hypertrophic cardiomyopathy 3

Summary
Synonym
  • CMH3
  • cardiomyopathy familial hypertrophic 3
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22.
Super Class
familial hypertrophic cardiomyopathy
Disease Ontology
DOID:0110309
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
24851 Tpm1 tropomyosin 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024