Birth And Fetal Death (BFDR) FHIR Implementation Guide
2.0.0 - STU2
Birth And Fetal Death (BFDR) FHIR Implementation Guide
2.0.0 - STU2
This page is part of the Vital Records Birth and Fetal Death Reporting (v2.0.0: STU2) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions
| Draft as of 2024-10-15 |
<ConceptMap xmlns="http://hl7.org/fhir">
<id value="NewbornCongenitalAnomaliesCM"/>
<text>
<status value="generated"/>
<div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: ConceptMap NewbornCongenitalAnomaliesCM</b></p><a name="NewbornCongenitalAnomaliesCM"> </a><a name="hcNewbornCongenitalAnomaliesCM"> </a><a name="NewbornCongenitalAnomaliesCM-en-US"> </a><p>Mapping from <a href="http://hl7.org/fhir/us/vr-common-library/STU2/ValueSet-ValueSet-ije-vr.html">ValueSet - Placeholder ValueSet for Interjurisdictional Exchange (IJE) in Vital Records</a> to <a href="ValueSet-ValueSet-newborn-congenital-anomalies.html">Newborn Congenital Anomalies</a></p><br/><p><b>Group 1 </b>Mapping from <a href="http://hl7.org/fhir/us/vr-common-library/STU2/CodeSystem-codesystem-ije-vr.html">Code System - 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/extensions/5.1.0/CodeSystem-concept-map-equivalence.html#equivalent" title="equivalent">is equivalent to</a></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/extensions/5.1.0/CodeSystem-concept-map-equivalence.html#equivalent" title="equivalent">is equivalent to</a></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/extensions/5.1.0/CodeSystem-concept-map-equivalence.html#equivalent" title="equivalent">is equivalent to</a></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/extensions/5.1.0/CodeSystem-concept-map-equivalence.html#equivalent" title="equivalent">is equivalent to</a></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/extensions/5.1.0/CodeSystem-concept-map-equivalence.html#equivalent" title="equivalent">is equivalent to</a></td><td>18735004 (Omphalocele)</td></tr><tr><td>GAST (Congenital Anomalies of the Newborn--Gastroschisis)</td><td><a href="http://hl7.org/fhir/extensions/5.1.0/CodeSystem-concept-map-equivalence.html#equivalent" title="equivalent">is equivalent to</a></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/extensions/5.1.0/CodeSystem-concept-map-equivalence.html#equivalent" title="equivalent">is equivalent to</a></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/extensions/5.1.0/CodeSystem-concept-map-equivalence.html#equivalent" title="equivalent">is equivalent to</a></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/extensions/5.1.0/CodeSystem-concept-map-equivalence.html#equivalent" title="equivalent">is equivalent to</a></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/extensions/5.1.0/CodeSystem-concept-map-equivalence.html#equivalent" title="equivalent">is equivalent to</a></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/extensions/5.1.0/CodeSystem-concept-map-equivalence.html#equivalent" title="equivalent">is equivalent to</a></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/extensions/5.1.0/CodeSystem-concept-map-equivalence.html#equivalent" title="equivalent">is equivalent to</a></td><td>416010008 (Hypospadias)</td></tr></table></div>
</text>
<extension
url="http://hl7.org/fhir/StructureDefinition/structuredefinition-wg">
<valueCode value="pher"/>
</extension>
<url
value="http://hl7.org/fhir/us/bfdr/ConceptMap/NewbornCongenitalAnomaliesCM"/>
<identifier>
<system value="urn:ietf:rfc:3986"/>
<value value="urn:oid:2.16.840.1.113883.4.642.40.13.18.11"/>
</identifier>
<version value="2.0.0"/>
<name value="NewbornCongenitalAnomalies"/>
<title value="NewbornCongenitalAnomalies Concept Map"/>
<status value="draft"/>
<experimental value="false"/>
<date value="2024-10-15T14:34:26+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="A mapping between NCHS IJE and FHIR NewbornCongenitalAnomalies Value Sets"/>
<useContext>
<code>
<system
value="http://terminology.hl7.org/CodeSystem/usage-context-type"/>
<code value="focus"/>
</code>
<valueCodeableConcept>
<text value="for IJE to FHIR alignment"/>
</valueCodeableConcept>
</useContext>
<jurisdiction>
<coding>
<system value="urn:iso:std:iso:3166"/>
<code value="US"/>
<display value="United States of America"/>
</coding>
</jurisdiction>
<purpose value="To help implementers map from IJE to FHIR Vocabulary"/>
<sourceCanonical
value="http://hl7.org/fhir/us/vr-common-library/ValueSet/ValueSet-ije-vr"/>
<targetCanonical
value="http://hl7.org/fhir/us/bfdr/ValueSet/ValueSet-newborn-congenital-anomalies"/>
<group>
<source
value="http://hl7.org/fhir/us/vr-common-library/CodeSystem/codesystem-ije-vr"/>
<target value="http://snomed.info/sct"/>
<element>
<code value="ANEN"/>
<display value="Congenital Anomalies of the Newborn--Anencephaly"/>
<target>
<code value="89369001"/>
<display value="Anencephaly"/>
<equivalence value="equivalent"/>
</target>
</element>
<element>
<code value="MNSB"/>
<display
value="Congenital Anomalies of the Newborn--Meningomyelocele/Spina Bifida"/>
<target>
<code value="67531005"/>
<display value="Meningomyelocele/Spina bifida"/>
<equivalence value="equivalent"/>
</target>
</element>
<element>
<code value="CCHD"/>
<display
value="Congenital Anomalies of the Newborn--Cyanotic congenital heart disease"/>
<target>
<code value="12770006"/>
<display value="Cyanotic congenital heart disease"/>
<equivalence value="equivalent"/>
</target>
</element>
<element>
<code value="CDH"/>
<display
value="Congenital Anomalies of the Newborn--Congenital diaphragmatic hernia"/>
<target>
<code value="17190001"/>
<display value="Congenital diaphragmatic hernia"/>
<equivalence value="equivalent"/>
</target>
</element>
<element>
<code value="OMPH"/>
<display value="Congenital Anomalies of the Newborn--Omphalocele"/>
<target>
<code value="18735004"/>
<display value="Omphalocele"/>
<equivalence value="equivalent"/>
</target>
</element>
<element>
<code value="GAST"/>
<display value="Congenital Anomalies of the Newborn--Gastroschisis"/>
<target>
<code value="72951007"/>
<display value="Gastroschisis"/>
<equivalence value="equivalent"/>
</target>
</element>
<element>
<code value="LIMB"/>
<display
value="Congenital Anomalies of the Newborn--Limb Reduction Defect"/>
<target>
<code value="67341007"/>
<display
value="Limb reduction defect (excluding congenital amputation and dwarfing syndromes)"/>
<equivalence value="equivalent"/>
</target>
</element>
<element>
<code value="CL"/>
<display
value="Congenital Anomalies of the Newborn--Cleft Lip with or without Cleft Palate"/>
<target>
<code value="80281008"/>
<display value="Cleft Lip with or without Cleft Palate"/>
<equivalence value="equivalent"/>
</target>
</element>
<element>
<code value="CP"/>
<display
value="Congenital Anomalies of the Newborn--Cleft Palate Alone"/>
<target>
<code value="87979003"/>
<display value="Cleft Palate alone"/>
<equivalence value="equivalent"/>
</target>
</element>
<element>
<code value="DOWT"/>
<display value="Congenital Anomalies of the Newborn--Down Syndrome"/>
<target>
<code value="70156005"/>
<display value="Down Syndrome"/>
<equivalence value="equivalent"/>
</target>
</element>
<element>
<code value="CDIT"/>
<display
value="Congenital Anomalies of the Newborn--Suspected Chromosomal disorder"/>
<target>
<code value="409709004"/>
<display value="Suspected chromosomal disorder"/>
<equivalence value="equivalent"/>
</target>
</element>
<element>
<code value="HYPO"/>
<display value="Congenital Anomalies of the Newborn--Hypospadias"/>
<target>
<code value="416010008"/>
<display value="Hypospadias"/>
<equivalence value="equivalent"/>
</target>
</element>
</group>
</ConceptMap>
IG © 2023+ HL7 International / Public Health. Package hl7.fhir.us.bfdr#2.0.0 based on FHIR 4.0.1. Generated 2024-10-15
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