Resource: wordnet/30/noun/autosomal_dominant_disease_1_26_00

This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/autosomal_dominant_disease_1_26_00. A machine-readable RDF version of this description is provided here.

rdfs:commenta disease caused by a dominant mutant gene on an autosome ('en' language string)
rdfs:labelautosomal dominant disease ('en' language string)
rdfs:labelautosomal dominant disorder ('en' language string)
lvont:broaderlexvo:wordnet/30/noun/genetic_disease_1_26_00
lvont:labellexvo:term/eng/autosomal%20dominant%20disease
lvont:labellexvo:term/eng/autosomal%20dominant%20disorder
lvont:narrowerlexvo:wordnet/30/noun/Huntington%27s_chorea_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/Marfan%27s_syndrome_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/malignant_hyperthermia_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/neurofibromatosis_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/osteogenesis_imperfecta_1_26_00
lvont:nearlySameAshttp://purl.org/vocabularies/princeton/wn30/synset-autosomal_dominant_disease-noun-1
skos:noteThis 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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