This page is part of the FHIR Specification (v5.0.0: R5 - STU). This is the current published version in it's permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions
Clinical Genomics Work Group | Maturity Level: N/A | Standards Status: Informative | Compartments: Patient |
This is the narrative for the resource. See also the XML, JSON or Turtle format. This example conforms to the profile GenomicStudy.
Generated Narrative
Resource "genomicServiceRequest"
identifier: Laboratory Accession ID: 111111111
status: active
intent: plan
code: Carrier detection, molecular genetics (procedure) (SNOMED CT#3981005)
subject: Patient/denovoChild " DOE"
encounter: Encounter/denovoEncounter
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.