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

vh8:-TXJKBRFW-2
  skos:prefLabel "syndrome de Coffin et Siris"@fr, "Coffin-Siris syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-M91FVLZ5-3
  skos:prefLabel "hypoplasie dermique en aires"@fr, "focal dermal hypoplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-N5XDC60G-5
  skos:prefLabel "acrocéphalosyndactylie"@fr, "acrocephalosyndactylia"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-D0Q0Z4Q7-7
  skos:prefLabel "dysostose fronto-facio-nasale"@fr, "oculoauriculofrontonasal syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-X43ZHQLR-L
  skos:prefLabel "Holt-Oram syndrome"@en, "syndrome de Holt-Oram"@fr ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-K74MDW6H-R
  skos:prefLabel "craniosynostose"@fr, "craniosynostosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-VRW6TJKT-W
  skos:prefLabel "Crouzon disease"@en, "dysostose crâniofaciale de Crouzon"@fr ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-KV8X04B5-9
  skos:prefLabel "Goldenhar syndrome"@en, "dysplasie oculoauriculovertébrale de Goldenhar"@fr ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-QSWWWSHX-W
  skos:prefLabel "dysostose orodigitofaciale"@fr, "orofaciodigital syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-MNNB8B9S-4
  skos:prefLabel "Sprengel's deformity"@en, "surélévation congénitale de l'omoplate"@fr ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-D4VR1G17-D
  skos:prefLabel "Klippel-Feil syndrome"@en, "syndrome de Klippel-Feil"@fr ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-BSFBPL4W-S
  skos:prefLabel "diseases of the osteoarticular system"@en, "pathologie du système ostéoarticulaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-H707N75F-8 .

vh8:-QF166PD6-3
  skos:prefLabel "syndactylie"@fr, "syndactyly"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-ZTQ66C9Q-S
  skos:prefLabel "polydactylie"@fr, "polydactyly"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-FZ8ZHWR3-3
  skos:prefLabel "syndrome de Poland"@fr, "Poland syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-X6PZ6KSL-3
  skos:prefLabel "syndrome cérébrocostomandibulaire"@fr, "cerebrocostomandibular syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-RM7L6Z6J-L
  skos:prefLabel "Shwachman-Diamond syndrome"@en, "syndrome de Shwachman-Diamond"@fr ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-B75HKZZG-F
  skos:prefLabel "ostéoonychodysostose"@fr, "nail patella syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-K17D2MN5-2
  skos:prefLabel "synostose multiple"@fr, "multiple synostosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-DBNLLTMT-K
  skos:prefLabel "tétraphocomélie"@fr, "tetraphocomelia"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-K52TXF4H-M
  skos:prefLabel "Hanhart syndrome"@en, "syndrome de Hanhart"@fr ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8: a skos:ConceptScheme .
vh8:-CLPLGJNP-V
  skos:prefLabel "microsomie hémifaciale"@fr, "hemifacial microsomia"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-BC56H2HC-P
  skos:prefLabel "spondylocostal dysostosis"@en, "dysostose spondylocostale"@fr ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-F8BNBFKN-6
  skos:prefLabel "syndrome de Mohr"@fr, "Mohr syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-JXFTVRM3-6
  skos:prefLabel "dysostose acrofaciale de Nager"@fr, "Nager acrofacial dysostosis syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-KSS0VVWV-B
  skos:prefLabel "dysostose mandibulofaciale"@fr, "mandibulofacial dysostosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .

vh8:-H707N75F-8
  skos:narrower vh8:-JXFTVRM3-6, vh8:-M91FVLZ5-3, vh8:-TXJKBRFW-2, vh8:-K74MDW6H-R, vh8:-QF166PD6-3, vh8:-KV8X04B5-9, vh8:-D4VR1G17-D, vh8:-RM7L6Z6J-L, vh8:-B75HKZZG-F, vh8:-VRW6TJKT-W, vh8:-K52TXF4H-M, vh8:-ZTQ66C9Q-S, vh8:-KSS0VVWV-B, vh8:-FZ8ZHWR3-3, vh8:-BC56H2HC-P, vh8:-D0Q0Z4Q7-7, vh8:-X6PZ6KSL-3, vh8:-CLPLGJNP-V, vh8:-QSWWWSHX-W, vh8:-DBNLLTMT-K, vh8:-FRHTZJFN-6, vh8:-N5XDC60G-5, vh8:-MNNB8B9S-4, vh8:-F8BNBFKN-6, vh8:-X43ZHQLR-L, vh8:-K17D2MN5-2 ;
  a skos:Concept ;
  skos:prefLabel "dysostosis"@en, "dysostose"@fr ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Dysostosis> ;
  skos:inScheme vh8: ;
  skos:definition "A dysostosis is a disorder of the development of bone, in particular affecting ossification.Examples include craniofacial dysostosis, Klippel–Feil syndrome, and Rubinstein–Taybi syndrome. (Wikipedia)"@en ;
  skos:broader vh8:-F0Q8HP18-R, vh8:-BSFBPL4W-S .

vh8:-F0Q8HP18-R
  skos:prefLabel "malformation"@fr, "malformation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-H707N75F-8 .

vh8:-FRHTZJFN-6
  skos:prefLabel "symphalangie"@fr, "symphalangism"@en ;
  a skos:Concept ;
  skos:broader vh8:-H707N75F-8 .