This page is part of the FHIR Specification (v4.0.1: R4 - Mixed Normative and STU) in it's permanent home (it will always be available at this URL). 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
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)
Example of breast cancer genetic observation (id = "example-genetics-brcapat")
<?xml version="1.0" encoding="UTF-8"?> <Observation xmlns="http://hl7.org/fhir"> <id value="example-genetics-brcapat"/> <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-brcapat</p> <p> <b> status</b> : final</p> <p> <b> code</b> : BRCA1+BRCA2 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal <span> (Details : {LOINC code '59041-4' = 'BRCA1+BRCA2 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal', given as 'BRCA1+BRCA2 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal'})</span> </p> <p> <b> subject</b> : <a> Patient1 with Breast Cancer FamilyHistory</a> </p> </div> </text> <extension url="http://hl7.org/fhir/StructureDefinition/observation-geneticsGene"> <valueCodeableConcept> <coding> <system value="https://www.ncbi.nlm.nih.gov/nuccore"/> <code value="KX470182.1"/> <display value="BRCA"/> </coding> </valueCodeableConcept> </extension> <extension url="http://hl7.org/fhir/us/core/StructureDefinition/us-core-ethnicity"> <valueCodeableConcept> <coding> <system value="http://browser.ihtsdotools.org/"/> <code value="413581001"/> <display value="Unknown racial group"/> </coding> </valueCodeableConcept> </extension> <status value="final"/> <code> <coding> <system value="http://loinc.org"/> <code value="59041-4"/> <display value="BRCA1+BRCA2 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal"/> </coding> </code> <subject> <reference value="Patient/brcapat"/> <display value="Patient1 with Breast Cancer FamilyHistory"/> </subject> </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.