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Summary Literature (0)
MIM:617950 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36; COXPD36

Xenbase Genes: mrps2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054781 - combined oxidative phosphorylation deficiency 36

Disease Ontology (DO):
DOID:0111482 - combined oxidative phosphorylation deficiency 36