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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
Amed Syndrome, Digenic (AMEDS)
Alias:
Amed Syndrome
Ameds
Bone Marrow Failure Syndrome 7, Digenic
Bmfs7
Aplastic Anemia-Intellectual Disability-Dwarfism Syndrome
Aldehyde Degradation Deficiency Syndrome
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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
Amed 综合症,二基因,也被称为 Amed 综合症,与酒精依赖和范可尼贫血,补充组 A 有关。与 Amed 综合症,二基因相关的基因是 ADH5(乙醇脱氢酶 5(III 类),Chi 肽),其相关通路/超通路包括代谢途径生物转化阶段 I 和 II 和由细胞色素 P450 进行的氧化。在该疾病的背景下提到了苯佐卡因和单宁酸。附属组织包括骨髓和骨,相关表型为智力障碍和矮小。
Related ID:
MALACARDS:AMD002
OMIM:619151
MESH:D000080983
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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未知
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8
52
15
AMD002
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
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IF
No Data Found!
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