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

: NewbornCongenitalAnomalies Concept Map - TTL Representation

Draft as of 2023-12-18

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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:ConceptMap ;
  fhir:nodeRole fhir:treeRoot ;
  fhir:id [ fhir:v "NewbornCongenitalAnomaliesCM"] ; # 
  fhir:text [
fhir:status [ fhir:v "extensions" ] ;
fhir:div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p>Mapping from (not specified) to <a href=\"ValueSet-ValueSet-newborn-congenital-anomalies.html\">ValueSet - Newborn Congenital Anomalies</a></p><p>DRAFT. Published on 2023-12-18 14:34:58+0000 by HL7 International / Public Health (HL7 International / Public Health: <a href=\"http://www.hl7.org/Special/committees/pher\">http://www.hl7.org/Special/com...</a>). </p><div><p>A mapping between NCHS IJE and FHIR NewbornCongenitalAnomalies Value Sets</p>\n</div><br/><p><b>Group 1</b>Mapping from <a href=\"http://hl7.org/fhir/us/vr-common-library/2024Jan/CodeSystem-codesystem-ije-vr.html\">Placeholder Code System for IJE in Vital Records</a> to <a href=\"http://hl7.org/fhir/R4/codesystem-snomedct.html\">SNOMED CT (all versions)</a></p><table class=\"grid\"><tr><td><b>Source Code</b></td><td><b>Relationship</b></td><td><b>Target Code</b></td></tr><tr><td>ANEN (Congenital Anomalies of the Newborn--Anencephaly)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#null\"/></td><td>89369001 (Anencephaly)</td></tr><tr><td>MNSB (Congenital Anomalies of the Newborn--Meningomyelocele/Spina Bifida)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#null\"/></td><td>67531005 (Meningomyelocele/Spina bifida)</td></tr><tr><td>CCHD (Congenital Anomalies of the Newborn--Cyanotic congenital heart disease)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#null\"/></td><td>12770006 (Cyanotic congenital heart disease)</td></tr><tr><td>CDH (Congenital Anomalies of the Newborn--Congenital diaphragmatic hernia)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#null\"/></td><td>17190001 (Congenital diaphragmatic hernia)</td></tr><tr><td>OMPH (Congenital Anomalies of the Newborn--Omphalocele)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#null\"/></td><td>18735004 (Omphalocele)</td></tr><tr><td>GAST (Congenital Anomalies of the Newborn--Gastroschisis)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#null\"/></td><td>72951007 (Gastroschisis)</td></tr><tr><td>LIMB (Congenital Anomalies of the Newborn--Limb Reduction Defect)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#null\"/></td><td>67341007 (Limb reduction defect (excluding congenital amputation and dwarfing syndromes))</td></tr><tr><td>CL (Congenital Anomalies of the Newborn--Cleft Lip with or without Cleft Palate)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#null\"/></td><td>80281008 (Cleft Lip with or without Cleft Palate)</td></tr><tr><td>CP (Congenital Anomalies of the Newborn--Cleft Palate Alone)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#null\"/></td><td>87979003 (Cleft Palate alone)</td></tr><tr><td>DOWT (Congenital Anomalies of the Newborn--Down Syndrome)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#null\"/></td><td>70156005 (Down Syndrome)</td></tr><tr><td>CDIT (Congenital Anomalies of the Newborn--Suspected Chromosomal disorder)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#null\"/></td><td>409709004 (Suspected chromosomal disorder)</td></tr><tr><td>HYPO (Congenital Anomalies of the Newborn--Hypospadias)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#null\"/></td><td>416010008 (Hypospadias)</td></tr></table></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/ConceptMap/NewbornCongenitalAnomaliesCM"^^xsd:anyURI] ; # 
  fhir:version [ fhir:v "2.0.0-ballot"] ; # 
  fhir:name [ fhir:v "NewbornCongenitalAnomalies"] ; # 
  fhir:title [ fhir:v "NewbornCongenitalAnomalies Concept Map"] ; # 
  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 "A mapping between NCHS IJE and FHIR NewbornCongenitalAnomalies Value Sets"] ; # 
  fhir:useContext ( [
fhir:code [
fhir:system [ fhir:v "http://terminology.hl7.org/CodeSystem/usage-context-type"^^xsd:anyURI ] ;
fhir:code [ fhir:v "focus" ]     ] ;
fhir:value [
a fhir:CodeableConcept ;
fhir:text [ fhir:v "for IJE to FHIR alignment" ]     ]
  ] ) ; # 
  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:purpose [ fhir:v "To help implementers map from IJE to FHIR Vocabulary"] ; # 
  fhir:target [
fhir:v "http://hl7.org/fhir/us/bfdr/ValueSet/ValueSet-newborn-congenital-anomalies"^^xsd:anyURI ;
fhir:link <http://hl7.org/fhir/us/bfdr/ValueSet/ValueSet-newborn-congenital-anomalies>
  ] ; # 
  fhir:group ( [
fhir:source [ fhir:v "http://hl7.org/fhir/us/vr-common-library/CodeSystem/codesystem-ije-vr"^^xsd:anyURI ] ;
fhir:target [ fhir:v "http://snomed.info/sct"^^xsd:anyURI ] ;
    ( fhir:element [
fhir:code [ fhir:v "ANEN" ] ;
fhir:display [ fhir:v "Congenital Anomalies of the Newborn--Anencephaly" ] ;
      ( fhir:_target [
        ( fhir:modifierExtension [
fhir:url [ fhir:v "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence"^^xsd:anyURI ] ;
fhir:value [ fhir:v "equivalent" ]         ] ) ;
fhir:code [ fhir:v "89369001" ] ;
fhir:display [ fhir:v "Anencephaly" ] ;
fhir:equivalence [ fhir:v "equivalent" ]       ] )     ] [
fhir:code [ fhir:v "MNSB" ] ;
fhir:display [ fhir:v "Congenital Anomalies of the Newborn--Meningomyelocele/Spina Bifida" ] ;
      ( fhir:_target [
        ( fhir:modifierExtension [
fhir:url [ fhir:v "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence"^^xsd:anyURI ] ;
fhir:value [ fhir:v "equivalent" ]         ] ) ;
fhir:code [ fhir:v "67531005" ] ;
fhir:display [ fhir:v "Meningomyelocele/Spina bifida" ] ;
fhir:equivalence [ fhir:v "equivalent" ]       ] )     ] [
fhir:code [ fhir:v "CCHD" ] ;
fhir:display [ fhir:v "Congenital Anomalies of the Newborn--Cyanotic congenital heart disease" ] ;
      ( fhir:_target [
        ( fhir:modifierExtension [
fhir:url [ fhir:v "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence"^^xsd:anyURI ] ;
fhir:value [ fhir:v "equivalent" ]         ] ) ;
fhir:code [ fhir:v "12770006" ] ;
fhir:display [ fhir:v "Cyanotic congenital heart disease" ] ;
fhir:equivalence [ fhir:v "equivalent" ]       ] )     ] [
fhir:code [ fhir:v "CDH" ] ;
fhir:display [ fhir:v "Congenital Anomalies of the Newborn--Congenital diaphragmatic hernia" ] ;
      ( fhir:_target [
        ( fhir:modifierExtension [
fhir:url [ fhir:v "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence"^^xsd:anyURI ] ;
fhir:value [ fhir:v "equivalent" ]         ] ) ;
fhir:code [ fhir:v "17190001" ] ;
fhir:display [ fhir:v "Congenital diaphragmatic hernia" ] ;
fhir:equivalence [ fhir:v "equivalent" ]       ] )     ] [
fhir:code [ fhir:v "OMPH" ] ;
fhir:display [ fhir:v "Congenital Anomalies of the Newborn--Omphalocele" ] ;
      ( fhir:_target [
        ( fhir:modifierExtension [
fhir:url [ fhir:v "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence"^^xsd:anyURI ] ;
fhir:value [ fhir:v "equivalent" ]         ] ) ;
fhir:code [ fhir:v "18735004" ] ;
fhir:display [ fhir:v "Omphalocele" ] ;
fhir:equivalence [ fhir:v "equivalent" ]       ] )     ] [
fhir:code [ fhir:v "GAST" ] ;
fhir:display [ fhir:v "Congenital Anomalies of the Newborn--Gastroschisis" ] ;
      ( fhir:_target [
        ( fhir:modifierExtension [
fhir:url [ fhir:v "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence"^^xsd:anyURI ] ;
fhir:value [ fhir:v "equivalent" ]         ] ) ;
fhir:code [ fhir:v "72951007" ] ;
fhir:display [ fhir:v "Gastroschisis" ] ;
fhir:equivalence [ fhir:v "equivalent" ]       ] )     ] [
fhir:code [ fhir:v "LIMB" ] ;
fhir:display [ fhir:v "Congenital Anomalies of the Newborn--Limb Reduction Defect" ] ;
      ( fhir:_target [
        ( fhir:modifierExtension [
fhir:url [ fhir:v "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence"^^xsd:anyURI ] ;
fhir:value [ fhir:v "equivalent" ]         ] ) ;
fhir:code [ fhir:v "67341007" ] ;
fhir:display [ fhir:v "Limb reduction defect (excluding congenital amputation and dwarfing syndromes)" ] ;
fhir:equivalence [ fhir:v "equivalent" ]       ] )     ] [
fhir:code [ fhir:v "CL" ] ;
fhir:display [ fhir:v "Congenital Anomalies of the Newborn--Cleft Lip with or without Cleft Palate" ] ;
      ( fhir:_target [
        ( fhir:modifierExtension [
fhir:url [ fhir:v "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence"^^xsd:anyURI ] ;
fhir:value [ fhir:v "equivalent" ]         ] ) ;
fhir:code [ fhir:v "80281008" ] ;
fhir:display [ fhir:v "Cleft Lip with or without Cleft Palate" ] ;
fhir:equivalence [ fhir:v "equivalent" ]       ] )     ] [
fhir:code [ fhir:v "CP" ] ;
fhir:display [ fhir:v "Congenital Anomalies of the Newborn--Cleft Palate Alone" ] ;
      ( fhir:_target [
        ( fhir:modifierExtension [
fhir:url [ fhir:v "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence"^^xsd:anyURI ] ;
fhir:value [ fhir:v "equivalent" ]         ] ) ;
fhir:code [ fhir:v "87979003" ] ;
fhir:display [ fhir:v "Cleft Palate alone" ] ;
fhir:equivalence [ fhir:v "equivalent" ]       ] )     ] [
fhir:code [ fhir:v "DOWT" ] ;
fhir:display [ fhir:v "Congenital Anomalies of the Newborn--Down Syndrome" ] ;
      ( fhir:_target [
        ( fhir:modifierExtension [
fhir:url [ fhir:v "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence"^^xsd:anyURI ] ;
fhir:value [ fhir:v "equivalent" ]         ] ) ;
fhir:code [ fhir:v "70156005" ] ;
fhir:display [ fhir:v "Down Syndrome" ] ;
fhir:equivalence [ fhir:v "equivalent" ]       ] )     ] [
fhir:code [ fhir:v "CDIT" ] ;
fhir:display [ fhir:v "Congenital Anomalies of the Newborn--Suspected Chromosomal disorder" ] ;
      ( fhir:_target [
        ( fhir:modifierExtension [
fhir:url [ fhir:v "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence"^^xsd:anyURI ] ;
fhir:value [ fhir:v "equivalent" ]         ] ) ;
fhir:code [ fhir:v "409709004" ] ;
fhir:display [ fhir:v "Suspected chromosomal disorder" ] ;
fhir:equivalence [ fhir:v "equivalent" ]       ] )     ] [
fhir:code [ fhir:v "HYPO" ] ;
fhir:display [ fhir:v "Congenital Anomalies of the Newborn--Hypospadias" ] ;
      ( fhir:_target [
        ( fhir:modifierExtension [
fhir:url [ fhir:v "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence"^^xsd:anyURI ] ;
fhir:value [ fhir:v "equivalent" ]         ] ) ;
fhir:code [ fhir:v "416010008" ] ;
fhir:display [ fhir:v "Hypospadias" ] ;
fhir:equivalence [ fhir:v "equivalent" ]       ] )     ] )
  ] ) . #