All terms in MONDO
| Label | Id | Description |
|---|---|---|
| obsolete Heimler syndrome | MONDO_0100229 | |
| fatty acyl-CoA reductase 1 dysregulation | MONDO_0100230 | |
| psoriatic arthritis, susceptibility to, 1 | MONDO_0100231 | |
| psoriatic arthritis, susceptibility to | MONDO_0100232 | |
| psoriatic arthritis | MONDO_0011849 | |
| long COVID-19 | MONDO_0100233 | |
| paroxysmal familial ventricular fibrillation | MONDO_0100234 | |
| ventricular fibrillation | MONDO_0000190 | |
| FOXC1-related anterior segment dysgenesis | MONDO_0100235 | |
| iridogoniodysgenesis | MONDO_0011119 | |
| LTBP2-related ocular dysgenesis | MONDO_0100236 | |
| cutis laxa | MONDO_0016175 | |
| inherited Fanconi renotubular syndrome | MONDO_0100238 | |
| Fanconi renotubular syndrome | MONDO_0001083 | |
| inherited hypertrophic pyloric stenosis | MONDO_0100239 | |
| hypertrophic pyloric stenosis | MONDO_0001560 | |
| thrombophilia | MONDO_0002305 | |
| glioma susceptibility | MONDO_0100242 | |
| obsolete inherited paroxysmal nocturnal hemoglobinuria | MONDO_0100243 | |
| hemoglobinuria | MONDO_0003656 |