Clinical Genomics Resource Incubator, published by HL7 International / Clinical Genomics. This guide is not an authorized publication; it is the continuous build for version 0.1.0-ci-build built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/cg-incubator/ and changes regularly. See the Directory of published versions

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: Genomic Study Change Type

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<CodeSystem xmlns="http://hl7.org/fhir">
  <id value="genomicstudy-changetype"/>
  <meta>
    <lastUpdated value="2022-08-17T15:47:24.148-05:00"/>
    <profile
             value="http://hl7.org/fhir/StructureDefinition/shareablecodesystem"/>
  </meta>
  <language value="en"/>
  <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><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: 2022-08-17 15:47:24-0500</p><p style="margin-bottom: 0px">Profile: <a href="http://hl7.org/fhir/R5/shareablecodesystem.html">Shareable CodeSystem</a></p></div><p>This case-sensitive code system <code>http://hl7.org/fhir/uv/cg-incubator/CodeSystem/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="draft"/>
  </extension>
  <extension
             url="http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm">
    <valueInteger value="1"/>
  </extension>
  <url
       value="http://hl7.org/fhir/uv/cg-incubator/CodeSystem/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="0.1.0-ci-build"/>
  <name value="GenomicStudyChangeType"/>
  <title value="Genomic Study Change Type"/>
  <status value="draft"/>
  <experimental value="true"/>
  <date value="2022-08-17T15:48:24-05:00"/>
  <publisher value="HL7 International / Clinical Genomics"/>
  <contact>
    <name value="HL7 International / Clinical Genomics"/>
    <telecom>
      <system value="url"/>
      <value value="http://www.hl7.org/Special/committees/clingenomics"/>
    </telecom>
    <telecom>
      <system value="email"/>
      <value value="clingenomics@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/uv/cg-incubator/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>