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| 4752350514 | Chronic Granulomatous Disease | defect in the NADPH oxidase system | 0 | |
| 4752350515 | Myeloperoxidase Deficiency | deficiency in myeloperoxidase which is an important microbicidal agent in normal neutrophils | 1 | |
| 4752350516 | Chediak Higashi Syndrome | defect in gene encoding the lysosomal trafficking regulator protein | 2 | |
| 4752350517 | Job's Syndrome | neutrophils demonstrate defective chemotaxis but normal ingestion and killing | 3 | |
| 4752350518 | Lazy Leukocyte Syndrome | defective chemotactic response by neutrophils | 4 | |
| 4752350519 | Tuftsin Deficiency | tuftsin deficiency ehich is a phagocytosis-promoting serum tetrapeptide that is cleaved from an Ig like molecule, leukokinin, in the spleen | 5 | |
| 4752350520 | Leukocyte adhesion deficiency | leukocytes have defects of adhesion to endothelial surfaces and to each other as well as poor chemotactic and phagocytic activities | 6 | |
| 4752350521 | Bruton's Agammaglobulinemia | Genetic defect in long arm of X chromosome resulting in a block in the maturation of pre-B cells into lymphocytes with surface IgM | 7 | |
| 4752350522 | Dysgammaglobulinemia | suggested that an arrest in the development of the B cells in the culprit | 8 | |
| 4752350523 | Selective IgA deficiency | defect in class switching | 9 | |
| 4752350524 | Selective IgA deficiency | Most Common Immunodeficiency Disorder | 10 | |
| 4752350525 | Transient hypogammaglobulinemia of infancy | Onset of Ig synthesis | 11 | |
| 4752350526 | Digeorge syndrome | absence or hypoplasia of thymus and parathyroid glands | 12 | |
| 4752350527 | Chronic mucucutaneous candidiasis | T cells show an impaired ability to produce macrophage migration inhibiting factor (MIF) in response to candida antigen | 13 | |
| 4752350528 | Bare lymphocyte syndrome | deficiency in the expression of class II MHC gene products | 14 | |
| 4752350529 | Severe Combined Immunodeficiency disease (SCID) | combined defect in both humoral and cell mediated immunity | 15 | |
| 4752350530 | Nezelof's syndrome | Thymic dysplasia | 16 | |
| 4752350531 | Wiskott Aldrich Syndrome (WAS) | Mutation in WASP gene | 17 | |
| 4752350532 | Ataxia Telangiectasia | Result of specific genetic defect that affects DNA repair and alters the function of organ systems | 18 | |
| 4752350533 | X-Linked lymphoproliferative Disease or Duncan's syndrome | Mutation in SH2Dta/SAPaa gene resulting in weakening of both humoral and cell mediated immune response | 19 |
