Hereditary Spastic Paraplegia 29
Disease ID: disease_node_16628
Connections displayed (default: 10).
Loading graph...
| Dbxref | GARD:9729, ICD10CM:G11.4, MIM:609727, ORDO:101009 |
|---|---|
| Subclassof | DOID_0050736, DOID_2476 |
| Data Source | DOID |
| Synonyms | SPG29, autosomal dominant spastic paraplegia 29 |
| Doid Label | hereditary spastic paraplegia 29 |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1p31.1-p21.1. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_16628 |
| Doid Id | DOID_0110780 |
| Label | Hereditary Spastic Paraplegia 29 |
- 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)