All terms in MONDO
| Label | Id | Description |
|---|---|---|
| FG syndrome 5 | MONDO_0010366 | |
| nystagmus 5, congenital, X-linked | MONDO_0010369 | |
| obsolete immunodeficiency without anhidrotic ectodermal dysplasia | MONDO_0010368 | |
| congenital absence of septum pellucidum | MONDO_0022349 | |
| benign Leydig cell tumor | MONDO_0036990 | |
| intellectual disability, X-linked 30 | MONDO_0010361 | |
| parkinson disease 12 | MONDO_0010360 | |
| Dent disease type 2 | MONDO_0010359 | |
| Dent disease | MONDO_0015612 | |
| Rotor syndrome | MONDO_0009379 | |
| hyper-beta-alaninemia | MONDO_0009378 | |
| hyperammonemia due to N-acetylglutamate synthase deficiency | MONDO_0009377 | |
| carbamoyl phosphate synthetase I deficiency disease | MONDO_0009376 | |
| hymen, imperforate | MONDO_0009375 | |
| hyperleucine-Isoleucinemia | MONDO_0009385 | |
| retinitis pigmentosa 34 | MONDO_0010374 | |
| Leydig cell hypoplasia, type 1 | MONDO_0009384 | |
| Leydig cell hypoplasia | MONDO_0019155 | |
| premature ovarian failure 2B | MONDO_0010373 | |
| transient familial neonatal hyperbilirubinemia | MONDO_0009383 |