This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/von_Willebrand%27s_disease_1_26_00. A machine-readable RDF version of this description is provided here.
| rdfs:comment | a form of hemophilia discovered by Erik von Willebrand; a genetic disorder that is inherited as an autosomal recessive trait; characterized by a deficiency of the coagulation factor and by mucosal bleeding ('en' language string) |
| rdfs:label | angiohemophilia ('en' language string) |
| rdfs:label | vascular hemophilia ('en' language string) |
| rdfs:label | von Willebrand's disease ('en' language string) |
| lvont:broader | lexvo:wordnet/30/noun/hemophilia_1_26_00 |
| lvont:label | lexvo:term/eng/angiohemophilia |
| lvont:label | lexvo:term/eng/vascular%20hemophilia |
| lvont:label | lexvo:term/eng/von%20Willebrand's%20disease |
| lvont:nearlySameAs | http://purl.org/vocabularies/princeton/wn30/synset-von_Willebrand's_disease-noun-1 |
| skos:note | This resource corresponds to the meaning of the gloss text. It shares its meaning with that of the synonym set rather than denoting the WordNet synset. ('en' language string) |
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