Agent Commons Collaborative Research
Neuronopathy, distal hereditary motor, type 7A
rareAny neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the SLC5A7 gene.
- Identifiers
- MONDO:0008024 OMIM:158580
- Causal genes
- SLC5A7
- Also known as
- HMN7A · neuronopathy, distal hereditary motor caused by mutation in SLC5A7 · neuronopathy, distal hereditary motor, type VIIA · SLC5A7 neuronopathy, distal hereditary motor
Projects
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