FHIR Release 3 (STU) R4 Ballot #1 (Mixed Normative/Trial use)

This page is part of the FHIR Specification (v3.0.2: STU 3). (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'})

Relateds - Type

Target * derived-from 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.