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

vh8:-K52TXF4H-M
  skos:broader vh8:-H707N75F-8, vh8:-N32K7HZ8-D, vh8:-TX6ZBC03-T ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Hanhart_syndrome>, <https://www.wikidata.org/wiki/Q9390457> ;
  skos:inScheme vh8: ;
  skos:prefLabel "syndrome de Hanhart"@fr, "Hanhart syndrome"@en ;
  a skos:Concept ;
  skos:definition "Hanhart syndrome (also known as Aglossia adactylia; Hypoglossia-hypodactylia syndrome; Peromelia with micrognathia) is a congenital disorder that causes an undeveloped tongue and malformed extremities and fingers. (Wikipedia)"@en .

vh8:-TX6ZBC03-T
  skos:prefLabel "dysmorphie faciale"@fr, "dysmorphic facies"@en ;
  a skos:Concept ;
  skos:narrower vh8:-K52TXF4H-M .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-K52TXF4H-M .

vh8:-H707N75F-8
  skos:prefLabel "dysostose"@fr, "dysostosis"@en ;
  a skos:Concept ;
  skos:narrower vh8:-K52TXF4H-M .