Home Page |
References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 19-11-2019 |
Symbol | ARVD12 |
Location | 17q21 |
Name | arrhythmogenic right ventricular dysplasia, familial, 12 |
Corresponding gene | JUP |
Other symbol(s) | ARVC12 |
Main clinical features | arrhythmias and sudden death, heart-muscle disorder characterized by fibrofatty replacement of cardiac myocytes |
Genetic determination | autosomal dominant |
Function/system disorder | cardiovascular |
Type | disease |
Remark(s) |