| Label | Id | |
|---|---|---|
| EPIDERMAL NEVUS WITH UROTHELIAL CANCER, SOMATIC | 190020 | |
| THYROID CARCINOMA, FOLLICULAR, SOMATIC | 190020 | |
| p21 | 190020 | |
| COSTELLO SYNDROME | 190020 | |
| NEVUS SEBACEOUS, SOMATIC | 190020 | |
| TRANSFORMATION GENE: ONCOGENE HAMSV | 190020 | |
| BEARE-STEVENSON CUTIS GYRATA SYNDROME | 123790 | |
| CUTIS GYRATA SYNDROME OF BEARE AND STEVENSON | 123790 | |
| BEARE-STEVENSON SYNDROME | 123790 | |
| BSTVS | 123790 | |
| COACH SYNDROME 1 | 216360 | |
| CEREBELLAR VERMIS HYPO/APLASIA, OLIGOPHRENIA, CONGENITAL ATAXIA, OCULAR COLOBOMA, AND HEPATIC FIBROSIS | 216360 | |
| JOUBERT SYNDROME WITH CONGENITAL HEPATIC FIBROSIS | 216360 | |
| COACH1 | 216360 | |
| COACH SYNDROME | 216360 |