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Summary Literature (0)
MIM:614702 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10; COXPD10

Xenbase Genes: mto1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013865 - mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency

Disease Ontology (DO):
DOID:0111480 - combined oxidative phosphorylation deficiency 10