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GTR Home > Conditions/Phenotypes > Autosomal dominant nonsyndromic hearing loss 20

Summary

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the ACTG1 gene. [from MONDO]

Genes See tests for all associated and related genes

  • Also known as: ACT, ACTG, DFNA20, DFNA26, HEL-176, ACTG1
    Summary: actin gamma 1

Clinical features

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