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Disorder of immune structure 414030009 SNOMED CT code SNOMED code 414030009 name Disorder of immune structure status active date introduced 2005-01-31 fully specified name(s) Disorder of immune structure (disorder) synonyms Disorder of immune structure attributes - group1 Finding site Immune system structure 116003000 parents Disorder of body system 362965005 children Age-related immunodeficiency 234642007 Alternative pathway deficiency 234604001 Autosomal agammaglobulinemia with absent B-cells 234534000 Benign combined immunodeficiency 234572005 CD4 T lymphocyte deficiency 406565005 Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency 234633000 Chromosome 18 syndromes and antibody deficiency 234634006 Chromosome 22 abnormalities with hypogammaglobulinemia 234635007 Chronic disease of immune structure 413835007 Classical complement pathway abnormality 234593008 Combined immunodeficiency due to OX40 deficiency 766879006 Combined immunoglobulin G2 and G4 deficiency 234547005 Combined phagocytic defect 234591005 Common variable immunodeficiency with autoantibodies to B- or T-cells 191013002 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions 191011000 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders 191012007 Complement receptor deficiency 234628004 Complement regulatory factor defect 234618008 Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome 765327005 Constitutional mismatch repair deficiency syndrome 764946008 Defective phagocytic cell adhesion 234581004 Defective phagocytic cell chemotaxis 234580003 Defective phagocytic cell opsonization 234578009 Deletion of X-chromosome and hypogammaglobulinemia 234637004 Disorder of lymphoid system 111590001 Drug-induced immunodeficiency 234645009 Eosinophilic syndrome 5952007 removed: 2006-01-31 Functional disorders of polymorphonuclear neutrophils 267543009 Glutathione synthetase deficiency 234589002 Gluthathione peroxidase deficiency 234590006 Hennekam syndrome 234146006 Immune system complication of procedure 363142008 Immunodeficiency due to ficolin 3 deficiency 766705006 Immunodeficiency following hereditary defective response to Epstein-Barr virus 191008001 Immunodeficiency with major anomalies 234631003 Immunoglobulin A1 deficiency 234551007 Immunoglobulin A2 deficiency 234552000 Immunoglobulin G1 deficiency 234550008 Immunoglobulin G2 deficiency 234546001 Immunoglobulin G3 deficiency 234548000 Immunoglobulin G4 deficiency 234549008 Immunoglobulin heavy chain deficiency 234539005 Immunoglobulin light chain deficiency 234543009 Immunoglobulin-associated molecule deficiency 234553005 Immunoproliferative small intestinal disease (clinical) 109985000 Infectious disorder of immune system 363161007 Inflammatory disorder of immune system 363177008 Isolated agammaglobulinemia 764858009 Lichtenstein syndrome 763668009 Lipochrome histiocytosis - familial 234577004 Lymphocyte function antigen-1 defect 191018006 Major histocompatibility complex class I deficiency 191001007 Major histocompatibility complex class II deficiency 191002000 Malignant histiocytosis (clinical) 118612006 Mast cell disorder 397007003 Microcephaly, normal intelligence and immunodeficiency 234638009 Myeloperoxidase deficiency 234433009 Neutrophil secondary granule deficiency 234588005 Polyclonal hypergammaglobulinemia 190808009 Primary immunoglobulin catabolism abnormality 234564008 Reactive immunoproliferative disease 82546001 Reticular dysgenesis 111584000 Severe combined immunodeficiency with low or normal B-cell numbers 190998001 Severe combined immunodeficiency with low T- and B-cell numbers 190997006 Severe combined immunodeficiency with maternofetal engraftment 234570002 Severe combined immunodeficiency with reticular dysgenesis 190996002 Specific antibody deficiency 234556002 T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency 765145001 Terminal component deficiency 234608003 Traumatic injury of immune system 363331007 Triple X syndrome, epilepsy, and hypogammaglobulinemia 234639001 Tuftsin deficiency 234584007 Warts, hypogammaglobulinemia, infections, and myelokathexis 234571003 X-linked agammaglobulinemia with growth hormone deficiency 234533006 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 118234003 123946008 362965005 414030009 ancestors sorted most to least specific
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