@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:-Q6G3GCHC-W .

vh8: a skos:ConceptScheme .
vh8:-M7X3NL2G-F
  skos:prefLabel "pathologie de la peau"@fr, "skin disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-Q6G3GCHC-W .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-Q6G3GCHC-W .

vh8:-Q6G3GCHC-W
  a skos:Concept ;
  skos:broader vh8:-TX6ZBC03-T, vh8:-M7X3NL2G-F, vh8:-N32K7HZ8-D, vh8:-TPWMF78N-7 ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Restrictive_dermopathy>, <https://www.wikidata.org/wiki/Q7316329> ;
  skos:prefLabel "restrictive dermopathy"@en, "dermopathie restrictive"@fr ;
  skos:definition "Restrictive dermopathy is a rare, lethal autosomal recessive skin condition characterized by syndromic facies, tight skin, sparse or absent eyelashes, and secondary joint changes. (Wikipedia)"@en ;
  skos:inScheme vh8: .

vh8:-TPWMF78N-7
  skos:prefLabel "arthrogryposis"@en, "arthrogrypose"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-Q6G3GCHC-W .