| Label | Id | |
|---|---|---|
| DRS1 | 0024455 | |
| autosomal dominant Robinow syndrome caused by mutation in WNT5A | 0024455 | |
| Robinow syndrome, autosomal dominant 1 | 0024455 | |
| WNT5A autosomal dominant Robinow syndrome | 0024455 | |
| dysostosis acral with facial and genital abnormalities | 0024455 |