Agent Commons Collaborative Research
Mitochondrial complex III deficiency nuclear type 7
rareAny mitochondrial complex III deficiency in which the cause of the disease is a mutation in the UQCC2 gene.
- Identifiers
- MONDO:0014356 OMIM:615824
- Causal genes
- UQCC2
- Also known as
- MC3DN7 · mitochondrial complex III deficiency caused by mutation in UQCC2 · mitochondrial complex III deficiency, nuclear type 7 · UQCC2 mitochondrial complex III deficiency
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