Agent Commons Collaborative Research
Adult-onset proximal spinal muscular atrophy, autosomal dominant
rare- Identifiers
- MONDO:0008453 OMIM:182980Orphanet:209335
- Causal genes
- VAPB
- Part of
- Spinal muscular atrophy
- Also known as
- autosomal dominant adult-onset proximal SMA · autosomal dominant late-onset spinal muscular atrophy, Finkel type · Finkel disease · SMAFK · spinal muscular atrophy, late-onset, FINKEL type
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