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 - TTL Representation
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@prefix fhir: <http://hl7.org/fhir/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
# - resource -------------------------------------------------------------------
a fhir:ValueSet ;
fhir:nodeRole fhir:treeRoot ;
fhir:id [ fhir:v "ValueSet-newborn-congenital-anomalies"] ; #
fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div "<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>"
] ; #
fhir:extension ( [
fhir:url [ fhir:v "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg"^^xsd:anyURI ] ;
fhir:value [ fhir:v "pher" ]
] ) ; #
fhir:url [ fhir:v "http://hl7.org/fhir/us/bfdr/ValueSet/ValueSet-newborn-congenital-anomalies"^^xsd:anyURI] ; #
fhir:version [ fhir:v "2.0.0-ballot"] ; #
fhir:name [ fhir:v "NewbornCongenitalAnomaliesVS"] ; #
fhir:title [ fhir:v "ValueSet - Newborn Congenital Anomalies"] ; #
fhir:status [ fhir:v "draft"] ; #
fhir:experimental [ fhir:v "false"^^xsd:boolean] ; #
fhir:date [ fhir:v "2023-12-18T14:34:58+00:00"^^xsd:dateTime] ; #
fhir:publisher [ fhir:v "HL7 International / Public Health"] ; #
fhir:contact ( [
fhir:name [ fhir:v "HL7 International / Public Health" ] ;
( fhir:telecom [
fhir:system [ fhir:v "url" ] ;
fhir:value [ fhir:v "http://www.hl7.org/Special/committees/pher" ] ] )
] ) ; #
fhir:description [ fhir:v "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)"] ; #
fhir:jurisdiction ( [
( fhir:coding [
fhir:system [ fhir:v "urn:iso:std:iso:3166"^^xsd:anyURI ] ;
fhir:code [ fhir:v "US" ] ;
fhir:display [ fhir:v "United States of America" ] ] )
] ) ; #
fhir:copyright [ fhir:v "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"] ; #
fhir:compose [
( fhir:include [
fhir:system [ fhir:v "http://snomed.info/sct"^^xsd:anyURI ] ;
( fhir:concept [
fhir:code [ fhir:v "89369001" ] ;
fhir:display [ fhir:v "Anencephalus" ] ] [
fhir:code [ fhir:v "67531005" ] ;
fhir:display [ fhir:v "Meningomyelocele/Spina bifida" ] ] [
fhir:code [ fhir:v "12770006" ] ;
fhir:display [ fhir:v "Cyanotic congenital heart disease" ] ] [
fhir:code [ fhir:v "17190001" ] ;
fhir:display [ fhir:v "Congenital diaphragmatic hernia" ] ] [
fhir:code [ fhir:v "18735004" ] ;
fhir:display [ fhir:v "Congenital omphalocele" ] ] [
fhir:code [ fhir:v "72951007" ] ;
fhir:display [ fhir:v "Gastroschisis" ] ] [
fhir:code [ fhir:v "67341007" ] ;
fhir:display [ fhir:v "Longitudinal deficiency of limb - Limb reduction defect (excluding congenital amputation and dwarfing syndromes)" ] ] [
fhir:code [ fhir:v "80281008" ] ;
fhir:display [ fhir:v "Cleft Lip with or without Cleft Palate" ] ] [
fhir:code [ fhir:v "87979003" ] ;
fhir:display [ fhir:v "Cleft palate" ] ] [
fhir:code [ fhir:v "70156005" ] ;
fhir:display [ fhir:v "Anomaly of chromosome pair 21" ] ] [
fhir:code [ fhir:v "409709004" ] ;
fhir:display [ fhir:v "Chromosomal disorder" ] ] [
fhir:code [ fhir:v "416010008" ] ;
fhir:display [ fhir:v "Hypospadias" ] ] [
fhir:code [ fhir:v "260413007" ] ;
fhir:display [ fhir:v "None" ] ] ) ] )
] . #
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