Combined oxidative phosphorylation defect type 26

Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the TRMT5 gene.

Also known as: COXPD26, TRMT5 combined oxidative phosphorylation deficiency, combined oxidative phosphorylation deficiency caused by mutation in TRMT5, combined oxidative phosphorylation deficiency type 26, combined oxidative phosphorylation deficiency 26

13 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation defect type 26 itself.