Variants
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Dilated cardiomyopathy 1P

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Description

An autosomal dominant sub-type of dilated cardiomyopathy caused by mutation(s) in the PLN gene, encoding cardiac phospholamban.

NCI

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

54

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Genes

External Links

  • OMIM

    609909

  • Orphanet
  • HPO
  • Medgen

    C1835928

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