Hereditary Spastic Paraplegia 42
Disease ID: disease_node_16685
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:G11.4, MIM:612539, ORDO:171863 |
|---|---|
| Subclassof | DOID_0050736, DOID_2476 |
| Data Source | DOID |
| Synonyms | SPG42, autosomal dominant spastic paraplegia 42, autosomal dominant spastic paraplegia type 42 |
| Doid Label | hereditary spastic paraplegia 42 |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in mutation in the SLC33A1 gene on chromosome 3q25.31. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_16685 |
| Doid Id | DOID_0110794 |
| Label | Hereditary Spastic Paraplegia 42 |
- Outgoing r'ship
SUBCLASS_OFto/from Spastic Paraplegia, Hereditary(ID:disease_node_8225) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)