{"id":115038,"date":"2021-06-27T07:44:47","date_gmt":"2021-06-27T07:44:47","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=115038"},"modified":"2021-06-27T07:44:47","modified_gmt":"2021-06-27T07:44:47","slug":"autosomal-recessive-disease","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/","title":{"rendered":"Autosomal recessive disease"},"content":{"rendered":"<p>Disorder caused by the presence of two recessive (homozygous) mutant (abnormal) genes on an autosome. If only one mutant recessive (heterozygous) gene is present the person is not affected with the disease but is a carrier of it. One fourth of the children of two heterozygous (carrier) parents will be affected and another one half will be carriers. All of the children of two homozygous affected persons will be affected. The children of one normal and one affected with the disease will all be carriers. When close relatives (e.g., first cousins) marry, the chance that an offspring will inherit an abnormal recessive gene from both parents is increased, as it is among persons marrying within certain ethnic groups (e.g.,Tay- Sachs disease among Ashkenazic Jews).<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Disorder caused by the presence of two recessive (homozygous) mutant (abnormal) genes on an autosome. If only one mutant recessive (heterozygous) gene is present the person is not affected with the disease but is a carrier of it. One fourth of the children of two heterozygous (carrier) parents will be affected and another one half [&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-115038","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 recessive disease - Definition of Autosomal recessive disease<\/title>\n<meta name=\"description\" content=\"Disorder caused by the presence of two recessive (homozygous) mutant (abnormal) genes on an autosome. If only one mutant recessive (heterozygous) gene is present the person is not affected with the disease but is a carrier of it. One fourth of the children of two heterozygous (carrier) parents will be affected and another one half will be carriers. All of the children of two homozygous affected persons will be affected. The children of one normal and one affected with the disease will all be carriers. When close relatives (e.g., first cousins) marry, the chance that an offspring will inherit an abnormal recessive gene from both parents is increased, as it is among persons marrying within certain ethnic groups (e.g.,Tay- Sachs disease among Ashkenazic Jews).\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Autosomal recessive disease - Definition of Autosomal recessive disease\" \/>\n<meta property=\"og:description\" content=\"Disorder caused by the presence of two recessive (homozygous) mutant (abnormal) genes on an autosome. If only one mutant recessive (heterozygous) gene is present the person is not affected with the disease but is a carrier of it. One fourth of the children of two heterozygous (carrier) parents will be affected and another one half will be carriers. All of the children of two homozygous affected persons will be affected. The children of one normal and one affected with the disease will all be carriers. When close relatives (e.g., first cousins) marry, the chance that an offspring will inherit an abnormal recessive gene from both parents is increased, as it is among persons marrying within certain ethnic groups (e.g.,Tay- Sachs disease among Ashkenazic Jews).\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/\" \/>\n<meta property=\"og:site_name\" content=\"Glossary\" \/>\n<meta property=\"article:published_time\" content=\"2021-06-27T07:44:47+00:00\" \/>\n<meta name=\"author\" content=\"Glossary\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Glossary\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/\",\"url\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/\",\"name\":\"Autosomal recessive disease - Definition of Autosomal recessive disease\",\"isPartOf\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#website\"},\"datePublished\":\"2021-06-27T07:44:47+00:00\",\"dateModified\":\"2021-06-27T07:44:47+00:00\",\"author\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5\"},\"description\":\"Disorder caused by the presence of two recessive (homozygous) mutant (abnormal) genes on an autosome. If only one mutant recessive (heterozygous) gene is present the person is not affected with the disease but is a carrier of it. One fourth of the children of two heterozygous (carrier) parents will be affected and another one half will be carriers. All of the children of two homozygous affected persons will be affected. The children of one normal and one affected with the disease will all be carriers. When close relatives (e.g., first cousins) marry, the chance that an offspring will inherit an abnormal recessive gene from both parents is increased, as it is among persons marrying within certain ethnic groups (e.g.,Tay- Sachs disease among Ashkenazic Jews).\",\"breadcrumb\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Autosomal recessive disease\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#website\",\"url\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/\",\"name\":\"Glossary\",\"description\":\"Difinitions\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/?s={search_term_string}\"},\"query-input\":\"required name=search_term_string\"}],\"inLanguage\":\"en-US\"},{\"@type\":\"Person\",\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5\",\"name\":\"Glossary\",\"url\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/author\/adminglossary\/\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Autosomal recessive disease - Definition of Autosomal recessive disease","description":"Disorder caused by the presence of two recessive (homozygous) mutant (abnormal) genes on an autosome. If only one mutant recessive (heterozygous) gene is present the person is not affected with the disease but is a carrier of it. One fourth of the children of two heterozygous (carrier) parents will be affected and another one half will be carriers. All of the children of two homozygous affected persons will be affected. The children of one normal and one affected with the disease will all be carriers. When close relatives (e.g., first cousins) marry, the chance that an offspring will inherit an abnormal recessive gene from both parents is increased, as it is among persons marrying within certain ethnic groups (e.g.,Tay- Sachs disease among Ashkenazic Jews).","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/","og_locale":"en_US","og_type":"article","og_title":"Autosomal recessive disease - Definition of Autosomal recessive disease","og_description":"Disorder caused by the presence of two recessive (homozygous) mutant (abnormal) genes on an autosome. If only one mutant recessive (heterozygous) gene is present the person is not affected with the disease but is a carrier of it. One fourth of the children of two heterozygous (carrier) parents will be affected and another one half will be carriers. All of the children of two homozygous affected persons will be affected. The children of one normal and one affected with the disease will all be carriers. When close relatives (e.g., first cousins) marry, the chance that an offspring will inherit an abnormal recessive gene from both parents is increased, as it is among persons marrying within certain ethnic groups (e.g.,Tay- Sachs disease among Ashkenazic Jews).","og_url":"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/","og_site_name":"Glossary","article_published_time":"2021-06-27T07:44:47+00:00","author":"Glossary","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Glossary","Est. reading time":"1 minute"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/","url":"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/","name":"Autosomal recessive disease - Definition of Autosomal recessive disease","isPartOf":{"@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/#website"},"datePublished":"2021-06-27T07:44:47+00:00","dateModified":"2021-06-27T07:44:47+00:00","author":{"@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5"},"description":"Disorder caused by the presence of two recessive (homozygous) mutant (abnormal) genes on an autosome. If only one mutant recessive (heterozygous) gene is present the person is not affected with the disease but is a carrier of it. One fourth of the children of two heterozygous (carrier) parents will be affected and another one half will be carriers. All of the children of two homozygous affected persons will be affected. The children of one normal and one affected with the disease will all be carriers. When close relatives (e.g., first cousins) marry, the chance that an offspring will inherit an abnormal recessive gene from both parents is increased, as it is among persons marrying within certain ethnic groups (e.g.,Tay- Sachs disease among Ashkenazic Jews).","breadcrumb":{"@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/autosomal-recessive-disease\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.healthbenefitstimes.com\/glossary\/"},{"@type":"ListItem","position":2,"name":"Autosomal recessive disease"}]},{"@type":"WebSite","@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/#website","url":"https:\/\/www.healthbenefitstimes.com\/glossary\/","name":"Glossary","description":"Difinitions","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.healthbenefitstimes.com\/glossary\/?s={search_term_string}"},"query-input":"required name=search_term_string"}],"inLanguage":"en-US"},{"@type":"Person","@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5","name":"Glossary","url":"https:\/\/www.healthbenefitstimes.com\/glossary\/author\/adminglossary\/"}]}},"_links":{"self":[{"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/posts\/115038","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/comments?post=115038"}],"version-history":[{"count":1,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/posts\/115038\/revisions"}],"predecessor-version":[{"id":115039,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/posts\/115038\/revisions\/115039"}],"wp:attachment":[{"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/media?parent=115038"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/categories?post=115038"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/tags?post=115038"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}