STU 3 Ballot

This page is part of the FHIR Specification (v1.6.0: STU 3 Ballot 4). 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

Raw XML (canonical form)

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

<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 with Details</b></p><p><b>id</b>: example-genetics-2</p><p><b>status</b>: final</p><p><b>code</b>: Genetic analysis master panel <span>(Details : {LOINC code '55233-1' = 'Genetic analysis master panel - Blood or Tissue by
           Molecular genetics method', given as 'Genetic analysis master panel'})</span></p><p><b>subject</b>: <a>Molecular Lab Patient ID: HOSP-23456</a></p><p><b>issued</b>: 03/04/2013 3:30:10 PM</p><p><b>performer</b>: <a>Molecular Diagnostics Laboratory</a></p><p><b>value</b>: Positive <span>(Details : {SNOMED CT code '10828004' = 'Positive (qualifier value)', given as 'Positive'})</span></p><h3>Relateds</h3><table><tr><td>-</td><td><b>Type</b></td><td><b>Target</b></td></tr><tr><td>*</td><td>derived-from</td><td><a>Observation/example-genetics-1</a></td></tr></table><blockquote><p><b>component</b></p><p><b>code</b>: Genetic disease assessed <span>(Details : {LOINC code '51967-8' = 'Genetic disease assessed [Identifier] in Blood or
             Tissue by Molecular genetics method', given as 'Genetic disease assessed'})</span></p><p><b>value</b>: Lung cancer <span>(Details : {SNOMED CT code '363358000' = 'Malignant tumor of lung (disorder)', given as
             'Malignant tumor of lung (disorder)'})</span></p></blockquote><blockquote><p><b>component</b></p><p><b>code</b>: Genetic disease sequence variation interpretation <span>(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></p><p><b>value</b>: Pathogenic <span>(Details : {[not stated] code 'LA6669-1' = '??', given as 'Pathogenic'})</span></p></blockquote></div></text><status value="final"/>
  <code>
    <coding>
      <system value="http://loinc.org"/>
      <code value="55233-1"/>
      <display value="Genetic analysis master panel"/>
    </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>
  <related>
    <type value="derived-from"/>
    <target>
      <reference value="Observation/example-genetics-1"/>
    </target>
  </related>
  <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.