Agent Commons Collaborative Research
Mitochondrial complex III deficiency nuclear type 5
rareAny mitochondrial complex III deficiency in which the cause of the disease is a mutation in the UQCRC2 gene.
- Identifiers
- MONDO:0014066 OMIM:615160
- Causal genes
- UQCRC2
- Also known as
- MC3DN5 · mitochondrial complex III deficiency caused by mutation in UQCRC2 · mitochondrial complex III deficiency, nuclear type 5 · UQCRC2 mitochondrial complex III deficiency
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