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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
Myosclerosis, Autosomal Recessive (MYOSAR)
Alias:
Myosclerosis
Myosclerosis, Congenital
Congenital Myosclerosis, Lowenthal Type
Myosclerosis, Congenital, of Lowenthal
Congenital Myosclerosis of Lowenthal
Myosclerosis Autosomal Recessive
Myopathy, Myosclerotic
Myosclerotic Myopathy
Myosar
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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,常染色体隐性型,也称为肌营养不良症,与系统性硬皮病和胶原VI相关性肌病有关,症状包括面部偏瘫。肌营养不良症,常染色体隐性型的一个重要相关基因是COL6A2(胶原VIα2链)。相关组织包括骨骼肌和心脏,相关表型为循环肌酸激酶浓度升高和跟腱挛缩。
Related ID:
MALACARDS:MYS016
OMIM:255600
MESH:D003095
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
孩童期
--
1
5
3
MYS016
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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