This is the Continuous Integration Build of FHIR (will be incorrect/inconsistent at times).
See the Directory of published versions icon CodeSystem http://hl7.org/fhir/genomicstudy-changetype

Clinical Genomics icon Work Group Maturity Level: 1Trial Use Use Context: Country: World, Not yet ready for Production use
Official URL: http://hl7.org/fhir/genomicstudy-changetype Version: 6.0.0-cibuild
active as of 2022-08-17 Computable Name: GenomicStudyChangeType
Flags: Experimental, CaseSensitive, Complete. All codes ValueSet: Genomic Study Change Type OID: 2.16.840.1.113883.4.642.4.1977

This Code system is used in the following value sets:

The change type relevant to GenomicStudy analysis.

This case-sensitive code system http://hl7.org/fhir/genomicstudy-changetype defines the following codes:

DNA DNA changeChange that involves Deoxyribonucleic acid (DNA) sequences.btn btn
RNA RNA changeChange that involves Ribonucleic Acid (RNA) sequences.btn btn
AA Protein/amino Acids change Change that involves Amino Acid (AA) or protein sequences.btn btn
CHR Chromosomal changesChange that involves number or strcture of chromosomes.btn btn
CNV Copy number variationsChange that involves copy number variations among various genomes.btn btn


See the full registry of code systems defined as part of FHIR.

Explanation of the columns that may appear on this page:

LevelA few code lists that FHIR defines are hierarchical - each code is assigned a level. See Code System for further information.
SourceThe source of the definition of the code (when the value set draws in codes defined elsewhere)
CodeThe code (used as the code in the resource instance). If the code is in italics, this indicates that the code is not selectable ('Abstract')
DisplayThe display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
DefinitionAn explanation of the meaning of the concept
CommentsAdditional notes about how to use the code