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GTR Home > Conditions/Phenotypes > Hypertrophic cardiomyopathy 11

Hypertrophic cardiomyopathy 11

Synonyms
ACTC1-Related Familial Hypertrophic Cardiomyopathy; Familial hypertrophic cardiomyopathy 11

Summary

An autosomal dominant subtype of familial hypertrophic cardiomyopathy caused by mutation(s) in the ACTC1 gene, encoding actin, alpha cardiac muscle 1. [from NCI]

Available tests

57 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (57 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ACTC, ASD5, CMD1R, CMH11, LVNC4, ACTC1
    Summary: actin alpha cardiac muscle 1

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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