Release 4 4B

This page is part of the FHIR Specification (v4.0.1: R4 (v4.3.0: R4B - 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 R4B R4

Observation-example-genetics-brcapat

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. This example conforms to the profile Observation-genetics (FHIR Specification Core)).

Generated Narrative with Details

Resource "example-genetics-brcapat"

id Gene : example-genetics-brcapat BRCA (nuccore#KX470182.1)

status : final

code : BRCA1+BRCA2 gene mutations tested for The material on this page will be removed in Blood or Tissue by Molecular genetics method Nominal (Details : {LOINC code '59041-4' = 'BRCA1+BRCA2 gene mutations tested 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 in Blood or Tissue by Molecular genetics method Nominal', given as 'BRCA1+BRCA2 guidance. BRCA1+BRCA2 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal'}) 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.