Disorder of immune structure

Code	`414030009`
Semantic tag	disorder
Module	international
Definition	defined
Effective time	20050131

234642007Age-related immunodeficiency disorder

234604001Alternative pathway deficiency disorder

1293264009Atypical haemolytic uraemic syndrome with complement gene abnormality disorder

702444009Autoimmune lymphoproliferative syndrome disorder

234534000Autosomal agammaglobulinaemia with absent B-cells disorder

1003473002B cell lymphocyte aplasia caused by drug disorder

234572005Benign combined immunodeficiency disorder

406565005CD4 T lymphocyte deficiency disorder

234633000Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency disorder

234634006Chromosome 18 syndromes and antibody deficiency disorder

234635007Chromosome 22 abnormalities with hypogammaglobulinaemia disorder

413835007Chronic disease of immune structure disorder

234593008Classical complement pathway abnormality disorder

766879006Combined immunodeficiency due to OX40 deficiency disorder

234547005Combined immunoglobulin G2 and G4 deficiency disorder

234591005Combined phagocytic defect disorder

191010004Common variable immunodeficiency disorder

234628004Complement receptor deficiency disorder

234618008Complement regulatory factor defect disorder

765327005Congenital sideroblastic anaemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome disorder

710027002Cytokine release syndrome disorder

234581004Defective phagocytic cell adhesion disorder

234580003Defective phagocytic cell chemotaxis disorder

234578009Defective phagocytic cell opsonisation disorder

840472009Deficiency of immunoglobulin A with immunoglobulin G subclass deficiency disorder

234637004Deletion of X-chromosome and hypogammaglobulinaemia disorder

417967008Disorder of eosinophil disorder

111590001Disorder of lymphoid system disorder

234645009Drug-induced immunodeficiency disorder

1141845003Eosinophilic microabscess of oesophagus disorder

1197483002Functional disorder of polymorphonuclear neutrophil disorder

234589002Glutathione synthetase deficiency disorder

234590006Gluthathione peroxidase deficiency disorder

234146006Hennekam syndrome disorder

1230414002Immune effector cell-associated neurotoxicity syndrome disorder

363142008Immune system complication of procedure disorder

766705006Immunodeficiency due to ficolin 3 deficiency disorder

191008001Immunodeficiency following hereditary defective response to Epstein-Barr virus disorder

234631003Immunodeficiency with major anomalies disorder

234551007Immunoglobulin A1 deficiency disorder

234552000Immunoglobulin A2 deficiency disorder

16894671000119102Immunoglobulin G deficiency due to monoclonal gammopathy of undetermined significance disorder

16894711000119103Immunoglobulin G deficiency due to multiple myeloma disorder

234550008Immunoglobulin G1 deficiency disorder

234546001Immunoglobulin G2 deficiency disorder

234548000Immunoglobulin G3 deficiency disorder

234549008Immunoglobulin G4 deficiency disorder

234539005Immunoglobulin heavy chain deficiency disorder

234543009Immunoglobulin light chain deficiency disorder

234553005Immunoglobulin-associated molecule deficiency disorder

109985000Immunoproliferative small intestinal disease (clinical) disorder

363161007Infectious disorder of immune system disorder

363177008Inflammatory disorder of immune system disorder

763668009Lichtenstein syndrome disorder

234577004Lipochrome histiocytosis - familial disorder

191018006Lymphocyte function antigen-1 defect disorder

68712004Lymphocytic hypoplasia disorder

118612006Malignant histiocytosis (clinical) disorder

397007003Mast cell disorder disorder

234638009Microcephaly, normal intelligence and immunodeficiency disorder

234433009Myeloperoxidase deficiency disorder

234588005Neutrophil secondary granule deficiency disorder

190808009Polyclonal hypergammaglobulinaemia disorder

234564008Primary immunoglobulin catabolism abnormality disorder

82546001Reactive immunoproliferative disease disorder

111584000Reticular dysgenesis disorder

190997006Severe combined immunodeficiency with low T- and B-cell numbers disorder

190998001Severe combined immunodeficiency with low or normal B-cell numbers disorder

234570002Severe combined immunodeficiency with maternofetal engraftment disorder

190996002Severe combined immunodeficiency with reticular dysgenesis disorder

1237618009Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome disorder

234556002Specific antibody deficiency disorder

765145001T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency disorder

234608003Terminal component deficiency disorder

363331007Traumatic injury of immune system disorder

234639001Triple X syndrome, epilepsy, and hypogammaglobulinaemia disorder

234584007Tuftsin deficiency disorder

234571003Warts, hypogammaglobulinaemia, infections, and myelokathexis disorder

65880007X-linked agammaglobulinaemia disorder

234533006X-linked agammaglobulinaemia with growth hormone deficiency disorder

719827008X-linked immunoneurologic disorder disorder

77121009X-linked lymphoproliferative syndrome disorder

Parents (1)

Children (82)