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. For a full list of available versions, see the Directory of published versions
{
"resourceType" : "Observation",
"id" : "Pgx-geno-1001",
"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 Pgx-geno-1001</b></p><a name=\"Pgx-geno-1001\"> </a><a name=\"hcPgx-geno-1001\"> </a><a name=\"Pgx-geno-1001-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:{http://www.ncbi.nlm.nih.gov/clinvar 638797}\">CYP2C19*2/*2</span></p><p><b>specimen</b>: <a href=\"Specimen-GenomicSpecimenExample01.html\">Specimen: status = available; type = Tissue</a></p><p><b>derivedFrom</b>: </p><ul><li><a href=\"Observation-Pgx-var-1011.html\">Observation Genetic variant assessment</a></li><li><a href=\"Observation-Pgx-var-1012.html\">Observation Genetic variant assessment</a></li><li><a href=\"Observation-Pgx-var-1013.html\">Observation Genetic variant assessment</a></li><li><a href=\"Observation-Pgx-var-1014.html\">Observation Genetic variant assessment</a></li><li><a href=\"Observation-Pgx-var-1015.html\">Observation Genetic variant assessment</a></li><li><a href=\"Observation-Pgx-var-1016.html\">Observation Genetic variant assessment</a></li><li><a href=\"Observation-Pgx-var-1017.html\">Observation Genetic variant assessment</a></li><li><a href=\"Observation-Pgx-var-1018.html\">Observation Genetic variant assessment</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:2621}\">CYP2C19</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" : {
"coding" : [
{
"system" : "http://www.ncbi.nlm.nih.gov/clinvar",
"code" : "638797",
"display" : "CYP2C19*2/*2"
}
]
},
"specimen" : {
🔗 "reference" : "Specimen/GenomicSpecimenExample01"
},
"derivedFrom" : [
{
🔗 "reference" : "Observation/Pgx-var-1011"
},
{
🔗 "reference" : "Observation/Pgx-var-1012"
},
{
🔗 "reference" : "Observation/Pgx-var-1013"
},
{
🔗 "reference" : "Observation/Pgx-var-1014"
},
{
🔗 "reference" : "Observation/Pgx-var-1015"
},
{
🔗 "reference" : "Observation/Pgx-var-1016"
},
{
🔗 "reference" : "Observation/Pgx-var-1017"
},
{
🔗 "reference" : "Observation/Pgx-var-1018"
}
],
"component" : [
{
"code" : {
"coding" : [
{
"system" : "http://loinc.org",
"code" : "48018-6"
}
]
},
"valueCodeableConcept" : {
"coding" : [
{
"system" : "http://www.genenames.org",
"code" : "HGNC:2621",
"display" : "CYP2C19"
}
]
}
}
]
}