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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

21 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (21 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

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Imported from Human Phenotype Ontology (HPO)

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