Valueset-LOINC-53037-8-answerlist.xml

Definition for Value SetLOINC 53037-8 answerlist

<ValueSet xmlns="http://hl7.org/fhir">
  <id value="LOINC-53037-8-answerlist"/>
  <meta>
    <lastUpdated value="2015-12-11T17:38:40.294+11:00"/>
    <profile value="http://hl7.org/fhir/StructureDefinition/valueset-shareable-definition"/>
  </meta>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml">
      <h2>LOINC 53037-8 answerlist</h2>
      <p>LOINC answer list for Genetic disease sequence variation interpretation</p>
      <p>This value set has an inline code system http://hl7.org/fhir/LOINC-53037-8-answerlist,
         which defines the following codes:</p>
      <table class="codes">
        <tr>
          <td>
            <b>Code</b>
          </td>
          <td>
            <b>Display</b>
          </td>
          <td>
            <b>Definition</b>
          </td>
        </tr>
        <tr>
          <td>LA6668-3
            <a name="LA6668-3"> </a>
          </td>
          <td>Pathogenic</td>
          <td>Pathogenic</td>
        </tr>
        <tr>
          <td>LA6669-1
            <a name="LA6669-1"> </a>
          </td>
          <td>Presumed pathogenic</td>
          <td>Presumed pathogenic</td>
        </tr>
        <tr>
          <td>LA6682-4
            <a name="LA6682-4"> </a>
          </td>
          <td>Unknown significance</td>
          <td>Unknown significance</td>
        </tr>
        <tr>
          <td>LA6675-8
            <a name="LA6675-8"> </a>
          </td>
          <td>Benign</td>
          <td>Benign</td>
        </tr>
        <tr>
          <td>LA6674-1
            <a name="LA6674-1"> </a>
          </td>
          <td>Presumed benign</td>
          <td>Presumed benign</td>
        </tr>
      </table>
    </div>
  </text>
  <extension url="http://hl7.org/fhir/StructureDefinition/valueset-oid">
    <valueUri value="urn:oid:2.16.840.1.113883.4.642.2.0"/>
  </extension>
  <url value="http://hl7.org/fhir/ValueSet/LOINC-53037-8-answerlist"/>
  <version value="1.2.0"/>
  <name value="LOINC 53037-8 answerlist"/>
  <status value="draft"/>
  <experimental value="false"/>
  <publisher value="HL7 (FHIR Project)"/>
  <contact>
    <telecom>
      <system value="other"/>
      <value value="http://hl7.org/fhir"/>
    </telecom>
    <telecom>
      <system value="email"/>
      <value value="fhir@lists.hl7.org"/>
    </telecom>
  </contact>
  <date value="2015-12-11T17:38:40+11:00"/>
  <description value="LOINC answer list for Genetic disease sequence variation interpretation"/>
  <codeSystem>
    <extension url="http://hl7.org/fhir/StructureDefinition/valueset-oid">
      <valueUri value="urn:oid:2.16.840.1.113883.4.642.1.0"/>
    </extension>
    <system value="http://hl7.org/fhir/LOINC-53037-8-answerlist"/>
    <version value="1.2.0"/>
    <caseSensitive value="true"/>
    <concept>
      <code value="LA6668-3"/>
      <display value="Pathogenic"/>
      <definition value="Pathogenic"/>
    </concept>
    <concept>
      <code value="LA6669-1"/>
      <display value="Presumed pathogenic"/>
      <definition value="Presumed pathogenic"/>
    </concept>
    <concept>
      <code value="LA6682-4"/>
      <display value="Unknown significance"/>
      <definition value="Unknown significance"/>
    </concept>
    <concept>
      <code value="LA6675-8"/>
      <display value="Benign"/>
      <definition value="Benign"/>
    </concept>
    <concept>
      <code value="LA6674-1"/>
      <display value="Presumed benign"/>
      <definition value="Presumed benign"/>
    </concept>
  </codeSystem>
</ValueSet>