Statements (24)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:neurological_disorder
gptkb:hereditary_spastic_paraplegia |
| gptkbp:affects |
corticospinal tract
|
| gptkbp:alternativeName |
gptkb:hereditary_spastic_paraplegia
gptkb:familial_spastic_paraparesis |
| gptkbp:causedBy |
gptkb:genetic_disorder
|
| gptkbp:diagnosedBy |
gptkb:neurological_examination
genetic testing |
| gptkbp:ICD-10_code |
G11.4
|
| gptkbp:inheritance |
autosomal dominant
autosomal recessive X-linked |
| gptkbp:onset |
childhood
adulthood |
| gptkbp:subspecies |
spastic paraplegia
|
| gptkbp:symptom |
spasticity
difficulty walking progressive weakness of lower limbs |
| gptkbp:treatment |
physical therapy
mobility aids medications for spasticity |
| gptkbp:bfsParent |
gptkb:ORPHA:447
|
| gptkbp:bfsLayer |
6
|
| https://www.w3.org/2000/01/rdf-schema#label |
Familial spastic paraplegia
|