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Summary Literature (0)
MIM:610498 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2

Xenbase Genes: mrps16

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012510 - combined oxidative phosphorylation defect type 2

Disease Ontology (DO):
DOID:0060286 - combined oxidative phosphorylation deficiency
DOID:0111483 - combined oxidative phosphorylation deficiency 2