autosomal dominant disease hereditary hemorrhagic telangiectasia GARD:6626 ICD10CM:I78.0 Xref MGI. OMIM mapping confirmed by DO. [SN]. disease_ontology A vascular disease characterized by the presence of multiple arteriovenous malformations that lack intervening capillaries and result in direct connections between arteries and veins. OMIM:615506 OMIM:601101 OMIM:600376 MESH:D013683 OMIM:187300 ICD9CM:448.0 DOID:1270 Osler-Weber-Rendu disease Rendu-Osler-Weber disease UMLS_CUI:C0039445 ORDO:774 NCI:C35064 Osler hemorrhagic telangiectasia syndrome SNOMEDCT_US_2020_03_01:266324004 vascular disease