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DOID:0111421 - familial apolipoprotein A5 deficiency
Disease Ontology 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.
Synonyms: familial APOA5 deficiency, familial apolipoprotein A-V deficiency,
Xenbase Genes : apoa5
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee