Myasthenic Syndrome, Congenital, 11, Associated with Acetylcholine Receptor Deficiency (CMS11)

Alias:
Congenital Myasthenic Syndrome 11
Cms11
Myasthenic Syndrome, Congenital, Ie
Cms Ie
Cms1e
Myasthenic Syndrome, Congenital, Type 11, Associated with Acetylcholine Receptor Deficiency
Congenital Myasthenic Syndrome 11 Associated with Acetylcholine Receptor Deficiency
Myasthenic Syndrome, Congenital, Ie, Formerly
Congenital Myasthenic Syndrome 1e
Cms Ie, Formerly
Cms1e, Formerly
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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
肌无力症候群,先天性,11型,与乙酰胆碱受体缺乏有关,又称先天性肌无力症候群11型,与肌无力症候群,先天性,4c型,与乙酰胆碱受体缺乏和脊柱和骨盆发育不良,梅格拉班-达格哈-梅尔基型有关。与肌无力症候群,先天性,11型,与乙酰胆碱受体缺乏有关的重要基因是RAPSN(突触相关蛋白),其相关通路/超通路包括过氧化物酶体脂质代谢和线粒体钙离子转运。相关组织包括骨骼肌,相关表型为眼睑下垂和容易疲劳。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
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13
93
51

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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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!
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