Birth And Fetal Death (BFDR) - STU2-ballot
2.0.0-Preview1 - trial-use
Birth And Fetal Death (BFDR) - STU2-ballot
2.0.0-Preview1 - trial-use
Birth And Fetal Death (BFDR) - STU2-ballot, published by HL7 International / Public Health. This guide is not an authorized publication; it is the continuous build for version 2.0.0-Preview1 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/fhir-bfdr/ and changes regularly. See the Directory of published versions
| Active as of 2024-05-01 |
<ValueSet xmlns="http://hl7.org/fhir">
<id value="ValueSet-newborn-congenital-anomalies"/>
<text>
<status value="extensions"/>
<div xmlns="http://www.w3.org/1999/xhtml"><p>This value set includes codes based on the following rules:</p><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></table></li><li>Include these codes as defined in <a href="http://terminology.hl7.org/5.5.0/CodeSystem-v3-NullFlavor.html"><code>http://terminology.hl7.org/CodeSystem/v3-NullFlavor</code></a><table class="none"><tr><td style="white-space:nowrap"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td><a href="http://terminology.hl7.org/5.5.0/CodeSystem-v3-NullFlavor.html#v3-NullFlavor-OTH">OTH</a></td><td>Other</td><td>**Description:**The actual value is not a member of the set of permitted data values in the constrained value domain of a variable. (e.g., concept not provided by required code system).<br/><br/>**Usage Notes**: This flavor and its specializations are most commonly used with the CD datatype and its flavors. However, it may apply to \*any\* datatype where the constraints of the type are tighter than can be conveyed. For example, a PQ that is for a true measured amount whose units are not supported in UCUM, a need to convey a REAL when the type has been constrained to INT, etc.<br/><br/>With coded datatypes, this null flavor may only be used if the vocabulary binding has a coding strength of CNE. By definition, all local codes and original text are part of the value set if the coding strength is CWE.</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"/>
<identifier>
<system value="urn:ietf:rfc:3986"/>
<value value="urn:oid:2.16.840.1.113883.4.642.40.13.48.17"/>
</identifier>
<version value="2.0.0-Preview1"/>
<name value="NewbornCongenitalAnomaliesVS"/>
<title value="Newborn Congenital Anomalies"/>
<status value="active"/>
<experimental value="false"/>
<date value="2024-05-01T15:45:00+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). Includes 'Other' value for general utility, although #OTH is not allowed for birth submissions to NCHS."/>
<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>
</include>
<include>
<system value="http://terminology.hl7.org/CodeSystem/v3-NullFlavor"/>
<concept>
<code value="OTH"/>
<display value="Other"/>
</concept>
</include>
</compose>
</ValueSet>
IG © 2023+ HL7 International / Public Health. Package hl7.fhir.us.bfdr#2.0.0-Preview1 based on FHIR 4.0.1. Generated 2024-05-01
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