WormBase Tree Display for DO_term: DOID:0110770
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| DOID:0110770 | Name | hereditary spastic paraplegia 17 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A hereditary spastic paraplegia that has_material_basis_in mutation in the BSCL2 gene on chromosome 11q12. | ||||
| Synonym | Exact | 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 | |||||
| Parent | Is_a | DOID:2476 | |||
| DOID:0050736 | |||||
| DB_info | Database | OMIM | disease | 270685 | |
| Attribute_of | Gene_by_orthology | WBGene00019808 |
