SE-ATLAS

Cryoglobulinemic vasculitis Genetic inflammatory or rheumatoid-like osteoarthropathy IgG4-related retroperitoneal fibrosis PFAPA syndrome SAPHO syndrome Common variable immunodeficiency Sydenham chorea Immune thrombocytopenia Adult-onset Still disease Primary angiitis of the central nervous system NLRP12-associated hereditary periodic fever syndrome Periodic fever-infantile enterocolitis-autoinflammatory syndrome Tumor necrosis factor receptor 1 associated periodic syndrome Vasculitis due to ADA2 deficiency Pulmonary arterial hypertension associated with connective tissue disease Hyperimmunoglobulinemia D with periodic fever Infantile-onset periodic fever-panniculitis-dermatosis syndrome Polymyositis Dermatomyositis Eosinophilic fasciitis Erdheim-Chester disease Primary Sjögren syndrome Periodic fever syndrome IgG4-related disease Overlap myositis Felty syndrome Kawasaki disease Sarcoidosis Mixed connective tissue disease Hereditary periodic fever syndrome Alkaptonuria Autosomal systemic lupus erythematosus Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis Behçet disease Granulomatosis with polyangiitis Systemic sclerosis Takayasu arteritis Immunoglobulin A vasculitis Polyarteritis nodosa NLRP3-associated autoinflammatory disease Systemic lupus erythematosus Scleroderma Familial Mediterranean fever Primary immunodeficiency Castleman-Krankheit Multizentrische Osteolyse-Nodulose-Arthropathie-Spektrum Mastozytose Mevalonazidurie Muckle-Wells-Syndrom Makrophagen-Aktivierungssyndrom CINCA-Syndrom Kälte-Urtikaria, familiäre Polyangiitis, mikroskopische