This page is part of the Genetic Reporting Implementation Guide (v2.0.0: STU 2) based on FHIR R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions
{
"resourceType" : "ServiceRequest",
"id" : "eMERGEServiceRequest",
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative</b></p><div style=\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"><p style=\"margin-bottom: 0px\">Resource \"eMERGEServiceRequest\" </p></div><p><b>status</b>: completed</p><p><b>intent</b>: order</p><p><b>code</b>: emerge-seq-ngs-pnl <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (#emerge-seq-ngs-pnl)</span></p><p><b>subject</b>: <a href=\"Patient-CGPatientExample01.html\">Patient/CGPatientExample01</a> \" EVERYMAN\"</p><p><b>specimen</b>: <a href=\"Specimen-GenomicSpecimenExample01.html\">Specimen/GenomicSpecimenExample01</a></p></div>"
},
"status" : "completed",
"intent" : "order",
"code" : {
"coding" : [
{
"system" : "https://hgsc.bcm.edu/lab-test-codes/",
"code" : "emerge-seq-ngs-pnl"
}
]
},
"subject" : {
"reference" : "Patient/CGPatientExample01"
},
"specimen" : [
{
"reference" : "Specimen/GenomicSpecimenExample01"
}
]
}