All terms in MONDO
| Label | Id | Description |
|---|---|---|
| rhizomelic syndrome, Urbach type | MONDO_0009996 | |
| chronic myelomonocytic leukemia | MONDO_0020311 | |
| van der Woude syndrome 1 | MONDO_0007333 | |
| Brody myopathy | MONDO_0010977 | |
| autosomal dominant popliteal pterygium syndrome | MONDO_0007334 | |
| obsolete rheumatic fever-related antigen | MONDO_0009995 | |
| alveolar rhabdomyosarcoma | MONDO_0009994 | |
| obsolete cleft chin | MONDO_0007331 | |
| Timothy syndrome | MONDO_0010979 | |
| split-hand/foot malformation with long bone deficiency 1 | MONDO_0007332 | |
| myoglobinuria, acute recurrent, autosomal recessive | MONDO_0009992 | |
| congenital pseudoarthrosis of clavicle | MONDO_0007330 | |
| obsolete Rh deficiency syndrome | MONDO_0009991 | |
| obsolete Cd4/CD8 T-cell ratio | MONDO_0010990 | |
| Ayme-Gripp syndrome | MONDO_0010992 | |
| laterality defects, autosomal dominant | MONDO_0010991 | |
| macrocystic lymphatic malformation | MONDO_0019328 | |
| obsolete micromelic dwarfism, Fryns type | MONDO_0010994 | |
| phakomatosis spilorosea | MONDO_0019327 | |
| phakomatosis pigmentovascularis | MONDO_0017318 |