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X-linked Agammaglobulinemia | |
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CD40 Ligand Deficiency | |
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Activation-induced Cytidine Deaminase Deficiency | |
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Common Variable Immunodeficiency | |
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X-linked Severe Combined Immunodeficiency | |
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Adenosine Deaminase Deficiency | |
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Omenn Syndrome | |
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MHC Class II Deficiency | |
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DiGeorge Syndrome | |
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Acquired Immune Deficiency Syndrome (AIDS) | |
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Graft-Versus-Host Disease | |
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MHC Class I Deficiency | |
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X-linked Lymphoproliferative Syndrome | |
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Hemophagocytic Lymphohistiocytosis | |
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Chediak-Higashi Syndrome | |
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Wiskott-Aldrich Syndrome | |
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Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy | |
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Immune Dysregulation, Polyendocrinopathy, Enteropathy X-linked Disease | |
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Autoimmune Lymphoproliferative Syndrome (ALPS) | |
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Hyper IgE Syndrome | |
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Ataxia Telangiectasia | |
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Warts, Hypogammaglobulinemia, Infections, and Myelokathexis (WHIM) Syndrome | |
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X-linked Hypohidrotic Ectodermal Dysplasia and Immunodeficiency | |
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Interferon- Receptor Deficiency | |
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Severe Congenital Neutropenia | |
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Chronic Granulomatous Disease | |
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Leukocyte Adhesion Deficiency | |
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Recurrent Herpes Simplex Encephalitis | |
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Interleukin 1 Receptor-associated Kinase 4 Deficiency | |
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Congenital Asplenia | |
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Hereditary Angioedema | |
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Factor I Deficiency | |
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Deficiency of the C8 Complement Component | |
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Hereditary Periodic Fever Syndromes | |
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Systemic Onset Juvenile Idiopathic Arthritis | |
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Rheumatoid Arthritis | |
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Systemic Lupus Erythematosus | |
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Mixed Essential Cryoglobulinemia | |
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Crohn's Disease | |
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Multiple Sclerosis | |
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Autoimmune Hemolytic Anemia | |
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Myasthenia Gravis | |
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Pemphigus Vulgaris | |
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Celiac Disease | |
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Acute Infectious Mononucleosis | |
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Hemolytic Disease of the Newborn | |
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Toxic Shock Syndrome | |
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Lepromatous Leprosy | |
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Acute Systemic Anaphylaxis | |
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Allergic Asthma | |
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Atopic Dermatitis | |
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Drug-induced Serum Sickness | |
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Contact Sensitivity to Poison Ivy | |
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Answers | |
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Figure Acknowledgments | |
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Index | |