Hereditary Spastic Paraplegia 13
Disease ID: disease_node_16642
Connections displayed (default: 10).
Loading graph...
| Dbxref | GARD:9616, ICD10CM:G11.4, MIM:605280, ORDO:100994 |
|---|---|
| Subclassof | DOID_0050736, DOID_2476 |
| Data Source | DOID |
| Synonyms | SPG13, autosomal dominant spastic paraplegia 13 |
| Doid Label | hereditary spastic paraplegia 13 |
| Doid Description | A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 gene on chromosome 2q33. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_16642 |
| Doid Id | DOID_0110766 |
| Label | Hereditary Spastic Paraplegia 13 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Spastic Paraplegia, Hereditary(ID:disease_node_8225) (Disease)