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Mitochondrial complex III deficiency nuclear type 6
rareAny mitochondrial complex III deficiency in which the cause of the disease is a mutation in the CYC1 gene.
- Identifiers
- MONDO:0014194 OMIM:615453
- Causal genes
- CYC1
- Also known as
- CYC1 mitochondrial complex III deficiency · MC3DN6 · mitochondrial complex III deficiency caused by mutation in CYC1 · mitochondrial complex III deficiency, nuclear type 6
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