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Summary Literature (0)
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: carbohydrate induced hyperlipemia, Remnant hyperlipidemia, familial type 3 hyperlipoproteinemia (disorder), familial hypercholesterolaemia with hyperlipaemia, familial type 3 hyperlipoproteinemia

Xenbase Genes : apoe

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018473 - hyperlipoproteinemia type 3

MIM:
MIM:617347 - HYPERLIPOPROTEINEMIA, TYPE III

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): familial hyperlipidemia (is_a)