This page is part of the FHIR Specification (v4.3.0: R4B - STU). 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="extensions"/> <div xmlns="http://www.w3.org/1999/xhtml"><p> <b> Generated Narrative</b> </p> <div style="display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%"><p style="margin-bottom: 0px">Resource "example-genetics-brcapat" </p> </div> <p> <b> Gene</b> : BRCA <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (nuccore#KX470182.1)</span> </p> <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. BRCA1+BRCA2 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://loinc.org/">LOINC</a> #59041-4)</span> </p> <p> <b> subject</b> : <a href="todo.html">Patient/brcapat: Patient1 with Breast Cancer FamilyHistory</a> </p> <p> <b> effective</b> : 2021-03-03T14:50:23-05:00</p> <p> <b> device</b> : <a href="device-example.html">Device/example</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="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. 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> <effectiveDateTime value="2021-03-03T14:50:23-05:00"/> <device> <reference value="Device/example"/> </device> </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.