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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
非罕见病
Arthrogryposis Multiplex Congenita 1, Neurogenic, with Myelin Defect (AMC1)
Alias:
Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect
Amcnmy
Amc1
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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
先天性多关节挛缩症1型,神经源性,伴有髓鞘缺陷,也称为先天性多关节挛缩症,神经源性,伴有髓鞘缺陷,与先天性多关节挛缩症6有关。与先天性多关节挛缩症1型,神经源性,伴有髓鞘缺陷相关的基因是LGI4(富含亮氨酸重复的LGI家族成员4)。相关组织包括肺和呼吸系统-肺,相关表型为上睑下垂和高腭。
Related ID:
MALACARDS:ART164
OMIM:617468
MESH:D001176
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
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1
8
1
ART164
Medical Symptom
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Gene & Mutation
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Gene
Function
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Mutations
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Name
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No data available
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Category
Name
MGI
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