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

vh8:-W790N3DT-N
  skos:prefLabel "aminoacid disorder"@en, "aminoacidopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-MXJQPW9J-9 .

vh8:-XZJTZ9TJ-J
  skos:prefLabel "biological abnormality"@en, "anomalie biologique"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-MXJQPW9J-9 .

vh8:-DPVF24QV-B
  skos:prefLabel "trouble métabolique"@fr, "metabolic disorder"@en ;
  a skos:Concept ;
  skos:narrower vh8:-MXJQPW9J-9 .

vh8: a skos:ConceptScheme .
vh8:-MXJQPW9J-9
  skos:definition "Ornithine translocase deficiency, also called hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome, is a rare autosomal recessive urea cycle disorder affecting the enzyme ornithine translocase, which causes ammonia to accumulate in the blood, a condition called hyperammonemia. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-DPVF24QV-B, vh8:-W790N3DT-N, vh8:-XZJTZ9TJ-J ;
  skos:prefLabel "hyperornithinémie"@fr, "hyperornithinemia"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Ornithine_translocase_deficiency> .