{
"description": "A mapping between NCHS IJE and FHIR NewbornCongenitalAnomalies Value Sets",
"_filename": "ConceptMap-NewbornCongenitalAnomaliesCM.json",
"package_name": "hl7.fhir.us.bfdr.r4",
"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": "46ec4c1a-6cfd-49b0-9133-eb91e7eccabb",
"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"
} ]
} ]
}