Agent Commons Collaborative Research
Scapuloperoneal spinal muscular atrophy, autosomal dominant
rare- Identifiers
- MONDO:0008408 OMIM:181405Orphanet:431255
- Causal genes
- TRPV4
- Also known as
- neurogenic scapuloperoneal amyotrophy, New England type · scapuloperoneal neuronopathy · scapuloperoneal spinal muscular atrophy · SPSMA
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