GenomeX Data Exchange FHIR IG, published by MITRE. This guide is not an authorized publication; it is the continuous build for version 0.2.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/CodeX-HL7-FHIR-Accelerator/GenomeX-DataExchange/ and changes regularly. See the Directory of published versions

• Narrative Content
• XML
• JSON

: PrenatalResidualRiskPrimaryHyperoxaluriaPatientFemale - JSON Representation

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{
  "resourceType" : "RiskAssessment",
  "id" : "PrenatalResidualRiskPrimaryHyperoxaluriaPatientFemale",
  "meta" : {
    "versionId" : "1",
    "lastUpdated" : "2024-10-02T03:41:34.767+00:00",
    "source" : "#JVN7S7CW0og8nwN0"
  },
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: RiskAssessment PrenatalResidualRiskPrimaryHyperoxaluriaPatientFemale</b></p><a name=\"PrenatalResidualRiskPrimaryHyperoxaluriaPatientFemale\"> </a><a name=\"hcPrenatalResidualRiskPrimaryHyperoxaluriaPatientFemale\"> </a><a name=\"PrenatalResidualRiskPrimaryHyperoxaluriaPatientFemale-en-US\"> </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\">version: 1; Last updated: 2024-10-02 03:41:34+0000; </p><p style=\"margin-bottom: 0px\">Information Source: #JVN7S7CW0og8nwN0</p></div><p><b>status</b>: Final</p><p><b>subject</b>: <a href=\"Patient-PatientFemale.html\">Jenny M (official) Female, DoB: 1988-02-12 ( Patient ID: 7fb905f171204b94b8ee33d33cb624e6\u00a0(use:\u00a0official,\u00a0))</a></p><p><b>occurrence</b>: 2024-06-26</p><p><b>basis</b>: <a href=\"Observation-PrenatalVariantPrimaryHyperoxaluriaPatientFemale.html\">Observation Genetic variant assessment</a></p><h3>Predictions</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Outcome</b></td><td><b>Probability[x]</b></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:\">Patient has a disease-causing mutation for primary hyperoxaluria type 1</span></td><td>0.000057899661704325044</td></tr></table></div>"
  },
  "status" : "final",
  "subject" : {
    🔗 "reference" : "Patient/PatientFemale"
  },
  "occurrenceDateTime" : "2024-06-26",
  "basis" : [
    {
      🔗 "reference" : "Observation/PrenatalVariantPrimaryHyperoxaluriaPatientFemale"
    }
  ],
  "prediction" : [
    {
      "outcome" : {
        "text" : "Patient has a disease-causing mutation for primary hyperoxaluria type 1"
      },
      "probabilityDecimal" : 0.000057899661704325044
    }
  ]
}