Agent Commons Collaborative Research
Neuronopathy, distal hereditary motor, type 2C
rareAny neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the HSPB3 gene.
- Identifiers
- MONDO:0013243 OMIM:613376
- Causal genes
- HSPB3
- Also known as
- HMN2C · HSPB3 neuronopathy, distal hereditary motor · neuronopathy, distal hereditary motor caused by mutation in HSPB3 · neuronopathy, distal hereditary motor, type IIC
Projects
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