| Descriptor English: | Usher Syndromes | ||||
| Descriptor Spanish: |
Síndromes de Usher
| ||||
| Descriptor Portuguese: | Síndromes de Usher | ||||
| Descriptor French: | Syndromes d'Usher | ||||
| Entry term(s): |
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 And Congenital Deafness 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 Syndrome, Usher Syndrome, Usher's Syndromes, Deafness-Retinitis Pigmentosa Syndromes, Retinitis Pigmentosa-Deafness Syndromes, Usher 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 Ushers Syndrome |
||||
| 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 |
||||
| RDF Unique Identifier: | https://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. |
||||
| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
||||
| Previous Indexing: |
Deafness (1972-2005) Hearing Loss, Sensorineural (1983-2005) Retinitis Pigmentosa (1972-2005) Syndrome (1972-2005) |
||||
| Public MeSH Note: | 2006 |
||||
| History Note: | 2006 |
||||
| DeCS ID: | 50480 | ||||
| Unique ID: | D052245 | ||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
| Date Established: | 2006/01/01 | ||||
| Date of Entry: | 2005/06/30 | ||||
| Revision Date: | 2013/07/08 |
-
DISEASES
Eye Diseases [C11]Eye Diseases -
DISEASES
Eye Diseases [C11]Eye Diseases
|
|
Usher Syndromes
- Preferred
Usher Syndrome, Type III
- Narrower
Usher Syndrome, Type I
- Narrower
Usher Syndrome, Type II
- Narrower
| Concept UI |
M0483844 |
| 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. |
| Preferred term | Usher Syndromes |
| Entry term(s) |
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 Syndrome, Usher Syndrome, Usher's Syndromes, Deafness-Retinitis Pigmentosa Syndromes, Retinitis Pigmentosa-Deafness Syndromes, Usher Usher Syndrome Usher's Syndrome Ushers Syndrome |
| Concept UI |
M0483846 |
| Preferred term | Usher Syndrome, Type III |
| Entry term(s) |
Usher Syndrome, Type 3 |
| Concept UI |
M0483845 |
| Preferred term | Usher Syndrome, Type I |
| Entry term(s) |
Retinitis Pigmentosa And Congenital Deafness Usher Syndrome, Type 1 Usher Syndrome, Type 1A Usher Syndrome, Type I, French Variety |
| Concept UI |
M0483847 |
| Preferred term | Usher Syndrome, Type II |
| Entry term(s) |
Usher Syndrome, Type IId |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
