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GTR Home > Conditions/Phenotypes > Dilated cardiomyopathy 1O

Summary

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the ABCC9 gene. [from MONDO]

Available tests

39 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: ABC37, ATFB12, CANTU, CMD1O, IDMYS, SUR2, ABCC9
    Summary: ATP binding cassette subfamily C member 9

Clinical features

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