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

CodeSystem: SSF1 白血病-白血病染色體檢查的評估代碼系統

Official URL: https://hapi.fhir.tw/fhir/CodeSystem/ssf-1-leukemia-codesystem Version: 0.1.1
Active as of 2024-08-01 Computable Name: SSF1leukemiaCS

Assessment of chromosome study in leukemia Code System

This Code system is referenced in the content logical definition of the following value sets:

Generated Narrative: CodeSystem ssf-1-leukemia-codesystem

This case-sensitive code system https://hapi.fhir.tw/fhir/CodeSystem/ssf-1-leukemia-codesystem defines the following codes:

CodeDisplay
000 正常
001 AML with t(8;21)(q22;q22.1
002 AML with inv(16)(p13.1q22) or t(16;16)(p13.1;q22)
003 Acute promyelocytic leukemia with t(15;17)
004 AML with t(9;11)(p21.3;q23.3)
005 AML with t(6;9)(p23;q34.1)
006 AML with inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2)
007 AML (megakaryoblastic) with t(1;22)(p13.3;q13.1)
013 AML with t(9;22)(q34;q11)
021 B lymphoblastic leukemia / lymphoma with t(9;22)(q34.1;q11.2)
022 B lymphoblastic leukemia / lymphoma with t(v;11q23.3)
023 B lymphoblastic leukemia / lymphoma with t(12;21)(p13.2;q22.1)
024 B lymphoblastic leukemia / lymphoma with hyperdiploidy
025 B lymphoblastic leukemia / lymphoma with hypodiploidy (hypodiploid ALL)
026 B lymphoblastic leukemia / lymphoma with t(5;14)(q31.1;q32.1)
027 B lymphoblastic leukemia / lymphoma with t(1;19)(q23;p13.3)
041 Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)
042 Mixed phenotype acute leukemia with t(v;11q23.3)
051 Chronic myelogenous leukemia，t(9;22)
061 Myelodysplastic syndrome associated with isolated del(5q-)
090 (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
091 同時有兩種上述之染色體異常
092 複雜之染色體異常，指三項(含)以上的染色體變化者
8XX Chromosome study after chemotherapy or immunotherapy or target therapy
988 不適用。(1) ICD-O-3 M-9811-9837 (EXCEPT C42.0, 42.1, 42.4)
998 有執行染色體檢查，但結果無法判斷
999 病歷未記載或不詳或未執行染色體檢查