罕见病知识库 RareSeen

急性髓性白血病

Acute myeloid leukemia

ORPHA:519疾病组

定义 英文原文(暂无中文)

A group of neoplasms arising from precursor cells committed to the myeloid cell-line differentiation. All of them are characterized by clonal expansion of myeloid blasts. They manifest by fever, pallor, anemia, hemorrhages and recurrent infections.

别名

急性髓性白血病

基本事实

发病年龄
各年龄段
患病率
1-9 / 100 000

相关基因 12来自下位疾病

Orphanet 未在本条目上直接标注致病基因。下表由本组所属的下位疾病汇总而来,「来源条目」列给出基因实际标注在哪一个 ORPHA 条目上。

基因名称来源条目
ASXL1ASXL transcriptional regulator 1ORPHA:86845
CEBPACCAAT enhancer binding protein alphaORPHA:319465
DNMT3ADNA methyltransferase 3 alphaORPHA:86845
ERCC6L2ERCC excision repair 6 like 2ORPHA:319465
FLT3fms related receptor tyrosine kinase 3ORPHA:98832
GATA1GATA binding protein 1ORPHA:99887
IDH1isocitrate dehydrogenase (NADP(+)) 1ORPHA:86845
IDH2isocitrate dehydrogenase (NADP(+)) 2ORPHA:86845
KITKIT proto-oncogene, receptor tyrosine kinaseORPHA:98834
NPM1nucleophosmin 1ORPHA:402026
TET2tet methylcytosine dioxygenase 2ORPHA:86845
TGM6transglutaminase 6ORPHA:319465

外部标识与链接

发现这一页有错误?告诉我 · 邮件主题会自动带上本页的 ORPHA 编号

本页数据来源

  • 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
  • 中文病名:Orphanet 中文包,冻结于 2020-06-01
  • 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)