0.2.0 - ci-build
GO_FHIR - Local Development build (v0.2.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions
| Active as of 2024-12-11 |
<CodeSystem xmlns="http://hl7.org/fhir">
<id value="variant-significance-codesystem"/>
<text>
<status value="generated"/>
<div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: CodeSystem variant-significance-codesystem</b></p><a name="variant-significance-codesystem"> </a><a name="hcvariant-significance-codesystem"> </a><a name="variant-significance-codesystem-en-US"> </a><p>This code system <code>http://fhir.genomoncology.io/CodeSystem/variant-significance-codesystem</code> defines the following codes:</p><table class="codes"><tr><td style="white-space:nowrap"><b>Code</b></td><td><b>Display</b></td></tr><tr><td style="white-space:nowrap">oncogenic<a name="variant-significance-codesystem-oncogenic"> </a></td><td>Oncogenic</td></tr><tr><td style="white-space:nowrap">likely_oncogenic<a name="variant-significance-codesystem-likely_oncogenic"> </a></td><td>Likely Oncogenic</td></tr><tr><td style="white-space:nowrap">vus<a name="variant-significance-codesystem-vus"> </a></td><td>VUS</td></tr><tr><td style="white-space:nowrap">likely_benign<a name="variant-significance-codesystem-likely_benign"> </a></td><td>Likely Benign</td></tr><tr><td style="white-space:nowrap">benign<a name="variant-significance-codesystem-benign"> </a></td><td>Benign</td></tr></table></div>
</text>
<url
value="http://fhir.genomoncology.io/CodeSystem/variant-significance-codesystem"/>
<version value="0.2.0"/>
<name value="VariantSignificance"/>
<title value="GenomOncology Variant Significance"/>
<status value="active"/>
<date value="2024-12-11T19:26:03+00:00"/>
<publisher value="GenomOncology"/>
<contact>
<name value="GenomOncology"/>
<telecom>
<system value="url"/>
<value value="http://genomoncology.com"/>
</telecom>
</contact>
<description value="Variant tiers tied to implications"/>
<content value="complete"/>
<count value="5"/>
<concept>
<code value="oncogenic"/>
<display value="Oncogenic"/>
</concept>
<concept>
<code value="likely_oncogenic"/>
<display value="Likely Oncogenic"/>
</concept>
<concept>
<code value="vus"/>
<display value="VUS"/>
</concept>
<concept>
<code value="likely_benign"/>
<display value="Likely Benign"/>
</concept>
<concept>
<code value="benign"/>
<display value="Benign"/>
</concept>
</CodeSystem>