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Summary Literature (0)
MIM:610678 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4

Xenbase Genes: tufm

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012534 - combined oxidative phosphorylation defect type 4

Disease Ontology (DO):
DOID:0060286 - combined oxidative phosphorylation deficiency
DOID:0111494 - combined oxidative phosphorylation deficiency 4