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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: 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,
Xenbase Genes
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bscl2
| MONDO:0010043 - hereditary spastic paraplegia 17 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee