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The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child. There are over 6,000 known genetic disorders in humans.
Indian Genetic Disease Database; Infantile cerebellar retinal degeneration; Infantile cortical hyperostosis; Inherited thrombotic thrombocytopenic purpura; Intellectual disability-spasticity-ectrodactyly syndrome; Iris hypoplasia with glaucoma; Isolated hyperCKemia
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Online Mendelian Inheritance in Man (OMIM) is a continuously updated catalog of human genes and genetic disorders and traits, with a particular focus on the gene-phenotype relationship. As of 28 June 2019 [update] , approximately 9,000 of the over 25,000 entries in OMIM represented phenotypes ; the rest represented genes , many of which were ...
There are well over 6,000 known genetic disorders, [4] and new genetic disorders are constantly being described in medical literature. [5] More than 600 genetic disorders are treatable. [ 6 ] Around 1 in 50 people are affected by a known single-gene disorder, while around 1 in 263 are affected by a chromosomal disorder . [ 7 ]
List of human disease case fatality rates; List of notifiable diseases - diseases that should be reported to public health services, e.g., hospitals. Lists of plant diseases; List of pollution-related diseases; List of skin conditions; List of diseases by year of discovery; Disorders. List of communication disorders; List of genetic disorders ...
Autosomal dominant Charcot–Marie–Tooth disease type 2 with giant axons Autosomal dominant GTP cyclohydrolase I deficiency Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
C. Camera–Marugo–Cohen syndrome; Camptodactyly-arthropathy-coxa vara-pericarditis syndrome; Camptodactyly-taurinuria syndrome; Camptodactyly, tall stature, and hearing loss syndrome