(Q4664694)

English

hereditary spastic paraplegia 23

hereditary spastic paraplegia that has material basis in variation in the chromosome region 1q24-q32

  • spastic paraplegia type 23
  • Lison syndrome
  • SPG23
  • spastic paraplegia with pigmentary abnormalities
  • Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome
  • spastic paraplegia 23
  • SPASTIC PARAPLEGIA 23; SPG23
  • Autosomal recessive spastic paraplegia type 23
  • Spastic Paraparesis, Vitiligo, Premature Graying, Characteristic Facies
  • hereditary spastic paraplegia type 23
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