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Cardiovascular Diseases > Vascular Diseases > Vasculitis > Behcet Syndrome
Stomatognathic Diseases > Mouth Diseases > Behcet Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Hereditary Autoinflammatory Diseases > Behcet Syndrome
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Hereditary Autoinflammatory Diseases > Behcet Syndrome
... > Eye Diseases > Uveal Diseases > Uveitis > Panuveitis > Uveitis, Anterior > Behcet Syndrome
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Vascular > Behcet Syndrome

Término preferido

Behcet Syndrome  

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Tipo

  • mesh:Descriptor

Definición

  • 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.

Concepto genérico

Etiquetas alternativas

  • Adamantiades-Behcet Disease
  • Behcet Disease
  • Behçet Disease
  • Behcet Triple Symptom Complex
  • Behcet's Disease
  • Behcet's Syndrome
  • Old Silk Route Disease
  • Triple Symptom Complex
  • Triple-Symptom Complex

En otras lenguas

  • Maladie de Behçet

    francés

  • Grande aphtose de Touraine
  • Syndrome d'Adamantiades-Behçet
  • Syndrome de Behçet
  • Syndrome oculo-muco-cutané de Behçet
  • Trisyndrome de Behçet

URI

http://data.loterre.fr/ark:/67375/JVR-K9GTTP19-W

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