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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
Arthrogryposis Multiplex Congenita 2, Neurogenic Type (AMC2)
Alias:
Arthrogryposis Multiplex Congenita, Neurogenic Type
Arthrogryposis Multiplex Congenita Neurogenic Type
Amc2
Amcn
Neurogenic-Type Arthrogryposis Multiplex Congenita-2
Neurogenic Arthrogryposis Multiplex Congenita
Amc, Neurogenic Type
Arthrogryposis Multiplex Congenita, Neurogenic
Amc Neurogenic Type
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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2型,神经源性,也称为先天性多关节挛缩症,神经源性,与先天性多关节挛缩症1型,神经源性,髓鞘缺陷和先天性多关节挛缩症,肾功能不全和胆汁淤积1型有关。与先天性多关节挛缩症2型,神经源性相关的基因是ERGIC1(内质网-高尔基体中间体1)。附属组织包括脊髓和心脏,相关表型为屈曲挛缩和emg:慢性脱髓鞘迹象
Related ID:
MALACARDS:ART163
OMIM:208100
MESH:C536614
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
--
20
92
18
ART163
Medical Symptom
#
Categorization
Description
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Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
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Gene
Function
Score
Mutations
No data available
Related Drugs
Name
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Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
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Publications
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References Literature
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No Data Found!
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