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GTR Home > Conditions/Phenotypes > Autosomal recessive nonsyndromic hearing loss 7

Summary

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the TMC1 gene. [from MONDO]

Available tests

26 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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