MONDO_0014190 (combined oxidative phosphorylation defect type 17) is any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the ELAC2 gene. Also known as: COXPD17, ELAC2 combined oxidative phosphorylation deficiency, combined oxidative phosphorylation deficiency caused by mutation in ELAC2, combined oxidative phosphorylation deficiency type 17.