Congenital monosaccharide malabsorption 450849003
SNOMED CT code
| SNOMED code | 450849003 |
|---|---|
| name | Congenital monosaccharide malabsorption |
| status | active |
| date introduced | 2012-07-31 |
| fully specified name(s) | Congenital monosaccharide malabsorption (disorder) |
| synonyms | Congenital monosaccharide malabsorption |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Finding site | Gastrointestinal tract structure 122865005 |
| parents | |
| children | Congenital glucose-galactose malabsorption 27943000 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of carbohydrate metabolism 20957000 Disorder of carbohydrate absorption 237972006 Congenital monosaccharide malabsorption 450849003 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Gastrointestinal tract finding 386618008 Disorder of gastrointestinal tract 119292006 Malabsorption syndrome 32230006 Congenital monosaccharide malabsorption 450849003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital monosaccharide malabsorption 450849003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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