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Source1

{
  "resourceType": "ConceptMap",
  "id": "mii-cm-onko-genetische-variante-auspraegung-sct",
  "meta": {
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        "url": "http://hl7.org/fhir/uv/crmi/StructureDefinition/crmi-license",
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      },
      {
        "extension": [
          {
            "url": "packageId",
            "valueId": "de.medizininformatikinitiative.kerndatensatz.onkologie"
          },
          {
            "url": "version",
            "valueString": "2027.0.0-ballot.1"
          },
          {
            "url": "uri",
            "valueUri": "https://www.medizininformatik-initiative.de/fhir/ext/modul-onko"
          }
        ],
        "url": "http://hl7.org/fhir/StructureDefinition/package-source"
      }
    ],
    "profile": [
      "http://hl7.org/fhir/uv/crmi/StructureDefinition/crmi-shareableconceptmap",
      "http://hl7.org/fhir/uv/crmi/StructureDefinition/crmi-publishableconceptmap"
    ]
  },
  "text": {
    "status": "generated",
    "div": "<!-- snip (see above) -->"
  },
  "extension": [
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      "url": "http://hl7.org/fhir/StructureDefinition/cqf-knowledgeCapability",
      "valueCode": "shareable"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/cqf-knowledgeCapability",
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      "valueCodeableConcept": {
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            "display": "Package"
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    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/resource-approvalDate",
      "valueDate": "2026-09-15"
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      "valueContactDetail": {
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            "value": "thomas.debertshaeuser@charite.de"
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      "valueContactDetail": {
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    },
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        "name": "Interoperability Working Group",
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          }
        ]
      }
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/artifact-reviewer",
      "valueContactDetail": {
        "name": "National Steering Committee",
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          }
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    {
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      "valuePeriod": {
        "start": "2027"
      }
    }
  ],
  "url": "https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/ConceptMap/mii-cm-onko-genetische-variante-auspraegung-sct",
  "version": "2027.0.0-ballot.1",
  "name": "MII CM Onko Genetische Variante Auspraegung SCT Mapping",
  "title": "MII CM Onko Genetische Variante Auspraegung SNOMED Mapping",
  "status": "active",
  "experimental": true,
  "date": "2024-04-10",
  "publisher": "Medizininformatik Initiative",
  "contact": [
    {
      "name": "Medizininformatik Initiative",
      "telecom": [
        {
          "system": "url",
          "value": "https://www.medizininformatik-initiative.de/"
        }
      ]
    }
  ],
  "description": "Mapping Therapieabweichung Codes zu SNOMED-CT STATUS DIESER ZUORDNUNG: 2024 erstellt, gegen SNOMED CT International 20240401. Sie ist WEDER OFFIZIELL ENDORSED NOCH FINAL QUALITAETSGESICHERT - es handelt sich um einen projektseitigen Arbeitsstand, nicht um eine abgestimmte Referenz. Die Zielcodes sind gegen neuere SNOMED-Releases nicht nachverifiziert; einzelne Konzepte koennen inzwischen inaktiviert oder ersetzt sein. Vor einer Nutzung in Produktivsystemen sind fachliche Pruefung und ein Abgleich gegen die eingesetzte SNOMED-Version erforderlich.",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "urn:iso:std:iso:3166",
          "code": "DE",
          "display": "Germany"
        }
      ]
    }
  ],
  "purpose": "Technical mapping to transform oBDS-Data into SNOMED",
  "copyright": "This material includes SNOMED Clinical Terms® (SNOMED CT®) which is used by permission of SNOMED International. All rights reserved. SNOMED CT®, was originally created by The College of American Pathologists. SNOMED and SNOMED CT are registered trademarks of SNOMED International. Implementers of these artefacts must have the appropriate SNOMED CT Affiliate license.",
  "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"
            }
          ]
        }
      ]
    }
  ]
}