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Summary Literature (0)
MIM:614652 - COENZYME Q10 DEFICIENCY, PRIMARY, 3; COQ10D3

Xenbase Genes: pdss2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013838 - coenzyme Q10 deficiency, primary, 3
MONDO:0016816 - obsolete Leigh syndrome with nephrotic syndrome

Disease Ontology (DO):
DOID:0070240 - primary coenzyme Q10 deficiency 3