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Summary Literature (0)
MIM:615918 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21; COXPD21

Xenbase Genes: tars2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014398 - combined oxidative phosphorylation defect type 21

Disease Ontology (DO):
DOID:0060286 - combined oxidative phosphorylation deficiency
DOID:0111465 - combined oxidative phosphorylation deficiency 21