All terms in MONDO
| Label | Id | Description |
|---|---|---|
| dilated cardiomyopathy 1U | MONDO_0013371 | |
| supernumerary der(22)t(8;22) syndrome | MONDO_0013374 | |
| Klippel-Feil syndrome 3, autosomal dominant | MONDO_0013375 | |
| dilated cardiomyopathy 1V | MONDO_0013373 | |
| ureter leiomyoma | MONDO_0001399 | |
| Nairobi sheep disease | MONDO_0025369 | |
| monocular exotropia | MONDO_0001392 | |
| exotropia | MONDO_0001286 | |
| indeterminate leprosy | MONDO_0001391 | |
| transient refractive change | MONDO_0001390 | |
| abnormal threshold of rods | MONDO_0001396 | |
| macular keratitis | MONDO_0001395 | |
| chronic erythremia | MONDO_0001394 | |
| peripheral focal chorioretinitis | MONDO_0001393 | |
| developmental and epileptic encephalopathy, 12 | MONDO_0013389 | |
| developmental and epileptic encephalopathy, 7 | MONDO_0013387 | |
| developmental and epileptic encephalopathy, 11 | MONDO_0013388 | |
| neuropathy, hereditary sensory, type 1D | MONDO_0013381 | |
| progressive demyelinating neuropathy with bilateral striatal necrosis | MONDO_0013382 | |
| LEOPARD syndrome 3 | MONDO_0013380 |