All terms in MONDO
| Label | Id | Description |
|---|---|---|
| obsolete brain calcification, Rajab type | MONDO_0013346 | |
| C1Q deficiency | MONDO_0013343 | |
| migraine, with or without aura, susceptibility to, 13 | MONDO_0013344 | |
| ALG11-congenital disorder of glycosylation | MONDO_0013349 | |
| obsolete gastric cancer | MONDO_0013347 | |
| cone-rod dystrophy 15 | MONDO_0013348 | |
| methylmalonic acidemia due to transcobalamin receptor defect | MONDO_0013341 | |
| hereditary spastic paraplegia 48 | MONDO_0013342 | |
| Parkinson disease 5, autosomal dominant, susceptibility to | MONDO_0013340 | |
| chronic congestive splenomegaly | MONDO_0001367 | |
| congestive splenomegaly | MONDO_0037251 | |
| splenic sequestration | MONDO_0001366 | |
| necrosis of ear ossicle | MONDO_0001365 | |
| regular astigmatism | MONDO_0001364 | |
| astigmatism | MONDO_0011284 | |
| chronic laryngitis | MONDO_0001369 | |
| phthisical cornea | MONDO_0001368 | |
| blind hypertensive eye | MONDO_0001363 | |
| obsolete leukocoria | MONDO_0001362 | |
| spontaneous ocular nystagmus | MONDO_0001361 |