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