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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