Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:613559 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7

Xenbase Genes: mtrfr

Human Disease Resource: MIM

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