SNOMED code 718230004 name Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency status active date introduced 2016-07-31 fully specified name(s) Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency (disorder) synonyms
  • Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete IFNgammaR1 deficiency
attributes - group2 Pathological process Abnormal immune process   769247005 attributes - group1 Due to Chromosomal disorder   409709004 parents
  • Immunodeficiency associated with chromosomal abnormality   234632005
  • Autosomal recessive hereditary disorder   85995004
hierarchies

a selection of possible paths

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of immune function   414029004
        Immunodeficiency disorder   234532001
          Primary immune deficiency disorder   58606001
            Immunodeficiency associated with chromosomal abnormality   234632005
              Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency   718230004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency   718230004

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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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