This page is part of the Genetic Reporting Implementation Guide (v3.0.0-ballot: STU 3 Ballot 1) based on FHIR (HL7® FHIR® Standard) R4. The current version which supersedes this version is 2.0.0. For a full list of available versions, see the Directory of published versions
Generated Narrative: Observation
Resource Observation "ROS1-Fusion-disease"
Profile: Diagnostic Implication
status: final
category: Laboratory (Observation Category Codes#laboratory), Genetics (diagnosticServiceSectionId#GE)
code: Diagnostic Implication (To Be Determined Codes#diagnostic-implication)
subject: Patient/somaticPatient " HAMSBURG"
effective: 2023-02-01
performer: Practitioner/pathologistPractitioner " DOLIN"
derivedFrom: Observation/ROS1-Fusion-var
Code | Value[x] |
Genetic variation clinical significance [Imp] (LOINC#53037-8) | Pathogenic (LOINC#LA6668-3) |