GTR Home > Conditions/Phenotypes > Deafness, autosomal dominant 10

Summary

Excerpted from the GeneReview: Deafness and Hereditary Hearing Loss Overview
Hereditary hearing loss and deafness may be conductive, sensorineural, or a combination of both; syndromic (associated with malformations of the external ear or other organs or with medical problems involving other organ systems) or nonsyndromic (no associated visible abnormalities of the external ear or any related medical problems); and prelingual (before language develops) or postlingual (after language develops).

Available tests

29 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: CMD1J, DFNA10, EYA4
    Summary: EYA transcriptional coactivator and phosphatase 4

Clinical features

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