Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 (ARVD11)

Alias:

Arrhythmogenic Right Ventricular Dysplasia 11

Arrhythmogenic Right Ventricular Dysplasia 11 with Mild Palmoplantar Keratoderma and Woolly Hair

Arrhythmogenic Right Ventricular Cardiomyopathy 11

Arvd11

Arvc11

Arrhythmogenic Right Ventricular Dysplasia, Familial, 11, with Mild Palmoplantar Keratoderma and Woolly Hair

Arrhythmogenic Right Ventricular Dysplasia 11, Familial, and Mild Palmoplantar Keratoderma and Woolly Hair

Arvd and Mild Palmoplantar Keratoderma with or Without Woolly Hair

Familial Arrhythmogenic Right Ventricular Dysplasia 11

Dysplasia, Ventricular, Right, Arrhythmogenic, Type 11

Arvd11pk

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Arrhythmogenic Right Ventricular Dysplasia, Familial, 11, also known as arrhythmogenic right ventricular dysplasia 11, is related to acantholytic acanthoma and lung clear cell carcinoma, and has symptoms including dyspnea and syncope. An important gene associated with Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 is DSC2 (Desmocollin 2), and among its related pathways/superpathways are Nervous system development and DREAM Repression and Dynorphin Expression. Affiliated tissues include heart and heart-ventricle, and related phenotypes are sudden cardiac death and palpitations

Related ID：

MALACARDS：ARR027

OMIM：610476

MESH：D007645