{ "description": "A mapping between NCHS IJE and FHIR NewbornCongenitalAnomalies Value Sets", "_filename": "ConceptMap-NewbornCongenitalAnomaliesCM.json", "package_name": "hl7.fhir.us.bfdr", "date": "2023-12-18T14:34:58+00:00", "group": [ { "source": "http://hl7.org/fhir/us/vr-common-library/CodeSystem/codesystem-ije-vr", "target": "http://snomed.info/sct", "element": [ { "code": "ANEN", "target": [ { "code": "89369001", "display": "Anencephaly", "equivalence": "equivalent", "modifierExtension": [ { "url": "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence", "valueCode": "equivalent" } ] } ], "display": "Congenital Anomalies of the Newborn--Anencephaly" }, { "code": "MNSB", "target": [ { "code": "67531005", "display": "Meningomyelocele/Spina bifida", "equivalence": "equivalent", "modifierExtension": [ { "url": "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence", "valueCode": "equivalent" } ] } ], "display": "Congenital Anomalies of the Newborn--Meningomyelocele/Spina Bifida" }, { "code": "CCHD", "target": [ { "code": "12770006", "display": "Cyanotic congenital heart disease", "equivalence": "equivalent", "modifierExtension": [ { "url": "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence", "valueCode": "equivalent" } ] } ], "display": "Congenital Anomalies of the Newborn--Cyanotic congenital heart disease" }, { "code": "CDH", "target": [ { "code": "17190001", "display": "Congenital diaphragmatic hernia", "equivalence": "equivalent", "modifierExtension": [ { "url": "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence", "valueCode": "equivalent" } ] } ], "display": "Congenital Anomalies of the Newborn--Congenital diaphragmatic hernia" }, { "code": "OMPH", "target": [ { "code": "18735004", "display": "Omphalocele", "equivalence": "equivalent", "modifierExtension": [ { "url": "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence", "valueCode": "equivalent" } ] } ], "display": "Congenital Anomalies of the Newborn--Omphalocele" }, { "code": "GAST", "target": [ { "code": "72951007", "display": "Gastroschisis", "equivalence": "equivalent", "modifierExtension": [ { "url": "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence", "valueCode": "equivalent" } ] } ], "display": "Congenital Anomalies of the Newborn--Gastroschisis" }, { "code": "LIMB", "target": [ { "code": "67341007", "display": "Limb reduction defect (excluding congenital amputation and dwarfing syndromes)", "equivalence": "equivalent", "modifierExtension": [ { "url": "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence", "valueCode": "equivalent" } ] } ], "display": "Congenital Anomalies of the Newborn--Limb Reduction Defect" }, { "code": "CL", "target": [ { "code": "80281008", "display": "Cleft Lip with or without Cleft Palate", "equivalence": "equivalent", "modifierExtension": [ { "url": "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence", "valueCode": "equivalent" } ] } ], "display": "Congenital Anomalies of the Newborn--Cleft Lip with or without Cleft Palate" }, { "code": "CP", "target": [ { "code": "87979003", "display": "Cleft Palate alone", "equivalence": "equivalent", "modifierExtension": [ { "url": "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence", "valueCode": "equivalent" } ] } ], "display": "Congenital Anomalies of the Newborn--Cleft Palate Alone" }, { "code": "DOWT", "target": [ { "code": "70156005", "display": "Down Syndrome", "equivalence": "equivalent", "modifierExtension": [ { "url": "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence", "valueCode": "equivalent" } ] } ], "display": "Congenital Anomalies of the Newborn--Down Syndrome" }, { "code": "CDIT", "target": [ { "code": "409709004", "display": "Suspected chromosomal disorder", "equivalence": "equivalent", "modifierExtension": [ { "url": "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence", "valueCode": "equivalent" } ] } ], "display": "Congenital Anomalies of the Newborn--Suspected Chromosomal disorder" }, { "code": "HYPO", "target": [ { "code": "416010008", "display": "Hypospadias", "equivalence": "equivalent", "modifierExtension": [ { "url": "http://hl7.org/fhir/1.0/StructureDefinition/extension-ConceptMap.element.target.equivalence", "valueCode": "equivalent" } ] } ], "display": "Congenital Anomalies of the Newborn--Hypospadias" } ] } ], "publisher": "HL7 International / Public Health", "jurisdiction": [ { "coding": [ { "code": "US", "system": "urn:iso:std:iso:3166", "display": "United States of America" } ] } ], "purpose": "To help implementers map from IJE to FHIR Vocabulary", "name": "NewbornCongenitalAnomalies", "useContext": [ { "code": { "code": "focus", "system": "http://terminology.hl7.org/CodeSystem/usage-context-type" }, "valueCodeableConcept": { "text": "for IJE to FHIR alignment" } } ], "type": null, "experimental": "false", "resourceType": "ConceptMap", "title": "NewbornCongenitalAnomalies Concept Map", "package_version": "2.0.0-ballot", "extension": [ { "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg", "valueCode": "pher" } ], "targetCanonical": "http://hl7.org/fhir/us/bfdr/ValueSet/ValueSet-newborn-congenital-anomalies", "status": "draft", "id": "a505d977-cc59-4f22-9556-ebc03ad64d9f", "kind": null, "url": "http://hl7.org/fhir/us/bfdr/ConceptMap/NewbornCongenitalAnomaliesCM", "version": "2.0.0-ballot", "contact": [ { "name": "HL7 International / Public Health", "telecom": [ { "value": "http://www.hl7.org/Special/committees/pher", "system": "url" } ] } ] }