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GTR Home > Conditions/Phenotypes > Dilated cardiomyopathy 1HH

Summary

An autosomal dominant subtype of dilated cardiomyopathy caused by mutation(s) in the BAG3 gene, encoding BAG family molecular chaperone regulator 3. [from NCI]

Available tests

53 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: BAG-3, BIS, CAIR-1, MFM6, BAG3
    Summary: BAG cochaperone 3

Clinical features

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