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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
Witteveen-Kolk Syndrome (WITKOS)
Alias:
Sin3a-Related Intellectual Disability Syndrome Due to a Point Mutation
Witkos
Sin3a-Related Intellectual Disability Syndrome
Witteveen-Kolk Syndrome , 15q24 Del/dup Syndrome
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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
维特文-科尔克综合症,也被称为点突变导致的sin3a相关智力障碍综合症,与15q24染色体缺失综合症和小头畸形有关。与维特文-科尔克综合症相关的重要基因是SIN3A(SIN3转录调节家族成员A),其相关通路/超级通路包括复制前复合物的组装和RNA聚合酶II转录启动和启动子清除。相关组织包括大脑和眼睛,相关表型包括异常面部形状和智力障碍,轻度
Related ID:
MALACARDS:WTT002
OMIM:613406
MESH:D000015
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
胎儿期
<1/1000000
2
10
11
WTT002
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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