This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/oculopharyngeal_muscular_dystrophy_1_26_00. A machine-readable RDF version of this description is provided here.
| rdfs:comment | a form of muscular dystrophy that usually begins between early adulthood and middle age and first affects muscles of the eyelid and throat; progresses slowly with swallowing problems common as the disease progresses; inheritance is autosomal dominant ('en' language string) |
| rdfs:label | oculopharyngeal muscular dystrophy ('en' language string) |
| lvont:broader | lexvo:wordnet/30/noun/muscular_dystrophy_1_26_00 |
| lvont:label | lexvo:term/eng/oculopharyngeal%20muscular%20dystrophy |
| lvont:nearlySameAs | http://purl.org/vocabularies/princeton/wn30/synset-oculopharyngeal_muscular_dystrophy-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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