This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/Charcot-Marie-Tooth_disease_1_26_00. A machine-readable RDF version of this description is provided here.
rdfs:comment | a form of neuropathy that can begin between childhood and young adulthood; characterized by weakness and atrophy of the muscles of the hands and lower legs; progression is slow and individuals affected can have a normal life span; inheritance is X-linked recessive or X-linked dominant ('en' language string) |
rdfs:label | Charcot-Marie-Tooth disease ('en' language string) |
rdfs:label | hereditary motor and sensory neuropathy ('en' language string) |
lvont:broader | lexvo:wordnet/30/noun/neuropathy_1_26_00 |
lvont:label | lexvo:term/eng/Charcot-Marie-Tooth%20disease |
lvont:label | lexvo:term/eng/hereditary%20motor%20and%20sensory%20neuropathy |
lvont:nearlySameAs | http://purl.org/vocabularies/princeton/wn30/synset-Charcot-Marie-Tooth_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) |
Lexvo.org 2008-2025 Gerard de Melo. Contact Data Sources Legal Information / Imprint