OMOP Concept 4029260
Primary hypertriglyceridemia
StandardConditionSNOMED238083002Disorder
Maps from
2
Descendants
10
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Primary hypertriglyceridemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 129113 | Primary hypertriglyceridemia | Non-standard |
| Nebraska Lexicon | 238083002 | Primary hypertriglyceridaemia | Non-standard |
Synonyms
Alternative names recorded for Primary hypertriglyceridemia across source vocabularies.
- hipertrigliceridemia primaria
- hipertrigliceridemia primaria (trastorno)
- Primary hypertriglyceridaemia
- Primary hypertriglyceridemia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Hypertriglyceridemia
- 2Hyperlipidemia
- 3Disorder of lipoprotein storage and metabolism
- 3Lipid above reference range
- 4Disorder of lipoprotein AND/OR lipid metabolism
- 4Lipids outside reference range
- 4Measurement finding above reference range
- 5Lipid level - finding
- 5Measurement finding outside reference range
- 5Metabolic disease
- 6Disease
- 6Finding of substance level
- 6Measurement finding
- 7Clinical finding
- 7Evaluation finding
- 8Procedure related finding
Narrower concepts
(10)Included automatically when you query with descendants.
- 1Familial hypertriglyceridemia
- 1Sporadic primary hypertriglyceridemia
- 1Xanthoma due to primary hypertriglyceridemia
- 2Familial hyperchylomicronemia
- 2Familial type 5 hyperlipoproteinemia
- 2Fredrickson type IV hyperlipoproteinemia
- 2Transient infantile hypertriglyceridemia and hepatosteatosis
- 2Very low density lipoprotinemia
- 3Familial lipoprotein lipase deficiency with type I phenotype
- 3Familial lipoprotein lipase deficiency with type V phenotype
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