SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Congenital immunodeficiency disease  36138009

Severe combined immunodeficiency disease  31323000

Autosomal recessive SCID (severe combined immunodeficiency disease)  362993009

Autosomal recessive severe combined immunodeficiency   190993005

SNOMED CT code


SNOMED code190993005
nameAutosomal recessive severe combined immunodeficiency
statusremoved
date introduced2002-01-31
fully specified name(s)Autosomal recessive severe combined immunodeficiency (disorder)
synonyms
  • Autosomal recessive lymphopaenic agammaglobulinaemia
  • Autosomal recessive severe combined immunodeficiency
  • Autosomal recessive lymphopenic agammaglobulinemia
  • SCID - Autosomal recessive severe combined immunodeficiency
parentsAutosomal recessive SCID (severe combined immunodeficiency disease)   362993009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital immunodeficiency disease   36138009
          Severe combined immunodeficiency disease   31323000
            Autosomal recessive SCID (severe combined immunodeficiency disease)   362993009
              Autosomal recessive severe combined immunodeficiency   190993005  removed: 2022-05-31

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.

Access to this feature is available in the following products:
  • CPT® to SNOMED Crosswalks

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