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Echinobase
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,

Echinobase Genes : coq2, coq6


OMIM:
MIM:607426 - coenzyme q10 deficiency, primary, 1; coq10d1
MIM:612016 - coenzyme q10 deficiency, primary, 4; coq10d4
MIM:614650 - coenzyme q10 deficiency, primary, 6; coq10d6
MIM: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)