| Descriptor English: | Uveomeningoencephalitic Syndrome | ||||||
| Descriptor Spanish: |
Síndrome Uveomeningoencefálico
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| Descriptor Portuguese: | Síndrome Uveomeningoencefálica | ||||||
| Descriptor French: | Syndrome uvéo-méningo-encéphalique | ||||||
| Entry term(s): |
Disease, Vogt-Koyanagi-Harada Syndrome, Uveomeningoencephalitic Syndrome, VKH Syndrome, VKH (Vogt Koyanagi Harada) Syndrome, Vogt Koyanagi Harada Syndrome, Vogt-Koyanagi-Harada Uveomeningoencephalitides Uveomeningoencephalitis VKH (Vogt Koyanagi Harada) Syndrome VKH Syndrome VKH Syndrome (Vogt Koyanagi Harada) Vogt Koyanagi Harada Disease Vogt Koyanagi Harada Syndrome Vogt-Koyanagi-Harada Disease Vogt-Koyanagi-Harada Syndrome |
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| Tree number(s): |
C10.114.843 C11.941.879.980 C20.111.258.925 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D014607 | ||||||
| Scope note: | A syndrome characterized by bilateral granulomatous UVEITIS with IRITIS and secondary GLAUCOMA, premature ALOPECIA, symmetrical VITILIGO, poliosis circumscripta (a strand of depigmented hair), HEARING DISORDERS, and meningeal signs (neck stiffness and headache). Examination of the cerebrospinal fluid reveals a pattern consistent with MENINGITIS, ASEPTIC. (Adams et al., Principles of Neurology, 6th ed, p748; Surv Ophthalmol 1995 Jan;39(4):265-292) |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital 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 |
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| Public MeSH Note: | 1991; was see under UVEITIS 1965-1990 |
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| History Note: | 1991(1965); was see under UVEITIS 1965-1990 |
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| Entry Version: | UVEOMENINGOENCEPH SYNDROME |
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| DeCS ID: | 27884 | ||||||
| Unique ID: | D014607 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2015/06/05 |
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DISEASES
Eye Diseases [C11]Eye Diseases
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Uveomeningoencephalitic Syndrome
- Preferred
| Concept UI |
M0022447 |
| Scope note | A syndrome characterized by bilateral granulomatous UVEITIS with IRITIS and secondary GLAUCOMA, premature ALOPECIA, symmetrical VITILIGO, poliosis circumscripta (a strand of depigmented hair), HEARING DISORDERS, and meningeal signs (neck stiffness and headache). Examination of the cerebrospinal fluid reveals a pattern consistent with MENINGITIS, ASEPTIC. (Adams et al., Principles of Neurology, 6th ed, p748; Surv Ophthalmol 1995 Jan;39(4):265-292) |
| Preferred term | Uveomeningoencephalitic Syndrome |
| Entry term(s) |
Disease, Vogt-Koyanagi-Harada Syndrome, Uveomeningoencephalitic Syndrome, VKH Syndrome, VKH (Vogt Koyanagi Harada) Syndrome, Vogt Koyanagi Harada Syndrome, Vogt-Koyanagi-Harada Uveomeningoencephalitides Uveomeningoencephalitis VKH (Vogt Koyanagi Harada) Syndrome VKH Syndrome VKH Syndrome (Vogt Koyanagi Harada) Vogt Koyanagi Harada Disease Vogt Koyanagi Harada Syndrome Vogt-Koyanagi-Harada Disease Vogt-Koyanagi-Harada Syndrome |
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