This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v0.9.1: STU 1 Ballot 1) based on FHIR R4. The current version which supercedes this version is 2.0.0. For a full list of available versions, see the Directory of published versions
{ "resourceType" : "DiagnosticReport", "id" : "mCODEGenomicsReportExample01", "meta" : { "versionId" : "0.1", "lastUpdated" : "2019-04-01T15:35:58.045+00:00", "profile" : [ "http://hl7.org/fhir/us/mcode/StructureDefinition/onco-core-GenomicsReport" ] }, "text" : { "status" : "generated", "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>*** mCODE Example: Genomics Report ***</b></p><p><b>Test id</b>: mCODEGenomicsReportExample01</p><p><b>Performer</b>: Foundation Medicine</p><p><b>Test Name</b>: FoundationOne</p><p><b>Status</b>: final</p><p><b>Subject</b>: John B. Anyperson</p><p></p><p><b>Generated Summary:</b></p><p><b>id:</b> Medical Record Number = m123 (USUAL)</p><p><b>Effective</b>: 04/01/2019</p><p><b>Genetic Mutation Tested</b>: STK11</p><p><b>Gene variant presence</b>: DETECTED</p><p><b>Genomic source class</b>: Somatic</p><p><b>Variant HGVS name</b>: NM_000455.4:c.921-1G>C</p><p><b>Variant common name</b>: G242E</p></div>" }, "status" : "final", "category" : [ { "coding" : [ { "system" : "http://terminology.hl7.org/CodeSystem/v2-0074", "code" : "GE", "display" : "Genetics" } ] } ], "code" : { "coding" : [ { "system" : "http://www.ncbi.nlm.nih.gov/gtr", "code" : "GTR000527976.2", "display" : "FoundationOne" } ] }, "subject" : { "reference" : "Patient/mCODEPatientExample01", "display" : "John B. Anyperson" }, "effectiveDateTime" : "2019-04-01", "issued" : "2019-04-01T11:45:33+11:00", "performer" : [ { "reference" : "Organization/mCODEOrganizationExampleFM1" } ], "result" : [ { "reference" : "Observation/mCODEGeneticVariantTestedExample01" }, { "reference" : "Observation/mCODEGeneticVariantFoundExample01" } ] }