OBO ID: DOID:0110774
Term Name: hereditary spastic paraplegia 23 Search Ontology:
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)
OTHER hereditary spastic paraplegia 23 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DSTYK Spastic paraplegia 23 270750
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None