@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:-PLFNN4S2-4 .

vh8:-J96QZPNL-5
  skos:prefLabel "sidéropénie"@fr, "sideropenia"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-Z7HB6W2K-N
  skos:prefLabel "hyperuricémie"@fr, "hyperuricemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-MSKR5H7R-L
  skos:prefLabel "maladie"@fr, "disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-PLFNN4S2-4 .

vh8:-FKQ89NDG-V
  skos:prefLabel "maladie de l'oeil de poisson"@fr, "fish-eye disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-RLKSQ0S9-J
  skos:prefLabel "hyperinsulinémie"@fr, "hyperinsulinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-THM4F0QM-M
  skos:prefLabel "lipoïdose"@fr, "lipoidosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-S20F6PN1-S
  skos:prefLabel "scléroedème de Buschke"@fr, "scleredema of Buschke"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-FRXLBGVG-F
  skos:prefLabel "rachitisme vitaminorésistant"@fr, "vitamin-resistant rickets"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-F493ZZC4-8
  skos:prefLabel "insulin resistance"@en, "insulinorésistance"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-NNL526RR-H
  skos:prefLabel "familial amyloidotic polyneuropathy type 1"@en, "polyneuropathie amyloïde familiale de type 1"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

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:-PLFNN4S2-4 .

vh8:-B3BK074Z-V
  skos:prefLabel "maladie de Wilson"@fr, "Wilson disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-P5X7C1GC-0
  skos:prefLabel "hyalinosis cutis et mucosae"@en, "hyalinose cutanéomuqueuse"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-DQB3F9P9-J
  skos:prefLabel "flapping tremor"@fr, "flapping tremor"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-HWJZV7N8-9
  skos:prefLabel "syndrome métabolique"@fr, "metabolic syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-FS5SQ9X8-V
  skos:prefLabel "dyslipémie"@fr, "dyslipemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-NM3KPZ36-3
  skos:prefLabel "syndrome de Sjögren et Larsson"@fr, "Sjögren-Larsson syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-PTFCD7X4-4
  skos:prefLabel "myopathie mitochondriale"@fr, "mitochondrial myopathy"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-CJDK6N2N-P
  skos:prefLabel "hémosidérose"@fr, "hemosiderosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-FJSS9D5C-3
  skos:prefLabel "xanthelasma"@en, "xanthélasma"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-DRX308X0-8
  skos:prefLabel "hypocuprémie"@fr, "hypocupremia"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-LLM7LN8S-W
  skos:prefLabel "néphrosialidose"@fr, "nephrosialidosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-X901MQNZ-M
  skos:prefLabel "hypersidérémie"@fr, "hypersideremia"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-H2B6QNR7-B
  skos:prefLabel "porphyrie"@fr, "porphyria"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-KQ77D01G-M
  skos:prefLabel "amyloidosis"@en, "amyloïdose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-RPL8R9P9-Z
  skos:prefLabel "lysosomal storage disease"@en, "pathologie des lysosomes"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-PLPSC0WL-4
  skos:prefLabel "oxalose"@fr, "oxalosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-PLFNN4S2-4
  skos:definition "Une maladie métabolique est un trouble médical qui affecte les métabolismes dans la cellule, en particulier la production d'énergie. (Wikipédia)"@fr ;
  skos:narrower vh8:-CJDK6N2N-P, vh8:-X2BWKCJW-M, vh8:-ZG9NH0MB-2, vh8:-QZGXZRM9-2, vh8:-PTFCD7X4-4, vh8:-D3LLNXF7-M, vh8:-H5M50Z9W-H, vh8:-PLPSC0WL-4, vh8:-J96QZPNL-5, vh8:-L0JL9X6F-K, vh8:-B3BK074Z-V, vh8:-LLM7LN8S-W, vh8:-T33HR75Z-G, vh8:-D6XMQL01-N, vh8:-P5X7C1GC-0, vh8:-PJQJX191-B, vh8:-KL5C1VTL-Q, vh8:-FRXLBGVG-F, vh8:-DQB3F9P9-J, vh8:-Z7HB6W2K-N, vh8:-RLKSQ0S9-J, vh8:-NNL526RR-H, vh8:-Z8TNPKTB-2, vh8:-JG6GHJDH-F, vh8:-H2B6QNR7-B, vh8:-XBJ2RJ3G-X, vh8:-KQ77D01G-M, vh8:-RPL8R9P9-Z, vh8:-JDNXV8R3-5, vh8:-FJSS9D5C-3, vh8:-NRD7KTTB-N, vh8:-LNX6FP4S-7, vh8:-FS5SQ9X8-V, vh8:-S20F6PN1-S, vh8:-QQKF2GK3-J, vh8:-M8W0T5JK-9, vh8:-R2PS9LZZ-S, vh8:-SC0DL7FZ-9, vh8:-GF8SW923-W, vh8:-HWJZV7N8-9, vh8:-LQV5ZDCJ-D, vh8:-FKQ89NDG-V, vh8:-FG7ML2RD-K, vh8:-CX829SPQ-C, vh8:-DRX308X0-8, vh8:-X901MQNZ-M, vh8:-THM4F0QM-M, vh8:-F493ZZC4-8, vh8:-NM3KPZ36-3, vh8:-F248T5T7-W ;
  skos:exactMatch <https://fr.wikipedia.org/wiki/Maladie_m%C3%A9tabolique> ;
  skos:broader vh8:-MSKR5H7R-L ;
  skos:inScheme vh8: ;
  skos:prefLabel "metabolic diseases"@en, "maladie métabolique"@fr ;
  a skos:Concept .

vh8:-X2BWKCJW-M
  skos:prefLabel "hemochromatosis type 1"@en, "hémochomatose de type 1"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-JDNXV8R3-5
  skos:prefLabel "diabetes mellitus type 2"@en, "diabète de type 2"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-LNX6FP4S-7
  skos:prefLabel "hypocéruloplasminémie"@fr, "hypoceruloplasminemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-QQKF2GK3-J
  skos:prefLabel "syndrome d'excès apparent de minéralocorticoïde"@fr, "apparent mineralocorticoid excess syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-SC0DL7FZ-9
  skos:prefLabel "ictère héréditaire de Dubin-Johnson"@fr, "Dubin-Johnson disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-R2PS9LZZ-S
  skos:prefLabel "carnitine deficiency"@en, "déficit en carnitine"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-M8W0T5JK-9
  skos:prefLabel "mucolipidose"@fr, "mucolipidosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-QZGXZRM9-2
  skos:prefLabel "mucoviscidose"@fr, "cystic fibrosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-D6XMQL01-N
  skos:prefLabel "desmostérolose"@fr, "desmosterolosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-KL5C1VTL-Q
  skos:prefLabel "mucinosis"@en, "mucinose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-H5M50Z9W-H
  skos:prefLabel "calcinose"@fr, "calcinosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-GF8SW923-W
  skos:prefLabel "erythropoietic protoporphyria"@en, "protoporphyrie érythropoïétique"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-LQV5ZDCJ-D
  skos:prefLabel "food intolerance"@en, "intolérance alimentaire"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-CX829SPQ-C
  skos:prefLabel "Barth syndrome"@en, "syndrome de Barth"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-NRD7KTTB-N
  skos:prefLabel "surcharge en fer"@fr, "iron overload"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-XBJ2RJ3G-X
  skos:prefLabel "mucopolysaccharidosis"@en, "mucopolysaccharidose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-F248T5T7-W
  skos:prefLabel "rachitisme vitaminodépendant"@fr, "vitamin D-dependent rickets"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-FG7ML2RD-K
  skos:prefLabel "homocitrullinurie"@fr, "homocitrullinuria"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8: a skos:ConceptScheme .
vh8:-L0JL9X6F-K
  skos:prefLabel "Dorfman-Chanarin syndrome"@en, "syndrome de Dorfman-Chanarin"@fr ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-ZG9NH0MB-2
  skos:prefLabel "pathologie des peroxysomes"@fr, "peroxisomal disorders"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-T33HR75Z-G
  skos:prefLabel "trichothiodystrophie"@fr, "trichothiodystrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-D3LLNXF7-M
  skos:prefLabel "xanthome"@fr, "xanthoma"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .

vh8:-JG6GHJDH-F
  skos:prefLabel "syndrome d'hyperplasie congénitale de la surrénale"@fr, "congenital adrenal hyperplasia syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-PLFNN4S2-4 .