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hereditary spastic paraplegia 23

Go to external page http://purl.obolibrary.org/obo/DOID_0110774

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 23

Synonyms
  • Lison syndrome
  • SPG23
  • Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome
  • spastic paraplegia 23
  • spastic paraplegia with pigmentary abnormalities
database cross reference
has obo namespace

disease_ontology

id

DOID:0110774