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Summary Literature (0)
MIM:612016 - COENZYME Q10 DEFICIENCY, PRIMARY, 4; COQ10D4

Xenbase Genes: coq8a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012784 - autosomal recessive ataxia due to ubiquinone deficiency

Disease Ontology (DO):
DOID:0050730 - coenzyme Q10 deficiency disease
DOID:0070241 - primary coenzyme Q10 deficiency 4