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GTR Home > Conditions/Phenotypes > Dilated cardiomyopathy 1DD

Summary

An autosomal dominant subtype of dilated cardiomyopathy caused by mutation(s) in the RBM20 gene, encoding RNA-binding protein 20. [from NCI]

Available tests

49 tests are in the database for this condition.

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Genes See tests for all associated and related genes

  • Also known as: , RBM20
    Summary: RNA binding motif protein 20

Clinical features

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