Combined oxidative phosphorylation deficiency 19

Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the LYRM4 gene.

Also known as: LYRM4 combined oxidative phosphorylation deficiency, combined oxidative phosphorylation deficiency 19, combined oxidative phosphorylation deficiency caused by mutation in LYRM4, combined oxidative phosphorylation deficiency type 19, COXPD19

13 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation deficiency 19 itself.