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
Generated Narrative: Observation
Resource Observation "gx-genomic-diagnostic-implication-polrmt"
Profile: Diagnostic Implication
status: final
category: Laboratory (Observation Category Codes#laboratory)
code: Diagnostic Implication (To Be Determined Codes#diagnostic-implication)
subject: Patient/gx-cancer-patient-adam-anyperson " ANYPERSON"
effective: 2019-04-01
derivedFrom: Observation/gx-genomic-variant-somatic-polrmt
- | Code | Value[x] |
* | Genetic variation clinical significance [Imp] (LOINC#53037-8) | Uncertain significance (LOINC#LA26333-7) |