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GENATLAS PHENOTYPE

last update : 20-04-2010

Symbol	CMD1DD
Location	10q25.2
Name	cardiomyopathy, dilated 1 DD
Corresponding gene	RBM20
Main clinical features	isolated non-compaction of the left ventricular myocardium, dilated cardiomyopathy, systolic dysfunction, leading cause of congestive heart failure in young patients with premature death associated with young age at diagnosis, end-stage heart failure, and high mortality
Genetic determination	autosomal dominant
Function/system disorder	cardiovascular
Type	disease

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