autosomal dominant Parkinson's disease
GPTKB entity
Statements (27)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
form of Parkinson's disease |
| gptkbp:affects |
gptkb:nervous_system
|
| gptkbp:associatedWith |
gptkb:LRRK2
gptkb:SNCA gptkb:GBA VPS35 |
| gptkbp:diseaseCategory |
neurodegenerative disease
|
| gptkbp:firstDescribed |
late 20th century
|
| gptkbp:frequency |
rare
|
| https://www.w3.org/2000/01/rdf-schema#label |
autosomal dominant Parkinson's disease
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:OMIM |
607060
168601 614203 |
| gptkbp:onset |
adult
late-onset |
| gptkbp:parent |
gptkb:Parkinson's_disease
|
| gptkbp:symptom |
bradykinesia
postural instability rigidity tremor |
| gptkbp:treatment |
gptkb:levodopa
deep brain stimulation dopamine agonists |
| gptkbp:bfsParent |
gptkb:SNCA_gene_mutation
|
| gptkbp:bfsLayer |
7
|