4A00.2
对特定病原体的遗传学易感性
Genetic susceptibility to particular pathogens
- 层级
- 4 级
跨章引用 同一概念在其他章节另有编码
索引词 可用于检索该条目的同义词与别名
- 对特定病原体的遗传学易感性
- 特发性CD4淋巴细胞减少症
- 白细胞介素1受体相关激酶4缺乏引起的免疫缺陷
- IRAK4[白细胞介素1受体相关激酶4缺乏引起的免疫缺陷]
- 肺纤维化-免疫缺陷-性腺发育异常
- 孟德尔遗传易感分枝杆菌病
- MSMD[孟德尔遗传易感分枝杆菌病 ]
- 卡介苗或非典型分枝杆菌引起的特发性感染
- 呈孟德尔遗传的分枝杆菌病
- 孟德尔易感分枝杆菌疾病
- 常染色体隐性孟德尔遗传易感分枝杆菌病
- AR MSMD[常染色体隐性孟德尔遗传易感分枝杆菌病]
- 完全常染色体隐性遗传干扰素γ受体1缺陷病
- 完全AR IFNGR1[完全常染色体隐性遗传干扰素γ受体1]缺陷病
- 部分常染色体隐性遗传干扰素γ受体1缺陷病
- 部分AR IFNGR1[常染色体隐性遗传干扰素γ受体1]缺陷病
- 完全常染色体隐性遗传干扰素γ受体2缺陷病
- 完全AR IFNGR2[常染色体隐性遗传干扰素γ受体2]缺陷病
- 部分常染色体隐性遗传干扰素γ受体2缺陷病
- 部分AR IFNGR2[常染色体隐性遗传干扰素γ受体2]缺陷病
- 常染色体隐性遗传白介素12受体β1链缺陷病
- AR IL12RB1[常染色体隐性遗传白介素12受体β1链]缺陷病
- 常染色体隐性遗传白细胞介素12p40缺陷病
- AR IL12B[常染色体隐性遗传白细胞介素12p40缺陷病]
- 常染色体隐性遗传络氨酸激酶2缺陷病
- 常染色体隐性遗传高IgE综合征伴非典型分枝杆菌病
- 常染色体显性孟德尔遗传易感分枝杆菌病
- AD MSMD[常染色体显性孟德尔遗传易感分枝杆菌病]
- 常染色体显性遗传干扰素γ受体1缺陷病
- AD IFNGR1[常染色体显性遗传干扰素γ受体1]缺陷病
- 常染色体显性遗传Stat1缺陷病
- AD STAT1[常染色体显性遗传Stat1]缺陷病
- 部分信号转导及转录激活因子1缺陷引起的孟德尔遗传易感分枝杆菌病
- 孟德尔遗传易感分枝杆菌病
- X连锁隐性孟德尔遗传易感分枝杆菌病
- XR MSMD[X连锁隐性孟德尔遗传易感分枝杆菌病]
- 单核细胞减少伴感染易感性
- MonoMAC综合征
- MyD88缺陷引起的化脓性细菌感染
英文词条（36）
- Genetic susceptibility to particular pathogens
- Idiopathic CD4 lymphocytopenia
- Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency
- IRAK4 - [interleukin-1 receptor-associated kinase-4 deficiency]
- Lung fibrosis - immunodeficiency - gonadal dysgenesis
- Mendelian susceptibility to mycobacterial diseases
- Idiopathic infection caused by BCG or atypical mycobacteria
- MSMD - [Mendelian susceptibility to mycobacterial diseases]
- Autosomal recessive mendelian susceptibility to mycobacterial diseases
- AR MSMD - [autosomal recessive mendelian susceptibility to mycobacterial diseases]
- Complete autosomal recessive interferon-gamma receptor 1 deficiency
- Complete AR IFNGR1 - [autosomal recessive interferon-gamma receptor 1] deficiency
- Partial autosomal recessive interferon-gamma receptor 1 deficiency
- Partial AR IFNGR1- [autosomal recessive interferon-gamma receptor 1] deficiency
- Complete autosomal recessive interferon-gamma receptor 2 deficiency
- Complete AR IFNGR2 - [autosomal recessive interferon-gamma receptor 2] deficiency
- Partial autosomal recessive interferon-gamma receptor 2 deficiency
- Partial AR IFNGR2 - [autosomal recessive interferon-gamma receptor 2] deficiency
- Autosomal recessive interleukin 12 receptor beta-1 chain deficiency
- AR IL12RB1 - [Autosomal recessive interleukin 12 receptor beta-1 chain] deficiency
- Autosomal recessive interleukin 12p40 deficiency
- AR IL12B - [Autosomal recessive interleukin 12p40] deficiency
- Autosomal recessive tyrosine kinase 2 deficiency
- Autosomal recessive hyper-IgE syndrome with atypical mycobacteriosis
- Autosomal dominant mendelian susceptibility to mycobacterial diseases
- AD MSMD - [Autosomal dominant mendelian susceptibility to mycobacterial diseases]
- Autosomal dominant interferon-gamma receptor 1 deficiency
- AD IFNGR1 - [Autosomal dominant interferon-gamma receptor 1] deficiency
- Autosomal dominant Stat1 deficiency
- AD STAT1 - [Autosomal dominant Stat1] deficiency
- Mendelian susceptibility to mycobacterial diseases due to partial signal transducer and activator of transcription 1 deficiency
- X-linked recessive mendelian susceptibility to mycobacterial diseases
- XR MSMD - [X-linked recessive mendelian susceptibility to mycobacterial diseases]
- Monocytopenia with susceptibility to infections
- MonoMAC syndrome
- Pyogenic bacterial infections due to MyD88 deficiency
后组配轴 Postcoordination
该条目未定义后组配轴，直接使用上面的编码即可。后组配是在主干编码之后追加侧别、具体解剖部位、严重程度、病因等细节的可选组合方式，不是必填项。