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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
Autosomal Recessive Congenital Ichthyosis (LI)
Alias:
Lamellar Ichthyosis
Congenital Ichthyosiform Erythroderma
Congenital Nonbullous Ichthyosiform Erythroderma
Li
Non-Bullous Congenital Ichthyosiform Erythroderma
Erythrodermic Ichthyosis
Ichthyosis, Lamellar
Arci
Cie
Non Bullous Congenital Ichthyosiform Erythroderma
Congenital Non-Bullous Ichthyosiform Erythroderma
Nonbullous Congenital Ichthyosiform Erythroderma
Ichthyosiform Erythroderma Nonbullous Congenital
Ichthyosis, Congenital, Autosomal Recessive
Ichthyosiform Erythroderma, Congenital
Non-Bullous Ichthyosiform Erythroderma
Nonbullous Ichthyosiform Erythroderma
Ichthyosiform Erythroderma Congenital
Congenital Lamellar Ichthyosis
Classic Lamellar Ichthyosis
Collodion Baby Syndrome
Ichthyoses, Lamellar
Collodion Fetus
Collodion Baby
Nbcie
Nbie
Ncie
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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
常染色体隐性先天性鱼鳞病,也称为板层鱼鳞病,与先天性鱼鳞病1型和先天性鱼鳞病4a型有关。与常染色体隐性先天性鱼鳞病有关的重要基因是ALOX12B(花生四烯酸12-脂氧合酶,12R型),其相关通路/超级通路包括角质化和前列腺素2的生物合成和代谢FM。在该疾病的背景下提到了乌司奴单抗和贝扎菲布特。附属组织包括皮肤和眼睛,相关表型为鱼鳞病和指甲异常。
Related ID:
MALACARDS:ATS013
MESH:D017490
ICD11:430849255
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
常显
新生儿
1-9/100000
96
515
88
ATS013
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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