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Disease Ontology Browser
hereditary hemorrhagic telangiectasia (DOID:1270)
Alliance: disease page
Synonyms: Osler hemorrhagic telangiectasia syndrome; Osler-Weber-Rendu disease; Rendu-Osler-Weber disease
Alt IDs: OMIM:187300, OMIM:600376, OMIM:601101, OMIM:615506, ICD10CM:I78.0, ICD9CM:448.0, MESH:D013683, NCI:C35064, ORDO:774, UMLS_CUI:C0039445
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.

Disease References using Mouse Models (9)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.23
The Jackson Laboratory