Congenital Asplenia | |
Chronic Granulomatous Disease | |
Leukocyte Adhesion Deficiency | |
Hereditary Angioneurotic Edema | |
Factor I Deficiency | |
Deficiency of the C8 Complement Component | |
Hereditary Periodic Fever Syndromes | |
Interleukin Receptor-associated Kinase Deficiency | |
X-linked Hypohydrotic Ectodermal Dysplasia and Immunodeficiency | |
X-linked Agammaglobulinemia | |
X-linked Hyper IgM Syndrome | |
Activation-induced Cytidine Deaminase (AID) Deficiency | |
Common Variable Immunodeficiency | |
X-linked Severe Combined Immunodeficiency | |
Adenosine Deaminase Deficiency | |
Omenn Syndrome | |
MHC Class I Deficiency | |
MHC Class II Deficiency | |
Multiple Myeloma | |
T-Cell Lymphoma | |
Interferon-? Receptor Deficiency | |
Wiskott-Aldrich Syndrome | |
X-linked Lymphoproliferative Syndrome | |
Autoimmune Lymphoproliferative Syndrome (ALPS) | |
Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked Disease | |
Toxic Shock Syndrome | |
Acute Infectious Mononucleosis | |
Mixed Essential Cryoglobulinemia | |
Rheumatic Fever | |
Lepromatous Leprosy | |
Acquired Immune Deficiency Syndrome (AIDS) | |
Acute Systemic Anaphylaxis | |
Allergic Asthma | |
Atopic Dermatitis | |
Drug-Induced Serum Sickness | |
Celiac Disease | |
Contact Sensitivity to Poison Ivy | |
Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy (APECED) | |
Autoimmune Hemolytic Anemia | |
Myasthenia Gravis | |
Rheumatoid Arthritis | |
Systemic Lupus Erythematosus | |
Multiple Sclerosis | |
Hemolytic Disease of the Newborn | |
A Kidney Graft for Complications of Autoimmune Insulin-Dependent Diabetes Mellitus | |
Graft-Versus-Host Disease | |
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