Lichtenstein syndrome   763668009

SNOMED CT code


SNOMED code763668009
nameLichtenstein syndrome
statusactive
date introduced2018-07-31
fully specified name(s)Lichtenstein syndrome (disorder)
synonymsLichtenstein syndrome
attributes - group2
Pathological processAbnormal immune process   769247005
attributes - group1
Finding siteImmune system structure   116003000
OccurrenceCongenital   255399007
parents
  • Phagocytic cell dysfunction   302874002
  • Congenital immunodeficiency disease   36138009
  • Hereditary disorder of immune system   363138005
  • Disorder of immune structure   414030009
  • 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
            Phagocytic cell defect   234573000
              Phagocytic cell dysfunction   302874002
                Lichtenstein syndrome   763668009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital immunodeficiency disease   36138009
          Lichtenstein syndrome   763668009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of immune function   414029004
        Hereditary disorder of immune system   363138005
          Lichtenstein syndrome   763668009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of immune structure   414030009
          Lichtenstein syndrome   763668009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Lichtenstein syndrome   763668009

ancestors
sorted most to least specific
cpt crosswalks

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