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Summary Literature (0)
MIM:618839 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 42; COXPD42

Xenbase Genes:

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0030008 - combined oxidative phosphorylation deficiency 42

Disease Ontology (DO):
DOID:0112118 - combined oxidative phosphorylation deficiency 42