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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
Robinow Syndrome, Autosomal Dominant 2 (DRS2)
Alias:
Autosomal Dominant Robinow Syndrome 2
Drs2
Robinow, Autosomal Dominant Syndrome, Type 2
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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
罗宾伍综合征,常染色体显性2型,也称为常染色体显性罗宾伍综合征2型,与畸形2型和畸形1型有关。罗宾伍综合征,常染色体显性2型的一个重要基因是DVL1(Dishevelled段极性蛋白1),其相关通路/超级通路包括CTNNB1 S33突变体未被磷酸化和乳腺癌通路。相关组织包括骨和心脏,相关表型包括脐疝和感觉神经性听力障碍。
Related ID:
MALACARDS:RBN017
OMIM:616331
MESH:D004392
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
未知
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13
73
7
RBN017
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Gene & Mutation
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