Immunodeficiency 58 (IMD58)

Alias:
Severe Combined Immunodeficiency Due to Carmil2 Deficiency
Imd58
Combined Immunodeficiency Due to Carmil2 Deficiency
Combined Immunodeficiency Due to Rltpr Deficiency
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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58,也称为因carmil2缺乏导致的严重联合免疫缺陷,与联合免疫缺陷和皮肤念珠菌病有关。与免疫缺陷58有关的重要基因是CARMIL2(Capping Protein Regulator And Myosin 1 Linker 2),其相关通路/超级通路包括NF-κB信号通路和甲状腺激素(甲状腺激素)生成。附属组织包括T细胞和平滑肌,相关表型为生长发育不良和复发性皮肤脓肿形成。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
孩童期
<1/1000000
18
187
4

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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