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

vh8:-N9GBZ8KH-D
  skos:prefLabel "leukodystrophy"@en, "leucodystrophie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-DXNBBM07-X .

vh8: a skos:ConceptScheme .
vh8:-DXNBBM07-X
  skos:broader vh8:-QXQ7P3NM-K, vh8:-F7XJ1KPX-R, vh8:-N9GBZ8KH-D, vh8:-ZG9NH0MB-2 ;
  skos:exactMatch <https://fr.wikipedia.org/wiki/Adr%C3%A9noleucodystrophie_li%C3%A9e_%C3%A0_l%27X>, <https://en.wikipedia.org/wiki/Adrenoleukodystrophy> ;
  skos:prefLabel "adrenoleukodystrophy"@en, "adrénoleucodystrophie"@fr ;
  skos:inScheme vh8: ;
  a skos:Concept ;
  skos:definition "Adrenoleukodystrophy (ALD) is a disease linked to the X chromosome. It is a result of fatty acid buildup caused by the relevant enzymes not functioning properly, which then causes damage to the myelin sheath of the nerves, resulting in seizures and hyperactivity. (Wikipedia)"@en, "L'adrénoleucodystrophie liée à l'X (ALD) est une maladie qui se manifeste par une démyélinisation progressive du système nerveux central ou une insuffisance surrénale périphérique. (Wikipédia)"@fr .

vh8:-QXQ7P3NM-K
  skos:prefLabel "adrenal insufficiency"@en, "insuffisance surrénalienne"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-DXNBBM07-X .

vh8:-ZG9NH0MB-2
  skos:prefLabel "pathologie des peroxysomes"@fr, "peroxisomal disorders"@en ;
  a skos:Concept ;
  skos:narrower vh8:-DXNBBM07-X .

vh8:-F7XJ1KPX-R
  skos:prefLabel "sphingolipidosis"@en, "sphingolipidose"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-DXNBBM07-X .