This page is part of the FHIR Specification (v1.0.0: DSTU 2 Ballot 3). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions
This is the narrative for the resource. See also the XML or JSON format. This example conforms to the profile Standard Profile for Genetics (FHIR Specification Core)).
Generated Narrative with Details
id: genetics-example3-mutationlist-3
status: final
code: ABCB4 gene mutation analysis (Details : {LOINC code '49874-1' = 'ABCB4 gene mutation analysis in Blood or Tissue by Molecular genetics method Narrative', given as 'ABCB4 gene mutation analysis'})
subject: Molecular Lab Patient ID: HOSP-23456
performer: Molecular Diagnostic Laboratory
specimen: Molecular Specimen ID: MLD45-Z4-1234
- | Code | Value[x] |
* | Genetic disease sequence variation interpretation (Details : {LOINC code '53037-8' = 'Genetic disease sequence variation interpretation [interpretation] in Blood or Tissue by Molecular genetics method', given as 'Genetic disease sequence variation interpretation'}) | Benign (Details : {http://www.genenames.org code 'LA6675-8' = '??', given as 'Benign'}) |
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.