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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
Retinitis Pigmentosa (RP)
Alias:
Rod-Cone Dystrophy
Pigmentary Retinopathy
Rp
Pericentral Pigmentary Retinopathy
Non-Syndromic Retinitis Pigmentosa
Tapetoretinal Degeneration
Retinitis Pigmentosa 1
Rcd
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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
视网膜色素变性,又称视杆视锥病变,与视锥视杆病变2和乌舍综合征有关。与视网膜色素变性有关的重要基因是CRX(视锥视杆同源盒),其相关通路/超级通路包括嗅觉信号通路和视觉光转化通路。维生素A和叶黄素已在该疾病的背景下被提及。附属组织包括眼睛和视网膜,相关表型为智力障碍和眼震。
Related ID:
MALACARDS:RTN008
OMIM:268000
MESH:C538365
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
线粒体
常显
X染色体
X显
常隐
X隐
孩童期
1-5/10000
864
8245
536
RTN008
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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