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Summary Literature (0)
MIM:614582 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9; COXPD9

Xenbase Genes: mrpl3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013811 - combined oxidative phosphorylation defect type 9

Disease Ontology (DO):
DOID:0060286 - combined oxidative phosphorylation deficiency
DOID:0111472 - combined oxidative phosphorylation deficiency 9