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

vh8:-QRLBC1VS-W
  skos:prefLabel "surdité de perception"@fr, "perception hearing loss"@en ;
  a skos:Concept ;
  skos:narrower vh8:-P386QDNJ-H .

vh8:-ZV61M3J7-S
  skos:prefLabel "atrophie du nerf optique"@fr, "optic nerve atrophy"@en ;
  a skos:Concept ;
  skos:narrower vh8:-P386QDNJ-H .

vh8:-P386QDNJ-H
  skos:inScheme vh8: ;
  skos:prefLabel "Wolfram syndrome"@en, "syndrome de Wolfram"@fr ;
  skos:broader vh8:-KLPN7GP3-6, vh8:-ZV61M3J7-S, vh8:-QG1RVCT9-L, vh8:-SHG7GR1P-W, vh8:-N32K7HZ8-D, vh8:-QRLBC1VS-W, vh8:-SBQD2SBR-V ;
  skos:exactMatch <https://www.wikidata.org/wiki/Q1153641>, <https://fr.wikipedia.org/wiki/Syndrome_de_Wolfram>, <https://en.wikipedia.org/wiki/Wolfram_syndrome> ;
  a skos:Concept ;
  skos:definition "Le syndrome de Wolfram, également connu sous son acronyme anglophone DIDMOAD (pour « diabetes insipidus, diabetes mellitus, optic atrophy, and deafness ») est un syndrome rare, appartenant au groupe des maladies dites orphelines, qui associe un diabète de type 1, un diabète insipide, un trouble grave de la vision (atrophie optique) et des troubles neurologiques. (Wikipédia)"@fr, "Wolfram syndrome, also called DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness), is a rare autosomal-recessive genetic disorder that causes childhood-onset diabetes mellitus, optic atrophy, and deafness as well as various other possible disorders.It was first described in four siblings in 1938 by Dr. (Wikipedia)"@en .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-P386QDNJ-H .

vh8:-SBQD2SBR-V
  skos:prefLabel "diabète de type 1"@fr, "diabetes mellitus type 1"@en ;
  a skos:Concept ;
  skos:narrower vh8:-P386QDNJ-H .

vh8:-SHG7GR1P-W
  skos:prefLabel "maladie dégénérative"@fr, "degenerative disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-P386QDNJ-H .

vh8:-QG1RVCT9-L
  skos:prefLabel "complex syndrome"@en, "syndrome complexe"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-P386QDNJ-H .

vh8:-KLPN7GP3-6
  skos:prefLabel "diabète insipide"@fr, "diabetes insipidus"@en ;
  a skos:Concept ;
  skos:narrower vh8:-P386QDNJ-H .