Combined oxidative phosphorylation defect type 20

Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the VARS2 gene.

Also known as: COXPD20, VARS2 combined oxidative phosphorylation deficiency, combined oxidative phosphorylation deficiency caused by mutation in VARS2, combined oxidative phosphorylation deficiency type 20, combined oxidative phosphorylation deficiency 20

13 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation defect type 20 itself.