<nowiki>Síndrome de Blau; syndrome de Blau; Zespół Blaua; Нәселле ювениль системалы гранулематоз синдромы; Síndrome de Blau; Blau-Syndrom; Blaun oireyhtymä; Blau syndrome; متلازمة بلاو; Blauov sindrom; Blauov sindrom; avtosomno dominantna bolezen, za katero so značilni družinski granulomatozni artritis, uveitis in kožni granulomi; seltene Erbkrankheit; An autosomal dominant disease characterized by familial granulomatous arthritis, uveitis and skin granulomas. It has material basis in mutations in the NOD2/CARD15 genes.; rzadkie, genetycznie uwarunkowane schorzenie; maladie rare; 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; BLAU SYNDROME; BLAUS; Synovitis, Granulomatous, With Uveitis and Cranial Neuropathies; BLAUS; Granulomatosis, Familial Juvenile Systemic; BLAU SYNDROME; Zespół Jabsa; arthrite pédiatrique de Granulomatous; sarcoïdose juvénile; Sindrome de Blau</nowiki>
Blau syndrome
An autosomal dominant disease characterized by familial granulomatous arthritis, uveitis and skin granulomas. It has material basis in mutations in the NOD2/CARD15 genes.