hereditary spastic paraplegia 4 (Q2308013)

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hereditary spastic paraplegia that is characterized by slowly progressive muscle weakness and spasticity and has material basis in mutation in the SPAST gene on chromosome 2p22
  • SPG4
  • SPAST-associated HSP
  • autosomal dominant spastic paraplegia 4
  • autosomal dominant spastic paraplegia type 4
  • SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4
  • hereditary spastic paraplegia type 4
  • SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT
  • Familial Spastic Paraplegia, Autosomal Dominant, 2
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English
hereditary spastic paraplegia 4
hereditary spastic paraplegia that is characterized by slowly progressive muscle weakness and spasticity and has material basis in mutation in the SPAST gene on chromosome 2p22
  • SPG4
  • SPAST-associated HSP
  • autosomal dominant spastic paraplegia 4
  • autosomal dominant spastic paraplegia type 4
  • SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4
  • hereditary spastic paraplegia type 4
  • SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT
  • Familial Spastic Paraplegia, Autosomal Dominant, 2

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C129981
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