This page is part of the FHIR Specification (v1.8.0: STU 3 Draft). 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
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--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 (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' = '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> <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.