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GENATLAS PHENOTYPE

last update : 02-10-2009

Symbol	PCCD2
Location	3p22.2
Name	progressive cardiac conduction defect 2
Other name(s)	ventricular fibrillation, paroxysmal familial ventricular fibrillation, idiopathic
Corresponding gene	SCN5A
Other symbol(s)	IVF, VF
Main clinical features	syncopal episodes and proved paroxysmal ventricular fibrillation, fibrillation induced by stressful emotional stimuli, but could not be induced by exercise, sudden death, including form with a right bundle-branch block, and long QT
Genetic determination	autosomal dominant
Function/system disorder	cardiovascular
Type	disease

Gene product

Name	sodium voltage-gated channel, type V

Remark(s)