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Summary Literature (0)
MIM:614650 - COENZYME Q10 DEFICIENCY, PRIMARY, 6; COQ10D6

Xenbase Genes: coq6

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013836 - familial steroid-resistant nephrotic syndrome with sensorineural deafness

Disease Ontology (DO):
DOID:0050730 - coenzyme Q10 deficiency disease
DOID:0070243 - primary coenzyme Q10 deficiency 6