PanCareSurPass Project HL7 FHIR Implementation Guide, published by PanCareSurPass Project. This guide is not an authorized publication; it is the continuous build for version 0.2.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-eu/pcsp/ and changes regularly. See the Directory of published versions
{
"resourceType" : "Condition",
"id" : "ConditionPrimCancerMainzZeisig",
"meta" : {
"profile" : [
🔗 "http://hl7.eu/fhir/ig/pcsp/StructureDefinition/Condition-primaryCancer-eu-pcsp"
]
},
"text" : {
"status" : "extensions",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: Condition ConditionPrimCancerMainzZeisig</b></p><a name=\"ConditionPrimCancerMainzZeisig\"> </a><a name=\"hcConditionPrimCancerMainzZeisig\"> </a><a name=\"ConditionPrimCancerMainzZeisig-en-US\"> </a><p><b>Condition Asserted Date</b>: 2007-04-04</p><p><b>Histology-Morphology-Behavior Extension</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/icd-o-3 91813}\">91813</span></p><p><b>code</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/iccc-3 081}\">081</span></p><p><b>bodySite</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/icd-o-3 C401}\">C401</span></p><p><b>subject</b>: <a href=\"Patient-PatientMainzZeisig.html\">Sarah Zeisig Female, DoB: 1996-12-12 ( http://hl7.eu/fhir/ig/pcsp/sid/pat-id-mainz#L0010)</a></p><p><b>encounter</b>: <a href=\"Encounter-EncounterPrimCancerMainzZeisig.html\">Encounter: status = finished; class = ambulatory (ActCode#AMB); period = 2007-07-07 --> (ongoing)</a></p><h3>Stages</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Summary</b></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:\">textual description of stage</span></td></tr></table><blockquote><p><b>evidence</b></p><p><b>detail</b>: <a href=\"Observation-ObservationPrimCancerMainzZeisig.html\">Observation Diagnosis</a></p></blockquote><blockquote><p><b>evidence</b></p><p><b>code</b>: <span title=\"Codes:{http://snomed.info/sct 106221001}\">Textual description of Genetic markers</span></p></blockquote><blockquote><p><b>evidence</b></p><p><b>code</b>: <span title=\"Codes:{http://snomed.info/sct 365861007}\">Textual description of Immunology</span></p></blockquote><blockquote><p><b>evidence</b></p><p><b>code</b>: <span title=\"Codes:{http://snomed.info/sct 32895009}\">Textual description of hereditary predisposition</span></p></blockquote></div>"
},
"extension" : [
{
"url" : "http://hl7.org/fhir/StructureDefinition/condition-assertedDate",
"valueDateTime" : "2007-04-04"
},
{
"url" : "http://hl7.org/fhir/us/mcode/StructureDefinition/mcode-histology-morphology-behavior",
"valueCodeableConcept" : {
"coding" : [
{
"system" : "http://terminology.hl7.org/CodeSystem/icd-o-3",
"code" : "91813"
}
]
}
}
],
"code" : {
"coding" : [
{
"system" : "http://terminology.hl7.org/CodeSystem/iccc-3",
"code" : "081"
}
]
},
"bodySite" : [
{
"extension" : [
{
"url" : "http://hl7.eu/fhir/ig/pcsp/StructureDefinition/mcode-laterality-qualifier",
"valueCodeableConcept" : {
"coding" : [
{
"system" : "http://loinc.org",
"code" : "LA4585-1",
"display" : "Left"
}
]
}
}
],
"coding" : [
{
"system" : "http://terminology.hl7.org/CodeSystem/icd-o-3",
"code" : "C401"
}
]
}
],
"subject" : {
🔗 "reference" : "Patient/PatientMainzZeisig"
},
"encounter" : {
🔗 "reference" : "Encounter/EncounterPrimCancerMainzZeisig"
},
"stage" : [
{
"summary" : {
"text" : "textual description of stage"
}
}
],
"evidence" : [
{
"detail" : [
{
🔗 "reference" : "Observation/ObservationPrimCancerMainzZeisig"
}
]
},
{
"code" : [
{
"coding" : [
{
"system" : "http://snomed.info/sct",
"code" : "106221001",
"display" : "Genetic finding"
}
],
"text" : "Textual description of Genetic markers"
}
]
},
{
"code" : [
{
"coding" : [
{
"system" : "http://snomed.info/sct",
"code" : "365861007",
"display" : "Finding of immune status"
}
],
"text" : "Textual description of Immunology"
}
]
},
{
"code" : [
{
"coding" : [
{
"system" : "http://snomed.info/sct",
"code" : "32895009",
"display" : "Hereditary disease"
}
],
"text" : "Textual description of hereditary predisposition"
}
]
}
]
}