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Usher syndrome, type 1M

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Description

Usher syndrome type 1M (USH1M) is characterized by prelingual sensorineural hearing loss, vestibular dysfunction, and retinitis pigmentosa (Ahmed et al., 2018). For a general phenotypic description and discussion of genetic heterogeneity of Usher syndrome, see USH1 (276900).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

1

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Genes

External Links

  • OMIM

    618632

  • Orphanet
  • HPO
  • Medgen

    C5231434

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