Familial lipoprotein lipase deficiency with type I phenotype 403827000
SNOMED CT code
| SNOMED code | 403827000 |
|---|---|
| name | Familial lipoprotein lipase deficiency with type I phenotype |
| status | active |
| date introduced | 2003-07-31 |
| fully specified name(s) | Familial lipoprotein lipase deficiency with type I phenotype (disorder) |
| synonyms |
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| attributes - group1 | |
| Interprets | Lipids measurement 104780002 |
| Has interpretation | Above reference range 281302008 |
| parents | Familial hyperchylomicronemia 267435002 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of lipoprotein AND/OR lipid metabolism 48286001 Disorder of lipoprotein storage and metabolism 238037008 Hyperlipidemia 55822004 Hypertriglyceridemia 302870006 Primary hypertriglyceridemia 238083002 Familial hypertriglyceridemia 34528009 Familial hyperchylomicronemia 267435002 Familial lipoprotein lipase deficiency with type I phenotype 403827000 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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