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
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b (LGMD3)
Alias:
Limb-Girdle Muscular Dystrophy Due to Dysferlin Deficiency
Lgmd2b
Dysferlin-Related Limb-Girdle Muscular Dystrophy R2
Limb-Girdle Muscular Dystrophy Type 2b
Lgmd Due to Dysferlin Deficiency
Dysferlin-Related Lgmd R2
Lgmd Type 2b
Muscular Dystrophy, Limb-Girdle, Type 2b
Limb-Girdle Muscular Dystrophy Type 3
Lgmd3
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
常染色体隐性肢带型肌肉萎缩症2b,也称为由于肌钙蛋白缺乏引起的肢带型肌肉萎缩症,与肌肉萎缩症、肢带型、常染色体显性3和肌炎有关。与常染色体隐性肢带型肌肉萎缩症2b有关的重要基因是DYSF(肌钙蛋白),其相关通路/超通路包括心传导和DREAM抑制和杜氏表达。在该疾病的背景下,已经提到了Deflazacort和免疫抑制剂。附属组织包括骨骼肌和单核细胞,相关表型为循环肌酸激酶浓度升高和下肢近端肌肉无力。
Related ID:
MALACARDS:ATS298
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
未知
1-9/1000000
28
272
89
ATS298
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