@prefix vh8: <http://data.loterre.fr/ark:/67375/VH8> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-RD0N82HM-J .

vh8: a skos:ConceptScheme .
vh8:-RD0N82HM-J
  skos:definition "Léri–Weill dyschondrosteosis or LWD is a rare pseudoautosomal dominant genetic disorder which results in dwarfism with short forearms and legs (mesomelic dwarfism) and a bayonet-like deformity of the forearms (Madelung's deformity). (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-CZGBG75B-L, vh8:-N32K7HZ8-D ;
  skos:prefLabel "dyschondrostéose"@fr, "dyschondrosteosis"@en ;
  skos:altLabel "maladie de Léri-Weill"@fr ;
  skos:exactMatch <https://en.wikipedia.org/wiki/L%C3%A9ri%E2%80%93Weill_dyschondrosteosis> .

vh8:-CZGBG75B-L
  skos:prefLabel "osteochondrodysplasia"@en, "ostéochondrodysplasie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-RD0N82HM-J .