Hereditary Spastic Paraplegia 6
Disease ID: disease_node_16660
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:G11.4, MIM:600363, ORDO:100988 |
|---|---|
| Subclassof | DOID_0050736, DOID_2476 |
| Data Source | DOID |
| Synonyms | FSP3, SPG6, autosomal dominant familial spastic paraplegia type 3, autosomal dominant spastic paraplegia 6, autosomal dominant spastic paraplegia type 6 |
| Doid Label | hereditary spastic paraplegia 6 |
| Doid Description | A hereditary spastic paraplegia that is usually characterized by rapidly progressive and severe spastic paraplegia and has_material_basis_in mutation in the NIPA1 gene on chromosome 15q11.2. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_16660 |
| Doid Id | DOID_0110811 |
| Label | Hereditary Spastic Paraplegia 6 |
- 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)