All terms in MONDO
| Label | Id | Description |
|---|---|---|
| partial duplication of the short arm of chromosome 7 | MONDO_0016944 | |
| drug-induced lupus erythematosus | MONDO_0016474 | |
| Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 | MONDO_0016475 | |
| Beckwith-Wiedemann syndrome due to CDKN1C mutation | MONDO_0016476 | |
| Beckwith-Wiedemann syndrome due to 11p15 microdeletion | MONDO_0016477 | |
| Ehlers-Danlos/osteogenesis imperfecta syndrome | MONDO_0016470 | |
| osteogenesis imperfecta | MONDO_0019019 | |
| pachyonychia congenita | MONDO_0016471 | |
| focal palmoplantar keratoderma | MONDO_0017672 | |
| dracunculiasis | MONDO_0016472 | |
| Rhabditida infectious disease | MONDO_0005943 | |
| familial rhabdoid tumor | MONDO_0016473 | |
| rhabdoid tumor | MONDO_0002728 | |
| lung hilum carcinoma | MONDO_0004499 | |
| lung hilum cancer | MONDO_0004332 | |
| inflammation of heart layer | MONDO_0024636 | |
| myotonic cataract | MONDO_0004495 | |
| myotonic dystrophy | MONDO_0016107 | |
| sacral spinal canal and spinal cord meningioma | MONDO_0004498 | |
| intraspinal meningioma | MONDO_0001279 |