Asklepios Klinik Altona Assigned 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