| Label | Id | |
|---|---|---|
| ARMD11 | 12767 | |
| CPVT2 | 12762 | |
| CVPT2 | 12762 | |
| EIG5 | 12760 | |
| HPC11 | 12768 | |
| HPC14 | 12769 | |
| LMPH1B | 12765 | |
| SPG37 | 12766 | |
| shock | D012769 | |
| 3q29 microduplication | 12761 | |
| trisomy 3q29 | 12761 | |
| RIDDLE syndrome | 12764 | |
| RNF168 deficiency | 12764 | |
| orofacial cleft 2; OFC2 | http://purl.obolibrary.org/obo/MONDO_0011276 | |
| spastic paraplegia 37, autosomal dominant | 12766 |