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
Hermansky-Pudlak Syndrome 7 (HPS7)
Alias:
Hps7
Albinism with Hemorrhagic Diathesis and Pigmented Reticuloendothelial Cells
Albinism with Hemorrhagic Diathesis and Pigmented Reticuloendothelial
Hermansky-Pudlak Syndrome, Type 7
Platelet Storage Pool Deficiency
Delta Storage Pool Disease
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
赫曼斯基-普德拉克综合症7,也称为hps7,与孤立的δ储存池疾病和赫曼斯基-普德拉克综合症1有关,症状包括腹痛。与赫曼斯基-普德拉克综合症7有关的重要基因是DTNBP1(肌动蛋白结合蛋白1)。在该疾病的背景下,已提到的药物包括吡非尼酮和普拉伐他汀。附属组织包括皮肤和骨髓,相关表型为眼震和视力减退。
Related ID:
MALACARDS:HRM010
OMIM:614076
MESH:D022861
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
--
10
49
4
HRM010
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