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Immunodeficiency associated with chromosomal abnormality 234632005 SNOMED CT code SNOMED code 234632005 name Immunodeficiency associated with chromosomal abnormality status active date introduced 2002-01-31 fully specified name(s) Immunodeficiency associated with chromosomal abnormality (disorder) synonyms Immunodeficiency associated with chromosomal abnormality attributes - group2 Pathological process Abnormal immune process 769247005 attributes - group1 Associated with Chromosomal disorder 409709004 parents Primary immune deficiency disorder 58606001 children Anhidrotic ectodermal dysplasia with immune deficiency 703525006 Ataxia-telangiectasia syndrome 68504005 Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome 722288007 Autoimmune lymphoproliferative syndrome with recurrent viral infection 722290008 Bloom syndrome 4434006 Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency 234633000 Chromosome 18 syndromes and antibody deficiency 234634006 Chromosome 22 abnormalities with hypogammaglobulinemia 234635007 Combined immunodeficiency due to OX40 deficiency 766879006 Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome 765327005 Constitutional mismatch repair deficiency syndrome 764946008 Deletion of X-chromosome and hypogammaglobulinemia 234637004 FADD-related immunodeficiency 723334006 Idiopathic CD4 lymphocytopenia 763713000 Immunodeficiency associated with 18p syndrome 234640004 Immunodeficiency due to ficolin 3 deficiency 766705006 Microcephaly, normal intelligence and immunodeficiency 234638009 Neutrophil immunodeficiency syndrome 723443003 Primary immunodeficiency syndrome due to p14 deficiency 718717004 Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency 724275005 Pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 718232007 RAS-associated autoimmune leukoproliferative disease 723508002 Triple X syndrome, epilepsy, and hypogammaglobulinemia 234639001 X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome 724276006 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 64572001 414029004 234532001 58606001 234632005 ancestors sorted most to least specific
cpt crosswalks Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.
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