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GENATLAS PHENOTYPE
last update : 06-01-2014
Symbol CMD1W
Location 10q22.2
Name cardiomyopathy, dilated 1W
Corresponding gene VCL
Other symbol(s) CMD1L, CMD15, CMD1N
Main clinical features
  • adult-onset, in any cases associated with juvenile-onset neurosensory hearing loss
  • Genetic determination autosomal dominant
    Function/system disorder cardiovascular
    Type disease
    Gene product
    Name vinculin
    Remark(s)