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

vh8:-KXQKDN4H-T
  skos:prefLabel "keratitis"@en, "kératite"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-HMRW6MZQ-3 .

vh8:-C2PD3NRH-2
  skos:prefLabel "hearing loss"@en, "surdité"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-HMRW6MZQ-3 .

vh8: a skos:ConceptScheme .
vh8:-C1LN2JHF-D
  skos:prefLabel "ichtyose"@fr, "ichthyosis"@en ;
  a skos:Concept ;
  skos:narrower vh8:-HMRW6MZQ-3 .

vh8:-QG1RVCT9-L
  skos:prefLabel "complex syndrome"@en, "syndrome complexe"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-HMRW6MZQ-3 .

vh8:-HMRW6MZQ-3
  skos:broader vh8:-QG1RVCT9-L, vh8:-C2PD3NRH-2, vh8:-KXQKDN4H-T, vh8:-C1LN2JHF-D ;
  skos:definition "Keratitis–ichthyosis–deafness syndrome (also known as \"Ichthyosiform erythroderma, corneal involvement, and deafness,\" and \"KID syndrome,\") presents at birth/infancy and is characterized by progressive corneal opacification, either mild generalized hyperkeratosis or discrete erythematous plaques, and neurosensory deafness.It is caused by a mutation in connexin 26. (Wikipedia)"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Keratitis%E2%80%93ichthyosis%E2%80%93deafness_syndrome> ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:prefLabel "syndrome KID"@fr, "KID syndrome"@en ;
  skos:altLabel "keratitis ichthyosis deafness syndrome"@en .