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Hypertrophic cardiomyopathy 10

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Description

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL2 gene.

MONDO

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

160

SEE THE VARIANTS →

Genes

  • MYL2

External Links

  • OMIM

    608758

  • Orphanet
  • HPO
  • Medgen

    C1834460

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