All terms in MONDO
| Label | Id | Description |
|---|---|---|
| discrimination, Two-point, reduction 1N | MONDO_0007460 | |
| dysphagia lusoria | MONDO_0020418 | |
| aortic arch defects | MONDO_0015236 | |
| right aortic arch | MONDO_0020417 | |
| Neuhauser anomaly | MONDO_0020416 | |
| lissencephaly type 3-familial fetal akinesia sequence syndrome | MONDO_0019449 | |
| Kommerell diverticulum | MONDO_0020415 | |
| benign adult familial myoclonic epilepsy | MONDO_0019448 | |
| persistent fifth aortic arch | MONDO_0020414 | |
| encircling double aortic arch | MONDO_0020413 | |
| arthrogryposis-ectodermal dysplasia-other anomalies syndrome | MONDO_0044406 | |
| trichofolliculoma | MONDO_0019445 | |
| trichinellosis | MONDO_0019444 | |
| ATTRV122I amyloidosis | MONDO_0019441 | |
| familial amyloid neuropathy | MONDO_0007100 | |
| wild type ABeta2M amyloidosis | MONDO_0019440 | |
| obsolete congenital toxoplasmosis | MONDO_0019442 | |
| double nail for fifth toe | MONDO_0007469 | |
| DNA, low-repetitive sequences of | MONDO_0007467 | |
| stenosis or atrophy of the coronary ostium | MONDO_0020423 |