This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/neurofibromatosis_1_26_00. A machine-readable RDF version of this description is provided here.
| rdfs:comment | autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities ('en' language string) |
| rdfs:label | neurofibromatosis ('en' language string) |
| rdfs:label | von Recklinghausen's disease ('en' language string) |
| lvont:broader | lexvo:wordnet/30/noun/autosomal_dominant_disease_1_26_00 |
| lvont:broader | lexvo:wordnet/30/noun/monogenic_disorder_1_26_00 |
| lvont:label | lexvo:term/eng/neurofibromatosis |
| lvont:label | lexvo:term/eng/von%20Recklinghausen's%20disease |
| lvont:nearlySameAs | http://purl.org/vocabularies/princeton/wn30/synset-neurofibromatosis-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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