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Summary Literature (0)
MIM:618835 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 40; COXPD40

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0030006 - combined oxidative phosphorylation deficiency 40

Disease Ontology (DO):
DOID:0112117 - combined oxidative phosphorylation deficiency 40