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

vh8:-B3NDDTV7-2
  skos:prefLabel "maxillary disease"@en, "pathologie des maxillaires"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-HLG1B0Z1-X .

vh8:-HLG1B0Z1-X
  skos:broader vh8:-B3NDDTV7-2, vh8:-VWN87BX9-T, vh8:-F0Q8HP18-R, vh8:-KPWN34BB-M, vh8:-HWD5JP3B-D, vh8:-N32K7HZ8-D, vh8:-GWW0QZ9W-Q, vh8:-MBLSJ4C4-D, vh8:-GS4WGJQ9-4 ;
  skos:prefLabel "Hallermann-Streiff-François syndrome"@en, "syndrome d'Hallermann-Streiff-François"@fr ;
  a skos:Concept ;
  skos:definition "Hallermann–Streiff syndrome is a congenital disorder that affects growth, cranial development, hair growth and dental development. (Wikipedia)"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Hallermann%E2%80%93Streiff_syndrome> ;
  skos:inScheme vh8: .

vh8:-MBLSJ4C4-D
  skos:prefLabel "microphtalmie"@fr, "microphthalmia"@en ;
  a skos:Concept ;
  skos:narrower vh8:-HLG1B0Z1-X .

vh8:-HWD5JP3B-D
  skos:prefLabel "nanisme"@fr, "dwarfism"@en ;
  a skos:Concept ;
  skos:narrower vh8:-HLG1B0Z1-X .

vh8:-F0Q8HP18-R
  skos:prefLabel "malformation"@fr, "malformation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-HLG1B0Z1-X .

vh8: a skos:ConceptScheme .
vh8:-GWW0QZ9W-Q
  skos:prefLabel "dysplasie osseuse"@fr, "bone dysplasia"@en ;
  a skos:Concept ;
  skos:narrower vh8:-HLG1B0Z1-X .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-HLG1B0Z1-X .

vh8:-GS4WGJQ9-4
  skos:prefLabel "cataracte"@fr, "cataract"@en ;
  a skos:Concept ;
  skos:narrower vh8:-HLG1B0Z1-X .

vh8:-KPWN34BB-M
  skos:prefLabel "maladie rare"@fr, "rare disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-HLG1B0Z1-X .

vh8:-VWN87BX9-T
  skos:prefLabel "hypotrichose"@fr, "hypotrichosis"@en ;
  a skos:Concept ;
  skos:narrower vh8:-HLG1B0Z1-X .