This Lexvo.org page describes the entity referred to by the URI http://lexvo.org/id/wordnet/30/noun/X-linked_SCID_1_26_00. A machine-readable RDF version of this description is provided here.
| rdfs:comment | SCID in male children resulting from mutation of a gene that codes for a protein on the surface of T cells that allows them to develop a growth factor receptor ('en' language string) |
| rdfs:label | X-SCID ('en' language string) |
| rdfs:label | X-linked SCID ('en' language string) |
| lvont:broader | lexvo:wordnet/30/noun/severe_combined_immunodeficiency_1_26_00 |
| lvont:label | lexvo:term/eng/X-SCID |
| lvont:label | lexvo:term/eng/X-linked%20SCID |
| lvont:nearlySameAs | http://purl.org/vocabularies/princeton/wn30/synset-X-linked_SCID-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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