This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/galactosemia_1_26_00. A machine-readable RDF version of this description is provided here.
| rdfs:comment | a genetic disease (autosomal recessive) in which an enzyme needed to metabolize galactose is deficient or absent; typically develops shortly after birth ('en' language string) |
| rdfs:label | galactosemia ('en' language string) |
| lvont:broader | lexvo:wordnet/30/noun/inborn_error_of_metabolism_1_26_00 |
| lvont:label | lexvo:term/eng/galactosemia |
| lvont:nearlySameAs | http://purl.org/vocabularies/princeton/wn30/synset-galactosemia-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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