Variants
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Autosomal dominant nonsyndromic hearing loss 2B

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Description

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the GJB3 gene.

MONDO

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

5

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Genes

External Links

  • OMIM

    612644

  • Orphanet
  • HPO
  • Medgen

    C2675236

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