| Package | hl7.fhir.us.bfdr |
| Type | ConceptMap |
| Id | Id |
| 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 | 2024-10-15T13:57:58+00:00 |
| Name | NewbornCongenitalAnomalies |
| Title | NewbornCongenitalAnomalies Concept Map |
| Experimental | False |
| 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 | |
http://hl7.org/fhir/us/vr-common-library/CodeSystem/codesystem-ije-vr  | Code System - Placeholder Code System for IJE in Vital Records |
| http://snomed.info/sct | SNOMED CT (all versions) |
| http://snomed.info/sct | SNOMED codes used in this IG |
| http://snomed.info/sct | SNOMED CT Canada Immunizations |
| http://hl7.org/fhir/us/vr-common-library/ValueSet/ValueSet-ije-vr | ValueSet - Placeholder ValueSet for Interjurisdictional Exchange (IJE) in Vital Records |
| http://hl7.org/fhir/us/bfdr/ValueSet/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) |
FHIR{
"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"
}
]
}
]
}
]
}
XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.