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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
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中文
罕见病
Severe Congenital Neutropenia
Alias:
Congenital Neutropenia
Neutropenia, Severe Congenital
Severe Infantile Genetic Neutropenia
Infantile Genetic Agranulocytosis
Congenital Agranulocytosis
Kostmann's Agranulocytosis
Kostmann's Syndrome
Kostmann Disease
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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
重度先天性中性粒细胞减少症,又名先天性中性粒细胞减少症,与重度先天性中性粒细胞减少症4和中性粒细胞减少症,重度先天性,X连锁有关。与重度先天性中性粒细胞减少症有关的重要基因是CSF3R(粒细胞集落刺激因子3受体),其相关通路/超级通路包括免疫系统中的细胞因子信号通路和PAK通路。在该疾病的背景下提到了药物Alemtuzumab和Busulfan。附属组织包括骨和肝,相关表型为内分泌/外分泌腺和免疫系统。
Related ID:
MALACARDS:SVR003
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
X显
常显
常隐
X染色体
孩童期
1-9/1000000
69
754
5
SVR003
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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