ICD-11 编码查询_国际疾病分类第 11 版中文版_在线疾病编码检索工具
2A60.0

急性髓系白血病伴重现性遗传学异常

Acute myeloid leukaemia with recurrent genetic abnormalities

上级条目
2A60 急性髓系白血病和相关前体细胞肿瘤
层级
4 级

索引词 可用于检索该条目的同义词与别名

  • 急性髓系白血病伴重现性遗传学异常
  • 急性髓系白血病伴t(8;21)(q22;q22),RUNX1-RUNX1T1
  • 急性髓系白血病伴inv(16)(p13.1q22) 或 t(16;16)(p13.1;q22),CBFB-MYH11
  • 急性早幼粒细胞白血病伴 t(15;17)(q24.1;q21.1),PML-RARA
  • APML[急性早幼粒细胞白血病]
  • 急性早幼粒细胞白血病未提及缓解
  • APL[急性早幼粒细胞白血病]
  • 急性早幼粒细胞白血病完全缓解
  • 急性髓系白血病伴t(9;11)(p22;q23);MLLT3-MLL
  • 急性髓系白血病伴11q23异常,未提及缓解
  • 急性髓系白血病伴 11q23异常
  • 急性髓系白血病伴MLL基因变异
  • 急性髓系白血病伴11q23异常,完全缓解
  • 急性髓系白血病伴 t(6;9)(p23;q34);DEK-NUP214
  • 急性髓系白血病伴inv(3)(q21q26.2) 或 t(3;3)(q21;q26.2);RPN1-EVI1
  • 急性髓系白血病(巨核细胞)t(1;22)(p13;q13);RBM15-MKL1
  • 急性髓系白血病伴NPM1基因突变
  • 急性髓系白血病伴CEBPA基因突变
  • 伴有异常骨髓嗜酸性粒细胞inv(16)(p13q22)或t(16;16)(p13;q22)的急性髓系白血病
  • 急性髓性白血病伴t(8;21)(q22;q22)易位
英文词条(20)
  • Acute myeloid leukaemia with recurrent genetic abnormalities
  • Acute myeloid leukaemia with t(8;21)(q22;q22), RUNX1-RUNX1T1
  • Acute myeloid leukaemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22), CBFB-MYH11
  • Acute promyelocytic leukaemia with t(15;17)(q24.1;q21.1), PML-RARA
  • APL - [acute promyelocytic leukaemia]
  • APML - [acute promyelocytic leukaemia]
  • acute promyelocytic leukaemia without mention of remission
  • Acute promyelocytic leukaemia in complete remission
  • Acute myeloid leukaemia with t(9;11)(p22;q23); MLLT3-MLL
  • Acute myeloid leukaemia with 11q23-abnormality
  • Acute myeloid leukaemia with variation of MLL-gene
  • acute myeloid leukaemia with 11q23-abnormality without mention of remission
  • Acute myeloid leukaemia with 11q23-abnormality in complete remission
  • Acute myeloid leukaemia with t(6;9)(p23;q34); DEK- NUP214
  • Acute myeloid leukaemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1
  • Acute myeloid leukaemia (megakaryoblastic) with t(1;22)(p13;q13); RBM15-MKL1
  • Acute myeloid leukaemia with mutated NPM1
  • Acute myeloid leukaemia with mutated CEBPA
  • Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
  • Acute myeloid leukemia with t(8;21)(q22;q22) translocation

后组配轴 Postcoordination

后组配是在主干编码之后追加的可选扩展轴(如侧别、具体解剖部位、严重程度),用于把「部位 + 侧别 + 病程」等细节一次表达完整。只有标注「必填」的轴在组合编码时必须给出,其余可留空。

  • 组织病理histopathology可选
  • 临床表现hasManifestation可选
  • 严重程度hasSeverity可选