It is defined as a disorder in which there is a granulamatous arthritis, iritis as well as the skin granuloma. It is familial and autosomal dominant in nature. It has features which resemble both the sarcoidosis as well as granuloma annulare. It is rare and autosomal dominant in nature. It is in link with the NOD2. It is rare and has unknown etiology.
It includes the arthritis, iritis as well as the skin granuloma.
It includes the genetic causes mainly.
It includes the use of visual examination only.