This page is part of the MII IG Kerndatensatz-Modul Molekulargenetischer Befundbericht (v2027.0.0-ballot.1: Release) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions

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: Polygener Risiko Score BRCA1 Variante

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{
  "resourceType" : "RiskAssessment",
  "id" : "mii-exa-molgen-prs-brca1",
  "meta" : {
    "profile" : [
      🔗 "https://www.medizininformatik-initiative.de/fhir/ext/modul-molgen/StructureDefinition/polygener-risiko-score|2027.0.0-ballot.1"
    ]
  },
  "language" : "de",
  "text" : {
    "status" : "generated",
    "div" : "<div xml:lang=\"de\" lang=\"de\"><hr/><p><b>German</b></p><hr/><p class=\"res-header-id\"><b>Generated Narrative: RiskAssessment mii-exa-molgen-prs-brca1</b></p><a name=\"de-mii-exa-molgen-prs-brca1\"> </a><a name=\"de-hcmii-exa-molgen-prs-brca1\"> </a><div style=\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"><p style=\"margin-bottom: 0px\"/><p style=\"margin-bottom: 0px\">Profile: <a href=\"StructureDefinition-mii-pr-molgen-polygener-risiko-score.html\">MII PR MolGen Polygener Risiko Score</a> version: 2027.0.0-ballot.1</p></div><p><b>status</b>: Final</p><p><b>subject</b>: <a href=\"Patient-mii-exa-molgen-patient-2.html\">Melanie Marie Müller (official) Female, DoB: 2021-09-19 ( Krankenaktennummer\u00a0(use:\u00a0usual,\u00a0))</a></p><p><b>occurrence</b>: 2022-11-01</p><p><b>basis</b>: <a href=\"Observation-mii-exa-molgen-variante-brca1.html\">Observation Genetic variant assessment</a></p><h3>Predictions</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Extension</b></td><td><b>Outcome</b></td><td><b>QualitativeRisk</b></td></tr><tr><td style=\"display: none\">*</td><td/><td><span title=\"Codes:{http://snomed.info/sct 718220008}\">Hereditary breast and ovarian cancer syndrome (disorder)</span></td><td><span title=\"Codes:{http://terminology.hl7.org/CodeSystem/risk-probability high}\">High likelihood</span></td></tr></table></div>"
  },
  "status" : "final",
  "subject" : {
    🔗 "reference" : "Patient/mii-exa-molgen-patient-2"
  },
  "occurrenceDateTime" : "2022-11-01",
  "basis" : [
    {
      🔗 "reference" : "Observation/mii-exa-molgen-variante-brca1"
    }
  ],
  "prediction" : [
    {
      "extension" : [
        {
          "url" : "https://www.medizininformatik-initiative.de/fhir/ext/modul-molgen/StructureDefinition/risk-assessment-einflussfaktor",
          "valueCodeableConcept" : {
            "coding" : [
              {
                "system" : "http://snomed.info/sct",
                "code" : "414152003",
                "display" : "European (ethnic group)"
              }
            ],
            "text" : "Der verwendete Polygene Risikoscore wurde bisher nur für die europäische Bevölkerung bei Brustkrebs validiert."
          }
        }
      ],
      "outcome" : {
        "coding" : [
          {
            "system" : "http://snomed.info/sct",
            "code" : "718220008",
            "display" : "Hereditary breast and ovarian cancer syndrome (disorder)"
          }
        ]
      },
      "qualitativeRisk" : {
        "coding" : [
          {
            "system" : "http://terminology.hl7.org/CodeSystem/risk-probability",
            "code" : "high",
            "display" : "High likelihood"
          }
        ]
      }
    }
  ]
}