minimal Common Oncology Data Elements (mCODE) Implementation Guide
2.1.0 - STU 2.1 United States of America flag

This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v2.1.0: STU 2) based on FHIR R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions

Example DiagnosticReport: genomics-report-john-anyperson

Master HL7 genetic variant reporting panel (Laboratory, Genetics)

SubjectJohn B. Anyperson male, DoB: 1951-01-20 ( Medical Record Number: m123 (use: USUAL))
When For2019-04-01
Reported2019-04-01 11:45:33+1100

Report Details

CodeValueFlagsWhen ForReported
Genetic variant assessmentPresentPositive (qualifier value)2019-04-01
DNA region of interest panel2019-04-01

Notes:

Instance: genomics-report-john-anyperson
InstanceOf: GenomicsReport
Title: "genomics-report-john-anyperson"
Description: "mCODE Example for Genomics Report"
Usage: #example
* status = #final
* category = http://terminology.hl7.org/CodeSystem/v2-0074#GE
* code = http://loinc.org#51969-4 "Genetic analysis report"
* subject = Reference(cancer-patient-john-anyperson)
* effectiveDateTime = "2019-04-01"
* issued = "2019-04-01T11:45:33+11:00"
* specimen = Reference(genomic-specimen-lung)
* result[0] = Reference(genomic-variant-somatic-single-nucleotide)
* result[+] = Reference(genomic-region-studied-stk11)