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GTR Home > Conditions/Phenotypes > Dilated cardiomyopathy 1I

Summary

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the DES gene. [from MONDO]

Genes See tests for all associated and related genes

  • Also known as: CDCD3, CSM1, CSM2, LGMD1D, LGMD1E, LGMD2R, DES
    Summary: desmin

Clinical features

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