minimal Common Oncology Data Elements (mCODE) Implementation Guide
3.0.0-ballot - 2023May 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 (v3.0.0-ballot: STU 3 Ballot 1) based on FHIR R4. The current version which supercedes this version is 2.1.0. For a full list of available versions, see the Directory of published versions

Example DiagnosticReport: gx-genomics-report-adam-anyperson

Genetic analysis report (Genetics)

SubjectAdam Anyperson male, DoB: 1990-01-01 ( Medical Record Number: 123456789)
When For2022-02-15 19:28:58+0500

Report Details

CodeValueWhen For
Genetic variant assessmentPresent
Genetic variant assessmentPresent2019-04-01
Genetic variant assessmentPresent2019-04-01
Genetic variant assessmentPresent2019-04-01
Genetic variant assessmentPresent2019-04-01
Genetic variant assessmentPresent2019-04-01
Genetic variant assessmentPresent2019-04-01
Genetic variant assessmentPresent2019-04-01
Diagnostic Implication2019-04-01
Diagnostic Implication2019-04-01
Diagnostic Implication2019-04-01
Genetic variant assessmentPresent2019-04-01
Genetic variant assessmentAbsent2019-04-01
Mutations/Megabase [# Ratio] in Tumor57.1 1/1000000{Base}
Microsatellite instability [Interpretation] in Cancer specimen QualitativeMSI-H
Therapeutic Implication
Therapeutic Implication
Therapeutic Implication
Therapeutic Implication
Therapeutic Implication