{
  "description": "Mapping Therapieabweichung Codes zu SNOMED-CT",
  "_filename": "ConceptMap-mii-cm-onko-genetische-variante-auspraegung-sct.json",
  "package_name": "de.medizininformatikinitiative.kerndatensatz.onkologie",
  "date": "2024-04-10",
  "targetUri": "http://snomed.info/sct",
  "group": [ {
    "source": "https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/CodeSystem/mii-cs-onko-genetische-variante-auspraegung",
    "target": "http://snomed.info/sct",
    "element": [ {
      "code": "M",
      "target": [ {
        "code": "55446002",
        "display": "Genetic mutation (finding)",
        "equivalence": "equivalent"
      } ],
      "display": "Mutation/positiv"
    }, {
      "code": "W",
      "target": [ {
        "code": "412730000",
        "display": "Genetic finding not detected (finding)",
        "equivalence": "equivalent"
      } ],
      "display": "Wildtyp/nicht mutiert/ negativ"
    }, {
      "code": "P",
      "target": [ {
        "code": "50334000",
        "display": "Genetic polymorphism (finding)",
        "equivalence": "equivalent"
      } ],
      "display": "Polymorphismus"
    }, {
      "code": "S",
      "target": [ {
        "code": "74964007",
        "display": "Other (qualifier value)",
        "equivalence": "equivalent"
      } ],
      "display": "Sonstiges"
    }, {
      "code": "N",
      "target": [ {
        "code": "1156316003",
        "display": "Cannot be determined (qualifier value)",
        "equivalence": "equivalent"
      } ],
      "display": "Nicht bestimmbar"
    }, {
      "code": "U",
      "target": [ {
        "code": "261665006",
        "display": "Unknown (qualifier value)",
        "equivalence": "equivalent"
      } ],
      "display": "Unbekannt"
    } ]
  } ],
  "publisher": null,
  "purpose": "Technical mapping to transform oBDS-Data into SNOMED",
  "name": "MII CM Onko Genetische Variante Auspraegung SCT Mapping",
  "type": null,
  "experimental": "false",
  "resourceType": "ConceptMap",
  "title": "MII CM Onko Genetische Variante Auspraegung SNOMED Mapping",
  "package_version": "2025.1.0-alpha",
  "status": "active",
  "id": "b3a32090-6902-4348-a481-9c00a1e5a9d7",
  "kind": null,
  "sourceUri": "https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/",
  "url": "https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/ConceptMap/mii-cm-onko-genetische-variante-auspraegung-sct",
  "version": null
}