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GTR Home > Conditions/Phenotypes > Hearing loss, autosomal dominant 88

Summary

Autosomal dominant deafness-88 (DFNA88) is characterized by nonsyndromic postlingual progressive severe sensorineural hearing loss with tinnitus (Jiang et al., 2011; Huang et al., 2023). [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: DFNA88, EPHA10
    Summary: EPH receptor A10

Clinical features

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