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Disease Ontology Browser
hereditary spastic paraplegia 17 (DOID:0110770)
Alliance: disease page
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
Alt IDs: OMIM:270685, ICD10CM:G11.4, ORDO:100998
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the BSCL2 gene on chromosome 11q12.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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MGI 6.14
The Jackson Laboratory