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Summary Literature (0)
MIM:616045 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22; COXPD22

Xenbase Genes: atp5f1a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0020727 - combined oxidative phosphorylation deficiency 22

Disease Ontology (DO):
DOID:0111498 - combined oxidative phosphorylation deficiency 22