Hereditary Spastic Paraplegia 57
Disease ID: disease_node_16662
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:G11.4, MIM:615658, ORDO:431329 |
|---|---|
| Subclassof | DOID_2476, DOID_0050737 |
| Data Source | DOID |
| Synonyms | SPG57, autosomal recessive spastic paraplegia 57, autosomal recessive spastic paraplegia type 57 |
| Doid Label | hereditary spastic paraplegia 57 |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in mutation in the TFG gene on chromosome 3q12. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16662 |
| Doid Id | DOID_0110809 |
| Label | Hereditary Spastic Paraplegia 57 |
- 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)