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                                                        • Antibody Deficiency
                                                          • Phagocytic Defects
                                                            • Combined T-B Cell Defects
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                                                                • Innate Immunity Defects
                                                                  • Complement Defects
                                                                    • Autoinflammatory
                                                                      • Other Disorders
                                                                        • Syndromes
                                                                        • DISEASE LIST
                                                                          • IVIG Tutorial
                                                                            • 4p Chromosome Deletion
                                                                              • 22q11.2 Deletion Syndrome
                                                                                • Acrodermatitis Enterohepatica
                                                                                  • ALPS
                                                                                    • Alternative Complement Pathway Deficienc
                                                                                      • APECED
                                                                                        • Autosomal Agammaglobulinemia
                                                                                          • Artemis Deficiency
                                                                                            • Asplenia
                                                                                              • Ataxia Telangiectasia
                                                                                                • Barth Syndrome
                                                                                                  • Blau Syndrome
                                                                                                    • Bloom Syndrome
                                                                                                      • Branched-Chain Amino Acidurias
                                                                                                        • Cartilage Hair Hypoplasia
                                                                                                          • Cryopyrin Associated Periodic Syndrome
                                                                                                            • CD4 Lymphopenia
                                                                                                              • CD25 Deficiency
                                                                                                                • Cernunnos Deficiency
                                                                                                                  • CHARGE
                                                                                                                    • Chediak Higashi Syndrome
                                                                                                                      • Chronic Granulomatous Disease
                                                                                                                        • Chronic Mucocutaneous Candidiasis
                                                                                                                          • Classical Complement Deficiency
                                                                                                                            • Cohen Syndrome
                                                                                                                              • CTLA4 Deficiency
                                                                                                                                • CVID
                                                                                                                                  • Cyclic Neutropenia
                                                                                                                                    • Cystic Fibrosis
                                                                                                                                      • DIRA
                                                                                                                                        • DNA Ligase IV Deficiency
                                                                                                                                          • DOCK 8 Deficiency (AR Hyper IgE)
                                                                                                                                            • Dyskeratosis Congenita
                                                                                                                                              • Epidermodysplasia Verruciformis
                                                                                                                                                • Familial HLH
                                                                                                                                                  • Galactosemia
                                                                                                                                                    • GATA2 Deficiency
                                                                                                                                                      • Familial Intestinal Polyatresia
                                                                                                                                                        • Familial Mediterranean Fever
                                                                                                                                                          • Hyper IgE Syndrome
                                                                                                                                                            • Fanconi Pancytopenia
                                                                                                                                                              • Glycogen Storage Disease Ia/Ib
                                                                                                                                                                • Griscelli Syndrome
                                                                                                                                                                  • Hermansky Pudlak Syndrome
                                                                                                                                                                    • AR Hyper IgM Syndrome
                                                                                                                                                                      • X-Linked Hyper IgM
                                                                                                                                                                        • ICF Syndrome
                                                                                                                                                                          • Interferon Gamma Pathway Defects
                                                                                                                                                                            • IgA Deficiency
                                                                                                                                                                              • IL10 & IL10 Receptor Deficiency
                                                                                                                                                                                • Incontinentia Pigmenti
                                                                                                                                                                                  • IPEX Syndrome
                                                                                                                                                                                    • IRAK4 Deficiency
                                                                                                                                                                                      • Kabuki Syndrome
                                                                                                                                                                                        • Leukocyte Adhesion Deficiency
                                                                                                                                                                                          • LRBA Deficiency
                                                                                                                                                                                            • Lysinuric Protein Intolerance
                                                                                                                                                                                              • MBL Deficiency
                                                                                                                                                                                                • Mevalonate Kinase Deficiency
                                                                                                                                                                                                  • MHC Class I Deficiency
                                                                                                                                                                                                    • MHC Class II Deficiency
                                                                                                                                                                                                      • Mulvihill Smith Syndrome
                                                                                                                                                                                                        • MYD88 Deficiency
                                                                                                                                                                                                          • Myotonic Dystrophy
                                                                                                                                                                                                            • NEMO
                                                                                                                                                                                                              • Netherton Syndrome
                                                                                                                                                                                                                • Nijmegen Breakage Syndrome
                                                                                                                                                                                                                  • Omenn Syndrome
                                                                                                                                                                                                                    • P14 Deficiency
                                                                                                                                                                                                                      • PAPA
                                                                                                                                                                                                                        • Papillon Lefevre Syndrome
                                                                                                                                                                                                                          • PIK3CD
                                                                                                                                                                                                                            • Poikiloderma with Neutropenia
                                                                                                                                                                                                                              • RAG1/RAG2 Deficiency
                                                                                                                                                                                                                                • Reticular Dysgenesis
                                                                                                                                                                                                                                  • Roifman Syndrome 1
                                                                                                                                                                                                                                    • Roifman Syndrome 2
                                                                                                                                                                                                                                      • Rubinstein-Taybi Syndrome
                                                                                                                                                                                                                                        • ADA SCID
                                                                                                                                                                                                                                          • Schimke Immuno-Osseous Dysplasia
                                                                                                                                                                                                                                            • SCID
                                                                                                                                                                                                                                              • CD3 COMPLEX DEFICIENCIES
                                                                                                                                                                                                                                                • CD45 DEFICIENCY
                                                                                                                                                                                                                                                  • IL7 SCID
                                                                                                                                                                                                                                                    • JAK3 SCID
                                                                                                                                                                                                                                                      • ORAM-STIM1 Deficiency
                                                                                                                                                                                                                                                        • PNP SCID
                                                                                                                                                                                                                                                          • X-Linked SCID
                                                                                                                                                                                                                                                            • Severe Congenital Neutropenia
                                                                                                                                                                                                                                                              • Shwachman Diamond Syndrome
                                                                                                                                                                                                                                                                • Specific Antibody Deficiency
                                                                                                                                                                                                                                                                  • STAT1 Gain of Function
                                                                                                                                                                                                                                                                    • STAT3 Gain of Function
                                                                                                                                                                                                                                                                      • AD Hyper IgE (STAT3 Deficiency)
                                                                                                                                                                                                                                                                        • STAT5B Deficiency
                                                                                                                                                                                                                                                                          • TLR3 Deficiency
                                                                                                                                                                                                                                                                            • Transcobalamin II
                                                                                                                                                                                                                                                                              • Transient Hypogammaglobinemia
                                                                                                                                                                                                                                                                                • TRAPS
                                                                                                                                                                                                                                                                                  • Trichohepatoenteric Syndrome
                                                                                                                                                                                                                                                                                    • Trisomy 21
                                                                                                                                                                                                                                                                                      • Turner Syndrome
                                                                                                                                                                                                                                                                                        • UNC-93B Deficiency
                                                                                                                                                                                                                                                                                          • WHIM Syndrome
                                                                                                                                                                                                                                                                                            • WHN Deficiency
                                                                                                                                                                                                                                                                                              • Wiskot-Aldrich Syndrome
                                                                                                                                                                                                                                                                                                • X-Linked Agammaglobulinemia
                                                                                                                                                                                                                                                                                                  • X-Linked Lymphoproliferative Syndrome
                                                                                                                                                                                                                                                                                                    • ZAP70 Deficiency
                                                                                                                                                                                                                                                                                                       
                                                                                                                                                                                                                                                                                                      DISEASE LIST