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

vh8:-CT80X962-7
  skos:inScheme vh8: ;
  skos:altLabel "tyrosinemia type II"@en, "tyrosinémie oculocutanée"@fr, "syndrome de Richner-Hanhart"@fr, "oculocutaneous tyrosinemia"@en ;
  skos:prefLabel "Richner-Hanhart’s syndrome"@en, "kératodermie palmoplantaire de Richner-Hanhart"@fr ;
  skos:broader vh8:-RFF18FW6-W, vh8:-N38H9W6C-W ;
  a skos:Concept ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Tyrosinemia_type_II> ;
  skos:definition "Tyrosinemia type II is an autosomal recessive condition with onset between ages 2 and 4 years, when painful circumscribed calluses develop on the pressure points of the palm of the hand and sole of the foot. (Wikipedia)"@en .

vh8:-N38H9W6C-W
  skos:prefLabel "tyrosinémie"@fr, "tyrosinemia"@en ;
  a skos:Concept ;
  skos:narrower vh8:-CT80X962-7 .

vh8: a skos:ConceptScheme .
vh8:-RFF18FW6-W
  skos:prefLabel "kératodermie"@fr, "keratoderma"@en ;
  a skos:Concept ;
  skos:narrower vh8:-CT80X962-7 .