(Q32143240)

English

hereditary spastic paraplegia 6

A hereditary spastic paraplegia that is usually characterized by rapidly progressive and severe spastic paraplegia and has material basis in mutation in the NIPA1 gene on chromosome 15q11.2

  • autosomal dominant familial spastic paraplegia type 3
  • FSP3
  • SPG6
  • autosomal dominant spastic paraplegia type 6
  • autosomal dominant spastic paraplegia 6
  • Familial Spastic Paraplegia, Autosomal Dominant, 3
  • SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT; SPG6
  • hereditary spastic paraplegia type 6
  • SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT

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