Congenital microvillous atrophy 235729009
SNOMED CT code
SNOMED code | 235729009 |
---|---|
name | Congenital microvillous atrophy |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Congenital microvillous atrophy (disorder) |
synonyms |
|
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Microvillus alteration 125471000 |
Finding site | Small intestinal structure 30315005 |
parents | |
children | Familial absence of villi 235730004 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical 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 | sorted most to least specific
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cpt crosswalks |
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