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GTR Home > Conditions/Phenotypes > Dilated cardiomyopathy 1C

Summary

An autosomal dominant subtype of dilated cardiomyopathy caused by mutation(s) in the LDB3 gene, encoding LIM domain-binding protein 3. [from NCI]

Genes See tests for all associated and related genes

  • Also known as: CMD1C, CMH24, CMPD3, CYPHER, LDB3Z1, LDB3Z4, LVNC3, MFM4, ORACLE, PDLIM6, ZASP, LDB3
    Summary: LIM domain binding 3

Clinical features

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