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Summary Literature (0)
MIM:615917 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20; COXPD20

Xenbase Genes: vars2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014397 - combined oxidative phosphorylation defect type 20

Disease Ontology (DO):
DOID:0111478 - combined oxidative phosphorylation deficiency 20