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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
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome
Alias:
Pign-Cdg
Congenital Disorder of Glycosylation Due to Pign Deficiency
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 1
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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
多发性先天性异常-低张力-癫痫综合征,也称为pig-cdg,与多发性先天性异常-低张力-癫痫综合征4和多发性先天性异常-低张力-癫痫综合征3有关,其症状包括肌肉痉挛、癫痫和震颤。与多发性先天性异常-低张力-癫痫综合征相关的重要基因是PIGN(磷脂酰肌醇糖苷锚定生物合成类N),其相关通路/超级通路包括蛋白质代谢和翻译后修饰:GPI-锚定蛋白的合成。相关组织包括心脏和睾丸,相关表型为癫痫和眼震。
Related ID:
MALACARDS:MLT140
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
12
67
60
MLT140
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!
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