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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
Epilepsy, Myoclonic Juvenile (EJM)
Alias:
Juvenile Myoclonic Epilepsy
Janz Syndrome
Myoclonic Epilepsy, Juvenile, Susceptibility to, 1
Jme
Myoclonic Epilepsy, Juvenile
Juvenile Myoclonus Epilepsy
Petit Mal, Impulsive
Ejm
Susceptibility to Juvenile Myoclonic Epilepsy 1
Jme - [juvenile Myoclonic Epilepsy]
Myoclonic Epilepsy, Juvenile 1
Adolescent Myoclonic Epilepsy
Juvenile Myoclonic Epilepsy 1
Epilepsy, Myoclonic, Juvenile
Myoclonic Epilepsy Juvenile
Myoclonic Epilepsy of Janz
Petit Mal Impulsive
Ejm1
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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
癫痫,肌阵挛性少年型,又称为少年肌阵挛性癫痫,与肌阵挛性癫痫、少年4型癫痫和特发性全面性癫痫有关,症状包括肌阵挛和失神发作。与癫痫,肌阵挛性少年型相关的基因是EFHC1(EF-Hand Domain Containing 1),其相关通路/超级通路包括化学突触间的传递和GABA B受体激活。相关组织包括脑和眼,相关表型为全面性发作和EEG伴有多棘波复合体。
Related ID:
MALACARDS:EPL198
OMIM:254770
MESH:D020190
ICD11:1014397110
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
常显
青少年
--
90
820
20
EPL198
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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