Release 4B Snapshot #1

This page is part of the FHIR Specification (v4.3.0-snapshot1: Release 4B Snapshot #1). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions . Page versions: R4B R4 R3

Observation-example-genetics-2.xml

Orders and Observations Work GroupMaturity Level: N/AStandards Status: InformativeCompartments: Device, Encounter, Patient, Practitioner, RelatedPerson

Raw XML (canonical form + also see XML Format Specification)

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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"/> 
  <text> <status value="generated"/> <div xmlns="http://www.w3.org/1999/xhtml"><p> <b> Generated Narrative</b> </p> <div> <p> 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.
         <span>  (<a> LOINC</a> #55233-1)</span> </p> <p> <b> subject</b> : <a> Patient/example: Molecular Lab Patient ID: HOSP-23456</a>  &quot;Peter CHALMERS&quot;</p> <p> <b> issued</b> : 4 Apr. 2013, 1:30:10 am</p> <p> <b> performer</b> : <a> Practitioner/example: Molecular Diagnostics Laboratory</a>  &quot;Adam CAREFUL&quot;</p> <p> <b> value</b> : Positive <span>  (<a> SNOMED CT</a> #10828004)</span> </p> <p> <b> derivedFrom</b> : <a> Observation/example-genetics-1</a> </p> <blockquote> <p> <b> component</b> </p> <p> <b> code</b> : Genetic disease assessed <span>  (<a> LOINC</a> #51967-8)</span> </p> <p> <b> value</b> : Lung cancer <span>  (<a> 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>  (<a> LOINC</a> #53037-8)</span> </p> <p> <b> value</b> : Pathogenic <span>  ([not stated]#LA6669-1)</span> </p> </blockquote> </div> </text> <status value="final"/> 
  <code> 
    <coding> 
      <system value="http://loinc.org"/> 
      <code value="55233-1"/> 
      <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> 
  <issued 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> 
  <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> 

Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.