Term Name: apolipoprotein C-III deficiency
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.
Ontology: Human Disease [DOID:0111370]   ( DOID:0111370 )

Relationships
is a type of: autosomal dominant disease cholesterol-ester transfer protein deficiency