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 |
This is the narrative for the resource. See also the XML, JSON or Turtle format.
Generated Narrative
Resource "example-genetics-brcapat"
Gene: BRCA (nuccore#KX470182.1)
status: final
code: 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 (LOINC#59041-4)
subject: Patient/brcapat: Patient1 with Breast Cancer FamilyHistory
effective: 2021-03-03T14:50:23-05:00
device: Device/example
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.