MII IG Kerndatensatz-Modul Seltene Erkrankungen
2027.0.0-ballot - Germany

This page is part of the MII Implementation Guide Seltene Erkrankungen (v2027.0.0-ballot: 2027 Ballot 1) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions

: Beispiel Genetische Beratung

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{
  "resourceType" : "ServiceRequest",
  "id" : "mii-exa-seltene-therapieempfehlung-genetische-beratung",
  "meta" : {
    "profile" : [
      🔗 "https://www.medizininformatik-initiative.de/fhir/ext/modul-seltene/StructureDefinition/mii-pr-seltene-therapieempfehlung-nicht-medikamentoes|2027.0.0-ballot"
    ]
  },
  "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: ServiceRequest mii-exa-seltene-therapieempfehlung-genetische-beratung</b></p><a name=\"de-mii-exa-seltene-therapieempfehlung-genetische-beratung\"> </a><a name=\"de-hcmii-exa-seltene-therapieempfehlung-genetische-beratung\"> </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-seltene-therapieempfehlung-nicht-medikamentoes.html\">MII PR SE Therapieempfehlung Nicht-Medikamentös</a> version: 2027.0.0-ballot</p></div><p><b>status</b>: Active</p><p><b>intent</b>: Proposal</p><p><b>category</b>: <span title=\"Codes:{https://www.medizininformatik-initiative.de/fhir/ext/modul-seltene/CodeSystem/mii-cs-seltene-therapieempfehlung-strategie other}\">Sonstige</span>, <span title=\"Codes:{https://www.medizininformatik-initiative.de/fhir/ext/modul-seltene/CodeSystem/mii-cs-seltene-therapieempfehlung-typ symptomatic}\">Symptomatisch</span></p><p><b>priority</b>: Routine</p><p><b>code</b>: <span title=\"Codes:{http://snomed.info/sct 409063005}\">Humangenetische Beratung</span></p><p><b>subject</b>: <a href=\"Patient-mii-exa-seltene-patient.html\">Max Mustermann (official) Male, DoB: 1990-01-01 ( http://test-krankenhaus.de/fhir/sid/patienten#12345)</a></p><p><b>authoredOn</b>: 2024-11-01</p><p><b>reasonCode</b>: <span title=\"Codes:{http://snomed.info/sct 429962007}\">Family history of hereditary disease</span></p><p><b>note</b>: </p><blockquote><div><p>Beratung bezüglich Vererbungsmodus und Wiederholungsrisiko</p>\n</div></blockquote></div>"
  },
  "status" : "active",
  "intent" : "proposal",
  "category" : [
    {
      "coding" : [
        {
          "system" : "https://www.medizininformatik-initiative.de/fhir/ext/modul-seltene/CodeSystem/mii-cs-seltene-therapieempfehlung-strategie",
          "code" : "other",
          "display" : "Sonstige"
        }
      ]
    },
    {
      "coding" : [
        {
          "system" : "https://www.medizininformatik-initiative.de/fhir/ext/modul-seltene/CodeSystem/mii-cs-seltene-therapieempfehlung-typ",
          "code" : "symptomatic",
          "display" : "Symptomatisch"
        }
      ]
    }
  ],
  "priority" : "routine",
  "code" : {
    "coding" : [
      {
        "system" : "http://snomed.info/sct",
        "code" : "409063005",
        "display" : "Counseling"
      }
    ],
    "text" : "Humangenetische Beratung"
  },
  "subject" : {
    🔗 "reference" : "Patient/mii-exa-seltene-patient"
  },
  "authoredOn" : "2024-11-01",
  "reasonCode" : [
    {
      "coding" : [
        {
          "system" : "http://snomed.info/sct",
          "code" : "429962007",
          "display" : "Family history of hereditary disease"
        }
      ]
    }
  ],
  "note" : [
    {
      "text" : "Beratung bezüglich Vererbungsmodus und Wiederholungsrisiko"
    }
  ]
}