Package | hl7.fhir.us.bfdr |
Type | ConceptMap |
Id | NewbornCongenitalAnomaliesCM |
FHIR Version | R4 |
Source | http://hl7.org/fhir/us/bfdr/https://build.fhir.org/ig/HL7/fhir-bfdr/ConceptMap-NewbornCongenitalAnomaliesCM.html |
URL | http://hl7.org/fhir/us/bfdr/ConceptMap/NewbornCongenitalAnomaliesCM |
Version | 2.0.0 |
Status | draft |
Date | 2025-02-19T23:13:54+00:00 |
Name | NewbornCongenitalAnomalies |
Title | NewbornCongenitalAnomalies Concept Map |
Realm | us |
Authority | hl7 |
Description | A mapping between NCHS IJE and FHIR NewbornCongenitalAnomalies Value Sets |
Purpose | To help implementers map from IJE to FHIR Vocabulary |
No resources found
CodeSystem | |
codesystem-ije-vr | Code System - Placeholder Code System for IJE in Vital Records |
sct | SNOMED CT (all versions) |
sct | SNOMED codes used in this IG |
sct | veri |
ValueSet | |
ValueSet-ije-vr | ValueSet - Placeholder ValueSet for Interjurisdictional Exchange (IJE) in Vital Records |
ValueSet-newborn-congenital-anomalies | Newborn Congenital Anomalies |
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) |
{ "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": "2025-02-19T23:13:54+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" } ] } ] } ] }