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Summary Literature (0)
MIM:616794 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28; COXPD28

Xenbase Genes: slc25a26

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014775 - prosomere

Disease Ontology (DO):
DOID:0111470 - combined oxidative phosphorylation deficiency 28