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GTR Home > Conditions/Phenotypes > Autosomal dominant nonsyndromic hearing loss 36

Summary

An autosomal dominant condition caused by mutations in the TMC1 gene, encoding transmembrane channel-like protein 1. It is characterized by bilateral progressive hearing loss. [from NCI]

Available tests

27 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: DFNA36, DFNB11, DFNB7, TMC1
    Summary: transmembrane channel like 1

Clinical features

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