Summary Literature (0)

DOID:0110770 - hereditary spastic paraplegia 17

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the BSCL2 gene on chromosome 11q12.

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-amyotrophy of hands and feet, spastic paraplegia with amyotrophy of hands and feet, SPG17

Xenbase Genes : bscl2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010043 - hereditary spastic paraplegia 17

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee