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GTR Home > Conditions/Phenotypes > Hypertrophic cardiomyopathy 12

Hypertrophic cardiomyopathy 12

Synonyms
Familial hypertrophic cardiomyopathy 12

Summary

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the CSRP3 gene. [from MONDO]

Available tests

51 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (51 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CLP, CMD1M, CMH12, CRP3, LMO4, MLP, CSRP3
    Summary: cysteine and glycine rich protein 3

Clinical features

Help
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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