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Dilated cardiomyopathy 1BB

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Description

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the DSG2 gene.

MONDO

  • Mode of Inheritance

    VARIANTS

    5

    SEE THE VARIANTS →

    Genes

    • DSG2

    External Links

    • OMIM

      612877

    • Orphanet
    • HPO
    • Medgen

      C2752072

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