Aplasia cutis congenita with intestinal lymphangiectasia syndrome   720500008

SNOMED CT code


SNOMED code720500008
nameAplasia cutis congenita with intestinal lymphangiectasia syndrome
statusactive
date introduced2017-01-31
fully specified name(s)Aplasia cutis congenita with intestinal lymphangiectasia syndrome (disorder)
synonyms
  • Aplasia cutis congenita with intestinal lymphangiectasia syndrome
  • Bronspiegel Zelnick syndrome
attributes - group1
OccurrenceCongenital   255399007
Associated morphologyLymphangiectasis   48087001
Pathological processPathological developmental process   308490002
Finding siteLymphatics of intestinal structure   360980006
attributes - group2
Pathological processPathological developmental process   308490002
Associated morphologyAplasia   45486003
OccurrenceCongenital   255399007
Finding siteSkin part   119181002
parents
  • Intestinal lymphangiectasis   197260007
  • Aplasia cutis congenita   35484002
  • Congenital anomaly of lower trunk   363030001
  • Congenital anomaly of lymphatic structure of trunk   363031002
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of the integument   363185004
  • Hereditary disorder of lymphatic system   363190001
  • Congenital lymphangiectasia   788292004
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
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
            Aplasia cutis congenita with intestinal lymphangiectasia syndrome   720500008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Congenital anomaly of integument   38164009
          Congenital anomaly of skin   199879009
            Aplasia cutis congenita   35484002
              Aplasia cutis congenita with intestinal lymphangiectasia syndrome   720500008

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
            Aplasia cutis congenita with intestinal lymphangiectasia syndrome   720500008

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
            Aplasia cutis congenita with intestinal lymphangiectasia syndrome   720500008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Aplasia cutis congenita with intestinal lymphangiectasia syndrome   720500008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Hereditary disorder of the integument   363185004
          Aplasia cutis congenita with intestinal lymphangiectasia syndrome   720500008

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
            Aplasia cutis congenita with intestinal lymphangiectasia syndrome   720500008

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
            Aplasia cutis congenita with intestinal lymphangiectasia syndrome   720500008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Aplasia cutis congenita with intestinal lymphangiectasia syndrome   720500008

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