Mitochondrial complex III deficiency nuclear type 6

Definition

Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the CYC1 gene.

Also known as CYC1 mitochondrial complex III deficiency, mitochondrial complex III deficiency caused by mutation in CYC1 — per MONDO

Also identified as

• DOID 0080115 per MONDO
• OMIM 615453 per MONDO
• UMLS C3809553 per MONDO