Summary Literature (0)

DOID:0070245 - primary coenzyme Q10 deficiency 8

Disease Ontology Definition:A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the COQ7 gene on chromosome 16p12.3.

Synonyms: coenzyme Q10 deficiency, primary, 8, COQ10D8

Xenbase Genes : coq7

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014754 - primary coenzyme Q10 deficiency 8

MIM:

MIM:616733 - COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8

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

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