All terms in MONDO
| Label | Id | Description |
|---|---|---|
| Charcot-Marie-Tooth disease axonal type 2U | MONDO_0014566 | |
| cataract 43 | MONDO_0014565 | |
| congenital bile acid synthesis defect 5 | MONDO_0014564 | |
| lethal congenital contracture syndrome 7 | MONDO_0014569 | |
| hypomyelination neuropathy-arthrogryposis syndrome | MONDO_0017049 | |
| hereditary spastic paraplegia 73 | MONDO_0014568 | |
| autosomal dominant pure spastic paraplegia | MONDO_0015088 | |
| mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency | MONDO_0014563 | |
| Leigh syndrome with leukodystrophy | MONDO_0016815 | |
| neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome | MONDO_0014562 | |
| 3-methylglutaconic aciduria, type VIIB | MONDO_0014561 | |
| 3-methylglutaconic aciduria | MONDO_0017359 | |
| amelogenesis imperfecta type 1F | MONDO_0014560 | |
| obsolete thymoma type AB | MONDO_0002589 | |
| breast fibrocystic disease | MONDO_0005219 | |
| encapsulated thymoma | MONDO_0002587 | |
| subacute leukemia | MONDO_0002582 | |
| mucinous ovarian cystadenoma | MONDO_0002583 | |
| obsolete syringomyelia | MONDO_0002584 | |
| orbit sarcoma | MONDO_0004943 |