Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
|
| gptkbp:abbreviation |
gptkb:SCA2
|
| gptkbp:affects |
gptkb:nervous_system
gptkb:cerebellum |
| gptkbp:alsoKnownAs |
Spinocerebellar ataxia type 2
|
| gptkbp:category |
gptkb:neurodegenerative_disease
|
| gptkbp:causedBy |
mutation in ATXN2 gene
|
| gptkbp:diagnosedBy |
genetic testing
|
| gptkbp:firstDescribed |
1990
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:OMIM |
183090
|
| gptkbp:onset |
adulthood
|
| gptkbp:prevalence |
rare
|
| gptkbp:progression |
progressive
|
| gptkbp:symptom |
gptkb:peripheral_neuropathy
tremor ataxia dysarthria slow saccadic eye movements |
| gptkbp:treatment |
supportive care
|
| gptkbp:bfsParent |
gptkb:John_Frusciante_–_The_Empyrean
|
| gptkbp:bfsLayer |
7
|
| https://www.w3.org/2000/01/rdf-schema#label |
Ataxia II
|