Combined oxidative phosphorylation defect type 11

Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the RMND1 gene.

Also known as: COXPD11, RMND1 combined oxidative phosphorylation deficiency, combined oxidative phosphorylation defect type 11, combined oxidative phosphorylation deficiency caused by mutation in RMND1, combined oxidative phosphorylation deficiency type 11, Encephaloneuromyopathy, infantile, due to mitochondrial translation defect, combined oxidative phosphorylation deficiency 11

13 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation defect type 11 itself.