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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
非罕见病
Immunodeficiency 18 (IMD18)
Alias:
Immunodeficiency 18, Severe Combined Immunodeficiency Variant
Cd3-Epsilon Deficiency
Imd18
Immunodeficiency 18, Scid Variant
Cd3epsilon Deficiency
Immunodeficiency, Type 18
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基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
免疫缺陷18,也称为cd3-epsilon缺陷,与前体T细胞急性淋巴细胞白血病和白血病有关。与免疫缺陷18有关的重要基因是CD3E(T细胞受体复合物CD3 epsilon亚基),其相关通路/超通路包括磷脂酶C通路和ARP-WASP复合物介导的肌动蛋白核化。附属组织包括骨髓和骨,相关表型为缺陷的T细胞增殖和淋巴细胞减少。
Related ID:
MALACARDS:IMM082
OMIM:615615
MESH:D007153
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
--
11
71
6
IMM082
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
#
Gene
Function
Score
Mutations
No data available
Related Drugs
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available
References Literature
Title
PMID
Journal
Year
IF
No Data Found!
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