{"id":108267,"date":"2021-05-25T06:14:13","date_gmt":"2021-05-25T06:14:13","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=108267"},"modified":"2021-05-25T06:14:13","modified_gmt":"2021-05-25T06:14:13","slug":"congenital-afibrinogenemia","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/congenital-afibrinogenemia\/","title":{"rendered":"Congenital afibrinogenemia"},"content":{"rendered":"<p>Congenital afibrinogenemia is a rare blood disorder that causes improper clotting of the blood. It is also referred to as hypofibrinogenemia. Afibrinogenemia is an inherited condition that is caused by an autosomal recessive gene. It is found in both males and females.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Congenital afibrinogenemia is a rare blood disorder that causes improper clotting of the blood. It is also referred to as hypofibrinogenemia. Afibrinogenemia is an inherited condition that is caused by an autosomal recessive gene. It is found in both males and females. &nbsp;<\/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-108267","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>Congenital afibrinogenemia - Definition of Congenital afibrinogenemia<\/title>\n<meta name=\"description\" content=\"Congenital afibrinogenemia is a rare blood disorder that causes improper clotting of the blood. It is also referred to as hypofibrinogenemia. Afibrinogenemia is an inherited condition that is caused by an autosomal recessive gene. 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