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
Smith-Lemli-Opitz Syndrome (SLOS)
Alias:
Slos
7-Dehydrocholesterol Reductase Deficiency
Rsh Syndrome
Rutledge Lethal Multiple Congenital Anomaly Syndrome
Slo Syndrome
Polydactyly, Sex Reversal, Renal Hypoplasia, and Unilobar Lung
Smith-Lemli-Opitz Syndrome, Type Ii
Lethal Acrodysgenital Syndrome
Smith-Opitz-Inborn 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
史密斯-莱姆利-奥普茨综合症,也被称为slos,与格林伯格发育不良和家族性高胆固醇血症1有关,其症状包括便秘、癫痫发作和呕吐。与史密斯-莱姆利-奥普茨综合症有关的重要基因是DHCR7(7-脱氢胆固醇还原酶),其相关通路/超级通路包括代谢和葡萄糖/能量代谢。在该疾病的背景下提到了辛伐他汀和苯佐卡因。附属组织包括肺和眼,相关表型为智力障碍和肌张力低下。
Related ID:
MALACARDS:SMT004
OMIM:270400
MESH:D019082
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
1-9/100000
37
419
227
SMT004
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