Home Page |
References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 18-10-2022 |
Symbol | CMD1LL |
Location | 22q11.21 |
Name | cardiomyopathy, dilated, 1LL |
Corresponding gene | TXNRD2 |
Main clinical features | nonsyndromic dilated cardiomyopathy |
Genetic determination | not applicable |
Function/system disorder | cardiovascular |
Type | disease |
Remark(s) |