This page is part of the Genetic Reporting Implementation Guide (v3.0.0-ballot: STU 3 Ballot 1) based on FHIR (HL7® FHIR® Standard) R4. The current version which supersedes this version is 2.0.0. For a full list of available versions, see the Directory of published versions
<RiskAssessment xmlns="http://hl7.org/fhir">
<id value="GenRiskDiabetesT2"/>
<text>
<status value="generated"/>
<div xmlns="http://www.w3.org/1999/xhtml"><p><b>Generated Narrative: RiskAssessment</b><a name="GenRiskDiabetesT2"> </a></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 RiskAssessment "GenRiskDiabetesT2" </p></div><p><b>parent</b>: <a href="Observation-PolyGenicDiagnosticImpExample.html">Observation/PolyGenicDiagnosticImpExample</a></p><p><b>status</b>: final</p><p><b>subject</b>: <a href="Patient-CGPatientExample01.html">Patient/CGPatientExample01</a> " EVERYMAN"</p><p><b>basis</b>: </p><ul><li><span>: Variant 1</span></li><li><span>: Variant 2</span></li><li><span>: Variant 3</span></li><li><span>: Variant 4</span></li><li><span>: Variant 5</span></li><li><span>: Variant 6</span></li><li><span>: Variant 7</span></li></ul><blockquote><p><b>prediction</b></p><p><b>outcome</b>: Diabetes mellitus type 2 (disorder) <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://browser.ihtsdotools.org/">SNOMED CT</a>#44054006)</span></p><p><b>probability</b>: 0.26</p><p><b>qualitativeRisk</b>: Low likelihood <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="http://terminology.hl7.org/5.3.0/CodeSystem-risk-probability.html">Risk Probability</a>#low)</span></p><p><b>relativeRisk</b>: 1.05</p><p><b>when</b>: ?-53</p></blockquote><blockquote><p><b>prediction</b></p><p><b>outcome</b>: Diabetes mellitus type 2 (disorder) <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://browser.ihtsdotools.org/">SNOMED CT</a>#44054006)</span></p><p><b>probability</b>: 0.7</p><p><b>qualitativeRisk</b>: High likelihood <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="http://terminology.hl7.org/5.3.0/CodeSystem-risk-probability.html">Risk Probability</a>#high)</span></p><p><b>relativeRisk</b>: 2.69</p><p><b>when</b>: ?-65</p></blockquote></div>
</text>
<parent>🔗
<reference value="Observation/PolyGenicDiagnosticImpExample"/>
</parent>
<status value="final"/>
<subject>🔗
<reference value="Patient/CGPatientExample01"/>
</subject>
<basis>
<identifier>
<system value="http://hospital.example.org"/>
<value value="11"/>
</identifier>
<display value="Variant 1"/>
</basis>
<basis>
<identifier>
<system value="http://hospital.example.org"/>
<value value="12"/>
</identifier>
<display value="Variant 2"/>
</basis>
<basis>
<identifier>
<system value="http://hospital.example.org"/>
<value value="13"/>
</identifier>
<display value="Variant 3"/>
</basis>
<basis>
<identifier>
<system value="http://hospital.example.org"/>
<value value="14"/>
</identifier>
<display value="Variant 4"/>
</basis>
<basis>
<identifier>
<system value="http://hospital.example.org"/>
<value value="15"/>
</identifier>
<display value="Variant 5"/>
</basis>
<basis>
<identifier>
<system value="http://hospital.example.org"/>
<value value="16"/>
</identifier>
<display value="Variant 6"/>
</basis>
<basis>
<identifier>
<system value="http://hospital.example.org"/>
<value value="17"/>
</identifier>
<display value="Variant 7"/>
</basis>
<prediction>
<outcome>
<coding>
<system value="http://snomed.info/sct"/>
<code value="44054006"/>
<display value="Diabetes mellitus type 2 (disorder)"/>
</coding>
</outcome>
<probabilityDecimal value="0.26"/>
<qualitativeRisk>
<coding>
<system
value="http://terminology.hl7.org/CodeSystem/risk-probability"/>
<code value="low"/>
<display value="Low likelihood"/>
</coding>
</qualitativeRisk>
<relativeRisk value="1.05"/>
<whenRange>
<high>
<value value="53"/>
<unit value="years"/>
<system value="http://unitsofmeasure.org"/>
<code value="a"/>
</high>
</whenRange>
</prediction>
<prediction>
<outcome>
<coding>
<system value="http://snomed.info/sct"/>
<code value="44054006"/>
<display value="Diabetes mellitus type 2 (disorder)"/>
</coding>
</outcome>
<probabilityDecimal value="0.7"/>
<qualitativeRisk>
<coding>
<system
value="http://terminology.hl7.org/CodeSystem/risk-probability"/>
<code value="high"/>
<display value="High likelihood"/>
</coding>
</qualitativeRisk>
<relativeRisk value="2.69"/>
<whenRange>
<high>
<value value="65"/>
<unit value="years"/>
<system value="http://unitsofmeasure.org"/>
<code value="a"/>
</high>
</whenRange>
</prediction>
</RiskAssessment>
IG © 2022+ HL7 International / Clinical Genomics. Package hl7.fhir.uv.genomics-reporting#3.0.0-ballot based on FHIR 4.0.1. Generated 2023-12-18
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