Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)
Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)
Acquired neutropenia in newborn (disorder)
Cyclical neutropenia (disorder)
X-linked severe combined immunodeficiency (disorder)
X-linked hypogammaglobulinemia (disorder)
Chronic benign neutropenia (disorder)
Metabolic neutropenia (disorder)
Autoimmune neutropenia (disorder)
Corticosteroid-induced neutrophilia (disorder)
Myeloperoxidase deficiency (disorder)
Hemolytic erythrophagocytic syndrome (disorder)
Common variable agammaglobulinemia (disorder)
Hemophagocytic lymphohistiocytosis (disorder)
Immunodeficiency disorder (disorder)
X-linked agammaglobulinemia with growth hormone deficiency (disorder)
Autosomal agammaglobulinemia with absent B-cells (disorder)
Immunoglobulin heavy chain deficiency (disorder)
Selective immunoglobulin E deficiency (disorder)
Selective immunoglobulin D deficiency (disorder)
Selective immunoglobulin M and immunoglobulin A deficiency (disorder)
Immunoglobulin light chain deficiency (disorder)
Immunoglobulin subclass deficiency (disorder)
Aplasia of thymus gland with immunodeficiency (disorder)
Immunoglobulin G2 deficiency (disorder)
Combined immunoglobulin G2 and G4 deficiency (disorder)
Immunoglobulin G3 deficiency (disorder)
Immunoglobulin G4 deficiency (disorder)
Immunoglobulin G1 deficiency (disorder)
Immunoglobulin A1 deficiency (disorder)
Immunoglobulin A2 deficiency (disorder)
Immunoglobulin-associated molecule deficiency (disorder)
Secretory piece deficiency (disorder)
Defective immunoglobulin glycosylation (disorder)
Disorder of complement (disorder)
Specific antibody deficiency (disorder)
Anti-polysaccharide antibody deficiency (disorder)
Anti-haemophilus influenzae B polysaccharide antibody deficiency (disorder)
Anti-pneumococcal polysaccharide antibody deficiency (disorder)
Anti-meningococcal polysaccharide A antibody deficiency (disorder)
Anti-meningococcal polysaccharide C antibody deficiency (disorder)
Anti-protein antibody deficiency (disorder)
Anti-staphylococcal antibody deficiency (disorder)
Primary immunoglobulin catabolism abnormality (disorder)
Immunoglobulin hypercatabolism (disorder)
Complement deficiency disease (disorder)
Familial immunoglobulin hypercatabolism (disorder)
Severe combined immunodeficiency with maternofetal engraftment (disorder)
Warts, hypogammaglobulinemia, infections, and myelokathexis (disorder)
Benign combined immunodeficiency (disorder)
Phagocytic cell defect (disorder)
Disorder of phagocytic cell number (disorder)
Chronic familial neutropenia (disorder)
Lipochrome histiocytosis - familial (disorder)
Defective phagocytic cell opsonization (disorder)
Mannan-binding protein deficiency (disorder)
Myelokathexis (disorder)
Defective phagocytic cell chemotaxis (disorder)
Defective phagocytic cell adhesion (disorder)
Leukocyte adhesion deficiency - type 1 (disorder)
Leukocyte adhesion deficiency - type 2 (disorder)
Tuftsin deficiency (disorder)
Defective phagocytic cell killing (disorder)
Leukocyte glucose-6-phosphate dehydrogenase deficiency (disorder)
Neutrophil lactoferrin deficiency (disorder)
Neutrophil secondary granule deficiency (disorder)
Glutathione synthetase deficiency (disorder)
Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome (disorder)
Gluthathione peroxidase deficiency (disorder)
Combined phagocytic defect (disorder)
Classical complement pathway abnormality (disorder)
Complement 1q deficiency (disorder)
Complement 1q beta chain deficiency (disorder)
Complement 1q dysfunction (disorder)
Complement 1r deficiency (disorder)
Complement 1s deficiency (disorder)
Complement 2 deficiency (disorder)
Complement 4 deficiency (disorder)
Chronic granulomatous disease, type IIA (disorder)
Complement 4A deficiency (disorder)
Complement 4B deficiency (disorder)
Complement 3 deficiency (disorder)
Alternative pathway deficiency (disorder)
Factor B deficiency (disorder)
Factor D deficiency (disorder)
Terminal component deficiency (disorder)
Complement 5 deficiency (disorder)
Complement 6 deficiency (disorder)
Complement 7 deficiency (disorder)
Immunoglobulin A deficiency (disorder)
Combined complement 6 and 7 deficiencies (disorder)
Complement 8 beta chain deficiency (disorder)
Complement 8 beta chain dysfunction (disorder)
Complement 8 alpha-gamma deficiency (disorder)
Complement 9 deficiency (disorder)
Complement regulatory factor defect (disorder)
Hereditary C1 esterase inhibitor deficiency - deficient factor (disorder)
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder)
Factor I deficiency (disorder)
Factor H deficiency (disorder)
Chronic granulomatous disease, type I (disorder)
Complement 4 binding protein deficiency (disorder)
Decay accelerating factor deficiency (disorder)
Homologous restriction factor deficiency (disorder)
Complement 5a inhibitor deficiency (disorder)
Anaphylotoxin inactivator deficiency (disorder)
Complement receptor deficiency (disorder)
Complement receptor 1 deficiency (disorder)
Complement receptor 3 deficiency (disorder)
Immunodeficiency with major anomalies (disorder)
Immunodeficiency associated with chromosomal abnormality (disorder)
Non dose-related drug-induced neutropenia (disorder)
Severe combined immunodeficiency disease (disorder)
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency (disorder)
Chromosome 18 syndromes and antibody deficiency (disorder)
Chromosome 22 abnormalities with hypogammaglobulinemia (disorder)
Monosomy 22 and absence of immunoglobulin A (disorder)
Deletion of X-chromosome and hypogammaglobulinemia (disorder)
Microcephaly, normal intelligence and immunodeficiency (disorder)
Triple X syndrome, epilepsy, and hypogammaglobulinemia (disorder)
18-p syndrome with associated immunodeficiency (disorder)
Immunodeficiency associated with multiple organ system abnormalities (disorder)
Age-related immunodeficiency (disorder)
Toxic neutropenia (disorder)
Transient immunodeficiency of infancy (disorder)
Drug-induced immunodeficiency (disorder)
Acquired C1 esterase inhibitor deficiency (disorder)
Familial neutropenia (disorder)
Chronic idiopathic neutropenia (disorder)
Complement 5 dysfunction (disorder)
Agranulocytopenic disorder (disorder)
Neutropenia due to irradiation (disorder)
Functional disorders of polymorphonuclear neutrophils (disorder)
Chloramphenicol-induced neutropenia (disorder)
Secondary immune deficiency disorder (disorder)
Phagocytic cell dysfunction (disorder)
Neutropenic disorder (disorder)
De Vaal's syndrome (disorder)
Reticular dysgenesis with congenital aleukocytosis (disorder)
Acquired immunodeficiency syndrome with dermatomycosis (disorder)
Autosomal recessive severe combined immunodeficiency disease (disorder)
Complement component deficiency (disorder)
Congenital immunodeficiency involving the hematopoietic system (disorder)
Chronic granulomatous disease (disorder)
Familial hemophagocytic lymphohistiocytosis (disorder)
Wiskott-Aldrich syndrome (disorder)
Immunodeficiency with multicarboxylase deficiency (disorder)
B-lymphocyte immunodeficiency (disorder)
T-lymphocyte immunodeficiency (disorder)
Wiskott-Aldrich autosomal dominant variant syndrome (disorder)
Febrile neutropenia (disorder)
Neutrophilia (disorder)
Neutropenia associated with acquired immunodeficiency syndrome (disorder)
Immunoglobulin deficiency (disorder)
Agranulocytosis associated with acquired immunodeficiency syndrome (disorder)
Chemotherapy-induced neutropenia (disorder)
Congenital immunodeficiency disease (disorder)
Combined immunodeficiency disease (disorder)
Severe combined immunodeficiency due to absent adenosine deaminase (disorder)
Hypopigmentation-immunodeficiency disease (disorder)
Familial C3B inhibitor deficiency syndrome (disorder)
Chronic granulomatous disease, type IA (disorder)
Neutropenia with dysgranulopoiesis (disorder)
Bloom syndrome (disorder)
Adenosine deaminase deficiency (disorder)
Severe combined immunodeficiency due to absent interleukin-2 production (disorder)
Kappa light chain disease (disorder)
Neutropenia associated with infectious disease (disorder)
Acute neutrophilia (disorder)
Drug-induced neutropenia (disorder)
Dysplasia of thymus gland with immunodeficiency (disorder)
Severe combined immunodeficiency due to absent T cell receptor (disorder)
Job's syndrome (disorder)
Transient neonatal neutropenia (disorder)
Immunoglobulinemia with isolated somatotropin deficiency (disorder)
Nezelof's syndrome (disorder)
Dose-related drug-induced neutropenia (disorder)
Congenital hypergammaglobulinemia (disorder)
Primary immune deficiency disorder (disorder)
Purine-nucleoside phosphorylase deficiency (disorder)
Acquired immune deficiency syndrome (disorder)
Drug-induced neutrophilia (disorder)
Immune neutropenia (disorder)
X-linked agammaglobulinemia (disorder)
Lambda light chain disease (disorder)
Immunodeficiency with thymoma (disorder)
Ataxia-telangiectasia syndrome (disorder)
Pseudoneutrophilia (disorder)
Lazy leukocyte syndrome (disorder)
Neutrophilic leukemoid reaction (disorder)
Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)
Agranulocytic angina (disorder)
Chronic granulomatous disease, type IVA (disorder)
Acquired immunodeficiency syndrome with Salmonella infection (disorder)
X-linked lymphoproliferative syndrome (disorder)
Chronic granulomatous disease, type II (disorder)
Alloimmune neonatal neutropenia (disorder)
Congenital leukocyte adherence deficiency (disorder)
Isoimmune neutropenia (disorder)
Chronic neutrophilia (disorder)
Properdin deficiency disease (disorder)
Hyperimmunoglobulin M syndrome (disorder)
Chronic granulomatous disease, type III (disorder)
Hereditary angioedema (disorder)
Transient hypogammaglobulinemia of infancy (disorder)
Shwachman syndrome (disorder)
Congenital neutropenia (disorder)
Agranulocytosis (disorder)
Immunodeficiency secondary to neoplasm (disorder)
Immunodeficiency secondary to trauma (disorder)
Immunodeficiency secondary to corticosteroids (disorder)
Immunodeficiency secondary to radiation therapy (disorder)
Immunodeficiency secondary to chemotherapy (disorder)
Quantitative disorder of neutrophils (disorder)
Quantitative abnormality of granulocytes (disorder)
Chdiak-Higashi syndrome (disorder)
Reticular dysgenesis (disorder)
Neutropenia associated with autoimmune disease (disorder)
Complement abnormality (disorder)
Severe combined immunodeficiency due to absent interleukin-2 receptor (disorder)
Congenital agammaglobulinemia (disorder)
Stress neutrophilia (disorder)
Hereditary neutrophilia (disorder)
Chronic benign neutropenia of childhood (disorder)
Chronic idiopathic immunoneutropenia in adults (disorder)
Chronic hypoplastic neutropenia (disorder)
Selective immunoglobulin A deficiency (disorder)
Selective immunoglobulin M deficiency (disorder)
Selective immunoglobulin G deficiency (disorder)
Chronic granulomatous disease, type IV (disorder)
Autosomal recessive severe combined immunodeficiency (disorder)
Thymic aplasia or dysplasia with immunodeficiency (disorder)
Severe combined immunodeficiency with reticular dysgenesis (disorder)
Severe combined immunodeficiency with low T- and B-cell numbers (disorder)
Severe combined immunodeficiency with low or normal B-cell numbers (disorder)
Major histocompatibility complex class I deficiency (disorder)
Major histocompatibility complex class II deficiency (disorder)
Immunodeficiency following hereditary defective response to Epstein-Barr virus (disorder)
Lymphocyte function antigen-1 defect (disorder)
Primary splenic neutropenia (disorder)
Selective IgA immunodeficiency
Nezelof's syndrome
Other deficiency of cell-mediated immunity
Combined immunity deficiency
Unspecified immunity deficiency
Autoimmune lymphoproliferative syndrome
Autoimmune disease, not elsewhere classified
Acute graft-versus-host disease
Chronic graft-versus-host disease
Acute on chronic graft-versus-host disease
Other specified disorders involving the immune mechanism
Selective IgM immunodeficiency
Unspecified disorder of immune mechanism
Hypogammaglobulinemia, unspecified
Immunodeficiency with predominant T-cell defect, unspecified
Graft-versus-host disease, unspecified
Other selective immunoglobulin deficiencies
Congenital hypogammaglobulinemia
Immunodeficiency with increased IgM
Common variable immunodeficiency
Other deficiency of humoral immunity
Digeorge's syndrome
Wiskott-aldrich syndrome
Hereditary hypogammaglobulinemia
Immunodeficiency with predominantly antibody defects, unspecified
Severe combined immunodeficiency [SCID] with reticular dysgenesis
Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
Major histocompatibility complex class I deficiency
Major histocompatibility complex class II deficiency
Other combined immunodeficiencies
Combined immunodeficiency, unspecified
Wiskott-Aldrich syndrome
Nonfamilial hypogammaglobulinemia
Di George's syndrome
Immunodeficiency with short-limbed stature
Immunodeficiency following hereditary defective response to Epstein-Barr virus
Hyperimmunoglobulin E [IgE] syndrome
Immunodeficiency associated with other specified major defects
Immunodeficiency associated with major defect, unspecified
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
Common variable immunodeficiency with autoantibodies to B- or T-cells
Other common variable immunodeficiencies
Selective deficiency of immunoglobulin A [IgA]
Common variable immunodeficiency, unspecified
Lymphocyte function antigen-1 [LFA-1] defect
Defects in the complement system
Other specified immunodeficiencies
Immunodeficiency, unspecified
Immune reconstitution syndrome
Selective deficiency of immunoglobulin G [IgG] subclasses
Autoimmune lymphoproliferative syndrome [ALPS]
Other specified disorders involving the immune mechanism, not elsewhere classified
Disorder involving the immune mechanism, unspecified
Selective deficiency of immunoglobulin M [IgM]
Immunodeficiency with increased immunoglobulin M [IgM]
Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
Transient hypogammaglobulinemia of infancy
Other immunodeficiencies with predominantly antibody defects
