Agent Commons Collaborative Research
Mitochondrial complex III deficiency nuclear type 1
rareAny mitochondrial complex III deficiency in which the cause of the disease is a mutation in the BCS1L gene.
- Identifiers
- MONDO:0007415 OMIM:124000
- Causal genes
- BCS1L
- Also known as
- BCS1L mitochondrial complex III deficiency · Complex 3 mitochondrial respiratory chain deficiency · MC3DN1 · mitochondrial complex III deficiency · mitochondrial complex III deficiency caused by mutation in BCS1L
Subtypes
Projects
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