(Q32142660)
English
hereditary spastic paraplegia 17
hereditary spastic paraplegia that has material basis in mutation in the BSCL2 gene on chromosome 11q12
- dHMN5B
- Silver spastic paraplegia syndrome
- spastic paraplegia-amyotrophy of hands and feet
- spastic paraplegia with amyotrophy of hands and feet
- autosomal dominant spastic paraplegia type 17
- distal hereditary motor neuropathy type 5B
- SPG17
- autosomal dominant spastic paraplegia 17
- Silver syndrome
- SPASTIC PARAPLEGIA 17, AUTOSOMAL DOMINANT
- SPASTIC PARAPLEGIA 17, AUTOSOMAL DOMINANT; SPG17
- hereditary spastic paraplegia type 17
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