Ventricular Fibrillation, Paroxysmal Familial, 1 (VF1)

Alias:
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
Favorite
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
Related ID:
MESH:D014693
ICD11:1662472992

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Unknown
--
13
157
6

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!
Wechat
Comparison
Al agent
Tutorials
Back to top