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Summary Literature (0)
MIM:300816 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6

Xenbase Genes: aifm1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010437 - severe X-linked mitochondrial encephalomyopathy

Disease Ontology (DO):
DOID:0111502 - combined oxidative phosphorylation deficiency 6