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| GENATLAS PHENOTYPE |
| last update : 07-06-2011 |
| Symbol | CMD1R |
| Location | 15q14 |
| Name | cardiomyopathy, dilated 1R |
| Other name(s) | cardiomyopathy, dilated 1A, with conduction defect |
| Corresponding gene | ACTC1 |
| Other symbol(s) | CMD1ACT |
| Main clinical features | idiopathic dilated cardiomyopathy |
| Genetic determination | autosomal dominant |
| Related entries | including cardiomyopathy familial hypertrophic, and idiopathic restrictive cardiomyopathy in childhood (PMID: 18467357) |
| Function/system disorder | cardiovascular |
| neuromuscular | |
| Type | disease |
| Gene product |
| Name | actin, alpha, cardiac (ACTC) |
| Remark(s) |