@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:-KN1MVJP1-7 .

vh8:-DK5V29PH-J
  skos:prefLabel "sténose pulmonaire"@fr, "pulmonary stenosis"@en ;
  a skos:Concept ;
  skos:narrower vh8:-KN1MVJP1-7 .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-KN1MVJP1-7 .

vh8:-QG1RVCT9-L
  skos:prefLabel "complex syndrome"@en, "syndrome complexe"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-KN1MVJP1-7 .

vh8:-KPWN34BB-M
  skos:prefLabel "maladie rare"@fr, "rare disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-KN1MVJP1-7 .

vh8:-KN1MVJP1-7
  skos:definition "Keutel syndrome (KS) is a rare autosomal recessive genetic disorder characterized by abnormal diffuse cartilage calcification, hypoplasia of the mid-face, peripheral pulmonary stenosis, hearing loss, short distal phalanges (tips) of the fingers and mild mental retardation. (Wikipedia)"@en ;
  skos:exactMatch <https://www.wikidata.org/wiki/Q6395632>, <https://en.wikipedia.org/wiki/Keutel_syndrome> ;
  skos:broader vh8:-N32K7HZ8-D, vh8:-NSFJF3XC-X, vh8:-TX6ZBC03-T, vh8:-KPWN34BB-M, vh8:-QG1RVCT9-L, vh8:-DK5V29PH-J ;
  skos:inScheme vh8: ;
  skos:prefLabel "Keutel syndrome"@en, "syndrome de Keutel"@fr ;
  a skos:Concept .

vh8:-NSFJF3XC-X
  skos:prefLabel "brachyphalangie"@fr, "brachyphalangy"@en ;
  a skos:Concept ;
  skos:narrower vh8:-KN1MVJP1-7 .