Birth Defects Reporting - STU1, published by HL7 International / Public Health. This guide is not an authorized publication; it is the continuous build for version 0.1.2 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/fhir-birthdefectsreporting-ig/ and changes regularly. See the Directory of published versions

• Narrative Content
• XML
• JSON
• TTL

: ReportableDiagnosisExample - JSON Representation

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{
  "resourceType" : "Condition",
  "id" : "ReportableDiagnosisExample",
  "meta" : {
    "profile" : [
      🔗 "http://hl7.org/fhir/us/birthdefectreporting/StructureDefinition/bdr-reportablediagnosis"
    ]
  },
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: Condition ReportableDiagnosisExample</b></p><a name=\"ReportableDiagnosisExample\"> </a><a name=\"hcReportableDiagnosisExample\"> </a><a name=\"ReportableDiagnosisExample-en-US\"> </a><p><b>clinicalStatus</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/condition-clinical active}\">Active</span></p><p><b>verificationStatus</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/condition-ver-status confirmed}\">Confirmed</span></p><p><b>category</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/condition-category encounter-diagnosis}\">Encounter Diagnosis</span></p><p><b>code</b>: <span title=\"Codes:{http://snomed.info/sct 719046005}\">12q14 microdeletion syndrome (disorder)</span></p><p><b>subject</b>: <a href=\"Patient-PatientChildExample.html\">Gene Austin Wellington (official) Male, DoB: 2020-04-28 ( Medical record number)</a></p><p><b>onset</b>: 2020-07-15</p><h3>Evidences</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Detail</b></td></tr><tr><td style=\"display: none\">*</td><td><a href=\"Procedure-ConfirmatoryTestExampleWES.html\">Procedure Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis</a></td></tr></table></div>"
  },
  "clinicalStatus" : {
    "coding" : [
      {
        "system" : "http://terminology.hl7.org/CodeSystem/condition-clinical",
        "code" : "active",
        "display" : "Active"
      }
    ]
  },
  "verificationStatus" : {
    "coding" : [
      {
        "system" : "http://terminology.hl7.org/CodeSystem/condition-ver-status",
        "code" : "confirmed",
        "display" : "Confirmed"
      }
    ]
  },
  "category" : [
    {
      "coding" : [
        {
          "system" : "http://terminology.hl7.org/CodeSystem/condition-category",
          "code" : "encounter-diagnosis"
        }
      ]
    }
  ],
  "code" : {
    "coding" : [
      {
        "system" : "http://snomed.info/sct",
        "code" : "719046005",
        "display" : "12q14 microdeletion syndrome (disorder)"
      }
    ]
  },
  "subject" : {
    🔗 "reference" : "Patient/PatientChildExample"
  },
  "onsetDateTime" : "2020-07-15",
  "evidence" : [
    {
      "detail" : [
        {
          🔗 "reference" : "Procedure/ConfirmatoryTestExampleWES"
        }
      ]
    }
  ]
}