Birth And Fetal Death (BFDR) - STU2-ballot
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This page is part of the Vital Records Birth and Fetal Death Reporting (v2.0.0-ballot: STU 2 Ballot 1) based on FHIR (HL7® FHIR® Standard) R4. The current version which supersedes this version is 1.1.0. For a full list of available versions, see the Directory of published versions

: ValueSet - Newborn Congenital Anomalies - XML Representation

Draft as of 2023-12-18

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<ValueSet xmlns="http://hl7.org/fhir">
  <id value="ValueSet-newborn-congenital-anomalies"/>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><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/89369001">89369001</a></td><td>Anencephalus</td></tr><tr><td><a href="http://snomed.info/id/67531005">67531005</a></td><td>Meningomyelocele/Spina bifida</td></tr><tr><td><a href="http://snomed.info/id/12770006">12770006</a></td><td>Cyanotic congenital heart disease</td></tr><tr><td><a href="http://snomed.info/id/17190001">17190001</a></td><td>Congenital diaphragmatic hernia</td></tr><tr><td><a href="http://snomed.info/id/18735004">18735004</a></td><td>Congenital omphalocele</td></tr><tr><td><a href="http://snomed.info/id/72951007">72951007</a></td><td>Gastroschisis</td></tr><tr><td><a href="http://snomed.info/id/67341007">67341007</a></td><td>Longitudinal deficiency of limb - Limb reduction defect (excluding congenital amputation and dwarfing syndromes)</td></tr><tr><td><a href="http://snomed.info/id/80281008">80281008</a></td><td>Cleft Lip with or without Cleft Palate</td></tr><tr><td><a href="http://snomed.info/id/87979003">87979003</a></td><td>Cleft palate</td></tr><tr><td><a href="http://snomed.info/id/70156005">70156005</a></td><td>Anomaly of chromosome pair 21</td></tr><tr><td><a href="http://snomed.info/id/409709004">409709004</a></td><td>Chromosomal disorder</td></tr><tr><td><a href="http://snomed.info/id/416010008">416010008</a></td><td>Hypospadias</td></tr><tr><td><a href="http://snomed.info/id/260413007">260413007</a></td><td>None</td></tr></table></li></ul></div>
  </text>
  <extension
             url="http://hl7.org/fhir/StructureDefinition/structuredefinition-wg">
    <valueCode value="pher"/>
  </extension>
  <url
       value="http://hl7.org/fhir/us/bfdr/ValueSet/ValueSet-newborn-congenital-anomalies"/>
  <version value="2.0.0-ballot"/>
  <name value="NewbornCongenitalAnomaliesVS"/>
  <title value="ValueSet - Newborn Congenital Anomalies"/>
  <status value="draft"/>
  <experimental value="false"/>
  <date value="2023-12-18T14:34:58+00:00"/>
  <publisher value="HL7 International / Public Health"/>
  <contact>
    <name value="HL7 International / Public Health"/>
    <telecom>
      <system value="url"/>
      <value value="http://www.hl7.org/Special/committees/pher"/>
    </telecom>
  </contact>
  <description
               value="The valueset contains codes to represent newborn congenital anomalies. This valueset is based on [PHVS_NewbornCongenitalAnomalies_NCHS](https://phinvads.cdc.gov/vads/ViewValueSet.action?id=BC64CB23-8210-4CE0-B2AE-F45169BBDC51)"/>
  <jurisdiction>
    <coding>
      <system value="urn:iso:std:iso:3166"/>
      <code value="US"/>
      <display value="United States of America"/>
    </coding>
  </jurisdiction>
  <copyright
             value="This value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement"/>
  <compose>
    <include>
      <system value="http://snomed.info/sct"/>
      <concept>
        <code value="89369001"/>
        <display value="Anencephalus"/>
      </concept>
      <concept>
        <code value="67531005"/>
        <display value="Meningomyelocele/Spina bifida"/>
      </concept>
      <concept>
        <code value="12770006"/>
        <display value="Cyanotic congenital heart disease"/>
      </concept>
      <concept>
        <code value="17190001"/>
        <display value="Congenital diaphragmatic hernia"/>
      </concept>
      <concept>
        <code value="18735004"/>
        <display value="Congenital omphalocele"/>
      </concept>
      <concept>
        <code value="72951007"/>
        <display value="Gastroschisis"/>
      </concept>
      <concept>
        <code value="67341007"/>
        <display
                 value="Longitudinal deficiency of limb - Limb reduction defect (excluding congenital amputation and dwarfing syndromes)"/>
      </concept>
      <concept>
        <code value="80281008"/>
        <display value="Cleft Lip with or without Cleft Palate"/>
      </concept>
      <concept>
        <code value="87979003"/>
        <display value="Cleft palate"/>
      </concept>
      <concept>
        <code value="70156005"/>
        <display value="Anomaly of chromosome pair 21"/>
      </concept>
      <concept>
        <code value="409709004"/>
        <display value="Chromosomal disorder"/>
      </concept>
      <concept>
        <code value="416010008"/>
        <display value="Hypospadias"/>
      </concept>
      <concept>
        <code value="260413007"/>
        <display value="None"/>
      </concept>
    </include>
  </compose>
</ValueSet>