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
非罕见病
Schuurs-Hoeijmakers Syndrome (SHMS)
Alias:
Mrd17
Shms
Intellectual Developmental Disorder, Autosomal Dominant 17
Mental Retardation, Autosomal Dominant 17
Autosomal Dominant Mental Retardation 17
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
舒尔-霍伊梅克尔综合症,也被称为mrd17,与内眦赘皮和宽眼距有关,症状包括便秘和癫痫发作。与舒尔-霍伊梅克尔综合症有关的重要基因是PACS1(磷脂酸酸性簇分拣蛋白1),其相关通路/超级通路包括神经科学和L1和Ankyrins之间的相互作用。附属组织包括大脑和B细胞,相关表型为心脏隔膜形态异常和小脑发育不良。
Related ID:
MALACARDS:SCH074
OMIM:615009
MESH:D008607
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
新生儿
--
15
114
10
SCH074
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