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Summary Literature (0)
MIM:613559 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7

Xenbase Genes: mtrfr

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013306 - combined oxidative phosphorylation defect type 7

Disease Ontology (DO):
DOID:0060286 - combined oxidative phosphorylation deficiency
DOID:0111487 - combined oxidative phosphorylation deficiency 7