|
DOID:0111368 - cholesterol-ester transfer protein deficiency
Disease Ontology Definition:A lipid metabolism disorder characterized by elevated levels of alpha-lipoprotein in the blood.
Synonyms: CEPT deficiency, familial hyperalphalipoproteinemia
Xenbase Genes

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
lipid metabolism disorder (is_a)