Home Page |
References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 09-08-2010 |
Symbol | GSD15 |
Location | 3q24 |
Name | glycogen storage disease, type XV |
Other name(s) |
|
Corresponding gene | GYG1 |
Main clinical features | depletion of glycogen in skeletal muscle and cardiac arrhythmias, associated with the accumulation of abnormal storage material in the heart (Moslemi 2010) |
Genetic determination | |
Function/system disorder | metabolism/carbohydrates |
Type | disease |
Remark(s) |