HSAI FHIR Implementation Guide
0.1.0 - CI Build Netherlands

HSAI FHIR Implementation Guide - Local Development build (v0.1.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions

## : CDT Condition Value Set - XML Representation

Active as of 2026-02-09

Raw xml | Download

    <ValueSet xmlns="http://hl7.org/fhir">
      <id value="cdt-condition-vs"/>
      <text>
        <status value="generated"/>
        <div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: ValueSet cdt-condition-vs</b></p><a name="cdt-condition-vs"> </a><a name="hccdt-condition-vs"> </a><a name="cdt-condition-vs-en"> </a><ul><li>Include these codes as defined in <a href="http://www.snomed.org/"><code>http://snomed.info/sct</code></a><table class="none"><tr><td style="white-space:nowrap"><b>Code</b></td><td><b>Display</b></td></tr><tr><td><a href="http://snomed.info/id/6002006">6002006</a></td><td>10p partial monosomy syndrome</td></tr><tr><td><a href="http://snomed.info/id/48760005">48760005</a></td><td>10p partial trisomy syndrome</td></tr><tr><td><a href="http://snomed.info/id/16129004">16129004</a></td><td>10q partial monosomy</td></tr><tr><td><a href="http://snomed.info/id/73035005">73035005</a></td><td>10q partial trisomy syndrome</td></tr><tr><td><a href="http://snomed.info/id/770401007">770401007</a></td><td>10q22.3q23.3 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/782669004">782669004</a></td><td>10q22.3q23.3 microduplication syndrome</td></tr><tr><td><a href="http://snomed.info/id/4135001">4135001</a></td><td>11p partial monosomy syndrome</td></tr><tr><td><a href="http://snomed.info/id/26480007">26480007</a></td><td>11p partial trisomy syndrome</td></tr><tr><td><a href="http://snomed.info/id/880078001">880078001</a></td><td>11p15 deletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/880079009">880079009</a></td><td>11p15 duplication syndrome</td></tr><tr><td><a href="http://snomed.info/id/770794008">770794008</a></td><td>11p15.4 microduplication syndrome</td></tr><tr><td><a href="http://snomed.info/id/4325000">4325000</a></td><td>11q partial monosomy syndrome</td></tr><tr><td><a href="http://snomed.info/id/4874006">4874006</a></td><td>11q partial trisomy syndrome</td></tr><tr><td><a href="http://snomed.info/id/1229882003">1229882003</a></td><td>11q22.2q22.3 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/14091009">14091009</a></td><td>12p partial trisomy syndrome</td></tr><tr><td><a href="http://snomed.info/id/778007004">778007004</a></td><td>12p12.1 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/40389006">40389006</a></td><td>12q partial trisomy syndrome</td></tr><tr><td><a href="http://snomed.info/id/719046005">719046005</a></td><td>12q14 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/880081006">880081006</a></td><td>12q15 deletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/734030009">734030009</a></td><td>12q15q21.1 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/880086001">880086001</a></td><td>12q24.31-q24.32 deletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/548004">548004</a></td><td>13p partial trisomy syndrome</td></tr><tr><td><a href="http://snomed.info/id/29257000">29257000</a></td><td>13q partial monosomy syndrome</td></tr><tr><td><a href="http://snomed.info/id/10572007">10572007</a></td><td>13q partial trisomy syndrome</td></tr><tr><td><a href="http://snomed.info/id/773547003">773547003</a></td><td>13q12.3 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/20348002">20348002</a></td><td>14q partial distal trisomy syndrome</td></tr><tr><td><a href="http://snomed.info/id/83585001">83585001</a></td><td>14q partial proximal trisomy syndrome</td></tr><tr><td><a href="http://snomed.info/id/7586009">7586009</a></td><td>14q partial trisomy</td></tr><tr><td><a href="http://snomed.info/id/719047001">719047001</a></td><td>14q11.2 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/771341006">771341006</a></td><td>14q11.2 microduplication syndrome</td></tr><tr><td><a href="http://snomed.info/id/719574007">719574007</a></td><td>14q12 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/771439009">771439009</a></td><td>14q22q23 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/773494008">773494008</a></td><td>14q24.1q24.3 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/1234830005">1234830005</a></td><td>14q32 duplication syndrome</td></tr><tr><td><a href="http://snomed.info/id/771477003">771477003</a></td><td>15q overgrowth syndrome</td></tr><tr><td><a href="http://snomed.info/id/771340007">771340007</a></td><td>15q11.2 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/719427001">719427001</a></td><td>15q11q13 microduplication syndrome</td></tr><tr><td><a href="http://snomed.info/id/699254009">699254009</a></td><td>15q13.3 microdeletion</td></tr><tr><td><a href="http://snomed.info/id/768713003">768713003</a></td><td>15q13.3 microduplication syndrome</td></tr><tr><td><a href="http://snomed.info/id/719575008">719575008</a></td><td>15q14 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/699308002">699308002</a></td><td>15q24 microdeletion</td></tr><tr><td><a href="http://snomed.info/id/719576009">719576009</a></td><td>16p11.2p12.2 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/733518000">733518000</a></td><td>16p11.2p12.2 microduplication syndrome</td></tr><tr><td><a href="http://snomed.info/id/1251450006">1251450006</a></td><td>16p12.1p12.3 triplication syndrome</td></tr><tr><td><a href="http://snomed.info/id/768471006">768471006</a></td><td>16p12.2 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/719577000">719577000</a></td><td>16p13.11 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/719578005">719578005</a></td><td>16p13.11 microduplication syndrome</td></tr><tr><td><a href="http://snomed.info/id/733473000">733473000</a></td><td>16p13.3 microduplication syndrome</td></tr><tr><td><a href="http://snomed.info/id/770760006">770760006</a></td><td>16q24.1 microdeletion syndrome</td></tr><tr><td><a href="http://snomed.info/id/719580004">719580004</a></td><td>16q24.3 microdeletion syndrome</td></tr></table></li></ul></div>
      </text>
      <url value="https://cdt-beta.healthsage.ai/fhir/ValueSet/cdt-condition-vs"/>
      <version value="0.1.0"/>
      <name value="CDTConditionVS"/>
      <title value="CDT Condition Value Set"/>
      <status value="active"/>
      <experimental value="false"/>
      <date value="2026-02-09T15:01:17+00:00"/>
      <publisher value="HealthSage AI"/>
      <contact>
        <name value="HealthSage AI"/>
        <telecom>
          <system value="url"/>
          <value value="https://healthsage.ai/"/>
        </telecom>
        <telecom>
          <system value="email"/>
          <value value="hello@healthsage.ai"/>
        </telecom>
      </contact>
      <contact>
        <name value="HealthSage AI"/>
        <telecom>
          <system value="email"/>
          <value value="hello@healthsage.ai"/>
          <use value="work"/>
        </telecom>
      </contact>
      <description
                   value="Value set containing condition codes from SNOMED CT for international use"/>
      <jurisdiction>
        <coding>
          <system value="urn:iso:std:iso:3166"/>
          <code value="NL"/>
          <display value="Netherlands"/>
        </coding>
      </jurisdiction>
      <compose>
        <include>
          <system value="http://snomed.info/sct"/>
          <concept>
            <code value="6002006"/>
            <display value="10p partial monosomy syndrome"/>
          </concept>
          <concept>
            <code value="48760005"/>
            <display value="10p partial trisomy syndrome"/>
          </concept>
          <concept>
            <code value="16129004"/>
            <display value="10q partial monosomy"/>
          </concept>
          <concept>
            <code value="73035005"/>
            <display value="10q partial trisomy syndrome"/>
          </concept>
          <concept>
            <code value="770401007"/>
            <display value="10q22.3q23.3 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="782669004"/>
            <display value="10q22.3q23.3 microduplication syndrome"/>
          </concept>
          <concept>
            <code value="4135001"/>
            <display value="11p partial monosomy syndrome"/>
          </concept>
          <concept>
            <code value="26480007"/>
            <display value="11p partial trisomy syndrome"/>
          </concept>
          <concept>
            <code value="880078001"/>
            <display value="11p15 deletion syndrome"/>
          </concept>
          <concept>
            <code value="880079009"/>
            <display value="11p15 duplication syndrome"/>
          </concept>
          <concept>
            <code value="770794008"/>
            <display value="11p15.4 microduplication syndrome"/>
          </concept>
          <concept>
            <code value="4325000"/>
            <display value="11q partial monosomy syndrome"/>
          </concept>
          <concept>
            <code value="4874006"/>
            <display value="11q partial trisomy syndrome"/>
          </concept>
          <concept>
            <code value="1229882003"/>
            <display value="11q22.2q22.3 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="14091009"/>
            <display value="12p partial trisomy syndrome"/>
          </concept>
          <concept>
            <code value="778007004"/>
            <display value="12p12.1 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="40389006"/>
            <display value="12q partial trisomy syndrome"/>
          </concept>
          <concept>
            <code value="719046005"/>
            <display value="12q14 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="880081006"/>
            <display value="12q15 deletion syndrome"/>
          </concept>
          <concept>
            <code value="734030009"/>
            <display value="12q15q21.1 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="880086001"/>
            <display value="12q24.31-q24.32 deletion syndrome"/>
          </concept>
          <concept>
            <code value="548004"/>
            <display value="13p partial trisomy syndrome"/>
          </concept>
          <concept>
            <code value="29257000"/>
            <display value="13q partial monosomy syndrome"/>
          </concept>
          <concept>
            <code value="10572007"/>
            <display value="13q partial trisomy syndrome"/>
          </concept>
          <concept>
            <code value="773547003"/>
            <display value="13q12.3 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="20348002"/>
            <display value="14q partial distal trisomy syndrome"/>
          </concept>
          <concept>
            <code value="83585001"/>
            <display value="14q partial proximal trisomy syndrome"/>
          </concept>
          <concept>
            <code value="7586009"/>
            <display value="14q partial trisomy"/>
          </concept>
          <concept>
            <code value="719047001"/>
            <display value="14q11.2 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="771341006"/>
            <display value="14q11.2 microduplication syndrome"/>
          </concept>
          <concept>
            <code value="719574007"/>
            <display value="14q12 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="771439009"/>
            <display value="14q22q23 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="773494008"/>
            <display value="14q24.1q24.3 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="1234830005"/>
            <display value="14q32 duplication syndrome"/>
          </concept>
          <concept>
            <code value="771477003"/>
            <display value="15q overgrowth syndrome"/>
          </concept>
          <concept>
            <code value="771340007"/>
            <display value="15q11.2 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="719427001"/>
            <display value="15q11q13 microduplication syndrome"/>
          </concept>
          <concept>
            <code value="699254009"/>
            <display value="15q13.3 microdeletion"/>
          </concept>
          <concept>
            <code value="768713003"/>
            <display value="15q13.3 microduplication syndrome"/>
          </concept>
          <concept>
            <code value="719575008"/>
            <display value="15q14 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="699308002"/>
            <display value="15q24 microdeletion"/>
          </concept>
          <concept>
            <code value="719576009"/>
            <display value="16p11.2p12.2 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="733518000"/>
            <display value="16p11.2p12.2 microduplication syndrome"/>
          </concept>
          <concept>
            <code value="1251450006"/>
            <display value="16p12.1p12.3 triplication syndrome"/>
          </concept>
          <concept>
            <code value="768471006"/>
            <display value="16p12.2 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="719577000"/>
            <display value="16p13.11 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="719578005"/>
            <display value="16p13.11 microduplication syndrome"/>
          </concept>
          <concept>
            <code value="733473000"/>
            <display value="16p13.3 microduplication syndrome"/>
          </concept>
          <concept>
            <code value="770760006"/>
            <display value="16q24.1 microdeletion syndrome"/>
          </concept>
          <concept>
            <code value="719580004"/>
            <display value="16q24.3 microdeletion syndrome"/>
          </concept>
        </include>
      </compose>
    </ValueSet>