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

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-TKPTT4NP-M .

vh8:-TKPTT4NP-M
  skos:definition "Triple-A syndrome or AAA syndrome, is a rare autosomal recessive congenital disorder. In most cases, there is no family history of it. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-R4DS6SK9-L, vh8:-QXQ7P3NM-K, vh8:-N32K7HZ8-D ;
  skos:prefLabel "syndrome d'Allgrove"@fr, "Allgrove syndrome"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Triple-A_syndrome> .

vh8:-QXQ7P3NM-K
  skos:prefLabel "adrenal insufficiency"@en, "insuffisance surrénalienne"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-TKPTT4NP-M .

vh8:-R4DS6SK9-L
  skos:prefLabel "pathologie de l'oesophage"@fr, "esophageal disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-TKPTT4NP-M .

