familial hemiplegic migraine type 2
GPTKB entity
Statements (19)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
neurological disorder |
| gptkbp:associatedWith |
seizures
ataxia |
| gptkbp:diagnosedBy |
genetic testing
|
| gptkbp:firstDescribed |
1996
|
| https://www.w3.org/2000/01/rdf-schema#label |
familial hemiplegic migraine type 2
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:mutationAssociatedWith |
ATP1A2 gene
|
| gptkbp:OMIM |
602481
|
| gptkbp:prevalence |
rare
|
| gptkbp:subclassOf |
familial hemiplegic migraine
|
| gptkbp:symptom |
gptkb:migraine_with_aura
headache visual disturbances hemiparesis |
| gptkbp:treatment |
symptomatic management
|
| gptkbp:bfsParent |
gptkb:ATP1A2
|
| gptkbp:bfsLayer |
8
|