| Descriptor English: | Behcet Syndrome | ||||||
| Descriptor Spanish: |
Síndrome de Behçet
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| Descriptor Portuguese: | Síndrome de Behçet | ||||||
| Descriptor French: | Maladie de Behçet | ||||||
| Entry term(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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| Tree number(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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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D001528 | ||||||
| Scope note: | 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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| Annotation: | in translations spell Behçet's, not Behcet's |
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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: | 2003; see BEHCET'S SYNDROME 1963-2002 |
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| History Note: | 2003 (1963) |
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| DeCS ID: | 28255 | ||||||
| Unique ID: | D001528 | ||||||
| NLM Classification: | WW 240 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2003/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2020/01/16 |
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DISEASES
Eye Diseases [C11]Eye Diseases
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Behcet Syndrome
- Preferred
| Concept UI |
M0002296 |
| Scope note | 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. |
| Preferred term | Behcet Syndrome |
| Entry term(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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