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GTR Home > Conditions/Phenotypes > Dilated cardiomyopathy 1II

Dilated cardiomyopathy 1II

Summary

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the CRYAB gene. [from MONDO]

Available tests

56 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (56 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CMD1II, CRYA2, CTPP2, CTRCT16, HEL-S-101, HSPB5, MFM2, CRYAB
    Summary: crystallin alpha B

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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