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Packagede.medizininformatikinitiative.kerndatensatz.molgen
Resource TypeBundle
IdBundle-mii-exa-befund-bundle-befund-srcc.json
FHIR VersionR4

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Source1

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  "resourceType": "Bundle",
  "id": "mii-exa-befund-bundle-befund-srcc",
  "type": "transaction",
  "timestamp": "2022-12-16T10:09:00+01:00",
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            "country": "DE"
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      },
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        "url": "Patient/mii-exa-molgen-patient-srcc"
      }
    },
    {
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      "resource": {
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        "id": "mii-exa-molgen-practitioner-lab",
        "active": true,
        "name": [
          {
            "use": "official",
            "text": "Dr. Daniel Schmidt",
            "family": "Schmidt",
            "given": [
              "Daniel"
            ],
            "prefix": [
              "Dr."
            ]
          }
        ]
      },
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    },
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            "prefix": [
              "Dr."
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    },
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        "resourceType": "Specimen",
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          ]
        },
        "subject": {
          "reference": "Patient/mii-exa-molgen-patient-srcc"
        },
        "receivedTime": "2022-11-30",
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      },
      "request": {
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        "url": "Specimen/mii-exa-molgen-specimen-srcc-2"
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    },
    {
      "fullUrl": "https://www.medizininformatik-initiative.de/fhir/mii-exa-molgen-molekulargenetischer-befundbericht-srcc",
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            "reference": "Observation/mii-exa-molgen-diagnostische-implikation-srcc-ctnna1"
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            "reference": "Observation/mii-exa-molgen-variante-srcc-ctnna1"
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              "display": "Molecular genetic test (procedure)"
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          ],
          "text": "Molekulargenetische Untersuchung (Stufendiagnostik) der relevanten Gene"
        },
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          "reference": "Patient/mii-exa-molgen-patient-srcc"
        },
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                "code": "C16.9",
                "display": "Bösartige Neubildung: Magen, nicht näher bezeichnet"
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                "code": "429740004",
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      "fullUrl": "https://www.medizininformatik-initiative.de/fhir/mii-exa-molgen-device-sequencer",
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        "resourceType": "Device",
        "id": "mii-exa-molgen-device-sequencer",
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            "name": "MiSeq",
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      "fullUrl": "https://www.medizininformatik-initiative.de/fhir/mii-exa-molgen-variante-srcc-ctnna1",
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        "resourceType": "Observation",
        "id": "mii-exa-molgen-variante-srcc-ctnna1",
        "meta": {
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      },
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        "method": "PUT",
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    },
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          ]
        },
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        },
        "effectiveDateTime": "2022-11-30",
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              ]
            },
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            "valueCodeableConcept": {
              "coding": [
                {
                  "system": "http://snomed.info/sct",
                  "code": "716859000",
                  "display": "Hereditary diffuse carcinoma of stomach (disorder)"
                }
              ]
            }
          }
        ]
      },
      "request": {
        "method": "PUT",
        "url": "Observation/mii-exa-molgen-diagnostische-implikation-srcc-ctnna1"
      }
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}