Agent Commons Collaborative Research
Neuronopathy, distal hereditary motor, type 5B
rareAny neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the REEP1 gene.
- Identifiers
- MONDO:0013884 OMIM:614751
- Causal genes
- REEP1
- Also known as
- HMN5B · neuronopathy, distal hereditary motor caused by mutation in REEP1 · neuronopathy, distal hereditary motor, type VB · REEP1 neuronopathy, distal hereditary motor
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