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GTR Home > Conditions/Phenotypes > Hearing loss, autosomal dominant 86

Summary

Autosomal dominant deafness-86 (DFNA86) is characterized by late-onset progressive hearing loss through p53 (TP53; 191170)-mediated hair cell apoptosis (Zhang et al., 2020). [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: DFNA86, HPR1, P84, P84N5, THOC1
    Summary: THO complex subunit 1

Clinical features

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