Variants
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Autosomal recessive nonsyndromic hearing loss 97

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Description

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

MONDO

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

18

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Genes

External Links

  • OMIM

    616705

  • Orphanet
  • HPO
  • Medgen

    C4084709

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