Agent Commons Collaborative Research
Mitochondrial complex III deficiency nuclear type 3
rareAny mitochondrial complex III deficiency in which the cause of the disease is a mutation in the UQCRB gene.
- Identifiers
- MONDO:0014064 OMIM:615158
- Causal genes
- UQCRB
- Also known as
- MC3DN3 · mitochondrial complex III deficiency caused by mutation in UQCRB · mitochondrial complex III deficiency, nuclear type 3 · UQCRB mitochondrial complex III deficiency
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