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
Orders and Observations Work Group | Maturity Level: N/A | Standards Status: Informative | Compartments: Device, Encounter, Patient, Practitioner, RelatedPerson |
Raw XML (canonical form + also see XML Format Specification)
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 "example-genetics-2" </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> "Peter CHALMERS"</p> <p> <b> issued</b> : 4 Apr. 2013, 1:30:10 am</p> <p> <b> performer</b> : <a> Practitioner/example: Molecular Diagnostics Laboratory</a> "Adam CAREFUL"</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 "Malignant tumor of lung (disorder)")</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.