Observation-example-genetics-2.xml

Genetics example 2 (id = "example-genetics-2")

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

<Observation xmlns="http://hl7.org/fhir">
  <id value="example-genetics-2"/> 
  : Genetic analysis master panel--This is the parent OBR for the panel holding all of the

  <text> <status value="generated"/> <div xmlns="http://www.w3.org/1999/xhtml"><p> <b> Generated Narrative</b> </p> <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">Resource &quot;example-genetics-2&quot; </p> </div> <p> <b> status</b> : final</p> <p> <b> code</b> : The material on this page will be removed in a future release. This content is deprecated
         and SHOULD NOT be used. Implementers are instead directed to the ([Genomics Reporting
         Implementation Guide](http://hl7.org/fhir/uv/genomics-reporting/index.html)) for guidance.
         Genetic analysis master panel--This is the parent OBR for the panel holding all of the

         associated observations that can be reported with a molecular genetics analysis result.
         (Details : {LOINC code '55233-1' = 'Genetic analysis master panel - Blood or Tissue by
           Molecular genetics method', given as 'Genetic analysis master panel--This is the parent
           OBR for the panel holding all of the associated observations that can be reported with
           a molecular genetics analysis result.'})(Details : {LOINC code '51967-8' = 'Genetic disease assessed [Identifier] in Blood or
             Tissue by Molecular genetics method', given as 'Genetic disease assessed'})(Details : {SNOMED CT code '363358000' = 'Malignant tumor of lung', given as 'Malignant
             tumor of lung (disorder)'})(Details : {LOINC code '53037-8' = 'Genetic disease sequence variation interpretation
             [interpretation] in Blood or Tissue by Molecular genetics method', given as 'Genetic disease
             sequence variation interpretation'})

         <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://loinc.org/">LOINC</a> #55233-1)</span> </p> <p> <b> subject</b> : <a href="patient-example.html">Patient/example: Molecular Lab Patient ID: HOSP-23456</a>  &quot;Peter CHALMERS&quot;</p> <p> <b> effective</b> : 2013-04-03T15:30:10+01:00</p> <p> <b> performer</b> : <a href="practitioner-example.html">Practitioner/example: Molecular Diagnostics Laboratory</a>  &quot;Adam CAREFUL&quot;</p> <p> <b> value</b> : Positive <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://browser.ihtsdotools.org/">SNOMED CT</a> #10828004)</span> </p> <p> <b> device</b> : <a href="device-example.html">Device/example</a> </p> <p> <b> derivedFrom</b> : <a href="observation-example-genetics-1.html">Observation/example-genetics-1</a> </p> <blockquote> <p> <b> component</b> </p> <p> <b> code</b> : Genetic disease assessed <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://loinc.org/">LOINC</a> #51967-8)</span> </p> <p> <b> value</b> : Lung cancer <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://browser.ihtsdotools.org/">SNOMED CT</a> #363358000 &quot;Malignant tumor of lung (disorder)&quot;)</span> </p> </blockquote> <blockquote> <p> <b> component</b> </p> <p> <b> code</b> : Genetic disease sequence variation interpretation <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://loinc.org/">LOINC</a> #53037-8)</span> </p> <p> <b> value</b> : Pathogenic <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> ([not stated]#LA6669-1)</span> </p> </blockquote> </div> </text> <status value="final"/> 
  <code> 
    <coding> 
      <system value="http://loinc.org"/> 
      <code value="55233-1"/> 
      Genetic analysis master panel--This is the parent OBR for the panel holding all of the

      <display value="The material on this page will be removed in a future release. This content is deprecated
       and SHOULD NOT be used. Implementers are instead directed to the ([Genomics Reporting
       Implementation Guide](http://hl7.org/fhir/uv/genomics-reporting/index.html)) for guidance.
       Genetic analysis master panel--This is the parent OBR for the panel holding all of the

       associated observations that can be reported with a molecular genetics analysis result."/> 
    </coding> 
  </code> 
  <subject> 
    
    

    <reference value="Patient/example"/> 
    <display value="Molecular Lab Patient ID: HOSP-23456"/> 
  </subject> 
  

  <effectiveDateTime value="2013-04-03T15:30:10+01:00"/> 
  <performer> 
    
    

    <reference value="Practitioner/example"/> 
    <display value="Molecular Diagnostics Laboratory"/> 
  </performer> 
  <valueCodeableConcept> 
    <coding> 
      <system value="http://snomed.info/sct"/> 
      <code value="10828004"/> 
      <display value="Positive"/> 
    </coding> 
  </valueCodeableConcept> 
  <device> 
    <reference value="Device/example"/> 
  </device>   
  <derivedFrom> 
    

    <reference value="Observation/example-genetics-1"/> 
  </derivedFrom> 
  <component> 
    <code> 
      <coding> 
        <system value="http://loinc.org"/> 
        <code value="51967-8"/> 
        <display value="Genetic disease assessed"/> 
      </coding> 
    </code> 
    <valueCodeableConcept> 
      <coding> 
        <system value="http://snomed.info/sct"/> 
        <code value="363358000"/> 
        <display value="Malignant tumor of lung (disorder)"/> 
      </coding> 
      <text value="Lung cancer"/> 
    </valueCodeableConcept> 
  </component> 
  <component> 
    <code> 
      <coding> 
        <system value="http://loinc.org"/> 
        <code value="53037-8"/> 
        <display value="Genetic disease sequence variation interpretation"/> 
      </coding> 
    </code> 
    <valueCodeableConcept> 
      <coding> 
        <code value="LA6669-1"/> 
        <display value="Pathogenic"/> 
      </coding> 
    </valueCodeableConcept> 
  </component> 


</

Observation

>