hereditary spastic paraplegia 17
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
hereditary spastic paraplegia 17
- 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
disease_ontology
DOID:0110770