Search Ontology:
Human Disease

hereditary spastic paraplegia 23

Term ID
DOID:0110774
Synonyms
  • Lison syndrome
  • Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome
  • spastic paraplegia 23
  • spastic paraplegia with pigmentary abnormalities
  • SPG23
Definition
A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32. https://www.ncbi.nlm.nih.gov/pubmed/14681889
References
Ontology
Human Disease   ( DOID:0110774 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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