Disorders of the Immune System (1450)    NLM VALUE SETS (802.2)

Name Value
NAME Disorders of the Immune System
OID 2.16.840.1.113883.3.464.1003.120.12.1001
SHORT ID DOTIS01
VERSION DATE 2017-01-06 00:00:00
CODE LIST
  • CODES:
    • CODE DESCRIPTION:   
      Severe combined immunodeficiency due to absent peripheral T cell maturation 
(disorder)
    • CODE DESCRIPTION:   
      Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)
    • CODE DESCRIPTION:   
      Acquired neutropenia in newborn (disorder)
    • CODE DESCRIPTION:   
      Cyclical neutropenia (disorder)
    • CODE DESCRIPTION:   
      X-linked severe combined immunodeficiency (disorder)
    • CODE DESCRIPTION:   
      X-linked hypogammaglobulinemia (disorder)
    • CODE DESCRIPTION:   
      Chronic benign neutropenia (disorder)
    • CODE DESCRIPTION:   
      Metabolic neutropenia (disorder)
    • CODE DESCRIPTION:   
      Autoimmune neutropenia (disorder)
    • CODE DESCRIPTION:   
      Corticosteroid-induced neutrophilia (disorder)
    • CODE DESCRIPTION:   
      Myeloperoxidase deficiency (disorder)
    • CODE DESCRIPTION:   
      Hemolytic erythrophagocytic syndrome (disorder)
    • CODE DESCRIPTION:   
      Common variable agammaglobulinemia (disorder)
    • CODE DESCRIPTION:   
      Hemophagocytic lymphohistiocytosis (disorder)
    • CODE DESCRIPTION:   
      Immunodeficiency disorder (disorder)
    • CODE DESCRIPTION:   
      X-linked agammaglobulinemia with growth hormone deficiency (disorder)
    • CODE DESCRIPTION:   
      Autosomal agammaglobulinemia with absent B-cells (disorder)
    • CODE DESCRIPTION:   
      Immunoglobulin heavy chain deficiency (disorder)
    • CODE DESCRIPTION:   
      Selective immunoglobulin E deficiency (disorder)
    • CODE DESCRIPTION:   
      Selective immunoglobulin D deficiency (disorder)
    • CODE DESCRIPTION:   
      Selective immunoglobulin M and immunoglobulin A deficiency (disorder)
    • CODE DESCRIPTION:   
      Immunoglobulin light chain deficiency (disorder)
    • CODE DESCRIPTION:   
      Immunoglobulin subclass deficiency (disorder)
    • CODE DESCRIPTION:   
      Aplasia of thymus gland with immunodeficiency (disorder)
    • CODE DESCRIPTION:   
      Immunoglobulin G2 deficiency (disorder)
    • CODE DESCRIPTION:   
      Combined immunoglobulin G2 and G4 deficiency (disorder)
    • CODE DESCRIPTION:   
      Immunoglobulin G3 deficiency (disorder)
    • CODE DESCRIPTION:   
      Immunoglobulin G4 deficiency (disorder)
    • CODE DESCRIPTION:   
      Immunoglobulin G1 deficiency (disorder)
    • CODE DESCRIPTION:   
      Immunoglobulin A1 deficiency (disorder)
    • CODE DESCRIPTION:   
      Immunoglobulin A2 deficiency (disorder)
    • CODE DESCRIPTION:   
      Immunoglobulin-associated molecule deficiency (disorder)
    • CODE DESCRIPTION:   
      Secretory piece deficiency (disorder)
    • CODE DESCRIPTION:   
      Defective immunoglobulin glycosylation (disorder)
    • CODE DESCRIPTION:   
      Disorder of complement (disorder)
    • CODE DESCRIPTION:   
      Specific antibody deficiency (disorder)
    • CODE DESCRIPTION:   
      Anti-polysaccharide antibody deficiency (disorder)
    • CODE DESCRIPTION:   
      Anti-haemophilus influenzae B polysaccharide antibody deficiency (disorder)
    • CODE DESCRIPTION:   
      Anti-pneumococcal polysaccharide antibody deficiency (disorder)
    • CODE DESCRIPTION:   
      Anti-meningococcal polysaccharide A antibody deficiency (disorder)
    • CODE DESCRIPTION:   
      Anti-meningococcal polysaccharide C antibody deficiency (disorder)
    • CODE DESCRIPTION:   
      Anti-protein antibody deficiency (disorder)
    • CODE DESCRIPTION:   
      Anti-staphylococcal antibody deficiency (disorder)
    • CODE DESCRIPTION:   
      Primary immunoglobulin catabolism abnormality (disorder)
    • CODE DESCRIPTION:   
      Immunoglobulin hypercatabolism (disorder)
    • CODE DESCRIPTION:   
      Complement deficiency disease (disorder)
    • CODE DESCRIPTION:   
      Familial immunoglobulin hypercatabolism (disorder)
    • CODE DESCRIPTION:   
      Severe combined immunodeficiency with maternofetal engraftment (disorder)
    • CODE DESCRIPTION:   
      Warts, hypogammaglobulinemia, infections, and myelokathexis (disorder)
    • CODE DESCRIPTION:   
      Benign combined immunodeficiency (disorder)
    • CODE DESCRIPTION:   
      Phagocytic cell defect (disorder)
    • CODE DESCRIPTION:   
      Disorder of phagocytic cell number (disorder)
    • CODE DESCRIPTION:   
      Chronic familial neutropenia (disorder)
    • CODE DESCRIPTION:   
      Lipochrome histiocytosis - familial (disorder)
    • CODE DESCRIPTION:   
      Defective phagocytic cell opsonization (disorder)
    • CODE DESCRIPTION:   
      Mannan-binding protein deficiency (disorder)
    • CODE DESCRIPTION:   
      Myelokathexis (disorder)
    • CODE DESCRIPTION:   
      Defective phagocytic cell chemotaxis (disorder)
    • CODE DESCRIPTION:   
      Defective phagocytic cell adhesion (disorder)
    • CODE DESCRIPTION:   
      Leukocyte adhesion deficiency - type 1 (disorder)
    • CODE DESCRIPTION:   
      Leukocyte adhesion deficiency - type 2 (disorder)
    • CODE DESCRIPTION:   
      Tuftsin deficiency (disorder)
    • CODE DESCRIPTION:   
      Defective phagocytic cell killing (disorder)
    • CODE DESCRIPTION:   
      Leukocyte glucose-6-phosphate dehydrogenase deficiency (disorder)
    • CODE DESCRIPTION:   
      Neutrophil lactoferrin deficiency (disorder)
    • CODE DESCRIPTION:   
      Neutrophil secondary granule deficiency (disorder)
    • CODE DESCRIPTION:   
      Glutathione synthetase deficiency (disorder)
    • CODE DESCRIPTION:   
      Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome (disorder)
    • CODE DESCRIPTION:   
      Gluthathione peroxidase deficiency (disorder)
    • CODE DESCRIPTION:   
      Combined phagocytic defect (disorder)
    • CODE DESCRIPTION:   
      Classical complement pathway abnormality (disorder)
    • CODE DESCRIPTION:   
      Complement 1q deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement 1q beta chain deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement 1q dysfunction (disorder)
    • CODE DESCRIPTION:   
      Complement 1r deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement 1s deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement 2 deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement 4 deficiency (disorder)
    • CODE DESCRIPTION:   
      Chronic granulomatous disease, type IIA (disorder)
    • CODE DESCRIPTION:   
      Complement 4A deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement 4B deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement 3 deficiency (disorder)
    • CODE DESCRIPTION:   
      Alternative pathway deficiency (disorder)
    • CODE DESCRIPTION:   
      Factor B deficiency (disorder)
    • CODE DESCRIPTION:   
      Factor D deficiency (disorder)
    • CODE DESCRIPTION:   
      Terminal component deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement 5 deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement 6 deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement 7 deficiency (disorder)
    • CODE DESCRIPTION:   
      Immunoglobulin A deficiency (disorder)
    • CODE DESCRIPTION:   
      Combined complement 6 and 7 deficiencies (disorder)
    • CODE DESCRIPTION:   
      Complement 8 beta chain deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement 8 beta chain dysfunction (disorder)
    • CODE DESCRIPTION:   
      Complement 8 alpha-gamma deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement 9 deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement regulatory factor defect (disorder)
    • CODE DESCRIPTION:   
      Hereditary C1 esterase inhibitor deficiency - deficient factor (disorder)
    • CODE DESCRIPTION:   
      Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder)
    • CODE DESCRIPTION:   
      Factor I deficiency (disorder)
    • CODE DESCRIPTION:   
      Factor H deficiency (disorder)
    • CODE DESCRIPTION:   
      Chronic granulomatous disease, type I (disorder)
    • CODE DESCRIPTION:   
      Complement 4 binding protein deficiency (disorder)
    • CODE DESCRIPTION:   
      Decay accelerating factor deficiency (disorder)
    • CODE DESCRIPTION:   
      Homologous restriction factor deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement 5a inhibitor deficiency (disorder)
    • CODE DESCRIPTION:   
      Anaphylotoxin inactivator deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement receptor deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement receptor 1 deficiency (disorder)
    • CODE DESCRIPTION:   
      Complement receptor 3 deficiency (disorder)
    • CODE DESCRIPTION:   
      Immunodeficiency with major anomalies (disorder)
    • CODE DESCRIPTION:   
      Immunodeficiency associated with chromosomal abnormality (disorder)
    • CODE DESCRIPTION:   
      Non dose-related drug-induced neutropenia (disorder)
    • CODE DESCRIPTION:   
      Severe combined immunodeficiency disease (disorder)
    • CODE DESCRIPTION:   
      Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency 
(disorder)
    • CODE DESCRIPTION:   
      Chromosome 18 syndromes and antibody deficiency (disorder)
    • CODE DESCRIPTION:   
      Chromosome 22 abnormalities with hypogammaglobulinemia (disorder)
    • CODE DESCRIPTION:   
      Monosomy 22 and absence of immunoglobulin A (disorder)
    • CODE DESCRIPTION:   
      Deletion of X-chromosome and hypogammaglobulinemia (disorder)
    • CODE DESCRIPTION:   
      Microcephaly, normal intelligence and immunodeficiency (disorder)
    • CODE DESCRIPTION:   
      Triple X syndrome, epilepsy, and hypogammaglobulinemia (disorder)
    • CODE DESCRIPTION:   
      18-p syndrome with associated immunodeficiency (disorder)
    • CODE DESCRIPTION:   
      Immunodeficiency associated with multiple organ system abnormalities (disorder)
    • CODE DESCRIPTION:   
      Age-related immunodeficiency (disorder)
    • CODE DESCRIPTION:   
      Toxic neutropenia (disorder)
    • CODE DESCRIPTION:   
      Transient immunodeficiency of infancy (disorder)
    • CODE DESCRIPTION:   
      Drug-induced immunodeficiency (disorder)
    • CODE DESCRIPTION:   
      Acquired C1 esterase inhibitor deficiency (disorder)
    • CODE DESCRIPTION:   
      Familial neutropenia (disorder)
    • CODE DESCRIPTION:   
      Chronic idiopathic neutropenia (disorder)
    • CODE DESCRIPTION:   
      Complement 5 dysfunction (disorder)
    • CODE DESCRIPTION:   
      Agranulocytopenic disorder (disorder)
    • CODE DESCRIPTION:   
      Neutropenia due to irradiation (disorder)
    • CODE DESCRIPTION:   
      Functional disorders of polymorphonuclear neutrophils (disorder)
    • CODE DESCRIPTION:   
      Chloramphenicol-induced neutropenia (disorder)
    • CODE DESCRIPTION:   
      Secondary immune deficiency disorder (disorder)
    • CODE DESCRIPTION:   
      Phagocytic cell dysfunction (disorder)
    • CODE DESCRIPTION:   
      Neutropenic disorder (disorder)
    • CODE DESCRIPTION:   
      De Vaal's syndrome (disorder)
    • CODE DESCRIPTION:   
      Reticular dysgenesis with congenital aleukocytosis (disorder)
    • CODE DESCRIPTION:   
      Acquired immunodeficiency syndrome with dermatomycosis (disorder)
    • CODE DESCRIPTION:   
      Autosomal recessive severe combined immunodeficiency disease (disorder)
    • CODE DESCRIPTION:   
      Complement component deficiency (disorder)
    • CODE DESCRIPTION:   
      Congenital immunodeficiency involving the hematopoietic system (disorder)
    • CODE DESCRIPTION:   
      Chronic granulomatous disease (disorder)
    • CODE DESCRIPTION:   
      Familial hemophagocytic lymphohistiocytosis (disorder)
    • CODE DESCRIPTION:   
      Wiskott-Aldrich syndrome (disorder)
    • CODE DESCRIPTION:   
      Immunodeficiency with multicarboxylase deficiency (disorder)
    • CODE DESCRIPTION:   
      B-lymphocyte immunodeficiency (disorder)
    • CODE DESCRIPTION:   
      T-lymphocyte immunodeficiency (disorder)
    • CODE DESCRIPTION:   
      Wiskott-Aldrich autosomal dominant variant syndrome (disorder)
    • CODE DESCRIPTION:   
      Febrile neutropenia (disorder)
    • CODE DESCRIPTION:   
      Neutrophilia (disorder)
    • CODE DESCRIPTION:   
      Neutropenia associated with acquired immunodeficiency syndrome (disorder)
    • CODE DESCRIPTION:   
      Immunoglobulin deficiency (disorder)
    • CODE DESCRIPTION:   
      Agranulocytosis associated with acquired immunodeficiency syndrome (disorder)
    • CODE DESCRIPTION:   
      Chemotherapy-induced neutropenia (disorder)
    • CODE DESCRIPTION:   
      Congenital immunodeficiency disease (disorder)
    • CODE DESCRIPTION:   
      Combined immunodeficiency disease (disorder)
    • CODE DESCRIPTION:   
      Severe combined immunodeficiency due to absent adenosine deaminase (disorder)
    • CODE DESCRIPTION:   
      Hypopigmentation-immunodeficiency disease (disorder)
    • CODE DESCRIPTION:   
      Familial C3B inhibitor deficiency syndrome (disorder)
    • CODE DESCRIPTION:   
      Chronic granulomatous disease, type IA (disorder)
    • CODE DESCRIPTION:   
      Neutropenia with dysgranulopoiesis (disorder)
    • CODE DESCRIPTION:   
      Bloom syndrome (disorder)
    • CODE DESCRIPTION:   
      Adenosine deaminase deficiency (disorder)
    • CODE DESCRIPTION:   
      Severe combined immunodeficiency due to absent interleukin-2 production 
(disorder)
    • CODE DESCRIPTION:   
      Kappa light chain disease (disorder)
    • CODE DESCRIPTION:   
      Neutropenia associated with infectious disease (disorder)
    • CODE DESCRIPTION:   
      Acute neutrophilia (disorder)
    • CODE DESCRIPTION:   
      Drug-induced neutropenia (disorder)
    • CODE DESCRIPTION:   
      Dysplasia of thymus gland with immunodeficiency (disorder)
    • CODE DESCRIPTION:   
      Severe combined immunodeficiency due to absent T cell receptor (disorder)
    • CODE DESCRIPTION:   
      Job's syndrome (disorder)
    • CODE DESCRIPTION:   
      Transient neonatal neutropenia (disorder)
    • CODE DESCRIPTION:   
      Immunoglobulinemia with isolated somatotropin deficiency (disorder)
    • CODE DESCRIPTION:   
      Nezelof's syndrome (disorder)
    • CODE DESCRIPTION:   
      Dose-related drug-induced neutropenia (disorder)
    • CODE DESCRIPTION:   
      Congenital hypergammaglobulinemia (disorder)
    • CODE DESCRIPTION:   
      Primary immune deficiency disorder (disorder)
    • CODE DESCRIPTION:   
      Purine-nucleoside phosphorylase deficiency (disorder)
    • CODE DESCRIPTION:   
      Acquired immune deficiency syndrome (disorder)
    • CODE DESCRIPTION:   
      Drug-induced neutrophilia (disorder)
    • CODE DESCRIPTION:   
      Immune neutropenia (disorder)
    • CODE DESCRIPTION:   
      X-linked agammaglobulinemia (disorder)
    • CODE DESCRIPTION:   
      Lambda light chain disease (disorder)
    • CODE DESCRIPTION:   
      Immunodeficiency with thymoma (disorder)
    • CODE DESCRIPTION:   
      Ataxia-telangiectasia syndrome (disorder)
    • CODE DESCRIPTION:   
      Pseudoneutrophilia (disorder)
    • CODE DESCRIPTION:   
      Lazy leukocyte syndrome (disorder)
    • CODE DESCRIPTION:   
      Neutrophilic leukemoid reaction (disorder)
    • CODE DESCRIPTION:   
      Severe combined immunodeficiency due to absent class II human leukocyte 
antigens (disorder)
    • CODE DESCRIPTION:   
      Agranulocytic angina (disorder)
    • CODE DESCRIPTION:   
      Chronic granulomatous disease, type IVA (disorder)
    • CODE DESCRIPTION:   
      Acquired immunodeficiency syndrome with Salmonella infection (disorder)
    • CODE DESCRIPTION:   
      X-linked lymphoproliferative syndrome (disorder)
    • CODE DESCRIPTION:   
      Chronic granulomatous disease, type II (disorder)
    • CODE DESCRIPTION:   
      Alloimmune neonatal neutropenia (disorder)
    • CODE DESCRIPTION:   
      Congenital leukocyte adherence deficiency (disorder)
    • CODE DESCRIPTION:   
      Isoimmune neutropenia (disorder)
    • CODE DESCRIPTION:   
      Chronic neutrophilia (disorder)
    • CODE DESCRIPTION:   
      Properdin deficiency disease (disorder)
    • CODE DESCRIPTION:   
      Hyperimmunoglobulin M syndrome (disorder)
    • CODE DESCRIPTION:   
      Chronic granulomatous disease, type III (disorder)
    • CODE DESCRIPTION:   
      Hereditary angioedema (disorder)
    • CODE DESCRIPTION:   
      Transient hypogammaglobulinemia of infancy (disorder)
    • CODE DESCRIPTION:   
      Shwachman syndrome (disorder)
    • CODE DESCRIPTION:   
      Congenital neutropenia (disorder)
    • CODE DESCRIPTION:   
      Agranulocytosis (disorder)
    • CODE DESCRIPTION:   
      Immunodeficiency secondary to neoplasm (disorder)
    • CODE DESCRIPTION:   
      Immunodeficiency secondary to trauma (disorder)
    • CODE DESCRIPTION:   
      Immunodeficiency secondary to corticosteroids (disorder)
    • CODE DESCRIPTION:   
      Immunodeficiency secondary to radiation therapy (disorder)
    • CODE DESCRIPTION:   
      Immunodeficiency secondary to chemotherapy (disorder)
    • CODE DESCRIPTION:   
      Quantitative disorder of neutrophils (disorder)
    • CODE DESCRIPTION:   
      Quantitative abnormality of granulocytes (disorder)
    • CODE DESCRIPTION:   
      Chdiak-Higashi syndrome (disorder)
    • CODE DESCRIPTION:   
      Reticular dysgenesis (disorder)
    • CODE DESCRIPTION:   
      Neutropenia associated with autoimmune disease (disorder)
    • CODE DESCRIPTION:   
      Complement abnormality (disorder)
    • CODE DESCRIPTION:   
      Severe combined immunodeficiency due to absent interleukin-2 receptor (disorder)
    • CODE DESCRIPTION:   
      Congenital agammaglobulinemia (disorder)
    • CODE DESCRIPTION:   
      Stress neutrophilia (disorder)
    • CODE DESCRIPTION:   
      Hereditary neutrophilia (disorder)
    • CODE DESCRIPTION:   
      Chronic benign neutropenia of childhood (disorder)
    • CODE DESCRIPTION:   
      Chronic idiopathic immunoneutropenia in adults (disorder)
    • CODE DESCRIPTION:   
      Chronic hypoplastic neutropenia (disorder)
    • CODE DESCRIPTION:   
      Selective immunoglobulin A deficiency (disorder)
    • CODE DESCRIPTION:   
      Selective immunoglobulin M deficiency (disorder)
    • CODE DESCRIPTION:   
      Selective immunoglobulin G deficiency (disorder)
    • CODE DESCRIPTION:   
      Chronic granulomatous disease, type IV (disorder)
    • CODE DESCRIPTION:   
      Autosomal recessive severe combined immunodeficiency (disorder)
    • CODE DESCRIPTION:   
      Thymic aplasia or dysplasia with immunodeficiency (disorder)
    • CODE DESCRIPTION:   
      Severe combined immunodeficiency with reticular dysgenesis (disorder)
    • CODE DESCRIPTION:   
      Severe combined immunodeficiency with low T- and B-cell numbers (disorder)
    • CODE DESCRIPTION:   
      Severe combined immunodeficiency with low or normal B-cell numbers (disorder)
    • CODE DESCRIPTION:   
      Major histocompatibility complex class I deficiency (disorder)
    • CODE DESCRIPTION:   
      Major histocompatibility complex class II deficiency (disorder)
    • CODE DESCRIPTION:   
      Immunodeficiency following hereditary defective response to Epstein-Barr 
virus (disorder)
    • CODE DESCRIPTION:   
      Lymphocyte function antigen-1 defect (disorder)
    • CODE DESCRIPTION:   
      Primary splenic neutropenia (disorder)
  • CODES:
    • CODE DESCRIPTION:   
      Selective IgA immunodeficiency
    • CODE DESCRIPTION:   
      Nezelof's syndrome
    • CODE DESCRIPTION:   
      Other deficiency of cell-mediated immunity
    • CODE DESCRIPTION:   
      Combined immunity deficiency
    • CODE DESCRIPTION:   
      Unspecified immunity deficiency
    • CODE DESCRIPTION:   
      Autoimmune lymphoproliferative syndrome
    • CODE DESCRIPTION:   
      Autoimmune disease, not elsewhere classified
    • CODE DESCRIPTION:   
      Acute graft-versus-host disease
    • CODE DESCRIPTION:   
      Chronic graft-versus-host disease
    • CODE DESCRIPTION:   
      Acute on chronic graft-versus-host disease
    • CODE DESCRIPTION:   
      Other specified disorders involving the immune mechanism
    • CODE DESCRIPTION:   
      Selective IgM immunodeficiency
    • CODE DESCRIPTION:   
      Unspecified disorder of immune mechanism
    • CODE:   279.00
      CODE DESCRIPTION:   
      Hypogammaglobulinemia, unspecified
    • CODE:   279.10
      CODE DESCRIPTION:   
      Immunodeficiency with predominant T-cell defect, unspecified
    • CODE:   279.50
      CODE DESCRIPTION:   
      Graft-versus-host disease, unspecified
    • CODE DESCRIPTION:   
      Other selective immunoglobulin deficiencies
    • CODE DESCRIPTION:   
      Congenital hypogammaglobulinemia
    • CODE DESCRIPTION:   
      Immunodeficiency with increased IgM
    • CODE DESCRIPTION:   
      Common variable immunodeficiency
    • CODE DESCRIPTION:   
      Other deficiency of humoral immunity
    • CODE DESCRIPTION:   
      Digeorge's syndrome
    • CODE DESCRIPTION:   
      Wiskott-aldrich syndrome
  • CODES:
    • CODE:   D80.0
      CODE DESCRIPTION:   
      Hereditary hypogammaglobulinemia
    • CODE:   D80.9
      CODE DESCRIPTION:   
      Immunodeficiency with predominantly antibody defects, unspecified
    • CODE:   D81.0
      CODE DESCRIPTION:   
      Severe combined immunodeficiency [SCID] with reticular dysgenesis
    • CODE:   D81.1
      CODE DESCRIPTION:   
      Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
    • CODE:   D81.2
      CODE DESCRIPTION:   
      Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
    • CODE:   D81.4
      CODE DESCRIPTION:   
      Nezelof's syndrome
    • CODE:   D81.6
      CODE DESCRIPTION:   
      Major histocompatibility complex class I deficiency
    • CODE:   D81.7
      CODE DESCRIPTION:   
      Major histocompatibility complex class II deficiency
    • CODE:   D81.89
      CODE DESCRIPTION:   
      Other combined immunodeficiencies
    • CODE:   D81.9
      CODE DESCRIPTION:   
      Combined immunodeficiency, unspecified
    • CODE:   D82.0
      CODE DESCRIPTION:   
      Wiskott-Aldrich syndrome
    • CODE:   D80.1
      CODE DESCRIPTION:   
      Nonfamilial hypogammaglobulinemia
    • CODE:   D82.1
      CODE DESCRIPTION:   
      Di George's syndrome
    • CODE:   D82.2
      CODE DESCRIPTION:   
      Immunodeficiency with short-limbed stature
    • CODE:   D82.3
      CODE DESCRIPTION:   
      Immunodeficiency following hereditary defective response to Epstein-Barr virus
    • CODE:   D82.4
      CODE DESCRIPTION:   
      Hyperimmunoglobulin E [IgE] syndrome
    • CODE:   D82.8
      CODE DESCRIPTION:   
      Immunodeficiency associated with other specified major defects
    • CODE:   D82.9
      CODE DESCRIPTION:   
      Immunodeficiency associated with major defect, unspecified
    • CODE:   D83.0
      CODE DESCRIPTION:   
      Common variable immunodeficiency with predominant abnormalities of B-cell 
numbers and function
    • CODE:   D83.1
      CODE DESCRIPTION:   
      Common variable immunodeficiency with predominant immunoregulatory T-cell 
disorders
    • CODE:   D83.2
      CODE DESCRIPTION:   
      Common variable immunodeficiency with autoantibodies to B- or T-cells
    • CODE:   D83.8
      CODE DESCRIPTION:   
      Other common variable immunodeficiencies
    • CODE:   D80.2
      CODE DESCRIPTION:   
      Selective deficiency of immunoglobulin A [IgA]
    • CODE:   D83.9
      CODE DESCRIPTION:   
      Common variable immunodeficiency, unspecified
    • CODE:   D84.0
      CODE DESCRIPTION:   
      Lymphocyte function antigen-1 [LFA-1] defect
    • CODE:   D84.1
      CODE DESCRIPTION:   
      Defects in the complement system
    • CODE:   D84.8
      CODE DESCRIPTION:   
      Other specified immunodeficiencies
    • CODE:   D84.9
      CODE DESCRIPTION:   
      Immunodeficiency, unspecified
    • CODE:   D89.3
      CODE DESCRIPTION:   
      Immune reconstitution syndrome
    • CODE:   D89.810
      CODE DESCRIPTION:   
      Acute graft-versus-host disease
    • CODE:   D89.811
      CODE DESCRIPTION:   
      Chronic graft-versus-host disease
    • CODE:   D89.812
      CODE DESCRIPTION:   
      Acute on chronic graft-versus-host disease
    • CODE:   D89.813
      CODE DESCRIPTION:   
      Graft-versus-host disease, unspecified
    • CODE:   D80.3
      CODE DESCRIPTION:   
      Selective deficiency of immunoglobulin G [IgG] subclasses
    • CODE:   D89.82
      CODE DESCRIPTION:   
      Autoimmune lymphoproliferative syndrome [ALPS]
    • CODE:   D89.89
      CODE DESCRIPTION:   
      Other specified disorders involving the immune mechanism, not elsewhere 
classified
    • CODE:   D89.9
      CODE DESCRIPTION:   
      Disorder involving the immune mechanism, unspecified
    • CODE:   D80.4
      CODE DESCRIPTION:   
      Selective deficiency of immunoglobulin M [IgM]
    • CODE:   D80.5
      CODE DESCRIPTION:   
      Immunodeficiency with increased immunoglobulin M [IgM]
    • CODE:   D80.6
      CODE DESCRIPTION:   
      Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
    • CODE:   D80.7
      CODE DESCRIPTION:   
      Transient hypogammaglobulinemia of infancy
    • CODE:   D80.8
      CODE DESCRIPTION:   
      Other immunodeficiencies with predominantly antibody defects
MEASURE LIST