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Summary Literature (0)
MIM:614922 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11

Xenbase Genes: rmnd1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013969 - combined oxidative phosphorylation defect type 11

Disease Ontology (DO):
DOID:0060286 - combined oxidative phosphorylation deficiency
DOID:0111481 - combined oxidative phosphorylation deficiency 11