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
Alport Syndrome
Alias:
Hereditary Nephritis
Alport Hearing Loss-Nephropathy
Alport Deafness-Nephropathy
Hereditary Familial Congenital Hemorrhagic Nephritis
Hematuria-Nephropathy-Deafness Syndrome
Hereditary Interstitial Pyelonephritis
Thin Basement Membrane Nephropathy
Hemorrhagic Hereditary Nephritis
Congenital Hereditary Hematuria
Thin Basement Membrane Disease
Hematuric Hereditary Nephritis
Hemorrhagic Familial Nephritis
Hereditary Hematuria Syndrome
Nephritis, Hereditary
Familial Nephritis
Alports Syndrome
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
Alport 综合症,也被称为遗传性肾炎,与 amme 复合物和 alport 综合症 2,常染色体隐性相关。与 Alport 综合症相关的一个重要基因是 COL4A5(IV 型胶原α5链),其相关通路/超级通路包括 ERK 信号通路和整合素通路。在该疾病的背景下,已提到的药物包括二甲双胍和降糖药。相关组织包括肾脏和眼睛,相关表型包括血尿和薄基底膜。
Related ID:
MALACARDS:ALP004
MESH:D009394
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
X隐
常隐
常显
X染色体
孩童期
1-9/100000
63
605
65
ALP004
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