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GTR Home > Conditions/Phenotypes > Dilated cardiomyopathy 1P

Summary

An autosomal dominant subtype of dilated cardiomyopathy caused by mutation(s) in the PLN gene, encoding cardiac phospholamban. [from NCI]

Available tests

64 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: CMD1P, CMH18, PLB, PLN
    Summary: phospholamban

Clinical features

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