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Summary Literature (0)
MIM:616276 - COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7

Xenbase Genes: coq4

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014562 - neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome

Disease Ontology (DO):
DOID:0070244 - primary coenzyme Q10 deficiency 7