Vital Records Birth and Fetal Death Reporting
1.0.0 - STU 1

This page is part of the Vital Records Birth and Fetal Death Reporting (v1.0.0: STU 1 on FHIR R4) based on FHIR R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions

: Condition - Congenital Anomaly of Newborn example [Baby G Quinn] - JSON Representation

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{
  "resourceType" : "Condition",
  "id" : "condition-congenital-anomaly-of-newborn-babyg-quinn-2",
  "meta" : {
    "versionId" : "2",
    "lastUpdated" : "2020-08-20T23:20:37.897+00:00",
    "source" : "#8nHKxfsyONG1qyLw",
    "profile" : [
      "http://hl7.org/fhir/us/bfdr/StructureDefinition/Condition-congenital-anomaly-of-newborn"
    ]
  },
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative</b></p><p><b>category</b>: <span title=\"Codes: {http://loinc.org 73780-9}\">Congenital anomalies of the newborn [US Standard Certificate of Live Birth]</span></p><p><b>code</b>: <span title=\"Codes: {http://snomed.info/sct 70156005}\">Anomaly of chromosome pair 21 (disorder)</span></p><p><b>subject</b>: <a href=\"Patient-patient-child-babyg-quinn.html\">Patient - Child (Baby G Quinn). Generated Summary: Medical Record Number: 9932702 (USUAL); Baby G Quinn ; gender: female; birthDate: 2019-02-12; 1</a></p><h3>Evidences</h3><table class=\"grid\"><tr><td>-</td><td><b>Code</b></td></tr><tr><td>*</td><td><span title=\"Codes: {http://snomed.info/sct 312948004}\">Karyotype determination pending</span></td></tr></table></div>"
  },
  "category" : [
    {
      "coding" : [
        {
          "system" : "http://loinc.org",
          "code" : "73780-9",
          "display" : "Congenital anomalies of the newborn [US Standard Certificate of Live Birth]"
        }
      ]
    }
  ],
  "code" : {
    "coding" : [
      {
        "system" : "http://snomed.info/sct",
        "code" : "70156005",
        "display" : "Anomaly of chromosome pair 21 (disorder)"
      }
    ],
    "text" : "Anomaly of chromosome pair 21 (disorder)"
  },
  "subject" : {
    "reference" : "Patient/patient-child-babyg-quinn",
    "display" : "Patient - Child (Baby G Quinn)"
  },
  "evidence" : [
    {
      "code" : [
        {
          "coding" : [
            {
              "system" : "http://snomed.info/sct",
              "code" : "312948004",
              "display" : "Karyotype determination"
            }
          ],
          "text" : "Karyotype determination pending"
        }
      ]
    }
  ]
}