| Label | Id | |
|---|---|---|
| MLC2B | 0013491 | |
| PNCA4 | 0013685 | |
| LWNH | 0013688 | |
| PTHSL2 | 0013690 | |
| Feingold syndrome 2 | 0013691 | |
| PNLIPD | 0013700 | |
| C4AD | 0013721 | |
| EMARDD | 0013731 | |
| ACTFS | 0013733 | |
| RHFCA | 0013740 | |
| VSD1 | 0013746 | |
| Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive | 0013753 | |
| CMM8 | 0013759 | |
| ISQMR | 0013760 | |
| FCAS3 | 0013766 |