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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
Epidermolytic Hyperkeratosis (EI)
Alias:
Bullous Congenital Ichthyosiform Erythroderma
Hyperkeratosis, Epidermolytic
Bcie
Ehk
Bullous Congenital Ichthyosiform Erythroderma of Brock
Autosomal Dominant Epidermolytic Ichthyosis
Bullous Ichthyosiform Erythroderma
Ichthyosis Hystrix Brocq Type
Epidermolytic Ichthyosis
Bullous Ichthyosis
Ei
Bullous Erythroderma Ichthyosiformis Congenita of Brocq
Epidermolytic Palmoplantar Hyperkeratosis
Bullous Erythroderma Ichthyosiforme
Bie
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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
表皮松解性角化过度,又称水疱性先天性鱼鳞病性红皮病,与鱼鳞病、环状表皮松解性角化过度1和西门子鱼鳞病有关,症状包括鳞屑皮肤。与表皮松解性角化过度有关的重要基因是KRT10(角蛋白10),其相关通路/超级通路包括神经系统发育和COPI独立的高尔基体至内质网逆行交通。在该疾病的背景下提到了免疫球蛋白和抗体。附属组织包括皮肤和小肠,相关表型为鱼鳞病和角化过度。
Related ID:
MALACARDS:EPD002
MESH:D017488
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
新生儿
1-9/1000000
30
162
11
EPD002
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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