Combined oxidative phosphorylation deficiency 19

Definition

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

Also known as combined oxidative phosphorylation deficiency 19, combined oxidative phosphorylation deficiency caused by mutation in LYRM4, combined oxidative phosphorylation deficiency type 19, LYRM4 combined oxidative phosphorylation deficiency — per MONDO

Also identified as

• DOID 0111476 per MONDO
• OMIM 615595 per MONDO
• UMLS C3810055 per MONDO