Definition for Code SystemGenomicStudyChangeType

<?xml version="1.0" encoding="UTF-8"?>

<CodeSystem xmlns="http://hl7.org/fhir">
  <id value="genomicstudy-changetype"/> 
  <meta> 
    <lastUpdated value="2022-09-06T19:58:29.429-05:00"/> 
    <profile value="http://hl7.org/fhir/StructureDefinition/shareablecodesystem"/> 
  </meta> 
  <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-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="0"/> 
  </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="5.0.0-ballot"/> 
  <name value="GenomicStudyChangeType"/> 
  <title value="GenomicStudyChangeType"/> 
  <status value="draft"/> 
  <experimental value="false"/> 
  <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."/> 
  <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>