Home Page |
References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 04-03-2019 |
Symbol | CMD1BB |
Location | 18q12.1 |
Name | Cardiomyopathy, dilated, 1BB |
Corresponding gene | DSG2 |
Main clinical features |
|
Genetic determination | autosomal dominant |
Function/system disorder | cardiovascular |
Type | disease |
Remark(s) |