Hereditary Spastic Paraplegia 12
Disease ID: disease_node_16643
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| Dbxref | GARD:9586, ICD10CM:G11.4, MIM:604805, ORDO:100993 |
|---|---|
| Subclassof | DOID_0050736, DOID_2476 |
| Data Source | DOID |
| Synonyms | SPG12, autosomal dominant spastic paraplegia 12, autosomal dominant spastic paraplegia type 12 |
| Doid Label | hereditary spastic paraplegia 12 |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in mutation in the RTN2 gene on chromosome 19q13. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_16643 |
| Doid Id | DOID_0110765 |
| Label | Hereditary Spastic Paraplegia 12 |
- 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)