Hirschsprung's disease   204739008

SNOMED CT code


SNOMED code204739008
nameHirschsprung's disease
statusactive
date introduced2002-01-31
fully specified name(s)Congenital aganglionic megacolon (disorder)
synonyms
  • Hirschsprung disease
  • Aganglionic megacolon
  • Congenital aganglionic megacolon
  • Aganglionosis
  • HD - Hirschsprung's disease
  • Hirschsprung's disease
attributes - group2
Pathological processPathological developmental process   308490002
Associated morphologyHypertrophy   56246009
OccurrenceCongenital   255399007
Finding siteLarge intestine part   119214008
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyDilatation   25322007
OccurrenceCongenital   255399007
Finding siteLarge intestine part   119214008
attributes - group3
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
Finding siteAutonomic nerve structure   53520000
OccurrenceCongenital   255399007
attributes - group4
Finding siteStructure of peripheral part of autonomic nervous system   429921001
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
parents
  • Congenital anomaly of the peripheral nervous system   22133005
  • Aganglionosis of large intestine   723183004
  • Motility disorder of large intestine   737198009
  • Congenital dilatation of intestinal tract   93058003
children
  • Aganglionosis of Auerbach's plexus   360434004
  • Extensive aganglionosis Hirschsprung disease   721609009
  • Goldberg Shprintzen megacolon syndrome   717822006
  • Haddad syndrome   719972004
  • Hirschsprung disease of rectosigmoid region   721608001
  • Hirschsprung disease with deafness and polydactyly syndrome   721221000
  • Hirschsprung disease with nail hypoplasia and dysmorphism   721223002
  • Hirschsprung disease with type D brachydactyly syndrome   721222007
  • Hirschsprung's disease NOS   204742002  removed: 2010-01-31
  • Long segment Hirschsprung's disease   204740005
  • Mowat-Wilson syndrome   703535000
  • Short segment Hirschsprung's disease   204741009
  • Total intestinal aganglionosis   204745000
  • Waardenburg Shah syndrome   715952000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of nervous system   118940003
          Disorder of the peripheral nervous system   42658009
            Congenital anomaly of the peripheral nervous system   22133005
              Hirschsprung's disease   204739008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of nervous system   118940003
          Disorder of autonomic nervous system   15241006
            Congenital malformation of autonomic nervous system   722996009
              Aganglionosis of large intestine   723183004
                Hirschsprung's disease   204739008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Viscus structure finding   406123005
      Abdominal organ finding   249561001
        Bowel finding   249562008
          Finding of large intestine   118436003
            Disorder of large intestine   119523007
              Motility disorder of large intestine   737198009
                Hirschsprung's disease   204739008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Gastrointestinal tract finding   386618008
        Disorder of gastrointestinal tract   119292006
          Dilatation of gastrointestinal tract   735499005
            Dilatation of intestine   86247009
              Congenital dilatation of intestinal tract   93058003
                Hirschsprung's disease   204739008

ancestors
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