Mitochondrial complex III deficiency nuclear type 9

Definition

Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the UQCC3 gene.

Also known as mitochondrial complex III deficiency caused by mutation in UQCC3, UQCC3 mitochondrial complex III deficiency — per MONDO

Also identified as

• DOID 0080118 per MONDO
• OMIM 616111 per MONDO
• UMLS C4015253 per MONDO