All terms in MONDO
| Label | Id | Description |
|---|---|---|
| obsolete inherited renal tumor | MONDO_0015963 | |
| nephronophthisis 11 | MONDO_0013302 | |
| commissural facial cleft | MONDO_0013300 | |
| obsolete rare genetic hypothalamic or pituitary disease | MONDO_0015968 | |
| autosomal dominant nonsyndromic hearing loss 51 | MONDO_0013305 | |
| combined oxidative phosphorylation defect type 7 | MONDO_0013306 | |
| late latent syphilis | MONDO_0040923 | |
| obsolete hereditary eye tumor | MONDO_0015966 | |
| autoimmune disease, susceptibility to, 6 | MONDO_0013303 | |
| latent early syphilis | MONDO_0040922 | |
| von Willebrand disease 2 | MONDO_0013304 | |
| obsolete rare genetic refraction anomaly | MONDO_0015965 | |
| obsolete genetic polycythemia | MONDO_0027929 | |
| bladder lateral wall cancer | MONDO_0001319 | |
| phlyctenulosis | MONDO_0001317 | |
| latent yaws | MONDO_0040925 | |
| intrahepatic bile duct cystadenoma | MONDO_0003979 | |
| obsolete rare genetic developmental defect during embryogenesis | MONDO_0015960 | |
| obsolete MONDO:0003986 | MONDO_0003986 | |
| infant gynecomastia | MONDO_0001323 |