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
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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:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
未知
1-9/1000000
25
265
52

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!
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