Term Name:	hereditary spastic paraplegia 17
Synonyms:	autosomal dominant spastic paraplegia 17, autosomal dominant spastic paraplegia type 17, dHMN5B, distal hereditary motor neuropathy type 5B, Silver spastic paraplegia syndrome, Silver syndrome, spastic paraplegia with amyotrophy of hands and feet, spastic paraplegia-amyotrophy of hands and feet, SPG17
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the BSCL2 gene on chromosome 11q12.
Ontology:	Human Disease [DOID:0110770]   ( DOID:0110770 )