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DOID:3145 - hyperlipoproteinemia type III
Disease Ontology Definition:A familial hyperlipidemia that has_material_basis_in by homozygous, compound heterozygous, or heterozygous mutation in the APOE gene on chromosome 19q13.
Synonyms: Remnant hyperlipidemia, carbohydrate induced hyperlipemia, familial hypercholesterolaemia with hyperlipaemia, familial type 3 hyperlipoproteinemia, familial type 3 hyperlipoproteinemia (disorder),
Xenbase Genes : apoe
MONDO:0018473 - hyperlipoproteinemia type 3 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
familial hyperlipidemia (is_a)