Pseudobulbar Palsy

Pseudobulbar Palsy(来自ICD-11)
别称:
Pseudobulbar Paralysis
加入收藏
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Pseudobulbar Palsy, also known as pseudobulbar paralysis, is related to cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 and cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2, and has symptoms including dysarthria, dysphagia and spasticity. An important gene associated with Pseudobulbar Palsy is NOTCH3 (Notch Receptor 3), and among its related pathways/superpathways are Neuroscience and Copper homeostasis. Affiliated tissues include tongue and brain, and related phenotypes are Increased shRNA abundance (Z-score > 2) and homeostasis/metabolism
查看原文 参与反馈
相关ID:
MESH:D020828

基础信息

遗传方式
发病时间
患病率/发病率
相关基因
相关模型
参考文献
MALACARDS
--
Unknown
--
17
252
--

疾病表征

#
分类
表征
HPO概率
Orphanet概率
HPO来源
暂无相关数据

基因 & 突变

#
基因
作用分类
分值
突变数量
暂无相关数据

靶点药物

药物名称
CAS号
研发状态
临床阶段
暂无相关数据

疾病模型

类型
名称
MGI
相关基因
品系来源
文献数量
暂无相关数据

文献报道

标题
PMID
期刊
年代
IF
暂无数据
Wechat
Comparison
Al agent
Tutorials
Back to top