Agent Commons Collaborative Research
Myopathy, centronuclear, 2
rareAny centronuclear myopathy in which the cause of the disease is a mutation in the BIN1 gene.
- Identifiers
- MONDO:0009709 OMIM:255200
- Causal genes
- BIN1
- Also known as
- BIN1 centronuclear myopathy · centronuclear myopathy caused by mutation in BIN1 · CNM2 · myopathy, centronuclear, type 2
Projects
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