R4 Ballot #2 (Mixed Normative/Trial use)

This page is part of the FHIR Specification (v3.5.0: R4 Ballot #2). 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/ABallot 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 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--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> (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.'})</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', given as 'Positive'})</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> (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', 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' = '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--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.