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

vh8:-F0Q8HP18-R
  skos:prefLabel "malformation"@fr, "malformation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-F9VTM7K5-T .

vh8: a skos:ConceptScheme .
vh8:-GWW0QZ9W-Q
  skos:prefLabel "dysplasie osseuse"@fr, "bone dysplasia"@en ;
  a skos:Concept ;
  skos:narrower vh8:-F9VTM7K5-T .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-F9VTM7K5-T .

vh8:-CZGBG75B-L
  skos:prefLabel "osteochondrodysplasia"@en, "ostéochondrodysplasie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-F9VTM7K5-T .

vh8:-F9VTM7K5-T
  skos:prefLabel "progressive diaphyseal dysplasia"@en, "dysplasie diaphysaire progressive"@fr ;
  skos:broader vh8:-N32K7HZ8-D, vh8:-F0Q8HP18-R, vh8:-GWW0QZ9W-Q, vh8:-CZGBG75B-L ;
  a skos:Concept ;
  skos:definition "Camurati–Engelmann disease (CED) is a very rare autosomal dominant genetic disorder that causes characteristic anomalies in the skeleton.It is also known as progressive diaphyseal dysplasia. (Wikipedia)"@en, "Le syndrome de Camurati-Engelmann est une formation excessive d'os impliquant le crâne et les os longs s'accompagnant de douleurs importantes et de faiblesse musculaire. (Wikipédia)"@fr ;
  skos:exactMatch <https://fr.wikipedia.org/wiki/Syndrome_de_Camurati-Engelmann>, <https://en.wikipedia.org/wiki/Camurati%E2%80%93Engelmann_disease> ;
  skos:inScheme vh8: .