Statements (19)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:arrhythmia
genetic disorder |
| gptkbp:affects |
cardiac repolarization
|
| gptkbp:associatedWith |
gptkb:KCNH2
|
| gptkbp:firstDescribed |
2000
|
| https://www.w3.org/2000/01/rdf-schema#label |
Short QT syndrome 1
|
| gptkbp:ICD-10_code |
I45.81
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:mutationAssociatedWith |
gptkb:KCNH2_gene
|
| gptkbp:OMIM |
609620
|
| gptkbp:prevalence |
rare
|
| gptkbp:riskFactor |
family history of sudden cardiac death
|
| gptkbp:symptom |
sudden cardiac death
syncope shortened QT interval |
| gptkbp:treatment |
gptkb:implantable_cardioverter-defibrillator
quinidine |
| gptkbp:bfsParent |
gptkb:O60500
|
| gptkbp:bfsLayer |
7
|