Arthrogryposis Multiplex Congenita 1, Neurogenic, with Myelin Defect (AMC1)

Alias:
Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect
Amcnmy
Amc1
Favorite
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:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
--
1
8
1

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!
微信
信息比对
科研助手
使用教程
回到顶部