Muscular Dystrophy-Dystroglycanopathy , Type a, 3 (MDDGA3)

Alias:
Muscular Dystrophy-Dystroglycanopathy , Type A3
Mddga3
Muscular Dystrophy-Dystroglycanopathy Congenital with Brain and Eye Anomalies A3
Walker-Warburg Syndrome or Muscle-Eye-Brain Disease, Pomgnt1-Related
Dystrophy, Muscular, Dystroglycanopathy , Type A3
Muscle-Eye-Brain Disease Pomgnt1-Related
Walker-Warburg Syndrome Pomgnt1-Related
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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,类型a,3,也称为肌营养不良-糖基化病,类型a3,与先天性肌营养不良-糖基化病,类型a3和眼脑肌病有关,症状包括癫痫发作。与肌营养不良-糖基化病,类型a,3有关的重要基因是POMGNT1(β1,2-蛋白O-连接的甘露糖N-乙酰葡萄糖苷转移酶1)。附属组织包括眼睛和大脑,相关表型包括脑积水和全球发育延迟。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
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2
11
25

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
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No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
No Data Found!
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