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GTR Home > Conditions/Phenotypes > Hypertrophic cardiomyopathy 13

Hypertrophic cardiomyopathy 13

Synonyms
Familial hypertrophic cardiomyopathy 13; TNNC1-Related Familial Hypertrophic Cardiomyopathy

Summary

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNC1 gene. [from MONDO]

Available tests

45 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (45 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CMD1Z, CMH13, TN-C, TNC, TNNC, TNNC1
    Summary: troponin C1, slow skeletal and cardiac type

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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