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GENATLAS PHENOTYPE

last update : 07-01-2014

Symbol	CMD1O
Location	12p12.1
Name	cardiomyopathy, dilated 1O
Corresponding gene	ABCC9
Main clinical features	with ventricular tachycardia, severely dilated with compromised contractile function and rythm disturbances
Genetic determination	autosomal dominant
Function/system disorder	cardiovascular
Type	disease

Gene product

Name	ATP-binding cassette, sub-family C (CFTR/MRP), member 9, catalytic K atp channel

Remark(s)