Tryptophan malabsorption syndrome 59531002
SNOMED CT code
| SNOMED code | 59531002 |
|---|---|
| name | Tryptophan malabsorption syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Tryptophan malabsorption syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Structure of parenchyma of kidney 29704000 |
| Associated morphology | Pathologic calcification 18115005 |
| attributes - group2 | |
| Finding site | Gastrointestinal tract structure 122865005 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic renal disease 106000008 Nephrocalcinosis 48638002 Microscopic nephrocalcinosis 236444003 Tryptophan malabsorption syndrome 59531002 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Gastrointestinal tract finding 386618008 Disorder of gastrointestinal tract 119292006 Malabsorption syndrome 32230006 Tryptophan malabsorption syndrome 59531002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of organic acid metabolism 116021002 Disorder of amino acid metabolism 44779003 Disorder of amino acid and organic acid metabolism 237911005 Disorder of tryptophan metabolism 5181007 Tryptophan malabsorption syndrome 59531002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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