About: hereditary hemorrhagic telangiectasia

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An Entity of Type : owl:Class, within Data Space : demo.openlinksw.com associated with source document(s)

Xref MGI. OMIM mapping confirmed by DO. [SN].

Attributes	Values
type	Class
subClassOf	autosomal dominant disease vascular disease nodeID://b50948540
label	hereditary hemorrhagic telangiectasia
comment	Xref MGI. OMIM mapping confirmed by DO. [SN].
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:1270
database_cross_reference	GARD:6626 ICD10CM:I78.0 ICD9CM:448.0 MESH:D013683 NCI:C35064 OMIM:187300 OMIM:600376 OMIM:601101 OMIM:615506 ORDO:774 SNOMEDCT_US_2021_09_01:266324004 UMLS_CUI:C0039445
has_exact_synonym	Osler hemorrhagic telangiectasia syndrome (en) Osler-Weber-Rendu disease (en) Rendu-Osler-Weber disease (en)
has_obo_namespace	disease_ontology
in_subset	DO_rare_slim NCIthesaurus
http://purl.obolib...g/obo/IAO_0000115	A vascular disease characterized by the presence of multiple arteriovenous malformations that lack intervening capillaries and result in direct connections between arteries and veins.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50948541

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