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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
Muscular Dystrophy, Congenital, Megaconial Type (MDCMC)
Alias:
Megaconial Type Congenital Muscular Dystrophy
Congenital Muscular Dystrophy Due to Phosphatidylcholine Biosynthesis Defect
Congenital Muscular Dystrophy with Mitochondrial Structural Abnormalities
Megaconial Congenital Muscular Dystrophy
Congenital Megaconial Myopathy
Muscular Dystrophy, Congenital, with Mitochondrial Structural Abnormalities
Mdcmc
Dystrophy, Muscular, Congenital, Megaconial Type
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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
肌营养不良症,先天性,巨细胞型,又称巨细胞型先天性肌营养不良症,与低张力胱氨酸尿症和肌营养不良症,先天性,lmna相关,有关,症状包括肌肉无力、鸭步和面瘫。与肌营养不良症,先天性,巨细胞型有关的重要基因是CHKB(胆碱激酶β),其相关通路/超级通路包括甘油磷脂合成和PC合成。附属组织包括骨骼肌和心脏,相关表型为智力障碍和肌肉无力。
Related ID:
MALACARDS:MSC028
OMIM:602541
MESH:D009136
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
11
81
11
MSC028
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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