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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
Arts Syndrome (ARTS)
Alias:
Ataxia, Fatal X-Linked, with Deafness and Loss of Vision
Lethal Ataxia with Deafness and Optic Atrophy
Mrxsarts
Mrxs18
Arts
Fatal X-Linked Ataxia with Deafness and Loss of Vision
Lethal Ataxia with Hearing Loss and Optic Atrophy
Mental Retardation, X-Linked, Syndromic, Arts Type
Syndromic X-Linked Mental Retardation Arts Type
Mental Retardation, X-Linked, Syndromic 18
Syndromic X-Linked Mental Retardation 18
Ataxia-Deafness-Optic Atrophy, Lethal
Art
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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
艺术综合症,也被称为进行性共济失调、致命性X连锁、伴有耳聋和视力丧失,与Charcot-Marie-Tooth病型5和尿路结石有关,其症状包括共济失调、癫痫发作和未明确的视力丧失。与艺术综合症有关的重要基因是PRPS1(磷酸核糖焦磷酸合成酶1),其相关通路/超级通路包括代谢和核苷酸代谢。在该疾病的背景下,已提到的药物包括乙醇和芳樟醇。相关组织包括脑和眼,相关表型为肌肉无力和视力障碍。
Related ID:
MALACARDS:ART002
OMIM:301835
MESH:C535388
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
X染色体
X显
新生儿
<1/1000000
16
319
8
ART002
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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