| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113762.1.4.1078.428 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1078.428 |
| version | 20230324 |
| status | active |
| publisher | Optum Steward |
| name | HypercholesterolemiaSCT |
| title | Hypercholesterolemia SCT |
| date | 2023-03-24T01:02:43-04:00 |
| Usages |
|
This value set contains 20 concepts
| Code | System | Display |
| 1208738002 | http://snomed.info/sct | Transmembrane protein 199 congenital disorder of glycosylation (disorder) |
| 13644009 | http://snomed.info/sct | Hypercholesterolemia (disorder) |
| 15771000119109 | http://snomed.info/sct | Familial hyperalphalipoproteinemia (disorder) |
| 166830008 | http://snomed.info/sct | Serum cholesterol above reference range (finding) |
| 190774002 | http://snomed.info/sct | Hyperlipidemia, group A (disorder) |
| 238076009 | http://snomed.info/sct | Primary hypercholesterolemia (disorder) |
| 238077000 | http://snomed.info/sct | Polygenic hypercholesterolemia (disorder) |
| 238078005 | http://snomed.info/sct | Familial hypercholesterolemia - homozygous (disorder) |
| 238079002 | http://snomed.info/sct | Familial hypercholesterolemia - heterozygous (disorder) |
| 238080004 | http://snomed.info/sct | Hyperalphalipoproteinemia (disorder) |
| 238081000 | http://snomed.info/sct | Familial defective apolipoprotein B-100 (disorder) |
| 238082007 | http://snomed.info/sct | Secondary hypercholesterolemia (disorder) |
| 267432004 | http://snomed.info/sct | Pure hypercholesterolemia (disorder) |
| 397915002 | http://snomed.info/sct | Fredrickson type IIa hyperlipoproteinemia (disorder) |
| 398036000 | http://snomed.info/sct | Familial hypercholesterolemia (disorder) |
| 403829002 | http://snomed.info/sct | Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation (disorder) |
| 403830007 | http://snomed.info/sct | Familial hypercholesterolemia due to homozygous low density lipoprotein receptor mutation (disorder) |
| 403831006 | http://snomed.info/sct | Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder) |
| 767133009 | http://snomed.info/sct | Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations (disorder) |
| 773726000 | http://snomed.info/sct | Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency (disorder) |
Produced 08 Sep 2023