Van Den Ende-Gupta Syndrome (VDEGS)

Alias:
Vdegs
Marden-Walker-Like Syndrome
Blepharophimosis, Arachnodactyly, and Congenital Contractures
Marden-Walker-Like Syndrome Without Psychomotor Retardation
Marden Walker Like Syndrome
Blepharophimosis Arachnodactyly and Congenital Contractures
Marden-Walker-Like Syndrome Without Psychmotor Retardation
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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
范登恩-古普塔综合症,也称为vdegs,与先天性心脏病和骨骼畸形综合症以及22q11.2染色体缺失综合症有关,末端,并且有症状包括喘息。与范登恩-古普塔综合症有关的重要基因是SCARF2(Scavenger Receptor Class F Member 2),其相关通路/超级通路包括22q11.2拷贝数变异综合症。附属组织包括骨和肺,相关表型为硬角膜和翻转下唇胭脂红。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
16
97
13

Medical Symptom

#
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
Phase
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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