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

vh8:-QWCXFWK5-7
  skos:prefLabel "gynécomastie"@fr, "gynecomasty"@en ;
  a skos:Concept ;
  skos:narrower vh8:-KXN51K6K-L .

vh8:-R46M4MN1-K
  skos:prefLabel "hypospadias"@fr, "hypospadias"@en ;
  a skos:Concept ;
  skos:narrower vh8:-KXN51K6K-L .

vh8:-KXN51K6K-L
  skos:inScheme vh8: ;
  skos:broader vh8:-VP0ZRTDF-7, vh8:-QWCXFWK5-7, vh8:-R46M4MN1-K, vh8:-GLPH3NFD-H, vh8:-N32K7HZ8-D ;
  a skos:Concept ;
  skos:definition "Partial androgen insensitivity syndrome (PAIS) is a condition that results in the partial inability of the cell to respond to androgens. (Wikipedia)"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Partial_androgen_insensitivity_syndrome> ;
  skos:prefLabel "Reifenstein syndrome"@en, "syndrome de Reifenstein"@fr .

vh8:-VP0ZRTDF-7
  skos:prefLabel "cryptorchidism"@en, "cryptorchidie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-KXN51K6K-L .

vh8: a skos:ConceptScheme .
vh8:-GLPH3NFD-H
  skos:prefLabel "hypogonadisme"@fr, "hypogonadism"@en ;
  a skos:Concept ;
  skos:narrower vh8:-KXN51K6K-L .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-KXN51K6K-L .