ValueSet-2.16.840.1.113762.1.4.1032.15

Sourceus.nlm.vsac#0.11.0:null (v4.0.1)
resourceTypeValueSet
id2.16.840.1.113762.1.4.1032.15
canonicalhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1032.15
version20170526
statusactive
publisherMITRE Steward
nameFamilialHypercholesterolemia
titleFamilial Hypercholesterolemia
date2022-03-18T01:03:56-04:00
experimentalfalse
Usages(none)

This value set contains 14 concepts

Code System Display
   238040008 http://snomed.info/sct Familial combined hyperlipidemia (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)
   397915002 http://snomed.info/sct Fredrickson type IIa hyperlipoproteinemia (disorder)
   398036000 http://snomed.info/sct Familial hypercholesterolemia (disorder)
   398796005 http://snomed.info/sct Familial type 3 hyperlipoproteinemia (disorder)
   402474007 http://snomed.info/sct Primary polygenic type IIb combined hyperlipidemia (disorder)
   402787000 http://snomed.info/sct Primary genetic mixed hyperlipidemia (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)
   E78.01 http://hl7.org/fhir/sid/icd-10-cm Familial hypercholesterolemia

Produced 08 Sep 2023