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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
Myopathy, Centronuclear, 1 (CNM1)
Alias:
Autosomal Dominant Centronuclear Myopathy
Centronuclear Myopathy 1
Ad-Cnm
Cnm1
Centronuclear Myopathy, Autosomal, Modifier of
Myopathy, Centronuclear, Autosomal Dominant
Autosomal Dominant Myotubular Myopathy
Centronuclear Myopathy Autosomal Dominant
Myotubular Myopathy, Autosomal Dominant
Myopathies, Structural, Congenital
Myopathy, Centronuclear, Type 1
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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
肌病,中心核型,1型,也被称为常染色体显性中心核型肌病,与肌病,中心核型,4型和中心核型肌病有关,症状包括面部麻痹和眼肌麻痹。与肌病,中心核型,1型相关的基因是DNM2(Dynamin 2),其相关通路/超级通路包括肌纤维收缩通路和肌细胞生成通路。在该疾病的背景下提到了他莫昔芬和柠檬酸钠。相关组织包括骨骼肌和眼睛,相关表型为中心核型骨骼肌纤维和上睑下垂。
Related ID:
MALACARDS:MYP123
OMIM:160150
MESH:D020914
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
新生儿
--
49
346
22
MYP123
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
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Year
IF
No Data Found!
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