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

vh8:-F0Q8HP18-R
  skos:prefLabel "malformation"@fr, "malformation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-XVNKP097-D .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-XVNKP097-D .

vh8:-QG1RVCT9-L
  skos:prefLabel "complex syndrome"@en, "syndrome complexe"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-XVNKP097-D .

vh8:-XVNKP097-D
  skos:inScheme vh8: ;
  skos:broader vh8:-JW4BV3J7-L, vh8:-F0Q8HP18-R, vh8:-N32K7HZ8-D, vh8:-G2ZSD47D-B, vh8:-QG1RVCT9-L ;
  skos:definition "Hennekam syndrome also known as intestinal lymphagiectasia–lymphedema–mental retardation syndrome, is an autosomal recessive disorder consisting of intestinal lymphangiectasia, facial anomalies, peripheral lymphedema, and mild to moderate levels of growth and intellectual disability.It is also known as \"lymphedema-lymphangiectasia-mental retardation syndrome\".Hennekam Syndrome is subdivided according to the causative genetic lesion, most (or all) of which are affecting the VEGF-C/VEGFR-3 signaling pathway: (Wikipedia)"@en ;
  skos:prefLabel "Hennekam syndrome"@en, "syndrome de Hennekam"@fr ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Hennekam_syndrome>, <https://www.wikidata.org/wiki/Q5714797> ;
  a skos:Concept .

vh8:-G2ZSD47D-B
  skos:prefLabel "pathologie du système lymphatique"@fr, "lymphatic disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-XVNKP097-D .

vh8:-JW4BV3J7-L
  skos:prefLabel "arriération mentale"@fr, "mental retardation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-XVNKP097-D .