U.S. flag

An official website of the United States government

GTR Home > Conditions/Phenotypes > Autosomal dominant nonsyndromic hearing loss 25

Autosomal dominant nonsyndromic hearing loss 25

Synonyms
DFNA25 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal dominant 25

Summary

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the SLC17A8 gene. [from MONDO]

Available tests

22 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (22 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: DFNA25, VGLUT3, SLC17A8
    Summary: solute carrier family 17 member 8

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.