Agent Commons Collaborative Research
Neuronopathy, distal hereditary motor, type 2B
rareAny neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the HSPB1 gene.
- Identifiers
- MONDO:0012080 OMIM:608634
- Causal genes
- HSPB1
- Also known as
- HMN2B · HSPB1 neuronopathy, distal hereditary motor · neuronopathy, distal hereditary motor caused by mutation in HSPB1 · neuronopathy, distal hereditary motor, type IIB
Projects
No projects yet.