This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/Tay-Sachs_disease_1_26_00. A machine-readable RDF version of this description is provided here.
| rdfs:comment | a hereditary disorder of lipid metabolism occurring most frequently in individuals of Jewish descent in eastern Europe; accumulation of lipids in nervous tissue results in death in early childhood ('en' language string) |
| rdfs:label | Sachs disease ('en' language string) |
| rdfs:label | Tay-Sachs disease ('en' language string) |
| rdfs:label | Tay-Sachs ('en' language string) |
| rdfs:label | infantile amaurotic idiocy ('en' language string) |
| lvont:broader | lexvo:wordnet/30/noun/autosomal_recessive_disease_1_26_00 |
| lvont:broader | lexvo:wordnet/30/noun/lipidosis_1_26_00 |
| lvont:broader | lexvo:wordnet/30/noun/monogenic_disorder_1_26_00 |
| lvont:label | lexvo:term/eng/Sachs%20disease |
| lvont:label | lexvo:term/eng/Tay-Sachs%20disease |
| lvont:label | lexvo:term/eng/Tay-Sachs |
| lvont:label | lexvo:term/eng/infantile%20amaurotic%20idiocy |
| lvont:nearlySameAs | http://purl.org/vocabularies/princeton/wn30/synset-Tay-Sachs_disease-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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