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Resource ConceptMap/FHIR Server from package de.medizininformatikinitiative.kerndatensatz.onkologie#2025.0.3 (94 ms)

Package de.medizininformatikinitiative.kerndatensatz.onkologie
Type ConceptMap
Id Id
FHIR Version R4
Source https://simplifier.net/resolve?scope=de.medizininformatikinitiative.kerndatensatz.onkologie@2025.0.3&canonical=https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/ConceptMap/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
Status active
Date 2024-04-10
Name MII CM Onko Genetische Variante Auspraegung SCT Mapping
Title MII CM Onko Genetische Variante Auspraegung SNOMED Mapping
Experimental False
Realm de
Description Mapping Therapieabweichung Codes zu SNOMED-CT
Purpose Technical mapping to transform oBDS-Data into SNOMED

Resources that use this resource

No resources found


Resources that this resource uses

CodeSystem
http://snomed.info/sct SNOMED CT (all versions)
http://snomed.info/sct SNOMED CT (all versions)
http://snomed.info/sct veri
https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/CodeSystem/mii-cs-onko-genetische-variante-auspraegung MII CS Onkologie Genetische Variante Ausprägung


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",
  "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",
  "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",
          "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"
            }
          ]
        }
      ]
    }
  ],
  "text" : {
  }
}

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