Home Page |
References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 03-11-2010 |
Symbol | ATFB12 |
Location | 11q24.1 |
Name | atrial fibrillation, familial, 12 |
Corresponding gene | SCN3B |
Main clinical features | cardiac disorder characterized by supraventricular tachyarrhythmia due to uncoordinated atrial activation, a rapid atrial rate of 150–300 beats/min, absence of P waves, presence of rapid oscillations or fibrillatory waves (f waves), and inconsistent R-R intervals on electrocardiograms (ECG) |
Genetic determination | not applicable |
Function/system disorder | cardiovascular |
Type | disease |
Remark(s) |
|