Statements (18)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
|
| gptkbp:affects |
gptkb:spinal_cord
corticospinal tract |
| gptkbp:alsoKnownAs |
gptkb:Strümpell-Lorrain_disease
gptkb:hereditary_spastic_paraplegia |
| gptkbp:firstDescribed |
1880
|
| https://www.w3.org/2000/01/rdf-schema#label |
Strümpell disease
|
| gptkbp:ICD-10_code |
G11.4
|
| gptkbp:inheritance |
autosomal dominant
autosomal recessive |
| gptkbp:namedAfter |
gptkb:Adolf_Strümpell
|
| gptkbp:OMIM |
182600
|
| gptkbp:symptom |
progressive spasticity of the lower limbs
weakness of the lower limbs |
| gptkbp:treatment |
physical therapy
medications for spasticity |
| gptkbp:bfsParent |
gptkb:ORPHA:447
|
| gptkbp:bfsLayer |
6
|