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Clinical Genomics Work Group | Maturity Level: N/A | Standards Status: Informative |
Raw XML (canonical form + also see XML Format Specification)
Definition for Code SystemGenomicStudyChangeType
<?xml version="1.0" encoding="UTF-8"?> <CodeSystem xmlns="http://hl7.org/fhir"> <id value="genomicstudy-changetype"/> <meta> <lastUpdated value="2024-10-02T12:31:51.554-05:00"/> <profile value="http://hl7.org/fhir/StructureDefinition/shareablecodesystem"/> </meta> <text> <status value="generated"/> <div xmlns="http://www.w3.org/1999/xhtml"> <p class="res-header-id"> <b> Generated Narrative: CodeSystem genomicstudy-changetype</b> </p> <a name="genomicstudy-changetype"> </a> <a name="hcgenomicstudy-changetype"> </a> <a name="genomicstudy-changetype-en-US"> </a> <div style="display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%"> <p style="margin-bottom: 0px">Last updated: 2022-08-17T15:47:24.148-05:00</p> <p style="margin-bottom: 0px">Profile: <a href="shareablecodesystem.html">Shareable CodeSystem</a> </p> </div> <p> This case-sensitive code system <code> http://hl7.org/fhir/genomicstudy-changetype</code> defines the following codes: </p> <table class="codes"> <tr> <td style="white-space:nowrap"> <b> Code</b> </td> <td> <b> Display</b> </td> <td> <b> Definition</b> </td> </tr> <tr> <td style="white-space:nowrap">DNA <a name="genomicstudy-changetype-DNA"> </a> </td> <td> DNA change</td> <td> Change that involves Deoxyribonucleic acid (DNA) sequences.</td> </tr> <tr> <td style="white-space:nowrap">RNA <a name="genomicstudy-changetype-RNA"> </a> </td> <td> RNA change</td> <td> Change that involves Ribonucleic Acid (RNA) sequences.</td> </tr> <tr> <td style="white-space:nowrap">AA <a name="genomicstudy-changetype-AA"> </a> </td> <td> Protein/amino Acids change </td> <td> Change that involves Amino Acid (AA) or protein sequences.</td> </tr> <tr> <td style="white-space:nowrap">CHR <a name="genomicstudy-changetype-CHR"> </a> </td> <td> Chromosomal changes</td> <td> Change that involves number or strcture of chromosomes.</td> </tr> <tr> <td style="white-space:nowrap">CNV <a name="genomicstudy-changetype-CNV"> </a> </td> <td> Copy number variations</td> <td> Change that involves copy number variations among various genomes.</td> </tr> </table> </div> </text> <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-wg"> <valueCode value="cg"/> </extension> <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status"> <valueCode value="trial-use"/> </extension> <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm"> <valueInteger value="1"/> </extension> <url value="http://hl7.org/fhir/genomicstudy-changetype"/> <identifier> <system value="urn:ietf:rfc:3986"/> <value value="urn:oid:2.16.840.1.113883.4.642.4.1977"/> </identifier> <version value="6.0.0-ballot2"/> <name value="GenomicStudyChangeType"/> <title value="Genomic Study Change Type"/> <status value="active"/> <experimental value="true"/> <date value="2022-08-17T15:48:24-05:00"/> <publisher value="HL7 (FHIR Project)"/> <contact> <telecom> <system value="url"/> <value value="http://hl7.org/fhir"/> </telecom> <telecom> <system value="email"/> <value value="fhir@lists.hl7.org"/> </telecom> </contact> <description value="The change type relevant to GenomicStudy analysis."/> <jurisdiction> <coding> <system value="http://unstats.un.org/unsd/methods/m49/m49.htm"/> <code value="001"/> <display value="World"/> </coding> </jurisdiction> <caseSensitive value="true"/> <valueSet value="http://hl7.org/fhir/ValueSet/genomicstudy-changetype"/> <content value="complete"/> <concept> <code value="DNA"/> <display value="DNA change"/> <definition value="Change that involves Deoxyribonucleic acid (DNA) sequences."/> </concept> <concept> <code value="RNA"/> <display value="RNA change"/> <definition value="Change that involves Ribonucleic Acid (RNA) sequences."/> </concept> <concept> <code value="AA"/> <display value="Protein/amino Acids change "/> <definition value="Change that involves Amino Acid (AA) or protein sequences."/> </concept> <concept> <code value="CHR"/> <display value="Chromosomal changes"/> <definition value="Change that involves number or strcture of chromosomes."/> </concept> <concept> <code value="CNV"/> <display value="Copy number variations"/> <definition value="Change that involves copy number variations among various genomes."/> </concept> </CodeSystem>
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.
FHIR ®© HL7.org 2011+. FHIR R6 hl7.fhir.core#6.0.0-ballot2 generated on Wed, Oct 2, 2024 17:55+0000.
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