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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
Ablepharon-Macrostomia Syndrome (AMS)
Alias:
Ablepharon Macrostomia Syndrome
Ams
Eye Abnormalities
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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
Ablepharon-Macrostomia Syndrome(无眼睑-大嘴综合症),又名无眼睑大嘴综合症,与外翻和肌肉萎缩有关,症状包括眼部表现和皮肤干燥。与Ablepharon-Macrostomia Syndrome相关的基因是TWIST2(扭曲家族BHLH转录因子2),其相关通路/超级通路包括嗅觉上皮神经发生调节和心脏前体分化。在该疾病的背景下,已提到的药物有氢化钴胺和核黄素。相关组织包括眼睛和皮肤,相关表型包括语言和语言发展延迟和小耳。
Related ID:
MALACARDS:ABL002
OMIM:200110
MESH:C535557
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
胎儿期
<1/1000000
10
150
13
ABL002
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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