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
Amegakaryocytic Thrombocytopenia, Congenital, 1 (CAMT1)
Alias:
Congenital Amegakaryocytic Thrombocytopenia
Camt
Thrombocytopenia, Congenital Amegakaryocytic
Thrombocytopenia, Megakaryocytic, Congenital, Type 1
Congenital Amegakaryocytic Thrombocytopenic Purpura
Thrombocytopenia, Amegakaryocytic, Congenital
Amegakaryocytic Thrombocytopenia, Congenital
Camt1
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
先天性巨核细胞减少性血小板减少症1型,也称为先天性巨核细胞减少性血小板减少症,与原发性血小板增多症和全血细胞减少症有关。与先天性巨核细胞减少性血小板减少症1型相关的重要基因是MPL(MPL原癌基因,血小板生成素受体),其相关通路/超级通路包括NF-κB信号通路和胚胎和诱导多能干细胞和特异性标记物。在该疾病的背景下,Mechlorethamine和Melphalan已被提及。附属组织包括骨髓和骨,相关表型为异常血红蛋白和血小板减少症。
Related ID:
MALACARDS:AMG002
OMIM:604498
MESH:C535982
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
未知
1-9/1000000
25
265
52
AMG002
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