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References OMIM Gene GeneReviews HGMD HGNC
last update : 21/10/2008
Symbol CMD1M
Location 11p15.1
Name cardiomyopathy, dilated 1M
Corresponding gene CSRP3
Main clinical features
  • chamber dilation, thin ventricular walls, decreased contractility and impaired relaxation
  • also hypertrophic cardiomyopathy, pronounced hypertrophy with an onset of symptoms in young adulthood, associated or not with typical myofibrillar myopathy
  • Genetic determination
    Function/system disorder cardiovascular
    Type disease
    Gene product
    Name cysteine and glycine-rich protein 3 (cardiac LIM protein)