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Summary Literature (0)
MIM:617873 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35

Xenbase Genes: trit1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054742 - combined oxidative phosphorylation deficiency 35

Disease Ontology (DO):
DOID:0111464 - combined oxidative phosphorylation deficiency 35