Terminology Service for NFDI4Health

hereditary spastic paraplegia 17

Go to external page http://purl.obolibrary.org/obo/DOID_0110770


A hereditary spastic paraplegia that has_material_basis_in mutation in the BSCL2 gene on chromosome 11q12. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 17

Synonyms
  • SPG17
  • Silver spastic paraplegia syndrome
  • Silver syndrome
  • autosomal dominant spastic paraplegia 17
  • autosomal dominant spastic paraplegia type 17
  • dHMN5B
  • distal hereditary motor neuropathy type 5B
  • spastic paraplegia with amyotrophy of hands and feet
  • spastic paraplegia-amyotrophy of hands and feet
database cross reference
has obo namespace

disease_ontology

id

DOID:0110770