WormBase Tree Display for DO_term: DOID:0110774
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| DOID:0110774 | Name | hereditary spastic paraplegia 23 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32. | ||||
| Synonym | Exact | Lison syndrome | |||
| SPG23 | |||||
| Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome | |||||
| spastic paraplegia 23 | |||||
| spastic paraplegia with pigmentary abnormalities | |||||
| Parent | Is_a | DOID:2476 | |||
| DOID:0050737 | |||||
| DB_info | Database | OMIM | disease | 270750 |
