arthrocutaneouveal granulomatosis (ACUG); granulomatous synovitis with uveitis & cranial neuropathies; familial juvenile systemic granulomatosis; Jabs syndrome; Blau syndrome; familial granulomatous inflammatory arthritis, dermatitis & uveitis

Epidemiology

rare

Genetics

• autosomal dominant
• associated with defects in NOD2 are the cause of

Clinical manifestations

• early-onset granulomatous arthritis, uveitis & skin rash

More general terms

• granulomatosis
• syndrome

Database

• OMIM: https://mirror.omim.org/entry/186580