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"Cirrhosis," familial
- ... not seen in every generation of an affected family. cystic fibrosis , sickle cell disease X-linked dominant X-linked ...
- ... mutations) in a single gene, such as cystic fibrosis and sickle cell disease . While a family health history provides information about the risk of ...
- ... disorder of glycosylation , also called PMM2 -CDG Cystic fibrosis D-bifunctional protein deficiency Dihydrolipoamide dehydrogenase deficiency Familial dysautonomia Congenital hyperinsulinism , also called familial hyperinsulinism Familial ...
- ... example, hypermanganesemia with dystonia , polycythemia vera , and ... example, familial Mediterranean fever , which occurs mainly in populations bordering ...
- ... disorders, such as sickle cell disease and cystic fibrosis , are caused by variants (also known as mutations) ... multifactorial disorders. Although complex disorders often cluster in families, they do not have a clear-cut pattern ...
- ... carrier status for less common conditions, including cystic fibrosis and sickle cell disease . A carrier is someone ... come from, their ethnicity, and genetic connections between families. For more information, see What is genetic ancestry ...
