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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 2 (MCAHS2)
Alias:
Glycosylphosphatidylinositol Biosynthesis Defect 4
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 2
Developmental and Epileptic Encephalopathy 20
Epileptic Encephalopathy, Early Infantile, 20
Mcahs Type 2
Mcahs2
Eiee20
Gpibd4
Multiple Congenital Anomalies, Hypotonia, Seizures Syndrome, Type 2
Early Infantile Epileptic Encephalopathy 20
Ferro-Cerebro-Cutaneous Syndrome
Dee20
Fccs
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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2,也称为糖基磷脂酰肌醇合成缺陷4,与低张力和阵发性夜间血红蛋白尿有关,其症状包括肌阵挛性癫痫。与多发性先天性异常-低张力-癫痫综合征2有关的重要基因是PIGA(磷脂酰肌醇糖基化锚定生物合成类A),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脑桥,相关表型为肝大和小头畸形。
Related ID:
MALACARDS:MLT128
OMIM:300868
MESH:D000015
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
X染色体
X显
胎儿期
<1/1000000
13
63
24
MLT128
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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