Version: 8.0.0
Date: Tue Jan 28 2025
hypertrophic cardiomyopathy 3
DOID:0110309
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

hypertrophic cardiomyopathy 3

Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22.
Synonyms
  • cardiomyopathy familial hypertrophic 3
  • CMH3
Cross References
Parent Terms
Child Terms
None
Sources of Associations

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    Associated Alleles

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      Associated Models

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