Variants
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Dilated cardiomyopathy 1O

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Description

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the ABCC9 gene.

MONDO

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

401

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Genes

External Links

  • OMIM

    608569

  • Orphanet
  • HPO
  • Medgen

    C1837839

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