| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113762.1.4.1222.75 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.75 |
| version | 20200407 |
| status | active |
| publisher | HL7 Patient Care WG Steward |
| name | HyperlipidemiaConditionsSCT |
| title | Hyperlipidemia Conditions SCT |
| date | 2020-04-07T01:02:08-04:00 |
| experimental | false |
| Usages |
|
This value set contains 59 concepts
| Code | System | Display |
| 114831000119107 | http://snomed.info/sct | Hyperlipidemia caused by steroid (disorder) |
| 1197489003 | http://snomed.info/sct | Familial chylomicronemia syndrome (disorder) |
| 1208738002 | http://snomed.info/sct | Transmembrane protein 199 congenital disorder of glycosylation (disorder) |
| 129589009 | http://snomed.info/sct | Endogenous hyperlipidemia (disorder) |
| 129590000 | http://snomed.info/sct | Exogenous hyperlipidemia (disorder) |
| 129591001 | http://snomed.info/sct | Mixed hypercholesterolemia and hypertriglyceridemia (disorder) |
| 13644009 | http://snomed.info/sct | Hypercholesterolemia (disorder) |
| 137931000119102 | http://snomed.info/sct | Hyperlipidemia due to type 2 diabetes mellitus (disorder) |
| 137941000119106 | http://snomed.info/sct | Hyperlipidemia due to type 1 diabetes mellitus (disorder) |
| 1571000119104 | http://snomed.info/sct | Mixed hyperlipidemia due to type 1 diabetes mellitus (disorder) |
| 15771000119109 | http://snomed.info/sct | Familial hyperalphalipoproteinemia (disorder) |
| 190774002 | http://snomed.info/sct | Hyperlipidemia, group A (disorder) |
| 238040008 | http://snomed.info/sct | Familial combined hyperlipidemia (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) |
| 238083002 | http://snomed.info/sct | Primary hypertriglyceridemia (disorder) |
| 238084008 | http://snomed.info/sct | Very low density lipoprotinemia (disorder) |
| 238085009 | http://snomed.info/sct | Fredrickson type IV hyperlipoproteinemia (disorder) |
| 238087001 | http://snomed.info/sct | Secondary hypertriglyceridemia (disorder) |
| 238088006 | http://snomed.info/sct | Primary combined hyperlipidemia (disorder) |
| 238089003 | http://snomed.info/sct | Secondary combined hyperlipidemia (disorder) |
| 267432004 | http://snomed.info/sct | Pure hypercholesterolemia (disorder) |
| 267433009 | http://snomed.info/sct | Pure hyperglyceridemia (disorder) |
| 267434003 | http://snomed.info/sct | Mixed hyperlipidemia (disorder) |
| 267435002 | http://snomed.info/sct | Familial hyperchylomicronemia (disorder) |
| 275598004 | http://snomed.info/sct | Familial lipoprotein lipase deficiency (disorder) |
| 299465007 | http://snomed.info/sct | Familial multiple lipoprotein-type hyperlipidemia (disorder) |
| 302870006 | http://snomed.info/sct | Hypertriglyceridemia (disorder) |
| 33513003 | http://snomed.info/sct | Familial apolipoprotein C-II deficiency (disorder) |
| 34349009 | http://snomed.info/sct | Familial type 5 hyperlipoproteinemia (disorder) |
| 34528009 | http://snomed.info/sct | Familial hypertriglyceridemia (disorder) |
| 397915002 | http://snomed.info/sct | Fredrickson type IIa hyperlipoproteinemia (disorder) |
| 398036000 | http://snomed.info/sct | Familial hypercholesterolemia (disorder) |
| 402473001 | http://snomed.info/sct | Sporadic primary hypertriglyceridemia (disorder) |
| 402474007 | http://snomed.info/sct | Primary polygenic type IIb combined hyperlipidemia (disorder) |
| 402475008 | http://snomed.info/sct | Primary acquired chylomicronemia (disorder) |
| 402725005 | http://snomed.info/sct | Hyperlipidemia with lipid deposition in skin (disorder) |
| 402726006 | http://snomed.info/sct | Primary chylomicronemia (disorder) |
| 402727002 | http://snomed.info/sct | Secondary hyperlipidemia (disorder) |
| 402785008 | http://snomed.info/sct | Primary genetic hyperlipidemia (disorder) |
| 402786009 | http://snomed.info/sct | Chylomicronemia syndrome (disorder) |
| 402787000 | http://snomed.info/sct | Primary genetic mixed hyperlipidemia (disorder) |
| 403827000 | http://snomed.info/sct | Familial lipoprotein lipase deficiency with type I phenotype (disorder) |
| 403828005 | http://snomed.info/sct | Familial lipoprotein lipase deficiency with type V phenotype (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) |
| 426161002 | http://snomed.info/sct | Chemically induced hyperlipidemia (disorder) |
| 445261005 | http://snomed.info/sct | Posttransplant hyperlipidemia (disorder) |
| 55822004 | http://snomed.info/sct | Hyperlipidemia (disorder) |
| 701000119103 | http://snomed.info/sct | Mixed hyperlipidemia due to type 2 diabetes mellitus (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) |
| 773649005 | http://snomed.info/sct | Transient infantile hypertriglyceridemia and hepatosteatosis (disorder) |
| 773726000 | http://snomed.info/sct | Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency (disorder) |
Produced 08 Sep 2023