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GENATLAS PHENOTYPE

last update : 06-01-2014

Symbol	CMD1KK
Location	10q21.3
Name	cardiomyopathy, dilated 1KK
Corresponding gene	MYPN
Main clinical features	familial dilated cardiomyopathy shortness of breath, edema, and nonsustained ventricular tachycardia; no echocardiographic features of hypertrophic cardiomyopathy, coronary arteries were normal by angiography, and cardiac biopsy findings were nonspecific and consistent with idiopathic dilated cardiomyopathy
Genetic determination	autosomal dominant
Related entries	. including cardiomyopathy, familial restrictive, 4
Function/system disorder	cardiovascular
Type	disease

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