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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
罕见病
Combined Cellular and Humoral Immune Defects with Granulomas (CCHIDG)
Alias:
Combined Immunodeficiency Due to Rag 1/2 Deficiency
Combined Immunodeficiency with Skin Granulomas
Combined Immunodeficiency with Granulomatosis
Cid Due to Rag 1/2 Deficiency
Cchidg
Immune Defects, Combined Cellular and Humoral with Granulomas
Chidg
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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
联合细胞和体液免疫缺陷伴肉芽肿,也称为Rag1/2缺陷引起的严重联合免疫缺陷,与严重联合免疫缺陷、常染色体隐性、T细胞阴性、B细胞阳性、NK细胞阴性和对电离辐射敏感有关。联合细胞和体液免疫缺陷伴肉芽肿相关的重要基因是RAG2(重组激活2),其相关通路/超级通路包括白细胞介素-7信号通路。相关组织包括皮肤和T细胞,相关表型包括反复呼吸道感染和循环IgG水平降低。
Related ID:
MALACARDS:CMB022
OMIM:233650
MESH:C567115
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
--
10
110
111
CMB022
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
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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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