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丙种球蛋白缺乏血症

Agammaglobulinemia

ORPHA:183669疾病组

基本事实

患病率
1-9 / 1 000 000(Europe)

相关基因 15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
BLNKB cell linkerORPHA:33110
BTKBruton tyrosine kinaseORPHA:632
CD79ACD79a moleculeORPHA:33110
CD79BCD79b moleculeORPHA:33110
ELF4E74 like ETS transcription factor 4ORPHA:632
IGHMimmunoglobulin heavy constant muORPHA:33110
IGLL1immunoglobulin lambda like polypeptide 1ORPHA:33110
IKZF1IKAROS family zinc finger 1ORPHA:317473
IL21interleukin 21ORPHA:477661
LRBALPS responsive beige-like anchor proteinORPHA:445018
LRRC8Aleucine rich repeat containing 8 VRAC subunit AORPHA:33110
PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit deltaORPHA:33110
PIK3R1phosphoinositide-3-kinase regulatory subunit 1ORPHA:33110
SPI1Spi-1 proto-oncogeneORPHA:33110
TCF3transcription factor 3ORPHA:33110

外部标识与链接

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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)