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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
Mandibulofacial Dysostosis with Alopecia (MFDA)
Alias:
Mfda
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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
下颌面发育不全伴脱发,也称为mfda,与特雷彻·柯林斯综合症1和发育不全有关。与下颌面发育不全伴脱发有关的重要基因是EDNRA(内皮素受体类型A),其相关通路/超级通路包括信号转导和GPCR下游信号转导。附属组织包括骨和皮肤,相关表型为脱发和传导性听力障碍。
Related ID:
MALACARDS:MND025
OMIM:616367
MESH:D008342
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
新生儿
<1/1000000
10
67
3
MND025
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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