hereditary spastic paraplegia 23

Summary
Synonym
  • Lison syndrome
  • SPG23
  • Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome
  • spastic paraplegia 23
  • spastic paraplegia with pigmentary abnormalities
Definition
A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32.
Super Class
autosomal recessive disease hereditary spastic paraplegia
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
25778 DSTYK dual serine/threonine and tyrosine protein kinase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024