07546,BMG_DS028275,Central Nervous System Inborn Metabolic Diseases
+BMGC_DS07547,BMG_DS028276,Spinocerebellar Ataxia Type 1
+BMGC_DS07548,BMG_DS028277,Spinocerebellar Ataxia Type 2
+BMGC_DS07549,BMG_DS028278,Spinocerebellar Ataxia Type 4
+BMGC_DS07550,BMG_DS028279,Spinocerebellar Ataxia Type 5
+BMGC_DS07551,BMG_DS028280,spinocerebellar ataxia type 6
+BMGC_DS07552,BMG_DS028281,Spinocerebellar Ataxia Type 7
+BMGC_DS07553,BMG_DS028282,Spinal Cord Vascular Diseases
+BMGC_DS07554,BMG_DS028283,Posterior Spinal Artery Syndrome
+BMGC_DS07555,BMG_DS028284,Spinal Cord Ischemia
+BMGC_DS07556,BMG_DS028285,"Infarction, Posterior Cerebral Artery"
+BMGC_DS07557,BMG_DS028286,"Embolic Infarction, Posterior Cerebral Artery"
+BMGC_DS07558,BMG_DS028287,"Thrombotic Infarction, Posterior Cerebral Artery"
+BMGC_DS07559,BMG_DS028288,"Brain Diseases, Arterial"
+BMGC_DS07560,BMG_DS028289,Intracranial Arterial Diseases
+BMGC_DS07561,BMG_DS028290,Intracranial Embolism
+BMGC_DS07562,BMG_DS028291,Intracranial Thrombosis
+BMGC_DS07563,BMG_DS028292,Brain Thrombosis
+BMGC_DS07564,BMG_DS028294,Chronic Daily Headache
+BMGC_DS07565,BMG_DS028295,"Headache, Intractable"
+BMGC_DS07566,BMG_DS028296,Hypnic Headache
+BMGC_DS07567,BMG_DS028298,Bardet-Biedl Syndrome
+BMGC_DS07568,BMG_DS028306,Neuroschistosomiasis
+BMGC_DS07569,BMG_DS028311,Ballismus
+BMGC_DS07570,BMG_DS028312,Adult-Onset Dystonias
+BMGC_DS07571,BMG_DS028313,Adult-Onset Idiopathic Focal Dystonias
+BMGC_DS07572,BMG_DS028314,Adult-Onset Idiopathic Torsion Dystonias
+BMGC_DS07573,BMG_DS028315,Autosomal Dominant Familial Dystonia
+BMGC_DS07574,BMG_DS028316,Autosomal Recessive Familial Dystonia
+BMGC_DS07575,BMG_DS028317,Childhood Onset Dystonias
+BMGC_DS07576,BMG_DS028318,"Dystonia, Primary"
+BMGC_DS07577,BMG_DS028319,"Dystonia, Secondary"
+BMGC_DS07578,BMG_DS028320,"Dystonias, Sporadic"
+BMGC_DS07579,BMG_DS028321,Familial Dystonia
+BMGC_DS07580,BMG_DS028322,Pseudodystonia
+BMGC_DS07581,BMG_DS028323,"Dyskinesias, Paroxysmal"
+BMGC_DS07582,BMG_DS028326,Lyme Neuroborreliosis
+BMGC_DS07583,BMG_DS028333,Position Sense Disorders
+BMGC_DS07584,BMG_DS028334,Thermal Sensation Disorders
+BMGC_DS07585,BMG_DS028335,Somatosensory Disorders
+BMGC_DS07586,BMG_DS028336,Congenital Structural Myopathy
+BMGC_DS07587,BMG_DS028339,Environmental Sleep Disorder
+BMGC_DS07588,BMG_DS028340,"Sleep Disorders, Extrinsic"
+BMGC_DS07589,BMG_DS028348,Hypoxic-Ischemic Encephalopathy
+BMGC_DS07590,BMG_DS028349,Anoxic-Ischemic Encephalopathy
+BMGC_DS07591,BMG_DS028350,"Anoxia-Ischemia, Brain"
+BMGC_DS07592,BMG_DS028351,"Anoxia-Ischemia, Cerebral"
+BMGC_DS07593,BMG_DS028352,"Hypoxia-Ischemia, Brain"
+BMGC_DS07594,BMG_DS028353,"Epilepsy, Partial, Sensory"
+BMGC_DS07595,BMG_DS028354,Focal Clonic Seizures
+BMGC_DS07596,BMG_DS028361,"Lupus Vasculitis, Central Nervous System"
+BMGC_DS07597,BMG_DS028362,Lupus Meningoencephalitis
+BMGC_DS07598,BMG_DS028363,Neuropsychiatric Systemic Lupus Erythematosus
+BMGC_DS07599,BMG_DS028365,Neuroaspergillosis
+BMGC_DS07600,BMG_DS028366,Lewy Body Disease
+BMGC_DS07601,BMG_DS028367,"Muscular Disorders, Atrophic"
+BMGC_DS07602,BMG_DS028369,myotonia fluctuans
+BMGC_DS07603,BMG_DS028373,Cerebral arterial thrombosis
+BMGC_DS07604,BMG_DS028374,omphalocele
+BMGC_DS07605,BMG_DS028391,Recombinant chromosome 8 syndrome
+BMGC_DS07606,BMG_DS028396,CHROMOSOME 9p DELETION SYNDROME
+BMGC_DS07607,BMG_DS028398,KLEEFSTRA SYNDROME 1
+BMGC_DS07608,BMG_DS028403,Jacobsen Distal 11q Deletion Syndrome
+BMGC_DS07609,BMG_DS028416,Smith-Magenis syndrome
+BMGC_DS07610,BMG_DS028426,"autism, susceptibility to, X-linked 4"
+BMGC_DS07611,BMG_DS028427,Allan-Herndon-Dudley syndrome
+BMGC_DS07612,BMG_DS028429,Alopecia contractures dwarfism mental retardation
+BMGC_DS07613,BMG_DS028430,Cleft Palate-Lateral Synechia Syndrome
+BMGC_DS07614,BMG_DS028432,"Coloboma, cleft lip-palate and mental retardation syndrome"
+BMGC_DS07615,BMG_DS028433,Cantu syndrome
+BMGC_DS07616,BMG_DS028434,CONOTRUNCAL ANOMALY FACE SYNDROME
+BMGC_DS07617,BMG_DS028435,COWCHOCK SYNDROME
+BMGC_DS07618,BMG_DS028436,Crome syndrome
+BMGC_DS07619,BMG_DS028437,Winter Shortland Temple syndrome
+BMGC_DS07620,BMG_DS028438,"Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type"
+BMGC_DS07621,BMG_DS028440,"Deafness, congenital onychodystrophy, recessive form"
+BMGC_DS07622,BMG_DS028441,Edinburgh Malformation Syndrome
+BMGC_DS07623,BMG_DS028442,Digitorenocerebral Syndrome
+BMGC_DS07624,BMG_DS028444,AMINOPTERIN SYNDROME SINE AMINOPTERIN
+BMGC_DS07625,BMG_DS028445,Filippi syndrome
+BMGC_DS07626,BMG_DS028446,Fine-Lubinsky syndrome
+BMGC_DS07627,BMG_DS028448,Fountain syndrome
+BMGC_DS07628,BMG_DS028450,Galloway Mowat syndrome
+BMGC_DS07629,BMG_DS028451,Corpus callosum agenesis neuronopathy
+BMGC_DS07630,BMG_DS028452,XK aprosencephaly
+BMGC_DS07631,BMG_DS028453,MASA syndrome
+BMGC_DS07632,BMG_DS028454,Chylomicron retention disease
+BMGC_DS07633,BMG_DS028455,Gomez Lopez Hernandez syndrome
+BMGC_DS07634,BMG_DS028456,X-linked mental retardation Gustavson type
+BMGC_DS07635,BMG_DS028457,Hardikar syndrome
+BMGC_DS07636,BMG_DS028459,"bullous dystrophy, macular type"
+BMGC_DS07637,BMG_DS028462,Infantile striatonigral degeneration
+BMGC_DS07638,BMG_DS028463,JACKSON-WEISS SYNDROME
+BMGC_DS07639,BMG_DS028467,Juberg-Marsidi syndrome
+BMGC_DS07640,BMG_DS028468,Kabuki syndrome
+BMGC_DS07641,BMG_DS028469,Kapur Toriello syndrome
+BMGC_DS07642,BMG_DS028470,Kifafa seizure disorder
+BMGC_DS07643,BMG_DS028471,Krause-Kivlin syndrome
+BMGC_DS07644,BMG_DS028472,Zimmerman Laband syndrome
+BMGC_DS07645,BMG_DS028473,"microphthalmia, syndromic 1"
+BMGC_DS07646,BMG_DS028474,Spastic paraplegia 23
+BMGC_DS07647,BMG_DS028475,Lowry Maclean syndrome
+BMGC_DS07648,BMG_DS028476,Lowry Wood syndrome
+BMGC_DS07649,BMG_DS028477,Lujan Fryns syndrome
+BMGC_DS07650,BMG_DS028478,Lysine Malabsorption Syndrome
+BMGC_DS07651,BMG_DS028479,MacDermot Winter syndrome
+BMGC_DS07652,BMG_DS028480,"ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION"
+BMGC_DS07653,BMG_DS028481,Malouf syndrome
+BMGC_DS07654,BMG_DS028482,Malpuech facial clefting syndrome
+BMGC_DS07655,BMG_DS028483,MARDEN-WALKER SYNDROME
+BMGC_DS07656,BMG_DS028485,Martsolf syndrome
+BMGC_DS07657,BMG_DS028487,Reardon Wilson Cavanagh syndrome
+BMGC_DS07658,BMG_DS028488,Gurrieri Sammito Bellussi syndrome
+BMGC_DS07659,BMG_DS028489,Mercaptolactate-Cysteine Disulfiduria
+BMGC_DS07660,BMG_DS028491,Mexican Cardiomelic Dysplasia
+BMGC_DS07661,BMG_DS028492,Oculopalatoskeletal syndrome
+BMGC_DS07662,BMG_DS028494,Jawad syndrome
+BMGC_DS07663,BMG_DS028495,Microcephaly cervical spine fusion anomalies
+BMGC_DS07664,BMG_DS028496,Oculodigitoesophagoduodenal syndrome
+BMGC_DS07665,BMG_DS028497,"MICROPHTHALMIA, SYNDROMIC 7"
+BMGC_DS07666,BMG_DS028498,Mirhosseini-Holmes-Walton syndrome
+BMGC_DS07667,BMG_DS028499,MOHR-TRANEBJAERG SYNDROME
+BMGC_DS07668,BMG_DS028503,Myhre syndrome
+BMGC_DS07669,BMG_DS028504,Najjar syndrome
+BMGC_DS07670,BMG_DS028505,Nance-Horan syndrome
+BMGC_DS07671,BMG_DS028506,Neuhauser syndrome
+BMGC_DS07672,BMG_DS028508,"LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE"
+BMGC_DS07673,BMG_DS028509,Oculocerebrocutaneous syndrome
+BMGC_DS07674,BMG_DS028510,Odontoonychodermal dysplasia
+BMGC_DS07675,BMG_DS028511,Blepharophimosis syndrome Ohdo type
+BMGC_DS07676,BMG_DS028512,Opitz trigonocephaly syndrome
+BMGC_DS07677,BMG_DS028513,CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY
+BMGC_DS07678,BMG_DS028514,Orofaciodigital Syndrome VII
+BMGC_DS07679,BMG_DS028515,Orofaciodigital syndrome 8
+BMGC_DS07680,BMG_DS028516,Orofaciodigital syndrome 9
+BMGC_DS07681,BMG_DS028518,"Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor"
+BMGC_DS07682,BMG_DS028519,Pitt-Rogers-Danks Syndrome
+BMGC_DS07683,BMG_DS028522,Primrose syndrome
+BMGC_DS07684,BMG_DS028523,Cataract ataxia deafness
+BMGC_DS07685,BMG_DS028524,Proud Syndrome
+BMGC_DS07686,BMG_DS028525,Absent Eyebrows and Eyelashes with Mental Retardation
+BMGC_DS07687,BMG_DS028526,AICARDI-GOUTIERES SYNDROME 1
+BMGC_DS07688,BMG_DS028527,Ramon Syndrome
+BMGC_DS07689,BMG_DS028528,Renpenning syndrome 1
+BMGC_DS07690,BMG_DS028530,3C syndrome
+BMGC_DS07691,BMG_DS028532,Oculodental syndrome Rutherfurd syndrome
+BMGC_DS07692,BMG_DS028533,Sao Paulo MCA-MR Syndrome
+BMGC_DS07693,BMG_DS028534,Acrocallosal Syndrome
+BMGC_DS07694,BMG_DS028535,Scott Syndrome
+BMGC_DS07695,BMG_DS028536,"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1"
+BMGC_DS07696,BMG_DS028538,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE"
+BMGC_DS07697,BMG_DS028539,Sonoda syndrome
+BMGC_DS07698,BMG_DS028541,"Spondylometaphyseal Dysplasia, X-Linked"
+BMGC_DS07699,BMG_DS028542,Spondyloperipheral dysplasia short ulna
+BMGC_DS07700,BMG_DS028543,Stuve-Wiedemann syndrome
+BMGC_DS07701,BMG_DS028544,Teebi syndrome
+BMGC_DS07702,BMG_DS028545,Acromelic frontonasal dysplasia
+BMGC_DS07703,BMG_DS028546,"Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence"
+BMGC_DS07704,BMG_DS028548,Van Den Bosch Syndrome
+BMGC_DS07705,BMG_DS028549,Waisman syndrome
+BMGC_DS07706,BMG_DS028550,Pashayan syndrome
+BMGC_DS07707,BMG_DS028552,Wieacker-Wolff syndrome
+BMGC_DS07708,BMG_DS028554,WOODS SYNDROME
+BMGC_DS07709,BMG_DS028555,Worster Drought syndrome
+BMGC_DS07710,BMG_DS028556,"SPINOCEREBELLAR ATAXIA, X-LINKED 1"
+BMGC_DS07711,BMG_DS028558,"intellectual disability, X-linked 2"
+BMGC_DS07712,BMG_DS028559,"METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblX TYPE"
+BMGC_DS07713,BMG_DS028560,"intellectual disability, X-linked 9"
+BMGC_DS07714,BMG_DS028561,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 12"
+BMGC_DS07715,BMG_DS028562,"intellectual disability, X-linked 14"
+BMGC_DS07716,BMG_DS028563,RAYNAUD-CLAES SYNDROME
+BMGC_DS07717,BMG_DS028564,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 13"
+BMGC_DS07718,BMG_DS028565,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 19"
+BMGC_DS07719,BMG_DS028566,"intellectual disability, X-linked 20"
+BMGC_DS07720,BMG_DS028567,"intellectual disability, X-linked 23"
+BMGC_DS07721,BMG_DS028568,Bohring syndrome
+BMGC_DS07722,BMG_DS028569,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 30"
+BMGC_DS07723,BMG_DS028570,CHROMOSOME Xp11.22 DUPLICATION SYNDROME
+BMGC_DS07724,BMG_DS028571,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 29"
+BMGC_DS07725,BMG_DS028572,Partington syndrome
+BMGC_DS07726,BMG_DS028573,Pettigrew syndrome
+BMGC_DS07727,BMG_DS028575,Sabinas brittle hair syndrome
+BMGC_DS07728,BMG_DS028576,Brown-Vialetto-van Laere syndrome 1
+BMGC_DS07729,BMG_DS028577,Brunner Syndrome
+BMGC_DS07730,BMG_DS028579,Carnevale syndrome
+BMGC_DS07731,BMG_DS028580,Acromegaloid facial appearance syndrome
+BMGC_DS07732,BMG_DS028581,CAHMR syndrome
+BMGC_DS07733,BMG_DS028584,adult choroid plexus neoplasm
+BMGC_DS07734,BMG_DS028586,Ewing sarcoma
+BMGC_DS07735,BMG_DS028587,childhood testicular germ cell tumor
+BMGC_DS07736,BMG_DS028588,pediatric ovarian germ cell tumor
+BMGC_DS07737,BMG_DS028590,Branchio-skeleto-genital syndrome
+BMGC_DS07738,BMG_DS028594,malignant pleural mesothelioma
+BMGC_DS07739,BMG_DS028595,oculodentodigital dysplasia
+BMGC_DS07740,BMG_DS028596,Ulnar Nerve Palsy
+BMGC_DS07741,BMG_DS028598,Circadian Rhythm Disorders
+BMGC_DS07742,BMG_DS028599,hypertriglyceridemia
+BMGC_DS07743,BMG_DS028601,Alcohol Related Neurodevelopmental Disorder
+BMGC_DS07744,BMG_DS028603,Thrombocytosis
+BMGC_DS07745,BMG_DS028621,Spastic quadriplegic cerebral palsy
+BMGC_DS07746,BMG_DS029146,Rupture of bladder
+BMGC_DS07747,BMG_DS029148,acanthoma
+BMGC_DS07748,BMG_DS029156,hypospadias
+BMGC_DS07749,BMG_DS029157,eye carcinoma
+BMGC_DS07750,BMG_DS029158,trachea carcinoma
+BMGC_DS07751,BMG_DS029166,Infection caused by Helicobacter pylori
+BMGC_DS07752,BMG_DS029172,uterine cervix carcinoma in situ
+BMGC_DS07753,BMG_DS029189,Pneumocystis Infections
+BMGC_DS07754,BMG_DS029191,"hypertension, pregnancy-induced"
+BMGC_DS07755,BMG_DS029192,"Blood Coagulation Disorders, Inherited"
+BMGC_DS07756,BMG_DS029195,Respiratory Distress Syndrome
+BMGC_DS07757,BMG_DS029199,Moraxella Infections
+BMGC_DS07758,BMG_DS029202,endobronchial lipoma
+BMGC_DS07759,BMG_DS029209,penile carcinoma
+BMGC_DS07760,BMG_DS029210,bipolar I disorder
+BMGC_DS07761,BMG_DS029211,viral laryngitis
+BMGC_DS07762,BMG_DS029214,retinal melanoma
+BMGC_DS07763,BMG_DS029215,renal pelvis papillary tumor
+BMGC_DS07764,BMG_DS029218,neutropenia
+BMGC_DS07765,BMG_DS029219,breast hemangioma
+BMGC_DS07766,BMG_DS029222,invasive breast carcinoma
+BMGC_DS07767,BMG_DS029223,Diabetic Cardiomyopathies
+BMGC_DS07768,BMG_DS029225,Insulin-resistant diabetes mellitus
+BMGC_DS07769,BMG_DS029226,Ruptured Appendicitis
+BMGC_DS07770,BMG_DS029230,Feeding Disorders
+BMGC_DS07771,BMG_DS029231,Papillary conjunctivitis
+BMGC_DS07772,BMG_DS029232,hepatobiliary neoplasm
+BMGC_DS07773,BMG_DS029233,Bacterial keratitis
+BMGC_DS07774,BMG_DS029235,Bacterial meningitis caused by Gram-negative bacteria
+BMGC_DS07775,BMG_DS029237,Pneumonia caused by Gram negative bacteria
+BMGC_DS07776,BMG_DS029238,Infection caused by anaerobic bacteria
+BMGC_DS07777,BMG_DS029240,herpes simplex dermatitis
+BMGC_DS07778,BMG_DS029245,functioning pituitary gland adenoma
+BMGC_DS07779,BMG_DS029253,trichomegaly
+BMGC_DS07780,BMG_DS029255,Retinal Dystrophies
+BMGC_DS07781,BMG_DS029256,liver cancer
+BMGC_DS07782,BMG_DS029257,refractory precursor T-lymphoblastic lymphoma/leukemia
+BMGC_DS07783,BMG_DS029258,pericardial mesothelioma
+BMGC_DS07784,BMG_DS029259,peritoneal mesothelioma
+BMGC_DS07785,BMG_DS029260,angiosarcoma
+BMGC_DS07786,BMG_DS029261,pineal region germinoma
+BMGC_DS07787,BMG_DS029262,bilateral retinoblastoma
+BMGC_DS07788,BMG_DS029263,unilateral retinoblastoma
+BMGC_DS07789,BMG_DS029264,rhabdoid tumor of the kidney
+BMGC_DS07790,BMG_DS029265,regional ureteric cancer
+BMGC_DS07791,BMG_DS029266,endometrial serous adenocarcinoma
+BMGC_DS07792,BMG_DS029267,paranasal sinus carcinoma
+BMGC_DS07793,BMG_DS029268,peripheral primitive neuroectodermal tumor of bone
+BMGC_DS07794,BMG_DS029269,localized chondrosarcoma
+BMGC_DS07795,BMG_DS029270,extraosseous osteosarcoma
+BMGC_DS07796,BMG_DS029272,relapsed/refractory diffuse large B-cell lymphoma
+BMGC_DS07797,BMG_DS029274,embryonal carcinoma
+BMGC_DS07798,BMG_DS029275,immature extragonadal teratoma
+BMGC_DS07799,BMG_DS029276,placental choriocarcinoma
+BMGC_DS07800,BMG_DS029277,malignant testicular germ cell tumor
+BMGC_DS07801,BMG_DS029286,Acute exacerbation of chronic bronchitis
+BMGC_DS07802,BMG_DS029288,Aneurysm of descending aorta
+BMGC_DS07803,BMG_DS029290,Budd-Chiari Syndrome
+BMGC_DS07804,BMG_DS029293,dehydration polycythemia
+BMGC_DS07805,BMG_DS029294,physiological polycythemia
+BMGC_DS07806,BMG_DS029295,polycythemia due to hypoxia
+BMGC_DS07807,BMG_DS029296,acute graft versus host disease
+BMGC_DS07808,BMG_DS029297,Chondrocalcinosis 2
+BMGC_DS07809,BMG_DS029299,acquired hemangioma
+BMGC_DS07810,BMG_DS029300,skin sarcoma
+BMGC_DS07811,BMG_DS029301,Retinol Deficiency
+BMGC_DS07812,BMG_DS029304,"Hyperbilirubinemia, Neonatal"
+BMGC_DS07813,BMG_DS029314,Staphylococcus Aureus Pneumonia
+BMGC_DS07814,BMG_DS029316,breast adenocarcinoma
+BMGC_DS07815,BMG_DS029317,early-onset posterior polar cataract
+BMGC_DS07816,BMG_DS029318,Dyschromatopsia
+BMGC_DS07817,BMG_DS029319,"Blindness, Cortical, Transient"
+BMGC_DS07818,BMG_DS029323,diffuse glomerulonephritis
+BMGC_DS07819,BMG_DS029327,hair follicle neoplasm
+BMGC_DS07820,BMG_DS029329,transient hypogammaglobulinemia
+BMGC_DS07821,BMG_DS029330,Idiopathic achalasia of esophagus
+BMGC_DS07822,BMG_DS029331,Vaginal Yeast Infections
+BMGC_DS07823,BMG_DS029333,Leydig cell hypoplasia
+BMGC_DS07824,BMG_DS029336,Cholestatic liver disease
+BMGC_DS07825,BMG_DS029337,Drug-Induced Liver Disease
+BMGC_DS07826,BMG_DS029339,"Hernia, Double Inguinal"
+BMGC_DS07827,BMG_DS029342,Retinoic acid syndrome
+BMGC_DS07828,BMG_DS029343,medullary breast carcinoma
+BMGC_DS07829,BMG_DS029348,lobular neoplasia
+BMGC_DS07830,BMG_DS029349,adenosquamous bile duct carcinoma
+BMGC_DS07831,BMG_DS029350,extrahepatic bile duct clear cell adenocarcinoma
+BMGC_DS07832,BMG_DS029351,extrahepatic bile duct mucinous adenocarcinoma
+BMGC_DS07833,BMG_DS029352,papillary extrahepatic bile duct adenocarcinoma
+BMGC_DS07834,BMG_DS029353,extrahepatic bile duct signet ring cell carcinoma
+BMGC_DS07835,BMG_DS029354,squamous cell bile duct carcinoma
+BMGC_DS07836,BMG_DS029355,B-lymphoblastic leukemia/lymphoma
+BMGC_DS07837,BMG_DS029357,malignant epithelioid mesothelioma
+BMGC_DS07838,BMG_DS029359,urethra transitional cell carcinoma
+BMGC_DS07839,BMG_DS029360,rete testis adenocarcinoma
+BMGC_DS07840,BMG_DS029361,testicular Leydig cell tumor
+BMGC_DS07841,BMG_DS029362,Ewing sarcoma
+BMGC_DS07842,BMG_DS029386,Polycythemia due to fall in plasma volume
+BMGC_DS07843,BMG_DS029389,Idiopathic Parkinsonism or Parkinson's disease
+BMGC_DS07844,BMG_DS029390,Primary Parkinsonism or Parkinson's disease
+BMGC_DS07845,BMG_DS029402,diffuse pulmonary fibrosis
+BMGC_DS07846,BMG_DS029415,Chronic graft-versus-host disease
+BMGC_DS07847,BMG_DS029420,Late neonatal hypocalcemia
+BMGC_DS07848,BMG_DS029425,Carditis
+BMGC_DS07849,BMG_DS029429,Hyperkeratosis
+BMGC_DS07850,BMG_DS029433,Sarcopenia
+BMGC_DS07851,BMG_DS029434,mitochondrial neurogastrointestinal encephalomyopathy
+BMGC_DS07852,BMG_DS029440,Schimke immuno-osseous dysplasia
+BMGC_DS07853,BMG_DS029449,Patellofemoral Pain Syndrome
+BMGC_DS07854,BMG_DS029450,necrotizing gastritis
+BMGC_DS07855,BMG_DS029454,Peripartum cardiomyopathy
+BMGC_DS07856,BMG_DS029460,thyroid malformation
+BMGC_DS07857,BMG_DS029461,cerebral hemangioma
+BMGC_DS07858,BMG_DS029464,Exostoses Of Heel
+BMGC_DS07859,BMG_DS029466,Candidemia
+BMGC_DS07860,BMG_DS029469,ovarian serous cystadenofibroma
+BMGC_DS07861,BMG_DS029470,cervix melanoma
+BMGC_DS07862,BMG_DS029473,Askin tumor
+BMGC_DS07863,BMG_DS029474,Cerebral Arteriosclerosis
+BMGC_DS07864,BMG_DS029475,Cerebral Embolism and Thrombosis
+BMGC_DS07865,BMG_DS029476,aleukemic leukemia
+BMGC_DS07866,BMG_DS029478,Arteriolosclerosis
+BMGC_DS07867,BMG_DS029483,Cardiomyopathies
+BMGC_DS07868,BMG_DS029484,Diffuse panbronchiolitis
+BMGC_DS07869,BMG_DS029486,Posterior Leukoencephalopathy Syndrome
+BMGC_DS07870,BMG_DS029488,"acetylation, slow"
+BMGC_DS07871,BMG_DS029489,Sphincter of Oddi Dysfunction
+BMGC_DS07872,BMG_DS029492,Erdheim-Chester Disease
+BMGC_DS07873,BMG_DS029493,6-pyruvoyl-tetrahydropterin synthase deficiency
+BMGC_DS07874,BMG_DS029494,Glycogen Storage Disease Type IIb
+BMGC_DS07875,BMG_DS029495,Dent's disease
+BMGC_DS07876,BMG_DS029496,Deficiency of ferroxidase (disorder)
+BMGC_DS07877,BMG_DS029497,"pituitary hormone deficiency, combined, 2"
+BMGC_DS07878,BMG_DS029498,SHORT syndrome
+BMGC_DS07879,BMG_DS029499,Conjunctivochalasis
+BMGC_DS07880,BMG_DS029503,Synovial Plica Syndrome
+BMGC_DS07881,BMG_DS029504,Overactive Bladder
+BMGC_DS07882,BMG_DS029506,hereditary papillary renal cell carcinoma
+BMGC_DS07883,BMG_DS029507,hereditary kidney oncocytoma
+BMGC_DS07884,BMG_DS029508,Posterior Choroidal Artery Infarction
+BMGC_DS07885,BMG_DS029510,pancreatic ductal carcinoma
+BMGC_DS07886,BMG_DS029511,aleukemic leukemia cutis
+BMGC_DS07887,BMG_DS029512,"Polycystic Kidney, Type 1 Autosomal Dominant Disease"
+BMGC_DS07888,BMG_DS029516,Becker Muscular Dystrophy
+BMGC_DS07889,BMG_DS029517,Hajdu-Cheney Syndrome
+BMGC_DS07890,BMG_DS029518,Pulmonic Plague
+BMGC_DS07891,BMG_DS029519,"Optic Atrophy, Hereditary, Leber"
+BMGC_DS07892,BMG_DS029520,brain ischemia
+BMGC_DS07893,BMG_DS029521,Hypersomnia
+BMGC_DS07894,BMG_DS029522,"Epilepsy, Myoclonic, Infantile"
+BMGC_DS07895,BMG_DS029523,insomnia
+BMGC_DS07896,BMG_DS029524,arteriovenous malformations of the brain
+BMGC_DS07897,BMG_DS029525,Transient Cerebral Ischemia
+BMGC_DS07898,BMG_DS029526,Haemophilus influenzae Meningitis Type B
+BMGC_DS07899,BMG_DS029528,Nerve Entrapment
+BMGC_DS07900,BMG_DS029529,Tetanilla
+BMGC_DS07901,BMG_DS029531,esophageal diverticulosis
+BMGC_DS07902,BMG_DS029534,Progressive Muscular Atrophy
+BMGC_DS07903,BMG_DS029535,Acro-Osteolysis
+BMGC_DS07904,BMG_DS029536,Cerebral Aneurysm
+BMGC_DS07905,BMG_DS029537,ovarian neoplasm
+BMGC_DS07906,BMG_DS029538,Decreased Intraocular Pressure-Associated Papilledema
+BMGC_DS07907,BMG_DS029542,"Upper Extremity Deep Vein Thrombosis, Primary"
+BMGC_DS07908,BMG_DS029543,postauricular lymphadenitis
+BMGC_DS07909,BMG_DS029548,Cytokine Storm
+BMGC_DS07910,BMG_DS029549,axillary lymphadenitis
+BMGC_DS07911,BMG_DS029560,eyelid carcinoma
+BMGC_DS07912,BMG_DS029562,small intestine leiomyosarcoma
+BMGC_DS07913,BMG_DS029564,"spondyloepimetaphyseal dysplasia, Sponastrime type"
+BMGC_DS07914,BMG_DS029565,Autoimmune thyroiditis
+BMGC_DS07915,BMG_DS029569,Testicular Feminization
+BMGC_DS07916,BMG_DS029570,Vitamin B 6 Deficiency
+BMGC_DS07917,BMG_DS029572,HIV-1-Associated Cognitive Motor Complex
+BMGC_DS07918,BMG_DS029574,Brain Embolism and Thrombosis
+BMGC_DS07919,BMG_DS029575,chondroma
+BMGC_DS07920,BMG_DS029576,Eczema Herpeticum
+BMGC_DS07921,BMG_DS029577,Polyradiculitis
+BMGC_DS07922,BMG_DS029579,Lysine Alpha-Ketoglutarate Reductase Deficiency Disease
+BMGC_DS07923,BMG_DS029581,Brain Thrombus
+BMGC_DS07924,BMG_DS029582,Cerebral Thrombus
+BMGC_DS07925,BMG_DS029583,"Familial Amyloid Polyneuropathy, Type IV"
+BMGC_DS07926,BMG_DS029584,blastoma
+BMGC_DS07927,BMG_DS029585,lipoma of colon
+BMGC_DS07928,BMG_DS029593,Cholecystolithiasis
+BMGC_DS07929,BMG_DS029596,Ischemic stroke
+BMGC_DS07930,BMG_DS029597,Gastritis caused by bacterium
+BMGC_DS07931,BMG_DS029601,Acute Coronary Syndrome
+BMGC_DS07932,BMG_DS029605,Tracheomalacia
+BMGC_DS07933,BMG_DS029607,Infection caused by Citrobacter
+BMGC_DS07934,BMG_DS029609,ovarian adenocarcinoma
+BMGC_DS07935,BMG_DS029611,Cytokine Release Syndrome
+BMGC_DS07936,BMG_DS029614,Hemodynamic instability
+BMGC_DS07937,BMG_DS029621,McKusick-Kaufman syndrome
+BMGC_DS07938,BMG_DS029629,Coronary Restenosis
+BMGC_DS07939,BMG_DS029635,Gastritis caused by fungus
+BMGC_DS07940,BMG_DS029638,pituitary hypoplasia
+BMGC_DS07941,BMG_DS029639,retroperitoneum carcinoma
+BMGC_DS07942,BMG_DS029640,salivary gland carcinoma
+BMGC_DS07943,BMG_DS029643,Gastrointestinal hypomotility
+BMGC_DS07944,BMG_DS029646,Primary hypogonadism
+BMGC_DS07945,BMG_DS029648,intraductal breast neoplasm
+BMGC_DS07946,BMG_DS029649,rectal cancer
+BMGC_DS07947,BMG_DS029651,polyp of large intestine
+BMGC_DS07948,BMG_DS029652,Hospital acquired pneumonia
+BMGC_DS07949,BMG_DS029653,Congenital hypoplastic anemia
+BMGC_DS07950,BMG_DS029654,Acute laryngitis with obstruction
+BMGC_DS07951,BMG_DS029664,Ileocolitis
+BMGC_DS07952,BMG_DS029665,gonadal agenesis
+BMGC_DS07953,BMG_DS029666,Neonatal Diseases and Abnormalities
+BMGC_DS07954,BMG_DS029667,Luft Disease
+BMGC_DS07955,BMG_DS029669,Porokeratosis of Mibelli
+BMGC_DS07956,BMG_DS029670,wheat allergy
+BMGC_DS07957,BMG_DS029671,ovarian dysgenesis 1
+BMGC_DS07958,BMG_DS029673,"Cardiomyopathy, Hypertrophic, Familial"
+BMGC_DS07959,BMG_DS029674,Tauopathies
+BMGC_DS07960,BMG_DS029676,Spondylarthritis
+BMGC_DS07961,BMG_DS029677,Spondylarthropathies
+BMGC_DS07962,BMG_DS029678,Polyomavirus Infections
+BMGC_DS07963,BMG_DS029679,"Electron Transport Chain Deficiencies, Mitochondrial"
+BMGC_DS07964,BMG_DS029680,Oxidative Phosphorylation Deficiencies
+BMGC_DS07965,BMG_DS029681,Mitochondrial Respiratory Chain Deficiencies
+BMGC_DS07966,BMG_DS029684,Denys-Drash Syndrome
+BMGC_DS07967,BMG_DS029685,Frasier Syndrome
+BMGC_DS07968,BMG_DS029686,"Genetic Diseases, Inborn"
+BMGC_DS07969,BMG_DS029687,Disease due to Papilloma virus
+BMGC_DS07970,BMG_DS029688,Autosomal Chromosome Disorders
+BMGC_DS07971,BMG_DS029690,Dysphasia
+BMGC_DS07972,BMG_DS029692,Type 1 Duane Retraction Syndrome
+BMGC_DS07973,BMG_DS029694,Drug Resistant Epilepsy
+BMGC_DS07974,BMG_DS029701,Kinsbourne Syndrome
+BMGC_DS07975,BMG_DS029702,Macrophage Activation Syndrome
+BMGC_DS07976,BMG_DS029712,pancreas sarcoma
+BMGC_DS07977,BMG_DS029713,neurofibroma of the heart
+BMGC_DS07978,BMG_DS029720,Peptostreptococcus infection
+BMGC_DS07979,BMG_DS029725,ovarian cystadenocarcinoma
+BMGC_DS07980,BMG_DS029726,appendix mucinous cystadenocarcinoma
+BMGC_DS07981,BMG_DS029731,Infantile Sialic Acid Storage Disease
+BMGC_DS07982,BMG_DS029732,Salla disease
+BMGC_DS07983,BMG_DS029733,nipple neoplasm
+BMGC_DS07984,BMG_DS029736,Sensorimotor neuropathy
+BMGC_DS07985,BMG_DS029739,epiglottis cancer
+BMGC_DS07986,BMG_DS029741,peripheral primitive neuroectodermal tumor of soft tissues
+BMGC_DS07987,BMG_DS029744,esophageal small cell neuroendocrine carcinoma
+BMGC_DS07988,BMG_DS029745,aggressive systemic mastocytosis
+BMGC_DS07989,BMG_DS029747,oral mucosa leukoplakia
+BMGC_DS07990,BMG_DS029748,paraneoplastic pemphigus
+BMGC_DS07991,BMG_DS029750,Granulomatous gastritis
+BMGC_DS07992,BMG_DS029755,liver lymphoma
+BMGC_DS07993,BMG_DS029756,sickle cell-hemoglobin E disease syndrome
+BMGC_DS07994,BMG_DS029758,childhood spinal cord tumor
+BMGC_DS07995,BMG_DS029759,invasive ductal carcinoma
+BMGC_DS07996,BMG_DS029761,aqueous misdirection
+BMGC_DS07997,BMG_DS029762,"Heart Failure, Systolic"
+BMGC_DS07998,BMG_DS029764,"Heart Failure, Diastolic"
+BMGC_DS07999,BMG_DS029768,Dieulafoy lesion (hemorrhagic) of stomach and duodenum
+BMGC_DS08000,BMG_DS029779,"Meningitis, Meningococcal, Serogroup A"
+BMGC_DS08001,BMG_DS029780,"Meningitis, Meningococcal, Serogroup B"
+BMGC_DS08002,BMG_DS029781,"Meningitis, Meningococcal, Serogroup C"
+BMGC_DS08003,BMG_DS029782,"Acquired Metabolic Diseases, Nervous System"
+BMGC_DS08004,BMG_DS029785,gestational trophoblastic neoplasm
+BMGC_DS08005,BMG_DS029787,non-gestational choriocarcinoma
+BMGC_DS08006,BMG_DS029788,"Wasting Disease, Chronic"
+BMGC_DS08007,BMG_DS029789,cutaneous mastocytosis
+BMGC_DS08008,BMG_DS029790,Plasma cell dyscrasia
+BMGC_DS08009,BMG_DS029792,Water Stress
+BMGC_DS08010,BMG_DS029795,"Meningitis, Meningococcal, Serogroup Y"
+BMGC_DS08011,BMG_DS029796,"Meningitis, Meningococcal, Serogroup W-135"
+BMGC_DS08012,BMG_DS029797,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED"
+BMGC_DS08013,BMG_DS029798,HIV-Associated Lipodystrophy Syndrome
+BMGC_DS08014,BMG_DS029800,Sclerocystic Ovaries
+BMGC_DS08015,BMG_DS029801,"Retinoschisis, Degenerative"
+BMGC_DS08016,BMG_DS029803,"Genetic Diseases, X-Linked"
+BMGC_DS08017,BMG_DS029804,ovarian cancer
+BMGC_DS08018,BMG_DS029805,Familial long QT syndrome
+BMGC_DS08019,BMG_DS029806,Purple glove syndrome
+BMGC_DS08020,BMG_DS029811,Carnitine deficiency
+BMGC_DS08021,BMG_DS029813,Brugada syndrome
+BMGC_DS08022,BMG_DS029823,Bacteremia caused by Staphylococcus aureus
+BMGC_DS08023,BMG_DS029830,autonomic nervous system disorder
+BMGC_DS08024,BMG_DS029831,Respiratory Failure
+BMGC_DS08025,BMG_DS029832,Stomach Diverticulosis
+BMGC_DS08026,BMG_DS029833,X-Linked Dyskeratosis Congenita
+BMGC_DS08027,BMG_DS029834,endometrium adenocarcinoma
+BMGC_DS08028,BMG_DS029835,chronic polyneuropathy
+BMGC_DS08029,BMG_DS029838,Pleuropericarditis
+BMGC_DS08030,BMG_DS029840,Cogan-Reese syndrome
+BMGC_DS08031,BMG_DS029842,recurrent respiratory papillomatosis
+BMGC_DS08032,BMG_DS029843,infectious otitis interna
+BMGC_DS08033,BMG_DS029847,head and neck squamous cell carcinoma
+BMGC_DS08034,BMG_DS029850,Severe Acute Respiratory Syndrome
+BMGC_DS08035,BMG_DS029851,breast ductal carcinoma
+BMGC_DS08036,BMG_DS029853,Child Malnutrition
+BMGC_DS08037,BMG_DS029854,Overnutrition
+BMGC_DS08038,BMG_DS029855,Child Overnutrition
+BMGC_DS08039,BMG_DS029856,Infant Overnutrition
+BMGC_DS08040,BMG_DS029857,"Steroid Metabolism, Inborn Errors"
+BMGC_DS08041,BMG_DS029858,Clostridium difficile colitis
+BMGC_DS08042,BMG_DS029859,Clostridium Enterocolitis
+BMGC_DS08043,BMG_DS029860,"Enteritis, Pseudomembranous"
+BMGC_DS08044,BMG_DS029867,extra-adrenal sympathetic paraganglioma
+BMGC_DS08045,BMG_DS029869,Intestinal Polyposis
+BMGC_DS08046,BMG_DS029870,Glucose Metabolism Disorders
+BMGC_DS08047,BMG_DS029872,Endogenous Hyperinsulinism
+BMGC_DS08048,BMG_DS029873,Exogenous Hyperinsulinism
+BMGC_DS08049,BMG_DS029874,Compensatory Hyperinsulinemia
+BMGC_DS08050,BMG_DS029878,Barrett Epithelium
+BMGC_DS08051,BMG_DS029880,Diffuse Scleroderma
+BMGC_DS08052,BMG_DS029881,Ileus
+BMGC_DS08053,BMG_DS029889,Moraxellaceae Infections
+BMGC_DS08054,BMG_DS029890,Psychobacter Infections
+BMGC_DS08055,BMG_DS029891,follicular dendritic cell sarcoma
+BMGC_DS08056,BMG_DS029892,interdigitating dendritic cell sarcoma
+BMGC_DS08057,BMG_DS029893,Langerhans cell sarcoma
+BMGC_DS08058,BMG_DS029898,splenic sequestration
+BMGC_DS08059,BMG_DS029899,myasthenia gravis
+BMGC_DS08060,BMG_DS029905,Aortic valve disorder
+BMGC_DS08061,BMG_DS029920,"Anemia, Diamond-Blackfan"
+BMGC_DS08062,BMG_DS029923,Dysfibrinogenemia
+BMGC_DS08063,BMG_DS029925,Infection by Pasteurella multocida
+BMGC_DS08064,BMG_DS029928,Late latent syphilis
+BMGC_DS08065,BMG_DS029929,Proteus pneumonia
+BMGC_DS08066,BMG_DS029934,ductal eccrine adenocarcinoma
+BMGC_DS08067,BMG_DS029935,lipoblastoma
+BMGC_DS08068,BMG_DS029941,Progeria short stature pigmented nevi
+BMGC_DS08069,BMG_DS029945,Pontoneocerebellar hypoplasia
+BMGC_DS08070,BMG_DS029949,Pelvic inflammatory disease caused by Metamycoplasma hominis
+BMGC_DS08071,BMG_DS029952,Trigonitis
+BMGC_DS08072,BMG_DS029954,Actinomycetoma
+BMGC_DS08073,BMG_DS029956,"Degeneration of macula due to cyst, hole or pseudohole"
+BMGC_DS08074,BMG_DS029964,sarcoma
+BMGC_DS08075,BMG_DS029967,Bacterial sinusitis
+BMGC_DS08076,BMG_DS029970,Fungal keratitis
+BMGC_DS08077,BMG_DS029977,Eosinophilic gastroenteritis
+BMGC_DS08078,BMG_DS029982,"Hepatitis, Drug-Induced"
+BMGC_DS08079,BMG_DS030019,Subacute glomerulonephritis
+BMGC_DS08080,BMG_DS030030,Female genital tract infection
+BMGC_DS08081,BMG_DS030051,attention deficit-hyperactivity disorder
+BMGC_DS08082,BMG_DS030060,Peripheral axonal neuropathy
+BMGC_DS08083,BMG_DS030061,"Muscular dystrophy congenital, merosin negative"
+BMGC_DS08084,BMG_DS030079,neoplasm of cerebral hemisphere
+BMGC_DS08085,BMG_DS030080,frontal lobe neoplasm
+BMGC_DS08086,BMG_DS030081,neoplasm of temporal lobe
+BMGC_DS08087,BMG_DS030082,neoplasm of parietal lobe
+BMGC_DS08088,BMG_DS030083,occipital lobe neoplasm
+BMGC_DS08089,BMG_DS030084,cauda equina neoplasm
+BMGC_DS08090,BMG_DS030085,oculomotor nerve neoplasm
+BMGC_DS08091,BMG_DS030086,trochlear nerve neoplasm
+BMGC_DS08092,BMG_DS030087,trigeminal nerve neoplasm
+BMGC_DS08093,BMG_DS030088,abducens nerve neoplasm
+BMGC_DS08094,BMG_DS030089,facial nerve neoplasm
+BMGC_DS08095,BMG_DS030090,glossopharyngeal nerve neoplasm
+BMGC_DS08096,BMG_DS030091,vagus nerve neoplasm
+BMGC_DS08097,BMG_DS030092,spinal accessory nerve neoplasm
+BMGC_DS08098,BMG_DS030093,hypoglossal nerve neoplasm
+BMGC_DS08099,BMG_DS030125,Sickle cell-Hemoglobin O Arab disease
+BMGC_DS08100,BMG_DS030155,"von Willebrand Disease, Type 1"
+BMGC_DS08101,BMG_DS030156,"von Willebrand Disease, Type 2"
+BMGC_DS08102,BMG_DS030157,"von Willebrand Disease, Type 3"
+BMGC_DS08103,BMG_DS030204,large cell neuroendocrine carcinoma
+BMGC_DS08104,BMG_DS030205,large cell carcinoma with rhabdoid phenotype
+BMGC_DS08105,BMG_DS030206,basaloid squamous cell carcinoma
+BMGC_DS08106,BMG_DS030207,non-invasive bladder papillary urothelial neoplasm
+BMGC_DS08107,BMG_DS030208,sclerosing hepatic carcinoma
+BMGC_DS08108,BMG_DS030209,hepatocellular clear cell carcinoma
+BMGC_DS08109,BMG_DS030210,pregnancy adenoma
+BMGC_DS08110,BMG_DS030211,anal gland adenocarcinoma
+BMGC_DS08111,BMG_DS030215,biliary papillomatosis
+BMGC_DS08112,BMG_DS030216,chromophobe renal cell carcinoma
+BMGC_DS08113,BMG_DS030217,sarcomatoid renal cell carcinoma
+BMGC_DS08114,BMG_DS030218,collecting duct carcinoma
+BMGC_DS08115,BMG_DS030219,metanephric adenoma
+BMGC_DS08116,BMG_DS030220,thyroid gland atypical follicular adenoma
+BMGC_DS08117,BMG_DS030222,secretory uterine corpus endometrioid adenocarcinoma
+BMGC_DS08118,BMG_DS030224,malignant spiradenoma
+BMGC_DS08119,BMG_DS030225,eccrine porocarcinoma
+BMGC_DS08120,BMG_DS030226,eccrine adenocarcinoma
+BMGC_DS08121,BMG_DS030227,pancreatic intraductal papillary-mucinous neoplasm
+BMGC_DS08122,BMG_DS030228,pancreatic non-invasive mucinous cystadenocarcinoma
+BMGC_DS08123,BMG_DS030229,endocervical type cervical mucinous adenocarcinoma
+BMGC_DS08124,BMG_DS030230,pancreatic acinar cell cystadenocarcinoma
+BMGC_DS08125,BMG_DS030232,thymoma type A
+BMGC_DS08126,BMG_DS030233,thymoma type AB
+BMGC_DS08127,BMG_DS030234,malignant type AB thymoma
+BMGC_DS08128,BMG_DS030235,thymoma type B1
+BMGC_DS08129,BMG_DS030236,cortical thymoma
+BMGC_DS08130,BMG_DS030238,thymic epithelial neoplasm
+BMGC_DS08131,BMG_DS030239,malignant glomus tumor
+BMGC_DS08132,BMG_DS030240,diffuse meningeal melanocytosis
+BMGC_DS08133,BMG_DS030242,meningeal melanomatosis
+BMGC_DS08134,BMG_DS030243,solitary fibrous tumor
+BMGC_DS08135,BMG_DS030244,myofibroma
+BMGC_DS08136,BMG_DS030246,"histiocytoma, Angiomatoid fibrous"
+BMGC_DS08137,BMG_DS030247,ossifying fibromyxoid tumor
+BMGC_DS08138,BMG_DS030249,fibroblastic liposarcoma
+BMGC_DS08139,BMG_DS030250,chondroid lipoma
+BMGC_DS08140,BMG_DS030251,spindle cell rhabdomyosarcoma
+BMGC_DS08141,BMG_DS030254,nephrogenic adenofibroma
+BMGC_DS08142,BMG_DS030255,pleuropulmonary blastoma
+BMGC_DS08143,BMG_DS030257,epithelioid trophoblastic tumor
+BMGC_DS08144,BMG_DS030258,high grade surface osteosarcoma
+BMGC_DS08145,BMG_DS030259,conventional osteosarcoma
+BMGC_DS08146,BMG_DS030260,clear cell chondrosarcoma
+BMGC_DS08147,BMG_DS030261,malignant tenosynovial giant cell tumor
+BMGC_DS08148,BMG_DS030262,chondroid chordoma
+BMGC_DS08149,BMG_DS030263,parachordoma
+BMGC_DS08150,BMG_DS030265,dysembryoplastic neuroepithelial tumor
+BMGC_DS08151,BMG_DS030266,gliofibroma
+BMGC_DS08152,BMG_DS030267,large cell medulloblastoma
+BMGC_DS08153,BMG_DS030268,atypical teratoid rhabdoid tumor
+BMGC_DS08154,BMG_DS030269,malignant perineurioma
+BMGC_DS08155,BMG_DS030270,"Hodgkin's lymphoma, lymphocytic-histiocytic predominance"
+BMGC_DS08156,BMG_DS030289,Congenital Thrombotic Thrombocytopenic Purpura
+BMGC_DS08157,BMG_DS030293,major depressive disorder
+BMGC_DS08158,BMG_DS030317,ectopia pupillae
+BMGC_DS08159,BMG_DS030318,Pigment dispersion syndrome (disorder)
+BMGC_DS08160,BMG_DS030347,tibial adamantinoma
+BMGC_DS08161,BMG_DS030348,Left ventricular diastolic dysfunction
+BMGC_DS08162,BMG_DS030354,Infection due to Penicillium marneffei (disorder)
+BMGC_DS08163,BMG_DS030376,IgA pemphigus
+BMGC_DS08164,BMG_DS030392,Factitious skin disease
+BMGC_DS08165,BMG_DS030404,autosomal recessive congenital ichthyosis
+BMGC_DS08166,BMG_DS030405,punctate palmoplantar keratoderma
+BMGC_DS08167,BMG_DS030413,Chylomicronemia syndrome
+BMGC_DS08168,BMG_DS030417,T-lymphocyte immunodeficiency
+BMGC_DS08169,BMG_DS030474,Recurrent herpes simplex labialis
+BMGC_DS08170,BMG_DS030476,Recurrent genital herpes simplex
+BMGC_DS08171,BMG_DS030506,Streptococcal infection of skin
+BMGC_DS08172,BMG_DS030548,Primary Cutaneous Nocardiosis
+BMGC_DS08173,BMG_DS030613,Onychomycosis of toenails
+BMGC_DS08174,BMG_DS030691,Demodectic blepharitis
+BMGC_DS08175,BMG_DS030774,Central centrifugal cicatricial alopecia
+BMGC_DS08176,BMG_DS030799,Hyperhidrosis Palmaris Et Plantaris
+BMGC_DS08177,BMG_DS030839,Ligneous conjunctivitis
+BMGC_DS08178,BMG_DS030845,hereditary mucoepithelial dysplasia
+BMGC_DS08179,BMG_DS030870,Systemic lupus erythematosus of childhood
+BMGC_DS08180,BMG_DS030923,Drug-Induced Stevens Johnson Syndrome
+BMGC_DS08181,BMG_DS030972,Drug-induced mucositis
+BMGC_DS08182,BMG_DS031016,Acrocephalopolysyndactyly type 2
+BMGC_DS08183,BMG_DS031017,Sakati syndrome
+BMGC_DS08184,BMG_DS031018,Cardio-facio-cutaneous syndrome
+BMGC_DS08185,BMG_DS031020,hereditary neurocutaneous angioma
+BMGC_DS08186,BMG_DS031023,Dykes Markes Harper syndrome
+BMGC_DS08187,BMG_DS031024,"Ichthyosiform erythroderma, corneal involvement, deafness"
+BMGC_DS08188,BMG_DS031038,Autosomal dominant familial wooly hair
+BMGC_DS08189,BMG_DS031046,Dystrophic epidermolysis bullosa inverse type
+BMGC_DS08190,BMG_DS031047,Epidermolysis Bullosa Pruriginosa
+BMGC_DS08191,BMG_DS031049,Autosomal recessive pseudoxanthoma elasticum
+BMGC_DS08192,BMG_DS031051,familial multiple trichoepithelioma
+BMGC_DS08193,BMG_DS031054,TNF receptor-associated periodic fever syndrome (TRAPS)
+BMGC_DS08194,BMG_DS031071,vulval Paget disease
+BMGC_DS08195,BMG_DS031072,cutaneous glomangioma
+BMGC_DS08196,BMG_DS031078,cutaneous undifferentiated pleomorphic sarcoma
+BMGC_DS08197,BMG_DS031080,epithelioid neurofibroma
+BMGC_DS08198,BMG_DS031081,Familial Multiple Lipomatosis
+BMGC_DS08199,BMG_DS031082,spindle cell liposarcoma
+BMGC_DS08200,BMG_DS031084,extraskeletal myxoid chondrosarcoma
+BMGC_DS08201,BMG_DS031085,extraskeletal mesenchymal chondrosarcoma
+BMGC_DS08202,BMG_DS031134,Funisitis (disorder)
+BMGC_DS08203,BMG_DS031135,melanotic medulloblastoma
+BMGC_DS08204,BMG_DS031136,Meibomian gland dysfunction
+BMGC_DS08205,BMG_DS031137,Avellino corneal dystrophy
+BMGC_DS08206,BMG_DS031139,Herpes zoster keratitis
+BMGC_DS08207,BMG_DS031143,Congenital central hypoventilation
+BMGC_DS08208,BMG_DS031160,Pena-Shokeir syndrome type I
+BMGC_DS08209,BMG_DS031175,Impetiginized atopic dermatitis
+BMGC_DS08210,BMG_DS031228,Infection due to Erysipelothrix rhusiopathiae (disorder)
+BMGC_DS08211,BMG_DS031257,Postnatal infection
+BMGC_DS08212,BMG_DS031259,Chlamydial urethritis
+BMGC_DS08213,BMG_DS031262,Westphal disease
+BMGC_DS08214,BMG_DS031290,periodic paralysis (finding)
+BMGC_DS08215,BMG_DS031293,X-Linked Combined Immunodeficiency Diseases
+BMGC_DS08216,BMG_DS031299,Tinea profunda (disorder)
+BMGC_DS08217,BMG_DS031304,acute interstitial pneumonia
+BMGC_DS08218,BMG_DS031310,Lipoatrophy
+BMGC_DS08219,BMG_DS031312,Podoconiosis
+BMGC_DS08220,BMG_DS031319,Jumping Frenchmen of Maine
+BMGC_DS08221,BMG_DS031322,"Von Willebrand disease, platelet type"
+BMGC_DS08222,BMG_DS031411,Ocular Cicatricial Pemphigoid
+BMGC_DS08223,BMG_DS031422,metastasis from malignant tumor of colon
+BMGC_DS08224,BMG_DS031441,Enthesitis
+BMGC_DS08225,BMG_DS031448,"von Willebrand Disease, Type 2A"
+BMGC_DS08226,BMG_DS031449,"von Willebrand Disease, Type 2B"
+BMGC_DS08227,BMG_DS031451,von Willebrand disease type 2M
+BMGC_DS08228,BMG_DS031452,"von Willebrand Disease, Type 2N"
+BMGC_DS08229,BMG_DS031464,Lymphocytic gastritis
+BMGC_DS08230,BMG_DS031474,Butyrylcholinesterase deficiency
+BMGC_DS08231,BMG_DS031494,"Sucrase-isomaltase deficiency, congenital"
+BMGC_DS08232,BMG_DS031527,Degenerative disorder
+BMGC_DS08233,BMG_DS031540,Fetal Nutrition Disorders
+BMGC_DS08234,BMG_DS031543,Fetal ascites
+BMGC_DS08235,BMG_DS031599,Lesion of ulnar nerve
+BMGC_DS08236,BMG_DS031601,Amyloid of familial Mediterranean fever
+BMGC_DS08237,BMG_DS031662,Arthropathy associated with bacterial disease
+BMGC_DS08238,BMG_DS031681,Subacute bursitis
+BMGC_DS08239,BMG_DS031732,sternal neoplasm
+BMGC_DS08240,BMG_DS031751,Nonspecific interstitial pneumonia
+BMGC_DS08241,BMG_DS031753,epiglottis neoplasm
+BMGC_DS08242,BMG_DS031754,lung hilum neoplasm
+BMGC_DS08243,BMG_DS031755,Acute disease of cardiovascular system
+BMGC_DS08244,BMG_DS031760,Structural disorder of heart
+BMGC_DS08245,BMG_DS031775,neoplasm of endocardium
+BMGC_DS08246,BMG_DS031776,neoplasm of myocardium
+BMGC_DS08247,BMG_DS031777,neoplasm of epicardium
+BMGC_DS08248,BMG_DS031778,vascular cancer
+BMGC_DS08249,BMG_DS032021,3-Hydroxyacyl-CoA Dehydrogenase Deficiency
+BMGC_DS08250,BMG_DS032036,Cortisone reductase deficiency
+BMGC_DS08251,BMG_DS032090,Deficiency of iodide peroxidase (disorder)
+BMGC_DS08252,BMG_DS032120,Transaldolase Deficiency
+BMGC_DS08253,BMG_DS032162,Deficiency of sedoheptulokinase
+BMGC_DS08254,BMG_DS032175,D-glycericacidemia
+BMGC_DS08255,BMG_DS032190,Phosphoribosylpyrophosphate synthetase deficiency
+BMGC_DS08256,BMG_DS032249,Deficiency of phosphoserine phosphatase
+BMGC_DS08257,BMG_DS032275,Hyaluronidase Deficiency
+BMGC_DS08258,BMG_DS032297,Beta-Ureidopropionase Deficiency
+BMGC_DS08259,BMG_DS032344,Deficiency of phosphoribosylaminoimidazole carboxylase
+BMGC_DS08260,BMG_DS032347,Deficiency of aromatic-L-amino-acid decarboxylase
+BMGC_DS08261,BMG_DS032389,Deficiency of maleylacetoacetate isomerase
+BMGC_DS08262,BMG_DS032391,Ribose 5-Phosphate Isomerase Deficiency
+BMGC_DS08263,BMG_DS032402,Deficiency of bisphosphoglycerate mutase
+BMGC_DS08264,BMG_DS032437,primary mediastinal large B-cell lymphoma
+BMGC_DS08265,BMG_DS032438,T-lymphoblastic lymphoma
+BMGC_DS08266,BMG_DS032440,"atypical chronic myeloid leukemia, BCR-ABL1 negative"
+BMGC_DS08267,BMG_DS032441,acute myeloid leukemia with multilineage dysplasia
+BMGC_DS08268,BMG_DS032442,acute myeloid leukemia with t(8;21)(q22;q22) translocation
+BMGC_DS08269,BMG_DS032443,acute myeloid leukemia with 11q23 abnormalities
+BMGC_DS08270,BMG_DS032444,therapy related acute myeloid leukemia and myelodysplastic syndrome
+BMGC_DS08271,BMG_DS032445,aggressive NK-cell leukemia
+BMGC_DS08272,BMG_DS032446,myeloproliferative neoplasm
+BMGC_DS08273,BMG_DS032453,Oxalosis
+BMGC_DS08274,BMG_DS032456,cleft lip and alveolus
+BMGC_DS08275,BMG_DS032604,endocervical carcinoma
+BMGC_DS08276,BMG_DS032605,exocervical carcinoma
+BMGC_DS08277,BMG_DS032606,subglottis carcinoma
+BMGC_DS08278,BMG_DS032607,carcinoma of supraglottis
+BMGC_DS08279,BMG_DS032608,ovarian cancer
+BMGC_DS08280,BMG_DS032610,Left Main Coronary Artery Disease
+BMGC_DS08281,BMG_DS032638,Early cirrhosis
+BMGC_DS08282,BMG_DS032650,Postural Orthostatic Tachycardia Syndrome
+BMGC_DS08283,BMG_DS032661,Extravasation injury
+BMGC_DS08284,BMG_DS032676,Eosinophilic myositis (disorder)
+BMGC_DS08285,BMG_DS032717,neoplasm with perivascular epithelioid cell differentiation
+BMGC_DS08286,BMG_DS032718,Chronic enlargement of lacrimal gland
+BMGC_DS08287,BMG_DS032724,Genochondromatosis
+BMGC_DS08288,BMG_DS032731,"Thanatophoric dysplasia, type 2"
+BMGC_DS08289,BMG_DS032732,"Spondyloepimetaphyseal dysplasia, sponastrime type"
+BMGC_DS08290,BMG_DS032738,Brachydactyly syndrome type C
+BMGC_DS08291,BMG_DS032743,SAUL-WILSON SYNDROME
+BMGC_DS08292,BMG_DS032744,Transient neonatal hyperparathyroidism
+BMGC_DS08293,BMG_DS032749,atypical polypoid adenomyoma
+BMGC_DS08294,BMG_DS032752,prostate small cell carcinoma
+BMGC_DS08295,BMG_DS032757,mixed ductal-endocrine carcinoma of pancreas
+BMGC_DS08296,BMG_DS032764,acantholytic acanthoma
+BMGC_DS08297,BMG_DS032766,myelodysplastic/myeloproliferative neoplasm
+BMGC_DS08298,BMG_DS032767,acute leukemia of ambiguous lineage
+BMGC_DS08299,BMG_DS032769,primary cutaneous anaplastic large cell lymphoma
+BMGC_DS08300,BMG_DS032770,CD4+/CD56+ hematodermic neoplasm
+BMGC_DS08301,BMG_DS032771,dendritic cell sarcoma
+BMGC_DS08302,BMG_DS032772,systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
+BMGC_DS08303,BMG_DS032782,Severe visual impairment
+BMGC_DS08304,BMG_DS032784,Vaccinia keratitis
+BMGC_DS08305,BMG_DS032795,Hypertension with albuminuria
+BMGC_DS08306,BMG_DS032821,colorectal adenoma
+BMGC_DS08307,BMG_DS032825,prostate squamous cell carcinoma
+BMGC_DS08308,BMG_DS032827,chronic lymphocytic leukemia/small lymphocytic lymphoma
+BMGC_DS08309,BMG_DS032828,ovarian monodermal teratoma
+BMGC_DS08310,BMG_DS032844,"fascial dystrophy, congenital"
+BMGC_DS08311,BMG_DS032873,epidermolytic nevus
+BMGC_DS08312,BMG_DS032887,congenital fibrosis of extraocular muscles
+BMGC_DS08313,BMG_DS032896,congenital microcoria
+BMGC_DS08314,BMG_DS032899,Nicolaides Baraitser syndrome
+BMGC_DS08315,BMG_DS032905,Acute ST segment elevation myocardial infarction (disorder)
+BMGC_DS08316,BMG_DS033048,Idiopathic angioedema
+BMGC_DS08317,BMG_DS033060,Autoimmune Urticaria
+BMGC_DS08318,BMG_DS033062,Chronic Autoimmune Urticaria
+BMGC_DS08319,BMG_DS033105,Familial localized cutaneous amyloidosis
+BMGC_DS08320,BMG_DS033124,adamantinoid basal cell epithelioma
+BMGC_DS08321,BMG_DS033127,nodular basal cell carcinoma
+BMGC_DS08322,BMG_DS033271,Linear and whorled nevoid hypermelanosis
+BMGC_DS08323,BMG_DS033276,spindle cell hemangioma
+BMGC_DS08324,BMG_DS033277,subungual glomus tumor
+BMGC_DS08325,BMG_DS033278,glomeruloid hemangioma
+BMGC_DS08326,BMG_DS033281,Ischemic fasciitis
+BMGC_DS08327,BMG_DS033289,"Thoracoabdominal aortic aneurysm, ruptured"
+BMGC_DS08328,BMG_DS033292,infiltrating angiolipoma
+BMGC_DS08329,BMG_DS033296,Fibroadenosis of breast
+BMGC_DS08330,BMG_DS033298,Familial hematuria
+BMGC_DS08331,BMG_DS033302,benign mammary dysplasia
+BMGC_DS08332,BMG_DS033321,developmental dysplasia of the hip 1
+BMGC_DS08333,BMG_DS033324,Oguchi disease
+BMGC_DS08334,BMG_DS033328,ACTH-producing pituitary gland adenoma
+BMGC_DS08335,BMG_DS033333,melanotic neurilemmoma
+BMGC_DS08336,BMG_DS033338,omphalocele | umbilical hernia
+BMGC_DS08337,BMG_DS033339,Chronic venous insufficiency
+BMGC_DS08338,BMG_DS033341,botryoid rhabdomyosarcoma
+BMGC_DS08339,BMG_DS033344,Acute encephalopathy
+BMGC_DS08340,BMG_DS033345,"Congenital dyserythropoietic anemia, type II"
+BMGC_DS08341,BMG_DS033357,Wound Botulism
+BMGC_DS08342,BMG_DS033362,Subacute lymphocytic thyroiditis
+BMGC_DS08343,BMG_DS033364,Periarthritis of shoulder
+BMGC_DS08344,BMG_DS033365,papillary renal cell carcinoma
+BMGC_DS08345,BMG_DS033366,Proliferative arthritis
+BMGC_DS08346,BMG_DS033375,Peripheral arterial occlusive disease
+BMGC_DS08347,BMG_DS033377,Hereditary edema of legs
+BMGC_DS08348,BMG_DS033380,Trichorrhexis nodosa syndrome
+BMGC_DS08349,BMG_DS033383,Acute contagious conjunctivitis
+BMGC_DS08350,BMG_DS033386,Hypertension complicating childbirth
+BMGC_DS08351,BMG_DS033388,Impetigo herpetiformis
+BMGC_DS08352,BMG_DS033398,Necrotizing vasculitis
+BMGC_DS08353,BMG_DS033400,secondary polycythemia
+BMGC_DS08354,BMG_DS033401,tenosynovial giant cell tumor
+BMGC_DS08355,BMG_DS033403,myelodysplastic syndrome with excess blasts-1
+BMGC_DS08356,BMG_DS033405,large congenital melanocytic nevus
+BMGC_DS08357,BMG_DS033406,Fusospirochetal pharyngitis
+BMGC_DS08358,BMG_DS033417,Staphylococcus aureus infection
+BMGC_DS08359,BMG_DS033442,colorectal adenocarcinoma
+BMGC_DS08360,BMG_DS033443,pharyngeal squamous cell carcinoma
+BMGC_DS08361,BMG_DS033448,Barber Say syndrome
+BMGC_DS08362,BMG_DS033453,"Asthma, Aspirin-Induced"
+BMGC_DS08363,BMG_DS033476,Infection caused by Enterococcus
+BMGC_DS08364,BMG_DS033518,cellular congenital mesoblastic nephroma
+BMGC_DS08365,BMG_DS033520,Allergic otitis externa
+BMGC_DS08366,BMG_DS033523,Peripheral retinal degeneration
+BMGC_DS08367,BMG_DS033538,Drug-induced Hepatic Necrosis
+BMGC_DS08368,BMG_DS033551,Paraneoplastic hyponatremia
+BMGC_DS08369,BMG_DS033555,mixed germ cell-sex cord-stromal tumor
+BMGC_DS08370,BMG_DS033578,epithelioid malignant peripheral nerve sheath tumor
+BMGC_DS08371,BMG_DS033589,Behçet's disease affecting oral mucosa
+BMGC_DS08372,BMG_DS033591,Muir-Torre syndrome
+BMGC_DS08373,BMG_DS033595,"acromegaloid changes, cutis verticis gyrata, and corneal leukoma"
+BMGC_DS08374,BMG_DS033599,Shprintzen-Goldberg syndrome
+BMGC_DS08375,BMG_DS033604,melanoacanthoma
+BMGC_DS08376,BMG_DS033605,melanotic psammomatous malignant peripheral nerve sheath tumor
+BMGC_DS08377,BMG_DS033609,Gestosis
+BMGC_DS08378,BMG_DS033611,childhood astrocytic tumor
+BMGC_DS08379,BMG_DS033612,pediatric intraocular retinoblastoma
+BMGC_DS08380,BMG_DS033613,pediatric extraocular retinoblastoma
+BMGC_DS08381,BMG_DS033616,sweat gland cancer
+BMGC_DS08382,BMG_DS033619,chordoid glioma of the third ventricle
+BMGC_DS08383,BMG_DS033622,type C thymoma
+BMGC_DS08384,BMG_DS033624,rectosigmoid carcinoma
+BMGC_DS08385,BMG_DS033625,congenital amegakaryocytic thrombocytopenia
+BMGC_DS08386,BMG_DS033626,Revesz syndrome
+BMGC_DS08387,BMG_DS033628,Oculootoradial syndrome
+BMGC_DS08388,BMG_DS033629,Myelocerebellar Disorder
+BMGC_DS08389,BMG_DS033630,thymoma type B
+BMGC_DS08390,BMG_DS033632,Mucocutaneous leishmaniasis
+BMGC_DS08391,BMG_DS033635,"Neuropathy, Ataxia, and Retinitis Pigmentosa"
+BMGC_DS08392,BMG_DS033636,Laryngoonychocutaneous syndrome
+BMGC_DS08393,BMG_DS033638,breast adenoma
+BMGC_DS08394,BMG_DS033641,pancreatic endocrine carcinoma
+BMGC_DS08395,BMG_DS033643,castration-resistant prostate carcinoma
+BMGC_DS08396,BMG_DS033644,invasive tubular breast carcinoma
+BMGC_DS08397,BMG_DS033645,Empty follicle syndrome
+BMGC_DS08398,BMG_DS033646,Autoimmune Lymphoproliferative Syndrome
+BMGC_DS08399,BMG_DS033651,extrahepatic bile duct adenoma
+BMGC_DS08400,BMG_DS033652,intrahepatic bile duct adenoma
+BMGC_DS08401,BMG_DS033654,thymic dysplasia
+BMGC_DS08402,BMG_DS033657,scrotum melanoma
+BMGC_DS08403,BMG_DS033660,ALK-positive anaplastic large cell lymphoma
+BMGC_DS08404,BMG_DS033661,neonatal abstinence syndrome
+BMGC_DS08405,BMG_DS033662,Achard syndrome
+BMGC_DS08406,BMG_DS033663,acinar lung adenocarcinoma
+BMGC_DS08407,BMG_DS033664,prostatic acinar adenocarcinoma
+BMGC_DS08408,BMG_DS033665,acrofacial dysostosis
+BMGC_DS08409,BMG_DS033666,acute hemorrhagic encephalitis
+BMGC_DS08410,BMG_DS033669,adenoid cystic breast carcinoma
+BMGC_DS08411,BMG_DS033670,thymic adenosquamous carcinoma
+BMGC_DS08412,BMG_DS033672,adrenal gland ganglioneuroblastoma
+BMGC_DS08413,BMG_DS033674,adult astrocytic tumor
+BMGC_DS08414,BMG_DS033675,adult botryoid rhabdomyosarcoma
+BMGC_DS08415,BMG_DS033676,adult brain ependymoma
+BMGC_DS08416,BMG_DS033677,adult oligodendroglioma
+BMGC_DS08417,BMG_DS033678,adult brainstem astrocytoma
+BMGC_DS08418,BMG_DS033679,adult brain stem neoplasm
+BMGC_DS08419,BMG_DS033680,adult central nervous system immature teratoma
+BMGC_DS08420,BMG_DS033681,adult central nervous system mature teratoma
+BMGC_DS08421,BMG_DS033682,adult central nervous system mixed germ cell tumor
+BMGC_DS08422,BMG_DS033684,adult cerebellar neoplasm
+BMGC_DS08423,BMG_DS033685,clear cell sarcoma
+BMGC_DS08424,BMG_DS033687,adult leptomeningeal melanoma
+BMGC_DS08425,BMG_DS033688,adult lymphoma
+BMGC_DS08426,BMG_DS033689,adult mesenchymal chondrosarcoma
+BMGC_DS08427,BMG_DS033691,adult pleomorphic rhabdomyosarcoma
+BMGC_DS08428,BMG_DS033692,adult spinal cord ependymoma
+BMGC_DS08429,BMG_DS033693,adult kidney Wilms tumor
+BMGC_DS08430,BMG_DS033694,adult xanthogranuloma
+BMGC_DS08431,BMG_DS033695,adult yolk sac tumor
+BMGC_DS08432,BMG_DS033696,aflatoxin-related hepatocellular carcinoma
+BMGC_DS08433,BMG_DS033697,aleukemic monocytic leukemia cutis
+BMGC_DS08434,BMG_DS033699,ampulla of vater adenocarcinoma
+BMGC_DS08435,BMG_DS033700,ampulla of vater adenosquamous carcinoma
+BMGC_DS08436,BMG_DS033701,ampulla of vater clear cell adenocarcinoma
+BMGC_DS08437,BMG_DS033702,ampulla of vater mucinous adenocarcinoma
+BMGC_DS08438,BMG_DS033703,ampullary signet ring cell adenocarcinoma
+BMGC_DS08439,BMG_DS033704,ampulla of vater small cell neuroendocrine carcinoma
+BMGC_DS08440,BMG_DS033705,ampulla of vater squamous cell carcinoma
+BMGC_DS08441,BMG_DS033706,anus adenocarcinoma
+BMGC_DS08442,BMG_DS033707,anal canal adenocarcinoma
+BMGC_DS08443,BMG_DS033708,anal canal Paget disease
+BMGC_DS08444,BMG_DS033710,Kaposi's sarcoma
+BMGC_DS08445,BMG_DS033712,anus leiomyosarcoma
+BMGC_DS08446,BMG_DS033713,anus lymphoma
+BMGC_DS08447,BMG_DS033714,anal margin basal cell carcinoma
+BMGC_DS08448,BMG_DS033715,perianal skin Paget disease
+BMGC_DS08449,BMG_DS033716,anal mucinous adenocarcinoma
+BMGC_DS08450,BMG_DS033717,anal canal neuroendocrine neoplasm
+BMGC_DS08451,BMG_DS033718,anal Paget disease
+BMGC_DS08452,BMG_DS033719,anus rhabdomyosarcoma
+BMGC_DS08453,BMG_DS033720,anus sarcoma
+BMGC_DS08454,BMG_DS033721,anal verrucous carcinoma
+BMGC_DS08455,BMG_DS033723,anterior cranial fossa meningioma
+BMGC_DS08456,BMG_DS033724,anterior foramen magnum meningioma
+BMGC_DS08457,BMG_DS033725,anterior optic tract meningioma
+BMGC_DS08458,BMG_DS033726,anti-basement membrane glomerulonephritis
+BMGC_DS08459,BMG_DS033727,aorta angiosarcoma
+BMGC_DS08460,BMG_DS033728,apocrine adenosis of breast
+BMGC_DS08461,BMG_DS033729,breast apocrine carcinoma in situ
+BMGC_DS08462,BMG_DS033730,breast apocrine carcinoma
+BMGC_DS08463,BMG_DS033731,apocrine sweat gland neoplasm
+BMGC_DS08464,BMG_DS033733,appendix lymphoma
+BMGC_DS08465,BMG_DS033735,asbestos-related lung carcinoma
+BMGC_DS08466,BMG_DS033736,malignant mesothelioma
+BMGC_DS08467,BMG_DS033738,asymmetric motor neuropathy
+BMGC_DS08468,BMG_DS033739,asynchronous multifocal osteogenic sarcoma
+BMGC_DS08469,BMG_DS033740,atypical breast papilloma
+BMGC_DS08470,BMG_DS033741,autoimmune hepatitis
+BMGC_DS08471,BMG_DS033742,autonomic nervous system neoplasm
+BMGC_DS08472,BMG_DS033743,Barrett adenocarcinoma
+BMGC_DS08473,BMG_DS033744,basaloid carcinoma of the penis
+BMGC_DS08474,BMG_DS033745,basaloid large cell lung carcinoma
+BMGC_DS08475,BMG_DS033746,thymic basaloid carcinoma
+BMGC_DS08476,BMG_DS033748,benign dermal neurilemmoma
+BMGC_DS08477,BMG_DS033752,benign mediastinal psammomatous neurilemmoma
+BMGC_DS08478,BMG_DS033753,mesenchymal cell neoplasm
+BMGC_DS08479,BMG_DS033757,benign perivascular tumor
+BMGC_DS08480,BMG_DS033763,bilateral meningioma of optic nerve
+BMGC_DS08481,BMG_DS033764,extrahepatic bile duct mucoepidermoid carcinoma
+BMGC_DS08482,BMG_DS033765,classic pulmonary blastoma
+BMGC_DS08483,BMG_DS033766,bladder clear cell adenocarcinoma
+BMGC_DS08484,BMG_DS033769,bladder lymphoma
+BMGC_DS08485,BMG_DS033770,bladder signet ring cell adenocarcinoma
+BMGC_DS08486,BMG_DS033771,urinary bladder small cell neuroendocrine carcinoma
+BMGC_DS08487,BMG_DS033775,bone leiomyosarcoma
+BMGC_DS08488,BMG_DS033776,liposarcoma of bone
+BMGC_DS08489,BMG_DS033777,primary bone lymphoma
+BMGC_DS08490,BMG_DS033778,peripheral osteosarcoma
+BMGC_DS08491,BMG_DS033780,brachial plexus neoplasm
+BMGC_DS08492,BMG_DS033781,brain germinoma
+BMGC_DS08493,BMG_DS033782,brain sarcoma
+BMGC_DS08494,BMG_DS033783,brain stem astrocytic neoplasm
+BMGC_DS08495,BMG_DS033784,brain stem ependymoma
+BMGC_DS08496,BMG_DS033785,brain stem hemangioblastoma
+BMGC_DS08497,BMG_DS033786,brainstem intraparenchymal clear cell meningioma
+BMGC_DS08498,BMG_DS033787,breast angiosarcoma
+BMGC_DS08499,BMG_DS033788,breast capillary hemangioma
+BMGC_DS08500,BMG_DS033789,breast epithelioid hemangioma
+BMGC_DS08501,BMG_DS033790,non-proliferative fibrocystic change of the breast
+BMGC_DS08502,BMG_DS033792,breast fibrosarcoma
+BMGC_DS08503,BMG_DS033793,breast leiomyosarcoma
+BMGC_DS08504,BMG_DS033794,breast liposarcoma
+BMGC_DS08505,BMG_DS033797,breast rhabdomyosarcoma
+BMGC_DS08506,BMG_DS033798,lung mucous gland adenoma
+BMGC_DS08507,BMG_DS033800,Complement component 3 deficiency
+BMGC_DS08508,BMG_DS033802,carcinoma arising in nasal papillomatosis
+BMGC_DS08509,BMG_DS033803,heart fibrosarcoma
+BMGC_DS08510,BMG_DS033805,Kaposi's sarcoma
+BMGC_DS08511,BMG_DS033806,heart leiomyosarcoma
+BMGC_DS08512,BMG_DS033807,heart lipoma
+BMGC_DS08513,BMG_DS033808,heart lymphoma
+BMGC_DS08514,BMG_DS033809,cardiac rhabdomyoma
+BMGC_DS08515,BMG_DS033811,cavernous hemangioma of face
+BMGC_DS08516,BMG_DS033812,cavernous sinus meningioma
+BMGC_DS08517,BMG_DS033813,cecum adenocarcinoma
+BMGC_DS08518,BMG_DS033814,cecum lymphoma
+BMGC_DS08519,BMG_DS033816,central nervous system angiosarcoma
+BMGC_DS08520,BMG_DS033818,central nervous system fibrosarcoma
+BMGC_DS08521,BMG_DS033819,central nervous system germ cell tumor
+BMGC_DS08522,BMG_DS033820,central nervous system hematopoietic neoplasm
+BMGC_DS08523,BMG_DS033821,central nervous system immature teratoma
+BMGC_DS08524,BMG_DS033822,central nervous system leukemia
+BMGC_DS08525,BMG_DS033823,central nervous system lipoma
+BMGC_DS08526,BMG_DS033824,central nervous system mature teratoma
+BMGC_DS08527,BMG_DS033825,central nervous system melanocytic neoplasm
+BMGC_DS08528,BMG_DS033826,central nervous system rhabdomyosarcoma
+BMGC_DS08529,BMG_DS033827,central nervous system sarcoma
+BMGC_DS08530,BMG_DS033829,central nervous system teratoma
+BMGC_DS08531,BMG_DS033830,central breast papilloma
+BMGC_DS08532,BMG_DS033831,cerebellar hemangioblastoma
+BMGC_DS08533,BMG_DS033832,papillary meningioma of the cerebellum
+BMGC_DS08534,BMG_DS033836,cerebral hemisphere lipoma
+BMGC_DS08535,BMG_DS033837,cervical adenoid cystic carcinoma
+BMGC_DS08536,BMG_DS033838,cervical clear cell adenocarcinoma
+BMGC_DS08537,BMG_DS033839,cervical endometrioid adenocarcinoma
+BMGC_DS08538,BMG_DS033840,cervical spinal canal and spinal cord meningioma
+BMGC_DS08539,BMG_DS033841,cervical carcinosarcoma
+BMGC_DS08540,BMG_DS033842,cervical mucinous adenocarcinoma
+BMGC_DS08541,BMG_DS033844,cervicomedullary junction neoplasm
+BMGC_DS08542,BMG_DS033846,chest wall lymphoma
+BMGC_DS08543,BMG_DS033847,chest wall parachordoma
+BMGC_DS08544,BMG_DS033848,solitary plasmacytoma of chest wall
+BMGC_DS08545,BMG_DS033849,childhood botryoid rhabdomyosarcoma
+BMGC_DS08546,BMG_DS033850,childhood vagina botryoid rhabdomyosarcoma
+BMGC_DS08547,BMG_DS033851,vulvar childhood botryoid-type embryonal rhabdomyosarcoma
+BMGC_DS08548,BMG_DS033852,childhood brain germinoma
+BMGC_DS08549,BMG_DS033854,childhood brainstem astrocytoma
+BMGC_DS08550,BMG_DS033855,childhood brain stem neoplasm
+BMGC_DS08551,BMG_DS033856,childhood central nervous system germinoma
+BMGC_DS08552,BMG_DS033857,childhood central nervous system immature teratoma
+BMGC_DS08553,BMG_DS033858,childhood central nervous system mature teratoma
+BMGC_DS08554,BMG_DS033859,childhood central nervous system mixed germ cell tumor
+BMGC_DS08555,BMG_DS033861,childhood cerebellar neoplasm
+BMGC_DS08556,BMG_DS033864,congenital mesoblastic nephroma
+BMGC_DS08557,BMG_DS033865,childhood extraosseous osteosarcoma
+BMGC_DS08558,BMG_DS033867,pediatric infratentorial ependymoblastoma
+BMGC_DS08559,BMG_DS033868,childhood infratentorial neoplasm
+BMGC_DS08560,BMG_DS033869,childhood intracortical osteosarcoma
+BMGC_DS08561,BMG_DS033870,pediatric leptomeningeal melanoma
+BMGC_DS08562,BMG_DS033871,childhood leukemia
+BMGC_DS08563,BMG_DS033872,pediatric lymphoma
+BMGC_DS08564,BMG_DS033873,childhood mediastinal neurogenic neoplasm
+BMGC_DS08565,BMG_DS033874,pediatric mesenchymal chondrosarcoma
+BMGC_DS08566,BMG_DS033875,childhood multilocular cystic kidney neoplasm
+BMGC_DS08567,BMG_DS033876,pediatric myxoid chondrosarcoma
+BMGC_DS08568,BMG_DS033877,pediatric osteosarcoma
+BMGC_DS08569,BMG_DS033878,childhood choriocarcinoma of the ovary
+BMGC_DS08570,BMG_DS033879,pediatric ovarian dysgerminoma
+BMGC_DS08571,BMG_DS033880,childhood ovarian embryonal carcinoma
+BMGC_DS08572,BMG_DS033881,childhood immature teratoma of ovary
+BMGC_DS08573,BMG_DS033882,childhood mature teratoma of the ovary
+BMGC_DS08574,BMG_DS033883,childhood teratoma of the ovary
+BMGC_DS08575,BMG_DS033884,childhood ovarian yolk sac tumor
+BMGC_DS08576,BMG_DS033885,childhood parosteal osteosarcoma
+BMGC_DS08577,BMG_DS033886,childhood pilocytic astrocytoma
+BMGC_DS08578,BMG_DS033889,childhood kidney angiomyolipoma
+BMGC_DS08579,BMG_DS033890,childhood kidney cell carcinoma
+BMGC_DS08580,BMG_DS033891,childhood kidney neoplasm
+BMGC_DS08581,BMG_DS033892,childhood testicular choriocarcinoma
+BMGC_DS08582,BMG_DS033893,childhood embryonal testis carcinoma
+BMGC_DS08583,BMG_DS033894,childhood testicular mixed embryonal carcinoma and teratoma
+BMGC_DS08584,BMG_DS033895,childhood testicular mixed germ cell cancer
+BMGC_DS08585,BMG_DS033896,childhood testicular neoplasm
+BMGC_DS08586,BMG_DS033897,childhood optic tract astrocytoma
+BMGC_DS08587,BMG_DS033898,childhood kidney Wilms tumor
+BMGC_DS08588,BMG_DS033899,childhood endodermal sinus tumor
+BMGC_DS08589,BMG_DS033901,choroid epithelioid cell melanoma
+BMGC_DS08590,BMG_DS033902,choroid mixed cell melanoma
+BMGC_DS08591,BMG_DS033903,choroid necrotic melanoma
+BMGC_DS08592,BMG_DS033904,choroid spindle cell melanoma
+BMGC_DS08593,BMG_DS033905,chronic lymphocytic leukemia/small lymphocytic lymphoma with immunoglobulin heavy chain variable-region gene somatic hypermutation
+BMGC_DS08594,BMG_DS033906,pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma
+BMGC_DS08595,BMG_DS033907,chronic metabolic polyneuropathy
+BMGC_DS08596,BMG_DS033908,"myeloproliferative neoplasm, unclassifiable"
+BMGC_DS08597,BMG_DS033909,chronic toxic polyneuropathy
+BMGC_DS08598,BMG_DS033910,ciliary body epithelioid cell melanoma
+BMGC_DS08599,BMG_DS033911,ciliary body mixed cell melanoma
+BMGC_DS08600,BMG_DS033912,ciliary body spindle cell melanoma
+BMGC_DS08601,BMG_DS033913,conventional lipoma
+BMGC_DS08602,BMG_DS033914,classic variant of chromophobe renal cell carcinoma
+BMGC_DS08603,BMG_DS033915,clear cell-sugar-tumor of the lung
+BMGC_DS08604,BMG_DS033916,thymus clear cell carcinoma
+BMGC_DS08605,BMG_DS033917,clitoral carcinoma
+BMGC_DS08606,BMG_DS033918,clivus chordoma
+BMGC_DS08607,BMG_DS033919,clivus chondroid chordoma
+BMGC_DS08608,BMG_DS033920,clivus meningioma
+BMGC_DS08609,BMG_DS033921,rectal cloacogenic carcinoma
+BMGC_DS08610,BMG_DS033922,colloid carcinoma of the pancreas
+BMGC_DS08611,BMG_DS033923,adenosquamous colon carcinoma
+BMGC_DS08612,BMG_DS033926,cavernous hemangioma of colon
+BMGC_DS08613,BMG_DS033928,colon Kaposi sarcoma
+BMGC_DS08614,BMG_DS033929,colon leiomyoma
+BMGC_DS08615,BMG_DS033930,colon leiomyosarcoma
+BMGC_DS08616,BMG_DS033931,colonic lymphangioma
+BMGC_DS08617,BMG_DS033933,colon neuroendocrine neoplasm
+BMGC_DS08618,BMG_DS033934,colon sarcoma
+BMGC_DS08619,BMG_DS033935,colon small cell neuroendocrine carcinoma
+BMGC_DS08620,BMG_DS033936,squamous cell carcinoma of colon
+BMGC_DS08621,BMG_DS033938,colorectal leiomyoma
+BMGC_DS08622,BMG_DS033939,colorectal lipoma
+BMGC_DS08623,BMG_DS033941,columnar cell variant thyroid gland papillary carcinoma
+BMGC_DS08624,BMG_DS033942,lung combined large cell neuroendocrine carcinoma
+BMGC_DS08625,BMG_DS033944,combined small cell lung carcinoma
+BMGC_DS08626,BMG_DS033945,breast fibroadenoma
+BMGC_DS08627,BMG_DS033946,congenital T-cell immunodeficiency
+BMGC_DS08628,BMG_DS033947,conjunctival intraepithelial neoplasm
+BMGC_DS08629,BMG_DS033948,conus medullaris neoplasm
+BMGC_DS08630,BMG_DS033949,conventional angiosarcoma
+BMGC_DS08631,BMG_DS033950,conventional fibrosarcoma
+BMGC_DS08632,BMG_DS033951,conventional leiomyosarcoma
+BMGC_DS08633,BMG_DS033952,conventional malignant hemangiopericytoma
+BMGC_DS08634,BMG_DS033953,corneal intraepithelial neoplasm
+BMGC_DS08635,BMG_DS033954,corpus callosum lipoma
+BMGC_DS08636,BMG_DS033955,cranial nodular fasciitis
+BMGC_DS08637,BMG_DS033957,skin lipoma
+BMGC_DS08638,BMG_DS033958,cutaneous liposarcoma
+BMGC_DS08639,BMG_DS033959,skin lymphangioma
+BMGC_DS08640,BMG_DS033961,deep hemangioma
+BMGC_DS08641,BMG_DS033962,deep leiomyoma
+BMGC_DS08642,BMG_DS033963,spinal cord dermoid cyst
+BMGC_DS08643,BMG_DS033965,diaphragma sellae meningioma
+BMGC_DS08644,BMG_DS033966,diencephalic astrocytomas
+BMGC_DS08645,BMG_DS033967,diencephalic neoplasm
+BMGC_DS08646,BMG_DS033969,Diffuse infiltrative lymphocytosis syndrome
+BMGC_DS08647,BMG_DS033973,diffuse lipomatosis
+BMGC_DS08648,BMG_DS033974,peripheral epithelioid sarcoma
+BMGC_DS08649,BMG_DS033975,distal biliary tract carcinoma
+BMGC_DS08650,BMG_DS033976,duodenal somatostatinoma
+BMGC_DS08651,BMG_DS033977,duodenal gastrin-producing neuroendocrine tumor
+BMGC_DS08652,BMG_DS033980,early invasive cervical adenocarcinoma
+BMGC_DS08653,BMG_DS033981,microinvasive cervical squamous cell carcinoma
+BMGC_DS08654,BMG_DS033982,eccrine sweat gland neoplasm
+BMGC_DS08655,BMG_DS033984,Ectopic thymus
+BMGC_DS08656,BMG_DS033985,embryonal carcinoma of the central nervous system
+BMGC_DS08657,BMG_DS033986,encapsulated thymoma
+BMGC_DS08658,BMG_DS033987,endobronchial leiomyoma
+BMGC_DS08659,BMG_DS033988,endometrial squamous cell carcinoma
+BMGC_DS08660,BMG_DS033989,eosinophilic variant of chromophobe renal cell carcinoma
+BMGC_DS08661,BMG_DS033990,ependymal tumor
+BMGC_DS08662,BMG_DS033991,epicardium lipoma
+BMGC_DS08663,BMG_DS033992,epidermolytic acanthoma
+BMGC_DS08664,BMG_DS033994,epidural spinal canal angiolipoma
+BMGC_DS08665,BMG_DS033995,epidural spinal canal meningioma
+BMGC_DS08666,BMG_DS033996,liver benign neoplasm
+BMGC_DS08667,BMG_DS033997,epithelial predominant pulmonary blastoma
+BMGC_DS08668,BMG_DS033998,epithelioid cell uveal melanoma
+BMGC_DS08669,BMG_DS034000,esophageal adenoid cystic carcinoma
+BMGC_DS08670,BMG_DS034001,esophageal basaloid carcinoma
+BMGC_DS08671,BMG_DS034002,esophageal granular cell tumor
+BMGC_DS08672,BMG_DS034003,Kaposi's sarcoma
+BMGC_DS08673,BMG_DS034004,esophagus leiomyosarcoma
+BMGC_DS08674,BMG_DS034006,esophagus liposarcoma
+BMGC_DS08675,BMG_DS034007,esophagus lymphoma
+BMGC_DS08676,BMG_DS034008,esophageal melanoma
+BMGC_DS08677,BMG_DS034009,mucoepidermoid esophageal carcinoma
+BMGC_DS08678,BMG_DS034010,esophageal neuroendocrine tumor
+BMGC_DS08679,BMG_DS034011,neurofibroma of the esophagus
+BMGC_DS08680,BMG_DS034012,esophagus sarcoma
+BMGC_DS08681,BMG_DS034014,esophagus verrucous carcinoma
+BMGC_DS08682,BMG_DS034015,ethmoid sinus adenocarcinoma
+BMGC_DS08683,BMG_DS034016,ethmoid sinus adenoid cystic carcinoma
+BMGC_DS08684,BMG_DS034017,ethmoid sinus inverted papilloma
+BMGC_DS08685,BMG_DS034018,ethmoid sinus ectopic meningioma
+BMGC_DS08686,BMG_DS034019,ethmoid sinus Schneiderian papilloma
+BMGC_DS08687,BMG_DS034020,ethmoid sinus squamous cell carcinoma
+BMGC_DS08688,BMG_DS034021,Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone
+BMGC_DS08689,BMG_DS034023,external ear basal cell carcinoma
+BMGC_DS08690,BMG_DS034024,external ear carcinoma
+BMGC_DS08691,BMG_DS034025,external ear squamous cell carcinoma
+BMGC_DS08692,BMG_DS034026,extracranial neuroblastoma
+BMGC_DS08693,BMG_DS034027,extragonadal seminoma
+BMGC_DS08694,BMG_DS034028,extrahepatic bile duct cystadenoma
+BMGC_DS08695,BMG_DS034029,embryonal extrahepatic bile duct rhabdomyosarcoma
+BMGC_DS08696,BMG_DS034031,extrahepatic bile duct leiomyosarcoma
+BMGC_DS08697,BMG_DS034032,extrahepatic bile duct lipoma
+BMGC_DS08698,BMG_DS034033,extrahepatic bile duct papillary adenoma
+BMGC_DS08699,BMG_DS034034,extrahepatic biliary papillomatosis
+BMGC_DS08700,BMG_DS034035,extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor
+BMGC_DS08701,BMG_DS034036,fallopian tube adenocarcinoma
+BMGC_DS08702,BMG_DS034037,fallopian tube clear cell adenocarcinoma
+BMGC_DS08703,BMG_DS034038,fallopian tube endometrioid adenocarcinoma
+BMGC_DS08704,BMG_DS034039,fallopian tube gestational choriocarcinoma
+BMGC_DS08705,BMG_DS034040,fallopian tube papillary adenocarcinoma
+BMGC_DS08706,BMG_DS034041,fallopian tube squamous cell carcinoma
+BMGC_DS08707,BMG_DS034042,cerebral falx meningioma
+BMGC_DS08708,BMG_DS034044,fibrous synovial sarcoma
+BMGC_DS08709,BMG_DS034045,flat ductal epithelial atypia
+BMGC_DS08710,BMG_DS034049,foramen magnum meningioma
+BMGC_DS08711,BMG_DS034050,frontal convexity meningioma
+BMGC_DS08712,BMG_DS034051,frontal sinus inverted papilloma
+BMGC_DS08713,BMG_DS034052,frontal sinus Schneiderian papilloma
+BMGC_DS08714,BMG_DS034053,frontal sinus squamous cell carcinoma
+BMGC_DS08715,BMG_DS034054,gallbladder adenosquamous carcinoma
+BMGC_DS08716,BMG_DS034055,gallbladder angiosarcoma
+BMGC_DS08717,BMG_DS034056,Kaposi's sarcoma
+BMGC_DS08718,BMG_DS034058,gallbladder leiomyosarcoma
+BMGC_DS08719,BMG_DS034060,gallbladder lymphoma
+BMGC_DS08720,BMG_DS034061,gallbladder melanoma
+BMGC_DS08721,BMG_DS034062,gallbladder mucinous adenocarcinoma
+BMGC_DS08722,BMG_DS034063,neurofibroma of gallbladder
+BMGC_DS08723,BMG_DS034066,gallbladder rhabdomyosarcoma
+BMGC_DS08724,BMG_DS034067,gallbladder sarcoma
+BMGC_DS08725,BMG_DS034068,gallbladder signet ring cell adenocarcinoma
+BMGC_DS08726,BMG_DS034069,gallbladder small cell neuroendocrine carcinoma
+BMGC_DS08727,BMG_DS034070,gasserian ganglion meningioma
+BMGC_DS08728,BMG_DS034071,gastric adenosquamous carcinoma
+BMGC_DS08729,BMG_DS034072,gastric cardia adenocarcinoma
+BMGC_DS08730,BMG_DS034073,gastric cardia carcinoma
+BMGC_DS08731,BMG_DS034074,Cronkhite-Canada syndrome
+BMGC_DS08732,BMG_DS034075,gastric gastrin-producing neuroendocrine tumor
+BMGC_DS08733,BMG_DS034076,malignant gastric germ cell tumor
+BMGC_DS08734,BMG_DS034078,Kaposi's sarcoma
+BMGC_DS08735,BMG_DS034080,gastric liposarcoma
+BMGC_DS08736,BMG_DS034083,gastric neuroendocrine neoplasm
+BMGC_DS08737,BMG_DS034085,gastric papillary adenocarcinoma
+BMGC_DS08738,BMG_DS034086,gastric pylorus carcinoma
+BMGC_DS08739,BMG_DS034087,gastric small cell neuroendocrine carcinoma
+BMGC_DS08740,BMG_DS034088,gastric squamous cell carcinoma
+BMGC_DS08741,BMG_DS034089,gastric teratoma
+BMGC_DS08742,BMG_DS034090,gastric tubular adenocarcinoma
+BMGC_DS08743,BMG_DS034092,digestive system neuroendocrine neoplasm
+BMGC_DS08744,BMG_DS034093,central nervous system germinoma
+BMGC_DS08745,BMG_DS034094,giant hemangioma
+BMGC_DS08746,BMG_DS034095,malignant glandular tumor of peripheral nerve sheath
+BMGC_DS08747,BMG_DS034096,glomangiomatosis
+BMGC_DS08748,BMG_DS034097,granular cell leiomyosarcoma
+BMGC_DS08749,BMG_DS034098,neurohypophysis granular cell tumor
+BMGC_DS08750,BMG_DS034099,granulomatous endometritis
+BMGC_DS08751,BMG_DS034100,"B-cell lymphoma, unclassifiable, with features intermediate between diffuse large b-cell lymphoma and classical Hodgkin lymphoma"
+BMGC_DS08752,BMG_DS034105,hepatic angiomyolipoma
+BMGC_DS08753,BMG_DS034106,liver solitary fibrous tumor
+BMGC_DS08754,BMG_DS034107,liver fibrosarcoma
+BMGC_DS08755,BMG_DS034108,liver inflammatory myofibroblastic tumor
+BMGC_DS08756,BMG_DS034109,liver leiomyoma
+BMGC_DS08757,BMG_DS034110,liver leiomyosarcoma
+BMGC_DS08758,BMG_DS034111,liver lipoma
+BMGC_DS08759,BMG_DS034113,liver extraskeletal osteosarcoma
+BMGC_DS08760,BMG_DS034114,liver rhabdomyosarcoma
+BMGC_DS08761,BMG_DS034115,liver and intrahepatic bile duct neoplasm
+BMGC_DS08762,BMG_DS034116,hepatosplenic T-cell lymphoma
+BMGC_DS08763,BMG_DS034117,hereditary clear cell renal cell carcinoma
+BMGC_DS08764,BMG_DS034118,familial glomangioma
+BMGC_DS08765,BMG_DS034119,familial meningioma
+BMGC_DS08766,BMG_DS034120,hereditary nonpolyposis colon cancer
+BMGC_DS08767,BMG_DS034121,Lynch syndrome 2
+BMGC_DS08768,BMG_DS034122,familial ovarian carcinoma
+BMGC_DS08769,BMG_DS034123,herpetic gastritis
+BMGC_DS08770,BMG_DS034126,histiocytic and dendritic cell neoplasm
+BMGC_DS08771,BMG_DS034129,hypercalcemic sarcoidosis
+BMGC_DS08772,BMG_DS034130,hyperimmunoglobulin syndrome
+BMGC_DS08773,BMG_DS034132,idiopathic granulomatous myositis
+BMGC_DS08774,BMG_DS034133,immature gastric teratoma
+BMGC_DS08775,BMG_DS034136,inflammatory leiomyosarcoma
+BMGC_DS08776,BMG_DS034137,"undifferentiated pleomorphic sarcoma, inflammatory variant"
+BMGC_DS08777,BMG_DS034138,intermediate cell type choroid melanoma
+BMGC_DS08778,BMG_DS034139,intermediate cell type ciliary body melanoma
+BMGC_DS08779,BMG_DS034140,intermediate cell type iris melanoma
+BMGC_DS08780,BMG_DS034142,internal auditory canal meningioma
+BMGC_DS08781,BMG_DS034143,intestinal neuroendocrine neoplasm
+BMGC_DS08782,BMG_DS034144,intracerebral cystic meningioma
+BMGC_DS08783,BMG_DS034145,intracranial cavernous angioma
+BMGC_DS08784,BMG_DS034146,intracranial extraskeletal myxoid chondrosarcoma
+BMGC_DS08785,BMG_DS034147,intracranial liposarcoma
+BMGC_DS08786,BMG_DS034151,intraductal papillary breast neoplasm
+BMGC_DS08787,BMG_DS034152,cauda equina intradural extramedullary astrocytoma
+BMGC_DS08788,BMG_DS034153,intradural extramedullary spinal canal neoplasm
+BMGC_DS08789,BMG_DS034154,intrahepatic bile duct cystadenoma
+BMGC_DS08790,BMG_DS034155,intrahepatic biliary papillomatosis
+BMGC_DS08791,BMG_DS034156,spinal cord intramedullary teratoma
+BMGC_DS08792,BMG_DS034157,intraorbital meningioma
+BMGC_DS08793,BMG_DS034158,intraspinal meningioma
+BMGC_DS08794,BMG_DS034159,intravascular angioleiomyoma
+BMGC_DS08795,BMG_DS034160,intraventricular meningioma
+BMGC_DS08796,BMG_DS034163,infiltrating bladder urothelial carcinoma
+BMGC_DS08797,BMG_DS034164,inverted urothelial papilloma
+BMGC_DS08798,BMG_DS034165,iris spindle cell melanoma
+BMGC_DS08799,BMG_DS034167,jejunal somatostatinoma
+BMGC_DS08800,BMG_DS034168,jugular foramen meningioma
+BMGC_DS08801,BMG_DS034169,schwannoma of jugular foramen
+BMGC_DS08802,BMG_DS034171,Kaposi's sarcoma
+BMGC_DS08803,BMG_DS034172,kidney benign neoplasm
+BMGC_DS08804,BMG_DS034173,labia majora carcinoma
+BMGC_DS08805,BMG_DS034174,labia minora carcinoma
+BMGC_DS08806,BMG_DS034175,lacrimal gland carcinoma
+BMGC_DS08807,BMG_DS034176,lacrimal gland mucoepidermoid carcinoma
+BMGC_DS08808,BMG_DS034178,lacrimal system cancer
+BMGC_DS08809,BMG_DS034179,large cell acanthoma
+BMGC_DS08810,BMG_DS034180,pulmonary large cell neuroendocrine carcinoma
+BMGC_DS08811,BMG_DS034181,thymic large cell neuroendocrine carcinoma
+BMGC_DS08812,BMG_DS034182,laryngeal adenoid cystic carcinoma
+BMGC_DS08813,BMG_DS034183,laryngeal leiomyoma
+BMGC_DS08814,BMG_DS034184,laryngeal leiomyosarcoma
+BMGC_DS08815,BMG_DS034185,larynx liposarcoma
+BMGC_DS08816,BMG_DS034186,laryngeal mucoepidermoid carcinoma
+BMGC_DS08817,BMG_DS034187,laryngeal neuroendocrine neoplasm
+BMGC_DS08818,BMG_DS034188,laryngeal sarcoma
+BMGC_DS08819,BMG_DS034189,laryngeal small cell carcinoma
+BMGC_DS08820,BMG_DS034190,lateral ventricle meningioma
+BMGC_DS08821,BMG_DS034193,leptomeningeal melanoma
+BMGC_DS08822,BMG_DS034194,Ewing sarcoma of bone
+BMGC_DS08823,BMG_DS034195,Ewing sarcoma
+BMGC_DS08824,BMG_DS034196,medulloblastoma
+BMGC_DS08825,BMG_DS034198,lower clivus meningioma
+BMGC_DS08826,BMG_DS034199,lumbar spinal canal and spinal cord meningioma
+BMGC_DS08827,BMG_DS034200,lumbar plexus neoplasm
+BMGC_DS08828,BMG_DS034202,lung adenoid cystic carcinoma
+BMGC_DS08829,BMG_DS034204,lung hilum carcinoma
+BMGC_DS08830,BMG_DS034205,lung leiomyoma
+BMGC_DS08831,BMG_DS034206,lung leiomyosarcoma
+BMGC_DS08832,BMG_DS034207,lung meningioma
+BMGC_DS08833,BMG_DS034208,lung neuroendocrine neoplasm
+BMGC_DS08834,BMG_DS034210,pulmonary sclerosing hemangioma
+BMGC_DS08835,BMG_DS034211,Kaposi's sarcoma
+BMGC_DS08836,BMG_DS034212,lymphohistiocytoid mesothelioma
+BMGC_DS08837,BMG_DS034213,macrotrabecular hepatoblastoma
+BMGC_DS08838,BMG_DS034218,ACTH-producing pituitary gland carcinoma
+BMGC_DS08839,BMG_DS034219,brain cancer
+BMGC_DS08840,BMG_DS034220,adult intracranial malignant hemangiopericytoma
+BMGC_DS08841,BMG_DS034221,aortic malignant tumor
+BMGC_DS08842,BMG_DS034222,apocrine sweat gland cancer
+BMGC_DS08843,BMG_DS034223,breast adenomyoepithelioma
+BMGC_DS08844,BMG_DS034224,breast malignant eccrine spiradenoma
+BMGC_DS08845,BMG_DS034225,malignant cardiac germ cell tumor
+BMGC_DS08846,BMG_DS034226,heart malignant hemangiopericytoma
+BMGC_DS08847,BMG_DS034227,malignant cardiac peripheral nerve sheath neoplasm
+BMGC_DS08848,BMG_DS034229,chest wall bone cancer
+BMGC_DS08849,BMG_DS034230,malignant childhood germ cell neoplasm
+BMGC_DS08850,BMG_DS034231,malignant cutaneous granular cell skin tumor
+BMGC_DS08851,BMG_DS034232,diencephalic cancer
+BMGC_DS08852,BMG_DS034233,eccrine sweat gland cancer
+BMGC_DS08853,BMG_DS034234,extragonadal germ cell cancer
+BMGC_DS08854,BMG_DS034235,extragonadal nonseminomatous germ cell tumor
+BMGC_DS08855,BMG_DS034237,malignant gastric granular cell tumor
+BMGC_DS08856,BMG_DS034238,growth hormone-producing pituitary gland carcinoma
+BMGC_DS08857,BMG_DS034239,malignant leptomeningeal tumor
+BMGC_DS08858,BMG_DS034241,malignant mediastinum hemangiopericytoma
+BMGC_DS08859,BMG_DS034243,malignant melanocytic peripheral nerve sheath tumor of mediastinum
+BMGC_DS08860,BMG_DS034244,malignant mixed epithelial stromal tumor of the kidney
+BMGC_DS08861,BMG_DS034245,carcinosarcoma
+BMGC_DS08862,BMG_DS034247,perivascular tumor
+BMGC_DS08863,BMG_DS034248,malignant pineal area germ cell neoplasm
+BMGC_DS08864,BMG_DS034249,prolactin-producing pituitary gland carcinoma
+BMGC_DS08865,BMG_DS034250,malignant prostate phyllodes tumor
+BMGC_DS08866,BMG_DS034251,vascular cancer
+BMGC_DS08867,BMG_DS034252,vascular cancer
+BMGC_DS08868,BMG_DS034254,skeletal muscle cancer
+BMGC_DS08869,BMG_DS034255,smooth muscle cancer
+BMGC_DS08870,BMG_DS034256,synovium cancer
+BMGC_DS08871,BMG_DS034257,testicular non-seminomatous germ cell cancer
+BMGC_DS08872,BMG_DS034258,malignant thyroid stimulating hormone producing neoplasm of pituitary gland
+BMGC_DS08873,BMG_DS034259,uterine body mixed cancer
+BMGC_DS08874,BMG_DS034260,vascular cancer
+BMGC_DS08875,BMG_DS034261,breast intraductal proliferative lesion
+BMGC_DS08876,BMG_DS034262,neoplasm of mature B-cells
+BMGC_DS08877,BMG_DS034263,mature gastric teratoma
+BMGC_DS08878,BMG_DS034264,mature ovarian teratoma
+BMGC_DS08879,BMG_DS034267,maxillary sinus adenocarcinoma
+BMGC_DS08880,BMG_DS034268,maxillary sinus adenoid cystic carcinoma
+BMGC_DS08881,BMG_DS034269,maxillary sinus cholesteatoma
+BMGC_DS08882,BMG_DS034270,maxillary sinus inverted papilloma
+BMGC_DS08883,BMG_DS034271,maxillary sinus Schneiderian papilloma
+BMGC_DS08884,BMG_DS034272,maxillary sinus squamous cell carcinoma
+BMGC_DS08885,BMG_DS034273,mediastinum angiosarcoma
+BMGC_DS08886,BMG_DS034274,mediastinum ganglioneuroblastoma
+BMGC_DS08887,BMG_DS034275,mediastinal germ cell tumor
+BMGC_DS08888,BMG_DS034276,mediastinal granular cell myoblastoma
+BMGC_DS08889,BMG_DS034277,mediastinal gray zone lymphoma
+BMGC_DS08890,BMG_DS034279,mediastinum leiomyosarcoma
+BMGC_DS08891,BMG_DS034280,mediastinal lipomatosis
+BMGC_DS08892,BMG_DS034281,mediastinum liposarcoma
+BMGC_DS08893,BMG_DS034282,mediastinal malignant lymphoma
+BMGC_DS08894,BMG_DS034283,mediastinal melanocytic neurilemmoma
+BMGC_DS08895,BMG_DS034284,mediastinal mesenchymal tumor
+BMGC_DS08896,BMG_DS034285,mediastinal neural neoplasm
+BMGC_DS08897,BMG_DS034286,mediastinum neuroblastoma
+BMGC_DS08898,BMG_DS034287,mediastinum neurofibroma
+BMGC_DS08899,BMG_DS034288,mediastinal extraskeletal osteosarcoma
+BMGC_DS08900,BMG_DS034289,mediastinum rhabdomyosarcoma
+BMGC_DS08901,BMG_DS034290,mediastinum sarcoma
+BMGC_DS08902,BMG_DS034291,mediastinal schwannoma
+BMGC_DS08903,BMG_DS034292,mediastinum seminoma
+BMGC_DS08904,BMG_DS034293,mediastinum synovial sarcoma
+BMGC_DS08905,BMG_DS034294,mediastinum teratoma
+BMGC_DS08906,BMG_DS034296,melanomatosis
+BMGC_DS08907,BMG_DS034297,meningioma | supratentorial meningioma
+BMGC_DS08908,BMG_DS034298,mesenchymal cell neoplasm
+BMGC_DS08909,BMG_DS034299,metachronous osteosarcoma of the bone
+BMGC_DS08910,BMG_DS034300,metachronous kidney Wilms' tumor
+BMGC_DS08911,BMG_DS034301,metaplastic breast carcinoma
+BMGC_DS08912,BMG_DS034302,metastatic carcinoma in the adrenal medulla
+BMGC_DS08913,BMG_DS034303,methotrexate-associated lymphoproliferative disorders
+BMGC_DS08914,BMG_DS034304,microglandular adenosis of breast
+BMGC_DS08915,BMG_DS034305,middle cranial fossa meningioma
+BMGC_DS08916,BMG_DS034306,middle ear adenocarcinoma
+BMGC_DS08917,BMG_DS034308,middle ear carcinoma
+BMGC_DS08918,BMG_DS034309,middle ear squamous cell carcinoma
+BMGC_DS08919,BMG_DS034313,mixed cell uveal melanoma
+BMGC_DS08920,BMG_DS034314,mixed hepatoblastoma
+BMGC_DS08921,BMG_DS034316,lung mixed small cell and squamous cell carcinoma
+BMGC_DS08922,BMG_DS034317,monophasic synovial sarcoma
+BMGC_DS08923,BMG_DS034318,breast mucinous carcinoma
+BMGC_DS08924,BMG_DS034319,mucinous gastric adenocarcinoma
+BMGC_DS08925,BMG_DS034321,mucoepidermoid breast carcinoma
+BMGC_DS08926,BMG_DS034322,thymic mucoepidermoid carcinoma
+BMGC_DS08927,BMG_DS034323,multicentric Castleman disease
+BMGC_DS08928,BMG_DS034324,multicentric papillary thyroid carcinoma
+BMGC_DS08929,BMG_DS034326,multifocal osteogenic sarcoma
+BMGC_DS08930,BMG_DS034327,multiple spinal canal and spinal cord meningioma
+BMGC_DS08931,BMG_DS034328,multiple mucosal neuroma
+BMGC_DS08932,BMG_DS034329,multiple skull base meningioma
+BMGC_DS08933,BMG_DS034330,nasal cavity adenocarcinoma
+BMGC_DS08934,BMG_DS034331,nasal cavity lymphoma
+BMGC_DS08935,BMG_DS034332,nasal cavity olfactory neuroblastoma
+BMGC_DS08936,BMG_DS034334,head and neck carcinoma
+BMGC_DS08937,BMG_DS034336,nerve plexus neoplasm
+BMGC_DS08938,BMG_DS034337,nerve root neoplasm
+BMGC_DS08939,BMG_DS034339,nervous system cancer
+BMGC_DS08940,BMG_DS034340,posterior pituitary gland neoplasm
+BMGC_DS08941,BMG_DS034341,nipple carcinoma
+BMGC_DS08942,BMG_DS034342,nipple duct carcinoma
+BMGC_DS08943,BMG_DS034345,medulloblastoma with extensive nodularity
+BMGC_DS08944,BMG_DS034347,non-functional pancreatic neuroendocrine tumor
+BMGC_DS08945,BMG_DS034348,non-invasive verrucous carcinoma of the penis
+BMGC_DS08946,BMG_DS034349,peripheral nervous system disease
+BMGC_DS08947,BMG_DS034350,reproductive system disease
+BMGC_DS08948,BMG_DS034351,urinary system disease
+BMGC_DS08949,BMG_DS034353,lung adenocarcinoma
+BMGC_DS08950,BMG_DS034354,non specific chronic endometritis
+BMGC_DS08951,BMG_DS034355,nonanaplastic kidney Wilms tumor
+BMGC_DS08952,BMG_DS034356,non-ossifying fibromyxoid tumor
+BMGC_DS08953,BMG_DS034357,notochordal tumor
+BMGC_DS08954,BMG_DS034358,lung occult large cell carcinoma
+BMGC_DS08955,BMG_DS034359,lung occult adenocarcinoma
+BMGC_DS08956,BMG_DS034360,occult small cell lung carcinoma
+BMGC_DS08957,BMG_DS034361,lung occult squamous cell carcinoma
+BMGC_DS08958,BMG_DS034362,olfactory groove meningioma
+BMGC_DS08959,BMG_DS034364,optic nerve astrocytoma
+BMGC_DS08960,BMG_DS034365,orbit alveolar rhabdomyosarcoma
+BMGC_DS08961,BMG_DS034366,orbit embryonal rhabdomyosarcoma
+BMGC_DS08962,BMG_DS034367,hemangioma of orbit
+BMGC_DS08963,BMG_DS034368,orbit sarcoma
+BMGC_DS08964,BMG_DS034371,breast extraskeletal osteosarcoma
+BMGC_DS08965,BMG_DS034373,ovarian angiosarcoma
+BMGC_DS08966,BMG_DS034374,ovarian cystic teratoma
+BMGC_DS08967,BMG_DS034376,ovarian endometrial cancer
+BMGC_DS08968,BMG_DS034377,ovary leiomyosarcoma
+BMGC_DS08969,BMG_DS034378,liposarcoma of the ovary
+BMGC_DS08970,BMG_DS034379,ovarian mucinous adenocarcinoma
+BMGC_DS08971,BMG_DS034380,ovarian mucinous neoplasm
+BMGC_DS08972,BMG_DS034381,ovarian adenosarcoma
+BMGC_DS08973,BMG_DS034382,ovarian myxoid liposarcoma
+BMGC_DS08974,BMG_DS034383,ovarian neuroendocrine neoplasm
+BMGC_DS08975,BMG_DS034384,ovarian large-cell neuroendocrine carcinoma
+BMGC_DS08976,BMG_DS034385,ovarian papillary cystadenoma
+BMGC_DS08977,BMG_DS034386,ovary rhabdomyosarcoma
+BMGC_DS08978,BMG_DS034387,ovarian serous adenocarcinoma
+BMGC_DS08979,BMG_DS034388,ovarian serous surface papillary adenocarcinoma
+BMGC_DS08980,BMG_DS034389,ovarian solid teratoma
+BMGC_DS08981,BMG_DS034390,ovarian surface papilloma
+BMGC_DS08982,BMG_DS034391,ovarian transitional cell carcinoma
+BMGC_DS08983,BMG_DS034393,pancreatic adenosquamous carcinoma
+BMGC_DS08984,BMG_DS034394,pancreatic ACTH-producing neuroendocrine tumor
+BMGC_DS08985,BMG_DS034395,pancreatic delta cell neuroendocrine tumor
+BMGC_DS08986,BMG_DS034396,pancreatic ductal adenocarcinoma
+BMGC_DS08987,BMG_DS034397,pancreatic foamy gland adenocarcinoma
+BMGC_DS08988,BMG_DS034398,pancreatic intraductal papillary-mucinous carcinoma
+BMGC_DS08989,BMG_DS034399,pancreas lymphoma
+BMGC_DS08990,BMG_DS034400,pancreatic mucinous cystadenoma
+BMGC_DS08991,BMG_DS034401,pancreatic mucinous ductal ectasia
+BMGC_DS08992,BMG_DS034402,pancreatic non-functioning delta cell tumor
+BMGC_DS08993,BMG_DS034403,pancreatic serous cystadenocarcinoma
+BMGC_DS08994,BMG_DS034404,pancreatic serous cystadenoma
+BMGC_DS08995,BMG_DS034405,pancreatic signet ring cell adenocarcinoma
+BMGC_DS08996,BMG_DS034406,papillary carcinoma of the penis
+BMGC_DS08997,BMG_DS034408,papillary lung adenocarcinoma
+BMGC_DS08998,BMG_DS034409,papillary thymic adenocarcinoma
+BMGC_DS08999,BMG_DS034411,papillary urothelial neoplasm
+BMGC_DS09000,BMG_DS034412,paranasal sinus cancer
+BMGC_DS09001,BMG_DS034413,paranasal sinus adenoid cystic carcinoma
+BMGC_DS09002,BMG_DS034414,paranasal sinus lymphoma
+BMGC_DS09003,BMG_DS034415,paranasal sinus mucoepidermoid carcinoma
+BMGC_DS09004,BMG_DS034416,paranasal sinus sarcoma
+BMGC_DS09005,BMG_DS034418,paratesticular lipoma
+BMGC_DS09006,BMG_DS034420,parathyroid oncocytic adenoma
+BMGC_DS09007,BMG_DS034421,Skene gland carcinoma
+BMGC_DS09008,BMG_DS034427,Kaposi's sarcoma
+BMGC_DS09009,BMG_DS034428,periampullary adenocarcinoma
+BMGC_DS09010,BMG_DS034430,malignant pericardial mesothelioma
+BMGC_DS09011,BMG_DS034432,periocular meningioma
+BMGC_DS09012,BMG_DS034433,peripheral ganglioneuroblastoma
+BMGC_DS09013,BMG_DS034434,microscopic breast papilloma
+BMGC_DS09014,BMG_DS034435,pericytic neoplasm
+BMGC_DS09015,BMG_DS034436,petroclival meningioma
+BMGC_DS09016,BMG_DS034437,petrous apex meningioma
+BMGC_DS09017,BMG_DS034442,pineal region choriocarcinoma
+BMGC_DS09018,BMG_DS034443,pineal region dysgerminoma
+BMGC_DS09019,BMG_DS034444,pineal region immature teratoma
+BMGC_DS09020,BMG_DS034445,pineal region mature teratoma
+BMGC_DS09021,BMG_DS034446,pineal region meningioma
+BMGC_DS09022,BMG_DS034447,pineal region teratoma
+BMGC_DS09023,BMG_DS034448,pineal region yolk sac tumor
+BMGC_DS09024,BMG_DS034449,pituitary stalk meningioma
+BMGC_DS09025,BMG_DS034450,placenta disease
+BMGC_DS09026,BMG_DS034452,neurilemmoma of the pleura
+BMGC_DS09027,BMG_DS034453,plexopathy
+BMGC_DS09028,BMG_DS034454,posterior foramen magnum meningioma
+BMGC_DS09029,BMG_DS034455,precursor lymphoblastic lymphoma/leukemia
+BMGC_DS09030,BMG_DS034457,chondrosarcoma
+BMGC_DS09031,BMG_DS034459,primary skin meningioma
+BMGC_DS09032,BMG_DS034461,lung meningioma
+BMGC_DS09033,BMG_DS034462,prostate adenoid cystic carcinoma
+BMGC_DS09034,BMG_DS034463,adenosquamous prostate carcinoma
+BMGC_DS09035,BMG_DS034464,prostate angiosarcoma
+BMGC_DS09036,BMG_DS034465,prostate embryonal rhabdomyosarcoma
+BMGC_DS09037,BMG_DS034466,Kaposi's sarcoma
+BMGC_DS09038,BMG_DS034468,prostate leiomyosarcoma
+BMGC_DS09039,BMG_DS034469,prostate lymphoma
+BMGC_DS09040,BMG_DS034470,acinar prostate mucinous adenocarcinoma
+BMGC_DS09041,BMG_DS034471,prostate neuroendocrine neoplasm
+BMGC_DS09042,BMG_DS034472,prostate rhabdomyosarcoma
+BMGC_DS09043,BMG_DS034473,prostate signet ring cell adenocarcinoma
+BMGC_DS09044,BMG_DS034474,prostate stromal sarcoma
+BMGC_DS09045,BMG_DS034475,proximal-type epithelioid sarcoma
+BMGC_DS09046,BMG_DS034477,pulmonary artery leiomyosarcoma
+BMGC_DS09047,BMG_DS034478,pulmonary sulcus neoplasm
+BMGC_DS09048,BMG_DS034479,pulmonary vein leiomyosarcoma
+BMGC_DS09049,BMG_DS034480,reactive cutaneous fibrous lesion
+BMGC_DS09050,BMG_DS034483,rectum Kaposi sarcoma
+BMGC_DS09051,BMG_DS034484,rectum leiomyoma
+BMGC_DS09052,BMG_DS034485,rectum leiomyosarcoma
+BMGC_DS09053,BMG_DS034486,lipoma of the rectum
+BMGC_DS09054,BMG_DS034487,rectum lymphoma
+BMGC_DS09055,BMG_DS034488,rectum neuroendocrine neoplasm
+BMGC_DS09056,BMG_DS034489,rectum rhabdomyosarcoma
+BMGC_DS09057,BMG_DS034490,rectum sarcoma
+BMGC_DS09058,BMG_DS034491,rectal sarcomatoid carcinoma
+BMGC_DS09059,BMG_DS034492,squamous cell carcinoma of rectum
+BMGC_DS09060,BMG_DS034494,refractory hematologic cancer
+BMGC_DS09061,BMG_DS034495,kidney leiomyosarcoma
+BMGC_DS09062,BMG_DS034496,kidney lipoma
+BMGC_DS09063,BMG_DS034497,kidney liposarcoma
+BMGC_DS09064,BMG_DS034498,kidney osteogenic sarcoma
+BMGC_DS09065,BMG_DS034499,renal pelvis adenocarcinoma
+BMGC_DS09066,BMG_DS034500,renal pelvis carcinoma
+BMGC_DS09067,BMG_DS034501,renal pelvis inverted papilloma
+BMGC_DS09068,BMG_DS034502,kidney pelvis sarcomatoid transitional cell carcinoma
+BMGC_DS09069,BMG_DS034503,vascular cancer
+BMGC_DS09070,BMG_DS034504,retinal cell neoplasm
+BMGC_DS09071,BMG_DS034505,retroperitoneal germ cell neoplasm
+BMGC_DS09072,BMG_DS034506,retroperitoneal hemangiopericytoma
+BMGC_DS09073,BMG_DS034507,retroperitoneal lymphoma
+BMGC_DS09074,BMG_DS034508,sacral spinal canal and spinal cord meningioma
+BMGC_DS09075,BMG_DS034512,sarcomatoid penile squamous cell carcinoma
+BMGC_DS09076,BMG_DS034513,thymic sarcomatoid carcinoma
+BMGC_DS09077,BMG_DS034514,schwannoma of twelfth cranial nerve
+BMGC_DS09078,BMG_DS034515,schwannomatosis
+BMGC_DS09079,BMG_DS034516,sclerosing adenosis of breast
+BMGC_DS09080,BMG_DS034517,sclerosing breast papilloma
+BMGC_DS09081,BMG_DS034518,scrotum basal cell carcinoma
+BMGC_DS09082,BMG_DS034519,scrotal hemangioma
+BMGC_DS09083,BMG_DS034520,selective immunoglobulin deficiency disease
+BMGC_DS09084,BMG_DS034522,signet ring cell breast carcinoma
+BMGC_DS09085,BMG_DS034523,signet ring cell gastric adenocarcinoma
+BMGC_DS09086,BMG_DS034524,skeletal muscle neoplasm
+BMGC_DS09087,BMG_DS034525,skin basaloid carcinoma
+BMGC_DS09088,BMG_DS034526,pseudovascular skin squamous cell carcinoma
+BMGC_DS09089,BMG_DS034527,skull base chordoma
+BMGC_DS09090,BMG_DS034528,skull base meningioma
+BMGC_DS09091,BMG_DS034529,extrahepatic bile duct small cell adenocarcinoma
+BMGC_DS09092,BMG_DS034530,thymus small cell carcinoma
+BMGC_DS09093,BMG_DS034534,small intestinal fibrosarcoma
+BMGC_DS09094,BMG_DS034537,small intestine neuroendocrine neoplasm
+BMGC_DS09095,BMG_DS034538,small intestinal sarcoma
+BMGC_DS09096,BMG_DS034539,small intestinal vasoactive intestinal peptide producing tumor
+BMGC_DS09097,BMG_DS034540,fibrosarcoma
+BMGC_DS09098,BMG_DS034541,solid papillary breast carcinoma
+BMGC_DS09099,BMG_DS034542,solid pseudopapillary carcinoma of pancreas
+BMGC_DS09100,BMG_DS034544,sphenocavernous meningioma
+BMGC_DS09101,BMG_DS034545,sphenoid sinus inverted papilloma
+BMGC_DS09102,BMG_DS034546,sphenoid sinus Schneiderian papilloma
+BMGC_DS09103,BMG_DS034547,sphenoid sinus squamous cell carcinoma
+BMGC_DS09104,BMG_DS034548,sphenoorbital meningioma
+BMGC_DS09105,BMG_DS034549,spinal cord lymphoma
+BMGC_DS09106,BMG_DS034550,spinal cord melanoma
+BMGC_DS09107,BMG_DS034551,spinal cord neuroblastoma
+BMGC_DS09108,BMG_DS034552,neurofibroma of spinal cord
+BMGC_DS09109,BMG_DS034553,spinal cord primitive neuroectodermal tumor
+BMGC_DS09110,BMG_DS034554,spinal cord sarcoma
+BMGC_DS09111,BMG_DS034555,spinal multifocal clear cell meningioma
+BMGC_DS09112,BMG_DS034557,splenic manifestation of hairy cell leukemia
+BMGC_DS09113,BMG_DS034558,splenic manifestation of leukemia
+BMGC_DS09114,BMG_DS034559,splenic manifestation of prolymphocytic leukemia
+BMGC_DS09115,BMG_DS034560,sporadic breast cancer
+BMGC_DS09116,BMG_DS034561,papillary renal cell carcinoma
+BMGC_DS09117,BMG_DS034562,squamous cell breast carcinoma
+BMGC_DS09118,BMG_DS034563,penis squamous cell carcinoma
+BMGC_DS09119,BMG_DS034564,thymus squamous cell carcinoma
+BMGC_DS09120,BMG_DS034566,intratubular embryonal carcinoma
+BMGC_DS09121,BMG_DS034567,stage IVb bladder cancer
+BMGC_DS09122,BMG_DS034568,sternum lymphoma
+BMGC_DS09123,BMG_DS034569,steroid lipomatosis
+BMGC_DS09124,BMG_DS034574,superficial urinary bladder carcinoma
+BMGC_DS09125,BMG_DS034575,lung superior sulcus carcinoma
+BMGC_DS09126,BMG_DS034576,superior vena cava angiosarcoma
+BMGC_DS09127,BMG_DS034577,superior vena cava leiomyosarcoma
+BMGC_DS09128,BMG_DS034578,suprasellar meningioma
+BMGC_DS09129,BMG_DS034580,supratentorial primitive neuroectodermal tumor
+BMGC_DS09130,BMG_DS034581,sympathetic neurilemmoma
+BMGC_DS09131,BMG_DS034582,synchronous multifocal osteogenic sarcoma
+BMGC_DS09132,BMG_DS034583,synovial angioma
+BMGC_DS09133,BMG_DS034585,tall cell variant thyroid gland papillary carcinoma
+BMGC_DS09134,BMG_DS034586,telangiectatic glomangioma
+BMGC_DS09135,BMG_DS034587,tendon sheath lipoma
+BMGC_DS09136,BMG_DS034588,testicular germ cell tumor
+BMGC_DS09137,BMG_DS034589,testicular granulosa cell tumor
+BMGC_DS09138,BMG_DS034590,testicular leukemia
+BMGC_DS09139,BMG_DS034591,mixed testicular germ cell cancer
+BMGC_DS09140,BMG_DS034592,testis rhabdomyosarcoma
+BMGC_DS09141,BMG_DS034593,testis sarcoma
+BMGC_DS09142,BMG_DS034594,thalamic neoplasm
+BMGC_DS09143,BMG_DS034595,thoracic spinal canal and spinal cord meningioma
+BMGC_DS09144,BMG_DS034596,thymus gland adenocarcinoma
+BMGC_DS09145,BMG_DS034598,thymus lymphoma
+BMGC_DS09146,BMG_DS034599,thyroid gland angiosarcoma
+BMGC_DS09147,BMG_DS034601,thyroid gland oncocytic adenoma
+BMGC_DS09148,BMG_DS034602,thyroid hyalinizing trabecular adenoma
+BMGC_DS09149,BMG_DS034603,thyroid lymphoma
+BMGC_DS09150,BMG_DS034605,thyroid sarcoma
+BMGC_DS09151,BMG_DS034609,tracheal lymphoma
+BMGC_DS09152,BMG_DS034610,trachea sarcoma
+BMGC_DS09153,BMG_DS034611,tuberculum sellae meningioma
+BMGC_DS09154,BMG_DS034615,upper clivus meningioma
+BMGC_DS09155,BMG_DS034616,ureter adenocarcinoma
+BMGC_DS09156,BMG_DS034617,ureter inverted papilloma
+BMGC_DS09157,BMG_DS034618,ureter leiomyoma
+BMGC_DS09158,BMG_DS034619,ureteral lymphoma
+BMGC_DS09159,BMG_DS034620,schwannoma of ureter
+BMGC_DS09160,BMG_DS034621,ureter small cell carcinoma
+BMGC_DS09161,BMG_DS034622,ureter squamous cell carcinoma
+BMGC_DS09162,BMG_DS034623,fibroepithelial polyp of urethra
+BMGC_DS09163,BMG_DS034624,urethra adenocarcinoma
+BMGC_DS09164,BMG_DS034625,urethra clear cell adenocarcinoma
+BMGC_DS09165,BMG_DS034626,urethra inverted papilloma
+BMGC_DS09166,BMG_DS034627,urethra leiomyoma
+BMGC_DS09167,BMG_DS034628,nephrogenic adenoma of the urethra
+BMGC_DS09168,BMG_DS034629,urethra squamous cell carcinoma
+BMGC_DS09169,BMG_DS034637,adenomyoma of uterine corpus
+BMGC_DS09170,BMG_DS034638,uterine corpus choriocarcinoma
+BMGC_DS09171,BMG_DS034639,endometrial endometrioid adenocarcinoma
+BMGC_DS09172,BMG_DS034640,endometrial endometrioid adenocarcinoma with spindled epithelial cells
+BMGC_DS09173,BMG_DS034641,uterine corpus adenosarcoma
+BMGC_DS09174,BMG_DS034643,vagina leiomyosarcoma
+BMGC_DS09175,BMG_DS034645,vaginal yolk sac tumor
+BMGC_DS09176,BMG_DS034647,penis verrucous carcinoma
+BMGC_DS09177,BMG_DS034648,villoglandular endometrial endometrioid adenocarcinoma
+BMGC_DS09178,BMG_DS034649,optic tract astrocytoma
+BMGC_DS09179,BMG_DS034651,vulvar adenocarcinoma
+BMGC_DS09180,BMG_DS034652,vulva basal cell carcinoma
+BMGC_DS09181,BMG_DS034653,vulva fibroepithelial polyp
+BMGC_DS09182,BMG_DS034654,vulvar seborrheic keratosis
+BMGC_DS09183,BMG_DS034655,vestibular papilloma
+BMGC_DS09184,BMG_DS034656,vulva verrucous carcinoma
+BMGC_DS09185,BMG_DS034659,well differentiated papillary mesothelioma
+BMGC_DS09186,BMG_DS034660,differentiated thyroid carcinoma
+BMGC_DS09187,BMG_DS034661,Xanthogranulomatous cholecystitis
+BMGC_DS09188,BMG_DS034663,yolk sac tumor of central nervous system
+BMGC_DS09189,BMG_DS034665,Acute amebic dysentery without mention of abscess
+BMGC_DS09190,BMG_DS034670,cerebral cavernous malformation 1
+BMGC_DS09191,BMG_DS034671,kaposiform hemangioendothelioma
+BMGC_DS09192,BMG_DS034672,juvenile nasopharyngeal angiofibroma
+BMGC_DS09193,BMG_DS034673,marginal zone lymphoma
+BMGC_DS09194,BMG_DS034674,eccrine papillary adenocarcinoma
+BMGC_DS09195,BMG_DS034676,pineal parenchymal tumor of intermediate differentiation
+BMGC_DS09196,BMG_DS034679,Paget disease
+BMGC_DS09197,BMG_DS034680,Pulmonary insufficiency following trauma
+BMGC_DS09198,BMG_DS034681,Pulmonary insufficiency following shock
+BMGC_DS09199,BMG_DS034682,pancreatic somatostatinoma
+BMGC_DS09200,BMG_DS034683,pancreatic gastrin-producing neuroendocrine tumor
+BMGC_DS09201,BMG_DS034686,basal cell carcinoma
+BMGC_DS09202,BMG_DS034687,mixed neoplasm
+BMGC_DS09203,BMG_DS034689,epithelial neoplasm
+BMGC_DS09204,BMG_DS034691,sebaceous adenoma
+BMGC_DS09205,BMG_DS034692,childhood neoplasm
+BMGC_DS09206,BMG_DS034693,adult cystic teratoma
+BMGC_DS09207,BMG_DS034695,cystic teratoma
+BMGC_DS09208,BMG_DS034696,mature teratoma
+BMGC_DS09209,BMG_DS034697,primary peritoneal serous/papillary carcinoma
+BMGC_DS09210,BMG_DS034699,ovarian granulosa cell tumor
+BMGC_DS09211,BMG_DS034700,scrotal carcinoma
+BMGC_DS09212,BMG_DS034701,tanycytic ependymoma
+BMGC_DS09213,BMG_DS034702,adult central nervous system embryonal carcinoma
+BMGC_DS09214,BMG_DS034703,adult central nervous system germinoma
+BMGC_DS09215,BMG_DS034704,adult central nervous system choriocarcinoma
+BMGC_DS09216,BMG_DS034705,adult central nervous system teratoma
+BMGC_DS09217,BMG_DS034706,cerebellar liponeurocytoma
+BMGC_DS09218,BMG_DS034707,chordoid meningioma
+BMGC_DS09219,BMG_DS034708,perineurioma
+BMGC_DS09220,BMG_DS034709,intraneural perineurioma
+BMGC_DS09221,BMG_DS034710,plexiform schwannoma
+BMGC_DS09222,BMG_DS034711,clear cell hidradenoma
+BMGC_DS09223,BMG_DS034713,bile duct adenocarcinoma
+BMGC_DS09224,BMG_DS034714,Interstitial emphysema
+BMGC_DS09225,BMG_DS034715,well-differentiated liposarcoma
+BMGC_DS09226,BMG_DS034716,inflammatory liposarcoma
+BMGC_DS09227,BMG_DS034717,childhood germ cell brain tumor
+BMGC_DS09228,BMG_DS034718,pediatric CNS choriocarcinoma
+BMGC_DS09229,BMG_DS034719,childhood central nervous system embryonal carcinoma
+BMGC_DS09230,BMG_DS034721,central nervous system endodermal sinus tumor
+BMGC_DS09231,BMG_DS034723,nasal cavity carcinoma
+BMGC_DS09232,BMG_DS034724,periosteal osteogenic sarcoma
+BMGC_DS09233,BMG_DS034725,mucinous cystadenofibroma
+BMGC_DS09234,BMG_DS034726,papillary adenofibroma
+BMGC_DS09235,BMG_DS034727,clear cell cystadenofibroma
+BMGC_DS09236,BMG_DS034728,testis refractory cancer
+BMGC_DS09237,BMG_DS034731,pleural mesothelioma
+BMGC_DS09238,BMG_DS034732,adult brainstem gliosarcoma
+BMGC_DS09239,BMG_DS034733,adult brainstem mixed glioma
+BMGC_DS09240,BMG_DS034735,oncocytic neoplasm
+BMGC_DS09241,BMG_DS034737,acute leukemia
+BMGC_DS09242,BMG_DS034738,renal carcinoma
+BMGC_DS09243,BMG_DS034739,sternum cancer
+BMGC_DS09244,BMG_DS034740,sebaceous gland cancer
+BMGC_DS09245,BMG_DS034741,cellular ependymoma
+BMGC_DS09246,BMG_DS034742,secretory meningioma
+BMGC_DS09247,BMG_DS034743,microcystic meningioma
+BMGC_DS09248,BMG_DS034744,leptomeningeal sarcoma
+BMGC_DS09249,BMG_DS034748,Conn Syndrome
+BMGC_DS09250,BMG_DS034749,Primary testicular failure
+BMGC_DS09251,BMG_DS034750,Congenital absence of germinal epithelium of testes
+BMGC_DS09252,BMG_DS034753,Tinea cruris
+BMGC_DS09253,BMG_DS034756,Systemic onset juvenile chronic arthritis
+BMGC_DS09254,BMG_DS034759,Cervical spondylosis
+BMGC_DS09255,BMG_DS034760,hearing loss disorder
+BMGC_DS09256,BMG_DS034763,bladder urothelial papilloma
+BMGC_DS09257,BMG_DS034773,Cystic Disease Of Lung
+BMGC_DS09258,BMG_DS034789,Aneurysm Of Interventricular Septum
+BMGC_DS09259,BMG_DS034790,Angiostrongylus costaricensis infection
+BMGC_DS09260,BMG_DS034795,breast apocrine adenoma
+BMGC_DS09261,BMG_DS034799,atrioventricular septal defect
+BMGC_DS09262,BMG_DS034802,Peroneal muscle atrophy
+BMGC_DS09263,BMG_DS034819,Congenital cardiomyopathy
+BMGC_DS09264,BMG_DS034840,Intrinsic Factor Deficiency
+BMGC_DS09265,BMG_DS034847,polydactyly of a biphalangeal thumb
+BMGC_DS09266,BMG_DS034872,Ectopic rhythm
+BMGC_DS09267,BMG_DS034874,HEMIFACIAL HYPERPLASIA
+BMGC_DS09268,BMG_DS034912,Retinitis punctata albescens (disorder)
+BMGC_DS09269,BMG_DS034941,"incisors, shovel-shaped"
+BMGC_DS09270,BMG_DS034952,Mesenteric vascular insufficiency
+BMGC_DS09271,BMG_DS034954,pineal body neoplasm
+BMGC_DS09272,BMG_DS034956,sweat gland carcinoma
+BMGC_DS09273,BMG_DS034958,anal squamous cell carcinoma
+BMGC_DS09274,BMG_DS034959,anal margin squamous cell carcinoma
+BMGC_DS09275,BMG_DS034960,Paine syndrome
+BMGC_DS09276,BMG_DS034961,"DEAFNESS, AUTOSOMAL RECESSIVE 25"
+BMGC_DS09277,BMG_DS034962,"Dystonia 6, torsion"
+BMGC_DS09278,BMG_DS034964,"HETEROTAXY, VISCERAL, 2, AUTOSOMAL"
+BMGC_DS09279,BMG_DS034965,RETINITIS PIGMENTOSA 23
+BMGC_DS09280,BMG_DS034966,RETINITIS PIGMENTOSA 28
+BMGC_DS09281,BMG_DS034968,CONE-ROD DYSTROPHY 9
+BMGC_DS09282,BMG_DS034975,Solar dermatitis
+BMGC_DS09283,BMG_DS034977,Hypervitaminosis D
+BMGC_DS09284,BMG_DS034979,Lumbar Osteoarthritis
+BMGC_DS09285,BMG_DS034983,Exostoses
+BMGC_DS09286,BMG_DS034987,"Muscular Dystrophy, Cardiac Type"
+BMGC_DS09287,BMG_DS034988,"Chondrodysplasia Punctata, Autosomal Dominant"
+BMGC_DS09288,BMG_DS034992,Actinic porokeratosis
+BMGC_DS09289,BMG_DS034993,Avascular necrosis of the capital femoral epiphysis
+BMGC_DS09290,BMG_DS034995,Alcoholic liver damage
+BMGC_DS09291,BMG_DS034997,"Hyperglycinemia with ketosis and leukopenia, types I and II"
+BMGC_DS09292,BMG_DS035009,Carnitine Acetyltransferase Deficiency
+BMGC_DS09293,BMG_DS035035,Chronic Q Fever
+BMGC_DS09294,BMG_DS035049,Neomycin sulfate allergy
+BMGC_DS09295,BMG_DS035115,"Juvenile idiopathic arthritis, extended oligoarthritis"
+BMGC_DS09296,BMG_DS035128,"Cardiomyopathy, Familial Idiopathic"
+BMGC_DS09297,BMG_DS035129,CADASILM
+BMGC_DS09298,BMG_DS035130,Sphincter of Oddi Stenosis
+BMGC_DS09299,BMG_DS035131,Gallbladder Dyskinesia
+BMGC_DS09300,BMG_DS035132,Primary Peritonitis
+BMGC_DS09301,BMG_DS035133,Secondary Peritonitis
+BMGC_DS09302,BMG_DS035134,Endocrine Breast Diseases
+BMGC_DS09303,BMG_DS035135,Adolescent Gynecomastia
+BMGC_DS09304,BMG_DS035136,Infant Gynecomastia
+BMGC_DS09305,BMG_DS035139,"Pseudohypoaldosteronism, Type I, Autosomal Dominant"
+BMGC_DS09306,BMG_DS035140,"Pseudohypoaldosteronism, Type I, Autosomal Recessive"
+BMGC_DS09307,BMG_DS035141,"Pseudohypoaldosteronism, Type II"
+BMGC_DS09308,BMG_DS035142,Erythematotelangiectatic Rosacea
+BMGC_DS09309,BMG_DS035143,Papulopustular Rosacea
+BMGC_DS09310,BMG_DS035144,Phymatous Rosacea
+BMGC_DS09311,BMG_DS035145,Autosomal Recessive Emery-Dreifuss Muscular Dystrophy
+BMGC_DS09312,BMG_DS035146,Tibial Muscular Dystrophy
+BMGC_DS09313,BMG_DS035153,Acute fatty liver of pregnancy
+BMGC_DS09314,BMG_DS035160,Vagotonia
+BMGC_DS09315,BMG_DS035164,smooth surface dental caries
+BMGC_DS09316,BMG_DS035165,dentine erosion
+BMGC_DS09317,BMG_DS035166,pulp erosion
+BMGC_DS09318,BMG_DS035168,internal pathological resorption
+BMGC_DS09319,BMG_DS035179,Narcolepsy without cataplexy
+BMGC_DS09320,BMG_DS035181,Midline cystocele
+BMGC_DS09321,BMG_DS035182,perineocele
+BMGC_DS09322,BMG_DS035183,pelvic muscle wasting
+BMGC_DS09323,BMG_DS035187,non-renal secondary hyperparathyroidism
+BMGC_DS09324,BMG_DS035190,alcohol-induced mental disorder
+BMGC_DS09325,BMG_DS035200,Still's disease with juvenile onset and/or adult onset
+BMGC_DS09326,BMG_DS035202,Ureteral Calculi
+BMGC_DS09327,BMG_DS035204,Alpha plus thalassemia
+BMGC_DS09328,BMG_DS035207,Congenital hypogammaglobulinemia
+BMGC_DS09329,BMG_DS035212,breast neoplasm
+BMGC_DS09330,BMG_DS035218,Testotoxicosis
+BMGC_DS09331,BMG_DS035227,Stenosis of middle cerebral artery
+BMGC_DS09332,BMG_DS035228,partial chromosome Y deletion
+BMGC_DS09333,BMG_DS035229,histiocytoma
+BMGC_DS09334,BMG_DS035230,lung sclerosing hemangioma
+BMGC_DS09335,BMG_DS035232,osteosclerotic myeloma
+BMGC_DS09336,BMG_DS035233,Gait Apraxia
+BMGC_DS09337,BMG_DS035236,Entrapment Neuropathies
+BMGC_DS09338,BMG_DS035237,Chronic Actinic Dermatitis
+BMGC_DS09339,BMG_DS035240,acrocephalosyndactyly
+BMGC_DS09340,BMG_DS035241,Orofaciodigital Syndrome I
+BMGC_DS09341,BMG_DS035242,Vitamin Deficiency
+BMGC_DS09342,BMG_DS035243,drug dependence
+BMGC_DS09343,BMG_DS035244,Diverticulosis
+BMGC_DS09344,BMG_DS035245,Neuralgic Amyotrophy
+BMGC_DS09345,BMG_DS035246,"Cerebral Amyloid Angiopathy, Hereditary"
+BMGC_DS09346,BMG_DS035247,oncocytic adenoma
+BMGC_DS09347,BMG_DS035250,autism spectrum disorder
+BMGC_DS09348,BMG_DS035251,Absolute anemia
+BMGC_DS09349,BMG_DS035252,adenocarcinofibroma
+BMGC_DS09350,BMG_DS035253,epididymal adenocarcinoma
+BMGC_DS09351,BMG_DS035255,breast adenomyoepithelioma
+BMGC_DS09352,BMG_DS035256,adenosquamous breast carcinoma
+BMGC_DS09353,BMG_DS035257,atypical neurofibroma
+BMGC_DS09354,BMG_DS035258,Bartholin gland adenoid cystic carcinoma
+BMGC_DS09355,BMG_DS035259,Bartholin gland adenoma
+BMGC_DS09356,BMG_DS035260,Bartholin gland adenomyoma
+BMGC_DS09357,BMG_DS035261,Bartholin gland adenosquamous carcinoma
+BMGC_DS09358,BMG_DS035262,Bartholin gland small cell carcinoma
+BMGC_DS09359,BMG_DS035263,bartholin gland squamous cell carcinoma
+BMGC_DS09360,BMG_DS035264,Bartholin gland transitional cell carcinoma
+BMGC_DS09361,BMG_DS035265,cervical basaloid carcinoma
+BMGC_DS09362,BMG_DS035267,benign mixed tumor of the vulva
+BMGC_DS09363,BMG_DS035269,benign vaginal mixed epithelial and mesenchymal neoplasm
+BMGC_DS09364,BMG_DS035270,benign vaginal mixed tumor
+BMGC_DS09365,BMG_DS035271,bladder diffuse clear cell adenocarcinoma
+BMGC_DS09366,BMG_DS035272,bladder colonic type adenocarcinoma
+BMGC_DS09367,BMG_DS035273,bladder hepatoid adenocarcinoma
+BMGC_DS09368,BMG_DS035275,bladder mixed adenocarcinoma
+BMGC_DS09369,BMG_DS035276,bladder colloid adenocarcinoma
+BMGC_DS09370,BMG_DS035277,bladder papillary clear cell adenocarcinoma
+BMGC_DS09371,BMG_DS035278,bladder papillary urothelial neoplasm
+BMGC_DS09372,BMG_DS035280,bladder tubulo-cystic clear cell adenocarcinoma
+BMGC_DS09373,BMG_DS035281,bladder urachal adenocarcinoma
+BMGC_DS09374,BMG_DS035282,bladder urachal squamous cell carcinoma
+BMGC_DS09375,BMG_DS035283,bladder urachal urothelial carcinoma
+BMGC_DS09376,BMG_DS035284,bladder verrucous carcinoma
+BMGC_DS09377,BMG_DS035285,botryoid-type embryonal rhabdomyosarcoma of the vagina
+BMGC_DS09378,BMG_DS035286,breast adenomyoepithelial adenosis
+BMGC_DS09379,BMG_DS035287,breast angiomatosis
+BMGC_DS09380,BMG_DS035288,breast columnar cell mucinous carcinoma
+BMGC_DS09381,BMG_DS035290,breast ductal adenoma
+BMGC_DS09382,BMG_DS035292,breast granular cell tumor
+BMGC_DS09383,BMG_DS035293,breast hemangiopericytoma
+BMGC_DS09384,BMG_DS035294,breast large cell neuroendocrine carcinoma
+BMGC_DS09385,BMG_DS035296,breast mucinous cystadenocarcinoma
+BMGC_DS09386,BMG_DS035297,breast myoepithelial tumor
+BMGC_DS09387,BMG_DS035299,bulbomembranous urethral cancer
+BMGC_DS09388,BMG_DS035300,differentiating neuroblastoma
+BMGC_DS09389,BMG_DS035303,hereditary fallopian tube carcinoma
+BMGC_DS09390,BMG_DS035304,familial melanoma
+BMGC_DS09391,BMG_DS035306,chronic lymphoproliferative disorder of NK-cells
+BMGC_DS09392,BMG_DS035307,infiltrating bladder lymphoepithelioma-like carcinoma
+BMGC_DS09393,BMG_DS035308,"infiltrating bladder urothelial carcinoma, clear cell variant"
+BMGC_DS09394,BMG_DS035309,lipid-cell variant infiltrating bladder urothelial carcinoma
+BMGC_DS09395,BMG_DS035310,lymphoma-like variant infiltrating bladder urothelial carcinoma
+BMGC_DS09396,BMG_DS035311,microcystic variant infiltrating bladder urothelial carcinoma
+BMGC_DS09397,BMG_DS035312,nested variant infiltrating bladder urothelial carcinoma
+BMGC_DS09398,BMG_DS035313,plasmacytoid variant infiltrating bladder urothelial carcinoma
+BMGC_DS09399,BMG_DS035314,infiltrating bladder urothelial carcinoma sarcomatoid variant
+BMGC_DS09400,BMG_DS035315,infiltrating renal pelvis/ureter urothelial carcinoma
+BMGC_DS09401,BMG_DS035317,inner ear neoplasm
+BMGC_DS09402,BMG_DS035318,intraductal breast myoepitheliosis
+BMGC_DS09403,BMG_DS035319,malignant vaginal mixed epithelial and mesenchymal neoplasm
+BMGC_DS09404,BMG_DS035321,mixed endometrial stromal and smooth muscle tumor
+BMGC_DS09405,BMG_DS035322,mixed epithelial/mesenchymal metaplastic breast carcinoma
+BMGC_DS09406,BMG_DS035323,penis mixed squamous cell carcinoma
+BMGC_DS09407,BMG_DS035324,mucin-rich endometrial endometrioid adenocarcinoma
+BMGC_DS09408,BMG_DS035325,mucinous intrahepatic cholangiocarcinoma
+BMGC_DS09409,BMG_DS035326,mucinous tubular and spindle renal cell carcinoma
+BMGC_DS09410,BMG_DS035327,thyroid gland mucoepidermoid carcinoma
+BMGC_DS09411,BMG_DS035329,breast myoepitheliosis
+BMGC_DS09412,BMG_DS035331,polyembryoma of the ovary
+BMGC_DS09413,BMG_DS035332,testis polyembryoma
+BMGC_DS09414,BMG_DS035333,potassium deficiency disease
+BMGC_DS09415,BMG_DS035334,glioblastoma
+BMGC_DS09416,BMG_DS035335,primary peritoneal carcinoma
+BMGC_DS09417,BMG_DS035336,primary peritoneal serous adenocarcinoma
+BMGC_DS09418,BMG_DS035339,prostatic urethra urothelial carcinoma
+BMGC_DS09419,BMG_DS035340,prostatic urethral cancer
+BMGC_DS09420,BMG_DS035341,testicular pure germ cell tumor
+BMGC_DS09421,BMG_DS035342,renal pelvis urothelial papilloma
+BMGC_DS09422,BMG_DS035343,rete ovarii adenoma
+BMGC_DS09423,BMG_DS035344,rete ovarii cystadenofibroma
+BMGC_DS09424,BMG_DS035345,rete ovarii cystadenoma
+BMGC_DS09425,BMG_DS035346,rete ovarii neoplasm
+BMGC_DS09426,BMG_DS035348,rete testis neoplasm
+BMGC_DS09427,BMG_DS035350,submucosal invasive colon adenocarcinoma
+BMGC_DS09428,BMG_DS035351,synchronous bilateral breast carcinoma
+BMGC_DS09429,BMG_DS035352,tamoxifen-related endometrial lesion
+BMGC_DS09430,BMG_DS035353,testicular Brenner tumor
+BMGC_DS09431,BMG_DS035356,adult type testicular granulosa cell tumor
+BMGC_DS09432,BMG_DS035357,juvenile type testicular granulosa cell tumor
+BMGC_DS09433,BMG_DS035358,malignant testicular Leydig cell tumor
+BMGC_DS09434,BMG_DS035359,testicular sex cord-stromal neoplasm
+BMGC_DS09435,BMG_DS035360,testicular monophasic choriocarcinoma
+BMGC_DS09436,BMG_DS035361,cribriform variant testicular seminoma
+BMGC_DS09437,BMG_DS035362,pseudoglandular variant testicular seminoma
+BMGC_DS09438,BMG_DS035363,tubular variant testicular seminoma
+BMGC_DS09439,BMG_DS035365,testicular trophoblastic tumor
+BMGC_DS09440,BMG_DS035366,"testicular yolk sac tumor, endodermal sinus pattern"
+BMGC_DS09441,BMG_DS035367,enteric pattern testicular yolk sac tumor
+BMGC_DS09442,BMG_DS035368,"testicular yolk sac tumor, glandular-alveolar pattern"
+BMGC_DS09443,BMG_DS035369,"testicular yolk sac tumor, hepatoid pattern"
+BMGC_DS09444,BMG_DS035370,"testicular yolk sac tumor, macrocystic pattern"
+BMGC_DS09445,BMG_DS035371,reticular pattern testicular yolk sac tumor
+BMGC_DS09446,BMG_DS035372,"testicular yolk sac tumor, myxomatous pattern"
+BMGC_DS09447,BMG_DS035373,"testicular yolk sac tumor, papillary pattern"
+BMGC_DS09448,BMG_DS035374,polyvesicular vitelline pattern testicular yolk sac tumor
+BMGC_DS09449,BMG_DS035375,"testicular yolk sac tumor, solid pattern"
+BMGC_DS09450,BMG_DS035376,lymphoepithelioma-like acinar prostate adenocarcinoma
+BMGC_DS09451,BMG_DS035377,acinic cell breast carcinoma
+BMGC_DS09452,BMG_DS035378,adult vagina botryoid embryonal rhabdomyosarcoma
+BMGC_DS09453,BMG_DS035379,carcinoma of Cowper glands
+BMGC_DS09454,BMG_DS035380,Littre gland carcinoma
+BMGC_DS09455,BMG_DS035381,cellular neurofibroma
+BMGC_DS09456,BMG_DS035383,cervical adenoid basal carcinoma
+BMGC_DS09457,BMG_DS035384,cervical adenomyoma
+BMGC_DS09458,BMG_DS035385,endocervical type cervical adenomyoma
+BMGC_DS09459,BMG_DS035386,"cervical adenosquamous carcinoma, glassy cell variant"
+BMGC_DS09460,BMG_DS035387,cervical alveolar soft part sarcoma
+BMGC_DS09461,BMG_DS035388,cervical atypical polypoid adenomyoma
+BMGC_DS09462,BMG_DS035390,cervical large cell neuroendocrine carcinoma
+BMGC_DS09463,BMG_DS035391,cervical lymphoepithelioma-like carcinoma
+BMGC_DS09464,BMG_DS035392,Wolffian duct adenocarcinoma
+BMGC_DS09465,BMG_DS035393,cervical carcinosarcoma
+BMGC_DS09466,BMG_DS035394,intestinal variant cervical mucinous adenocarcinoma
+BMGC_DS09467,BMG_DS035395,"cervical mucinous adenocarcinoma, minimal deviation variant"
+BMGC_DS09468,BMG_DS035396,signet ring cell variant cervical mucinous adenocarcinoma
+BMGC_DS09469,BMG_DS035397,cervical adenosarcoma
+BMGC_DS09470,BMG_DS035399,cervical serous adenocarcinoma
+BMGC_DS09471,BMG_DS035400,cervical verrucous carcinoma
+BMGC_DS09472,BMG_DS035401,cervical Wilms tumor
+BMGC_DS09473,BMG_DS035402,classic congenital mesoblastic nephroma
+BMGC_DS09474,BMG_DS035403,cholangiolocellular carcinoma
+BMGC_DS09475,BMG_DS035404,cellular phase chronic idiopathic myelofibrosis
+BMGC_DS09476,BMG_DS035405,skin clear cell basal cell carcinoma
+BMGC_DS09477,BMG_DS035406,schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma
+BMGC_DS09478,BMG_DS035407,stroma-dominant and stroma-poor composite ganglioneuroblastoma
+BMGC_DS09479,BMG_DS035409,endometrial small cell carcinoma
+BMGC_DS09480,BMG_DS035410,endometrial transitional cell carcinoma
+BMGC_DS09481,BMG_DS035412,fallopian tube serous adenofibroma
+BMGC_DS09482,BMG_DS035414,fallopian tube cystadenofibroma
+BMGC_DS09483,BMG_DS035415,fallopian tube endometrioid tumor
+BMGC_DS09484,BMG_DS035416,fallopian tube germ cell tumor
+BMGC_DS09485,BMG_DS035418,fallopian tube leiomyosarcoma
+BMGC_DS09486,BMG_DS035419,fallopian tube carcinosarcoma
+BMGC_DS09487,BMG_DS035420,fallopian tube mucinous adenocarcinoma
+BMGC_DS09488,BMG_DS035422,fallopian tube adenosarcoma
+BMGC_DS09489,BMG_DS035424,fallopian tube serous adenocarcinoma
+BMGC_DS09490,BMG_DS035425,fallopian tube teratoma
+BMGC_DS09491,BMG_DS035426,fallopian tube transitional cell carcinoma
+BMGC_DS09492,BMG_DS035427,female urethral cancer
+BMGC_DS09493,BMG_DS035428,intermixed schwannian stroma-rich ganglioneuroblastoma
+BMGC_DS09494,BMG_DS035429,nodular ganglioneuroblastoma
+BMGC_DS09495,BMG_DS035430,gestational ovarian choriocarcinoma
+BMGC_DS09496,BMG_DS035431,micropapillary variant infiltrating bladder urothelial carcinoma
+BMGC_DS09497,BMG_DS035432,cervical keratinizing squamous cell carcinoma
+BMGC_DS09498,BMG_DS035433,late yaws
+BMGC_DS09499,BMG_DS035435,lipid-rich breast carcinoma
+BMGC_DS09500,BMG_DS035437,male urethral cancer
+BMGC_DS09501,BMG_DS035438,malignant breast myoepithelioma
+BMGC_DS09502,BMG_DS035439,cervical carcinosarcoma
+BMGC_DS09503,BMG_DS035441,ovarian endometrial cancer
+BMGC_DS09504,BMG_DS035442,mucinous ovarian cancer
+BMGC_DS09505,BMG_DS035443,malignant ovarian serous tumor
+BMGC_DS09506,BMG_DS035444,malignant ovarian surface epithelial-stromal neoplasm
+BMGC_DS09507,BMG_DS035445,non-gestational ovarian choriocarcinoma
+BMGC_DS09508,BMG_DS035446,non-invasive bladder papillary urothelial neoplasm
+BMGC_DS09509,BMG_DS035447,urinary tract non-invasive transitional cell neoplasm
+BMGC_DS09510,BMG_DS035448,cervical non-keratinizing squamous cell carcinoma
+BMGC_DS09511,BMG_DS035449,oncocytic breast carcinoma
+BMGC_DS09512,BMG_DS035450,ovarian biphasic or triphasic teratoma
+BMGC_DS09513,BMG_DS035451,ovarian clear cell adenocarcinoma
+BMGC_DS09514,BMG_DS035452,ovarian clear cell adenofibroma
+BMGC_DS09515,BMG_DS035453,ovarian clear cell cystadenofibroma
+BMGC_DS09516,BMG_DS035454,ovarian endometrioid adenocarcinofibroma
+BMGC_DS09517,BMG_DS035455,ovarian endometrioid cystadenoma
+BMGC_DS09518,BMG_DS035456,ovarian fetiform teratoma
+BMGC_DS09519,BMG_DS035457,ovarian gonadoblastoma
+BMGC_DS09520,BMG_DS035458,ovarian lymphoma
+BMGC_DS09521,BMG_DS035459,ovarian malignant mesothelioma
+BMGC_DS09522,BMG_DS035460,ovarian mucinous adenofibroma
+BMGC_DS09523,BMG_DS035461,ovarian mucinous cystadenofibroma
+BMGC_DS09524,BMG_DS035462,ovarian primitive germ cell tumor
+BMGC_DS09525,BMG_DS035463,ovarian serous adenofibroma
+BMGC_DS09526,BMG_DS035467,ovarian stromal hyperthecosis
+BMGC_DS09527,BMG_DS035468,ovarian Wilms tumor
+BMGC_DS09528,BMG_DS035469,"ovarian yolk sac tumor, glandular pattern"
+BMGC_DS09529,BMG_DS035470,"ovarian yolk sac tumor, hepatoid pattern"
+BMGC_DS09530,BMG_DS035471,"ovarian yolk sac tumor, polyvesicular vitelline pattern"
+BMGC_DS09531,BMG_DS035472,oxyphilic endometrial endometrioid adenocarcinoma
+BMGC_DS09532,BMG_DS035474,pancreatic mucinous-cystic neoplasm with an associated invasive carcinoma
+BMGC_DS09533,BMG_DS035475,pancreatic intraductal papillary-mucinous neoplasm with an associated invasive carcinoma
+BMGC_DS09534,BMG_DS035476,pancreatic mucinous-cystic neoplasm
+BMGC_DS09535,BMG_DS035477,pancreatic intraductal papillary-mucinous neoplasm with high grade dysplasia
+BMGC_DS09536,BMG_DS035478,pancreatic serous cystic neoplasm
+BMGC_DS09537,BMG_DS035479,chromophil adenoma of the kidney
+BMGC_DS09538,BMG_DS035480,bladder papillary urothelial carcinoma
+BMGC_DS09539,BMG_DS035481,penis basal cell carcinoma
+BMGC_DS09540,BMG_DS035482,penile urethral cancer
+BMGC_DS09541,BMG_DS035483,periductal breast myoepitheliosis
+BMGC_DS09542,BMG_DS035484,peripheral nerve schwannoma
+BMGC_DS09543,BMG_DS035485,pilomyxoid astrocytoma
+BMGC_DS09544,BMG_DS035487,pleomorphic adenoma
+BMGC_DS09545,BMG_DS035488,sarcomatoid basal cell carcinoma
+BMGC_DS09546,BMG_DS035489,sarcomatous intrahepatic cholangiocarcinoma
+BMGC_DS09547,BMG_DS035490,sebaceous breast carcinoma
+BMGC_DS09548,BMG_DS035491,seminal vesicle adenocarcinoma
+BMGC_DS09549,BMG_DS035492,seminal vesicle cystadenoma
+BMGC_DS09550,BMG_DS035493,signet ring basal cell carcinoma
+BMGC_DS09551,BMG_DS035494,signet ring cell intrahepatic cholangiocarcinoma
+BMGC_DS09552,BMG_DS035496,acantholytic variant squamous cell breast carcinoma
+BMGC_DS09553,BMG_DS035497,large cell keratinizing variant squamous cell breast carcinoma
+BMGC_DS09554,BMG_DS035498,spindle cell variant squamous cell breast carcinoma
+BMGC_DS09555,BMG_DS035500,type 1 papillary adenoma of the kidney
+BMGC_DS09556,BMG_DS035501,type 2 papillary adenoma of the kidney
+BMGC_DS09557,BMG_DS035503,ureter urothelial papilloma
+BMGC_DS09558,BMG_DS035504,urethral urothelial papilloma
+BMGC_DS09559,BMG_DS035505,urethral verrucous carcinoma
+BMGC_DS09560,BMG_DS035506,urethral villous adenoma
+BMGC_DS09561,BMG_DS035508,uterine corpus atypical polypoid adenomyoma
+BMGC_DS09562,BMG_DS035509,uterine corpus cellular leiomyoma
+BMGC_DS09563,BMG_DS035510,uterine corpus dissecting leiomyoma
+BMGC_DS09564,BMG_DS035511,uterine corpus endometrial stromal sarcoma
+BMGC_DS09565,BMG_DS035512,uterine corpus epithelioid leiomyoma
+BMGC_DS09566,BMG_DS035513,uterine corpus epithelioid leiomyosarcoma
+BMGC_DS09567,BMG_DS035514,uterine corpus apoplectic leiomyoma
+BMGC_DS09568,BMG_DS035517,uterine corpus lipoleiomyoma
+BMGC_DS09569,BMG_DS035519,endometrial mucinous adenocarcinoma
+BMGC_DS09570,BMG_DS035520,uterine corpus myxoid leiomyoma
+BMGC_DS09571,BMG_DS035521,uterine corpus myxoid leiomyosarcoma
+BMGC_DS09572,BMG_DS035522,uterine corpus perivascular epithelioid cell tumor
+BMGC_DS09573,BMG_DS035524,uterine ligament neoplasm
+BMGC_DS09574,BMG_DS035525,uterine ligament serous adenocarcinoma
+BMGC_DS09575,BMG_DS035527,vaginal adenoma
+BMGC_DS09576,BMG_DS035528,vaginal adenosarcoma
+BMGC_DS09577,BMG_DS035529,vaginal carcinosarcoma
+BMGC_DS09578,BMG_DS035530,vaginal glandular neoplasm
+BMGC_DS09579,BMG_DS035531,vaginal carcinosarcoma
+BMGC_DS09580,BMG_DS035533,vaginal squamous tumor
+BMGC_DS09581,BMG_DS035534,vaginal tubulovillous adenoma
+BMGC_DS09582,BMG_DS035535,vaginal villous adenoma
+BMGC_DS09583,BMG_DS035536,vestibular micropapillomatosis
+BMGC_DS09584,BMG_DS035537,vulvar alveolar soft part sarcoma
+BMGC_DS09585,BMG_DS035538,vulvar clear cell hidradenocarcinoma
+BMGC_DS09586,BMG_DS035539,vulvar eccrine porocarcinoma
+BMGC_DS09587,BMG_DS035540,vulvar glandular neoplasm
+BMGC_DS09588,BMG_DS035542,vulvar inverted follicular keratosis
+BMGC_DS09589,BMG_DS035545,vulvar non-keratinizing squamous cell carcinoma
+BMGC_DS09590,BMG_DS035546,vulvar proximal-type epithelioid sarcoma
+BMGC_DS09591,BMG_DS035547,vulvar sebaceous carcinoma
+BMGC_DS09592,BMG_DS035548,vulvar squamous neoplasm
+BMGC_DS09593,BMG_DS035551,Wolffian adnexal tumor
+BMGC_DS09594,BMG_DS035552,Intermittent cerebral ischemia
+BMGC_DS09595,BMG_DS035555,Bonnevie-Ullrich Syndrome
+BMGC_DS09596,BMG_DS035557,CRST syndrome
+BMGC_DS09597,BMG_DS035558,Adrenomyeloneuropathy
+BMGC_DS09598,BMG_DS035560,Dental Pulp Stone
+BMGC_DS09599,BMG_DS035563,Chronic Airflow Obstruction
+BMGC_DS09600,BMG_DS035564,Ametropia
+BMGC_DS09601,BMG_DS035565,brain edema
+BMGC_DS09602,BMG_DS035566,Alpha-Aminoadipic Semialdehyde Deficiency Disease
+BMGC_DS09603,BMG_DS035568,"Vertigo, Aural"
+BMGC_DS09604,BMG_DS035569,Pyridoxine Deficiency
+BMGC_DS09605,BMG_DS035570,"Transient Ischemic Attack, Anterior Circulation"
+BMGC_DS09606,BMG_DS035571,Sjogren's Syndrome
+BMGC_DS09607,BMG_DS035572,"Familial Amyloid Polyneuropathy, Appalachian Type"
+BMGC_DS09608,BMG_DS035573,"Hereditary Cerebral Amyloid Angiopathy, Icelandic Type"
+BMGC_DS09609,BMG_DS035574,breast ductal adenocarcinoma
+BMGC_DS09610,BMG_DS035575,Nerve Root Disorder
+BMGC_DS09611,BMG_DS035576,Hepatic Form of Wilson Disease
+BMGC_DS09612,BMG_DS035577,Algodystrophic Syndrome
+BMGC_DS09613,BMG_DS035579,Phototoxicity
+BMGC_DS09614,BMG_DS035580,Salaam Seizures
+BMGC_DS09615,BMG_DS035581,Vincent Angina
+BMGC_DS09616,BMG_DS035582,Cystic Breast Disease
+BMGC_DS09617,BMG_DS035583,Morphea
+BMGC_DS09618,BMG_DS035586,Ogilvie Syndrome
+BMGC_DS09619,BMG_DS035587,Fibrocystic Disease of Pancreas
+BMGC_DS09620,BMG_DS035590,Rhizomelic pseudopolyarthritis
+BMGC_DS09621,BMG_DS035591,Eosinophilic Pneumonia
+BMGC_DS09622,BMG_DS035592,Renal rickets
+BMGC_DS09623,BMG_DS035593,Thrombosis of retinal vein
+BMGC_DS09624,BMG_DS035594,adenocarcinoma of skene gland origin
+BMGC_DS09625,BMG_DS035616,atherosclerosis susceptibility
+BMGC_DS09626,BMG_DS035618,Currarino triad
+BMGC_DS09627,BMG_DS035650,Disorder of immune function
+BMGC_DS09628,BMG_DS035662,Infectious Endophthalmitis
+BMGC_DS09629,BMG_DS035708,Primary congenital glaucoma
+BMGC_DS09630,BMG_DS035720,Chronic coronary insufficiency
+BMGC_DS09631,BMG_DS035723,Pseudo-Zellweger syndrome
+BMGC_DS09632,BMG_DS035730,Disorder of skeletal muscle
+BMGC_DS09633,BMG_DS035732,Bleeding of subgingival space
+BMGC_DS09634,BMG_DS036050,neurocirculatory asthenia
+BMGC_DS09635,BMG_DS036052,neurodevelopmental disorder
+BMGC_DS09636,BMG_DS036053,pneumocystosis
+BMGC_DS09637,BMG_DS036054,Polyglandular Type III Autoimmune Syndrome
+BMGC_DS09638,BMG_DS036058,Dysbacteriosis
+BMGC_DS09639,BMG_DS036069,Central areolar choroidal sclerosis
+BMGC_DS09640,BMG_DS036080,Deficiency of acetyl-CoA acetyltransferase
+BMGC_DS09641,BMG_DS036144,"Chronic obstructive lung disease, NEC"
+BMGC_DS09642,BMG_DS036273,Pyloric obstruction
+BMGC_DS09643,BMG_DS036363,Infective endocarditis
+BMGC_DS09644,BMG_DS036424,Pancytopenia-dysmelia syndrome
+BMGC_DS09645,BMG_DS036496,Chronic Kidney Diseases
+BMGC_DS09646,BMG_DS036497,Overweight and obesity
+BMGC_DS09647,BMG_DS036499,Anemia in chronic kidney disease
+BMGC_DS09648,BMG_DS036533,Fleck corneal dystrophy
+BMGC_DS09649,BMG_DS036559,Ocular histoplasmosis syndrome
+BMGC_DS09650,BMG_DS036560,"Leprosy, Multibacillary"
+BMGC_DS09651,BMG_DS036566,Acute cerebellar syndrome
+BMGC_DS09652,BMG_DS036574,Twin reversal arterial perfusion syndrome
+BMGC_DS09653,BMG_DS036581,Thiel-Behnke corneal dystrophy
+BMGC_DS09654,BMG_DS036584,"Leprosy, Paucibacillary"
+BMGC_DS09655,BMG_DS036592,Dapsone resistant leprosy
+BMGC_DS09656,BMG_DS036624,DNA Repair-Deficiency Disorders
+BMGC_DS09657,BMG_DS036625,Chromosome Instability Syndromes
+BMGC_DS09658,BMG_DS036626,"Nephrogenic Diabetes Insipidus, Type I"
+BMGC_DS09659,BMG_DS036627,"Nephrogenic Diabetes Insipidus, Type II"
+BMGC_DS09660,BMG_DS036628,Myopathic Ophthalmopathy
+BMGC_DS09661,BMG_DS036629,Andersen Syndrome
+BMGC_DS09662,BMG_DS036630,Genital Infantilism
+BMGC_DS09663,BMG_DS036631,Kallmann Syndrome 1
+BMGC_DS09664,BMG_DS036632,Kallmann Syndrome 2
+BMGC_DS09665,BMG_DS036635,"Headache Disorders, Primary"
+BMGC_DS09666,BMG_DS036639,Cholera Infantum
+BMGC_DS09667,BMG_DS036640,Renal Insufficiency
+BMGC_DS09668,BMG_DS036641,Acute Kidney Insufficiency
+BMGC_DS09669,BMG_DS036642,"Direct Hyperbilirubinemia, Neonatal"
+BMGC_DS09670,BMG_DS036643,"Indirect Hyperbilirubinemia, Neonatal"
+BMGC_DS09671,BMG_DS036645,posterior cranial fossa meningioma
+BMGC_DS09672,BMG_DS036646,Icterus Gravis Neonatorum
+BMGC_DS09673,BMG_DS036647,Preterm Premature Rupture of Fetal Membranes
+BMGC_DS09674,BMG_DS036648,Unilateral Multicystic Dysplastic Kidney
+BMGC_DS09675,BMG_DS036649,Alport Syndrome
+BMGC_DS09676,BMG_DS036650,"Alport Syndrome, X-Linked"
+BMGC_DS09677,BMG_DS036651,"Alport Syndrome, Autosomal Dominant"
+BMGC_DS09678,BMG_DS036652,"Alport Syndrome, Autosomal Recessive"
+BMGC_DS09679,BMG_DS036653,Usher syndrome type 1
+BMGC_DS09680,BMG_DS036654,"Usher Syndrome, Type III"
+BMGC_DS09681,BMG_DS036655,"Usher Syndrome, Type II"
+BMGC_DS09682,BMG_DS036656,Tendinopathy
+BMGC_DS09683,BMG_DS036657,Tendinosis
+BMGC_DS09684,BMG_DS036658,Oral Mucositis
+BMGC_DS09685,BMG_DS036762,Renotubular acidemia
+BMGC_DS09686,BMG_DS036782,(Vaginitis &/or vulvovaginitis (& non specified)) or (bacterial vaginosis) or (vulvitis non specified)
+BMGC_DS09687,BMG_DS036785,"Myxedema, Congenital"
+BMGC_DS09688,BMG_DS036825,islet cell adenomatosis
+BMGC_DS09689,BMG_DS036844,Chronic uremia
+BMGC_DS09690,BMG_DS036923,Megacystis microcolon intestinal hypoperistalsis syndrome
+BMGC_DS09691,BMG_DS036927,Mycobacterium abscessus Infection
+BMGC_DS09692,BMG_DS036929,Congenital absence of kidneys syndrome
+BMGC_DS09693,BMG_DS036931,Latent Tuberculosis
+BMGC_DS09694,BMG_DS036943,Nephrogenic Fibrosing Dermopathy
+BMGC_DS09695,BMG_DS036944,renal hypodysplasia/aplasia 1
+BMGC_DS09696,BMG_DS036945,Decompensated cirrhosis of liver
+BMGC_DS09697,BMG_DS036946,Gout flare
+BMGC_DS09698,BMG_DS036953,Partial atrioventricular block
+BMGC_DS09699,BMG_DS036955,Adrenal hyperplasia
+BMGC_DS09700,BMG_DS036956,Intermediate Maple Syrup Urine Disease
+BMGC_DS09701,BMG_DS036957,Meretoja syndrome
+BMGC_DS09702,BMG_DS036959,"Corneal Dystrophy, Central Type"
+BMGC_DS09703,BMG_DS036963,Cirrhosis
+BMGC_DS09704,BMG_DS036964,Okihiro Syndrome
+BMGC_DS09705,BMG_DS036995,"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY"
+BMGC_DS09706,BMG_DS036996,Complicated appendicitis
+BMGC_DS09707,BMG_DS037005,"Macular dystrophy, corneal type 1"
+BMGC_DS09708,BMG_DS037026,Groenouw corneal dystrophy type I (disorder)
+BMGC_DS09709,BMG_DS037035,Ectopia Lentis with Ectopia of Pupil
+BMGC_DS09710,BMG_DS037038,early-onset schizophrenia
+BMGC_DS09711,BMG_DS037057,Intraoperative floppy iris syndrome
+BMGC_DS09712,BMG_DS037063,Lattice corneal dystrophy Type I
+BMGC_DS09713,BMG_DS037073,Macular corneal dystrophy Type II (disorder)
+BMGC_DS09714,BMG_DS037077,Cystic Kidney Diseases
+BMGC_DS09715,BMG_DS037084,"Arthritis, Bacterial"
+BMGC_DS09716,BMG_DS037088,Bacterial tonsillitis
+BMGC_DS09717,BMG_DS037092,Spontaneous hematomas
+BMGC_DS09718,BMG_DS037093,BK virus nephropathy
+BMGC_DS09719,BMG_DS037096,Bacterial otitis media
+BMGC_DS09720,BMG_DS037097,Bacterial otitis externa
+BMGC_DS09721,BMG_DS037099,"Pneumonia, Ventilator-Associated"
+BMGC_DS09722,BMG_DS037104,neoplastic meningitis
+BMGC_DS09723,BMG_DS037106,benign prostatic hyperplasia
+BMGC_DS09724,BMG_DS037109,Pyomyositis
+BMGC_DS09725,BMG_DS037110,"Hypobetalipoproteinemia, Familial, Apolipoprotein B"
+BMGC_DS09726,BMG_DS037111,Leukokeratosis
+BMGC_DS09727,BMG_DS037112,"Nephrotic Syndrome, Minimal Change"
+BMGC_DS09728,BMG_DS037116,Dental Diseases
+BMGC_DS09729,BMG_DS037117,Hypophosphatemic Rickets
+BMGC_DS09730,BMG_DS037119,Bright Disease
+BMGC_DS09731,BMG_DS037120,Heymann Nephritis
+BMGC_DS09732,BMG_DS037121,Distal Renal Tubular Acidosis
+BMGC_DS09733,BMG_DS037123,Hyperlipoproteinemia Type IIb
+BMGC_DS09734,BMG_DS037125,Milroy Disease
+BMGC_DS09735,BMG_DS037126,Hereditary lymphedema type II
+BMGC_DS09736,BMG_DS037128,"Hypoalphalipoproteinemia, Familial"
+BMGC_DS09737,BMG_DS037129,Urinary Schistosomiasis
+BMGC_DS09738,BMG_DS037130,Peripheral Arterial Diseases
+BMGC_DS09739,BMG_DS037133,Hyperparathyroidism-Jaw Tumor Syndrome
+BMGC_DS09740,BMG_DS037141,"Pachyonychia Congenita, Jadassohn Lewandowsky Type"
+BMGC_DS09741,BMG_DS037142,adult myxoid chondrosarcoma
+BMGC_DS09742,BMG_DS037143,aldosterone-producing adrenal cortex adenoma
+BMGC_DS09743,BMG_DS037147,nut midline carcinoma
+BMGC_DS09744,BMG_DS037150,classic medulloblastoma
+BMGC_DS09745,BMG_DS037164,hereditary diffuse gastric adenocarcinoma
+BMGC_DS09746,BMG_DS037165,hereditary leiomyomatosis and renal cell cancer
+BMGC_DS09747,BMG_DS037166,hereditary pheochromocytoma-paraganglioma
+BMGC_DS09748,BMG_DS037168,histiocytoid cardiomyopathy
+BMGC_DS09749,BMG_DS037177,lung sarcomatoid carcinoma
+BMGC_DS09750,BMG_DS037185,Osteofibrous Dysplasia
+BMGC_DS09751,BMG_DS037198,sinonasal undifferentiated carcinoma
+BMGC_DS09752,BMG_DS037203,Familial spinal arachnoiditis
+BMGC_DS09753,BMG_DS037208,melanoma in congenital melanocytic nevus
+BMGC_DS09754,BMG_DS037220,Acquired torsion dystonia
+BMGC_DS09755,BMG_DS037224,Idiopathic transverse myelitis
+BMGC_DS09756,BMG_DS037249,Severe Sepsis
+BMGC_DS09757,BMG_DS037262,Episodic ataxia type 1
+BMGC_DS09758,BMG_DS037279,Meningitis caused by Klebsiella aerogenes
+BMGC_DS09759,BMG_DS037284,Disorder due to type 2 diabetes mellitus
+BMGC_DS09760,BMG_DS037305,Gastrointestinal infection caused by Klebsiella aerogenes
+BMGC_DS09761,BMG_DS037309,Herpes zoster with AIDS (acquired immunodeficiency syndrome)
+BMGC_DS09762,BMG_DS037318,Episodic Ataxia
+BMGC_DS09763,BMG_DS037342,"Episodic Ataxia, Type 2"
+BMGC_DS09764,BMG_DS037352,Toxoplasmosis associated with acquired immunodeficiency syndrome
+BMGC_DS09765,BMG_DS037353,Adult growth hormone deficiency
+BMGC_DS09766,BMG_DS037381,hydrocele
+BMGC_DS09767,BMG_DS037382,Hypoprebetalipoproteinemia
+BMGC_DS09768,BMG_DS037383,Glomerular Necrosis
+BMGC_DS09769,BMG_DS037385,familial apolipoprotein C-II deficiency
+BMGC_DS09770,BMG_DS037386,"Meningitis, Pneumococcal, Recurrent"
+BMGC_DS09771,BMG_DS037387,Acute Bacterial Prostatitis
+BMGC_DS09772,BMG_DS037388,Asymptomatic Inflammatory Prostatitis
+BMGC_DS09773,BMG_DS037389,Chronic Bacterial Prostatitis
+BMGC_DS09774,BMG_DS037390,"Refsum Disease, Phytanoyl-CoA Hydroxylase Deficiency"
+BMGC_DS09775,BMG_DS037392,Endometrial Diseases
+BMGC_DS09776,BMG_DS037393,"Membranoproliferative Glomerulonephritis, Type III"
+BMGC_DS09777,BMG_DS037394,sudden cardiac arrest
+BMGC_DS09778,BMG_DS037395,Painful Bladder Syndrome
+BMGC_DS09779,BMG_DS037397,"Familial Partial Lipodystrophy, Type 1"
+BMGC_DS09780,BMG_DS037398,"Familial Partial Lipodystrophy, Type 2"
+BMGC_DS09781,BMG_DS037399,"Familial Partial Lipodystrophy, Type 3"
+BMGC_DS09782,BMG_DS037400,Congenital Generalized Lipodystrophy Type 1
+BMGC_DS09783,BMG_DS037401,congenital generalized lipodystrophy type 2
+BMGC_DS09784,BMG_DS037402,"Sulfatidosis, Juvenile, Austin Type"
+BMGC_DS09785,BMG_DS037403,Female Urogenital Diseases
+BMGC_DS09786,BMG_DS037404,Male Urogenital Diseases
+BMGC_DS09787,BMG_DS037405,"Hyper-IgM Immunodeficiency Syndrome, Type 2"
+BMGC_DS09788,BMG_DS037406,"Hyper-IgM Immunodeficiency Syndrome, Type 3"
+BMGC_DS09789,BMG_DS037407,"Hyper-IgM Immunodeficiency Syndrome, Type 5"
+BMGC_DS09790,BMG_DS037408,"Ectodermal Dysplasia 3, Anhidrotic"
+BMGC_DS09791,BMG_DS037409,Channelopathies
+BMGC_DS09792,BMG_DS037411,"Leukokeratosis, Hereditary Mucosal"
+BMGC_DS09793,BMG_DS037412,"Keratoderma, Palmoplantar, Epidermolytic"
+BMGC_DS09794,BMG_DS037413,"Pachyonychia Congenita, Type 2"
+BMGC_DS09795,BMG_DS037415,Paraneoplastic Opsoclonus-Myoclonus Ataxia
+BMGC_DS09796,BMG_DS037417,Brugada syndrome
+BMGC_DS09797,BMG_DS037418,Chronic Prostatitis with Chronic Pelvic Pain Syndrome
+BMGC_DS09798,BMG_DS037420,Migraine with Typical Aura
+BMGC_DS09799,BMG_DS037423,Bland White Garland Syndrome
+BMGC_DS09800,BMG_DS037434,Latent Autoimmune Diabetes in Adults
+BMGC_DS09801,BMG_DS037436,Prostatic Hypertrophy
+BMGC_DS09802,BMG_DS037437,Angel-shaped phalango-epiphyseal dysplasia
+BMGC_DS09803,BMG_DS037438,Takotsubo Cardiomyopathy
+BMGC_DS09804,BMG_DS037442,Congenital ectodermal dysplasia of face
+BMGC_DS09805,BMG_DS037446,Aspiration pneumonitis
+BMGC_DS09806,BMG_DS037447,RAPP-HODGKIN SYNDROME
+BMGC_DS09807,BMG_DS037448,Idiopathic Pulmonary Fibrosis
+BMGC_DS09808,BMG_DS037449,Congenital muscular hypertrophy-cerebral syndrome
+BMGC_DS09809,BMG_DS037452,Familial benign hypercalcemia
+BMGC_DS09810,BMG_DS037454,Variola major
+BMGC_DS09811,BMG_DS037455,"DEAFNESS, AUTOSOMAL RECESSIVE 70"
+BMGC_DS09812,BMG_DS037478,Decompensated chronic heart failure
+BMGC_DS09813,BMG_DS037482,Extensively Drug-Resistant Tuberculosis
+BMGC_DS09814,BMG_DS037488,Poor metabolizer due to cytochrome p450 CYP2C9 variant
+BMGC_DS09815,BMG_DS037492,Slow acetylator due to N-acetyltransferase enzyme variant
+BMGC_DS09816,BMG_DS037499,Poor metabolizer due to cytochrome p450 CYP2C19 variant
+BMGC_DS09817,BMG_DS037525,Ultrarapid metabolizer due to cytochrome p450 CYP2D6 variant
+BMGC_DS09818,BMG_DS037547,Prepapillary vascular loops
+BMGC_DS09819,BMG_DS037558,"Macular dystrophy, concentric annular"
+BMGC_DS09820,BMG_DS037573,Poor metabolizer due to cytochrome p450 CYP2D6 variant
+BMGC_DS09821,BMG_DS037582,Carnitine palmitoyl transferase 1A deficiency
+BMGC_DS09822,BMG_DS037584,Wilms tumor 5
+BMGC_DS09823,BMG_DS037587,"HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY"
+BMGC_DS09824,BMG_DS037588,"Ectopia Lentis, Spontaneous Filtering Blebs, and Craniofacial Dysmorphism"
+BMGC_DS09825,BMG_DS037589,DOYNE HONEYCOMB RETINAL DYSTROPHY
+BMGC_DS09826,BMG_DS037590,"Cataract, Congenital, Cerulean Type, 2"
+BMGC_DS09827,BMG_DS037591,"Deafness, Autosomal Dominant 12"
+BMGC_DS09828,BMG_DS037592,Peroxisome biogenesis disorders
+BMGC_DS09829,BMG_DS037594,Athabaskan brainstem dysgenesis
+BMGC_DS09830,BMG_DS037595,Bosley-Salih-Alorainy Syndrome
+BMGC_DS09831,BMG_DS037596,Rieger syndrome 2
+BMGC_DS09832,BMG_DS037600,"Agammaglobulinemia, non-Bruton type"
+BMGC_DS09833,BMG_DS037601,"Cardiomyopathy, Dilated, 1D"
+BMGC_DS09834,BMG_DS037602,"Cardiomyopathy, Dilated, 1C"
+BMGC_DS09835,BMG_DS037603,Ribbing disease
+BMGC_DS09836,BMG_DS037604,"Charcot-Marie-Tooth disease, Type 2D"
+BMGC_DS09837,BMG_DS037605,"FACIAL PARESIS, HEREDITARY CONGENITAL, 1"
+BMGC_DS09838,BMG_DS037607,"Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive"
+BMGC_DS09839,BMG_DS037608,"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D"
+BMGC_DS09840,BMG_DS037612,"Deafness, Progressive, With Stapes Fixation"
+BMGC_DS09841,BMG_DS037613,Rhizomelic dysplasia Patterson Lowry type
+BMGC_DS09842,BMG_DS037614,Jung Wolff Back Stahl syndrome
+BMGC_DS09843,BMG_DS037616,"MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED"
+BMGC_DS09844,BMG_DS037617,Retinitis Pigmentosa 18
+BMGC_DS09845,BMG_DS037618,"Deafness, Autosomal Dominant 7"
+BMGC_DS09846,BMG_DS037619,"Diabetes Mellitus, Transient Neonatal, 1"
+BMGC_DS09847,BMG_DS037621,"Platelet Disorder, Familial, with Associated Myeloid Malignancy"
+BMGC_DS09848,BMG_DS037622,Van Maldergem Wetzburger Verloes syndrome
+BMGC_DS09849,BMG_DS037623,Cervical ribs sprengel anomaly anal atresia urethral obstruction
+BMGC_DS09850,BMG_DS037624,"DIABETES MELLITUS, INSULIN-DEPENDENT, 12"
+BMGC_DS09851,BMG_DS037625,"Deafness, Autosomal Recessive 12"
+BMGC_DS09852,BMG_DS037626,"Charcot-Marie-Tooth disease, Type 4B1"
+BMGC_DS09853,BMG_DS037627,Hunter-McAlpine craniosynostosis syndrome
+BMGC_DS09854,BMG_DS037628,Crisponi syndrome
+BMGC_DS09855,BMG_DS037631,Aprosencephaly and Cerebellar Dysgenesis
+BMGC_DS09856,BMG_DS037633,early-onset non-syndromic cataract
+BMGC_DS09857,BMG_DS037634,Genoa syndrome
+BMGC_DS09858,BMG_DS037635,"Deafness, Autosomal Dominant 9"
+BMGC_DS09859,BMG_DS037636,Wilms tumor 4
+BMGC_DS09860,BMG_DS037637,Digeorge Syndrome-Velocardiofacial Syndrome Complex 2
+BMGC_DS09861,BMG_DS037638,"Amelia, Autosomal Recessive"
+BMGC_DS09862,BMG_DS037640,Yim Ebbin syndrome
+BMGC_DS09863,BMG_DS037641,Short limb dwarfism Al Gazali type
+BMGC_DS09864,BMG_DS037642,"Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs"
+BMGC_DS09865,BMG_DS037643,"Mental Retardation, Microcephaly, Epilepsy, And Coarse Face"
+BMGC_DS09866,BMG_DS037646,"MICROPHTHALMIA, SYNDROMIC 8"
+BMGC_DS09867,BMG_DS037649,Martinez-Frias Syndrome
+BMGC_DS09868,BMG_DS037650,"Ectodermal Dysplasia with Natal Teeth, Turnpenny Type"
+BMGC_DS09869,BMG_DS037651,"Spinal Dysplasia, Anhalt Type"
+BMGC_DS09870,BMG_DS037652,"Atrophia Maculosa Varioliformis Cutis, Familial"
+BMGC_DS09871,BMG_DS037653,CAPOS syndrome
+BMGC_DS09872,BMG_DS037655,Porencephaly cerebellar hypoplasia malformations
+BMGC_DS09873,BMG_DS037656,Odontomicronychial dysplasia
+BMGC_DS09874,BMG_DS037658,"Deafness, Autosomal Dominant 11"
+BMGC_DS09875,BMG_DS037659,"Deafness, Autosomal Dominant 10"
+BMGC_DS09876,BMG_DS037662,Limb-girdle muscular dystrophy type 2F
+BMGC_DS09877,BMG_DS037664,"Diabetes Mellitus, Noninsulin-Dependent, 1"
+BMGC_DS09878,BMG_DS037665,autosomal recessive congenital ichthyosis 4A
+BMGC_DS09879,BMG_DS037666,Rippling Muscle Disease 2
+BMGC_DS09880,BMG_DS037667,"CEREBELLAR ATAXIA, CAYMAN TYPE"
+BMGC_DS09881,BMG_DS037668,"DERMATITIS HERPETIFORMIS, FAMILIAL"
+BMGC_DS09882,BMG_DS037669,"POLYPOSIS SYNDROME, HEREDITARY MIXED, 1"
+BMGC_DS09883,BMG_DS037670,Chromosome 11p11.2 Deletion Syndrome
+BMGC_DS09884,BMG_DS037671,"Neuronal Intestinal Dysplasia, Type B"
+BMGC_DS09885,BMG_DS037675,Verloes Bourguignon syndrome
+BMGC_DS09886,BMG_DS037676,Naxos disease
+BMGC_DS09887,BMG_DS037678,Anterior polar cataract 2
+BMGC_DS09888,BMG_DS037680,"Hypocalcemia, Autosomal Dominant, with Bartter Syndrome"
+BMGC_DS09889,BMG_DS037681,"HYPERPARATHYROIDISM, NEONATAL SEVERE"
+BMGC_DS09890,BMG_DS037682,Hypoparathyroidism familial isolated
+BMGC_DS09891,BMG_DS037683,Anophthalmia with pulmonary hypoplasia
+BMGC_DS09892,BMG_DS037684,"myocardial infarction, susceptibility to"
+BMGC_DS09893,BMG_DS037686,"Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects Of Skull"
+BMGC_DS09894,BMG_DS037687,"Spastic paraplegia 9, autosomal dominant"
+BMGC_DS09895,BMG_DS037690,"CARDIOMYOPATHY, DILATED, 1E"
+BMGC_DS09896,BMG_DS037691,brachydactyly type A2
+BMGC_DS09897,BMG_DS037692,MULTIPLE SYNOSTOSES SYNDROME 2
+BMGC_DS09898,BMG_DS037693,Fallot complex with severe mental and growth retardation
+BMGC_DS09899,BMG_DS037694,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id"
+BMGC_DS09900,BMG_DS037697,"Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation"
+BMGC_DS09901,BMG_DS037698,"Laterality Defects, Autosomal Dominant"
+BMGC_DS09902,BMG_DS037699,"Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction"
+BMGC_DS09903,BMG_DS037700,"DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8"
+BMGC_DS09904,BMG_DS037701,"Deafness, Autosomal Recessive 9"
+BMGC_DS09905,BMG_DS037703,"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1"
+BMGC_DS09906,BMG_DS037704,"USHER SYNDROME, TYPE ID"
+BMGC_DS09907,BMG_DS037705,"CHOREOATHETOSIS/SPASTICITY, EPISODIC"
+BMGC_DS09908,BMG_DS037706,Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin
+BMGC_DS09909,BMG_DS037709,"Hemiplegic migraine, familial type 1"
+BMGC_DS09910,BMG_DS037710,"MIGRAINE, SPORADIC HEMIPLEGIC"
+BMGC_DS09911,BMG_DS037711,Timothy syndrome
+BMGC_DS09912,BMG_DS037712,"Portal Vein, Cavernous Transformation Of"
+BMGC_DS09913,BMG_DS037713,Brody myopathy
+BMGC_DS09914,BMG_DS037714,"Epidermolysis Bullosa Simplex, Autosomal Recessive"
+BMGC_DS09915,BMG_DS037715,"Deafness, Autosomal Dominant 5"
+BMGC_DS09916,BMG_DS037716,JUVENILE POLYPOSIS OF STOMACH
+BMGC_DS09917,BMG_DS037717,Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia
+BMGC_DS09918,BMG_DS037719,Infundibulopelvic dysgenesis
+BMGC_DS09919,BMG_DS037720,"Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies"
+BMGC_DS09920,BMG_DS037721,Cone-Rod Dystrophy 5
+BMGC_DS09921,BMG_DS037722,"GLAUCOMA 3, PRIMARY INFANTILE, B"
+BMGC_DS09922,BMG_DS037723,"Deafness, Autosomal Recessive 7"
+BMGC_DS09923,BMG_DS037724,"DEAFNESS, AUTOSOMAL RECESSIVE 6"
+BMGC_DS09924,BMG_DS037725,"EPIPHYSEAL DYSPLASIA, MULTIPLE, 3"
+BMGC_DS09925,BMG_DS037726,"DEAFNESS, AUTOSOMAL DOMINANT 6"
+BMGC_DS09926,BMG_DS037728,"PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC"
+BMGC_DS09927,BMG_DS037729,Proprotein Convertase 1 3 Deficiency
+BMGC_DS09928,BMG_DS037730,permanent neonatal diabetes mellitus
+BMGC_DS09929,BMG_DS037732,pulverulent cataract
+BMGC_DS09930,BMG_DS037733,Marden Walker like syndrome
+BMGC_DS09931,BMG_DS037734,Long Qt Syndrome 4
+BMGC_DS09932,BMG_DS037738,"Hyperferritinemia, hereditary, with congenital cataracts"
+BMGC_DS09933,BMG_DS037740,"Charcot-Marie-Tooth disease, Type 2B"
+BMGC_DS09934,BMG_DS037741,"Cataract, Congenital Zonular, with Sutural Opacities"
+BMGC_DS09935,BMG_DS037742,"Cardiomyopathy, Familial Hypertrophic, 6"
+BMGC_DS09936,BMG_DS037743,Retinitis Pigmentosa 17
+BMGC_DS09937,BMG_DS037745,SCHIZOPHRENIA 4
+BMGC_DS09938,BMG_DS037746,"Enuresis, Nocturnal, 2"
+BMGC_DS09939,BMG_DS037747,"Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative"
+BMGC_DS09940,BMG_DS037749,"FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED"
+BMGC_DS09941,BMG_DS037750,"neuronopathy, distal hereditary motor, type 5"
+BMGC_DS09942,BMG_DS037751,"Deafness, Autosomal Recessive 5"
+BMGC_DS09943,BMG_DS037752,"CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL"
+BMGC_DS09944,BMG_DS037753,Anophthalmia plus syndrome
+BMGC_DS09945,BMG_DS037754,Synostotic Posterior Plagiocephaly
+BMGC_DS09946,BMG_DS037756,OROFACIAL CLEFT 3
+BMGC_DS09947,BMG_DS037757,"HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III"
+BMGC_DS09948,BMG_DS037758,"Inclusion Body Myopathy, Autosomal Recessive"
+BMGC_DS09949,BMG_DS037760,"Maturity-Onset Diabetes of the Young, Type 4"
+BMGC_DS09950,BMG_DS037761,D-2-hydroxyglutaric aciduria
+BMGC_DS09951,BMG_DS037762,Proximal Myopathy with Focal Depletion of Mitochondria
+BMGC_DS09952,BMG_DS037763,Satoyoshi syndrome
+BMGC_DS09953,BMG_DS037765,"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5"
+BMGC_DS09954,BMG_DS037766,Microtia-Anotia
+BMGC_DS09955,BMG_DS037767,"Varicella, Severe Recurrent"
+BMGC_DS09956,BMG_DS037768,Chondrocalcinosis 1
+BMGC_DS09957,BMG_DS037769,"Deafness, Autosomal Dominant 4"
+BMGC_DS09958,BMG_DS037770,"carnitine palmitoyl transferase II deficiency, myopathic form"
+BMGC_DS09959,BMG_DS037771,"CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE"
+BMGC_DS09960,BMG_DS037772,"CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL"
+BMGC_DS09961,BMG_DS037773,OROFACIAL CLEFT 7
+BMGC_DS09962,BMG_DS037775,UV-Sensitive Syndrome
+BMGC_DS09963,BMG_DS037777,Cone-Rod Dystrophy 1
+BMGC_DS09964,BMG_DS037779,"Craniosynostosis, Adelaide Type"
+BMGC_DS09965,BMG_DS037780,Spondyloepiphyseal Dysplasia with Atlantoaxial Instability
+BMGC_DS09966,BMG_DS037781,"Hydrocephalus, endocardial fibroelastosis, and cataracts"
+BMGC_DS09967,BMG_DS037782,PAROXYSMAL EXTREME PAIN DISORDER
+BMGC_DS09968,BMG_DS037783,inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+BMGC_DS09969,BMG_DS037784,Pacman dysplasia
+BMGC_DS09970,BMG_DS037785,"nephrolithiasis, calcium oxalate"
+BMGC_DS09971,BMG_DS037786,"Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension"
+BMGC_DS09972,BMG_DS037787,"Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis"
+BMGC_DS09973,BMG_DS037789,Otofaciocervical Syndrome
+BMGC_DS09974,BMG_DS037790,"otitis media, susceptibility to"
+BMGC_DS09975,BMG_DS037791,Otodental Dysplasia
+BMGC_DS09976,BMG_DS037792,Osteosclerosis with Ichthyosis and Fractures
+BMGC_DS09977,BMG_DS037793,Osteopoikilosis and dacryocystitis
+BMGC_DS09978,BMG_DS037794,"Osteopoikilosis, Isolated"
+BMGC_DS09979,BMG_DS037797,Osteomas Of Mandible
+BMGC_DS09980,BMG_DS037798,"Osteogenesis imperfecta, Levin type"
+BMGC_DS09981,BMG_DS037800,"Ossicular Malformations, familial"
+BMGC_DS09982,BMG_DS037801,Ossified Ear Cartilages
+BMGC_DS09983,BMG_DS037802,Oslam syndrome
+BMGC_DS09984,BMG_DS037803,"Orbital Margin, Hypoplasia of"
+BMGC_DS09985,BMG_DS037804,Orofaciodigital Syndrome X
+BMGC_DS09986,BMG_DS037805,"Optic Nerve Hypoplasia, Bilateral"
+BMGC_DS09987,BMG_DS037806,"Optic Nerve Aplasia, Bilateral"
+BMGC_DS09988,BMG_DS037808,"OPTIC ATROPHY AND CATARACT, AUTOSOMAL DOMINANT"
+BMGC_DS09989,BMG_DS037810,"Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant"
+BMGC_DS09990,BMG_DS037811,"Ophthalmoplegia, Progressive, with Scrotal Tongue and Mental Deficiency"
+BMGC_DS09991,BMG_DS037812,"Ophthalmoplegia, Familial Total, with Iris Transillumination"
+BMGC_DS09992,BMG_DS037813,"Ophthalmoplegia, Familial Static"
+BMGC_DS09993,BMG_DS037814,Ophthalmomandibulomelic Dysplasia
+BMGC_DS09994,BMG_DS037815,"Onycholysis, Partial, with Scleronychia"
+BMGC_DS09995,BMG_DS037816,familial medullary thyroid carcinoma
+BMGC_DS09996,BMG_DS037820,Oculopharyngodistal Myopathy
+BMGC_DS09997,BMG_DS037821,Schilbach-Rott syndrome
+BMGC_DS09998,BMG_DS037823,Hereditary vertical nystagmus
+BMGC_DS09999,BMG_DS037824,"Nystagmus 2, congenital, autosomal dominant"
+BMGC_DS10000,BMG_DS037826,Noonan like syndrome
+BMGC_DS10001,BMG_DS037827,"Noduli Cutanei, Multiple, with Urinary Tract Abnormalities"
+BMGC_DS10002,BMG_DS037828,"Sick Sinus Syndrome 2, Autosomal Dominant"
+BMGC_DS10003,BMG_DS037829,Hypertension Resistant to Conventional Therapy
+BMGC_DS10004,BMG_DS037832,"Neuropathy, congenital, with arthrogryposis multiplex"
+BMGC_DS10005,BMG_DS037833,"Ceroid Lipofuscinosis, Neuronal, Parry Type"
+BMGC_DS10006,BMG_DS037837,"NEUROFIBROMATOSIS, FAMILIAL SPINAL"
+BMGC_DS10007,BMG_DS037838,"AMYOTROPHY, HEREDITARY NEURALGIC"
+BMGC_DS10008,BMG_DS037839,RETINITIS PIGMENTOSA 27
+BMGC_DS10009,BMG_DS037840,"Retinal Degeneration, Autosomal Recessive, Clumped Pigment Type"
+BMGC_DS10010,BMG_DS037841,Van der Woude syndrome
+BMGC_DS10011,BMG_DS037842,"Necrotizing Encephalomyelopathy, Subacute, of Leigh, Adult"
+BMGC_DS10012,BMG_DS037843,"NASAL HYPERPIGMENTATION, FAMILIAL TRANSVERSE"
+BMGC_DS10013,BMG_DS037844,"NASAL GROOVE, FAMILIAL TRANSVERSE"
+BMGC_DS10014,BMG_DS037845,"Nasal Alar Collapse, Bilateral"
+BMGC_DS10015,BMG_DS037846,Narcolepsy 1
+BMGC_DS10016,BMG_DS037850,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10"
+BMGC_DS10017,BMG_DS037851,"CARDIOMYOPATHY, DILATED, 1S"
+BMGC_DS10018,BMG_DS037852,Sheldon-hall syndrome
+BMGC_DS10019,BMG_DS037853,Myopia 2
+BMGC_DS10020,BMG_DS037854,Myopathy with Storage of Glycoproteins and Glycosaminoglycans
+BMGC_DS10021,BMG_DS037856,"Myopathy, Centronuclear, Autosomal Dominant"
+BMGC_DS10022,BMG_DS037857,"Continuous Muscle Fiber Activity, Hereditary"
+BMGC_DS10023,BMG_DS037858,"Myoglobinuria, Autosomal Dominant"
+BMGC_DS10024,BMG_DS037859,Jankovic Rivera syndrome
+BMGC_DS10025,BMG_DS037860,Myoclonic dystonia
+BMGC_DS10026,BMG_DS037861,"Myoclonus, Cerebellar Ataxia, and Deafness"
+BMGC_DS10027,BMG_DS037863,"Myoclonic Epilepsy, Hartung Type"
+BMGC_DS10028,BMG_DS037864,transient myeloproliferative syndrome
+BMGC_DS10029,BMG_DS037865,myelinated optic nerve fibers
+BMGC_DS10030,BMG_DS037866,"Myasthenia, Limb-Girdle, Autoimmune"
+BMGC_DS10031,BMG_DS037868,"Muscular Dystrophy, Pseudohypertrophic, With Internalized Capillaries"
+BMGC_DS10032,BMG_DS037870,"Muscular dystrophy, limb-girdle, type 1A"
+BMGC_DS10033,BMG_DS037871,facioscapulohumeral muscular dystrophy 2
+BMGC_DS10034,BMG_DS037872,Facioscapulohumeral muscular dystrophy 1a
+BMGC_DS10035,BMG_DS037873,BETHLEM MYOPATHY 1
+BMGC_DS10036,BMG_DS037874,"Muscular Dystrophy, Barnes Type"
+BMGC_DS10037,BMG_DS037875,"Muscular Atrophy, Malignant Neurogenic"
+BMGC_DS10038,BMG_DS037876,"Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant"
+BMGC_DS10039,BMG_DS037877,"neuronopathy, distal hereditary motor, type 2A"
+BMGC_DS10040,BMG_DS037878,"Neuropathy, Distal Hereditary Motor, Type VIIA"
+BMGC_DS10041,BMG_DS037879,"Muscle Cramps, Familial"
+BMGC_DS10042,BMG_DS037880,CEREBELLOPARENCHYMAL DISORDER VI
+BMGC_DS10043,BMG_DS037883,Multiple Exostoses with Spastic Tetraparesis
+BMGC_DS10044,BMG_DS037884,NONDISJUNCTION
+BMGC_DS10045,BMG_DS037885,"CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV"
+BMGC_DS10046,BMG_DS037886,Monophalangy of Great Toe
+BMGC_DS10047,BMG_DS037889,Macrosomia obesity macrocephaly ocular abnormalities
+BMGC_DS10048,BMG_DS037890,MYXOMATOUS MITRAL VALVE PROLAPSE 1
+BMGC_DS10049,BMG_DS037891,METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS
+BMGC_DS10050,BMG_DS037892,"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1"
+BMGC_DS10051,BMG_DS037894,mirror movements 1
+BMGC_DS10052,BMG_DS037896,Holoprosencephaly 2
+BMGC_DS10053,BMG_DS037899,"Microphthalmia, Isolated, With Corectopia"
+BMGC_DS10054,BMG_DS037900,"Microphthalmia, Isolated, with Cataract 1"
+BMGC_DS10055,BMG_DS037901,Cloverleaf skull micromelia thoracic dysplasia
+BMGC_DS10056,BMG_DS037903,"Microcornea, glaucoma, and absent frontal sinuses"
+BMGC_DS10057,BMG_DS037904,"Metatarsus Varus, Type I"
+BMGC_DS10058,BMG_DS037905,Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly
+BMGC_DS10059,BMG_DS037908,"MESOMELIC DYSPLASIA, KANTAPUTRA TYPE"
+BMGC_DS10060,BMG_DS037910,"Meralgia Paraesthetica, Familial"
+BMGC_DS10061,BMG_DS037911,Mental and Growth Retardation with Amblyopia
+BMGC_DS10062,BMG_DS037912,"Membranous Cranial Ossification, Delayed"
+BMGC_DS10063,BMG_DS037915,melanoma and neural system tumor syndrome
+BMGC_DS10064,BMG_DS037916,"melanoma, malignant familial intraocular"
+BMGC_DS10065,BMG_DS037917,"melanoma, cutaneous malignant, susceptibility to, 2"
+BMGC_DS10066,BMG_DS037918,"melanoma, cutaneous malignant, susceptibility to, 1"
+BMGC_DS10067,BMG_DS037920,mediosternal depigmentation line
+BMGC_DS10068,BMG_DS037922,"Median cleft lip, corpus callosum, lipoma, and skin polyps"
+BMGC_DS10069,BMG_DS037923,Maxillofacial Dysostosis
+BMGC_DS10070,BMG_DS037926,"Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type"
+BMGC_DS10071,BMG_DS037927,malocclusion due to protuberant upper front teeth
+BMGC_DS10072,BMG_DS037930,"Hypomagnesemia 2, renal"
+BMGC_DS10073,BMG_DS037932,"Macular Dystrophy, Fenestrated Sheen Type"
+BMGC_DS10074,BMG_DS037933,"MACULAR DYSTROPHY, ATYPICAL VITELLIFORM"
+BMGC_DS10075,BMG_DS037934,"MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1"
+BMGC_DS10076,BMG_DS037935,"psoriatic arthritis, susceptibility to"
+BMGC_DS10077,BMG_DS037936,"Lymphedema, microcephaly and chorioretinopathy syndrome"
+BMGC_DS10078,BMG_DS037937,Lymphedema and Cerebral Arteriovenous Anomaly
+BMGC_DS10079,BMG_DS037939,"Lumbar Stenosis, Familial"
+BMGC_DS10080,BMG_DS037941,lithium transport
+BMGC_DS10081,BMG_DS037945,"Lp(A) Deficiency, Congenital"
+BMGC_DS10082,BMG_DS037947,lipoma of the conjunctiva
+BMGC_DS10083,BMG_DS037948,"Lip, Hamartomatous"
+BMGC_DS10084,BMG_DS037949,Median nodule of upper lip
+BMGC_DS10085,BMG_DS037950,LI-FRAUMENI SYNDROME 1
+BMGC_DS10086,BMG_DS037951,"Lichen Planus, Familial"
+BMGC_DS10087,BMG_DS037952,Levator-Medial Rectus Synkinesis
+BMGC_DS10088,BMG_DS037953,"Leukocyte Nuclear Appendages, Hereditary Prevalence of"
+BMGC_DS10089,BMG_DS037954,"hepatitis C virus, susceptibility to"
+BMGC_DS10090,BMG_DS037955,"Platyspondylic Lethal Skeletal Dysplasia, Torrance Type"
+BMGC_DS10091,BMG_DS037956,Leri pleonosteosis
+BMGC_DS10092,BMG_DS037957,"Lentiginosis, Centrofacial Neurodysraphic"
+BMGC_DS10093,BMG_DS037958,leiomyoma of vulva and esophagus
+BMGC_DS10094,BMG_DS037961,"Tooth Agenesis, Selective, 4"
+BMGC_DS10095,BMG_DS037962,"Succedaneous Teeth, Agenesis Of"
+BMGC_DS10096,BMG_DS037964,"Lactic Acidosis, Chronic Adult Form"
+BMGC_DS10097,BMG_DS037965,familial congenital nasolacrimal duct obstruction
+BMGC_DS10098,BMG_DS037966,"labia minora, incomplete adhesion of"
+BMGC_DS10099,BMG_DS037967,hereditary hyperekplexia
+BMGC_DS10100,BMG_DS037968,Keratosis focal palmoplantar gingival
+BMGC_DS10101,BMG_DS037969,Keratosis palmoplantaris papulosa
+BMGC_DS10102,BMG_DS037970,Keratosis Palmaris et Plantaris with Clinodactyly
+BMGC_DS10103,BMG_DS037971,palmoplantar keratoderma-esophageal carcinoma syndrome
+BMGC_DS10104,BMG_DS037972,Keratoderma palmoplantar spastic paralysis
+BMGC_DS10105,BMG_DS037973,Palmoplantar Keratoderma with Deafness
+BMGC_DS10106,BMG_DS037974,Keratoconus 1
+BMGC_DS10107,BMG_DS037975,Keratitis Fugax Hereditaria
+BMGC_DS10108,BMG_DS037976,"Keratitis, hereditary"
+BMGC_DS10109,BMG_DS037977,"cirrhosis, noncryptogenic, susceptibility to"
+BMGC_DS10110,BMG_DS037980,"kallikrein, decreased urinary activity of"
+BMGC_DS10111,BMG_DS037981,Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency
+BMGC_DS10112,BMG_DS037982,"Mitral Valve Prolapse, Myxomatous 3"
+BMGC_DS10113,BMG_DS037984,"FANCONI ANEMIA, COMPLEMENTATION GROUP N"
+BMGC_DS10114,BMG_DS037986,Holoprosencephaly 9
+BMGC_DS10115,BMG_DS037987,HOLOPROSENCEPHALY 7
+BMGC_DS10116,BMG_DS037988,congenital anomalies of kidney and urinary tract 1
+BMGC_DS10117,BMG_DS037989,Immunodeficiency due to Defect in MAPBP-Interacting Protein
+BMGC_DS10118,BMG_DS037990,"Epiphyseal Dysplasia, Baumann Type"
+BMGC_DS10119,BMG_DS037991,Mitochondrial Phosphate Carrier Deficiency
+BMGC_DS10120,BMG_DS037992,"Congenital Disorder Of Glycosylation, Type Im"
+BMGC_DS10121,BMG_DS037993,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11"
+BMGC_DS10122,BMG_DS037994,Alopecia-Mental Retardation Syndrome 2
+BMGC_DS10123,BMG_DS037995,"DEAFNESS, AUTOSOMAL RECESSIVE 68"
+BMGC_DS10124,BMG_DS037997,Cone-Rod Dystrophy 11
+BMGC_DS10125,BMG_DS037998,"West Nile virus, susceptibility to"
+BMGC_DS10126,BMG_DS038000,"Diabetes Mellitus, Transient Neonatal, 2"
+BMGC_DS10127,BMG_DS038001,"Diarrhea 4, Malabsorptive, Congenital"
+BMGC_DS10128,BMG_DS038002,Orofacial Cleft 9
+BMGC_DS10129,BMG_DS038003,Retinitis Pigmentosa 33
+BMGC_DS10130,BMG_DS038004,"Spastic Paraplegia 30, Autosomal Recessive"
+BMGC_DS10131,BMG_DS038005,Retinal Cone Dystrophy 3B
+BMGC_DS10132,BMG_DS038006,"Epilepsy, Nocturnal Frontal Lobe, Type 4"
+BMGC_DS10133,BMG_DS038007,Familial anomalous origin of right pulmonary artery
+BMGC_DS10134,BMG_DS038008,AICARDI-GOUTIERES SYNDROME 4
+BMGC_DS10135,BMG_DS038010,AICARDI-GOUTIERES SYNDROME 3
+BMGC_DS10136,BMG_DS038011,"systemic lupus erythematosus, susceptibility to, 6"
+BMGC_DS10137,BMG_DS038012,Aminoacylase 1 deficiency
+BMGC_DS10138,BMG_DS038013,Retinitis Pigmentosa 31
+BMGC_DS10139,BMG_DS038016,"Cardiomyopathy, Dilated, 1q"
+BMGC_DS10140,BMG_DS038017,Retinitis Pigmentosa 32
+BMGC_DS10141,BMG_DS038018,"CARDIOMYOPATHY, DILATED, 1P"
+BMGC_DS10142,BMG_DS038020,"ALPHA/BETA T-CELL LYMPHOPENIA WITH GAMMA/DELTA T-CELL EXPANSION, SEVERE CYTOMEGALOVIRUS INFECTION, AND AUTOIMMUNITY"
+BMGC_DS10143,BMG_DS038021,"leprosy, susceptibility to, 1"
+BMGC_DS10144,BMG_DS038022,"Glaucoma 1, Open Angle, G"
+BMGC_DS10145,BMG_DS038027,PARIETAL FORAMINA 3
+BMGC_DS10146,BMG_DS038029,Nanophthalmos 2
+BMGC_DS10147,BMG_DS038031,"Spastic Paraplegia, Optic Atrophy, and Neuropathy"
+BMGC_DS10148,BMG_DS038034,"Drug Metabolism, Poor, CYP2C19-Related"
+BMGC_DS10149,BMG_DS038035,"Deafness, Autosomal Recessive 23"
+BMGC_DS10150,BMG_DS038036,Immunoglobulin a deficiency 2
+BMGC_DS10151,BMG_DS038037,"Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome"
+BMGC_DS10152,BMG_DS038038,"Filaminopathy, autosomal dominant"
+BMGC_DS10153,BMG_DS038040,"Stickler Syndrome, Type I, Nonsyndromic Ocular"
+BMGC_DS10154,BMG_DS038041,"RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT"
+BMGC_DS10155,BMG_DS038042,LEFT VENTRICULAR NONCOMPACTION 2
+BMGC_DS10156,BMG_DS038045,Al-Gazali Syndrome
+BMGC_DS10157,BMG_DS038046,"SARCOIDOSIS, EARLY-ONSET"
+BMGC_DS10158,BMG_DS038047,Goldberg-Shprintzen megacolon syndrome
+BMGC_DS10159,BMG_DS038049,"Supranuclear Palsy, Progressive, 2"
+BMGC_DS10160,BMG_DS038050,"Myopathy, Myofibrillar, Zasp-Related"
+BMGC_DS10161,BMG_DS038051,Generalized Epilepsy and Paroxysmal Dyskinesia
+BMGC_DS10162,BMG_DS038052,"Chondrodysplasia, acromesomelic, with genital anomalies"
+BMGC_DS10163,BMG_DS038053,"DEAFNESS, AUTOSOMAL RECESSIVE 48"
+BMGC_DS10164,BMG_DS038054,"Mental retardation, keratoconus, febrile seizures, and sinoatrial block"
+BMGC_DS10165,BMG_DS038055,"Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction"
+BMGC_DS10166,BMG_DS038056,Tukel syndrome
+BMGC_DS10167,BMG_DS038057,susceptibility to HIV infection
+BMGC_DS10168,BMG_DS038058,Holoprosencephaly 8
+BMGC_DS10169,BMG_DS038059,Preeclampsia Eclampsia 4
+BMGC_DS10170,BMG_DS038064,"Cataract, Congenital Nuclear, Autosomal Recessive 1"
+BMGC_DS10171,BMG_DS038065,Epidermolysis Bullosa Simplex with Migratory Circinate Erythema
+BMGC_DS10172,BMG_DS038067,"Spastic Paraplegia 28, Autosomal Recessive"
+BMGC_DS10173,BMG_DS038068,Carotid Intimal Medial Thickness 1
+BMGC_DS10174,BMG_DS038071,"multiple epiphyseal dysplasia, with severe proximal femoral dysplasia"
+BMGC_DS10175,BMG_DS038072,Rhabdoid Tumor Predisposition Syndrome 1
+BMGC_DS10176,BMG_DS038073,Erythrokeratodermia Variabilis 3
+BMGC_DS10177,BMG_DS038074,"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H"
+BMGC_DS10178,BMG_DS038075,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"
+BMGC_DS10179,BMG_DS038076,SPINOCEREBELLAR ATAXIA 27
+BMGC_DS10180,BMG_DS038077,SPINOCEREBELLAR ATAXIA 26
+BMGC_DS10181,BMG_DS038079,"B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations"
+BMGC_DS10182,BMG_DS038080,Familial neurocardiogenic syncope
+BMGC_DS10183,BMG_DS038081,"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3"
+BMGC_DS10184,BMG_DS038082,Nemaline myopathy 4
+BMGC_DS10185,BMG_DS038083,Nemaline myopathy 1
+BMGC_DS10186,BMG_DS038084,"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2"
+BMGC_DS10187,BMG_DS038085,Nemaline myopathy 6
+BMGC_DS10188,BMG_DS038087,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7"
+BMGC_DS10189,BMG_DS038089,Li-Fraumeni Syndrome 2
+BMGC_DS10190,BMG_DS038090,"Stuttering, Familial Persistent 2"
+BMGC_DS10191,BMG_DS038091,"Charcot-Marie-Tooth Disease, Axonal, Type 2A2"
+BMGC_DS10192,BMG_DS038092,Myopia 10
+BMGC_DS10193,BMG_DS038093,Myopia 9
+BMGC_DS10194,BMG_DS038094,Myopia 8
+BMGC_DS10195,BMG_DS038095,Myopia 7
+BMGC_DS10196,BMG_DS038096,"febrile seizures, familial, 5"
+BMGC_DS10197,BMG_DS038097,Generalized onset tonic epileptic seizure
+BMGC_DS10198,BMG_DS038098,Senior-Loken Syndrome 5
+BMGC_DS10199,BMG_DS038099,"febrile seizures, familial, 6"
+BMGC_DS10200,BMG_DS038101,Alpha-N-acetylgalactosaminidase deficiency type 2
+BMGC_DS10201,BMG_DS038102,Alpha-N-acetylgalactosaminidase deficiency type 1
+BMGC_DS10202,BMG_DS038103,"GRISCELLI SYNDROME, TYPE 3"
+BMGC_DS10203,BMG_DS038104,"Spondyloepiphyseal Dysplasia Tarda, Autosomal Recessive, Leroy-Spranger Type"
+BMGC_DS10204,BMG_DS038105,Bruck syndrome 2
+BMGC_DS10205,BMG_DS038106,Foveal Hypoplasia and Anterior Segment Dysgenesis
+BMGC_DS10206,BMG_DS038107,Glucocorticoid Deficiency 3
+BMGC_DS10207,BMG_DS038108,"Spastic paraplegia 26, autosomal recessive"
+BMGC_DS10208,BMG_DS038109,Loeys-Dietz Aortic Aneurysm Syndrome
+BMGC_DS10209,BMG_DS038110,"Dissection, Ascending Aorta"
+BMGC_DS10210,BMG_DS038111,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If"
+BMGC_DS10211,BMG_DS038113,"Total Hypotrichosis, Mari type"
+BMGC_DS10212,BMG_DS038114,Branchiogenic-Deafness Syndrome
+BMGC_DS10213,BMG_DS038117,spondyloepiphyseal dysplasia with metatarsal shortening
+BMGC_DS10214,BMG_DS038118,"Striatal Degeneration, Autosomal Dominant"
+BMGC_DS10215,BMG_DS038120,"Pseudohyperkalemia, Familial, 2, due to Red Cell Leak"
+BMGC_DS10216,BMG_DS038121,"Hyperthyroidism, Nonautoimmune"
+BMGC_DS10217,BMG_DS038122,"malaria, mild, susceptibility to"
+BMGC_DS10218,BMG_DS038124,"Corneal Dystrophy, Posterior Polymorphous, 3"
+BMGC_DS10219,BMG_DS038125,"Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease"
+BMGC_DS10220,BMG_DS038126,autosomal dominant auditory neuropathy 1
+BMGC_DS10221,BMG_DS038127,"Arthrogryposis, Distal, Type 4"
+BMGC_DS10222,BMG_DS038128,"ANEURYSM, INTRACRANIAL BERRY, 3"
+BMGC_DS10223,BMG_DS038130,"Limb-Girdle Muscular Dystrophy, Type 1G"
+BMGC_DS10224,BMG_DS038131,"TELOMERE LENGTH, MEAN LEUKOCYTE"
+BMGC_DS10225,BMG_DS038132,PANCREATIC AND CEREBELLAR AGENESIS
+BMGC_DS10226,BMG_DS038133,Combined Oxidative Phosphorylation Deficiency 1
+BMGC_DS10227,BMG_DS038134,Nephropathy with Pretibial Epidermolysis Bullosa and Deafness
+BMGC_DS10228,BMG_DS038135,Amish Infantile Epilepsy Syndrome
+BMGC_DS10229,BMG_DS038136,Developmental regression
+BMGC_DS10230,BMG_DS038137,"Ceroid lipofuscinosis, neuronal 9"
+BMGC_DS10231,BMG_DS038138,"FANCONI ANEMIA, COMPLEMENTATION GROUP J"
+BMGC_DS10232,BMG_DS038139,"FANCONI ANEMIA, COMPLEMENTATION GROUP I"
+BMGC_DS10233,BMG_DS038140,"Spondylometaphyseal Dysplasia, Type A4"
+BMGC_DS10234,BMG_DS038141,Pierson syndrome
+BMGC_DS10235,BMG_DS038142,"melanoma, cutaneous malignant, susceptibility to, 3"
+BMGC_DS10236,BMG_DS038144,"Spastic Paraplegia 27, Autosomal Recessive"
+BMGC_DS10237,BMG_DS038145,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 9"
+BMGC_DS10238,BMG_DS038146,NARCOLEPSY 3
+BMGC_DS10239,BMG_DS038147,"Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature"
+BMGC_DS10240,BMG_DS038148,POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA
+BMGC_DS10241,BMG_DS038149,Emanuel syndrome
+BMGC_DS10242,BMG_DS038151,Peripheral Cone Dystrophy
+BMGC_DS10243,BMG_DS038152,Marfanoid Habitus with Situs Inversus
+BMGC_DS10244,BMG_DS038153,"DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT"
+BMGC_DS10245,BMG_DS038154,Premature Ovarian Failure 3
+BMGC_DS10246,BMG_DS038155,"dyslexia, susceptibility to, 8"
+BMGC_DS10247,BMG_DS038156,"Atrial Fibrillation, Familial, 3"
+BMGC_DS10248,BMG_DS038157,autosomal dominant sensory ataxia 1
+BMGC_DS10249,BMG_DS038158,"CATARACT, CONGENITAL, CERULEAN TYPE, 3"
+BMGC_DS10250,BMG_DS038159,Meacham syndrome
+BMGC_DS10251,BMG_DS038160,"Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive"
+BMGC_DS10252,BMG_DS038161,"Macular Dystrophy, Butterfly-Shaped Pigmentary, 2"
+BMGC_DS10253,BMG_DS038162,"CD8 Deficiency, Familial"
+BMGC_DS10254,BMG_DS038163,Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy
+BMGC_DS10255,BMG_DS038166,congenital myasthenic syndrome 4C
+BMGC_DS10256,BMG_DS038167,"Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency"
+BMGC_DS10257,BMG_DS038168,"Myasthenic Syndrome, Congenital, Fast-Channel"
+BMGC_DS10258,BMG_DS038169,Myopia 6
+BMGC_DS10259,BMG_DS038170,Alzheimer Disease 9
+BMGC_DS10260,BMG_DS038175,"Drug Metabolism, Poor, CYP2D6-Related"
+BMGC_DS10261,BMG_DS038176,"coronary heart disease, susceptibility to, 5"
+BMGC_DS10262,BMG_DS038177,"HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3"
+BMGC_DS10263,BMG_DS038178,"MACULAR DEGENERATION, AGE-RELATED, 3"
+BMGC_DS10264,BMG_DS038179,Waardenburg syndrome type 2D
+BMGC_DS10265,BMG_DS038180,"Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly"
+BMGC_DS10266,BMG_DS038181,OROFACIAL CLEFT 5
+BMGC_DS10267,BMG_DS038182,"orofacial cleft 6, susceptibility to"
+BMGC_DS10268,BMG_DS038183,isolated cleft palate
+BMGC_DS10269,BMG_DS038184,"Muscular Dystrophy, Congenital, Type 1D"
+BMGC_DS10270,BMG_DS038185,Carney Complex Variant
+BMGC_DS10271,BMG_DS038189,"MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 3"
+BMGC_DS10272,BMG_DS038191,"colorectal cancer, susceptibility to, 1"
+BMGC_DS10273,BMG_DS038193,Alpha-B Crystallinopathy
+BMGC_DS10274,BMG_DS038196,"transposition of the great arteries, dextro-looped"
+BMGC_DS10275,BMG_DS038197,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J"
+BMGC_DS10276,BMG_DS038198,"Leukodystrophy, Hypomyelinating, 2"
+BMGC_DS10277,BMG_DS038199,Sudden Infant Death with Dysgenesis of the Testes Syndrome
+BMGC_DS10278,BMG_DS038200,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie"
+BMGC_DS10279,BMG_DS038202,OTOSCLEROSIS 5
+BMGC_DS10280,BMG_DS038203,Pyruvate dehydrogenase phosphatase deficiency
+BMGC_DS10281,BMG_DS038205,SPINOCEREBELLAR ATAXIA 8
+BMGC_DS10282,BMG_DS038206,"scoliosis, isolated, susceptibility to, 3"
+BMGC_DS10283,BMG_DS038208,"epilepsy, idiopathic generalized, susceptibility to, 3"
+BMGC_DS10284,BMG_DS038209,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8"
+BMGC_DS10285,BMG_DS038210,Insulin-Like Growth Factor I Deficiency
+BMGC_DS10286,BMG_DS038212,"Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related"
+BMGC_DS10287,BMG_DS038214,"Microcephaly, Primary Autosomal Recessive, 5"
+BMGC_DS10288,BMG_DS038215,Spinocerebellar ataxia 25
+BMGC_DS10289,BMG_DS038219,AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency
+BMGC_DS10290,BMG_DS038220,SPINOCEREBELLAR ATAXIA 20
+BMGC_DS10291,BMG_DS038221,"Spondylocostal Dysostosis 2, Autosomal Recessive"
+BMGC_DS10292,BMG_DS038222,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L"
+BMGC_DS10293,BMG_DS038223,Robin Sequence with Distinctive Facial Appearance and Brachydactyly
+BMGC_DS10294,BMG_DS038226,"DEAFNESS, AUTOSOMAL RECESSIVE 32"
+BMGC_DS10295,BMG_DS038227,"Deafness, Autosomal Dominant 47"
+BMGC_DS10296,BMG_DS038228,ICHTHYOSIS PREMATURITY SYNDROME
+BMGC_DS10297,BMG_DS038229,"Ciliary Dyskinesia, Primary, 5"
+BMGC_DS10298,BMG_DS038231,"Deafness, Autosomal Dominant 31"
+BMGC_DS10299,BMG_DS038232,"CILIARY DYSKINESIA, PRIMARY, 3"
+BMGC_DS10300,BMG_DS038233,"Deafness, Autosomal Dominant 28"
+BMGC_DS10301,BMG_DS038234,"ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1"
+BMGC_DS10302,BMG_DS038235,"Spondyloepiphyseal dysplasia, Omani type"
+BMGC_DS10303,BMG_DS038236,Gross motor development delay
+BMGC_DS10304,BMG_DS038237,"ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2"
+BMGC_DS10305,BMG_DS038238,JOUBERT SYNDROME 3
+BMGC_DS10306,BMG_DS038239,Amyotrophic Lateral Sclerosis 8
+BMGC_DS10307,BMG_DS038240,"Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia"
+BMGC_DS10308,BMG_DS038241,"Hypertension, Diastolic, Resistance to"
+BMGC_DS10309,BMG_DS038242,oligodontia-cancer predisposition syndrome
+BMGC_DS10310,BMG_DS038243,MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY
+BMGC_DS10311,BMG_DS038245,"Charcot-Marie-Tooth disease, axonal, Type 2G"
+BMGC_DS10312,BMG_DS038248,"asthma-related traits, susceptibility to, 2"
+BMGC_DS10313,BMG_DS038249,"Atrial Fibrillation, Familial, 2"
+BMGC_DS10314,BMG_DS038251,Burn-Mckeown syndrome
+BMGC_DS10315,BMG_DS038253,Ulnar-Fibular Ray Defect and Brachydactyly
+BMGC_DS10316,BMG_DS038254,"CARDIOMYOPATHY, DILATED, 1O"
+BMGC_DS10317,BMG_DS038255,sick sinus syndrome 1
+BMGC_DS10318,BMG_DS038256,"DEAFNESS, AUTOSOMAL RECESSIVE 35"
+BMGC_DS10319,BMG_DS038259,"legionnaire disease, susceptibility to"
+BMGC_DS10320,BMG_DS038260,Leber Congenital Amaurosis 9
+BMGC_DS10321,BMG_DS038261,Larsen-Like Syndrome
+BMGC_DS10322,BMG_DS038262,SCHIZOPHRENIA 12
+BMGC_DS10323,BMG_DS038263,"Aneurysm, intracranial berry, 2"
+BMGC_DS10324,BMG_DS038264,"ERYTHROCYTOSIS, FAMILIAL, 2"
+BMGC_DS10325,BMG_DS038268,Myopia 5
+BMGC_DS10326,BMG_DS038269,"Corneal Dystrophy, Lattice Type IIIA"
+BMGC_DS10327,BMG_DS038270,Knobloch Syndrome Type II
+BMGC_DS10328,BMG_DS038273,"intellectual disability, autosomal recessive 3"
+BMGC_DS10329,BMG_DS038274,"Epilepsy, Nocturnal Frontal Lobe, Type 1"
+BMGC_DS10330,BMG_DS038275,Autosomal Dominant Lateral Temporal Lobe Epilepsy
+BMGC_DS10331,BMG_DS038276,schizophrenia 3
+BMGC_DS10332,BMG_DS038277,ABCD syndrome
+BMGC_DS10333,BMG_DS038278,maturity-onset diabetes of the young type 3
+BMGC_DS10334,BMG_DS038279,"malignant hyperthermia, susceptibility to, 4"
+BMGC_DS10335,BMG_DS038280,MITOCHONDRIAL MYOPATHY AND SIDEROBLASTIC ANEMIA
+BMGC_DS10336,BMG_DS038283,"Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly"
+BMGC_DS10337,BMG_DS038284,Arterial Dissection with Lentiginosis
+BMGC_DS10338,BMG_DS038285,"Hypertrichosis, anterior cervical"
+BMGC_DS10339,BMG_DS038286,Angiokeratoma Corporis Diffusum with Arteriovenous Fistulas
+BMGC_DS10340,BMG_DS038288,"Aphalangia, Partial, with Syndactyly and Duplication of Metatarsal IV"
+BMGC_DS10341,BMG_DS038289,Mesomelia-synostoses syndrome
+BMGC_DS10342,BMG_DS038290,"telangiectasia, hereditary hemorrhagic, type 2"
+BMGC_DS10343,BMG_DS038291,CODAS syndrome
+BMGC_DS10344,BMG_DS038292,cone-rod dystrophy 14
+BMGC_DS10345,BMG_DS038293,"Spastic paraplegia 6, autosomal dominant"
+BMGC_DS10346,BMG_DS038294,Aplasia cutis congenita of limbs recessive
+BMGC_DS10347,BMG_DS038295,"Pachydermodactyly, Familial"
+BMGC_DS10348,BMG_DS038296,"SPINAL MUSCULAR ATROPHY, TYPE IV"
+BMGC_DS10349,BMG_DS038298,Band Heterotopia of Brain
+BMGC_DS10350,BMG_DS038300,Succinic Acidemia
+BMGC_DS10351,BMG_DS038301,"TIBIAL MUSCULAR DYSTROPHY, TARDIVE"
+BMGC_DS10352,BMG_DS038303,RIPPLING MUSCLE DISEASE 1
+BMGC_DS10353,BMG_DS038304,PARC syndrome
+BMGC_DS10354,BMG_DS038306,Osteopetrosis and infantile neuroaxonal dystrophy
+BMGC_DS10355,BMG_DS038308,"DIABETES MELLITUS, INSULIN-DEPENDENT, 5"
+BMGC_DS10356,BMG_DS038311,"Deafness, Autosomal Recessive 3"
+BMGC_DS10357,BMG_DS038312,"Epiphyseal dysplasia, multiple, 1"
+BMGC_DS10358,BMG_DS038317,"Polycystic kidneys, severe infantile with tuberous sclerosis"
+BMGC_DS10359,BMG_DS038318,Lopes Gorlin syndrome
+BMGC_DS10360,BMG_DS038319,APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS
+BMGC_DS10361,BMG_DS038320,"HELICOBACTER PYLORI INFECTION, SUSCEPTIBILITY TO"
+BMGC_DS10362,BMG_DS038321,"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4"
+BMGC_DS10363,BMG_DS038322,Bor-Duane hydrocephalus contiguous gene syndrome
+BMGC_DS10364,BMG_DS038323,"Hydrocephalus, Autosomal Dominant"
+BMGC_DS10365,BMG_DS038324,Oculomaxillofacial dysostosis
+BMGC_DS10366,BMG_DS038325,"Diffuse palmoplantar keratoderma, Bothnian type"
+BMGC_DS10367,BMG_DS038326,"Exostoses, Multiple, Type III"
+BMGC_DS10368,BMG_DS038327,"Epiphyseal dysplasia, multiple, 2"
+BMGC_DS10369,BMG_DS038328,"dyslexia, susceptibility to, 2"
+BMGC_DS10370,BMG_DS038329,multiple cutaneous and mucosal venous malformations
+BMGC_DS10371,BMG_DS038330,ICHTHYOSIS EXFOLIATIVA
+BMGC_DS10372,BMG_DS038331,Waardenburg syndrome type 2B
+BMGC_DS10373,BMG_DS038332,"FANCONI ANEMIA, COMPLEMENTATION GROUP D1"
+BMGC_DS10374,BMG_DS038333,Kuzniecky syndrome
+BMGC_DS10375,BMG_DS038334,"Spinal Muscular Atrophy, Distal, Congenital Nonprogressive"
+BMGC_DS10376,BMG_DS038335,"Hyperparathyroidism, Primary, Caused By Water Clear Cell Hyperplasia"
+BMGC_DS10377,BMG_DS038336,NANOPHTHALMOS 1
+BMGC_DS10378,BMG_DS038337,"CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE"
+BMGC_DS10379,BMG_DS038338,MELANOMA-PANCREATIC CANCER SYNDROME
+BMGC_DS10380,BMG_DS038340,"Hirschsprung disease, susceptibility to, 2"
+BMGC_DS10381,BMG_DS038341,Sacral defect and anterior sacral meningocele
+BMGC_DS10382,BMG_DS038342,"CEROID LIPOFUSCINOSIS, NEURONAL, 8"
+BMGC_DS10383,BMG_DS038343,"Ceroid Lipofuscinosis, Neuronal, 7"
+BMGC_DS10384,BMG_DS038344,Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
+BMGC_DS10385,BMG_DS038345,Retinitis Pigmentosa 11
+BMGC_DS10386,BMG_DS038346,Retinitis Pigmentosa 14
+BMGC_DS10387,BMG_DS038347,"epilepsy, childhood absence, susceptibility to, 1"
+BMGC_DS10388,BMG_DS038351,"Rhizomelic chondrodysplasia punctata, type 3"
+BMGC_DS10389,BMG_DS038352,WARBURG MICRO SYNDROME 1
+BMGC_DS10390,BMG_DS038353,"Dysphasia, Familial Developmental"
+BMGC_DS10391,BMG_DS038354,Stargardt disease 3
+BMGC_DS10392,BMG_DS038355,Retinitis Pigmentosa 12
+BMGC_DS10393,BMG_DS038356,SPLIT-HAND/FOOT MALFORMATION 3
+BMGC_DS10394,BMG_DS038357,Spondyloepiphyseal Dysplasia Tarda with Characteristic Facies
+BMGC_DS10395,BMG_DS038358,Nivelon Nivelon Mabille syndrome
+BMGC_DS10396,BMG_DS038359,Pancreatic beta cell agenesis with neonatal diabetes mellitus
+BMGC_DS10397,BMG_DS038360,"Macrocytosis, Familial"
+BMGC_DS10398,BMG_DS038361,"Vitamin D Hydroxylation-Deficient Rickets, Type 1B"
+BMGC_DS10399,BMG_DS038362,familial chronic myelocytic leukemia-like syndrome
+BMGC_DS10400,BMG_DS038363,"DEAFNESS, AUTOSOMAL RECESSIVE 2"
+BMGC_DS10401,BMG_DS038364,Retinitis Pigmentosa 13
+BMGC_DS10402,BMG_DS038365,Bladder Exstrophy and Epispadias Complex
+BMGC_DS10403,BMG_DS038366,Eiken Skeletal Dysplasia
+BMGC_DS10404,BMG_DS038368,"Wolfram Syndrome, Mitochondrial Form"
+BMGC_DS10405,BMG_DS038369,"DEAFNESS, AMINOGLYCOSIDE-INDUCED"
+BMGC_DS10406,BMG_DS038370,"Parkinson Disease, Mitochondrial"
+BMGC_DS10407,BMG_DS038372,"MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE"
+BMGC_DS10408,BMG_DS038373,"myoglobinuria, recurrent"
+BMGC_DS10409,BMG_DS038376,"ATAXIA AND POLYNEUROPATHY, ADULT-ONSET"
+BMGC_DS10410,BMG_DS038377,LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
+BMGC_DS10411,BMG_DS038378,MITOCHONDRIAL COMPLEX I DEFICIENCY
+BMGC_DS10412,BMG_DS038379,chloramphenicol toxicity
+BMGC_DS10413,BMG_DS038380,"Alzheimer disease, susceptibility to, mitochondrial"
+BMGC_DS10414,BMG_DS038384,"Striatonigral Degeneration, Infantile, Mitochondrial"
+BMGC_DS10415,BMG_DS038385,Mitochondrial Myopathy with Diabetes
+BMGC_DS10416,BMG_DS038386,LEBER OPTIC ATROPHY AND DYSTONIA
+BMGC_DS10417,BMG_DS038388,"Hairy Ears, Y-Linked"
+BMGC_DS10418,BMG_DS038389,"Spermatogenic Failure, Nonobstructive, Y-Linked"
+BMGC_DS10419,BMG_DS038394,"Retinitis Pigmentosa, Y-Linked"
+BMGC_DS10420,BMG_DS038396,"intellectual disability, X-linked 89"
+BMGC_DS10421,BMG_DS038399,"Von Willebrand Disease, X-Linked Form"
+BMGC_DS10422,BMG_DS038400,"Vesicoureteral Reflux, X-Linked"
+BMGC_DS10423,BMG_DS038401,UNIQUE GREEN PHENOMENON
+BMGC_DS10424,BMG_DS038403,Say Meyer syndrome
+BMGC_DS10425,BMG_DS038404,Torticollis keloids cryptorchidism renal dysplasia
+BMGC_DS10426,BMG_DS038405,"Dystonia 3, Torsion, X-Linked"
+BMGC_DS10427,BMG_DS038406,Thyroxine-Binding Globulin Deficiency
+BMGC_DS10428,BMG_DS038407,"Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis"
+BMGC_DS10429,BMG_DS038408,Thrombocytopenia with Elevated Serum Iga and Renal Disease
+BMGC_DS10430,BMG_DS038409,Thrombocytopenia 1
+BMGC_DS10431,BMG_DS038412,"Taurodontism, microdontia, and dens invaginatus"
+BMGC_DS10432,BMG_DS038414,SPLIT-HAND/FOOT MALFORMATION 2
+BMGC_DS10433,BMG_DS038415,"Bulbo-Spinal Atrophy, X-Linked"
+BMGC_DS10434,BMG_DS038416,"spatial visualization, aptitude for"
+BMGC_DS10435,BMG_DS038417,"Spastic paraplegia 2, X-linked"
+BMGC_DS10436,BMG_DS038419,Schimke X-linked mental retardation syndrome
+BMGC_DS10437,BMG_DS038420,SCARF syndrome
+BMGC_DS10438,BMG_DS038422,Retinitis Pigmentosa 6
+BMGC_DS10439,BMG_DS038423,Radiation Sensitivity of Natural Killer Activity
+BMGC_DS10440,BMG_DS038424,Radius absent anogenital anomalies
+BMGC_DS10441,BMG_DS038425,Pyruvate Dehydrogenase E1 Alpha Deficiency
+BMGC_DS10442,BMG_DS038426,Chronic lactic acidosis
+BMGC_DS10443,BMG_DS038427,"Multiple Pterygium Syndrome, X-Linked"
+BMGC_DS10444,BMG_DS038428,"PROPERDIN DEFICIENCY, X-LINKED"
+BMGC_DS10445,BMG_DS038429,"Properdin Deficiency, Type II"
+BMGC_DS10446,BMG_DS038430,"Properdin Deficiency, Type III"
+BMGC_DS10447,BMG_DS038431,TARP syndrome
+BMGC_DS10448,BMG_DS038434,Jensen syndrome
+BMGC_DS10449,BMG_DS038435,Optic Atrophy Spastic Paraplegia Syndrome
+BMGC_DS10450,BMG_DS038436,"CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5"
+BMGC_DS10451,BMG_DS038437,Early-onset X-linked optic atrophy
+BMGC_DS10452,BMG_DS038438,"Ophthalmoplegia, External, and Myopia"
+BMGC_DS10453,BMG_DS038440,"Nystagmus, Myoclonic"
+BMGC_DS10454,BMG_DS038441,"Nystagmus 1, congenital, X- linked"
+BMGC_DS10455,BMG_DS038443,"Neuropathy, Hereditary Sensory, X-Linked"
+BMGC_DS10456,BMG_DS038445,"MYOPIA 1, X-LINKED"
+BMGC_DS10457,BMG_DS038446,X-linked myopathy with excessive autophagy
+BMGC_DS10458,BMG_DS038447,MYELOLYMPHATIC INSUFFICIENCY
+BMGC_DS10459,BMG_DS038450,"Muscular Dystrophy, Hemizygous Lethal Type"
+BMGC_DS10460,BMG_DS038451,"Modifier, X-Linked, for Neurofunctional Defects"
+BMGC_DS10461,BMG_DS038454,METACARPAL 4-5 FUSION
+BMGC_DS10462,BMG_DS038455,Skeletal dysplasia with intellectual disability syndrome
+BMGC_DS10463,BMG_DS038456,Prieto syndrome
+BMGC_DS10464,BMG_DS038457,Wieacker-Wolff syndrome
+BMGC_DS10465,BMG_DS038458,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, WILSON-TURNER TYPE"
+BMGC_DS10466,BMG_DS038459,FRAGILE X TREMOR/ATAXIA SYNDROME
+BMGC_DS10467,BMG_DS038460,syndromic X-linked intellectual disability 12
+BMGC_DS10468,BMG_DS038461,Noncompaction cardiomyopathy
+BMGC_DS10469,BMG_DS038462,major affective disorder 2
+BMGC_DS10470,BMG_DS038463,"Male Pseudohermaphroditism due to Deficiency of Testicular 17,20-Desmolase"
+BMGC_DS10471,BMG_DS038464,"SPERMATOGENIC FAILURE, X-LINKED, 2"
+BMGC_DS10472,BMG_DS038465,"Macular Dystrophy, X-Linked"
+BMGC_DS10473,BMG_DS038466,Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis
+BMGC_DS10474,BMG_DS038467,Lesch-Nyhan phenotype with normal HGPRT
+BMGC_DS10475,BMG_DS038468,"Leiomyomatosis, esophageal and vulval, with nephropathy"
+BMGC_DS10476,BMG_DS038470,"Leber optic atrophy, susceptibility to"
+BMGC_DS10477,BMG_DS038471,"CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED"
+BMGC_DS10478,BMG_DS038472,Keratosis follicularis dwarfism cerebral atrophy
+BMGC_DS10479,BMG_DS038473,Spastic paraplegia with Kallmann syndrome
+BMGC_DS10480,BMG_DS038474,"Jaundice, Familial Obstructive, of Infancy"
+BMGC_DS10481,BMG_DS038475,IRIS HYPOPLASIA WITH GLAUCOMA
+BMGC_DS10482,BMG_DS038477,"impacted teeth, multiple"
+BMGC_DS10483,BMG_DS038479,"Immunodeficiency, X-Linked, with Deficiency of 115,000 Dalton Surface Glycoprotein"
+BMGC_DS10484,BMG_DS038480,Ichthyosis follicularis atrichia photophobia syndrome
+BMGC_DS10485,BMG_DS038483,SMALL PATELLA SYNDROME
+BMGC_DS10486,BMG_DS038484,"Internal Carotid Artery, Spontaneous Dissection of"
+BMGC_DS10487,BMG_DS038485,"iris pigment layer, cleavage of"
+BMGC_DS10488,BMG_DS038487,"insect Stings, hypersensitivity to"
+BMGC_DS10489,BMG_DS038490,"incisors, rotation of upper central"
+BMGC_DS10490,BMG_DS038492,solitary median maxillary central incisor syndrome
+BMGC_DS10491,BMG_DS038494,"IgE RESPONSIVENESS, ATOPIC"
+BMGC_DS10492,BMG_DS038495,IMMUNE SUPPRESSION
+BMGC_DS10493,BMG_DS038497,"Immune Deficiency, Familial Variable"
+BMGC_DS10494,BMG_DS038498,ICHTHYOSIS--CHEEK--EYEBROW SYNDROME
+BMGC_DS10495,BMG_DS038499,LEBER CONGENITAL AMAUROSIS 11
+BMGC_DS10496,BMG_DS038500,"Ichthyosis hystrix, Curth Macklin type"
+BMGC_DS10497,BMG_DS038502,Hypotrichosis Simplex of Scalp
+BMGC_DS10498,BMG_DS038503,HYPOPHOSPHATEMIC BONE DISEASE
+BMGC_DS10499,BMG_DS038504,Odontohypophosphatasia
+BMGC_DS10500,BMG_DS038505,Barakat syndrome
+BMGC_DS10501,BMG_DS038507,Hypomelia mullerian duct anomalies
+BMGC_DS10502,BMG_DS038508,"Hypocalciuric hypercalcemia, familial, type 2"
+BMGC_DS10503,BMG_DS038510,Hypertrophia Musculorum Vera
+BMGC_DS10504,BMG_DS038511,Ambras syndrome
+BMGC_DS10505,BMG_DS038512,"THYROID HORMONE RESISTANCE, SELECTIVE PITUITARY"
+BMGC_DS10506,BMG_DS038513,King Denborough syndrome
+BMGC_DS10507,BMG_DS038514,"Hyperthermia, Cutaneous, With Headaches And Nausea"
+BMGC_DS10508,BMG_DS038515,Hypertaurinuric Cardiomyopathy
+BMGC_DS10509,BMG_DS038516,Familial hypersensitivity pneumonitis
+BMGC_DS10510,BMG_DS038519,"Pseudohypoaldosteronism, Type IIa"
+BMGC_DS10511,BMG_DS038520,"Pseudohypoaldosteronism, Type IIb"
+BMGC_DS10512,BMG_DS038521,"Pseudohypoaldosteronism, Type IIc"
+BMGC_DS10513,BMG_DS038522,"hyperpigmentation with or without hypopigmentation, familial progressive"
+BMGC_DS10514,BMG_DS038523,Hyperpigmentation of Fuldauer and Kuijpers
+BMGC_DS10515,BMG_DS038525,HYPERPARATHYROIDISM 1
+BMGC_DS10516,BMG_DS038527,Hyperostosis Cranialis Interna
+BMGC_DS10517,BMG_DS038528,"Hyperlipoproteinemia, Type II, and Deafness"
+BMGC_DS10518,BMG_DS038529,"Palmoplantar Keratoderma, Epidermolytic, with Knuckle Pads"
+BMGC_DS10519,BMG_DS038532,isolated hyperchlorhidrosis
+BMGC_DS10520,BMG_DS038533,"Orthostatic Hypotensive Disorder, Streeten Type"
+BMGC_DS10521,BMG_DS038534,"MULTICYSTIC RENAL DYSPLASIA, BILATERAL"
+BMGC_DS10522,BMG_DS038535,Hyaloideoretinal degeneration of Wagner
+BMGC_DS10523,BMG_DS038536,"Horner Syndrome, Congenital"
+BMGC_DS10524,BMG_DS038537,Holoprosencephaly 4
+BMGC_DS10525,BMG_DS038538,HOLOPROSENCEPHALY 3
+BMGC_DS10526,BMG_DS038540,"Hidradenitis suppurativa, familial"
+BMGC_DS10527,BMG_DS038541,"HIP DYSPLASIA, BEUKES TYPE"
+BMGC_DS10528,BMG_DS038542,"Histiocytosis, Progressive Mucinous"
+BMGC_DS10529,BMG_DS038543,diaphragmatic hernia 1
+BMGC_DS10530,BMG_DS038544,"Hepatic Adenomas, Familial"
+BMGC_DS10531,BMG_DS038545,HEMOGLOBIN--VARIANTS FOR WHICH THE CHAIN CARRYING THE MUTATION IS UNKNOWN OR UNCERTAIN
+BMGC_DS10532,BMG_DS038548,"Methemoglobinemia, Alpha-Globin Type"
+BMGC_DS10533,BMG_DS038552,"Hemifacial Spasm, Familial"
+BMGC_DS10534,BMG_DS038553,Hemifacial Hyperplasia With Strabismus
+BMGC_DS10535,BMG_DS038554,Heme Oxygenase 1 Deficiency
+BMGC_DS10536,BMG_DS038555,hemangiomas of small intestine
+BMGC_DS10537,BMG_DS038556,"Heart-hand syndrome, Spanish type"
+BMGC_DS10538,BMG_DS038557,"Progressive Familial Heart Block, Type II"
+BMGC_DS10539,BMG_DS038559,Hand foot uterus syndrome
+BMGC_DS10540,BMG_DS038563,hairy palms and soles
+BMGC_DS10541,BMG_DS038564,hairy nose tip
+BMGC_DS10542,BMG_DS038566,ACHROMATOPSIA 4
+BMGC_DS10543,BMG_DS038567,"Prolonged Bleeding Time, Brachydactyly, and Mental Retardation"
+BMGC_DS10544,BMG_DS038571,Grant syndrome
+BMGC_DS10545,BMG_DS038578,Glucocorticoid Receptor Deficiency
+BMGC_DS10546,BMG_DS038579,"Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance"
+BMGC_DS10547,BMG_DS038580,GLOMUVENOUS MALFORMATIONS
+BMGC_DS10548,BMG_DS038583,Globulin Anomaly involving Beta (2A)-Globulin
+BMGC_DS10549,BMG_DS038584,Glaucoma and Sleep Apnea
+BMGC_DS10550,BMG_DS038585,"GLAUCOMA 1, OPEN ANGLE, E"
+BMGC_DS10551,BMG_DS038586,"GLAUCOMA 1, OPEN ANGLE, A"
+BMGC_DS10552,BMG_DS038588,"IRIDOGONIODYSGENESIS, TYPE 2"
+BMGC_DS10553,BMG_DS038589,Giant Platelet Syndrome with Thrombocytopenia
+BMGC_DS10554,BMG_DS038590,large congenital melanocytic nevus
+BMGC_DS10555,BMG_DS038591,GIANT NEUTROPHIL LEUKOCYTES
+BMGC_DS10556,BMG_DS038596,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F"
+BMGC_DS10557,BMG_DS038597,bradyopsia
+BMGC_DS10558,BMG_DS038599,Platelet Glycoprotein IV Deficiency
+BMGC_DS10559,BMG_DS038600,"Deafness, Autosomal Dominant 43"
+BMGC_DS10560,BMG_DS038601,"Microcephaly, Primary Autosomal Recessive, 6"
+BMGC_DS10561,BMG_DS038604,Branchiootic Syndrome 3
+BMGC_DS10562,BMG_DS038605,Retinitis Pigmentosa 26
+BMGC_DS10563,BMG_DS038606,"Deafness, Autosomal Dominant 49"
+BMGC_DS10564,BMG_DS038607,Orofacial Cleft 4
+BMGC_DS10565,BMG_DS038608,"spondyloepiphyseal dysplasia, Kimberley type"
+BMGC_DS10566,BMG_DS038609,Myosin storage myopathy
+BMGC_DS10567,BMG_DS038610,Capillary Malformation-Arteriovenous Malformation
+BMGC_DS10568,BMG_DS038611,"Nystagmus 3, congenital, autosomal dominant"
+BMGC_DS10569,BMG_DS038612,"Charcot-Marie-Tooth Disease, Recessive Intermediate A"
+BMGC_DS10570,BMG_DS038613,"Charcot-Marie-Tooth Disease, Dominant Intermediate C"
+BMGC_DS10571,BMG_DS038614,"CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1"
+BMGC_DS10572,BMG_DS038621,"Deafness, Autosomal Recessive 39"
+BMGC_DS10573,BMG_DS038622,"Deafness, Autosomal Recessive 40"
+BMGC_DS10574,BMG_DS038623,"Mandibulofacial Dysostosis with Ptosis, Autosomal Dominant"
+BMGC_DS10575,BMG_DS038624,OTOSCLEROSIS 3
+BMGC_DS10576,BMG_DS038625,"Slowed Nerve Conduction Velocity, Autosomal Dominant"
+BMGC_DS10577,BMG_DS038626,HERMANSKY-PUDLAK SYNDROME 2
+BMGC_DS10578,BMG_DS038627,"Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation"
+BMGC_DS10579,BMG_DS038628,"Deafness, Autosomal Dominant 41"
+BMGC_DS10580,BMG_DS038630,"DEAFNESS, AUTOSOMAL RECESSIVE 38"
+BMGC_DS10581,BMG_DS038631,"Epilepsy, Benign Neonatal, 3"
+BMGC_DS10582,BMG_DS038632,Neutrophil Immunodeficiency Syndrome
+BMGC_DS10583,BMG_DS038633,TROPICAL CALCIFIC PANCREATITIS
+BMGC_DS10584,BMG_DS038634,"IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 4"
+BMGC_DS10585,BMG_DS038635,Synpolydactyly 2
+BMGC_DS10586,BMG_DS038637,"autoimmune thyroid disease, susceptibility to, 3"
+BMGC_DS10587,BMG_DS038640,CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL
+BMGC_DS10588,BMG_DS038642,Nablus mask-like facial syndrome
+BMGC_DS10589,BMG_DS038643,"Lipodystrophy, Generalized, with Mental Retardation, Deafness, Short Stature, and Slender Bones"
+BMGC_DS10590,BMG_DS038645,Retinitis Pigmentosa 7
+BMGC_DS10591,BMG_DS038646,"Zinc Deficiency, Neonatal, due to Low Breast Milk Zinc"
+BMGC_DS10592,BMG_DS038647,"Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp"
+BMGC_DS10593,BMG_DS038648,Dystonia 18
+BMGC_DS10594,BMG_DS038649,Limb-girdle muscle atrophy
+BMGC_DS10595,BMG_DS038651,"Heterotopia, Periventricular, Autosomal Recessive"
+BMGC_DS10596,BMG_DS038653,JOUBERT SYNDROME 2
+BMGC_DS10597,BMG_DS038654,"Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux"
+BMGC_DS10598,BMG_DS038655,SCHIZOPHRENIA 11
+BMGC_DS10599,BMG_DS038657,"autism, susceptibility to, 3"
+BMGC_DS10600,BMG_DS038662,"Spinocerebellar ataxia, autosomal recessive 6"
+BMGC_DS10601,BMG_DS038664,Pontocerebellar Hypoplasia Type 3
+BMGC_DS10602,BMG_DS038665,Diaphanospondylodysostosis
+BMGC_DS10603,BMG_DS038666,"GAUCHER DISEASE, PERINATAL LETHAL"
+BMGC_DS10604,BMG_DS038671,SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION
+BMGC_DS10605,BMG_DS038672,Atrial septal defect 2
+BMGC_DS10606,BMG_DS038673,"Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like"
+BMGC_DS10607,BMG_DS038674,RETINITIS PIGMENTOSA 30
+BMGC_DS10608,BMG_DS038675,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii"
+BMGC_DS10609,BMG_DS038676,HYPOTRICHOSIS 6
+BMGC_DS10610,BMG_DS038677,"epilepsy, familial adult myoclonic, 2"
+BMGC_DS10611,BMG_DS038678,Chromosome 1p36 Deletion Syndrome
+BMGC_DS10612,BMG_DS038679,Caudal Duplication Anomaly
+BMGC_DS10613,BMG_DS038681,"Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency"
+BMGC_DS10614,BMG_DS038682,Adult-Onset Vitelliform Macular Dystrophy
+BMGC_DS10615,BMG_DS038684,"Neutropenia, Nonimmune Chronic Idiopathic, Adult"
+BMGC_DS10616,BMG_DS038685,"AURAL ATRESIA, CONGENITAL"
+BMGC_DS10617,BMG_DS038686,"Deafness, Autosomal Dominant 48"
+BMGC_DS10618,BMG_DS038687,"autoimmune disease, susceptibility to, 1"
+BMGC_DS10619,BMG_DS038688,"focal segmental glomerulosclerosis 3, susceptibility to"
+BMGC_DS10620,BMG_DS038689,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K"
+BMGC_DS10621,BMG_DS038690,"Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k"
+BMGC_DS10622,BMG_DS038691,"MITRAL VALVE PROLAPSE, MYXOMATOUS 2"
+BMGC_DS10623,BMG_DS038692,HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME
+BMGC_DS10624,BMG_DS038693,"Alzheimer disease, familial, type 3"
+BMGC_DS10625,BMG_DS038694,"Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques"
+BMGC_DS10626,BMG_DS038695,"Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia"
+BMGC_DS10627,BMG_DS038696,"Deafness, Autosomal Recessive 37"
+BMGC_DS10628,BMG_DS038697,Craniolenticulosutural Dysplasia
+BMGC_DS10629,BMG_DS038698,"Charcot-Marie-Tooth Disease, Dominant Intermediate D"
+BMGC_DS10630,BMG_DS038699,Acrocapitofemoral Dysplasia
+BMGC_DS10631,BMG_DS038700,"Bile acid synthesis defect, congenital, 1"
+BMGC_DS10632,BMG_DS038701,"Hypercholanemia, Familial"
+BMGC_DS10633,BMG_DS038702,"SEIZURES, BENIGN FAMILIAL INFANTILE, 3"
+BMGC_DS10634,BMG_DS038704,"Charcot-Marie-Tooth disease, Type 2J"
+BMGC_DS10635,BMG_DS038705,"Charcot-Marie-Tooth disease, demyelinating, Type 1F"
+BMGC_DS10636,BMG_DS038706,"Charcot-Marie-Tooth disease, Type 2H"
+BMGC_DS10637,BMG_DS038708,Noonan syndrome-like disorder with loose anagen hair
+BMGC_DS10638,BMG_DS038709,"Charcot-Marie-Tooth disease, Type 4A, axonal form"
+BMGC_DS10639,BMG_DS038710,Parkinson Disease 11
+BMGC_DS10640,BMG_DS038711,"Charcot-Marie-Tooth disease, Type 2E"
+BMGC_DS10641,BMG_DS038714,"Charcot-Marie-Tooth disease, Type 1D"
+BMGC_DS10642,BMG_DS038715,IRAK4 Deficiency
+BMGC_DS10643,BMG_DS038716,"Cataract, Congenital, with Mental Impairment and Dentate Gyrus Atrophy"
+BMGC_DS10644,BMG_DS038717,torsion dystonia 13
+BMGC_DS10645,BMG_DS038724,Skin Fragility-Woolly Hair Syndrome
+BMGC_DS10646,BMG_DS038725,"CANDIDIASIS, FAMILIAL CHRONIC NAIL, WITH ICAM1 DEFICIENCY"
+BMGC_DS10647,BMG_DS038726,"Neuronopathy, Distal Hereditary Motor, Type Viib"
+BMGC_DS10648,BMG_DS038727,Van Buchem disease type 2
+BMGC_DS10649,BMG_DS038728,"OSTEOPETROSIS, AUTOSOMAL DOMINANT 1"
+BMGC_DS10650,BMG_DS038729,"ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS"
+BMGC_DS10651,BMG_DS038730,"NIEMANN-PICK DISEASE, TYPE C2"
+BMGC_DS10652,BMG_DS038733,"Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis"
+BMGC_DS10653,BMG_DS038735,Lethal Congenital Contracture Syndrome 2
+BMGC_DS10654,BMG_DS038738,"Pontocerebellar Hypoplasia, Type 1a"
+BMGC_DS10655,BMG_DS038742,"Spastic Paraplegia 24, Autosomal Recessive"
+BMGC_DS10656,BMG_DS038743,"LEPROSY, SUSCEPTIBILITY TO, 2"
+BMGC_DS10657,BMG_DS038744,"spastic paraplegia, ataxia, and intellectual disability"
+BMGC_DS10658,BMG_DS038745,"Atrial fibrillation, familial 1"
+BMGC_DS10659,BMG_DS038749,"Camptosynpolydactyly, complex"
+BMGC_DS10660,BMG_DS038750,"TOENAIL DYSTROPHY, ISOLATED"
+BMGC_DS10661,BMG_DS038751,"migraine with or without aura, susceptibility to, 6"
+BMGC_DS10662,BMG_DS038753,"migraine with or without aura, susceptibility to, 5"
+BMGC_DS10663,BMG_DS038755,"migraine without aura, susceptibility to, 4"
+BMGC_DS10664,BMG_DS038756,"bulimia nervosa, susceptibility to, 1"
+BMGC_DS10665,BMG_DS038757,"migraine with or without aura, susceptibility to, 3"
+BMGC_DS10666,BMG_DS038758,"DYSTONIA 15, MYOCLONIC"
+BMGC_DS10667,BMG_DS038759,"FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED"
+BMGC_DS10668,BMG_DS038760,Biotin-thiamine-responsive basal ganglia disease
+BMGC_DS10669,BMG_DS038761,"CARDIOMYOPATHY, DILATED, 1M"
+BMGC_DS10670,BMG_DS038762,Newfoundland Rod-Cone Dystrophy
+BMGC_DS10671,BMG_DS038763,Bothnia Retinal Dystrophy
+BMGC_DS10672,BMG_DS038764,"VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2"
+BMGC_DS10673,BMG_DS038765,"Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis"
+BMGC_DS10674,BMG_DS038766,SPINOCEREBELLAR ATAXIA WITH EPILEPSY
+BMGC_DS10675,BMG_DS038767,SPINOCEREBELLAR ATAXIA 18
+BMGC_DS10676,BMG_DS038768,GIL BLOOD GROUP
+BMGC_DS10677,BMG_DS038769,SPINOCEREBELLAR ATAXIA 21
+BMGC_DS10678,BMG_DS038770,"Deafness, Autosomal Dominant 44"
+BMGC_DS10679,BMG_DS038771,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 8"
+BMGC_DS10680,BMG_DS038772,coenzyme Q10 deficiency
+BMGC_DS10681,BMG_DS038773,"intellectual disability, autosomal recessive 2"
+BMGC_DS10682,BMG_DS038774,"Hypouricemia, Familial Renal, due to Tubular Hypersecretion"
+BMGC_DS10683,BMG_DS038775,"Hypogonadism, Male, With Mental Retardation And Skeletal Anomalies"
+BMGC_DS10684,BMG_DS038778,"Hydrocephalus, X-Linked, with Congenital Idiopathic Intestinal Pseudoobstruction"
+BMGC_DS10685,BMG_DS038779,Holoprosencephaly with Fetal Akinesia-Hypokinesia Sequence
+BMGC_DS10686,BMG_DS038780,Hirschsprung disease type d brachydactyly
+BMGC_DS10687,BMG_DS038781,Hhhh Syndrome
+BMGC_DS10688,BMG_DS038782,"HETEROTAXY, VISCERAL, 1, X-LINKED"
+BMGC_DS10689,BMG_DS038783,"hernia, anterior diaphragmatic"
+BMGC_DS10690,BMG_DS038784,hemopoietic proliferation
+BMGC_DS10691,BMG_DS038787,"Granulomatous Disease, Chronic, X-Linked"
+BMGC_DS10692,BMG_DS038789,"Granulomas, congenital cerebral"
+BMGC_DS10693,BMG_DS038792,"Membranoproliferative Glomerulonephritis, X-Linked"
+BMGC_DS10694,BMG_DS038793,Fingerprint Body Myopathy
+BMGC_DS10695,BMG_DS038795,"Exudative Vitreoretinopathy, Familial, X-Linked Recessive"
+BMGC_DS10696,BMG_DS038798,X-linked Dyggve-Melchior-Clausen syndrome
+BMGC_DS10697,BMG_DS038799,Dermoids of cornea
+BMGC_DS10698,BMG_DS038801,"Deafness, X-Linked 1"
+BMGC_DS10699,BMG_DS038802,Progressive hearing loss stapes fixation
+BMGC_DS10700,BMG_DS038804,"OTOPALATODIGITAL SYNDROME, TYPE II"
+BMGC_DS10701,BMG_DS038806,"CONE-ROD DYSTROPHY, X-LINKED, 1"
+BMGC_DS10702,BMG_DS038807,"CONE DYSTROPHY, X-LINKED, 1"
+BMGC_DS10703,BMG_DS038808,"CLEFT PALATE, X-LINKED"
+BMGC_DS10704,BMG_DS038809,Cleft Palate with Ankyloglossia
+BMGC_DS10705,BMG_DS038810,Ayazi syndrome
+BMGC_DS10706,BMG_DS038811,Brachytelephalangic Chondrodysplasia Punctata
+BMGC_DS10707,BMG_DS038812,Abruzzo Erickson syndrome
+BMGC_DS10708,BMG_DS038814,Charcot Marie Tooth type 1 aplasia cutis congenita
+BMGC_DS10709,BMG_DS038815,"Charcot-Marie-Tooth disease, X-linked recessive, 3"
+BMGC_DS10710,BMG_DS038816,"Charcot-Marie-Tooth disease, X-linked recessive, 2"
+BMGC_DS10711,BMG_DS038817,"Cerebral Sclerosis, Diffuse, Scholz Type"
+BMGC_DS10712,BMG_DS038818,"SPINOCEREBELLAR ATAXIA, X-LINKED 2"
+BMGC_DS10713,BMG_DS038819,"central incisors, absence of"
+BMGC_DS10714,BMG_DS038820,Catel Manzke syndrome
+BMGC_DS10715,BMG_DS038823,Branchial arch syndrome X-linked
+BMGC_DS10716,BMG_DS038826,"Arthrogryposis multiplex congenita, distal, X-linked"
+BMGC_DS10717,BMG_DS038829,Microphthalmia with ankyloblepharon and intellectual disability syndrome
+BMGC_DS10718,BMG_DS038830,Neural tube defects X-linked
+BMGC_DS10719,BMG_DS038832,"ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA"
+BMGC_DS10720,BMG_DS038833,X-linked reticulate pigmentary disorder
+BMGC_DS10721,BMG_DS038834,"AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2"
+BMGC_DS10722,BMG_DS038835,"AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1"
+BMGC_DS10723,BMG_DS038836,"Amelogenesis Imperfecta, Hypomaturation Type, with Snow-Capped Teeth"
+BMGC_DS10724,BMG_DS038837,Alpha thalassemia X-linked intellectual disability syndrome
+BMGC_DS10725,BMG_DS038838,ALBINISM-DEAFNESS SYNDROME
+BMGC_DS10726,BMG_DS038839,Ocular albinism with late-onset sensorineural deafness
+BMGC_DS10727,BMG_DS038840,"Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked"
+BMGC_DS10728,BMG_DS038841,"Invasive Pneumococcal Disease, Recurrent Isolated, 2"
+BMGC_DS10729,BMG_DS038842,"Lymphoproliferative Syndrome, X-Linked, 2"
+BMGC_DS10730,BMG_DS038843,"Cataracts, ataxia, short stature, and mental retardation"
+BMGC_DS10731,BMG_DS038844,"Deafness, X-Linked 5"
+BMGC_DS10732,BMG_DS038846,Hyperekplexia and Epilepsy
+BMGC_DS10733,BMG_DS038847,Retinitis Pigmentosa 34
+BMGC_DS10734,BMG_DS038848,Premature Ovarian Failure 2b
+BMGC_DS10735,BMG_DS038849,"Nystagmus 5, Infantile Periodic Alternating"
+BMGC_DS10736,BMG_DS038851,SHOX-related short stature
+BMGC_DS10737,BMG_DS038852,Fg Syndrome 5
+BMGC_DS10738,BMG_DS038853,Chromosome Xp11.3 Deletion Syndrome
+BMGC_DS10739,BMG_DS038854,"intellectual disability, X-linked 91"
+BMGC_DS10740,BMG_DS038855,"intellectual disability, X-linked 92"
+BMGC_DS10741,BMG_DS038856,Hartsfield-Bixler-Demyer syndrome
+BMGC_DS10742,BMG_DS038857,"Glycogen Storage Disease, Type IXD"
+BMGC_DS10743,BMG_DS038859,Dent Disease 2
+BMGC_DS10744,BMG_DS038860,"Hypophosphatemic Rickets, X-Linked Recessive"
+BMGC_DS10745,BMG_DS038861,Nephrogenic Syndrome of Inappropriate Antidiuresis
+BMGC_DS10746,BMG_DS038863,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE"
+BMGC_DS10747,BMG_DS038864,Martin-Probst Deafness-Mental Retardation Syndrome
+BMGC_DS10748,BMG_DS038865,"intellectual disability, X-linked 82"
+BMGC_DS10749,BMG_DS038866,"FANCONI ANEMIA, COMPLEMENTATION GROUP B"
+BMGC_DS10750,BMG_DS038867,Premature Ovarian Failure 2a
+BMGC_DS10751,BMG_DS038868,Ovarian Dysgenesis 2
+BMGC_DS10752,BMG_DS038869,Premature Ovarian Failure 4
+BMGC_DS10753,BMG_DS038871,"intellectual disability, X-linked 84"
+BMGC_DS10754,BMG_DS038872,"intellectual disability, X-linked 45"
+BMGC_DS10755,BMG_DS038873,"autism, susceptibility to, X-linked 3"
+BMGC_DS10756,BMG_DS038874,"Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders"
+BMGC_DS10757,BMG_DS038875,"Spinal Muscular Atrophy, Distal, X-Linked 3"
+BMGC_DS10758,BMG_DS038876,"Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance"
+BMGC_DS10759,BMG_DS038878,"CONE-ROD DYSTROPHY, X-LINKED, 3"
+BMGC_DS10760,BMG_DS038879,"Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia"
+BMGC_DS10761,BMG_DS038882,"intellectual disability, X-linked 77"
+BMGC_DS10762,BMG_DS038883,"intellectual disability, X-linked 46"
+BMGC_DS10763,BMG_DS038884,Stocco dos Santos syndrome
+BMGC_DS10764,BMG_DS038885,"intellectual disability, X-linked 81"
+BMGC_DS10765,BMG_DS038886,"autism, susceptibility to, X-linked 2"
+BMGC_DS10766,BMG_DS038887,"autism, susceptibility to, X-linked 1"
+BMGC_DS10767,BMG_DS038888,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HEDERA TYPE"
+BMGC_DS10768,BMG_DS038889,FG syndrome 4
+BMGC_DS10769,BMG_DS038890,FG SYNDROME 3
+BMGC_DS10770,BMG_DS038894,RETINITIS PIGMENTOSA 3
+BMGC_DS10771,BMG_DS038895,Perisylvian syndrome
+BMGC_DS10772,BMG_DS038896,"intellectual disability, X-linked 63"
+BMGC_DS10773,BMG_DS038899,Dyserythropoietic Anemia with Thrombocytopenia
+BMGC_DS10774,BMG_DS038902,"intellectual disability, X-linked 73"
+BMGC_DS10775,BMG_DS038903,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE"
+BMGC_DS10776,BMG_DS038904,"Creatine deficiency, X-linked"
+BMGC_DS10777,BMG_DS038906,"intellectual disability, X-linked 53"
+BMGC_DS10778,BMG_DS038907,"Lesch-Nyhan Syndrome, Neurologic Variant"
+BMGC_DS10779,BMG_DS038908,FG SYNDROME 2
+BMGC_DS10780,BMG_DS038909,"Agammaglobulinemia, X-linked, type 2"
+BMGC_DS10781,BMG_DS038911,"Neutropenia, Severe Congenital, X-Linked"
+BMGC_DS10782,BMG_DS038912,"Ectodermal dysplasia, hypohidrotic, with immune deficiency"
+BMGC_DS10783,BMG_DS038913,ectodermal dysplasia and immunodeficiency 1
+BMGC_DS10784,BMG_DS038914,"Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaly syndrome"
+BMGC_DS10785,BMG_DS038915,URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME
+BMGC_DS10786,BMG_DS038917,"Goiter, Multinodular 2"
+BMGC_DS10787,BMG_DS038919,"intellectual disability, X-linked 72"
+BMGC_DS10788,BMG_DS038921,"Spastic paraplegia 16, X-linked"
+BMGC_DS10789,BMG_DS038922,Siderius X-linked mental retardation syndrome
+BMGC_DS10790,BMG_DS038923,Abidi X-linked mental retardation syndrome
+BMGC_DS10791,BMG_DS038924,Armfield X-Linked Mental Retardation Syndrome
+BMGC_DS10792,BMG_DS038925,Lubs X-linked mental retardation syndrome
+BMGC_DS10793,BMG_DS038926,Roifman syndrome
+BMGC_DS10794,BMG_DS038927,"Ptosis, Hereditary Congenital 2"
+BMGC_DS10795,BMG_DS038928,Terminal Osseous Dysplasia and Pigmentary Defects
+BMGC_DS10796,BMG_DS038929,"Mental retardation X-linked, South African type"
+BMGC_DS10797,BMG_DS038930,HOYERAAL-HREIDARSSON SYNDROME
+BMGC_DS10798,BMG_DS038931,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 11"
+BMGC_DS10799,BMG_DS038933,"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH HYPOMYELINATING LEUKODYSTROPHY"
+BMGC_DS10800,BMG_DS038934,testicular germ cell tumor 1
+BMGC_DS10801,BMG_DS038936,Myotubular Myopathy with Abnormal Genital Development
+BMGC_DS10802,BMG_DS038937,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 7"
+BMGC_DS10803,BMG_DS038938,"Lissencephaly, X-Linked, 2"
+BMGC_DS10804,BMG_DS038939,Hydranencephaly and Abnormal Genitalia
+BMGC_DS10805,BMG_DS038940,"EPISODIC MUSCLE WEAKNESS, X-LINKED"
+BMGC_DS10806,BMG_DS038941,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 58"
+BMGC_DS10807,BMG_DS038942,Simpson Golabi Behmel syndrome type 2
+BMGC_DS10808,BMG_DS038944,"Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis"
+BMGC_DS10809,BMG_DS038947,"Microphthalmia, syndromic 2"
+BMGC_DS10810,BMG_DS038948,"ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED"
+BMGC_DS10811,BMG_DS038949,MEHMO syndrome
+BMGC_DS10812,BMG_DS038950,"prostate cancer, hereditary, X-linked 1"
+BMGC_DS10813,BMG_DS038952,Juvenile-onset dystonia
+BMGC_DS10814,BMG_DS038953,"Bartter syndrome, type 3"
+BMGC_DS10815,BMG_DS038954,"Bartter Syndrome, Type 3, with Hypocalciuria"
+BMGC_DS10816,BMG_DS038955,Meckel syndrome type 3
+BMGC_DS10817,BMG_DS038957,Spinocerebellar ataxia 19
+BMGC_DS10818,BMG_DS038958,isolated focal cortical dysplasia type II
+BMGC_DS10819,BMG_DS038959,"Focal Cortical Dysplasia of Taylor, Type IIa"
+BMGC_DS10820,BMG_DS038960,"CORTICAL DYSPLASIA OF TAYLOR, DYSPLASIA ONLY"
+BMGC_DS10821,BMG_DS038961,"Focal Cortical Dysplasia of Taylor, Type IIb"
+BMGC_DS10822,BMG_DS038962,"CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 1"
+BMGC_DS10823,BMG_DS038963,Lathosterolosis
+BMGC_DS10824,BMG_DS038965,Smith-McCort dysplasia
+BMGC_DS10825,BMG_DS038966,odontoid hypoplasia
+BMGC_DS10826,BMG_DS038968,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4"
+BMGC_DS10827,BMG_DS038969,Horizontal gaze palsy with progressive scoliosis
+BMGC_DS10828,BMG_DS038970,cataract 27
+BMGC_DS10829,BMG_DS038971,CONE-ROD DYSTROPHY 10
+BMGC_DS10830,BMG_DS038973,"ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1"
+BMGC_DS10831,BMG_DS038974,Autoimmune Lymphoproliferative Syndrome Type 2B
+BMGC_DS10832,BMG_DS038975,"SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE"
+BMGC_DS10833,BMG_DS038978,"DEAFNESS, AUTOSOMAL RECESSIVE 33"
+BMGC_DS10834,BMG_DS038979,"Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration"
+BMGC_DS10835,BMG_DS038983,Thyroid Dyshormonogenesis 6
+BMGC_DS10836,BMG_DS038984,"Deafness, Autosomal Recessive"
+BMGC_DS10837,BMG_DS038985,Amish lethal microcephaly
+BMGC_DS10838,BMG_DS038987,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I"
+BMGC_DS10839,BMG_DS038988,"Spastic paraplegia 19, autosomal dominant"
+BMGC_DS10840,BMG_DS038989,MOYAMOYA DISEASE 2
+BMGC_DS10841,BMG_DS038990,SPINOCEREBELLAR ATAXIA 17
+BMGC_DS10842,BMG_DS038991,SPECIFIC LANGUAGE IMPAIRMENT 3
+BMGC_DS10843,BMG_DS038993,Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies
+BMGC_DS10844,BMG_DS038995,"nasopharyngeal carcinoma, susceptibility to, 1"
+BMGC_DS10845,BMG_DS038996,"Deafness, Autosomal Recessive 30"
+BMGC_DS10846,BMG_DS038997,Joubert syndrome 4
+BMGC_DS10847,BMG_DS038998,Anauxetic dysplasia
+BMGC_DS10848,BMG_DS039000,"Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3"
+BMGC_DS10849,BMG_DS039001,"Aortic Aneurysm, Familial Thoracic 2"
+BMGC_DS10850,BMG_DS039003,"DEAFNESS, AUTOSOMAL RECESSIVE 31"
+BMGC_DS10851,BMG_DS039004,"EPIPHYSEAL DYSPLASIA, MULTIPLE, 5"
+BMGC_DS10852,BMG_DS039006,"PARKINSON DISEASE 8, AUTOSOMAL DOMINANT"
+BMGC_DS10853,BMG_DS039007,"Deafness, Autosomal Recessive 22"
+BMGC_DS10854,BMG_DS039008,"Deafness, Autosomal Dominant 21"
+BMGC_DS10855,BMG_DS039009,"Brachydactyly, Type A1, B"
+BMGC_DS10856,BMG_DS039010,SENIOR-LOKEN SYNDROME 4
+BMGC_DS10857,BMG_DS039011,Senior-Loken Syndrome 3
+BMGC_DS10858,BMG_DS039012,"Hyperreninemic Hypoaldosteronism, Familial, 2"
+BMGC_DS10859,BMG_DS039014,NEPHRONOPHTHISIS 4
+BMGC_DS10860,BMG_DS039015,"PULMONARY DISEASE, CHRONIC OBSTRUCTIVE, SEVERE EARLY-ONSET"
+BMGC_DS10861,BMG_DS039016,Oculocutaneous albinism type 1B
+BMGC_DS10862,BMG_DS039017,"USHER SYNDROME, TYPE IG"
+BMGC_DS10863,BMG_DS039018,"ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE"
+BMGC_DS10864,BMG_DS039020,"Symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch"
+BMGC_DS10865,BMG_DS039022,"Vascular Malformation, Primary Intraosseous"
+BMGC_DS10866,BMG_DS039023,ALZHEIMER DISEASE 4
+BMGC_DS10867,BMG_DS039024,Paraganglioma and gastric stromal sarcoma syndrome
+BMGC_DS10868,BMG_DS039025,"pancreatic cancer, susceptibility to, 1"
+BMGC_DS10869,BMG_DS039026,"POLYMICROGYRIA, BILATERAL FRONTOPARIETAL"
+BMGC_DS10870,BMG_DS039028,Cree Mental Retardation Syndrome
+BMGC_DS10871,BMG_DS039029,Cardioneuromyopathy with Hyaline Masses and Nemaline Rods
+BMGC_DS10872,BMG_DS039030,"Faciomandibular myoclonus, nocturnal"
+BMGC_DS10873,BMG_DS039031,"Digital Arthropathy-Brachydactyly, Familial"
+BMGC_DS10874,BMG_DS039032,FRIEDREICH ATAXIA WITH RETAINED REFLEXES
+BMGC_DS10875,BMG_DS039034,"anorexia nervosa, susceptibility to, 1"
+BMGC_DS10876,BMG_DS039035,Peripheral Arterial Occlusive Disease 1
+BMGC_DS10877,BMG_DS039036,Glut1 Deficiency Syndrome
+BMGC_DS10878,BMG_DS039037,hemifacial myohyperplasia
+BMGC_DS10879,BMG_DS039038,MOMES Syndrome
+BMGC_DS10880,BMG_DS039039,Hyperopic Astigmatism
+BMGC_DS10881,BMG_DS039040,"MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET"
+BMGC_DS10882,BMG_DS039041,"Azoospermia, Nonobstructive"
+BMGC_DS10883,BMG_DS039042,"Primary ciliary dyskinesia, 2"
+BMGC_DS10884,BMG_DS039043,"Hyperinsulinemic hypoglycemia, familial, 6"
+BMGC_DS10885,BMG_DS039044,SECKEL SYNDROME 2
+BMGC_DS10886,BMG_DS039046,"EPIPHYSEAL DYSPLASIA, MULTIPLE, 4"
+BMGC_DS10887,BMG_DS039047,Van der Woude syndrome 2
+BMGC_DS10888,BMG_DS039048,SPECIFIC LANGUAGE IMPAIRMENT 2
+BMGC_DS10889,BMG_DS039049,SPECIFIC LANGUAGE IMPAIRMENT 1
+BMGC_DS10890,BMG_DS039051,"Deafness, Autosomal Dominant 36"
+BMGC_DS10891,BMG_DS039052,"Dyskinesia, Familial, with Facial Myokymia"
+BMGC_DS10892,BMG_DS039053,KUFOR-RAKEB SYNDROME
+BMGC_DS10893,BMG_DS039055,SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES
+BMGC_DS10894,BMG_DS039056,"CARDIOMYOPATHY, DILATED, 1L"
+BMGC_DS10895,BMG_DS039059,"nonarteritic anterior ischemic optic neuropathy, susceptibility to"
+BMGC_DS10896,BMG_DS039061,Hypermethioninemia due to deficiency of glycine N-methyltransferase
+BMGC_DS10897,BMG_DS039063,"melanoma, uveal, susceptibility to, 2"
+BMGC_DS10898,BMG_DS039064,"melanoma, uveal, susceptibility to, 1"
+BMGC_DS10899,BMG_DS039065,SPINOCEREBELLAR ATAXIA 15
+BMGC_DS10900,BMG_DS039066,"glaucoma, normal tension, susceptibility to"
+BMGC_DS10901,BMG_DS039068,Amyotrophic Lateral Sclerosis 3
+BMGC_DS10902,BMG_DS039070,"MUSCULAR DYSTROPHY, CONGENITAL, 1C"
+BMGC_DS10903,BMG_DS039071,Waardenburg Syndrome Type 1
+BMGC_DS10904,BMG_DS039072,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F"
+BMGC_DS10905,BMG_DS039073,LIG4 Syndrome
+BMGC_DS10906,BMG_DS039074,"polysubstance abuse, susceptibility to"
+BMGC_DS10907,BMG_DS039075,vitiligo-associated multiple autoimmune disease susceptibility 1
+BMGC_DS10908,BMG_DS039076,"Oculocutaneous Albinism, Type IV"
+BMGC_DS10909,BMG_DS039077,"Episodic Ataxia, Type 3"
+BMGC_DS10910,BMG_DS039078,"EPISODIC ATAXIA, TYPE 4"
+BMGC_DS10911,BMG_DS039080,Homozygous 11p15-p14 Deletion Syndrome
+BMGC_DS10912,BMG_DS039082,PHACE association
+BMGC_DS10913,BMG_DS039083,"Charcot-Marie-Tooth Disease, Dominant Intermediate A"
+BMGC_DS10914,BMG_DS039084,"Charcot-Marie-Tooth Disease, Dominant Intermediate B"
+BMGC_DS10915,BMG_DS039085,"Charcot-Marie-Tooth Neuropathy, Dominant Intermediate B, with Neutropenia"
+BMGC_DS10916,BMG_DS039086,Ovarioleukodystrophy
+BMGC_DS10917,BMG_DS039087,"Deafness, Autosomal Dominant 30"
+BMGC_DS10918,BMG_DS039088,Persistent Polyclonal B-Cell Lymphocytosis
+BMGC_DS10919,BMG_DS039089,HUNTINGTON DISEASE-LIKE 2
+BMGC_DS10920,BMG_DS039090,Ehlers-Danlos syndrome caused by tenascin-X deficiency
+BMGC_DS10921,BMG_DS039091,Hypotonia-Cystinuria Syndrome
+BMGC_DS10922,BMG_DS039093,"migraine, familial typical, susceptibility to, 2"
+BMGC_DS10923,BMG_DS039094,"Mental Retardation, X-Linked, with Isolated Growth Hormone Deficiency"
+BMGC_DS10924,BMG_DS039095,Lissencephaly and agenesis of corpus callosum
+BMGC_DS10925,BMG_DS039096,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 50"
+BMGC_DS10926,BMG_DS039097,"Spondyloepimetaphyseal Dysplasia, X-Linked"
+BMGC_DS10927,BMG_DS039098,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 9
+BMGC_DS10928,BMG_DS039099,"X Inactivation, Familial Skewed, 1"
+BMGC_DS10929,BMG_DS039100,"CONE-ROD DYSTROPHY, X-LINKED, 2"
+BMGC_DS10930,BMG_DS039101,"COGNITIVE FUNCTION 1, SOCIAL"
+BMGC_DS10931,BMG_DS039102,Woods Black Norbury syndrome
+BMGC_DS10932,BMG_DS039103,"Fetal akinesia syndrome, X-linked"
+BMGC_DS10933,BMG_DS039104,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A"
+BMGC_DS10934,BMG_DS039106,X-Linked Lissencephaly
+BMGC_DS10935,BMG_DS039107,"SUBCORTICAL BAND HETEROTOPIA, X-LINKED"
+BMGC_DS10936,BMG_DS039108,Subcortical Band Heterotopia
+BMGC_DS10937,BMG_DS039109,"Deafness, X-Linked 4"
+BMGC_DS10938,BMG_DS039111,"Periventricular Heterotopia, X-Linked"
+BMGC_DS10939,BMG_DS039113,DOSAGE-SENSITIVE SEX REVERSAL
+BMGC_DS10940,BMG_DS039114,Dent disease 1
+BMGC_DS10941,BMG_DS039116,Zunich neuroectodermal syndrome
+BMGC_DS10942,BMG_DS039118,"Xeroderma pigmentosum, variant type"
+BMGC_DS10943,BMG_DS039119,"XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E"
+BMGC_DS10944,BMG_DS039122,"WOOLLY HAIR, AUTOSOMAL RECESSIVE 1, WITH OR WITHOUT HYPOTRICHOSIS"
+BMGC_DS10945,BMG_DS039123,Mental retardation Wolff type
+BMGC_DS10946,BMG_DS039125,WHITE FORELOCK WITH MALFORMATIONS
+BMGC_DS10947,BMG_DS039126,"Whistling face syndrome, recessive form"
+BMGC_DS10948,BMG_DS039128,Pierre Robin syndrome with fetal chondrodysplasia
+BMGC_DS10949,BMG_DS039129,"WAARDENBURG SYNDROME, TYPE 4A"
+BMGC_DS10950,BMG_DS039131,Pontocerebellar Hypoplasia Type 2A
+BMGC_DS10951,BMG_DS039134,Ataxia with vitamin E deficiency
+BMGC_DS10952,BMG_DS039135,"VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1"
+BMGC_DS10953,BMG_DS039136,"Methylmalonic Aciduria and Homocystinuria, CblD Type"
+BMGC_DS10954,BMG_DS039137,"Homocystinuria, CblD Type, Variant 1"
+BMGC_DS10955,BMG_DS039138,"Methylmalonic Aciduria, CblD Type, Variant 2"
+BMGC_DS10956,BMG_DS039139,Cobalamin C disease
+BMGC_DS10957,BMG_DS039140,"Methylmalonic Aciduria and Homocystinuria, CblF Type"
+BMGC_DS10958,BMG_DS039141,Visceral myopathy familial external ophthalmoplegia
+BMGC_DS10959,BMG_DS039142,Isolated hypoplasia of the right ventricle
+BMGC_DS10960,BMG_DS039143,Vascular Hyalinosis
+BMGC_DS10961,BMG_DS039144,Van Bogaert-Hozay syndrome
+BMGC_DS10962,BMG_DS039145,VACTERL Association With Hydrocephalus
+BMGC_DS10963,BMG_DS039147,"USHER SYNDROME, TYPE IC"
+BMGC_DS10964,BMG_DS039148,"USHER SYNDROME, TYPE IIA"
+BMGC_DS10965,BMG_DS039151,Ulnar Agenesis and Endocardial Fibroelastosis
+BMGC_DS10966,BMG_DS039152,Ulnar Hypoplasia with Mental Retardation
+BMGC_DS10967,BMG_DS039153,Al Awadi syndrome
+BMGC_DS10968,BMG_DS039156,T-substance anomaly
+BMGC_DS10969,BMG_DS039157,Distal amyotrophy
+BMGC_DS10970,BMG_DS039159,Oliver-McFarlane syndrome
+BMGC_DS10971,BMG_DS039160,"Tricarboxylic Acid Cycle, Defect of"
+BMGC_DS10972,BMG_DS039161,"TONGUE, PIGMENTED FUNGIFORM PAPILLAE OF"
+BMGC_DS10973,BMG_DS039164,"Graves disease, susceptibility to, 1"
+BMGC_DS10974,BMG_DS039165,Thyroid Dyshormonogenesis 1
+BMGC_DS10975,BMG_DS039166,Thymic-Renal-Anal-Lung dysplasia
+BMGC_DS10976,BMG_DS039167,Thyrocerebral-retinal syndrome
+BMGC_DS10977,BMG_DS039168,"thymoma, familial"
+BMGC_DS10978,BMG_DS039170,"Thumb, Hypoplastic, with Choroid Coloboma, Poorly Developed Antihelix, and Deafness"
+BMGC_DS10979,BMG_DS039171,"thumb, distal hyperextensibility of"
+BMGC_DS10980,BMG_DS039172,"Thumb Agenesis, Short Stature, And Immunodeficiency"
+BMGC_DS10981,BMG_DS039174,inherited threoninemia
+BMGC_DS10982,BMG_DS039175,Miller-McKusick-Malvaux-Syndrome (3M Syndrome)
+BMGC_DS10983,BMG_DS039176,Thoracomelic Dysplasia
+BMGC_DS10984,BMG_DS039178,Thanatophoric dysplasia Glasgow variant
+BMGC_DS10985,BMG_DS039179,"testes, rudimentary"
+BMGC_DS10986,BMG_DS039180,"teratoma, pineal"
+BMGC_DS10987,BMG_DS039183,Teebi Shaltout syndrome
+BMGC_DS10988,BMG_DS039184,"Tay-Sachs Disease, Juvenile"
+BMGC_DS10989,BMG_DS039185,"Hexosaminidase A Deficiency, Adult Type"
+BMGC_DS10990,BMG_DS039187,"Tay-Sachs Disease, Variant B1"
+BMGC_DS10991,BMG_DS039189,Hexosaminidase alpha-Subunit Deficiency (Variant B)
+BMGC_DS10992,BMG_DS039190,Tatsumi Factor Deficiency
+BMGC_DS10993,BMG_DS039192,SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME
+BMGC_DS10994,BMG_DS039193,Cold-induced sweating syndrome 1
+BMGC_DS10995,BMG_DS039194,generalized dystonia
+BMGC_DS10996,BMG_DS039195,"Sucrosuria, Hiatus Hernia and Mental Retardation"
+BMGC_DS10997,BMG_DS039197,"SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE"
+BMGC_DS10998,BMG_DS039198,"Spondyloepiphyseal dysplasia tarda, Toledo type"
+BMGC_DS10999,BMG_DS039199,Spondyloepiphyseal Dysplasia Tarda with Mental Retardation
+BMGC_DS11000,BMG_DS039200,"Spondyloepiphyseal Dysplasia Tarda, Autosomal Recessive"
+BMGC_DS11001,BMG_DS039201,"Brachyolmia, recessive Hobaek type"
+BMGC_DS11002,BMG_DS039202,Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies
+BMGC_DS11003,BMG_DS039203,Mousa Al din Al Nassar syndrome
+BMGC_DS11004,BMG_DS039204,Corneal cerebellar syndrome
+BMGC_DS11005,BMG_DS039206,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 3"
+BMGC_DS11006,BMG_DS039207,Infantile onset spinocerebellar ataxia
+BMGC_DS11007,BMG_DS039209,"Spinal muscular atrophy, Ryukyuan type"
+BMGC_DS11008,BMG_DS039211,Spinal Muscular Atrophy with Mental Retardation
+BMGC_DS11009,BMG_DS039212,"Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation"
+BMGC_DS11010,BMG_DS039213,"Spastic Paresis, Glaucoma, and Mental Retardation"
+BMGC_DS11011,BMG_DS039215,"Spastic Paraplegia 5a, Autosomal Recessive"
+BMGC_DS11012,BMG_DS039216,"Spastic paraplegia 15, autosomal recessive"
+BMGC_DS11013,BMG_DS039217,Spastic diplegia infantile type
+BMGC_DS11014,BMG_DS039218,"SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE"
+BMGC_DS11015,BMG_DS039219,Spastic Ataxia
+BMGC_DS11016,BMG_DS039220,"Insulin-Like Growth Factor I, Resistance To"
+BMGC_DS11017,BMG_DS039222,sodium-potassium-ATPase activity of red cell
+BMGC_DS11018,BMG_DS039223,peeling skin syndrome 1
+BMGC_DS11019,BMG_DS039226,"Severe combined immunodeficiency, atypical"
+BMGC_DS11020,BMG_DS039229,Second Metatarsal-Metacarpal Syndrome
+BMGC_DS11021,BMG_DS039230,Rodrigues blindness
+BMGC_DS11022,BMG_DS039231,"Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction"
+BMGC_DS11023,BMG_DS039232,"Robinow syndrome, autosomal recessive"
+BMGC_DS11024,BMG_DS039233,Richieri Costa Pereira syndrome
+BMGC_DS11025,BMG_DS039234,Rhizomelic syndrome
+BMGC_DS11026,BMG_DS039235,"Myoglobinuria, Acute Recurrent, Autosomal Recessive"
+BMGC_DS11027,BMG_DS039236,"Rh-Null, Regulator Type"
+BMGC_DS11028,BMG_DS039237,Enhanced S-Cone Syndrome
+BMGC_DS11029,BMG_DS039239,"Retinopathy, Pericentral Pigmentary, Autosomal Recessive"
+BMGC_DS11030,BMG_DS039241,"Retinitis Pigmentosa, Late-Adult Onset"
+BMGC_DS11031,BMG_DS039242,"Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism"
+BMGC_DS11032,BMG_DS039245,Knobloch syndrome
+BMGC_DS11033,BMG_DS039246,Retinal Degeneration and Epilepsy
+BMGC_DS11034,BMG_DS039248,"Renal, Genital, and Middle Ear Anomalies"
+BMGC_DS11035,BMG_DS039249,"Renal tubular acidosis, distal, type 3"
+BMGC_DS11036,BMG_DS039250,Mainzer-Saldino Disease
+BMGC_DS11037,BMG_DS039253,Reese Retinal Dysplasia
+BMGC_DS11038,BMG_DS039254,Red skin pigment anomaly of New Guinea
+BMGC_DS11039,BMG_DS039255,Rapadilino syndrome
+BMGC_DS11040,BMG_DS039256,"Radioulnar Synostosis, Unilateral, with Developmental Retardation and Hypotonia"
+BMGC_DS11041,BMG_DS039257,"Radiculoneuropathy, Fatal Neonatal"
+BMGC_DS11042,BMG_DS039258,"Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to"
+BMGC_DS11043,BMG_DS039259,"EPILEPSY, PYRIDOXINE-DEPENDENT"
+BMGC_DS11044,BMG_DS039260,Pyknoachondrogenesis
+BMGC_DS11045,BMG_DS039262,congenital pulmonary lymphangiectasia
+BMGC_DS11046,BMG_DS039263,Pulmonary Bullae Causing Pneumothorax
+BMGC_DS11047,BMG_DS039264,Pseudouridinuria and Mental Defect
+BMGC_DS11048,BMG_DS039265,Pseudotrisomy 13 syndrome
+BMGC_DS11049,BMG_DS039268,Peroxisomal ACYL-COA oxidase deficiency
+BMGC_DS11050,BMG_DS039269,"Fundus dystrophy, pseudoinflammatory recessive form"
+BMGC_DS11051,BMG_DS039271,"Pseudohermaphroditism, Female, with Skeletal Anomalies"
+BMGC_DS11052,BMG_DS039272,Prolactin Deficiency with Obesity and Enlarged Testes
+BMGC_DS11053,BMG_DS039273,Progesterone Resistance
+BMGC_DS11054,BMG_DS039274,Hyperphenylalaninemia with primapterinuria
+BMGC_DS11055,BMG_DS039275,prenatal bowing
+BMGC_DS11056,BMG_DS039276,"POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE"
+BMGC_DS11057,BMG_DS039277,Bonneau Syndrome
+BMGC_DS11058,BMG_DS039278,"Polyhydramnios, Chronic Idiopathic"
+BMGC_DS11059,BMG_DS039279,"polysaccharide, storage of unusual"
+BMGC_DS11060,BMG_DS039280,"Polyglucosan Body Disease, Adult Form"
+BMGC_DS11061,BMG_DS039281,Infantile polymyoclonus
+BMGC_DS11062,BMG_DS039283,"Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia"
+BMGC_DS11063,BMG_DS039284,Periportal fibrosis
+BMGC_DS11064,BMG_DS039287,Platelet Prostacyclin Receptor Defect
+BMGC_DS11065,BMG_DS039289,Kowarski syndrome
+BMGC_DS11066,BMG_DS039290,Achromatopsia 3
+BMGC_DS11067,BMG_DS039292,Pili torti developmental delay neurological abnormalities
+BMGC_DS11068,BMG_DS039293,"Glycogen Storage Disease of Heart, Lethal Congenital"
+BMGC_DS11069,BMG_DS039294,"Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial"
+BMGC_DS11070,BMG_DS039295,phenformin 4-hydroxylation
+BMGC_DS11071,BMG_DS039298,persistent Mullerian duct syndrome
+BMGC_DS11072,BMG_DS039299,Presentey Anomaly
+BMGC_DS11073,BMG_DS039300,"peroneus tertius muscle, absence of"
+BMGC_DS11074,BMG_DS039301,"Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain"
+BMGC_DS11075,BMG_DS039303,Pelviscapular dysplasia
+BMGC_DS11076,BMG_DS039305,"Pelizaeus-Merzbacher-like disease, autosomal recessive, 2"
+BMGC_DS11077,BMG_DS039306,Pelger-Huet-Like Anomaly and Episodic Fever with Abdominal Pain
+BMGC_DS11078,BMG_DS039307,PEHO syndrome
+BMGC_DS11079,BMG_DS039308,"Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome"
+BMGC_DS11080,BMG_DS039310,"Supranuclear Palsy, Progressive, 1, Atypical"
+BMGC_DS11081,BMG_DS039311,Parana Hard Skin Syndrome
+BMGC_DS11082,BMG_DS039314,"Pancreatic Agenesis, Congenital"
+BMGC_DS11083,BMG_DS039315,Pallidopyramidal syndrome
+BMGC_DS11084,BMG_DS039319,PA polymorphism of alpha-2-globulin
+BMGC_DS11085,BMG_DS039320,Otoonychoperoneal Syndrome
+BMGC_DS11086,BMG_DS039321,RAINE SYNDROME
+BMGC_DS11087,BMG_DS039322,"Osteopetrosis, mild autosomal recessive form"
+BMGC_DS11088,BMG_DS039323,"Osteopetrosis, Autosomal Recessive 1"
+BMGC_DS11089,BMG_DS039324,Kaler Garrity Stern syndrome
+BMGC_DS11090,BMG_DS039325,osteoma of middle ear
+BMGC_DS11091,BMG_DS039327,multicentric osteolysis-nodulosis-arthropathy spectrum
+BMGC_DS11092,BMG_DS039328,Bruck syndrome 1
+BMGC_DS11093,BMG_DS039329,"Osteogenesis Imperfecta, Type IX"
+BMGC_DS11094,BMG_DS039330,"Osteogenesis imperfecta congenita, microcephaly, and cataracts"
+BMGC_DS11095,BMG_DS039331,"Osteodysplasty, Precocious, Of Danks, Mayne, And Kozlowski"
+BMGC_DS11096,BMG_DS039334,"oral sensibility, disturbance of"
+BMGC_DS11097,BMG_DS039335,Optic atrophy 6
+BMGC_DS11098,BMG_DS039336,Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria
+BMGC_DS11099,BMG_DS039337,autosomal recessive progressive external ophthalmoplegia
+BMGC_DS11100,BMG_DS039338,Ophthalmoplegia Totalis with Ptosis and Miosis
+BMGC_DS11101,BMG_DS039339,Onychotrichodysplasia and neutropenia
+BMGC_DS11102,BMG_DS039340,Omphalocele cleft palate syndrome lethal
+BMGC_DS11103,BMG_DS039341,Omodysplasia type 1
+BMGC_DS11104,BMG_DS039343,Oliver Syndrome
+BMGC_DS11105,BMG_DS039344,exstrophy-epispadias complex
+BMGC_DS11106,BMG_DS039345,Oculorenocerebellar syndrome
+BMGC_DS11107,BMG_DS039347,Oculopalatocerebral Syndrome
+BMGC_DS11108,BMG_DS039349,Mosaic variegated aneuploidy syndrome 1
+BMGC_DS11109,BMG_DS039350,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B"
+BMGC_DS11110,BMG_DS039352,NEUTROPHIL ACTIN DYSFUNCTION
+BMGC_DS11111,BMG_DS039353,"Neutropenia, Lethal Congenital, with Eosinophilia"
+BMGC_DS11112,BMG_DS039355,"Neuropathy, Painful"
+BMGC_DS11113,BMG_DS039358,GIANT AXONAL NEUROPATHY 1
+BMGC_DS11114,BMG_DS039360,"Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive"
+BMGC_DS11115,BMG_DS039361,NAVAJO NEUROHEPATOPATHY
+BMGC_DS11116,BMG_DS039362,Navajo Familial Neurogenic Arthropathy
+BMGC_DS11117,BMG_DS039363,"CEROID LIPOFUSCINOSIS, NEURONAL, 5"
+BMGC_DS11118,BMG_DS039364,"CEROID LIPOFUSCINOSIS, NEURONAL, 1"
+BMGC_DS11119,BMG_DS039367,Nephrosis deafness urinary tract digital malformation
+BMGC_DS11120,BMG_DS039369,Atelosteogenesis type 2
+BMGC_DS11121,BMG_DS039370,De La Chapelle Dysplasia
+BMGC_DS11122,BMG_DS039371,Nakajo syndrome
+BMGC_DS11123,BMG_DS039372,Nemaline Myopathy 2
+BMGC_DS11124,BMG_DS039375,Leigh Syndrome due to Mitochondrial Complex IV Deficiency
+BMGC_DS11125,BMG_DS039377,Native American myopathy
+BMGC_DS11126,BMG_DS039378,Nathalie syndrome
+BMGC_DS11127,BMG_DS039379,Nasodigitoacoustic syndrome
+BMGC_DS11128,BMG_DS039381,"Myosclerosis, Autosomal Recessive"
+BMGC_DS11129,BMG_DS039382,Minicore Myopathy with External Ophthalmoplegia
+BMGC_DS11130,BMG_DS039383,"Myopathy, Hyaline Body, Autosomal Recessive"
+BMGC_DS11131,BMG_DS039385,"MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE"
+BMGC_DS11132,BMG_DS039387,"Myopathy, Granulovacuolar Lobular, with Electrical Myotonia"
+BMGC_DS11133,BMG_DS039388,"Myopathy, congenital nonprogressive with Moebius and Robin sequences"
+BMGC_DS11134,BMG_DS039391,myoclonic epilepsy of Lafora 2
+BMGC_DS11135,BMG_DS039392,"myoclonic epilepsy, juvenile, susceptibility to, 1"
+BMGC_DS11136,BMG_DS039393,"Myeloproliferative Disease, Autosomal Recessive"
+BMGC_DS11137,BMG_DS039394,Congenital myasthenic syndrome ib
+BMGC_DS11138,BMG_DS039395,"Myasthenia, Congenital, Refractory to Acetylcholinesterase Inhibitors"
+BMGC_DS11139,BMG_DS039396,"Musk, Inability to Smell"
+BMGC_DS11140,BMG_DS039397,"Muscular Hypertonia, Lethal"
+BMGC_DS11141,BMG_DS039398,"Muscular Dystrophy, Congenital, with Rapid Progression"
+BMGC_DS11142,BMG_DS039399,"Muscular dystrophy, congenital, infantile with cataract and hypogonadism"
+BMGC_DS11143,BMG_DS039401,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B"
+BMGC_DS11144,BMG_DS039402,Gastrocutaneous syndrome
+BMGC_DS11145,BMG_DS039405,"Gamma-A-Globulin, Defect in Assembly of"
+BMGC_DS11146,BMG_DS039406,"FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, OF SORSBY"
+BMGC_DS11147,BMG_DS039408,"Corneal dystrophy, Fuchs' endothelial, 1"
+BMGC_DS11148,BMG_DS039412,"Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness"
+BMGC_DS11149,BMG_DS039417,"fourth cranial nerve palsy, familial congenital"
+BMGC_DS11150,BMG_DS039421,"FINGER LOCKING, RECURRENT, WITH INTRAUTERINE GROWTH RETARDATION AND PROPORTIONATE SHORT STATURE"
+BMGC_DS11151,BMG_DS039423,LAURIN-SANDROW SYNDROME
+BMGC_DS11152,BMG_DS039424,"Laurin-Sandrow Syndrome, Segmental"
+BMGC_DS11153,BMG_DS039425,"Fibrosis Of Extraocular Muscles, Congenital, 1"
+BMGC_DS11154,BMG_DS039426,Jones syndrome
+BMGC_DS11155,BMG_DS039427,"Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia"
+BMGC_DS11156,BMG_DS039428,"Desmoid disease, hereditary"
+BMGC_DS11157,BMG_DS039429,SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS
+BMGC_DS11158,BMG_DS039430,Fibrinolytic Defect
+BMGC_DS11159,BMG_DS039432,Ectopia lentis isolated
+BMGC_DS11160,BMG_DS039433,"Iron Overload, Autosomal Dominant"
+BMGC_DS11161,BMG_DS039434,"Familial Mediterranean Fever, Autosomal Dominant"
+BMGC_DS11162,BMG_DS039435,Familial Multiple Coagulation Factor Deficiency VI
+BMGC_DS11163,BMG_DS039437,Familial Multiple Coagulation Factor Deficiency II
+BMGC_DS11164,BMG_DS039438,Familial Multiple Coagulation Factor Deficiency IV
+BMGC_DS11165,BMG_DS039439,Factor V Excess with Spontaneous Thrombosis
+BMGC_DS11166,BMG_DS039440,"Facial Palsy, Familial Recurrent Peripheral"
+BMGC_DS11167,BMG_DS039441,Exudative vitreoretinopathy 1
+BMGC_DS11168,BMG_DS039443,"EXOSTOSES, MULTIPLE, TYPE II"
+BMGC_DS11169,BMG_DS039444,"Exostoses with Anetodermia and Brachydactyly, Type E"
+BMGC_DS11170,BMG_DS039445,Cerebrooculofacioskeletal Syndrome 3
+BMGC_DS11171,BMG_DS039446,"Exchondrosis Of Pinna, Posterior"
+BMGC_DS11172,BMG_DS039448,Greither Disease
+BMGC_DS11173,BMG_DS039449,Erythrokeratodermia with ataxia
+BMGC_DS11174,BMG_DS039450,Erythema Palmare Hereditarium
+BMGC_DS11175,BMG_DS039451,"Erythema nodosum, familial"
+BMGC_DS11176,BMG_DS039452,"Aortic aneurysm, familial thoracic 4"
+BMGC_DS11177,BMG_DS039455,familial cylindromatosis
+BMGC_DS11178,BMG_DS039456,"Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness"
+BMGC_DS11179,BMG_DS039459,Benign Occipital Epilepsy
+BMGC_DS11180,BMG_DS039460,Epidermolysis Bullosa with Deficiency of Galactosylhydroxylysyl Glucosyltransferase
+BMGC_DS11181,BMG_DS039461,Transient bullous dermolysis of the newborn
+BMGC_DS11182,BMG_DS039464,"MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA"
+BMGC_DS11183,BMG_DS039465,EOSINOPHILOPENIA
+BMGC_DS11184,BMG_DS039466,"endometriosis, susceptibility to, 1"
+BMGC_DS11185,BMG_DS039468,LATERAL MENINGOCELE SYNDROME
+BMGC_DS11186,BMG_DS039469,"Emphysema, Hereditary Pulmonary"
+BMGC_DS11187,BMG_DS039470,Elliptocytosis 2
+BMGC_DS11188,BMG_DS039471,electroencephalographic peculiarity: fronto-precentral beta wave groups
+BMGC_DS11189,BMG_DS039472,electroencephalographic peculiarity: 14 and 6 per sec. positive spike phenomenon
+BMGC_DS11190,BMG_DS039473,EDS VIIB
+BMGC_DS11191,BMG_DS039474,"ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1"
+BMGC_DS11192,BMG_DS039475,"Edema, Familial Idiopathic, Prepubertal"
+BMGC_DS11193,BMG_DS039477,Ectrodactyly and Ectodermal Dysplasia without Cleft Lip-Palate
+BMGC_DS11194,BMG_DS039478,Ectodermal dysplasia adrenal cyst
+BMGC_DS11195,BMG_DS039481,OROFACIAL CLEFT 8
+BMGC_DS11196,BMG_DS039482,ECHO VIRUS 11 SENSITIVITY
+BMGC_DS11197,BMG_DS039483,"earring holes, natural"
+BMGC_DS11198,BMG_DS039484,thickened earlobes-conductive deafness syndrome
+BMGC_DS11199,BMG_DS039485,ear without helix
+BMGC_DS11200,BMG_DS039486,"ear pits, posterior helical"
+BMGC_DS11201,BMG_DS039487,ear folding
+BMGC_DS11202,BMG_DS039488,"ear antitragus, tag at base of"
+BMGC_DS11203,BMG_DS039489,Dopa-Responsive Dystonia
+BMGC_DS11204,BMG_DS039491,Paroxysmal choreoathetosis
+BMGC_DS11205,BMG_DS039492,Dystonia musculorum deformans 4
+BMGC_DS11206,BMG_DS039493,"DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT"
+BMGC_DS11207,BMG_DS039494,Dystelephalangy
+BMGC_DS11208,BMG_DS039498,"dyslexia, susceptibility to, 1"
+BMGC_DS11209,BMG_DS039502,"Dwarfism, Levi Type"
+BMGC_DS11210,BMG_DS039503,Dwarfism tall vertebrae
+BMGC_DS11211,BMG_DS039506,"Duodenal Ulcer, Hyperpepsinogenemic I"
+BMGC_DS11212,BMG_DS039507,Duodenal ulcer due to antral G-cell hyperfunction
+BMGC_DS11213,BMG_DS039508,Doughnut lesion of calvaria and bone fragility syndrome
+BMGC_DS11214,BMG_DS039509,double nail for fifth toe
+BMGC_DS11215,BMG_DS039511,Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature
+BMGC_DS11216,BMG_DS039514,"discrimination, Two-point, reduction 1N"
+BMGC_DS11217,BMG_DS039515,Digitotalar Dysmorphism
+BMGC_DS11218,BMG_DS039516,"diastema, dental medial"
+BMGC_DS11219,BMG_DS039518,"DIABETES MELLITUS, INSULIN-DEPENDENT, 2"
+BMGC_DS11220,BMG_DS039519,"Maturity-Onset Diabetes of the Young, Type 1"
+BMGC_DS11221,BMG_DS039520,KERATOSIS PALMOPLANTARIS STRIATA II
+BMGC_DS11222,BMG_DS039521,Dermoodontodysplasia
+BMGC_DS11223,BMG_DS039522,Familial dermographism
+BMGC_DS11224,BMG_DS039523,DERMODISTORTIVE URTICARIA
+BMGC_DS11225,BMG_DS039524,isolated congenital adermatoglyphia
+BMGC_DS11226,BMG_DS039527,"Dermal Ridges, Patternless"
+BMGC_DS11227,BMG_DS039529,major affective disorder 1
+BMGC_DS11228,BMG_DS039530,Deoxyribose-5-Phosphate Aldolase Deficiency
+BMGC_DS11229,BMG_DS039531,Dentin dysplasia sclerotic bones
+BMGC_DS11230,BMG_DS039532,"Failure of Tooth Eruption, Primary"
+BMGC_DS11231,BMG_DS039533,Dementia-Parkinsonism With Non-Alzheimer Amyloid Plaques
+BMGC_DS11232,BMG_DS039537,Auditory neuropathy
+BMGC_DS11233,BMG_DS039539,Deafness with Anhidrotic Ectodermal Dysplasia
+BMGC_DS11234,BMG_DS039540,"Deafness, Sensorineural, with Peripheral Neuropathy and Arterial Disease"
+BMGC_DS11235,BMG_DS039541,"Deafness, Autosomal Dominant 1"
+BMGC_DS11236,BMG_DS039542,"Deafness, Mid-Tone Neural"
+BMGC_DS11237,BMG_DS039544,Darwinian tubercle of pinna
+BMGC_DS11238,BMG_DS039545,"Darier Disease, Acral Hemorrhagic Type"
+BMGC_DS11239,BMG_DS039546,"Darier Disease, Segmental"
+BMGC_DS11240,BMG_DS039548,Mitochondrial Complex III Deficiency
+BMGC_DS11241,BMG_DS039549,Mitochondrial encephalopathy
+BMGC_DS11242,BMG_DS039552,Cutis Gyrata Syndrome of Beare And Stevenson
+BMGC_DS11243,BMG_DS039555,"CATARACT, COPPOCK-LIKE"
+BMGC_DS11244,BMG_DS039558,"Cryptophthalmos, Unilateral or Bilateral, Isolated"
+BMGC_DS11245,BMG_DS039560,"Cryptotia, Familial"
+BMGC_DS11246,BMG_DS039561,"Cryoglobulinemia, Familial Mixed"
+BMGC_DS11247,BMG_DS039562,"Cryofibrinogenemia, Familial Primary"
+BMGC_DS11248,BMG_DS039566,"CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT"
+BMGC_DS11249,BMG_DS039567,Craniofacial deafness hand syndrome
+BMGC_DS11250,BMG_DS039568,Cranioacrofacial Syndrome
+BMGC_DS11251,BMG_DS039569,Coxoauricular Syndrome
+BMGC_DS11252,BMG_DS039572,congenitally short costocoracoid ligament
+BMGC_DS11253,BMG_DS039573,Corticosteroid-Binding Globulin Deficiency
+BMGC_DS11254,BMG_DS039574,"Coronary Artery Dissection, Spontaneous"
+BMGC_DS11255,BMG_DS039577,Epithelial Recurrent Erosion Dystrophy
+BMGC_DS11256,BMG_DS039578,"Corneal Dystrophy, Posterior Polymorphous, 1"
+BMGC_DS11257,BMG_DS039580,"cornea plana 1, autosomal dominant"
+BMGC_DS11258,BMG_DS039581,Cornea guttata with anterior polar cataract
+BMGC_DS11259,BMG_DS039582,"coracoclavicular joint, anomalous"
+BMGC_DS11260,BMG_DS039583,"Copper deficiency, familial benign"
+BMGC_DS11261,BMG_DS039584,"Febrile Convulsions, Familial, 1"
+BMGC_DS11262,BMG_DS039585,"seizures, benign familial neonatal, 2"
+BMGC_DS11263,BMG_DS039588,"Arthrogryposis, distal, type 2E"
+BMGC_DS11264,BMG_DS039589,"Complement Component 4, Partial Deficiency Of"
+BMGC_DS11265,BMG_DS039590,Branchiootic Syndrome 2
+BMGC_DS11266,BMG_DS039593,COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY
+BMGC_DS11267,BMG_DS039594,Papillorenal syndrome
+BMGC_DS11268,BMG_DS039595,coloboma of macula
+BMGC_DS11269,BMG_DS039596,"CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2"
+BMGC_DS11270,BMG_DS039598,Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia
+BMGC_DS11271,BMG_DS039599,Cornelia de Lange Syndrome 3
+BMGC_DS11272,BMG_DS039600,CEREBROOCULOFACIOSKELETAL SYNDROME 4
+BMGC_DS11273,BMG_DS039601,Cerebrooculofacioskeletal Syndrome 2
+BMGC_DS11274,BMG_DS039602,ALOPECIA AREATA 2
+BMGC_DS11275,BMG_DS039604,"Spinocerebellar Ataxia, Autosomal Recessive 8"
+BMGC_DS11276,BMG_DS039605,Severe congenital neutropenia
+BMGC_DS11277,BMG_DS039606,Noonan Syndrome 4
+BMGC_DS11278,BMG_DS039607,"NEPHROTIC SYNDROME, TYPE 3"
+BMGC_DS11279,BMG_DS039608,Neutral Lipid Storage Disease with Myopathy
+BMGC_DS11280,BMG_DS039609,BRACHYDACTYLY-SYNDACTYLY SYNDROME
+BMGC_DS11281,BMG_DS039610,Optic atrophy 5
+BMGC_DS11282,BMG_DS039612,"Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia"
+BMGC_DS11283,BMG_DS039613,"Macular Degeneration, Age-Related, 4"
+BMGC_DS11284,BMG_DS039614,JOUBERT SYNDROME 6
+BMGC_DS11285,BMG_DS039615,Nemaline Myopathy 7
+BMGC_DS11286,BMG_DS039617,Osteogenesis Imperfecta Type VII
+BMGC_DS11287,BMG_DS039620,Recurrent skin infections
+BMGC_DS11288,BMG_DS039624,cold-induced sweating syndrome 2
+BMGC_DS11289,BMG_DS039625,"Parkinson disease 13, autosomal dominant, susceptibility to"
+BMGC_DS11290,BMG_DS039627,RETINITIS PIGMENTOSA 35
+BMGC_DS11291,BMG_DS039628,"Pachygyria, frontotemporal"
+BMGC_DS11292,BMG_DS039629,"Deafness, Autosomal Recessive 67"
+BMGC_DS11293,BMG_DS039633,congenital primary aphakia
+BMGC_DS11294,BMG_DS039634,Sclerocornea
+BMGC_DS11295,BMG_DS039635,"SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT"
+BMGC_DS11296,BMG_DS039636,"DEAFNESS, AUTOSOMAL RECESSIVE 65"
+BMGC_DS11297,BMG_DS039637,SPINOCEREBELLAR ATAXIA 28
+BMGC_DS11298,BMG_DS039638,SPINOCEREBELLAR ATAXIA 23
+BMGC_DS11299,BMG_DS039639,"Spastic Paraplegia 33, Autosomal Dominant"
+BMGC_DS11300,BMG_DS039642,Seborrhea-Like Dermatitis with Psoriasiform Elements
+BMGC_DS11301,BMG_DS039643,"HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY"
+BMGC_DS11302,BMG_DS039644,"Deafness, Autosomal Recessive 28"
+BMGC_DS11303,BMG_DS039645,Bleeding Disorder Due To P2RY12 Defect
+BMGC_DS11304,BMG_DS039646,"Erythrocytosis, Familial, 3"
+BMGC_DS11305,BMG_DS039648,Zygodactyly 1
+BMGC_DS11306,BMG_DS039649,"Spondylocostal Dysostosis 3, Autosomal Recessive"
+BMGC_DS11307,BMG_DS039650,"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 8, WITH EXOCRINE DYSFUNCTION"
+BMGC_DS11308,BMG_DS039651,"Hamartoma, Precalcaneal Congenital Fibrolipomatous"
+BMGC_DS11309,BMG_DS039652,"Generalized Epilepsy With Febrile Seizures Plus, Type 4"
+BMGC_DS11310,BMG_DS039653,"Peeling skin syndrome, acral type"
+BMGC_DS11311,BMG_DS039656,"aortic aneurysm, familial abdominal, 1"
+BMGC_DS11312,BMG_DS039657,maturity-onset diabetes of the young type 6
+BMGC_DS11313,BMG_DS039658,mega-cisterna magna
+BMGC_DS11314,BMG_DS039659,"Interleukin 2 Receptor, Alpha, Deficiency of"
+BMGC_DS11315,BMG_DS039660,Primary lateral sclerosis juvenile
+BMGC_DS11316,BMG_DS039661,INFLAMMATORY BOWEL DISEASE 5
+BMGC_DS11317,BMG_DS039662,"Heterotaxy, Visceral, 3, Autosomal"
+BMGC_DS11318,BMG_DS039663,"PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET"
+BMGC_DS11319,BMG_DS039664,"Deafness, Autosomal Dominant 24"
+BMGC_DS11320,BMG_DS039665,PAGET DISEASE OF BONE 4
+BMGC_DS11321,BMG_DS039666,"Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism"
+BMGC_DS11322,BMG_DS039667,22q13.3 Deletion Syndrome
+BMGC_DS11323,BMG_DS039668,"Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations"
+BMGC_DS11324,BMG_DS039669,"atrioventricular septal defect, susceptibility to, 2"
+BMGC_DS11325,BMG_DS039670,"Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome"
+BMGC_DS11326,BMG_DS039677,Genitopatellar Syndrome
+BMGC_DS11327,BMG_DS039680,Neuroferritinopathy
+BMGC_DS11328,BMG_DS039682,Fryns-Aftimos Syndrome
+BMGC_DS11329,BMG_DS039683,"Anemia, Diamond-Blackfan, 2"
+BMGC_DS11330,BMG_DS039684,"Goiter, Multinodular 3"
+BMGC_DS11331,BMG_DS039685,Rippling muscle disease
+BMGC_DS11332,BMG_DS039686,"Hereditary Motor And Sensory Neuropathy, Type IIC"
+BMGC_DS11333,BMG_DS039687,distal myopathy with vocal cord weakness
+BMGC_DS11334,BMG_DS039688,"HEMOCHROMATOSIS, TYPE 4"
+BMGC_DS11335,BMG_DS039689,"Congenital Disorder Of Glycosylation, Type IIB"
+BMGC_DS11336,BMG_DS039690,INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY
+BMGC_DS11337,BMG_DS039692,"Deafness, Autosomal Dominant 18"
+BMGC_DS11338,BMG_DS039693,"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2"
+BMGC_DS11339,BMG_DS039695,Familial Wilms tumor 2
+BMGC_DS11340,BMG_DS039696,Acropectoral syndrome
+BMGC_DS11341,BMG_DS039701,Holoprosencephaly 6
+BMGC_DS11342,BMG_DS039703,"Parkinson Disease 6, Autosomal Recessive Early-Onset"
+BMGC_DS11343,BMG_DS039704,"Cardiomyopathy, Dilated, with Left Ventricular Noncompaction"
+BMGC_DS11344,BMG_DS039705,Dimethylglycine Dehydrogenase Deficiency
+BMGC_DS11345,BMG_DS039710,"Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant"
+BMGC_DS11346,BMG_DS039711,"Spondyloocular Syndrome, Autosomal Recessive"
+BMGC_DS11347,BMG_DS039712,NONAKA MYOPATHY
+BMGC_DS11348,BMG_DS039713,"DEAFNESS, AUTOSOMAL RECESSIVE 27"
+BMGC_DS11349,BMG_DS039714,"CITRULLINEMIA, TYPE II, NEONATAL-ONSET"
+BMGC_DS11350,BMG_DS039715,Birdshot Chorioretinopathy
+BMGC_DS11351,BMG_DS039716,"DERMATITIS, ATOPIC, 4"
+BMGC_DS11352,BMG_DS039718,"Dermatitis, Atopic, 2"
+BMGC_DS11353,BMG_DS039720,"SEIZURES, BENIGN FAMILIAL INFANTILE, 2"
+BMGC_DS11354,BMG_DS039721,EXUDATIVE VITREORETINOPATHY 3
+BMGC_DS11355,BMG_DS039725,"Cataract, Central Saccular, With Sutural Opacities"
+BMGC_DS11356,BMG_DS039726,OTOSCLEROSIS 2
+BMGC_DS11357,BMG_DS039727,"Spinal muscular atrophy, Jerash type"
+BMGC_DS11358,BMG_DS039728,"SPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE"
+BMGC_DS11359,BMG_DS039730,Cardiomyopathy dilated with woolly hair and keratoderma
+BMGC_DS11360,BMG_DS039732,Late-Onset Retinal Degeneration
+BMGC_DS11361,BMG_DS039734,"myopathy, proximal, and ophthalmoplegia"
+BMGC_DS11362,BMG_DS039735,"Hyperaldosteronism, Familial, Type II"
+BMGC_DS11363,BMG_DS039736,Cerebrooculonasal Syndrome
+BMGC_DS11364,BMG_DS039738,"psoriasis 7, susceptibility to"
+BMGC_DS11365,BMG_DS039740,"Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1"
+BMGC_DS11366,BMG_DS039741,"Charcot-Marie-Tooth disease, Type 2B2"
+BMGC_DS11367,BMG_DS039742,"Charcot-Marie-Tooth disease, Type 2B1"
+BMGC_DS11368,BMG_DS039743,"Deafness, Autosomal Dominant 25"
+BMGC_DS11369,BMG_DS039744,"Cardiomyopathy, Dilated, 1K"
+BMGC_DS11370,BMG_DS039745,abdominal obesity-metabolic syndrome quantitative trait locus 2
+BMGC_DS11371,BMG_DS039746,Cone-Rod Dystrophy 8
+BMGC_DS11372,BMG_DS039748,"Parkinson Disease 4, Autosomal Dominant Lewy Body"
+BMGC_DS11373,BMG_DS039749,"ALZHEIMER DISEASE 6, LATE-ONSET"
+BMGC_DS11374,BMG_DS039752,Leber Congenital Amaurosis 6
+BMGC_DS11375,BMG_DS039753,Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia
+BMGC_DS11376,BMG_DS039754,"DEAFNESS, AUTOSOMAL RECESSIVE 26"
+BMGC_DS11377,BMG_DS039756,Hypotrichosis simplex
+BMGC_DS11378,BMG_DS039757,"Cataract, posterior polar, 3"
+BMGC_DS11379,BMG_DS039758,"Epilepsy, Nocturnal Frontal Lobe, Type 3"
+BMGC_DS11380,BMG_DS039759,PARAGANGLIOMAS 3
+BMGC_DS11381,BMG_DS039763,"Cardiomyopathy, Dilated, 1J"
+BMGC_DS11382,BMG_DS039764,Spinocerebellar ataxia 14
+BMGC_DS11383,BMG_DS039765,nemaline myopathy 5
+BMGC_DS11384,BMG_DS039766,Frontoocular Syndrome
+BMGC_DS11385,BMG_DS039768,MACROCEPHALY/AUTISM SYNDROME
+BMGC_DS11386,BMG_DS039769,Optic Atrophy 4
+BMGC_DS11387,BMG_DS039770,SPLIT-HAND/FOOT MALFORMATION 4
+BMGC_DS11388,BMG_DS039771,"Neuropathy, hereditary motor and sensory, Russe type"
+BMGC_DS11389,BMG_DS039772,Tuberous Sclerosis 1
+BMGC_DS11390,BMG_DS039773,Temtamy preaxial brachydactyly syndrome
+BMGC_DS11391,BMG_DS039774,"Spastic paraplegia 13, autosomal dominant"
+BMGC_DS11392,BMG_DS039775,Noonan Syndrome 2
+BMGC_DS11393,BMG_DS039776,"Mesomelic Dysplasia, Savarirayan Type"
+BMGC_DS11394,BMG_DS039777,Spinocerebellar ataxia 13
+BMGC_DS11395,BMG_DS039778,"Carney Complex, Type 2"
+BMGC_DS11396,BMG_DS039779,"Spastic paraplegia 14, autosomal recessive"
+BMGC_DS11397,BMG_DS039781,"systemic lupus erythematosus, susceptibility to, 2"
+BMGC_DS11398,BMG_DS039782,"DEAFNESS, AUTOSOMAL DOMINANT 23"
+BMGC_DS11399,BMG_DS039783,Wiedemann Steiner syndrome
+BMGC_DS11400,BMG_DS039784,"Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy"
+BMGC_DS11401,BMG_DS039786,"Muscular Dystrophy, Adult-Onset, with Leukoencephalopathy"
+BMGC_DS11402,BMG_DS039788,LETHAL CONGENITAL CONTRACTURE SYNDROME 1
+BMGC_DS11403,BMG_DS039789,"MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE"
+BMGC_DS11404,BMG_DS039795,Mucolipidosis III Gamma
+BMGC_DS11405,BMG_DS039798,Monosomy 7 of Bone Marrow
+BMGC_DS11406,BMG_DS039799,Monocyte Chemotactic Disorder
+BMGC_DS11407,BMG_DS039800,"Molybdenum Cofactor Deficiency, Complementation Group A"
+BMGC_DS11408,BMG_DS039801,"Molybdenum Cofactor Deficiency, Complementation Group B"
+BMGC_DS11409,BMG_DS039802,"Molybdenum Cofactor Deficiency, Complementation Group C"
+BMGC_DS11410,BMG_DS039803,Mitochondrial Complex II Deficiency
+BMGC_DS11411,BMG_DS039805,Mitochondrial myopathy with lactic acidosis
+BMGC_DS11412,BMG_DS039806,Mitochondrial Myopathy with a Defect in Mitochondrial Protein Transport
+BMGC_DS11413,BMG_DS039808,"MICROPHTHALMIA, ISOLATED 1"
+BMGC_DS11414,BMG_DS039809,"Microphthalmia, Isolated, with Coloboma 4"
+BMGC_DS11415,BMG_DS039811,ATAXIA-TELANGIECTASIA VARIANT V2
+BMGC_DS11416,BMG_DS039813,Microcephaly with Chemotactic Defect and Transient Hypogammaglobulinemia
+BMGC_DS11417,BMG_DS039814,Microcephaly-Micromelia Syndrome
+BMGC_DS11418,BMG_DS039815,Winship Viljoen Leary syndrome
+BMGC_DS11419,BMG_DS039816,"microcephaly 1, primary, autosomal recessive"
+BMGC_DS11420,BMG_DS039818,Methylmalonyl-CoA Epimerase Deficiency
+BMGC_DS11421,BMG_DS039820,Methylmalonic aciduria cblB type
+BMGC_DS11422,BMG_DS039821,Methylmalonic aciduria cblA type
+BMGC_DS11423,BMG_DS039822,Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency
+BMGC_DS11424,BMG_DS039823,"Methylmalonic Aciduria, mut(0) Type"
+BMGC_DS11425,BMG_DS039824,"Methylmalonic Aciduria, mut(-) Type"
+BMGC_DS11426,BMG_DS039825,Methylmalonic aciduria
+BMGC_DS11427,BMG_DS039826,3-Methylglutaconic Aciduria Type IV
+BMGC_DS11428,BMG_DS039827,"Methylcobalamin Deficiency, CblG Type"
+BMGC_DS11429,BMG_DS039828,Roy Maroteaux Kremp syndrome
+BMGC_DS11430,BMG_DS039830,"Metaphyseal Dysostosis, Mental Retardation, and Conductive Deafness"
+BMGC_DS11431,BMG_DS039831,early-onset anterior polar cataract
+BMGC_DS11432,BMG_DS039832,Metaphyseal Chondrodysplasia with Retinitis Pigmentosa
+BMGC_DS11433,BMG_DS039833,"Metaphyseal Chondrodysplasia, Pena Type"
+BMGC_DS11434,BMG_DS039835,"Spondylometaphyseal dysplasia, Sedaghatian type"
+BMGC_DS11435,BMG_DS039837,Pseudoarylsulfatase A Deficiency
+BMGC_DS11436,BMG_DS039838,Mesomelic Limb Shortening and Bowing
+BMGC_DS11437,BMG_DS039841,"intellectual disability, autosomal recessive 1"
+BMGC_DS11438,BMG_DS039842,Ter Haar syndrome
+BMGC_DS11439,BMG_DS039843,Megalencephaly with Dysmyelination
+BMGC_DS11440,BMG_DS039844,Megaepiphyseal dwarfism
+BMGC_DS11441,BMG_DS039846,MAST SYNDROME
+BMGC_DS11442,BMG_DS039850,"Maple Syrup Urine Disease, Type IA"
+BMGC_DS11443,BMG_DS039851,"MAPLE SYRUP URINE DISEASE, TYPE II"
+BMGC_DS11444,BMG_DS039855,Marles Greenberg Persaud syndrome
+BMGC_DS11445,BMG_DS039857,"Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive"
+BMGC_DS11446,BMG_DS039859,"magnesium, elevated red cell"
+BMGC_DS11447,BMG_DS039860,Stargardt Disease 1
+BMGC_DS11448,BMG_DS039861,"Hypomagnesemia 5, Renal, with Ocular Involvement"
+BMGC_DS11449,BMG_DS039864,"Lymphopenic Hypergammaglobulinemia, Antibody Deficiency, Autoimmune Hemolytic Anemia, and Glomerulonephritis"
+BMGC_DS11450,BMG_DS039865,Lymphokine Deficiency
+BMGC_DS11451,BMG_DS039866,"lymphoblastic leukemia, acute, with lymphomatous features"
+BMGC_DS11452,BMG_DS039868,"Lymphoblastic Transformation, Intrinsic Defect in"
+BMGC_DS11453,BMG_DS039870,chronic mucocutaneous candidiasis due to inhibition of lymphoblastic transformation
+BMGC_DS11454,BMG_DS039871,Dahlberg Borer Newcomer syndrome
+BMGC_DS11455,BMG_DS039872,Lipase deficiency combined
+BMGC_DS11456,BMG_DS039873,"Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome"
+BMGC_DS11457,BMG_DS039874,"Limb Defects, Distal Transverse, with Mental Retardation and Spasticity"
+BMGC_DS11458,BMG_DS039876,"Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis"
+BMGC_DS11459,BMG_DS039877,"leukemia, acute myelocytic, with polyposis coli and colon cancer"
+BMGC_DS11460,BMG_DS039878,"Leg, Absence Deformity of, with Congenital Cataract"
+BMGC_DS11461,BMG_DS039879,"Larsen like syndrome, lethal type"
+BMGC_DS11462,BMG_DS039880,Laron syndrome type 2
+BMGC_DS11463,BMG_DS039881,Lambotte syndrome
+BMGC_DS11464,BMG_DS039882,Lambert syndrome
+BMGC_DS11465,BMG_DS039883,Lactic Aciduria due to D-Lactic Acid
+BMGC_DS11466,BMG_DS039884,Pyruvate Dehydrogenase E3-Binding Protein Deficiency
+BMGC_DS11467,BMG_DS039885,Pyruvate Dehydrogenase E2 Deficiency
+BMGC_DS11468,BMG_DS039886,Erythrocyte Lactate Transporter Defect
+BMGC_DS11469,BMG_DS039887,"KURU, SUSCEPTIBILITY TO"
+BMGC_DS11470,BMG_DS039890,Keutel syndrome
+BMGC_DS11471,BMG_DS039892,HAIM-MUNK SYNDROME
+BMGC_DS11472,BMG_DS039893,"Keratoderma, Palmoplantar, Norrbotten Recessive Type"
+BMGC_DS11473,BMG_DS039894,Keratoconus posticus circumscriptus
+BMGC_DS11474,BMG_DS039897,"KENNY-CAFFEY SYNDROME, TYPE 1"
+BMGC_DS11475,BMG_DS039898,Kaufman oculocerebrofacial syndrome
+BMGC_DS11476,BMG_DS039899,Arima syndrome
+BMGC_DS11477,BMG_DS039900,"Nephronophthisis, familial juvenile"
+BMGC_DS11478,BMG_DS039901,Jejunal Atresia with Microcephaly and Ocular Anomalies
+BMGC_DS11479,BMG_DS039902,"isovaleric acid, inability to smell"
+BMGC_DS11480,BMG_DS039903,"Intrinsic Factor and R Binder, Combined Congenital Deficiency of"
+BMGC_DS11481,BMG_DS039904,BARAITSER-WINTER SYNDROME 1
+BMGC_DS11482,BMG_DS039905,Intestinal Pseudoobstruction with Patent Ductus Arteriosus and Natal Teeth
+BMGC_DS11483,BMG_DS039906,Neuronal intestinal pseudoobstruction
+BMGC_DS11484,BMG_DS039907,IMMUNODEFICIENCY WITH DEFECTIVE T-CELL RESPONSE TO INTERLEUKIN 1
+BMGC_DS11485,BMG_DS039908,"internal carotid arteries, hypoplasia of"
+BMGC_DS11486,BMG_DS039909,"Inosine Phosphorylase Deficiency, Immune Defect Due To"
+BMGC_DS11487,BMG_DS039910,Indolylacroyl Glycinuria with Mental Retardation
+BMGC_DS11488,BMG_DS039911,"Indifference to Pain, Congenital, Autosomal Recessive"
+BMGC_DS11489,BMG_DS039912,"immunoglobulin d level in plasma, low"
+BMGC_DS11490,BMG_DS039915,Absent corpus callosum cataract immunodeficiency
+BMGC_DS11491,BMG_DS039916,"Ichthyosis, Split Hairs, and Amino Aciduria"
+BMGC_DS11492,BMG_DS039917,"Ichthyosis, mental retardation, dwarfism, and renal impairment"
+BMGC_DS11493,BMG_DS039918,Jagell Holmgren Hofer syndrome
+BMGC_DS11494,BMG_DS039919,Self-Healing Collodion Baby
+BMGC_DS11495,BMG_DS039920,"Hypouricemia, Hypercalcinuria, and Decreased Bone Density"
+BMGC_DS11496,BMG_DS039921,Bamforth syndrome
+BMGC_DS11497,BMG_DS039922,"Hypoproteinemia, Hypercatabolic"
+BMGC_DS11498,BMG_DS039925,"Hypoparathyroidism, intellectual disability, dysmorphism syndrome"
+BMGC_DS11499,BMG_DS039927,hypomandibular faciocranial dysostosis
+BMGC_DS11500,BMG_DS039928,"Bartter syndrome, antenatal , type 2"
+BMGC_DS11501,BMG_DS039929,Hypohidrosis with Abnormal Palmar Dermal Ridges
+BMGC_DS11502,BMG_DS039930,Hypogonadism with Low-Grade Mental Deficiency and Microcephaly
+BMGC_DS11503,BMG_DS039931,HYPOGONADISM-CATARACT SYNDROME
+BMGC_DS11504,BMG_DS039932,"Glycogen Storage Disease 0, Liver"
+BMGC_DS11505,BMG_DS039933,"Polyglandular Deficiency Syndrome, Persian-Jewish Type"
+BMGC_DS11506,BMG_DS039934,"Autoimmune Polyendocrinopathy Syndrome, Type I, Autosomal Dominant"
+BMGC_DS11507,BMG_DS039936,"Hyperuricemia, Infantile, with Abnormal Behavior and Normal Hypoxanthine Guanine Phosphoribosyltransferase"
+BMGC_DS11508,BMG_DS039937,Hypertrophic Neuropathy And Cataract
+BMGC_DS11509,BMG_DS039938,X-linked congenital generalized hypertrichosis
+BMGC_DS11510,BMG_DS039939,"Hypertrichosis, Congenital Anterior Cervical, with Peripheral Sensory and Motor Neuropathy"
+BMGC_DS11511,BMG_DS039940,Hypertelorism and tetralogy of Fallot
+BMGC_DS11512,BMG_DS039941,Naguib-Richieri-Costa syndrome
+BMGC_DS11513,BMG_DS039943,Hyperphosphatasemia with intellectual disability
+BMGC_DS11514,BMG_DS039944,"Hyperparathyroidism, Neonatal Self-Limited Primary, With Hypercalciuria"
+BMGC_DS11515,BMG_DS039945,"hyperopia, high"
+BMGC_DS11516,BMG_DS039947,Hyperlysinemia Due To Defect In Lysine Transport Into Mitochondria
+BMGC_DS11517,BMG_DS039948,hyperlexia
+BMGC_DS11518,BMG_DS039949,seizures-intellectual disability due to hydroxylysinuria syndrome
+BMGC_DS11519,BMG_DS039950,L-2-HYDROXYGLUTARIC ACIDURIA
+BMGC_DS11520,BMG_DS039952,HYDROLETHALUS SYNDROME 1
+BMGC_DS11521,BMG_DS039953,Daish Hardman Lamont syndrome
+BMGC_DS11522,BMG_DS039955,Hydranencephaly with Renal Aplasia-Dysplasia
+BMGC_DS11523,BMG_DS039956,HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME
+BMGC_DS11524,BMG_DS039957,Humeroradial Multiple Synostosis Syndrome
+BMGC_DS11525,BMG_DS039958,"Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type"
+BMGC_DS11526,BMG_DS039960,Methylenetetrahydrofolate reductase deficiency
+BMGC_DS11527,BMG_DS039961,Holzgreve Wagner Rehder syndrome
+BMGC_DS11528,BMG_DS039962,Al Gazali Hirschsprung syndrome
+BMGC_DS11529,BMG_DS039963,"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"
+BMGC_DS11531,BMG_DS039965,Mowat-Wilson syndrome
+BMGC_DS11532,BMG_DS039966,"Bile acid synthesis defect, congenital, 2"
+BMGC_DS11533,BMG_DS039967,Hepatic venoocclusive disease with immunodeficiency
+BMGC_DS11534,BMG_DS039969,Hemolytic Anemia with Thermal Sensitivity of Red Cells
+BMGC_DS11535,BMG_DS039970,Urioste Martinez-Frias syndrome
+BMGC_DS11536,BMG_DS039971,"HEMIHYPERPLASIA, ISOLATED"
+BMGC_DS11537,BMG_DS039972,Deafness enamel hypoplasia nail defects
+BMGC_DS11538,BMG_DS039973,Kleiner Holmes syndrome
+BMGC_DS11539,BMG_DS039974,Hall Riggs mental retardation syndrome
+BMGC_DS11540,BMG_DS039975,Hair defect with photosensitivity and mental retardation
+BMGC_DS11541,BMG_DS039977,Grouped Pigmentation of the Macula
+BMGC_DS11542,BMG_DS039978,"Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II"
+BMGC_DS11543,BMG_DS039979,"Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I"
+BMGC_DS11544,BMG_DS039980,"GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 4"
+BMGC_DS11545,BMG_DS039981,Granulomatous Disease with Defect in Neutrophil Chemotaxis
+BMGC_DS11546,BMG_DS039982,Granulocytopenia with Immunoglobulin Abnormality
+BMGC_DS11547,BMG_DS039984,"46,XY sex reversal 7"
+BMGC_DS11548,BMG_DS039985,GOMBO syndrome
+BMGC_DS11549,BMG_DS039986,Glycoprotein Storage Disease
+BMGC_DS11550,BMG_DS039987,"GSD IV, Classic Hepatic"
+BMGC_DS11551,BMG_DS039989,"GSD IV, Neuromuscular Form, Fatal Perinatal"
+BMGC_DS11552,BMG_DS039990,"GSD IV, Neuromuscular Form, Congenital"
+BMGC_DS11553,BMG_DS039991,"GSD IV, Neuromuscular Form, Childhood"
+BMGC_DS11554,BMG_DS039994,"Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to"
+BMGC_DS11555,BMG_DS039995,Glutaric Aciduria IIA
+BMGC_DS11556,BMG_DS039996,Glutaric Aciduria IIB
+BMGC_DS11557,BMG_DS039997,Glutaric Aciduria IIC
+BMGC_DS11558,BMG_DS039998,"GLAUCOMA 3, PRIMARY CONGENITAL, A"
+BMGC_DS11559,BMG_DS040001,"Bernard-Soulier Syndrome, Type B"
+BMGC_DS11560,BMG_DS040002,"Bernard-Soulier Syndrome, Type C"
+BMGC_DS11561,BMG_DS040003,ghosal hematodiaphyseal dysplasia
+BMGC_DS11562,BMG_DS040004,Genito palato cardiac syndrome
+BMGC_DS11563,BMG_DS040005,"Gaucher Disease, Type Iiic"
+BMGC_DS11564,BMG_DS040009,"Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to"
+BMGC_DS11565,BMG_DS040010,Fructose and Galactose Intolerance
+BMGC_DS11566,BMG_DS040012,FRIEDREICH ATAXIA 1
+BMGC_DS11567,BMG_DS040014,Fraser-Like Syndrome
+BMGC_DS11568,BMG_DS040015,"Follicle-stimulating hormone deficiency, isolated"
+BMGC_DS11569,BMG_DS040016,"Fleck Retina, Familial Benign"
+BMGC_DS11570,BMG_DS040017,"Kininogen Deficiency, Total"
+BMGC_DS11571,BMG_DS040019,Fuhrmann syndrome
+BMGC_DS11572,BMG_DS040020,Fibular hypoplasia and complex brachydactyly
+BMGC_DS11573,BMG_DS040023,Femur bifid with monodactylous ectrodactyly
+BMGC_DS11574,BMG_DS040027,Autosomal recessive facio-digito-genital syndrome
+BMGC_DS11575,BMG_DS040028,"Factor V And Factor VIII, Combined Deficiency Of, With Normal Protein C And Protein C Inhibitor"
+BMGC_DS11576,BMG_DS040029,combined deficiency of factor V and factor VIII
+BMGC_DS11577,BMG_DS040030,"Faciocardiomelic Dysplasia, Lethal"
+BMGC_DS11578,BMG_DS040031,Facial Dysmorphism with Multiple Malformations
+BMGC_DS11579,BMG_DS040034,"Eunuchoidism, familial hypogonadotropic"
+BMGC_DS11580,BMG_DS040035,congenital lethal erythroderma
+BMGC_DS11581,BMG_DS040036,Ermine phenotype
+BMGC_DS11582,BMG_DS040037,erythema of acral regions
+BMGC_DS11583,BMG_DS040039,"Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness"
+BMGC_DS11584,BMG_DS040040,Epilepsy telangiectasia
+BMGC_DS11585,BMG_DS040041,Epilepsy occipital calcifications
+BMGC_DS11586,BMG_DS040042,"Epilepsy, Photogenic, with Spastic Diplegia and Mental Retardation"
+BMGC_DS11587,BMG_DS040043,Epidermolysis Bullosa With Diaphragmatic Hernia
+BMGC_DS11588,BMG_DS040044,Epidermolysis bullosa with pyloric atresia
+BMGC_DS11589,BMG_DS040047,Endocardial Fibroelastosis and Coarctation of Abdominal Aorta
+BMGC_DS11590,BMG_DS040048,Encephaloclastic Proliferative Vasculopathy
+BMGC_DS11591,BMG_DS040050,Pontocerebellar hypoplasia type 4
+BMGC_DS11592,BMG_DS040052,"Encephalomalacia, Multilocular"
+BMGC_DS11593,BMG_DS040055,"Ehlers-Danlos syndrome, cardiac valvular form"
+BMGC_DS11594,BMG_DS040056,Ehlers-Danlos Syndrome with Platelet Dysfunction from Fibronectin Abnormality
+BMGC_DS11595,BMG_DS040057,Ectrodactyly-Polydactyly
+BMGC_DS11596,BMG_DS040058,"Ectodermal dysplasia, ectrodactyly, and macular dystrophy"
+BMGC_DS11597,BMG_DS040059,"Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia"
+BMGC_DS11598,BMG_DS040061,Ectodermal Dysplasia and Neurosensory Deafness
+BMGC_DS11599,BMG_DS040062,Schopf-Schulz-Passarge Syndrome
+BMGC_DS11600,BMG_DS040065,Dystonia musculorum deformans type 2
+BMGC_DS11601,BMG_DS040066,Dyssegmental dysplasia
+BMGC_DS11602,BMG_DS040068,"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1"
+BMGC_DS11603,BMG_DS040069,Dysautonomia like disorder
+BMGC_DS11604,BMG_DS040070,"Dwarfism, Proportionate, with Hip Dislocation"
+BMGC_DS11605,BMG_DS040071,"Dwarfism, Low-Birth-Weight Type, with Unresponsiveness to Growth Hormone"
+BMGC_DS11606,BMG_DS040072,Dohle bodies and leukemia
+BMGC_DS11607,BMG_DS040073,DK Phocomelia Syndrome
+BMGC_DS11608,BMG_DS040077,"Rhizomelic chondrodysplasia punctata, type 2"
+BMGC_DS11609,BMG_DS040078,"2,4-Dienoyl-CoA Reductase Deficiency"
+BMGC_DS11610,BMG_DS040079,Dicarboxylicaminoaciduria
+BMGC_DS11611,BMG_DS040080,"Diastrophic Dysplasia, Broad Bone-Platyspondylic Variant"
+BMGC_DS11612,BMG_DS040081,Trichohepatoenteric Syndrome
+BMGC_DS11613,BMG_DS040082,Donnai-Barrow syndrome
+BMGC_DS11614,BMG_DS040083,diaphragmatic hernia 2
+BMGC_DS11615,BMG_DS040084,Diaminopentanuria
+BMGC_DS11616,BMG_DS040085,"Diabetes Insipidus, Nephrogenic, with Mental Retardation and Intracerebral Calcification"
+BMGC_DS11617,BMG_DS040088,Dermatoleukodystrophy
+BMGC_DS11618,BMG_DS040089,polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly
+BMGC_DS11619,BMG_DS040090,"Deafness, Sensorineural, Autosomal-Mitochondrial Type"
+BMGC_DS11620,BMG_DS040091,Deafness oligodontia syndrome
+BMGC_DS11621,BMG_DS040092,"Deafness, Neural, with Atypical Atopic Dermatitis"
+BMGC_DS11622,BMG_DS040093,"Deafness, Neural, Congenital Moderate"
+BMGC_DS11623,BMG_DS040094,Groll Hirschowitz syndrome
+BMGC_DS11624,BMG_DS040095,"Deafness, Congenital, with Vitiligo and Achalasia"
+BMGC_DS11625,BMG_DS040096,Deafness conductive ptosis skeletal anomalies
+BMGC_DS11626,BMG_DS040097,"Deafness, Conductive, with Malformed External Ear"
+BMGC_DS11627,BMG_DS040099,"Deafness, Congenital, with Total Albinism"
+BMGC_DS11628,BMG_DS040100,Split-Hand-Foot Malformation With Sensorineural Hearing Loss
+BMGC_DS11629,BMG_DS040102,Dandy Walker malformation postaxial polydactyly
+BMGC_DS11630,BMG_DS040104,"Leigh syndrome , French Canadian type"
+BMGC_DS11631,BMG_DS040105,"Cystinuria, Type A"
+BMGC_DS11632,BMG_DS040106,"Cystinuria, Type B"
+BMGC_DS11633,BMG_DS040108,De Toni-Debre-Fanconi Syndrome
+BMGC_DS11634,BMG_DS040109,Cystic Kidney Disease with Ventriculomegaly
+BMGC_DS11635,BMG_DS040111,Cysteine Peptiduria
+BMGC_DS11636,BMG_DS040113,CUTIS VERTICIS GYRATA AND IMPAIRED INTELLECTUAL DEVELOPMENT
+BMGC_DS11637,BMG_DS040114,"Cutaneous photosensitivity and colitis, lethal"
+BMGC_DS11638,BMG_DS040115,Acth-Independent Macronodular Adrenal Hyperplasia
+BMGC_DS11639,BMG_DS040116,curved nail of fourth toe
+BMGC_DS11640,BMG_DS040118,Craniosynostosis Mental Retardation Clefting Syndrome
+BMGC_DS11641,BMG_DS040120,Craniosynostosis with Fibular Aplasia
+BMGC_DS11642,BMG_DS040123,Craniofacial dyssynostosis
+BMGC_DS11643,BMG_DS040124,Temtamy syndrome
+BMGC_DS11644,BMG_DS040125,"Cranial Nerves, Recurrent Paresis Of"
+BMGC_DS11645,BMG_DS040126,"Cranial Nerves, Congenital Paresis Of"
+BMGC_DS11646,BMG_DS040128,"cramps, familial adolescent"
+BMGC_DS11647,BMG_DS040130,congenital hereditary endothelial dystrophy of cornea
+BMGC_DS11648,BMG_DS040132,CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS
+BMGC_DS11649,BMG_DS040133,CORNEA PLANA 2
+BMGC_DS11650,BMG_DS040134,"Convulsive Disorder, Familial, with Prenatal or Early Onset"
+BMGC_DS11651,BMG_DS040135,"Contractures, Congenital, Torticollis, and Malignant Hyperthermia"
+BMGC_DS11652,BMG_DS040136,ADAM COMPLEX
+BMGC_DS11653,BMG_DS040139,Conotruncal cardiac defects
+BMGC_DS11654,BMG_DS040140,Orstavik Lindemann Solberg syndrome
+BMGC_DS11655,BMG_DS040141,Amaurosis hypertrichosis
+BMGC_DS11656,BMG_DS040143,Achromatopsia 2
+BMGC_DS11657,BMG_DS040144,Coloboma of Macula and Skeletal Anomalies
+BMGC_DS11658,BMG_DS040145,"COLLAGENOSIS, FAMILIAL REACTIVE PERFORATING"
+BMGC_DS11659,BMG_DS040147,COACH syndrome
+BMGC_DS11660,BMG_DS040148,Yunis Varon syndrome
+BMGC_DS11661,BMG_DS040149,Combined Oxidative Phosphorylation Deficiency 4
+BMGC_DS11662,BMG_DS040150,"Telangiectasia, Hereditary Hemorrhagic, Type 4"
+BMGC_DS11663,BMG_DS040152,"Anemia, Diamond-Blackfan, 3"
+BMGC_DS11664,BMG_DS040154,Hereditary Angioedema Type III
+BMGC_DS11665,BMG_DS040155,Leber Congenital Amaurosis 12
+BMGC_DS11666,BMG_DS040156,"DEAFNESS, AUTOSOMAL RECESSIVE 59"
+BMGC_DS11667,BMG_DS040157,Neurodegeneration With Brain Iron Accumulation 2B
+BMGC_DS11668,BMG_DS040159,"DEAFNESS, AUTOSOMAL RECESSIVE 66"
+BMGC_DS11669,BMG_DS040160,"migraine with or without aura, susceptibility to, 11"
+BMGC_DS11670,BMG_DS040161,"migraine with or without aura, susceptibility to, 10"
+BMGC_DS11671,BMG_DS040162,Alagille Syndrome 2
+BMGC_DS11672,BMG_DS040163,"Olivopontocerebellar hypoplasia, fetal-onset"
+BMGC_DS11673,BMG_DS040165,"Cataract, Pulverulent, Juvenile-Onset"
+BMGC_DS11674,BMG_DS040166,"Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism"
+BMGC_DS11675,BMG_DS040167,"3-@METHYLGLUTACONIC ACIDURIA, TYPE V"
+BMGC_DS11676,BMG_DS040168,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 10"
+BMGC_DS11677,BMG_DS040169,SENIOR-LOKEN SYNDROME 6
+BMGC_DS11678,BMG_DS040170,JOUBERT SYNDROME 5
+BMGC_DS11679,BMG_DS040171,diaphragmatic hernia 3
+BMGC_DS11680,BMG_DS040173,Immunodeficiency due to Defect in CD3-Zeta
+BMGC_DS11681,BMG_DS040174,"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2"
+BMGC_DS11682,BMG_DS040175,MORM syndrome
+BMGC_DS11683,BMG_DS040177,"Diabetes Mellitus, Insulin-Dependent, 19"
+BMGC_DS11684,BMG_DS040178,"DEAFNESS, AUTOSOMAL RECESSIVE 44"
+BMGC_DS11685,BMG_DS040179,"DEAFNESS, AUTOSOMAL RECESSIVE 49"
+BMGC_DS11686,BMG_DS040180,"Macular Degeneration, Age-Related, 7"
+BMGC_DS11687,BMG_DS040181,"DEAFNESS, AUTOSOMAL RECESSIVE 62"
+BMGC_DS11688,BMG_DS040182,Leber Congenital Amaurosis 10
+BMGC_DS11689,BMG_DS040184,"Heart-hand syndrome, Slovenian type"
+BMGC_DS11690,BMG_DS040187,Williams-Beuren Region Duplication Syndrome
+BMGC_DS11691,BMG_DS040188,"celiac disease, susceptibility to, 3"
+BMGC_DS11692,BMG_DS040190,"celiac disease, susceptibility to, 4"
+BMGC_DS11693,BMG_DS040193,"Cataract, Congenital Nuclear, Autosomal Recessive 2"
+BMGC_DS11694,BMG_DS040194,Proopiomelanocortin Deficiency
+BMGC_DS11695,BMG_DS040195,"SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT"
+BMGC_DS11696,BMG_DS040196,"Alzheimer Disease, Familial Early-Onset, With Coexisting Amyloid And Prion Pathology"
+BMGC_DS11697,BMG_DS040197,Brooke-Spiegler syndrome
+BMGC_DS11698,BMG_DS040201,"Diabetes Mellitus, Congenital Autoimmune"
+BMGC_DS11699,BMG_DS040202,"Hypobetalipoproteinemia, Familial, 2"
+BMGC_DS11700,BMG_DS040203,MICROHYDRANENCEPHALY
+BMGC_DS11701,BMG_DS040204,WOLFRAM SYNDROME 2
+BMGC_DS11702,BMG_DS040206,Becker Nevus Syndrome
+BMGC_DS11703,BMG_DS040207,Okamoto syndrome
+BMGC_DS11704,BMG_DS040208,schizophrenia 9
+BMGC_DS11705,BMG_DS040209,NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS
+BMGC_DS11706,BMG_DS040210,BARDET-BIEDL SYNDROME 6
+BMGC_DS11707,BMG_DS040211,ASTHMA AND NASAL POLYPS
+BMGC_DS11708,BMG_DS040212,"Retinal Dystrophy, Early Onset Severe"
+BMGC_DS11709,BMG_DS040214,"Stickler syndrome, type 2"
+BMGC_DS11710,BMG_DS040216,"Spastic paraplegia 12, autosomal dominant"
+BMGC_DS11711,BMG_DS040217,"Microcephaly, Primary Autosomal Recessive, 3"
+BMGC_DS11712,BMG_DS040218,Huntington disease-like 3
+BMGC_DS11713,BMG_DS040219,Caudate atrophy
+BMGC_DS11714,BMG_DS040220,"Muscular Dystrophy, Congenital, 1B"
+BMGC_DS11715,BMG_DS040221,"Ichthyosis, Nonlamellar and Nonerythrodermic, Congenital, Autosomal Recessive"
+BMGC_DS11716,BMG_DS040223,"CARDIOMYOPATHY, DILATED, 1I"
+BMGC_DS11717,BMG_DS040224,craniosynostosis 2
+BMGC_DS11718,BMG_DS040225,"Deafness, Autosomal Dominant 20"
+BMGC_DS11719,BMG_DS040229,"Bare Lymphocyte Syndrome, Type I"
+BMGC_DS11720,BMG_DS040230,"Charcot-Marie-Tooth disease, Type 4B2"
+BMGC_DS11721,BMG_DS040231,"Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma"
+BMGC_DS11722,BMG_DS040233,LEBER CONGENITAL AMAUROSIS 5
+BMGC_DS11723,BMG_DS040234,Ectodermal Dysplasia-Skin Fragility Syndrome
+BMGC_DS11724,BMG_DS040235,INFLAMMATORY BOWEL DISEASE 3
+BMGC_DS11725,BMG_DS040237,"Bile acid synthesis defect, congenital, 4"
+BMGC_DS11726,BMG_DS040238,"Neuropathy, hereditary motor and sensory, Okinawa type"
+BMGC_DS11727,BMG_DS040240,SPINOCEREBELLAR ATAXIA 11
+BMGC_DS11728,BMG_DS040242,pyogenic arthritis-pyoderma gangrenosum-acne syndrome
+BMGC_DS11729,BMG_DS040243,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 6"
+BMGC_DS11730,BMG_DS040244,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 5"
+BMGC_DS11731,BMG_DS040245,"colorectal cancer, hereditary nonpolyposis, type 7"
+BMGC_DS11732,BMG_DS040246,Leber Congenital Amaurosis 4
+BMGC_DS11733,BMG_DS040247,ataxia-telangiectasia-like disorder
+BMGC_DS11734,BMG_DS040248,NEPHRONOPHTHISIS 3
+BMGC_DS11735,BMG_DS040250,Patent Ductus Arteriosus and Bicuspid Aortic Valve with Hand Anomalies
+BMGC_DS11736,BMG_DS040252,"Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency"
+BMGC_DS11737,BMG_DS040253,"Epilepsy, Partial, with Variable Foci"
+BMGC_DS11738,BMG_DS040255,"Spastic paraplegia 11, autosomal recessive"
+BMGC_DS11739,BMG_DS040256,"febrile seizures, familial, 4"
+BMGC_DS11740,BMG_DS040257,"Advanced Sleep-Phase Syndrome, Familial"
+BMGC_DS11741,BMG_DS040259,Spinocerebellar Ataxia 12
+BMGC_DS11742,BMG_DS040260,"Acne, Adult"
+BMGC_DS11743,BMG_DS040261,"MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS11744,BMG_DS040262,SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1
+BMGC_DS11745,BMG_DS040263,"MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICAL MALFORMATIONS"
+BMGC_DS11746,BMG_DS040266,Blepharophimosis with Facial and Genital Anomalies and Mental Retardation
+BMGC_DS11747,BMG_DS040267,OVERLAP CONNECTIVE TISSUE DISEASE
+BMGC_DS11748,BMG_DS040268,"Rheumatoid Arthritis, Systemic Juvenile"
+BMGC_DS11749,BMG_DS040269,"ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3"
+BMGC_DS11750,BMG_DS040271,"Cardiomyopathy, Dilated, 1h"
+BMGC_DS11751,BMG_DS040272,Carney Triad
+BMGC_DS11752,BMG_DS040273,"Limb-girdle muscular dystrophy, type 2E"
+BMGC_DS11753,BMG_DS040274,"Short Stature, Idiopathic, Autosomal"
+BMGC_DS11754,BMG_DS040277,"HEMOCHROMATOSIS, TYPE 3"
+BMGC_DS11755,BMG_DS040278,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1"
+BMGC_DS11756,BMG_DS040279,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2"
+BMGC_DS11757,BMG_DS040280,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3"
+BMGC_DS11758,BMG_DS040281,Leber Congenital Amaurosis 3
+BMGC_DS11759,BMG_DS040282,"CATARACT, AUTOSOMAL DOMINANT"
+BMGC_DS11760,BMG_DS040283,Familial encephalopathy with neuroserpin inclusion bodies
+BMGC_DS11761,BMG_DS040284,Chudley-Mccullough syndrome
+BMGC_DS11762,BMG_DS040287,"Spastic paraplegia 10, autosomal dominant"
+BMGC_DS11763,BMG_DS040288,"Facial paresis, hereditary, congenital"
+BMGC_DS11764,BMG_DS040289,Poikiloderma with Neutropenia
+BMGC_DS11765,BMG_DS040291,left ventricular noncompaction 1
+BMGC_DS11766,BMG_DS040292,"Congenital Cataracts, Facial Dysmorphism, And Neuropathy"
+BMGC_DS11767,BMG_DS040294,"Cardiomyopathy, Dilated, 1g"
+BMGC_DS11768,BMG_DS040295,"Cerebellar Ataxia, Deafness, and Narcolepsy"
+BMGC_DS11769,BMG_DS040296,"Vohwinkel Syndrome, Variant Form"
+BMGC_DS11770,BMG_DS040297,Cone-Rod Dystrophy 3
+BMGC_DS11771,BMG_DS040298,"DEAFNESS, AUTOSOMAL RECESSIVE 20"
+BMGC_DS11772,BMG_DS040299,megalencephalic leukoencephalopathy with subcortical cysts
+BMGC_DS11773,BMG_DS040300,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2
+BMGC_DS11774,BMG_DS040301,"DEAFNESS, AUTOSOMAL DOMINANT 16"
+BMGC_DS11775,BMG_DS040304,"Autoimmune Lymphoproliferative Syndrome, Type IIA"
+BMGC_DS11776,BMG_DS040305,"Beta Thalassemia, Dominant Inclusion Body Type"
+BMGC_DS11777,BMG_DS040306,Childhood Ataxia with Central Nervous System Hypomyelinization
+BMGC_DS11778,BMG_DS040307,CCHS WITH HIRSCHSPRUNG DISEASE
+BMGC_DS11779,BMG_DS040308,LONG QT SYNDROME 3
+BMGC_DS11780,BMG_DS040310,"Cleidocranial Dysplasia, Recessive Form"
+BMGC_DS11781,BMG_DS040311,"Cleft Palate, Deafness, and Oligodontia"
+BMGC_DS11782,BMG_DS040312,Verloove-Vanhorick Brubakk syndrome
+BMGC_DS11783,BMG_DS040313,Novak syndrome
+BMGC_DS11784,BMG_DS040314,Citrulline transport defect
+BMGC_DS11785,BMG_DS040315,"COPPER TOXICOSIS, IDIOPATHIC"
+BMGC_DS11786,BMG_DS040316,Circumvallate Placenta Syndrome
+BMGC_DS11787,BMG_DS040318,Choroid plexus calcification with mental retardation
+BMGC_DS11788,BMG_DS040319,"Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism"
+BMGC_DS11789,BMG_DS040320,"Chorea, Benign Familial"
+BMGC_DS11790,BMG_DS040322,"Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome"
+BMGC_DS11791,BMG_DS040324,"RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1"
+BMGC_DS11792,BMG_DS040325,Chondrodysplasia Calcificans Metaphysealis
+BMGC_DS11793,BMG_DS040326,"Chondrodysplasia, blomstrand type"
+BMGC_DS11794,BMG_DS040329,"GRISCELLI SYNDROME, TYPE 1"
+BMGC_DS11795,BMG_DS040330,"Charcot-Marie-Tooth disease, Type 4A"
+BMGC_DS11796,BMG_DS040331,Klippel Feil syndrome recessive type
+BMGC_DS11797,BMG_DS040333,Cerebrofaciothoracic Dysplasia
+BMGC_DS11798,BMG_DS040335,Pelizaeus-Merzbacher like brain sclerosis
+BMGC_DS11799,BMG_DS040337,"Cerebral Angiopathy, Dysphoric"
+BMGC_DS11800,BMG_DS040338,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2"
+BMGC_DS11801,BMG_DS040339,Cerebellar Vermis Aplasia with Associated Features suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome
+BMGC_DS11802,BMG_DS040340,"Cerebellar Ataxia, Benign, with Thermoanalgesia"
+BMGC_DS11803,BMG_DS040341,Cerebellar Ataxia and Neurosensory Deafness
+BMGC_DS11804,BMG_DS040342,Cerebellar Ataxia and Hypogonadotropic Hypogonadism
+BMGC_DS11805,BMG_DS040344,Cephalin Lipidosis
+BMGC_DS11806,BMG_DS040345,PREMATURE CENTROMERE DIVISION
+BMGC_DS11807,BMG_DS040346,Syndactyly Cenani Lenz type
+BMGC_DS11808,BMG_DS040347,"celiac disease, susceptibility to, 1"
+BMGC_DS11809,BMG_DS040348,"Microphthalmia, Isolated, with Cataract 2"
+BMGC_DS11810,BMG_DS040350,Cataract and congenital ichthyosis
+BMGC_DS11811,BMG_DS040351,CATARACT-ALOPECIA-SCLERODACTYLY SYNDROME
+BMGC_DS11812,BMG_DS040352,Cataract and cardiomyopathy
+BMGC_DS11813,BMG_DS040353,Myopathic carnitine deficiency
+BMGC_DS11814,BMG_DS040355,Cardiomyopathy Associated With Myopathy And Sudden Death
+BMGC_DS11815,BMG_DS040356,Cardioauditory syndrome of Sanchez Cascos
+BMGC_DS11816,BMG_DS040358,Cardiac Septal Defects with Coarctation of the Aorta
+BMGC_DS11817,BMG_DS040359,"Cardiac Lipidosis, Familial"
+BMGC_DS11818,BMG_DS040360,"Candidiasis, Familial, 2"
+BMGC_DS11819,BMG_DS040361,Camptomelic syndrome long limb type
+BMGC_DS11820,BMG_DS040363,Tel Hashomer camptodactyly syndrome
+BMGC_DS11821,BMG_DS040365,Campomelia Cumming type
+BMGC_DS11822,BMG_DS040366,Calcification of Joints and Arteries
+BMGC_DS11823,BMG_DS040368,"Brachydactyly, Type A2, With Microcephaly"
+BMGC_DS11824,BMG_DS040371,Bowen-Conradi syndrome
+BMGC_DS11825,BMG_DS040373,"Blepharophimosis with ptosis, syndactyly, and short stature"
+BMGC_DS11826,BMG_DS040375,"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I"
+BMGC_DS11827,BMG_DS040376,Bird headed dwarfism Montreal type
+BMGC_DS11828,BMG_DS040377,BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY
+BMGC_DS11829,BMG_DS040378,Biemond syndrome II
+BMGC_DS11830,BMG_DS040379,3-methylcrotonyl CoA carboxylase 2 deficiency
+BMGC_DS11831,BMG_DS040380,"Beta-Aminoisobutyric Acid, Urinary Excretion of"
+BMGC_DS11832,BMG_DS040381,"Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification"
+BMGC_DS11833,BMG_DS040382,Beemer Ertbruggen syndrome
+BMGC_DS11834,BMG_DS040387,"Bare Lymphocyte Syndrome, Type II, Complementation Group B"
+BMGC_DS11835,BMG_DS040388,"Bare Lymphocyte Syndrome, Type II, Complementation Group C"
+BMGC_DS11836,BMG_DS040389,"Bare Lymphocyte Syndrome, Type II, Complementation Group D"
+BMGC_DS11837,BMG_DS040390,"Bare Lymphocyte Syndrome, Type II, Complementation Group E"
+BMGC_DS11838,BMG_DS040391,Bardet-Biedl syndrome 3
+BMGC_DS11839,BMG_DS040392,BARDET-BIEDL SYNDROME 7
+BMGC_DS11840,BMG_DS040393,BARDET-BIEDL SYNDROME 8
+BMGC_DS11841,BMG_DS040394,BARDET-BIEDL SYNDROME 9
+BMGC_DS11842,BMG_DS040395,BARDET-BIEDL SYNDROME 10
+BMGC_DS11843,BMG_DS040396,BARDET-BIEDL SYNDROME 11
+BMGC_DS11844,BMG_DS040397,BARDET-BIEDL SYNDROME 12
+BMGC_DS11845,BMG_DS040398,"Aural Atresia, Multiple Congenital Anomalies, and Mental Retardation"
+BMGC_DS11846,BMG_DS040399,ATRICHIA WITH PAPULAR LESIONS
+BMGC_DS11847,BMG_DS040400,Atonic-Astatic Syndrome of Foerster
+BMGC_DS11848,BMG_DS040401,"Athrombia, Essential"
+BMGC_DS11849,BMG_DS040402,"Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease"
+BMGC_DS11850,BMG_DS040403,"ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA"
+BMGC_DS11851,BMG_DS040405,"Ataxia, Deafness, and Cardiomyopathy"
+BMGC_DS11852,BMG_DS040406,Ataxia with Myoclonic Epilepsy and Presenile Dementia
+BMGC_DS11853,BMG_DS040407,"Asthma, Short Stature, and Elevated IgA"
+BMGC_DS11854,BMG_DS040408,"Asthma, Nasal Polyps, And Aspirin Intolerance"
+BMGC_DS11855,BMG_DS040409,CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME
+BMGC_DS11856,BMG_DS040411,Kuskokwim disease
+BMGC_DS11857,BMG_DS040412,Johnston Aarons Schelley syndrome
+BMGC_DS11858,BMG_DS040413,Arthrogryposis multiplex congenita whistling face
+BMGC_DS11859,BMG_DS040414,Arthrogryposis multiplex congenita neurogenic type
+BMGC_DS11860,BMG_DS040415,"Arthrogryposis, renal dysfunction, and cholestasis 1"
+BMGC_DS11861,BMG_DS040418,"Arteriosclerosis, Severe Juvenile"
+BMGC_DS11862,BMG_DS040419,ARTERIAL TORTUOSITY SYNDROME
+BMGC_DS11863,BMG_DS040420,Arterial calcification of infancy
+BMGC_DS11864,BMG_DS040421,"Coronary Sclerosis, Medial, of Infancy"
+BMGC_DS11865,BMG_DS040422,"Aplasia of Extensor Muscles of Fingers, Unilateral, with Generalized Polyneuropathy"
+BMGC_DS11866,BMG_DS040423,Aplasia cutis congenita intestinal lymphangiectasia
+BMGC_DS11867,BMG_DS040425,"Antithrombin, Familial Hemorrhagic Diathesis due to"
+BMGC_DS11868,BMG_DS040426,anosmia for isobutyric acid
+BMGC_DS11869,BMG_DS040428,"Microphthalmia, Syndromic 3"
+BMGC_DS11870,BMG_DS040429,Optic Nerve Hypoplasia and Abnormalities of the Central Nervous System
+BMGC_DS11871,BMG_DS040430,Aniridia renal agenesis psychomotor retardation
+BMGC_DS11872,BMG_DS040431,"Angiomatosis, diffuse corticomeningeal, of Divry and Van Bogaert"
+BMGC_DS11873,BMG_DS040432,"Angiolipomatosis, Familial"
+BMGC_DS11874,BMG_DS040433,"Anemia, Nonspherocytic Hemolytic, possibly due to Defect in Porphyrin Metabolism"
+BMGC_DS11875,BMG_DS040434,"Anemia, Nonspherocytic Hemolytic, associated with Abnormality of Red Cell Membrane"
+BMGC_DS11876,BMG_DS040436,Amyotrophic Lateral Sclerosis With Polyglucosan Bodies
+BMGC_DS11877,BMG_DS040437,"Amyotrophic Lateral Sclerosis, Juvenile, with Dementia"
+BMGC_DS11878,BMG_DS040438,"Amyotrophic Lateral Sclerosis 2, Juvenile"
+BMGC_DS11879,BMG_DS040439,"Amyloidosis of Gingiva and Conjunctiva, with Mental Retardation"
+BMGC_DS11880,BMG_DS040440,"Amobarbital, Deficient N-Hydroxylation of"
+BMGC_DS11881,BMG_DS040441,2-aminoadipic 2-oxoadipic aciduria
+BMGC_DS11882,BMG_DS040442,"Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis"
+BMGC_DS11883,BMG_DS040443,"Amaurosis congenita of Leber, type 2"
+BMGC_DS11884,BMG_DS040444,Alpha-2-Deficient Collagen Disease
+BMGC_DS11885,BMG_DS040445,alopecia universalis congenita
+BMGC_DS11886,BMG_DS040446,Alopecia-Mental Retardation Syndrome 1
+BMGC_DS11887,BMG_DS040447,Microcephaly albinism digital anomalies syndrome
+BMGC_DS11888,BMG_DS040448,Coloboma of Alar-nasal cartilages with telecanthus
+BMGC_DS11889,BMG_DS040450,"Neutropenia, Severe Congenital, Autosomal Dominant 1"
+BMGC_DS11890,BMG_DS040452,agenesis of cerebral white matter
+BMGC_DS11891,BMG_DS040453,"Hypodysfibrinogenemia, Congenital"
+BMGC_DS11892,BMG_DS040454,Adrenocortical Unresponsiveness To Acth With Postreceptor Defect
+BMGC_DS11893,BMG_DS040455,"adrenocortical carcinoma, hereditary"
+BMGC_DS11894,BMG_DS040456,"Adrenal Hypoplasia, Cytomegalic Type"
+BMGC_DS11895,BMG_DS040457,"Adrenal Hypoplasia, Congenital, With Absent Pituitary Luteinizing Hormone"
+BMGC_DS11896,BMG_DS040458,"Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency"
+BMGC_DS11897,BMG_DS040459,Antley-Bixler Syndrome with Disordered Steroidogenesis
+BMGC_DS11898,BMG_DS040460,Severe short-limb dwarfism
+BMGC_DS11899,BMG_DS040461,Acrofrontofacionasal dysostosis syndrome
+BMGC_DS11900,BMG_DS040462,Acrofacial dysostosis Rodriguez type
+BMGC_DS11901,BMG_DS040464,Elejalde Disease
+BMGC_DS11902,BMG_DS040465,Acrorenal mandibular syndrome
+BMGC_DS11903,BMG_DS040466,Ackerman syndrome
+BMGC_DS11904,BMG_DS040467,Short-Limb Skeletal Dysplasia with Severe Combined Immunodeficiency
+BMGC_DS11905,BMG_DS040468,Achalasia microcephaly
+BMGC_DS11906,BMG_DS040469,"Achalasia, familial esophageal"
+BMGC_DS11907,BMG_DS040470,Acanthosis nigricans muscle cramps acral enlargement
+BMGC_DS11908,BMG_DS040471,ABLEPHARON-MACROSTOMIA SYNDROME
+BMGC_DS11909,BMG_DS040472,"zinc, elevated plasma"
+BMGC_DS11910,BMG_DS040474,Woronets trait
+BMGC_DS11911,BMG_DS040475,autosomal dominant wooly hair
+BMGC_DS11912,BMG_DS040476,Wilms Tumor 3
+BMGC_DS11913,BMG_DS040477,"Whispering dysphonia, hereditary"
+BMGC_DS11914,BMG_DS040478,"WAARDENBURG SYNDROME, TYPE IIA"
+BMGC_DS11915,BMG_DS040480,Tucker syndrome
+BMGC_DS11916,BMG_DS040481,Snowflake vitreoretinal degeneration
+BMGC_DS11917,BMG_DS040482,"congenital vertical talus, bilateral"
+BMGC_DS11918,BMG_DS040483,Vertebral Hypoplasia With Lumbar Kyphosis
+BMGC_DS11919,BMG_DS040484,Vertebral fusion posterior lumbosacral blepharoptosis
+BMGC_DS11920,BMG_DS040485,"Venular Insufficiency, Systemic"
+BMGC_DS11921,BMG_DS040486,Stoll Alembik Dott syndrome
+BMGC_DS11922,BMG_DS040488,"Vasculopathy, Retinal, With Cerebral Leukodystrophy"
+BMGC_DS11923,BMG_DS040489,"Vasculitis, Lymphocytic, Nodular"
+BMGC_DS11924,BMG_DS040492,"Urticaria, Familial Localized Heat"
+BMGC_DS11925,BMG_DS040493,"Ureter, Bifid Or Double"
+BMGC_DS11926,BMG_DS040495,Upington disease
+BMGC_DS11927,BMG_DS040496,Undritz Anomaly
+BMGC_DS11928,BMG_DS040498,Ulna metaphyseal dysplasia syndrome
+BMGC_DS11929,BMG_DS040500,Tune Deafness
+BMGC_DS11930,BMG_DS040502,Tuberous Sclerosis 2
+BMGC_DS11931,BMG_DS040503,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7"
+BMGC_DS11932,BMG_DS040504,humerus trochlea aplasia
+BMGC_DS11933,BMG_DS040505,Tristichiasis
+BMGC_DS11934,BMG_DS040506,Transient Myeloproliferative Disorder of Down Syndrome
+BMGC_DS11935,BMG_DS040507,Triphalangeal thumbs brachyectrodactyly
+BMGC_DS11936,BMG_DS040508,Say Field Coldwell syndrome
+BMGC_DS11937,BMG_DS040509,Triphalangeal Thumb with Double Phalanges
+BMGC_DS11938,BMG_DS040510,Triosephosphate Isomerase Deficiency
+BMGC_DS11939,BMG_DS040511,"Triglyceride Storage Disease, Type II"
+BMGC_DS11940,BMG_DS040512,"Triglyceride Storage Disease, Type I"
+BMGC_DS11941,BMG_DS040514,"Trichorhinophalangeal Syndrome, Type III"
+BMGC_DS11942,BMG_DS040517,Familial multiple trichodiscomas
+BMGC_DS11943,BMG_DS040518,Neuhauser Daly Magnelli syndrome
+BMGC_DS11944,BMG_DS040519,"TREMOR, HEREDITARY ESSENTIAL, 1"
+BMGC_DS11945,BMG_DS040520,"Tremor of Intention, Ataxia, and Lipofuscinosis"
+BMGC_DS11946,BMG_DS040521,"colorectal cancer, hereditary nonpolyposis, type 6"
+BMGC_DS11947,BMG_DS040522,hereditary geniospasm
+BMGC_DS11948,BMG_DS040523,NOONAN SYNDROME 3
+BMGC_DS11949,BMG_DS040524,Esophageal atresia with or without tracheoesophageal fistula
+BMGC_DS11950,BMG_DS040526,"toes, space between first and second"
+BMGC_DS11951,BMG_DS040527,"toes, relative length of first and second"
+BMGC_DS11952,BMG_DS040528,"toe, rotated fifth"
+BMGC_DS11953,BMG_DS040529,"toe, misshapen"
+BMGC_DS11954,BMG_DS040530,"toe, fifth, number of phalanges 1N"
+BMGC_DS11955,BMG_DS040531,"tobacco addiction, susceptibility to"
+BMGC_DS11956,BMG_DS040532,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9"
+BMGC_DS11957,BMG_DS040533,"Tibial Torsion, Bilateral Medial"
+BMGC_DS11958,BMG_DS040534,"Tibia, Hypoplasia of, with Polydactyly"
+BMGC_DS11959,BMG_DS040535,Absence of tibia with polydactyly
+BMGC_DS11960,BMG_DS040536,THYROID HORMONE PLASMA MEMBRANE TRANSPORT DEFECT
+BMGC_DS11961,BMG_DS040537,Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency
+BMGC_DS11962,BMG_DS040541,"Thumbs, Stiff, With Brachydactyly Type A1 And Developmental Delay"
+BMGC_DS11963,BMG_DS040542,Thumb Deformity And Alopecia
+BMGC_DS11964,BMG_DS040543,Thrombophilia due to Activated Protein C Resistance
+BMGC_DS11965,BMG_DS040544,Venous Thromboembolism
+BMGC_DS11966,BMG_DS040545,Thrombocytopenia 2
+BMGC_DS11967,BMG_DS040546,"Thrombasthenia-Thrombocytopenia, Hereditary"
+BMGC_DS11968,BMG_DS040547,"Glanzmann Thrombasthenia, Autosomal Dominant"
+BMGC_DS11969,BMG_DS040549,Thoracolaryngopelvic dysplasia
+BMGC_DS11970,BMG_DS040550,"Thoracic Dysostosis, Isolated"
+BMGC_DS11971,BMG_DS040552,"Thalassemia, Beta+, Silent Allele"
+BMGC_DS11972,BMG_DS040553,tetramelic monodactyly
+BMGC_DS11973,BMG_DS040554,Tetralogy of fallot and glaucoma
+BMGC_DS11974,BMG_DS040555,Forebrain Defects
+BMGC_DS11975,BMG_DS040556,extensor tendons of finger anomalies
+BMGC_DS11976,BMG_DS040557,"ARTHROGRYPOSIS, DISTAL, TYPE 10"
+BMGC_DS11977,BMG_DS040559,"Teeth, Odd Shapes Of"
+BMGC_DS11978,BMG_DS040565,talonavicular coalition
+BMGC_DS11979,BMG_DS040566,Immunodeficiency due to Defect in CD3-Gamma
+BMGC_DS11980,BMG_DS040568,"syringomas, multiple"
+BMGC_DS11981,BMG_DS040569,"Granulomatous inflammatory arthritis, dermatitis and uveitis, familial"
+BMGC_DS11982,BMG_DS040570,"Synovial Chondromatosis, Familial, with Dwarfism"
+BMGC_DS11983,BMG_DS040571,TARSAL-CARPAL COALITION SYNDROME
+BMGC_DS11984,BMG_DS040573,"Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly"
+BMGC_DS11985,BMG_DS040575,Syndactyly-Polydactyly-Earlobe Syndrome
+BMGC_DS11986,BMG_DS040576,syndactyly type 5
+BMGC_DS11987,BMG_DS040577,"Syndactyly, Type IV"
+BMGC_DS11988,BMG_DS040578,"SYNDACTYLY, TYPE III"
+BMGC_DS11989,BMG_DS040580,"Syndactyly, Type I"
+BMGC_DS11990,BMG_DS040581,proximal symphalangism
+BMGC_DS11991,BMG_DS040583,distal symphalangism
+BMGC_DS11992,BMG_DS040584,"Symphalangism, C. S. Lewis Type"
+BMGC_DS11993,BMG_DS040586,Symphalangism of Toes
+BMGC_DS11994,BMG_DS040588,"Sulfhemoglobinemia, Congenital"
+BMGC_DS11995,BMG_DS040590,"Striae Distensae, Familial"
+BMGC_DS11996,BMG_DS040592,"strabismus, susceptibility to"
+BMGC_DS11997,BMG_DS040594,Stormorken Syndrome
+BMGC_DS11998,BMG_DS040596,Pseudohyperkalemia Cardiff
+BMGC_DS11999,BMG_DS040598,overhydrated hereditary stomatocytosis
+BMGC_DS12000,BMG_DS040599,Stiff Skin Syndrome
+BMGC_DS12001,BMG_DS040600,PROGRESSIVE ENCEPHALOMYELITIS WITH RIGIDITY
+BMGC_DS12002,BMG_DS040601,"Stickler syndrome, type 3"
+BMGC_DS12003,BMG_DS040603,COLCHICINE RESISTANCE
+BMGC_DS12004,BMG_DS040604,Cochleosaccular degeneration of the inner ear and progressive cataracts
+BMGC_DS12005,BMG_DS040605,"Cluster Headache, Familial"
+BMGC_DS12006,BMG_DS040606,Cleidorhizomelic syndrome
+BMGC_DS12007,BMG_DS040608,Blepharo-cheilo-dontic syndrome
+BMGC_DS12008,BMG_DS040609,OROFACIAL CLEFT 1
+BMGC_DS12009,BMG_DS040610,Split-Hand-Foot Malformation With Long Bone Deficiency 1
+BMGC_DS12010,BMG_DS040611,"Cirrhosis, Familial"
+BMGC_DS12011,BMG_DS040614,"Chylomicronemia, Familial, due to Circulating Inhibitor of Lipoprotein Lipase"
+BMGC_DS12012,BMG_DS040615,"Choreoathetosis, Familial Inverted"
+BMGC_DS12013,BMG_DS040622,Charcot-Marie-Tooth disease and deafness
+BMGC_DS12014,BMG_DS040624,"Charcot-Marie-Tooth Disease, Axonal, Type 2a1"
+BMGC_DS12015,BMG_DS040625,"Klippel-Feil syndrome 1, autosomal dominant"
+BMGC_DS12016,BMG_DS040626,Cervical Vertebral Dysplasia
+BMGC_DS12017,BMG_DS040627,cervical vertebral Bridge
+BMGC_DS12018,BMG_DS040628,Cervical Hypertrichosis with Underlying Kyphoscoliosis
+BMGC_DS12019,BMG_DS040629,"EAR WAX, WET/DRY"
+BMGC_DS12020,BMG_DS040631,Spinocerebellar Ataxia 29
+BMGC_DS12021,BMG_DS040632,"Dementia, familial Danish"
+BMGC_DS12022,BMG_DS040633,Spinocerebellar Ataxia 31
+BMGC_DS12023,BMG_DS040637,"Multiminicore Disease, Moderate, with Hand Involvement"
+BMGC_DS12024,BMG_DS040638,Median Arcuate Ligament Syndrome
+BMGC_DS12025,BMG_DS040639,Cavernous Malformations of CNS and Retina
+BMGC_DS12026,BMG_DS040640,Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated With Cerebral Capillary Malformations
+BMGC_DS12027,BMG_DS040642,"CATARACT, MARNER TYPE"
+BMGC_DS12028,BMG_DS040643,"CATARACT, POSTERIOR POLAR, 1"
+BMGC_DS12029,BMG_DS040645,"Cataract, Nuclear Diffuse Nonprogressive"
+BMGC_DS12030,BMG_DS040646,"Cataract, Zonular Pulverulent 1"
+BMGC_DS12031,BMG_DS040647,Cataract microcornea syndrome
+BMGC_DS12032,BMG_DS040650,"CATARACT, CONGENITAL, VOLKMANN TYPE"
+BMGC_DS12033,BMG_DS040652,carpal displacement
+BMGC_DS12034,BMG_DS040653,PARAGANGLIOMAS 4
+BMGC_DS12035,BMG_DS040655,"Cardiomyopathy, Familial Restrictive, 1"
+BMGC_DS12036,BMG_DS040656,hypertrophic cardiomyopathy 4
+BMGC_DS12037,BMG_DS040657,"Cardiomyopathy, Familial Hypertrophic, 3"
+BMGC_DS12038,BMG_DS040658,"Cardiomyopathy, Familial Hypertrophic, 2"
+BMGC_DS12039,BMG_DS040659,Familial Sudden Death
+BMGC_DS12040,BMG_DS040660,Monocyte Esterase Deficiency
+BMGC_DS12041,BMG_DS040662,Carabelli Anomaly of Maxillary Molar Teeth
+BMGC_DS12042,BMG_DS040663,Car Factor Deficiency
+BMGC_DS12043,BMG_DS040664,"CANINE TEETH, ABSENCE OF UPPER PERMANENT"
+BMGC_DS12044,BMG_DS040665,"cancer, familial, with in vitro Radioresistance"
+BMGC_DS12045,BMG_DS040666,CAMPOMELIC DYSPLASIA
+BMGC_DS12046,BMG_DS040667,Acampomelic Campomelic Dysplasia
+BMGC_DS12047,BMG_DS040668,camptobrachydactyly
+BMGC_DS12048,BMG_DS040669,"Callosities, Hereditary Painful"
+BMGC_DS12049,BMG_DS040670,"Idiopathic basal ganglia calcification, childhood onset"
+BMGC_DS12050,BMG_DS040671,"Calcific Aortic Disease with Immunologic Abnormalities, Familial"
+BMGC_DS12051,BMG_DS040672,"Cafe au lait spots, multiple"
+BMGC_DS12052,BMG_DS040675,"Heart Block, Nonprogressive"
+BMGC_DS12053,BMG_DS040676,"Cardiac Conduction Defect, Nonprogressive"
+BMGC_DS12054,BMG_DS040681,Brachymorphism-onychodysplasia-dysphalangism syndrome
+BMGC_DS12055,BMG_DS040685,Brachydactyly-Nystagmus-Cerebellar Ataxia
+BMGC_DS12056,BMG_DS040686,Fibular aplasia ectrodactyly
+BMGC_DS12057,BMG_DS040687,"Brachydactyly, Type E, with Atrial Septal Defect, Type II"
+BMGC_DS12058,BMG_DS040688,brachydactyly type E1
+BMGC_DS12059,BMG_DS040689,brachydactyly type C
+BMGC_DS12060,BMG_DS040690,brachydactyly type B1
+BMGC_DS12061,BMG_DS040691,Brachydactyly type A6
+BMGC_DS12062,BMG_DS040693,brachydactyly type A4
+BMGC_DS12063,BMG_DS040694,brachydactyly type A3
+BMGC_DS12064,BMG_DS040695,Brachydactyly type A1
+BMGC_DS12065,BMG_DS040696,Brachydactyly preaxial with hallux varus and thumb abduction
+BMGC_DS12066,BMG_DS040699,Brachydactyly with hypertension
+BMGC_DS12067,BMG_DS040700,"Brachmann-De Lange-Like Facial Changes With Microcephaly, Metatarsus Adductus, And Developmental Delay"
+BMGC_DS12068,BMG_DS040701,Weismann Netter syndrome
+BMGC_DS12069,BMG_DS040702,"bone pain, periodic"
+BMGC_DS12070,BMG_DS040703,Diaphyseal medullary stenosis with malignant fibrous histiocytoma
+BMGC_DS12071,BMG_DS040704,Cole Carpenter syndrome
+BMGC_DS12072,BMG_DS040708,Blepharoptosis myopia ectopia lentis
+BMGC_DS12073,BMG_DS040709,Bpes With Ovarian Failure
+BMGC_DS12074,BMG_DS040710,Bpes Without Ovarian Failure
+BMGC_DS12075,BMG_DS040711,Bpes With Duane Retraction Syndrome
+BMGC_DS12076,BMG_DS040712,"Blepharochalasis, Superior"
+BMGC_DS12077,BMG_DS040714,"Basilar Impression, Primary"
+BMGC_DS12078,BMG_DS040718,"Ovalocytosis, Malaysian-Melanesian-Filipino Type"
+BMGC_DS12079,BMG_DS040721,Axial osteomalacia
+BMGC_DS12080,BMG_DS040722,"Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities"
+BMGC_DS12081,BMG_DS040723,Aurocephalosyndactyly
+BMGC_DS12082,BMG_DS040724,Auriculoosteodysplasia
+BMGC_DS12083,BMG_DS040725,SVEINSSON CHORIORETINAL ATROPHY
+BMGC_DS12084,BMG_DS040726,Atrial Tachyarrhythmia with Short PR Interval
+BMGC_DS12085,BMG_DS040727,atrial septal defect 1
+BMGC_DS12086,BMG_DS040728,"Atrial Fibrillation, Familial, 4"
+BMGC_DS12087,BMG_DS040729,Ataxia with Fasciculations
+BMGC_DS12088,BMG_DS040730,"Ataxia, Spastic, with Congenital Miosis"
+BMGC_DS12089,BMG_DS040732,spermatogenic failure 2
+BMGC_DS12090,BMG_DS040735,Arthrogryposis-like hand anomaly and sensorineural deafness
+BMGC_DS12091,BMG_DS040736,Oculomelic amyoplasia
+BMGC_DS12092,BMG_DS040738,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 1"
+BMGC_DS12093,BMG_DS040740,"arms, malformation of"
+BMGC_DS12094,BMG_DS040748,"coronary artery disease, severe, susceptibility to"
+BMGC_DS12095,BMG_DS040749,Familial hypobetalipoproteinemia
+BMGC_DS12096,BMG_DS040750,"appendicitis, proneness to"
+BMGC_DS12097,BMG_DS040751,"Aortic Arch Interruption, Facial Palsy, and Retinal Coloboma"
+BMGC_DS12098,BMG_DS040752,Aortic arch anomaly with peculiar facies and mental retardation
+BMGC_DS12099,BMG_DS040753,Townes-Brocks-Branchiootorenal-Like Syndrome
+BMGC_DS12100,BMG_DS040754,anterior segment dysgenesis
+BMGC_DS12101,BMG_DS040756,Anonychia-onychodystrophy with hypoplasia or absence of distal phalanges
+BMGC_DS12102,BMG_DS040758,Anonychia-Ectrodactyly
+BMGC_DS12103,BMG_DS040759,Anonychia with Flexural Pigmentation
+BMGC_DS12104,BMG_DS040760,"spondyloarthropathy, susceptibility to, 1"
+BMGC_DS12105,BMG_DS040761,ankyloblepharon filiforme adnatum-cleft palate syndrome
+BMGC_DS12106,BMG_DS040762,"Aniridia, Microcornea, And Spontaneously Reabsorbed Cataract"
+BMGC_DS12107,BMG_DS040763,Aniridia and Absent Patella
+BMGC_DS12108,BMG_DS040764,Hereditary Angioedema Type II
+BMGC_DS12109,BMG_DS040767,"Aneurysm, Intracranial Berry, 1"
+BMGC_DS12110,BMG_DS040771,AMYOTROPHIC LATERAL SCLEROSIS 1
+BMGC_DS12111,BMG_DS040773,"Amyotrophic Lateral Sclerosis, Sporadic"
+BMGC_DS12112,BMG_DS040774,Amyotrophic Dystonic Paraplegia
+BMGC_DS12113,BMG_DS040776,"Amelogenesis Imperfecta, Type IV"
+BMGC_DS12114,BMG_DS040777,Amelia and Terminal Transverse Hemimelia
+BMGC_DS12115,BMG_DS040778,"Amastia, Bilateral, With Ureteral Triplication And Dysmorphism"
+BMGC_DS12116,BMG_DS040779,ALZHEIMER DISEASE 2
+BMGC_DS12117,BMG_DS040780,"ALZHEIMER DISEASE, FAMILIAL, 1"
+BMGC_DS12118,BMG_DS040782,alpha-Fetoprotein Deficiency
+BMGC_DS12119,BMG_DS040784,"Alopecia, Familial Focal"
+BMGC_DS12120,BMG_DS040785,Alopecia congenita keratosis palmoplantaris
+BMGC_DS12121,BMG_DS040786,ALOPECIA AREATA 1
+BMGC_DS12122,BMG_DS040787,Dysalbuminemic Hyperthyroxinemia
+BMGC_DS12123,BMG_DS040789,Hypoglossia-Hypodactylia
+BMGC_DS12124,BMG_DS040790,ADULT SYNDROME
+BMGC_DS12125,BMG_DS040791,"Adenosine Triphosphate, Elevated, Of Erythrocytes"
+BMGC_DS12126,BMG_DS040793,"Adenosine Deaminase, Elevated, Hemolytic Anemia Due To"
+BMGC_DS12127,BMG_DS040794,"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
+BMGC_DS12129,BMG_DS040796,"Acropectorovertebral Dysplasia, F-Form"
+BMGC_DS12130,BMG_DS040797,"Acroleukopathy, Symmetric"
+BMGC_DS12131,BMG_DS040798,"Acrokeratoderma, Hereditary Papulotranslucent"
+BMGC_DS12132,BMG_DS040799,Saethre-Chotzen Syndrome with Eyelid Anomalies
+BMGC_DS12133,BMG_DS040800,Apert-Crouzon Disease
+BMGC_DS12134,BMG_DS040802,Autosomal dominant compelling helio ophthalmic outburst syndrome
+BMGC_DS12135,BMG_DS040803,"HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE"
+BMGC_DS12136,BMG_DS040807,Stargardt disease 4
+BMGC_DS12137,BMG_DS040808,"HYPERCHOLESTEROLEMIA, FAMILIAL, 3"
+BMGC_DS12138,BMG_DS040810,Young Simpson syndrome
+BMGC_DS12139,BMG_DS040811,"Deafness, Autosomal Recessive 16"
+BMGC_DS12140,BMG_DS040813,Hereditary Myopathy with Early Respiratory Failure
+BMGC_DS12141,BMG_DS040814,prostate cancer/brain cancer susceptibility
+BMGC_DS12142,BMG_DS040815,"DEAFNESS, AUTOSOMAL RECESSIVE 14"
+BMGC_DS12143,BMG_DS040816,ACROMELIC FRONTONASAL DYSOSTOSIS
+BMGC_DS12144,BMG_DS040822,Cone-Rod Dystrophy 7
+BMGC_DS12145,BMG_DS040826,"Deafness, Autosomal Recessive 21"
+BMGC_DS12146,BMG_DS040827,"DEAFNESS, AUTOSOMAL DOMINANT 17"
+BMGC_DS12147,BMG_DS040829,Craniosynostosis with Ectopia Lentis
+BMGC_DS12148,BMG_DS040830,"Xanthinuria, Type II"
+BMGC_DS12149,BMG_DS040834,"Spastic paraplegia 8, autosomal dominant"
+BMGC_DS12150,BMG_DS040835,"HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2"
+BMGC_DS12151,BMG_DS040836,"Hemophagocytic lymphohistiocytosis, familial, 4"
+BMGC_DS12152,BMG_DS040837,Spondyloepimetaphyseal dysplasia with multiple dislocations
+BMGC_DS12153,BMG_DS040838,enlarged vestibular aqueduct syndrome
+BMGC_DS12154,BMG_DS040839,LIMB-MAMMARY SYNDROME
+BMGC_DS12155,BMG_DS040842,"Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema"
+BMGC_DS12156,BMG_DS040843,Neuronal intranuclear inclusion disease
+BMGC_DS12157,BMG_DS040844,Adult-onset citrullinemia type 2
+BMGC_DS12158,BMG_DS040846,Coloboma of superior eyelid
+BMGC_DS12159,BMG_DS040847,"Arhinia, choanal atresia, and microphthalmia"
+BMGC_DS12160,BMG_DS040850,radioulnar synostosis-microcephaly-scoliosis syndrome
+BMGC_DS12161,BMG_DS040857,Megalancephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome
+BMGC_DS12162,BMG_DS040859,"Glaucoma 1, Open Angle, F"
+BMGC_DS12163,BMG_DS040860,"long chain fatty acids, defect in transport of"
+BMGC_DS12164,BMG_DS040861,"Hyperthyroidism, Familial Gestational"
+BMGC_DS12165,BMG_DS040864,Finnish lethal neonatal metabolic syndrome
+BMGC_DS12166,BMG_DS040865,SCHIZOPHRENIA 2
+BMGC_DS12167,BMG_DS040867,Cerebral Cavernous Malformations 3
+BMGC_DS12168,BMG_DS040868,CEREBRAL CAVERNOUS MALFORMATIONS 2
+BMGC_DS12169,BMG_DS040869,"DIABETES MELLITUS, INSULIN-DEPENDENT, 17"
+BMGC_DS12170,BMG_DS040870,"PSEUDOHYPOPARATHYROIDISM, TYPE IB"
+BMGC_DS12171,BMG_DS040871,Myopia 3
+BMGC_DS12172,BMG_DS040872,HUNTINGTON DISEASE-LIKE 1
+BMGC_DS12173,BMG_DS040874,"Epilepsy, Nocturnal Frontal Lobe, Type 2"
+BMGC_DS12174,BMG_DS040875,"MECKEL SYNDROME, TYPE 2"
+BMGC_DS12175,BMG_DS040878,"Dermatitis, Atopic, 1"
+BMGC_DS12176,BMG_DS040884,CDAGS SYNDROME
+BMGC_DS12177,BMG_DS040885,"DEAFNESS, AUTOSOMAL RECESSIVE 13"
+BMGC_DS12178,BMG_DS040886,"Macular Degeneration, Age-Related, 1"
+BMGC_DS12179,BMG_DS040888,Endplate Acetylcholinesterase Deficiency
+BMGC_DS12180,BMG_DS040890,SCHIZOPHRENIA 6
+BMGC_DS12181,BMG_DS040891,"Deafness, Autosomal Recessive 17"
+BMGC_DS12182,BMG_DS040893,"ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE"
+BMGC_DS12183,BMG_DS040894,PREMATURE CHROMATID SEPARATION TRAIT
+BMGC_DS12184,BMG_DS040895,"Peroxisome Biogenesis Disorder, Complementation Group 7"
+BMGC_DS12185,BMG_DS040896,Muenke Syndrome
+BMGC_DS12186,BMG_DS040897,Histiocytosis with joint contractures and sensorineural deafness
+BMGC_DS12187,BMG_DS040898,Retinitis Pigmentosa 25
+BMGC_DS12188,BMG_DS040900,PSORIASIS 2
+BMGC_DS12189,BMG_DS040901,autosomal recessive distal renal tubular acidosis
+BMGC_DS12190,BMG_DS040904,"Cataract, posterior polar, 4"
+BMGC_DS12191,BMG_DS040905,RETINITIS PIGMENTOSA 36
+BMGC_DS12192,BMG_DS040906,"Diabetes Mellitus, Transient Neonatal, 3"
+BMGC_DS12193,BMG_DS040907,"CHROMOSOME 16p13.3 DELETION SYNDROME, PROXIMAL"
+BMGC_DS12194,BMG_DS040909,"GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY"
+BMGC_DS12195,BMG_DS040910,"Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate"
+BMGC_DS12196,BMG_DS040911,"Glaucoma 1, Open Angle, M"
+BMGC_DS12197,BMG_DS040912,hypomyelinating leukodystrophy 5
+BMGC_DS12198,BMG_DS040913,"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4"
+BMGC_DS12199,BMG_DS040914,NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCY
+BMGC_DS12200,BMG_DS040915,"Neuronal Ceroid Lipofuscinosis, Congenital"
+BMGC_DS12201,BMG_DS040916,"Microphthalmia, Syndromic 6"
+BMGC_DS12202,BMG_DS040917,"Microphthalmia, Syndromic 5"
+BMGC_DS12203,BMG_DS040918,Complement Component 7 Deficiency
+BMGC_DS12204,BMG_DS040919,"Giant Axonal Neuropathy, Autosomal Dominant"
+BMGC_DS12205,BMG_DS040920,"Myopathy, Distal 3"
+BMGC_DS12206,BMG_DS040921,"MICROPHTHALMIA, ISOLATED 2"
+BMGC_DS12207,BMG_DS040922,"Microphthalmia, Isolated, with Coloboma 3"
+BMGC_DS12208,BMG_DS040923,"Microphthalmia, Cataracts, and Iris Abnormalities"
+BMGC_DS12209,BMG_DS040924,Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency
+BMGC_DS12210,BMG_DS040926,"Polyposis Syndrome, Hereditary Mixed, 2"
+BMGC_DS12211,BMG_DS040929,"opioid dependence, susceptibility to, 1"
+BMGC_DS12212,BMG_DS040930,"Corneal Dystrophy, Congenital Stromal"
+BMGC_DS12213,BMG_DS040931,"Deafness, Autosomal Recessive 53"
+BMGC_DS12214,BMG_DS040935,Short Stature And Facioauriculothoracic Malformations
+BMGC_DS12215,BMG_DS040936,TRICHILEMMAL CYST 1
+BMGC_DS12216,BMG_DS040937,"Deafness, Autosomal Recessive 46"
+BMGC_DS12217,BMG_DS040938,"Deafness, Autosomal Recessive 42"
+BMGC_DS12218,BMG_DS040940,Frias syndrome
+BMGC_DS12219,BMG_DS040941,"Epidermolysis bullosa, lethal acantholytic"
+BMGC_DS12220,BMG_DS040942,HOLOPROSENCEPHALY 5
+BMGC_DS12221,BMG_DS040943,ALZHEIMER DISEASE 10
+BMGC_DS12222,BMG_DS040944,maturity-onset diabetes of the young type 7
+BMGC_DS12223,BMG_DS040945,Combined Oxidative Phosphorylation Deficiency 3
+BMGC_DS12224,BMG_DS040946,Combined Oxidative Phosphorylation Deficiency 2
+BMGC_DS12225,BMG_DS040947,"Pigmented Nodular Adrenocortical Disease, Primary, 1"
+BMGC_DS12226,BMG_DS040949,RETINAL CONE DYSTROPHY 4
+BMGC_DS12227,BMG_DS040950,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 11"
+BMGC_DS12228,BMG_DS040951,"Pigmented Nodular Adrenocortical Disease, Primary, 2"
+BMGC_DS12229,BMG_DS040952,CATSHL syndrome
+BMGC_DS12230,BMG_DS040953,"Tumoral Calcinosis, Normophosphatemic, Familial"
+BMGC_DS12231,BMG_DS040954,"Buruli ulcer, susceptibility to"
+BMGC_DS12232,BMG_DS040955,"Night Blindness, Congenital Stationary, Autosomal Dominant 1"
+BMGC_DS12233,BMG_DS040956,"Night Blindness, Congenital Stationary, Autosomal Dominant 3"
+BMGC_DS12234,BMG_DS040957,Chromosome 17q21.31 Deletion Syndrome
+BMGC_DS12235,BMG_DS040958,"Spondyloepimetaphyseal dysplasia, Genevieve type"
+BMGC_DS12236,BMG_DS040959,Testicular Microlithiasis
+BMGC_DS12237,BMG_DS040963,"Night Blindness, Congenital Stationary, Type 2B"
+BMGC_DS12238,BMG_DS040966,"hepatitis B virus, susceptibility to"
+BMGC_DS12239,BMG_DS040967,Retinal Cone Dystrophy 3A
+BMGC_DS12240,BMG_DS040968,"Brachydactyly, Coloboma, And Anterior Segment Dysgenesis"
+BMGC_DS12241,BMG_DS040969,"Hyperinsulinemic hypoglycemia, familial, 7"
+BMGC_DS12242,BMG_DS040970,Hyperinsulinemic hypoglycemia
+BMGC_DS12243,BMG_DS040971,"Cataract, autosomal recessive congenital 2"
+BMGC_DS12244,BMG_DS040972,"Glutamine deficiency, congenital"
+BMGC_DS12245,BMG_DS040973,2-Methylbutyryl-CoA Dehydrogenase Deficiency
+BMGC_DS12246,BMG_DS040974,Northern epilepsy syndrome
+BMGC_DS12247,BMG_DS040979,Osteosclerosis with ichthyosis and premature ovarian failure
+BMGC_DS12248,BMG_DS040983,"Natural Killer Cell Deficiency, Familial Isolated"
+BMGC_DS12249,BMG_DS040984,"Hyperinsulinemic Hypoglycemia, Familial, 4"
+BMGC_DS12250,BMG_DS040985,"Hyperinsulinemic Hypoglycemia, Familial, 5"
+BMGC_DS12251,BMG_DS040986,"Deafness, Autosomal Dominant 53"
+BMGC_DS12252,BMG_DS040990,"DEAFNESS, AUTOSOMAL RECESSIVE 55"
+BMGC_DS12253,BMG_DS040991,"Deafness, Autosomal Recessive 47"
+BMGC_DS12254,BMG_DS040992,"Brachyphalangy, polydactyly, and tibial aplasia-hypoplasia"
+BMGC_DS12255,BMG_DS040993,"Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features"
+BMGC_DS12256,BMG_DS040994,"DEAFNESS, AUTOSOMAL RECESSIVE 51"
+BMGC_DS12257,BMG_DS040996,"Migraine, Familial Hemiplegic, 3"
+BMGC_DS12258,BMG_DS040999,"Visceral Neuropathy, Familial, Autosomal Dominant"
+BMGC_DS12259,BMG_DS041000,Majeed syndrome
+BMGC_DS12260,BMG_DS041001,Short QT Syndrome 3
+BMGC_DS12261,BMG_DS041002,Short QT Syndrome 2
+BMGC_DS12262,BMG_DS041003,Short QT Syndrome 1
+BMGC_DS12263,BMG_DS041004,"Spondylomegaepiphyseal Dysplasia With Upper Limb Mesomelia, Punctate Calcifications, And Deafness"
+BMGC_DS12264,BMG_DS041005,"fibrosis of extraocular muscles, congenital, with synergistic divergence"
+BMGC_DS12265,BMG_DS041007,PARIETAL FORAMINA 2
+BMGC_DS12266,BMG_DS041008,"SCAPHOCEPHALY, MAXILLARY RETRUSION, AND IMPAIRED INTELLECTUAL DEVELOPMENT"
+BMGC_DS12267,BMG_DS041010,"Tooth Agenesis, Selective, 2"
+BMGC_DS12268,BMG_DS041011,"Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal"
+BMGC_DS12269,BMG_DS041015,BRANCHIOOTIC SYNDROME 1
+BMGC_DS12270,BMG_DS041016,Congenital disorder of glycosylation type 1B
+BMGC_DS12271,BMG_DS041018,Mandibulofacial Dysostosis with Macroblepharon and Macrostomia
+BMGC_DS12272,BMG_DS041021,"Spondyloepimetaphyseal Dysplasia, Shohat Type"
+BMGC_DS12273,BMG_DS041024,Torsion dystonia with onset in infancy
+BMGC_DS12274,BMG_DS041027,"Muscular Dystrophy, Congenital, Megaconial Type"
+BMGC_DS12275,BMG_DS041028,"ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS"
+BMGC_DS12276,BMG_DS041029,"Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly"
+BMGC_DS12277,BMG_DS041030,Bartter disease type 4A
+BMGC_DS12278,BMG_DS041032,Megalencephaly cutis marmorata telangiectatica congenita
+BMGC_DS12279,BMG_DS041033,"MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA"
+BMGC_DS12280,BMG_DS041034,"HYPERLIPIDEMIA, COMBINED, 1"
+BMGC_DS12281,BMG_DS041035,"Hyperinsulinemic hypoglycemia, familial, 3"
+BMGC_DS12282,BMG_DS041037,Pelvic dysplasia arthrogryposis of lower limbs
+BMGC_DS12283,BMG_DS041038,Auriculo-condylar syndrome
+BMGC_DS12284,BMG_DS041039,"MIGRAINE, FAMILIAL HEMIPLEGIC, 2"
+BMGC_DS12285,BMG_DS041040,"Migraine, Familial Basilar"
+BMGC_DS12286,BMG_DS041041,"Febrile Convulsions, Familial, 2"
+BMGC_DS12287,BMG_DS041042,OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE
+BMGC_DS12288,BMG_DS041043,Ethylmalonic encephalopathy
+BMGC_DS12289,BMG_DS041045,short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome
+BMGC_DS12290,BMG_DS041046,"Deafness, Autosomal Dominant 15"
+BMGC_DS12291,BMG_DS041047,Severe combined immunodeficiency with sensitivity to ionizing radiation
+BMGC_DS12292,BMG_DS041048,"SEVERE COMBINED IMMUNODEFICIENCY, ATHABASKAN-TYPE"
+BMGC_DS12293,BMG_DS041049,"SEVERE COMBINED IMMUNODEFICIENCY, PARTIAL"
+BMGC_DS12294,BMG_DS041050,"Amyotrophy, monomelic"
+BMGC_DS12295,BMG_DS041051,"Amyotrophic Lateral Sclerosis 4, Juvenile"
+BMGC_DS12296,BMG_DS041053,congenital bilateral absence of vas deferens
+BMGC_DS12297,BMG_DS041054,Weyers ulnar ray-oligodactyly syndrome
+BMGC_DS12298,BMG_DS041057,Desmosterolosis
+BMGC_DS12299,BMG_DS041058,"HEMOCHROMATOSIS, TYPE 2A"
+BMGC_DS12300,BMG_DS041059,"HEMOCHROMATOSIS, TYPE 2B"
+BMGC_DS12301,BMG_DS041060,Gracile bone dysplasia
+BMGC_DS12302,BMG_DS041061,"Cholestasis, progressive familial intrahepatic 3"
+BMGC_DS12303,BMG_DS041062,"Plantar Lipomatosis, Unusual Facies, and Developmental Delay"
+BMGC_DS12304,BMG_DS041064,"Spondylometaphyseal dysplasia, axial"
+BMGC_DS12305,BMG_DS041067,"XANTHOMATOSIS, SUSCEPTIBILITY TO"
+BMGC_DS12306,BMG_DS041068,Ventriculomegaly With Defects Of The Radius And Kidney
+BMGC_DS12307,BMG_DS041069,Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency
+BMGC_DS12308,BMG_DS041070,Pierre Robin sequence with pectus excavatum and rib and scapular anomalies
+BMGC_DS12309,BMG_DS041071,RHYNS syndrome
+BMGC_DS12310,BMG_DS041074,"TREMOR, HEREDITARY ESSENTIAL, 2"
+BMGC_DS12311,BMG_DS041075,Torsion dystonia 7
+BMGC_DS12312,BMG_DS041076,"CERVICAL DYSTONIA, PRIMARY"
+BMGC_DS12313,BMG_DS041077,"Nephropathy, Progressive Tubulointerstitial, with Cholestatic Liver Disease"
+BMGC_DS12314,BMG_DS041078,"Spondyloepimetaphyseal Dysplasia, Missouri Type"
+BMGC_DS12315,BMG_DS041080,amyotrophic lateral sclerosis type 5
+BMGC_DS12316,BMG_DS041081,"Usher Syndrome, Type IE"
+BMGC_DS12317,BMG_DS041082,Congenital sensorineural hearing loss
+BMGC_DS12318,BMG_DS041083,ALZHEIMER DISEASE 5
+BMGC_DS12319,BMG_DS041084,Cone Dystrophy 3
+BMGC_DS12320,BMG_DS041085,"Deafness, Autosomal Recessive 18"
+BMGC_DS12321,BMG_DS041086,"HEMANGIOMA, CAPILLARY INFANTILE"
+BMGC_DS12322,BMG_DS041087,NEPHRONOPHTHISIS 2
+BMGC_DS12323,BMG_DS041088,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 4"
+BMGC_DS12324,BMG_DS041089,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 3"
+BMGC_DS12325,BMG_DS041090,"Polydactyly, Postaxial, Type A2"
+BMGC_DS12326,BMG_DS041091,"Usher Syndrome, Type IF"
+BMGC_DS12327,BMG_DS041092,"FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2"
+BMGC_DS12328,BMG_DS041093,Bilateral ptosis
+BMGC_DS12329,BMG_DS041094,"Broad Terminal Phalanges, Familial"
+BMGC_DS12330,BMG_DS041095,"Infantile convulsions and paroxysmal choreoathetosis, familial"
+BMGC_DS12331,BMG_DS041096,pure hair and nail ectodermal dysplasia
+BMGC_DS12332,BMG_DS041097,"Hypomagnesemia 1, Intestinal"
+BMGC_DS12333,BMG_DS041098,FRIEDREICH ATAXIA 2
+BMGC_DS12334,BMG_DS041099,Hyperzincemia with Functional Zinc Depletion
+BMGC_DS12335,BMG_DS041101,Odontotrichoungual-Digital-Palmar Syndrome
+BMGC_DS12336,BMG_DS041102,"Muscular Dystrophy, Limb-Girdle, Type 2G"
+BMGC_DS12337,BMG_DS041103,Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma
+BMGC_DS12338,BMG_DS041104,"EPISODIC ATAXIA, TYPE 5"
+BMGC_DS12339,BMG_DS041105,"DIABETES MELLITUS, INSULIN-DEPENDENT, 10"
+BMGC_DS12340,BMG_DS041106,"DIABETES MELLITUS, INSULIN-DEPENDENT, 6"
+BMGC_DS12341,BMG_DS041107,Severe hydrops
+BMGC_DS12342,BMG_DS041108,"Deafness, Congenital Heart Defects, and Posterior Embryotoxon"
+BMGC_DS12343,BMG_DS041109,orofacial cleft 10
+BMGC_DS12344,BMG_DS041110,glomerulopathy with fibronectin deposits 2
+BMGC_DS12345,BMG_DS041112,"malignant hyperthermia, susceptibility to, 5"
+BMGC_DS12346,BMG_DS041113,"Cataract, Zonular Pulverulent 3"
+BMGC_DS12347,BMG_DS041114,Left-Right Axis Malformations
+BMGC_DS12348,BMG_DS041115,"DEAFNESS, AUTOSOMAL RECESSIVE 15"
+BMGC_DS12349,BMG_DS041116,"Deafness, Autosomal Dominant 13"
+BMGC_DS12350,BMG_DS041117,"Autoimmune Lymphoproliferative Syndrome, Type IA"
+BMGC_DS12351,BMG_DS041118,"Autoimmune Lymphoproliferative Syndrome, Type IB"
+BMGC_DS12352,BMG_DS041121,Vacuolar Neuromyopathy
+BMGC_DS12353,BMG_DS041123,Phosphoglycerate Dehydrogenase Deficiency
+BMGC_DS12354,BMG_DS041124,Exudative Vitreoretinopathy 4
+BMGC_DS12355,BMG_DS041125,Penttinen-Aula syndrome
+BMGC_DS12356,BMG_DS041126,"Premature Aging Syndrome, Okamoto Type"
+BMGC_DS12357,BMG_DS041127,Spondylospinal Thoracic Dysostosis
+BMGC_DS12358,BMG_DS041128,Coloboma-Obesity-Hypogenitalism-Mental Retardation Syndrome
+BMGC_DS12359,BMG_DS041129,"Peroxisome Biogenesis Disorder, Complementation Group K"
+BMGC_DS12360,BMG_DS041132,Retinal cone dystrophy 2
+BMGC_DS12361,BMG_DS041133,"Ehlers-Danlos syndrome, musculocontractural type"
+BMGC_DS12362,BMG_DS041134,Preaxial Hallucal Polydactyly
+BMGC_DS12363,BMG_DS041138,"systemic lupus erythematosus, susceptibility to, 1"
+BMGC_DS12364,BMG_DS041139,Proteus-Like Syndrome
+BMGC_DS12365,BMG_DS041140,RETINITIS PIGMENTOSA 19
+BMGC_DS12366,BMG_DS041141,Quebec platelet disorder
+BMGC_DS12367,BMG_DS041142,"Superior Transverse Scapular Ligament, Calcification Of, Familial"
+BMGC_DS12368,BMG_DS041143,Yemenite deaf-blind hypopigmentation syndrome
+BMGC_DS12369,BMG_DS041144,"T-cell immunodeficiency, congenital alopecia and nail dystrophy"
+BMGC_DS12370,BMG_DS041145,Arthrogryposis and ectodermal dysplasia
+BMGC_DS12371,BMG_DS041146,"Sebaceous gland hyperplasia, familial presenile"
+BMGC_DS12372,BMG_DS041148,glaucoma type 1C
+BMGC_DS12373,BMG_DS041149,"Bartter syndrome, antenatal type 1"
+BMGC_DS12374,BMG_DS041151,Photosensitive Trichothiodystrophy
+BMGC_DS12375,BMG_DS041154,"DIABETES MELLITUS, INSULIN-DEPENDENT, 15"
+BMGC_DS12376,BMG_DS041155,Paragangliomas 2
+BMGC_DS12377,BMG_DS041156,"Neural tube defect, folate-sensitive"
+BMGC_DS12378,BMG_DS041158,"Iridogoniodysgenesis, Type 1"
+BMGC_DS12379,BMG_DS041160,Iris Pigment Epithelium Anomalies
+BMGC_DS12380,BMG_DS041161,Spastic Paraplegia And Evans Syndrome
+BMGC_DS12381,BMG_DS041163,"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C"
+BMGC_DS12382,BMG_DS041164,Steinfeld Syndrome
+BMGC_DS12383,BMG_DS041165,Steatocystoma multiplex with natal teeth
+BMGC_DS12384,BMG_DS041166,Stapes ankylosis with broad thumb and toe syndrome
+BMGC_DS12385,BMG_DS041167,"Spondylometaphyseal dysplasia, Algerian type"
+BMGC_DS12386,BMG_DS041168,"Spondyloepiphyseal Dysplasia Tarda, Autosomal Dominant"
+BMGC_DS12387,BMG_DS041172,"SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 2"
+BMGC_DS12388,BMG_DS041174,"SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS"
+BMGC_DS12389,BMG_DS041175,Split-Hand And Split-Foot With Hypodontia
+BMGC_DS12390,BMG_DS041176,split lower lip
+BMGC_DS12391,BMG_DS041178,Splenogonadal fusion limb defects micrognatia
+BMGC_DS12392,BMG_DS041179,Spinocerebellar Atrophy With Pupillary Paralysis
+BMGC_DS12393,BMG_DS041181,Spinocerebellar Ataxia With Rigidity And Peripheral Neuropathy
+BMGC_DS12394,BMG_DS041182,"spinal muscular atrophy, segmental"
+BMGC_DS12395,BMG_DS041184,"Spinal Muscular Atrophy, Facioscapulohumeral Type"
+BMGC_DS12396,BMG_DS041185,"Neuronopathy, Distal Hereditary Motor, Type I"
+BMGC_DS12397,BMG_DS041186,Spheroid body myopathy
+BMGC_DS12398,BMG_DS041188,"Speech Development, Delayed, With Facial Asymmetry, Strabismus, And Transverse Earlobe Crease"
+BMGC_DS12399,BMG_DS041189,ELLIPTOCYTOSIS 3
+BMGC_DS12400,BMG_DS041190,"Spastic Paraplegia, Optic Atrophy, And Dementia"
+BMGC_DS12401,BMG_DS041192,Spastic paraplegia neuropathy poikiloderma
+BMGC_DS12402,BMG_DS041193,Spastic Paraplegia With Associated Extrapyramidal Signs
+BMGC_DS12403,BMG_DS041194,"Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, And Progressive Nephropathy"
+BMGC_DS12404,BMG_DS041196,"Spastic paraplegia 4, autosomal dominant"
+BMGC_DS12405,BMG_DS041198,Skeletal Dysplasia With Delayed Epiphyseal And Carpal Bone Ossification
+BMGC_DS12406,BMG_DS041200,Shprintzen omphalocele syndrome
+BMGC_DS12407,BMG_DS041201,"sella turcica, bridged"
+BMGC_DS12408,BMG_DS041202,Sinus Node Disease and Myopia
+BMGC_DS12409,BMG_DS041203,Simosa cranio facial syndrome
+BMGC_DS12410,BMG_DS041204,"SCLERODERMA, FAMILIAL PROGRESSIVE"
+BMGC_DS12411,BMG_DS041206,Scholte syndrome
+BMGC_DS12412,BMG_DS041208,Ulnar-mammary syndrome
+BMGC_DS12413,BMG_DS041209,"Scapuloperoneal Syndrome, Neurogenic, Kaeser Type"
+BMGC_DS12414,BMG_DS041210,SCALP-EAR-NIPPLE SYNDROME
+BMGC_DS12415,BMG_DS041211,Scalp defects postaxial polydactyly
+BMGC_DS12416,BMG_DS041212,Say syndrome
+BMGC_DS12417,BMG_DS041218,Robinow Sorauf syndrome
+BMGC_DS12418,BMG_DS041219,Rombo syndrome
+BMGC_DS12419,BMG_DS041220,RING DERMOID OF CORNEA
+BMGC_DS12420,BMG_DS041221,rhiny
+BMGC_DS12421,BMG_DS041222,"rhabdomyosarcoma, embryonal, 2"
+BMGC_DS12422,BMG_DS041225,"Retinopathy, Pericentral Pigmentary, Dominant"
+BMGC_DS12423,BMG_DS041226,Retinitis Pigmentosa 10
+BMGC_DS12424,BMG_DS041227,RETINITIS PIGMENTOSA 9
+BMGC_DS12425,BMG_DS041229,RETINAL CONE DYSTROPHY 1
+BMGC_DS12426,BMG_DS041231,Reticular Dystrophy Of Retinal Pigment Epithelium
+BMGC_DS12427,BMG_DS041232,Red cell phospholipid defect with hemolysis
+BMGC_DS12428,BMG_DS041234,raindrop hypopigmentation
+BMGC_DS12429,BMG_DS041236,"RADIUS, APLASIA OF, WITH CLEFT LIP/PALATE"
+BMGC_DS12430,BMG_DS041237,RADIAL-RENAL SYNDROME
+BMGC_DS12431,BMG_DS041238,"Radial hypoplasia, triphalangeal thumbs and hypospadias"
+BMGC_DS12432,BMG_DS041239,"Radial Heads, Posterior Dislocation Of"
+BMGC_DS12433,BMG_DS041240,Infantile Hypertrophic Pyloric Stenosis
+BMGC_DS12434,BMG_DS041241,PULMONIC STENOSIS AND DEAFNESS
+BMGC_DS12435,BMG_DS041242,Ciuffo Syndrome
+BMGC_DS12436,BMG_DS041244,Pubic Bone Dysplasia
+BMGC_DS12437,BMG_DS041245,"Ptosis, Strabismus, And Ectopic Pupils"
+BMGC_DS12438,BMG_DS041246,"Ptosis, Hereditary Congenital 1"
+BMGC_DS12439,BMG_DS041247,"Pterygium, Antecubital"
+BMGC_DS12440,BMG_DS041248,Autosomal dominant multiple pterygium syndrome
+BMGC_DS12441,BMG_DS041249,"Pterygium Colli, Isolated"
+BMGC_DS12442,BMG_DS041250,Haspeslagh Fryns Muelenaere syndrome
+BMGC_DS12443,BMG_DS041251,"psoriasis 1, susceptibility to"
+BMGC_DS12444,BMG_DS041252,"Pseudoxanthoma Elasticum, Incomplete"
+BMGC_DS12445,BMG_DS041256,"Butyrylcholinesterase Deficiency, Fluoride-Resistant, Japanese Type"
+BMGC_DS12446,BMG_DS041259,"Pruritus, Hereditary Localized"
+BMGC_DS12447,BMG_DS041262,benign neoplasm of eye
+BMGC_DS12448,BMG_DS041265,Premature coronary artery disease
+BMGC_DS12449,BMG_DS041266,Primary Release Disorder Of Platelets
+BMGC_DS12450,BMG_DS041268,"Presenile dementia, Kraepelin type"
+BMGC_DS12451,BMG_DS041271,"Preaxial deficiency, postaxial polydactyly and hypospadias"
+BMGC_DS12452,BMG_DS041273,LONG QT SYNDROME 5
+BMGC_DS12453,BMG_DS041274,Posterior column ataxia
+BMGC_DS12454,BMG_DS041275,postaxial tetramelic oligodactyly
+BMGC_DS12455,BMG_DS041276,"Porphyria Cutanea Tarda, Type I"
+BMGC_DS12456,BMG_DS041277,"Porphyria, Acute Intermittent, Nonerythroid Variant"
+BMGC_DS12457,BMG_DS041278,"POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC, 1"
+BMGC_DS12458,BMG_DS041279,punctate palmoplantar keratoderma type 2
+BMGC_DS12459,BMG_DS041280,Familial porencephaly
+BMGC_DS12460,BMG_DS041283,polyposis of gastric fundus without polyposis coli
+BMGC_DS12461,BMG_DS041284,"polyposis, intestinal, with multiple exostoses"
+BMGC_DS12462,BMG_DS041285,"polyposis, intestinal, scattered and discrete"
+BMGC_DS12463,BMG_DS041288,Juvenile Polyposis Coli
+BMGC_DS12464,BMG_DS041290,polysyndactyly 4
+BMGC_DS12465,BMG_DS041292,"Polydactyly, Preaxial III"
+BMGC_DS12466,BMG_DS041293,polydactyly of a triphalangeal thumb
+BMGC_DS12467,BMG_DS041294,"POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA"
+BMGC_DS12468,BMG_DS041295,Orofaciodigital syndrome 5
+BMGC_DS12469,BMG_DS041296,postaxial polydactyly type B
+BMGC_DS12470,BMG_DS041297,Medullary cystic kidney disease 1
+BMGC_DS12471,BMG_DS041300,"PNEUMOTHORAX, PRIMARY SPONTANEOUS"
+BMGC_DS12472,BMG_DS041301,Platelet Signal Processing Defect
+BMGC_DS12473,BMG_DS041305,Platelet Factor 3 Deficiency
+BMGC_DS12474,BMG_DS041306,"Platelet Disorder, Undefined"
+BMGC_DS12475,BMG_DS041309,Robin sequence and oligodactyly
+BMGC_DS12476,BMG_DS041310,Pigmented Paravenous Chorioretinal Atrophy
+BMGC_DS12477,BMG_DS041311,Telfer Sugar Jaeger syndrome
+BMGC_DS12478,BMG_DS041313,6-Phosphogluconolactonase Deficiency
+BMGC_DS12479,BMG_DS041316,Phlebectasia Of Lips
+BMGC_DS12480,BMG_DS041317,pheochromocytoma-islet cell tumor syndrome
+BMGC_DS12481,BMG_DS041320,Accessory deep peroneal nerve
+BMGC_DS12482,BMG_DS041321,"Normokalemic Periodic Paralysis, Potassium-Sensitive"
+BMGC_DS12483,BMG_DS041325,Pelvis-Shoulder Dysplasia
+BMGC_DS12484,BMG_DS041326,Pelvic Lipomatosis with Crossed Renal Ectopia
+BMGC_DS12485,BMG_DS041327,"Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant"
+BMGC_DS12486,BMG_DS041328,Pechet Factor Deficiency
+BMGC_DS12487,BMG_DS041330,Patterned dystrophy of retinal pigment epithelium
+BMGC_DS12488,BMG_DS041331,CHAR SYNDROME
+BMGC_DS12489,BMG_DS041333,"Paroxysmal Tonic Upgaze, Benign Childhood, With Ataxia"
+BMGC_DS12490,BMG_DS041334,patella aplasia/hypoplasia
+BMGC_DS12491,BMG_DS041335,"Patella aplasia, coxa vara, tarsal synostosis"
+BMGC_DS12492,BMG_DS041336,"Parotidomegaly, Hereditary Bilateral"
+BMGC_DS12493,BMG_DS041337,Perry Syndrome
+BMGC_DS12494,BMG_DS041338,"PARKINSON DISEASE 1, AUTOSOMAL DOMINANT"
+BMGC_DS12495,BMG_DS041340,Parietal Foramina With Cleidocranial Dysplasia
+BMGC_DS12496,BMG_DS041341,parietal foramina
+BMGC_DS12497,BMG_DS041342,parietal foramina 1
+BMGC_DS12498,BMG_DS041343,parastremmatic dwarfism
+BMGC_DS12499,BMG_DS041344,Paramyotonia Congenita Without Cold Paralysis
+BMGC_DS12500,BMG_DS041345,Paragangliomas with Sensorineural Hearing Loss
+BMGC_DS12501,BMG_DS041346,"papillomatosis, florid, of nipple"
+BMGC_DS12502,BMG_DS041347,panic disorder 1
+BMGC_DS12503,BMG_DS041353,Nasopalpebral lipoma coloboma syndrome
+BMGC_DS12504,BMG_DS041354,"palmaris longus muscle, absence of"
+BMGC_DS12505,BMG_DS041355,"NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE"
+BMGC_DS12506,BMG_DS041356,"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"
+BMGC_DS12507,BMG_DS041357,PHOTOPAROXYSMAL RESPONSE 1
+BMGC_DS12508,BMG_DS041358,"Thanatophoric Dysplasia, Type I"
+BMGC_DS12509,BMG_DS041359,"GRISCELLI SYNDROME, TYPE 2"
+BMGC_DS12510,BMG_DS041360,DYSTONIA 12
+BMGC_DS12511,BMG_DS041361,Paroxysmal kinesigenic choreoathetosis
+BMGC_DS12512,BMG_DS041362,"leukemia, chronic lymphocytic, susceptibility to, 2"
+BMGC_DS12513,BMG_DS041363,"EAR, PATELLA, SHORT STATURE SYNDROME"
+BMGC_DS12514,BMG_DS041364,"multiple sclerosis, susceptibility to"
+BMGC_DS12515,BMG_DS041365,Shone complex
+BMGC_DS12516,BMG_DS041368,Periventricular Nodular Heterotopia
+BMGC_DS12517,BMG_DS041371,diabetic encephalopathy
+BMGC_DS12518,BMG_DS041374,penoscrotal transposition
+BMGC_DS12519,BMG_DS041375,Irritable bowel syndrome characterized by constipation
+BMGC_DS12520,BMG_DS041378,"Weill-Marchesani Syndrome, Autosomal Recessive"
+BMGC_DS12521,BMG_DS041379,"Weill-Marchesani Syndrome, Autosomal Dominant"
+BMGC_DS12522,BMG_DS041380,inherited susceptibility to asthma
+BMGC_DS12523,BMG_DS041381,Paroxysmal nonkinesigenic dyskinesia
+BMGC_DS12524,BMG_DS041382,"hypothyroidism, congenital, nongoitrous, 2"
+BMGC_DS12525,BMG_DS041383,Ehlers-Danlos syndrome spondylodysplastic type 2
+BMGC_DS12526,BMG_DS041384,Limb-girdle muscular dystrophy type 2A
+BMGC_DS12527,BMG_DS041385,"CEROID LIPOFUSCINOSIS, NEURONAL, 2"
+BMGC_DS12528,BMG_DS041387,Copper-Overload Cirrhosis
+BMGC_DS12529,BMG_DS041392,"asthma, aspirin-induced, susceptibility to"
+BMGC_DS12530,BMG_DS041393,Ataxia-Telangiectasia Variant
+BMGC_DS12531,BMG_DS041395,"restless legs syndrome, susceptibility to, 1"
+BMGC_DS12532,BMG_DS041396,"arteries, anomalies of"
+BMGC_DS12533,BMG_DS041397,"EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS"
+BMGC_DS12534,BMG_DS041398,"NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2"
+BMGC_DS12535,BMG_DS041399,calcaneonavicular coalition
+BMGC_DS12536,BMG_DS041400,Dysgnathia complex
+BMGC_DS12537,BMG_DS041401,"TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL"
+BMGC_DS12538,BMG_DS041402,frontonasal dysplasia
+BMGC_DS12539,BMG_DS041404,Hereditary bundle branch system defect
+BMGC_DS12540,BMG_DS041405,acute myeloblastic leukemia with maturation
+BMGC_DS12541,BMG_DS041408,Hypertyrosinemia
+BMGC_DS12542,BMG_DS041414,Inappropriate sinus tachycardia
+BMGC_DS12543,BMG_DS041421,uterine corpus cancer
+BMGC_DS12544,BMG_DS041431,Human Herpesvirus 6 encephalitis
+BMGC_DS12545,BMG_DS041434,Glucocorticoid deficiency
+BMGC_DS12546,BMG_DS041445,T-cell large granular lymphocyte leukemia
+BMGC_DS12547,BMG_DS041446,Malformations of Cortical Development
+BMGC_DS12548,BMG_DS041447,Classical Lissencephalies and Subcortical Band Heterotopias
+BMGC_DS12549,BMG_DS041449,Trichothiodystrophy Syndromes
+BMGC_DS12550,BMG_DS041451,Paris-Trousseau Thrombocytopenia
+BMGC_DS12551,BMG_DS041452,Wolf-Hirschhorn Syndrome
+BMGC_DS12552,BMG_DS041453,Alagille Syndrome 1
+BMGC_DS12553,BMG_DS041454,microlissencephaly
+BMGC_DS12554,BMG_DS041456,"Hematoma, Basal Ganglia"
+BMGC_DS12555,BMG_DS041459,Pulmonary Stenosis
+BMGC_DS12556,BMG_DS041460,Familial Thrombotic Thrombocytopenic Purpura
+BMGC_DS12557,BMG_DS041461,Coronary Artery Disease
+BMGC_DS12558,BMG_DS041462,"Cerebral Amyloid Angiopathy, Genetic"
+BMGC_DS12559,BMG_DS041464,Cranial Arteritis
+BMGC_DS12560,BMG_DS041465,Temporal Arteritis
+BMGC_DS12561,BMG_DS041469,"Double Outlet Right Ventricle, Subaortic VSD"
+BMGC_DS12562,BMG_DS041473,PTEN Hamartoma Tumor Syndrome
+BMGC_DS12563,BMG_DS041474,Myocardial Failure
+BMGC_DS12564,BMG_DS041478,Dihydropyrimidine Dehydrogenase Deficiency
+BMGC_DS12565,BMG_DS041479,Mevalonic Aciduria
+BMGC_DS12566,BMG_DS041484,Calcium renal calculus
+BMGC_DS12567,BMG_DS041499,Aphthous ulceration of skin and/or mucous membrane (disorder)
+BMGC_DS12568,BMG_DS041545,HER2 positive breast carcinoma
+BMGC_DS12569,BMG_DS041558,Hereditary angioedema with normal C1 esterase inhibitor activity
+BMGC_DS12570,BMG_DS041561,Left ventricular noncompaction
+BMGC_DS12571,BMG_DS041572,Aromatase deficiency
+BMGC_DS12572,BMG_DS041593,Long-chain fatty acid transport deficiency
+BMGC_DS12573,BMG_DS041602,Crohn's disease in remission
+BMGC_DS12574,BMG_DS041621,Right-sided Staphylococcus aureus endocarditis
+BMGC_DS12575,BMG_DS041630,T-cell acute lymphoblastic leukemia
+BMGC_DS12576,BMG_DS041635,"Gaucher Disease, Type 1"
+BMGC_DS12577,BMG_DS041641,Spinocerebellar Ataxia 10
+BMGC_DS12578,BMG_DS041652,"ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS"
+BMGC_DS12579,BMG_DS041653,"Xeroderma Pigmentosum, Type G-Cockayne Syndrome"
+BMGC_DS12580,BMG_DS041654,Respiratory Distress Syndrome In Premature Infants
+BMGC_DS12581,BMG_DS041655,"Surfactant Metabolism Dysfunction, Pulmonary, 1"
+BMGC_DS12582,BMG_DS041656,"Osteopetrosis, Autosomal Recessive 5"
+BMGC_DS12583,BMG_DS041657,"Microphthalmia With Hyperopia, Retinal Degeneration, Macrophakia, And Dental Anomalies"
+BMGC_DS12584,BMG_DS041658,"leprosy, susceptibility to, 3"
+BMGC_DS12585,BMG_DS041659,hyper IgE recurrent infection syndrome 1
+BMGC_DS12586,BMG_DS041661,Glycogen Storage Disease IIIA
+BMGC_DS12587,BMG_DS041662,Glycogen Storage Disease IIIB
+BMGC_DS12588,BMG_DS041663,Glycogen Storage Disease IIIC
+BMGC_DS12589,BMG_DS041666,"Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement"
+BMGC_DS12590,BMG_DS041668,"MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES"
+BMGC_DS12591,BMG_DS041669,"Plasminogen Deficiency, Type I"
+BMGC_DS12592,BMG_DS041672,"Microphthalmia, Isolated, with Coloboma 5"
+BMGC_DS12593,BMG_DS041673,"Primary Lateral Sclerosis, Adult, 1"
+BMGC_DS12594,BMG_DS041674,"Febrile Convulsions, Familial, 9"
+BMGC_DS12595,BMG_DS041675,"Epilepsy, Familial Temporal Lobe, 4"
+BMGC_DS12596,BMG_DS041676,"Epilepsy, Familial Mesial Temporal Lobe"
+BMGC_DS12597,BMG_DS041677,"Preauricular Tag, Isolated, Autosomal Dominant, 1"
+BMGC_DS12598,BMG_DS041678,"autism, susceptibility to, 1"
+BMGC_DS12599,BMG_DS041679,congenital anomaly of kidney and urinary tract
+BMGC_DS12600,BMG_DS041680,"CARDIOMYOPATHY, DILATED, 1X"
+BMGC_DS12601,BMG_DS041681,Lissencephaly 3
+BMGC_DS12602,BMG_DS041684,"Cataract, Autosomal Dominant, Multiple Types 1"
+BMGC_DS12603,BMG_DS041685,"Renal Tubular Acidosis, Distal, With Hemolytic Anemia"
+BMGC_DS12604,BMG_DS041686,"Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology"
+BMGC_DS12605,BMG_DS041687,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2M"
+BMGC_DS12606,BMG_DS041688,OTOSCLEROSIS 7
+BMGC_DS12607,BMG_DS041689,OTOSCLEROSIS 4
+BMGC_DS12608,BMG_DS041690,"MECKEL SYNDROME, TYPE 5"
+BMGC_DS12609,BMG_DS041691,JOUBERT SYNDROME 7
+BMGC_DS12610,BMG_DS041692,"Glycogen Storage Disease 0, Muscle"
+BMGC_DS12611,BMG_DS041693,"Renal Tubular Acidosis, Distal, With Nephrocalcinosis, Short Stature, Mental Retardation, And Distinctive Facies"
+BMGC_DS12612,BMG_DS041694,LEOPARD SYNDROME 2
+BMGC_DS12613,BMG_DS041695,Noonan Syndrome 5
+BMGC_DS12614,BMG_DS041696,Premature Ovarian Failure 5
+BMGC_DS12615,BMG_DS041697,"Cataract, Congenital Nuclear, Autosomal Recessive 3"
+BMGC_DS12616,BMG_DS041698,familial cavitary optic disk anomaly
+BMGC_DS12617,BMG_DS041700,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 12"
+BMGC_DS12618,BMG_DS041701,Pontocerebellar Hypoplasia Type 6
+BMGC_DS12619,BMG_DS041702,Tyrosine Kinase 2 Deficiency
+BMGC_DS12620,BMG_DS041704,NEPHRONOPHTHISIS 7
+BMGC_DS12621,BMG_DS041705,"Osteopetrosis, Autosomal Recessive 6"
+BMGC_DS12622,BMG_DS041706,"Atrial Fibrillation, Familial, 5"
+BMGC_DS12623,BMG_DS041707,"Osteopetrosis, Autosomal Recessive 4"
+BMGC_DS12624,BMG_DS041710,GALLBLADDER DISEASE 4
+BMGC_DS12625,BMG_DS041711,"PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED"
+BMGC_DS12626,BMG_DS041712,"Pulmonary Hypertension, Primary, Fenfluramine-Associated"
+BMGC_DS12627,BMG_DS041714,Trifunctional Protein Deficiency With Myopathy And Neuropathy
+BMGC_DS12628,BMG_DS041718,"intellectual disability, autosomal dominant 1"
+BMGC_DS12629,BMG_DS041721,"DEAFNESS, AUTOSOMAL RECESSIVE 63"
+BMGC_DS12630,BMG_DS041722,Neurofibromatosis type 1-like syndrome
+BMGC_DS12631,BMG_DS041724,"Cardiomyopathy, Dilated, 1w"
+BMGC_DS12632,BMG_DS041726,"Cataract, Cortical, Juvenile-Onset"
+BMGC_DS12633,BMG_DS041727,"Ataxia, Spastic, 3, Autosomal Recessive"
+BMGC_DS12634,BMG_DS041730,"Macular Degeneration, Age-Related, 9"
+BMGC_DS12635,BMG_DS041731,Brachydactyly type B2
+BMGC_DS12636,BMG_DS041732,MUNGAN SYNDROME
+BMGC_DS12637,BMG_DS041733,lethal congenital contracture syndrome 3
+BMGC_DS12638,BMG_DS041734,"MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 4"
+BMGC_DS12639,BMG_DS041735,Atrial Septal Defect 4
+BMGC_DS12640,BMG_DS041736,"autism, susceptibility to, 8"
+BMGC_DS12641,BMG_DS041737,"Persistent Hyperplastic Primary Vitreous, Autosomal Recessive"
+BMGC_DS12642,BMG_DS041739,"Muscular Dystrophy, Limb-Girdle, Type 2L"
+BMGC_DS12643,BMG_DS041740,"Ataxia, Spastic, 2, Autosomal Recessive"
+BMGC_DS12644,BMG_DS041741,"Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation"
+BMGC_DS12645,BMG_DS041742,"Dystonia, Focal, Task-Specific"
+BMGC_DS12646,BMG_DS041743,Isobutyryl-CoA dehydrogenase deficiency
+BMGC_DS12647,BMG_DS041744,"febrile seizures, familial, 8"
+BMGC_DS12648,BMG_DS041745,"Glaucoma 1, Open Angle, H"
+BMGC_DS12649,BMG_DS041749,"intellectual disability, FRA12A type"
+BMGC_DS12650,BMG_DS041752,Asphyxiating Thoracic Dystrophy 2
+BMGC_DS12651,BMG_DS041753,"SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE"
+BMGC_DS12652,BMG_DS041755,"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J"
+BMGC_DS12653,BMG_DS041757,"restless legs syndrome, susceptibility to, 6"
+BMGC_DS12654,BMG_DS041758,"Congenital Disorder Of Glycosylation, Type IIH"
+BMGC_DS12655,BMG_DS041759,"Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility"
+BMGC_DS12656,BMG_DS041760,"malaria, susceptibility to"
+BMGC_DS12657,BMG_DS041763,"Bpes, Type I, Autosomal Recessive"
+BMGC_DS12658,BMG_DS041764,spastic ataxia 1
+BMGC_DS12659,BMG_DS041765,AROMATASE EXCESS SYNDROME
+BMGC_DS12660,BMG_DS041768,"CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED"
+BMGC_DS12661,BMG_DS041769,"Angioma serpiginosum, autosomal dominant"
+BMGC_DS12662,BMG_DS041774,Paroxysmal Nonkinesigenic Dyskinesia 2
+BMGC_DS12663,BMG_DS041776,"MECKEL SYNDROME, TYPE 4"
+BMGC_DS12664,BMG_DS041778,Retinitis Pigmentosa 37
+BMGC_DS12665,BMG_DS041779,"Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of"
+BMGC_DS12666,BMG_DS041781,"intellectual disability, autosomal recessive 4"
+BMGC_DS12667,BMG_DS041782,Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation
+BMGC_DS12668,BMG_DS041783,"Deafness, Sensorineural, And Male Infertility"
+BMGC_DS12669,BMG_DS041785,"intellectual disability, autosomal recessive 11"
+BMGC_DS12670,BMG_DS041786,"intellectual disability, autosomal recessive 10"
+BMGC_DS12671,BMG_DS041787,"intellectual disability, autosomal recessive 9"
+BMGC_DS12672,BMG_DS041788,"intellectual disability, autosomal recessive 7"
+BMGC_DS12673,BMG_DS041789,"intellectual disability, autosomal recessive 6"
+BMGC_DS12674,BMG_DS041790,"intellectual disability, autosomal recessive 5"
+BMGC_DS12675,BMG_DS041791,"intellectual disability, autosomal recessive 12"
+BMGC_DS12676,BMG_DS041792,"Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy"
+BMGC_DS12677,BMG_DS041793,Inflammatory Bowel Disease 10
+BMGC_DS12678,BMG_DS041795,"Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4"
+BMGC_DS12679,BMG_DS041796,"asthma-related traits, susceptibility to, 5"
+BMGC_DS12680,BMG_DS041798,"Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen"
+BMGC_DS12681,BMG_DS041799,"Microphthalmia, Isolated 3"
+BMGC_DS12682,BMG_DS041800,Episodic Kinesigenic Dyskinesia 2
+BMGC_DS12683,BMG_DS041801,"DEAFNESS, AUTOSOMAL RECESSIVE, 24"
+BMGC_DS12684,BMG_DS041802,"autism, susceptibility to, 10"
+BMGC_DS12685,BMG_DS041803,"autism, susceptibility to, 9"
+BMGC_DS12686,BMG_DS041806,"prostate cancer, hereditary, 9"
+BMGC_DS12687,BMG_DS041807,Phosphoserine Aminotransferase Deficiency
+BMGC_DS12688,BMG_DS041808,"leprosy, susceptibility to, 4"
+BMGC_DS12689,BMG_DS041809,"Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress"
+BMGC_DS12690,BMG_DS041810,Choreoathetosis And Congenital Hypothyroidism
+BMGC_DS12691,BMG_DS041811,"Tooth Agenesis, Selective, 3"
+BMGC_DS12692,BMG_DS041812,"Progressive Familial Heart Block, Type Ib"
+BMGC_DS12693,BMG_DS041813,"Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation"
+BMGC_DS12694,BMG_DS041815,"Congenital Disorder Of Glycosylation, Type IIF"
+BMGC_DS12695,BMG_DS041816,"Cataract, Posterior Polar, 4, With Microphthalmia And Neurodevelopmental Abnormalities"
+BMGC_DS12696,BMG_DS041817,XFE Progeroid Syndrome
+BMGC_DS12697,BMG_DS041818,PITT-HOPKINS SYNDROME
+BMGC_DS12698,BMG_DS041820,"Coronary Artery Disease, Autosomal Dominant 2"
+BMGC_DS12699,BMG_DS041821,"coronary heart disease, susceptibility to, 7"
+BMGC_DS12700,BMG_DS041822,"systemic lupus erythematosus, susceptibility to, 9"
+BMGC_DS12701,BMG_DS041823,"Surfactant Metabolism Dysfunction, Pulmonary, 3"
+BMGC_DS12702,BMG_DS041824,"Osteogenesis imperfecta, type VIII"
+BMGC_DS12703,BMG_DS041826,"Surfactant Metabolism Dysfunction, Pulmonary, 2"
+BMGC_DS12704,BMG_DS041827,"PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED"
+BMGC_DS12705,BMG_DS041831,Branchiootorenal Syndrome 2
+BMGC_DS12706,BMG_DS041832,Vesicoureteral Reflux 2
+BMGC_DS12707,BMG_DS041834,"CILIARY DYSKINESIA, PRIMARY, 6"
+BMGC_DS12708,BMG_DS041837,multiple endocrine neoplasia type 4
+BMGC_DS12709,BMG_DS041838,"Hirschsprung disease, susceptibility to, 5"
+BMGC_DS12710,BMG_DS041839,"Tooth Agenesis, Selective, X-Linked, 1"
+BMGC_DS12711,BMG_DS041842,"Fabry Disease, Cardiac Variant"
+BMGC_DS12712,BMG_DS041843,"Mental Retardation, X-Linked, Syndromic 14"
+BMGC_DS12713,BMG_DS041844,Phosphoribosylpyrophosphate Synthetase Superactivity
+BMGC_DS12714,BMG_DS041845,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93"
+BMGC_DS12715,BMG_DS041846,Phosphoglycerate Kinase 1 Deficiency
+BMGC_DS12716,BMG_DS041847,"Atypical Mycobacteriosis, Familial, X-Linked 2"
+BMGC_DS12717,BMG_DS041848,IMMUNODEFICIENCY 33
+BMGC_DS12718,BMG_DS041859,Potassium depletion
+BMGC_DS12719,BMG_DS041954,Chlamydia trachomatis infection of genital structure
+BMGC_DS12720,BMG_DS041958,Left ventricular cardiac dysfunction
+BMGC_DS12721,BMG_DS041996,Osteomyelitis caused by Staphylococcus aureus
+BMGC_DS12722,BMG_DS042014,Citrin deficiency
+BMGC_DS12723,BMG_DS042157,Oesophageal reflux (& [without mention of oesophagitis])
+BMGC_DS12724,BMG_DS042159,Vascular insufficiency of intestine
+BMGC_DS12725,BMG_DS042256,glycogen-rich clear cell breast carcinoma
+BMGC_DS12726,BMG_DS042282,ovarian squamous cell carcinoma
+BMGC_DS12727,BMG_DS042286,"Stickler syndrome, type 1"
+BMGC_DS12728,BMG_DS042308,Group B Streptococcal Infection
+BMGC_DS12729,BMG_DS042349,diffuse large B-cell lymphoma of the central nervous system
+BMGC_DS12730,BMG_DS042351,X-linked cerebral adrenoleukodystrophy
+BMGC_DS12731,BMG_DS042352,Haemophilus influenzae Type b Infection
+BMGC_DS12732,BMG_DS042357,pancreatic vasoactive intestinal peptide producing tumor
+BMGC_DS12733,BMG_DS042390,Mixed hyperlipidemia (disorder)
+BMGC_DS12734,BMG_DS042400,indolent plasma cell myeloma
+BMGC_DS12735,BMG_DS042403,pectus excavatum
+BMGC_DS12736,BMG_DS042428,testicular non-seminomatous germ cell tumor
+BMGC_DS12737,BMG_DS042432,congenital fibrinogen deficiency
+BMGC_DS12738,BMG_DS042433,Hypercortisolism due to macronodular adrenal hyperplasia
+BMGC_DS12739,BMG_DS042442,Acute pyelonephritis caused by bacterium
+BMGC_DS12740,BMG_DS042454,Pneumonia caused by Acinetobacter
+BMGC_DS12741,BMG_DS042466,pancreatic mucinous cystadenocarcinoma
+BMGC_DS12742,BMG_DS042469,extrahepatic bile duct rhabdomyosarcoma
+BMGC_DS12743,BMG_DS042584,"Postoperative Pain, Chronic"
+BMGC_DS12744,BMG_DS042590,Influenza due to Influenza A virus subtype H1N1
+BMGC_DS12745,BMG_DS042724,tic disorder
+BMGC_DS12746,BMG_DS042802,extrahepatic bile duct sarcoma
+BMGC_DS12747,BMG_DS042808,ovarian small cell carcinoma
+BMGC_DS12748,BMG_DS042926,"Brucellosis, Pulmonary"
+BMGC_DS12749,BMG_DS042978,hepatocellular carcinoma
+BMGC_DS12750,BMG_DS042988,"DEAFNESS, AUTOSOMAL RECESSIVE 74"
+BMGC_DS12751,BMG_DS042994,Infection of bone
+BMGC_DS12752,BMG_DS043002,Phantosmia
+BMGC_DS12753,BMG_DS043004,oromandibular dystonia
+BMGC_DS12754,BMG_DS043005,Cardio-Renal Syndrome
+BMGC_DS12755,BMG_DS043008,Besnier's prurigo
+BMGC_DS12756,BMG_DS043031,Trichilemmal cyst
+BMGC_DS12757,BMG_DS043032,bulimia nervosa
+BMGC_DS12758,BMG_DS043035,Chronic idiopathic neutropenia
+BMGC_DS12759,BMG_DS043036,Neonatal Hypotonia
+BMGC_DS12760,BMG_DS043039,familial atypical multiple mole melanoma syndrome
+BMGC_DS12761,BMG_DS043043,Pediatric failure to thrive
+BMGC_DS12762,BMG_DS043094,Cryopyrin-Associated Periodic Syndromes
+BMGC_DS12763,BMG_DS043123,Chronic kidney disease stage 5
+BMGC_DS12764,BMG_DS043131,Fetal Pyelectasis
+BMGC_DS12765,BMG_DS043157,microscopic polyangiitis
+BMGC_DS12766,BMG_DS043159,Short Qt Syndrome
+BMGC_DS12767,BMG_DS043161,Acute Anterior Wall Myocardial Infarction
+BMGC_DS12768,BMG_DS043172,Pneumonia caused by Staphylococcus aureus
+BMGC_DS12769,BMG_DS043203,Tinea barbae
+BMGC_DS12770,BMG_DS043204,Viral Croup
+BMGC_DS12771,BMG_DS043205,Postintubation Croup
+BMGC_DS12772,BMG_DS043206,"Clinically Isolated Syndrome, CNS Demyelinating"
+BMGC_DS12773,BMG_DS043209,Polymorphic Reticulosis
+BMGC_DS12774,BMG_DS043210,Unilateral Nasal Obstruction
+BMGC_DS12775,BMG_DS043211,Bilateral Nasal Obstruction
+BMGC_DS12776,BMG_DS043212,Antley-Bixler Syndrome Phenotype
+BMGC_DS12777,BMG_DS043214,Lumbarsacral Spondylosis
+BMGC_DS12778,BMG_DS043215,"Osteoarthritis, Spine"
+BMGC_DS12779,BMG_DS043218,Chronic Lung Injury
+BMGC_DS12780,BMG_DS043228,Resorption Pulmonary Atelectasis
+BMGC_DS12781,BMG_DS043229,Contraction Pulmonary Atelectasis
+BMGC_DS12782,BMG_DS043230,Postoperative Pulmonary Atelectasis
+BMGC_DS12783,BMG_DS043231,Beryllium Disease
+BMGC_DS12784,BMG_DS043232,Constrictive Bronchiolitis
+BMGC_DS12785,BMG_DS043233,"Bronchiolitis, Exudative"
+BMGC_DS12786,BMG_DS043234,Focal Emphysema
+BMGC_DS12787,BMG_DS043235,Tropical Eosinophilic Pneumonia
+BMGC_DS12788,BMG_DS043236,"Bronchiolitis, Proliferative"
+BMGC_DS12789,BMG_DS043242,Pediatric Obesity
+BMGC_DS12790,BMG_DS043248,Vitamin D-resistant rickets
+BMGC_DS12791,BMG_DS043249,Vitamin D-resistant osteomalacia
+BMGC_DS12792,BMG_DS043251,Benign Rolandic Epilepsy
+BMGC_DS12793,BMG_DS043252,T-cell prolymphocytic leukemia
+BMGC_DS12794,BMG_DS043256,Myopic Astigmatism
+BMGC_DS12795,BMG_DS043257,angiocentric glioma
+BMGC_DS12796,BMG_DS043259,Chronic thromboembolic pulmonary hypertension
+BMGC_DS12797,BMG_DS043270,Systemic sclerosis [scleroderma]
+BMGC_DS12798,BMG_DS043283,Hereditary protein S deficiency
+BMGC_DS12799,BMG_DS043284,"Thrombophilia, hereditary"
+BMGC_DS12800,BMG_DS043296,Congenital hypofibrinogenemia
+BMGC_DS12801,BMG_DS043308,Qualitative platelet disorder
+BMGC_DS12802,BMG_DS043340,Hereditary antithrombin III deficiency
+BMGC_DS12803,BMG_DS043352,Allergic rhinitis (disorder)
+BMGC_DS12804,BMG_DS043353,"Carney Complex, Type 1"
+BMGC_DS12805,BMG_DS043356,Unilateral deafness
+BMGC_DS12806,BMG_DS043358,Folliculitis decalvans
+BMGC_DS12807,BMG_DS043359,trilateral retinoblastoma
+BMGC_DS12808,BMG_DS043360,hereditary renal cell carcinoma
+BMGC_DS12809,BMG_DS043361,"Renal Hypoplasia, Isolated"
+BMGC_DS12810,BMG_DS043362,"Cholestasis, benign recurrent intrahepatic 2"
+BMGC_DS12811,BMG_DS043363,"Epidermolysis Bullosa, Junctional, Localisata Variant"
+BMGC_DS12812,BMG_DS043364,"neuronopathy, distal hereditary motor, type 2B"
+BMGC_DS12813,BMG_DS043367,Antisynthetase syndrome
+BMGC_DS12814,BMG_DS043369,Autoimmune Pancreatitis
+BMGC_DS12815,BMG_DS043373,low phospholipid associated cholelithiasis
+BMGC_DS12816,BMG_DS043377,acute kidney failure
+BMGC_DS12817,BMG_DS043379,"Aortic Aneurysm, Familial Thoracic 6"
+BMGC_DS12818,BMG_DS043380,"Erythrocytosis, Familial, 4"
+BMGC_DS12819,BMG_DS043381,Brugada Syndrome 2
+BMGC_DS12820,BMG_DS043382,"Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps"
+BMGC_DS12821,BMG_DS043383,LIPOPROTEIN GLOMERULOPATHY
+BMGC_DS12822,BMG_DS043384,Familial Cold Autoinflammatory Syndrome 2
+BMGC_DS12823,BMG_DS043386,Brain Tumor-Polyposis Syndrome 2
+BMGC_DS12824,BMG_DS043387,progressive myoclonic epilepsy type 3
+BMGC_DS12825,BMG_DS043388,"KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY"
+BMGC_DS12826,BMG_DS043389,"Mucolipidosis III Alpha Beta, Atypical"
+BMGC_DS12827,BMG_DS043390,Mucolipidosis II Alpha Beta
+BMGC_DS12828,BMG_DS043391,"Hypophosphatasia, Perinatal Lethal"
+BMGC_DS12829,BMG_DS043393,Hypergonadotropic Hypogonadism And Partial Alopecia
+BMGC_DS12830,BMG_DS043394,"Leydig Cell Hypoplasia, Type II"
+BMGC_DS12831,BMG_DS043395,"microvascular complications of diabetes, susceptibility to, 7"
+BMGC_DS12832,BMG_DS043396,"Dystonia, Dopa-Responsive, With Or Without Hyperphenylalaninemia, Autosomal Recessive"
+BMGC_DS12833,BMG_DS043397,Combined Cellular And Humoral Immune Defects With Granulomas
+BMGC_DS12834,BMG_DS043400,"Epidermolysis Bullosa Dystrophica, Autosomal Recessive, Localisata Variant"
+BMGC_DS12835,BMG_DS043401,"Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive"
+BMGC_DS12836,BMG_DS043402,"Hypothyroidism, Congenital, Nongoitrous, 5"
+BMGC_DS12837,BMG_DS043404,Combined Saposin Deficiency
+BMGC_DS12838,BMG_DS043405,Combined Oxidative Phosphorylation Deficiency 5
+BMGC_DS12839,BMG_DS043406,"Hypomagnesemia 4, Renal"
+BMGC_DS12840,BMG_DS043407,Spondyloepiphyseal Dysplasia-Brachydactyly and Distinctive Speech
+BMGC_DS12841,BMG_DS043408,"migraine with or without aura, susceptibility to, 12"
+BMGC_DS12842,BMG_DS043409,"Myopathy, Early-Onset, with Fatal Cardiomyopathy"
+BMGC_DS12843,BMG_DS043411,Dystonia with Cerebellar Atrophy
+BMGC_DS12844,BMG_DS043412,Dibasic Amino Aciduria I
+BMGC_DS12845,BMG_DS043413,"Deafness, Autosomal Recessive 1A"
+BMGC_DS12846,BMG_DS043414,"Deafness, Digenic, Gjb2-Gjb6"
+BMGC_DS12847,BMG_DS043415,"Deafness, Digenic, Gjb2-Gjb3"
+BMGC_DS12848,BMG_DS043417,Ciliary Dyskinesia With Transposition Of Ciliary Microtubules
+BMGC_DS12849,BMG_DS043418,BARDET-BIEDL SYNDROME 13
+BMGC_DS12850,BMG_DS043419,Bardet-Biedl Syndrome 14
+BMGC_DS12851,BMG_DS043420,renal-hepatic-pancreatic dysplasia
+BMGC_DS12852,BMG_DS043421,Renal hepatic pancreatic dysplasia Dandy Walker cyst
+BMGC_DS12853,BMG_DS043422,"Anemia, Hypochromic Microcytic, With Iron Overload"
+BMGC_DS12854,BMG_DS043423,"Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive"
+BMGC_DS12855,BMG_DS043424,"Amelogenesis Imperfecta, Hypomaturation Type, Iia1"
+BMGC_DS12856,BMG_DS043425,"Amelogenesis Imperfecta, Type Ic"
+BMGC_DS12857,BMG_DS043426,foveal hypoplasia
+BMGC_DS12858,BMG_DS043427,"Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma"
+BMGC_DS12859,BMG_DS043428,R BINDER DEFICIENCY WITH LACTOFERRIN DEFICIENCY
+BMGC_DS12860,BMG_DS043432,Inflammatory Bowel Disease 11
+BMGC_DS12861,BMG_DS043435,severe achondroplasia-developmental delay-acanthosis nigricans syndrome
+BMGC_DS12862,BMG_DS043436,"Spherocytosis, Type 1"
+BMGC_DS12863,BMG_DS043437,"SPHEROCYTOSIS, HEREDITARY, 2"
+BMGC_DS12864,BMG_DS043439,"Neuromuscular Disease, Congenital, With Uniform Type 1 Fiber"
+BMGC_DS12865,BMG_DS043440,"Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant"
+BMGC_DS12866,BMG_DS043444,"Seizures, intractable"
+BMGC_DS12867,BMG_DS043447,Palmoplantar Hyperkeratosis And True Hermaphroditism
+BMGC_DS12868,BMG_DS043448,"Aortic aneurysm, familial thoracic 3"
+BMGC_DS12869,BMG_DS043451,"microvascular complications of diabetes, susceptibility to, 5"
+BMGC_DS12870,BMG_DS043453,"Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant"
+BMGC_DS12871,BMG_DS043454,"Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy"
+BMGC_DS12872,BMG_DS043456,RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER
+BMGC_DS12873,BMG_DS043457,Myokymia 1
+BMGC_DS12874,BMG_DS043458,Faciocardiomelic Syndrome
+BMGC_DS12875,BMG_DS043459,"alcohol sensitivity, acute"
+BMGC_DS12876,BMG_DS043460,Chromosome 10q26 Deletion Syndrome
+BMGC_DS12877,BMG_DS043461,Chromosome 3q29 Deletion Syndrome
+BMGC_DS12878,BMG_DS043462,"Dandy-Walker Malformation With Occipital Cephalocele, Autosomal Dominant"
+BMGC_DS12879,BMG_DS043463,Mullerian Aplasia and Hyperandrogenism
+BMGC_DS12880,BMG_DS043465,Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus
+BMGC_DS12881,BMG_DS043468,"microvascular complications of diabetes, susceptibility to, 4"
+BMGC_DS12882,BMG_DS043469,"microvascular complications of diabetes, susceptibility to, 6"
+BMGC_DS12883,BMG_DS043470,"Hypospadias 3, Autosomal"
+BMGC_DS12884,BMG_DS043471,Arginine:Glycine Amidinotransferase Deficiency
+BMGC_DS12885,BMG_DS043472,Myopia 15
+BMGC_DS12886,BMG_DS043474,"Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis"
+BMGC_DS12887,BMG_DS043475,Kahrizi Syndrome
+BMGC_DS12888,BMG_DS043476,LEBER CONGENITAL AMAUROSIS 13
+BMGC_DS12889,BMG_DS043477,"Microcephaly, Primary Autosomal Recessive, 7"
+BMGC_DS12890,BMG_DS043479,"Polymicrogyria, Bilateral Occipital"
+BMGC_DS12891,BMG_DS043480,"Spherocytosis, Type 5"
+BMGC_DS12892,BMG_DS043481,"Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract"
+BMGC_DS12893,BMG_DS043482,Cone-Rod Dystrophy 12
+BMGC_DS12894,BMG_DS043483,"Episodic Ataxia, Type 6"
+BMGC_DS12895,BMG_DS043484,"Spherocytosis, Type 4"
+BMGC_DS12896,BMG_DS043485,Endocrine-Cerebroosteodysplasia
+BMGC_DS12897,BMG_DS043486,"CILIARY DYSKINESIA, PRIMARY, 12"
+BMGC_DS12898,BMG_DS043487,"CILIARY DYSKINESIA, PRIMARY, 11"
+BMGC_DS12899,BMG_DS043488,"Deafness, Autosomal Recessive 1b"
+BMGC_DS12900,BMG_DS043489,"Deafness, Autosomal Dominant 2B"
+BMGC_DS12901,BMG_DS043490,"Deafness, Autosomal Dominant 3B"
+BMGC_DS12902,BMG_DS043491,"Deafness, Autosomal Dominant 59"
+BMGC_DS12903,BMG_DS043492,Inflammatory Bowel Disease 26
+BMGC_DS12904,BMG_DS043496,Duplication 15q11-q13 Syndrome
+BMGC_DS12905,BMG_DS043497,Chromosome 22q11.2 Microduplication Syndrome
+BMGC_DS12906,BMG_DS043498,Capillary Malformation Without Arteriovenous Malformation
+BMGC_DS12907,BMG_DS043499,plasma fibronectin deficiency
+BMGC_DS12908,BMG_DS043500,Desmoid Tumor Caused By Somatic Mutation
+BMGC_DS12909,BMG_DS043502,"Adenylate Kinase Deficiency, Hemolytic Anemia Due To"
+BMGC_DS12910,BMG_DS043504,Chromosome 15q26-Qter Deletion Syndrome
+BMGC_DS12911,BMG_DS043505,"microvascular complications of diabetes, susceptibility to, 3"
+BMGC_DS12912,BMG_DS043506,"microvascular complications of diabetes, susceptibility to, 2"
+BMGC_DS12913,BMG_DS043508,"intellectual disability, autosomal dominant 5"
+BMGC_DS12914,BMG_DS043511,"multiple sclerosis, susceptibility to, 3"
+BMGC_DS12915,BMG_DS043515,"colorectal cancer, susceptibility to, 10"
+BMGC_DS12916,BMG_DS043520,Chromosome 6pter-P24 Deletion Syndrome
+BMGC_DS12917,BMG_DS043521,"intellectual disability, autosomal dominant 4"
+BMGC_DS12918,BMG_DS043522,"intellectual disability, autosomal dominant 3"
+BMGC_DS12919,BMG_DS043523,AMYOTROPHIC LATERAL SCLEROSIS 11
+BMGC_DS12920,BMG_DS043524,Split-Hand-Foot Malformation With Long Bone Deficiency 3
+BMGC_DS12921,BMG_DS043525,Retinitis Pigmentosa 46
+BMGC_DS12922,BMG_DS043527,"INFLAMMATORY BOWEL DISEASE 25, AUTOSOMAL RECESSIVE"
+BMGC_DS12923,BMG_DS043528,Inflammatory Bowel Disease 24
+BMGC_DS12924,BMG_DS043529,Diamond-Blackfan Anemia 8
+BMGC_DS12925,BMG_DS043530,Diamond-Blackfan Anemia 7
+BMGC_DS12926,BMG_DS043534,Adiponectin Deficiency
+BMGC_DS12927,BMG_DS043535,Hypoadiponectinemia
+BMGC_DS12928,BMG_DS043536,"breast-ovarian cancer, familial, susceptibility to, 2"
+BMGC_DS12929,BMG_DS043539,"focal segmental glomerulosclerosis 4, susceptibility to"
+BMGC_DS12930,BMG_DS043540,"Myopathy, Congenital, Compton-North"
+BMGC_DS12931,BMG_DS043541,"Spastic Paraplegia 42, Autosomal Dominant"
+BMGC_DS12932,BMG_DS043542,"lumbar disk degeneration, susceptibility to"
+BMGC_DS12933,BMG_DS043543,"Retinitis Pigmentosa 7, Digenic"
+BMGC_DS12934,BMG_DS043545,familial acute necrotizing encephalopathy
+BMGC_DS12935,BMG_DS043547,osteoarthritis susceptibility 3
+BMGC_DS12936,BMG_DS043549,"Niemann-Pick Disease, Intermediate, Protracted Neurovisceral"
+BMGC_DS12937,BMG_DS043552,Dyschromatosis Universalis Hereditaria 1
+BMGC_DS12938,BMG_DS043553,"Deafness, Congenital, and Onychodystrophy, Autosomal Dominant"
+BMGC_DS12939,BMG_DS043554,"Craniodiaphyseal Dysplasia, Autosomal Dominant"
+BMGC_DS12940,BMG_DS043555,"Deafness, Autosomal Dominant 3A"
+BMGC_DS12941,BMG_DS043556,"EPIPHYSEAL DYSPLASIA, MULTIPLE, 6"
+BMGC_DS12942,BMG_DS043558,Holoprosencephaly 10
+BMGC_DS12943,BMG_DS043559,"Amelogenesis Imperfecta, Hypomaturation Type, Iia2"
+BMGC_DS12944,BMG_DS043560,Diamond-Blackfan Anemia 5
+BMGC_DS12945,BMG_DS043561,Diamond-Blackfan Anemia 4
+BMGC_DS12946,BMG_DS043562,"Lipodystrophy, Congenital Generalized, Type 3"
+BMGC_DS12947,BMG_DS043563,"Pyloric Stenosis, Infantile Hypertrophic, 5"
+BMGC_DS12948,BMG_DS043564,"Diabetes Mellitus, Insulin-Dependent, 22"
+BMGC_DS12949,BMG_DS043566,"Diabetes Mellitus, Insulin-Dependent, 20"
+BMGC_DS12950,BMG_DS043567,"CILIARY DYSKINESIA, PRIMARY, 10"
+BMGC_DS12951,BMG_DS043568,Specific Language Impairment 4
+BMGC_DS12952,BMG_DS043569,Chromosome 2p16.1-P15 Deletion Syndrome
+BMGC_DS12953,BMG_DS043570,Chromosome 1q21.1 Duplication Syndrome
+BMGC_DS12954,BMG_DS043571,chromosome 1q21.1 deletion syndrome
+BMGC_DS12955,BMG_DS043572,"Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome"
+BMGC_DS12956,BMG_DS043573,"schizophrenia, susceptibility to"
+BMGC_DS12957,BMG_DS043576,"Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant"
+BMGC_DS12958,BMG_DS043579,Diamond-Blackfan Anemia 1
+BMGC_DS12959,BMG_DS043581,familial isolated pituitary adenoma
+BMGC_DS12960,BMG_DS043584,"Skeletal Defects, Genital Hypoplasia, And Mental Retardation"
+BMGC_DS12961,BMG_DS043585,Complement Component 6 Deficiency
+BMGC_DS12962,BMG_DS043588,"CILIARY DYSKINESIA, PRIMARY, 9"
+BMGC_DS12963,BMG_DS043589,"Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism"
+BMGC_DS12964,BMG_DS043590,"Leukodystrophy, Hypomyelinating, 6"
+BMGC_DS12965,BMG_DS043591,Prickle1-Related Progressive Myoclonus Epilepsy with Ataxia
+BMGC_DS12966,BMG_DS043592,"Cardiomyopathy, Familial Restrictive, 3"
+BMGC_DS12967,BMG_DS043595,"Dystonia 17, Torsion, Autosomal Recessive"
+BMGC_DS12968,BMG_DS043596,"Bone Fragility with Contractures, Arterial Rupture, and Deafness"
+BMGC_DS12969,BMG_DS043597,Pontocerebellar Hypoplasia Type 2C
+BMGC_DS12970,BMG_DS043598,Pontocerebellar Hypoplasia Type 2B
+BMGC_DS12971,BMG_DS043600,"sarcoidosis, susceptibility to, 2"
+BMGC_DS12972,BMG_DS043601,Inflammatory Bowel Disease 23
+BMGC_DS12973,BMG_DS043602,Inflammatory Bowel Disease 22
+BMGC_DS12974,BMG_DS043604,Cowden-Like Syndrome
+BMGC_DS12975,BMG_DS043605,Inflammatory Bowel Disease 21
+BMGC_DS12976,BMG_DS043606,"Porokeratosis, Disseminated Superficial Actinic, 4"
+BMGC_DS12977,BMG_DS043607,"Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like"
+BMGC_DS12978,BMG_DS043608,"breast-ovarian cancer, familial, susceptibility to, 1"
+BMGC_DS12979,BMG_DS043610,"Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator"
+BMGC_DS12980,BMG_DS043612,Jervell And Lange-Nielsen Syndrome 2
+BMGC_DS12981,BMG_DS043614,Chromosome 1q43-Q44 Deletion Syndrome
+BMGC_DS12982,BMG_DS043615,"Spastic Paraplegia 38, Autosomal Dominant"
+BMGC_DS12983,BMG_DS043616,Chromosome 2q32-Q33 Deletion Syndrome
+BMGC_DS12984,BMG_DS043619,Premature Ovarian Failure 6
+BMGC_DS12985,BMG_DS043620,"THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE"
+BMGC_DS12986,BMG_DS043621,"Osteopetrosis, Autosomal Recessive 7"
+BMGC_DS12987,BMG_DS043622,CD59 Deficiency
+BMGC_DS12988,BMG_DS043624,Birk-Barel Mental Retardation Dysmorphism Syndrome
+BMGC_DS12989,BMG_DS043625,Joubert Syndrome 8
+BMGC_DS12990,BMG_DS043626,"Microtia, Hearing Impairment, And Cleft Palate"
+BMGC_DS12991,BMG_DS043627,FONTAINE PROGEROID SYNDROME
+BMGC_DS12992,BMG_DS043628,Inflammatory Bowel Disease 20
+BMGC_DS12993,BMG_DS043629,"Nephrolithiasis-Osteoporosis, Hypophosphatemic, 2"
+BMGC_DS12994,BMG_DS043630,"Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1"
+BMGC_DS12995,BMG_DS043631,Joubert Syndrome 9
+BMGC_DS12996,BMG_DS043632,"Meckel Syndrome, Type 6"
+BMGC_DS12997,BMG_DS043633,"microvascular complications of diabetes, susceptibility to, 1"
+BMGC_DS12998,BMG_DS043634,"lumbar disk herniation, susceptibility to"
+BMGC_DS12999,BMG_DS043635,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6"
+BMGC_DS13000,BMG_DS043637,Inflammatory Bowel Disease 19
+BMGC_DS13001,BMG_DS043639,"epilepsy, childhood absence, susceptibility to, 5"
+BMGC_DS13002,BMG_DS043641,Inflammatory Bowel Disease 18
+BMGC_DS13003,BMG_DS043642,Inflammatory Bowel Disease 17
+BMGC_DS13004,BMG_DS043643,MYD88 Deficiency
+BMGC_DS13005,BMG_DS043644,Inflammatory Bowel Disease 16
+BMGC_DS13006,BMG_DS043645,Inflammatory Bowel Disease 15
+BMGC_DS13007,BMG_DS043647,"systemic lupus erythematosus, susceptibility to, 11"
+BMGC_DS13008,BMG_DS043648,"systemic lupus erythematosus, susceptibility to, 10"
+BMGC_DS13009,BMG_DS043649,Crouzon syndrome-acanthosis nigricans syndrome
+BMGC_DS13010,BMG_DS043650,Inflammatory Bowel Disease 14
+BMGC_DS13011,BMG_DS043651,Inflammatory Bowel Disease 13
+BMGC_DS13012,BMG_DS043653,Inflammatory Bowel Disease 12
+BMGC_DS13013,BMG_DS043654,"Atrial Fibrillation, Familial, 7"
+BMGC_DS13014,BMG_DS043657,"Leukodystrophy, Hypomyelinating, 4"
+BMGC_DS13015,BMG_DS043658,"Leukodystrophy, hypomyelinating"
+BMGC_DS13016,BMG_DS043662,"colorectal cancer, susceptibility to, 3"
+BMGC_DS13017,BMG_DS043664,maturity-onset diabetes of the young type 9
+BMGC_DS13018,BMG_DS043665,"Lymphedema, Cardiac Septal Defects, And Characteristic Facies"
+BMGC_DS13019,BMG_DS043668,"Atrial Fibrillation, Familial, 6"
+BMGC_DS13020,BMG_DS043669,Coats plus syndrome
+BMGC_DS13021,BMG_DS043670,Diastasis Recti And Weakness Of The Linea Alba
+BMGC_DS13022,BMG_DS043671,Retinitis Pigmentosa 29
+BMGC_DS13023,BMG_DS043672,"Epileptic Encephalopathy, Early Infantile, 4"
+BMGC_DS13024,BMG_DS043675,"Cardiomyopathy, Dilated, 1AA"
+BMGC_DS13025,BMG_DS043676,Epidermolysis Bullosa Simplex With Pyloric Atresia
+BMGC_DS13026,BMG_DS043677,OROFACIAL CLEFT 11
+BMGC_DS13027,BMG_DS043678,"Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant"
+BMGC_DS13028,BMG_DS043679,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12"
+BMGC_DS13029,BMG_DS043680,Oculoauricular Syndrome
+BMGC_DS13030,BMG_DS043681,"autism, susceptibility to, 15"
+BMGC_DS13031,BMG_DS043682,"Trichoepithelioma, Multiple Familial, 2"
+BMGC_DS13032,BMG_DS043683,"Cardiomyopathy, Familial Hypertrophic, 11"
+BMGC_DS13033,BMG_DS043684,"Deafness, Unilateral, With Delayed Endolymphatic Hydrops"
+BMGC_DS13034,BMG_DS043685,Otosclerosis 8
+BMGC_DS13035,BMG_DS043686,Retinitis Pigmentosa 41
+BMGC_DS13036,BMG_DS043687,Hypophosphatemic Rickets And Hyperparathyroidism
+BMGC_DS13037,BMG_DS043688,"Alopecia, Neurologic Defects, and Endocrinopathy Syndrome"
+BMGC_DS13038,BMG_DS043689,"Hypouricemia, Renal, 2"
+BMGC_DS13039,BMG_DS043690,Amyotrophic Lateral Sclerosis 10
+BMGC_DS13040,BMG_DS043691,dystonia 16
+BMGC_DS13041,BMG_DS043693,"Spastic Paraplegia 39, Autosomal Recessive"
+BMGC_DS13042,BMG_DS043694,"Cataract, Juvenile, With Microcornea And Glucosuria"
+BMGC_DS13043,BMG_DS043696,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9"
+BMGC_DS13044,BMG_DS043697,"Congenital Disorder Of Glycosylation, Type In"
+BMGC_DS13045,BMG_DS043698,"celiac disease, susceptibility to, 13"
+BMGC_DS13046,BMG_DS043705,Thrombocytopenia 4
+BMGC_DS13047,BMG_DS043706,Chromosome 15q13.3 Microdeletion Syndrome
+BMGC_DS13048,BMG_DS043707,SCHIZOPHRENIA 14
+BMGC_DS13049,BMG_DS043708,"Deafness, Autosomal Dominant 2A"
+BMGC_DS13050,BMG_DS043709,"Rett Syndrome, Zappella Variant"
+BMGC_DS13051,BMG_DS043711,Hunter-Macdonald Syndrome
+BMGC_DS13052,BMG_DS043712,Stevenson-Carey Syndrome
+BMGC_DS13053,BMG_DS043713,"asthma-related traits, susceptibility to, 7"
+BMGC_DS13054,BMG_DS043717,"Macular Degeneration, Age-Related, 11"
+BMGC_DS13055,BMG_DS043720,Riddle Syndrome
+BMGC_DS13056,BMG_DS043721,"epilepsy, idiopathic generalized, susceptibility to, 6"
+BMGC_DS13057,BMG_DS043722,catecholaminergic polymorphic ventricular tachycardia 2
+BMGC_DS13058,BMG_DS043724,"Camptodactyly Syndrome, Guadalajara, Type III"
+BMGC_DS13059,BMG_DS043725,"prostate cancer, hereditary, 13"
+BMGC_DS13060,BMG_DS043726,"Episodic Ataxia, Type 7"
+BMGC_DS13061,BMG_DS043727,"Surfactant Metabolism Dysfunction, Pulmonary, 4"
+BMGC_DS13062,BMG_DS043728,"Hypospadias 2, X-Linked"
+BMGC_DS13063,BMG_DS043730,"Protoporphyria, Erythropoietic, X-Linked Dominant"
+BMGC_DS13064,BMG_DS043731,"Spastic Paraplegia 34, X-Linked"
+BMGC_DS13065,BMG_DS043732,Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia
+BMGC_DS13066,BMG_DS043733,"Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities"
+BMGC_DS13067,BMG_DS043734,"Myopathy, Reducing Body, X-Linked, Childhood-Onset"
+BMGC_DS13068,BMG_DS043735,"Myopathy, Reducing Body, X-Linked, Early-Onset, Severe"
+BMGC_DS13069,BMG_DS043736,"intellectual disability, X-linked 95"
+BMGC_DS13070,BMG_DS043737,Craniofacioskeletal Syndrome
+BMGC_DS13071,BMG_DS043740,syndromic X-linked intellectual disability Shrimpton type
+BMGC_DS13072,BMG_DS043741,"TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS"
+BMGC_DS13073,BMG_DS043742,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE"
+BMGC_DS13074,BMG_DS043744,"Spinocerebellar Ataxia, X-Linked 5"
+BMGC_DS13075,BMG_DS043745,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, WU TYPE"
+BMGC_DS13076,BMG_DS043746,"Myopathy, X-Linked, With Postural Muscle Atrophy"
+BMGC_DS13077,BMG_DS043747,"SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT"
+BMGC_DS13078,BMG_DS043748,Myofibrillar Myopathy
+BMGC_DS13079,BMG_DS043749,"Hypospadias 1, X-Linked"
+BMGC_DS13080,BMG_DS043750,Periventricular Laminar Heterotopia
+BMGC_DS13081,BMG_DS043753,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE"
+BMGC_DS13082,BMG_DS043754,"Mental Retardation, X-Linked, With Panhypopituitarism"
+BMGC_DS13083,BMG_DS043756,"Hypercarotenemia And Vitamin A Deficiency, Autosomal Recessive"
+BMGC_DS13084,BMG_DS043757,Thrombocytopenia 3
+BMGC_DS13085,BMG_DS043758,Three M Syndrome 1
+BMGC_DS13086,BMG_DS043759,"Spherocytosis, Type 3"
+BMGC_DS13087,BMG_DS043761,"UV-induced skin damage, susceptibility to"
+BMGC_DS13088,BMG_DS043762,"PITUITARY HORMONE DEFICIENCY, COMBINED, 4"
+BMGC_DS13089,BMG_DS043764,"Hyperphenylalaninemia, Non-Pku Mild"
+BMGC_DS13090,BMG_DS043765,CRANIOOSTEOARTHROPATHY
+BMGC_DS13091,BMG_DS043766,Nanophthalmos 3
+BMGC_DS13092,BMG_DS043767,Amyotrophic Lateral Sclerosis 9
+BMGC_DS13093,BMG_DS043770,Lethal Arthrogryposis With Anterior Horn Cell Disease
+BMGC_DS13094,BMG_DS043772,"Ciliary Dyskinesia, Primary, 7"
+BMGC_DS13095,BMG_DS043773,"Cardiomyopathy, Dilated, 2a"
+BMGC_DS13096,BMG_DS043774,"Cardiomyopathy, Dilated, 1z"
+BMGC_DS13097,BMG_DS043775,"Cardiomyopathy, Dilated, 1y"
+BMGC_DS13098,BMG_DS043776,Brugada Syndrome 4
+BMGC_DS13099,BMG_DS043777,Brugada Syndrome 3
+BMGC_DS13100,BMG_DS043778,"prostate cancer, hereditary, 12"
+BMGC_DS13101,BMG_DS043779,"Chromosome 22q11.2 Deletion Syndrome, Distal"
+BMGC_DS13102,BMG_DS043780,Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma
+BMGC_DS13103,BMG_DS043781,Long Qt Syndrome 11
+BMGC_DS13104,BMG_DS043782,Long Qt Syndrome 10
+BMGC_DS13105,BMG_DS043783,Long Qt Syndrome 9
+BMGC_DS13106,BMG_DS043784,Temple-Baraitser Syndrome
+BMGC_DS13107,BMG_DS043785,"Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs"
+BMGC_DS13108,BMG_DS043786,"Tremor, Hereditary Essential, And Idiopathic Normal Pressure Hydrocephalus"
+BMGC_DS13109,BMG_DS043787,Elliptocytosis 1
+BMGC_DS13110,BMG_DS043788,"AXENFELD-RIEGER SYNDROME, TYPE 3"
+BMGC_DS13111,BMG_DS043789,"SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE"
+BMGC_DS13112,BMG_DS043790,"HYPERPIGMENTATION, FAMILIAL PROGRESSIVE, 1"
+BMGC_DS13113,BMG_DS043791,Retinitis Pigmentosa 2
+BMGC_DS13114,BMG_DS043792,"aplastic anemia, susceptibility to"
+BMGC_DS13115,BMG_DS043793,"sarcoidosis, susceptibility to, 1"
+BMGC_DS13116,BMG_DS043794,"46,XY ovotesticular disorder of sex development"
+BMGC_DS13117,BMG_DS043796,nevus flammeus of nape of neck
+BMGC_DS13118,BMG_DS043797,Loeys-Dietz Syndrome
+BMGC_DS13119,BMG_DS043798,B-lymphoblastic leukemia/lymphoma with hyperdiploidy
+BMGC_DS13120,BMG_DS043799,B-lymphoblastic leukemia/lymphoma with hypodiploidy
+BMGC_DS13121,BMG_DS043800,B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality
+BMGC_DS13122,BMG_DS043801,B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)
+BMGC_DS13123,BMG_DS043805,split hand
+BMGC_DS13124,BMG_DS043807,synpolydactyly
+BMGC_DS13125,BMG_DS043811,Waardenburg syndrome type 2
+BMGC_DS13126,BMG_DS043812,"WAARDENBURG SYNDROME, TYPE IIE"
+BMGC_DS13127,BMG_DS043813,"scoliosis, isolated, susceptibility to, 1"
+BMGC_DS13128,BMG_DS043814,"EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE"
+BMGC_DS13129,BMG_DS043815,"nephrolithiasis, uric acid, susceptibility to"
+BMGC_DS13130,BMG_DS043816,major affective disorder 7
+BMGC_DS13131,BMG_DS043819,Omenn Syndrome
+BMGC_DS13132,BMG_DS043842,Influenza caused by Influenza A virus
+BMGC_DS13133,BMG_DS043846,Steatohepatitis
+BMGC_DS13134,BMG_DS043852,osteonecrosis of the jaw
+BMGC_DS13135,BMG_DS043853,Ischemic priapism
+BMGC_DS13136,BMG_DS043888,Combined immunodeficiency disease
+BMGC_DS13137,BMG_DS043890,Epilepsy characterized by intractable complex partial seizures
+BMGC_DS13138,BMG_DS043904,Lateral cystocele
+BMGC_DS13139,BMG_DS043929,Gout attack
+BMGC_DS13140,BMG_DS043934,Arylsulfatase A Deficiency
+BMGC_DS13141,BMG_DS043935,alpha-L-Iduronidase Deficiency
+BMGC_DS13142,BMG_DS043936,7-Dehydrocholesterol Reductase Deficiency
+BMGC_DS13143,BMG_DS043937,myelodysplastic syndrome
+BMGC_DS13144,BMG_DS043938,"Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency"
+BMGC_DS13145,BMG_DS043939,Haim-Monk Syndrome
+BMGC_DS13146,BMG_DS043940,"Polyposis, Adenomatous Intestinal"
+BMGC_DS13147,BMG_DS043941,Familial Intestinal Polyposis
+BMGC_DS13148,BMG_DS043942,"Hyperpotassemia and Hypertension, Familial"
+BMGC_DS13149,BMG_DS043943,Total Hexosaminidase Deficiency
+BMGC_DS13150,BMG_DS043944,Deficiency of Platelet Glycoprotein 1b
+BMGC_DS13151,BMG_DS043945,Androgen Receptor Deficiency
+BMGC_DS13152,BMG_DS043949,Platelet alpha-Granule Deficiency
+BMGC_DS13153,BMG_DS043952,Steroid Sulfatase Deficiency Disease
+BMGC_DS13154,BMG_DS043953,"Drug-Induced Liver Injury, Chronic"
+BMGC_DS13155,BMG_DS043954,Encapsulating Peritoneal Sclerosis
+BMGC_DS13156,BMG_DS043958,Propionic Aciduria
+BMGC_DS13157,BMG_DS043959,"Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant"
+BMGC_DS13158,BMG_DS043960,Hereditary Angioedema Types I and II
+BMGC_DS13159,BMG_DS043961,Hereditary Angioedema Type I
+BMGC_DS13160,BMG_DS043962,Isolated Noncompaction of the Ventricular Myocardium
+BMGC_DS13161,BMG_DS043966,Thrombotic Microangiopathies
+BMGC_DS13162,BMG_DS043972,Alcoholic Steatohepatitis
+BMGC_DS13163,BMG_DS043973,beta-Galactosidase Deficiency
+BMGC_DS13164,BMG_DS043974,Deficiency of Uroporphyrinogen III Synthase
+BMGC_DS13165,BMG_DS043976,Sulfoiduronate Sulfatase Deficiency
+BMGC_DS13166,BMG_DS043977,Placental Steroid Sulfatase Deficiency
+BMGC_DS13167,BMG_DS043978,"ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY"
+BMGC_DS13168,BMG_DS043979,Fibrosis of pleura
+BMGC_DS13169,BMG_DS043996,Auditory neuropathy spectrum disorder
+BMGC_DS13170,BMG_DS044037,Cerebral Small Vessel Diseases
+BMGC_DS13171,BMG_DS044060,Pulmonary Mycobacterium avium complex infection
+BMGC_DS13172,BMG_DS044061,Disorder of lumbar disc
+BMGC_DS13173,BMG_DS044069,Juvenile-Onset Vitelliform Macular Dystrophy
+BMGC_DS13174,BMG_DS044070,"Hyalinosis, Systemic"
+BMGC_DS13175,BMG_DS044071,Spondylometaphyseal dysplasia with dentinogenesis imperfecta
+BMGC_DS13176,BMG_DS044072,spondyloepiphyseal dysplasia congenita
+BMGC_DS13177,BMG_DS044074,Kashin-Beck Disease
+BMGC_DS13178,BMG_DS044075,Fitzsimmons-McLachlan-Gilbert syndrome
+BMGC_DS13179,BMG_DS044076,OROFACIODIGITAL SYNDROME VI
+BMGC_DS13180,BMG_DS044077,2-Hydroxyglutaricaciduria
+BMGC_DS13181,BMG_DS044079,Congenital idiopathic intestinal pseudoobstruction
+BMGC_DS13182,BMG_DS044080,Familial ectopia lentis
+BMGC_DS13183,BMG_DS044081,"Deafness, Autosomal Recessive 77"
+BMGC_DS13184,BMG_DS044083,Cronobacter Infections
+BMGC_DS13185,BMG_DS044086,Sensorineural Deafness With Mild Renal Dysfunction
+BMGC_DS13186,BMG_DS044088,"leishmaniasis, tegumentary, susceptibility to"
+BMGC_DS13187,BMG_DS044089,"CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS"
+BMGC_DS13188,BMG_DS044092,Orofacial Cleft 12
+BMGC_DS13189,BMG_DS044093,"restless legs syndrome, susceptibility to, 7"
+BMGC_DS13190,BMG_DS044094,INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY
+BMGC_DS13191,BMG_DS044096,"spondyloepimetaphyseal dysplasia, PAPSS2 type"
+BMGC_DS13192,BMG_DS044098,Lumbar scoliosis
+BMGC_DS13193,BMG_DS044099,"Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant"
+BMGC_DS13194,BMG_DS044100,Hypotrichosis 5
+BMGC_DS13195,BMG_DS044101,"Leukocyte Adhesion Deficiency, Type III"
+BMGC_DS13196,BMG_DS044102,Brugada Syndrome 5
+BMGC_DS13197,BMG_DS044103,"Cardiac Conduction Defect, Nonspecific"
+BMGC_DS13198,BMG_DS044104,"Spondyloepimetaphyseal Dysplasia, Aggrecan Type"
+BMGC_DS13199,BMG_DS044105,"question mark ears, isolated"
+BMGC_DS13200,BMG_DS044106,Inflammatory Bowel Disease 27
+BMGC_DS13201,BMG_DS044107,Atrial Septal Defect 5
+BMGC_DS13202,BMG_DS044108,"Deafness, Autosomal Recessive 71"
+BMGC_DS13203,BMG_DS044110,Immune dysfunction with T-cell inactivation due to calcium entry defect 2
+BMGC_DS13204,BMG_DS044111,Immune dysfunction with T-cell inactivation due to calcium entry defect 1
+BMGC_DS13205,BMG_DS044112,"Isolated Growth Hormone Deficiency, Type IB"
+BMGC_DS13206,BMG_DS044113,SeSAME syndrome
+BMGC_DS13207,BMG_DS044115,Hypoglossia With Situs Inversus
+BMGC_DS13208,BMG_DS044119,Mitchell-Riley Syndrome
+BMGC_DS13209,BMG_DS044121,"Vitamin D-Dependent Rickets, Type 2B, With Normal Vitamin D Receptor"
+BMGC_DS13210,BMG_DS044123,"FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULAR INVOLVEMENT"
+BMGC_DS13211,BMG_DS044124,"CARDIOMYOPATHY, INFANTILE HYPERTROPHIC"
+BMGC_DS13212,BMG_DS044125,Ovotesticular Disorders of Sex Development
+BMGC_DS13213,BMG_DS044126,"46,Xy Gonadal Dysgenesis, Complete, Sry-Related"
+BMGC_DS13214,BMG_DS044127,"46,Xy True Hermaphroditism, Sry-Related"
+BMGC_DS13215,BMG_DS044128,"Rett Syndrome, Atypical"
+BMGC_DS13216,BMG_DS044129,Otopalatodigital Spectrum Disorder
+BMGC_DS13217,BMG_DS044131,"Glycogen Storage Disease, Type IXA2"
+BMGC_DS13218,BMG_DS044132,Chromosome Xq28 Duplication Syndrome
+BMGC_DS13219,BMG_DS044134,"Thrombophilia, X-Linked, Due To Factor Ix Defect"
+BMGC_DS13220,BMG_DS044135,Joubert Syndrome 10
+BMGC_DS13221,BMG_DS044136,"intellectual disability, X-linked 97"
+BMGC_DS13222,BMG_DS044137,Chromosome Xp11.23-P11.22 Duplication Syndrome
+BMGC_DS13223,BMG_DS044138,"Corneal Dystrophy, Endothelial, X-Linked"
+BMGC_DS13224,BMG_DS044139,"Corneal Dystrophy, Lisch Epithelial"
+BMGC_DS13225,BMG_DS044140,"Emery-Dreifuss Muscular Dystrophy 6, X-Linked"
+BMGC_DS13226,BMG_DS044141,"Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked"
+BMGC_DS13227,BMG_DS044142,"Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness"
+BMGC_DS13228,BMG_DS044143,"Mineralocorticoid Deficiency, Isolated"
+BMGC_DS13229,BMG_DS044144,"46,XX SEX REVERSAL 2"
+BMGC_DS13230,BMG_DS044145,Vater Association With Macrocephaly And Ventriculomegaly
+BMGC_DS13231,BMG_DS044146,"Gm2-Gangliosidosis, Variant B1"
+BMGC_DS13232,BMG_DS044148,"Refsum Disease, Adult, 1"
+BMGC_DS13233,BMG_DS044149,"Refsum Disease, Adult, 2"
+BMGC_DS13234,BMG_DS044150,"Oculodentodigital Dysplasia, Autosomal Recessive"
+BMGC_DS13235,BMG_DS044151,"neuroblastoma, susceptibility to, 1"
+BMGC_DS13236,BMG_DS044152,"MYOPIA 18, AUTOSOMAL RECESSIVE"
+BMGC_DS13237,BMG_DS044154,"Methemoglobinemia, Type I"
+BMGC_DS13238,BMG_DS044155,"Methemoglobinemia, Type Ii"
+BMGC_DS13239,BMG_DS044156,"Nadh-Cytochrome B5 Reductase Deficiency, Type I"
+BMGC_DS13240,BMG_DS044157,"Nadh-Cytochrome B5 Reductase Deficiency, Type Ii"
+BMGC_DS13241,BMG_DS044159,"AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I, WITH REVERSIBLE METAPHYSEAL DYSPLASIA"
+BMGC_DS13242,BMG_DS044160,"hemolytic uremic syndrome, atypical, susceptibility to, 1"
+BMGC_DS13243,BMG_DS044161,Motor axonal neuropathy
+BMGC_DS13244,BMG_DS044163,"MEGALOBLASTIC ANEMIA, FOLATE-RESPONSIVE"
+BMGC_DS13245,BMG_DS044164,Aicardi-Goutieres syndrome 5
+BMGC_DS13246,BMG_DS044165,Split-Hand-Foot Malformation 6
+BMGC_DS13247,BMG_DS044167,"CYSTINOSIS, ATYPICAL NEPHROPATHIC"
+BMGC_DS13248,BMG_DS044168,BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1
+BMGC_DS13249,BMG_DS044169,"Macrothrombocytopenia-Stomatocytosis, Mediterranean"
+BMGC_DS13250,BMG_DS044172,MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)
+BMGC_DS13251,BMG_DS044173,"Mitochondrial Neurogastrointestinal Encephalopathy Syndrome, Rrm2b-Related"
+BMGC_DS13252,BMG_DS044174,Mitochondrial DNA depletion syndrome encephalomyopathic form with methylmalonic aciduria
+BMGC_DS13253,BMG_DS044175,"epilepsy, childhood absence, susceptibility to, 6"
+BMGC_DS13254,BMG_DS044176,Chromosome 3q29 Duplication Syndrome
+BMGC_DS13255,BMG_DS044178,"Spastic Paraplegia 18, Autosomal Recessive"
+BMGC_DS13256,BMG_DS044179,"thyrotoxic periodic paralysis, susceptibility to, 1"
+BMGC_DS13257,BMG_DS044180,Growth Hormone Deficiency With Pituitary Anomalies
+BMGC_DS13258,BMG_DS044182,"Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive"
+BMGC_DS13259,BMG_DS044184,"Hypokalemic Periodic Paralysis, Type 2"
+BMGC_DS13260,BMG_DS044185,Leber Congenital Amaurosis 14
+BMGC_DS13261,BMG_DS044186,"Retinal Dystrophy, Early-Onset Severe, Lrat-Related"
+BMGC_DS13262,BMG_DS044187,"RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED"
+BMGC_DS13263,BMG_DS044188,Spondylo-Megaepiphyseal-Metaphyseal Dysplasia
+BMGC_DS13264,BMG_DS044189,Plasminogen Activator Inhibitor-1 Deficiency
+BMGC_DS13265,BMG_DS044190,Roifman-Chitayat Syndrome
+BMGC_DS13266,BMG_DS044191,"Lipodystrophy, Congenital Generalized, Type 4"
+BMGC_DS13267,BMG_DS044192,Rhabdoid Tumor Predisposition Syndrome 2
+BMGC_DS13268,BMG_DS044193,"Chondrodysplasia, Megarbane-Dagher-Melki Type"
+BMGC_DS13269,BMG_DS044194,Miyoshi Muscular Dystrophy 3
+BMGC_DS13270,BMG_DS044195,Miyoshi Muscular Dystrophy 2
+BMGC_DS13271,BMG_DS044196,"Hypophosphatemic Rickets, Autosomal Recessive, 2"
+BMGC_DS13272,BMG_DS044197,Exudative Vitreoretinopathy 5
+BMGC_DS13273,BMG_DS044198,Diamond-Blackfan Anemia 10
+BMGC_DS13274,BMG_DS044199,Diamond-Blackfan Anemia 9
+BMGC_DS13275,BMG_DS044200,"Deafness, Autosomal Recessive 79"
+BMGC_DS13276,BMG_DS044201,"Bile Acid Malabsorption, Primary"
+BMGC_DS13277,BMG_DS044203,"Charcot-Marie-Tooth Disease, Axonal, Type 2n"
+BMGC_DS13278,BMG_DS044204,"Cardiomyopathy, Dilated, 1FF"
+BMGC_DS13279,BMG_DS044205,"herpes simplex encephalitis, susceptibility to, 1"
+BMGC_DS13280,BMG_DS044206,Karak Syndrome
+BMGC_DS13281,BMG_DS044207,"CEREBELLAR ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSEQUILIBRIUM SYNDROME 2"
+BMGC_DS13282,BMG_DS044208,Pitt-Hopkins-Like Syndrome 1
+BMGC_DS13283,BMG_DS044210,"Progeria Syndrome, Childhood-Onset"
+BMGC_DS13284,BMG_DS044211,Oculootodental syndrome
+BMGC_DS13285,BMG_DS044212,Omodysplasia 2
+BMGC_DS13286,BMG_DS044213,"Fibrosis of Extraocular Muscles, Congenital, 3C"
+BMGC_DS13287,BMG_DS044214,"Cap Myopathy, Tpm2-Related"
+BMGC_DS13288,BMG_DS044215,"Cap Myopathy, Tpm3-Related"
+BMGC_DS13289,BMG_DS044216,Bifid Nose With Or Without Anorectal And Renal Anomalies
+BMGC_DS13290,BMG_DS044217,NAFLD1
+BMGC_DS13291,BMG_DS044218,Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
+BMGC_DS13292,BMG_DS044220,"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6"
+BMGC_DS13293,BMG_DS044222,"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4"
+BMGC_DS13294,BMG_DS044223,"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3"
+BMGC_DS13295,BMG_DS044224,"Waardenburg Syndrome, Type 4c"
+BMGC_DS13296,BMG_DS044225,"Waardenburg Syndrome, Type 4b"
+BMGC_DS13297,BMG_DS044226,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 15"
+BMGC_DS13298,BMG_DS044227,"Cardiomyopathy, Dilated, 1EE"
+BMGC_DS13299,BMG_DS044228,"Cardiomyopathy, Familial Hypertrophic, 14"
+BMGC_DS13300,BMG_DS044229,"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 8"
+BMGC_DS13301,BMG_DS044230,"Cardiomyopathy, Familial Hypertrophic, 13"
+BMGC_DS13302,BMG_DS044231,"thyrotoxic periodic paralysis, susceptibility to, 2"
+BMGC_DS13303,BMG_DS044233,Focal Segmental Glomerulosclerosis 5
+BMGC_DS13304,BMG_DS044234,"factor XIII, b subunit, deficiency of"
+BMGC_DS13305,BMG_DS044235,"Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3"
+BMGC_DS13306,BMG_DS044236,"Factor Xiii, A Subunit, Deficiency Of"
+BMGC_DS13307,BMG_DS044237,"nasopharyngeal carcinoma, susceptibility to, 2"
+BMGC_DS13308,BMG_DS044238,Cone-Rod Dystrophy 13
+BMGC_DS13309,BMG_DS044239,"Amyotrophic Lateral Sclerosis 6, Autosomal Recessive"
+BMGC_DS13310,BMG_DS044240,Noonan Syndrome 6
+BMGC_DS13311,BMG_DS044241,"leprosy, susceptibility to, 5"
+BMGC_DS13312,BMG_DS044242,"DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL"
+BMGC_DS13313,BMG_DS044244,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C"
+BMGC_DS13314,BMG_DS044246,"Amelogenesis Imperfecta, Hypomaturation Type, Iia3"
+BMGC_DS13315,BMG_DS044248,"Spastic Paraplegia 44, Autosomal Recessive"
+BMGC_DS13316,BMG_DS044249,"Muscular Dystrophy, Congenital, Lmna-Related"
+BMGC_DS13317,BMG_DS044250,"Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency"
+BMGC_DS13318,BMG_DS044251,Weill-Marchesani-Like Syndrome
+BMGC_DS13319,BMG_DS044252,"Retinitis Pigmentosa, Concentric"
+BMGC_DS13320,BMG_DS044253,"CILIARY DYSKINESIA, PRIMARY, 13"
+BMGC_DS13321,BMG_DS044254,"intellectual disability, autosomal recessive 13"
+BMGC_DS13322,BMG_DS044255,Polymicrogyria With Optic Nerve Hypoplasia
+BMGC_DS13323,BMG_DS044256,"Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities"
+BMGC_DS13324,BMG_DS044257,Chromosome 5p13 Duplication Syndrome
+BMGC_DS13325,BMG_DS044258,Marie Unna Hereditary Hypotrichosis 1
+BMGC_DS13326,BMG_DS044259,Dystransthyretinemic Euthyroidal Hyperthyroxinemia
+BMGC_DS13327,BMG_DS044260,glioma susceptibility 1
+BMGC_DS13328,BMG_DS044261,"epilepsy, idiopathic generalized, susceptibility to, 9"
+BMGC_DS13329,BMG_DS044262,"epilepsy, juvenile myoclonic, susceptibility to, 6"
+BMGC_DS13330,BMG_DS044263,"epilepsy, juvenile absence, susceptibility to, 1"
+BMGC_DS13331,BMG_DS044264,"epilepsy, idiopathic generalized, susceptibility to, 11"
+BMGC_DS13332,BMG_DS044266,"Cardiomyopathy, Dilated, 1DD"
+BMGC_DS13333,BMG_DS044268,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 4"
+BMGC_DS13334,BMG_DS044269,"INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE"
+BMGC_DS13335,BMG_DS044271,"Choroidal Dystrophy, Central Areolar 3"
+BMGC_DS13336,BMG_DS044272,"Parkinsonism-Dystonia, Infantile"
+BMGC_DS13337,BMG_DS044274,Brugada Syndrome 8
+BMGC_DS13338,BMG_DS044275,"Cardiomyopathy, Dilated, 1CC"
+BMGC_DS13339,BMG_DS044276,Brugada Syndrome 7
+BMGC_DS13340,BMG_DS044277,Brugada Syndrome 6
+BMGC_DS13341,BMG_DS044278,Thrombophilia Due To Histidine-Rich Glycoprotein Deficiency
+BMGC_DS13342,BMG_DS044279,Thrombophilia Due To Elevated Histidine-Rich Glycoprotein
+BMGC_DS13343,BMG_DS044280,"Neuropathy, Hereditary Sensory And Autonomic, Type IIB"
+BMGC_DS13344,BMG_DS044281,"Fibrosis of Extraocular Muscles, Congenital, 3B"
+BMGC_DS13345,BMG_DS044284,"Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related"
+BMGC_DS13346,BMG_DS044285,Macrothrombocytopenia
+BMGC_DS13347,BMG_DS044286,"Neutropenia, Severe Congenital, Autosomal Dominant 2"
+BMGC_DS13348,BMG_DS044288,"CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2"
+BMGC_DS13349,BMG_DS044289,Hypotrichosis And Recurrent Skin Vesicles
+BMGC_DS13350,BMG_DS044290,familial hemophagocytic lymphohistiocytosis 5
+BMGC_DS13351,BMG_DS044291,"GLAUCOMA 1, OPEN ANGLE, O"
+BMGC_DS13352,BMG_DS044292,"melanoma, cutaneous malignant, susceptibility to, 5"
+BMGC_DS13353,BMG_DS044293,"INCREASED ANALGESIA FROM KAPPA-OPIOID RECEPTOR AGONIST, FEMALE-SPECIFIC"
+BMGC_DS13354,BMG_DS044294,"Tooth Agenesis, Selective, 6"
+BMGC_DS13355,BMG_DS044295,polycystic kidney disease 2
+BMGC_DS13356,BMG_DS044296,"Microphthalmia, Isolated 4"
+BMGC_DS13357,BMG_DS044297,Cone Dystrophy 4
+BMGC_DS13358,BMG_DS044298,Achromatopsia 5
+BMGC_DS13359,BMG_DS044299,"Hyperuricemic Nephropathy, Familial Juvenile 2"
+BMGC_DS13360,BMG_DS044301,CLAPO Syndrome
+BMGC_DS13361,BMG_DS044303,atrial septal defect 6
+BMGC_DS13362,BMG_DS044304,"Glaucoma 3, Primary Congenital, D"
+BMGC_DS13363,BMG_DS044305,"46, XY Sex Reversal 5"
+BMGC_DS13364,BMG_DS044306,Nijmegen Breakage Syndrome-Like Disorder
+BMGC_DS13365,BMG_DS044307,"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"
+BMGC_DS13367,BMG_DS044309,"Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis"
+BMGC_DS13368,BMG_DS044310,Metaphyseal Anadysplasia 2
+BMGC_DS13369,BMG_DS044311,BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3
+BMGC_DS13370,BMG_DS044312,"46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy"
+BMGC_DS13371,BMG_DS044313,"PULMONARY DISEASE, CHRONIC OBSTRUCTIVE, RATE OF DECLINE OF LUNG FUNCTION IN"
+BMGC_DS13372,BMG_DS044314,"cardiomyopathy, familial hypertrophic, 4, susceptibility to"
+BMGC_DS13373,BMG_DS044315,"CANDIDIASIS, FAMILIAL, 1"
+BMGC_DS13374,BMG_DS044316,Camptodactyly 1
+BMGC_DS13375,BMG_DS044317,"Bifid Nose, Autosomal Dominant"
+BMGC_DS13376,BMG_DS044318,"amyloidosis, hereditary systemic 1"
+BMGC_DS13377,BMG_DS044319,"Cerebral Amyloid Angiopathy, Gsn-Related"
+BMGC_DS13378,BMG_DS044320,"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT"
+BMGC_DS13379,BMG_DS044321,3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency
+BMGC_DS13380,BMG_DS044322,"Prostaglandin-Endoperoxide Synthase 1 Deficiency, Platelet"
+BMGC_DS13381,BMG_DS044323,"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED"
+BMGC_DS13382,BMG_DS044324,"basal cell carcinoma, susceptibility to, 1"
+BMGC_DS13383,BMG_DS044325,Neurodegeneration Due To Cerebral Folate Transport Deficiency
+BMGC_DS13384,BMG_DS044326,"leukemia, acute lymphocytic, susceptibility to, 2"
+BMGC_DS13385,BMG_DS044327,"leukemia, acute lymphocytic, susceptibility to, 1"
+BMGC_DS13386,BMG_DS044332,"epilepsy, idiopathic generalized, susceptibility to, 10"
+BMGC_DS13387,BMG_DS044335,"Atrial Fibrillation, Familial, 8"
+BMGC_DS13388,BMG_DS044336,"Pituitary Hormone Deficiency, Combined, 1"
+BMGC_DS13389,BMG_DS044338,Dursun Syndrome
+BMGC_DS13390,BMG_DS044343,glioma susceptibility 3
+BMGC_DS13391,BMG_DS044344,glioma susceptibility 2
+BMGC_DS13392,BMG_DS044345,Glycogen Storage Disease IXC
+BMGC_DS13393,BMG_DS044348,SCHIZOPHRENIA 13
+BMGC_DS13394,BMG_DS044349,"follicular lymphoma, susceptibility to, 1"
+BMGC_DS13395,BMG_DS044350,BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 2
+BMGC_DS13396,BMG_DS044354,"neuroblastoma, susceptibility to, 3"
+BMGC_DS13397,BMG_DS044355,"neuroblastoma, susceptibility to, 2"
+BMGC_DS13398,BMG_DS044357,"Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1"
+BMGC_DS13399,BMG_DS044361,Santos Syndrome
+BMGC_DS13400,BMG_DS044362,"epilepsy, idiopathic generalized, susceptibility to, 7"
+BMGC_DS13401,BMG_DS044363,"Febrile Convulsions, Familial, 3a"
+BMGC_DS13402,BMG_DS044364,"Retinitis Pigmentosa, Juvenile, Aipl1-Related"
+BMGC_DS13403,BMG_DS044365,"Cone-Rod Dystrophy, Aipl1-Related"
+BMGC_DS13404,BMG_DS044366,"Generalized Epilepsy With Febrile Seizures Plus, 7"
+BMGC_DS13405,BMG_DS044367,"Retinitis Pigmentosa, Juvenile, SPATA7-Related"
+BMGC_DS13406,BMG_DS044368,"attention deficit-hyperactivity disorder, susceptibility to, 7"
+BMGC_DS13407,BMG_DS044369,"IMMUNODEFICIENCY 83, SUSCEPTIBILITY TO VIRAL INFECTIONS"
+BMGC_DS13408,BMG_DS044370,"EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT"
+BMGC_DS13409,BMG_DS044371,Emery-Dreifuss Muscular Dystrophy 4
+BMGC_DS13410,BMG_DS044372,Spermatogenic Failure 7
+BMGC_DS13411,BMG_DS044373,Optic Atrophy 7
+BMGC_DS13412,BMG_DS044375,"Cataract, Autosomal Recessive Congenital 3"
+BMGC_DS13413,BMG_DS044376,"46, XY Disorders of Sex Development"
+BMGC_DS13414,BMG_DS044377,Premature Ovarian Failure 7
+BMGC_DS13415,BMG_DS044378,Multiple Synostoses Syndrome 3
+BMGC_DS13416,BMG_DS044379,"Ventricular Fibrillation, Paroxysmal Familial, 2"
+BMGC_DS13417,BMG_DS044380,Long Qt Syndrome 12
+BMGC_DS13418,BMG_DS044381,"Myopathy, Myofibrillar, Bag3-Related"
+BMGC_DS13419,BMG_DS044382,"PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE"
+BMGC_DS13420,BMG_DS044383,"Leukoencephalopathy, Cystic, Without Megalencephaly"
+BMGC_DS13421,BMG_DS044385,"Hypomyelination, Global Cerebral"
+BMGC_DS13422,BMG_DS044388,Hadziselimovic Syndrome
+BMGC_DS13423,BMG_DS044389,"Ventricular Fibrillation, Paroxysmal Familial, 1"
+BMGC_DS13424,BMG_DS044391,RETINITIS PIGMENTOSA 42
+BMGC_DS13425,BMG_DS044392,"Cutis Laxa, Autosomal Recessive, Type IIB"
+BMGC_DS13426,BMG_DS044393,"lethal polymalformative syndrome, Boissel type"
+BMGC_DS13427,BMG_DS044394,"Congenital Disorder of Glycosylation, Type Io"
+BMGC_DS13428,BMG_DS044395,"Spastic Paraplegia-50, Autosomal Recessive"
+BMGC_DS13429,BMG_DS044396,Glycogen Storage Disease XIV
+BMGC_DS13430,BMG_DS044397,Glycogen Storage Disease XIII
+BMGC_DS13431,BMG_DS044399,atypical hemolytic-uremic syndrome with thrombomodulin anomaly
+BMGC_DS13432,BMG_DS044400,atypical hemolytic-uremic syndrome with C3 anomaly
+BMGC_DS13433,BMG_DS044401,atypical hemolytic-uremic syndrome with B factor anomaly
+BMGC_DS13434,BMG_DS044402,atypical hemolytic-uremic syndrome with I factor anomaly
+BMGC_DS13435,BMG_DS044403,atypical hemolytic-uremic syndrome with MCP/CD46 anomaly
+BMGC_DS13436,BMG_DS044404,Three M Syndrome 2
+BMGC_DS13437,BMG_DS044405,"Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi"
+BMGC_DS13438,BMG_DS044406,Giacheti Syndrome
+BMGC_DS13439,BMG_DS044407,Zechi-Ceide Syndrome
+BMGC_DS13440,BMG_DS044408,Orofaciodigital syndrome 11
+BMGC_DS13441,BMG_DS044410,"Cerebral Palsy, Spastic Quadriplegic, 2"
+BMGC_DS13442,BMG_DS044411,"epilepsy, idiopathic generalized, susceptibility to, 8"
+BMGC_DS13443,BMG_DS044412,"Heterotopia, Periventricular, Associated With Chromosome 5q Deletion"
+BMGC_DS13444,BMG_DS044413,"Cardiomyopathy, Dilated, 1BB"
+BMGC_DS13445,BMG_DS044414,Erythrocyte Amp Deaminase Deficiency
+BMGC_DS13446,BMG_DS044415,ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY
+BMGC_DS13447,BMG_DS044416,ALPHA-2-PLASMIN INHIBITOR DEFICIENCY
+BMGC_DS13448,BMG_DS044417,"Neuropathy, Hereditary Sensory And Autonomic, Type IIA"
+BMGC_DS13449,BMG_DS044418,"pelvic organ prolapse, susceptibility to"
+BMGC_DS13450,BMG_DS044419,"XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C"
+BMGC_DS13451,BMG_DS044420,"46,XY sex reversal 4"
+BMGC_DS13452,BMG_DS044421,malposition of teeth with or without hypodontia/oligodontia
+BMGC_DS13453,BMG_DS044423,acute myeloid leukemia with myelodysplasia-related changes
+BMGC_DS13454,BMG_DS044424,myeloid leukemia associated with down syndrome
+BMGC_DS13455,BMG_DS044428,mixed phenotype acute leukemia with t(v;11q23.3)
+BMGC_DS13456,BMG_DS044429,acute myeloid leukemia with t(6;9) (p23;q34.1)
+BMGC_DS13457,BMG_DS044430,acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2)
+BMGC_DS13458,BMG_DS044431,acute myeloid leukemia with mutated NPM1
+BMGC_DS13459,BMG_DS044439,"SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE"
+BMGC_DS13460,BMG_DS044440,"DEAFNESS, AUTOSOMAL RECESSIVE 86"
+BMGC_DS13461,BMG_DS044441,"DEAFNESS, AUTOSOMAL RECESSIVE 88"
+BMGC_DS13462,BMG_DS044476,Infection due to Opisthorchis (felineus)(viverrini)
+BMGC_DS13463,BMG_DS044477,Infection due to cat liver fluke
+BMGC_DS13464,BMG_DS044573,Adenomatosis of colon
+BMGC_DS13465,BMG_DS044592,Other aplastic anemias and other bone marrow failure syndromes
+BMGC_DS13466,BMG_DS044606,Bernard-Soulier [giant platelet] syndrome
+BMGC_DS13467,BMG_DS044607,Thromboasthenia (hemorrhagic) (hereditary)
+BMGC_DS13468,BMG_DS044610,Cell membrane receptor complex [CR3] defect
+BMGC_DS13469,BMG_DS044616,Other and unspecified diseases of blood and blood-forming organs
+BMGC_DS13470,BMG_DS044617,Polycythemia due to erythropoietin
+BMGC_DS13471,BMG_DS044618,Polycythemia due to stress
+BMGC_DS13472,BMG_DS044627,C1 esterase inhibitor [C1-INH] deficiency
+BMGC_DS13473,BMG_DS044770,Isolated pituitary hormone deficiency
+BMGC_DS13474,BMG_DS044771,Pituitary short stature
+BMGC_DS13475,BMG_DS044780,"DELAYED PUBERTY, SELF-LIMITED"
+BMGC_DS13476,BMG_DS044786,Beriberi with cardiovascular manifestations
+BMGC_DS13477,BMG_DS044787,Shoshin disease
+BMGC_DS13478,BMG_DS044823,"GM2-GANGLIOSIDOSIS, ADULT"
+BMGC_DS13479,BMG_DS044853,Other and unspecified metabolic disorders
+BMGC_DS13480,BMG_DS044890,Familial torsion dystonia
+BMGC_DS13481,BMG_DS044895,Disseminated multiple sclerosis
+BMGC_DS13482,BMG_DS044936,Epilepsies and epileptic syndromes undetermined as to whether they are focal or generalized
+BMGC_DS13483,BMG_DS045055,Peroneal muscular atrophy (axonal type) (hypertrophic type)
+BMGC_DS13484,BMG_DS045056,Dominantly inherited sensory neuropathy
+BMGC_DS13485,BMG_DS045057,Nelaton's syndrome
+BMGC_DS13486,BMG_DS045058,Recessively inherited sensory neuropathy
+BMGC_DS13487,BMG_DS045074,Paraplegia (paraparesis) and quadriplegia (quadriparesis)
+BMGC_DS13488,BMG_DS047090,"Cardiac, heart or myocardial failure NOS"
+BMGC_DS13489,BMG_DS047560,Sepsis caused by Streptococcus pneumoniae
+BMGC_DS13490,BMG_DS047563,Sepsis caused by Staphylococcus aureus
+BMGC_DS13491,BMG_DS047566,Sepsis caused by Haemophilus influenzae
+BMGC_DS13492,BMG_DS047570,Sepsis due to Pseudomonas
+BMGC_DS13493,BMG_DS047571,Sepsis caused by Serratia
+BMGC_DS13494,BMG_DS047776,Bronchopneumonia due to S. pneumoniae
+BMGC_DS13495,BMG_DS047813,"Respiratory Distress Syndrome, Acute"
+BMGC_DS13496,BMG_DS047847,Dental abscess with sinus
+BMGC_DS13497,BMG_DS047848,Dentoalveolar abscess with sinus
+BMGC_DS13498,BMG_DS047959,Crohn's disease [regional enteritis] of duodenum
+BMGC_DS13499,BMG_DS047960,Crohn's disease [regional enteritis] of ileum
+BMGC_DS13500,BMG_DS047961,Crohn's disease [regional enteritis] of jejunum
+BMGC_DS13501,BMG_DS048230,Psoriasiform diaper rash
+BMGC_DS13502,BMG_DS048235,Other and unspecified dermatitis
+BMGC_DS13503,BMG_DS048236,Von Zumbusch's disease
+BMGC_DS13504,BMG_DS048618,Atrophie blanche (en plaque)
+BMGC_DS13505,BMG_DS049585,Post traumatic osteoarthritis
+BMGC_DS13506,BMG_DS050995,"Other and unspecified soft tissue disorders, not elsewhere classified"
+BMGC_DS13507,BMG_DS051828,Nephrotic syndrome with focal and segmental hyalinosis
+BMGC_DS13508,BMG_DS051829,Nephrotic syndrome with focal and segmental sclerosis
+BMGC_DS13509,BMG_DS051830,Nephrotic syndrome with focal glomerulonephritis
+BMGC_DS13510,BMG_DS051896,Other and unspecified disorders of prostate
+BMGC_DS13511,BMG_DS052027,twin to twin transfusion syndrome
+BMGC_DS13512,BMG_DS052107,Congenital cerebral aneurysm (nonruptured)
+BMGC_DS13513,BMG_DS052120,Hemimelia of limb NOS
+BMGC_DS13514,BMG_DS052121,Asphyxiating thoracic dysplasia [Jeune]
+BMGC_DS13515,BMG_DS052123,Inherited keratosis palmaris et plantaris
+BMGC_DS13516,BMG_DS052124,Keratosis follicularis [Darier-White]
+BMGC_DS13517,BMG_DS052131,Trisomy 18 and Trisomy 13
+BMGC_DS13518,BMG_DS052138,"46, XY with streak gonads"
+BMGC_DS13519,BMG_DS052232,Congenital hemolytic uremic syndrome
+BMGC_DS13520,BMG_DS052236,Nonsustained Ventricular Tachycardia
+BMGC_DS13521,BMG_DS052256,acute myeloid leukemia with t(9;11)(p22;q23)
+BMGC_DS13522,BMG_DS052268,Glycogen storage disease type Ia
+BMGC_DS13523,BMG_DS052277,Chronic ulcerative colitis
+BMGC_DS13524,BMG_DS052293,cerebral cavernous malformation
+BMGC_DS13525,BMG_DS052318,Bilateral Wilms Tumor
+BMGC_DS13526,BMG_DS052322,Pulmonary Fibrosis - from Asbestos Exposure
+BMGC_DS13527,BMG_DS052323,Sex Differentiation Disorders
+BMGC_DS13528,BMG_DS052327,Familial acanthosis nigricans
+BMGC_DS13529,BMG_DS052330,Primary visual agnosia
+BMGC_DS13530,BMG_DS052335,Familial antiphospholipid syndrome
+BMGC_DS13531,BMG_DS052365,Familial pityriasis rubra pilaris
+BMGC_DS13532,BMG_DS052366,Idiopathic intracranial hypertension with papilledema
+BMGC_DS13533,BMG_DS052367,Hypopituitarism and septooptic 'dysplasia'
+BMGC_DS13534,BMG_DS052378,"Premature ovarian failure, familial"
+BMGC_DS13535,BMG_DS052382,Ramer Ladda syndrome
+BMGC_DS13536,BMG_DS052383,Ramos Arroyo Clark syndrome
+BMGC_DS13537,BMG_DS052394,"Cataract, congenital, with microcornea or slight microphthalmia"
+BMGC_DS13538,BMG_DS052404,"Congenital thrombotic disease, due to Protein C deficiency"
+BMGC_DS13539,BMG_DS052406,Benign essential blepharospasm
+BMGC_DS13540,BMG_DS052408,Beta-sarcoglycanopathy
+BMGC_DS13541,BMG_DS052417,Ring Chromosome 14 Syndrome
+BMGC_DS13542,BMG_DS052427,Abdominal obesity metabolic syndrome
+BMGC_DS13543,BMG_DS052448,Freire-Maia odontotrichomelic syndrome
+BMGC_DS13544,BMG_DS052449,Frenkel Russe syndrome
+BMGC_DS13545,BMG_DS052455,"digestive system neuroendocrine tumor, grade 1/2"
+BMGC_DS13546,BMG_DS052458,Acromesomelic dysplasia Hunter-Thompson type
+BMGC_DS13547,BMG_DS052462,Acute erythroleukemia
+BMGC_DS13548,BMG_DS052463,Acute erythroleukemia - M6a subtype
+BMGC_DS13549,BMG_DS052464,Acute myeloid leukemia FAB-M6
+BMGC_DS13550,BMG_DS052465,Acute erythroleukemia - M6b subtype
+BMGC_DS13551,BMG_DS052466,Richieri Costa Da Silva syndrome
+BMGC_DS13552,BMG_DS052468,"malignant hyperthermia, susceptibility to, 1"
+BMGC_DS13553,BMG_DS052469,"malignant hyperthermia, susceptibility to, 2"
+BMGC_DS13554,BMG_DS052470,"malignant hyperthermia, susceptibility to, 3"
+BMGC_DS13555,BMG_DS052472,"Maple syrup urine disease, type 1A"
+BMGC_DS13556,BMG_DS052473,"Maple syrup urine disease, type 1B"
+BMGC_DS13557,BMG_DS052476,Familial duodenal atresia
+BMGC_DS13558,BMG_DS052477,Dyschromatosis universalis hereditaria
+BMGC_DS13559,BMG_DS052479,Congenital disorder of glycosylation type 1C
+BMGC_DS13560,BMG_DS052480,Congenital disorder of glycosylation type 1G
+BMGC_DS13561,BMG_DS052481,Congenital disorder of glycosylation type 1H
+BMGC_DS13562,BMG_DS052482,Congenital disorder of glycosylation type 1J
+BMGC_DS13563,BMG_DS052483,Congenital disorder of glycosylation type 1K
+BMGC_DS13564,BMG_DS052484,Congenital disorder of glycosylation type 1L
+BMGC_DS13565,BMG_DS052485,Congenital disorder of glycosylation type 1X
+BMGC_DS13566,BMG_DS052486,Congenital disorder of glycosylation type 2A
+BMGC_DS13567,BMG_DS052487,Congenital disorder of glycosylation type 2D
+BMGC_DS13568,BMG_DS052488,Congenital disorder of glycosylation type 2E
+BMGC_DS13569,BMG_DS052489,"Congenital disorder of glycosylation, type 2G"
+BMGC_DS13570,BMG_DS052491,"Cystinosis, benign, nonnephropathic"
+BMGC_DS13571,BMG_DS052496,split hand-foot malformation 1
+BMGC_DS13572,BMG_DS052505,"Nevi flammei, familial multiple"
+BMGC_DS13573,BMG_DS052511,"Pulmonary alveolar proteinosis, congenital"
+BMGC_DS13574,BMG_DS052513,"Pancreatic cancer, adult"
+BMGC_DS13575,BMG_DS052514,familial pancreatic carcinoma
+BMGC_DS13576,BMG_DS052517,Hawkinsinuria
+BMGC_DS13577,BMG_DS052519,"Heart defect, tongue hamartoma and polysyndactyly"
+BMGC_DS13578,BMG_DS052521,HEM dysplasia
+BMGC_DS13579,BMG_DS052525,Rubinstein Taybi like syndrome
+BMGC_DS13580,BMG_DS052526,Rudd Klimek syndrome
+BMGC_DS13581,BMG_DS052531,Marfan Syndrome Type 2
+BMGC_DS13582,BMG_DS052532,Marie Unna congenital hypotrichosis
+BMGC_DS13583,BMG_DS052533,Mononen Karnes Senac syndrome
+BMGC_DS13584,BMG_DS052537,Pierre Robin Sequence with Facial and Digital Anomalies
+BMGC_DS13585,BMG_DS052540,"Cholestasis, progressive familial intrahepatic 4"
+BMGC_DS13586,BMG_DS052544,Epidermolysa bullosa simplex and limb girdle muscular dystrophy
+BMGC_DS13587,BMG_DS052545,"Collagenopathy, type 2 alpha 1"
+BMGC_DS13588,BMG_DS052553,Familial apoceruloplasmin deficiency
+BMGC_DS13589,BMG_DS052562,Maternally Inherited Leigh Syndrome
+BMGC_DS13590,BMG_DS052563,"Osteogenesis Imperfecta, Type V"
+BMGC_DS13591,BMG_DS052570,Hydrolethalus syndrome
+BMGC_DS13592,BMG_DS052571,"Hypercalciuria, childhood idiopathic"
+BMGC_DS13593,BMG_DS052573,"Myasthenic syndrome, congenital, postsynaptic slow-channel"
+BMGC_DS13594,BMG_DS052577,"Myopia, susceptibility to"
+BMGC_DS13595,BMG_DS052578,myostatin-related muscle hypertrophy
+BMGC_DS13596,BMG_DS052582,Cerebral Nocardiosis
+BMGC_DS13597,BMG_DS052583,Fetal megacystis
+BMGC_DS13598,BMG_DS052584,Megalocytic interstitial nephritis
+BMGC_DS13599,BMG_DS052587,Meier Blumberg Imahorn syndrome
+BMGC_DS13600,BMG_DS052588,Keratosis palmoplantaris striata 1
+BMGC_DS13601,BMG_DS052589,Keratosis palmoplantaris striata 3
+BMGC_DS13602,BMG_DS052596,Clark-Baraitser syndrome
+BMGC_DS13603,BMG_DS052597,"Crigler Najjar syndrome, type 2"
+BMGC_DS13604,BMG_DS052598,Pediatric Crohn's disease
+BMGC_DS13605,BMG_DS052599,"Cutis laxa, recessive"
+BMGC_DS13606,BMG_DS052600,Blepharophimosis syndrome type 1
+BMGC_DS13607,BMG_DS052601,Blepharophimosis syndrome type 2
+BMGC_DS13608,BMG_DS052605,Nonkeratan-sulfate-excreting Morquio syndrome
+BMGC_DS13609,BMG_DS052607,Qazi Markouizos syndrome
+BMGC_DS13610,BMG_DS052611,Radio renal syndrome
+BMGC_DS13611,BMG_DS052618,Immunoglobulin a deficiency 1
+BMGC_DS13612,BMG_DS052626,Juvenile pauciarticular chronic arthritis
+BMGC_DS13613,BMG_DS052630,"Vestibulocochlear Dysfunction, Progressive"
+BMGC_DS13614,BMG_DS052633,Angiofollicular ganglionic hyperplasia
+BMGC_DS13615,BMG_DS052634,Abdominal angiostrongyliasis
+BMGC_DS13616,BMG_DS052635,Intravitreal angiostrongyliasis
+BMGC_DS13617,BMG_DS052641,Nephropathic cystinosis
+BMGC_DS13618,BMG_DS052645,Prinzmetal's variant angina
+BMGC_DS13619,BMG_DS052651,bladder urachal carcinoma
+BMGC_DS13620,BMG_DS052653,"Usher syndrome, type 1B"
+BMGC_DS13621,BMG_DS052654,"Usher syndrome, type 1C"
+BMGC_DS13622,BMG_DS052655,"Usher syndrome, type 1D"
+BMGC_DS13623,BMG_DS052657,"Usher syndrome, type 1F"
+BMGC_DS13624,BMG_DS052659,"Usher syndrome, type 2C"
+BMGC_DS13625,BMG_DS052660,Tetra amelia with ectodermal dysplasia and lacrimal duct abnormalities
+BMGC_DS13626,BMG_DS052664,Tetraamelia multiple malformations
+BMGC_DS13627,BMG_DS052669,6 alpha mercaptopurine sensitivity
+BMGC_DS13628,BMG_DS052674,"VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS"
+BMGC_DS13629,BMG_DS052675,Vacuolar myopathy
+BMGC_DS13630,BMG_DS052682,"triphalangeal thumb, Nonopposable"
+BMGC_DS13631,BMG_DS052685,Waldmann disease
+BMGC_DS13632,BMG_DS052688,"Craniometaphyseal dysplasia, autosomal recessive type"
+BMGC_DS13633,BMG_DS052689,Bone Marrow Failure Disorders
+BMGC_DS13634,BMG_DS052690,Potocki-Lupski syndrome
+BMGC_DS13635,BMG_DS052691,"Chromosome 18, monosomy 18Q"
+BMGC_DS13636,BMG_DS052695,"Alport syndrome, dominant type"
+BMGC_DS13637,BMG_DS052696,"Alport syndrome, recessive type"
+BMGC_DS13638,BMG_DS052699,"Amaurosis congenita of Leber, type 1"
+BMGC_DS13639,BMG_DS052701,famililal cerebral cavernous malformations
+BMGC_DS13640,BMG_DS052704,Scapuloperoneal myopathy
+BMGC_DS13641,BMG_DS052711,Spastic paraplegia 17
+BMGC_DS13642,BMG_DS052714,Perniola Krajewska Carnevale syndrome
+BMGC_DS13643,BMG_DS052722,"Welander distal myopathy, Swedish type"
+BMGC_DS13644,BMG_DS052723,Wells Jankovic syndrome
+BMGC_DS13645,BMG_DS052728,Yorifuji Okuno syndrome
+BMGC_DS13646,BMG_DS052731,Combined immunodeficiency due to ZAP70 deficiency
+BMGC_DS13647,BMG_DS052736,Woods Leversha Rogers syndrome
+BMGC_DS13648,BMG_DS052744,T cell immunodeficiency primary
+BMGC_DS13649,BMG_DS052754,Glucose-6-phosphate translocase deficiency
+BMGC_DS13650,BMG_DS052757,Familial myelofibrosis
+BMGC_DS13651,BMG_DS052760,"Spastic paraplegia 3, autosomal dominant"
+BMGC_DS13652,BMG_DS052783,Moyamoya disease 1
+BMGC_DS13653,BMG_DS052793,"Bulbospinal neuronopathy, X-linked recessive"
+BMGC_DS13654,BMG_DS052798,Familial lipomyelomeningocele
+BMGC_DS13655,BMG_DS052799,Long QT syndrome type 3
+BMGC_DS13656,BMG_DS052813,Bare lymphocyte syndrome 2
+BMGC_DS13657,BMG_DS052815,Brachydactylous dwarfism Mseleni type
+BMGC_DS13658,BMG_DS052819,Orofaciodigital syndrome type1
+BMGC_DS13659,BMG_DS052825,Paraquat lung
+BMGC_DS13660,BMG_DS052831,"Hereditary spastic paralysis, infantile onset ascending"
+BMGC_DS13661,BMG_DS052845,"Prosopagnosia, hereditary"
+BMGC_DS13662,BMG_DS052846,"prostate cancer, hereditary"
+BMGC_DS13663,BMG_DS052848,Lynch syndrome I (site-specific colonic cancer)
+BMGC_DS13664,BMG_DS052850,Forney Robinson Pascoe syndrome
+BMGC_DS13665,BMG_DS052853,Goldblatt Viljoen syndrome
+BMGC_DS13666,BMG_DS052865,Multiple system atrophy (MSA) with orthostatic hypotension
+BMGC_DS13667,BMG_DS052867,"Neurofibromatosis, Type 3, mixed central and peripheral"
+BMGC_DS13668,BMG_DS052869,Neurofibromatosis-Noonan syndrome
+BMGC_DS13669,BMG_DS052875,Zlotogora-Ogur syndrome
+BMGC_DS13670,BMG_DS052882,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 1"
+BMGC_DS13671,BMG_DS052884,Microphthalmia and mental deficiency
+BMGC_DS13672,BMG_DS052886,"Microtia, meatal atresia and conductive deafness"
+BMGC_DS13673,BMG_DS052942,deletion 5q35
+BMGC_DS13674,BMG_DS052943,Basaran Yilmaz syndrome
+BMGC_DS13675,BMG_DS052949,Gaucher-like disease
+BMGC_DS13676,BMG_DS052980,"Chromosome 8, monosomy 8p23 1"
+BMGC_DS13677,BMG_DS052984,O'Donnell Pappas syndrome
+BMGC_DS13678,BMG_DS052987,Laplane Fontaine Lagardere syndrome
+BMGC_DS13679,BMG_DS052988,"Larsen syndrome, dominant type"
+BMGC_DS13680,BMG_DS052996,Phacomatosis pigmentokeratotica
+BMGC_DS13681,BMG_DS053000,Baraitser Brett Piesowicz syndrome
+BMGC_DS13682,BMG_DS053007,"Cerebral hemorrhage with amyloidosis, hereditary, Dutch type"
+BMGC_DS13683,BMG_DS053008,"Ceroid lipofuscinosis, neuronal 1, infantile"
+BMGC_DS13684,BMG_DS053015,"Camurati Engelmann disease, type 2"
+BMGC_DS13685,BMG_DS053018,"Charcot-Marie-Tooth disease, Type 1E"
+BMGC_DS13686,BMG_DS053019,Dysferlinopathy
+BMGC_DS13687,BMG_DS053020,myotonic dystrophy type 2
+BMGC_DS13688,BMG_DS053031,"Deafness, autosomal dominant nonsyndromic sensorineural 17"
+BMGC_DS13689,BMG_DS053035,Fronto-facio-nasal dysplasia
+BMGC_DS13690,BMG_DS053050,Lactate dehydrogenase deficiency type A
+BMGC_DS13691,BMG_DS053053,Sulfocysteinuria
+BMGC_DS13692,BMG_DS053062,Acquired angioedema
+BMGC_DS13693,BMG_DS053066,Acrofacial dysostosis Catania form
+BMGC_DS13694,BMG_DS053071,"Deafness, autosomal dominant nonsyndromic sensorineural 22"
+BMGC_DS13695,BMG_DS053082,Adenosine monophosphate deaminase deficiency
+BMGC_DS13696,BMG_DS053083,Amelogenesis imperfecta nephrocalcinosis
+BMGC_DS13697,BMG_DS053084,Amyloid angiopathy
+BMGC_DS13698,BMG_DS053085,"Amyotrophic lateral sclerosis, type 6"
+BMGC_DS13699,BMG_DS053086,familial atrial myxoma
+BMGC_DS13700,BMG_DS053087,Atypical Hemolytic Uremic Syndrome
+BMGC_DS13701,BMG_DS053098,2q24 microdeletion syndrome
+BMGC_DS13702,BMG_DS053099,Chromosome 2q37 deletion syndrome
+BMGC_DS13703,BMG_DS053103,Nakamura Osame syndrome
+BMGC_DS13704,BMG_DS053104,nasopharyngeal carcinoma
+BMGC_DS13705,BMG_DS053108,Potassium aggravated myotonia
+BMGC_DS13706,BMG_DS053112,MacKay Shek Carr syndrome
+BMGC_DS13707,BMG_DS053113,"hyperinsulinemic hypoglycemia, familial, 1"
+BMGC_DS13708,BMG_DS053114,"hyperinsulinemic hypoglycemia, familial, 2"
+BMGC_DS13709,BMG_DS053115,Hyperprolinemia type 2
+BMGC_DS13710,BMG_DS053116,Familial hypertryptophanemia
+BMGC_DS13711,BMG_DS053117,Familial HDL deficiency
+BMGC_DS13712,BMG_DS053121,Spinal muscular atrophy 4
+BMGC_DS13713,BMG_DS053122,Neurodegeneration with brain iron accumulation (NBIA)
+BMGC_DS13714,BMG_DS053127,Aase Smith syndrome 2
+BMGC_DS13715,BMG_DS053138,Familial schizencephaly
+BMGC_DS13716,BMG_DS053140,Free sialic acid storage disease
+BMGC_DS13717,BMG_DS053143,Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells
+BMGC_DS13718,BMG_DS053149,"Reticuloendotheliosis, familial, with eosinophilia"
+BMGC_DS13719,BMG_DS053152,Pfeiffer type acrocephalosyndactyly
+BMGC_DS13720,BMG_DS053155,"Necrotizing encephalopathy, infantile subacute, of Leigh"
+BMGC_DS13721,BMG_DS053163,Limb-girdle muscular dystrophy autosomal recessive
+BMGC_DS13722,BMG_DS053175,Hyperkeratosis of the palms and soles and esophageal papillomas
+BMGC_DS13723,BMG_DS053178,Mitochondrial cytopathy
+BMGC_DS13724,BMG_DS053182,Gestational Diabetes Insipidus
+BMGC_DS13725,BMG_DS053184,Inherited Peripheral Neuropathy
+BMGC_DS13726,BMG_DS053187,Pontocerebellar Hypoplasia Type 2
+BMGC_DS13727,BMG_DS053188,Pseudohypoparathyroidism Type 1C
+BMGC_DS13728,BMG_DS053189,Pseudohypoparathyroidism Type 2
+BMGC_DS13729,BMG_DS053199,Sarcoglycanopathies
+BMGC_DS13730,BMG_DS053200,Alpha-Sarcoglycanopathies
+BMGC_DS13731,BMG_DS053201,22q11 Deletion Syndrome
+BMGC_DS13732,BMG_DS053202,"46, XX Disorders of Sex Development"
+BMGC_DS13733,BMG_DS053203,alpha-Dystroglycanopathies
+BMGC_DS13734,BMG_DS053204,"46, XX Testicular Disorders of Sex Development"
+BMGC_DS13735,BMG_DS053207,Pyogenic Sacroiliitis
+BMGC_DS13736,BMG_DS053208,Septic Sacroiliitis
+BMGC_DS13737,BMG_DS053210,Chronic Liver Failure
+BMGC_DS13738,BMG_DS053211,Familial CHARGE Syndrome
+BMGC_DS13739,BMG_DS053215,Acquired Hypogammaglobulinemia
+BMGC_DS13740,BMG_DS053216,"Immunoglobulin Deficiency, Late-Onset"
+BMGC_DS13741,BMG_DS053217,Swyer Syndrome
+BMGC_DS13742,BMG_DS053219,Familial Kleine-Levin Syndrome
+BMGC_DS13743,BMG_DS053220,"Hyper-Immunoglobulin E Syndrome, Autosomal Dominant"
+BMGC_DS13744,BMG_DS053221,"48,XXYY Syndrome"
+BMGC_DS13745,BMG_DS053223,lymphoplasmacytic lymphoma
+BMGC_DS13746,BMG_DS053224,Nevo syndrome
+BMGC_DS13747,BMG_DS053226,Hydroxymethylbilane Synthase Deficiency
+BMGC_DS13748,BMG_DS053227,Generalized Myotonia of Thomsen
+BMGC_DS13749,BMG_DS053228,Lynch syndrome 1
+BMGC_DS13750,BMG_DS053229,"Antley-Bixler Syndrome, Autosomal Dominant"
+BMGC_DS13751,BMG_DS053230,Spinocerebellar ataxia 30
+BMGC_DS13752,BMG_DS053232,fumarase deficiency
+BMGC_DS13753,BMG_DS053233,Focal facial dermal dysplasia
+BMGC_DS13754,BMG_DS053234,Keratosis of Greither
+BMGC_DS13755,BMG_DS053238,Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
+BMGC_DS13756,BMG_DS053239,N syndrome
+BMGC_DS13757,BMG_DS053240,"Spastic paraplegia 25, autosomal recessive"
+BMGC_DS13758,BMG_DS053241,Bardet-Biedl syndrome 1
+BMGC_DS13759,BMG_DS053242,Bardet-Biedl syndrome 2
+BMGC_DS13760,BMG_DS053243,Bardet-Biedl syndrome 4
+BMGC_DS13761,BMG_DS053245,"SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT"
+BMGC_DS13762,BMG_DS053246,"Spastic Paraplegia 37, Autosomal Dominant"
+BMGC_DS13763,BMG_DS053250,"Opitz GBBB Syndrome, X-Linked"
+BMGC_DS13764,BMG_DS053252,Cross syndrome
+BMGC_DS13765,BMG_DS053259,Chronic ulcerative proctitis
+BMGC_DS13766,BMG_DS053262,Biotin deficiency disease
+BMGC_DS13767,BMG_DS053267,spinal cord glioma
+BMGC_DS13768,BMG_DS053273,"THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT"
+BMGC_DS13769,BMG_DS053274,Congenital hereditary muscular dystrophy
+BMGC_DS13770,BMG_DS053275,intracerebral hemorrhage
+BMGC_DS13771,BMG_DS053276,Recurrent aphthous ulcer
+BMGC_DS13772,BMG_DS053293,Meconium ileus
+BMGC_DS13773,BMG_DS053310,myeloid neoplasm
+BMGC_DS13774,BMG_DS053311,Deficiency of glucose-6-phosphate dehydrogenase
+BMGC_DS13775,BMG_DS053315,Thyroid Hormone Resistance Syndrome
+BMGC_DS13776,BMG_DS053327,Limb ischemia
+BMGC_DS13777,BMG_DS053347,Infection caused by carbapenem resistant Acinetobacter
+BMGC_DS13778,BMG_DS053390,Fungal septicemia
+BMGC_DS13779,BMG_DS053397,Hemoglobin H constant spring thalassemia
+BMGC_DS13780,BMG_DS053408,alveolar capillary dysplasia with misalignment of pulmonary veins
+BMGC_DS13781,BMG_DS053436,Dentinogenesis imperfecta without osteogenesis imperfecta
+BMGC_DS13782,BMG_DS053439,Pulmonary arterial hypertension
+BMGC_DS13783,BMG_DS053440,Coxiella burnetii Infection
+BMGC_DS13784,BMG_DS053519,Superficial mycosis
+BMGC_DS13785,BMG_DS053524,Glaucoma of childhood
+BMGC_DS13786,BMG_DS053526,cleft palate
+BMGC_DS13787,BMG_DS053531,papillary tumor of the pineal region
+BMGC_DS13788,BMG_DS053532,Fetal Alcohol Spectrum Disorders
+BMGC_DS13789,BMG_DS053533,Rhabdoid tumor predisposition syndrome
+BMGC_DS13790,BMG_DS053539,diffuse intrinsic pontine glioma
+BMGC_DS13791,BMG_DS053540,Congenital Bone Marrow Failure Syndromes
+BMGC_DS13792,BMG_DS053541,overgrowth syndrome
+BMGC_DS13793,BMG_DS053551,alcohol-related birth defect
+BMGC_DS13794,BMG_DS053552,"DEAFNESS, AUTOSOMAL RECESSIVE 76"
+BMGC_DS13795,BMG_DS053553,"DEAFNESS, AUTOSOMAL DOMINANT, WITH PERIPHERAL NEUROPATHY"
+BMGC_DS13796,BMG_DS053554,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E"
+BMGC_DS13797,BMG_DS053555,"WOOLLY HAIR, AUTOSOMAL RECESSIVE 2, WITH OR WITHOUT HYPOTRICHOSIS"
+BMGC_DS13798,BMG_DS053556,WH/HT
+BMGC_DS13799,BMG_DS053557,"FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED"
+BMGC_DS13800,BMG_DS053558,"USHER SYNDROME, TYPE IIC, GPR98/PDZD7 DIGENIC"
+BMGC_DS13801,BMG_DS053560,"DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOPATHY"
+BMGC_DS13802,BMG_DS053561,"SEIZURES, BENIGN FAMILIAL NEONATAL, 1"
+BMGC_DS13803,BMG_DS053562,"SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA"
+BMGC_DS13804,BMG_DS053563,"GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE"
+BMGC_DS13805,BMG_DS053564,"PARASOMNIA, SLEEPTALKING TYPE"
+BMGC_DS13806,BMG_DS053567,"CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KB"
+BMGC_DS13807,BMG_DS053568,"IMMUNODEFICIENCY, COMMON VARIABLE, 1"
+BMGC_DS13808,BMG_DS053569,"DERMATOFIBROSIS LENTICULARIS DISSEMINATA, ISOLATED"
+BMGC_DS13809,BMG_DS053570,HYPERALPHALIPOPROTEINEMIA 1
+BMGC_DS13810,BMG_DS053571,keloid formation
+BMGC_DS13811,BMG_DS053572,"LARYNGOSPASM, SEVERE NEONATAL EPISODIC"
+BMGC_DS13812,BMG_DS053574,"DEAFNESS, AUTOSOMAL DOMINANT, WITHOUT VESTIBULAR INVOLVEMENT"
+BMGC_DS13813,BMG_DS053575,"MELORHEOSTOSIS, ISOLATED"
+BMGC_DS13814,BMG_DS053577,Melorheostosis with Osteopoikilosis
+BMGC_DS13815,BMG_DS053579,MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)
+BMGC_DS13816,BMG_DS053580,CHROMOSOME 7q11.23 TRIPLICATION SYNDROME
+BMGC_DS13817,BMG_DS053582,POLYCYSTIC KIDNEY DISEASE 1
+BMGC_DS13818,BMG_DS053583,"amyotrophic lateral sclerosis, susceptibility to, 13"
+BMGC_DS13819,BMG_DS053585,"PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL"
+BMGC_DS13820,BMG_DS053586,ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS
+BMGC_DS13821,BMG_DS053587,BARDET-BIEDL SYNDROME 15
+BMGC_DS13822,BMG_DS053588,"CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB"
+BMGC_DS13823,BMG_DS053589,"IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS"
+BMGC_DS13824,BMG_DS053590,"FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, TARDBP-RELATED"
+BMGC_DS13825,BMG_DS053591,"FTLD-TDP, TARDBP-RELATED"
+BMGC_DS13826,BMG_DS053592,MITOCHONDRIAL DNA DEPLETION SYNDROME 8B (MNGIE TYPE)
+BMGC_DS13827,BMG_DS053593,"AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE"
+BMGC_DS13828,BMG_DS053594,RETINITIS PIGMENTOSA 53
+BMGC_DS13829,BMG_DS053595,CHROMOSOME 6q24-q25 DELETION SYNDROME
+BMGC_DS13830,BMG_DS053596,COMPLEMENT COMPONENT C1r/C1s DEFICIENCY
+BMGC_DS13831,BMG_DS053597,COMPLEMENT COMPONENT 2 DEFICIENCY
+BMGC_DS13832,BMG_DS053598,"AICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT"
+BMGC_DS13833,BMG_DS053599,"HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY"
+BMGC_DS13834,BMG_DS053600,"HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED"
+BMGC_DS13835,BMG_DS053602,"IMMUNODEFICIENCY, COMMON VARIABLE, 2"
+BMGC_DS13836,BMG_DS053604,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2"
+BMGC_DS13837,BMG_DS053605,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 3"
+BMGC_DS13838,BMG_DS053606,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5"
+BMGC_DS13839,BMG_DS053607,"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"
+BMGC_DS13841,BMG_DS053609,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3"
+BMGC_DS13842,BMG_DS053610,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2"
+BMGC_DS13843,BMG_DS053611,NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1
+BMGC_DS13844,BMG_DS053614,"EPILEPSY, HOT WATER, 2"
+BMGC_DS13845,BMG_DS053616,"pancreatic cancer, susceptibility to, 2"
+BMGC_DS13846,BMG_DS053617,"pancreatic cancer, susceptibility to, 3"
+BMGC_DS13847,BMG_DS053618,"MONONEUROPATHY OF THE MEDIAN NERVE, MILD"
+BMGC_DS13848,BMG_DS053619,CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME
+BMGC_DS13849,BMG_DS053620,"Maturity-onset diabetes of the young, type 10"
+BMGC_DS13850,BMG_DS053621,"Maturity-onset diabetes of the young, type 11"
+BMGC_DS13851,BMG_DS053622,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 4"
+BMGC_DS13852,BMG_DS053623,"BRACHYDACTYLY, TYPE E2"
+BMGC_DS13853,BMG_DS053624,"AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM"
+BMGC_DS13854,BMG_DS053625,"fatty liver disease, nonalcoholic, susceptibility to, 2"
+BMGC_DS13855,BMG_DS053626,FANCONI RENOTUBULAR SYNDROME 2
+BMGC_DS13856,BMG_DS053627,"FANCONI ANEMIA, COMPLEMENTATION GROUP O"
+BMGC_DS13857,BMG_DS053628,"DEAFNESS, AUTOSOMAL RECESSIVE 84A"
+BMGC_DS13858,BMG_DS053629,BIRBECK GRANULE DEFICIENCY
+BMGC_DS13859,BMG_DS053630,WARSAW BREAKAGE SYNDROME
+BMGC_DS13860,BMG_DS053631,"breast-ovarian cancer, familial, susceptibility to, 3"
+BMGC_DS13861,BMG_DS053634,"MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY"
+BMGC_DS13862,BMG_DS053635,"ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2"
+BMGC_DS13863,BMG_DS053636,CHROMOSOME 15q24 DELETION SYNDROME
+BMGC_DS13864,BMG_DS053637,CHROMOSOME 15q24 DUPLICATION SYNDROME
+BMGC_DS13865,BMG_DS053639,"autism, susceptibility to, 16"
+BMGC_DS13866,BMG_DS053640,OGUCHI DISEASE 2
+BMGC_DS13867,BMG_DS053641,"ESOPHAGITIS, EOSINOPHILIC, 2"
+BMGC_DS13868,BMG_DS053642,"CARDIOMYOPATHY, DILATED, 1R"
+BMGC_DS13869,BMG_DS053643,LEFT VENTRICULAR NONCOMPACTION 4
+BMGC_DS13870,BMG_DS053644,LEFT VENTRICULAR NONCOMPACTION 5
+BMGC_DS13871,BMG_DS053645,RETINITIS PIGMENTOSA 54
+BMGC_DS13872,BMG_DS053646,AMYOTROPHIC LATERAL SCLEROSIS 12
+BMGC_DS13873,BMG_DS053647,"autism, susceptibility to, 17"
+BMGC_DS13874,BMG_DS053648,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE"
+BMGC_DS13875,BMG_DS053649,"CHROMOSOME 16p11.2 DELETION SYNDROME, 220-KB"
+BMGC_DS13876,BMG_DS053650,FRONTONASAL DYSPLASIA 2
+BMGC_DS13877,BMG_DS053651,"DEAFNESS, AUTOSOMAL RECESSIVE 91"
+BMGC_DS13878,BMG_DS053652,FOXG1 syndrome
+BMGC_DS13879,BMG_DS053653,FRONTONASAL DYSPLASIA 3
+BMGC_DS13880,BMG_DS053654,CHROMOSOME 14q11-q22 DELETION SYNDROME
+BMGC_DS13881,BMG_DS053655,CHROMOSOME 16p13.3 DUPLICATION SYNDROME
+BMGC_DS13882,BMG_DS053656,RETINITIS PIGMENTOSA 51
+BMGC_DS13883,BMG_DS053657,"HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY"
+BMGC_DS13884,BMG_DS053658,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 5
+BMGC_DS13885,BMG_DS053659,LONG QT SYNDROME 13
+BMGC_DS13886,BMG_DS053660,Antibody Deficiency due to Defect in CD19
+BMGC_DS13887,BMG_DS053661,"IMMUNODEFICIENCY, COMMON VARIABLE, 4"
+BMGC_DS13888,BMG_DS053662,"IMMUNODEFICIENCY, COMMON VARIABLE, 5"
+BMGC_DS13889,BMG_DS053663,"IMMUNODEFICIENCY, COMMON VARIABLE, 6"
+BMGC_DS13890,BMG_DS053664,"AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE"
+BMGC_DS13891,BMG_DS053665,"AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE"
+BMGC_DS13892,BMG_DS053666,"AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE"
+BMGC_DS13893,BMG_DS053667,"AGAMMAGLOBULINEMIA 5, AUTOSOMAL DOMINANT"
+BMGC_DS13894,BMG_DS053668,GLYCOGEN STORAGE DISEASE XV
+BMGC_DS13895,BMG_DS053669,CHROMOSOME 4q21 DELETION SYNDROME
+BMGC_DS13896,BMG_DS053670,"MICROPHTHALMIA, ISOLATED 6"
+BMGC_DS13897,BMG_DS053672,"DERMATITIS, ATOPIC, 8"
+BMGC_DS13898,BMG_DS053673,"DERMATITIS, ATOPIC, 9"
+BMGC_DS13899,BMG_DS053674,myeloid neoplasm associated with FGFR1 rearrangement
+BMGC_DS13900,BMG_DS053675,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H"
+BMGC_DS13901,BMG_DS053676,CHROMOSOME 6q11-q14 DELETION SYNDROME
+BMGC_DS13902,BMG_DS053677,CHROMOSOME 6q13-q14 DELETION SYNDROME
+BMGC_DS13903,BMG_DS053679,NEPHRONOPHTHISIS 11
+BMGC_DS13904,BMG_DS053680,"autoimmune disease, susceptibility to, 6"
+BMGC_DS13905,BMG_DS053681,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7
+BMGC_DS13906,BMG_DS053682,"MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2"
+BMGC_DS13907,BMG_DS053683,CBL-related disorder
+BMGC_DS13908,BMG_DS053684,CHROMOSOME 2p12-p11.2 DELETION SYNDROME
+BMGC_DS13909,BMG_DS053685,ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1
+BMGC_DS13910,BMG_DS053686,RETINITIS PIGMENTOSA 55
+BMGC_DS13911,BMG_DS053687,ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2
+BMGC_DS13912,BMG_DS053688,RETINITIS PIGMENTOSA 56
+BMGC_DS13913,BMG_DS053689,RETINITIS PIGMENTOSA 57
+BMGC_DS13914,BMG_DS053690,OCCULT MACULAR DYSTROPHY
+BMGC_DS13915,BMG_DS053692,early repolarization associated with ventricular fibrillation
+BMGC_DS13916,BMG_DS053693,CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME
+BMGC_DS13917,BMG_DS053694,"CHROMOSOME 16p12.2-p11.2 DELETION SYNDROME, 7.1- TO 8.7-MB"
+BMGC_DS13918,BMG_DS053695,FORSYTHE-WAKELING SYNDROME
+BMGC_DS13919,BMG_DS053696,"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3"
+BMGC_DS13920,BMG_DS053697,CRANIOECTODERMAL DYSPLASIA 2
+BMGC_DS13921,BMG_DS053698,"Lymphedema, posterior choanal atresia syndrome"
+BMGC_DS13922,BMG_DS053699,COG5 congenital disorder of glycosylation
+BMGC_DS13923,BMG_DS053700,SENIOR-LOKEN SYNDROME 7
+BMGC_DS13924,BMG_DS053701,Primary hyperoxaluria type III
+BMGC_DS13925,BMG_DS053702,RETINITIS PIGMENTOSA 58
+BMGC_DS13926,BMG_DS053703,CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME
+BMGC_DS13927,BMG_DS053705,"FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2"
+BMGC_DS13928,BMG_DS053707,Fetal encasement syndrome
+BMGC_DS13929,BMG_DS053709,19p13.13 microdeletion syndrome
+BMGC_DS13930,BMG_DS053710,CHROMOSOME 19p13.13 DUPLICATION SYNDROME
+BMGC_DS13931,BMG_DS053711,Hereditary sensory autonomic neuropathy type IC
+BMGC_DS13932,BMG_DS053712,"CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B"
+BMGC_DS13933,BMG_DS053713,"CARDIOMYOPATHY, DILATED, 1GG"
+BMGC_DS13934,BMG_DS053714,"Parkinson disease 5, autosomal dominant, susceptibility to"
+BMGC_DS13935,BMG_DS053715,"SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE"
+BMGC_DS13936,BMG_DS053716,C1q DEFICIENCY 1
+BMGC_DS13937,BMG_DS053717,D-2-HYDROXYGLUTARIC ACIDURIA 2
+BMGC_DS13938,BMG_DS053718,Brain calcification Rajab type
+BMGC_DS13939,BMG_DS053719,CONE-ROD DYSTROPHY 15
+BMGC_DS13940,BMG_DS053720,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip"
+BMGC_DS13941,BMG_DS053721,MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE)
+BMGC_DS13942,BMG_DS053722,"MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY"
+BMGC_DS13943,BMG_DS053723,"Anterior maxillary protrusion, strabismus, intellectual disability syndrome"
+BMGC_DS13944,BMG_DS053724,"SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE"
+BMGC_DS13945,BMG_DS053725,Congenital dyserythropoietic anemia type IV
+BMGC_DS13946,BMG_DS053726,VESICOURETERAL REFLUX 3
+BMGC_DS13947,BMG_DS053727,THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome
+BMGC_DS13948,BMG_DS053728,CHROMOSOME 2q31.1 DUPLICATION SYNDROME
+BMGC_DS13949,BMG_DS053729,RUBINSTEIN-TAYBI SYNDROME 2
+BMGC_DS13950,BMG_DS053730,"SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE"
+BMGC_DS13951,BMG_DS053731,Long Qt Syndrome 2
+BMGC_DS13952,BMG_DS053732,MAMMARY-DIGITAL-NAIL SYNDROME
+BMGC_DS13953,BMG_DS053733,Long Qt Syndrome 6
+BMGC_DS13954,BMG_DS053734,"Cardiomyopathy, Dilated, 1V"
+BMGC_DS13955,BMG_DS053735,"KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT"
+BMGC_DS13956,BMG_DS053736,"microphthalmia, isolated, with coloboma 6"
+BMGC_DS13957,BMG_DS053737,"MICROPHTHALMIA, ISOLATED 7"
+BMGC_DS13958,BMG_DS053738,NOONAN SYNDROME 7
+BMGC_DS13959,BMG_DS053739,LEOPARD SYNDROME 3
+BMGC_DS13960,BMG_DS053740,"NEUROPATHY, HEREDITARY SENSORY, TYPE ID"
+BMGC_DS13961,BMG_DS053741,Progressive polyneuropathy with bilateral striatal necrosis
+BMGC_DS13962,BMG_DS053742,"Hirschsprung disease, susceptibility to, 3"
+BMGC_DS13963,BMG_DS053743,"Hirschsprung disease, susceptibility to, 4"
+BMGC_DS13964,BMG_DS053744,TREACHER COLLINS SYNDROME 2
+BMGC_DS13965,BMG_DS053745,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7"
+BMGC_DS13966,BMG_DS053746,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11"
+BMGC_DS13967,BMG_DS053747,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 12
+BMGC_DS13968,BMG_DS053748,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q"
+BMGC_DS13969,BMG_DS053749,Deficiency of sterol carrier protein X
+BMGC_DS13970,BMG_DS053750,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10"
+BMGC_DS13971,BMG_DS053752,"HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS"
+BMGC_DS13972,BMG_DS053753,Retinitis Pigmentosa 4
+BMGC_DS13973,BMG_DS053754,"ACNE INVERSA, FAMILIAL, 2, WITH OR WITHOUT DOWLING-DEGOS DISEASE"
+BMGC_DS13974,BMG_DS053755,"ACNE INVERSA, FAMILIAL, 3"
+BMGC_DS13975,BMG_DS053756,"Cardiomyopathy, Dilated, 1t"
+BMGC_DS13976,BMG_DS053757,"ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE"
+BMGC_DS13977,BMG_DS053758,"SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE"
+BMGC_DS13978,BMG_DS053759,"HETEROTAXY, VISCERAL, 4, AUTOSOMAL"
+BMGC_DS13979,BMG_DS053760,S-adenosylhomocysteine hydrolase deficiency
+BMGC_DS13980,BMG_DS053761,RETINITIS PIGMENTOSA 49
+BMGC_DS13981,BMG_DS053762,"Macular Degeneration, Age-Related, 6"
+BMGC_DS13982,BMG_DS053763,RETINITIS PIGMENTOSA 47
+BMGC_DS13983,BMG_DS053764,"IMMUNODEFICIENCY 90 WITH ENCEPHALOPATHY, FUNCTIONAL HYPOSPLENIA, AND HEPATIC DYSFUNCTION"
+BMGC_DS13984,BMG_DS053765,"MACULAR DEGENERATION, AGE-RELATED, 5"
+BMGC_DS13985,BMG_DS053766,"46,XY SEX REVERSAL 6"
+BMGC_DS13986,BMG_DS053768,RETINITIS PIGMENTOSA 45
+BMGC_DS13987,BMG_DS053769,RETINITIS PIGMENTOSA 44
+BMGC_DS13988,BMG_DS053770,CHROMOSOME 17p13.1 DELETION SYNDROME
+BMGC_DS13989,BMG_DS053771,"MACULAR DEGENERATION, AGE-RELATED, 8"
+BMGC_DS13990,BMG_DS053772,"COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE"
+BMGC_DS13991,BMG_DS053773,"AORTIC ANEURYSM, FAMILIAL THORACIC 7"
+BMGC_DS13992,BMG_DS053774,Complement Component C1s Deficiency
+BMGC_DS13993,BMG_DS053775,"MACULAR DEGENERATION, AGE-RELATED, 12"
+BMGC_DS13994,BMG_DS053776,"COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II"
+BMGC_DS13995,BMG_DS053777,"COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I"
+BMGC_DS13996,BMG_DS053778,MASP2 Deficiency
+BMGC_DS13997,BMG_DS053779,Retinitis Pigmentosa 20
+BMGC_DS13998,BMG_DS053780,LOEYS-DIETZ SYNDROME 3
+BMGC_DS13999,BMG_DS053781,IMMUNODEFICIENCY 31B
+BMGC_DS14000,BMG_DS053782,MEIER-GORLIN SYNDROME 2
+BMGC_DS14001,BMG_DS053783,RETINITIS PIGMENTOSA 40
+BMGC_DS14002,BMG_DS053784,MEIER-GORLIN SYNDROME 3
+BMGC_DS14003,BMG_DS053785,MEIER-GORLIN SYNDROME 4
+BMGC_DS14004,BMG_DS053786,MEIER-GORLIN SYNDROME 5
+BMGC_DS14005,BMG_DS053787,"CILIARY DYSKINESIA, PRIMARY, 14"
+BMGC_DS14006,BMG_DS053788,"CILIARY DYSKINESIA, PRIMARY, 15"
+BMGC_DS14007,BMG_DS053789,RETINITIS PIGMENTOSA 39
+BMGC_DS14008,BMG_DS053790,RETINITIS PIGMENTOSA 43
+BMGC_DS14009,BMG_DS053791,"PONTOCEREBELLAR HYPOPLASIA, TYPE 2D"
+BMGC_DS14010,BMG_DS053793,"Bile Acid Synthesis Defect, Congenital, 3"
+BMGC_DS14011,BMG_DS053794,SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY
+BMGC_DS14012,BMG_DS053795,NEPHRONOPHTHISIS 12
+BMGC_DS14013,BMG_DS053796,SECKEL SYNDROME 5
+BMGC_DS14014,BMG_DS053797,NEPHRONOPHTHISIS 9
+BMGC_DS14015,BMG_DS053798,C9 Deficiency
+BMGC_DS14016,BMG_DS053799,RETINITIS PIGMENTOSA 48
+BMGC_DS14017,BMG_DS053800,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 8"
+BMGC_DS14018,BMG_DS053801,LEBER CONGENITAL AMAUROSIS 7
+BMGC_DS14019,BMG_DS053802,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D"
+BMGC_DS14020,BMG_DS053803,Multisystemic smooth muscle dysfunction syndrome
+BMGC_DS14021,BMG_DS053804,LEBER CONGENITAL AMAUROSIS 8
+BMGC_DS14022,BMG_DS053805,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16"
+BMGC_DS14023,BMG_DS053806,Megaloblastic Anemia due to Dihydrofolate Reductase Deficiency
+BMGC_DS14024,BMG_DS053807,LEBER CONGENITAL AMAUROSIS 15
+BMGC_DS14025,BMG_DS053808,"Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome"
+BMGC_DS14026,BMG_DS053809,"OSTEOGENESIS IMPERFECTA, TYPE X"
+BMGC_DS14027,BMG_DS053810,"OSTEOGENESIS IMPERFECTA, TYPE XI"
+BMGC_DS14028,BMG_DS053811,FUCOSYLTRANSFERASE 6 DEFICIENCY
+BMGC_DS14029,BMG_DS053812,"congenital heart defects, multiple types, 6"
+BMGC_DS14030,BMG_DS053813,OROFACIAL CLEFT 13
+BMGC_DS14031,BMG_DS053814,FICOLIN 3 DEFICIENCY
+BMGC_DS14032,BMG_DS053815,RETINITIS PIGMENTOSA 59
+BMGC_DS14033,BMG_DS053816,RETINITIS PIGMENTOSA 38
+BMGC_DS14034,BMG_DS053817,"FEBRILE SEIZURES, FAMILIAL, 3B"
+BMGC_DS14035,BMG_DS053818,"DEAFNESS, AUTOSOMAL RECESSIVE 61"
+BMGC_DS14036,BMG_DS053819,"Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction"
+BMGC_DS14037,BMG_DS053820,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17"
+BMGC_DS14038,BMG_DS053821,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18"
+BMGC_DS14039,BMG_DS053822,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20"
+BMGC_DS14040,BMG_DS053823,"CARDIOMYOPATHY, DILATED, 1HH"
+BMGC_DS14041,BMG_DS053824,"HYPOMAGNESEMIA 6, RENAL"
+BMGC_DS14042,BMG_DS053825,chromosome 13q14 deletion syndrome
+BMGC_DS14043,BMG_DS053826,"Obesity, Hyperphagia, and Developmental Delay"
+BMGC_DS14044,BMG_DS053827,CATARACT 36
+BMGC_DS14045,BMG_DS053828,SPINOCEREBELLAR ATAXIA 32
+BMGC_DS14046,BMG_DS053829,"LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3, WITH OR WITHOUT GLOMERULONEPHRITIS"
+BMGC_DS14047,BMG_DS053830,"DEAFNESS, AUTOSOMAL RECESSIVE 89"
+BMGC_DS14048,BMG_DS053831,MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A
+BMGC_DS14049,BMG_DS053832,"MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT"
+BMGC_DS14050,BMG_DS053833,ALOPECIA-INTELLECTUAL DISABILITY SYNDROME 3
+BMGC_DS14051,BMG_DS053834,"PARASOMNIA, SLEEPWALKING TYPE"
+BMGC_DS14052,BMG_DS053835,"PARASOMNIA, SLEEP TERRORS TYPE"
+BMGC_DS14053,BMG_DS053836,"IgA nephropathy, susceptibility to, 2"
+BMGC_DS14054,BMG_DS053837,OKT4 EPITOPE DEFICIENCY
+BMGC_DS14055,BMG_DS053838,schizophrenia 15
+BMGC_DS14056,BMG_DS053839,"AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 2"
+BMGC_DS14057,BMG_DS053840,"CANDIDIASIS, FAMILIAL, 6"
+BMGC_DS14058,BMG_DS053841,SPERMATOGENIC FAILURE 8
+BMGC_DS14059,BMG_DS053842,SPERMATOGENIC FAILURE 9
+BMGC_DS14060,BMG_DS053843,SCHIZOPHRENIA 16
+BMGC_DS14061,BMG_DS053844,"GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 3"
+BMGC_DS14062,BMG_DS053845,"MYOPIA 19, AUTOSOMAL DOMINANT"
+BMGC_DS14063,BMG_DS053846,"intellectual disability, autosomal dominant 6"
+BMGC_DS14064,BMG_DS053847,"melanoma, cutaneous malignant, susceptibility to, 6"
+BMGC_DS14065,BMG_DS053848,"CYANOSIS, TRANSIENT NEONATAL"
+BMGC_DS14066,BMG_DS053849,"ATRIAL FIBRILLATION, FAMILIAL, 9"
+BMGC_DS14067,BMG_DS053850,HYPOTRICHOSIS 3
+BMGC_DS14068,BMG_DS053851,"OSTEOGENESIS IMPERFECTA, TYPE XII"
+BMGC_DS14069,BMG_DS053852,RETINITIS PIGMENTOSA 60
+BMGC_DS14070,BMG_DS053853,"PITUITARY HORMONE DEFICIENCY, COMBINED, 6"
+BMGC_DS14071,BMG_DS053854,"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 2"
+BMGC_DS14072,BMG_DS053855,"dyskeratosis congenita, autosomal recessive 3"
+BMGC_DS14073,BMG_DS053856,"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2"
+BMGC_DS14074,BMG_DS053857,autosomal recessive dyskeratosis congenita 4
+BMGC_DS14075,BMG_DS053858,"dyskeratosis congenita, autosomal dominant 3"
+BMGC_DS14076,BMG_DS053859,Nestor Guillermo progeria syndrome
+BMGC_DS14077,BMG_DS053860,"CILIARY DYSKINESIA, PRIMARY, 16"
+BMGC_DS14078,BMG_DS053861,LISSENCEPHALY 4 WITH MICROCEPHALY
+BMGC_DS14079,BMG_DS053862,"intellectual disability, autosomal recessive 14"
+BMGC_DS14080,BMG_DS053863,"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3"
+BMGC_DS14081,BMG_DS053864,"ATRIAL FIBRILLATION, FAMILIAL, 10"
+BMGC_DS14082,BMG_DS053865,PROTEIN Z DEFICIENCY
+BMGC_DS14083,BMG_DS053866,hyperlipidemia due to hepatic triglyceride lipase deficiency
+BMGC_DS14084,BMG_DS053867,Apolipoprotein C-III Deficiency
+BMGC_DS14085,BMG_DS053868,MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA)
+BMGC_DS14086,BMG_DS053869,"HYPERCALCIURIA, CHILDHOOD, SELF-LIMITING"
+BMGC_DS14087,BMG_DS053870,"CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA"
+BMGC_DS14088,BMG_DS053872,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3"
+BMGC_DS14089,BMG_DS053873,CONGENITAL MYOPATHY 11
+BMGC_DS14090,BMG_DS053874,"NEPHROTIC SYNDROME, TYPE 4"
+BMGC_DS14091,BMG_DS053875,"NYSTAGMUS 8, CONGENITAL, AUTOSOMAL RECESSIVE"
+BMGC_DS14092,BMG_DS053876,"BLOUNT DISEASE, ADOLESCENT"
+BMGC_DS14093,BMG_DS053877,"ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OF PHALANGES AND METACARPALS/METATARSALS"
+BMGC_DS14094,BMG_DS053878,"ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY"
+BMGC_DS14095,BMG_DS053879,ANTERIOR SEGMENT DYSGENESIS 7
+BMGC_DS14096,BMG_DS053880,"ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND IMPAIRED INTELLECTUAL DEVELOPMENT"
+BMGC_DS14097,BMG_DS053882,"NYSTAGMUS 6, CONGENITAL, X-LINKED"
+BMGC_DS14098,BMG_DS053883,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6
+BMGC_DS14099,BMG_DS053884,CK syndrome
+BMGC_DS14100,BMG_DS053885,"46,XX SEX REVERSAL 3"
+BMGC_DS14101,BMG_DS053886,CHROMOSOME Xq26 DELETION SYNDROME
+BMGC_DS14102,BMG_DS053887,"MACULAR DEGENERATION, ATROPHIC, X-LINKED"
+BMGC_DS14103,BMG_DS053889,"MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM, AND FACIAL DYSMORPHISM"
+BMGC_DS14104,BMG_DS053890,"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED"
+BMGC_DS14105,BMG_DS053892,"DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL"
+BMGC_DS14106,BMG_DS053893,"MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT"
+BMGC_DS14107,BMG_DS053895,"RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA"
+BMGC_DS14108,BMG_DS053898,D-2-HYDROXYGLUTARIC ACIDURIA 1
+BMGC_DS14109,BMG_DS053899,"EPIPHYSEAL DYSPLASIA, MULTIPLE, 3, WITH MYOPATHY"
+BMGC_DS14110,BMG_DS053900,"USH1D/F, CDH23/PCDH15, DIGENIC"
+BMGC_DS14111,BMG_DS053901,LEFT VENTRICULAR NONCOMPACTION 3
+BMGC_DS14112,BMG_DS053902,"AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE"
+BMGC_DS14113,BMG_DS053904,"melanoma, cutaneous malignant, susceptibility to, 8"
+BMGC_DS14114,BMG_DS053906,BORNHOLM EYE DISEASE
+BMGC_DS14115,BMG_DS053907,"SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE"
+BMGC_DS14116,BMG_DS053908,"PARKINSON DISEASE, LATE-ONSET"
+BMGC_DS14117,BMG_DS053909,"IgA nephropathy, susceptibility to, 1"
+BMGC_DS14118,BMG_DS053910,"Cardiomyopathy, Dilated, 1u"
+BMGC_DS14119,BMG_DS053911,thrombophilia due to thrombin defect
+BMGC_DS14120,BMG_DS053912,"DEAFNESS, AUTOSOMAL DOMINANT 51"
+BMGC_DS14121,BMG_DS053913,"FANCONI ANEMIA, COMPLEMENTATION GROUP D2"
+BMGC_DS14122,BMG_DS053914,"FANCONI ANEMIA, COMPLEMENTATION GROUP E"
+BMGC_DS14123,BMG_DS053915,"DEAFNESS, AUTOSOMAL RECESSIVE 85"
+BMGC_DS14124,BMG_DS053919,Posterior reversible encephalopathy syndrome
+BMGC_DS14125,BMG_DS053931,Secondary spontaneous pneumothorax
+BMGC_DS14126,BMG_DS053938,hemoglobin H disease
+BMGC_DS14127,BMG_DS053939,Hydrops fetalis due to alpha thalassemia
+BMGC_DS14128,BMG_DS053956,Primary immunoglobulin A nephropathy (disorder)
+BMGC_DS14129,BMG_DS053976,Recurrent lower respiratory tract infection
+BMGC_DS14130,BMG_DS053983,Sepsis caused by Gram negative bacteria
+BMGC_DS14131,BMG_DS054033,Adult onset autosomal dominant leukodystrophy
+BMGC_DS14132,BMG_DS054035,Sepsis caused by methicillin resistant Staphylococcus aureus
+BMGC_DS14133,BMG_DS054147,Widespread Chronic Pain
+BMGC_DS14134,BMG_DS054149,Heterotaxy Syndrome
+BMGC_DS14135,BMG_DS054150,right atrial isomerism
+BMGC_DS14136,BMG_DS054155,Bilateral Slipped Capital Femoral Epiphyses
+BMGC_DS14137,BMG_DS054156,Unilateral Slipped Capital Femoral Epiphyses
+BMGC_DS14138,BMG_DS054167,Disseminated Fusariosis
+BMGC_DS14139,BMG_DS054168,Pulmonary Fusariosis
+BMGC_DS14140,BMG_DS054173,GALNS Deficiency
+BMGC_DS14141,BMG_DS054174,Osteopetrosis Autosomal Dominant Type 2
+BMGC_DS14142,BMG_DS054175,Pott's Paraplegia
+BMGC_DS14143,BMG_DS054176,"Niemann-Pick Disease, Type C1"
+BMGC_DS14144,BMG_DS054180,Linear Verrucous Epidermal Nevus
+BMGC_DS14145,BMG_DS054182,Microdeletion 15q11.2
+BMGC_DS14146,BMG_DS054183,Non-Infective Endocarditis
+BMGC_DS14147,BMG_DS054185,Hyperheparinemia
+BMGC_DS14148,BMG_DS054186,Factor II deficiency
+BMGC_DS14149,BMG_DS054189,Axial Spondyloarthritis
+BMGC_DS14150,BMG_DS054192,Precordial Catch Syndrome
+BMGC_DS14151,BMG_DS054194,Nonalcoholic Steatohepatitis
+BMGC_DS14152,BMG_DS054201,Miliaria crystallina
+BMGC_DS14153,BMG_DS054205,Familial renal glucosuria
+BMGC_DS14154,BMG_DS054214,MYOTONIC DYSTROPHY 1
+BMGC_DS14155,BMG_DS054515,Lupoid hepatitis NEC
+BMGC_DS14156,BMG_DS054557,Mixed Astigmatism
+BMGC_DS14157,BMG_DS054558,Oblique Astigmatism
+BMGC_DS14158,BMG_DS054568,orofacial cleft
+BMGC_DS14159,BMG_DS054592,Multiple Chronic Conditions
+BMGC_DS14160,BMG_DS054609,2-methyl-3-hydroxybutyric aciduria
+BMGC_DS14161,BMG_DS054616,"Atypical Mycobacteriosis, Familial"
+BMGC_DS14162,BMG_DS054618,Waardenburg Syndrome
+BMGC_DS14163,BMG_DS054641,colon serrated polyposis
+BMGC_DS14164,BMG_DS054643,gastrointestinal hamartoma
+BMGC_DS14165,BMG_DS054649,familial adenomatous polyposis 2
+BMGC_DS14166,BMG_DS054656,appendix L-cell glucagon-like peptide-producing neuroendocrine tumor
+BMGC_DS14167,BMG_DS054657,colonic L-cell glucagon-like peptide producing tumor
+BMGC_DS14168,BMG_DS054658,L-cell glucagon-like peptide-producing neuroendocrine tumor
+BMGC_DS14169,BMG_DS054659,small intestinal L-cell glucagon-like peptide producing tumor
+BMGC_DS14170,BMG_DS054663,"MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS"
+BMGC_DS14171,BMG_DS054664,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, RAYMOND TYPE"
+BMGC_DS14172,BMG_DS054665,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 96"
+BMGC_DS14173,BMG_DS054666,"autism, susceptibility to, X-linked 5"
+BMGC_DS14174,BMG_DS054667,"intellectual disability, X-linked 90"
+BMGC_DS14175,BMG_DS054668,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 88"
+BMGC_DS14176,BMG_DS054669,"X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia"
+BMGC_DS14177,BMG_DS054670,"renal cell carcinoma, Xp11-associated"
+BMGC_DS14178,BMG_DS054671,Ogden syndrome
+BMGC_DS14179,BMG_DS054673,AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA
+BMGC_DS14180,BMG_DS054674,syndromic X-linked intellectual disability 17
+BMGC_DS14181,BMG_DS054675,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE"
+BMGC_DS14182,BMG_DS054676,syndromic X-linked intellectual disability Chudley-Schwartz type
+BMGC_DS14183,BMG_DS054677,"CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA"
+BMGC_DS14184,BMG_DS054678,"X-linked cerebral, cerebellar, coloboma syndrome"
+BMGC_DS14185,BMG_DS054679,KABUKI SYNDROME 2
+BMGC_DS14186,BMG_DS054680,MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2
+BMGC_DS14187,BMG_DS054681,CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME
+BMGC_DS14188,BMG_DS054682,"NAIL DISORDER, NONSYNDROMIC CONGENITAL, 6"
+BMGC_DS14189,BMG_DS054683,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 16"
+BMGC_DS14190,BMG_DS054684,"omphalocele, X-linked"
+BMGC_DS14191,BMG_DS054686,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1"
+BMGC_DS14192,BMG_DS054688,"renal dysplasia, cystic, susceptibility to"
+BMGC_DS14193,BMG_DS054690,"LUNG AGENESIS, CONGENITAL HEART DEFECTS, AND THUMB ANOMALIES SYNDROME"
+BMGC_DS14194,BMG_DS054691,"leukemia, acute myeloid, susceptibility to"
+BMGC_DS14195,BMG_DS054693,THROMBOCYTHEMIA 2
+BMGC_DS14196,BMG_DS054695,ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS
+BMGC_DS14197,BMG_DS054696,"ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2"
+BMGC_DS14198,BMG_DS054697,ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE
+BMGC_DS14199,BMG_DS054698,"LONG QT SYNDROME 2/3, DIGENIC"
+BMGC_DS14200,BMG_DS054699,"LONG QT SYNDROME 3/6, DIGENIC"
+BMGC_DS14201,BMG_DS054700,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1"
+BMGC_DS14202,BMG_DS054702,Multiple mitochondrial dysfunctions syndrome type 1
+BMGC_DS14203,BMG_DS054703,"CUTIS LAXA, AUTOSOMAL DOMINANT 1"
+BMGC_DS14204,BMG_DS054704,"OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY"
+BMGC_DS14205,BMG_DS054707,Small Fiber Neuropathy
+BMGC_DS14206,BMG_DS054713,KOILONYCHIA WITH LEUKONYCHIA
+BMGC_DS14207,BMG_DS054714,"BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT"
+BMGC_DS14208,BMG_DS054715,CHROMOSOME 2q23.1 DELETION SYNDROME
+BMGC_DS14209,BMG_DS054717,"OMPHALOCELE, AUTOSOMAL"
+BMGC_DS14210,BMG_DS054719,THROMBOCYTHEMIA 1
+BMGC_DS14211,BMG_DS054721,"LONG QT SYNDROME 1/2, DIGENIC"
+BMGC_DS14212,BMG_DS054722,vitiligo-associated multiple autoimmune disease susceptibility 6
+BMGC_DS14213,BMG_DS054723,JOUBERT SYNDROME 12
+BMGC_DS14214,BMG_DS054724,"17,20-Lyase Deficiency, Isolated"
+BMGC_DS14215,BMG_DS054725,"NAIL DISORDER, NONSYNDROMIC CONGENITAL, 4"
+BMGC_DS14216,BMG_DS054727,FIBROCHONDROGENESIS 1
+BMGC_DS14217,BMG_DS054728,"GALACTOSEMIA, DUARTE VARIANT"
+BMGC_DS14218,BMG_DS054729,GELEOPHYSIC DYSPLASIA 1
+BMGC_DS14219,BMG_DS054730,"BERNARD-SOULIER SYNDROME, TYPE A1"
+BMGC_DS14220,BMG_DS054731,"GLAUCOMA, PRIMARY OPEN ANGLE, ADULT-ONSET"
+BMGC_DS14221,BMG_DS054732,"GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET"
+BMGC_DS14222,BMG_DS054733,GLUTARIC ACIDEMIA IIA
+BMGC_DS14223,BMG_DS054734,GLUTARIC ACIDEMIA IIB
+BMGC_DS14224,BMG_DS054735,GLUTARIC ACIDEMIA IIC
+BMGC_DS14225,BMG_DS054738,"THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT"
+BMGC_DS14226,BMG_DS054742,"ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS, FAMILIAL"
+BMGC_DS14227,BMG_DS054745,HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY
+BMGC_DS14228,BMG_DS054746,"MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS"
+BMGC_DS14229,BMG_DS054747,"MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1"
+BMGC_DS14230,BMG_DS054749,OROTIC ACIDURIA WITHOUT MEGALOBLASTIC ANEMIA
+BMGC_DS14231,BMG_DS054750,"LIVER FAILURE, INFANTILE, TRANSIENT"
+BMGC_DS14232,BMG_DS054756,"LONG QT SYNDROME 2/5, DIGENIC"
+BMGC_DS14233,BMG_DS054757,JOUBERT SYNDROME 11
+BMGC_DS14234,BMG_DS054763,HYPOTRICHOSIS 8
+BMGC_DS14235,BMG_DS054764,Cryptozoospermia
+BMGC_DS14236,BMG_DS054766,"HEMOGLOBIN H DISEASE, NONDELETIONAL"
+BMGC_DS14237,BMG_DS054767,"Osteogenesis Imperfecta, Type VI"
+BMGC_DS14238,BMG_DS054768,"bleeding disorder, platelet-type, 13, susceptibility to"
+BMGC_DS14239,BMG_DS054770,Glyoxalase II Deficiency
+BMGC_DS14240,BMG_DS054771,"DEAFNESS, AUTOSOMAL RECESSIVE 29"
+BMGC_DS14241,BMG_DS054773,Leukotriene C4 Synthase Deficiency
+BMGC_DS14242,BMG_DS054774,Emberger Syndrome
+BMGC_DS14243,BMG_DS054775,Perisylvian polymicrogyria
+BMGC_DS14244,BMG_DS054776,MOYAMOYA DISEASE 5
+BMGC_DS14245,BMG_DS054777,"ATRIAL FIBRILLATION, FAMILIAL, 11"
+BMGC_DS14246,BMG_DS054778,"ATRIAL FIBRILLATION, FAMILIAL, 12"
+BMGC_DS14247,BMG_DS054779,"Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency"
+BMGC_DS14248,BMG_DS054780,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3"
+BMGC_DS14249,BMG_DS054781,N-ACETYLASPARTATE DEFICIENCY
+BMGC_DS14250,BMG_DS054782,"MYOPATHY, DISTAL, 4"
+BMGC_DS14251,BMG_DS054783,"SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE"
+BMGC_DS14252,BMG_DS054784,"SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE"
+BMGC_DS14253,BMG_DS054785,IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2
+BMGC_DS14254,BMG_DS054786,"psoriasis 13, susceptibility to"
+BMGC_DS14255,BMG_DS054787,HERMANSKY-PUDLAK SYNDROME 7
+BMGC_DS14256,BMG_DS054788,Chondrodysplasia with joint dislocations gPAPP type
+BMGC_DS14257,BMG_DS054790,"aspergillosis, susceptibility to"
+BMGC_DS14258,BMG_DS054791,multiple congenital anomalies-hypotonia-seizures syndrome 1
+BMGC_DS14259,BMG_DS054792,ANHAPTOGLOBINEMIA
+BMGC_DS14260,BMG_DS054793,HYPOHAPTOGLOBINEMIA
+BMGC_DS14261,BMG_DS054794,Atrial Septal Defect 3
+BMGC_DS14262,BMG_DS054795,"sick sinus syndrome 3, susceptibility to"
+BMGC_DS14263,BMG_DS054796,SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
+BMGC_DS14264,BMG_DS054797,Keppen Lubinsky syndrome
+BMGC_DS14265,BMG_DS054798,CRANIOECTODERMAL DYSPLASIA 3
+BMGC_DS14266,BMG_DS054799,Kappa-Chain Deficiency
+BMGC_DS14267,BMG_DS054800,Methylmalonate Semialdehyde Dehydrogenase Deficiency
+BMGC_DS14268,BMG_DS054801,Pyruvate Dehydrogenase E1-Beta Deficiency
+BMGC_DS14269,BMG_DS054802,"intellectual disability, autosomal dominant 2"
+BMGC_DS14270,BMG_DS054803,mosaic variegated aneuploidy syndrome 2
+BMGC_DS14271,BMG_DS054804,"CORTICAL MALFORMATIONS, OCCIPITAL"
+BMGC_DS14272,BMG_DS054806,Hereditary Sensory and Autonomic Neuropathy Type Ie
+BMGC_DS14273,BMG_DS054807,hydrolethalus syndrome 2
+BMGC_DS14274,BMG_DS054808,CHITOTRIOSIDASE DEFICIENCY
+BMGC_DS14275,BMG_DS054809,Lactate Dehydrogenase B Deficiency
+BMGC_DS14276,BMG_DS054810,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6
+BMGC_DS14277,BMG_DS054811,"STICKLER SYNDROME, TYPE IV"
+BMGC_DS14278,BMG_DS054812,"NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9"
+BMGC_DS14279,BMG_DS054813,"DEAFNESS, AUTOSOMAL DOMINANT 64"
+BMGC_DS14280,BMG_DS054814,Hyperbiliverdinemia
+BMGC_DS14281,BMG_DS054815,"CANDIDIASIS, FAMILIAL, 7"
+BMGC_DS14282,BMG_DS054816,"delayed sleep phase syndrome, susceptibility to"
+BMGC_DS14283,BMG_DS054817,PARAGANGLIOMAS 5
+BMGC_DS14284,BMG_DS054819,"MYOPIA 21, AUTOSOMAL DOMINANT"
+BMGC_DS14285,BMG_DS054820,BRITTLE CORNEA SYNDROME 2
+BMGC_DS14286,BMG_DS054821,Developmental Dysplasia of the Hip
+BMGC_DS14287,BMG_DS054822,HERMANSKY-PUDLAK SYNDROME 9
+BMGC_DS14288,BMG_DS054823,GATA2 Deficiency
+BMGC_DS14289,BMG_DS054824,JOUBERT SYNDROME 13
+BMGC_DS14290,BMG_DS054825,"MECKEL SYNDROME, TYPE 10"
+BMGC_DS14291,BMG_DS054826,RETINITIS PIGMENTOSA 61
+BMGC_DS14292,BMG_DS054827,RETINITIS PIGMENTOSA 62
+BMGC_DS14293,BMG_DS054828,GELEOPHYSIC DYSPLASIA 2
+BMGC_DS14294,BMG_DS054829,LEBER CONGENITAL AMAUROSIS 16
+BMGC_DS14295,BMG_DS054830,CRANIOSYNOSTOSIS AND DENTAL ANOMALIES
+BMGC_DS14296,BMG_DS054831,"PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3"
+BMGC_DS14297,BMG_DS054832,CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME
+BMGC_DS14298,BMG_DS054833,"NEPHROTIC SYNDROME, TYPE 6"
+BMGC_DS14299,BMG_DS054834,"MYASTHENIC SYNDROME, CONGENITAL, 16"
+BMGC_DS14300,BMG_DS054835,"NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES"
+BMGC_DS14301,BMG_DS054836,Glycoprotein IA Deficiency
+BMGC_DS14302,BMG_DS054837,Glycoprotein VI deficiency
+BMGC_DS14303,BMG_DS054838,RAFIQ SYNDROME
+BMGC_DS14304,BMG_DS054839,PARKINSON DISEASE 17
+BMGC_DS14305,BMG_DS054840,THREE M SYNDROME 3
+BMGC_DS14306,BMG_DS054841,HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 3
+BMGC_DS14307,BMG_DS054842,"intellectual disability, autosomal recessive 16"
+BMGC_DS14308,BMG_DS054843,"MECKEL SYNDROME, TYPE 9"
+BMGC_DS14309,BMG_DS054845,"encephalopathy, acute, infection-induced, susceptibility to, 4"
+BMGC_DS14310,BMG_DS054846,"NEUROPATHY, HEREDITARY SENSORY, TYPE IIC"
+BMGC_DS14311,BMG_DS054847,ADAMS-OLIVER SYNDROME 2
+BMGC_DS14312,BMG_DS054848,"BILIARY CIRRHOSIS, PRIMARY, 4"
+BMGC_DS14313,BMG_DS054849,"BILIARY CIRRHOSIS, PRIMARY, 5"
+BMGC_DS14314,BMG_DS054850,WARBURG MICRO SYNDROME 3
+BMGC_DS14315,BMG_DS054852,RETINAL ARTERIAL MACROANEURYSM WITH SUPRAVALVULAR PULMONIC STENOSIS
+BMGC_DS14316,BMG_DS054854,WARBURG MICRO SYNDROME 2
+BMGC_DS14317,BMG_DS054855,HOLOPROSENCEPHALY 11
+BMGC_DS14318,BMG_DS054856,"HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3"
+BMGC_DS14319,BMG_DS054857,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O"
+BMGC_DS14320,BMG_DS054858,CHROMOSOME 8q21.11 DELETION SYNDROME
+BMGC_DS14321,BMG_DS054859,"MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME 1"
+BMGC_DS14322,BMG_DS054860,HYPOTRICHOSIS 9
+BMGC_DS14323,BMG_DS054861,HYPOTRICHOSIS 10
+BMGC_DS14324,BMG_DS054862,"intellectual disability, autosomal recessive 18"
+BMGC_DS14325,BMG_DS054863,NARCOLEPSY 7
+BMGC_DS14326,BMG_DS054864,"Parkinson disease 18, autosomal dominant, susceptibility to"
+BMGC_DS14327,BMG_DS054865,"ANEURYSM, INTRACRANIAL BERRY, 11"
+BMGC_DS14328,BMG_DS054866,"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT"
+BMGC_DS14329,BMG_DS054867,NESCAV syndrome
+BMGC_DS14330,BMG_DS054868,"intellectual disability, autosomal dominant 10"
+BMGC_DS14331,BMG_DS054869,CHROMOSOME 20q11-q12 DELETION SYNDROME
+BMGC_DS14332,BMG_DS054870,Microcephaly-capillary malformation syndrome
+BMGC_DS14333,BMG_DS054871,"ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY"
+BMGC_DS14334,BMG_DS054872,Combined Malonic and Methylmalonic Aciduria
+BMGC_DS14335,BMG_DS054873,Platelet-Activating Factor Acetylhydrolase Deficiency
+BMGC_DS14336,BMG_DS054874,"epilepsy, juvenile myoclonic, susceptibility to, 9"
+BMGC_DS14337,BMG_DS054875,"STICKLER SYNDROME, TYPE V"
+BMGC_DS14338,BMG_DS054876,"breast-ovarian cancer, familial, susceptibility to, 4"
+BMGC_DS14339,BMG_DS054877,"MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION"
+BMGC_DS14340,BMG_DS054878,"HYDATIDIFORM MOLE, RECURRENT, 2"
+BMGC_DS14341,BMG_DS054879,CHROMOSOME 15q25 DELETION SYNDROME
+BMGC_DS14342,BMG_DS054880,"Wolfram-Like Syndrome, Autosomal Dominant"
+BMGC_DS14343,BMG_DS054881,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4
+BMGC_DS14344,BMG_DS054882,Multiple mitochondrial dysfunctions syndrome type 2
+BMGC_DS14345,BMG_DS054883,EDICT syndrome
+BMGC_DS14346,BMG_DS054885,SCLEROSTEOSIS 2
+BMGC_DS14347,BMG_DS054886,COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA
+BMGC_DS14348,BMG_DS054887,Alpha-Methylacyl-CoA Racemase Deficiency
+BMGC_DS14349,BMG_DS054891,"pancreatic cancer, susceptibility to, 4"
+BMGC_DS14350,BMG_DS054892,"MYOPATHY, DISTAL, TATEYAMA TYPE"
+BMGC_DS14351,BMG_DS054893,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12"
+BMGC_DS14352,BMG_DS054894,OVARIAN DYSGENESIS 3
+BMGC_DS14353,BMG_DS054895,PITT-HOPKINS-LIKE SYNDROME 2
+BMGC_DS14354,BMG_DS054896,FEINGOLD SYNDROME 2
+BMGC_DS14355,BMG_DS054897,TUMOR PREDISPOSITION SYNDROME 1
+BMGC_DS14356,BMG_DS054898,"INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 1"
+BMGC_DS14357,BMG_DS054899,"intellectual disability, autosomal recessive 31"
+BMGC_DS14358,BMG_DS054900,SCHIZOPHRENIA 17
+BMGC_DS14359,BMG_DS054901,"intellectual disability, autosomal recessive 29"
+BMGC_DS14360,BMG_DS054902,"ARTHROGRYPOSIS, DISTAL, TYPE 1B"
+BMGC_DS14361,BMG_DS054903,pancreatic triacylglycerol lipase deficiency
+BMGC_DS14362,BMG_DS054904,"COLIPASE, CONGENITAL ABSENCE OF PANCREATIC"
+BMGC_DS14363,BMG_DS054905,"LIPASE AND COLIPASE, DEFICIENCY OF"
+BMGC_DS14364,BMG_DS054906,"LIPASE AND COLIPASE, CONGENITAL ABSENCE OF PANCREATIC"
+BMGC_DS14365,BMG_DS054907,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 27"
+BMGC_DS14366,BMG_DS054908,"intellectual disability, autosomal recessive 33"
+BMGC_DS14367,BMG_DS054909,"intellectual disability, autosomal recessive 30"
+BMGC_DS14368,BMG_DS054910,"intellectual disability, autosomal recessive 19"
+BMGC_DS14369,BMG_DS054911,"intellectual disability, autosomal recessive 23"
+BMGC_DS14370,BMG_DS054912,"intellectual disability, autosomal recessive 24"
+BMGC_DS14371,BMG_DS054913,"intellectual disability, autosomal recessive 25"
+BMGC_DS14372,BMG_DS054914,"intellectual disability, autosomal recessive 28"
+BMGC_DS14373,BMG_DS054915,"PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS"
+BMGC_DS14374,BMG_DS054916,"SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 5"
+BMGC_DS14375,BMG_DS054917,"dengue virus, susceptibility to"
+BMGC_DS14376,BMG_DS054920,Mannose-Binding Protein Deficiency
+BMGC_DS14377,BMG_DS054921,"AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE"
+BMGC_DS14378,BMG_DS054923,SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY
+BMGC_DS14379,BMG_DS054924,NEPHRONOPHTHISIS 13
+BMGC_DS14380,BMG_DS054925,CRANIOECTODERMAL DYSPLASIA 4
+BMGC_DS14381,BMG_DS054929,complement component 4b deficiency
+BMGC_DS14382,BMG_DS054930,complement component 4a deficiency
+BMGC_DS14383,BMG_DS054931,"LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM"
+BMGC_DS14384,BMG_DS054932,"bacteremia, susceptibility to, 1"
+BMGC_DS14385,BMG_DS054933,"bacteremia, susceptibility"
+BMGC_DS14386,BMG_DS054934,"bacteremia, susceptibility to, 2"
+BMGC_DS14387,BMG_DS054935,ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1
+BMGC_DS14388,BMG_DS054936,"pregnancy loss, recurrent, susceptibility to, 1"
+BMGC_DS14389,BMG_DS054937,"pregnancy loss, recurrent, susceptibility to, 2"
+BMGC_DS14390,BMG_DS054938,"pregnancy loss, recurrent, susceptibility to, 3"
+BMGC_DS14391,BMG_DS054939,"graft-versus-host disease, susceptibility to"
+BMGC_DS14392,BMG_DS054940,"Early-onset myopathy, areflexia, respiratory distress, dysphagia syndrome"
+BMGC_DS14393,BMG_DS054941,"glucocorticoid therapy, response to"
+BMGC_DS14394,BMG_DS054942,"Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome"
+BMGC_DS14395,BMG_DS054943,CHILBLAIN LUPUS 2
+BMGC_DS14396,BMG_DS054945,RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES
+BMGC_DS14397,BMG_DS054946,"EPILEPSY, FAMILIAL TEMPORAL LOBE, 5"
+BMGC_DS14398,BMG_DS054947,"FEBRILE SEIZURES, FAMILIAL, 11"
+BMGC_DS14399,BMG_DS054948,SYSTEMIC LUPUS ERYTHEMATOSUS 16
+BMGC_DS14400,BMG_DS054950,CATARACT 37
+BMGC_DS14401,BMG_DS054951,JOUBERT SYNDROME 14
+BMGC_DS14402,BMG_DS054952,VENTRICULAR SEPTAL DEFECT 1
+BMGC_DS14403,BMG_DS054954,ATRIOVENTRICULAR SEPTAL DEFECT 4
+BMGC_DS14404,BMG_DS054956,ventricular septal defect 2
+BMGC_DS14405,BMG_DS054957,VENTRICULAR SEPTAL DEFECT 3
+BMGC_DS14406,BMG_DS054959,atrial septal defect 8
+BMGC_DS14407,BMG_DS054961,"CUTIS LAXA, AUTOSOMAL DOMINANT 2"
+BMGC_DS14408,BMG_DS054962,HYPOPLASTIC LEFT HEART SYNDROME 2
+BMGC_DS14409,BMG_DS054963,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P"
+BMGC_DS14410,BMG_DS054964,"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB"
+BMGC_DS14411,BMG_DS054965,Pyrroline-5-carboxylate reductase 1 related de Barsy syndrome
+BMGC_DS14412,BMG_DS054966,"HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2"
+BMGC_DS14413,BMG_DS054967,"HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6"
+BMGC_DS14414,BMG_DS054968,"Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome"
+BMGC_DS14415,BMG_DS054969,THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)
+BMGC_DS14416,BMG_DS054970,"HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES"
+BMGC_DS14417,BMG_DS054971,JOUBERT SYNDROME 15
+BMGC_DS14418,BMG_DS054972,"JOUBERT SYNDROME 9/15, DIGENIC"
+BMGC_DS14419,BMG_DS054973,"JOUBERT SYNDROME 12/15, DIGENIC"
+BMGC_DS14420,BMG_DS054974,JOUBERT SYNDROME 16
+BMGC_DS14421,BMG_DS054975,"coronary heart disease, susceptibility to, 6"
+BMGC_DS14422,BMG_DS054976,FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3
+BMGC_DS14423,BMG_DS054977,ATRIOVENTRICULAR SEPTAL DEFECT 5
+BMGC_DS14424,BMG_DS054978,ATRIAL SEPTAL DEFECT 9
+BMGC_DS14425,BMG_DS054979,"HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE"
+BMGC_DS14426,BMG_DS054980,BRAIN SMALL VESSEL DISEASE 2
+BMGC_DS14427,BMG_DS054981,trigonocephaly 2
+BMGC_DS14428,BMG_DS054982,Thrombophilia due to Thrombomodulin Defect
+BMGC_DS14429,BMG_DS054983,"SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE"
+BMGC_DS14430,BMG_DS054985,WISKOTT-ALDRICH SYNDROME 2
+BMGC_DS14431,BMG_DS054986,RETINITIS PIGMENTOSA 63
+BMGC_DS14432,BMG_DS054987,MICROPHTHALMIA/COLOBOMA 7
+BMGC_DS14433,BMG_DS054988,"Lethal neonatal spasticity, epileptic encephalopathy syndrome"
+BMGC_DS14434,BMG_DS054989,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY"
+BMGC_DS14435,BMG_DS054990,CONE-ROD DYSTROPHY 16
+BMGC_DS14436,BMG_DS054991,RETINITIS PIGMENTOSA 64
+BMGC_DS14437,BMG_DS054992,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, CRANIOFACIAL ABNORMALITIES, AND SEIZURES"
+BMGC_DS14438,BMG_DS054993,"USHER SYNDROME, TYPE IIIB"
+BMGC_DS14439,BMG_DS054994,Congenital disorder of glycosylation type 1r
+BMGC_DS14440,BMG_DS054995,MIRROR MOVEMENTS 2
+BMGC_DS14441,BMG_DS054996,"THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE"
+BMGC_DS14442,BMG_DS054997,"hemorrhage, intracerebral, susceptibility to"
+BMGC_DS14443,BMG_DS054998,"ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY"
+BMGC_DS14444,BMG_DS055000,THROMBOCYTHEMIA 3
+BMGC_DS14445,BMG_DS055001,FIBROCHONDROGENESIS 2
+BMGC_DS14446,BMG_DS055002,17q12 microduplication syndrome
+BMGC_DS14447,BMG_DS055003,CHROMOSOME 17q12 DELETION SYNDROME
+BMGC_DS14448,BMG_DS055004,CHROMOSOME 16q22 DELETION SYNDROME
+BMGC_DS14449,BMG_DS055005,"efavirenz central nervous system toxicity, susceptibility to"
+BMGC_DS14450,BMG_DS055006,"EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2"
+BMGC_DS14451,BMG_DS055008,SCN8A-related epilepsy with encephalopathy
+BMGC_DS14452,BMG_DS055009,Infantile cerebellar and retinal degeneration
+BMGC_DS14453,BMG_DS055010,Leukoencephalopathy Brain Calcifications and Cysts
+BMGC_DS14454,BMG_DS055011,COFFIN-SIRIS SYNDROME 1
+BMGC_DS14455,BMG_DS055012,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 13"
+BMGC_DS14456,BMG_DS055013,familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
+BMGC_DS14457,BMG_DS055014,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E"
+BMGC_DS14458,BMG_DS055016,"CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME"
+BMGC_DS14459,BMG_DS055017,BARAITSER-WINTER SYNDROME 2
+BMGC_DS14460,BMG_DS055018,DYSTONIA 21
+BMGC_DS14461,BMG_DS055020,BENT BONE DYSPLASIA SYNDROME 1
+BMGC_DS14462,BMG_DS055027,PREECLAMPSIA/ECLAMPSIA 5
+BMGC_DS14463,BMG_DS055028,TRICHOHEPATOENTERIC SYNDROME 2
+BMGC_DS14464,BMG_DS055029,"DEAFNESS, AUTOSOMAL DOMINANT 4B"
+BMGC_DS14465,BMG_DS055032,myelodysplastic syndrome
+BMGC_DS14466,BMG_DS055033,"HYDATIDIFORM MOLE, RECURRENT, 1"
+BMGC_DS14467,BMG_DS055035,Complement Factor I Deficiency
+BMGC_DS14468,BMG_DS055036,corticosterone methyloxidase type 2 deficiency
+BMGC_DS14469,BMG_DS055037,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1"
+BMGC_DS14470,BMG_DS055038,"FANCONI ANEMIA, COMPLEMENTATION GROUP C"
+BMGC_DS14471,BMG_DS055040,Juvenile amyotrophic lateral sclerosis
+BMGC_DS14472,BMG_DS055044,familial atrial fibrillation
+BMGC_DS14473,BMG_DS055059,"HEMOCHROMATOSIS, TYPE 1"
+BMGC_DS14474,BMG_DS055061,Fanconi anemia complementation group A
+BMGC_DS14475,BMG_DS055062,"FANCONI ANEMIA, COMPLEMENTATION GROUP F"
+BMGC_DS14476,BMG_DS055063,Fanconi anemia complementation group G
+BMGC_DS14477,BMG_DS055064,"FANCONI ANEMIA, COMPLEMENTATION GROUP L"
+BMGC_DS14478,BMG_DS055065,"FANCONI ANEMIA, COMPLEMENTATION GROUP P"
+BMGC_DS14479,BMG_DS055066,"PSEUDOHYPOALDOSTERONISM, TYPE IID"
+BMGC_DS14480,BMG_DS055067,"PSEUDOHYPOALDOSTERONISM, TYPE IIE"
+BMGC_DS14481,BMG_DS055071,Severe dehydration
+BMGC_DS14482,BMG_DS055080,myeloid neoplasm associated with PDGFRB rearrangement
+BMGC_DS14483,BMG_DS055095,Spinocerebellar ataxia 36
+BMGC_DS14484,BMG_DS055096,HERMANSKY-PUDLAK SYNDROME 4
+BMGC_DS14485,BMG_DS055097,hiatus hernia
+BMGC_DS14486,BMG_DS055098,"Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial"
+BMGC_DS14487,BMG_DS055099,"Hypogonadism, Isolated Hypogonadotropic"
+BMGC_DS14488,BMG_DS055102,Hyperkalemic Periodic Paralysis Type 2
+BMGC_DS14489,BMG_DS055103,"tooth agenesis, selective, 1"
+BMGC_DS14490,BMG_DS055104,Cone-Rod Dystrophy 2
+BMGC_DS14491,BMG_DS055106,"Stuttering, Familial Persistent 1"
+BMGC_DS14492,BMG_DS055107,"Thrombocytosis, Autosomal Dominant"
+BMGC_DS14493,BMG_DS055108,Vision Disability
+BMGC_DS14494,BMG_DS055109,Aicardi-Goutieres Syndrome 2
+BMGC_DS14495,BMG_DS055110,Pseudo-TORCH syndrome
+BMGC_DS14496,BMG_DS055111,geleophysic dysplasia
+BMGC_DS14497,BMG_DS055113,Familial intrahepatic cholestasis of pregnancy
+BMGC_DS14498,BMG_DS055114,Familial mesangial sclerosis
+BMGC_DS14499,BMG_DS055115,Oculomotor apraxia
+BMGC_DS14500,BMG_DS055116,"Anti-plasmin deficiency, congenital"
+BMGC_DS14501,BMG_DS055118,"Pituitary Hormone Deficiency, Combined, 3"
+BMGC_DS14502,BMG_DS055120,progressive familial intrahepatic cholestasis type 2
+BMGC_DS14503,BMG_DS055123,"46,XY sex reversal 3"
+BMGC_DS14504,BMG_DS055125,"Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant"
+BMGC_DS14505,BMG_DS055126,"Thyroid Hormone Resistance, Generalized, Autosomal Recessive"
+BMGC_DS14506,BMG_DS055129,Lentiginosis Profusa
+BMGC_DS14507,BMG_DS055130,"HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1"
+BMGC_DS14508,BMG_DS055131,Endemic Elephantiasis
+BMGC_DS14509,BMG_DS055132,Endemic Non-Filarial Elephantiasis
+BMGC_DS14510,BMG_DS055133,Bigfoot Disease
+BMGC_DS14511,BMG_DS055134,"Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous"
+BMGC_DS14512,BMG_DS055135,fused mandibular incisors
+BMGC_DS14513,BMG_DS055136,paragangliomas 1
+BMGC_DS14514,BMG_DS055137,Autosomal Hemophilia A
+BMGC_DS14515,BMG_DS055138,Factor VIII Deficiency
+BMGC_DS14516,BMG_DS055145,"Autoimmune polyendocrinopathy syndrome, type 1"
+BMGC_DS14517,BMG_DS055146,"Pseudohypoparathyroidism, Type Ia"
+BMGC_DS14518,BMG_DS055147,"Hypergonadotropic Ovarian Failure, X-Linked"
+BMGC_DS14519,BMG_DS055228,benign paroxysmal torticollis of infancy
+BMGC_DS14520,BMG_DS055239,Malignant migrating partial seizures of infancy (disorder)
+BMGC_DS14521,BMG_DS055261,familial ossifying fibroma
+BMGC_DS14522,BMG_DS055264,craniofacial microsomia 1
+BMGC_DS14523,BMG_DS055265,Chromosome 18q syndrome
+BMGC_DS14524,BMG_DS055267,Fanconi-Bickel Syndrome
+BMGC_DS14525,BMG_DS055269,"Macular Degeneration, Age-Related, 2"
+BMGC_DS14526,BMG_DS055272,Amish Brittle Hair Brain Syndrome
+BMGC_DS14527,BMG_DS055273,Axenfeld-Rieger syndrome
+BMGC_DS14528,BMG_DS055275,Acrorenal Syndrome
+BMGC_DS14529,BMG_DS055276,"Cardiomyopathy, Familial Hypertrophic, 1"
+BMGC_DS14530,BMG_DS055279,"heterotaxy, visceral, 5, autosomal"
+BMGC_DS14531,BMG_DS055282,Dihydropyrimidinuria
+BMGC_DS14532,BMG_DS055284,Homocarnosinase deficiency
+BMGC_DS14533,BMG_DS055285,Carnosinemia
+BMGC_DS14534,BMG_DS055287,Juvenile arthritis
+BMGC_DS14535,BMG_DS055289,"Night Blindness, Congenital Stationary, Type 1A"
+BMGC_DS14536,BMG_DS055290,Acrocephalopolydactylous Dysplasia
+BMGC_DS14537,BMG_DS055291,Jalili syndrome
+BMGC_DS14538,BMG_DS055293,"Charcot-Marie-Tooth Disease, Demyelinating, Type 1e"
+BMGC_DS14539,BMG_DS055295,hereditary anorectal anomalies
+BMGC_DS14540,BMG_DS055296,NF1 Microduplication Syndrome
+BMGC_DS14541,BMG_DS055298,Granulomatosis with polyangiitis
+BMGC_DS14542,BMG_DS055300,Nonepileptic Seizures
+BMGC_DS14543,BMG_DS055304,"Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia"
+BMGC_DS14544,BMG_DS055306,idiopathic nephrotic syndrome
+BMGC_DS14545,BMG_DS055307,Middle aortic syndrome
+BMGC_DS14546,BMG_DS055308,Parkinson Disease 13
+BMGC_DS14547,BMG_DS055311,"Nephrotic Syndrome, Congenital, With Ocular Abnormalities And Congenital Myasthenic Syndrome"
+BMGC_DS14548,BMG_DS055312,"Deafness, Sensorineural, with Hypertrophic Cardiomyopathy"
+BMGC_DS14549,BMG_DS055314,"Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosomal Recessive"
+BMGC_DS14550,BMG_DS055316,Mental Retardation associated with Psoriasis
+BMGC_DS14551,BMG_DS055319,"Mental Retardation, X-Linked Nonsyndromic"
+BMGC_DS14552,BMG_DS055320,"Generalized Epilepsy With Febrile Seizures Plus, Type 5"
+BMGC_DS14553,BMG_DS055321,"Glutathione Peroxidase Deficiency, Hemolytic Anemia possibly due to"
+BMGC_DS14554,BMG_DS055324,Bleeding Disorder due to Defective Thromboxane A2 Receptor
+BMGC_DS14555,BMG_DS055326,T-Cell OKT4 Deficiency
+BMGC_DS14556,BMG_DS055337,"Microcephaly, Primary Autosomal Recessive, 2"
+BMGC_DS14557,BMG_DS055345,"Night blindness, congenital stationary, type 1"
+BMGC_DS14558,BMG_DS055346,"Nephrosis, congenital"
+BMGC_DS14559,BMG_DS055347,Mngie Without Leukoencephalopathy
+BMGC_DS14560,BMG_DS055352,"leukemia, acute, X-linked"
+BMGC_DS14561,BMG_DS055355,"Muscular Dystrophy, Limb-Girdle, Type 1D"
+BMGC_DS14562,BMG_DS055357,"Mitochondrial DNA Depletion Syndrome, Myopathic Form"
+BMGC_DS14563,BMG_DS055362,Cerebrocostomandibular-Like Syndrome
+BMGC_DS14564,BMG_DS055371,"Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive"
+BMGC_DS14565,BMG_DS055372,"Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant"
+BMGC_DS14566,BMG_DS055373,"Leukodystrophy, Dysmyelinating, with Oligodontia"
+BMGC_DS14567,BMG_DS055378,"Woolly Hair, Autosomal Recessive"
+BMGC_DS14568,BMG_DS055379,Multiple Mitochondrial Dysfunctions Syndrome
+BMGC_DS14569,BMG_DS055380,"Dyskeratosis Congenita, Autosomal Recessive"
+BMGC_DS14570,BMG_DS055385,"Homocystinuria, Pyridoxine-Responsive"
+BMGC_DS14571,BMG_DS055386,"Adrenal Insufficiency, Congenital"
+BMGC_DS14572,BMG_DS055387,"Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal"
+BMGC_DS14573,BMG_DS055394,Microcephalic Osteodysplastic Primordial Dwarfism with Tooth Abnormalities
+BMGC_DS14574,BMG_DS055400,"Deafness, Autosomal Recessive 36, Without Vestibular Involvement"
+BMGC_DS14575,BMG_DS055406,Atresia of External Auditory Canal and Conduction Deafness
+BMGC_DS14576,BMG_DS055419,"Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia"
+BMGC_DS14577,BMG_DS055420,"Microcephaly with Chorioretinopathy, Autosomal Recessive"
+BMGC_DS14578,BMG_DS055421,Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal
+BMGC_DS14579,BMG_DS055432,Generalized Epilepsy with Febrile Seizures Plus
+BMGC_DS14580,BMG_DS055463,Ehlers-Danlos syndrome type 7A
+BMGC_DS14581,BMG_DS055638,Mitochondrial cardiomyopathy
+BMGC_DS14582,BMG_DS055642,Fatal infantile mitochondrial cardiomyopathy
+BMGC_DS14583,BMG_DS055645,Fetal cardiomyopathy
+BMGC_DS14584,BMG_DS055736,renal dysplasia
+BMGC_DS14585,BMG_DS055737,AA amyloidosis
+BMGC_DS14586,BMG_DS055738,Secondary systemic amyloidosis
+BMGC_DS14587,BMG_DS055741,Ichthyosis Congenita II
+BMGC_DS14588,BMG_DS055746,Familial Hypophosphatemic Rickets
+BMGC_DS14589,BMG_DS055747,"Vitamin D-Resistant Rickets, X-Linked"
+BMGC_DS14590,BMG_DS055748,inferolateral myocardial infarct
+BMGC_DS14591,BMG_DS055749,Ménière's Vertigo
+BMGC_DS14592,BMG_DS055752,"Cystinosis, Infantile Nephropathic"
+BMGC_DS14593,BMG_DS055753,"Kaposi sarcoma, susceptibility to"
+BMGC_DS14594,BMG_DS055754,"DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT"
+BMGC_DS14595,BMG_DS055755,"MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA"
+BMGC_DS14596,BMG_DS055756,DYSTONIA 23
+BMGC_DS14597,BMG_DS055757,Hereditary sensory and autonomic neuropathy type 6
+BMGC_DS14598,BMG_DS055758,"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP F"
+BMGC_DS14599,BMG_DS055759,AICARDI-GOUTIERES SYNDROME 6
+BMGC_DS14600,BMG_DS055760,NEPHRONOPHTHISIS 14
+BMGC_DS14601,BMG_DS055761,"prostate cancer, hereditary, 2"
+BMGC_DS14602,BMG_DS055762,"CEROID LIPOFUSCINOSIS, NEURONAL, 11"
+BMGC_DS14603,BMG_DS055763,"USHER SYNDROME, TYPE IK"
+BMGC_DS14604,BMG_DS055764,"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A"
+BMGC_DS14605,BMG_DS055765,"TREMOR, HEREDITARY ESSENTIAL, 4"
+BMGC_DS14606,BMG_DS055766,"SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE"
+BMGC_DS14607,BMG_DS055767,"SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE"
+BMGC_DS14608,BMG_DS055768,"SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE"
+BMGC_DS14609,BMG_DS055769,"SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE"
+BMGC_DS14610,BMG_DS055770,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3"
+BMGC_DS14611,BMG_DS055771,"MYOCLONUS, FAMILIAL CORTICAL"
+BMGC_DS14612,BMG_DS055772,"ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE"
+BMGC_DS14613,BMG_DS055773,HYPOGONADOTROPIC HYPOGONADISM 14 WITH OR WITHOUT ANOSMIA
+BMGC_DS14614,BMG_DS055774,"CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F"
+BMGC_DS14615,BMG_DS055775,Congenital Amaurosis of Retinal Origin
+BMGC_DS14616,BMG_DS055776,"CILIARY DYSKINESIA, PRIMARY, 20"
+BMGC_DS14617,BMG_DS055777,"MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 8"
+BMGC_DS14618,BMG_DS055778,"CATARACT 4, MULTIPLE TYPES"
+BMGC_DS14619,BMG_DS055779,"Rickets, X-Linked Hypophosphatemic"
+BMGC_DS14620,BMG_DS055780,"SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY"
+BMGC_DS14621,BMG_DS055781,PONTINE TEGMENTAL CAP DYSPLASIA
+BMGC_DS14622,BMG_DS055783,"spondyloepiphyseal dysplasia tarda, X-linked"
+BMGC_DS14623,BMG_DS055786,HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA
+BMGC_DS14624,BMG_DS055787,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1"
+BMGC_DS14625,BMG_DS055788,"ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE"
+BMGC_DS14626,BMG_DS055789,"MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET, MILD VARIANT"
+BMGC_DS14627,BMG_DS055790,"ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT"
+BMGC_DS14628,BMG_DS055791,"ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT"
+BMGC_DS14629,BMG_DS055792,NEPHRONOPHTHISIS 15
+BMGC_DS14630,BMG_DS055793,Drug Hypersensitivity Syndrome
+BMGC_DS14631,BMG_DS055794,Duchenne and Becker Muscular Dystrophy
+BMGC_DS14632,BMG_DS055795,"Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome"
+BMGC_DS14633,BMG_DS055796,AORTIC VALVE DISEASE 2
+BMGC_DS14634,BMG_DS055797,"AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE"
+BMGC_DS14635,BMG_DS055798,PEROXISOME BIOGENESIS DISORDER 5B
+BMGC_DS14636,BMG_DS055799,Aminoacylase 2 Deficiency
+BMGC_DS14637,BMG_DS055800,ADH-Resistant Diabetes Insipidus
+BMGC_DS14638,BMG_DS055801,"NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IX, WITH DEVELOPMENTAL DELAY"
+BMGC_DS14639,BMG_DS055802,"CILIARY DYSKINESIA, PRIMARY, 17"
+BMGC_DS14640,BMG_DS055803,"IMMUNODEFICIENCY, COMMON VARIABLE, 7"
+BMGC_DS14641,BMG_DS055805,"CILIARY DYSKINESIA, PRIMARY, 18"
+BMGC_DS14642,BMG_DS055806,"CILIARY DYSKINESIA, PRIMARY, 19"
+BMGC_DS14643,BMG_DS055809,Collodion Fetus
+BMGC_DS14644,BMG_DS055815,treatment-refractory schizophrenia
+BMGC_DS14645,BMG_DS055818,ALTERNATING HEMIPLEGIA OF CHILDHOOD 1
+BMGC_DS14646,BMG_DS055819,NOR POLYAGGLUTINATION SYNDROME
+BMGC_DS14647,BMG_DS055820,ACAMPOMELIC CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL
+BMGC_DS14648,BMG_DS055826,"CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1"
+BMGC_DS14649,BMG_DS055827,"MACROGLOBULINEMIA, WALDENSTROM, SOMATIC"
+BMGC_DS14650,BMG_DS055829,METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA WITH OR WITHOUT BRACHYDACTYLY
+BMGC_DS14651,BMG_DS055831,peroxisome biogenesis disorder 2B
+BMGC_DS14652,BMG_DS055832,peroxisome biogenesis disorder 2A (Zellweger)
+BMGC_DS14653,BMG_DS055833,"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 2"
+BMGC_DS14654,BMG_DS055836,"HYPERBILIRUBINEMIA, SHUNT, PRIMARY"
+BMGC_DS14655,BMG_DS055841,HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA
+BMGC_DS14656,BMG_DS055843,"POLYDACTYLY, POSTAXIAL, TYPE A5"
+BMGC_DS14657,BMG_DS055844,PEROXISOME BIOGENESIS DISORDER 3B
+BMGC_DS14658,BMG_DS055846,"THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA"
+BMGC_DS14659,BMG_DS055847,"ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES"
+BMGC_DS14660,BMG_DS055849,"AUTISM, SUSCEPTIBILITY TO, X-LINKED 6"
+BMGC_DS14661,BMG_DS055850,CORNELIA DE LANGE SYNDROME 5
+BMGC_DS14662,BMG_DS055851,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 32"
+BMGC_DS14663,BMG_DS055852,LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2
+BMGC_DS14664,BMG_DS055854,"HYPOTHYROIDISM, CENTRAL, WITH TESTICULAR ENLARGEMENT"
+BMGC_DS14665,BMG_DS055855,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5
+BMGC_DS14666,BMG_DS055856,CHROMOSOME Xq21 DELETION SYNDROME
+BMGC_DS14667,BMG_DS055860,"PAROTID SALIVARY GLANDS, POLYCYSTIC DYSGENETIC DISEASE OF"
+BMGC_DS14668,BMG_DS055861,UV-SENSITIVE SYNDROME 1
+BMGC_DS14669,BMG_DS055863,"ECTODERMAL DYSPLASIA 8, HAIR/TOOTH/NAIL TYPE"
+BMGC_DS14670,BMG_DS055864,ANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT
+BMGC_DS14671,BMG_DS055866,CORTISONE REDUCTASE DEFICIENCY 1
+BMGC_DS14672,BMG_DS055868,familial meningioma
+BMGC_DS14673,BMG_DS055869,"COENZYME Q10 DEFICIENCY, PRIMARY, 1"
+BMGC_DS14674,BMG_DS055870,ACHROMATOPSIA 6
+BMGC_DS14675,BMG_DS055871,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7"
+BMGC_DS14676,BMG_DS055873,"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH MILD PALMOPLANTAR KERATODERMA AND WOOLLY HAIR"
+BMGC_DS14677,BMG_DS055874,"MYASTHENIC SYNDROME, CONGENITAL, 12"
+BMGC_DS14678,BMG_DS055875,HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA
+BMGC_DS14679,BMG_DS055883,HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA
+BMGC_DS14680,BMG_DS055884,HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA
+BMGC_DS14681,BMG_DS055885,LYMPHOPROLIFERATIVE SYNDROME 1
+BMGC_DS14682,BMG_DS055886,RETINITIS PIGMENTOSA 65
+BMGC_DS14683,BMG_DS055888,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8"
+BMGC_DS14684,BMG_DS055889,"EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT"
+BMGC_DS14685,BMG_DS055890,"MICROPHTHALMIA, SYNDROMIC 11"
+BMGC_DS14686,BMG_DS055893,COG6-CGD - component of oligomeric golgi complex 6-congenital disorder of glycosylation
+BMGC_DS14687,BMG_DS055894,COFFIN-SIRIS SYNDROME 2
+BMGC_DS14688,BMG_DS055895,COFFIN-SIRIS SYNDROME 3
+BMGC_DS14689,BMG_DS055896,COFFIN-SIRIS SYNDROME 4
+BMGC_DS14690,BMG_DS055897,ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE
+BMGC_DS14691,BMG_DS055898,JOUBERT SYNDROME 17
+BMGC_DS14692,BMG_DS055899,DIARRHEA 6
+BMGC_DS14693,BMG_DS055907,HYPEREKPLEXIA 3
+BMGC_DS14694,BMG_DS055908,HYPEREKPLEXIA 2
+BMGC_DS14695,BMG_DS055909,UV-SENSITIVE SYNDROME 2
+BMGC_DS14696,BMG_DS055910,KERATOCONUS 5
+BMGC_DS14697,BMG_DS055911,KERATOCONUS 6
+BMGC_DS14698,BMG_DS055912,KERATOCONUS 8
+BMGC_DS14699,BMG_DS055913,KERATOCONUS 7
+BMGC_DS14700,BMG_DS055914,UV-SENSITIVE SYNDROME 3
+BMGC_DS14701,BMG_DS055915,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7"
+BMGC_DS14702,BMG_DS055916,"COENZYME Q10 DEFICIENCY, PRIMARY, 6"
+BMGC_DS14703,BMG_DS055917,"COENZYME Q10 DEFICIENCY, PRIMARY, 2"
+BMGC_DS14704,BMG_DS055918,"COENZYME Q10 DEFICIENCY, PRIMARY, 3"
+BMGC_DS14705,BMG_DS055919,"COENZYME Q10 DEFICIENCY, PRIMARY, 5"
+BMGC_DS14706,BMG_DS055921,CORTISONE REDUCTASE DEFICIENCY 2
+BMGC_DS14707,BMG_DS055923,"STUTTERING, FAMILIAL PERSISTENT, 4"
+BMGC_DS14708,BMG_DS055924,AURICULOCONDYLAR SYNDROME 2A
+BMGC_DS14709,BMG_DS055926,CHROMOSOME 16p11.2 DUPLICATION SYNDROME
+BMGC_DS14710,BMG_DS055928,"CARDIOMYOPATHY, DILATED, 2B"
+BMGC_DS14711,BMG_DS055929,"MICROCEPHALY 8, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS14712,BMG_DS055930,Menstrual cycle dependent periodic fever
+BMGC_DS14713,BMG_DS055932,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21"
+BMGC_DS14714,BMG_DS055933,"PONTOCEREBELLAR HYPOPLASIA, TYPE 1B"
+BMGC_DS14715,BMG_DS055934,Profound global developmental delay
+BMGC_DS14716,BMG_DS055935,"influenza, severe, susceptibility to"
+BMGC_DS14717,BMG_DS055936,"HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, IMPAIRED INTELLECTUAL DEVELOPMENT, AND RECURRENT INFLAMMATORY EPISODES"
+BMGC_DS14718,BMG_DS055938,"ALAR CLEFT, ISOLATED"
+BMGC_DS14719,BMG_DS055939,CATARACT 38
+BMGC_DS14720,BMG_DS055940,"IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY"
+BMGC_DS14721,BMG_DS055941,CORNELIA DE LANGE SYNDROME 4
+BMGC_DS14722,BMG_DS055942,Brown-Vialetto-van Laere syndrome 2
+BMGC_DS14723,BMG_DS055943,"POROKERATOSIS 7, MULTIPLE TYPES"
+BMGC_DS14724,BMG_DS055944,Carbohydrate deficient glycoprotein syndrome type 2k
+BMGC_DS14725,BMG_DS055945,SECKEL SYNDROME 6
+BMGC_DS14726,BMG_DS055946,GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY
+BMGC_DS14727,BMG_DS055947,"basal cell carcinoma, susceptibility to, 7"
+BMGC_DS14728,BMG_DS055948,Mitochondrial pyruvate carrier deficiency
+BMGC_DS14729,BMG_DS055949,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 1"
+BMGC_DS14730,BMG_DS055950,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 2"
+BMGC_DS14731,BMG_DS055951,"FACIAL PARESIS, HEREDITARY CONGENITAL, 3"
+BMGC_DS14732,BMG_DS055952,HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 2
+BMGC_DS14733,BMG_DS055953,"MYASTHENIC SYNDROME, CONGENITAL, 13"
+BMGC_DS14734,BMG_DS055954,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 12"
+BMGC_DS14735,BMG_DS055955,Malan overgrowth syndrome
+BMGC_DS14736,BMG_DS055956,CEREBELLAR DYSFUNCTION WITH VARIABLE COGNITIVE AND BEHAVIORAL ABNORMALITIES
+BMGC_DS14737,BMG_DS055957,"HETEROTAXY, VISCERAL, 6, AUTOSOMAL"
+BMGC_DS14738,BMG_DS055958,AMYOTROPHIC LATERAL SCLEROSIS 18
+BMGC_DS14739,BMG_DS055959,C3 GLOMERULOPATHY 3
+BMGC_DS14740,BMG_DS055960,"multiple sclerosis, susceptibility to, 5"
+BMGC_DS14741,BMG_DS055961,ADAMS-OLIVER SYNDROME 3
+BMGC_DS14742,BMG_DS055962,JOUBERT SYNDROME 18
+BMGC_DS14743,BMG_DS055963,LOEYS-DIETZ SYNDROME 4
+BMGC_DS14744,BMG_DS055964,"INTERSTITIAL NEPHRITIS, KARYOMEGALIC"
+BMGC_DS14745,BMG_DS055966,WEILL-MARCHESANI SYNDROME 3
+BMGC_DS14746,BMG_DS055967,ALTERNATING HEMIPLEGIA OF CHILDHOOD 2
+BMGC_DS14747,BMG_DS055968,SPERMATOGENIC FAILURE 10
+BMGC_DS14748,BMG_DS055969,spermatogenic failure
+BMGC_DS14749,BMG_DS055970,"NYSTAGMUS 7, CONGENITAL, AUTOSOMAL DOMINANT"
+BMGC_DS14750,BMG_DS055971,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8"
+BMGC_DS14751,BMG_DS055972,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13"
+BMGC_DS14752,BMG_DS055973,"AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4"
+BMGC_DS14753,BMG_DS055974,"MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES"
+BMGC_DS14754,BMG_DS055977,HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA
+BMGC_DS14755,BMG_DS055978,HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA
+BMGC_DS14756,BMG_DS055979,HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA
+BMGC_DS14757,BMG_DS055980,HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA
+BMGC_DS14758,BMG_DS055981,JOUBERT SYNDROME 19
+BMGC_DS14759,BMG_DS055982,TETRASOMY 15q26
+BMGC_DS14760,BMG_DS055983,"epilepsy, idiopathic generalized, susceptibility to, 12"
+BMGC_DS14761,BMG_DS055984,"herpes simplex encephalitis, susceptibility to, 3"
+BMGC_DS14762,BMG_DS055985,"herpes simplex encephalitis, susceptibility to, 4"
+BMGC_DS14763,BMG_DS055986,SECKEL SYNDROME 7
+BMGC_DS14764,BMG_DS055987,"MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS14765,BMG_DS055988,"OSTEOGENESIS IMPERFECTA, TYPE XIII"
+BMGC_DS14766,BMG_DS055989,"methylmalonic acidemia with homocystinuria, type cblJ"
+BMGC_DS14767,BMG_DS055990,peroxisome biogenesis disorder 3A (Zellweger)
+BMGC_DS14768,BMG_DS055991,"DEAFNESS, AUTOSOMAL RECESSIVE 98"
+BMGC_DS14769,BMG_DS055992,peroxisome biogenesis disorder 4A (Zellweger)
+BMGC_DS14770,BMG_DS055993,PEROXISOME BIOGENESIS DISORDER 4B
+BMGC_DS14771,BMG_DS055994,peroxisome biogenesis disorder 5A (Zellweger)
+BMGC_DS14772,BMG_DS055995,"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 5"
+BMGC_DS14773,BMG_DS055996,"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 10"
+BMGC_DS14774,BMG_DS055997,IMMUNODEFICIENCY 110 WITH LYMPHOPROLIFERATION
+BMGC_DS14775,BMG_DS055998,"USHER SYNDROME, TYPE IJ"
+BMGC_DS14776,BMG_DS055999,peroxisome biogenesis disorder 6A (Zellweger)
+BMGC_DS14777,BMG_DS056000,peroxisome biogenesis disorder 6B
+BMGC_DS14778,BMG_DS056001,"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 8"
+BMGC_DS14779,BMG_DS056002,peroxisome biogenesis disorder 7B
+BMGC_DS14780,BMG_DS056003,METAPHYSEAL ENCHONDROMATOSIS WITH D-2-HYDROXYGLUTARIC ACIDURIA
+BMGC_DS14781,BMG_DS056004,peroxisome biogenesis disorder 8A (Zellweger)
+BMGC_DS14782,BMG_DS056005,peroxisome biogenesis disorder 8B
+BMGC_DS14783,BMG_DS056006,"AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED"
+BMGC_DS14784,BMG_DS056007,HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA
+BMGC_DS14785,BMG_DS056010,PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER)
+BMGC_DS14786,BMG_DS056011,PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)
+BMGC_DS14787,BMG_DS056012,PEROXISOME BIOGENESIS DISORDER 11B
+BMGC_DS14788,BMG_DS056013,PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)
+BMGC_DS14789,BMG_DS056014,PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)
+BMGC_DS14790,BMG_DS056015,SINOATRIAL NODE DYSFUNCTION AND DEAFNESS
+BMGC_DS14791,BMG_DS056016,HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
+BMGC_DS14792,BMG_DS056017,DIAMOND-BLACKFAN ANEMIA 11
+BMGC_DS14793,BMG_DS056018,LETHAL CONGENITAL CONTRACTURE SYNDROME 4
+BMGC_DS14794,BMG_DS056019,"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4"
+BMGC_DS14795,BMG_DS056020,PEROXISOME BIOGENESIS DISORDER 14B
+BMGC_DS14796,BMG_DS056021,BRANCHED-CHAIN KETO ACID DEHYDROGENASE KINASE DEFICIENCY
+BMGC_DS14797,BMG_DS056022,PERRAULT SYNDROME 2
+BMGC_DS14798,BMG_DS056023,"ECTODERMAL DYSPLASIA 5, HAIR/NAIL TYPE"
+BMGC_DS14799,BMG_DS056024,"ECTODERMAL DYSPLASIA 6, HAIR/NAIL TYPE"
+BMGC_DS14800,BMG_DS056025,"ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE"
+BMGC_DS14801,BMG_DS056026,"ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE"
+BMGC_DS14802,BMG_DS056027,"PALMOPLANTAR KERATODERMA, PUNCTATE TYPE IB"
+BMGC_DS14803,BMG_DS056028,"DEAFNESS, AUTOSOMAL RECESSIVE 84B"
+BMGC_DS14804,BMG_DS056029,"DEAFNESS, AUTOSOMAL RECESSIVE 18B"
+BMGC_DS14805,BMG_DS056030,"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3"
+BMGC_DS14806,BMG_DS056031,"developmental and epileptic encephalopathy, 14"
+BMGC_DS14807,BMG_DS056032,Congenital pontocerebellar hypoplasia type 8
+BMGC_DS14808,BMG_DS056033,LEPTIN DEFICIENCY OR DYSFUNCTION
+BMGC_DS14809,BMG_DS056034,LEPTIN RECEPTOR DEFICIENCY
+BMGC_DS14810,BMG_DS056035,Congenital pontocerebellar hypoplasia type 7
+BMGC_DS14811,BMG_DS056036,JOUBERT SYNDROME 20
+BMGC_DS14812,BMG_DS056037,"CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3"
+BMGC_DS14813,BMG_DS056038,Focal Facial Dermal Dysplasia 2
+BMGC_DS14814,BMG_DS056039,Focal Facial Dermal Dysplasia 4
+BMGC_DS14815,BMG_DS056040,CARPENTER SYNDROME 2
+BMGC_DS14816,BMG_DS056041,"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2"
+BMGC_DS14817,BMG_DS056042,"EPILEPSY, NOCTURNAL FRONTAL LOBE, 5"
+BMGC_DS14818,BMG_DS056043,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 15
+BMGC_DS14819,BMG_DS056044,"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4"
+BMGC_DS14820,BMG_DS056045,"NEPHROTIC SYNDROME, TYPE 7"
+BMGC_DS14821,BMG_DS056046,Schuurs-Hoeijmakers syndrome
+BMGC_DS14822,BMG_DS056047,phosphohydroxylysinuria
+BMGC_DS14823,BMG_DS056048,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 7"
+BMGC_DS14824,BMG_DS056049,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 9"
+BMGC_DS14825,BMG_DS056050,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10"
+BMGC_DS14826,BMG_DS056051,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q"
+BMGC_DS14827,BMG_DS056052,"EPIDERMOLYSIS BULLOSA SIMPLEX 4, LOCALIZED OR GENERALIZED INTERMEDIATE, AUTOSOMAL RECESSIVE"
+BMGC_DS14828,BMG_DS056053,INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND MACROCEPHALY
+BMGC_DS14829,BMG_DS056054,Cranio-cervical dystonia with laryngeal and upper limb involvement
+BMGC_DS14830,BMG_DS056055,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10"
+BMGC_DS14831,BMG_DS056056,"SPINAL MUSCULAR ATROPHY, JOKELA TYPE"
+BMGC_DS14832,BMG_DS056057,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F"
+BMGC_DS14833,BMG_DS056058,HYPOTRICHOSIS 11
+BMGC_DS14834,BMG_DS056059,Distal arthrogryposis type 5D
+BMGC_DS14835,BMG_DS056060,"OSTEOGENESIS IMPERFECTA, TYPE XIV"
+BMGC_DS14836,BMG_DS056061,Microcephalic primordial dwarfism Alazami type
+BMGC_DS14837,BMG_DS056062,"BRACHYDACTYLY, TYPE A1, C"
+BMGC_DS14838,BMG_DS056063,GAND SYNDROME
+BMGC_DS14839,BMG_DS056064,NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS
+BMGC_DS14840,BMG_DS056065,ALZHEIMER DISEASE 17
+BMGC_DS14841,BMG_DS056066,SPERMATOGENIC FAILURE 11
+BMGC_DS14842,BMG_DS056067,"colorectal cancer, susceptibility to, 12"
+BMGC_DS14843,BMG_DS056068,MITOCHONDRIAL DNA DEPLETION SYNDROME 11
+BMGC_DS14844,BMG_DS056069,"OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8"
+BMGC_DS14845,BMG_DS056070,"autism, susceptibility to, 19"
+BMGC_DS14846,BMG_DS056071,LEFT VENTRICULAR NONCOMPACTION 7
+BMGC_DS14847,BMG_DS056072,"MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS14848,BMG_DS056073,COWDEN SYNDROME 4
+BMGC_DS14849,BMG_DS056074,COWDEN SYNDROME 5
+BMGC_DS14850,BMG_DS056075,COWDEN SYNDROME 6
+BMGC_DS14851,BMG_DS056076,UROFACIAL SYNDROME 2
+BMGC_DS14852,BMG_DS056077,"MICROPHTHALMIA, ISOLATED 8"
+BMGC_DS14853,BMG_DS056078,"CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2"
+BMGC_DS14854,BMG_DS056079,LYMPHOPROLIFERATIVE SYNDROME 2
+BMGC_DS14855,BMG_DS056080,"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 4"
+BMGC_DS14856,BMG_DS056082,"melanoma, cutaneous malignant, susceptibility to, 9"
+BMGC_DS14857,BMG_DS056083,"MAPLE SYRUP URINE DISEASE, MILD VARIANT"
+BMGC_DS14858,BMG_DS056084,"FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE"
+BMGC_DS14859,BMG_DS056086,MICROPHTHALMIA/COLOBOMA 9
+BMGC_DS14860,BMG_DS056087,"RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME"
+BMGC_DS14861,BMG_DS056088,Steel syndrome
+BMGC_DS14862,BMG_DS056089,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 6"
+BMGC_DS14863,BMG_DS056091,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2"
+BMGC_DS14864,BMG_DS056092,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3"
+BMGC_DS14865,BMG_DS056093,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4"
+BMGC_DS14866,BMG_DS056094,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5"
+BMGC_DS14867,BMG_DS056095,short ulna-dysmorphism-hypotonia-intellectual disability syndrome
+BMGC_DS14868,BMG_DS056096,CONE-ROD DYSTROPHY 17
+BMGC_DS14869,BMG_DS056097,"Syndactyly, camptodactyly and clinodactyly of fifth fingers, bifid toes syndrome"
+BMGC_DS14870,BMG_DS056098,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11"
+BMGC_DS14871,BMG_DS056099,"CARDIOMYOPATHY, DILATED, 1II"
+BMGC_DS14872,BMG_DS056100,"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5"
+BMGC_DS14873,BMG_DS056101,LISSENCEPHALY 5
+BMGC_DS14874,BMG_DS056102,"BLEEDING DISORDER, PLATELET-TYPE, 15"
+BMGC_DS14875,BMG_DS056104,Osteosclerotic metaphyseal dysplasia
+BMGC_DS14876,BMG_DS056105,IMMUNODEFICIENCY 11
+BMGC_DS14877,BMG_DS056106,IMMUNODEFICIENCY 56
+BMGC_DS14878,BMG_DS056107,"AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE"
+BMGC_DS14879,BMG_DS056108,ATAXIA-OCULOMOTOR APRAXIA 3
+BMGC_DS14880,BMG_DS056109,"HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES"
+BMGC_DS14881,BMG_DS056111,"Facial dysmorphism, conductive hearing loss, heart defect syndrome"
+BMGC_DS14882,BMG_DS056113,complete atrioventricular canal-tetralogy of fallot syndrome
+BMGC_DS14883,BMG_DS056116,posteroinferior myocardial infarction
+BMGC_DS14884,BMG_DS056117,apical myocardial infarction
+BMGC_DS14885,BMG_DS056119,endometrioid stromal sarcoma of the cervix
+BMGC_DS14886,BMG_DS056120,endometrioid stromal sarcoma of the vagina
+BMGC_DS14887,BMG_DS056122,luminal A breast carcinoma
+BMGC_DS14888,BMG_DS056123,luminal B breast carcinoma
+BMGC_DS14889,BMG_DS056125,posterolateral myocardial infarction
+BMGC_DS14890,BMG_DS056127,subendocardial myocardial infarction
+BMGC_DS14891,BMG_DS056128,Autosomal Recessive Centronuclear Myopathy
+BMGC_DS14892,BMG_DS056129,Congenital Osteopetrosis
+BMGC_DS14893,BMG_DS056153,Drug-Induced Acute Liver Injury
+BMGC_DS14894,BMG_DS056154,Hereditary Antithrombin Deficiency
+BMGC_DS14895,BMG_DS056155,Zellweger Spectrum
+BMGC_DS14896,BMG_DS056156,Mycoplasma-Induced Stevens-Johnson Syndrome
+BMGC_DS14897,BMG_DS056157,Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum
+BMGC_DS14898,BMG_DS056164,Partial Fetal Alcohol Syndrome
+BMGC_DS14899,BMG_DS056165,Autosomal Dominant Myotubular Myopathy
+BMGC_DS14900,BMG_DS056166,Hereditary Motor Neuronopathy
+BMGC_DS14901,BMG_DS056167,Congenital Intestinal Aganglionosis
+BMGC_DS14902,BMG_DS056168,Autosomal Recessive Chronic Granulomatous Disease
+BMGC_DS14903,BMG_DS056207,Perioperative hypertension
+BMGC_DS14904,BMG_DS056210,Dyslipidemia due to type 2 diabetes mellitus
+BMGC_DS14905,BMG_DS056232,Peroneal Nerve Entrapment
+BMGC_DS14906,BMG_DS056240,Radial Nerve Entrapment
+BMGC_DS14907,BMG_DS056250,Chronic kidney disease due to type 2 diabetes mellitus
+BMGC_DS14908,BMG_DS056286,Dextran pseudoallergy
+BMGC_DS14909,BMG_DS056363,Primary hypertrophic cardiomyopathy
+BMGC_DS14910,BMG_DS056364,Keratitis-Ichthyosis-Deafness Syndrome
+BMGC_DS14911,BMG_DS056367,Progressive Cone Dystrophy
+BMGC_DS14912,BMG_DS056368,Secondary hypothyroidism
+BMGC_DS14913,BMG_DS056369,Galactorrhea
+BMGC_DS14914,BMG_DS056370,"Arteriosclerotic cardiovascular disease, NOS"
+BMGC_DS14915,BMG_DS056372,"2,8-Dihydroxyadenine Urolithiasis"
+BMGC_DS14916,BMG_DS056375,Hemoglobin M Disease
+BMGC_DS14917,BMG_DS056382,Familial Osteochondritis Dissecans
+BMGC_DS14918,BMG_DS056387,Warts
+BMGC_DS14919,BMG_DS056391,uveal cancer
+BMGC_DS14920,BMG_DS056392,Chronic familial neutropenia (disorder)
+BMGC_DS14921,BMG_DS056393,Congenital reticular ichthyosiform erythroderma
+BMGC_DS14922,BMG_DS056401,"Luteinizing Hormone Resistance, Female"
+BMGC_DS14923,BMG_DS056402,Dmd-Associated Dilated Cardiomyopathy
+BMGC_DS14924,BMG_DS056403,atelosteogenesis type III
+BMGC_DS14925,BMG_DS056404,Fatty Acid Hydroxylase-Associated Neurodegeneration
+BMGC_DS14926,BMG_DS056406,11-Beta-hydroxylase deficiency
+BMGC_DS14927,BMG_DS056407,5-Alpha Reductase Deficiency
+BMGC_DS14928,BMG_DS056411,X-Linked Chondrodysplasia Punctata 1
+BMGC_DS14929,BMG_DS056421,Cyclic Hematopoesis
+BMGC_DS14930,BMG_DS056424,Autosomal Recessive Cerebellar Ataxia Type 1
+BMGC_DS14931,BMG_DS056429,dermatofibrosarcoma protuberans
+BMGC_DS14932,BMG_DS056431,Middle East Respiratory Syndrome
+BMGC_DS14933,BMG_DS056432,GLYCOGEN STORAGE DISEASE IXa1
+BMGC_DS14934,BMG_DS056436,Charcot-Marie-Tooth disease type 4B3
+BMGC_DS14935,BMG_DS056440,3-Methylglutaconic Aciduria
+BMGC_DS14936,BMG_DS056480,Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
+BMGC_DS14937,BMG_DS056495,Ulcerative colitis in remission
+BMGC_DS14938,BMG_DS056499,Acute exacerbation of chronic congestive heart failure
+BMGC_DS14939,BMG_DS056505,Pulmonary arterial hypertension associated with congenital heart disease
+BMGC_DS14940,BMG_DS056557,Non-specific intraventricular conduction delay
+BMGC_DS14941,BMG_DS056670,Anti-D isoimmunization affecting pregnancy
+BMGC_DS14942,BMG_DS056671,Pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis
+BMGC_DS14943,BMG_DS056708,porencephaly
+BMGC_DS14944,BMG_DS056715,"Ohdo syndrome, Maat-Kievit-Brunner type"
+BMGC_DS14945,BMG_DS056721,Cap Myopathy
+BMGC_DS14946,BMG_DS056723,Mitochondrial DNA Depletion Syndrome 8A
+BMGC_DS14947,BMG_DS056725,Metatropic Dysplasia Type 1
+BMGC_DS14948,BMG_DS056726,Surfactant Dysfunction
+BMGC_DS14949,BMG_DS056727,Succinate-Coa Ligase Deficiency
+BMGC_DS14950,BMG_DS056728,Spastic Paraplegia Type 7
+BMGC_DS14951,BMG_DS056730,Nonsyndromic Deafness
+BMGC_DS14952,BMG_DS056731,Isodicentric Chromosome 15 Syndrome
+BMGC_DS14953,BMG_DS056732,Intranuclear Rod Myopathy
+BMGC_DS14954,BMG_DS056734,Huntington Disease-Like Syndrome
+BMGC_DS14955,BMG_DS056735,Hereditary Diffuse Leukoencephalopathy with Spheroids
+BMGC_DS14956,BMG_DS056737,"Distal Hereditary Motor Neuropathy, Type II"
+BMGC_DS14957,BMG_DS056738,Deoxyguanosine Kinase Deficiency
+BMGC_DS14958,BMG_DS056740,Autosomal Recessive Primary Microcephaly
+BMGC_DS14959,BMG_DS056742,Actin-Accumulation Myopathy
+BMGC_DS14960,BMG_DS056743,9q22.3 Microdeletion
+BMGC_DS14961,BMG_DS056745,"Hdl Deficiency, Type 2"
+BMGC_DS14962,BMG_DS056746,X-Linked Csnb
+BMGC_DS14963,BMG_DS056750,Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
+BMGC_DS14964,BMG_DS056754,Familial Hyperaldosteronism
+BMGC_DS14965,BMG_DS056755,Childhood Myocerebrohepatopathy Spectrum
+BMGC_DS14966,BMG_DS056757,"46,XY Disorder of Sex Development Due To LH Defects"
+BMGC_DS14967,BMG_DS056758,Trisomy Xq28
+BMGC_DS14968,BMG_DS056759,"Blepharophimosis, Ptosis, and Epicanthus Inversus Type II"
+BMGC_DS14969,BMG_DS056760,"Trifunctional Protein Deficiency, Type 2"
+BMGC_DS14970,BMG_DS056761,Bmpr1a-Related Juvenile Polyposis
+BMGC_DS14971,BMG_DS056762,Smad4-Related Juvenile Polyposis
+BMGC_DS14972,BMG_DS056772,Meckel syndrome type 1
+BMGC_DS14973,BMG_DS056773,Nutrition Disorders
+BMGC_DS14974,BMG_DS056776,myxofibrosarcoma
+BMGC_DS14975,BMG_DS056777,Dowling-Degos disease
+BMGC_DS14976,BMG_DS056779,"hypokalemic periodic paralysis, type 1"
+BMGC_DS14977,BMG_DS056780,Multicystic Dysplastic Kidney
+BMGC_DS14978,BMG_DS056783,Primary Hyperthyroidism
+BMGC_DS14979,BMG_DS056786,Pneumonitis
+BMGC_DS14980,BMG_DS056787,thymus neoplasm
+BMGC_DS14981,BMG_DS056791,mesothelial neoplasm
+BMGC_DS14982,BMG_DS056793,"RETINOSCHISIS 1, X-LINKED, JUVENILE"
+BMGC_DS14983,BMG_DS056794,intellectual disability
+BMGC_DS14984,BMG_DS056795,Juvenile rheumatoid arthritis
+BMGC_DS14985,BMG_DS056796,Juvenile psoriatic arthritis
+BMGC_DS14986,BMG_DS056797,Drug-induced tardive dyskinesia
+BMGC_DS14987,BMG_DS056799,"Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia"
+BMGC_DS14988,BMG_DS056800,"Axenfeld-Rieger Syndrome, Type 1"
+BMGC_DS14989,BMG_DS056801,SMITH-MCCORT DYSPLASIA 2
+BMGC_DS14990,BMG_DS056802,"SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE"
+BMGC_DS14991,BMG_DS056803,"SYMPHALANGISM, PROXIMAL, 1A"
+BMGC_DS14992,BMG_DS056804,"multiple system atrophy 1, susceptibility to"
+BMGC_DS14993,BMG_DS056805,MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY
+BMGC_DS14994,BMG_DS056806,"MYOPATHY, MYOFIBRILLAR, 3"
+BMGC_DS14995,BMG_DS056807,OTOFACIOCERVICAL SYNDROME 1
+BMGC_DS14996,BMG_DS056808,OTOFACIOCERVICAL SYNDROME 2
+BMGC_DS14997,BMG_DS056809,PACHYONYCHIA CONGENITA 3
+BMGC_DS14998,BMG_DS056810,PACHYONYCHIA CONGENITA 4
+BMGC_DS14999,BMG_DS056811,"pulmonary hypertension, neonatal, susceptibility to"
+BMGC_DS15000,BMG_DS056812,ACTIVATED PI3K-DELTA SYNDROME
+BMGC_DS15001,BMG_DS056813,BARDET-BIEDL SYNDROME 17
+BMGC_DS15002,BMG_DS056814,"CANDIDIASIS, FAMILIAL, 8"
+BMGC_DS15003,BMG_DS056815,"CARDIOMYOPATHY, DILATED, 1KK"
+BMGC_DS15004,BMG_DS056816,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 22"
+BMGC_DS15005,BMG_DS056817,"CEROID LIPOFUSCINOSIS, NEURONAL, 13 (KUFS TYPE)"
+BMGC_DS15006,BMG_DS056818,CRANIOSYNOSTOSIS 3
+BMGC_DS15007,BMG_DS056819,DEVELOPMENTAL DYSPLASIA OF THE HIP 2
+BMGC_DS15008,BMG_DS056820,"EPIDERMOLYSIS BULLOSA SIMPLEX 1D, GENERALIZED, INTERMEDIATE OR SEVERE, AUTOSOMAL RECESSIVE"
+BMGC_DS15009,BMG_DS056821,"HYPOCALCEMIA, AUTOSOMAL DOMINANT 1"
+BMGC_DS15010,BMG_DS056823,AMYOTROPHIC LATERAL SCLEROSIS 19
+BMGC_DS15011,BMG_DS056824,AMYOTROPHIC LATERAL SCLEROSIS 20
+BMGC_DS15012,BMG_DS056825,LEBER CONGENITAL AMAUROSIS 17
+BMGC_DS15013,BMG_DS056826,LEFT VENTRICULAR NONCOMPACTION 10
+BMGC_DS15014,BMG_DS056827,mandibular hypoplasia-deafness-progeroid syndrome
+BMGC_DS15015,BMG_DS056828,RENAL-HEPATIC-PANCREATIC DYSPLASIA 1
+BMGC_DS15016,BMG_DS056829,RETINITIS PIGMENTOSA 66
+BMGC_DS15017,BMG_DS056836,CATARACT 13 WITH ADULT i PHENOTYPE
+BMGC_DS15018,BMG_DS056837,"ALBINISM, OCULOCUTANEOUS, TYPE VI"
+BMGC_DS15019,BMG_DS056838,CATARACT 29
+BMGC_DS15020,BMG_DS056839,"CATARACT 20, MULTIPLE TYPES"
+BMGC_DS15021,BMG_DS056840,CATARACT 30
+BMGC_DS15022,BMG_DS056841,CATARACT 41
+BMGC_DS15023,BMG_DS056842,"COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR IMPAIRED INTELLECTUAL DEVELOPMENT"
+BMGC_DS15024,BMG_DS056843,FOVEAL HYPOPLASIA 1
+BMGC_DS15025,BMG_DS056844,"CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED"
+BMGC_DS15026,BMG_DS056851,"MEGALENCEPHALY, AUTOSOMAL DOMINANT"
+BMGC_DS15027,BMG_DS056854,"PRECOCIOUS PUBERTY, CENTRAL, 1"
+BMGC_DS15028,BMG_DS056858,"ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1"
+BMGC_DS15029,BMG_DS056859,BARDET-BIEDL SYNDROME 18
+BMGC_DS15030,BMG_DS056863,"CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND IMPAIRED INTELLECTUAL DEVELOPMENT"
+BMGC_DS15031,BMG_DS056865,DEAFNESS AND MYOPIA
+BMGC_DS15032,BMG_DS056872,"MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE"
+BMGC_DS15033,BMG_DS056874,"XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME"
+BMGC_DS15034,BMG_DS056875,"CONGENITAL SHORT BOWEL SYNDROME, X-LINKED"
+BMGC_DS15035,BMG_DS056876,"DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION"
+BMGC_DS15036,BMG_DS056878,PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1
+BMGC_DS15037,BMG_DS056879,Solute carrier family 35 member A2 congenital disorder of glycosylation
+BMGC_DS15038,BMG_DS056880,"CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6"
+BMGC_DS15039,BMG_DS056882,susceptibility to angioedema induced by ACE inhibitors
+BMGC_DS15040,BMG_DS056883,"PARKINSONISM WITH SPASTICITY, X-LINKED"
+BMGC_DS15041,BMG_DS056884,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 98"
+BMGC_DS15042,BMG_DS056885,"DEAFNESS, X-LINKED 6"
+BMGC_DS15043,BMG_DS056886,"MICROPHTHALMIA, SYNDROMIC 13"
+BMGC_DS15044,BMG_DS056887,"OLMSTED SYNDROME, X-LINKED"
+BMGC_DS15045,BMG_DS056888,"intellectual disability, X-linked 99"
+BMGC_DS15046,BMG_DS056889,"GROWTH RETARDATION, PRENATAL, WITH PROGRESSIVE PANCYTOPENIA AND CEREBELLAR HYPOPLASIA"
+BMGC_DS15047,BMG_DS056891,CRANIOSYNOSTOSIS 4
+BMGC_DS15048,BMG_DS056892,"DYSERYTHROPOIESIS, CONGENITAL, WITH ULTRASTRUCTURALLY NORMAL ERYTHROBLAST HETEROCHROMATIN"
+BMGC_DS15049,BMG_DS056893,"CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT"
+BMGC_DS15050,BMG_DS056896,"ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1"
+BMGC_DS15051,BMG_DS056898,AMYOTROPHIC LATERAL SCLEROSIS 21
+BMGC_DS15052,BMG_DS056899,MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY
+BMGC_DS15053,BMG_DS056900,"LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 7"
+BMGC_DS15054,BMG_DS056904,CHROMOSOME 15q11.2 DUPLICATION SYNDROME
+BMGC_DS15055,BMG_DS056905,FOVEAL HYPOPLASIA 2
+BMGC_DS15056,BMG_DS056907,"CATARACT 23, MULTIPLE TYPES"
+BMGC_DS15057,BMG_DS056908,CATARACT 11 WITH MICROPHTHALMIA AND NEURODEVELOPMENTAL ABNORMALITIES
+BMGC_DS15058,BMG_DS056910,"CATARACT 33, MULTIPLE TYPES"
+BMGC_DS15059,BMG_DS056911,"CATARACT 12, MULTIPLE TYPES"
+BMGC_DS15060,BMG_DS056912,LEFT VENTRICULAR NONCOMPACTION 9
+BMGC_DS15061,BMG_DS056913,MICROTIA WITH OR WITHOUT HEARING IMPAIRMENT
+BMGC_DS15062,BMG_DS056915,"CHROMOSOME 17p13.3, CENTROMERIC, DUPLICATION SYNDROME"
+BMGC_DS15063,BMG_DS056916,"CATARACT 16, MULTIPLE TYPES"
+BMGC_DS15064,BMG_DS056917,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1"
+BMGC_DS15065,BMG_DS056918,PERRAULT SYNDROME 3
+BMGC_DS15066,BMG_DS056919,CHROMOSOME 2p16.3 DELETION SYNDROME
+BMGC_DS15067,BMG_DS056920,BONE MARROW FAILURE SYNDROME 1
+BMGC_DS15068,BMG_DS056921,IMMUNODEFICIENCY 32A
+BMGC_DS15069,BMG_DS056923,"EPISODIC PAIN SYNDROME, FAMILIAL, 1"
+BMGC_DS15070,BMG_DS056926,"MYASTHENIC SYNDROME, CONGENITAL, 8"
+BMGC_DS15071,BMG_DS056928,"ALBINISM, OCULOCUTANEOUS, TYPE VII"
+BMGC_DS15072,BMG_DS056929,"CATARACT 39, MULTIPLE TYPES"
+BMGC_DS15073,BMG_DS056930,"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 4"
+BMGC_DS15074,BMG_DS056931,"OSTEOGENESIS IMPERFECTA, TYPE XV"
+BMGC_DS15075,BMG_DS056932,"ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2"
+BMGC_DS15076,BMG_DS056933,corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome
+BMGC_DS15077,BMG_DS056934,"POLYDACTYLY, POSTAXIAL, TYPE A6"
+BMGC_DS15078,BMG_DS056935,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4B"
+BMGC_DS15079,BMG_DS056936,schizophrenia 18
+BMGC_DS15080,BMG_DS056937,"ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2"
+BMGC_DS15081,BMG_DS056939,"CARDIOMYOPATHY, DILATED, 1JJ"
+BMGC_DS15082,BMG_DS056940,CIDEC-related familial partial lipodystrophy
+BMGC_DS15083,BMG_DS056941,"NEPHROTIC SYNDROME, TYPE 8"
+BMGC_DS15084,BMG_DS056942,"CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 4"
+BMGC_DS15085,BMG_DS056943,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12"
+BMGC_DS15086,BMG_DS056944,HYPOGONADOTROPIC HYPOGONADISM 17 WITH OR WITHOUT ANOSMIA
+BMGC_DS15087,BMG_DS056945,HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA
+BMGC_DS15088,BMG_DS056946,"CEREBELLAR ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSEQUILIBRIUM SYNDROME 4"
+BMGC_DS15089,BMG_DS056947,HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA
+BMGC_DS15090,BMG_DS056948,HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA
+BMGC_DS15091,BMG_DS056949,HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA
+BMGC_DS15092,BMG_DS056950,"FANCONI ANEMIA, COMPLEMENTATION GROUP Q"
+BMGC_DS15093,BMG_DS056951,NGLY1 deficiency
+BMGC_DS15094,BMG_DS056952,"CATARACT 15, MULTIPLE TYPES"
+BMGC_DS15095,BMG_DS056953,"CATARACT 19, MULTIPLE TYPES"
+BMGC_DS15096,BMG_DS056954,CARDIOFACIOCUTANEOUS SYNDROME 2
+BMGC_DS15097,BMG_DS056955,CARDIOFACIOCUTANEOUS SYNDROME 3
+BMGC_DS15098,BMG_DS056956,CARDIOFACIOCUTANEOUS SYNDROME 4
+BMGC_DS15099,BMG_DS056957,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2"
+BMGC_DS15100,BMG_DS056958,"NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE"
+BMGC_DS15101,BMG_DS056960,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13"
+BMGC_DS15102,BMG_DS056961,"MYOFIBROMATOSIS, INFANTILE, 2"
+BMGC_DS15103,BMG_DS056962,"CILIARY DYSKINESIA, PRIMARY, 21"
+BMGC_DS15104,BMG_DS056963,ADAMS-OLIVER SYNDROME 4
+BMGC_DS15105,BMG_DS056967,"SYMPHALANGISM, PROXIMAL, 1B"
+BMGC_DS15106,BMG_DS056968,PERRAULT SYNDROME 4
+BMGC_DS15107,BMG_DS056969,DOWLING-DEGOS DISEASE 2
+BMGC_DS15108,BMG_DS056970,"Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome"
+BMGC_DS15109,BMG_DS056971,Multiple mitochondrial dysfunctions syndrome type 3
+BMGC_DS15110,BMG_DS056972,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 16
+BMGC_DS15111,BMG_DS056974,"PULMONARY HYPERTENSION, PRIMARY, 3"
+BMGC_DS15112,BMG_DS056975,"PULMONARY HYPERTENSION, PRIMARY, 4"
+BMGC_DS15113,BMG_DS056976,Central precocious puberty 2
+BMGC_DS15114,BMG_DS056977,NEMALINE MYOPATHY 8
+BMGC_DS15115,BMG_DS056978,B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome
+BMGC_DS15116,BMG_DS056979,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14"
+BMGC_DS15117,BMG_DS056980,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 14"
+BMGC_DS15118,BMG_DS056981,NOONAN SYNDROME 8
+BMGC_DS15119,BMG_DS056982,"HYPOCALCEMIA, AUTOSOMAL DOMINANT 2"
+BMGC_DS15120,BMG_DS056983,ESTROGEN RESISTANCE
+BMGC_DS15121,BMG_DS056987,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94
+BMGC_DS15122,BMG_DS056988,LEFT VENTRICULAR NONCOMPACTION 8
+BMGC_DS15123,BMG_DS056989,"CARDIOMYOPATHY, DILATED, 1LL"
+BMGC_DS15124,BMG_DS056990,CONE-ROD DYSTROPHY 18
+BMGC_DS15125,BMG_DS056991,"CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C"
+BMGC_DS15126,BMG_DS056992,"ATRIAL FIBRILLATION, FAMILIAL, 13"
+BMGC_DS15127,BMG_DS056993,"ATRIAL FIBRILLATION, FAMILIAL, 14"
+BMGC_DS15128,BMG_DS056994,NEPHRONOPHTHISIS 16
+BMGC_DS15129,BMG_DS056995,IMMUNODEFICIENCY 7
+BMGC_DS15130,BMG_DS056997,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 16
+BMGC_DS15131,BMG_DS056998,"CARDIOMYOPATHY, DILATED, 1MM"
+BMGC_DS15132,BMG_DS057001,"MECKEL SYNDROME, TYPE 11"
+BMGC_DS15133,BMG_DS057002,MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3
+BMGC_DS15134,BMG_DS057003,PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2
+BMGC_DS15135,BMG_DS057004,"EPILEPSY, EARLY-ONSET, 5, WITH OR WITHOUT DEVELOPMENTAL DELAY"
+BMGC_DS15136,BMG_DS057005,Severe combined immunodeficiency due to CORO1A deficiency
+BMGC_DS15137,BMG_DS057006,DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3
+BMGC_DS15138,BMG_DS057007,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3"
+BMGC_DS15139,BMG_DS057008,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4"
+BMGC_DS15140,BMG_DS057009,SPERMATOGENIC FAILURE 12
+BMGC_DS15141,BMG_DS057010,"MICROCEPHALY 11, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS15142,BMG_DS057011,RENAL-HEPATIC-PANCREATIC DYSPLASIA 2
+BMGC_DS15143,BMG_DS057012,"MITOCHONDRIAL DNA DEPLETION SYNDROME 12B (CARDIOMYOPATHIC TYPE), AUTOSOMAL RECESSIVE"
+BMGC_DS15144,BMG_DS057013,"HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1"
+BMGC_DS15145,BMG_DS057014,"MYOPIA 22, AUTOSOMAL DOMINANT"
+BMGC_DS15146,BMG_DS057015,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
+BMGC_DS15148,BMG_DS057017,"EPIDERMOLYSIS BULLOSA SIMPLEX 3, LOCALIZED OR GENERALIZED INTERMEDIATE, WITH BP230 DEFICIENCY"
+BMGC_DS15149,BMG_DS057018,"MYOPIA 23, AUTOSOMAL RECESSIVE"
+BMGC_DS15150,BMG_DS057019,SPECIFIC LANGUAGE IMPAIRMENT 5
+BMGC_DS15151,BMG_DS057020,CHROMOSOME 3q13.31 DELETION SYNDROME
+BMGC_DS15152,BMG_DS057021,"AORTIC ANEURYSM, FAMILIAL THORACIC 8"
+BMGC_DS15153,BMG_DS057022,INFANTILE LIVER FAILURE SYNDROME 1
+BMGC_DS15154,BMG_DS057023,"MACULAR DEGENERATION, AGE-RELATED, 13"
+BMGC_DS15155,BMG_DS057024,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17
+BMGC_DS15156,BMG_DS057025,"CARDIAC ARRHYTHMIA SYNDROME, WITH OR WITHOUT SKELETAL MUSCLE WEAKNESS"
+BMGC_DS15157,BMG_DS057026,"CILIARY DYSKINESIA, PRIMARY, 22"
+BMGC_DS15158,BMG_DS057027,"CILIARY DYSKINESIA, PRIMARY, 23"
+BMGC_DS15159,BMG_DS057028,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6"
+BMGC_DS15160,BMG_DS057030,"MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS"
+BMGC_DS15161,BMG_DS057031,IMMUNODEFICIENCY 12
+BMGC_DS15162,BMG_DS057032,FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome
+BMGC_DS15163,BMG_DS057033,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17"
+BMGC_DS15164,BMG_DS057034,"PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES"
+BMGC_DS15165,BMG_DS057036,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 18
+BMGC_DS15166,BMG_DS057037,"CILIARY DYSKINESIA, PRIMARY, 24"
+BMGC_DS15167,BMG_DS057038,"CILIARY DYSKINESIA, PRIMARY, 25"
+BMGC_DS15168,BMG_DS057039,"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5"
+BMGC_DS15169,BMG_DS057040,INFANTILE LIVER FAILURE SYNDROME 2
+BMGC_DS15170,BMG_DS057041,"MACULAR DEGENERATION, AGE-RELATED, 14"
+BMGC_DS15171,BMG_DS057042,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R"
+BMGC_DS15172,BMG_DS057043,"SPASTIC PARAPLEGIA 79B, AUTOSOMAL RECESSIVE"
+BMGC_DS15173,BMG_DS057044,intellectual disability-hypotonia-spasticity-sleep disorder syndrome
+BMGC_DS15174,BMG_DS057045,"CILIARY DYSKINESIA, PRIMARY, 26"
+BMGC_DS15175,BMG_DS057046,intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome
+BMGC_DS15176,BMG_DS057047,SHORT-RIB THORACIC DYSPLASIA 8 WITH OR WITHOUT POLYDACTYLY
+BMGC_DS15177,BMG_DS057048,"CILIARY DYSKINESIA, PRIMARY, 27"
+BMGC_DS15178,BMG_DS057049,"CILIARY DYSKINESIA, PRIMARY, 28"
+BMGC_DS15179,BMG_DS057050,"TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5"
+BMGC_DS15180,BMG_DS057051,"Severe dermatitis, multiple allergies, metabolic wasting syndrome"
+BMGC_DS15181,BMG_DS057054,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 38"
+BMGC_DS15182,BMG_DS057055,IMMUNODEFICIENCY 13
+BMGC_DS15183,BMG_DS057057,Cole disease
+BMGC_DS15184,BMG_DS057063,"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 8"
+BMGC_DS15185,BMG_DS057064,"MICROPHTHALMIA, SYNDROMIC 12"
+BMGC_DS15186,BMG_DS057065,"PARKINSON DISEASE 19A, JUVENILE-ONSET"
+BMGC_DS15187,BMG_DS057066,"craniosynostosis 5, susceptibility to"
+BMGC_DS15188,BMG_DS057067,"PARKINSON DISEASE 20, EARLY-ONSET"
+BMGC_DS15189,BMG_DS057069,CHROMOSOME 22q13 DUPLICATION SYNDROME
+BMGC_DS15190,BMG_DS057070,"EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2"
+BMGC_DS15191,BMG_DS057071,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 39"
+BMGC_DS15192,BMG_DS057072,TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE
+BMGC_DS15193,BMG_DS057074,PERIVENTRICULAR NODULAR HETEROTOPIA 6
+BMGC_DS15194,BMG_DS057075,"leukemia, acute lymphoblastic, susceptibility to, 3"
+BMGC_DS15195,BMG_DS057076,VAN MALDERGEM SYNDROME 2
+BMGC_DS15196,BMG_DS057077,Prader-Willi-like syndrome
+BMGC_DS15197,BMG_DS057078,Hereditary sensory and autonomic neuropathy type 7
+BMGC_DS15198,BMG_DS057079,DIAMOND-BLACKFAN ANEMIA 12
+BMGC_DS15199,BMG_DS057080,"EPISODIC PAIN SYNDROME, FAMILIAL, 2"
+BMGC_DS15200,BMG_DS057081,"EPISODIC PAIN SYNDROME, FAMILIAL, 3"
+BMGC_DS15201,BMG_DS057082,"ARTHROGRYPOSIS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES"
+BMGC_DS15202,BMG_DS057083,multiple fibroadenoma of the breast
+BMGC_DS15203,BMG_DS057084,"melioidosis, susceptibility to"
+BMGC_DS15204,BMG_DS057085,"AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III"
+BMGC_DS15205,BMG_DS057086,COMPLEMENT FACTOR B DEFICIENCY
+BMGC_DS15206,BMG_DS057087,RETINITIS PIGMENTOSA 67
+BMGC_DS15207,BMG_DS057088,"NEPHROTIC SYNDROME, TYPE 9"
+BMGC_DS15208,BMG_DS057089,"Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome (disorder)"
+BMGC_DS15209,BMG_DS057090,"IMMUNODEFICIENCY, COMMON VARIABLE, 10"
+BMGC_DS15210,BMG_DS057091,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18
+BMGC_DS15211,BMG_DS057092,RIENHOFF SYNDROME
+BMGC_DS15212,BMG_DS057093,8q24.3 microdeletion syndrome
+BMGC_DS15213,BMG_DS057094,ALZHEIMER DISEASE 18
+BMGC_DS15214,BMG_DS057095,"MACULAR DEGENERATION, AGE-RELATED, 15"
+BMGC_DS15215,BMG_DS057096,IMMUNODEFICIENCY 16
+BMGC_DS15216,BMG_DS057097,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19
+BMGC_DS15217,BMG_DS057098,Congenital disorder of glycosylation type 1w
+BMGC_DS15218,BMG_DS057099,Palmoplantar keratoderma Nagashima type
+BMGC_DS15219,BMG_DS057100,"NEURODEVELOPMENTAL DISORDER WITH FEEDING DIFFICULTIES, THIN CORPUS CALLOSUM, AND FOOT DEFORMITY"
+BMGC_DS15220,BMG_DS057101,L-ferritin deficiency
+BMGC_DS15221,BMG_DS057103,FANCONI RENOTUBULAR SYNDROME 3
+BMGC_DS15222,BMG_DS057104,IMMUNODEFICIENCY 17
+BMGC_DS15223,BMG_DS057105,IMMUNODEFICIENCY 18
+BMGC_DS15224,BMG_DS057106,"IMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT"
+BMGC_DS15225,BMG_DS057107,"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13"
+BMGC_DS15226,BMG_DS057108,IMMUNODEFICIENCY 19
+BMGC_DS15227,BMG_DS057109,"cholangiocarcinoma, susceptibility to"
+BMGC_DS15228,BMG_DS057110,"DEAFNESS, AUTOSOMAL DOMINANT 56"
+BMGC_DS15229,BMG_DS057111,SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY
+BMGC_DS15230,BMG_DS057113,"ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib"
+BMGC_DS15231,BMG_DS057114,"NEUROPATHY, HEREDITARY SENSORY, TYPE IF"
+BMGC_DS15232,BMG_DS057115,SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY
+BMGC_DS15233,BMG_DS057116,JOUBERT SYNDROME 21
+BMGC_DS15234,BMG_DS057117,macrocephaly-developmental delay syndrome
+BMGC_DS15235,BMG_DS057118,WARBURG MICRO SYNDROME 4
+BMGC_DS15236,BMG_DS057119,JOUBERT SYNDROME 22
+BMGC_DS15237,BMG_DS057120,CHROMOSOME 5q12 DELETION SYNDROME
+BMGC_DS15238,BMG_DS057121,SCHWANNOMATOSIS 2
+BMGC_DS15239,BMG_DS057122,MYOPATHY WITH EXTRAPYRAMIDAL SIGNS
+BMGC_DS15240,BMG_DS057123,DOWLING-DEGOS DISEASE 3
+BMGC_DS15241,BMG_DS057124,"SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE"
+BMGC_DS15242,BMG_DS057125,"SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE"
+BMGC_DS15243,BMG_DS057126,"SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE"
+BMGC_DS15244,BMG_DS057127,DOWLING-DEGOS DISEASE 4
+BMGC_DS15245,BMG_DS057128,"EPILEPSY, FAMILIAL TEMPORAL LOBE, 6"
+BMGC_DS15246,BMG_DS057129,MORBID OBESITY AND SPERMATOGENIC FAILURE
+BMGC_DS15247,BMG_DS057130,"POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS"
+BMGC_DS15248,BMG_DS057131,"Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency (disorder)"
+BMGC_DS15249,BMG_DS057132,AURICULOCONDYLAR SYNDROME 3
+BMGC_DS15250,BMG_DS057133,IMMUNODEFICIENCY 20
+BMGC_DS15251,BMG_DS057134,SACRAL AGENESIS WITH VERTEBRAL ANOMALIES
+BMGC_DS15252,BMG_DS057135,ALZHEIMER DISEASE 19
+BMGC_DS15253,BMG_DS057136,BONE MARROW FAILURE SYNDROME 2
+BMGC_DS15254,BMG_DS057137,HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 4
+BMGC_DS15255,BMG_DS057138,RENAL HYPODYSPLASIA/APLASIA 2
+BMGC_DS15256,BMG_DS057139,"Optic atrophy, intellectual disability syndrome"
+BMGC_DS15257,BMG_DS057141,PREMATURE OVARIAN FAILURE 8
+BMGC_DS15258,BMG_DS057142,PREMATURE OVARIAN FAILURE 9
+BMGC_DS15259,BMG_DS057143,RETINITIS PIGMENTOSA 68
+BMGC_DS15260,BMG_DS057144,NEMALINE MYOPATHY 9
+BMGC_DS15261,BMG_DS057145,"PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL OR DIFFUSE"
+BMGC_DS15262,BMG_DS057146,"developmental and epileptic encephalopathy, 19"
+BMGC_DS15263,BMG_DS057147,ATRIAL STANDSTILL 2
+BMGC_DS15264,BMG_DS057148,"ECULIZUMAB, POOR RESPONSE TO"
+BMGC_DS15265,BMG_DS057149,MOYAMOYA DISEASE 6 WITH OR WITHOUT ACHALASIA
+BMGC_DS15266,BMG_DS057150,"CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO"
+BMGC_DS15267,BMG_DS057151,"POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE"
+BMGC_DS15268,BMG_DS057152,intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
+BMGC_DS15269,BMG_DS057153,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5"
+BMGC_DS15270,BMG_DS057154,Low frequency sensorineural hearing loss
+BMGC_DS15271,BMG_DS057168,Mycoplasma pneumoniae Infection
+BMGC_DS15272,BMG_DS057182,Acute bacterial otitis externa
+BMGC_DS15273,BMG_DS057187,"MECKEL SYNDROME, TYPE 8"
+BMGC_DS15274,BMG_DS057188,"HYPERTENSION, SALT-SENSITIVE ESSENTIAL, SUSCEPTIBILITY TO"
+BMGC_DS15275,BMG_DS057190,"Diabetes Mellitus, Ketosis-Prone"
+BMGC_DS15276,BMG_DS057191,"pulmonary disease, chronic obstructive, susceptibility to"
+BMGC_DS15277,BMG_DS057201,Familial hyperaldosteronism type 1
+BMGC_DS15278,BMG_DS057208,Familial hyperaldosteronism type 3
+BMGC_DS15279,BMG_DS057238,Bartter syndrome type 4
+BMGC_DS15280,BMG_DS057244,phakomatosis cesioflammea
+BMGC_DS15281,BMG_DS057317,Cerebrofacial arteriovenous metameric syndrome
+BMGC_DS15282,BMG_DS057323,phakomatosis cesiomarmorata
+BMGC_DS15283,BMG_DS057422,infiltrating nipple syringomatous adenoma
+BMGC_DS15284,BMG_DS057442,DICER1-related tumor predisposition
+BMGC_DS15285,BMG_DS057455,Familial cerebral saccular aneurysm
+BMGC_DS15286,BMG_DS057468,diffuse lymphatic malformation
+BMGC_DS15287,BMG_DS057553,rete ovarii adenocarcinoma
+BMGC_DS15288,BMG_DS057557,pseudomyogenic hemangioendothelioma
+BMGC_DS15289,BMG_DS057562,Beta plus thalassemia
+BMGC_DS15290,BMG_DS057566,Acute Mesenteric Arterial Embolus
+BMGC_DS15291,BMG_DS057567,Occlusive Mesenteric Arterial Ischemia
+BMGC_DS15292,BMG_DS057568,Nonocclusive Mesenteric Ischemia
+BMGC_DS15293,BMG_DS057569,Acute Mesenteric Arterial Thrombosis
+BMGC_DS15294,BMG_DS057571,Severe Congenital Microcephaly
+BMGC_DS15295,BMG_DS057578,Erosive Duodenitis
+BMGC_DS15296,BMG_DS057580,Neonatal Alloimmune Thrombocytopenia
+BMGC_DS15297,BMG_DS057584,Lipodystrophy due to Human immunodeficiency virus infection and antiretroviral therapy
+BMGC_DS15298,BMG_DS057586,linear nevus sebaceous syndrome
+BMGC_DS15299,BMG_DS057595,Morvan syndrome
+BMGC_DS15300,BMG_DS057597,Hyperferritinemia
+BMGC_DS15301,BMG_DS057607,fetal and neonatal alloimmune thrombocytopenia
+BMGC_DS15302,BMG_DS057716,Recurrent candidiasis of vagina
+BMGC_DS15303,BMG_DS057727,Pulmonary emphysema co-occurrent with fibrosis of lung
+BMGC_DS15304,BMG_DS057831,Dermatophagoides pteronyssinus Allergy
+BMGC_DS15305,BMG_DS057850,second branchial cleft anomaly
+BMGC_DS15306,BMG_DS057861,Therapeutic opioid induced constipation
+BMGC_DS15307,BMG_DS057873,Intestinal hemorrhage due to angiodysplasia of intestine
+BMGC_DS15308,BMG_DS057934,Familial hyperalphalipoproteinemia
+BMGC_DS15309,BMG_DS057996,Complex dyslipidemia
+BMGC_DS15310,BMG_DS058001,Inflammatory dermatosis
+BMGC_DS15311,BMG_DS058022,Dermatophagoides farinae Allergy
+BMGC_DS15312,BMG_DS058038,"Neutrophil Chemotactic Response, Abnormal"
+BMGC_DS15313,BMG_DS058041,"migraine with or without aura, susceptibility to, 1"
+BMGC_DS15314,BMG_DS058042,Postaxial polydactyly type A
+BMGC_DS15315,BMG_DS058045,"ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE"
+BMGC_DS15316,BMG_DS058047,"bifid nose, autosomal recessive"
+BMGC_DS15317,BMG_DS058048,Renal cyst
+BMGC_DS15318,BMG_DS058049,"lipodystrophy, partial, acquired, susceptibility to"
+BMGC_DS15319,BMG_DS058050,Hyperkinesia
+BMGC_DS15320,BMG_DS058052,Very long chain acyl-CoA dehydrogenase deficiency
+BMGC_DS15321,BMG_DS058053,"Keratosis Follicularis Spinulosa Decalvans, X-Linked"
+BMGC_DS15322,BMG_DS058054,osteoarthritis susceptibility 2
+BMGC_DS15323,BMG_DS058055,Keratoglobus
+BMGC_DS15324,BMG_DS058058,Hemophagocytic Syndrome
+BMGC_DS15325,BMG_DS058062,"HYDROCEPHALUS, CONGENITAL, 1"
+BMGC_DS15326,BMG_DS058063,"Dandy-Walker Syndrome, Familial"
+BMGC_DS15327,BMG_DS058065,Autoimmune gastritis
+BMGC_DS15328,BMG_DS058067,Job Syndrome
+BMGC_DS15329,BMG_DS058068,Adult Rickets
+BMGC_DS15330,BMG_DS058070,"POLYARTERITIS NODOSA, CHILDHOOD-ONSET"
+BMGC_DS15331,BMG_DS058071,"PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT"
+BMGC_DS15332,BMG_DS058074,Infection by larvae of Trichinella spiralis
+BMGC_DS15333,BMG_DS058079,optic nerve disorder
+BMGC_DS15334,BMG_DS058080,WILMS TUMOR 2
+BMGC_DS15335,BMG_DS058082,osteoarthritis susceptibility 1
+BMGC_DS15336,BMG_DS058085,Aortic Valve Disease 1
+BMGC_DS15337,BMG_DS058087,Enteritis due to Yersinia enterocolitica
+BMGC_DS15338,BMG_DS058091,"CATARACT 32, MULTIPLE TYPES"
+BMGC_DS15339,BMG_DS058092,"DEAFNESS, AUTOSOMAL DOMINANT 27"
+BMGC_DS15340,BMG_DS058093,"DEAFNESS, AUTOSOMAL DOMINANT 33"
+BMGC_DS15341,BMG_DS058094,"MYOCLONIC EPILEPSY, JUVENILE, 2"
+BMGC_DS15342,BMG_DS058095,"CONE DYSTROPHY 5, X-LINKED"
+BMGC_DS15343,BMG_DS058096,Deuteranomaly
+BMGC_DS15344,BMG_DS058097,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 41"
+BMGC_DS15345,BMG_DS058098,"GLAUCOMA 1, OPEN ANGLE, B"
+BMGC_DS15346,BMG_DS058100,POLYCYSTIC KIDNEY DISEASE 3 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE
+BMGC_DS15347,BMG_DS058101,"RETINAL DYSPLASIA, PRIMARY"
+BMGC_DS15348,BMG_DS058102,Protanomaly
+BMGC_DS15349,BMG_DS058104,RETINITIS PIGMENTOSA 24
+BMGC_DS15350,BMG_DS058105,SPINOCEREBELLAR ATAXIA 9
+BMGC_DS15351,BMG_DS058106,HERMANSKY-PUDLAK SYNDROME 3
+BMGC_DS15352,BMG_DS058107,"PULMONARY HYPERTENSION, PRIMARY, 2"
+BMGC_DS15353,BMG_DS058108,HERMANSKY-PUDLAK SYNDROME 5
+BMGC_DS15354,BMG_DS058109,HERMANSKY-PUDLAK SYNDROME 6
+BMGC_DS15355,BMG_DS058110,"MACULAR DYSTROPHY, RETINAL, 3"
+BMGC_DS15356,BMG_DS058112,Congenital Hyperinsulinism
+BMGC_DS15357,BMG_DS058113,Cacosmia
+BMGC_DS15358,BMG_DS058114,HERMANSKY-PUDLAK SYNDROME 8
+BMGC_DS15359,BMG_DS058116,"DEAFNESS, AUTOSOMAL DOMINANT 54"
+BMGC_DS15360,BMG_DS058117,"DEAFNESS, AUTOSOMAL RECESSIVE 45"
+BMGC_DS15361,BMG_DS058118,SPINOCEREBELLAR ATAXIA 35
+BMGC_DS15362,BMG_DS058120,"ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT"
+BMGC_DS15363,BMG_DS058121,"DEAFNESS, Y-LINKED 1"
+BMGC_DS15364,BMG_DS058122,"Charcot-Marie-Tooth disease, Type 2I"
+BMGC_DS15365,BMG_DS058123,SMITH-MCCORT DYSPLASIA 1
+BMGC_DS15366,BMG_DS058124,"Deafness, X-Linked 3"
+BMGC_DS15367,BMG_DS058125,Early onset torsion dystonia
+BMGC_DS15368,BMG_DS058126,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2"
+BMGC_DS15369,BMG_DS058128,Autosomal dominant vitreoretinochoroidopathy
+BMGC_DS15370,BMG_DS058129,Frontotemporal Dementia With Motor Neuron Disease
+BMGC_DS15371,BMG_DS058130,Glomerulopathy with fibronectin deposits
+BMGC_DS15372,BMG_DS058131,"multiple sclerosis, susceptibility to 1"
+BMGC_DS15373,BMG_DS058133,"DEAFNESS, AUTOSOMAL DOMINANT 50"
+BMGC_DS15374,BMG_DS058134,"CATARACT 17, MULTIPLE TYPES"
+BMGC_DS15375,BMG_DS058135,"BESTROPHINOPATHY, AUTOSOMAL RECESSIVE"
+BMGC_DS15376,BMG_DS058136,APOLIPOPROTEIN A-II DEFICIENCY
+BMGC_DS15377,BMG_DS058137,ACTN3 DEFICIENCY
+BMGC_DS15378,BMG_DS058138,"SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT"
+BMGC_DS15379,BMG_DS058139,"SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE"
+BMGC_DS15380,BMG_DS058140,"DEAFNESS, AUTOSOMAL DOMINANT 58"
+BMGC_DS15381,BMG_DS058141,"MYOPIA 17, AUTOSOMAL DOMINANT"
+BMGC_DS15382,BMG_DS058142,SECKEL SYNDROME 4
+BMGC_DS15383,BMG_DS058143,"Hirschsprung disease, susceptibility to, 1"
+BMGC_DS15384,BMG_DS058144,AICARDI-GOUTIERES SYNDROME 7
+BMGC_DS15385,BMG_DS058145,"neuronopathy, distal hereditary motor, type 2D"
+BMGC_DS15386,BMG_DS058146,"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT"
+BMGC_DS15387,BMG_DS058147,"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT"
+BMGC_DS15388,BMG_DS058148,"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT"
+BMGC_DS15389,BMG_DS058149,"DEAFNESS, AUTOSOMAL RECESSIVE 83"
+BMGC_DS15390,BMG_DS058151,"Myopathy, familial idiopathic inflammatory"
+BMGC_DS15391,BMG_DS058152,"DEAFNESS, AUTOSOMAL RECESSIVE 96"
+BMGC_DS15392,BMG_DS058153,"GLAUCOMA 1, OPEN ANGLE, P"
+BMGC_DS15393,BMG_DS058154,OTOSCLEROSIS 10
+BMGC_DS15394,BMG_DS058155,"DEAFNESS, AUTOSOMAL RECESSIVE 93"
+BMGC_DS15395,BMG_DS058156,peroxisome biogenesis disorder 7A (Zellweger)
+BMGC_DS15396,BMG_DS058158,oculocutaneous albinism type 5
+BMGC_DS15397,BMG_DS058159,"CATARACT 5, MULTIPLE TYPES"
+BMGC_DS15398,BMG_DS058160,autoimmune uveitis
+BMGC_DS15399,BMG_DS058161,monogenic diabetes
+BMGC_DS15400,BMG_DS058162,Hemorrhagic Necrotic Pancreatitis
+BMGC_DS15401,BMG_DS058163,Hyperosmolar Hyperglycemic State
+BMGC_DS15402,BMG_DS058166,"Glycogen storage disease due to acid maltase deficiency, infantile onset"
+BMGC_DS15403,BMG_DS058167,Cryptococcus gattii Infection
+BMGC_DS15404,BMG_DS058169,Non-Radiographic Axial Spondyloarthritis
+BMGC_DS15405,BMG_DS058170,BARDET-BIEDL SYNDROME 16
+BMGC_DS15406,BMG_DS058171,BARDET-BIEDL SYNDROME 19
+BMGC_DS15407,BMG_DS058172,SPINOCEREBELLAR ATAXIA 37
+BMGC_DS15408,BMG_DS058174,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 100"
+BMGC_DS15409,BMG_DS058175,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 101"
+BMGC_DS15410,BMG_DS058176,rheumatoid factor-negative juvenile idiopathic arthritis
+BMGC_DS15411,BMG_DS058178,NEPHRONOPHTHISIS 18
+BMGC_DS15412,BMG_DS058180,autoinflammatory syndrome
+BMGC_DS15413,BMG_DS058182,Wilms tumor 6
+BMGC_DS15414,BMG_DS058183,"neural tube defects, susceptibility to"
+BMGC_DS15415,BMG_DS058184,SECKEL SYNDROME 8
+BMGC_DS15416,BMG_DS058185,CHROMOSOME Xq26.3 DUPLICATION SYNDROME
+BMGC_DS15417,BMG_DS058187,"Arthritis, Suppurative"
+BMGC_DS15418,BMG_DS058188,PANCREATIC AGENESIS 1
+BMGC_DS15419,BMG_DS058189,BARDET-BIEDL SYNDROME 5
+BMGC_DS15420,BMG_DS058190,"DEAFNESS, AUTOSOMAL DOMINANT 65"
+BMGC_DS15421,BMG_DS058191,"DEAFNESS, AUTOSOMAL RECESSIVE 101"
+BMGC_DS15422,BMG_DS058192,"DEAFNESS, AUTOSOMAL RECESSIVE 102"
+BMGC_DS15423,BMG_DS058193,familial colorectal cancer type X
+BMGC_DS15424,BMG_DS058196,Smouldering systemic mastocytosis
+BMGC_DS15425,BMG_DS058205,DISABLING PANSCLEROTIC MORPHEA OF CHILDHOOD
+BMGC_DS15426,BMG_DS058215,CIC-rearranged sarcoma
+BMGC_DS15427,BMG_DS058219,short stature due to primary acid-labile subunit deficiency
+BMGC_DS15428,BMG_DS058220,"AMELOGENESIS IMPERFECTA, TYPE IA"
+BMGC_DS15429,BMG_DS058221,CATARACT 42
+BMGC_DS15430,BMG_DS058222,"MYOPATHY, DISTAL, INFANTILE-ONSET"
+BMGC_DS15431,BMG_DS058223,"MYOPATHY, TUBULAR AGGREGATE, 1"
+BMGC_DS15432,BMG_DS058224,Behavioral variant of frontotemporal dementia
+BMGC_DS15433,BMG_DS058225,WHITE SPONGE NEVUS 1
+BMGC_DS15434,BMG_DS058227,IMMUNODEFICIENCY 27A
+BMGC_DS15435,BMG_DS058228,"COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE"
+BMGC_DS15436,BMG_DS058230,HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 1
+BMGC_DS15437,BMG_DS058231,"NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID"
+BMGC_DS15438,BMG_DS058234,DESBUQUOIS DYSPLASIA 1
+BMGC_DS15439,BMG_DS058235,Neonatal pulmonary hypertension
+BMGC_DS15440,BMG_DS058238,"TETRAAMELIA SYNDROME, AUTOSOMAL RECESSIVE"
+BMGC_DS15441,BMG_DS058240,Congenital disorder of glycosylation type 1y
+BMGC_DS15442,BMG_DS058243,"pituitary adenoma, growth hormone-secreting, 2"
+BMGC_DS15443,BMG_DS058245,"ALACRIMA, CONGENITAL, AUTOSOMAL RECESSIVE"
+BMGC_DS15444,BMG_DS058246,MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 1
+BMGC_DS15445,BMG_DS058247,ataxia-telangiectasia-like disorder 1
+BMGC_DS15446,BMG_DS058255,"epilepsy, idiopathic generalized, susceptibility to, 13"
+BMGC_DS15447,BMG_DS058256,"atrial fibrillation, familial, 17"
+BMGC_DS15448,BMG_DS058258,Progressive pulmonary failure
+BMGC_DS15449,BMG_DS058261,"POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL"
+BMGC_DS15450,BMG_DS058262,"atrial fibrillation, familial, 16"
+BMGC_DS15451,BMG_DS058263,intellectual disability-severe speech delay-mild dysmorphism syndrome
+BMGC_DS15452,BMG_DS058265,IMMUNODEFICIENCY 28
+BMGC_DS15453,BMG_DS058266,IMMUNODEFICIENCY 29
+BMGC_DS15454,BMG_DS058267,IMMUNODEFICIENCY 30
+BMGC_DS15455,BMG_DS058268,IMMUNODEFICIENCY 31A
+BMGC_DS15456,BMG_DS058274,IMMUNODEFICIENCY 22
+BMGC_DS15457,BMG_DS058275,"MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY"
+BMGC_DS15458,BMG_DS058276,"ATRIAL FIBRILLATION, FAMILIAL, 15"
+BMGC_DS15459,BMG_DS058277,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6"
+BMGC_DS15460,BMG_DS058278,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 1
+BMGC_DS15461,BMG_DS058279,DESBUQUOIS DYSPLASIA 2
+BMGC_DS15462,BMG_DS058280,"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4"
+BMGC_DS15463,BMG_DS058281,RETINITIS PIGMENTOSA 69
+BMGC_DS15464,BMG_DS058283,WHITE SPONGE NEVUS 2
+BMGC_DS15465,BMG_DS058284,"ROTHMUND-THOMSON SYNDROME, TYPE 3"
+BMGC_DS15466,BMG_DS058285,"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FEATURES, SPASTICITY, AND BRAIN ABNORMALITIES"
+BMGC_DS15467,BMG_DS058286,"PONTOCEREBELLAR HYPOPLASIA, TYPE 9"
+BMGC_DS15468,BMG_DS058287,ABDOMINAL OBESITY-METABOLIC SYNDROME 3
+BMGC_DS15469,BMG_DS058288,IMMUNODEFICIENCY 23
+BMGC_DS15470,BMG_DS058289,"intellectual disability, autosomal recessive 43"
+BMGC_DS15471,BMG_DS058290,"CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS"
+BMGC_DS15472,BMG_DS058291,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7"
+BMGC_DS15473,BMG_DS058292,VULTO-VAN SILFHOUT-DE VRIES SYNDROME
+BMGC_DS15474,BMG_DS058293,"AHDC1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome"
+BMGC_DS15475,BMG_DS058294,"PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4"
+BMGC_DS15476,BMG_DS058295,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 21
+BMGC_DS15477,BMG_DS058296,autism spectrum disorder due to AUTS2 deficiency
+BMGC_DS15478,BMG_DS058298,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8"
+BMGC_DS15479,BMG_DS058299,SPERMATOGENIC FAILURE 13
+BMGC_DS15480,BMG_DS058300,SPERMATOGENIC FAILURE 14
+BMGC_DS15481,BMG_DS058301,tumor predisposition syndrome 3
+BMGC_DS15482,BMG_DS058302,postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome
+BMGC_DS15483,BMG_DS058303,"PONTOCEREBELLAR HYPOPLASIA, TYPE 2E"
+BMGC_DS15484,BMG_DS058304,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 23
+BMGC_DS15485,BMG_DS058305,CONE-ROD DYSTROPHY 19
+BMGC_DS15486,BMG_DS058306,"NEPHROTIC SYNDROME, TYPE 10"
+BMGC_DS15487,BMG_DS058307,"DIARRHEA 7, PROTEIN-LOSING ENTEROPATHY TYPE"
+BMGC_DS15488,BMG_DS058308,COFFIN-SIRIS SYNDROME 9
+BMGC_DS15489,BMG_DS058309,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 24
+BMGC_DS15490,BMG_DS058310,primary ciliary dyskinesia 29
+BMGC_DS15491,BMG_DS058311,"ADNP-related multiple congenital anomalies, intellectual disability, autism spectrum disorder"
+BMGC_DS15492,BMG_DS058312,MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME
+BMGC_DS15493,BMG_DS058313,Tatton Brown Rahman syndrome
+BMGC_DS15494,BMG_DS058314,"MYOPATHY, TUBULAR AGGREGATE, 2"
+BMGC_DS15495,BMG_DS058315,HYPOTRICHOSIS 12
+BMGC_DS15496,BMG_DS058316,"AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5"
+BMGC_DS15497,BMG_DS058317,"BLEEDING DISORDER, PLATELET-TYPE, 18"
+BMGC_DS15498,BMG_DS058318,"LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE"
+BMGC_DS15499,BMG_DS058319,familial median cleft of the upper and lower lips
+BMGC_DS15500,BMG_DS058320,POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY
+BMGC_DS15501,BMG_DS058321,HYPOTRICHOSIS 13
+BMGC_DS15502,BMG_DS058322,IMMUNODEFICIENCY 24
+BMGC_DS15503,BMG_DS058323,"developmental and epileptic encephalopathy, 25"
+BMGC_DS15504,BMG_DS058324,DIAMOND-BLACKFAN ANEMIA 13
+BMGC_DS15505,BMG_DS058325,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2
+BMGC_DS15506,BMG_DS058327,"CARDIOMYOPATHY, DILATED, 1NN"
+BMGC_DS15507,BMG_DS058328,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20
+BMGC_DS15508,BMG_DS058329,ATAXIA-TELANGIECTASIA-LIKE DISORDER 2
+BMGC_DS15509,BMG_DS058330,RETINITIS PIGMENTOSA 70
+BMGC_DS15510,BMG_DS058331,"EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE"
+BMGC_DS15511,BMG_DS058332,"ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY"
+BMGC_DS15512,BMG_DS058333,WEBB-DATTANI SYNDROME
+BMGC_DS15513,BMG_DS058334,"STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET"
+BMGC_DS15514,BMG_DS058335,PANCREATIC AGENESIS 2
+BMGC_DS15515,BMG_DS058336,MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2
+BMGC_DS15516,BMG_DS058338,MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3
+BMGC_DS15517,BMG_DS058339,"intellectual disability, autosomal recessive 44"
+BMGC_DS15518,BMG_DS058340,"MYOPIA 24, AUTOSOMAL DOMINANT"
+BMGC_DS15519,BMG_DS058341,"HYPERLIPOPROTEINEMIA, TYPE ID"
+BMGC_DS15520,BMG_DS058342,"AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1"
+BMGC_DS15521,BMG_DS058343,ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2
+BMGC_DS15522,BMG_DS058344,"MYOPATHY, CENTRONUCLEAR, 5"
+BMGC_DS15523,BMG_DS058345,"Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome"
+BMGC_DS15524,BMG_DS058346,VESICOURETERAL REFLUX 8
+BMGC_DS15525,BMG_DS058347,IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES
+BMGC_DS15526,BMG_DS058348,NANOPHTHALMOS 4
+BMGC_DS15527,BMG_DS058349,CONE-ROD DYSTROPHY 20
+BMGC_DS15528,BMG_DS058350,IMMUNODEFICIENCY 27B
+BMGC_DS15529,BMG_DS058351,"intellectual disability, autosomal recessive 45"
+BMGC_DS15530,BMG_DS058352,LIPE-related familial partial lipodystrophy
+BMGC_DS15531,BMG_DS058354,"breasts and/or nipples, aplasia or hypoplasia of, 2"
+BMGC_DS15532,BMG_DS058355,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7
+BMGC_DS15533,BMG_DS058356,immunodeficiency 36
+BMGC_DS15534,BMG_DS058358,HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2
+BMGC_DS15535,BMG_DS058359,"Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome"
+BMGC_DS15536,BMG_DS058360,autosomal recessive severe congenital neutropenia due to JAGN1 deficiency
+BMGC_DS15537,BMG_DS058361,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11
+BMGC_DS15538,BMG_DS058362,FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG
+BMGC_DS15539,BMG_DS058363,ADAMS-OLIVER SYNDROME 5
+BMGC_DS15540,BMG_DS058365,"Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome"
+BMGC_DS15541,BMG_DS058366,HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA
+BMGC_DS15542,BMG_DS058367,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8
+BMGC_DS15543,BMG_DS058368,"MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1"
+BMGC_DS15544,BMG_DS058371,"CILIARY DYSKINESIA, PRIMARY, 30"
+BMGC_DS15545,BMG_DS058372,NEU-LAXOVA SYNDROME 2
+BMGC_DS15546,BMG_DS058373,"MYASTHENIC SYNDROME, CONGENITAL, 7A, PRESYNAPTIC, AND DISTAL MOTOR NEUROPATHY, AUTOSOMAL DOMINANT"
+BMGC_DS15547,BMG_DS058374,"DEAFNESS, AUTOSOMAL RECESSIVE 103"
+BMGC_DS15548,BMG_DS058376,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22
+BMGC_DS15549,BMG_DS058377,periodic fever-infantile enterocolitis-autoinflammatory syndrome
+BMGC_DS15550,BMG_DS058378,"MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS15551,BMG_DS058382,Episodic ataxia with slurred speech
+BMGC_DS15552,BMG_DS058383,"developmental and epileptic encephalopathy, 26"
+BMGC_DS15553,BMG_DS058384,MIRROR MOVEMENTS 3
+BMGC_DS15554,BMG_DS058385,"POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE"
+BMGC_DS15555,BMG_DS058386,"46,XY SEX REVERSAL 9"
+BMGC_DS15556,BMG_DS058387,"INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2"
+BMGC_DS15557,BMG_DS058388,"intellectual disability, autosomal dominant 29"
+BMGC_DS15558,BMG_DS058389,retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies
+BMGC_DS15559,BMG_DS058390,"MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS15560,BMG_DS058391,"PONTOCEREBELLAR HYPOPLASIA, TYPE 1C"
+BMGC_DS15561,BMG_DS058392,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 30, WITH SPEECH DELAY AND BEHAVIORAL ABNORMALITIES"
+BMGC_DS15562,BMG_DS058393,"SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY"
+BMGC_DS15563,BMG_DS058394,TYPE 2 DIABETES 5
+BMGC_DS15564,BMG_DS058395,Limb girdle muscular dystrophy due to POMK deficiency
+BMGC_DS15565,BMG_DS058396,Ketoacidosis due to monocarboxylate transporter-1 deficiency
+BMGC_DS15566,BMG_DS058397,IMMUNODEFICIENCY 37
+BMGC_DS15567,BMG_DS058398,PALMOPLANTAR KERATODERMA AND WOOLLY HAIR
+BMGC_DS15568,BMG_DS058399,autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
+BMGC_DS15569,BMG_DS058401,"psoriasis 15, pustular, susceptibility to"
+BMGC_DS15570,BMG_DS058402,"Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome"
+BMGC_DS15571,BMG_DS058403,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9"
+BMGC_DS15572,BMG_DS058404,Polyendocrine polyneuropathy syndrome
+BMGC_DS15573,BMG_DS058405,FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4
+BMGC_DS15574,BMG_DS058406,"intellectual disability, autosomal recessive 46"
+BMGC_DS15575,BMG_DS058407,CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY
+BMGC_DS15576,BMG_DS058408,"MACULAR DEGENERATION, EARLY-ONSET"
+BMGC_DS15577,BMG_DS058409,IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION
+BMGC_DS15578,BMG_DS058411,Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency
+BMGC_DS15579,BMG_DS058412,PERRAULT SYNDROME 5
+BMGC_DS15580,BMG_DS058413,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27"
+BMGC_DS15581,BMG_DS058414,RARS-related autosomal recessive hypomyelinating leukodystrophy
+BMGC_DS15582,BMG_DS058416,"MACULAR DYSTROPHY, VITELLIFORM, 4"
+BMGC_DS15583,BMG_DS058417,"MACULAR DYSTROPHY, VITELLIFORM, 5"
+BMGC_DS15584,BMG_DS058418,Fatty acyl-CoA reductase 1 deficiency
+BMGC_DS15585,BMG_DS058419,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S"
+BMGC_DS15586,BMG_DS058420,"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES"
+BMGC_DS15587,BMG_DS058421,NEMALINE MYOPATHY 10
+BMGC_DS15588,BMG_DS058422,"AORTIC ANEURYSM, FAMILIAL THORACIC 9"
+BMGC_DS15589,BMG_DS058423,MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT
+BMGC_DS15590,BMG_DS058424,"MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2"
+BMGC_DS15591,BMG_DS058425,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9"
+BMGC_DS15592,BMG_DS058426,"BLEEDING DISORDER, PLATELET-TYPE, 19"
+BMGC_DS15593,BMG_DS058427,OVARIAN DYSGENESIS 4
+BMGC_DS15594,BMG_DS058428,Progressive myoclonic epilepsy type 7
+BMGC_DS15595,BMG_DS058429,RETINAL DYSTROPHY AND OBESITY
+BMGC_DS15596,BMG_DS058430,"Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome"
+BMGC_DS15597,BMG_DS058432,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 47"
+BMGC_DS15598,BMG_DS058433,Polyglucosan body myopathy type 2
+BMGC_DS15599,BMG_DS058434,"Progeroid features, hepatocellular carcinoma predisposition syndrome"
+BMGC_DS15600,BMG_DS058435,Chronic atrial and intestinal dysrhythmia
+BMGC_DS15601,BMG_DS058437,CEREBELLOFACIODENTAL SYNDROME
+BMGC_DS15602,BMG_DS058438,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18"
+BMGC_DS15603,BMG_DS058439,AMYOTROPHIC LATERAL SCLEROSIS 22 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA
+BMGC_DS15604,BMG_DS058440,Autosomal dominant mitochondrial myopathy with exercise intolerance
+BMGC_DS15605,BMG_DS058441,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28"
+BMGC_DS15606,BMG_DS058442,lissencephaly 6 with microcephaly
+BMGC_DS15607,BMG_DS058443,THROMBOCYTOPENIA 5
+BMGC_DS15608,BMG_DS058444,NEPHRONOPHTHISIS 19
+BMGC_DS15609,BMG_DS058445,"FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 5"
+BMGC_DS15610,BMG_DS058446,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 9
+BMGC_DS15611,BMG_DS058447,"AMELOGENESIS IMPERFECTA, TYPE IH"
+BMGC_DS15612,BMG_DS058448,Temple syndrome
+BMGC_DS15613,BMG_DS058449,"MYASTHENIC SYNDROME, CONGENITAL, 15"
+BMGC_DS15614,BMG_DS058450,"MYASTHENIC SYNDROME, CONGENITAL, 14"
+BMGC_DS15615,BMG_DS058451,"OSTEOGENESIS IMPERFECTA, TYPE XVI"
+BMGC_DS15616,BMG_DS058452,"MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES"
+BMGC_DS15617,BMG_DS058453,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T"
+BMGC_DS15618,BMG_DS058454,Combined oxidative phosphorylation defect type 24
+BMGC_DS15619,BMG_DS058455,LONG QT SYNDROME 14
+BMGC_DS15620,BMG_DS058456,LETHAL CONGENITAL CONTRACTURE SYNDROME 6
+BMGC_DS15621,BMG_DS058457,LONG QT SYNDROME 15
+BMGC_DS15622,BMG_DS058458,Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome
+BMGC_DS15623,BMG_DS058459,TENORIO SYNDROME
+BMGC_DS15624,BMG_DS058460,"NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET 1"
+BMGC_DS15625,BMG_DS058461,PEELING SKIN SYNDROME 3
+BMGC_DS15626,BMG_DS058464,"OSTEOGENESIS IMPERFECTA, MILD"
+BMGC_DS15627,BMG_DS058466,Neonatal Marfan syndrome
+BMGC_DS15628,BMG_DS058469,"ALPHA-THALASSEMIA, HMONG TYPE"
+BMGC_DS15629,BMG_DS058470,"EPIDERMOLYSIS BULLOSA SIMPLEX 2A, GENERALIZED SEVERE"
+BMGC_DS15630,BMG_DS058472,"exfoliation syndrome, susceptibility to"
+BMGC_DS15631,BMG_DS058474,Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
+BMGC_DS15632,BMG_DS058475,Autosomal recessive central core disease
+BMGC_DS15633,BMG_DS058476,"ANEMIA, PERINATAL HEMOLYTIC, FATAL OR NEAR-FATAL"
+BMGC_DS15634,BMG_DS058479,"RENAL TUBULAR ACIDOSIS, DISTAL, 2, WITH PROGRESSIVE SENSORINEURAL HEARING LOSS"
+BMGC_DS15635,BMG_DS058481,myelodysplastic syndrome with ring sideroblasts
+BMGC_DS15636,BMG_DS058484,IMMUNODEFICIENCY 32B
+BMGC_DS15637,BMG_DS058485,Imerslund-Grasbeck syndrome type 1
+BMGC_DS15638,BMG_DS058487,IMERSLUND-GRASBECK SYNDROME 2
+BMGC_DS15639,BMG_DS058488,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 5"
+BMGC_DS15640,BMG_DS058491,"GALACTOSEMIA III, SEVERE"
+BMGC_DS15641,BMG_DS058492,mild Canavan disease
+BMGC_DS15642,BMG_DS058493,"TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE"
+BMGC_DS15643,BMG_DS058495,"17-alpha-hydroxylase/17,20-lyase deficiency, combined partial"
+BMGC_DS15644,BMG_DS058498,"SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES"
+BMGC_DS15645,BMG_DS058501,HEINZ BODY HEMOLYTIC ANEMIA
+BMGC_DS15646,BMG_DS058502,"allergic rhinitis, susceptibility to"
+BMGC_DS15647,BMG_DS058520,Mitochondrial Dysfunction
+BMGC_DS15648,BMG_DS058521,Generalized myoclonic seizure
+BMGC_DS15649,BMG_DS058522,central nervous system disorder
+BMGC_DS15650,BMG_DS058523,liver disorder
+BMGC_DS15651,BMG_DS058525,ovarian disorder
+BMGC_DS15652,BMG_DS058541,Obstructive azoospermia
+BMGC_DS15653,BMG_DS058545,Thyroid hemiagenesis
+BMGC_DS15654,BMG_DS058554,Myoclonic absence seizure
+BMGC_DS15655,BMG_DS058558,acromial dimples
+BMGC_DS15656,BMG_DS058566,punctate palmoplantar keratoderma
+BMGC_DS15657,BMG_DS058567,"ectodermal dysplasia 4, hair/nail type"
+BMGC_DS15658,BMG_DS058568,Mixed demyelinating and axonal polyneuropathy
+BMGC_DS15659,BMG_DS058570,Lower limb amyotrophy
+BMGC_DS15660,BMG_DS058573,Proximal spinal muscular atrophy
+BMGC_DS15661,BMG_DS058574,Unilateral polymicrogyria
+BMGC_DS15662,BMG_DS058579,Vasculitis of large artery
+BMGC_DS15663,BMG_DS058581,Congenital lactic acidosis
+BMGC_DS15664,BMG_DS058582,hypertrichosis cubiti-short stature syndrome
+BMGC_DS15665,BMG_DS058586,specific learning disability
+BMGC_DS15666,BMG_DS058588,peripheral nervous system disorder
+BMGC_DS15667,BMG_DS058589,optic choroid disorder
+BMGC_DS15668,BMG_DS058621,Asthma-Chronic Obstructive Pulmonary Disease Overlap Syndrome
+BMGC_DS15669,BMG_DS058636,Gastric hemorrhage due to angiodysplasia of stomach
+BMGC_DS15670,BMG_DS058840,Acute Hypoxemic Respiratory Failure
+BMGC_DS15671,BMG_DS058948,Acute Hypercapnic Respiratory Failure
+BMGC_DS15672,BMG_DS058965,Bronchopneumonia caused by Haemophilus influenzae
+BMGC_DS15673,BMG_DS059003,"3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome"
+BMGC_DS15674,BMG_DS059148,"Cone-rod synaptic disorder, congenital nonprogressive"
+BMGC_DS15675,BMG_DS059341,Autosomal dominant hypocalcemia
+BMGC_DS15676,BMG_DS059342,beta-Mannosidosis
+BMGC_DS15677,BMG_DS059343,Hydronephrosis Due To Pujo
+BMGC_DS15678,BMG_DS059344,Chorioretinal atrophy
+BMGC_DS15679,BMG_DS059348,multiple endocrine neoplasia type 2
+BMGC_DS15680,BMG_DS059349,cervical cancer
+BMGC_DS15681,BMG_DS059352,Hypermethioninemia
+BMGC_DS15682,BMG_DS059353,Juvenile seropositive polyarthritis
+BMGC_DS15683,BMG_DS059354,Sphincter of Oddi Dyskinesia
+BMGC_DS15684,BMG_DS059355,SMARCB1-related schwannomatosis
+BMGC_DS15685,BMG_DS059357,CATARACT 40
+BMGC_DS15686,BMG_DS059359,cone-rod dystrophy 21
+BMGC_DS15687,BMG_DS059360,"alopecia, androgenetic, 1"
+BMGC_DS15688,BMG_DS059361,Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency
+BMGC_DS15689,BMG_DS059365,kidney medullary carcinoma
+BMGC_DS15690,BMG_DS059372,glucocorticoid deficiency 1
+BMGC_DS15691,BMG_DS059373,glucocorticoid deficiency 2
+BMGC_DS15692,BMG_DS059378,Pituitary stalk interruption syndrome
+BMGC_DS15693,BMG_DS059381,inherited obesity
+BMGC_DS15694,BMG_DS059382,microcystic/reticular schwannoma
+BMGC_DS15695,BMG_DS059384,Familial glucocorticoid deficiency
+BMGC_DS15696,BMG_DS059386,Congenital isolated adrenocorticotropic hormone deficiency
+BMGC_DS15697,BMG_DS059388,C3 glomerulonephritis
+BMGC_DS15698,BMG_DS059389,acute myeloid leukemia with MNX1-ETV6 fusion
+BMGC_DS15699,BMG_DS059590,Urinary tract infection caused by Klebsiella
+BMGC_DS15700,BMG_DS059722,Autosomal Dominant Hereditary Pancreatitis
+BMGC_DS15701,BMG_DS060005,Hyperammonemia Due to Carbamoyl Phosphate Synthetase 1 Deficiency
+BMGC_DS15702,BMG_DS060006,Porencephalic cyst
+BMGC_DS15703,BMG_DS060007,Porencephaly
+BMGC_DS15704,BMG_DS060008,"Thyrotropin deficiency, isolated"
+BMGC_DS15705,BMG_DS060009,Charcot-Marie-Tooth disease type 4
+BMGC_DS15706,BMG_DS060011,Bulbar palsy
+BMGC_DS15707,BMG_DS060012,Deaf Mutism
+BMGC_DS15708,BMG_DS060013,Onychomycosis due to dermatophyte
+BMGC_DS15709,BMG_DS060017,CHROMOSOME Xp22 DELETION SYNDROME
+BMGC_DS15710,BMG_DS060018,Necrotizing enterocolitis in fetus OR newborn
+BMGC_DS15711,BMG_DS060019,progressive muscular atrophy
+BMGC_DS15712,BMG_DS060020,Dupuytren's Disease
+BMGC_DS15713,BMG_DS060021,"Guillain-Barre Syndrome, Familial"
+BMGC_DS15714,BMG_DS060022,"Parkinson disease 11, autosomal dominant, susceptibility to"
+BMGC_DS15715,BMG_DS060023,SPONDYLOCOSTAL DYSOSTOSIS 5
+BMGC_DS15716,BMG_DS060025,"Alopecia, Male Pattern"
+BMGC_DS15717,BMG_DS060026,"Trichothiodystrophy, Nonphotosensitive 1"
+BMGC_DS15718,BMG_DS060027,"DEAFNESS, AUTOSOMAL DOMINANT 40"
+BMGC_DS15719,BMG_DS060028,"DEAFNESS, AUTOSOMAL RECESSIVE 97"
+BMGC_DS15720,BMG_DS060029,"DEAFNESS, AUTOSOMAL DOMINANT 67"
+BMGC_DS15721,BMG_DS060031,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U"
+BMGC_DS15722,BMG_DS060032,JOUBERT SYNDROME 23
+BMGC_DS15723,BMG_DS060033,"MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL"
+BMGC_DS15724,BMG_DS060034,"FANCONI ANEMIA, COMPLEMENTATION GROUP T"
+BMGC_DS15725,BMG_DS060035,JOUBERT SYNDROME 24
+BMGC_DS15726,BMG_DS060036,JOUBERT SYNDROME 25
+BMGC_DS15727,BMG_DS060037,JOUBERT SYNDROME 26
+BMGC_DS15728,BMG_DS060039,MEND SYNDROME
+BMGC_DS15729,BMG_DS060040,osteofibrous dysplasia
+BMGC_DS15730,BMG_DS060041,OPTIC ATROPHY 8
+BMGC_DS15731,BMG_DS060042,PAGET DISEASE OF BONE 6
+BMGC_DS15732,BMG_DS060043,"PAGET DISEASE OF BONE 2, EARLY-ONSET"
+BMGC_DS15733,BMG_DS060044,PAGET DISEASE OF BONE 3
+BMGC_DS15734,BMG_DS060046,"Fibromatosis, Palmar"
+BMGC_DS15735,BMG_DS060047,Carbamoyl Phosphate Synthase 1 Deficiency
+BMGC_DS15736,BMG_DS060048,Cone-Rod Dystrophies
+BMGC_DS15737,BMG_DS060049,AL-RAQAD SYNDROME
+BMGC_DS15738,BMG_DS060050,CHOPS SYNDROME
+BMGC_DS15739,BMG_DS060051,LUSCAN-LUMISH SYNDROME
+BMGC_DS15740,BMG_DS060055,Familial infantile bilateral striatal necrosis
+BMGC_DS15741,BMG_DS060060,non-immunoglobulin-mediated membranoproliferative glomerulonephritis
+BMGC_DS15742,BMG_DS060063,autosomal dominant cerebellar ataxia
+BMGC_DS15743,BMG_DS060068,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1"
+BMGC_DS15744,BMG_DS060069,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 9"
+BMGC_DS15745,BMG_DS060070,"ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY"
+BMGC_DS15746,BMG_DS060071,"intellectual disability, autosomal dominant 34"
+BMGC_DS15747,BMG_DS060072,FAMILIAL ADENOMATOUS POLYPOSIS 3
+BMGC_DS15748,BMG_DS060073,Spinocerebellar ataxia type 41
+BMGC_DS15749,BMG_DS060074,"REDUCING BODY MYOPATHY, X-LINKED 1B, WITH LATE CHILDHOOD OR ADULT ONSET"
+BMGC_DS15750,BMG_DS060075,NUDT15 deficiency
+BMGC_DS15751,BMG_DS060076,Complex lethal osteochondrodysplasia
+BMGC_DS15752,BMG_DS060077,MITOCHONDRIAL DNA DEPLETION SYNDROME 14 (CARDIOENCEPHALOMYOPATHIC TYPE)
+BMGC_DS15753,BMG_DS060078,"ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3"
+BMGC_DS15754,BMG_DS060079,"NEPHROTIC SYNDROME, TYPE 13"
+BMGC_DS15755,BMG_DS060080,"NEPHROTIC SYNDROME, TYPE 12"
+BMGC_DS15756,BMG_DS060081,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 52"
+BMGC_DS15757,BMG_DS060082,"ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 3"
+BMGC_DS15758,BMG_DS060083,"LEUKODYSTROPHY, HYPOMYELINATING, 13"
+BMGC_DS15759,BMG_DS060084,"CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION"
+BMGC_DS15760,BMG_DS060085,"IMMUNODEFICIENCY, COMMON VARIABLE, 13"
+BMGC_DS15761,BMG_DS060086,DDX41-related hematologic malignancy predisposition syndrome
+BMGC_DS15762,BMG_DS060087,SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2
+BMGC_DS15763,BMG_DS060088,SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1
+BMGC_DS15764,BMG_DS060089,Childhood-onset spasticity with hyperglycinemia
+BMGC_DS15765,BMG_DS060090,COWDEN SYNDROME 7
+BMGC_DS15766,BMG_DS060091,EVEN-plus syndrome
+BMGC_DS15767,BMG_DS060092,Progressive scapulohumeroperoneal distal myopathy
+BMGC_DS15768,BMG_DS060093,CATARACT 45
+BMGC_DS15769,BMG_DS060094,"BRACHYDACTYLY, TYPE A1, D"
+BMGC_DS15770,BMG_DS060095,PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis
+BMGC_DS15771,BMG_DS060096,autosomal recessive early-onset Parkinson disease 23
+BMGC_DS15772,BMG_DS060097,"EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE"
+BMGC_DS15773,BMG_DS060098,MEIER-GORLIN SYNDROME 6
+BMGC_DS15774,BMG_DS060099,TMEM199 congenital disorder of glycosylation
+BMGC_DS15775,BMG_DS060100,CCDC115 congenital disorder of glycosylation
+BMGC_DS15776,BMG_DS060101,LIMS2-related limb girdle muscular dystrophy
+BMGC_DS15777,BMG_DS060102,"Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome"
+BMGC_DS15778,BMG_DS060103,"IgA nephropathy, susceptibility to, 3"
+BMGC_DS15779,BMG_DS060104,"MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2"
+BMGC_DS15780,BMG_DS060105,"HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION"
+BMGC_DS15781,BMG_DS060106,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 15
+BMGC_DS15782,BMG_DS060107,HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 6
+BMGC_DS15783,BMG_DS060108,Lamb Shaffer syndrome
+BMGC_DS15784,BMG_DS060109,"HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2"
+BMGC_DS15785,BMG_DS060110,Spinocerebellar ataxia type 42
+BMGC_DS15786,BMG_DS060111,"neuroblastoma, susceptibility to, 7"
+BMGC_DS15787,BMG_DS060112,IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS
+BMGC_DS15788,BMG_DS060113,orofacial cleft 15
+BMGC_DS15789,BMG_DS060114,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 2
+BMGC_DS15790,BMG_DS060115,"CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2"
+BMGC_DS15791,BMG_DS060116,SECKEL SYNDROME 9
+BMGC_DS15792,BMG_DS060117,LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA
+BMGC_DS15793,BMG_DS060118,"WOOLLY HAIR, AUTOSOMAL RECESSIVE 3"
+BMGC_DS15794,BMG_DS060119,SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES
+BMGC_DS15795,BMG_DS060120,"HETEROTAXY, VISCERAL, 7, AUTOSOMAL"
+BMGC_DS15796,BMG_DS060121,"AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE 1"
+BMGC_DS15797,BMG_DS060122,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 51"
+BMGC_DS15798,BMG_DS060123,RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2
+BMGC_DS15799,BMG_DS060124,"Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome"
+BMGC_DS15800,BMG_DS060125,"TREMOR, HEREDITARY ESSENTIAL, 5"
+BMGC_DS15801,BMG_DS060126,"skin creases, congenital symmetric circumferential, 2"
+BMGC_DS15802,BMG_DS060127,"COENZYME Q10 DEFICIENCY, PRIMARY, 8"
+BMGC_DS15803,BMG_DS060128,"OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES"
+BMGC_DS15804,BMG_DS060129,"NEPHROTIC SYNDROME, TYPE 11"
+BMGC_DS15805,BMG_DS060130,"CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES"
+BMGC_DS15806,BMG_DS060131,"CILIARY DYSKINESIA, PRIMARY, 33"
+BMGC_DS15807,BMG_DS060132,"TOOTH AGENESIS, SELECTIVE, 7"
+BMGC_DS15808,BMG_DS060133,SLC39A8 congenital disorder of glycosylation
+BMGC_DS15809,BMG_DS060134,"MYASTHENIC SYNDROME, CONGENITAL, 19"
+BMGC_DS15810,BMG_DS060135,rhizomelic chondrodysplasia punctata type 5
+BMGC_DS15811,BMG_DS060136,"PARKINSON DISEASE 22, AUTOSOMAL DOMINANT"
+BMGC_DS15812,BMG_DS060137,DESANTO-SHINAWI SYNDROME
+BMGC_DS15813,BMG_DS060138,"DEAFNESS, AUTOSOMAL DOMINANT 68"
+BMGC_DS15814,BMG_DS060139,"DEAFNESS, AUTOSOMAL DOMINANT 69"
+BMGC_DS15815,BMG_DS060140,DEHYDRATED HEREDITARY STOMATOCYTOSIS 2
+BMGC_DS15816,BMG_DS060141,"epilepsy, idiopathic generalized, susceptibility to, 14"
+BMGC_DS15817,BMG_DS060142,SURF1-related Charcot-Marie-Tooth disease type 4
+BMGC_DS15818,BMG_DS060143,"LEUKODYSTROPHY, HYPOMYELINATING, 12"
+BMGC_DS15819,BMG_DS060144,"Seizures, scoliosis, macrocephaly syndrome"
+BMGC_DS15820,BMG_DS060145,"MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS15821,BMG_DS060146,"SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE"
+BMGC_DS15822,BMG_DS060147,IMMUNODEFICIENCY 45
+BMGC_DS15823,BMG_DS060148,"Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome"
+BMGC_DS15824,BMG_DS060149,PMP22-RAI1 contiguous gene duplication syndrome
+BMGC_DS15825,BMG_DS060150,ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement
+BMGC_DS15826,BMG_DS060151,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 34
+BMGC_DS15827,BMG_DS060152,"EPILEPSY, PROGRESSIVE MYOCLONIC, 10"
+BMGC_DS15828,BMG_DS060153,"Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome"
+BMGC_DS15829,BMG_DS060154,IMMUNODEFICIENCY 44
+BMGC_DS15830,BMG_DS060155,"POROKERATOSIS 9, MULTIPLE TYPES"
+BMGC_DS15831,BMG_DS060156,SENIOR-LOKEN SYNDROME 9
+BMGC_DS15832,BMG_DS060157,HEIMLER SYNDROME 2
+BMGC_DS15833,BMG_DS060158,"CUTIS LAXA, AUTOSOMAL DOMINANT 3"
+BMGC_DS15834,BMG_DS060159,CRANIOSYNOSTOSIS 6
+BMGC_DS15835,BMG_DS060160,Kosaki overgrowth syndrome
+BMGC_DS15836,BMG_DS060161,ADAMS-OLIVER SYNDROME 6
+BMGC_DS15837,BMG_DS060162,Spondyloepiphyseal dysplasia Stanescu type
+BMGC_DS15838,BMG_DS060163,Au-Kline syndrome
+BMGC_DS15839,BMG_DS060164,"Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome"
+BMGC_DS15840,BMG_DS060165,"IMMUNODEFICIENCY, COMMON VARIABLE, 12, WITH AUTOIMMUNITY"
+BMGC_DS15841,BMG_DS060166,"SPONDYLOCOSTAL DYSOSTOSIS 6, AUTOSOMAL RECESSIVE"
+BMGC_DS15842,BMG_DS060167,NOONAN SYNDROME 10
+BMGC_DS15843,BMG_DS060168,RETINITIS PIGMENTOSA 74
+BMGC_DS15844,BMG_DS060169,NOONAN SYNDROME 9
+BMGC_DS15845,BMG_DS060170,"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 7"
+BMGC_DS15846,BMG_DS060171,"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6"
+BMGC_DS15847,BMG_DS060172,"Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome"
+BMGC_DS15848,BMG_DS060173,SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY
+BMGC_DS15849,BMG_DS060174,RETINITIS PIGMENTOSA 73
+BMGC_DS15850,BMG_DS060175,"SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION"
+BMGC_DS15851,BMG_DS060176,Progressive myoclonic epilepsy type 9
+BMGC_DS15852,BMG_DS060177,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9"
+BMGC_DS15853,BMG_DS060178,"thyroid cancer, nonmedullary, 5"
+BMGC_DS15854,BMG_DS060179,"thyroid cancer, nonmedullary, 4"
+BMGC_DS15855,BMG_DS060180,"herpes simplex encephalitis, susceptibility to, 7"
+BMGC_DS15856,BMG_DS060181,"NEURODEVELOPMENTAL DISORDER WITH SPASTICITY, HYPOMYELINATING LEUKODYSTROPHY, AND BRAIN ABNORMALITIES"
+BMGC_DS15857,BMG_DS060182,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 39"
+BMGC_DS15858,BMG_DS060183,ACHROMATOPSIA 7
+BMGC_DS15859,BMG_DS060184,"DEAFNESS, AUTOSOMAL RECESSIVE 104"
+BMGC_DS15860,BMG_DS060185,"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 14"
+BMGC_DS15861,BMG_DS060186,CATARACT 44
+BMGC_DS15862,BMG_DS060187,"OSTEOGENESIS IMPERFECTA, TYPE XVII"
+BMGC_DS15863,BMG_DS060188,"NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB, WITH OPTIC ATROPHY"
+BMGC_DS15864,BMG_DS060189,LETHAL CONGENITAL CONTRACTURE SYNDROME 9
+BMGC_DS15865,BMG_DS060190,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 13"
+BMGC_DS15866,BMG_DS060191,"LEUKODYSTROPHY, HYPOMYELINATING, 11"
+BMGC_DS15867,BMG_DS060192,SILVER-RUSSELL SYNDROME 3
+BMGC_DS15868,BMG_DS060193,Hereditary sensory and autonomic neuropathy type 8
+BMGC_DS15869,BMG_DS060194,"EPIDERMOLYSIS BULLOSA SIMPLEX 5D, GENERALIZED INTERMEDIATE, AUTOSOMAL RECESSIVE"
+BMGC_DS15870,BMG_DS060195,"NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN IMAGING ABNORMALITIES"
+BMGC_DS15871,BMG_DS060196,"CILIARY DYSKINESIA, PRIMARY, 32"
+BMGC_DS15872,BMG_DS060197,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2"
+BMGC_DS15873,BMG_DS060198,BETHLEM MYOPATHY 2
+BMGC_DS15874,BMG_DS060199,ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2
+BMGC_DS15875,BMG_DS060200,RETINITIS PIGMENTOSA 72
+BMGC_DS15876,BMG_DS060201,EXUDATIVE VITREORETINOPATHY 6
+BMGC_DS15877,BMG_DS060202,"ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE"
+BMGC_DS15878,BMG_DS060203,"EPILEPSY, FAMILIAL TEMPORAL LOBE, 8"
+BMGC_DS15879,BMG_DS060204,"intellectual disability, autosomal recessive 50"
+BMGC_DS15880,BMG_DS060205,"CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation"
+BMGC_DS15881,BMG_DS060206,ZIMMERMANN-LABAND SYNDROME 2
+BMGC_DS15882,BMG_DS060207,Basel Vanagaite Smirin Yosef syndrome
+BMGC_DS15883,BMG_DS060208,"CANDIDIASIS, FAMILIAL, 9"
+BMGC_DS15884,BMG_DS060209,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4
+BMGC_DS15885,BMG_DS060210,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3
+BMGC_DS15886,BMG_DS060211,"EPILEPSY, FAMILIAL TEMPORAL LOBE, 7"
+BMGC_DS15887,BMG_DS060212,IMMUNODEFICIENCY 40
+BMGC_DS15888,BMG_DS060213,"microphthalmia, isolated, with coloboma 10"
+BMGC_DS15889,BMG_DS060214,"46,XY SEX REVERSAL 10"
+BMGC_DS15890,BMG_DS060215,"PYCR2-related microcephaly, progressive leukoencephalopathy"
+BMGC_DS15891,BMG_DS060216,"HYPOMAGNESEMIA, SEIZURES, AND IMPAIRED INTELLECTUAL DEVELOPMENT 1"
+BMGC_DS15892,BMG_DS060217,"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6"
+BMGC_DS15893,BMG_DS060218,DYSTONIA 27
+BMGC_DS15894,BMG_DS060219,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 33
+BMGC_DS15895,BMG_DS060220,"MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS15896,BMG_DS060221,"PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 2"
+BMGC_DS15897,BMG_DS060222,BRUGADA SYNDROME 9
+BMGC_DS15898,BMG_DS060223,"DYSTONIA 26, MYOCLONIC"
+BMGC_DS15899,BMG_DS060224,RETINITIS PIGMENTOSA 71
+BMGC_DS15900,BMG_DS060225,"intellectual disability, autosomal dominant 38"
+BMGC_DS15901,BMG_DS060226,"TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE"
+BMGC_DS15902,BMG_DS060227,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G"
+BMGC_DS15903,BMG_DS060228,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 3"
+BMGC_DS15904,BMG_DS060229,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 4"
+BMGC_DS15905,BMG_DS060230,Multiple mitochondrial dysfunctions syndrome type 4
+BMGC_DS15906,BMG_DS060231,Mandibulofacial dysostosis with alopecia
+BMGC_DS15907,BMG_DS060232,"developmental and epileptic encephalopathy, 32"
+BMGC_DS15908,BMG_DS060233,White Sutton syndrome
+BMGC_DS15909,BMG_DS060234,"Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome"
+BMGC_DS15910,BMG_DS060235,PARKINSON DISEASE 21
+BMGC_DS15911,BMG_DS060236,"Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome"
+BMGC_DS15912,BMG_DS060237,"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6"
+BMGC_DS15913,BMG_DS060238,"developmental and epileptic encephalopathy, 31A"
+BMGC_DS15914,BMG_DS060239,IMMUNODEFICIENCY 39
+BMGC_DS15915,BMG_DS060240,LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA
+BMGC_DS15916,BMG_DS060241,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 30
+BMGC_DS15917,BMG_DS060242,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 29
+BMGC_DS15918,BMG_DS060243,"MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3"
+BMGC_DS15919,BMG_DS060244,"ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2"
+BMGC_DS15920,BMG_DS060245,"MYASTHENIC SYNDROME, CONGENITAL, 18"
+BMGC_DS15921,BMG_DS060246,"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13"
+BMGC_DS15922,BMG_DS060247,"MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY"
+BMGC_DS15923,BMG_DS060248,"MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY"
+BMGC_DS15924,BMG_DS060249,"MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL"
+BMGC_DS15925,BMG_DS060250,"MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY"
+BMGC_DS15926,BMG_DS060251,"MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL"
+BMGC_DS15927,BMG_DS060252,"MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL"
+BMGC_DS15928,BMG_DS060253,"MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY"
+BMGC_DS15929,BMG_DS060254,"MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL"
+BMGC_DS15930,BMG_DS060255,"intellectual disability, autosomal dominant 33"
+BMGC_DS15931,BMG_DS060256,SENIOR-LOKEN SYNDROME 8
+BMGC_DS15932,BMG_DS060257,"MYASTHENIC SYNDROME, CONGENITAL, 17"
+BMGC_DS15933,BMG_DS060258,SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY
+BMGC_DS15934,BMG_DS060259,LIPOYLTRANSFERASE 1 DEFICIENCY
+BMGC_DS15935,BMG_DS060260,SINGLETON-MERTEN SYNDROME 2
+BMGC_DS15936,BMG_DS060261,PLACK syndrome
+BMGC_DS15937,BMG_DS060262,COLE-CARPENTER SYNDROME 2
+BMGC_DS15938,BMG_DS060263,"Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome"
+BMGC_DS15939,BMG_DS060264,OPTIC ATROPHY 9
+BMGC_DS15940,BMG_DS060265,LETHAL CONGENITAL CONTRACTURE SYNDROME 8
+BMGC_DS15941,BMG_DS060266,LETHAL CONGENITAL CONTRACTURE SYNDROME 7
+BMGC_DS15942,BMG_DS060267,NEURODEVELOPMENTAL DISORDER WITH SPASTIC PARAPLEGIA AND MICROCEPHALY
+BMGC_DS15943,BMG_DS060268,CATARACT 43
+BMGC_DS15944,BMG_DS060269,congenital bile acid synthesis defect 5
+BMGC_DS15945,BMG_DS060270,MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
+BMGC_DS15946,BMG_DS060271,3-methylglutaconic aciduria type 7
+BMGC_DS15947,BMG_DS060272,"AMELOGENESIS IMPERFECTA, TYPE IF"
+BMGC_DS15948,BMG_DS060273,"Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome"
+BMGC_DS15949,BMG_DS060274,"Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome"
+BMGC_DS15950,BMG_DS060275,ATAXIA-OCULOMOTOR APRAXIA 4
+BMGC_DS15951,BMG_DS060276,"Congenital contracture of limbs and face, hypotonia, developmental delay syndrome"
+BMGC_DS15952,BMG_DS060277,SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES
+BMGC_DS15953,BMG_DS060278,Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency
+BMGC_DS15954,BMG_DS060279,PREMATURE OVARIAN FAILURE 10
+BMGC_DS15955,BMG_DS060280,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 23, WITH OR WITHOUT VENTRICULAR NONCOMPACTION"
+BMGC_DS15956,BMG_DS060281,"ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE"
+BMGC_DS15957,BMG_DS060282,"MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL"
+BMGC_DS15958,BMG_DS060283,PEELING SKIN SYNDROME 4
+BMGC_DS15959,BMG_DS060284,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25"
+BMGC_DS15960,BMG_DS060285,"thyroid cancer, nonmedullary, 3"
+BMGC_DS15961,BMG_DS060286,DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS
+BMGC_DS15962,BMG_DS060287,Spondylo-ocular syndrome
+BMGC_DS15963,BMG_DS060288,"MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL"
+BMGC_DS15964,BMG_DS060289,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 24"
+BMGC_DS15965,BMG_DS060290,"MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3"
+BMGC_DS15966,BMG_DS060291,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED"
+BMGC_DS15967,BMG_DS060292,syndromic X-linked intellectual disability 34
+BMGC_DS15968,BMG_DS060293,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33"
+BMGC_DS15969,BMG_DS060294,RITSCHER-SCHINZEL SYNDROME 2
+BMGC_DS15970,BMG_DS060295,"TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE"
+BMGC_DS15971,BMG_DS060296,LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3
+BMGC_DS15972,BMG_DS060297,DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS
+BMGC_DS15973,BMG_DS060298,"REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET"
+BMGC_DS15974,BMG_DS060299,"Colobomatous optic disc, macular atrophy, chorioretinopathy syndrome"
+BMGC_DS15975,BMG_DS060300,"ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY"
+BMGC_DS15976,BMG_DS060301,"thyroid cancer, nonmedullary, 2"
+BMGC_DS15977,BMG_DS060302,SINGLETON-MERTEN SYNDROME 1
+BMGC_DS15978,BMG_DS060303,"ANEMIA, SIDEROBLASTIC, 4"
+BMGC_DS15979,BMG_DS060304,Ehlers-Danlos syndrome classic type
+BMGC_DS15980,BMG_DS060305,CHROMOSOME 10p12-p11 DELETION SYNDROME
+BMGC_DS15981,BMG_DS060306,CHROMOSOME 2p25.3 DUPLICATION SYNDROME
+BMGC_DS15982,BMG_DS060307,CHROMOSOME 2p25.3 DELETION SYNDROME
+BMGC_DS15983,BMG_DS060308,"CHROMOSOME 5q14.3 DELETION SYNDROME, PROXIMAL"
+BMGC_DS15984,BMG_DS060309,"RETINAL DYSTROPHY, EARLY-ONSET, WITH OR WITHOUT PITUITARY DYSFUNCTION"
+BMGC_DS15985,BMG_DS060310,"EPILEPSY, PROGRESSIVE MYOCLONIC, WITH SENSORY ATAXIC NEUROPATHY"
+BMGC_DS15986,BMG_DS060311,"PLASMINOGEN DEFICIENCY, TYPE II"
+BMGC_DS15987,BMG_DS060312,14q32 duplication syndrome
+BMGC_DS15988,BMG_DS060313,CHROMOSOME 13q32 DELETION SYNDROME
+BMGC_DS15989,BMG_DS060314,"migraine, with or without aura, susceptibility to, 13"
+BMGC_DS15990,BMG_DS060315,RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CATARACT
+BMGC_DS15991,BMG_DS060317,"MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES"
+BMGC_DS15992,BMG_DS060318,SPERMATOGENIC FAILURE 6
+BMGC_DS15993,BMG_DS060320,IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH CARDIAC DEFECTS
+BMGC_DS15994,BMG_DS060331,"ANEMIA, SIDEROBLASTIC, 1, LATE-ONSET"
+BMGC_DS15995,BMG_DS060339,CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME
+BMGC_DS15996,BMG_DS060341,VACTERL/vater association
+BMGC_DS15997,BMG_DS060394,Isolated polycystic liver disease
+BMGC_DS15998,BMG_DS060396,Bilateral Vestibulopathy
+BMGC_DS15999,BMG_DS060614,Colonic inflammatory bowel disease unclassified (IBDU)
+BMGC_DS16000,BMG_DS060659,Celiac disease with steatorrhea
+BMGC_DS16001,BMG_DS060756,autosomal recessive osteopetrosis
+BMGC_DS16002,BMG_DS060760,Branchiootic syndrome
+BMGC_DS16003,BMG_DS060773,Proximal 16p11.2 microdeletion syndrome
+BMGC_DS16004,BMG_DS060776,TMEM70 related mitochondrial encephalo-cardio-myopathy
+BMGC_DS16005,BMG_DS060779,Hypothyroidism due to mutation in transcription factor of pituitary development
+BMGC_DS16006,BMG_DS060785,Genetic steroid-resistant nephrotic syndrome
+BMGC_DS16007,BMG_DS060786,Fatal infantile cytochrome C oxidase deficiency
+BMGC_DS16008,BMG_DS060787,Combined pituitary hormone deficiency genetic form
+BMGC_DS16009,BMG_DS060788,Familial thyroid dyshormonogenesis
+BMGC_DS16010,BMG_DS060794,Fetal iodine syndrome
+BMGC_DS16011,BMG_DS060796,Distal monosomy 1q syndrome
+BMGC_DS16012,BMG_DS060798,Congenital plasminogen activator inhibitor deficiency type 1
+BMGC_DS16013,BMG_DS060803,Obesity due to melanocortin 4 receptor deficiency
+BMGC_DS16014,BMG_DS060812,Familial pseudohyperkalemia
+BMGC_DS16015,BMG_DS060816,Hereditary palmoplantar keratoderma Gamborg Nielsen type
+BMGC_DS16016,BMG_DS060817,Benign adult familial myoclonic epilepsy
+BMGC_DS16017,BMG_DS060820,Boichis syndrome
+BMGC_DS16018,BMG_DS060821,Hyperinsulinism due to deficiency of glucokinase
+BMGC_DS16019,BMG_DS060824,Renal tubulopathy with encephalopathy and liver failure syndrome
+BMGC_DS16020,BMG_DS060825,Autosomal recessive sideroblastic anemia
+BMGC_DS16021,BMG_DS060826,Hyperinsulinism due to HNF4A deficiency
+BMGC_DS16022,BMG_DS060828,Autosomal dominant hyperinsulinism due to SUR1 deficiency
+BMGC_DS16023,BMG_DS060829,Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
+BMGC_DS16024,BMG_DS060832,Pelizaeus Merzbacher like disease
+BMGC_DS16025,BMG_DS060833,Syndromic recessive X-linked ichthyosis
+BMGC_DS16026,BMG_DS060834,Joubert syndrome with renal defect
+BMGC_DS16027,BMG_DS060835,Joubert syndrome with ocular defect
+BMGC_DS16028,BMG_DS060843,Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency
+BMGC_DS16029,BMG_DS060847,nanophthalmia
+BMGC_DS16030,BMG_DS060853,Congenital alpha-2-antiplasmin deficiency
+BMGC_DS16031,BMG_DS060855,Familial non-autoimmune autosomal dominant hyperthyroidism
+BMGC_DS16032,BMG_DS060858,hereditary recurrent myoglobinuria
+BMGC_DS16033,BMG_DS060861,FRAXF syndrome
+BMGC_DS16034,BMG_DS060863,Hereditary pheochromocytoma and paraganglioma
+BMGC_DS16035,BMG_DS060865,Congenital deficiency of alpha-fetoprotein
+BMGC_DS16036,BMG_DS060872,Autosomal dominant late onset Parkinson disease
+BMGC_DS16037,BMG_DS060910,Autosomal dominant spondylocostal dysostosis
+BMGC_DS16038,BMG_DS060918,Mendelian susceptibility to mycobacterial disease due to complete IL12RB1 deficiency
+BMGC_DS16039,BMG_DS060920,Morse Rawnsley Sargent syndrome
+BMGC_DS16040,BMG_DS060928,Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type
+BMGC_DS16041,BMG_DS060935,Gingival fibromatosis and hypertrichosis syndrome
+BMGC_DS16042,BMG_DS060943,Familial isolated arrhythmogenic right ventricular dysplasia
+BMGC_DS16043,BMG_DS060955,Lissencephaly with cerebellar hypoplasia
+BMGC_DS16044,BMG_DS060957,Acetazolamide responsive myotonia
+BMGC_DS16045,BMG_DS060958,Lissencephaly type 1 due to doublecortin gene mutation
+BMGC_DS16046,BMG_DS060962,maternal uniparental disomy of chromosome 20
+BMGC_DS16047,BMG_DS060963,Intestinal epithelial dysplasia
+BMGC_DS16048,BMG_DS060964,Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early onset osteoarthritis
+BMGC_DS16049,BMG_DS060967,Familial avascular necrosis of femoral head
+BMGC_DS16050,BMG_DS060968,Transthyretin related familial amyloid cardiomyopathy
+BMGC_DS16051,BMG_DS060970,Desmin related myopathy with Mallory body-like inclusions
+BMGC_DS16052,BMG_DS060971,Atypical Werner syndrome
+BMGC_DS16053,BMG_DS060984,Infection of skin of eyelid and periocular region
+BMGC_DS16054,BMG_DS060986,Familial abdominal aortic aneurysm
+BMGC_DS16055,BMG_DS060987,Young onset Parkinson disease
+BMGC_DS16056,BMG_DS060989,Fatal infantile lactic acidosis with methylmalonic aciduria
+BMGC_DS16057,BMG_DS060990,X-linked retinal dysplasia
+BMGC_DS16058,BMG_DS060994,Familial spontaneous pneumothorax
+BMGC_DS16059,BMG_DS061002,Chemical and Drug Induced Liver Injury
+BMGC_DS16060,BMG_DS061003,ciliopathy
+BMGC_DS16061,BMG_DS061005,Chemically-Induced Liver Toxicity
+BMGC_DS16062,BMG_DS061162,frontometaphyseal dysplasia 1
+BMGC_DS16063,BMG_DS061164,Childhood Absence Epilepsy
+BMGC_DS16064,BMG_DS061167,PDA1
+BMGC_DS16065,BMG_DS061168,Alzheimer disease 9
+BMGC_DS16066,BMG_DS061169,Sialidase deficiency
+BMGC_DS16067,BMG_DS061170,"polydactyly, postaxial, type A1"
+BMGC_DS16068,BMG_DS061171,Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency
+BMGC_DS16069,BMG_DS061174,"DEAFNESS, AUTOSOMAL DOMINANT 66"
+BMGC_DS16070,BMG_DS061175,TONNE-KALSCHEUER SYNDROME
+BMGC_DS16071,BMG_DS061177,MIRAGE SYNDROME
+BMGC_DS16072,BMG_DS061178,"FANCONI ANEMIA, COMPLEMENTATION GROUP R"
+BMGC_DS16073,BMG_DS061180,"AORTIC ANEURYSM, FAMILIAL THORACIC 10"
+BMGC_DS16074,BMG_DS061181,"SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE"
+BMGC_DS16075,BMG_DS061182,"SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY"
+BMGC_DS16076,BMG_DS061183,BAND HETEROTOPIA
+BMGC_DS16077,BMG_DS061184,PATENT DUCTUS ARTERIOSUS 2
+BMGC_DS16078,BMG_DS061185,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1"
+BMGC_DS16079,BMG_DS061186,METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA
+BMGC_DS16080,BMG_DS061188,Post-Cardiac Arrest Syndrome
+BMGC_DS16081,BMG_DS061194,vulvar keratoacanthoma
+BMGC_DS16082,BMG_DS061202,ovarian endometrioid stromal and related neoplasms
+BMGC_DS16083,BMG_DS061205,RELA fusion-positive ependymoma
+BMGC_DS16084,BMG_DS061206,endometrioid stromal and related neoplasms of the vagina
+BMGC_DS16085,BMG_DS061207,endometrioid stromal and related neoplasms of the cervix
+BMGC_DS16086,BMG_DS061211,cervical villoglandular adenocarcinoma
+BMGC_DS16087,BMG_DS061216,deficiency of adenosine deaminase 2
+BMGC_DS16088,BMG_DS061217,acute flaccid myelitis
+BMGC_DS16089,BMG_DS061223,diseases of the central nervous system caused by prions
+BMGC_DS16090,BMG_DS061237,megaloblastic anemia unresponsive to vitamin B12 or folate therapy
+BMGC_DS16091,BMG_DS061239,diabetes (mellitus) due to autoimmune process
+BMGC_DS16092,BMG_DS061240,diabetes (mellitus) due to immune mediated pancreatic islet beta-cell destruction
+BMGC_DS16093,BMG_DS061241,idiopathic diabetes (mellitus)
+BMGC_DS16094,BMG_DS061242,diabetes (mellitus) due to insulin secretory defect
+BMGC_DS16095,BMG_DS061246,the listed conditions whether the disorder is in the pituitary or the hypothalamus
+BMGC_DS16096,BMG_DS061252,Alzheimer's dementia senile and presenile forms
+BMGC_DS16097,BMG_DS061277,endarteritis deformans or obliterans
+BMGC_DS16098,BMG_DS061339,Leser-Trélat disease
+BMGC_DS16099,BMG_DS061349,cervicothoracic disc disorders with cervicalgia
+BMGC_DS16100,BMG_DS061350,cervicothoracic disc disorders
+BMGC_DS16101,BMG_DS061370,hyperplastic polyposis syndrome
+BMGC_DS16102,BMG_DS061500,Cryptogenic multifocal ulcerous stenosing enteritis
+BMGC_DS16103,BMG_DS061566,X-linked congenital dyserythropoietic anemia with thrombocytopenia
+BMGC_DS16104,BMG_DS061576,"Juvenile cataract, microcornea, renal glucosuria syndrome"
+BMGC_DS16105,BMG_DS061579,Dystrophic epidermolysis bullosa nails only
+BMGC_DS16106,BMG_DS061580,Dysspondyloenchondromatosis
+BMGC_DS16107,BMG_DS061589,Congenital hereditary facial paralysis with variable hearing loss syndrome
+BMGC_DS16108,BMG_DS061599,Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
+BMGC_DS16109,BMG_DS061600,"Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome"
+BMGC_DS16110,BMG_DS061601,Autosomal dominant beta2-microglobulinic amyloidosis
+BMGC_DS16111,BMG_DS061602,Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome
+BMGC_DS16112,BMG_DS061607,"Agnathia, holoprosencephaly, situs inversus syndrome"
+BMGC_DS16113,BMG_DS061608,"Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome"
+BMGC_DS16114,BMG_DS061620,Severe X-linked mitochondrial encephalomyopathy
+BMGC_DS16115,BMG_DS061622,"Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome"
+BMGC_DS16116,BMG_DS061632,"Overgrowth, macrocephaly, facial dysmorphism syndrome"
+BMGC_DS16117,BMG_DS061635,"Osteosclerosis, developmental delay, craniosynostosis syndrome"
+BMGC_DS16118,BMG_DS061657,Obesity due to prohormone convertase I deficiency
+BMGC_DS16119,BMG_DS061667,"Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome"
+BMGC_DS16120,BMG_DS061746,Microduplication Xp11.22p11.23 syndrome
+BMGC_DS16121,BMG_DS061747,Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency
+BMGC_DS16122,BMG_DS061751,"Hyperuricemia, anemia, renal failure syndrome"
+BMGC_DS16123,BMG_DS061753,Hyperinsulinism due to uncoupling protein 2 deficiency
+BMGC_DS16124,BMG_DS061816,Otitis media caused by Streptococcus pneumoniae
+BMGC_DS16125,BMG_DS061928,systemic Epstein-Barr virus positive T-cell lymphoma of childhood
+BMGC_DS16126,BMG_DS061970,Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
+BMGC_DS16127,BMG_DS061971,Hyperinsulinism due to insulin receptor deficiency
+BMGC_DS16128,BMG_DS061972,Hyperinsulinism due to HNF1A deficiency
+BMGC_DS16129,BMG_DS061975,Homocystinuria without methylmalonic aciduria
+BMGC_DS16130,BMG_DS061977,Familial Alzheimer-like prion disease
+BMGC_DS16131,BMG_DS062019,Brain dopamine-serotonin vesicular transport disease
+BMGC_DS16132,BMG_DS062023,Bilateral microtia with deafness and cleft palate syndrome
+BMGC_DS16133,BMG_DS062024,COG4 congenital disorder of glycosylation
+BMGC_DS16134,BMG_DS062029,Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
+BMGC_DS16135,BMG_DS062037,"Developmental malformation, deafness, dystonia syndrome"
+BMGC_DS16136,BMG_DS062039,DEND syndrome
+BMGC_DS16137,BMG_DS062042,Short stature due to primary acid labile subunit deficiency
+BMGC_DS16138,BMG_DS062043,"Short stature, pituitary and cerebellar defect and small sella turcica syndrome"
+BMGC_DS16139,BMG_DS062046,Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency
+BMGC_DS16140,BMG_DS062051,Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome
+BMGC_DS16141,BMG_DS062083,"Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome"
+BMGC_DS16142,BMG_DS062092,Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3
+BMGC_DS16143,BMG_DS062093,Familial thrombocytosis
+BMGC_DS16144,BMG_DS062094,Encephalopathy due to prosaposin deficiency
+BMGC_DS16145,BMG_DS062096,Ehlers-Danlos syndrome kyphoscoliotic and deafness type
+BMGC_DS16146,BMG_DS062097,Ehlers-Danlos syndrome cardiac valvular type
+BMGC_DS16147,BMG_DS062099,"Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome"
+BMGC_DS16148,BMG_DS062101,Deficiency of cathepsin D
+BMGC_DS16149,BMG_DS062105,Craniofacial ulnar renal syndrome
+BMGC_DS16150,BMG_DS062128,Autosomal dominant macrothrombocytopenia
+BMGC_DS16151,BMG_DS062129,Attenuated Chédiak-Higashi syndrome
+BMGC_DS16152,BMG_DS062132,Deafness and myopia syndrome
+BMGC_DS16153,BMG_DS062142,Adult-onset autosomal recessive sideroblastic anemia
+BMGC_DS16154,BMG_DS062143,Adducted thumbs and arthrogryposis syndrome Christian type
+BMGC_DS16155,BMG_DS062144,Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein
+BMGC_DS16156,BMG_DS062165,Autosomal dominant limb girdle muscular dystrophy type 1A
+BMGC_DS16157,BMG_DS062170,Timothy syndrome type 2
+BMGC_DS16158,BMG_DS062172,Influenza caused by pandemic influenza virus
+BMGC_DS16159,BMG_DS062178,X-linked hereditary sensory and autonomic neuropathy with deafness
+BMGC_DS16160,BMG_DS062183,Xeroderma pigmentosum and Cockayne syndrome complex
+BMGC_DS16161,BMG_DS062191,Multiple epiphyseal dysplasia Al-Gazali type
+BMGC_DS16162,BMG_DS062195,8p11.2 deletion syndrome
+BMGC_DS16163,BMG_DS062197,6q terminal deletion syndrome
+BMGC_DS16164,BMG_DS062198,5q35 microduplication syndrome
+BMGC_DS16165,BMG_DS062201,5q14.3 microdeletion syndrome
+BMGC_DS16166,BMG_DS062203,2q32q33 microdeletion syndrome
+BMGC_DS16167,BMG_DS062204,2q23.1 microdeletion syndrome
+BMGC_DS16168,BMG_DS062205,2p21 microdeletion syndrome
+BMGC_DS16169,BMG_DS062207,20p12.3 microdeletion syndrome
+BMGC_DS16170,BMG_DS062208,1q44 microdeletion syndrome
+BMGC_DS16171,BMG_DS062210,1p21.3 microdeletion syndrome
+BMGC_DS16172,BMG_DS062212,Absence of fingerprints with congenital milia syndrome
+BMGC_DS16173,BMG_DS062215,17q23.1q23.2 microdeletion syndrome
+BMGC_DS16174,BMG_DS062226,17p13.3 microduplication syndrome
+BMGC_DS16175,BMG_DS062240,Benign concentric annular macular dystrophy
+BMGC_DS16176,BMG_DS062242,Autosomal dominant palmoplantar keratoderma and congenital alopecia
+BMGC_DS16177,BMG_DS062243,Autosomal dominant focal dystonia DYT25 type
+BMGC_DS16178,BMG_DS062244,Autosomal dominant Charcot-Marie-Tooth disease type 2M
+BMGC_DS16179,BMG_DS062245,Autosomal dominant Charcot-Marie-Tooth disease type 2L
+BMGC_DS16180,BMG_DS062247,Congenital bile acid synthesis defect type 3
+BMGC_DS16181,BMG_DS062250,Late-onset junctional epidermolysis bullosa
+BMGC_DS16182,BMG_DS062251,Leber plus disease
+BMGC_DS16183,BMG_DS062255,Leukoencephalopathy with metaphyseal chondrodysplasia syndrome
+BMGC_DS16184,BMG_DS062266,Primary ciliary dyskinesia and retinitis pigmentosa syndrome
+BMGC_DS16185,BMG_DS062267,Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome
+BMGC_DS16186,BMG_DS062268,Primary pigmented nodular adrenocortical disease
+BMGC_DS16187,BMG_DS062270,Progressive cavitating leukoencephalopathy
+BMGC_DS16188,BMG_DS062272,Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome
+BMGC_DS16189,BMG_DS062277,X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome
+BMGC_DS16190,BMG_DS062282,X-linked intellectual disability with cerebellar hypoplasia syndrome
+BMGC_DS16191,BMG_DS062291,VACTERL syndrome with hydrocephalus
+BMGC_DS16192,BMG_DS062292,Uveal coloboma with cleft lip and palate and intellectual disability syndrome
+BMGC_DS16193,BMG_DS062295,X-linked intellectual disability Cantagrel type
+BMGC_DS16194,BMG_DS062302,X-linked intellectual disability Van Esch type
+BMGC_DS16195,BMG_DS062305,X-linked intellectual disability Stocco Dos Santos type
+BMGC_DS16196,BMG_DS062307,X-linked intellectual disability Siderius type
+BMGC_DS16197,BMG_DS062309,Syndromic X-linked intellectual disability type 11
+BMGC_DS16198,BMG_DS062312,Chromosome Xq27.3q28 duplication syndrome
+BMGC_DS16199,BMG_DS062314,Cataract glaucoma syndrome
+BMGC_DS16200,BMG_DS062316,Fried syndrome
+BMGC_DS16201,BMG_DS062320,12q14 microdeletion syndrome
+BMGC_DS16202,BMG_DS062323,"Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome"
+BMGC_DS16203,BMG_DS062325,lissencephaly due to TUBA1A mutation
+BMGC_DS16204,BMG_DS062326,Isolated autosomal dominant hypomagnesemia Glaudemans type
+BMGC_DS16205,BMG_DS062330,15q14 microdeletion syndrome
+BMGC_DS16206,BMG_DS062331,14q12 microdeletion syndrome
+BMGC_DS16207,BMG_DS062332,Congenital analbuminemia
+BMGC_DS16208,BMG_DS062335,Primary immunodeficiency syndrome due to p14 deficiency
+BMGC_DS16209,BMG_DS062338,Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome
+BMGC_DS16210,BMG_DS062340,Congenital hypothyroidism due to absence of thyroid gland
+BMGC_DS16211,BMG_DS062342,Distal monosomy 10q syndrome
+BMGC_DS16212,BMG_DS062345,acral self-healing collodion baby
+BMGC_DS16213,BMG_DS062348,Moyamoya disease with early onset achalasia
+BMGC_DS16214,BMG_DS062352,Wartenberg Syndrome
+BMGC_DS16215,BMG_DS062410,Multi-Drug Resistant Nephrotic Syndrome
+BMGC_DS16216,BMG_DS062420,Mayer-Rokitansky-Küster-Hauser syndrome type 2
+BMGC_DS16217,BMG_DS062428,"Hypercalcemia, Infantile, 1"
+BMGC_DS16218,BMG_DS062429,"Hypercalcemia, infantile, 2"
+BMGC_DS16219,BMG_DS062431,OTU deubiquitinase with linear linkage specificity related autoinflammatory syndrome (disorder)
+BMGC_DS16220,BMG_DS062432,"ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE"
+BMGC_DS16221,BMG_DS062433,INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS
+BMGC_DS16222,BMG_DS062434,"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME"
+BMGC_DS16223,BMG_DS062435,"intellectual disability, autosomal recessive 59"
+BMGC_DS16224,BMG_DS062436,Yao syndrome
+BMGC_DS16225,BMG_DS062437,"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 12"
+BMGC_DS16226,BMG_DS062438,anterior segment dysgenesis 8
+BMGC_DS16227,BMG_DS062439,ANTERIOR SEGMENT DYSGENESIS 6
+BMGC_DS16228,BMG_DS062440,"BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6"
+BMGC_DS16229,BMG_DS062441,"COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS"
+BMGC_DS16230,BMG_DS062442,RETINITIS PIGMENTOSA 77
+BMGC_DS16231,BMG_DS062443,MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME
+BMGC_DS16232,BMG_DS062444,OPTIC ATROPHY 11
+BMGC_DS16233,BMG_DS062445,LYMPHATIC MALFORMATION 7
+BMGC_DS16234,BMG_DS062446,"amelogenesis imperfecta, type 1J"
+BMGC_DS16235,BMG_DS062447,"EPIDERMOLYSIS BULLOSA SIMPLEX 6, GENERALIZED INTERMEDIATE, WITH OR WITHOUT CARDIOMYOPATHY"
+BMGC_DS16236,BMG_DS062448,"EPILEPSY, EARLY-ONSET, 1, VITAMIN B6-DEPENDENT"
+BMGC_DS16237,BMG_DS062449,Dystonia 28
+BMGC_DS16238,BMG_DS062450,MEPAN syndrome
+BMGC_DS16239,BMG_DS062451,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 49
+BMGC_DS16240,BMG_DS062452,"ATRIAL FIBRILLATION, FAMILIAL, 18"
+BMGC_DS16241,BMG_DS062453,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 48
+BMGC_DS16242,BMG_DS062454,"tooth agenesis, selective, 9"
+BMGC_DS16243,BMG_DS062455,"GLAUCOMA 3, PRIMARY CONGENITAL, E"
+BMGC_DS16244,BMG_DS062456,NEPHRONOPHTHISIS 20
+BMGC_DS16245,BMG_DS062457,"intellectual disability, autosomal recessive 58"
+BMGC_DS16246,BMG_DS062458,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE"
+BMGC_DS16247,BMG_DS062459,"GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES"
+BMGC_DS16248,BMG_DS062460,"MYOPATHY, MYOFIBRILLAR, 8"
+BMGC_DS16249,BMG_DS062461,LISSENCEPHALY 8
+BMGC_DS16250,BMG_DS062462,SECKEL SYNDROME 10
+BMGC_DS16251,BMG_DS062463,UNCOMBABLE HAIR SYNDROME 3
+BMGC_DS16252,BMG_DS062464,UNCOMBABLE HAIR SYNDROME 2
+BMGC_DS16253,BMG_DS062465,"3-METHYLGLUTACONIC ACIDURIA, TYPE VIII"
+BMGC_DS16254,BMG_DS062466,"FANCONI ANEMIA, COMPLEMENTATION GROUP U"
+BMGC_DS16255,BMG_DS062467,"FANCONI ANEMIA, COMPLEMENTATION GROUP V"
+BMGC_DS16256,BMG_DS062468,"LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME"
+BMGC_DS16257,BMG_DS062469,"MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC"
+BMGC_DS16258,BMG_DS062470,"MYOPIA 25, AUTOSOMAL DOMINANT"
+BMGC_DS16259,BMG_DS062471,IMMUNODEFICIENCY 49
+BMGC_DS16260,BMG_DS062472,"MYOCLONUS, INTRACTABLE, NEONATAL"
+BMGC_DS16261,BMG_DS062473,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 16
+BMGC_DS16262,BMG_DS062474,POGLUT1-related limb girdle muscular dystrophy R21
+BMGC_DS16263,BMG_DS062475,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31
+BMGC_DS16264,BMG_DS062476,"SUDDEN CARDIAC FAILURE, ALCOHOL-INDUCED"
+BMGC_DS16265,BMG_DS062477,"SUDDEN CARDIAC FAILURE, INFANTILE"
+BMGC_DS16266,BMG_DS062478,"AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6"
+BMGC_DS16267,BMG_DS062479,SPERMATOGENIC FAILURE 17
+BMGC_DS16268,BMG_DS062480,"ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY"
+BMGC_DS16269,BMG_DS062481,"HETEROTAXY, VISCERAL, 8, AUTOSOMAL"
+BMGC_DS16270,BMG_DS062482,PERIVENTRICULAR NODULAR HETEROTOPIA 7
+BMGC_DS16271,BMG_DS062483,LETHAL CONGENITAL CONTRACTURE SYNDROME 11
+BMGC_DS16272,BMG_DS062484,SHASHI-PENA SYNDROME
+BMGC_DS16273,BMG_DS062485,"intellectual disability, autosomal recessive 57"
+BMGC_DS16274,BMG_DS062486,SPERMATOGENIC FAILURE 16
+BMGC_DS16275,BMG_DS062487,"ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY"
+BMGC_DS16276,BMG_DS062488,"MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT"
+BMGC_DS16277,BMG_DS062489,"Ocular anomalies, axonal neuropathy, developmental delay syndrome"
+BMGC_DS16278,BMG_DS062490,"LODDER-MERLA SYNDROME, TYPE 2, WITH DEVELOPMENTAL DELAY AND WITH OR WITHOUT CARDIAC ARRHYTHMIA"
+BMGC_DS16279,BMG_DS062491,CHITAYAT SYNDROME
+BMGC_DS16280,BMG_DS062492,RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES
+BMGC_DS16281,BMG_DS062493,"EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2"
+BMGC_DS16282,BMG_DS062494,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND IMPAIRED EXPRESSIVE LANGUAGE AND WITH OR WITHOUT SEIZURES
+BMGC_DS16283,BMG_DS062495,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 74"
+BMGC_DS16284,BMG_DS062496,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47"
+BMGC_DS16285,BMG_DS062497,SHORT STATURE-MICROGNATHIA SYNDROME
+BMGC_DS16286,BMG_DS062498,"developmental and epileptic encephalopathy, 46"
+BMGC_DS16287,BMG_DS062499,SIFRIM-HITZ-WEISS SYNDROME
+BMGC_DS16288,BMG_DS062500,"SHORT STATURE, BRACHYDACTYLY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES"
+BMGC_DS16289,BMG_DS062501,MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE)
+BMGC_DS16290,BMG_DS062502,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 45
+BMGC_DS16291,BMG_DS062503,"ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH"
+BMGC_DS16292,BMG_DS062504,"NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET"
+BMGC_DS16293,BMG_DS062505,"MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC"
+BMGC_DS16294,BMG_DS062506,aniridia 3
+BMGC_DS16295,BMG_DS062507,"Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome"
+BMGC_DS16296,BMG_DS062508,FRONTOMETAPHYSEAL DYSPLASIA 2
+BMGC_DS16297,BMG_DS062509,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24"
+BMGC_DS16298,BMG_DS062510,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 44
+BMGC_DS16299,BMG_DS062511,OROFACIODIGITAL SYNDROME XV
+BMGC_DS16300,BMG_DS062512,ALAZAMI-YUAN SYNDROME
+BMGC_DS16301,BMG_DS062513,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 56"
+BMGC_DS16302,BMG_DS062514,RETINITIS PIGMENTOSA 76
+BMGC_DS16303,BMG_DS062515,JOUBERT SYNDROME 28
+BMGC_DS16304,BMG_DS062516,JOUBERT SYNDROME 27
+BMGC_DS16305,BMG_DS062517,BARDET-BIEDL SYNDROME 20
+BMGC_DS16306,BMG_DS062518,"EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3"
+BMGC_DS16307,BMG_DS062519,"EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 2"
+BMGC_DS16308,BMG_DS062520,PEELING SKIN SYNDROME 5
+BMGC_DS16309,BMG_DS062521,"MYOPATHY, MYOFIBRILLAR, 7"
+BMGC_DS16310,BMG_DS062522,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 43
+BMGC_DS16311,BMG_DS062523,Martinique crinkled retinal pigment epitheliopathy
+BMGC_DS16312,BMG_DS062524,sessile serrated polyposis cancer syndrome
+BMGC_DS16313,BMG_DS062525,"Tall stature, intellectual disability, renal anomalies syndrome"
+BMGC_DS16314,BMG_DS062526,"developmental and epileptic encephalopathy, 42"
+BMGC_DS16315,BMG_DS062527,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 41
+BMGC_DS16316,BMG_DS062528,SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY
+BMGC_DS16317,BMG_DS062529,FAMILIAL ADENOMATOUS POLYPOSIS 4
+BMGC_DS16318,BMG_DS062530,"GROWTH RETARDATION, IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND HEPATOPATHY"
+BMGC_DS16319,BMG_DS062531,"CILIARY DYSKINESIA, PRIMARY, 35"
+BMGC_DS16320,BMG_DS062532,"CILIARY DYSKINESIA, PRIMARY, 34"
+BMGC_DS16321,BMG_DS062533,"MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS16322,BMG_DS062534,SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY
+BMGC_DS16323,BMG_DS062535,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B"
+BMGC_DS16324,BMG_DS062536,ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2
+BMGC_DS16325,BMG_DS062537,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iaa"
+BMGC_DS16326,BMG_DS062538,"SEIZURES, BENIGN FAMILIAL INFANTILE, 5"
+BMGC_DS16327,BMG_DS062539,"nasopharyngeal carcinoma, susceptibility to, 3"
+BMGC_DS16328,BMG_DS062540,"TOOTH AGENESIS, SELECTIVE, 8"
+BMGC_DS16329,BMG_DS062541,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4"
+BMGC_DS16330,BMG_DS062542,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3"
+BMGC_DS16331,BMG_DS062543,"PORTAL HYPERTENSION, NONCIRRHOTIC, 1"
+BMGC_DS16332,BMG_DS062544,"Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome"
+BMGC_DS16333,BMG_DS062545,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 40
+BMGC_DS16334,BMG_DS062546,MEIER-GORLIN SYNDROME 7
+BMGC_DS16335,BMG_DS062547,OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
+BMGC_DS16336,BMG_DS062548,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 44, WITH MICROCEPHALY"
+BMGC_DS16337,BMG_DS062549,"TUBULOINTERSTITIAL KIDNEY DISEASE, AUTOSOMAL DOMINANT, 5"
+BMGC_DS16338,BMG_DS062550,PERCHING SYNDROME
+BMGC_DS16339,BMG_DS062551,Childhood-onset basal ganglia degeneration syndrome
+BMGC_DS16340,BMG_DS062552,BONE MARROW FAILURE SYNDROME 3
+BMGC_DS16341,BMG_DS062553,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND GRAY SCLERAE
+BMGC_DS16342,BMG_DS062554,HERMANSKY-PUDLAK SYNDROME 10
+BMGC_DS16343,BMG_DS062555,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5"
+BMGC_DS16344,BMG_DS062556,"CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 5"
+BMGC_DS16345,BMG_DS062557,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26"
+BMGC_DS16346,BMG_DS062558,DUANE RETRACTION SYNDROME 3 WITH OR WITHOUT DEAFNESS
+BMGC_DS16347,BMG_DS062559,patent ductus arteriosus 3
+BMGC_DS16348,BMG_DS062560,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 54"
+BMGC_DS16349,BMG_DS062561,"HYPERALDOSTERONISM, FAMILIAL, TYPE IV"
+BMGC_DS16350,BMG_DS062562,"PONTOCEREBELLAR HYPOPLASIA, TYPE 2F"
+BMGC_DS16351,BMG_DS062563,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H"
+BMGC_DS16352,BMG_DS062564,RETINITIS PIGMENTOSA 75
+BMGC_DS16353,BMG_DS062565,"Hydrops, lactic acidosis, sideroblastic anemia, multisystemic failure syndrome"
+BMGC_DS16354,BMG_DS062566,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 38
+BMGC_DS16355,BMG_DS062567,SPINOCEREBELLAR ATAXIA 43
+BMGC_DS16356,BMG_DS062568,"NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE"
+BMGC_DS16357,BMG_DS062569,Hypermanganesemia with dystonia 2
+BMGC_DS16358,BMG_DS062570,"MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION"
+BMGC_DS16359,BMG_DS062571,"CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3"
+BMGC_DS16360,BMG_DS062572,"AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2"
+BMGC_DS16361,BMG_DS062573,POLYCYSTIC LIVER DISEASE 2 WITH OR WITHOUT KIDNEY CYSTS
+BMGC_DS16362,BMG_DS062574,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 37
+BMGC_DS16363,BMG_DS062575,"intellectual disability, autosomal dominant 43"
+BMGC_DS16364,BMG_DS062576,"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART"
+BMGC_DS16365,BMG_DS062577,"intellectual disability, autosomal dominant 42"
+BMGC_DS16366,BMG_DS062578,"DEAFNESS, AUTOSOMAL DOMINANT 70"
+BMGC_DS16367,BMG_DS062579,RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS
+BMGC_DS16368,BMG_DS062580,"TELO2-related intellectual disability, neurodevelopmental disorder"
+BMGC_DS16369,BMG_DS062581,SPERMATOGENIC FAILURE 15
+BMGC_DS16370,BMG_DS062582,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22"
+BMGC_DS16371,BMG_DS062583,PREMATURE OVARIAN FAILURE 12
+BMGC_DS16372,BMG_DS062584,PREMATURE OVARIAN FAILURE 11
+BMGC_DS16373,BMG_DS062585,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 41"
+BMGC_DS16374,BMG_DS062586,"TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE"
+BMGC_DS16375,BMG_DS062587,"AGAMMAGLOBULINEMIA 8A, AUTOSOMAL DOMINANT"
+BMGC_DS16376,BMG_DS062588,"CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION"
+BMGC_DS16377,BMG_DS062589,COFFIN-SIRIS SYNDROME 5
+BMGC_DS16378,BMG_DS062590,THROMBOCYTOPENIA 6
+BMGC_DS16379,BMG_DS062591,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC"
+BMGC_DS16380,BMG_DS062592,"STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2"
+BMGC_DS16381,BMG_DS062593,HEART AND BRAIN MALFORMATION SYNDROME
+BMGC_DS16382,BMG_DS062594,"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPOTONIA, SEIZURES, AND CEREBELLAR ATROPHY"
+BMGC_DS16383,BMG_DS062595,MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME
+BMGC_DS16384,BMG_DS062596,"BLEEDING DISORDER, PLATELET-TYPE, 20"
+BMGC_DS16385,BMG_DS062597,IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4
+BMGC_DS16386,BMG_DS062598,IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3
+BMGC_DS16387,BMG_DS062599,"Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome"
+BMGC_DS16388,BMG_DS062600,"PARKINSON DISEASE 19B, EARLY-ONSET"
+BMGC_DS16389,BMG_DS062601,IMMUNODEFICIENCY 51
+BMGC_DS16390,BMG_DS062602,Witteveen Kolk syndrome
+BMGC_DS16391,BMG_DS062603,"BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS"
+BMGC_DS16392,BMG_DS062604,CATARACT 47
+BMGC_DS16393,BMG_DS062605,BRACHYDACTYLY-SYNDACTYLY-OLIGODACTYLY SYNDROME
+BMGC_DS16394,BMG_DS062606,"STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 1"
+BMGC_DS16395,BMG_DS062607,ANTERIOR SEGMENT DYSGENESIS 5
+BMGC_DS16396,BMG_DS062608,"MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS"
+BMGC_DS16397,BMG_DS062609,MEESTER-LOEYS SYNDROME
+BMGC_DS16398,BMG_DS062610,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BAIN TYPE"
+BMGC_DS16399,BMG_DS062611,"VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF, X-LINKED"
+BMGC_DS16400,BMG_DS062612,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 105"
+BMGC_DS16401,BMG_DS062613,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 104"
+BMGC_DS16402,BMG_DS062614,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 103"
+BMGC_DS16403,BMG_DS062615,IMMUNODEFICIENCY 47
+BMGC_DS16404,BMG_DS062616,"BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT"
+BMGC_DS16405,BMG_DS062617,LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY
+BMGC_DS16406,BMG_DS062618,"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, AND MILD PALMOPLANTAR KERATODERMA WITH OR WITHOUT WOOLLY HAIR"
+BMGC_DS16407,BMG_DS062619,"antisocial behavior, susceptibility to"
+BMGC_DS16408,BMG_DS062620,Dias-Logan syndrome
+BMGC_DS16409,BMG_DS062621,"ALACRIMA, CONGENITAL, AUTOSOMAL DOMINANT"
+BMGC_DS16410,BMG_DS062622,"SANDHOFF DISEASE, CHRONIC"
+BMGC_DS16411,BMG_DS062627,DUANE RETRACTION SYNDROME 3
+BMGC_DS16412,BMG_DS062636,"BETA-HEXOSAMINIDASE A, PSEUDODEFICIENCY OF"
+BMGC_DS16413,BMG_DS062637,"GM2-GANGLIOSIDOSIS, ADULT-ONSET"
+BMGC_DS16414,BMG_DS062647,"ANTERIOR SEGMENT DYSGENESIS 1, MULTIPLE SUBTYPES"
+BMGC_DS16415,BMG_DS062657,GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE
+BMGC_DS16416,BMG_DS062663,"BETA-THALASSEMIA, ASHKENAZI JEWISH TYPE"
+BMGC_DS16417,BMG_DS062664,"BETA-THALASSEMIA INTERMEDIA, DOMINANT"
+BMGC_DS16418,BMG_DS062668,"CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL"
+BMGC_DS16419,BMG_DS062669,"CHROMOSOME 11p13 DELETION SYNDROME, DISTAL"
+BMGC_DS16420,BMG_DS062670,"CHROMOSOME 19q13.11 DELETION SYNDROME, DISTAL"
+BMGC_DS16421,BMG_DS062671,CHROMOSOME Xq25 DUPLICATION SYNDROME
+BMGC_DS16422,BMG_DS062677,Nocturnal frontal lobe epilepsy
+BMGC_DS16423,BMG_DS062701,brachydactyly type E
+BMGC_DS16424,BMG_DS062793,"Kenny-Caffey syndrome, type 2"
+BMGC_DS16425,BMG_DS062794,partial lipodystrophy
+BMGC_DS16426,BMG_DS062796,Entamoeba histolytica Infection
+BMGC_DS16427,BMG_DS062799,Writer's Cramp
+BMGC_DS16428,BMG_DS062800,Fibrinogen Deficiency
+BMGC_DS16429,BMG_DS062802,eye disorder
+BMGC_DS16430,BMG_DS062806,Cystinosis
+BMGC_DS16431,BMG_DS062807,Absence Seizures
+BMGC_DS16432,BMG_DS062811,Primary Hypothyroidism
+BMGC_DS16433,BMG_DS062812,Diverticular Diseases
+BMGC_DS16434,BMG_DS062813,Simpson-Golabi-Behmel syndrome
+BMGC_DS16435,BMG_DS062816,thyroid gland disorder
+BMGC_DS16436,BMG_DS062817,Epileptic Seizures
+BMGC_DS16437,BMG_DS062819,Polynesian Bronchiectasis
+BMGC_DS16438,BMG_DS062820,Niacin deficiency
+BMGC_DS16439,BMG_DS062821,"Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome"
+BMGC_DS16440,BMG_DS062823,COLE-CARPENTER SYNDROME 1
+BMGC_DS16441,BMG_DS062824,Adolescent Obesity
+BMGC_DS16442,BMG_DS062826,Congenital disorder of glycosylation type 1q
+BMGC_DS16443,BMG_DS062827,Congenital disorder of glycosylation type 1s
+BMGC_DS16444,BMG_DS062829,Factor V deficiency
+BMGC_DS16445,BMG_DS062830,Juvenile Absence Epilepsy
+BMGC_DS16446,BMG_DS062831,growth hormone insensitivity syndrome
+BMGC_DS16447,BMG_DS062840,BARDET-BIEDL SYNDROME 21
+BMGC_DS16448,BMG_DS062841,cleft lip
+BMGC_DS16449,BMG_DS062857,Hyperandrogenism due to cortisone reductase deficiency
+BMGC_DS16450,BMG_DS062860,acute myeloid leukemia with CBFA2T3-GLIS2 fusion
+BMGC_DS16451,BMG_DS062864,Autosomal recessive infantile hypercalcemia
+BMGC_DS16452,BMG_DS062871,early T cell progenitor acute lymphoblastic leukemia
+BMGC_DS16453,BMG_DS062883,rosette-forming glioneuronal tumor of fourth ventricule
+BMGC_DS16454,BMG_DS062888,atrial septal aneurysm
+BMGC_DS16455,BMG_DS062893,"CILIARY DYSKINESIA, PRIMARY, 36, X-LINKED"
+BMGC_DS16456,BMG_DS062894,"intellectual disability, X-linked 106"
+BMGC_DS16457,BMG_DS062895,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 35"
+BMGC_DS16458,BMG_DS062901,NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1
+BMGC_DS16459,BMG_DS062903,brain malformations with or without urinary tract defects
+BMGC_DS16460,BMG_DS062904,"MYASTHENIC SYNDROME, CONGENITAL, 22"
+BMGC_DS16461,BMG_DS062906,CONGENITAL MYOPATHY 24
+BMGC_DS16462,BMG_DS062907,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 51
+BMGC_DS16463,BMG_DS062908,CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2
+BMGC_DS16464,BMG_DS062909,HYPERPARATHYROIDISM 4
+BMGC_DS16465,BMG_DS062910,"aortic aneurysm, familial thoracic 11, susceptibility to"
+BMGC_DS16466,BMG_DS062911,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 52
+BMGC_DS16467,BMG_DS062912,"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER"
+BMGC_DS16468,BMG_DS062913,CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA
+BMGC_DS16469,BMG_DS062914,PEROXISOME BIOGENESIS DISORDER 10B
+BMGC_DS16470,BMG_DS062915,"AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 2"
+BMGC_DS16471,BMG_DS062916,"HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT"
+BMGC_DS16472,BMG_DS062917,AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS
+BMGC_DS16473,BMG_DS062918,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 53
+BMGC_DS16474,BMG_DS062919,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 54
+BMGC_DS16475,BMG_DS062920,"ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE"
+BMGC_DS16476,BMG_DS062921,"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION"
+BMGC_DS16477,BMG_DS062922,"SCLEROSING CHOLANGITIS, NEONATAL"
+BMGC_DS16478,BMG_DS062923,COG2-related congenital disorder of glycosylation
+BMGC_DS16479,BMG_DS062924,ANAUXETIC DYSPLASIA 2
+BMGC_DS16480,BMG_DS062925,PSEUDO-TORCH SYNDROME 2
+BMGC_DS16481,BMG_DS062926,"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC"
+BMGC_DS16482,BMG_DS062927,"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID"
+BMGC_DS16483,BMG_DS062928,"MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY"
+BMGC_DS16484,BMG_DS062929,SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY
+BMGC_DS16485,BMG_DS062930,DIAMOND-BLACKFAN ANEMIA 16
+BMGC_DS16486,BMG_DS062931,DIAMOND-BLACKFAN ANEMIA 17
+BMGC_DS16487,BMG_DS062932,"BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY"
+BMGC_DS16488,BMG_DS062933,IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES
+BMGC_DS16489,BMG_DS062935,"intellectual disability, autosomal recessive 60"
+BMGC_DS16490,BMG_DS062936,RETINITIS PIGMENTOSA 78
+BMGC_DS16491,BMG_DS062937,LOPES-MACIEL-RODAN SYNDROME
+BMGC_DS16492,BMG_DS062938,CRANIOSYNOSTOSIS 7
+BMGC_DS16493,BMG_DS062939,"THROMBOCYTOPENIA, ANEMIA, AND MYELOFIBROSIS"
+BMGC_DS16494,BMG_DS062940,PREMATURE OVARIAN FAILURE 13
+BMGC_DS16495,BMG_DS062941,"BLEEDING DISORDER, PLATELET-TYPE, 21"
+BMGC_DS16496,BMG_DS062942,JANSEN-DE VRIES SYNDROME
+BMGC_DS16497,BMG_DS062943,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES"
+BMGC_DS16498,BMG_DS062944,RETINITIS PIGMENTOSA 79
+BMGC_DS16499,BMG_DS062945,TOWNES-BROCKS SYNDROME 2
+BMGC_DS16500,BMG_DS062946,"ARTHROGRYPOSIS MULTIPLEX CONGENITA 1, NEUROGENIC, WITH MYELIN DEFECT"
+BMGC_DS16501,BMG_DS062947,SPECIFIC GRANULE DEFICIENCY 2
+BMGC_DS16502,BMG_DS062948,STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME
+BMGC_DS16503,BMG_DS062949,"46,XX sex reversal 4"
+BMGC_DS16504,BMG_DS062950,PRUNE1-related neurological syndrome
+BMGC_DS16505,BMG_DS062951,NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS
+BMGC_DS16506,BMG_DS062952,NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2
+BMGC_DS16507,BMG_DS062953,IMMUNODEFICIENCY 52
+BMGC_DS16508,BMG_DS062955,STANKIEWICZ-ISIDOR SYNDROME
+BMGC_DS16509,BMG_DS062956,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS"
+BMGC_DS16510,BMG_DS062957,"MICROCEPHALY 18, PRIMARY, AUTOSOMAL DOMINANT"
+BMGC_DS16511,BMG_DS062958,NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS
+BMGC_DS16512,BMG_DS062959,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 2
+BMGC_DS16513,BMG_DS062960,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 3
+BMGC_DS16514,BMG_DS062961,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 4
+BMGC_DS16515,BMG_DS062962,PLAA-associated neurodevelopmental disorder
+BMGC_DS16516,BMG_DS062963,INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES
+BMGC_DS16517,BMG_DS062964,"Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1-4 mutation"
+BMGC_DS16518,BMG_DS062965,"GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS 2, WITH IMPAIRED INTELLECTUAL DEVELOPMENT"
+BMGC_DS16519,BMG_DS062967,RETINAL DYSTROPHY WITH OR WITHOUT MACULAR STAPHYLOMA
+BMGC_DS16520,BMG_DS062968,Gabriele-de Vries syndrome
+BMGC_DS16521,BMG_DS062969,NKX6-2-related autosomal recessive hypomyelinating leukodystrophy
+BMGC_DS16522,BMG_DS062970,COHEN-GIBSON SYNDROME
+BMGC_DS16523,BMG_DS062971,MEIER-GORLIN SYNDROME 8
+BMGC_DS16524,BMG_DS062972,PERRAULT SYNDROME 6
+BMGC_DS16525,BMG_DS062975,"HYPERLIPOPROTEINEMIA, TYPE III, DUE TO APOE2"
+BMGC_DS16526,BMG_DS062976,"ADRENAL INSUFFICIENCY, NR5A1-RELATED"
+BMGC_DS16527,BMG_DS063000,Epileptic Syndromes
+BMGC_DS16528,BMG_DS063011,Xp21 Contiguous Gene Deletion Syndrome
+BMGC_DS16529,BMG_DS063016,Diverticular Bleeding
+BMGC_DS16530,BMG_DS063019,Mycoplasma ovipneumoniae Infection
+BMGC_DS16531,BMG_DS063020,Mycoplasma dispar Infection
+BMGC_DS16532,BMG_DS063025,Generalized Absence Seizures
+BMGC_DS16533,BMG_DS063026,Trichophyton mentagrophytes Infection
+BMGC_DS16534,BMG_DS063027,HIV Coinfection
+BMGC_DS16535,BMG_DS063036,"Chemical and Drug Induced Liver Injury, Chronic"
+BMGC_DS16536,BMG_DS063037,"Chemical-Induced Liver Injury, Chronic"
+BMGC_DS16537,BMG_DS063041,isolated bone marrow mastocytosis
+BMGC_DS16538,BMG_DS063044,Senile systemic amyloidosis (SSA)
+BMGC_DS16539,BMG_DS063137,Celiac gluten-sensitive enteropathy
+BMGC_DS16540,BMG_DS063276,non-small cell squamous lung carcinoma
+BMGC_DS16541,BMG_DS063279,Endocrine-cerebro-osteodysplasia syndrome
+BMGC_DS16542,BMG_DS063280,FADD-related immunodeficiency
+BMGC_DS16543,BMG_DS063281,Familial acute necrotizing encephalopathy
+BMGC_DS16544,BMG_DS063285,Mendelian susceptibility to mycobacterial disease due to complete ISG15 deficiency
+BMGC_DS16545,BMG_DS063286,Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency
+BMGC_DS16546,BMG_DS063287,Mendelian susceptibility to mycobacterial disease due to partial STAT1 deficiency
+BMGC_DS16547,BMG_DS063292,Microcephalic osteodysplastic dysplasia Saul Wilson type
+BMGC_DS16548,BMG_DS063295,Muscular dystrophy Selcen type
+BMGC_DS16549,BMG_DS063296,Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus
+BMGC_DS16550,BMG_DS063308,Non-progressive cerebellar ataxia with intellectual disability
+BMGC_DS16551,BMG_DS063309,Polyvalvular heart disease syndrome
+BMGC_DS16552,BMG_DS063311,"Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome"
+BMGC_DS16553,BMG_DS063315,NK-cell enteropathy
+BMGC_DS16554,BMG_DS063316,Peripheral neuropathy with sensorineural hearing impairment syndrome
+BMGC_DS16555,BMG_DS063321,Terminal osseous dysplasia and pigmentary defect syndrome
+BMGC_DS16556,BMG_DS063335,Severe generalized recessive dystrophic epidermolysis bullosa
+BMGC_DS16557,BMG_DS063358,Idiopathic ventricular fibrillation not Brugada type
+BMGC_DS16558,BMG_DS063368,Sensorineural deafness with dilated cardiomyopathy syndrome
+BMGC_DS16559,BMG_DS063389,"Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome"
+BMGC_DS16560,BMG_DS063390,Myopathy due to calsequestrin and SERCA1 protein overload
+BMGC_DS16561,BMG_DS063393,Microcephalic primordial dwarfism due to ZNF335 deficiency
+BMGC_DS16562,BMG_DS063395,"Metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome"
+BMGC_DS16563,BMG_DS063396,McLeod neuroacanthocytosis syndrome
+BMGC_DS16564,BMG_DS063398,Laron syndrome with immunodeficiency
+BMGC_DS16565,BMG_DS063422,Congenital ichthyosis with hypotrichosis syndrome
+BMGC_DS16566,BMG_DS063423,"Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome"
+BMGC_DS16567,BMG_DS063428,Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
+BMGC_DS16568,BMG_DS063429,"Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome"
+BMGC_DS16569,BMG_DS063432,Hereditary combined deficiency of vitamin K-dependent clotting factors
+BMGC_DS16570,BMG_DS063433,Hepatic veno-occlusive disease with immunodeficiency syndrome
+BMGC_DS16571,BMG_DS063442,Pneumonia caused by Chlamydia pneumoniae
+BMGC_DS16572,BMG_DS063456,Frontonasal dysplasia with alopecia and genital anomaly syndrome
+BMGC_DS16573,BMG_DS063461,"46,XY partial gonadal dysgenesis"
+BMGC_DS16574,BMG_DS063463,Muscle and heart glycogen synthase deficiency
+BMGC_DS16575,BMG_DS063464,Hepatic glycogen synthase deficiency
+BMGC_DS16576,BMG_DS063467,Infantile osteopetrosis with neuroaxonal dysplasia syndrome
+BMGC_DS16577,BMG_DS063484,Craniometadiaphyseal dysplasia wormian bone type
+BMGC_DS16578,BMG_DS063486,Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
+BMGC_DS16579,BMG_DS063516,Combined immunodeficiency due to CD3gamma deficiency
+BMGC_DS16580,BMG_DS063518,"Atrial septal defect, atrioventricular conduction defect syndrome"
+BMGC_DS16581,BMG_DS063519,Atypical juvenile parkinsonism
+BMGC_DS16582,BMG_DS063521,Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
+BMGC_DS16583,BMG_DS063523,Omodysplasia
+BMGC_DS16584,BMG_DS063527,3-hydroxy-3-methylglutaryl-coenzyme A synthase deficiency
+BMGC_DS16585,BMG_DS063529,Combined immunodeficiency due to partial RAG1 deficiency
+BMGC_DS16586,BMG_DS063530,Defect of purinergic receptor p2y G protein-coupled 12
+BMGC_DS16587,BMG_DS063532,"X-linked spasticity, intellectual disability, epilepsy syndrome"
+BMGC_DS16588,BMG_DS063540,Puberty disorder due to estrogen resistance
+BMGC_DS16589,BMG_DS063553,acute myeloid leukemia with t(8;16)(p11;p13) translocation
+BMGC_DS16590,BMG_DS063554,Autosomal dominant striatal neurodegeneration
+BMGC_DS16591,BMG_DS063566,Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type
+BMGC_DS16592,BMG_DS063576,Congenital muscular dystrophy Paradas type
+BMGC_DS16593,BMG_DS063577,Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency
+BMGC_DS16594,BMG_DS063578,Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency
+BMGC_DS16595,BMG_DS063579,Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
+BMGC_DS16596,BMG_DS063580,Severe congenital hypochromic anemia with ringed sideroblasts
+BMGC_DS16597,BMG_DS063581,Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
+BMGC_DS16598,BMG_DS063586,Bathing suit ichthyosis
+BMGC_DS16599,BMG_DS063593,Butterfly-shaped pigmentary macular dystrophy
+BMGC_DS16600,BMG_DS063595,Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization
+BMGC_DS16601,BMG_DS063647,Autosomal recessive limb girdle muscular dystrophy type 2Y
+BMGC_DS16602,BMG_DS063654,Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
+BMGC_DS16603,BMG_DS063662,Cannabis hyperemesis syndrome co-occurrent and due to cannabis abuse
+BMGC_DS16604,BMG_DS063663,Cannabis hyperemesis syndrome co-occurrent and due to cannabis dependence
+BMGC_DS16605,BMG_DS063668,Autosomal dominant tubulointerstitial kidney disease
+BMGC_DS16606,BMG_DS063672,CAMOS syndrome
+BMGC_DS16607,BMG_DS063675,Hereditary hypercarotenemia and vitamin A deficiency
+BMGC_DS16608,BMG_DS063677,X-linked diffuse leiomyomatosis with Alport syndrome
+BMGC_DS16609,BMG_DS063717,Autosomal recessive limb girdle muscular dystrophy type 2P
+BMGC_DS16610,BMG_DS063719,Spastic paraplegia with Paget disease of bone syndrome
+BMGC_DS16611,BMG_DS063723,"Central nervous system calcification, deafness, tubular acidosis, anemia syndrome"
+BMGC_DS16612,BMG_DS063728,Epileptic encephalopathy with global cerebral demyelination
+BMGC_DS16613,BMG_DS063733,X-linked intellectual disability Nascimento type
+BMGC_DS16614,BMG_DS063740,"X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency"
+BMGC_DS16615,BMG_DS063747,Coenzyme A synthase protein associated neurodegeneration
+BMGC_DS16616,BMG_DS063751,Autosomal recessive limb girdle muscular dystrophy type 2S
+BMGC_DS16617,BMG_DS063752,Autosomal recessive limb girdle muscular dystrophy type 2T
+BMGC_DS16618,BMG_DS063759,"Autism spectrum disorder, epilepsy, arthrogryposis syndrome"
+BMGC_DS16619,BMG_DS063766,Acral dystrophic epidermolysis bullosa
+BMGC_DS16620,BMG_DS063814,Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency
+BMGC_DS16621,BMG_DS063815,"Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome"
+BMGC_DS16622,BMG_DS063817,clear cell papillary renal cell carcinoma
+BMGC_DS16623,BMG_DS063820,Spinocerebellar ataxia type 40
+BMGC_DS16624,BMG_DS063821,Spinocerebellar ataxia type 38 (disorder)
+BMGC_DS16625,BMG_DS063822,Wolfram-like syndrome
+BMGC_DS16626,BMG_DS063825,isolated congenital megalocornea
+BMGC_DS16627,BMG_DS063827,Distal 22q11.2 microdeletion syndrome
+BMGC_DS16628,BMG_DS063828,12q15q21.1 microdeletion syndrome
+BMGC_DS16629,BMG_DS063830,MIT family translocation renal cell carcinoma
+BMGC_DS16630,BMG_DS063883,Early-onset Lafora body disease
+BMGC_DS16631,BMG_DS063924,Epilepsy of infancy with migrating focal seizures
+BMGC_DS16632,BMG_DS063944,Noninfectious panuveitis
+BMGC_DS16633,BMG_DS063949,Joubert syndrome with Jeune asphyxiating thoracic dystrophy
+BMGC_DS16634,BMG_DS063951,Prion protein systemic amyloidosis
+BMGC_DS16635,BMG_DS063952,Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency
+BMGC_DS16636,BMG_DS063954,Carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency
+BMGC_DS16637,BMG_DS063955,"Leukoencephalopathy, dystonia, motor neuropathy syndrome"
+BMGC_DS16638,BMG_DS063956,"Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome"
+BMGC_DS16639,BMG_DS063958,Ehlers-Danlos and osteogenesis imperfecta syndrome
+BMGC_DS16640,BMG_DS063964,Distal myopathy with posterior leg and anterior hand involvement
+BMGC_DS16641,BMG_DS063967,17q12 microdeletion syndrome
+BMGC_DS16642,BMG_DS063969,Distal 16p11.2 microdeletion syndrome
+BMGC_DS16643,BMG_DS063971,acute myeloid leukemia with t(6;9)(p23;q34)
+BMGC_DS16644,BMG_DS063972,Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency
+BMGC_DS16645,BMG_DS063973,Combined oxidative phosphorylation defect type 8
+BMGC_DS16646,BMG_DS064121,erythroleukemia
+BMGC_DS16647,BMG_DS064123,Otospondylomegaepiphyseal dysplasia
+BMGC_DS16648,BMG_DS064125,basal ganglia disorder
+BMGC_DS16649,BMG_DS064126,extrahepatic biliary atresia
+BMGC_DS16650,BMG_DS064127,Juvenile polyarthritis
+BMGC_DS16651,BMG_DS064129,ACROMEGALY DUE TO PITUITARY ADENOMA 1
+BMGC_DS16652,BMG_DS064134,SPINOCEREBELLAR ATAXIA 44
+BMGC_DS16653,BMG_DS064135,"FANCONI ANEMIA, COMPLEMENTATION GROUP W"
+BMGC_DS16654,BMG_DS064136,AUDITORY NEUROPATHY AND OPTIC ATROPHY
+BMGC_DS16655,BMG_DS064137,"DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION"
+BMGC_DS16656,BMG_DS064140,HELIX SYNDROME
+BMGC_DS16657,BMG_DS064151,high grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement
+BMGC_DS16658,BMG_DS064158,breast implant-associated anaplastic large cell lymphoma
+BMGC_DS16659,BMG_DS064166,growth hormone secreting pituitary adenoma 1
+BMGC_DS16660,BMG_DS064168,MARSILI SYNDROME
+BMGC_DS16661,BMG_DS064169,"SYRINGOMYELIA, NONCOMMUNICATING ISOLATED"
+BMGC_DS16662,BMG_DS064170,"COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY"
+BMGC_DS16663,BMG_DS064171,DIENCEPHALIC-MESENCEPHALIC JUNCTION DYSPLASIA SYNDROME 1
+BMGC_DS16664,BMG_DS064173,"GALLOWAY-MOWAT SYNDROME 2, X-LINKED"
+BMGC_DS16665,BMG_DS064174,"intellectual disability, X-linked, syndromic, Houge type"
+BMGC_DS16666,BMG_DS064175,"MYOPIA 26, X-LINKED, FEMALE-LIMITED"
+BMGC_DS16667,BMG_DS064179,JOUBERT SYNDROME 34
+BMGC_DS16668,BMG_DS064182,"pituitary adenoma 5, multiple types"
+BMGC_DS16669,BMG_DS064184,MECKEL SYNDROME 13
+BMGC_DS16670,BMG_DS064185,JOUBERT SYNDROME 29
+BMGC_DS16671,BMG_DS064186,OROFACIODIGITAL SYNDROME XVI
+BMGC_DS16672,BMG_DS064187,"ichthyosis, congenital, autosomal recessive 14"
+BMGC_DS16673,BMG_DS064188,EXUDATIVE VITREORETINOPATHY 7
+BMGC_DS16674,BMG_DS064189,"ichthyosis, congenital, autosomal recessive 13"
+BMGC_DS16675,BMG_DS064190,SPERMATOGENIC FAILURE 18
+BMGC_DS16676,BMG_DS064191,"CILIARY DYSKINESIA, PRIMARY, 37"
+BMGC_DS16677,BMG_DS064192,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25"
+BMGC_DS16678,BMG_DS064193,IMMUNODEFICIENCY 53
+BMGC_DS16679,BMG_DS064194,SPERMATOGENIC FAILURE 19
+BMGC_DS16680,BMG_DS064195,SPERMATOGENIC FAILURE 20
+BMGC_DS16681,BMG_DS064196,BIRK-LANDAU-PEREZ SYNDROME
+BMGC_DS16682,BMG_DS064197,MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 3
+BMGC_DS16683,BMG_DS064198,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 55
+BMGC_DS16684,BMG_DS064199,"intellectual disability, autosomal dominant 45"
+BMGC_DS16685,BMG_DS064200,"intellectual disability, autosomal dominant 46"
+BMGC_DS16686,BMG_DS064201,CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME
+BMGC_DS16687,BMG_DS064202,"MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES"
+BMGC_DS16688,BMG_DS064203,"DEAFNESS, AUTOSOMAL DOMINANT 71"
+BMGC_DS16689,BMG_DS064204,"DEAFNESS, AUTOSOMAL DOMINANT 72"
+BMGC_DS16690,BMG_DS064205,"AMELOGENESIS IMPERFECTA, TYPE IIIB"
+BMGC_DS16691,BMG_DS064206,"NEPHROTIC SYNDROME, TYPE 15"
+BMGC_DS16692,BMG_DS064207,POLYCYSTIC KIDNEY DISEASE 5
+BMGC_DS16693,BMG_DS064208,Multiple mitochondrial dysfunctions syndrome type 5
+BMGC_DS16694,BMG_DS064209,SKRABAN-DEARDORFF SYNDROME
+BMGC_DS16695,BMG_DS064210,JOUBERT SYNDROME 30
+BMGC_DS16696,BMG_DS064211,"FIBROMATOSIS, GINGIVAL, 5"
+BMGC_DS16697,BMG_DS064212,schizophrenia 19
+BMGC_DS16698,BMG_DS064213,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26"
+BMGC_DS16699,BMG_DS064214,"intellectual disability, autosomal dominant 47"
+BMGC_DS16700,BMG_DS064215,"DEAFNESS, AUTOSOMAL RECESSIVE 106"
+BMGC_DS16701,BMG_DS064216,IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS
+BMGC_DS16702,BMG_DS064217,"DEAFNESS, 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"
+BMGC_DS16704,BMG_DS064219,"polydactyly, postaxial, type a7"
+BMGC_DS16705,BMG_DS064220,"CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES"
+BMGC_DS16706,BMG_DS064221,SPERMATOGENIC FAILURE 21
+BMGC_DS16707,BMG_DS064222,"DEAFNESS, AUTOSOMAL RECESSIVE 108"
+BMGC_DS16708,BMG_DS064223,"VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1"
+BMGC_DS16709,BMG_DS064224,"VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2"
+BMGC_DS16710,BMG_DS064225,"Severe myopia, generalized joint laxity, short stature syndrome"
+BMGC_DS16711,BMG_DS064226,"DEAFNESS, AUTOSOMAL DOMINANT 73"
+BMGC_DS16712,BMG_DS064227,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32
+BMGC_DS16713,BMG_DS064228,combined oxidative phosphorylation deficiency
+BMGC_DS16714,BMG_DS064229,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 56
+BMGC_DS16715,BMG_DS064230,FRASER SYNDROME 2
+BMGC_DS16716,BMG_DS064231,FRASER SYNDROME 3
+BMGC_DS16717,BMG_DS064232,"ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES"
+BMGC_DS16718,BMG_DS064233,"NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY"
+BMGC_DS16719,BMG_DS064234,"Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome"
+BMGC_DS16720,BMG_DS064235,BLEPHAROCHEILODONTIC SYNDROME 2
+BMGC_DS16721,BMG_DS064236,"Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome"
+BMGC_DS16722,BMG_DS064237,"pituitary adenoma 3, multiple types"
+BMGC_DS16723,BMG_DS064238,OVARIAN DYSGENESIS 5
+BMGC_DS16724,BMG_DS064239,AL KAISSI SYNDROME
+BMGC_DS16725,BMG_DS064240,"pontocerebellar hypoplasia, type 11"
+BMGC_DS16726,BMG_DS064241,3-methylglutaconic aciduria type 9
+BMGC_DS16727,BMG_DS064242,SPERMATOGENIC FAILURE 22
+BMGC_DS16728,BMG_DS064243,SPERMATOGENIC FAILURE 23
+BMGC_DS16729,BMG_DS064244,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ATAXIA, AND SEIZURES"
+BMGC_DS16730,BMG_DS064245,WARS2-related combined oxidative phosphorylation defect
+BMGC_DS16731,BMG_DS064246,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 91
+BMGC_DS16732,BMG_DS064247,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 3
+BMGC_DS16733,BMG_DS064248,combined oxidative phosphorylation deficiency 33
+BMGC_DS16734,BMG_DS064249,IMMUNODEFICIENCY 71 WITH INFLAMMATORY DISEASE AND CONGENITAL THROMBOCYTOPENIA
+BMGC_DS16735,BMG_DS064250,"epiphyseal dysplasia, multiple, 7"
+BMGC_DS16736,BMG_DS064253,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 9"
+BMGC_DS16737,BMG_DS064254,GALLOWAY-MOWAT SYNDROME 3
+BMGC_DS16738,BMG_DS064255,GALLOWAY-MOWAT SYNDROME 4
+BMGC_DS16739,BMG_DS064256,GALLOWAY-MOWAT SYNDROME 5
+BMGC_DS16740,BMG_DS064257,"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION"
+BMGC_DS16741,BMG_DS064258,oocyte maturation defect 4
+BMGC_DS16742,BMG_DS064259,"IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA"
+BMGC_DS16743,BMG_DS064260,SWEENEY-COX SYNDROME
+BMGC_DS16744,BMG_DS064261,"intellectual disability, autosomal dominant 48"
+BMGC_DS16745,BMG_DS064262,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES
+BMGC_DS16746,BMG_DS064263,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 5
+BMGC_DS16747,BMG_DS064264,JOUBERT SYNDROME 32
+BMGC_DS16748,BMG_DS064265,"MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION"
+BMGC_DS16749,BMG_DS064266,JOUBERT SYNDROME 31
+BMGC_DS16750,BMG_DS064267,Alkaline ceramidase 3 deficiency
+BMGC_DS16751,BMG_DS064268,"SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES"
+BMGC_DS16752,BMG_DS064270,"IMMUNODEFICIENCY, COMMON VARIABLE, 14"
+BMGC_DS16753,BMG_DS064271,JOUBERT SYNDROME 33
+BMGC_DS16754,BMG_DS064272,KLEEFSTRA SYNDROME 2
+BMGC_DS16755,BMG_DS064273,Spinocerebellar ataxia type 45
+BMGC_DS16756,BMG_DS064274,Spinocerebellar ataxia type 46
+BMGC_DS16757,BMG_DS064275,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 57
+BMGC_DS16758,BMG_DS064276,"intellectual disability, autosomal recessive 61"
+BMGC_DS16759,BMG_DS064277,COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA
+BMGC_DS16760,BMG_DS064278,RETINITIS PIGMENTOSA 80
+BMGC_DS16761,BMG_DS064279,"NEPHROTIC SYNDROME, TYPE 16"
+BMGC_DS16762,BMG_DS064280,"intellectual disability, autosomal dominant 50"
+BMGC_DS16763,BMG_DS064281,"intellectual disability, autosomal dominant 51"
+BMGC_DS16764,BMG_DS064282,"intellectual disability, autosomal dominant 52"
+BMGC_DS16765,BMG_DS064283,"intellectual disability, autosomal dominant 53"
+BMGC_DS16766,BMG_DS064284,"intellectual disability, autosomal dominant 54"
+BMGC_DS16767,BMG_DS064285,"MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS16768,BMG_DS064286,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY"
+BMGC_DS16769,BMG_DS064287,neurodevelopmental disorder with severe motor impairment and absent language
+BMGC_DS16770,BMG_DS064288,renal hypodysplasia/aplasia 3
+BMGC_DS16771,BMG_DS064289,"NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER"
+BMGC_DS16772,BMG_DS064290,COFFIN-SIRIS SYNDROME 6
+BMGC_DS16773,BMG_DS064291,geleophysic dysplasia 3
+BMGC_DS16774,BMG_DS064292,"Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome"
+BMGC_DS16775,BMG_DS064293,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 16
+BMGC_DS16776,BMG_DS064294,GLUCOCORTICOID DEFICIENCY 5
+BMGC_DS16777,BMG_DS064299,"SHORT STATURE AND ADVANCED BONE AGE, WITH EARLY-ONSET OSTEOARTHRITIS"
+BMGC_DS16778,BMG_DS064302,RENI SYNDROME
+BMGC_DS16779,BMG_DS064305,POLYCYSTIC KIDNEY DISEASE 4
+BMGC_DS16780,BMG_DS064510,Disorder of neutrophil chemotaxis
+BMGC_DS16781,BMG_DS064519,Chronic viral hepatitis D
+BMGC_DS16782,BMG_DS064618,Narcolepsy type 1
+BMGC_DS16783,BMG_DS064824,Chronic Primary Pain
+BMGC_DS16784,BMG_DS064898,Hemiparkinsonism hemiatrophy syndrome
+BMGC_DS16785,BMG_DS064942,myeloid neoplasm associated with PDGFRA rearrangement
+BMGC_DS16786,BMG_DS064976,Congenital Zika Syndrome
+BMGC_DS16787,BMG_DS065013,congenital non-communicating hydrocephalus
+BMGC_DS16788,BMG_DS065225,Seckel syndrome 1
+BMGC_DS16789,BMG_DS065226,"ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1"
+BMGC_DS16790,BMG_DS065227,NEU-LAXOVA SYNDROME 1
+BMGC_DS16791,BMG_DS065228,"Schwartz-Jampel Syndrome, Type 1"
+BMGC_DS16792,BMG_DS065229,FRASER SYNDROME 1
+BMGC_DS16793,BMG_DS065230,TOWNES-BROCKS SYNDROME 1
+BMGC_DS16794,BMG_DS065231,Adams-Oliver syndrome 1
+BMGC_DS16795,BMG_DS065232,SCLEROSTEOSIS 1
+BMGC_DS16796,BMG_DS065233,"LEOPARD Syndrome, 1"
+BMGC_DS16797,BMG_DS065234,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1
+BMGC_DS16798,BMG_DS065235,bifid uvula
+BMGC_DS16799,BMG_DS065236,situs inversus
+BMGC_DS16800,BMG_DS065238,"Hypophosphatemic Rickets, Autosomal Recessive, 1"
+BMGC_DS16801,BMG_DS065239,"Hyperuricemic Nephropathy, Familial Juvenile 1"
+BMGC_DS16802,BMG_DS065242,"EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1"
+BMGC_DS16803,BMG_DS065243,"Amyloid Polyneuropathy, Iowa Type"
+BMGC_DS16804,BMG_DS065244,"AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1"
+BMGC_DS16805,BMG_DS065245,HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 1
+BMGC_DS16806,BMG_DS065246,FANCONI RENOTUBULAR SYNDROME 1
+BMGC_DS16807,BMG_DS065247,Oculocutaneous albinism type 1A
+BMGC_DS16808,BMG_DS065248,Methylcrotonyl-CoA carboxylase deficiency
+BMGC_DS16809,BMG_DS065249,Paroxysmal Nonkinesigenic Dyskinesia 1
+BMGC_DS16810,BMG_DS065250,Dominant hereditary optic atrophy
+BMGC_DS16811,BMG_DS065251,Jervell And Lange-Nielsen Syndrome 1
+BMGC_DS16812,BMG_DS065252,CARPENTER SYNDROME 1
+BMGC_DS16813,BMG_DS065253,X-linked sideroblastic anemia
+BMGC_DS16814,BMG_DS065254,DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA
+BMGC_DS16815,BMG_DS065255,"Hemophagocytic Lymphohistiocytosis, Familial, 1"
+BMGC_DS16816,BMG_DS065256,Chilblain lupus erythematosus
+BMGC_DS16817,BMG_DS065257,Abducens Nerve Palsy
+BMGC_DS16818,BMG_DS065258,Focal segmental glomerulosclerosis 1
+BMGC_DS16819,BMG_DS065260,"EPILEPSY, HOT WATER, 1"
+BMGC_DS16820,BMG_DS065261,X-linked hereditary motor and sensory neuropathy
+BMGC_DS16821,BMG_DS065262,"CEREBELLAR ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSEQUILIBRIUM SYNDROME 1"
+BMGC_DS16822,BMG_DS065263,SPECIFIC GRANULE DEFICIENCY 1
+BMGC_DS16823,BMG_DS065264,IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1
+BMGC_DS16824,BMG_DS065265,"Fibromatosis, Gingival, Type 1"
+BMGC_DS16825,BMG_DS065266,Senior-Loken Syndrome 1
+BMGC_DS16826,BMG_DS065267,"AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 1"
+BMGC_DS16827,BMG_DS065268,microcephaly
+BMGC_DS16828,BMG_DS065270,Joubert syndrome 1
+BMGC_DS16829,BMG_DS065271,Cranioectodermal dysplasia
+BMGC_DS16830,BMG_DS065272,"MYOFIBROMATOSIS, INFANTILE, 1"
+BMGC_DS16831,BMG_DS065273,UNCOMBABLE HAIR SYNDROME 1
+BMGC_DS16832,BMG_DS065274,Cerebral cortical atrophy
+BMGC_DS16833,BMG_DS065275,Brain atrophy
+BMGC_DS16834,BMG_DS065276,"ESOPHAGITIS, EOSINOPHILIC, 1"
+BMGC_DS16835,BMG_DS065277,Familial renal hypouricemia
+BMGC_DS16836,BMG_DS065278,"SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1"
+BMGC_DS16837,BMG_DS065280,"Biliary Cirrhosis, Primary, 1"
+BMGC_DS16838,BMG_DS065281,Noonan Syndrome 1
+BMGC_DS16839,BMG_DS065282,"EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1"
+BMGC_DS16840,BMG_DS065283,Idiopathic basal ganglia calcification 1
+BMGC_DS16841,BMG_DS065284,leukonychia totalis
+BMGC_DS16842,BMG_DS065285,Granulocytopenic disorder
+BMGC_DS16843,BMG_DS065286,Ichthyosis Congenita I
+BMGC_DS16844,BMG_DS065287,Recurrent pancreatitis
+BMGC_DS16845,BMG_DS065291,"Erythrocytosis familial, 1"
+BMGC_DS16846,BMG_DS065292,Romano-Ward Syndrome
+BMGC_DS16847,BMG_DS065293,developmental dysplasia of the hip
+BMGC_DS16848,BMG_DS065294,Esophageal Stricture
+BMGC_DS16849,BMG_DS065296,Intraretinal hemorrhage
+BMGC_DS16850,BMG_DS065297,Refractory sideroblastic anemia
+BMGC_DS16851,BMG_DS065299,"Keratoderma, Palmoplantar"
+BMGC_DS16852,BMG_DS065301,"HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1"
+BMGC_DS16853,BMG_DS065303,"Periodontitis, Aggressive, 1"
+BMGC_DS16854,BMG_DS065304,adrenal gland pheochromocytoma
+BMGC_DS16855,BMG_DS065307,Sleep-Disordered Breathing
+BMGC_DS16856,BMG_DS065308,urethral stricture
+BMGC_DS16857,BMG_DS065309,Wolfram Syndrome 1
+BMGC_DS16858,BMG_DS065310,Branchiootorenal Syndrome 1
+BMGC_DS16859,BMG_DS065311,Rod-Cone Dystrophy
+BMGC_DS16860,BMG_DS065312,Pigmentary retinopathy
+BMGC_DS16861,BMG_DS065313,Primary Ciliary Dyskinesia
+BMGC_DS16862,BMG_DS065314,PERRAULT SYNDROME 1
+BMGC_DS16863,BMG_DS065315,Esodeviation
+BMGC_DS16864,BMG_DS065317,"CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1"
+BMGC_DS16865,BMG_DS065318,"Seizures, Benign Familial Infantile, 1"
+BMGC_DS16866,BMG_DS065319,Kleefstra syndrome
+BMGC_DS16867,BMG_DS065320,GALLOWAY-MOWAT SYNDROME 1
+BMGC_DS16868,BMG_DS065321,ZIMMERMANN-LABAND SYNDROME 1
+BMGC_DS16869,BMG_DS065322,Feingold syndrome type 1
+BMGC_DS16870,BMG_DS065323,"Knobloch Syndrome, Type I"
+BMGC_DS16871,BMG_DS065324,RITSCHER-SCHINZEL SYNDROME 1
+BMGC_DS16872,BMG_DS065326,Brugada Syndrome 1
+BMGC_DS16873,BMG_DS065327,Oguchi Disease 1
+BMGC_DS16874,BMG_DS065328,Megaloblastic Anemia 1
+BMGC_DS16875,BMG_DS065329,Deafness-symphalangism syndrome of Herrmann
+BMGC_DS16876,BMG_DS065330,Hereditary progressive muscular dystrophy
+BMGC_DS16877,BMG_DS065331,Median Nerve Entrapment
+BMGC_DS16878,BMG_DS065333,Cornelia de Lange Syndrome 1
+BMGC_DS16879,BMG_DS065334,HYPOPLASTIC LEFT HEART SYNDROME 1
+BMGC_DS16880,BMG_DS065335,Asphyxiating Thoracic Dystrophy 1
+BMGC_DS16881,BMG_DS065336,Vesicoureteral Reflux 1
+BMGC_DS16882,BMG_DS065337,RUBINSTEIN-TAYBI SYNDROME 1
+BMGC_DS16883,BMG_DS065338,Ullrich congenital muscular dystrophy
+BMGC_DS16884,BMG_DS065339,"Telangiectasia, Hereditary Hemorrhagic, Type 1"
+BMGC_DS16885,BMG_DS065340,"Ophthalmoplegia, Progressive Supranuclear"
+BMGC_DS16886,BMG_DS065341,"Supranuclear Palsy, Progressive, 1"
+BMGC_DS16887,BMG_DS065342,VAN DER WOUDE SYNDROME 1
+BMGC_DS16888,BMG_DS065343,"Choroidal Dystrophy, Central Areolar 1"
+BMGC_DS16889,BMG_DS065345,Familial Cold Autoinflammatory Syndrome 1
+BMGC_DS16890,BMG_DS065346,"Cholestasis, progressive familial intrahepatic 1"
+BMGC_DS16891,BMG_DS065347,Summerskill syndrome
+BMGC_DS16892,BMG_DS065348,OTOSCLEROSIS 1
+BMGC_DS16893,BMG_DS065349,"Craniosynostosis, Type 1"
+BMGC_DS16894,BMG_DS065350,Total anomalous pulmonary venous return
+BMGC_DS16895,BMG_DS065352,"Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus"
+BMGC_DS16896,BMG_DS065353,Acute Inflammatory Demyelinating Polyneuropathy
+BMGC_DS16897,BMG_DS065355,VAN MALDERGEM SYNDROME 1
+BMGC_DS16898,BMG_DS065356,inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1
+BMGC_DS16899,BMG_DS065357,"Myopathy, Centronuclear, 1"
+BMGC_DS16900,BMG_DS065358,"MACULAR DYSTROPHY, VITELLIFORM, 1"
+BMGC_DS16901,BMG_DS065359,HYPEREKPLEXIA 1
+BMGC_DS16902,BMG_DS065360,"Loeys-Dietz Syndrome, Type 1a"
+BMGC_DS16903,BMG_DS065361,"epilepsy, familial temporal lobe, 1"
+BMGC_DS16904,BMG_DS065362,"MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1"
+BMGC_DS16905,BMG_DS065363,ATRIAL STANDSTILL 1
+BMGC_DS16906,BMG_DS065364,"Sertoli Cell-Only Syndrome, Type I"
+BMGC_DS16907,BMG_DS065365,familial isolated hyperparathyroidism
+BMGC_DS16908,BMG_DS065366,"ACNE INVERSA, FAMILIAL, 1"
+BMGC_DS16909,BMG_DS065367,"GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS 1"
+BMGC_DS16910,BMG_DS065368,ANAUXETIC DYSPLASIA 1
+BMGC_DS16911,BMG_DS065369,GLUT1 DEFICIENCY SYNDROME 1
+BMGC_DS16912,BMG_DS065370,B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY
+BMGC_DS16913,BMG_DS065371,"Lissencephaly, X-Linked, 1"
+BMGC_DS16914,BMG_DS065372,Bilateral Periventricular Nodular Heterotopia
+BMGC_DS16915,BMG_DS065373,"Marble Bones, Autosomal Recessive"
+BMGC_DS16916,BMG_DS065374,Mosaic variegated aneuploidy syndrome
+BMGC_DS16917,BMG_DS065375,Miyoshi Muscular Dystrophy 1
+BMGC_DS16918,BMG_DS065376,"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 1"
+BMGC_DS16919,BMG_DS065377,RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 1
+BMGC_DS16920,BMG_DS065378,HYPOTRICHOSIS 1
+BMGC_DS16921,BMG_DS065380,HEIMLER SYNDROME 1
+BMGC_DS16922,BMG_DS065381,Familial Multiple Coagulation Factor Deficiency I
+BMGC_DS16923,BMG_DS065382,TRICHOHEPATOENTERIC SYNDROME 1
+BMGC_DS16924,BMG_DS065383,"EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 1"
+BMGC_DS16925,BMG_DS065384,Arthrogryposis with renal dysfunction and cholestasis syndrome
+BMGC_DS16926,BMG_DS065385,"ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1"
+BMGC_DS16927,BMG_DS065386,AMR Syndrome
+BMGC_DS16928,BMG_DS065387,Acrofrontofacionasal Dysostosis 1
+BMGC_DS16929,BMG_DS065388,BLEPHAROCHEILODONTIC SYNDROME 1
+BMGC_DS16930,BMG_DS065390,"Hypobetalipoproteinemia, Familial, 1"
+BMGC_DS16931,BMG_DS065391,ANTERIOR SEGMENT DYSGENESIS 1
+BMGC_DS16932,BMG_DS065392,"Amyotrophic Lateral Sclerosis, Familial"
+BMGC_DS16933,BMG_DS065393,Mitochondrial DNA Depletion Syndrome 1
+BMGC_DS16934,BMG_DS065394,Auriculocondylar syndrome 1
+BMGC_DS16935,BMG_DS065395,"Porencephaly, Type 1, Autosomal Dominant"
+BMGC_DS16936,BMG_DS065396,"MACULAR DYSTROPHY, PATTERNED, 1"
+BMGC_DS16937,BMG_DS065397,Episodic Kinesigenic Dyskinesia 1
+BMGC_DS16938,BMG_DS065398,MEIER-GORLIN SYNDROME 1
+BMGC_DS16939,BMG_DS065399,WEILL-MARCHESANI SYNDROME 1
+BMGC_DS16940,BMG_DS065400,Ehlers-Danlos syndrome progeroid type
+BMGC_DS16941,BMG_DS065401,Distal Myopathy 1
+BMGC_DS16942,BMG_DS065402,Gonadotropin deficiency
+BMGC_DS16943,BMG_DS065404,CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 1
+BMGC_DS16944,BMG_DS065405,"Ciliary Dyskinesia, Primary, 7, With Or Without Situs Inversus"
+BMGC_DS16945,BMG_DS065406,Cortical Dysplasia-Focal Epilepsy Syndrome
+BMGC_DS16946,BMG_DS065407,ABDOMINAL OBESITY-METABOLIC SYNDROME 1
+BMGC_DS16947,BMG_DS065408,"PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 1"
+BMGC_DS16948,BMG_DS065409,"Pulmonary Hypertension, Primary, 1"
+BMGC_DS16949,BMG_DS065410,Infantile Epileptic-Dyskinetic Encephalopathy
+BMGC_DS16950,BMG_DS065411,PSEUDO-TORCH SYNDROME 1
+BMGC_DS16951,BMG_DS065412,Premature Ovarian Failure 1
+BMGC_DS16952,BMG_DS065413,"HYPOCALCEMIA, AUTOSOMAL DOMINANT 1, WITH BARTTER SYNDROME"
+BMGC_DS16953,BMG_DS065414,"Polyarthritis, Juvenile, Rheumatoid Factor Negative"
+BMGC_DS16954,BMG_DS065415,Dowling-Degos disease 1
+BMGC_DS16955,BMG_DS065416,Nevus Sebaceus of Jadassohn
+BMGC_DS16956,BMG_DS065417,Lynch Syndrome
+BMGC_DS16957,BMG_DS065420,Hereditary angioedema with C1Inh (C1 esterase inhibitor) deficiency
+BMGC_DS16958,BMG_DS065423,TAFRO syndrome
+BMGC_DS16959,BMG_DS065438,"Epilepsy, Minor"
+BMGC_DS16960,BMG_DS065441,Cystic Echinococcosis
+BMGC_DS16961,BMG_DS065445,Infantile Obesity
+BMGC_DS16962,BMG_DS065449,Absence Seizure Disorder
+BMGC_DS16963,BMG_DS065452,"Carney complex, trismus, pseudocamptodactyly syndrome"
+BMGC_DS16964,BMG_DS065453,specific language disorder
+BMGC_DS16965,BMG_DS065454,Common Peroneal Nerve Entrapment
+BMGC_DS16966,BMG_DS065455,Leukoencephalopathy with mild cerebellar ataxia and white matter edema
+BMGC_DS16967,BMG_DS065498,"FANCONI ANEMIA, COMPLEMENTATION GROUP S"
+BMGC_DS16968,BMG_DS065499,"AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 3"
+BMGC_DS16969,BMG_DS065500,Pressure injury
+BMGC_DS16970,BMG_DS065501,Amyloidosis cutis dyschromia
+BMGC_DS16971,BMG_DS065505,"PROTOPORPHYRIA, ERYTHROPOIETIC, 1"
+BMGC_DS16972,BMG_DS065506,"TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1"
+BMGC_DS16973,BMG_DS065507,MANDIBULOFACIAL DYSOSTOSIS WITH IMPAIRED INTELLECTUAL DEVELOPMENT
+BMGC_DS16974,BMG_DS065508,SHWACHMAN-DIAMOND SYNDROME 1
+BMGC_DS16975,BMG_DS065509,"intellectual disability, X-linked 107"
+BMGC_DS16976,BMG_DS065510,"blepharospasm, benign essential, susceptibility to"
+BMGC_DS16977,BMG_DS065512,"SEIZURES, BENIGN FAMILIAL INFANTILE, 6"
+BMGC_DS16978,BMG_DS065515,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ibb"
+BMGC_DS16979,BMG_DS065517,"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE"
+BMGC_DS16980,BMG_DS065518,ALKURAYA-KUCINSKAS SYNDROME
+BMGC_DS16981,BMG_DS065520,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 92
+BMGC_DS16982,BMG_DS065521,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58"
+BMGC_DS16983,BMG_DS065522,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 55, WITH SEIZURES"
+BMGC_DS16984,BMG_DS065523,DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES
+BMGC_DS16985,BMG_DS065524,amyotrophic lateral sclerosis type 23
+BMGC_DS16986,BMG_DS065525,"intellectual disability, autosomal dominant 56"
+BMGC_DS16987,BMG_DS065526,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY"
+BMGC_DS16988,BMG_DS065527,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES
+BMGC_DS16989,BMG_DS065528,"NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES"
+BMGC_DS16990,BMG_DS065531,SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY
+BMGC_DS16991,BMG_DS065532,RETINITIS PIGMENTOSA 81
+BMGC_DS16992,BMG_DS065533,Syndromic sensorineural deafness due to combined oxidative phosphorylation defect
+BMGC_DS16993,BMG_DS065534,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35
+BMGC_DS16994,BMG_DS065535,POLYCYSTIC LIVER DISEASE 3 WITH OR WITHOUT KIDNEY CYSTS
+BMGC_DS16995,BMG_DS065536,POLYCYSTIC LIVER DISEASE 4 WITH OR WITHOUT KIDNEY CYSTS
+BMGC_DS16996,BMG_DS065538,LEBER CONGENITAL AMAUROSIS WITH EARLY-ONSET DEAFNESS
+BMGC_DS16997,BMG_DS065539,"CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G"
+BMGC_DS16998,BMG_DS065540,"amyotrophic lateral sclerosis, susceptibility to, 24"
+BMGC_DS16999,BMG_DS065541,SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY
+BMGC_DS17000,BMG_DS065542,MULTIPLE SYNOSTOSES SYNDROME 4
+BMGC_DS17001,BMG_DS065543,"LEUKODYSTROPHY, HYPOMYELINATING, 14"
+BMGC_DS17002,BMG_DS065544,"encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8"
+BMGC_DS17003,BMG_DS065545,NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS
+BMGC_DS17004,BMG_DS065546,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 59
+BMGC_DS17005,BMG_DS065547,"ERYTHROCYTOSIS, FAMILIAL, 5"
+BMGC_DS17006,BMG_DS065548,DIAMOND-BLACKFAN ANEMIA-LIKE
+BMGC_DS17007,BMG_DS065549,"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5"
+BMGC_DS17008,BMG_DS065550,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES"
+BMGC_DS17009,BMG_DS065551,"microcephaly 20, primary, autosomal recessive"
+BMGC_DS17010,BMG_DS065552,"HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME"
+BMGC_DS17011,BMG_DS065553,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7
+BMGC_DS17012,BMG_DS065554,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8
+BMGC_DS17013,BMG_DS065555,"amyotrophic lateral sclerosis, susceptibility to, 25"
+BMGC_DS17014,BMG_DS065556,"epilepsy, juvenile myoclonic, susceptibility to, 10"
+BMGC_DS17015,BMG_DS065557,SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY
+BMGC_DS17016,BMG_DS065558,OROFACIODIGITAL SYNDROME XVII
+BMGC_DS17017,BMG_DS065559,KERATOCONUS 9
+BMGC_DS17018,BMG_DS065560,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 60
+BMGC_DS17019,BMG_DS065561,CHROMOSOME 1p35 DELETION SYNDROME
+BMGC_DS17020,BMG_DS065562,"PUM1-associated developmental disability, ataxia, seizure syndrome"
+BMGC_DS17021,BMG_DS065563,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 61
+BMGC_DS17022,BMG_DS065564,"EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 4"
+BMGC_DS17023,BMG_DS065565,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 62
+BMGC_DS17024,BMG_DS065566,SHWACHMAN-DIAMOND SYNDROME 2
+BMGC_DS17025,BMG_DS065567,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36
+BMGC_DS17026,BMG_DS065568,"LEUKODYSTROPHY, HYPOMYELINATING, 15"
+BMGC_DS17027,BMG_DS065569,"OSTEOGENESIS IMPERFECTA, TYPE XVIII"
+BMGC_DS17028,BMG_DS065570,Multiple mitochondrial dysfunctions syndrome type 6
+BMGC_DS17029,BMG_DS065571,SPERMATOGENIC FAILURE 24
+BMGC_DS17030,BMG_DS065572,SPERMATOGENIC FAILURE 25
+BMGC_DS17031,BMG_DS065574,SPERMATOGENIC FAILURE 26
+BMGC_DS17032,BMG_DS065575,"LEUKODYSTROPHY, HYPOMYELINATING, 16"
+BMGC_DS17033,BMG_DS065576,SPERMATOGENIC FAILURE 27
+BMGC_DS17034,BMG_DS065577,"RH-NULL, AMORPH TYPE"
+BMGC_DS17035,BMG_DS065578,"METHEMOGLOBINEMIA, ALPHA TYPE"
+BMGC_DS17036,BMG_DS065579,"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, DI ROCCO TYPE"
+BMGC_DS17037,BMG_DS065580,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 63
+BMGC_DS17038,BMG_DS065581,NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES
+BMGC_DS17039,BMG_DS065582,"ERYTHROCYTOSIS, FAMILIAL, 6"
+BMGC_DS17040,BMG_DS065583,"ERYTHROCYTOSIS, FAMILIAL, 7"
+BMGC_DS17041,BMG_DS065584,VERVERI-BRADY SYNDROME
+BMGC_DS17042,BMG_DS065585,"MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS17043,BMG_DS065586,"MICROCEPHALY 22, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS17044,BMG_DS065587,"MICROCEPHALY 23, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS17045,BMG_DS065588,JABERI-ELAHI SYNDROME
+BMGC_DS17046,BMG_DS065589,"PHIP-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome"
+BMGC_DS17047,BMG_DS065590,"TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2"
+BMGC_DS17048,BMG_DS065591,"TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 3"
+BMGC_DS17049,BMG_DS065592,oocyte maturation defect 5
+BMGC_DS17050,BMG_DS065593,Classical-like Ehlers-Danlos syndrome type 2
+BMGC_DS17051,BMG_DS065594,"DEAFNESS, AUTOSOMAL RECESSIVE 57"
+BMGC_DS17052,BMG_DS065595,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 64
+BMGC_DS17053,BMG_DS065596,CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION 1
+BMGC_DS17054,BMG_DS065597,"LEUKODYSTROPHY, HYPOMYELINATING, 17"
+BMGC_DS17055,BMG_DS065598,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 65
+BMGC_DS17056,BMG_DS065599,HYPEREKPLEXIA 4
+BMGC_DS17057,BMG_DS065600,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 93
+BMGC_DS17058,BMG_DS065601,"DEAFNESS, AUTOSOMAL RECESSIVE 109"
+BMGC_DS17059,BMG_DS065602,PREMATURE OVARIAN FAILURE 14
+BMGC_DS17060,BMG_DS065603,"PROTOPORPHYRIA, ERYTHROPOIETIC, 2"
+BMGC_DS17061,BMG_DS065604,"DRUG METABOLISM, ALTERED, CYP2C8-RELATED"
+BMGC_DS17062,BMG_DS065616,"METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC"
+BMGC_DS17063,BMG_DS065639,"HEMOGLOBIN M (RADOM) METHEMOGLOBINEMIA, BETA TYPE"
+BMGC_DS17064,BMG_DS065640,POLYCYSTIC OVARY SYNDROME DUE TO 17-KETOSTEROID REDUCTASE DEFICIENCY
+BMGC_DS17065,BMG_DS065642,congenital disorder of glycosylation type I
+BMGC_DS17066,BMG_DS065657,Tessier number 4 facial cleft
+BMGC_DS17067,BMG_DS065658,Severe Cytomegalovirus Infection
+BMGC_DS17068,BMG_DS065665,Stationary Cone Dystrophy
+BMGC_DS17069,BMG_DS065666,"Polyarthritis, Juvenile, Rheumatoid Factor Positive"
+BMGC_DS17070,BMG_DS065667,Genital Vulvovaginal Candidiasis
+BMGC_DS17071,BMG_DS065668,Fibrocystic Dysplasia of Bone
+BMGC_DS17072,BMG_DS065669,Fibrocartilaginous Dysplasia of Bone
+BMGC_DS17073,BMG_DS065670,Maternal Sepsis
+BMGC_DS17074,BMG_DS065671,Posterior Interosseous Nerve Syndrome
+BMGC_DS17075,BMG_DS065672,Femoral Nerve Dysfunction
+BMGC_DS17076,BMG_DS065675,2q33.1 microdeletion syndrome
+BMGC_DS17077,BMG_DS065678,Combined oxidative phosphorylation defect type 13
+BMGC_DS17078,BMG_DS065683,Combined oxidative phosphorylation defect type 15
+BMGC_DS17079,BMG_DS065684,Combined oxidative phosphorylation defect type 9
+BMGC_DS17080,BMG_DS065685,Combined oxidative phosphorylation defect type 21
+BMGC_DS17081,BMG_DS065695,"Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome"
+BMGC_DS17082,BMG_DS065696,acute myeloid leukemia with NPM1 somatic mutations
+BMGC_DS17083,BMG_DS065700,Congenital myopathy with myasthenic-like onset
+BMGC_DS17084,BMG_DS065703,Connective tissue disorder due to lysyl hydroxylase-3 deficiency
+BMGC_DS17085,BMG_DS065704,Lethal congenital contracture syndrome type 5
+BMGC_DS17086,BMG_DS065705,Autosomal recessive cerebellar ataxia with late-onset spasticity
+BMGC_DS17087,BMG_DS065706,Progressive myoclonic epilepsy with dystonia
+BMGC_DS17088,BMG_DS065707,"Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome"
+BMGC_DS17089,BMG_DS065708,Spectrin-associated autosomal recessive cerebellar ataxia
+BMGC_DS17090,BMG_DS065709,"Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome"
+BMGC_DS17091,BMG_DS065710,Familial progressive hyperpigmentation and hypopigmentation of skin
+BMGC_DS17092,BMG_DS065719,Distal monosomy 3p syndrome
+BMGC_DS17093,BMG_DS065722,Hot water reflex epilepsy
+BMGC_DS17094,BMG_DS065728,Severe combined immunodeficiency due to CTPS1 deficiency
+BMGC_DS17095,BMG_DS065732,"Deafness, encephaloneuropathy, obesity, valvulopathy syndrome"
+BMGC_DS17096,BMG_DS065733,Idiopathic CD4 lymphocytopenia
+BMGC_DS17097,BMG_DS065734,Familial hyperprolactinemia
+BMGC_DS17098,BMG_DS065735,familial vesicoureteral reflux
+BMGC_DS17099,BMG_DS065737,Hypermethioninemia encephalopathy due to deficiency of adenosine kinase
+BMGC_DS17100,BMG_DS065738,"Hypotonia, speech impairment, severe cognitive delay syndrome"
+BMGC_DS17101,BMG_DS065740,"Intellectual disability, alacrima, achalasia syndrome"
+BMGC_DS17102,BMG_DS065744,Macrocephaly and developmental delay syndrome
+BMGC_DS17103,BMG_DS065745,KLHL9-related early-onset distal myopathy
+BMGC_DS17104,BMG_DS065746,Larsen-like syndrome B3GAT3 type
+BMGC_DS17105,BMG_DS065749,megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)
+BMGC_DS17106,BMG_DS065750,"Microcephalus, complex motor and sensory axonal neuropathy syndrome"
+BMGC_DS17107,BMG_DS065752,Oculoauricular syndrome Schorderet type
+BMGC_DS17108,BMG_DS065757,Oro-facial digital syndrome type 14
+BMGC_DS17109,BMG_DS065760,SHOX-related short stature
+BMGC_DS17110,BMG_DS065782,Spondyloperipheral dysplasia with short ulna syndrome
+BMGC_DS17111,BMG_DS065785,Short stature with delayed bone age due to thyroid hormone metabolism deficiency
+BMGC_DS17112,BMG_DS065786,"Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome"
+BMGC_DS17113,BMG_DS065787,Male infertility with teratozoospermia due to single gene mutation
+BMGC_DS17114,BMG_DS065795,Wooly hair with palmoplantar keratoderma syndrome
+BMGC_DS17115,BMG_DS065826,Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
+BMGC_DS17116,BMG_DS065837,familial isolated trichomegaly
+BMGC_DS17117,BMG_DS065845,Distal 17p13.3 microdeletion syndrome
+BMGC_DS17118,BMG_DS065849,"Progressive external ophthalmoplegia, myopathy, emaciation syndrome"
+BMGC_DS17119,BMG_DS065853,Autosomal recessive myogenic arthrogryposis multiplex congenita
+BMGC_DS17120,BMG_DS065854,Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
+BMGC_DS17121,BMG_DS065855,acute myeloid leukemia with CEBPA somatic mutations
+BMGC_DS17122,BMG_DS065857,"Tibial hemimelia, polysyndactyly, triphalangeal thumb syndrome"
+BMGC_DS17123,BMG_DS065859,inherited acute myeloid leukemia
+BMGC_DS17124,BMG_DS065860,"Colobomatous microphthalmia, rhizomelic dysplasia syndrome"
+BMGC_DS17125,BMG_DS065861,Congenital myopathy with internal nuclei and atypical cores
+BMGC_DS17126,BMG_DS065865,Striate palmoplantar keratoderma
+BMGC_DS17127,BMG_DS065866,Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency
+BMGC_DS17128,BMG_DS065867,Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
+BMGC_DS17129,BMG_DS065869,Familial thoracic aortic aneurysm and aortic dissection
+BMGC_DS17130,BMG_DS065872,Muscle filaminopathy
+BMGC_DS17131,BMG_DS065878,"Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome"
+BMGC_DS17132,BMG_DS065879,"Rolandic epilepsy, speech dyspraxia syndrome"
+BMGC_DS17133,BMG_DS065881,Methylmalonic acidemia due to methylmalonyl-coenzyme A epimerase deficiency
+BMGC_DS17134,BMG_DS065886,sporadic pheochromocytoma/secreting paraganglioma
+BMGC_DS17135,BMG_DS065887,T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency
+BMGC_DS17136,BMG_DS065890,Severe combined immunodeficiency due to complete RAG1 and/or RAG2 deficiency
+BMGC_DS17137,BMG_DS065892,Familial generalized lentiginosis
+BMGC_DS17138,BMG_DS065893,Distal myotilinopathy
+BMGC_DS17139,BMG_DS065894,Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier
+BMGC_DS17140,BMG_DS065895,familial multiple meningioma
+BMGC_DS17141,BMG_DS065909,"Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome"
+BMGC_DS17142,BMG_DS065929,Acute encephalopathy with biphasic seizures and late reduced diffusion
+BMGC_DS17143,BMG_DS065933,Distal monosomy 15q
+BMGC_DS17144,BMG_DS065953,Multiple epiphyseal dysplasia due to collagen 9 anomaly
+BMGC_DS17145,BMG_DS065962,1p31p32 microdeletion syndrome
+BMGC_DS17146,BMG_DS065963,Autosomal recessive spastic paraplegia type 67
+BMGC_DS17147,BMG_DS065968,Short stature due to growth hormone secretagogue receptor deficiency
+BMGC_DS17148,BMG_DS065969,X-linked non progressive cerebellar ataxia
+BMGC_DS17149,BMG_DS065971,"Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome"
+BMGC_DS17150,BMG_DS065974,Diencephalic mesencephalic junction dysplasia
+BMGC_DS17151,BMG_DS065977,Combined immunodeficiency due to OX40 deficiency
+BMGC_DS17152,BMG_DS065978,Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
+BMGC_DS17153,BMG_DS065980,Hypomyelination neuropathy arthrogryposis syndrome
+BMGC_DS17154,BMG_DS065983,isolated unilateral hemispheric cerebellar hypoplasia
+BMGC_DS17155,BMG_DS065986,Severe early-onset axonal neuropathy due to mitofusin 2 deficiency
+BMGC_DS17156,BMG_DS065991,Immunodeficiency due to ficolin 3 deficiency
+BMGC_DS17157,BMG_DS066017,Anemia due to and following chemotherapy
+BMGC_DS17158,BMG_DS066048,PURA syndrome
+BMGC_DS17159,BMG_DS066052,5q31.3 microdeletion syndrome
+BMGC_DS17160,BMG_DS066077,coloboma of choroid and retina
+BMGC_DS17161,BMG_DS066092,Vaso-occlusive pain episode in sickle cell disease
+BMGC_DS17162,BMG_DS066184,Heterophoria
+BMGC_DS17163,BMG_DS066185,"Angioma serpiginosum, X-linked"
+BMGC_DS17164,BMG_DS066188,mantle cell lymphoma
+BMGC_DS17165,BMG_DS066189,"thyroid cancer, nonmedullary, 1"
+BMGC_DS17166,BMG_DS066190,"NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE"
+BMGC_DS17167,BMG_DS066191,"Charcot-Marie-Tooth disease, Type 4E"
+BMGC_DS17168,BMG_DS066196,Peripheral Nervous System Diseases
+BMGC_DS17169,BMG_DS066197,Peripheral dysostosis
+BMGC_DS17170,BMG_DS066199,"Alveolitis, Fibrosing"
+BMGC_DS17171,BMG_DS066200,Usual Interstitial Pneumonia
+BMGC_DS17172,BMG_DS066201,"lymphoma, non-Hodgkin, familial"
+BMGC_DS17173,BMG_DS066202,PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
+BMGC_DS17174,BMG_DS066203,Autosomal dominant neovascular inflammatory vitreoretinopathy
+BMGC_DS17175,BMG_DS066204,Autoimmune hepatitis
+BMGC_DS17176,BMG_DS066205,ovarian carcinoma
+BMGC_DS17177,BMG_DS066207,Citrullinemia Type 1
+BMGC_DS17178,BMG_DS066210,skin basal cell carcinoma
+BMGC_DS17179,BMG_DS066212,"Marfan Syndrome, Type I"
+BMGC_DS17180,BMG_DS066213,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 1"
+BMGC_DS17181,BMG_DS066214,"MYOPATHY, MYOFIBRILLAR, 4"
+BMGC_DS17182,BMG_DS066215,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A"
+BMGC_DS17183,BMG_DS066216,Congenital External Ophthalmoplegia
+BMGC_DS17184,BMG_DS066217,SPERMATOGENIC FAILURE 3
+BMGC_DS17185,BMG_DS066218,"CATARACT 2, MULTIPLE TYPES"
+BMGC_DS17186,BMG_DS066219,"HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT"
+BMGC_DS17187,BMG_DS066221,POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 1
+BMGC_DS17188,BMG_DS066222,Hereditary Motor-Sensory Neuropathy with Pyramidal Signs
+BMGC_DS17189,BMG_DS066224,Familial Idiopathic Pulmonary Fibrosis
+BMGC_DS17190,BMG_DS066228,Hypoprothrombinemias
+BMGC_DS17191,BMG_DS066229,"epidermodysplasia verruciformis, susceptibility to, 2"
+BMGC_DS17192,BMG_DS066230,"ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IV"
+BMGC_DS17193,BMG_DS066232,"NEUROPATHY, CONGENITAL HYPOMYELINATING, 2"
+BMGC_DS17194,BMG_DS066234,"HYPER-IgE RECURRENT INFECTION SYNDROME 2, AUTOSOMAL RECESSIVE"
+BMGC_DS17195,BMG_DS066237,"prostate cancer, hereditary, 1"
+BMGC_DS17196,BMG_DS066239,Generalized Thyroid Hormone Resistance
+BMGC_DS17197,BMG_DS066242,MOYAMOYA DISEASE 6 WITH ACHALASIA
+BMGC_DS17198,BMG_DS066243,"ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION"
+BMGC_DS17199,BMG_DS066244,PLCG2-associated antibody deficiency and immune dysregulation
+BMGC_DS17200,BMG_DS066247,"epidermodysplasia verruciformis, susceptibility to, 1"
+BMGC_DS17201,BMG_DS066252,telomere syndrome
+BMGC_DS17202,BMG_DS066256,PIK3CA-related overgrowth spectrum
+BMGC_DS17203,BMG_DS066278,LYMPHATIC MALFORMATION 5
+BMGC_DS17204,BMG_DS066279,"ALPORT SYNDROME 2, AUTOSOMAL RECESSIVE"
+BMGC_DS17205,BMG_DS066280,"MICROCEPHALY, GROWTH RESTRICTION, AND INCREASED SISTER CHROMATID EXCHANGE 1"
+BMGC_DS17206,BMG_DS066281,ORTHOSTATIC HYPOTENSION 1
+BMGC_DS17207,BMG_DS066284,proteasome-associated autoinflammatory syndrome 1
+BMGC_DS17208,BMG_DS066290,"osteogenesis imperfecta, type 19"
+BMGC_DS17209,BMG_DS066291,"HEMOLYTIC ANEMIA, CONGENITAL, X-LINKED"
+BMGC_DS17210,BMG_DS066292,"DEAFNESS, X-LINKED 7"
+BMGC_DS17211,BMG_DS066293,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12"
+BMGC_DS17212,BMG_DS066294,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 30"
+BMGC_DS17213,BMG_DS066295,"ALPORT SYNDROME 1, X-LINKED"
+BMGC_DS17214,BMG_DS066296,"MITOCHONDRIAL COMPLEX I DEFICIENCY, MITOCHONDRIAL TYPE 1"
+BMGC_DS17215,BMG_DS066297,CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 1
+BMGC_DS17216,BMG_DS066298,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20"
+BMGC_DS17217,BMG_DS066299,LYMPHATIC MALFORMATION 2
+BMGC_DS17218,BMG_DS066301,LYMPHATIC MALFORMATION 3
+BMGC_DS17219,BMG_DS066302,"short-rib thoracic dysplasia 7/20 with polydactyly, digenic"
+BMGC_DS17220,BMG_DS066303,autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
+BMGC_DS17221,BMG_DS066304,RETINITIS PIGMENTOSA 82 WITH OR WITHOUT SITUS INVERSUS
+BMGC_DS17222,BMG_DS066305,IMMUNODEFICIENCY 15B
+BMGC_DS17223,BMG_DS066306,LYMPHATIC MALFORMATION 4
+BMGC_DS17224,BMG_DS066308,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3
+BMGC_DS17225,BMG_DS066309,"HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES"
+BMGC_DS17226,BMG_DS066310,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17
+BMGC_DS17227,BMG_DS066311,Regressive spondylometaphyseal dysplasia
+BMGC_DS17228,BMG_DS066312,TETRAAMELIA SYNDROME 2
+BMGC_DS17229,BMG_DS066313,humerofemoral hypoplasia with radiotibial ray deficiency
+BMGC_DS17230,BMG_DS066314,COFFIN-SIRIS SYNDROME 7
+BMGC_DS17231,BMG_DS066315,"CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 4"
+BMGC_DS17232,BMG_DS066316,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2DD"
+BMGC_DS17233,BMG_DS066317,IMMUNODEFICIENCY 100 WITH PULMONARY ALVEOLAR PROTEINOSIS AND HYPOGAMMAGLOBULINEMIA
+BMGC_DS17234,BMG_DS066318,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2
+BMGC_DS17235,BMG_DS066319,infantile parkinsonism-dystonia 2
+BMGC_DS17236,BMG_DS066320,"intellectual disability, autosomal dominant 57"
+BMGC_DS17237,BMG_DS066321,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 27"
+BMGC_DS17238,BMG_DS066322,NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES
+BMGC_DS17239,BMG_DS066323,INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA
+BMGC_DS17240,BMG_DS066324,POLYCYSTIC KIDNEY DISEASE 6 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE
+BMGC_DS17241,BMG_DS066325,"CILIARY DYSKINESIA, PRIMARY, 38"
+BMGC_DS17242,BMG_DS066326,"PONTOCEREBELLAR HYPOPLASIA, TYPE 1D"
+BMGC_DS17243,BMG_DS066327,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 66
+BMGC_DS17244,BMG_DS066328,"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 6"
+BMGC_DS17245,BMG_DS066329,"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 7"
+BMGC_DS17246,BMG_DS066330,NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH
+BMGC_DS17247,BMG_DS066331,INFLAMMATORY BOWEL DISEASE 29
+BMGC_DS17248,BMG_DS066332,OVARIAN DYSGENESIS 6
+BMGC_DS17249,BMG_DS066333,PEELING SKIN SYNDROME 6
+BMGC_DS17250,BMG_DS066334,SPERMATOGENIC FAILURE 28
+BMGC_DS17251,BMG_DS066336,"SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS"
+BMGC_DS17252,BMG_DS066337,"NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES"
+BMGC_DS17253,BMG_DS066338,INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES
+BMGC_DS17254,BMG_DS066339,NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM
+BMGC_DS17255,BMG_DS066340,SPERMATOGENIC FAILURE 29
+BMGC_DS17256,BMG_DS066341,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES"
+BMGC_DS17257,BMG_DS066342,SPINOCEREBELLAR ATAXIA 48
+BMGC_DS17258,BMG_DS066343,"DEAFNESS, AUTOSOMAL RECESSIVE 110"
+BMGC_DS17259,BMG_DS066344,"intellectual disability, autosomal recessive 63"
+BMGC_DS17260,BMG_DS066345,PREMATURE OVARIAN FAILURE 15
+BMGC_DS17261,BMG_DS066346,"MICROCEPHALY, GROWTH RESTRICTION, AND INCREASED SISTER CHROMATID EXCHANGE 2"
+BMGC_DS17262,BMG_DS066347,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5"
+BMGC_DS17263,BMG_DS066348,"intellectual disability, autosomal recessive 64"
+BMGC_DS17264,BMG_DS066349,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 58"
+BMGC_DS17265,BMG_DS066350,"OSTEOPETROSIS, AUTOSOMAL DOMINANT 3"
+BMGC_DS17266,BMG_DS066351,IMMUNODEFICIENCY 57 WITH AUTOINFLAMMATION
+BMGC_DS17267,BMG_DS066352,"intellectual disability, autosomal recessive 65"
+BMGC_DS17268,BMG_DS066353,SPERMATOGENIC FAILURE 30
+BMGC_DS17269,BMG_DS066354,SPERMATOGENIC FAILURE 31
+BMGC_DS17270,BMG_DS066355,LIDDLE SYNDROME 2
+BMGC_DS17271,BMG_DS066356,SPERMATOGENIC FAILURE 32
+BMGC_DS17272,BMG_DS066357,BONE MARROW FAILURE SYNDROME 4
+BMGC_DS17273,BMG_DS066359,OVARIAN DYSGENESIS 7
+BMGC_DS17274,BMG_DS066360,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5"
+BMGC_DS17275,BMG_DS066361,"polydactyly, postaxial, type A8"
+BMGC_DS17276,BMG_DS066362,"PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT"
+BMGC_DS17277,BMG_DS066363,LIDDLE SYNDROME 3
+BMGC_DS17278,BMG_DS066364,Calpain-3-related limb girdle muscular dystrophy D4
+BMGC_DS17279,BMG_DS066365,IMMUNODEFICIENCY 58
+BMGC_DS17280,BMG_DS066366,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8"
+BMGC_DS17281,BMG_DS066367,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23"
+BMGC_DS17282,BMG_DS066368,"DEAFNESS, AUTOSOMAL DOMINANT 74"
+BMGC_DS17283,BMG_DS066369,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 67
+BMGC_DS17284,BMG_DS066370,"MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME"
+BMGC_DS17285,BMG_DS066371,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 95
+BMGC_DS17286,BMG_DS066372,"USHER SYNDROME, TYPE IV"
+BMGC_DS17287,BMG_DS066373,"DEAFNESS, AUTOSOMAL RECESSIVE 111"
+BMGC_DS17288,BMG_DS066374,INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES
+BMGC_DS17289,BMG_DS066375,Autosomal recessive extra-oral halitosis
+BMGC_DS17290,BMG_DS066376,SPERMATOGENIC FAILURE 33
+BMGC_DS17291,BMG_DS066377,SPERMATOGENIC FAILURE 34
+BMGC_DS17292,BMG_DS066378,HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 3
+BMGC_DS17293,BMG_DS066379,"OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES"
+BMGC_DS17294,BMG_DS066380,SQUALENE SYNTHASE DEFICIENCY
+BMGC_DS17295,BMG_DS066381,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY"
+BMGC_DS17296,BMG_DS066382,"PITUITARY HORMONE DEFICIENCY, COMBINED OR ISOLATED, 7"
+BMGC_DS17297,BMG_DS066383,JOUBERT SYNDROME 35
+BMGC_DS17298,BMG_DS066384,"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE"
+BMGC_DS17299,BMG_DS066385,"cardiac, facial, and digital anomalies with developmental delay"
+BMGC_DS17300,BMG_DS066386,BONE MARROW FAILURE SYNDROME 5
+BMGC_DS17301,BMG_DS066387,"OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS"
+BMGC_DS17302,BMG_DS066388,DIARRHEA 9
+BMGC_DS17303,BMG_DS066389,"NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES"
+BMGC_DS17304,BMG_DS066390,RETINITIS PIGMENTOSA 83
+BMGC_DS17305,BMG_DS066391,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9"
+BMGC_DS17306,BMG_DS066392,"NEPHROTIC SYNDROME, TYPE 17"
+BMGC_DS17307,BMG_DS066393,"NEPHROTIC SYNDROME, TYPE 18"
+BMGC_DS17308,BMG_DS066394,"NEPHROTIC SYNDROME, TYPE 19"
+BMGC_DS17309,BMG_DS066395,"MICROCEPHALY 24, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS17310,BMG_DS066396,"ECTODERMAL DYSPLASIA 14, HAIR/TOOTH TYPE, WITH OR WITHOUT HYPOHIDROSIS"
+BMGC_DS17311,BMG_DS066399,ORTHOSTATIC HYPOTENSION 2
+BMGC_DS17312,BMG_DS066400,"DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE"
+BMGC_DS17313,BMG_DS066401,PERIVENTRICULAR NODULAR HETEROTOPIA 8
+BMGC_DS17314,BMG_DS066402,"NEUROPATHY, CONGENITAL HYPOMYELINATING, 3"
+BMGC_DS17315,BMG_DS066403,OVARIAN DYSGENESIS 8
+BMGC_DS17316,BMG_DS066404,"CARDIOMYOPATHY, DILATED, 2C"
+BMGC_DS17317,BMG_DS066405,POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2
+BMGC_DS17318,BMG_DS066406,INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA
+BMGC_DS17319,BMG_DS066407,CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 2
+BMGC_DS17320,BMG_DS066408,"MYASTHENIC SYNDROME, CONGENITAL, 23, PRESYNAPTIC"
+BMGC_DS17321,BMG_DS066409,"MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC"
+BMGC_DS17322,BMG_DS066410,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 68
+BMGC_DS17323,BMG_DS066411,IMMUNODEFICIENCY 15A
+BMGC_DS17324,BMG_DS066412,Snijders Blok-Campeau syndrome
+BMGC_DS17325,BMG_DS066413,"INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY"
+BMGC_DS17326,BMG_DS066414,"Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome"
+BMGC_DS17327,BMG_DS066415,"polydactyly, postaxial, type A9"
+BMGC_DS17328,BMG_DS066416,RETINITIS PIGMENTOSA 84
+BMGC_DS17329,BMG_DS066417,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 66"
+BMGC_DS17330,BMG_DS066418,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2"
+BMGC_DS17331,BMG_DS066419,VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION
+BMGC_DS17332,BMG_DS066420,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3"
+BMGC_DS17333,BMG_DS066421,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4"
+BMGC_DS17334,BMG_DS066422,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5"
+BMGC_DS17335,BMG_DS066423,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6"
+BMGC_DS17336,BMG_DS066424,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7"
+BMGC_DS17337,BMG_DS066425,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 8"
+BMGC_DS17338,BMG_DS066426,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 9"
+BMGC_DS17339,BMG_DS066427,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10"
+BMGC_DS17340,BMG_DS066428,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11"
+BMGC_DS17341,BMG_DS066429,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13"
+BMGC_DS17342,BMG_DS066430,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14"
+BMGC_DS17343,BMG_DS066431,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15"
+BMGC_DS17344,BMG_DS066433,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16"
+BMGC_DS17345,BMG_DS066434,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17"
+BMGC_DS17346,BMG_DS066435,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18"
+BMGC_DS17347,BMG_DS066436,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19"
+BMGC_DS17348,BMG_DS066437,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21"
+BMGC_DS17349,BMG_DS066438,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22"
+BMGC_DS17350,BMG_DS066439,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 23"
+BMGC_DS17351,BMG_DS066440,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 24"
+BMGC_DS17352,BMG_DS066441,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25"
+BMGC_DS17353,BMG_DS066442,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26"
+BMGC_DS17354,BMG_DS066443,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 27"
+BMGC_DS17355,BMG_DS066444,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28"
+BMGC_DS17356,BMG_DS066445,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 29"
+BMGC_DS17357,BMG_DS066446,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 31"
+BMGC_DS17358,BMG_DS066447,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 32"
+BMGC_DS17359,BMG_DS066448,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33"
+BMGC_DS17360,BMG_DS066449,"CILIARY DYSKINESIA, PRIMARY, 39"
+BMGC_DS17361,BMG_DS066450,"DEAFNESS, AUTOSOMAL RECESSIVE 112"
+BMGC_DS17362,BMG_DS066451,MIRROR MOVEMENTS 4
+BMGC_DS17363,BMG_DS066453,"ARTHROGRYPOSIS, CLEFT PALATE, CRANIOSYNOSTOSIS, AND IMPAIRED INTELLECTUAL DEVELOPMENT"
+BMGC_DS17364,BMG_DS066454,"PONTOCEREBELLAR HYPOPLASIA, TYPE 12"
+BMGC_DS17365,BMG_DS066455,"epidermodysplasia verruciformis, susceptibility to, 3"
+BMGC_DS17366,BMG_DS066456,TRICHOHEPATONEURODEVELOPMENTAL SYNDROME
+BMGC_DS17367,BMG_DS066457,congenital anomalies of kidney and urinary tract 3
+BMGC_DS17368,BMG_DS066458,"Global developmental delay, lung cysts, overgrowth, Wilms tumor syndrome"
+BMGC_DS17369,BMG_DS066459,MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS
+BMGC_DS17370,BMG_DS066460,HYPOTRICHOSIS 14
+BMGC_DS17371,BMG_DS066461,"NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY"
+BMGC_DS17372,BMG_DS066462,"FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS"
+BMGC_DS17373,BMG_DS066463,"CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1G"
+BMGC_DS17374,BMG_DS066464,Cardiac urogenital syndrome
+BMGC_DS17375,BMG_DS066465,"HYPER-IgE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE"
+BMGC_DS17376,BMG_DS066466,VISUAL IMPAIRMENT AND PROGRESSIVE PHTHISIS BULBI
+BMGC_DS17377,BMG_DS066467,"MICROCEPHALY, CATARACTS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSTONIA WITH ABNORMAL STRIATUM"
+BMGC_DS17378,BMG_DS066468,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 69
+BMGC_DS17379,BMG_DS066469,"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT"
+BMGC_DS17380,BMG_DS066470,"AUTOINFLAMMATORY DISEASE, FAMILIAL, BEHCET-LIKE 3"
+BMGC_DS17381,BMG_DS066471,"SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT"
+BMGC_DS17382,BMG_DS066472,"NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA"
+BMGC_DS17383,BMG_DS066473,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 67"
+BMGC_DS17384,BMG_DS066474,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 70
+BMGC_DS17385,BMG_DS066475,"CILIARY DYSKINESIA, PRIMARY, 40"
+BMGC_DS17386,BMG_DS066476,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68"
+BMGC_DS17387,BMG_DS066477,"epidermodysplasia verruciformis, susceptibility to, 4"
+BMGC_DS17388,BMG_DS066478,"epidermodysplasia verruciformis, susceptibility to, 5"
+BMGC_DS17389,BMG_DS066483,"PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1, DIGENIC"
+BMGC_DS17390,BMG_DS066508,"MASTOCYTOSIS, CUTANEOUS AND SYSTEMIC, SOMATIC"
+BMGC_DS17391,BMG_DS066510,"MASTOCYTOSIS, INDOLENT"
+BMGC_DS17392,BMG_DS066511,MASTOCYTOSIS WITH ASSOCIATED HEMATOLOGIC DISORDER
+BMGC_DS17393,BMG_DS066512,"NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL DOMINANT"
+BMGC_DS17394,BMG_DS066513,CHROMOSOME 1p36.11 DUPLICATION SYNDROME
+BMGC_DS17395,BMG_DS066514,"PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3, DIGENIC"
+BMGC_DS17396,BMG_DS066515,CARBOXYLESTERASE 1 DEFICIENCY
+BMGC_DS17397,BMG_DS066516,CHROMOSOME 14q32 DELETION SYNDROME
+BMGC_DS17398,BMG_DS066540,Autosomal recessive chorioretinopathy and microcephaly syndrome
+BMGC_DS17399,BMG_DS066541,Benign familial mesial temporal lobe epilepsy
+BMGC_DS17400,BMG_DS066542,Chuvash erythrocytosis
+BMGC_DS17401,BMG_DS066546,Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
+BMGC_DS17402,BMG_DS066549,familial bicuspid aortic valve
+BMGC_DS17403,BMG_DS066556,lissencephaly due to LIS1 mutation
+BMGC_DS17404,BMG_DS066558,Microcephalic primordial dwarfism Dauber type
+BMGC_DS17405,BMG_DS066559,Monosomy 13q14 syndrome
+BMGC_DS17406,BMG_DS066568,"Macular Dystrophy, Retinal, 2"
+BMGC_DS17407,BMG_DS066576,Genetic transient congenital hypothyroidism
+BMGC_DS17408,BMG_DS066603,Vasculitis due to adenosine deaminase 2 deficiency
+BMGC_DS17409,BMG_DS066610,"Microcephaly, thin corpus callosum, intellectual disability syndrome"
+BMGC_DS17410,BMG_DS066611,Proximal myopathy with extrapyramidal signs
+BMGC_DS17411,BMG_DS066612,Autosomal recessive spastic paraplegia type 70
+BMGC_DS17412,BMG_DS066613,Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
+BMGC_DS17413,BMG_DS066614,Female infertility due to zona pellucida defect
+BMGC_DS17414,BMG_DS066615,Spinal muscular atrophy with respiratory distress type 2
+BMGC_DS17415,BMG_DS066618,"Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome"
+BMGC_DS17416,BMG_DS066619,2p21 microdeletion syndrome without cystinuria
+BMGC_DS17417,BMG_DS066620,"Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome"
+BMGC_DS17418,BMG_DS066623,Autosomal dominant intermediate Charcot-Marie-Tooth disease type F
+BMGC_DS17419,BMG_DS066641,T-cell immunodeficiency with epidermodysplasia verruciformis
+BMGC_DS17420,BMG_DS066643,Benign Samaritan congenital myopathy
+BMGC_DS17421,BMG_DS066644,"Tall stature, scoliosis, macrodactyly of great toe syndrome"
+BMGC_DS17422,BMG_DS066645,Developmental delay with autism spectrum disorder and gait instability
+BMGC_DS17423,BMG_DS066646,Adult-onset distal myopathy due to valosin containing protein mutation
+BMGC_DS17424,BMG_DS066647,5p13 microduplication syndrome
+BMGC_DS17425,BMG_DS066658,MITF-related melanoma and renal cell carcinoma predisposition syndrome
+BMGC_DS17426,BMG_DS066660,"Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome"
+BMGC_DS17427,BMG_DS066661,Distal monosomy 12p
+BMGC_DS17428,BMG_DS066675,Autosomal dominant severe congenital neutropenia
+BMGC_DS17429,BMG_DS066677,"Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome"
+BMGC_DS17430,BMG_DS066681,Immunodeficiency due to MASP-2 deficiency
+BMGC_DS17431,BMG_DS066682,hereditary site-specific ovarian cancer syndrome
+BMGC_DS17432,BMG_DS066683,Distal hereditary motor neuropathy type 7
+BMGC_DS17433,BMG_DS066706,"Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome"
+BMGC_DS17434,BMG_DS066707,Charcot-Marie-Tooth disease type 2B5
+BMGC_DS17435,BMG_DS066708,"Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome"
+BMGC_DS17436,BMG_DS066710,"Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome"
+BMGC_DS17437,BMG_DS066711,Ectodermal dysplasia syndactyly syndrome
+BMGC_DS17438,BMG_DS066713,15q11.2 microdeletion syndrome
+BMGC_DS17439,BMG_DS066714,14q11.2 microduplication syndrome
+BMGC_DS17440,BMG_DS066715,"Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome"
+BMGC_DS17441,BMG_DS066717,Methylmalonic aciduria due to transcobalamin receptor defect
+BMGC_DS17442,BMG_DS066720,Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency
+BMGC_DS17443,BMG_DS066721,"Optic nerve edema, splenomegaly syndrome"
+BMGC_DS17444,BMG_DS066722,Developmental and speech delay due to SOX5 deficiency
+BMGC_DS17445,BMG_DS066724,gastric adenocarcinoma and proximal polyposis of the stomach
+BMGC_DS17446,BMG_DS066725,Young adult-onset distal hereditary motor neuropathy
+BMGC_DS17447,BMG_DS066728,Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
+BMGC_DS17448,BMG_DS066729,Combined immunodeficiency due to STK4 deficiency
+BMGC_DS17449,BMG_DS066732,X-linked central congenital hypothyroidism with late-onset testicular enlargement
+BMGC_DS17450,BMG_DS066733,Thrombocythemia with distal limb defect
+BMGC_DS17451,BMG_DS066734,Autism spectrum disorder due to AUTS2 deficiency
+BMGC_DS17452,BMG_DS066735,Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency
+BMGC_DS17453,BMG_DS066736,"Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome"
+BMGC_DS17454,BMG_DS066737,"Facial dysmorphism, immunodeficiency, livedo, short stature syndrome"
+BMGC_DS17455,BMG_DS066738,Severe combined immunodeficiency due to CARD11 deficiency
+BMGC_DS17456,BMG_DS066874,Cyclin-dependent kinase-like 5 deficiency
+BMGC_DS17457,BMG_DS066904,"Microcephaly, polymicrogyria, corpus callosum agenesis syndrome"
+BMGC_DS17458,BMG_DS066905,Congenital lethal myopathy Compton North type
+BMGC_DS17459,BMG_DS066906,Autosomal recessive intermediate Charcot-Marie-Tooth disease type A
+BMGC_DS17460,BMG_DS066909,7q31 microdeletion syndrome
+BMGC_DS17461,BMG_DS066911,Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
+BMGC_DS17462,BMG_DS066912,Autosomal systemic lupus erythematosus
+BMGC_DS17463,BMG_DS066913,Oligodontia and cancer predisposition syndrome
+BMGC_DS17464,BMG_DS066917,"Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome"
+BMGC_DS17465,BMG_DS066919,Bainbridge-Ropers syndrome
+BMGC_DS17466,BMG_DS066920,Intellectual disability with strabismus syndrome
+BMGC_DS17467,BMG_DS066922,Autosomal recessive intermediate Charcot-Marie-Tooth disease type C
+BMGC_DS17468,BMG_DS066924,XYLT1-CDG - xylosyltransferase 1 congenital disorder of glycosylation
+BMGC_DS17469,BMG_DS066926,"Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome"
+BMGC_DS17470,BMG_DS066928,Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
+BMGC_DS17471,BMG_DS066929,East Texas bleeding disorder
+BMGC_DS17472,BMG_DS066930,Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency
+BMGC_DS17473,BMG_DS066932,Autosomal recessive spastic paraplegia type 59
+BMGC_DS17474,BMG_DS066933,LMNA-related cardiocutaneous progeria syndrome
+BMGC_DS17475,BMG_DS066943,Combined immunodeficiency due to MALT1 deficiency
+BMGC_DS17476,BMG_DS066944,Hereditary cryohydrocytosis with normal stomatin
+BMGC_DS17477,BMG_DS066950,"Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome"
+BMGC_DS17478,BMG_DS066951,"Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency"
+BMGC_DS17479,BMG_DS066954,Epidermolysis bullosa simplex due to BP230 deficiency
+BMGC_DS17480,BMG_DS066955,Epidermolysis bullosa simplex due to exophilin 5 deficiency
+BMGC_DS17481,BMG_DS066965,"Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome"
+BMGC_DS17482,BMG_DS066966,Maternal riboflavin deficiency
+BMGC_DS17483,BMG_DS066967,"Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome"
+BMGC_DS17484,BMG_DS066968,"Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome"
+BMGC_DS17485,BMG_DS066969,Severe neurodegenerative syndrome with lipodystrophy
+BMGC_DS17486,BMG_DS066974,Progressive retinal dystrophy due to retinol transport defect
+BMGC_DS17487,BMG_DS066975,"Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome"
+BMGC_DS17488,BMG_DS066977,Congenital chronic diarrhea with protein-losing enteropathy
+BMGC_DS17489,BMG_DS066980,"X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome"
+BMGC_DS17490,BMG_DS067000,"Porencephaly, microcephaly, bilateral congenital cataract syndrome"
+BMGC_DS17491,BMG_DS067001,"Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome"
+BMGC_DS17492,BMG_DS067013,"Multiple congenital anomalies, hypotonia, seizures syndrome type 2"
+BMGC_DS17493,BMG_DS067014,"Progeroid and marfanoid aspect, lipodystrophy syndrome"
+BMGC_DS17494,BMG_DS067016,"Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome"
+BMGC_DS17495,BMG_DS067017,"Congenital cataract, hearing loss, severe developmental delay syndrome"
+BMGC_DS17496,BMG_DS067018,Transient infantile hypertriglyceridemia and hepatosteatosis
+BMGC_DS17497,BMG_DS067019,Neonatal inflammatory skin and bowel disease
+BMGC_DS17498,BMG_DS067021,"Deficiency in anterior pituitary function, variable immunodeficiency syndrome"
+BMGC_DS17499,BMG_DS067023,Hypoinsulinemic hypoglycemia and body hemihypertrophy
+BMGC_DS17500,BMG_DS067024,"Hypertelorism, preauricular sinus, punctual pits, deafness syndrome"
+BMGC_DS17501,BMG_DS067026,"Lethal occipital encephalocele, skeletal dysplasia syndrome"
+BMGC_DS17502,BMG_DS067027,"Hypoplasia of pancreas, intestinal atresia, hypoplasia of gallbladder syndrome"
+BMGC_DS17503,BMG_DS067028,Childhood encephalopathy due to thiamine pyrophosphokinase deficiency
+BMGC_DS17504,BMG_DS067052,Pitt-Hopkins-like syndrome
+BMGC_DS17505,BMG_DS067060,Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency
+BMGC_DS17506,BMG_DS067061,Osteopetrosis hypogammaglobulinemia syndrome
+BMGC_DS17507,BMG_DS067072,Rare isolated myopia
+BMGC_DS17508,BMG_DS067104,isolated asymptomatic elevation of creatine phosphokinase
+BMGC_DS17509,BMG_DS067111,PRKAR1B-related neurodegenerative dementia with intermediate filaments
+BMGC_DS17510,BMG_DS067112,"FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome"
+BMGC_DS17511,BMG_DS067113,Pancytopenia with developmental delay syndrome
+BMGC_DS17512,BMG_DS067127,"Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome"
+BMGC_DS17513,BMG_DS067128,Ferro-cerebro-cutaneous syndrome
+BMGC_DS17514,BMG_DS067129,Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies
+BMGC_DS17515,BMG_DS067130,Periodic paralysis with transient compartment-like syndrome
+BMGC_DS17516,BMG_DS067131,Periodic paralysis with later-onset distal motor neuropathy
+BMGC_DS17517,BMG_DS067132,"Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome"
+BMGC_DS17518,BMG_DS067133,"Intellectual disability, severe speech delay, mild dysmorphism syndrome"
+BMGC_DS17519,BMG_DS067134,"Growth retardation, mild developmental delay, chronic hepatitis syndrome"
+BMGC_DS17520,BMG_DS067135,"Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome"
+BMGC_DS17521,BMG_DS067136,Fatal post-viral neurodegenerative disorder
+BMGC_DS17522,BMG_DS067137,Acute infantile liver failure with multisystemic involvement syndrome
+BMGC_DS17523,BMG_DS067141,"Microcornea, myopic chorioretinal atrophy, telecanthus syndrome"
+BMGC_DS17524,BMG_DS067143,"Congenital neutropenia, myelofibrosis, nephromegaly syndrome"
+BMGC_DS17525,BMG_DS067144,Autosomal recessive cerebral atrophy
+BMGC_DS17526,BMG_DS067146,Hypomyelination with brain stem and spinal cord involvement and leg spasticity
+BMGC_DS17527,BMG_DS067148,KCNQ2-related epileptic encephalopathy
+BMGC_DS17528,BMG_DS067149,Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
+BMGC_DS17529,BMG_DS067151,Autosomal dominant aplasia and myelodysplasia
+BMGC_DS17530,BMG_DS067152,12p12.1 microdeletion syndrome
+BMGC_DS17531,BMG_DS067153,FGFR2-related bent bone dysplasia
+BMGC_DS17532,BMG_DS067155,"Skin fragility, wooly hair, palmoplantar keratoderma syndrome"
+BMGC_DS17533,BMG_DS067156,Severe intellectual disability and progressive spastic paraplegia
+BMGC_DS17534,BMG_DS067160,"Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome"
+BMGC_DS17535,BMG_DS067161,Syndromic multisystem autoimmune disease due to ITCH deficiency
+BMGC_DS17536,BMG_DS067162,Atypical hypotonia cystinuria syndrome
+BMGC_DS17537,BMG_DS067163,Lethal polymalformative syndrome Boissel type
+BMGC_DS17538,BMG_DS067164,Primary CD59 deficiency
+BMGC_DS17539,BMG_DS067165,Immunodeficiency due to CD25 deficiency
+BMGC_DS17540,BMG_DS067166,FASTKD2-related infantile mitochondrial encephalomyopathy
+BMGC_DS17541,BMG_DS067174,Susceptibility to viral and mycobacterial infection
+BMGC_DS17542,BMG_DS067177,MT-ATP6-related mitochondrial spastic paraplegia
+BMGC_DS17543,BMG_DS067180,Focal palmoplantar keratoderma with joint keratoses
+BMGC_DS17544,BMG_DS067181,COL4A1-related familial vascular leukoencephalopathy
+BMGC_DS17545,BMG_DS067183,Diffuse palmoplantar keratoderma with painful fissures
+BMGC_DS17546,BMG_DS067186,Combined oxidative phosphorylation defect type 14
+BMGC_DS17547,BMG_DS067189,Undifferentiated myeloproliferative disease
+BMGC_DS17548,BMG_DS067190,Isolated ATP synthase deficiency
+BMGC_DS17549,BMG_DS067364,Iodine deficiency
+BMGC_DS17550,BMG_DS067365,Deficiency of interleukin 36 receptor antagonist
+BMGC_DS17551,BMG_DS067368,Diabetic Glomerulosclerosis
+BMGC_DS17552,BMG_DS067373,osteoarthritis susceptibility 5
+BMGC_DS17553,BMG_DS067374,Spondylometaphyseal dysplasia
+BMGC_DS17554,BMG_DS067375,"Scapuloperoneal Myopathy, MYH7-Related"
+BMGC_DS17555,BMG_DS067376,"INTELLECTUAL DISABILITY-HYPOTONIC FACIES SYNDROME, X-LINKED, 1"
+BMGC_DS17556,BMG_DS067380,"EPILEPSY, FAMILIAL TEMPORAL LOBE, 2"
+BMGC_DS17557,BMG_DS067381,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY 1"
+BMGC_DS17558,BMG_DS067382,"DEAFNESS, AUTOSOMAL DOMINANT 37"
+BMGC_DS17559,BMG_DS067384,Arthrosis
+BMGC_DS17560,BMG_DS067385,FETAL AKINESIA DEFORMATION SEQUENCE 2
+BMGC_DS17561,BMG_DS067386,FETAL AKINESIA DEFORMATION SEQUENCE 4
+BMGC_DS17562,BMG_DS067387,"DEAFNESS, AUTOSOMAL RECESSIVE 99"
+BMGC_DS17563,BMG_DS067388,COFFIN-SIRIS SYNDROME 10
+BMGC_DS17564,BMG_DS067389,FETAL AKINESIA DEFORMATION SEQUENCE 3
+BMGC_DS17565,BMG_DS067390,uridine-cytidineuria
+BMGC_DS17566,BMG_DS067391,Aneurysm osteoarthritis syndrome
+BMGC_DS17567,BMG_DS067392,Recessive mitochondrial ataxia syndrome
+BMGC_DS17568,BMG_DS067393,Familial Horizontal Gaze Palsy with Progressive Scoliosis
+BMGC_DS17569,BMG_DS067394,Autosomal recessive brachyolmia
+BMGC_DS17570,BMG_DS067395,recurrent infections-inflammatory syndrome due to zinc metabolism disorder syndrome
+BMGC_DS17571,BMG_DS067398,Muscle-Specific Receptor Tyrosine Kinase Myasthenia Gravis
+BMGC_DS17572,BMG_DS067406,GCGR-related hyperglucagonemia
+BMGC_DS17573,BMG_DS067410,bilateral generalized polymicrogyria
+BMGC_DS17574,BMG_DS067494,Autosomal recessive cerebellar ataxia due to STUB1 deficiency
+BMGC_DS17575,BMG_DS067495,Congenital pontocerebellar hypoplasia type 10
+BMGC_DS17576,BMG_DS067496,"Severe intellectual disability, progressive spastic diplegia syndrome"
+BMGC_DS17577,BMG_DS067497,Autosomal recessive spastic paraplegia type 69
+BMGC_DS17578,BMG_DS067498,Autosomal recessive spastic paraplegia type 71
+BMGC_DS17579,BMG_DS067500,"Intellectual disability, facial dysmorphism syndrome due to SETD5 haploinsufficiency"
+BMGC_DS17580,BMG_DS067501,"Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome"
+BMGC_DS17581,BMG_DS067503,Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons
+BMGC_DS17582,BMG_DS067504,Huntington disease-like syndrome due to C9ORF72 expansions
+BMGC_DS17583,BMG_DS067505,Lipoic acid synthetase deficiency
+BMGC_DS17584,BMG_DS067506,Lipoyl transferase 1 deficiency
+BMGC_DS17585,BMG_DS067507,Autosomal recessive spastic paraplegia type 60
+BMGC_DS17586,BMG_DS067508,Autosomal recessive spastic paraplegia type 66
+BMGC_DS17587,BMG_DS067510,Severe combined immunodeficiency due to IKK2 deficiency
+BMGC_DS17588,BMG_DS067511,"Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome"
+BMGC_DS17589,BMG_DS067512,"Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome"
+BMGC_DS17590,BMG_DS067513,"Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome"
+BMGC_DS17591,BMG_DS067514,"Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome"
+BMGC_DS17592,BMG_DS067517,X-linked dyserythropoietic anemia with abnormal platelets and neutropenia
+BMGC_DS17593,BMG_DS067518,Mitochondrial DNA depletion syndrome hepatocerebrorenal form
+BMGC_DS17594,BMG_DS067519,Congenital muscular dystrophy with intellectual disability and severe epilepsy
+BMGC_DS17595,BMG_DS067520,Lethal arteriopathy syndrome due to fibulin-4 deficiency
+BMGC_DS17596,BMG_DS067523,High bone mass osteogenesis imperfecta
+BMGC_DS17597,BMG_DS067524,Autosomal recessive spondylometaphyseal dysplasia Megarbane type
+BMGC_DS17598,BMG_DS067525,X-linked osteoporosis with fractures
+BMGC_DS17599,BMG_DS067526,X-linked calvarial hyperostosis
+BMGC_DS17600,BMG_DS067529,Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome
+BMGC_DS17601,BMG_DS067530,Sodium channelopathy-related small fiber neuropathy
+BMGC_DS17602,BMG_DS067531,"Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome"
+BMGC_DS17603,BMG_DS067532,Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency
+BMGC_DS17604,BMG_DS067535,Autosomal recessive nail dysplasia
+BMGC_DS17605,BMG_DS067536,Hemoglobinopathy Toms River
+BMGC_DS17606,BMG_DS067537,Hereditary sensorimotor neuropathy with hyperelastic skin
+BMGC_DS17607,BMG_DS067538,Fatal infantile hypertonic myofibrillar myopathy
+BMGC_DS17608,BMG_DS067539,"Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome"
+BMGC_DS17609,BMG_DS067540,Inherited congenital spastic tetraplegia
+BMGC_DS17610,BMG_DS067543,Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
+BMGC_DS17611,BMG_DS067544,Hereditary cryohydrocytosis with reduced stomatin
+BMGC_DS17612,BMG_DS067546,"Brachydactyly, short stature, retinitis pigmentosa syndrome"
+BMGC_DS17613,BMG_DS067564,Recurrent Neisseria infection due to factor D deficiency
+BMGC_DS17614,BMG_DS067571,Progressive myoclonic epilepsy type 5
+BMGC_DS17615,BMG_DS067573,Atypical dentin dysplasia due to SMOC2 deficiency
+BMGC_DS17616,BMG_DS067574,"Autosomal recessive cerebellar ataxia, psychomotor delay syndrome"
+BMGC_DS17617,BMG_DS067575,"Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion"
+BMGC_DS17618,BMG_DS067576,Progressive myoclonic epilepsy type 6
+BMGC_DS17619,BMG_DS067577,Autosomal recessive optic atrophy type 7
+BMGC_DS17620,BMG_DS067578,"Macrocephaly, intellectual disability, autism syndrome"
+BMGC_DS17621,BMG_DS067579,"46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome"
+BMGC_DS17622,BMG_DS067580,"46,XY disorder of sex development, adrenal insufficiency due to CYP11A1 deficiency"
+BMGC_DS17623,BMG_DS067582,Short stature due to partial growth hormone receptor deficiency
+BMGC_DS17624,BMG_DS067583,Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering
+BMGC_DS17625,BMG_DS067586,Progressive myoclonic epilepsy type 8
+BMGC_DS17626,BMG_DS067587,Pancytopenia due to IKZF1 mutations
+BMGC_DS17627,BMG_DS067588,Distal nebulin myopathy
+BMGC_DS17628,BMG_DS067594,Familial dementia British type
+BMGC_DS17629,BMG_DS067597,Congenital muscular dystrophy with intellectual disability
+BMGC_DS17630,BMG_DS067598,Congenital muscular dystrophy without intellectual disability
+BMGC_DS17631,BMG_DS067599,Congenital muscular dystrophy with cerebellar involvement
+BMGC_DS17632,BMG_DS067604,Chronic respiratory distress with surfactant metabolism deficiency
+BMGC_DS17633,BMG_DS067609,Hereditary sensory and autonomic neuropathy due to tectonin beta-propeller repeat containing 2 mutation
+BMGC_DS17634,BMG_DS067610,Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency
+BMGC_DS17635,BMG_DS067611,Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency
+BMGC_DS17636,BMG_DS067612,Autosomal recessive severe congenital neutropenia due to CSF3R deficiency
+BMGC_DS17637,BMG_DS067613,Autosomal dominant secondary polycythemia
+BMGC_DS17638,BMG_DS067619,Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection
+BMGC_DS17639,BMG_DS067620,"Megalocornea, spherophakia, secondary glaucoma syndrome"
+BMGC_DS17640,BMG_DS067623,Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
+BMGC_DS17641,BMG_DS067625,Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome
+BMGC_DS17642,BMG_DS067626,Hereditary isolated aplastic anemia
+BMGC_DS17643,BMG_DS067628,Obesity due to CEP19 deficiency
+BMGC_DS17644,BMG_DS067629,"Ichthyosis, short stature, brachydactyly, microspherophakia syndrome"
+BMGC_DS17645,BMG_DS067630,Autosomal recessive limb girdle muscular dystrophy type 2U
+BMGC_DS17646,BMG_DS067632,Severe early-onset obesity insulin resistance syndrome due to SH2B1 deficiency
+BMGC_DS17647,BMG_DS067633,Combined oxidative phosphorylation defect type 11
+BMGC_DS17648,BMG_DS067638,Familial steroid-resistant nephrotic syndrome with sensorineural deafness
+BMGC_DS17649,BMG_DS067640,Perilipin 1 related familial partial lipodystrophy
+BMGC_DS17650,BMG_DS067641,Severe combined immunodeficiency due to LCK deficiency
+BMGC_DS17651,BMG_DS067642,Lower motor neuron syndrome with late-adult onset
+BMGC_DS17652,BMG_DS067643,DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
+BMGC_DS17653,BMG_DS067644,Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis
+BMGC_DS17654,BMG_DS067645,Immunodeficiency with factor I anomaly
+BMGC_DS17655,BMG_DS067648,X-linked intellectual disability due to GRIA3 mutations
+BMGC_DS17656,BMG_DS067651,Obesity due to SIM1 deficiency
+BMGC_DS17657,BMG_DS067655,"Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency"
+BMGC_DS17658,BMG_DS067658,"Hirschsprung disease, ganglioneuroblastoma syndrome"
+BMGC_DS17659,BMG_DS067659,Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency
+BMGC_DS17660,BMG_DS067660,Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency
+BMGC_DS17661,BMG_DS067661,Combined immunodeficiency with granulomatosis
+BMGC_DS17662,BMG_DS067662,Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene
+BMGC_DS17663,BMG_DS067663,Autosomal recessive hyperinsulinism due to SUR1 deficiency
+BMGC_DS17664,BMG_DS067664,Autosomal recessive hyperinsulinism due to Kir6.2 deficiency
+BMGC_DS17665,BMG_DS067665,Alpha-B crystallin-related late-onset myopathy
+BMGC_DS17666,BMG_DS067670,Combined immunodeficiency due to interleukin 21 receptor deficiency
+BMGC_DS17667,BMG_DS067671,Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
+BMGC_DS17668,BMG_DS067672,Familial congenital mirror movements
+BMGC_DS17669,BMG_DS067674,Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
+BMGC_DS17670,BMG_DS067675,Familial mesial temporal lobe epilepsy with febrile seizures
+BMGC_DS17671,BMG_DS067683,Muscle eye brain disease with bilateral multicystic leukodystrophy
+BMGC_DS17672,BMG_DS067684,"Multiple congenital anomalies, hypotonia, seizures syndrome"
+BMGC_DS17673,BMG_DS067690,Obesity due to leptin receptor gene deficiency
+BMGC_DS17674,BMG_DS067692,"Pyoderma gangrenosum, acne, suppurative hidradenitis syndrome"
+BMGC_DS17675,BMG_DS067693,Hyperekplexia epilepsy syndrome
+BMGC_DS17676,BMG_DS067694,Chronic infantile diarrhea due to guanylate cyclase 2C overactivity
+BMGC_DS17677,BMG_DS067703,Synucleinopathies
+BMGC_DS17678,BMG_DS067762,familial papillary or follicular thyroid carcinoma
+BMGC_DS17679,BMG_DS067813,"Developmental delay, facial dysmorphism syndrome due to MED13L deficiency"
+BMGC_DS17680,BMG_DS067834,21q22.11q22.12 microdeletion syndrome
+BMGC_DS17681,BMG_DS067835,Childhood-onset autosomal recessive myopathy with external ophthalmoplegia
+BMGC_DS17682,BMG_DS067836,"Intellectual disability, hyperkinetic movement, truncal ataxia syndrome"
+BMGC_DS17683,BMG_DS067837,"ANK3-related intellectual disability, sleep disturbance syndrome"
+BMGC_DS17684,BMG_DS067843,Hereditary mixed polyposis syndrome
+BMGC_DS17685,BMG_DS067857,DNA2-related mitochondrial DNA deletion syndrome
+BMGC_DS17686,BMG_DS067858,"ARTHROGRYPOSIS, DISTAL, TYPE 2B4"
+BMGC_DS17687,BMG_DS067859,CALVARIAL DOUGHNUT LESIONS WITH BONE FRAGILITY AND SPONDYLOMETAPHYSEAL DYSPLASIA
+BMGC_DS17688,BMG_DS067860,GIST-PLUS SYNDROME
+BMGC_DS17689,BMG_DS067861,D-LACTIC ACIDURIA WITH GOUT
+BMGC_DS17690,BMG_DS067862,"MITOCHONDRIAL MYOPATHY, EPISODIC, WITH OR WITHOUT OPTIC ATROPHY AND REVERSIBLE LEUKOENCEPHALOPATHY"
+BMGC_DS17691,BMG_DS067863,MULLEGAMA-KLEIN-MARTINEZ SYNDROME
+BMGC_DS17692,BMG_DS067864,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 108"
+BMGC_DS17693,BMG_DS067865,PAGANINI-MIOZZO SYNDROME
+BMGC_DS17694,BMG_DS067866,"NEPHROTIC SYNDROME, TYPE 20"
+BMGC_DS17695,BMG_DS067867,"DEAFNESS, Y-LINKED 2"
+BMGC_DS17696,BMG_DS067868,"ARTHROGRYPOSIS, DISTAL, TYPE 2B1"
+BMGC_DS17697,BMG_DS067869,CONGENITAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE
+BMGC_DS17698,BMG_DS067870,"MICROPHTHALMIA, SYNDROMIC 15"
+BMGC_DS17699,BMG_DS067871,CONE-ROD DYSTROPHY AND HEARING LOSS 1
+BMGC_DS17700,BMG_DS067872,WARBURG-CINOTTI SYNDROME
+BMGC_DS17701,BMG_DS067873,DIAMOND-BLACKFAN ANEMIA 18
+BMGC_DS17702,BMG_DS067874,DIAMOND-BLACKFAN ANEMIA 19
+BMGC_DS17703,BMG_DS067875,DIAMOND-BLACKFAN ANEMIA 20
+BMGC_DS17704,BMG_DS067876,"HYPOMAGNESEMIA, SEIZURES, AND IMPAIRED INTELLECTUAL DEVELOPMENT 2"
+BMGC_DS17705,BMG_DS067877,"TMEM94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome"
+BMGC_DS17706,BMG_DS067878,"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 7, AUTOSOMAL RECESSIVE"
+BMGC_DS17707,BMG_DS067879,NAD(P)HX dehydratase deficiency
+BMGC_DS17708,BMG_DS067880,"MYASTHENIC SYNDROME, CONGENITAL, 25, PRESYNAPTIC"
+BMGC_DS17709,BMG_DS067881,CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION 2
+BMGC_DS17710,BMG_DS067882,LISSENCEPHALY 9 WITH COMPLEX BRAINSTEM MALFORMATION
+BMGC_DS17711,BMG_DS067883,Neonatal epileptic encephalopathy due to glutaminase deficiency
+BMGC_DS17712,BMG_DS067884,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 37
+BMGC_DS17713,BMG_DS067885,GLOBAL DEVELOPMENTAL DELAY WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
+BMGC_DS17714,BMG_DS067886,"ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH EPISODIC RHABDOMYOLYSIS"
+BMGC_DS17715,BMG_DS067887,MENKE-HENNEKAM SYNDROME 1
+BMGC_DS17716,BMG_DS067888,MENKE-HENNEKAM SYNDROME 2
+BMGC_DS17717,BMG_DS067889,"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"
+BMGC_DS17719,BMG_DS067891,SPERMATOGENIC FAILURE 35
+BMGC_DS17720,BMG_DS067892,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH ABNORMAL BEHAVIOR, MICROCEPHALY, AND SHORT STATURE"
+BMGC_DS17721,BMG_DS067893,POLYMICROGYRIA WITH OR WITHOUT VASCULAR-TYPE EHLERS-DANLOS SYNDROME
+BMGC_DS17722,BMG_DS067894,RETINITIS PIGMENTOSA 85
+BMGC_DS17723,BMG_DS067895,"MICROCEPHALY, GROWTH DEFICIENCY, SEIZURES, AND BRAIN MALFORMATIONS"
+BMGC_DS17724,BMG_DS067896,GALLOWAY-MOWAT SYNDROME 6
+BMGC_DS17725,BMG_DS067897,GALLOWAY-MOWAT SYNDROME 7
+BMGC_DS17726,BMG_DS067898,GALLOWAY-MOWAT SYNDROME 8
+BMGC_DS17727,BMG_DS067899,"MICROCEPHALY 25, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS17728,BMG_DS067900,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 6
+BMGC_DS17729,BMG_DS067901,HOUGE-JANSSENS SYNDROME 3
+BMGC_DS17730,BMG_DS067902,NEURODEVELOPMENTAL DISORDER WITH CENTRAL AND PERIPHERAL MOTOR DYSFUNCTION
+BMGC_DS17731,BMG_DS067903,"epilepsy, idiopathic generalized, susceptibility to, 15"
+BMGC_DS17732,BMG_DS067904,CONE-ROD DYSTROPHY AND HEARING LOSS 2
+BMGC_DS17733,BMG_DS067905,BRAIN SMALL VESSEL DISEASE 3
+BMGC_DS17734,BMG_DS067906,COFFIN-SIRIS SYNDROME 8
+BMGC_DS17735,BMG_DS067907,"SHORT STATURE, AMELOGENESIS IMPERFECTA, AND SKELETAL DYSPLASIA WITH SCOLIOSIS"
+BMGC_DS17736,BMG_DS067908,"MYOCLONUS, FAMILIAL, 2"
+BMGC_DS17737,BMG_DS067909,"MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome"
+BMGC_DS17738,BMG_DS067910,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 27"
+BMGC_DS17739,BMG_DS067911,TURNPENNY-FRY SYNDROME
+BMGC_DS17740,BMG_DS067912,"CANCER, ALOPECIA, PIGMENT DYSCRASIA, ONYCHODYSTROPHY, AND KERATODERMA"
+BMGC_DS17741,BMG_DS067913,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 72
+BMGC_DS17742,BMG_DS067914,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 38
+BMGC_DS17743,BMG_DS067915,RNF13-related severe early-onset epileptic encephalopathy
+BMGC_DS17744,BMG_DS067916,"Facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth syndrome"
+BMGC_DS17745,BMG_DS067917,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 69"
+BMGC_DS17746,BMG_DS067918,Acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate
+BMGC_DS17747,BMG_DS067919,"AMELOGENESIS IMPERFECTA, TYPE IIIC"
+BMGC_DS17748,BMG_DS067920,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY 3"
+BMGC_DS17749,BMG_DS067921,"SPONDYLOEPIPHYSEAL DYSPLASIA, KONDO-FU TYPE"
+BMGC_DS17750,BMG_DS067922,IMMUNODEFICIENCY 60 AND AUTOIMMUNITY
+BMGC_DS17751,BMG_DS067923,"Spondyloepimetaphyseal dysplasia with joint laxity, EXOC6B type"
+BMGC_DS17752,BMG_DS067924,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 74
+BMGC_DS17753,BMG_DS067925,Combined oxidative phosphorylation defect type 39
+BMGC_DS17754,BMG_DS067926,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2EE"
+BMGC_DS17755,BMG_DS067927,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 70"
+BMGC_DS17756,BMG_DS067928,"LEUKODYSTROPHY, HYPOMYELINATING, 18"
+BMGC_DS17757,BMG_DS067929,"DEAFNESS, AUTOSOMAL RECESSIVE 113"
+BMGC_DS17758,BMG_DS067930,"GLOBAL DEVELOPMENTAL DELAY, PROGRESSIVE ATAXIA, AND ELEVATED GLUTAMINE"
+BMGC_DS17759,BMG_DS067931,Congenital myopathy with reduced type 2 muscle fibers
+BMGC_DS17760,BMG_DS067932,CATARACT 48
+BMGC_DS17761,BMG_DS067933,"METABOLIC CRISES, RECURRENT, WITH VARIABLE ENCEPHALOMYOPATHIC FEATURES AND NEUROLOGIC REGRESSION"
+BMGC_DS17762,BMG_DS067934,"SPASTIC PARAPLEGIA 80, AUTOSOMAL DOMINANT"
+BMGC_DS17763,BMG_DS067935,MYOECTODERMAL GONADAL DYSGENESIS SYNDROME
+BMGC_DS17764,BMG_DS067936,SPERMATOGENIC FAILURE 36
+BMGC_DS17765,BMG_DS067937,"DEAFNESS, AUTOSOMAL RECESSIVE 100"
+BMGC_DS17766,BMG_DS067938,NEURODEVELOPMENTAL DISORDER WITH IMPAIRED SPEECH AND HYPERKINETIC MOVEMENTS
+BMGC_DS17767,BMG_DS067939,"encephalopathy, acute, infection-induced, susceptibility to, 9"
+BMGC_DS17768,BMG_DS067940,SPERMATOGENIC FAILURE 37
+BMGC_DS17769,BMG_DS067941,DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES
+BMGC_DS17770,BMG_DS067942,"HYDATIDIFORM MOLE, RECURRENT, 3"
+BMGC_DS17771,BMG_DS067943,"HYDATIDIFORM MOLE, RECURRENT, 4"
+BMGC_DS17772,BMG_DS067944,SPERMATOGENIC FAILURE 38
+BMGC_DS17773,BMG_DS067945,"DEAFNESS, AUTOSOMAL RECESSIVE 94"
+BMGC_DS17774,BMG_DS067946,"ARTHROGRYPOSIS, DISTAL, TYPE 2B2"
+BMGC_DS17775,BMG_DS067947,"ARTHROGRYPOSIS, DISTAL, TYPE 2B3"
+BMGC_DS17776,BMG_DS067948,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 75
+BMGC_DS17777,BMG_DS067949,"SPASTIC ATAXIA 9, AUTOSOMAL RECESSIVE"
+BMGC_DS17778,BMG_DS067950,Oculocerebrodental syndrome
+BMGC_DS17779,BMG_DS067951,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT VARIABLE BRAIN ABNORMALITIES
+BMGC_DS17780,BMG_DS067952,"CILIARY DYSKINESIA, PRIMARY, 41"
+BMGC_DS17781,BMG_DS067953,"NEURODEGENERATION, EARLY-ONSET, WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA"
+BMGC_DS17782,BMG_DS067954,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND VARIABLE SKELETAL ANOMALIES
+BMGC_DS17783,BMG_DS067955,DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM
+BMGC_DS17784,BMG_DS067956,"DEAFNESS, AUTOSOMAL RECESSIVE 114"
+BMGC_DS17785,BMG_DS067957,"DEAFNESS, AUTOSOMAL RECESSIVE 115"
+BMGC_DS17786,BMG_DS067958,IMMUNODEFICIENCY 62
+BMGC_DS17787,BMG_DS067959,KHAN-KHAN-KATSANIS SYNDROME
+BMGC_DS17788,BMG_DS067960,"BLEEDING DISORDER, PLATELET-TYPE, 22"
+BMGC_DS17789,BMG_DS067961,PHEOCHROMOCYTOMA/PARAGANGLIOMA SYNDROME 6
+BMGC_DS17790,BMG_DS067962,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 76
+BMGC_DS17791,BMG_DS067963,"CONTRACTURES, PTERYGIA, AND SPONDYLOCARPOTARSAL FUSION SYNDROME 1B"
+BMGC_DS17792,BMG_DS067964,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEVERE SPEECH AND AMBULATION DEFECTS
+BMGC_DS17793,BMG_DS067965,PHEOCHROMOCYTOMA/PARAGANGLIOMA SYNDROME 7
+BMGC_DS17794,BMG_DS067966,"BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS"
+BMGC_DS17795,BMG_DS067967,"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME"
+BMGC_DS17796,BMG_DS067968,NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND SPEECH AND WALKING IMPAIRMENT
+BMGC_DS17797,BMG_DS067969,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 10"
+BMGC_DS17798,BMG_DS067970,"ARTHROGRYPOSIS MULTIPLEX CONGENITA 3, MYOGENIC TYPE"
+BMGC_DS17799,BMG_DS067971,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND STRUCTURAL BRAIN ANOMALIES
+BMGC_DS17800,BMG_DS067972,"HYPOTONIA, HYPOVENTILATION, IMPAIRED INTELLECTUAL DEVELOPMENT, DYSAUTONOMIA, EPILEPSY, AND EYE ABNORMALITIES"
+BMGC_DS17801,BMG_DS067973,"CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES"
+BMGC_DS17802,BMG_DS067974,IMMUNODEFICIENCY 63 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY
+BMGC_DS17803,BMG_DS067975,AORTIC VALVE DISEASE 3
+BMGC_DS17804,BMG_DS067976,NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND NONEPILEPTIC HYPERKINETIC MOVEMENTS
+BMGC_DS17805,BMG_DS067977,"POLYDACTYLY, POSTAXIAL, TYPE A10"
+BMGC_DS17806,BMG_DS067978,NOONAN SYNDROME 11
+BMGC_DS17807,BMG_DS067979,HOLOPROSENCEPHALY 12 WITH OR WITHOUT PANCREATIC AGENESIS
+BMGC_DS17808,BMG_DS067980,CEREBELLAR ATROPHY WITH SEIZURES AND VARIABLE DEVELOPMENTAL DELAY
+BMGC_DS17809,BMG_DS067981,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 71"
+BMGC_DS17810,BMG_DS067982,STOLERMAN NEURODEVELOPMENTAL SYNDROME
+BMGC_DS17811,BMG_DS067983,"NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIC, WITH OPTIC ATROPHY"
+BMGC_DS17812,BMG_DS067984,O'Donnell-Luria-Rodan syndrome
+BMGC_DS17813,BMG_DS067985,LEBER CONGENITAL AMAUROSIS 19
+BMGC_DS17814,BMG_DS067986,"HYPER-IgE SYNDROME 4B, AUTOSOMAL RECESSIVE, WITH RECURRENT INFECTIONS"
+BMGC_DS17815,BMG_DS067987,MITOCHONDRIAL DNA DEPLETION SYNDROME 16 (HEPATIC TYPE)
+BMGC_DS17816,BMG_DS067988,"ROBINOW SYNDROME, AUTOSOMAL RECESSIVE 2"
+BMGC_DS17817,BMG_DS067989,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 6
+BMGC_DS17818,BMG_DS067990,"ECTODERMAL DYSPLASIA 15, HYPOHIDROTIC/HAIR TYPE"
+BMGC_DS17819,BMG_DS067991,SHUKLA-VERNON SYNDROME
+BMGC_DS17820,BMG_DS067992,"ICHTHYOTIC KERATODERMA, SPASTICITY, HYPOMYELINATION, AND DYSMORPHIC FACIAL FEATURES"
+BMGC_DS17821,BMG_DS067993,MICROPHTHALMIA AND/OR COLOBOMA WITH DEVELOPMENTAL DELAY
+BMGC_DS17822,BMG_DS068002,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 59"
+BMGC_DS17823,BMG_DS068011,"MITOCHONDRIAL MYOPATHY, EPISODIC, WITHOUT OPTIC ATROPHY AND REVERSIBLE LEUKOENCEPHALOPATHY"
+BMGC_DS17824,BMG_DS068012,"MITOCHONDRIAL MYOPATHY, EPISODIC, WITH OPTIC ATROPHY AND REVERSIBLE LEUKOENCEPHALOPATHY"
+BMGC_DS17825,BMG_DS068016,"HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHISM"
+BMGC_DS17826,BMG_DS068021,Microcytic anemia
+BMGC_DS17827,BMG_DS068044,X-Linked Familial Exudative Vitreoretinopathy
+BMGC_DS17828,BMG_DS068047,Inherited Immunodeficiency Diseases
+BMGC_DS17829,BMG_DS068050,Evaporative Dry Eye Disease
+BMGC_DS17830,BMG_DS068054,Adenylosuccinate lyase deficiency type 4
+BMGC_DS17831,BMG_DS068055,Adenylosuccinate lyase deficiency type 3
+BMGC_DS17832,BMG_DS068056,Adenylosuccinate lyase deficiency type 2
+BMGC_DS17833,BMG_DS068057,Adenylosuccinate lyase deficiency type 1
+BMGC_DS17834,BMG_DS068058,Autosomal dominant Robinow syndrome
+BMGC_DS17835,BMG_DS068065,Pes Anserine Bursitis
+BMGC_DS17836,BMG_DS068069,"SHORT SLEEP, FAMILIAL NATURAL, 1"
+BMGC_DS17837,BMG_DS068070,Giant Axonal Neuropathy
+BMGC_DS17838,BMG_DS068071,macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
+BMGC_DS17839,BMG_DS068078,Complete achromatopsia
+BMGC_DS17840,BMG_DS068080,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 1
+BMGC_DS17841,BMG_DS068081,Blau syndrome
+BMGC_DS17842,BMG_DS068084,"HYPOPIGMENTATION, ORGANOMEGALY, AND DELAYED MYELINATION AND DEVELOPMENT"
+BMGC_DS17843,BMG_DS068085,"MYOPATHY, DISTAL, 6, ADULT-ONSET, AUTOSOMAL DOMINANT"
+BMGC_DS17844,BMG_DS068086,"ROTHMUND-THOMSON SYNDROME, TYPE 2"
+BMGC_DS17845,BMG_DS068087,"NEUTROPENIA, SEVERE CONGENITAL, 8, AUTOSOMAL DOMINANT"
+BMGC_DS17846,BMG_DS068088,COVID-19 Virus Disease
+BMGC_DS17847,BMG_DS068089,Focal facial dermal dysplasia type III
+BMGC_DS17848,BMG_DS068188,"Blepharophimosis, intellectual disability syndrome"
+BMGC_DS17849,BMG_DS068269,"Primary hyperaldosteronism, seizures, neurological abnormalities syndrome"
+BMGC_DS17850,BMG_DS068303,ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis
+BMGC_DS17851,BMG_DS068334,Trichorhinophalangeal syndrome type 1 and 3
+BMGC_DS17852,BMG_DS068336,posterior hypospadias
+BMGC_DS17853,BMG_DS068339,Generalized glucocorticoid resistance syndrome
+BMGC_DS17854,BMG_DS068347,Palsy of glossopharyngeal nerve
+BMGC_DS17855,BMG_DS068349,Autosomal dominant progressive external ophthalmoplegia
+BMGC_DS17856,BMG_DS068351,X-linked progressive cerebellar ataxia
+BMGC_DS17857,BMG_DS068353,OCULOPHARYNGODISTAL MYOPATHY 1
+BMGC_DS17858,BMG_DS068354,"BLADDER DYSFUNCTION, AUTONOMIC, WITH IMPAIRED PUPILLARY REFLEX AND SECONDARY CAKUT"
+BMGC_DS17859,BMG_DS068355,"CEREBELLAR HYPOPLASIA/ATROPHY, EPILEPSY, AND GLOBAL DEVELOPMENTAL DELAY"
+BMGC_DS17860,BMG_DS068356,"HYDROCEPHALUS, NORMAL-PRESSURE, 1"
+BMGC_DS17861,BMG_DS068357,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Icc"
+BMGC_DS17862,BMG_DS068358,BASILICATA-AKHTAR SYNDROME
+BMGC_DS17863,BMG_DS068359,"HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 8"
+BMGC_DS17864,BMG_DS068360,"HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 9"
+BMGC_DS17865,BMG_DS068361,"CHOLESTASIS, LOW GGT, ACUTE LIVER FAILURE, AND NEURODEGENERATION SYNDROME"
+BMGC_DS17866,BMG_DS068362,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 61"
+BMGC_DS17867,BMG_DS068363,CONGENITAL MYOPATHY 16
+BMGC_DS17868,BMG_DS068364,IMMUNODEFICIENCY 64 WITH LYMPHOPROLIFERATION
+BMGC_DS17869,BMG_DS068365,"TRICHOTHIODYSTROPHY 7, NONPHOTOSENSITIVE"
+BMGC_DS17870,BMG_DS068366,NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES
+BMGC_DS17871,BMG_DS068367,MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 4
+BMGC_DS17872,BMG_DS068368,"hepatitis, fulminant viral, susceptibility to"
+BMGC_DS17873,BMG_DS068369,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 7
+BMGC_DS17874,BMG_DS068370,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE1I"
+BMGC_DS17875,BMG_DS068371,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 78
+BMGC_DS17876,BMG_DS068372,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 79
+BMGC_DS17877,BMG_DS068373,Pontine autosomal dominant microangiopathy with leukoencephalopathy
+BMGC_DS17878,BMG_DS068374,MITOCHONDRIAL DNA DEPLETION SYNDROME 17
+BMGC_DS17879,BMG_DS068375,"NEURODEVELOPMENTAL DISORDER WITH ATAXIA, HYPOTONIA, AND MICROCEPHALY"
+BMGC_DS17880,BMG_DS068376,"NEURODEVELOPMENTAL DISORDER WITH CATARACTS, POOR GROWTH, AND DYSMORPHIC FACIES"
+BMGC_DS17881,BMG_DS068377,NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR HYPOPLASIA AND SPASTICITY
+BMGC_DS17882,BMG_DS068378,NEURODEVELOPMENTAL DISORDER WITH STRUCTURAL BRAIN ANOMALIES AND DYSMORPHIC FACIES
+BMGC_DS17883,BMG_DS068379,CONGENITAL MYOPATHY 19
+BMGC_DS17884,BMG_DS068380,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 80
+BMGC_DS17885,BMG_DS068381,"NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES, SEIZURES, AND SCOLIOSIS"
+BMGC_DS17886,BMG_DS068382,"SHORT SLEEP, FAMILIAL NATURAL, 2"
+BMGC_DS17887,BMG_DS068383,"epilepsy, idiopathic generalized, susceptibility to, 16"
+BMGC_DS17888,BMG_DS068384,"SPASTIC TETRAPLEGIA AND AXIAL HYPOTONIA, PROGRESSIVE"
+BMGC_DS17889,BMG_DS068385,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES
+BMGC_DS17890,BMG_DS068386,SNIJDERS BLOK-FISHER SYNDROME
+BMGC_DS17891,BMG_DS068387,"PONTOCEREBELLAR HYPOPLASIA, TYPE 13"
+BMGC_DS17892,BMG_DS068388,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH NASAL SPEECH, DYSMORPHIC FACIES, AND VARIABLE SKELETAL ANOMALIES"
+BMGC_DS17893,BMG_DS068389,"LOWER URINARY TRACT OBSTRUCTION, CONGENITAL"
+BMGC_DS17894,BMG_DS068390,RETINITIS PIGMENTOSA 86
+BMGC_DS17895,BMG_DS068391,Weiss-Kruszka syndrome
+BMGC_DS17896,BMG_DS068392,ABDOMINAL OBESITY-METABOLIC SYNDROME 4
+BMGC_DS17897,BMG_DS068393,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES"
+BMGC_DS17898,BMG_DS068394,NOONAN SYNDROME 12
+BMGC_DS17899,BMG_DS068395,Rothmund Thomson syndrome type 1
+BMGC_DS17900,BMG_DS068396,"USHER SYNDROME, TYPE 1M"
+BMGC_DS17901,BMG_DS068397,SIDDIQI SYNDROME
+BMGC_DS17902,BMG_DS068398,OCULOPHARYNGEAL MYOPATHY WITH LEUKOENCEPHALOPATHY 1
+BMGC_DS17903,BMG_DS068399,INFANTILE LIVER FAILURE SYNDROME 3
+BMGC_DS17904,BMG_DS068400,SPERMATOGENIC FAILURE 39
+BMGC_DS17905,BMG_DS068401,"OSTEOGENESIS IMPERFECTA, TYPE XX"
+BMGC_DS17906,BMG_DS068402,DIENCEPHALIC-MESENCEPHALIC JUNCTION DYSPLASIA SYNDROME 2
+BMGC_DS17907,BMG_DS068403,"IMMUNODEFICIENCY 65, SUSCEPTIBILITY TO VIRAL INFECTIONS"
+BMGC_DS17908,BMG_DS068404,HALPERIN-BIRK SYNDROME
+BMGC_DS17909,BMG_DS068405,NEUROOCULOCARDIOGENITOURINARY SYNDROME
+BMGC_DS17910,BMG_DS068406,INTELLECTUAL DEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND DYSMORPHIC FACIES
+BMGC_DS17911,BMG_DS068407,CONGENITAL MYOPATHY 8
+BMGC_DS17912,BMG_DS068408,ZIMMERMANN-LABAND SYNDROME 3
+BMGC_DS17913,BMG_DS068409,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES
+BMGC_DS17914,BMG_DS068410,"DIARRHEA 11, MALABSORPTIVE, CONGENITAL"
+BMGC_DS17915,BMG_DS068411,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 81
+BMGC_DS17916,BMG_DS068412,SPERMATOGENIC FAILURE 40
+BMGC_DS17917,BMG_DS068413,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 72"
+BMGC_DS17918,BMG_DS068414,SITOSTEROLEMIA 2
+BMGC_DS17919,BMG_DS068415,"HYDROCEPHALUS, CONGENITAL, 4"
+BMGC_DS17920,BMG_DS068416,SPERMATOGENIC FAILURE 41
+BMGC_DS17921,BMG_DS068417,"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"
+BMGC_DS17923,BMG_DS068419,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 10"
+BMGC_DS17924,BMG_DS068420,"pancreatic cancer, susceptibility to, 5"
+BMGC_DS17925,BMG_DS068421,LESSEL-KUBISCH SYNDROME
+BMGC_DS17926,BMG_DS068422,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 6"
+BMGC_DS17927,BMG_DS068423,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND BEHAVIORAL ABNORMALITIES
+BMGC_DS17928,BMG_DS068424,"LEUKODYSTROPHY, HYPOMYELINATING, 19, TRANSIENT INFANTILE"
+BMGC_DS17929,BMG_DS068425,"ciliary dyskinesia, primary, 42"
+BMGC_DS17930,BMG_DS068426,RETINITIS PIGMENTOSA 87 WITH CHOROIDAL INVOLVEMENT
+BMGC_DS17931,BMG_DS068427,"CILIARY DYSKINESIA, PRIMARY, 43"
+BMGC_DS17932,BMG_DS068428,SHORT STATURE AND MICROCEPHALY WITH GENITAL ANOMALIES
+BMGC_DS17933,BMG_DS068429,NEURODEVELOPMENTAL DISORDER WITH ABSENT LANGUAGE AND VARIABLE SEIZURES
+BMGC_DS17934,BMG_DS068430,NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES
+BMGC_DS17935,BMG_DS068431,"NEURODEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES, ABSENT SPEECH, AND HYPOTONIA"
+BMGC_DS17936,BMG_DS068432,"megabladder, congenital"
+BMGC_DS17937,BMG_DS068433,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 82
+BMGC_DS17938,BMG_DS068434,PREMATURE OVARIAN FAILURE 16
+BMGC_DS17939,BMG_DS068435,HEYN-SPROUL-JACKSON SYNDROME
+BMGC_DS17940,BMG_DS068436,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"
+BMGC_DS17942,BMG_DS068438,"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, ISIDOR-TOUTAIN TYPE"
+BMGC_DS17943,BMG_DS068439,LIANG-WANG SYNDROME
+BMGC_DS17944,BMG_DS068440,"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
+BMGC_DS17946,BMG_DS068442,Poirier-Bienvenu neurodevelopmental syndrome
+BMGC_DS17947,BMG_DS068443,NEUROMUSCULAR OCULOAUDITORY SYNDROME
+BMGC_DS17948,BMG_DS068444,"ANEURYSM, INTRACRANIAL BERRY, 12"
+BMGC_DS17949,BMG_DS068445,STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS
+BMGC_DS17950,BMG_DS068446,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 15"
+BMGC_DS17951,BMG_DS068447,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 83
+BMGC_DS17952,BMG_DS068448,SPERMATOGENIC FAILURE 42
+BMGC_DS17953,BMG_DS068449,INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES
+BMGC_DS17954,BMG_DS068450,SPERMATOGENIC FAILURE 43
+BMGC_DS17955,BMG_DS068451,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS
+BMGC_DS17956,BMG_DS068452,CATIFA SYNDROME
+BMGC_DS17957,BMG_DS068453,JOUBERT SYNDROME 36
+BMGC_DS17958,BMG_DS068454,"ARTHROGRYPOSIS MULTIPLEX CONGENITA 4, NEUROGENIC, WITH AGENESIS OF THE CORPUS CALLOSUM"
+BMGC_DS17959,BMG_DS068455,"CORNEAL DYSTROPHY, MEESMANN, 2"
+BMGC_DS17960,BMG_DS068456,LYMPHATIC MALFORMATION 8
+BMGC_DS17961,BMG_DS068457,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 60, WITH SEIZURES"
+BMGC_DS17962,BMG_DS068458,"NEPHROTIC SYNDROME, TYPE 21"
+BMGC_DS17963,BMG_DS068459,"CORNEAL DYSTROPHY, MEESMANN, 1"
+BMGC_DS17964,BMG_DS068460,CHROMOSOME 12q15 DELETION SYNDROME
+BMGC_DS17965,BMG_DS068468,HEMOLYTIC ANEMIA DUE TO GLUTATHIONE REDUCTASE DEFICIENCY
+BMGC_DS17966,BMG_DS068478,"NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA, SEVERE"
+BMGC_DS17967,BMG_DS068488,"HYPOALPHALIPOPROTEINEMIA, PRIMARY, 1"
+BMGC_DS17968,BMG_DS068490,Secondary Vesicoureteral Reflux
+BMGC_DS17969,BMG_DS068505,Olfactory Impairment
+BMGC_DS17970,BMG_DS068506,Antley-Bixler Syndrome
+BMGC_DS17971,BMG_DS068507,"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA"
+BMGC_DS17972,BMG_DS068509,gastrointestinal defect and immunodeficiency syndrome
+BMGC_DS17973,BMG_DS068512,Hemorrhagic Stroke
+BMGC_DS17974,BMG_DS068516,Acromesomelic dysplasia syndrome
+BMGC_DS17975,BMG_DS068518,Cryptococcosis
+BMGC_DS17976,BMG_DS068519,hereditary spastic paraplegia 30
+BMGC_DS17977,BMG_DS068520,"Neutropenia, Severe Congenital, Autosomal Recessive 3"
+BMGC_DS17978,BMG_DS068525,Focal facial dermal dysplasia type I
+BMGC_DS17979,BMG_DS068526,Hereditary sensory autonomic neuropathy type IA
+BMGC_DS17980,BMG_DS068535,COFFIN-SIRIS SYNDROME 11
+BMGC_DS17981,BMG_DS068536,"HYPOPARATHYROIDISM, FAMILIAL ISOLATED, 1"
+BMGC_DS17982,BMG_DS068537,"radioulnar synostosis, nonsyndromic, susceptibility to"
+BMGC_DS17983,BMG_DS068539,Emery-Dreifuss Muscular Dystrophy 1
+BMGC_DS17984,BMG_DS068540,Cardiometabolic Syndrome
+BMGC_DS17985,BMG_DS068542,Special AT-rich sequence-binding protein 2-associated syndrome
+BMGC_DS17986,BMG_DS068548,acid sphingomyelinase deficiency
+BMGC_DS17987,BMG_DS068550,"Autoimmune interstitial lung disease, arthritis syndrome"
+BMGC_DS17988,BMG_DS068551,cerebral creatine deficiency syndrome
+BMGC_DS17989,BMG_DS068552,Pneumonia caused by SARS-CoV-2
+BMGC_DS17990,BMG_DS068772,Laminopathies
+BMGC_DS17991,BMG_DS068773,Cryptogenic Ischemic Stroke
+BMGC_DS17992,BMG_DS068774,Intracerebral Hemorrhagic Stroke
+BMGC_DS17993,BMG_DS068781,"Respiratory Distress Syndrome, Pediatric"
+BMGC_DS17994,BMG_DS068792,Wake-up Stroke
+BMGC_DS17995,BMG_DS068793,Acute Ischemic Stroke
+BMGC_DS17996,BMG_DS068795,Subarachnoid Hemorrhagic Stroke
+BMGC_DS17997,BMG_DS068805,Smell Dysfunction
+BMGC_DS17998,BMG_DS068814,Taste Dysfunction
+BMGC_DS17999,BMG_DS068815,Pityriasis Folliculitis
+BMGC_DS18000,BMG_DS068819,SILVER-RUSSELL SYNDROME 1
+BMGC_DS18001,BMG_DS068822,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE"
+BMGC_DS18002,BMG_DS068823,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE"
+BMGC_DS18003,BMG_DS068824,"WIEACKER-WOLFF SYNDROME, FEMALE-RESTRICTED"
+BMGC_DS18004,BMG_DS068825,"HOLOPROSENCEPHALY 13, X-LINKED"
+BMGC_DS18005,BMG_DS068826,microform holoprosencephaly
+BMGC_DS18006,BMG_DS068827,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 85 WITH OR WITHOUT MIDLINE BRAIN DEFECTS
+BMGC_DS18007,BMG_DS068828,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIr"
+BMGC_DS18008,BMG_DS068829,"DIABETES MELLITUS, PERMANENT NEONATAL, 1"
+BMGC_DS18009,BMG_DS068831,"intellectual disability, autosomal dominant 9"
+BMGC_DS18010,BMG_DS068832,HAO-FOUNTAIN SYNDROME
+BMGC_DS18011,BMG_DS068833,"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, SPASTICITY, AND BRAIN ATROPHY"
+BMGC_DS18012,BMG_DS068834,"SPASTIC PARAPLEGIA 81, AUTOSOMAL RECESSIVE"
+BMGC_DS18013,BMG_DS068835,"SPASTIC PARAPLEGIA 82, AUTOSOMAL RECESSIVE"
+BMGC_DS18014,BMG_DS068836,CEBALID SYNDROME
+BMGC_DS18015,BMG_DS068837,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 10"
+BMGC_DS18016,BMG_DS068838,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 34"
+BMGC_DS18017,BMG_DS068839,"DEAFNESS, AUTOSOMAL DOMINANT 75"
+BMGC_DS18018,BMG_DS068840,"congenital heart defects, multiple types, 7"
+BMGC_DS18019,BMG_DS068841,"CILIARY DYSKINESIA, PRIMARY, 44"
+BMGC_DS18020,BMG_DS068842,LONG QT SYNDROME 16
+BMGC_DS18021,BMG_DS068843,"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 6"
+BMGC_DS18022,BMG_DS068844,IMAGAWA-MATSUMOTO SYNDROME
+BMGC_DS18023,BMG_DS068845,"DEAFNESS, AUTOSOMAL DOMINANT 76"
+BMGC_DS18024,BMG_DS068846,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 84
+BMGC_DS18025,BMG_DS068847,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62"
+BMGC_DS18026,BMG_DS068848,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEONATAL RESPIRATORY INSUFFICIENCY, AND THERMODYSREGULATION"
+BMGC_DS18027,BMG_DS068849,BECK-FAHRNER SYNDROME
+BMGC_DS18028,BMG_DS068850,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 28"
+BMGC_DS18029,BMG_DS068851,"CILIARY DYSKINESIA, PRIMARY, 45"
+BMGC_DS18030,BMG_DS068852,"RESPIRATORY PAPILLOMATOSIS, JUVENILE RECURRENT, CONGENITAL"
+BMGC_DS18031,BMG_DS068853,SANDESTIG-STEFANOVA SYNDROME
+BMGC_DS18032,BMG_DS068854,TRIOKINASE AND FMN CYCLASE DEFICIENCY SYNDROME
+BMGC_DS18033,BMG_DS068855,"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
+BMGC_DS18035,BMG_DS068857,"PONTOCEREBELLAR HYPOPLASIA, HYPOTONIA, AND RESPIRATORY INSUFFICIENCY SYNDROME, NEONATAL LETHAL"
+BMGC_DS18036,BMG_DS068858,MITOCHONDRIAL DNA DEPLETION SYNDROME 18
+BMGC_DS18037,BMG_DS068859,"CHROMOSOME 1p36.33 DUPLICATION SYNDROME, ATAD3 GENE CLUSTER, AUTOSOMAL DOMINANT"
+BMGC_DS18038,BMG_DS068860,GENITOURINARY AND/OR BRAIN MALFORMATION SYNDROME
+BMGC_DS18039,BMG_DS068861,RHIZOMELIC LIMB SHORTENING WITH DYSMORPHIC FEATURES
+BMGC_DS18040,BMG_DS068862,CONGENITAL MYOPATHY 9A
+BMGC_DS18041,BMG_DS068863,"CONGENITAL MYOPATHY 9B, PROXIMAL, WITH MINICORE LESIONS"
+BMGC_DS18042,BMG_DS068864,"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 8, AUTOSOMAL RECESSIVE"
+BMGC_DS18043,BMG_DS068865,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 63, WITH MACROCEPHALY"
+BMGC_DS18044,BMG_DS068866,RETINITIS PIGMENTOSA 88
+BMGC_DS18045,BMG_DS068867,"MYOPIA 27, AUTOSOMAL DOMINANT"
+BMGC_DS18046,BMG_DS068868,"NABAIS SA-DE VRIES SYNDROME, TYPE 1"
+BMGC_DS18047,BMG_DS068869,"NABAIS SA-DE VRIES SYNDROME, TYPE 2"
+BMGC_DS18048,BMG_DS068870,"autism, susceptibility to, 20"
+BMGC_DS18049,BMG_DS068871,QRSL1-related combined oxidative phosphorylation defect
+BMGC_DS18050,BMG_DS068872,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 41
+BMGC_DS18051,BMG_DS068873,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 42
+BMGC_DS18052,BMG_DS068874,ALOPECIA-INTELLECTUAL DISABILITY SYNDROME 4
+BMGC_DS18053,BMG_DS068875,HYPOGONADOTROPIC HYPOGONADISM 25 WITH ANOSMIA
+BMGC_DS18054,BMG_DS068876,"VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 3"
+BMGC_DS18055,BMG_DS068877,DIETS-JONGMANS SYNDROME
+BMGC_DS18056,BMG_DS068878,IMMUNODEFICIENCY 66
+BMGC_DS18057,BMG_DS068879,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 26"
+BMGC_DS18058,BMG_DS068880,BONE MARROW FAILURE SYNDROME 6
+BMGC_DS18059,BMG_DS068881,HYPERVALINEMIA AND HYPERLEUCINE-ISOLEUCINEMIA
+BMGC_DS18060,BMG_DS068882,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 43
+BMGC_DS18061,BMG_DS068883,autoinflammation with episodic fever and lymphadenopathy
+BMGC_DS18062,BMG_DS068884,ANAUXETIC DYSPLASIA 3
+BMGC_DS18063,BMG_DS068885,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 44
+BMGC_DS18064,BMG_DS068886,"DIABETES MELLITUS, PERMANENT NEONATAL, 2"
+BMGC_DS18065,BMG_DS068887,"DIABETES MELLITUS, PERMANENT NEONATAL, 3"
+BMGC_DS18066,BMG_DS068888,"DEVELOPMENTAL DELAY, EPILEPSY, AND NEONATAL DIABETES 2"
+BMGC_DS18067,BMG_DS068889,"DIABETES MELLITUS, PERMANENT NEONATAL, 4"
+BMGC_DS18068,BMG_DS068890,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISTIC FEATURES AND/OR STRUCTURAL BRAIN ABNORMALITIES
+BMGC_DS18069,BMG_DS068891,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, MICROCEPHALY, AND SEIZURES"
+BMGC_DS18070,BMG_DS068892,RETINAL DYSTROPHY WITH LEUKODYSTROPHY
+BMGC_DS18071,BMG_DS068893,"TREMOR, HEREDITARY ESSENTIAL, 6"
+BMGC_DS18072,BMG_DS068894,"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"
+BMGC_DS18074,BMG_DS068896,NIZON-ISIDOR SYNDROME
+BMGC_DS18075,BMG_DS068897,LISSENCEPHALY 10
+BMGC_DS18076,BMG_DS068898,"SEIZURES, EARLY-ONSET, WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS"
+BMGC_DS18077,BMG_DS068899,"EPILEPSY, PROGRESSIVE MYOCLONIC, 11"
+BMGC_DS18078,BMG_DS068900,"LEUKOENCEPHALOPATHY, DEVELOPMENTAL DELAY, AND EPISODIC NEUROLOGIC REGRESSION SYNDROME"
+BMGC_DS18079,BMG_DS068901,"LEUKOENCEPHALOPATHY, MOTOR DELAY, SPASTICITY, AND DYSARTHRIA SYNDROME"
+BMGC_DS18080,BMG_DS068902,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CEREBELLAR ATROPHY, WITH OR WITHOUT SEIZURES"
+BMGC_DS18081,BMG_DS068903,"GLAUCOMA, PRIMARY CLOSED-ANGLE"
+BMGC_DS18082,BMG_DS068904,Deficiency of galactose mutarotase
+BMGC_DS18083,BMG_DS068905,"HYPOPARATHYROIDISM, FAMILIAL ISOLATED, 2"
+BMGC_DS18084,BMG_DS068906,"proteinuria, chronic benign"
+BMGC_DS18085,BMG_DS068907,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIt"
+BMGC_DS18086,BMG_DS068908,PSEUDO-TORCH SYNDROME 3
+BMGC_DS18087,BMG_DS068910,"Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome"
+BMGC_DS18088,BMG_DS068911,NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY
+BMGC_DS18089,BMG_DS068912,"MICROCEPHALY, DEVELOPMENTAL DELAY, AND BRITTLE HAIR SYNDROME"
+BMGC_DS18090,BMG_DS068913,"46,XX SEX REVERSAL 5"
+BMGC_DS18091,BMG_DS068914,SILVER-RUSSELL SYNDROME 2
+BMGC_DS18092,BMG_DS068915,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES"
+BMGC_DS18093,BMG_DS068916,SILVER-RUSSELL SYNDROME 4
+BMGC_DS18094,BMG_DS068917,SILVER-RUSSELL SYNDROME 5
+BMGC_DS18095,BMG_DS068918,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 86
+BMGC_DS18096,BMG_DS068919,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL RECESSIVE 8"
+BMGC_DS18097,BMG_DS068920,FANCONI RENOTUBULAR SYNDROME 5
+BMGC_DS18098,BMG_DS068921,"NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME"
+BMGC_DS18099,BMG_DS068922,"DEAFNESS, AUTOSOMAL DOMINANT 77"
+BMGC_DS18100,BMG_DS068923,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 87
+BMGC_DS18101,BMG_DS068924,NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND BEHAVIORAL ABNORMALITIES
+BMGC_DS18102,BMG_DS068925,PERIVENTRICULAR NODULAR HETEROTOPIA 9
+BMGC_DS18103,BMG_DS068926,"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 14"
+BMGC_DS18104,BMG_DS068927,"NEURODEVELOPMENTAL DISORDER WITH SEIZURES, HYPOTONIA, AND BRAIN IMAGING ABNORMALITIES"
+BMGC_DS18105,BMG_DS068928,"EPISODIC ATAXIA, TYPE 9"
+BMGC_DS18106,BMG_DS068929,"AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME"
+BMGC_DS18107,BMG_DS068930,"GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 5"
+BMGC_DS18108,BMG_DS068931,TREACHER COLLINS SYNDROME 4
+BMGC_DS18109,BMG_DS068932,oculopharyngodistal myopathy 2
+BMGC_DS18110,BMG_DS068933,"HYPER-IgE SYNDROME 5, AUTOSOMAL RECESSIVE, WITH RECURRENT INFECTIONS"
+BMGC_DS18111,BMG_DS068934,"HETEROTAXY, VISCERAL, 9, AUTOSOMAL, WITH MALE INFERTILITY"
+BMGC_DS18112,BMG_DS068935,RETINITIS PIGMENTOSA 89
+BMGC_DS18113,BMG_DS068936,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 88
+BMGC_DS18114,BMG_DS068937,Mitchell syndrome
+BMGC_DS18115,BMG_DS068938,"Spondylometaphyseal dysplasia, corneal dystrophy syndrome"
+BMGC_DS18116,BMG_DS068968,"CHROMOSOME 1p36.33 DELETION SYNDROME, ATAD3 GENE CLUSTER, AUTOSOMAL RECESSIVE"
+BMGC_DS18117,BMG_DS068969,"DEVELOPMENTAL DELAY, EPILEPSY, AND NEONATAL DIABETES 1"
+BMGC_DS18118,BMG_DS068972,Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis
+BMGC_DS18119,BMG_DS069019,acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
+BMGC_DS18120,BMG_DS069445,Pelizaeus Merzbacher like disease due to AIMP1 mutation
+BMGC_DS18121,BMG_DS069651,Cerebro-oculo-facio-skeletal syndrome
+BMGC_DS18122,BMG_DS069652,FG syndrome 1
+BMGC_DS18123,BMG_DS069653,mismatch repair cancer syndrome 1
+BMGC_DS18124,BMG_DS069656,Mandibuloacral dysplasia with type A lipodystrophy
+BMGC_DS18125,BMG_DS069659,"LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1"
+BMGC_DS18126,BMG_DS069660,"Familial Mediterranean Fever, Autosomal Recessive"
+BMGC_DS18127,BMG_DS069661,Sugarman brachydactyly
+BMGC_DS18128,BMG_DS069662,X-linked scapuloperoneal muscular dystrophy
+BMGC_DS18129,BMG_DS069664,Brachyolmia Type 2
+BMGC_DS18130,BMG_DS069665,gallbladder papillary carcinoma
+BMGC_DS18131,BMG_DS069666,FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1
+BMGC_DS18132,BMG_DS069667,"IFAP SYNDROME 1, WITH OR WITHOUT BRESHECK SYNDROME"
+BMGC_DS18133,BMG_DS069668,Periventricular heterotopia
+BMGC_DS18134,BMG_DS069669,"ROBINOW SYNDROME, AUTOSOMAL RECESSIVE 1"
+BMGC_DS18135,BMG_DS069670,"MYOPATHY, DISTAL, WITH RIMMED VACUOLES"
+BMGC_DS18136,BMG_DS069671,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 2"
+BMGC_DS18137,BMG_DS069672,"RENAL TUBULAR ACIDOSIS, DISTAL, 3, WITH OR WITHOUT SENSORINEURAL HEARING LOSS"
+BMGC_DS18138,BMG_DS069680,pulmonary alveolar proteinosis
+BMGC_DS18139,BMG_DS069683,17q11 deletion syndrome
+BMGC_DS18140,BMG_DS069688,parapharyngeal meningioma
+BMGC_DS18141,BMG_DS069704,OPTIC ATROPHY 13 WITH RETINAL AND FOVEAL ABNORMALITIES
+BMGC_DS18142,BMG_DS069705,"MICROCORNEA, ROD-CONE DYSTROPHY, CATARACT, AND POSTERIOR STAPHYLOMA 2"
+BMGC_DS18143,BMG_DS069706,"ARTHROGRYPOSIS MULTIPLEX CONGENITA 2, NEUROGENIC TYPE"
+BMGC_DS18144,BMG_DS069707,COACH SYNDROME 1
+BMGC_DS18145,BMG_DS069708,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 1"
+BMGC_DS18146,BMG_DS069709,TYPE 1 DIABETES MELLITUS 1
+BMGC_DS18147,BMG_DS069710,PALLISTER-HALL-LIKE SYNDROME
+BMGC_DS18148,BMG_DS069711,"GROWTH HORMONE INSENSITIVITY SYNDROME WITH IMMUNE DYSREGULATION 1, AUTOSOMAL RECESSIVE"
+BMGC_DS18149,BMG_DS069712,"IMMUNODEFICIENCY 74, COVID19-RELATED, X-LINKED"
+BMGC_DS18150,BMG_DS069713,VEXAS syndrome
+BMGC_DS18151,BMG_DS069714,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, MITOCHONDRIAL FORM, 1"
+BMGC_DS18152,BMG_DS069716,"46,XY GONADAL DYSGENESIS WITH MINIFASCICULAR NEUROPATHY"
+BMGC_DS18153,BMG_DS069718,"RENAL TUBULAR ACIDOSIS, DISTAL, 4, WITH HEMOLYTIC ANEMIA"
+BMGC_DS18154,BMG_DS069719,RAJAB INTERSTITIAL LUNG DISEASE WITH BRAIN CALCIFICATIONS 1
+BMGC_DS18155,BMG_DS069720,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 6
+BMGC_DS18156,BMG_DS069721,"MENTAL RETARDATION, AUTOSOMAL DOMINANT 25, FORMERLY"
+BMGC_DS18157,BMG_DS069722,ARTHROGRYPOSIS MULTIPLEX CONGENITA 5
+BMGC_DS18158,BMG_DS069723,SULEIMAN-EL-HATTAB SYNDROME
+BMGC_DS18159,BMG_DS069724,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 45
+BMGC_DS18160,BMG_DS069725,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 46
+BMGC_DS18161,BMG_DS069726,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 47
+BMGC_DS18162,BMG_DS069727,IMMUNODEFICIENCY 69
+BMGC_DS18163,BMG_DS069728,IMMUNODEFICIENCY 70
+BMGC_DS18164,BMG_DS069729,"CONE-ROD SYNAPTIC DISORDER SYNDROME, CONGENITAL NONPROGRESSIVE"
+BMGC_DS18165,BMG_DS069730,TOLCHIN-LE CAIGNEC SYNDROME
+BMGC_DS18166,BMG_DS069731,MITOCHONDRIAL DNA DEPLETION SYNDROME 19
+BMGC_DS18167,BMG_DS069732,SODIUM-DEPENDENT MULTIVITAMIN TRANSPORTER DEFICIENCY
+BMGC_DS18168,BMG_DS069733,LI-GHORBANI-WEISZ-HUBSHMAN SYNDROME
+BMGC_DS18169,BMG_DS069734,"MYOPATHY, CONGENITAL, WITH DIAPHRAGMATIC DEFECTS, RESPIRATORY INSUFFICIENCY, AND DYSMORPHIC FACIES"
+BMGC_DS18170,BMG_DS069735,OPTIC ATROPHY 12
+BMGC_DS18171,BMG_DS069736,IMMUNODEFICIENCY 72 WITH AUTOINFLAMMATION AND LYMPHOPROLIFERATION
+BMGC_DS18172,BMG_DS069737,"GROWTH HORMONE INSENSITIVITY SYNDROME WITH IMMUNE DYSREGULATION 2, AUTOSOMAL DOMINANT"
+BMGC_DS18173,BMG_DS069738,IMMUNODEFICIENCY 73B WITH DEFECTIVE NEUTROPHIL CHEMOTAXIS AND LYMPHOPENIA
+BMGC_DS18174,BMG_DS069739,IMMUNODEFICIENCY 73C WITH DEFECTIVE NEUTROPHIL CHEMOTAXIS AND HYPOGAMMAGLOBULINEMIA
+BMGC_DS18175,BMG_DS069740,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 15"
+BMGC_DS18176,BMG_DS069741,IMMUNE DYSREGULATION AND SYSTEMIC HYPERINFLAMMATION SYNDROME
+BMGC_DS18177,BMG_DS069742,"AUTOINFLAMMATION, IMMUNE DYSREGULATION, AND EOSINOPHILIA"
+BMGC_DS18178,BMG_DS069743,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEIZURES AND LANGUAGE DELAY
+BMGC_DS18179,BMG_DS069744,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 35"
+BMGC_DS18180,BMG_DS069745,DEEAH SYNDROME
+BMGC_DS18181,BMG_DS069746,"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA"
+BMGC_DS18182,BMG_DS069747,RETINITIS PIGMENTOSA 90
+BMGC_DS18183,BMG_DS069748,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 8
+BMGC_DS18184,BMG_DS069749,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 9
+BMGC_DS18185,BMG_DS069750,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 48
+BMGC_DS18186,BMG_DS069751,RAJAB INTERSTITIAL LUNG DISEASE WITH BRAIN CALCIFICATIONS 2
+BMGC_DS18187,BMG_DS069752,IFAP SYNDROME 2
+BMGC_DS18188,BMG_DS069753,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 49
+BMGC_DS18189,BMG_DS069754,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 50
+BMGC_DS18190,BMG_DS069755,NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE SPASTICITY AND BRAIN WHITE MATTER ABNORMALITIES
+BMGC_DS18191,BMG_DS069756,"SPASTIC PARAPLEGIA 83, AUTOSOMAL RECESSIVE"
+BMGC_DS18192,BMG_DS069757,"COENZYME Q10 DEFICIENCY, PRIMARY, 9"
+BMGC_DS18193,BMG_DS069758,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH EPILEPSY, BEHAVIORAL ABNORMALITIES, AND COARSE FACIES"
+BMGC_DS18194,BMG_DS069759,VISSERS-BODMER SYNDROME
+BMGC_DS18195,BMG_DS069760,"MYOPATHY, EPILEPSY, AND PROGRESSIVE CEREBRAL ATROPHY"
+BMGC_DS18196,BMG_DS069761,MYOFIBRILLAR MYOPATHY 10
+BMGC_DS18197,BMG_DS069762,MONOSOMY 7 MYELODYSPLASIA AND LEUKEMIA SYNDROME 2
+BMGC_DS18198,BMG_DS069763,"SPINAL MUSCULAR ATROPHY, INFANTILE, JAMES TYPE"
+BMGC_DS18199,BMG_DS069764,SPERMATOGENIC FAILURE 44
+BMGC_DS18200,BMG_DS069765,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 3"
+BMGC_DS18201,BMG_DS069766,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 4"
+BMGC_DS18202,BMG_DS069767,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 7"
+BMGC_DS18203,BMG_DS069768,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 8"
+BMGC_DS18204,BMG_DS069769,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 10"
+BMGC_DS18205,BMG_DS069770,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 11"
+BMGC_DS18206,BMG_DS069771,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 12"
+BMGC_DS18207,BMG_DS069772,NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES
+BMGC_DS18208,BMG_DS069773,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 51
+BMGC_DS18209,BMG_DS069774,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 14"
+BMGC_DS18210,BMG_DS069775,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 15"
+BMGC_DS18211,BMG_DS069776,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 16"
+BMGC_DS18212,BMG_DS069777,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 17"
+BMGC_DS18213,BMG_DS069778,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 18"
+BMGC_DS18214,BMG_DS069779,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 19"
+BMGC_DS18215,BMG_DS069780,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 20"
+BMGC_DS18216,BMG_DS069781,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 21"
+BMGC_DS18217,BMG_DS069782,"LEUKODYSTROPHY, HYPOMYELINATING, 20"
+BMGC_DS18218,BMG_DS069783,NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ATROPHY
+BMGC_DS18219,BMG_DS069784,"VITAMIN D-DEPENDENT RICKETS, TYPE 3"
+BMGC_DS18220,BMG_DS069785,"CLEFT PALATE, PROLIFERATIVE RETINOPATHY, AND DEVELOPMENTAL DELAY"
+BMGC_DS18221,BMG_DS069786,"Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome"
+BMGC_DS18222,BMG_DS069787,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND BRAIN ATROPHY"
+BMGC_DS18223,BMG_DS069788,INFLAMMATORY BOWEL DISEASE (CROHN DISEASE) 30
+BMGC_DS18224,BMG_DS069789,KILQUIST SYNDROME
+BMGC_DS18225,BMG_DS069790,"DEAFNESS, AUTOSOMAL DOMINANT 78"
+BMGC_DS18226,BMG_DS069791,"MICROCORNEA, ROD-CONE DYSTROPHY, CATARACT, AND POSTERIOR STAPHYLOMA 1"
+BMGC_DS18227,BMG_DS069792,DELPIRE-MCNEILL SYNDROME
+BMGC_DS18228,BMG_DS069793,"DEAFNESS, AUTOSOMAL DOMINANT 79"
+BMGC_DS18229,BMG_DS069794,NOONAN SYNDROME 13
+BMGC_DS18230,BMG_DS069795,"DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY"
+BMGC_DS18231,BMG_DS069796,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, IMPAIRED LANGUAGE, AND GAIT ABNORMALITIES"
+BMGC_DS18232,BMG_DS069797,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, IMPAIRED LANGUAGE, EPILEPSY, AND GAIT ABNORMALITIES"
+BMGC_DS18233,BMG_DS069798,"DEAFNESS, AUTOSOMAL RECESSIVE 116"
+BMGC_DS18234,BMG_DS069799,SPERMATOGENIC FAILURE 45
+BMGC_DS18235,BMG_DS069800,SPERMATOGENIC FAILURE 46
+BMGC_DS18236,BMG_DS069801,mismatch repair cancer syndrome 2
+BMGC_DS18237,BMG_DS069802,mismatch repair cancer syndrome 3
+BMGC_DS18238,BMG_DS069803,INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY AND AXONAL PERIPHERAL NEUROPATHY
+BMGC_DS18239,BMG_DS069804,mismatch repair cancer syndrome 4
+BMGC_DS18240,BMG_DS069805,SPERMATOGENIC FAILURE 47
+BMGC_DS18241,BMG_DS069806,"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES"
+BMGC_DS18242,BMG_DS069807,SPERMATOGENIC FAILURE 48
+BMGC_DS18243,BMG_DS069808,"ARTHROGRYPOSIS, DISTAL, TYPE 1C"
+BMGC_DS18244,BMG_DS069809,COACH SYNDROME 2
+BMGC_DS18245,BMG_DS069810,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 13"
+BMGC_DS18246,BMG_DS069811,COACH SYNDROME 3
+BMGC_DS18247,BMG_DS069812,COMBINED OSTEOGENESIS IMPERFECTA AND EHLERS-DANLOS SYNDROME 1
+BMGC_DS18248,BMG_DS069813,COMBINED OSTEOGENESIS IMPERFECTA AND EHLERS-DANLOS SYNDROME 2
+BMGC_DS18249,BMG_DS069814,"NEURODEVELOPMENTAL DISORDER WITH CARDIOMYOPATHY, SPASTICITY, AND BRAIN ABNORMALITIES"
+BMGC_DS18250,BMG_DS069815,VERTEBRAL HYPERSEGMENTATION AND OROFACIAL ANOMALIES
+BMGC_DS18251,BMG_DS069816,CARDIOFACIONEURODEVELOPMENTAL SYNDROME
+BMGC_DS18252,BMG_DS069817,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 89
+BMGC_DS18253,BMG_DS069818,KAYA-BARAKAT-MASSON SYNDROME
+BMGC_DS18254,BMG_DS069819,IMMUNODEFICIENCY 75 WITH LYMPHOPROLIFERATION
+BMGC_DS18255,BMG_DS069820,MANDIBULOACRAL DYSPLASIA PROGEROID SYNDROME
+BMGC_DS18256,BMG_DS069821,THROMBOCYTOPENIA 7
+BMGC_DS18257,BMG_DS069822,"OSTEOGENESIS IMPERFECTA, TYPE XXI"
+BMGC_DS18258,BMG_DS069823,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 8
+BMGC_DS18259,BMG_DS069824,AMYOTROPHIC LATERAL SCLEROSIS 26 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA
+BMGC_DS18260,BMG_DS069825,RITSCHER-SCHINZEL SYNDROME 3
+BMGC_DS18261,BMG_DS069826,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 5
+BMGC_DS18262,BMG_DS069827,CARDIOACROFACIAL DYSPLASIA 1
+BMGC_DS18263,BMG_DS069828,CARDIOACROFACIAL DYSPLASIA 2
+BMGC_DS18264,BMG_DS069829,SPERMATOGENIC FAILURE 49
+BMGC_DS18265,BMG_DS069830,SPERMATOGENIC FAILURE 50
+BMGC_DS18266,BMG_DS069831,PREMATURE OVARIAN FAILURE 17
+BMGC_DS18267,BMG_DS069832,CHROMOSOME 13q33-q34 DELETION SYNDROME
+BMGC_DS18268,BMG_DS069833,LESSEL-KREIENKAMP SYNDROME
+BMGC_DS18269,BMG_DS069834,INTELLECTUAL DEVELOPMENTAL DISORDER WITH PAROXYSMAL DYSKINESIA OR SEIZURES
+BMGC_DS18270,BMG_DS069836,AMeD syndrome
+BMGC_DS18271,BMG_DS069837,"NEPHROTIC SYNDROME, TYPE 22"
+BMGC_DS18272,BMG_DS069838,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT EARLY-ONSET GENERALIZED EPILEPSY
+BMGC_DS18273,BMG_DS069839,CARPAL TUNNEL SYNDROME 2
+BMGC_DS18274,BMG_DS069840,Oculocutaneous albinism type 8
+BMGC_DS18275,BMG_DS069841,"MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 2"
+BMGC_DS18276,BMG_DS069842,"MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 3"
+BMGC_DS18277,BMG_DS069843,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 36"
+BMGC_DS18278,BMG_DS069844,HERMANSKY-PUDLAK SYNDROME 11
+BMGC_DS18279,BMG_DS069845,"DEAFNESS, AUTOSOMAL RECESSIVE 117"
+BMGC_DS18280,BMG_DS069846,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 10
+BMGC_DS18281,BMG_DS069861,"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 1"
+BMGC_DS18282,BMG_DS069995,Alpha-N-acetylgalactosaminidase deficiency type 3
+BMGC_DS18283,BMG_DS070023,Contact dermatitis caused by urushiol from poison oak
+BMGC_DS18284,BMG_DS070042,Blepharophimosis epicanthus inversus ptosis syndrome plus
+BMGC_DS18285,BMG_DS070045,"malignant hyperthermia, susceptibility to"
+BMGC_DS18286,BMG_DS070052,Mowat-Wilson syndrome due to monosomy 2q22
+BMGC_DS18287,BMG_DS070067,Autosomal recessive epidermolytic ichthyosis
+BMGC_DS18288,BMG_DS070144,complete cryptophthalmia
+BMGC_DS18289,BMG_DS070240,6q16 microdeletion syndrome
+BMGC_DS18290,BMG_DS070248,Pfeiffer syndrome type 1
+BMGC_DS18291,BMG_DS070249,Pelizaeus-Merzbacher disease in female carrier
+BMGC_DS18292,BMG_DS070250,Pfeiffer syndrome type 2
+BMGC_DS18293,BMG_DS070251,Pfeiffer syndrome type 3
+BMGC_DS18294,BMG_DS070281,Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation
+BMGC_DS18295,BMG_DS070282,Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation
+BMGC_DS18296,BMG_DS070333,Stickler syndrome type 4
+BMGC_DS18297,BMG_DS070379,Pelizaeus-Merzbacher disease null syndrome
+BMGC_DS18298,BMG_DS070407,Enteric Neuropathy
+BMGC_DS18299,BMG_DS070408,Congenital short bowel syndrome
+BMGC_DS18300,BMG_DS070410,interstitial lung disease
+BMGC_DS18301,BMG_DS070412,"Diarrhea 3, Secretory Sodium, Congenital"
+BMGC_DS18302,BMG_DS070413,"DIARRHEA 8, SECRETORY SODIUM, CONGENITAL"
+BMGC_DS18303,BMG_DS070415,Warburg micro syndrome
+BMGC_DS18304,BMG_DS070416,Congenital pontocerebellar hypoplasia type 1
+BMGC_DS18305,BMG_DS070417,"BLEEDING DISORDER, PLATELET-TYPE, 16"
+BMGC_DS18306,BMG_DS070418,"OTOFACIOCERVICAL SYNDROME 2, WITH T-CELL DEFICIENCY"
+BMGC_DS18307,BMG_DS070420,Clonal Cytopenia of Undetermined Significance
+BMGC_DS18308,BMG_DS070425,BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME
+BMGC_DS18309,BMG_DS070426,HYPERTRIGLYCERIDEMIA 1
+BMGC_DS18310,BMG_DS070427,COFFIN-SIRIS SYNDROME 12
+BMGC_DS18311,BMG_DS070428,"DYSOSTOSIS MULTIPLEX, AIN-NAZ TYPE"
+BMGC_DS18312,BMG_DS070429,"INFLAMMATORY BOWEL DISEASE (INFANTILE ULCERATIVE COLITIS) 31, AUTOSOMAL RECESSIVE"
+BMGC_DS18313,BMG_DS070430,Dentinogenesis Imperfecta 1
+BMGC_DS18314,BMG_DS070435,juvenile polyposis of infancy
+BMGC_DS18315,BMG_DS070442,autosomal recessive severe congenital neutropenia
+BMGC_DS18316,BMG_DS070444,Xq25 microduplication syndrome
+BMGC_DS18317,BMG_DS070445,lacrimal gland squamous cell carcinoma
+BMGC_DS18318,BMG_DS070503,Primary Vesicoureteral Reflux
+BMGC_DS18319,BMG_DS070504,VENTRICULAR ARRHYTHMIAS DUE TO CARDIAC RYANODINE RECEPTOR CALCIUM RELEASE DEFICIENCY SYNDROME
+BMGC_DS18320,BMG_DS070505,HYPOTAURINEMIC RETINAL DEGENERATION AND CARDIOMYOPATHY
+BMGC_DS18321,BMG_DS070506,VISCERAL MYOPATHY 1
+BMGC_DS18322,BMG_DS070507,ODONTOCHONDRODYSPLASIA 1
+BMGC_DS18323,BMG_DS070508,WHIM SYNDROME 1
+BMGC_DS18324,BMG_DS070509,MARTSOLF SYNDROME 1
+BMGC_DS18325,BMG_DS070510,MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 1
+BMGC_DS18326,BMG_DS070511,"MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED"
+BMGC_DS18327,BMG_DS070512,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 90
+BMGC_DS18328,BMG_DS070513,"SPERMATOGENIC FAILURE, X-LINKED, 3"
+BMGC_DS18329,BMG_DS070514,"AZOOSPERMIA, OBSTRUCTIVE, WITH NEPHROLITHIASIS"
+BMGC_DS18330,BMG_DS070516,"HYPERCHOLANEMIA, FAMILIAL 1"
+BMGC_DS18331,BMG_DS070517,OLMSTED SYNDROME 1
+BMGC_DS18332,BMG_DS070518,"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"
+BMGC_DS18334,BMG_DS070520,IMMUNODEFICIENCY 76
+BMGC_DS18335,BMG_DS070521,"NEURODEGENERATION, CHILDHOOD-ONSET, WITH HYPOTONIA, RESPIRATORY INSUFFICIENCY, AND BRAIN IMAGING ABNORMALITIES"
+BMGC_DS18336,BMG_DS070522,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 5
+BMGC_DS18337,BMG_DS070523,SPERMATOGENIC FAILURE 51
+BMGC_DS18338,BMG_DS070524,MYOFIBRILLAR MYOPATHY 11
+BMGC_DS18339,BMG_DS070525,"MICROCEPHALY 26, PRIMARY, AUTOSOMAL DOMINANT"
+BMGC_DS18340,BMG_DS070526,"MICROCEPHALY 27, PRIMARY, AUTOSOMAL DOMINANT"
+BMGC_DS18341,BMG_DS070527,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 4
+BMGC_DS18342,BMG_DS070528,"SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES 2"
+BMGC_DS18343,BMG_DS070529,JOUBERT SYNDROME 37
+BMGC_DS18344,BMG_DS070530,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 64"
+BMGC_DS18345,BMG_DS070531,LI-CAMPEAU SYNDROME
+BMGC_DS18346,BMG_DS070532,"EPILEPSY, PROGRESSIVE MYOCLONIC, 12"
+BMGC_DS18347,BMG_DS070533,NEUROFACIOSKELETAL SYNDROME WITH OR WITHOUT RENAL AGENESIS
+BMGC_DS18348,BMG_DS070534,"DEAFNESS, CONGENITAL, AND ADULT-ONSET PROGRESSIVE LEUKOENCEPHALOPATHY"
+BMGC_DS18349,BMG_DS070536,"NEPHROTIC SYNDROME, TYPE 23"
+BMGC_DS18350,BMG_DS070537,SPERMATOGENIC FAILURE 52
+BMGC_DS18351,BMG_DS070538,PREMATURE OVARIAN FAILURE 18
+BMGC_DS18352,BMG_DS070539,OLMSTED SYNDROME 2
+BMGC_DS18353,BMG_DS070540,ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 7
+BMGC_DS18354,BMG_DS070541,OCULOMOTOR-ABDUCENS SYNKINESIS
+BMGC_DS18355,BMG_DS070542,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL RECESSIVE 7"
+BMGC_DS18356,BMG_DS070543,"ENDOVE SYNDROME, LIMB-ONLY TYPE"
+BMGC_DS18357,BMG_DS070544,"ENDOVE SYNDROME, LIMB-BRAIN TYPE"
+BMGC_DS18358,BMG_DS070545,"Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome"
+BMGC_DS18359,BMG_DS070546,SULFIDE:QUINONE OXIDOREDUCTASE DEFICIENCY
+BMGC_DS18360,BMG_DS070547,IMMUNODEFICIENCY 77
+BMGC_DS18361,BMG_DS070548,"MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 4"
+BMGC_DS18362,BMG_DS070549,"BLISTERING, ACANTHOLYTIC, OF ORAL AND LARYNGEAL MUCOSA"
+BMGC_DS18363,BMG_DS070550,"VERTEBRAL, CARDIAC, TRACHEOESOPHAGEAL, RENAL, AND LIMB DEFECTS"
+BMGC_DS18364,BMG_DS070551,DEVELOPMENTAL DELAY WITH DYSMORPHIC FACIES AND DENTAL ANOMALIES
+BMGC_DS18365,BMG_DS070552,DEN HOED-DE BOER-VOISIN SYNDROME
+BMGC_DS18366,BMG_DS070553,BILE ACID CONJUGATION DEFECT 1
+BMGC_DS18367,BMG_DS070554,"SHORT STATURE, OLIGODONTIA, DYSMORPHIC FACIES, AND MOTOR DELAY"
+BMGC_DS18368,BMG_DS070555,IMMUNODEFICIENCY 79
+BMGC_DS18369,BMG_DS070556,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES
+BMGC_DS18370,BMG_DS070557,GLOBAL DEVELOPMENTAL DELAY WITH SPEECH AND BEHAVIORAL ABNORMALITIES
+BMGC_DS18371,BMG_DS070558,NEURODEVELOPMENTAL DISORDER WITH CEREBRAL ATROPHY AND VARIABLE FACIAL DYSMORPHISM
+BMGC_DS18372,BMG_DS070559,PREMATURE OVARIAN FAILURE 19
+BMGC_DS18373,BMG_DS070560,BARALLE-MACKEN SYNDROME
+BMGC_DS18374,BMG_DS070561,"HYPERCHOLANEMIA, FAMILIAL, 2"
+BMGC_DS18375,BMG_DS070562,SPERMATOGENIC FAILURE 53
+BMGC_DS18376,BMG_DS070563,NEURODEGENERATION WITH ATAXIA AND LATE-ONSET OPTIC ATROPHY
+BMGC_DS18377,BMG_DS070564,"SPONDYLOEPIPHYSEAL DYSPLASIA, SENSORINEURAL HEARING LOSS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND LEBER CONGENITAL AMAUROSIS"
+BMGC_DS18378,BMG_DS070565,"NEPHROTIC SYNDROME, TYPE 24"
+BMGC_DS18379,BMG_DS070566,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND VARIABLE SEIZURES
+BMGC_DS18380,BMG_DS070567,GLANZMANN THROMBASTHENIA 2
+BMGC_DS18381,BMG_DS070568,ALZAHRANI-KUWAHARA SYNDROME
+BMGC_DS18382,BMG_DS070569,ODONTOCHONDRODYSPLASIA 2 WITH HEARING LOSS AND DIABETES
+BMGC_DS18383,BMG_DS070570,"BLEEDING DISORDER, PLATELET-TYPE, 24"
+BMGC_DS18384,BMG_DS070571,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 37"
+BMGC_DS18385,BMG_DS070572,CIMDAG syndrome
+BMGC_DS18386,BMG_DS070573,"DEAFNESS, AUTOSOMAL DOMINANT 80"
+BMGC_DS18387,BMG_DS070574,"MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME 2"
+BMGC_DS18388,BMG_DS070575,PARKINSONISM WITH POLYNEUROPATHY
+BMGC_DS18389,BMG_DS070576,"IMMUNODEFICIENCY 14B, AUTOSOMAL RECESSIVE"
+BMGC_DS18390,BMG_DS070577,"NEURODEVELOPMENTAL DISORDER WITH SPASTICITY, CATARACTS, AND CEREBELLAR HYPOPLASIA"
+BMGC_DS18391,BMG_DS070578,DYSTONIA 30
+BMGC_DS18392,BMG_DS070579,KINSSHIP SYNDROME
+BMGC_DS18393,BMG_DS070580,"PONTOCEREBELLAR HYPOPLASIA, TYPE 14"
+BMGC_DS18394,BMG_DS070581,"PONTOCEREBELLAR HYPOPLASIA, TYPE 15"
+BMGC_DS18395,BMG_DS070582,"PONTOCEREBELLAR HYPOPLASIA, TYPE 1E"
+BMGC_DS18396,BMG_DS070583,"PONTOCEREBELLAR HYPOPLASIA, TYPE 1F"
+BMGC_DS18397,BMG_DS070584,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND CEREBELLAR HYPOPLASIA
+BMGC_DS18398,BMG_DS070585,"LEUKODYSTROPHY, HYPOMYELINATING, 21"
+BMGC_DS18399,BMG_DS070586,HIATT-NEU-COOPER NEURODEVELOPMENTAL SYNDROME
+BMGC_DS18400,BMG_DS070587,RADIO-TARTAGLIA SYNDROME
+BMGC_DS18401,BMG_DS070588,IMMUNODEFICIENCY 80 WITH OR WITHOUT CONGENITAL CARDIOMYOPATHY
+BMGC_DS18402,BMG_DS070589,BURATTI-HAREL SYNDROME
+BMGC_DS18403,BMG_DS070590,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 6B
+BMGC_DS18404,BMG_DS070591,OCULOGASTROINTESTINAL NEURODEVELOPMENTAL SYNDROME
+BMGC_DS18405,BMG_DS070592,LYMPHATIC MALFORMATION 9
+BMGC_DS18406,BMG_DS070593,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 65"
+BMGC_DS18407,BMG_DS070594,"GROWTH RESTRICTION, HYPOPLASTIC KIDNEYS, ALOPECIA, AND DISTINCTIVE FACIES"
+BMGC_DS18408,BMG_DS070595,MARBACH-RUSTAD PROGEROID SYNDROME
+BMGC_DS18409,BMG_DS070596,NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND GINGIVAL OVERGROWTH
+BMGC_DS18410,BMG_DS070597,HYPERTRIGLYCERIDEMIA 2
+BMGC_DS18411,BMG_DS070598,CPE-related Prader-Willi-like syndrome
+BMGC_DS18412,BMG_DS070599,"LEUKODYSTROPHY, HYPOMYELINATING, 22"
+BMGC_DS18413,BMG_DS070600,"FIBROMUSCULAR DYSPLASIA, MULTIFOCAL"
+BMGC_DS18414,BMG_DS070601,NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND MOTOR DYSFUNCTION
+BMGC_DS18415,BMG_DS070602,ARTHROGRYPOSIS MULTIPLEX CONGENITA 6
+BMGC_DS18416,BMG_DS070603,"CATARACTS, SPASTIC PARAPARESIS, AND SPEECH DELAY"
+BMGC_DS18417,BMG_DS070604,BARTSOCAS-PAPAS SYNDROME 2
+BMGC_DS18418,BMG_DS070605,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 96
+BMGC_DS18419,BMG_DS070606,VISCERAL MYOPATHY 2
+BMGC_DS18420,BMG_DS070607,MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 2
+BMGC_DS18421,BMG_DS070608,"ATAXIA, INTENTION TREMOR, AND HYPOTONIA SYNDROME, CHILDHOOD-ONSET"
+BMGC_DS18422,BMG_DS070609,"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY"
+BMGC_DS18423,BMG_DS070610,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 22"
+BMGC_DS18424,BMG_DS070611,"ONYCHODYSTROPHY, OSTEODYSTROPHY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES SYNDROME"
+BMGC_DS18425,BMG_DS070612,"ANGIOEDEMA, HEREDITARY, 4"
+BMGC_DS18426,BMG_DS070613,"ANGIOEDEMA, HEREDITARY, 5"
+BMGC_DS18427,BMG_DS070614,MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 3
+BMGC_DS18428,BMG_DS070615,"ANGIOEDEMA, HEREDITARY, 6"
+BMGC_DS18429,BMG_DS070616,MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 4
+BMGC_DS18430,BMG_DS070617,"ANGIOEDEMA, HEREDITARY, 7"
+BMGC_DS18431,BMG_DS070618,"ANGIOEDEMA, HEREDITARY, 8"
+BMGC_DS18432,BMG_DS070619,LYMPHATIC MALFORMATION 10
+BMGC_DS18433,BMG_DS070620,"CARDIOMYOPATHY, DILATED, 2D"
+BMGC_DS18434,BMG_DS070621,NEURODEVELOPMENTAL DISORDER WITH INFANTILE EPILEPTIC SPASMS
+BMGC_DS18435,BMG_DS070622,IMMUNODEFICIENCY 81
+BMGC_DS18436,BMG_DS070623,"AUTOINFLAMMATORY SYNDROME, FAMILIAL, WITH OR WITHOUT IMMUNODEFICIENCY"
+BMGC_DS18437,BMG_DS070624,FAUNDES-BANKA SYNDROME
+BMGC_DS18438,BMG_DS070625,OSTEOOTOHEPATOENTERIC SYNDROME
+BMGC_DS18439,BMG_DS070626,SPERMATOGENIC FAILURE 54
+BMGC_DS18440,BMG_DS070627,SPERMATOGENIC FAILURE 55
+BMGC_DS18441,BMG_DS070628,IMMUNODEFICIENCY 82 WITH SYSTEMIC INFLAMMATION
+BMGC_DS18442,BMG_DS070629,"LEBER-LIKE HEREDITARY OPTIC NEUROPATHY, AUTOSOMAL RECESSIVE 1"
+BMGC_DS18443,BMG_DS070630,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES"
+BMGC_DS18444,BMG_DS070631,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 52
+BMGC_DS18445,BMG_DS070632,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 29"
+BMGC_DS18446,BMG_DS070633,"encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 10"
+BMGC_DS18447,BMG_DS070634,LYMPHATIC MALFORMATION 11
+BMGC_DS18448,BMG_DS070635,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 28"
+BMGC_DS18449,BMG_DS070636,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 30"
+BMGC_DS18450,BMG_DS070637,HYPOKALEMIC TUBULOPATHY AND DEAFNESS
+BMGC_DS18451,BMG_DS070638,WHIM SYNDROME 2
+BMGC_DS18452,BMG_DS070639,"NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET 2"
+BMGC_DS18453,BMG_DS070640,MARTSOLF SYNDROME 2
+BMGC_DS18454,BMG_DS070641,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 31"
+BMGC_DS18455,BMG_DS070642,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 53
+BMGC_DS18456,BMG_DS070643,MITOCHONDRIAL DNA DEPLETION SYNDROME 16B (NEUROOPHTHALMIC TYPE)
+BMGC_DS18457,BMG_DS070644,WHITE-KERNOHAN SYNDROME
+BMGC_DS18458,BMG_DS070645,MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 5
+BMGC_DS18459,BMG_DS070646,"CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 6"
+BMGC_DS18460,BMG_DS070647,"CILIARY DYSKINESIA, PRIMARY, 46"
+BMGC_DS18461,BMG_DS070648,"HYPERTRIIODOTHYRONINEMIA, FAMILIAL DYSALBUMINEMIC"
+BMGC_DS18462,BMG_DS070678,Neuroinflammatory Diseases
+BMGC_DS18463,BMG_DS070680,Dominantly-Inherited Spinocerebellar Ataxias
+BMGC_DS18464,BMG_DS070692,Chronic Condition
+BMGC_DS18465,BMG_DS070790,Recurrent infection due to specific granule deficiency
+BMGC_DS18466,BMG_DS070883,bullous diffuse cutaneous mastocytosis
+BMGC_DS18467,BMG_DS071119,Progressive supranuclear palsy corticobasal syndrome
+BMGC_DS18468,BMG_DS071124,Atypical glycine encephalopathy
+BMGC_DS18469,BMG_DS071125,Neonatal glycine encephalopathy
+BMGC_DS18470,BMG_DS071126,familial adenomatous polyposis due to 5q22.2 microdeletion
+BMGC_DS18471,BMG_DS071130,Infantile glycine encephalopathy
+BMGC_DS18472,BMG_DS071133,Autosomal dominant distal hereditary motor neuropathy
+BMGC_DS18473,BMG_DS071134,X-linked thrombocytopenia with normal platelets
+BMGC_DS18474,BMG_DS071188,Autosomal recessive distal hereditary motor neuropathy
+BMGC_DS18475,BMG_DS071189,Progressive supranuclear palsy parkinsonism syndrome
+BMGC_DS18476,BMG_DS071202,Crigler-Najjar syndrome
+BMGC_DS18477,BMG_DS071204,"HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2"
+BMGC_DS18478,BMG_DS071209,Trichuriasis
+BMGC_DS18479,BMG_DS071210,"DYSKINESIA WITH OROFACIAL INVOLVEMENT, AUTOSOMAL DOMINANT"
+BMGC_DS18480,BMG_DS071211,AICARDI-GOUTIERES SYNDROME 8
+BMGC_DS18481,BMG_DS071212,Infection of skin and/or subcutaneous tissue
+BMGC_DS18482,BMG_DS071214,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND THIN CORPUS CALLOSUM
+BMGC_DS18483,BMG_DS071215,NEUROOCULAR SYNDROME 1
+BMGC_DS18484,BMG_DS071217,"CEROID LIPOFUSCINOSIS, NEURONAL, 6A"
+BMGC_DS18485,BMG_DS071220,"Muscular Dystrophy, Distal, Late-Onset, Autosomal Recessive"
+BMGC_DS18486,BMG_DS071221,Typical absence seizure
+BMGC_DS18487,BMG_DS071223,testicular seminoma
+BMGC_DS18488,BMG_DS071224,coxa vara
+BMGC_DS18489,BMG_DS071227,"OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE"
+BMGC_DS18490,BMG_DS071229,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 21"
+BMGC_DS18491,BMG_DS071232,Generalized seborrheic dermatitis of infants
+BMGC_DS18492,BMG_DS071233,continuous spikes and waves during sleep
+BMGC_DS18493,BMG_DS071234,"erythroleukemia, familial, susceptibility to"
+BMGC_DS18494,BMG_DS071235,Miyoshi myopathy
+BMGC_DS18495,BMG_DS071240,SMARCA4-deficient sarcoma of thorax
+BMGC_DS18496,BMG_DS071241,"multiple system atrophy, cerebellar type"
+BMGC_DS18497,BMG_DS071242,"multiple system atrophy, parkinsonian type"
+BMGC_DS18498,BMG_DS071257,RASopathy
+BMGC_DS18499,BMG_DS071258,Intermediate epidermolysis bullosa simplex with cardiomyopathy
+BMGC_DS18500,BMG_DS071260,uterine ligament adenocarcinoma
+BMGC_DS18501,BMG_DS071261,uterine ligament mucinous adenocarcinoma
+BMGC_DS18502,BMG_DS071262,uterine ligament endometrioid adenocarcinoma
+BMGC_DS18503,BMG_DS071263,uterine ligament clear cell adenocarcinoma
+BMGC_DS18504,BMG_DS071264,endometrial type cervical adenomyoma
+BMGC_DS18505,BMG_DS071275,"EPIDERMOLYSIS BULLOSA SIMPLEX 1B, GENERALIZED INTERMEDIATE"
+BMGC_DS18506,BMG_DS071276,RETINITIS PIGMENTOSA 91
+BMGC_DS18507,BMG_DS071277,INTERSTITIAL LUNG DISEASE 2
+BMGC_DS18508,BMG_DS071278,"CEROID LIPOFUSCINOSIS, NEURONAL, 6B (KUFS TYPE)"
+BMGC_DS18509,BMG_DS071279,anencephaly 1
+BMGC_DS18510,BMG_DS071280,"LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS 1"
+BMGC_DS18511,BMG_DS071281,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, WITH PIGMENTARY MOSAICISM AND COARSE FACIES"
+BMGC_DS18512,BMG_DS071282,"epilepsy, idiopathic generalized, susceptibility to, 17"
+BMGC_DS18513,BMG_DS071283,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 11"
+BMGC_DS18514,BMG_DS071284,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2GG"
+BMGC_DS18515,BMG_DS071285,"BILE ACID MALABSORPTION, PRIMARY, 1"
+BMGC_DS18516,BMG_DS071286,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw, AUTOSOMAL RECESSIVE"
+BMGC_DS18517,BMG_DS071287,BARDET-BIEDL SYNDROME 22
+BMGC_DS18518,BMG_DS071288,"MYOPATHY, MYOFIBRILLAR, 12, INFANTILE-ONSET, WITH CARDIOMYOPATHY"
+BMGC_DS18519,BMG_DS071289,FOCAL SEGMENTAL GLOMERULOSCLEROSIS AND NEURODEVELOPMENTAL SYNDROME
+BMGC_DS18520,BMG_DS071290,RITSCHER-SCHINZEL SYNDROME 4
+BMGC_DS18521,BMG_DS071291,IMMUNODEFICIENCY 84
+BMGC_DS18522,BMG_DS071292,"encephalitis, acute, infection (viral)-induced, susceptibility to, 11"
+BMGC_DS18523,BMG_DS071293,"DIARRHEA 12, WITH MICROVILLUS ATROPHY"
+BMGC_DS18524,BMG_DS071294,RETINAL DYSTROPHY AND MICROVILLUS INCLUSION DISEASE
+BMGC_DS18525,BMG_DS071295,"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIE"
+BMGC_DS18526,BMG_DS071296,anencephaly 2
+BMGC_DS18527,BMG_DS071297,LUO-SCHOCH-YAMAMOTO SYNDROME
+BMGC_DS18528,BMG_DS071298,"MYASTHENIC SYNDROME, CONGENITAL, 7B, PRESYNAPTIC, AUTOSOMAL RECESSIVE"
+BMGC_DS18529,BMG_DS071299,"PORTAL HYPERTENSION, NONCIRRHOTIC, 2"
+BMGC_DS18530,BMG_DS071300,SICK SINUS SYNDROME 4
+BMGC_DS18531,BMG_DS071301,"VISCERAL NEUROPATHY, FAMILIAL, 2, AUTOSOMAL RECESSIVE"
+BMGC_DS18532,BMG_DS071302,"CILIARY DYSKINESIA, PRIMARY, 47, AND LISSENCEPHALY"
+BMGC_DS18533,BMG_DS071303,"USMANI-RIAZUDDIN SYNDROME, AUTOSOMAL DOMINANT"
+BMGC_DS18534,BMG_DS071304,NEPHRONOPHTHISIS-LIKE NEPHROPATHY 2
+BMGC_DS18535,BMG_DS071305,NEURODEVELOPMENTAL DISORDER WITH MOTOR AND SPEECH DELAY AND BEHAVIORAL ABNORMALITIES
+BMGC_DS18536,BMG_DS071306,VISS SYNDROME
+BMGC_DS18537,BMG_DS071307,OCULOPHARYNGODISTAL MYOPATHY 3
+BMGC_DS18538,BMG_DS071308,"developmental delay, impaired speech, and behavioral abnormalities"
+BMGC_DS18539,BMG_DS071309,JOUBERT SYNDROME 38
+BMGC_DS18540,BMG_DS071310,"FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 3, DIGENIC"
+BMGC_DS18541,BMG_DS071311,"FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 4, DIGENIC"
+BMGC_DS18542,BMG_DS071312,SHORT-RIB THORACIC DYSPLASIA 21 WITHOUT POLYDACTYLY
+BMGC_DS18543,BMG_DS071313,"BILE ACID MALABSORPTION, PRIMARY, 2"
+BMGC_DS18544,BMG_DS071314,"CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 2, AND AUTONOMIC DYSFUNCTION"
+BMGC_DS18545,BMG_DS071315,"CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 3"
+BMGC_DS18546,BMG_DS071316,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 6"
+BMGC_DS18547,BMG_DS071317,AICARDI-GOUTIERES SYNDROME 9
+BMGC_DS18548,BMG_DS071318,DEGCAGS SYNDROME
+BMGC_DS18549,BMG_DS071319,"SHORT STATURE, DAUBER-ARGENTE TYPE"
+BMGC_DS18550,BMG_DS071320,"Parkinson disease 24, autosomal dominant, susceptibility to"
+BMGC_DS18551,BMG_DS071321,"CARDIOMYOPATHY, DILATED, 2E"
+BMGC_DS18552,BMG_DS071322,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 2v"
+BMGC_DS18553,BMG_DS071323,"DEAFNESS, AUTOSOMAL DOMINANT 81"
+BMGC_DS18554,BMG_DS071324,VENTRICULOMEGALY AND ARTHROGRYPOSIS
+BMGC_DS18555,BMG_DS071325,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND DYSMORPHIC FACIES
+BMGC_DS18556,BMG_DS071326,CHOPRA-AMIEL-GORDON SYNDROME
+BMGC_DS18557,BMG_DS071327,IMMUNODEFICIENCY 85 AND AUTOIMMUNITY
+BMGC_DS18558,BMG_DS071328,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND BRAIN ABNORMALITIES
+BMGC_DS18559,BMG_DS071329,SPERMATOGENIC FAILURE 56
+BMGC_DS18560,BMG_DS071330,NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ABNORMALITIES
+BMGC_DS18561,BMG_DS071331,"MUSCULAR DYSTROPHY, CONGENITAL HEARING LOSS, AND OVARIAN INSUFFICIENCY SYNDROME"
+BMGC_DS18562,BMG_DS071332,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2FF"
+BMGC_DS18563,BMG_DS071333,"epilepsy, idiopathic generalized, susceptibility to, 18"
+BMGC_DS18564,BMG_DS071334,NEURODEVELOPMENTAL-CRANIOFACIAL SYNDROME WITH VARIABLE RENAL AND CARDIAC ABNORMALITIES
+BMGC_DS18565,BMG_DS071335,"ANEMIA, SIDEROBLASTIC, 5"
+BMGC_DS18566,BMG_DS071336,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIw"
+BMGC_DS18567,BMG_DS071337,"PONTOCEREBELLAR HYPOPLASIA, TYPE 16"
+BMGC_DS18568,BMG_DS071338,SPERMATOGENIC FAILURE 57
+BMGC_DS18569,BMG_DS071339,CONE-ROD DYSTROPHY 22
+BMGC_DS18570,BMG_DS071340,"BILIARY, RENAL, NEUROLOGIC, AND SKELETAL SYNDROME"
+BMGC_DS18571,BMG_DS071341,cerebral cavernous malformation 4
+BMGC_DS18572,BMG_DS071342,BOUDIN-MORTIER SYNDROME
+BMGC_DS18573,BMG_DS071343,"USMANI-RIAZUDDIN SYNDROME, AUTOSOMAL RECESSIVE"
+BMGC_DS18574,BMG_DS071344,IMMUNODEFICIENCY 86
+BMGC_DS18575,BMG_DS071345,"DEAFNESS, AUTOSOMAL RECESSIVE 118, WITH COCHLEAR APLASIA"
+BMGC_DS18576,BMG_DS071346,"INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA, IMPAIRED SPEECH, AND DYSMORPHIC FACIES"
+BMGC_DS18577,BMG_DS071347,"SHORT STATURE, IMPAIRED INTELLECTUAL DEVELOPMENT, MICROCEPHALY, HYPOTONIA, AND OCULAR ANOMALIES"
+BMGC_DS18578,BMG_DS071348,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 97
+BMGC_DS18579,BMG_DS071349,JOUBERT SYNDROME 39
+BMGC_DS18580,BMG_DS071350,DYSTONIA 31
+BMGC_DS18581,BMG_DS071351,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 27"
+BMGC_DS18582,BMG_DS071352,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2HH"
+BMGC_DS18583,BMG_DS071353,DEVELOPMENTAL DELAY WITH OR WITHOUT INTELLECTUAL IMPAIRMENT OR BEHAVIORAL ABNORMALITIES
+BMGC_DS18584,BMG_DS071354,"CEREBELLAR ATAXIA, BRAIN ABNORMALITIES, AND CARDIAC CONDUCTION DEFECTS"
+BMGC_DS18585,BMG_DS071355,NEURODEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND ATAXIA AND WITH OR WITHOUT SEIZURES
+BMGC_DS18586,BMG_DS071356,JOUBERT SYNDROME 40
+BMGC_DS18587,BMG_DS071357,SPERMATOGENIC FAILURE 58
+BMGC_DS18588,BMG_DS071358,"EPIDERMOLYSIS BULLOSA SIMPLEX 2B, GENERALIZED INTERMEDIATE"
+BMGC_DS18589,BMG_DS071359,CATARACT 49
+BMGC_DS18590,BMG_DS071360,"EPIDERMOLYSIS BULLOSA SIMPLEX 2C, LOCALIZED"
+BMGC_DS18591,BMG_DS071361,"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES"
+BMGC_DS18592,BMG_DS071362,"RHIZOMELIC DYSPLASIA, AIN-NAZ TYPE"
+BMGC_DS18593,BMG_DS071363,"EPIDERMOLYSIS BULLOSA SIMPLEX 2D, GENERALIZED, INTERMEDIATE OR SEVERE, AUTOSOMAL RECESSIVE"
+BMGC_DS18594,BMG_DS071364,"FETAL AKINESIA, RESPIRATORY INSUFFICIENCY, MICROCEPHALY, POLYMICROGYRIA, AND DYSMORPHIC FACIES"
+BMGC_DS18595,BMG_DS071365,GALLOWAY-MOWAT SYNDROME 9
+BMGC_DS18596,BMG_DS071366,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 98
+BMGC_DS18597,BMG_DS071367,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 99
+BMGC_DS18598,BMG_DS071368,"HETEROTAXY, VISCERAL, 11, AUTOSOMAL, WITH MALE INFERTILITY"
+BMGC_DS18599,BMG_DS071369,GALLOWAY-MOWAT SYNDROME 10
+BMGC_DS18600,BMG_DS071370,INTERSTITIAL LUNG DISEASE 1
+BMGC_DS18601,BMG_DS071371,RETINITIS PIGMENTOSA 92
+BMGC_DS18602,BMG_DS071372,"DEAFNESS, AUTOSOMAL RECESSIVE 119"
+BMGC_DS18603,BMG_DS071373,NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS AND SPASTICITY
+BMGC_DS18604,BMG_DS071374,"SPASTIC PARAPLEGIA 84, AUTOSOMAL RECESSIVE"
+BMGC_DS18605,BMG_DS071375,IMMUNODEFICIENCY 88
+BMGC_DS18606,BMG_DS071376,IMMUNODEFICIENCY 89 AND AUTOIMMUNITY
+BMGC_DS18607,BMG_DS071377,ACROMESOMELIC DYSPLASIA 4
+BMGC_DS18608,BMG_DS071378,DYSTONIA 32
+BMGC_DS18609,BMG_DS071379,"SPONDYLOMETAPHYSEAL DYSPLASIA, PAGNAMENTA TYPE"
+BMGC_DS18610,BMG_DS071380,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND GROSS MOTOR AND SPEECH DELAY
+BMGC_DS18611,BMG_DS071381,HENGEL-MAROOFIAN-SCHOLS SYNDROME
+BMGC_DS18612,BMG_DS071382,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 11
+BMGC_DS18613,BMG_DS071383,SPERMATOGENIC FAILURE 59
+BMGC_DS18614,BMG_DS071384,SPERMATOGENIC FAILURE 60
+BMGC_DS18615,BMG_DS071385,"DYSKINESIA WITH OROFACIAL INVOLVEMENT, AUTOSOMAL RECESSIVE"
+BMGC_DS18616,BMG_DS071386,ZAKI SYNDROME
+BMGC_DS18617,BMG_DS071387,NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS AND DYSKINESIA
+BMGC_DS18618,BMG_DS071388,IMMUNODEFICIENCY 92
+BMGC_DS18619,BMG_DS071389,"NEURODEVELOPMENTAL DISORDER, NONPROGRESSIVE, WITH SPASTICITY AND TRANSIENT OPISTHOTONUS"
+BMGC_DS18620,BMG_DS071390,LOEYS-DIETZ SYNDROME 6
+BMGC_DS18621,BMG_DS071391,"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 8, WITH OR WITHOUT HETEROTAXY"
+BMGC_DS18622,BMG_DS071392,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 7, WITH OR WITHOUT HEARING LOSS"
+BMGC_DS18623,BMG_DS071393,"LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS 2"
+BMGC_DS18624,BMG_DS071394,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 8"
+BMGC_DS18625,BMG_DS071395,OVARIAN DYSGENESIS 9
+BMGC_DS18626,BMG_DS071396,SPERMATOGENIC FAILURE 61
+BMGC_DS18627,BMG_DS071397,SPERMATOGENIC FAILURE 62
+BMGC_DS18628,BMG_DS071398,MARBACH-SCHAAF NEURODEVELOPMENTAL SYNDROME
+BMGC_DS18629,BMG_DS071399,"DYSTONIA, EARLY-ONSET, AND/OR SPASTIC PARAPLEGIA"
+BMGC_DS18630,BMG_DS071400,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND NEONATAL CHOLESTASIS"
+BMGC_DS18631,BMG_DS071401,"SPASTIC PARAPLEGIA 85, AUTOSOMAL RECESSIVE"
+BMGC_DS18632,BMG_DS071402,DYSTONIA 33
+BMGC_DS18633,BMG_DS071403,SPERMATOGENIC FAILURE 63
+BMGC_DS18634,BMG_DS071404,BRUNET-WAGNER NEURODEVELOPMENTAL SYNDROME
+BMGC_DS18635,BMG_DS071405,"TRICHOTHIODYSTROPHY 8, NONPHOTOSENSITIVE"
+BMGC_DS18636,BMG_DS071406,"TRICHOTHIODYSTROPHY 9, NONPHOTOSENSITIVE"
+BMGC_DS18637,BMG_DS071407,"AGAMMAGLOBULINEMIA 9, AUTOSOMAL RECESSIVE"
+BMGC_DS18638,BMG_DS071408,DEVELOPMENTAL DELAY WITH VARIABLE NEUROLOGIC AND BRAIN ABNORMALITIES
+BMGC_DS18639,BMG_DS071409,RAUCH-STEINDL SYNDROME
+BMGC_DS18640,BMG_DS071410,SPERMATOGENIC FAILURE 64
+BMGC_DS18641,BMG_DS071411,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 12
+BMGC_DS18642,BMG_DS071412,"MUCOPOLYSACCHARIDOSIS, TYPE X"
+BMGC_DS18643,BMG_DS071413,FERGUSON-BONNI NEURODEVELOPMENTAL SYNDROME
+BMGC_DS18644,BMG_DS071414,YOON-BELLEN NEURODEVELOPMENTAL SYNDROME
+BMGC_DS18645,BMG_DS071415,SPERMATOGENIC FAILURE 65
+BMGC_DS18646,BMG_DS071416,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw, AUTOSOMAL DOMINANT"
+BMGC_DS18647,BMG_DS071417,"MICROCEPHALY 28, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS18648,BMG_DS071418,IMMUNODEFICIENCY 87 AND AUTOIMMUNITY
+BMGC_DS18649,BMG_DS071419,Sd(a) POLYAGGLUTINATION SYNDROME
+BMGC_DS18650,BMG_DS071420,"HETEROTAXY, VISCERAL, 10, AUTOSOMAL, WITH MALE INFERTILITY"
+BMGC_DS18651,BMG_DS071421,IMMUNODEFICIENCY 91 AND HYPERINFLAMMATION
+BMGC_DS18652,BMG_DS071422,"LEUKODYSTROPHY, HYPOMYELINATING, 23, WITH ATAXIA, DEAFNESS, LIVER DYSFUNCTION, AND DILATED CARDIOMYOPATHY"
+BMGC_DS18653,BMG_DS071423,"CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 1"
+BMGC_DS18654,BMG_DS071424,CHROMOSOME 16q12 DUPLICATION SYNDROME
+BMGC_DS18655,BMG_DS071444,"ANOSMIA, ISOLATED CONGENITAL, X-LINKED"
+BMGC_DS18656,BMG_DS071446,"CHROMOSOME 1p36 DELETION SYNDROME, PROXIMAL"
+BMGC_DS18657,BMG_DS071453,mmd1 myopathy
+BMGC_DS18658,BMG_DS071477,Angelman syndrome due to maternal monosomy 15q11q13
+BMGC_DS18659,BMG_DS071499,Mayer Rokitansky Küster Hauser syndrome type 1
+BMGC_DS18660,BMG_DS071509,Glycogen storage disease due to muscle beta-enolase deficiency
+BMGC_DS18661,BMG_DS071649,"X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome"
+BMGC_DS18662,BMG_DS071650,Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
+BMGC_DS18663,BMG_DS071652,"Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome"
+BMGC_DS18664,BMG_DS071661,LRP5-related primary osteoporosis
+BMGC_DS18665,BMG_DS071703,MME-related autosomal dominant Charcot Marie Tooth disease type 2
+BMGC_DS18666,BMG_DS071704,"Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome"
+BMGC_DS18667,BMG_DS071705,"Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome"
+BMGC_DS18668,BMG_DS071706,"Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome"
+BMGC_DS18669,BMG_DS071707,"Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome"
+BMGC_DS18670,BMG_DS071708,"Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome"
+BMGC_DS18671,BMG_DS071709,C11ORF73-related autosomal recessive hypomyelinating leukodystrophy
+BMGC_DS18672,BMG_DS071710,Childhood-onset benign chorea with striatal involvement
+BMGC_DS18673,BMG_DS071711,Infantile-onset generalized dyskinesia with orofacial involvement
+BMGC_DS18674,BMG_DS071712,"Diaphanous related formin 1 related sensorineural hearing loss, thrombocytopenia syndrome"
+BMGC_DS18675,BMG_DS071713,"Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome"
+BMGC_DS18676,BMG_DS071715,RERE-related neurodevelopmental syndrome
+BMGC_DS18677,BMG_DS071716,DDX41-related hematologic malignancy predisposition syndrome
+BMGC_DS18678,BMG_DS071717,"Early-onset epilepsy, intellectual disability, brain anomalies syndrome"
+BMGC_DS18679,BMG_DS071718,TBCK-related intellectual disability syndrome
+BMGC_DS18680,BMG_DS071719,"Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome"
+BMGC_DS18681,BMG_DS071720,"Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome"
+BMGC_DS18682,BMG_DS071721,Autosomal recessive spastic paraplegia type 76
+BMGC_DS18683,BMG_DS071722,SIX2-related frontonasal dysplasia
+BMGC_DS18684,BMG_DS071723,Autosomal dominant Charcot-Marie-Tooth disease type 2W
+BMGC_DS18685,BMG_DS071724,"Split-foot malformation, mesoaxial polydactyly syndrome"
+BMGC_DS18686,BMG_DS071726,female infertility due to oocyte meiotic arrest
+BMGC_DS18687,BMG_DS071730,"Microcephaly, congenital cataract, psoriasiform dermatitis syndrome"
+BMGC_DS18688,BMG_DS071731,Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation
+BMGC_DS18689,BMG_DS071732,Prenatal-onset spinal muscular atrophy with congenital bone fractures
+BMGC_DS18690,BMG_DS071734,"X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome"
+BMGC_DS18691,BMG_DS071735,Adenylosuccinate synthetase-like 1-related distal myopathy
+BMGC_DS18692,BMG_DS071736,"Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome"
+BMGC_DS18693,BMG_DS071737,"X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability"
+BMGC_DS18694,BMG_DS071738,"Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome"
+BMGC_DS18695,BMG_DS071741,"Lethal hydranencephaly, diaphragmatic hernia syndrome"
+BMGC_DS18696,BMG_DS071744,"Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome"
+BMGC_DS18697,BMG_DS071745,Combined oxidative phosphorylation defect type 30
+BMGC_DS18698,BMG_DS071746,Combined oxidative phosphorylation defect type 29
+BMGC_DS18699,BMG_DS071747,Combined oxidative phosphorylation defect type 27
+BMGC_DS18700,BMG_DS071748,"Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome"
+BMGC_DS18701,BMG_DS071749,Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RORgamma receptor mutation
+BMGC_DS18702,BMG_DS071750,"Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome"
+BMGC_DS18703,BMG_DS071751,Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
+BMGC_DS18704,BMG_DS071758,Combined oxidative phosphorylation defect type 26
+BMGC_DS18705,BMG_DS071759,Combined oxidative phosphorylation defect type 25
+BMGC_DS18706,BMG_DS071760,Combined oxidative phosphorylation defect type 23
+BMGC_DS18707,BMG_DS071762,"Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome"
+BMGC_DS18708,BMG_DS071763,IL21-related infantile inflammatory bowel disease
+BMGC_DS18709,BMG_DS071764,Congenital generalized hypercontractile muscle stiffness syndrome
+BMGC_DS18710,BMG_DS071770,Methicillin resistant Staphylococcus aureus skin infection
+BMGC_DS18711,BMG_DS071810,PMP2-related Charcot-Marie-Tooth disease type 1
+BMGC_DS18712,BMG_DS071812,Autosomal recessive spastic paraplegia type 78
+BMGC_DS18713,BMG_DS071816,"Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome"
+BMGC_DS18714,BMG_DS071818,"Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome"
+BMGC_DS18715,BMG_DS071819,Hyperphenylalaninemia due to DNAJC12 deficiency
+BMGC_DS18716,BMG_DS071820,"Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome"
+BMGC_DS18717,BMG_DS071822,Oral-facial-digital syndrome with short stature and brachymesophalangia
+BMGC_DS18718,BMG_DS071851,"Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract"
+BMGC_DS18719,BMG_DS071852,"Metopic ridging, ptosis, facial dysmorphism syndrome"
+BMGC_DS18720,BMG_DS071853,Combined immunodeficiency due to moesin deficiency
+BMGC_DS18721,BMG_DS071854,Combined immunodeficiency due to GINS1 deficiency
+BMGC_DS18722,BMG_DS071855,Combined immunodeficiency due to TFRC deficiency
+BMGC_DS18723,BMG_DS071856,Erythrokeratodermia cardiomyopathy syndrome
+BMGC_DS18724,BMG_DS071857,"Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome"
+BMGC_DS18725,BMG_DS071858,BVES-related limb girdle muscular dystrophy
+BMGC_DS18726,BMG_DS071859,Familial patent arterial duct
+BMGC_DS18727,BMG_DS071860,NEK9-related lethal skeletal dysplasia
+BMGC_DS18728,BMG_DS071861,DYRK1A-related intellectual disability syndrome
+BMGC_DS18729,BMG_DS071903,"Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome"
+BMGC_DS18730,BMG_DS071905,Combined immunodeficiency due to CARMIL2 deficiency
+BMGC_DS18731,BMG_DS071906,"Growth delay, intellectual disability, hepatopathy syndrome"
+BMGC_DS18732,BMG_DS071907,Combined immunodeficiency due to CD70 deficiency
+BMGC_DS18733,BMG_DS071908,"Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome"
+BMGC_DS18734,BMG_DS071909,"CEBPE-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome"
+BMGC_DS18735,BMG_DS071912,HTRA1-related autosomal dominant cerebral small vessel disease
+BMGC_DS18736,BMG_DS071916,"Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome"
+BMGC_DS18737,BMG_DS071917,Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction
+BMGC_DS18738,BMG_DS071934,Atypical pantothenate kinase associated neurodegeneration
+BMGC_DS18739,BMG_DS071992,complex neurodevelopmental disorder
+BMGC_DS18740,BMG_DS071994,Familial steroid-resistant nephrotic syndrome with adrenal insufficiency
+BMGC_DS18741,BMG_DS071995,"STAG1-related intellectual disability, facial dysmorphism, gastroesophageal reflux syndrome"
+BMGC_DS18742,BMG_DS071996,"Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome"
+BMGC_DS18743,BMG_DS071997,"Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome"
+BMGC_DS18744,BMG_DS072003,Mucopolysaccharidosis-like plus disease
+BMGC_DS18745,BMG_DS072004,"Micrognathia, recurrent infections, behavioral abnormalities, mild intellectual disability syndrome"
+BMGC_DS18746,BMG_DS072005,"Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome"
+BMGC_DS18747,BMG_DS072017,Isolated generalized anhidrosis with normal sweat glands
+BMGC_DS18748,BMG_DS072018,Autosomal recessive spastic paraplegia type 74
+BMGC_DS18749,BMG_DS072019,Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene
+BMGC_DS18750,BMG_DS072021,"Intellectual disability, epilepsy, extrapyramidal syndrome"
+BMGC_DS18751,BMG_DS072022,"Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome"
+BMGC_DS18752,BMG_DS072023,tubulinopathy-associated dysgyria
+BMGC_DS18753,BMG_DS072025,Autosomal dominant thrombocytopenia with platelet secretion defect
+BMGC_DS18754,BMG_DS072027,"Short stature, brachydactyly, obesity, global developmental delay syndrome"
+BMGC_DS18755,BMG_DS072028,"Spastic paraplegia, severe developmental delay, epilepsy syndrome"
+BMGC_DS18756,BMG_DS072029,"GNB5-related intellectual disability, cardiac arrhythmia syndrome"
+BMGC_DS18757,BMG_DS072030,VPS11-related autosomal recessive hypomyelinating leukodystrophy
+BMGC_DS18758,BMG_DS072031,"Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome"
+BMGC_DS18759,BMG_DS072032,Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
+BMGC_DS18760,BMG_DS072033,Autosomal dominant spastic paraplegia type 9A
+BMGC_DS18761,BMG_DS072034,Autosomal dominant spastic paraplegia type 9B
+BMGC_DS18762,BMG_DS072035,Autosomal recessive spastic paraplegia type 9B
+BMGC_DS18763,BMG_DS072036,Autosomal dominant spastic paraplegia type 73
+BMGC_DS18764,BMG_DS072037,Autosomal recessive spastic paraplegia type 77
+BMGC_DS18765,BMG_DS072053,Autosomal recessive Charcot-Marie-Tooth disease type 2X
+BMGC_DS18766,BMG_DS072054,Autosomal dominant Charcot-Marie-Tooth disease type 2Z
+BMGC_DS18767,BMG_DS072055,Autosomal dominant Charcot-Marie-Tooth disease type 2Y
+BMGC_DS18768,BMG_DS072056,Autosomal recessive intermediate Charcot-Marie-Tooth disease type D
+BMGC_DS18769,BMG_DS072057,Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation
+BMGC_DS18770,BMG_DS072058,Severe autosomal recessive macrothrombocytopenia
+BMGC_DS18771,BMG_DS072059,Autosomal dominant Charcot-Marie-Tooth disease type 2V
+BMGC_DS18772,BMG_DS072060,Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect
+BMGC_DS18773,BMG_DS072061,DNAJB2-related Charcot-Marie-Tooth disease type 2
+BMGC_DS18774,BMG_DS072085,Combined oxidative phosphorylation defect type 28
+BMGC_DS18775,BMG_DS072087,"Macrocephaly, intellectual disability, left ventricular non compaction syndrome"
+BMGC_DS18776,BMG_DS072088,"Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome"
+BMGC_DS18777,BMG_DS072160,Heterotropia
+BMGC_DS18778,BMG_DS072165,Ventricular tachyarrhythmia
+BMGC_DS18779,BMG_DS072166,atelosteogenesis
+BMGC_DS18780,BMG_DS072167,Dihydrolipoamide dehydrogenase deficiency (disorder)
+BMGC_DS18781,BMG_DS072169,"Epileptic Encephalopathy, Early Infantile, 3"
+BMGC_DS18782,BMG_DS072171,"ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia"
+BMGC_DS18783,BMG_DS072172,Hereditary sensory and autonomic neuropathy type II
+BMGC_DS18784,BMG_DS072173,Hyaline fibromatosis syndrome
+BMGC_DS18785,BMG_DS072174,Infantile systemic hyalinosis (disorder)
+BMGC_DS18786,BMG_DS072176,CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2
+BMGC_DS18787,BMG_DS072177,Adenomyosis
+BMGC_DS18788,BMG_DS072179,"Encephalomyelitis, Allergic"
+BMGC_DS18789,BMG_DS072183,Lysosomal acid lipase deficiency
+BMGC_DS18790,BMG_DS072185,Discoid lupus erythematosus
+BMGC_DS18791,BMG_DS072186,Systemic sclerosis with limited cutaneous involvement
+BMGC_DS18792,BMG_DS072188,Parkes Weber syndrome
+BMGC_DS18793,BMG_DS072190,"PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC"
+BMGC_DS18794,BMG_DS072191,preeclampsia/eclampsia 1
+BMGC_DS18795,BMG_DS072192,catecholaminergic polymorphic ventricular tachycardia
+BMGC_DS18796,BMG_DS072194,Timothy syndrome type 1
+BMGC_DS18797,BMG_DS072195,Combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria
+BMGC_DS18798,BMG_DS072196,"PAROXYSMAL NONKINESIGENIC DYSKINESIA, 3, WITH OR WITHOUT GENERALIZED EPILEPSY"
+BMGC_DS18799,BMG_DS072197,Congenital disorder of glycosylation type II
+BMGC_DS18800,BMG_DS072198,Netherton Syndrome
+BMGC_DS18801,BMG_DS072200,"NAIL DISORDER, NONSYNDROMIC CONGENITAL, 7"
+BMGC_DS18802,BMG_DS072202,HYPOGONADOTROPIC HYPOGONADISM 24 WITH OR WITHOUT ANOSMIA
+BMGC_DS18803,BMG_DS072203,Mesomelic dysplasia of upper limb
+BMGC_DS18804,BMG_DS072204,Patterson Stevenson Fontaine syndrome
+BMGC_DS18805,BMG_DS072205,frontorhiny
+BMGC_DS18806,BMG_DS072206,malignant Sertoli-Leydig cell tumor of ovary
+BMGC_DS18807,BMG_DS072208,synpolydactyly type 1
+BMGC_DS18808,BMG_DS072209,IMMUNODEFICIENCY 48
+BMGC_DS18809,BMG_DS072211,MAGEL2-related Prader-Willi-like syndrome
+BMGC_DS18810,BMG_DS072212,Corticobasal syndrome
+BMGC_DS18811,BMG_DS072213,"DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES"
+BMGC_DS18812,BMG_DS072215,benign familial infantile epilepsy
+BMGC_DS18813,BMG_DS072216,"developmental delay, impaired speech, and behavioral abnormalities, with or without seizures"
+BMGC_DS18814,BMG_DS072219,"CRANIOTUBULAR DYSPLASIA, IKEGAWA TYPE"
+BMGC_DS18815,BMG_DS072222,autosomal recessive cerebellar ataxia
+BMGC_DS18816,BMG_DS072223,"AUTOINFLAMMATORY SYNDROME, FAMILIAL, X-LINKED, BEHCET-LIKE 2"
+BMGC_DS18817,BMG_DS072225,Severe primary trimethylaminuria
+BMGC_DS18818,BMG_DS072226,severe Canavan disease
+BMGC_DS18819,BMG_DS072230,Contactin associated protein 2-related developmental and epileptic encephalopathy
+BMGC_DS18820,BMG_DS072231,Atypical Timothy syndrome
+BMGC_DS18821,BMG_DS072248,"diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype"
+BMGC_DS18822,BMG_DS072249,infant-type hemispheric glioma
+BMGC_DS18823,BMG_DS072250,high-grade astrocytoma with piloid features
+BMGC_DS18824,BMG_DS072257,schwannomatosis 1
+BMGC_DS18825,BMG_DS072258,schwannomatosis 2
+BMGC_DS18826,BMG_DS072263,Autoimmune Encephalitis
+BMGC_DS18827,BMG_DS072278,Autosomal dominant limb girdle muscular dystrophy
+BMGC_DS18828,BMG_DS072459,"ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IIIa"
+BMGC_DS18829,BMG_DS072460,"EPIDERMOLYSIS BULLOSA, JUNCTIONAL 5B, WITH PYLORIC ATRESIA"
+BMGC_DS18830,BMG_DS072461,CAREY-FINEMAN-ZITER SYNDROME 1
+BMGC_DS18831,BMG_DS072462,"PULMONARY HYPERTENSION, PRIMARY, 5"
+BMGC_DS18832,BMG_DS072463,RESTRICTIVE DERMOPATHY 1
+BMGC_DS18833,BMG_DS072464,"THROMBOPHILIA, X-LINKED, DUE TO FACTOR VIII DEFECT"
+BMGC_DS18834,BMG_DS072465,"MYOPATHY, DISTAL, 7, ADULT-ONSET, X-LINKED"
+BMGC_DS18835,BMG_DS072466,"intellectual developmental disorder, X-linked, syndromic, Pilorge type"
+BMGC_DS18836,BMG_DS072467,"SPERMATOGENIC FAILURE, X-LINKED, 4"
+BMGC_DS18837,BMG_DS072468,"IMMUNODEFICIENCY 98 WITH AUTOINFLAMMATION, X-LINKED"
+BMGC_DS18838,BMG_DS072469,SYSTEMIC LUPUS ERYTHEMATOSUS 17
+BMGC_DS18839,BMG_DS072470,"AUTOINFLAMMATORY DISEASE, SYSTEMIC, X-LINKED"
+BMGC_DS18840,BMG_DS072471,IMMUNODEFICIENCY 102
+BMGC_DS18841,BMG_DS072472,STUVE-WIEDEMANN SYNDROME 1
+BMGC_DS18842,BMG_DS072473,"RETINITIS PIGMENTOSA 94, VARIABLE AGE AT ONSET"
+BMGC_DS18843,BMG_DS072474,IMMUNODEFICIENCY 104
+BMGC_DS18844,BMG_DS072475,"thyroid hormone metabolism, abnormal 1"
+BMGC_DS18845,BMG_DS072476,"MACROTHROMBOCYTOPENIA, ISOLATED, 1, AUTOSOMAL DOMINANT"
+BMGC_DS18846,BMG_DS072477,"3-METHYLGLUTACONIC ACIDURIA, TYPE VIIB"
+BMGC_DS18847,BMG_DS072478,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, IMPAIRED LANGUAGE, AND DYSMORPHIC FEATURES"
+BMGC_DS18848,BMG_DS072479,"CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 2"
+BMGC_DS18849,BMG_DS072480,"intellectual developmental disorder, autosomal dominant 69"
+BMGC_DS18850,BMG_DS072481,KNOBLOCH SYNDROME 2
+BMGC_DS18851,BMG_DS072482,"heterotaxy, visceral, 12, autosomal"
+BMGC_DS18852,BMG_DS072483,IMMUNODEFICIENCY 93 AND HYPERTROPHIC CARDIOMYOPATHY
+BMGC_DS18853,BMG_DS072484,"AGAMMAGLOBULINEMIA 10, AUTOSOMAL DOMINANT"
+BMGC_DS18854,BMG_DS072485,GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME 2
+BMGC_DS18855,BMG_DS072486,"intellectual developmental disorder, autosomal recessive 73"
+BMGC_DS18856,BMG_DS072487,HYPOGONADOTROPIC HYPOGONADISM 26 WITH OR WITHOUT ANOSMIA
+BMGC_DS18857,BMG_DS072488,INTELLECTUAL DISABILITY AND MYOPATHY SYNDROME
+BMGC_DS18858,BMG_DS072489,BRYANT-LI-BHOJ NEURODEVELOPMENTAL SYNDROME 1
+BMGC_DS18859,BMG_DS072490,BRYANT-LI-BHOJ NEURODEVELOPMENTAL SYNDROME 2
+BMGC_DS18860,BMG_DS072491,"DYSTONIA 34, MYOCLONIC"
+BMGC_DS18861,BMG_DS072492,NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT VARIABLE MOVEMENT OR BEHAVIORAL ABNORMALITIES
+BMGC_DS18862,BMG_DS072493,INCLUSION BODY MYOPATHY AND BRAIN WHITE MATTER ABNORMALITIES
+BMGC_DS18863,BMG_DS072494,"SPASTIC PARAPLEGIA 86, AUTOSOMAL RECESSIVE"
+BMGC_DS18864,BMG_DS072495,TEEBI HYPERTELORISM SYNDROME 2
+BMGC_DS18865,BMG_DS072496,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 54
+BMGC_DS18866,BMG_DS072497,"PARKINSONISM-DYSTONIA 3, CHILDHOOD-ONSET"
+BMGC_DS18867,BMG_DS072498,"CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1I"
+BMGC_DS18868,BMG_DS072499,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 55
+BMGC_DS18869,BMG_DS072500,NOONAN SYNDROME 14
+BMGC_DS18870,BMG_DS072501,"CARDIOMYOPATHY, DILATED, 2F"
+BMGC_DS18871,BMG_DS072502,IMMUNODEFICIENCY 94 WITH AUTOINFLAMMATION AND DYSMORPHIC FACIES
+BMGC_DS18872,BMG_DS072503,STUVE-WIEDEMANN SYNDROME 2
+BMGC_DS18873,BMG_DS072504,"HYPER-IgE SYNDROME 4A, AUTOSOMAL DOMINANT, WITH RECURRENT INFECTIONS"
+BMGC_DS18874,BMG_DS072505,HYPOGONADOTROPIC HYPOGONADISM 27 WITHOUT ANOSMIA
+BMGC_DS18875,BMG_DS072506,TESSADORI-BICKNELL-VAN HAAFTEN NEURODEVELOPMENTAL SYNDROME 1
+BMGC_DS18876,BMG_DS072507,TESSADORI-BICKNELL-VAN HAAFTEN NEURODEVELOPMENTAL SYNDROME 2
+BMGC_DS18877,BMG_DS072508,"CEREBELLAR DYSFUNCTION, IMPAIRED INTELLECTUAL DEVELOPMENT, AND HYPOGONADOTROPIC HYPOGONADISM"
+BMGC_DS18878,BMG_DS072509,KURY-ISIDOR SYNDROME
+BMGC_DS18879,BMG_DS072510,"CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1H"
+BMGC_DS18880,BMG_DS072511,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 6"
+BMGC_DS18881,BMG_DS072512,"MACROCEPHALY, NEURODEVELOPMENTAL DELAY, LYMPHOID HYPERPLASIA, AND PERSISTENT FETAL HEMOGLOBIN"
+BMGC_DS18882,BMG_DS072513,IMMUNODEFICIENCY 95
+BMGC_DS18883,BMG_DS072514,IMMUNODEFICIENCY 96
+BMGC_DS18884,BMG_DS072515,CONGENITAL DISORDER OF DEGLYCOSYLATION 2
+BMGC_DS18885,BMG_DS072516,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 100
+BMGC_DS18886,BMG_DS072517,MITOCHONDRIAL DNA DEPLETION SYNDROME 20 (MNGIE TYPE)
+BMGC_DS18887,BMG_DS072518,"MYOPIA 28, AUTOSOMAL RECESSIVE"
+BMGC_DS18888,BMG_DS072519,"EPIDERMOLYSIS BULLOSA, JUNCTIONAL 2A, INTERMEDIATE"
+BMGC_DS18889,BMG_DS072520,"EPIDERMOLYSIS BULLOSA, JUNCTIONAL 2B, SEVERE"
+BMGC_DS18890,BMG_DS072521,"EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3A, INTERMEDIATE"
+BMGC_DS18891,BMG_DS072522,"EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3B, SEVERE"
+BMGC_DS18892,BMG_DS072523,"ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IIIb, AUTOSOMAL RECESSIVE"
+BMGC_DS18893,BMG_DS072524,OCULOPHARYNGODISTAL MYOPATHY 4
+BMGC_DS18894,BMG_DS072525,RESTRICTIVE DERMOPATHY 2
+BMGC_DS18895,BMG_DS072526,"OSTEOGENESIS IMPERFECTA, TYPE XXII"
+BMGC_DS18896,BMG_DS072527,NEURODEVELOPMENTAL DISORDER WITH CENTRAL HYPOTONIA AND DYSMORPHIC FACIES
+BMGC_DS18897,BMG_DS072528,SPERMATOGENIC FAILURE 66
+BMGC_DS18898,BMG_DS072529,IMMUNODEFICIENCY 97 WITH AUTOINFLAMMATION
+BMGC_DS18899,BMG_DS072530,SPERMATOGENIC FAILURE 67
+BMGC_DS18900,BMG_DS072531,"DEAFNESS, AUTOSOMAL DOMINANT 82"
+BMGC_DS18901,BMG_DS072532,SPERMATOGENIC FAILURE 68
+BMGC_DS18902,BMG_DS072533,SPINOCEREBELLAR ATAXIA 49
+BMGC_DS18903,BMG_DS072534,"DEAFNESS, AUTOSOMAL DOMINANT 83"
+BMGC_DS18904,BMG_DS072535,"DEAFNESS, AUTOSOMAL DOMINANT 84"
+BMGC_DS18905,BMG_DS072536,"NEUTROPENIA, SEVERE CONGENITAL, 9, AUTOSOMAL DOMINANT"
+BMGC_DS18906,BMG_DS072537,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 101
+BMGC_DS18907,BMG_DS072538,"EPIDERMOLYSIS BULLOSA, JUNCTIONAL 5A, INTERMEDIATE"
+BMGC_DS18908,BMG_DS072539,"EPIDERMOLYSIS BULLOSA, JUNCTIONAL 6, WITH PYLORIC ATRESIA"
+BMGC_DS18909,BMG_DS072540,"AGAMMAGLOBULINEMIA 8B, AUTOSOMAL RECESSIVE"
+BMGC_DS18910,BMG_DS072541,"AORTIC ANEURYSM, FAMILIAL THORACIC 12"
+BMGC_DS18911,BMG_DS072542,SPERMATOGENIC FAILURE 69
+BMGC_DS18912,BMG_DS072543,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 75, WITH NEUROPSYCHIATRIC FEATURES AND VARIANT LISSENCEPHALY"
+BMGC_DS18913,BMG_DS072544,SPERMATOGENIC FAILURE 70
+BMGC_DS18914,BMG_DS072545,SPERMATOGENIC FAILURE 71
+BMGC_DS18915,BMG_DS072546,"AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT 3"
+BMGC_DS18916,BMG_DS072547,NEURODEVELOPMENTAL DISORDER WITH NEUROMUSCULAR AND SKELETAL ABNORMALITIES
+BMGC_DS18917,BMG_DS072548,OVARIAN DYSGENESIS 10
+BMGC_DS18918,BMG_DS072549,"3-METHYLGLUTACONIC ACIDURIA, TYPE VIIA"
+BMGC_DS18919,BMG_DS072550,"MACROTHROMBOCYTOPENIA, ISOLATED, 2, AUTOSOMAL DOMINANT"
+BMGC_DS18920,BMG_DS072551,INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT PERIPHERAL NEUROPATHY
+BMGC_DS18921,BMG_DS072552,RETINITIS PIGMENTOSA 93
+BMGC_DS18922,BMG_DS072553,IMMUNODEFICIENCY 99 WITH HYPOGAMMAGLOBULINEMIA AND AUTOIMMUNE CYTOPENIAS
+BMGC_DS18923,BMG_DS072554,"NEURODEGENERATION, CHILDHOOD-ONSET, WITH PROGRESSIVE MICROCEPHALY"
+BMGC_DS18924,BMG_DS072555,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 9"
+BMGC_DS18925,BMG_DS072556,"LEUKODYSTROPHY, HYPOMYELINATING, 24"
+BMGC_DS18926,BMG_DS072557,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES"
+BMGC_DS18927,BMG_DS072558,"thyroid hormone metabolism, abnormal, 2"
+BMGC_DS18928,BMG_DS072559,AUTOINFLAMMATORY-PANCYTOPENIA SYNDROME
+BMGC_DS18929,BMG_DS072560,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 32"
+BMGC_DS18930,BMG_DS072561,"LEUKODYSTROPHY, CHILDHOOD-ONSET, REMITTING"
+BMGC_DS18931,BMG_DS072562,SPERMATOGENIC FAILURE 72
+BMGC_DS18932,BMG_DS072563,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 10"
+BMGC_DS18933,BMG_DS072564,"CORNEAL DYSTROPHY, PUNCTIFORM AND POLYCHROMATIC PRE-DESCEMET"
+BMGC_DS18934,BMG_DS072565,IMMUNODEFICIENCY 101 (VARICELLA ZOSTER VIRUS-SPECIFIC)
+BMGC_DS18935,BMG_DS072566,PARENTI-MIGNOT NEURODEVELOPMENTAL SYNDROME
+BMGC_DS18936,BMG_DS072567,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 11"
+BMGC_DS18937,BMG_DS072568,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, NYSTAGMUS, AND SEIZURES"
+BMGC_DS18938,BMG_DS072569,DENTICI-NOVELLI NEURODEVELOPMENTAL SYNDROME
+BMGC_DS18939,BMG_DS072570,SPERMATOGENIC FAILURE 73
+BMGC_DS18940,BMG_DS072571,MECKEL SYNDROME 14
+BMGC_DS18941,BMG_DS072572,NEURODEVELOPMENTAL DISORDER WITH POOR GROWTH AND SKELETAL ANOMALIES
+BMGC_DS18942,BMG_DS072573,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 102
+BMGC_DS18943,BMG_DS072574,"OSTEOPOROSIS, CHILDHOOD- OR JUVENILE-ONSET, WITH DEVELOPMENTAL DELAY"
+BMGC_DS18944,BMG_DS072575,RENAL HYPODYSPLASIA/APLASIA 4
+BMGC_DS18945,BMG_DS072576,HOLOPROSENCEPHALY 14
+BMGC_DS18946,BMG_DS072577,"CARDIOMYOPATHY, DILATED, 2G"
+BMGC_DS18947,BMG_DS072578,HEPATORENOCARDIAC DEGENERATIVE FIBROSIS
+BMGC_DS18948,BMG_DS072579,"PERIPHERAL MOTOR NEUROPATHY, CHILDHOOD-ONSET, BIOTIN-RESPONSIVE"
+BMGC_DS18949,BMG_DS072580,NEURODEVELOPMENTAL DISORDER WITH LANGUAGE DELAY AND SEIZURES
+BMGC_DS18950,BMG_DS072581,"PONTOCEREBELLAR HYPOPLASIA, TYPE 17"
+BMGC_DS18951,BMG_DS072582,"intellectual developmental disorder, autosomal dominant 66"
+BMGC_DS18952,BMG_DS072583,INTELLECTUAL DEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND EARLY-ONSET DOPA-RESPONSIVE DYSTONIA-PARKINSONISM
+BMGC_DS18953,BMG_DS072584,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 103
+BMGC_DS18954,BMG_DS072585,"DYSTONIA 35, CHILDHOOD-ONSET"
+BMGC_DS18955,BMG_DS072586,NEURODEVELOPMENTAL DISORDER WITH DYSTONIA AND SEIZURES
+BMGC_DS18956,BMG_DS072587,IMMUNODEFICIENCY 105
+BMGC_DS18957,BMG_DS072588,"intellectual developmental disorder, autosomal dominant 67"
+BMGC_DS18958,BMG_DS072589,"intellectual developmental disorder, autosomal recessive 76"
+BMGC_DS18959,BMG_DS072590,"intellectual developmental disorder, autosomal dominant 68"
+BMGC_DS18960,BMG_DS072591,"IMMUNODEFICIENCY 106, SUSCEPTIBILITY TO VIRAL INFECTIONS"
+BMGC_DS18961,BMG_DS072592,SPERMATOGENIC FAILURE 74
+BMGC_DS18962,BMG_DS072593,PREMATURE OVARIAN FAILURE 20
+BMGC_DS18963,BMG_DS072594,CAREY-FINEMAN-ZITER SYNDROME 2
+BMGC_DS18964,BMG_DS072595,"WAARDENBURG SYNDROME, TYPE 2F"
+BMGC_DS18965,BMG_DS072596,SPERMATOGENIC FAILURE 75
+BMGC_DS18966,BMG_DS072598,TESSADORI-BICKNELL-VAN HAAFTEN NEURODEVELOPMENTAL SYNDROME 4
+BMGC_DS18967,BMG_DS072599,DWORSCHAK-PUNETHA NEURODEVELOPMENTAL SYNDROME
+BMGC_DS18968,BMG_DS072600,attention deficit-hyperactivity disorder 8
+BMGC_DS18969,BMG_DS072601,ACCES SYNDROME
+BMGC_DS18970,BMG_DS072602,NEUROCARDIOFACIODIGITAL SYNDROME
+BMGC_DS18971,BMG_DS072603,"CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 1"
+BMGC_DS18972,BMG_DS072604,CHILTON-OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
+BMGC_DS18973,BMG_DS072605,CHROMOSOME 2q23.1 DUPLICATION SYNDROME
+BMGC_DS18974,BMG_DS072606,CHROMOSOME Xq25 TRIPLICATION SYNDROME
+BMGC_DS18975,BMG_DS072607,DIFFUSE GASTRIC AND LOBULAR BREAST CANCER SYNDROME WITH CLEFT LIP AND WITH OR WITHOUT CLEFT PALATE
+BMGC_DS18976,BMG_DS072608,"HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2, INTERMEDIATE"
+BMGC_DS18977,BMG_DS072619,"ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IIIb"
+BMGC_DS18978,BMG_DS072625,CUBITUS VALGUS WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND UNUSUAL FACIES
+BMGC_DS18979,BMG_DS072626,CHROMOSOME Xq13 DUPLICATION SYNDROME
+BMGC_DS18980,BMG_DS072629,isolated congenital growth hormone deficiency
+BMGC_DS18981,BMG_DS072630,Mild hereditary factor IX deficiency disease
+BMGC_DS18982,BMG_DS072631,Moderate hereditary factor IX deficiency disease
+BMGC_DS18983,BMG_DS072632,Severe hereditary factor IX deficiency disease
+BMGC_DS18984,BMG_DS072633,T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
+BMGC_DS18985,BMG_DS072634,T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta
+BMGC_DS18986,BMG_DS072635,T-B+ severe combined immunodeficiency due to CD45 deficiency
+BMGC_DS18987,BMG_DS072638,male infertility due to globozoospermia
+BMGC_DS18988,BMG_DS072642,Joubert syndrome and related disorders
+BMGC_DS18989,BMG_DS072643,"46,XX ovotesticular disorder of sex development"
+BMGC_DS18990,BMG_DS072644,autosomal recessive ataxia due to PEX10 deficiency
+BMGC_DS18991,BMG_DS072645,APC-related attenuated familial adenomatous polyposis
+BMGC_DS18992,BMG_DS072646,acute neonatal citrullinemia type I
+BMGC_DS18993,BMG_DS072651,paternal 14q32.2 microdeletion syndrome
+BMGC_DS18994,BMG_DS072652,maternal 14q32.2 microdeletion syndrome
+BMGC_DS18995,BMG_DS072683,Alagille syndrome due to 20p12 microdeletion
+BMGC_DS18996,BMG_DS072684,Mowat-Wilson syndrome due to a ZEB2 point mutation
+BMGC_DS18997,BMG_DS072685,Okihiro syndrome due to 20q13 microdeletion
+BMGC_DS18998,BMG_DS072686,Okihiro syndrome due to a point mutation
+BMGC_DS18999,BMG_DS072692,peeling skin syndrome 1
+BMGC_DS19000,BMG_DS072722,isolated focal cortical dysplasia type Ia
+BMGC_DS19001,BMG_DS072723,isolated focal cortical dysplasia type IIb
+BMGC_DS19002,BMG_DS072725,congenital communicating hydrocephalus
+BMGC_DS19003,BMG_DS072726,"Pelizaeus-Merzbacher disease, connatal form"
+BMGC_DS19004,BMG_DS072729,"mucopolysaccharidosis type 6, slowly progressing"
+BMGC_DS19005,BMG_DS072730,"mucopolysaccharidosis type 6, rapidly progressing"
+BMGC_DS19006,BMG_DS072731,syndromic microphthalmia
+BMGC_DS19007,BMG_DS072735,qualitative or quantitative defects of dystrophin
+BMGC_DS19008,BMG_DS072736,LAMA2-related muscular dystrophy
+BMGC_DS19009,BMG_DS072737,caveolinopathy
+BMGC_DS19010,BMG_DS072740,familial ovarian cancer
+BMGC_DS19011,BMG_DS072741,papillary carcinoma of the corpus uteri
+BMGC_DS19012,BMG_DS072744,isolated congenitally uncorrected transposition of the great arteries
+BMGC_DS19013,BMG_DS072746,classic pantothenate kinase-associated neurodegeneration
+BMGC_DS19014,BMG_DS072747,"Niemann-Pick disease type C, juvenile neurologic onset"
+BMGC_DS19015,BMG_DS072748,Bockenheimer syndrome
+BMGC_DS19016,BMG_DS072749,"mucopolysaccharidosis type 2, attenuated form"
+BMGC_DS19017,BMG_DS072750,Combined immunodeficiency due to DOCK8 deficiency
+BMGC_DS19018,BMG_DS072752,mitochondrial oxidative phosphorylation disorder
+BMGC_DS19019,BMG_DS072754,isolated anophthalmia-microphthalmia syndrome
+BMGC_DS19020,BMG_DS072755,Hermansky-Pudlak syndrome without pulmonary fibrosis
+BMGC_DS19021,BMG_DS072756,Hermansky-Pudlak syndrome with pulmonary fibrosis
+BMGC_DS19022,BMG_DS072761,apolipoprotein A-II amyloidosis
+BMGC_DS19023,BMG_DS072762,Autosomal dominant generalized dystrophic epidermolysis bullosa
+BMGC_DS19024,BMG_DS072764,isolated congenital hypogonadotropic hypogonadism
+BMGC_DS19025,BMG_DS072765,progressive supranuclear palsy-progressive non-fluent aphasia syndrome
+BMGC_DS19026,BMG_DS072766,progressive supranuclear palsy-pure akinesia with gait freezing syndrome
+BMGC_DS19027,BMG_DS072768,hemoglobin Lepore-beta-thalassemia syndrome
+BMGC_DS19028,BMG_DS072771,acute megakaryoblastic leukemia without down syndrome
+BMGC_DS19029,BMG_DS072772,classic congenital lipoid adrenal hyperplasia due to STAR deficency
+BMGC_DS19030,BMG_DS072774,ABetaL34V amyloidosis
+BMGC_DS19031,BMG_DS072775,classic multiminicore myopathy
+BMGC_DS19032,BMG_DS072776,Multiple paraganglioma associated with polycythemia
+BMGC_DS19033,BMG_DS072781,"classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form"
+BMGC_DS19034,BMG_DS072782,"classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form"
+BMGC_DS19035,BMG_DS072784,Primary hypereosinophilic syndrome
+BMGC_DS19036,BMG_DS072786,autosomal recessive spastic ataxia
+BMGC_DS19037,BMG_DS072788,muscular dystrophy-dystroglycanopathy
+BMGC_DS19038,BMG_DS072789,"Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies"
+BMGC_DS19039,BMG_DS072790,Alexander disease type II
+BMGC_DS19040,BMG_DS072791,Hemolytic uremic syndrome with DGKE deficiency
+BMGC_DS19041,BMG_DS072792,"autosomal recessive cutis laxa type 2, classic type"
+BMGC_DS19042,BMG_DS072793,minimal pigment oculocutaneous albinism type 1
+BMGC_DS19043,BMG_DS072794,neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion
+BMGC_DS19044,BMG_DS072795,"pyruvate carboxylase deficiency, benign type"
+BMGC_DS19045,BMG_DS072796,"pyruvate carboxylase deficiency, infantile form"
+BMGC_DS19046,BMG_DS072797,"pyruvate carboxylase deficiency, severe neonatal type"
+BMGC_DS19047,BMG_DS072806,familial clubfoot due to PITX1 point mutation
+BMGC_DS19048,BMG_DS072807,familial clubfoot due to 5q31 microdeletion
+BMGC_DS19049,BMG_DS072808,tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria
+BMGC_DS19050,BMG_DS072810,4H leukodystrophy
+BMGC_DS19051,BMG_DS072812,pseudoxanthomatous diffuse cutaneous mastocytosis
+BMGC_DS19052,BMG_DS072818,methylcobalamin deficiency type cblDv1
+BMGC_DS19053,BMG_DS072819,"glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form"
+BMGC_DS19054,BMG_DS072820,"glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form"
+BMGC_DS19055,BMG_DS072821,"alpha-mannosidosis, adult form"
+BMGC_DS19056,BMG_DS072825,zygodactyly type 3
+BMGC_DS19057,BMG_DS072828,Symptomatic form of hemochromatosis type 1
+BMGC_DS19058,BMG_DS072829,intellectual disability syndrome due to a DYRK1A point mutation
+BMGC_DS19059,BMG_DS072831,hereditary neuroendocrine tumor of small intestine
+BMGC_DS19060,BMG_DS072832,Congenital insensitivity to pain with severe intellectual disability
+BMGC_DS19061,BMG_DS072834,19p13.3 microduplication syndrome
+BMGC_DS19062,BMG_DS072841,AXIN2-related attenuated familial adenomatous polyposis
+BMGC_DS19063,BMG_DS072843,mild phosphoribosylpyrophosphate synthetase superactivity
+BMGC_DS19064,BMG_DS072844,severe phosphoribosylpyrophosphate synthetase superactivity
+BMGC_DS19065,BMG_DS072847,adult-onset myasthenia gravis
+BMGC_DS19066,BMG_DS072848,"HSD10 disease, infantile type"
+BMGC_DS19067,BMG_DS072849,"HSD10 disease, neonatal type"
+BMGC_DS19068,BMG_DS072850,"multiple acyl-CoA dehydrogenase deficiency, mild type"
+BMGC_DS19069,BMG_DS072851,"multiple acyl-CoA dehydrogenase deficiency, severe neonatal type"
+BMGC_DS19070,BMG_DS072857,SIM1-related Prader-Willi-like syndrome
+BMGC_DS19071,BMG_DS072860,"Intellectual disability, expressive aphasia, facial dysmorphism syndrome"
+BMGC_DS19072,BMG_DS072861,"Combined immunodeficiency, enteropathy spectrum"
+BMGC_DS19073,BMG_DS072862,Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa
+BMGC_DS19074,BMG_DS072863,Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
+BMGC_DS19075,BMG_DS072872,"Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome"
+BMGC_DS19076,BMG_DS072873,undetermined early-onset epileptic encephalopathy
+BMGC_DS19077,BMG_DS072876,Postural orthostatic tachycardia syndrome due to norepinephrine transporter deficiency
+BMGC_DS19078,BMG_DS072881,Primary immunodeficiency with multifaceted aberrant lymphoid immunity
+BMGC_DS19079,BMG_DS072882,tremor-ataxia-central hypomyelination syndrome
+BMGC_DS19080,BMG_DS072888,3-methylglutaconic aciduria type 8
+BMGC_DS19081,BMG_DS072889,9q33.3q34.11 microdeletion syndrome
+BMGC_DS19082,BMG_DS072890,16p13.2 microdeletion syndrome
+BMGC_DS19083,BMG_DS072893,MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome
+BMGC_DS19084,BMG_DS072896,congenital bile acid synthesis defect
+BMGC_DS19085,BMG_DS072899,MYO5B-related progressive familial intrahepatic cholestasis
+BMGC_DS19086,BMG_DS072901,demyelinating hereditary motor and sensory neuropathy
+BMGC_DS19087,BMG_DS072905,Syndromic congenital sodium diarrhea
+BMGC_DS19088,BMG_DS072909,Primary triglyceride deposit cardiomyovasculopathy
+BMGC_DS19089,BMG_DS072912,Resistance to thyroid hormone due to mutation in thyroid hormone receptor alpha
+BMGC_DS19090,BMG_DS072913,acute mast cell leukemia
+BMGC_DS19091,BMG_DS072914,Congenital autosomal recessive small-platelet thrombocytopenia
+BMGC_DS19092,BMG_DS072915,chronic mast cell leukemia
+BMGC_DS19093,BMG_DS072919,AKT2-related familial partial lipodystrophy
+BMGC_DS19094,BMG_DS072921,Congenital primary lymphedema of Gordon
+BMGC_DS19095,BMG_DS072922,EPHB4-related lymphatic-related hydrops fetalis
+BMGC_DS19096,BMG_DS072923,KRT1-related diffuse nonepidermolytic keratoderma
+BMGC_DS19097,BMG_DS072924,progressive dementia with neuroserpin inclusion bodies
+BMGC_DS19098,BMG_DS072925,neurometabolic disorder due to serine deficiency
+BMGC_DS19099,BMG_DS072927,Myopathic Ehlers-Danlos syndrome
+BMGC_DS19100,BMG_DS072929,PLG-related hereditary angioedema with normal C1inh
+BMGC_DS19101,BMG_DS072930,Ulcerative pyoderma gangrenosum
+BMGC_DS19102,BMG_DS072931,vegetative pyoderma gangrenosum
+BMGC_DS19103,BMG_DS072933,SYNGAP1-related developmental and epileptic encephalopathy
+BMGC_DS19104,BMG_DS072936,Atypical hemolytic uremic syndrome with complement gene abnormality
+BMGC_DS19105,BMG_DS072938,early-onset familial hypoaldosteronism
+BMGC_DS19106,BMG_DS072940,autosomal dominant intermediate Charcot-Marie-Tooth disease
+BMGC_DS19107,BMG_DS072942,"Congenital insensitivity to pain, anosmia, neuropathic arthropathy"
+BMGC_DS19108,BMG_DS072943,autosomal recessive non-syndromic intellectual disability
+BMGC_DS19109,BMG_DS072944,Non-syndromic genetic hearing loss
+BMGC_DS19110,BMG_DS072945,"Congenital vertebral, cardiac, renal anomalies syndrome"
+BMGC_DS19111,BMG_DS072946,17q24.2 microdeletion syndrome
+BMGC_DS19112,BMG_DS072948,X-linked nonsyndromic hearing loss
+BMGC_DS19113,BMG_DS072949,Duane retraction syndrome with congenital deafness
+BMGC_DS19114,BMG_DS072952,mild phenylketonuria
+BMGC_DS19115,BMG_DS072954,"HSD10 disease, atypical type"
+BMGC_DS19116,BMG_DS072955,mild hyperphenylalaninemia
+BMGC_DS19117,BMG_DS072957,KLHL7-related Bohring Opitz-like syndrome
+BMGC_DS19118,BMG_DS072958,KLHL7-related Crisponi/cold-induced sweating-like syndrome
+BMGC_DS19119,BMG_DS072965,silver-Russell syndrome due to maternal uniparental disomy of chromosome 7
+BMGC_DS19120,BMG_DS072966,maternal uniparental disomy of chromosome 14
+BMGC_DS19121,BMG_DS072968,paternal uniparental disomy of chromosome 14
+BMGC_DS19122,BMG_DS072977,euthyroid dysprealbuminemic hyperthyroxinemia
+BMGC_DS19123,BMG_DS072978,KAT6B-related multiple congenital anomalies syndrome
+BMGC_DS19124,BMG_DS072979,AFib amyloidosis
+BMGC_DS19125,BMG_DS072981,AApoAI amyloidosis
+BMGC_DS19126,BMG_DS072982,ALys amyloidosis
+BMGC_DS19127,BMG_DS072985,Hypomyelination of early myelinating structures
+BMGC_DS19128,BMG_DS072991,Combined immunodeficiency due to RELA haploinsufficiency
+BMGC_DS19129,BMG_DS072993,complete atrioventricular canal-ventricle hypoplasia syndrome
+BMGC_DS19130,BMG_DS072997,"atrial septal defect, ostium primum type"
+BMGC_DS19131,BMG_DS073004,"GNAO1-related developmental delay, seizures, movement disorder spectrum"
+BMGC_DS19132,BMG_DS073005,congenital-onset Steinert myotonic dystrophy
+BMGC_DS19133,BMG_DS073006,juvenile-onset Steinert myotonic dystrophy
+BMGC_DS19134,BMG_DS073007,childhood-onset Steinert myotonic dystrophy
+BMGC_DS19135,BMG_DS073008,late-onset Steinert myotonic dystrophy
+BMGC_DS19136,BMG_DS073009,adult-onset Steinert myotonic dystrophy
+BMGC_DS19137,BMG_DS073010,"Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome"
+BMGC_DS19138,BMG_DS073011,"Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies"
+BMGC_DS19139,BMG_DS073012,B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)
+BMGC_DS19140,BMG_DS073013,B-lymphoblastic leukemia/lymphoma with TCF3-PBX1
+BMGC_DS19141,BMG_DS073015,Autosomal recessive isolated optic atrophy
+BMGC_DS19142,BMG_DS073016,neu-laxova syndrome due to 3-phosphoserine phosphatase deficiency
+BMGC_DS19143,BMG_DS073019,Angelman syndrome due to paternal uniparental disomy of chromosome 15
+BMGC_DS19144,BMG_DS073020,Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
+BMGC_DS19145,BMG_DS073021,"Cathepsin A-related arteriopathy, strokes, leukoencephalopathy"
+BMGC_DS19146,BMG_DS073024,Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial JAK1 deficiency
+BMGC_DS19147,BMG_DS073025,blepharophimosis-ptosis-epicanthus inversus syndrome type 2
+BMGC_DS19148,BMG_DS073026,"Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia"
+BMGC_DS19149,BMG_DS073027,blepharophimosis-ptosis-epicanthus inversus syndrome type 1
+BMGC_DS19150,BMG_DS073036,lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene cluster
+BMGC_DS19151,BMG_DS073047,non-syndromic non-specific multisutural craniosynostosis
+BMGC_DS19152,BMG_DS073061,SBDS-related severe neonatal spondylometaphyseal dysplasia
+BMGC_DS19153,BMG_DS073062,immune deficiency due to impaired neutrophil phagocytosis and migration
+BMGC_DS19154,BMG_DS073063,SAMD9L-associated autoinflammatory syndrome
+BMGC_DS19155,BMG_DS073064,familial hyperinflammatory lymphoproliferative immunodeficiency
+BMGC_DS19156,BMG_DS073065,early-onset autoimmunity-autoinflammation-immunodeficiency syndrome
+BMGC_DS19157,BMG_DS073066,CADINS disease
+BMGC_DS19158,BMG_DS073068,Intermediate DEND syndrome
+BMGC_DS19159,BMG_DS073072,Severe congenital nemaline myopathy
+BMGC_DS19160,BMG_DS073073,Intermediate nemaline myopathy
+BMGC_DS19161,BMG_DS073074,Typical nemaline myopathy
+BMGC_DS19162,BMG_DS073080,autosomal dominant non-syndromic intellectual disability
+BMGC_DS19163,BMG_DS073082,symptomatic form of hemophilia A in female carriers
+BMGC_DS19164,BMG_DS073083,symptomatic form of hemophilia B in female carriers
+BMGC_DS19165,BMG_DS073084,Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
+BMGC_DS19166,BMG_DS073085,Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2
+BMGC_DS19167,BMG_DS073086,Prader-Willi syndrome due to translocation
+BMGC_DS19168,BMG_DS073087,Prader-Willi syndrome due to imprinting mutation
+BMGC_DS19169,BMG_DS073088,peripheral precocious puberty
+BMGC_DS19170,BMG_DS073093,familial isolated hypoparathyroidism due to impaired PTH secretion
+BMGC_DS19171,BMG_DS073094,syndromic intellectual disability
+BMGC_DS19172,BMG_DS073096,inherited renal tubular disease
+BMGC_DS19173,BMG_DS073097,inherited neurodegenerative disorder
+BMGC_DS19174,BMG_DS073111,late infantile CACH syndrome
+BMGC_DS19175,BMG_DS073112,juvenile or adult CACH syndrome
+BMGC_DS19176,BMG_DS073113,congenital or early infantile CACH syndrome
+BMGC_DS19177,BMG_DS073120,plaque-form urticaria pigmentosa
+BMGC_DS19178,BMG_DS073121,typical urticaria pigmentosa
+BMGC_DS19179,BMG_DS073122,nodular urticaria pigmentosa
+BMGC_DS19180,BMG_DS073125,De novo thrombotic microangiopathy following transplant of kidney
+BMGC_DS19181,BMG_DS073131,maternal 14q32.2 hypermethylation syndrome
+BMGC_DS19182,BMG_DS073132,paternal 14q32.2 hypomethylation syndrome
+BMGC_DS19183,BMG_DS073133,Kleefstra syndrome due to a point mutation
+BMGC_DS19184,BMG_DS073138,Baraitser Winter cerebrofrontofacial syndrome
+BMGC_DS19185,BMG_DS073143,isolated Dandy-Walker malformation without hydrocephalus
+BMGC_DS19186,BMG_DS073144,isolated Dandy-Walker malformation with hydrocephalus
+BMGC_DS19187,BMG_DS073147,Autosomal semi-dominant severe lipodystrophic laminopathy
+BMGC_DS19188,BMG_DS073149,Symptomatic form of Coffin-Lowry syndrome in female carrier
+BMGC_DS19189,BMG_DS073152,hereditary inclusion-body myopathy
+BMGC_DS19190,BMG_DS073156,qualitative or quantitative defects of delta-sarcoglycan
+BMGC_DS19191,BMG_DS073158,qualitative or quantitative defects of alpha-sarcoglycan
+BMGC_DS19192,BMG_DS073165,qualitative or quantitative defects of perlecan
+BMGC_DS19193,BMG_DS073166,qualitative or quantitative defects of beta-myosin heavy chain (MYH7)
+BMGC_DS19194,BMG_DS073168,qualitative or quantitative defects of plectin
+BMGC_DS19195,BMG_DS073183,"Niemann-Pick disease type C, severe perinatal form"
+BMGC_DS19196,BMG_DS073184,"Niemann-Pick disease type C, late infantile neurologic onset"
+BMGC_DS19197,BMG_DS073185,"Niemann-Pick disease type C, severe early infantile neurologic onset"
+BMGC_DS19198,BMG_DS073186,"Niemann-Pick disease type C, adult neurologic onset"
+BMGC_DS19199,BMG_DS073196,silver-Russell syndrome due to an imprinting defect of 11p15
+BMGC_DS19200,BMG_DS073197,silver-Russell syndrome due to 11p15 microduplication
+BMGC_DS19201,BMG_DS073198,Beckwith-Wiedemann syndrome due to CDKN1C mutation
+BMGC_DS19202,BMG_DS073201,Beckwith-Wiedemann syndrome due to imprinting defect of 11p15
+BMGC_DS19203,BMG_DS073205,Beckwith-Wiedemann syndrome due to NSD1 mutation
+BMGC_DS19204,BMG_DS073210,non-classic congenital lipoid adrenal hyperplasia due to STAR deficency
+BMGC_DS19205,BMG_DS073214,null pituitary adenoma
+BMGC_DS19206,BMG_DS073216,Koolen-de Vries syndrome due to a point mutation
+BMGC_DS19207,BMG_DS073217,TRPV4-related bone disorder
+BMGC_DS19208,BMG_DS073218,non-hereditary retinoblastoma
+BMGC_DS19209,BMG_DS073227,"glycerol kinase deficiency, adult form"
+BMGC_DS19210,BMG_DS073231,"glycerol kinase deficiency, juvenile form"
+BMGC_DS19211,BMG_DS073248,inborn aminoacylase deficiency
+BMGC_DS19212,BMG_DS073250,intermediate severe Salla disease
+BMGC_DS19213,BMG_DS073253,"congenital vertical talus, unilateral"
+BMGC_DS19214,BMG_DS073258,Fever-associated acute infantile liver failure syndrome
+BMGC_DS19215,BMG_DS073259,familial gastric type 1 neuroendocrine tumor
+BMGC_DS19216,BMG_DS073265,Symptomatic form of fragile X syndrome in female carrier
+BMGC_DS19217,BMG_DS073267,Isolated focal non-epidermolytic palmoplantar keratoderma
+BMGC_DS19218,BMG_DS073268,"Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome"
+BMGC_DS19219,BMG_DS073269,"X-linked intellectual disability, hypotonia, movement disorder syndrome"
+BMGC_DS19220,BMG_DS073270,"X-linked intellectual disability, short stature, overweight syndrome"
+BMGC_DS19221,BMG_DS073271,"Megalencephaly, severe kyphoscoliosis, overgrowth syndrome"
+BMGC_DS19222,BMG_DS073274,DeSanto-Shinawi syndrome due to WAC point mutation
+BMGC_DS19223,BMG_DS073278,Angelman syndrome due to a point mutation
+BMGC_DS19224,BMG_DS073280,"Short stature, advanced bone age, early-onset osteoarthritis syndrome"
+BMGC_DS19225,BMG_DS073281,"X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome"
+BMGC_DS19226,BMG_DS073282,"Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome"
+BMGC_DS19227,BMG_DS073283,"Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome"
+BMGC_DS19228,BMG_DS073284,"Microcephalic primordial dwarfism, insulin resistance syndrome"
+BMGC_DS19229,BMG_DS073285,"Familial atrial tachyarrhythmia, infra-Hisian cardiac conduction disease"
+BMGC_DS19230,BMG_DS073286,PDE4D haploinsufficiency syndrome
+BMGC_DS19231,BMG_DS073289,early-onset posterior subcapsular cataract
+BMGC_DS19232,BMG_DS073290,early-onset lamellar cataract
+BMGC_DS19233,BMG_DS073293,"Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome"
+BMGC_DS19234,BMG_DS073295,susceptibility to localized juvenile periodontitis
+BMGC_DS19235,BMG_DS073297,hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome
+BMGC_DS19236,BMG_DS073302,Short rib polydactyly syndrome type 5
+BMGC_DS19237,BMG_DS073303,EMILIN-1-related connective tissue disease
+BMGC_DS19238,BMG_DS073304,acquired schizencephaly
+BMGC_DS19239,BMG_DS073305,Isolated neonatal sclerosing cholangitis
+BMGC_DS19240,BMG_DS073307,syndromic constitutional thrombocytopenia
+BMGC_DS19241,BMG_DS073309,"Primary hypomagnesemia, refractory seizures, intellectual disability syndrome"
+BMGC_DS19242,BMG_DS073327,muscular channelopathy
+BMGC_DS19243,BMG_DS073328,multiple congenital anomalies/dysmorphic syndrome
+BMGC_DS19244,BMG_DS073331,Pustular pyoderma gangrenosum
+BMGC_DS19245,BMG_DS073333,"Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome"
+BMGC_DS19246,BMG_DS073334,"Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome"
+BMGC_DS19247,BMG_DS073337,inherited aplastic anemia
+BMGC_DS19248,BMG_DS073338,"Early-onset calcifying leukoencephalopathy, skeletal dysplasia"
+BMGC_DS19249,BMG_DS073339,"Pancreatic agenesis, holoprosencephaly syndrome"
+BMGC_DS19250,BMG_DS073340,"Spastic ataxia, dysarthria due to glutaminase deficiency"
+BMGC_DS19251,BMG_DS073347,non-syndromic syndactyly
+BMGC_DS19252,BMG_DS073348,isolated macular dystrophy
+BMGC_DS19253,BMG_DS073354,LAMA5-related multisystemic syndrome
+BMGC_DS19254,BMG_DS073355,"Microcephaly, facial dysmorphism, ocular anomalies, multiple congenital anomalies syndrome"
+BMGC_DS19255,BMG_DS073356,"Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome"
+BMGC_DS19256,BMG_DS073358,"Diaphragmatic hernia, short bowel, asplenia syndrome"
+BMGC_DS19257,BMG_DS073361,Encephalopathy due to mitochondrial and peroxisomal fission defect
+BMGC_DS19258,BMG_DS073366,"46,XY disorder of sex development due to isolated 17,20-lyase deficiency"
+BMGC_DS19259,BMG_DS073367,inherited isolated nail anomaly
+BMGC_DS19260,BMG_DS073379,infantile epilepsy syndrome
+BMGC_DS19261,BMG_DS073382,childhood-onset epilepsy syndrome
+BMGC_DS19262,BMG_DS073383,"CCNK-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome"
+BMGC_DS19263,BMG_DS073384,"NRXN1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance"
+BMGC_DS19264,BMG_DS073387,renal tubular dysgenesis of genetic origin
+BMGC_DS19265,BMG_DS073398,"IRF2BPL-related regressive neurodevelopmental disorder, dystonia, seizures syndrome"
+BMGC_DS19266,BMG_DS073400,"SETD2-related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome"
+BMGC_DS19267,BMG_DS073402,FOXG1 syndrome due to intragenic alteration
+BMGC_DS19268,BMG_DS073403,juvenile sialidosis type 2
+BMGC_DS19269,BMG_DS073404,congenital sialidosis type 2
+BMGC_DS19270,BMG_DS073405,hereditary angioedema with normal C1inh not related to F12 or PLG variant
+BMGC_DS19271,BMG_DS073406,FGFR3-related chondrodysplasia
+BMGC_DS19272,BMG_DS073408,"X-linked intellectual disability, Sutherland-Haan type"
+BMGC_DS19273,BMG_DS073409,"X-linked intellectual disability, Golabi-Ito-hall type"
+BMGC_DS19274,BMG_DS073410,hamel cerebro-palato-cardiac syndrome
+BMGC_DS19275,BMG_DS073411,"X-linked intellectual disability, Porteous type"
+BMGC_DS19276,BMG_DS073412,late-onset nephronophthisis
+BMGC_DS19277,BMG_DS073416,Menke Hennekam syndrome
+BMGC_DS19278,BMG_DS073417,"TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome"
+BMGC_DS19279,BMG_DS073419,"GRIN2B-related developmental delay, intellectual disability, autism spectrum disorder"
+BMGC_DS19280,BMG_DS073423,early-onset nuclear cataract
+BMGC_DS19281,BMG_DS073428,Noonan syndrome and Noonan-related syndrome
+BMGC_DS19282,BMG_DS073442,hereditary peripheral neuropathy
+BMGC_DS19283,BMG_DS073443,myopathic intestinal pseudoobstruction
+BMGC_DS19284,BMG_DS073448,familial hypofibrinogenemia
+BMGC_DS19285,BMG_DS073456,lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to a point mutation
+BMGC_DS19286,BMG_DS073459,EGF-related primary hypomagnesemia with intellectual disability
+BMGC_DS19287,BMG_DS073460,primary hypomagnesemia-generalized seizures-intellectual disability-obesity syndrome
+BMGC_DS19288,BMG_DS073461,F12-associated cold autoinflammatory syndrome
+BMGC_DS19289,BMG_DS073462,"Developmental delay, immunodeficiency, leukoencephalopathy, hypohomocysteinemia syndrome"
+BMGC_DS19290,BMG_DS073464,Angelman syndrome due to imprinting defect in 15q11-q13
+BMGC_DS19291,BMG_DS073465,inborn disorder of cobalamin metabolism and transport
+BMGC_DS19292,BMG_DS073467,CELSR1-related late-onset primary lymphedema
+BMGC_DS19293,BMG_DS073530,Autosomal recessive amyotrophic lateral sclerosis type 1
+BMGC_DS19294,BMG_DS073876,"X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome"
+BMGC_DS19295,BMG_DS073916,Chronic antibiotic-refractory pouchitis
+BMGC_DS19296,BMG_DS073917,Familial chilblain lupus erythematosus
+BMGC_DS19297,BMG_DS073918,Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy
+BMGC_DS19298,BMG_DS073963,Lethal brain and heart developmental defects syndrome
+BMGC_DS19299,BMG_DS074056,Chronic Kidney Diseases of Uncertain Etiology
+BMGC_DS19300,BMG_DS074061,Perinatal Cytomegalovirus Infection
+BMGC_DS19301,BMG_DS074062,Childhood Idiopathic Nephrotic Syndrome
+BMGC_DS19302,BMG_DS074063,Complement 3 Glomerulopathies
+BMGC_DS19303,BMG_DS074087,Varicose Bronchiectasis
+BMGC_DS19304,BMG_DS074088,Major Adverse Cardiac Events
+BMGC_DS19305,BMG_DS074091,Dental Enamel Erosion
+BMGC_DS19306,BMG_DS074094,"cardiomyopathy, dilated, 1b"
+BMGC_DS19307,BMG_DS074096,Acid Maltase Deficiency
+BMGC_DS19308,BMG_DS074097,Localized non-Herlitz junctional epidermolysis bullosa
+BMGC_DS19309,BMG_DS074098,Autosomal recessive axonal neuropathy with neuromyotonia
+BMGC_DS19310,BMG_DS074103,"Short stature, developmental delay, congenital heart defect syndrome"
+BMGC_DS19311,BMG_DS074107,"Segawa syndrome, autosomal recessive"
+BMGC_DS19312,BMG_DS074108,"MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 1"
+BMGC_DS19313,BMG_DS074110,"PARKINSONISM-DYSTONIA 1, INFANTILE-ONSET"
+BMGC_DS19314,BMG_DS074112,Carnosinase Deficiency
+BMGC_DS19315,BMG_DS074113,Exercise-induced malignant hyperthermia
+BMGC_DS19316,BMG_DS074116,"Platyspondylic Lethal Skeletal Dysplasia, Luton Type"
+BMGC_DS19317,BMG_DS074117,"iron overload, susceptibility to"
+BMGC_DS19318,BMG_DS074118,Hereditary von Willebrand disease
+BMGC_DS19319,BMG_DS074121,NSAID-Exacerbated Respiratory Disease
+BMGC_DS19320,BMG_DS074407,Generalized inflammatory peeling skin syndrome
+BMGC_DS19321,BMG_DS074640,CARDIAC VALVULAR DYSPLASIA 1
+BMGC_DS19322,BMG_DS074641,"PSEUDOHYPOALDOSTERONISM, TYPE IB1, AUTOSOMAL RECESSIVE"
+BMGC_DS19323,BMG_DS074642,"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"
+BMGC_DS19325,BMG_DS074644,HIJAZI-REIS SYNDROME
+BMGC_DS19326,BMG_DS074645,"intellectual developmental disorder, X-linked 110"
+BMGC_DS19327,BMG_DS074646,"MICROPHTHALMIA, SYNDROMIC 16"
+BMGC_DS19328,BMG_DS074647,"SPASTIC PARAPLEGIA 87, AUTOSOMAL RECESSIVE"
+BMGC_DS19329,BMG_DS074648,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 104
+BMGC_DS19330,BMG_DS074649,NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND BRAIN ATROPHY
+BMGC_DS19331,BMG_DS074650,"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT, ABSENT LANGUAGE, CEREBRAL HYPOMYELINATION, AND BRAIN ATROPHY"
+BMGC_DS19332,BMG_DS074651,TUMOR PREDISPOSITION SYNDROME 2
+BMGC_DS19333,BMG_DS074652,"MACULAR DYSTROPHY, RETINAL, 4"
+BMGC_DS19334,BMG_DS074653,BRADDOCK-CAREY SYNDROME 1
+BMGC_DS19335,BMG_DS074654,BRADDOCK-CAREY SYNDROME 2
+BMGC_DS19336,BMG_DS074655,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 105 WITH HYPOPITUITARISM
+BMGC_DS19337,BMG_DS074656,GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 25
+BMGC_DS19338,BMG_DS074657,"IMMUNODEFICIENCY 107, SUSCEPTIBILITY TO INVASIVE STAPHYLOCOCCUS AUREUS INFECTION"
+BMGC_DS19339,BMG_DS074658,"intellectual developmental disorder, autosomal recessive 77"
+BMGC_DS19340,BMG_DS074659,NEURODEVELOPMENTAL DISORDER WITH SPEECH DELAY AND VARIABLE OCULAR ANOMALIES
+BMGC_DS19341,BMG_DS074660,"LIVER DISEASE, SEVERE CONGENITAL"
+BMGC_DS19342,BMG_DS074661,"NEURODEVELOPMENTAL DISORDER WITH INTENTION TREMOR, PYRAMIDAL SIGNS, DYSPRAXIA, AND OCULAR ANOMALIES"
+BMGC_DS19343,BMG_DS074662,"NEURODEVELOPMENTAL DISORDER WITH SPASTICITY, SEIZURES, AND BRAIN ABNORMALITIES"
+BMGC_DS19344,BMG_DS074663,PRIMORDIAL DWARFISM-IMMUNODEFICIENCY-LIPODYSTROPHY SYNDROME
+BMGC_DS19345,BMG_DS074664,INTELLECTUAL DEVELOPMENTAL DISORDER WITH MUSCLE TONE ABNORMALITIES AND DISTAL SKELETAL DEFECTS
+BMGC_DS19346,BMG_DS074665,"KERATODERMA-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL RECESSIVE"
+BMGC_DS19347,BMG_DS074666,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL RECESSIVE 6"
+BMGC_DS19348,BMG_DS074667,"DEVELOPMENTAL DELAY, HYPOTONIA, AND IMPAIRED LANGUAGE"
+BMGC_DS19349,BMG_DS074668,LYMPHATIC MALFORMATION 12
+BMGC_DS19350,BMG_DS074669,"ADVANCE SLEEP PHASE SYNDROME, FAMILIAL, 4"
+BMGC_DS19351,BMG_DS074670,"ARTHROGRYPOSIS, DISTAL, TYPE 11"
+BMGC_DS19352,BMG_DS074671,INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND DYSMORPHIC FACIES
+BMGC_DS19353,BMG_DS074672,"STICKLER SYNDROME, TYPE VI"
+BMGC_DS19354,BMG_DS074673,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, MOVEMENT ABNORMALITIES, AND SEIZURES"
+BMGC_DS19355,BMG_DS074674,"NEURODEVELOPMENTAL DISORDER WITH SEIZURES, MICROCEPHALY, AND BRAIN ABNORMALITIES"
+BMGC_DS19356,BMG_DS074675,"DIAPHRAGMATIC HERNIA 4, WITH CARDIOVASCULAR DEFECTS"
+BMGC_DS19357,BMG_DS074676,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SHORT STATURE, AND SPEECH DELAY"
+BMGC_DS19358,BMG_DS074677,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 106
+BMGC_DS19359,BMG_DS074678,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, LANGUAGE DELAY, AND SKELETAL DEFECTS WITH OR WITHOUT SEIZURES"
+BMGC_DS19360,BMG_DS074679,"CILIARY DYSKINESIA, PRIMARY, 48, WITHOUT SITUS INVERSUS"
+BMGC_DS19361,BMG_DS074680,developmental and epileptic encephalopathy 107
+BMGC_DS19362,BMG_DS074681,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND ABSENT LANGUAGE"
+BMGC_DS19363,BMG_DS074682,"DYSKERATOSIS CONGENITA, DIGENIC"
+BMGC_DS19364,BMG_DS074683,BONE MARROW FAILURE AND DIABETES MELLITUS SYNDROME
+BMGC_DS19365,BMG_DS074684,INTESTINAL DYSMOTILITY SYNDROME
+BMGC_DS19366,BMG_DS074685,"MICROCEPHALY 29, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS19367,BMG_DS074686,"NEPHROTIC SYNDROME, TYPE 26"
+BMGC_DS19368,BMG_DS074687,POLYCYSTIC KIDNEY DISEASE 7
+BMGC_DS19369,BMG_DS074688,"DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FACIAL FEATURES, AND SPARSE HAIR 2"
+BMGC_DS19370,BMG_DS074689,"DEVELOPMENTAL DELAY, BEHAVIORAL ABNORMALITIES, AND NEUROPSYCHIATRIC DISORDERS"
+BMGC_DS19371,BMG_DS074690,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CEREBRAL ATROPHY, AND VISUAL IMPAIRMENT"
+BMGC_DS19372,BMG_DS074691,CARDIAC VALVULAR DYSPLASIA 2
+BMGC_DS19373,BMG_DS074692,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2II"
+BMGC_DS19374,BMG_DS074693,"NEURODEVELOPMENTAL DISORDER WITH SHORT STATURE, PROMINENT FOREHEAD, AND FEEDING DIFFICULTIES"
+BMGC_DS19375,BMG_DS074694,BIRK-AHARONI SYNDROME
+BMGC_DS19376,BMG_DS074695,DIAMOND-BLACKFAN ANEMIA 21
+BMGC_DS19377,BMG_DS074696,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"
+BMGC_DS19379,BMG_DS074698,BENT BONE DYSPLASIA SYNDROME 2
+BMGC_DS19380,BMG_DS074699,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 10"
+BMGC_DS19381,BMG_DS074700,NEURODEVELOPMENTAL DISORDER WITH CRANIOFACIAL DYSMORPHISM AND SKELETAL DEFECTS
+BMGC_DS19382,BMG_DS074701,SPERMATOGENIC FAILURE 76
+BMGC_DS19383,BMG_DS074702,HYPERMETABOLISM DUE TO UNCOUPLED MITOCHONDRIAL OXIDATIVE PHOSPHORYLATION 2
+BMGC_DS19384,BMG_DS074703,INTELLECTUAL DEVELOPMENTAL DISORDER WITH OCULAR ANOMALIES AND DISTINCTIVE FACIAL FEATURES
+BMGC_DS19385,BMG_DS074704,"NEURODEGENERATION, CHILDHOOD-ONSET, WITH MULTISYSTEM INVOLVEMENT DUE TO MITOCHONDRIAL DYSFUNCTION"
+BMGC_DS19386,BMG_DS074705,NEURODEVELOPMENTAL DISORDER WITH EYE MOVEMENT ABNORMALITIES AND ATAXIA
+BMGC_DS19387,BMG_DS074706,DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL DISABILITY AND DYSMORPHIC FACIES
+BMGC_DS19388,BMG_DS074707,CLEIDOCRANIAL DYSPLASIA 2
+BMGC_DS19389,BMG_DS074708,RETINITIS PIGMENTOSA 95
+BMGC_DS19390,BMG_DS074709,SPERMATOGENIC FAILURE 77
+BMGC_DS19391,BMG_DS074710,"AMELOGENESIS IMPERFECTA, TYPE IK"
+BMGC_DS19392,BMG_DS074711,"SPASTIC PARAPLEGIA 88, AUTOSOMAL DOMINANT"
+BMGC_DS19393,BMG_DS074712,OROFACIODIGITAL SYNDROME XIX
+BMGC_DS19394,BMG_DS074713,"CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1J"
+BMGC_DS19395,BMG_DS074714,"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
+BMGC_DS19397,BMG_DS074716,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 108
+BMGC_DS19398,BMG_DS074717,"PSEUDOHYPOALDOSTERONISM, TYPE IB2, AUTOSOMAL RECESSIVE"
+BMGC_DS19399,BMG_DS074718,"PSEUDOHYPOALDOSTERONISM, TYPE IB3, AUTOSOMAL RECESSIVE"
+BMGC_DS19400,BMG_DS074719,"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 8"
+BMGC_DS19401,BMG_DS074720,"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 39"
+BMGC_DS19402,BMG_DS074721,"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 11"
+BMGC_DS19403,BMG_DS074722,"MYOPATHY WITH MYALGIA, INCREASED SERUM CREATINE KINASE, AND WITH OR WITHOUT EPISODIC RHABDOMYOLYSIS"
+BMGC_DS19404,BMG_DS074723,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 56
+BMGC_DS19405,BMG_DS074724,"DEVELOPMENTAL DELAY, LANGUAGE IMPAIRMENT, AND OCULAR ABNORMALITIES"
+BMGC_DS19406,BMG_DS074725,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 109
+BMGC_DS19407,BMG_DS074726,"ICHTHYOSIS, ANNULAR EPIDERMOLYTIC, 2"
+BMGC_DS19408,BMG_DS074727,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 110
+BMGC_DS19409,BMG_DS074728,"HYPOMAGNESEMIA 7, RENAL, WITH OR WITHOUT DILATED CARDIOMYOPATHY"
+BMGC_DS19410,BMG_DS074729,MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 4
+BMGC_DS19411,BMG_DS074730,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 13
+BMGC_DS19412,BMG_DS074731,RABIN-PAPPAS SYNDROME
+BMGC_DS19413,BMG_DS074732,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 11"
+BMGC_DS19414,BMG_DS074733,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 70"
+BMGC_DS19415,BMG_DS074734,SPINOCEREBELLAR ATAXIA 50
+BMGC_DS19416,BMG_DS074735,CONGENITAL MYOPATHY 15
+BMGC_DS19417,BMG_DS074736,"MUSCULAR DYSTROPHY, CONGENITAL, WITH OR WITHOUT SEIZURES"
+BMGC_DS19418,BMG_DS074737,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 57
+BMGC_DS19419,BMG_DS074738,SPERMATOGENIC FAILURE 78
+BMGC_DS19420,BMG_DS074739,"TOOTH AGENESIS, SELECTIVE, 10"
+BMGC_DS19421,BMG_DS074740,"SPINOCEREBELLAR ATAXIA 27B, LATE-ONSET"
+BMGC_DS19422,BMG_DS074741,HYPOTRICHOSIS 15
+BMGC_DS19423,BMG_DS074742,"MICROCEPHALY 30, PRIMARY, AUTOSOMAL RECESSIVE"
+BMGC_DS19424,BMG_DS074743,ATELIS SYNDROME 1
+BMGC_DS19425,BMG_DS074744,ATELIS SYNDROME 2
+BMGC_DS19426,BMG_DS074745,"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
+BMGC_DS19428,BMG_DS074747,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, DYSMORPHIC FACIES, AND SKIN ABNORMALITIES"
+BMGC_DS19429,BMG_DS074748,LACRIMOAURICULODENTODIGITAL SYNDROME 2
+BMGC_DS19430,BMG_DS074749,LACRIMOAURICULODENTODIGITAL SYNDROME 3
+BMGC_DS19431,BMG_DS074750,"NEURODEVELOPMENTAL DISORDER WITH POOR GROWTH, LARGE EARS, AND DYSMORPHIC FACIES"
+BMGC_DS19432,BMG_DS074751,OBESITY AND HYPOPIGMENTATION
+BMGC_DS19433,BMG_DS074752,SPERMATOGENIC FAILURE 79
+BMGC_DS19434,BMG_DS074753,"CILIARY DYSKINESIA, PRIMARY, 49, WITHOUT SITUS INVERSUS"
+BMGC_DS19435,BMG_DS074754,"THYROID HORMONE METABOLISM, ABNORMAL, 3"
+BMGC_DS19436,BMG_DS074755,INFLAMMATORY POIKILODERMA WITH HAIR ABNORMALITIES AND ACRAL KERATOSES
+BMGC_DS19437,BMG_DS074756,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIy"
+BMGC_DS19438,BMG_DS074757,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIz"
+BMGC_DS19439,BMG_DS074758,"CARDIOMYOPATHY, DILATED, 2H"
+BMGC_DS19440,BMG_DS074759,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 33"
+BMGC_DS19441,BMG_DS074760,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND ISCHIOPUBIC HYPOPLASIA
+BMGC_DS19442,BMG_DS074761,"HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 8"
+BMGC_DS19443,BMG_DS074762,"SPASTIC PARAPLEGIA 79A, AUTOSOMAL DOMINANT, WITH ATAXIA"
+BMGC_DS19444,BMG_DS074763,SPERMATOGENIC FAILURE 80
+BMGC_DS19445,BMG_DS074764,"DEAFNESS, AUTOSOMAL DOMINANT 85"
+BMGC_DS19446,BMG_DS074765,RETINITIS PIGMENTOSA 96
+BMGC_DS19447,BMG_DS074766,SHORT QT SYNDROME 7
+BMGC_DS19448,BMG_DS074767,"JOINT CONTRACTURES, OSTEOCHONDROMAS, AND B-CELL LYMPHOMA"
+BMGC_DS19449,BMG_DS074768,"RESPIRATORY INFECTIONS, RECURRENT, AND FAILURE TO THRIVE WITH OR WITHOUT DIARRHEA"
+BMGC_DS19450,BMG_DS074769,"rhabdomyolysis, susceptibility to, 1"
+BMGC_DS19451,BMG_DS074770,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 29, WITH POLYGLUCOSAN BODIES"
+BMGC_DS19452,BMG_DS074771,"DEAFNESS, AUTOSOMAL RECESSIVE 120"
+BMGC_DS19453,BMG_DS074772,TESSADORI-BICKNELL-VAN HAAFTEN NEURODEVELOPMENTAL SYNDROME 3
+BMGC_DS19454,BMG_DS074773,"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 12"
+BMGC_DS19455,BMG_DS074774,"CLEIDOCRANIAL DYSPLASIA 1, FORME FRUSTE, WITH BRACHYDACTYLY"
+BMGC_DS19456,BMG_DS074775,"CLEIDOCRANIAL DYSPLASIA 1, FORME FRUSTE, DENTAL ANOMALIES ONLY"
+BMGC_DS19457,BMG_DS074776,MEDULLOBLASTOMA PREDISPOSITION SYNDROME
+BMGC_DS19458,BMG_DS074777,FAMILIAL APOLIPOPROTEIN GENE CLUSTER DELETION SYNDROME
+BMGC_DS19459,BMG_DS074780,LADD SYNDROME 1
+BMGC_DS19460,BMG_DS074819,Genetic torsion dystonia
+BMGC_DS19461,BMG_DS074821,autosomal dominant nonsyndromic hearing loss
+BMGC_DS19462,BMG_DS074823,Familial isolated retinal arterial tortuosity
+BMGC_DS19463,BMG_DS074826,"Primary degenerative dementia of the Alzheimer type, presenile onset"
+BMGC_DS19464,BMG_DS074829,Arthrogryposis multiplex congenita
+BMGC_DS19465,BMG_DS074831,RETINITIS PIGMENTOSA-DEAFNESS SYNDROME
+BMGC_DS19466,BMG_DS074832,Familial multinodular goiter syndrome
+BMGC_DS19467,BMG_DS074834,Eruption of skin (disorder)
+BMGC_DS19468,BMG_DS074836,"NEPHROLITHIASIS, CALCIUM OXALATE, 1"
+BMGC_DS19469,BMG_DS074837,Lecithin cholesterol acyltransferase deficiency
+BMGC_DS19470,BMG_DS074838,neurofibromatosis type 1 due to NF1 mutation or intragenic deletion
+BMGC_DS19471,BMG_DS074840,"RIBOFLAVIN TRANSPORTER DEFICIENCY, TYPE 1"
+BMGC_DS19472,BMG_DS074841,"Liver Failure, Fulminant"
+BMGC_DS19473,BMG_DS074845,Bannwarth syndrome
+BMGC_DS19474,BMG_DS074846,L1 syndrome
+BMGC_DS19475,BMG_DS074847,X-linked complicated spastic paraplegia type 1
+BMGC_DS19476,BMG_DS074850,CARPAL TUNNEL SYNDROME 1
+BMGC_DS19477,BMG_DS074856,Isolated cytochrome C oxidase deficiency
+BMGC_DS19478,BMG_DS074857,"USHER SYNDROME, TYPE IIIA"
+BMGC_DS19479,BMG_DS074860,MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1
+BMGC_DS19480,BMG_DS074861,FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1
+BMGC_DS19481,BMG_DS074862,Triphalangeal thumb and polysyndactyly syndrome
+BMGC_DS19482,BMG_DS074866,COMPLEMENT COMPONENT 4B DEFICIENCY
+BMGC_DS19483,BMG_DS074867,Developmental and epileptic encephalopathy
+BMGC_DS19484,BMG_DS074870,LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER 1
+BMGC_DS19485,BMG_DS074871,LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER 5
+BMGC_DS19486,BMG_DS074873,"Infantile multisystem neurologic, endocrine, pancreatic disease"
+BMGC_DS19487,BMG_DS074874,Congenital cataract microcornea with corneal opacity
+BMGC_DS19488,BMG_DS074875,HOUGE-JANSSENS SYNDROME 1
+BMGC_DS19489,BMG_DS074876,"Craniosynostosis, microretrognathia, severe intellectual disability syndrome"
+BMGC_DS19490,BMG_DS074877,autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
+BMGC_DS19491,BMG_DS074879,"Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome"
+BMGC_DS19492,BMG_DS074884,Classic Refsum Disease
+BMGC_DS19493,BMG_DS074885,Adult Refsum Disease
+BMGC_DS19494,BMG_DS074887,Hereditary Motor And Sensory Neuropathy IV
+BMGC_DS19495,BMG_DS074893,craniofacial microsomia 2
+BMGC_DS19496,BMG_DS074895,EPIDERMOLYTIC HYPERKERATOSIS 1
+BMGC_DS19497,BMG_DS074896,Phytanic Acid Oxidase Deficiency
+BMGC_DS19498,BMG_DS074899,Heredopathia Atactica Polyneuritiformis
+BMGC_DS19499,BMG_DS075112,intermediate collagen VI-related muscular dystrophy
+BMGC_DS19500,BMG_DS075113,"CDK13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome"
+BMGC_DS19501,BMG_DS075144,Hao-Fountain syndrome due to USP7 mutation
+BMGC_DS19502,BMG_DS075145,"Marfanoid habitus, facial dysmorphism, skeletal abnormality, heart defect syndrome"
+BMGC_DS19503,BMG_DS075151,Digenic hemochromatosis
+BMGC_DS19504,BMG_DS075154,Combined immunodeficiency due to FCHO1 deficiency
+BMGC_DS19505,BMG_DS075155,SLC40A1-related hemochromatosis
+BMGC_DS19506,BMG_DS075156,isolated primary pigmented nodular adrenocortical disease
+BMGC_DS19507,BMG_DS075157,craniosynostosis-facial dysmorphism-chiari-1 malformation-developmental and language delay syndrome
+BMGC_DS19508,BMG_DS075158,"MYT1L-related developmental delay, intellectual disability, obesity syndrome"
+BMGC_DS19509,BMG_DS075163,genetic central precocious puberty in male
+BMGC_DS19510,BMG_DS075166,genetic central precocious puberty in female
+BMGC_DS19511,BMG_DS075173,"SMARCA2-related blepharophimosis, intellectual disability syndrome"
+BMGC_DS19512,BMG_DS075177,B-lymphoblastic leukemia/lymphoma with t(17;19)
+BMGC_DS19513,BMG_DS075178,B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2)
+BMGC_DS19514,BMG_DS075179,"Infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome"
+BMGC_DS19515,BMG_DS075180,"Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome"
+BMGC_DS19516,BMG_DS075183,autosomal recessive ataxia due to PEX2 deficiency
+BMGC_DS19517,BMG_DS075184,autosomal recessive ataxia due to PEX16 deficiency
+BMGC_DS19518,BMG_DS075186,PUM1-related cerebellar ataxia
+BMGC_DS19519,BMG_DS075187,CHD8 overgrowth syndrome
+BMGC_DS19520,BMG_DS075188,mesomelic dysplasia-digital anomalies-intellectual disability syndrome
+BMGC_DS19521,BMG_DS075746,Autonomic Central Nervous System Diseases
+BMGC_DS19522,BMG_DS075747,Non-Familial Dysautonomia
+BMGC_DS19523,BMG_DS075749,Mandibulofacial Dysostosis (MFD1)
+BMGC_DS19524,BMG_DS075750,Kunjin virus Infection
+BMGC_DS19525,BMG_DS075753,Septic Cavernous Sinusitis
+BMGC_DS19526,BMG_DS075754,Acute Regional Pain Syndrome
+BMGC_DS19527,BMG_DS075755,Chronic Regional Pain Syndrome
+BMGC_DS19528,BMG_DS075756,Mitochondrial Defect
+BMGC_DS19529,BMG_DS075758,Chronic Secondary Pain
+BMGC_DS19530,BMG_DS075765,"SPERMATOGENIC FAILURE, X-LINKED, 5"
+BMGC_DS19531,BMG_DS075766,"SPERMATOGENIC FAILURE, X-LINKED, 6"
+BMGC_DS19532,BMG_DS075767,"SPERMATOGENIC FAILURE, X-LINKED, 7"
+BMGC_DS19533,BMG_DS075768,"intellectual developmental disorder, X-linked 111"
+BMGC_DS19534,BMG_DS075769,"CATARACTS, HEARING IMPAIRMENT, NEPHROTIC SYNDROME, AND ENTEROCOLITIS 1"
+BMGC_DS19535,BMG_DS075770,"AUTOINFLAMMATORY DISEASE, MULTISYSTEM, WITH IMMUNE DYSREGULATION, X-LINKED"
+BMGC_DS19536,BMG_DS075771,"HEMOLYTIC UREMIC SYNDROME, ATYPICAL, 8, WITH RHIZOMELIC SHORT STATURE"
+BMGC_DS19537,BMG_DS075772,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 112"
+BMGC_DS19538,BMG_DS075773,prolonged electroretinal response suppression 1
+BMGC_DS19539,BMG_DS075774,"CONGENITAL MYOPATHY 4B, AUTOSOMAL RECESSIVE"
+BMGC_DS19540,BMG_DS075775,CONE-ROD DYSTROPHY 23
+BMGC_DS19541,BMG_DS075776,"MACULAR DYSTROPHY, RETINAL, 5"
+BMGC_DS19542,BMG_DS075777,"CARDIOMYOPATHY, DILATED, 1PP"
+BMGC_DS19543,BMG_DS075778,ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 15
+BMGC_DS19544,BMG_DS075780,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, DYSMORPHIC FACIES, AND SKELETAL ANOMALIES, WITH OR WITHOUT SEIZURES"
+BMGC_DS19545,BMG_DS075781,"intellectual developmental disorder, autosomal recessive 78"
+BMGC_DS19546,BMG_DS075782,"DEVELOPMENTAL DELAY WITH HYPOTONIA, MYOPATHY, AND BRAIN ABNORMALITIES"
+BMGC_DS19547,BMG_DS075783,"hydrocephalus, congenital, 5, susceptibility to"
+BMGC_DS19548,BMG_DS075784,NEURODEVELOPMENTAL DISORDER WITH POOR GROWTH AND BEHAVIORAL ABNORMALITIES
+BMGC_DS19549,BMG_DS075785,"LEUKODYSTROPHY, HYPOMYELINATING, 25"
+BMGC_DS19550,BMG_DS075786,LYMPHATIC MALFORMATION 13
+BMGC_DS19551,BMG_DS075787,EPISODIC KINESIGENIC DYSKINESIA 3
+BMGC_DS19552,BMG_DS075788,CONGENITAL MYOPATHY 18
+BMGC_DS19553,BMG_DS075789,"CARDIOMYOPATHY, DILATED, 1OO"
+BMGC_DS19554,BMG_DS075790,"NEURODEVELOPMENTAL DISORDER WITH SEIZURES, SPASTICITY, AND COMPLETE OR PARTIAL AGENESIS OF THE CORPUS CALLOSUM"
+BMGC_DS19555,BMG_DS075791,CATARACT 50 WITH OR WITHOUT GLAUCOMA
+BMGC_DS19556,BMG_DS075792,"CONGENITAL MYOPATHY 2B, SEVERE INFANTILE, AUTOSOMAL RECESSIVE"
+BMGC_DS19557,BMG_DS075793,"LEUKODYSTROPHY, HYPOMYELINATING, 26, WITH CHONDRODYSPLASIA"
+BMGC_DS19558,BMG_DS075794,neurodevelopmental disorder with absent speech and movement and behavioral abnormalities
+BMGC_DS19559,BMG_DS075795,"MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 23"
+BMGC_DS19560,BMG_DS075796,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 14
+BMGC_DS19561,BMG_DS075797,SPERMATOGENIC FAILURE 81
+BMGC_DS19562,BMG_DS075798,"CONGENITAL MYOPATHY 2C, SEVERE INFANTILE, AUTOSOMAL DOMINANT"
+BMGC_DS19563,BMG_DS075799,"DEAFNESS, AUTOSOMAL DOMINANT 86"
+BMGC_DS19564,BMG_DS075800,"DEAFNESS, AUTOSOMAL DOMINANT 87"
+BMGC_DS19565,BMG_DS075801,IMMUNODEFICIENCY 109 WITH LYMPHOPROLIFERATION
+BMGC_DS19566,BMG_DS075802,"DEAFNESS, AUTOSOMAL DOMINANT 88"
+BMGC_DS19567,BMG_DS075803,"DEAFNESS, AUTOSOMAL DOMINANT 89"
+BMGC_DS19568,BMG_DS075804,"AMYOTROPHIC LATERAL SCLEROSIS 27, JUVENILE"
+BMGC_DS19569,BMG_DS075805,"MYOPATHY, SARCOPLASMIC BODY"
+BMGC_DS19570,BMG_DS075806,"NEURODEVELOPMENTAL DISORDER WITH LANGUAGE DELAY AND BEHAVIORAL ABNORMALITIES, WITH OR WITHOUT SEIZURES"
+BMGC_DS19571,BMG_DS075807,"congenital heart defects, multiple types, 9"
+BMGC_DS19572,BMG_DS075808,AUTOINFLAMMATION WITH PULMONARY AND CUTANEOUS VASCULITIS
+BMGC_DS19573,BMG_DS075809,MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY 2
+BMGC_DS19574,BMG_DS075810,"PITUITARY HORMONE DEFICIENCY, COMBINED OR ISOLATED, 8"
+BMGC_DS19575,BMG_DS075811,NEUROOCULORENAL SYNDROME
+BMGC_DS19576,BMG_DS075812,NEURODEGENERATION AND SEIZURES DUE TO COPPER TRANSPORT DEFECT
+BMGC_DS19577,BMG_DS075813,CONGENITAL MYOPATHY 20
+BMGC_DS19578,BMG_DS075814,PREMATURE OVARIAN FAILURE 21
+BMGC_DS19579,BMG_DS075815,LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER 2
+BMGC_DS19580,BMG_DS075816,LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER 3
+BMGC_DS19581,BMG_DS075817,LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER 4
+BMGC_DS19582,BMG_DS075818,"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 12"
+BMGC_DS19583,BMG_DS075819,"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND SPEECH DELAY, WITH OR WITHOUT BRAIN ABNORMALITIES"
+BMGC_DS19584,BMG_DS075820,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 17
+BMGC_DS19585,BMG_DS075821,"HEMATURIA, BENIGN FAMILIAL, 2"
+BMGC_DS19586,BMG_DS075822,C1q DEFICIENCY 2
+BMGC_DS19587,BMG_DS075823,C1q DEFICIENCY 3
+BMGC_DS19588,BMG_DS075824,CONGENITAL MYOPATHY 21 WITH EARLY RESPIRATORY FAILURE
+BMGC_DS19589,BMG_DS075825,"NEURODEGENERATION WITH DEVELOPMENTAL DELAY, EARLY RESPIRATORY FAILURE, MYOCLONIC SEIZURES, AND BRAIN ABNORMALITIES"
+BMGC_DS19590,BMG_DS075826,"intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities"
+BMGC_DS19591,BMG_DS075827,HATIPOGLU IMMUNODEFICIENCY SYNDROME
+BMGC_DS19592,BMG_DS075828,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 18
+BMGC_DS19593,BMG_DS075829,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 19
+BMGC_DS19594,BMG_DS075830,CONE-ROD DYSTROPHY 24
+BMGC_DS19595,BMG_DS075831,basal cell nevus syndrome 2
+BMGC_DS19596,BMG_DS075832,prolonged electroretinal response suppression 2
+BMGC_DS19597,BMG_DS075833,"CONGENITAL MYOPATHY 22A, CLASSIC"
+BMGC_DS19598,BMG_DS075834,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 31B
+BMGC_DS19599,BMG_DS075835,SPERMATOGENIC FAILURE 82
+BMGC_DS19600,BMG_DS075836,SPERMATOGENIC FAILURE 83
+BMGC_DS19601,BMG_DS075837,"CILIARY DYSKINESIA, PRIMARY, 50"
+BMGC_DS19602,BMG_DS075838,DIARRHEA 13
+BMGC_DS19603,BMG_DS075839,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4A"
+BMGC_DS19604,BMG_DS075840,"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 7"
+BMGC_DS19605,BMG_DS075841,combined low LDL and fibrinogen
+BMGC_DS19606,BMG_DS075842,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 7"
+BMGC_DS19607,BMG_DS075843,"OSTEOPETROSIS, AUTOSOMAL RECESSIVE 9"
+BMGC_DS19608,BMG_DS075844,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 8"
+BMGC_DS19609,BMG_DS075845,CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 3
+BMGC_DS19610,BMG_DS075846,"CONGENITAL MYOPATHY 22B, SEVERE FETAL"
+BMGC_DS19611,BMG_DS075847,RECON PROGEROID SYNDROME
+BMGC_DS19612,BMG_DS075848,"NEURODEVELOPMENTAL DISORDER WITH INTRACRANIAL HEMORRHAGE, SEIZURES, AND SPASTICITY"
+BMGC_DS19613,BMG_DS075849,HYPERSULFATURIA
+BMGC_DS19614,BMG_DS075850,"NEPHROLITHIASIS, CALCIUM OXALATE, 2, WITH OR WITHOUT NEPHROCALCINOSIS"
+BMGC_DS19615,BMG_DS075851,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 28"
+BMGC_DS19616,BMG_DS075852,"AUTOINFLAMMATORY DISEASE, SYSTEMIC, WITH VASCULITIS"
+BMGC_DS19617,BMG_DS075853,"SPASTIC PARAPLEGIA 89, AUTOSOMAL RECESSIVE"
+BMGC_DS19618,BMG_DS075854,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 20
+BMGC_DS19619,BMG_DS075855,"AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT 2"
+BMGC_DS19620,BMG_DS075856,"NEMALINE MYOPATHY 5B, AUTOSOMAL RECESSIVE, CHILDHOOD-ONSET"
+BMGC_DS19621,BMG_DS075857,"NEMALINE MYOPATHY 5C, AUTOSOMAL DOMINANT"
+BMGC_DS19622,BMG_DS075858,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 79"
+BMGC_DS19623,BMG_DS075859,GLYCINE ENCEPHALOPATHY 2
+BMGC_DS19624,BMG_DS075860,"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 9"
+BMGC_DS19625,BMG_DS075861,SPERMATOGENIC FAILURE 84
+BMGC_DS19626,BMG_DS075862,"SPASTIC PARAPLEGIA 90A, AUTOSOMAL DOMINANT"
+BMGC_DS19627,BMG_DS075863,"SPASTIC PARAPLEGIA 90B, AUTOSOMAL RECESSIVE"
+BMGC_DS19628,BMG_DS075864,RETINITIS PIGMENTOSA 97
+BMGC_DS19629,BMG_DS075865,MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 7
+BMGC_DS19630,BMG_DS075866,"CATARACTS, HEARING IMPAIRMENT, NEPHROTIC SYNDROME, AND ENTEROCOLITIS 2"
+BMGC_DS19631,BMG_DS075867,"DYSTONIA 37, EARLY-ONSET, WITH STRIATAL LESIONS"
+BMGC_DS19632,BMG_DS075868,"NEURODEVELOPMENTAL DISORDER WITH MOTOR AND LANGUAGE DELAY, OCULAR DEFECTS, AND BRAIN ABNORMALITIES"
+BMGC_DS19633,BMG_DS075869,"AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 3"
+BMGC_DS19634,BMG_DS075870,"CILIARY DYSKINESIA, PRIMARY, 51"
+BMGC_DS19635,BMG_DS075871,"intellectual developmental disorder, autosomal dominant 72"
+BMGC_DS19636,BMG_DS075872,"breast-ovarian cancer, familial, susceptibility to, 5"
+BMGC_DS19637,BMG_DS075873,NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND MOVEMENT ABNORMALITIES
+BMGC_DS19638,BMG_DS075874,MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 3
+BMGC_DS19639,BMG_DS075875,"MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 4, REMITTING"
+BMGC_DS19640,BMG_DS075876,IMMUNODEFICIENCY 112
+BMGC_DS19641,BMG_DS075877,"intellectual developmental disorder, autosomal dominant 73"
+BMGC_DS19642,BMG_DS075878,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 58
+BMGC_DS19643,BMG_DS075879,AMYOTROPHIC LATERAL SCLEROSIS 28
+BMGC_DS19644,BMG_DS075880,"DYSTONIA 22, JUVENILE-ONSET"
+BMGC_DS19645,BMG_DS075881,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIaa"
+BMGC_DS19646,BMG_DS075882,"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND SPEECH DELAY, WITH OR WITHOUT SEIZURES"
+BMGC_DS19647,BMG_DS075883,"DYSTONIA 22, ADULT-ONSET"
+BMGC_DS19648,BMG_DS075884,AURICULOCONDYLAR SYNDROME 4
+BMGC_DS19649,BMG_DS075885,AURICULOCONDYLAR SYNDROME 2B
+BMGC_DS19650,BMG_DS075886,BIRT-HOGG-DUBE SYNDROME 2
+BMGC_DS19651,BMG_DS075887,OCULOPHARYNGEAL MUSCULAR DYSTROPHY 2
+BMGC_DS19652,BMG_DS075888,"CARDIOMYOPATHY, DILATED, 2I"
+BMGC_DS19653,BMG_DS075890,"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 15"
+BMGC_DS19654,BMG_DS075894,MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY 2 WITH MYOPATHY AND NEUROPATHY
+BMGC_DS19655,BMG_DS075898,central core myopathy
+BMGC_DS19656,BMG_DS075901,MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY 1 WITH MYOPATHY AND NEUROPATHY
+BMGC_DS19657,BMG_DS075960,Autosomal dominant popliteal pterygium syndrome
+BMGC_DS19658,BMG_DS075964,"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA"
+BMGC_DS19659,BMG_DS075985,Deficiency of hypoxanthine phosphoribosyltransferase
+BMGC_DS19660,BMG_DS075988,Resistance to activated protein C due to factor V Leiden mutation
+BMGC_DS19661,BMG_DS075991,MYOCLONIC EPILEPSY OF LAFORA 1
+BMGC_DS19662,BMG_DS075996,Lamellar ichthyosis (disorder)
+BMGC_DS19663,BMG_DS075998,Secondary polycythemia
+BMGC_DS19664,BMG_DS075999,Hemophilia B Leyden
+BMGC_DS19665,BMG_DS076000,Primary adrenocortical insufficiency
+BMGC_DS19666,BMG_DS076002,"Spinal Muscular Atrophy, Infantile"
+BMGC_DS19667,BMG_DS076004,Hearing Disorders
+BMGC_DS19668,BMG_DS076011,Porphyria (disorder)
+BMGC_DS19669,BMG_DS076012,Porphyrias
+BMGC_DS19670,BMG_DS076015,DYSTONIA-DEAFNESS SYNDROME 1
+BMGC_DS19671,BMG_DS076020,Myotonia permanens
+BMGC_DS19672,BMG_DS076029,"IMMUNE DYSREGULATION, AUTOIMMUNITY, AND AUTOINFLAMMATION"
+BMGC_DS19673,BMG_DS076030,"BECKER NEVUS, ISOLATED"
+BMGC_DS19674,BMG_DS076031,"HYPER-IgE SYNDROME 6, AUTOSOMAL DOMINANT, WITH RECURRENT INFECTIONS"
+BMGC_DS19675,BMG_DS076075,B-lymphoblastic leukemia with MYC rearrangement
+BMGC_DS19676,BMG_DS076077,B-lymphoblastic leukemia with MEF2D rearrangement
+BMGC_DS19677,BMG_DS076078,B-lymphoblastic leukemia with ZNF384 rearrangement
+BMGC_DS19678,BMG_DS076079,B-lymphoblastic leukemia with NUTM1 rearrangement
+BMGC_DS19679,BMG_DS076081,B-lymphoblastic leukemia with PAX5alt
+BMGC_DS19680,BMG_DS076082,acute myeloid leukemia with FUS-ERG fusion
+BMGC_DS19681,BMG_DS076083,acute myeloid leukemia with NPM1-MLF1 fusion
+BMGC_DS19682,BMG_DS076084,B-lymphoblastic leukemia with TCF3-HLF fusion
+BMGC_DS19683,BMG_DS076421,"ALPORT SYNDROME 3A, AUTOSOMAL DOMINANT"
+BMGC_DS19684,BMG_DS076422,LUI-JEE-BARON SYNDROME
+BMGC_DS19685,BMG_DS076423,IMMUNODEFICIENCY 118
+BMGC_DS19686,BMG_DS076424,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 113"
+BMGC_DS19687,BMG_DS076425,"AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL, 1"
+BMGC_DS19688,BMG_DS076426,TUMOR PREDISPOSITION SYNDROME 4
+BMGC_DS19689,BMG_DS076427,"SPASTIC PARAPLEGIA 72A, AUTOSOMAL DOMINANT"
+BMGC_DS19690,BMG_DS076428,"EPILEPSY, EARLY-ONSET, 2, WITH OR WITHOUT DEVELOPMENTAL DELAY"
+BMGC_DS19691,BMG_DS076429,"EPIDERMOLYTIC HYPERKERATOSIS 2A, AUTOSOMAL DOMINANT"
+BMGC_DS19692,BMG_DS076430,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL RECESSIVE 9"
+BMGC_DS19693,BMG_DS076431,"encephalitis, acute, infection-induced, susceptibility to, 12"
+BMGC_DS19694,BMG_DS076432,"EPILEPSY, EARLY-ONSET, 3, WITH OR WITHOUT DEVELOPMENTAL DELAY"
+BMGC_DS19695,BMG_DS076433,"CRANIAL DYSINNERVATION DISORDER, CONGENITAL, WITH ABSENT CORNEAL REFLEX AND DEVELOPMENTAL DELAY"
+BMGC_DS19696,BMG_DS076434,"congenital smooth muscle hamartoma, with or without hemihypertrophy"
+BMGC_DS19697,BMG_DS076435,"THROMBOCYTOPENIA 8, WITH DYSMORPHIC FEATURES AND DEVELOPMENTAL DELAY"
+BMGC_DS19698,BMG_DS076436,THROMBOCYTOPENIA 9
+BMGC_DS19699,BMG_DS076437,"AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL, 2"
+BMGC_DS19700,BMG_DS076438,"PARKINSON DISEASE 25, AUTOSOMAL RECESSIVE EARLY-ONSET, WITH IMPAIRED INTELLECTUAL DEVELOPMENT"
+BMGC_DS19701,BMG_DS076439,"VARIEGATE PORPHYRIA, CHILDHOOD-ONSET"
+BMGC_DS19702,BMG_DS076440,THROMBOCYTOPENIA 10
+BMGC_DS19703,BMG_DS076441,"BLEEDING DISORDER, PLATELET-TYPE, 25"
+BMGC_DS19704,BMG_DS076442,NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES
+BMGC_DS19705,BMG_DS076443,SPERMATOGENIC FAILURE 85
+BMGC_DS19706,BMG_DS076444,"NEURODEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE, BEHAVIORAL ABNORMALITIES, AND DYSMORPHIC FACIES"
+BMGC_DS19707,BMG_DS076445,SPERMATOGENIC FAILURE 87
+BMGC_DS19708,BMG_DS076446,ZIEGLER-HUANG SYNDROME
+BMGC_DS19709,BMG_DS076447,NEURODEVELOPMENTAL DISORDER WITH LANGUAGE DELAY AND VARIABLE COGNITIVE ABNORMALITIES
+BMGC_DS19710,BMG_DS076448,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 111
+BMGC_DS19711,BMG_DS076449,ICHTHYOSIS WITH ERYTHROKERATODERMA
+BMGC_DS19712,BMG_DS076450,XEROSIS AND GROWTH FAILURE WITH IMMUNE AND PULMONARY DYSFUNCTION SYNDROME
+BMGC_DS19713,BMG_DS076451,FLIEDNER-ZWEIER SYNDROME
+BMGC_DS19714,BMG_DS076452,"SPASTIC PARAPLEGIA 18A, AUTOSOMAL DOMINANT"
+BMGC_DS19715,BMG_DS076453,"NEURODEVELOPMENTAL DISORDER WITH MOTOR REGRESSION, PROGRESSIVE SPASTIC PARAPLEGIA, AND OROMOTOR DYSFUNCTION"
+BMGC_DS19716,BMG_DS076454,ARRHYTHMOGENIC CARDIOMYOPATHY WITH VARIABLE ECTODERMAL ABNORMALITIES
+BMGC_DS19717,BMG_DS076455,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 11"
+BMGC_DS19718,BMG_DS076456,"DEVELOPMENTAL DELAY, DYSMORPHIC FACIES, AND BRAIN ANOMALIES"
+BMGC_DS19719,BMG_DS076457,"ALPORT SYNDROME 3B, AUTOSOMAL RECESSIVE"
+BMGC_DS19720,BMG_DS076458,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 112
+BMGC_DS19721,BMG_DS076459,"SPASTIC PARAPLEGIA 91, AUTOSOMAL DOMINANT, WITH OR WITHOUT CEREBELLAR ATAXIA"
+BMGC_DS19722,BMG_DS076460,DEVELOPMENTAL DELAY WITH OR WITHOUT EPILEPSY
+BMGC_DS19723,BMG_DS076461,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL RECESSIVE 10"
+BMGC_DS19724,BMG_DS076462,"ARTHROGRYPOSIS, DISTAL, TYPE 12"
+BMGC_DS19725,BMG_DS076463,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIbb"
+BMGC_DS19726,BMG_DS076464,SPERMATOGENIC FAILURE 88
+BMGC_DS19727,BMG_DS076465,PREMATURE OVARIAN FAILURE 22
+BMGC_DS19728,BMG_DS076466,OPTIC ATROPHY 14
+BMGC_DS19729,BMG_DS076467,"DEAFNESS, AUTOSOMAL RECESSIVE 121"
+BMGC_DS19730,BMG_DS076468,CRANIOMETADIAPHYSEAL OSTEOSCLEROSIS WITH HIP DYSPLASIA
+BMGC_DS19731,BMG_DS076469,IMMUNODEFICIENCY 113 WITH AUTOIMMUNITY AND AUTOINFLAMMATION
+BMGC_DS19732,BMG_DS076470,CORNELIA DE LANGE SYNDROME 6
+BMGC_DS19733,BMG_DS076471,"LEBER-LIKE HEREDITARY OPTIC NEUROPATHY, AUTOSOMAL RECESSIVE 2"
+BMGC_DS19734,BMG_DS076472,"CILIARY DYSKINESIA, PRIMARY, 52"
+BMGC_DS19735,BMG_DS076473,OTOSCLEROSIS 11
+BMGC_DS19736,BMG_DS076474,OPTIC ATROPHY 15
+BMGC_DS19737,BMG_DS076475,GARG-MISHRA PROGEROID SYNDROME
+BMGC_DS19738,BMG_DS076476,lymphatic malformation 14
+BMGC_DS19739,BMG_DS076477,"IMMUNODEFICIENCY 114, FOLATE-RESPONSIVE"
+BMGC_DS19740,BMG_DS076478,"SPASTIC PARAPLEGIA 72B, AUTOSOMAL RECESSIVE"
+BMGC_DS19741,BMG_DS076479,LONG-OLSEN-DISTELMAIER SYNDROME
+BMGC_DS19742,BMG_DS076480,OOCYTE/ZYGOTE/EMBRYO MATURATION ARREST 21
+BMGC_DS19743,BMG_DS076481,OPTIC ATROPHY 16
+BMGC_DS19744,BMG_DS076482,IMMUNODEFICIENCY 115 WITH AUTOINFLAMMATION
+BMGC_DS19745,BMG_DS076483,"CARDIOMYOPATHY, DILATED, 2J"
+BMGC_DS19746,BMG_DS076484,"NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATAXIA AND COGNITIVE DECLINE"
+BMGC_DS19747,BMG_DS076485,TAN-ALMURSHEDI SYNDROME
+BMGC_DS19748,BMG_DS076486,"CILIARY DYSKINESIA, PRIMARY, 53"
+BMGC_DS19749,BMG_DS076487,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 59
+BMGC_DS19750,BMG_DS076488,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 6"
+BMGC_DS19751,BMG_DS076489,"DIABETES, DEAFNESS, DEVELOPMENTAL DELAY, AND SHORT STATURE SYNDROME"
+BMGC_DS19752,BMG_DS076490,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 80, WITH VARIANT LISSENCEPHALY"
+BMGC_DS19753,BMG_DS076491,THROMBOCYTOPENIA 11 WITH MULTIPLE CONGENITAL ANOMALIES AND DYSMORPHIC FACIES
+BMGC_DS19754,BMG_DS076492,ALFADHEL SYNDROME
+BMGC_DS19755,BMG_DS076493,HOXHA-ALIU SYNDROME
+BMGC_DS19756,BMG_DS076494,"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GUO-CAMPEAU TYPE"
+BMGC_DS19757,BMG_DS076495,"SPASTIC ATAXIA 10, AUTOSOMAL RECESSIVE"
+BMGC_DS19758,BMG_DS076496,IMMUNODEFICIENCY 117
+BMGC_DS19759,BMG_DS076497,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 9
+BMGC_DS19760,BMG_DS076498,"IMMUNODEFICIENCY, COMMON VARIABLE, 15"
+BMGC_DS19761,BMG_DS076499,"NEUTROPENIA, SEVERE CONGENITAL, 11, AUTOSOMAL DOMINANT"
+BMGC_DS19762,BMG_DS076500,"LEUKODYSTROPHY, HYPOMYELINATING, 27"
+BMGC_DS19763,BMG_DS076501,"LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 8"
+BMGC_DS19764,BMG_DS076502,"LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 5"
+BMGC_DS19765,BMG_DS076503,"LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 9"
+BMGC_DS19766,BMG_DS076504,PREMATURE OVARIAN FAILURE 23
+BMGC_DS19767,BMG_DS076505,MOYAMOYA DISEASE 7
+BMGC_DS19768,BMG_DS076506,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 74"
+BMGC_DS19769,BMG_DS076507,DEVELOPMENTAL DYSPLASIA OF THE HIP 3
+BMGC_DS19770,BMG_DS076508,YUKSEL-VOGEL-BAUER SYNDROME
+BMGC_DS19771,BMG_DS076509,SPERMATOGENIC FAILURE 89
+BMGC_DS19772,BMG_DS076510,"EPIDERMOLYTIC HYPERKERATOSIS 2B, AUTOSOMAL RECESSIVE"
+BMGC_DS19773,BMG_DS076511,POLYDACTYLY-MACROCEPHALY SYNDROME
+BMGC_DS19774,BMG_DS076512,SPERMATOGENIC FAILURE 86
+BMGC_DS19775,BMG_DS076513,"NEUTROPENIA, SEVERE CONGENITAL, 10, AUTOSOMAL RECESSIVE"
+BMGC_DS19776,BMG_DS076514,"OSTEOGENESIS IMPERFECTA, TYPE XXIII"
+BMGC_DS19777,BMG_DS076515,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 81"
+BMGC_DS19778,BMG_DS076542,"AMELOGENESIS IMPERFECTA, TYPE IIIA"
+BMGC_DS19779,BMG_DS076544,"Porphyria, Erythropoietic, Congenital"
+BMGC_DS19780,BMG_DS076545,MICROPHTHALMIA/COLOBOMA 12
+BMGC_DS19781,BMG_DS076555,Listeria monocytogenes Infections
+BMGC_DS19782,BMG_DS076568,"HYPERTRICHOSIS, CONGENITAL GENERALIZED, 2"
+BMGC_DS19783,BMG_DS076569,"GROWTH HORMONE DEFICIENCY, ISOLATED PARTIAL"
+BMGC_DS19784,BMG_DS076573,SPINOCEREBELLAR ATAXIA 47
+BMGC_DS19785,BMG_DS076574,AURONEURODENTAL SYNDROME
+BMGC_DS19786,BMG_DS076576,"hyperemesis gravidarum, susceptibility to"
+BMGC_DS19787,BMG_DS076577,"Albinism, Partial"
+BMGC_DS19788,BMG_DS076578,Blastomyces dermatitidis Infection
+BMGC_DS19789,BMG_DS077374,"ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1A/1B, DIGENIC"
+BMGC_DS19790,BMG_DS077375,"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 37"
+BMGC_DS19791,BMG_DS077376,"SPERMATOGENIC FAILURE, X-LINKED, 8"
+BMGC_DS19792,BMG_DS077377,"prostate cancer, hereditary, X-linked 3"
+BMGC_DS19793,BMG_DS077378,"SPASTIC PARAPLEGIA 30B, AUTOSOMAL RECESSIVE"
+BMGC_DS19794,BMG_DS077379,"AMYLOIDOSIS, HEREDITARY SYSTEMIC 5"
+BMGC_DS19795,BMG_DS077380,"AMYLOIDOSIS, HEREDITARY SYSTEMIC 6"
+BMGC_DS19796,BMG_DS077381,"ENCEPHALOPATHY, PORPHYRIA-RELATED"
+BMGC_DS19797,BMG_DS077382,"LEUKOENCEPHALOPATHY, PORPHYRIA-RELATED"
+BMGC_DS19798,BMG_DS077383,"DEAFNESS, AUTOSOMAL RECESSIVE 122"
+BMGC_DS19799,BMG_DS077384,"BLEEDING DISORDER, VASCULAR-TYPE"
+BMGC_DS19800,BMG_DS077385,OROFACIODIGITAL SYNDROME XX
+BMGC_DS19801,BMG_DS077386,"DEAFNESS, AUTOSOMAL DOMINANT 90"
+BMGC_DS19802,BMG_DS077387,BETHLEM MYOPATHY 1B
+BMGC_DS19803,BMG_DS077388,BETHLEM MYOPATHY 1C
+BMGC_DS19804,BMG_DS077389,ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1B
+BMGC_DS19805,BMG_DS077390,ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1C
+BMGC_DS19806,BMG_DS077391,MICROPHTHALMIA/COLOBOMA 11
+BMGC_DS19807,BMG_DS077392,"NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS, SEIZURES, AND STRUCTURAL BRAIN ABNORMALITIES"
+BMGC_DS19808,BMG_DS077393,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 30, ATRIAL"
+BMGC_DS19809,BMG_DS077394,SPERMATOGENIC FAILURE 90
+BMGC_DS19810,BMG_DS077395,"DEAFNESS, AUTOSOMAL RECESSIVE 123"
+BMGC_DS19811,BMG_DS077396,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CHARACTERISTIC BRAIN ABNORMALITIES
+BMGC_DS19812,BMG_DS077397,NEURODEVELOPMENTAL DISORDER WITH EARLY-ONSET PARKINSONISM AND BEHAVIORAL ABNORMALITIES
+BMGC_DS19813,BMG_DS077398,MEGALENCEPHALY-POLYDACTYLY SYNDROME
+BMGC_DS19814,BMG_DS077399,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 12"
+BMGC_DS19815,BMG_DS077400,THROMBOCYTOPENIA 12 WITH OR WITHOUT MYOPATHY
+BMGC_DS19816,BMG_DS077401,MACULAR DYSTROPHY WITH OR WITHOUT CONE DYSFUNCTION
+BMGC_DS19817,BMG_DS077402,SECKEL SYNDROME 11
+BMGC_DS19818,BMG_DS077403,JEFFRIES-LAKHANI NEURODEVELOPMENTAL SYNDROME
+BMGC_DS19819,BMG_DS077404,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 113
+BMGC_DS19820,BMG_DS077405,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 114
+BMGC_DS19821,BMG_DS077406,"THROMBOCYTOPENIA 13, SYNDROMIC"
+BMGC_DS19822,BMG_DS077407,"PULMONARY HYPERTENSION, PRIMARY, 6"
+BMGC_DS19823,BMG_DS077408,"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 82"
+BMGC_DS19824,BMG_DS077409,"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE ID"
+BMGC_DS19825,BMG_DS077410,"NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT, AUTISM, AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER"
+BMGC_DS19826,BMG_DS077411,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 115
+BMGC_DS19827,BMG_DS077412,NEURODEVELOPMENTAL DISORDER PLUS OPTIC ATROPHY
+BMGC_DS19828,BMG_DS077413,NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MOVEMENT ABNORMALITIES
+BMGC_DS19829,BMG_DS077414,"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 9, AUTOSOMAL RECESSIVE"
+BMGC_DS19830,BMG_DS077415,APLASIA CUTIS-ENAMEL DYSPLASIA SYNDROME
+BMGC_DS19831,BMG_DS077416,NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND SEIZURES
+BMGC_DS19832,BMG_DS077417,OTOSCLEROSIS 12
+BMGC_DS19833,BMG_DS077418,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 29"
+BMGC_DS19834,BMG_DS077419,"DEAFNESS, AUTOSOMAL RECESSIVE 124"
+BMGC_DS19835,BMG_DS077420,AUTOINFLAMMATION WITH EPISODIC FEVER AND IMMUNE DYSREGULATION
+BMGC_DS19836,BMG_DS077421,PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 6
+BMGC_DS19837,BMG_DS077422,DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 116
+BMGC_DS19838,BMG_DS077423,IMMUNODEFICIENCY 121 WITH AUTOINFLAMMATION
+BMGC_DS19839,BMG_DS077424,MHC CLASS I DEFICIENCY 2
+BMGC_DS19840,BMG_DS077425,MHC CLASS I DEFICIENCY 3
+BMGC_DS19841,BMG_DS077426,"ROTHMUND-THOMSON SYNDROME, TYPE 4"
+BMGC_DS19842,BMG_DS077427,EL HAYEK-CHAHROUR NEURODEVELOPMENTAL SYNDROME
+BMGC_DS19843,BMG_DS077428,IMMUNODEFICIENCY 119
+BMGC_DS19844,BMG_DS077429,IMMUNODEFICIENCY 120
+BMGC_DS19845,BMG_DS077430,SPERMATOGENIC FAILURE 91
+BMGC_DS19846,BMG_DS077431,PREMATURE OVARIAN FAILURE 24
+BMGC_DS19847,BMG_DS077432,SPERMATOGENIC FAILURE 92
+BMGC_DS19848,BMG_DS077433,SPERMATOGENIC FAILURE 93
+BMGC_DS19849,BMG_DS077434,SPERMATOGENIC FAILURE 94
+BMGC_DS19850,BMG_DS077435,"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"
+BMGC_DS19852,BMG_DS077437,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL RECESSIVE 11, WITH SPASTICITY"
+BMGC_DS19853,BMG_DS077438,"EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 3"
+BMGC_DS19854,BMG_DS077439,IMMUNODEFICIENCY 122
+BMGC_DS19855,BMG_DS077440,"DEAFNESS, AUTOSOMAL RECESSIVE 125"
+BMGC_DS19856,BMG_DS077441,AUTOINFLAMMATION WITH ARTHRITIS AND VASCULITIS
+BMGC_DS19857,BMG_DS077442,MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 9B
+BMGC_DS19858,BMG_DS077443,"CARDIOMYOPATHY, DILATED, 2K"
+BMGC_DS19859,BMG_DS077444,OVARIAN DYSGENESIS 11
+BMGC_DS19860,BMG_DS077445,IMMUNODEFICIENCY 123 WITH HPV-RELATED VERRUCOSIS
+BMGC_DS19861,BMG_DS077446,POLYCYSTIC KIDNEY DISEASE 8
+BMGC_DS19862,BMG_DS077447,ARTERIAL TORTUOSITY-BONE FRAGILITY SYNDROME
+BMGC_DS19863,BMG_DS077448,OTOFACIAL NEURODEVELOPMENTAL SYNDROME
+BMGC_DS19864,BMG_DS077449,"NEUROMUSCULAR DISORDER, CONGENITAL, WITH DYSMORPHIC FACIES"
+BMGC_DS19865,BMG_DS077473,SPINAL MUSCULAR ATROPHY WITH MICROCEPHALY AND IMPAIRED INTELLECTUAL DEVELOPMENT
+BMGC_DS19866,BMG_DS077478,Plica polonica
+BMGC_DS19867,BMG_DS077479,ASM Deficiency
+BMGC_DS19868,BMG_DS077480,Fulminant Intracranial Hypertension
+BMGC_DS19869,BMG_DS077481,Secondary Intracranial Hypertension
+BMGC_DS19870,BMG_DS077485,myofibrillar myopathy 3
+BMGC_DS19871,BMG_DS077486,tinea barbae
+BMGC_DS19872,BMG_DS077488,Rapp-Hodgkin syndrome
+BMGC_DS19873,BMG_DS077489,chromosome 5q deletion syndrome
+BMGC_DS19874,BMG_DS077490,distal arthrogryposis type 1A
+BMGC_DS19875,BMG_DS077491,Bethlem myopathy
+BMGC_DS19876,BMG_DS077492,Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency
+BMGC_DS19877,BMG_DS077494,cardiofaciocutaneous syndrome
+BMGC_DS19878,BMG_DS077495,NFIA-related disorder
+BMGC_DS19879,BMG_DS077496,Doyne honeycomb retinal dystrophy
+BMGC_DS19880,BMG_DS077497,"acromesomelic dysplasia, Maroteaux type"
+BMGC_DS19881,BMG_DS077498,adrenocorticotropic hormone deficiency
+BMGC_DS19882,BMG_DS077499,rigid spine syndrome
+BMGC_DS19883,BMG_DS077500,spondyloepiphyseal dysplasia congenita
+BMGC_DS19884,BMG_DS077501,deafness-dystonia-optic neuronopathy syndrome
+BMGC_DS19885,BMG_DS077502,molybdenum cofactor deficiency
+BMGC_DS19886,BMG_DS077503,pseudoachondroplasia
+BMGC_DS19887,BMG_DS077504,distal arthrogryposis type 7
+BMGC_DS19888,BMG_DS077505,myofibrillar myopathy 3
+BMGC_DS19889,BMG_DS077508,achondrogenesis type II
+BMGC_DS19890,BMG_DS077509,medium chain acyl-CoA dehydrogenase deficiency
+BMGC_DS19891,BMG_DS077510,"Mycobacterium tuberculosis, susceptibility"
+BMGC_DS19892,BMG_DS077511,"Ehlers-Danlos syndrome, spondylodysplastic type"
+BMGC_DS19893,BMG_DS077512,congenital central hypoventilation syndrome
+BMGC_DS19894,BMG_DS077513,Joubert syndrome 2
+BMGC_DS19895,BMG_DS077514,Joubert syndrome 3
+BMGC_DS19896,BMG_DS077515,nonsyndromic congenital nail disorder 4
+BMGC_DS19897,BMG_DS077516,Waardenburg syndrome type 2A
+BMGC_DS19898,BMG_DS077517,fetal akinesia deformation sequence
+BMGC_DS19899,BMG_DS077518,Winchester syndrome
+BMGC_DS19900,BMG_DS077519,Charlevoix-Saguenay spastic ataxia
+BMGC_DS19901,BMG_DS077520,glutaric acidemia I
+BMGC_DS19902,BMG_DS077521,familial medullary thyroid carcinoma
+BMGC_DS19903,BMG_DS077522,arrhythmogenic right ventricular dysplasia 1
+BMGC_DS19904,BMG_DS077523,Townes-Brocks syndrome
+BMGC_DS19905,BMG_DS077524,Allan-Herndon-Dudley syndrome
+BMGC_DS19906,BMG_DS077525,brachydactyly type A3
+BMGC_DS19907,BMG_DS077526,Brown-Vialetto-Van Laere syndrome
+BMGC_DS19908,BMG_DS077527,Noonan syndrome with multiple lentigines 2
+BMGC_DS19909,BMG_DS077528,spinocerebellar ataxia type 26
+BMGC_DS19910,BMG_DS077529,formaldehyde poisoning
+BMGC_DS19911,BMG_DS077530,distal arthrogryposis type 3
+BMGC_DS19912,BMG_DS077533,sinonasal undifferentiated carcinoma
+BMGC_DS19913,BMG_DS077534,methylmalonic aciduria and homocystinuria
+BMGC_DS19914,BMG_DS077535,"contractures, pterygia, and spondylocarpotarsal fusion syndrome"
+BMGC_DS19915,BMG_DS077536,linear skin defects with multiple congenital anomalies
+BMGC_DS19916,BMG_DS077537,Seckel syndrome 2
+BMGC_DS19917,BMG_DS077539,microcephalic osteodysplastic primordial dwarfism type I
+BMGC_DS19918,BMG_DS077540,biotin-responsive basal ganglia disease
+BMGC_DS19919,BMG_DS077541,Joubert syndrome 5
+BMGC_DS19920,BMG_DS077542,Joubert syndrome 6
+BMGC_DS19921,BMG_DS077543,Hermansky-Pudlak syndrome 2
+BMGC_DS19922,BMG_DS077546,Noonan syndrome 3
+BMGC_DS19923,BMG_DS077547,spinocerebellar ataxia 27A
+BMGC_DS19924,BMG_DS077549,Peters anomaly
+BMGC_DS19925,BMG_DS077550,lattice corneal dystrophy
+BMGC_DS19926,BMG_DS077551,dystonia 12
+BMGC_DS19927,BMG_DS077553,frontonasal dysplasia
+BMGC_DS19928,BMG_DS077554,non-syndromic synpolydactyly
+BMGC_DS19929,BMG_DS077555,Blau syndrome
+BMGC_DS19930,BMG_DS077557,retinitis pigmentosa 1
+BMGC_DS19931,BMG_DS077558,nemaline myopathy 5A
+BMGC_DS19932,BMG_DS077559,distal arthrogryposis type 2B
+BMGC_DS19933,BMG_DS077560,obsolete childhood hypophosphatasia
+BMGC_DS19934,BMG_DS077563,lymphoid interstitial pneumonia
+BMGC_DS19935,BMG_DS077566,cerebellar hypoplasia
+BMGC_DS19936,BMG_DS077567,epidermolysis bullosa with congenital localized absence of skin and deformity of nails
+BMGC_DS19937,BMG_DS077568,Aland Island eye disease
+BMGC_DS19938,BMG_DS077569,inherited prekallikrein deficiency
+BMGC_DS19939,BMG_DS077571,3-methylglutaconic aciduria type 1
+BMGC_DS19940,BMG_DS077572,craniodiaphyseal dysplasia
+BMGC_DS19941,BMG_DS077573,cleft soft palate
+BMGC_DS19942,BMG_DS077574,cranioectodermal dysplasia
+BMGC_DS19943,BMG_DS077575,hypochondrogenesis
+BMGC_DS19944,BMG_DS077576,preterm premature rupture of the membranes
+BMGC_DS19945,BMG_DS077577,basal laminar drusen
+BMGC_DS19946,BMG_DS077578,pigment dispersion syndrome
+BMGC_DS19947,BMG_DS077579,thyroid dyshormonogenesis 2A
+BMGC_DS19948,BMG_DS077580,renal agenesis
+BMGC_DS19949,BMG_DS077581,inflammatory bowel disease 2
+BMGC_DS19950,BMG_DS077582,obsolete autosomal dominant limb-girdle muscular dystrophy type 1C
+BMGC_DS19951,BMG_DS077583,Cayman type cerebellar ataxia
+BMGC_DS19952,BMG_DS077584,orofacial cleft 3
+BMGC_DS19953,BMG_DS077585,orofacial cleft 7
+BMGC_DS19954,BMG_DS077586,inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+BMGC_DS19955,BMG_DS077587,chromosome 17q11.2 deletion syndrome
+BMGC_DS19956,BMG_DS077588,retinitis pigmentosa 27
+BMGC_DS19957,BMG_DS077589,holoprosencephaly 7
+BMGC_DS19958,BMG_DS077590,orofacial cleft 5
+BMGC_DS19959,BMG_DS077591,inflammatory bowel disease 9
+BMGC_DS19960,BMG_DS077592,"hyper-IgE recurrent infection syndrome 1, autosomal dominant"
+BMGC_DS19961,BMG_DS077593,Leber congenital amaurosis 11
+BMGC_DS19962,BMG_DS077595,holoprosencephaly 3
+BMGC_DS19963,BMG_DS077596,achromatopsia 4
+BMGC_DS19964,BMG_DS077597,retinitis pigmentosa 30
+BMGC_DS19965,BMG_DS077598,hypotrichosis-lymphedema-telangiectasia syndrome
+BMGC_DS19966,BMG_DS077599,combined deficiency of vitamin K-dependent clotting factors 2
+BMGC_DS19967,BMG_DS077600,obsolete inherited genitourinary tract anomalies
+BMGC_DS19968,BMG_DS077601,retinitis pigmentosa 3
+BMGC_DS19969,BMG_DS077602,Uruguay faciocardiomusculoskeletal syndrome
+BMGC_DS19970,BMG_DS077604,cone-rod dystrophy 10
+BMGC_DS19971,BMG_DS077605,nephronophthisis 4
+BMGC_DS19972,BMG_DS077606,Carney-Stratakis syndrome
+BMGC_DS19973,BMG_DS077607,inflammatory bowel disease 4
+BMGC_DS19974,BMG_DS077608,inflammatory bowel disease 6
+BMGC_DS19975,BMG_DS077609,inflammatory bowel disease 8
+BMGC_DS19976,BMG_DS077610,congenital nonspherocytic hemolytic anemia 2
+BMGC_DS19977,BMG_DS077612,obsoleted echo virus 11 sensitivity
+BMGC_DS19978,BMG_DS077613,keratosis palmoplantaris striata 2
+BMGC_DS19979,BMG_DS077614,complement component 4a deficiency
+BMGC_DS19980,BMG_DS077615,cerebrooculofacioskeletal syndrome 4
+BMGC_DS19981,BMG_DS077616,brachydactyly-syndactyly syndrome
+BMGC_DS19982,BMG_DS077617,retinitis pigmentosa 35
+BMGC_DS19983,BMG_DS077618,inflammatory bowel disease 5
+BMGC_DS19984,BMG_DS077619,exudative vitreoretinopathy 3
+BMGC_DS19985,BMG_DS077621,macrocephaly-autism syndrome
+BMGC_DS19986,BMG_DS077622,inflammatory bowel disease 7
+BMGC_DS19987,BMG_DS077623,Mast syndrome
+BMGC_DS19988,BMG_DS077624,hydrolethalus syndrome 1
+BMGC_DS19989,BMG_DS077625,Friedreich ataxia 1
+BMGC_DS19990,BMG_DS077627,Wolfram syndrome 2
+BMGC_DS19991,BMG_DS077628,Bardet-Biedl syndrome 6
+BMGC_DS19992,BMG_DS077629,inflammatory bowel disease 3
+BMGC_DS19993,BMG_DS077630,nephronophthisis 3
+BMGC_DS19994,BMG_DS077631,focal segmental glomerulosclerosis 2
+BMGC_DS19995,BMG_DS077632,long QT syndrome 3
+BMGC_DS19996,BMG_DS077633,Bardet-Biedl syndrome 7
+BMGC_DS19997,BMG_DS077634,Bardet-Biedl syndrome 8
+BMGC_DS19998,BMG_DS077635,Bardet-Biedl syndrome 9
+BMGC_DS19999,BMG_DS077636,Bardet-Biedl syndrome 10
+BMGC_DS20000,BMG_DS077637,Bardet-Biedl syndrome 11
+BMGC_DS20001,BMG_DS077638,Bardet-Biedl syndrome 12
+BMGC_DS20002,BMG_DS077639,atrichia with papular lesions
+BMGC_DS20003,BMG_DS077640,arterial tortuosity syndrome
+BMGC_DS20004,BMG_DS077642,distal arthrogryposis type 10
+BMGC_DS20005,BMG_DS077643,orofacial cleft 1
+BMGC_DS20006,BMG_DS077644,acromelic frontonasal dysostosis
+BMGC_DS20007,BMG_DS077645,orofacial cleft 2
+BMGC_DS20008,BMG_DS077646,retinitis pigmentosa 36
+BMGC_DS20009,BMG_DS077647,holoprosencephaly 5
+BMGC_DS20010,BMG_DS077648,retinal cone dystrophy 4
+BMGC_DS20011,BMG_DS077649,nephronophthisis 2
+BMGC_DS20012,BMG_DS077650,Friedreich ataxia 2
+BMGC_DS20013,BMG_DS077651,orofacial cleft 10
+BMGC_DS20014,BMG_DS077652,retinitis pigmentosa 19
+BMGC_DS20015,BMG_DS077653,retinitis pigmentosa 9
+BMGC_DS20016,BMG_DS077654,retinal cone dystrophy 1
+BMGC_DS20017,BMG_DS077656,familial pterygium of the conjunctiva
+BMGC_DS20018,BMG_DS077657,long QT syndrome 5
+BMGC_DS20019,BMG_DS077658,Char syndrome
+BMGC_DS20020,BMG_DS077659,parietal foramina
+BMGC_DS20021,BMG_DS077660,CAKUT
+BMGC_DS20022,BMG_DS077661,Joubert syndrome 7
+BMGC_DS20023,BMG_DS077662,nephronophthisis 7
+BMGC_DS20024,BMG_DS077663,multiple endocrine neoplasia type 4
+BMGC_DS20025,BMG_DS077664,warfarin sensitivity
+BMGC_DS20026,BMG_DS077665,Bardet-Biedl syndrome 13
+BMGC_DS20027,BMG_DS077667,Leber congenital amaurosis 13
+BMGC_DS20028,BMG_DS077668,orofacial cleft 11
+BMGC_DS20029,BMG_DS077669,dystonia 16
+BMGC_DS20030,BMG_DS077670,bestrophinopathy
+BMGC_DS20031,BMG_DS077672,"spondyloepimetaphyseal dysplasia, Pakistani type"
+BMGC_DS20032,BMG_DS077673,mitochondrial DNA depletion syndrome 5
+BMGC_DS20033,BMG_DS077674,Parkinson's disease 14
+BMGC_DS20034,BMG_DS077675,retinitis pigmentosa 42
+BMGC_DS20035,BMG_DS077676,"46,XY sex reversal 4"
+BMGC_DS20036,BMG_DS077677,inhalation anthrax
+BMGC_DS20037,BMG_DS077679,achondrogenesis
+BMGC_DS20038,BMG_DS077680,frontotemporal dementia and/or amyotrophic lateral sclerosis 7
+BMGC_DS20039,BMG_DS077682,immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
+BMGC_DS20040,BMG_DS077683,Larsen syndrome
+BMGC_DS20041,BMG_DS077684,mitochondrial DNA depletion syndrome 5
+BMGC_DS20042,BMG_DS077686,"Abdomen, Acute"
+BMGC_DS20043,BMG_DS077688,Abdominal Neoplasms
+BMGC_DS20044,BMG_DS077689,obsolete congenital abnormality
+BMGC_DS20045,BMG_DS077690,"Abnormalities, Drug-Induced"
+BMGC_DS20046,BMG_DS077691,"Abnormalities, Multiple"
+BMGC_DS20047,BMG_DS077693,"Abortion, Spontaneous"
+BMGC_DS20048,BMG_DS077697,"Abortion, Threatened"
+BMGC_DS20049,BMG_DS077698,Abruptio Placentae
+BMGC_DS20050,BMG_DS077708,autism spectrum disorder
+BMGC_DS20051,BMG_DS077723,Anterior Cruciate Ligament Injuries
+BMGC_DS20052,BMG_DS077729,"Brain Injuries, Diffuse"
+BMGC_DS20053,BMG_DS077731,"Brain Injuries, Traumatic"
+BMGC_DS20054,BMG_DS077735,hyperekplexia | hyperekplexia 1
+BMGC_DS20055,BMG_DS077736,Anorectal Malformations
+BMGC_DS20056,BMG_DS077752,ST-elevation myocardial infarction
+BMGC_DS20057,BMG_DS077753,Ciliopathies
+BMGC_DS20058,BMG_DS077756,ankyloglossia
+BMGC_DS20059,BMG_DS077757,Cancer Pain
+BMGC_DS20060,BMG_DS077768,Meconium Ileus
+BMGC_DS20061,BMG_DS077769,Opium Dependence
+BMGC_DS20062,BMG_DS077773,Cardiac Conduction System Disease
+BMGC_DS20063,BMG_DS077774,heavy metal poisoning
+BMGC_DS20064,BMG_DS077775,immunoglobulin light chain amyloidosis
+BMGC_DS20065,BMG_DS077778,Clinical Deterioration
+BMGC_DS20066,BMG_DS077780,Drug Misuse
+BMGC_DS20067,BMG_DS077782,Adenocarcinoma of Lung
+BMGC_DS20068,BMG_DS077783,Squamous Cell Carcinoma of Head and Neck
+BMGC_DS20069,BMG_DS077785,"Carcinoma, Ovarian Epithelial"
+BMGC_DS20070,BMG_DS077786,Sleepiness
+BMGC_DS20071,BMG_DS077787,"Thyroid Cancer, Papillary"
+BMGC_DS20072,BMG_DS077788,Nasopharyngeal Carcinoma
+BMGC_DS20073,BMG_DS077789,Esophageal Squamous Cell Carcinoma
+BMGC_DS20074,BMG_DS077793,Body-Weight Trajectory
+BMGC_DS20075,BMG_DS077794,Gestational Weight Gain
+BMGC_DS20076,BMG_DS077812,Shwachman-Diamond syndrome
+BMGC_DS20077,BMG_DS077813,Ototoxicity
+BMGC_DS20078,BMG_DS077814,Pulmonary Arterial Hypertension
+BMGC_DS20079,BMG_DS077832,Chemotherapy-Related Cognitive Impairment
+BMGC_DS20080,BMG_DS077833,Hyperthermia
+BMGC_DS20081,BMG_DS077834,"Mesothelioma, Malignant"
+BMGC_DS20082,BMG_DS077835,Anosmia
+BMGC_DS20083,BMG_DS077836,Rhinorrhea
+BMGC_DS20084,BMG_DS077876,"Melanoma, Cutaneous Malignant"
+BMGC_DS20085,BMG_DS077890,Uveal Melanoma
+BMGC_DS20086,BMG_DS077899,Achondroplasia
+BMGC_DS20087,BMG_DS077900,Acid-Base Imbalance
+BMGC_DS20088,BMG_DS077901,Acidosis
+BMGC_DS20089,BMG_DS077902,infantile mercury poisoning
+BMGC_DS20090,BMG_DS077904,Acute-Phase Reaction
+BMGC_DS20091,BMG_DS077905,Adenocarcinoma
+BMGC_DS20092,BMG_DS077909,Adenoma
+BMGC_DS20093,BMG_DS077912,"Adenoma, Acidophil"
+BMGC_DS20094,BMG_DS077913,Tissue Adhesions
+BMGC_DS20095,BMG_DS077914,Adrenal Cortex Neoplasms
+BMGC_DS20096,BMG_DS077915,Adrenal Insufficiency
+BMGC_DS20097,BMG_DS077916,Adrenal Gland Neoplasms
+BMGC_DS20098,BMG_DS077917,"Adrenal Hyperplasia, Congenital"
+BMGC_DS20099,BMG_DS077921,Ageusia
+BMGC_DS20100,BMG_DS077925,Albuminuria
+BMGC_DS20101,BMG_DS077927,Alcoholic Intoxication
+BMGC_DS20102,BMG_DS077928,Alcoholism
+BMGC_DS20103,BMG_DS077929,"Alkalosis, Respiratory"
+BMGC_DS20104,BMG_DS077930,"Alveolitis, Extrinsic Allergic"
+BMGC_DS20105,BMG_DS077931,ameloblastoma
+BMGC_DS20106,BMG_DS077932,Amelogenesis Imperfecta
+BMGC_DS20107,BMG_DS077933,Amenorrhea
+BMGC_DS20108,BMG_DS077934,Amnesia
+BMGC_DS20109,BMG_DS077935,"Amnesia, Retrograde"
+BMGC_DS20110,BMG_DS077938,Anaphylaxis
+BMGC_DS20111,BMG_DS077939,Anaplasia
+BMGC_DS20112,BMG_DS077940,"Anemia, Dyserythropoietic, Congenital"
+BMGC_DS20113,BMG_DS077941,"Anemia, Hypochromic"
+BMGC_DS20114,BMG_DS077942,"Anemia, Refractory"
+BMGC_DS20115,BMG_DS077943,"Anemia, Refractory, with Excess of Blasts"
+BMGC_DS20116,BMG_DS077944,"Anemia, Sideroblastic"
+BMGC_DS20117,BMG_DS077945,anencephaly
+BMGC_DS20118,BMG_DS077946,Aneuploidy
+BMGC_DS20119,BMG_DS077947,Aneurysm
+BMGC_DS20120,BMG_DS077948,Aortic Dissection
+BMGC_DS20121,BMG_DS077949,Angina Pectoris
+BMGC_DS20122,BMG_DS077950,Angiokeratoma
+BMGC_DS20123,BMG_DS077951,Angioedema
+BMGC_DS20124,BMG_DS077952,aniseikonia
+BMGC_DS20125,BMG_DS077953,Ankylosis
+BMGC_DS20126,BMG_DS077954,Anodontia
+BMGC_DS20127,BMG_DS077956,Anophthalmos
+BMGC_DS20128,BMG_DS077957,Hypoxia
+BMGC_DS20129,BMG_DS077958,Anthrax
+BMGC_DS20130,BMG_DS077959,Anus Neoplasms
+BMGC_DS20131,BMG_DS077960,"Anus, Imperforate"
+BMGC_DS20132,BMG_DS077961,Aortic Coarctation
+BMGC_DS20133,BMG_DS077962,"Aortic Stenosis, Subvalvular"
+BMGC_DS20134,BMG_DS077963,Aortic Valve Stenosis
+BMGC_DS20135,BMG_DS077964,Aortopulmonary Septal Defect
+BMGC_DS20136,BMG_DS077969,Aphonia
+BMGC_DS20137,BMG_DS077970,Apnea
+BMGC_DS20138,BMG_DS077974,argyria
+BMGC_DS20139,BMG_DS077976,Arnold-Chiari Malformation
+BMGC_DS20140,BMG_DS077977,"Arrhythmia, Sinus"
+BMGC_DS20141,BMG_DS077980,obsolete rare arteriovenous malformation
+BMGC_DS20142,BMG_DS077981,Arteritis
+BMGC_DS20143,BMG_DS077982,"Arthritis, Experimental"
+BMGC_DS20144,BMG_DS077983,arthrogryposis syndrome
+BMGC_DS20145,BMG_DS077986,Asphyxia
+BMGC_DS20146,BMG_DS077987,Asthenia
+BMGC_DS20147,BMG_DS077989,Astrocytoma
+BMGC_DS20148,BMG_DS077991,Atrial Flutter
+BMGC_DS20149,BMG_DS077992,Atrophy
+BMGC_DS20150,BMG_DS077993,Auditory Perceptual Disorders
+BMGC_DS20151,BMG_DS077997,Bacteriuria
+BMGC_DS20152,BMG_DS077999,Basal Cell Nevus Syndrome
+BMGC_DS20153,BMG_DS078000,psychiatric disorder
+BMGC_DS20154,BMG_DS078002,Bile Duct Neoplasms
+BMGC_DS20155,BMG_DS078003,Biliary Atresia
+BMGC_DS20156,BMG_DS078005,Biliary Tract Neoplasms
+BMGC_DS20157,BMG_DS078007,Birth Weight
+BMGC_DS20158,BMG_DS078010,Urinary Bladder Calculi
+BMGC_DS20159,BMG_DS078012,Urinary Bladder Neck Obstruction
+BMGC_DS20160,BMG_DS078013,Urinary Bladder Neoplasms
+BMGC_DS20161,BMG_DS078014,Blast Crisis
+BMGC_DS20162,BMG_DS078016,Blister
+BMGC_DS20163,BMG_DS078019,Body Weight
+BMGC_DS20164,BMG_DS078020,Body Weight Changes
+BMGC_DS20165,BMG_DS078021,Bone Neoplasms
+BMGC_DS20166,BMG_DS078022,bone resorption disease
+BMGC_DS20167,BMG_DS078023,Bowen's Disease
+BMGC_DS20168,BMG_DS078024,Bradycardia
+BMGC_DS20169,BMG_DS078026,Brain Death
+BMGC_DS20170,BMG_DS078027,Brain Edema
+BMGC_DS20171,BMG_DS078028,brain injury
+BMGC_DS20172,BMG_DS078029,Brain Neoplasms
+BMGC_DS20173,BMG_DS078031,Breast Neoplasms
+BMGC_DS20174,BMG_DS078035,Bronchial Neoplasms
+BMGC_DS20175,BMG_DS078039,Bruxism
+BMGC_DS20176,BMG_DS078040,Bulimia
+BMGC_DS20177,BMG_DS078041,Burkitt Lymphoma
+BMGC_DS20178,BMG_DS078043,burn
+BMGC_DS20179,BMG_DS078044,"Burns, Chemical"
+BMGC_DS20180,BMG_DS078047,Cachexia
+BMGC_DS20181,BMG_DS078049,cadmium poisoning
+BMGC_DS20182,BMG_DS078050,Calcinosis
+BMGC_DS20183,BMG_DS078051,Calculi
+BMGC_DS20184,BMG_DS078054,cutaneous candidiasis
+BMGC_DS20185,BMG_DS078055,"Candidiasis, Oral"
+BMGC_DS20186,BMG_DS078056,Carbon Monoxide Poisoning
+BMGC_DS20187,BMG_DS078057,Carbon Tetrachloride Poisoning
+BMGC_DS20188,BMG_DS078059,Carcinoid Tumor
+BMGC_DS20189,BMG_DS078060,Carcinoma
+BMGC_DS20190,BMG_DS078061,Carcinoma in Situ
+BMGC_DS20191,BMG_DS078062,"Carcinoma 256, Walker"
+BMGC_DS20192,BMG_DS078063,"Carcinoma, Basal Cell"
+BMGC_DS20193,BMG_DS078065,"Adenocarcinoma, Bronchiolo-Alveolar"
+BMGC_DS20194,BMG_DS078066,"Carcinoma, Bronchogenic"
+BMGC_DS20195,BMG_DS078068,"Carcinoma, Intraductal, Noninfiltrating"
+BMGC_DS20196,BMG_DS078069,"Carcinoma, Ehrlich Tumor"
+BMGC_DS20197,BMG_DS078071,"Adenocarcinoma, Mucinous"
+BMGC_DS20198,BMG_DS078072,"Carcinoma, Non-Small-Cell Lung"
+BMGC_DS20199,BMG_DS078073,"Carcinoma, Papillary"
+BMGC_DS20200,BMG_DS078074,"Carcinoma, Renal Cell"
+BMGC_DS20201,BMG_DS078076,"Carcinoma, Squamous Cell"
+BMGC_DS20202,BMG_DS078077,"Carcinoma, Transitional Cell"
+BMGC_DS20203,BMG_DS078078,Carcinosarcoma
+BMGC_DS20204,BMG_DS078079,"Cardiac Output, Low"
+BMGC_DS20205,BMG_DS078080,"Cardiomyopathy, Restrictive"
+BMGC_DS20206,BMG_DS078082,Catalepsy
+BMGC_DS20207,BMG_DS078083,Cecal Neoplasms
+BMGC_DS20208,BMG_DS078084,"Cell Transformation, Neoplastic"
+BMGC_DS20209,BMG_DS078087,Central Nervous System Diseases
+BMGC_DS20210,BMG_DS078089,"Hypoxia, Brain"
+BMGC_DS20211,BMG_DS078090,Intracranial Arteriovenous Malformations
+BMGC_DS20212,BMG_DS078091,Cerebral Hemorrhage
+BMGC_DS20213,BMG_DS078093,Uterine Cervical Dysplasia
+BMGC_DS20214,BMG_DS078095,Uterine Cervical Neoplasms
+BMGC_DS20215,BMG_DS078098,acquired hyperprolactinemia
+BMGC_DS20216,BMG_DS078100,developmental disability
+BMGC_DS20217,BMG_DS078102,Choanal Atresia
+BMGC_DS20218,BMG_DS078103,"Adenoma, Bile Duct"
+BMGC_DS20219,BMG_DS078104,Chondroblastoma
+BMGC_DS20220,BMG_DS078105,Chondroma
+BMGC_DS20221,BMG_DS078106,Chondrosarcoma
+BMGC_DS20222,BMG_DS078107,Chordoma
+BMGC_DS20223,BMG_DS078112,Choroid Hemorrhage
+BMGC_DS20224,BMG_DS078113,Chromosome Aberrations
+BMGC_DS20225,BMG_DS078114,Chromosome Deletion
+BMGC_DS20226,BMG_DS078115,Chromosome Fragility
+BMGC_DS20227,BMG_DS078117,Cleft Lip
+BMGC_DS20228,BMG_DS078118,Cleft Palate
+BMGC_DS20229,BMG_DS078119,Clubfoot
+BMGC_DS20230,BMG_DS078124,Coloboma
+BMGC_DS20231,BMG_DS078125,Colonic Neoplasms
+BMGC_DS20232,BMG_DS078126,Colonic Polyps
+BMGC_DS20233,BMG_DS078128,Communication Disorders
+BMGC_DS20234,BMG_DS078129,Compartment Syndromes
+BMGC_DS20235,BMG_DS078130,Confusion
+BMGC_DS20236,BMG_DS078134,Consciousness Disorders
+BMGC_DS20237,BMG_DS078135,Constipation
+BMGC_DS20238,BMG_DS078136,"Constriction, Pathologic"
+BMGC_DS20239,BMG_DS078137,obsolete contracture
+BMGC_DS20240,BMG_DS078141,Corneal Opacity
+BMGC_DS20241,BMG_DS078142,Coronary Disease
+BMGC_DS20242,BMG_DS078143,Coronary Vessel Anomalies
+BMGC_DS20243,BMG_DS078144,Cough
+BMGC_DS20244,BMG_DS078147,Craniopharyngioma
+BMGC_DS20245,BMG_DS078148,Crigler-Najjar Syndrome
+BMGC_DS20246,BMG_DS078151,Cryptorchidism
+BMGC_DS20247,BMG_DS078152,Cyanosis
+BMGC_DS20248,BMG_DS078153,adenoid cystic carcinoma
+BMGC_DS20249,BMG_DS078155,Cystadenoma
+BMGC_DS20250,BMG_DS078156,Phyllodes Tumor
+BMGC_DS20251,BMG_DS078157,Cysts
+BMGC_DS20252,BMG_DS078158,"Hearing Loss, Sudden"
+BMGC_DS20253,BMG_DS078159,Death
+BMGC_DS20254,BMG_DS078160,"Death, Sudden"
+BMGC_DS20255,BMG_DS078162,Pressure Ulcer
+BMGC_DS20256,BMG_DS078163,Delirium
+BMGC_DS20257,BMG_DS078164,Dementia
+BMGC_DS20258,BMG_DS078171,"Dermatitis, Exfoliative"
+BMGC_DS20259,BMG_DS078173,Dextrocardia
+BMGC_DS20260,BMG_DS078174,"Diabetes Mellitus, Experimental"
+BMGC_DS20261,BMG_DS078177,Diarrhea
+BMGC_DS20262,BMG_DS078178,"Diarrhea, Infantile"
+BMGC_DS20263,BMG_DS078179,Vipoma
+BMGC_DS20264,BMG_DS078181,Digestive System Abnormalities
+BMGC_DS20265,BMG_DS078182,Digestive System Neoplasms
+BMGC_DS20266,BMG_DS078183,"Dilatation, Pathologic"
+BMGC_DS20267,BMG_DS078185,"Disease Models, Animal"
+BMGC_DS20268,BMG_DS078186,Disease Susceptibility
+BMGC_DS20269,BMG_DS078189,Dizziness
+BMGC_DS20270,BMG_DS078191,Drug Hypersensitivity
+BMGC_DS20271,BMG_DS078192,"Ductus Arteriosus, Patent"
+BMGC_DS20272,BMG_DS078194,"Dwarfism, Pituitary"
+BMGC_DS20273,BMG_DS078195,Dysarthria
+BMGC_DS20274,BMG_DS078197,Dysgeusia
+BMGC_DS20275,BMG_DS078198,Dyslexia
+BMGC_DS20276,BMG_DS078201,Dyspepsia
+BMGC_DS20277,BMG_DS078203,Dyspnea
+BMGC_DS20278,BMG_DS078204,Dystocia
+BMGC_DS20279,BMG_DS078205,Dystonia
+BMGC_DS20280,BMG_DS078207,auditory system cancer
+BMGC_DS20281,BMG_DS078209,Ebstein Anomaly
+BMGC_DS20282,BMG_DS078212,Ectopia Lentis
+BMGC_DS20283,BMG_DS078213,Ectromelia
+BMGC_DS20284,BMG_DS078214,Edema
+BMGC_DS20285,BMG_DS078215,"Edema, Cardiac"
+BMGC_DS20286,BMG_DS078217,Emaciation
+BMGC_DS20287,BMG_DS078218,Embolism
+BMGC_DS20288,BMG_DS078222,Emphysema
+BMGC_DS20289,BMG_DS078224,Encephalocele
+BMGC_DS20290,BMG_DS078227,Endocardial Cushion Defects
+BMGC_DS20291,BMG_DS078229,Endomyocardial Fibrosis
+BMGC_DS20292,BMG_DS078231,Ependymoma
+BMGC_DS20293,BMG_DS078233,Epidermodysplasia Verruciformis
+BMGC_DS20294,BMG_DS078234,Epidermolysis Bullosa
+BMGC_DS20295,BMG_DS078236,Epistaxis
+BMGC_DS20296,BMG_DS078242,"Leukemia, Erythroblastic, Acute"
+BMGC_DS20297,BMG_DS078243,Esophageal Atresia
+BMGC_DS20298,BMG_DS078247,Esophageal Neoplasms
+BMGC_DS20299,BMG_DS078249,Exanthema
+BMGC_DS20300,BMG_DS078250,"Exostoses, Multiple Hereditary"
+BMGC_DS20301,BMG_DS078251,Extravasation of Diagnostic and Therapeutic Materials
+BMGC_DS20302,BMG_DS078252,Eye Abnormalities
+BMGC_DS20303,BMG_DS078253,Eye Burns
+BMGC_DS20304,BMG_DS078254,visual impairment and progressive phthisis bulbi
+BMGC_DS20305,BMG_DS078256,Eye Hemorrhage
+BMGC_DS20306,BMG_DS078257,Eye Injuries
+BMGC_DS20307,BMG_DS078258,Eye Manifestations
+BMGC_DS20308,BMG_DS078259,Eye Neoplasms
+BMGC_DS20309,BMG_DS078261,Facial Asymmetry
+BMGC_DS20310,BMG_DS078262,Facial Injuries
+BMGC_DS20311,BMG_DS078264,Facial Pain
+BMGC_DS20312,BMG_DS078265,Factor V Deficiency
+BMGC_DS20313,BMG_DS078266,Factor XI Deficiency
+BMGC_DS20314,BMG_DS078267,Factor XIII Deficiency
+BMGC_DS20315,BMG_DS078269,Fasciculation
+BMGC_DS20316,BMG_DS078271,Fatigue
+BMGC_DS20317,BMG_DS078274,Feminization
+BMGC_DS20318,BMG_DS078275,Femoral Fractures
+BMGC_DS20319,BMG_DS078278,Fetal Death
+BMGC_DS20320,BMG_DS078279,Fetal Distress
+BMGC_DS20321,BMG_DS078280,Fetal Growth Retardation
+BMGC_DS20322,BMG_DS078281,Fetal Macrosomia
+BMGC_DS20323,BMG_DS078284,Fever
+BMGC_DS20324,BMG_DS078286,fibroma
+BMGC_DS20325,BMG_DS078288,Fibrosarcoma
+BMGC_DS20326,BMG_DS078289,Finger Injuries
+BMGC_DS20327,BMG_DS078290,Fistula
+BMGC_DS20328,BMG_DS078292,Flatfoot
+BMGC_DS20329,BMG_DS078294,Fluoride Poisoning
+BMGC_DS20330,BMG_DS078295,Flushing
+BMGC_DS20331,BMG_DS078297,Follicular Cyst
+BMGC_DS20332,BMG_DS078298,Foodborne Diseases
+BMGC_DS20333,BMG_DS078301,"Foot Deformities, Congenital"
+BMGC_DS20334,BMG_DS078305,Foreign-Body Reaction
+BMGC_DS20335,BMG_DS078307,"Fractures, Closed"
+BMGC_DS20336,BMG_DS078312,Fructose Intolerance
+BMGC_DS20337,BMG_DS078316,Gallbladder Neoplasms
+BMGC_DS20338,BMG_DS078318,Gas Poisoning
+BMGC_DS20339,BMG_DS078319,Gastric Fistula
+BMGC_DS20340,BMG_DS078320,Gastroesophageal Reflux
+BMGC_DS20341,BMG_DS078321,Gastrointestinal Neoplasms
+BMGC_DS20342,BMG_DS078322,"Genital Neoplasms, Female"
+BMGC_DS20343,BMG_DS078325,Castleman Disease
+BMGC_DS20344,BMG_DS078326,Tourette Syndrome
+BMGC_DS20345,BMG_DS078327,Gingival Hemorrhage
+BMGC_DS20346,BMG_DS078328,Gingival Hyperplasia
+BMGC_DS20347,BMG_DS078331,Gingival Recession
+BMGC_DS20348,BMG_DS078332,Glioblastoma
+BMGC_DS20349,BMG_DS078333,Glioma
+BMGC_DS20350,BMG_DS078334,Gliosis
+BMGC_DS20351,BMG_DS078337,Glossalgia
+BMGC_DS20352,BMG_DS078338,Glucagonoma
+BMGC_DS20353,BMG_DS078339,Glucosephosphate Dehydrogenase Deficiency
+BMGC_DS20354,BMG_DS078340,Glycosuria
+BMGC_DS20355,BMG_DS078341,"Glycosuria, Renal"
+BMGC_DS20356,BMG_DS078343,Gonadal Dysgenesis
+BMGC_DS20357,BMG_DS078344,"Graft Occlusion, Vascular"
+BMGC_DS20358,BMG_DS078345,Granuloma
+BMGC_DS20359,BMG_DS078346,"Granuloma, Plasma Cell"
+BMGC_DS20360,BMG_DS078347,Granulosa Cell Tumor
+BMGC_DS20361,BMG_DS078348,Growth Disorders
+BMGC_DS20362,BMG_DS078349,Halitosis
+BMGC_DS20363,BMG_DS078350,Hallucinations
+BMGC_DS20364,BMG_DS078352,Hamartoma
+BMGC_DS20365,BMG_DS078355,"Hand Deformities, Congenital"
+BMGC_DS20366,BMG_DS078357,"Rhinitis, Allergic, Seasonal"
+BMGC_DS20367,BMG_DS078358,Head and Neck Neoplasms
+BMGC_DS20368,BMG_DS078359,Craniocerebral Trauma
+BMGC_DS20369,BMG_DS078360,Headache
+BMGC_DS20370,BMG_DS078361,"Hearing Loss, Conductive"
+BMGC_DS20371,BMG_DS078363,"Hearing Loss, Noise-Induced"
+BMGC_DS20372,BMG_DS078364,"Hearing Loss, Sensorineural"
+BMGC_DS20373,BMG_DS078365,"Heart Defects, Congenital"
+BMGC_DS20374,BMG_DS078366,Cardiomegaly
+BMGC_DS20375,BMG_DS078367,Heart Injuries
+BMGC_DS20376,BMG_DS078369,Heart Septal Defects
+BMGC_DS20377,BMG_DS078370,"Heart Septal Defects, Atrial"
+BMGC_DS20378,BMG_DS078371,"Heart Septal Defects, Ventricular"
+BMGC_DS20379,BMG_DS078372,Heart Valve Diseases
+BMGC_DS20380,BMG_DS078373,Heartburn
+BMGC_DS20381,BMG_DS078376,Hemangioendothelioma
+BMGC_DS20382,BMG_DS078377,Hemangioma
+BMGC_DS20383,BMG_DS078379,Hemangiopericytoma
+BMGC_DS20384,BMG_DS078380,Hemangiosarcoma
+BMGC_DS20385,BMG_DS078382,Hematemesis
+BMGC_DS20386,BMG_DS078384,Hematoma
+BMGC_DS20387,BMG_DS078385,"Hematoma, Epidural, Cranial"
+BMGC_DS20388,BMG_DS078386,"Hematoma, Subdural"
+BMGC_DS20389,BMG_DS078389,Hemoglobinuria
+BMGC_DS20390,BMG_DS078390,Hemolysis
+BMGC_DS20391,BMG_DS078391,Hemoperitoneum
+BMGC_DS20392,BMG_DS078393,Hemorrhage
+BMGC_DS20393,BMG_DS078395,Postpartum Hemorrhage
+BMGC_DS20394,BMG_DS078396,Hemothorax
+BMGC_DS20395,BMG_DS078397,"Carcinoma, Hepatocellular"
+BMGC_DS20396,BMG_DS078398,Hepatomegaly
+BMGC_DS20397,BMG_DS078400,"Hernia, Diaphragmatic"
+BMGC_DS20398,BMG_DS078404,obsolete umbilical hernia
+BMGC_DS20399,BMG_DS078406,Heroin Dependence
+BMGC_DS20400,BMG_DS078407,Herpes Simplex
+BMGC_DS20401,BMG_DS078409,Hiccup
+BMGC_DS20402,BMG_DS078414,hip fracture
+BMGC_DS20403,BMG_DS078415,von Hippel-Lindau Disease
+BMGC_DS20404,BMG_DS078416,HIV Seropositivity
+BMGC_DS20405,BMG_DS078418,Hodgkins lymphoma
+BMGC_DS20406,BMG_DS078420,Hydatidiform Mole
+BMGC_DS20407,BMG_DS078421,Polyhydramnios
+BMGC_DS20408,BMG_DS078422,Hydranencephaly
+BMGC_DS20409,BMG_DS078424,Testicular Hydrocele
+BMGC_DS20410,BMG_DS078427,Hyperalgesia
+BMGC_DS20411,BMG_DS078428,Hypercapnia
+BMGC_DS20412,BMG_DS078430,Hyperesthesia
+BMGC_DS20413,BMG_DS078431,Hyperhidrosis
+BMGC_DS20414,BMG_DS078432,Hyperkalemia
+BMGC_DS20415,BMG_DS078433,Hyperphagia
+BMGC_DS20416,BMG_DS078434,Hyperplasia
+BMGC_DS20417,BMG_DS078435,Hypersensitivity
+BMGC_DS20418,BMG_DS078436,"Hypersensitivity, Delayed"
+BMGC_DS20419,BMG_DS078437,"Hypersensitivity, Immediate"
+BMGC_DS20420,BMG_DS078438,obsolete hypertelorism
+BMGC_DS20421,BMG_DS078439,Hypertension
+BMGC_DS20422,BMG_DS078440,"Hypertension, Pulmonary"
+BMGC_DS20423,BMG_DS078441,"Hypertension, Renal"
+BMGC_DS20424,BMG_DS078442,Hypertrophy
+BMGC_DS20425,BMG_DS078443,Hyperventilation
+BMGC_DS20426,BMG_DS078444,Hypesthesia
+BMGC_DS20427,BMG_DS078445,Hyphema
+BMGC_DS20428,BMG_DS078446,Hypokalemia
+BMGC_DS20429,BMG_DS078448,Hypospadias
+BMGC_DS20430,BMG_DS078449,Hypotension
+BMGC_DS20431,BMG_DS078451,Hypothermia
+BMGC_DS20432,BMG_DS078452,Hypoventilation
+BMGC_DS20433,BMG_DS078456,Immunoblastic Lymphadenopathy
+BMGC_DS20434,BMG_DS078457,Immunoproliferative Disorders
+BMGC_DS20435,BMG_DS078459,Erectile Dysfunction
+BMGC_DS20436,BMG_DS078460,Incontinentia Pigmenti
+BMGC_DS20437,BMG_DS078462,"Infant, Newborn, Diseases"
+BMGC_DS20438,BMG_DS078463,Infarction
+BMGC_DS20439,BMG_DS078464,Infections
+BMGC_DS20440,BMG_DS078465,Infertility
+BMGC_DS20441,BMG_DS078466,"Infertility, Male"
+BMGC_DS20442,BMG_DS078467,Inflammation
+BMGC_DS20443,BMG_DS078468,Insect Bites and Stings
+BMGC_DS20444,BMG_DS078469,Insulin Resistance
+BMGC_DS20445,BMG_DS078470,Insulinoma
+BMGC_DS20446,BMG_DS078471,Intestinal Neoplasms
+BMGC_DS20447,BMG_DS078472,Intestinal Polyps
+BMGC_DS20448,BMG_DS078473,Intraoperative Complications
+BMGC_DS20449,BMG_DS078475,Ischemia
+BMGC_DS20450,BMG_DS078476,"Adenoma, Islet Cell"
+BMGC_DS20451,BMG_DS078477,Jaw Abnormalities
+BMGC_DS20452,BMG_DS078482,Joint Instability
+BMGC_DS20453,BMG_DS078484,Kearns-Sayre Syndrome
+BMGC_DS20454,BMG_DS078485,Keloid
+BMGC_DS20455,BMG_DS078486,herpes simplex virus keratitis
+BMGC_DS20456,BMG_DS078487,Keratoacanthoma
+BMGC_DS20457,BMG_DS078488,Kidney Calculi
+BMGC_DS20458,BMG_DS078489,Kidney Neoplasms
+BMGC_DS20459,BMG_DS078493,Kyphosis
+BMGC_DS20460,BMG_DS078495,"Obstetric Labor, Premature"
+BMGC_DS20461,BMG_DS078496,Labyrinth Diseases
+BMGC_DS20462,BMG_DS078497,Lacrimal Duct Obstruction
+BMGC_DS20463,BMG_DS078498,"lameness, non-human animal"
+BMGC_DS20464,BMG_DS078499,Language Disorders
+BMGC_DS20465,BMG_DS078500,Laryngeal Edema
+BMGC_DS20466,BMG_DS078501,Laryngeal Neoplasms
+BMGC_DS20467,BMG_DS078503,lead poisoning
+BMGC_DS20468,BMG_DS078504,Learning Disabilities
+BMGC_DS20469,BMG_DS078507,Legg-Calve-Perthes Disease
+BMGC_DS20470,BMG_DS078508,Leiomyoma
+BMGC_DS20471,BMG_DS078509,Leiomyosarcoma
+BMGC_DS20472,BMG_DS078510,"Leishmaniasis, Mucocutaneous"
+BMGC_DS20473,BMG_DS078511,Leukemia
+BMGC_DS20474,BMG_DS078512,Leukemia L1210
+BMGC_DS20475,BMG_DS078515,"Leukemia, Experimental"
+BMGC_DS20476,BMG_DS078516,"Leukemia, Hairy Cell"
+BMGC_DS20477,BMG_DS078517,"Leukemia, Lymphoid"
+BMGC_DS20478,BMG_DS078519,"Leukemia, Megakaryoblastic, Acute"
+BMGC_DS20479,BMG_DS078520,"Leukemia, Monocytic, Acute"
+BMGC_DS20480,BMG_DS078521,"Leukemia, Myeloid"
+BMGC_DS20481,BMG_DS078523,"Leukemia, Radiation-Induced"
+BMGC_DS20482,BMG_DS078525,"Leukoplakia, Oral"
+BMGC_DS20483,BMG_DS078528,Leydig Cell Tumor
+BMGC_DS20484,BMG_DS078529,Linitis Plastica
+BMGC_DS20485,BMG_DS078531,Lipoma
+BMGC_DS20486,BMG_DS078532,Liposarcoma
+BMGC_DS20487,BMG_DS078533,"Liver Cirrhosis, Experimental"
+BMGC_DS20488,BMG_DS078534,Liver Diseases
+BMGC_DS20489,BMG_DS078535,Liver Neoplasms
+BMGC_DS20490,BMG_DS078536,"Liver Neoplasms, Experimental"
+BMGC_DS20491,BMG_DS078538,Long QT Syndrome
+BMGC_DS20492,BMG_DS078539,Lordosis
+BMGC_DS20493,BMG_DS078545,Lung Diseases
+BMGC_DS20494,BMG_DS078546,Lung Neoplasms
+BMGC_DS20495,BMG_DS078547,"Lupus Erythematosus, Discoid"
+BMGC_DS20496,BMG_DS078551,Lymphatic Metastasis
+BMGC_DS20497,BMG_DS078552,Lymphoma
+BMGC_DS20498,BMG_DS078553,follicular lymphoma
+BMGC_DS20499,BMG_DS078554,"Lymphoma, Non-Hodgkin"
+BMGC_DS20500,BMG_DS078556,Lymphoproliferative Disorders
+BMGC_DS20501,BMG_DS078557,obsolete macroglobulinemia
+BMGC_DS20502,BMG_DS078558,Macrostomia
+BMGC_DS20503,BMG_DS078559,Macular Degeneration
+BMGC_DS20504,BMG_DS078562,Malignant Hyperthermia
+BMGC_DS20505,BMG_DS078563,Malocclusion
+BMGC_DS20506,BMG_DS078567,"Mammary Neoplasms, Experimental"
+BMGC_DS20507,BMG_DS078570,Mandibular Neoplasms
+BMGC_DS20508,BMG_DS078572,Mastocytosis
+BMGC_DS20509,BMG_DS078574,Maxillary Neoplasms
+BMGC_DS20510,BMG_DS078575,Maxillary Sinus Neoplasms
+BMGC_DS20511,BMG_DS078578,Mediastinal Neoplasms
+BMGC_DS20512,BMG_DS078579,Medulloblastoma
+BMGC_DS20513,BMG_DS078580,Megacolon
+BMGC_DS20514,BMG_DS078582,Melanoma
+BMGC_DS20515,BMG_DS078583,"Melanoma, Experimental"
+BMGC_DS20516,BMG_DS078584,Melena
+BMGC_DS20517,BMG_DS078585,Memory Disorders
+BMGC_DS20518,BMG_DS078587,Meningioma
+BMGC_DS20519,BMG_DS078588,Meningism
+BMGC_DS20520,BMG_DS078590,Meningocele
+BMGC_DS20521,BMG_DS078591,Meningomyelocele
+BMGC_DS20522,BMG_DS078592,Menorrhagia
+BMGC_DS20523,BMG_DS078593,Intellectual Disability
+BMGC_DS20524,BMG_DS078594,mercury poisoning
+BMGC_DS20525,BMG_DS078599,Mesothelioma
+BMGC_DS20526,BMG_DS078600,Metaplasia
+BMGC_DS20527,BMG_DS078601,Metrorrhagia
+BMGC_DS20528,BMG_DS078602,Micrognathism
+BMGC_DS20529,BMG_DS078603,Microphthalmos
+BMGC_DS20530,BMG_DS078606,Monoclonal Gammopathy of Undetermined Significance
+BMGC_DS20531,BMG_DS078607,Monosomy
+BMGC_DS20532,BMG_DS078608,"Abnormalities, Severe Teratoid"
+BMGC_DS20533,BMG_DS078610,Morphine Dependence
+BMGC_DS20534,BMG_DS078611,"Fluorosis, Dental"
+BMGC_DS20535,BMG_DS078612,Mouth Abnormalities
+BMGC_DS20536,BMG_DS078613,Mouth Breathing
+BMGC_DS20537,BMG_DS078614,Mouth Neoplasms
+BMGC_DS20538,BMG_DS078616,Mucocele
+BMGC_DS20539,BMG_DS078617,Multiple Myeloma
+BMGC_DS20540,BMG_DS078619,Muscle Cramp
+BMGC_DS20541,BMG_DS078620,Muscle Hypertonia
+BMGC_DS20542,BMG_DS078621,Muscle Rigidity
+BMGC_DS20543,BMG_DS078622,Muscle Spasticity
+BMGC_DS20544,BMG_DS078623,Muscular Atrophy
+BMGC_DS20545,BMG_DS078624,Musculoskeletal Abnormalities
+BMGC_DS20546,BMG_DS078626,Mycosis Fungoides
+BMGC_DS20547,BMG_DS078627,Myelodysplastic Syndromes
+BMGC_DS20548,BMG_DS078628,Myeloproliferative Disorders
+BMGC_DS20549,BMG_DS078630,obsolete hereditary myoglobinuria
+BMGC_DS20550,BMG_DS078631,Myoma
+BMGC_DS20551,BMG_DS078633,Myotonia
+BMGC_DS20552,BMG_DS078637,Opioid-Related Disorders
+BMGC_DS20553,BMG_DS078638,Nasal Polyps
+BMGC_DS20554,BMG_DS078639,Nasopharyngeal Neoplasms
+BMGC_DS20555,BMG_DS078640,Nausea
+BMGC_DS20556,BMG_DS078641,Necrosis
+BMGC_DS20557,BMG_DS078643,Nematode Infections
+BMGC_DS20558,BMG_DS078644,"Neoplastic Cells, Circulating"
+BMGC_DS20559,BMG_DS078645,Neoplasm Invasiveness
+BMGC_DS20560,BMG_DS078646,Neoplasm Metastasis
+BMGC_DS20561,BMG_DS078647,"Neoplasm Recurrence, Local"
+BMGC_DS20562,BMG_DS078648,"Neoplasm Regression, Spontaneous"
+BMGC_DS20563,BMG_DS078649,Neoplasm Seeding
+BMGC_DS20564,BMG_DS078650,Neoplasms
+BMGC_DS20565,BMG_DS078652,organ system cancer
+BMGC_DS20566,BMG_DS078654,obsolete germ cell and embryonal cancer
+BMGC_DS20567,BMG_DS078655,"Neoplasms, Experimental"
+BMGC_DS20568,BMG_DS078656,"Neoplasms, Glandular and Epithelial"
+BMGC_DS20569,BMG_DS078657,"Neoplasms, Hormone-Dependent"
+BMGC_DS20570,BMG_DS078658,multiple endocrine neoplasia
+BMGC_DS20571,BMG_DS078662,"Neoplasms, Radiation-Induced"
+BMGC_DS20572,BMG_DS078665,Neoplastic Processes
+BMGC_DS20573,BMG_DS078667,"Neovascularization, Pathologic"
+BMGC_DS20574,BMG_DS078668,Nerve Degeneration
+BMGC_DS20575,BMG_DS078669,Nervous System Malformations
+BMGC_DS20576,BMG_DS078670,Nervous System Diseases
+BMGC_DS20577,BMG_DS078672,Neurilemmoma
+BMGC_DS20578,BMG_DS078673,"Neuritis, Autoimmune, Experimental"
+BMGC_DS20579,BMG_DS078674,Neuroblastoma
+BMGC_DS20580,BMG_DS078675,Neurofibroma
+BMGC_DS20581,BMG_DS078676,Neurofibromatosis 1
+BMGC_DS20582,BMG_DS078677,Neurologic Manifestations
+BMGC_DS20583,BMG_DS078680,Nevus
+BMGC_DS20584,BMG_DS078682,"Nevus, Pigmented"
+BMGC_DS20585,BMG_DS078684,"Nose Deformities, Acquired"
+BMGC_DS20586,BMG_DS078685,Nose Neoplasms
+BMGC_DS20587,BMG_DS078686,"Obesity, Morbid"
+BMGC_DS20588,BMG_DS078689,Oligodendroglioma
+BMGC_DS20589,BMG_DS078690,Oligomenorrhea
+BMGC_DS20590,BMG_DS078696,Oropharyngeal Neoplasms
+BMGC_DS20591,BMG_DS078697,"Ossification, Heterotopic"
+BMGC_DS20592,BMG_DS078698,Osteolysis
+BMGC_DS20593,BMG_DS078705,Ovarian Neoplasms
+BMGC_DS20594,BMG_DS078707,cutaneous Paget disease
+BMGC_DS20595,BMG_DS078708,Pain
+BMGC_DS20596,BMG_DS078709,"Pain, Intractable"
+BMGC_DS20597,BMG_DS078713,Exocrine Pancreatic Insufficiency
+BMGC_DS20598,BMG_DS078714,Pancreatic Neoplasms
+BMGC_DS20599,BMG_DS078715,Papilloma
+BMGC_DS20600,BMG_DS078716,Paraganglioma
+BMGC_DS20601,BMG_DS078717,"Paraganglioma, Extra-Adrenal"
+BMGC_DS20602,BMG_DS078718,Paralysis
+BMGC_DS20603,BMG_DS078720,Paranasal Sinus Diseases
+BMGC_DS20604,BMG_DS078722,Paraneoplastic Syndromes
+BMGC_DS20605,BMG_DS078723,Parathyroid Neoplasms
+BMGC_DS20606,BMG_DS078728,"Pemphigoid, Bullous"
+BMGC_DS20607,BMG_DS078729,Penile Neoplasms
+BMGC_DS20608,BMG_DS078730,active peptic ulcer disease
+BMGC_DS20609,BMG_DS078731,Perceptual Disorders
+BMGC_DS20610,BMG_DS078735,Peritoneal Neoplasms
+BMGC_DS20611,BMG_DS078736,Pharyngeal Neoplasms
+BMGC_DS20612,BMG_DS078737,Phencyclidine Abuse
+BMGC_DS20613,BMG_DS078738,pheochromocytoma
+BMGC_DS20614,BMG_DS078739,Philadelphia Chromosome
+BMGC_DS20615,BMG_DS078741,Pica
+BMGC_DS20616,BMG_DS078742,Pierre Robin Syndrome
+BMGC_DS20617,BMG_DS078743,Pilonidal Sinus
+BMGC_DS20618,BMG_DS078745,Pituitary Neoplasms
+BMGC_DS20619,BMG_DS078746,Placenta Accreta
+BMGC_DS20620,BMG_DS078747,Placenta Diseases
+BMGC_DS20621,BMG_DS078749,Plant Poisoning
+BMGC_DS20622,BMG_DS078750,Plasmacytoma
+BMGC_DS20623,BMG_DS078752,Pleural Effusion
+BMGC_DS20624,BMG_DS078753,Pleural Neoplasms
+BMGC_DS20625,BMG_DS078754,"Pneumonia, Pneumococcal"
+BMGC_DS20626,BMG_DS078755,"Pneumonia, Pneumocystis"
+BMGC_DS20627,BMG_DS078756,Rothmund-Thomson Syndrome
+BMGC_DS20628,BMG_DS078757,poisoning
+BMGC_DS20629,BMG_DS078758,Polycythemia Vera
+BMGC_DS20630,BMG_DS078759,Polyploidy
+BMGC_DS20631,BMG_DS078760,Polyps
+BMGC_DS20632,BMG_DS078761,Polyuria
+BMGC_DS20633,BMG_DS078765,Postoperative Complications
+BMGC_DS20634,BMG_DS078766,Pre-Eclampsia
+BMGC_DS20635,BMG_DS078767,Precancerous Conditions
+BMGC_DS20636,BMG_DS078768,Prediabetic State
+BMGC_DS20637,BMG_DS078769,Pregnancy Complications
+BMGC_DS20638,BMG_DS078772,"Pregnancy, Ectopic"
+BMGC_DS20639,BMG_DS078773,"Pregnancy, Prolonged"
+BMGC_DS20640,BMG_DS078776,Prenatal Exposure Delayed Effects
+BMGC_DS20641,BMG_DS078780,Prostatic Neoplasms
+BMGC_DS20642,BMG_DS078781,Proteinuria
+BMGC_DS20643,BMG_DS078782,Pruritus
+BMGC_DS20644,BMG_DS078787,Psychomotor Agitation
+BMGC_DS20645,BMG_DS078788,Psychomotor Disorders
+BMGC_DS20646,BMG_DS078789,Psychophysiologic Disorders
+BMGC_DS20647,BMG_DS078791,"Psychoses, Substance-Induced"
+BMGC_DS20648,BMG_DS078792,Pterygium
+BMGC_DS20649,BMG_DS078793,"Puberty, Delayed"
+BMGC_DS20650,BMG_DS078794,Pulmonary Edema
+BMGC_DS20651,BMG_DS078795,Pulmonary Heart Disease
+BMGC_DS20652,BMG_DS078798,Pulmonary Veno-Occlusive Disease
+BMGC_DS20653,BMG_DS078802,"Radiation Injuries, Experimental"
+BMGC_DS20654,BMG_DS078806,Hyperacusis
+BMGC_DS20655,BMG_DS078807,anal fistula
+BMGC_DS20656,BMG_DS078808,Rectal Neoplasms
+BMGC_DS20657,BMG_DS078810,Recurrence
+BMGC_DS20658,BMG_DS078811,"Reflex, Abnormal"
+BMGC_DS20659,BMG_DS078813,Respiratory Hypersensitivity
+BMGC_DS20660,BMG_DS078814,Respiratory Paralysis
+BMGC_DS20661,BMG_DS078815,Respiratory Sounds
+BMGC_DS20662,BMG_DS078817,Retinal Degeneration
+BMGC_DS20663,BMG_DS078818,Retinal Hemorrhage
+BMGC_DS20664,BMG_DS078819,Retinoblastoma
+BMGC_DS20665,BMG_DS078820,Retrograde Degeneration
+BMGC_DS20666,BMG_DS078821,Retroperitoneal Fibrosis
+BMGC_DS20667,BMG_DS078822,Retroperitoneal Neoplasms
+BMGC_DS20668,BMG_DS078824,obsolete rhabdomyolysis
+BMGC_DS20669,BMG_DS078825,Rhabdomyoma
+BMGC_DS20670,BMG_DS078826,Rhabdomyosarcoma
+BMGC_DS20671,BMG_DS078832,Rupture
+BMGC_DS20672,BMG_DS078833,"Rupture, Spontaneous"
+BMGC_DS20673,BMG_DS078836,Salivary Gland Neoplasms
+BMGC_DS20674,BMG_DS078837,Salmonella Food Poisoning
+BMGC_DS20675,BMG_DS078838,Salmonella Infections
+BMGC_DS20676,BMG_DS078839,Sarcoma
+BMGC_DS20677,BMG_DS078842,"Sarcoma, Ewing"
+BMGC_DS20678,BMG_DS078843,"Sarcoma, Experimental"
+BMGC_DS20679,BMG_DS078844,"Sarcoma, Kaposi"
+BMGC_DS20680,BMG_DS078846,Osteosarcoma
+BMGC_DS20681,BMG_DS078850,Sclerosis
+BMGC_DS20682,BMG_DS078851,Scoliosis
+BMGC_DS20683,BMG_DS078852,Scotoma
+BMGC_DS20684,BMG_DS078853,Sebaceous Gland Neoplasms
+BMGC_DS20685,BMG_DS078855,Self Mutilation
+BMGC_DS20686,BMG_DS078858,"Sexual Dysfunction, Physiological"
+BMGC_DS20687,BMG_DS078859,Sezary Syndrome
+BMGC_DS20688,BMG_DS078860,Shock
+BMGC_DS20689,BMG_DS078861,"Shock, Cardiogenic"
+BMGC_DS20690,BMG_DS078862,"Shock, Hemorrhagic"
+BMGC_DS20691,BMG_DS078864,"Shock, Traumatic"
+BMGC_DS20692,BMG_DS078866,Sigmoid Neoplasms
+BMGC_DS20693,BMG_DS078867,Signs and Symptoms
+BMGC_DS20694,BMG_DS078868,"Signs and Symptoms, Digestive"
+BMGC_DS20695,BMG_DS078869,"Signs and Symptoms, Respiratory"
+BMGC_DS20696,BMG_DS078870,Situs Inversus
+BMGC_DS20697,BMG_DS078871,Skin Abnormalities
+BMGC_DS20698,BMG_DS078872,Skin Diseases
+BMGC_DS20699,BMG_DS078873,Skin Manifestations
+BMGC_DS20700,BMG_DS078874,Skin Neoplasms
+BMGC_DS20701,BMG_DS078878,Sneezing
+BMGC_DS20702,BMG_DS078880,Soft Tissue Neoplasms
+BMGC_DS20703,BMG_DS078882,Spasm
+BMGC_DS20704,BMG_DS078883,"Spherocytosis, Hereditary"
+BMGC_DS20705,BMG_DS078884,spinal cord injury
+BMGC_DS20706,BMG_DS078886,Spinal Curvatures
+BMGC_DS20707,BMG_DS078890,Splenic Neoplasms
+BMGC_DS20708,BMG_DS078892,Splenomegaly
+BMGC_DS20709,BMG_DS078893,"Spondylitis, Ankylosing"
+BMGC_DS20710,BMG_DS078895,Starvation
+BMGC_DS20711,BMG_DS078897,Stomach Neoplasms
+BMGC_DS20712,BMG_DS078898,Stomach Ulcer
+BMGC_DS20713,BMG_DS078900,Subcutaneous Emphysema
+BMGC_DS20714,BMG_DS078903,Substance Withdrawal Syndrome
+BMGC_DS20715,BMG_DS078904,obsolete sudden infant death syndrome
+BMGC_DS20716,BMG_DS078905,Sunburn
+BMGC_DS20717,BMG_DS078907,Suppuration
+BMGC_DS20718,BMG_DS078909,Surgical Wound Infection
+BMGC_DS20719,BMG_DS078911,Sweat Gland Neoplasms
+BMGC_DS20720,BMG_DS078912,"Pathological Conditions, Signs and Symptoms"
+BMGC_DS20721,BMG_DS078913,Syndactyly
+BMGC_DS20722,BMG_DS078916,"Sarcoma, Synovial"
+BMGC_DS20723,BMG_DS078918,Tachycardia
+BMGC_DS20724,BMG_DS078919,"Tachycardia, Supraventricular"
+BMGC_DS20725,BMG_DS078920,Telangiectasis
+BMGC_DS20726,BMG_DS078921,Tendon Injuries
+BMGC_DS20727,BMG_DS078923,Testicular Neoplasms
+BMGC_DS20728,BMG_DS078924,Tetralogy of Fallot
+BMGC_DS20729,BMG_DS078928,Thoracic Neoplasms
+BMGC_DS20730,BMG_DS078929,Thromboembolism
+BMGC_DS20731,BMG_DS078930,thrombosis
+BMGC_DS20732,BMG_DS078931,Thymoma
+BMGC_DS20733,BMG_DS078932,Thymus Neoplasms
+BMGC_DS20734,BMG_DS078934,Thyroid Neoplasms
+BMGC_DS20735,BMG_DS078935,"Thyroiditis, Autoimmune"
+BMGC_DS20736,BMG_DS078937,tibia fracture
+BMGC_DS20737,BMG_DS078938,Tobacco Use Disorder
+BMGC_DS20738,BMG_DS078939,Tongue Neoplasms
+BMGC_DS20739,BMG_DS078943,Tooth Abnormalities
+BMGC_DS20740,BMG_DS078944,Tooth Abrasion
+BMGC_DS20741,BMG_DS078945,Tooth Discoloration
+BMGC_DS20742,BMG_DS078953,Toothache
+BMGC_DS20743,BMG_DS078955,Torticollis
+BMGC_DS20744,BMG_DS078956,Toxemia
+BMGC_DS20745,BMG_DS078958,Tracheoesophageal Fistula
+BMGC_DS20746,BMG_DS078959,"Translocation, Genetic"
+BMGC_DS20747,BMG_DS078960,Transposition of Great Vessels
+BMGC_DS20748,BMG_DS078962,Tremor
+BMGC_DS20749,BMG_DS078963,trichotillomania
+BMGC_DS20750,BMG_DS078964,Trichuriasis
+BMGC_DS20751,BMG_DS078966,Trisomy
+BMGC_DS20752,BMG_DS078968,"Truncus Arteriosus, Persistent"
+BMGC_DS20753,BMG_DS078969,Tuberous Sclerosis
+BMGC_DS20754,BMG_DS078971,"Twins, Conjoined"
+BMGC_DS20755,BMG_DS078972,Ulcer
+BMGC_DS20756,BMG_DS078974,Unconsciousness
+BMGC_DS20757,BMG_DS078975,Ureteral Diseases
+BMGC_DS20758,BMG_DS078976,Ureteral Neoplasms
+BMGC_DS20759,BMG_DS078977,Ureteral Obstruction
+BMGC_DS20760,BMG_DS078980,Urinary Calculi
+BMGC_DS20761,BMG_DS078982,Urinary Incontinence
+BMGC_DS20762,BMG_DS078983,urinary tract infection
+BMGC_DS20763,BMG_DS078984,Urogenital Abnormalities
+BMGC_DS20764,BMG_DS078985,obsolete urogenital neoplasm
+BMGC_DS20765,BMG_DS078986,Urologic Neoplasms
+BMGC_DS20766,BMG_DS078988,Uterine Hemorrhage
+BMGC_DS20767,BMG_DS078990,Uterine Neoplasms
+BMGC_DS20768,BMG_DS078992,Uterine Rupture
+BMGC_DS20769,BMG_DS078994,"Uveitis, Anterior"
+BMGC_DS20770,BMG_DS078996,Vaginal Neoplasms
+BMGC_DS20771,BMG_DS078997,Varicose Veins
+BMGC_DS20772,BMG_DS079000,Virilism
+BMGC_DS20773,BMG_DS079002,Vomiting
+BMGC_DS20774,BMG_DS079004,Vulvar Neoplasms
+BMGC_DS20775,BMG_DS079005,Wallerian Degeneration
+BMGC_DS20776,BMG_DS079006,Water-Electrolyte Imbalance
+BMGC_DS20777,BMG_DS079007,Granulomatosis with Polyangiitis
+BMGC_DS20778,BMG_DS079010,injury
+BMGC_DS20779,BMG_DS079013,"Wounds, Penetrating"
+BMGC_DS20780,BMG_DS079017,Xeroderma Pigmentosum
+BMGC_DS20781,BMG_DS079024,Supratentorial Neoplasms
+BMGC_DS20782,BMG_DS079026,Prolactinoma
+BMGC_DS20783,BMG_DS079027,Colorectal Neoplasms
+BMGC_DS20784,BMG_DS079029,"Osteoarthritis, Hip"
+BMGC_DS20785,BMG_DS079030,Smoke Inhalation Injury
+BMGC_DS20786,BMG_DS079031,"Carcinoma, Merkel Cell"
+BMGC_DS20787,BMG_DS079032,Churg-Strauss Syndrome
+BMGC_DS20788,BMG_DS079033,Gastrinoma
+BMGC_DS20789,BMG_DS079034,ischemia reperfusion injury
+BMGC_DS20790,BMG_DS079035,Myocardial Reperfusion Injury
+BMGC_DS20791,BMG_DS079036,Weight Gain
+BMGC_DS20792,BMG_DS079037,Weight Loss
+BMGC_DS20793,BMG_DS079040,"Leukemia, Lymphocytic, Chronic, B-Cell"
+BMGC_DS20794,BMG_DS079041,Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
+BMGC_DS20795,BMG_DS079043,"Leukemia, T-Cell"
+BMGC_DS20796,BMG_DS079044,"Leukemia-Lymphoma, Adult T-Cell"
+BMGC_DS20797,BMG_DS079045,"Leukemia, Prolymphocytic, T-Cell"
+BMGC_DS20798,BMG_DS079047,"Leukemia, Myelogenous, Chronic, BCR-ABL Positive"
+BMGC_DS20799,BMG_DS079048,"Leukemia, Myeloid, Accelerated Phase"
+BMGC_DS20800,BMG_DS079051,"Leukemia, Myeloid, Acute"
+BMGC_DS20801,BMG_DS079054,"Leukemia, Promyelocytic, Acute"
+BMGC_DS20802,BMG_DS079055,"Leukemia, Myelomonocytic, Chronic"
+BMGC_DS20803,BMG_DS079056,"Leukemia, Myelomonocytic, Acute"
+BMGC_DS20804,BMG_DS079057,Choledochal Cyst
+BMGC_DS20805,BMG_DS079058,Histiocytosis
+BMGC_DS20806,BMG_DS079060,"Histiocytosis, Sinus"
+BMGC_DS20807,BMG_DS079061,Respiratory System Abnormalities
+BMGC_DS20808,BMG_DS079063,mycotoxicosis
+BMGC_DS20809,BMG_DS079064,"mammary neoplasms, animal"
+BMGC_DS20810,BMG_DS079067,"Granuloma, Foreign-Body"
+BMGC_DS20811,BMG_DS079068,Abdominal Pain
+BMGC_DS20812,BMG_DS079070,Aniridia
+BMGC_DS20813,BMG_DS079071,Retinal Dysplasia
+BMGC_DS20814,BMG_DS079074,"Substance Abuse, Intravenous"
+BMGC_DS20815,BMG_DS079076,Osteochondroma
+BMGC_DS20816,BMG_DS079079,Anisocoria
+BMGC_DS20817,BMG_DS079080,Miosis
+BMGC_DS20818,BMG_DS079081,Mydriasis
+BMGC_DS20819,BMG_DS079082,Urinary Retention
+BMGC_DS20820,BMG_DS079083,"Blood Loss, Surgical"
+BMGC_DS20821,BMG_DS079085,Oligohydramnios
+BMGC_DS20822,BMG_DS079086,oculocutaneous albinism
+BMGC_DS20823,BMG_DS079087,ocular albinism 1
+BMGC_DS20824,BMG_DS079088,Spinal Dysraphism
+BMGC_DS20825,BMG_DS079089,spina bifida occulta
+BMGC_DS20826,BMG_DS079090,Spina Bifida Cystica
+BMGC_DS20827,BMG_DS079091,Holoprosencephaly
+BMGC_DS20828,BMG_DS079092,Oral Fistula
+BMGC_DS20829,BMG_DS079093,Respiratory Tract Fistula
+BMGC_DS20830,BMG_DS079097,Tooth Loss
+BMGC_DS20831,BMG_DS079098,"Lymphoma, B-Cell"
+BMGC_DS20832,BMG_DS079099,"Lymphoma, T-Cell"
+BMGC_DS20833,BMG_DS079101,diffuse large B-cell lymphoma
+BMGC_DS20834,BMG_DS079102,primary cutaneous T-cell non-Hodgkin lymphoma
+BMGC_DS20835,BMG_DS079103,"Lymphoma, T-Cell, Peripheral"
+BMGC_DS20836,BMG_DS079105,Bacteremia
+BMGC_DS20837,BMG_DS079106,"Lymphoma, AIDS-Related"
+BMGC_DS20838,BMG_DS079108,"Pemphigus, Benign Familial"
+BMGC_DS20839,BMG_DS079110,Neurofibromatosis 2
+BMGC_DS20840,BMG_DS079111,"Cardiac Output, High"
+BMGC_DS20841,BMG_DS079112,Central Nervous System Neoplasms
+BMGC_DS20842,BMG_DS079114,"Purpura, Thrombocytopenic, Idiopathic"
+BMGC_DS20843,BMG_DS079116,seasonal affective disorder
+BMGC_DS20844,BMG_DS079122,"Neoplasms, Second Primary"
+BMGC_DS20845,BMG_DS079125,"Plasma Cell Granuloma, Pulmonary"
+BMGC_DS20846,BMG_DS079126,"Death, Sudden, Cardiac"
+BMGC_DS20847,BMG_DS079129,herpes simplex virus keratitis
+BMGC_DS20848,BMG_DS079130,Hypocapnia
+BMGC_DS20849,BMG_DS079131,Endometrial Neoplasms
+BMGC_DS20850,BMG_DS079133,IgA Deficiency
+BMGC_DS20851,BMG_DS079137,"Ophthalmoplegia, Chronic Progressive External"
+BMGC_DS20852,BMG_DS079138,Neurofibromatoses
+BMGC_DS20853,BMG_DS079139,Leukemic Infiltration
+BMGC_DS20854,BMG_DS079142,Acneiform Eruptions
+BMGC_DS20855,BMG_DS079143,"Keratosis, Seborrheic"
+BMGC_DS20856,BMG_DS079144,Hyperpigmentation
+BMGC_DS20857,BMG_DS079145,Hypopigmentation
+BMGC_DS20858,BMG_DS079147,Iliac Aneurysm
+BMGC_DS20859,BMG_DS079148,"Aortic Aneurysm, Abdominal"
+BMGC_DS20860,BMG_DS079149,"Aortic Aneurysm, Thoracic"
+BMGC_DS20861,BMG_DS079153,Neuroectodermal Tumors
+BMGC_DS20862,BMG_DS079155,Polydactyly
+BMGC_DS20863,BMG_DS079158,"Lymphoma, Large-Cell, Anaplastic"
+BMGC_DS20864,BMG_DS079159,Lymphomatoid Papulosis
+BMGC_DS20865,BMG_DS079164,"Limb Deformities, Congenital"
+BMGC_DS20866,BMG_DS079168,Glucose Intolerance
+BMGC_DS20867,BMG_DS079171,Lymphangioleiomyomatosis
+BMGC_DS20868,BMG_DS079176,Hepatoblastoma
+BMGC_DS20869,BMG_DS079179,"Mixed Tumor, Mullerian"
+BMGC_DS20870,BMG_DS079187,"Liposarcoma, Myxoid"
+BMGC_DS20871,BMG_DS079190,"Chondrosarcoma, Mesenchymal"
+BMGC_DS20872,BMG_DS079191,Giant Cell Tumor of Bone
+BMGC_DS20873,BMG_DS079192,"Neoplasms, Bone Tissue"
+BMGC_DS20874,BMG_DS079197,"Neoplasms, Fibrous Tissue"
+BMGC_DS20875,BMG_DS079198,"Histiocytoma, Benign Fibrous"
+BMGC_DS20876,BMG_DS079200,"Fibromatosis, Abdominal"
+BMGC_DS20877,BMG_DS079201,Desmoid Tumors
+BMGC_DS20878,BMG_DS079205,Fibroadenoma
+BMGC_DS20879,BMG_DS079206,"Sarcoma, Clear Cell"
+BMGC_DS20880,BMG_DS079209,"Leiomyoma, Epithelioid"
+BMGC_DS20881,BMG_DS079211,"Rhabdomyosarcoma, Alveolar"
+BMGC_DS20882,BMG_DS079212,"Rhabdomyosarcoma, Embryonal"
+BMGC_DS20883,BMG_DS079213,"Sarcoma, Alveolar Soft Part"
+BMGC_DS20884,BMG_DS079214,Smooth Muscle Tumor
+BMGC_DS20885,BMG_DS079215,"Carcinoma, Embryonal"
+BMGC_DS20886,BMG_DS079218,Seminoma
+BMGC_DS20887,BMG_DS079219,Endodermal Sinus Tumor
+BMGC_DS20888,BMG_DS079220,"Neuroectodermal Tumors, Primitive, Peripheral"
+BMGC_DS20889,BMG_DS079221,"Neuroectodermal Tumors, Primitive"
+BMGC_DS20890,BMG_DS079222,Teratocarcinoma
+BMGC_DS20891,BMG_DS079224,Adrenocortical Adenoma
+BMGC_DS20892,BMG_DS079225,"Adenoma, Liver Cell"
+BMGC_DS20893,BMG_DS079226,"Adenoma, Oxyphilic"
+BMGC_DS20894,BMG_DS079233,Adenomatous Polyps
+BMGC_DS20895,BMG_DS079235,"Adenocarcinoma, Clear Cell"
+BMGC_DS20896,BMG_DS079236,"Adenocarcinoma, Follicular"
+BMGC_DS20897,BMG_DS079240,Adrenocortical Carcinoma
+BMGC_DS20898,BMG_DS079241,"Carcinoma, Endometrioid"
+BMGC_DS20899,BMG_DS079242,"Carcinoma, Ductal, Breast"
+BMGC_DS20900,BMG_DS079244,"Carcinoma, Lobular"
+BMGC_DS20901,BMG_DS079245,"Carcinoma, Medullary"
+BMGC_DS20902,BMG_DS079246,"Carcinoma, Mucoepidermoid"
+BMGC_DS20903,BMG_DS079250,Cholangiocarcinoma
+BMGC_DS20904,BMG_DS079256,"Carcinoma, Large Cell"
+BMGC_DS20905,BMG_DS079257,"Carcinoma, Small Cell"
+BMGC_DS20906,BMG_DS079264,Pilomatrixoma
+BMGC_DS20907,BMG_DS079269,"Neoplasms, Mesothelial"
+BMGC_DS20908,BMG_DS079275,"Neoplasms, Squamous Cell"
+BMGC_DS20909,BMG_DS079282,Gliosarcoma
+BMGC_DS20910,BMG_DS079283,Nerve Sheath Neoplasms
+BMGC_DS20911,BMG_DS079284,"Neurofibroma, Plexiform"
+BMGC_DS20912,BMG_DS079285,Neurofibrosarcoma
+BMGC_DS20913,BMG_DS079288,"Hemangioendothelioma, Epithelioid"
+BMGC_DS20914,BMG_DS079290,Hemangioblastoma
+BMGC_DS20915,BMG_DS079291,Nevi and Melanomas
+BMGC_DS20916,BMG_DS079293,"Melanoma, Amelanotic"
+BMGC_DS20917,BMG_DS079297,"Nevus, Epithelioid and Spindle Cell"
+BMGC_DS20918,BMG_DS079299,Rhabdoid Tumor
+BMGC_DS20919,BMG_DS079300,Neuroendocrine Tumors
+BMGC_DS20920,BMG_DS079301,"Neoplasm, Residual"
+BMGC_DS20921,BMG_DS079302,Cardiovascular Abnormalities
+BMGC_DS20922,BMG_DS079305,marginal zone lymphoma
+BMGC_DS20923,BMG_DS079306,Disease Progression
+BMGC_DS20924,BMG_DS079308,Hypokinesia
+BMGC_DS20925,BMG_DS079309,"Ventricular Dysfunction, Left"
+BMGC_DS20926,BMG_DS079310,Hyperoxia
+BMGC_DS20927,BMG_DS079311,"Ventricular Dysfunction, Right"
+BMGC_DS20928,BMG_DS079312,"Breast Neoplasms, Male"
+BMGC_DS20929,BMG_DS079315,"Vitreoretinopathy, Proliferative"
+BMGC_DS20930,BMG_DS079317,Stomatognathic System Abnormalities
+BMGC_DS20931,BMG_DS079318,Tooth Injuries
+BMGC_DS20932,BMG_DS079319,Ventricular Dysfunction
+BMGC_DS20933,BMG_DS079320,Multiple Endocrine Neoplasia Type 1
+BMGC_DS20934,BMG_DS079321,tricuspid atresia
+BMGC_DS20935,BMG_DS079322,"Anemia, Iron-Deficiency"
+BMGC_DS20936,BMG_DS079323,Multiple Endocrine Neoplasia Type 2a
+BMGC_DS20937,BMG_DS079324,Multiple Endocrine Neoplasia Type 2b
+BMGC_DS20938,BMG_DS079325,"Carcinoma, Lewis Lung"
+BMGC_DS20939,BMG_DS079326,Ventricular Premature Complexes
+BMGC_DS20940,BMG_DS079327,Heat Stress Disorders
+BMGC_DS20941,BMG_DS079328,Heat Stroke
+BMGC_DS20942,BMG_DS079331,Muscle Weakness
+BMGC_DS20943,BMG_DS079333,Vascular Neoplasms
+BMGC_DS20944,BMG_DS079334,Bone Marrow Neoplasms
+BMGC_DS20945,BMG_DS079335,Prostatic Intraepithelial Neoplasia
+BMGC_DS20946,BMG_DS079337,Facies
+BMGC_DS20947,BMG_DS079338,Cafe-au-Lait Spots
+BMGC_DS20948,BMG_DS079339,Postoperative Hemorrhage
+BMGC_DS20949,BMG_DS079344,Pseudolymphoma
+BMGC_DS20950,BMG_DS079346,Hematologic Neoplasms
+BMGC_DS20951,BMG_DS079347,Port-Wine Stain
+BMGC_DS20952,BMG_DS079348,Chromosome Breakage
+BMGC_DS20953,BMG_DS079349,Craniofacial Abnormalities
+BMGC_DS20954,BMG_DS079351,Neck Pain
+BMGC_DS20955,BMG_DS079355,Multiple System Atrophy
+BMGC_DS20956,BMG_DS079356,Hot Flashes
+BMGC_DS20957,BMG_DS079357,Intracranial Hypertension
+BMGC_DS20958,BMG_DS079358,"Aging, Premature"
+BMGC_DS20959,BMG_DS079361,Maxillofacial Abnormalities
+BMGC_DS20960,BMG_DS079363,Neurobehavioral Manifestations
+BMGC_DS20961,BMG_DS079364,Substance-Related Disorders
+BMGC_DS20962,BMG_DS079365,Amphetamine-Related Disorders
+BMGC_DS20963,BMG_DS079366,Cocaine-Related Disorders
+BMGC_DS20964,BMG_DS079367,Genetic Predisposition to Disease
+BMGC_DS20965,BMG_DS079370,Neurogenic Inflammation
+BMGC_DS20966,BMG_DS079371,Acquired Hyperostosis Syndrome
+BMGC_DS20967,BMG_DS079373,Putaminal Hemorrhage
+BMGC_DS20968,BMG_DS079374,manganese poisoning
+BMGC_DS20969,BMG_DS079375,Ornithine Carbamoyltransferase Deficiency Disease
+BMGC_DS20970,BMG_DS079378,nervous system injury
+BMGC_DS20971,BMG_DS079380,"Intracranial Hemorrhage, Traumatic"
+BMGC_DS20972,BMG_DS079381,"Hematoma, Subdural, Acute"
+BMGC_DS20973,BMG_DS079382,"Hematoma, Subdural, Chronic"
+BMGC_DS20974,BMG_DS079383,"Brain Hemorrhage, Traumatic"
+BMGC_DS20975,BMG_DS079392,vascular brain injury
+BMGC_DS20976,BMG_DS079395,Optic Nerve Injuries
+BMGC_DS20977,BMG_DS079397,Serotonin Syndrome
+BMGC_DS20978,BMG_DS079399,Gait Ataxia
+BMGC_DS20979,BMG_DS079400,"Amnesia, Transient Global"
+BMGC_DS20980,BMG_DS079404,Postoperative Nausea and Vomiting
+BMGC_DS20981,BMG_DS079405,Choroidal Neovascularization
+BMGC_DS20982,BMG_DS079406,Ventricular Remodeling
+BMGC_DS20983,BMG_DS079407,toxic encephalopathy
+BMGC_DS20984,BMG_DS079408,"Heavy Metal Poisoning, Nervous System"
+BMGC_DS20985,BMG_DS079409,"Lead Poisoning, Nervous System"
+BMGC_DS20986,BMG_DS079410,"Papilloma, Choroid Plexus"
+BMGC_DS20987,BMG_DS079411,Brain Stem Neoplasms
+BMGC_DS20988,BMG_DS079413,obsolete intracranial hemorrhage
+BMGC_DS20989,BMG_DS079415,Tics
+BMGC_DS20990,BMG_DS079417,Paraparesis
+BMGC_DS20991,BMG_DS079418,"Paraparesis, Spastic"
+BMGC_DS20992,BMG_DS079420,Lithiasis
+BMGC_DS20993,BMG_DS079422,"Nystagmus, Congenital"
+BMGC_DS20994,BMG_DS079423,Olfactory Nerve Diseases
+BMGC_DS20995,BMG_DS079425,Hypokalemic Periodic Paralysis
+BMGC_DS20996,BMG_DS079426,Fetal Weight
+BMGC_DS20997,BMG_DS079429,Amaurosis Fugax
+BMGC_DS20998,BMG_DS079430,"Pathological Conditions, Anatomical"
+BMGC_DS20999,BMG_DS079432,"Hemangioma, Cavernous, Central Nervous System"
+BMGC_DS21000,BMG_DS079435,Photophobia
+BMGC_DS21001,BMG_DS079438,Neuromuscular Manifestations
+BMGC_DS21002,BMG_DS079439,Hypovolemia
+BMGC_DS21003,BMG_DS079440,Korsakoff Syndrome
+BMGC_DS21004,BMG_DS079442,Embryo Loss
+BMGC_DS21005,BMG_DS079444,obsolete wheat allergic disease
+BMGC_DS21006,BMG_DS079445,obsolete peanut allergic reaction
+BMGC_DS21007,BMG_DS079446,"Carcinoma, Pancreatic Ductal"
+BMGC_DS21008,BMG_DS079447,Flank Pain
+BMGC_DS21009,BMG_DS079448,"Aortic Stenosis, Supravalvular"
+BMGC_DS21010,BMG_DS079449,Hyperammonemia
+BMGC_DS21011,BMG_DS079451,Chills
+BMGC_DS21012,BMG_DS079452,chlamydia infectious disease
+BMGC_DS21013,BMG_DS079453,"Gonadal Dysgenesis, 46,XX"
+BMGC_DS21014,BMG_DS079458,"Anemia, Hypoplastic, Congenital"
+BMGC_DS21015,BMG_DS079460,Human papillomavirus infectious disease
+BMGC_DS21016,BMG_DS079463,obsolete gestational trophoblastic disease
+BMGC_DS21017,BMG_DS079465,Hearing Loss
+BMGC_DS21018,BMG_DS079466,"Mastocytosis, Systemic"
+BMGC_DS21019,BMG_DS079469,ciguatera fish poisoning
+BMGC_DS21020,BMG_DS079472,"Lower Extremity Deformities, Congenital"
+BMGC_DS21021,BMG_DS079473,"Upper Extremity Deformities, Congenital"
+BMGC_DS21022,BMG_DS079475,X-Linked Intellectual Disability
+BMGC_DS21023,BMG_DS079476,Coffin-Lowry Syndrome
+BMGC_DS21024,BMG_DS079477,Genomic Instability
+BMGC_DS21025,BMG_DS079478,Gallstones
+BMGC_DS21026,BMG_DS079479,Chromosomal Instability
+BMGC_DS21027,BMG_DS079482,Lymphatic Abnormalities
+BMGC_DS21028,BMG_DS079483,"Carcinoma, Ductal"
+BMGC_DS21029,BMG_DS079484,Reticulocytosis
+BMGC_DS21030,BMG_DS079489,"Hypertension, Pregnancy-Induced"
+BMGC_DS21031,BMG_DS079491,Gastrointestinal Stromal Tumors
+BMGC_DS21032,BMG_DS079492,"Hernia, Abdominal"
+BMGC_DS21033,BMG_DS079497,"Hematoma, Epidural, Spinal"
+BMGC_DS21034,BMG_DS079502,Premature Birth
+BMGC_DS21035,BMG_DS079503,Hepatic Insufficiency
+BMGC_DS21036,BMG_DS079504,"Micronuclei, Chromosome-Defective"
+BMGC_DS21037,BMG_DS079507,"Plagiocephaly, Nonsynostotic"
+BMGC_DS21038,BMG_DS079508,Prenatal Injuries
+BMGC_DS21039,BMG_DS079514,Growth Hormone-Secreting Pituitary Adenoma
+BMGC_DS21040,BMG_DS079515,ACTH-Secreting Pituitary Adenoma
+BMGC_DS21041,BMG_DS079516,Overweight
+BMGC_DS21042,BMG_DS079520,Stillbirth
+BMGC_DS21043,BMG_DS079521,bone fracture
+BMGC_DS21044,BMG_DS079524,Post-Dural Puncture Headache
+BMGC_DS21045,BMG_DS079525,Mobility Limitation
+BMGC_DS21046,BMG_DS079526,"Neuralgia, Postherpetic"
+BMGC_DS21047,BMG_DS079527,Hemospermia
+BMGC_DS21048,BMG_DS079530,"Histiocytoma, Malignant Fibrous"
+BMGC_DS21049,BMG_DS079532,mucositis
+BMGC_DS21050,BMG_DS079537,Dysuria
+BMGC_DS21051,BMG_DS079539,Nocturnal Enuresis
+BMGC_DS21052,BMG_DS079541,"Ectodermal Dysplasia 1, Anhidrotic"
+BMGC_DS21053,BMG_DS079542,"Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive"
+BMGC_DS21054,BMG_DS079545,Ichthyosis Bullosa of Siemens
+BMGC_DS21055,BMG_DS079546,Hypercalciuria
+BMGC_DS21056,BMG_DS079550,Stupor
+BMGC_DS21057,BMG_DS079551,Lethargy
+BMGC_DS21058,BMG_DS079552,Aspermia
+BMGC_DS21059,BMG_DS079554,Microsatellite Instability
+BMGC_DS21060,BMG_DS079555,"Leukemia, Large Granular Lymphocytic"
+BMGC_DS21061,BMG_DS079556,Vascular Malformations
+BMGC_DS21062,BMG_DS079559,Lissencephaly
+BMGC_DS21063,BMG_DS079562,Arachnodactyly
+BMGC_DS21064,BMG_DS079563,"Sinus Arrest, Cardiac"
+BMGC_DS21065,BMG_DS079565,Precursor Cell Lymphoblastic Leukemia-Lymphoma
+BMGC_DS21066,BMG_DS079566,Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
+BMGC_DS21067,BMG_DS079568,No-Reflow Phenomenon
+BMGC_DS21068,BMG_DS079569,X-linked spermatogenic failure 1
+BMGC_DS21069,BMG_DS079571,Solitary Fibrous Tumors
+BMGC_DS21070,BMG_DS079572,"Lymphoma, Extranodal NK-T-Cell"
+BMGC_DS21071,BMG_DS079574,"Leukemia, Myelomonocytic, Juvenile"
+BMGC_DS21072,BMG_DS079575,myelodysplastic/myeloproliferative disease
+BMGC_DS21073,BMG_DS079576,"Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative"
+BMGC_DS21074,BMG_DS079580,Hyperphosphatemia
+BMGC_DS21075,BMG_DS079585,histiocytic sarcoma
+BMGC_DS21076,BMG_DS079587,primary dysautonomia
+BMGC_DS21077,BMG_DS079588,Orthostatic Intolerance
+BMGC_DS21078,BMG_DS079590,Pallister-Hall Syndrome
+BMGC_DS21079,BMG_DS079591,Primary Graft Dysfunction
+BMGC_DS21080,BMG_DS079594,Delayed Emergence from Anesthesia
+BMGC_DS21081,BMG_DS079596,acute lung injury
+BMGC_DS21082,BMG_DS079600,"Keratosis, Actinic"
+BMGC_DS21083,BMG_DS079601,Muir-Torre Syndrome
+BMGC_DS21084,BMG_DS079602,Primary Myelofibrosis
+BMGC_DS21085,BMG_DS079603,Small Cell Lung Carcinoma
+BMGC_DS21086,BMG_DS079605,Lynch Syndrome II
+BMGC_DS21087,BMG_DS079614,"Obesity, Abdominal"
+BMGC_DS21088,BMG_DS079616,Airway Remodeling
+BMGC_DS21089,BMG_DS079622,Costello Syndrome
+BMGC_DS21090,BMG_DS079623,Silver-Russell Syndrome
+BMGC_DS21091,BMG_DS079624,Prolidase Deficiency
+BMGC_DS21092,BMG_DS079625,Monilethrix
+BMGC_DS21093,BMG_DS079626,Renal Colic
+BMGC_DS21094,BMG_DS079628,Barth Syndrome
+BMGC_DS21095,BMG_DS079634,Shellfish Poisoning
+BMGC_DS21096,BMG_DS079637,Wet Macular Degeneration
+BMGC_DS21097,BMG_DS079638,Frontotemporal Lobar Degeneration
+BMGC_DS21098,BMG_DS079640,Frontotemporal Dementia
+BMGC_DS21099,BMG_DS079642,Eosinophilic Esophagitis
+BMGC_DS21100,BMG_DS079644,Vascular System Injuries
+BMGC_DS21101,BMG_DS079656,Dent Disease
+BMGC_DS21102,BMG_DS079657,"Plaque, Amyloid"
+BMGC_DS21103,BMG_DS079658,"Plaque, Atherosclerotic"
+BMGC_DS21104,BMG_DS079659,tungiasis
+BMGC_DS21105,BMG_DS079661,Desmoplastic Small Round Cell Tumor
+BMGC_DS21106,BMG_DS079662,Neointima
+BMGC_DS21107,BMG_DS079664,Eye Pain
+BMGC_DS21108,BMG_DS079665,Retinal Telangiectasis
+BMGC_DS21109,BMG_DS079666,Sotos Syndrome
+BMGC_DS21110,BMG_DS079667,Smith-Magenis syndrome
+BMGC_DS21111,BMG_DS079668,Fraser syndrome
+BMGC_DS21112,BMG_DS079669,Enteropathy-Associated T-Cell Lymphoma
+BMGC_DS21113,BMG_DS079676,Megalencephaly
+BMGC_DS21114,BMG_DS079682,Aberrant Crypt Foci
+BMGC_DS21115,BMG_DS079683,Inflammatory Breast Neoplasms
+BMGC_DS21116,BMG_DS079686,Nociceptive Pain
+BMGC_DS21117,BMG_DS079688,Tachypnea
+BMGC_DS21118,BMG_DS079691,brachydactyly
+BMGC_DS21119,BMG_DS079692,Peripheral Nerve Injuries
+BMGC_DS21120,BMG_DS079693,Musculoskeletal Pain
+BMGC_DS21121,BMG_DS079694,Mastodynia
+BMGC_DS21122,BMG_DS079698,Anhedonia
+BMGC_DS21123,BMG_DS079700,Polydipsia
+BMGC_DS21124,BMG_DS079706,"Angina, Stable"
+BMGC_DS21125,BMG_DS079710,dyscalculia
+BMGC_DS21126,BMG_DS079717,Agenesis of Corpus Callosum
+BMGC_DS21127,BMG_DS079718,Vascular Calcification
+BMGC_DS21128,BMG_DS079719,Neoplasm Micrometastasis
+BMGC_DS21129,BMG_DS079733,Hereditary Breast and Ovarian Cancer Syndrome
+BMGC_DS21130,BMG_DS079736,Organophosphate Poisoning
+BMGC_DS21131,BMG_DS079739,steatocystoma multiplex
+BMGC_DS21132,BMG_DS079741,Lipoblastoma
+BMGC_DS21133,BMG_DS079743,Drug Overdose
+BMGC_DS21134,BMG_DS079745,Maternal Death
+BMGC_DS21135,BMG_DS079747,Retrognathia
+BMGC_DS21136,BMG_DS079749,Binge Drinking
+BMGC_DS21137,BMG_DS079752,Carcinogenesis
+BMGC_DS21138,BMG_DS079753,Myalgia
+BMGC_DS21139,BMG_DS079756,castration-resistant prostate carcinoma
+BMGC_DS21140,BMG_DS079760,obsolete chemically-induced disorder
+BMGC_DS21141,BMG_DS079761,Drug-Related Side Effects and Adverse Reactions
+BMGC_DS21142,BMG_DS079762,Triple Negative Breast Neoplasms
+BMGC_DS21143,BMG_DS079765,Teratogenesis
+BMGC_DS21144,BMG_DS079771,Corneal Injuries
+BMGC_DS21145,BMG_DS079778,"Hernias, Diaphragmatic, Congenital"
+BMGC_DS21146,BMG_DS079779,"Rhinitis, Allergic"
+BMGC_DS21147,BMG_DS079781,"Thyroid Carcinoma, Anaplastic"
+BMGC_DS21148,BMG_DS079784,polymicrogyria
+BMGC_DS21149,BMG_DS079785,Schizencephaly
+BMGC_DS21150,BMG_DS079787,Congenital Microtia
+BMGC_DS21151,BMG_DS079789,Perinatal Death
+BMGC_DS21152,BMG_DS079790,Infant Death
+BMGC_DS21153,BMG_DS079791,Cardiotoxicity
+BMGC_DS21154,BMG_DS079794,Vascular Remodeling
+BMGC_DS21155,BMG_DS079795,"Protein Aggregation, Pathological"
+BMGC_DS21156,BMG_DS079796,acrokeratosis verruciformis
+BMGC_DS21157,BMG_DS079797,adenylosuccinase lyase deficiency
+BMGC_DS21158,BMG_DS079798,pseudohypoparathyroidism type 1A
+BMGC_DS21159,BMG_DS079799,alcohol dependence
+BMGC_DS21160,BMG_DS079800,Finnish type amyloidosis
+BMGC_DS21161,BMG_DS079801,CST3-related cerebral amyloid angiopathy
+BMGC_DS21162,BMG_DS079802,familial visceral amyloidosis
+BMGC_DS21163,BMG_DS079803,intracranial berry aneurysm 1
+BMGC_DS21164,BMG_DS079804,hereditary angioedema type I
+BMGC_DS21165,BMG_DS079805,isolated anhidrosis with normal sweat glands
+BMGC_DS21166,BMG_DS079806,aniridia 1
+BMGC_DS21167,BMG_DS079807,ankylosing spondylitis 1
+BMGC_DS21168,BMG_DS079808,nonsyndromic aplasia cutis congenita
+BMGC_DS21169,BMG_DS079809,Stickler syndrome 1
+BMGC_DS21170,BMG_DS079810,spermatogenic failure 2
+BMGC_DS21171,BMG_DS079811,spastic ataxia 1
+BMGC_DS21172,BMG_DS079812,spastic ataxia 7
+BMGC_DS21173,BMG_DS079813,atelosteogenesis
+BMGC_DS21174,BMG_DS079814,androgenic alopecia
+BMGC_DS21175,BMG_DS079815,nevoid basal cell carcinoma syndrome 1
+BMGC_DS21176,BMG_DS079816,primary biliary cholangitis 1
+BMGC_DS21177,BMG_DS079817,aortic valve disease 1
+BMGC_DS21178,BMG_DS079818,brachydactyly type B1
+BMGC_DS21179,BMG_DS079819,brachydactyly type D
+BMGC_DS21180,BMG_DS079820,brachydactyly type E1
+BMGC_DS21181,BMG_DS079821,branchiooculofacial syndrome
+BMGC_DS21182,BMG_DS079822,branchiootorenal syndrome 1
+BMGC_DS21183,BMG_DS079823,progressive familial heart block type IA
+BMGC_DS21184,BMG_DS079824,small intestine carcinoid neuroendocrine tumor
+BMGC_DS21185,BMG_DS079825,progressive familial heart block
+BMGC_DS21186,BMG_DS079826,cardiofaciocutaneous syndrome 1
+BMGC_DS21187,BMG_DS079827,hypertrophic cardiomyopathy 2
+BMGC_DS21188,BMG_DS079828,hypertrophic cardiomyopathy 3
+BMGC_DS21189,BMG_DS079829,hypertrophic cardiomyopathy 4
+BMGC_DS21190,BMG_DS079830,dilated cardiomyopathy 1A
+BMGC_DS21191,BMG_DS079831,restrictive cardiomyopathy 1
+BMGC_DS21192,BMG_DS079832,cerebral cavernous malformation 1
+BMGC_DS21193,BMG_DS079833,leukocyte adhesion deficiency 1
+BMGC_DS21194,BMG_DS079834,spinocerebellar ataxia type 31
+BMGC_DS21195,BMG_DS079835,ITM2B-related cerebral amyloid angiopathy 2
+BMGC_DS21196,BMG_DS079836,spinocerebellar ataxia type 29
+BMGC_DS21197,BMG_DS079837,Sotos syndrome 1
+BMGC_DS21198,BMG_DS079838,Klippel-Feil syndrome 1
+BMGC_DS21199,BMG_DS079839,familial chylomicronemia due to inhibition of lipoprotein lipase activity
+BMGC_DS21200,BMG_DS079840,cone-rod dystrophy 2
+BMGC_DS21201,BMG_DS079841,familial febrile seizures 1
+BMGC_DS21202,BMG_DS079842,granular corneal dystrophy 1
+BMGC_DS21203,BMG_DS079843,Cornelia de Lange syndrome 1
+BMGC_DS21204,BMG_DS079844,warfarin resistance
+BMGC_DS21205,BMG_DS079845,autosomal dominant craniodiaphyseal dysplasia
+BMGC_DS21206,BMG_DS079846,craniosynostosis 1
+BMGC_DS21207,BMG_DS079847,isolated elevated serum creatine phosphokinase levels
+BMGC_DS21208,BMG_DS079848,Beare-Stevenson cutis gyrata syndrome
+BMGC_DS21209,BMG_DS079849,autosomal dominant congenital deafness with onychodystrophy
+BMGC_DS21210,BMG_DS079850,nephrogenic diabetes insipidus type 2
+BMGC_DS21211,BMG_DS079851,maturity-onset diabetes of the young type 1
+BMGC_DS21212,BMG_DS079852,maturity-onset diabetes of the young type 2
+BMGC_DS21213,BMG_DS079853,Kenny-Caffey syndrome type 2
+BMGC_DS21214,BMG_DS079854,Ehlers-Danlos syndrome classic type 2
+BMGC_DS21215,BMG_DS079855,vascular type Ehlers-Danlos syndrome
+BMGC_DS21216,BMG_DS079856,Ehlers-Danlos syndrome spondylodysplastic type 1
+BMGC_DS21217,BMG_DS079857,autosomal dominant dystrophic epidermolysis bullosa
+BMGC_DS21218,BMG_DS079858,epidermolysis bullosa simplex localized type
+BMGC_DS21219,BMG_DS079859,pretibial dystrophic epidermolysis bullosa
+BMGC_DS21220,BMG_DS079860,spinocerebellar ataxia type 34
+BMGC_DS21221,BMG_DS079861,Cockayne syndrome B
+BMGC_DS21222,BMG_DS079862,autosomal hemophilia A
+BMGC_DS21223,BMG_DS079863,congenital fibrosis of the extraocular muscles 1
+BMGC_DS21224,BMG_DS079864,adermatoglyphia
+BMGC_DS21225,BMG_DS079865,frontonasal dysplasia 1
+BMGC_DS21226,BMG_DS079866,Gamstorp-Wohlfart syndrome
+BMGC_DS21227,BMG_DS079867,extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue
+BMGC_DS21228,BMG_DS079868,iridogoniodysgenesis syndrome
+BMGC_DS21229,BMG_DS079869,maturity-onset diabetes of the young type 5
+BMGC_DS21230,BMG_DS079870,hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
+BMGC_DS21231,BMG_DS079871,multinodular goiter
+BMGC_DS21232,BMG_DS079872,Heinz body anemia
+BMGC_DS21233,BMG_DS079873,benign familial hematuria
+BMGC_DS21234,BMG_DS079874,familial hepatic adenoma
+BMGC_DS21235,BMG_DS079875,developmental dysplasia of the hip 1
+BMGC_DS21236,BMG_DS079876,spondyloepiphyseal dysplasia with congenital joint dislocations
+BMGC_DS21237,BMG_DS079877,epidermolytic palmoplantar keratoderma 1
+BMGC_DS21238,BMG_DS079878,familial apolipoprotein A5 deficiency
+BMGC_DS21239,BMG_DS079879,nonpapillary renal cell carcinoma
+BMGC_DS21240,BMG_DS079880,familial progressive hyperpigmentation with or without hypopigmentation
+BMGC_DS21241,BMG_DS079881,Teebi hypertelorism syndrome 1
+BMGC_DS21242,BMG_DS079882,dystransthyretinemic hyperthyroxinemia
+BMGC_DS21243,BMG_DS079883,Charcot-Marie-Tooth disease type 3
+BMGC_DS21244,BMG_DS079884,adult hypophosphatasia
+BMGC_DS21245,BMG_DS079885,hypotrichosis 2
+BMGC_DS21246,BMG_DS079886,hypotrichosis 4
+BMGC_DS21247,BMG_DS079887,solitary median maxillary central incisor
+BMGC_DS21248,BMG_DS079888,punctate palmoplantar keratoderma type I
+BMGC_DS21249,BMG_DS079889,Bart-Pumphrey syndrome
+BMGC_DS21250,BMG_DS079890,lacrimoauriculodentodigital syndrome 1
+BMGC_DS21251,BMG_DS079891,Noonan syndrome with multiple lentigines 1
+BMGC_DS21252,BMG_DS079892,nonsyndromic congenital nail disorder 3
+BMGC_DS21253,BMG_DS079893,Li-Fraumeni syndrome 1
+BMGC_DS21254,BMG_DS079894,hereditary lymphedema IA
+BMGC_DS21255,BMG_DS079895,age related macular degeneration 2
+BMGC_DS21256,BMG_DS079896,Treacher Collins syndrome 1
+BMGC_DS21257,BMG_DS079897,Jansen's metaphyseal chondrodysplasia
+BMGC_DS21258,BMG_DS079898,Schmid metaphyseal chondrodysplasia
+BMGC_DS21259,BMG_DS079899,autosomal dominant progressive external ophthalmoplegia 1
+BMGC_DS21260,BMG_DS079900,autosomal dominant distal hereditary motor neuronopathy 7
+BMGC_DS21261,BMG_DS079901,spinal muscular atrophy with lower extremity predominant 1
+BMGC_DS21262,BMG_DS079902,facioscapulohumeral muscular dystrophy 2
+BMGC_DS21263,BMG_DS079903,episodic ataxia type 1
+BMGC_DS21264,BMG_DS079904,centronuclear myopathy 1
+BMGC_DS21265,BMG_DS079905,distal myopathy 1
+BMGC_DS21266,BMG_DS079906,Thomsen disease
+BMGC_DS21267,BMG_DS079908,nonsyndromic congenital nail disorder 1
+BMGC_DS21268,BMG_DS079909,nemaline myopathy 3
+BMGC_DS21269,BMG_DS079910,familial juvenile hyperuricemic nephropathy
+BMGC_DS21270,BMG_DS079911,hereditary sensory and autonomic neuropathy type 1A
+BMGC_DS21271,BMG_DS079912,stork bite
+BMGC_DS21272,BMG_DS079913,congenital nystagmus 2
+BMGC_DS21273,BMG_DS079914,spinocerebellar ataxia type 1
+BMGC_DS21274,BMG_DS079915,spinocerebellar ataxia type 7
+BMGC_DS21275,BMG_DS079916,nonsyndromic congenital nail disorder 5
+BMGC_DS21276,BMG_DS079918,optic atrophy 1
+BMGC_DS21277,BMG_DS079919,inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1
+BMGC_DS21278,BMG_DS079920,polycystic kidney disease 1
+BMGC_DS21279,BMG_DS079921,polycystic liver disease 1
+BMGC_DS21280,BMG_DS079922,preaxial polydactyly I
+BMGC_DS21281,BMG_DS079923,preaxial polydactyly II
+BMGC_DS21282,BMG_DS079924,preaxial polydactyly type IV
+BMGC_DS21283,BMG_DS079925,juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome
+BMGC_DS21284,BMG_DS079926,familial adenomatous polyposis 1
+BMGC_DS21285,BMG_DS079927,brain small vessel disease 1
+BMGC_DS21286,BMG_DS079928,punctate palmoplantar keratoderma type II
+BMGC_DS21287,BMG_DS079929,ITM2B-related cerebral amyloid angiopathy 1
+BMGC_DS21288,BMG_DS079930,psoriasis 1
+BMGC_DS21289,BMG_DS079931,"contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A"
+BMGC_DS21290,BMG_DS079932,retinal arterial tortuosity
+BMGC_DS21291,BMG_DS079933,schizophrenia 1
+BMGC_DS21292,BMG_DS079934,hereditary spherocytosis type 1
+BMGC_DS21293,BMG_DS079935,spinocerebellar ataxia type 6
+BMGC_DS21294,BMG_DS079936,spinocerebellar ataxia type 2
+BMGC_DS21295,BMG_DS079937,autosomal dominant spondyloepiphyseal dysplasia tarda
+BMGC_DS21296,BMG_DS079938,"spondyloepimetaphyseal dysplasia, Strudwick type"
+BMGC_DS21297,BMG_DS079939,"otospondylomegaepiphyseal dysplasia, autosomal dominant"
+BMGC_DS21298,BMG_DS079940,overhydrated hereditary stomatocytosis
+BMGC_DS21299,BMG_DS079941,syndactyly type 1
+BMGC_DS21300,BMG_DS079942,multiple synostoses syndrome 1
+BMGC_DS21301,BMG_DS079943,beta-thalassemia major | thalassemia minor
+BMGC_DS21302,BMG_DS079944,prothrombin thrombophilia
+BMGC_DS21303,BMG_DS079945,esophageal atresia/tracheoesophageal fistula
+BMGC_DS21304,BMG_DS079946,familial isolated trichomegaly
+BMGC_DS21305,BMG_DS079947,trichorhinophalangeal syndrome type III
+BMGC_DS21306,BMG_DS079948,uric acid urolithiasis
+BMGC_DS21307,BMG_DS079949,hypertrophic cardiomyopathy 1
+BMGC_DS21308,BMG_DS079950,autosomal dominant hypophosphatemic rickets
+BMGC_DS21309,BMG_DS079951,Watson syndrome
+BMGC_DS21310,BMG_DS079952,distal arthrogryposis type 2A
+BMGC_DS21311,BMG_DS079953,autosomal dominant woolly hair
+BMGC_DS21312,BMG_DS079954,acheiropody
+BMGC_DS21313,BMG_DS079955,achondrogenesis type IA
+BMGC_DS21314,BMG_DS079956,"acromesomelic dysplasia, Grebe type"
+BMGC_DS21315,BMG_DS079957,"acromesomelic dysplasia, Hunter-Thompson type"
+BMGC_DS21316,BMG_DS079958,hereditary sensory and autonomic neuropathy type 2A
+BMGC_DS21317,BMG_DS079959,short chain acyl-CoA dehydrogenase deficiency
+BMGC_DS21318,BMG_DS079960,very long chain acyl-CoA dehydrogenase deficiency
+BMGC_DS21319,BMG_DS079961,glucocorticoid deficiency 1
+BMGC_DS21320,BMG_DS079962,peroxisome biogenesis disorder 2B
+BMGC_DS21321,BMG_DS079963,severe congenital neutropenia 1
+BMGC_DS21322,BMG_DS079964,oculocutaneous albinism type IA
+BMGC_DS21323,BMG_DS079965,Hermansky-Pudlak syndrome 1
+BMGC_DS21324,BMG_DS079966,corticosterone methyloxidase deficiency 1
+BMGC_DS21325,BMG_DS079967,alopecia-mental retardation syndrome 1
+BMGC_DS21326,BMG_DS079968,2-aminoadipic 2-oxoadipic aciduria
+BMGC_DS21327,BMG_DS079969,juvenile amyotrophic lateral sclerosis with dementia
+BMGC_DS21328,BMG_DS079970,pyridoxine-responsive sideroblastic anemia
+BMGC_DS21329,BMG_DS079971,hypochromic microcytic anemia
+BMGC_DS21330,BMG_DS079972,Antley-Bixler syndrome without disordered steroidogenesis
+BMGC_DS21331,BMG_DS079973,"arthrogryposis, renal dysfunction, and cholestasis 1"
+BMGC_DS21332,BMG_DS079974,fetal akinesia deformation sequence syndrome 1
+BMGC_DS21333,BMG_DS079975,atransferrinemia
+BMGC_DS21334,BMG_DS079976,atrophoderma vermiculata
+BMGC_DS21335,BMG_DS079977,Elsahy-Waters syndrome
+BMGC_DS21336,BMG_DS079978,Fazio-Londe disease
+BMGC_DS21337,BMG_DS079979,Brown-Vialetto-Van Laere syndrome 1
+BMGC_DS21338,BMG_DS079980,hereditary arterial and articular multiple calcification syndrome
+BMGC_DS21339,BMG_DS079981,congenital disorder of glycosylation Ia
+BMGC_DS21340,BMG_DS079982,optic disc anomalies with retinal and/or macular dystrophy
+BMGC_DS21341,BMG_DS079983,Joubert syndrome 1
+BMGC_DS21342,BMG_DS079984,cerebrooculofacioskeletal syndrome 1
+BMGC_DS21343,BMG_DS079985,Klippel-Feil syndrome 2
+BMGC_DS21344,BMG_DS079986,metaphyseal dysplasia
+BMGC_DS21345,BMG_DS079987,classic citrullinemia
+BMGC_DS21346,BMG_DS079988,Cockayne syndrome A
+BMGC_DS21347,BMG_DS079989,congenital hereditary endothelial dystrophy of cornea
+BMGC_DS21348,BMG_DS079990,autosomal recessive craniometaphyseal dysplasia
+BMGC_DS21349,BMG_DS079991,ACTH-independent macronodular adrenal hyperplasia 1
+BMGC_DS21350,BMG_DS079992,autosomal-mitochondrial sensorineural deafness
+BMGC_DS21351,BMG_DS079993,combined pituitary hormone deficiency 3
+BMGC_DS21352,BMG_DS079994,familial erythrocytosis 8
+BMGC_DS21353,BMG_DS079995,Dyggve-Melchior-Clausen disease
+BMGC_DS21354,BMG_DS079996,"ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome"
+BMGC_DS21355,BMG_DS079997,Ehlers-Danlos syndrome cardiac valvular type
+BMGC_DS21356,BMG_DS079998,Ehlers-Danlos syndrome kyphoscoliotic type 1
+BMGC_DS21357,BMG_DS079999,Fanconi anemia complementation group A
+BMGC_DS21358,BMG_DS080000,infantile myofibromatosis
+BMGC_DS21359,BMG_DS080001,GM1 gangliosidosis type 1
+BMGC_DS21360,BMG_DS080002,GM1 gangliosidosis type 2
+BMGC_DS21361,BMG_DS080003,GM1 gangliosidosis type 3
+BMGC_DS21362,BMG_DS080004,GAPO syndrome
+BMGC_DS21363,BMG_DS080005,Gaucher's disease type IIIC
+BMGC_DS21364,BMG_DS080006,Ghosal hematodiaphyseal syndrome
+BMGC_DS21365,BMG_DS080007,triple-A syndrome
+BMGC_DS21366,BMG_DS080008,glutaric acidemia type 3
+BMGC_DS21367,BMG_DS080009,congenital nonspherocytic hemolytic anemia 6
+BMGC_DS21368,BMG_DS080010,glycogen storage disease Ia
+BMGC_DS21369,BMG_DS080011,glycogen storage disease Ib
+BMGC_DS21370,BMG_DS080012,ovarian dysgenesis 1
+BMGC_DS21371,BMG_DS080013,Perrault syndrome
+BMGC_DS21372,BMG_DS080014,"46,XY sex reversal 7"
+BMGC_DS21373,BMG_DS080015,autosomal recessive chronic granulomatous disease 1
+BMGC_DS21374,BMG_DS080016,autosomal recessive chronic granulomatous disease 2
+BMGC_DS21375,BMG_DS080017,BH4-deficient hyperphenylalaninemia B
+BMGC_DS21376,BMG_DS080018,nonphotosensitive trichothiodystrophy 4
+BMGC_DS21377,BMG_DS080019,holoprosencephaly 1
+BMGC_DS21378,BMG_DS080020,homocystinuria-megaloblastic anemia cblE type
+BMGC_DS21379,BMG_DS080021,"multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly"
+BMGC_DS21380,BMG_DS080022,congenital muscular dystrophy-dystroglycanopathy type A1
+BMGC_DS21381,BMG_DS080023,N-acetylglutamate synthase deficiency
+BMGC_DS21382,BMG_DS080024,Leydig cell hypoplasia type I
+BMGC_DS21383,BMG_DS080025,ornithine translocase deficiency
+BMGC_DS21384,BMG_DS080026,Paget's disease of bone 5
+BMGC_DS21385,BMG_DS080027,SOST-related sclerosing bone dysplasia
+BMGC_DS21386,BMG_DS080028,hyperprolinemia type 1
+BMGC_DS21387,BMG_DS080029,autoimmune polyendocrine syndrome type 1
+BMGC_DS21388,BMG_DS080030,leucine-sensitive hypoglycemia of infancy
+BMGC_DS21389,BMG_DS080031,infantile hypophosphatasia
+BMGC_DS21390,BMG_DS080032,childhood hypophosphatasia
+BMGC_DS21391,BMG_DS080033,autosomal recessive hypophosphatemic rickets
+BMGC_DS21392,BMG_DS080034,Bamforth-Lazarus syndrome
+BMGC_DS21393,BMG_DS080035,neuronal intestinal dysplasia type A
+BMGC_DS21394,BMG_DS080036,benign recurrent intrahepatic cholestasis 1
+BMGC_DS21395,BMG_DS080037,familial lipase maturation factor 1 deficiency
+BMGC_DS21396,BMG_DS080038,3MC syndrome 3
+BMGC_DS21397,BMG_DS080039,mandibuloacral dysplasia type A lipodystrophy
+BMGC_DS21398,BMG_DS080040,Treacher Collins syndrome 3
+BMGC_DS21399,BMG_DS080041,Marinesco-Sjogren syndrome
+BMGC_DS21400,BMG_DS080042,autosomal recessive intellectual developmental disorder 1
+BMGC_DS21401,BMG_DS080043,3-hydroxyisobutryl-CoA hydrolase deficiency
+BMGC_DS21402,BMG_DS080044,homocystinuria-megaloblastic anemia cblG type
+BMGC_DS21403,BMG_DS080045,primary autosomal recessive microcephaly 1
+BMGC_DS21404,BMG_DS080046,microcephaly-micromelia syndrome
+BMGC_DS21405,BMG_DS080047,orofaciodigital syndrome II
+BMGC_DS21406,BMG_DS080048,mucolipidosis II alpha/beta
+BMGC_DS21407,BMG_DS080049,mucolipidosis III alpha/beta
+BMGC_DS21408,BMG_DS080050,mucolipidosis type IV
+BMGC_DS21409,BMG_DS080051,Fukuyama congenital muscular dystrophy
+BMGC_DS21410,BMG_DS080052,Miyoshi muscular dystrophy 1
+BMGC_DS21411,BMG_DS080053,congenital myasthenic syndrome 6
+BMGC_DS21412,BMG_DS080054,congenital myasthenic syndrome 10
+BMGC_DS21413,BMG_DS080055,progressive myoclonus epilepsy 1A
+BMGC_DS21414,BMG_DS080056,autosomal recessive hyaline body myopathy
+BMGC_DS21415,BMG_DS080057,Becker disease
+BMGC_DS21416,BMG_DS080058,congenital myopathy 4A
+BMGC_DS21417,BMG_DS080059,congenital myopathy 1B
+BMGC_DS21418,BMG_DS080060,nephronophthisis 1
+BMGC_DS21419,BMG_DS080061,familial hyperinsulinemic hypoglycemia 1
+BMGC_DS21420,BMG_DS080062,atypical hereditary sensory neuropathy
+BMGC_DS21421,BMG_DS080063,mosaic variegated aneuploidy syndrome 1
+BMGC_DS21422,BMG_DS080064,"ocular motor apraxia, Cogan type"
+BMGC_DS21423,BMG_DS080065,3MC syndrome 1
+BMGC_DS21424,BMG_DS080066,bladder exstrophy-epispadias-cloacal exstrophy complex | cloacal exstrophy
+BMGC_DS21425,BMG_DS080067,Oguchi disease-1
+BMGC_DS21426,BMG_DS080068,spermatogenic failure 1
+BMGC_DS21427,BMG_DS080069,3-methylglutaconic aciduria type 3
+BMGC_DS21428,BMG_DS080070,autosomal recessive osteopetrosis 1
+BMGC_DS21429,BMG_DS080071,autosomal recessive osteopetrosis 2
+BMGC_DS21430,BMG_DS080072,autosomal recessive osteopetrosis 5
+BMGC_DS21431,BMG_DS080073,Parkinson's disease 15
+BMGC_DS21432,BMG_DS080074,hyperimmunoglobulinemia D periodic fever syndrome
+BMGC_DS21433,BMG_DS080075,congenital intrinsic factor deficiency
+BMGC_DS21434,BMG_DS080076,Peters plus syndrome
+BMGC_DS21435,BMG_DS080077,BH4-deficient hyperphenylalaninemia C
+BMGC_DS21436,BMG_DS080078,combined pituitary hormone deficiency 2
+BMGC_DS21437,BMG_DS080079,polycystic kidney disease 4
+BMGC_DS21438,BMG_DS080080,BH4-deficient hyperphenylalaninemia D
+BMGC_DS21439,BMG_DS080081,Wiedemann-Rautenstrauch syndrome
+BMGC_DS21440,BMG_DS080082,vitamin D-dependent rickets type 1A
+BMGC_DS21441,BMG_DS080083,3MC syndrome 2
+BMGC_DS21442,BMG_DS080084,congenital nonspherocytic hemolytic anemia 8
+BMGC_DS21443,BMG_DS080085,glutatione synthetase deficiency with 5-oxoprolinuria
+BMGC_DS21444,BMG_DS080086,inflammatory bowel disease 1
+BMGC_DS21445,BMG_DS080087,familial hemophagocytic lymphohistiocytosis 1
+BMGC_DS21446,BMG_DS080088,Revesz syndrome
+BMGC_DS21447,BMG_DS080089,autoimmune polyendocrine syndrome type 2
+BMGC_DS21448,BMG_DS080090,spermatogenic failure 4
+BMGC_DS21449,BMG_DS080091,hereditary spherocytosis type 3
+BMGC_DS21450,BMG_DS080092,autosomal recessive spondyloepiphyseal dysplasia tarda
+BMGC_DS21451,BMG_DS080093,spondyloperipheral dysplasia
+BMGC_DS21452,BMG_DS080094,Sugarman brachydactyly
+BMGC_DS21453,BMG_DS080095,cold-induced sweating syndrome 1
+BMGC_DS21454,BMG_DS080096,transcobalamin II deficiency
+BMGC_DS21455,BMG_DS080097,Chanarin-Dorfman syndrome
+BMGC_DS21456,BMG_DS080098,mismatch repair cancer syndrome
+BMGC_DS21457,BMG_DS080099,tyrosinemia type II
+BMGC_DS21458,BMG_DS080100,tyrosinemia type I
+BMGC_DS21459,BMG_DS080101,tyrosinemia type III
+BMGC_DS21460,BMG_DS080102,Schinzel type phocomelia
+BMGC_DS21461,BMG_DS080103,Mayer-Rokitansky-Kuster-Hauser syndrome type 1
+BMGC_DS21462,BMG_DS080104,autosomal recessive congenital bilateral absence of vas deferens
+BMGC_DS21463,BMG_DS080105,spondylocostal dysostosis 1
+BMGC_DS21464,BMG_DS080106,methylmalonic aciduria and homocystinuria type cblF
+BMGC_DS21465,BMG_DS080107,methylmalonic aciduria and homocystinuria type cblD
+BMGC_DS21466,BMG_DS080108,vitamin D-dependent rickets type 2A
+BMGC_DS21467,BMG_DS080109,autosomal recessive Whistling face syndrome
+BMGC_DS21468,BMG_DS080110,Opitz GBBB syndrome
+BMGC_DS21469,BMG_DS080111,corpus callosum agenesis-abnormal genitalia syndrome
+BMGC_DS21470,BMG_DS080112,X-linked deafness 3
+BMGC_DS21471,BMG_DS080113,non-syndromic X-linked intellectual disability 23
+BMGC_DS21472,BMG_DS080114,non-syndromic X-linked intellectual disability 20
+BMGC_DS21473,BMG_DS080115,non-syndromic X-linked intellectual disability 14
+BMGC_DS21474,BMG_DS080116,X-linked deafness 4
+BMGC_DS21475,BMG_DS080117,fetal akinesia deformation sequence syndrome X-linked
+BMGC_DS21476,BMG_DS080118,X-linked adrenal hypoplasia congenita
+BMGC_DS21477,BMG_DS080119,Simpson-Golabi-Behmel syndrome type 2
+BMGC_DS21478,BMG_DS080120,X-linked lissencephaly 2
+BMGC_DS21479,BMG_DS080121,non-syndromic X-linked intellectual disability 72
+BMGC_DS21480,BMG_DS080122,ectodermal dysplasia and immunodeficiency 1
+BMGC_DS21481,BMG_DS080123,HRPT-related hyperuricemia
+BMGC_DS21482,BMG_DS080124,non-syndromic X-linked intellectual disability 53
+BMGC_DS21483,BMG_DS080125,cerebral creatine deficiency syndrome 1
+BMGC_DS21484,BMG_DS080126,non-syndromic X-linked intellectual disability 73
+BMGC_DS21485,BMG_DS080127,non-syndromic X-linked intellectual disability 42
+BMGC_DS21486,BMG_DS080128,non-syndromic X-linked intellectual disability 63
+BMGC_DS21487,BMG_DS080129,non-syndromic X-linked intellectual disability 2
+BMGC_DS21488,BMG_DS080130,non-syndromic X-linked intellectual disability 81
+BMGC_DS21489,BMG_DS080131,Stocco Dos Santos type X-linked intellectual disability
+BMGC_DS21490,BMG_DS080132,non-syndromic X-linked intellectual disability 46
+BMGC_DS21491,BMG_DS080133,non-syndromic X-linked intellectual disability 77
+BMGC_DS21492,BMG_DS080134,X-linked retinitis pigmentosa and sinorespiratory infections
+BMGC_DS21493,BMG_DS080135,X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance
+BMGC_DS21494,BMG_DS080136,non-syndromic X-linked intellectual disability 45
+BMGC_DS21495,BMG_DS080137,non-syndromic X-linked intellectual disability 84
+BMGC_DS21496,BMG_DS080138,primary ovarian insufficiency 4
+BMGC_DS21497,BMG_DS080139,primary ovarian insufficiency 2A
+BMGC_DS21498,BMG_DS080140,non-syndromic X-linked intellectual disability 82
+BMGC_DS21499,BMG_DS080141,X-linked recessive hypophosphatemic rickets
+BMGC_DS21500,BMG_DS080142,non-syndromic X-linked intellectual disability 91
+BMGC_DS21501,BMG_DS080143,X-linked congenital myopathy with fiber-type disproportion
+BMGC_DS21502,BMG_DS080144,SHOX-related short stature
+BMGC_DS21503,BMG_DS080145,congenital nystagmus 5
+BMGC_DS21504,BMG_DS080146,Cornelia de Lange syndrome 2
+BMGC_DS21505,BMG_DS080147,primary ovarian insufficiency 2B
+BMGC_DS21506,BMG_DS080148,developmental and epileptic encephalopathy 8
+BMGC_DS21507,BMG_DS080149,X-linked deafness 5
+BMGC_DS21508,BMG_DS080150,Tn polyagglutination syndrome
+BMGC_DS21509,BMG_DS080151,developmental and epileptic encephalopathy 2
+BMGC_DS21510,BMG_DS080152,X-linked Emery-Dreifuss muscular dystrophy 6
+BMGC_DS21511,BMG_DS080153,non-syndromic X-linked intellectual disability
+BMGC_DS21512,BMG_DS080154,sideroblastic anemia 1
+BMGC_DS21513,BMG_DS080155,Alzheimer's disease 16
+BMGC_DS21514,BMG_DS080156,non-syndromic X-linked intellectual disability 97
+BMGC_DS21515,BMG_DS080157,non-syndromic X-linked intellectual disability 89
+BMGC_DS21516,BMG_DS080158,non-syndromic X-linked intellectual disability 90
+BMGC_DS21517,BMG_DS080159,non-syndromic X-linked intellectual disability 92
+BMGC_DS21518,BMG_DS080160,"X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia"
+BMGC_DS21519,BMG_DS080161,Ogden syndrome
+BMGC_DS21520,BMG_DS080162,syndromic X-linked intellectual disability 17
+BMGC_DS21521,BMG_DS080163,syndromic X-linked intellectual disability Chudley-Schwartz type
+BMGC_DS21522,BMG_DS080164,intracranial berry aneurysm 5
+BMGC_DS21523,BMG_DS080165,developmental and epileptic encephalopathy 36
+BMGC_DS21524,BMG_DS080166,congenital disorder of glycosylation type IIm
+BMGC_DS21525,BMG_DS080167,non-syndromic X-linked intellectual disability 99
+BMGC_DS21526,BMG_DS080168,congenital disorder of glycosylation Iy
+BMGC_DS21527,BMG_DS080169,growth hormone secreting pituitary adenoma 2
+BMGC_DS21528,BMG_DS080170,syndromic X-linked intellectual disability 34
+BMGC_DS21529,BMG_DS080171,immunodeficiency 50
+BMGC_DS21530,BMG_DS080172,non-syndromic X-linked intellectual disability 106
+BMGC_DS21531,BMG_DS080173,syndromic X-linked mental retardation Hough type
+BMGC_DS21532,BMG_DS080174,non-syndromic X-linked intellectual disability 107
+BMGC_DS21533,BMG_DS080175,osteogenesis imperfecta type 19
+BMGC_DS21534,BMG_DS080176,Van Esch-O'Driscoll syndrome
+BMGC_DS21535,BMG_DS080177,X-linked warfarin sensitivity
+BMGC_DS21536,BMG_DS080178,VEXAS syndrome
+BMGC_DS21537,BMG_DS080179,syndromic X-linked intellectual disability Pilorge type
+BMGC_DS21538,BMG_DS080180,congenital nonspherocytic hemolytic anemia 9
+BMGC_DS21539,BMG_DS080181,non-syndromic X-linked intellectual developmental disorder 111
+BMGC_DS21540,BMG_DS080182,neural tube defect
+BMGC_DS21541,BMG_DS080183,X-linked chondrodysplasia punctata 2
+BMGC_DS21542,BMG_DS080184,X-linked cleft palate with or without ankyloglossia
+BMGC_DS21543,BMG_DS080185,X-linked deafness 2
+BMGC_DS21544,BMG_DS080186,X-linked deafness 1
+BMGC_DS21545,BMG_DS080187,X-linked nephrogenic diabetes insipidus
+BMGC_DS21546,BMG_DS080188,X-linked exudative vitreoretinopathy 2
+BMGC_DS21547,BMG_DS080189,frontometaphyseal dysplasia 1
+BMGC_DS21548,BMG_DS080190,X-linked spermatogenic failure 1
+BMGC_DS21549,BMG_DS080191,X-linked chronic granulomatous disease
+BMGC_DS21550,BMG_DS080192,visceral heterotaxy
+BMGC_DS21551,BMG_DS080193,X-linked hypoparathyroidism
+BMGC_DS21552,BMG_DS080194,CD40 ligand deficiency
+BMGC_DS21553,BMG_DS080195,X-linked keratosis follicularis spinulosa decalvans
+BMGC_DS21554,BMG_DS080196,low molecular weight proteinuria with hypercalciuric nephrocalcinosis
+BMGC_DS21555,BMG_DS080197,syndromic X-linked intellectual disorder Lujan-Fryns-type
+BMGC_DS21556,BMG_DS080198,X-linked intellectual developmental disorder 109
+BMGC_DS21557,BMG_DS080199,non-syndromic X-linked intellectual disability 9
+BMGC_DS21558,BMG_DS080200,X-linked mental retardation Gustavson type
+BMGC_DS21559,BMG_DS080201,Prieto syndrome
+BMGC_DS21560,BMG_DS080202,X-linked Emery-Dreifuss muscular dystrophy 1
+BMGC_DS21561,BMG_DS080203,X-linked myopathy with excessive autophagy
+BMGC_DS21562,BMG_DS080204,X-linked nephrolithiasis type I
+BMGC_DS21563,BMG_DS080205,hereditary sensory neuropathy X-linked
+BMGC_DS21564,BMG_DS080206,congenital stationary night blindness 1A
+BMGC_DS21565,BMG_DS080207,congenital nystagmus 1
+BMGC_DS21566,BMG_DS080208,optic atrophy 2
+BMGC_DS21567,BMG_DS080209,primary ovarian insufficiency 1
+BMGC_DS21568,BMG_DS080210,Waisman syndrome
+BMGC_DS21569,BMG_DS080211,X-linked panhypopituitarism
+BMGC_DS21570,BMG_DS080212,partial androgen insensitivity syndrome
+BMGC_DS21571,BMG_DS080213,X-linked spondyloepiphyseal dysplasia tarda
+BMGC_DS21572,BMG_DS080214,Y-linked spermatogenic failure 1
+BMGC_DS21573,BMG_DS080215,"46,XY sex reversal 1"
+BMGC_DS21574,BMG_DS080216,"46,XX sex reversal 1"
+BMGC_DS21575,BMG_DS080217,infantile histiocytoid cardiomyopathy
+BMGC_DS21576,BMG_DS080218,Pearson syndrome
+BMGC_DS21577,BMG_DS080219,pancreatic hypoplasia-diabetes-congenital heart disease syndrome
+BMGC_DS21578,BMG_DS080220,familial chronic myelocytic leukemia-like syndrome
+BMGC_DS21579,BMG_DS080221,vitamin D-dependent rickets type 1B
+BMGC_DS21580,BMG_DS080222,nanophthalmos
+BMGC_DS21581,BMG_DS080223,autosomal dominant distal hereditary motor neuronopathy 8
+BMGC_DS21582,BMG_DS080224,multiple epiphyseal dysplasia 2
+BMGC_DS21583,BMG_DS080225,spinocerebellar ataxia type 5
+BMGC_DS21584,BMG_DS080226,oblique facial clefting 1
+BMGC_DS21585,BMG_DS080227,CSF1R-related brain malformation and osteopetrosis
+BMGC_DS21586,BMG_DS080228,Charcot-Marie-Tooth disease type 5
+BMGC_DS21587,BMG_DS080229,maturity-onset diabetes of the young type 3
+BMGC_DS21588,BMG_DS080230,schizophrenia 3
+BMGC_DS21589,BMG_DS080231,familial temporal lobe epilepsy 1
+BMGC_DS21590,BMG_DS080232,autosomal dominant nocturnal frontal lobe epilepsy 1
+BMGC_DS21591,BMG_DS080233,vitamin D-dependent rickets type 2B
+BMGC_DS21592,BMG_DS080234,janus kinase-3 deficiency
+BMGC_DS21593,BMG_DS080235,hypertrophic cardiomyopathy 6
+BMGC_DS21594,BMG_DS080236,achondrogenesis type IB
+BMGC_DS21595,BMG_DS080237,Mayer-Rokitansky-Kuster-Hauser syndrome type 2
+BMGC_DS21596,BMG_DS080238,Charcot-Marie-Tooth disease type 6
+BMGC_DS21597,BMG_DS080239,DICER1 syndrome
+BMGC_DS21598,BMG_DS080240,neuronal intestinal dysplasia type B
+BMGC_DS21599,BMG_DS080241,diffuse cystic renal dysplasia
+BMGC_DS21600,BMG_DS080242,Nicolaides-Baraitser syndrome
+BMGC_DS21601,BMG_DS080243,psoriasis 3
+BMGC_DS21602,BMG_DS080244,mucopolysaccharidosis IX
+BMGC_DS21603,BMG_DS080245,Athabaskan brainstem dysgenesis syndrome
+BMGC_DS21604,BMG_DS080246,peroxisome biogenesis disorder 1B
+BMGC_DS21605,BMG_DS080247,photosensitive trichothiodystrophy 1
+BMGC_DS21606,BMG_DS080248,benign familial infantile seizures 1
+BMGC_DS21607,BMG_DS080249,Ehlers-Danlos syndrome musculocontractural type 1
+BMGC_DS21608,BMG_DS080250,cone-rod dystrophy 6
+BMGC_DS21609,BMG_DS080251,familial hyperinsulinemic hypoglycemia 2
+BMGC_DS21610,BMG_DS080252,ectodermal dysplasia 4
+BMGC_DS21611,BMG_DS080253,speech-language disorder-1
+BMGC_DS21612,BMG_DS080254,amyotrophic lateral sclerosis type 5
+BMGC_DS21613,BMG_DS080255,Pierpont syndrome
+BMGC_DS21614,BMG_DS080256,Parkinson's disease 3
+BMGC_DS21615,BMG_DS080257,familial hyperinsulinemic hypoglycemia 3
+BMGC_DS21616,BMG_DS080258,congenital disorder of glycosylation Ib
+BMGC_DS21617,BMG_DS080259,"spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability"
+BMGC_DS21618,BMG_DS080260,histiocytosis-lymphadenopathy plus syndrome
+BMGC_DS21619,BMG_DS080261,congenital myasthenic syndrome 5
+BMGC_DS21620,BMG_DS080262,age related macular degeneration 1
+BMGC_DS21621,BMG_DS080263,congenital disorder of glycosylation Ic
+BMGC_DS21622,BMG_DS080264,schizophrenia 5
+BMGC_DS21623,BMG_DS080265,schizophrenia 7
+BMGC_DS21624,BMG_DS080266,autosomal dominant nocturnal frontal lobe epilepsy 2
+BMGC_DS21625,BMG_DS080267,schizophrenia 8
+BMGC_DS21626,BMG_DS080268,familial gestational hyperthyroidism
+BMGC_DS21627,BMG_DS080269,adult-onset type II citrullinemia
+BMGC_DS21628,BMG_DS080270,neuronal intranuclear inclusion disease
+BMGC_DS21629,BMG_DS080271,spinocerebellar ataxia type 10
+BMGC_DS21630,BMG_DS080272,congenital chylothorax
+BMGC_DS21631,BMG_DS080273,spondyloepimetaphyseal dysplasia with joint laxity type 2
+BMGC_DS21632,BMG_DS080274,familial hemophagocytic lymphohistiocytosis 4
+BMGC_DS21633,BMG_DS080275,myofibrillar myopathy 9
+BMGC_DS21634,BMG_DS080276,autosomal dominant beta thalassemia
+BMGC_DS21635,BMG_DS080277,sickle cell disease
+BMGC_DS21636,BMG_DS080278,psoriasis 4
+BMGC_DS21637,BMG_DS080279,keratosis pilaris atrophicans
+BMGC_DS21638,BMG_DS080280,left ventricular noncompaction
+BMGC_DS21639,BMG_DS080281,aceruloplasminemia
+BMGC_DS21640,BMG_DS080282,psoriasis 5
+BMGC_DS21641,BMG_DS080283,spinocerebellar ataxia type 12
+BMGC_DS21642,BMG_DS080284,familial febrile seizures 4
+BMGC_DS21643,BMG_DS080285,ataxia-telangiectasia-like disorder-1
+BMGC_DS21644,BMG_DS080286,PAPA syndrome
+BMGC_DS21645,BMG_DS080287,infundibulocystic basal cell carcinoma
+BMGC_DS21646,BMG_DS080288,MHC class I deficiency
+BMGC_DS21647,BMG_DS080289,craniosynostosis 2
+BMGC_DS21648,BMG_DS080290,primary autosomal recessive microcephaly 3
+BMGC_DS21649,BMG_DS080291,Stickler syndrome 2
+BMGC_DS21650,BMG_DS080292,schizophrenia 9
+BMGC_DS21651,BMG_DS080293,familial hypobetalipoproteinemia 2
+BMGC_DS21652,BMG_DS080294,spinocerebellar ataxia type 13
+BMGC_DS21653,BMG_DS080295,spinocerebellar ataxia type 14
+BMGC_DS21654,BMG_DS080296,dilated cardiomyopathy 1J
+BMGC_DS21655,BMG_DS080297,psoriasis 6
+BMGC_DS21656,BMG_DS080298,autosomal dominant nocturnal frontal lobe epilepsy 3
+BMGC_DS21657,BMG_DS080299,ataxic cerebral palsy
+BMGC_DS21658,BMG_DS080300,schizophrenia 10
+BMGC_DS21659,BMG_DS080301,psoriasis 7
+BMGC_DS21660,BMG_DS080302,congenital myopathy 6
+BMGC_DS21661,BMG_DS080303,multiple mitochondrial dysfunctions syndrome 1
+BMGC_DS21662,BMG_DS080304,platelet-type bleeding disorder 12
+BMGC_DS21663,BMG_DS080305,atopic dermatitis 2
+BMGC_DS21664,BMG_DS080306,atopic dermatitis 3
+BMGC_DS21665,BMG_DS080307,atopic dermatitis 5
+BMGC_DS21666,BMG_DS080308,atopic dermatitis 6
+BMGC_DS21667,BMG_DS080309,dimethylglycine dehydrogenase deficiency
+BMGC_DS21668,BMG_DS080310,glycine encephalopathy 1
+BMGC_DS21669,BMG_DS080311,Parkinson's disease 6
+BMGC_DS21670,BMG_DS080312,HMG-CoA synthase 2 deficiency
+BMGC_DS21671,BMG_DS080313,spinocerebellar ataxia with axonal neuropathy 2
+BMGC_DS21672,BMG_DS080314,Phelan-McDermid syndrome
+BMGC_DS21673,BMG_DS080315,maturity-onset diabetes of the young type 6
+BMGC_DS21674,BMG_DS080316,Ehlers-Danlos syndrome classic-like 1
+BMGC_DS21675,BMG_DS080317,episodic ataxia type 3
+BMGC_DS21676,BMG_DS080318,oculocutaneous albinism type IV
+BMGC_DS21677,BMG_DS080319,DNA ligase IV deficiency
+BMGC_DS21678,BMG_DS080320,amyotrophic lateral sclerosis type 3
+BMGC_DS21679,BMG_DS080321,Waardenburg syndrome type 2C
+BMGC_DS21680,BMG_DS080322,specific language impairment
+BMGC_DS21681,BMG_DS080323,familial hyperinsulinemic hypoglycemia 6
+BMGC_DS21682,BMG_DS080325,brachydactyly type A1B
+BMGC_DS21683,BMG_DS080326,congenital disorder of glycosylation Ig
+BMGC_DS21684,BMG_DS080327,Dravet syndrome
+BMGC_DS21685,BMG_DS080328,spinocerebellar ataxia type 19/22
+BMGC_DS21686,BMG_DS080329,autosomal recessive intellectual developmental disorder 2
+BMGC_DS21687,BMG_DS080330,lissencephaly 1
+BMGC_DS21688,BMG_DS080331,Newfoundland cone-rod dystrophy
+BMGC_DS21689,BMG_DS080332,familial atrial fibrillation
+BMGC_DS21690,BMG_DS080333,pontocerebellar hypoplasia type 1A
+BMGC_DS21691,BMG_DS080334,idiopathic generalized epilepsy 11
+BMGC_DS21692,BMG_DS080335,juvenile absence epilepsy 1
+BMGC_DS21693,BMG_DS080336,autosomal dominant distal hereditary motor neuronopathy 14
+BMGC_DS21694,BMG_DS080337,idiopathic generalized epilepsy 9
+BMGC_DS21695,BMG_DS080338,Alzheimer's disease 3
+BMGC_DS21696,BMG_DS080339,focal segmental glomerulosclerosis 3
+BMGC_DS21697,BMG_DS080340,psoriasis 9
+BMGC_DS21698,BMG_DS080341,familial adult myoclonic epilepsy 2
+BMGC_DS21699,BMG_DS080342,amyotrophic lateral sclerosis type 6
+BMGC_DS21700,BMG_DS080343,amyotrophic lateral sclerosis type 7
+BMGC_DS21701,BMG_DS080344,congenital disorder of glycosylation Ij
+BMGC_DS21702,BMG_DS080345,congenital disorder of glycosylation Ih
+BMGC_DS21703,BMG_DS080346,Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
+BMGC_DS21704,BMG_DS080347,Kagami-Ogata syndrome
+BMGC_DS21705,BMG_DS080348,congenital nystagmus 3
+BMGC_DS21706,BMG_DS080349,autosomal dominant hyaline body myopathy
+BMGC_DS21707,BMG_DS080350,primary autosomal recessive microcephaly 6
+BMGC_DS21708,BMG_DS080351,platelet-type bleeding disorder 10
+BMGC_DS21709,BMG_DS080352,bradyopsia 1
+BMGC_DS21710,BMG_DS080353,autosomal recessive intellectual developmental disorder 3
+BMGC_DS21711,BMG_DS080354,congenital disorder of glycosylation Ik
+BMGC_DS21712,BMG_DS080355,intracranial berry aneurysm 2
+BMGC_DS21713,BMG_DS080356,amyotrophic lateral sclerosis type 8
+BMGC_DS21714,BMG_DS080357,autosomal dominant distal hereditary motor neuronopathy 3
+BMGC_DS21715,BMG_DS080358,spondylocostal dysostosis 2
+BMGC_DS21716,BMG_DS080359,primary autosomal recessive microcephaly 5
+BMGC_DS21717,BMG_DS080360,idiopathic generalized epilepsy 3
+BMGC_DS21718,BMG_DS080361,congenital disorder of glycosylation Il
+BMGC_DS21719,BMG_DS080362,myofibrillar myopathy 2
+BMGC_DS21720,BMG_DS080363,orofacial cleft 6
+BMGC_DS21721,BMG_DS080364,Alzheimer's disease 9
+BMGC_DS21722,BMG_DS080365,congenital myasthenic syndrome 4C
+BMGC_DS21723,BMG_DS080366,patterned macular dystrophy 2
+BMGC_DS21724,BMG_DS080367,autosomal dominant sensory ataxia 1
+BMGC_DS21725,BMG_DS080368,primary ovarian insufficiency 3
+BMGC_DS21726,BMG_DS080369,cataract 28
+BMGC_DS21727,BMG_DS080370,salt and pepper syndrome
+BMGC_DS21728,BMG_DS080371,nonautoimmune hyperthyroidism
+BMGC_DS21729,BMG_DS080372,Loeys-Dietz syndrome 1
+BMGC_DS21730,BMG_DS080373,autosomal recessive spondyloepiphyseal dysplasia tarda Leroy-Spranger type
+BMGC_DS21731,BMG_DS080374,Schindler disease type 1
+BMGC_DS21732,BMG_DS080375,Kanzaki disease
+BMGC_DS21733,BMG_DS080376,familial febrile seizures 6
+BMGC_DS21734,BMG_DS080377,familial febrile seizures 5
+BMGC_DS21735,BMG_DS080378,autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2
+BMGC_DS21736,BMG_DS080379,autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3
+BMGC_DS21737,BMG_DS080380,developmental and epileptic encephalopathy 3
+BMGC_DS21738,BMG_DS080381,hereditary nonpolyposis colorectal cancer type 2
+BMGC_DS21739,BMG_DS080382,MEDNIK syndrome
+BMGC_DS21740,BMG_DS080383,rhabdoid tumor predisposition syndrome 1
+BMGC_DS21741,BMG_DS080384,congenital fibrosis of the extraocular muscles 3C
+BMGC_DS21742,BMG_DS080385,myofibrillar myopathy 5
+BMGC_DS21743,BMG_DS080386,restrictive cardiomyopathy 2
+BMGC_DS21744,BMG_DS080387,short QT syndrome
+BMGC_DS21745,BMG_DS080388,autosomal dominant familial visceral neuropathy
+BMGC_DS21746,BMG_DS080389,familial hemiplegic migraine 3
+BMGC_DS21747,BMG_DS080391,generalized epilepsy with febrile seizures plus 4
+BMGC_DS21748,BMG_DS080392,spondylocostal dysostosis 3
+BMGC_DS21749,BMG_DS080393,familial erythrocytosis 3
+BMGC_DS21750,BMG_DS080394,familial hyperinsulinemic hypoglycemia 5
+BMGC_DS21751,BMG_DS080395,familial hyperinsulinemic hypoglycemia 4
+BMGC_DS21752,BMG_DS080396,congenital glutamine deficiency
+BMGC_DS21753,BMG_DS080397,hereditary mixed polyposis syndrome 2
+BMGC_DS21754,BMG_DS080398,distal myopathy 3
+BMGC_DS21755,BMG_DS080399,giant axonal neuropathy 2
+BMGC_DS21756,BMG_DS080400,autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4
+BMGC_DS21757,BMG_DS080401,age related macular degeneration 7
+BMGC_DS21758,BMG_DS080402,Loeys-Dietz syndrome 2
+BMGC_DS21759,BMG_DS080403,3-methylglutaconic aciduria type 5
+BMGC_DS21760,BMG_DS080404,neonatal diabetes mellitus with congenital hypothyroidism
+BMGC_DS21761,BMG_DS080405,intracranial berry aneurysm 4
+BMGC_DS21762,BMG_DS080406,hereditary spastic paraplegia 33
+BMGC_DS21763,BMG_DS080407,anterior segment dysgenesis 2
+BMGC_DS21764,BMG_DS080408,cold-induced sweating syndrome 2
+BMGC_DS21765,BMG_DS080409,Koolen de Vries syndrome
+BMGC_DS21766,BMG_DS080410,congenital stationary night blindness autosomal dominant 3
+BMGC_DS21767,BMG_DS080411,congenital stationary night blindness autosomal dominant 1
+BMGC_DS21768,BMG_DS080412,normophosphatemic familial tumoral calcinosis
+BMGC_DS21769,BMG_DS080413,poor metabolism of thiopurines 1
+BMGC_DS21770,BMG_DS080414,maturity-onset diabetes of the young type 7
+BMGC_DS21771,BMG_DS080415,"mandibulofacial dysostosis, Guion-Almeida type"
+BMGC_DS21772,BMG_DS080416,age related macular degeneration 4
+BMGC_DS21773,BMG_DS080417,psoriasis 8
+BMGC_DS21774,BMG_DS080418,severe congenital neutropenia 3
+BMGC_DS21775,BMG_DS080419,Cornelia de Lange syndrome 3
+BMGC_DS21776,BMG_DS080420,congenital disorder of glycosylation Im
+BMGC_DS21777,BMG_DS080421,CAKUT1
+BMGC_DS21778,BMG_DS080422,branchiootorenal syndrome 2
+BMGC_DS21779,BMG_DS080423,PSAT deficiency
+BMGC_DS21780,BMG_DS080424,autosomal recessive intellectual developmental disorder 12
+BMGC_DS21781,BMG_DS080425,autosomal recessive intellectual developmental disorder 5
+BMGC_DS21782,BMG_DS080426,autosomal recessive intellectual developmental disorder 6
+BMGC_DS21783,BMG_DS080427,autosomal recessive intellectual developmental disorder 7
+BMGC_DS21784,BMG_DS080428,autosomal recessive intellectual developmental disorder 9/26
+BMGC_DS21785,BMG_DS080429,autosomal recessive intellectual developmental disorder 10/20
+BMGC_DS21786,BMG_DS080430,autosomal recessive intellectual developmental disorder 11
+BMGC_DS21787,BMG_DS080431,autosomal recessive intellectual developmental disorder 4
+BMGC_DS21788,BMG_DS080432,idiopathic generalized epilepsy 13
+BMGC_DS21789,BMG_DS080433,syndromic microphthalmia 10
+BMGC_DS21790,BMG_DS080434,spastic ataxia 2
+BMGC_DS21791,BMG_DS080435,lethal congenital contracture syndrome 3
+BMGC_DS21792,BMG_DS080436,age related macular degeneration 9
+BMGC_DS21793,BMG_DS080437,spastic ataxia 3
+BMGC_DS21794,BMG_DS080438,essential tremor 3
+BMGC_DS21795,BMG_DS080439,age related macular degeneration 10
+BMGC_DS21796,BMG_DS080440,autosomal recessive osteopetrosis 4
+BMGC_DS21797,BMG_DS080441,autosomal recessive osteopetrosis 6
+BMGC_DS21798,BMG_DS080442,familial febrile seizures 7
+BMGC_DS21799,BMG_DS080443,primary ovarian insufficiency 5
+BMGC_DS21800,BMG_DS080444,familial temporal lobe epilepsy 3
+BMGC_DS21801,BMG_DS080445,familial temporal lobe epilepsy 4
+BMGC_DS21802,BMG_DS080446,familial febrile seizures 9
+BMGC_DS21803,BMG_DS080448,congenital myopathy 5
+BMGC_DS21804,BMG_DS080449,familial erythrocytosis 4
+BMGC_DS21805,BMG_DS080450,intracranial berry aneurysm 6
+BMGC_DS21806,BMG_DS080451,amyotrophic lateral sclerosis type 9
+BMGC_DS21807,BMG_DS080452,episodic ataxia type 7
+BMGC_DS21808,BMG_DS080454,age related macular degeneration 11
+BMGC_DS21809,BMG_DS080455,congenital disorder of glycosylation In
+BMGC_DS21810,BMG_DS080456,otosclerosis 8
+BMGC_DS21811,BMG_DS080457,hypertrophic cardiomyopathy 11
+BMGC_DS21812,BMG_DS080458,ectodermal dysplasia and immunodeficiency 2
+BMGC_DS21813,BMG_DS080459,intracranial berry aneurysm 7
+BMGC_DS21814,BMG_DS080460,intracranial berry aneurysm 8
+BMGC_DS21815,BMG_DS080461,developmental and epileptic encephalopathy 4
+BMGC_DS21816,BMG_DS080462,maturity-onset diabetes of the young type 9
+BMGC_DS21817,BMG_DS080463,Crouzon syndrome-acanthosis nigricans syndrome
+BMGC_DS21818,BMG_DS080464,generalized epilepsy with febrile seizures plus 6
+BMGC_DS21819,BMG_DS080465,primary ovarian insufficiency 6
+BMGC_DS21820,BMG_DS080466,autosomal dominant intellectual developmental disorder 22
+BMGC_DS21821,BMG_DS080467,Ehlers-Danlos syndrome spondylodysplastic type 3
+BMGC_DS21822,BMG_DS080468,congenital disorder of glycosylation Iq
+BMGC_DS21823,BMG_DS080469,psoriasis 10
+BMGC_DS21824,BMG_DS080470,restrictive cardiomyopathy 3
+BMGC_DS21825,BMG_DS080471,progressive myoclonus epilepsy 1B
+BMGC_DS21826,BMG_DS080472,pseudohypoparathyroidism type 1C
+BMGC_DS21827,BMG_DS080473,Compton-North congenital myopathy
+BMGC_DS21828,BMG_DS080474,severe congenital neutropenia 4
+BMGC_DS21829,BMG_DS080475,autosomal dominant intellectual developmental disorder 3
+BMGC_DS21830,BMG_DS080476,autosomal dominant intellectual developmental disorder 4
+BMGC_DS21831,BMG_DS080477,intracranial berry aneurysm 9
+BMGC_DS21832,BMG_DS080478,intracranial berry aneurysm 10
+BMGC_DS21833,BMG_DS080479,psoriasis 11
+BMGC_DS21834,BMG_DS080480,autosomal dominant intellectual developmental disorder 5
+BMGC_DS21835,BMG_DS080481,benign familial infantile seizures 4
+BMGC_DS21836,BMG_DS080482,congenital nonspherocytic hemolytic anemia 3
+BMGC_DS21837,BMG_DS080483,familial febrile seizures 10
+BMGC_DS21838,BMG_DS080484,hereditary spherocytosis type 4
+BMGC_DS21839,BMG_DS080485,episodic ataxia type 6
+BMGC_DS21840,BMG_DS080486,PHARC syndrome
+BMGC_DS21841,BMG_DS080487,hereditary spherocytosis type 5
+BMGC_DS21842,BMG_DS080488,primary autosomal recessive microcephaly 7
+BMGC_DS21843,BMG_DS080489,AGAT deficiency
+BMGC_DS21844,BMG_DS080490,leukocyte adhesion deficiency 3
+BMGC_DS21845,BMG_DS080491,autosomal dominant keratosis follicularis spinulosa decalvans
+BMGC_DS21846,BMG_DS080492,idiopathic generalized epilepsy 8
+BMGC_DS21847,BMG_DS080493,spastic quadriplegic cerebral palsy 2
+BMGC_DS21848,BMG_DS080494,hereditary spastic paraplegia 50
+BMGC_DS21849,BMG_DS080495,psoriasis 12
+BMGC_DS21850,BMG_DS080496,RNASET2-deficient cystic leukoencephalopathy
+BMGC_DS21851,BMG_DS080497,myofibrillar myopathy 6
+BMGC_DS21852,BMG_DS080498,multiple synostoses syndrome 3
+BMGC_DS21853,BMG_DS080499,"46,XY sex reversal 3"
+BMGC_DS21854,BMG_DS080500,autosomal dominant Emery-Dreifuss muscular dystrophy 4
+BMGC_DS21855,BMG_DS080501,primary biliary cholangitis 2
+BMGC_DS21856,BMG_DS080502,primary biliary cholangitis 3
+BMGC_DS21857,BMG_DS080503,combined or isolated pituitary hormone deficiency 1
+BMGC_DS21858,BMG_DS080504,idiopathic generalized epilepsy 10
+BMGC_DS21859,BMG_DS080505,atopic dermatitis 7
+BMGC_DS21860,BMG_DS080506,cerebral folate receptor alpha deficiency
+BMGC_DS21861,BMG_DS080507,autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5
+BMGC_DS21862,BMG_DS080508,primary congenital glaucoma
+BMGC_DS21863,BMG_DS080509,polycystic kidney disease 2
+BMGC_DS21864,BMG_DS080510,familial hemophagocytic lymphohistiocytosis 5
+BMGC_DS21865,BMG_DS080511,severe congenital neutropenia 2
+BMGC_DS21866,BMG_DS080512,hereditary sensory and autonomic neuropathy type 2B
+BMGC_DS21867,BMG_DS080513,congenital muscular dystrophy-dystroglycanopathy type A6
+BMGC_DS21868,BMG_DS080514,GABA aminotransferase deficiency
+BMGC_DS21869,BMG_DS080515,autosomal recessive intellectual developmental disorder 13
+BMGC_DS21870,BMG_DS080516,ankylosing spondylitis 3
+BMGC_DS21871,BMG_DS080517,hypertrophic cardiomyopathy 13
+BMGC_DS21872,BMG_DS080518,hypertrophic cardiomyopathy 14
+BMGC_DS21873,BMG_DS080519,Waardenburg syndrome type 4B
+BMGC_DS21874,BMG_DS080520,Waardenburg syndrome type 4C
+BMGC_DS21875,BMG_DS080521,hypermanganesemia with dystonia 1
+BMGC_DS21876,BMG_DS080522,spondylometaphyseal dysplasia Megarbane-Dagher-Melike type
+BMGC_DS21877,BMG_DS080523,rhabdoid tumor predisposition syndrome 2
+BMGC_DS21878,BMG_DS080524,maturity-onset diabetes of the young type 10
+BMGC_DS21879,BMG_DS080525,spinocerebellar ataxia type 30
+BMGC_DS21880,BMG_DS080526,maturity-onset diabetes of the young type 11
+BMGC_DS21881,BMG_DS080527,amyotrophic lateral sclerosis type 12
+BMGC_DS21882,BMG_DS080528,congenital disorder of glycosylation type IIj
+BMGC_DS21883,BMG_DS080529,common variable immunodeficiency 3
+BMGC_DS21884,BMG_DS080530,cytochrome P450 oxidoreductase deficiency
+BMGC_DS21885,BMG_DS080531,congenital disorder of glycosylation type IIi
+BMGC_DS21886,BMG_DS080532,fetal encasement syndrome
+BMGC_DS21887,BMG_DS080533,hereditary sensory and autonomic neuropathy type 1C
+BMGC_DS21888,BMG_DS080534,intellectual disability-severe speech delay-mild dysmorphism syndrome
+BMGC_DS21889,BMG_DS080535,age related macular degeneration 6
+BMGC_DS21890,BMG_DS080536,fatal infantile hypertonic myofibrillar myopathy
+BMGC_DS21891,BMG_DS080537,familial partial lipodystrophy type 4
+BMGC_DS21892,BMG_DS080538,schizophrenia 15
+BMGC_DS21893,BMG_DS080539,autosomal dominant intellectual developmental disorder 6
+BMGC_DS21894,BMG_DS080540,autosomal recessive dyskeratosis congenita 3
+BMGC_DS21895,BMG_DS080541,autosomal dominant dyskeratosis congenita 3
+BMGC_DS21896,BMG_DS080542,Nestor-Guillermo progeria syndrome
+BMGC_DS21897,BMG_DS080543,progressive myoclonus epilepsy 6
+BMGC_DS21898,BMG_DS080544,autosomal recessive intellectual developmental disorder 14
+BMGC_DS21899,BMG_DS080545,PSPH deficiency
+BMGC_DS21900,BMG_DS080546,psoriasis 13
+BMGC_DS21901,BMG_DS080547,chondrodysplasia with joint dislocations gPAPP type
+BMGC_DS21902,BMG_DS080548,multiple congenital anomalies-hypotonia-seizures syndrome 1
+BMGC_DS21903,BMG_DS080549,Fanconi anemia complementation group G
+BMGC_DS21904,BMG_DS080550,combined oxidative phosphorylation deficiency 8
+BMGC_DS21905,BMG_DS080551,autosomal dominant intellectual developmental disorder 7
+BMGC_DS21906,BMG_DS080552,autosomal dominant intellectual developmental disorder 2
+BMGC_DS21907,BMG_DS080553,mosaic variegated aneuploidy syndrome 2
+BMGC_DS21908,BMG_DS080554,hydrolethalus syndrome 2
+BMGC_DS21909,BMG_DS080555,spinocerebellar ataxia type 36
+BMGC_DS21910,BMG_DS080556,platelet-type bleeding disorder 14
+BMGC_DS21911,BMG_DS080557,autosomal recessive intellectual developmental disorder 16
+BMGC_DS21912,BMG_DS080558,autosomal recessive spinocerebellar ataxia 11
+BMGC_DS21913,BMG_DS080559,autosomal recessive intellectual developmental disorder 18
+BMGC_DS21914,BMG_DS080560,autosomal dominant intellectual developmental disorder 10
+BMGC_DS21915,BMG_DS080561,"46,XY sex reversal 8"
+BMGC_DS21916,BMG_DS080562,juvenile myoclonic epilepsy 9
+BMGC_DS21917,BMG_DS080563,autosomal dominant Wolfram syndrome
+BMGC_DS21918,BMG_DS080564,multiple mitochondrial dysfunctions syndrome 2
+BMGC_DS21919,BMG_DS080565,autosomal recessive intellectual developmental disorder 31
+BMGC_DS21920,BMG_DS080566,hereditary nonpolyposis colorectal cancer type 6
+BMGC_DS21921,BMG_DS080567,autosomal recessive intellectual developmental disorder 29
+BMGC_DS21922,BMG_DS080568,autosomal recessive intellectual developmental disorder 33
+BMGC_DS21923,BMG_DS080569,autosomal recessive intellectual developmental disorder 30
+BMGC_DS21924,BMG_DS080570,autosomal recessive intellectual developmental disorder 23
+BMGC_DS21925,BMG_DS080571,autosomal recessive intellectual developmental disorder 24
+BMGC_DS21926,BMG_DS080572,autosomal recessive intellectual developmental disorder 25
+BMGC_DS21927,BMG_DS080573,autosomal recessive intellectual developmental disorder 28
+BMGC_DS21928,BMG_DS080574,hereditary nonpolyposis colorectal cancer type 7
+BMGC_DS21929,BMG_DS080575,early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome
+BMGC_DS21930,BMG_DS080576,congenital disorder of glycosylation Ir
+BMGC_DS21931,BMG_DS080577,developmental and epileptic encephalopathy 13
+BMGC_DS21932,BMG_DS080578,infantile cerebellar-retinal degeneration
+BMGC_DS21933,BMG_DS080579,congenital disorder of glycosylation type IIl
+BMGC_DS21934,BMG_DS080580,combined oxidative phosphorylation deficiency 9
+BMGC_DS21935,BMG_DS080581,Cornelia de Lange syndrome 4
+BMGC_DS21936,BMG_DS080582,combined oxidative phosphorylation deficiency 10
+BMGC_DS21937,BMG_DS080583,Brown-Vialetto-Van Laere syndrome 2
+BMGC_DS21938,BMG_DS080584,congenital disorder of glycosylation type IIk
+BMGC_DS21939,BMG_DS080585,IMAGe syndrome
+BMGC_DS21940,BMG_DS080586,"3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome"
+BMGC_DS21941,BMG_DS080587,mitochondrial pyruvate carrier deficiency
+BMGC_DS21942,BMG_DS080588,Sotos syndrome 2
+BMGC_DS21943,BMG_DS080589,centronuclear myopathy 4
+BMGC_DS21944,BMG_DS080590,idiopathic generalized epilepsy 12
+BMGC_DS21945,BMG_DS080591,peroxisome biogenesis disorder 3A
+BMGC_DS21946,BMG_DS080592,peroxisome biogenesis disorder 4A
+BMGC_DS21947,BMG_DS080593,peroxisome biogenesis disorder 6A
+BMGC_DS21948,BMG_DS080594,Peroxisome biogenesis disorder 6B
+BMGC_DS21949,BMG_DS080595,Peroxisome biogenesis disorder 7B
+BMGC_DS21950,BMG_DS080596,peroxisome biogenesis disorder 8A
+BMGC_DS21951,BMG_DS080597,Peroxisome biogenesis disorder 8B
+BMGC_DS21952,BMG_DS080598,Peroxisome biogenesis disorder 9B
+BMGC_DS21953,BMG_DS080599,autosomal recessive distal hereditary motor neuronopathy 5
+BMGC_DS21954,BMG_DS080600,congenital disorder of glycosylation It
+BMGC_DS21955,BMG_DS080601,combined oxidative phosphorylation deficiency 11
+BMGC_DS21956,BMG_DS080602,combined oxidative phosphorylation deficiency 12
+BMGC_DS21957,BMG_DS080603,combined oxidative phosphorylation deficiency 13
+BMGC_DS21958,BMG_DS080604,combined oxidative phosphorylation deficiency 14
+BMGC_DS21959,BMG_DS080605,combined oxidative phosphorylation deficiency 15
+BMGC_DS21960,BMG_DS080606,developmental and epileptic encephalopathy 14
+BMGC_DS21961,BMG_DS080607,Schuurs-Hoeijmakers Syndrome
+BMGC_DS21962,BMG_DS080608,congenital disorder of glycosylation Iu
+BMGC_DS21963,BMG_DS080609,distal arthrogryposis type 5D
+BMGC_DS21964,BMG_DS080610,autosomal recessive intellectual developmental disorder 35
+BMGC_DS21965,BMG_DS080611,osteosclerotic metaphyseal dysplasia
+BMGC_DS21966,BMG_DS080612,schizophrenia 18
+BMGC_DS21967,BMG_DS080613,familial partial lipodystrophy type 5
+BMGC_DS21968,BMG_DS080614,"neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies"
+BMGC_DS21969,BMG_DS080615,spinal muscular atrophy with lower extremity predominant 2A
+BMGC_DS21970,BMG_DS080616,oculocutaneous albinism type V
+BMGC_DS21971,BMG_DS080617,multiple mitochondrial dysfunctions syndrome 3
+BMGC_DS21972,BMG_DS080618,central precocious puberty 2
+BMGC_DS21973,BMG_DS080619,autosomal recessive spinocerebellar ataxia 14
+BMGC_DS21974,BMG_DS080620,coronin-1A deficiency
+BMGC_DS21975,BMG_DS080621,mitochondrial DNA depletion syndrome 13
+BMGC_DS21976,BMG_DS080622,Bainbridge-Ropers syndrome
+BMGC_DS21977,BMG_DS080623,autosomal recessive intellectual developmental disorder 37
+BMGC_DS21978,BMG_DS080624,autosomal dominant intellectual developmental disorder 21
+BMGC_DS21979,BMG_DS080625,"alacrima, achalasia, and impaired intellectual development syndrome"
+BMGC_DS21980,BMG_DS080626,familial hypobetalipoproteinemia 1
+BMGC_DS21981,BMG_DS080627,autosomal dominant distal hereditary motor neuronopathy 6
+BMGC_DS21982,BMG_DS080628,congenital disorder of glycosylation Ix
+BMGC_DS21983,BMG_DS080629,autosomal recessive intellectual developmental disorder 41
+BMGC_DS21984,BMG_DS080630,autosomal recessive spinocerebellar ataxia 15
+BMGC_DS21985,BMG_DS080631,Bosch-Boonstra-Schaaf optic atrophy syndrome
+BMGC_DS21986,BMG_DS080632,developmental and epileptic encephalopathy 19
+BMGC_DS21987,BMG_DS080633,autosomal dominant intellectual developmental disorder 23
+BMGC_DS21988,BMG_DS080634,common variable immunodeficiency 11
+BMGC_DS21989,BMG_DS080635,autosomal recessive spinocerebellar ataxia 16
+BMGC_DS21990,BMG_DS080636,pontocerebellar hypoplasia type 10
+BMGC_DS21991,BMG_DS080637,autosomal recessive intellectual developmental disorder 43
+BMGC_DS21992,BMG_DS080638,autosomal dominant intellectual developmental disorder 26
+BMGC_DS21993,BMG_DS080639,Culler-Jones syndrome
+BMGC_DS21994,BMG_DS080640,Helsmoortel-Van Der Aa Syndrome
+BMGC_DS21995,BMG_DS080641,progressive familial intrahepatic cholestasis 4
+BMGC_DS21996,BMG_DS080642,Tatton-Brown-Rahman syndrome
+BMGC_DS21997,BMG_DS080643,orofacial cleft 14
+BMGC_DS21998,BMG_DS080644,developmental and epileptic encephalopathy 25
+BMGC_DS21999,BMG_DS080645,combined oxidative phosphorylation deficiency 21
+BMGC_DS22000,BMG_DS080646,autosomal recessive intellectual developmental disorder 44
+BMGC_DS22001,BMG_DS080647,orofaciodigital syndrome XIV
+BMGC_DS22002,BMG_DS080648,spinocerebellar ataxia type 38
+BMGC_DS22003,BMG_DS080649,autosomal recessive intellectual developmental disorder 45
+BMGC_DS22004,BMG_DS080650,familial partial lipodystrophy type 6
+BMGC_DS22005,BMG_DS080651,severe congenital neutropenia 6
+BMGC_DS22006,BMG_DS080652,spinocerebellar ataxia type 40
+BMGC_DS22007,BMG_DS080653,episodic ataxia type 8
+BMGC_DS22008,BMG_DS080654,developmental and epileptic encephalopathy 26
+BMGC_DS22009,BMG_DS080655,autosomal dominant intellectual developmental disorder 29
+BMGC_DS22010,BMG_DS080656,muscular dystrophy-dystroglycanopathy type C12
+BMGC_DS22011,BMG_DS080657,psoriasis 15
+BMGC_DS22012,BMG_DS080658,autosomal recessive intellectual developmental disorder 46
+BMGC_DS22013,BMG_DS080659,autosomal recessive spinocerebellar ataxia 17
+BMGC_DS22014,BMG_DS080660,rhizomelic chondrodysplasia punctate type 4
+BMGC_DS22015,BMG_DS080661,combined oxidative phosphorylation deficiency 23
+BMGC_DS22016,BMG_DS080662,Ruijs-Aalfs syndrome
+BMGC_DS22017,BMG_DS080663,chronic atrial and intestinal dysrhythmia
+BMGC_DS22018,BMG_DS080664,isolated mitochondrial myopathy
+BMGC_DS22019,BMG_DS080665,lissencephaly 6
+BMGC_DS22020,BMG_DS080666,progressive myoclonus epilepsy 8
+BMGC_DS22021,BMG_DS080667,combined oxidative phosphorylation deficiency 24
+BMGC_DS22022,BMG_DS080668,congenital limbs-face contractures-hypotonia-developmental delay syndrome
+BMGC_DS22023,BMG_DS080669,Arboleda-Tham syndrome
+BMGC_DS22024,BMG_DS080670,autosomal recessive intellectual developmental disorder 48
+BMGC_DS22025,BMG_DS080671,primary coenzyme Q10 deficiency 7
+BMGC_DS22026,BMG_DS080672,congenital bile acid synthesis defect 5
+BMGC_DS22027,BMG_DS080673,autosomal recessive spinocerebellar ataxia 19
+BMGC_DS22028,BMG_DS080674,autosomal dominant intellectual developmental disorder 33
+BMGC_DS22029,BMG_DS080675,developmental and epileptic encephalopathy 31A
+BMGC_DS22030,BMG_DS080676,autosomal dominant intellectual developmental disorder 34
+BMGC_DS22031,BMG_DS080677,autosomal recessive spinocerebellar ataxia 20
+BMGC_DS22032,BMG_DS080678,autosomal dominant intellectual developmental disorder 36
+BMGC_DS22033,BMG_DS080679,White-Sutton syndrome
+BMGC_DS22034,BMG_DS080680,developmental and epileptic encephalopathy 32
+BMGC_DS22035,BMG_DS080681,mandibulofacial dysostosis with alopecia
+BMGC_DS22036,BMG_DS080682,multiple mitochondrial dysfunctions syndrome 4
+BMGC_DS22037,BMG_DS080683,autosomal dominant intellectual developmental disorder 38
+BMGC_DS22038,BMG_DS080684,cerebellar ataxia type 41
+BMGC_DS22039,BMG_DS080685,"autoimmune interstitial lung, joint, and kidney disease"
+BMGC_DS22040,BMG_DS080686,hypomyelinating leukodystrophy 10
+BMGC_DS22041,BMG_DS080687,myoclonic-atonic epilepsy
+BMGC_DS22042,BMG_DS080688,combined oxidative phosphorylation deficiency 25
+BMGC_DS22043,BMG_DS080689,hereditary spastic paraplegia 74
+BMGC_DS22044,BMG_DS080690,developmental and epileptic encephalopathy 50
+BMGC_DS22045,BMG_DS080691,autosomal recessive intellectual developmental disorder 50
+BMGC_DS22046,BMG_DS080692,hereditary sensory and autonomic neuropathy type 8
+BMGC_DS22047,BMG_DS080693,Charcot-Marie-Tooth disease axonal type 2V
+BMGC_DS22048,BMG_DS080694,cone-rod dystrophy 21
+BMGC_DS22049,BMG_DS080695,autosomal recessive Emery-Dreifuss muscular dystrophy 3
+BMGC_DS22050,BMG_DS080696,combined oxidative phosphorylation deficiency 26
+BMGC_DS22051,BMG_DS080697,progressive myoclonus epilepsy 9
+BMGC_DS22052,BMG_DS080698,Klippel-Feil syndrome 4
+BMGC_DS22053,BMG_DS080699,spondyloepiphyseal dysplasia Stanescu type
+BMGC_DS22054,BMG_DS080700,immunodeficiency 42
+BMGC_DS22055,BMG_DS080701,"Charcot-Marie-Tooth disease, axonal type 2W"
+BMGC_DS22056,BMG_DS080702,developmental and epileptic encephalopathy 35
+BMGC_DS22057,BMG_DS080703,Charcot-Marie-Tooth disease axonal type 2X
+BMGC_DS22058,BMG_DS080704,combined oxidative phosphorylation deficiency 27
+BMGC_DS22059,BMG_DS080705,idiopathic generalized epilepsy 14
+BMGC_DS22060,BMG_DS080706,Charcot-Marie-Tooth disease axonal type 2Z
+BMGC_DS22061,BMG_DS080707,rhizomelic chondrodysplasia punctata type 5
+BMGC_DS22062,BMG_DS080708,congenital disorder of glycosylation type IIn
+BMGC_DS22063,BMG_DS080709,congenital symmetric circumferential skin creases 2
+BMGC_DS22064,BMG_DS080710,orofacial cleft 15
+BMGC_DS22065,BMG_DS080711,combined oxidative phosphorylation deficiency 28
+BMGC_DS22066,BMG_DS080712,cerebellar ataxia type 42
+BMGC_DS22067,BMG_DS080713,combined oxidative phosphorylation deficiency 29
+BMGC_DS22068,BMG_DS080714,autosomal recessive limb-girdle muscular dystrophy type 2X
+BMGC_DS22069,BMG_DS080715,autosomal recessive limb-girdle muscular dystrophy type 2W
+BMGC_DS22070,BMG_DS080716,congenital disorder of glycosylation type IIo
+BMGC_DS22071,BMG_DS080717,congenital disorder of glycosylation type IIp
+BMGC_DS22072,BMG_DS080718,TANGO2-related metabolic encephalopathy and arrythmias
+BMGC_DS22073,BMG_DS080719,diphthamide deficiency syndrome 1
+BMGC_DS22074,BMG_DS080720,poor metabolism of thiopurines 2
+BMGC_DS22075,BMG_DS080721,hereditary spastic paraplegia 76
+BMGC_DS22076,BMG_DS080722,autosomal recessive spinocerebellar ataxia 23
+BMGC_DS22077,BMG_DS080723,autosomal dominant intellectual developmental disorder 42
+BMGC_DS22078,BMG_DS080724,combined oxidative phosphorylation deficiency 30
+BMGC_DS22079,BMG_DS080725,autosomal dominant intellectual developmental disorder 43
+BMGC_DS22080,BMG_DS080726,hypermanganesemia with dystonia 2
+BMGC_DS22081,BMG_DS080727,otulipenia
+BMGC_DS22082,BMG_DS080728,developmental and epileptic encephalopathy 42
+BMGC_DS22083,BMG_DS080729,patterned macular dystrophy 3
+BMGC_DS22084,BMG_DS080730,developmental and epileptic encephalopathy 46
+BMGC_DS22085,BMG_DS080731,intellectual developmental disorder with cardiac arrhythmia
+BMGC_DS22086,BMG_DS080732,Harel-Yoon syndrome
+BMGC_DS22087,BMG_DS080733,autosomal recessive intellectual developmental disorder 57
+BMGC_DS22088,BMG_DS080734,early onset progressive encephalopathy with brain atrophy and thin corpus callosum
+BMGC_DS22089,BMG_DS080735,hereditary spastic paraplegia 78
+BMGC_DS22090,BMG_DS080736,autosomal recessive limb-girdle muscular dystrophy type 2Z
+BMGC_DS22091,BMG_DS080737,autosomal recessive intellectual developmental disorder 58
+BMGC_DS22092,BMG_DS080738,childhood-onset dystonia with optic atrophy and basal ganglia abnormalities
+BMGC_DS22093,BMG_DS080739,amelogenesis imperfecta type 1J
+BMGC_DS22094,BMG_DS080740,anterior segment dysgenesis 8
+BMGC_DS22095,BMG_DS080741,autosomal recessive intellectual developmental disorder 59
+BMGC_DS22096,BMG_DS080742,congenital disorder of glycosylation type IIq
+BMGC_DS22097,BMG_DS080743,autosomal recessive intellectual developmental disorder 60
+BMGC_DS22098,BMG_DS080744,"46,XX sex reversal 4"
+BMGC_DS22099,BMG_DS080745,pituitary adenoma 5
+BMGC_DS22100,BMG_DS080746,spastic ataxia 8
+BMGC_DS22101,BMG_DS080747,autosomal recessive congenital ichthyosis 14
+BMGC_DS22102,BMG_DS080748,autosomal recessive congenital ichthyosis 13
+BMGC_DS22103,BMG_DS080749,autosomal dominant intellectual developmental disorder 45
+BMGC_DS22104,BMG_DS080750,autosomal dominant intellectual developmental disorder 46
+BMGC_DS22105,BMG_DS080751,multiple mitochondrial dysfunctions syndrome 5
+BMGC_DS22106,BMG_DS080752,schizophrenia 19
+BMGC_DS22107,BMG_DS080753,autosomal dominant intellectual developmental disorder 47
+BMGC_DS22108,BMG_DS080754,pituitary adenoma 3
+BMGC_DS22109,BMG_DS080755,pontocerebellar hypoplasia type 11
+BMGC_DS22110,BMG_DS080756,3-methylglutaconic aciduria type 9
+BMGC_DS22111,BMG_DS080757,combined oxidative phosphorylation deficiency 33
+BMGC_DS22112,BMG_DS080758,multiple epiphyseal dysplasia 7
+BMGC_DS22113,BMG_DS080759,autosomal dominant intellectual developmental disorder 48
+BMGC_DS22114,BMG_DS080760,spinocerebellar ataxia 45
+BMGC_DS22115,BMG_DS080761,spinocerebellar ataxia 46
+BMGC_DS22116,BMG_DS080762,autosomal recessive intellectual developmental disorder 61
+BMGC_DS22117,BMG_DS080763,autosomal dominant intellectual developmental disorder 50
+BMGC_DS22118,BMG_DS080764,autosomal dominant intellectual developmental disorder 51
+BMGC_DS22119,BMG_DS080765,autosomal dominant intellectual developmental disorder 52
+BMGC_DS22120,BMG_DS080766,autosomal dominant intellectual developmental disorder 53
+BMGC_DS22121,BMG_DS080767,autosomal dominant intellectual developmental disorder 54
+BMGC_DS22122,BMG_DS080768,geleophysic dysplasia 3
+BMGC_DS22123,BMG_DS080769,immunodeficiency 55
+BMGC_DS22124,BMG_DS080770,amyotrophic lateral sclerosis type 23
+BMGC_DS22125,BMG_DS080771,autosomal dominant intellectual developmental disorder 56
+BMGC_DS22126,BMG_DS080772,combined oxidative phosphorylation deficiency 34
+BMGC_DS22127,BMG_DS080773,amyotrophic lateral sclerosis type 24
+BMGC_DS22128,BMG_DS080774,amyotrophic lateral sclerosis type 25
+BMGC_DS22129,BMG_DS080775,juvenile myoclonic epilepsy 10
+BMGC_DS22130,BMG_DS080776,orofaciodigital syndrome XVIII
+BMGC_DS22131,BMG_DS080777,multiple mitochondrial dysfunctions syndrome 6
+BMGC_DS22132,BMG_DS080778,Ehlers-Danlos syndrome classic-like 2
+BMGC_DS22133,BMG_DS080779,autosomal recessive intellectual developmental disorder 63
+BMGC_DS22134,BMG_DS080780,autosomal recessive intellectual developmental disorder 64
+BMGC_DS22135,BMG_DS080781,autosomal recessive intellectual developmental disorder 65
+BMGC_DS22136,BMG_DS080782,developmental and epileptic encephalopathy 71
+BMGC_DS22137,BMG_DS080783,idiopathic generalized epilepsy 15
+BMGC_DS22138,BMG_DS080784,developmental and epileptic encephalopathy 73
+BMGC_DS22139,BMG_DS080785,spondyloepimetaphyseal dysplasia with joint laxity type 3
+BMGC_DS22140,BMG_DS080786,combined oxidative phosphorylation deficiency 39
+BMGC_DS22141,BMG_DS080787,congenital myopathy 14
+BMGC_DS22142,BMG_DS080788,long QT syndrome 8
+BMGC_DS22143,BMG_DS080789,congenital nongoitrous hypothyroidism 7
+BMGC_DS22144,BMG_DS080790,spondyloepiphyseal dysplasia Nishimura type
+BMGC_DS22145,BMG_DS080791,primary ciliary dyskinesia 42
+BMGC_DS22146,BMG_DS080792,congenital megabladder
+BMGC_DS22147,BMG_DS080793,combined oxidative phosphorylation deficiency 40
+BMGC_DS22148,BMG_DS080794,galactosemia 4
+BMGC_DS22149,BMG_DS080795,oculopharyngodistal myopathy 2
+BMGC_DS22150,BMG_DS080796,spondylometaphyseal dysplasia with corneal dystrophy
+BMGC_DS22151,BMG_DS080797,AMED syndrome
+BMGC_DS22152,BMG_DS080798,Mahvash Disease
+BMGC_DS22153,BMG_DS080799,autosomal recessive intellectual developmental disorder 73
+BMGC_DS22154,BMG_DS080800,autosomal recessive intellectual developmental disorder 76
+BMGC_DS22155,BMG_DS080801,autosomal recessive intellectual developmental disorder 77
+BMGC_DS22156,BMG_DS080802,developmental and epileptic encephalopathy 107
+BMGC_DS22157,BMG_DS080803,hereditary spastic paraplegia 70
+BMGC_DS22158,BMG_DS080804,nevoid basal cell carcinoma syndrome 2
+BMGC_DS22159,BMG_DS080805,bradyopsia 2
+BMGC_DS22160,BMG_DS080806,epidermolytic palmoplantar keratoderma 2
+BMGC_DS22161,BMG_DS080807,spermatogenic failure 95
+BMGC_DS22162,BMG_DS080808,congenital dyserythropoietic anemia type IVb
+BMGC_DS22163,BMG_DS080809,primary cutaneous amyloidosis
+BMGC_DS22164,BMG_DS080810,intracranial berry aneurysm
+BMGC_DS22165,BMG_DS080811,distal arthrogryposis
+BMGC_DS22166,BMG_DS080812,Stickler syndrome
+BMGC_DS22167,BMG_DS080813,cerebral cavernous malformation
+BMGC_DS22168,BMG_DS080814,orofacial cleft
+BMGC_DS22169,BMG_DS080815,familial febrile seizures
+BMGC_DS22170,BMG_DS080816,craniometaphyseal dysplasia
+BMGC_DS22171,BMG_DS080817,Kenny-Caffey syndrome
+BMGC_DS22172,BMG_DS080818,retinal macular dystrophy
+BMGC_DS22173,BMG_DS080819,Teebi hypertelorism syndrome
+BMGC_DS22174,BMG_DS080820,hyper IgE syndrome
+BMGC_DS22175,BMG_DS080821,LADD syndrome
+BMGC_DS22176,BMG_DS080822,autosomal dominant intellectual developmental disorder
+BMGC_DS22177,BMG_DS080823,multiple benign circumferential skin creases on limbs
+BMGC_DS22178,BMG_DS080824,spinal muscular atrophy with lower extremity predominant
+BMGC_DS22179,BMG_DS080825,nonsyndromic congenital nail disorder
+BMGC_DS22180,BMG_DS080826,oculopharyngodistal myopathy
+BMGC_DS22181,BMG_DS080827,polycystic kidney disease
+BMGC_DS22182,BMG_DS080828,brain small vessel disease
+BMGC_DS22183,BMG_DS080829,progeroid syndrome
+BMGC_DS22184,BMG_DS080830,autosomal dominant distal hereditary motor neuronopathy
+BMGC_DS22185,BMG_DS080831,proximal symphalangism
+BMGC_DS22186,BMG_DS080832,multiple synostoses syndrome
+BMGC_DS22187,BMG_DS080833,familial glucocorticoid deficiency
+BMGC_DS22188,BMG_DS080834,alopecia-mental retardation syndrome
+BMGC_DS22189,BMG_DS080835,ARC syndrome
+BMGC_DS22190,BMG_DS080836,3-methylcrotonyl-CoA carboxylase deficiency
+BMGC_DS22191,BMG_DS080837,congenital disorder of glycosylation type I
+BMGC_DS22192,BMG_DS080838,autosomal recessive cerebellar ataxia
+BMGC_DS22193,BMG_DS080839,"craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome"
+BMGC_DS22194,BMG_DS080840,peroxisomal biogenesis disorder
+BMGC_DS22195,BMG_DS080841,cerebrooculofacioskeletal syndrome
+BMGC_DS22196,BMG_DS080842,congenital diarrhea
+BMGC_DS22197,BMG_DS080843,congenital muscular dystrophy-dystroglycanopathy type A
+BMGC_DS22198,BMG_DS080844,benign recurrent intrahepatic cholestasis
+BMGC_DS22199,BMG_DS080845,Baraitser-Winter syndrome
+BMGC_DS22200,BMG_DS080846,mandibuloacral dysplasia
+BMGC_DS22201,BMG_DS080847,autosomal recessive intellectual developmental disorder
+BMGC_DS22202,BMG_DS080848,primary autosomal recessive microcephaly
+BMGC_DS22203,BMG_DS080849,nuclear type mitochondrial complex I deficiency
+BMGC_DS22204,BMG_DS080850,proteosome-associated autoinflammatory syndrome
+BMGC_DS22205,BMG_DS080851,spermatogenic failure
+BMGC_DS22206,BMG_DS080852,pancreatic agenesis
+BMGC_DS22207,BMG_DS080853,congenital bilateral absence of vas deferens
+BMGC_DS22208,BMG_DS080854,spondylocostal dysostosis
+BMGC_DS22209,BMG_DS080855,ectodermal dysplasia and immune deficiency
+BMGC_DS22210,BMG_DS080856,cerebral creatine deficiency syndrome
+BMGC_DS22211,BMG_DS080857,lymphoproliferative syndrome
+BMGC_DS22212,BMG_DS080858,developmental and epileptic encephalopathy
+BMGC_DS22213,BMG_DS080859,syndromic X-linked intellectual disability
+BMGC_DS22214,BMG_DS080860,syndromic microphthalmia
+BMGC_DS22215,BMG_DS080861,MLS syndrome
+BMGC_DS22216,BMG_DS080862,hypomyelinating leukodystrophy
+BMGC_DS22217,BMG_DS080863,Y-linked deafness
+BMGC_DS22218,BMG_DS080864,D-2-hydroxyglutaric aciduria
+BMGC_DS22219,BMG_DS080865,benign familial infantile epilepsy
+BMGC_DS22220,BMG_DS080866,mitochondrial DNA depletion syndrome
+BMGC_DS22221,BMG_DS080867,autosomal recessive distal hereditary motor neuronopathy
+BMGC_DS22222,BMG_DS080868,advanced sleep phase syndrome
+BMGC_DS22223,BMG_DS080869,familial focal epilepsy with variable foci
+BMGC_DS22224,BMG_DS080870,coenzyme Q10 deficiency disease
+BMGC_DS22225,BMG_DS080871,congenital generalized lipodystrophy
+BMGC_DS22226,BMG_DS080872,combined oxidative phosphorylation deficiency
+BMGC_DS22227,BMG_DS080873,Kleefstra syndrome
+BMGC_DS22228,BMG_DS080874,hypophosphatemic nephrolithiasis/osteoporosis
+BMGC_DS22229,BMG_DS080875,muscular dystrophy-dystroglycanopathy type B
+BMGC_DS22230,BMG_DS080876,hypermanganesemia with dystonia
+BMGC_DS22231,BMG_DS080877,hot water epilepsy
+BMGC_DS22232,BMG_DS080878,complex cortical dysplasia with other brain malformations
+BMGC_DS22233,BMG_DS080879,multiple congenital anomalies-hypotonia-seizures syndrome
+BMGC_DS22234,BMG_DS080880,familial episodic pain syndrome
+BMGC_DS22235,BMG_DS080881,infantile liver failure syndrome
+BMGC_DS22236,BMG_DS080882,diphthamide deficiency syndrome
+BMGC_DS22237,BMG_DS080883,arthrogryposis multiplex congenita
+BMGC_DS22238,BMG_DS080884,Bryant-Li-Bhoj neurodevelopmental syndrome
+BMGC_DS22239,BMG_DS080904,"Botulism, unspecified"
+BMGC_DS22240,BMG_DS080952,
+BMGC_DS22241,BMG_DS080976,
+BMGC_DS22242,BMG_DS080978,
+BMGC_DS22243,BMG_DS081114,HIV disease clinical stage 1 without mention of tuberculosis or malaria
+BMGC_DS22244,BMG_DS081117,
+BMGC_DS22245,BMG_DS081174,
+BMGC_DS22246,BMG_DS081227,Streptococcus pneumoniae
+BMGC_DS22247,BMG_DS081342,Hepatocellular carcinoma of liver
+BMGC_DS22248,BMG_DS081907,
+BMGC_DS22249,BMG_DS081908,
+BMGC_DS22250,BMG_DS081909,
+BMGC_DS22251,BMG_DS081910,
+BMGC_DS22252,BMG_DS081911,
+BMGC_DS22253,BMG_DS081912,
+BMGC_DS22254,BMG_DS081913,
+BMGC_DS22255,BMG_DS081914,
+BMGC_DS22256,BMG_DS081916,
+BMGC_DS22257,BMG_DS081917,
+BMGC_DS22258,BMG_DS081918,
+BMGC_DS22259,BMG_DS081919,
+BMGC_DS22260,BMG_DS081920,
+BMGC_DS22261,BMG_DS081921,
+BMGC_DS22262,BMG_DS081922,
+BMGC_DS22263,BMG_DS081923,
+BMGC_DS22264,BMG_DS081924,
+BMGC_DS22265,BMG_DS081925,
+BMGC_DS22266,BMG_DS081926,
+BMGC_DS22267,BMG_DS081927,
+BMGC_DS22268,BMG_DS081928,
+BMGC_DS22269,BMG_DS081929,
+BMGC_DS22270,BMG_DS081930,
+BMGC_DS22271,BMG_DS081931,
+BMGC_DS22272,BMG_DS081932,
+BMGC_DS22273,BMG_DS081933,
+BMGC_DS22274,BMG_DS081934,
+BMGC_DS22275,BMG_DS081935,
+BMGC_DS22276,BMG_DS081936,
+BMGC_DS22277,BMG_DS081937,
+BMGC_DS22278,BMG_DS081938,
+BMGC_DS22279,BMG_DS081949,
+BMGC_DS22280,BMG_DS081950,
+BMGC_DS22281,BMG_DS081951,
+BMGC_DS22282,BMG_DS081952,
+BMGC_DS22283,BMG_DS081953,
+BMGC_DS22284,BMG_DS081954,
+BMGC_DS22285,BMG_DS081955,
+BMGC_DS22286,BMG_DS081956,
+BMGC_DS22287,BMG_DS081957,
+BMGC_DS22288,BMG_DS081958,
+BMGC_DS22289,BMG_DS081972,transient myeloproliferative syndrome
+BMGC_DS22290,BMG_DS081973,lymphoproliferative syndrome 2 | lymphoproliferative syndrome 1 | autoimmune lymphoproliferative syndrome type 2B
+BMGC_DS22291,BMG_DS081974,
+BMGC_DS22292,BMG_DS081975,
+BMGC_DS22293,BMG_DS081976,
+BMGC_DS22294,BMG_DS081977,
+BMGC_DS22295,BMG_DS081978,
+BMGC_DS22296,BMG_DS081979,
+BMGC_DS22297,BMG_DS081980,
+BMGC_DS22298,BMG_DS081981,
+BMGC_DS22299,BMG_DS081982,
+BMGC_DS22300,BMG_DS082038,Other specified inherited qualitative platelet defects
+BMGC_DS22301,BMG_DS082039,Hyperimmunoglobulin E syndromes
+BMGC_DS22302,BMG_DS082082,maturity-onset diabetes of the young
+BMGC_DS22303,BMG_DS082121,ectopic Cushing syndrome
+BMGC_DS22304,BMG_DS082136,aromatase excess syndrome
+BMGC_DS22305,BMG_DS082179,"Obesity, unspecified"
+BMGC_DS22306,BMG_DS082187,D-bifunctional protein deficiency | carnitine palmitoyltransferase I deficiency
+BMGC_DS22307,BMG_DS082189,hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | glycine N-methyltransferase deficiency | hypermethioninemia due to adenosine kinase deficiency
+BMGC_DS22308,BMG_DS082197,glycogen storage disease IXd | glycogen storage disease IXa
+BMGC_DS22309,BMG_DS082198,lethal congenital glycogen storage disease of heart
+BMGC_DS22310,BMG_DS082204,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,Scheie syndrome
+BMGC_DS22312,BMG_DS082211,autosomal recessive hypercholesterolemia
+BMGC_DS22313,BMG_DS082223,hemochromatosis type 1 | African iron overload | hemochromatosis type 5
+BMGC_DS22314,BMG_DS082225,renal hypomagnesemia 2 | renal hypomagnesemia 4 | intestinal hypomagnesemia 1 | primary hypomagnesemia | renal hypomagnesemia 3 | renal hypomagnesemia 6
+BMGC_DS22315,BMG_DS082226,familial hypocalciuric hypercalcemia 3 | familial hypocalciuric hypercalcemia 2 | familial hypocalciuric hypercalcemia | familial hypocalciuric hypercalcemia 1
+BMGC_DS22316,BMG_DS082230,TNF receptor–associated periodic syndrome | CINCA Syndrome
+BMGC_DS22317,BMG_DS082251,CADASIL 1 | CADASIL 2
+BMGC_DS22318,BMG_DS082273,Mild neurocognitive disorder
+BMGC_DS22319,BMG_DS082454,Post traumatic stress disorder
+BMGC_DS22320,BMG_DS082479,"Anorexia Nervosa, unspecified"
+BMGC_DS22321,BMG_DS082556,X-linked intellectual disability-psychosis-macroorchidism syndrome
+BMGC_DS22322,BMG_DS082559,syndromic X-linked intellectual disability 94
+BMGC_DS22323,BMG_DS082590,Rett syndrome
+BMGC_DS22324,BMG_DS082646,Huntington's disease-like 2 | Huntington's disease-like 1
+BMGC_DS22325,BMG_DS082648,hypomyelinating leukodystrophy 11 | hypomyelinating leukodystrophy 8 | hypomyelinating leukodystrophy 7
+BMGC_DS22326,BMG_DS082650,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,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,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,hypomyelinating leukodystrophy 5
+BMGC_DS22330,BMG_DS082707,"Transient ischaemic attack, unspecified"
+BMGC_DS22331,BMG_DS082765,
+BMGC_DS22332,BMG_DS082768,
+BMGC_DS22333,BMG_DS082773,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,Schwartz-Jampel syndrome 1
+BMGC_DS22335,BMG_DS082775,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,posterior polymorphous corneal dystrophy 2 | posterior polymorphous corneal dystrophy 1 | posterior polymorphous corneal dystrophy 3
+BMGC_DS22337,BMG_DS083025,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,
+BMGC_DS22339,BMG_DS083109,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,catecholaminergic polymorphic ventricular tachycardia 1
+BMGC_DS22341,BMG_DS083128,long QT syndrome 14 | long QT syndrome 1 | long QT syndrome 13 | long QT syndrome 15
+BMGC_DS22342,BMG_DS083134,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,BuddChiari syndrome
+BMGC_DS22344,BMG_DS083257,
+BMGC_DS22345,BMG_DS083312,Allergic asthma
+BMGC_DS22346,BMG_DS083314,Asthma
+BMGC_DS22347,BMG_DS083341,
+BMGC_DS22348,BMG_DS083347,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,"Columnar metaplastic epithelium of the oesophagus, unspecified"
+BMGC_DS22350,BMG_DS083412,
+BMGC_DS22351,BMG_DS083414,
+BMGC_DS22352,BMG_DS083456,
+BMGC_DS22353,BMG_DS083458,
+BMGC_DS22354,BMG_DS083461,
+BMGC_DS22355,BMG_DS083462,
+BMGC_DS22356,BMG_DS083465,
+BMGC_DS22357,BMG_DS083468,
+BMGC_DS22358,BMG_DS083471,
+BMGC_DS22359,BMG_DS083472,
+BMGC_DS22360,BMG_DS083474,
+BMGC_DS22361,BMG_DS083476,
+BMGC_DS22362,BMG_DS083478,
+BMGC_DS22363,BMG_DS083483,
+BMGC_DS22364,BMG_DS083498,"Diseases of the digestive system, unspecified"
+BMGC_DS22365,BMG_DS083593,
+BMGC_DS22366,BMG_DS083619,chromium allergic contact dermatitis | nickel allergic contact dermatitis
+BMGC_DS22367,BMG_DS083657,Palmoplantar pustulosis
+BMGC_DS22368,BMG_DS083658,Guttate psoriasis
+BMGC_DS22369,BMG_DS083669,familial cold autoinflammatory syndrome 4 | familial cold autoinflammatory syndrome | familial cold autoinflammatory syndrome 3 | familial cold autoinflammatory syndrome 1
+BMGC_DS22370,BMG_DS083779,
+BMGC_DS22371,BMG_DS083796,
+BMGC_DS22372,BMG_DS083807,
+BMGC_DS22373,BMG_DS083808,
+BMGC_DS22374,BMG_DS083812,Juvenile psoriatic arthritis
+BMGC_DS22375,BMG_DS083813,
+BMGC_DS22376,BMG_DS083831,
+BMGC_DS22377,BMG_DS083857,Bruck syndrome
+BMGC_DS22378,BMG_DS083897,Libman-Sacks endocarditis
+BMGC_DS22379,BMG_DS083903,Undifferentiated nonorgan specific systemic autoimmune disease
+BMGC_DS22380,BMG_DS083993,
+BMGC_DS22381,BMG_DS084120,
+BMGC_DS22382,BMG_DS084122,
+BMGC_DS22383,BMG_DS084124,
+BMGC_DS22384,BMG_DS084185,"Neuromuscular dysfunction of bladder, not elsewhere classified"
+BMGC_DS22385,BMG_DS084239,
+BMGC_DS22386,BMG_DS084242,
+BMGC_DS22387,BMG_DS084243,
+BMGC_DS22388,BMG_DS084465,pemphigus gestationis
+BMGC_DS22389,BMG_DS085000,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,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,cornea plana
+BMGC_DS22392,BMG_DS085049,Axenfeld-Rieger syndrome type 1 | Axenfeld-Rieger syndrome type 2 | anterior segment dysgenesis | Axenfeld-Rieger syndrome type 3
+BMGC_DS22393,BMG_DS085052,X-linked juvenile retinoschisis 1
+BMGC_DS22394,BMG_DS085087,multiple types of congenital heart defects 6 | dextro-looped transposition of the great arteries
+BMGC_DS22395,BMG_DS085090,right atrial isomerism
+BMGC_DS22396,BMG_DS085094,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,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,isolated cleft palate
+BMGC_DS22399,BMG_DS085233,Hirschsprung disease
+BMGC_DS22400,BMG_DS085243,Biliary atresia
+BMGC_DS22401,BMG_DS085264,hand-foot-genital syndrome
+BMGC_DS22402,BMG_DS085308,renal coloboma syndrome | oligomeganephronia
+BMGC_DS22403,BMG_DS085372,lethal congenital contracture syndrome
+BMGC_DS22404,BMG_DS085389,split hand-foot malformation 1
+BMGC_DS22405,BMG_DS085419,brachyolmia-amelogenesis imperfecta syndrome
+BMGC_DS22406,BMG_DS085420,spondylocarpotarsal synostosis syndrome
+BMGC_DS22407,BMG_DS085428,short-rib thoracic dysplasia 10 with or without polydactyly
+BMGC_DS22408,BMG_DS085429,autosomal dominant chondrodysplasia punctata | rhizomelic chondrodysplasia punctata type 1
+BMGC_DS22409,BMG_DS085432,progressive pseudorheumatoid arthropathy of childhood | Silverman-Handmaker type dyssegmental dysplasia
+BMGC_DS22410,BMG_DS085435,"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,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,autosomal recessive congenital ichthyosis 4B
+BMGC_DS22413,BMG_DS085455,epidermolysis bullosa simplex Dowling-Meara type | epidermolysis bullosa simplex Ogna type | epidermolysis bullosa simplex with muscular dystrophy
+BMGC_DS22414,BMG_DS085456,junctional epidermolysis bullosa Herlitz type
+BMGC_DS22415,BMG_DS085457,recessive dystrophic epidermolysis bullosa
+BMGC_DS22416,BMG_DS085458,junctional epidermolysis bullosa with pyloric atresia | junctional epidermolysis bullosa non-Herlitz type
+BMGC_DS22417,BMG_DS085460,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,Noonan syndrome 10 | Noonan syndrome 1 | Noonan syndrome 9 | Noonan syndrome 8 | Noonan syndrome 7 | Seckel syndrome
+BMGC_DS22419,BMG_DS085485,"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,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,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,Halitosis
+BMGC_DS22423,BMG_DS085718,"Elevated blood glucose level, unspecified"
+BMGC_DS22424,BMG_DS086495,"Unspecified injuries of spine or trunk, level unspecified"
+BMGC_DS22425,BMG_DS086961,Allergic or hypersensitivity conditions of unspecified type
+BMGC_DS22426,BMG_DS091971,Obesity
+BMGC_DS22427,BMG_DS094697,Cystic fibrosis
+BMGC_DS22428,BMG_DS095586,Psoriasis
+BMGC_DS22429,BMG_DS118713,