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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
Legius Syndrome (LGSS)
Alias:
Neurofibromatosis Type 1-Like Syndrome
Neurofibromatosis 1-Like Syndrome
Nf1-Like Syndrome
Lgss
Nfls
Neurofibromatosis, Type 1-Like Syndrome
Nonmosaic Legius Syndrome
Nonmosaic Lgss
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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
Legius 综合症,也被称为神经纤维瘤病1型类似综合症,与 Noonan 综合症1和 Noonan 综合症伴有多个色素沉着斑有关。Legius 综合症相关的重要基因是SPRED1(Sprouty 相关EVIH1域包含1),其相关通路/超级通路包括EPO诱导的Jak-STAT通路和MAP激酶信号通路。相关组织包括皮肤和肺,相关表型包括多个咖啡斑和特定学习障碍。
Related ID:
MALACARDS:LGS001
OMIM:611431
MESH:C548032
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
新生儿
1-9/100000
4
41
44
LGS001
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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