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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 Blau syndrome 818950005 Combined immunodeficiency disease 442459007 Deficiency in anterior pituitary function, variable immunodeficiency syndrome 773664005 Deficiency of interleukin 36 receptor antagonist 784339002 Disorder of complement 24419001 Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome 771333006 Immunodeficiency associated with chromosomal abnormality 234632005 Immunodeficiency due to CD25 deficiency 778028008 Immunodeficiency with major anomalies 234631003 Immunoglobulin deficiency 417167007 Immunoglobulin heavy chain deficiency 234539005 Immunoglobulin light chain deficiency 234543009 Immunoglobulin-associated molecule deficiency 234553005 Interleukin-12 deficiency 449853003 Majeed syndrome 703540008 Mannose-binding lectin deficiency 703538003 MDA5 deficiency 768560008 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 Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection 783245001 Primary immunoglobulin catabolism abnormality 234564008 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 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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