hereditary spastic paraplegia 17 (Q32142660)

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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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Language Label Description Also known as
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

Statements

instance of
rare disease
0 references
class of disease
0 references

Identifiers

Mondo ID
MONDO_0010043
0 references
 
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