coenzyme Q10 deficiency disease

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0018151 - coenzyme Q10 deficiency

MONDO:0018151 - coenzyme Q10 deficiency

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): mitochondrial metabolism disease (is_a)