| Label | Id | |
|---|---|---|
| deficiency, Vitamin | http://purl.obolibrary.org/obo/MONDO_0024298 | |
| chromosome 5q12 deletion syndrome | 14298 | |
| syndromes, neuroectodermal dysplasia | 42983 | |
| disease of stomach | 4298 | |
| Westphal variant of Huntington's disease | 42980 | |
| complete absence of bile and pancreatic ducts | C564298 | |
| stomach disease or disorder | 4298 | |
| disorder of stomach | 4298 | |
| GATA2 deficiency/MonoMac syndrome | http://purl.obolibrary.org/obo/MONDO_0042982 | |
| valvular aortic stenosis | 42981 | |
| PDE4D haploinsufficiency syndrome | 14298 | |
| neuroectodermal dysplasia syndrome | 42983 | |
| neuroectodermal dysplasia syndromes | 42983 | |
| stenosed aortic valve | 42981 | |
| HD- Westphal variant | 42980 |