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GTR Home > Conditions/Phenotypes > Hypertrophic cardiomyopathy 8

Hypertrophic cardiomyopathy 8

Synonyms
CARDIOMYOPATHY, HYPERTROPHIC, MID-LEFT VENTRICULAR CHAMBER TYPE, 1; Familial hypertrophic cardiomyopathy 8; MYL3-Related Familial Hypertrophic Cardiomyopathy

Summary

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL3 gene. [from MONDO]

Available tests

47 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (47 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CMH8, MLC-lV/sb, MLC1SB, MLC1V, VLC1, VLCl, MYL3
    Summary: myosin light chain 3

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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