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Summary Literature (0)
MIM:616239 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24

Xenbase Genes: nars2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014547 - combined oxidative phosphorylation defect type 24

Disease Ontology (DO):
DOID:0111485 - combined oxidative phosphorylation deficiency 24