Variants
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Autosomal recessive nonsyndromic hearing loss 8

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Description

An autosomal recessive nonsyndromic deafness that has material basis in mutation in the TMPRSS3 gene on chromosome 21q22.

MONDO

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

107

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Genes

External Links

  • OMIM

    601072

  • Orphanet
  • HPO
  • Medgen

    C1832827

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