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References OMIM Gene GeneReviews HGMD HGNC
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