Variants
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Autosomal recessive nonsyndromic hearing loss 23

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Description

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the PCDH15 gene.

MONDO

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

36

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Genes

External Links

  • OMIM

    609533

  • Orphanet
  • HPO
  • Medgen

    C1836027

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