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<s>[INST] Is Ovarian Epithelial, Fallopian Tube, and Primary Peritoneal Cancer inherited ? [/INST] Some ovarian, fallopian tube, and primary peritoneal cancers are caused by inherited gene mutations (changes). The genes in cells carry the hereditary information that is received from a persons parents. Hereditary ovaria... |
<s>[INST] Is Neuroblastoma inherited ? [/INST] Neuroblastoma is sometimes caused by a gene mutation (change) passed from the parent to the child. Gene mutations that increase the risk of neuroblastoma are sometimes inherited (passed from the parent to the child). In children with a gene mutation, neuroblastoma usually ... |
<s>[INST] Is Retinoblastoma inherited ? [/INST] Retinoblastoma occurs in heritable and nonheritable forms.
A child is thought to have the heritable form of retinoblastoma when one of the following is true: - There is a family history of retinoblastoma. - There is a certain mutation (chang... |
<s>[INST] Is Male Breast Cancer inherited ? [/INST] Male breast cancer is sometimes caused by inherited gene mutations (changes).The genes in cells carry the hereditary information that is received from a persons parents. Hereditary breast cancer makes up about 5% to 10% of all breast cancer. Some mutated genes related... |
<s>[INST] Is Breast Cancer inherited ? [/INST] Breast cancer is sometimes caused by inherited gene mutations (changes). The genes in cells carry the hereditary information that is received from a persons parents. Hereditary breast cancer makes up about 5% to 10% of all breast cancer. Some mutated genes related to breas... |
<s>[INST] Is cyclic neutropenia inherited ? [/INST] Cyclic neutropenia is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In most cases, an affected person inherits the mutation from one affected parent. Other cases result from new ... |
<s>[INST] Is Behet disease inherited ? [/INST] Most cases of Behet disease are sporadic, which means they occur in people with no history of the disorder in their family. A small percentage of all cases have been reported to run in families; however, the condition does not have a clear pattern of inheritance. </s> |
<s>[INST] Is Nijmegen breakage syndrome inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do no... |
<s>[INST] Is congenital stromal corneal dystrophy inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. </s> |
<s>[INST] Is Beare-Stevenson cutis gyrata syndrome inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. All reported cases have resulted from new mutations in the gene, and occurred in people with no ... |
<s>[INST] Is porphyria inherited ? [/INST] Some types of porphyria are inherited in an autosomal dominant pattern, which means one copy of the gene in each cell is mutated. This single mutation is sufficient to reduce the activity of an enzyme needed for heme production, which increases the risk of developing signs and... |
<s>[INST] Is isodicentric chromosome 15 syndrome inherited ? [/INST] Isodicentric chromosome 15 syndrome is usually not inherited. The chromosomal change that causes the disorder typically occurs as a random event during the formation of reproductive cells (eggs or sperm) in a parent of the affected individual. Most af... |
<s>[INST] Is polymicrogyria inherited ? [/INST] Isolated polymicrogyria can have different inheritance patterns. Several forms of the condition, including bilateral frontoparietal polymicrogyria (which is associated with mutations in the ADGRG1 gene), have an autosomal recessive pattern of inheritance. In autosomal rec... |
<s>[INST] Is Pompe disease inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs ... |
<s>[INST] Is hereditary xanthinuria inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not sh... |
<s>[INST] Is hyperkalemic periodic paralysis inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. </s> |
<s>[INST] Is arginase deficiency inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show ... |
<s>[INST] Is neuroblastoma inherited ? [/INST] Most people with neuroblastoma have sporadic neuroblastoma, meaning the condition arose from somatic mutations in the body's cells and was not inherited. About 1 to 2 percent of affected individuals have familial neuroblastoma. This form of the condition has an autosomal ... |
<s>[INST] Is Birt-Hogg-Dub syndrome inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered FLCN gene in each cell is sufficient to cause the disorder. In most cases, an affected person inherits the mutation from one affected parent. Less commonly, the condi... |
<s>[INST] Is N-acetylglutamate synthase deficiency inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typi... |
<s>[INST] Is Winchester syndrome inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show ... |
<s>[INST] Is Wolman disease inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs... |
<s>[INST] Is purine nucleoside phosphorylase deficiency inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they... |
<s>[INST] Is Cushing disease inherited ? [/INST] Most cases of Cushing disease are sporadic, which means they occur in people with no history of the disorder in their family. Rarely, the condition has been reported to run in families; however, it does not have a clear pattern of inheritance. The various syndromes that... |
<s>[INST] Is pseudoxanthoma elasticum inherited ? [/INST] PXE is inherited in an autosomal recessive manner, which means both copies of the gene in each cell have mutations. Most often, the parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but do not show signs and ... |
<s>[INST] Is beta-mannosidosis inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show si... |
<s>[INST] Is spondylocostal dysostosis inherited ? [/INST] Spondylocostal dysostosis can have different inheritance patterns. Types 1, 2, 3, and 4 are inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive co... |
<s>[INST] Is biotinidase deficiency inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the BTD gene in each cell have mutations. The parents of an individual with biotinidase deficiency each carry one copy of the mutated gene, but they typically do not have any... |
<s>[INST] Is erythrokeratodermia variabilis et progressiva inherited ? [/INST] EKVP is most often inherited in an autosomal dominant pattern, which means one copy of an altered gene in each cell is sufficient to cause the disorder. In most cases, an affected person inherits the mutation from one affected parent. Other ... |
<s>[INST] Is pseudohypoaldosteronism type 1 inherited ? [/INST] PHA1 can have different inheritance patterns. When the condition is caused by mutations in the NR3C2 gene, it is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. When PHA... |
<s>[INST] Is trichothiodystrophy inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show ... |
<s>[INST] Is hemophilia inherited ? [/INST] Hemophilia A and hemophilia B are inherited in an X-linked recessive pattern. The genes associated with these conditions are located on the X chromosome, which is one of the two sex chromosomes. In males (who have only one X chromosome), one altered copy of the gene in each c... |
<s>[INST] Is gnathodiaphyseal dysplasia inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In some cases, an affected person inherits the mutation from one affected parent. Other cases result from ... |
<s>[INST] Is primary spontaneous pneumothorax inherited ? [/INST] When this condition is caused by mutations in the FLCN gene, it is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In most cases, a person inherits the FLCN gene mutat... |
<s>[INST] Is hereditary paraganglioma-pheochromocytoma inherited ? [/INST] Hereditary paraganglioma-pheochromocytoma is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to increase the risk of developing tumors. An additional mutation that deletes the norma... |
<s>[INST] Is arterial tortuosity syndrome inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do ... |
<s>[INST] Is deafness and myopia syndrome inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do ... |
<s>[INST] Is primary sclerosing cholangitis inherited ? [/INST] The inheritance pattern of primary sclerosing cholangitis is unknown because many genetic and environmental factors are likely to be involved. This condition tends to cluster in families, however, and having an affected family member is a risk factor for d... |
<s>[INST] Is succinyl-CoA:3-ketoacid CoA transferase deficiency inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, ... |
<s>[INST] Is dermatofibrosarcoma protuberans inherited ? [/INST] Dermatofibrosarcoma protuberans results from a new mutation that occurs in the body's cells after conception and is found only in the tumor cells. This type of genetic change is called a somatic mutation and is generally not inherited. </s> |
<s>[INST] Is Jervell and Lange-Nielsen syndrome inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. Most often, the parents of a child with an autosomal recessive disorder are not affected, but are carriers of one copy of th... |
<s>[INST] Is isolated Pierre Robin sequence inherited ? [/INST] Isolated Pierre Robin sequence is usually not inherited. It typically results from new genetic changes and occurs in people with no history of the disorder in their family. When the condition is inherited, it follows an autosomal dominant pattern, which me... |
<s>[INST] Is prolidase deficiency inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show... |
<s>[INST] Is Melnick-Needles syndrome inherited ? [/INST] This condition is inherited in an X-linked dominant pattern. The gene associated with this condition is located on the X chromosome, which is one of the two sex chromosomes. In females (who have two X chromosomes), a mutation in one of the two copies of the gene... |
<s>[INST] Is restless legs syndrome inherited ? [/INST] The inheritance pattern of restless legs syndrome is usually unclear because many genetic and environmental factors can be involved. The disorder often runs in families: 40 to 90 percent of affected individuals report having at least one affected first-degree rela... |
<s>[INST] Is inclusion body myopathy with early-onset Paget disease and frontotemporal dementia inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In some cases, an affected person inherits the mut... |
<s>[INST] Is Wolff-Parkinson-White syndrome inherited ? [/INST] Most cases of Wolff-Parkinson-White syndrome occur in people with no apparent family history of the condition. These cases are described as sporadic and are not inherited. Familial Wolff-Parkinson-White syndrome accounts for only a small percentage of all... |
<s>[INST] Is alpha thalassemia inherited ? [/INST] The inheritance of alpha thalassemia is complex. Each person inherits two alpha-globin alleles from each parent. If both parents are missing at least one alpha-globin allele, their children are at risk of having Hb Bart syndrome, HbH disease, or alpha thalassemia trait... |
<s>[INST] Is KBG syndrome inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In some cases, an affected person inherits the mutation from one affected parent. Other cases result from new mutations ... |
<s>[INST] Is Greenberg dysplasia inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show ... |
<s>[INST] Is familial porencephaly inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. </s> |
<s>[INST] Is psoriatic arthritis inherited ? [/INST] This condition has an unknown inheritance pattern. Approximately 40 percent of affected individuals have at least one close family member with psoriasis or psoriatic arthritis. </s> |
<s>[INST] Is carbamoyl phosphate synthetase I deficiency inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but the... |
<s>[INST] Is rheumatoid arthritis inherited ? [/INST] The inheritance pattern of rheumatoid arthritis is unclear because many genetic and environmental factors appear to be involved. However, having a close relative with rheumatoid arthritis likely increases a person's risk of developing the condition. </s> |
<s>[INST] Is generalized arterial calcification of infancy inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but t... |
<s>[INST] Is PPM-X syndrome inherited ? [/INST] More than 99 percent of PPM-X syndrome cases occur in people with no history of the disorder in their family. Many of these cases result from new mutations in the MECP2 gene. A few families with more than one affected family member have been described. These cases helped... |
<s>[INST] Is spinocerebellar ataxia type 36 inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In most cases, an affected person has one parent with the condition. In conditions that are caused by... |
<s>[INST] Is Niemann-Pick disease inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show... |
<s>[INST] Is RAPADILINO syndrome inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show ... |
<s>[INST] Is steatocystoma multiplex inherited ? [/INST] When steatocystoma multiplex is caused by mutations in the KRT17 gene, it is inherited in an autosomal dominant pattern. Autosomal dominant inheritance means one copy of the altered gene in each cell is sufficient to cause the disorder. In most cases, an affected... |
<s>[INST] Is alpha-mannosidosis inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show s... |
<s>[INST] Is Freeman-Sheldon syndrome inherited ? [/INST] Freeman-Sheldon syndrome can have different inheritance patterns. In some cases, the condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. The condition can also have a... |
<s>[INST] Is severe congenital neutropenia inherited ? [/INST] Most cases of severe congenital neutropenia are classified as sporadic and occur in people with no apparent history of the disorder in their family. Some of these cases are associated with changes in specific genes; however in some cases the cause of the di... |
<s>[INST] Is Vohwinkel syndrome inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In most cases, an affected person inherits the mutation from one affected parent. Other cases result from new muta... |
<s>[INST] Is thanatophoric dysplasia inherited ? [/INST] Thanatophoric dysplasia is considered an autosomal dominant disorder because one mutated copy of the FGFR3 gene in each cell is sufficient to cause the condition. Virtually all cases of thanatophoric dysplasia are caused by new mutations in the FGFR3 gene and occ... |
<s>[INST] Is GRACILE syndrome inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show sig... |
<s>[INST] Is coloboma inherited ? [/INST] Most often, isolated coloboma is not inherited, and there is only one affected individual in a family. However, the affected individual is still at risk of passing the coloboma on to his or her own children. In cases when it is passed down in families, coloboma can have differ... |
<s>[INST] Is Brody myopathy inherited ? [/INST] Brody myopathy is usually inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not sh... |
<s>[INST] Is isolated lissencephaly sequence inherited ? [/INST] The inheritance pattern of ILS depends on the gene involved. When ILS is caused by mutations in the PAFAH1B1 or TUBA1A gene, it is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause th... |
<s>[INST] Is homocystinuria inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. Most often, the parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but do not show signs an... |
<s>[INST] Is X-linked congenital stationary night blindness inherited ? [/INST] This condition is inherited in an X-linked recessive pattern. The NYX and CACNA1F genes are located on the X chromosome, which is one of the two sex chromosomes. In males (who have only one X chromosome), one altered copy of the gene in eac... |
<s>[INST] Is cytogenetically normal acute myeloid leukemia inherited ? [/INST] CN-AML is not usually inherited but arises from genetic changes in the body's cells that occur after conception. Rarely, an inherited mutation in the CEBPA gene causes acute myeloid leukemia. In these cases, the condition follows an autosoma... |
<s>[INST] Is adermatoglyphia inherited ? [/INST] Adermatoglyphia is inherited in an autosomal dominant pattern, which means one copy of the altered SMARCAD1 gene in each cell is sufficient to cause the condition. In many cases, an affected person has one parent with the condition. </s> |
<s>[INST] Is X-linked lissencephaly with abnormal genitalia inherited ? [/INST] This condition is inherited in an X-linked pattern. A condition is considered X-linked if the mutated gene that causes the disorder is located on the X chromosome, one of the two sex chromosomes in each cell. In males (who have only one X c... |
<s>[INST] Is prothrombin thrombophilia inherited ? [/INST] The risk of developing an abnormal clot in a blood vessel depends on whether a person inherits one or two copies of the F2 gene mutation that causes prothrombin thrombophilia. In the general population, the risk of developing an abnormal blood clot is about 1 i... |
<s>[INST] Is catecholaminergic polymorphic ventricular tachycardia inherited ? [/INST] When CPVT results from mutations in the RYR2 gene, it has an autosomal dominant pattern of inheritance. Autosomal dominant inheritance means that one copy of the altered gene in each cell is sufficient to cause the disorder. In about... |
<s>[INST] Is Schinzel-Giedion syndrome inherited ? [/INST] Schinzel-Giedion syndrome results from new mutations in the SETBP1 gene and occurs in people with no history of the disorder in their family. One copy of the altered gene in each cell is sufficient to cause the disorder. </s> |
<s>[INST] Is PRICKLE1-related progressive myoclonus epilepsy with ataxia inherited ? [/INST] Some cases of PRICKLE1-related progressive myoclonus epilepsy with ataxia are inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an au... |
<s>[INST] Is autosomal dominant vitreoretinochoroidopathy inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In most cases, an affected person has one parent with the condition. </s> |
<s>[INST] Is pyruvate carboxylase deficiency inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically ... |
<s>[INST] Is spondyloepiphyseal dysplasia congenita inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. </s> |
<s>[INST] Is palmoplantar keratoderma with deafness inherited ? [/INST] Palmoplantar keratoderma with deafness can have different inheritance patterns. When this disorder is caused by GJB2 gene mutations, it is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficie... |
<s>[INST] Is 47,XYY syndrome inherited ? [/INST] Most cases of 47,XYY syndrome are not inherited. The chromosomal change usually occurs as a random event during the formation of sperm cells. An error in cell division called nondisjunction can result in sperm cells with an extra copy of the Y chromosome. If one of these... |
<s>[INST] Is Leydig cell hypoplasia inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not sh... |
<s>[INST] Is permanent neonatal diabetes mellitus inherited ? [/INST] Permanent neonatal diabetes mellitus can have different inheritance patterns. When this condition is caused by mutations in the KCNJ11 or INS gene it is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cel... |
<s>[INST] Is Camurati-Engelmann disease inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. </s> |
<s>[INST] Is congenital contractural arachnodactyly inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. </s> |
<s>[INST] Is Cole disease inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In most cases of this disorder, an affected person inherits the mutation from one affected parent. Other cases result fr... |
<s>[INST] Is congenital central hypoventilation syndrome inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. More than 90 percent of cases of CCHS result from new mutations in the PHOX2B gene. These... |
<s>[INST] Is Aicardi syndrome inherited ? [/INST] Nearly all known cases of Aicardi syndrome are sporadic, which means that they are not passed down through generations and occur in people with no history of the disorder in their family. The disorder is believed to result from new gene mutations. Aicardi syndrome is c... |
<s>[INST] Is medium-chain acyl-CoA dehydrogenase deficiency inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but ... |
<s>[INST] Is hereditary hemochromatosis inherited ? [/INST] Types 1, 2, and 3 hemochromatosis are inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. Most often, the parents of an individual with an autosomal recessive condition each carry one copy of the mutate... |
<s>[INST] Is incontinentia pigmenti inherited ? [/INST] This condition is inherited in an X-linked dominant pattern. The gene associated with this condition is located on the X chromosome, which is one of the two sex chromosomes. In females (who have two X chromosomes), a mutation in one of the two copies of the gene i... |
<s>[INST] Is Stve-Wiedemann syndrome inherited ? [/INST] This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not s... |
<s>[INST] Is autoimmune lymphoproliferative syndrome inherited ? [/INST] In most people with ALPS, including the majority of those with FAS gene mutations, this condition is inherited in an autosomal dominant pattern, which means one copy of an altered gene in each cell is sufficient to cause the disorder. In these cas... |
<s>[INST] Is SOX2 anophthalmia syndrome inherited ? [/INST] SOX2 anophthalmia syndrome is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. Most cases result from new mutations in the SOX2 gene and occur in people with no history of th... |
<s>[INST] Is spastic paraplegia type 31 inherited ? [/INST] This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. </s> |
<s>[INST] Is microphthalmia with linear skin defects syndrome inherited ? [/INST] This condition is inherited in an X-linked dominant pattern. The gene associated with this condition is located on the X chromosome, which is one of the two sex chromosomes. In females (who have two X chromosomes), a mutation in one of th... |
<s>[INST] Is dystrophic epidermolysis bullosa inherited ? [/INST] The most severe types of dystrophic epidermolysis bullosa are inherited in an autosomal recessive pattern. Autosomal recessive inheritance means that both copies of the COL7A1 gene in each cell have mutations. Most often, the parents of an individual wit... |
<s>[INST] Is Leber congenital amaurosis inherited ? [/INST] Leber congenital amaurosis usually has an autosomal recessive pattern of inheritance. Autosomal recessive inheritance means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one c... |
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