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

vh8:-HSN6FQV2-2
  skos:prefLabel "syndrome de Smith-Magenis"@fr, "Smith-Magenis syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-VHC1KLXN-D .

vh8:-JDMT1W7S-5
  skos:prefLabel "diencephalic syndrome"@en, "syndrome diencéphalique"@fr ;
  a skos:Concept ;
  skos:broader vh8:-VHC1KLXN-D .

vh8:-VHC1KLXN-D
  skos:prefLabel "retard staturopondéral"@fr, "growth retardation"@en ;
  skos:narrower vh8:-KR80TQCJ-9, vh8:-P9Q0F9M2-F, vh8:-HSN6FQV2-2, vh8:-SMS1K39H-4, vh8:-W0G5H2BS-L, vh8:-RZR694NR-W, vh8:-JDMT1W7S-5 ;
  skos:broader vh8:-C9MBQL41-N ;
  a skos:Concept ;
  skos:altLabel "retard statural"@fr ;
  skos:definition "Un retard de croissance staturo-pondérale est un terme médical désignant une croissance insuffisante sur le plan de la taille et/ou du poids, durant la phase de développement de l'enfant. (Wikipédia)"@fr, "Failure to thrive (FTT) indicates insufficient weight gain or inappropriate weight loss in pediatric patients unless the term is more precisely defined. (Wikipedia)"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Failure_to_thrive>, <https://fr.wikipedia.org/wiki/Retard_de_croissance_staturo-pond%C3%A9rale> ;
  skos:inScheme vh8: .

vh8:-KR80TQCJ-9
  skos:prefLabel "Dubowitz syndrome"@en, "syndrome de Dubowitz"@fr ;
  a skos:Concept ;
  skos:broader vh8:-VHC1KLXN-D .

vh8: a skos:ConceptScheme .
vh8:-SMS1K39H-4
  skos:prefLabel "Marinesco-Sjögren syndrome"@en, "syndrome de Marinesco-Sjögren"@fr ;
  a skos:Concept ;
  skos:broader vh8:-VHC1KLXN-D .

vh8:-W0G5H2BS-L
  skos:prefLabel "Mauriac syndrome"@en, "syndrome de Mauriac"@fr ;
  a skos:Concept ;
  skos:broader vh8:-VHC1KLXN-D .

vh8:-P9Q0F9M2-F
  skos:prefLabel "syndrome de Pitt-Rogers-Danks"@fr, "Pitt-Rogers-Danks syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-VHC1KLXN-D .

vh8:-C9MBQL41-N
  skos:prefLabel "developmental disorder"@en, "trouble du développement"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-VHC1KLXN-D .

vh8:-RZR694NR-W
  skos:prefLabel "syndrome de Watson"@fr, "Watson syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-VHC1KLXN-D .