All terms in MONDO
| Label | Id | Description |
|---|---|---|
| neurodegeneration with brain iron accumulation 4 | MONDO_0013674 | |
| autosomal dominant hypocalcemia 1 | MONDO_0011013 | |
| sclerosteosis 2 | MONDO_0013679 | |
| type 1 diabetes mellitus 11 | MONDO_0011016 | |
| cataract 24 | MONDO_0011015 | |
| brachyolmia-amelogenesis imperfecta syndrome | MONDO_0011018 | |
| Emery-Dreifuss muscular dystrophy 7, autosomal dominant | MONDO_0013677 | |
| EDICT syndrome | MONDO_0013678 | |
| Naxos disease | MONDO_0011017 | |
| hydatidiform mole, recurrent, 2 | MONDO_0013671 | |
| chromosome 15q25 deletion syndrome | MONDO_0013672 | |
| Matthew-Wood syndrome | MONDO_0011010 | |
| myopia, high, with cataract and vitreoretinal degeneration | MONDO_0013670 | |
| obsolete Ehlers-Danlos syndrome | MONDO_0001696 | |
| double discordia | MONDO_0023002 | |
| senile ectropion | MONDO_0001695 | |
| double fingernail of fifth finger | MONDO_0023003 | |
| diffuse interstitial keratitis | MONDO_0001694 | |
| double uterus-hemivagina-renal agenesis | MONDO_0023005 | |
| limbal stem cell deficiency | MONDO_0025667 |