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GTR Home > Conditions/Phenotypes > Dilated cardiomyopathy 1CC

Summary

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

Available tests

40 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: CMH20, NELIN, NEXN
    Summary: nexilin F-actin binding protein

Clinical features

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