familial spastic paraparesis
GPTKB entity
Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
gptkb:hereditary_spastic_paraplegia |
| gptkbp:affects |
gptkb:spinal_cord
upper motor neurons |
| gptkbp:canBeChronic |
true
|
| gptkbp:causedBy |
genetic disorder
|
| https://www.w3.org/2000/01/rdf-schema#label |
familial spastic paraparesis
|
| gptkbp:inheritance |
autosomal dominant
autosomal recessive X-linked |
| gptkbp:isProgressive |
true
|
| gptkbp:onset |
childhood
adulthood |
| gptkbp:symptom |
gait disturbance
spasticity of lower limbs progressive weakness of lower limbs |
| gptkbp:synonym |
gptkb:hereditary_spastic_paraplegia
hereditary spastic paraparesis |
| gptkbp:treatment |
physical therapy
mobility aids medications for spasticity |
| gptkbp:bfsParent |
gptkb:Hereditary_spastic_paraplegia
|
| gptkbp:bfsLayer |
6
|