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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
Glycogen Storage Disease Due to Liver Phosphorylase Kinase Deficiency (XLG)
Alias:
Glycogenosis Due to Liver Phosphorylase Kinase Deficiency
Gsd Due to Liver Phosphorylase Kinase Deficiency
Glycogen Storage Disease Type Ixa
Glycogen Storage Disease Type Ixc
Glycogen Storage Disease Type 9a
Glycogen Storage Disease Type 9c
Glycogenosis Type Ixa
Glycogenosis Type Ixc
Glycogenosis Type 9a
Glycogenosis Type 9c
Gsd Type Ixa
Gsd Type Ixc
Gsd Type 9a
Gsd Type 9c
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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
肝磷酸酶激酶缺乏引起的糖原贮积病,也称为肝磷酸酶激酶缺乏引起的糖原病,与糖原贮积病ixa和糖原贮积病ixc有关。与肝磷酸酶激酶缺乏引起的糖原贮积病相关的基因是PHKA2(磷酸酶激酶调节亚基α2),其相关通路/超级通路包括ADORA2B介导的抗炎细胞因子产生和氨基葡萄糖糖苷酶代谢。相关组织包括肝脏和骨骼肌,相关表型为肝大和血清转氨酶升高。
Related ID:
MALACARDS:GLY065
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
X染色体
X显
孩童期
1-9/100000
2
8
--
GLY065
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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