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GTR Home > Conditions/Phenotypes > Hearing loss, autosomal dominant 72

Available tests

6 tests are in the database for this condition.

Genes See tests for all associated and related genes

  • Also known as: C6orf29, CTL4, DFNA72, NG22, TPPT, hTPPT1, SLC44A4
    Summary: solute carrier family 44 member 4

Clinical features

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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.