Familial atrial fibrillation
GPTKB entity
Statements (54)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:arrhythmia
genetic disorder |
| gptkbp:affects |
heart
|
| gptkbp:associatedWith |
gptkb:RYR2
gptkb:KCNE2 gptkb:KCNJ2 gptkb:PRKAG2 gptkb:ANK2 gptkb:NPPA gptkb:CAMK2D gptkb:CASQ2 gptkb:GATA4 gptkb:GATA6 gptkb:GJA1 gptkb:GJA5 gptkb:GNB2 gptkb:HCN4 gptkb:KCNA5 gptkb:KCNJ5 gptkb:KCNJ8 gptkb:MYL4 gptkb:NUP155 gptkb:PITX2 gptkb:RPL3L gptkb:SCN10A gptkb:SCN1B gptkb:SCN2B gptkb:SCN3B gptkb:SYNE2 gptkb:TBX5 gptkb:ZFHX3 gptkb:LMNA gptkb:KCNQ1 gptkb:TTN gptkb:KCNH2 gptkb:SCN5A |
| gptkbp:cause |
heart failure
stroke |
| gptkbp:causedBy |
genetic disorder
|
| gptkbp:hasOrphanetID |
ORPHA:98856
|
| https://www.w3.org/2000/01/rdf-schema#label |
Familial atrial fibrillation
|
| gptkbp:ICD-10_code |
I48
|
| gptkbp:isInheritedAs |
autosomal dominant
|
| gptkbp:OMIM |
608583
|
| gptkbp:riskFactor |
family history
|
| gptkbp:symptom |
dizziness
shortness of breath palpitations irregular heartbeat |
| gptkbp:treatment |
catheter ablation
anticoagulants antiarrhythmic drugs |
| gptkbp:bfsParent |
gptkb:HGNC:6407
|
| gptkbp:bfsLayer |
6
|