All terms in MONDO
| Label | Id | Description |
|---|---|---|
| Blau syndrome | MONDO_0008523 | |
| sarcoidosis | MONDO_0019338 | |
| synovial chondromatosis, familial, with dwarfism | MONDO_0008522 | |
| brachydactyly-elbow wrist dysplasia syndrome | MONDO_0008520 | |
| obsolete distal arthrogryposis type 10 | MONDO_0008539 | |
| temporal arteritis | MONDO_0008538 | |
| predominantly large-vessel vasculitis | MONDO_0015488 | |
| central nervous system vasculitis | MONDO_0003346 | |
| granulomatous angiitis | MONDO_0002341 | |
| telecanthus | MONDO_0008537 | |
| canthal anomaly | MONDO_0020163 | |
| temperature-sensitive lethal mutation | MONDO_0008536 | |
| telangiectasia, hereditary hemorrhagic, type 1 | MONDO_0008535 | |
| hereditary hemorrhagic telangiectasia | MONDO_0019180 | |
| generalized essential telangiectasia | MONDO_0008534 | |
| skin vascular disease | MONDO_0019293 | |
| teeth, supernumerary | MONDO_0008533 | |
| teeth present at birth | MONDO_0008532 | |
| obsolete T-complex locus TCP10B | MONDO_0008531 | |
| teeth, odd shapes of | MONDO_0008530 |