All terms in MONDO
| Label | Id | Description |
|---|---|---|
| primary immunodeficiency due to a genetic defect in innate immunity | MONDO_0015135 | |
| viral hemorrhagic fever | MONDO_0018087 | |
| hemorrhagic fever | MONDO_0600002 | |
| ventricular septal defect | MONDO_0002070 | |
| genetic cardiac anomaly | MONDO_0017131 | |
| Uhl anomaly | MONDO_0018084 | |
| cardiomyopathy | MONDO_0004994 | |
| transient tyrosinemia of the newborn | MONDO_0018083 | |
| tyrosinemia | MONDO_0004741 | |
| ulerythema ophryogenesis | MONDO_0018086 | |
| umbilical cord ulceration-intestinal atresia syndrome | MONDO_0018085 | |
| syndromic intestinal malformation | MONDO_0015212 | |
| obsolete rare germ cell tumor | MONDO_0018080 | |
| aorto-ventricular tunnel | MONDO_0018082 | |
| ascending aorta anomaly | MONDO_0020293 | |
| hemorrhagic fever-renal syndrome | MONDO_0018081 | |
| developmental and epileptic encephalopathy 106 | MONDO_0031052 | |
| dyskeratosis congenita, digenic | MONDO_0031057 | |
| developmental and epileptic encephalopathy 107 | MONDO_0031055 | |
| obsolete Whipple disease | MONDO_0018099 |