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
Hypophosphatasia (HPP)
Alias:
Phosphoethanolaminuria
Deficiency of Alkaline Phosphatase
Childhood Hypophosphatasia
Rathbun Disease
Hpp
Hypophosphatasia, Childhood
Infantile Hypophosphatasia
Hypophospatasia, Childhood
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
低磷酸酶血症,也称为磷酸乙醇胺尿症,与低磷酸酶血症、婴儿期和儿童期有关,症状包括癫痫发作、鸭步和呼吸暂停。与低磷酸酶血症有关的重要基因是ALPL(碱性磷酸酶,生物矿化相关),其相关通路/超级通路包括磷脂酶C通路和受体酪氨酸激酶信号通路。在该疾病的背景下,已提到的药物包括硼替佐米和利妥昔单抗。附属组织包括骨和肾,相关表型为长骨弯曲和牙齿异常。
Related ID:
MALACARDS:HYP035
MESH:C562440
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
常显
全年龄段
<1/1000000
25
208
114
HYP035
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