SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases


In the following you will find the diseases that are treated in this facility:
AA amyloidosis AApoAI amyloidosis AApoAII amyloidosis AFib amyloidosis AGel amyloidosis AL amyloidosis ALys amyloidosis ATTRV122I amyloidosis ATTRV30M amyloidosis Adult-onset Still disease Amyloidosis Anti-neutrophil cytoplasmic antibody-associated vasculitis Autoimmune pancreatitis Autoimmune pancreatitis type 1 Autoimmune pancreatitis type 2 Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation Autoinflammatory syndrome Autoinflammatory syndrome of childhood Autosomal systemic lupus erythematosus Behçet disease Blau syndrome Buerger disease CANDLE syndrome CINCA syndrome CREST syndrome Calciphylaxis Calciphylaxis cutis Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis Classical Ehlers-Danlos syndrome Cogan syndrome Cryoglobulinemic vasculitis Cutaneous small vessel vasculitis Dermatomyositis Diffuse cutaneous systemic sclerosis Drug-induced lupus erythematosus Drug-induced vasculitis Ehlers-Danlos syndrome type 1 Ehlers-Danlos syndrome type 2 Enthesitis-related juvenile idiopathic arthritis Eosinophilic granulomatosis with polyangiitis Erdheim-Chester disease Erythema elevatum diutinum Familial Mediterranean fever Familial calcium pyrophosphate deposition Familial cold urticaria Felty syndrome Generalized pustular psoriasis Giant cell arteritis Gorham-Stout disease Granulomatosis with polyangiitis Granulomatous autoinflammatory syndrome Hereditary ATTR amyloidosis Hereditary amyloidosis with primary renal involvement Hereditary periodic fever syndrome Hughes-Stovin syndrome Hyperimmunoglobulinemia D with periodic fever Hypocomplementemic urticarial vasculitis Hypoplasminogenemia Idiopathic achalasia Idiopathic juvenile osteoporosis Idiopathic recurrent pericarditis IgG4-related dacryoadenitis and sialadenitis IgG4-related disease Immune complex mediated vasculitis Immunoglobulin A vasculitis Infantile onset panniculitis with uveitis and systemic granulomatosis Intermittent hydrarthrosis Interstitial granulomatous dermatitis with arthritis JMP syndrome Juvenile dermatomyositis Juvenile idiopathic arthritis Juvenile polymyositis Kawasaki disease Limited cutaneous systemic sclerosis Limited systemic sclerosis MAGIC syndrome Majeed syndrome Microscopic polyangiitis Mixed autoinflammatory and autoimmune syndrome Mixed connective tissue disease Mixed cryoglobulinemia type II Mixed cryoglobulinemia type III Muckle-Wells syndrome Myalgia-eosinophilia syndrome associated with tryptophan NLRP12-associated hereditary periodic fever syndrome NLRP3-associated autoinflammatory disease Nakajo-Nishimura syndrome Oligoarticular juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Osteochondritis of tarsal/metatarsal bone Overlap myositis Overlapping connective tissue disease PAPA syndrome PASH syndrome PFAPA syndrome Pediatric systemic lupus erythematosus Periodic fever syndrome Polyarteritis nodosa Polyarticular juvenile idiopathic arthritis Polymyalgia rheumatica Polymyositis Postinfectious vasculitis Predominantly large-vessel vasculitis Predominantly medium-vessel vasculitis Predominantly small-vessel vasculitis Primary angiitis of the central nervous system Primary localized amyloidosis Primary systemic amyloidosis Progeria-associated arthropathy Proteasome-associated autoinflammatory syndrome Psoriasis-related juvenile idiopathic arthritis Pyoderma gangrenosum Pyogenic autoinflammatory syndrome Pyomyositis Rare pediatric systemic disease Rare pediatric vasculitis Rare rheumatologic disease Rare systemic or rheumatological disease of childhood Reactive arthritis Relapsing polychondritis Retinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome Reye syndrome Reynolds syndrome Rheumatic fever Rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis SAPHO syndrome Sarcoidosis Schnitzler syndrome Sneddon syndrome Sterile multifocal osteomyelitis with periostitis and pustulosis Sweet syndrome Systemic autoimmune disease Systemic capillary leak syndrome Systemic sclerosis Takayasu arteritis Tenosynovial giant cell tumor Tumor necrosis factor receptor 1 associated periodic syndrome Unclassified autoinflammatory syndrome Unclassified vasculitis Undifferentiated connective tissue syndrome Unexplained long-lasting fever/inflammatory syndrome Unexplained periodic fever syndrome Unspecified juvenile idiopathic arthritis Variant ABeta2M amyloidosis Vasculitis Visceral calciphylaxis Wild type ABeta2M amyloidosis Wild type ATTR amyloidosis