ValueSet-2.16.840.1.113762.1.4.1196.1139

Sourceus.nlm.vsac#0.11.0:null (v4.0.1)
resourceTypeValueSet
id2.16.840.1.113762.1.4.1196.1139
canonicalhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1196.1139
version20220826
statusactive
publisherElimu Informatics Steward
nameS4GHyperlipidemia
titleS4G Hyperlipidemia
date2022-08-26T01:03:06-04:00
experimentalfalse
description(This is a sync for genes test value set. This is only a test value set.)
Usages(none)

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