Hereditary Spastic Paraplegia 23
Disease ID: disease_node_16634
Connections displayed (default: 10).
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| Dbxref | GARD:336, ICD10CM:G11.4, MIM:270750, ORDO:101003 |
|---|---|
| Subclassof | DOID_2476, DOID_0050737 |
| Data Source | DOID |
| Synonyms | Lison syndrome, SPG23, Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome, spastic paraplegia 23, spastic paraplegia with pigmentary abnormalities |
| Doid Label | hereditary spastic paraplegia 23 |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16634 |
| Doid Id | DOID_0110774 |
| Label | Hereditary Spastic Paraplegia 23 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Spastic Paraplegia, Hereditary(ID:disease_node_8225) (Disease)