Familial and non-familial hypercholesterolemia diagnosis codes
Codelist metadata
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Coding system
- SNOMED CT
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Coding system release
- unknown
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Organisation
- NHSD Primary Care Domain Refsets
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Codelist ID
- nhsd-primary-care-domain-refsets/fnfhyp_cod
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Version Tag
- 20200812
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Version ID
- 5757b3a4
Versions
About
Description
Taken from the FNFHYP_COD refset published by NHSD.
References
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 |
|---|---|
| 190773008 | Hyperbetalipoproteinemia |
| 190774002 | Hyperlipidemia, group A |
| 238038003 | Familial hyperlipoproteinemia |
| 238040008 | Familial combined hyperlipidemia |
| 238076009 | Primary hypercholesterolemia |
| 238077000 | Polygenic hypercholesterolemia |
| 238078005 | Familial hypercholesterolemia - homozygous |
| 238079002 | Familial hypercholesterolemia - heterozygous |
| 238081000 | Familial defective apolipoprotein B-100 |
| 238083002 | Primary hypertriglyceridemia |
| 238086005 | Fredrickson type I hyperlipoproteinemia |
| 238088006 | Primary combined hyperlipidemia |
| 267432004 | Pure hypercholesterolemia |
| 267434003 | Mixed hyperlipidemia |
| 267435002 | Familial hyperchylomicronemia |
| 299465007 | Familial multiple lipoprotein-type hyperlipidemia |
| 33513003 | Familial apolipoprotein C-II deficiency |
| 34349009 | Familial type 5 hyperlipoproteinemia |
| 34528009 | Familial hypertriglyceridemia |
| 397915002 | Fredrickson type IIa hyperlipoproteinemia |
| 398036000 | Familial hypercholesterolemia |
| 398796005 | Familial type 3 hyperlipoproteinemia |
| 403829002 | Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation |
| 403830007 | Familial hypercholesterolemia due to homozygous low density lipoprotein receptor mutation |
| 403831006 | Familial hypercholesterolemia due to genetic defect of apolipoprotein B |
| 445010006 | Low density lipoprotein receptor mutation |
| 57218003 | Cholesterol ester storage disease |
| 767133009 | Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations |
Codes not in the full codelist are in faint grey.