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

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-LHRLMTG3-J .

vh8: a skos:ConceptScheme .
vh8:-RFF18FW6-W
  skos:prefLabel "kératodermie"@fr, "keratoderma"@en ;
  a skos:Concept ;
  skos:narrower vh8:-LHRLMTG3-J .

vh8:-LHRLMTG3-J
  skos:prefLabel "kératodermie palmoplantaire de Méléda"@fr, "Meleda disease"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Meleda_disease> ;
  skos:broader vh8:-N32K7HZ8-D, vh8:-RFF18FW6-W ;
  skos:altLabel "mal de Méléda"@fr, "maladie de Méléda"@fr, "kératodermie palmoplantaire transgrédiente"@fr, "keratoderma palmoplantaris transgrediens"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:definition "Meleda disease (MDM) or \"mal de Meleda\", also called Mljet disease, keratosis palmoplantaris and transgradiens of Siemens, (also known as \"acral keratoderma\", \"mutilating palmoplantar keratoderma of the Gamborg-Nielsen type\", \"palmoplantar ectodermal dysplasia type VIII\", and \"palmoplantar keratoderma of the Norrbotten type\") is an extremely rare autosomal recessive congenital skin disorder in which dry, thick patches of skin develop on the soles of the hands and feet, a condition known as palmoplantar hyperkeratosis. (Wikipedia)"@en .