All terms in MONDO
| Label | Id | Description |
|---|---|---|
| Leber congenital amaurosis | MONDO_0018998 | |
| RPE65-related recessive retinopathy | MONDO_0100368 | |
| Leber congenital amaurosis 1 | MONDO_0008764 | |
| GUCY2D-related recessive retinopathy | MONDO_0100453 | |
| obsolete Bartholin gland squamous cell carcinoma | MONDO_0006101 | |
| basaloid carcinoma | MONDO_0006102 | |
| Alstrom syndrome | MONDO_0008763 | |
| ciliopathy | MONDO_0005308 | |
| autosomal recessive Alport syndrome | MONDO_0008762 | |
| Alport syndrome | MONDO_0018965 | |
| obsolete Bartholin gland carcinoma | MONDO_0006100 | |
| obsolete alpha-2-deficient collagen disease | MONDO_0008761 | |
| beta-ketothiolase deficiency | MONDO_0008760 | |
| inborn disorder of ketolysis | MONDO_0019229 | |
| classic organic aciduria | MONDO_0019215 | |
| vulvodynia | MONDO_0021722 | |
| female reproductive system disorder | MONDO_0002263 | |
| vaginismus | MONDO_0021723 | |
| vaginal disorder | MONDO_0001433 | |
| obsolete Abderhalden-Kaufmann-Lignac syndrome | MONDO_0021725 |