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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
Farber Lipogranulomatosis (FRBRL)
Alias:
Farber Disease
Acid Ceramidase Deficiency
Ceramidase Deficiency
N-Laurylsphingosine Deacylase Deficiency
Farber's Disease
Ac Deficiency
Frbrl
Acylsphingosine Deacylase Deficiency
Farber's Lipogranulomatosis
Farber-Uzman Syndrome
Acy
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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
法布雷病,又称法布雷病,与脂肪肉芽肿和联合溶酶体蛋白缺乏症有关,症状包括疼痛性肿胀关节。法布雷病相关的重要基因是ASAH1(N-酰基鞘氨醇酰胺水解酶1),其相关通路/超通路包括代谢和鞘脂代谢。附属组织包括皮肤和眼睛,相关表型为关节炎和屈曲挛缩。
Related ID:
MALACARDS:FRB001
OMIM:228000
MESH:D055577
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
胎儿期
<1/1000000
16
117
23
FRB001
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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