Riddle Syndrome (RIDL)

Alias:
Radiosensitivity-Immunodeficiency-Dysmorphic Features-Learning Difficulties Syndrome
Rnf168 Deficiency
Ridl
Radiosensitivity, Immunodeficiency, Dysmorphic Facial Features, and Learning Difficulties
Radiosensitivity, Immunodeficiency, Dysmorphic Features, and Learning Difficulties
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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
谜语综合症,又称辐射敏感性-免疫缺陷-畸形特征-学习困难综合症,与小脑性共济失调和军团病有关,症状包括共济失调和皮肤干燥。与谜语综合症有关的重要基因是RNF168(环指蛋白168),其相关通路/超级通路包括泛素蛋白酶体介导的激活PAK-2p34的调节和传染病。附属组织包括皮肤和眼睛,相关表型为矮小和免疫缺陷。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
婴儿期
<1/1000000
20
79
3

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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