eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | 1p36 deletion syndrome |
| Comorbidity | C0878544|cardiomyopathy |
| Sentences | 2 |
| PubMedID- 25035420 | Prdm16 was recently identified as a causative gene of left ventricular non-compaction and dilated cardiomyopathy in 1p36 deletion syndrome, which is characterized by heart failure, arrhythmia and sudden cardiac death. |
| PubMedID- 24387995 | Loss of prdm16 is unlikely to cause cardiomyopathy in 1p36 deletion syndrome. |
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