| Label | Id | |
|---|---|---|
| SPTAN1 early infantile epileptic encephalopathy | 13277 | |
| 16p13.3 microduplication syndrome | 13273 | |
| long QT syndrome caused by mutation in KCNJ5 | 13279 | |
| long QT syndrome 13 | 13279 | |
| long QT syndrome 13; LQT13 | http://purl.obolibrary.org/obo/MONDO_0013279 | |
| long QT syndrome type 13 | 13279 | |
| retinitis pigmentosa type 51 | 13274 | |
| lymphedema, hereditary, type 1C | 13278 | |
| carcinoma of the urethra | 21327 | |
| carcinoma of urethra | 21327 | |
| frontonasal dysplasia type 3 | 13271 | |
| pelvic muscle wasting | 1327 |