Visão selecionada em Inglês
| Descritor em português: | Síndrome de Behçet | ||||||
| Descritor em inglês: | Behcet Syndrome | ||||||
| Descritor em espanhol: |
Síndrome de Behçet
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| Descritor em francês: | Maladie de Behçet | ||||||
| Termo(s) alternativo(s): |
Adamantiades Behcet Disease Adamantiades-Behcet Disease Adamantiades-Behcet Diseases Behcet Disease Behcet Triple Symptom Complex Behcet's Disease Behcet's Syndrome Behcets Syndrome Behçet Disease Behçet Diseases Complex, Triple Symptom Complices, Triple Symptom Disease, Adamantiades-Behcet Disease, Behçet Diseases, Adamantiades-Behcet Diseases, Behçet Old Silk Route Disease Symptom Complex, Triple Symptom Complices, Triple Triple Symptom Complex Triple Symptom Complices Triple-Symptom Complex |
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| Código(s) hierárquico(s): |
C07.465.075 C11.941.879.780.880.200 C14.907.940.100 C16.320.382.250 C17.800.827.368.250 C17.800.862.150 |
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| Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D001528 | ||||||
| Nota de escopo: | Rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and uveitis with hypopyon. The neuro-ocular form may cause blindness and death. SYNOVITIS; THROMBOPHLEBITIS; gastrointestinal ulcerations; RETINAL VASCULITIS; and OPTIC ATROPHY may occur as well. |
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| Nota de indexação: | in translations spell Behçet's, not Behcet's |
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| Qualificadores permitidos: |
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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| Nota MeSH pública: | 2003; see BEHCET'S SYNDROME 1963-2002 |
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| Nota histórica: | 2003 (1963) |
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| Identificador DeCS: | 28255 | ||||||
| ID do descritor: | D001528 | ||||||
| Classificação da NLM: | WW 240 | ||||||
| Documentos indexados na Biblioteca Virtual em Saúde (BVS): | Clique aqui para acessar os documentos da BVS | ||||||
| Data de estabelecimento: | 01/01/2003 | ||||||
| Data de entrada: | 01/01/1999 | ||||||
| Data de revisão: | 16/01/2020 |
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DISEASES
Eye Diseases [C11]Eye Diseases
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Behcet Syndrome
- Conceito preferido
| Identificador do conceito |
M0002296 |
| Nota de escopo | Rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and uveitis with hypopyon. The neuro-ocular form may cause blindness and death. SYNOVITIS; THROMBOPHLEBITIS; gastrointestinal ulcerations; RETINAL VASCULITIS; and OPTIC ATROPHY may occur as well. |
| Termo preferido | Behcet Syndrome |
| Termo(s) alternativo(s) |
Adamantiades Behcet Disease Adamantiades-Behcet Disease Adamantiades-Behcet Diseases Behcet Disease Behcet Triple Symptom Complex Behcet's Disease Behcet's Syndrome Behcets Syndrome Behçet Disease Behçet Diseases Complex, Triple Symptom Complices, Triple Symptom Disease, Adamantiades-Behcet Disease, Behçet Diseases, Adamantiades-Behcet Diseases, Behçet Old Silk Route Disease Symptom Complex, Triple Symptom Complices, Triple Triple Symptom Complex Triple Symptom Complices Triple-Symptom Complex |
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