hereditary spastic paraplegia 11

Summary
Synonym
  • HSP-TCC
  • Nakamura-Osame syndrome
  • SPG11
  • autosomal recessive spastic paraplegia 11
  • autosomal recessive spastic paraplegia complicated with thin corpus callosum
  • autosomal recessive spastic paraplegia type 11
  • autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum
  • spastic paraplegia-intellectual disability-thin corpus callosum syndrome
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21.
Super Class
autosomal recessive disease hereditary spastic paraplegia
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
80208 SPG11 SPG11 vesicle trafficking associated, spatacsin

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024