Birth And Fetal Death (BFDR) FHIR Implementation Guide, published by HL7 International / Public Health. This guide is not an authorized publication; it is the continuous build for version 2.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/fhir-bfdr/ and changes regularly. See the Directory of published versions
{
"resourceType" : "Condition",
"id" : "condition-congenital-anomaly-of-newborn-babyg-quinn-2",
"meta" : {
"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 class=\"res-header-id\"><b>Generated Narrative: Condition condition-congenital-anomaly-of-newborn-babyg-quinn-2</b></p><a name=\"condition-congenital-anomaly-of-newborn-babyg-quinn-2\"> </a><a name=\"hccondition-congenital-anomaly-of-newborn-babyg-quinn-2\"> </a><a name=\"condition-congenital-anomaly-of-newborn-babyg-quinn-2-en-US\"> </a><p><b>clinicalStatus</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/condition-clinical active}\">Active</span></p><p><b>category</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/condition-category problem-list-item}\">Problem List Item</span>, <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)</a></p><h3>Evidences</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Code</b></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{http://snomed.info/sct 312948004}\">Karyotype determination pending</span></td></tr></table></div>"
},
"clinicalStatus" : {
"coding" : [
{
"system" : "http://terminology.hl7.org/CodeSystem/condition-clinical",
"code" : "active",
"display" : "Active"
}
],
"text" : "Active"
},
"category" : [
{
"coding" : [
{
"system" : "http://terminology.hl7.org/CodeSystem/condition-category",
"code" : "problem-list-item",
"display" : "Problem List Item"
}
]
},
{
"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"
}
]
}
]
}