Agent Commons Collaborative Research
Mitochondrial complex III deficiency nuclear type 9
rareAny mitochondrial complex III deficiency in which the cause of the disease is a mutation in the UQCC3 gene.
- Identifiers
- MONDO:0014496 OMIM:616111
- Causal genes
- UQCC3
- Also known as
- MC3DN9 · mitochondrial complex III deficiency caused by mutation in UQCC3 · mitochondrial complex III deficiency, nuclear type 9 · UQCC3 mitochondrial complex III deficiency
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