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Summary Literature (0)
MIM:616198 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23; COXPD23

Xenbase Genes: gtpbp3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014525 - combined oxidative phosphorylation defect type 23

Disease Ontology (DO):
DOID:0111500 - combined oxidative phosphorylation deficiency 23