All terms in MONDO
| Label | Id | Description |
|---|---|---|
| isolated congenital syngnathia | MONDO_0015409 | |
| lipoadenoma | MONDO_0003431 | |
| diffuse lymphatic malformation | MONDO_0015408 | |
| lethal recessive chondrodysplasia | MONDO_0015425 | |
| lethal chondrodysplasia, Moerman type | MONDO_0015424 | |
| obsolete anaplastic thyroid carcinoma | MONDO_0015423 | |
| orofaciodigital syndrome type 13 | MONDO_0015422 | |
| choroideremia-hypopituitarism syndrome | MONDO_0015429 | |
| choroidal atrophy-alopecia syndrome | MONDO_0015428 | |
| orofaciodigital syndrome type 12 | MONDO_0015421 | |
| clear cell hidradenoma | MONDO_0003447 | |
| obsolete syringocystadenoma papilliferum | MONDO_0003449 | |
| intrahepatic bile duct adenoma | MONDO_0003444 | |
| papillary hidradenoma | MONDO_0003446 | |
| obsolete bladder flat intraepithelial lesion | MONDO_0003440 | |
| midline cervical cleft | MONDO_0015419 | |
| ring chromosome 20 | MONDO_0015436 | |
| ring chromosome 19 | MONDO_0015435 | |
| ring chromosome 18 | MONDO_0015434 | |
| ring chromosome 17 | MONDO_0015433 |