Variants
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Hypertrophic cardiomyopathy 11

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Description

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the ACTC1 gene.

MONDO

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

217

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Genes

External Links

  • OMIM

    612098

  • Orphanet
  • HPO
  • Medgen

    C2677506

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