臺灣次世代基因定序檢測實作指引
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臺灣次世代基因定序檢測實作指引 - Local Development build (v0.1.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions
{
"resourceType" : "DiagnosticReport",
"id" : "diag-min",
"meta" : {
"profile" : [
🔗 "http://example.org/StructureDefinition/DiagnosticReport-twngs"
]
},
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: DiagnosticReport diag-min</b></p><a name=\"diag-min\"> </a><a name=\"hcdiag-min\"> </a><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\"/><p style=\"margin-bottom: 0px\">Profile: <a href=\"StructureDefinition-DiagnosticReport-twngs.html\">基因定序檢測報告-DiagnosticReport TWNGS</a></p></div><h2><span title=\"Codes:{http://loinc.org 51969-4}\">XX 癌症基因檢測</span> </h2><table class=\"grid\"><tr><td>Subject</td><td>王大明 Male, DoB: 2001-01-01 ( Medical record number\u00a0(use:\u00a0official,\u00a0))</td></tr><tr><td>When For</td><td>2024-05-07</td></tr><tr><td>Performer</td><td> <a href=\"Organization-org-gene-min.html\">Organization XX檢驗實驗室</a></td></tr></table><p><b>Report Details</b></p><table class=\"grid\"><tr><td><b>Code</b></td><td><b>Value</b></td><td><b>Flags</b></td><td><b>Note</b></td><td><b>When For</b></td></tr><tr><td><a href=\"Observation-obs-geneinfo-min.html\"><span title=\"Codes:{http://loinc.org 51969-4}\">Genetic analysis report</span></a></td><td/><td>Final</td><td/><td>2024-01-01</td></tr><tr><td><a href=\"Observation-obs-variant-min.html\"><span title=\"Codes:{http://loinc.org 69548-6}\">Genetic variant assessment</span></a></td><td/><td>Final</td><td/><td>2024-01-01</td></tr><tr><td><a href=\"Observation-obs-fusion-min.html\"><span title=\"Codes:{http://example.org/CodeSystem/genomic-observation-type-cs fusion}\">Fusion</span></a></td><td>EML4::ALK</td><td>Final</td><td/><td>2024-01-01</td></tr><tr><td><a href=\"Observation-obs-cnv-min.html\"><span title=\"Codes:{http://loinc.org 82155-3}\">Genomic structural variant copy number</span></a></td><td>8 copy number</td><td>Final, <span title=\"Codes:{http://example.org/CodeSystem/cnv-interpretation-cs amplification}\">Amplification</span></td><td/><td>2024-01-01</td></tr><tr><td><a href=\"Observation-obs-biomarker-min.html\"><span title=\"Codes:{http://example.org/CodeSystem/genomic-observation-type-cs biomarker}\">Biomarker</span></a></td><td/><td>Final</td><td><blockquote><div><p>HRD (Homologous Recombination Deficiency)-high HLA LOH (Human Leukocyte Antigen Loss of Heterozygosity) -HLA-A loss</p>\n</div></blockquote></td><td>2024-01-01</td></tr><tr><td><a href=\"Observation-obs-othvar-min.html\"><span title=\"Codes:{http://example.org/CodeSystem/genomic-observation-type-cs othVar}\">Other Types of Variant</span></a></td><td>complex rearrangement</td><td>Final</td><td/><td>2024-01-01</td></tr></table></div>"
},
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"url" : "http://example.org/StructureDefinition/extension-DiagnosticReport-condition",
"valueReference" : {
🔗 "reference" : "Condition/con-min"
}
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],
"basedOn" : [
{
🔗 "reference" : "ServiceRequest/serReq-min"
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"status" : "final",
"code" : {
"coding" : [
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"system" : "http://loinc.org",
"code" : "51969-4",
"display" : "Genetic analysis report"
}
],
"text" : "XX 癌症基因檢測"
},
"subject" : {
🔗 "reference" : "Patient/pat-min"
},
"effectiveDateTime" : "2024-05-07",
"performer" : [
{
🔗 "reference" : "Organization/org-gene-min"
}
],
"result" : [
{
🔗 "reference" : "Observation/obs-geneinfo-min"
},
{
🔗 "reference" : "Observation/obs-variant-min"
},
{
🔗 "reference" : "Observation/obs-fusion-min"
},
{
🔗 "reference" : "Observation/obs-cnv-min"
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{
🔗 "reference" : "Observation/obs-biomarker-min"
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{
🔗 "reference" : "Observation/obs-othvar-min"
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]
}