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

vh8:-G5Z0J013-D
  skos:prefLabel "hyperaminoacidémie"@fr, "hyperaminoacidemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-FZZ50V0X-L
  skos:prefLabel "hyperalaninémie"@fr, "hyperalaninemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-W790N3DT-N .

vh8:-GTP7G9S9-9
  skos:prefLabel "phenylketonuria"@en, "phénylcétonurie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-KM9H4F3Z-F
  skos:prefLabel "déficit en biotinidase"@fr, "biotidinase deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-LRL4BBDJ-6
  skos:prefLabel "xanthinuria"@en, "xanthinurie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-BMRNNTBL-1
  skos:prefLabel "triméthylaminurie"@fr, "trimethylaminuria"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-M1JJD3BD-K
  skos:prefLabel "alcaptonuria"@en, "alcaptonurie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-N38H9W6C-W
  skos:prefLabel "tyrosinémie"@fr, "tyrosinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-K51XPN9D-J
  skos:prefLabel "déficit en carbamoyl phosphate synthétase"@fr, "carbamoyl phosphate synthetase deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-X616F87X-3
  skos:prefLabel "hyperlysinémie"@fr, "hyperlysinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-J6L96LZW-H
  skos:prefLabel "albinisme"@fr, "albinism"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-NPK6R515-Z
  skos:prefLabel "iminoglycinurie"@fr, "iminoglycinuria"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-PS28SFDC-W
  skos:prefLabel "Hartnup disease"@en, "maladie de Hartnup"@fr ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-CLBZF9F6-1
  skos:prefLabel "cystinosis"@en, "cystinose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-S5WQ640W-R
  skos:prefLabel "homocystinurie"@fr, "homocystinuria"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-XD7X52RB-F
  skos:prefLabel "histidinemia"@en, "histidinémie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-WNDQ9CQ6-S
  skos:prefLabel "leucinose"@fr, "leucinosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-GPLJKM26-H
  skos:prefLabel "hyperargininemia"@en, "hyperargininémie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-MXJQPW9J-9
  skos:prefLabel "hyperornithinémie"@fr, "hyperornithinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-WW4BSM04-9
  skos:prefLabel "hyperprolinurie"@fr, "hyperprolinuria"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-FV653LLM-S
  skos:prefLabel "déficit en ornithine carbamoyltransférase"@fr, "ornithine carbamoyltransferase deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-KWBWN2C4-B
  skos:prefLabel "hyperphénylalaninémie"@fr, "hyperphenylalaninemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-R3PTDNQX-0
  skos:prefLabel "déficit en 3-hydroxy-3-méthylglutaryl-CoA lyase"@fr, "3-hydroxy-3 methylglutaryl-CoA lyase deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-B1QNWJPF-B
  skos:prefLabel "hyperglycinémie"@fr, "hyperglycinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-DJ5S9RM4-R
  skos:prefLabel "déficit en pyruvate carboxylase"@fr, "pyruvate carboxylase deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-V1P90GXQ-F
  skos:prefLabel "hyperhomocystéinémie"@fr, "hyperhomocysteinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-S7WFFBX7-8
  skos:prefLabel "citrullinemia"@en, "citrullinémie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-ZX166L49-N
  skos:prefLabel "hypertyrosinémie"@fr, "hypertyrosinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-L3L6PK7X-D
  skos:prefLabel "hyperaminoacidurie"@fr, "hyperaminoaciduria"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-W70WFX1B-M
  skos:prefLabel "maladie de Joseph"@fr, "Joseph disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-W790N3DT-N
  a skos:Concept ;
  skos:narrower vh8:-ZX166L49-N, vh8:-JL3524N1-R, vh8:-X8BWQ1GV-4, vh8:-L3L6PK7X-D, vh8:-DK45KW8T-C, vh8:-VRPMZTHK-W, vh8:-LWWZCSVG-D, vh8:-G5Z0J013-D, vh8:-PNMG4X6T-4, vh8:-S5WQ640W-R, vh8:-J6L96LZW-H, vh8:-KM9H4F3Z-F, vh8:-PQTWS21G-M, vh8:-LRL4BBDJ-6, vh8:-FZZ50V0X-L, vh8:-N38H9W6C-W, vh8:-R3PTDNQX-0, vh8:-GPLJKM26-H, vh8:-X616F87X-3, vh8:-WNDQ9CQ6-S, vh8:-PS28SFDC-W, vh8:-B1QNWJPF-B, vh8:-W70WFX1B-M, vh8:-K51XPN9D-J, vh8:-LX1M9R8X-J, vh8:-M1JJD3BD-K, vh8:-CLBZF9F6-1, vh8:-QG7Q882K-7, vh8:-MXJQPW9J-9, vh8:-FV653LLM-S, vh8:-V1P90GXQ-F, vh8:-S7WFFBX7-8, vh8:-NPK6R515-Z, vh8:-GTP7G9S9-9, vh8:-WW4BSM04-9, vh8:-V153JK5V-0, vh8:-DJ5S9RM4-R, vh8:-KWBWN2C4-B, vh8:-BMRNNTBL-1, vh8:-XD7X52RB-F ;
  skos:inScheme vh8: ;
  skos:broader vh8:-N32K7HZ8-D, vh8:-G37XWGTK-R ;
  skos:prefLabel "aminoacidopathie"@fr, "aminoacid disorder"@en .

vh8:-VRPMZTHK-W
  skos:prefLabel "hyperméthioninémie"@fr, "hypermethioninemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-V153JK5V-0
  skos:prefLabel "hyperprébêtalipoprotéinémie"@fr, "hyperprebetalipoproteinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-X8BWQ1GV-4
  skos:prefLabel "hypersarcosinémie"@fr, "hypersarcosinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-QG7Q882K-7
  skos:prefLabel "hyperglycinurie"@fr, "hyperglycinuria"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-LX1M9R8X-J
  skos:prefLabel "déficit en biotin-[propionyl-CoA-carboxylase (ATP-hydrolysing)] ligase"@fr, "biotin-[propionyl-CoA-carboxylase (ATP-hydrolysing)] ligase deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-LWWZCSVG-D
  skos:prefLabel "cystinurie"@fr, "cystinuria"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-DK45KW8T-C
  skos:prefLabel "cystathioninuria"@en, "cystathioninurie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-PNMG4X6T-4
  skos:prefLabel "hyperprolinémie"@fr, "hyperprolinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8:-G37XWGTK-R
  skos:prefLabel "enzymopathy"@en, "enzymopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-W790N3DT-N .

vh8:-JL3524N1-R
  skos:prefLabel "syndrome de De Toni-Debré-Fanconi"@fr, "De Toni-Debre-Fanconi syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .

vh8: a skos:ConceptScheme .
vh8:-PQTWS21G-M
  skos:prefLabel "carnosinémie"@fr, "carnosinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-W790N3DT-N .