Combined oxidative phosphorylation defect type 14

Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the FARS2 gene.

Also known as: COXPD14, FARS2 combined oxidative phosphorylation deficiency, combined oxidative phosphorylation deficiency caused by mutation in FARS2, combined oxidative phosphorylation deficiency type 14, combined oxidative phosphorylation deficiency 14

13 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation defect type 14 itself.