SE-ATLAS

Adult-onset Still disease Autosomal systemic lupus erythematosus Behçet disease Blau syndrome Brittle cornea syndrome Buerger disease Bullous pemphigoid CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome CINCA syndrome CREST syndrome Catastrophic antiphospholipid syndrome Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis Common variable immunodeficiency Cryoglobulinemic vasculitis Cutaneous small vessel vasculitis Cyclic neutropenia Cytophagic histiocytic panniculitis Diffuse cutaneous systemic sclerosis Discoid lupus erythematosus Eosinophilic fasciitis Eosinophilic granulomatosis with polyangiitis Familial Mediterranean fever Familial cold urticaria Familial reactive perforating collagenosis Focal myositis Granulomatosis with polyangiitis Hereditary periodic fever syndrome Hyperimmunoglobulinemia D with periodic fever Idiopathic anterior uveitis Idiopathic juvenile osteoporosis Idiopathic panuveitis Idiopathic posterior uveitis IgG4-related aortitis Immunoglobulin A vasculitis Infantile-onset periodic fever-panniculitis-dermatosis syndrome Juvenile dermatomyositis Juvenile idiopathic arthritis Juvenile overlap myositis Juvenile polymyositis Juvenile temporal arteritis Kawasaki disease Limited cutaneous systemic sclerosis Linear IgA dermatosis Localized scleroderma Lupus erythematosus panniculitis Majeed syndrome Mevalonic aciduria Microscopic polyangiitis Mixed connective tissue disease Muckle-Wells syndrome NLRP12-associated hereditary periodic fever syndrome Neonatal antiphospholipid syndrome Neonatal dermatomyositis Neonatal lupus erythematosus Neonatal scleroderma Nodular non-suppurative panniculitis Oligoarticular juvenile idiopathic arthritis Osteonecrosis PFAPA syndrome Pediatric systemic lupus erythematosus Periodic fever-infantile enterocolitis-autoinflammatory syndrome Postinfectious vasculitis Primary Sjögren syndrome Primary angiitis of the central nervous system Primary erythromelalgia Primary polyarteritis nodosa Proteasome-associated autoinflammatory syndrome Psoriasis-related juvenile idiopathic arthritis Rare cutaneous lupus erythematosus Reynolds syndrome Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis STAT3-related early-onset multisystem autoimmune disease STING-associated vasculopathy with onset in infancy Sarcoidosis Scheuermann's disease Secondary non-traumatic avascular necrosis Secondary polyarteritis nodosa Simple cryoglobulinemia Sneddon syndrome Sterile multifocal osteomyelitis with periostitis and pustulosis Systemic sclerosis Systemic-onset juvenile idiopathic arthritis Takayasu arteritis Tenosynovial giant cell tumor Tumor necrosis factor receptor 1 associated periodic syndrome Type 1 interferonopathy Type 1 interferonopathy of childhood Unclassified vasculitis Undifferentiated connective tissue syndrome Unspecified juvenile idiopathic arthritis