DOID:1270 - hereditary hemorrhagic telangiectasia
Disease Ontology Definition:A vascular disease characterized by the presence of multiple arteriovenous malformations that lack intervening capillaries and result in direct connections between arteries and veins.
Synonyms: Osler hemorrhagic telangiectasia syndrome, Osler-Weber-Rendu disease, Rendu-Osler-Weber disease,
Xenbase Genes : gdf2, acvrl1, smad4, smad10, eng
|MONDO:0019180 - hereditary hemorrhagic telangiectasia|
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee