All terms in MONDO
| Label | Id | Description |
|---|---|---|
| partial deletion of the long arm of chromosome 13 | MONDO_0016911 | |
| generalized eruptive keratoacanthoma | MONDO_0018471 | |
| keratoacanthoma | MONDO_0002527 | |
| renal agenesis | MONDO_0018470 | |
| inherited kidney disorder | MONDO_0100191 | |
| Potter sequence | MONDO_0001558 | |
| hamartoma | MONDO_0006499 | |
| cerebral palsy | MONDO_0006497 | |
| cerebral cortex disorder | MONDO_0044996 | |
| palsy | MONDO_0006496 | |
| adenomatous colon polyp | MONDO_0006498 | |
| polyp of colon | MONDO_0021400 | |
| colon adenoma | MONDO_0000527 | |
| obsolete marginal zone B-cell lymphoma | MONDO_0006495 | |
| central nervous system disorder | MONDO_0002602 | |
| Warthin tumor | MONDO_0006493 | |
| digestive system adenoma | MONDO_0006180 | |
| benign neoplasm of salivary gland | MONDO_0021460 | |
| obsolete thyroid disease | MONDO_0006494 | |
| obsolete rare genetic odontal or periodontal disorder | MONDO_0018488 |