{"id":115036,"date":"2021-06-27T07:41:25","date_gmt":"2021-06-27T07:41:25","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=115036"},"modified":"2021-06-27T07:41:25","modified_gmt":"2021-06-27T07:41:25","slug":"autosomal-dominant-disease","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-dominant-disease\/","title":{"rendered":"Autosomal dominant disease"},"content":{"rendered":"<p>Disorder caused by a dominant mutant (abnormal) gene on an autosome (nonsex chromosome). Evidence of the disorder may not occur for several decades. The mutant gene is inherited from one or both parents or is the result of a fresh mutation. If both parents have the mutant dominant gene, all offspring will be affected; if one parent is affected, 50% of the offspring will be affected; the normal children of an affected parent do not carry the trait.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Disorder caused by a dominant mutant (abnormal) gene on an autosome (nonsex chromosome). Evidence of the disorder may not occur for several decades. The mutant gene is inherited from one or both parents or is the result of a fresh mutation. If both parents have the mutant dominant gene, all offspring will be affected; if [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-115036","post","type-post","status-publish","format-standard","hentry","category-a"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Autosomal dominant disease - Definition of Autosomal dominant disease<\/title>\n<meta name=\"description\" content=\"Disorder caused by a dominant mutant (abnormal) gene on an autosome (nonsex chromosome). Evidence of the disorder may not occur for several decades. The mutant gene is inherited from one or both parents or is the result of a fresh mutation. 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