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

vh8:-HQVVF9T2-C
  skos:prefLabel "neuronal ceroid lipofuscinosis"@en, "céroïde lipofuscinose neuronale"@fr ;
  a skos:Concept ;
  skos:broader vh8:-RPL8R9P9-Z .

vh8:-NWHZ184V-G
  skos:prefLabel "leucodystrophie métachromatique"@fr, "metachromatic leukodystrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-RPL8R9P9-Z .

vh8:-PLFNN4S2-4
  skos:prefLabel "metabolic diseases"@en, "maladie métabolique"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-RPL8R9P9-Z .

vh8:-G37XWGTK-R
  skos:prefLabel "enzymopathy"@en, "enzymopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-RPL8R9P9-Z .

vh8:-WTQ25R5S-1
  skos:prefLabel "aspartylglucosaminurie"@fr, "aspartylglucosaminuria"@en ;
  a skos:Concept ;
  skos:broader vh8:-RPL8R9P9-Z .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-RPL8R9P9-Z .

vh8:-RPL8R9P9-Z
  skos:prefLabel "pathologie des lysosomes"@fr, "lysosomal storage disease"@en ;
  skos:inScheme vh8: ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Lysosomal_storage_disease> ;
  skos:narrower vh8:-CLBZF9F6-1, vh8:-F7XJ1KPX-R, vh8:-WTQ25R5S-1, vh8:-HQVVF9T2-C, vh8:-NWHZ184V-G ;
  skos:broader vh8:-G37XWGTK-R, vh8:-N32K7HZ8-D, vh8:-PLFNN4S2-4 ;
  a skos:Concept ;
  skos:definition "Lysosomal storage diseases (LSDs) are a group of about 50 rare inherited metabolic disorders that result from defects in lysosomal function. (Wikipedia)"@en .

vh8:-F7XJ1KPX-R
  skos:prefLabel "sphingolipidosis"@en, "sphingolipidose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-RPL8R9P9-Z .

vh8:-CLBZF9F6-1
  skos:prefLabel "cystinosis"@en, "cystinose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-RPL8R9P9-Z .