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autosomal dominant |
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Autosomal dominant or autosomal recessive
Refers to the inheritance pattern of a gene on a chromosome other than X or Y. Genes are inherited in pairs—one gene from each parent. However, the inheritance may not be equal, and one gene may overshadow the other in determining the final form of the encoded characteristic. The gene that overshadows the other is called the dominant gene; the overshadowed gene is the recessive one. Mentioned in: Cerebral Amyloid Angiopathy, Hereditary Hemorrhagic Telangiectasia, Ichthyosis, Muscular Dystrophy, Peripheral Neuropathy, Porphyrias, Prolonged QT Syndrome, Tourette Syndrome, Von Willebrand Disease, Waldenström's Macroglobulinemia
autosomal dominant Genetics Referring to a mode of inheritance, in which the presence of only one copy of a gene of interest on one of the 22 autosomal–non-sex chromosomes, will result in the phenotypic expression of that gene; the
likelihood of expressing an autosomal gene in progeny is 1:2; ♂ and ♀ are affected equally. Cf Autosomal recessive, X-linked recessive. Want to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit the webmaster's page for free fun content. |
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