R4 Ballot #1 (Mixed Normative/Trial use)

This page is part of the FHIR Specification (v3.3.0: R4 Ballot 2). 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 R3

Observation-example-genetics-2

Orders and Observations Work Group

Maturity Level: N/A

Ballot Status: Informative

Compartments: Device, Encounter, Patient, Practitioner, RelatedPerson

This is the narrative for the resource. See also the XML or JSON format. This example conforms to the profile Observation-genetics (FHIR Specification Core)).

Generated Narrative with Details

id: example-genetics-2

status: final

code: Genetic analysis master panel--This is the parent OBR for the panel holding all of the associated observations that can be reported with a molecular genetics analysis result. (Details : {LOINC code '55233-1' = 'Genetic analysis master panel - Blood or Tissue by Molecular genetics method', given as 'Genetic analysis master panel--This is the parent OBR for the panel holding all of the associated observations that can be reported with a molecular genetics analysis result.'})

subject: Molecular Lab Patient ID: HOSP-23456

issued: 03/04/2013 3:30:10 PM

performer: Molecular Diagnostics Laboratory

value: Positive (Details : {SNOMED CT code '10828004' = 'Positive', given as 'Positive'})

derivedFrom: Observation/example-genetics-1

component
code: Genetic disease assessed (Details : {LOINC code '51967-8' = 'Genetic disease assessed [Identifier] in Blood or Tissue by Molecular genetics method', given as 'Genetic disease assessed'})
value: Lung cancer (Details : {SNOMED CT code '363358000' = 'Malignant tumor of lung', given as 'Malignant tumor of lung (disorder)'})

component
code: 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'})
value: Pathogenic (Details : {[not stated] code 'LA6669-1' = 'LA6669-1', given as 'Pathogenic'})

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.