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

vh8:-TX6ZBC03-T
  skos:prefLabel "dysmorphie faciale"@fr, "dysmorphic facies"@en ;
  a skos:Concept ;
  skos:narrower vh8:-ZN8MGQFL-6 .

vh8:-K74MDW6H-R
  skos:prefLabel "craniosynostose"@fr, "craniosynostosis"@en ;
  a skos:Concept ;
  skos:narrower vh8:-ZN8MGQFL-6 .

vh8:-ZN8MGQFL-6
  skos:broader vh8:-R185SPCB-Q, vh8:-GLPH3NFD-H, vh8:-N32K7HZ8-D, vh8:-L20NFJQD-3, vh8:-TX6ZBC03-T, vh8:-JW4BV3J7-L, vh8:-K74MDW6H-R, vh8:-QG1RVCT9-L ;
  skos:prefLabel "syndrome de Lin-Gettig"@fr, "Lin-Gettig syndrome"@en ;
  a skos:Concept ;
  skos:inScheme vh8: .

vh8: a skos:ConceptScheme .
vh8:-GLPH3NFD-H
  skos:prefLabel "hypogonadisme"@fr, "hypogonadism"@en ;
  a skos:Concept ;
  skos:narrower vh8:-ZN8MGQFL-6 .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-ZN8MGQFL-6 .

vh8:-R185SPCB-Q
  skos:prefLabel "pathologie de l'appareil circulatoire"@fr, "cardiovascular disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-ZN8MGQFL-6 .

vh8:-QG1RVCT9-L
  skos:prefLabel "complex syndrome"@en, "syndrome complexe"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-ZN8MGQFL-6 .

vh8:-L20NFJQD-3
  skos:prefLabel "corpus callosum agenesis"@en, "agénésie du corps calleux"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-ZN8MGQFL-6 .

vh8:-JW4BV3J7-L
  skos:prefLabel "arriération mentale"@fr, "mental retardation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-ZN8MGQFL-6 .