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Summary Literature (0)
MIM:615440 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17; COXPD17

Xenbase Genes: elac2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014190 - combined oxidative phosphorylation defect type 17

Disease Ontology (DO):
DOID:0111496 - combined oxidative phosphorylation deficiency 17