Statements (26)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
gptkb:hereditary_spastic_paraplegia |
| gptkbp:affectedStructure |
corticospinal tract
|
| gptkbp:affects |
gptkb:nervous_system
|
| gptkbp:alsoKnownAs |
gptkb:hereditary_spastic_paraplegia
familial spastic paraplegia |
| gptkbp:category |
neurological disorder
rare disease |
| gptkbp:hasOrphanetID |
ORPHA:319
|
| https://www.w3.org/2000/01/rdf-schema#label |
Strümpell-Lorrain disease
|
| gptkbp:ICD-10_code |
G11.4
|
| gptkbp:inheritance |
autosomal dominant
autosomal recessive |
| gptkbp:namedAfter |
gptkb:Adolf_Strümpell
gptkb:Maurice_Lorrain |
| gptkbp:OMIM |
182600
|
| gptkbp:onset |
childhood
adulthood |
| gptkbp:symptom |
difficulty walking
progressive spasticity of the lower limbs weakness of the lower limbs |
| gptkbp:treatment |
physical therapy
medications for spasticity |
| gptkbp:bfsParent |
gptkb:Hereditary_spastic_paraplegia
gptkb:ORPHA:447 |
| gptkbp:bfsLayer |
6
|