SE-ATLAS

Drug-induced lupus erythematosus AL amyloidosis AA amyloidosis AGel amyloidosis Wild type ATTR amyloidosis Hughes-Stovin syndrome ATTRV30M amyloidosis Hereditary amyloidosis with primary renal involvement Tenosynovial giant cell tumor Amyloidosis Familial Mediterranean fever Hyperimmunoglobulinemia D with periodic fever Cutaneous small vessel vasculitis Sterile multifocal osteomyelitis with periostitis and pustulosis ATTRV122I amyloidosis Gorham-Stout disease Infantile onset panniculitis with uveitis and systemic granulomatosis Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis Overlap myositis Generalized pustular psoriasis Idiopathic recurrent pericarditis Immunoglobulin A vasculitis Unexplained periodic fever syndrome Granulomatosis with polyangiitis Overlapping connective tissue disease Pyomyositis MAGIC syndrome Dermatomyositis PFAPA syndrome CINCA syndrome Erdheim-Chester disease Tumor necrosis factor receptor 1 associated periodic syndrome Unclassified vasculitis Juvenile idiopathic arthritis Wild type ABeta2M amyloidosis Polyarteritis nodosa Pyoderma gangrenosum Drug-induced vasculitis Reye syndrome Idiopathic juvenile osteoporosis Unexplained long-lasting fever/inflammatory syndrome Reynolds syndrome Proteasome-associated autoinflammatory syndrome Rheumatic fever Primary angiitis of the central nervous system Majeed syndrome Autoinflammatory syndrome Schnitzler syndrome Cogan syndrome NLRP3-associated autoinflammatory disease Sweet syndrome IgG4-related dacryoadenitis and sialadenitis Juvenile dermatomyositis Predominantly medium-vessel vasculitis PAPA syndrome JMP syndrome Predominantly large-vessel vasculitis SAPHO syndrome Idiopathic achalasia Periodic fever syndrome Vasculitis Buerger disease Sarcoidosis Predominantly small-vessel vasculitis Behçet disease 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