Usher Syndromes
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.
Year introduced: 2006
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Tree Number(s): C09.218.458.341.186.500.500, C09.218.458.341.887.886, C10.597.751.418.341.186.500.500, C10.597.751.418.341.887.886, C10.597.751.941.162.625.500, C11.768.585.658.500.813, C11.966.075.375.500, C16.131.077.299.500, C16.320.290.684.500, C23.888.592.763.393.341.887.886
MeSH Unique ID: D052245
Entry Terms:
- Syndromes, Usher
- Syndrome, Usher
- Usher Syndrome
- Deafness-Retinitis Pigmentosa Syndrome
- Deafness Retinitis Pigmentosa Syndrome
- Deafness-Retinitis Pigmentosa Syndromes
- Pigmentosa Syndromes, Deafness-Retinitis
- Syndrome, Deafness-Retinitis Pigmentosa
- Syndromes, Deafness-Retinitis Pigmentosa
- Dystrophia Retinae Pigmentosa-Dysostosis Syndrome
- Dystrophia Retinae Pigmentosa Dysostosis Syndrome
- Retinitis Pigmentosa-Deafness Syndrome
- Retinitis Pigmentosa Deafness Syndrome
- Retinitis Pigmentosa-Deafness Syndromes
- Syndrome, Retinitis Pigmentosa-Deafness
- Syndromes, Retinitis Pigmentosa-Deafness
- Hallgren Syndrome
- Syndrome, Hallgren
- Usher's Syndrome
- Syndrome, Usher's
- Ushers Syndrome
- Graefe-Usher Syndrome
- Graefe Usher Syndrome
- Syndrome, Graefe-Usher
- Usher Syndrome, Type I
- Retinitis Pigmentosa And Congenital Deafness
- Usher Syndrome, Type 1
- Usher Syndrome, Type 1A
- Usher Syndrome, Type I, French Variety
- Usher Syndrome, Type III
- Usher Syndrome, Type 3
- Usher Syndrome, Type II
- Usher Syndrome, Type IId
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