All terms in MONDO
| Label | Id | Description |
|---|---|---|
| palmoplantar keratoderma-sclerodactyly syndrome | MONDO_0008416 | |
| obsolete Scholte syndrome | MONDO_0008415 | |
| schizophrenia 1 | MONDO_0008414 | |
| obsolete schizophrenia | MONDO_0008413 | |
| intestinal schistosomiasis | MONDO_0008412 | |
| intestinal helminthiasis | MONDO_0024271 | |
| ulnar-mammary syndrome | MONDO_0008411 | |
| Scheuermann disease | MONDO_0008410 | |
| Singleton-Merten dysplasia | MONDO_0008429 | |
| combined pituitary hormone deficiencies, genetic form | MONDO_0013099 | |
| sister chromatid exchange, frequency of | MONDO_0008427 | |
| Shprintzen-Goldberg syndrome | MONDO_0008426 | |
| Marfan and Marfan-related disorder | MONDO_0017310 | |
| polyp of external auditory canal | MONDO_0021402 | |
| external ear neoplasm | MONDO_0021235 | |
| omphalocele syndrome, Shprintzen-Goldberg type | MONDO_0008425 | |
| sella turcica, bridged | MONDO_0008424 | |
| sinus node disease and myopia | MONDO_0008423 | |
| familial sick sinus syndrome | MONDO_0012061 | |
| autosomal dominant sideroblastic anemia | MONDO_0008422 |