| Label | Id | |
|---|---|---|
| CMH20 | 13477 | |
| hypertrophic cardiomyopathy 20 | 13477 | |
| hypertrophic cardiomyopathy type 20 | 13477 | |
| hypertrophic cardiomyopathy caused by mutation in NEXN | 13477 | |
| cardiomyopathy familial hypertrophic 20 | 13477 | |
| cardiomyopathy, familial hypertrophic, 20 | 13477 | |
| cardiomyopathy, familial hypertrophic, 20; CMH20 | http://purl.obolibrary.org/obo/MONDO_0013477 | |
| cardiomyopathy, familial hypertrophic, type 20 | 13477 | |
| NEXN hypertrophic cardiomyopathy | 13477 |