Variants
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Autosomal dominant nonsyndromic hearing loss 17

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Description

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYH9 gene.

MONDO

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

203

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Genes

External Links

  • OMIM

    603622

  • Orphanet
  • HPO
  • Medgen

    C1863659

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