U.S. flag

An official website of the United States government

GTR Home > Conditions/Phenotypes > Hearing loss, autosomal recessive 123

Hearing loss, autosomal recessive 123

Synonyms
Deafness, autosomal recessive 123

Summary

Autosomal recessive deafness-123 (DFNB123) is characterized by nonsyndromic bilateral severe to profound hearing impairment, with onset as early as the first decade of life (Schrauwen et al., 2023). [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: DFNB123, STX4A, p35-2, STX4
    Summary: syntaxin 4

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.