All terms in MONDO
| Label | Id | Description |
|---|---|---|
| chromosome 2p12-p11.2 deletion syndrome | MONDO_0013309 | |
| malignant breast myoepithelioma | MONDO_0003990 | |
| myopathy, lactic acidosis, and sideroblastic anemia 2 | MONDO_0013307 | |
| villoglandular endometrial endometrioid adenocarcinoma | MONDO_0003991 | |
| CBL-related disorder | MONDO_0013308 | |
| obsolete rare genetic thyroid disease | MONDO_0015969 | |
| presbyopia | MONDO_0001330 | |
| cranioectodermal dysplasia 2 | MONDO_0013323 | |
| bone dysplasia, Azouz type | MONDO_0015985 | |
| lymphedema-posterior choanal atresia syndrome | MONDO_0013324 | |
| obsolete rare genetic immune disease | MONDO_0015984 | |
| forsythe-wakeling syndrome | MONDO_0013321 | |
| epilepsy, familial adult myoclonic, 3 | MONDO_0013322 | |
| obsolete rare genetic syndromic intellectual disability | MONDO_0015983 | |
| primary hyperoxaluria type 3 | MONDO_0013327 | |
| retinitis pigmentosa 58 | MONDO_0013328 | |
| obsolete congenital valvular dysplasia | MONDO_0015989 | |
| COG5-congenital disorder of glycosylation | MONDO_0013325 | |
| Senior-Loken syndrome 7 | MONDO_0013326 | |
| scimitar syndrome | MONDO_0015987 |