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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
Gaucher Disease, Type I (GD1)
Alias:
Acid Beta-Glucosidase Deficiency
Glucocerebrosidase Deficiency
Gaucher Disease Type 1
Gaucher Disease Type I
Gba Deficiency
Gd I
Gd1
Gaucher Disease, Noncerebral Juvenile
Non-Cerebral Juvenile Gaucher Disease
Gaucher's Disease Type I
Gaucher Disease
Adult Non-Neuronopathic Gaucher Disease
Noncerebral Juvenile Gaucher Disease
Gaucher Disease, Type 1
Type 1 Gaucher Disease
Gaucher Disease 1
Gd
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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
I型戈谢病,又称酸β-葡萄糖苷酶缺乏症,与戈谢病、围产期致死性和遗传性晚期帕金森病有关,症状包括呼吸困难和骨痛。与I型戈谢病有关的重要基因是GBA1(β-葡萄糖苷酶β1),其相关通路/超级通路包括神经科学和鞘脂代谢。在该疾病的背景下提到了利迪帕韦和索非布韦。附属组织包括骨和骨髓,相关表型为骨质疏松和脾肿大
Related ID:
MALACARDS:GCH015
OMIM:230800
MESH:D005776
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
全年龄段
1-9/100000
27
289
234
GCH015
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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