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GTR Home > Conditions/Phenotypes > Autosomal dominant nonsyndromic hearing loss 4A

Summary

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYH14 gene. [from MONDO]

Available tests

22 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: DFNA4, DFNA4A, FP17425, MHC16, MYH17, NMHC II-C, NMHC-II-C, PNMHH, myosin, MYH14
    Summary: myosin heavy chain 14

Clinical features

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