This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/myotonic_muscular_dystrophy_1_26_00. A machine-readable RDF version of this description is provided here.
rdfs:comment | a severe form of muscular dystrophy marked by generalized weakness and muscular wasting that affects the face and feet and hands and neck; difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips; the onset can be any time from birth to middle age and the progression is slow; inheritance is autosomal dominant ('en' language string) |
rdfs:label | Steinert's disease ('en' language string) |
rdfs:label | myotonia atrophica ('en' language string) |
rdfs:label | myotonic dystrophy ('en' language string) |
rdfs:label | myotonic muscular dystrophy ('en' language string) |
lvont:broader | lexvo:wordnet/30/noun/muscular_dystrophy_1_26_00 |
lvont:label | lexvo:term/eng/Steinert's%20disease |
lvont:label | lexvo:term/eng/myotonia%20atrophica |
lvont:label | lexvo:term/eng/myotonic%20dystrophy |
lvont:label | lexvo:term/eng/myotonic%20muscular%20dystrophy |
lvont:nearlySameAs | http://purl.org/vocabularies/princeton/wn30/synset-myotonic_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) |
Lexvo.org 2008-2025 Gerard de Melo. Contact Data Sources Legal Information / Imprint