All terms in MONDO
| Label | Id | Description |
|---|---|---|
| FRAXF syndrome | MONDO_0015084 | |
| proteasome-associated autoinflammatory syndrome 3 | MONDO_0054699 | |
| proteasome-associated autoinflammatory syndrome 1 | MONDO_0054698 | |
| immunodeficiency 11b with atopic dermatitis | MONDO_0054697 | |
| immunodeficiency 53 | MONDO_0054696 | |
| alopecia antibody deficiency | MONDO_0015082 | |
| obsolete neuroendocrine tumor with other location | MONDO_0015081 | |
| obsolete thymic tumor | MONDO_0015080 | |
| obsolete situs inversus totalis | MONDO_0015098 | |
| aortic valve dysplasia | MONDO_0015097 | |
| familial hypofibrinogenemia | MONDO_0015096 | |
| Peters anomaly-cataract syndrome | MONDO_0015095 | |
| ovarian dysgenesis 5 | MONDO_0054666 | |
| pituitary adenoma 3, multiple types | MONDO_0054665 | |
| unilateral hemispheric polymicrogyria | MONDO_0015099 | |
| subependymal nodular heterotopia | MONDO_0015094 | |
| sub-cortical nodular heterotopia | MONDO_0015093 | |
| cleft hard palate | MONDO_0015092 | |
| high-grade B-cell lymphoma double-hit/triple-hit | MONDO_0850426 | |
| combined oxidative phosphorylation deficiency 33 | MONDO_0054677 |

