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