WormBase Tree Display for DO_term: DOID:2476
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| DOID:2476 | Name | hereditary spastic paraplegia | |
|---|---|---|---|
| Status | Valid | ||
| Definition | A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs. | ||
| Comment | Xref MGI. | ||
| Synonym | Exact | French settlement disease | |
| Strumpell-Lorrain disease | |||
| familial spastic paraplegia | |||
| hereditary spastic paraparesis | |||
| Parent | Is_a | DOID:607 | |
| Child | Is (83) | ||
| Disease_model_annotation | WBDOannot00000106 | ||
| WBDOannot00000234 | |||
| WBDOannot00000383 | |||
| Attribute_of | Gene_by_biology | WBGene00000542 | |
| WBGene00016045 | |||
| WBGene00021820 | |||
| Gene_by_orthology | WBGene00002025 | ||
| WBGene00006831 | |||
| WBGene00011938 | |||
| WBGene00019808 | |||
| WBGene00021564 | |||
| Disease_model_variation | WBVar00249713 |
