Severe combined immunodeficiency disease 31323000 SNOMED CT code SNOMED code 31323000 name Severe combined immunodeficiency disease status active date introduced 2002-01-31 fully specified name(s) Severe combined immunodeficiency disease (disorder) synonyms Severe combined immunodeficiency Combined T-cell and B-cell immunodeficiency Severe combined immunodeficiency disease SCID - severe combined immunodeficiency attributes - group3 Pathological process Abnormal immune process 769247005 attributes - group2 Finding site Body system structure 91689009 attributes - group1 Occurrence Congenital 255399007 parents Congenital immunodeficiency disease 36138009 Hereditary disorder of immune system 363138005 Combined immunodeficiency disease 442459007 children Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome 720986005 Autosomal recessive SCID (severe combined immunodeficiency disease) 362993009 Combined immunity deficiency NOS 191003005 removed: 2010-01-31 Major histocompatibility complex class I deficiency 191001007 Major histocompatibility complex class II deficiency 191002000 Nezelof's syndrome 55602000 SCID (severe combined immunodeficiency) due to absent adenosine deaminase 36980009 SCID (severe combined immunodeficiency) due to absent class II HLA (human leukocyte antigens) 71904008 SCID (severe combined immunodeficiency) due to absent IL-2 (interleukin-2) production 45390000 SCID (severe combined immunodeficiency) due to absent lymphoid stem cells 22406001 SCID (severe combined immunodeficiency) due to absent peripheral T cell maturation 3439009 SCID (severe combined immunodeficiency) due to absent T cell receptor 49555001 SCID due to absent IL-2 receptor 111587007 Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency 716871006 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 T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency 765145001 Warts, hypogammaglobulinemia, infections, and myelokathexis 234571003 X-linked severe combined immunodeficiency 203592006 removed: 2018-07-31 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 64572001 66091009 36138009 31323000 138875005 404684003 64572001 414029004 363138005 31323000 138875005 404684003 64572001 414029004 234532001 58606001 442459007 31323000 ancestors sorted most to least specific
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