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Hypertrophic cardiomyopathy 3

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Description

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TPM1 gene.

MONDO

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

42

SEE THE VARIANTS →

Genes

  • TPM1

External Links

  • OMIM

    115196

  • Orphanet
  • HPO
  • Medgen

    C1861863

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