4A01.1Y
其他特指的联合免疫缺陷
Other specified combined immunodeficiencies
- 上级条目
- 4A01.1 联合免疫缺陷
- 层级
- 5 级
索引词 可用于检索该条目的同义词与别名
- 其他特指的联合免疫缺陷
- ORAI1缺乏引起的联合免疫缺陷
- STIM1缺乏引起的联合免疫缺陷
- 部分RAG1缺陷引起的联合免疫缺陷T+B+
- 嘌呤核苷磷酸化酶缺陷引起的免疫缺陷
- NP[核苷磷酸化酶]缺乏症
- PNP[嘌呤核苷磷酸化酶]缺乏症
- 肌苷磷酸化酶缺乏症
- 嘌呤核苷磷酸化酶缺乏症
- 核苷磷酸化酶缺乏症
- 严重联合免疫缺陷-小头畸形-生长迟缓-对电离辐射敏感
- NHEJ1[非同源末端连接因子]综合征
- Cernunnos蛋白缺陷引起的联合免疫缺陷
- DNA连接酶IV缺陷
- LIG4缺陷
- 连接酶4综合征
- CRAC通道功能障碍引起的联合免疫缺陷
- 钙内流缺陷性T细胞失活引起的免疫功能障碍
- ZAP70缺陷引起的联合免疫缺陷
- ζ相关性蛋白70缺乏
- 严重T细胞免疫缺陷-先天性秃发-甲营养不良
- 翼状螺旋缺陷引起的SCID[严重联合免疫缺陷]
- CD3 γ缺陷引起的联合免疫缺陷
- 家族性CD8缺陷
- 与CD8 α链突变相关的呼吸道感染易感性
- 原发性免疫缺陷伴皮肤肉芽肿
- 细胞、体液联合免疫缺陷与多发性肉芽肿
- DOCK8缺陷引起的联合免疫缺陷
- DOCK8[胞质分裂贡献者8蛋白]缺陷引起的CID[联合免疫缺陷]
- DOCK8[胞质分裂专一物8蛋白]缺陷引起的CID[联合免疫缺陷]
- IKZF1突变引起的全血细胞减少症
- Ikaros缺陷引起的CID[联合免疫缺陷]
- X连锁免疫缺陷伴镁缺乏、EB病毒感染或肿瘤形成
- MAGT1缺陷引起的CID[联合免疫缺陷]
- MAGT1缺陷引起的联合免疫缺陷
- CD40配体缺陷引起的高IgM综合征
- HIGM1[高IgM综合征1型]
- 高IgM综合征1型
- CD40L缺陷引起的高IgM综合征
- X连锁高IgM综合征
- CD40缺陷引起的高IgM综合征
- HIGM3[高IgM综合征3型]
- 高IgM综合征3型
- 联合免疫缺陷伴面部-眼-骨骼异常
- 胼胝体发育不全-白内障-免疫缺陷
- Dionisi-Vici-Sabetta-Gambarara综合征
- Vici综合征
- 拇指缺如-身材矮小-免疫缺陷
- 高IgM综合征伴易患机会性感染
- 无机会性感染的高IgM综合征
英文词条（49）
- Other specified combined immunodeficiencies
- Combined immunodeficiency due to ORAI1 deficiency
- Combined immunodeficiency due to STIM1 deficiency
- Combined immunodeficiency T+ B+ due to partial RAG1 deficiency
- Immunodeficiency due to purine nucleoside phosphorylase deficiency
- NP - [nucleoside phosphorylase] deficiency
- Nucleoside phosphorylase deficiency
- PNP - [purine nucleoside phosphorylase] deficiency
- deficiency of inosine phosphorylase
- deficiency of purine-nucleoside phosphorylase
- Severe combined immunodeficiency - microcephaly - growth retardation - sensitivity to ionizing radiation
- Combined immunodeficiency due to Cernunnos protein deficiency
- NHEJ1 - [non-homologous end joining factor] syndrome
- DNA-ligase IV deficiency
- LIG4 deficiency
- Ligase 4 syndrome
- Combined immunodeficiency due to CRAC channel dysfunction
- Immune dysfunction due to T-cell inactivation due to calcium entry defect
- Combined immunodeficiency due to ZAP70 deficiency
- Zeta-associated-protein 70 deficiency
- Severe T-cell immunodeficiency - congenital alopecia - nail dystrophy
- SCID - [Severe combined immunodeficiency] due to winged helix deficiency
- Combined immunodeficiency due to CD3 gamma deficiency
- Familial CD8 deficiency
- Susceptibility to respiratory infections associated with CD8 alpha chain mutation
- Primary immunodeficiency with skin granulomas
- Combined cellular and humoral deficiencies and multiple granulomas
- Combined immunodeficiency due to DOCK8 deficiency
- CID - [combined immunodeficiency] due to DOCK8 - [dedicator of cytokinesis 8 protein] deficiency
- Pancytopenia due to IKZF1 mutations
- CID - [combined immunodeficiency] due to Ikaros deficiency
- X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection or neoplasia
- CID - [combined immunodeficiency] due to MAGT1 deficiency
- Combined immunodeficiency due to MAGT1 deficiency
- Hyper-IgM syndrome due to CD40 ligand deficiency
- HIGM1 - [hyper-IgM syndrome type 1]
- Hyper-IgM syndrome due to CD40L deficiency
- Hyper-IgM syndrome type 1
- X-linked hyper-IgM syndrome
- Hyper-IgM syndrome due to CD40 deficiency
- HIGM3 - [hyper-IgM syndrome type 3]
- Hyper-IgM syndrome type 3
- Combined immunodeficiency with facio-oculo-skeletal anomalies
- Corpus callosum agenesis – cataract – immunodeficiency
- Dionisi-Vici-Sabetta-Gambarara syndrome
- Vici syndrome
- Absent thumb - short stature - immune deficiency
- Hyper-IgM syndrome with susceptibility to opportunistic infections
- Hyper-IgM syndrome without susceptibility to opportunistic infections
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。