Hereditary Spastic Paraplegia 41
Disease ID: disease_node_16686
Connections displayed (default: 10).
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| Dbxref | ICD10CM:G11.4, MIM:613364, ORDO:320355 |
|---|---|
| Subclassof | DOID_0050736, DOID_2476 |
| Data Source | DOID |
| Synonyms | SPG41, autosomal dominant spastic paraplegia 41, autosomal dominant spastic paraplegia type 41 |
| Doid Label | hereditary spastic paraplegia 41 |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_16686 |
| Doid Id | DOID_0110793 |
| Label | Hereditary Spastic Paraplegia 41 |
- 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)