Generated Narrative: ValueSet R5-genomicstudy-changetype-for-R3

This value set expansion contains 5 concepts.

SystemVersionCodeDisplayDefinition
http://hl7.org/fhir/genomicstudy-changetype5.0.0  AAProtein/amino Acids changeChange that involves Amino Acid (AA) or protein sequences.
http://hl7.org/fhir/genomicstudy-changetype5.0.0  CHRChromosomal changesChange that involves number or strcture of chromosomes.
http://hl7.org/fhir/genomicstudy-changetype5.0.0  CNVCopy number variationsChange that involves copy number variations among various genomes.
http://hl7.org/fhir/genomicstudy-changetype5.0.0  DNADNA changeChange that involves Deoxyribonucleic acid (DNA) sequences.
http://hl7.org/fhir/genomicstudy-changetype5.0.0  RNARNA changeChange that involves Ribonucleic Acid (RNA) sequences.
 <status value="active"/> <experimental value="false"/> <date value="2026-03-17T21:02:03.8104715+00:00"/> <publisher value="Clinical Genomics"/> <contact> <name value="Clinical Genomics"/> <telecom> <system value="url"/> <value value="http://www.hl7.org/Special/committees/clingenomics"/> </telecom> </contact> <description value="This cross-version ValueSet represents content from `http://hl7.org/fhir/ValueSet/genomicstudy-changetype|5.0.0` for use in FHIR STU3."/> <jurisdiction> <coding> <system value="http://unstats.un.org/unsd/methods/m49/m49.htm"/> <code value="001"/> <display value="World"/> </coding> </jurisdiction> <purpose value="This value set is part of the cross-version definitions generated to enable use of the value set `http://hl7.org/fhir/ValueSet/genomicstudy-changetype|5.0.0` as defined in FHIR R5 in FHIR STU3. The source value set is bound to the following FHIR R5 elements: * `GenomicStudy.analysis.changeType` Note that all concepts are included in this cross-version definition because no concepts have compatible representations Following are the generation technical comments: FHIR ValueSet `http://hl7.org/fhir/ValueSet/genomicstudy-changetype|5.0.0`, defined in FHIR R5 does not have any mapping to FHIR STU3"/> <compose> <include> <system value="http://hl7.org/fhir/genomicstudy-changetype"/> <version value="5.0.0"/> <concept> <code value="AA"/> <display value="Protein/amino Acids change"/> </concept> <concept> <code value="CHR"/> <display value="Chromosomal changes"/> </concept> <concept> <code value="CNV"/> <display value="Copy number variations"/> </concept> <concept> <code value="DNA"/> <display value="DNA change"/> </concept> <concept> <code value="RNA"/> <display value="RNA change"/> </concept> </include> </compose> <expansion> <timestamp value="2026-03-17T21:02:03.8104715+00:00"/> <contains> <system value="http://hl7.org/fhir/genomicstudy-changetype"/> <version value="5.0.0"/> <code value="AA"/> <display value="Protein/amino Acids change"/> </contains> <contains> <system value="http://hl7.org/fhir/genomicstudy-changetype"/> <version value="5.0.0"/> <code value="CHR"/> <display value="Chromosomal changes"/> </contains> <contains> <system value="http://hl7.org/fhir/genomicstudy-changetype"/> <version value="5.0.0"/> <code value="CNV"/> <display value="Copy number variations"/> </contains> <contains> <system value="http://hl7.org/fhir/genomicstudy-changetype"/> <version value="5.0.0"/> <code value="DNA"/> <display value="DNA change"/> </contains> <contains> <system value="http://hl7.org/fhir/genomicstudy-changetype"/> <version value="5.0.0"/> <code value="RNA"/> <display value="RNA change"/> </contains> </expansion> </ValueSet>