Disorder of body system
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Disorder of immune structure (disorder)
Disorder of immune structure
aandoening van immuunsysteem
aandoening van afweersysteem
Id414030009
StatusDefined
Finding siteStructure of immune system
ICD-10 complex map reference set
TargetD89.9
RuleTRUE
AdviceALWAYS D89.9
CorrelationSNOMED CT source code to target map code correlation not specified
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Age-related immunodeficiency1
Alternative pathway deficiency3
Autoimmune lymphoproliferative syndrome2
Autosomal agammaglobulinemia with absent B-cells
B cell lymphocyte aplasia caused by drug
Benign combined immunodeficiency
CD4 T lymphocyte deficiency1
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency
Chromosome 18 syndromes and antibody deficiency
Chromosome 22 abnormalities with hypogammaglobulinemia1
Chronic disease of immune structure15
Classical complement pathway abnormality8
Combined immunodeficiency due to OX40 deficiency
Combined immunoglobulin G2 and G4 deficiency
Combined phagocytic defect3
Common variable immunodeficiency with autoantibodies to B- or T-cells
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
Complement receptor deficiency2
Complement regulatory factor defect12
Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome
Constitutional mismatch repair deficiency syndrome
Defective phagocytic cell adhesion1
Defective phagocytic cell chemotaxis2
Defective phagocytic cell opsonization1
Deficiency of immunoglobulin A with immunoglobulin G subclass deficiency
Deletion of X-chromosome and hypogammaglobulinemia
Disorder of eosinophil7
Disorder of lymphoid system10
Drug-induced immunodeficiency3
Functional disorder of polymorphonuclear neutrophil1
Glutathione synthetase deficiency
Gluthathione peroxidase deficiency
Hennekam syndrome
Immune effector cell-associated neurotoxicity syndrome
Immune system complication of procedure1
Immunodeficiency due to ficolin 3 deficiency
Immunodeficiency following hereditary defective response to Epstein-Barr virus
Immunodeficiency with major anomalies1
Immunoglobulin A1 deficiency
Immunoglobulin A2 deficiency
Immunoglobulin G deficiency due to monoclonal gammopathy of undetermined significance
Immunoglobulin G deficiency due to multiple myeloma
Immunoglobulin G1 deficiency
Immunoglobulin G2 deficiency
Immunoglobulin G3 deficiency
Immunoglobulin G4 deficiency
Immunoglobulin heavy chain deficiency6
Immunoglobulin light chain deficiency2
Immunoglobulin-associated molecule deficiency2
Immunoproliferative small intestinal disease (clinical)
Infectious disorder of immune system29
Inflammatory disorder of immune system11
Isolated agammaglobulinemia1
Lichtenstein syndrome
Lipochrome histiocytosis - familial
Lymphocyte function antigen-1 defect
Lymphocytic hypoplasia
Major histocompatibility complex class I deficiency
Major histocompatibility complex class II deficiency
Malignant histiocytosis (clinical)13
Mast cell disorder3
Microcephaly, normal intelligence and immunodeficiency
Myeloperoxidase deficiency
Neutrophil secondary granule deficiency
Polyclonal hypergammaglobulinemia
Primary immunoglobulin catabolism abnormality2
Reactive immunoproliferative disease1
Reticular dysgenesis2
Severe combined immunodeficiency with low or normal B-cell numbers
Severe combined immunodeficiency with low T- and B-cell numbers7
Severe combined immunodeficiency with maternofetal engraftment
Severe combined immunodeficiency with reticular dysgenesis
Specific antibody deficiency5
T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency
Terminal component deficiency8
Traumatic injury of immune system19
Triple X syndrome, epilepsy, and hypogammaglobulinemia
Tuftsin deficiency
Warts, hypogammaglobulinemia, infections, and myelokathexis
Well-differentiated systemic mastocytosis
X-linked agammaglobulinemia with growth hormone deficiency
X-linked immunoneurologic disorder
X-linked lymphoproliferative syndrome4