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Summary Literature (0)
MIM:609060 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1

Xenbase Genes: gfm1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012191 - hepatoencephalopathy due to combined oxidative phosphorylation defect type 1

Disease Ontology (DO):
DOID:0060286 - combined oxidative phosphorylation deficiency
DOID:0111474 - combined oxidative phosphorylation deficiency 1