Behcet Syndrome

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34416

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.

A systemic vasculitis affecting both arteries and veins which manifests primarily as recurrent oral and genital ulceration, uveitis, characteristic rash, and arthritis. It may also cause central nervous system disease, gastrointestinal inflammation or ulceration, or thrombophlebitis.

rare chronic inflammatory disease involving the small blood vessels; of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and uveitis with hypopyon; the neuroocular form may cause blindness and death; synovitis, thrombophlebitis, gastrointestinal ulcerations, retinal vasculitis, and optic atrophy may occur as well.

C34416

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118468

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259

NICHD

A rare chronic inflammatory disorder of unknown etiology. It is characterized by the development of ulcers in the mouth and genital region and uveitis. Other signs and symptoms include arthritis, deep vein thrombosis and superficial thrombophlebitis.

Behçet Disease

Behcet's Syndrome

Morbus Behçet's Syndrome

Silk Road Disease

Behçet's Syndrome

Behçet Syndrome

Behcet Disease

Behçet-Adamantiades Syndrome

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26912

Behcet Syndrome

Behcet_s_Syndrome

Behcet Syndrome

Behcet Syndrome

C34416

Behcet Syndrome

Disease or Syndrome

C0004943

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C28193