All terms in MONDO
| Label | Id | Description |
|---|---|---|
| ptosis, hereditary congenital 2 | MONDO_0010280 | |
| mycobacterium tuberculosis, susceptibility to, X-linked | MONDO_0010282 | |
| Danon disease | MONDO_0010281 | |
| Armfield syndrome | MONDO_0010284 | |
| gonadal dysgenesis | MONDO_0001967 | |
| GOMBO syndrome | MONDO_0009298 | |
| FG syndrome 2 | MONDO_0010297 | |
| immunodeficiency 61 | MONDO_0010296 | |
| hypoxanthine guanine phosphoribosyltransferase partial deficiency | MONDO_0010299 | |
| obsolete androgen insensitivity syndrome due to coactivator deficiency | MONDO_0010291 | |
| goiter, multinodular 2 | MONDO_0010290 | |
| ectodermal dysplasia and immune deficiency | MONDO_0010293 | |
| Uruguay Faciocardiomusculoskeletal syndrome | MONDO_0010292 | |
| anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome | MONDO_0010295 | |
| X-linked severe congenital neutropenia | MONDO_0010294 | |
| MONDO_0022266 | MONDO_0022266 | |
| MONDO_0022267 | MONDO_0022267 | |
| obsolete congenital hepatic fibrosis | MONDO_0022263 | |
| vascular disorder of penis | MONDO_0022293 | |
| Bartter disease type 4B | MONDO_0000909 |