FHIR IG analytics| Package | hl7.fhir.us.bfdr.r4 |
| Resource Type | ConceptMap |
| Id | ConceptMap-NewbornCongenitalAnomaliesCM.json |
| FHIR Version | R4 |
No resources found
No resources found
Note: links and images are rebased to the (stated) source
Generated Narrative: ConceptMap NewbornCongenitalAnomaliesCM
Mapping from ValueSet - Placeholder ValueSet for Interjurisdictional Exchange (IJE) in Vital Records to Newborn Congenital Anomalies
Group 1 Mapping from Code System - Placeholder Code System for IJE in Vital Records to SNOMED CT (all versions)
| Source Code | Relationship | Target Code |
| ANEN (Congenital Anomalies of the Newborn--Anencephaly) | is equivalent to | 89369001 (Anencephaly) |
| MNSB (Congenital Anomalies of the Newborn--Meningomyelocele/Spina Bifida) | is equivalent to | 67531005 (Meningomyelocele/Spina bifida) |
| CCHD (Congenital Anomalies of the Newborn--Cyanotic congenital heart disease) | is equivalent to | 12770006 (Cyanotic congenital heart disease) |
| CDH (Congenital Anomalies of the Newborn--Congenital diaphragmatic hernia) | is equivalent to | 17190001 (Congenital diaphragmatic hernia) |
| OMPH (Congenital Anomalies of the Newborn--Omphalocele) | is equivalent to | 18735004 (Omphalocele) |
| GAST (Congenital Anomalies of the Newborn--Gastroschisis) | is equivalent to | 72951007 (Gastroschisis) |
| LIMB (Congenital Anomalies of the Newborn--Limb Reduction Defect) | is equivalent to | 67341007 (Limb reduction defect (excluding congenital amputation and dwarfing syndromes)) |
| CL (Congenital Anomalies of the Newborn--Cleft Lip with or without Cleft Palate) | is equivalent to | 80281008 (Cleft Lip with or without Cleft Palate) |
| CP (Congenital Anomalies of the Newborn--Cleft Palate Alone) | is equivalent to | 87979003 (Cleft Palate alone) |
| DOWT (Congenital Anomalies of the Newborn--Down Syndrome) | is equivalent to | 70156005 (Down Syndrome) |
| CDIT (Congenital Anomalies of the Newborn--Suspected Chromosomal disorder) | is equivalent to | 409709004 (Suspected chromosomal disorder) |
| HYPO (Congenital Anomalies of the Newborn--Hypospadias) | is equivalent to | 416010008 (Hypospadias) |
FHIR
FHIRsmith{
"resourceType": "ConceptMap",
"id": "NewbornCongenitalAnomaliesCM",
"text": {
"status": "generated",
"div": "<!-- snip (see above) -->"
},
"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": "2024-10-15T15:43:14+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"
}
]
}
]
}
]
}