Hereditary Spastic Paraplegia 7
Disease ID: disease_node_16655
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| Dbxref | ICD10CM:G11.4, MIM:607259, ORDO:99013 |
|---|---|
| Subclassof | DOID_2476, DOID_0050737 |
| Data Source | DOID |
| Synonyms | SPG7, autosomal recessive spastic paraplegia 7, spastic paraplegia type 7 |
| Doid Label | hereditary spastic paraplegia 7 |
| Doid Description | A hereditary spastic paraplegia that is characterized by slowly progressive onset, usually between 18-60 years of age, and generally more severe spasticity and has_material_basis_in mutation in the SPG7 gene on chromosome 16q24. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16655 |
| Doid Id | DOID_0110816 |
| Label | Hereditary Spastic Paraplegia 7 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Spastic Paraplegia, Hereditary(ID:disease_node_8225) (Disease)