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Summary Literature (0)
DOID:13809 - familial combined hyperlipidemia


Disease Ontology Definition:n_a

Synonyms: familial combined hyperlipidemia (disorder), familial combined hyperlipidemia (disorder) [Ambiguous], familial multiple lipoprotein-type hyperlipidemia, familial multiple lipoprotein-type hyperlipidemia (disorder), hyperbetalipoproteinemia with prebetalipoproteinemia, mixed hyperlipidaemia, mixed hyperlipidemia, mixed hyperlipidemia (disorder), type IIb hyperlipoproteinemia

Xenbase Genes : lpl, usf1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0001807 - familial combined hyperlipidemia

OMIM:
OMIM:144250 - HYPERLIPIDEMIA, FAMILIAL COMBINED, 3; FCHL3

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

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