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Packageuk.nhsengland.genomics.r4
Resource TypePlanDefinition
IdDGTS-PlanDefinition-Example.json
FHIR VersionR4
Sourcehttps://simplifier.net/resolve?scope=uk.nhsengland.genomics.r4@0.5.2&canonical=http://fhir.nhs.uk/PlanDefinition/TP231
URLhttp://fhir.nhs.uk/PlanDefinition/TP231
Version1.0
Statusactive
TitleAngelman syndrome

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Source1

{
  "resourceType": "PlanDefinition",
  "id": "DGTS-PlanDefinition-Example",
  "url": "http://fhir.nhs.uk/PlanDefinition/TP231",
  "identifier": [
    {
      "system": "https://fhir.nhs.uk/Id/England-DigitalGenomicTestServices",
      "value": "TP231"
    },
    {
      "system": "https://fhir.nhs.uk/Id/England-GenomicTestDirectory",
      "value": "R47",
      "use": "old"
    }
  ],
  "title": "Angelman syndrome",
  "status": "active",
  "experimental": false,
  "version": "1.0",
  "useContext": [
    {
      "code": {
        "code": "user",
        "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
      },
      "valueCodeableConcept": {
        "coding": [
          {
            "code": "400",
            "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-PracticeSettingCode",
            "display": "Neurology"
          }
        ]
      }
    },
    {
      "code": {
        "code": "user",
        "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
      },
      "valueCodeableConcept": {
        "coding": [
          {
            "code": "420",
            "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-PracticeSettingCode",
            "display": "Paediatrics"
          }
        ]
      }
    },
    {
      "code": {
        "code": "user",
        "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
      },
      "valueCodeableConcept": {
        "coding": [
          {
            "code": "311",
            "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-PracticeSettingCode",
            "display": "Clinical Genetics"
          }
        ]
      }
    },
    {
      "code": {
        "code": "focus",
        "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
      },
      "valueCodeableConcept": {
        "coding": [
          {
            "code": "diagnostic",
            "system": "https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics"
          }
        ]
      }
    }
  ],
  "goal": [
    {
      "description": {
        "coding": [
          {
            "code": "rare-disease-non-wgs",
            "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory",
            "display": "Rare Disease - Non-WGS"
          }
        ]
      }
    }
  ],
  "action": [
    {
      "definitionCanonical": "http://fhir.nhs.uk/ActivityDefinition/GT1"
    },
    {
      "definitionCanonical": "http://fhir.nhs.uk/ActivityDefinition/GT36"
    },
    {
      "definitionCanonical": "http://fhir.nhs.uk/ActivityDefinition/GT103"
    },
    {
      "definitionCanonical": "http://fhir.nhs.uk/ActivityDefinition/GT417"
    },
    {
      "definitionCanonical": "http://fhir.nhs.uk/ActivityDefinition/GT732"
    },
    {
      "definitionCanonical": "http://fhir.nhs.uk/ActivityDefinition/GT858"
    },
    {
      "definitionCanonical": "http://fhir.nhs.uk/ActivityDefinition/GT897"
    },
    {
      "definitionCanonical": "http://fhir.nhs.uk/ActivityDefinition/GT1124"
    }
  ]
}