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

vh8:-Z8TNPKTB-2
  skos:prefLabel "ictère héréditaire de Crigler et Najjar"@fr, "Crigler-Najjar disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-RH1VKSFQ-V
  skos:prefLabel "acatalasémie"@fr, "acatalasemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-Z1VGJVHN-6
  skos:prefLabel "hyperlipoprotéinémie essentielle"@fr, "essential hyperlipoproteinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-MSKR5H7R-L
  skos:prefLabel "maladie"@fr, "disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-G37XWGTK-R .

vh8:-FKQ89NDG-V
  skos:prefLabel "maladie de l'oeil de poisson"@fr, "fish-eye disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-DF27RSF5-D
  skos:prefLabel "hyperoxalurie"@fr, "hyperoxaluria"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-HKHNT5BS-P
  skos:prefLabel "glycogenosis"@en, "glycogénose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-WWVN4096-B
  skos:prefLabel "Wolman disease"@en, "maladie de Wolman"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-VHSZS195-R
  skos:prefLabel "cerebrotendinous xanthomatosis"@en, "xanthomatose cérébrotendineuse"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-WQHMLFJJ-0
  skos:prefLabel "syndrome de Lowe"@fr, "Lowe syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-SPNL2Z1Z-P
  skos:prefLabel "abêtalipoprotéinémie"@fr, "abetalipoproteinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-XD7X52RB-F
  skos:prefLabel "histidinemia"@en, "histidinémie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-PJQJX191-B
  skos:prefLabel "syndrome des glycoprotéines déficientes en hydrates de carbone"@fr, "carbohydrate deficient glycoprotein syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-B3BK074Z-V
  skos:prefLabel "maladie de Wilson"@fr, "Wilson disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-C2L49H54-K
  skos:prefLabel "fructosurie"@fr, "fructosuria"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-PTFCD7X4-4
  skos:prefLabel "myopathie mitochondriale"@fr, "mitochondrial myopathy"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-MTJ4WC97-3
  skos:prefLabel "mitochondrial disease"@en, "cytopathie mitochondriale"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-PRSSL1XP-5
  skos:prefLabel "thésaurismose"@fr, "storage disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-L0BXS7Z7-C
  skos:prefLabel "protoporphyrie"@fr, "protoporphyria"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-LLM7LN8S-W
  skos:prefLabel "néphrosialidose"@fr, "nephrosialidosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-H65V5PX7-9
  skos:prefLabel "hypophosphatasie"@fr, "hypophosphatasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-H2B6QNR7-B
  skos:prefLabel "porphyrie"@fr, "porphyria"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-D48QVGJZ-0
  skos:prefLabel "fructosemia"@en, "fructosémie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-FHDLVS0M-7
  skos:prefLabel "alpha-1 antitrypsin deficiency"@en, "déficit en alpha-1 antitrypsine"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-W790N3DT-N
  skos:prefLabel "aminoacid disorder"@en, "aminoacidopathie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-RPL8R9P9-Z
  skos:prefLabel "lysosomal storage disease"@en, "pathologie des lysosomes"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-PLPSC0WL-4
  skos:prefLabel "oxalose"@fr, "oxalosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-WK6210CD-T
  skos:prefLabel "Menkes syndrome"@en, "syndrome de Menkes"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-QB7RMT32-K
  skos:prefLabel "adenosine deaminase deficiency"@en, "déficit en adénosine désaminase"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-NLJ9SXMF-5
  skos:prefLabel "maladie de Refsum"@fr, "Refsum disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-WCRT6QVG-G
  skos:prefLabel "fucosidose"@fr, "fucosidosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-QQKF2GK3-J
  skos:prefLabel "syndrome d'excès apparent de minéralocorticoïde"@fr, "apparent mineralocorticoid excess syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-MGG0QRPT-S
  skos:prefLabel "pyruvate kinase deficiency"@en, "déficit en pyruvate kinase"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-Z2B6G9GP-W
  skos:prefLabel "acidémie isovalérique"@fr, "isovaleric acidemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-ZQTHM36F-K
  skos:prefLabel "dysplasie hématodiaphysaire de Ghosal"@fr, "diaphyseal dysplasia with anemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-M8W0T5JK-9
  skos:prefLabel "mucolipidose"@fr, "mucolipidosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-CRQ2TNWZ-K
  skos:prefLabel "galactosemia"@en, "galactosémie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-GF8SW923-W
  skos:prefLabel "erythropoietic protoporphyria"@en, "protoporphyrie érythropoïétique"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-L6N8134K-9
  skos:prefLabel "glucose-6-phosphate dehydrogenase deficiency"@en, "déficit en glucose-6-phosphate déshydrogénase"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-NZNJ4N5X-1
  skos:prefLabel "déficit en hypoxanthine-guanine phosphoribosyltransférase"@fr, "hypoxanthine-guanine phosphoribosyltransferase deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-HJ0D3XSC-S
  skos:prefLabel "déficit en carnitine palmitoyltransférase"@fr, "carnitine O-palmitoyltransferase deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-CQM6Q5MM-P
  skos:prefLabel "hypercuprémie"@fr, "hypercupremia"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-RVZ3P800-W
  skos:prefLabel "syndrome de Lesh et Nyhan"@fr, "Lesch-Nyhan syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-DSV7960J-H
  skos:prefLabel "déficit en acyl-CoA déshydrogénase"@fr, "acyl-CoA dehydrogenase deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-G37XWGTK-R
  skos:narrower vh8:-HQVVF9T2-C, vh8:-C2L49H54-K, vh8:-WQHMLFJJ-0, vh8:-H65V5PX7-9, vh8:-PTFCD7X4-4, vh8:-DF27RSF5-D, vh8:-W790N3DT-N, vh8:-CRQ2TNWZ-K, vh8:-F7XJ1KPX-R, vh8:-G5MZL975-B, vh8:-NZNJ4N5X-1, vh8:-L6N8134K-9, vh8:-MGG0QRPT-S, vh8:-WWVN4096-B, vh8:-HJ0D3XSC-S, vh8:-B3BK074Z-V, vh8:-Z8TNPKTB-2, vh8:-XD7X52RB-F, vh8:-RVZ3P800-W, vh8:-QQKF2GK3-J, vh8:-PJQJX191-B, vh8:-VHSZS195-R, vh8:-NLJ9SXMF-5, vh8:-JG6GHJDH-F, vh8:-PLPSC0WL-4, vh8:-DSV7960J-H, vh8:-M8W0T5JK-9, vh8:-MTJ4WC97-3, vh8:-RPL8R9P9-Z, vh8:-FKQ89NDG-V, vh8:-Z2B6G9GP-W, vh8:-LLM7LN8S-W, vh8:-WK6210CD-T, vh8:-SPNL2Z1Z-P, vh8:-L0BXS7Z7-C, vh8:-HKHNT5BS-P, vh8:-CQM6Q5MM-P, vh8:-ZQTHM36F-K, vh8:-H2B6QNR7-B, vh8:-QB7RMT32-K, vh8:-GF8SW923-W, vh8:-Z1VGJVHN-6, vh8:-ZXDHHJBR-6, vh8:-XBJ2RJ3G-X, vh8:-PRSSL1XP-5, vh8:-D48QVGJZ-0, vh8:-WCRT6QVG-G, vh8:-RH1VKSFQ-V, vh8:-FHDLVS0M-7 ;
  skos:inScheme vh8: ;
  skos:broader vh8:-MSKR5H7R-L ;
  skos:prefLabel "enzymopathie"@fr, "enzymopathy"@en ;
  a skos:Concept ;
  skos:exactMatch <https://fr.wikipedia.org/wiki/Enzymopathie> ;
  skos:definition "Une enzymopathie est une maladie héréditaire attribuable à un déficit enzymatique. (Wikipédia)"@fr .

vh8:-HQVVF9T2-C
  skos:prefLabel "neuronal ceroid lipofuscinosis"@en, "céroïde lipofuscinose neuronale"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-XBJ2RJ3G-X
  skos:prefLabel "mucopolysaccharidosis"@en, "mucopolysaccharidose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-G5MZL975-B
  skos:prefLabel "atrophia gyrata"@fr, "atrophia gyrata"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8: a skos:ConceptScheme .
vh8:-F7XJ1KPX-R
  skos:prefLabel "sphingolipidosis"@en, "sphingolipidose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-ZXDHHJBR-6
  skos:prefLabel "lipofuscinose"@fr, "lipofuscinosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .

vh8:-JG6GHJDH-F
  skos:prefLabel "syndrome d'hyperplasie congénitale de la surrénale"@fr, "congenital adrenal hyperplasia syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-G37XWGTK-R .