(Q32142846)
English
hereditary spastic paraplegia 31
30 years). In some cases, it can present as a complex phenotype with additional associated manifestations including peripheral neuropathy, bulbar palsy (with dysarthria and dysphagia), distal amyotrophy, and impaired distal vibration sense.
- autosomal dominant spastic paraplegia type 31
- autosomal dominant spastic paraplegia 31
- SPG31
- hereditary spastic paraplegia type 31
- SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31
- SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT
- Spastic paraplegia 31
Statements
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C189921
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Identifiers
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Sitelinks
Wikipedia(1 entry)
- enwiki Spastic paraplegia 31