Pancreatic colipase deficiency 69478001
SNOMED CT code
| SNOMED code | 69478001 |
|---|---|
| name | Pancreatic colipase deficiency |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Pancreatic colipase deficiency (disorder) |
| synonyms | Pancreatic colipase deficiency |
| attributes - group2 | |
| Finding site | Pancreatic structure 15776009 |
| attributes - group1 | |
| Finding site | Small intestinal structure 30315005 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Digestive system finding 386617003 Finding of pancreas 300357002 Disorder of pancreas 3855007 Pancreatic malabsorption 302920007 Pancreatic colipase deficiency 69478001 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Pancreatic colipase deficiency 69478001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Pancreatic colipase deficiency 69478001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Pancreatic colipase deficiency 69478001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Pancreatic colipase deficiency 69478001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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