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
<Observation xmlns="http://hl7.org/fhir">
<id value="Pgx-geno-1001"/>
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<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 (use: usual, ))</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>
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<status value="final"/>
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<code value="laboratory"/>
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<category>
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<system value="http://terminology.hl7.org/CodeSystem/v2-0074"/>
<code value="GE"/>
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<code>
<coding>
<system value="http://loinc.org"/>
<code value="84413-4"/>
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<subject>🔗
<reference value="Patient/CGPatientExample01"/>
</subject>
<effectiveDateTime value="2019-04-01"/>
<performer>🔗
<reference value="Organization/ExampleOrg"/>
</performer>
<valueCodeableConcept>
<coding>
<system value="http://www.ncbi.nlm.nih.gov/clinvar"/>
<code value="638797"/>
<display value="CYP2C19*2/*2"/>
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<specimen>🔗
<reference value="Specimen/GenomicSpecimenExample01"/>
</specimen>
<derivedFrom>🔗
<reference value="Observation/Pgx-var-1011"/>
</derivedFrom>
<derivedFrom>🔗
<reference value="Observation/Pgx-var-1012"/>
</derivedFrom>
<derivedFrom>🔗
<reference value="Observation/Pgx-var-1013"/>
</derivedFrom>
<derivedFrom>🔗
<reference value="Observation/Pgx-var-1014"/>
</derivedFrom>
<derivedFrom>🔗
<reference value="Observation/Pgx-var-1015"/>
</derivedFrom>
<derivedFrom>🔗
<reference value="Observation/Pgx-var-1016"/>
</derivedFrom>
<derivedFrom>🔗
<reference value="Observation/Pgx-var-1017"/>
</derivedFrom>
<derivedFrom>🔗
<reference value="Observation/Pgx-var-1018"/>
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<system value="http://loinc.org"/>
<code value="48018-6"/>
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<coding>
<system value="http://www.genenames.org"/>
<code value="HGNC:2621"/>
<display value="CYP2C19"/>
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</Observation>