Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells   722392003

SNOMED CT code


SNOMED code722392003
nameCongenital malabsorptive diarrhea due to paucity of enteroendocrine cells
statusactive
date introduced2017-01-31
fully specified name(s)Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder)
synonyms
  • Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells
  • Congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells
  • Enteric anendocrinosis
attributes - group4
Clinical courseChronic   90734009
attributes - group3
OccurrenceCongenital   255399007
Finding siteGastrointestinal tract structure   122865005
attributes - group1
Finding siteIntestinal structure   113276009
parents
  • Chronic diarrhea of infants AND/OR young children   25319005
  • Malabsorption syndrome   32230006
  • Digestive system hereditary disorder   363080007
  • Congenital disease   66091009
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Diarrhea   62315008
        Chronic diarrhea   236071009
          Chronic diarrhea of infants AND/OR young children   25319005
            Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells   722392003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Gastrointestinal tract finding   386618008
        Disorder of gastrointestinal tract   119292006
          Malabsorption syndrome   32230006
            Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells   722392003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Disorder of digestive system   53619000
        Digestive system hereditary disorder   363080007
          Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells   722392003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells   722392003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells   722392003

ancestors
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