NLM Logo

Usher Syndromes MeSH Descriptor Data 2023


MeSH Heading
Usher Syndromes
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
Unique ID
D052245
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D052245
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.
Entry Term(s)
Deafness-Retinitis Pigmentosa Syndrome
Dystrophia Retinae Pigmentosa-Dysostosis Syndrome
Graefe-Usher Syndrome
Hallgren Syndrome
Retinitis Pigmentosa And Congenital Deafness
Retinitis Pigmentosa-Deafness Syndrome
Usher Syndrome
Usher Syndrome, Type 1
Usher Syndrome, Type 1A
Usher Syndrome, Type 3
Usher Syndrome, Type I
Usher Syndrome, Type I, French Variety
Usher Syndrome, Type II
Usher Syndrome, Type III
Usher Syndrome, Type IId
Usher's Syndrome
Previous Indexing
Deafness (1972-2005)
Hearing Loss, Sensorineural (1983-2005)
Retinitis Pigmentosa (1972-2005)
Syndrome (1972-2005)
Public MeSH Note
2006
History Note
2006
Date Established
2006/01/01
Date of Entry
2005/06/30
Revision Date
2013/07/08
Usher Syndromes Preferred
Usher Syndrome, Type III Narrower
Usher Syndrome, Type I Narrower
Usher Syndrome, Type II Narrower
page delivered in 0.177s