All terms in MONDO
| Label | Id | Description |
|---|---|---|
| inherited sideroblastic anemia | MONDO_0020099 | |
| flat face-microstomia-ear anomaly syndrome | MONDO_0008421 | |
| spastic paraplegia-epilepsy-intellectual disability syndrome | MONDO_0008439 | |
| hereditary spastic paraplegia 4 | MONDO_0008438 | |
| pure or complex autosomal dominant spastic paraplegia | MONDO_0017914 | |
| hereditary spastic paraplegia 3A | MONDO_0008437 | |
| Sneddon syndrome | MONDO_0008436 | |
| Somatomedin, embryonic | MONDO_0008435 | |
| Smith-Magenis syndrome | MONDO_0008434 | |
| small cell lung carcinoma | MONDO_0008433 | |
| obsolete ketone compounds, ability to smell | MONDO_0008432 | |
| slipped femoral capital epiphyses | MONDO_0008431 | |
| skeletal dysplasia with delayed epiphyseal and carpal bone ossification | MONDO_0008430 | |
| polyp of ethmoidal sinus | MONDO_0021418 | |
| polyp of vocal cord | MONDO_0021420 | |
| laryngeal disorder | MONDO_0004382 | |
| obsolete carcinoid tumors, intestina | MONDO_0021421 | |
| MONDO_0021422 | MONDO_0021422 | |
| spina bifida | MONDO_0008449 | |
| spinal cord disorder | MONDO_0002545 |