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Packagede.medizininformatikinitiative.kerndatensatz.molgen
Resource TypeServiceRequest
IdServiceRequest-mii-exa-molgen-anforderung-wes.json
FHIR VersionR4

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Narrative

Note: links and images are rebased to the (stated) source


English


Generated Narrative: ServiceRequest mii-exa-molgen-anforderung-wes

Profile: MII PR MolGen Anforderung genetischer Test version: 2027.0.0-ballot.1

status: Completed

intent: Order

code: Whole exome sequence analysis in Blood or Tissue by Molecular genetics method

subject: Maja Julia Van-der-Dussen (official) Female, DoB: 1968-09-19 ( Medical record number (use: usual, ))

authoredOn: 2024-01-10

requester: Practitioner Klaus Müller

reasonCode: Unklare Entwicklungsverzögerung mit Dysmorphiezeichen, V.a. genetisches Syndrom nach unauffälliger Chromosomenanalyse und Array-CGH


German


Generated Narrative: ServiceRequest mii-exa-molgen-anforderung-wes

Profile: MII PR MolGen Anforderung genetischer Test version: 2027.0.0-ballot.1

status: Completed

intent: Order

code: Whole exome sequence analysis in Blood or Tissue by Molecular genetics method

subject: Maja Julia Van-der-Dussen (official) Female, DoB: 1968-09-19 ( Krankenaktennummer (use: usual, ))

authoredOn: 2024-01-10

requester: Practitioner Klaus Müller

reasonCode: Unklare Entwicklungsverzögerung mit Dysmorphiezeichen, V.a. genetisches Syndrom nach unauffälliger Chromosomenanalyse und Array-CGH


Source1

{
  "resourceType": "ServiceRequest",
  "id": "mii-exa-molgen-anforderung-wes",
  "meta": {
    "profile": [
      "https://www.medizininformatik-initiative.de/fhir/ext/modul-molgen/StructureDefinition/anforderung-genetischer-test|2027.0.0-ballot.1"
    ]
  },
  "text": {
    "status": "generated",
    "div": "<!-- snip (see above) -->"
  },
  "status": "completed",
  "intent": "order",
  "code": {
    "coding": [
      {
        "system": "http://loinc.org",
        "code": "86205-2",
        "display": "Whole exome sequence analysis in Blood or Tissue by Molecular genetics method"
      }
    ]
  },
  "subject": {
    "reference": "Patient/mii-exa-molgen-patient"
  },
  "authoredOn": "2024-01-10",
  "requester": {
    "reference": "Practitioner/mii-exa-molgen-practitioner-ordering"
  },
  "reasonCode": [
    {
      "coding": [
        {
          "system": "http://snomed.info/sct",
          "code": "224958001",
          "display": "Global developmental delay"
        }
      ],
      "text": "Unklare Entwicklungsverzögerung mit Dysmorphiezeichen, V.a. genetisches Syndrom nach unauffälliger Chromosomenanalyse und Array-CGH"
    }
  ]
}