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. For a full list of available versions, see the Directory of published versions
<Observation xmlns="http://hl7.org/fhir">
<id value="Therapeutic-Implication-Clinical-Trial-Somatic"/>
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<profile
value="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/therapeutic-implication"/>
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<text>
<status value="generated"/>
<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 "Therapeutic-Implication-Clinical-Trial-Somatic" </p><p style="margin-bottom: 0px">Profile: <a href="StructureDefinition-therapeutic-implication.html">Therapeutic Implication</a></p></div><p><b>status</b>: final</p><p><b>category</b>: Laboratory <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="http://terminology.hl7.org/3.1.0/CodeSystem-observation-category.html">Observation Category Codes</a>#laboratory)</span></p><p><b>code</b>: Therapeutic Implication <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="CodeSystem-tbd-codes-cs.html">To Be Determined Codes</a>#therapeutic-implication)</span></p><p><b>derivedFrom</b>: <a href="Observation-Variant-Somatic-Clinical-Trial.html">Observation/Variant-Somatic-Clinical-Trial</a></p><blockquote><p><b>component</b></p><p><b>code</b>: Predicted Therapeutic Implication <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="CodeSystem-tbd-codes-cs.html">To Be Determined Codes</a>#predicted-therapeutic-implication)</span></p><p><b>value</b>: Patient eligible for clinical trial <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://browser.ihtsdotools.org/">SNOMED CT</a>#399223003)</span></p></blockquote><blockquote><p><b>component</b></p><p><b>code</b>: Associated phenotype <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://loinc.org/">LOINC</a>#81259-4)</span></p><p><b>value</b>: Breast Cancer <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://browser.ihtsdotools.org/">SNOMED CT</a>#254837009)</span></p></blockquote><blockquote><p><b>component</b></p><p><b>code</b>: Associated Therapy <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="CodeSystem-tbd-codes-cs.html">To Be Determined Codes</a>#associated-therapy)</span></p><p><b>value</b>: NCT01234567 <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (#NCT01234567)</span></p></blockquote></div>
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<status value="final"/>
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<system value="http://terminology.hl7.org/CodeSystem/observation-category"/>
<code value="laboratory"/>
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<coding>
<system
value="http://hl7.org/fhir/uv/genomics-reporting/CodeSystem/tbd-codes-cs"/>
<code value="therapeutic-implication"/>
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<derivedFrom>
<reference value="Observation/Variant-Somatic-Clinical-Trial"/>
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<code>
<coding>
<system
value="http://hl7.org/fhir/uv/genomics-reporting/CodeSystem/tbd-codes-cs"/>
<code value="predicted-therapeutic-implication"/>
<display value="Predicted Therapeutic Implication"/>
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<coding>
<system value="http://snomed.info/sct"/>
<code value="399223003"/>
<display value="Patient eligible for clinical trial"/>
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<coding>
<system value="http://loinc.org"/>
<code value="81259-4"/>
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<coding>
<system value="http://snomed.info/sct"/>
<code value="254837009"/>
<display value="Breast Cancer"/>
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<component>
<code>
<coding>
<system
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<code value="associated-therapy"/>
<display value="Associated Therapy"/>
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<valueCodeableConcept>
<coding>
<system value="http://clinicaltrials.gov/"/>
<code value="NCT01234567"/>
<display value="NCT01234567"/>
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