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
Prolidase Deficiency (PD)
Alias:
Hyperimidodipeptiduria
Imidodipeptidase Deficiency
Peptidase Deficiency
Pd
Proline Dipeptidase Deficiency
Deficiency of Prolidase
Imidodipeptiduria
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
脯氨酰二肽酶缺乏症,又称高咪唑二肽尿症,与阵发性极端疼痛障碍和脾肿大有关,症状包括皮肤紫癜。与脯氨酰二肽酶缺乏症相关的重要基因是PEPD(肽酶D),其相关通路/超级通路包括22q11.2拷贝数变异综合征和L-精氨酸代谢的超级通路。附属组织包括皮肤和脾脏,相关表型包括听力障碍和鼻梁下陷。
Related ID:
MALACARDS:PRL019
OMIM:170100
MESH:D056732
ICD11:1416203271
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
14
44
33
PRL019
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