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Source1

{
  "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|2026.0.1"
    ]
  },
  "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/example"
  },
  "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"
    }
  ]
}