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'en:ornithine carbamoyltransferase deficiency disease'
(id=6818707 ; fe=en:ornithine carbamoyltransferase deficiency disease ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=39574.54998779297 creation date=2017-06-25 touchdate=2025-08-13 23:53:07.000)
≈ 574 relations sortantes

  1. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 43 / 1 -> en:hepatic ornithine transcarbamylase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hepatic ornithine transcarbamylase deficiency | rel=r_associated | relid=0 | w=43
  2. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 43 / 1 -> en:psychology qualifier
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:psychology qualifier | rel=r_associated | relid=0 | w=43
  3. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 42 / 0.977 -> en:disorder of amino acid and organic acid metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:disorder of amino acid and organic acid metabolism | rel=r_associated | relid=0 | w=42
  4. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 42 / 0.977 -> en:disorder of creatine synthesis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:disorder of creatine synthesis | rel=r_associated | relid=0 | w=42
  5. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 42 / 0.977 -> en:mental retardation
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:mental retardation | rel=r_associated | relid=0 | w=42
  6. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 42 / 0.977 -> en:pentosuria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:pentosuria | rel=r_associated | relid=0 | w=42
  7. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 41 / 0.953 -> en:allan-herndon-dudley syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:allan-herndon-dudley syndrome | rel=r_associated | relid=0 | w=41
  8. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 41 / 0.953 -> en:biotinidase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=41
  9. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 41 / 0.953 -> en:simpson golabi behmel syndrome type 1
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:simpson golabi behmel syndrome type 1 | rel=r_associated | relid=0 | w=41
  10. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 40 / 0.93 -> en:disorder of branched-chain amino acid metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:disorder of branched-chain amino acid metabolism | rel=r_associated | relid=0 | w=40
  11. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 39 / 0.907 -> en:cytochrome-c oxidase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=39
  12. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 39 / 0.907 -> en:disorder of aromatic amino acid metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:disorder of aromatic amino acid metabolism | rel=r_associated | relid=0 | w=39
  13. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 39 / 0.907 -> en:inherited disorder of bilirubin metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:inherited disorder of bilirubin metabolism | rel=r_associated | relid=0 | w=39
  14. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 39 / 0.907 -> en:methylmalonic acidemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:methylmalonic acidemia | rel=r_associated | relid=0 | w=39
  15. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 38 / 0.884 -> en:5' 10' methylenetetrahydrofolate reductase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:5' 10' methylenetetrahydrofolate reductase deficiency | rel=r_associated | relid=0 | w=38
  16. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the ornithine transcarbamylase gene (otc, 311250.0001)
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:caused by mutation in the ornithine transcarbamylase gene (otc, 311250.0001) | rel=r_associated | relid=0 | w=38
  17. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 38 / 0.884 -> en:glucose-6-phosphate dehydrogenase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glucose-6-phosphate dehydrogenase deficiency | rel=r_associated | relid=0 | w=38
  18. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 38 / 0.884 -> en:hemophilia b
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hemophilia b | rel=r_associated | relid=0 | w=38
  19. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 38 / 0.884 -> en:primary hyperoxaluria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:primary hyperoxaluria | rel=r_associated | relid=0 | w=38
  20. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 36 / 0.837 -> carence en ornithine carbamoyltransférase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=carence en ornithine carbamoyltransférase | rel=r_associated | relid=0 | w=36
  21. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 36 / 0.837 -> en:carnitine palmitoyltransferase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:carnitine palmitoyltransferase deficiency | rel=r_associated | relid=0 | w=36
  22. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 36 / 0.837 -> en:holocarboxylase synthetase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:holocarboxylase synthetase deficiency | rel=r_associated | relid=0 | w=36
  23. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 36 / 0.837 -> en:lesch-nyhan syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=36
  24. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 36 / 0.837 -> en:n-acetylglutamate synthase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=36
  25. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 36 / 0.837 -> en:x-linked lissencephaly
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked lissencephaly | rel=r_associated | relid=0 | w=36
  26. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> déficit en ornithine transcarbamylase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=déficit en ornithine transcarbamylase | rel=r_associated | relid=0 | w=35
  27. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:amino acid metabolism disorder
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:amino acid metabolism disorder | rel=r_associated | relid=0 | w=35
  28. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:androgen insensitivity syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:androgen insensitivity syndrome | rel=r_associated | relid=0 | w=35
  29. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:arginosuccinate lyase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:arginosuccinate lyase deficiency | rel=r_associated | relid=0 | w=35
  30. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:borjeson-forssman-lehmann syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:borjeson-forssman-lehmann syndrome | rel=r_associated | relid=0 | w=35
  31. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:childhood hypophosphatasia (disorder)
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  32. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:circulating enzyme deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:circulating enzyme deficiency | rel=r_associated | relid=0 | w=35
  33. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:citrullinemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:citrullinemia | rel=r_associated | relid=0 | w=35
  34. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:deficiency of fructokinase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:deficiency of fructokinase | rel=r_associated | relid=0 | w=35
  35. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:deficiency of steryl-sulfatase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:deficiency of steryl-sulfatase | rel=r_associated | relid=0 | w=35
  36. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:disorder of histidine metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:disorder of histidine metabolism | rel=r_associated | relid=0 | w=35
  37. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:dmd-associated dilated cardiomyopathy
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:dmd-associated dilated cardiomyopathy | rel=r_associated | relid=0 | w=35
  38. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:ethanolaminosis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ethanolaminosis | rel=r_associated | relid=0 | w=35
  39. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:gamma-glutamyltransferase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:gamma-glutamyltransferase deficiency | rel=r_associated | relid=0 | w=35
  40. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:hereditary xanthinuria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hereditary xanthinuria | rel=r_associated | relid=0 | w=35
  41. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | rel=r_associated | relid=0 | w=35
  42. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:hyperprolinemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperprolinemia | rel=r_associated | relid=0 | w=35
  43. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:in urine
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:in urine | rel=r_associated | relid=0 | w=35
  44. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:inherited disorder of folate metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:inherited disorder of folate metabolism | rel=r_associated | relid=0 | w=35
  45. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:lecithin acyltransferase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:lecithin acyltransferase deficiency | rel=r_associated | relid=0 | w=35
  46. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:lethargy
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:lethargy | rel=r_associated | relid=0 | w=35
  47. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:lipid metabolism disorder
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:lipid metabolism disorder | rel=r_associated | relid=0 | w=35
  48. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:lipoid congenital adrenal hyperplasia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:lipoid congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=35
  49. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:lujan fryns syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:lujan fryns syndrome | rel=r_associated | relid=0 | w=35
  50. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:maple syrup urine disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=35
  51. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:methylene thf reductase deficiency and homocystinuria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:methylene thf reductase deficiency and homocystinuria | rel=r_associated | relid=0 | w=35
  52. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:microbiological
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:microbiological | rel=r_associated | relid=0 | w=35
  53. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:norrie syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:norrie syndrome | rel=r_associated | relid=0 | w=35
  54. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:otc, arg245trp
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, arg245trp | rel=r_associated | relid=0 | w=35
  55. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:otc, ivs2, g-a, -1
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, ivs2, g-a, -1 | rel=r_associated | relid=0 | w=35
  56. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:otc, tyr313asp
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, tyr313asp | rel=r_associated | relid=0 | w=35
  57. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:other specified disorders of amino-acid metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:other specified disorders of amino-acid metabolism | rel=r_associated | relid=0 | w=35
  58. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:partington x-linked mental retardation syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:partington x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=35
  59. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:phenylketonuria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:phenylketonuria | rel=r_associated | relid=0 | w=35
  60. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:porphobilinogen synthase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:porphobilinogen synthase deficiency | rel=r_associated | relid=0 | w=35
  61. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:protein avoidance
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:protein avoidance | rel=r_associated | relid=0 | w=35
  62. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:pyruvate dehydrogenase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:pyruvate dehydrogenase deficiency | rel=r_associated | relid=0 | w=35
  63. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:radiotherapeutic
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:radiotherapeutic | rel=r_associated | relid=0 | w=35
  64. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:rehabilitation aspects
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:rehabilitation aspects | rel=r_associated | relid=0 | w=35
  65. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:therapeutic aspects
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:therapeutic aspects | rel=r_associated | relid=0 | w=35
  66. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:x-linked creatine transporter deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked creatine transporter deficiency | rel=r_associated | relid=0 | w=35
  67. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:x-linked recessive
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked recessive | rel=r_associated | relid=0 | w=35
  68. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 35 / 0.814 -> en:x-linked severe combined immunodeficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked severe combined immunodeficiency | rel=r_associated | relid=0 | w=35
  69. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> déficit en ornithine-carbamyl-transférase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=déficit en ornithine-carbamyl-transférase | rel=r_associated | relid=0 | w=34
  70. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:2-hydroxyglutaric aciduria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=34
  71. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:5 alpha steroid reductase 2 deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=34
  72. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:amino acid transport disorders, inborn
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:amino acid transport disorders, inborn | rel=r_associated | relid=0 | w=34
  73. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:anhidrotic ectodermal dysplasia 1
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:anhidrotic ectodermal dysplasia 1 | rel=r_associated | relid=0 | w=34
  74. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:argininosuccinic aciduria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=34
  75. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:aspects of radionuclide imaging
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:aspects of radionuclide imaging | rel=r_associated | relid=0 | w=34
  76. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:brain diseases, metabolic, inborn
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:brain diseases, metabolic, inborn | rel=r_associated | relid=0 | w=34
  77. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:brunner syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:brunner syndrome | rel=r_associated | relid=0 | w=34
  78. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:carbamoyl-phosphate synthetase i deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:carbamoyl-phosphate synthetase i deficiency | rel=r_associated | relid=0 | w=34
  79. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:childhood cerebral x-linked adrenoleukodystrophy
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:childhood cerebral x-linked adrenoleukodystrophy | rel=r_associated | relid=0 | w=34
  80. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:conditions tested for in this newborn screening study:id:pt:bld.dot:nom
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:conditions tested for in this newborn screening study:id:pt:bld.dot:nom | rel=r_associated | relid=0 | w=34
  81. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:congenital
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:congenital | rel=r_associated | relid=0 | w=34
  82. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:defect in post-translational modification of lysosomal enzymes
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:defect in post-translational modification of lysosomal enzymes | rel=r_associated | relid=0 | w=34
  83. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:dihydropyrimidinase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:dihydropyrimidinase deficiency | rel=r_associated | relid=0 | w=34
  84. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:epidemiologic
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:epidemiologic | rel=r_associated | relid=0 | w=34
  85. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:ethnologic
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ethnologic | rel=r_associated | relid=0 | w=34
  86. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:fragile x syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=34
  87. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:fructose-1,6-bisphosphatase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:fructose-1,6-bisphosphatase deficiency | rel=r_associated | relid=0 | w=34
  88. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:gaucher disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:gaucher disease | rel=r_associated | relid=0 | w=34
  89. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:glutamate formiminotransferase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glutamate formiminotransferase deficiency | rel=r_associated | relid=0 | w=34
  90. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:glutaric acidemia type 1
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glutaric acidemia type 1 | rel=r_associated | relid=0 | w=34
  91. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:glutathione synthetase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glutathione synthetase deficiency | rel=r_associated | relid=0 | w=34
  92. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:glycogen storage disease type x
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glycogen storage disease type x | rel=r_associated | relid=0 | w=34
  93. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:high urinary orotic acid
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:high urinary orotic acid | rel=r_associated | relid=0 | w=34
  94. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:histidinemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:histidinemia | rel=r_associated | relid=0 | w=34
  95. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:hyperglutaminemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperglutaminemia | rel=r_associated | relid=0 | w=34
  96. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:hyperglycinemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperglycinemia | rel=r_associated | relid=0 | w=34
  97. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:hyperphenylalaninemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperphenylalaninemia | rel=r_associated | relid=0 | w=34
  98. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:in blood
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:in blood | rel=r_associated | relid=0 | w=34
  99. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:inborn errors of steroid synthesis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:inborn errors of steroid synthesis | rel=r_associated | relid=0 | w=34
  100. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:lactose intolerance, adult type
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:lactose intolerance, adult type | rel=r_associated | relid=0 | w=34
  101. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:low plasma arginine
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:low plasma arginine | rel=r_associated | relid=0 | w=34
  102. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:mental retardation with psychosis, pyramidal signs, and macroorchidism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:mental retardation with psychosis, pyramidal signs, and macroorchidism | rel=r_associated | relid=0 | w=34
  103. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:metabolic aspects
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:metabolic aspects | rel=r_associated | relid=0 | w=34
  104. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:methylcrotonyl-coa carboxylase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:methylcrotonyl-coa carboxylase deficiency | rel=r_associated | relid=0 | w=34
  105. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:methylmalonyl-coenzyme a mutase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:methylmalonyl-coenzyme a mutase deficiency | rel=r_associated | relid=0 | w=34
  106. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:microphthalmia, syndromic 1
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:microphthalmia, syndromic 1 | rel=r_associated | relid=0 | w=34
  107. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:ohdo syndrome, maat-kievit-brunner type
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ohdo syndrome, maat-kievit-brunner type | rel=r_associated | relid=0 | w=34
  108. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:otc, 1-bp del, 403g
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, 1-bp del, 403g | rel=r_associated | relid=0 | w=34
  109. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:otc, leu148phe
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, leu148phe | rel=r_associated | relid=0 | w=34
  110. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:pelizaeus-merzbacher disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:pelizaeus-merzbacher disease | rel=r_associated | relid=0 | w=34
  111. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:seizure
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:seizure | rel=r_associated | relid=0 | w=34
  112. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:spondyloepiphyseal dysplasia tarda, x-linked
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:spondyloepiphyseal dysplasia tarda, x-linked | rel=r_associated | relid=0 | w=34
  113. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:succinic semialdehyde dehydrogenase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:succinic semialdehyde dehydrogenase deficiency | rel=r_associated | relid=0 | w=34
  114. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:tyrosinemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:tyrosinemia | rel=r_associated | relid=0 | w=34
  115. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:urocanase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:urocanase deficiency | rel=r_associated | relid=0 | w=34
  116. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:x-linked epilepsy with learning disability and behavior disorder syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked epilepsy with learning disability and behavior disorder syndrome | rel=r_associated | relid=0 | w=34
  117. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:x-linked hydrocephalus syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked hydrocephalus syndrome | rel=r_associated | relid=0 | w=34
  118. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 34 / 0.791 -> en:x-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia | rel=r_associated | relid=0 | w=34
  119. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:17 alpha-hydroxyprogesterone aldolase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:17 alpha-hydroxyprogesterone aldolase deficiency | rel=r_associated | relid=0 | w=32
  120. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:acyl-coa dehydrogenase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=32
  121. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:adolescent x-linked adrenoleukodystrophy
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:adolescent x-linked adrenoleukodystrophy | rel=r_associated | relid=0 | w=32
  122. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:adrenal gland hyperplasia ii
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:adrenal gland hyperplasia ii | rel=r_associated | relid=0 | w=32
  123. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:alkaptonuria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=32
  124. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:amino acidemia disorder suspected:prid:pt:bld.dot:nom
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:amino acidemia disorder suspected:prid:pt:bld.dot:nom | rel=r_associated | relid=0 | w=32
  125. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:argininemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:argininemia | rel=r_associated | relid=0 | w=32
  126. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:ataxia, fatal x-linked, with deafness and loss of vision
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ataxia, fatal x-linked, with deafness and loss of vision | rel=r_associated | relid=0 | w=32
  127. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:clinical spectrum in males ranges from lethal neonatal onset to milder forms with first recognized episode in late childhood or even in adulthood
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:clinical spectrum in males ranges from lethal neonatal onset to milder forms with first recognized episode in late childhood or even in adulthood | rel=r_associated | relid=0 | w=32
  128. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:coma
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:coma | rel=r_associated | relid=0 | w=32
  129. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism | rel=r_associated | relid=0 | w=32
  130. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:congenital pancreatic enterokinase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:congenital pancreatic enterokinase deficiency | rel=r_associated | relid=0 | w=32
  131. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:disorder of glycosaminoglycan metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:disorder of glycosaminoglycan metabolism | rel=r_associated | relid=0 | w=32
  132. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:dyserythropoietic anemia with thrombocytopenia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:dyserythropoietic anemia with thrombocytopenia | rel=r_associated | relid=0 | w=32
  133. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:enzymology
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:enzymology | rel=r_associated | relid=0 | w=32
  134. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:episodic ataxia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:episodic ataxia | rel=r_associated | relid=0 | w=32
  135. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:erythropoietic protoporphyria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:erythropoietic protoporphyria | rel=r_associated | relid=0 | w=32
  136. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:hereditary fructose intolerance
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=32
  137. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:hunter syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hunter syndrome | rel=r_associated | relid=0 | w=32
  138. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:hydrocephalus with cerebellar agenesis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hydrocephalus with cerebellar agenesis | rel=r_associated | relid=0 | w=32
  139. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:isolated noncompaction of the ventricular myocardium
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:isolated noncompaction of the ventricular myocardium | rel=r_associated | relid=0 | w=32
  140. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:isovaleric acidemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:isovaleric acidemia | rel=r_associated | relid=0 | w=32
  141. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:lipid metabolism, inborn errors
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:lipid metabolism, inborn errors | rel=r_associated | relid=0 | w=32
  142. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:low plasma citrulline
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:low plasma citrulline | rel=r_associated | relid=0 | w=32
  143. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:menkes disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:menkes disease | rel=r_associated | relid=0 | w=32
  144. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:mental retardation, x-linked, snyder-robinson type
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:mental retardation, x-linked, snyder-robinson type | rel=r_associated | relid=0 | w=32
  145. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:multiple acyl-coa dehydrogenase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:multiple acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=32
  146. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:multiple carboxylase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:multiple carboxylase deficiency | rel=r_associated | relid=0 | w=32
  147. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:muscle l-lactate dehydrogenase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:muscle l-lactate dehydrogenase deficiency | rel=r_associated | relid=0 | w=32
  148. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:newborn conditions with positive markers:prid:pt:bld.dot:nom
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:newborn conditions with positive markers:prid:pt:bld.dot:nom | rel=r_associated | relid=0 | w=32
  149. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:nursing therapy
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:nursing therapy | rel=r_associated | relid=0 | w=32
  150. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:orofaciodigital syndromes
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=32
  151. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:otc, ivs4, a-t, -2
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, ivs4, a-t, -2 | rel=r_associated | relid=0 | w=32
  152. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:pathological aspects
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:pathological aspects | rel=r_associated | relid=0 | w=32
  153. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:pediatric failure to thrive
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:pediatric failure to thrive | rel=r_associated | relid=0 | w=32
  154. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:phenylketonuria ii
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:phenylketonuria ii | rel=r_associated | relid=0 | w=32
  155. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:pseudohypoparathyroidism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:pseudohypoparathyroidism | rel=r_associated | relid=0 | w=32
  156. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:pyridoxine dependency syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:pyridoxine dependency syndrome | rel=r_associated | relid=0 | w=32
  157. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:pyruvate carboxylase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=32
  158. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:transient hyperammonemia in infancy
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:transient hyperammonemia in infancy | rel=r_associated | relid=0 | w=32
  159. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 32 / 0.744 -> en:unclassified metabolic disorder
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:unclassified metabolic disorder | rel=r_associated | relid=0 | w=32
  160. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> déficit en ornithine carbamyltransférase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=déficit en ornithine carbamyltransférase | rel=r_associated | relid=0 | w=31
  161. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:acquired lactase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:acquired lactase deficiency | rel=r_associated | relid=0 | w=31
  162. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:amino acid deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:amino acid deficiency | rel=r_associated | relid=0 | w=31
  163. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:aminomethyltransferase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:aminomethyltransferase deficiency | rel=r_associated | relid=0 | w=31
  164. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:angiokeratoma corporis diffusum
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:angiokeratoma corporis diffusum | rel=r_associated | relid=0 | w=31
  165. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:beta-aminoisobutyricaciduria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:beta-aminoisobutyricaciduria | rel=r_associated | relid=0 | w=31
  166. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:congenital nephrogenic diabetes insipidus
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:congenital nephrogenic diabetes insipidus | rel=r_associated | relid=0 | w=31
  167. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:crigler-najjar syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:crigler-najjar syndrome | rel=r_associated | relid=0 | w=31
  168. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:dent's disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:dent's disease | rel=r_associated | relid=0 | w=31
  169. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:developmental delay
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:developmental delay | rel=r_associated | relid=0 | w=31
  170. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:disorder of pyruvate metabolism and mitochondrial respiratory chain
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:disorder of pyruvate metabolism and mitochondrial respiratory chain | rel=r_associated | relid=0 | w=31
  171. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:enterokinase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=31
  172. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:episodic ammonia intoxication
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:episodic ammonia intoxication | rel=r_associated | relid=0 | w=31
  173. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:familial amyloidosis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:familial amyloidosis | rel=r_associated | relid=0 | w=31
  174. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:female restricted epilepsy with intellectual disability syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:female restricted epilepsy with intellectual disability syndrome | rel=r_associated | relid=0 | w=31
  175. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:focal dermal hypoplasia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:focal dermal hypoplasia | rel=r_associated | relid=0 | w=31
  176. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:folinic acid responsive seizure syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:folinic acid responsive seizure syndrome | rel=r_associated | relid=0 | w=31
  177. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:glycogen storage disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glycogen storage disease | rel=r_associated | relid=0 | w=31
  178. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:glycogen storage disease type vi
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glycogen storage disease type vi | rel=r_associated | relid=0 | w=31
  179. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:hereditary hyperbilirubinemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hereditary hyperbilirubinemia | rel=r_associated | relid=0 | w=31
  180. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:homocystinemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:homocystinemia | rel=r_associated | relid=0 | w=31
  181. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:hyperlipoproteinemia type i
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperlipoproteinemia type i | rel=r_associated | relid=0 | w=31
  182. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:inborn biological transport disorder
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:inborn biological transport disorder | rel=r_associated | relid=0 | w=31
  183. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:inborn error of lipoprotein metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=31
  184. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:inborn errors of carbohydrate metabolism (excl glucose)
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:inborn errors of carbohydrate metabolism (excl glucose) | rel=r_associated | relid=0 | w=31
  185. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:inborn errors of porphyrin metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:inborn errors of porphyrin metabolism | rel=r_associated | relid=0 | w=31
  186. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:lissencephaly, x-linked, 2
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:lissencephaly, x-linked, 2 | rel=r_associated | relid=0 | w=31
  187. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:mental retardation, x-linked, syndromic, christianson type
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:mental retardation, x-linked, syndromic, christianson type | rel=r_associated | relid=0 | w=31
  188. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:moderate steroid 21-hydroxylase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:moderate steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=31
  189. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:moloney syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:moloney syndrome | rel=r_associated | relid=0 | w=31
  190. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:nance-horan syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:nance-horan syndrome | rel=r_associated | relid=0 | w=31
  191. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:neuronal ceroid lipofuscinosis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:neuronal ceroid lipofuscinosis | rel=r_associated | relid=0 | w=31
  192. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:otc, arg129his
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, arg129his | rel=r_associated | relid=0 | w=31
  193. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:otc, del
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, del | rel=r_associated | relid=0 | w=31
  194. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:otc, gt-gc, intron 7
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, gt-gc, intron 7 | rel=r_associated | relid=0 | w=31
  195. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:phosphoglycerate kinase 1 deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:phosphoglycerate kinase 1 deficiency | rel=r_associated | relid=0 | w=31
  196. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:placental steroid sulfatase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:placental steroid sulfatase deficiency | rel=r_associated | relid=0 | w=31
  197. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:prevalence of 1 in 40,000 to 1 in 80,000
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:prevalence of 1 in 40,000 to 1 in 80,000 | rel=r_associated | relid=0 | w=31
  198. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:propionic acidemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:propionic acidemia | rel=r_associated | relid=0 | w=31
  199. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:renpenning syndrome 1
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:renpenning syndrome 1 | rel=r_associated | relid=0 | w=31
  200. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:respiratory alkalosis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:respiratory alkalosis | rel=r_associated | relid=0 | w=31
  201. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:taxonomic
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:taxonomic | rel=r_associated | relid=0 | w=31
  202. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:thyroid dyshormonogenesis 4
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:thyroid dyshormonogenesis 4 | rel=r_associated | relid=0 | w=31
  203. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:viruses
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:viruses | rel=r_associated | relid=0 | w=31
  204. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:vomiting
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:vomiting | rel=r_associated | relid=0 | w=31
  205. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:x-linked dystonia parkinsonism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked dystonia parkinsonism | rel=r_associated | relid=0 | w=31
  206. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> en:x-linked ichthyosis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked ichthyosis | rel=r_associated | relid=0 | w=31
  207. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 31 / 0.721 -> hyperammoniémie de type ii
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=hyperammoniémie de type ii | rel=r_associated | relid=0 | w=31
  208. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> déficit en ornithine-transcarbamylase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=déficit en ornithine-transcarbamylase | rel=r_associated | relid=0 | w=30
  209. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:17-beta-hydroxysteroid dehydrogenase 3 deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:17-beta-hydroxysteroid dehydrogenase 3 deficiency | rel=r_associated | relid=0 | w=30
  210. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:5-oxoprolinase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:5-oxoprolinase deficiency | rel=r_associated | relid=0 | w=30
  211. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:aldosterone synthase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:aldosterone synthase deficiency | rel=r_associated | relid=0 | w=30
  212. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:amino acid/carbohydrate metabolic disorder
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:amino acid/carbohydrate metabolic disorder | rel=r_associated | relid=0 | w=30
  213. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:carrier females may present with postpartum hyperammonemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:carrier females may present with postpartum hyperammonemia | rel=r_associated | relid=0 | w=30
  214. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:cask related intellectual disability
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:cask related intellectual disability | rel=r_associated | relid=0 | w=30
  215. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:craniofrontonasal dysplasia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:craniofrontonasal dysplasia | rel=r_associated | relid=0 | w=30
  216. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:cystinuria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:cystinuria | rel=r_associated | relid=0 | w=30
  217. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:disorder due to n-acetyltransferase enzyme variant
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:disorder due to n-acetyltransferase enzyme variant | rel=r_associated | relid=0 | w=30
  218. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:disorder of glycoprotein metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:disorder of glycoprotein metabolism | rel=r_associated | relid=0 | w=30
  219. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:disorder of lysine and hydroxylysine metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:disorder of lysine and hydroxylysine metabolism | rel=r_associated | relid=0 | w=30
  220. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:disorder of sulfur-bearing amino acid metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:disorder of sulfur-bearing amino acid metabolism | rel=r_associated | relid=0 | w=30
  221. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:dyskeratosis congenita
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:dyskeratosis congenita | rel=r_associated | relid=0 | w=30
  222. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:ehlers-danlos syndrome, arthrochalasia type
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ehlers-danlos syndrome, arthrochalasia type | rel=r_associated | relid=0 | w=30
  223. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:emery-dreifuss muscular dystrophy
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:emery-dreifuss muscular dystrophy | rel=r_associated | relid=0 | w=30
  224. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:exposure as collected domain
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:exposure as collected domain | rel=r_associated | relid=0 | w=30
  225. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:fatty acid metabolism disorder
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:fatty acid metabolism disorder | rel=r_associated | relid=0 | w=30
  226. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:fraxe intellectual disability syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:fraxe intellectual disability syndrome | rel=r_associated | relid=0 | w=30
  227. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:genetic aspects
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:genetic aspects | rel=r_associated | relid=0 | w=30
  228. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:glycine dehydrogenase (decarboxylating) deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glycine dehydrogenase (decarboxylating) deficiency | rel=r_associated | relid=0 | w=30
  229. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:high ornithine
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:high ornithine | rel=r_associated | relid=0 | w=30
  230. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:hydroxykynureninuria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hydroxykynureninuria | rel=r_associated | relid=0 | w=30
  231. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:hyperandrogenism due to non-classic 21-hydroxylase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperandrogenism due to non-classic 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=30
  232. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:hyperornithinemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperornithinemia | rel=r_associated | relid=0 | w=30
  233. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:inborn error of glutathione metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:inborn error of glutathione metabolism | rel=r_associated | relid=0 | w=30
  234. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:irritation
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:irritation | rel=r_associated | relid=0 | w=30
  235. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:lactase deficiency, congenital
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:lactase deficiency, congenital | rel=r_associated | relid=0 | w=30
  236. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:metal metabolism, inborn errors
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:metal metabolism, inborn errors | rel=r_associated | relid=0 | w=30
  237. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:microphthalmia, syndromic 2
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:microphthalmia, syndromic 2 | rel=r_associated | relid=0 | w=30
  238. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:microphthalmia, syndromic 4 (disorder)
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:microphthalmia, syndromic 4 (disorder) | rel=r_associated | relid=0 | w=30
  239. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:muscle amp deaminase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:muscle amp deaminase deficiency | rel=r_associated | relid=0 | w=30
  240. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:opitz g/bbb syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:opitz g/bbb syndrome | rel=r_associated | relid=0 | w=30
  241. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:organic acid metabolism disorder
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:organic acid metabolism disorder | rel=r_associated | relid=0 | w=30
  242. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:ornithine carbamoyl phosphate deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ornithine carbamoyl phosphate deficiency | rel=r_associated | relid=0 | w=30
  243. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:ornithine carbamoyltransferase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ornithine carbamoyltransferase deficiency | rel=r_associated | relid=0 | w=30
  244. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:otc, arg109gln
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, arg109gln | rel=r_associated | relid=0 | w=30
  245. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:otc, gln216glu
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, gln216glu | rel=r_associated | relid=0 | w=30
  246. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:otc, glu87lys
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, glu87lys | rel=r_associated | relid=0 | w=30
  247. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:otc, gta-gtg, intron 7
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, gta-gtg, intron 7 | rel=r_associated | relid=0 | w=30
  248. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:otc, leu111pro
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, leu111pro | rel=r_associated | relid=0 | w=30
  249. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:otc, met206arg
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, met206arg | rel=r_associated | relid=0 | w=30
  250. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:pancreatic trypsinogen deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:pancreatic trypsinogen deficiency | rel=r_associated | relid=0 | w=30
  251. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:pharmacotherapeutic
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:pharmacotherapeutic | rel=r_associated | relid=0 | w=30
  252. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:renal aminoacidurias
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:renal aminoacidurias | rel=r_associated | relid=0 | w=30
  253. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:renal tubular transport, inborn errors
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:renal tubular transport, inborn errors | rel=r_associated | relid=0 | w=30
  254. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:rett syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:rett syndrome | rel=r_associated | relid=0 | w=30
  255. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:sex chromosome disorders of sex development
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:sex chromosome disorders of sex development | rel=r_associated | relid=0 | w=30
  256. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:steroid metabolism, inborn errors
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:steroid metabolism, inborn errors | rel=r_associated | relid=0 | w=30
  257. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:surgical aspects
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:surgical aspects | rel=r_associated | relid=0 | w=30
  258. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:urea cycle metabolism disorder
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:urea cycle metabolism disorder | rel=r_associated | relid=0 | w=30
  259. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 30 / 0.698 -> en:x-linked retinal dysplasia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked retinal dysplasia | rel=r_associated | relid=0 | w=30
  260. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> déficit en ornithinecarbamyl-transférase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=déficit en ornithinecarbamyl-transférase | rel=r_associated | relid=0 | w=29
  261. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:albinism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:albinism | rel=r_associated | relid=0 | w=29
  262. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:alpha-1 antitrypsin deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=29
  263. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:amino acid transport disorder
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:amino acid transport disorder | rel=r_associated | relid=0 | w=29
  264. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:aspects of mortality statistics
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:aspects of mortality statistics | rel=r_associated | relid=0 | w=29
  265. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:asymptomatic hyperammonemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:asymptomatic hyperammonemia | rel=r_associated | relid=0 | w=29
  266. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:barth syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:barth syndrome | rel=r_associated | relid=0 | w=29
  267. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:beta thalassemia x-linked thrombocytopenia syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:beta thalassemia x-linked thrombocytopenia syndrome | rel=r_associated | relid=0 | w=29
  268. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:choroideremia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:choroideremia | rel=r_associated | relid=0 | w=29
  269. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:classical phenylketonuria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  270. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:congenital sucrase-isomaltase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=29
  271. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:cystinosis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:cystinosis | rel=r_associated | relid=0 | w=29
  272. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:deficiency in enzyme complexes of mitochondrial respiratory chain
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:deficiency in enzyme complexes of mitochondrial respiratory chain | rel=r_associated | relid=0 | w=29
  273. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:disorder of ornithine metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:disorder of ornithine metabolism | rel=r_associated | relid=0 | w=29
  274. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:embryologic
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:embryologic | rel=r_associated | relid=0 | w=29
  275. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:fanconi syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:fanconi syndrome | rel=r_associated | relid=0 | w=29
  276. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:glycogen storage disease type viii
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glycogen storage disease type viii | rel=r_associated | relid=0 | w=29
  277. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:hereditary methemoglobinemia, enzymatic type
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hereditary methemoglobinemia, enzymatic type | rel=r_associated | relid=0 | w=29
  278. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:hmg-coa lyase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=29
  279. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:hnsha due to nadh diaphorase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hnsha due to nadh diaphorase deficiency | rel=r_associated | relid=0 | w=29
  280. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:holoprosencephaly with fetal akinesia-hypokinesia sequence
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | rel=r_associated | relid=0 | w=29
  281. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:homocystinuria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:homocystinuria | rel=r_associated | relid=0 | w=29
  282. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:hyper-igm immunodeficiency syndrome, type 1
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyper-igm immunodeficiency syndrome, type 1 | rel=r_associated | relid=0 | w=29
  283. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:hyperlysinemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperlysinemia | rel=r_associated | relid=0 | w=29
  284. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:hypophosphatasia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hypophosphatasia | rel=r_associated | relid=0 | w=29
  285. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:inborn lipid/lipoprotein disorder
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:inborn lipid/lipoprotein disorder | rel=r_associated | relid=0 | w=29
  286. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:inherited disorder of thyroid metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:inherited disorder of thyroid metabolism | rel=r_associated | relid=0 | w=29
  287. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:intermediary metabolism disorder
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:intermediary metabolism disorder | rel=r_associated | relid=0 | w=29
  288. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:lysinuric protein intolerance
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:lysinuric protein intolerance | rel=r_associated | relid=0 | w=29
  289. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:methylenetetrahydrofolate reductase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:methylenetetrahydrofolate reductase deficiency | rel=r_associated | relid=0 | w=29
  290. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:mohr-tranebjaerg syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:mohr-tranebjaerg syndrome | rel=r_associated | relid=0 | w=29
  291. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:neonatal research network terminology
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:neonatal research network terminology | rel=r_associated | relid=0 | w=29
  292. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:oculocerebrorenal syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=29
  293. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:otc, arg40his
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, arg40his | rel=r_associated | relid=0 | w=29
  294. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:otc, arg62thr
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, arg62thr | rel=r_associated | relid=0 | w=29
  295. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:otc, glu154ter
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, glu154ter | rel=r_associated | relid=0 | w=29
  296. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:otc, gly50ter
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, gly50ter | rel=r_associated | relid=0 | w=29
  297. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:otc, pro225leu
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, pro225leu | rel=r_associated | relid=0 | w=29
  298. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:other specified disorders of amino-acid transport and metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:other specified disorders of amino-acid transport and metabolism | rel=r_associated | relid=0 | w=29
  299. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:periventricular heterotopia, x-linked
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:periventricular heterotopia, x-linked | rel=r_associated | relid=0 | w=29
  300. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:physiopathological
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:physiopathological | rel=r_associated | relid=0 | w=29
  301. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:premature aging syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:premature aging syndrome | rel=r_associated | relid=0 | w=29
  302. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:progeria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:progeria | rel=r_associated | relid=0 | w=29
  303. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:roentgenographic
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:roentgenographic | rel=r_associated | relid=0 | w=29
  304. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:sarcosinemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:sarcosinemia | rel=r_associated | relid=0 | w=29
  305. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:some carrier females have episodes of significant hyperammonemia in infancy or childhood
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:some carrier females have episodes of significant hyperammonemia in infancy or childhood | rel=r_associated | relid=0 | w=29
  306. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:stroke (rare)
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:stroke (rare) | rel=r_associated | relid=0 | w=29
  307. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:waisman syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:waisman syndrome | rel=r_associated | relid=0 | w=29
  308. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 29 / 0.674 -> en:wiskott-aldrich syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:wiskott-aldrich syndrome | rel=r_associated | relid=0 | w=29
  309. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:arakawa syndrome ii
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:arakawa syndrome ii | rel=r_associated | relid=0 | w=28
  310. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:benign neonatal hyperaminoaciduria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:benign neonatal hyperaminoaciduria | rel=r_associated | relid=0 | w=28
  311. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:beta-methylcrotonylglycinuria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:beta-methylcrotonylglycinuria | rel=r_associated | relid=0 | w=28
  312. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:diagnosis aspect
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:diagnosis aspect | rel=r_associated | relid=0 | w=28
  313. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:dihydrouracil dehydrogenase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:dihydrouracil dehydrogenase deficiency | rel=r_associated | relid=0 | w=28
  314. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:etiology aspects
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:etiology aspects | rel=r_associated | relid=0 | w=28
  315. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:ferrochelatase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ferrochelatase deficiency | rel=r_associated | relid=0 | w=28
  316. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:hemophilia a
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hemophilia a | rel=r_associated | relid=0 | w=28
  317. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:high plasma asparagine
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:high plasma asparagine | rel=r_associated | relid=0 | w=28
  318. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:hypermethioniuria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hypermethioniuria | rel=r_associated | relid=0 | w=28
  319. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:hyperphenylalaninemia, non phenylketonuric
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperphenylalaninemia, non phenylketonuric | rel=r_associated | relid=0 | w=28
  320. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:hyperprolinemia type 1
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperprolinemia type 1 | rel=r_associated | relid=0 | w=28
  321. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:in cerebrospinal fluid
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:in cerebrospinal fluid | rel=r_associated | relid=0 | w=28
  322. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:lubs x-linked mental retardation syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:lubs x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=28
  323. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:mental retardation, x-linked
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:mental retardation, x-linked | rel=r_associated | relid=0 | w=28
  324. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:molybdenum cofactor deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:molybdenum cofactor deficiency | rel=r_associated | relid=0 | w=28
  325. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:myoglobinuria, recurrent
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:myoglobinuria, recurrent | rel=r_associated | relid=0 | w=28
  326. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:newborn conditions with equivocal markers:prid:pt:bld.dot:nom
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:newborn conditions with equivocal markers:prid:pt:bld.dot:nom | rel=r_associated | relid=0 | w=28
  327. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:nutritional management
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:nutritional management | rel=r_associated | relid=0 | w=28
  328. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:ornithine carbamoyltransferase:ccnc:pt:amnio fld:qn
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ornithine carbamoyltransferase:ccnc:pt:amnio fld:qn | rel=r_associated | relid=0 | w=28
  329. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:otc, arg277trp
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, arg277trp | rel=r_associated | relid=0 | w=28
  330. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:otc, gly162arg
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, gly162arg | rel=r_associated | relid=0 | w=28
  331. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:pediatric terminology
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:pediatric terminology | rel=r_associated | relid=0 | w=28
  332. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:peroxisomal disorder
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:peroxisomal disorder | rel=r_associated | relid=0 | w=28
  333. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:purine-nucleoside phosphorylase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:purine-nucleoside phosphorylase deficiency | rel=r_associated | relid=0 | w=28
  334. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:transitory amino acid metabolic disorder
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:transitory amino acid metabolic disorder | rel=r_associated | relid=0 | w=28
  335. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:tyrosinemia, type iii
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:tyrosinemia, type iii | rel=r_associated | relid=0 | w=28
  336. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:x-linked agammaglobulinemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked agammaglobulinemia | rel=r_associated | relid=0 | w=28
  337. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 28 / 0.651 -> en:x-linked bulbar-muscular atrophy
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked bulbar-muscular atrophy | rel=r_associated | relid=0 | w=28
  338. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> carence en ornithine transcarbamylase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=carence en ornithine transcarbamylase | rel=r_associated | relid=0 | w=27
  339. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:acetyl-coa: carboxylase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:acetyl-coa: carboxylase deficiency | rel=r_associated | relid=0 | w=27
  340. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:acute hyperammonemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:acute hyperammonemia | rel=r_associated | relid=0 | w=27
  341. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:adult hypophosphatasia (disorder)
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:adult hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  342. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:alpha, alpha-trehalase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:alpha, alpha-trehalase deficiency | rel=r_associated | relid=0 | w=27
  343. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:aminoaciduria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:aminoaciduria | rel=r_associated | relid=0 | w=27
  344. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:butyryl-coa dehydrogenase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:butyryl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=27
  345. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:chemically induced
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:chemically induced | rel=r_associated | relid=0 | w=27
  346. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:complication aspects
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:complication aspects | rel=r_associated | relid=0 | w=27
  347. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:dermoids of cornea
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:dermoids of cornea | rel=r_associated | relid=0 | w=27
  348. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:dihydropyrimidine dehydrogenase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:dihydropyrimidine dehydrogenase deficiency | rel=r_associated | relid=0 | w=27
  349. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:duchenne muscular dystrophy
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:duchenne muscular dystrophy | rel=r_associated | relid=0 | w=27
  350. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:familial renal iminoglycinuria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:familial renal iminoglycinuria | rel=r_associated | relid=0 | w=27
  351. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:genetic diseases, x-linked
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  352. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:glucose-6-phosphate dehydrogenase deficiency anemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glucose-6-phosphate dehydrogenase deficiency anemia | rel=r_associated | relid=0 | w=27
  353. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:glutathione s-transferase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glutathione s-transferase deficiency | rel=r_associated | relid=0 | w=27
  354. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:glycine encephalopathy
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glycine encephalopathy | rel=r_associated | relid=0 | w=27
  355. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:glycogen storage disease type iib
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glycogen storage disease type iib | rel=r_associated | relid=0 | w=27
  356. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:hydroxyprolinemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hydroxyprolinemia | rel=r_associated | relid=0 | w=27
  357. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:hyperammonemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperammonemia | rel=r_associated | relid=0 | w=27
  358. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:hyperhomocysteinemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperhomocysteinemia | rel=r_associated | relid=0 | w=27
  359. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:increased aromatase activity
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:increased aromatase activity | rel=r_associated | relid=0 | w=27
  360. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:intestinal disaccharidase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:intestinal disaccharidase deficiency | rel=r_associated | relid=0 | w=27
  361. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:lysosomal storage disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:lysosomal storage disease | rel=r_associated | relid=0 | w=27
  362. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:methylenetetrahydrofolate reductase gene mutation
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:methylenetetrahydrofolate reductase gene mutation | rel=r_associated | relid=0 | w=27
  363. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:microcephaly microcornea syndrome seemanova type
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:microcephaly microcornea syndrome seemanova type | rel=r_associated | relid=0 | w=27
  364. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:ocular albinism, type ii
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ocular albinism, type ii | rel=r_associated | relid=0 | w=27
  365. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:ornithine carbamoyltransferase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ornithine carbamoyltransferase | rel=r_associated | relid=0 | w=27
  366. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:ornithine carbamoyltransferase:ccnc:pt:ser:qn
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ornithine carbamoyltransferase:ccnc:pt:ser:qn | rel=r_associated | relid=0 | w=27
  367. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:otc, arg109ter
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, arg109ter | rel=r_associated | relid=0 | w=27
  368. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:otc, arg26gln
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, arg26gln | rel=r_associated | relid=0 | w=27
  369. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:otc, gly47glu
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, gly47glu | rel=r_associated | relid=0 | w=27
  370. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:otc, leu272phe
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, leu272phe | rel=r_associated | relid=0 | w=27
  371. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:otc, leu45pro
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, leu45pro | rel=r_associated | relid=0 | w=27
  372. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:other disorders of aromatic amino-acid metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:other disorders of aromatic amino-acid metabolism | rel=r_associated | relid=0 | w=27
  373. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:other disorders of urea cycle metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:other disorders of urea cycle metabolism | rel=r_associated | relid=0 | w=27
  374. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:other disturbances of straight-chain amino-acid metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:other disturbances of straight-chain amino-acid metabolism | rel=r_associated | relid=0 | w=27
  375. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:pancreatic colipase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:pancreatic colipase deficiency | rel=r_associated | relid=0 | w=27
  376. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:prolidase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=27
  377. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:severe steroid 21-hydroxylase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:severe steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=27
  378. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:sulfite oxidase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:sulfite oxidase deficiency | rel=r_associated | relid=0 | w=27
  379. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:ugt1a1*28 polymorphism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ugt1a1*28 polymorphism | rel=r_associated | relid=0 | w=27
  380. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:use of ultrasonography
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:use of ultrasonography | rel=r_associated | relid=0 | w=27
  381. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:valinemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:valinemia | rel=r_associated | relid=0 | w=27
  382. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:veterinary aspects
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:veterinary aspects | rel=r_associated | relid=0 | w=27
  383. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:vrozené poruchy metabolismu nec in mdrcze18_1
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:vrozené poruchy metabolismu nec in mdrcze18_1 | rel=r_associated | relid=0 | w=27
  384. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:wolman disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:wolman disease | rel=r_associated | relid=0 | w=27
  385. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> en:x-linked lymphoproliferative syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked lymphoproliferative syndrome | rel=r_associated | relid=0 | w=27
  386. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 27 / 0.628 -> maladie
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=maladie | rel=r_associated | relid=0 | w=27
  387. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:aicardi syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=26
  388. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:alpha thalassemia x-linked mental retardation syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:alpha thalassemia x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=26
  389. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:carbohydrate metabolism, inborn errors
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:carbohydrate metabolism, inborn errors | rel=r_associated | relid=0 | w=26
  390. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:cerebral edema
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:cerebral edema | rel=r_associated | relid=0 | w=26
  391. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:chronic granulomatous disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:chronic granulomatous disease | rel=r_associated | relid=0 | w=26
  392. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:congenital adrenal hyperplasia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=26
  393. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:cystathionine beta-synthase deficiency disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:cystathionine beta-synthase deficiency disease | rel=r_associated | relid=0 | w=26
  394. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:disorder due to cytochrome p450 enzyme variant
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:disorder due to cytochrome p450 enzyme variant | rel=r_associated | relid=0 | w=26
  395. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:disorder of sialic acid metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:disorder of sialic acid metabolism | rel=r_associated | relid=0 | w=26
  396. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency | rel=r_associated | relid=0 | w=26
  397. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:galactosemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:galactosemia | rel=r_associated | relid=0 | w=26
  398. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:glutamate-cysteine ligase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glutamate-cysteine ligase deficiency | rel=r_associated | relid=0 | w=26
  399. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:hartnup disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hartnup disease | rel=r_associated | relid=0 | w=26
  400. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:hereditary orotic aciduria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hereditary orotic aciduria | rel=r_associated | relid=0 | w=26
  401. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:historical aspects qualifier
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:historical aspects qualifier | rel=r_associated | relid=0 | w=26
  402. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:hnsha due to hexokinase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hnsha due to hexokinase deficiency | rel=r_associated | relid=0 | w=26
  403. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:homocarnosinosis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:homocarnosinosis | rel=r_associated | relid=0 | w=26
  404. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:hyperinsulinemic hypoglycemia, familial, 6
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperinsulinemic hypoglycemia, familial, 6 | rel=r_associated | relid=0 | w=26
  405. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:immunology aspects
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:immunology aspects | rel=r_associated | relid=0 | w=26
  406. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:inborn errors of bilirubin metabolism
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:inborn errors of bilirubin metabolism | rel=r_associated | relid=0 | w=26
  407. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:inborn immunodeficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:inborn immunodeficiency | rel=r_associated | relid=0 | w=26
  408. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:infantile hypophosphatasia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:infantile hypophosphatasia | rel=r_associated | relid=0 | w=26
  409. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:inherited metabolic disorder of nervous system
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:inherited metabolic disorder of nervous system | rel=r_associated | relid=0 | w=26
  410. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:juvenile x-linked retinoschisis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:juvenile x-linked retinoschisis | rel=r_associated | relid=0 | w=26
  411. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:masa syndrome (disorder)
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:masa syndrome (disorder) | rel=r_associated | relid=0 | w=26
  412. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:methionine adenosyltransferase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:methionine adenosyltransferase deficiency | rel=r_associated | relid=0 | w=26
  413. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:methylmalonic aciduria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:methylmalonic aciduria | rel=r_associated | relid=0 | w=26
  414. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:muscle d-lactate dehydrogenase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:muscle d-lactate dehydrogenase deficiency | rel=r_associated | relid=0 | w=26
  415. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:ocular albinism type 1
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ocular albinism type 1 | rel=r_associated | relid=0 | w=26
  416. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:otc, arg40cys
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:otc, arg40cys | rel=r_associated | relid=0 | w=26
  417. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:pancreatic alpha-amylase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:pancreatic alpha-amylase deficiency | rel=r_associated | relid=0 | w=26
  418. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:parasitology
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:parasitology | rel=r_associated | relid=0 | w=26
  419. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:purine-pyrimidine metabolism, inborn errors
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:purine-pyrimidine metabolism, inborn errors | rel=r_associated | relid=0 | w=26
  420. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:pyruvate kinase deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:pyruvate kinase deficiency | rel=r_associated | relid=0 | w=26
  421. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:specific enzyme deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:specific enzyme deficiency | rel=r_associated | relid=0 | w=26
  422. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:storage disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:storage disease | rel=r_associated | relid=0 | w=26
  423. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:two types - lethal neonatal and less severe, late onset
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:two types - lethal neonatal and less severe, late onset | rel=r_associated | relid=0 | w=26
  424. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:tyrosinemia type ii
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:tyrosinemia type ii | rel=r_associated | relid=0 | w=26
  425. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:x chromosome-linked pyridoxine refractory sideroblastic anemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x chromosome-linked pyridoxine refractory sideroblastic anemia | rel=r_associated | relid=0 | w=26
  426. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:x-linked adrenal hypoplasia congenita
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked adrenal hypoplasia congenita | rel=r_associated | relid=0 | w=26
  427. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 26 / 0.605 -> en:x-linked dyskeratosis congenita
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:x-linked dyskeratosis congenita | rel=r_associated | relid=0 | w=26
  428. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 25 / 0.581 -> en:ornithine
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:ornithine | rel=r_associated | relid=0 | w=25
  429. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 25 / 0.581 -> transférase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=transférase | rel=r_associated | relid=0 | w=25
  430. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 24 / 0.558 -> vomissement
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=vomissement | rel=r_associated | relid=0 | w=24
  431. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> absence de croissance
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=absence de croissance | rel=r_associated | relid=0 | w=20
  432. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> acidémie glutarique de type 1
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=acidémie glutarique de type 1 | rel=r_associated | relid=0 | w=20
  433. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> acidurie glutarique de type 1
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=acidurie glutarique de type 1 | rel=r_associated | relid=0 | w=20
  434. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> albinisme
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=albinisme | rel=r_associated | relid=0 | w=20
  435. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> arriération
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=arriération | rel=r_associated | relid=0 | w=20
  436. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> arriération mentale
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=arriération mentale | rel=r_associated | relid=0 | w=20
  437. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> asthénie sénile
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=asthénie sénile | rel=r_associated | relid=0 | w=20
  438. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> cétoacidurie à chaînes ramifiées
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=cétoacidurie à chaînes ramifiées | rel=r_associated | relid=0 | w=20
  439. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> congénital
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=congénital | rel=r_associated | relid=0 | w=20
  440. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> congenital
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=congenital | rel=r_associated | relid=0 | w=20
  441. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> congénitale
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=congénitale | rel=r_associated | relid=0 | w=20
  442. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> contractures congénitales et arachnodactylie
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=contractures congénitales et arachnodactylie | rel=r_associated | relid=0 | w=20
  443. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> débilité mentale
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=débilité mentale | rel=r_associated | relid=0 | w=20
  444. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> débilité sénile
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=débilité sénile | rel=r_associated | relid=0 | w=20
  445. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> déficience intellectuelle
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=déficience intellectuelle | rel=r_associated | relid=0 | w=20
  446. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> déficience mentale
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=déficience mentale | rel=r_associated | relid=0 | w=20
  447. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> déficit en céto-acide décarboxylase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=déficit en céto-acide décarboxylase | rel=r_associated | relid=0 | w=20
  448. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> déficit en cytochrome oxydase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=déficit en cytochrome oxydase | rel=r_associated | relid=0 | w=20
  449. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> déficit en cytochrome-c oxydase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=déficit en cytochrome-c oxydase | rel=r_associated | relid=0 | w=20
  450. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> déficit en prolidase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=déficit en prolidase | rel=r_associated | relid=0 | w=20
  451. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> déficit en pyruvate carboxylase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=déficit en pyruvate carboxylase | rel=r_associated | relid=0 | w=20
  452. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> déficit en semialdéhyde succinique-déshydrogénase
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=déficit en semialdéhyde succinique-déshydrogénase | rel=r_associated | relid=0 | w=20
  453. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> déliquescence
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=déliquescence | rel=r_associated | relid=0 | w=20
  454. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> démence (sémiologie)
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=démence (sémiologie) | rel=r_associated | relid=0 | w=20
  455. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> démence dégénérative primaire
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=démence dégénérative primaire | rel=r_associated | relid=0 | w=20
  456. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> démence forme dépressive ou délirante
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=démence forme dépressive ou délirante | rel=r_associated | relid=0 | w=20
  457. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> démence présénile
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=démence présénile | rel=r_associated | relid=0 | w=20
  458. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> démence sénile
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=démence sénile | rel=r_associated | relid=0 | w=20
  459. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> démence sénile avec delirium ou état confusionnel aigu
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=démence sénile avec delirium ou état confusionnel aigu | rel=r_associated | relid=0 | w=20
  460. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> dyslipémie
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=dyslipémie | rel=r_associated | relid=0 | w=20
  461. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> dystrophie musculaire d'Emery-Dreifuss
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=dystrophie musculaire d'Emery-Dreifuss | rel=r_associated | relid=0 | w=20
  462. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> dystrophie musculaire d'emery-dreifuss
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=dystrophie musculaire d'emery-dreifuss | rel=r_associated | relid=0 | w=20
  463. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:age-related physical debility
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:age-related physical debility | rel=r_associated | relid=0 | w=20
  464. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:branched-chain ketoaciduria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:branched-chain ketoaciduria | rel=r_associated | relid=0 | w=20
  465. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:classical maple syrup urine disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:classical maple syrup urine disease | rel=r_associated | relid=0 | w=20
  466. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:emesia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:emesia | rel=r_associated | relid=0 | w=20
  467. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:emesis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:emesis | rel=r_associated | relid=0 | w=20
  468. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:epidemiological
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:epidemiological | rel=r_associated | relid=0 | w=20
  469. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:fragile X syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:fragile X syndrome | rel=r_associated | relid=0 | w=20
  470. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:Gaucher disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:Gaucher disease | rel=r_associated | relid=0 | w=20
  471. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:glutaric aciduria, type 1
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:glutaric aciduria, type 1 | rel=r_associated | relid=0 | w=20
  472. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:Goltz syndrome
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:Goltz syndrome | rel=r_associated | relid=0 | w=20
  473. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:hemophilia A
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hemophilia A | rel=r_associated | relid=0 | w=20
  474. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:hemophilia B
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hemophilia B | rel=r_associated | relid=0 | w=20
  475. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:histidinaemia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:histidinaemia | rel=r_associated | relid=0 | w=20
  476. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:hyperlipoproteinemia type I
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hyperlipoproteinemia type I | rel=r_associated | relid=0 | w=20
  477. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:hypophosphatasia infantile
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:hypophosphatasia infantile | rel=r_associated | relid=0 | w=20
  478. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:learning disability
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:learning disability | rel=r_associated | relid=0 | w=20
  479. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:leucinosis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  480. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:maple-tree syrup disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:maple-tree syrup disease | rel=r_associated | relid=0 | w=20
  481. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:mental deficiency
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:mental deficiency | rel=r_associated | relid=0 | w=20
  482. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:mental handicap
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:mental handicap | rel=r_associated | relid=0 | w=20
  483. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:morosis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:morosis | rel=r_associated | relid=0 | w=20
  484. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:muscular dystrophy, emery-dreifuss
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:muscular dystrophy, emery-dreifuss | rel=r_associated | relid=0 | w=20
  485. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:nystagmus
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:nystagmus | rel=r_associated | relid=0 | w=20
  486. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:oligergasia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:oligergasia | rel=r_associated | relid=0 | w=20
  487. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:oligopsychia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:oligopsychia | rel=r_associated | relid=0 | w=20
  488. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:oxalosis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:oxalosis | rel=r_associated | relid=0 | w=20
  489. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:phenylpyruvic oligophrenia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:phenylpyruvic oligophrenia | rel=r_associated | relid=0 | w=20
  490. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:presenile dementia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:presenile dementia | rel=r_associated | relid=0 | w=20
  491. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:retardation
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
  492. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:senile asthenia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:senile asthenia | rel=r_associated | relid=0 | w=20
  493. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:senile dementia
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:senile dementia | rel=r_associated | relid=0 | w=20
  494. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:senility
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:senility | rel=r_associated | relid=0 | w=20
  495. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:thiamin-responsive maple syrup urine disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:thiamin-responsive maple syrup urine disease | rel=r_associated | relid=0 | w=20
  496. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:type I
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:type I | rel=r_associated | relid=0 | w=20
  497. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:tyrosinemia type II
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:tyrosinemia type II | rel=r_associated | relid=0 | w=20
  498. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:unspecified senile psychotic condition
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:unspecified senile psychotic condition | rel=r_associated | relid=0 | w=20
  499. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:Wolman's disease
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:Wolman's disease | rel=r_associated | relid=0 | w=20
  500. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> en:X-linked
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:X-linked | rel=r_associated | relid=0 | w=20
  501. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> enzymologie
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=enzymologie | rel=r_associated | relid=0 | w=20
  502. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> enzymology
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=enzymology | rel=r_associated | relid=0 | w=20
  503. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> épidémiologique
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=épidémiologique | rel=r_associated | relid=0 | w=20
  504. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> ethnologique
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=ethnologique | rel=r_associated | relid=0 | w=20
  505. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> faciès anormal, retard de croissance et retard mental
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=faciès anormal, retard de croissance et retard mental | rel=r_associated | relid=0 | w=20
  506. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> Goltz
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=Goltz | rel=r_associated | relid=0 | w=20
  507. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> histidinémie
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=histidinémie | rel=r_associated | relid=0 | w=20
  508. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> homocarnosinose
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=homocarnosinose | rel=r_associated | relid=0 | w=20
  509. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> hydroxyprolinémie
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=hydroxyprolinémie | rel=r_associated | relid=0 | w=20
  510. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> hyperoxalurie primaire
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=hyperoxalurie primaire | rel=r_associated | relid=0 | w=20
  511. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> hyperoxalurie primitive
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=hyperoxalurie primitive | rel=r_associated | relid=0 | w=20
  512. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> hyperplasie congénitale des surrénales
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=hyperplasie congénitale des surrénales | rel=r_associated | relid=0 | w=20
  513. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> hyperprolinémie
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=hyperprolinémie | rel=r_associated | relid=0 | w=20
  514. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> hyperprolinémie de type I
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=hyperprolinémie de type I | rel=r_associated | relid=0 | w=20
  515. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> hypophosphatasie foetale
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=hypophosphatasie foetale | rel=r_associated | relid=0 | w=20
  516. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> hypophosphatasie infantile
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=hypophosphatasie infantile | rel=r_associated | relid=0 | w=20
  517. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> hypoplasie dermique en aires
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=hypoplasie dermique en aires | rel=r_associated | relid=0 | w=20
  518. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> hypoplasie dermique focale
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=hypoplasie dermique focale | rel=r_associated | relid=0 | w=20
  519. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> idiotie phénylpyruvique
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=idiotie phénylpyruvique | rel=r_associated | relid=0 | w=20
  520. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> intolérance au fructose
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=intolérance au fructose | rel=r_associated | relid=0 | w=20
  521. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> leucinose
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=leucinose | rel=r_associated | relid=0 | w=20
  522. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> lipofuscinose neuronale céroïde
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=lipofuscinose neuronale céroïde | rel=r_associated | relid=0 | w=20
  523. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> lipofuscinose neuronale céroïde infantile finlandaise
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=lipofuscinose neuronale céroïde infantile finlandaise | rel=r_associated | relid=0 | w=20
  524. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> maladie de Wolman
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=maladie de Wolman | rel=r_associated | relid=0 | w=20
  525. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> maladie de wolman
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=maladie de wolman | rel=r_associated | relid=0 | w=20
  526. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> maladie des urines à l'odeur de sirop d'érable
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=maladie des urines à l'odeur de sirop d'érable | rel=r_associated | relid=0 | w=20
  527. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> maladie des urines avec odeur de sirop erable
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=maladie des urines avec odeur de sirop erable | rel=r_associated | relid=0 | w=20
  528. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> maladie du sirop d'érable
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=maladie du sirop d'érable | rel=r_associated | relid=0 | w=20
  529. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> maladie lysosomique de surcharge
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=maladie lysosomique de surcharge | rel=r_associated | relid=0 | w=20
  530. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> microbiologique
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=microbiologique | rel=r_associated | relid=0 | w=20
  531. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> nanisme, retard mental, anomalies oculaires
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=nanisme, retard mental, anomalies oculaires | rel=r_associated | relid=0 | w=20
  532. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> nystagmus congénital isolé
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
  533. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> oligophrénie
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=oligophrénie | rel=r_associated | relid=0 | w=20
  534. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> oxalose
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=oxalose | rel=r_associated | relid=0 | w=20
  535. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> oxalose primitive
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=oxalose primitive | rel=r_associated | relid=0 | w=20
  536. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> oxaloses
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=oxaloses | rel=r_associated | relid=0 | w=20
  537. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> parasitologie
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=parasitologie | rel=r_associated | relid=0 | w=20
  538. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> phénylcétonurie
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=phénylcétonurie | rel=r_associated | relid=0 | w=20
  539. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> progeria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=progeria | rel=r_associated | relid=0 | w=20
  540. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> progéria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=progéria | rel=r_associated | relid=0 | w=20
  541. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> protoproporphyrie érythropoïétique
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=protoproporphyrie érythropoïétique | rel=r_associated | relid=0 | w=20
  542. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> pseudo-hypoparathyroïdie
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=pseudo-hypoparathyroïdie | rel=r_associated | relid=0 | w=20
  543. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> pseudo-hypoparathyroïdisme
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=pseudo-hypoparathyroïdisme | rel=r_associated | relid=0 | w=20
  544. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> pseudohypoparathyroïdie
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=pseudohypoparathyroïdie | rel=r_associated | relid=0 | w=20
  545. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> pseudohypoparathyroïdisme
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=pseudohypoparathyroïdisme | rel=r_associated | relid=0 | w=20
  546. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> psychose présénile
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=psychose présénile | rel=r_associated | relid=0 | w=20
  547. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> psychose sénile
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=psychose sénile | rel=r_associated | relid=0 | w=20
  548. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> retard de croissance
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=retard de croissance | rel=r_associated | relid=0 | w=20
  549. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> retard de croissance staturo-pondérale
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=retard de croissance staturo-pondérale | rel=r_associated | relid=0 | w=20
  550. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> Retard de croissance staturo-pondérale
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=Retard de croissance staturo-pondérale | rel=r_associated | relid=0 | w=20
  551. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> Retard mental
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=Retard mental | rel=r_associated | relid=0 | w=20
  552. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> retard mental
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=retard mental | rel=r_associated | relid=0 | w=20
  553. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> retard mental, retard de croissance, surdité, microgénitalisme lié au sexe
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | rel=r_associated | relid=0 | w=20
  554. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> retardation mentale
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=retardation mentale | rel=r_associated | relid=0 | w=20
  555. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> sénescence sans mention de psychose
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=sénescence sans mention de psychose | rel=r_associated | relid=0 | w=20
  556. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> sénilité
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=sénilité | rel=r_associated | relid=0 | w=20
  557. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> sirop d'érable (urine à odeur de)
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=sirop d'érable (urine à odeur de) | rel=r_associated | relid=0 | w=20
  558. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> syndrome de fragilité du chromosome X
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=syndrome de fragilité du chromosome X | rel=r_associated | relid=0 | w=20
  559. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> syndrome de glissement
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=syndrome de glissement | rel=r_associated | relid=0 | w=20
  560. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> syndrome de Goltz
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=syndrome de Goltz | rel=r_associated | relid=0 | w=20
  561. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> syndrome de goltz
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=syndrome de goltz | rel=r_associated | relid=0 | w=20
  562. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> syndrome de Martin-Bell
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=syndrome de Martin-Bell | rel=r_associated | relid=0 | w=20
  563. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> syndrome de Rett
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=syndrome de Rett | rel=r_associated | relid=0 | w=20
  564. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> syndrome de rett
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=syndrome de rett | rel=r_associated | relid=0 | w=20
  565. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> Syndrome de Rett
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=Syndrome de Rett | rel=r_associated | relid=0 | w=20
  566. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> syndrome du retard de développement
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=syndrome du retard de développement | rel=r_associated | relid=0 | w=20
  567. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> trouble psychotique sénile non précisé
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=trouble psychotique sénile non précisé | rel=r_associated | relid=0 | w=20
  568. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> troubles endocriniens, épilepsie et déficience mentale
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=troubles endocriniens, épilepsie et déficience mentale | rel=r_associated | relid=0 | w=20
  569. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> v+
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=v+ | rel=r_associated | relid=0 | w=20
  570. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> V+
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=V+ | rel=r_associated | relid=0 | w=20
  571. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> vieillesse sans mention de psychose
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=vieillesse sans mention de psychose | rel=r_associated | relid=0 | w=20
  572. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> vomissements
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=vomissements | rel=r_associated | relid=0 | w=20
  573. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 20 / 0.465 -> Wolman (maladie de)
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=Wolman (maladie de) | rel=r_associated | relid=0 | w=20
  574. en:ornithine carbamoyltransferase deficiency disease -- r_associated #0: 1 / 0.023 -> maladie enzymatique
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=maladie enzymatique | rel=r_associated | relid=0 | w=1
≈ 773 relations entrantes

  1. en:maple syrup urine disease --- r_associated #0: 698 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:maple syrup urine disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=698
  2. maladie du sirop d'érable --- r_associated #0: 604.37 --> en:ornithine carbamoyltransferase deficiency disease
    n1=maladie du sirop d'érable | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=604.37
  3. leucinose --- r_associated #0: 599.18 --> en:ornithine carbamoyltransferase deficiency disease
    n1=leucinose | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=599.18
  4. trouble psychotique sénile non précisé --- r_associated #0: 530 --> en:ornithine carbamoyltransferase deficiency disease
    n1=trouble psychotique sénile non précisé | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=530
  5. démence sénile avec delirium ou état confusionnel aigu --- r_associated #0: 525 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence sénile avec delirium ou état confusionnel aigu | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=525
  6. démence forme dépressive ou délirante --- r_associated #0: 520 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence forme dépressive ou délirante | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=520
  7. en:branched-chain ketoaciduria --- r_associated #0: 520 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:branched-chain ketoaciduria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=520
  8. psychose présénile --- r_associated #0: 520 --> en:ornithine carbamoyltransferase deficiency disease
    n1=psychose présénile | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=520
  9. sénescence sans mention de psychose --- r_associated #0: 520 --> en:ornithine carbamoyltransferase deficiency disease
    n1=sénescence sans mention de psychose | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=520
  10. asthénie sénile --- r_associated #0: 518 --> en:ornithine carbamoyltransferase deficiency disease
    n1=asthénie sénile | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=518
  11. débilité sénile --- r_associated #0: 515 --> en:ornithine carbamoyltransferase deficiency disease
    n1=débilité sénile | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=515
  12. démence dégénérative primaire --- r_associated #0: 510 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence dégénérative primaire | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=510
  13. psychose sénile --- r_associated #0: 499 --> en:ornithine carbamoyltransferase deficiency disease
    n1=psychose sénile | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=499
  14. en:senility --- r_associated #0: 480 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:senility | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=480
  15. en:unspecified senile psychotic condition --- r_associated #0: 480 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:unspecified senile psychotic condition | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=480
  16. vieillesse sans mention de psychose --- r_associated #0: 478 --> en:ornithine carbamoyltransferase deficiency disease
    n1=vieillesse sans mention de psychose | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=478
  17. en:senile asthenia --- r_associated #0: 475 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:senile asthenia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=475
  18. démence présénile --- r_associated #0: 461 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence présénile | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=461
  19. en:age-related physical debility --- r_associated #0: 455 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:age-related physical debility | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=455
  20. syndrome de glissement --- r_associated #0: 450 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome de glissement | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=450
  21. démence sénile --- r_associated #0: 445 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence sénile | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=445
  22. en:vomiting --- r_associated #0: 445 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:vomiting | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=445
  23. vomissement --- r_associated #0: 443 --> en:ornithine carbamoyltransferase deficiency disease
    n1=vomissement | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=443
  24. en:presenile dementia --- r_associated #0: 435 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:presenile dementia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=435
  25. sénilité --- r_associated #0: 434 --> en:ornithine carbamoyltransferase deficiency disease
    n1=sénilité | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=434
  26. syndrome de Goltz --- r_associated #0: 401 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome de Goltz | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=401
  27. Goltz --- r_associated #0: 399 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Goltz | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=399
  28. hypoplasie dermique focale --- r_associated #0: 398 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hypoplasie dermique focale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=398
  29. hypoplasie dermique en aires --- r_associated #0: 396 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hypoplasie dermique en aires | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=396
  30. en:focal dermal hypoplasia --- r_associated #0: 395 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:focal dermal hypoplasia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=395
  31. maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 265 --> en:ornithine carbamoyltransferase deficiency disease
    n1=maladie des urines à l'odeur de sirop d'érable | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=265
  32. en:classical maple syrup urine disease --- r_associated #0: 260 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:classical maple syrup urine disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=260
  33. en:thiamin-responsive maple syrup urine disease --- r_associated #0: 260 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:thiamin-responsive maple syrup urine disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=260
  34. maladie des urines avec odeur de sirop erable --- r_associated #0: 260 --> en:ornithine carbamoyltransferase deficiency disease
    n1=maladie des urines avec odeur de sirop erable | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=260
  35. déficit en céto-acide décarboxylase --- r_associated #0: 255 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit en céto-acide décarboxylase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=255
  36. hypophosphatasie infantile --- r_associated #0: 208 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hypophosphatasie infantile | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=208
  37. hypophosphatasie foetale --- r_associated #0: 206 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hypophosphatasie foetale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=206
  38. en:infantile hypophosphatasia --- r_associated #0: 205 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:infantile hypophosphatasia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=205
  39. en:enzymology --- r_associated #0: 201 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:enzymology | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=201
  40. enzymologie --- r_associated #0: 200 --> en:ornithine carbamoyltransferase deficiency disease
    n1=enzymologie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=200
  41. en:pyruvate carboxylase deficiency --- r_associated #0: 175 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:pyruvate carboxylase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=175
  42. déficit en pyruvate carboxylase --- r_associated #0: 173 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit en pyruvate carboxylase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=173
  43. en:parasitology --- r_associated #0: 164 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:parasitology | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=164
  44. enzymology --- r_associated #0: 160 --> en:ornithine carbamoyltransferase deficiency disease
    n1=enzymology | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=160
  45. parasitologie --- r_associated #0: 160 --> en:ornithine carbamoyltransferase deficiency disease
    n1=parasitologie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=160
  46. en:wolman disease --- r_associated #0: 158 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:wolman disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=158
  47. maladie de Wolman --- r_associated #0: 156 --> en:ornithine carbamoyltransferase deficiency disease
    n1=maladie de Wolman | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=156
  48. hyperoxalurie primaire --- r_associated #0: 151 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperoxalurie primaire | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=151
  49. oxaloses --- r_associated #0: 151 --> en:ornithine carbamoyltransferase deficiency disease
    n1=oxaloses | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=151
  50. hyperoxalurie primitive --- r_associated #0: 150 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperoxalurie primitive | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=150
  51. en:primary hyperoxaluria --- r_associated #0: 148 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:primary hyperoxaluria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=148
  52. oxalose primitive --- r_associated #0: 146 --> en:ornithine carbamoyltransferase deficiency disease
    n1=oxalose primitive | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=146
  53. retard de croissance staturo-pondérale --- r_associated #0: 141 --> en:ornithine carbamoyltransferase deficiency disease
    n1=retard de croissance staturo-pondérale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=141
  54. en:pediatric failure to thrive --- r_associated #0: 140 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:pediatric failure to thrive | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=140
  55. oxalose --- r_associated #0: 140 --> en:ornithine carbamoyltransferase deficiency disease
    n1=oxalose | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=140
  56. Retard de croissance staturo-pondérale --- r_associated #0: 135 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Retard de croissance staturo-pondérale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=135
  57. absence de croissance --- r_associated #0: 135 --> en:ornithine carbamoyltransferase deficiency disease
    n1=absence de croissance | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=135
  58. syndrome du retard de développement --- r_associated #0: 135 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome du retard de développement | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=135
  59. en:mental retardation --- r_associated #0: 131 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:mental retardation | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=131
  60. Retard mental --- r_associated #0: 130 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Retard mental | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=130
  61. retard mental --- r_associated #0: 130 --> en:ornithine carbamoyltransferase deficiency disease
    n1=retard mental | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=130
  62. retardation mentale --- r_associated #0: 127 --> en:ornithine carbamoyltransferase deficiency disease
    n1=retardation mentale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=127
  63. en:cytochrome-c oxidase deficiency --- r_associated #0: 114 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:cytochrome-c oxidase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=114
  64. déficit en cytochrome oxydase --- r_associated #0: 112 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit en cytochrome oxydase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=112
  65. vomissements --- r_associated #0: 100 --> en:ornithine carbamoyltransferase deficiency disease
    n1=vomissements | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=100
  66. déficit en cytochrome-c oxydase --- r_associated #0: 95 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit en cytochrome-c oxydase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=95
  67. progeria --- r_associated #0: 95 --> en:ornithine carbamoyltransferase deficiency disease
    n1=progeria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=95
  68. en:progeria --- r_associated #0: 92 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:progeria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=92
  69. progéria --- r_associated #0: 84 --> en:ornithine carbamoyltransferase deficiency disease
    n1=progéria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=84
  70. albinisme --- r_associated #0: 78 --> en:ornithine carbamoyltransferase deficiency disease
    n1=albinisme | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=78
  71. en:muscular dystrophy, emery-dreifuss --- r_associated #0: 77 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:muscular dystrophy, emery-dreifuss | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=77
  72. dystrophie musculaire d'Emery-Dreifuss --- r_associated #0: 76 --> en:ornithine carbamoyltransferase deficiency disease
    n1=dystrophie musculaire d'Emery-Dreifuss | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=76
  73. en:albinism --- r_associated #0: 74 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:albinism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=74
  74. en:emery-dreifuss muscular dystrophy --- r_associated #0: 73 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:emery-dreifuss muscular dystrophy | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=73
  75. arriération mentale --- r_associated #0: 71 --> en:ornithine carbamoyltransferase deficiency disease
    n1=arriération mentale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=71
  76. débilité mentale --- r_associated #0: 70 --> en:ornithine carbamoyltransferase deficiency disease
    n1=débilité mentale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=70
  77. retard de croissance --- r_associated #0: 70 --> en:ornithine carbamoyltransferase deficiency disease
    n1=retard de croissance | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=70
  78. en:hemophilia b --- r_associated #0: 62 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hemophilia b | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=62
  79. pseudo-hypoparathyroïdie --- r_associated #0: 62 --> en:ornithine carbamoyltransferase deficiency disease
    n1=pseudo-hypoparathyroïdie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=62
  80. pseudohypoparathyroïdie --- r_associated #0: 60 --> en:ornithine carbamoyltransferase deficiency disease
    n1=pseudohypoparathyroïdie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=60
  81. congénitale --- r_associated #0: 58 --> en:ornithine carbamoyltransferase deficiency disease
    n1=congénitale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=58
  82. en:hemophilia B --- r_associated #0: 58 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hemophilia B | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=58
  83. en:congenital --- r_associated #0: 57 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:congenital | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=57
  84. en:pseudohypoparathyroidism --- r_associated #0: 55 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:pseudohypoparathyroidism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=55
  85. pseudo-hypoparathyroïdisme --- r_associated #0: 55 --> en:ornithine carbamoyltransferase deficiency disease
    n1=pseudo-hypoparathyroïdisme | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=55
  86. pseudohypoparathyroïdisme --- r_associated #0: 54 --> en:ornithine carbamoyltransferase deficiency disease
    n1=pseudohypoparathyroïdisme | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=54
  87. en:glutaric acidemia type 1 --- r_associated #0: 53 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glutaric acidemia type 1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=53
  88. congenital --- r_associated #0: 52 --> en:ornithine carbamoyltransferase deficiency disease
    n1=congenital | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=52
  89. congénital --- r_associated #0: 52 --> en:ornithine carbamoyltransferase deficiency disease
    n1=congénital | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=52
  90. Syndrome de Rett --- r_associated #0: 50 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Syndrome de Rett | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=50
  91. acidurie glutarique de type 1 --- r_associated #0: 50 --> en:ornithine carbamoyltransferase deficiency disease
    n1=acidurie glutarique de type 1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=50
  92. en:Wolman's disease --- r_associated #0: 50 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:Wolman's disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=50
  93. en:rett syndrome --- r_associated #0: 50 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:rett syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=50
  94. retard mental, retard de croissance, surdité, microgénitalisme lié au sexe --- r_associated #0: 50 --> en:ornithine carbamoyltransferase deficiency disease
    n1=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=50
  95. syndrome de Rett --- r_associated #0: 50 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome de Rett | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=50
  96. dystrophie musculaire d'emery-dreifuss --- r_associated #0: 49 --> en:ornithine carbamoyltransferase deficiency disease
    n1=dystrophie musculaire d'emery-dreifuss | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=49
  97. maladie de wolman --- r_associated #0: 48 --> en:ornithine carbamoyltransferase deficiency disease
    n1=maladie de wolman | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=48
  98. syndrome de goltz --- r_associated #0: 48 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome de goltz | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=48
  99. syndrome de rett --- r_associated #0: 48 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome de rett | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=48
  100. acidémie glutarique de type 1 --- r_associated #0: 46 --> en:ornithine carbamoyltransferase deficiency disease
    n1=acidémie glutarique de type 1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=46
  101. dyskératose congénitale --- r_associated #0: 45 --> en:ornithine carbamoyltransferase deficiency disease
    n1=dyskératose congénitale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=45
  102. déliquescence --- r_associated #0: 43 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déliquescence | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=43
  103. en:lissencephaly, x-linked, 2 --- r_associated #0: 43 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:lissencephaly, x-linked, 2 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=43
  104. en:ornithine carbamoyl phosphate deficiency --- r_associated #0: 43 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ornithine carbamoyl phosphate deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=43
  105. en:norrie syndrome --- r_associated #0: 42 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:norrie syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=42
  106. en:sulfite oxidase deficiency --- r_associated #0: 42 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:sulfite oxidase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=42
  107. en:vrozené poruchy metabolismu nec in mdrcze18_1 --- r_associated #0: 42 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:vrozené poruchy metabolismu nec in mdrcze18_1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=42
  108. hyperphénylalaninémie --- r_associated #0: 42 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperphénylalaninémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=42
  109. sirop d'érable (urine à odeur de) --- r_associated #0: 42 --> en:ornithine carbamoyltransferase deficiency disease
    n1=sirop d'érable (urine à odeur de) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=42
  110. déficit en semialdéhyde succinique-déshydrogénase --- r_associated #0: 41 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit en semialdéhyde succinique-déshydrogénase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=41
  111. en:complication aspects --- r_associated #0: 41 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:complication aspects | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=41
  112. en:congenital nephrogenic diabetes insipidus --- r_associated #0: 41 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:congenital nephrogenic diabetes insipidus | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=41
  113. en:disorder of amino acid and organic acid metabolism --- r_associated #0: 41 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:disorder of amino acid and organic acid metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=41
  114. en:disorder of glycosaminoglycan metabolism --- r_associated #0: 41 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:disorder of glycosaminoglycan metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=41
  115. protoproporphyrie érythropoïétique --- r_associated #0: 41 --> en:ornithine carbamoyltransferase deficiency disease
    n1=protoproporphyrie érythropoïétique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=41
  116. v+ --- r_associated #0: 41 --> en:ornithine carbamoyltransferase deficiency disease
    n1=v+ | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=41
  117. V+ --- r_associated #0: 40 --> en:ornithine carbamoyltransferase deficiency disease
    n1=V+ | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=40
  118. déficit en ornithinecarbamyl-transférase --- r_associated #0: 40 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit en ornithinecarbamyl-transférase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=40
  119. en:fraxe intellectual disability syndrome --- r_associated #0: 40 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:fraxe intellectual disability syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=40
  120. en:hnsha due to hexokinase deficiency --- r_associated #0: 40 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hnsha due to hexokinase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=40
  121. en:purine-pyrimidine metabolism, inborn errors --- r_associated #0: 40 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:purine-pyrimidine metabolism, inborn errors | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=40
  122. en:senile dementia --- r_associated #0: 40 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:senile dementia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=40
  123. en:succinic semialdehyde dehydrogenase deficiency --- r_associated #0: 40 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:succinic semialdehyde dehydrogenase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=40
  124. en:ugt1a1*28 polymorphism --- r_associated #0: 40 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ugt1a1*28 polymorphism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=40
  125. intolérance au fructose --- r_associated #0: 40 --> en:ornithine carbamoyltransferase deficiency disease
    n1=intolérance au fructose | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=40
  126. nanisme, retard mental, anomalies oculaires --- r_associated #0: 40 --> en:ornithine carbamoyltransferase deficiency disease
    n1=nanisme, retard mental, anomalies oculaires | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=40
  127. déficit en ornithine-carbamyl-transférase --- r_associated #0: 39 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit en ornithine-carbamyl-transférase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=39
  128. en:Goltz syndrome --- r_associated #0: 39 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:Goltz syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=39
  129. en:aminomethyltransferase deficiency --- r_associated #0: 39 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:aminomethyltransferase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=39
  130. en:muscle d-lactate dehydrogenase deficiency --- r_associated #0: 39 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:muscle d-lactate dehydrogenase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=39
  131. en:pelizaeus-merzbacher disease --- r_associated #0: 39 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:pelizaeus-merzbacher disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=39
  132. en:x chromosome-linked pyridoxine refractory sideroblastic anemia --- r_associated #0: 39 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x chromosome-linked pyridoxine refractory sideroblastic anemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=39
  133. hyperprolinémie --- r_associated #0: 39 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperprolinémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=39
  134. maladie lysosomique de surcharge --- r_associated #0: 39 --> en:ornithine carbamoyltransferase deficiency disease
    n1=maladie lysosomique de surcharge | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=39
  135. microbiologique --- r_associated #0: 39 --> en:ornithine carbamoyltransferase deficiency disease
    n1=microbiologique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=39
  136. nystagmus congénital isolé --- r_associated #0: 39 --> en:ornithine carbamoyltransferase deficiency disease
    n1=nystagmus congénital isolé | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=39
  137. en:x-linked adrenal hypoplasia congenita --- r_associated #0: 38 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked adrenal hypoplasia congenita | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=38
  138. faciès anormal, retard de croissance et retard mental --- r_associated #0: 38 --> en:ornithine carbamoyltransferase deficiency disease
    n1=faciès anormal, retard de croissance et retard mental | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=38
  139. lipofuscinose neuronale céroïde --- r_associated #0: 38 --> en:ornithine carbamoyltransferase deficiency disease
    n1=lipofuscinose neuronale céroïde | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=38
  140. déficit en ornithine-transcarbamylase --- r_associated #0: 37 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit en ornithine-transcarbamylase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=37
  141. en:ataxia, fatal x-linked, with deafness and loss of vision --- r_associated #0: 37 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ataxia, fatal x-linked, with deafness and loss of vision | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=37
  142. en:erythropoietic protoporphyria --- r_associated #0: 37 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:erythropoietic protoporphyria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=37
  143. en:hypophosphatasia infantile --- r_associated #0: 37 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hypophosphatasia infantile | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=37
  144. en:roentgenographic --- r_associated #0: 37 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:roentgenographic | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=37
  145. en:urea cycle metabolism disorder --- r_associated #0: 37 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:urea cycle metabolism disorder | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=37
  146. en:glutaric aciduria, type 1 --- r_associated #0: 36 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glutaric aciduria, type 1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=36
  147. en:hereditary fructose intolerance --- r_associated #0: 36 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hereditary fructose intolerance | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=36
  148. en:hyperprolinemia --- r_associated #0: 36 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperprolinemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=36
  149. en:inherited disorder of thyroid metabolism --- r_associated #0: 36 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:inherited disorder of thyroid metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=36
  150. en:microbiological --- r_associated #0: 36 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:microbiological | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=36
  151. en:phenylketonuria --- r_associated #0: 36 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:phenylketonuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=36
  152. Wolman (maladie de) --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Wolman (maladie de) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  153. déficit en ornithine carbamyltransférase --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit en ornithine carbamyltransférase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  154. en:biotinidase deficiency --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:biotinidase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  155. en:childhood cerebral x-linked adrenoleukodystrophy --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:childhood cerebral x-linked adrenoleukodystrophy | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  156. en:congenital adrenal hyperplasia --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:congenital adrenal hyperplasia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  157. en:dermoids of cornea --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:dermoids of cornea | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  158. en:dihydropyrimidine dehydrogenase deficiency --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:dihydropyrimidine dehydrogenase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  159. en:disorder of creatine synthesis --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:disorder of creatine synthesis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  160. en:disorder of sialic acid metabolism --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:disorder of sialic acid metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  161. en:glutamate formiminotransferase deficiency --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glutamate formiminotransferase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  162. en:glutamate-cysteine ligase deficiency --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glutamate-cysteine ligase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  163. en:glycogen storage disease type viii --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glycogen storage disease type viii | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  164. en:high urinary orotic acid --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:high urinary orotic acid | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  165. en:homocarnosinosis --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:homocarnosinosis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  166. en:hyper-igm immunodeficiency syndrome, type 1 --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyper-igm immunodeficiency syndrome, type 1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  167. en:hyperhomocysteinemia --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperhomocysteinemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  168. en:lysosomal storage disease --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:lysosomal storage disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  169. en:mental deficiency --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:mental deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  170. en:microphthalmia, syndromic 1 --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:microphthalmia, syndromic 1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  171. en:microphthalmia, syndromic 4 (disorder) --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:microphthalmia, syndromic 4 (disorder) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  172. en:moloney syndrome --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:moloney syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  173. en:myoglobinuria, recurrent --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:myoglobinuria, recurrent | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  174. en:ocular albinism, type ii --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ocular albinism, type ii | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  175. en:placental steroid sulfatase deficiency --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:placental steroid sulfatase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  176. en:porphobilinogen synthase deficiency --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:porphobilinogen synthase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  177. en:sex chromosome disorders of sex development --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:sex chromosome disorders of sex development | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  178. en:steroid metabolism, inborn errors --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:steroid metabolism, inborn errors | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  179. en:stroke (rare) --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:stroke (rare) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  180. en:x-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  181. hyperplasie congénitale des surrénales --- r_associated #0: 35 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperplasie congénitale des surrénales | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=35
  182. en:acute hyperammonemia --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:acute hyperammonemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  183. en:allan-herndon-dudley syndrome --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:allan-herndon-dudley syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  184. en:alpha, alpha-trehalase deficiency --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:alpha, alpha-trehalase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  185. en:amino acid deficiency --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:amino acid deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  186. en:circulating enzyme deficiency --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:circulating enzyme deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  187. en:congenital sucrase-isomaltase deficiency --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:congenital sucrase-isomaltase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  188. en:developmental delay --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:developmental delay | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  189. en:dmd-associated dilated cardiomyopathy --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:dmd-associated dilated cardiomyopathy | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  190. en:episodic ataxia --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:episodic ataxia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  191. en:gaucher disease --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:gaucher disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  192. en:genetic diseases, x-linked --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:genetic diseases, x-linked | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  193. en:glutathione synthetase deficiency --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glutathione synthetase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  194. en:high ornithine --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:high ornithine | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  195. en:hydroxykynureninuria --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hydroxykynureninuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  196. en:hypermethioniuria --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hypermethioniuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  197. en:inborn error of lipoprotein metabolism --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:inborn error of lipoprotein metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  198. en:isolated noncompaction of the ventricular myocardium --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:isolated noncompaction of the ventricular myocardium | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  199. en:low plasma arginine --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:low plasma arginine | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  200. en:lubs x-linked mental retardation syndrome --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:lubs x-linked mental retardation syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  201. en:lysinuric protein intolerance --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:lysinuric protein intolerance | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  202. en:maple-tree syrup disease --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:maple-tree syrup disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  203. en:mental retardation with psychosis, pyramidal signs, and macroorchidism --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:mental retardation with psychosis, pyramidal signs, and macroorchidism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  204. en:mental retardation, x-linked, snyder-robinson type --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:mental retardation, x-linked, snyder-robinson type | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  205. en:methylmalonyl-coenzyme a mutase deficiency --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:methylmalonyl-coenzyme a mutase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  206. en:neuronal ceroid lipofuscinosis --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:neuronal ceroid lipofuscinosis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  207. en:other specified disorders of amino-acid transport and metabolism --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:other specified disorders of amino-acid transport and metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  208. en:pancreatic alpha-amylase deficiency --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:pancreatic alpha-amylase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  209. en:unclassified metabolic disorder --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:unclassified metabolic disorder | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  210. en:x-linked lymphoproliferative syndrome --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked lymphoproliferative syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  211. idiotie phénylpyruvique --- r_associated #0: 34 --> en:ornithine carbamoyltransferase deficiency disease
    n1=idiotie phénylpyruvique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  212. lipofuscinose neuronale céroïde infantile finlandaise --- r_associated #0: 33 --> en:ornithine carbamoyltransferase deficiency disease
    n1=lipofuscinose neuronale céroïde infantile finlandaise | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=33
  213. déficience intellectuelle --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficience intellectuelle | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  214. en:adolescent x-linked adrenoleukodystrophy --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:adolescent x-linked adrenoleukodystrophy | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  215. en:alpha-1 antitrypsin deficiency --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:alpha-1 antitrypsin deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  216. en:amino acid metabolism disorder --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:amino acid metabolism disorder | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  217. en:angiokeratoma corporis diffusum --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:angiokeratoma corporis diffusum | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  218. en:arakawa syndrome ii --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:arakawa syndrome ii | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  219. en:argininemia --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:argininemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  220. en:carbamoyl-phosphate synthetase i deficiency --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:carbamoyl-phosphate synthetase i deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  221. en:dent's disease --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:dent's disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  222. en:hereditary methemoglobinemia, enzymatic type --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hereditary methemoglobinemia, enzymatic type | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  223. en:hyperammonemia --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperammonemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  224. en:lesch-nyhan syndrome --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:lesch-nyhan syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  225. en:leucinosis --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:leucinosis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  226. en:lipid metabolism disorder --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:lipid metabolism disorder | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  227. en:lipoid congenital adrenal hyperplasia --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:lipoid congenital adrenal hyperplasia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  228. en:methylene thf reductase deficiency and homocystinuria --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:methylene thf reductase deficiency and homocystinuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  229. en:moderate steroid 21-hydroxylase deficiency --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:moderate steroid 21-hydroxylase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  230. en:ohdo syndrome, maat-kievit-brunner type --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ohdo syndrome, maat-kievit-brunner type | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  231. en:opitz g/bbb syndrome --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:opitz g/bbb syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  232. en:partington x-linked mental retardation syndrome --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:partington x-linked mental retardation syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  233. en:pediatric terminology --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:pediatric terminology | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  234. en:periventricular heterotopia, x-linked --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:periventricular heterotopia, x-linked | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  235. en:urocanase deficiency --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:urocanase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  236. en:valinemia --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:valinemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  237. en:x-linked bulbar-muscular atrophy --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked bulbar-muscular atrophy | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  238. en:x-linked severe combined immunodeficiency --- r_associated #0: 32 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked severe combined immunodeficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  239. déficit en ornithine transcarbamylase --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit en ornithine transcarbamylase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  240. en:5 alpha steroid reductase 2 deficiency --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:5 alpha steroid reductase 2 deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  241. en:acquired lactase deficiency --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:acquired lactase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  242. en:carbohydrate metabolism, inborn errors --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:carbohydrate metabolism, inborn errors | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  243. en:choroideremia --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:choroideremia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  244. en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  245. en:cystathionine beta-synthase deficiency disease --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:cystathionine beta-synthase deficiency disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  246. en:ethanolaminosis --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ethanolaminosis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  247. en:etiology aspects --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:etiology aspects | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  248. en:gamma-glutamyltransferase deficiency --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:gamma-glutamyltransferase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  249. en:glycogen storage disease --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glycogen storage disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  250. en:glycogen storage disease type iib --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glycogen storage disease type iib | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  251. en:glycogen storage disease type vi --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glycogen storage disease type vi | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  252. en:hyperandrogenism due to non-classic 21-hydroxylase deficiency --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperandrogenism due to non-classic 21-hydroxylase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  253. en:hyperphenylalaninemia, non phenylketonuric --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperphenylalaninemia, non phenylketonuric | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  254. en:inborn errors of bilirubin metabolism --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:inborn errors of bilirubin metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  255. en:inborn errors of porphyrin metabolism --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:inborn errors of porphyrin metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  256. en:masa syndrome (disorder) --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:masa syndrome (disorder) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  257. en:menkes disease --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:menkes disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  258. en:mental retardation, x-linked --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:mental retardation, x-linked | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  259. en:mental retardation, x-linked, syndromic, christianson type --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:mental retardation, x-linked, syndromic, christianson type | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  260. en:multiple acyl-coa dehydrogenase deficiency --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:multiple acyl-coa dehydrogenase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  261. en:orofaciodigital syndromes --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:orofaciodigital syndromes | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  262. en:other disturbances of straight-chain amino-acid metabolism --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:other disturbances of straight-chain amino-acid metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  263. en:premature aging syndrome --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:premature aging syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  264. en:pyridoxine dependency syndrome --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:pyridoxine dependency syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  265. histidinémie --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histidinémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  266. homocarnosinose --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=homocarnosinose | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  267. hyperprolinémie de type I --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperprolinémie de type I | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  268. oligophrénie --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=oligophrénie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  269. syndrome de Martin-Bell --- r_associated #0: 31 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome de Martin-Bell | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
  270. arriération --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=arriération | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  271. carence en ornithine carbamoyltransférase --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=carence en ornithine carbamoyltransférase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  272. démence (sémiologie) --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence (sémiologie) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  273. en:5-oxoprolinase deficiency --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:5-oxoprolinase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  274. en:Gaucher disease --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:Gaucher disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  275. en:alkaptonuria --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:alkaptonuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  276. en:amino acid/carbohydrate metabolic disorder --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:amino acid/carbohydrate metabolic disorder | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  277. en:androgen insensitivity syndrome --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:androgen insensitivity syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  278. en:aspects of radionuclide imaging --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:aspects of radionuclide imaging | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  279. en:beta-methylcrotonylglycinuria --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:beta-methylcrotonylglycinuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  280. en:carrier females may present with postpartum hyperammonemia --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:carrier females may present with postpartum hyperammonemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  281. en:craniofrontonasal dysplasia --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:craniofrontonasal dysplasia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  282. en:disorder of aromatic amino acid metabolism --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:disorder of aromatic amino acid metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  283. en:disorder of histidine metabolism --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:disorder of histidine metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  284. en:disorder of pyruvate metabolism and mitochondrial respiratory chain --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:disorder of pyruvate metabolism and mitochondrial respiratory chain | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  285. en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  286. en:emesia --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:emesia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  287. en:emesis --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:emesis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  288. en:epidemiologic --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:epidemiologic | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  289. en:fragile X syndrome --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:fragile X syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  290. en:fragile x syndrome --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:fragile x syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  291. en:hereditary xanthinuria --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hereditary xanthinuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  292. en:histidinaemia --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:histidinaemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  293. en:hmg-coa lyase deficiency --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hmg-coa lyase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  294. en:inborn errors of steroid synthesis --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:inborn errors of steroid synthesis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  295. en:inherited disorder of folate metabolism --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:inherited disorder of folate metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  296. en:lactase deficiency, congenital --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:lactase deficiency, congenital | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  297. en:learning disability --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:learning disability | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  298. en:lecithin acyltransferase deficiency --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:lecithin acyltransferase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  299. en:mental handicap --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:mental handicap | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  300. en:molybdenum cofactor deficiency --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:molybdenum cofactor deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  301. en:muscle amp deaminase deficiency --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:muscle amp deaminase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  302. en:muscle l-lactate dehydrogenase deficiency --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:muscle l-lactate dehydrogenase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  303. en:nance-horan syndrome --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:nance-horan syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  304. en:neonatal research network terminology --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:neonatal research network terminology | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  305. en:nystagmus --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:nystagmus | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  306. en:otc, glu87lys --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, glu87lys | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  307. en:otc, gly162arg --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, gly162arg | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  308. en:otc, gly47glu --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, gly47glu | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  309. en:otc, gt-gc, intron 7 --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, gt-gc, intron 7 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  310. en:otc, gta-gtg, intron 7 --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, gta-gtg, intron 7 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  311. en:otc, ivs2, g-a, -1 --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, ivs2, g-a, -1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  312. en:peroxisomal disorder --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:peroxisomal disorder | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  313. en:radiotherapeutic --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:radiotherapeutic | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  314. en:respiratory alkalosis --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:respiratory alkalosis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  315. en:retardation --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:retardation | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  316. en:seizure --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:seizure | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  317. en:specific enzyme deficiency --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:specific enzyme deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  318. en:x-linked dystonia parkinsonism --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked dystonia parkinsonism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  319. syndrome de fragilité du chromosome X --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome de fragilité du chromosome X | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  320. épidémiologique --- r_associated #0: 30 --> en:ornithine carbamoyltransferase deficiency disease
    n1=épidémiologique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
  321. carence en ornithine transcarbamylase --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=carence en ornithine transcarbamylase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  322. contractures congénitales et arachnodactylie --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=contractures congénitales et arachnodactylie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  323. déficience mentale --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficience mentale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  324. en:2-hydroxyglutaric aciduria --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:2-hydroxyglutaric aciduria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  325. en:aicardi syndrome --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:aicardi syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  326. en:arginosuccinate lyase deficiency --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:arginosuccinate lyase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  327. en:asymptomatic hyperammonemia --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:asymptomatic hyperammonemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  328. en:brain diseases, metabolic, inborn --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:brain diseases, metabolic, inborn | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  329. en:crigler-najjar syndrome --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:crigler-najjar syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  330. en:deficiency of steryl-sulfatase --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:deficiency of steryl-sulfatase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  331. en:disorder due to cytochrome p450 enzyme variant --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:disorder due to cytochrome p450 enzyme variant | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  332. en:disorder due to n-acetyltransferase enzyme variant --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:disorder due to n-acetyltransferase enzyme variant | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  333. en:disorder of ornithine metabolism --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:disorder of ornithine metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  334. en:duchenne muscular dystrophy --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:duchenne muscular dystrophy | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  335. en:dyserythropoietic anemia with thrombocytopenia --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:dyserythropoietic anemia with thrombocytopenia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  336. en:enterokinase deficiency --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:enterokinase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  337. en:epidemiological --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:epidemiological | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  338. en:failure of the mind --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:failure of the mind | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  339. en:familial renal iminoglycinuria --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:familial renal iminoglycinuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  340. en:fanconi syndrome --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:fanconi syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  341. en:feeble-mindedness --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:feeble-mindedness | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  342. en:hartnup disease --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hartnup disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  343. en:holoprosencephaly with fetal akinesia-hypokinesia sequence --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  344. en:hyperglutaminemia --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperglutaminemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  345. en:hyperlipoproteinemia type I --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperlipoproteinemia type I | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  346. en:hyperprolinemia type 1 --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperprolinemia type 1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  347. en:intermediary metabolism disorder --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:intermediary metabolism disorder | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  348. en:lipid metabolism, inborn errors --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:lipid metabolism, inborn errors | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  349. en:mental dullness --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:mental dullness | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  350. en:methylmalonic acidemia --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:methylmalonic acidemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  351. en:microcephaly microcornea syndrome seemanova type --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:microcephaly microcornea syndrome seemanova type | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  352. en:microphthalmia, syndromic 2 --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:microphthalmia, syndromic 2 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  353. en:morosis --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:morosis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  354. en:nursing therapy --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:nursing therapy | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  355. en:ornithine carbamoyltransferase deficiency --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ornithine carbamoyltransferase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  356. en:ornithine carbamoyltransferase:ccnc:pt:ser:qn --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ornithine carbamoyltransferase:ccnc:pt:ser:qn | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  357. en:otc, leu272phe --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, leu272phe | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  358. en:other disorders of aromatic amino-acid metabolism --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:other disorders of aromatic amino-acid metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  359. en:other specified disorders of amino-acid metabolism --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:other specified disorders of amino-acid metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  360. en:pancreatic colipase deficiency --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:pancreatic colipase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  361. en:phenylpyruvic oligophrenia --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:phenylpyruvic oligophrenia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  362. en:physiopathological --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:physiopathological | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  363. en:renal aminoacidurias --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:renal aminoacidurias | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  364. en:renpenning syndrome 1 --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:renpenning syndrome 1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  365. en:storage disease --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:storage disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  366. en:thyroid dyshormonogenesis 4 --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:thyroid dyshormonogenesis 4 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  367. en:transitory amino acid metabolic disorder --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:transitory amino acid metabolic disorder | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  368. en:tyrosinemia type II --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:tyrosinemia type II | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  369. en:tyrosinemia type ii --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:tyrosinemia type ii | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  370. en:wiskott-aldrich syndrome --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:wiskott-aldrich syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  371. en:x-linked agammaglobulinemia --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked agammaglobulinemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  372. en:x-linked creatine transporter deficiency --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked creatine transporter deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  373. en:x-linked dyskeratosis congenita --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked dyskeratosis congenita | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  374. en:x-linked hydrocephalus syndrome --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked hydrocephalus syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  375. en:x-linked recessive --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked recessive | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  376. phénylcétonurie --- r_associated #0: 29 --> en:ornithine carbamoyltransferase deficiency disease
    n1=phénylcétonurie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=29
  377. en:adrenal gland hyperplasia ii --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:adrenal gland hyperplasia ii | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  378. en:barth syndrome --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:barth syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  379. en:beta-aminoisobutyricaciduria --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:beta-aminoisobutyricaciduria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  380. en:borjeson-forssman-lehmann syndrome --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:borjeson-forssman-lehmann syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  381. en:brunner syndrome --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:brunner syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  382. en:coma --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:coma | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  383. en:defect in post-translational modification of lysosomal enzymes --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:defect in post-translational modification of lysosomal enzymes | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  384. en:dihydrouracil dehydrogenase deficiency --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:dihydrouracil dehydrogenase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  385. en:disorder of branched-chain amino acid metabolism --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:disorder of branched-chain amino acid metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  386. en:ehlers-danlos syndrome, arthrochalasia type --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ehlers-danlos syndrome, arthrochalasia type | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  387. en:familial amyloidosis --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:familial amyloidosis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  388. en:galactosemia --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:galactosemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  389. en:genetic aspects --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:genetic aspects | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  390. en:glucose-6-phosphate dehydrogenase deficiency anemia --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glucose-6-phosphate dehydrogenase deficiency anemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  391. en:hepatic ornithine transcarbamylase deficiency --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hepatic ornithine transcarbamylase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  392. en:hereditary hyperbilirubinemia --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hereditary hyperbilirubinemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  393. en:hereditary orotic aciduria --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hereditary orotic aciduria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  394. en:high plasma asparagine --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:high plasma asparagine | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  395. en:hydrocephalus with cerebellar agenesis --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hydrocephalus with cerebellar agenesis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  396. en:hypophosphatasia --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hypophosphatasia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  397. en:in blood --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:in blood | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  398. en:in cerebrospinal fluid --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:in cerebrospinal fluid | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  399. en:inborn lipid/lipoprotein disorder --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:inborn lipid/lipoprotein disorder | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  400. en:lactose intolerance, adult type --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:lactose intolerance, adult type | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  401. en:mohr-tranebjaerg syndrome --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:mohr-tranebjaerg syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  402. en:multiple carboxylase deficiency --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:multiple carboxylase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  403. en:nutritional management --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:nutritional management | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  404. en:oligergasia --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:oligergasia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  405. en:otc, arg109gln --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, arg109gln | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  406. en:otc, arg26gln --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, arg26gln | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  407. en:otc, arg62thr --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, arg62thr | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  408. en:otc, del --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, del | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  409. en:otc, gln216glu --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, gln216glu | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  410. en:otc, leu111pro --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, leu111pro | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  411. en:pentosuria --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:pentosuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  412. en:phenylketonuria ii --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:phenylketonuria ii | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  413. en:therapeutic aspects --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:therapeutic aspects | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  414. en:type I --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:type I | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  415. en:tyrosinemia, type iii --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:tyrosinemia, type iii | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  416. ethnologique --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=ethnologique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  417. hyperammoniémie de type ii --- r_associated #0: 28 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperammoniémie de type ii | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=28
  418. en:X-linked --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:X-linked | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  419. en:alpha thalassemia x-linked mental retardation syndrome --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:alpha thalassemia x-linked mental retardation syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  420. en:amino acid transport disorders, inborn --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:amino acid transport disorders, inborn | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  421. en:aminoaciduria --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:aminoaciduria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  422. en:anhidrotic ectodermal dysplasia 1 --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:anhidrotic ectodermal dysplasia 1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  423. en:argininosuccinic aciduria --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:argininosuccinic aciduria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  424. en:butyryl-coa dehydrogenase deficiency --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:butyryl-coa dehydrogenase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  425. en:carnitine palmitoyltransferase deficiency --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:carnitine palmitoyltransferase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  426. en:cask related intellectual disability --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:cask related intellectual disability | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  427. en:caused by mutation in the ornithine transcarbamylase gene (otc, 311250.0001) --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:caused by mutation in the ornithine transcarbamylase gene (otc, 311250.0001) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  428. en:chronic granulomatous disease --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:chronic granulomatous disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  429. en:conditions tested for in this newborn screening study:id:pt:bld.dot:nom --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:conditions tested for in this newborn screening study:id:pt:bld.dot:nom | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  430. en:congenital pancreatic enterokinase deficiency --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:congenital pancreatic enterokinase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  431. en:deficiency in enzyme complexes of mitochondrial respiratory chain --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:deficiency in enzyme complexes of mitochondrial respiratory chain | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  432. en:deficiency of fructokinase --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:deficiency of fructokinase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  433. en:disorder of lysine and hydroxylysine metabolism --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:disorder of lysine and hydroxylysine metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  434. en:disorder of sulfur-bearing amino acid metabolism --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:disorder of sulfur-bearing amino acid metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  435. en:ethnologic --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ethnologic | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  436. en:fatty acid metabolism disorder --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:fatty acid metabolism disorder | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  437. en:glutathione s-transferase deficiency --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glutathione s-transferase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  438. en:glycine dehydrogenase (decarboxylating) deficiency --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glycine dehydrogenase (decarboxylating) deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  439. en:histidinemia --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:histidinemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  440. en:hyperglycinemia --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperglycinemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  441. en:hyperlipoproteinemia type i --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperlipoproteinemia type i | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  442. en:hyperphenylalaninemia --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperphenylalaninemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  443. en:in urine --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:in urine | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  444. en:inborn biological transport disorder --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:inborn biological transport disorder | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  445. en:isovaleric acidemia --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:isovaleric acidemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  446. en:methionine adenosyltransferase deficiency --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:methionine adenosyltransferase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  447. en:methylcrotonyl-coa carboxylase deficiency --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:methylcrotonyl-coa carboxylase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  448. en:n-acetylglutamate synthase deficiency --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:n-acetylglutamate synthase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  449. en:oligopsychia --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:oligopsychia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  450. en:otc, gly50ter --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, gly50ter | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  451. en:otc, pro225leu --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, pro225leu | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  452. en:oxalosis --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:oxalosis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  453. en:prevalence of 1 in 40,000 to 1 in 80,000 --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:prevalence of 1 in 40,000 to 1 in 80,000 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  454. en:psychology qualifier --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:psychology qualifier | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  455. en:purine-nucleoside phosphorylase deficiency --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:purine-nucleoside phosphorylase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  456. en:pyruvate kinase deficiency --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:pyruvate kinase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  457. en:sarcosinemia --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:sarcosinemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  458. en:simpson golabi behmel syndrome type 1 --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:simpson golabi behmel syndrome type 1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  459. en:spondyloepiphyseal dysplasia tarda, x-linked --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:spondyloepiphyseal dysplasia tarda, x-linked | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  460. en:veterinary aspects --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:veterinary aspects | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  461. en:viruses --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:viruses | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  462. en:waisman syndrome --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:waisman syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  463. en:x-linked ichthyosis --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked ichthyosis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  464. troubles endocriniens, épilepsie et déficience mentale --- r_associated #0: 27 --> en:ornithine carbamoyltransferase deficiency disease
    n1=troubles endocriniens, épilepsie et déficience mentale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=27
  465. cétoacidurie à chaînes ramifiées --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=cétoacidurie à chaînes ramifiées | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  466. dyslipémie --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=dyslipémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  467. déficit en prolidase --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit en prolidase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  468. en:amino acidemia disorder suspected:prid:pt:bld.dot:nom --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:amino acidemia disorder suspected:prid:pt:bld.dot:nom | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  469. en:aspects of mortality statistics --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:aspects of mortality statistics | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  470. en:beta thalassemia x-linked thrombocytopenia syndrome --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:beta thalassemia x-linked thrombocytopenia syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  471. en:cerebral edema --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:cerebral edema | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  472. en:chemically induced --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:chemically induced | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  473. en:childhood hypophosphatasia (disorder) --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  474. en:dihydropyrimidinase deficiency --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:dihydropyrimidinase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  475. en:disorder of glycoprotein metabolism --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:disorder of glycoprotein metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  476. en:folinic acid responsive seizure syndrome --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:folinic acid responsive seizure syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  477. en:glucose-6-phosphate dehydrogenase deficiency --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glucose-6-phosphate dehydrogenase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  478. en:glycogen storage disease type x --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glycogen storage disease type x | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  479. en:hemophilia A --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hemophilia A | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  480. en:hemophilia a --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hemophilia a | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  481. en:holocarboxylase synthetase deficiency --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:holocarboxylase synthetase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  482. en:homocystinemia --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:homocystinemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  483. en:homocystinuria --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:homocystinuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  484. en:hunter syndrome --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hunter syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  485. en:hydroxyprolinemia --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hydroxyprolinemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  486. en:hyperinsulinemic hypoglycemia, familial, 6 --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperinsulinemic hypoglycemia, familial, 6 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  487. en:hyperlysinemia --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperlysinemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  488. en:inborn errors of carbohydrate metabolism (excl glucose) --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:inborn errors of carbohydrate metabolism (excl glucose) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  489. en:increased aromatase activity --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:increased aromatase activity | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  490. en:irritation --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:irritation | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  491. en:juvenile x-linked retinoschisis --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:juvenile x-linked retinoschisis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  492. en:low plasma citrulline --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:low plasma citrulline | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  493. en:lujan fryns syndrome --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:lujan fryns syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  494. en:methylmalonic aciduria --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:methylmalonic aciduria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  495. en:newborn conditions with positive markers:prid:pt:bld.dot:nom --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:newborn conditions with positive markers:prid:pt:bld.dot:nom | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  496. en:ocular albinism type 1 --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ocular albinism type 1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  497. en:otc, 1-bp del, 403g --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, 1-bp del, 403g | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  498. en:otc, arg129his --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, arg129his | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  499. en:otc, arg40cys --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, arg40cys | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  500. en:otc, tyr313asp --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, tyr313asp | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  501. en:other disorders of urea cycle metabolism --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:other disorders of urea cycle metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  502. en:pancreatic trypsinogen deficiency --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:pancreatic trypsinogen deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  503. en:pharmacotherapeutic --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:pharmacotherapeutic | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  504. en:prolidase deficiency --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:prolidase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  505. en:propionic acidemia --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:propionic acidemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  506. en:pyruvate dehydrogenase deficiency --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:pyruvate dehydrogenase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  507. en:two types - lethal neonatal and less severe, late onset --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:two types - lethal neonatal and less severe, late onset | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  508. en:x-linked lissencephaly --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked lissencephaly | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  509. en:x-linked retinal dysplasia --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked retinal dysplasia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  510. hydroxyprolinémie --- r_associated #0: 26 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hydroxyprolinémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  511. albinisme avec pigmentation minime --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=albinisme avec pigmentation minime | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  512. albinisme oculaire de type 1 --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=albinisme oculaire de type 1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  513. en:17 alpha-hydroxyprogesterone aldolase deficiency --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:17 alpha-hydroxyprogesterone aldolase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  514. en:Martin-Bell's syndrome --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:Martin-Bell's syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  515. en:clinical spectrum in males ranges from lethal neonatal onset to milder forms with first recognized episode in late childhood or even in adulthood --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:clinical spectrum in males ranges from lethal neonatal onset to milder forms with first recognized episode in late childhood or even in adulthood | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  516. en:embryologic --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:embryologic | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  517. en:episodic ammonia intoxication --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:episodic ammonia intoxication | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  518. en:hnsha due to nadh diaphorase deficiency --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hnsha due to nadh diaphorase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  519. en:inherited disorder of bilirubin metabolism --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:inherited disorder of bilirubin metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  520. en:newborn conditions with equivocal markers:prid:pt:bld.dot:nom --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:newborn conditions with equivocal markers:prid:pt:bld.dot:nom | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  521. en:oculocerebrorenal syndrome --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:oculocerebrorenal syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  522. en:oligophrenia --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:oligophrenia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  523. en:organic acid metabolism disorder --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:organic acid metabolism disorder | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  524. en:otc, arg109ter --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, arg109ter | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  525. en:otc, leu45pro --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, leu45pro | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  526. en:pathological aspects --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:pathological aspects | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  527. en:severe steroid 21-hydroxylase deficiency --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:severe steroid 21-hydroxylase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  528. en:use of ultrasonography --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:use of ultrasonography | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  529. en:vomitus --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:vomitus | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  530. hémophilie B --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hémophilie B | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  531. radiographique --- r_associated #0: 25 --> en:ornithine carbamoyltransferase deficiency disease
    n1=radiographique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=25
  532. albinisme oculocutané de type mutant jaune --- r_associated #0: 24 --> en:ornithine carbamoyltransferase deficiency disease
    n1=albinisme oculocutané de type mutant jaune | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=24
  533. cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie --- r_associated #0: 24 --> en:ornithine carbamoyltransferase deficiency disease
    n1=cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=24
  534. en:cystinosis --- r_associated #0: 24 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:cystinosis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=24
  535. en:cystinuria --- r_associated #0: 24 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:cystinuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=24
  536. en:diagnosis aspect --- r_associated #0: 24 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:diagnosis aspect | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=24
  537. en:dyskeratosis congenita --- r_associated #0: 24 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:dyskeratosis congenita | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=24
  538. en:ferrochelatase deficiency --- r_associated #0: 24 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ferrochelatase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=24
  539. en:hyperornithinemia --- r_associated #0: 24 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperornithinemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=24
  540. en:immunology aspects --- r_associated #0: 24 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:immunology aspects | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=24
  541. en:inborn error of glutathione metabolism --- r_associated #0: 24 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:inborn error of glutathione metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=24
  542. en:ornithine carbamoyltransferase:ccnc:pt:amnio fld:qn --- r_associated #0: 24 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ornithine carbamoyltransferase:ccnc:pt:amnio fld:qn | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=24
  543. en:otc, arg40his --- r_associated #0: 24 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, arg40his | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=24
  544. en:renal tubular transport, inborn errors --- r_associated #0: 24 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:renal tubular transport, inborn errors | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=24
  545. en:transient hyperammonemia in infancy --- r_associated #0: 24 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:transient hyperammonemia in infancy | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=24
  546. en:17-beta-hydroxysteroid dehydrogenase 3 deficiency --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:17-beta-hydroxysteroid dehydrogenase 3 deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  547. en:5' 10' methylenetetrahydrofolate reductase deficiency --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:5' 10' methylenetetrahydrofolate reductase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  548. en:adult hypophosphatasia (disorder) --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:adult hypophosphatasia (disorder) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  549. en:amino acid transport disorder --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:amino acid transport disorder | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  550. en:benign neonatal hyperaminoaciduria --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:benign neonatal hyperaminoaciduria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  551. en:exposure as collected domain --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:exposure as collected domain | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  552. en:female restricted epilepsy with intellectual disability syndrome --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:female restricted epilepsy with intellectual disability syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  553. en:fructose-1,6-bisphosphatase deficiency --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:fructose-1,6-bisphosphatase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  554. en:historical aspects qualifier --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:historical aspects qualifier | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  555. en:inherited metabolic disorder of nervous system --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:inherited metabolic disorder of nervous system | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  556. en:intestinal disaccharidase deficiency --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:intestinal disaccharidase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  557. en:lethargy --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:lethargy | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  558. en:metabolic aspects --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:metabolic aspects | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  559. en:ornithine carbamoyltransferase --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ornithine carbamoyltransferase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  560. en:otc, arg277trp --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, arg277trp | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  561. en:protein avoidance --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:protein avoidance | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  562. en:tyrosinemia --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:tyrosinemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  563. semialdéhyde succinique-déshydrogénase (déficit en) --- r_associated #0: 23 --> en:ornithine carbamoyltransferase deficiency disease
    n1=semialdéhyde succinique-déshydrogénase (déficit en) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=23
  564. Goltz (syndrome de) --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Goltz (syndrome de) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  565. Maladie de Wolman --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Maladie de Wolman | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  566. déficit en biotinidase --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit en biotinidase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  567. déficit en sulfite-oxydase --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit en sulfite-oxydase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  568. en:acetyl-coa: carboxylase deficiency --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:acetyl-coa: carboxylase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  569. en:acyl-coa dehydrogenase deficiency --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:acyl-coa dehydrogenase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  570. en:aldosterone synthase deficiency --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:aldosterone synthase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  571. en:and microgenitalism --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:and microgenitalism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  572. en:cerebellar atrophy --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:cerebellar atrophy | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  573. en:citrullinemia --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:citrullinemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  574. en:dwarfism --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:dwarfism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  575. en:glutaric aciduria type 1 --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glutaric aciduria type 1 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  576. en:glycine encephalopathy --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glycine encephalopathy | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  577. en:juvenile cataract --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:juvenile cataract | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  578. en:methylenetetrahydrofolate reductase deficiency --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:methylenetetrahydrofolate reductase deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  579. en:otc, arg245trp --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, arg245trp | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  580. en:otc, glu154ter --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, glu154ter | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  581. en:otc, ivs4, a-t, -2 --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, ivs4, a-t, -2 | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  582. en:rehabilitation aspects --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:rehabilitation aspects | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  583. en:some carrier females have episodes of significant hyperammonemia in infancy or childhood --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:some carrier females have episodes of significant hyperammonemia in infancy or childhood | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  584. en:surgical aspects --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:surgical aspects | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  585. en:wolman's disease --- r_associated #0: 22 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:wolman's disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  586. Déficience intellectuelle --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Déficience intellectuelle | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  587. acidurie argininosuccinique --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=acidurie argininosuccinique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  588. acidémie isovalérique --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=acidémie isovalérique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  589. albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  590. alcaptonurie --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=alcaptonurie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  591. argininémie --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=argininémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  592. cataracte-atrophie du cervelet-myopathie --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=cataracte-atrophie du cervelet-myopathie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  593. choroïdérémie --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=choroïdérémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  594. déficit enzymatique partiel de la surrénale --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit enzymatique partiel de la surrénale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  595. en:Mohr-Tranebjaerg syndrome --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:Mohr-Tranebjaerg syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  596. en:classical phenylketonuria --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:classical phenylketonuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  597. en:deafness --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:deafness | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  598. en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  599. en:inborn immunodeficiency --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:inborn immunodeficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  600. en:metal metabolism, inborn errors --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:metal metabolism, inborn errors | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  601. en:methylenetetrahydrofolate reductase gene mutation --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:methylenetetrahydrofolate reductase gene mutation | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  602. en:otc, leu148phe --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, leu148phe | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  603. en:otc, met206arg --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:otc, met206arg | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  604. en:phosphoglycerate kinase 1 deficiency --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:phosphoglycerate kinase 1 deficiency | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  605. en:taxonomic --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:taxonomic | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  606. en:with growth retardation --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:with growth retardation | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  607. en:x-linked epilepsy with learning disability and behavior disorder syndrome --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:x-linked epilepsy with learning disability and behavior disorder syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  608. glycogénose --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=glycogénose | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  609. idiosyncrasie au fructose --- r_associated #0: 21 --> en:ornithine carbamoyltransferase deficiency disease
    n1=idiosyncrasie au fructose | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  610. Sénilité --- r_associated #0: 20 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Sénilité | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=20
  611. maladie --- r_associated #0: 20 --> en:ornithine carbamoyltransferase deficiency disease
    n1=maladie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=20
  612. Albert (position d') --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Albert (position d') | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  613. Arrhenius (loi d') --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Arrhenius (loi d') | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  614. Enzymologie --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Enzymologie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  615. His (faisceau de) --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=His (faisceau de) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  616. Hyperplasie congénitale des surrénales --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Hyperplasie congénitale des surrénales | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  617. Intolérance au fructose --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Intolérance au fructose | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  618. Parasitologie --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Parasitologie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  619. Vomissement --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Vomissement | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  620. acidoses lactiques (classification selon Cohen et Woods) --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=acidoses lactiques (classification selon Cohen et Woods) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  621. coma
    (médecine)
     --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=coma
    (médecine)
    | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  622. goltz --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=goltz | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  623. handicap mental --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=handicap mental | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  624. hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  625. hyperpression fémoropatellaire latérale (syndrome d') --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperpression fémoropatellaire latérale (syndrome d') | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  626. hypophosphatasie --- r_associated #0: 15 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hypophosphatasie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=15
  627. syndrome de Zinsser-Engman-Cole --- r_associated #0: 11 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome de Zinsser-Engman-Cole | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=11
  628. Albinisme --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Albinisme | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  629. CONGÉNITALE --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=CONGÉNITALE | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  630. Déficience mentale --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Déficience mentale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  631. Glycogénose --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Glycogénose | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  632. Histidinémie --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Histidinémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  633. Martin-Bell (syndrome de) --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Martin-Bell (syndrome de) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  634. Paraquat ® (intoxication par le) --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Paraquat ® (intoxication par le) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  635. Phénylcétonurie --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Phénylcétonurie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  636. Progéria --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Progéria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  637. Retard de croissance --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Retard de croissance | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  638. Sengstaken-Blakemore (sonde de) --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Sengstaken-Blakemore (sonde de) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  639. VOMISSEMENTS --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=VOMISSEMENTS | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  640. Vomissements --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Vomissements | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  641. Völker-Dieben (atrophie optique liée au sexe de) --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Völker-Dieben (atrophie optique liée au sexe de) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  642. Went (atrophie optique liée au sexe de) --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Went (atrophie optique liée au sexe de) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  643. alcalose métabolique (classification) --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=alcalose métabolique (classification) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  644. coma --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=coma | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  645. cornée et tyrosinose de type II --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=cornée et tyrosinose de type II | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  646. de type I --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=de type I | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  647. déficit en phosphatases alcalines --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit en phosphatases alcalines | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  648. déficit intellectuel --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=déficit intellectuel | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  649. démence d'Alzheimer --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence d'Alzheimer | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  650. démence frontotemporale --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence frontotemporale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  651. démence héréditaire et infarctus multiples cérébraux --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence héréditaire et infarctus multiples cérébraux | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  652. démence myoclonique --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence myoclonique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  653. démence parkinsonienne avec dégénérescence pallidopontonigrée --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence parkinsonienne avec dégénérescence pallidopontonigrée | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  654. démence précoce --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence précoce | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  655. démence pugilistique --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence pugilistique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  656. démence régressive --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence régressive | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  657. démence sémantique --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence sémantique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  658. en:Albert's position --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:Albert's position | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  659. en:Arrhenius'law --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:Arrhenius'law | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  660. en:Dent's disease --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:Dent's disease | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  661. en:HHH syndrome --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:HHH syndrome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  662. en:alcaptonuria --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:alcaptonuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  663. en:and growth retardation --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:and growth retardation | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  664. en:contractural arachnodactyly --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:contractural arachnodactyly | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  665. en:dyslipaemia --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:dyslipaemia | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  666. en:endocrine disorder --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:endocrine disorder | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  667. en:ethnological --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:ethnological | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  668. en:eye abnormality --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:eye abnormality | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  669. en:glycogenosis --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:glycogenosis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  670. en:haemophilia B --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:haemophilia B | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  671. en:homogentisuria --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:homogentisuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  672. en:hyperornithinemia hyperammoniemia homocitrullinuria --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperornithinemia hyperammoniemia homocitrullinuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  673. en:hyperprolinemia. --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:hyperprolinemia. | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  674. en:infantile finnish type --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:infantile finnish type | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  675. en:intellectual disability --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:intellectual disability | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  676. en:minimal pigment type --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:minimal pigment type | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  677. en:radiographic --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:radiographic | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  678. en:unusual facies --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=en:unusual facies | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  679. faciale (paralysie du nouveau-né) --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=faciale (paralysie du nouveau-né) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  680. glycogénique (surcharge et infiltration) --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=glycogénique (surcharge et infiltration) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  681. hyperlipoprotéinémie de type I --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperlipoprotéinémie de type I | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  682. hypophosphatasies --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hypophosphatasies | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  683. hémophilie A --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hémophilie A | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  684. maladie de Gaucher --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=maladie de Gaucher | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  685. nanisme --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=nanisme | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  686. neurofibromatose de type périphérique --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=neurofibromatose de type périphérique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  687. nystagmus --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=nystagmus | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  688. nystagmus héréditaire vertical --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=nystagmus héréditaire vertical | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  689. nystagmus lié au sexe --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=nystagmus lié au sexe | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  690. nystagmus myoclonies --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=nystagmus myoclonies | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  691. profondeur de l'anesthésie (stade de) --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=profondeur de l'anesthésie (stade de) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  692. prolidase (déficit en) --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=prolidase (déficit en) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  693. retards de croissance et de développement avec dysmorphie faciale --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=retards de croissance et de développement avec dysmorphie faciale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  694. rétinite pigmentaire, surdité, retard mental, et hypogonadisme --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=rétinite pigmentaire, surdité, retard mental, et hypogonadisme | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  695. sirtuine --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=sirtuine | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  696. sisi-test --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=sisi-test | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  697. sismothérapie --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=sismothérapie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  698. surdité --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=surdité | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  699. syndrome cataracte-ataxie-surdité et retard mental --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome cataracte-ataxie-surdité et retard mental | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  700. syndrome de Bridges et Good --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome de Bridges et Good | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  701. syndrome de Mohr-Tranebjaerg --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome de Mohr-Tranebjaerg | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  702. syndrome de Rathbun --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome de Rathbun | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  703. syndrome de Treft-Sanborn-Carey --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome de Treft-Sanborn-Carey | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  704. taxinomique --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=taxinomique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  705. trichomégalie avec retard mental, nanisme, et dégénérescence pigmentée de la rétine --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=trichomégalie avec retard mental, nanisme, et dégénérescence pigmentée de la rétine | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  706. urticaire-surdité-amylose rénale --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=urticaire-surdité-amylose rénale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  707. xanthomatose familiale primitive --- r_associated #0: 10 --> en:ornithine carbamoyltransferase deficiency disease
    n1=xanthomatose familiale primitive | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=10
  708. ARRX --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=ARRX | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  709. Acinetobacter --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Acinetobacter | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  710. Handicap mental --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Handicap mental | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  711. Microbiologique --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=Microbiologique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  712. acidurie --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=acidurie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  713. acidurie 3-hydroxy-3-méthyl-glutarique --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=acidurie 3-hydroxy-3-méthyl-glutarique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  714. acidurie 3-méthylglutaconique --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=acidurie 3-méthylglutaconique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  715. acidurie 4-hydroxybutyrique --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=acidurie 4-hydroxybutyrique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  716. acidurie paradoxale --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=acidurie paradoxale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  717. acineux --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=acineux | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  718. acini --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=acini | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  719. acinus --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=acinus | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  720. acinus hépatique de Rappaport --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=acinus hépatique de Rappaport | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  721. albinisme avec immunodéficience et troubles hématologiques --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=albinisme avec immunodéficience et troubles hématologiques | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  722. albinisme avec surdité --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=albinisme avec surdité | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  723. arrière-pied --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=arrière-pied | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  724. démence alcoolique --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence alcoolique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  725. démence aluminique --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence aluminique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  726. démence sous-corticale --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence sous-corticale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  727. démence sénile de type Alzheimer --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence sénile de type Alzheimer | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  728. démence sénile mixte --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence sénile mixte | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  729. démence traumatique --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence traumatique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  730. démence vasculaire --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence vasculaire | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  731. démence vésanique --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence vésanique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  732. démence à corps de Lewy --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démence à corps de Lewy | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  733. démences et prions --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=démences et prions | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  734. faisceau de His --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=faisceau de His | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  735. histaminergie --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histaminergie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  736. histaminergique --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histaminergique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  737. histaminique --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histaminique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  738. histaminolibération --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histaminolibération | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  739. histaminolytique --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histaminolytique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  740. histaminopexie --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histaminopexie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  741. histaminurie --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histaminurie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  742. histaminémie --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histaminémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  743. histidase --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histidase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  744. histidinase --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histidinase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  745. histidine --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histidine | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  746. histidine-ammoniac-lyase --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histidine-ammoniac-lyase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  747. histidine-décarboxylase --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histidine-décarboxylase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  748. histidine-désaminase --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=histidine-désaminase | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  749. hyperostose vertébrale ankylosante --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperostose vertébrale ankylosante | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  750. hyperoxalurie --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperoxalurie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  751. hyperoxalémie --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperoxalémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  752. hyperprolactinémie --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperprolactinémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  753. hyperprothrombinémie --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperprothrombinémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  754. hyperprotidémie --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperprotidémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  755. hyperprotéinorachie --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperprotéinorachie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  756. hyperprotéinémie --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperprotéinémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  757. hyperptyalisme --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperptyalisme | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  758. hyperpyruvicémie --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=hyperpyruvicémie | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  759. nystagmus (zone de moindre) --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=nystagmus (zone de moindre) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  760. semidominance --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=semidominance | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  761. semiquinone --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=semiquinone | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  762. syndrome d'hyperpression fémoropatellaire latérale --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=syndrome d'hyperpression fémoropatellaire latérale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  763. séminal --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=séminal | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  764. séminifère --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=séminifère | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  765. séminomateux --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=séminomateux | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  766. séminome --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=séminome | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  767. séminome de l'ovaire --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=séminome de l'ovaire | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  768. séminome du médiastin --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=séminome du médiastin | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  769. séminome spermatocytaire --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=séminome spermatocytaire | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  770. sémiochimique --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=sémiochimique | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  771. sémiologie extrapyramidale --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=sémiologie extrapyramidale | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  772. troubles héréditaires du transport tubulaire rénal --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=troubles héréditaires du transport tubulaire rénal | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
  773. vomitus --- r_associated #0: 5 --> en:ornithine carbamoyltransferase deficiency disease
    n1=vomitus | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=5
Le service Rézo permet d'énumérer les relations existant pour un terme. Ce service est interrogeable par programme.
Projet JeuxDeMots - url: http://www.jeuxdemots.org
contact: mathieu.lafourcade@lirmm.fr