| Label | Id | |
|---|---|---|
| CACP | 8828 | |
| PTORCH2 | 18828 | |
| USP18 deficiency | 18828 | |
| UPS18 deficiency | 18828.0 | |
| CACP syndrome | 8828 | |
| Jacobs syndrome | 8828 | |
| PAC syndrome | 8828 | |
| arthropathy-camptodactyly syndrome | 8828 | |
| camptodactyly-arthropathy-coxa-vara-pericarditis syndrome | 8828 | |
| camptodactyly-arthropathy-pericarditis syndrome | 8828 | |
| pericarditis-arthropathy-camptodactyly syndrome | 8828 | |
| Cortico-basal degeneration | D000088282 | |
| hypertrophic synovitis, congenital familial | 8828 | |
| pseudo-TORCH syndrome 2; PTORCH2 | http://purl.obolibrary.org/obo/MONDO_0018828 | |
| pseudo-TORCH syndrome 2 | 18828 |