This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/abetalipoproteinemia_1_26_00. A machine-readable RDF version of this description is provided here.
| rdfs:comment | a rare inherited disorder of fat metabolism; characterized by severe deficiency of beta-lipoproteins and abnormal red blood cells (acanthocytes) and abnormally low cholesterol levels ('en' language string) |
| rdfs:label | abetalipoproteinemia ('en' language string) |
| lvont:broader | lexvo:wordnet/30/noun/genetic_disease_1_26_00 |
| lvont:broader | lexvo:wordnet/30/noun/hypobetalipoproteinemia_1_26_00 |
| lvont:broader | lexvo:wordnet/30/noun/lipidosis_1_26_00 |
| lvont:label | lexvo:term/eng/abetalipoproteinemia |
| lvont:nearlySameAs | http://purl.org/vocabularies/princeton/wn30/synset-abetalipoproteinemia-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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