Concept information
Preferred term
Usher Syndromes
Type
-
Topical Descriptor
Broader concept
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
-
Finnish
-
DRD
-
dystrophia retinae pigmentosa - dysacusis
-
Usher
-
Usher-oireyhtymä
-
Usher-oireyhtymät
-
Usher-syndrooma
-
Swedish
URI
http://www.yso.fi/onto/mesh/D052245
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