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Summary Literature (0)
MIM:616430 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25

Xenbase Genes: mars2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014636 - combined oxidative phosphorylation defect type 25

Disease Ontology (DO):
DOID:0111468 - combined oxidative phosphorylation deficiency 25