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Summary Literature (0)
MIM:607426 - COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1

Xenbase Genes: pdss2, coq8a, pdss1, aptx, coq2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011829 - coenzyme Q10 deficiency, primary, 1
MONDO:0016816 - obsolete Leigh syndrome with nephrotic syndrome

Disease Ontology (DO):
DOID:0050730 - coenzyme Q10 deficiency disease
DOID:0070238 - primary coenzyme Q10 deficiency 1