Intestinal enteropeptidase deficiency 56661000
SNOMED CT code
| SNOMED code | 56661000 |
|---|---|
| name | Intestinal enteropeptidase deficiency |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Intestinal enteropeptidase deficiency (disorder) |
| synonyms |
|
| attributes - group3 | |
| Due to | Deficiency of enteropeptidase 124498007 |
| attributes - group2 | |
| Finding site | Intestinal structure 113276009 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| parents | |
| 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 Gastrointestinal complication 24813008 Intestinal enteropeptidase deficiency 56661000 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Gastrointestinal tract finding 386618008 Disorder of gastrointestinal tract 119292006 Malabsorption syndrome 32230006 Intestinal enteropeptidase deficiency 56661000 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Intestinal enteropeptidase deficiency 56661000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Intestinal enteropeptidase deficiency 56661000 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Bowel finding 249562008 Disorder of intestine 85919009 Intestinal enteropeptidase deficiency 56661000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Intestinal enteropeptidase deficiency 56661000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Intestinal enteropeptidase deficiency 56661000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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