This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/Hurler%27s_syndrome_1_26_00. A machine-readable RDF version of this description is provided here.
| rdfs:comment | hereditary disease (autosomal recessive) consisting of an error is mucopolysaccharide metabolism; characterized by severe abnormalities in development of skeletal cartilage and bone and mental retardation ('en' language string) |
| rdfs:label | Hurler's disease ('en' language string) |
| rdfs:label | Hurler's syndrome ('en' language string) |
| rdfs:label | dysostosis multiplex ('en' language string) |
| rdfs:label | gargoylism ('en' language string) |
| rdfs:label | lipochondrodystrophy ('en' language string) |
| lvont:broader | lexvo:wordnet/30/noun/monogenic_disorder_1_26_00 |
| lvont:broader | lexvo:wordnet/30/noun/mucopolysaccharidosis_1_26_00 |
| lvont:label | lexvo:term/eng/Hurler's%20disease |
| lvont:label | lexvo:term/eng/Hurler's%20syndrome |
| lvont:label | lexvo:term/eng/dysostosis%20multiplex |
| lvont:label | lexvo:term/eng/gargoylism |
| lvont:label | lexvo:term/eng/lipochondrodystrophy |
| lvont:nearlySameAs | http://purl.org/vocabularies/princeton/wn30/synset-Hurler's_syndrome-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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