OBO ID: DOID:0111370
Term Name: apolipoprotein C-III deficiency Search Ontology:
Synonyms:
  • HALP2
  • hyperalphalipoproteinemia 2
Definition: A cholesterol-ester transfer protein deficiency characterized by elevated levels of alpha-lipoprotein in the blood that has_material_basis_in heterozygous mutation in the APOC3 gene on chromosome 11q23.3. https://www.ncbi.nlm.nih.gov/pubmed/2022742
References:
Ontology: Human Disease   ( DOID:0111370 )
OTHER apolipoprotein C-III deficiency PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
APOC3 Apolipoprotein C-III deficiency
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None