This page is part of the Genetic Reporting Implementation Guide (v3.0.0: STU3) based on FHIR (HL7® FHIR® Standard) 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" : "Observation",
"id" : "Genotype-Clinical-Trial-Example-using-haplotypes",
"meta" : {
"profile" : [
🔗 "http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genotype"
]
},
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: Observation Genotype-Clinical-Trial-Example-using-haplotypes</b></p><a name=\"Genotype-Clinical-Trial-Example-using-haplotypes\"> </a><a name=\"hcGenotype-Clinical-Trial-Example-using-haplotypes\"> </a><a name=\"Genotype-Clinical-Trial-Example-using-haplotypes-en-US\"> </a><p><b>status</b>: Final</p><p><b>category</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/observation-category laboratory}\">Laboratory</span>, <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/v2-0074 GE}\">Genetics</span></p><p><b>code</b>: <span title=\"Codes:{http://loinc.org 84413-4}\">Genotype display name</span></p><p><b>subject</b>: <a href=\"Patient-CGPatientExample01.html\">Adam B. Everyman Male, DoB: 1951-01-20 ( Medical Record Number: m123\u00a0(use:\u00a0usual,\u00a0))</a></p><p><b>effective</b>: 2019-04-01</p><p><b>performer</b>: <a href=\"Organization-ExampleOrg.html\">Organization some lab</a></p><p><b>value</b>: <span title=\"Codes:\">APOE e1/e1</span></p><p><b>specimen</b>: <a href=\"Specimen-GenomicSpecimenExample02.html\">Specimen: identifier = http://myorgsurl.com#123; accessionIdentifier = http://mylabsurl.com#456; status = available; type = Buccal smear sample</a></p><p><b>derivedFrom</b>: </p><ul><li><a href=\"Observation-HaplotypeSet-Clinical-Trial-Example-1of2.html\">Observation Haplotype name</a></li><li><a href=\"Observation-HaplotypeSet-Clinical-Trial-Example-2of2.html\">Observation Haplotype name</a></li></ul><h3>Components</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Code</b></td><td><b>Value[x]</b></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{http://loinc.org 48018-6}\">Gene studied [ID]</span></td><td><span title=\"Codes:{http://www.genenames.org HGNC:613}\">APOE</span></td></tr></table></div>"
},
"status" : "final",
"category" : [
{
"coding" : [
{
"system" : "http://terminology.hl7.org/CodeSystem/observation-category",
"code" : "laboratory"
}
]
},
{
"coding" : [
{
"system" : "http://terminology.hl7.org/CodeSystem/v2-0074",
"code" : "GE"
}
]
}
],
"code" : {
"coding" : [
{
"system" : "http://loinc.org",
"code" : "84413-4"
}
]
},
"subject" : {
🔗 "reference" : "Patient/CGPatientExample01"
},
"effectiveDateTime" : "2019-04-01",
"performer" : [
{
🔗 "reference" : "Organization/ExampleOrg"
}
],
"valueCodeableConcept" : {
"text" : "APOE e1/e1"
},
"specimen" : {
🔗 "reference" : "Specimen/GenomicSpecimenExample02"
},
"derivedFrom" : [
{
🔗 "reference" : "Observation/HaplotypeSet-Clinical-Trial-Example-1of2"
},
{
🔗 "reference" : "Observation/HaplotypeSet-Clinical-Trial-Example-2of2"
}
],
"component" : [
{
"code" : {
"coding" : [
{
"system" : "http://loinc.org",
"code" : "48018-6"
}
]
},
"valueCodeableConcept" : {
"coding" : [
{
"system" : "http://www.genenames.org",
"code" : "HGNC:613",
"display" : "APOE"
}
]
}
}
]
}