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GTR Home > Conditions/Phenotypes > Autosomal dominant nonsyndromic hearing loss 40

Summary

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

Genes See tests for all associated and related genes

  • Also known as: DFNA40, THBP, CRYM
    Summary: crystallin mu

Clinical features

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