This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/inborn_error_of_metabolism_1_26_00. A machine-readable RDF version of this description is provided here.
rdfs:comment | any of a number of diseases in which an inherited defect (usually a missing or inadequate enzyme) results in an abnormality of metabolism ('en' language string) |
rdfs:label | inborn error of metabolism ('en' language string) |
lvont:broader | lexvo:wordnet/30/noun/genetic_disease_1_26_00 |
lvont:broader | lexvo:wordnet/30/noun/metabolic_disorder_1_26_00 |
lvont:label | lexvo:term/eng/inborn%20error%20of%20metabolism |
lvont:narrower | lexvo:wordnet/30/noun/Niemann-Pick_disease_1_26_00 |
lvont:narrower | lexvo:wordnet/30/noun/galactosemia_1_26_00 |
lvont:narrower | lexvo:wordnet/30/noun/lysinemia_1_26_00 |
lvont:narrower | lexvo:wordnet/30/noun/phenylketonuria_1_26_00 |
lvont:nearlySameAs | http://purl.org/vocabularies/princeton/wn30/synset-inborn_error_of_metabolism-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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