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GTR Home > Conditions/Phenotypes > Autosomal recessive nonsyndromic hearing loss 8


An autosomal recessive nonsyndromic deafness that has material basis in mutation in the TMPRSS3 gene on chromosome 21q22. [from MONDO]

Available tests

23 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: DFNB10, DFNB8, ECHOS1, TADG12, TMPRSS3
    Summary: transmembrane serine protease 3

Clinical features


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