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