" /> Hyperlipidemia, familial combined, 2 - CISMeF





Preferred Label : Hyperlipidemia, familial combined, 2;

Symbol : FCHL2;

CISMeF acronym : FCHL2; HYPLIP2;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Hyperlipidemia, combined, 2; HYPLIP2;

Description : For a phenotypic description and a discussion of genetic heterogeneity of familial combined hyperlipidemia (FCHL), see 144250. Familial combined hyperlipidemia is a common familial lipid disorder characterized by a variable pattern of elevated levels of plasma cholesterol and/or triglycerides. It is present in 10 to 20% of patients with premature coronary artery disease.;

Prefixed ID : %604499;

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27/07/2025


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