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GTR Home > Conditions/Phenotypes > Autosomal dominant nonsyndromic hearing loss 4B

Autosomal dominant nonsyndromic hearing loss 4B

Synonyms
Deafness, autosomal dominant 4b

Summary

Autosomal dominant deafness-4B is a form of nonsyndromic progressive sensorineural hearing loss with postlingual onset (summary by Wang et al., 2015) [from OMIM]

Available tests

18 tests are in the database for this condition.

Clinical tests (18 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CEAL2, DFNA4B, DFNB113, CEACAM16
    Summary: CEA cell adhesion molecule 16, tectorial membrane component

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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