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GTR Home > Conditions/Phenotypes > Dilated cardiomyopathy 1J

Dilated cardiomyopathy 1J

Synonyms
CARDIOMYOPATHY, DILATED, WITH SENSORINEURAL HEARING LOSS, AUTOSOMAL DOMINANT; EYA4-Related Dilated Cardiomyopathy
Modes of inheritance
Autosomal dominant inheritance (Orphanet)

Summary

Sensorineural deafness with dilated cardiomyopathy is an extremely rare autosomal dominant syndrome described in two families to date and characterized by moderate to severe sensorineural hearing loss manifesting during childhood, and associated with late-onset dilated cardiomyopathy that generally progresses to heart failure. [from ORDO]

Available tests

41 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (41 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CMD1J, DFNA10, EYA4
    Summary: EYA transcriptional coactivator and phosphatase 4

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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