OMOP Concept 4120314
Hypertriglyceridemia
StandardConditionSNOMED302870006Disorder
Maps from
8
Descendants
13
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
8 source codes normalize to Hypertriglyceridemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 117374 | Predisposition to Hypertriglyceridemia | Non-standard |
| CIEL | 117375 | High Blood Triglycerides | Non-standard |
| CIEL | 117377 | Hyperglyceridemia | Non-standard |
| HPO | HP_0002155 | Hypertriglyceridemia | Non-standard |
| MeSH | D015228 | Hypertriglyceridemia | Non-standard |
| Nebraska Lexicon | 302870006 | Hypertriglyceridaemia | Non-standard |
| OXMIS | 2720TG | HYPERTRIGLYCERIDAEMIA | Non-standard |
| Read | C321000 | Hypertriglyceridaemia | Non-standard |
Synonyms
Alternative names recorded for Hypertriglyceridemia across source vocabularies.
- hipertrigliceridemia
- hipertrigliceridemia (trastorno)
- Hypertriglyceridaemia
- Hypertriglyceridemia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
- 1Hyperlipidemia
- 2Disorder of lipoprotein storage and metabolism
- 2Lipid above reference range
- 3Disorder of lipoprotein AND/OR lipid metabolism
- 3Lipids outside reference range
- 3Measurement finding above reference range
- 4Lipid level - finding
- 4Measurement finding outside reference range
- 4Metabolic disease
- 5Disease
- 5Finding of substance level
- 5Measurement finding
- 6Clinical finding
- 6Evaluation finding
- 7Procedure related finding
Narrower concepts
(13)Included automatically when you query with descendants.
- 1Primary hypertriglyceridemia
- 1Pure hyperglyceridemia
- 1Secondary hypertriglyceridemia
- 2Familial hypertriglyceridemia
- 2Sporadic primary hypertriglyceridemia
- 2Xanthoma due to primary hypertriglyceridemia
- 3Familial hyperchylomicronemia
- 3Familial type 5 hyperlipoproteinemia
- 3Fredrickson type IV hyperlipoproteinemia
- 3Transient infantile hypertriglyceridemia and hepatosteatosis
- 3Very low density lipoprotinemia
- 4Familial lipoprotein lipase deficiency with type I phenotype
- 4Familial lipoprotein lipase deficiency with type V phenotype
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