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GTR Home > Conditions/Phenotypes > Hypertrophic cardiomyopathy 14

Hypertrophic cardiomyopathy 14

Synonyms
Familial hypertrophic cardiomyopathy 14

Summary

An autosomal dominant subtype of familial hypertrophic cardiomyopathy caused by mutation(s) in the MYH6 gene, encoding myosin-6. [from NCI]

Available tests

40 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (40 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ASD3, CMD1EE, CMH14, MYHC, MYHCA, SSS3, alpha-MHC, MYH6
    Summary: myosin heavy chain 6

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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Reviews

Clinical resources

Practice guidelines

  • EuroGenetest, 2011
    Clinical utility gene card for: hypertrophic cardiomyopathy (type 1-14).

Molecular resources

Consumer resources

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