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FHIR IG Statistics: ConceptMap/NewbornCongenitalAnomaliesCM

Packagehl7.fhir.us.bfdr
TypeConceptMap
IdNewbornCongenitalAnomaliesCM
FHIR VersionR4
Sourcehttp://hl7.org/fhir/us/bfdr/https://build.fhir.org/ig/HL7/fhir-bfdr/ConceptMap-NewbornCongenitalAnomaliesCM.html
URLhttp://hl7.org/fhir/us/bfdr/ConceptMap/NewbornCongenitalAnomaliesCM
Version2.0.0
Statusdraft
Date2025-02-19T23:13:54+00:00
NameNewbornCongenitalAnomalies
TitleNewbornCongenitalAnomalies Concept Map
Realmus
Authorityhl7
DescriptionA mapping between NCHS IJE and FHIR NewbornCongenitalAnomalies Value Sets
PurposeTo help implementers map from IJE to FHIR Vocabulary

Resources that use this resource

No resources found


Resources that this resource uses

CodeSystem
codesystem-ije-vrCode System - Placeholder Code System for IJE in Vital Records
sctSNOMED CT (all versions)
sctSNOMED codes used in this IG
sctveri
ValueSet
ValueSet-ije-vrValueSet - Placeholder ValueSet for Interjurisdictional Exchange (IJE) in Vital Records
ValueSet-newborn-congenital-anomaliesNewborn Congenital Anomalies

Narrative

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 CodeRelationshipTarget Code
ANEN (Congenital Anomalies of the Newborn--Anencephaly)is equivalent to89369001 (Anencephaly)
MNSB (Congenital Anomalies of the Newborn--Meningomyelocele/Spina Bifida)is equivalent to67531005 (Meningomyelocele/Spina bifida)
CCHD (Congenital Anomalies of the Newborn--Cyanotic congenital heart disease)is equivalent to12770006 (Cyanotic congenital heart disease)
CDH (Congenital Anomalies of the Newborn--Congenital diaphragmatic hernia)is equivalent to17190001 (Congenital diaphragmatic hernia)
OMPH (Congenital Anomalies of the Newborn--Omphalocele)is equivalent to18735004 (Omphalocele)
GAST (Congenital Anomalies of the Newborn--Gastroschisis)is equivalent to72951007 (Gastroschisis)
LIMB (Congenital Anomalies of the Newborn--Limb Reduction Defect)is equivalent to67341007 (Limb reduction defect (excluding congenital amputation and dwarfing syndromes))
CL (Congenital Anomalies of the Newborn--Cleft Lip with or without Cleft Palate)is equivalent to80281008 (Cleft Lip with or without Cleft Palate)
CP (Congenital Anomalies of the Newborn--Cleft Palate Alone)is equivalent to87979003 (Cleft Palate alone)
DOWT (Congenital Anomalies of the Newborn--Down Syndrome)is equivalent to70156005 (Down Syndrome)
CDIT (Congenital Anomalies of the Newborn--Suspected Chromosomal disorder)is equivalent to409709004 (Suspected chromosomal disorder)
HYPO (Congenital Anomalies of the Newborn--Hypospadias)is equivalent to416010008 (Hypospadias)

Source

{
  "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"
            }
          ]
        }
      ]
    }
  ]
}