{
  "resourceType" : "DeviceDefinition",
  "id" : "mii-dd-mtb-panel-wgs",
  "meta" : {
    "profile" : ["https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/StructureDefinition/mii-pr-mtb-panel-devicedefinition"]
  },
  "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: DeviceDefinition mii-dd-mtb-panel-wgs</b></p><a name=\"de-mii-dd-mtb-panel-wgs\"> </a><a name=\"de-hcmii-dd-mtb-panel-wgs\"> </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-mtb-panel-devicedefinition.html\">MII PR MTB Panel DeviceDefinition</a></p></div><h3>DeviceNames</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Name</b></td><td><b>Type</b></td></tr><tr><td style=\"display: none\">*</td><td>Whole Genome Sequencing (generisch)</td><td>User Friendly name</td></tr></table><p><b>type</b>: <span title=\"Codes:{https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-genomicanalysis-devicefunction gene-panel}\">Genpanel</span></p><blockquote><p><b>capability</b></p><p><b>type</b>: <span title=\"Codes:{https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-panel-capability snv-detection}\">SNV-Detektion</span></p></blockquote><blockquote><p><b>capability</b></p><p><b>type</b>: <span title=\"Codes:{https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-panel-capability fusion-detection}\">Fusions-Detektion</span></p></blockquote><blockquote><p><b>capability</b></p><p><b>type</b>: <span title=\"Codes:{https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-panel-capability deletion-detection}\">Deletions-Detektion</span></p></blockquote><blockquote><p><b>capability</b></p><p><b>type</b>: <span title=\"Codes:{https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-panel-capability amplification-detection}\">Amplifikations-Detektion</span></p></blockquote><p><b>url</b>: <a href=\"https://simplifier.net/resolve?scope=de.basisprofil.r4@1.6.0&amp;canonical=https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/DeviceDefinition/mii-dd-mtb-panel-wgs\">https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/DeviceDefinition/mii-dd-mtb-panel-wgs</a></p><p><b>note</b>: </p><blockquote><div><p>Genomweite Sequenzierung; keine endliche Panelliste (all_assessed).</p>\n</div></blockquote></div>"
  },
  "deviceName" : [{
    "name" : "Whole Genome Sequencing (generisch)",
    "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"
      }]
    }
  },
  {
    "type" : {
      "coding" : [{
        "system" : "https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-panel-capability",
        "code" : "fusion-detection"
      }]
    }
  },
  {
    "type" : {
      "coding" : [{
        "system" : "https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-panel-capability",
        "code" : "deletion-detection"
      }]
    }
  },
  {
    "type" : {
      "coding" : [{
        "system" : "https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-panel-capability",
        "code" : "amplification-detection"
      }]
    }
  }],
  "url" : "https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/DeviceDefinition/mii-dd-mtb-panel-wgs",
  "note" : [{
    "text" : "Genomweite Sequenzierung; keine endliche Panelliste (all_assessed)."
  }]
}