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GENATLAS PHENOTYPE

last update : 28/12/06

Symbol	SQT1
Location	7q36.1
Name	short QT syndrome-1
Corresponding gene	KCNH2
Main clinical features	idiopathic persistently short QT interval, associated with several episodes of paroxysmal atrial fibrillation, predisposing patients to life-threatening arrhythmias
Genetic determination	autosomal dominant
Function/system disorder	cardiovascular
Type	disease

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