FHIR IG analytics

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Narrative

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Source1

{
  "resourceType": "DeviceDefinition",
  "id": "mii-dd-mtb-panel-cgp",
  "meta": {
    "profile": [
      "https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/StructureDefinition/mii-pr-mtb-panel-devicedefinition"
    ]
  },
  "text": {
    "status": "extensions",
    "div": "<!-- snip (see above) -->"
  },
  "extension": [
    {
      "extension": [
        {
          "url": "geneList",
          "valueCanonical": "https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/ValueSet/mii-vs-mtb-panel-cgp"
        },
        {
          "url": "scope",
          "valueCodeableConcept": {
            "coding": [
              {
                "system": "https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-panel-capability",
                "code": "snv-detection"
              }
            ]
          }
        }
      ],
      "url": "https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/StructureDefinition/mii-ex-mtb-panel-gene-list"
    }
  ],
  "manufacturerString": "Agilent Technologies",
  "deviceName": [
    {
      "name": "SureSelect Cancer CGP Assay",
      "type": "user-friendly-name"
    }
  ],
  "type": {
    "coding": [
      {
        "system": "https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-genomicanalysis-devicefunction",
        "code": "gene-panel"
      }
    ]
  },
  "capability": [
    {
      "type": {
        "coding": [
          {
            "system": "https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-panel-capability",
            "code": "snv-detection"
          }
        ]
      }
    }
  ],
  "url": "https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/DeviceDefinition/mii-dd-mtb-panel-cgp",
  "onlineInformation": "https://pathologie-ccm.charite.de/fileadmin/user_upload/microsites/m_cc05/pathologie-ccm/00_formulare_documente/00_molekularpathologie/Anlage_Genlisten_NGS-Panel.pdf",
  "note": [
    {
      "text": "602 Gene; nur SNVs."
    }
  ]
}