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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-Dystroglycanopathy , Type C, 12 (MDDGC12)
Alias:
Limb-Girdle Muscular Dystrophy Due to Pomk Deficiency
Muscular Dystrophy-Dystroglycanopathy, Limb-Girdle, Pomk-Related
Mddgc12
Muscular Dystrophy-Dystroglycanopathy Type C12
Lgmd Due to Pomk Deficiency
Muscular Dystrophy-Dystroglycanopathy Limb-Girdle C12
Dystrophy, Muscular, Dystroglycanopathy , Type C12
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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-糖基化病,C型12,也称为由于POMK缺乏导致的肢带型肌营养不良,与先天性肌营养不良-糖基化病A10型和Nemaline肌病11型有关。与肌营养不良-糖基化病,C型12相关的基因是POMK(蛋白O-甲基糖激酶),其相关通路/超级通路包括传染性疾病和蛋白质代谢。相关组织包括骨骼肌,相关表型为新生儿低张力和血清肌酸激酶浓度升高。
Related ID:
MALACARDS:MSC118
OMIM:616094
MESH:D049288
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
婴儿期
<1/1000000
19
134
4
MSC118
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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