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

Autosomal dominant nonsyndromic hearing loss 11

Synonyms
DFNA11 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal dominant 11

Summary

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.

Clinical tests (50 available)

Molecular Genetics 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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Imported from Human Phenotype Ontology (HPO)

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