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Summary Literature (0)
MIM:614654 - COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5

Xenbase Genes: coq9

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013840 - encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome

Disease Ontology (DO):
DOID:0050730 - coenzyme Q10 deficiency disease
DOID:0070242 - primary coenzyme Q10 deficiency 5