This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v1.0.0: STU 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
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{ "resourceType" : "Observation", "id" : "mCODECancerGeneticVariantExample02", "meta" : { "profile" : [ "http://hl7.org/fhir/us/mcode/StructureDefinition/mcode-cancer-genetic-variant" ] }, "text" : { "status" : "generated", "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative with Details</b></p><p><b>id</b>: mCODECancerGeneticVariantExample02</p><p><b>meta</b>: </p><p><b>status</b>: final</p><p><b>category</b>: Laboratory <span style=\"background: LightGoldenRodYellow\">(Details : {http://terminology.hl7.org/CodeSystem/observation-category code 'laboratory' = 'Laboratory)</span></p><p><b>code</b>: Genetic variant assessment <span style=\"background: LightGoldenRodYellow\">(Details : {LOINC code '69548-6' = 'Genetic variant assessment)</span></p><p><b>subject</b>: <a href=\"Observation-mCODECancerGeneticVariantExample02.html\">Generated Summary: id: mCODEPatientExample01; Medical record number = m123 (USUAL); John B. Anyperson ; gender: male; birthDate: 1951-01-20</a></p><p><b>effective</b>: Apr 1, 2019 12:00:00 AM</p><p><b>value</b>: Present <span style=\"background: LightGoldenRodYellow\">(Details : {LOINC code 'LA9633-4' = 'Present)</span></p><p><b>method</b>: Sequencing <span style=\"background: LightGoldenRodYellow\">(Details : {LOINC code 'LA26398-0' = 'Sequencing)</span></p><blockquote><p><b>component</b></p><p><b>code</b>: Gene studied [ID] <span style=\"background: LightGoldenRodYellow\">(Details : {LOINC code '48018-6' = 'Gene studied [ID])</span></p><p><b>value</b>: HGNC:1100 <span style=\"background: LightGoldenRodYellow\">(Details : {http://www.genenames.org/geneId code 'HGNC:1100' = 'HGNC:1100)</span></p></blockquote><blockquote><p><b>component</b></p><p><b>code</b>: Genomic DNA change (gHGVS) <span style=\"background: LightGoldenRodYellow\">(Details : {LOINC code '81290-9' = 'Genomic DNA change (gHGVS))</span></p><p><b>value</b>: NG_005905.2:g.126148_126152GTAAA[1] <span style=\"background: LightGoldenRodYellow\">(Details : {http://varnomen.hgvs.org code 'NG_005905.2:g.126148_126152GTAAA[1]' = 'NG_005905.2:g.126148_126152GTAAA[1])</span></p></blockquote><blockquote><p><b>component</b></p><p><b>code</b>: Genomic source class [Type] <span style=\"background: LightGoldenRodYellow\">(Details : {LOINC code '48002-0' = 'Genomic source class [Type])</span></p><p><b>value</b>: Germline <span style=\"background: LightGoldenRodYellow\">(Details : {LOINC code 'LA6683-2' = 'Germline)</span></p></blockquote></div>" }, "status" : "final", "category" : [ { "coding" : [ { "system" : "http://terminology.hl7.org/CodeSystem/observation-category", "code" : "laboratory" } ] } ], "code" : { "coding" : [ { "system" : "http://loinc.org", "code" : "69548-6" } ] }, "subject" : { "reference" : "Patient/mCODEPatientExample01" }, "effectiveDateTime" : "2019-04-01", "valueCodeableConcept" : { "coding" : [ { "system" : "http://loinc.org", "code" : "LA9633-4" } ] }, "method" : { "coding" : [ { "system" : "http://loinc.org", "code" : "LA26398-0" } ] }, "component" : [ { "code" : { "coding" : [ { "system" : "http://loinc.org", "code" : "48018-6" } ] }, "valueCodeableConcept" : { "coding" : [ { "system" : "http://www.genenames.org/geneId", "code" : "HGNC:1100" } ] } }, { "code" : { "coding" : [ { "system" : "http://loinc.org", "code" : "81290-9" } ] }, "valueCodeableConcept" : { "coding" : [ { "system" : "http://varnomen.hgvs.org", "code" : "NG_005905.2:g.126148_126152GTAAA[1]" } ] } }, { "code" : { "coding" : [ { "system" : "http://loinc.org", "code" : "48002-0" } ] }, "valueCodeableConcept" : { "coding" : [ { "system" : "http://loinc.org", "code" : "LA6683-2" } ] } } ] }