@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:-XG4MLTB9-J .

vh8:-JNKW3X3N-9
  skos:prefLabel "urticaria"@en, "urticaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-XG4MLTB9-J .

vh8:-WPZTLQNX-2
  skos:prefLabel "inflammatory disease"@en, "maladie inflammatoire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-XG4MLTB9-J .

vh8:-KQ77D01G-M
  skos:prefLabel "amyloidosis"@en, "amyloïdose"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-XG4MLTB9-J .

vh8:-XG4MLTB9-J
  skos:inScheme vh8: ;
  skos:definition "Muckle–Wells syndrome (MWS), is a rare autosomal dominant disease which causes sensorineural deafness and recurrent hives, and can lead to amyloidosis. (Wikipedia)"@en ;
  skos:prefLabel "Muckle-Wells syndrome"@en, "syndrome de Muckle et Wells"@fr ;
  skos:broader vh8:-WPZTLQNX-2, vh8:-KQ77D01G-M, vh8:-N32K7HZ8-D, vh8:-QRLBC1VS-W, vh8:-JNKW3X3N-9 ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Muckle%E2%80%93Wells_syndrome>, <https://www.wikidata.org/wiki/Q1538218> ;
  a skos:Concept ;
  skos:altLabel "amylose héréditaire avec neuropathie, surdité et urticaire"@fr .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-XG4MLTB9-J .