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

vh8:-LZM6115J-1
  skos:prefLabel "chromosome X surnuméraire"@fr, "supernumerary X chromosome"@en ;
  a skos:Concept ;
  skos:narrower vh8:-K0LQ98NK-L .

vh8:-F0Q8HP18-R
  skos:prefLabel "malformation"@fr, "malformation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-K0LQ98NK-L .

vh8: a skos:ConceptScheme .
vh8:-K0LQ98NK-L
  skos:prefLabel "syndrome de Klinefelter"@fr, "Klinefelter syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-BBD37W0Z-W, vh8:-ZPH8ZCRP-X, vh8:-H4HTCN3V-2, vh8:-LZM6115J-1, vh8:-F0Q8HP18-R, vh8:-HZH1232K-0 ;
  skos:definition "Le syndrome de Klinefelter ou 47,XXY est une aneuploïdie qui se caractérise chez l'humain par un chromosome sexuel X supplémentaire. (Wikipédia)"@fr, "Klinefelter syndrome (KS), also known as 47,XXY or XXY, is the set of symptoms that result from two or more X chromosomes in males. (Wikipedia)"@en ;
  skos:inScheme vh8: ;
  skos:exactMatch <https://fr.wikipedia.org/wiki/Syndrome_de_Klinefelter>, <https://en.wikipedia.org/wiki/Klinefelter_syndrome> .

vh8:-H4HTCN3V-2
  skos:prefLabel "stérilité mâle"@fr, "male sterility"@en ;
  a skos:Concept ;
  skos:narrower vh8:-K0LQ98NK-L .

vh8:-ZPH8ZCRP-X
  skos:prefLabel "retard pubertaire"@fr, "delayed puberty"@en ;
  a skos:Concept ;
  skos:narrower vh8:-K0LQ98NK-L .

vh8:-BBD37W0Z-W
  skos:prefLabel "hypogonadisme hypergonadotrope"@fr, "hypergonadotropic hypogonadism"@en ;
  a skos:Concept ;
  skos:narrower vh8:-K0LQ98NK-L .

vh8:-HZH1232K-0
  skos:prefLabel "sexual differentiation disorder"@en, "anomalie de la différenciation sexuelle"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-K0LQ98NK-L .