Hereditary Spastic Paraplegia 30
Disease ID: disease_node_16616
Connections displayed (default: 10).
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| Dbxref | ICD10CM:G11.4, MIM:610357, ORDO:101010 |
|---|---|
| Subclassof | DOID_2476, DOID_0050739 |
| Data Source | DOID |
| Synonyms | SPG30, autosomal spastic paraplegia type 30, autosomal dominant spastic paraplegia 30, autosomal recessive spastic paraplegia 30 |
| Doid Label | hereditary spastic paraplegia 30 |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF1A gene on chromosome 2q37. |
| Has Material Basis In | GENO_0000934 |
| Disease Node Id | disease_node_16616 |
| Doid Id | DOID_0110781 |
| Label | Hereditary Spastic Paraplegia 30 |
- Outgoing r'ship
SUBCLASS_OFto/from Spastic Paraplegia, Hereditary(ID:disease_node_8225) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Genetic Disease(ID:disease_node_15586) (Disease)