U.S. flag

An official website of the United States government

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

48 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (48 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

Help
Imported from Human Phenotype Ontology (HPO)

Show allHide all

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.