NAPKON Pediatrics Module
1.0.0 - trial-use
NAPKON Pediatrics Module - Local Development build (v1.0.0). See the Directory of published versions
{
"resourceType" : "Condition",
"id" : "CongenitalAtransferrinemiaConfirmed",
"meta" : {
"profile" : [
"https://www.napkon.de/fhir/StructureDefinition/congenital-disease"
]
},
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative</b></p><p><b>verificationStatus</b>: <span title=\"Codes: {http://terminology.hl7.org/CodeSystem/condition-ver-status confirmed}, {http://snomed.info/sct 410605003}\">Confirmed present (qualifier value)</span></p><p><b>category</b>: <span title=\"Codes: {http://snomed.info/sct 394537008}, {http://terminology.hl7.org/CodeSystem/observation-category laboratory}\">Pediatric specialty (qualifier value)</span></p><p><b>code</b>: <span title=\"Codes: {http://snomed.info/sct 111571009}\">Congenital atransferrinemia (disorder)</span></p><p><b>subject</b>: <a href=\"Patient-ExamplePatient.html\">Generated Summary: Medical record number: napkon-example-patient; maxi musterperson (OFFICIAL); gender: unknown; birthDate: 1990-08-08</a></p><p><b>recordedDate</b>: Feb 19, 2021, 8:30:35 AM</p></div>"
},
"verificationStatus" : {
"coding" : [
{
"system" : "http://terminology.hl7.org/CodeSystem/condition-ver-status",
"code" : "confirmed"
},
{
"system" : "http://snomed.info/sct",
"code" : "410605003",
"display" : "Confirmed present (qualifier value)"
}
]
},
"category" : [
{
"coding" : [
{
"system" : "http://snomed.info/sct",
"code" : "394537008",
"display" : "Pediatric specialty (qualifier value)"
},
{
"system" : "http://terminology.hl7.org/CodeSystem/observation-category",
"code" : "laboratory",
"display" : "Laboratory"
}
]
}
],
"code" : {
"coding" : [
{
"system" : "http://snomed.info/sct",
"code" : "111571009",
"display" : "Congenital atransferrinemia (disorder)"
}
]
},
"subject" : {
"reference" : "Patient/ExamplePatient"
},
"recordedDate" : "2021-02-19T09:30:35+01:00"
}