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Concept information

Preferred term

Usher Syndromes  

Type

  • Topical Descriptor

Entry terms

  • Deafness Retinitis Pigmentosa Syndrome
  • Deafness-Retinitis Pigmentosa Syndrome
  • Deafness-Retinitis Pigmentosa Syndromes
  • Dystrophia Retinae Pigmentosa Dysostosis Syndrome
  • Dystrophia Retinae Pigmentosa-Dysostosis Syndrome
  • Graefe Usher Syndrome
  • Graefe-Usher Syndrome
  • Hallgren Syndrome
  • Pigmentosa Syndromes, Deafness-Retinitis
  • Retinitis Pigmentosa Deafness Syndrome
  • Retinitis Pigmentosa-Deafness Syndrome
  • Retinitis Pigmentosa-Deafness Syndromes
  • Syndrome, Deafness-Retinitis Pigmentosa
  • Syndrome, Graefe-Usher
  • Syndrome, Hallgren
  • Syndrome, Retinitis Pigmentosa-Deafness
  • Syndromes, Deafness-Retinitis Pigmentosa
  • Syndromes, Retinitis Pigmentosa-Deafness
  • Syndrome, Usher's
  • Usher's Syndrome
  • Ushers Syndrome
  • Usher Syndrome

Scope note

  • Autosomal recessive hereditary disorders characterized by congenital SENSORINEURAL HEARING LOSS and RETINITIS PIGMENTOSA. Genetically and symptomatically heterogeneous, clinical classes include type I, type II, and type III. Their severity, age of onset of retinitis pigmentosa and the degree of vestibular dysfunction are variable.

History note

  • 2006

In other languages

URI

http://www.yso.fi/onto/mesh/D052245

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