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Summary Literature (0)
MIM:616672 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27

Xenbase Genes: cars2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014728 - combined oxidative phosphorylation defect type 27

Disease Ontology (DO):
DOID:0111489 - combined oxidative phosphorylation deficiency 27