SE-ATLAS

Lupus erythematodes, Medikamenteninduzierter AL-Amyloidose AA-Amyloidose Agel-Amyloidose Wildtyp-ATTR-Amyloidose Hughes-Stovin-Syndrom ATTRV30M-Amyloidose Hereditäre Amyloidose mit vorwiegender Nierenbeteiligung Tenosynovialer Riesenzelltumor Amyloidose Mittelmeerfieber, familiäres Hyperimmunglobulinämie D mit Rückfallfieber Kutane Vaskulitis kleiner Gefäße Sterile multifokale Osteomyelitis mit Periostitis und Pustulose ATTRV122I-Amyloidose Gorham-Stout-Krankheit Pannikulitis mit Uveitis und systemischer Granulomatose, infantile Form Chronische nicht-bakterielle Osteomyelitis/rezidivierende multifokale Osteomyelitis Myositis-Overlap-Syndrom Generalisierte pustulöse Psoriasis Perikarditis, idiopathische rekurrente Immunoglobulin A-Vaskulitis Periodisches Fiebersyndrom ohne identifizierte Ursache Granulomatose mit Polyangiitis Mischkollagenose, überlappende Pyomyositis MAGIC-Syndrom Dermatomyositis PFAPA-Syndrom CINCA-Syndrom Erdheim-Chester-Krankheit Tumornekrosefaktor-Rezeptor 1-assoziiertes periodisches Fieber-Syndrom Vaskulitis, unklassifizierte Arthritis, idiopathische juvenile ABeta2M-Amyloidose, Wild-Typ Polyarteriitis nodosa Pyoderma gangraenosum Vaskulitis, Medikamenten-induzierte Reye-Syndrom Osteoporose, idiopathische juvenile Fieber-Syndrom, langanhaltendes unerklärbares Reynolds-Syndrom Proteasom-assoziiertes autoinflammatorisches Syndrom Rheumatisches Fieber Primäre Angiitis des Zentralnervensystems Majeed-Syndrom Autoinflammatorisches Syndrom Schnitzler-Syndrom Cogan-Syndrom Cryopyrin-assoziiertes periodisches Syndrom Sweet-Syndrom IgG4-assoziierte Dakryoadenitis und Sialoadenitis Dermatomyositis, juvenile Vaskulitis mittelgroßer Gefäße PAPA-Syndrom JMP-Syndrom Vaskulitis großer Gefäße SAPHO-Syndrom Achalasie, idiopathische Periodisches Fiebersyndrom Vaskulitis Buerger-Krankheit Sarkoidose Vaskulitis kleiner Gefäße Behçet-Syndrom Erythema elevatum diutinum Diffuse cutaneous systemic sclerosis Anti-neutrophil cytoplasmic antibody-associated vasculitis Immune complex mediated vasculitis Undifferentiated connective tissue syndrome CANDLE syndrome Autoimmune pancreatitis Giant cell arteritis Familial cold urticaria Mixed cryoglobulinemia type III Mixed cryoglobulinemia type II Myalgia-eosinophilia syndrome associated with tryptophan Mixed connective tissue disease Variant ABeta2M amyloidosis Interstitial granulomatous dermatitis with arthritis Hypocomplementemic urticarial vasculitis ALys amyloidosis Limited cutaneous systemic sclerosis AApoAI amyloidosis AApoAII amyloidosis CREST syndrome AFib amyloidosis Limited systemic sclerosis Systemic sclerosis Sneddon syndrome Juvenile polymyositis Polymyalgia rheumatica Progeria-associated arthropathy Systemic autoimmune disease Osteochondritis of tarsal/metatarsal bone Autosomal systemic lupus erythematosus Adult-onset Still disease Felty syndrome Rare rheumatologic disease Classical Ehlers-Danlos syndrome Takayasu arteritis Postinfectious vasculitis Ehlers-Danlos syndrome type 1 Retinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Reactive arthritis Autoimmune pancreatitis type 1 Nakajo-Nishimura syndrome Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Ehlers-Danlos syndrome type 2 Autoimmune pancreatitis type 2 Cryoglobulinemic vasculitis Rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies Oligoarticular juvenile idiopathic arthritis IgG4-related disease Muckle-Wells syndrome Unspecified juvenile idiopathic arthritis Intermittent hydrarthrosis Hereditary periodic fever syndrome Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies Hereditary ATTR amyloidosis Hypoplasminogenemia Granulomatous autoinflammatory syndrome Primary systemic amyloidosis Microscopic polyangiitis Relapsing polychondritis Eosinophilic granulomatosis with polyangiitis Pyogenic autoinflammatory syndrome Polyarticular juvenile idiopathic arthritis NLRP12-associated hereditary periodic fever syndrome Calciphylaxis cutis Blau syndrome Polymyositis Primary localized amyloidosis Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation Familial calcium pyrophosphate deposition Systemic capillary leak syndrome PASH syndrome Visceral calciphylaxis Mixed autoinflammatory and autoimmune syndrome Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Calciphylaxis Enthesitis-related juvenile idiopathic arthritis Psoriasis-related juvenile idiopathic arthritis Unclassified autoinflammatory syndrome Kawasaki disease