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

vh8:-BSFBPL4W-S
  skos:prefLabel "diseases of the osteoarticular system"@en, "pathologie du système ostéoarticulaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-JL5T2HJT-9 .

vh8:-C0CS7VBM-F
  skos:prefLabel "pathologie de l'oeil"@fr, "eye disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-JL5T2HJT-9 .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-JL5T2HJT-9 .

vh8:-QG1RVCT9-L
  skos:prefLabel "complex syndrome"@en, "syndrome complexe"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-JL5T2HJT-9 .

vh8:-JL5T2HJT-9
  skos:inScheme vh8: ;
  skos:prefLabel "syndrome de Weill-Marchesani"@fr, "Weill-Marchesani syndrome"@en ;
  skos:broader vh8:-BSFBPL4W-S, vh8:-N32K7HZ8-D, vh8:-QG1RVCT9-L, vh8:-C0CS7VBM-F ;
  skos:definition "Weill–Marchesani syndrome is a rare genetic disorder characterized by short stature; an unusually short, broad head (brachycephaly) and other facial abnormalities; hand defects, including unusually short fingers (brachydactyly); and distinctive eye (ocular) abnormalities. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Weill%E2%80%93Marchesani_syndrome>, <https://www.wikidata.org/wiki/Q3961695> .