Resource: wordnet/30/noun/myotonic_muscular_dystrophy_1_26_00

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:commenta 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:labelSteinert's disease ('en' language string)
rdfs:labelmyotonia atrophica ('en' language string)
rdfs:labelmyotonic dystrophy ('en' language string)
rdfs:labelmyotonic muscular dystrophy ('en' language string)
lvont:broaderlexvo:wordnet/30/noun/muscular_dystrophy_1_26_00
lvont:labellexvo:term/eng/Steinert's%20disease
lvont:labellexvo:term/eng/myotonia%20atrophica
lvont:labellexvo:term/eng/myotonic%20dystrophy
lvont:labellexvo:term/eng/myotonic%20muscular%20dystrophy
lvont:nearlySameAshttp://purl.org/vocabularies/princeton/wn30/synset-myotonic_muscular_dystrophy-noun-1
skos:noteThis 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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