Birth And Fetal Death (BFDR) FHIR Implementation Guide
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Birth And Fetal Death (BFDR) FHIR Implementation Guide, published by HL7 International / Public Health. This guide is not an authorized publication; it is the continuous build for version 2.0.0 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

: NewbornCongenitalAnomalies Concept Map - JSON Representation

Draft as of 2024-10-15

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{
  "resourceType" : "ConceptMap",
  "id" : "NewbornCongenitalAnomaliesCM",
  "text" : {
    "status" : "generated",
    "div" : "<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>"
  },
  "extension" : [
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
      "valueCode" : "pher"
    }
  ],
  "url" : "http://hl7.org/fhir/us/bfdr/ConceptMap/NewbornCongenitalAnomaliesCM",
  "identifier" : {
    "system" : "urn:ietf:rfc:3986",
    "value" : "urn:oid:2.16.840.1.113883.4.642.40.13.18.11"
  },
  "version" : "2.0.0",
  "name" : "NewbornCongenitalAnomalies",
  "title" : "NewbornCongenitalAnomalies Concept Map",
  "status" : "draft",
  "experimental" : false,
  "date" : "2024-10-15T13:57:58+00:00",
  "publisher" : "HL7 International / Public Health",
  "contact" : [
    {
      "name" : "HL7 International / Public Health",
      "telecom" : [
        {
          "system" : "url",
          "value" : "http://www.hl7.org/Special/committees/pher"
        }
      ]
    }
  ],
  "description" : "A mapping between NCHS IJE and FHIR NewbornCongenitalAnomalies Value Sets",
  "useContext" : [
    {
      "code" : {
        "system" : "http://terminology.hl7.org/CodeSystem/usage-context-type",
        "code" : "focus"
      },
      "valueCodeableConcept" : {
        "text" : "for IJE to FHIR alignment"
      }
    }
  ],
  "jurisdiction" : [
    {
      "coding" : [
        {
          "system" : "urn:iso:std:iso:3166",
          "code" : "US",
          "display" : "United States of America"
        }
      ]
    }
  ],
  "purpose" : "To help implementers map from IJE to FHIR Vocabulary",
  "sourceCanonical" : "http://hl7.org/fhir/us/vr-common-library/ValueSet/ValueSet-ije-vr",
  "targetCanonical" : "http://hl7.org/fhir/us/bfdr/ValueSet/ValueSet-newborn-congenital-anomalies",
  "group" : [
    {
      "source" : "http://hl7.org/fhir/us/vr-common-library/CodeSystem/codesystem-ije-vr",
      "target" : "http://snomed.info/sct",
      "element" : [
        {
          "code" : "ANEN",
          "display" : "Congenital Anomalies of the Newborn--Anencephaly",
          "target" : [
            {
              "code" : "89369001",
              "display" : "Anencephaly",
              "equivalence" : "equivalent"
            }
          ]
        },
        {
          "code" : "MNSB",
          "display" : "Congenital Anomalies of the Newborn--Meningomyelocele/Spina Bifida",
          "target" : [
            {
              "code" : "67531005",
              "display" : "Meningomyelocele/Spina bifida",
              "equivalence" : "equivalent"
            }
          ]
        },
        {
          "code" : "CCHD",
          "display" : "Congenital Anomalies of the Newborn--Cyanotic congenital heart disease",
          "target" : [
            {
              "code" : "12770006",
              "display" : "Cyanotic congenital heart disease",
              "equivalence" : "equivalent"
            }
          ]
        },
        {
          "code" : "CDH",
          "display" : "Congenital Anomalies of the Newborn--Congenital diaphragmatic hernia",
          "target" : [
            {
              "code" : "17190001",
              "display" : "Congenital diaphragmatic hernia",
              "equivalence" : "equivalent"
            }
          ]
        },
        {
          "code" : "OMPH",
          "display" : "Congenital Anomalies of the Newborn--Omphalocele",
          "target" : [
            {
              "code" : "18735004",
              "display" : "Omphalocele",
              "equivalence" : "equivalent"
            }
          ]
        },
        {
          "code" : "GAST",
          "display" : "Congenital Anomalies of the Newborn--Gastroschisis",
          "target" : [
            {
              "code" : "72951007",
              "display" : "Gastroschisis",
              "equivalence" : "equivalent"
            }
          ]
        },
        {
          "code" : "LIMB",
          "display" : "Congenital Anomalies of the Newborn--Limb Reduction Defect",
          "target" : [
            {
              "code" : "67341007",
              "display" : "Limb reduction defect (excluding congenital amputation and dwarfing syndromes)",
              "equivalence" : "equivalent"
            }
          ]
        },
        {
          "code" : "CL",
          "display" : "Congenital Anomalies of the Newborn--Cleft Lip with or without Cleft Palate",
          "target" : [
            {
              "code" : "80281008",
              "display" : "Cleft Lip with or without Cleft Palate",
              "equivalence" : "equivalent"
            }
          ]
        },
        {
          "code" : "CP",
          "display" : "Congenital Anomalies of the Newborn--Cleft Palate Alone",
          "target" : [
            {
              "code" : "87979003",
              "display" : "Cleft Palate alone",
              "equivalence" : "equivalent"
            }
          ]
        },
        {
          "code" : "DOWT",
          "display" : "Congenital Anomalies of the Newborn--Down Syndrome",
          "target" : [
            {
              "code" : "70156005",
              "display" : "Down Syndrome",
              "equivalence" : "equivalent"
            }
          ]
        },
        {
          "code" : "CDIT",
          "display" : "Congenital Anomalies of the Newborn--Suspected Chromosomal disorder",
          "target" : [
            {
              "code" : "409709004",
              "display" : "Suspected chromosomal disorder",
              "equivalence" : "equivalent"
            }
          ]
        },
        {
          "code" : "HYPO",
          "display" : "Congenital Anomalies of the Newborn--Hypospadias",
          "target" : [
            {
              "code" : "416010008",
              "display" : "Hypospadias",
              "equivalence" : "equivalent"
            }
          ]
        }
      ]
    }
  ]
}