Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 (ARVD3)

Alias:
Arrhythmogenic Right Ventricular Dysplasia 3
Arrhythmogenic Right Ventricular Cardiomyopathy 3
Arvd3
Arvc3
Familial Arrhythmogenic Right Ventricular Dysplasia 3
Arrhythmogenic Right Ventricular Dysplasia-3
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Arrhythmogenic Right Ventricular Dysplasia, Familial, 3, also known as arrhythmogenic right ventricular dysplasia 3, is related to arrhythmogenic right ventricular cardiomyopathy and meier-gorlin syndrome 1. An important gene associated with Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 is ARVD3 (Arrhythmogenic Right Ventricular Dysplasia 3), and among its related pathways/superpathways is Epithelial to mesenchymal transition in colorectal cancer. Affiliated tissues include heart, and related phenotypes are ventricular arrhythmia and right ventricular cardiomyopathy

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
--
5
36
1

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