Pancreatic triacylglycerol lipase deficiency 78960005
SNOMED CT code
| SNOMED code | 78960005 |
|---|---|
| name | Pancreatic triacylglycerol lipase deficiency |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Pancreatic triacylglycerol lipase deficiency (disorder) |
| synonyms |
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| attributes - group3 | |
| Finding site | Gastrointestinal tract structure 122865005 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Finding site | Pancreatic structure 15776009 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Disorder of lysosomal enzyme 23585005 Pancreatic triacylglycerol lipase deficiency 78960005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of lipoprotein AND/OR lipid metabolism 48286001 Disorder of lipid storage and metabolism 238017009 Pancreatic triacylglycerol lipase deficiency 78960005 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Gastrointestinal tract finding 386618008 Disorder of gastrointestinal tract 119292006 Malabsorption syndrome 32230006 Pancreatic triacylglycerol lipase deficiency 78960005 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Pancreatic triacylglycerol lipase deficiency 78960005 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 triacylglycerol lipase deficiency 78960005 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Finding of pancreas 300357002 Disorder of pancreas 3855007 Pancreatic triacylglycerol lipase deficiency 78960005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Pancreatic triacylglycerol lipase deficiency 78960005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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