Hennekam syndrome   234146006

SNOMED CT code


SNOMED code234146006
nameHennekam syndrome
statusactive
date introduced2002-01-31
fully specified name(s)Hennekam lymphangiectasia-lymphedema syndrome (disorder)
synonyms
  • Hennekam lymphangiectasia-lymphoedema syndrome
  • Hennekam lymphangiectasia-lymphedema syndrome
  • Hennekam syndrome
  • Lymphoedema, lymphangiectasia, intellectual disability syndrome
  • Lymphedema, lymphangiectasia, intellectual disability syndrome
attributes - group1
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Associated morphologyLymphatic edema   30213001
Finding siteLimb structure   66019005
attributes - group2
Pathological processPathological developmental process   308490002
Finding siteLymphatics of intestinal structure   360980006
Associated morphologyLymphangiectasis   48087001
OccurrenceCongenital   255399007
attributes - group3
Associated morphologyMorphologically abnormal structure   49755003
Finding siteFace structure   89545001
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
attributes - group4
OccurrenceCongenital   255399007
Pathological processAbnormal immune process   769247005
Finding siteImmune system structure   116003000
attributes - group5
InterpretsIntellectual ability   247573007
Has interpretationImpaired   260379002
attributes - group6
InterpretsAdaptation behavior   406208005
Has interpretationImpaired   260379002
parents
  • Intellectual disability   110359009
  • Intestinal lymphangiectasis   197260007
  • Hereditary lymphedema   254199006
  • Congenital immunodeficiency disease   36138009
  • Congenital anomaly of lower trunk   363030001
  • Congenital anomaly of lymphatic structure of trunk   363031002
  • Hereditary disorder of immune system   363138005
  • Hereditary disorder of lymphatic system   363190001
  • Disorder of immune structure   414030009
  • Combined immunodeficiency disease   442459007
  • Congenital anomaly of limb   60475009
  • Multiple malformation syndrome with facial defects as major feature   65094009
  • Congenital lymphangiectasia   788292004
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Mental state, behavior and/or psychosocial function finding   384821006
      Behavior finding   844005
        Intellectual disability   110359009
          Hennekam syndrome   234146006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    General finding of soft tissue   248402002
      Disorder of soft tissue   19660004
        Soft tissue lesion   239953001
          Intestinal lymphangiectasis   197260007
            Hennekam syndrome   234146006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Primary lymphedema   1217009002
          Hereditary lymphedema   254199006
            Hennekam syndrome   234146006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital immunodeficiency disease   36138009
          Hennekam syndrome   234146006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of trunk structure   302292003
      Disorder of trunk   128121009
        Congenital anomaly of trunk   78626001
          Congenital anomaly of lower trunk   363030001
            Hennekam syndrome   234146006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of lymphatic system   362971004
          Congenital anomaly of lymphatic structure of trunk   363031002
            Hennekam syndrome   234146006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of immune function   414029004
        Hereditary disorder of immune system   363138005
          Hennekam syndrome   234146006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of lymphatic system   362971004
          Hereditary disorder of lymphatic system   363190001
            Hennekam syndrome   234146006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of immune structure   414030009
          Hennekam syndrome   234146006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of immune function   414029004
        Immunodeficiency disorder   234532001
          Primary immune deficiency disorder   58606001
            Combined immunodeficiency disease   442459007
              Hennekam syndrome   234146006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Disorder of limb   128605003
        Congenital anomaly of limb   60475009
          Hennekam syndrome   234146006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of head   118934005
        Disorder of face   118930001
          Congenital anomaly of face   398302004
            Multiple malformation syndrome with facial defects as major feature   65094009
              Hennekam syndrome   234146006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    General finding of soft tissue   248402002
      Disorder of soft tissue   19660004
        Soft tissue lesion   239953001
          Congenital lymphangiectasia   788292004
            Hennekam syndrome   234146006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Hennekam syndrome   234146006

ancestors
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