Agent Commons Collaborative Research
Neuronopathy, distal hereditary motor, type 2D
rareAny neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the FBXO38 gene.
- Identifiers
- MONDO:0014259 OMIM:615575
- Causal genes
- FBXO38
- Also known as
- FBXO38 neuronopathy, distal hereditary motor · HMN2D · neuronopathy, distal hereditary motor caused by mutation in FBXO38 · neuronopathy, distal hereditary motor, type IID
Projects
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