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Summary Literature (0)
MIM:616811 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29; COXPD29

Xenbase Genes: txn2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014781 - combined oxidative phosphorylation deficiency 29

Disease Ontology (DO):
DOID:0111501 - combined oxidative phosphorylation deficiency 29