OMOP Concept 4267672
Serum lipid levels - finding
StandardMeasurementSNOMED365798004Clinical Finding
Maps from
1
Descendants
35
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
1 source code normalizes to Serum lipid levels - finding via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 365798004 | Finding of serum lipid levels | Non-standard |
Synonyms
Alternative names recorded for Serum lipid levels - finding across source vocabularies.
- Finding of serum lipid levels
- Finding of serum lipid levels (finding)
- niveles de lípido sérico - hallazgo
- niveles de lípido sérico - hallazgo (hallazgo)
- Serum lipid levels
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(7)Roll up to these when you need a wider cohort.
Narrower concepts
(35)Included automatically when you query with descendants.
- 1Serum cholesterol level - finding
- 1Serum lipids above reference range
- 1Serum lipids within reference range
- 1Serum sodium valproate level - finding
- 1Serum triglyceride levels - finding
- 2Serum cholesterol above reference range
- 2Serum cholesterol outside reference range
- 2Serum cholesterol within reference range
- 2Serum sodium valproate above therapeutic range
- 2Serum sodium valproate below therapeutic range
- 2Serum sodium valproate within therapeutic range
- 2Serum triglycerides above reference range
- 2Serum triglycerides within reference range
- 3Hypercholesterolemia
- 3Serum cholesterol decreased
- 4Exacerbation of hypercholesterolemia
- 4Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency
- 4Hyperlipidemia, group A
- 4Primary hypercholesterolemia
- 4Pure hypercholesterolemia
- 4Secondary hypercholesterolemia
- 4TMEM199 congenital disorder of glycosylation
- 5Familial defective apolipoprotein B-100
- 5Familial hypercholesterolemia
- 5Hyperalphalipoproteinemia
- 5Polygenic hypercholesterolemia
- 5Xanthoma due to primary hypercholesterolemia
- 6Double heterozygous familial hypercholesterolemia
- 6Familial hyperalphalipoproteinemia
- 6Familial hypercholesterolemia due to genetic defect of apolipoprotein B
- 6Familial hypercholesterolemia due to heterozygous LDL receptor mutation
- 6Familial hypercholesterolemia due to homozygous LDL receptor mutation
- 6Familial hypercholesterolemia - heterozygous
- 6Familial hypercholesterolemia - homozygous
- 6Fredrickson type IIa hyperlipoproteinemia
Get this concept via the API
Resolve Serum lipid levels - finding - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/4267672?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card