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

vh8:-ZZLLJ77K-B
  a skos:Concept ;
  skos:broader vh8:-QG1RVCT9-L, vh8:-M7X3NL2G-F, vh8:-JC70JX65-Z ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Elejalde_syndrome> ;
  skos:inScheme vh8: ;
  skos:prefLabel "syndrome d'Elejalde"@fr, "Elejalde syndrome"@en ;
  skos:definition "Elejalde syndrome is an extremely rare autosomal recessive syndrome (only around 10 cases known) consisting of moderate pigment dilution, profound primary neurologic defects, no immune defects, and hair with metallic silvery sheen.It is associated with MYO5A. (Wikipedia)"@en ;
  skos:altLabel "neuroectodermal melanolysosomal disease"@en .

vh8:-JC70JX65-Z
  skos:prefLabel "central nervous system diseases"@en, "pathologie du système nerveux central"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-ZZLLJ77K-B .

vh8: a skos:ConceptScheme .
vh8:-M7X3NL2G-F
  skos:prefLabel "pathologie de la peau"@fr, "skin disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-ZZLLJ77K-B .

vh8:-QG1RVCT9-L
  skos:prefLabel "complex syndrome"@en, "syndrome complexe"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-ZZLLJ77K-B .