Resource: wordnet/30/noun/severe_combined_immunodeficiency_1_26_00

This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/severe_combined_immunodeficiency_1_26_00. A machine-readable RDF version of this description is provided here.

rdfs:commenta congenital disease affecting T cells that can result from a mutation in any one of several different genes; children with it are susceptible to infectious disease; if untreated it is lethal within the first year or two of life ('en' language string)
rdfs:labelSCID ('en' language string)
rdfs:labelsevere combined immunodeficiency disease ('en' language string)
rdfs:labelsevere combined immunodeficiency ('en' language string)
lvont:broaderlexvo:wordnet/30/noun/immunodeficiency_1_26_00
lvont:broaderlexvo:wordnet/30/noun/monogenic_disorder_1_26_00
lvont:labellexvo:term/eng/SCID
lvont:labellexvo:term/eng/severe%20combined%20immunodeficiency%20disease
lvont:labellexvo:term/eng/severe%20combined%20immunodeficiency
lvont:narrowerlexvo:wordnet/30/noun/ADA-SCID_1_26_00
lvont:narrowerlexvo:wordnet/30/noun/X-linked_SCID_1_26_00
lvont:nearlySameAshttp://purl.org/vocabularies/princeton/wn30/synset-severe_combined_immunodeficiency-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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