Search Ontology:
Human Disease

apolipoprotein C-III deficiency

Term ID
DOID:0111370
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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