Home Page
Orphanet References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 23/12/2008
Symbol APOC3
Location 11q23.3
Name hyperalphalipoproteinemia with APOC3 deficiency
Corresponding gene APOC3
Main clinical features
  • plasma concentrations of HDL cholesterol and APOA1 above the 95th percentile for sex-matched controls
  • Genetic determination not applicable
    Function/system disorder metabolism/lipoprotein-lipid
    Type disease
    Gene product
    Name apolipoprotein C-III (APOC3)
    Remark(s)