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FHIR IG Statistics: ConceptMap/mii-cm-onko-genetische-variante-auspraegung-sct

Packagede.medizininformatikinitiative.kerndatensatz.onkologie
Resource TypeConceptMap
Idmii-cm-onko-genetische-variante-auspraegung-sct
FHIR VersionR4
Sourcehttps://simplifier.net/resolve?scope=de.medizininformatikinitiative.kerndatensatz.onkologie@2025.1.0&canonical=https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/ConceptMap/mii-cm-onko-genetische-variante-auspraegung-sct
URLhttps://www.medizininformatik-initiative.de/fhir/ext/modul-onko/ConceptMap/mii-cm-onko-genetische-variante-auspraegung-sct
Version2025.1.0
Statusactive
Date2024-04-10
NameMII CM Onko Genetische Variante Auspraegung SCT Mapping
TitleMII CM Onko Genetische Variante Auspraegung SNOMED Mapping
Realmde
DescriptionMapping Therapieabweichung Codes zu SNOMED-CT
PurposeTechnical mapping to transform oBDS-Data into SNOMED

Resources that use this resource

No resources found


Resources that this resource uses

CodeSystem
mii-cs-onko-genetische-variante-auspraegungMII CS Onkologie Genetische Variante Ausprägung

Narrative

No narrative content found in resource


Source

{
  "resourceType": "ConceptMap",
  "id": "mii-cm-onko-genetische-variante-auspraegung-sct",
  "url": "https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/ConceptMap/mii-cm-onko-genetische-variante-auspraegung-sct",
  "version": "2025.1.0",
  "name": "MII CM Onko Genetische Variante Auspraegung SCT Mapping",
  "title": "MII CM Onko Genetische Variante Auspraegung SNOMED Mapping",
  "status": "active",
  "experimental": false,
  "date": "2024-04-10",
  "description": "Mapping Therapieabweichung Codes zu SNOMED-CT",
  "purpose": "Technical mapping to transform oBDS-Data into SNOMED",
  "sourceUri": "https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/",
  "targetUri": "http://snomed.info/sct/900000000000207008/version/20240401",
  "group": [
    {
      "source": "https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/CodeSystem/mii-cs-onko-genetische-variante-auspraegung",
      "target": "http://snomed.info/sct/900000000000207008/version/20240401",
      "element": [
        {
          "code": "M",
          "display": "Mutation/positiv",
          "target": [
            {
              "code": "55446002",
              "display": "Genetic mutation (finding)",
              "equivalence": "equivalent"
            }
          ]
        },
        {
          "code": "W",
          "display": "Wildtyp/nicht mutiert/ negativ",
          "target": [
            {
              "code": "412730000",
              "display": "Genetic finding not detected (finding)",
              "equivalence": "equivalent"
            }
          ]
        },
        {
          "code": "P",
          "display": "Polymorphismus",
          "target": [
            {
              "code": "50334000",
              "display": "Genetic polymorphism (finding)",
              "equivalence": "equivalent"
            }
          ]
        },
        {
          "code": "S",
          "display": "Sonstiges",
          "target": [
            {
              "code": "74964007",
              "display": "Other (qualifier value)",
              "equivalence": "equivalent"
            }
          ]
        },
        {
          "code": "N",
          "display": "Nicht bestimmbar",
          "target": [
            {
              "code": "1156316003",
              "display": "Cannot be determined (qualifier value)",
              "equivalence": "equivalent"
            }
          ]
        },
        {
          "code": "U",
          "display": "Unbekannt",
          "target": [
            {
              "code": "261665006",
              "display": "Unknown (qualifier value)",
              "equivalence": "equivalent"
            }
          ]
        }
      ]
    }
  ]
}