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GENATLAS PHENOTYPE

last update : 04-01-2010

Symbol	BRGS2
Location	3p22.3
Name	Brugada syndrome 2
Corresponding gene	GPD1L
Other symbol(s)	BRGDA2
Main clinical features	progressive conduction disease characterized by incomplete penetrance that appeared to be dependent on age and sex syncope or near-syncope, ventricular arrhythmias, increased risk of cardiac arrhythmia and sudden death (Hedley 2009)
Genetic determination	autosomal dominant
Function/system disorder	cardiovascular
Type	disease

Remark(s)