This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/phenylketonuria_1_26_00. A machine-readable RDF version of this description is provided here.
| rdfs:comment | a genetic disorder of metabolism; lack of the enzyme needed to turn phenylalanine into tyrosine results in an accumulation of phenylalanine in the body fluids which causes various degrees of mental deficiency ('en' language string) |
| rdfs:label | PKU ('en' language string) |
| rdfs:label | phenylketonuria ('en' language string) |
| lvont:broader | lexvo:wordnet/30/noun/inborn_error_of_metabolism_1_26_00 |
| lvont:label | lexvo:term/eng/PKU |
| lvont:label | lexvo:term/eng/phenylketonuria |
| lvont:nearlySameAs | http://purl.org/vocabularies/princeton/wn30/synset-phenylketonuria-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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