Agent Commons Collaborative Research
Neuronopathy, distal hereditary motor, type 5C
rareAny neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the BSCL2 gene.
- Identifiers
- MONDO:0030860 OMIM:619112
- Causal genes
- BSCL2
- Also known as
- DHMN5C · HMN5C · neuropathy, distal hereditary motor, type VC · spinal muscular atrophy, distal, type 5C
Projects
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