Resource: wordnet/30/noun/genetic_disease_1_26_00

This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/genetic_disease_1_26_00. A machine-readable RDF version of this description is provided here.

rdfs:commenta disease or disorder that is inherited genetically ('en' language string)
rdfs:labelcongenital disease ('en' language string)
rdfs:labelgenetic abnormality ('en' language string)
rdfs:labelgenetic defect ('en' language string)
rdfs:labelgenetic disease ('en' language string)
rdfs:labelgenetic disorder ('en' language string)
rdfs:labelhereditary condition ('en' language string)
rdfs:labelhereditary disease ('en' language string)
rdfs:labelinherited disease ('en' language string)
rdfs:labelinherited disorder ('en' language string)
lvont:broaderlexvo:wordnet/30/noun/disease_1_26_00
lvont:labellexvo:term/eng/congenital%20disease
lvont:labellexvo:term/eng/genetic%20abnormality
lvont:labellexvo:term/eng/genetic%20defect
lvont:labellexvo:term/eng/genetic%20disease
lvont:labellexvo:term/eng/genetic%20disorder
lvont:labellexvo:term/eng/hereditary%20condition
lvont:labellexvo:term/eng/hereditary%20disease
lvont:labellexvo:term/eng/inherited%20disease
lvont:labellexvo:term/eng/inherited%20disorder
lvont:narrowerlexvo:wordnet/30/noun/Fanconi%27s_anemia_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/Hirschsprung%27s_disease_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/McArdle%27s_disease_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/Spielmeyer-Vogt_disease_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/abetalipoproteinemia_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/achondroplasia_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/autosomal_dominant_disease_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/autosomal_recessive_disease_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/congenital_afibrinogenemia_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/dwarfism_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/hepatolenticular_degeneration_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/hyperbetalipoproteinemia_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/ichthyosis_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/inborn_error_of_metabolism_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/lactose_intolerance_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/maple_syrup_urine_disease_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/monogenic_disorder_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/mucopolysaccharidosis_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/muscular_dystrophy_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/nevoid_elephantiasis_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/oligodactyly_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/oligodontia_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/osteopetrosis_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/otosclerosis_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/polygenic_disorder_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/porphyria_1_26_00
lvont:nearlySameAshttp://purl.org/vocabularies/princeton/wn30/synset-genetic_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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