Blau syndrome

Also known as ARTHROCUTANEOUVEAL GRANULOMATOSIS, Jabs syndrome, Granulomatous arthritis of childhood, Synovitis granulomatous with uveitis and cranial neuropathies, Granulomatous Inflammatory Arthritis, Dermatitis, and Uveitis, Familial, ACUG, Pediatric Granulomatous Arthritis, Granulomatosis, Familial, Blau Type

autosomal dominant disease characterized by familial granulomatous arthritis, uveitis and skin granulomas. It has material basis in mutations in the NOD2/CARD15 genes