Weaver Syndrome (WVS)

Alias:
Weaver-Williams Syndrome
Weaver-Smith Syndrome
Wss
Camptodactyly-Overgrowth-Unusual Facies Syndrome
Weaver-Like Syndrome
Wvs
Camptodactyly-Overgrowth-Unusual Facies
Camptodactyly Overgrowth Unusual Facies
Weaver Syndrome, Type 2
Weaver Syndrome 1
Weaver Syndrome 2
Wvs1
Wvs2
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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
韦弗综合症,也被称为韦弗-威廉姆斯综合症,与过度生长综合症和索托斯综合症有关,症状包括肌肉痉挛。韦弗综合症的一个重要基因是EZH2(增强子Zeste 2复合物2亚基),与其相关的途径/超级途径包括基因表达(转录)和RNA聚合酶I启动子开放。附属组织包括骨和皮肤,相关表型包括小头畸形和腭裂。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
常显
胎儿期
<1/1000000
43
343
81

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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