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

vh8:-KJH4TT33-B
  skos:prefLabel "lipomucopolysaccharidose"@fr, "lipomucopolysaccharidosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-M8W0T5JK-9 .

vh8:-M8W0T5JK-9
  skos:narrower vh8:-KJH4TT33-B, vh8:-HCL3BNVF-M, vh8:-DXX5T8JG-Z, vh8:-R6HSWL6Z-3, vh8:-VMQZD51M-H ;
  skos:inScheme vh8: ;
  skos:broader vh8:-N32K7HZ8-D, vh8:-PLFNN4S2-4, vh8:-G37XWGTK-R ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Mucolipidosis> ;
  skos:definition "Mucolipidosis is a group of inherited metabolic disorders that affect the body's ability to carry out the normal turnover of various materials within cells.When originally named, the mucolipidoses derived their name from the similarity in presentation to both mucopolysaccharidoses and sphingolipidoses. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:prefLabel "mucolipidosis"@en, "mucolipidose"@fr .

vh8:-VMQZD51M-H
  skos:prefLabel "mucolipidosis IV"@en, "mucolipidose IV"@fr ;
  a skos:Concept ;
  skos:broader vh8:-M8W0T5JK-9 .

vh8:-HCL3BNVF-M
  skos:prefLabel "I-cell disease"@en, "mucolipidose II"@fr ;
  a skos:Concept ;
  skos:broader vh8:-M8W0T5JK-9 .

vh8:-PLFNN4S2-4
  skos:prefLabel "metabolic diseases"@en, "maladie métabolique"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-M8W0T5JK-9 .

vh8:-G37XWGTK-R
  skos:prefLabel "enzymopathy"@en, "enzymopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-M8W0T5JK-9 .

vh8:-DXX5T8JG-Z
  skos:prefLabel "mucolipidose III"@fr, "mucolipidosis III"@en ;
  a skos:Concept ;
  skos:broader vh8:-M8W0T5JK-9 .

vh8:-R6HSWL6Z-3
  skos:prefLabel "mannosidose"@fr, "mannosidosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-M8W0T5JK-9 .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-M8W0T5JK-9 .