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Differential Diagnosis For Constitutional symptoms: Allergic, Collagen, Auto-Immune Disorders

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Allergic, Collagen, Auto-Immune Disorders: next: Metabolic Causes: Crohn's disease (Regional enteritis); Anaphylaxis, generalized; Nephritis, allergic interstitial, acute; Rheumatic arthritis/acute; Collagen-vascular disease; Dressler's syndrome; Juvenile rheumatoid arthritis/Stills d; Lupus nephritis; Ulcerative jejunoileitis,nongranulomat.; Collagen disease; Ulcerative colitis arthritis; Allergic granulomatosis, lung; Aortitis, giant cell; Arteritis, giant cell/non-cranial; Churg-Strauss syndrome; Encephalitis, hemorrhagic, acute; Encephalomyelitis, necrotizing hem. ac.; Eosinophilic peritonitis; Goodpasture's syndrome; Hypersensitivity pneumonitis/alveolitis; Purpura fulminans; Reyes syndrome; Rheumatic carditis, active; Stevens-Johnson syndrome; Temporal/Craniotemporal arteritis; Transfusion/anaphylaxis foreign protein; Crohn's colitis/large bowel; Dermatitis, exfoliative, generalized; Lupus cerebritis; Myocarditis, giant cell type; Pneumonia, desquamative, interstitial; Pneumonitis, collagen vascular disease; Rheumatic fever; Rheumatoid arthritis; Serum sickness; Sprue (gluten enteropathy); Takayasu's pulseless aortitis synd.; Ulcerative colitis; Adult Stills disease/RA presentation; Arthritis of inflammatory bowel disease; Autoimmune hepatitis (Plasma cell); Carrington's pulmonary eosinophilia; Collagenosis, unclassified; Dermatomyositis; Dermatomyositis/childhood type; Drug induced Lupus (SLE)-; Enterocolitis arthritis; Erythema multiforme; Erythema nodosum; Juvenile chronic arthritis (rheumatoid); Loeffler's Eosinophilic Pneumonitis, acute/PIE; Lupus erythematosis, systemic; Mixed connective tissue disease (MCTD)/Undifferentiated; Necrotizing angiitis, cutaneous; Necrotizing vasculitis process; Pigeon breeder's lung/disease; Polyarteritis nodosa; Polymyalgia rheumatica; Polymyositis; Reiters Syndrome; Rheumatoid arteritis/vasculitis; Rheumatoid lung disease; Thyroiditis, granulomatous, subacute; Ulcerative proctitis; Polyarteritis nodosa, infantile; Polychondritis, relapsing; Hashimotos Encephalitis

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