Congenital microvillous atrophy   235729009

SNOMED CT code


SNOMED code235729009
nameCongenital microvillous atrophy
statusactive
date introduced2002-01-31
fully specified name(s)Congenital microvillous atrophy (disorder)
synonyms
  • Congenital microvillous atrophy
  • Davidson disease
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Associated morphologyMicrovillus alteration   125471000
Finding siteSmall intestinal structure   30315005
parents
  • Malabsorption syndrome   32230006
  • Congenital anomaly of small intestine   55193002
childrenFamilial absence of villi   235730004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Gastrointestinal tract finding   386618008
        Disorder of gastrointestinal tract   119292006
          Malabsorption syndrome   32230006
            Congenital microvillous atrophy   235729009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Viscus structure finding   406123005
      Abdominal organ finding   249561001
        Bowel finding   249562008
          Finding of small intestine   118435004
            Disorder of small intestine   119522002
              Congenital anomaly of small intestine   55193002
                Congenital microvillous atrophy   235729009

ancestors
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