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| References | OMIM | Gene | GeneReviews | HGMD | HGNC |
| GENATLAS PHENOTYPE |
| last update : 20/03/2006 |
| Symbol | CMH2 |
| Location | 1q32 |
| HGNC id | 2114 |
| Name | cardiomyopathy, familial, hypertrophic, 2 |
| Corresponding gene | TNNT2 |
| Genetic determination | autosomal dominant |
| Related entries | including dilated form |
| Function/system disorder | cardiovascular |
| neuromuscular | |
| Type | disease |
| Gene product |
| Name | troponin T2,cardiac muscle (TNNT2) |