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Disease Ontology Browser
familial apolipoprotein A5 deficiency (DOID:0111421)
Alliance: disease page
Synonyms: familial APOA5 deficiency; familial apolipoprotein A-V deficiency
Alt IDs: OMIM:144650, ORDO:530849
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/10/2024
MGI 6.24 		The Jackson Laboratory