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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
Machado-Joseph Disease (MJD)
Alias:
Sca3
Mjd
Spinocerebellar Ataxia Type 3
Azorean Disease
Spinocerebellar Ataxia 3
Spinocerebellar Atrophy
Nigro-Spino-Dentatal Degeneration with Nuclear Ophthalmoplegia
Azorean Disease of the Nervous System
Nigrospinodentatal Degeneration
Azorean Neurologic Disease
Spinopontine Atrophy
Machado Disease
Spinocerebellar Atrophy Type 3
Spinocerebellar Atrophy Iii
Disease, Machado-Joseph
Ataxia, Spinocerebellar
Azorean Ataxia
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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
马尔科夫-约瑟夫病,又称sca3,与脊髓小脑性共济失调2型和脊髓小脑性共济失调1型有关,症状包括肌肉抽搐、肌肉痉挛和肌肉僵硬。与马尔科夫-约瑟夫病有关的重要基因是ATXN3(Ataxin 3),其相关通路/超级通路包括去泛素化和跨膜转运器障碍。在该疾病的背景下,已提到锂碳酸盐和谷氨酸。附属组织包括脊髓和小脑,相关表型为高反射和异常锥体征。
Related ID:
MALACARDS:MCH002
OMIM:109150
MESH:D017827
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
孩童期
1-9/100000
86
787
203
MCH002
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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