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Summary Literature (0)
MIM:617664 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32

Xenbase Genes: mrps34

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054654 - combined oxidative phosphorylation deficiency 32

Disease Ontology (DO):
DOID:0111492 - combined oxidative phosphorylation deficiency 32