SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Disorder of body system  362965005

Disorder of immune structure  414030009

Severe combined immunodeficiency with low T- and B-cell numbers  190997006

Severe combined immunodeficiency with hypereosinophilia   722067005

SNOMED CT code


SNOMED code722067005
nameSevere combined immunodeficiency with hypereosinophilia
statusactive
date introduced2017-01-31
fully specified name(s)Severe combined immunodeficiency with hypereosinophilia (disorder)
synonyms
  • Severe combined immunodeficiency with hypereosinophilia
  • Omenn syndrome
attributes - group2
Pathological processAbnormal immune process   769247005
Finding siteEosinophilic granulocytic cell   127916009
attributes - group3
OccurrenceCongenital   255399007
Finding siteImmune system structure   116003000
attributes - group1
Has interpretationAbove reference range   281302008
InterpretsEosinophil count   71960002
parents
  • Severe combined immunodeficiency with low T- and B-cell numbers   190997006
  • Hereditary eosinophilia   191358004
  • Autosomal recessive SCID (severe combined immunodeficiency disease)   362993009
  • Disorder of eosinophil   417967008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of immune structure   414030009
          Severe combined immunodeficiency with low T- and B-cell numbers   190997006
            Severe combined immunodeficiency with hypereosinophilia   722067005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of blood, lymphatics and immune system   299691001
      Disorder of cellular component of blood   414022008
        White blood cell disorder   54097007
          Hereditary white blood cell disorder   414395005
            Hereditary eosinophilia   191358004
              Severe combined immunodeficiency with hypereosinophilia   722067005

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
              Severe combined immunodeficiency with hypereosinophilia   722067005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of immune structure   414030009
          Disorder of eosinophil   417967008
            Severe combined immunodeficiency with hypereosinophilia   722067005

ancestors
sorted most to least specific
  • Severe combined immunodeficiency with low T- and B-cell numbers   190997006
  • Hereditary eosinophilia   191358004
  • Autosomal recessive SCID (severe combined immunodeficiency disease)   362993009
  • Disorder of eosinophil   417967008
  • Severe combined immunodeficiency disease   31323000
  • Hereditary white blood cell disorder   414395005
  • Disorder of immune structure   414030009
  • Disorder characterized by eosinophilia   419455006
  • Autosomal recessive hereditary disorder   85995004
  • Congenital immunodeficiency disease   36138009
  • Hereditary disorder of immune system   363138005
  • Combined immunodeficiency disease   442459007
  • Leukocytosis   111583006
  • Hereditary disorder of cellular element of blood   414393003
  • Autosomal hereditary disorder   1899006
  • Eosinophil count above reference range   386789004
  • Hereditary disorder by system   363137000
  • Primary immune deficiency disorder   58606001
  • Congenital disease   66091009
  • White blood cell disorder   54097007
  • Granulocyte count above reference range   1157254007
  • Eosinophil count - finding   365601007
  • Immunodeficiency disorder   234532001
  • Hereditary disease   32895009
  • Disorder of body system   362965005
  • Blood leukocyte number above reference range   414478003
  • Disorder of cellular component of blood   414022008
  • Disorder of immune function   414029004
  • Genetic disease   782964007
  • White blood cell count outside reference range   165509000
  • Finding of blood, lymphatics and immune system   299691001
  • Measurement finding above reference range   442756004
  • Disease   64572001
  • White blood cell number - finding   365630000
  • Blood cell count outside reference range   762656009
  • Measurement finding outside reference range   442096005
  • Measurement finding   118245000
  • Evaluation finding   441742003
  • Procedure related finding   127325009
  • Clinical finding   404684003
  • SNOMED CT Concept   138875005
cpt crosswalks

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