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GTR Home > Conditions/Phenotypes > Autosomal dominant nonsyndromic hearing loss 12

Summary

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

Genes See tests for all associated and related genes

  • Also known as: DFNA12, DFNA8, DFNB21, TECTA
    Summary: tectorin alpha

Clinical features

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