Combined oxidative phosphorylation defect type 30

Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the TRMT10C gene.

Also known as: COXPD30, TRMT10C combined oxidative phosphorylation deficiency, combined oxidative phosphorylation deficiency 30, combined oxidative phosphorylation deficiency caused by mutation in TRMT10C, combined oxidative phosphorylation deficiency type 30

13 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation defect type 30 itself.