Ventricular Fibrillation, Paroxysmal Familial, 1 (VF1)

Ventricular Fibrillation, Paroxysmal Familial, 1(来自ICD-11)
别称:
Ventricular Fibrillation
Ventricular Fibrillation, Paroxysmal Familial, Type 1
Ventricular Fibrillation, Familial, 1
Vf1
Ivf
Vf
Susceptibility to Ventricular Fibrillation During Myocardial Infarction
Fibrillation, Ventricular, Paroxysmal, Familial, Type 1
Familial Paroxysmal Ventricular Fibrillation 1
Ventricular Fibrillation Adverse Event
加入收藏
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Ventricular Fibrillation, Paroxysmal Familial, 1, also known as ventricular fibrillation, is related to idiopathic ventricular fibrillation, non brugada type and ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy, and has symptoms including chest pain An important gene associated with Ventricular Fibrillation, Paroxysmal Familial, 1 is SCN5A (Sodium Voltage-Gated Channel Alpha Subunit 5), and among its related pathways/superpathways are Cardiac conduction and Dopamine-DARPP32 Feedback onto cAMP Pathway. The drugs Racepinephrine and Grape have been mentioned in the context of this disorder. Affiliated tissues include heart and thyroid, and related phenotypes are syncope and tachycardia
查看原文 参与反馈
相关ID:
MESH:D014693
ICD11:1662472992

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
--
13
157
6

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