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Dilated cardiomyopathy 1G

Synonyms
TTN-Related Dilated Cardiomyopathy

Summary

Dilated cardiomyopathy-1G (CMD1G) is an autosomal dominant disorder characterized by ventricular dilatation and systolic contractile dysfunction (Siu et al., 1999). For a general phenotypic description and a discussion of genetic heterogeneity of dilated cardiomyopathy (CMD), see CMD1A (115200). [from OMIM]

Available tests

76 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (76 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CMD1G, CMH9, CMPD4, CMYP5, EOMFC, HMERF, LGMD2J, LGMDR10, MYLK5, SALMY, TMD, TTN
    Summary: titin

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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