Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form

Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form(来自ICD-11)

别称:

Familial Isolated Arrhythmogenic Ventricular Cardiomyopathy, Right Dominant Form

Familial Isolated Arrhythmogenic Ventricular Cardiomyopathy, Classic Form

Familial Isolated Arrhythmogenic Ventricular Dysplasia, Classic Form

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form, also known as familial isolated arrhythmogenic ventricular cardiomyopathy, right dominant form, is related to lethal acantholytic erosive disorder and benign chronic pemphigus. An important gene associated with Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form is CDH2 (Cadherin 2), and among its related pathways/superpathways are Sertoli-Sertoli Cell Junction Dynamics and Keratinization. Affiliated tissues include heart, and related phenotypes are muscle and growth/size/body region

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