Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
resourceType | ValueSet |
id | 2.16.840.1.113762.1.4.1222.741 |
canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.741 |
version | 20210915 |
status | active |
publisher | HL7 Patient Care WG Steward |
name | Hypertriglyceridemia |
title | Hypertriglyceridemia |
date | 2021-09-15T01:01:30-04:00 |
experimental | false |
description | Documented diagnosis of Hypertriglyceridemia (Business ID: Entry 187476) |
Usages |
|
This value set contains 13 concepts
Code | System | Display |
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) |
267433009 | http://snomed.info/sct | Pure hyperglyceridemia (disorder) |
267435002 | http://snomed.info/sct | Familial hyperchylomicronemia (disorder) |
302870006 | http://snomed.info/sct | Hypertriglyceridemia (disorder) |
34349009 | http://snomed.info/sct | Familial type 5 hyperlipoproteinemia (disorder) |
34528009 | http://snomed.info/sct | Familial hypertriglyceridemia (disorder) |
402473001 | http://snomed.info/sct | Sporadic primary hypertriglyceridemia (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) |
773649005 | http://snomed.info/sct | Transient infantile hypertriglyceridemia and hepatosteatosis (disorder) |
Produced 08 Sep 2023