Spinocerebellar Ataxia 4 (SCA4)

Alias:
Spinocerebellar Ataxia Type 4
Sca4
Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy
Spinocerebellar Ataxia-4
Spinocerebellar Ataxias
Favorite
基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
脊髓小脑性共济失调4型,又称脊髓小脑性共济失调4型,与脊髓小脑性共济失调4型、常染色体隐性4型和脊髓小脑性共济失调13型有关。与脊髓小脑性共济失调4型有关的重要基因是PLEKHG4(Pleckstrin Homology And RhoGEF Domain Containing G4)。在该疾病的背景下,TA 0910和Nootropic Agents药物已被提及。附属组织包括小脑和皮质,相关表型为振动感觉障碍和本体感觉障碍。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
成年期
--
6
35
3

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!
微信
信息比对
科研助手
使用教程
回到顶部