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GENATLAS PHENOTYPE

last update : 8/04/2006

Symbol	CMD1E
Location	3p22.2
Name	cardiomyopathy, dilated 1E
Corresponding gene	SCN5A
Other symbol(s)	DCM2, CDCD2, CMPD2
Main clinical features	sinus node dysfunction and conduction defect
Genetic determination	autosomal dominant
Function/system disorder	cardiovascular
Type	disease

Remark(s)