All terms in MONDO
| Label | Id | Description |
|---|---|---|
| chromosome 20 trisomy | MONDO_0022757 | |
| relapsing polychondritis | MONDO_0019125 | |
| chromosome 22, monosome mosaic | MONDO_0022758 | |
| mullerian aplasia | MONDO_0019128 | |
| uterovaginal malformation | MONDO_0015828 | |
| idiopathic acute eosinophilic pneumonia | MONDO_0019122 | |
| idiopathic hypereosinophilic syndrome | MONDO_0011895 | |
| idiopathic eosinophilic pneumonia | MONDO_0015927 | |
| pneumocystosis | MONDO_0019121 | |
| Pneumocystis infectious disease | MONDO_0005923 | |
| MERRF syndrome | MONDO_0010790 | |
| microscopic polyangiitis | MONDO_0019124 | |
| continuous spikes and waves during sleep | MONDO_0019123 | |
| chromosome 3 duplication syndrome | MONDO_0022761 | |
| pili bifurcati | MONDO_0019120 | |
| chronic demyelinizing neuropathy with IgM monoclonal | MONDO_0022765 | |
| appendicitis, proneness to | MONDO_0007148 | |
| obsolete rare constitutional hemolytic anemia due to an enzyme disorder | MONDO_0020104 | |
| obsolete arbitrary restriction polymorphism 1 | MONDO_0007149 | |
| obsolete constitutional hemolytic anemia due to acanthocytosis | MONDO_0020103 |