SE-ATLAS

Enthesitis-related juvenile idiopathic arthritis Familial Mediterranean fever Hyperimmunoglobulinemia D with periodic fever Hyper-IgE syndrome Common variable immunodeficiency Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis Unexplained periodic fever syndrome Netherton syndrome PFAPA syndrome Tumor necrosis factor receptor 1 associated periodic syndrome Recurrent infections associated with rare immunoglobulin isotypes deficiency Pyoderma gangrenosum Chronic mucocutaneous candidiasis Juvenile dermatomyositis NLRP3-associated autoinflammatory disease Vasculitis Behçet disease Scleroderma Diamond-Blackfan anemia Pediatric systemic lupus erythematosus Shwachman-Diamond syndrome Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency Immune thrombocytopenia Kawasaki disease Transient hypogammaglobulinemia of infancy Reactive arthritis 22q11.2 deletion syndrome Shiga toxin-associated hemolytic uremic syndrome Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis Systemic-onset juvenile idiopathic arthritis Non-severe combined immunodeficiency X-linked agammaglobulinemia Blau syndrome Acquired neutropenia Severe congenital neutropenia Evans syndrome Psoriasis-related juvenile idiopathic arthritis