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Disease Ontology Browser
hereditary hemorrhagic telangiectasia (DOID:1270)
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: An autosomal dominant 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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/18/2017
MGI 6.08
The Jackson Laboratory