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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Congenital agammaglobulinemia 116133005 SNOMED CT code SNOMED code 116133005 name Congenital agammaglobulinemia status active date introduced 2002-01-31 fully specified name(s) Congenital agammaglobulinemia (disorder) synonyms Congenital agammaglobulinemia Congenital agammaglobulinaemia attributes - group2 Pathological process Abnormal immune process 769247005 attributes - group1 Occurrence Congenital 255399007 parents Congenital immunodeficiency disease 36138009 children Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome 722281001 Autosomal agammaglobulinemia with absent B-cells 234534000 B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome 1230295000 Isolated agammaglobulinemia 764858009 SCID (severe combined immunodeficiency) due to absent lymphoid stem cells 22406001 X-linked agammaglobulinemia with growth hormone deficiency 234533006 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 64572001 66091009 36138009 116133005 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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