台灣癌症登記長表實作指引 (Taiwan Cancer Registry Long Form Implementation Guide)
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台灣癌症登記長表實作指引 (Taiwan Cancer Registry Long Form Implementation Guide) - Local Development build (v0.1.1) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions

: SSF1 白血病-白血病染色體檢查的評估代碼系統 - TTL Representation

Active as of 2024-08-01

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@prefix fhir: <http://hl7.org/fhir/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

# - resource -------------------------------------------------------------------

 a fhir:CodeSystem ;
  fhir:nodeRole fhir:treeRoot ;
  fhir:id [ fhir:v "ssf-1-leukemia-codesystem"] ; # 
  fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: CodeSystem ssf-1-leukemia-codesystem</b></p><a name=\"ssf-1-leukemia-codesystem\"> </a><a name=\"hcssf-1-leukemia-codesystem\"> </a><a name=\"ssf-1-leukemia-codesystem-en-US\"> </a><p>This case-sensitive code system <code>https://hapi.fhir.tw/fhir/CodeSystem/ssf-1-leukemia-codesystem</code> defines the following codes:</p><table class=\"codes\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td style=\"white-space:nowrap\">000<a name=\"ssf-1-leukemia-codesystem-000\"> </a></td><td>正常</td></tr><tr><td style=\"white-space:nowrap\">001<a name=\"ssf-1-leukemia-codesystem-001\"> </a></td><td>AML with t(8;21)(q22;q22.1</td></tr><tr><td style=\"white-space:nowrap\">002<a name=\"ssf-1-leukemia-codesystem-002\"> </a></td><td>AML with inv(16)(p13.1q22) or t(16;16)(p13.1;q22)</td></tr><tr><td style=\"white-space:nowrap\">003<a name=\"ssf-1-leukemia-codesystem-003\"> </a></td><td>Acute promyelocytic leukemia with t(15;17)</td></tr><tr><td style=\"white-space:nowrap\">004<a name=\"ssf-1-leukemia-codesystem-004\"> </a></td><td>AML with t(9;11)(p21.3;q23.3)</td></tr><tr><td style=\"white-space:nowrap\">005<a name=\"ssf-1-leukemia-codesystem-005\"> </a></td><td>AML with t(6;9)(p23;q34.1)</td></tr><tr><td style=\"white-space:nowrap\">006<a name=\"ssf-1-leukemia-codesystem-006\"> </a></td><td>AML with inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2)</td></tr><tr><td style=\"white-space:nowrap\">007<a name=\"ssf-1-leukemia-codesystem-007\"> </a></td><td>AML (megakaryoblastic) with t(1;22)(p13.3;q13.1)</td></tr><tr><td style=\"white-space:nowrap\">013<a name=\"ssf-1-leukemia-codesystem-013\"> </a></td><td>AML with t(9;22)(q34;q11)</td></tr><tr><td style=\"white-space:nowrap\">021<a name=\"ssf-1-leukemia-codesystem-021\"> </a></td><td>B lymphoblastic leukemia / lymphoma with t(9;22)(q34.1;q11.2)</td></tr><tr><td style=\"white-space:nowrap\">022<a name=\"ssf-1-leukemia-codesystem-022\"> </a></td><td>B lymphoblastic leukemia / lymphoma with t(v;11q23.3)</td></tr><tr><td style=\"white-space:nowrap\">023<a name=\"ssf-1-leukemia-codesystem-023\"> </a></td><td>B lymphoblastic leukemia / lymphoma with t(12;21)(p13.2;q22.1)</td></tr><tr><td style=\"white-space:nowrap\">024<a name=\"ssf-1-leukemia-codesystem-024\"> </a></td><td>B lymphoblastic leukemia / lymphoma with hyperdiploidy</td></tr><tr><td style=\"white-space:nowrap\">025<a name=\"ssf-1-leukemia-codesystem-025\"> </a></td><td>B lymphoblastic leukemia / lymphoma with hypodiploidy (hypodiploid ALL)</td></tr><tr><td style=\"white-space:nowrap\">026<a name=\"ssf-1-leukemia-codesystem-026\"> </a></td><td>B lymphoblastic leukemia / lymphoma with t(5;14)(q31.1;q32.1)</td></tr><tr><td style=\"white-space:nowrap\">027<a name=\"ssf-1-leukemia-codesystem-027\"> </a></td><td>B lymphoblastic leukemia / lymphoma with t(1;19)(q23;p13.3)</td></tr><tr><td style=\"white-space:nowrap\">041<a name=\"ssf-1-leukemia-codesystem-041\"> </a></td><td>Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)</td></tr><tr><td style=\"white-space:nowrap\">042<a name=\"ssf-1-leukemia-codesystem-042\"> </a></td><td>Mixed phenotype acute leukemia with t(v;11q23.3)</td></tr><tr><td style=\"white-space:nowrap\">051<a name=\"ssf-1-leukemia-codesystem-051\"> </a></td><td>Chronic myelogenous leukemia，t(9;22)</td></tr><tr><td style=\"white-space:nowrap\">061<a name=\"ssf-1-leukemia-codesystem-061\"> </a></td><td>Myelodysplastic syndrome associated with isolated del(5q-)</td></tr><tr><td style=\"white-space:nowrap\">090<a name=\"ssf-1-leukemia-codesystem-090\"> </a></td><td>(1) 一種異常，其他上述未列之染色體異常 (2) 二種異常，其中一種非上述之染色體異常 (3) 二種異常，二種皆非上述之染色體異常</td></tr><tr><td style=\"white-space:nowrap\">091<a name=\"ssf-1-leukemia-codesystem-091\"> </a></td><td>同時有兩種上述之染色體異常</td></tr><tr><td style=\"white-space:nowrap\">092<a name=\"ssf-1-leukemia-codesystem-092\"> </a></td><td>複雜之染色體異常，指三項(含)以上的染色體變化者</td></tr><tr><td style=\"white-space:nowrap\">8XX<a name=\"ssf-1-leukemia-codesystem-8XX\"> </a></td><td>Chromosome study after chemotherapy or immunotherapy or target therapy</td></tr><tr><td style=\"white-space:nowrap\">988<a name=\"ssf-1-leukemia-codesystem-988\"> </a></td><td>不適用。(1) ICD-O-3 M-9811-9837 (EXCEPT C42.0, 42.1, 42.4)</td></tr><tr><td style=\"white-space:nowrap\">998<a name=\"ssf-1-leukemia-codesystem-998\"> </a></td><td>有執行染色體檢查，但結果無法判斷</td></tr><tr><td style=\"white-space:nowrap\">999<a name=\"ssf-1-leukemia-codesystem-999\"> </a></td><td>病歷未記載或不詳或未執行染色體檢查</td></tr></table></div>"
  ] ; # 
  fhir:url [ fhir:v "https://hapi.fhir.tw/fhir/CodeSystem/ssf-1-leukemia-codesystem"^^xsd:anyURI] ; # 
  fhir:version [ fhir:v "0.1.1"] ; # 
  fhir:name [ fhir:v "SSF1leukemiaCS"] ; # 
  fhir:title [ fhir:v "SSF1 白血病-白血病染色體檢查的評估代碼系統"] ; # 
  fhir:status [ fhir:v "active"] ; # 
  fhir:experimental [ fhir:v "false"^^xsd:boolean] ; # 
  fhir:date [ fhir:v "2024-08-01T15:33:47+08:00"^^xsd:dateTime] ; # 
  fhir:publisher [ fhir:v "Kuo"] ; # 
  fhir:contact ( [
fhir:name [ fhir:v "Kuo" ] ;
    ( fhir:telecom [
fhir:system [ fhir:v "url" ] ;
fhir:value [ fhir:v "http://example.org/example-publisher" ]     ] )
  ] ) ; # 
  fhir:description [ fhir:v "Assessment of chromosome study in leukemia Code System"] ; # 
  fhir:caseSensitive [ fhir:v "true"^^xsd:boolean] ; # 
  fhir:content [ fhir:v "complete"] ; # 
  fhir:count [ fhir:v "27"^^xsd:nonNegativeInteger] ; # 
  fhir:concept ( [
fhir:code [ fhir:v "000" ] ;
fhir:display [ fhir:v "正常" ]
  ] [
fhir:code [ fhir:v "001" ] ;
fhir:display [ fhir:v "AML with t(8;21)(q22;q22.1" ]
  ] [
fhir:code [ fhir:v "002" ] ;
fhir:display [ fhir:v "AML with inv(16)(p13.1q22) or t(16;16)(p13.1;q22)" ]
  ] [
fhir:code [ fhir:v "003" ] ;
fhir:display [ fhir:v "Acute promyelocytic leukemia with t(15;17)" ]
  ] [
fhir:code [ fhir:v "004" ] ;
fhir:display [ fhir:v "AML with t(9;11)(p21.3;q23.3)" ]
  ] [
fhir:code [ fhir:v "005" ] ;
fhir:display [ fhir:v "AML with t(6;9)(p23;q34.1)" ]
  ] [
fhir:code [ fhir:v "006" ] ;
fhir:display [ fhir:v "AML with inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2)" ]
  ] [
fhir:code [ fhir:v "007" ] ;
fhir:display [ fhir:v "AML (megakaryoblastic) with t(1;22)(p13.3;q13.1)" ]
  ] [
fhir:code [ fhir:v "013" ] ;
fhir:display [ fhir:v "AML with t(9;22)(q34;q11)" ]
  ] [
fhir:code [ fhir:v "021" ] ;
fhir:display [ fhir:v "B lymphoblastic leukemia / lymphoma with t(9;22)(q34.1;q11.2)" ]
  ] [
fhir:code [ fhir:v "022" ] ;
fhir:display [ fhir:v "B lymphoblastic leukemia / lymphoma with t(v;11q23.3)" ]
  ] [
fhir:code [ fhir:v "023" ] ;
fhir:display [ fhir:v "B lymphoblastic leukemia / lymphoma with t(12;21)(p13.2;q22.1)" ]
  ] [
fhir:code [ fhir:v "024" ] ;
fhir:display [ fhir:v "B lymphoblastic leukemia / lymphoma with hyperdiploidy" ]
  ] [
fhir:code [ fhir:v "025" ] ;
fhir:display [ fhir:v "B lymphoblastic leukemia / lymphoma with hypodiploidy (hypodiploid ALL)" ]
  ] [
fhir:code [ fhir:v "026" ] ;
fhir:display [ fhir:v "B lymphoblastic leukemia / lymphoma with t(5;14)(q31.1;q32.1)" ]
  ] [
fhir:code [ fhir:v "027" ] ;
fhir:display [ fhir:v "B lymphoblastic leukemia / lymphoma with t(1;19)(q23;p13.3)" ]
  ] [
fhir:code [ fhir:v "041" ] ;
fhir:display [ fhir:v "Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)" ]
  ] [
fhir:code [ fhir:v "042" ] ;
fhir:display [ fhir:v "Mixed phenotype acute leukemia with t(v;11q23.3)" ]
  ] [
fhir:code [ fhir:v "051" ] ;
fhir:display [ fhir:v "Chronic myelogenous leukemia，t(9;22)" ]
  ] [
fhir:code [ fhir:v "061" ] ;
fhir:display [ fhir:v "Myelodysplastic syndrome associated with isolated del(5q-)" ]
  ] [
fhir:code [ fhir:v "090" ] ;
fhir:display [ fhir:v "(1) 一種異常，其他上述未列之染色體異常 (2) 二種異常，其中一種非上述之染色體異常 (3) 二種異常，二種皆非上述之染色體異常" ]
  ] [
fhir:code [ fhir:v "091" ] ;
fhir:display [ fhir:v "同時有兩種上述之染色體異常" ]
  ] [
fhir:code [ fhir:v "092" ] ;
fhir:display [ fhir:v "複雜之染色體異常，指三項(含)以上的染色體變化者" ]
  ] [
fhir:code [ fhir:v "8XX" ] ;
fhir:display [ fhir:v "Chromosome study after chemotherapy or immunotherapy or target therapy" ]
  ] [
fhir:code [ fhir:v "988" ] ;
fhir:display [ fhir:v "不適用。(1) ICD-O-3 M-9811-9837 (EXCEPT C42.0, 42.1, 42.4)" ]
  ] [
fhir:code [ fhir:v "998" ] ;
fhir:display [ fhir:v "有執行染色體檢查，但結果無法判斷" ]
  ] [
fhir:code [ fhir:v "999" ] ;
fhir:display [ fhir:v "病歷未記載或不詳或未執行染色體檢查" ]
  ] ) . #