Hypertriglyceridemia SNOMED
Metadata
- Coding system
- SNOMED CT (UK Clinical Edition)
- Coding system release
- unknown
- Organisation
- University of Bristol
- Codelist ID
- bristol/hypertriglyceridemia-snomed
- Version ID
- 282e82e9
- Number of codes included
- 15
About
No metadata has been provided for this codelist.
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| 129591001 | Mixed hypercholesterolemia and hypertriglyceridemia |
| 238083002 | Primary hypertriglyceridemia |
| 238084008 | Very low density lipoprotinemia |
| 238085009 | Fredrickson type IV hyperlipoproteinemia |
| 238087001 | Secondary hypertriglyceridemia |
| 267433009 | Pure hyperglyceridemia |
| 267435002 | Familial hyperchylomicronemia |
| 302870006 | Hypertriglyceridemia |
| 33513003 | Familial apolipoprotein C-II deficiency |
| 34349009 | Familial type 5 hyperlipoproteinemia |
| 34528009 | Familial hypertriglyceridemia |
| 402473001 | Sporadic primary hypertriglyceridemia |
| 403827000 | Familial lipoprotein lipase deficiency with type I phenotype |
| 403828005 | Familial lipoprotein lipase deficiency with type V phenotype |
| 773649005 | Transient infantile hypertriglyceridemia and hepatosteatosis |
This page shows the search terms that were used to build the codelist. Concepts that match the search terms, but which were excluded, are in faint grey.
hypertriglyceridemia
Included 15 out of 17 matching concepts.
Show matching concepts
-
Familial apolipoprotein C-II deficiency (
33513003) -
Familial hyperchylomicronemia (
267435002) -
Familial hypertriglyceridemia (
34528009) -
Familial lipoprotein lipase deficiency (
275598004) -
Familial lipoprotein lipase deficiency with type I phenotype (
403827000) -
Familial lipoprotein lipase deficiency with type V phenotype (
403828005) -
Familial type 5 hyperlipoproteinemia (
34349009) -
Family history: Triglyceride high (
275939003) -
Fredrickson type IV hyperlipoproteinemia (
238085009) -
Hypertriglyceridemia (
302870006) -
Mixed hypercholesterolemia and hypertriglyceridemia (
129591001) -
Primary hypertriglyceridemia (
238083002) -
Pure hyperglyceridemia (
267433009) -
Secondary hypertriglyceridemia (
238087001) -
Sporadic primary hypertriglyceridemia (
402473001) -
Transient infantile hypertriglyceridemia and hepatosteatosis (
773649005) -
Very low density lipoprotinemia (
238084008)