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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 30/03/2006 |
Symbol | CMD1G |
Location | 2q24.3-q31 |
Name | cardiomyopathy, dilated 1G |
Corresponding gene | TTN |
Other symbol(s) | CMPD4 |
Main clinical features | early onset leading to precocious heart failure |
Genetic determination | |
Related entries | cardiomyopathy familial hypertrophic |
Function/system disorder | cardiovascular |
Type | disease |
Gene product |
Name | titin |