|
Genes linked to monogenic diseases with associated cardiovascular defects |
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| Gene name |
OMIM reference for the disease |
Identification of the responsible gene |
|
|
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| TG132 |
160781 (heart formation defect) |
+ |
| TG154 |
191044 (cardiomyopathy) |
+ |
| TG131 |
160760 (cardiomyopathy) |
+ |
| TG13 |
191045 (cardiomyopathy) |
+ |
| TG78 |
150000 (enzyme deficiency) |
+ |
| TG4_183 |
601628 (bleeding disorder) |
- |
| Modifier of von Willebrand factor |
||
|
Gene names are from Figure 1. The cognate diseases and their references in OMIM are noted. +, Previously known relationship; -, unknown relationship (candidate gene). | ||
Mégy et al. Genome Biology 2002 3:research0074.1 doi:10.1186/gb-2002-3-12-research0074 |
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