Mitochondrial complex III deficiency nuclear type 8

Definition

Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the LYRM7 gene.

Also known as LYRM7 mitochondrial complex III deficiency, mitochondrial complex III deficiency caused by mutation in LYRM7, mitochondrial complex III deficiency nuclear type 8 — per MONDO

Also identified as

• DOID 0080117 per MONDO
• OMIM 615838 per MONDO
• UMLS C4014440 per MONDO