FHIR Cross-Version Extensions package for FHIR R4 from FHIR R5 - Version 0.0.1-snapshot-2. See the Directory of published versions

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: Genomic Study Change Type - XML Representation

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<CodeSystem xmlns="http://hl7.org/fhir">
  <id value="genomicstudy-changetype"/>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml">
            <p>This 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-standards-status">
    <valueCode value="informative"/>
  </extension>
  <extension
             url="http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm">
    <valueInteger value="1"/>
  </extension>
  <extension url="http://hl7.org/fhir/StructureDefinition/package-source">
    <extension url="packageId">
      <valueId value="hl7.fhir.uv.xver-r5.r4"/>
    </extension>
    <extension url="version">
      <valueString value="0.0.1-snapshot-2"/>
    </extension>
  </extension>
  <extension
             url="http://hl7.org/fhir/StructureDefinition/structuredefinition-wg">
    <valueCode value="cg"/>
  </extension>
  <url value="http://hl7.org/fhir/genomicstudy-changetype"/>
  <version value="5.0.0"/>
  <name value="GenomicStudyChangeType"/>
  <title value="Genomic Study Change Type"/>
  <status value="active"/>
  <experimental value="true"/>
  <date value="2022-08-18T06:48:24+10:00"/>
  <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="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>