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

Autosomal dominant nonsyndromic hearing loss 36

Synonyms
DFNA36 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal dominant 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

24 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (24 available)

Molecular Genetics 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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Imported from Human Phenotype Ontology (HPO)

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