Hereditary Spastic Paraplegia 2
Disease ID: disease_node_16635
Connections displayed (default: 10).
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| Dbxref | GARD:4923, ICD10CM:G11.4, MIM:312920, ORDO:99015 |
|---|---|
| Subclassof | DOID_0080012, DOID_2476 |
| Data Source | DOID |
| Synonyms | SPG2, X-linked spastic paraplegia 2, spastic paraplegia type 2 |
| Doid Label | hereditary spastic paraplegia 2 |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2. |
| Has Material Basis In | GENO_0000149 |
| Disease Node Id | disease_node_16635 |
| Doid Id | DOID_0110773 |
| Label | Hereditary Spastic Paraplegia 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Spastic Paraplegia, Hereditary(ID:disease_node_8225) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from X-Linked Recessive Disease(ID:disease_node_13254) (Disease)