Parkinson Disease, Hereditary
GPTKB entity
Statements (27)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
neurodegenerative disease
genetic disorder |
| gptkbp:affects |
central nervous system
|
| gptkbp:associatedWith |
gptkb:LRRK2
gptkb:SNCA gptkb:DJ-1 gptkb:PARK2 gptkb:PINK1 |
| gptkbp:causedBy |
genetic disorder
|
| gptkbp:hasOrphanetID |
ORPHA:411602
|
| https://www.w3.org/2000/01/rdf-schema#label |
Parkinson Disease, Hereditary
|
| gptkbp:ICD-10_code |
gptkb:G20
|
| gptkbp:inheritance |
autosomal dominant
autosomal recessive |
| gptkbp:MeSH_ID |
D010300
|
| gptkbp:OMIM |
168600
|
| gptkbp:onset |
adult
juvenile |
| gptkbp:symptom |
bradykinesia
postural instability rigidity tremor |
| gptkbp:treatment |
gptkb:levodopa
deep brain stimulation dopamine agonists |
| gptkbp:bfsParent |
gptkb:D010141
|
| gptkbp:bfsLayer |
7
|