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;
Origin ID : 604499;
UMLS CUI : C1858308;
Currated CISMeF NLP mapping
- Semantic type(s)
- UMLS correspondences (same concept)
