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Summary Literature (0)
MIM:616974 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30; COXPD30

Xenbase Genes: trmt10c

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014856 - combined oxidative phosphorylation defect type 30

Disease Ontology (DO):
DOID:0111471 - combined oxidative phosphorylation deficiency 30