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'en:classical phenylketonuria'
(id=6813114 ; fe=en:classical phenylketonuria ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=80609.28002929688 creation date=2017-06-25 touchdate=2025-09-13 23:18:04.000)
≈ 1258 relations sortantes

  1. en:classical phenylketonuria -- r_associated #0: 43 / 1 -> en:amino acid metabolism disorder
    n1=en:classical phenylketonuria | n2=en:amino acid metabolism disorder | rel=r_associated | relid=0 | w=43
  2. en:classical phenylketonuria -- r_associated #0: 42 / 0.977 -> en:disorder of aromatic amino acid metabolism
    n1=en:classical phenylketonuria | n2=en:disorder of aromatic amino acid metabolism | rel=r_associated | relid=0 | w=42
  3. en:classical phenylketonuria -- r_associated #0: 42 / 0.977 -> idiotie phénylpyruvique
    n1=en:classical phenylketonuria | n2=idiotie phénylpyruvique | rel=r_associated | relid=0 | w=42
  4. en:classical phenylketonuria -- r_associated #0: 40 / 0.93 -> en:angelman syndrome
    n1=en:classical phenylketonuria | n2=en:angelman syndrome | rel=r_associated | relid=0 | w=40
  5. en:classical phenylketonuria -- r_associated #0: 38 / 0.884 -> en:profound intellectual disabilities
    n1=en:classical phenylketonuria | n2=en:profound intellectual disabilities | rel=r_associated | relid=0 | w=38
  6. en:classical phenylketonuria -- r_associated #0: 35 / 0.814 -> en:alpha-1 antitrypsin deficiency
    n1=en:classical phenylketonuria | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=35
  7. en:classical phenylketonuria -- r_associated #0: 35 / 0.814 -> en:cystinuria
    n1=en:classical phenylketonuria | n2=en:cystinuria | rel=r_associated | relid=0 | w=35
  8. en:classical phenylketonuria -- r_associated #0: 35 / 0.814 -> en:histidinemia
    n1=en:classical phenylketonuria | n2=en:histidinemia | rel=r_associated | relid=0 | w=35
  9. en:classical phenylketonuria -- r_associated #0: 35 / 0.814 -> en:pseudohypoparathyroidism
    n1=en:classical phenylketonuria | n2=en:pseudohypoparathyroidism | rel=r_associated | relid=0 | w=35
  10. en:classical phenylketonuria -- r_associated #0: 35 / 0.814 -> en:tyrosinemia
    n1=en:classical phenylketonuria | n2=en:tyrosinemia | rel=r_associated | relid=0 | w=35
  11. en:classical phenylketonuria -- r_associated #0: 34 / 0.791 -> en:oculocerebrorenal syndrome
    n1=en:classical phenylketonuria | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=34
  12. en:classical phenylketonuria -- r_associated #0: 34 / 0.791 -> imbécilité phénylpyruvique
    n1=en:classical phenylketonuria | n2=imbécilité phénylpyruvique | rel=r_associated | relid=0 | w=34
  13. en:classical phenylketonuria -- r_associated #0: 34 / 0.791 -> phénylcétonurie de type 1
    n1=en:classical phenylketonuria | n2=phénylcétonurie de type 1 | rel=r_associated | relid=0 | w=34
  14. en:classical phenylketonuria -- r_associated #0: 34 / 0.791 -> phénylcétonuries
    n1=en:classical phenylketonuria | n2=phénylcétonuries | rel=r_associated | relid=0 | w=34
  15. en:classical phenylketonuria -- r_associated #0: 32 / 0.744 -> en:cardiac and circulatory congenital anomalies
    n1=en:classical phenylketonuria | n2=en:cardiac and circulatory congenital anomalies | rel=r_associated | relid=0 | w=32
  16. en:classical phenylketonuria -- r_associated #0: 32 / 0.744 -> en:inborn immunodeficiency
    n1=en:classical phenylketonuria | n2=en:inborn immunodeficiency | rel=r_associated | relid=0 | w=32
  17. en:classical phenylketonuria -- r_associated #0: 32 / 0.744 -> en:maple syrup urine disease
    n1=en:classical phenylketonuria | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=32
  18. en:classical phenylketonuria -- r_associated #0: 32 / 0.744 -> en:nutritional and metabolic diseases
    n1=en:classical phenylketonuria | n2=en:nutritional and metabolic diseases | rel=r_associated | relid=0 | w=32
  19. en:classical phenylketonuria -- r_associated #0: 31 / 0.721 -> en:biliary atresia
    n1=en:classical phenylketonuria | n2=en:biliary atresia | rel=r_associated | relid=0 | w=31
  20. en:classical phenylketonuria -- r_associated #0: 31 / 0.721 -> en:congenital visceral anomaly
    n1=en:classical phenylketonuria | n2=en:congenital visceral anomaly | rel=r_associated | relid=0 | w=31
  21. en:classical phenylketonuria -- r_associated #0: 31 / 0.721 -> en:intellectual disability
    n1=en:classical phenylketonuria | n2=en:intellectual disability | rel=r_associated | relid=0 | w=31
  22. en:classical phenylketonuria -- r_associated #0: 31 / 0.721 -> en:isovaleric acidemia
    n1=en:classical phenylketonuria | n2=en:isovaleric acidemia | rel=r_associated | relid=0 | w=31
  23. en:classical phenylketonuria -- r_associated #0: 31 / 0.721 -> phénylcétonurie de type i
    n1=en:classical phenylketonuria | n2=phénylcétonurie de type i | rel=r_associated | relid=0 | w=31
  24. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> déficit grave en phénylalanine hydroxylase
    n1=en:classical phenylketonuria | n2=déficit grave en phénylalanine hydroxylase | rel=r_associated | relid=0 | w=30
  25. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:3-methylglutaconic aciduria type 3
    n1=en:classical phenylketonuria | n2=en:3-methylglutaconic aciduria type 3 | rel=r_associated | relid=0 | w=30
  26. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:adult fanconi syndrome
    n1=en:classical phenylketonuria | n2=en:adult fanconi syndrome | rel=r_associated | relid=0 | w=30
  27. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:cerebellar ataxia ectodermal dysplasia
    n1=en:classical phenylketonuria | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=30
  28. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:chromaturia
    n1=en:classical phenylketonuria | n2=en:chromaturia | rel=r_associated | relid=0 | w=30
  29. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:congenital
    n1=en:classical phenylketonuria | n2=en:congenital | rel=r_associated | relid=0 | w=30
  30. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:congenital adrenal hyperplasia
    n1=en:classical phenylketonuria | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=30
  31. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:congenital deformity of labyrinth
    n1=en:classical phenylketonuria | n2=en:congenital deformity of labyrinth | rel=r_associated | relid=0 | w=30
  32. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:congenital deformity of pharynx
    n1=en:classical phenylketonuria | n2=en:congenital deformity of pharynx | rel=r_associated | relid=0 | w=30
  33. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:congenital hypoplasia of genital tubercle
    n1=en:classical phenylketonuria | n2=en:congenital hypoplasia of genital tubercle | rel=r_associated | relid=0 | w=30
  34. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:crisponi syndrome
    n1=en:classical phenylketonuria | n2=en:crisponi syndrome | rel=r_associated | relid=0 | w=30
  35. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:cryoglobulinuria
    n1=en:classical phenylketonuria | n2=en:cryoglobulinuria | rel=r_associated | relid=0 | w=30
  36. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:cytochrome-c oxidase deficiency
    n1=en:classical phenylketonuria | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=30
  37. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:desmosterolosis
    n1=en:classical phenylketonuria | n2=en:desmosterolosis | rel=r_associated | relid=0 | w=30
  38. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:ectodermal dysplasia
    n1=en:classical phenylketonuria | n2=en:ectodermal dysplasia | rel=r_associated | relid=0 | w=30
  39. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:enterokinase deficiency
    n1=en:classical phenylketonuria | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=30
  40. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:ethanolaminosis
    n1=en:classical phenylketonuria | n2=en:ethanolaminosis | rel=r_associated | relid=0 | w=30
  41. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:familial acantholysis
    n1=en:classical phenylketonuria | n2=en:familial acantholysis | rel=r_associated | relid=0 | w=30
  42. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:familial renal iminoglycinuria
    n1=en:classical phenylketonuria | n2=en:familial renal iminoglycinuria | rel=r_associated | relid=0 | w=30
  43. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:fragile x syndrome
    n1=en:classical phenylketonuria | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=30
  44. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:gaucher disease
    n1=en:classical phenylketonuria | n2=en:gaucher disease | rel=r_associated | relid=0 | w=30
  45. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:gracile syndrome (disorder)
    n1=en:classical phenylketonuria | n2=en:gracile syndrome (disorder) | rel=r_associated | relid=0 | w=30
  46. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:hereditary orotic aciduria
    n1=en:classical phenylketonuria | n2=en:hereditary orotic aciduria | rel=r_associated | relid=0 | w=30
  47. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:hyperchloruria
    n1=en:classical phenylketonuria | n2=en:hyperchloruria | rel=r_associated | relid=0 | w=30
  48. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:intestinal malrotation
    n1=en:classical phenylketonuria | n2=en:intestinal malrotation | rel=r_associated | relid=0 | w=30
  49. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:laurence-moon syndrome
    n1=en:classical phenylketonuria | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=30
  50. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:lesch-nyhan syndrome
    n1=en:classical phenylketonuria | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=30
  51. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:lysosomal storage disease
    n1=en:classical phenylketonuria | n2=en:lysosomal storage disease | rel=r_associated | relid=0 | w=30
  52. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:macdermot winter syndrome
    n1=en:classical phenylketonuria | n2=en:macdermot winter syndrome | rel=r_associated | relid=0 | w=30
  53. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:mowat-wilson syndrome
    n1=en:classical phenylketonuria | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=30
  54. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:myopathy with exercise intolerance, swedish type
    n1=en:classical phenylketonuria | n2=en:myopathy with exercise intolerance, swedish type | rel=r_associated | relid=0 | w=30
  55. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:neuronal ceroid lipofuscinosis
    n1=en:classical phenylketonuria | n2=en:neuronal ceroid lipofuscinosis | rel=r_associated | relid=0 | w=30
  56. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:neutral lipid storage disease with myopathy
    n1=en:classical phenylketonuria | n2=en:neutral lipid storage disease with myopathy | rel=r_associated | relid=0 | w=30
  57. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:oculocerebral hypopigmentation syndrome type preus
    n1=en:classical phenylketonuria | n2=en:oculocerebral hypopigmentation syndrome type preus | rel=r_associated | relid=0 | w=30
  58. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:other mental retardation
    n1=en:classical phenylketonuria | n2=en:other mental retardation | rel=r_associated | relid=0 | w=30
  59. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:phosphoglycerate kinase 1 deficiency
    n1=en:classical phenylketonuria | n2=en:phosphoglycerate kinase 1 deficiency | rel=r_associated | relid=0 | w=30
  60. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:primary hyperoxaluria
    n1=en:classical phenylketonuria | n2=en:primary hyperoxaluria | rel=r_associated | relid=0 | w=30
  61. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:prolidase deficiency
    n1=en:classical phenylketonuria | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=30
  62. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:prosoposchisis
    n1=en:classical phenylketonuria | n2=en:prosoposchisis | rel=r_associated | relid=0 | w=30
  63. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:smith-magenis syndrome
    n1=en:classical phenylketonuria | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=30
  64. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:spinocerebellar ataxia with epilepsy
    n1=en:classical phenylketonuria | n2=en:spinocerebellar ataxia with epilepsy | rel=r_associated | relid=0 | w=30
  65. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:thomas syndrome
    n1=en:classical phenylketonuria | n2=en:thomas syndrome | rel=r_associated | relid=0 | w=30
  66. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:tmem70 related mitochondrial encephalo-cardio-myopathy
    n1=en:classical phenylketonuria | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=30
  67. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:traumatic hematuria
    n1=en:classical phenylketonuria | n2=en:traumatic hematuria | rel=r_associated | relid=0 | w=30
  68. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:trichohepatoenteric syndrome
    n1=en:classical phenylketonuria | n2=en:trichohepatoenteric syndrome | rel=r_associated | relid=0 | w=30
  69. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> en:xeroderma pigmentosum
    n1=en:classical phenylketonuria | n2=en:xeroderma pigmentosum | rel=r_associated | relid=0 | w=30
  70. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> goût
    n1=en:classical phenylketonuria | n2=goût | rel=r_associated | relid=0 | w=30
  71. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> maladie génétique
    n1=en:classical phenylketonuria | n2=maladie génétique | rel=r_associated | relid=0 | w=30
  72. en:classical phenylketonuria -- r_associated #0: 30 / 0.698 -> oligophrénie phénylpyruvique
    n1=en:classical phenylketonuria | n2=oligophrénie phénylpyruvique | rel=r_associated | relid=0 | w=30
  73. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> anomalie congénitale
    n1=en:classical phenylketonuria | n2=anomalie congénitale | rel=r_associated | relid=0 | w=29
  74. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:alpha-methylacyl-coa racemase deficiency
    n1=en:classical phenylketonuria | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=29
  75. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:alpha, alpha-trehalase deficiency
    n1=en:classical phenylketonuria | n2=en:alpha, alpha-trehalase deficiency | rel=r_associated | relid=0 | w=29
  76. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:anomaly congenital special senses
    n1=en:classical phenylketonuria | n2=en:anomaly congenital special senses | rel=r_associated | relid=0 | w=29
  77. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:argininemia
    n1=en:classical phenylketonuria | n2=en:argininemia | rel=r_associated | relid=0 | w=29
  78. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:brody myopathy
    n1=en:classical phenylketonuria | n2=en:brody myopathy | rel=r_associated | relid=0 | w=29
  79. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:cardiovascular abnormalities
    n1=en:classical phenylketonuria | n2=en:cardiovascular abnormalities | rel=r_associated | relid=0 | w=29
  80. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:cheilognathoschisis
    n1=en:classical phenylketonuria | n2=en:cheilognathoschisis | rel=r_associated | relid=0 | w=29
  81. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:chitty hall baraitser syndrome
    n1=en:classical phenylketonuria | n2=en:chitty hall baraitser syndrome | rel=r_associated | relid=0 | w=29
  82. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:cleft lip
    n1=en:classical phenylketonuria | n2=en:cleft lip | rel=r_associated | relid=0 | w=29
  83. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:cohen syndrome
    n1=en:classical phenylketonuria | n2=en:cohen syndrome | rel=r_associated | relid=0 | w=29
  84. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:common atrioventricular orifice in double inlet ventricle
    n1=en:classical phenylketonuria | n2=en:common atrioventricular orifice in double inlet ventricle | rel=r_associated | relid=0 | w=29
  85. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:congenital abnormality
    n1=en:classical phenylketonuria | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=29
  86. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:congenital abnormality of lower limb and/or pelvic girdle
    n1=en:classical phenylketonuria | n2=en:congenital abnormality of lower limb and/or pelvic girdle | rel=r_associated | relid=0 | w=29
  87. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:congenital anomaly of trunk
    n1=en:classical phenylketonuria | n2=en:congenital anomaly of trunk | rel=r_associated | relid=0 | w=29
  88. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:congenital deformity of chest wall
    n1=en:classical phenylketonuria | n2=en:congenital deformity of chest wall | rel=r_associated | relid=0 | w=29
  89. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:crigler-najjar syndrome
    n1=en:classical phenylketonuria | n2=en:crigler-najjar syndrome | rel=r_associated | relid=0 | w=29
  90. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:crystalluria
    n1=en:classical phenylketonuria | n2=en:crystalluria | rel=r_associated | relid=0 | w=29
  91. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:cystinosis
    n1=en:classical phenylketonuria | n2=en:cystinosis | rel=r_associated | relid=0 | w=29
  92. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:dicarboxylicaminoaciduria
    n1=en:classical phenylketonuria | n2=en:dicarboxylicaminoaciduria | rel=r_associated | relid=0 | w=29
  93. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:down syndrome
    n1=en:classical phenylketonuria | n2=en:down syndrome | rel=r_associated | relid=0 | w=29
  94. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:eczema
    n1=en:classical phenylketonuria | n2=en:eczema | rel=r_associated | relid=0 | w=29
  95. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:epiphyseal dysplasia, multiple, 4
    n1=en:classical phenylketonuria | n2=en:epiphyseal dysplasia, multiple, 4 | rel=r_associated | relid=0 | w=29
  96. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:faecaluria
    n1=en:classical phenylketonuria | n2=en:faecaluria | rel=r_associated | relid=0 | w=29
  97. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:genetic disorder
    n1=en:classical phenylketonuria | n2=en:genetic disorder | rel=r_associated | relid=0 | w=29
  98. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:glucose-6-phosphate dehydrogenase deficiency anemia
    n1=en:classical phenylketonuria | n2=en:glucose-6-phosphate dehydrogenase deficiency anemia | rel=r_associated | relid=0 | w=29
  99. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:glycogen storage disease type x
    n1=en:classical phenylketonuria | n2=en:glycogen storage disease type x | rel=r_associated | relid=0 | w=29
  100. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:hereditary adrenal unresponsiveness to corticotropin
    n1=en:classical phenylketonuria | n2=en:hereditary adrenal unresponsiveness to corticotropin | rel=r_associated | relid=0 | w=29
  101. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:hereditary factor xi deficiency disease
    n1=en:classical phenylketonuria | n2=en:hereditary factor xi deficiency disease | rel=r_associated | relid=0 | w=29
  102. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:hereditary palmoplantar keratoderma gamborg nielsen type
    n1=en:classical phenylketonuria | n2=en:hereditary palmoplantar keratoderma gamborg nielsen type | rel=r_associated | relid=0 | w=29
  103. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:hnsha due to diphosphoglycerate mutase deficiency
    n1=en:classical phenylketonuria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29
  104. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:hyperkaliuria
    n1=en:classical phenylketonuria | n2=en:hyperkaliuria | rel=r_associated | relid=0 | w=29
  105. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:infantile hypophosphatasia
    n1=en:classical phenylketonuria | n2=en:infantile hypophosphatasia | rel=r_associated | relid=0 | w=29
  106. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:isolated hyperchlorhidrosis
    n1=en:classical phenylketonuria | n2=en:isolated hyperchlorhidrosis | rel=r_associated | relid=0 | w=29
  107. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:lipid metabolism, inborn errors
    n1=en:classical phenylketonuria | n2=en:lipid metabolism, inborn errors | rel=r_associated | relid=0 | w=29
  108. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:marfanoid mental retardation syndrome
    n1=en:classical phenylketonuria | n2=en:marfanoid mental retardation syndrome | rel=r_associated | relid=0 | w=29
  109. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:megalencephalic leukoencephalopathy with subcortical cysts
    n1=en:classical phenylketonuria | n2=en:megalencephalic leukoencephalopathy with subcortical cysts | rel=r_associated | relid=0 | w=29
  110. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:methionine adenosyltransferase deficiency
    n1=en:classical phenylketonuria | n2=en:methionine adenosyltransferase deficiency | rel=r_associated | relid=0 | w=29
  111. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:mild mental retardation
    n1=en:classical phenylketonuria | n2=en:mild mental retardation | rel=r_associated | relid=0 | w=29
  112. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:muscle l-lactate dehydrogenase deficiency
    n1=en:classical phenylketonuria | n2=en:muscle l-lactate dehydrogenase deficiency | rel=r_associated | relid=0 | w=29
  113. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:naxos disease
    n1=en:classical phenylketonuria | n2=en:naxos disease | rel=r_associated | relid=0 | w=29
  114. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:neonatal progeroid syndrome
    n1=en:classical phenylketonuria | n2=en:neonatal progeroid syndrome | rel=r_associated | relid=0 | w=29
  115. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:neural tube defect
    n1=en:classical phenylketonuria | n2=en:neural tube defect | rel=r_associated | relid=0 | w=29
  116. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:oroticaciduria congenital
    n1=en:classical phenylketonuria | n2=en:oroticaciduria congenital | rel=r_associated | relid=0 | w=29
  117. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:other congenital malformations of digestive system
    n1=en:classical phenylketonuria | n2=en:other congenital malformations of digestive system | rel=r_associated | relid=0 | w=29
  118. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:prolonged electroretinal response suppression
    n1=en:classical phenylketonuria | n2=en:prolonged electroretinal response suppression | rel=r_associated | relid=0 | w=29
  119. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:retinitis punctata albescens (disorder)
    n1=en:classical phenylketonuria | n2=en:retinitis punctata albescens (disorder) | rel=r_associated | relid=0 | w=29
  120. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
    n1=en:classical phenylketonuria | n2=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | rel=r_associated | relid=0 | w=29
  121. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:sinus histiocytosis with massive lymphadenopathy
    n1=en:classical phenylketonuria | n2=en:sinus histiocytosis with massive lymphadenopathy | rel=r_associated | relid=0 | w=29
  122. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:sly syndrome
    n1=en:classical phenylketonuria | n2=en:sly syndrome | rel=r_associated | relid=0 | w=29
  123. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:smith-mccort dysplasia
    n1=en:classical phenylketonuria | n2=en:smith-mccort dysplasia | rel=r_associated | relid=0 | w=29
  124. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:spinocerebellar ataxia, autosomal recessive 2
    n1=en:classical phenylketonuria | n2=en:spinocerebellar ataxia, autosomal recessive 2 | rel=r_associated | relid=0 | w=29
  125. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:thoracoschisis
    n1=en:classical phenylketonuria | n2=en:thoracoschisis | rel=r_associated | relid=0 | w=29
  126. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> en:xanthinuria, type i
    n1=en:classical phenylketonuria | n2=en:xanthinuria, type i | rel=r_associated | relid=0 | w=29
  127. en:classical phenylketonuria -- r_associated #0: 29 / 0.674 -> phénylcétonurie classique
    n1=en:classical phenylketonuria | n2=phénylcétonurie classique | rel=r_associated | relid=0 | w=29
  128. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:abnormal fetal duplication
    n1=en:classical phenylketonuria | n2=en:abnormal fetal duplication | rel=r_associated | relid=0 | w=28
  129. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:acid phosphatase deficiency
    n1=en:classical phenylketonuria | n2=en:acid phosphatase deficiency | rel=r_associated | relid=0 | w=28
  130. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:acrocallosal syndrome
    n1=en:classical phenylketonuria | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=28
  131. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:amelogenesis imperfecta - recessive - rough
    n1=en:classical phenylketonuria | n2=en:amelogenesis imperfecta - recessive - rough | rel=r_associated | relid=0 | w=28
  132. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:arterial tortuosity syndrome
    n1=en:classical phenylketonuria | n2=en:arterial tortuosity syndrome | rel=r_associated | relid=0 | w=28
  133. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:atrial septal defect
    n1=en:classical phenylketonuria | n2=en:atrial septal defect | rel=r_associated | relid=0 | w=28
  134. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:autosomal recessive ocular albinism
    n1=en:classical phenylketonuria | n2=en:autosomal recessive ocular albinism | rel=r_associated | relid=0 | w=28
  135. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:autosomal recessive scid
    n1=en:classical phenylketonuria | n2=en:autosomal recessive scid | rel=r_associated | relid=0 | w=28
  136. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:bardet-biedl syndrome
    n1=en:classical phenylketonuria | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=28
  137. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:behr syndrome
    n1=en:classical phenylketonuria | n2=en:behr syndrome | rel=r_associated | relid=0 | w=28
  138. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:borderline mental retardation (i.q. 70-85)
    n1=en:classical phenylketonuria | n2=en:borderline mental retardation (i.q. 70-85) | rel=r_associated | relid=0 | w=28
  139. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:bulbus cordis anomalies and anomalies of cardiac septal closure
    n1=en:classical phenylketonuria | n2=en:bulbus cordis anomalies and anomalies of cardiac septal closure | rel=r_associated | relid=0 | w=28
  140. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:congenital anomaly of neck
    n1=en:classical phenylketonuria | n2=en:congenital anomaly of neck | rel=r_associated | relid=0 | w=28
  141. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:congenital bowing of long bone
    n1=en:classical phenylketonuria | n2=en:congenital bowing of long bone | rel=r_associated | relid=0 | w=28
  142. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:congenital deformity of ankle joint
    n1=en:classical phenylketonuria | n2=en:congenital deformity of ankle joint | rel=r_associated | relid=0 | w=28
  143. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:congenital dysplasia
    n1=en:classical phenylketonuria | n2=en:congenital dysplasia | rel=r_associated | relid=0 | w=28
  144. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:congenital hyperflexion of limb
    n1=en:classical phenylketonuria | n2=en:congenital hyperflexion of limb | rel=r_associated | relid=0 | w=28
  145. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:congenital transferrin deficiency
    n1=en:classical phenylketonuria | n2=en:congenital transferrin deficiency | rel=r_associated | relid=0 | w=28
  146. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:cystathionine beta-synthase deficiency disease
    n1=en:classical phenylketonuria | n2=en:cystathionine beta-synthase deficiency disease | rel=r_associated | relid=0 | w=28
  147. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:de barsy syndrome
    n1=en:classical phenylketonuria | n2=en:de barsy syndrome | rel=r_associated | relid=0 | w=28
  148. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:deafness, sensorineural, and male infertility
    n1=en:classical phenylketonuria | n2=en:deafness, sensorineural, and male infertility | rel=r_associated | relid=0 | w=28
  149. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:epidermolysis bullosa simplex with pyloric atresia
    n1=en:classical phenylketonuria | n2=en:epidermolysis bullosa simplex with pyloric atresia | rel=r_associated | relid=0 | w=28
  150. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:familial hypoaldosteronism
    n1=en:classical phenylketonuria | n2=en:familial hypoaldosteronism | rel=r_associated | relid=0 | w=28
  151. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:fanconi syndrome
    n1=en:classical phenylketonuria | n2=en:fanconi syndrome | rel=r_associated | relid=0 | w=28
  152. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:fatty acid hydroxylase-associated neurodegeneration
    n1=en:classical phenylketonuria | n2=en:fatty acid hydroxylase-associated neurodegeneration | rel=r_associated | relid=0 | w=28
  153. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:fever
    n1=en:classical phenylketonuria | n2=en:fever | rel=r_associated | relid=0 | w=28
  154. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:glutamate formiminotransferase deficiency
    n1=en:classical phenylketonuria | n2=en:glutamate formiminotransferase deficiency | rel=r_associated | relid=0 | w=28
  155. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:harrod doman keele syndrome
    n1=en:classical phenylketonuria | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  156. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:hyperlysinemia
    n1=en:classical phenylketonuria | n2=en:hyperlysinemia | rel=r_associated | relid=0 | w=28
  157. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:knobloch syndrome
    n1=en:classical phenylketonuria | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=28
  158. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:lactase deficiency, congenital
    n1=en:classical phenylketonuria | n2=en:lactase deficiency, congenital | rel=r_associated | relid=0 | w=28
  159. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:mental retardation, x-linked
    n1=en:classical phenylketonuria | n2=en:mental retardation, x-linked | rel=r_associated | relid=0 | w=28
  160. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:mental retardation, x-linked, snyder-robinson type
    n1=en:classical phenylketonuria | n2=en:mental retardation, x-linked, snyder-robinson type | rel=r_associated | relid=0 | w=28
  161. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:methylmalonic aciduria
    n1=en:classical phenylketonuria | n2=en:methylmalonic aciduria | rel=r_associated | relid=0 | w=28
  162. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:morm syndrome
    n1=en:classical phenylketonuria | n2=en:morm syndrome | rel=r_associated | relid=0 | w=28
  163. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:neurodegeneration due to cerebral folate transport deficiency
    n1=en:classical phenylketonuria | n2=en:neurodegeneration due to cerebral folate transport deficiency | rel=r_associated | relid=0 | w=28
  164. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:other congenital anomalies of limbs
    n1=en:classical phenylketonuria | n2=en:other congenital anomalies of limbs | rel=r_associated | relid=0 | w=28
  165. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:pancreatic triacylglycerol lipase deficiency
    n1=en:classical phenylketonuria | n2=en:pancreatic triacylglycerol lipase deficiency | rel=r_associated | relid=0 | w=28
  166. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:persistent cloaca
    n1=en:classical phenylketonuria | n2=en:persistent cloaca | rel=r_associated | relid=0 | w=28
  167. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:phenylketonuria
    n1=en:classical phenylketonuria | n2=en:phenylketonuria | rel=r_associated | relid=0 | w=28
  168. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
    n1=en:classical phenylketonuria | n2=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | rel=r_associated | relid=0 | w=28
  169. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:pseudocholinesterase deficiency
    n1=en:classical phenylketonuria | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=28
  170. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:renpenning syndrome 1
    n1=en:classical phenylketonuria | n2=en:renpenning syndrome 1 | rel=r_associated | relid=0 | w=28
  171. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:spondylo-ocular syndrome
    n1=en:classical phenylketonuria | n2=en:spondylo-ocular syndrome | rel=r_associated | relid=0 | w=28
  172. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:unspecified mental retardation; other impairments of behaviour
    n1=en:classical phenylketonuria | n2=en:unspecified mental retardation; other impairments of behaviour | rel=r_associated | relid=0 | w=28
  173. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour
    n1=en:classical phenylketonuria | n2=en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour | rel=r_associated | relid=0 | w=28
  174. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> en:walker-warburg syndrome
    n1=en:classical phenylketonuria | n2=en:walker-warburg syndrome | rel=r_associated | relid=0 | w=28
  175. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> fièvre
    (médecine)
    n1=en:classical phenylketonuria | n2=fièvre
    (médecine)
    | rel=r_associated | relid=0 | w=28
  176. en:classical phenylketonuria -- r_associated #0: 28 / 0.651 -> phénylcétonurie
    n1=en:classical phenylketonuria | n2=phénylcétonurie | rel=r_associated | relid=0 | w=28
  177. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> anomalie héréditaire
    n1=en:classical phenylketonuria | n2=anomalie héréditaire | rel=r_associated | relid=0 | w=27
  178. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:21-hydroxylase deficiency
    n1=en:classical phenylketonuria | n2=en:21-hydroxylase deficiency | rel=r_associated | relid=0 | w=27
  179. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:amelogenesis imperfecta and gingival hyperplasia syndrome
    n1=en:classical phenylketonuria | n2=en:amelogenesis imperfecta and gingival hyperplasia syndrome | rel=r_associated | relid=0 | w=27
  180. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:biliuria
    n1=en:classical phenylketonuria | n2=en:biliuria | rel=r_associated | relid=0 | w=27
  181. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:carbamoyl-phosphate synthetase i deficiency
    n1=en:classical phenylketonuria | n2=en:carbamoyl-phosphate synthetase i deficiency | rel=r_associated | relid=0 | w=27
  182. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:cerebrotendinous xanthomatosis
    n1=en:classical phenylketonuria | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=27
  183. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:childhood hypophosphatasia (disorder)
    n1=en:classical phenylketonuria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  184. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:childhood myocerebrohepatopathy spectrum
    n1=en:classical phenylketonuria | n2=en:childhood myocerebrohepatopathy spectrum | rel=r_associated | relid=0 | w=27
  185. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:chylomicron retention disease
    n1=en:classical phenylketonuria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  186. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:congenital dyserythropoietic anemia, type ii
    n1=en:classical phenylketonuria | n2=en:congenital dyserythropoietic anemia, type ii | rel=r_associated | relid=0 | w=27
  187. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:congenital functional anomaly
    n1=en:classical phenylketonuria | n2=en:congenital functional anomaly | rel=r_associated | relid=0 | w=27
  188. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:congenital genitourinary abnormality
    n1=en:classical phenylketonuria | n2=en:congenital genitourinary abnormality | rel=r_associated | relid=0 | w=27
  189. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:congenital leptin deficiency
    n1=en:classical phenylketonuria | n2=en:congenital leptin deficiency | rel=r_associated | relid=0 | w=27
  190. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:congenital malposition
    n1=en:classical phenylketonuria | n2=en:congenital malposition | rel=r_associated | relid=0 | w=27
  191. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:congenital pancreatic enterokinase deficiency
    n1=en:classical phenylketonuria | n2=en:congenital pancreatic enterokinase deficiency | rel=r_associated | relid=0 | w=27
  192. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:cutis laxa, autosomal recessive
    n1=en:classical phenylketonuria | n2=en:cutis laxa, autosomal recessive | rel=r_associated | relid=0 | w=27
  193. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:geroderma osteodysplastica
    n1=en:classical phenylketonuria | n2=en:geroderma osteodysplastica | rel=r_associated | relid=0 | w=27
  194. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:glucose-6-phosphate dehydrogenase deficiency
    n1=en:classical phenylketonuria | n2=en:glucose-6-phosphate dehydrogenase deficiency | rel=r_associated | relid=0 | w=27
  195. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:glutamate-cysteine ligase deficiency
    n1=en:classical phenylketonuria | n2=en:glutamate-cysteine ligase deficiency | rel=r_associated | relid=0 | w=27
  196. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:glutathione s-transferase deficiency
    n1=en:classical phenylketonuria | n2=en:glutathione s-transferase deficiency | rel=r_associated | relid=0 | w=27
  197. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:hnsha due to glutathione reductase deficiency
    n1=en:classical phenylketonuria | n2=en:hnsha due to glutathione reductase deficiency | rel=r_associated | relid=0 | w=27
  198. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:kuskokwim disease
    n1=en:classical phenylketonuria | n2=en:kuskokwim disease | rel=r_associated | relid=0 | w=27
  199. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:lethal congenital contracture syndrome 1
    n1=en:classical phenylketonuria | n2=en:lethal congenital contracture syndrome 1 | rel=r_associated | relid=0 | w=27
  200. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:loin pain-hematuria syndrome
    n1=en:classical phenylketonuria | n2=en:loin pain-hematuria syndrome | rel=r_associated | relid=0 | w=27
  201. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:march hemoglobinuria
    n1=en:classical phenylketonuria | n2=en:march hemoglobinuria | rel=r_associated | relid=0 | w=27
  202. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:marles greenberg persaud syndrome
    n1=en:classical phenylketonuria | n2=en:marles greenberg persaud syndrome | rel=r_associated | relid=0 | w=27
  203. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency
    n1=en:classical phenylketonuria | n2=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | rel=r_associated | relid=0 | w=27
  204. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:muscle amp deaminase deficiency
    n1=en:classical phenylketonuria | n2=en:muscle amp deaminase deficiency | rel=r_associated | relid=0 | w=27
  205. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:neonatal jaundice
    n1=en:classical phenylketonuria | n2=en:neonatal jaundice | rel=r_associated | relid=0 | w=27
  206. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:oculocutaneous albinism type 4
    n1=en:classical phenylketonuria | n2=en:oculocutaneous albinism type 4 | rel=r_associated | relid=0 | w=27
  207. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:odontogenic cyst
    n1=en:classical phenylketonuria | n2=en:odontogenic cyst | rel=r_associated | relid=0 | w=27
  208. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:other and unspecified congenital anomalies
    n1=en:classical phenylketonuria | n2=en:other and unspecified congenital anomalies | rel=r_associated | relid=0 | w=27
  209. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:peeling skin syndrome, acral type
    n1=en:classical phenylketonuria | n2=en:peeling skin syndrome, acral type | rel=r_associated | relid=0 | w=27
  210. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:presentey anomaly
    n1=en:classical phenylketonuria | n2=en:presentey anomaly | rel=r_associated | relid=0 | w=27
  211. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:rapadilino syndrome
    n1=en:classical phenylketonuria | n2=en:rapadilino syndrome | rel=r_associated | relid=0 | w=27
  212. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:rhinocephaly
    n1=en:classical phenylketonuria | n2=en:rhinocephaly | rel=r_associated | relid=0 | w=27
  213. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:spondyloenchondrodysplasia with immune dysregulation
    n1=en:classical phenylketonuria | n2=en:spondyloenchondrodysplasia with immune dysregulation | rel=r_associated | relid=0 | w=27
  214. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:succinic semialdehyde dehydrogenase deficiency
    n1=en:classical phenylketonuria | n2=en:succinic semialdehyde dehydrogenase deficiency | rel=r_associated | relid=0 | w=27
  215. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:tetrahydrobiopterin synthesis defect
    n1=en:classical phenylketonuria | n2=en:tetrahydrobiopterin synthesis defect | rel=r_associated | relid=0 | w=27
  216. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:thyroid dyshormonogenesis 4
    n1=en:classical phenylketonuria | n2=en:thyroid dyshormonogenesis 4 | rel=r_associated | relid=0 | w=27
  217. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:unspecified mental retardation; without mention of impairment of behaviour
    n1=en:classical phenylketonuria | n2=en:unspecified mental retardation; without mention of impairment of behaviour | rel=r_associated | relid=0 | w=27
  218. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:waardenburg anophthalmia syndrome
    n1=en:classical phenylketonuria | n2=en:waardenburg anophthalmia syndrome | rel=r_associated | relid=0 | w=27
  219. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> en:wolf-hirschhorn syndrome
    n1=en:classical phenylketonuria | n2=en:wolf-hirschhorn syndrome | rel=r_associated | relid=0 | w=27
  220. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> hyperthermie
    n1=en:classical phenylketonuria | n2=hyperthermie | rel=r_associated | relid=0 | w=27
  221. en:classical phenylketonuria -- r_associated #0: 27 / 0.628 -> maladie de fölling
    n1=en:classical phenylketonuria | n2=maladie de fölling | rel=r_associated | relid=0 | w=27
  222. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> déficit en phénylalanine hydroxylase
    n1=en:classical phenylketonuria | n2=déficit en phénylalanine hydroxylase | rel=r_associated | relid=0 | w=26
  223. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:abnormal urine odor
    n1=en:classical phenylketonuria | n2=en:abnormal urine odor | rel=r_associated | relid=0 | w=26
  224. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:acquired aminoaciduria
    n1=en:classical phenylketonuria | n2=en:acquired aminoaciduria | rel=r_associated | relid=0 | w=26
  225. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:agenesis
    n1=en:classical phenylketonuria | n2=en:agenesis | rel=r_associated | relid=0 | w=26
  226. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:aicardi syndrome
    n1=en:classical phenylketonuria | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=26
  227. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:anemia, hypochromic microcytic, with iron overload
    n1=en:classical phenylketonuria | n2=en:anemia, hypochromic microcytic, with iron overload | rel=r_associated | relid=0 | w=26
  228. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:ataxia telangiectasia syndrome
    n1=en:classical phenylketonuria | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=26
  229. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
    n1=en:classical phenylketonuria | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=26
  230. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:cask related intellectual disability
    n1=en:classical phenylketonuria | n2=en:cask related intellectual disability | rel=r_associated | relid=0 | w=26
  231. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
    n1=en:classical phenylketonuria | n2=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | rel=r_associated | relid=0 | w=26
  232. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:citrin deficiency
    n1=en:classical phenylketonuria | n2=en:citrin deficiency | rel=r_associated | relid=0 | w=26
  233. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:cleft jaw
    n1=en:classical phenylketonuria | n2=en:cleft jaw | rel=r_associated | relid=0 | w=26
  234. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:combined malonic and methylmalonic aciduria
    n1=en:classical phenylketonuria | n2=en:combined malonic and methylmalonic aciduria | rel=r_associated | relid=0 | w=26
  235. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:congenital disorder of glycosylation type ig
    n1=en:classical phenylketonuria | n2=en:congenital disorder of glycosylation type ig | rel=r_associated | relid=0 | w=26
  236. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:congenital dyserythropoietic anemia, type i
    n1=en:classical phenylketonuria | n2=en:congenital dyserythropoietic anemia, type i | rel=r_associated | relid=0 | w=26
  237. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:donnai-barrow syndrome
    n1=en:classical phenylketonuria | n2=en:donnai-barrow syndrome | rel=r_associated | relid=0 | w=26
  238. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:dyskeratosis congenita, autosomal recessive
    n1=en:classical phenylketonuria | n2=en:dyskeratosis congenita, autosomal recessive | rel=r_associated | relid=0 | w=26
  239. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:fraxe intellectual disability syndrome
    n1=en:classical phenylketonuria | n2=en:fraxe intellectual disability syndrome | rel=r_associated | relid=0 | w=26
  240. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:fucosidosis
    n1=en:classical phenylketonuria | n2=en:fucosidosis | rel=r_associated | relid=0 | w=26
  241. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:hmg-coa lyase deficiency
    n1=en:classical phenylketonuria | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=26
  242. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:huntington's disease
    n1=en:classical phenylketonuria | n2=en:huntington's disease | rel=r_associated | relid=0 | w=26
  243. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:hyperornithinemia
    n1=en:classical phenylketonuria | n2=en:hyperornithinemia | rel=r_associated | relid=0 | w=26
  244. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:hyperphenylalaninemia, bh4-deficient, b
    n1=en:classical phenylketonuria | n2=en:hyperphenylalaninemia, bh4-deficient, b | rel=r_associated | relid=0 | w=26
  245. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:hypophosphatasia
    n1=en:classical phenylketonuria | n2=en:hypophosphatasia | rel=r_associated | relid=0 | w=26
  246. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:infantile globoid cell leukodystrophy
    n1=en:classical phenylketonuria | n2=en:infantile globoid cell leukodystrophy | rel=r_associated | relid=0 | w=26
  247. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:interleukin-1 receptor-associated kinase 4 deficiency
    n1=en:classical phenylketonuria | n2=en:interleukin-1 receptor-associated kinase 4 deficiency | rel=r_associated | relid=0 | w=26
  248. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:isolated hypoplasia of the right ventricle
    n1=en:classical phenylketonuria | n2=en:isolated hypoplasia of the right ventricle | rel=r_associated | relid=0 | w=26
  249. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:jankovic rivera syndrome
    n1=en:classical phenylketonuria | n2=en:jankovic rivera syndrome | rel=r_associated | relid=0 | w=26
  250. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:kohlschutter tonz syndrome
    n1=en:classical phenylketonuria | n2=en:kohlschutter tonz syndrome | rel=r_associated | relid=0 | w=26
  251. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:lipid metabolism disorder
    n1=en:classical phenylketonuria | n2=en:lipid metabolism disorder | rel=r_associated | relid=0 | w=26
  252. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:mcdonough syndrome
    n1=en:classical phenylketonuria | n2=en:mcdonough syndrome | rel=r_associated | relid=0 | w=26
  253. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:microcephaly cervical spine fusion anomalies
    n1=en:classical phenylketonuria | n2=en:microcephaly cervical spine fusion anomalies | rel=r_associated | relid=0 | w=26
  254. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:microcephaly deafness syndrome
    n1=en:classical phenylketonuria | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=26
  255. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:microphthalmia, syndromic 4 (disorder)
    n1=en:classical phenylketonuria | n2=en:microphthalmia, syndromic 4 (disorder) | rel=r_associated | relid=0 | w=26
  256. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:neuraminidase deficiency
    n1=en:classical phenylketonuria | n2=en:neuraminidase deficiency | rel=r_associated | relid=0 | w=26
  257. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:pediatric terminology
    n1=en:classical phenylketonuria | n2=en:pediatric terminology | rel=r_associated | relid=0 | w=26
  258. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:porphyruria
    n1=en:classical phenylketonuria | n2=en:porphyruria | rel=r_associated | relid=0 | w=26
  259. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:premature aging syndrome
    n1=en:classical phenylketonuria | n2=en:premature aging syndrome | rel=r_associated | relid=0 | w=26
  260. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:pseudotrisomy 13 syndrome
    n1=en:classical phenylketonuria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  261. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88
    n1=en:classical phenylketonuria | n2=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | rel=r_associated | relid=0 | w=26
  262. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:pyruvate kinase deficiency
    n1=en:classical phenylketonuria | n2=en:pyruvate kinase deficiency | rel=r_associated | relid=0 | w=26
  263. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:sanfilippo syndrome
    n1=en:classical phenylketonuria | n2=en:sanfilippo syndrome | rel=r_associated | relid=0 | w=26
  264. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:sarcosinemia
    n1=en:classical phenylketonuria | n2=en:sarcosinemia | rel=r_associated | relid=0 | w=26
  265. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:savant syndrome
    n1=en:classical phenylketonuria | n2=en:savant syndrome | rel=r_associated | relid=0 | w=26
  266. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:sonoda syndrome
    n1=en:classical phenylketonuria | n2=en:sonoda syndrome | rel=r_associated | relid=0 | w=26
  267. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:syndrome of apparent mineralocorticoid excess
    n1=en:classical phenylketonuria | n2=en:syndrome of apparent mineralocorticoid excess | rel=r_associated | relid=0 | w=26
  268. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:thoracogastroschisis
    n1=en:classical phenylketonuria | n2=en:thoracogastroschisis | rel=r_associated | relid=0 | w=26
  269. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:upper limb defect with eye and ear abnormalities syndrome
    n1=en:classical phenylketonuria | n2=en:upper limb defect with eye and ear abnormalities syndrome | rel=r_associated | relid=0 | w=26
  270. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> en:werdnig-hoffmann disease
    n1=en:classical phenylketonuria | n2=en:werdnig-hoffmann disease | rel=r_associated | relid=0 | w=26
  271. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> maladie héréditaire
    n1=en:classical phenylketonuria | n2=maladie héréditaire | rel=r_associated | relid=0 | w=26
  272. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> pcu
    n1=en:classical phenylketonuria | n2=pcu | rel=r_associated | relid=0 | w=26
  273. en:classical phenylketonuria -- r_associated #0: 26 / 0.605 -> syndrome de Walker-Warburg
    n1=en:classical phenylketonuria | n2=syndrome de Walker-Warburg | rel=r_associated | relid=0 | w=26
  274. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:amegakaryocytic thrombocytopenia with congenital malformation
    n1=en:classical phenylketonuria | n2=en:amegakaryocytic thrombocytopenia with congenital malformation | rel=r_associated | relid=0 | w=25
  275. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:aminomethyltransferase deficiency
    n1=en:classical phenylketonuria | n2=en:aminomethyltransferase deficiency | rel=r_associated | relid=0 | w=25
  276. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:atrophoderma vermiculatum
    n1=en:classical phenylketonuria | n2=en:atrophoderma vermiculatum | rel=r_associated | relid=0 | w=25
  277. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:autosomal recessive spastic paraplegia type 11
    n1=en:classical phenylketonuria | n2=en:autosomal recessive spastic paraplegia type 11 | rel=r_associated | relid=0 | w=25
  278. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:behrens baumann dust syndrome
    n1=en:classical phenylketonuria | n2=en:behrens baumann dust syndrome | rel=r_associated | relid=0 | w=25
  279. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:bietti crystalline corneoretinal dystrophy
    n1=en:classical phenylketonuria | n2=en:bietti crystalline corneoretinal dystrophy | rel=r_associated | relid=0 | w=25
  280. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:classical
    n1=en:classical phenylketonuria | n2=en:classical | rel=r_associated | relid=0 | w=25
  281. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:congenital anomaly of body wall
    n1=en:classical phenylketonuria | n2=en:congenital anomaly of body wall | rel=r_associated | relid=0 | w=25
  282. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism
    n1=en:classical phenylketonuria | n2=en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism | rel=r_associated | relid=0 | w=25
  283. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:deafness, congenital, with inner ear agenesis, microtia, and microdontia
    n1=en:classical phenylketonuria | n2=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | rel=r_associated | relid=0 | w=25
  284. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:developmental malformation of branchial arch
    n1=en:classical phenylketonuria | n2=en:developmental malformation of branchial arch | rel=r_associated | relid=0 | w=25
  285. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:dubin-johnson syndrome
    n1=en:classical phenylketonuria | n2=en:dubin-johnson syndrome | rel=r_associated | relid=0 | w=25
  286. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:factor v and factor viii, combined deficiency of
    n1=en:classical phenylketonuria | n2=en:factor v and factor viii, combined deficiency of | rel=r_associated | relid=0 | w=25
  287. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:funguria
    n1=en:classical phenylketonuria | n2=en:funguria | rel=r_associated | relid=0 | w=25
  288. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:glycine encephalopathy
    n1=en:classical phenylketonuria | n2=en:glycine encephalopathy | rel=r_associated | relid=0 | w=25
  289. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:haematinuria
    n1=en:classical phenylketonuria | n2=en:haematinuria | rel=r_associated | relid=0 | w=25
  290. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:hnsha due to glutathione synthetase deficiency
    n1=en:classical phenylketonuria | n2=en:hnsha due to glutathione synthetase deficiency | rel=r_associated | relid=0 | w=25
  291. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:hyperimmunoglobulin e syndrome
    n1=en:classical phenylketonuria | n2=en:hyperimmunoglobulin e syndrome | rel=r_associated | relid=0 | w=25
  292. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:hyperlipidemia
    n1=en:classical phenylketonuria | n2=en:hyperlipidemia | rel=r_associated | relid=0 | w=25
  293. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:hypertrophy of clitoris
    n1=en:classical phenylketonuria | n2=en:hypertrophy of clitoris | rel=r_associated | relid=0 | w=25
  294. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:hypokalemia, familial
    n1=en:classical phenylketonuria | n2=en:hypokalemia, familial | rel=r_associated | relid=0 | w=25
  295. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:karandikar maria kamble syndrome
    n1=en:classical phenylketonuria | n2=en:karandikar maria kamble syndrome | rel=r_associated | relid=0 | w=25
  296. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:lethal congenital contracture syndrome type 3
    n1=en:classical phenylketonuria | n2=en:lethal congenital contracture syndrome type 3 | rel=r_associated | relid=0 | w=25
  297. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:lissencephaly syndrome, norman-roberts type
    n1=en:classical phenylketonuria | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=25
  298. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:microalbuminuria
    n1=en:classical phenylketonuria | n2=en:microalbuminuria | rel=r_associated | relid=0 | w=25
  299. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:netherton syndrome
    n1=en:classical phenylketonuria | n2=en:netherton syndrome | rel=r_associated | relid=0 | w=25
  300. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:neurodegeneration with brain iron accumulation 4
    n1=en:classical phenylketonuria | n2=en:neurodegeneration with brain iron accumulation 4 | rel=r_associated | relid=0 | w=25
  301. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:nicolaides baraitser syndrome
    n1=en:classical phenylketonuria | n2=en:nicolaides baraitser syndrome | rel=r_associated | relid=0 | w=25
  302. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:odontohypophosphatasia (disorder)
    n1=en:classical phenylketonuria | n2=en:odontohypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25
  303. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:otoonychoperoneal syndrome
    n1=en:classical phenylketonuria | n2=en:otoonychoperoneal syndrome | rel=r_associated | relid=0 | w=25
  304. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:paroxysmal nocturnal hemoglobinuria
    n1=en:classical phenylketonuria | n2=en:paroxysmal nocturnal hemoglobinuria | rel=r_associated | relid=0 | w=25
  305. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:pelizaeus merzbacher like disease
    n1=en:classical phenylketonuria | n2=en:pelizaeus merzbacher like disease | rel=r_associated | relid=0 | w=25
  306. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:persistent mullerian duct syndrome
    n1=en:classical phenylketonuria | n2=en:persistent mullerian duct syndrome | rel=r_associated | relid=0 | w=25
  307. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:prader-willi habitus, osteopenia, and camptodactyly
    n1=en:classical phenylketonuria | n2=en:prader-willi habitus, osteopenia, and camptodactyly | rel=r_associated | relid=0 | w=25
  308. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:pseudohypoaldosteronism, type 1, recessive form
    n1=en:classical phenylketonuria | n2=en:pseudohypoaldosteronism, type 1, recessive form | rel=r_associated | relid=0 | w=25
  309. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:pyuria
    n1=en:classical phenylketonuria | n2=en:pyuria | rel=r_associated | relid=0 | w=25
  310. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:severe mental retardation (i.q. 20-34)
    n1=en:classical phenylketonuria | n2=en:severe mental retardation (i.q. 20-34) | rel=r_associated | relid=0 | w=25
  311. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:spastic paraplegia 15, autosomal recessive
    n1=en:classical phenylketonuria | n2=en:spastic paraplegia 15, autosomal recessive | rel=r_associated | relid=0 | w=25
  312. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:spondylocarpotarsal synostosis syndrome
    n1=en:classical phenylketonuria | n2=en:spondylocarpotarsal synostosis syndrome | rel=r_associated | relid=0 | w=25
  313. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:transient hyperphenylalaninemia
    n1=en:classical phenylketonuria | n2=en:transient hyperphenylalaninemia | rel=r_associated | relid=0 | w=25
  314. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:trisomy 10p
    n1=en:classical phenylketonuria | n2=en:trisomy 10p | rel=r_associated | relid=0 | w=25
  315. en:classical phenylketonuria -- r_associated #0: 25 / 0.581 -> en:valinemia
    n1=en:classical phenylketonuria | n2=en:valinemia | rel=r_associated | relid=0 | w=25
  316. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:3-methylglutaconic aciduria type 1
    n1=en:classical phenylketonuria | n2=en:3-methylglutaconic aciduria type 1 | rel=r_associated | relid=0 | w=24
  317. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:3-methylglutaconic aciduria type 5
    n1=en:classical phenylketonuria | n2=en:3-methylglutaconic aciduria type 5 | rel=r_associated | relid=0 | w=24
  318. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:allgrove syndrome
    n1=en:classical phenylketonuria | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=24
  319. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:antley-bixler syndrome, autosomal dominant
    n1=en:classical phenylketonuria | n2=en:antley-bixler syndrome, autosomal dominant | rel=r_associated | relid=0 | w=24
  320. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:autosomal recessive muscular dystrophy with limb girdle distribution
    n1=en:classical phenylketonuria | n2=en:autosomal recessive muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=24
  321. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:autosomal recessive sideroblastic anemia
    n1=en:classical phenylketonuria | n2=en:autosomal recessive sideroblastic anemia | rel=r_associated | relid=0 | w=24
  322. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:bacteriuria in pregnancy
    n1=en:classical phenylketonuria | n2=en:bacteriuria in pregnancy | rel=r_associated | relid=0 | w=24
  323. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:bilirubinuria
    n1=en:classical phenylketonuria | n2=en:bilirubinuria | rel=r_associated | relid=0 | w=24
  324. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:borjeson-forssman-lehmann syndrome
    n1=en:classical phenylketonuria | n2=en:borjeson-forssman-lehmann syndrome | rel=r_associated | relid=0 | w=24
  325. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:bothnia retinal dystrophy
    n1=en:classical phenylketonuria | n2=en:bothnia retinal dystrophy | rel=r_associated | relid=0 | w=24
  326. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:bowen-conradi syndrome
    n1=en:classical phenylketonuria | n2=en:bowen-conradi syndrome | rel=r_associated | relid=0 | w=24
  327. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:charcot-marie-tooth disease type 4
    n1=en:classical phenylketonuria | n2=en:charcot-marie-tooth disease type 4 | rel=r_associated | relid=0 | w=24
  328. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:chromosome disorder
    n1=en:classical phenylketonuria | n2=en:chromosome disorder | rel=r_associated | relid=0 | w=24
  329. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:cleft lip/palate-ectodermal dysplasia syndrome
    n1=en:classical phenylketonuria | n2=en:cleft lip/palate-ectodermal dysplasia syndrome | rel=r_associated | relid=0 | w=24
  330. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:congenital deformity of hip
    n1=en:classical phenylketonuria | n2=en:congenital deformity of hip | rel=r_associated | relid=0 | w=24
  331. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:congenital disorder of glycosylation type ic
    n1=en:classical phenylketonuria | n2=en:congenital disorder of glycosylation type ic | rel=r_associated | relid=0 | w=24
  332. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:congenital sucrase-isomaltase deficiency
    n1=en:classical phenylketonuria | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=24
  333. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:corpus callosum agenesis neuronopathy
    n1=en:classical phenylketonuria | n2=en:corpus callosum agenesis neuronopathy | rel=r_associated | relid=0 | w=24
  334. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:craniodiaphyseal dysplasia
    n1=en:classical phenylketonuria | n2=en:craniodiaphyseal dysplasia | rel=r_associated | relid=0 | w=24
  335. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:fibular hypoplasia and complex brachydactyly
    n1=en:classical phenylketonuria | n2=en:fibular hypoplasia and complex brachydactyly | rel=r_associated | relid=0 | w=24
  336. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:fronto-facio-nasal dysplasia
    n1=en:classical phenylketonuria | n2=en:fronto-facio-nasal dysplasia | rel=r_associated | relid=0 | w=24
  337. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:fryns macrocephaly
    n1=en:classical phenylketonuria | n2=en:fryns macrocephaly | rel=r_associated | relid=0 | w=24
  338. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:globulinuria
    n1=en:classical phenylketonuria | n2=en:globulinuria | rel=r_associated | relid=0 | w=24
  339. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:glycine dehydrogenase (decarboxylating) deficiency
    n1=en:classical phenylketonuria | n2=en:glycine dehydrogenase (decarboxylating) deficiency | rel=r_associated | relid=0 | w=24
  340. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:hemolytic anemia due to pyruvate kinase deficiency
    n1=en:classical phenylketonuria | n2=en:hemolytic anemia due to pyruvate kinase deficiency | rel=r_associated | relid=0 | w=24
  341. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:hnsha due to pyrimidine-5'-nucleotidase deficiency
    n1=en:classical phenylketonuria | n2=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | rel=r_associated | relid=0 | w=24
  342. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:hypercalciuria
    n1=en:classical phenylketonuria | n2=en:hypercalciuria | rel=r_associated | relid=0 | w=24
  343. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:hyperphosphaturia
    n1=en:classical phenylketonuria | n2=en:hyperphosphaturia | rel=r_associated | relid=0 | w=24
  344. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:hypomagnesemia 1, intestinal
    n1=en:classical phenylketonuria | n2=en:hypomagnesemia 1, intestinal | rel=r_associated | relid=0 | w=24
  345. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:hypophosphatemic rickets with hypercalciuria, hereditary
    n1=en:classical phenylketonuria | n2=en:hypophosphatemic rickets with hypercalciuria, hereditary | rel=r_associated | relid=0 | w=24
  346. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:i-cell disease
    n1=en:classical phenylketonuria | n2=en:i-cell disease | rel=r_associated | relid=0 | w=24
  347. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:jervell and lange nielsen syndrome
    n1=en:classical phenylketonuria | n2=en:jervell and lange nielsen syndrome | rel=r_associated | relid=0 | w=24
  348. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:kabuki syndrome
    n1=en:classical phenylketonuria | n2=en:kabuki syndrome | rel=r_associated | relid=0 | w=24
  349. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:kbg syndrome
    n1=en:classical phenylketonuria | n2=en:kbg syndrome | rel=r_associated | relid=0 | w=24
  350. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:laron syndrome
    n1=en:classical phenylketonuria | n2=en:laron syndrome | rel=r_associated | relid=0 | w=24
  351. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:maroteaux-lamy syndrome
    n1=en:classical phenylketonuria | n2=en:maroteaux-lamy syndrome | rel=r_associated | relid=0 | w=24
  352. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:methylmalonyl-coenzyme a mutase deficiency
    n1=en:classical phenylketonuria | n2=en:methylmalonyl-coenzyme a mutase deficiency | rel=r_associated | relid=0 | w=24
  353. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:morquio syndrome
    n1=en:classical phenylketonuria | n2=en:morquio syndrome | rel=r_associated | relid=0 | w=24
  354. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:niemann-pick disease
    n1=en:classical phenylketonuria | n2=en:niemann-pick disease | rel=r_associated | relid=0 | w=24
  355. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:nitrituria
    n1=en:classical phenylketonuria | n2=en:nitrituria | rel=r_associated | relid=0 | w=24
  356. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:nonaka myopathy
    n1=en:classical phenylketonuria | n2=en:nonaka myopathy | rel=r_associated | relid=0 | w=24
  357. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:norrie syndrome
    n1=en:classical phenylketonuria | n2=en:norrie syndrome | rel=r_associated | relid=0 | w=24
  358. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:opitz trigonocephaly syndrome
    n1=en:classical phenylketonuria | n2=en:opitz trigonocephaly syndrome | rel=r_associated | relid=0 | w=24
  359. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:papillon-lefevre syndrome
    n1=en:classical phenylketonuria | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=24
  360. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:prader-willi syndrome
    n1=en:classical phenylketonuria | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=24
  361. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:purine-nucleoside phosphorylase deficiency
    n1=en:classical phenylketonuria | n2=en:purine-nucleoside phosphorylase deficiency | rel=r_associated | relid=0 | w=24
  362. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:rna polymerase iii-related leukodystrophy
    n1=en:classical phenylketonuria | n2=en:rna polymerase iii-related leukodystrophy | rel=r_associated | relid=0 | w=24
  363. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:semenuria
    n1=en:classical phenylketonuria | n2=en:semenuria | rel=r_associated | relid=0 | w=24
  364. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:spastic ataxia, charlevoix-saguenay type
    n1=en:classical phenylketonuria | n2=en:spastic ataxia, charlevoix-saguenay type | rel=r_associated | relid=0 | w=24
  365. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:spondyloenchondrodysplasia
    n1=en:classical phenylketonuria | n2=en:spondyloenchondrodysplasia | rel=r_associated | relid=0 | w=24
  366. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:spondyloepiphyseal dysplasia, omani type
    n1=en:classical phenylketonuria | n2=en:spondyloepiphyseal dysplasia, omani type | rel=r_associated | relid=0 | w=24
  367. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:tungland bellman syndrome
    n1=en:classical phenylketonuria | n2=en:tungland bellman syndrome | rel=r_associated | relid=0 | w=24
  368. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:tyrosinemia type ii
    n1=en:classical phenylketonuria | n2=en:tyrosinemia type ii | rel=r_associated | relid=0 | w=24
  369. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:unspecified intellectual disabilities
    n1=en:classical phenylketonuria | n2=en:unspecified intellectual disabilities | rel=r_associated | relid=0 | w=24
  370. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:urine microscopy leukocytes present finding
    n1=en:classical phenylketonuria | n2=en:urine microscopy leukocytes present finding | rel=r_associated | relid=0 | w=24
  371. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:vrozené poruchy metabolismu nec in mdrcze18_1
    n1=en:classical phenylketonuria | n2=en:vrozené poruchy metabolismu nec in mdrcze18_1 | rel=r_associated | relid=0 | w=24
  372. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:waisman syndrome
    n1=en:classical phenylketonuria | n2=en:waisman syndrome | rel=r_associated | relid=0 | w=24
  373. en:classical phenylketonuria -- r_associated #0: 24 / 0.558 -> en:warsaw breakage syndrome
    n1=en:classical phenylketonuria | n2=en:warsaw breakage syndrome | rel=r_associated | relid=0 | w=24
  374. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:abnormal urine
    n1=en:classical phenylketonuria | n2=en:abnormal urine | rel=r_associated | relid=0 | w=23
  375. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:acephalostomia
    n1=en:classical phenylketonuria | n2=en:acephalostomia | rel=r_associated | relid=0 | w=23
  376. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:ammoniuria
    n1=en:classical phenylketonuria | n2=en:ammoniuria | rel=r_associated | relid=0 | w=23
  377. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:argininosuccinic aciduria
    n1=en:classical phenylketonuria | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=23
  378. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:cerebellar ataxia, cayman type
    n1=en:classical phenylketonuria | n2=en:cerebellar ataxia, cayman type | rel=r_associated | relid=0 | w=23
  379. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:chondrodysplasia punctata syndrome
    n1=en:classical phenylketonuria | n2=en:chondrodysplasia punctata syndrome | rel=r_associated | relid=0 | w=23
  380. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:congenital anomaly of back
    n1=en:classical phenylketonuria | n2=en:congenital anomaly of back | rel=r_associated | relid=0 | w=23
  381. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:congenital anomaly of the hematopoietic system
    n1=en:classical phenylketonuria | n2=en:congenital anomaly of the hematopoietic system | rel=r_associated | relid=0 | w=23
  382. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:congenital cataracts, facial dysmorphism, and neuropathy
    n1=en:classical phenylketonuria | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=23
  383. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:congenital deformity of knee joint
    n1=en:classical phenylketonuria | n2=en:congenital deformity of knee joint | rel=r_associated | relid=0 | w=23
  384. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:congenital deformity of scapula
    n1=en:classical phenylketonuria | n2=en:congenital deformity of scapula | rel=r_associated | relid=0 | w=23
  385. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:congenital disorder of glycosylation type ia
    n1=en:classical phenylketonuria | n2=en:congenital disorder of glycosylation type ia | rel=r_associated | relid=0 | w=23
  386. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:congenital malformation of genital organs
    n1=en:classical phenylketonuria | n2=en:congenital malformation of genital organs | rel=r_associated | relid=0 | w=23
  387. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:congenital plasminogen activator inhibitor deficiency type 1
    n1=en:classical phenylketonuria | n2=en:congenital plasminogen activator inhibitor deficiency type 1 | rel=r_associated | relid=0 | w=23
  388. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:congenital urinary system abnormality
    n1=en:classical phenylketonuria | n2=en:congenital urinary system abnormality | rel=r_associated | relid=0 | w=23
  389. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:diabetes mellitus
    n1=en:classical phenylketonuria | n2=en:diabetes mellitus | rel=r_associated | relid=0 | w=23
  390. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome
    n1=en:classical phenylketonuria | n2=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | rel=r_associated | relid=0 | w=23
  391. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:ectodermal dysplasia/ skin fragility syndrome
    n1=en:classical phenylketonuria | n2=en:ectodermal dysplasia/ skin fragility syndrome | rel=r_associated | relid=0 | w=23
  392. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:ectromelia
    n1=en:classical phenylketonuria | n2=en:ectromelia | rel=r_associated | relid=0 | w=23
  393. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:female restricted epilepsy with intellectual disability syndrome
    n1=en:classical phenylketonuria | n2=en:female restricted epilepsy with intellectual disability syndrome | rel=r_associated | relid=0 | w=23
  394. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:fetal postural deformity
    n1=en:classical phenylketonuria | n2=en:fetal postural deformity | rel=r_associated | relid=0 | w=23
  395. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:goniodysgenesis-mental retardation-short stature syndrome
    n1=en:classical phenylketonuria | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=23
  396. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:heart malformation
    n1=en:classical phenylketonuria | n2=en:heart malformation | rel=r_associated | relid=0 | w=23
  397. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:hypermanganesemia with dystonia polycythemia and cirrhosis
    n1=en:classical phenylketonuria | n2=en:hypermanganesemia with dystonia polycythemia and cirrhosis | rel=r_associated | relid=0 | w=23
  398. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:hyperphosphatasia with mental retardation
    n1=en:classical phenylketonuria | n2=en:hyperphosphatasia with mental retardation | rel=r_associated | relid=0 | w=23
  399. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:hypospadias-mental retardation syndrome
    n1=en:classical phenylketonuria | n2=en:hypospadias-mental retardation syndrome | rel=r_associated | relid=0 | w=23
  400. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:imperforate anus
    n1=en:classical phenylketonuria | n2=en:imperforate anus | rel=r_associated | relid=0 | w=23
  401. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:laryngeal atresia
    n1=en:classical phenylketonuria | n2=en:laryngeal atresia | rel=r_associated | relid=0 | w=23
  402. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:lubs x-linked mental retardation syndrome
    n1=en:classical phenylketonuria | n2=en:lubs x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=23
  403. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:macular corneal dystrophy
    n1=en:classical phenylketonuria | n2=en:macular corneal dystrophy | rel=r_associated | relid=0 | w=23
  404. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:masa syndrome (disorder)
    n1=en:classical phenylketonuria | n2=en:masa syndrome (disorder) | rel=r_associated | relid=0 | w=23
  405. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:microcephalic primordial dwarfism toriello type
    n1=en:classical phenylketonuria | n2=en:microcephalic primordial dwarfism toriello type | rel=r_associated | relid=0 | w=23
  406. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:miller-mckusick-malvaux-syndrome (3m syndrome)
    n1=en:classical phenylketonuria | n2=en:miller-mckusick-malvaux-syndrome (3m syndrome) | rel=r_associated | relid=0 | w=23
  407. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:multicentric osteolysis nodulosis arthropathy spectrum
    n1=en:classical phenylketonuria | n2=en:multicentric osteolysis nodulosis arthropathy spectrum | rel=r_associated | relid=0 | w=23
  408. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:myopathy, early-onset, with fatal cardiomyopathy
    n1=en:classical phenylketonuria | n2=en:myopathy, early-onset, with fatal cardiomyopathy | rel=r_associated | relid=0 | w=23
  409. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:nutritional mental retardation
    n1=en:classical phenylketonuria | n2=en:nutritional mental retardation | rel=r_associated | relid=0 | w=23
  410. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:phenylketonuria ii
    n1=en:classical phenylketonuria | n2=en:phenylketonuria ii | rel=r_associated | relid=0 | w=23
  411. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:polyuria
    n1=en:classical phenylketonuria | n2=en:polyuria | rel=r_associated | relid=0 | w=23
  412. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:renal tubulopathy with encephalopathy and liver failure syndrome
    n1=en:classical phenylketonuria | n2=en:renal tubulopathy with encephalopathy and liver failure syndrome | rel=r_associated | relid=0 | w=23
  413. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:rett syndrome
    n1=en:classical phenylketonuria | n2=en:rett syndrome | rel=r_associated | relid=0 | w=23
  414. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:sirenomelia
    n1=en:classical phenylketonuria | n2=en:sirenomelia | rel=r_associated | relid=0 | w=23
  415. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:sitosterolemia with xanthomatosis
    n1=en:classical phenylketonuria | n2=en:sitosterolemia with xanthomatosis | rel=r_associated | relid=0 | w=23
  416. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:spondyloepiphyseal dysplasia tarda, toledo type
    n1=en:classical phenylketonuria | n2=en:spondyloepiphyseal dysplasia tarda, toledo type | rel=r_associated | relid=0 | w=23
  417. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:sudden infant death with dysgenesis of the testes syndrome
    n1=en:classical phenylketonuria | n2=en:sudden infant death with dysgenesis of the testes syndrome | rel=r_associated | relid=0 | w=23
  418. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:transcobalamin ii deficiency
    n1=en:classical phenylketonuria | n2=en:transcobalamin ii deficiency | rel=r_associated | relid=0 | w=23
  419. en:classical phenylketonuria -- r_associated #0: 23 / 0.535 -> en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment
    n1=en:classical phenylketonuria | n2=en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment | rel=r_associated | relid=0 | w=23
  420. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> eczéma
    n1=en:classical phenylketonuria | n2=eczéma | rel=r_associated | relid=0 | w=22
  421. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:3-methylglutaconic aciduria type iv
    n1=en:classical phenylketonuria | n2=en:3-methylglutaconic aciduria type iv | rel=r_associated | relid=0 | w=22
  422. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:5 alpha steroid reductase 2 deficiency
    n1=en:classical phenylketonuria | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=22
  423. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:acrodermatitis enteropathica
    n1=en:classical phenylketonuria | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=22
  424. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:arginine:glycine amidinotransferase deficiency
    n1=en:classical phenylketonuria | n2=en:arginine:glycine amidinotransferase deficiency | rel=r_associated | relid=0 | w=22
  425. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:ataxia with vitamin e deficiency
    n1=en:classical phenylketonuria | n2=en:ataxia with vitamin e deficiency | rel=r_associated | relid=0 | w=22
  426. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:autosomal recessive distal osteolysis syndrome
    n1=en:classical phenylketonuria | n2=en:autosomal recessive distal osteolysis syndrome | rel=r_associated | relid=0 | w=22
  427. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:autosomal recessive idiopathic familial dystonia
    n1=en:classical phenylketonuria | n2=en:autosomal recessive idiopathic familial dystonia | rel=r_associated | relid=0 | w=22
  428. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:autosomal recessive primary microcephaly
    n1=en:classical phenylketonuria | n2=en:autosomal recessive primary microcephaly | rel=r_associated | relid=0 | w=22
  429. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:brown-vialetto-van laere syndrome
    n1=en:classical phenylketonuria | n2=en:brown-vialetto-van laere syndrome | rel=r_associated | relid=0 | w=22
  430. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:candiduria
    n1=en:classical phenylketonuria | n2=en:candiduria | rel=r_associated | relid=0 | w=22
  431. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:cebocephaly
    n1=en:classical phenylketonuria | n2=en:cebocephaly | rel=r_associated | relid=0 | w=22
  432. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:cerebroretinal microangiopathy with calcifications and cysts (disorder)
    n1=en:classical phenylketonuria | n2=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | rel=r_associated | relid=0 | w=22
  433. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism
    n1=en:classical phenylketonuria | n2=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=22
  434. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:coffin-siris syndrome
    n1=en:classical phenylketonuria | n2=en:coffin-siris syndrome | rel=r_associated | relid=0 | w=22
  435. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:congenital amegakaryocytic thrombocytopenia
    n1=en:classical phenylketonuria | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=22
  436. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:congenital anomaly of visual system
    n1=en:classical phenylketonuria | n2=en:congenital anomaly of visual system | rel=r_associated | relid=0 | w=22
  437. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:congenital deformity of mitral valve annulus
    n1=en:classical phenylketonuria | n2=en:congenital deformity of mitral valve annulus | rel=r_associated | relid=0 | w=22
  438. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:congenital flat back deformity
    n1=en:classical phenylketonuria | n2=en:congenital flat back deformity | rel=r_associated | relid=0 | w=22
  439. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:congenital foot deformity
    n1=en:classical phenylketonuria | n2=en:congenital foot deformity | rel=r_associated | relid=0 | w=22
  440. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
    n1=en:classical phenylketonuria | n2=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | rel=r_associated | relid=0 | w=22
  441. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:congenital musculoskeletal defect
    n1=en:classical phenylketonuria | n2=en:congenital musculoskeletal defect | rel=r_associated | relid=0 | w=22
  442. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:congenital stenosis
    n1=en:classical phenylketonuria | n2=en:congenital stenosis | rel=r_associated | relid=0 | w=22
  443. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:cryptophthalmos syndrome
    n1=en:classical phenylketonuria | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=22
  444. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:de sanctis-cacchione syndrome
    n1=en:classical phenylketonuria | n2=en:de sanctis-cacchione syndrome | rel=r_associated | relid=0 | w=22
  445. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:deafness, progressive, with stapes fixation
    n1=en:classical phenylketonuria | n2=en:deafness, progressive, with stapes fixation | rel=r_associated | relid=0 | w=22
  446. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:deficiency of glucosyltransferase 1
    n1=en:classical phenylketonuria | n2=en:deficiency of glucosyltransferase 1 | rel=r_associated | relid=0 | w=22
  447. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:digeorge syndrome
    n1=en:classical phenylketonuria | n2=en:digeorge syndrome | rel=r_associated | relid=0 | w=22
  448. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:encephalopathy due to sulfite oxidase deficiency
    n1=en:classical phenylketonuria | n2=en:encephalopathy due to sulfite oxidase deficiency | rel=r_associated | relid=0 | w=22
  449. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:familial c3b inhibitor deficiency syndrome
    n1=en:classical phenylketonuria | n2=en:familial c3b inhibitor deficiency syndrome | rel=r_associated | relid=0 | w=22
  450. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:hereditary factor x deficiency disease
    n1=en:classical phenylketonuria | n2=en:hereditary factor x deficiency disease | rel=r_associated | relid=0 | w=22
  451. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:hereditary factor xii deficiency disease
    n1=en:classical phenylketonuria | n2=en:hereditary factor xii deficiency disease | rel=r_associated | relid=0 | w=22
  452. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:hereditary fructose intolerance
    n1=en:classical phenylketonuria | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=22
  453. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:hnsha due to aldolase a deficiency
    n1=en:classical phenylketonuria | n2=en:hnsha due to aldolase a deficiency | rel=r_associated | relid=0 | w=22
  454. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:hnsha due to nadh diaphorase deficiency
    n1=en:classical phenylketonuria | n2=en:hnsha due to nadh diaphorase deficiency | rel=r_associated | relid=0 | w=22
  455. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:hypermagnesuria
    n1=en:classical phenylketonuria | n2=en:hypermagnesuria | rel=r_associated | relid=0 | w=22
  456. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:hypermethioniuria
    n1=en:classical phenylketonuria | n2=en:hypermethioniuria | rel=r_associated | relid=0 | w=22
  457. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:hyponatriuria
    n1=en:classical phenylketonuria | n2=en:hyponatriuria | rel=r_associated | relid=0 | w=22
  458. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:isosthenuria
    n1=en:classical phenylketonuria | n2=en:isosthenuria | rel=r_associated | relid=0 | w=22
  459. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:lethal congenital contracture syndrome 2
    n1=en:classical phenylketonuria | n2=en:lethal congenital contracture syndrome 2 | rel=r_associated | relid=0 | w=22
  460. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:leukotriene c4 synthase deficiency
    n1=en:classical phenylketonuria | n2=en:leukotriene c4 synthase deficiency | rel=r_associated | relid=0 | w=22
  461. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:mannosidosis
    n1=en:classical phenylketonuria | n2=en:mannosidosis | rel=r_associated | relid=0 | w=22
  462. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency
    n1=en:classical phenylketonuria | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | rel=r_associated | relid=0 | w=22
  463. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:mental retardation
    n1=en:classical phenylketonuria | n2=en:mental retardation | rel=r_associated | relid=0 | w=22
  464. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:methylcrotonyl-coa carboxylase deficiency
    n1=en:classical phenylketonuria | n2=en:methylcrotonyl-coa carboxylase deficiency | rel=r_associated | relid=0 | w=22
  465. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:mitochondrial dna depletion syndrome 2 (myopathic type)
    n1=en:classical phenylketonuria | n2=en:mitochondrial dna depletion syndrome 2 (myopathic type) | rel=r_associated | relid=0 | w=22
  466. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome
    n1=en:classical phenylketonuria | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=22
  467. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:neuroacanthocytosis
    n1=en:classical phenylketonuria | n2=en:neuroacanthocytosis | rel=r_associated | relid=0 | w=22
  468. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:northern epilepsy syndrome
    n1=en:classical phenylketonuria | n2=en:northern epilepsy syndrome | rel=r_associated | relid=0 | w=22
  469. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:partington x-linked mental retardation syndrome
    n1=en:classical phenylketonuria | n2=en:partington x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=22
  470. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:perniola krajewska carnevale syndrome
    n1=en:classical phenylketonuria | n2=en:perniola krajewska carnevale syndrome | rel=r_associated | relid=0 | w=22
  471. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:pontocerebellar hypoplasia type 2
    n1=en:classical phenylketonuria | n2=en:pontocerebellar hypoplasia type 2 | rel=r_associated | relid=0 | w=22
  472. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:porphobilinogen synthase deficiency
    n1=en:classical phenylketonuria | n2=en:porphobilinogen synthase deficiency | rel=r_associated | relid=0 | w=22
  473. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:prickle1-related progressive myoclonus epilepsy with ataxia
    n1=en:classical phenylketonuria | n2=en:prickle1-related progressive myoclonus epilepsy with ataxia | rel=r_associated | relid=0 | w=22
  474. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:propionic acidemia
    n1=en:classical phenylketonuria | n2=en:propionic acidemia | rel=r_associated | relid=0 | w=22
  475. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:pterygium colli
    n1=en:classical phenylketonuria | n2=en:pterygium colli | rel=r_associated | relid=0 | w=22
  476. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:purine-pyrimidine metabolism, inborn errors
    n1=en:classical phenylketonuria | n2=en:purine-pyrimidine metabolism, inborn errors | rel=r_associated | relid=0 | w=22
  477. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:reardon hall slaney syndrome
    n1=en:classical phenylketonuria | n2=en:reardon hall slaney syndrome | rel=r_associated | relid=0 | w=22
  478. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:reduced phenylalanine hydroxylase activity
    n1=en:classical phenylketonuria | n2=en:reduced phenylalanine hydroxylase activity | rel=r_associated | relid=0 | w=22
  479. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:spinal muscular atrophy with respiratory distress 1
    n1=en:classical phenylketonuria | n2=en:spinal muscular atrophy with respiratory distress 1 | rel=r_associated | relid=0 | w=22
  480. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:transposition of great vessels
    n1=en:classical phenylketonuria | n2=en:transposition of great vessels | rel=r_associated | relid=0 | w=22
  481. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:tyrosinemia, type iii
    n1=en:classical phenylketonuria | n2=en:tyrosinemia, type iii | rel=r_associated | relid=0 | w=22
  482. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:uv-sensitive syndrome
    n1=en:classical phenylketonuria | n2=en:uv-sensitive syndrome | rel=r_associated | relid=0 | w=22
  483. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:wolman disease
    n1=en:classical phenylketonuria | n2=en:wolman disease | rel=r_associated | relid=0 | w=22
  484. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> en:zellweger syndrome
    n1=en:classical phenylketonuria | n2=en:zellweger syndrome | rel=r_associated | relid=0 | w=22
  485. en:classical phenylketonuria -- r_associated #0: 22 / 0.512 -> malformation cardiaque
    n1=en:classical phenylketonuria | n2=malformation cardiaque | rel=r_associated | relid=0 | w=22
  486. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:2-hydroxyglutaric aciduria
    n1=en:classical phenylketonuria | n2=en:2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=21
  487. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:adenine phosphoribosyltransferase deficiency
    n1=en:classical phenylketonuria | n2=en:adenine phosphoribosyltransferase deficiency | rel=r_associated | relid=0 | w=21
  488. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:adenylosuccinate lyase deficiency (disorder)
    n1=en:classical phenylketonuria | n2=en:adenylosuccinate lyase deficiency (disorder) | rel=r_associated | relid=0 | w=21
  489. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:al awadi syndrome
    n1=en:classical phenylketonuria | n2=en:al awadi syndrome | rel=r_associated | relid=0 | w=21
  490. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:aminoacylase 1 deficiency
    n1=en:classical phenylketonuria | n2=en:aminoacylase 1 deficiency | rel=r_associated | relid=0 | w=21
  491. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:arthrogryposis multiplex congenita, neurogenic type (disorder)
    n1=en:classical phenylketonuria | n2=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | rel=r_associated | relid=0 | w=21
  492. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:ateliotic dwarfism without insulinopenia
    n1=en:classical phenylketonuria | n2=en:ateliotic dwarfism without insulinopenia | rel=r_associated | relid=0 | w=21
  493. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:cheilognathopalatoschisis
    n1=en:classical phenylketonuria | n2=en:cheilognathopalatoschisis | rel=r_associated | relid=0 | w=21
  494. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:congenital eye disorder
    n1=en:classical phenylketonuria | n2=en:congenital eye disorder | rel=r_associated | relid=0 | w=21
  495. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:congenital hallux valgus
    n1=en:classical phenylketonuria | n2=en:congenital hallux valgus | rel=r_associated | relid=0 | w=21
  496. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:congenital red cell hypoplasia
    n1=en:classical phenylketonuria | n2=en:congenital red cell hypoplasia | rel=r_associated | relid=0 | w=21
  497. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:disorder characterized by fever
    n1=en:classical phenylketonuria | n2=en:disorder characterized by fever | rel=r_associated | relid=0 | w=21
  498. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:disorder of glycosaminoglycan metabolism
    n1=en:classical phenylketonuria | n2=en:disorder of glycosaminoglycan metabolism | rel=r_associated | relid=0 | w=21
  499. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:ehlers-danlos syndrome, type vi
    n1=en:classical phenylketonuria | n2=en:ehlers-danlos syndrome, type vi | rel=r_associated | relid=0 | w=21
  500. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:familial erythrocytosis due to diphosphoglycerate mutase deficiency
    n1=en:classical phenylketonuria | n2=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=21
  501. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:fatal infantile lactic acidosis with methylmalonic aciduria
    n1=en:classical phenylketonuria | n2=en:fatal infantile lactic acidosis with methylmalonic aciduria | rel=r_associated | relid=0 | w=21
  502. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:folinic acid responsive seizure syndrome
    n1=en:classical phenylketonuria | n2=en:folinic acid responsive seizure syndrome | rel=r_associated | relid=0 | w=21
  503. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:gamma-glutamyltransferase deficiency
    n1=en:classical phenylketonuria | n2=en:gamma-glutamyltransferase deficiency | rel=r_associated | relid=0 | w=21
  504. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:gaze palsy, familial horizontal, with progressive scoliosis
    n1=en:classical phenylketonuria | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=21
  505. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:gurrieri sammito bellussi syndrome
    n1=en:classical phenylketonuria | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=21
  506. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:hereditary methemoglobinemia, enzymatic type
    n1=en:classical phenylketonuria | n2=en:hereditary methemoglobinemia, enzymatic type | rel=r_associated | relid=0 | w=21
  507. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:hereditary spastic paralysis, infantile onset ascending
    n1=en:classical phenylketonuria | n2=en:hereditary spastic paralysis, infantile onset ascending | rel=r_associated | relid=0 | w=21
  508. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:hydroxykynureninuria
    n1=en:classical phenylketonuria | n2=en:hydroxykynureninuria | rel=r_associated | relid=0 | w=21
  509. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:hyperprolinemia type 1
    n1=en:classical phenylketonuria | n2=en:hyperprolinemia type 1 | rel=r_associated | relid=0 | w=21
  510. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:hyperprolinemia type 2
    n1=en:classical phenylketonuria | n2=en:hyperprolinemia type 2 | rel=r_associated | relid=0 | w=21
  511. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:hypomyelination and congenital cataract
    n1=en:classical phenylketonuria | n2=en:hypomyelination and congenital cataract | rel=r_associated | relid=0 | w=21
  512. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:inborn errors of metabolism nec in cst95
    n1=en:classical phenylketonuria | n2=en:inborn errors of metabolism nec in cst95 | rel=r_associated | relid=0 | w=21
  513. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:inherited disorder of thyroid metabolism
    n1=en:classical phenylketonuria | n2=en:inherited disorder of thyroid metabolism | rel=r_associated | relid=0 | w=21
  514. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:isaacs syndrome
    n1=en:classical phenylketonuria | n2=en:isaacs syndrome | rel=r_associated | relid=0 | w=21
  515. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:klinefelter syndrome
    n1=en:classical phenylketonuria | n2=en:klinefelter syndrome | rel=r_associated | relid=0 | w=21
  516. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
    n1=en:classical phenylketonuria | n2=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | rel=r_associated | relid=0 | w=21
  517. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:lujan fryns syndrome
    n1=en:classical phenylketonuria | n2=en:lujan fryns syndrome | rel=r_associated | relid=0 | w=21
  518. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:majeed syndrome
    n1=en:classical phenylketonuria | n2=en:majeed syndrome | rel=r_associated | relid=0 | w=21
  519. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:methylene thf reductase deficiency and homocystinuria
    n1=en:classical phenylketonuria | n2=en:methylene thf reductase deficiency and homocystinuria | rel=r_associated | relid=0 | w=21
  520. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:microcephaly-capillary malformation syndrome
    n1=en:classical phenylketonuria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  521. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:microcephaly, amish type (disorder)
    n1=en:classical phenylketonuria | n2=en:microcephaly, amish type (disorder) | rel=r_associated | relid=0 | w=21
  522. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:mucopolysaccharidosis type i
    n1=en:classical phenylketonuria | n2=en:mucopolysaccharidosis type i | rel=r_associated | relid=0 | w=21
  523. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:multiple sulfatase deficiency disease
    n1=en:classical phenylketonuria | n2=en:multiple sulfatase deficiency disease | rel=r_associated | relid=0 | w=21
  524. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:n-acetylglutamate synthase deficiency
    n1=en:classical phenylketonuria | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=21
  525. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:nathalie syndrome
    n1=en:classical phenylketonuria | n2=en:nathalie syndrome | rel=r_associated | relid=0 | w=21
  526. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:north american indian childhood cirrhosis
    n1=en:classical phenylketonuria | n2=en:north american indian childhood cirrhosis | rel=r_associated | relid=0 | w=21
  527. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:ornithine carbamoyltransferase deficiency disease
    n1=en:classical phenylketonuria | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=21
  528. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:placental steroid sulfatase deficiency
    n1=en:classical phenylketonuria | n2=en:placental steroid sulfatase deficiency | rel=r_associated | relid=0 | w=21
  529. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:pneumatouria
    n1=en:classical phenylketonuria | n2=en:pneumatouria | rel=r_associated | relid=0 | w=21
  530. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:post procedural haematuria
    n1=en:classical phenylketonuria | n2=en:post procedural haematuria | rel=r_associated | relid=0 | w=21
  531. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:precocious puberty
    n1=en:classical phenylketonuria | n2=en:precocious puberty | rel=r_associated | relid=0 | w=21
  532. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:pyruvate carboxylase deficiency
    n1=en:classical phenylketonuria | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=21
  533. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:richards-rundle syndrome
    n1=en:classical phenylketonuria | n2=en:richards-rundle syndrome | rel=r_associated | relid=0 | w=21
  534. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:saito kuba tsuruta syndrome
    n1=en:classical phenylketonuria | n2=en:saito kuba tsuruta syndrome | rel=r_associated | relid=0 | w=21
  535. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:severe early childhood onset retinal dystrophy
    n1=en:classical phenylketonuria | n2=en:severe early childhood onset retinal dystrophy | rel=r_associated | relid=0 | w=21
  536. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:sulfite oxidase deficiency
    n1=en:classical phenylketonuria | n2=en:sulfite oxidase deficiency | rel=r_associated | relid=0 | w=21
  537. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:tay-sachs disease
    n1=en:classical phenylketonuria | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=21
  538. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:tuberous sclerosis
    n1=en:classical phenylketonuria | n2=en:tuberous sclerosis | rel=r_associated | relid=0 | w=21
  539. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:type ii acrocephalopolysyndactyly
    n1=en:classical phenylketonuria | n2=en:type ii acrocephalopolysyndactyly | rel=r_associated | relid=0 | w=21
  540. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:urocanase deficiency
    n1=en:classical phenylketonuria | n2=en:urocanase deficiency | rel=r_associated | relid=0 | w=21
  541. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:ventricular septal defect
    n1=en:classical phenylketonuria | n2=en:ventricular septal defect | rel=r_associated | relid=0 | w=21
  542. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> en:verloes bourguignon syndrome
    n1=en:classical phenylketonuria | n2=en:verloes bourguignon syndrome | rel=r_associated | relid=0 | w=21
  543. en:classical phenylketonuria -- r_associated #0: 21 / 0.488 -> fièvre
    n1=en:classical phenylketonuria | n2=fièvre | rel=r_associated | relid=0 | w=21
  544. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> acidémie glutarique de type 1
    n1=en:classical phenylketonuria | n2=acidémie glutarique de type 1 | rel=r_associated | relid=0 | w=20
  545. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> acido-cétose
    n1=en:classical phenylketonuria | n2=acido-cétose | rel=r_associated | relid=0 | w=20
  546. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> acidocétose
    n1=en:classical phenylketonuria | n2=acidocétose | rel=r_associated | relid=0 | w=20
  547. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> acidoses lactiques (classification selon Cohen et Woods)
    n1=en:classical phenylketonuria | n2=acidoses lactiques (classification selon Cohen et Woods) | rel=r_associated | relid=0 | w=20
  548. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> acidurie glutarique de type 1
    n1=en:classical phenylketonuria | n2=acidurie glutarique de type 1 | rel=r_associated | relid=0 | w=20
  549. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> acidurie mévalonique
    n1=en:classical phenylketonuria | n2=acidurie mévalonique | rel=r_associated | relid=0 | w=20
  550. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> acrodermatite entéropathique
    n1=en:classical phenylketonuria | n2=acrodermatite entéropathique | rel=r_associated | relid=0 | w=20
  551. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> adénite sinusale cytophagique
    n1=en:classical phenylketonuria | n2=adénite sinusale cytophagique | rel=r_associated | relid=0 | w=20
  552. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> affection cardiaque
    n1=en:classical phenylketonuria | n2=affection cardiaque | rel=r_associated | relid=0 | w=20
  553. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> affection oculaire congénitale
    n1=en:classical phenylketonuria | n2=affection oculaire congénitale | rel=r_associated | relid=0 | w=20
  554. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> affections cardiaques
    n1=en:classical phenylketonuria | n2=affections cardiaques | rel=r_associated | relid=0 | w=20
  555. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> albinisme
    n1=en:classical phenylketonuria | n2=albinisme | rel=r_associated | relid=0 | w=20
  556. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> ancyloglosse
    n1=en:classical phenylketonuria | n2=ancyloglosse | rel=r_associated | relid=0 | w=20
  557. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> ankyloglosse
    n1=en:classical phenylketonuria | n2=ankyloglosse | rel=r_associated | relid=0 | w=20
  558. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> anomalie cardiaque
    n1=en:classical phenylketonuria | n2=anomalie cardiaque | rel=r_associated | relid=0 | w=20
  559. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> anomalie chromosomique
    n1=en:classical phenylketonuria | n2=anomalie chromosomique | rel=r_associated | relid=0 | w=20
  560. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> anomalie congénitale de l'oeil
    n1=en:classical phenylketonuria | n2=anomalie congénitale de l'oeil | rel=r_associated | relid=0 | w=20
  561. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> anomalie cytogénétique
    n1=en:classical phenylketonuria | n2=anomalie cytogénétique | rel=r_associated | relid=0 | w=20
  562. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> anomalie du coeur
    n1=en:classical phenylketonuria | n2=anomalie du coeur | rel=r_associated | relid=0 | w=20
  563. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> anomalie du développement
    n1=en:classical phenylketonuria | n2=anomalie du développement | rel=r_associated | relid=0 | w=20
  564. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> anomalie du septum auriculaire
    n1=en:classical phenylketonuria | n2=anomalie du septum auriculaire | rel=r_associated | relid=0 | w=20
  565. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> anormalité des chromosomes
    n1=en:classical phenylketonuria | n2=anormalité des chromosomes | rel=r_associated | relid=0 | w=20
  566. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> arriération
    n1=en:classical phenylketonuria | n2=arriération | rel=r_associated | relid=0 | w=20
  567. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> arriération mentale
    n1=en:classical phenylketonuria | n2=arriération mentale | rel=r_associated | relid=0 | w=20
  568. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> atrésie
    n1=en:classical phenylketonuria | n2=atrésie | rel=r_associated | relid=0 | w=20
  569. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> bébé bronzé (syndrome du)
    n1=en:classical phenylketonuria | n2=bébé bronzé (syndrome du) | rel=r_associated | relid=0 | w=20
  570. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> BEC DE LIEVRE
    n1=en:classical phenylketonuria | n2=BEC DE LIEVRE | rel=r_associated | relid=0 | w=20
  571. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Bec de lièvre
    n1=en:classical phenylketonuria | n2=Bec de lièvre | rel=r_associated | relid=0 | w=20
  572. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> bec de lièvre
    n1=en:classical phenylketonuria | n2=bec de lièvre | rel=r_associated | relid=0 | w=20
  573. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> brides amniotiques (syndrome des)
    n1=en:classical phenylketonuria | n2=brides amniotiques (syndrome des) | rel=r_associated | relid=0 | w=20
  574. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> card
    n1=en:classical phenylketonuria | n2=card | rel=r_associated | relid=0 | w=20
  575. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> cardiopathie
    n1=en:classical phenylketonuria | n2=cardiopathie | rel=r_associated | relid=0 | w=20
  576. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> cardiopathies
    n1=en:classical phenylketonuria | n2=cardiopathies | rel=r_associated | relid=0 | w=20
  577. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> cataracte-atrophie du cervelet-myopathie
    n1=en:classical phenylketonuria | n2=cataracte-atrophie du cervelet-myopathie | rel=r_associated | relid=0 | w=20
  578. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> cétoacidose
    n1=en:classical phenylketonuria | n2=cétoacidose | rel=r_associated | relid=0 | w=20
  579. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> cétoacidurie à chaînes ramifiées
    n1=en:classical phenylketonuria | n2=cétoacidurie à chaînes ramifiées | rel=r_associated | relid=0 | w=20
  580. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> cheilo-gnatho-palatoschisis
    n1=en:classical phenylketonuria | n2=cheilo-gnatho-palatoschisis | rel=r_associated | relid=0 | w=20
  581. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> cheilognathopalatoschisis
    n1=en:classical phenylketonuria | n2=cheilognathopalatoschisis | rel=r_associated | relid=0 | w=20
  582. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Chopart (désarticulation de)
    n1=en:classical phenylketonuria | n2=Chopart (désarticulation de) | rel=r_associated | relid=0 | w=20
  583. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Chorée
    n1=en:classical phenylketonuria | n2=Chorée | rel=r_associated | relid=0 | w=20
  584. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> chorée de Huntington
    n1=en:classical phenylketonuria | n2=chorée de Huntington | rel=r_associated | relid=0 | w=20
  585. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> chorée de huntington
    n1=en:classical phenylketonuria | n2=chorée de huntington | rel=r_associated | relid=0 | w=20
  586. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> chorée de saint jean
    n1=en:classical phenylketonuria | n2=chorée de saint jean | rel=r_associated | relid=0 | w=20
  587. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> chorée de Sydenham
    n1=en:classical phenylketonuria | n2=chorée de Sydenham | rel=r_associated | relid=0 | w=20
  588. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> chorée de sydenham
    n1=en:classical phenylketonuria | n2=chorée de sydenham | rel=r_associated | relid=0 | w=20
  589. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> chorée héréditaire
    n1=en:classical phenylketonuria | n2=chorée héréditaire | rel=r_associated | relid=0 | w=20
  590. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> chorée rhumatismale
    n1=en:classical phenylketonuria | n2=chorée rhumatismale | rel=r_associated | relid=0 | w=20
  591. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> chorée rhumatismale sans atteinte cardiaque
    n1=en:classical phenylketonuria | n2=chorée rhumatismale sans atteinte cardiaque | rel=r_associated | relid=0 | w=20
  592. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> chorées
    n1=en:classical phenylketonuria | n2=chorées | rel=r_associated | relid=0 | w=20
  593. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> communication interauriculaire
    n1=en:classical phenylketonuria | n2=communication interauriculaire | rel=r_associated | relid=0 | w=20
  594. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> congénital
    n1=en:classical phenylketonuria | n2=congénital | rel=r_associated | relid=0 | w=20
  595. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> congenital
    n1=en:classical phenylketonuria | n2=congenital | rel=r_associated | relid=0 | w=20
  596. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> congénitale
    n1=en:classical phenylketonuria | n2=congénitale | rel=r_associated | relid=0 | w=20
  597. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> crânio-sténose
    n1=en:classical phenylketonuria | n2=crânio-sténose | rel=r_associated | relid=0 | w=20
  598. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> craniosténose
    n1=en:classical phenylketonuria | n2=craniosténose | rel=r_associated | relid=0 | w=20
  599. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> crâniosténose
    n1=en:classical phenylketonuria | n2=crâniosténose | rel=r_associated | relid=0 | w=20
  600. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> craniosynostose
    n1=en:classical phenylketonuria | n2=craniosynostose | rel=r_associated | relid=0 | w=20
  601. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> crâniosynostose
    n1=en:classical phenylketonuria | n2=crâniosynostose | rel=r_associated | relid=0 | w=20
  602. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> cristallurie
    n1=en:classical phenylketonuria | n2=cristallurie | rel=r_associated | relid=0 | w=20
  603. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> cyclopia
    n1=en:classical phenylketonuria | n2=cyclopia | rel=r_associated | relid=0 | w=20
  604. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> cyclopie
    n1=en:classical phenylketonuria | n2=cyclopie | rel=r_associated | relid=0 | w=20
  605. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> danse de saint Guy
    n1=en:classical phenylketonuria | n2=danse de saint Guy | rel=r_associated | relid=0 | w=20
  606. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> débilité mentale
    n1=en:classical phenylketonuria | n2=débilité mentale | rel=r_associated | relid=0 | w=20
  607. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> déficience congénitale
    n1=en:classical phenylketonuria | n2=déficience congénitale | rel=r_associated | relid=0 | w=20
  608. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> déficience intellectuelle
    n1=en:classical phenylketonuria | n2=déficience intellectuelle | rel=r_associated | relid=0 | w=20
  609. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> déficit congénital en mégacaryocytes
    n1=en:classical phenylketonuria | n2=déficit congénital en mégacaryocytes | rel=r_associated | relid=0 | w=20
  610. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> déficit en céto-acide décarboxylase
    n1=en:classical phenylketonuria | n2=déficit en céto-acide décarboxylase | rel=r_associated | relid=0 | w=20
  611. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> déficit en cytochrome oxydase
    n1=en:classical phenylketonuria | n2=déficit en cytochrome oxydase | rel=r_associated | relid=0 | w=20
  612. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> déficit en cytochrome-c oxydase
    n1=en:classical phenylketonuria | n2=déficit en cytochrome-c oxydase | rel=r_associated | relid=0 | w=20
  613. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> déficit en neuraminidase
    n1=en:classical phenylketonuria | n2=déficit en neuraminidase | rel=r_associated | relid=0 | w=20
  614. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> déficit en prolidase
    n1=en:classical phenylketonuria | n2=déficit en prolidase | rel=r_associated | relid=0 | w=20
  615. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> déficit en pyruvate carboxylase
    n1=en:classical phenylketonuria | n2=déficit en pyruvate carboxylase | rel=r_associated | relid=0 | w=20
  616. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> déficit en semialdéhyde succinique-déshydrogénase
    n1=en:classical phenylketonuria | n2=déficit en semialdéhyde succinique-déshydrogénase | rel=r_associated | relid=0 | w=20
  617. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> déformation congénitale
    n1=en:classical phenylketonuria | n2=déformation congénitale | rel=r_associated | relid=0 | w=20
  618. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> diabète (accidents vasculaires cérébraux du)
    n1=en:classical phenylketonuria | n2=diabète (accidents vasculaires cérébraux du) | rel=r_associated | relid=0 | w=20
  619. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> diabète sucré
    n1=en:classical phenylketonuria | n2=diabète sucré | rel=r_associated | relid=0 | w=20
  620. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> diabète sucré de type 2 avec surdité
    n1=en:classical phenylketonuria | n2=diabète sucré de type 2 avec surdité | rel=r_associated | relid=0 | w=20
  621. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> diabète, photomyoclonies, surdité, néphropathie et dysfonction cérébrale
    n1=en:classical phenylketonuria | n2=diabète, photomyoclonies, surdité, néphropathie et dysfonction cérébrale | rel=r_associated | relid=0 | w=20
  622. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> difformité congénitale
    n1=en:classical phenylketonuria | n2=difformité congénitale | rel=r_associated | relid=0 | w=20
  623. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> division palatine
    n1=en:classical phenylketonuria | n2=division palatine | rel=r_associated | relid=0 | w=20
  624. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> dysplasie craniodiaphysaire
    n1=en:classical phenylketonuria | n2=dysplasie craniodiaphysaire | rel=r_associated | relid=0 | w=20
  625. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> dysplasie ectodermique
    n1=en:classical phenylketonuria | n2=dysplasie ectodermique | rel=r_associated | relid=0 | w=20
  626. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental
    n1=en:classical phenylketonuria | n2=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | rel=r_associated | relid=0 | w=20
  627. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> dysplasie ectodermique, ectrodactylie et dystrophie maculaire
    n1=en:classical phenylketonuria | n2=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | rel=r_associated | relid=0 | w=20
  628. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie)
    n1=en:classical phenylketonuria | n2=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | rel=r_associated | relid=0 | w=20
  629. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> ectopia cordis
    n1=en:classical phenylketonuria | n2=ectopia cordis | rel=r_associated | relid=0 | w=20
  630. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> ectopie cardiaque
    n1=en:classical phenylketonuria | n2=ectopie cardiaque | rel=r_associated | relid=0 | w=20
  631. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> ectromélie
    n1=en:classical phenylketonuria | n2=ectromélie | rel=r_associated | relid=0 | w=20
  632. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> eczema
    n1=en:classical phenylketonuria | n2=eczema | rel=r_associated | relid=0 | w=20
  633. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> élévation de la température corporelle
    n1=en:classical phenylketonuria | n2=élévation de la température corporelle | rel=r_associated | relid=0 | w=20
  634. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> elliptocytose héréditaire
    n1=en:classical phenylketonuria | n2=elliptocytose héréditaire | rel=r_associated | relid=0 | w=20
  635. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:12q14 microdeletion syndrome
    n1=en:classical phenylketonuria | n2=en:12q14 microdeletion syndrome | rel=r_associated | relid=0 | w=20
  636. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:17q11.2 microduplication syndrome
    n1=en:classical phenylketonuria | n2=en:17q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=20
  637. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:1p21.3 microdeletion syndrome
    n1=en:classical phenylketonuria | n2=en:1p21.3 microdeletion syndrome | rel=r_associated | relid=0 | w=20
  638. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:abnormalities, drug-induced
    n1=en:classical phenylketonuria | n2=en:abnormalities, drug-induced | rel=r_associated | relid=0 | w=20
  639. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:abnormality, severe teratoid
    n1=en:classical phenylketonuria | n2=en:abnormality, severe teratoid | rel=r_associated | relid=0 | w=20
  640. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:absent corpus callosum
    n1=en:classical phenylketonuria | n2=en:absent corpus callosum | rel=r_associated | relid=0 | w=20
  641. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:acquired lactase deficiency
    n1=en:classical phenylketonuria | n2=en:acquired lactase deficiency | rel=r_associated | relid=0 | w=20
  642. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:acrorenal mandibular syndrome
    n1=en:classical phenylketonuria | n2=en:acrorenal mandibular syndrome | rel=r_associated | relid=0 | w=20
  643. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein
    n1=en:classical phenylketonuria | n2=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | rel=r_associated | relid=0 | w=20
  644. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:additional sex chromosome
    n1=en:classical phenylketonuria | n2=en:additional sex chromosome | rel=r_associated | relid=0 | w=20
  645. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:adducted thumbs and arthrogryposis syndrome christian type
    n1=en:classical phenylketonuria | n2=en:adducted thumbs and arthrogryposis syndrome christian type | rel=r_associated | relid=0 | w=20
  646. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:adrenal cytomegaly
    n1=en:classical phenylketonuria | n2=en:adrenal cytomegaly | rel=r_associated | relid=0 | w=20
  647. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:adult hypophosphatasia (disorder)
    n1=en:classical phenylketonuria | n2=en:adult hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=20
  648. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
    n1=en:classical phenylketonuria | n2=en:agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome | rel=r_associated | relid=0 | w=20
  649. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:albinism
    n1=en:classical phenylketonuria | n2=en:albinism | rel=r_associated | relid=0 | w=20
  650. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:alkaptonuria
    n1=en:classical phenylketonuria | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=20
  651. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:amino acid deficiency
    n1=en:classical phenylketonuria | n2=en:amino acid deficiency | rel=r_associated | relid=0 | w=20
  652. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:amino acid transport disorder
    n1=en:classical phenylketonuria | n2=en:amino acid transport disorder | rel=r_associated | relid=0 | w=20
  653. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:amino acid transport disorders, inborn
    n1=en:classical phenylketonuria | n2=en:amino acid transport disorders, inborn | rel=r_associated | relid=0 | w=20
  654. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:amniotic band syndrome
    n1=en:classical phenylketonuria | n2=en:amniotic band syndrome | rel=r_associated | relid=0 | w=20
  655. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:anal imperforation
    n1=en:classical phenylketonuria | n2=en:anal imperforation | rel=r_associated | relid=0 | w=20
  656. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:anauxetic dysplasia
    n1=en:classical phenylketonuria | n2=en:anauxetic dysplasia | rel=r_associated | relid=0 | w=20
  657. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:and mental retardation
    n1=en:classical phenylketonuria | n2=en:and mental retardation | rel=r_associated | relid=0 | w=20
  658. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:and microgenitalism
    n1=en:classical phenylketonuria | n2=en:and microgenitalism | rel=r_associated | relid=0 | w=20
  659. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Angelman syndrome
    n1=en:classical phenylketonuria | n2=en:Angelman syndrome | rel=r_associated | relid=0 | w=20
  660. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Angelman's syndrome
    n1=en:classical phenylketonuria | n2=en:Angelman's syndrome | rel=r_associated | relid=0 | w=20
  661. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:aniridia and intellectual disability syndrome
    n1=en:classical phenylketonuria | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=20
  662. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:ankyloglossia
    n1=en:classical phenylketonuria | n2=en:ankyloglossia | rel=r_associated | relid=0 | w=20
  663. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:anterior plagiocephalies, synostotic
    n1=en:classical phenylketonuria | n2=en:anterior plagiocephalies, synostotic | rel=r_associated | relid=0 | w=20
  664. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:anxiety disorder
    n1=en:classical phenylketonuria | n2=en:anxiety disorder | rel=r_associated | relid=0 | w=20
  665. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:aplasia, nos
    n1=en:classical phenylketonuria | n2=en:aplasia, nos | rel=r_associated | relid=0 | w=20
  666. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:arachnodactyly and intellectual disability with facial dysmorphism syndrome
    n1=en:classical phenylketonuria | n2=en:arachnodactyly and intellectual disability with facial dysmorphism syndrome | rel=r_associated | relid=0 | w=20
  667. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:arakawa syndrome ii
    n1=en:classical phenylketonuria | n2=en:arakawa syndrome ii | rel=r_associated | relid=0 | w=20
  668. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:atresia
    n1=en:classical phenylketonuria | n2=en:atresia | rel=r_associated | relid=0 | w=20
  669. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:autosomal recessive inheritance
    n1=en:classical phenylketonuria | n2=en:autosomal recessive inheritance | rel=r_associated | relid=0 | w=20
  670. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:autosomal recessive spastic paraplegia type 39
    n1=en:classical phenylketonuria | n2=en:autosomal recessive spastic paraplegia type 39 | rel=r_associated | relid=0 | w=20
  671. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:bamforth syndrome
    n1=en:classical phenylketonuria | n2=en:bamforth syndrome | rel=r_associated | relid=0 | w=20
  672. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:benign neonatal hyperaminoaciduria
    n1=en:classical phenylketonuria | n2=en:benign neonatal hyperaminoaciduria | rel=r_associated | relid=0 | w=20
  673. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:bestrophinopathy, autosomal recessive
    n1=en:classical phenylketonuria | n2=en:bestrophinopathy, autosomal recessive | rel=r_associated | relid=0 | w=20
  674. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:beta-methylcrotonylglycinuria
    n1=en:classical phenylketonuria | n2=en:beta-methylcrotonylglycinuria | rel=r_associated | relid=0 | w=20
  675. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:biotinidase deficiency
    n1=en:classical phenylketonuria | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=20
  676. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:birth defect
    n1=en:classical phenylketonuria | n2=en:birth defect | rel=r_associated | relid=0 | w=20
  677. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:bisphosphoglycerate mutase deficiency
    n1=en:classical phenylketonuria | n2=en:bisphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=20
  678. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:brachioskeletogenital syndrome
    n1=en:classical phenylketonuria | n2=en:brachioskeletogenital syndrome | rel=r_associated | relid=0 | w=20
  679. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:braddock syndrome
    n1=en:classical phenylketonuria | n2=en:braddock syndrome | rel=r_associated | relid=0 | w=20
  680. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:brain calcification rajab type
    n1=en:classical phenylketonuria | n2=en:brain calcification rajab type | rel=r_associated | relid=0 | w=20
  681. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:brain diseases, metabolic, inborn
    n1=en:classical phenylketonuria | n2=en:brain diseases, metabolic, inborn | rel=r_associated | relid=0 | w=20
  682. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:branched-chain ketoaciduria
    n1=en:classical phenylketonuria | n2=en:branched-chain ketoaciduria | rel=r_associated | relid=0 | w=20
  683. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:butyryl-coa dehydrogenase deficiency
    n1=en:classical phenylketonuria | n2=en:butyryl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
  684. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:card
    n1=en:classical phenylketonuria | n2=en:card | rel=r_associated | relid=0 | w=20
  685. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:cardiac diseases
    n1=en:classical phenylketonuria | n2=en:cardiac diseases | rel=r_associated | relid=0 | w=20
  686. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:caroli disease
    n1=en:classical phenylketonuria | n2=en:caroli disease | rel=r_associated | relid=0 | w=20
  687. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:caudal dysplasia
    n1=en:classical phenylketonuria | n2=en:caudal dysplasia | rel=r_associated | relid=0 | w=20
  688. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:celosomy
    n1=en:classical phenylketonuria | n2=en:celosomy | rel=r_associated | relid=0 | w=20
  689. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:cerebral ventriculomegaly
    n1=en:classical phenylketonuria | n2=en:cerebral ventriculomegaly | rel=r_associated | relid=0 | w=20
  690. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:certain congenital musculoskeletal deformities
    n1=en:classical phenylketonuria | n2=en:certain congenital musculoskeletal deformities | rel=r_associated | relid=0 | w=20
  691. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:cervical hypertrichosis and peripheral neuropathy syndrome
    n1=en:classical phenylketonuria | n2=en:cervical hypertrichosis and peripheral neuropathy syndrome | rel=r_associated | relid=0 | w=20
  692. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:charge syndrome
    n1=en:classical phenylketonuria | n2=en:charge syndrome | rel=r_associated | relid=0 | w=20
  693. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:chromosomal abnormality
    n1=en:classical phenylketonuria | n2=en:chromosomal abnormality | rel=r_associated | relid=0 | w=20
  694. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:circulating enzyme deficiency
    n1=en:classical phenylketonuria | n2=en:circulating enzyme deficiency | rel=r_associated | relid=0 | w=20
  695. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:classical maple syrup urine disease
    n1=en:classical phenylketonuria | n2=en:classical maple syrup urine disease | rel=r_associated | relid=0 | w=20
  696. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:cleft lip and palate
    n1=en:classical phenylketonuria | n2=en:cleft lip and palate | rel=r_associated | relid=0 | w=20
  697. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:cleft maxilla
    n1=en:classical phenylketonuria | n2=en:cleft maxilla | rel=r_associated | relid=0 | w=20
  698. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:cleft palate
    n1=en:classical phenylketonuria | n2=en:cleft palate | rel=r_associated | relid=0 | w=20
  699. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:cleft palate with cleft lip
    n1=en:classical phenylketonuria | n2=en:cleft palate with cleft lip | rel=r_associated | relid=0 | w=20
  700. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:clubfoot
    n1=en:classical phenylketonuria | n2=en:clubfoot | rel=r_associated | relid=0 | w=20
  701. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:complete trisomy 18 syndrome
    n1=en:classical phenylketonuria | n2=en:complete trisomy 18 syndrome | rel=r_associated | relid=0 | w=20
  702. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital abnormal fusion
    n1=en:classical phenylketonuria | n2=en:congenital abnormal fusion | rel=r_associated | relid=0 | w=20
  703. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital analbuminemia
    n1=en:classical phenylketonuria | n2=en:congenital analbuminemia | rel=r_associated | relid=0 | w=20
  704. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital anomaly
    n1=en:classical phenylketonuria | n2=en:congenital anomaly | rel=r_associated | relid=0 | w=20
  705. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital anomaly of face
    n1=en:classical phenylketonuria | n2=en:congenital anomaly of face | rel=r_associated | relid=0 | w=20
  706. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital anomaly of skeletal bone
    n1=en:classical phenylketonuria | n2=en:congenital anomaly of skeletal bone | rel=r_associated | relid=0 | w=20
  707. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital cardiovascular abnormality
    n1=en:classical phenylketonuria | n2=en:congenital cardiovascular abnormality | rel=r_associated | relid=0 | w=20
  708. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital cataract with ataxia and deafness syndrome
    n1=en:classical phenylketonuria | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=20
  709. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital defect
    n1=en:classical phenylketonuria | n2=en:congenital defect | rel=r_associated | relid=0 | w=20
  710. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital deformity of clavicle
    n1=en:classical phenylketonuria | n2=en:congenital deformity of clavicle | rel=r_associated | relid=0 | w=20
  711. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital deformity of pinna
    n1=en:classical phenylketonuria | n2=en:congenital deformity of pinna | rel=r_associated | relid=0 | w=20
  712. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type 1h
    n1=en:classical phenylketonuria | n2=en:congenital disorder of glycosylation type 1h | rel=r_associated | relid=0 | w=20
  713. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type 2e
    n1=en:classical phenylketonuria | n2=en:congenital disorder of glycosylation type 2e | rel=r_associated | relid=0 | w=20
  714. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type id
    n1=en:classical phenylketonuria | n2=en:congenital disorder of glycosylation type id | rel=r_associated | relid=0 | w=20
  715. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type ie
    n1=en:classical phenylketonuria | n2=en:congenital disorder of glycosylation type ie | rel=r_associated | relid=0 | w=20
  716. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation, type if
    n1=en:classical phenylketonuria | n2=en:congenital disorder of glycosylation, type if | rel=r_associated | relid=0 | w=20
  717. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital enlargement
    n1=en:classical phenylketonuria | n2=en:congenital enlargement | rel=r_associated | relid=0 | w=20
  718. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital extension deformity
    n1=en:classical phenylketonuria | n2=en:congenital extension deformity | rel=r_associated | relid=0 | w=20
  719. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital flexion deformity
    n1=en:classical phenylketonuria | n2=en:congenital flexion deformity | rel=r_associated | relid=0 | w=20
  720. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital hand and foot deformity
    n1=en:classical phenylketonuria | n2=en:congenital hand and foot deformity | rel=r_associated | relid=0 | w=20
  721. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital keratoglobus
    n1=en:classical phenylketonuria | n2=en:congenital keratoglobus | rel=r_associated | relid=0 | w=20
  722. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital macrocephaly
    n1=en:classical phenylketonuria | n2=en:congenital macrocephaly | rel=r_associated | relid=0 | w=20
  723. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital malformation
    n1=en:classical phenylketonuria | n2=en:congenital malformation | rel=r_associated | relid=0 | w=20
  724. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital malformation syndrome
    n1=en:classical phenylketonuria | n2=en:congenital malformation syndrome | rel=r_associated | relid=0 | w=20
  725. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital malformation syndrome related to known exogenous cause
    n1=en:classical phenylketonuria | n2=en:congenital malformation syndrome related to known exogenous cause | rel=r_associated | relid=0 | w=20
  726. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital nervous system disorder
    n1=en:classical phenylketonuria | n2=en:congenital nervous system disorder | rel=r_associated | relid=0 | w=20
  727. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital opacity
    n1=en:classical phenylketonuria | n2=en:congenital opacity | rel=r_associated | relid=0 | w=20
  728. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital septation
    n1=en:classical phenylketonuria | n2=en:congenital septation | rel=r_associated | relid=0 | w=20
  729. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital sequestration
    n1=en:classical phenylketonuria | n2=en:congenital sequestration | rel=r_associated | relid=0 | w=20
  730. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital systemic disorder
    n1=en:classical phenylketonuria | n2=en:congenital systemic disorder | rel=r_associated | relid=0 | w=20
  731. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:congenital vena cava abnormality
    n1=en:classical phenylketonuria | n2=en:congenital vena cava abnormality | rel=r_associated | relid=0 | w=20
  732. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:conjoined twins
    n1=en:classical phenylketonuria | n2=en:conjoined twins | rel=r_associated | relid=0 | w=20
  733. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:connatal disorder
    n1=en:classical phenylketonuria | n2=en:connatal disorder | rel=r_associated | relid=0 | w=20
  734. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:cooper jabs syndrome
    n1=en:classical phenylketonuria | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=20
  735. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:craniofacial ulnar renal syndrome
    n1=en:classical phenylketonuria | n2=en:craniofacial ulnar renal syndrome | rel=r_associated | relid=0 | w=20
  736. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:cranioschisis
    n1=en:classical phenylketonuria | n2=en:cranioschisis | rel=r_associated | relid=0 | w=20
  737. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:craniostenosis
    n1=en:classical phenylketonuria | n2=en:craniostenosis | rel=r_associated | relid=0 | w=20
  738. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:craniosynostosis
    n1=en:classical phenylketonuria | n2=en:craniosynostosis | rel=r_associated | relid=0 | w=20
  739. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:cri du chat syndrome
    n1=en:classical phenylketonuria | n2=en:cri du chat syndrome | rel=r_associated | relid=0 | w=20
  740. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:cryptophthalmia
    n1=en:classical phenylketonuria | n2=en:cryptophthalmia | rel=r_associated | relid=0 | w=20
  741. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:cutaneous photosensitivity and lethal colitis syndrome
    n1=en:classical phenylketonuria | n2=en:cutaneous photosensitivity and lethal colitis syndrome | rel=r_associated | relid=0 | w=20
  742. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:cyclopia
    n1=en:classical phenylketonuria | n2=en:cyclopia | rel=r_associated | relid=0 | w=20
  743. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:De Sanctis-Cacchione syndrome
    n1=en:classical phenylketonuria | n2=en:De Sanctis-Cacchione syndrome | rel=r_associated | relid=0 | w=20
  744. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:deafness
    n1=en:classical phenylketonuria | n2=en:deafness | rel=r_associated | relid=0 | w=20
  745. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:deafness and myopia syndrome
    n1=en:classical phenylketonuria | n2=en:deafness and myopia syndrome | rel=r_associated | relid=0 | w=20
  746. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome
    n1=en:classical phenylketonuria | n2=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | rel=r_associated | relid=0 | w=20
  747. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:decreased hdl cholesterol
    n1=en:classical phenylketonuria | n2=en:decreased hdl cholesterol | rel=r_associated | relid=0 | w=20
  748. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:decreased tetrasialotransferrin
    n1=en:classical phenylketonuria | n2=en:decreased tetrasialotransferrin | rel=r_associated | relid=0 | w=20
  749. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:defect in post-translational modification of lysosomal enzymes
    n1=en:classical phenylketonuria | n2=en:defect in post-translational modification of lysosomal enzymes | rel=r_associated | relid=0 | w=20
  750. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:deficiency in enzyme complexes of mitochondrial respiratory chain
    n1=en:classical phenylketonuria | n2=en:deficiency in enzyme complexes of mitochondrial respiratory chain | rel=r_associated | relid=0 | w=20
  751. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:deficiency of steryl-sulfatase
    n1=en:classical phenylketonuria | n2=en:deficiency of steryl-sulfatase | rel=r_associated | relid=0 | w=20
  752. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:dehydration
    n1=en:classical phenylketonuria | n2=en:dehydration | rel=r_associated | relid=0 | w=20
  753. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:delayed epiphyseal fusion
    n1=en:classical phenylketonuria | n2=en:delayed epiphyseal fusion | rel=r_associated | relid=0 | w=20
  754. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
    n1=en:classical phenylketonuria | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=20
  755. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:developmental fault
    n1=en:classical phenylketonuria | n2=en:developmental fault | rel=r_associated | relid=0 | w=20
  756. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:developmental immaturity
    n1=en:classical phenylketonuria | n2=en:developmental immaturity | rel=r_associated | relid=0 | w=20
  757. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:developmental stricture
    n1=en:classical phenylketonuria | n2=en:developmental stricture | rel=r_associated | relid=0 | w=20
  758. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:diaphanospondylodysostosis
    n1=en:classical phenylketonuria | n2=en:diaphanospondylodysostosis | rel=r_associated | relid=0 | w=20
  759. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:dihydropyrimidinase deficiency
    n1=en:classical phenylketonuria | n2=en:dihydropyrimidinase deficiency | rel=r_associated | relid=0 | w=20
  760. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:dihydropyrimidine dehydrogenase deficiency
    n1=en:classical phenylketonuria | n2=en:dihydropyrimidine dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
  761. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:disorder due to cytochrome p450 enzyme variant
    n1=en:classical phenylketonuria | n2=en:disorder due to cytochrome p450 enzyme variant | rel=r_associated | relid=0 | w=20
  762. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:disorder due to n-acetyltransferase enzyme variant
    n1=en:classical phenylketonuria | n2=en:disorder due to n-acetyltransferase enzyme variant | rel=r_associated | relid=0 | w=20
  763. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:disorder of amino acid and organic acid metabolism
    n1=en:classical phenylketonuria | n2=en:disorder of amino acid and organic acid metabolism | rel=r_associated | relid=0 | w=20
  764. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:disorder of branched-chain amino acid metabolism
    n1=en:classical phenylketonuria | n2=en:disorder of branched-chain amino acid metabolism | rel=r_associated | relid=0 | w=20
  765. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:disorder of creatine synthesis
    n1=en:classical phenylketonuria | n2=en:disorder of creatine synthesis | rel=r_associated | relid=0 | w=20
  766. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:disorder of histidine metabolism
    n1=en:classical phenylketonuria | n2=en:disorder of histidine metabolism | rel=r_associated | relid=0 | w=20
  767. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:disorder of lysine and hydroxylysine metabolism
    n1=en:classical phenylketonuria | n2=en:disorder of lysine and hydroxylysine metabolism | rel=r_associated | relid=0 | w=20
  768. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:disorder of pyruvate metabolism and mitochondrial respiratory chain
    n1=en:classical phenylketonuria | n2=en:disorder of pyruvate metabolism and mitochondrial respiratory chain | rel=r_associated | relid=0 | w=20
  769. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:disorder of sialic acid metabolism
    n1=en:classical phenylketonuria | n2=en:disorder of sialic acid metabolism | rel=r_associated | relid=0 | w=20
  770. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:disorder of sulfur-bearing amino acid metabolism
    n1=en:classical phenylketonuria | n2=en:disorder of sulfur-bearing amino acid metabolism | rel=r_associated | relid=0 | w=20
  771. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:disorder of tryptophan metabolism
    n1=en:classical phenylketonuria | n2=en:disorder of tryptophan metabolism | rel=r_associated | relid=0 | w=20
  772. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Down syndrome
    n1=en:classical phenylketonuria | n2=en:Down syndrome | rel=r_associated | relid=0 | w=20
  773. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:dry skin
    n1=en:classical phenylketonuria | n2=en:dry skin | rel=r_associated | relid=0 | w=20
  774. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Dubin-Johnson's syndrome
    n1=en:classical phenylketonuria | n2=en:Dubin-Johnson's syndrome | rel=r_associated | relid=0 | w=20
  775. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Dubin-Sprinz disease
    n1=en:classical phenylketonuria | n2=en:Dubin-Sprinz disease | rel=r_associated | relid=0 | w=20
  776. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:dwarfism
    n1=en:classical phenylketonuria | n2=en:dwarfism | rel=r_associated | relid=0 | w=20
  777. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:dyslipidemia (in some patients)
    n1=en:classical phenylketonuria | n2=en:dyslipidemia (in some patients) | rel=r_associated | relid=0 | w=20
  778. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:dysmorphism
    n1=en:classical phenylketonuria | n2=en:dysmorphism | rel=r_associated | relid=0 | w=20
  779. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency
    n1=en:classical phenylketonuria | n2=en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency | rel=r_associated | relid=0 | w=20
  780. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:ectodermal dysplasia with blindness syndrome
    n1=en:classical phenylketonuria | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20
  781. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:ectopia cordis
    n1=en:classical phenylketonuria | n2=en:ectopia cordis | rel=r_associated | relid=0 | w=20
  782. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:ehlers-danlos syndrome kyphoscoliotic and deafness type
    n1=en:classical phenylketonuria | n2=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | rel=r_associated | relid=0 | w=20
  783. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:elevated alkaline phosphatase
    n1=en:classical phenylketonuria | n2=en:elevated alkaline phosphatase | rel=r_associated | relid=0 | w=20
  784. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:emanuel syndrome
    n1=en:classical phenylketonuria | n2=en:emanuel syndrome | rel=r_associated | relid=0 | w=20
  785. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:embryonic cyst
    n1=en:classical phenylketonuria | n2=en:embryonic cyst | rel=r_associated | relid=0 | w=20
  786. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:episodic ketoacidosis
    n1=en:classical phenylketonuria | n2=en:episodic ketoacidosis | rel=r_associated | relid=0 | w=20
  787. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:erythrocyte enolase deficiency
    n1=en:classical phenylketonuria | n2=en:erythrocyte enolase deficiency | rel=r_associated | relid=0 | w=20
  788. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:erythropoietic protoporphyria
    n1=en:classical phenylketonuria | n2=en:erythropoietic protoporphyria | rel=r_associated | relid=0 | w=20
  789. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:ethmocephaly
    n1=en:classical phenylketonuria | n2=en:ethmocephaly | rel=r_associated | relid=0 | w=20
  790. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:excessive thirst
    n1=en:classical phenylketonuria | n2=en:excessive thirst | rel=r_associated | relid=0 | w=20
  791. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:excretion of dicarboxylic acids
    n1=en:classical phenylketonuria | n2=en:excretion of dicarboxylic acids | rel=r_associated | relid=0 | w=20
  792. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:exencephaly
    n1=en:classical phenylketonuria | n2=en:exencephaly | rel=r_associated | relid=0 | w=20
  793. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:exenkephaly
    n1=en:classical phenylketonuria | n2=en:exenkephaly | rel=r_associated | relid=0 | w=20
  794. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:exertional hemoglobinuria
    n1=en:classical phenylketonuria | n2=en:exertional hemoglobinuria | rel=r_associated | relid=0 | w=20
  795. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:exomphalos
    n1=en:classical phenylketonuria | n2=en:exomphalos | rel=r_associated | relid=0 | w=20
  796. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:exstrophy
    n1=en:classical phenylketonuria | n2=en:exstrophy | rel=r_associated | relid=0 | w=20
  797. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:exumbilication
    n1=en:classical phenylketonuria | n2=en:exumbilication | rel=r_associated | relid=0 | w=20
  798. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:facial cleft
    n1=en:classical phenylketonuria | n2=en:facial cleft | rel=r_associated | relid=0 | w=20
  799. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Fallot's disease
    n1=en:classical phenylketonuria | n2=en:Fallot's disease | rel=r_associated | relid=0 | w=20
  800. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:familial median cleft of upper and lower lip
    n1=en:classical phenylketonuria | n2=en:familial median cleft of upper and lower lip | rel=r_associated | relid=0 | w=20
  801. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:fatty acid metabolism disorder
    n1=en:classical phenylketonuria | n2=en:fatty acid metabolism disorder | rel=r_associated | relid=0 | w=20
  802. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:fountain syndrome
    n1=en:classical phenylketonuria | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=20
  803. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:fragile X syndrome
    n1=en:classical phenylketonuria | n2=en:fragile X syndrome | rel=r_associated | relid=0 | w=20
  804. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:fried syndrome
    n1=en:classical phenylketonuria | n2=en:fried syndrome | rel=r_associated | relid=0 | w=20
  805. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:frohlich syndrome
    n1=en:classical phenylketonuria | n2=en:frohlich syndrome | rel=r_associated | relid=0 | w=20
  806. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:gastroschisis
    n1=en:classical phenylketonuria | n2=en:gastroschisis | rel=r_associated | relid=0 | w=20
  807. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Gaucher disease
    n1=en:classical phenylketonuria | n2=en:Gaucher disease | rel=r_associated | relid=0 | w=20
  808. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:generalized hypopigmentation
    n1=en:classical phenylketonuria | n2=en:generalized hypopigmentation | rel=r_associated | relid=0 | w=20
  809. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:generalized peeling skin syndrome
    n1=en:classical phenylketonuria | n2=en:generalized peeling skin syndrome | rel=r_associated | relid=0 | w=20
  810. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:genetic condition
    n1=en:classical phenylketonuria | n2=en:genetic condition | rel=r_associated | relid=0 | w=20
  811. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:genetic disease
    n1=en:classical phenylketonuria | n2=en:genetic disease | rel=r_associated | relid=0 | w=20
  812. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:genetic illness
    n1=en:classical phenylketonuria | n2=en:genetic illness | rel=r_associated | relid=0 | w=20
  813. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:gigantism and hyperplastic visceromegaly
    n1=en:classical phenylketonuria | n2=en:gigantism and hyperplastic visceromegaly | rel=r_associated | relid=0 | w=20
  814. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:glutaric acidemia type 1
    n1=en:classical phenylketonuria | n2=en:glutaric acidemia type 1 | rel=r_associated | relid=0 | w=20
  815. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:glutaric aciduria type 1
    n1=en:classical phenylketonuria | n2=en:glutaric aciduria type 1 | rel=r_associated | relid=0 | w=20
  816. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:glutaric aciduria, type 1
    n1=en:classical phenylketonuria | n2=en:glutaric aciduria, type 1 | rel=r_associated | relid=0 | w=20
  817. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:glutathione synthetase deficiency
    n1=en:classical phenylketonuria | n2=en:glutathione synthetase deficiency | rel=r_associated | relid=0 | w=20
  818. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:glycogen storage disease
    n1=en:classical phenylketonuria | n2=en:glycogen storage disease | rel=r_associated | relid=0 | w=20
  819. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
    n1=en:classical phenylketonuria | n2=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | rel=r_associated | relid=0 | w=20
  820. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:gout
    n1=en:classical phenylketonuria | n2=en:gout | rel=r_associated | relid=0 | w=20
  821. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:greig syndrome
    n1=en:classical phenylketonuria | n2=en:greig syndrome | rel=r_associated | relid=0 | w=20
  822. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:gustation
    n1=en:classical phenylketonuria | n2=en:gustation | rel=r_associated | relid=0 | w=20
  823. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hall riggs syndrome
    n1=en:classical phenylketonuria | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=20
  824. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hand and foot deformity
    n1=en:classical phenylketonuria | n2=en:hand and foot deformity | rel=r_associated | relid=0 | w=20
  825. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:harelip
    n1=en:classical phenylketonuria | n2=en:harelip | rel=r_associated | relid=0 | w=20
  826. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hartnup disease
    n1=en:classical phenylketonuria | n2=en:hartnup disease | rel=r_associated | relid=0 | w=20
  827. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:heart defects limb shortening
    n1=en:classical phenylketonuria | n2=en:heart defects limb shortening | rel=r_associated | relid=0 | w=20
  828. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:heart disease
    n1=en:classical phenylketonuria | n2=en:heart disease | rel=r_associated | relid=0 | w=20
  829. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:heart diseases
    n1=en:classical phenylketonuria | n2=en:heart diseases | rel=r_associated | relid=0 | w=20
  830. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:heart disorder
    n1=en:classical phenylketonuria | n2=en:heart disorder | rel=r_associated | relid=0 | w=20
  831. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:heat-stroke
    n1=en:classical phenylketonuria | n2=en:heat-stroke | rel=r_associated | relid=0 | w=20
  832. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hematuria
    n1=en:classical phenylketonuria | n2=en:hematuria | rel=r_associated | relid=0 | w=20
  833. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hereditary disease
    n1=en:classical phenylketonuria | n2=en:hereditary disease | rel=r_associated | relid=0 | w=20
  834. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hereditary elliptocytosis
    n1=en:classical phenylketonuria | n2=en:hereditary elliptocytosis | rel=r_associated | relid=0 | w=20
  835. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hereditary hyperbilirubinemia
    n1=en:classical phenylketonuria | n2=en:hereditary hyperbilirubinemia | rel=r_associated | relid=0 | w=20
  836. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:heterotaxy
    n1=en:classical phenylketonuria | n2=en:heterotaxy | rel=r_associated | relid=0 | w=20
  837. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:heterotaxy syndrome
    n1=en:classical phenylketonuria | n2=en:heterotaxy syndrome | rel=r_associated | relid=0 | w=20
  838. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hexose-6-phosphate dehydrogenase deficiency
    n1=en:classical phenylketonuria | n2=en:hexose-6-phosphate dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
  839. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hnsha due to hexokinase deficiency
    n1=en:classical phenylketonuria | n2=en:hnsha due to hexokinase deficiency | rel=r_associated | relid=0 | w=20
  840. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:holocarboxylase synthetase deficiency
    n1=en:classical phenylketonuria | n2=en:holocarboxylase synthetase deficiency | rel=r_associated | relid=0 | w=20
  841. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:homocarnosinosis
    n1=en:classical phenylketonuria | n2=en:homocarnosinosis | rel=r_associated | relid=0 | w=20
  842. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:homocystinemia
    n1=en:classical phenylketonuria | n2=en:homocystinemia | rel=r_associated | relid=0 | w=20
  843. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Huntington's disease
    n1=en:classical phenylketonuria | n2=en:Huntington's disease | rel=r_associated | relid=0 | w=20
  844. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hydrencephalus
    n1=en:classical phenylketonuria | n2=en:hydrencephalus | rel=r_associated | relid=0 | w=20
  845. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hydrocephalus
    n1=en:classical phenylketonuria | n2=en:hydrocephalus | rel=r_associated | relid=0 | w=20
  846. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hydroxyprolinemia
    n1=en:classical phenylketonuria | n2=en:hydroxyprolinemia | rel=r_associated | relid=0 | w=20
  847. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hyperandrogenism due to non-classic 21-hydroxylase deficiency
    n1=en:classical phenylketonuria | n2=en:hyperandrogenism due to non-classic 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=20
  848. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hypercholesterolemia (disorder)
    n1=en:classical phenylketonuria | n2=en:hypercholesterolemia (disorder) | rel=r_associated | relid=0 | w=20
  849. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hyperglycinemia
    n1=en:classical phenylketonuria | n2=en:hyperglycinemia | rel=r_associated | relid=0 | w=20
  850. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hyperhomocysteinemia
    n1=en:classical phenylketonuria | n2=en:hyperhomocysteinemia | rel=r_associated | relid=0 | w=20
  851. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hyperlipemia
    n1=en:classical phenylketonuria | n2=en:hyperlipemia | rel=r_associated | relid=0 | w=20
  852. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hyperlipidaemia
    n1=en:classical phenylketonuria | n2=en:hyperlipidaemia | rel=r_associated | relid=0 | w=20
  853. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hyperlipoproteinemia type i
    n1=en:classical phenylketonuria | n2=en:hyperlipoproteinemia type i | rel=r_associated | relid=0 | w=20
  854. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hyperphenylalaninaemia
    n1=en:classical phenylketonuria | n2=en:hyperphenylalaninaemia | rel=r_associated | relid=0 | w=20
  855. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hyperphenylalaninemia
    n1=en:classical phenylketonuria | n2=en:hyperphenylalaninemia | rel=r_associated | relid=0 | w=20
  856. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hyperphenylalaninemia, non phenylketonuric
    n1=en:classical phenylketonuria | n2=en:hyperphenylalaninemia, non phenylketonuric | rel=r_associated | relid=0 | w=20
  857. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hyperprolinemia
    n1=en:classical phenylketonuria | n2=en:hyperprolinemia | rel=r_associated | relid=0 | w=20
  858. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hypertelorism
    n1=en:classical phenylketonuria | n2=en:hypertelorism | rel=r_associated | relid=0 | w=20
  859. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hyperthermia
    n1=en:classical phenylketonuria | n2=en:hyperthermia | rel=r_associated | relid=0 | w=20
  860. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hyperthermy
    n1=en:classical phenylketonuria | n2=en:hyperthermy | rel=r_associated | relid=0 | w=20
  861. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hypertriglyceridemia
    n1=en:classical phenylketonuria | n2=en:hypertriglyceridemia | rel=r_associated | relid=0 | w=20
  862. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hypoglycaemic episode
    n1=en:classical phenylketonuria | n2=en:hypoglycaemic episode | rel=r_associated | relid=0 | w=20
  863. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hypoglycemia, oral protein-induced
    n1=en:classical phenylketonuria | n2=en:hypoglycemia, oral protein-induced | rel=r_associated | relid=0 | w=20
  864. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hypoketotic hypoglycemia
    n1=en:classical phenylketonuria | n2=en:hypoketotic hypoglycemia | rel=r_associated | relid=0 | w=20
  865. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hypomandibular faciocranial dysostosis
    n1=en:classical phenylketonuria | n2=en:hypomandibular faciocranial dysostosis | rel=r_associated | relid=0 | w=20
  866. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hypophosphatasia infantile
    n1=en:classical phenylketonuria | n2=en:hypophosphatasia infantile | rel=r_associated | relid=0 | w=20
  867. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hypopituitarism
    n1=en:classical phenylketonuria | n2=en:hypopituitarism | rel=r_associated | relid=0 | w=20
  868. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hypoplasia
    n1=en:classical phenylketonuria | n2=en:hypoplasia | rel=r_associated | relid=0 | w=20
  869. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:hypothalamic hamartoblastoma
    n1=en:classical phenylketonuria | n2=en:hypothalamic hamartoblastoma | rel=r_associated | relid=0 | w=20
  870. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:I-cell disease
    n1=en:classical phenylketonuria | n2=en:I-cell disease | rel=r_associated | relid=0 | w=20
  871. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:idiot
    n1=en:classical phenylketonuria | n2=en:idiot | rel=r_associated | relid=0 | w=20
  872. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:impairment of urinary concentration
    n1=en:classical phenylketonuria | n2=en:impairment of urinary concentration | rel=r_associated | relid=0 | w=20
  873. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:inborn error of glutathione metabolism
    n1=en:classical phenylketonuria | n2=en:inborn error of glutathione metabolism | rel=r_associated | relid=0 | w=20
  874. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:inborn error of lipoprotein metabolism
    n1=en:classical phenylketonuria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
  875. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:inborn errors of bilirubin metabolism
    n1=en:classical phenylketonuria | n2=en:inborn errors of bilirubin metabolism | rel=r_associated | relid=0 | w=20
  876. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:inborn errors of porphyrin metabolism
    n1=en:classical phenylketonuria | n2=en:inborn errors of porphyrin metabolism | rel=r_associated | relid=0 | w=20
  877. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:inborn errors of steroid synthesis
    n1=en:classical phenylketonuria | n2=en:inborn errors of steroid synthesis | rel=r_associated | relid=0 | w=20
  878. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:increased aromatase activity
    n1=en:classical phenylketonuria | n2=en:increased aromatase activity | rel=r_associated | relid=0 | w=20
  879. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:increased urinary o-hydroxyphenylacetic acid, phenylpyruvic acid, phenylacetic acid and phenylacetylglutamine
    n1=en:classical phenylketonuria | n2=en:increased urinary o-hydroxyphenylacetic acid, phenylpyruvic acid, phenylacetic acid and phenylacetylglutamine | rel=r_associated | relid=0 | w=20
  880. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:infection causing congenital anomaly
    n1=en:classical phenylketonuria | n2=en:infection causing congenital anomaly | rel=r_associated | relid=0 | w=20
  881. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:inherited disease
    n1=en:classical phenylketonuria | n2=en:inherited disease | rel=r_associated | relid=0 | w=20
  882. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:inherited disorder of folate metabolism
    n1=en:classical phenylketonuria | n2=en:inherited disorder of folate metabolism | rel=r_associated | relid=0 | w=20
  883. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:insulin growth factor i deficiency
    n1=en:classical phenylketonuria | n2=en:insulin growth factor i deficiency | rel=r_associated | relid=0 | w=20
  884. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:intermediary metabolism disorder
    n1=en:classical phenylketonuria | n2=en:intermediary metabolism disorder | rel=r_associated | relid=0 | w=20
  885. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:kallman syndrome with heart disease
    n1=en:classical phenylketonuria | n2=en:kallman syndrome with heart disease | rel=r_associated | relid=0 | w=20
  886. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:keratoconus posticus
    n1=en:classical phenylketonuria | n2=en:keratoconus posticus | rel=r_associated | relid=0 | w=20
  887. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:ketoacidosis
    n1=en:classical phenylketonuria | n2=en:ketoacidosis | rel=r_associated | relid=0 | w=20
  888. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:ketoses, metabolic
    n1=en:classical phenylketonuria | n2=en:ketoses, metabolic | rel=r_associated | relid=0 | w=20
  889. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Klinefelter syndrome
    n1=en:classical phenylketonuria | n2=en:Klinefelter syndrome | rel=r_associated | relid=0 | w=20
  890. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:known or suspected fetal abnormality affecting management of mother
    n1=en:classical phenylketonuria | n2=en:known or suspected fetal abnormality affecting management of mother | rel=r_associated | relid=0 | w=20
  891. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:kosztolanyi syndrome
    n1=en:classical phenylketonuria | n2=en:kosztolanyi syndrome | rel=r_associated | relid=0 | w=20
  892. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:labial fissure
    n1=en:classical phenylketonuria | n2=en:labial fissure | rel=r_associated | relid=0 | w=20
  893. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:lactose intolerance, adult type
    n1=en:classical phenylketonuria | n2=en:lactose intolerance, adult type | rel=r_associated | relid=0 | w=20
  894. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:laparoschisis
    n1=en:classical phenylketonuria | n2=en:laparoschisis | rel=r_associated | relid=0 | w=20
  895. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:late-onset junctional epidermolysis bullosa
    n1=en:classical phenylketonuria | n2=en:late-onset junctional epidermolysis bullosa | rel=r_associated | relid=0 | w=20
  896. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:learning disability
    n1=en:classical phenylketonuria | n2=en:learning disability | rel=r_associated | relid=0 | w=20
  897. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Leroy's i-cell disease
    n1=en:classical phenylketonuria | n2=en:Leroy's i-cell disease | rel=r_associated | relid=0 | w=20
  898. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:lethal larsen-like syndrome
    n1=en:classical phenylketonuria | n2=en:lethal larsen-like syndrome | rel=r_associated | relid=0 | w=20
  899. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:leucinosis
    n1=en:classical phenylketonuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  900. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:limb deformities, congenital
    n1=en:classical phenylketonuria | n2=en:limb deformities, congenital | rel=r_associated | relid=0 | w=20
  901. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:lipoid congenital adrenal hyperplasia
    n1=en:classical phenylketonuria | n2=en:lipoid congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=20
  902. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:lissencephaly type 3 familial fetal akinesia sequence syndrome
    n1=en:classical phenylketonuria | n2=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | rel=r_associated | relid=0 | w=20
  903. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Lowe's syndrome
    n1=en:classical phenylketonuria | n2=en:Lowe's syndrome | rel=r_associated | relid=0 | w=20
  904. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:lymphatic abnormalities
    n1=en:classical phenylketonuria | n2=en:lymphatic abnormalities | rel=r_associated | relid=0 | w=20
  905. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:lysinuric protein intolerance
    n1=en:classical phenylketonuria | n2=en:lysinuric protein intolerance | rel=r_associated | relid=0 | w=20
  906. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:macroglossia
    n1=en:classical phenylketonuria | n2=en:macroglossia | rel=r_associated | relid=0 | w=20
  907. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:major congenital anomaly
    n1=en:classical phenylketonuria | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  908. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:major physical defect
    n1=en:classical phenylketonuria | n2=en:major physical defect | rel=r_associated | relid=0 | w=20
  909. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:malignant hyperthermia syndrome
    n1=en:classical phenylketonuria | n2=en:malignant hyperthermia syndrome | rel=r_associated | relid=0 | w=20
  910. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:manouvrier syndrome
    n1=en:classical phenylketonuria | n2=en:manouvrier syndrome | rel=r_associated | relid=0 | w=20
  911. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:maple-tree syrup disease
    n1=en:classical phenylketonuria | n2=en:maple-tree syrup disease | rel=r_associated | relid=0 | w=20
  912. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:maternal hyperphenylalaninemia teratogenic
    n1=en:classical phenylketonuria | n2=en:maternal hyperphenylalaninemia teratogenic | rel=r_associated | relid=0 | w=20
  913. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:megaloglossia
    n1=en:classical phenylketonuria | n2=en:megaloglossia | rel=r_associated | relid=0 | w=20
  914. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency
    n1=en:classical phenylketonuria | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | rel=r_associated | relid=0 | w=20
  915. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:mental deficiency
    n1=en:classical phenylketonuria | n2=en:mental deficiency | rel=r_associated | relid=0 | w=20
  916. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:mental dullness
    n1=en:classical phenylketonuria | n2=en:mental dullness | rel=r_associated | relid=0 | w=20
  917. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:mental handicap
    n1=en:classical phenylketonuria | n2=en:mental handicap | rel=r_associated | relid=0 | w=20
  918. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:mental retardation spasticity ectrodactyly
    n1=en:classical phenylketonuria | n2=en:mental retardation spasticity ectrodactyly | rel=r_associated | relid=0 | w=20
  919. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:mental retardation syndrome, belgian type
    n1=en:classical phenylketonuria | n2=en:mental retardation syndrome, belgian type | rel=r_associated | relid=0 | w=20
  920. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome
    n1=en:classical phenylketonuria | n2=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | rel=r_associated | relid=0 | w=20
  921. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:metabolic decompensation during febrile illness (patient b)
    n1=en:classical phenylketonuria | n2=en:metabolic decompensation during febrile illness (patient b) | rel=r_associated | relid=0 | w=20
  922. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:methylenetetrahydrofolate reductase gene mutation
    n1=en:classical phenylketonuria | n2=en:methylenetetrahydrofolate reductase gene mutation | rel=r_associated | relid=0 | w=20
  923. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:mevalonic aciduria
    n1=en:classical phenylketonuria | n2=en:mevalonic aciduria | rel=r_associated | relid=0 | w=20
  924. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:microcephaly albinism digital anomalies syndrome
    n1=en:classical phenylketonuria | n2=en:microcephaly albinism digital anomalies syndrome | rel=r_associated | relid=0 | w=20
  925. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:mildly elevated glucose
    n1=en:classical phenylketonuria | n2=en:mildly elevated glucose | rel=r_associated | relid=0 | w=20
  926. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:monopia
    n1=en:classical phenylketonuria | n2=en:monopia | rel=r_associated | relid=0 | w=20
  927. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:monster (disorder)
    n1=en:classical phenylketonuria | n2=en:monster (disorder) | rel=r_associated | relid=0 | w=20
  928. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:moyamoya disease with early onset achalasia
    n1=en:classical phenylketonuria | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=20
  929. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:mucopolysaccharidosis i
    n1=en:classical phenylketonuria | n2=en:mucopolysaccharidosis i | rel=r_associated | relid=0 | w=20
  930. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:multiple acyl-coa dehydrogenase deficiency
    n1=en:classical phenylketonuria | n2=en:multiple acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
  931. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:multiple carboxylase deficiency
    n1=en:classical phenylketonuria | n2=en:multiple carboxylase deficiency | rel=r_associated | relid=0 | w=20
  932. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:muscle d-lactate dehydrogenase deficiency
    n1=en:classical phenylketonuria | n2=en:muscle d-lactate dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
  933. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:myoglobinuria, recurrent
    n1=en:classical phenylketonuria | n2=en:myoglobinuria, recurrent | rel=r_associated | relid=0 | w=20
  934. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:najjar syndrome
    n1=en:classical phenylketonuria | n2=en:najjar syndrome | rel=r_associated | relid=0 | w=20
  935. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:neonatal disorder
    n1=en:classical phenylketonuria | n2=en:neonatal disorder | rel=r_associated | relid=0 | w=20
  936. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:neonatal hemochromatosis
    n1=en:classical phenylketonuria | n2=en:neonatal hemochromatosis | rel=r_associated | relid=0 | w=20
  937. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:neonatal hypoglycemia
    n1=en:classical phenylketonuria | n2=en:neonatal hypoglycemia | rel=r_associated | relid=0 | w=20
  938. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:neurodevelopmental anomaly
    n1=en:classical phenylketonuria | n2=en:neurodevelopmental anomaly | rel=r_associated | relid=0 | w=20
  939. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Niemann-Pick disease
    n1=en:classical phenylketonuria | n2=en:Niemann-Pick disease | rel=r_associated | relid=0 | w=20
  940. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:nonketotic hypoglycemia
    n1=en:classical phenylketonuria | n2=en:nonketotic hypoglycemia | rel=r_associated | relid=0 | w=20
  941. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:normal blood lactate levels (in both patients)
    n1=en:classical phenylketonuria | n2=en:normal blood lactate levels (in both patients) | rel=r_associated | relid=0 | w=20
  942. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:normal sweating
    n1=en:classical phenylketonuria | n2=en:normal sweating | rel=r_associated | relid=0 | w=20
  943. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:normalization of metabolic parameters in between crises
    n1=en:classical phenylketonuria | n2=en:normalization of metabolic parameters in between crises | rel=r_associated | relid=0 | w=20
  944. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:oculocutaneous albinism type 6
    n1=en:classical phenylketonuria | n2=en:oculocutaneous albinism type 6 | rel=r_associated | relid=0 | w=20
  945. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:ombilical hernia
    n1=en:classical phenylketonuria | n2=en:ombilical hernia | rel=r_associated | relid=0 | w=20
  946. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:omphalocele
    n1=en:classical phenylketonuria | n2=en:omphalocele | rel=r_associated | relid=0 | w=20
  947. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:other congenital anomalies of nervous system
    n1=en:classical phenylketonuria | n2=en:other congenital anomalies of nervous system | rel=r_associated | relid=0 | w=20
  948. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:other disorders of aromatic amino-acid metabolism
    n1=en:classical phenylketonuria | n2=en:other disorders of aromatic amino-acid metabolism | rel=r_associated | relid=0 | w=20
  949. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:other disturbances of straight-chain amino-acid metabolism
    n1=en:classical phenylketonuria | n2=en:other disturbances of straight-chain amino-acid metabolism | rel=r_associated | relid=0 | w=20
  950. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:other hyperphenylalaninaemias
    n1=en:classical phenylketonuria | n2=en:other hyperphenylalaninaemias | rel=r_associated | relid=0 | w=20
  951. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:other specified congenital malformations
    n1=en:classical phenylketonuria | n2=en:other specified congenital malformations | rel=r_associated | relid=0 | w=20
  952. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:other specified disorders of amino-acid metabolism
    n1=en:classical phenylketonuria | n2=en:other specified disorders of amino-acid metabolism | rel=r_associated | relid=0 | w=20
  953. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:other specified disorders of amino-acid transport and metabolism
    n1=en:classical phenylketonuria | n2=en:other specified disorders of amino-acid transport and metabolism | rel=r_associated | relid=0 | w=20
  954. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:other specified mental retardation
    n1=en:classical phenylketonuria | n2=en:other specified mental retardation | rel=r_associated | relid=0 | w=20
  955. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:otocephaly
    n1=en:classical phenylketonuria | n2=en:otocephaly | rel=r_associated | relid=0 | w=20
  956. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:oxalosis
    n1=en:classical phenylketonuria | n2=en:oxalosis | rel=r_associated | relid=0 | w=20
  957. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:palate-blepharophimosis
    n1=en:classical phenylketonuria | n2=en:palate-blepharophimosis | rel=r_associated | relid=0 | w=20
  958. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome
    n1=en:classical phenylketonuria | n2=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | rel=r_associated | relid=0 | w=20
  959. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:pancreatic alpha-amylase deficiency
    n1=en:classical phenylketonuria | n2=en:pancreatic alpha-amylase deficiency | rel=r_associated | relid=0 | w=20
  960. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:pelviscapular dysplasia
    n1=en:classical phenylketonuria | n2=en:pelviscapular dysplasia | rel=r_associated | relid=0 | w=20
  961. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:peroxisomal disorder
    n1=en:classical phenylketonuria | n2=en:peroxisomal disorder | rel=r_associated | relid=0 | w=20
  962. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:phenylalanine-free diet education
    n1=en:classical phenylketonuria | n2=en:phenylalanine-free diet education | rel=r_associated | relid=0 | w=20
  963. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:phenylketonuria diet education
    n1=en:classical phenylketonuria | n2=en:phenylketonuria diet education | rel=r_associated | relid=0 | w=20
  964. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:phenylketonuria screening test
    n1=en:classical phenylketonuria | n2=en:phenylketonuria screening test | rel=r_associated | relid=0 | w=20
  965. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:phenylketonuria, maternal
    n1=en:classical phenylketonuria | n2=en:phenylketonuria, maternal | rel=r_associated | relid=0 | w=20
  966. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:phenylpyruvic oligophrenia
    n1=en:classical phenylketonuria | n2=en:phenylpyruvic oligophrenia | rel=r_associated | relid=0 | w=20
  967. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:photomyoclonus
    n1=en:classical phenylketonuria | n2=en:photomyoclonus | rel=r_associated | relid=0 | w=20
  968. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:physical defect
    n1=en:classical phenylketonuria | n2=en:physical defect | rel=r_associated | relid=0 | w=20
  969. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:pili torti onychodysplasia syndrome
    n1=en:classical phenylketonuria | n2=en:pili torti onychodysplasia syndrome | rel=r_associated | relid=0 | w=20
  970. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:piussan lenaerts mathieu syndrome
    n1=en:classical phenylketonuria | n2=en:piussan lenaerts mathieu syndrome | rel=r_associated | relid=0 | w=20
  971. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:polydipsia
    n1=en:classical phenylketonuria | n2=en:polydipsia | rel=r_associated | relid=0 | w=20
  972. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:porphyrinuria
    n1=en:classical phenylketonuria | n2=en:porphyrinuria | rel=r_associated | relid=0 | w=20
  973. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:posterior urethral valve
    n1=en:classical phenylketonuria | n2=en:posterior urethral valve | rel=r_associated | relid=0 | w=20
  974. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:ppp2r5d-related intellectual disability
    n1=en:classical phenylketonuria | n2=en:ppp2r5d-related intellectual disability | rel=r_associated | relid=0 | w=20
  975. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Prader-Willi syndrome
    n1=en:classical phenylketonuria | n2=en:Prader-Willi syndrome | rel=r_associated | relid=0 | w=20
  976. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:primary immunodeficiency syndrome due to p14 deficiency
    n1=en:classical phenylketonuria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20
  977. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:proctatresia
    n1=en:classical phenylketonuria | n2=en:proctatresia | rel=r_associated | relid=0 | w=20
  978. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:progeria
    n1=en:classical phenylketonuria | n2=en:progeria | rel=r_associated | relid=0 | w=20
  979. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:pterygium colli syndrome
    n1=en:classical phenylketonuria | n2=en:pterygium colli syndrome | rel=r_associated | relid=0 | w=20
  980. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:pyloric obstruction
    n1=en:classical phenylketonuria | n2=en:pyloric obstruction | rel=r_associated | relid=0 | w=20
  981. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:pyloric stenosis
    n1=en:classical phenylketonuria | n2=en:pyloric stenosis | rel=r_associated | relid=0 | w=20
  982. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:pyridoxine dependency syndrome
    n1=en:classical phenylketonuria | n2=en:pyridoxine dependency syndrome | rel=r_associated | relid=0 | w=20
  983. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:pyruvate dehydrogenase deficiency
    n1=en:classical phenylketonuria | n2=en:pyruvate dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
  984. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:radiation-induced disorder
    n1=en:classical phenylketonuria | n2=en:radiation-induced disorder | rel=r_associated | relid=0 | w=20
  985. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:recurrent hypoglycemia
    n1=en:classical phenylketonuria | n2=en:recurrent hypoglycemia | rel=r_associated | relid=0 | w=20
  986. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:reduced energy expenditure
    n1=en:classical phenylketonuria | n2=en:reduced energy expenditure | rel=r_associated | relid=0 | w=20
  987. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:renal aminoacidurias
    n1=en:classical phenylketonuria | n2=en:renal aminoacidurias | rel=r_associated | relid=0 | w=20
  988. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:renal dysplasia - limb defects syndrome
    n1=en:classical phenylketonuria | n2=en:renal dysplasia - limb defects syndrome | rel=r_associated | relid=0 | w=20
  989. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:renal tubulopathy
    n1=en:classical phenylketonuria | n2=en:renal tubulopathy | rel=r_associated | relid=0 | w=20
  990. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:retardation
    n1=en:classical phenylketonuria | n2=en:retardation | rel=r_associated | relid=0 | w=20
  991. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:rheumatic chorea
    n1=en:classical phenylketonuria | n2=en:rheumatic chorea | rel=r_associated | relid=0 | w=20
  992. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:robinow-like syndrome
    n1=en:classical phenylketonuria | n2=en:robinow-like syndrome | rel=r_associated | relid=0 | w=20
  993. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:schinzel-giedion midface-retraction syndrome
    n1=en:classical phenylketonuria | n2=en:schinzel-giedion midface-retraction syndrome | rel=r_associated | relid=0 | w=20
  994. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:scholte syndrome
    n1=en:classical phenylketonuria | n2=en:scholte syndrome | rel=r_associated | relid=0 | w=20
  995. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:short stature
    n1=en:classical phenylketonuria | n2=en:short stature | rel=r_associated | relid=0 | w=20
  996. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:single congenital anomaly
    n1=en:classical phenylketonuria | n2=en:single congenital anomaly | rel=r_associated | relid=0 | w=20
  997. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:situs inversus
    n1=en:classical phenylketonuria | n2=en:situs inversus | rel=r_associated | relid=0 | w=20
  998. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:situs inversus viscerum
    n1=en:classical phenylketonuria | n2=en:situs inversus viscerum | rel=r_associated | relid=0 | w=20
  999. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:situs mutatus
    n1=en:classical phenylketonuria | n2=en:situs mutatus | rel=r_associated | relid=0 | w=20
  1000. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:sjogren-larsson syndrome
    n1=en:classical phenylketonuria | n2=en:sjogren-larsson syndrome | rel=r_associated | relid=0 | w=20
  1001. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:specific enzyme deficiency
    n1=en:classical phenylketonuria | n2=en:specific enzyme deficiency | rel=r_associated | relid=0 | w=20
  1002. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:split-hand/foot malformation 3
    n1=en:classical phenylketonuria | n2=en:split-hand/foot malformation 3 | rel=r_associated | relid=0 | w=20
  1003. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:spondyloepiphyseal dysplasia tarda kohn type
    n1=en:classical phenylketonuria | n2=en:spondyloepiphyseal dysplasia tarda kohn type | rel=r_associated | relid=0 | w=20
  1004. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome
    n1=en:classical phenylketonuria | n2=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | rel=r_associated | relid=0 | w=20
  1005. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:steroid metabolism, inborn errors
    n1=en:classical phenylketonuria | n2=en:steroid metabolism, inborn errors | rel=r_associated | relid=0 | w=20
  1006. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:stomatognathic system abnormalities
    n1=en:classical phenylketonuria | n2=en:stomatognathic system abnormalities | rel=r_associated | relid=0 | w=20
  1007. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:storage disease
    n1=en:classical phenylketonuria | n2=en:storage disease | rel=r_associated | relid=0 | w=20
  1008. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:strabismus syndrome
    n1=en:classical phenylketonuria | n2=en:strabismus syndrome | rel=r_associated | relid=0 | w=20
  1009. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:sugar diabetes
    n1=en:classical phenylketonuria | n2=en:sugar diabetes | rel=r_associated | relid=0 | w=20
  1010. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:supernumerary structure
    n1=en:classical phenylketonuria | n2=en:supernumerary structure | rel=r_associated | relid=0 | w=20
  1011. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Sydenham's chorea
    n1=en:classical phenylketonuria | n2=en:Sydenham's chorea | rel=r_associated | relid=0 | w=20
  1012. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:taste perception
    n1=en:classical phenylketonuria | n2=en:taste perception | rel=r_associated | relid=0 | w=20
  1013. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Tay-Sachs disease
    n1=en:classical phenylketonuria | n2=en:Tay-Sachs disease | rel=r_associated | relid=0 | w=20
  1014. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:telecanthus
    n1=en:classical phenylketonuria | n2=en:telecanthus | rel=r_associated | relid=0 | w=20
  1015. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:teratosis
    n1=en:classical phenylketonuria | n2=en:teratosis | rel=r_associated | relid=0 | w=20
  1016. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:tetralogy
    n1=en:classical phenylketonuria | n2=en:tetralogy | rel=r_associated | relid=0 | w=20
  1017. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:tetralogy of Fallot
    n1=en:classical phenylketonuria | n2=en:tetralogy of Fallot | rel=r_associated | relid=0 | w=20
  1018. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:tetralogy of fallot
    n1=en:classical phenylketonuria | n2=en:tetralogy of fallot | rel=r_associated | relid=0 | w=20
  1019. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:thiamin-responsive maple syrup urine disease
    n1=en:classical phenylketonuria | n2=en:thiamin-responsive maple syrup urine disease | rel=r_associated | relid=0 | w=20
  1020. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:thyroid dysgenesis
    n1=en:classical phenylketonuria | n2=en:thyroid dysgenesis | rel=r_associated | relid=0 | w=20
  1021. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:transitory amino acid metabolic disorder
    n1=en:classical phenylketonuria | n2=en:transitory amino acid metabolic disorder | rel=r_associated | relid=0 | w=20
  1022. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:trichorhinophalangeal syndrome type ii
    n1=en:classical phenylketonuria | n2=en:trichorhinophalangeal syndrome type ii | rel=r_associated | relid=0 | w=20
  1023. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:trichorhinophalangeal syndrome type II
    n1=en:classical phenylketonuria | n2=en:trichorhinophalangeal syndrome type II | rel=r_associated | relid=0 | w=20
  1024. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:trisomy 14
    n1=en:classical phenylketonuria | n2=en:trisomy 14 | rel=r_associated | relid=0 | w=20
  1025. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:trisomy 17
    n1=en:classical phenylketonuria | n2=en:trisomy 17 | rel=r_associated | relid=0 | w=20
  1026. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:trisomy xq28 syndrome
    n1=en:classical phenylketonuria | n2=en:trisomy xq28 syndrome | rel=r_associated | relid=0 | w=20
  1027. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:ugt1a1*28 polymorphism
    n1=en:classical phenylketonuria | n2=en:ugt1a1*28 polymorphism | rel=r_associated | relid=0 | w=20
  1028. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Umbilical hernia
    n1=en:classical phenylketonuria | n2=en:Umbilical hernia | rel=r_associated | relid=0 | w=20
  1029. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:umbilical hernia
    n1=en:classical phenylketonuria | n2=en:umbilical hernia | rel=r_associated | relid=0 | w=20
  1030. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:unclassified metabolic disorder
    n1=en:classical phenylketonuria | n2=en:unclassified metabolic disorder | rel=r_associated | relid=0 | w=20
  1031. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:urea cycle metabolism disorder
    n1=en:classical phenylketonuria | n2=en:urea cycle metabolism disorder | rel=r_associated | relid=0 | w=20
  1032. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:ureterocele
    n1=en:classical phenylketonuria | n2=en:ureterocele | rel=r_associated | relid=0 | w=20
  1033. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:urinary abnormalities
    n1=en:classical phenylketonuria | n2=en:urinary abnormalities | rel=r_associated | relid=0 | w=20
  1034. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:urine casts
    n1=en:classical phenylketonuria | n2=en:urine casts | rel=r_associated | relid=0 | w=20
  1035. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:uroglycosis
    n1=en:classical phenylketonuria | n2=en:uroglycosis | rel=r_associated | relid=0 | w=20
  1036. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:ventriculomeglia
    n1=en:classical phenylketonuria | n2=en:ventriculomeglia | rel=r_associated | relid=0 | w=20
  1037. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Williams syndrome
    n1=en:classical phenylketonuria | n2=en:Williams syndrome | rel=r_associated | relid=0 | w=20
  1038. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:williams syndrome
    n1=en:classical phenylketonuria | n2=en:williams syndrome | rel=r_associated | relid=0 | w=20
  1039. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome
    n1=en:classical phenylketonuria | n2=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome | rel=r_associated | relid=0 | w=20
  1040. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Wolman's disease
    n1=en:classical phenylketonuria | n2=en:Wolman's disease | rel=r_associated | relid=0 | w=20
  1041. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability armfield type
    n1=en:classical phenylketonuria | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
  1042. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability cantagrel type
    n1=en:classical phenylketonuria | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20
  1043. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability miles carpenter type
    n1=en:classical phenylketonuria | n2=en:x-linked intellectual disability miles carpenter type | rel=r_associated | relid=0 | w=20
  1044. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability pai type
    n1=en:classical phenylketonuria | n2=en:x-linked intellectual disability pai type | rel=r_associated | relid=0 | w=20
  1045. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability seemanova type
    n1=en:classical phenylketonuria | n2=en:x-linked intellectual disability seemanova type | rel=r_associated | relid=0 | w=20
  1046. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability stevenson type
    n1=en:classical phenylketonuria | n2=en:x-linked intellectual disability stevenson type | rel=r_associated | relid=0 | w=20
  1047. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability stoll type
    n1=en:classical phenylketonuria | n2=en:x-linked intellectual disability stoll type | rel=r_associated | relid=0 | w=20
  1048. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability van esch type
    n1=en:classical phenylketonuria | n2=en:x-linked intellectual disability van esch type | rel=r_associated | relid=0 | w=20
  1049. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability with acromegaly and hyperactivity syndrome
    n1=en:classical phenylketonuria | n2=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | rel=r_associated | relid=0 | w=20
  1050. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome
    n1=en:classical phenylketonuria | n2=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | rel=r_associated | relid=0 | w=20
  1051. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome
    n1=en:classical phenylketonuria | n2=en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome | rel=r_associated | relid=0 | w=20
  1052. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:yemenite deaf-blind hypopigmentation syndrome
    n1=en:classical phenylketonuria | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=20
  1053. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:Zellweger syndrome
    n1=en:classical phenylketonuria | n2=en:Zellweger syndrome | rel=r_associated | relid=0 | w=20
  1054. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:zellweger-like syndrome without peroxisomal anomaly
    n1=en:classical phenylketonuria | n2=en:zellweger-like syndrome without peroxisomal anomaly | rel=r_associated | relid=0 | w=20
  1055. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> en:zinc-deficiency type
    n1=en:classical phenylketonuria | n2=en:zinc-deficiency type | rel=r_associated | relid=0 | w=20
  1056. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> exéma
    n1=en:classical phenylketonuria | n2=exéma | rel=r_associated | relid=0 | w=20
  1057. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> exencéphalie
    n1=en:classical phenylketonuria | n2=exencéphalie | rel=r_associated | relid=0 | w=20
  1058. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> exomphale
    n1=en:classical phenylketonuria | n2=exomphale | rel=r_associated | relid=0 | w=20
  1059. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> exomphale congénitale
    n1=en:classical phenylketonuria | n2=exomphale congénitale | rel=r_associated | relid=0 | w=20
  1060. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> exstrophie
    n1=en:classical phenylketonuria | n2=exstrophie | rel=r_associated | relid=0 | w=20
  1061. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> faciès anormal, retard de croissance et retard mental
    n1=en:classical phenylketonuria | n2=faciès anormal, retard de croissance et retard mental | rel=r_associated | relid=0 | w=20
  1062. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Fenn (diagramme de)
    n1=en:classical phenylketonuria | n2=Fenn (diagramme de) | rel=r_associated | relid=0 | w=20
  1063. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> fente labiale
    n1=en:classical phenylketonuria | n2=fente labiale | rel=r_associated | relid=0 | w=20
  1064. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> fente labiopalatine et blépharophimosis
    n1=en:classical phenylketonuria | n2=fente labiopalatine et blépharophimosis | rel=r_associated | relid=0 | w=20
  1065. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> fente palatine
    n1=en:classical phenylketonuria | n2=fente palatine | rel=r_associated | relid=0 | w=20
  1066. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> fever
    n1=en:classical phenylketonuria | n2=fever | rel=r_associated | relid=0 | w=20
  1067. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> fissure faciale
    n1=en:classical phenylketonuria | n2=fissure faciale | rel=r_associated | relid=0 | w=20
  1068. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> fissure palatine
    n1=en:classical phenylketonuria | n2=fissure palatine | rel=r_associated | relid=0 | w=20
  1069. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> fucosidose
    n1=en:classical phenylketonuria | n2=fucosidose | rel=r_associated | relid=0 | w=20
  1070. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> gastroschisis
    n1=en:classical phenylketonuria | n2=gastroschisis | rel=r_associated | relid=0 | w=20
  1071. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> globulinurie
    n1=en:classical phenylketonuria | n2=globulinurie | rel=r_associated | relid=0 | w=20
  1072. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> goniodysgénésie-retard mental-petite taille (syndrome)
    n1=en:classical phenylketonuria | n2=goniodysgénésie-retard mental-petite taille (syndrome) | rel=r_associated | relid=0 | w=20
  1073. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> gout
    n1=en:classical phenylketonuria | n2=gout | rel=r_associated | relid=0 | w=20
  1074. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> goutte
    n1=en:classical phenylketonuria | n2=goutte | rel=r_associated | relid=0 | w=20
  1075. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> goutte
    (maladie)
    n1=en:classical phenylketonuria | n2=goutte
    (maladie)
    | rel=r_associated | relid=0 | w=20
  1076. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale
    n1=en:classical phenylketonuria | n2=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | rel=r_associated | relid=0 | w=20
  1077. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hématurie macroscopique
    n1=en:classical phenylketonuria | n2=hématurie macroscopique | rel=r_associated | relid=0 | w=20
  1078. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hémochromatose néonatale
    n1=en:classical phenylketonuria | n2=hémochromatose néonatale | rel=r_associated | relid=0 | w=20
  1079. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hémoglobinurie d'effort
    n1=en:classical phenylketonuria | n2=hémoglobinurie d'effort | rel=r_associated | relid=0 | w=20
  1080. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hérédité autosomale récessive
    n1=en:classical phenylketonuria | n2=hérédité autosomale récessive | rel=r_associated | relid=0 | w=20
  1081. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle
    n1=en:classical phenylketonuria | n2=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | rel=r_associated | relid=0 | w=20
  1082. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hernie ombilicale
    n1=en:classical phenylketonuria | n2=hernie ombilicale | rel=r_associated | relid=0 | w=20
  1083. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hernie ombilicale congénitale
    n1=en:classical phenylketonuria | n2=hernie ombilicale congénitale | rel=r_associated | relid=0 | w=20
  1084. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hernies ombilicales
    n1=en:classical phenylketonuria | n2=hernies ombilicales | rel=r_associated | relid=0 | w=20
  1085. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hétérotaxie
    n1=en:classical phenylketonuria | n2=hétérotaxie | rel=r_associated | relid=0 | w=20
  1086. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> histidinémie
    n1=en:classical phenylketonuria | n2=histidinémie | rel=r_associated | relid=0 | w=20
  1087. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> histiocytose sinusale hémophagocytaire
    n1=en:classical phenylketonuria | n2=histiocytose sinusale hémophagocytaire | rel=r_associated | relid=0 | w=20
  1088. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> homocarnosinose
    n1=en:classical phenylketonuria | n2=homocarnosinose | rel=r_associated | relid=0 | w=20
  1089. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hydrocéphalie
    n1=en:classical phenylketonuria | n2=hydrocéphalie | rel=r_associated | relid=0 | w=20
  1090. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hydroxyprolinémie
    n1=en:classical phenylketonuria | n2=hydroxyprolinémie | rel=r_associated | relid=0 | w=20
  1091. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hypercalciurie
    n1=en:classical phenylketonuria | n2=hypercalciurie | rel=r_associated | relid=0 | w=20
  1092. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hyperlipémie
    n1=en:classical phenylketonuria | n2=hyperlipémie | rel=r_associated | relid=0 | w=20
  1093. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hyperlipidémie
    n1=en:classical phenylketonuria | n2=hyperlipidémie | rel=r_associated | relid=0 | w=20
  1094. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hyperoxalurie primaire
    n1=en:classical phenylketonuria | n2=hyperoxalurie primaire | rel=r_associated | relid=0 | w=20
  1095. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hyperoxalurie primitive
    n1=en:classical phenylketonuria | n2=hyperoxalurie primitive | rel=r_associated | relid=0 | w=20
  1096. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hyperperméabilité capillaire (syndrome d')
    n1=en:classical phenylketonuria | n2=hyperperméabilité capillaire (syndrome d') | rel=r_associated | relid=0 | w=20
  1097. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hyperphénylalaninémie
    n1=en:classical phenylketonuria | n2=hyperphénylalaninémie | rel=r_associated | relid=0 | w=20
  1098. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hyperphosphaturie
    n1=en:classical phenylketonuria | n2=hyperphosphaturie | rel=r_associated | relid=0 | w=20
  1099. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hyperplasie congénitale des surrénales
    n1=en:classical phenylketonuria | n2=hyperplasie congénitale des surrénales | rel=r_associated | relid=0 | w=20
  1100. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hyperprolinémie
    n1=en:classical phenylketonuria | n2=hyperprolinémie | rel=r_associated | relid=0 | w=20
  1101. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hyperprolinémie de type I
    n1=en:classical phenylketonuria | n2=hyperprolinémie de type I | rel=r_associated | relid=0 | w=20
  1102. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hypertélorisme
    n1=en:classical phenylketonuria | n2=hypertélorisme | rel=r_associated | relid=0 | w=20
  1103. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hypertélorisme-microtie-fente faciale
    n1=en:classical phenylketonuria | n2=hypertélorisme-microtie-fente faciale | rel=r_associated | relid=0 | w=20
  1104. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hypertélorisme, hypospadias, polysyndactylie (syndrome)
    n1=en:classical phenylketonuria | n2=hypertélorisme, hypospadias, polysyndactylie (syndrome) | rel=r_associated | relid=0 | w=20
  1105. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hypertriglycéridémie
    n1=en:classical phenylketonuria | n2=hypertriglycéridémie | rel=r_associated | relid=0 | w=20
  1106. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hypertrophie staturale avec macroglossie et omphalocèle
    n1=en:classical phenylketonuria | n2=hypertrophie staturale avec macroglossie et omphalocèle | rel=r_associated | relid=0 | w=20
  1107. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hypoglycémie du nouveau-né
    n1=en:classical phenylketonuria | n2=hypoglycémie du nouveau-né | rel=r_associated | relid=0 | w=20
  1108. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hyponatriurie
    n1=en:classical phenylketonuria | n2=hyponatriurie | rel=r_associated | relid=0 | w=20
  1109. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hypophosphatasie foetale
    n1=en:classical phenylketonuria | n2=hypophosphatasie foetale | rel=r_associated | relid=0 | w=20
  1110. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hypophosphatasie infantile
    n1=en:classical phenylketonuria | n2=hypophosphatasie infantile | rel=r_associated | relid=0 | w=20
  1111. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> hypoplasie
    n1=en:classical phenylketonuria | n2=hypoplasie | rel=r_associated | relid=0 | w=20
  1112. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> idiotie xérodermique
    n1=en:classical phenylketonuria | n2=idiotie xérodermique | rel=r_associated | relid=0 | w=20
  1113. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> imperforation anale
    n1=en:classical phenylketonuria | n2=imperforation anale | rel=r_associated | relid=0 | w=20
  1114. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> imperforation de l'anus
    n1=en:classical phenylketonuria | n2=imperforation de l'anus | rel=r_associated | relid=0 | w=20
  1115. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> intolérance au fructose
    n1=en:classical phenylketonuria | n2=intolérance au fructose | rel=r_associated | relid=0 | w=20
  1116. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> isosthénurie
    n1=en:classical phenylketonuria | n2=isosthénurie | rel=r_associated | relid=0 | w=20
  1117. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> jumeaux fusionnés
    n1=en:classical phenylketonuria | n2=jumeaux fusionnés | rel=r_associated | relid=0 | w=20
  1118. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> jumeaux siamois
    n1=en:classical phenylketonuria | n2=jumeaux siamois | rel=r_associated | relid=0 | w=20
  1119. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> kératocône postérieur-fente labiale-petite taille
    n1=en:classical phenylketonuria | n2=kératocône postérieur-fente labiale-petite taille | rel=r_associated | relid=0 | w=20
  1120. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> laparoschisis
    n1=en:classical phenylketonuria | n2=laparoschisis | rel=r_associated | relid=0 | w=20
  1121. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> leucinose
    n1=en:classical phenylketonuria | n2=leucinose | rel=r_associated | relid=0 | w=20
  1122. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> lipofuscinose neuronale céroïde
    n1=en:classical phenylketonuria | n2=lipofuscinose neuronale céroïde | rel=r_associated | relid=0 | w=20
  1123. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> lipofuscinose neuronale céroïde infantile finlandaise
    n1=en:classical phenylketonuria | n2=lipofuscinose neuronale céroïde infantile finlandaise | rel=r_associated | relid=0 | w=20
  1124. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> macroglossie
    n1=en:classical phenylketonuria | n2=macroglossie | rel=r_associated | relid=0 | w=20
  1125. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie cardiaque
    n1=en:classical phenylketonuria | n2=maladie cardiaque | rel=r_associated | relid=0 | w=20
  1126. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie cardiaque non précisée
    n1=en:classical phenylketonuria | n2=maladie cardiaque non précisée | rel=r_associated | relid=0 | w=20
  1127. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie congénitale
    n1=en:classical phenylketonuria | n2=maladie congénitale | rel=r_associated | relid=0 | w=20
  1128. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Maladie congénitale
    n1=en:classical phenylketonuria | n2=Maladie congénitale | rel=r_associated | relid=0 | w=20
  1129. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie de coeur
    n1=en:classical phenylketonuria | n2=maladie de coeur | rel=r_associated | relid=0 | w=20
  1130. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie de dubin-johnson
    n1=en:classical phenylketonuria | n2=maladie de dubin-johnson | rel=r_associated | relid=0 | w=20
  1131. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie de Gaucher
    n1=en:classical phenylketonuria | n2=maladie de Gaucher | rel=r_associated | relid=0 | w=20
  1132. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie de Huntington
    n1=en:classical phenylketonuria | n2=maladie de Huntington | rel=r_associated | relid=0 | w=20
  1133. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Maladie de Huntington
    n1=en:classical phenylketonuria | n2=Maladie de Huntington | rel=r_associated | relid=0 | w=20
  1134. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie de marchiafava-micheli
    n1=en:classical phenylketonuria | n2=maladie de marchiafava-micheli | rel=r_associated | relid=0 | w=20
  1135. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie de Marchiafava-Micheli
    n1=en:classical phenylketonuria | n2=maladie de Marchiafava-Micheli | rel=r_associated | relid=0 | w=20
  1136. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie de Niemann-Pick
    n1=en:classical phenylketonuria | n2=maladie de Niemann-Pick | rel=r_associated | relid=0 | w=20
  1137. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie de Roger
    n1=en:classical phenylketonuria | n2=maladie de Roger | rel=r_associated | relid=0 | w=20
  1138. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie de surcharge
    n1=en:classical phenylketonuria | n2=maladie de surcharge | rel=r_associated | relid=0 | w=20
  1139. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie de Tay-Sachs
    n1=en:classical phenylketonuria | n2=maladie de Tay-Sachs | rel=r_associated | relid=0 | w=20
  1140. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie de tay-sachs
    n1=en:classical phenylketonuria | n2=maladie de tay-sachs | rel=r_associated | relid=0 | w=20
  1141. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie de Tay-sachs
    n1=en:classical phenylketonuria | n2=maladie de Tay-sachs | rel=r_associated | relid=0 | w=20
  1142. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Maladie de Tay-Sachs
    n1=en:classical phenylketonuria | n2=Maladie de Tay-Sachs | rel=r_associated | relid=0 | w=20
  1143. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie de wolman
    n1=en:classical phenylketonuria | n2=maladie de wolman | rel=r_associated | relid=0 | w=20
  1144. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie de Wolman
    n1=en:classical phenylketonuria | n2=maladie de Wolman | rel=r_associated | relid=0 | w=20
  1145. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie des urines à l'odeur de sirop d'érable
    n1=en:classical phenylketonuria | n2=maladie des urines à l'odeur de sirop d'érable | rel=r_associated | relid=0 | w=20
  1146. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie des urines avec odeur de sirop erable
    n1=en:classical phenylketonuria | n2=maladie des urines avec odeur de sirop erable | rel=r_associated | relid=0 | w=20
  1147. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie du coeur
    n1=en:classical phenylketonuria | n2=maladie du coeur | rel=r_associated | relid=0 | w=20
  1148. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie du sirop d'érable
    n1=en:classical phenylketonuria | n2=maladie du sirop d'érable | rel=r_associated | relid=0 | w=20
  1149. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladie lysosomique de surcharge
    n1=en:classical phenylketonuria | n2=maladie lysosomique de surcharge | rel=r_associated | relid=0 | w=20
  1150. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladies cardiaques
    n1=en:classical phenylketonuria | n2=maladies cardiaques | rel=r_associated | relid=0 | w=20
  1151. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladies des bandes amniotiques
    n1=en:classical phenylketonuria | n2=maladies des bandes amniotiques | rel=r_associated | relid=0 | w=20
  1152. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> maladies du coeur
    n1=en:classical phenylketonuria | n2=maladies du coeur | rel=r_associated | relid=0 | w=20
  1153. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> malformation
    n1=en:classical phenylketonuria | n2=malformation | rel=r_associated | relid=0 | w=20
  1154. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> malformation congénitale
    n1=en:classical phenylketonuria | n2=malformation congénitale | rel=r_associated | relid=0 | w=20
  1155. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> mevalonic aciduria
    n1=en:classical phenylketonuria | n2=mevalonic aciduria | rel=r_associated | relid=0 | w=20
  1156. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> microalbuminurie
    n1=en:classical phenylketonuria | n2=microalbuminurie | rel=r_associated | relid=0 | w=20
  1157. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> mucolipidose II
    n1=en:classical phenylketonuria | n2=mucolipidose II | rel=r_associated | relid=0 | w=20
  1158. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> mucolipidose type ii
    n1=en:classical phenylketonuria | n2=mucolipidose type ii | rel=r_associated | relid=0 | w=20
  1159. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> mucolipidose type II
    n1=en:classical phenylketonuria | n2=mucolipidose type II | rel=r_associated | relid=0 | w=20
  1160. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> nanisme, retard mental, anomalies oculaires
    n1=en:classical phenylketonuria | n2=nanisme, retard mental, anomalies oculaires | rel=r_associated | relid=0 | w=20
  1161. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> neuro-acanthocytose
    n1=en:classical phenylketonuria | n2=neuro-acanthocytose | rel=r_associated | relid=0 | w=20
  1162. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> nystagmus congénital isolé
    n1=en:classical phenylketonuria | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
  1163. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> oligophrénie
    n1=en:classical phenylketonuria | n2=oligophrénie | rel=r_associated | relid=0 | w=20
  1164. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> omphalocèle
    n1=en:classical phenylketonuria | n2=omphalocèle | rel=r_associated | relid=0 | w=20
  1165. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> omphalocèles
    n1=en:classical phenylketonuria | n2=omphalocèles | rel=r_associated | relid=0 | w=20
  1166. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> otocéphale
    n1=en:classical phenylketonuria | n2=otocéphale | rel=r_associated | relid=0 | w=20
  1167. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> otocéphalie
    n1=en:classical phenylketonuria | n2=otocéphalie | rel=r_associated | relid=0 | w=20
  1168. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> oxalose
    n1=en:classical phenylketonuria | n2=oxalose | rel=r_associated | relid=0 | w=20
  1169. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> oxalose primitive
    n1=en:classical phenylketonuria | n2=oxalose primitive | rel=r_associated | relid=0 | w=20
  1170. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> oxaloses
    n1=en:classical phenylketonuria | n2=oxaloses | rel=r_associated | relid=0 | w=20
  1171. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> paridensité urinaire
    n1=en:classical phenylketonuria | n2=paridensité urinaire | rel=r_associated | relid=0 | w=20
  1172. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> pathologie congénitale
    n1=en:classical phenylketonuria | n2=pathologie congénitale | rel=r_associated | relid=0 | w=20
  1173. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> pathologie du coeur
    n1=en:classical phenylketonuria | n2=pathologie du coeur | rel=r_associated | relid=0 | w=20
  1174. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> peau sèche
    n1=en:classical phenylketonuria | n2=peau sèche | rel=r_associated | relid=0 | w=20
  1175. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> petite taille, hyperextensibilité, hernie et dépression oculaire
    n1=en:classical phenylketonuria | n2=petite taille, hyperextensibilité, hernie et dépression oculaire | rel=r_associated | relid=0 | w=20
  1176. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> phacomatose congenitale
    n1=en:classical phenylketonuria | n2=phacomatose congenitale | rel=r_associated | relid=0 | w=20
  1177. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> pied-bot
    n1=en:classical phenylketonuria | n2=pied-bot | rel=r_associated | relid=0 | w=20
  1178. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> polydipsie
    n1=en:classical phenylketonuria | n2=polydipsie | rel=r_associated | relid=0 | w=20
  1179. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> polyurie
    n1=en:classical phenylketonuria | n2=polyurie | rel=r_associated | relid=0 | w=20
  1180. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> progeria
    n1=en:classical phenylketonuria | n2=progeria | rel=r_associated | relid=0 | w=20
  1181. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> progéria
    n1=en:classical phenylketonuria | n2=progéria | rel=r_associated | relid=0 | w=20
  1182. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> protoproporphyrie érythropoïétique
    n1=en:classical phenylketonuria | n2=protoproporphyrie érythropoïétique | rel=r_associated | relid=0 | w=20
  1183. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> pseudo-hypoparathyroïdie
    n1=en:classical phenylketonuria | n2=pseudo-hypoparathyroïdie | rel=r_associated | relid=0 | w=20
  1184. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> pseudo-hypoparathyroïdisme
    n1=en:classical phenylketonuria | n2=pseudo-hypoparathyroïdisme | rel=r_associated | relid=0 | w=20
  1185. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> pseudohypoparathyroïdie
    n1=en:classical phenylketonuria | n2=pseudohypoparathyroïdie | rel=r_associated | relid=0 | w=20
  1186. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> pseudohypoparathyroïdisme
    n1=en:classical phenylketonuria | n2=pseudohypoparathyroïdisme | rel=r_associated | relid=0 | w=20
  1187. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> pterygium colli
    n1=en:classical phenylketonuria | n2=pterygium colli | rel=r_associated | relid=0 | w=20
  1188. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> puberté précoce
    n1=en:classical phenylketonuria | n2=puberté précoce | rel=r_associated | relid=0 | w=20
  1189. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Puberté précoce
    n1=en:classical phenylketonuria | n2=Puberté précoce | rel=r_associated | relid=0 | w=20
  1190. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> pyurie
    n1=en:classical phenylketonuria | n2=pyurie | rel=r_associated | relid=0 | w=20
  1191. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> retard mental
    n1=en:classical phenylketonuria | n2=retard mental | rel=r_associated | relid=0 | w=20
  1192. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Retard mental
    n1=en:classical phenylketonuria | n2=Retard mental | rel=r_associated | relid=0 | w=20
  1193. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> retard mental, retard de croissance, surdité, microgénitalisme lié au sexe
    n1=en:classical phenylketonuria | n2=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | rel=r_associated | relid=0 | w=20
  1194. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> retardation mentale
    n1=en:classical phenylketonuria | n2=retardation mentale | rel=r_associated | relid=0 | w=20
  1195. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> rétention des chylomicrons (maladie de la)
    n1=en:classical phenylketonuria | n2=rétention des chylomicrons (maladie de la) | rel=r_associated | relid=0 | w=20
  1196. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> sclérose tubéreuse du cerveau
    n1=en:classical phenylketonuria | n2=sclérose tubéreuse du cerveau | rel=r_associated | relid=0 | w=20
  1197. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Section 3-1 Maladies cardiaques
    n1=en:classical phenylketonuria | n2=Section 3-1 Maladies cardiaques | rel=r_associated | relid=0 | w=20
  1198. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> section 3-1 maladies cardiaques
    n1=en:classical phenylketonuria | n2=section 3-1 maladies cardiaques | rel=r_associated | relid=0 | w=20
  1199. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> semialdéhyde succinique-déshydrogénase (déficit en)
    n1=en:classical phenylketonuria | n2=semialdéhyde succinique-déshydrogénase (déficit en) | rel=r_associated | relid=0 | w=20
  1200. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> sirénomélie
    n1=en:classical phenylketonuria | n2=sirénomélie | rel=r_associated | relid=0 | w=20
  1201. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> sirop d'érable (urine à odeur de)
    n1=en:classical phenylketonuria | n2=sirop d'érable (urine à odeur de) | rel=r_associated | relid=0 | w=20
  1202. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> situs inversus
    n1=en:classical phenylketonuria | n2=situs inversus | rel=r_associated | relid=0 | w=20
  1203. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> situs mutatus
    n1=en:classical phenylketonuria | n2=situs mutatus | rel=r_associated | relid=0 | w=20
  1204. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> soif excessive
    n1=en:classical phenylketonuria | n2=soif excessive | rel=r_associated | relid=0 | w=20
  1205. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> sphingolipidose
    n1=en:classical phenylketonuria | n2=sphingolipidose | rel=r_associated | relid=0 | w=20
  1206. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> sténose du pylore
    n1=en:classical phenylketonuria | n2=sténose du pylore | rel=r_associated | relid=0 | w=20
  1207. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> sténose pylorique
    n1=en:classical phenylketonuria | n2=sténose pylorique | rel=r_associated | relid=0 | w=20
  1208. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Syndrome d'Angelman
    n1=en:classical phenylketonuria | n2=Syndrome d'Angelman | rel=r_associated | relid=0 | w=20
  1209. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome d'angelman
    n1=en:classical phenylketonuria | n2=syndrome d'angelman | rel=r_associated | relid=0 | w=20
  1210. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome d'Angelman
    n1=en:classical phenylketonuria | n2=syndrome d'Angelman | rel=r_associated | relid=0 | w=20
  1211. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de bride amniotique
    n1=en:classical phenylketonuria | n2=syndrome de bride amniotique | rel=r_associated | relid=0 | w=20
  1212. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de de Barsy
    n1=en:classical phenylketonuria | n2=syndrome de de Barsy | rel=r_associated | relid=0 | w=20
  1213. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de De Barsy
    n1=en:classical phenylketonuria | n2=syndrome de De Barsy | rel=r_associated | relid=0 | w=20
  1214. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de de barsy
    n1=en:classical phenylketonuria | n2=syndrome de de barsy | rel=r_associated | relid=0 | w=20
  1215. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de dubin-johnson
    n1=en:classical phenylketonuria | n2=syndrome de dubin-johnson | rel=r_associated | relid=0 | w=20
  1216. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de Dubin-Johnson
    n1=en:classical phenylketonuria | n2=syndrome de Dubin-Johnson | rel=r_associated | relid=0 | w=20
  1217. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de fragilité du chromosome X
    n1=en:classical phenylketonuria | n2=syndrome de fragilité du chromosome X | rel=r_associated | relid=0 | w=20
  1218. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de la marionnette joyeuse
    n1=en:classical phenylketonuria | n2=syndrome de la marionnette joyeuse | rel=r_associated | relid=0 | w=20
  1219. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de Laurence-Moon
    n1=en:classical phenylketonuria | n2=syndrome de Laurence-Moon | rel=r_associated | relid=0 | w=20
  1220. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de Lowe
    n1=en:classical phenylketonuria | n2=syndrome de Lowe | rel=r_associated | relid=0 | w=20
  1221. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de Martin-Bell
    n1=en:classical phenylketonuria | n2=syndrome de Martin-Bell | rel=r_associated | relid=0 | w=20
  1222. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de Rett
    n1=en:classical phenylketonuria | n2=syndrome de Rett | rel=r_associated | relid=0 | w=20
  1223. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de rett
    n1=en:classical phenylketonuria | n2=syndrome de rett | rel=r_associated | relid=0 | w=20
  1224. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Syndrome de Rett
    n1=en:classical phenylketonuria | n2=Syndrome de Rett | rel=r_associated | relid=0 | w=20
  1225. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de synostose spondylo-carpo-tarsale
    n1=en:classical phenylketonuria | n2=syndrome de synostose spondylo-carpo-tarsale | rel=r_associated | relid=0 | w=20
  1226. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome de Zellweger
    n1=en:classical phenylketonuria | n2=syndrome de Zellweger | rel=r_associated | relid=0 | w=20
  1227. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome des brides amniotiques
    n1=en:classical phenylketonuria | n2=syndrome des brides amniotiques | rel=r_associated | relid=0 | w=20
  1228. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome progéroïde de De Barsy
    n1=en:classical phenylketonuria | n2=syndrome progéroïde de De Barsy | rel=r_associated | relid=0 | w=20
  1229. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome progéroïde de de barsy
    n1=en:classical phenylketonuria | n2=syndrome progéroïde de de barsy | rel=r_associated | relid=0 | w=20
  1230. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome tricho-rhino-phalangien de type 2
    n1=en:classical phenylketonuria | n2=syndrome tricho-rhino-phalangien de type 2 | rel=r_associated | relid=0 | w=20
  1231. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome tricho-rhino-phalangien de type ii
    n1=en:classical phenylketonuria | n2=syndrome tricho-rhino-phalangien de type ii | rel=r_associated | relid=0 | w=20
  1232. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> syndrome tricho-rhino-phalangien de type II
    n1=en:classical phenylketonuria | n2=syndrome tricho-rhino-phalangien de type II | rel=r_associated | relid=0 | w=20
  1233. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> tare congénitale
    n1=en:classical phenylketonuria | n2=tare congénitale | rel=r_associated | relid=0 | w=20
  1234. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> télécanthus
    n1=en:classical phenylketonuria | n2=télécanthus | rel=r_associated | relid=0 | w=20
  1235. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> télécanthus-hypertélorisme-strabisme (syndrome)
    n1=en:classical phenylketonuria | n2=télécanthus-hypertélorisme-strabisme (syndrome) | rel=r_associated | relid=0 | w=20
  1236. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> température corporelle élevée
    n1=en:classical phenylketonuria | n2=température corporelle élevée | rel=r_associated | relid=0 | w=20
  1237. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> tétralogie de Fallot
    n1=en:classical phenylketonuria | n2=tétralogie de Fallot | rel=r_associated | relid=0 | w=20
  1238. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> tétralogie de fallot
    n1=en:classical phenylketonuria | n2=tétralogie de fallot | rel=r_associated | relid=0 | w=20
  1239. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> TPN ou NADP
    n1=en:classical phenylketonuria | n2=TPN ou NADP | rel=r_associated | relid=0 | w=20
  1240. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Trouble anxieux
    n1=en:classical phenylketonuria | n2=Trouble anxieux | rel=r_associated | relid=0 | w=20
  1241. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> trouble anxieux
    n1=en:classical phenylketonuria | n2=trouble anxieux | rel=r_associated | relid=0 | w=20
  1242. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> trouble cardiaque
    n1=en:classical phenylketonuria | n2=trouble cardiaque | rel=r_associated | relid=0 | w=20
  1243. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> trouble chromosomique
    n1=en:classical phenylketonuria | n2=trouble chromosomique | rel=r_associated | relid=0 | w=20
  1244. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> trouble métabolique transitoire des acides aminés
    n1=en:classical phenylketonuria | n2=trouble métabolique transitoire des acides aminés | rel=r_associated | relid=0 | w=20
  1245. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> troubles endocriniens, épilepsie et déficience mentale
    n1=en:classical phenylketonuria | n2=troubles endocriniens, épilepsie et déficience mentale | rel=r_associated | relid=0 | w=20
  1246. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> tubulopathie rénale, diabète sucré, ataxie cérébelleuse secondaire à une duplication de l'ADN mitochondrial
    n1=en:classical phenylketonuria | n2=tubulopathie rénale, diabète sucré, ataxie cérébelleuse secondaire à une duplication de l'ADN mitochondrial | rel=r_associated | relid=0 | w=20
  1247. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> urétérocèle
    n1=en:classical phenylketonuria | n2=urétérocèle | rel=r_associated | relid=0 | w=20
  1248. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> van Bogaert (xanthomatose cérébrotendineuse de)
    n1=en:classical phenylketonuria | n2=van Bogaert (xanthomatose cérébrotendineuse de) | rel=r_associated | relid=0 | w=20
  1249. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> ventriculomégalie cérébrale
    n1=en:classical phenylketonuria | n2=ventriculomégalie cérébrale | rel=r_associated | relid=0 | w=20
  1250. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> vice de conformation
    n1=en:classical phenylketonuria | n2=vice de conformation | rel=r_associated | relid=0 | w=20
  1251. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Walker-Warburg (syndrome de)
    n1=en:classical phenylketonuria | n2=Walker-Warburg (syndrome de) | rel=r_associated | relid=0 | w=20
  1252. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Wolman (maladie de)
    n1=en:classical phenylketonuria | n2=Wolman (maladie de) | rel=r_associated | relid=0 | w=20
  1253. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> xanthomatose cérébro-tendineuse
    n1=en:classical phenylketonuria | n2=xanthomatose cérébro-tendineuse | rel=r_associated | relid=0 | w=20
  1254. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse
    n1=en:classical phenylketonuria | n2=xanthomatose cérébrotendineuse | rel=r_associated | relid=0 | w=20
  1255. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse de Van Bogaert
    n1=en:classical phenylketonuria | n2=xanthomatose cérébrotendineuse de Van Bogaert | rel=r_associated | relid=0 | w=20
  1256. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> xeroderma pigmentosum
    n1=en:classical phenylketonuria | n2=xeroderma pigmentosum | rel=r_associated | relid=0 | w=20
  1257. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> Xeroderma pigmentosum
    n1=en:classical phenylketonuria | n2=Xeroderma pigmentosum | rel=r_associated | relid=0 | w=20
  1258. en:classical phenylketonuria -- r_associated #0: 20 / 0.465 -> xérodermite pigmentaire
    n1=en:classical phenylketonuria | n2=xérodermite pigmentaire | rel=r_associated | relid=0 | w=20
≈ 1880 relations entrantes

  1. en:maple syrup urine disease --- r_associated #0: 697 --> en:classical phenylketonuria
    n1=en:maple syrup urine disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=697
  2. leucinose --- r_associated #0: 598.82 --> en:classical phenylketonuria
    n1=leucinose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=598.82
  3. maladie du sirop d'érable --- r_associated #0: 594.46 --> en:classical phenylketonuria
    n1=maladie du sirop d'érable | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=594.46
  4. en:branched-chain ketoaciduria --- r_associated #0: 520 --> en:classical phenylketonuria
    n1=en:branched-chain ketoaciduria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=520
  5. fièvre
    (médecine)
     --- r_associated #0: 444 --> en:classical phenylketonuria
    n1=fièvre
    (médecine)
    | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=444
  6. en:fever --- r_associated #0: 440 --> en:classical phenylketonuria
    n1=en:fever | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=440
  7. anomalie congénitale --- r_associated #0: 424 --> en:classical phenylketonuria
    n1=anomalie congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=424
  8. en:congenital abnormality --- r_associated #0: 423 --> en:classical phenylketonuria
    n1=en:congenital abnormality | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=423
  9. maladie héréditaire --- r_associated #0: 391 --> en:classical phenylketonuria
    n1=maladie héréditaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=391
  10. en:hereditary disease --- r_associated #0: 390 --> en:classical phenylketonuria
    n1=en:hereditary disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=390
  11. maladie génétique --- r_associated #0: 386 --> en:classical phenylketonuria
    n1=maladie génétique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=386
  12. maladie du coeur --- r_associated #0: 365 --> en:classical phenylketonuria
    n1=maladie du coeur | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=365
  13. en:heart disorder --- r_associated #0: 360 --> en:classical phenylketonuria
    n1=en:heart disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=360
  14. maladie cardiaque non précisée --- r_associated #0: 360 --> en:classical phenylketonuria
    n1=maladie cardiaque non précisée | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=360
  15. anomalie cardiaque --- r_associated #0: 356 --> en:classical phenylketonuria
    n1=anomalie cardiaque | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=356
  16. malformation congénitale --- r_associated #0: 356 --> en:classical phenylketonuria
    n1=malformation congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=356
  17. en:congenital anomaly --- r_associated #0: 355 --> en:classical phenylketonuria
    n1=en:congenital anomaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=355
  18. en:genetic disease --- r_associated #0: 355 --> en:classical phenylketonuria
    n1=en:genetic disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=355
  19. card --- r_associated #0: 350 --> en:classical phenylketonuria
    n1=card | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=350
  20. affection cardiaque --- r_associated #0: 345 --> en:classical phenylketonuria
    n1=affection cardiaque | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=345
  21. en:heart malformation --- r_associated #0: 341 --> en:classical phenylketonuria
    n1=en:heart malformation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=341
  22. anomalie du coeur --- r_associated #0: 340 --> en:classical phenylketonuria
    n1=anomalie du coeur | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=340
  23. malformation cardiaque --- r_associated #0: 339 --> en:classical phenylketonuria
    n1=malformation cardiaque | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=339
  24. maladie cardiaque --- r_associated #0: 335 --> en:classical phenylketonuria
    n1=maladie cardiaque | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=335
  25. trouble cardiaque --- r_associated #0: 335 --> en:classical phenylketonuria
    n1=trouble cardiaque | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=335
  26. cardiopathie --- r_associated #0: 325 --> en:classical phenylketonuria
    n1=cardiopathie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=325
  27. en:heart diseases --- r_associated #0: 325 --> en:classical phenylketonuria
    n1=en:heart diseases | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=325
  28. pathologie du coeur --- r_associated #0: 325 --> en:classical phenylketonuria
    n1=pathologie du coeur | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=325
  29. anormalité des chromosomes --- r_associated #0: 321 --> en:classical phenylketonuria
    n1=anormalité des chromosomes | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=321
  30. omphalocèle --- r_associated #0: 321 --> en:classical phenylketonuria
    n1=omphalocèle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=321
  31. en:chromosome disorder --- r_associated #0: 320 --> en:classical phenylketonuria
    n1=en:chromosome disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=320
  32. en:omphalocele --- r_associated #0: 317 --> en:classical phenylketonuria
    n1=en:omphalocele | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=317
  33. hernie ombilicale congénitale --- r_associated #0: 315 --> en:classical phenylketonuria
    n1=hernie ombilicale congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=315
  34. en:congenital defect --- r_associated #0: 310 --> en:classical phenylketonuria
    n1=en:congenital defect | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=310
  35. exomphale --- r_associated #0: 310 --> en:classical phenylketonuria
    n1=exomphale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=310
  36. exomphale congénitale --- r_associated #0: 310 --> en:classical phenylketonuria
    n1=exomphale congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=310
  37. section 3-1 maladies cardiaques --- r_associated #0: 310 --> en:classical phenylketonuria
    n1=section 3-1 maladies cardiaques | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=310
  38. omphalocèles --- r_associated #0: 306 --> en:classical phenylketonuria
    n1=omphalocèles | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=306
  39. en:genetic disorder --- r_associated #0: 305 --> en:classical phenylketonuria
    n1=en:genetic disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=305
  40. hernie ombilicale --- r_associated #0: 305 --> en:classical phenylketonuria
    n1=hernie ombilicale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=305
  41. en:umbilical hernia --- r_associated #0: 300 --> en:classical phenylketonuria
    n1=en:umbilical hernia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=300
  42. déformation congénitale --- r_associated #0: 296 --> en:classical phenylketonuria
    n1=déformation congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=296
  43. déficience congénitale --- r_associated #0: 295 --> en:classical phenylketonuria
    n1=déficience congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=295
  44. hernies ombilicales --- r_associated #0: 291 --> en:classical phenylketonuria
    n1=hernies ombilicales | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=291
  45. anomalie héréditaire --- r_associated #0: 281 --> en:classical phenylketonuria
    n1=anomalie héréditaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=281
  46. en:classical maple syrup urine disease --- r_associated #0: 280 --> en:classical phenylketonuria
    n1=en:classical maple syrup urine disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=280
  47. en:thiamin-responsive maple syrup urine disease --- r_associated #0: 280 --> en:classical phenylketonuria
    n1=en:thiamin-responsive maple syrup urine disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=280
  48. déficit en céto-acide décarboxylase --- r_associated #0: 275 --> en:classical phenylketonuria
    n1=déficit en céto-acide décarboxylase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=275
  49. maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 275 --> en:classical phenylketonuria
    n1=maladie des urines à l'odeur de sirop d'érable | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=275
  50. maladie des urines avec odeur de sirop erable --- r_associated #0: 270 --> en:classical phenylketonuria
    n1=maladie des urines avec odeur de sirop erable | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=270
  51. en:craniosynostosis --- r_associated #0: 268 --> en:classical phenylketonuria
    n1=en:craniosynostosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=268
  52. crâniosynostose --- r_associated #0: 266 --> en:classical phenylketonuria
    n1=crâniosynostose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=266
  53. crânio-sténose --- r_associated #0: 265 --> en:classical phenylketonuria
    n1=crânio-sténose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=265
  54. crâniosténose --- r_associated #0: 265 --> en:classical phenylketonuria
    n1=crâniosténose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=265
  55. craniosynostose --- r_associated #0: 255 --> en:classical phenylketonuria
    n1=craniosynostose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=255
  56. trouble chromosomique --- r_associated #0: 250 --> en:classical phenylketonuria
    n1=trouble chromosomique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=250
  57. anomalie chromosomique --- r_associated #0: 242 --> en:classical phenylketonuria
    n1=anomalie chromosomique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=242
  58. maladies cardiaques --- r_associated #0: 240 --> en:classical phenylketonuria
    n1=maladies cardiaques | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=240
  59. danse de saint Guy --- r_associated #0: 235 --> en:classical phenylketonuria
    n1=danse de saint Guy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=235
  60. chorées --- r_associated #0: 230 --> en:classical phenylketonuria
    n1=chorées | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=230
  61. en:rheumatic chorea --- r_associated #0: 226 --> en:classical phenylketonuria
    n1=en:rheumatic chorea | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=226
  62. cardiopathies --- r_associated #0: 225 --> en:classical phenylketonuria
    n1=cardiopathies | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=225
  63. chorée rhumatismale --- r_associated #0: 225 --> en:classical phenylketonuria
    n1=chorée rhumatismale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=225
  64. maladies du coeur --- r_associated #0: 225 --> en:classical phenylketonuria
    n1=maladies du coeur | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=225
  65. exstrophie --- r_associated #0: 220 --> en:classical phenylketonuria
    n1=exstrophie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=220
  66. en:exstrophy --- r_associated #0: 216 --> en:classical phenylketonuria
    n1=en:exstrophy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=216
  67. chorée de saint jean --- r_associated #0: 215 --> en:classical phenylketonuria
    n1=chorée de saint jean | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=215
  68. chorée rhumatismale sans atteinte cardiaque --- r_associated #0: 215 --> en:classical phenylketonuria
    n1=chorée rhumatismale sans atteinte cardiaque | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=215
  69. affections cardiaques --- r_associated #0: 210 --> en:classical phenylketonuria
    n1=affections cardiaques | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=210
  70. chorée héréditaire --- r_associated #0: 210 --> en:classical phenylketonuria
    n1=chorée héréditaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=210
  71. en:genetic condition --- r_associated #0: 210 --> en:classical phenylketonuria
    n1=en:genetic condition | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=210
  72. anomalie congénitale de l'oeil --- r_associated #0: 209 --> en:classical phenylketonuria
    n1=anomalie congénitale de l'oeil | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=209
  73. Chorée --- r_associated #0: 206 --> en:classical phenylketonuria
    n1=Chorée | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=206
  74. en:congenital eye disorder --- r_associated #0: 205 --> en:classical phenylketonuria
    n1=en:congenital eye disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=205
  75. en:huntington's disease --- r_associated #0: 204 --> en:classical phenylketonuria
    n1=en:huntington's disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=204
  76. chorée de Huntington --- r_associated #0: 202 --> en:classical phenylketonuria
    n1=chorée de Huntington | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=202
  77. difformité congénitale --- r_associated #0: 200 --> en:classical phenylketonuria
    n1=difformité congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=200
  78. en:infantile hypophosphatasia --- r_associated #0: 197 --> en:classical phenylketonuria
    n1=en:infantile hypophosphatasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=197
  79. maladie de Huntington --- r_associated #0: 197 --> en:classical phenylketonuria
    n1=maladie de Huntington | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=197
  80. hypophosphatasie foetale --- r_associated #0: 196 --> en:classical phenylketonuria
    n1=hypophosphatasie foetale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=196
  81. hypophosphatasie infantile --- r_associated #0: 196 --> en:classical phenylketonuria
    n1=hypophosphatasie infantile | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=196
  82. chorée de Sydenham --- r_associated #0: 195 --> en:classical phenylketonuria
    n1=chorée de Sydenham | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=195
  83. maladie congénitale --- r_associated #0: 190 --> en:classical phenylketonuria
    n1=maladie congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=190
  84. hypoplasie --- r_associated #0: 187 --> en:classical phenylketonuria
    n1=hypoplasie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=187
  85. craniosténose --- r_associated #0: 185 --> en:classical phenylketonuria
    n1=craniosténose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=185
  86. en:hypoplasia --- r_associated #0: 185 --> en:classical phenylketonuria
    n1=en:hypoplasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=185
  87. pathologie congénitale --- r_associated #0: 185 --> en:classical phenylketonuria
    n1=pathologie congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=185
  88. affection oculaire congénitale --- r_associated #0: 180 --> en:classical phenylketonuria
    n1=affection oculaire congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=180
  89. en:walker-warburg syndrome --- r_associated #0: 180 --> en:classical phenylketonuria
    n1=en:walker-warburg syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=180
  90. syndrome de Walker-Warburg --- r_associated #0: 178 --> en:classical phenylketonuria
    n1=syndrome de Walker-Warburg | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=178
  91. en:chromosomal abnormality --- r_associated #0: 175 --> en:classical phenylketonuria
    n1=en:chromosomal abnormality | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=175
  92. en:heart disease --- r_associated #0: 175 --> en:classical phenylketonuria
    n1=en:heart disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=175
  93. en:pyruvate carboxylase deficiency --- r_associated #0: 175 --> en:classical phenylketonuria
    n1=en:pyruvate carboxylase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=175
  94. déficit en pyruvate carboxylase --- r_associated #0: 174 --> en:classical phenylketonuria
    n1=déficit en pyruvate carboxylase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=174
  95. en:card --- r_associated #0: 170 --> en:classical phenylketonuria
    n1=en:card | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=170
  96. en:xeroderma pigmentosum --- r_associated #0: 169 --> en:classical phenylketonuria
    n1=en:xeroderma pigmentosum | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=169
  97. xeroderma pigmentosum --- r_associated #0: 168 --> en:classical phenylketonuria
    n1=xeroderma pigmentosum | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=168
  98. en:zellweger syndrome --- r_associated #0: 167 --> en:classical phenylketonuria
    n1=en:zellweger syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=167
  99. en:Zellweger syndrome --- r_associated #0: 165 --> en:classical phenylketonuria
    n1=en:Zellweger syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=165
  100. en:wolman disease --- r_associated #0: 163 --> en:classical phenylketonuria
    n1=en:wolman disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=163
  101. maladie de Wolman --- r_associated #0: 161 --> en:classical phenylketonuria
    n1=maladie de Wolman | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=161
  102. hyperoxalurie primitive --- r_associated #0: 160 --> en:classical phenylketonuria
    n1=hyperoxalurie primitive | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=160
  103. en:primary hyperoxaluria --- r_associated #0: 158 --> en:classical phenylketonuria
    n1=en:primary hyperoxaluria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=158
  104. hyperoxalurie primaire --- r_associated #0: 151 --> en:classical phenylketonuria
    n1=hyperoxalurie primaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=151
  105. oxaloses --- r_associated #0: 151 --> en:classical phenylketonuria
    n1=oxaloses | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=151
  106. oxalose primitive --- r_associated #0: 146 --> en:classical phenylketonuria
    n1=oxalose primitive | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=146
  107. oxalose --- r_associated #0: 140 --> en:classical phenylketonuria
    n1=oxalose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=140
  108. en:angelman syndrome --- r_associated #0: 131 --> en:classical phenylketonuria
    n1=en:angelman syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=131
  109. hypertriglycéridémie --- r_associated #0: 131 --> en:classical phenylketonuria
    n1=hypertriglycéridémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=131
  110. Retard mental --- r_associated #0: 130 --> en:classical phenylketonuria
    n1=Retard mental | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=130
  111. en:congenital malformation --- r_associated #0: 130 --> en:classical phenylketonuria
    n1=en:congenital malformation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=130
  112. retard mental --- r_associated #0: 130 --> en:classical phenylketonuria
    n1=retard mental | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=130
  113. syndrome d'Angelman --- r_associated #0: 130 --> en:classical phenylketonuria
    n1=syndrome d'Angelman | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=130
  114. en:mental retardation --- r_associated #0: 128 --> en:classical phenylketonuria
    n1=en:mental retardation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=128
  115. en:hypertriglyceridemia --- r_associated #0: 127 --> en:classical phenylketonuria
    n1=en:hypertriglyceridemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=127
  116. retardation mentale --- r_associated #0: 126 --> en:classical phenylketonuria
    n1=retardation mentale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=126
  117. gout --- r_associated #0: 122 --> en:classical phenylketonuria
    n1=gout | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=122
  118. situs inversus --- r_associated #0: 122 --> en:classical phenylketonuria
    n1=situs inversus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=122
  119. en:birth defect --- r_associated #0: 120 --> en:classical phenylketonuria
    n1=en:birth defect | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=120
  120. en:situs inversus --- r_associated #0: 118 --> en:classical phenylketonuria
    n1=en:situs inversus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=118
  121. ancyloglosse --- r_associated #0: 111 --> en:classical phenylketonuria
    n1=ancyloglosse | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=111
  122. ankyloglosse --- r_associated #0: 111 --> en:classical phenylketonuria
    n1=ankyloglosse | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=111
  123. en:genetic illness --- r_associated #0: 110 --> en:classical phenylketonuria
    n1=en:genetic illness | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=110
  124. en:ankyloglossia --- r_associated #0: 109 --> en:classical phenylketonuria
    n1=en:ankyloglossia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=109
  125. tétralogie de fallot --- r_associated #0: 106 --> en:classical phenylketonuria
    n1=tétralogie de fallot | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=106
  126. en:tetralogy of fallot --- r_associated #0: 103 --> en:classical phenylketonuria
    n1=en:tetralogy of fallot | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=103
  127. en:anterior plagiocephalies, synostotic --- r_associated #0: 102 --> en:classical phenylketonuria
    n1=en:anterior plagiocephalies, synostotic | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=102
  128. otocéphalie --- r_associated #0: 101 --> en:classical phenylketonuria
    n1=otocéphalie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=101
  129. syndrome des brides amniotiques --- r_associated #0: 101 --> en:classical phenylketonuria
    n1=syndrome des brides amniotiques | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=101
  130. syndrome de Rett --- r_associated #0: 100 --> en:classical phenylketonuria
    n1=syndrome de Rett | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=100
  131. tétralogie de Fallot --- r_associated #0: 100 --> en:classical phenylketonuria
    n1=tétralogie de Fallot | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=100
  132. en:glutaric acidemia type 1 --- r_associated #0: 99 --> en:classical phenylketonuria
    n1=en:glutaric acidemia type 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=99
  133. en:amniotic band syndrome --- r_associated #0: 98 --> en:classical phenylketonuria
    n1=en:amniotic band syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=98
  134. en:otocephaly --- r_associated #0: 98 --> en:classical phenylketonuria
    n1=en:otocephaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=98
  135. en:rett syndrome --- r_associated #0: 98 --> en:classical phenylketonuria
    n1=en:rett syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=98
  136. exencéphalie --- r_associated #0: 97 --> en:classical phenylketonuria
    n1=exencéphalie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=97
  137. acidurie glutarique de type 1 --- r_associated #0: 96 --> en:classical phenylketonuria
    n1=acidurie glutarique de type 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=96
  138. hypertélorisme --- r_associated #0: 96 --> en:classical phenylketonuria
    n1=hypertélorisme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=96
  139. maladies des bandes amniotiques --- r_associated #0: 96 --> en:classical phenylketonuria
    n1=maladies des bandes amniotiques | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=96
  140. en:exencephaly --- r_associated #0: 95 --> en:classical phenylketonuria
    n1=en:exencephaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=95
  141. en:tetralogy of Fallot --- r_associated #0: 95 --> en:classical phenylketonuria
    n1=en:tetralogy of Fallot | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=95
  142. hyperplasie congénitale des surrénales --- r_associated #0: 95 --> en:classical phenylketonuria
    n1=hyperplasie congénitale des surrénales | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=95
  143. en:hypertelorism --- r_associated #0: 92 --> en:classical phenylketonuria
    n1=en:hypertelorism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=92
  144. acidémie glutarique de type 1 --- r_associated #0: 91 --> en:classical phenylketonuria
    n1=acidémie glutarique de type 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=91
  145. en:congenital adrenal hyperplasia --- r_associated #0: 91 --> en:classical phenylketonuria
    n1=en:congenital adrenal hyperplasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=91
  146. syndrome de bride amniotique --- r_associated #0: 91 --> en:classical phenylketonuria
    n1=syndrome de bride amniotique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=91
  147. en:Angelman syndrome --- r_associated #0: 90 --> en:classical phenylketonuria
    n1=en:Angelman syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=90
  148. en:Huntington's disease --- r_associated #0: 90 --> en:classical phenylketonuria
    n1=en:Huntington's disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=90
  149. en:Umbilical hernia --- r_associated #0: 90 --> en:classical phenylketonuria
    n1=en:Umbilical hernia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=90
  150. progeria --- r_associated #0: 90 --> en:classical phenylketonuria
    n1=progeria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=90
  151. soif excessive --- r_associated #0: 90 --> en:classical phenylketonuria
    n1=soif excessive | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=90
  152. en:progeria --- r_associated #0: 86 --> en:classical phenylketonuria
    n1=en:progeria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=86
  153. hydrocéphalie --- r_associated #0: 86 --> en:classical phenylketonuria
    n1=hydrocéphalie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=86
  154. hyperthermie --- r_associated #0: 86 --> en:classical phenylketonuria
    n1=hyperthermie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=86
  155. Section 3-1 Maladies cardiaques --- r_associated #0: 85 --> en:classical phenylketonuria
    n1=Section 3-1 Maladies cardiaques | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=85
  156. en:mevalonic aciduria --- r_associated #0: 85 --> en:classical phenylketonuria
    n1=en:mevalonic aciduria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=85
  157. en:tetralogy --- r_associated #0: 85 --> en:classical phenylketonuria
    n1=en:tetralogy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=85
  158. en:ventriculomeglia --- r_associated #0: 85 --> en:classical phenylketonuria
    n1=en:ventriculomeglia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=85
  159. tare congénitale --- r_associated #0: 85 --> en:classical phenylketonuria
    n1=tare congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=85
  160. trouble anxieux --- r_associated #0: 85 --> en:classical phenylketonuria
    n1=trouble anxieux | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=85
  161. progéria --- r_associated #0: 84 --> en:classical phenylketonuria
    n1=progéria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=84
  162. en:anxiety disorder --- r_associated #0: 83 --> en:classical phenylketonuria
    n1=en:anxiety disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=83
  163. en:cerebral ventriculomegaly --- r_associated #0: 83 --> en:classical phenylketonuria
    n1=en:cerebral ventriculomegaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=83
  164. mevalonic aciduria --- r_associated #0: 82 --> en:classical phenylketonuria
    n1=mevalonic aciduria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=82
  165. en:polydipsia --- r_associated #0: 81 --> en:classical phenylketonuria
    n1=en:polydipsia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=81
  166. laparoschisis --- r_associated #0: 81 --> en:classical phenylketonuria
    n1=laparoschisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=81
  167. en:Fallot's disease --- r_associated #0: 80 --> en:classical phenylketonuria
    n1=en:Fallot's disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=80
  168. sclérose tubéreuse du cerveau --- r_associated #0: 80 --> en:classical phenylketonuria
    n1=sclérose tubéreuse du cerveau | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=80
  169. ventriculomégalie cérébrale --- r_associated #0: 80 --> en:classical phenylketonuria
    n1=ventriculomégalie cérébrale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=80
  170. en:gastroschisis --- r_associated #0: 79 --> en:classical phenylketonuria
    n1=en:gastroschisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=79
  171. en:tuberous sclerosis --- r_associated #0: 79 --> en:classical phenylketonuria
    n1=en:tuberous sclerosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=79
  172. syndrome tricho-rhino-phalangien de type ii --- r_associated #0: 78 --> en:classical phenylketonuria
    n1=syndrome tricho-rhino-phalangien de type ii | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=78
  173. polydipsie --- r_associated #0: 77 --> en:classical phenylketonuria
    n1=polydipsie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=77
  174. goutte
    (maladie)
     --- r_associated #0: 76 --> en:classical phenylketonuria
    n1=goutte
    (maladie)
    | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=76
  175. syndrome tricho-rhino-phalangien de type 2 --- r_associated #0: 76 --> en:classical phenylketonuria
    n1=syndrome tricho-rhino-phalangien de type 2 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=76
  176. diabète sucré --- r_associated #0: 75 --> en:classical phenylketonuria
    n1=diabète sucré | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=75
  177. en:gout --- r_associated #0: 75 --> en:classical phenylketonuria
    n1=en:gout | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=75
  178. en:sugar diabetes --- r_associated #0: 75 --> en:classical phenylketonuria
    n1=en:sugar diabetes | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=75
  179. élévation de la température corporelle --- r_associated #0: 75 --> en:classical phenylketonuria
    n1=élévation de la température corporelle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=75
  180. en:diabetes mellitus --- r_associated #0: 74 --> en:classical phenylketonuria
    n1=en:diabetes mellitus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=74
  181. gastroschisis --- r_associated #0: 74 --> en:classical phenylketonuria
    n1=gastroschisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=74
  182. en:fragile x syndrome --- r_associated #0: 72 --> en:classical phenylketonuria
    n1=en:fragile x syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=72
  183. en:ectopia cordis --- r_associated #0: 71 --> en:classical phenylketonuria
    n1=en:ectopia cordis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=71
  184. en:hyperthermia --- r_associated #0: 71 --> en:classical phenylketonuria
    n1=en:hyperthermia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=71
  185. en:trichorhinophalangeal syndrome type ii --- r_associated #0: 71 --> en:classical phenylketonuria
    n1=en:trichorhinophalangeal syndrome type ii | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=71
  186. Syndrome d'Angelman --- r_associated #0: 70 --> en:classical phenylketonuria
    n1=Syndrome d'Angelman | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=70
  187. ectopia cordis --- r_associated #0: 70 --> en:classical phenylketonuria
    n1=ectopia cordis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=70
  188. en:fragile X syndrome --- r_associated #0: 70 --> en:classical phenylketonuria
    n1=en:fragile X syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=70
  189. sœurs siamoises --- r_associated #0: 70 --> en:classical phenylketonuria
    n1=sœurs siamoises | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=70
  190. en:Klinefelter syndrome --- r_associated #0: 68 --> en:classical phenylketonuria
    n1=en:Klinefelter syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=68
  191. en:atrial septal defect --- r_associated #0: 67 --> en:classical phenylketonuria
    n1=en:atrial septal defect | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=67
  192. en:klinefelter syndrome --- r_associated #0: 67 --> en:classical phenylketonuria
    n1=en:klinefelter syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=67
  193. arriération mentale --- r_associated #0: 66 --> en:classical phenylketonuria
    n1=arriération mentale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=66
  194. débilité mentale --- r_associated #0: 66 --> en:classical phenylketonuria
    n1=débilité mentale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=66
  195. fente labiale --- r_associated #0: 66 --> en:classical phenylketonuria
    n1=fente labiale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=66
  196. soeurs siamoises --- r_associated #0: 66 --> en:classical phenylketonuria
    n1=soeurs siamoises | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=66
  197. Syndrome de Rett --- r_associated #0: 65 --> en:classical phenylketonuria
    n1=Syndrome de Rett | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=65
  198. anomalie du septum auriculaire --- r_associated #0: 65 --> en:classical phenylketonuria
    n1=anomalie du septum auriculaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=65
  199. en:excessive thirst --- r_associated #0: 65 --> en:classical phenylketonuria
    n1=en:excessive thirst | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=65
  200. en:labial fissure --- r_associated #0: 65 --> en:classical phenylketonuria
    n1=en:labial fissure | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=65
  201. fente labiopalatine et blépharophimosis --- r_associated #0: 65 --> en:classical phenylketonuria
    n1=fente labiopalatine et blépharophimosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=65
  202. kératocône postérieur-fente labiale-petite taille --- r_associated #0: 65 --> en:classical phenylketonuria
    n1=kératocône postérieur-fente labiale-petite taille | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=65
  203. maladie du cœur --- r_associated #0: 65 --> en:classical phenylketonuria
    n1=maladie du cœur | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=65
  204. peau sèche --- r_associated #0: 65 --> en:classical phenylketonuria
    n1=peau sèche | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=65
  205. syndrome de de barsy --- r_associated #0: 65 --> en:classical phenylketonuria
    n1=syndrome de de barsy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=65
  206. syndrome de fragilité du chromosome X --- r_associated #0: 65 --> en:classical phenylketonuria
    n1=syndrome de fragilité du chromosome X | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=65
  207. congénitale --- r_associated #0: 64 --> en:classical phenylketonuria
    n1=congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=64
  208. cyclopia --- r_associated #0: 64 --> en:classical phenylketonuria
    n1=cyclopia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=64
  209. en:cleft lip --- r_associated #0: 64 --> en:classical phenylketonuria
    n1=en:cleft lip | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=64
  210. en:cyclopia --- r_associated #0: 64 --> en:classical phenylketonuria
    n1=en:cyclopia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=64
  211. en:i-cell disease --- r_associated #0: 64 --> en:classical phenylketonuria
    n1=en:i-cell disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=64
  212. urétérocèle --- r_associated #0: 64 --> en:classical phenylketonuria
    n1=urétérocèle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=64
  213. en:de sanctis-cacchione syndrome --- r_associated #0: 63 --> en:classical phenylketonuria
    n1=en:de sanctis-cacchione syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=63
  214. syndrome d'angelman --- r_associated #0: 63 --> en:classical phenylketonuria
    n1=syndrome d'angelman | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=63
  215. cyclopie --- r_associated #0: 62 --> en:classical phenylketonuria
    n1=cyclopie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=62
  216. en:congenital --- r_associated #0: 61 --> en:classical phenylketonuria
    n1=en:congenital | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=61
  217. en:dry skin --- r_associated #0: 61 --> en:classical phenylketonuria
    n1=en:dry skin | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=61
  218. en:dubin-johnson syndrome --- r_associated #0: 61 --> en:classical phenylketonuria
    n1=en:dubin-johnson syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=61
  219. hyperlipidémie --- r_associated #0: 61 --> en:classical phenylketonuria
    n1=hyperlipidémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=61
  220. syndrome de De Barsy --- r_associated #0: 61 --> en:classical phenylketonuria
    n1=syndrome de De Barsy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=61
  221. syndrome progéroïde de De Barsy --- r_associated #0: 61 --> en:classical phenylketonuria
    n1=syndrome progéroïde de De Barsy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=61
  222. anomalie cytogénétique --- r_associated #0: 60 --> en:classical phenylketonuria
    n1=anomalie cytogénétique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=60
  223. en:I-cell disease --- r_associated #0: 60 --> en:classical phenylketonuria
    n1=en:I-cell disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=60
  224. en:cardiac diseases --- r_associated #0: 60 --> en:classical phenylketonuria
    n1=en:cardiac diseases | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=60
  225. en:hyperlipidaemia --- r_associated #0: 60 --> en:classical phenylketonuria
    n1=en:hyperlipidaemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=60
  226. en:ureterocele --- r_associated #0: 60 --> en:classical phenylketonuria
    n1=en:ureterocele | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=60
  227. idiotie xérodermique --- r_associated #0: 60 --> en:classical phenylketonuria
    n1=idiotie xérodermique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=60
  228. pseudo-hypoparathyroïdie --- r_associated #0: 60 --> en:classical phenylketonuria
    n1=pseudo-hypoparathyroïdie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=60
  229. pseudo-hypoparathyroïdisme --- r_associated #0: 60 --> en:classical phenylketonuria
    n1=pseudo-hypoparathyroïdisme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=60
  230. pterygium colli --- r_associated #0: 60 --> en:classical phenylketonuria
    n1=pterygium colli | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=60
  231. syndrome de de Barsy --- r_associated #0: 60 --> en:classical phenylketonuria
    n1=syndrome de de Barsy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=60
  232. syndrome de dubin-johnson --- r_associated #0: 60 --> en:classical phenylketonuria
    n1=syndrome de dubin-johnson | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=60
  233. en:De Sanctis-Cacchione syndrome --- r_associated #0: 59 --> en:classical phenylketonuria
    n1=en:De Sanctis-Cacchione syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=59
  234. en:cheilognathopalatoschisis --- r_associated #0: 59 --> en:classical phenylketonuria
    n1=en:cheilognathopalatoschisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=59
  235. en:pterygium colli --- r_associated #0: 59 --> en:classical phenylketonuria
    n1=en:pterygium colli | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=59
  236. pseudohypoparathyroïdisme --- r_associated #0: 58 --> en:classical phenylketonuria
    n1=pseudohypoparathyroïdisme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=58
  237. pseudohypoparathyroïdie --- r_associated #0: 57 --> en:classical phenylketonuria
    n1=pseudohypoparathyroïdie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=57
  238. en:mucopolysaccharidosis type i --- r_associated #0: 56 --> en:classical phenylketonuria
    n1=en:mucopolysaccharidosis type i | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=56
  239. en:transitory amino acid metabolic disorder --- r_associated #0: 56 --> en:classical phenylketonuria
    n1=en:transitory amino acid metabolic disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=56
  240. hyperlipémie --- r_associated #0: 56 --> en:classical phenylketonuria
    n1=hyperlipémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=56
  241. otocéphale --- r_associated #0: 56 --> en:classical phenylketonuria
    n1=otocéphale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=56
  242. sphingolipidose --- r_associated #0: 56 --> en:classical phenylketonuria
    n1=sphingolipidose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=56
  243. Xeroderma pigmentosum --- r_associated #0: 55 --> en:classical phenylketonuria
    n1=Xeroderma pigmentosum | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=55
  244. bec de lièvre --- r_associated #0: 55 --> en:classical phenylketonuria
    n1=bec de lièvre | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=55
  245. cheilo-gnatho-palatoschisis --- r_associated #0: 55 --> en:classical phenylketonuria
    n1=cheilo-gnatho-palatoschisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=55
  246. cheilognathopalatoschisis --- r_associated #0: 55 --> en:classical phenylketonuria
    n1=cheilognathopalatoschisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=55
  247. en:de barsy syndrome --- r_associated #0: 55 --> en:classical phenylketonuria
    n1=en:de barsy syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=55
  248. en:hyperlipidemia --- r_associated #0: 55 --> en:classical phenylketonuria
    n1=en:hyperlipidemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=55
  249. en:mucopolysaccharidosis i --- r_associated #0: 55 --> en:classical phenylketonuria
    n1=en:mucopolysaccharidosis i | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=55
  250. en:pseudohypoparathyroidism --- r_associated #0: 55 --> en:classical phenylketonuria
    n1=en:pseudohypoparathyroidism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=55
  251. en:situs mutatus --- r_associated #0: 55 --> en:classical phenylketonuria
    n1=en:situs mutatus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=55
  252. hypertrophie staturale avec macroglossie et omphalocèle --- r_associated #0: 55 --> en:classical phenylketonuria
    n1=hypertrophie staturale avec macroglossie et omphalocèle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=55
  253. syndrome de rett --- r_associated #0: 55 --> en:classical phenylketonuria
    n1=syndrome de rett | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=55
  254. trouble métabolique transitoire des acides aminés --- r_associated #0: 55 --> en:classical phenylketonuria
    n1=trouble métabolique transitoire des acides aminés | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=55
  255. syndrome de Dubin-Johnson --- r_associated #0: 54 --> en:classical phenylketonuria
    n1=syndrome de Dubin-Johnson | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=54
  256. syndrome tricho-rhino-phalangien de type II --- r_associated #0: 54 --> en:classical phenylketonuria
    n1=syndrome tricho-rhino-phalangien de type II | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=54
  257. vice de conformation --- r_associated #0: 53 --> en:classical phenylketonuria
    n1=vice de conformation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=53
  258. congenital --- r_associated #0: 52 --> en:classical phenylketonuria
    n1=congenital | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=52
  259. congénital --- r_associated #0: 52 --> en:classical phenylketonuria
    n1=congénital | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=52
  260. en:keratoconus posticus --- r_associated #0: 52 --> en:classical phenylketonuria
    n1=en:keratoconus posticus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=52
  261. fièvre --- r_associated #0: 52 --> en:classical phenylketonuria
    n1=fièvre | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=52
  262. ectopie cardiaque --- r_associated #0: 51 --> en:classical phenylketonuria
    n1=ectopie cardiaque | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=51
  263. en:down syndrome --- r_associated #0: 51 --> en:classical phenylketonuria
    n1=en:down syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=51
  264. en:tay-sachs disease --- r_associated #0: 51 --> en:classical phenylketonuria
    n1=en:tay-sachs disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=51
  265. en:Down syndrome --- r_associated #0: 50 --> en:classical phenylketonuria
    n1=en:Down syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=50
  266. en:Tay-Sachs disease --- r_associated #0: 50 --> en:classical phenylketonuria
    n1=en:Tay-Sachs disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=50
  267. en:Wolman's disease --- r_associated #0: 50 --> en:classical phenylketonuria
    n1=en:Wolman's disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=50
  268. en:glutaric aciduria, type 1 --- r_associated #0: 50 --> en:classical phenylketonuria
    n1=en:glutaric aciduria, type 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=50
  269. en:hydrencephalus --- r_associated #0: 50 --> en:classical phenylketonuria
    n1=en:hydrencephalus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=50
  270. en:macroglossia --- r_associated #0: 50 --> en:classical phenylketonuria
    n1=en:macroglossia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=50
  271. en:short stature --- r_associated #0: 50 --> en:classical phenylketonuria
    n1=en:short stature | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=50
  272. retard mental, retard de croissance, surdité, microgénitalisme lié au sexe --- r_associated #0: 50 --> en:classical phenylketonuria
    n1=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=50
  273. xérodermite pigmentaire --- r_associated #0: 50 --> en:classical phenylketonuria
    n1=xérodermite pigmentaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=50
  274. chorée de huntington --- r_associated #0: 49 --> en:classical phenylketonuria
    n1=chorée de huntington | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=49
  275. ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) --- r_associated #0: 49 --> en:classical phenylketonuria
    n1=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=49
  276. en:heterotaxy syndrome --- r_associated #0: 48 --> en:classical phenylketonuria
    n1=en:heterotaxy syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=48
  277. en:teratosis --- r_associated #0: 48 --> en:classical phenylketonuria
    n1=en:teratosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=48
  278. en:palate-blepharophimosis --- r_associated #0: 47 --> en:classical phenylketonuria
    n1=en:palate-blepharophimosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=47
  279. en:trichorhinophalangeal syndrome type II --- r_associated #0: 47 --> en:classical phenylketonuria
    n1=en:trichorhinophalangeal syndrome type II | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=47
  280. idiotie phénylpyruvique --- r_associated #0: 47 --> en:classical phenylketonuria
    n1=idiotie phénylpyruvique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=47
  281. dysplasie ectodermique --- r_associated #0: 46 --> en:classical phenylketonuria
    n1=dysplasie ectodermique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=46
  282. en:harelip --- r_associated #0: 46 --> en:classical phenylketonuria
    n1=en:harelip | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=46
  283. en:phenylpyruvic oligophrenia --- r_associated #0: 46 --> en:classical phenylketonuria
    n1=en:phenylpyruvic oligophrenia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=46
  284. en:prader-willi syndrome --- r_associated #0: 46 --> en:classical phenylketonuria
    n1=en:prader-willi syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=46
  285. phénylcétonurie --- r_associated #0: 46 --> en:classical phenylketonuria
    n1=phénylcétonurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=46
  286. puberté précoce --- r_associated #0: 46 --> en:classical phenylketonuria
    n1=puberté précoce | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=46
  287. xanthomatose cérébro-tendineuse --- r_associated #0: 46 --> en:classical phenylketonuria
    n1=xanthomatose cérébro-tendineuse | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=46
  288. xanthomatose cérébrotendineuse --- r_associated #0: 46 --> en:classical phenylketonuria
    n1=xanthomatose cérébrotendineuse | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=46
  289. en:Prader-Willi syndrome --- r_associated #0: 45 --> en:classical phenylketonuria
    n1=en:Prader-Willi syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=45
  290. en:cerebrotendinous xanthomatosis --- r_associated #0: 45 --> en:classical phenylketonuria
    n1=en:cerebrotendinous xanthomatosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=45
  291. en:ectodermal dysplasia --- r_associated #0: 45 --> en:classical phenylketonuria
    n1=en:ectodermal dysplasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=45
  292. en:exomphalos --- r_associated #0: 45 --> en:classical phenylketonuria
    n1=en:exomphalos | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=45
  293. en:mental deficiency --- r_associated #0: 45 --> en:classical phenylketonuria
    n1=en:mental deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=45
  294. en:phenylketonuria --- r_associated #0: 45 --> en:classical phenylketonuria
    n1=en:phenylketonuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=45
  295. fever --- r_associated #0: 45 --> en:classical phenylketonuria
    n1=fever | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=45
  296. globulinurie --- r_associated #0: 45 --> en:classical phenylketonuria
    n1=globulinurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=45
  297. hypertélorisme-microtie-fente faciale --- r_associated #0: 45 --> en:classical phenylketonuria
    n1=hypertélorisme-microtie-fente faciale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=45
  298. intolérance au fructose --- r_associated #0: 45 --> en:classical phenylketonuria
    n1=intolérance au fructose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=45
  299. mucolipidose type II --- r_associated #0: 45 --> en:classical phenylketonuria
    n1=mucolipidose type II | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=45
  300. mucolipidose type ii --- r_associated #0: 45 --> en:classical phenylketonuria
    n1=mucolipidose type ii | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=45
  301. Puberté précoce --- r_associated #0: 44 --> en:classical phenylketonuria
    n1=Puberté précoce | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=44
  302. en:gigantism and hyperplastic visceromegaly --- r_associated #0: 44 --> en:classical phenylketonuria
    n1=en:gigantism and hyperplastic visceromegaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=44
  303. en:major physical defect --- r_associated #0: 44 --> en:classical phenylketonuria
    n1=en:major physical defect | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=44
  304. en:physical defect --- r_associated #0: 44 --> en:classical phenylketonuria
    n1=en:physical defect | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=44
  305. en:precocious puberty --- r_associated #0: 44 --> en:classical phenylketonuria
    n1=en:precocious puberty | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=44
  306. en:situs inversus viscerum --- r_associated #0: 44 --> en:classical phenylketonuria
    n1=en:situs inversus viscerum | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=44
  307. en:williams syndrome --- r_associated #0: 44 --> en:classical phenylketonuria
    n1=en:williams syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=44
  308. maladie de wolman --- r_associated #0: 44 --> en:classical phenylketonuria
    n1=maladie de wolman | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=44
  309. polyurie --- r_associated #0: 44 --> en:classical phenylketonuria
    n1=polyurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=44
  310. sirop d'érable (urine à odeur de) --- r_associated #0: 44 --> en:classical phenylketonuria
    n1=sirop d'érable (urine à odeur de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=44
  311. télécanthus-hypertélorisme-strabisme (syndrome) --- r_associated #0: 44 --> en:classical phenylketonuria
    n1=télécanthus-hypertélorisme-strabisme (syndrome) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=44
  312. anomalie du développement --- r_associated #0: 43 --> en:classical phenylketonuria
    n1=anomalie du développement | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=43
  313. en:hereditary fructose intolerance --- r_associated #0: 43 --> en:classical phenylketonuria
    n1=en:hereditary fructose intolerance | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=43
  314. en:marfanoid mental retardation syndrome --- r_associated #0: 43 --> en:classical phenylketonuria
    n1=en:marfanoid mental retardation syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=43
  315. en:metabolic decompensation during febrile illness (patient b) --- r_associated #0: 43 --> en:classical phenylketonuria
    n1=en:metabolic decompensation during febrile illness (patient b) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=43
  316. en:trisomy 17 --- r_associated #0: 43 --> en:classical phenylketonuria
    n1=en:trisomy 17 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=43
  317. en:x-linked intellectual disability stevenson type --- r_associated #0: 43 --> en:classical phenylketonuria
    n1=en:x-linked intellectual disability stevenson type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=43
  318. maladie de Roger --- r_associated #0: 43 --> en:classical phenylketonuria
    n1=maladie de Roger | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=43
  319. en:abnormal urine odor --- r_associated #0: 42 --> en:classical phenylketonuria
    n1=en:abnormal urine odor | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=42
  320. en:globulinuria --- r_associated #0: 42 --> en:classical phenylketonuria
    n1=en:globulinuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=42
  321. en:nonketotic hypoglycemia --- r_associated #0: 42 --> en:classical phenylketonuria
    n1=en:nonketotic hypoglycemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=42
  322. en:other and unspecified congenital anomalies --- r_associated #0: 42 --> en:classical phenylketonuria
    n1=en:other and unspecified congenital anomalies | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=42
  323. en:paroxysmal nocturnal hemoglobinuria --- r_associated #0: 42 --> en:classical phenylketonuria
    n1=en:paroxysmal nocturnal hemoglobinuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=42
  324. goutte --- r_associated #0: 42 --> en:classical phenylketonuria
    n1=goutte | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=42
  325. hypertélorisme, hypospadias, polysyndactylie (syndrome) --- r_associated #0: 42 --> en:classical phenylketonuria
    n1=hypertélorisme, hypospadias, polysyndactylie (syndrome) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=42
  326. hérédité autosomale récessive --- r_associated #0: 42 --> en:classical phenylketonuria
    n1=hérédité autosomale récessive | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=42
  327. phacomatose congenitale --- r_associated #0: 42 --> en:classical phenylketonuria
    n1=phacomatose congenitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=42
  328. tubulopathie rénale, diabète sucré, ataxie cérébelleuse secondaire à une duplication de l'ADN mitochondrial --- r_associated #0: 42 --> en:classical phenylketonuria
    n1=tubulopathie rénale, diabète sucré, ataxie cérébelleuse secondaire à une duplication de l'ADN mitochondrial | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=42
  329. Fenn (diagramme de) --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=Fenn (diagramme de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  330. chorée de sydenham --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=chorée de sydenham | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  331. déficit en semialdéhyde succinique-déshydrogénase --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=déficit en semialdéhyde succinique-déshydrogénase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  332. en:Williams syndrome --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=en:Williams syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  333. en:bacteriuria in pregnancy --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=en:bacteriuria in pregnancy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  334. en:congenital flexion deformity --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=en:congenital flexion deformity | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  335. en:mental retardation spasticity ectrodactyly --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=en:mental retardation spasticity ectrodactyly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  336. en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  337. en:polyuria --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=en:polyuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  338. en:thoracogastroschisis --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=en:thoracogastroschisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  339. en:upper limb defect with eye and ear abnormalities syndrome --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=en:upper limb defect with eye and ear abnormalities syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  340. en:waardenburg anophthalmia syndrome --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=en:waardenburg anophthalmia syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  341. hétérotaxie --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=hétérotaxie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  342. imperforation anale --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=imperforation anale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  343. pyurie --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=pyurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  344. rétention des chylomicrons (maladie de la) --- r_associated #0: 41 --> en:classical phenylketonuria
    n1=rétention des chylomicrons (maladie de la) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=41
  345. Walker-Warburg (syndrome de) --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=Walker-Warburg (syndrome de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  346. diabète sucré de type 2 avec surdité --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=diabète sucré de type 2 avec surdité | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  347. en:adrenal cytomegaly --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=en:adrenal cytomegaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  348. en:hereditary adrenal unresponsiveness to corticotropin --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=en:hereditary adrenal unresponsiveness to corticotropin | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  349. en:heterotaxy --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=en:heterotaxy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  350. en:hnsha due to aldolase a deficiency --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=en:hnsha due to aldolase a deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  351. en:laparoschisis --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=en:laparoschisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  352. en:lujan fryns syndrome --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=en:lujan fryns syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  353. en:pancreatic alpha-amylase deficiency --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=en:pancreatic alpha-amylase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  354. en:pneumatouria --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=en:pneumatouria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  355. en:pyuria --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=en:pyuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  356. en:ventricular septal defect --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=en:ventricular septal defect | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  357. en:xanthinuria, type i --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=en:xanthinuria, type i | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  358. macroglossie --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=macroglossie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  359. maladie de Tay-sachs --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=maladie de Tay-sachs | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  360. maladie de cœur --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=maladie de cœur | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  361. maladie de coeur --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=maladie de coeur | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  362. maladie de tay-sachs --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=maladie de tay-sachs | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  363. nanisme, retard mental, anomalies oculaires --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=nanisme, retard mental, anomalies oculaires | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  364. van Bogaert (xanthomatose cérébrotendineuse de) --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=van Bogaert (xanthomatose cérébrotendineuse de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  365. xanthomatose cérébrotendineuse de Van Bogaert --- r_associated #0: 40 --> en:classical phenylketonuria
    n1=xanthomatose cérébrotendineuse de Van Bogaert | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=40
  366. Maladie de Huntington --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=Maladie de Huntington | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  367. en:antley-bixler syndrome, autosomal dominant --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=en:antley-bixler syndrome, autosomal dominant | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  368. en:autosomal recessive inheritance --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=en:autosomal recessive inheritance | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  369. en:autosomal recessive ocular albinism --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=en:autosomal recessive ocular albinism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  370. en:carbamoyl-phosphate synthetase i deficiency --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=en:carbamoyl-phosphate synthetase i deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  371. en:chylomicron retention disease --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=en:chylomicron retention disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  372. en:developmental immaturity --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=en:developmental immaturity | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  373. en:disorder of histidine metabolism --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=en:disorder of histidine metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  374. en:gaze palsy, familial horizontal, with progressive scoliosis --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=en:gaze palsy, familial horizontal, with progressive scoliosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  375. en:heart defects limb shortening --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=en:heart defects limb shortening | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  376. en:langer-giedion syndrome --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=en:langer-giedion syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  377. en:microalbuminuria --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=en:microalbuminuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  378. en:multicentric osteolysis nodulosis arthropathy spectrum --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=en:multicentric osteolysis nodulosis arthropathy spectrum | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  379. faciès anormal, retard de croissance et retard mental --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=faciès anormal, retard de croissance et retard mental | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  380. goniodysgénésie-retard mental-petite taille (syndrome) --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=goniodysgénésie-retard mental-petite taille (syndrome) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  381. imperforation de l'anus --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=imperforation de l'anus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  382. oligophrénie phénylpyruvique --- r_associated #0: 39 --> en:classical phenylketonuria
    n1=oligophrénie phénylpyruvique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  383. dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental --- r_associated #0: 38 --> en:classical phenylketonuria
    n1=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=38
  384. en:bestrophinopathy, autosomal recessive --- r_associated #0: 38 --> en:classical phenylketonuria
    n1=en:bestrophinopathy, autosomal recessive | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=38
  385. en:imperforate anus --- r_associated #0: 38 --> en:classical phenylketonuria
    n1=en:imperforate anus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=38
  386. en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome --- r_associated #0: 38 --> en:classical phenylketonuria
    n1=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=38
  387. en:mildly elevated glucose --- r_associated #0: 38 --> en:classical phenylketonuria
    n1=en:mildly elevated glucose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=38
  388. en:richards-rundle syndrome --- r_associated #0: 38 --> en:classical phenylketonuria
    n1=en:richards-rundle syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=38
  389. en:storage disease --- r_associated #0: 38 --> en:classical phenylketonuria
    n1=en:storage disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=38
  390. hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle --- r_associated #0: 38 --> en:classical phenylketonuria
    n1=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=38
  391. diabète, photomyoclonies, surdité, néphropathie et dysfonction cérébrale --- r_associated #0: 37 --> en:classical phenylketonuria
    n1=diabète, photomyoclonies, surdité, néphropathie et dysfonction cérébrale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=37
  392. en:3-methylglutaconic aciduria type 5 --- r_associated #0: 37 --> en:classical phenylketonuria
    n1=en:3-methylglutaconic aciduria type 5 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=37
  393. en:bothnia retinal dystrophy --- r_associated #0: 37 --> en:classical phenylketonuria
    n1=en:bothnia retinal dystrophy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=37
  394. en:cask related intellectual disability --- r_associated #0: 37 --> en:classical phenylketonuria
    n1=en:cask related intellectual disability | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=37
  395. en:congenital abnormal fusion --- r_associated #0: 37 --> en:classical phenylketonuria
    n1=en:congenital abnormal fusion | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=37
  396. en:congenital anomaly of back --- r_associated #0: 37 --> en:classical phenylketonuria
    n1=en:congenital anomaly of back | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=37
  397. en:congenital deformity of pharynx --- r_associated #0: 37 --> en:classical phenylketonuria
    n1=en:congenital deformity of pharynx | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=37
  398. en:congenital extension deformity --- r_associated #0: 37 --> en:classical phenylketonuria
    n1=en:congenital extension deformity | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=37
  399. en:exenkephaly --- r_associated #0: 37 --> en:classical phenylketonuria
    n1=en:exenkephaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=37
  400. en:pseudocholinesterase deficiency --- r_associated #0: 37 --> en:classical phenylketonuria
    n1=en:pseudocholinesterase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=37
  401. en:purine-pyrimidine metabolism, inborn errors --- r_associated #0: 37 --> en:classical phenylketonuria
    n1=en:purine-pyrimidine metabolism, inborn errors | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=37
  402. en:succinic semialdehyde dehydrogenase deficiency --- r_associated #0: 37 --> en:classical phenylketonuria
    n1=en:succinic semialdehyde dehydrogenase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=37
  403. nystagmus congénital isolé --- r_associated #0: 37 --> en:classical phenylketonuria
    n1=nystagmus congénital isolé | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=37
  404. protoproporphyrie érythropoïétique --- r_associated #0: 37 --> en:classical phenylketonuria
    n1=protoproporphyrie érythropoïétique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=37
  405. Trouble anxieux --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=Trouble anxieux | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  406. déficit en prolidase --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=déficit en prolidase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  407. en:brain calcification rajab type --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:brain calcification rajab type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  408. en:childhood hypophosphatasia (disorder) --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  409. en:cleft palate --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:cleft palate | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  410. en:congenital flat back deformity --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:congenital flat back deformity | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  411. en:disorder of creatine synthesis --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:disorder of creatine synthesis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  412. en:dyslipidemia (in some patients) --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:dyslipidemia (in some patients) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  413. en:erythropoietic protoporphyria --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:erythropoietic protoporphyria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  414. en:goniodysgenesis-mental retardation-short stature syndrome --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  415. en:hyperlipemia --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:hyperlipemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  416. en:maple-tree syrup disease --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:maple-tree syrup disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  417. en:microcephaly deafness syndrome --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:microcephaly deafness syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  418. en:muscle d-lactate dehydrogenase deficiency --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:muscle d-lactate dehydrogenase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  419. en:neural tube defect --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:neural tube defect | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  420. en:ombilical hernia --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:ombilical hernia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  421. en:posterior urethral valve --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:posterior urethral valve | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  422. en:renal tubulopathy --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=en:renal tubulopathy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  423. fissure faciale --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=fissure faciale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  424. hyperphosphaturie --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=hyperphosphaturie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  425. maladie de Gaucher --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=maladie de Gaucher | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  426. maladie de Marchiafava-Micheli --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=maladie de Marchiafava-Micheli | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  427. maladie de Niemann-Pick --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=maladie de Niemann-Pick | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  428. phénylcétonurie de type 1 --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=phénylcétonurie de type 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  429. sirénomélie --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=sirénomélie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  430. syndrome de Lowe --- r_associated #0: 36 --> en:classical phenylketonuria
    n1=syndrome de Lowe | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  431. Maladie congénitale --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=Maladie congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  432. Wolman (maladie de) --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=Wolman (maladie de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  433. diabète (accidents vasculaires cérébraux du) --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=diabète (accidents vasculaires cérébraux du) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  434. déficit en phénylalanine hydroxylase --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=déficit en phénylalanine hydroxylase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  435. en:1p21.3 microdeletion syndrome --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:1p21.3 microdeletion syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  436. en:21-hydroxylase deficiency --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:21-hydroxylase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  437. en:3-methylglutaconic aciduria type 1 --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:3-methylglutaconic aciduria type 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  438. en:Niemann-Pick disease --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:Niemann-Pick disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  439. en:adult fanconi syndrome --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:adult fanconi syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  440. en:adult hypophosphatasia (disorder) --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:adult hypophosphatasia (disorder) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  441. en:amelogenesis imperfecta - recessive - rough --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:amelogenesis imperfecta - recessive - rough | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  442. en:amino acid transport disorders, inborn --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:amino acid transport disorders, inborn | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  443. en:arginine:glycine amidinotransferase deficiency --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:arginine:glycine amidinotransferase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  444. en:autosomal recessive scid --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:autosomal recessive scid | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  445. en:autosomal recessive spastic paraplegia type 39 --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:autosomal recessive spastic paraplegia type 39 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  446. en:behrens baumann dust syndrome --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:behrens baumann dust syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  447. en:cardiac and circulatory congenital anomalies --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:cardiac and circulatory congenital anomalies | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  448. en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  449. en:common atrioventricular orifice in double inlet ventricle --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:common atrioventricular orifice in double inlet ventricle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  450. en:congenital abnormality of lower limb and/or pelvic girdle --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:congenital abnormality of lower limb and/or pelvic girdle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  451. en:congenital amegakaryocytic thrombocytopenia --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:congenital amegakaryocytic thrombocytopenia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  452. en:congenital analbuminemia --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:congenital analbuminemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  453. en:congenital anomaly of trunk --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:congenital anomaly of trunk | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  454. en:congenital deformity of clavicle --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:congenital deformity of clavicle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  455. en:congenital deformity of labyrinth --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:congenital deformity of labyrinth | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  456. en:congenital disorder of glycosylation type 2e --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:congenital disorder of glycosylation type 2e | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  457. en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  458. en:congenital plasminogen activator inhibitor deficiency type 1 --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:congenital plasminogen activator inhibitor deficiency type 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  459. en:congenital sequestration --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:congenital sequestration | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  460. en:cystinuria --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:cystinuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  461. en:defect in post-translational modification of lysosomal enzymes --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:defect in post-translational modification of lysosomal enzymes | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  462. en:deficiency of glucosyltransferase 1 --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:deficiency of glucosyltransferase 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  463. en:disorder of sialic acid metabolism --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:disorder of sialic acid metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  464. en:donnai-barrow syndrome --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:donnai-barrow syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  465. en:ectromelia --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:ectromelia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  466. en:encephalopathy due to sulfite oxidase deficiency --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:encephalopathy due to sulfite oxidase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  467. en:enterokinase deficiency --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:enterokinase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  468. en:epidermolysis bullosa simplex with pyloric atresia --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:epidermolysis bullosa simplex with pyloric atresia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  469. en:ethanolaminosis --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:ethanolaminosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  470. en:factor v and factor viii, combined deficiency of --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:factor v and factor viii, combined deficiency of | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  471. en:fatty acid hydroxylase-associated neurodegeneration --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:fatty acid hydroxylase-associated neurodegeneration | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  472. en:generalized peeling skin syndrome --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:generalized peeling skin syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  473. en:hall riggs syndrome --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:hall riggs syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  474. en:hnsha due to diphosphoglycerate mutase deficiency --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  475. en:homocarnosinosis --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:homocarnosinosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  476. en:hyperhomocysteinemia --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:hyperhomocysteinemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  477. en:hypermagnesuria --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:hypermagnesuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  478. en:hyperphenylalaninemia, non phenylketonuric --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:hyperphenylalaninemia, non phenylketonuric | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  479. en:hypoketotic hypoglycemia --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:hypoketotic hypoglycemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  480. en:hypomandibular faciocranial dysostosis --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:hypomandibular faciocranial dysostosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  481. en:inborn error of glutathione metabolism --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:inborn error of glutathione metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  482. en:intestinal malrotation --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:intestinal malrotation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  483. en:kuskokwim disease --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:kuskokwim disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  484. en:lissencephaly syndrome, norman-roberts type --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:lissencephaly syndrome, norman-roberts type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  485. en:microcephaly cervical spine fusion anomalies --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:microcephaly cervical spine fusion anomalies | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  486. en:microcephaly-capillary malformation syndrome --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  487. en:neonatal progeroid syndrome --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:neonatal progeroid syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  488. en:neuraminidase deficiency --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:neuraminidase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  489. en:nutritional and metabolic diseases --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:nutritional and metabolic diseases | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  490. en:nutritional mental retardation --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:nutritional mental retardation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  491. en:odontohypophosphatasia (disorder) --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:odontohypophosphatasia (disorder) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  492. en:oroticaciduria congenital --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:oroticaciduria congenital | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  493. en:other congenital anomalies of limbs --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:other congenital anomalies of limbs | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  494. en:other mental retardation --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:other mental retardation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  495. en:phenylketonuria diet education --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:phenylketonuria diet education | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  496. en:ppp2r5d-related intellectual disability --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:ppp2r5d-related intellectual disability | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  497. en:prader-willi habitus, osteopenia, and camptodactyly --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:prader-willi habitus, osteopenia, and camptodactyly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  498. en:propionic acidemia --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:propionic acidemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  499. en:pseudotrisomy 13 syndrome --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:pseudotrisomy 13 syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  500. en:reduced phenylalanine hydroxylase activity --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:reduced phenylalanine hydroxylase activity | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  501. en:retinitis punctata albescens (disorder) --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:retinitis punctata albescens (disorder) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  502. en:severe mental retardation (i.q. 20-34) --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:severe mental retardation (i.q. 20-34) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  503. en:split-hand/foot malformation 3 --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:split-hand/foot malformation 3 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  504. en:spondylocarpotarsal synostosis syndrome --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:spondylocarpotarsal synostosis syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  505. en:spondyloepiphyseal dysplasia, omani type --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:spondyloepiphyseal dysplasia, omani type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  506. en:uv-sensitive syndrome --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:uv-sensitive syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  507. en:x-linked intellectual disability seemanova type --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=en:x-linked intellectual disability seemanova type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  508. fissure palatine --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=fissure palatine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  509. syndrome de synostose spondylo-carpo-tarsale --- r_associated #0: 35 --> en:classical phenylketonuria
    n1=syndrome de synostose spondylo-carpo-tarsale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  510. eczema --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=eczema | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  511. eczéma --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=eczéma | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  512. en:3-methylglutaconic aciduria type iv --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:3-methylglutaconic aciduria type iv | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  513. en:adducted thumbs and arthrogryposis syndrome christian type --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:adducted thumbs and arthrogryposis syndrome christian type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  514. en:al awadi syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:al awadi syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  515. en:amino acid transport disorder --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:amino acid transport disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  516. en:arakawa syndrome ii --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:arakawa syndrome ii | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  517. en:argininemia --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:argininemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  518. en:biotinidase deficiency --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:biotinidase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  519. en:borderline mental retardation (i.q. 70-85) --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:borderline mental retardation (i.q. 70-85) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  520. en:borjeson-forssman-lehmann syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:borjeson-forssman-lehmann syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  521. en:brachioskeletogenital syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:brachioskeletogenital syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  522. en:butyryl-coa dehydrogenase deficiency --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:butyryl-coa dehydrogenase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  523. en:caudal dysplasia --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:caudal dysplasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  524. en:chondrodysplasia punctata syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:chondrodysplasia punctata syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  525. en:chromaturia --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:chromaturia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  526. en:congenital anomaly of skeletal bone --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:congenital anomaly of skeletal bone | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  527. en:congenital anomaly of visual system --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:congenital anomaly of visual system | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  528. en:congenital bowing of long bone --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:congenital bowing of long bone | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  529. en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  530. en:congenital disorder of glycosylation type 1h --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:congenital disorder of glycosylation type 1h | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  531. en:congenital disorder of glycosylation type ig --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:congenital disorder of glycosylation type ig | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  532. en:congenital enlargement --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:congenital enlargement | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  533. en:congenital malposition --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:congenital malposition | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  534. en:cutis laxa, autosomal recessive --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:cutis laxa, autosomal recessive | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  535. en:decreased hdl cholesterol --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:decreased hdl cholesterol | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  536. en:deficiency of steryl-sulfatase --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:deficiency of steryl-sulfatase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  537. en:diaphanospondylodysostosis --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:diaphanospondylodysostosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  538. en:digeorge syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:digeorge syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  539. en:dihydropyrimidinase deficiency --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:dihydropyrimidinase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  540. en:disorder of glycosaminoglycan metabolism --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:disorder of glycosaminoglycan metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  541. en:ectodermal dysplasia/ skin fragility syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:ectodermal dysplasia/ skin fragility syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  542. en:eczema --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:eczema | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  543. en:facial cleft --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:facial cleft | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  544. en:familial c3b inhibitor deficiency syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:familial c3b inhibitor deficiency syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  545. en:familial erythrocytosis due to diphosphoglycerate mutase deficiency --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  546. en:glucose-6-phosphate dehydrogenase deficiency --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:glucose-6-phosphate dehydrogenase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  547. en:glutathione synthetase deficiency --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:glutathione synthetase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  548. en:haematinuria --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:haematinuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  549. en:hematuria --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:hematuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  550. en:hereditary factor x deficiency disease --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:hereditary factor x deficiency disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  551. en:hereditary orotic aciduria --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:hereditary orotic aciduria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  552. en:histidinemia --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:histidinemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  553. en:hnsha due to hexokinase deficiency --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:hnsha due to hexokinase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  554. en:hnsha due to nadh diaphorase deficiency --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:hnsha due to nadh diaphorase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  555. en:hydroxykynureninuria --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:hydroxykynureninuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  556. en:hyperglycinemia --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:hyperglycinemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  557. en:hypertrophy of clitoris --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:hypertrophy of clitoris | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  558. en:inborn errors of bilirubin metabolism --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:inborn errors of bilirubin metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  559. en:increased urinary o-hydroxyphenylacetic acid, phenylpyruvic acid, phenylacetic acid and phenylacetylglutamine --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:increased urinary o-hydroxyphenylacetic acid, phenylpyruvic acid, phenylacetic acid and phenylacetylglutamine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  560. en:isolated hyperchlorhidrosis --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:isolated hyperchlorhidrosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  561. en:isovaleric acidemia --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:isovaleric acidemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  562. en:ketoses, metabolic --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:ketoses, metabolic | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  563. en:lactose intolerance, adult type --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:lactose intolerance, adult type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  564. en:laryngeal atresia --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:laryngeal atresia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  565. en:late-onset junctional epidermolysis bullosa --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:late-onset junctional epidermolysis bullosa | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  566. en:laurence-moon syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:laurence-moon syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  567. en:maroteaux-lamy syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:maroteaux-lamy syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  568. en:masa syndrome (disorder) --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:masa syndrome (disorder) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  569. en:maternal hyperphenylalaninemia teratogenic --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:maternal hyperphenylalaninemia teratogenic | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  570. en:mcdonough syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:mcdonough syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  571. en:mental dullness --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:mental dullness | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  572. en:methylcrotonyl-coa carboxylase deficiency --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:methylcrotonyl-coa carboxylase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  573. en:methylene thf reductase deficiency and homocystinuria --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:methylene thf reductase deficiency and homocystinuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  574. en:methylenetetrahydrofolate reductase gene mutation --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:methylenetetrahydrofolate reductase gene mutation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  575. en:monster (disorder) --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:monster (disorder) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  576. en:morm syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:morm syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  577. en:multiple carboxylase deficiency --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:multiple carboxylase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  578. en:nitrituria --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:nitrituria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  579. en:oculocerebrorenal syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:oculocerebrorenal syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  580. en:oculocutaneous albinism type 4 --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:oculocutaneous albinism type 4 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  581. en:odontogenic cyst --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:odontogenic cyst | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  582. en:other congenital anomalies of nervous system --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:other congenital anomalies of nervous system | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  583. en:other specified mental retardation --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:other specified mental retardation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  584. en:persistent cloaca --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:persistent cloaca | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  585. en:placental steroid sulfatase deficiency --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:placental steroid sulfatase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  586. en:profound intellectual disabilities --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:profound intellectual disabilities | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  587. en:prolidase deficiency --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:prolidase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  588. en:prolonged electroretinal response suppression --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:prolonged electroretinal response suppression | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  589. en:reduced energy expenditure --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:reduced energy expenditure | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  590. en:renpenning syndrome 1 --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:renpenning syndrome 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  591. en:schinzel-giedion midface-retraction syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:schinzel-giedion midface-retraction syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  592. en:semenuria --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:semenuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  593. en:sirenomelia --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:sirenomelia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  594. en:sjogren-larsson syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:sjogren-larsson syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  595. en:spastic ataxia, charlevoix-saguenay type --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:spastic ataxia, charlevoix-saguenay type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  596. en:spinal muscular atrophy with respiratory distress 1 --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:spinal muscular atrophy with respiratory distress 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  597. en:spondylo-ocular syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:spondylo-ocular syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  598. en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  599. en:syndrome of apparent mineralocorticoid excess --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:syndrome of apparent mineralocorticoid excess | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  600. en:trisomy xq28 syndrome --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:trisomy xq28 syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  601. en:unclassified metabolic disorder --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:unclassified metabolic disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  602. en:werdnig-hoffmann disease --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:werdnig-hoffmann disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  603. en:x-linked intellectual disability armfield type --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:x-linked intellectual disability armfield type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  604. en:zellweger-like syndrome without peroxisomal anomaly --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=en:zellweger-like syndrome without peroxisomal anomaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  605. hyponatriurie --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=hyponatriurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  606. hémochromatose néonatale --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=hémochromatose néonatale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  607. imbécilité phénylpyruvique --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=imbécilité phénylpyruvique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  608. lipofuscinose neuronale céroïde infantile finlandaise --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=lipofuscinose neuronale céroïde infantile finlandaise | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  609. non précisé, bec-de-lièvre --- r_associated #0: 34 --> en:classical phenylketonuria
    n1=non précisé, bec-de-lièvre | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
  610. dysplasie ectodermique, ectrodactylie et dystrophie maculaire --- r_associated #0: 33 --> en:classical phenylketonuria
    n1=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=33
  611. en:isosthenuria --- r_associated #0: 33 --> en:classical phenylketonuria
    n1=en:isosthenuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=33
  612. en:neonatal hemochromatosis --- r_associated #0: 33 --> en:classical phenylketonuria
    n1=en:neonatal hemochromatosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=33
  613. en:neuronal ceroid lipofuscinosis --- r_associated #0: 33 --> en:classical phenylketonuria
    n1=en:neuronal ceroid lipofuscinosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=33
  614. maladie lysosomique de surcharge --- r_associated #0: 33 --> en:classical phenylketonuria
    n1=maladie lysosomique de surcharge | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=33
  615. syndrome de Laurence-Moon --- r_associated #0: 33 --> en:classical phenylketonuria
    n1=syndrome de Laurence-Moon | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=33
  616. Bec de lièvre --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=Bec de lièvre | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  617. albinisme --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=albinisme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  618. déficience intellectuelle --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=déficience intellectuelle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  619. en:12q14 microdeletion syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:12q14 microdeletion syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  620. en:acquired aminoaciduria --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:acquired aminoaciduria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  621. en:adenine phosphoribosyltransferase deficiency --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:adenine phosphoribosyltransferase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  622. en:albinism --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:albinism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  623. en:aplasia, nos --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:aplasia, nos | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  624. en:argininosuccinic aciduria --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:argininosuccinic aciduria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  625. en:benign neonatal hyperaminoaciduria --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:benign neonatal hyperaminoaciduria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  626. en:bietti crystalline corneoretinal dystrophy --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:bietti crystalline corneoretinal dystrophy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  627. en:caroli disease --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:caroli disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  628. en:cervical hypertrichosis and peripheral neuropathy syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:cervical hypertrichosis and peripheral neuropathy syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  629. en:clubfoot --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:clubfoot | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  630. en:combined malonic and methylmalonic aciduria --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:combined malonic and methylmalonic aciduria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  631. en:congenital hyperflexion of limb --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:congenital hyperflexion of limb | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  632. en:congenital hypoplasia of genital tubercle --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:congenital hypoplasia of genital tubercle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  633. en:congenital malformation syndrome related to known exogenous cause --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:congenital malformation syndrome related to known exogenous cause | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  634. en:congenital nervous system disorder --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:congenital nervous system disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  635. en:congenital urinary system abnormality --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:congenital urinary system abnormality | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  636. en:congenital vena cava abnormality --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:congenital vena cava abnormality | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  637. en:cooper jabs syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:cooper jabs syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  638. en:deafness, sensorineural, and male infertility --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:deafness, sensorineural, and male infertility | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  639. en:dehydration --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:dehydration | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  640. en:disorder of branched-chain amino acid metabolism --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:disorder of branched-chain amino acid metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  641. en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:ectodermal dysplasia with blindness syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  642. en:erythrocyte enolase deficiency --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:erythrocyte enolase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  643. en:ethmocephaly --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:ethmocephaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  644. en:fatty acid metabolism disorder --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:fatty acid metabolism disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  645. en:fetal postural deformity --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:fetal postural deformity | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  646. en:frohlich syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:frohlich syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  647. en:glycine dehydrogenase (decarboxylating) deficiency --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:glycine dehydrogenase (decarboxylating) deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  648. en:glycine encephalopathy --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:glycine encephalopathy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  649. en:hereditary elliptocytosis --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:hereditary elliptocytosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  650. en:hypermethioniuria --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:hypermethioniuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  651. en:hyperphosphaturia --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:hyperphosphaturia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  652. en:hypokalemia, familial --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:hypokalemia, familial | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  653. en:hyponatriuria --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:hyponatriuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  654. en:infantile globoid cell leukodystrophy --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:infantile globoid cell leukodystrophy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  655. en:inherited disorder of thyroid metabolism --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:inherited disorder of thyroid metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  656. en:interleukin-1 receptor-associated kinase 4 deficiency --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:interleukin-1 receptor-associated kinase 4 deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  657. en:karandikar maria kamble syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:karandikar maria kamble syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  658. en:kbg syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:kbg syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  659. en:lesch-nyhan syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:lesch-nyhan syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  660. en:lethal congenital contracture syndrome 1 --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:lethal congenital contracture syndrome 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  661. en:lethal larsen-like syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:lethal larsen-like syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  662. en:leucinosis --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:leucinosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  663. en:limb deformities, congenital --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:limb deformities, congenital | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  664. en:lipid metabolism disorder --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:lipid metabolism disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  665. en:loin pain-hematuria syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:loin pain-hematuria syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  666. en:lubs x-linked mental retardation syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:lubs x-linked mental retardation syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  667. en:lysosomal storage disease --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:lysosomal storage disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  668. en:methylmalonyl-coenzyme a mutase deficiency --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:methylmalonyl-coenzyme a mutase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  669. en:microcephaly albinism digital anomalies syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:microcephaly albinism digital anomalies syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  670. en:neonatal hypoglycemia --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:neonatal hypoglycemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  671. en:neurodegeneration with brain iron accumulation 4 --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:neurodegeneration with brain iron accumulation 4 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  672. en:neutral lipid storage disease with myopathy --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:neutral lipid storage disease with myopathy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  673. en:nonaka myopathy --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:nonaka myopathy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  674. en:oculocutaneous albinism type 6 --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:oculocutaneous albinism type 6 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  675. en:other hyperphenylalaninaemias --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:other hyperphenylalaninaemias | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  676. en:other specified congenital malformations --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:other specified congenital malformations | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  677. en:otoonychoperoneal syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:otoonychoperoneal syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  678. en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  679. en:pili torti onychodysplasia syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:pili torti onychodysplasia syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  680. en:pontocerebellar hypoplasia type 2 --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:pontocerebellar hypoplasia type 2 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  681. en:post procedural haematuria --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:post procedural haematuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  682. en:radiation-induced disorder --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:radiation-induced disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  683. en:sarcosinemia --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:sarcosinemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  684. en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  685. en:smith-magenis syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:smith-magenis syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  686. en:spondyloepiphyseal dysplasia tarda kohn type --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:spondyloepiphyseal dysplasia tarda kohn type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  687. en:steroid metabolism, inborn errors --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:steroid metabolism, inborn errors | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  688. en:telecanthus --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:telecanthus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  689. en:transient hyperphenylalaninemia --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:transient hyperphenylalaninemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  690. en:type ii acrocephalopolysyndactyly --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:type ii acrocephalopolysyndactyly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  691. en:tyrosinemia type ii --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:tyrosinemia type ii | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  692. en:tyrosinemia, type iii --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:tyrosinemia, type iii | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  693. en:urea cycle metabolism disorder --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:urea cycle metabolism disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  694. en:urocanase deficiency --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:urocanase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  695. en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  696. en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  697. en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  698. hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  699. histiocytose sinusale hémophagocytaire --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=histiocytose sinusale hémophagocytaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  700. hématurie macroscopique --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=hématurie macroscopique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  701. lipofuscinose neuronale céroïde --- r_associated #0: 32 --> en:classical phenylketonuria
    n1=lipofuscinose neuronale céroïde | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  702. atrésie --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=atrésie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  703. déficit en neuraminidase --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=déficit en neuraminidase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  704. ectromélie --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=ectromélie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  705. elliptocytose héréditaire --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=elliptocytose héréditaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  706. en:5 alpha steroid reductase 2 deficiency --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:5 alpha steroid reductase 2 deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  707. en:abnormalities, drug-induced --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:abnormalities, drug-induced | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  708. en:agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  709. en:allgrove syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:allgrove syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  710. en:amelogenesis imperfecta and gingival hyperplasia syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:amelogenesis imperfecta and gingival hyperplasia syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  711. en:aminoacylase 1 deficiency --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:aminoacylase 1 deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  712. en:arterial tortuosity syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:arterial tortuosity syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  713. en:atresia --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:atresia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  714. en:autosomal recessive distal osteolysis syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:autosomal recessive distal osteolysis syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  715. en:bamforth syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:bamforth syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  716. en:brody myopathy --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:brody myopathy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  717. en:cerebellar ataxia, cayman type --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:cerebellar ataxia, cayman type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  718. en:cheilognathoschisis --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:cheilognathoschisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  719. en:congenital anomaly of body wall --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:congenital anomaly of body wall | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  720. en:congenital cataracts, facial dysmorphism, and neuropathy --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:congenital cataracts, facial dysmorphism, and neuropathy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  721. en:congenital deformity of scapula --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:congenital deformity of scapula | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  722. en:congenital disorder of glycosylation type ia --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:congenital disorder of glycosylation type ia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  723. en:congenital hallux valgus --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:congenital hallux valgus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  724. en:congenital musculoskeletal defect --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:congenital musculoskeletal defect | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  725. en:congenital opacity --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:congenital opacity | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  726. en:congenital systemic disorder --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:congenital systemic disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  727. en:crisponi syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:crisponi syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  728. en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  729. en:deafness, progressive, with stapes fixation --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:deafness, progressive, with stapes fixation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  730. en:decreased tetrasialotransferrin --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:decreased tetrasialotransferrin | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  731. en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  732. en:disorder of aromatic amino acid metabolism --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:disorder of aromatic amino acid metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  733. en:dyskeratosis congenita, autosomal recessive --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:dyskeratosis congenita, autosomal recessive | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  734. en:episodic ketoacidosis --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:episodic ketoacidosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  735. en:familial acantholysis --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:familial acantholysis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  736. en:fatal infantile lactic acidosis with methylmalonic aciduria --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:fatal infantile lactic acidosis with methylmalonic aciduria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  737. en:fountain syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:fountain syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  738. en:fraxe intellectual disability syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:fraxe intellectual disability syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  739. en:fucosidosis --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:fucosidosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  740. en:gamma-glutamyltransferase deficiency --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:gamma-glutamyltransferase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  741. en:glycogen storage disease --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:glycogen storage disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  742. en:gracile syndrome (disorder) --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:gracile syndrome (disorder) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  743. en:hartnup disease --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:hartnup disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  744. en:hereditary factor xi deficiency disease --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:hereditary factor xi deficiency disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  745. en:hexose-6-phosphate dehydrogenase deficiency --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:hexose-6-phosphate dehydrogenase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  746. en:hnsha due to glutathione synthetase deficiency --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:hnsha due to glutathione synthetase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  747. en:hypercalciuria --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:hypercalciuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  748. en:hyperlysinemia --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:hyperlysinemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  749. en:hyperprolinemia type 2 --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:hyperprolinemia type 2 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  750. en:hypoglycemia, oral protein-induced --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:hypoglycemia, oral protein-induced | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  751. en:hypophosphatasia infantile --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:hypophosphatasia infantile | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  752. en:hypospadias-mental retardation syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:hypospadias-mental retardation syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  753. en:knobloch syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:knobloch syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  754. en:known or suspected fetal abnormality affecting management of mother --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:known or suspected fetal abnormality affecting management of mother | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  755. en:lethal congenital contracture syndrome type 3 --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:lethal congenital contracture syndrome type 3 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  756. en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  757. en:mental retardation, x-linked --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:mental retardation, x-linked | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  758. en:mental retardation, x-linked, snyder-robinson type --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:mental retardation, x-linked, snyder-robinson type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  759. en:moyamoya disease with early onset achalasia --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:moyamoya disease with early onset achalasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  760. en:myopathy with exercise intolerance, swedish type --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:myopathy with exercise intolerance, swedish type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  761. en:other specified disorders of amino-acid metabolism --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:other specified disorders of amino-acid metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  762. en:pancreatic triacylglycerol lipase deficiency --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:pancreatic triacylglycerol lipase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  763. en:partington x-linked mental retardation syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:partington x-linked mental retardation syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  764. en:perniola krajewska carnevale syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:perniola krajewska carnevale syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  765. en:phenylketonuria, maternal --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:phenylketonuria, maternal | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  766. en:pyruvate kinase deficiency --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:pyruvate kinase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  767. en:rhinocephaly --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:rhinocephaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  768. en:sinus histiocytosis with massive lymphadenopathy --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:sinus histiocytosis with massive lymphadenopathy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  769. en:smith-mccort dysplasia --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:smith-mccort dysplasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  770. en:supernumerary structure --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:supernumerary structure | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  771. en:thoracoschisis --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:thoracoschisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  772. en:transposition of great vessels --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:transposition of great vessels | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  773. en:unspecified intellectual disabilities --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:unspecified intellectual disabilities | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  774. en:unspecified mental retardation; other impairments of behaviour --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:unspecified mental retardation; other impairments of behaviour | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  775. en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  776. en:urinary abnormalities --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:urinary abnormalities | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  777. en:urine casts --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:urine casts | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  778. en:warsaw breakage syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:warsaw breakage syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  779. en:x-linked intellectual disability with acromegaly and hyperactivity syndrome --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  780. fucosidose --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=fucosidose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  781. histidinémie --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=histidinémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  782. homocarnosinose --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=homocarnosinose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  783. hypercalciurie --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=hypercalciurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  784. hyperphénylalaninémie --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=hyperphénylalaninémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  785. hyperprolinémie de type I --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=hyperprolinémie de type I | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  786. hypoglycémie du nouveau-né --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=hypoglycémie du nouveau-né | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  787. hémoglobinurie d'effort --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=hémoglobinurie d'effort | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  788. isosthénurie --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=isosthénurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  789. maladie de surcharge --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=maladie de surcharge | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  790. microalbuminurie --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=microalbuminurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  791. mucolipidose II --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=mucolipidose II | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  792. oligophrénie --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=oligophrénie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  793. paridensité urinaire --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=paridensité urinaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  794. phénylcétonurie de type i --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=phénylcétonurie de type i | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  795. syndrome de Martin-Bell --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=syndrome de Martin-Bell | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  796. température corporelle élevée --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=température corporelle élevée | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  797. trisomie --- r_associated #0: 31 --> en:classical phenylketonuria
    n1=trisomie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=31
  798. Chopart (désarticulation de) --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=Chopart (désarticulation de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  799. Maladie héréditaire --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=Maladie héréditaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  800. acido-cétose --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=acido-cétose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  801. acidocétose --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=acidocétose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  802. acidoses lactiques (classification selon Cohen et Woods) --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=acidoses lactiques (classification selon Cohen et Woods) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  803. acrodermatite entéropathique --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=acrodermatite entéropathique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  804. adénite sinusale cytophagique --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=adénite sinusale cytophagique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  805. arriération --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=arriération | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  806. cétoacidose --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=cétoacidose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  807. déficit en cytochrome oxydase --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=déficit en cytochrome oxydase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  808. déficit en cytochrome-c oxydase --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=déficit en cytochrome-c oxydase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  809. en:17q11.2 microduplication syndrome --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:17q11.2 microduplication syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  810. en:Sydenham's chorea --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:Sydenham's chorea | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  811. en:acrodermatitis enteropathica --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:acrodermatitis enteropathica | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  812. en:additional sex chromosome --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:additional sex chromosome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  813. en:aminomethyltransferase deficiency --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:aminomethyltransferase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  814. en:ammoniuria --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:ammoniuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  815. en:anauxetic dysplasia --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:anauxetic dysplasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  816. en:and mental retardation --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:and mental retardation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  817. en:biliuria --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:biliuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  818. en:braddock syndrome --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:braddock syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  819. en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  820. en:charge syndrome --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:charge syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  821. en:cleft jaw --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:cleft jaw | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  822. en:cleft lip and palate --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:cleft lip and palate | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  823. en:cleft palate with cleft lip --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:cleft palate with cleft lip | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  824. en:congenital anomaly of the hematopoietic system --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:congenital anomaly of the hematopoietic system | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  825. en:congenital deformity of pinna --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:congenital deformity of pinna | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  826. en:congenital malformation of genital organs --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:congenital malformation of genital organs | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  827. en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  828. en:congenital red cell hypoplasia --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:congenital red cell hypoplasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  829. en:congenital transferrin deficiency --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:congenital transferrin deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  830. en:cytochrome-c oxidase deficiency --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:cytochrome-c oxidase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  831. en:deafness --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:deafness | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  832. en:developmental fault --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:developmental fault | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  833. en:developmental malformation of branchial arch --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:developmental malformation of branchial arch | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  834. en:dicarboxylicaminoaciduria --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:dicarboxylicaminoaciduria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  835. en:disorder due to n-acetyltransferase enzyme variant --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:disorder due to n-acetyltransferase enzyme variant | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  836. en:disorder of sulfur-bearing amino acid metabolism --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:disorder of sulfur-bearing amino acid metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  837. en:failure of the mind --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:failure of the mind | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  838. en:fanconi syndrome --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:fanconi syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  839. en:fronto-facio-nasal dysplasia --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:fronto-facio-nasal dysplasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  840. en:funguria --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:funguria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  841. en:glutamate-cysteine ligase deficiency --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:glutamate-cysteine ligase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  842. en:glutaric aciduria type 1 --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:glutaric aciduria type 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  843. en:glycogen storage disease type x --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:glycogen storage disease type x | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  844. en:gurrieri sammito bellussi syndrome --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:gurrieri sammito bellussi syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  845. en:hand and foot deformity --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:hand and foot deformity | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  846. en:hemolytic anemia due to pyruvate kinase deficiency --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:hemolytic anemia due to pyruvate kinase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  847. en:hereditary factor xii deficiency disease --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:hereditary factor xii deficiency disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  848. en:hydrocephalus --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:hydrocephalus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  849. en:hyperchloruria --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:hyperchloruria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  850. en:hyperimmunoglobulin e syndrome --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:hyperimmunoglobulin e syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  851. en:hyperlipoproteinemia type i --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:hyperlipoproteinemia type i | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  852. en:hyperphenylalaninemia, bh4-deficient, b --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:hyperphenylalaninemia, bh4-deficient, b | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  853. en:hyperphosphatasia with mental retardation --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:hyperphosphatasia with mental retardation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  854. en:inborn error of lipoprotein metabolism --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:inborn error of lipoprotein metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  855. en:isaacs syndrome --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:isaacs syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  856. en:jankovic rivera syndrome --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:jankovic rivera syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  857. en:ketoacidosis --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:ketoacidosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  858. en:learning disability --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:learning disability | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  859. en:lethal congenital contracture syndrome 2 --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:lethal congenital contracture syndrome 2 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  860. en:mental handicap --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:mental handicap | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  861. en:muscle l-lactate dehydrogenase deficiency --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:muscle l-lactate dehydrogenase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  862. en:naxos disease --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:naxos disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  863. en:neurodevelopmental anomaly --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:neurodevelopmental anomaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  864. en:niemann-pick disease --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:niemann-pick disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  865. en:other congenital malformations of digestive system --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:other congenital malformations of digestive system | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  866. en:other disturbances of straight-chain amino-acid metabolism --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:other disturbances of straight-chain amino-acid metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  867. en:pelviscapular dysplasia --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:pelviscapular dysplasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  868. en:porphyrinuria --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:porphyrinuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  869. en:pyloric obstruction --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:pyloric obstruction | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  870. en:pyloric stenosis --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:pyloric stenosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  871. en:renal dysplasia - limb defects syndrome --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:renal dysplasia - limb defects syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  872. en:retardation --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:retardation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  873. en:single congenital anomaly --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:single congenital anomaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  874. en:sitosterolemia with xanthomatosis --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:sitosterolemia with xanthomatosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  875. en:sonoda syndrome --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:sonoda syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  876. en:spondyloenchondrodysplasia with immune dysregulation --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:spondyloenchondrodysplasia with immune dysregulation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  877. en:spondyloepiphyseal dysplasia tarda, toledo type --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:spondyloepiphyseal dysplasia tarda, toledo type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  878. en:strabismus syndrome --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:strabismus syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  879. en:thyroid dyshormonogenesis 4 --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:thyroid dyshormonogenesis 4 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  880. en:transcobalamin ii deficiency --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:transcobalamin ii deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  881. en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  882. en:wolf-hirschhorn syndrome --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:wolf-hirschhorn syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  883. en:x-linked intellectual disability stoll type --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=en:x-linked intellectual disability stoll type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  884. hyperperméabilité capillaire (syndrome d') --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=hyperperméabilité capillaire (syndrome d') | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  885. hypopituitarisme --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=hypopituitarisme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  886. jumeaux conjoints --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=jumeaux conjoints | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  887. maladie de Tay-Sachs --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=maladie de Tay-Sachs | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  888. maladie de fölling --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=maladie de fölling | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  889. maladie de marchiafava-micheli --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=maladie de marchiafava-micheli | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  890. sténose du pylore --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=sténose du pylore | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  891. sténose pylorique --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=sténose pylorique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  892. syndrome de la marionnette joyeuse --- r_associated #0: 30 --> en:classical phenylketonuria
    n1=syndrome de la marionnette joyeuse | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
  893. brides amniotiques (syndrome des) --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=brides amniotiques (syndrome des) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  894. cataracte-atrophie du cervelet-myopathie --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=cataracte-atrophie du cervelet-myopathie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  895. déficit grave en phénylalanine hydroxylase --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=déficit grave en phénylalanine hydroxylase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  896. en:absent corpus callosum --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:absent corpus callosum | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  897. en:adenylosuccinate lyase deficiency (disorder) --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:adenylosuccinate lyase deficiency (disorder) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  898. en:agenesis --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:agenesis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  899. en:aicardi syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:aicardi syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  900. en:alkaptonuria --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:alkaptonuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  901. en:alpha-1 antitrypsin deficiency --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:alpha-1 antitrypsin deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  902. en:alpha-methylacyl-coa racemase deficiency --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:alpha-methylacyl-coa racemase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  903. en:amino acid metabolism disorder --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:amino acid metabolism disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  904. en:anal imperforation --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:anal imperforation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  905. en:and microgenitalism --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:and microgenitalism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  906. en:aniridia and intellectual disability syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:aniridia and intellectual disability syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  907. en:ataxia with vitamin e deficiency --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:ataxia with vitamin e deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  908. en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  909. en:autosomal recessive idiopathic familial dystonia --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:autosomal recessive idiopathic familial dystonia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  910. en:autosomal recessive muscular dystrophy with limb girdle distribution --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:autosomal recessive muscular dystrophy with limb girdle distribution | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  911. en:bisphosphoglycerate mutase deficiency --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:bisphosphoglycerate mutase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  912. en:brain diseases, metabolic, inborn --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:brain diseases, metabolic, inborn | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  913. en:cleft lip/palate-ectodermal dysplasia syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:cleft lip/palate-ectodermal dysplasia syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  914. en:cleft maxilla --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:cleft maxilla | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  915. en:congenital deformity of hip --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:congenital deformity of hip | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  916. en:congenital deformity of knee joint --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:congenital deformity of knee joint | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  917. en:congenital deformity of mitral valve annulus --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:congenital deformity of mitral valve annulus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  918. en:congenital disorder of glycosylation type id --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:congenital disorder of glycosylation type id | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  919. en:congenital disorder of glycosylation type ie --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:congenital disorder of glycosylation type ie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  920. en:congenital malformation syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:congenital malformation syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  921. en:craniostenosis --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:craniostenosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  922. en:cutaneous photosensitivity and lethal colitis syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:cutaneous photosensitivity and lethal colitis syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  923. en:disorder characterized by fever --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:disorder characterized by fever | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  924. en:disorder due to cytochrome p450 enzyme variant --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:disorder due to cytochrome p450 enzyme variant | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  925. en:disorder of amino acid and organic acid metabolism --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:disorder of amino acid and organic acid metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  926. en:disorder of pyruvate metabolism and mitochondrial respiratory chain --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:disorder of pyruvate metabolism and mitochondrial respiratory chain | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  927. en:disorder of tryptophan metabolism --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:disorder of tryptophan metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  928. en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  929. en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  930. en:embryonic cyst --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:embryonic cyst | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  931. en:exertional hemoglobinuria --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:exertional hemoglobinuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  932. en:female restricted epilepsy with intellectual disability syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:female restricted epilepsy with intellectual disability syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  933. en:gaucher disease --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:gaucher disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  934. en:glutamate formiminotransferase deficiency --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:glutamate formiminotransferase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  935. en:hereditary hyperbilirubinemia --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:hereditary hyperbilirubinemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  936. en:hereditary methemoglobinemia, enzymatic type --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:hereditary methemoglobinemia, enzymatic type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  937. en:hereditary spastic paralysis, infantile onset ascending --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:hereditary spastic paralysis, infantile onset ascending | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  938. en:hnsha due to glutathione reductase deficiency --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:hnsha due to glutathione reductase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  939. en:hnsha due to pyrimidine-5'-nucleotidase deficiency --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  940. en:homocystinemia --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:homocystinemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  941. en:hypermanganesemia with dystonia polycythemia and cirrhosis --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:hypermanganesemia with dystonia polycythemia and cirrhosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  942. en:hypothalamic hamartoblastoma --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:hypothalamic hamartoblastoma | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  943. en:inborn errors of steroid synthesis --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:inborn errors of steroid synthesis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  944. en:increased aromatase activity --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:increased aromatase activity | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  945. en:inherited disease --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:inherited disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  946. en:laron syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:laron syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  947. en:leukotriene c4 synthase deficiency --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:leukotriene c4 synthase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  948. en:lipoid congenital adrenal hyperplasia --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:lipoid congenital adrenal hyperplasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  949. en:lissencephaly type 3 familial fetal akinesia sequence syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  950. en:macdermot winter syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:macdermot winter syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  951. en:majeed syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:majeed syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  952. en:mental retardation syndrome, belgian type --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:mental retardation syndrome, belgian type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  953. en:methylmalonic aciduria --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:methylmalonic aciduria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  954. en:microcephalic primordial dwarfism toriello type --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:microcephalic primordial dwarfism toriello type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  955. en:mitochondrial dna depletion syndrome 2 (myopathic type) --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:mitochondrial dna depletion syndrome 2 (myopathic type) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  956. en:monopia --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:monopia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  957. en:muscle amp deaminase deficiency --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:muscle amp deaminase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  958. en:najjar syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:najjar syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  959. en:north american indian childhood cirrhosis --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:north american indian childhood cirrhosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  960. en:ornithine carbamoyltransferase deficiency disease --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  961. en:other disorders of aromatic amino-acid metabolism --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:other disorders of aromatic amino-acid metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  962. en:other specified disorders of amino-acid transport and metabolism --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:other specified disorders of amino-acid transport and metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  963. en:pelizaeus merzbacher like disease --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:pelizaeus merzbacher like disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  964. en:peroxisomal disorder --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:peroxisomal disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  965. en:piussan lenaerts mathieu syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:piussan lenaerts mathieu syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  966. en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  967. en:porphyruria --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:porphyruria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  968. en:pyridoxine dependency syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:pyridoxine dependency syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  969. en:recurrent hypoglycemia --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:recurrent hypoglycemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  970. en:sanfilippo syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:sanfilippo syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  971. en:savant syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:savant syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  972. en:spastic paraplegia 15, autosomal recessive --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:spastic paraplegia 15, autosomal recessive | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  973. en:tetrahydrobiopterin synthesis defect --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:tetrahydrobiopterin synthesis defect | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  974. en:traumatic hematuria --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:traumatic hematuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  975. en:trichohepatoenteric syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:trichohepatoenteric syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  976. en:tungland bellman syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:tungland bellman syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  977. en:tyrosinemia --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:tyrosinemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  978. en:verloes bourguignon syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:verloes bourguignon syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  979. en:waisman syndrome --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=en:waisman syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  980. exéma --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=exéma | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  981. petite taille, hyperextensibilité, hernie et dépression oculaire --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=petite taille, hyperextensibilité, hernie et dépression oculaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  982. phénylcétonuries --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=phénylcétonuries | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  983. situs mutatus --- r_associated #0: 29 --> en:classical phenylketonuria
    n1=situs mutatus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=29
  984. Maladie de Tay-Sachs --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=Maladie de Tay-Sachs | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  985. déficit congénital en mégacaryocytes --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=déficit congénital en mégacaryocytes | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  986. en:2-hydroxyglutaric aciduria --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:2-hydroxyglutaric aciduria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  987. en:Angelman's syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:Angelman's syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  988. en:Dubin-Sprinz disease --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:Dubin-Sprinz disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  989. en:Leroy's i-cell disease --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:Leroy's i-cell disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  990. en:acephalostomia --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:acephalostomia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  991. en:acrorenal mandibular syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:acrorenal mandibular syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  992. en:arachnodactyly and intellectual disability with facial dysmorphism syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:arachnodactyly and intellectual disability with facial dysmorphism syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  993. en:atrophoderma vermiculatum --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:atrophoderma vermiculatum | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  994. en:bilirubinuria --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:bilirubinuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  995. en:brown-vialetto-van laere syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:brown-vialetto-van laere syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  996. en:bulbus cordis anomalies and anomalies of cardiac septal closure --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:bulbus cordis anomalies and anomalies of cardiac septal closure | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  997. en:cebocephaly --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:cebocephaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  998. en:celosomy --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:celosomy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  999. en:certain congenital musculoskeletal deformities --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:certain congenital musculoskeletal deformities | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1000. en:citrin deficiency --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:citrin deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1001. en:complete trisomy 18 syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:complete trisomy 18 syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1002. en:congenital anomaly of face --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:congenital anomaly of face | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1003. en:congenital cardiovascular abnormality --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:congenital cardiovascular abnormality | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1004. en:congenital disorder of glycosylation type ic --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:congenital disorder of glycosylation type ic | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1005. en:congenital disorder of glycosylation, type if --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:congenital disorder of glycosylation, type if | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1006. en:congenital foot deformity --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:congenital foot deformity | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1007. en:congenital hand and foot deformity --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:congenital hand and foot deformity | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1008. en:congenital leptin deficiency --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:congenital leptin deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1009. en:congenital macrocephaly --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:congenital macrocephaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1010. en:congenital pancreatic enterokinase deficiency --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:congenital pancreatic enterokinase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1011. en:connatal disorder --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:connatal disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1012. en:corpus callosum agenesis neuronopathy --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:corpus callosum agenesis neuronopathy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1013. en:craniofacial ulnar renal syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:craniofacial ulnar renal syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1014. en:deafness and myopia syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:deafness and myopia syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1015. en:deafness, congenital, with inner ear agenesis, microtia, and microdontia --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1016. en:deficiency in enzyme complexes of mitochondrial respiratory chain --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:deficiency in enzyme complexes of mitochondrial respiratory chain | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1017. en:dihydropyrimidine dehydrogenase deficiency --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:dihydropyrimidine dehydrogenase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1018. en:ehlers-danlos syndrome, type vi --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:ehlers-danlos syndrome, type vi | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1019. en:emanuel syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:emanuel syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1020. en:epiphyseal dysplasia, multiple, 4 --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:epiphyseal dysplasia, multiple, 4 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1021. en:familial hypoaldosteronism --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:familial hypoaldosteronism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1022. en:familial median cleft of upper and lower lip --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:familial median cleft of upper and lower lip | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1023. en:fried syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:fried syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1024. en:geroderma osteodysplastica --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:geroderma osteodysplastica | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1025. en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1026. en:harrod doman keele syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:harrod doman keele syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1027. en:hmg-coa lyase deficiency --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:hmg-coa lyase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1028. en:hyperphenylalaninaemia --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:hyperphenylalaninaemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1029. en:idiot --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:idiot | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1030. en:inborn errors of metabolism nec in cst95 --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:inborn errors of metabolism nec in cst95 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1031. en:infection causing congenital anomaly --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:infection causing congenital anomaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1032. en:insulin growth factor i deficiency --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:insulin growth factor i deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1033. en:intellectual disability --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:intellectual disability | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1034. en:intermediary metabolism disorder --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:intermediary metabolism disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1035. en:jervell and lange nielsen syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:jervell and lange nielsen syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1036. en:kabuki syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:kabuki syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1037. en:kohlschutter tonz syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:kohlschutter tonz syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1038. en:kosztolanyi syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:kosztolanyi syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1039. en:lactase deficiency, congenital --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:lactase deficiency, congenital | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1040. en:lipid metabolism, inborn errors --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:lipid metabolism, inborn errors | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1041. en:malignant hyperthermia syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:malignant hyperthermia syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1042. en:mannosidosis --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:mannosidosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1043. en:march hemoglobinuria --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:march hemoglobinuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1044. en:megaloglossia --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:megaloglossia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1045. en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1046. en:microphthalmia, syndromic 4 (disorder) --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:microphthalmia, syndromic 4 (disorder) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1047. en:miller-mckusick-malvaux-syndrome (3m syndrome) --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:miller-mckusick-malvaux-syndrome (3m syndrome) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1048. en:multiple sulfatase deficiency disease --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:multiple sulfatase deficiency disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1049. en:n-acetylglutamate synthase deficiency --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:n-acetylglutamate synthase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1050. en:nathalie syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:nathalie syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1051. en:neonatal disorder --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:neonatal disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1052. en:neurodegeneration due to cerebral folate transport deficiency --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:neurodegeneration due to cerebral folate transport deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1053. en:nicolaides baraitser syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:nicolaides baraitser syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1054. en:normal sweating --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:normal sweating | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1055. en:normalization of metabolic parameters in between crises --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:normalization of metabolic parameters in between crises | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1056. en:oculocerebral hypopigmentation syndrome type preus --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:oculocerebral hypopigmentation syndrome type preus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1057. en:papillon-lefevre syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:papillon-lefevre syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1058. en:pediatric terminology --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:pediatric terminology | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1059. en:peeling skin syndrome, acral type --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:peeling skin syndrome, acral type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1060. en:phenylketonuria screening test --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:phenylketonuria screening test | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1061. en:porphobilinogen synthase deficiency --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:porphobilinogen synthase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1062. en:presentey anomaly --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:presentey anomaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1063. en:prickle1-related progressive myoclonus epilepsy with ataxia --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:prickle1-related progressive myoclonus epilepsy with ataxia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1064. en:primary immunodeficiency syndrome due to p14 deficiency --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1065. en:proctatresia --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:proctatresia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1066. en:rapadilino syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:rapadilino syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1067. en:reardon hall slaney syndrome --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:reardon hall slaney syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1068. en:rna polymerase iii-related leukodystrophy --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:rna polymerase iii-related leukodystrophy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1069. en:spinocerebellar ataxia, autosomal recessive 2 --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:spinocerebellar ataxia, autosomal recessive 2 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1070. en:spondyloenchondrodysplasia --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:spondyloenchondrodysplasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1071. en:stomatognathic system abnormalities --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:stomatognathic system abnormalities | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1072. en:thyroid dysgenesis --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:thyroid dysgenesis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1073. en:unspecified mental retardation; without mention of impairment of behaviour --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:unspecified mental retardation; without mention of impairment of behaviour | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1074. en:valinemia --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:valinemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1075. en:vrozené poruchy metabolismu nec in mdrcze18_1 --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:vrozené poruchy metabolismu nec in mdrcze18_1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1076. en:x-linked intellectual disability cantagrel type --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=en:x-linked intellectual disability cantagrel type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1077. fente palatine --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=fente palatine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1078. malformation --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=malformation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1079. syndrome de Zellweger --- r_associated #0: 28 --> en:classical phenylketonuria
    n1=syndrome de Zellweger | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  1080. BEC DE LIEVRE --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=BEC DE LIEVRE | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1081. TPN ou NADP --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=TPN ou NADP | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1082. en:Lowe's syndrome --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:Lowe's syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1083. en:abnormal urine --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:abnormal urine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1084. en:abnormality, severe teratoid --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:abnormality, severe teratoid | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1085. en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1086. en:alpha, alpha-trehalase deficiency --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:alpha, alpha-trehalase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1087. en:amegakaryocytic thrombocytopenia with congenital malformation --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:amegakaryocytic thrombocytopenia with congenital malformation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1088. en:amino acid deficiency --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:amino acid deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1089. en:anomaly congenital special senses --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:anomaly congenital special senses | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1090. en:ataxia telangiectasia syndrome --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:ataxia telangiectasia syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1091. en:ateliotic dwarfism without insulinopenia --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:ateliotic dwarfism without insulinopenia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1092. en:autosomal recessive spastic paraplegia type 11 --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:autosomal recessive spastic paraplegia type 11 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1093. en:behr syndrome --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:behr syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1094. en:circulating enzyme deficiency --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:circulating enzyme deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1095. en:congenital deformity of ankle joint --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:congenital deformity of ankle joint | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1096. en:congenital deformity of chest wall --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:congenital deformity of chest wall | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1097. en:congenital dyserythropoietic anemia, type i --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:congenital dyserythropoietic anemia, type i | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1098. en:congenital dyserythropoietic anemia, type ii --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:congenital dyserythropoietic anemia, type ii | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1099. en:congenital dysplasia --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:congenital dysplasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1100. en:congenital keratoglobus --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:congenital keratoglobus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1101. en:congenital septation --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:congenital septation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1102. en:congenital sucrase-isomaltase deficiency --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:congenital sucrase-isomaltase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1103. en:congenital visceral anomaly --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:congenital visceral anomaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1104. en:cranioschisis --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:cranioschisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1105. en:cri du chat syndrome --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:cri du chat syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1106. en:crigler-najjar syndrome --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:crigler-najjar syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1107. en:cryptophthalmos syndrome --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:cryptophthalmos syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1108. en:delayed epiphyseal fusion --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:delayed epiphyseal fusion | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1109. en:desmosterolosis --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:desmosterolosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1110. en:ehlers-danlos syndrome kyphoscoliotic and deafness type --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1111. en:excretion of dicarboxylic acids --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:excretion of dicarboxylic acids | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1112. en:faecaluria --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:faecaluria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1113. en:familial renal iminoglycinuria --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:familial renal iminoglycinuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1114. en:feeble-mindedness --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:feeble-mindedness | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1115. en:fryns macrocephaly --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:fryns macrocephaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1116. en:generalized hypopigmentation --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:generalized hypopigmentation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1117. en:greig syndrome --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:greig syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1118. en:heat-stroke --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:heat-stroke | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1119. en:holocarboxylase synthetase deficiency --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:holocarboxylase synthetase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1120. en:hypercholesterolemia (disorder) --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:hypercholesterolemia (disorder) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1121. en:hyperkaliuria --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:hyperkaliuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1122. en:hyperornithinemia --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:hyperornithinemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1123. en:hyperphenylalaninemia --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:hyperphenylalaninemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1124. en:hyperprolinemia --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:hyperprolinemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1125. en:hyperthermy --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:hyperthermy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1126. en:hypoglycaemic episode --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:hypoglycaemic episode | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1127. en:hypomagnesemia 1, intestinal --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:hypomagnesemia 1, intestinal | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1128. en:hypophosphatemic rickets with hypercalciuria, hereditary --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:hypophosphatemic rickets with hypercalciuria, hereditary | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1129. en:impairment of urinary concentration --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:impairment of urinary concentration | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1130. en:inborn errors of porphyrin metabolism --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:inborn errors of porphyrin metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1131. en:kallman syndrome with heart disease --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:kallman syndrome with heart disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1132. en:macular corneal dystrophy --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:macular corneal dystrophy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1133. en:major congenital anomaly --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:major congenital anomaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1134. en:manouvrier syndrome --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:manouvrier syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1135. en:marles greenberg persaud syndrome --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:marles greenberg persaud syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1136. en:microcephaly, amish type (disorder) --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:microcephaly, amish type (disorder) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1137. en:mild mental retardation --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:mild mental retardation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1138. en:multiple acyl-coa dehydrogenase deficiency --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:multiple acyl-coa dehydrogenase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1139. en:myopathy, early-onset, with fatal cardiomyopathy --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:myopathy, early-onset, with fatal cardiomyopathy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1140. en:netherton syndrome --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:netherton syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1141. en:neuroacanthocytosis --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:neuroacanthocytosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1142. en:phenylalanine-free diet education --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:phenylalanine-free diet education | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1143. en:phenylketonuria ii --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:phenylketonuria ii | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1144. en:prosoposchisis --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:prosoposchisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1145. en:purine-nucleoside phosphorylase deficiency --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:purine-nucleoside phosphorylase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1146. en:severe early childhood onset retinal dystrophy --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:severe early childhood onset retinal dystrophy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1147. en:sudden infant death with dysgenesis of the testes syndrome --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:sudden infant death with dysgenesis of the testes syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1148. en:sulfite oxidase deficiency --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:sulfite oxidase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1149. en:trisomy --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:trisomy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1150. en:trisomy 14 --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:trisomy 14 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1151. en:urine microscopy leukocytes present finding --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:urine microscopy leukocytes present finding | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1152. en:uroglycosis --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:uroglycosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1153. en:x-linked intellectual disability pai type --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:x-linked intellectual disability pai type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1154. en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1155. en:zinc-deficiency type --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=en:zinc-deficiency type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1156. hyperprolinémie --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=hyperprolinémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1157. maladie de dubin-johnson --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=maladie de dubin-johnson | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1158. neuro-acanthocytose --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=neuro-acanthocytose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1159. pied-bot --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=pied-bot | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1160. semialdéhyde succinique-déshydrogénase (déficit en) --- r_associated #0: 27 --> en:classical phenylketonuria
    n1=semialdéhyde succinique-déshydrogénase (déficit en) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  1161. Déficience intellectuelle --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=Déficience intellectuelle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1162. acidurie mévalonique --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=acidurie mévalonique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1163. bébé bronzé (syndrome du) --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=bébé bronzé (syndrome du) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1164. communication inter-auriculaire --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=communication inter-auriculaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1165. communication interauriculaire --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=communication interauriculaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1166. cristallurie --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=cristallurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1167. cétoacidurie à chaînes ramifiées --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=cétoacidurie à chaînes ramifiées | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1168. division palatine --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=division palatine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1169. dysplasie craniodiaphysaire --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=dysplasie craniodiaphysaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1170. en:3-methylglutaconic aciduria type 3 --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:3-methylglutaconic aciduria type 3 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1171. en:Dubin-Johnson's syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:Dubin-Johnson's syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1172. en:Gaucher disease --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:Gaucher disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1173. en:abnormal fetal duplication --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:abnormal fetal duplication | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1174. en:acid phosphatase deficiency --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:acid phosphatase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1175. en:acquired lactase deficiency --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:acquired lactase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1176. en:acrocallosal syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:acrocallosal syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1177. en:anemia, hypochromic microcytic, with iron overload --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:anemia, hypochromic microcytic, with iron overload | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1178. en:arthrogryposis multiplex congenita, neurogenic type (disorder) --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1179. en:autosomal recessive primary microcephaly --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:autosomal recessive primary microcephaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1180. en:autosomal recessive sideroblastic anemia --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:autosomal recessive sideroblastic anemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1181. en:bardet-biedl syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:bardet-biedl syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1182. en:beta-methylcrotonylglycinuria --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:beta-methylcrotonylglycinuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1183. en:bowen-conradi syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:bowen-conradi syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1184. en:candiduria --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:candiduria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1185. en:cardiovascular abnormalities --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:cardiovascular abnormalities | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1186. en:cerebellar ataxia ectodermal dysplasia --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:cerebellar ataxia ectodermal dysplasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1187. en:cerebroretinal microangiopathy with calcifications and cysts (disorder) --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1188. en:charcot-marie-tooth disease type 4 --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:charcot-marie-tooth disease type 4 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1189. en:childhood myocerebrohepatopathy spectrum --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:childhood myocerebrohepatopathy spectrum | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1190. en:chitty hall baraitser syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:chitty hall baraitser syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1191. en:coffin-siris syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:coffin-siris syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1192. en:cohen syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:cohen syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1193. en:congenital anomaly of neck --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:congenital anomaly of neck | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1194. en:congenital stenosis --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:congenital stenosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1195. en:conjoined twins --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:conjoined twins | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1196. en:craniodiaphyseal dysplasia --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:craniodiaphyseal dysplasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1197. en:cryoglobulinuria --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:cryoglobulinuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1198. en:cryptophthalmia --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:cryptophthalmia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1199. en:crystalluria --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:crystalluria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1200. en:cystathionine beta-synthase deficiency disease --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:cystathionine beta-synthase deficiency disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1201. en:cystinosis --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:cystinosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1202. en:developmental stricture --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:developmental stricture | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1203. en:disorder of lysine and hydroxylysine metabolism --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:disorder of lysine and hydroxylysine metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1204. en:dwarfism --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:dwarfism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1205. en:dysmorphism --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:dysmorphism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1206. en:elevated alkaline phosphatase --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:elevated alkaline phosphatase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1207. en:exumbilication --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:exumbilication | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1208. en:fibular hypoplasia and complex brachydactyly --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:fibular hypoplasia and complex brachydactyly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1209. en:folinic acid responsive seizure syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:folinic acid responsive seizure syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1210. en:glucose-6-phosphate dehydrogenase deficiency anemia --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:glucose-6-phosphate dehydrogenase deficiency anemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1211. en:glutathione s-transferase deficiency --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:glutathione s-transferase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1212. en:hereditary palmoplantar keratoderma gamborg nielsen type --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:hereditary palmoplantar keratoderma gamborg nielsen type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1213. en:hydroxyprolinemia --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:hydroxyprolinemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1214. en:hyperandrogenism due to non-classic 21-hydroxylase deficiency --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:hyperandrogenism due to non-classic 21-hydroxylase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1215. en:hyperprolinemia type 1 --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:hyperprolinemia type 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1216. en:hypomyelination and congenital cataract --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:hypomyelination and congenital cataract | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1217. en:hypopituitarism --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:hypopituitarism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1218. en:inherited disorder of folate metabolism --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:inherited disorder of folate metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1219. en:isolated hypoplasia of the right ventricle --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:isolated hypoplasia of the right ventricle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1220. en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1221. en:lymphatic abnormalities --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:lymphatic abnormalities | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1222. en:lysinuric protein intolerance --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:lysinuric protein intolerance | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1223. en:megalencephalic leukoencephalopathy with subcortical cysts --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:megalencephalic leukoencephalopathy with subcortical cysts | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1224. en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1225. en:methionine adenosyltransferase deficiency --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:methionine adenosyltransferase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1226. en:morquio syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:morquio syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1227. en:mowat-wilson syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:mowat-wilson syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1228. en:myoglobinuria, recurrent --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:myoglobinuria, recurrent | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1229. en:neonatal jaundice --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:neonatal jaundice | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1230. en:normal blood lactate levels (in both patients) --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:normal blood lactate levels (in both patients) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1231. en:norrie syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:norrie syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1232. en:northern epilepsy syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:northern epilepsy syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1233. en:opitz trigonocephaly syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:opitz trigonocephaly syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1234. en:oxalosis --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:oxalosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1235. en:persistent mullerian duct syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:persistent mullerian duct syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1236. en:photomyoclonus --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:photomyoclonus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1237. en:premature aging syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:premature aging syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1238. en:pseudohypoaldosteronism, type 1, recessive form --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:pseudohypoaldosteronism, type 1, recessive form | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1239. en:pterygium colli syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:pterygium colli syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1240. en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1241. en:pyruvate dehydrogenase deficiency --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:pyruvate dehydrogenase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1242. en:renal aminoacidurias --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:renal aminoacidurias | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1243. en:renal tubulopathy with encephalopathy and liver failure syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:renal tubulopathy with encephalopathy and liver failure syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1244. en:robinow-like syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:robinow-like syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1245. en:saito kuba tsuruta syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:saito kuba tsuruta syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1246. en:scholte syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:scholte syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1247. en:sly syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:sly syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1248. en:specific enzyme deficiency --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:specific enzyme deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1249. en:spinocerebellar ataxia with epilepsy --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:spinocerebellar ataxia with epilepsy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1250. en:thomas syndrome --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:thomas syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1251. en:tmem70 related mitochondrial encephalo-cardio-myopathy --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:tmem70 related mitochondrial encephalo-cardio-myopathy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1252. en:trisomy 10p --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:trisomy 10p | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1253. en:ugt1a1*28 polymorphism --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:ugt1a1*28 polymorphism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1254. en:x-linked intellectual disability miles carpenter type --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:x-linked intellectual disability miles carpenter type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1255. en:x-linked intellectual disability van esch type --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=en:x-linked intellectual disability van esch type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1256. hydroxyprolinémie --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=hydroxyprolinémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1257. jumeaux fusionnés --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=jumeaux fusionnés | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1258. jumeaux siamois --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=jumeaux siamois | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1259. pcu --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=pcu | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1260. phénylcétonurie classique --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=phénylcétonurie classique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1261. syndrome progéroïde de de barsy --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=syndrome progéroïde de de barsy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1262. troubles endocriniens, épilepsie et déficience mentale --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=troubles endocriniens, épilepsie et déficience mentale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1263. télécanthus --- r_associated #0: 26 --> en:classical phenylketonuria
    n1=télécanthus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  1264. albinisme avec pigmentation minime --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=albinisme avec pigmentation minime | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1265. en:Siamese twins --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=en:Siamese twins | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1266. en:X-linked --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=en:X-linked | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1267. en:hereditary illness --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=en:hereditary illness | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1268. en:histidinaemia --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=en:histidinaemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1269. en:hypophosphatasia --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=en:hypophosphatasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1270. en:juvenile cataract --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=en:juvenile cataract | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1271. en:nystagmus --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=en:nystagmus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1272. en:oligergasia --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=en:oligergasia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1273. en:oligopsychia --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=en:oligopsychia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1274. en:phenylalanine hydroxylase --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=en:phenylalanine hydroxylase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1275. en:type a 14 --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=en:type a 14 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1276. en:ureorrhea --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=en:ureorrhea | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1277. en:wolman's disease --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=en:wolman's disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1278. frères siamois --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=frères siamois | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1279. insuffisance staturale --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=insuffisance staturale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1280. kératocône posticus --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=kératocône posticus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1281. myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1282. syndrome hétérotaxique --- r_associated #0: 25 --> en:classical phenylketonuria
    n1=syndrome hétérotaxique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=25
  1283. acrodermatitis enteropathica --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=acrodermatitis enteropathica | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1284. albinisme oculocutané de type mutant jaune --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=albinisme oculocutané de type mutant jaune | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1285. contractures congénitales et arachnodactylie --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=contractures congénitales et arachnodactylie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1286. en:cerebellar atrophy --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=en:cerebellar atrophy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1287. en:chromosomal aberration --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=en:chromosomal aberration | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1288. en:congenital functional anomaly --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=en:congenital functional anomaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1289. en:fervescence --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=en:fervescence | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1290. en:heart ectopy --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=en:heart ectopy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1291. en:hematomphalus --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=en:hematomphalus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1292. en:hydruria --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=en:hydruria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1293. en:morosis --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=en:morosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1294. en:type I --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=en:type I | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1295. en:umbilical hiatus --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=en:umbilical hiatus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1296. en:urophtisis --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=en:urophtisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1297. glycogénose --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=glycogénose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1298. sclérodermie tubéreuse de bourneville --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=sclérodermie tubéreuse de bourneville | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1299. syndrome de lowe --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=syndrome de lowe | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1300. triskélion --- r_associated #0: 24 --> en:classical phenylketonuria
    n1=triskélion | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=24
  1301. albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception --- r_associated #0: 23 --> en:classical phenylketonuria
    n1=albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23
  1302. communication interventriculaire --- r_associated #0: 23 --> en:classical phenylketonuria
    n1=communication interventriculaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23
  1303. en:Folling's disease --- r_associated #0: 23 --> en:classical phenylketonuria
    n1=en:Folling's disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23
  1304. en:Martin-Bell's syndrome --- r_associated #0: 23 --> en:classical phenylketonuria
    n1=en:Martin-Bell's syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23
  1305. en:Nathalie syndrome --- r_associated #0: 23 --> en:classical phenylketonuria
    n1=en:Nathalie syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23
  1306. en:biliary atresia --- r_associated #0: 23 --> en:classical phenylketonuria
    n1=en:biliary atresia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23
  1307. en:congenital genitourinary abnormality --- r_associated #0: 23 --> en:classical phenylketonuria
    n1=en:congenital genitourinary abnormality | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23
  1308. en:diaphragmatic hernia --- r_associated #0: 23 --> en:classical phenylketonuria
    n1=en:diaphragmatic hernia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23
  1309. en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) --- r_associated #0: 23 --> en:classical phenylketonuria
    n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23
  1310. en:sphingolipidosis --- r_associated #0: 23 --> en:classical phenylketonuria
    n1=en:sphingolipidosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23
  1311. en:with growth retardation --- r_associated #0: 23 --> en:classical phenylketonuria
    n1=en:with growth retardation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23
  1312. maladie de roger --- r_associated #0: 23 --> en:classical phenylketonuria
    n1=maladie de roger | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23
  1313. xanthique (lithiase) --- r_associated #0: 23 --> en:classical phenylketonuria
    n1=xanthique (lithiase) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23
  1314. Maladie de Wolman --- r_associated #0: 22 --> en:classical phenylketonuria
    n1=Maladie de Wolman | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=22
  1315. atrésie laryngée --- r_associated #0: 22 --> en:classical phenylketonuria
    n1=atrésie laryngée | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=22
  1316. cranioschisis --- r_associated #0: 22 --> en:classical phenylketonuria
    n1=cranioschisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=22
  1317. en:Laurence-Moon's syndrome --- r_associated #0: 22 --> en:classical phenylketonuria
    n1=en:Laurence-Moon's syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=22
  1318. en:and cerebellar ataxia due to duplication of mitochondrial DNA --- r_associated #0: 22 --> en:classical phenylketonuria
    n1=en:and cerebellar ataxia due to duplication of mitochondrial DNA | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=22
  1319. en:hyperlipoproteinemia --- r_associated #0: 22 --> en:classical phenylketonuria
    n1=en:hyperlipoproteinemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=22
  1320. en:hyperlipoproteinemia type I --- r_associated #0: 22 --> en:classical phenylketonuria
    n1=en:hyperlipoproteinemia type I | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=22
  1321. en:inborn immunodeficiency --- r_associated #0: 22 --> en:classical phenylketonuria
    n1=en:inborn immunodeficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=22
  1322. en:phenylketonuria (PKU) --- r_associated #0: 22 --> en:classical phenylketonuria
    n1=en:phenylketonuria (PKU) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=22
  1323. en:tyrosinemia type II --- r_associated #0: 22 --> en:classical phenylketonuria
    n1=en:tyrosinemia type II | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=22
  1324. hématurie --- r_associated #0: 22 --> en:classical phenylketonuria
    n1=hématurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=22
  1325. maladie du cri du chat --- r_associated #0: 22 --> en:classical phenylketonuria
    n1=maladie du cri du chat | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=22
  1326. palais fendu --- r_associated #0: 22 --> en:classical phenylketonuria
    n1=palais fendu | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=22
  1327. syndrome de Williams --- r_associated #0: 22 --> en:classical phenylketonuria
    n1=syndrome de Williams | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=22
  1328. acidurie argininosuccinique --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=acidurie argininosuccinique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1329. acidémie isovalérique --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=acidémie isovalérique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1330. alcaptonurie --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=alcaptonurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1331. ammoniurie --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=ammoniurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1332. argininémie --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=argininémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1333. candidurie --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=candidurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1334. cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1335. colobome de l'iris avec ptosis, hypertélorisme et retard mental --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=colobome de l'iris avec ptosis, hypertélorisme et retard mental | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1336. cystinurie --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=cystinurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1337. dyslipémie --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=dyslipémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1338. déficience mentale --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=déficience mentale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1339. déficit en biotinidase --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=déficit en biotinidase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1340. déficit en sulfite-oxydase --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=déficit en sulfite-oxydase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1341. déficit enzymatique partiel de la surrénale --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=déficit enzymatique partiel de la surrénale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1342. en:Laron syndrome --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=en:Laron syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1343. en:de Barsy's syndrome --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=en:de Barsy's syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1344. en:developmental anomaly --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=en:developmental anomaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1345. en:hyperlipaemia --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=en:hyperlipaemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1346. en:hyperlipoidaemia --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=en:hyperlipoidaemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1347. en:oligophrenia --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=en:oligophrenia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1348. en:overload disease --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=en:overload disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1349. en:phosphoglycerate kinase 1 deficiency --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=en:phosphoglycerate kinase 1 deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1350. fente labio-palatine --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=fente labio-palatine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1351. fente labiopalatine --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=fente labiopalatine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1352. idiosyncrasie au fructose --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=idiosyncrasie au fructose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1353. mannosidose --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=mannosidose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1354. mucopolysaccharidose de type 1 --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=mucopolysaccharidose de type 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1355. mucopolysaccharidose de type I --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=mucopolysaccharidose de type I | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1356. porphyrinurie --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=porphyrinurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1357. situs inversus viscerum --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=situs inversus viscerum | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1358. syndrome de Prader-Willi --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=syndrome de Prader-Willi | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1359. sécheresse cutanée --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=sécheresse cutanée | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1360. une anomalie congénitale --- r_associated #0: 21 --> en:classical phenylketonuria
    n1=une anomalie congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=21
  1361. Malformation cardiaque --- r_associated #0: 20 --> en:classical phenylketonuria
    n1=Malformation cardiaque | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=20
  1362. déficit en phosphatases alcalines --- r_associated #0: 20 --> en:classical phenylketonuria
    n1=déficit en phosphatases alcalines | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=20
  1363. goût --- r_associated #0: 20 --> en:classical phenylketonuria
    n1=goût | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=20
  1364. ptérygium colli --- r_associated #0: 20 --> en:classical phenylketonuria
    n1=ptérygium colli | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=20
  1365. syndrome de Warburg --- r_associated #0: 16 --> en:classical phenylketonuria
    n1=syndrome de Warburg | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=16
  1366. trisomie 21 --- r_associated #0: 16 --> en:classical phenylketonuria
    n1=trisomie 21 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=16
  1367. Albert (position d') --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Albert (position d') | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1368. Anitschkow (cellule de) --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Anitschkow (cellule de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1369. Arrhenius (loi d') --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Arrhenius (loi d') | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1370. Atrésie --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Atrésie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1371. CARD --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=CARD | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1372. Cystinurie --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Cystinurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1373. Diabète sucré --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Diabète sucré | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1374. Elliott (lambeau d') --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Elliott (lambeau d') | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1375. Fuchs (syndrome de) --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Fuchs (syndrome de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1376. His (faisceau de) --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=His (faisceau de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1377. Hyperplasie congénitale des surrénales --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Hyperplasie congénitale des surrénales | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1378. Intolérance au fructose --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Intolérance au fructose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1379. Maladie de Niemann-Pick --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Maladie de Niemann-Pick | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1380. Maladie génétique --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Maladie génétique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1381. Maladies cardiaques --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Maladies cardiaques | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1382. Malformation congénitale --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Malformation congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1383. Pyurie --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Pyurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1384. Syndrome de Walker-Warburg --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=Syndrome de Walker-Warburg | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1385. atmosphère (composition de l') --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=atmosphère (composition de l') | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1386. cyclope (oeil) --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=cyclope (oeil) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1387. céto-acidose --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=céto-acidose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1388. ectodermitis erosiva pluriorificialis --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=ectodermitis erosiva pluriorificialis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1389. ectodermose --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=ectodermose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1390. ectodermose érosive pluriorificielle de Fiessinger-Rendu --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=ectodermose érosive pluriorificielle de Fiessinger-Rendu | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1391. ectoenzyme --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=ectoenzyme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1392. ectomie --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=ectomie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1393. ectomorphie --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=ectomorphie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1394. ectoparasite --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=ectoparasite | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1395. ectoparasitose --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=ectoparasitose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1396. en:cleft soft palate --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=en:cleft soft palate | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1397. exécutives (fonctions) --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=exécutives (fonctions) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1398. handicap mental --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=handicap mental | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1399. hydrocèle (cure chirurgicale d') --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=hydrocèle (cure chirurgicale d') | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1400. hyperkératose nævoïde (hamartomateuse) du mamelon --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=hyperkératose nævoïde (hamartomateuse) du mamelon | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1401. hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1402. hyperpression fémoropatellaire latérale (syndrome d') --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=hyperpression fémoropatellaire latérale (syndrome d') | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1403. hyperthyroïdie (manifestations neuromusculaires dans l') --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=hyperthyroïdie (manifestations neuromusculaires dans l') | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1404. hypophosphatasie --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=hypophosphatasie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1405. malentendant (enfant) --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=malentendant (enfant) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1406. triple arthrodèse --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=triple arthrodèse | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1407. triple opération à la française --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=triple opération à la française | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1408. triploïdie --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=triploïdie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1409. triptans --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=triptans | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1410. triquétrum --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=triquétrum | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1411. triradialis sulcus de Turner --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=triradialis sulcus de Turner | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1412. tris --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=tris | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1413. trismus --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=trismus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1414. trisomie du bras court du chromosome 3 --- r_associated #0: 15 --> en:classical phenylketonuria
    n1=trisomie du bras court du chromosome 3 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=15
  1415. bilirubinurie --- r_associated #0: 11 --> en:classical phenylketonuria
    n1=bilirubinurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=11
  1416. cystinose --- r_associated #0: 11 --> en:classical phenylketonuria
    n1=cystinose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=11
  1417. mongolisme --- r_associated #0: 11 --> en:classical phenylketonuria
    n1=mongolisme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=11
  1418. troubles de l'anxiété --- r_associated #0: 11 --> en:classical phenylketonuria
    n1=troubles de l'anxiété | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=11
  1419. Acidocétose --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Acidocétose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1420. Acinetobacter --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Acinetobacter | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1421. Albinisme --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Albinisme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1422. Angelman (syndrome d') --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Angelman (syndrome d') | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1423. Anomalie chromosomique --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Anomalie chromosomique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1424. CONGÉNITALE --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=CONGÉNITALE | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1425. Card --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Card | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1426. Cardiopathie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Cardiopathie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1427. Chorée de Huntington --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Chorée de Huntington | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1428. Communication interauriculaire --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Communication interauriculaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1429. Craniosynostose --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Craniosynostose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1430. Cétoacidose --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Cétoacidose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1431. Dubin-Johnson (syndrome de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Dubin-Johnson (syndrome de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1432. Déficience mentale --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Déficience mentale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1433. Ectoparasite --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Ectoparasite | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1434. Fucosidose --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Fucosidose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1435. Glycogénose --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Glycogénose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1436. Goutte
    (maladie)
     --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Goutte
    (maladie)
    | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1437. Haltia-Santavuori (maladie de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Haltia-Santavuori (maladie de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1438. Hernie ombilicale --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Hernie ombilicale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1439. Histidinémie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Histidinémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1440. Hydrocéphalie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Hydrocéphalie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1441. Hyperlipidémie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Hyperlipidémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1442. Hyperlipémie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Hyperlipémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1443. Hyperthermie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Hyperthermie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1444. Hypertélorisme --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Hypertélorisme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1445. Hypoplasie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Hypoplasie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1446. Jumeaux siamois --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Jumeaux siamois | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1447. Laparoschisis --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Laparoschisis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1448. Laurence-Moon (syndrome de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Laurence-Moon (syndrome de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1449. Lowe (syndrome de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Lowe (syndrome de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1450. Macroglossie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Macroglossie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1451. Malformation --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Malformation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1452. Manning (score de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Manning (score de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1453. Mannosidose --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Mannosidose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1454. Marchiafava-Micheli (maladie de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Marchiafava-Micheli (maladie de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1455. Martin-Bell (syndrome de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Martin-Bell (syndrome de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1456. Michon (opération de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Michon (opération de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1457. Microalbuminurie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Microalbuminurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1458. Niemann-Pick (maladie de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Niemann-Pick (maladie de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1459. Phénylcétonurie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Phénylcétonurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1460. Polyurie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Polyurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1461. Progéria --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Progéria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1462. Roger (maladie de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Roger (maladie de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1463. Sipple (syndrome de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Sipple (syndrome de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1464. Situs inversus --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Situs inversus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1465. Sydenham (chorée de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Sydenham (chorée de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1466. Syndrome de De Barsy --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Syndrome de De Barsy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1467. Syndrome de Lowe --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Syndrome de Lowe | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1468. Syndrome de Prader-Willi --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Syndrome de Prader-Willi | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1469. Trisomie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Trisomie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1470. Völker-Dieben (atrophie optique liée au sexe de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Völker-Dieben (atrophie optique liée au sexe de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1471. Went (atrophie optique liée au sexe de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=Went (atrophie optique liée au sexe de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1472. aberration chromosomique --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=aberration chromosomique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1473. acidurie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=acidurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1474. acidurie 3-hydroxy-3-méthyl-glutarique --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=acidurie 3-hydroxy-3-méthyl-glutarique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1475. acidurie 3-méthylglutaconique --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=acidurie 3-méthylglutaconique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1476. acidurie 4-hydroxybutyrique --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=acidurie 4-hydroxybutyrique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1477. acidurie paradoxale --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=acidurie paradoxale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1478. acineux --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=acineux | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1479. acini --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=acini | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1480. acinus --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=acinus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1481. acinus hépatique de Rappaport --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=acinus hépatique de Rappaport | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1482. alcalose métabolique (classification) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=alcalose métabolique (classification) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1483. bec de corbin --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=bec de corbin | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1484. bec de cuiller --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=bec de cuiller | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1485. bec de la prostate --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=bec de la prostate | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1486. bec de la rotule --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=bec de la rotule | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1487. bébé collodion --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=bébé collodion | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1488. chorde --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=chorde | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1489. chorde dorsale --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=chorde dorsale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1490. chordome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=chordome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1491. chordomésoblaste --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=chordomésoblaste | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1492. chorio-amniotite --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=chorio-amniotite | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1493. chorio-angiome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=chorio-angiome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1494. chorio-épithéliome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=chorio-épithéliome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1495. choriocapillaire --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=choriocapillaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1496. choriocarcinome germinal tératomateux du médiastin --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=choriocarcinome germinal tératomateux du médiastin | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1497. choriocarcinome placentaire --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=choriocarcinome placentaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1498. choriocarcinome primitif du col utérin --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=choriocarcinome primitif du col utérin | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1499. choriogonadotrophine --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=choriogonadotrophine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1500. chorioméningite lymphocytaire --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=chorioméningite lymphocytaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1501. cornée et tyrosinose de type II --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=cornée et tyrosinose de type II | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1502. coup de chaleur --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=coup de chaleur | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1503. cystinique (lithiase) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=cystinique (lithiase) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1504. danse de Saint Guy --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=danse de Saint Guy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1505. de Barsy (syndrome de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=de Barsy (syndrome de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1506. de type I --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=de type I | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1507. diabète non-insulinodépendant --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=diabète non-insulinodépendant | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1508. diabète phosphaté --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=diabète phosphaté | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1509. diabète post-transplantation --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=diabète post-transplantation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1510. diabète rénal --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=diabète rénal | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1511. déficit intellectuel --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=déficit intellectuel | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1512. ectopie des procès ciliaires --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=ectopie des procès ciliaires | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1513. ectopie du cristallin --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=ectopie du cristallin | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1514. en:5p minus syndrome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:5p minus syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1515. en:Albert's position --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Albert's position | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1516. en:Anitschkow's cell --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Anitschkow's cell | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1517. en:Arrhenius'law --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Arrhenius'law | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1518. en:Chopart's amputation --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Chopart's amputation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1519. en:Down's --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Down's | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1520. en:Down's syndrome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Down's syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1521. en:Elliott lateral flap --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Elliott lateral flap | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1522. en:Fenn's diagram --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Fenn's diagram | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1523. en:HHH syndrome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:HHH syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1524. en:Huntington's chorea --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Huntington's chorea | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1525. en:Lejeune's syndrome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Lejeune's syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1526. en:Lowe's disease --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Lowe's disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1527. en:PWS --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:PWS | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1528. en:Siamese twin brothers --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Siamese twin brothers | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1529. en:Smith-Magenis syndrome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Smith-Magenis syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1530. en:Tay Sachs' disease --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Tay Sachs' disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1531. en:WBS --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:WBS | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1532. en:Williams' syndrome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Williams' syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1533. en:Williams-Beuren syndrome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:Williams-Beuren syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1534. en:alcaptonuria --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:alcaptonuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1535. en:and cerebral dysfonction --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:and cerebral dysfonction | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1536. en:and growth retardation --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:and growth retardation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1537. en:and postaxil polydactylie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:and postaxil polydactylie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1538. en:and sensorineural deafness --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:and sensorineural deafness | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1539. en:atresia ani --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:atresia ani | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1540. en:bloody urine --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:bloody urine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1541. en:bronze baby syndrome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:bronze baby syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1542. en:cacomorphosis --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:cacomorphosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1543. en:cat cry disease --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:cat cry disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1544. en:cat cry syndrome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:cat cry syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1545. en:chromosomal disorder --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:chromosomal disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1546. en:chromosome 5p deletion syndrome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:chromosome 5p deletion syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1547. en:conjoined twin brothers --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:conjoined twin brothers | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1548. en:conjoints twins --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:conjoints twins | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1549. en:contractural arachnodactyly --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:contractural arachnodactyly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1550. en:coronary disease --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:coronary disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1551. en:cyclops eye --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:cyclops eye | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1552. en:de Barsy?s syndrome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:de Barsy?s syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1553. en:de Sanctis-Cacchione syndrome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:de Sanctis-Cacchione syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1554. en:diabetic strokes --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:diabetic strokes | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1555. en:dyslipaemia --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:dyslipaemia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1556. en:ectodermosis --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:ectodermosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1557. en:ectodermosis erosiva pluriorificialis --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:ectodermosis erosiva pluriorificialis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1558. en:ectoenzyme --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:ectoenzyme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1559. en:ectoparasite --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:ectoparasite | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1560. en:ectoparasitosis --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:ectoparasitosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1561. en:ectrodactyly and macular dystrophy --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:ectrodactyly and macular dystrophy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1562. en:endocrine disorder --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:endocrine disorder | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1563. en:executive functions --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:executive functions | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1564. en:eye abnormality --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:eye abnormality | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1565. en:facial clefting syndrome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:facial clefting syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1566. en:glycogenosis --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:glycogenosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1567. en:gross hematuria --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:gross hematuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1568. en:heart condition --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:heart condition | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1569. en:homogentisuria --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:homogentisuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1570. en:hyperkeratosis of nipple and areola --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:hyperkeratosis of nipple and areola | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1571. en:hyperornithinemia hyperammoniemia homocitrullinuria --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:hyperornithinemia hyperammoniemia homocitrullinuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1572. en:hyperprolinemia. --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:hyperprolinemia. | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1573. en:hypoacousic child --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:hypoacousic child | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1574. en:hypospadias --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:hypospadias | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1575. en:infantile finnish type --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:infantile finnish type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1576. en:interatrial septal defect --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:interatrial septal defect | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1577. en:interventricular septal defect --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:interventricular septal defect | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1578. en:iris coloboma with ptosis --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:iris coloboma with ptosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1579. en:labiopalatine cleft --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:labiopalatine cleft | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1580. en:microtia --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:microtia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1581. en:minimal pigment type --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:minimal pigment type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1582. en:multicore disease with mental retardation --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:multicore disease with mental retardation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1583. en:myopia --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:myopia | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1584. en:nephropathy --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:nephropathy | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1585. en:phosphatide thesaurismosis --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:phosphatide thesaurismosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1586. en:polysyndactyly syndrome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:polysyndactyly syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1587. en:porphyuria --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:porphyuria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1588. en:secundum defect --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:secundum defect | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1589. en:sinus venosus defect --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:sinus venosus defect | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1590. en:surgical treatment of hydrocele --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:surgical treatment of hydrocele | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1591. en:trisomy 21 --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:trisomy 21 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1592. en:type II --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:type II | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1593. en:unusual facies --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:unusual facies | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1594. en:uroporphyria --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:uroporphyria | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1595. en:water on the brain --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:water on the brain | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1596. en:with deafness --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:with deafness | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1597. en:xanthine lithiasis --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=en:xanthine lithiasis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1598. faciale (paralysie du nouveau-né) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=faciale (paralysie du nouveau-né) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1599. fente cérébrale de Bichat --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=fente cérébrale de Bichat | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1600. fente de Larrey --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=fente de Larrey | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1601. fente de la glotte --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=fente de la glotte | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1602. fente du voile du palais --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=fente du voile du palais | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1603. fente foetale --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=fente foetale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1604. fente hypophysaire --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=fente hypophysaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1605. fente interaryténoïdienne --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=fente interaryténoïdienne | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1606. fente interfessière --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=fente interfessière | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1607. fente labiopalatine et kystes muqueux de la lèvre inférieure --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=fente labiopalatine et kystes muqueux de la lèvre inférieure | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1608. fente labiopalatine, ectropion et dents coniques --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=fente labiopalatine, ectropion et dents coniques | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1609. fente labiopalatine, kyste paramédian muqueux de la lèvre inférieure, ptérygium poplité et anomalies digitogénitales --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=fente labiopalatine, kyste paramédian muqueux de la lèvre inférieure, ptérygium poplité et anomalies digitogénitales | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1610. fente nasolabiopalatine --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=fente nasolabiopalatine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1611. fénotérol --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=fénotérol | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1612. glycogénique (surcharge et infiltration) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=glycogénique (surcharge et infiltration) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1613. goniome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=goniome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1614. goniomètre --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=goniomètre | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1615. gonion --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=gonion | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1616. gonioscopie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=gonioscopie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1617. goniosynéchies --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=goniosynéchies | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1618. goniotomie endoscopique --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=goniotomie endoscopique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1619. gonochorisme --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=gonochorisme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1620. gonococcie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=gonococcie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1621. gonocoque --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=gonocoque | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1622. gonocyte --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=gonocyte | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1623. gonocytome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=gonocytome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1624. gonométrie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=gonométrie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1625. gonorrhée --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=gonorrhée | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1626. gonosome --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=gonosome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1627. gonosomique --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=gonosomique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1628. hernie diaphragmatique --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hernie diaphragmatique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1629. hydrocephalus --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hydrocephalus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1630. hyperlipoprotéinémie de type I --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hyperlipoprotéinémie de type I | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1631. hyperphorie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hyperphorie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1632. hyperphorie alternante --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hyperphorie alternante | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1633. hyperphosphatasie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hyperphosphatasie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1634. hyperphosphatasémie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hyperphosphatasémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1635. hyperphosphatasémie chronique congénitale idiopathique --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hyperphosphatasémie chronique congénitale idiopathique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1636. hyperphosphatémie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hyperphosphatémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1637. hypertensinase --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hypertensinase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1638. hypertensine --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hypertensine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1639. hypertensinogène --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hypertensinogène | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1640. hypertension --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hypertension | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1641. hypertension abdominale --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hypertension abdominale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1642. hypertension artérielle --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hypertension artérielle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1643. hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1644. hypohypophysie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hypohypophysie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1645. hypophosphatasies --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hypophosphatasies | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1646. hypostimulinie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hypostimulinie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1647. hémochromatose génétique (mutations responsables de l') --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=hémochromatose génétique (mutations responsables de l') | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1648. impédance acoustique (symb. Z) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=impédance acoustique (symb. Z) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1649. maladie de niemann-pick --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=maladie de niemann-pick | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1650. nanisme --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=nanisme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1651. nanisme de type Laron --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=nanisme de type Laron | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1652. neuraminidase (déficit en) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=neuraminidase (déficit en) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1653. neurofibromatose de type périphérique --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=neurofibromatose de type périphérique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1654. nystagmus --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=nystagmus | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1655. nystagmus héréditaire vertical --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=nystagmus héréditaire vertical | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1656. nystagmus lié au sexe --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=nystagmus lié au sexe | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1657. nystagmus myoclonies --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=nystagmus myoclonies | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1658. omovertébral (os) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=omovertébral (os) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1659. peau ridée (syndrome de la) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=peau ridée (syndrome de la) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1660. porphyries (neuropathies des) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=porphyries (neuropathies des) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1661. profondeur de l'anesthésie (stade de) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=profondeur de l'anesthésie (stade de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1662. prolidase (déficit en) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=prolidase (déficit en) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1663. ptérygions (syndrome des) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=ptérygions (syndrome des) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1664. quadriplégie spastique, rétinite pigmentaire et retard mental --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=quadriplégie spastique, rétinite pigmentaire et retard mental | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1665. retard mental avec atrophie optique, surdité et épilepsie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=retard mental avec atrophie optique, surdité et épilepsie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1666. rétention hydrochlorurée sodique --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=rétention hydrochlorurée sodique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1667. rétention membraneuse --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=rétention membraneuse | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1668. rétention placentaire --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=rétention placentaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1669. rétention placentaire du postabortum --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=rétention placentaire du postabortum | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1670. rétention sudorale --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=rétention sudorale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1671. rétentionniste --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=rétentionniste | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1672. rétinite pigmentaire et retard mental --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=rétinite pigmentaire et retard mental | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1673. rétinite pigmentaire, surdité, retard mental, et hypogonadisme --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=rétinite pigmentaire, surdité, retard mental, et hypogonadisme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1674. sirtuine --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=sirtuine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1675. sisi-test --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=sisi-test | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1676. sismothérapie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=sismothérapie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1677. surdité --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=surdité | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1678. syndrome cataracte-ataxie-surdité et retard mental --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=syndrome cataracte-ataxie-surdité et retard mental | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1679. syndrome de Nathalie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=syndrome de Nathalie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1680. syndrome de Rathbun --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=syndrome de Rathbun | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1681. syndrome de Treft-Sanborn-Carey --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=syndrome de Treft-Sanborn-Carey | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1682. syndrome de warburg --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=syndrome de warburg | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1683. syndrome de zellweger --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=syndrome de zellweger | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1684. sècheresse cutanée --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=sècheresse cutanée | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1685. trichomégalie avec retard mental, nanisme, et dégénérescence pigmentée de la rétine --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=trichomégalie avec retard mental, nanisme, et dégénérescence pigmentée de la rétine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1686. triphosphopyridine-nucléotide --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=triphosphopyridine-nucléotide | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1687. trisomie 9p --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=trisomie 9p | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1688. télécardiographie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=télécardiographie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1689. télécardiophone --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=télécardiophone | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1690. téléclitoridie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=téléclitoridie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1691. télécobalt --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=télécobalt | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1692. télécobalt-thérapie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=télécobalt-thérapie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1693. téléconsultation --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=téléconsultation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1694. télécrâne --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=télécrâne | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1695. télécæsiothérapie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=télécæsiothérapie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1696. télédermatologie --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=télédermatologie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1697. télédiastole --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=télédiastole | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1698. télédétection --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=télédétection | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1699. urticaire-surdité-amylose rénale --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=urticaire-surdité-amylose rénale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1700. uréosecrétoire (constante) --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=uréosecrétoire (constante) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1701. xanthomatose familiale primitive --- r_associated #0: 10 --> en:classical phenylketonuria
    n1=xanthomatose familiale primitive | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=10
  1702. acidurie hydroxyméthylglutarique --- r_associated #0: 6 --> en:classical phenylketonuria
    n1=acidurie hydroxyméthylglutarique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=6
  1703. choréo-acanthocytose --- r_associated #0: 6 --> en:classical phenylketonuria
    n1=choréo-acanthocytose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=6
  1704. trisomie 18 --- r_associated #0: 6 --> en:classical phenylketonuria
    n1=trisomie 18 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=6
  1705. ANKRD11 gene --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=ANKRD11 gene | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1706. ARRX --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=ARRX | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1707. Exomphale --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=Exomphale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1708. Fente labiale --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=Fente labiale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1709. Fente palatine --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=Fente palatine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1710. Gaucher (maladie de) --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=Gaucher (maladie de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1711. Gusberg et Kaplan (classification de) --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=Gusberg et Kaplan (classification de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1712. Handicap mental --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=Handicap mental | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1713. Hypopituitarisme --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=Hypopituitarisme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1714. Hématurie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=Hématurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1715. Maladie du cri du chat --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=Maladie du cri du chat | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1716. Ptérygium colli --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=Ptérygium colli | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1717. Tay-Sachs (maladie de) --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=Tay-Sachs (maladie de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1718. Williams (syndrome de) --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=Williams (syndrome de) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1719. acidurie isovalérique --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=acidurie isovalérique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1720. acidurie méthylmalonique avec homocystinurie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=acidurie méthylmalonique avec homocystinurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1721. albinisme avec immunodéficience et troubles hématologiques --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=albinisme avec immunodéficience et troubles hématologiques | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1722. albinisme avec surdité --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=albinisme avec surdité | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1723. ankyloblépharon --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=ankyloblépharon | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1724. ankyloblépharon filiforme et fente palatine --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=ankyloblépharon filiforme et fente palatine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1725. ankyloblépharon, ongles hypoplasiques et cheveux bouclés --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=ankyloblépharon, ongles hypoplasiques et cheveux bouclés | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1726. ankyloblépharon-dysplasie ectodermique-fente labio-palatine --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=ankyloblépharon-dysplasie ectodermique-fente labio-palatine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1727. arrière-pied --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=arrière-pied | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1728. bec de perroquet --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=bec de perroquet | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1729. bec du cuboïde --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=bec du cuboïde | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1730. bec du sphénoïde --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=bec du sphénoïde | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1731. bec scléral --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=bec scléral | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1732. bec-de-lièvre non précisé --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=bec-de-lièvre non précisé | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1733. bécégite --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=bécégite | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1734. chorial, ale --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=chorial, ale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1735. chorio-adénome destruens --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=chorio-adénome destruens | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1736. chorée fibrillaire de Morvan --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=chorée fibrillaire de Morvan | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1737. chorée gravidique --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=chorée gravidique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1738. cri du chat (maladie du) --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=cri du chat (maladie du) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1739. cyclopeptide --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=cyclopeptide | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1740. cyclophiline --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=cyclophiline | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1741. cyclophorie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=cyclophorie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1742. cyclophosphamide --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=cyclophosphamide | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1743. cyclophotocoagulation endoscopique --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=cyclophotocoagulation endoscopique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1744. cyclophrénie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=cyclophrénie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1745. cyclophyllidés --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=cyclophyllidés | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1746. diabète bronzé --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabète bronzé | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1747. diabète de type 1 --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabète de type 1 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1748. diabète de type 2 --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabète de type 2 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1749. diabète et psychisme --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabète et psychisme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1750. diabète et surdité d'origine mitochondriale --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabète et surdité d'origine mitochondriale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1751. diabète gestationnel --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabète gestationnel | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1752. diabète gras --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabète gras | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1753. diabète insipide --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabète insipide | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1754. diabète insipide néphrogénique --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabète insipide néphrogénique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1755. diabète insulino-requérant --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabète insulino-requérant | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1756. diabète insulinodépendant --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabète insulinodépendant | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1757. diabète lipoatrophique congénital --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabète lipoatrophique congénital | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1758. diabète sucré et complications rénales --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabète sucré et complications rénales | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1759. diabètes monogéniques --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabètes monogéniques | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1760. diabètes sucrés et insipides avec atrophie optique et surdité --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabètes sucrés et insipides avec atrophie optique et surdité | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1761. diabétide génitale --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=diabétide génitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1762. ellipse d'engagement --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=ellipse d'engagement | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1763. ellipt.ocytose --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=ellipt.ocytose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1764. elliptocyte --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=elliptocyte | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1765. elliptocytose --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=elliptocytose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1766. en:Sachs' disease --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=en:Sachs' disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1767. en:cat's cry syndrome --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=en:cat's cry syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1768. en:club-footed person --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=en:club-footed person | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1769. en:person with a club foot --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=en:person with a club foot | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1770. en:person with a clubfoot --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=en:person with a clubfoot | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1771. exencéphale --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=exencéphale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1772. exénatide --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=exénatide | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1773. faisceau de His --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=faisceau de His | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1774. fuchsine --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=fuchsine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1775. fucose --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=fucose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1776. fucosidase --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=fucosidase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1777. fucoside --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=fucoside | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1778. histaminergie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=histaminergie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1779. histaminergique --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=histaminergique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1780. histaminique --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=histaminique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1781. histaminolibération --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=histaminolibération | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1782. histaminolytique --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=histaminolytique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1783. histaminopexie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=histaminopexie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1784. histaminurie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=histaminurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1785. histaminémie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=histaminémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1786. histidase --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=histidase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1787. histidinase --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=histidinase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1788. histidine --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=histidine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1789. histidine-ammoniac-lyase --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=histidine-ammoniac-lyase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1790. histidine-décarboxylase --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=histidine-décarboxylase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1791. histidine-désaminase --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=histidine-désaminase | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1792. hydrocèle de la femme --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hydrocèle de la femme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1793. hydrocèle de la vaginale --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hydrocèle de la vaginale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1794. hydrocèle du canal de Nück --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hydrocèle du canal de Nück | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1795. hydrocèle du cou --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hydrocèle du cou | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1796. hyperkeratosis follicularis et parafollicularis in cutem penetrans de Kyrle --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperkeratosis follicularis et parafollicularis in cutem penetrans de Kyrle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1797. hyperkeratosis lenticularis perstans de Flegel --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperkeratosis lenticularis perstans de Flegel | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1798. hyperkinésie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperkinésie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1799. hyperkinésie volitionnelle --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperkinésie volitionnelle | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1800. hyperlacrymie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperlacrymie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1801. hyperlactacidémie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperlactacidémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1802. hyperlaxité articulaire familiale --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperlaxité articulaire familiale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1803. hyperlaxité ligamentaire --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperlaxité ligamentaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1804. hyperleucocytose --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperleucocytose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1805. hyperostose vertébrale ankylosante --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperostose vertébrale ankylosante | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1806. hyperoxalurie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperoxalurie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1807. hyperoxalémie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperoxalémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1808. hyperphagie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperphagie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1809. hyperphalangie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperphalangie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1810. hyperphosphorémie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperphosphorémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1811. hyperpigmentation --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperpigmentation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1812. hyperpigmentation familiale des paupières --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperpigmentation familiale des paupières | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1813. hyperpigmentation familiale progressive --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperpigmentation familiale progressive | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1814. hyperpigmentation flagellée --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperpigmentation flagellée | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1815. hyperpigmentation médicamenteuse --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperpigmentation médicamenteuse | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1816. hyperpigmentation palmoplantaire physiologique --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperpigmentation palmoplantaire physiologique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1817. hyperpipécolatémie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperpipécolatémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1818. hyperplaquettose --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperplaquettose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1819. hyperplasie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperplasie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1820. hyperplasie adénomateuse de l'endomètre --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperplasie adénomateuse de l'endomètre | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1821. hyperplasie adénomateuse isolée du sein --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperplasie adénomateuse isolée du sein | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1822. hyperplasie angiolymphoïde avec éosinophilie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperplasie angiolymphoïde avec éosinophilie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1823. hyperprolactinémie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperprolactinémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1824. hyperprothrombinémie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperprothrombinémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1825. hyperprotidémie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperprotidémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1826. hyperprotéinorachie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperprotéinorachie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1827. hyperprotéinémie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperprotéinémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1828. hyperptyalisme --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperptyalisme | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1829. hyperpyruvicémie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hyperpyruvicémie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1830. hypertrichose congénitale des cils --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hypertrichose congénitale des cils | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1831. hypertrichose lanugineuse acquise --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hypertrichose lanugineuse acquise | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1832. hypertrichose lanugineuse congénitale --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hypertrichose lanugineuse congénitale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1833. hypertrichose nævoïde --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hypertrichose nævoïde | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1834. hypertrichose-atrophie cutanée-ectropion et macrostomie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hypertrichose-atrophie cutanée-ectropion et macrostomie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1835. hypertrichosis universalis congenita --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=hypertrichosis universalis congenita | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1836. malf ormation dysraphique --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=malf ormation dysraphique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1837. malformation kystique adénomatoïde du poumon --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=malformation kystique adénomatoïde du poumon | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1838. malformation luxante de la hanche --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=malformation luxante de la hanche | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1839. malformation mamelonnaire --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=malformation mamelonnaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1840. malformation mammaire --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=malformation mammaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1841. malformation ombilicale --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=malformation ombilicale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1842. malformation utérine --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=malformation utérine | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1843. malformation vaginale --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=malformation vaginale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1844. malformation vasculaire cérébrale du nourrisson --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=malformation vasculaire cérébrale du nourrisson | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1845. malformations de la charnière occipitocervicale --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=malformations de la charnière occipitocervicale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1846. neurinome bilatéral du nerf cochléaire (VIII) --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=neurinome bilatéral du nerf cochléaire (VIII) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1847. nystagmus (zone de moindre) --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=nystagmus (zone de moindre) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1848. parfait (stade) --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=parfait (stade) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1849. semidominance --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=semidominance | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1850. semiquinone --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=semiquinone | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1851. syndrome d'hyperperméabilité capillaire --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=syndrome d'hyperperméabilité capillaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1852. syndrome d'hyperpression fémoropatellaire latérale --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=syndrome d'hyperpression fémoropatellaire latérale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1853. syndrome de Fuchs --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=syndrome de Fuchs | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1854. syndrome tumeur de Wilms-aniridie-anomalies génito-urinaires-retard mental --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=syndrome tumeur de Wilms-aniridie-anomalies génito-urinaires-retard mental | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1855. séminal --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=séminal | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1856. séminifère --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=séminifère | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1857. séminomateux --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=séminomateux | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1858. séminome --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=séminome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1859. séminome de l'ovaire --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=séminome de l'ovaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1860. séminome du médiastin --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=séminome du médiastin | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1861. séminome spermatocytaire --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=séminome spermatocytaire | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1862. sémiochimique --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=sémiochimique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1863. sémiologie extrapyramidale --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=sémiologie extrapyramidale | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1864. triplet (CGG) n --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=triplet (CGG) n | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1865. trisomie 13 --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=trisomie 13 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1866. trisomie 17p11.2 --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=trisomie 17p11.2 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1867. trisomie 8 --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=trisomie 8 | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1868. xanthoastrocytome pléomorphe --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=xanthoastrocytome pléomorphe | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1869. xanthochromie --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=xanthochromie | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1870. xanthochromie caroténique --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=xanthochromie caroténique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1871. xanthoerythrodermia perstans --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=xanthoerythrodermia perstans | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1872. xanthogranulome juvénile --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=xanthogranulome juvénile | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1873. xanthogranulome nécrobiotique --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=xanthogranulome nécrobiotique | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1874. xanthogranulome palpébral --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=xanthogranulome palpébral | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1875. xanthohistiocytome --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=xanthohistiocytome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1876. xanthoma disseminatum --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=xanthoma disseminatum | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1877. xanthomatose --- r_associated #0: 5 --> en:classical phenylketonuria
    n1=xanthomatose | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=5
  1878. en:taste perception --- r_associated #0: -120 --> en:classical phenylketonuria
    n1=en:taste perception | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=-120
  1879. gustation --- r_associated #0: -120 --> en:classical phenylketonuria
    n1=gustation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=-120
  1880. en:gustation --- r_associated #0: -125 --> en:classical phenylketonuria
    n1=en:gustation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=-125
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