All terms in MONDO
| Label | Id | Description |
|---|---|---|
| hearing loss, autosomal recessive 110 | MONDO_0054860 | |
| cardiac anomalies-heterotaxy syndrome | MONDO_0015296 | |
| intractable diarrhea-choanal atresia-eye anomalies syndrome | MONDO_0015295 | |
| nephrogenic systemic fibrosis | MONDO_0015294 | |
| segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome | MONDO_0015293 | |
| PTEN hamartoma tumor syndrome | MONDO_0017623 | |
| Asherman syndrome | MONDO_0015299 | |
| premature ovarian failure 15 | MONDO_0054862 | |
| pellucid marginal degeneration | MONDO_0015298 | |
| intellectual disability, autosomal recessive 63 | MONDO_0054861 | |
| obsolete microcephaly-digital anomalies-intellectual disability syndrome | MONDO_0015297 | |
| endotheliitis | MONDO_0015292 | |
| stromal keratitis | MONDO_0015291 | |
| neurotrophic keratopathy | MONDO_0015290 | |
| meconium ileus | MONDO_0054868 | |
| paraomphalocele | MONDO_0054867 | |
| sudden arrhythmia death syndrome | MONDO_0054866 | |
| nondystrophic myotonia | MONDO_0054869 | |
| obsolete Churg-Strauss syndrome | MONDO_0005703 | |
| obsolete chromoblastomycosis | MONDO_0005702 |