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Summary Literature (0)
DOID:0050730 - coenzyme Q10 deficiency disease


Disease Ontology Definition:A mitochondrial metabolism disease that is characterized by a deficiency of CoQ10 resulting from reduced biosynthesis.

Synonyms: COENZYME Q10 DEFICIENCY, PRIMARY

Xenbase Genes : coq7, pdss2, coq6, coq8a, coq9, coq2, pdss1, aptx, coq4

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018151 - coenzyme Q10 deficiency

OMIM:
OMIM:607426 - COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1
OMIM:612016 - COENZYME Q10 DEFICIENCY, PRIMARY, 4; COQ10D4
OMIM:614650 - COENZYME Q10 DEFICIENCY, PRIMARY, 6; COQ10D6
OMIM:614654 - COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): mitochondrial metabolism disease (is_a)