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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
Williams-Beuren Syndrome (WBS)
Alias:
Williams Syndrome
Deletion 7q11.23
Monosomy 7q11.23
Wbs
Chromosome 7q11.23 Deletion Syndrome, 1.5- to 1.8-Mb
Hypercalcemia-Supravalvar Aortic Stenosis
Elfin Facies with Hypercalcemia
Fanconi Schlesinger Syndrome
Elfin Facies Syndrome
Beuren Syndrome
Wms
Ws
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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
威廉姆斯-贝伦综合症,又称威廉姆斯综合症,与超瓣膜性主动脉狭窄和威廉姆斯-贝伦区域重复综合症有关,症状包括超敏、异常体重增加和慢性便秘。与威廉姆斯-贝伦综合症有关的重要基因是ELN(弹性蛋白),其相关通路/超级通路包括7q11.23复制数变异综合症。在该疾病的背景下提到了Buspirone和Dopamine药物。附属组织包括心脏和骨骼,相关表型为智力障碍和高反射。
Related ID:
MALACARDS:WLL001
OMIM:194050
MESH:D018980
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
胎儿期
1-5/10000
140
1130
148
WLL001
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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