Disease
Division of Rheumatology
- rheumatic fever
- Raynaud's disease
- Felty syndrome
- febrile neutrophilic skin disease
- rheumatic chorea
- Type I immunoblastic lymphadenopathy
- mucocutaneous lymph node syndrome
- Still's disease
- Raynaud's syndrome
- Dermatomyositis
- Behcet's syndrome
- Behcet's disease
- Behcet's disease
- late-onset hypogammaglobulinemia
- polyarteritis
- polymyositis
- Kashin-Beck disease
- amyloidosis
- Calcium pyrophosphate dihydrate crystal deposition disease
- polymyalgia rheumatica
- mastocytosis
- allergic asthma
- Hyperuricemia
- Sjögren's syndrome
- lupus erythematosus
- mixed connective tissue disease
- alkaline calcium phosphate crystal deposition disease
- giant cell arteritis
- polyarteritis nodosa
- nodular panniculitis
- sarcoidosis
- acute lymphangitis
- Rheumatoid Arthritis
- Chronic mucocutaneous candidiasis
- chronic granulomatous disease
- discoid lupus erythematosus
- ankylosing spondylitis
- Hydroxyapatite deposition disease
- Reiter syndrome
- eosinophilic fasciitis
- Type IV hypersensitivity disease
- Type III hypersensitivity disease
- food allergies and intolerances
- gout
- gouty arthritis
- physical allergy
- serum sickness
- selective IgA deficiency
- primary immunodeficiency disease
- psoriatic arthritis
- hereditary complement deficiency
- hereditary angioedema
- Drug allergy
- severe combined immunodeficiency disease
- Type I hypersensitivity disease
- scleroderma
- overlap syndrome
- systemic lupus erythematosus
- rheumatoid arthritis
- fibromyalgia
- systemic lupus erythematosus arthritis
- Relapsing polychondritis scleritis
- recurrent rheumatism
- Microvirus B19 Infectious Rheumatism
- congenital pangammaglobulinemia
- fibromyalgia syndrome
- Mental disorders associated with Behcet's disease
- Ehler-Danlos syndrome
- fibrotic syndrome
- systemic lupus erythematosus
- fibromyalgia syndrome
- scleredema
- rheumatoid arthritis scleritis in adults
- lupus nephritis
- Austin type infantile sulfatosis
- Microscopic polyangiitis
- Mental disorders associated with polymyositis and dermatomyositis
- Giant cell arteritis and polymyalgia rheumatica
- allergic cutaneous nodular vasculitis
- Relapsing fever nodular nonsuppurative panniculitis
- rheumatic marginal erythema
- acute septic arthritis
- lupus-like syndrome
- Adult Still's disease
- chronic mucocutaneous candidiasis
- prevasculitic syndrome
- Kidney damage in rheumatoid arthritis
- combined immunodeficiency disease
- systemic vasculitis
- systemic lupus erythematosus scleritis
- Dermatomyositis and Polymyositis
- Behcet's disease scleritis
- disseminated eosinophilic collagen disease
- Brucella arthritis
- CM1 gangliosidosis
- polyarteritis nodosa scleritis
- cutaneous leukocytoclastic vasculitis
- Human Immunodeficiency Virus Infectious Kidney Damage
- Amyloid peripheral neuropathy
- Polymyositis - Dermatomyositis
- multicentric reticulohistiocytosis
- Type II immunoblastic lymphadenopathy
- Ferty syndrome
- Recurrent cutaneous necrotizing eosinophilic vasculitis
- Mannosidosis
- Hepatitis virus-related rheumatism
- Allergic granulomatous vasculitis-associated scleritis
- Allergic vasculitis and granulomatous disease
- cold panniculitis
- mixed connective tissue disease
- acute lipodermatosclerosis
- Familial Mediterranean Fever
- segmental hyaline vasculitis
- antiphospholipid antibody syndrome
- Antibody immunodeficiency disease
- Cochrane syndrome
- Wright syndrome
- Osteoarthritis in the elderly
- rheumatoid arthritis in the elderly
- pseudoxanthoma elastica
- Wright syndrome scleritis
- mucopolysaccharidosis
- mucopolysaccharidosis type 1
- mucopolysaccharidosis type Ⅱ
- mucopolysaccharidosis type Ⅲ
- mucopolysaccharidosis type Ⅳ
- mucopolysaccharidosis type V
- mucopolysaccharidosis type VI
- mucopolysaccharidosis type VII
- mucopolysaccharidosis type VIII
- mucolipidosis type 1
- mucolipidosis type II
- mucolipidosis type Ⅲ
- mucolipidosis type Ⅳ
- Poncet syndrome
- ankylosing spondylitis scleritis
- Pigmented purpuric lichenoid dermatosis
- Eosinophilia-myalgia syndrome
- Fucosidosis
- idiopathic arthralgia syndrome
- Aspartyl glucosamineuria
- Phagocytosis deficiency
- livedo reticularis and livedoid vasculitis
- Wegener's granulomatosis
- Wegener's granulomatosis
- undifferentiated connective tissue disease
- Mental disorders associated with systemic lupus erythematosus
- Uveitis associated with systemic lupus erythematosus
- Myelopathy due to systemic lupus erythematosus
- thrombophlebitis
- nodular liquefying panniculitis
- subacute cutaneous lupus erythematosus
- drug-induced lupus
- hereditary hyperuricemia
- Mental disorders associated with scleroderma
- migratory nodular panniculitis
- stasis subcutaneous sclerosis
- histiocytic phagocytic panniculitis
- relapsing polychondritis
- polymyositis
- Rheumatism
- tophi
- postpartum rheumatism
- rheumatic diseases
- hip osteoarthritis
- amyopathic dermatomyositis
- Spondyloarthritis
- internal wetness
- rheumatic bone disease