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

vh8:-K32X84J6-5
  skos:prefLabel "dysgénésie"@fr, "dysgenesis"@en ;
  a skos:Concept ;
  skos:narrower vh8:-B05R8XD0-M .

vh8: a skos:ConceptScheme .
vh8:-CCS31G12-M
  skos:prefLabel "endocrinopathy"@en, "endocrinopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-B05R8XD0-M .

vh8:-KBVM42F0-G
  skos:prefLabel "aberration chromosomique"@fr, "chromosomal aberration"@en ;
  a skos:Concept ;
  skos:narrower vh8:-B05R8XD0-M .

vh8:-HZH1232K-0
  skos:prefLabel "sexual differentiation disorder"@en, "anomalie de la différenciation sexuelle"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-B05R8XD0-M .

vh8:-B05R8XD0-M
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-KBVM42F0-G, vh8:-K32X84J6-5, vh8:-HZH1232K-0, vh8:-CCS31G12-M ;
  skos:prefLabel "syndrome 46XX mâle"@fr, "46XX male syndrome"@en .