Variants
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Primary familial dilated cardiomyopathy

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Description

A a genetic form of heart disease that occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of the heart, causing the open area of the chamber to become enlarged (dilated). As a result, the heart is unable to pump blood as efficiently as usual. To compensate, the heart attempts to increase the amount of blood being pumped through the heart, leading to further thinning and weakening of the cardiac muscle. Over time, this condition results in heart failure.

MONDO

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

120

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Genes

External Links

  • OMIM

    600884

  • Orphanet

    217607

  • HPO
  • Medgen

    C0340427

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