CPT Changes Current book and archives back to 2000 Easy-to-read online book format Linked to and from code details
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Primary immune deficiency disorder 58606001 SNOMED CT code SNOMED code 58606001 name Primary immune deficiency disorder status active date introduced 2002-01-31 fully specified name(s) Primary immune deficiency disorder (disorder) synonyms Primary immunodeficiency Primary immune deficiency disorder attributes - group1 Pathological process Abnormal immune process 769247005 parents Immunodeficiency disorder 234532001 children Activated PI3K-delta syndrome 711480000 Autoimmune lymphoproliferative syndrome 702444009 Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity 1197366007 Blau syndrome 818950005 CEBPE-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome 1186720006 Combined immunodeficiency disease 442459007 Common variable immunodeficiency 191010004 Deficiency in anterior pituitary function, variable immunodeficiency syndrome 773664005 Deficiency of interleukin 36 receptor antagonist 784339002 Disorder of complement 24419001 Disorder of immunoglobulin 124950009 IL21-related infantile inflammatory bowel disease 1173999006 Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome 771333006 Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome 1186654001 Immunodeficiency associated with chromosomal abnormality 234632005 Immunodeficiency due to CD25 deficiency 778028008 Immunodeficiency with major anomalies 234631003 Immunoglobulin deficiency 417167007 removed: 2023-03-31 Immunoglobulin heavy chain deficiency 234539005 Immunoglobulin light chain deficiency 234543009 Immunoglobulin-associated molecule deficiency 234553005 Infantile inflammatory bowel disease with neurological involvement 1186721005 Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia 1197476009 Inflammatory bowel disease, recurrent sinopulmonary infection syndrome 1186652002 Interleukin-12 deficiency 449853003 Isolated agammaglobulinemia 764858009 Majeed syndrome 703540008 Mannose-binding lectin deficiency 703538003 MDA5 deficiency 768560008 Mendelian susceptibility to mycobacterial disease 1172895006 Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome 721903007 Neonatal inflammatory skin and bowel disease 773662009 Phagocytic cell defect 234573000 PLCG2-associated antibody deficiency and immune dysregulation 773646003 Predisposition to invasive fungal disease due to CARD9 deficiency 1186719000 Predisposition to severe viral infection due to IRF7 deficiency 1269234000 Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection 783245001 Primary immunoglobulin catabolism abnormality 234564008 Pyogenic arthritis, pyoderma gangrenosum, acne syndrome 724015007 Specific antibody deficiency 234556002 Sterile multifocal osteomyelitis with periostitis and pustulosis 773702002 Susceptibility to viral and mycobacterial infection 778045003 Syndromic multisystem autoimmune disease due to ITCH deficiency 778023004 T-cell immunodeficiency with epidermodysplasia verruciformis 770785002 Tuftsin deficiency 234584007 Vasculitis due to adenosine deaminase 2 deficiency 770687001 Warts, immunodeficiency, lymphedema, anogenital dysplasia syndrome 1186725001 X-linked immunoneurologic disorder 719827008 X-linked lymphoproliferative syndrome 77121009 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 64572001 414029004 234532001 58606001 ancestors sorted most to least specific
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