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GTR Home > Conditions/Phenotypes > Autosomal dominant nonsyndromic hearing loss 11


Autosomal dominant deafness-11 is a nonsyndromic form of progressive neurosensory hearing loss with postlingual onset. Some affected individuals have mild vestibular symptoms (summary by Sun et al., 2011). [from OMIM]

Available tests

50 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: DFNA11, DFNB2, MYOVIIA, MYU7A, NSRD2, USH1B, MYO7A
    Summary: myosin VIIA

Clinical features


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