ZFIN Human Disease: familial apolipoprotein A5 deficiency

OBO ID: DOID:0111421

Term Name:	familial apolipoprotein A5 deficiency		Search Ontology:
Synonyms:	familial APOA5 deficiency familial apolipoprotein A-V deficiency
Definition:	A familial chylomicronemia syndrome characterized by hyperchylomicronemia, elevated levels of very low density lipoprotein, and decreased LDL and HDL levels after fasting that has_material_basis_in heterozygous mutation in the APOA5 gene on chromosome 11q23.3. (2)
References:	OMIM:144650 ORDO:530849
Ontology:	Human Disease ( DOID:0111421 )

Relationships

is a type of:	autosomal dominant disease familial chylomicronemia syndrome autosomal dominant disease familial chylomicronemia syndrome Show first 5 Terms

OTHER familial apolipoprotein A5 deficiency PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
APOA5		Hyperchylomicronemia, late-onset

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None