Home
Toolbox
Resource
Workflow
Tutorials
Citations
Downloads
Mutation Al-Predictor Flow
Gene-to-Mutation Flow
News & Insights
Genetic Encyclopedia
Frontiers
Industry Insights
Case Studies
About Us
About the Site
Contact Us
Private Policy
User Agreement
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
Log In
|
Sign Up
中文
罕见病
Developmental and Epileptic Encephalopathy 82 (DEE82)
Alias:
Epileptic Encephalopathy, Early Infantile, 82
Dee82
Developmental and Epileptic Encephalopathy, 82
Got2 Deficiency
Eiee82
Glutamate Oxaloacetate Transaminase, Mitochondrial, Deficiency of
Deficiency of Mitochondrial Glutamate Oxaloacetate Transaminase
Early Infantile Epileptic Encephalopathy 82
Create a favorites folder
Cancel
Confirm
Add To Favorites
Select a favorites
Description
New favorites >>
Cancel
Confirm
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
发育性和癫痫性脑病82,也称为癫痫性脑病,早婴儿期,82,与发育性和癫痫性脑病和高同型半胱氨酸血症有关。与发育性和癫痫性脑病82有关的重要基因是GOT2(谷氨酸-天冬氨酸转氨酶2),其相关通路/超级通路包括糖胺聚糖代谢和糖酵解(BioCyc)。附属组织包括大脑,相关表型为癫痫发作和语言发育延迟。
Related ID:
MALACARDS:DVL105
OMIM:618721
MESH:D013036
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
--
2
16
1
DVL105
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