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Summary Literature (0)
MIM:614946 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14

Xenbase Genes: fars2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013986 - combined oxidative phosphorylation defect type 14

Disease Ontology (DO):
DOID:0060286 - combined oxidative phosphorylation deficiency
DOID:0111477 - combined oxidative phosphorylation deficiency 14