Term Name:	familial apolipoprotein C-II deficiency
Synonyms:	C-II anapolipoproteinemia, familial apoC-II deficiency, familial APOC2 deficiency, hyperlipoproteinemia, type 1b, hyperlipoproteinemia, type Ib
Definition:	A familial chylomicronemia syndrome characterized by onset in adolescence or adulthood of hypertriglyceridemia and fasting chylomicronemia that has_material_basis_in homozygous or compound heterozygous mutation in the APOC2 gene on chromosome 19q13.32.
Ontology:	Human Disease [DOID:0111418]   ( DOID:0111418 )