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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
Coffin-Siris Syndrome 6 (CSS6)
Alias:
Css6
Coffin-Siris Syndrome, Type 6
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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
Coffin-Siris Syndrome 6,也被称为css6,与先天性肌病12和房间隔缺损6有关。与Coffin-Siris Syndrome 6有关的重要基因是ARID2(AT-Rich Interaction Domain 2),其相关通路/超级通路包括翻译后修饰:GPI锚定蛋白的合成和Notch信号通路。附属组织包括肺和皮肤,相关表型为全球发育延迟和矮小。
Related ID:
MALACARDS:CFF011
OMIM:617808
MESH:D000015
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
未知
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7
42
4
CFF011
Medical Symptom
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Gene & Mutation
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MGI
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