OMOP Concept 4031945
Primary hypercholesterolemia
StandardConditionSNOMED238076009Disorder
Maps from
2
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
2 source codes normalize to Primary hypercholesterolemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 129117 | Primary hypercholesterolaemia | Non-standard |
| Nebraska Lexicon | 238076009 | Primary hypercholesterolaemia | Non-standard |
Synonyms
Alternative names recorded for Primary hypercholesterolemia across source vocabularies.
- hipercolesterolemia primaria
- hipercolesterolemia primaria (trastorno)
- Primary hypercholesterolaemia
- Primary hypercholesterolemia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(29)Roll up to these when you need a wider cohort.
- 1Hypercholesterolemia
- 2Hyperlipidemia
- 2Serum cholesterol above reference range
- 3Disorder of lipoprotein storage and metabolism
- 3Lipid above reference range
- 3Serum cholesterol outside reference range
- 3Serum lipids above reference range
- 4Blood substance level above reference range
- 4Disorder of lipoprotein AND/OR lipid metabolism
- 4Lipids outside reference range
- 4Measurement finding above reference range
- 4Serum cholesterol level - finding
- 4Serum lipid levels - finding
- 5Cholesterol level - finding
- 5Finding of blood substance level
- 5Lipid level - finding
- 5Measurement finding outside reference range
- 5Metabolic disease
- 6Disease
- 6Finding of substance level
- 6Measurement finding
- 7Clinical finding
- 7Evaluation finding
- 7Measurement of substance
- 8Measurement
Narrower concepts
(13)Included automatically when you query with descendants.
- 1Familial defective apolipoprotein B-100
- 1Familial hypercholesterolemia
- 1Hyperalphalipoproteinemia
- 1Polygenic hypercholesterolemia
- 1Xanthoma due to primary hypercholesterolemia
- 2Double heterozygous familial hypercholesterolemia
- 2Familial hyperalphalipoproteinemia
- 2Familial hypercholesterolemia due to genetic defect of apolipoprotein B
- 2Familial hypercholesterolemia due to heterozygous LDL receptor mutation
- 2Familial hypercholesterolemia due to homozygous LDL receptor mutation
- 2Familial hypercholesterolemia - heterozygous
- 2Familial hypercholesterolemia - homozygous
- 2Fredrickson type IIa hyperlipoproteinemia
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