Phenomics Exchange for Research and Diagnostics, published by HL7 International / Clinical Interoperability Council. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/phenomics-exchange-ig/ and changes regularly. See the Directory of published versions
{
"resourceType" : "Condition",
"id" : "vitreoretinochoroidopathy",
"meta" : {
"profile" : [
🔗 "http://hl7.org/fhir/uv/phenomics-exchange/StructureDefinition/Disease"
]
},
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative: Condition </b><a name=\"vitreoretinochoroidopathy\"> </a><a name=\"hcvitreoretinochoroidopathy\"> </a></p><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\">ResourceCondition "vitreoretinochoroidopathy" </p><p style=\"margin-bottom: 0px\">Profile: <a href=\"StructureDefinition-Disease.html\">Disease profile</a></p></div><p><b>clinicalStatus</b>: Active <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (<a href=\"http://terminology.hl7.org/5.5.0/CodeSystem-condition-clinical.html\">Condition Clinical Status Codes</a>#active)</span></p><p><b>code</b>: Autosomal dominant vitreoretinochoroidopathy (disorder) <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (<a href=\"https://browser.ihtsdotools.org/\">SNOMED CT</a>#711162004)</span></p><p><b>subject</b>: <a href=\"Patient-example-patient.html\">Patient/example-patient</a> " ANYPERSON"</p></div>"
},
"clinicalStatus" : {
"coding" : [
{
"system" : "http://terminology.hl7.org/CodeSystem/condition-clinical",
"code" : "active",
"display" : "Active"
}
]
},
"code" : {
"coding" : [
{
"system" : "http://snomed.info/sct",
"code" : "711162004",
"display" : "Autosomal dominant vitreoretinochoroidopathy (disorder)"
}
]
},
"subject" : {
🔗 "reference" : "Patient/example-patient"
}
}