國家級人體生物資料庫整合平台共同資料模式實作指引(NBCT Common Data Model IG)
1.1.0 - Release1.1.0
國家級人體生物資料庫整合平台共同資料模式實作指引(NBCT Common Data Model IG)
1.1.0 - Release1.1.0
This page is part of the 國家級人體生物資料庫整合平台共同資料模式實作指引(NBCT Common Data Model IG) (v1.1.0: Release) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions
| Active as of 2024-08-01 |
@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 -------------------------------------------------------------------
<http://hl7.org/fhir/CodeSystem/ssf-1-leukemia-codesystem-cs> a fhir:CodeSystem ;
fhir:nodeRole fhir:treeRoot ;
fhir:Resource.id [ fhir:value "ssf-1-leukemia-codesystem-cs"] ;
fhir:Resource.language [ fhir:value "zh-TW"] ;
fhir:DomainResource.text [
fhir:Narrative.status [ fhir:value "generated" ] ;
fhir:Narrative.div "<div xml:lang=\"zh-TW\" xmlns=\"http://www.w3.org/1999/xhtml\" lang=\"zh-TW\"><p class=\"res-header-id\"><b>Generated Narrative: 代码系统 ssf-1-leukemia-codesystem-cs</b></p><a name=\"ssf-1-leukemia-codesystem-cs\"> </a><a name=\"hcssf-1-leukemia-codesystem-cs\"> </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\">Language: zh-TW</p></div><p>This case-sensitive code system <code>https://www.ghd.tw/cdm-fhir/CodeSystem/ssf-1-leukemia-codesystem-cs</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-cs-000\"> </a></td><td>正常</td></tr><tr><td style=\"white-space:nowrap\">001<a name=\"ssf-1-leukemia-codesystem-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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-cs-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:CodeSystem.url [ fhir:value "https://www.ghd.tw/cdm-fhir/CodeSystem/ssf-1-leukemia-codesystem-cs"] ;
fhir:CodeSystem.version [ fhir:value "1.1.0"] ;
fhir:CodeSystem.name [ fhir:value "SSF1leukemiaCS"] ;
fhir:CodeSystem.title [ fhir:value "SSF1 白血病-白血病染色體檢查的評估代碼系統"] ;
fhir:CodeSystem.status [ fhir:value "active"] ;
fhir:CodeSystem.experimental [ fhir:value "false"^^xsd:boolean] ;
fhir:CodeSystem.date [ fhir:value "2024-08-01T15:33:47+08:00"^^xsd:dateTime] ;
fhir:CodeSystem.publisher [ fhir:value "國家衛生研究院"] ;
fhir:CodeSystem.contact [
fhir:index 0 ;
fhir:ContactDetail.name [ fhir:value "國家衛生研究院" ] ;
fhir:ContactDetail.telecom [
fhir:index 0 ;
fhir:ContactPoint.system [ fhir:value "url" ] ;
fhir:ContactPoint.value [ fhir:value "https://ghd.tw/" ]
]
] ;
fhir:CodeSystem.description [ fhir:value "Assessment of chromosome study in leukemia Code System"] ;
fhir:CodeSystem.jurisdiction [
fhir:index 0 ;
fhir:CodeableConcept.coding [
fhir:index 0 ;
fhir:Coding.system [ fhir:value "urn:iso:std:iso:3166" ] ;
fhir:Coding.code [ fhir:value "TW" ]
]
] ;
fhir:CodeSystem.caseSensitive [ fhir:value "true"^^xsd:boolean] ;
fhir:CodeSystem.content [ fhir:value "complete"] ;
fhir:CodeSystem.count [ fhir:value "27"^^xsd:nonNegativeInteger] ;
fhir:CodeSystem.concept [
fhir:index 0 ;
fhir:CodeSystem.concept.code [ fhir:value "000" ] ;
fhir:CodeSystem.concept.display [ fhir:value "正常" ]
], [
fhir:index 1 ;
fhir:CodeSystem.concept.code [ fhir:value "001" ] ;
fhir:CodeSystem.concept.display [ fhir:value "AML with t(8;21)(q22;q22.1" ]
], [
fhir:index 2 ;
fhir:CodeSystem.concept.code [ fhir:value "002" ] ;
fhir:CodeSystem.concept.display [ fhir:value "AML with inv(16)(p13.1q22) or t(16;16)(p13.1;q22)" ]
], [
fhir:index 3 ;
fhir:CodeSystem.concept.code [ fhir:value "003" ] ;
fhir:CodeSystem.concept.display [ fhir:value "Acute promyelocytic leukemia with t(15;17)" ]
], [
fhir:index 4 ;
fhir:CodeSystem.concept.code [ fhir:value "004" ] ;
fhir:CodeSystem.concept.display [ fhir:value "AML with t(9;11)(p21.3;q23.3)" ]
], [
fhir:index 5 ;
fhir:CodeSystem.concept.code [ fhir:value "005" ] ;
fhir:CodeSystem.concept.display [ fhir:value "AML with t(6;9)(p23;q34.1)" ]
], [
fhir:index 6 ;
fhir:CodeSystem.concept.code [ fhir:value "006" ] ;
fhir:CodeSystem.concept.display [ fhir:value "AML with inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2)" ]
], [
fhir:index 7 ;
fhir:CodeSystem.concept.code [ fhir:value "007" ] ;
fhir:CodeSystem.concept.display [ fhir:value "AML (megakaryoblastic) with t(1;22)(p13.3;q13.1)" ]
], [
fhir:index 8 ;
fhir:CodeSystem.concept.code [ fhir:value "013" ] ;
fhir:CodeSystem.concept.display [ fhir:value "AML with t(9;22)(q34;q11)" ]
], [
fhir:index 9 ;
fhir:CodeSystem.concept.code [ fhir:value "021" ] ;
fhir:CodeSystem.concept.display [ fhir:value "B lymphoblastic leukemia / lymphoma with t(9;22)(q34.1;q11.2)" ]
], [
fhir:index 10 ;
fhir:CodeSystem.concept.code [ fhir:value "022" ] ;
fhir:CodeSystem.concept.display [ fhir:value "B lymphoblastic leukemia / lymphoma with t(v;11q23.3)" ]
], [
fhir:index 11 ;
fhir:CodeSystem.concept.code [ fhir:value "023" ] ;
fhir:CodeSystem.concept.display [ fhir:value "B lymphoblastic leukemia / lymphoma with t(12;21)(p13.2;q22.1)" ]
], [
fhir:index 12 ;
fhir:CodeSystem.concept.code [ fhir:value "024" ] ;
fhir:CodeSystem.concept.display [ fhir:value "B lymphoblastic leukemia / lymphoma with hyperdiploidy" ]
], [
fhir:index 13 ;
fhir:CodeSystem.concept.code [ fhir:value "025" ] ;
fhir:CodeSystem.concept.display [ fhir:value "B lymphoblastic leukemia / lymphoma with hypodiploidy (hypodiploid ALL)" ]
], [
fhir:index 14 ;
fhir:CodeSystem.concept.code [ fhir:value "026" ] ;
fhir:CodeSystem.concept.display [ fhir:value "B lymphoblastic leukemia / lymphoma with t(5;14)(q31.1;q32.1)" ]
], [
fhir:index 15 ;
fhir:CodeSystem.concept.code [ fhir:value "027" ] ;
fhir:CodeSystem.concept.display [ fhir:value "B lymphoblastic leukemia / lymphoma with t(1;19)(q23;p13.3)" ]
], [
fhir:index 16 ;
fhir:CodeSystem.concept.code [ fhir:value "041" ] ;
fhir:CodeSystem.concept.display [ fhir:value "Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)" ]
], [
fhir:index 17 ;
fhir:CodeSystem.concept.code [ fhir:value "042" ] ;
fhir:CodeSystem.concept.display [ fhir:value "Mixed phenotype acute leukemia with t(v;11q23.3)" ]
], [
fhir:index 18 ;
fhir:CodeSystem.concept.code [ fhir:value "051" ] ;
fhir:CodeSystem.concept.display [ fhir:value "Chronic myelogenous leukemia，t(9;22)" ]
], [
fhir:index 19 ;
fhir:CodeSystem.concept.code [ fhir:value "061" ] ;
fhir:CodeSystem.concept.display [ fhir:value "Myelodysplastic syndrome associated with isolated del(5q-)" ]
], [
fhir:index 20 ;
fhir:CodeSystem.concept.code [ fhir:value "090" ] ;
fhir:CodeSystem.concept.display [ fhir:value "(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:index 21 ;
fhir:CodeSystem.concept.code [ fhir:value "091" ] ;
fhir:CodeSystem.concept.display [ fhir:value "同時有兩種上述之染色體異常" ]
], [
fhir:index 22 ;
fhir:CodeSystem.concept.code [ fhir:value "092" ] ;
fhir:CodeSystem.concept.display [ fhir:value "複雜之染色體異常，指三項(含)以上的染色體變化者" ]
], [
fhir:index 23 ;
fhir:CodeSystem.concept.code [ fhir:value "8XX" ] ;
fhir:CodeSystem.concept.display [ fhir:value "Chromosome study after chemotherapy or immunotherapy or target therapy" ]
], [
fhir:index 24 ;
fhir:CodeSystem.concept.code [ fhir:value "988" ] ;
fhir:CodeSystem.concept.display [ fhir:value "不適用。(1) ICD-O-3 M-9811-9837 (EXCEPT C42.0, 42.1, 42.4)" ]
], [
fhir:index 25 ;
fhir:CodeSystem.concept.code [ fhir:value "998" ] ;
fhir:CodeSystem.concept.display [ fhir:value "有執行染色體檢查，但結果無法判斷" ]
], [
fhir:index 26 ;
fhir:CodeSystem.concept.code [ fhir:value "999" ] ;
fhir:CodeSystem.concept.display [ fhir:value "病歷未記載或不詳或未執行染色體檢查" ]
] .
# - ontology header ------------------------------------------------------------
<http://hl7.org/fhir/CodeSystem/ssf-1-leukemia-codesystem-cs.ttl> a owl:Ontology ;
owl:imports fhir:fhir.ttl ;
owl:versionIRI <http://build.fhir.org/CodeSystem/ssf-1-leukemia-codesystem-cs.ttl> .
IG © 2026+ 國家衛生研究院. Package tw.nhri.nbct.cdm#1.1.0 based on FHIR 4.0.1. Generated 2026-10-15
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