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GTR Home > Conditions/Phenotypes > Autosomal recessive nonsyndromic hearing loss 79

Autosomal recessive nonsyndromic hearing loss 79

Synonyms
DFNB79 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal recessive 79

Summary

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

Available tests

19 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (19 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: C9orf75, DFNB79, TPRN
    Summary: taperin

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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