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'en:leucinosis'
(id=16848501 ; fe=en:leucinosis ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=31793 creation date=2021-07-25 touchdate=2026-01-08 15:29:43.000)
≈ 1341 relations sortantes

  1. en:leucinosis -- r_associated #0: 52 / 1 -> en:glutathione s-transferase deficiency
    n1=en:leucinosis | n2=en:glutathione s-transferase deficiency | rel=r_associated | relid=0 | w=52
  2. en:leucinosis -- r_associated #0: 52 / 1 -> en:hemophagocytic lymphohistiocytosis
    n1=en:leucinosis | n2=en:hemophagocytic lymphohistiocytosis | rel=r_associated | relid=0 | w=52
  3. en:leucinosis -- r_associated #0: 52 / 1 -> en:maple syrup urine disease, type ii
    n1=en:leucinosis | n2=en:maple syrup urine disease, type ii | rel=r_associated | relid=0 | w=52
  4. en:leucinosis -- r_associated #0: 52 / 1 -> en:other disorders of branched-chain amino-acid metabolism
    n1=en:leucinosis | n2=en:other disorders of branched-chain amino-acid metabolism | rel=r_associated | relid=0 | w=52
  5. en:leucinosis -- r_associated #0: 51 / 0.981 -> en:ectrodactyly
    n1=en:leucinosis | n2=en:ectrodactyly | rel=r_associated | relid=0 | w=51
  6. en:leucinosis -- r_associated #0: 50 / 0.962 -> en:gray platelet syndrome
    n1=en:leucinosis | n2=en:gray platelet syndrome | rel=r_associated | relid=0 | w=50
  7. en:leucinosis -- r_associated #0: 50 / 0.962 -> en:rehabilitation aspects
    n1=en:leucinosis | n2=en:rehabilitation aspects | rel=r_associated | relid=0 | w=50
  8. en:leucinosis -- r_associated #0: 49 / 0.942 -> en:fatal familial insomnia
    n1=en:leucinosis | n2=en:fatal familial insomnia | rel=r_associated | relid=0 | w=49
  9. en:leucinosis -- r_associated #0: 48 / 0.923 -> en:papillon-lefevre syndrome
    n1=en:leucinosis | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=48
  10. en:leucinosis -- r_associated #0: 48 / 0.923 -> en:sweet syndrome
    n1=en:leucinosis | n2=en:sweet syndrome | rel=r_associated | relid=0 | w=48
  11. en:leucinosis -- r_associated #0: 47 / 0.904 -> en:perthes disease
    n1=en:leucinosis | n2=en:perthes disease | rel=r_associated | relid=0 | w=47
  12. en:leucinosis -- r_associated #0: 46 / 0.885 -> en:giant axonal neuropathy
    n1=en:leucinosis | n2=en:giant axonal neuropathy | rel=r_associated | relid=0 | w=46
  13. en:leucinosis -- r_associated #0: 46 / 0.885 -> en:mansonelliasis
    n1=en:leucinosis | n2=en:mansonelliasis | rel=r_associated | relid=0 | w=46
  14. en:leucinosis -- r_associated #0: 46 / 0.885 -> en:myhre syndrome
    n1=en:leucinosis | n2=en:myhre syndrome | rel=r_associated | relid=0 | w=46
  15. en:leucinosis -- r_associated #0: 45 / 0.865 -> en:behr syndrome
    n1=en:leucinosis | n2=en:behr syndrome | rel=r_associated | relid=0 | w=45
  16. en:leucinosis -- r_associated #0: 45 / 0.865 -> en:berardinelli-seip congenital lipodystrophy
    n1=en:leucinosis | n2=en:berardinelli-seip congenital lipodystrophy | rel=r_associated | relid=0 | w=45
  17. en:leucinosis -- r_associated #0: 45 / 0.865 -> en:nutritional management
    n1=en:leucinosis | n2=en:nutritional management | rel=r_associated | relid=0 | w=45
  18. en:leucinosis -- r_associated #0: 45 / 0.865 -> en:ossification of posterior longitudinal ligament
    n1=en:leucinosis | n2=en:ossification of posterior longitudinal ligament | rel=r_associated | relid=0 | w=45
  19. en:leucinosis -- r_associated #0: 44 / 0.846 -> en:argininemia
    n1=en:leucinosis | n2=en:argininemia | rel=r_associated | relid=0 | w=44
  20. en:leucinosis -- r_associated #0: 44 / 0.846 -> en:fryns syndrome
    n1=en:leucinosis | n2=en:fryns syndrome | rel=r_associated | relid=0 | w=44
  21. en:leucinosis -- r_associated #0: 44 / 0.846 -> en:hypophosphatemic rickets with hypercalciuria, hereditary
    n1=en:leucinosis | n2=en:hypophosphatemic rickets with hypercalciuria, hereditary | rel=r_associated | relid=0 | w=44
  22. en:leucinosis -- r_associated #0: 44 / 0.846 -> en:lethargy
    n1=en:leucinosis | n2=en:lethargy | rel=r_associated | relid=0 | w=44
  23. en:leucinosis -- r_associated #0: 44 / 0.846 -> en:li-fraumeni syndrome
    n1=en:leucinosis | n2=en:li-fraumeni syndrome | rel=r_associated | relid=0 | w=44
  24. en:leucinosis -- r_associated #0: 44 / 0.846 -> en:metabolic aspects
    n1=en:leucinosis | n2=en:metabolic aspects | rel=r_associated | relid=0 | w=44
  25. en:leucinosis -- r_associated #0: 44 / 0.846 -> en:mixed connective tissue disease
    n1=en:leucinosis | n2=en:mixed connective tissue disease | rel=r_associated | relid=0 | w=44
  26. en:leucinosis -- r_associated #0: 44 / 0.846 -> en:moderate steroid 21-hydroxylase deficiency
    n1=en:leucinosis | n2=en:moderate steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=44
  27. en:leucinosis -- r_associated #0: 44 / 0.846 -> en:multiple system atrophy
    n1=en:leucinosis | n2=en:multiple system atrophy | rel=r_associated | relid=0 | w=44
  28. en:leucinosis -- r_associated #0: 44 / 0.846 -> en:nephrocalcinosis
    n1=en:leucinosis | n2=en:nephrocalcinosis | rel=r_associated | relid=0 | w=44
  29. en:leucinosis -- r_associated #0: 44 / 0.846 -> en:swyer james syndrome
    n1=en:leucinosis | n2=en:swyer james syndrome | rel=r_associated | relid=0 | w=44
  30. en:leucinosis -- r_associated #0: 44 / 0.846 -> maladie
    (végétaux)
    n1=en:leucinosis | n2=maladie
    (végétaux)
    | rel=r_associated | relid=0 | w=44
  31. en:leucinosis -- r_associated #0: 42 / 0.808 -> complexe 3-méthyl-2-oxobutanoate déshydrogénase
    n1=en:leucinosis | n2=complexe 3-méthyl-2-oxobutanoate déshydrogénase | rel=r_associated | relid=0 | w=42
  32. en:leucinosis -- r_associated #0: 42 / 0.808 -> en:behrens baumann dust syndrome
    n1=en:leucinosis | n2=en:behrens baumann dust syndrome | rel=r_associated | relid=0 | w=42
  33. en:leucinosis -- r_associated #0: 42 / 0.808 -> en:connexin 26 gene anomaly
    n1=en:leucinosis | n2=en:connexin 26 gene anomaly | rel=r_associated | relid=0 | w=42
  34. en:leucinosis -- r_associated #0: 42 / 0.808 -> en:five clinical variants of msud unassociated with genotype
    n1=en:leucinosis | n2=en:five clinical variants of msud unassociated with genotype | rel=r_associated | relid=0 | w=42
  35. en:leucinosis -- r_associated #0: 42 / 0.808 -> en:hereditary elliptocytosis
    n1=en:leucinosis | n2=en:hereditary elliptocytosis | rel=r_associated | relid=0 | w=42
  36. en:leucinosis -- r_associated #0: 42 / 0.808 -> en:homocarnosinosis
    n1=en:leucinosis | n2=en:homocarnosinosis | rel=r_associated | relid=0 | w=42
  37. en:leucinosis -- r_associated #0: 42 / 0.808 -> en:masa syndrome (disorder)
    n1=en:leucinosis | n2=en:masa syndrome (disorder) | rel=r_associated | relid=0 | w=42
  38. en:leucinosis -- r_associated #0: 42 / 0.808 -> en:ochronosis
    n1=en:leucinosis | n2=en:ochronosis | rel=r_associated | relid=0 | w=42
  39. en:leucinosis -- r_associated #0: 41 / 0.788 -> en:bartter syndrome
    n1=en:leucinosis | n2=en:bartter syndrome | rel=r_associated | relid=0 | w=41
  40. en:leucinosis -- r_associated #0: 41 / 0.788 -> en:diagnosis aspect
    n1=en:leucinosis | n2=en:diagnosis aspect | rel=r_associated | relid=0 | w=41
  41. en:leucinosis -- r_associated #0: 41 / 0.788 -> en:dyskeratosis congenita
    n1=en:leucinosis | n2=en:dyskeratosis congenita | rel=r_associated | relid=0 | w=41
  42. en:leucinosis -- r_associated #0: 41 / 0.788 -> en:high molecular weight kininogen deficiency
    n1=en:leucinosis | n2=en:high molecular weight kininogen deficiency | rel=r_associated | relid=0 | w=41
  43. en:leucinosis -- r_associated #0: 41 / 0.788 -> en:hyperlipoproteinemia type i
    n1=en:leucinosis | n2=en:hyperlipoproteinemia type i | rel=r_associated | relid=0 | w=41
  44. en:leucinosis -- r_associated #0: 41 / 0.788 -> en:inherited disorder of bilirubin metabolism
    n1=en:leucinosis | n2=en:inherited disorder of bilirubin metabolism | rel=r_associated | relid=0 | w=41
  45. en:leucinosis -- r_associated #0: 41 / 0.788 -> en:jankovic rivera syndrome
    n1=en:leucinosis | n2=en:jankovic rivera syndrome | rel=r_associated | relid=0 | w=41
  46. en:leucinosis -- r_associated #0: 41 / 0.788 -> en:laurence-moon syndrome
    n1=en:leucinosis | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=41
  47. en:leucinosis -- r_associated #0: 41 / 0.788 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome
    n1=en:leucinosis | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=41
  48. en:leucinosis -- r_associated #0: 41 / 0.788 -> en:newborn conditions with equivocal markers:prid:pt:bld.dot:nom
    n1=en:leucinosis | n2=en:newborn conditions with equivocal markers:prid:pt:bld.dot:nom | rel=r_associated | relid=0 | w=41
  49. en:leucinosis -- r_associated #0: 41 / 0.788 -> en:renal tubulopathy with encephalopathy and liver failure syndrome
    n1=en:leucinosis | n2=en:renal tubulopathy with encephalopathy and liver failure syndrome | rel=r_associated | relid=0 | w=41
  50. en:leucinosis -- r_associated #0: 41 / 0.788 -> en:staphylococcal scalded skin syndrome
    n1=en:leucinosis | n2=en:staphylococcal scalded skin syndrome | rel=r_associated | relid=0 | w=41
  51. en:leucinosis -- r_associated #0: 41 / 0.788 -> en:sulfite oxidase deficiency
    n1=en:leucinosis | n2=en:sulfite oxidase deficiency | rel=r_associated | relid=0 | w=41
  52. en:leucinosis -- r_associated #0: 41 / 0.788 -> en:weill-marchesani syndrome
    n1=en:leucinosis | n2=en:weill-marchesani syndrome | rel=r_associated | relid=0 | w=41
  53. en:leucinosis -- r_associated #0: 40 / 0.769 -> chromosome 19
    n1=en:leucinosis | n2=chromosome 19 | rel=r_associated | relid=0 | w=40
  54. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:17-beta-hydroxysteroid dehydrogenase 3 deficiency
    n1=en:leucinosis | n2=en:17-beta-hydroxysteroid dehydrogenase 3 deficiency | rel=r_associated | relid=0 | w=40
  55. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:3-methylglutaconic aciduria type 1
    n1=en:leucinosis | n2=en:3-methylglutaconic aciduria type 1 | rel=r_associated | relid=0 | w=40
  56. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:alstrom syndrome
    n1=en:leucinosis | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=40
  57. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:anemia, hypochromic microcytic, with iron overload
    n1=en:leucinosis | n2=en:anemia, hypochromic microcytic, with iron overload | rel=r_associated | relid=0 | w=40
  58. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:autosomal hereditary disorder
    n1=en:leucinosis | n2=en:autosomal hereditary disorder | rel=r_associated | relid=0 | w=40
  59. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:autosomal recessive disorder
    n1=en:leucinosis | n2=en:autosomal recessive disorder | rel=r_associated | relid=0 | w=40
  60. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:bannayan syndrome
    n1=en:leucinosis | n2=en:bannayan syndrome | rel=r_associated | relid=0 | w=40
  61. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:butyryl-coa dehydrogenase deficiency
    n1=en:leucinosis | n2=en:butyryl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=40
  62. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:caused by mutation in the branched chain keto acid dehydrogenase e1, alpha polypeptide gene (bckdha, 608348.0001)
    n1=en:leucinosis | n2=en:caused by mutation in the branched chain keto acid dehydrogenase e1, alpha polypeptide gene (bckdha, 608348.0001) | rel=r_associated | relid=0 | w=40
  63. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:cogan-reese syndrome
    n1=en:leucinosis | n2=en:cogan-reese syndrome | rel=r_associated | relid=0 | w=40
  64. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:complete mevalonate kinase deficiency
    n1=en:leucinosis | n2=en:complete mevalonate kinase deficiency | rel=r_associated | relid=0 | w=40
  65. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:congenital combined immunodeficiency
    n1=en:leucinosis | n2=en:congenital combined immunodeficiency | rel=r_associated | relid=0 | w=40
  66. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:cystinuria
    n1=en:leucinosis | n2=en:cystinuria | rel=r_associated | relid=0 | w=40
  67. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:desmosterolosis
    n1=en:leucinosis | n2=en:desmosterolosis | rel=r_associated | relid=0 | w=40
  68. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:disorder due to n-acetyltransferase enzyme variant
    n1=en:leucinosis | n2=en:disorder due to n-acetyltransferase enzyme variant | rel=r_associated | relid=0 | w=40
  69. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:ebstein anomaly
    n1=en:leucinosis | n2=en:ebstein anomaly | rel=r_associated | relid=0 | w=40
  70. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:encephalopathy due to sulfite oxidase deficiency
    n1=en:leucinosis | n2=en:encephalopathy due to sulfite oxidase deficiency | rel=r_associated | relid=0 | w=40
  71. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:epidemiologic
    n1=en:leucinosis | n2=en:epidemiologic | rel=r_associated | relid=0 | w=40
  72. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:exposure as collected domain
    n1=en:leucinosis | n2=en:exposure as collected domain | rel=r_associated | relid=0 | w=40
  73. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:familial acute myeloid leukemia
    n1=en:leucinosis | n2=en:familial acute myeloid leukemia | rel=r_associated | relid=0 | w=40
  74. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:familial amyloidosis
    n1=en:leucinosis | n2=en:familial amyloidosis | rel=r_associated | relid=0 | w=40
  75. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:familial hypercalciuric hypocalcemia
    n1=en:leucinosis | n2=en:familial hypercalciuric hypocalcemia | rel=r_associated | relid=0 | w=40
  76. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:fanconi syndrome
    n1=en:leucinosis | n2=en:fanconi syndrome | rel=r_associated | relid=0 | w=40
  77. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:fatty acid metabolism disorder
    n1=en:leucinosis | n2=en:fatty acid metabolism disorder | rel=r_associated | relid=0 | w=40
  78. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:fibrodysplasia ossificans progressiva
    n1=en:leucinosis | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=40
  79. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:fibromuscular dysplasia
    n1=en:leucinosis | n2=en:fibromuscular dysplasia | rel=r_associated | relid=0 | w=40
  80. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:fox-fordyce disease
    n1=en:leucinosis | n2=en:fox-fordyce disease | rel=r_associated | relid=0 | w=40
  81. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:gamma-glutamyltransferase deficiency
    n1=en:leucinosis | n2=en:gamma-glutamyltransferase deficiency | rel=r_associated | relid=0 | w=40
  82. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:generalized arterial calcification of infancy 1
    n1=en:leucinosis | n2=en:generalized arterial calcification of infancy 1 | rel=r_associated | relid=0 | w=40
  83. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:glucose-6-phosphate dehydrogenase deficiency anemia
    n1=en:leucinosis | n2=en:glucose-6-phosphate dehydrogenase deficiency anemia | rel=r_associated | relid=0 | w=40
  84. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:hereditary hyperbilirubinemia
    n1=en:leucinosis | n2=en:hereditary hyperbilirubinemia | rel=r_associated | relid=0 | w=40
  85. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:hereditary leiomyomatosis and renal cell cancer
    n1=en:leucinosis | n2=en:hereditary leiomyomatosis and renal cell cancer | rel=r_associated | relid=0 | w=40
  86. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:hereditary neoplastic syndrome
    n1=en:leucinosis | n2=en:hereditary neoplastic syndrome | rel=r_associated | relid=0 | w=40
  87. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:hereditary persistence of fetal hemoglobin
    n1=en:leucinosis | n2=en:hereditary persistence of fetal hemoglobin | rel=r_associated | relid=0 | w=40
  88. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:hmg-coa lyase deficiency
    n1=en:leucinosis | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=40
  89. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:holocarboxylase synthetase deficiency
    n1=en:leucinosis | n2=en:holocarboxylase synthetase deficiency | rel=r_associated | relid=0 | w=40
  90. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:homocystinuria
    n1=en:leucinosis | n2=en:homocystinuria | rel=r_associated | relid=0 | w=40
  91. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:hyperlysinemia
    n1=en:leucinosis | n2=en:hyperlysinemia | rel=r_associated | relid=0 | w=40
  92. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:hyperphenylalaninemia
    n1=en:leucinosis | n2=en:hyperphenylalaninemia | rel=r_associated | relid=0 | w=40
  93. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:hyperphosphatasia with mental retardation
    n1=en:leucinosis | n2=en:hyperphosphatasia with mental retardation | rel=r_associated | relid=0 | w=40
  94. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:hyperprolinemia type 2
    n1=en:leucinosis | n2=en:hyperprolinemia type 2 | rel=r_associated | relid=0 | w=40
  95. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:hypomyelination and congenital cataract
    n1=en:leucinosis | n2=en:hypomyelination and congenital cataract | rel=r_associated | relid=0 | w=40
  96. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:immunodeficiency with hyper-igm type 2
    n1=en:leucinosis | n2=en:immunodeficiency with hyper-igm type 2 | rel=r_associated | relid=0 | w=40
  97. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:immunology aspects
    n1=en:leucinosis | n2=en:immunology aspects | rel=r_associated | relid=0 | w=40
  98. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:inborn error of lipoprotein metabolism
    n1=en:leucinosis | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=40
  99. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:infantile refsum disease
    n1=en:leucinosis | n2=en:infantile refsum disease | rel=r_associated | relid=0 | w=40
  100. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:insulin growth factor i resistance
    n1=en:leucinosis | n2=en:insulin growth factor i resistance | rel=r_associated | relid=0 | w=40
  101. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:intermediary metabolism disorder
    n1=en:leucinosis | n2=en:intermediary metabolism disorder | rel=r_associated | relid=0 | w=40
  102. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:joubert syndrome
    n1=en:leucinosis | n2=en:joubert syndrome | rel=r_associated | relid=0 | w=40
  103. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:lethal congenital contracture syndrome 1
    n1=en:leucinosis | n2=en:lethal congenital contracture syndrome 1 | rel=r_associated | relid=0 | w=40
  104. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
    n1=en:leucinosis | n2=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | rel=r_associated | relid=0 | w=40
  105. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:lig4 syndrome
    n1=en:leucinosis | n2=en:lig4 syndrome | rel=r_associated | relid=0 | w=40
  106. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:lipid metabolism, inborn errors
    n1=en:leucinosis | n2=en:lipid metabolism, inborn errors | rel=r_associated | relid=0 | w=40
  107. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:lysosomal storage diseases, nervous system
    n1=en:leucinosis | n2=en:lysosomal storage diseases, nervous system | rel=r_associated | relid=0 | w=40
  108. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:maple syrup urine disease, e3 deficient, with lactic acidosis
    n1=en:leucinosis | n2=en:maple syrup urine disease, e3 deficient, with lactic acidosis | rel=r_associated | relid=0 | w=40
  109. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:merrf syndrome
    n1=en:leucinosis | n2=en:merrf syndrome | rel=r_associated | relid=0 | w=40
  110. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:metal metabolism, inborn errors
    n1=en:leucinosis | n2=en:metal metabolism, inborn errors | rel=r_associated | relid=0 | w=40
  111. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:moderate mental retardation (i.q. 35-49)
    n1=en:leucinosis | n2=en:moderate mental retardation (i.q. 35-49) | rel=r_associated | relid=0 | w=40
  112. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:morm syndrome
    n1=en:leucinosis | n2=en:morm syndrome | rel=r_associated | relid=0 | w=40
  113. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:mucopolysaccharidosis type i
    n1=en:leucinosis | n2=en:mucopolysaccharidosis type i | rel=r_associated | relid=0 | w=40
  114. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:muenke syndrome
    n1=en:leucinosis | n2=en:muenke syndrome | rel=r_associated | relid=0 | w=40
  115. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:mulibrey nanism
    n1=en:leucinosis | n2=en:mulibrey nanism | rel=r_associated | relid=0 | w=40
  116. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:mullerian inhibiting factor deficiency
    n1=en:leucinosis | n2=en:mullerian inhibiting factor deficiency | rel=r_associated | relid=0 | w=40
  117. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:multicentric osteolysis nodulosis arthropathy spectrum
    n1=en:leucinosis | n2=en:multicentric osteolysis nodulosis arthropathy spectrum | rel=r_associated | relid=0 | w=40
  118. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:myopathy, early-onset, with fatal cardiomyopathy
    n1=en:leucinosis | n2=en:myopathy, early-onset, with fatal cardiomyopathy | rel=r_associated | relid=0 | w=40
  119. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:myotonic disorder
    n1=en:leucinosis | n2=en:myotonic disorder | rel=r_associated | relid=0 | w=40
  120. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:naxos disease
    n1=en:leucinosis | n2=en:naxos disease | rel=r_associated | relid=0 | w=40
  121. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:neurodegeneration due to cerebral folate transport deficiency
    n1=en:leucinosis | n2=en:neurodegeneration due to cerebral folate transport deficiency | rel=r_associated | relid=0 | w=40
  122. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:oculocerebral hypopigmentation syndrome type preus
    n1=en:leucinosis | n2=en:oculocerebral hypopigmentation syndrome type preus | rel=r_associated | relid=0 | w=40
  123. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:osteochondrodysplasia
    n1=en:leucinosis | n2=en:osteochondrodysplasia | rel=r_associated | relid=0 | w=40
  124. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:other specified disorders of amino-acid metabolism
    n1=en:leucinosis | n2=en:other specified disorders of amino-acid metabolism | rel=r_associated | relid=0 | w=40
  125. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:pancreatic lipase deficiency
    n1=en:leucinosis | n2=en:pancreatic lipase deficiency | rel=r_associated | relid=0 | w=40
  126. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:pancreatic triacylglycerol lipase deficiency
    n1=en:leucinosis | n2=en:pancreatic triacylglycerol lipase deficiency | rel=r_associated | relid=0 | w=40
  127. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:pathological aspects
    n1=en:leucinosis | n2=en:pathological aspects | rel=r_associated | relid=0 | w=40
  128. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:peeling skin syndrome, acral type
    n1=en:leucinosis | n2=en:peeling skin syndrome, acral type | rel=r_associated | relid=0 | w=40
  129. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:peroxisomal disorder
    n1=en:leucinosis | n2=en:peroxisomal disorder | rel=r_associated | relid=0 | w=40
  130. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:placental steroid sulfatase deficiency
    n1=en:leucinosis | n2=en:placental steroid sulfatase deficiency | rel=r_associated | relid=0 | w=40
  131. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
    n1=en:leucinosis | n2=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | rel=r_associated | relid=0 | w=40
  132. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:prickle1-related progressive myoclonus epilepsy with ataxia
    n1=en:leucinosis | n2=en:prickle1-related progressive myoclonus epilepsy with ataxia | rel=r_associated | relid=0 | w=40
  133. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:progeria
    n1=en:leucinosis | n2=en:progeria | rel=r_associated | relid=0 | w=40
  134. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:prolidase deficiency
    n1=en:leucinosis | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=40
  135. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:prolonged electroretinal response suppression
    n1=en:leucinosis | n2=en:prolonged electroretinal response suppression | rel=r_associated | relid=0 | w=40
  136. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:prune belly syndrome
    n1=en:leucinosis | n2=en:prune belly syndrome | rel=r_associated | relid=0 | w=40
  137. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:pseudotumor cerebri
    n1=en:leucinosis | n2=en:pseudotumor cerebri | rel=r_associated | relid=0 | w=40
  138. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:purine-pyrimidine metabolism, inborn errors
    n1=en:leucinosis | n2=en:purine-pyrimidine metabolism, inborn errors | rel=r_associated | relid=0 | w=40
  139. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:radioulnar synostosis
    n1=en:leucinosis | n2=en:radioulnar synostosis | rel=r_associated | relid=0 | w=40
  140. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:rapadilino syndrome
    n1=en:leucinosis | n2=en:rapadilino syndrome | rel=r_associated | relid=0 | w=40
  141. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:rothmund-thomson syndrome
    n1=en:leucinosis | n2=en:rothmund-thomson syndrome | rel=r_associated | relid=0 | w=40
  142. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:sanfilippo syndrome
    n1=en:leucinosis | n2=en:sanfilippo syndrome | rel=r_associated | relid=0 | w=40
  143. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:sarcosinemia
    n1=en:leucinosis | n2=en:sarcosinemia | rel=r_associated | relid=0 | w=40
  144. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:specific enzyme deficiency
    n1=en:leucinosis | n2=en:specific enzyme deficiency | rel=r_associated | relid=0 | w=40
  145. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:spinal muscular atrophy with respiratory distress 1
    n1=en:leucinosis | n2=en:spinal muscular atrophy with respiratory distress 1 | rel=r_associated | relid=0 | w=40
  146. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:spondyloenchondrodysplasia
    n1=en:leucinosis | n2=en:spondyloenchondrodysplasia | rel=r_associated | relid=0 | w=40
  147. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:superior mesenteric artery syndrome
    n1=en:leucinosis | n2=en:superior mesenteric artery syndrome | rel=r_associated | relid=0 | w=40
  148. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:synpolydactyly
    n1=en:leucinosis | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=40
  149. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:thiamin-responsive maple syrup urine disease
    n1=en:leucinosis | n2=en:thiamin-responsive maple syrup urine disease | rel=r_associated | relid=0 | w=40
  150. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:thoracic outlet syndrome
    n1=en:leucinosis | n2=en:thoracic outlet syndrome | rel=r_associated | relid=0 | w=40
  151. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:thyroid dyshormonogenesis 4
    n1=en:leucinosis | n2=en:thyroid dyshormonogenesis 4 | rel=r_associated | relid=0 | w=40
  152. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:tolosa-hunt syndrome
    n1=en:leucinosis | n2=en:tolosa-hunt syndrome | rel=r_associated | relid=0 | w=40
  153. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:type ii acrocephalopolysyndactyly
    n1=en:leucinosis | n2=en:type ii acrocephalopolysyndactyly | rel=r_associated | relid=0 | w=40
  154. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment
    n1=en:leucinosis | n2=en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment | rel=r_associated | relid=0 | w=40
  155. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:urine
    n1=en:leucinosis | n2=en:urine | rel=r_associated | relid=0 | w=40
  156. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:west syndrome
    n1=en:leucinosis | n2=en:west syndrome | rel=r_associated | relid=0 | w=40
  157. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:x-linked dominant hypophosphatemic rickets
    n1=en:leucinosis | n2=en:x-linked dominant hypophosphatemic rickets | rel=r_associated | relid=0 | w=40
  158. en:leucinosis -- r_associated #0: 40 / 0.769 -> en:xeroderma pigmentosum
    n1=en:leucinosis | n2=en:xeroderma pigmentosum | rel=r_associated | relid=0 | w=40
  159. en:leucinosis -- r_associated #0: 40 / 0.769 -> leucinose classique
    n1=en:leucinosis | n2=leucinose classique | rel=r_associated | relid=0 | w=40
  160. en:leucinosis -- r_associated #0: 40 / 0.769 -> maladie du $organe$
    n1=en:leucinosis | n2=maladie du $organe$ | rel=r_associated | relid=0 | w=40
  161. en:leucinosis -- r_associated #0: 40 / 0.769 -> maladies des urines avec odeur de sirop erable
    n1=en:leucinosis | n2=maladies des urines avec odeur de sirop erable | rel=r_associated | relid=0 | w=40
  162. en:leucinosis -- r_associated #0: 40 / 0.769 -> maladies génétiques du métabolisme des acides aminés
    n1=en:leucinosis | n2=maladies génétiques du métabolisme des acides aminés | rel=r_associated | relid=0 | w=40
  163. en:leucinosis -- r_associated #0: 40 / 0.769 -> processus pathologique
    n1=en:leucinosis | n2=processus pathologique | rel=r_associated | relid=0 | w=40
  164. en:leucinosis -- r_associated #0: 39 / 0.75 -> acide
    n1=en:leucinosis | n2=acide | rel=r_associated | relid=0 | w=39
  165. en:leucinosis -- r_associated #0: 39 / 0.75 -> acide aminé
    n1=en:leucinosis | n2=acide aminé | rel=r_associated | relid=0 | w=39
  166. en:leucinosis -- r_associated #0: 39 / 0.75 -> déficit
    n1=en:leucinosis | n2=déficit | rel=r_associated | relid=0 | w=39
  167. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:(3) intermediate
    n1=en:leucinosis | n2=en:(3) intermediate | rel=r_associated | relid=0 | w=39
  168. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:17q21 microdeletion syndrome
    n1=en:leucinosis | n2=en:17q21 microdeletion syndrome | rel=r_associated | relid=0 | w=39
  169. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:3-methylglutaconic aciduria type 5
    n1=en:leucinosis | n2=en:3-methylglutaconic aciduria type 5 | rel=r_associated | relid=0 | w=39
  170. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:achondroplasia
    n1=en:leucinosis | n2=en:achondroplasia | rel=r_associated | relid=0 | w=39
  171. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:achromatopsia
    n1=en:leucinosis | n2=en:achromatopsia | rel=r_associated | relid=0 | w=39
  172. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:acyl-coa dehydrogenase, short-chain deficiency
    n1=en:leucinosis | n2=en:acyl-coa dehydrogenase, short-chain deficiency | rel=r_associated | relid=0 | w=39
  173. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:adrenoleukodystrophy
    n1=en:leucinosis | n2=en:adrenoleukodystrophy | rel=r_associated | relid=0 | w=39
  174. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:adult hypophosphatasia (disorder)
    n1=en:leucinosis | n2=en:adult hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=39
  175. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:agnosia
    n1=en:leucinosis | n2=en:agnosia | rel=r_associated | relid=0 | w=39
  176. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:amino acid metabolism disorder
    n1=en:leucinosis | n2=en:amino acid metabolism disorder | rel=r_associated | relid=0 | w=39
  177. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:amino acid transport disorders, inborn
    n1=en:leucinosis | n2=en:amino acid transport disorders, inborn | rel=r_associated | relid=0 | w=39
  178. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:amino acids, branched-chain
    n1=en:leucinosis | n2=en:amino acids, branched-chain | rel=r_associated | relid=0 | w=39
  179. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:aminoacylase 1 deficiency
    n1=en:leucinosis | n2=en:aminoacylase 1 deficiency | rel=r_associated | relid=0 | w=39
  180. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:aminomethyltransferase deficiency
    n1=en:leucinosis | n2=en:aminomethyltransferase deficiency | rel=r_associated | relid=0 | w=39
  181. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:amniotic band syndrome
    n1=en:leucinosis | n2=en:amniotic band syndrome | rel=r_associated | relid=0 | w=39
  182. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:angelman syndrome
    n1=en:leucinosis | n2=en:angelman syndrome | rel=r_associated | relid=0 | w=39
  183. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:anhidrotic ectodermal dysplasia 1
    n1=en:leucinosis | n2=en:anhidrotic ectodermal dysplasia 1 | rel=r_associated | relid=0 | w=39
  184. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:antley-bixler syndrome, autosomal dominant
    n1=en:leucinosis | n2=en:antley-bixler syndrome, autosomal dominant | rel=r_associated | relid=0 | w=39
  185. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:atransferrinemia
    n1=en:leucinosis | n2=en:atransferrinemia | rel=r_associated | relid=0 | w=39
  186. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:autosomal recessive primary microcephaly
    n1=en:leucinosis | n2=en:autosomal recessive primary microcephaly | rel=r_associated | relid=0 | w=39
  187. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:autosomal recessive scid
    n1=en:leucinosis | n2=en:autosomal recessive scid | rel=r_associated | relid=0 | w=39
  188. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:autosomal recessive trait
    n1=en:leucinosis | n2=en:autosomal recessive trait | rel=r_associated | relid=0 | w=39
  189. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:bardet-biedl syndrome
    n1=en:leucinosis | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=39
  190. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:bckdhb gene
    n1=en:leucinosis | n2=en:bckdhb gene | rel=r_associated | relid=0 | w=39
  191. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:beckwith-wiedemann syndrome
    n1=en:leucinosis | n2=en:beckwith-wiedemann syndrome | rel=r_associated | relid=0 | w=39
  192. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:bernard-soulier syndrome
    n1=en:leucinosis | n2=en:bernard-soulier syndrome | rel=r_associated | relid=0 | w=39
  193. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:beta-aminoisobutyricaciduria
    n1=en:leucinosis | n2=en:beta-aminoisobutyricaciduria | rel=r_associated | relid=0 | w=39
  194. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:beta-methylcrotonylglycinuria
    n1=en:leucinosis | n2=en:beta-methylcrotonylglycinuria | rel=r_associated | relid=0 | w=39
  195. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:brain iron accumulation type i syndrome
    n1=en:leucinosis | n2=en:brain iron accumulation type i syndrome | rel=r_associated | relid=0 | w=39
  196. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:cerebellar ataxia ectodermal dysplasia
    n1=en:leucinosis | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=39
  197. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:chemically induced
    n1=en:leucinosis | n2=en:chemically induced | rel=r_associated | relid=0 | w=39
  198. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:chondrodysplasia punctata
    n1=en:leucinosis | n2=en:chondrodysplasia punctata | rel=r_associated | relid=0 | w=39
  199. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:chondrodysplasia punctata syndrome
    n1=en:leucinosis | n2=en:chondrodysplasia punctata syndrome | rel=r_associated | relid=0 | w=39
  200. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:chromosome 2q37 deletion syndrome
    n1=en:leucinosis | n2=en:chromosome 2q37 deletion syndrome | rel=r_associated | relid=0 | w=39
  201. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:cleft lip/palate-ectodermal dysplasia syndrome
    n1=en:leucinosis | n2=en:cleft lip/palate-ectodermal dysplasia syndrome | rel=r_associated | relid=0 | w=39
  202. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:coma
    n1=en:leucinosis | n2=en:coma | rel=r_associated | relid=0 | w=39
  203. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:congenital cortical hyperostosis
    n1=en:leucinosis | n2=en:congenital cortical hyperostosis | rel=r_associated | relid=0 | w=39
  204. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:congenital insensitivity to pain with anhidrosis
    n1=en:leucinosis | n2=en:congenital insensitivity to pain with anhidrosis | rel=r_associated | relid=0 | w=39
  205. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:congenital leucocyte abnormality
    n1=en:leucinosis | n2=en:congenital leucocyte abnormality | rel=r_associated | relid=0 | w=39
  206. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:congenital transferrin deficiency
    n1=en:leucinosis | n2=en:congenital transferrin deficiency | rel=r_associated | relid=0 | w=39
  207. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:cystic fibrosis
    n1=en:leucinosis | n2=en:cystic fibrosis | rel=r_associated | relid=0 | w=39
  208. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:darier disease
    n1=en:leucinosis | n2=en:darier disease | rel=r_associated | relid=0 | w=39
  209. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:deafness, autosomal recessive 28
    n1=en:leucinosis | n2=en:deafness, autosomal recessive 28 | rel=r_associated | relid=0 | w=39
  210. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:deficiency in enzyme complexes of mitochondrial respiratory chain
    n1=en:leucinosis | n2=en:deficiency in enzyme complexes of mitochondrial respiratory chain | rel=r_associated | relid=0 | w=39
  211. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:dicarboxylicaminoaciduria
    n1=en:leucinosis | n2=en:dicarboxylicaminoaciduria | rel=r_associated | relid=0 | w=39
  212. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:dihydropyrimidinase deficiency
    n1=en:leucinosis | n2=en:dihydropyrimidinase deficiency | rel=r_associated | relid=0 | w=39
  213. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:dihydropyrimidine dehydrogenase deficiency
    n1=en:leucinosis | n2=en:dihydropyrimidine dehydrogenase deficiency | rel=r_associated | relid=0 | w=39
  214. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:disorder of glycoprotein metabolism
    n1=en:leucinosis | n2=en:disorder of glycoprotein metabolism | rel=r_associated | relid=0 | w=39
  215. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:disorder of sulfur-bearing amino acid metabolism
    n1=en:leucinosis | n2=en:disorder of sulfur-bearing amino acid metabolism | rel=r_associated | relid=0 | w=39
  216. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:donohue syndrome
    n1=en:leucinosis | n2=en:donohue syndrome | rel=r_associated | relid=0 | w=39
  217. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:dyggve-melchior-clausen syndrome
    n1=en:leucinosis | n2=en:dyggve-melchior-clausen syndrome | rel=r_associated | relid=0 | w=39
  218. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:dyschromatosis symmetrica hereditaria
    n1=en:leucinosis | n2=en:dyschromatosis symmetrica hereditaria | rel=r_associated | relid=0 | w=39
  219. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:ellis-van creveld syndrome
    n1=en:leucinosis | n2=en:ellis-van creveld syndrome | rel=r_associated | relid=0 | w=39
  220. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:epidermolysis bullosa
    n1=en:leucinosis | n2=en:epidermolysis bullosa | rel=r_associated | relid=0 | w=39
  221. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:familial carcinoid syndrome
    n1=en:leucinosis | n2=en:familial carcinoid syndrome | rel=r_associated | relid=0 | w=39
  222. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:familial mediterranean fever
    n1=en:leucinosis | n2=en:familial mediterranean fever | rel=r_associated | relid=0 | w=39
  223. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:familial partial lipodystrophy
    n1=en:leucinosis | n2=en:familial partial lipodystrophy | rel=r_associated | relid=0 | w=39
  224. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:felty syndrome
    n1=en:leucinosis | n2=en:felty syndrome | rel=r_associated | relid=0 | w=39
  225. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:friedreich ataxia
    n1=en:leucinosis | n2=en:friedreich ataxia | rel=r_associated | relid=0 | w=39
  226. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:generalized myotonia of thomsen
    n1=en:leucinosis | n2=en:generalized myotonia of thomsen | rel=r_associated | relid=0 | w=39
  227. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:glanzmann thrombasthenia
    n1=en:leucinosis | n2=en:glanzmann thrombasthenia | rel=r_associated | relid=0 | w=39
  228. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:glucose-6-phosphate dehydrogenase deficiency
    n1=en:leucinosis | n2=en:glucose-6-phosphate dehydrogenase deficiency | rel=r_associated | relid=0 | w=39
  229. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:glycogen storage disease type x
    n1=en:leucinosis | n2=en:glycogen storage disease type x | rel=r_associated | relid=0 | w=39
  230. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:goniodysgenesis-mental retardation-short stature syndrome
    n1=en:leucinosis | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=39
  231. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:hajdu-cheney syndrome
    n1=en:leucinosis | n2=en:hajdu-cheney syndrome | rel=r_associated | relid=0 | w=39
  232. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:hereditary adrenal unresponsiveness to corticotropin
    n1=en:leucinosis | n2=en:hereditary adrenal unresponsiveness to corticotropin | rel=r_associated | relid=0 | w=39
  233. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:hereditary disease in family possibly affecting fetus, affecting management of mother, antepartum condition or complication
    n1=en:leucinosis | n2=en:hereditary disease in family possibly affecting fetus, affecting management of mother, antepartum condition or complication | rel=r_associated | relid=0 | w=39
  234. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:hereditary disease in family possibly affecting fetus, affecting management of mother, unspecified as to episode of care in pregnancy
    n1=en:leucinosis | n2=en:hereditary disease in family possibly affecting fetus, affecting management of mother, unspecified as to episode of care in pregnancy | rel=r_associated | relid=0 | w=39
  235. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:hereditary gastrointestinal stromal tumor
    n1=en:leucinosis | n2=en:hereditary gastrointestinal stromal tumor | rel=r_associated | relid=0 | w=39
  236. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:hereditary motor end-plate disease
    n1=en:leucinosis | n2=en:hereditary motor end-plate disease | rel=r_associated | relid=0 | w=39
  237. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:hereditary xanthinuria
    n1=en:leucinosis | n2=en:hereditary xanthinuria | rel=r_associated | relid=0 | w=39
  238. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:hermansky-pudlak syndrome
    n1=en:leucinosis | n2=en:hermansky-pudlak syndrome | rel=r_associated | relid=0 | w=39
  239. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:hyaline membrane syndrome
    n1=en:leucinosis | n2=en:hyaline membrane syndrome | rel=r_associated | relid=0 | w=39
  240. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:hyperkalemic periodic paralysis
    n1=en:leucinosis | n2=en:hyperkalemic periodic paralysis | rel=r_associated | relid=0 | w=39
  241. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:hyperphenylalaninemia, non phenylketonuric
    n1=en:leucinosis | n2=en:hyperphenylalaninemia, non phenylketonuric | rel=r_associated | relid=0 | w=39
  242. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:hypoglycemia
    n1=en:leucinosis | n2=en:hypoglycemia | rel=r_associated | relid=0 | w=39
  243. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:idiopathic cd4-positive t-lymphocytopenia
    n1=en:leucinosis | n2=en:idiopathic cd4-positive t-lymphocytopenia | rel=r_associated | relid=0 | w=39
  244. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:inborn immunodeficiency
    n1=en:leucinosis | n2=en:inborn immunodeficiency | rel=r_associated | relid=0 | w=39
  245. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:incontinentia pigmenti
    n1=en:leucinosis | n2=en:incontinentia pigmenti | rel=r_associated | relid=0 | w=39
  246. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:intestinal atresia
    n1=en:leucinosis | n2=en:intestinal atresia | rel=r_associated | relid=0 | w=39
  247. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:jacobsen syndrome
    n1=en:leucinosis | n2=en:jacobsen syndrome | rel=r_associated | relid=0 | w=39
  248. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:ketosis
    n1=en:leucinosis | n2=en:ketosis | rel=r_associated | relid=0 | w=39
  249. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:kimura disease
    n1=en:leucinosis | n2=en:kimura disease | rel=r_associated | relid=0 | w=39
  250. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:lafora disease
    n1=en:leucinosis | n2=en:lafora disease | rel=r_associated | relid=0 | w=39
  251. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:leber congenital amaurosis
    n1=en:leucinosis | n2=en:leber congenital amaurosis | rel=r_associated | relid=0 | w=39
  252. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:leopard syndrome
    n1=en:leucinosis | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=39
  253. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:leukodystrophy
    n1=en:leucinosis | n2=en:leukodystrophy | rel=r_associated | relid=0 | w=39
  254. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:lissencephaly syndrome, norman-roberts type
    n1=en:leucinosis | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=39
  255. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:lynch syndrome
    n1=en:leucinosis | n2=en:lynch syndrome | rel=r_associated | relid=0 | w=39
  256. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:lysinuric protein intolerance
    n1=en:leucinosis | n2=en:lysinuric protein intolerance | rel=r_associated | relid=0 | w=39
  257. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:macdermot winter syndrome
    n1=en:leucinosis | n2=en:macdermot winter syndrome | rel=r_associated | relid=0 | w=39
  258. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:macular corneal dystrophy
    n1=en:leucinosis | n2=en:macular corneal dystrophy | rel=r_associated | relid=0 | w=39
  259. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:mallory-weiss syndrome
    n1=en:leucinosis | n2=en:mallory-weiss syndrome | rel=r_associated | relid=0 | w=39
  260. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:medium-chain acyl-coa dehydrogenase deficiency
    n1=en:leucinosis | n2=en:medium-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=39
  261. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:methylcrotonyl-coa carboxylase deficiency
    n1=en:leucinosis | n2=en:methylcrotonyl-coa carboxylase deficiency | rel=r_associated | relid=0 | w=39
  262. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:microphthalmia, syndromic 4 (disorder)
    n1=en:leucinosis | n2=en:microphthalmia, syndromic 4 (disorder) | rel=r_associated | relid=0 | w=39
  263. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:n-methylsuccinimide
    n1=en:leucinosis | n2=en:n-methylsuccinimide | rel=r_associated | relid=0 | w=39
  264. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:nadh dehydrogenase deficiency
    n1=en:leucinosis | n2=en:nadh dehydrogenase deficiency | rel=r_associated | relid=0 | w=39
  265. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:nephrogenic fibrosing dermopathy
    n1=en:leucinosis | n2=en:nephrogenic fibrosing dermopathy | rel=r_associated | relid=0 | w=39
  266. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:neurofibromatosis
    n1=en:leucinosis | n2=en:neurofibromatosis | rel=r_associated | relid=0 | w=39
  267. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:neuronal intranuclear inclusion disease
    n1=en:leucinosis | n2=en:neuronal intranuclear inclusion disease | rel=r_associated | relid=0 | w=39
  268. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:non-trisomic autosomal aneuploidy
    n1=en:leucinosis | n2=en:non-trisomic autosomal aneuploidy | rel=r_associated | relid=0 | w=39
  269. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:oculootoradial syndrome
    n1=en:leucinosis | n2=en:oculootoradial syndrome | rel=r_associated | relid=0 | w=39
  270. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:oeis complex
    n1=en:leucinosis | n2=en:oeis complex | rel=r_associated | relid=0 | w=39
  271. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:optic neuritis
    n1=en:leucinosis | n2=en:optic neuritis | rel=r_associated | relid=0 | w=39
  272. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:otoonychoperoneal syndrome
    n1=en:leucinosis | n2=en:otoonychoperoneal syndrome | rel=r_associated | relid=0 | w=39
  273. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:pachyonychia congenita
    n1=en:leucinosis | n2=en:pachyonychia congenita | rel=r_associated | relid=0 | w=39
  274. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:pallister-killian syndrome
    n1=en:leucinosis | n2=en:pallister-killian syndrome | rel=r_associated | relid=0 | w=39
  275. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:panuveitis
    n1=en:leucinosis | n2=en:panuveitis | rel=r_associated | relid=0 | w=39
  276. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:piriformis muscle syndrome
    n1=en:leucinosis | n2=en:piriformis muscle syndrome | rel=r_associated | relid=0 | w=39
  277. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:pityriasis lichenoides
    n1=en:leucinosis | n2=en:pityriasis lichenoides | rel=r_associated | relid=0 | w=39
  278. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:plummer-vinson syndrome
    n1=en:leucinosis | n2=en:plummer-vinson syndrome | rel=r_associated | relid=0 | w=39
  279. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:poland syndrome
    n1=en:leucinosis | n2=en:poland syndrome | rel=r_associated | relid=0 | w=39
  280. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:potocki-shaffer syndrome
    n1=en:leucinosis | n2=en:potocki-shaffer syndrome | rel=r_associated | relid=0 | w=39
  281. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:prosopagnosia
    n1=en:leucinosis | n2=en:prosopagnosia | rel=r_associated | relid=0 | w=39
  282. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:pseudocholinesterase deficiency
    n1=en:leucinosis | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=39
  283. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:pseudohermaphroditism
    n1=en:leucinosis | n2=en:pseudohermaphroditism | rel=r_associated | relid=0 | w=39
  284. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:pseudohypoaldosteronism
    n1=en:leucinosis | n2=en:pseudohypoaldosteronism | rel=r_associated | relid=0 | w=39
  285. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:refsum disease
    n1=en:leucinosis | n2=en:refsum disease | rel=r_associated | relid=0 | w=39
  286. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:renpenning syndrome 1
    n1=en:leucinosis | n2=en:renpenning syndrome 1 | rel=r_associated | relid=0 | w=39
  287. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:rett syndrome, atypical
    n1=en:leucinosis | n2=en:rett syndrome, atypical | rel=r_associated | relid=0 | w=39
  288. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:rhizomelic dysplasia
    n1=en:leucinosis | n2=en:rhizomelic dysplasia | rel=r_associated | relid=0 | w=39
  289. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:richards-rundle syndrome
    n1=en:leucinosis | n2=en:richards-rundle syndrome | rel=r_associated | relid=0 | w=39
  290. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:savant syndrome
    n1=en:leucinosis | n2=en:savant syndrome | rel=r_associated | relid=0 | w=39
  291. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:scleredema adultorum
    n1=en:leucinosis | n2=en:scleredema adultorum | rel=r_associated | relid=0 | w=39
  292. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:severe early childhood onset retinal dystrophy
    n1=en:leucinosis | n2=en:severe early childhood onset retinal dystrophy | rel=r_associated | relid=0 | w=39
  293. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:shwachman-diamond syndrome
    n1=en:leucinosis | n2=en:shwachman-diamond syndrome | rel=r_associated | relid=0 | w=39
  294. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:stargardt disease
    n1=en:leucinosis | n2=en:stargardt disease | rel=r_associated | relid=0 | w=39
  295. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:stiff person syndrome
    n1=en:leucinosis | n2=en:stiff person syndrome | rel=r_associated | relid=0 | w=39
  296. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:thrombocytopenia 2
    n1=en:leucinosis | n2=en:thrombocytopenia 2 | rel=r_associated | relid=0 | w=39
  297. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:tmem70 related mitochondrial encephalo-cardio-myopathy
    n1=en:leucinosis | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=39
  298. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:transitory amino acid metabolic disorder
    n1=en:leucinosis | n2=en:transitory amino acid metabolic disorder | rel=r_associated | relid=0 | w=39
  299. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:treacher collins syndrome
    n1=en:leucinosis | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=39
  300. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:trichinosis
    n1=en:leucinosis | n2=en:trichinosis | rel=r_associated | relid=0 | w=39
  301. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:trichorhinophalangeal syndrome type i
    n1=en:leucinosis | n2=en:trichorhinophalangeal syndrome type i | rel=r_associated | relid=0 | w=39
  302. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:trichorhinophalangeal syndrome type ii
    n1=en:leucinosis | n2=en:trichorhinophalangeal syndrome type ii | rel=r_associated | relid=0 | w=39
  303. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:trisomy 14 mosaicism
    n1=en:leucinosis | n2=en:trisomy 14 mosaicism | rel=r_associated | relid=0 | w=39
  304. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:true hermaphroditism
    n1=en:leucinosis | n2=en:true hermaphroditism | rel=r_associated | relid=0 | w=39
  305. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour
    n1=en:leucinosis | n2=en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour | rel=r_associated | relid=0 | w=39
  306. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:viruses
    n1=en:leucinosis | n2=en:viruses | rel=r_associated | relid=0 | w=39
  307. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:von hippel-lindau syndrome
    n1=en:leucinosis | n2=en:von hippel-lindau syndrome | rel=r_associated | relid=0 | w=39
  308. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:waardenburg syndrome
    n1=en:leucinosis | n2=en:waardenburg syndrome | rel=r_associated | relid=0 | w=39
  309. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:waisman syndrome
    n1=en:leucinosis | n2=en:waisman syndrome | rel=r_associated | relid=0 | w=39
  310. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:werdnig-hoffmann disease
    n1=en:leucinosis | n2=en:werdnig-hoffmann disease | rel=r_associated | relid=0 | w=39
  311. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:whipple disease
    n1=en:leucinosis | n2=en:whipple disease | rel=r_associated | relid=0 | w=39
  312. en:leucinosis -- r_associated #0: 39 / 0.75 -> en:williams syndrome
    n1=en:leucinosis | n2=en:williams syndrome | rel=r_associated | relid=0 | w=39
  313. en:leucinosis -- r_associated #0: 39 / 0.75 -> maladies rares
    n1=en:leucinosis | n2=maladies rares | rel=r_associated | relid=0 | w=39
  314. en:leucinosis -- r_associated #0: 39 / 0.75 -> médecine
    n1=en:leucinosis | n2=médecine | rel=r_associated | relid=0 | w=39
  315. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:1p36 deletion syndrome
    n1=en:leucinosis | n2=en:1p36 deletion syndrome | rel=r_associated | relid=0 | w=38
  316. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:3-methylglutaconic aciduria type iv
    n1=en:leucinosis | n2=en:3-methylglutaconic aciduria type iv | rel=r_associated | relid=0 | w=38
  317. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:acatalasemia
    n1=en:leucinosis | n2=en:acatalasemia | rel=r_associated | relid=0 | w=38
  318. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:adiposis dolorosa
    n1=en:leucinosis | n2=en:adiposis dolorosa | rel=r_associated | relid=0 | w=38
  319. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:adrenal gland hyperplasia ii
    n1=en:leucinosis | n2=en:adrenal gland hyperplasia ii | rel=r_associated | relid=0 | w=38
  320. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:allanson pantzar mcleod syndrome
    n1=en:leucinosis | n2=en:allanson pantzar mcleod syndrome | rel=r_associated | relid=0 | w=38
  321. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:allgrove syndrome
    n1=en:leucinosis | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=38
  322. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:alpha-1 antitrypsin deficiency
    n1=en:leucinosis | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=38
  323. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:alpha, alpha-trehalase deficiency
    n1=en:leucinosis | n2=en:alpha, alpha-trehalase deficiency | rel=r_associated | relid=0 | w=38
  324. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:amino acid deficiency
    n1=en:leucinosis | n2=en:amino acid deficiency | rel=r_associated | relid=0 | w=38
  325. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:androgen insensitivity syndrome
    n1=en:leucinosis | n2=en:androgen insensitivity syndrome | rel=r_associated | relid=0 | w=38
  326. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:anencephaly
    n1=en:leucinosis | n2=en:anencephaly | rel=r_associated | relid=0 | w=38
  327. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:aortic coarctation
    n1=en:leucinosis | n2=en:aortic coarctation | rel=r_associated | relid=0 | w=38
  328. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:aprosencephaly
    n1=en:leucinosis | n2=en:aprosencephaly | rel=r_associated | relid=0 | w=38
  329. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:atrophic muscular disorder
    n1=en:leucinosis | n2=en:atrophic muscular disorder | rel=r_associated | relid=0 | w=38
  330. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:autosomal dominant optic atrophy
    n1=en:leucinosis | n2=en:autosomal dominant optic atrophy | rel=r_associated | relid=0 | w=38
  331. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:autosomal recessive hypohidrotic ectodermal dysplasia
    n1=en:leucinosis | n2=en:autosomal recessive hypohidrotic ectodermal dysplasia | rel=r_associated | relid=0 | w=38
  332. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:birt-hogg-dube syndrome
    n1=en:leucinosis | n2=en:birt-hogg-dube syndrome | rel=r_associated | relid=0 | w=38
  333. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:blepharophimosis syndrome ohdo type
    n1=en:leucinosis | n2=en:blepharophimosis syndrome ohdo type | rel=r_associated | relid=0 | w=38
  334. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:brown-sequard syndrome
    n1=en:leucinosis | n2=en:brown-sequard syndrome | rel=r_associated | relid=0 | w=38
  335. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:cerebellar ataxia, cayman type
    n1=en:leucinosis | n2=en:cerebellar ataxia, cayman type | rel=r_associated | relid=0 | w=38
  336. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:cerebrotendinous xanthomatosis
    n1=en:leucinosis | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=38
  337. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:childhood myocerebrohepatopathy spectrum
    n1=en:leucinosis | n2=en:childhood myocerebrohepatopathy spectrum | rel=r_associated | relid=0 | w=38
  338. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:classical maple syrup urine disease
    n1=en:leucinosis | n2=en:classical maple syrup urine disease | rel=r_associated | relid=0 | w=38
  339. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:coffin-lowry syndrome
    n1=en:leucinosis | n2=en:coffin-lowry syndrome | rel=r_associated | relid=0 | w=38
  340. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:complication aspects
    n1=en:leucinosis | n2=en:complication aspects | rel=r_associated | relid=0 | w=38
  341. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:congenital
    n1=en:leucinosis | n2=en:congenital | rel=r_associated | relid=0 | w=38
  342. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:congenital alpha-2-antiplasmin deficiency
    n1=en:leucinosis | n2=en:congenital alpha-2-antiplasmin deficiency | rel=r_associated | relid=0 | w=38
  343. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:congenital cataracts, facial dysmorphism, and neuropathy
    n1=en:leucinosis | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=38
  344. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:congenital disorder of glycosylation type ia
    n1=en:leucinosis | n2=en:congenital disorder of glycosylation type ia | rel=r_associated | relid=0 | w=38
  345. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:congenital metabolic disorder
    n1=en:leucinosis | n2=en:congenital metabolic disorder | rel=r_associated | relid=0 | w=38
  346. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism
    n1=en:leucinosis | n2=en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism | rel=r_associated | relid=0 | w=38
  347. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:congenital structural myopathy
    n1=en:leucinosis | n2=en:congenital structural myopathy | rel=r_associated | relid=0 | w=38
  348. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:craniosynostosis
    n1=en:leucinosis | n2=en:craniosynostosis | rel=r_associated | relid=0 | w=38
  349. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:d-glyceric aciduria
    n1=en:leucinosis | n2=en:d-glyceric aciduria | rel=r_associated | relid=0 | w=38
  350. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:de barsy syndrome
    n1=en:leucinosis | n2=en:de barsy syndrome | rel=r_associated | relid=0 | w=38
  351. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:deafness, progressive, with stapes fixation
    n1=en:leucinosis | n2=en:deafness, progressive, with stapes fixation | rel=r_associated | relid=0 | w=38
  352. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:dextrocardia
    n1=en:leucinosis | n2=en:dextrocardia | rel=r_associated | relid=0 | w=38
  353. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:diffuse cerebral sclerosis of schilder
    n1=en:leucinosis | n2=en:diffuse cerebral sclerosis of schilder | rel=r_associated | relid=0 | w=38
  354. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:disorder of aromatic amino acid metabolism
    n1=en:leucinosis | n2=en:disorder of aromatic amino acid metabolism | rel=r_associated | relid=0 | w=38
  355. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:disorder of histidine metabolism
    n1=en:leucinosis | n2=en:disorder of histidine metabolism | rel=r_associated | relid=0 | w=38
  356. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:drug- and toxin-induced pulmonary arterial hypertension
    n1=en:leucinosis | n2=en:drug- and toxin-induced pulmonary arterial hypertension | rel=r_associated | relid=0 | w=38
  357. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:ear, patella, short stature syndrome
    n1=en:leucinosis | n2=en:ear, patella, short stature syndrome | rel=r_associated | relid=0 | w=38
  358. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:exfoliation syndrome
    n1=en:leucinosis | n2=en:exfoliation syndrome | rel=r_associated | relid=0 | w=38
  359. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:factor v and factor viii, combined deficiency of
    n1=en:leucinosis | n2=en:factor v and factor viii, combined deficiency of | rel=r_associated | relid=0 | w=38
  360. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:factor v leiden
    n1=en:leucinosis | n2=en:factor v leiden | rel=r_associated | relid=0 | w=38
  361. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:familial hemorrhagic diathesis
    n1=en:leucinosis | n2=en:familial hemorrhagic diathesis | rel=r_associated | relid=0 | w=38
  362. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:familial hodgkin lymphoma
    n1=en:leucinosis | n2=en:familial hodgkin lymphoma | rel=r_associated | relid=0 | w=38
  363. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:familial hypocalciuric hypercalcemia
    n1=en:leucinosis | n2=en:familial hypocalciuric hypercalcemia | rel=r_associated | relid=0 | w=38
  364. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:fatty acid hydroxylase-associated neurodegeneration
    n1=en:leucinosis | n2=en:fatty acid hydroxylase-associated neurodegeneration | rel=r_associated | relid=0 | w=38
  365. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:focal dermal hypoplasia
    n1=en:leucinosis | n2=en:focal dermal hypoplasia | rel=r_associated | relid=0 | w=38
  366. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:fryns macrocephaly
    n1=en:leucinosis | n2=en:fryns macrocephaly | rel=r_associated | relid=0 | w=38
  367. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:gerstmann-straussler-scheinker disease
    n1=en:leucinosis | n2=en:gerstmann-straussler-scheinker disease | rel=r_associated | relid=0 | w=38
  368. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:glycine dehydrogenase (decarboxylating) deficiency
    n1=en:leucinosis | n2=en:glycine dehydrogenase (decarboxylating) deficiency | rel=r_associated | relid=0 | w=38
  369. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hard skin syndrome parana type
    n1=en:leucinosis | n2=en:hard skin syndrome parana type | rel=r_associated | relid=0 | w=38
  370. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hemophilia a
    n1=en:leucinosis | n2=en:hemophilia a | rel=r_associated | relid=0 | w=38
  371. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hereditary coagulation factor deficiency
    n1=en:leucinosis | n2=en:hereditary coagulation factor deficiency | rel=r_associated | relid=0 | w=38
  372. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hereditary connective tissue disorder
    n1=en:leucinosis | n2=en:hereditary connective tissue disorder | rel=r_associated | relid=0 | w=38
  373. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hereditary disease in family possibly affecting fetus, affecting management of mother
    n1=en:leucinosis | n2=en:hereditary disease in family possibly affecting fetus, affecting management of mother | rel=r_associated | relid=0 | w=38
  374. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hereditary factor xii deficiency disease
    n1=en:leucinosis | n2=en:hereditary factor xii deficiency disease | rel=r_associated | relid=0 | w=38
  375. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hereditary hemorrhagic telangiectasia
    n1=en:leucinosis | n2=en:hereditary hemorrhagic telangiectasia | rel=r_associated | relid=0 | w=38
  376. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hereditary mucosal leukokeratosis
    n1=en:leucinosis | n2=en:hereditary mucosal leukokeratosis | rel=r_associated | relid=0 | w=38
  377. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hereditary pancreatic carcinoma
    n1=en:leucinosis | n2=en:hereditary pancreatic carcinoma | rel=r_associated | relid=0 | w=38
  378. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hereditary spastic paralysis, infantile onset ascending
    n1=en:leucinosis | n2=en:hereditary spastic paralysis, infantile onset ascending | rel=r_associated | relid=0 | w=38
  379. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hereditary wilms tumor
    n1=en:leucinosis | n2=en:hereditary wilms tumor | rel=r_associated | relid=0 | w=38
  380. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:heterotaxy syndrome
    n1=en:leucinosis | n2=en:heterotaxy syndrome | rel=r_associated | relid=0 | w=38
  381. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hnsha due to glucose phosphate isomerase deficiency
    n1=en:leucinosis | n2=en:hnsha due to glucose phosphate isomerase deficiency | rel=r_associated | relid=0 | w=38
  382. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hnsha due to hexokinase deficiency
    n1=en:leucinosis | n2=en:hnsha due to hexokinase deficiency | rel=r_associated | relid=0 | w=38
  383. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hnsha due to nadh diaphorase deficiency
    n1=en:leucinosis | n2=en:hnsha due to nadh diaphorase deficiency | rel=r_associated | relid=0 | w=38
  384. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:holmes-adie syndrome
    n1=en:leucinosis | n2=en:holmes-adie syndrome | rel=r_associated | relid=0 | w=38
  385. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hyperprolinemia type 1
    n1=en:leucinosis | n2=en:hyperprolinemia type 1 | rel=r_associated | relid=0 | w=38
  386. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:hypospadias-mental retardation syndrome
    n1=en:leucinosis | n2=en:hypospadias-mental retardation syndrome | rel=r_associated | relid=0 | w=38
  387. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:i-cell disease
    n1=en:leucinosis | n2=en:i-cell disease | rel=r_associated | relid=0 | w=38
  388. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:imperforate anus
    n1=en:leucinosis | n2=en:imperforate anus | rel=r_associated | relid=0 | w=38
  389. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:in cerebrospinal fluid
    n1=en:leucinosis | n2=en:in cerebrospinal fluid | rel=r_associated | relid=0 | w=38
  390. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:inborn errors of porphyrin metabolism
    n1=en:leucinosis | n2=en:inborn errors of porphyrin metabolism | rel=r_associated | relid=0 | w=38
  391. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:inflammatory hereditary disorder
    n1=en:leucinosis | n2=en:inflammatory hereditary disorder | rel=r_associated | relid=0 | w=38
  392. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:inherited disorder of folate metabolism
    n1=en:leucinosis | n2=en:inherited disorder of folate metabolism | rel=r_associated | relid=0 | w=38
  393. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:isolated hypoplasia of the right ventricle
    n1=en:leucinosis | n2=en:isolated hypoplasia of the right ventricle | rel=r_associated | relid=0 | w=38
  394. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:ketonemia
    n1=en:leucinosis | n2=en:ketonemia | rel=r_associated | relid=0 | w=38
  395. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:kleine-levin syndrome
    n1=en:leucinosis | n2=en:kleine-levin syndrome | rel=r_associated | relid=0 | w=38
  396. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:kshv inflammatory cytokine syndrome
    n1=en:leucinosis | n2=en:kshv inflammatory cytokine syndrome | rel=r_associated | relid=0 | w=38
  397. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:laron syndrome
    n1=en:leucinosis | n2=en:laron syndrome | rel=r_associated | relid=0 | w=38
  398. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:lecithin acyltransferase deficiency
    n1=en:leucinosis | n2=en:lecithin acyltransferase deficiency | rel=r_associated | relid=0 | w=38
  399. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:lennox-gastaut syndrome
    n1=en:leucinosis | n2=en:lennox-gastaut syndrome | rel=r_associated | relid=0 | w=38
  400. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:lesch-nyhan syndrome
    n1=en:leucinosis | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=38
  401. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:lipid metabolism disorder
    n1=en:leucinosis | n2=en:lipid metabolism disorder | rel=r_associated | relid=0 | w=38
  402. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:lissencephaly
    n1=en:leucinosis | n2=en:lissencephaly | rel=r_associated | relid=0 | w=38
  403. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:malignant atrophic papulosis
    n1=en:leucinosis | n2=en:malignant atrophic papulosis | rel=r_associated | relid=0 | w=38
  404. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:marshall syndrome
    n1=en:leucinosis | n2=en:marshall syndrome | rel=r_associated | relid=0 | w=38
  405. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:mayer-rokitansky-kuster-hauser syndrome
    n1=en:leucinosis | n2=en:mayer-rokitansky-kuster-hauser syndrome | rel=r_associated | relid=0 | w=38
  406. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:meesmann corneal dystrophy
    n1=en:leucinosis | n2=en:meesmann corneal dystrophy | rel=r_associated | relid=0 | w=38
  407. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:meningeal tuberculosis
    n1=en:leucinosis | n2=en:meningeal tuberculosis | rel=r_associated | relid=0 | w=38
  408. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:mental retardation
    n1=en:leucinosis | n2=en:mental retardation | rel=r_associated | relid=0 | w=38
  409. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:mental retardation, x-linked, snyder-robinson type
    n1=en:leucinosis | n2=en:mental retardation, x-linked, snyder-robinson type | rel=r_associated | relid=0 | w=38
  410. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:methylenetetrahydrofolate reductase gene mutation
    n1=en:leucinosis | n2=en:methylenetetrahydrofolate reductase gene mutation | rel=r_associated | relid=0 | w=38
  411. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:methylmalonic aciduria
    n1=en:leucinosis | n2=en:methylmalonic aciduria | rel=r_associated | relid=0 | w=38
  412. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:methylmalonyl-coenzyme a mutase deficiency
    n1=en:leucinosis | n2=en:methylmalonyl-coenzyme a mutase deficiency | rel=r_associated | relid=0 | w=38
  413. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:mitochondrial trifunctional protein deficiency
    n1=en:leucinosis | n2=en:mitochondrial trifunctional protein deficiency | rel=r_associated | relid=0 | w=38
  414. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:multiple osteochondromas
    n1=en:leucinosis | n2=en:multiple osteochondromas | rel=r_associated | relid=0 | w=38
  415. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:multiple sulfatase deficiency disease
    n1=en:leucinosis | n2=en:multiple sulfatase deficiency disease | rel=r_associated | relid=0 | w=38
  416. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:muscle l-lactate dehydrogenase deficiency
    n1=en:leucinosis | n2=en:muscle l-lactate dehydrogenase deficiency | rel=r_associated | relid=0 | w=38
  417. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:muscular dystrophy
    n1=en:leucinosis | n2=en:muscular dystrophy | rel=r_associated | relid=0 | w=38
  418. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:myelocerebellar disorder
    n1=en:leucinosis | n2=en:myelocerebellar disorder | rel=r_associated | relid=0 | w=38
  419. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:n-acetylglutamate synthase deficiency
    n1=en:leucinosis | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=38
  420. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:nadh cytochrome b5 reductase deficiency
    n1=en:leucinosis | n2=en:nadh cytochrome b5 reductase deficiency | rel=r_associated | relid=0 | w=38
  421. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:nelson syndrome
    n1=en:leucinosis | n2=en:nelson syndrome | rel=r_associated | relid=0 | w=38
  422. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:neonatal progeroid syndrome
    n1=en:leucinosis | n2=en:neonatal progeroid syndrome | rel=r_associated | relid=0 | w=38
  423. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:neural tube defect
    n1=en:leucinosis | n2=en:neural tube defect | rel=r_associated | relid=0 | w=38
  424. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:neuraminidase deficiency
    n1=en:leucinosis | n2=en:neuraminidase deficiency | rel=r_associated | relid=0 | w=38
  425. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:non-hodgkin lymphoma
    n1=en:leucinosis | n2=en:non-hodgkin lymphoma | rel=r_associated | relid=0 | w=38
  426. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:norrie syndrome
    n1=en:leucinosis | n2=en:norrie syndrome | rel=r_associated | relid=0 | w=38
  427. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:north american indian childhood cirrhosis
    n1=en:leucinosis | n2=en:north american indian childhood cirrhosis | rel=r_associated | relid=0 | w=38
  428. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:nutritional mental retardation
    n1=en:leucinosis | n2=en:nutritional mental retardation | rel=r_associated | relid=0 | w=38
  429. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:organic acid metabolism disorder
    n1=en:leucinosis | n2=en:organic acid metabolism disorder | rel=r_associated | relid=0 | w=38
  430. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:pelger-huet anomaly
    n1=en:leucinosis | n2=en:pelger-huet anomaly | rel=r_associated | relid=0 | w=38
  431. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:perniola krajewska carnevale syndrome
    n1=en:leucinosis | n2=en:perniola krajewska carnevale syndrome | rel=r_associated | relid=0 | w=38
  432. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:persistent fetal circulation
    n1=en:leucinosis | n2=en:persistent fetal circulation | rel=r_associated | relid=0 | w=38
  433. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:phenylketonuria ii
    n1=en:leucinosis | n2=en:phenylketonuria ii | rel=r_associated | relid=0 | w=38
  434. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:presentey anomaly
    n1=en:leucinosis | n2=en:presentey anomaly | rel=r_associated | relid=0 | w=38
  435. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:profound intellectual disabilities
    n1=en:leucinosis | n2=en:profound intellectual disabilities | rel=r_associated | relid=0 | w=38
  436. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:prostate cancer, familial
    n1=en:leucinosis | n2=en:prostate cancer, familial | rel=r_associated | relid=0 | w=38
  437. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:pyridoxine dependency syndrome
    n1=en:leucinosis | n2=en:pyridoxine dependency syndrome | rel=r_associated | relid=0 | w=38
  438. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:renal aminoacidurias
    n1=en:leucinosis | n2=en:renal aminoacidurias | rel=r_associated | relid=0 | w=38
  439. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:rieger syndrome type 1
    n1=en:leucinosis | n2=en:rieger syndrome type 1 | rel=r_associated | relid=0 | w=38
  440. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:seckel syndrome
    n1=en:leucinosis | n2=en:seckel syndrome | rel=r_associated | relid=0 | w=38
  441. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:short stature homeobox deficiency
    n1=en:leucinosis | n2=en:short stature homeobox deficiency | rel=r_associated | relid=0 | w=38
  442. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:shy-drager syndrome
    n1=en:leucinosis | n2=en:shy-drager syndrome | rel=r_associated | relid=0 | w=38
  443. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:sinus histiocytosis with massive lymphadenopathy
    n1=en:leucinosis | n2=en:sinus histiocytosis with massive lymphadenopathy | rel=r_associated | relid=0 | w=38
  444. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:smith-magenis syndrome
    n1=en:leucinosis | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=38
  445. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:sotos syndrome
    n1=en:leucinosis | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=38
  446. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:spasmodic torticollis
    n1=en:leucinosis | n2=en:spasmodic torticollis | rel=r_associated | relid=0 | w=38
  447. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:spondyloenchondrodysplasia with immune dysregulation
    n1=en:leucinosis | n2=en:spondyloenchondrodysplasia with immune dysregulation | rel=r_associated | relid=0 | w=38
  448. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:stickler syndrome
    n1=en:leucinosis | n2=en:stickler syndrome | rel=r_associated | relid=0 | w=38
  449. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:sudden unexplained infant death
    n1=en:leucinosis | n2=en:sudden unexplained infant death | rel=r_associated | relid=0 | w=38
  450. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:trichohepatoenteric syndrome
    n1=en:leucinosis | n2=en:trichohepatoenteric syndrome | rel=r_associated | relid=0 | w=38
  451. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:triploidy syndrome
    n1=en:leucinosis | n2=en:triploidy syndrome | rel=r_associated | relid=0 | w=38
  452. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:trisomy 10p
    n1=en:leucinosis | n2=en:trisomy 10p | rel=r_associated | relid=0 | w=38
  453. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:urine odor, maple syrup
    n1=en:leucinosis | n2=en:urine odor, maple syrup | rel=r_associated | relid=0 | w=38
  454. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:use of ultrasonography
    n1=en:leucinosis | n2=en:use of ultrasonography | rel=r_associated | relid=0 | w=38
  455. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:veterinary aspects
    n1=en:leucinosis | n2=en:veterinary aspects | rel=r_associated | relid=0 | w=38
  456. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:vitelliform macular dystrophy
    n1=en:leucinosis | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=38
  457. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:wegener granulomatosis
    n1=en:leucinosis | n2=en:wegener granulomatosis | rel=r_associated | relid=0 | w=38
  458. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:wiskott-aldrich syndrome
    n1=en:leucinosis | n2=en:wiskott-aldrich syndrome | rel=r_associated | relid=0 | w=38
  459. en:leucinosis -- r_associated #0: 38 / 0.731 -> en:x-linked creatine transporter deficiency
    n1=en:leucinosis | n2=en:x-linked creatine transporter deficiency | rel=r_associated | relid=0 | w=38
  460. en:leucinosis -- r_associated #0: 38 / 0.731 -> homocystinurie
    n1=en:leucinosis | n2=homocystinurie | rel=r_associated | relid=0 | w=38
  461. en:leucinosis -- r_associated #0: 38 / 0.731 -> leucinose intermittente
    n1=en:leucinosis | n2=leucinose intermittente | rel=r_associated | relid=0 | w=38
  462. en:leucinosis -- r_associated #0: 37 / 0.712 -> décarboxylase
    n1=en:leucinosis | n2=décarboxylase | rel=r_associated | relid=0 | w=37
  463. en:leucinosis -- r_associated #0: 37 / 0.712 -> déficit en céto-acide décarboxylase
    n1=en:leucinosis | n2=déficit en céto-acide décarboxylase | rel=r_associated | relid=0 | w=37
  464. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:(1) classic severe (onset of symptoms 4 to 7 days of age)
    n1=en:leucinosis | n2=en:(1) classic severe (onset of symptoms 4 to 7 days of age) | rel=r_associated | relid=0 | w=37
  465. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:(2) intermittent
    n1=en:leucinosis | n2=en:(2) intermittent | rel=r_associated | relid=0 | w=37
  466. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:5 alpha steroid reductase 2 deficiency
    n1=en:leucinosis | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=37
  467. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:aagenaes syndrome
    n1=en:leucinosis | n2=en:aagenaes syndrome | rel=r_associated | relid=0 | w=37
  468. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:acrocallosal syndrome
    n1=en:leucinosis | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=37
  469. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:acrocephalosyndactyly
    n1=en:leucinosis | n2=en:acrocephalosyndactyly | rel=r_associated | relid=0 | w=37
  470. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:aicardi syndrome
    n1=en:leucinosis | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=37
  471. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:aldosterone synthase deficiency
    n1=en:leucinosis | n2=en:aldosterone synthase deficiency | rel=r_associated | relid=0 | w=37
  472. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:alpha thalassemia x-linked mental retardation syndrome
    n1=en:leucinosis | n2=en:alpha thalassemia x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=37
  473. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:alpha-fetoprotein deficiency
    n1=en:leucinosis | n2=en:alpha-fetoprotein deficiency | rel=r_associated | relid=0 | w=37
  474. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:analbuminemia
    n1=en:leucinosis | n2=en:analbuminemia | rel=r_associated | relid=0 | w=37
  475. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:arnold-chiari malformation
    n1=en:leucinosis | n2=en:arnold-chiari malformation | rel=r_associated | relid=0 | w=37
  476. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:ataxia with vitamin e deficiency
    n1=en:leucinosis | n2=en:ataxia with vitamin e deficiency | rel=r_associated | relid=0 | w=37
  477. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
    n1=en:leucinosis | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=37
  478. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:ateliotic dwarfism without insulinopenia
    n1=en:leucinosis | n2=en:ateliotic dwarfism without insulinopenia | rel=r_associated | relid=0 | w=37
  479. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:autosomal recessive ichthyosis
    n1=en:leucinosis | n2=en:autosomal recessive ichthyosis | rel=r_associated | relid=0 | w=37
  480. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:autosomal recessive inheritance
    n1=en:leucinosis | n2=en:autosomal recessive inheritance | rel=r_associated | relid=0 | w=37
  481. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:bloom syndrome
    n1=en:leucinosis | n2=en:bloom syndrome | rel=r_associated | relid=0 | w=37
  482. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:borderline mental retardation (i.q. 70-85)
    n1=en:leucinosis | n2=en:borderline mental retardation (i.q. 70-85) | rel=r_associated | relid=0 | w=37
  483. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:carbamoyl-phosphate synthetase i deficiency
    n1=en:leucinosis | n2=en:carbamoyl-phosphate synthetase i deficiency | rel=r_associated | relid=0 | w=37
  484. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism
    n1=en:leucinosis | n2=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=37
  485. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:chromosome disorder
    n1=en:leucinosis | n2=en:chromosome disorder | rel=r_associated | relid=0 | w=37
  486. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:cockayne syndrome
    n1=en:leucinosis | n2=en:cockayne syndrome | rel=r_associated | relid=0 | w=37
  487. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:congenital adrenal hyperplasia
    n1=en:leucinosis | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=37
  488. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:cystathioninuria
    n1=en:leucinosis | n2=en:cystathioninuria | rel=r_associated | relid=0 | w=37
  489. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
    n1=en:leucinosis | n2=en:disorders of branched-chain amino-acid metabolism and fatty-acid metabolism | rel=r_associated | relid=0 | w=37
  490. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:dyskeratosis congenita, autosomal recessive
    n1=en:leucinosis | n2=en:dyskeratosis congenita, autosomal recessive | rel=r_associated | relid=0 | w=37
  491. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:ectodermal dysplasia/ skin fragility syndrome
    n1=en:leucinosis | n2=en:ectodermal dysplasia/ skin fragility syndrome | rel=r_associated | relid=0 | w=37
  492. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:elevated plasma alloisoleucine
    n1=en:leucinosis | n2=en:elevated plasma alloisoleucine | rel=r_associated | relid=0 | w=37
  493. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:elevated plasma branched chain amino acids (leucine, isoleucine, valine)
    n1=en:leucinosis | n2=en:elevated plasma branched chain amino acids (leucine, isoleucine, valine) | rel=r_associated | relid=0 | w=37
  494. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:embryologic
    n1=en:leucinosis | n2=en:embryologic | rel=r_associated | relid=0 | w=37
  495. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:empty sella syndrome
    n1=en:leucinosis | n2=en:empty sella syndrome | rel=r_associated | relid=0 | w=37
  496. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:ethnologic
    n1=en:leucinosis | n2=en:ethnologic | rel=r_associated | relid=0 | w=37
  497. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:etiology aspects
    n1=en:leucinosis | n2=en:etiology aspects | rel=r_associated | relid=0 | w=37
  498. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:familial chordoma
    n1=en:leucinosis | n2=en:familial chordoma | rel=r_associated | relid=0 | w=37
  499. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:folinic acid responsive seizure syndrome
    n1=en:leucinosis | n2=en:folinic acid responsive seizure syndrome | rel=r_associated | relid=0 | w=37
  500. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:fraxe intellectual disability syndrome
    n1=en:leucinosis | n2=en:fraxe intellectual disability syndrome | rel=r_associated | relid=0 | w=37
  501. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:genetic syndrome
    n1=en:leucinosis | n2=en:genetic syndrome | rel=r_associated | relid=0 | w=37
  502. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:glycogen storage disease
    n1=en:leucinosis | n2=en:glycogen storage disease | rel=r_associated | relid=0 | w=37
  503. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:griscelli syndrome type 2
    n1=en:leucinosis | n2=en:griscelli syndrome type 2 | rel=r_associated | relid=0 | w=37
  504. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:hallermann syndrome
    n1=en:leucinosis | n2=en:hallermann syndrome | rel=r_associated | relid=0 | w=37
  505. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:hellp syndrome
    n1=en:leucinosis | n2=en:hellp syndrome | rel=r_associated | relid=0 | w=37
  506. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:hereditary kidney oncocytoma
    n1=en:leucinosis | n2=en:hereditary kidney oncocytoma | rel=r_associated | relid=0 | w=37
  507. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:hereditary palmoplantar keratoderma gamborg nielsen type
    n1=en:leucinosis | n2=en:hereditary palmoplantar keratoderma gamborg nielsen type | rel=r_associated | relid=0 | w=37
  508. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:hereditary papillary renal cell carcinoma
    n1=en:leucinosis | n2=en:hereditary papillary renal cell carcinoma | rel=r_associated | relid=0 | w=37
  509. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:hereditary paraganglioma
    n1=en:leucinosis | n2=en:hereditary paraganglioma | rel=r_associated | relid=0 | w=37
  510. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:hereditary spherocytosis
    n1=en:leucinosis | n2=en:hereditary spherocytosis | rel=r_associated | relid=0 | w=37
  511. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:hereditary thyroglossal duct cysts
    n1=en:leucinosis | n2=en:hereditary thyroglossal duct cysts | rel=r_associated | relid=0 | w=37
  512. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:hnsha due to glutathione reductase deficiency
    n1=en:leucinosis | n2=en:hnsha due to glutathione reductase deficiency | rel=r_associated | relid=0 | w=37
  513. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:huntington's disease
    n1=en:leucinosis | n2=en:huntington's disease | rel=r_associated | relid=0 | w=37
  514. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:hydrops fetalis
    n1=en:leucinosis | n2=en:hydrops fetalis | rel=r_associated | relid=0 | w=37
  515. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:hymenolepiasis
    n1=en:leucinosis | n2=en:hymenolepiasis | rel=r_associated | relid=0 | w=37
  516. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:hypotonia
    n1=en:leucinosis | n2=en:hypotonia | rel=r_associated | relid=0 | w=37
  517. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:idiopathic hypersomnolence
    n1=en:leucinosis | n2=en:idiopathic hypersomnolence | rel=r_associated | relid=0 | w=37
  518. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:immunoglobulin a deficiency 1
    n1=en:leucinosis | n2=en:immunoglobulin a deficiency 1 | rel=r_associated | relid=0 | w=37
  519. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:in inbred old order mennonite population of lancaster county, msud prevalence is 1/176 newborns
    n1=en:leucinosis | n2=en:in inbred old order mennonite population of lancaster county, msud prevalence is 1/176 newborns | rel=r_associated | relid=0 | w=37
  520. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:in urine
    n1=en:leucinosis | n2=en:in urine | rel=r_associated | relid=0 | w=37
  521. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:inborn biological transport disorder
    n1=en:leucinosis | n2=en:inborn biological transport disorder | rel=r_associated | relid=0 | w=37
  522. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:inborn errors of bilirubin metabolism
    n1=en:leucinosis | n2=en:inborn errors of bilirubin metabolism | rel=r_associated | relid=0 | w=37
  523. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:intestinal disaccharidase deficiency
    n1=en:leucinosis | n2=en:intestinal disaccharidase deficiency | rel=r_associated | relid=0 | w=37
  524. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:jackson-weiss syndrome
    n1=en:leucinosis | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=37
  525. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:kaufman-mckusick syndrome
    n1=en:leucinosis | n2=en:kaufman-mckusick syndrome | rel=r_associated | relid=0 | w=37
  526. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:kernicterus
    n1=en:leucinosis | n2=en:kernicterus | rel=r_associated | relid=0 | w=37
  527. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:kniest dysplasia
    n1=en:leucinosis | n2=en:kniest dysplasia | rel=r_associated | relid=0 | w=37
  528. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:landau-kleffner syndrome
    n1=en:leucinosis | n2=en:landau-kleffner syndrome | rel=r_associated | relid=0 | w=37
  529. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:leukotriene c4 synthase deficiency
    n1=en:leucinosis | n2=en:leukotriene c4 synthase deficiency | rel=r_associated | relid=0 | w=37
  530. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:long-chain acyl-coa dehydrogenase deficiency
    n1=en:leucinosis | n2=en:long-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=37
  531. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:lubs x-linked mental retardation syndrome
    n1=en:leucinosis | n2=en:lubs x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=37
  532. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:majeed syndrome
    n1=en:leucinosis | n2=en:majeed syndrome | rel=r_associated | relid=0 | w=37
  533. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:maple syrup urine disease
    n1=en:leucinosis | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=37
  534. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:maple syrup urine disease, type 1b
    n1=en:leucinosis | n2=en:maple syrup urine disease, type 1b | rel=r_associated | relid=0 | w=37
  535. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:marles greenberg persaud syndrome
    n1=en:leucinosis | n2=en:marles greenberg persaud syndrome | rel=r_associated | relid=0 | w=37
  536. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:maroteaux-lamy syndrome
    n1=en:leucinosis | n2=en:maroteaux-lamy syndrome | rel=r_associated | relid=0 | w=37
  537. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:meckel-gruber syndrome
    n1=en:leucinosis | n2=en:meckel-gruber syndrome | rel=r_associated | relid=0 | w=37
  538. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:mehes syndrome
    n1=en:leucinosis | n2=en:mehes syndrome | rel=r_associated | relid=0 | w=37
  539. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:menkes disease
    n1=en:leucinosis | n2=en:menkes disease | rel=r_associated | relid=0 | w=37
  540. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:metacarpal 4-5 fusion
    n1=en:leucinosis | n2=en:metacarpal 4-5 fusion | rel=r_associated | relid=0 | w=37
  541. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:microcephalic primordial dwarfism toriello type
    n1=en:leucinosis | n2=en:microcephalic primordial dwarfism toriello type | rel=r_associated | relid=0 | w=37
  542. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:mosaic variegated aneuploidy
    n1=en:leucinosis | n2=en:mosaic variegated aneuploidy | rel=r_associated | relid=0 | w=37
  543. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:multicentric osteolysis, nodulosis, and arthropathy
    n1=en:leucinosis | n2=en:multicentric osteolysis, nodulosis, and arthropathy | rel=r_associated | relid=0 | w=37
  544. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:multiple acyl-coa dehydrogenase deficiency
    n1=en:leucinosis | n2=en:multiple acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=37
  545. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:multiple endocrine neoplasia type 1
    n1=en:leucinosis | n2=en:multiple endocrine neoplasia type 1 | rel=r_associated | relid=0 | w=37
  546. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:mutagenic disorder
    n1=en:leucinosis | n2=en:mutagenic disorder | rel=r_associated | relid=0 | w=37
  547. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:myoglobinuria, recurrent
    n1=en:leucinosis | n2=en:myoglobinuria, recurrent | rel=r_associated | relid=0 | w=37
  548. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:myopathy with exercise intolerance, swedish type
    n1=en:leucinosis | n2=en:myopathy with exercise intolerance, swedish type | rel=r_associated | relid=0 | w=37
  549. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:northern epilepsy syndrome
    n1=en:leucinosis | n2=en:northern epilepsy syndrome | rel=r_associated | relid=0 | w=37
  550. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:obesity due to melanocortin 4 receptor deficiency
    n1=en:leucinosis | n2=en:obesity due to melanocortin 4 receptor deficiency | rel=r_associated | relid=0 | w=37
  551. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:oculocutaneous albinism type 4
    n1=en:leucinosis | n2=en:oculocutaneous albinism type 4 | rel=r_associated | relid=0 | w=37
  552. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:orofaciodigital syndrome type 6
    n1=en:leucinosis | n2=en:orofaciodigital syndrome type 6 | rel=r_associated | relid=0 | w=37
  553. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:pancreatic trypsinogen deficiency
    n1=en:leucinosis | n2=en:pancreatic trypsinogen deficiency | rel=r_associated | relid=0 | w=37
  554. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:partington x-linked mental retardation syndrome
    n1=en:leucinosis | n2=en:partington x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=37
  555. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:pettigrew syndrome
    n1=en:leucinosis | n2=en:pettigrew syndrome | rel=r_associated | relid=0 | w=37
  556. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:phenylketonuria
    n1=en:leucinosis | n2=en:phenylketonuria | rel=r_associated | relid=0 | w=37
  557. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:phosphoglycerate kinase 1 deficiency
    n1=en:leucinosis | n2=en:phosphoglycerate kinase 1 deficiency | rel=r_associated | relid=0 | w=37
  558. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:polycystic kidney disease
    n1=en:leucinosis | n2=en:polycystic kidney disease | rel=r_associated | relid=0 | w=37
  559. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:primary lymphedema
    n1=en:leucinosis | n2=en:primary lymphedema | rel=r_associated | relid=0 | w=37
  560. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:primary progressive aphasia
    n1=en:leucinosis | n2=en:primary progressive aphasia | rel=r_associated | relid=0 | w=37
  561. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:pseudohypoparathyroidism
    n1=en:leucinosis | n2=en:pseudohypoparathyroidism | rel=r_associated | relid=0 | w=37
  562. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:pyle metaphyseal dysplasia
    n1=en:leucinosis | n2=en:pyle metaphyseal dysplasia | rel=r_associated | relid=0 | w=37
  563. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:pyruvate carboxylase deficiency
    n1=en:leucinosis | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=37
  564. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:radiotherapeutic
    n1=en:leucinosis | n2=en:radiotherapeutic | rel=r_associated | relid=0 | w=37
  565. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:seizure
    n1=en:leucinosis | n2=en:seizure | rel=r_associated | relid=0 | w=37
  566. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
    n1=en:leucinosis | n2=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | rel=r_associated | relid=0 | w=37
  567. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:simpson golabi behmel syndrome type 1
    n1=en:leucinosis | n2=en:simpson golabi behmel syndrome type 1 | rel=r_associated | relid=0 | w=37
  568. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:sjogren-larsson syndrome
    n1=en:leucinosis | n2=en:sjogren-larsson syndrome | rel=r_associated | relid=0 | w=37
  569. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:smith-lemli-opitz syndrome
    n1=en:leucinosis | n2=en:smith-lemli-opitz syndrome | rel=r_associated | relid=0 | w=37
  570. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:sunct syndrome
    n1=en:leucinosis | n2=en:sunct syndrome | rel=r_associated | relid=0 | w=37
  571. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:surfactant protein deficiency
    n1=en:leucinosis | n2=en:surfactant protein deficiency | rel=r_associated | relid=0 | w=37
  572. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:thyroid dysgenesis
    n1=en:leucinosis | n2=en:thyroid dysgenesis | rel=r_associated | relid=0 | w=37
  573. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:tooth and nail syndrome
    n1=en:leucinosis | n2=en:tooth and nail syndrome | rel=r_associated | relid=0 | w=37
  574. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:transposition of great vessels
    n1=en:leucinosis | n2=en:transposition of great vessels | rel=r_associated | relid=0 | w=37
  575. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:uniparental disomy
    n1=en:leucinosis | n2=en:uniparental disomy | rel=r_associated | relid=0 | w=37
  576. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:upper limb defect with eye and ear abnormalities syndrome
    n1=en:leucinosis | n2=en:upper limb defect with eye and ear abnormalities syndrome | rel=r_associated | relid=0 | w=37
  577. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:usher syndrome
    n1=en:leucinosis | n2=en:usher syndrome | rel=r_associated | relid=0 | w=37
  578. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:uv-sensitive syndrome
    n1=en:leucinosis | n2=en:uv-sensitive syndrome | rel=r_associated | relid=0 | w=37
  579. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:walker-warburg syndrome
    n1=en:leucinosis | n2=en:walker-warburg syndrome | rel=r_associated | relid=0 | w=37
  580. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:wolf-hirschhorn syndrome
    n1=en:leucinosis | n2=en:wolf-hirschhorn syndrome | rel=r_associated | relid=0 | w=37
  581. en:leucinosis -- r_associated #0: 37 / 0.712 -> en:xxxy and xxxxy syndrome
    n1=en:leucinosis | n2=en:xxxy and xxxxy syndrome | rel=r_associated | relid=0 | w=37
  582. en:leucinosis -- r_associated #0: 37 / 0.712 -> érable
    n1=en:leucinosis | n2=érable | rel=r_associated | relid=0 | w=37
  583. en:leucinosis -- r_associated #0: 37 / 0.712 -> Hartnup (maladie de)
    n1=en:leucinosis | n2=Hartnup (maladie de) | rel=r_associated | relid=0 | w=37
  584. en:leucinosis -- r_associated #0: 37 / 0.712 -> hyperleucinémie
    n1=en:leucinosis | n2=hyperleucinémie | rel=r_associated | relid=0 | w=37
  585. en:leucinosis -- r_associated #0: 37 / 0.712 -> maladie
    n1=en:leucinosis | n2=maladie | rel=r_associated | relid=0 | w=37
  586. en:leucinosis -- r_associated #0: 37 / 0.712 -> maladie des urines à odeur de sirop d'érable
    n1=en:leucinosis | n2=maladie des urines à odeur de sirop d'érable | rel=r_associated | relid=0 | w=37
  587. en:leucinosis -- r_associated #0: 37 / 0.712 -> maladies
    n1=en:leucinosis | n2=maladies | rel=r_associated | relid=0 | w=37
  588. en:leucinosis -- r_associated #0: 37 / 0.712 -> médecine
    (science)
    n1=en:leucinosis | n2=médecine
    (science)
    | rel=r_associated | relid=0 | w=37
  589. en:leucinosis -- r_associated #0: 37 / 0.712 -> urine
    n1=en:leucinosis | n2=urine | rel=r_associated | relid=0 | w=37
  590. en:leucinosis -- r_associated #0: 36 / 0.692 -> biochimie
    n1=en:leucinosis | n2=biochimie | rel=r_associated | relid=0 | w=36
  591. en:leucinosis -- r_associated #0: 36 / 0.692 -> cétoacidurie ramifiée
    n1=en:leucinosis | n2=cétoacidurie ramifiée | rel=r_associated | relid=0 | w=36
  592. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:17 alpha-hydroxyprogesterone aldolase deficiency
    n1=en:leucinosis | n2=en:17 alpha-hydroxyprogesterone aldolase deficiency | rel=r_associated | relid=0 | w=36
  593. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:21-hydroxylase deficiency
    n1=en:leucinosis | n2=en:21-hydroxylase deficiency | rel=r_associated | relid=0 | w=36
  594. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:acquired hyperostosis syndrome
    n1=en:leucinosis | n2=en:acquired hyperostosis syndrome | rel=r_associated | relid=0 | w=36
  595. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:afibrinogenemia
    n1=en:leucinosis | n2=en:afibrinogenemia | rel=r_associated | relid=0 | w=36
  596. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:ainhum
    n1=en:leucinosis | n2=en:ainhum | rel=r_associated | relid=0 | w=36
  597. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:alkaptonuria
    n1=en:leucinosis | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=36
  598. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:allan-herndon-dudley syndrome
    n1=en:leucinosis | n2=en:allan-herndon-dudley syndrome | rel=r_associated | relid=0 | w=36
  599. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:amino acid transport disorder
    n1=en:leucinosis | n2=en:amino acid transport disorder | rel=r_associated | relid=0 | w=36
  600. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:aminoaciduria
    n1=en:leucinosis | n2=en:aminoaciduria | rel=r_associated | relid=0 | w=36
  601. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:arginine:glycine amidinotransferase deficiency
    n1=en:leucinosis | n2=en:arginine:glycine amidinotransferase deficiency | rel=r_associated | relid=0 | w=36
  602. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:autoinflammation, lipodystrophy and dermatosis syndrome
    n1=en:leucinosis | n2=en:autoinflammation, lipodystrophy and dermatosis syndrome | rel=r_associated | relid=0 | w=36
  603. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:autosomal recessive distal osteolysis syndrome
    n1=en:leucinosis | n2=en:autosomal recessive distal osteolysis syndrome | rel=r_associated | relid=0 | w=36
  604. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:biotinidase deficiency
    n1=en:leucinosis | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=36
  605. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:borjeson-forssman-lehmann syndrome
    n1=en:leucinosis | n2=en:borjeson-forssman-lehmann syndrome | rel=r_associated | relid=0 | w=36
  606. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:branched chain ketoaciduria (alpha-keto isocaproate, alpha-keto-beta methylisovalerate, alpha-keto isovalerate)
    n1=en:leucinosis | n2=en:branched chain ketoaciduria (alpha-keto isocaproate, alpha-keto-beta methylisovalerate, alpha-keto isovalerate) | rel=r_associated | relid=0 | w=36
  607. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:brown-vialetto-van laere syndrome
    n1=en:leucinosis | n2=en:brown-vialetto-van laere syndrome | rel=r_associated | relid=0 | w=36
  608. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:cancer genetics
    n1=en:leucinosis | n2=en:cancer genetics | rel=r_associated | relid=0 | w=36
  609. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:carbohydrate metabolism, inborn errors
    n1=en:leucinosis | n2=en:carbohydrate metabolism, inborn errors | rel=r_associated | relid=0 | w=36
  610. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:carnitine palmitoyltransferase ii deficiency
    n1=en:leucinosis | n2=en:carnitine palmitoyltransferase ii deficiency | rel=r_associated | relid=0 | w=36
  611. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:cat-eye syndrome
    n1=en:leucinosis | n2=en:cat-eye syndrome | rel=r_associated | relid=0 | w=36
  612. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:cerebrooculofacioskeletal syndrome
    n1=en:leucinosis | n2=en:cerebrooculofacioskeletal syndrome | rel=r_associated | relid=0 | w=36
  613. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:cleidocranial dysplasia
    n1=en:leucinosis | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=36
  614. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:combined lipase deficiency
    n1=en:leucinosis | n2=en:combined lipase deficiency | rel=r_associated | relid=0 | w=36
  615. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:congenital bowing of long bone
    n1=en:leucinosis | n2=en:congenital bowing of long bone | rel=r_associated | relid=0 | w=36
  616. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:congenital leptin deficiency
    n1=en:leucinosis | n2=en:congenital leptin deficiency | rel=r_associated | relid=0 | w=36
  617. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:congenital myasthenic syndrome
    n1=en:leucinosis | n2=en:congenital myasthenic syndrome | rel=r_associated | relid=0 | w=36
  618. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:congenital pain insensitivity
    n1=en:leucinosis | n2=en:congenital pain insensitivity | rel=r_associated | relid=0 | w=36
  619. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:cor triatriatum
    n1=en:leucinosis | n2=en:cor triatriatum | rel=r_associated | relid=0 | w=36
  620. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:cowden syndrome
    n1=en:leucinosis | n2=en:cowden syndrome | rel=r_associated | relid=0 | w=36
  621. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:cryopyrin-associated periodic syndrome
    n1=en:leucinosis | n2=en:cryopyrin-associated periodic syndrome | rel=r_associated | relid=0 | w=36
  622. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:cystinosis
    n1=en:leucinosis | n2=en:cystinosis | rel=r_associated | relid=0 | w=36
  623. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:death in untreated children
    n1=en:leucinosis | n2=en:death in untreated children | rel=r_associated | relid=0 | w=36
  624. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:deletion 18p syndrome
    n1=en:leucinosis | n2=en:deletion 18p syndrome | rel=r_associated | relid=0 | w=36
  625. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:disorder due to cytochrome p450 enzyme variant
    n1=en:leucinosis | n2=en:disorder due to cytochrome p450 enzyme variant | rel=r_associated | relid=0 | w=36
  626. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:disorder of branched-chain amino acid metabolism
    n1=en:leucinosis | n2=en:disorder of branched-chain amino acid metabolism | rel=r_associated | relid=0 | w=36
  627. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:disorder of glycosaminoglycan metabolism
    n1=en:leucinosis | n2=en:disorder of glycosaminoglycan metabolism | rel=r_associated | relid=0 | w=36
  628. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:disorder of lysine and hydroxylysine metabolism
    n1=en:leucinosis | n2=en:disorder of lysine and hydroxylysine metabolism | rel=r_associated | relid=0 | w=36
  629. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:donnai-barrow syndrome
    n1=en:leucinosis | n2=en:donnai-barrow syndrome | rel=r_associated | relid=0 | w=36
  630. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:down syndrome
    n1=en:leucinosis | n2=en:down syndrome | rel=r_associated | relid=0 | w=36
  631. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome
    n1=en:leucinosis | n2=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | rel=r_associated | relid=0 | w=36
  632. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:ectromelia
    n1=en:leucinosis | n2=en:ectromelia | rel=r_associated | relid=0 | w=36
  633. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:ehlers-danlos syndrome, type vi
    n1=en:leucinosis | n2=en:ehlers-danlos syndrome, type vi | rel=r_associated | relid=0 | w=36
  634. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:epiphyseal dysplasia, multiple, 4
    n1=en:leucinosis | n2=en:epiphyseal dysplasia, multiple, 4 | rel=r_associated | relid=0 | w=36
  635. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:erythropoietic porphyria
    n1=en:leucinosis | n2=en:erythropoietic porphyria | rel=r_associated | relid=0 | w=36
  636. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:familial dysautonomia
    n1=en:leucinosis | n2=en:familial dysautonomia | rel=r_associated | relid=0 | w=36
  637. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:familial erythrocytosis due to diphosphoglycerate mutase deficiency
    n1=en:leucinosis | n2=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=36
  638. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:fanconi anemia
    n1=en:leucinosis | n2=en:fanconi anemia | rel=r_associated | relid=0 | w=36
  639. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:female restricted epilepsy with intellectual disability syndrome
    n1=en:leucinosis | n2=en:female restricted epilepsy with intellectual disability syndrome | rel=r_associated | relid=0 | w=36
  640. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:fetal akinesia deformation sequence
    n1=en:leucinosis | n2=en:fetal akinesia deformation sequence | rel=r_associated | relid=0 | w=36
  641. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:fuchs endothelial dystrophy
    n1=en:leucinosis | n2=en:fuchs endothelial dystrophy | rel=r_associated | relid=0 | w=36
  642. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:fucosidosis
    n1=en:leucinosis | n2=en:fucosidosis | rel=r_associated | relid=0 | w=36
  643. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:gaze palsy, familial horizontal, with progressive scoliosis
    n1=en:leucinosis | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=36
  644. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:geroderma osteodysplastica
    n1=en:leucinosis | n2=en:geroderma osteodysplastica | rel=r_associated | relid=0 | w=36
  645. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:glutamate-cysteine ligase deficiency
    n1=en:leucinosis | n2=en:glutamate-cysteine ligase deficiency | rel=r_associated | relid=0 | w=36
  646. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:glycine encephalopathy
    n1=en:leucinosis | n2=en:glycine encephalopathy | rel=r_associated | relid=0 | w=36
  647. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:gurrieri sammito bellussi syndrome
    n1=en:leucinosis | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=36
  648. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:hereditary angioedema
    n1=en:leucinosis | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=36
  649. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:hereditary breast/ovarian cancer - brca1
    n1=en:leucinosis | n2=en:hereditary breast/ovarian cancer - brca1 | rel=r_associated | relid=0 | w=36
  650. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:hereditary disease in family possibly affecting fetus
    n1=en:leucinosis | n2=en:hereditary disease in family possibly affecting fetus | rel=r_associated | relid=0 | w=36
  651. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:hereditary disease in family possibly affecting fetus, affecting management of mother, with delivery
    n1=en:leucinosis | n2=en:hereditary disease in family possibly affecting fetus, affecting management of mother, with delivery | rel=r_associated | relid=0 | w=36
  652. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:hereditary dysplasminogenemia
    n1=en:leucinosis | n2=en:hereditary dysplasminogenemia | rel=r_associated | relid=0 | w=36
  653. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:hereditary factor xi deficiency disease
    n1=en:leucinosis | n2=en:hereditary factor xi deficiency disease | rel=r_associated | relid=0 | w=36
  654. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:hereditary melanoma
    n1=en:leucinosis | n2=en:hereditary melanoma | rel=r_associated | relid=0 | w=36
  655. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:histidinemia
    n1=en:leucinosis | n2=en:histidinemia | rel=r_associated | relid=0 | w=36
  656. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:hnsha due to aldolase a deficiency
    n1=en:leucinosis | n2=en:hnsha due to aldolase a deficiency | rel=r_associated | relid=0 | w=36
  657. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:hyperimmunoglobulin syndrome
    n1=en:leucinosis | n2=en:hyperimmunoglobulin syndrome | rel=r_associated | relid=0 | w=36
  658. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:hypermethioniuria
    n1=en:leucinosis | n2=en:hypermethioniuria | rel=r_associated | relid=0 | w=36
  659. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
    n1=en:leucinosis | n2=en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | rel=r_associated | relid=0 | w=36
  660. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:imperforate vagina
    n1=en:leucinosis | n2=en:imperforate vagina | rel=r_associated | relid=0 | w=36
  661. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:inborn errors of carbohydrate metabolism (excl glucose)
    n1=en:leucinosis | n2=en:inborn errors of carbohydrate metabolism (excl glucose) | rel=r_associated | relid=0 | w=36
  662. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:intermediate maple syrup urine disease
    n1=en:leucinosis | n2=en:intermediate maple syrup urine disease | rel=r_associated | relid=0 | w=36
  663. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:jeune syndrome
    n1=en:leucinosis | n2=en:jeune syndrome | rel=r_associated | relid=0 | w=36
  664. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:kabuki syndrome
    n1=en:leucinosis | n2=en:kabuki syndrome | rel=r_associated | relid=0 | w=36
  665. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:kartagener syndrome
    n1=en:leucinosis | n2=en:kartagener syndrome | rel=r_associated | relid=0 | w=36
  666. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:kohlschutter tonz syndrome
    n1=en:leucinosis | n2=en:kohlschutter tonz syndrome | rel=r_associated | relid=0 | w=36
  667. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:leprosy
    n1=en:leucinosis | n2=en:leprosy | rel=r_associated | relid=0 | w=36
  668. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:leri-weill dyschondrosteosis
    n1=en:leucinosis | n2=en:leri-weill dyschondrosteosis | rel=r_associated | relid=0 | w=36
  669. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:lethal congenital contracture syndrome 2
    n1=en:leucinosis | n2=en:lethal congenital contracture syndrome 2 | rel=r_associated | relid=0 | w=36
  670. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:lipoid proteinosis of urbach and wiethe
    n1=en:leucinosis | n2=en:lipoid proteinosis of urbach and wiethe | rel=r_associated | relid=0 | w=36
  671. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:mandibuloacral dysplasia with type a lipodystrophy
    n1=en:leucinosis | n2=en:mandibuloacral dysplasia with type a lipodystrophy | rel=r_associated | relid=0 | w=36
  672. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:mannosidosis
    n1=en:leucinosis | n2=en:mannosidosis | rel=r_associated | relid=0 | w=36
  673. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:marfan syndrome
    n1=en:leucinosis | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=36
  674. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:methylene thf reductase deficiency and homocystinuria
    n1=en:leucinosis | n2=en:methylene thf reductase deficiency and homocystinuria | rel=r_associated | relid=0 | w=36
  675. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:microcephaly deafness syndrome
    n1=en:leucinosis | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=36
  676. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:mitochondrial neurogastrointestingal encephalopathy
    n1=en:leucinosis | n2=en:mitochondrial neurogastrointestingal encephalopathy | rel=r_associated | relid=0 | w=36
  677. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:mowat-wilson syndrome
    n1=en:leucinosis | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=36
  678. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:mutyh-associated polyposis
    n1=en:leucinosis | n2=en:mutyh-associated polyposis | rel=r_associated | relid=0 | w=36
  679. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:myokymia
    n1=en:leucinosis | n2=en:myokymia | rel=r_associated | relid=0 | w=36
  680. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:myositis
    n1=en:leucinosis | n2=en:myositis | rel=r_associated | relid=0 | w=36
  681. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:nail-patella syndrome
    n1=en:leucinosis | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=36
  682. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:neuroacanthocytosis
    n1=en:leucinosis | n2=en:neuroacanthocytosis | rel=r_associated | relid=0 | w=36
  683. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:neurofibromatosis type 2
    n1=en:leucinosis | n2=en:neurofibromatosis type 2 | rel=r_associated | relid=0 | w=36
  684. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:newborn conditions with positive markers:prid:pt:bld.dot:nom
    n1=en:leucinosis | n2=en:newborn conditions with positive markers:prid:pt:bld.dot:nom | rel=r_associated | relid=0 | w=36
  685. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:nijmegen breakage syndrome
    n1=en:leucinosis | n2=en:nijmegen breakage syndrome | rel=r_associated | relid=0 | w=36
  686. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:odontohypophosphatasia (disorder)
    n1=en:leucinosis | n2=en:odontohypophosphatasia (disorder) | rel=r_associated | relid=0 | w=36
  687. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:other disorders of aromatic amino-acid metabolism
    n1=en:leucinosis | n2=en:other disorders of aromatic amino-acid metabolism | rel=r_associated | relid=0 | w=36
  688. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:otopalatodigital syndrome type 1
    n1=en:leucinosis | n2=en:otopalatodigital syndrome type 1 | rel=r_associated | relid=0 | w=36
  689. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:pain agnosia
    n1=en:leucinosis | n2=en:pain agnosia | rel=r_associated | relid=0 | w=36
  690. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:pantothenate kinase-associated neurodegeneration
    n1=en:leucinosis | n2=en:pantothenate kinase-associated neurodegeneration | rel=r_associated | relid=0 | w=36
  691. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:pediatric terminology
    n1=en:leucinosis | n2=en:pediatric terminology | rel=r_associated | relid=0 | w=36
  692. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:pemphigoid gestationis
    n1=en:leucinosis | n2=en:pemphigoid gestationis | rel=r_associated | relid=0 | w=36
  693. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:pentalogy of cantrell
    n1=en:leucinosis | n2=en:pentalogy of cantrell | rel=r_associated | relid=0 | w=36
  694. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:peritoneal panniculitis
    n1=en:leucinosis | n2=en:peritoneal panniculitis | rel=r_associated | relid=0 | w=36
  695. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:phosphoenolpyruvate carboxykinase deficiency
    n1=en:leucinosis | n2=en:phosphoenolpyruvate carboxykinase deficiency | rel=r_associated | relid=0 | w=36
  696. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:positive urine dnph screening test
    n1=en:leucinosis | n2=en:positive urine dnph screening test | rel=r_associated | relid=0 | w=36
  697. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:progressive bulbar palsy
    n1=en:leucinosis | n2=en:progressive bulbar palsy | rel=r_associated | relid=0 | w=36
  698. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:psychology qualifier
    n1=en:leucinosis | n2=en:psychology qualifier | rel=r_associated | relid=0 | w=36
  699. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:radial aplasia-thrombocytopenia syndrome
    n1=en:leucinosis | n2=en:radial aplasia-thrombocytopenia syndrome | rel=r_associated | relid=0 | w=36
  700. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:rna polymerase iii-related leukodystrophy
    n1=en:leucinosis | n2=en:rna polymerase iii-related leukodystrophy | rel=r_associated | relid=0 | w=36
  701. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:sex chromosome disorders
    n1=en:leucinosis | n2=en:sex chromosome disorders | rel=r_associated | relid=0 | w=36
  702. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:spastic ataxia, charlevoix-saguenay type
    n1=en:leucinosis | n2=en:spastic ataxia, charlevoix-saguenay type | rel=r_associated | relid=0 | w=36
  703. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:spondylocarpotarsal synostosis syndrome
    n1=en:leucinosis | n2=en:spondylocarpotarsal synostosis syndrome | rel=r_associated | relid=0 | w=36
  704. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:stiff skin syndrome
    n1=en:leucinosis | n2=en:stiff skin syndrome | rel=r_associated | relid=0 | w=36
  705. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:syndrome of apparent mineralocorticoid excess
    n1=en:leucinosis | n2=en:syndrome of apparent mineralocorticoid excess | rel=r_associated | relid=0 | w=36
  706. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:takotsubo cardiomyopathy
    n1=en:leucinosis | n2=en:takotsubo cardiomyopathy | rel=r_associated | relid=0 | w=36
  707. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:tay-sachs disease
    n1=en:leucinosis | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=36
  708. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:thanatophoric dysplasia
    n1=en:leucinosis | n2=en:thanatophoric dysplasia | rel=r_associated | relid=0 | w=36
  709. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:tiglic acidemia
    n1=en:leucinosis | n2=en:tiglic acidemia | rel=r_associated | relid=0 | w=36
  710. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:togaviridae infection
    n1=en:leucinosis | n2=en:togaviridae infection | rel=r_associated | relid=0 | w=36
  711. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:trichothiodystrophy
    n1=en:leucinosis | n2=en:trichothiodystrophy | rel=r_associated | relid=0 | w=36
  712. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:unspecified mental retardation; without mention of impairment of behaviour
    n1=en:leucinosis | n2=en:unspecified mental retardation; without mention of impairment of behaviour | rel=r_associated | relid=0 | w=36
  713. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:uveomeningoencephalitic syndrome
    n1=en:leucinosis | n2=en:uveomeningoencephalitic syndrome | rel=r_associated | relid=0 | w=36
  714. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:very long-chain acyl-coa dehydrogenase deficiency
    n1=en:leucinosis | n2=en:very long-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=36
  715. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:von willebrand disease
    n1=en:leucinosis | n2=en:von willebrand disease | rel=r_associated | relid=0 | w=36
  716. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:wallerian degeneration
    n1=en:leucinosis | n2=en:wallerian degeneration | rel=r_associated | relid=0 | w=36
  717. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:weaver syndrome
    n1=en:leucinosis | n2=en:weaver syndrome | rel=r_associated | relid=0 | w=36
  718. en:leucinosis -- r_associated #0: 36 / 0.692 -> en:wilms tumor
    n1=en:leucinosis | n2=en:wilms tumor | rel=r_associated | relid=0 | w=36
  719. en:leucinosis -- r_associated #0: 36 / 0.692 -> handicap
    n1=en:leucinosis | n2=handicap | rel=r_associated | relid=0 | w=36
  720. en:leucinosis -- r_associated #0: 36 / 0.692 -> isoleucine
    n1=en:leucinosis | n2=isoleucine | rel=r_associated | relid=0 | w=36
  721. en:leucinosis -- r_associated #0: 36 / 0.692 -> leucinose aiguë
    n1=en:leucinosis | n2=leucinose aiguë | rel=r_associated | relid=0 | w=36
  722. en:leucinosis -- r_associated #0: 36 / 0.692 -> leucinose intermédiaire
    n1=en:leucinosis | n2=leucinose intermédiaire | rel=r_associated | relid=0 | w=36
  723. en:leucinosis -- r_associated #0: 36 / 0.692 -> leucinoses
    n1=en:leucinosis | n2=leucinoses | rel=r_associated | relid=0 | w=36
  724. en:leucinosis -- r_associated #0: 36 / 0.692 -> maladie génétique congénitale
    n1=en:leucinosis | n2=maladie génétique congénitale | rel=r_associated | relid=0 | w=36
  725. en:leucinosis -- r_associated #0: 36 / 0.692 -> maladie génétique du métabolisme des acides aminés
    n1=en:leucinosis | n2=maladie génétique du métabolisme des acides aminés | rel=r_associated | relid=0 | w=36
  726. en:leucinosis -- r_associated #0: 36 / 0.692 -> maladies du sirop d'erable
    n1=en:leucinosis | n2=maladies du sirop d'erable | rel=r_associated | relid=0 | w=36
  727. en:leucinosis -- r_associated #0: 36 / 0.692 -> opisthotonos
    n1=en:leucinosis | n2=opisthotonos | rel=r_associated | relid=0 | w=36
  728. en:leucinosis -- r_associated #0: 36 / 0.692 -> syndrome de Hartnup
    n1=en:leucinosis | n2=syndrome de Hartnup | rel=r_associated | relid=0 | w=36
  729. en:leucinosis -- r_associated #0: 36 / 0.692 -> valine
    n1=en:leucinosis | n2=valine | rel=r_associated | relid=0 | w=36
  730. en:leucinosis -- r_associated #0: 35 / 0.673 -> cérumen
    n1=en:leucinosis | n2=cérumen | rel=r_associated | relid=0 | w=35
  731. en:leucinosis -- r_associated #0: 35 / 0.673 -> cerveau
    n1=en:leucinosis | n2=cerveau | rel=r_associated | relid=0 | w=35
  732. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:ataxia
    n1=en:leucinosis | n2=en:ataxia | rel=r_associated | relid=0 | w=35
  733. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:cask related intellectual disability
    n1=en:leucinosis | n2=en:cask related intellectual disability | rel=r_associated | relid=0 | w=35
  734. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:circulating enzyme deficiency
    n1=en:leucinosis | n2=en:circulating enzyme deficiency | rel=r_associated | relid=0 | w=35
  735. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:congenital amegakaryocytic thrombocytopenia
    n1=en:leucinosis | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=35
  736. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:familial adenomatous polyposis
    n1=en:leucinosis | n2=en:familial adenomatous polyposis | rel=r_associated | relid=0 | w=35
  737. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:in blood
    n1=en:leucinosis | n2=en:in blood | rel=r_associated | relid=0 | w=35
  738. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:inborn lipid/lipoprotein disorder
    n1=en:leucinosis | n2=en:inborn lipid/lipoprotein disorder | rel=r_associated | relid=0 | w=35
  739. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:intermittent branched-chain ketonuria
    n1=en:leucinosis | n2=en:intermittent branched-chain ketonuria | rel=r_associated | relid=0 | w=35
  740. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:iridocorneal endothelial syndrome
    n1=en:leucinosis | n2=en:iridocorneal endothelial syndrome | rel=r_associated | relid=0 | w=35
  741. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:juvenile polyposis syndrome
    n1=en:leucinosis | n2=en:juvenile polyposis syndrome | rel=r_associated | relid=0 | w=35
  742. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:orotic aciduria
    n1=en:leucinosis | n2=en:orotic aciduria | rel=r_associated | relid=0 | w=35
  743. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:peters-plus syndrome
    n1=en:leucinosis | n2=en:peters-plus syndrome | rel=r_associated | relid=0 | w=35
  744. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:postaxial polydactyly, type b
    n1=en:leucinosis | n2=en:postaxial polydactyly, type b | rel=r_associated | relid=0 | w=35
  745. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:prader-willi syndrome
    n1=en:leucinosis | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=35
  746. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:rhabdoid tumor predisposition syndrome
    n1=en:leucinosis | n2=en:rhabdoid tumor predisposition syndrome | rel=r_associated | relid=0 | w=35
  747. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:schwannomatosis
    n1=en:leucinosis | n2=en:schwannomatosis | rel=r_associated | relid=0 | w=35
  748. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:sitosterolemia
    n1=en:leucinosis | n2=en:sitosterolemia | rel=r_associated | relid=0 | w=35
  749. en:leucinosis -- r_associated #0: 35 / 0.673 -> en:tungland bellman syndrome
    n1=en:leucinosis | n2=en:tungland bellman syndrome | rel=r_associated | relid=0 | w=35
  750. en:leucinosis -- r_associated #0: 34 / 0.654 -> cerveau
    (anatomie)
    n1=en:leucinosis | n2=cerveau
    (anatomie)
    | rel=r_associated | relid=0 | w=34
  751. en:leucinosis -- r_associated #0: 34 / 0.654 -> chromosome
    n1=en:leucinosis | n2=chromosome | rel=r_associated | relid=0 | w=34
  752. en:leucinosis -- r_associated #0: 34 / 0.654 -> chromosome 7
    n1=en:leucinosis | n2=chromosome 7 | rel=r_associated | relid=0 | w=34
  753. en:leucinosis -- r_associated #0: 34 / 0.654 -> déficit en alpha-céto-acide déshydrogénase
    n1=en:leucinosis | n2=déficit en alpha-céto-acide déshydrogénase | rel=r_associated | relid=0 | w=34
  754. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:2-hydroxyglutaric aciduria
    n1=en:leucinosis | n2=en:2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=34
  755. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:3-methyl-2-oxobutanoate dehydrogenase (lipoamide)
    n1=en:leucinosis | n2=en:3-methyl-2-oxobutanoate dehydrogenase (lipoamide) | rel=r_associated | relid=0 | w=34
  756. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:3-methylglutaconic aciduria
    n1=en:leucinosis | n2=en:3-methylglutaconic aciduria | rel=r_associated | relid=0 | w=34
  757. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:5' 10' methylenetetrahydrofolate reductase deficiency
    n1=en:leucinosis | n2=en:5' 10' methylenetetrahydrofolate reductase deficiency | rel=r_associated | relid=0 | w=34
  758. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:achondrogenesis
    n1=en:leucinosis | n2=en:achondrogenesis | rel=r_associated | relid=0 | w=34
  759. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:acid phosphatase deficiency
    n1=en:leucinosis | n2=en:acid phosphatase deficiency | rel=r_associated | relid=0 | w=34
  760. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:albinism
    n1=en:leucinosis | n2=en:albinism | rel=r_associated | relid=0 | w=34
  761. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:amelogenesis imperfecta - recessive - rough
    n1=en:leucinosis | n2=en:amelogenesis imperfecta - recessive - rough | rel=r_associated | relid=0 | w=34
  762. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:amelogenesis imperfecta and gingival hyperplasia syndrome
    n1=en:leucinosis | n2=en:amelogenesis imperfecta and gingival hyperplasia syndrome | rel=r_associated | relid=0 | w=34
  763. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:antithrombin iii deficiency
    n1=en:leucinosis | n2=en:antithrombin iii deficiency | rel=r_associated | relid=0 | w=34
  764. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:arrhythmogenic right ventricular dysplasia
    n1=en:leucinosis | n2=en:arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=34
  765. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:arterial tortuosity syndrome
    n1=en:leucinosis | n2=en:arterial tortuosity syndrome | rel=r_associated | relid=0 | w=34
  766. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:arthrogryposis
    n1=en:leucinosis | n2=en:arthrogryposis | rel=r_associated | relid=0 | w=34
  767. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:arthrogryposis multiplex congenita, neurogenic type (disorder)
    n1=en:leucinosis | n2=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | rel=r_associated | relid=0 | w=34
  768. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:aspects of mortality statistics
    n1=en:leucinosis | n2=en:aspects of mortality statistics | rel=r_associated | relid=0 | w=34
  769. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:autoimmune polyendocrinopathy syndrome
    n1=en:leucinosis | n2=en:autoimmune polyendocrinopathy syndrome | rel=r_associated | relid=0 | w=34
  770. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:autosomal recessive muscular dystrophy with limb girdle distribution
    n1=en:leucinosis | n2=en:autosomal recessive muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=34
  771. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:baller-gerold syndrome
    n1=en:leucinosis | n2=en:baller-gerold syndrome | rel=r_associated | relid=0 | w=34
  772. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:basal ganglia disease, biotin-responsive
    n1=en:leucinosis | n2=en:basal ganglia disease, biotin-responsive | rel=r_associated | relid=0 | w=34
  773. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:bckdha gene
    n1=en:leucinosis | n2=en:bckdha gene | rel=r_associated | relid=0 | w=34
  774. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:beare-stevenson cutis gyrata syndrome
    n1=en:leucinosis | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=34
  775. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:benign mucous membrane pemphigoid
    n1=en:leucinosis | n2=en:benign mucous membrane pemphigoid | rel=r_associated | relid=0 | w=34
  776. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:beta-ketothiolase deficiency
    n1=en:leucinosis | n2=en:beta-ketothiolase deficiency | rel=r_associated | relid=0 | w=34
  777. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:bietti crystalline corneoretinal dystrophy
    n1=en:leucinosis | n2=en:bietti crystalline corneoretinal dystrophy | rel=r_associated | relid=0 | w=34
  778. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:brachydactyly syndrome type b
    n1=en:leucinosis | n2=en:brachydactyly syndrome type b | rel=r_associated | relid=0 | w=34
  779. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:brain mri shows diffusion abnormalities
    n1=en:leucinosis | n2=en:brain mri shows diffusion abnormalities | rel=r_associated | relid=0 | w=34
  780. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:branched-chain ketoaciduria
    n1=en:leucinosis | n2=en:branched-chain ketoaciduria | rel=r_associated | relid=0 | w=34
  781. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:carnitine palmitoyltransferase deficiency
    n1=en:leucinosis | n2=en:carnitine palmitoyltransferase deficiency | rel=r_associated | relid=0 | w=34
  782. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:charcot-marie-tooth disease type 4
    n1=en:leucinosis | n2=en:charcot-marie-tooth disease type 4 | rel=r_associated | relid=0 | w=34
  783. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:chilblains
    n1=en:leucinosis | n2=en:chilblains | rel=r_associated | relid=0 | w=34
  784. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:childhood hypophosphatasia (disorder)
    n1=en:leucinosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  785. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:choroideremia
    n1=en:leucinosis | n2=en:choroideremia | rel=r_associated | relid=0 | w=34
  786. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:chylomicron retention disease
    n1=en:leucinosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  787. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:cohen syndrome
    n1=en:leucinosis | n2=en:cohen syndrome | rel=r_associated | relid=0 | w=34
  788. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:complex regional pain syndrome ii
    n1=en:leucinosis | n2=en:complex regional pain syndrome ii | rel=r_associated | relid=0 | w=34
  789. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:congenital disorder of deglycosylation
    n1=en:leucinosis | n2=en:congenital disorder of deglycosylation | rel=r_associated | relid=0 | w=34
  790. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:congenital disorder of glycosylation type ic
    n1=en:leucinosis | n2=en:congenital disorder of glycosylation type ic | rel=r_associated | relid=0 | w=34
  791. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:congenital disorder of glycosylation type ig
    n1=en:leucinosis | n2=en:congenital disorder of glycosylation type ig | rel=r_associated | relid=0 | w=34
  792. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:congenital dyserythropoietic anemia
    n1=en:leucinosis | n2=en:congenital dyserythropoietic anemia | rel=r_associated | relid=0 | w=34
  793. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:congenital fiber-type disproportion
    n1=en:leucinosis | n2=en:congenital fiber-type disproportion | rel=r_associated | relid=0 | w=34
  794. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:congenital sucrase-isomaltase deficiency
    n1=en:leucinosis | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=34
  795. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:crisponi syndrome
    n1=en:leucinosis | n2=en:crisponi syndrome | rel=r_associated | relid=0 | w=34
  796. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:cryptophthalmos syndrome
    n1=en:leucinosis | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=34
  797. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:cystathionine beta-synthase deficiency disease
    n1=en:leucinosis | n2=en:cystathionine beta-synthase deficiency disease | rel=r_associated | relid=0 | w=34
  798. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:deafness, autosomal recessive 1a
    n1=en:leucinosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  799. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:deafness, autosomal recessive 49
    n1=en:leucinosis | n2=en:deafness, autosomal recessive 49 | rel=r_associated | relid=0 | w=34
  800. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:deafness, congenital, with inner ear agenesis, microtia, and microdontia
    n1=en:leucinosis | n2=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | rel=r_associated | relid=0 | w=34
  801. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:deafness, sensorineural, and male infertility
    n1=en:leucinosis | n2=en:deafness, sensorineural, and male infertility | rel=r_associated | relid=0 | w=34
  802. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:deficiency of glucosyltransferase 1
    n1=en:leucinosis | n2=en:deficiency of glucosyltransferase 1 | rel=r_associated | relid=0 | w=34
  803. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:dent disease
    n1=en:leucinosis | n2=en:dent disease | rel=r_associated | relid=0 | w=34
  804. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:diffuse idiopathic skeletal hyperostosis
    n1=en:leucinosis | n2=en:diffuse idiopathic skeletal hyperostosis | rel=r_associated | relid=0 | w=34
  805. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:disorder of amino acid and organic acid metabolism
    n1=en:leucinosis | n2=en:disorder of amino acid and organic acid metabolism | rel=r_associated | relid=0 | w=34
  806. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:disorder of creatine synthesis
    n1=en:leucinosis | n2=en:disorder of creatine synthesis | rel=r_associated | relid=0 | w=34
  807. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:disorder of valine metabolism
    n1=en:leucinosis | n2=en:disorder of valine metabolism | rel=r_associated | relid=0 | w=34
  808. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:duane syndrome
    n1=en:leucinosis | n2=en:duane syndrome | rel=r_associated | relid=0 | w=34
  809. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:dubowitz syndrome
    n1=en:leucinosis | n2=en:dubowitz syndrome | rel=r_associated | relid=0 | w=34
  810. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency
    n1=en:leucinosis | n2=en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency | rel=r_associated | relid=0 | w=34
  811. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:encephalocele
    n1=en:leucinosis | n2=en:encephalocele | rel=r_associated | relid=0 | w=34
  812. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:ethanolaminosis
    n1=en:leucinosis | n2=en:ethanolaminosis | rel=r_associated | relid=0 | w=34
  813. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:familial c3b inhibitor deficiency syndrome
    n1=en:leucinosis | n2=en:familial c3b inhibitor deficiency syndrome | rel=r_associated | relid=0 | w=34
  814. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:familial hypothyroidism
    n1=en:leucinosis | n2=en:familial hypothyroidism | rel=r_associated | relid=0 | w=34
  815. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:familial primary hypomagnesemia
    n1=en:leucinosis | n2=en:familial primary hypomagnesemia | rel=r_associated | relid=0 | w=34
  816. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:familial testicular germ cell tumor
    n1=en:leucinosis | n2=en:familial testicular germ cell tumor | rel=r_associated | relid=0 | w=34
  817. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:farber lipogranulomatosis
    n1=en:leucinosis | n2=en:farber lipogranulomatosis | rel=r_associated | relid=0 | w=34
  818. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:fatal infantile lactic acidosis with methylmalonic aciduria
    n1=en:leucinosis | n2=en:fatal infantile lactic acidosis with methylmalonic aciduria | rel=r_associated | relid=0 | w=34
  819. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:fronto-facio-nasal dysplasia
    n1=en:leucinosis | n2=en:fronto-facio-nasal dysplasia | rel=r_associated | relid=0 | w=34
  820. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:frontonasal dysplasia
    n1=en:leucinosis | n2=en:frontonasal dysplasia | rel=r_associated | relid=0 | w=34
  821. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:fructose-1,6-bisphosphatase deficiency
    n1=en:leucinosis | n2=en:fructose-1,6-bisphosphatase deficiency | rel=r_associated | relid=0 | w=34
  822. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:goldenhar syndrome
    n1=en:leucinosis | n2=en:goldenhar syndrome | rel=r_associated | relid=0 | w=34
  823. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:gracile syndrome (disorder)
    n1=en:leucinosis | n2=en:gracile syndrome (disorder) | rel=r_associated | relid=0 | w=34
  824. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:gyrate atrophy
    n1=en:leucinosis | n2=en:gyrate atrophy | rel=r_associated | relid=0 | w=34
  825. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:hallucination
    n1=en:leucinosis | n2=en:hallucination | rel=r_associated | relid=0 | w=34
  826. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:hereditary breast/ovarian cancer - brca2
    n1=en:leucinosis | n2=en:hereditary breast/ovarian cancer - brca2 | rel=r_associated | relid=0 | w=34
  827. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:hereditary factor x deficiency disease
    n1=en:leucinosis | n2=en:hereditary factor x deficiency disease | rel=r_associated | relid=0 | w=34
  828. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:hereditary fructose intolerance
    n1=en:leucinosis | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=34
  829. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:hereditary orotic aciduria
    n1=en:leucinosis | n2=en:hereditary orotic aciduria | rel=r_associated | relid=0 | w=34
  830. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:hereditary peripheral nervous system disorder
    n1=en:leucinosis | n2=en:hereditary peripheral nervous system disorder | rel=r_associated | relid=0 | w=34
  831. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:heritable pulmonary arterial hypertension
    n1=en:leucinosis | n2=en:heritable pulmonary arterial hypertension | rel=r_associated | relid=0 | w=34
  832. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:hnsha due to pyrimidine-5'-nucleotidase deficiency
    n1=en:leucinosis | n2=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | rel=r_associated | relid=0 | w=34
  833. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:holoprosencephaly
    n1=en:leucinosis | n2=en:holoprosencephaly | rel=r_associated | relid=0 | w=34
  834. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:hydroxyprolinemia
    n1=en:leucinosis | n2=en:hydroxyprolinemia | rel=r_associated | relid=0 | w=34
  835. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:hyperprolinemia
    n1=en:leucinosis | n2=en:hyperprolinemia | rel=r_associated | relid=0 | w=34
  836. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:inherited factor ii deficiency
    n1=en:leucinosis | n2=en:inherited factor ii deficiency | rel=r_associated | relid=0 | w=34
  837. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:inherited metabolic disorder of nervous system
    n1=en:leucinosis | n2=en:inherited metabolic disorder of nervous system | rel=r_associated | relid=0 | w=34
  838. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:inherited predisposition to essential thrombocythemia
    n1=en:leucinosis | n2=en:inherited predisposition to essential thrombocythemia | rel=r_associated | relid=0 | w=34
  839. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:interleukin-1 receptor-associated kinase 4 deficiency
    n1=en:leucinosis | n2=en:interleukin-1 receptor-associated kinase 4 deficiency | rel=r_associated | relid=0 | w=34
  840. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:intestinal epithelial dysplasia
    n1=en:leucinosis | n2=en:intestinal epithelial dysplasia | rel=r_associated | relid=0 | w=34
  841. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:isaacs syndrome
    n1=en:leucinosis | n2=en:isaacs syndrome | rel=r_associated | relid=0 | w=34
  842. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:ketonuria
    n1=en:leucinosis | n2=en:ketonuria | rel=r_associated | relid=0 | w=34
  843. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:klippel-feil syndrome
    n1=en:leucinosis | n2=en:klippel-feil syndrome | rel=r_associated | relid=0 | w=34
  844. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:leber hereditary optic atrophy
    n1=en:leucinosis | n2=en:leber hereditary optic atrophy | rel=r_associated | relid=0 | w=34
  845. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:lethal congenital contracture syndrome type 3
    n1=en:leucinosis | n2=en:lethal congenital contracture syndrome type 3 | rel=r_associated | relid=0 | w=34
  846. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:liddle syndrome
    n1=en:leucinosis | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=34
  847. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:life-threatening metabolic decompensation
    n1=en:leucinosis | n2=en:life-threatening metabolic decompensation | rel=r_associated | relid=0 | w=34
  848. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:loeys-dietz syndrome
    n1=en:leucinosis | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=34
  849. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:lysosomal storage disease
    n1=en:leucinosis | n2=en:lysosomal storage disease | rel=r_associated | relid=0 | w=34
  850. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:machado-joseph disease
    n1=en:leucinosis | n2=en:machado-joseph disease | rel=r_associated | relid=0 | w=34
  851. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:malakoplakia
    n1=en:leucinosis | n2=en:malakoplakia | rel=r_associated | relid=0 | w=34
  852. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:marburg virus disease
    n1=en:leucinosis | n2=en:marburg virus disease | rel=r_associated | relid=0 | w=34
  853. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:melas syndrome
    n1=en:leucinosis | n2=en:melas syndrome | rel=r_associated | relid=0 | w=34
  854. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency
    n1=en:leucinosis | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | rel=r_associated | relid=0 | w=34
  855. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:morquio syndrome
    n1=en:leucinosis | n2=en:morquio syndrome | rel=r_associated | relid=0 | w=34
  856. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:multiple endocrine neoplasia
    n1=en:leucinosis | n2=en:multiple endocrine neoplasia | rel=r_associated | relid=0 | w=34
  857. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:neurodegeneration with brain iron accumulation 4
    n1=en:leucinosis | n2=en:neurodegeneration with brain iron accumulation 4 | rel=r_associated | relid=0 | w=34
  858. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:neuromyelitis optica
    n1=en:leucinosis | n2=en:neuromyelitis optica | rel=r_associated | relid=0 | w=34
  859. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:nevoid basal cell carcinoma syndrome
    n1=en:leucinosis | n2=en:nevoid basal cell carcinoma syndrome | rel=r_associated | relid=0 | w=34
  860. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:niemann-pick disease
    n1=en:leucinosis | n2=en:niemann-pick disease | rel=r_associated | relid=0 | w=34
  861. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:nonaka myopathy
    n1=en:leucinosis | n2=en:nonaka myopathy | rel=r_associated | relid=0 | w=34
  862. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:olivopontocerebellar atrophy
    n1=en:leucinosis | n2=en:olivopontocerebellar atrophy | rel=r_associated | relid=0 | w=34
  863. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:opitz trigonocephaly syndrome
    n1=en:leucinosis | n2=en:opitz trigonocephaly syndrome | rel=r_associated | relid=0 | w=34
  864. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:orofaciodigital syndrome type 1
    n1=en:leucinosis | n2=en:orofaciodigital syndrome type 1 | rel=r_associated | relid=0 | w=34
  865. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:pancreatitis
    n1=en:leucinosis | n2=en:pancreatitis | rel=r_associated | relid=0 | w=34
  866. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:paroxysmal extreme pain disorder
    n1=en:leucinosis | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=34
  867. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:pelizaeus-merzbacher disease
    n1=en:leucinosis | n2=en:pelizaeus-merzbacher disease | rel=r_associated | relid=0 | w=34
  868. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:pharmacotherapeutic
    n1=en:leucinosis | n2=en:pharmacotherapeutic | rel=r_associated | relid=0 | w=34
  869. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:physiopathological
    n1=en:leucinosis | n2=en:physiopathological | rel=r_associated | relid=0 | w=34
  870. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:pityriasis rubra pilaris
    n1=en:leucinosis | n2=en:pityriasis rubra pilaris | rel=r_associated | relid=0 | w=34
  871. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:premature aging syndrome
    n1=en:leucinosis | n2=en:premature aging syndrome | rel=r_associated | relid=0 | w=34
  872. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:primary hypertrophic osteoarthropathy
    n1=en:leucinosis | n2=en:primary hypertrophic osteoarthropathy | rel=r_associated | relid=0 | w=34
  873. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88
    n1=en:leucinosis | n2=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | rel=r_associated | relid=0 | w=34
  874. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:reardon hall slaney syndrome
    n1=en:leucinosis | n2=en:reardon hall slaney syndrome | rel=r_associated | relid=0 | w=34
  875. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:retinitis pigmentosa
    n1=en:leucinosis | n2=en:retinitis pigmentosa | rel=r_associated | relid=0 | w=34
  876. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:retinitis punctata albescens (disorder)
    n1=en:leucinosis | n2=en:retinitis punctata albescens (disorder) | rel=r_associated | relid=0 | w=34
  877. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:revesz syndrome (disorder)
    n1=en:leucinosis | n2=en:revesz syndrome (disorder) | rel=r_associated | relid=0 | w=34
  878. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:robinow syndrome
    n1=en:leucinosis | n2=en:robinow syndrome | rel=r_associated | relid=0 | w=34
  879. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:scleromyxedema
    n1=en:leucinosis | n2=en:scleromyxedema | rel=r_associated | relid=0 | w=34
  880. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:sonoda syndrome
    n1=en:leucinosis | n2=en:sonoda syndrome | rel=r_associated | relid=0 | w=34
  881. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:spondyloepimetaphyseal dysplasia with joint laxity type 2
    n1=en:leucinosis | n2=en:spondyloepimetaphyseal dysplasia with joint laxity type 2 | rel=r_associated | relid=0 | w=34
  882. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:status epilepticus
    n1=en:leucinosis | n2=en:status epilepticus | rel=r_associated | relid=0 | w=34
  883. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:subacute sclerosing panencephalitis
    n1=en:leucinosis | n2=en:subacute sclerosing panencephalitis | rel=r_associated | relid=0 | w=34
  884. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:sudden infant death with dysgenesis of the testes syndrome
    n1=en:leucinosis | n2=en:sudden infant death with dysgenesis of the testes syndrome | rel=r_associated | relid=0 | w=34
  885. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:sudden unexplained death in childhood
    n1=en:leucinosis | n2=en:sudden unexplained death in childhood | rel=r_associated | relid=0 | w=34
  886. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:tangier disease
    n1=en:leucinosis | n2=en:tangier disease | rel=r_associated | relid=0 | w=34
  887. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:tetraamelia multiple malformations
    n1=en:leucinosis | n2=en:tetraamelia multiple malformations | rel=r_associated | relid=0 | w=34
  888. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:thyroid hormone resistance syndrome
    n1=en:leucinosis | n2=en:thyroid hormone resistance syndrome | rel=r_associated | relid=0 | w=34
  889. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:transcobalamin ii deficiency
    n1=en:leucinosis | n2=en:transcobalamin ii deficiency | rel=r_associated | relid=0 | w=34
  890. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:turner syndrome
    n1=en:leucinosis | n2=en:turner syndrome | rel=r_associated | relid=0 | w=34
  891. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:tyrosinemia
    n1=en:leucinosis | n2=en:tyrosinemia | rel=r_associated | relid=0 | w=34
  892. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:unspecified mental retardation; other impairments of behaviour
    n1=en:leucinosis | n2=en:unspecified mental retardation; other impairments of behaviour | rel=r_associated | relid=0 | w=34
  893. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:variegate porphyria
    n1=en:leucinosis | n2=en:variegate porphyria | rel=r_associated | relid=0 | w=34
  894. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:white matter signal abnormalities in various brain regions
    n1=en:leucinosis | n2=en:white matter signal abnormalities in various brain regions | rel=r_associated | relid=0 | w=34
  895. en:leucinosis -- r_associated #0: 34 / 0.654 -> en:xerophthalmia
    n1=en:leucinosis | n2=en:xerophthalmia | rel=r_associated | relid=0 | w=34
  896. en:leucinosis -- r_associated #0: 34 / 0.654 -> eu en milieu de jet
    n1=en:leucinosis | n2=eu en milieu de jet | rel=r_associated | relid=0 | w=34
  897. en:leucinosis -- r_associated #0: 34 / 0.654 -> gène
    n1=en:leucinosis | n2=gène | rel=r_associated | relid=0 | w=34
  898. en:leucinosis -- r_associated #0: 34 / 0.654 -> maladie des urines à l'odeur de sirop d'érable
    n1=en:leucinosis | n2=maladie des urines à l'odeur de sirop d'érable | rel=r_associated | relid=0 | w=34
  899. en:leucinosis -- r_associated #0: 34 / 0.654 -> maladie des urines avec odeur de sirop erable
    n1=en:leucinosis | n2=maladie des urines avec odeur de sirop erable | rel=r_associated | relid=0 | w=34
  900. en:leucinosis -- r_associated #0: 34 / 0.654 -> maladie du sirop d'érable
    n1=en:leucinosis | n2=maladie du sirop d'érable | rel=r_associated | relid=0 | w=34
  901. en:leucinosis -- r_associated #0: 34 / 0.654 -> maladie rare
    n1=en:leucinosis | n2=maladie rare | rel=r_associated | relid=0 | w=34
  902. en:leucinosis -- r_associated #0: 34 / 0.654 -> phénylcétonurie
    n1=en:leucinosis | n2=phénylcétonurie | rel=r_associated | relid=0 | w=34
  903. en:leucinosis -- r_associated #0: 34 / 0.654 -> sirop d'érable (urine à odeur de)
    n1=en:leucinosis | n2=sirop d'érable (urine à odeur de) | rel=r_associated | relid=0 | w=34
  904. en:leucinosis -- r_associated #0: 33 / 0.635 -> Beauvieux (hérédité du syndrome de)
    n1=en:leucinosis | n2=Beauvieux (hérédité du syndrome de) | rel=r_associated | relid=0 | w=33
  905. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:(5) dihydrolipoyl dehydrogenase (e3)-deficient
    n1=en:leucinosis | n2=en:(5) dihydrolipoyl dehydrogenase (e3)-deficient | rel=r_associated | relid=0 | w=33
  906. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:3-methylglutaconic aciduria type 3
    n1=en:leucinosis | n2=en:3-methylglutaconic aciduria type 3 | rel=r_associated | relid=0 | w=33
  907. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:achard syndrome
    n1=en:leucinosis | n2=en:achard syndrome | rel=r_associated | relid=0 | w=33
  908. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:adenine phosphoribosyltransferase deficiency
    n1=en:leucinosis | n2=en:adenine phosphoribosyltransferase deficiency | rel=r_associated | relid=0 | w=33
  909. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:alagille syndrome
    n1=en:leucinosis | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=33
  910. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:amino acid/carbohydrate metabolic disorder
    n1=en:leucinosis | n2=en:amino acid/carbohydrate metabolic disorder | rel=r_associated | relid=0 | w=33
  911. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:argininosuccinic aciduria
    n1=en:leucinosis | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=33
  912. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:aspartylglycosaminuria
    n1=en:leucinosis | n2=en:aspartylglycosaminuria | rel=r_associated | relid=0 | w=33
  913. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:ataxia telangiectasia syndrome
    n1=en:leucinosis | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=33
  914. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:autosomal dominant disorder
    n1=en:leucinosis | n2=en:autosomal dominant disorder | rel=r_associated | relid=0 | w=33
  915. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:autosomal recessive asexual dwarfism
    n1=en:leucinosis | n2=en:autosomal recessive asexual dwarfism | rel=r_associated | relid=0 | w=33
  916. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:bowen-conradi syndrome
    n1=en:leucinosis | n2=en:bowen-conradi syndrome | rel=r_associated | relid=0 | w=33
  917. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:brca1 mutation carrier
    n1=en:leucinosis | n2=en:brca1 mutation carrier | rel=r_associated | relid=0 | w=33
  918. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:brca2 mutation carrier
    n1=en:leucinosis | n2=en:brca2 mutation carrier | rel=r_associated | relid=0 | w=33
  919. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:calciphylaxis
    n1=en:leucinosis | n2=en:calciphylaxis | rel=r_associated | relid=0 | w=33
  920. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:campomelic dysplasia
    n1=en:leucinosis | n2=en:campomelic dysplasia | rel=r_associated | relid=0 | w=33
  921. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:camurati-engelmann syndrome
    n1=en:leucinosis | n2=en:camurati-engelmann syndrome | rel=r_associated | relid=0 | w=33
  922. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:cardiofaciocutaneous syndrome
    n1=en:leucinosis | n2=en:cardiofaciocutaneous syndrome | rel=r_associated | relid=0 | w=33
  923. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:carnosinemia
    n1=en:leucinosis | n2=en:carnosinemia | rel=r_associated | relid=0 | w=33
  924. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:caused by mutation in the branched chain keto acid dehydrogenase e1, beta polypeptide gene (bckdhb, 248611.0001)
    n1=en:leucinosis | n2=en:caused by mutation in the branched chain keto acid dehydrogenase e1, beta polypeptide gene (bckdhb, 248611.0001) | rel=r_associated | relid=0 | w=33
  925. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:chorea
    n1=en:leucinosis | n2=en:chorea | rel=r_associated | relid=0 | w=33
  926. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:citrullinemia
    n1=en:leucinosis | n2=en:citrullinemia | rel=r_associated | relid=0 | w=33
  927. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:codas syndrome
    n1=en:leucinosis | n2=en:codas syndrome | rel=r_associated | relid=0 | w=33
  928. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:coffin-siris syndrome
    n1=en:leucinosis | n2=en:coffin-siris syndrome | rel=r_associated | relid=0 | w=33
  929. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:combined malonic and methylmalonic aciduria
    n1=en:leucinosis | n2=en:combined malonic and methylmalonic aciduria | rel=r_associated | relid=0 | w=33
  930. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:congenital dyserythropoietic anemia, type ii
    n1=en:leucinosis | n2=en:congenital dyserythropoietic anemia, type ii | rel=r_associated | relid=0 | w=33
  931. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:congenital neutropenia
    n1=en:leucinosis | n2=en:congenital neutropenia | rel=r_associated | relid=0 | w=33
  932. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:congenital t-cell immunodeficiency
    n1=en:leucinosis | n2=en:congenital t-cell immunodeficiency | rel=r_associated | relid=0 | w=33
  933. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:cranioectodermal dysplasia
    n1=en:leucinosis | n2=en:cranioectodermal dysplasia | rel=r_associated | relid=0 | w=33
  934. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:cytochrome-c oxidase deficiency
    n1=en:leucinosis | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=33
  935. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:d-bifunctional protein deficiency
    n1=en:leucinosis | n2=en:d-bifunctional protein deficiency | rel=r_associated | relid=0 | w=33
  936. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:dentatorubral-pallidoluysian atrophy
    n1=en:leucinosis | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=33
  937. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:disorder of carnitine metabolism, unspecified
    n1=en:leucinosis | n2=en:disorder of carnitine metabolism, unspecified | rel=r_associated | relid=0 | w=33
  938. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:dna repair disorder
    n1=en:leucinosis | n2=en:dna repair disorder | rel=r_associated | relid=0 | w=33
  939. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:dubin-johnson syndrome
    n1=en:leucinosis | n2=en:dubin-johnson syndrome | rel=r_associated | relid=0 | w=33
  940. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:ehlers-danlos syndrome
    n1=en:leucinosis | n2=en:ehlers-danlos syndrome | rel=r_associated | relid=0 | w=33
  941. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:ehlers-danlos syndrome, arthrochalasia type
    n1=en:leucinosis | n2=en:ehlers-danlos syndrome, arthrochalasia type | rel=r_associated | relid=0 | w=33
  942. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:enterokinase deficiency
    n1=en:leucinosis | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=33
  943. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:erythrokeratodermia variabilis
    n1=en:leucinosis | n2=en:erythrokeratodermia variabilis | rel=r_associated | relid=0 | w=33
  944. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:erythromelalgia
    n1=en:leucinosis | n2=en:erythromelalgia | rel=r_associated | relid=0 | w=33
  945. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:familial isolated hyperparathyroidism
    n1=en:leucinosis | n2=en:familial isolated hyperparathyroidism | rel=r_associated | relid=0 | w=33
  946. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:familial juvenile nephronophthisis
    n1=en:leucinosis | n2=en:familial juvenile nephronophthisis | rel=r_associated | relid=0 | w=33
  947. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:familial multiple myeloma
    n1=en:leucinosis | n2=en:familial multiple myeloma | rel=r_associated | relid=0 | w=33
  948. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:familial non-medullary thyroid cancer
    n1=en:leucinosis | n2=en:familial non-medullary thyroid cancer | rel=r_associated | relid=0 | w=33
  949. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:feeding problem
    n1=en:leucinosis | n2=en:feeding problem | rel=r_associated | relid=0 | w=33
  950. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:ferrochelatase deficiency
    n1=en:leucinosis | n2=en:ferrochelatase deficiency | rel=r_associated | relid=0 | w=33
  951. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:fibular hypoplasia and complex brachydactyly
    n1=en:leucinosis | n2=en:fibular hypoplasia and complex brachydactyly | rel=r_associated | relid=0 | w=33
  952. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:fraser syndrome
    n1=en:leucinosis | n2=en:fraser syndrome | rel=r_associated | relid=0 | w=33
  953. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:frontotemporal dementia
    n1=en:leucinosis | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=33
  954. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:genetic brain disorders
    n1=en:leucinosis | n2=en:genetic brain disorders | rel=r_associated | relid=0 | w=33
  955. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:genu varum
    n1=en:leucinosis | n2=en:genu varum | rel=r_associated | relid=0 | w=33
  956. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:glycogen storage disease type i
    n1=en:leucinosis | n2=en:glycogen storage disease type i | rel=r_associated | relid=0 | w=33
  957. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:gynatresia
    n1=en:leucinosis | n2=en:gynatresia | rel=r_associated | relid=0 | w=33
  958. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:hereditary cerebral amyloid angiopathy, icelandic type
    n1=en:leucinosis | n2=en:hereditary cerebral amyloid angiopathy, icelandic type | rel=r_associated | relid=0 | w=33
  959. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:hereditary retinoblastoma
    n1=en:leucinosis | n2=en:hereditary retinoblastoma | rel=r_associated | relid=0 | w=33
  960. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:hereditary thyroid gland medullary carcinoma
    n1=en:leucinosis | n2=en:hereditary thyroid gland medullary carcinoma | rel=r_associated | relid=0 | w=33
  961. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:historical aspects qualifier
    n1=en:leucinosis | n2=en:historical aspects qualifier | rel=r_associated | relid=0 | w=33
  962. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:hnsha due to glutathione synthetase deficiency
    n1=en:leucinosis | n2=en:hnsha due to glutathione synthetase deficiency | rel=r_associated | relid=0 | w=33
  963. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:holt-oram syndrome
    n1=en:leucinosis | n2=en:holt-oram syndrome | rel=r_associated | relid=0 | w=33
  964. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:hydroa vacciniforme
    n1=en:leucinosis | n2=en:hydroa vacciniforme | rel=r_associated | relid=0 | w=33
  965. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:hyperandrogenism due to non-classic 21-hydroxylase deficiency
    n1=en:leucinosis | n2=en:hyperandrogenism due to non-classic 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=33
  966. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:hyperleucine-isoleucinemia
    n1=en:leucinosis | n2=en:hyperleucine-isoleucinemia | rel=r_associated | relid=0 | w=33
  967. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:hyperleucinemia
    n1=en:leucinosis | n2=en:hyperleucinemia | rel=r_associated | relid=0 | w=33
  968. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:hypermanganesemia with dystonia polycythemia and cirrhosis
    n1=en:leucinosis | n2=en:hypermanganesemia with dystonia polycythemia and cirrhosis | rel=r_associated | relid=0 | w=33
  969. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:hyperornithinemia
    n1=en:leucinosis | n2=en:hyperornithinemia | rel=r_associated | relid=0 | w=33
  970. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:hypokalemia, familial
    n1=en:leucinosis | n2=en:hypokalemia, familial | rel=r_associated | relid=0 | w=33
  971. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:inborn error of glutathione metabolism
    n1=en:leucinosis | n2=en:inborn error of glutathione metabolism | rel=r_associated | relid=0 | w=33
  972. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:inborn errors of steroid synthesis
    n1=en:leucinosis | n2=en:inborn errors of steroid synthesis | rel=r_associated | relid=0 | w=33
  973. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:increased aromatase activity
    n1=en:leucinosis | n2=en:increased aromatase activity | rel=r_associated | relid=0 | w=33
  974. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:infantile globoid cell leukodystrophy
    n1=en:leucinosis | n2=en:infantile globoid cell leukodystrophy | rel=r_associated | relid=0 | w=33
  975. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:infantile hypophosphatasia
    n1=en:leucinosis | n2=en:infantile hypophosphatasia | rel=r_associated | relid=0 | w=33
  976. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:infantile neuroaxonal dystrophy
    n1=en:leucinosis | n2=en:infantile neuroaxonal dystrophy | rel=r_associated | relid=0 | w=33
  977. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:isolated hyperchlorhidrosis
    n1=en:leucinosis | n2=en:isolated hyperchlorhidrosis | rel=r_associated | relid=0 | w=33
  978. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:karandikar maria kamble syndrome
    n1=en:leucinosis | n2=en:karandikar maria kamble syndrome | rel=r_associated | relid=0 | w=33
  979. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:klippel-trenaunay-weber syndrome
    n1=en:leucinosis | n2=en:klippel-trenaunay-weber syndrome | rel=r_associated | relid=0 | w=33
  980. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:knobloch syndrome
    n1=en:leucinosis | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=33
  981. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:korsakoff syndrome
    n1=en:leucinosis | n2=en:korsakoff syndrome | rel=r_associated | relid=0 | w=33
  982. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:lactic acidosis in e3-deficiency
    n1=en:leucinosis | n2=en:lactic acidosis in e3-deficiency | rel=r_associated | relid=0 | w=33
  983. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:lateral medullary syndrome
    n1=en:leucinosis | n2=en:lateral medullary syndrome | rel=r_associated | relid=0 | w=33
  984. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:leigh disease
    n1=en:leucinosis | n2=en:leigh disease | rel=r_associated | relid=0 | w=33
  985. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:leptospirosis
    n1=en:leucinosis | n2=en:leptospirosis | rel=r_associated | relid=0 | w=33
  986. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:lujan fryns syndrome
    n1=en:leucinosis | n2=en:lujan fryns syndrome | rel=r_associated | relid=0 | w=33
  987. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:malignant hyperthermia syndrome
    n1=en:leucinosis | n2=en:malignant hyperthermia syndrome | rel=r_associated | relid=0 | w=33
  988. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:maple syrup urine disease:imp:pt:bld.dot:nom
    n1=en:leucinosis | n2=en:maple syrup urine disease:imp:pt:bld.dot:nom | rel=r_associated | relid=0 | w=33
  989. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:maple-tree syrup disease
    n1=en:leucinosis | n2=en:maple-tree syrup disease | rel=r_associated | relid=0 | w=33
  990. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:marfanoid mental retardation syndrome
    n1=en:leucinosis | n2=en:marfanoid mental retardation syndrome | rel=r_associated | relid=0 | w=33
  991. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:melorheostosis
    n1=en:leucinosis | n2=en:melorheostosis | rel=r_associated | relid=0 | w=33
  992. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:methylenetetrahydrofolate reductase deficiency
    n1=en:leucinosis | n2=en:methylenetetrahydrofolate reductase deficiency | rel=r_associated | relid=0 | w=33
  993. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:microbiological
    n1=en:leucinosis | n2=en:microbiological | rel=r_associated | relid=0 | w=33
  994. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:microcephaly and chorioretinopathy, autosomal recessive, type 1
    n1=en:leucinosis | n2=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | rel=r_associated | relid=0 | w=33
  995. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:neurotoxicity syndrome
    n1=en:leucinosis | n2=en:neurotoxicity syndrome | rel=r_associated | relid=0 | w=33
  996. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:oculocerebrorenal syndrome
    n1=en:leucinosis | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=33
  997. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:other mental retardation
    n1=en:leucinosis | n2=en:other mental retardation | rel=r_associated | relid=0 | w=33
  998. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:other specified disorders of amino-acid transport and metabolism
    n1=en:leucinosis | n2=en:other specified disorders of amino-acid transport and metabolism | rel=r_associated | relid=0 | w=33
  999. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:pancreatic colipase deficiency
    n1=en:leucinosis | n2=en:pancreatic colipase deficiency | rel=r_associated | relid=0 | w=33
  1000. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:pelizaeus merzbacher like disease
    n1=en:leucinosis | n2=en:pelizaeus merzbacher like disease | rel=r_associated | relid=0 | w=33
  1001. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:pentosuria
    n1=en:leucinosis | n2=en:pentosuria | rel=r_associated | relid=0 | w=33
  1002. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:persistent mullerian duct syndrome
    n1=en:leucinosis | n2=en:persistent mullerian duct syndrome | rel=r_associated | relid=0 | w=33
  1003. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:pierre robin syndrome
    n1=en:leucinosis | n2=en:pierre robin syndrome | rel=r_associated | relid=0 | w=33
  1004. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:pontocerebellar hypoplasia type 2
    n1=en:leucinosis | n2=en:pontocerebellar hypoplasia type 2 | rel=r_associated | relid=0 | w=33
  1005. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:porokeratosis
    n1=en:leucinosis | n2=en:porokeratosis | rel=r_associated | relid=0 | w=33
  1006. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:porphyria cutanea tarda
    n1=en:leucinosis | n2=en:porphyria cutanea tarda | rel=r_associated | relid=0 | w=33
  1007. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:prader-willi habitus, osteopenia, and camptodactyly
    n1=en:leucinosis | n2=en:prader-willi habitus, osteopenia, and camptodactyly | rel=r_associated | relid=0 | w=33
  1008. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:primary carnitine deficiency
    n1=en:leucinosis | n2=en:primary carnitine deficiency | rel=r_associated | relid=0 | w=33
  1009. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:primary hyperoxaluria
    n1=en:leucinosis | n2=en:primary hyperoxaluria | rel=r_associated | relid=0 | w=33
  1010. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:propionic acidemia
    n1=en:leucinosis | n2=en:propionic acidemia | rel=r_associated | relid=0 | w=33
  1011. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:proteus syndrome
    n1=en:leucinosis | n2=en:proteus syndrome | rel=r_associated | relid=0 | w=33
  1012. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:pyruvate kinase deficiency
    n1=en:leucinosis | n2=en:pyruvate kinase deficiency | rel=r_associated | relid=0 | w=33
  1013. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:retinoschisis
    n1=en:leucinosis | n2=en:retinoschisis | rel=r_associated | relid=0 | w=33
  1014. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:russell-silver syndrome
    n1=en:leucinosis | n2=en:russell-silver syndrome | rel=r_associated | relid=0 | w=33
  1015. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:saito kuba tsuruta syndrome
    n1=en:leucinosis | n2=en:saito kuba tsuruta syndrome | rel=r_associated | relid=0 | w=33
  1016. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:septo-optic dysplasia
    n1=en:leucinosis | n2=en:septo-optic dysplasia | rel=r_associated | relid=0 | w=33
  1017. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:shprintzen-goldberg craniosynostosis syndrome
    n1=en:leucinosis | n2=en:shprintzen-goldberg craniosynostosis syndrome | rel=r_associated | relid=0 | w=33
  1018. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:sickle cell disease
    n1=en:leucinosis | n2=en:sickle cell disease | rel=r_associated | relid=0 | w=33
  1019. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:smith-mccort dysplasia
    n1=en:leucinosis | n2=en:smith-mccort dysplasia | rel=r_associated | relid=0 | w=33
  1020. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:spastic paraplegia 15, autosomal recessive
    n1=en:leucinosis | n2=en:spastic paraplegia 15, autosomal recessive | rel=r_associated | relid=0 | w=33
  1021. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:spondyloepiphyseal dysplasia, omani type
    n1=en:leucinosis | n2=en:spondyloepiphyseal dysplasia, omani type | rel=r_associated | relid=0 | w=33
  1022. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:surgical aspects
    n1=en:leucinosis | n2=en:surgical aspects | rel=r_associated | relid=0 | w=33
  1023. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:taxonomic
    n1=en:leucinosis | n2=en:taxonomic | rel=r_associated | relid=0 | w=33
  1024. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:therapeutic aspects
    n1=en:leucinosis | n2=en:therapeutic aspects | rel=r_associated | relid=0 | w=33
  1025. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:tracheobronchomalacia
    n1=en:leucinosis | n2=en:tracheobronchomalacia | rel=r_associated | relid=0 | w=33
  1026. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:tracheobronchomegaly
    n1=en:leucinosis | n2=en:tracheobronchomegaly | rel=r_associated | relid=0 | w=33
  1027. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:transient global amnesia
    n1=en:leucinosis | n2=en:transient global amnesia | rel=r_associated | relid=0 | w=33
  1028. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:trigger finger disorder
    n1=en:leucinosis | n2=en:trigger finger disorder | rel=r_associated | relid=0 | w=33
  1029. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:tylosis with esophageal cancer
    n1=en:leucinosis | n2=en:tylosis with esophageal cancer | rel=r_associated | relid=0 | w=33
  1030. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:tyrosinemia, type iii
    n1=en:leucinosis | n2=en:tyrosinemia, type iii | rel=r_associated | relid=0 | w=33
  1031. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:valinemia
    n1=en:leucinosis | n2=en:valinemia | rel=r_associated | relid=0 | w=33
  1032. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:van der woude syndrome
    n1=en:leucinosis | n2=en:van der woude syndrome | rel=r_associated | relid=0 | w=33
  1033. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:verloes bourguignon syndrome
    n1=en:leucinosis | n2=en:verloes bourguignon syndrome | rel=r_associated | relid=0 | w=33
  1034. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:xanthinuria, type i
    n1=en:leucinosis | n2=en:xanthinuria, type i | rel=r_associated | relid=0 | w=33
  1035. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:xyy syndrome
    n1=en:leucinosis | n2=en:xyy syndrome | rel=r_associated | relid=0 | w=33
  1036. en:leucinosis -- r_associated #0: 33 / 0.635 -> en:yellow nail syndrome
    n1=en:leucinosis | n2=en:yellow nail syndrome | rel=r_associated | relid=0 | w=33
  1037. en:leucinosis -- r_associated #0: 33 / 0.635 -> leucine
    n1=en:leucinosis | n2=leucine | rel=r_associated | relid=0 | w=33
  1038. en:leucinosis -- r_associated #0: 33 / 0.635 -> leucinose thiamine-sensible
    n1=en:leucinosis | n2=leucinose thiamine-sensible | rel=r_associated | relid=0 | w=33
  1039. en:leucinosis -- r_associated #0: 33 / 0.635 -> Médecine
    n1=en:leucinosis | n2=Médecine | rel=r_associated | relid=0 | w=33
  1040. en:leucinosis -- r_associated #0: 33 / 0.635 -> syndrome de Beauvieux
    n1=en:leucinosis | n2=syndrome de Beauvieux | rel=r_associated | relid=0 | w=33
  1041. en:leucinosis -- r_associated #0: 32 / 0.615 -> BCKDHA gene l.angl. pour
    n1=en:leucinosis | n2=BCKDHA gene l.angl. pour | rel=r_associated | relid=0 | w=32
  1042. en:leucinosis -- r_associated #0: 32 / 0.615 -> céto
    n1=en:leucinosis | n2=céto | rel=r_associated | relid=0 | w=32
  1043. en:leucinosis -- r_associated #0: 32 / 0.615 -> cétoacidurie à chaînes ramifiées
    n1=en:leucinosis | n2=cétoacidurie à chaînes ramifiées | rel=r_associated | relid=0 | w=32
  1044. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:(4) thiamine-responsive form
    n1=en:leucinosis | n2=en:(4) thiamine-responsive form | rel=r_associated | relid=0 | w=32
  1045. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:22q telomere deletion syndrome
    n1=en:leucinosis | n2=en:22q telomere deletion syndrome | rel=r_associated | relid=0 | w=32
  1046. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:5-oxoprolinase deficiency
    n1=en:leucinosis | n2=en:5-oxoprolinase deficiency | rel=r_associated | relid=0 | w=32
  1047. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:abetalipoproteinemia
    n1=en:leucinosis | n2=en:abetalipoproteinemia | rel=r_associated | relid=0 | w=32
  1048. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:achenbach syndrome
    n1=en:leucinosis | n2=en:achenbach syndrome | rel=r_associated | relid=0 | w=32
  1049. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:acrodermatitis enteropathica
    n1=en:leucinosis | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=32
  1050. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:adenylosuccinate lyase deficiency (disorder)
    n1=en:leucinosis | n2=en:adenylosuccinate lyase deficiency (disorder) | rel=r_associated | relid=0 | w=32
  1051. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:al awadi syndrome
    n1=en:leucinosis | n2=en:al awadi syndrome | rel=r_associated | relid=0 | w=32
  1052. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:albright's hereditary osteodystrophy
    n1=en:leucinosis | n2=en:albright's hereditary osteodystrophy | rel=r_associated | relid=0 | w=32
  1053. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:alport syndrome
    n1=en:leucinosis | n2=en:alport syndrome | rel=r_associated | relid=0 | w=32
  1054. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:amaurosis fugax
    n1=en:leucinosis | n2=en:amaurosis fugax | rel=r_associated | relid=0 | w=32
  1055. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:arakawa syndrome ii
    n1=en:leucinosis | n2=en:arakawa syndrome ii | rel=r_associated | relid=0 | w=32
  1056. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:aspects of radionuclide imaging
    n1=en:leucinosis | n2=en:aspects of radionuclide imaging | rel=r_associated | relid=0 | w=32
  1057. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:autosomal recessive idiopathic familial dystonia
    n1=en:leucinosis | n2=en:autosomal recessive idiopathic familial dystonia | rel=r_associated | relid=0 | w=32
  1058. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:autosomal recessive spastic paraplegia type 11
    n1=en:leucinosis | n2=en:autosomal recessive spastic paraplegia type 11 | rel=r_associated | relid=0 | w=32
  1059. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:becker generalized myotonia
    n1=en:leucinosis | n2=en:becker generalized myotonia | rel=r_associated | relid=0 | w=32
  1060. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:benign neonatal hyperaminoaciduria
    n1=en:leucinosis | n2=en:benign neonatal hyperaminoaciduria | rel=r_associated | relid=0 | w=32
  1061. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:brain diseases, metabolic, inborn
    n1=en:leucinosis | n2=en:brain diseases, metabolic, inborn | rel=r_associated | relid=0 | w=32
  1062. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:carbohydrate-deficient glycoprotein syndrome
    n1=en:leucinosis | n2=en:carbohydrate-deficient glycoprotein syndrome | rel=r_associated | relid=0 | w=32
  1063. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:carney complex
    n1=en:leucinosis | n2=en:carney complex | rel=r_associated | relid=0 | w=32
  1064. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:carnitine palmitoyltransferase i deficiency
    n1=en:leucinosis | n2=en:carnitine palmitoyltransferase i deficiency | rel=r_associated | relid=0 | w=32
  1065. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:caroli disease
    n1=en:leucinosis | n2=en:caroli disease | rel=r_associated | relid=0 | w=32
  1066. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:cartilage hair hypoplasia
    n1=en:leucinosis | n2=en:cartilage hair hypoplasia | rel=r_associated | relid=0 | w=32
  1067. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:cerebral edema
    n1=en:leucinosis | n2=en:cerebral edema | rel=r_associated | relid=0 | w=32
  1068. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:cerebroretinal microangiopathy with calcifications and cysts (disorder)
    n1=en:leucinosis | n2=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | rel=r_associated | relid=0 | w=32
  1069. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:charge syndrome
    n1=en:leucinosis | n2=en:charge syndrome | rel=r_associated | relid=0 | w=32
  1070. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:classical phenylketonuria
    n1=en:leucinosis | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=32
  1071. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:complex regional pain syndrome i
    n1=en:leucinosis | n2=en:complex regional pain syndrome i | rel=r_associated | relid=0 | w=32
  1072. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:conditions tested for in this newborn screening study:id:pt:bld.dot:nom
    n1=en:leucinosis | n2=en:conditions tested for in this newborn screening study:id:pt:bld.dot:nom | rel=r_associated | relid=0 | w=32
  1073. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:congenital disorder of natural immunity
    n1=en:leucinosis | n2=en:congenital disorder of natural immunity | rel=r_associated | relid=0 | w=32
  1074. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:congenital dyserythropoietic anemia, type i
    n1=en:leucinosis | n2=en:congenital dyserythropoietic anemia, type i | rel=r_associated | relid=0 | w=32
  1075. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:congenital ichthyosis
    n1=en:leucinosis | n2=en:congenital ichthyosis | rel=r_associated | relid=0 | w=32
  1076. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
    n1=en:leucinosis | n2=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | rel=r_associated | relid=0 | w=32
  1077. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:congenital pancreatic enterokinase deficiency
    n1=en:leucinosis | n2=en:congenital pancreatic enterokinase deficiency | rel=r_associated | relid=0 | w=32
  1078. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:congenital plasminogen activator inhibitor deficiency type 1
    n1=en:leucinosis | n2=en:congenital plasminogen activator inhibitor deficiency type 1 | rel=r_associated | relid=0 | w=32
  1079. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:costello syndrome
    n1=en:leucinosis | n2=en:costello syndrome | rel=r_associated | relid=0 | w=32
  1080. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:craniodiaphyseal dysplasia
    n1=en:leucinosis | n2=en:craniodiaphyseal dysplasia | rel=r_associated | relid=0 | w=32
  1081. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:dandy-walker malformation
    n1=en:leucinosis | n2=en:dandy-walker malformation | rel=r_associated | relid=0 | w=32
  1082. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:de sanctis-cacchione syndrome
    n1=en:leucinosis | n2=en:de sanctis-cacchione syndrome | rel=r_associated | relid=0 | w=32
  1083. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:defect in post-translational modification of lysosomal enzymes
    n1=en:leucinosis | n2=en:defect in post-translational modification of lysosomal enzymes | rel=r_associated | relid=0 | w=32
  1084. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:deletion 18q syndrome
    n1=en:leucinosis | n2=en:deletion 18q syndrome | rel=r_associated | relid=0 | w=32
  1085. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:developmental hereditary disorder
    n1=en:leucinosis | n2=en:developmental hereditary disorder | rel=r_associated | relid=0 | w=32
  1086. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:ectodermal dysplasia
    n1=en:leucinosis | n2=en:ectodermal dysplasia | rel=r_associated | relid=0 | w=32
  1087. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:epidermolysis bullosa simplex with pyloric atresia
    n1=en:leucinosis | n2=en:epidermolysis bullosa simplex with pyloric atresia | rel=r_associated | relid=0 | w=32
  1088. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:episodic pain syndrome, familial, 3
    n1=en:leucinosis | n2=en:episodic pain syndrome, familial, 3 | rel=r_associated | relid=0 | w=32
  1089. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:familial acantholysis
    n1=en:leucinosis | n2=en:familial acantholysis | rel=r_associated | relid=0 | w=32
  1090. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:familial chronic lymphocytic leukemia
    n1=en:leucinosis | n2=en:familial chronic lymphocytic leukemia | rel=r_associated | relid=0 | w=32
  1091. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:familial hypertrophic cardiomyopathy
    n1=en:leucinosis | n2=en:familial hypertrophic cardiomyopathy | rel=r_associated | relid=0 | w=32
  1092. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:familial neuroblastoma
    n1=en:leucinosis | n2=en:familial neuroblastoma | rel=r_associated | relid=0 | w=32
  1093. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:familial periodic paralysis
    n1=en:leucinosis | n2=en:familial periodic paralysis | rel=r_associated | relid=0 | w=32
  1094. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:familial waldenstrom macroglobulinemia
    n1=en:leucinosis | n2=en:familial waldenstrom macroglobulinemia | rel=r_associated | relid=0 | w=32
  1095. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:gangrenous stomatitis
    n1=en:leucinosis | n2=en:gangrenous stomatitis | rel=r_associated | relid=0 | w=32
  1096. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:gaucher disease
    n1=en:leucinosis | n2=en:gaucher disease | rel=r_associated | relid=0 | w=32
  1097. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:glutamate formiminotransferase deficiency
    n1=en:leucinosis | n2=en:glutamate formiminotransferase deficiency | rel=r_associated | relid=0 | w=32
  1098. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:glutaric acidemia type 1
    n1=en:leucinosis | n2=en:glutaric acidemia type 1 | rel=r_associated | relid=0 | w=32
  1099. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:granular corneal dystrophy
    n1=en:leucinosis | n2=en:granular corneal dystrophy | rel=r_associated | relid=0 | w=32
  1100. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:hantavirus pulmonary syndrome
    n1=en:leucinosis | n2=en:hantavirus pulmonary syndrome | rel=r_associated | relid=0 | w=32
  1101. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:harrod doman keele syndrome
    n1=en:leucinosis | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  1102. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:hemoglobinopathy
    n1=en:leucinosis | n2=en:hemoglobinopathy | rel=r_associated | relid=0 | w=32
  1103. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:hemolytic anemia due to pyruvate kinase deficiency
    n1=en:leucinosis | n2=en:hemolytic anemia due to pyruvate kinase deficiency | rel=r_associated | relid=0 | w=32
  1104. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:hepatolenticular degeneration
    n1=en:leucinosis | n2=en:hepatolenticular degeneration | rel=r_associated | relid=0 | w=32
  1105. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:hereditary breast and ovarian cancer syndrome
    n1=en:leucinosis | n2=en:hereditary breast and ovarian cancer syndrome | rel=r_associated | relid=0 | w=32
  1106. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:hereditary hypoplasminogenemia
    n1=en:leucinosis | n2=en:hereditary hypoplasminogenemia | rel=r_associated | relid=0 | w=32
  1107. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:hereditary multiple exostoses
    n1=en:leucinosis | n2=en:hereditary multiple exostoses | rel=r_associated | relid=0 | w=32
  1108. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:hereditary pancreatitis
    n1=en:leucinosis | n2=en:hereditary pancreatitis | rel=r_associated | relid=0 | w=32
  1109. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:hnsha due to diphosphoglycerate mutase deficiency
    n1=en:leucinosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32
  1110. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:hyperimmunoglobulin e syndrome
    n1=en:leucinosis | n2=en:hyperimmunoglobulin e syndrome | rel=r_associated | relid=0 | w=32
  1111. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:hypoalphalipoproteinemia
    n1=en:leucinosis | n2=en:hypoalphalipoproteinemia | rel=r_associated | relid=0 | w=32
  1112. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:hypohidrotic ectodermal dysplasia with immune deficiency
    n1=en:leucinosis | n2=en:hypohidrotic ectodermal dysplasia with immune deficiency | rel=r_associated | relid=0 | w=32
  1113. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:hypokalemic periodic paralysis
    n1=en:leucinosis | n2=en:hypokalemic periodic paralysis | rel=r_associated | relid=0 | w=32
  1114. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:hypophosphatasia
    n1=en:leucinosis | n2=en:hypophosphatasia | rel=r_associated | relid=0 | w=32
  1115. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:inherited aminoaciduria
    n1=en:leucinosis | n2=en:inherited aminoaciduria | rel=r_associated | relid=0 | w=32
  1116. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:inherited disorder of thyroid metabolism
    n1=en:leucinosis | n2=en:inherited disorder of thyroid metabolism | rel=r_associated | relid=0 | w=32
  1117. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:jervell and lange nielsen syndrome
    n1=en:leucinosis | n2=en:jervell and lange nielsen syndrome | rel=r_associated | relid=0 | w=32
  1118. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:kallmann syndrome
    n1=en:leucinosis | n2=en:kallmann syndrome | rel=r_associated | relid=0 | w=32
  1119. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:klinefelter syndrome
    n1=en:leucinosis | n2=en:klinefelter syndrome | rel=r_associated | relid=0 | w=32
  1120. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:kluver-bucy syndrome
    n1=en:leucinosis | n2=en:kluver-bucy syndrome | rel=r_associated | relid=0 | w=32
  1121. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:kuskokwim disease
    n1=en:leucinosis | n2=en:kuskokwim disease | rel=r_associated | relid=0 | w=32
  1122. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:lactose intolerance, adult type
    n1=en:leucinosis | n2=en:lactose intolerance, adult type | rel=r_associated | relid=0 | w=32
  1123. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:lipoprotein glomerulopathy
    n1=en:leucinosis | n2=en:lipoprotein glomerulopathy | rel=r_associated | relid=0 | w=32
  1124. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:melkersson-rosenthal syndrome
    n1=en:leucinosis | n2=en:melkersson-rosenthal syndrome | rel=r_associated | relid=0 | w=32
  1125. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:metabolic disorder being monitored:prid:pt:bld.dot:nom
    n1=en:leucinosis | n2=en:metabolic disorder being monitored:prid:pt:bld.dot:nom | rel=r_associated | relid=0 | w=32
  1126. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:methylmalonic acidemia
    n1=en:leucinosis | n2=en:methylmalonic acidemia | rel=r_associated | relid=0 | w=32
  1127. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:microcephaly cervical spine fusion anomalies
    n1=en:leucinosis | n2=en:microcephaly cervical spine fusion anomalies | rel=r_associated | relid=0 | w=32
  1128. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:microcephaly, amish type (disorder)
    n1=en:leucinosis | n2=en:microcephaly, amish type (disorder) | rel=r_associated | relid=0 | w=32
  1129. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:mmih syndrome
    n1=en:leucinosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
  1130. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:mobius syndrome
    n1=en:leucinosis | n2=en:mobius syndrome | rel=r_associated | relid=0 | w=32
  1131. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:monilethrix
    n1=en:leucinosis | n2=en:monilethrix | rel=r_associated | relid=0 | w=32
  1132. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:moyamoya disease
    n1=en:leucinosis | n2=en:moyamoya disease | rel=r_associated | relid=0 | w=32
  1133. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:multiple endocrine neoplasia type 2a
    n1=en:leucinosis | n2=en:multiple endocrine neoplasia type 2a | rel=r_associated | relid=0 | w=32
  1134. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:netherton syndrome
    n1=en:leucinosis | n2=en:netherton syndrome | rel=r_associated | relid=0 | w=32
  1135. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:neuronal ceroid lipofuscinosis
    n1=en:leucinosis | n2=en:neuronal ceroid lipofuscinosis | rel=r_associated | relid=0 | w=32
  1136. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:neutral lipid storage disease with myopathy
    n1=en:leucinosis | n2=en:neutral lipid storage disease with myopathy | rel=r_associated | relid=0 | w=32
  1137. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:ornithine carbamoyltransferase deficiency disease
    n1=en:leucinosis | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=32
  1138. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:orofacial cleft 1
    n1=en:leucinosis | n2=en:orofacial cleft 1 | rel=r_associated | relid=0 | w=32
  1139. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:osteopoikilosis
    n1=en:leucinosis | n2=en:osteopoikilosis | rel=r_associated | relid=0 | w=32
  1140. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:pancreatic alpha-amylase deficiency
    n1=en:leucinosis | n2=en:pancreatic alpha-amylase deficiency | rel=r_associated | relid=0 | w=32
  1141. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:paragonimiasis
    n1=en:leucinosis | n2=en:paragonimiasis | rel=r_associated | relid=0 | w=32
  1142. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:piebaldism
    n1=en:leucinosis | n2=en:piebaldism | rel=r_associated | relid=0 | w=32
  1143. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:plague
    n1=en:leucinosis | n2=en:plague | rel=r_associated | relid=0 | w=32
  1144. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:polygenic hereditary disorder
    n1=en:leucinosis | n2=en:polygenic hereditary disorder | rel=r_associated | relid=0 | w=32
  1145. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:porphobilinogen synthase deficiency
    n1=en:leucinosis | n2=en:porphobilinogen synthase deficiency | rel=r_associated | relid=0 | w=32
  1146. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:postaxial polydactyly type a
    n1=en:leucinosis | n2=en:postaxial polydactyly type a | rel=r_associated | relid=0 | w=32
  1147. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:progressive supranuclear palsy
    n1=en:leucinosis | n2=en:progressive supranuclear palsy | rel=r_associated | relid=0 | w=32
  1148. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:pseudoachondroplasia
    n1=en:leucinosis | n2=en:pseudoachondroplasia | rel=r_associated | relid=0 | w=32
  1149. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:pseudohypoaldosteronism, type 1, recessive form
    n1=en:leucinosis | n2=en:pseudohypoaldosteronism, type 1, recessive form | rel=r_associated | relid=0 | w=32
  1150. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:pseudoxanthoma elasticum
    n1=en:leucinosis | n2=en:pseudoxanthoma elasticum | rel=r_associated | relid=0 | w=32
  1151. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:pyruvate dehydrogenase deficiency
    n1=en:leucinosis | n2=en:pyruvate dehydrogenase deficiency | rel=r_associated | relid=0 | w=32
  1152. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:renal tubular transport, inborn errors
    n1=en:leucinosis | n2=en:renal tubular transport, inborn errors | rel=r_associated | relid=0 | w=32
  1153. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:retinoblastoma
    n1=en:leucinosis | n2=en:retinoblastoma | rel=r_associated | relid=0 | w=32
  1154. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:rett syndrome
    n1=en:leucinosis | n2=en:rett syndrome | rel=r_associated | relid=0 | w=32
  1155. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:roberts syndrome
    n1=en:leucinosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  1156. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:schinzel-giedion midface-retraction syndrome
    n1=en:leucinosis | n2=en:schinzel-giedion midface-retraction syndrome | rel=r_associated | relid=0 | w=32
  1157. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:selective antibody deficiency with normal immunoglobulins
    n1=en:leucinosis | n2=en:selective antibody deficiency with normal immunoglobulins | rel=r_associated | relid=0 | w=32
  1158. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:spinal muscular atrophy
    n1=en:leucinosis | n2=en:spinal muscular atrophy | rel=r_associated | relid=0 | w=32
  1159. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:spinocerebellar ataxia with epilepsy
    n1=en:leucinosis | n2=en:spinocerebellar ataxia with epilepsy | rel=r_associated | relid=0 | w=32
  1160. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:spinocerebellar ataxia, autosomal recessive 2
    n1=en:leucinosis | n2=en:spinocerebellar ataxia, autosomal recessive 2 | rel=r_associated | relid=0 | w=32
  1161. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:spondylo-ocular syndrome
    n1=en:leucinosis | n2=en:spondylo-ocular syndrome | rel=r_associated | relid=0 | w=32
  1162. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:spondyloepimetaphyseal dysplasia, sponastrime type
    n1=en:leucinosis | n2=en:spondyloepimetaphyseal dysplasia, sponastrime type | rel=r_associated | relid=0 | w=32
  1163. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:spondyloepiphyseal dysplasia tarda, toledo type
    n1=en:leucinosis | n2=en:spondyloepiphyseal dysplasia tarda, toledo type | rel=r_associated | relid=0 | w=32
  1164. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:steroid metabolism, inborn errors
    n1=en:leucinosis | n2=en:steroid metabolism, inborn errors | rel=r_associated | relid=0 | w=32
  1165. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:storage disease
    n1=en:leucinosis | n2=en:storage disease | rel=r_associated | relid=0 | w=32
  1166. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:tetra-amelia autosomal recessive
    n1=en:leucinosis | n2=en:tetra-amelia autosomal recessive | rel=r_associated | relid=0 | w=32
  1167. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:thomas syndrome
    n1=en:leucinosis | n2=en:thomas syndrome | rel=r_associated | relid=0 | w=32
  1168. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:tuberous sclerosis
    n1=en:leucinosis | n2=en:tuberous sclerosis | rel=r_associated | relid=0 | w=32
  1169. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:waardenburg anophthalmia syndrome
    n1=en:leucinosis | n2=en:waardenburg anophthalmia syndrome | rel=r_associated | relid=0 | w=32
  1170. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:warsaw breakage syndrome
    n1=en:leucinosis | n2=en:warsaw breakage syndrome | rel=r_associated | relid=0 | w=32
  1171. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:wolfram syndrome
    n1=en:leucinosis | n2=en:wolfram syndrome | rel=r_associated | relid=0 | w=32
  1172. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:worldwide incidence of 1 in 185,000 live births
    n1=en:leucinosis | n2=en:worldwide incidence of 1 in 185,000 live births | rel=r_associated | relid=0 | w=32
  1173. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:wt limb blood syndrome
    n1=en:leucinosis | n2=en:wt limb blood syndrome | rel=r_associated | relid=0 | w=32
  1174. en:leucinosis -- r_associated #0: 32 / 0.615 -> en:zellweger syndrome
    n1=en:leucinosis | n2=en:zellweger syndrome | rel=r_associated | relid=0 | w=32
  1175. en:leucinosis -- r_associated #0: 32 / 0.615 -> maladie génétique
    n1=en:leucinosis | n2=maladie génétique | rel=r_associated | relid=0 | w=32
  1176. en:leucinosis -- r_associated #0: 32 / 0.615 -> sirop
    n1=en:leucinosis | n2=sirop | rel=r_associated | relid=0 | w=32
  1177. en:leucinosis -- r_associated #0: 31 / 0.596 -> affection
    n1=en:leucinosis | n2=affection | rel=r_associated | relid=0 | w=31
  1178. en:leucinosis -- r_associated #0: 31 / 0.596 -> BCKBB gene
    n1=en:leucinosis | n2=BCKBB gene | rel=r_associated | relid=0 | w=31
  1179. en:leucinosis -- r_associated #0: 31 / 0.596 -> DBT gene
    n1=en:leucinosis | n2=DBT gene | rel=r_associated | relid=0 | w=31
  1180. en:leucinosis -- r_associated #0: 31 / 0.596 -> déficit en
    n1=en:leucinosis | n2=déficit en | rel=r_associated | relid=0 | w=31
  1181. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:acetyl-coa: carboxylase deficiency
    n1=en:leucinosis | n2=en:acetyl-coa: carboxylase deficiency | rel=r_associated | relid=0 | w=31
  1182. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:acquired lactase deficiency
    n1=en:leucinosis | n2=en:acquired lactase deficiency | rel=r_associated | relid=0 | w=31
  1183. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:acrodermatitis
    n1=en:leucinosis | n2=en:acrodermatitis | rel=r_associated | relid=0 | w=31
  1184. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:acromegaly
    n1=en:leucinosis | n2=en:acromegaly | rel=r_associated | relid=0 | w=31
  1185. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:acute intermittent porphyria
    n1=en:leucinosis | n2=en:acute intermittent porphyria | rel=r_associated | relid=0 | w=31
  1186. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:acyl-coa dehydrogenase deficiency
    n1=en:leucinosis | n2=en:acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=31
  1187. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:albinotic fundus
    n1=en:leucinosis | n2=en:albinotic fundus | rel=r_associated | relid=0 | w=31
  1188. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:alpha-methylacyl-coa racemase deficiency
    n1=en:leucinosis | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=31
  1189. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:amino acidemia disorder suspected:prid:pt:bld.dot:nom
    n1=en:leucinosis | n2=en:amino acidemia disorder suspected:prid:pt:bld.dot:nom | rel=r_associated | relid=0 | w=31
  1190. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:andersen syndrome
    n1=en:leucinosis | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=31
  1191. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:aniridia
    n1=en:leucinosis | n2=en:aniridia | rel=r_associated | relid=0 | w=31
  1192. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:atrophoderma vermiculatum
    n1=en:leucinosis | n2=en:atrophoderma vermiculatum | rel=r_associated | relid=0 | w=31
  1193. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:auditory perceptual disorder
    n1=en:leucinosis | n2=en:auditory perceptual disorder | rel=r_associated | relid=0 | w=31
  1194. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:autoimmune lymphoproliferative syndrome
    n1=en:leucinosis | n2=en:autoimmune lymphoproliferative syndrome | rel=r_associated | relid=0 | w=31
  1195. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:autosomal recessive ocular albinism
    n1=en:leucinosis | n2=en:autosomal recessive ocular albinism | rel=r_associated | relid=0 | w=31
  1196. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:autosomal recessive sideroblastic anemia
    n1=en:leucinosis | n2=en:autosomal recessive sideroblastic anemia | rel=r_associated | relid=0 | w=31
  1197. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:bothnia retinal dystrophy
    n1=en:leucinosis | n2=en:bothnia retinal dystrophy | rel=r_associated | relid=0 | w=31
  1198. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:brody myopathy
    n1=en:leucinosis | n2=en:brody myopathy | rel=r_associated | relid=0 | w=31
  1199. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:cadasil syndrome
    n1=en:leucinosis | n2=en:cadasil syndrome | rel=r_associated | relid=0 | w=31
  1200. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:cataplexy
    n1=en:leucinosis | n2=en:cataplexy | rel=r_associated | relid=0 | w=31
  1201. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:caused by mutation in the dihydrolipoamide branched chain transacylase gene (dbt, 248610.0001)
    n1=en:leucinosis | n2=en:caused by mutation in the dihydrolipoamide branched chain transacylase gene (dbt, 248610.0001) | rel=r_associated | relid=0 | w=31
  1202. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:caused by mutation in the dihydrolipoamide dehydrogenase gene (dld, 238331.0001)
    n1=en:leucinosis | n2=en:caused by mutation in the dihydrolipoamide dehydrogenase gene (dld, 238331.0001) | rel=r_associated | relid=0 | w=31
  1203. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
    n1=en:leucinosis | n2=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | rel=r_associated | relid=0 | w=31
  1204. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:chitty hall baraitser syndrome
    n1=en:leucinosis | n2=en:chitty hall baraitser syndrome | rel=r_associated | relid=0 | w=31
  1205. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:citrin deficiency
    n1=en:leucinosis | n2=en:citrin deficiency | rel=r_associated | relid=0 | w=31
  1206. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:congenital bilateral aplasia of the vas deferens
    n1=en:leucinosis | n2=en:congenital bilateral aplasia of the vas deferens | rel=r_associated | relid=0 | w=31
  1207. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:congenital pure red cell aplasia
    n1=en:leucinosis | n2=en:congenital pure red cell aplasia | rel=r_associated | relid=0 | w=31
  1208. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:corpus callosum agenesis neuronopathy
    n1=en:leucinosis | n2=en:corpus callosum agenesis neuronopathy | rel=r_associated | relid=0 | w=31
  1209. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:craniofacial dysostosis
    n1=en:leucinosis | n2=en:craniofacial dysostosis | rel=r_associated | relid=0 | w=31
  1210. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:crigler-najjar syndrome
    n1=en:leucinosis | n2=en:crigler-najjar syndrome | rel=r_associated | relid=0 | w=31
  1211. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:cutis laxa
    n1=en:leucinosis | n2=en:cutis laxa | rel=r_associated | relid=0 | w=31
  1212. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:cutis laxa, autosomal recessive
    n1=en:leucinosis | n2=en:cutis laxa, autosomal recessive | rel=r_associated | relid=0 | w=31
  1213. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:deficiency of fructokinase
    n1=en:leucinosis | n2=en:deficiency of fructokinase | rel=r_associated | relid=0 | w=31
  1214. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:deficiency of steryl-sulfatase
    n1=en:leucinosis | n2=en:deficiency of steryl-sulfatase | rel=r_associated | relid=0 | w=31
  1215. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:dentinogenesis imperfecta
    n1=en:leucinosis | n2=en:dentinogenesis imperfecta | rel=r_associated | relid=0 | w=31
  1216. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:dihydrouracil dehydrogenase deficiency
    n1=en:leucinosis | n2=en:dihydrouracil dehydrogenase deficiency | rel=r_associated | relid=0 | w=31
  1217. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:disorder of pyruvate metabolism and mitochondrial respiratory chain
    n1=en:leucinosis | n2=en:disorder of pyruvate metabolism and mitochondrial respiratory chain | rel=r_associated | relid=0 | w=31
  1218. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:disorder of sialic acid metabolism
    n1=en:leucinosis | n2=en:disorder of sialic acid metabolism | rel=r_associated | relid=0 | w=31
  1219. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:enzymology
    n1=en:leucinosis | n2=en:enzymology | rel=r_associated | relid=0 | w=31
  1220. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:erythropoietic protoporphyria
    n1=en:leucinosis | n2=en:erythropoietic protoporphyria | rel=r_associated | relid=0 | w=31
  1221. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:familial hypoaldosteronism
    n1=en:leucinosis | n2=en:familial hypoaldosteronism | rel=r_associated | relid=0 | w=31
  1222. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:familial renal iminoglycinuria
    n1=en:leucinosis | n2=en:familial renal iminoglycinuria | rel=r_associated | relid=0 | w=31
  1223. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:feingold syndrome
    n1=en:leucinosis | n2=en:feingold syndrome | rel=r_associated | relid=0 | w=31
  1224. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:fetus with hereditary disease
    n1=en:leucinosis | n2=en:fetus with hereditary disease | rel=r_associated | relid=0 | w=31
  1225. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:fragile x syndrome
    n1=en:leucinosis | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=31
  1226. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:galactosemia
    n1=en:leucinosis | n2=en:galactosemia | rel=r_associated | relid=0 | w=31
  1227. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:gastric antral vascular ectasia
    n1=en:leucinosis | n2=en:gastric antral vascular ectasia | rel=r_associated | relid=0 | w=31
  1228. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:gastroschisis
    n1=en:leucinosis | n2=en:gastroschisis | rel=r_associated | relid=0 | w=31
  1229. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:genetic aspects
    n1=en:leucinosis | n2=en:genetic aspects | rel=r_associated | relid=0 | w=31
  1230. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:giacci familial neurogenic acroosteolysis
    n1=en:leucinosis | n2=en:giacci familial neurogenic acroosteolysis | rel=r_associated | relid=0 | w=31
  1231. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:gitelman syndrome
    n1=en:leucinosis | n2=en:gitelman syndrome | rel=r_associated | relid=0 | w=31
  1232. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:glutathione synthetase deficiency
    n1=en:leucinosis | n2=en:glutathione synthetase deficiency | rel=r_associated | relid=0 | w=31
  1233. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:goodpasture syndrome
    n1=en:leucinosis | n2=en:goodpasture syndrome | rel=r_associated | relid=0 | w=31
  1234. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hartnup disease
    n1=en:leucinosis | n2=en:hartnup disease | rel=r_associated | relid=0 | w=31
  1235. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hemochromatosis
    n1=en:leucinosis | n2=en:hemochromatosis | rel=r_associated | relid=0 | w=31
  1236. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hemophilia b
    n1=en:leucinosis | n2=en:hemophilia b | rel=r_associated | relid=0 | w=31
  1237. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hemorrhagic fever with renal syndrome
    n1=en:leucinosis | n2=en:hemorrhagic fever with renal syndrome | rel=r_associated | relid=0 | w=31
  1238. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hereditary central nervous system demyelinating diseases
    n1=en:leucinosis | n2=en:hereditary central nervous system demyelinating diseases | rel=r_associated | relid=0 | w=31
  1239. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hereditary coproporphyria
    n1=en:leucinosis | n2=en:hereditary coproporphyria | rel=r_associated | relid=0 | w=31
  1240. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hereditary diffuse gastric adenocarcinoma
    n1=en:leucinosis | n2=en:hereditary diffuse gastric adenocarcinoma | rel=r_associated | relid=0 | w=31
  1241. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hereditary disorder by system
    n1=en:leucinosis | n2=en:hereditary disorder by system | rel=r_associated | relid=0 | w=31
  1242. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hereditary methemoglobinemia, enzymatic type
    n1=en:leucinosis | n2=en:hereditary methemoglobinemia, enzymatic type | rel=r_associated | relid=0 | w=31
  1243. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hereditary renal cell cancer
    n1=en:leucinosis | n2=en:hereditary renal cell cancer | rel=r_associated | relid=0 | w=31
  1244. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:homocystinemia
    n1=en:leucinosis | n2=en:homocystinemia | rel=r_associated | relid=0 | w=31
  1245. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hydroxykynureninuria
    n1=en:leucinosis | n2=en:hydroxykynureninuria | rel=r_associated | relid=0 | w=31
  1246. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hyperglycerolemia
    n1=en:leucinosis | n2=en:hyperglycerolemia | rel=r_associated | relid=0 | w=31
  1247. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hyperglycinemia
    n1=en:leucinosis | n2=en:hyperglycinemia | rel=r_associated | relid=0 | w=31
  1248. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hyperhomocysteinemia
    n1=en:leucinosis | n2=en:hyperhomocysteinemia | rel=r_associated | relid=0 | w=31
  1249. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hyperpipecolatemia
    n1=en:leucinosis | n2=en:hyperpipecolatemia | rel=r_associated | relid=0 | w=31
  1250. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:hypomagnesemia 1, intestinal
    n1=en:leucinosis | n2=en:hypomagnesemia 1, intestinal | rel=r_associated | relid=0 | w=31
  1251. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:ichthyosis
    n1=en:leucinosis | n2=en:ichthyosis | rel=r_associated | relid=0 | w=31
  1252. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:intermittent maple syrup urine disease
    n1=en:leucinosis | n2=en:intermittent maple syrup urine disease | rel=r_associated | relid=0 | w=31
  1253. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:isovaleric acidemia
    n1=en:leucinosis | n2=en:isovaleric acidemia | rel=r_associated | relid=0 | w=31
  1254. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:juvenile x-linked retinoschisis
    n1=en:leucinosis | n2=en:juvenile x-linked retinoschisis | rel=r_associated | relid=0 | w=31
  1255. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:kearns-sayre syndrome
    n1=en:leucinosis | n2=en:kearns-sayre syndrome | rel=r_associated | relid=0 | w=31
  1256. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:lactase deficiency, congenital
    n1=en:leucinosis | n2=en:lactase deficiency, congenital | rel=r_associated | relid=0 | w=31
  1257. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:levocardia
    n1=en:leucinosis | n2=en:levocardia | rel=r_associated | relid=0 | w=31
  1258. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:lipoid congenital adrenal hyperplasia
    n1=en:leucinosis | n2=en:lipoid congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=31
  1259. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:malformations of cortical development
    n1=en:leucinosis | n2=en:malformations of cortical development | rel=r_associated | relid=0 | w=31
  1260. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:maple syrup urine disease, type 1a
    n1=en:leucinosis | n2=en:maple syrup urine disease, type 1a | rel=r_associated | relid=0 | w=31
  1261. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:mcdonough syndrome
    n1=en:leucinosis | n2=en:mcdonough syndrome | rel=r_associated | relid=0 | w=31
  1262. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:megalencephalic leukoencephalopathy with subcortical cysts
    n1=en:leucinosis | n2=en:megalencephalic leukoencephalopathy with subcortical cysts | rel=r_associated | relid=0 | w=31
  1263. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:mendelian disorders
    n1=en:leucinosis | n2=en:mendelian disorders | rel=r_associated | relid=0 | w=31
  1264. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency
    n1=en:leucinosis | n2=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | rel=r_associated | relid=0 | w=31
  1265. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:mental retardation if untreated
    n1=en:leucinosis | n2=en:mental retardation if untreated | rel=r_associated | relid=0 | w=31
  1266. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:methionine adenosyltransferase deficiency
    n1=en:leucinosis | n2=en:methionine adenosyltransferase deficiency | rel=r_associated | relid=0 | w=31
  1267. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:mevalonate kinase deficiency
    n1=en:leucinosis | n2=en:mevalonate kinase deficiency | rel=r_associated | relid=0 | w=31
  1268. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:microcephaly-capillary malformation syndrome
    n1=en:leucinosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  1269. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:migrating partial seizures in infancy
    n1=en:leucinosis | n2=en:migrating partial seizures in infancy | rel=r_associated | relid=0 | w=31
  1270. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:miller-mckusick-malvaux-syndrome (3m syndrome)
    n1=en:leucinosis | n2=en:miller-mckusick-malvaux-syndrome (3m syndrome) | rel=r_associated | relid=0 | w=31
  1271. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:mitochondrial dna depletion syndrome 2 (myopathic type)
    n1=en:leucinosis | n2=en:mitochondrial dna depletion syndrome 2 (myopathic type) | rel=r_associated | relid=0 | w=31
  1272. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:molybdenum cofactor deficiency
    n1=en:leucinosis | n2=en:molybdenum cofactor deficiency | rel=r_associated | relid=0 | w=31
  1273. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:multiple carboxylase deficiency
    n1=en:leucinosis | n2=en:multiple carboxylase deficiency | rel=r_associated | relid=0 | w=31
  1274. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:muscle amp deaminase deficiency
    n1=en:leucinosis | n2=en:muscle amp deaminase deficiency | rel=r_associated | relid=0 | w=31
  1275. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:muscle d-lactate dehydrogenase deficiency
    n1=en:leucinosis | n2=en:muscle d-lactate dehydrogenase deficiency | rel=r_associated | relid=0 | w=31
  1276. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:muscle-eye-brain disease, congenital muscular dystrophy
    n1=en:leucinosis | n2=en:muscle-eye-brain disease, congenital muscular dystrophy | rel=r_associated | relid=0 | w=31
  1277. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:nathalie syndrome
    n1=en:leucinosis | n2=en:nathalie syndrome | rel=r_associated | relid=0 | w=31
  1278. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:neonatal research network terminology
    n1=en:leucinosis | n2=en:neonatal research network terminology | rel=r_associated | relid=0 | w=31
  1279. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:neurocysticercosis
    n1=en:leucinosis | n2=en:neurocysticercosis | rel=r_associated | relid=0 | w=31
  1280. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:neurofibromatosis type 1
    n1=en:leucinosis | n2=en:neurofibromatosis type 1 | rel=r_associated | relid=0 | w=31
  1281. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:neuropathy, hereditary sensory and autonomic, type vii
    n1=en:leucinosis | n2=en:neuropathy, hereditary sensory and autonomic, type vii | rel=r_associated | relid=0 | w=31
  1282. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:nursing therapy
    n1=en:leucinosis | n2=en:nursing therapy | rel=r_associated | relid=0 | w=31
  1283. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:osteogenesis imperfecta
    n1=en:leucinosis | n2=en:osteogenesis imperfecta | rel=r_associated | relid=0 | w=31
  1284. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:other disturbances of straight-chain amino-acid metabolism
    n1=en:leucinosis | n2=en:other disturbances of straight-chain amino-acid metabolism | rel=r_associated | relid=0 | w=31
  1285. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:pallister-hall syndrome
    n1=en:leucinosis | n2=en:pallister-hall syndrome | rel=r_associated | relid=0 | w=31
  1286. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:parasitology
    n1=en:leucinosis | n2=en:parasitology | rel=r_associated | relid=0 | w=31
  1287. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:pearson marrow-pancreas syndrome
    n1=en:leucinosis | n2=en:pearson marrow-pancreas syndrome | rel=r_associated | relid=0 | w=31
  1288. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:pick's disease
    n1=en:leucinosis | n2=en:pick's disease | rel=r_associated | relid=0 | w=31
  1289. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:pinta
    n1=en:leucinosis | n2=en:pinta | rel=r_associated | relid=0 | w=31
  1290. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:popliteal pterygium syndrome
    n1=en:leucinosis | n2=en:popliteal pterygium syndrome | rel=r_associated | relid=0 | w=31
  1291. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:potocki-lupski syndrome
    n1=en:leucinosis | n2=en:potocki-lupski syndrome | rel=r_associated | relid=0 | w=31
  1292. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:prekallikrein deficiency
    n1=en:leucinosis | n2=en:prekallikrein deficiency | rel=r_associated | relid=0 | w=31
  1293. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:progressive muscular atrophy
    n1=en:leucinosis | n2=en:progressive muscular atrophy | rel=r_associated | relid=0 | w=31
  1294. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:pseudotrisomy 13 syndrome
    n1=en:leucinosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  1295. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:pulmonary alveolar proteinosis
    n1=en:leucinosis | n2=en:pulmonary alveolar proteinosis | rel=r_associated | relid=0 | w=31
  1296. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:purine-nucleoside phosphorylase deficiency
    n1=en:leucinosis | n2=en:purine-nucleoside phosphorylase deficiency | rel=r_associated | relid=0 | w=31
  1297. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:roentgenographic
    n1=en:leucinosis | n2=en:roentgenographic | rel=r_associated | relid=0 | w=31
  1298. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:scimitar syndrome
    n1=en:leucinosis | n2=en:scimitar syndrome | rel=r_associated | relid=0 | w=31
  1299. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:sea-blue histiocyte syndrome
    n1=en:leucinosis | n2=en:sea-blue histiocyte syndrome | rel=r_associated | relid=0 | w=31
  1300. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:severe mental retardation (i.q. 20-34)
    n1=en:leucinosis | n2=en:severe mental retardation (i.q. 20-34) | rel=r_associated | relid=0 | w=31
  1301. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:severe steroid 21-hydroxylase deficiency
    n1=en:leucinosis | n2=en:severe steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=31
  1302. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:short rib-polydactyly syndrome
    n1=en:leucinosis | n2=en:short rib-polydactyly syndrome | rel=r_associated | relid=0 | w=31
  1303. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:sitosterolemia with xanthomatosis
    n1=en:leucinosis | n2=en:sitosterolemia with xanthomatosis | rel=r_associated | relid=0 | w=31
  1304. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:sly syndrome
    n1=en:leucinosis | n2=en:sly syndrome | rel=r_associated | relid=0 | w=31
  1305. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:succinic semialdehyde dehydrogenase deficiency
    n1=en:leucinosis | n2=en:succinic semialdehyde dehydrogenase deficiency | rel=r_associated | relid=0 | w=31
  1306. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:syringomyelia
    n1=en:leucinosis | n2=en:syringomyelia | rel=r_associated | relid=0 | w=31
  1307. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:tyrosinemia type ii
    n1=en:leucinosis | n2=en:tyrosinemia type ii | rel=r_associated | relid=0 | w=31
  1308. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:ugt1a1*28 polymorphism
    n1=en:leucinosis | n2=en:ugt1a1*28 polymorphism | rel=r_associated | relid=0 | w=31
  1309. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:unclassified metabolic disorder
    n1=en:leucinosis | n2=en:unclassified metabolic disorder | rel=r_associated | relid=0 | w=31
  1310. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:urea cycle metabolism disorder
    n1=en:leucinosis | n2=en:urea cycle metabolism disorder | rel=r_associated | relid=0 | w=31
  1311. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:urocanase deficiency
    n1=en:leucinosis | n2=en:urocanase deficiency | rel=r_associated | relid=0 | w=31
  1312. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:vomiting
    n1=en:leucinosis | n2=en:vomiting | rel=r_associated | relid=0 | w=31
  1313. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:wandering spleen
    n1=en:leucinosis | n2=en:wandering spleen | rel=r_associated | relid=0 | w=31
  1314. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:waterhouse-friderichsen syndrome
    n1=en:leucinosis | n2=en:waterhouse-friderichsen syndrome | rel=r_associated | relid=0 | w=31
  1315. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:werner syndrome
    n1=en:leucinosis | n2=en:werner syndrome | rel=r_associated | relid=0 | w=31
  1316. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:wolman disease
    n1=en:leucinosis | n2=en:wolman disease | rel=r_associated | relid=0 | w=31
  1317. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:x-linked bulbar-muscular atrophy
    n1=en:leucinosis | n2=en:x-linked bulbar-muscular atrophy | rel=r_associated | relid=0 | w=31
  1318. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:x-linked hypophosphatemic rickets
    n1=en:leucinosis | n2=en:x-linked hypophosphatemic rickets | rel=r_associated | relid=0 | w=31
  1319. en:leucinosis -- r_associated #0: 31 / 0.596 -> en:x-linked inherited disorder
    n1=en:leucinosis | n2=en:x-linked inherited disorder | rel=r_associated | relid=0 | w=31
  1320. en:leucinosis -- r_associated #0: 31 / 0.596 -> maladie
    (médecine)
    n1=en:leucinosis | n2=maladie
    (médecine)
    | rel=r_associated | relid=0 | w=31
  1321. en:leucinosis -- r_associated #0: 31 / 0.596 -> maladie
    (médecine, vétérinaire)
    n1=en:leucinosis | n2=maladie
    (médecine, vétérinaire)
    | rel=r_associated | relid=0 | w=31
  1322. en:leucinosis -- r_associated #0: 31 / 0.596 -> sirop d'érable
    n1=en:leucinosis | n2=sirop d'érable | rel=r_associated | relid=0 | w=31
  1323. en:leucinosis -- r_associated #0: 30 / 0.577 -> en:hypertonia
    n1=en:leucinosis | n2=en:hypertonia | rel=r_associated | relid=0 | w=30
  1324. en:leucinosis -- r_associated #0: 30 / 0.577 -> en:mild mental retardation
    n1=en:leucinosis | n2=en:mild mental retardation | rel=r_associated | relid=0 | w=30
  1325. en:leucinosis -- r_associated #0: 30 / 0.577 -> en:osteopetrosis with renal tubular acidosis
    n1=en:leucinosis | n2=en:osteopetrosis with renal tubular acidosis | rel=r_associated | relid=0 | w=30
  1326. en:leucinosis -- r_associated #0: 30 / 0.577 -> leucinose
    n1=en:leucinosis | n2=leucinose | rel=r_associated | relid=0 | w=30
  1327. en:leucinosis -- r_associated #0: 30 / 0.577 -> maladie des urines à odeur de sirop d'érable, forme classique
    n1=en:leucinosis | n2=maladie des urines à odeur de sirop d'érable, forme classique | rel=r_associated | relid=0 | w=30
  1328. en:leucinosis -- r_associated #0: 30 / 0.577 -> pathologie
    n1=en:leucinosis | n2=pathologie | rel=r_associated | relid=0 | w=30
  1329. en:leucinosis -- r_associated #0: 30 / 0.577 -> sisi-test
    n1=en:leucinosis | n2=sisi-test | rel=r_associated | relid=0 | w=30
  1330. en:leucinosis -- r_associated #0: 27 / 0.519 -> sismothérapie
    n1=en:leucinosis | n2=sismothérapie | rel=r_associated | relid=0 | w=27
  1331. en:leucinosis -- r_associated #0: 25 / 0.481 -> maladie des urines à odeur de sirop d'érable, forme intermittente
    n1=en:leucinosis | n2=maladie des urines à odeur de sirop d'érable, forme intermittente | rel=r_associated | relid=0 | w=25
  1332. en:leucinosis -- r_associated #0: 25 / 0.481 -> SIRS
    n1=en:leucinosis | n2=SIRS | rel=r_associated | relid=0 | w=25
  1333. en:leucinosis -- r_associated #0: 25 / 0.481 -> sirtuine
    n1=en:leucinosis | n2=sirtuine | rel=r_associated | relid=0 | w=25
  1334. en:leucinosis -- r_associated #0: 24 / 0.462 -> cétoacidurie ramifiée, forme intermittente
    n1=en:leucinosis | n2=cétoacidurie ramifiée, forme intermittente | rel=r_associated | relid=0 | w=24
  1335. en:leucinosis -- r_associated #0: 23 / 0.442 -> SIRT
    n1=en:leucinosis | n2=SIRT | rel=r_associated | relid=0 | w=23
  1336. en:leucinosis -- r_associated #0: 15 / 0.288 -> en:biochemics
    n1=en:leucinosis | n2=en:biochemics | rel=r_associated | relid=0 | w=15
  1337. en:leucinosis -- r_associated #0: 15 / 0.288 -> en:biochemistry
    n1=en:leucinosis | n2=en:biochemistry | rel=r_associated | relid=0 | w=15
  1338. en:leucinosis -- r_associated #0: 10 / 0.192 -> atrophie
    n1=en:leucinosis | n2=atrophie | rel=r_associated | relid=0 | w=10
  1339. en:leucinosis -- r_associated #0: 10 / 0.192 -> en:classical
    n1=en:leucinosis | n2=en:classical | rel=r_associated | relid=0 | w=10
  1340. en:leucinosis -- r_associated #0: 10 / 0.192 -> en:maple
    n1=en:leucinosis | n2=en:maple | rel=r_associated | relid=0 | w=10
  1341. en:leucinosis -- r_associated #0: 10 / 0.192 -> enzyme
    n1=en:leucinosis | n2=enzyme | rel=r_associated | relid=0 | w=10
≈ 1577 relations entrantes

  1. déficit en céto-acide décarboxylase --- r_associated #0: 139 --> en:leucinosis
    n1=déficit en céto-acide décarboxylase | n2=en:leucinosis | rel=r_associated | relid=0 | w=139
  2. en:maple syrup urine disease --- r_associated #0: 135 --> en:leucinosis
    n1=en:maple syrup urine disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=135
  3. en:classical maple syrup urine disease --- r_associated #0: 131 --> en:leucinosis
    n1=en:classical maple syrup urine disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=131
  4. leucinose --- r_associated #0: 131 --> en:leucinosis
    n1=leucinose | n2=en:leucinosis | rel=r_associated | relid=0 | w=131
  5. maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 127 --> en:leucinosis
    n1=maladie des urines à l'odeur de sirop d'érable | n2=en:leucinosis | rel=r_associated | relid=0 | w=127
  6. en:thiamin-responsive maple syrup urine disease --- r_associated #0: 122 --> en:leucinosis
    n1=en:thiamin-responsive maple syrup urine disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=122
  7. maladie des urines avec odeur de sirop erable --- r_associated #0: 112 --> en:leucinosis
    n1=maladie des urines avec odeur de sirop erable | n2=en:leucinosis | rel=r_associated | relid=0 | w=112
  8. maladie du sirop d'érable --- r_associated #0: 110 --> en:leucinosis
    n1=maladie du sirop d'érable | n2=en:leucinosis | rel=r_associated | relid=0 | w=110
  9. sirop d'érable (urine à odeur de) --- r_associated #0: 50 --> en:leucinosis
    n1=sirop d'érable (urine à odeur de) | n2=en:leucinosis | rel=r_associated | relid=0 | w=50
  10. en:maple-tree syrup disease --- r_associated #0: 36 --> en:leucinosis
    n1=en:maple-tree syrup disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=36
  11. anémie à cellules falciformes --- r_associated #0: 35 --> en:leucinosis
    n1=anémie à cellules falciformes | n2=en:leucinosis | rel=r_associated | relid=0 | w=35
  12. bêta-thalassémie à hématies falciformes --- r_associated #0: 30 --> en:leucinosis
    n1=bêta-thalassémie à hématies falciformes | n2=en:leucinosis | rel=r_associated | relid=0 | w=30
  13. maladie des hématies falciformes --- r_associated #0: 30 --> en:leucinosis
    n1=maladie des hématies falciformes | n2=en:leucinosis | rel=r_associated | relid=0 | w=30
  14. en:branched-chain ketoaciduria --- r_associated #0: 28 --> en:leucinosis
    n1=en:branched-chain ketoaciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=28
  15. cétoacidurie à chaînes ramifiées --- r_associated #0: 26 --> en:leucinosis
    n1=cétoacidurie à chaînes ramifiées | n2=en:leucinosis | rel=r_associated | relid=0 | w=26
  16. examen non précisé, méningite tuberculeuse --- r_associated #0: 25 --> en:leucinosis
    n1=examen non précisé, méningite tuberculeuse | n2=en:leucinosis | rel=r_associated | relid=0 | w=25
  17. BCKBB gene --- r_associated #0: 20 --> en:leucinosis
    n1=BCKBB gene | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  18. BCKDHA gene l.angl. pour --- r_associated #0: 20 --> en:leucinosis
    n1=BCKDHA gene l.angl. pour | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  19. Beauvieux (hérédité du syndrome de) --- r_associated #0: 20 --> en:leucinosis
    n1=Beauvieux (hérédité du syndrome de) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  20. DBT gene --- r_associated #0: 20 --> en:leucinosis
    n1=DBT gene | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  21. Hartnup (maladie de) --- r_associated #0: 20 --> en:leucinosis
    n1=Hartnup (maladie de) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  22. Médecine --- r_associated #0: 20 --> en:leucinosis
    n1=Médecine | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  23. acide --- r_associated #0: 20 --> en:leucinosis
    n1=acide | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  24. acide aminé --- r_associated #0: 20 --> en:leucinosis
    n1=acide aminé | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  25. affection --- r_associated #0: 20 --> en:leucinosis
    n1=affection | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  26. anémie drépanocytaire non précisée --- r_associated #0: 20 --> en:leucinosis
    n1=anémie drépanocytaire non précisée | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  27. anémie ss --- r_associated #0: 20 --> en:leucinosis
    n1=anémie ss | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  28. anémie à hématies falciformes --- r_associated #0: 20 --> en:leucinosis
    n1=anémie à hématies falciformes | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  29. biochimie --- r_associated #0: 20 --> en:leucinosis
    n1=biochimie | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  30. cerveau --- r_associated #0: 20 --> en:leucinosis
    n1=cerveau | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  31. cerveau
    (anatomie)
     --- r_associated #0: 20 --> en:leucinosis
    n1=cerveau
    (anatomie)
    | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  32. chromosome --- r_associated #0: 20 --> en:leucinosis
    n1=chromosome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  33. chromosome 19 --- r_associated #0: 20 --> en:leucinosis
    n1=chromosome 19 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  34. chromosome 7 --- r_associated #0: 20 --> en:leucinosis
    n1=chromosome 7 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  35. complexe 3-méthyl-2-oxobutanoate déshydrogénase --- r_associated #0: 20 --> en:leucinosis
    n1=complexe 3-méthyl-2-oxobutanoate déshydrogénase | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  36. congenital --- r_associated #0: 20 --> en:leucinosis
    n1=congenital | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  37. cérumen --- r_associated #0: 20 --> en:leucinosis
    n1=cérumen | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  38. céto --- r_associated #0: 20 --> en:leucinosis
    n1=céto | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  39. cétoacidurie ramifiée --- r_associated #0: 20 --> en:leucinosis
    n1=cétoacidurie ramifiée | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  40. drépanocytose homozygote --- r_associated #0: 20 --> en:leucinosis
    n1=drépanocytose homozygote | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  41. drépanocytoses --- r_associated #0: 20 --> en:leucinosis
    n1=drépanocytoses | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  42. dysplasie olfacto-génitale --- r_associated #0: 20 --> en:leucinosis
    n1=dysplasie olfacto-génitale | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  43. dysplasie olfactogénitale --- r_associated #0: 20 --> en:leucinosis
    n1=dysplasie olfactogénitale | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  44. dysplasie olfactogénitale de De Morsier --- r_associated #0: 20 --> en:leucinosis
    n1=dysplasie olfactogénitale de De Morsier | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  45. décarboxylase --- r_associated #0: 20 --> en:leucinosis
    n1=décarboxylase | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  46. déficit --- r_associated #0: 20 --> en:leucinosis
    n1=déficit | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  47. déficit en --- r_associated #0: 20 --> en:leucinosis
    n1=déficit en | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  48. déficit en alpha-céto-acide déshydrogénase --- r_associated #0: 20 --> en:leucinosis
    n1=déficit en alpha-céto-acide déshydrogénase | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  49. déficit en phosphatases alcalines --- r_associated #0: 20 --> en:leucinosis
    n1=déficit en phosphatases alcalines | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  50. déficit en pyruvate carboxylase --- r_associated #0: 20 --> en:leucinosis
    n1=déficit en pyruvate carboxylase | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  51. démence fronto-temporale --- r_associated #0: 20 --> en:leucinosis
    n1=démence fronto-temporale | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  52. en:(1) classic severe (onset of symptoms 4 to 7 days of age) --- r_associated #0: 20 --> en:leucinosis
    n1=en:(1) classic severe (onset of symptoms 4 to 7 days of age) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  53. en:(2) intermittent --- r_associated #0: 20 --> en:leucinosis
    n1=en:(2) intermittent | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  54. en:(3) intermediate --- r_associated #0: 20 --> en:leucinosis
    n1=en:(3) intermediate | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  55. en:(4) thiamine-responsive form --- r_associated #0: 20 --> en:leucinosis
    n1=en:(4) thiamine-responsive form | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  56. en:(5) dihydrolipoyl dehydrogenase (e3)-deficient --- r_associated #0: 20 --> en:leucinosis
    n1=en:(5) dihydrolipoyl dehydrogenase (e3)-deficient | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  57. en:17 alpha-hydroxyprogesterone aldolase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:17 alpha-hydroxyprogesterone aldolase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  58. en:17-beta-hydroxysteroid dehydrogenase 3 deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:17-beta-hydroxysteroid dehydrogenase 3 deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  59. en:17q21 microdeletion syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:17q21 microdeletion syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  60. en:1p36 deletion syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:1p36 deletion syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  61. en:2-hydroxyglutaric aciduria --- r_associated #0: 20 --> en:leucinosis
    n1=en:2-hydroxyglutaric aciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  62. en:21-hydroxylase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:21-hydroxylase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  63. en:22q telomere deletion syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:22q telomere deletion syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  64. en:3-methyl-2-oxobutanoate dehydrogenase (lipoamide) --- r_associated #0: 20 --> en:leucinosis
    n1=en:3-methyl-2-oxobutanoate dehydrogenase (lipoamide) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  65. en:3-methylglutaconic aciduria --- r_associated #0: 20 --> en:leucinosis
    n1=en:3-methylglutaconic aciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  66. en:3-methylglutaconic aciduria type 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:3-methylglutaconic aciduria type 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  67. en:3-methylglutaconic aciduria type 3 --- r_associated #0: 20 --> en:leucinosis
    n1=en:3-methylglutaconic aciduria type 3 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  68. en:3-methylglutaconic aciduria type 5 --- r_associated #0: 20 --> en:leucinosis
    n1=en:3-methylglutaconic aciduria type 5 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  69. en:3-methylglutaconic aciduria type iv --- r_associated #0: 20 --> en:leucinosis
    n1=en:3-methylglutaconic aciduria type iv | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  70. en:5 alpha steroid reductase 2 deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:5 alpha steroid reductase 2 deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  71. en:5' 10' methylenetetrahydrofolate reductase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:5' 10' methylenetetrahydrofolate reductase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  72. en:5-oxoprolinase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:5-oxoprolinase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  73. en:aagenaes syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:aagenaes syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  74. en:abetalipoproteinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:abetalipoproteinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  75. en:acatalasemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:acatalasemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  76. en:acetyl-coa: carboxylase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:acetyl-coa: carboxylase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  77. en:achard syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:achard syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  78. en:achenbach syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:achenbach syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  79. en:achondrogenesis --- r_associated #0: 20 --> en:leucinosis
    n1=en:achondrogenesis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  80. en:achondroplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:achondroplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  81. en:achromatopsia --- r_associated #0: 20 --> en:leucinosis
    n1=en:achromatopsia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  82. en:acid phosphatase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:acid phosphatase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  83. en:acquired hyperostosis syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:acquired hyperostosis syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  84. en:acquired lactase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:acquired lactase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  85. en:acrocallosal syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:acrocallosal syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  86. en:acrocephalosyndactyly --- r_associated #0: 20 --> en:leucinosis
    n1=en:acrocephalosyndactyly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  87. en:acrodermatitis --- r_associated #0: 20 --> en:leucinosis
    n1=en:acrodermatitis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  88. en:acrodermatitis enteropathica --- r_associated #0: 20 --> en:leucinosis
    n1=en:acrodermatitis enteropathica | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  89. en:acromegaly --- r_associated #0: 20 --> en:leucinosis
    n1=en:acromegaly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  90. en:acute intermittent porphyria --- r_associated #0: 20 --> en:leucinosis
    n1=en:acute intermittent porphyria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  91. en:acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:acyl-coa dehydrogenase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  92. en:acyl-coa dehydrogenase, short-chain deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:acyl-coa dehydrogenase, short-chain deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  93. en:adenine phosphoribosyltransferase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:adenine phosphoribosyltransferase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  94. en:adenylosuccinate lyase deficiency (disorder) --- r_associated #0: 20 --> en:leucinosis
    n1=en:adenylosuccinate lyase deficiency (disorder) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  95. en:adiposis dolorosa --- r_associated #0: 20 --> en:leucinosis
    n1=en:adiposis dolorosa | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  96. en:adrenal gland hyperplasia ii --- r_associated #0: 20 --> en:leucinosis
    n1=en:adrenal gland hyperplasia ii | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  97. en:adrenoleukodystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:adrenoleukodystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  98. en:adult hypophosphatasia (disorder) --- r_associated #0: 20 --> en:leucinosis
    n1=en:adult hypophosphatasia (disorder) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  99. en:afibrinogenemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:afibrinogenemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  100. en:agnosia --- r_associated #0: 20 --> en:leucinosis
    n1=en:agnosia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  101. en:aicardi syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:aicardi syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  102. en:ainhum --- r_associated #0: 20 --> en:leucinosis
    n1=en:ainhum | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  103. en:al awadi syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:al awadi syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  104. en:alagille syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:alagille syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  105. en:albinism --- r_associated #0: 20 --> en:leucinosis
    n1=en:albinism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  106. en:albinotic fundus --- r_associated #0: 20 --> en:leucinosis
    n1=en:albinotic fundus | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  107. en:albright's hereditary osteodystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:albright's hereditary osteodystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  108. en:aldosterone synthase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:aldosterone synthase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  109. en:alkaptonuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:alkaptonuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  110. en:allan-herndon-dudley syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:allan-herndon-dudley syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  111. en:allanson pantzar mcleod syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:allanson pantzar mcleod syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  112. en:allgrove syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:allgrove syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  113. en:alpha thalassemia x-linked mental retardation syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:alpha thalassemia x-linked mental retardation syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  114. en:alpha, alpha-trehalase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:alpha, alpha-trehalase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  115. en:alpha-1 antitrypsin deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:alpha-1 antitrypsin deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  116. en:alpha-fetoprotein deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:alpha-fetoprotein deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  117. en:alpha-methylacyl-coa racemase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:alpha-methylacyl-coa racemase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  118. en:alport syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:alport syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  119. en:alstrom syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:alstrom syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  120. en:amaurosis fugax --- r_associated #0: 20 --> en:leucinosis
    n1=en:amaurosis fugax | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  121. en:amelogenesis imperfecta - recessive - rough --- r_associated #0: 20 --> en:leucinosis
    n1=en:amelogenesis imperfecta - recessive - rough | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  122. en:amelogenesis imperfecta and gingival hyperplasia syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:amelogenesis imperfecta and gingival hyperplasia syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  123. en:amino acid deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:amino acid deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  124. en:amino acid metabolism disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:amino acid metabolism disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  125. en:amino acid transport disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:amino acid transport disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  126. en:amino acid transport disorders, inborn --- r_associated #0: 20 --> en:leucinosis
    n1=en:amino acid transport disorders, inborn | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  127. en:amino acid/carbohydrate metabolic disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:amino acid/carbohydrate metabolic disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  128. en:amino acidemia disorder suspected:prid:pt:bld.dot:nom --- r_associated #0: 20 --> en:leucinosis
    n1=en:amino acidemia disorder suspected:prid:pt:bld.dot:nom | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  129. en:amino acids, branched-chain --- r_associated #0: 20 --> en:leucinosis
    n1=en:amino acids, branched-chain | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  130. en:aminoaciduria --- r_associated #0: 20 --> en:leucinosis
    n1=en:aminoaciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  131. en:aminoacylase 1 deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:aminoacylase 1 deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  132. en:aminomethyltransferase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:aminomethyltransferase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  133. en:amniotic band syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:amniotic band syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  134. en:analbuminemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:analbuminemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  135. en:andersen syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:andersen syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  136. en:androgen insensitivity syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:androgen insensitivity syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  137. en:anemia, hypochromic microcytic, with iron overload --- r_associated #0: 20 --> en:leucinosis
    n1=en:anemia, hypochromic microcytic, with iron overload | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  138. en:anemia, sickle cell --- r_associated #0: 20 --> en:leucinosis
    n1=en:anemia, sickle cell | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  139. en:anencephaly --- r_associated #0: 20 --> en:leucinosis
    n1=en:anencephaly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  140. en:angelman syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:angelman syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  141. en:anhidrotic ectodermal dysplasia 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:anhidrotic ectodermal dysplasia 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  142. en:aniridia --- r_associated #0: 20 --> en:leucinosis
    n1=en:aniridia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  143. en:antithrombin iii deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:antithrombin iii deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  144. en:antley-bixler syndrome, autosomal dominant --- r_associated #0: 20 --> en:leucinosis
    n1=en:antley-bixler syndrome, autosomal dominant | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  145. en:aortic coarctation --- r_associated #0: 20 --> en:leucinosis
    n1=en:aortic coarctation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  146. en:aprosencephaly --- r_associated #0: 20 --> en:leucinosis
    n1=en:aprosencephaly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  147. en:arakawa syndrome ii --- r_associated #0: 20 --> en:leucinosis
    n1=en:arakawa syndrome ii | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  148. en:arginine:glycine amidinotransferase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:arginine:glycine amidinotransferase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  149. en:argininemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:argininemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  150. en:argininosuccinic aciduria --- r_associated #0: 20 --> en:leucinosis
    n1=en:argininosuccinic aciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  151. en:arnold-chiari malformation --- r_associated #0: 20 --> en:leucinosis
    n1=en:arnold-chiari malformation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  152. en:arrhythmogenic right ventricular dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:arrhythmogenic right ventricular dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  153. en:arterial tortuosity syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:arterial tortuosity syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  154. en:arthrogryposis --- r_associated #0: 20 --> en:leucinosis
    n1=en:arthrogryposis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  155. en:arthrogryposis multiplex congenita, neurogenic type (disorder) --- r_associated #0: 20 --> en:leucinosis
    n1=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  156. en:aspartylglycosaminuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:aspartylglycosaminuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  157. en:aspects of mortality statistics --- r_associated #0: 20 --> en:leucinosis
    n1=en:aspects of mortality statistics | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  158. en:aspects of radionuclide imaging --- r_associated #0: 20 --> en:leucinosis
    n1=en:aspects of radionuclide imaging | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  159. en:ataxia --- r_associated #0: 20 --> en:leucinosis
    n1=en:ataxia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  160. en:ataxia telangiectasia syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:ataxia telangiectasia syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  161. en:ataxia with vitamin e deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:ataxia with vitamin e deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  162. en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  163. en:ateliotic dwarfism without insulinopenia --- r_associated #0: 20 --> en:leucinosis
    n1=en:ateliotic dwarfism without insulinopenia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  164. en:atransferrinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:atransferrinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  165. en:atrophic muscular disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:atrophic muscular disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  166. en:atrophoderma vermiculatum --- r_associated #0: 20 --> en:leucinosis
    n1=en:atrophoderma vermiculatum | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  167. en:auditory perceptual disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:auditory perceptual disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  168. en:autoimmune lymphoproliferative syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:autoimmune lymphoproliferative syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  169. en:autoimmune polyendocrinopathy syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:autoimmune polyendocrinopathy syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  170. en:autoinflammation, lipodystrophy and dermatosis syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:autoinflammation, lipodystrophy and dermatosis syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  171. en:autosomal dominant disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal dominant disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  172. en:autosomal dominant optic atrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal dominant optic atrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  173. en:autosomal hereditary disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal hereditary disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  174. en:autosomal recessive asexual dwarfism --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal recessive asexual dwarfism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  175. en:autosomal recessive disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal recessive disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  176. en:autosomal recessive distal osteolysis syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal recessive distal osteolysis syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  177. en:autosomal recessive hypohidrotic ectodermal dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal recessive hypohidrotic ectodermal dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  178. en:autosomal recessive ichthyosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal recessive ichthyosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  179. en:autosomal recessive idiopathic familial dystonia --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal recessive idiopathic familial dystonia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  180. en:autosomal recessive inheritance --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal recessive inheritance | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  181. en:autosomal recessive muscular dystrophy with limb girdle distribution --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal recessive muscular dystrophy with limb girdle distribution | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  182. en:autosomal recessive ocular albinism --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal recessive ocular albinism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  183. en:autosomal recessive primary microcephaly --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal recessive primary microcephaly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  184. en:autosomal recessive scid --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal recessive scid | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  185. en:autosomal recessive sideroblastic anemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal recessive sideroblastic anemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  186. en:autosomal recessive spastic paraplegia type 11 --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal recessive spastic paraplegia type 11 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  187. en:autosomal recessive trait --- r_associated #0: 20 --> en:leucinosis
    n1=en:autosomal recessive trait | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  188. en:baller-gerold syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:baller-gerold syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  189. en:bannayan syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:bannayan syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  190. en:bardet-biedl syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:bardet-biedl syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  191. en:bartter syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:bartter syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  192. en:basal ganglia disease, biotin-responsive --- r_associated #0: 20 --> en:leucinosis
    n1=en:basal ganglia disease, biotin-responsive | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  193. en:bckdha gene --- r_associated #0: 20 --> en:leucinosis
    n1=en:bckdha gene | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  194. en:bckdhb gene --- r_associated #0: 20 --> en:leucinosis
    n1=en:bckdhb gene | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  195. en:beare-stevenson cutis gyrata syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:beare-stevenson cutis gyrata syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  196. en:becker generalized myotonia --- r_associated #0: 20 --> en:leucinosis
    n1=en:becker generalized myotonia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  197. en:beckwith-wiedemann syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:beckwith-wiedemann syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  198. en:behr syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:behr syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  199. en:behrens baumann dust syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:behrens baumann dust syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  200. en:benign mucous membrane pemphigoid --- r_associated #0: 20 --> en:leucinosis
    n1=en:benign mucous membrane pemphigoid | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  201. en:benign neonatal hyperaminoaciduria --- r_associated #0: 20 --> en:leucinosis
    n1=en:benign neonatal hyperaminoaciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  202. en:berardinelli-seip congenital lipodystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:berardinelli-seip congenital lipodystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  203. en:bernard-soulier syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:bernard-soulier syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  204. en:beta-aminoisobutyricaciduria --- r_associated #0: 20 --> en:leucinosis
    n1=en:beta-aminoisobutyricaciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  205. en:beta-ketothiolase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:beta-ketothiolase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  206. en:beta-methylcrotonylglycinuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:beta-methylcrotonylglycinuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  207. en:bietti crystalline corneoretinal dystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:bietti crystalline corneoretinal dystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  208. en:biotinidase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:biotinidase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  209. en:birt-hogg-dube syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:birt-hogg-dube syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  210. en:blepharophimosis syndrome ohdo type --- r_associated #0: 20 --> en:leucinosis
    n1=en:blepharophimosis syndrome ohdo type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  211. en:bloom syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:bloom syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  212. en:borderline mental retardation (i.q. 70-85) --- r_associated #0: 20 --> en:leucinosis
    n1=en:borderline mental retardation (i.q. 70-85) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  213. en:borjeson-forssman-lehmann syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:borjeson-forssman-lehmann syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  214. en:bothnia retinal dystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:bothnia retinal dystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  215. en:bowen-conradi syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:bowen-conradi syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  216. en:brachydactyly syndrome type b --- r_associated #0: 20 --> en:leucinosis
    n1=en:brachydactyly syndrome type b | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  217. en:brain diseases, metabolic, inborn --- r_associated #0: 20 --> en:leucinosis
    n1=en:brain diseases, metabolic, inborn | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  218. en:brain iron accumulation type i syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:brain iron accumulation type i syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  219. en:brain mri shows diffusion abnormalities --- r_associated #0: 20 --> en:leucinosis
    n1=en:brain mri shows diffusion abnormalities | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  220. en:branched chain ketoaciduria (alpha-keto isocaproate, alpha-keto-beta methylisovalerate, alpha-keto isovalerate) --- r_associated #0: 20 --> en:leucinosis
    n1=en:branched chain ketoaciduria (alpha-keto isocaproate, alpha-keto-beta methylisovalerate, alpha-keto isovalerate) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  221. en:brca1 mutation carrier --- r_associated #0: 20 --> en:leucinosis
    n1=en:brca1 mutation carrier | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  222. en:brca2 mutation carrier --- r_associated #0: 20 --> en:leucinosis
    n1=en:brca2 mutation carrier | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  223. en:brody myopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:brody myopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  224. en:brown-sequard syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:brown-sequard syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  225. en:brown-vialetto-van laere syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:brown-vialetto-van laere syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  226. en:butyryl-coa dehydrogenase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:butyryl-coa dehydrogenase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  227. en:cadasil syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:cadasil syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  228. en:calciphylaxis --- r_associated #0: 20 --> en:leucinosis
    n1=en:calciphylaxis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  229. en:campomelic dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:campomelic dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  230. en:camurati-engelmann syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:camurati-engelmann syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  231. en:cancer genetics --- r_associated #0: 20 --> en:leucinosis
    n1=en:cancer genetics | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  232. en:carbamoyl-phosphate synthetase i deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:carbamoyl-phosphate synthetase i deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  233. en:carbohydrate metabolism, inborn errors --- r_associated #0: 20 --> en:leucinosis
    n1=en:carbohydrate metabolism, inborn errors | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  234. en:carbohydrate-deficient glycoprotein syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:carbohydrate-deficient glycoprotein syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  235. en:cardio-facio-cutaneous syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:cardio-facio-cutaneous syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  236. en:cardiofaciocutaneous syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:cardiofaciocutaneous syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  237. en:carney complex --- r_associated #0: 20 --> en:leucinosis
    n1=en:carney complex | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  238. en:carnitine palmitoyltransferase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:carnitine palmitoyltransferase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  239. en:carnitine palmitoyltransferase i deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:carnitine palmitoyltransferase i deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  240. en:carnitine palmitoyltransferase ii deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:carnitine palmitoyltransferase ii deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  241. en:carnosinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:carnosinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  242. en:caroli disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:caroli disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  243. en:cartilage hair hypoplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:cartilage hair hypoplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  244. en:cask related intellectual disability --- r_associated #0: 20 --> en:leucinosis
    n1=en:cask related intellectual disability | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  245. en:cat-eye syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:cat-eye syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  246. en:cataplexy --- r_associated #0: 20 --> en:leucinosis
    n1=en:cataplexy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  247. en:caused by mutation in the branched chain keto acid dehydrogenase e1, alpha polypeptide gene (bckdha, 608348.0001) --- r_associated #0: 20 --> en:leucinosis
    n1=en:caused by mutation in the branched chain keto acid dehydrogenase e1, alpha polypeptide gene (bckdha, 608348.0001) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  248. en:caused by mutation in the branched chain keto acid dehydrogenase e1, beta polypeptide gene (bckdhb, 248611.0001) --- r_associated #0: 20 --> en:leucinosis
    n1=en:caused by mutation in the branched chain keto acid dehydrogenase e1, beta polypeptide gene (bckdhb, 248611.0001) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  249. en:caused by mutation in the dihydrolipoamide branched chain transacylase gene (dbt, 248610.0001) --- r_associated #0: 20 --> en:leucinosis
    n1=en:caused by mutation in the dihydrolipoamide branched chain transacylase gene (dbt, 248610.0001) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  250. en:caused by mutation in the dihydrolipoamide dehydrogenase gene (dld, 238331.0001) --- r_associated #0: 20 --> en:leucinosis
    n1=en:caused by mutation in the dihydrolipoamide dehydrogenase gene (dld, 238331.0001) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  251. en:cerebellar ataxia ectodermal dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:cerebellar ataxia ectodermal dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  252. en:cerebellar ataxia, cayman type --- r_associated #0: 20 --> en:leucinosis
    n1=en:cerebellar ataxia, cayman type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  253. en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  254. en:cerebral edema --- r_associated #0: 20 --> en:leucinosis
    n1=en:cerebral edema | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  255. en:cerebrooculofacioskeletal syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:cerebrooculofacioskeletal syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  256. en:cerebroretinal microangiopathy with calcifications and cysts (disorder) --- r_associated #0: 20 --> en:leucinosis
    n1=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  257. en:cerebrotendinous xanthomatosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:cerebrotendinous xanthomatosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  258. en:charcot-marie-tooth disease type 4 --- r_associated #0: 20 --> en:leucinosis
    n1=en:charcot-marie-tooth disease type 4 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  259. en:charge syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:charge syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  260. en:chemically induced --- r_associated #0: 20 --> en:leucinosis
    n1=en:chemically induced | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  261. en:chilblains --- r_associated #0: 20 --> en:leucinosis
    n1=en:chilblains | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  262. en:childhood hypophosphatasia (disorder) --- r_associated #0: 20 --> en:leucinosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  263. en:childhood myocerebrohepatopathy spectrum --- r_associated #0: 20 --> en:leucinosis
    n1=en:childhood myocerebrohepatopathy spectrum | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  264. en:chitty hall baraitser syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:chitty hall baraitser syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  265. en:chondrodysplasia punctata --- r_associated #0: 20 --> en:leucinosis
    n1=en:chondrodysplasia punctata | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  266. en:chondrodysplasia punctata syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:chondrodysplasia punctata syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  267. en:chorea --- r_associated #0: 20 --> en:leucinosis
    n1=en:chorea | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  268. en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism --- r_associated #0: 20 --> en:leucinosis
    n1=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  269. en:choroideremia --- r_associated #0: 20 --> en:leucinosis
    n1=en:choroideremia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  270. en:chromosome 2q37 deletion syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:chromosome 2q37 deletion syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  271. en:chromosome disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:chromosome disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  272. en:chylomicron retention disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:chylomicron retention disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  273. en:circulating enzyme deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:circulating enzyme deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  274. en:citrin deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:citrin deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  275. en:citrullinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:citrullinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  276. en:classical phenylketonuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:classical phenylketonuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  277. en:cleft lip/palate-ectodermal dysplasia syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:cleft lip/palate-ectodermal dysplasia syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  278. en:cleidocranial dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:cleidocranial dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  279. en:cockayne syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:cockayne syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  280. en:codas syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:codas syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  281. en:coffin-lowry syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:coffin-lowry syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  282. en:coffin-siris syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:coffin-siris syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  283. en:cogan-reese syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:cogan-reese syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  284. en:cohen syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:cohen syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  285. en:coma --- r_associated #0: 20 --> en:leucinosis
    n1=en:coma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  286. en:combined lipase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:combined lipase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  287. en:combined malonic and methylmalonic aciduria --- r_associated #0: 20 --> en:leucinosis
    n1=en:combined malonic and methylmalonic aciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  288. en:complete mevalonate kinase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:complete mevalonate kinase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  289. en:complex regional pain syndrome i --- r_associated #0: 20 --> en:leucinosis
    n1=en:complex regional pain syndrome i | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  290. en:complex regional pain syndrome ii --- r_associated #0: 20 --> en:leucinosis
    n1=en:complex regional pain syndrome ii | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  291. en:complication aspects --- r_associated #0: 20 --> en:leucinosis
    n1=en:complication aspects | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  292. en:conditions tested for in this newborn screening study:id:pt:bld.dot:nom --- r_associated #0: 20 --> en:leucinosis
    n1=en:conditions tested for in this newborn screening study:id:pt:bld.dot:nom | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  293. en:congenital --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  294. en:congenital adrenal hyperplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital adrenal hyperplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  295. en:congenital alpha-2-antiplasmin deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital alpha-2-antiplasmin deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  296. en:congenital amegakaryocytic thrombocytopenia --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital amegakaryocytic thrombocytopenia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  297. en:congenital bilateral aplasia of the vas deferens --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital bilateral aplasia of the vas deferens | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  298. en:congenital bowing of long bone --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital bowing of long bone | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  299. en:congenital cataracts, facial dysmorphism, and neuropathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital cataracts, facial dysmorphism, and neuropathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  300. en:congenital combined immunodeficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital combined immunodeficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  301. en:congenital cortical hyperostosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital cortical hyperostosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  302. en:congenital disorder of deglycosylation --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital disorder of deglycosylation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  303. en:congenital disorder of glycosylation type ia --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital disorder of glycosylation type ia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  304. en:congenital disorder of glycosylation type ic --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital disorder of glycosylation type ic | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  305. en:congenital disorder of glycosylation type ig --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital disorder of glycosylation type ig | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  306. en:congenital disorder of natural immunity --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital disorder of natural immunity | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  307. en:congenital dyserythropoietic anemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital dyserythropoietic anemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  308. en:congenital dyserythropoietic anemia, type i --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital dyserythropoietic anemia, type i | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  309. en:congenital dyserythropoietic anemia, type ii --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital dyserythropoietic anemia, type ii | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  310. en:congenital fiber-type disproportion --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital fiber-type disproportion | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  311. en:congenital ichthyosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital ichthyosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  312. en:congenital insensitivity to pain with anhidrosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital insensitivity to pain with anhidrosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  313. en:congenital leptin deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital leptin deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  314. en:congenital leucocyte abnormality --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital leucocyte abnormality | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  315. en:congenital metabolic disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital metabolic disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  316. en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  317. en:congenital myasthenic syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital myasthenic syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  318. en:congenital neutropenia --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital neutropenia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  319. en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  320. en:congenital pain insensitivity --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital pain insensitivity | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  321. en:congenital pancreatic enterokinase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital pancreatic enterokinase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  322. en:congenital plasminogen activator inhibitor deficiency type 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital plasminogen activator inhibitor deficiency type 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  323. en:congenital pure red cell aplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital pure red cell aplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  324. en:congenital structural myopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital structural myopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  325. en:congenital sucrase-isomaltase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital sucrase-isomaltase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  326. en:congenital t-cell immunodeficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital t-cell immunodeficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  327. en:congenital transferrin deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:congenital transferrin deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  328. en:connexin 26 gene anomaly --- r_associated #0: 20 --> en:leucinosis
    n1=en:connexin 26 gene anomaly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  329. en:cor triatriatum --- r_associated #0: 20 --> en:leucinosis
    n1=en:cor triatriatum | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  330. en:corpus callosum agenesis neuronopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:corpus callosum agenesis neuronopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  331. en:costello syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:costello syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  332. en:cowden syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:cowden syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  333. en:craniodiaphyseal dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:craniodiaphyseal dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  334. en:cranioectodermal dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:cranioectodermal dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  335. en:craniofacial dysostosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:craniofacial dysostosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  336. en:craniosynostosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:craniosynostosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  337. en:crigler-najjar syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:crigler-najjar syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  338. en:crisponi syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:crisponi syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  339. en:cryopyrin-associated periodic syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:cryopyrin-associated periodic syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  340. en:cryptophthalmos syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:cryptophthalmos syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  341. en:cutis laxa --- r_associated #0: 20 --> en:leucinosis
    n1=en:cutis laxa | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  342. en:cutis laxa, autosomal recessive --- r_associated #0: 20 --> en:leucinosis
    n1=en:cutis laxa, autosomal recessive | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  343. en:cystathionine beta-synthase deficiency disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:cystathionine beta-synthase deficiency disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  344. en:cystathioninuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:cystathioninuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  345. en:cystic fibrosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:cystic fibrosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  346. en:cystinosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:cystinosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  347. en:cystinuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:cystinuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  348. en:cytochrome-c oxidase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:cytochrome-c oxidase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  349. en:d-bifunctional protein deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:d-bifunctional protein deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  350. en:d-glyceric aciduria --- r_associated #0: 20 --> en:leucinosis
    n1=en:d-glyceric aciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  351. en:dandy-walker malformation --- r_associated #0: 20 --> en:leucinosis
    n1=en:dandy-walker malformation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  352. en:darier disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:darier disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  353. en:de barsy syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:de barsy syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  354. en:de sanctis-cacchione syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:de sanctis-cacchione syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  355. en:deafness, autosomal recessive 1a --- r_associated #0: 20 --> en:leucinosis
    n1=en:deafness, autosomal recessive 1a | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  356. en:deafness, autosomal recessive 28 --- r_associated #0: 20 --> en:leucinosis
    n1=en:deafness, autosomal recessive 28 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  357. en:deafness, autosomal recessive 49 --- r_associated #0: 20 --> en:leucinosis
    n1=en:deafness, autosomal recessive 49 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  358. en:deafness, congenital, with inner ear agenesis, microtia, and microdontia --- r_associated #0: 20 --> en:leucinosis
    n1=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  359. en:deafness, progressive, with stapes fixation --- r_associated #0: 20 --> en:leucinosis
    n1=en:deafness, progressive, with stapes fixation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  360. en:deafness, sensorineural, and male infertility --- r_associated #0: 20 --> en:leucinosis
    n1=en:deafness, sensorineural, and male infertility | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  361. en:death in untreated children --- r_associated #0: 20 --> en:leucinosis
    n1=en:death in untreated children | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  362. en:defect in post-translational modification of lysosomal enzymes --- r_associated #0: 20 --> en:leucinosis
    n1=en:defect in post-translational modification of lysosomal enzymes | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  363. en:deficiency in enzyme complexes of mitochondrial respiratory chain --- r_associated #0: 20 --> en:leucinosis
    n1=en:deficiency in enzyme complexes of mitochondrial respiratory chain | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  364. en:deficiency of fructokinase --- r_associated #0: 20 --> en:leucinosis
    n1=en:deficiency of fructokinase | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  365. en:deficiency of glucosyltransferase 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:deficiency of glucosyltransferase 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  366. en:deficiency of steryl-sulfatase --- r_associated #0: 20 --> en:leucinosis
    n1=en:deficiency of steryl-sulfatase | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  367. en:deletion 18p syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:deletion 18p syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  368. en:deletion 18q syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:deletion 18q syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  369. en:dent disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:dent disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  370. en:dentatorubral-pallidoluysian atrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:dentatorubral-pallidoluysian atrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  371. en:dentinogenesis imperfecta --- r_associated #0: 20 --> en:leucinosis
    n1=en:dentinogenesis imperfecta | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  372. en:desmosterolosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:desmosterolosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  373. en:developmental hereditary disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:developmental hereditary disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  374. en:dextrocardia --- r_associated #0: 20 --> en:leucinosis
    n1=en:dextrocardia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  375. en:diagnosis aspect --- r_associated #0: 20 --> en:leucinosis
    n1=en:diagnosis aspect | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  376. en:dicarboxylicaminoaciduria --- r_associated #0: 20 --> en:leucinosis
    n1=en:dicarboxylicaminoaciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  377. en:diffuse cerebral sclerosis of schilder --- r_associated #0: 20 --> en:leucinosis
    n1=en:diffuse cerebral sclerosis of schilder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  378. en:diffuse idiopathic skeletal hyperostosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:diffuse idiopathic skeletal hyperostosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  379. en:dihydropyrimidinase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:dihydropyrimidinase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  380. en:dihydropyrimidine dehydrogenase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:dihydropyrimidine dehydrogenase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  381. en:dihydrouracil dehydrogenase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:dihydrouracil dehydrogenase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  382. en:disorder due to cytochrome p450 enzyme variant --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder due to cytochrome p450 enzyme variant | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  383. en:disorder due to n-acetyltransferase enzyme variant --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder due to n-acetyltransferase enzyme variant | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  384. en:disorder of amino acid and organic acid metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder of amino acid and organic acid metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  385. en:disorder of aromatic amino acid metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder of aromatic amino acid metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  386. en:disorder of branched-chain amino acid metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder of branched-chain amino acid metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  387. en:disorder of carnitine metabolism, unspecified --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder of carnitine metabolism, unspecified | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  388. en:disorder of creatine synthesis --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder of creatine synthesis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  389. en:disorder of glycoprotein metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder of glycoprotein metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  390. en:disorder of glycosaminoglycan metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder of glycosaminoglycan metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  391. en:disorder of histidine metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder of histidine metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  392. en:disorder of lysine and hydroxylysine metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder of lysine and hydroxylysine metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  393. en:disorder of pyruvate metabolism and mitochondrial respiratory chain --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder of pyruvate metabolism and mitochondrial respiratory chain | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  394. en:disorder of sialic acid metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder of sialic acid metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  395. en:disorder of sulfur-bearing amino acid metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder of sulfur-bearing amino acid metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  396. en:disorder of valine metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorder of valine metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  397. en:disorders of branched-chain amino-acid metabolism and fatty-acid metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:disorders of branched-chain amino-acid metabolism and fatty-acid metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  398. en:dna repair disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:dna repair disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  399. en:donnai-barrow syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:donnai-barrow syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  400. en:donohue syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:donohue syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  401. en:down syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:down syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  402. en:drug- and toxin-induced pulmonary arterial hypertension --- r_associated #0: 20 --> en:leucinosis
    n1=en:drug- and toxin-induced pulmonary arterial hypertension | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  403. en:duane syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:duane syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  404. en:dubin-johnson syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:dubin-johnson syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  405. en:dubowitz syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:dubowitz syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  406. en:dyggve-melchior-clausen syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:dyggve-melchior-clausen syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  407. en:dyschromatosis symmetrica hereditaria --- r_associated #0: 20 --> en:leucinosis
    n1=en:dyschromatosis symmetrica hereditaria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  408. en:dyskeratosis congenita --- r_associated #0: 20 --> en:leucinosis
    n1=en:dyskeratosis congenita | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  409. en:dyskeratosis congenita, autosomal recessive --- r_associated #0: 20 --> en:leucinosis
    n1=en:dyskeratosis congenita, autosomal recessive | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  410. en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  411. en:ear, patella, short stature syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:ear, patella, short stature syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  412. en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  413. en:ebstein anomaly --- r_associated #0: 20 --> en:leucinosis
    n1=en:ebstein anomaly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  414. en:ectodermal dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:ectodermal dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  415. en:ectodermal dysplasia/ skin fragility syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:ectodermal dysplasia/ skin fragility syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  416. en:ectrodactyly --- r_associated #0: 20 --> en:leucinosis
    n1=en:ectrodactyly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  417. en:ectromelia --- r_associated #0: 20 --> en:leucinosis
    n1=en:ectromelia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  418. en:ehlers-danlos syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:ehlers-danlos syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  419. en:ehlers-danlos syndrome, arthrochalasia type --- r_associated #0: 20 --> en:leucinosis
    n1=en:ehlers-danlos syndrome, arthrochalasia type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  420. en:ehlers-danlos syndrome, type vi --- r_associated #0: 20 --> en:leucinosis
    n1=en:ehlers-danlos syndrome, type vi | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  421. en:elevated plasma alloisoleucine --- r_associated #0: 20 --> en:leucinosis
    n1=en:elevated plasma alloisoleucine | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  422. en:elevated plasma branched chain amino acids (leucine, isoleucine, valine) --- r_associated #0: 20 --> en:leucinosis
    n1=en:elevated plasma branched chain amino acids (leucine, isoleucine, valine) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  423. en:ellis-van creveld syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:ellis-van creveld syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  424. en:embryologic --- r_associated #0: 20 --> en:leucinosis
    n1=en:embryologic | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  425. en:empty sella syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:empty sella syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  426. en:encephalocele --- r_associated #0: 20 --> en:leucinosis
    n1=en:encephalocele | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  427. en:encephalopathy due to sulfite oxidase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:encephalopathy due to sulfite oxidase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  428. en:enterokinase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:enterokinase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  429. en:enzymology --- r_associated #0: 20 --> en:leucinosis
    n1=en:enzymology | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  430. en:epidemiologic --- r_associated #0: 20 --> en:leucinosis
    n1=en:epidemiologic | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  431. en:epidermolysis bullosa --- r_associated #0: 20 --> en:leucinosis
    n1=en:epidermolysis bullosa | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  432. en:epidermolysis bullosa simplex with pyloric atresia --- r_associated #0: 20 --> en:leucinosis
    n1=en:epidermolysis bullosa simplex with pyloric atresia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  433. en:epiphyseal dysplasia, multiple, 4 --- r_associated #0: 20 --> en:leucinosis
    n1=en:epiphyseal dysplasia, multiple, 4 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  434. en:episodic pain syndrome, familial, 3 --- r_associated #0: 20 --> en:leucinosis
    n1=en:episodic pain syndrome, familial, 3 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  435. en:erythrokeratodermia variabilis --- r_associated #0: 20 --> en:leucinosis
    n1=en:erythrokeratodermia variabilis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  436. en:erythromelalgia --- r_associated #0: 20 --> en:leucinosis
    n1=en:erythromelalgia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  437. en:erythropoietic porphyria --- r_associated #0: 20 --> en:leucinosis
    n1=en:erythropoietic porphyria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  438. en:erythropoietic protoporphyria --- r_associated #0: 20 --> en:leucinosis
    n1=en:erythropoietic protoporphyria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  439. en:ethanolaminosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:ethanolaminosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  440. en:ethnologic --- r_associated #0: 20 --> en:leucinosis
    n1=en:ethnologic | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  441. en:etiology aspects --- r_associated #0: 20 --> en:leucinosis
    n1=en:etiology aspects | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  442. en:exfoliation syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:exfoliation syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  443. en:exposure as collected domain --- r_associated #0: 20 --> en:leucinosis
    n1=en:exposure as collected domain | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  444. en:factor v and factor viii, combined deficiency of --- r_associated #0: 20 --> en:leucinosis
    n1=en:factor v and factor viii, combined deficiency of | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  445. en:factor v leiden --- r_associated #0: 20 --> en:leucinosis
    n1=en:factor v leiden | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  446. en:familial acantholysis --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial acantholysis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  447. en:familial acute myeloid leukemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial acute myeloid leukemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  448. en:familial adenomatous polyposis --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial adenomatous polyposis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  449. en:familial amyloidosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial amyloidosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  450. en:familial c3b inhibitor deficiency syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial c3b inhibitor deficiency syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  451. en:familial carcinoid syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial carcinoid syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  452. en:familial chordoma --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial chordoma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  453. en:familial chronic lymphocytic leukemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial chronic lymphocytic leukemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  454. en:familial dysautonomia --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial dysautonomia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  455. en:familial erythrocytosis due to diphosphoglycerate mutase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  456. en:familial hemorrhagic diathesis --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial hemorrhagic diathesis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  457. en:familial hodgkin lymphoma --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial hodgkin lymphoma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  458. en:familial hypercalciuric hypocalcemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial hypercalciuric hypocalcemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  459. en:familial hypertrophic cardiomyopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial hypertrophic cardiomyopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  460. en:familial hypoaldosteronism --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial hypoaldosteronism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  461. en:familial hypocalciuric hypercalcemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial hypocalciuric hypercalcemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  462. en:familial hypothyroidism --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial hypothyroidism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  463. en:familial isolated hyperparathyroidism --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial isolated hyperparathyroidism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  464. en:familial juvenile nephronophthisis --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial juvenile nephronophthisis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  465. en:familial mediterranean fever --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial mediterranean fever | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  466. en:familial multiple myeloma --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial multiple myeloma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  467. en:familial neuroblastoma --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial neuroblastoma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  468. en:familial non-medullary thyroid cancer --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial non-medullary thyroid cancer | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  469. en:familial partial lipodystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial partial lipodystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  470. en:familial periodic paralysis --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial periodic paralysis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  471. en:familial primary hypomagnesemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial primary hypomagnesemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  472. en:familial renal iminoglycinuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial renal iminoglycinuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  473. en:familial testicular germ cell tumor --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial testicular germ cell tumor | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  474. en:familial waldenstrom macroglobulinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:familial waldenstrom macroglobulinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  475. en:fanconi anemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:fanconi anemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  476. en:fanconi syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:fanconi syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  477. en:farber lipogranulomatosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:farber lipogranulomatosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  478. en:fatal familial insomnia --- r_associated #0: 20 --> en:leucinosis
    n1=en:fatal familial insomnia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  479. en:fatal infantile lactic acidosis with methylmalonic aciduria --- r_associated #0: 20 --> en:leucinosis
    n1=en:fatal infantile lactic acidosis with methylmalonic aciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  480. en:fatty acid hydroxylase-associated neurodegeneration --- r_associated #0: 20 --> en:leucinosis
    n1=en:fatty acid hydroxylase-associated neurodegeneration | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  481. en:fatty acid metabolism disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:fatty acid metabolism disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  482. en:feeding problem --- r_associated #0: 20 --> en:leucinosis
    n1=en:feeding problem | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  483. en:feingold syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:feingold syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  484. en:felty syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:felty syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  485. en:female restricted epilepsy with intellectual disability syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:female restricted epilepsy with intellectual disability syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  486. en:ferrochelatase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:ferrochelatase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  487. en:fetal akinesia deformation sequence --- r_associated #0: 20 --> en:leucinosis
    n1=en:fetal akinesia deformation sequence | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  488. en:fetus with hereditary disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:fetus with hereditary disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  489. en:fibrodysplasia ossificans progressiva --- r_associated #0: 20 --> en:leucinosis
    n1=en:fibrodysplasia ossificans progressiva | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  490. en:fibromuscular dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:fibromuscular dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  491. en:fibular hypoplasia and complex brachydactyly --- r_associated #0: 20 --> en:leucinosis
    n1=en:fibular hypoplasia and complex brachydactyly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  492. en:five clinical variants of msud unassociated with genotype --- r_associated #0: 20 --> en:leucinosis
    n1=en:five clinical variants of msud unassociated with genotype | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  493. en:focal dermal hypoplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:focal dermal hypoplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  494. en:folinic acid responsive seizure syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:folinic acid responsive seizure syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  495. en:fox-fordyce disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:fox-fordyce disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  496. en:fragile x syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:fragile x syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  497. en:fraser syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:fraser syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  498. en:fraxe intellectual disability syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:fraxe intellectual disability syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  499. en:friedreich ataxia --- r_associated #0: 20 --> en:leucinosis
    n1=en:friedreich ataxia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  500. en:fronto-facio-nasal dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:fronto-facio-nasal dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  501. en:frontonasal dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:frontonasal dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  502. en:frontotemporal dementia --- r_associated #0: 20 --> en:leucinosis
    n1=en:frontotemporal dementia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  503. en:fructose-1,6-bisphosphatase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:fructose-1,6-bisphosphatase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  504. en:fryns macrocephaly --- r_associated #0: 20 --> en:leucinosis
    n1=en:fryns macrocephaly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  505. en:fryns syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:fryns syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  506. en:fuchs endothelial dystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:fuchs endothelial dystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  507. en:fucosidosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:fucosidosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  508. en:galactosemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:galactosemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  509. en:gamma-glutamyltransferase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:gamma-glutamyltransferase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  510. en:gangrenous stomatitis --- r_associated #0: 20 --> en:leucinosis
    n1=en:gangrenous stomatitis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  511. en:gastric antral vascular ectasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:gastric antral vascular ectasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  512. en:gastroschisis --- r_associated #0: 20 --> en:leucinosis
    n1=en:gastroschisis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  513. en:gaucher disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:gaucher disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  514. en:gaze palsy, familial horizontal, with progressive scoliosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:gaze palsy, familial horizontal, with progressive scoliosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  515. en:generalized arterial calcification of infancy 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:generalized arterial calcification of infancy 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  516. en:generalized myotonia of thomsen --- r_associated #0: 20 --> en:leucinosis
    n1=en:generalized myotonia of thomsen | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  517. en:genetic aspects --- r_associated #0: 20 --> en:leucinosis
    n1=en:genetic aspects | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  518. en:genetic brain disorders --- r_associated #0: 20 --> en:leucinosis
    n1=en:genetic brain disorders | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  519. en:genetic syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:genetic syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  520. en:genu varum --- r_associated #0: 20 --> en:leucinosis
    n1=en:genu varum | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  521. en:geroderma osteodysplastica --- r_associated #0: 20 --> en:leucinosis
    n1=en:geroderma osteodysplastica | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  522. en:gerstmann-straussler-scheinker disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:gerstmann-straussler-scheinker disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  523. en:giacci familial neurogenic acroosteolysis --- r_associated #0: 20 --> en:leucinosis
    n1=en:giacci familial neurogenic acroosteolysis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  524. en:giant axonal neuropathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:giant axonal neuropathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  525. en:gitelman syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:gitelman syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  526. en:glanzmann thrombasthenia --- r_associated #0: 20 --> en:leucinosis
    n1=en:glanzmann thrombasthenia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  527. en:glucose-6-phosphate dehydrogenase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:glucose-6-phosphate dehydrogenase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  528. en:glucose-6-phosphate dehydrogenase deficiency anemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:glucose-6-phosphate dehydrogenase deficiency anemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  529. en:glutamate formiminotransferase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:glutamate formiminotransferase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  530. en:glutamate-cysteine ligase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:glutamate-cysteine ligase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  531. en:glutaric acidemia type 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:glutaric acidemia type 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  532. en:glutathione s-transferase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:glutathione s-transferase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  533. en:glutathione synthetase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:glutathione synthetase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  534. en:glycine dehydrogenase (decarboxylating) deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:glycine dehydrogenase (decarboxylating) deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  535. en:glycine encephalopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:glycine encephalopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  536. en:glycogen storage disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:glycogen storage disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  537. en:glycogen storage disease type i --- r_associated #0: 20 --> en:leucinosis
    n1=en:glycogen storage disease type i | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  538. en:glycogen storage disease type x --- r_associated #0: 20 --> en:leucinosis
    n1=en:glycogen storage disease type x | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  539. en:goldenhar syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:goldenhar syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  540. en:goniodysgenesis-mental retardation-short stature syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  541. en:goodpasture syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:goodpasture syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  542. en:gracile syndrome (disorder) --- r_associated #0: 20 --> en:leucinosis
    n1=en:gracile syndrome (disorder) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  543. en:granular corneal dystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:granular corneal dystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  544. en:gray platelet syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:gray platelet syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  545. en:griscelli syndrome type 2 --- r_associated #0: 20 --> en:leucinosis
    n1=en:griscelli syndrome type 2 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  546. en:gurrieri sammito bellussi syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:gurrieri sammito bellussi syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  547. en:gynatresia --- r_associated #0: 20 --> en:leucinosis
    n1=en:gynatresia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  548. en:gyrate atrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:gyrate atrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  549. en:hajdu-cheney syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:hajdu-cheney syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  550. en:hallermann syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:hallermann syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  551. en:hallucination --- r_associated #0: 20 --> en:leucinosis
    n1=en:hallucination | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  552. en:hantavirus pulmonary syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:hantavirus pulmonary syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  553. en:hard skin syndrome parana type --- r_associated #0: 20 --> en:leucinosis
    n1=en:hard skin syndrome parana type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  554. en:harrod doman keele syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:harrod doman keele syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  555. en:hartnup disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:hartnup disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  556. en:hellp syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:hellp syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  557. en:hemochromatosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:hemochromatosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  558. en:hemoglobinopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:hemoglobinopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  559. en:hemolytic anemia due to pyruvate kinase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:hemolytic anemia due to pyruvate kinase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  560. en:hemophagocytic lymphohistiocytosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:hemophagocytic lymphohistiocytosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  561. en:hemophilia a --- r_associated #0: 20 --> en:leucinosis
    n1=en:hemophilia a | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  562. en:hemophilia b --- r_associated #0: 20 --> en:leucinosis
    n1=en:hemophilia b | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  563. en:hemorrhagic fever with renal syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:hemorrhagic fever with renal syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  564. en:hepatolenticular degeneration --- r_associated #0: 20 --> en:leucinosis
    n1=en:hepatolenticular degeneration | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  565. en:hereditary adrenal unresponsiveness to corticotropin --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary adrenal unresponsiveness to corticotropin | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  566. en:hereditary angioedema --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary angioedema | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  567. en:hereditary breast and ovarian cancer syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary breast and ovarian cancer syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  568. en:hereditary breast/ovarian cancer - brca1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary breast/ovarian cancer - brca1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  569. en:hereditary breast/ovarian cancer - brca2 --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary breast/ovarian cancer - brca2 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  570. en:hereditary central nervous system demyelinating diseases --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary central nervous system demyelinating diseases | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  571. en:hereditary cerebral amyloid angiopathy, icelandic type --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary cerebral amyloid angiopathy, icelandic type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  572. en:hereditary coagulation factor deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary coagulation factor deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  573. en:hereditary connective tissue disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary connective tissue disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  574. en:hereditary coproporphyria --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary coproporphyria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  575. en:hereditary diffuse gastric adenocarcinoma --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary diffuse gastric adenocarcinoma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  576. en:hereditary disease in family possibly affecting fetus --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary disease in family possibly affecting fetus | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  577. en:hereditary disease in family possibly affecting fetus, affecting management of mother --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary disease in family possibly affecting fetus, affecting management of mother | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  578. en:hereditary disease in family possibly affecting fetus, affecting management of mother, antepartum condition or complication --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary disease in family possibly affecting fetus, affecting management of mother, antepartum condition or complication | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  579. en:hereditary disease in family possibly affecting fetus, affecting management of mother, unspecified as to episode of care in pregnancy --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary disease in family possibly affecting fetus, affecting management of mother, unspecified as to episode of care in pregnancy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  580. en:hereditary disease in family possibly affecting fetus, affecting management of mother, with delivery --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary disease in family possibly affecting fetus, affecting management of mother, with delivery | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  581. en:hereditary disorder by system --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary disorder by system | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  582. en:hereditary dysplasminogenemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary dysplasminogenemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  583. en:hereditary elliptocytosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary elliptocytosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  584. en:hereditary factor x deficiency disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary factor x deficiency disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  585. en:hereditary factor xi deficiency disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary factor xi deficiency disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  586. en:hereditary factor xii deficiency disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary factor xii deficiency disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  587. en:hereditary fructose intolerance --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary fructose intolerance | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  588. en:hereditary gastrointestinal stromal tumor --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary gastrointestinal stromal tumor | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  589. en:hereditary hemorrhagic telangiectasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary hemorrhagic telangiectasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  590. en:hereditary hyperbilirubinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary hyperbilirubinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  591. en:hereditary hypoplasminogenemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary hypoplasminogenemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  592. en:hereditary kidney oncocytoma --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary kidney oncocytoma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  593. en:hereditary leiomyomatosis and renal cell cancer --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary leiomyomatosis and renal cell cancer | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  594. en:hereditary melanoma --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary melanoma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  595. en:hereditary methemoglobinemia, enzymatic type --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary methemoglobinemia, enzymatic type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  596. en:hereditary motor end-plate disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary motor end-plate disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  597. en:hereditary mucosal leukokeratosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary mucosal leukokeratosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  598. en:hereditary multiple exostoses --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary multiple exostoses | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  599. en:hereditary neoplastic syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary neoplastic syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  600. en:hereditary orotic aciduria --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary orotic aciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  601. en:hereditary palmoplantar keratoderma gamborg nielsen type --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary palmoplantar keratoderma gamborg nielsen type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  602. en:hereditary pancreatic carcinoma --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary pancreatic carcinoma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  603. en:hereditary pancreatitis --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary pancreatitis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  604. en:hereditary papillary renal cell carcinoma --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary papillary renal cell carcinoma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  605. en:hereditary paraganglioma --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary paraganglioma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  606. en:hereditary peripheral nervous system disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary peripheral nervous system disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  607. en:hereditary persistence of fetal hemoglobin --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary persistence of fetal hemoglobin | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  608. en:hereditary renal cell cancer --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary renal cell cancer | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  609. en:hereditary retinoblastoma --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary retinoblastoma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  610. en:hereditary spastic paralysis, infantile onset ascending --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary spastic paralysis, infantile onset ascending | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  611. en:hereditary spherocytosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary spherocytosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  612. en:hereditary thyroglossal duct cysts --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary thyroglossal duct cysts | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  613. en:hereditary thyroid gland medullary carcinoma --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary thyroid gland medullary carcinoma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  614. en:hereditary wilms tumor --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary wilms tumor | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  615. en:hereditary xanthinuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:hereditary xanthinuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  616. en:heritable pulmonary arterial hypertension --- r_associated #0: 20 --> en:leucinosis
    n1=en:heritable pulmonary arterial hypertension | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  617. en:hermansky-pudlak syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:hermansky-pudlak syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  618. en:heterotaxy syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:heterotaxy syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  619. en:high molecular weight kininogen deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:high molecular weight kininogen deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  620. en:histidinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:histidinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  621. en:historical aspects qualifier --- r_associated #0: 20 --> en:leucinosis
    n1=en:historical aspects qualifier | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  622. en:hmg-coa lyase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:hmg-coa lyase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  623. en:hnsha due to aldolase a deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:hnsha due to aldolase a deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  624. en:hnsha due to diphosphoglycerate mutase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  625. en:hnsha due to glucose phosphate isomerase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:hnsha due to glucose phosphate isomerase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  626. en:hnsha due to glutathione reductase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:hnsha due to glutathione reductase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  627. en:hnsha due to glutathione synthetase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:hnsha due to glutathione synthetase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  628. en:hnsha due to hexokinase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:hnsha due to hexokinase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  629. en:hnsha due to nadh diaphorase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:hnsha due to nadh diaphorase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  630. en:hnsha due to pyrimidine-5'-nucleotidase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  631. en:holmes-adie syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:holmes-adie syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  632. en:holocarboxylase synthetase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:holocarboxylase synthetase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  633. en:holoprosencephaly --- r_associated #0: 20 --> en:leucinosis
    n1=en:holoprosencephaly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  634. en:holt-oram syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:holt-oram syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  635. en:homocarnosinosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:homocarnosinosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  636. en:homocystinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:homocystinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  637. en:homocystinuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:homocystinuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  638. en:huntington's disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:huntington's disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  639. en:hyaline membrane syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyaline membrane syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  640. en:hydroa vacciniforme --- r_associated #0: 20 --> en:leucinosis
    n1=en:hydroa vacciniforme | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  641. en:hydrops fetalis --- r_associated #0: 20 --> en:leucinosis
    n1=en:hydrops fetalis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  642. en:hydroxykynureninuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:hydroxykynureninuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  643. en:hydroxyprolinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hydroxyprolinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  644. en:hymenolepiasis --- r_associated #0: 20 --> en:leucinosis
    n1=en:hymenolepiasis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  645. en:hyperandrogenism due to non-classic 21-hydroxylase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperandrogenism due to non-classic 21-hydroxylase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  646. en:hyperglycerolemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperglycerolemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  647. en:hyperglycinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperglycinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  648. en:hyperhomocysteinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperhomocysteinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  649. en:hyperimmunoglobulin e syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperimmunoglobulin e syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  650. en:hyperimmunoglobulin syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperimmunoglobulin syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  651. en:hyperkalemic periodic paralysis --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperkalemic periodic paralysis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  652. en:hyperleucine-isoleucinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperleucine-isoleucinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  653. en:hyperleucinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperleucinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  654. en:hyperlipoproteinemia type i --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperlipoproteinemia type i | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  655. en:hyperlysinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperlysinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  656. en:hypermanganesemia with dystonia polycythemia and cirrhosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:hypermanganesemia with dystonia polycythemia and cirrhosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  657. en:hypermethioniuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:hypermethioniuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  658. en:hyperornithinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperornithinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  659. en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  660. en:hyperphenylalaninemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperphenylalaninemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  661. en:hyperphenylalaninemia, non phenylketonuric --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperphenylalaninemia, non phenylketonuric | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  662. en:hyperphosphatasia with mental retardation --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperphosphatasia with mental retardation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  663. en:hyperpipecolatemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperpipecolatemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  664. en:hyperprolinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperprolinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  665. en:hyperprolinemia type 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperprolinemia type 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  666. en:hyperprolinemia type 2 --- r_associated #0: 20 --> en:leucinosis
    n1=en:hyperprolinemia type 2 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  667. en:hypertonia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hypertonia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  668. en:hypoalphalipoproteinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hypoalphalipoproteinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  669. en:hypoglycemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hypoglycemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  670. en:hypohidrotic ectodermal dysplasia with immune deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:hypohidrotic ectodermal dysplasia with immune deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  671. en:hypokalemia, familial --- r_associated #0: 20 --> en:leucinosis
    n1=en:hypokalemia, familial | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  672. en:hypokalemic periodic paralysis --- r_associated #0: 20 --> en:leucinosis
    n1=en:hypokalemic periodic paralysis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  673. en:hypomagnesemia 1, intestinal --- r_associated #0: 20 --> en:leucinosis
    n1=en:hypomagnesemia 1, intestinal | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  674. en:hypomyelination and congenital cataract --- r_associated #0: 20 --> en:leucinosis
    n1=en:hypomyelination and congenital cataract | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  675. en:hypophosphatasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hypophosphatasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  676. en:hypophosphatemic rickets with hypercalciuria, hereditary --- r_associated #0: 20 --> en:leucinosis
    n1=en:hypophosphatemic rickets with hypercalciuria, hereditary | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  677. en:hypospadias-mental retardation syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:hypospadias-mental retardation syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  678. en:hypotonia --- r_associated #0: 20 --> en:leucinosis
    n1=en:hypotonia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  679. en:i-cell disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:i-cell disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  680. en:ichthyosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:ichthyosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  681. en:idiopathic cd4-positive t-lymphocytopenia --- r_associated #0: 20 --> en:leucinosis
    n1=en:idiopathic cd4-positive t-lymphocytopenia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  682. en:idiopathic hypersomnolence --- r_associated #0: 20 --> en:leucinosis
    n1=en:idiopathic hypersomnolence | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  683. en:immunodeficiency with hyper-igm type 2 --- r_associated #0: 20 --> en:leucinosis
    n1=en:immunodeficiency with hyper-igm type 2 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  684. en:immunoglobulin a deficiency 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:immunoglobulin a deficiency 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  685. en:immunology aspects --- r_associated #0: 20 --> en:leucinosis
    n1=en:immunology aspects | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  686. en:imperforate anus --- r_associated #0: 20 --> en:leucinosis
    n1=en:imperforate anus | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  687. en:imperforate vagina --- r_associated #0: 20 --> en:leucinosis
    n1=en:imperforate vagina | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  688. en:in blood --- r_associated #0: 20 --> en:leucinosis
    n1=en:in blood | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  689. en:in cerebrospinal fluid --- r_associated #0: 20 --> en:leucinosis
    n1=en:in cerebrospinal fluid | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  690. en:in inbred old order mennonite population of lancaster county, msud prevalence is 1/176 newborns --- r_associated #0: 20 --> en:leucinosis
    n1=en:in inbred old order mennonite population of lancaster county, msud prevalence is 1/176 newborns | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  691. en:in urine --- r_associated #0: 20 --> en:leucinosis
    n1=en:in urine | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  692. en:inborn biological transport disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:inborn biological transport disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  693. en:inborn error of glutathione metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:inborn error of glutathione metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  694. en:inborn error of lipoprotein metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:inborn error of lipoprotein metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  695. en:inborn errors of bilirubin metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:inborn errors of bilirubin metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  696. en:inborn errors of carbohydrate metabolism (excl glucose) --- r_associated #0: 20 --> en:leucinosis
    n1=en:inborn errors of carbohydrate metabolism (excl glucose) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  697. en:inborn errors of porphyrin metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:inborn errors of porphyrin metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  698. en:inborn errors of steroid synthesis --- r_associated #0: 20 --> en:leucinosis
    n1=en:inborn errors of steroid synthesis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  699. en:inborn immunodeficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:inborn immunodeficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  700. en:inborn lipid/lipoprotein disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:inborn lipid/lipoprotein disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  701. en:incontinentia pigmenti --- r_associated #0: 20 --> en:leucinosis
    n1=en:incontinentia pigmenti | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  702. en:increased aromatase activity --- r_associated #0: 20 --> en:leucinosis
    n1=en:increased aromatase activity | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  703. en:infantile globoid cell leukodystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:infantile globoid cell leukodystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  704. en:infantile hypophosphatasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:infantile hypophosphatasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  705. en:infantile neuroaxonal dystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:infantile neuroaxonal dystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  706. en:infantile refsum disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:infantile refsum disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  707. en:inflammatory hereditary disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:inflammatory hereditary disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  708. en:inherited aminoaciduria --- r_associated #0: 20 --> en:leucinosis
    n1=en:inherited aminoaciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  709. en:inherited disorder of bilirubin metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:inherited disorder of bilirubin metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  710. en:inherited disorder of folate metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:inherited disorder of folate metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  711. en:inherited disorder of thyroid metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:inherited disorder of thyroid metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  712. en:inherited factor ii deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:inherited factor ii deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  713. en:inherited metabolic disorder of nervous system --- r_associated #0: 20 --> en:leucinosis
    n1=en:inherited metabolic disorder of nervous system | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  714. en:inherited predisposition to essential thrombocythemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:inherited predisposition to essential thrombocythemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  715. en:insulin growth factor i resistance --- r_associated #0: 20 --> en:leucinosis
    n1=en:insulin growth factor i resistance | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  716. en:interleukin-1 receptor-associated kinase 4 deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:interleukin-1 receptor-associated kinase 4 deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  717. en:intermediary metabolism disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:intermediary metabolism disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  718. en:intermediate maple syrup urine disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:intermediate maple syrup urine disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  719. en:intermittent branched-chain ketonuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:intermittent branched-chain ketonuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  720. en:intermittent maple syrup urine disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:intermittent maple syrup urine disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  721. en:intestinal atresia --- r_associated #0: 20 --> en:leucinosis
    n1=en:intestinal atresia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  722. en:intestinal disaccharidase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:intestinal disaccharidase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  723. en:intestinal epithelial dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:intestinal epithelial dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  724. en:iridocorneal endothelial syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:iridocorneal endothelial syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  725. en:isaacs syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:isaacs syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  726. en:isolated hyperchlorhidrosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:isolated hyperchlorhidrosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  727. en:isolated hypoplasia of the right ventricle --- r_associated #0: 20 --> en:leucinosis
    n1=en:isolated hypoplasia of the right ventricle | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  728. en:isoleucine --- r_associated #0: 20 --> en:leucinosis
    n1=en:isoleucine | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  729. en:isovaleric acidemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:isovaleric acidemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  730. en:jackson-weiss syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:jackson-weiss syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  731. en:jacobsen syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:jacobsen syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  732. en:jankovic rivera syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:jankovic rivera syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  733. en:jervell and lange nielsen syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:jervell and lange nielsen syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  734. en:jeune syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:jeune syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  735. en:joubert syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:joubert syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  736. en:juvenile polyposis syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:juvenile polyposis syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  737. en:juvenile x-linked retinoschisis --- r_associated #0: 20 --> en:leucinosis
    n1=en:juvenile x-linked retinoschisis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  738. en:kabuki syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:kabuki syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  739. en:kallmann syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:kallmann syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  740. en:karandikar maria kamble syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:karandikar maria kamble syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  741. en:kartagener syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:kartagener syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  742. en:kaufman-mckusick syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:kaufman-mckusick syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  743. en:kearns-sayre syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:kearns-sayre syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  744. en:kernicterus --- r_associated #0: 20 --> en:leucinosis
    n1=en:kernicterus | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  745. en:ketonemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:ketonemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  746. en:ketonuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:ketonuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  747. en:ketosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:ketosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  748. en:kimura disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:kimura disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  749. en:kleine-levin syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:kleine-levin syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  750. en:klinefelter syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:klinefelter syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  751. en:klippel-feil syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:klippel-feil syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  752. en:klippel-trenaunay-weber syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:klippel-trenaunay-weber syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  753. en:kluver-bucy syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:kluver-bucy syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  754. en:kniest dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:kniest dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  755. en:knobloch syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:knobloch syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  756. en:kohlschutter tonz syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:kohlschutter tonz syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  757. en:korsakoff syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:korsakoff syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  758. en:kshv inflammatory cytokine syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:kshv inflammatory cytokine syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  759. en:kuskokwim disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:kuskokwim disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  760. en:lactase deficiency, congenital --- r_associated #0: 20 --> en:leucinosis
    n1=en:lactase deficiency, congenital | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  761. en:lactic acidosis in e3-deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:lactic acidosis in e3-deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  762. en:lactose intolerance, adult type --- r_associated #0: 20 --> en:leucinosis
    n1=en:lactose intolerance, adult type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  763. en:lafora disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:lafora disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  764. en:landau-kleffner syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:landau-kleffner syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  765. en:laron syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:laron syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  766. en:lateral medullary syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:lateral medullary syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  767. en:laurence-moon syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:laurence-moon syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  768. en:leber congenital amaurosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:leber congenital amaurosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  769. en:leber hereditary optic atrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:leber hereditary optic atrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  770. en:lecithin acyltransferase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:lecithin acyltransferase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  771. en:leigh disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:leigh disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  772. en:lennox-gastaut syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:lennox-gastaut syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  773. en:leopard syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:leopard syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  774. en:leprosy --- r_associated #0: 20 --> en:leucinosis
    n1=en:leprosy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  775. en:leptospirosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:leptospirosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  776. en:leri-weill dyschondrosteosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:leri-weill dyschondrosteosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  777. en:lesch-nyhan syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:lesch-nyhan syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  778. en:lethal congenital contracture syndrome 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:lethal congenital contracture syndrome 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  779. en:lethal congenital contracture syndrome 2 --- r_associated #0: 20 --> en:leucinosis
    n1=en:lethal congenital contracture syndrome 2 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  780. en:lethal congenital contracture syndrome type 3 --- r_associated #0: 20 --> en:leucinosis
    n1=en:lethal congenital contracture syndrome type 3 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  781. en:lethargy --- r_associated #0: 20 --> en:leucinosis
    n1=en:lethargy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  782. en:leukodystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:leukodystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  783. en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation --- r_associated #0: 20 --> en:leucinosis
    n1=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  784. en:leukotriene c4 synthase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:leukotriene c4 synthase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  785. en:levocardia --- r_associated #0: 20 --> en:leucinosis
    n1=en:levocardia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  786. en:li-fraumeni syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:li-fraumeni syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  787. en:liddle syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:liddle syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  788. en:life-threatening metabolic decompensation --- r_associated #0: 20 --> en:leucinosis
    n1=en:life-threatening metabolic decompensation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  789. en:lig4 syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:lig4 syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  790. en:lipid metabolism disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:lipid metabolism disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  791. en:lipid metabolism, inborn errors --- r_associated #0: 20 --> en:leucinosis
    n1=en:lipid metabolism, inborn errors | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  792. en:lipoid congenital adrenal hyperplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:lipoid congenital adrenal hyperplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  793. en:lipoid proteinosis of urbach and wiethe --- r_associated #0: 20 --> en:leucinosis
    n1=en:lipoid proteinosis of urbach and wiethe | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  794. en:lipoprotein glomerulopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:lipoprotein glomerulopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  795. en:lissencephaly --- r_associated #0: 20 --> en:leucinosis
    n1=en:lissencephaly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  796. en:lissencephaly syndrome, norman-roberts type --- r_associated #0: 20 --> en:leucinosis
    n1=en:lissencephaly syndrome, norman-roberts type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  797. en:loeys-dietz syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:loeys-dietz syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  798. en:long-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:long-chain acyl-coa dehydrogenase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  799. en:lubs x-linked mental retardation syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:lubs x-linked mental retardation syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  800. en:lujan fryns syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:lujan fryns syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  801. en:lynch syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:lynch syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  802. en:lysinuric protein intolerance --- r_associated #0: 20 --> en:leucinosis
    n1=en:lysinuric protein intolerance | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  803. en:lysosomal storage disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:lysosomal storage disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  804. en:lysosomal storage diseases, nervous system --- r_associated #0: 20 --> en:leucinosis
    n1=en:lysosomal storage diseases, nervous system | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  805. en:macdermot winter syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:macdermot winter syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  806. en:machado-joseph disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:machado-joseph disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  807. en:macular corneal dystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:macular corneal dystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  808. en:majeed syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:majeed syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  809. en:malakoplakia --- r_associated #0: 20 --> en:leucinosis
    n1=en:malakoplakia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  810. en:malformations of cortical development --- r_associated #0: 20 --> en:leucinosis
    n1=en:malformations of cortical development | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  811. en:malignant atrophic papulosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:malignant atrophic papulosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  812. en:malignant hyperthermia syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:malignant hyperthermia syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  813. en:mallory-weiss syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:mallory-weiss syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  814. en:mandibuloacral dysplasia with type a lipodystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:mandibuloacral dysplasia with type a lipodystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  815. en:mannosidosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:mannosidosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  816. en:mansonelliasis --- r_associated #0: 20 --> en:leucinosis
    n1=en:mansonelliasis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  817. en:maple syrup urine disease, e3 deficient, with lactic acidosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:maple syrup urine disease, e3 deficient, with lactic acidosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  818. en:maple syrup urine disease, type 1a --- r_associated #0: 20 --> en:leucinosis
    n1=en:maple syrup urine disease, type 1a | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  819. en:maple syrup urine disease, type 1b --- r_associated #0: 20 --> en:leucinosis
    n1=en:maple syrup urine disease, type 1b | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  820. en:maple syrup urine disease, type ii --- r_associated #0: 20 --> en:leucinosis
    n1=en:maple syrup urine disease, type ii | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  821. en:maple syrup urine disease:imp:pt:bld.dot:nom --- r_associated #0: 20 --> en:leucinosis
    n1=en:maple syrup urine disease:imp:pt:bld.dot:nom | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  822. en:marburg virus disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:marburg virus disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  823. en:marfan syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:marfan syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  824. en:marfanoid mental retardation syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:marfanoid mental retardation syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  825. en:marles greenberg persaud syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:marles greenberg persaud syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  826. en:maroteaux-lamy syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:maroteaux-lamy syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  827. en:marshall syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:marshall syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  828. en:masa syndrome (disorder) --- r_associated #0: 20 --> en:leucinosis
    n1=en:masa syndrome (disorder) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  829. en:mayer-rokitansky-kuster-hauser syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:mayer-rokitansky-kuster-hauser syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  830. en:mcdonough syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:mcdonough syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  831. en:meckel-gruber syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:meckel-gruber syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  832. en:medium-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:medium-chain acyl-coa dehydrogenase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  833. en:meesmann corneal dystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:meesmann corneal dystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  834. en:megalencephalic leukoencephalopathy with subcortical cysts --- r_associated #0: 20 --> en:leucinosis
    n1=en:megalencephalic leukoencephalopathy with subcortical cysts | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  835. en:mehes syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:mehes syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  836. en:melas syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:melas syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  837. en:melkersson-rosenthal syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:melkersson-rosenthal syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  838. en:melorheostosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:melorheostosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  839. en:mendelian disorders --- r_associated #0: 20 --> en:leucinosis
    n1=en:mendelian disorders | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  840. en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  841. en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  842. en:meningeal tuberculosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:meningeal tuberculosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  843. en:menkes disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:menkes disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  844. en:mental retardation --- r_associated #0: 20 --> en:leucinosis
    n1=en:mental retardation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  845. en:mental retardation if untreated --- r_associated #0: 20 --> en:leucinosis
    n1=en:mental retardation if untreated | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  846. en:mental retardation, x-linked, snyder-robinson type --- r_associated #0: 20 --> en:leucinosis
    n1=en:mental retardation, x-linked, snyder-robinson type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  847. en:merrf syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:merrf syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  848. en:metabolic aspects --- r_associated #0: 20 --> en:leucinosis
    n1=en:metabolic aspects | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  849. en:metabolic disorder being monitored:prid:pt:bld.dot:nom --- r_associated #0: 20 --> en:leucinosis
    n1=en:metabolic disorder being monitored:prid:pt:bld.dot:nom | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  850. en:metacarpal 4-5 fusion --- r_associated #0: 20 --> en:leucinosis
    n1=en:metacarpal 4-5 fusion | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  851. en:metal metabolism, inborn errors --- r_associated #0: 20 --> en:leucinosis
    n1=en:metal metabolism, inborn errors | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  852. en:methionine adenosyltransferase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:methionine adenosyltransferase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  853. en:methylcrotonyl-coa carboxylase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:methylcrotonyl-coa carboxylase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  854. en:methylene thf reductase deficiency and homocystinuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:methylene thf reductase deficiency and homocystinuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  855. en:methylenetetrahydrofolate reductase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:methylenetetrahydrofolate reductase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  856. en:methylenetetrahydrofolate reductase gene mutation --- r_associated #0: 20 --> en:leucinosis
    n1=en:methylenetetrahydrofolate reductase gene mutation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  857. en:methylmalonic acidemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:methylmalonic acidemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  858. en:methylmalonic aciduria --- r_associated #0: 20 --> en:leucinosis
    n1=en:methylmalonic aciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  859. en:methylmalonyl-coenzyme a mutase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:methylmalonyl-coenzyme a mutase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  860. en:mevalonate kinase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:mevalonate kinase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  861. en:microbiological --- r_associated #0: 20 --> en:leucinosis
    n1=en:microbiological | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  862. en:microcephalic primordial dwarfism toriello type --- r_associated #0: 20 --> en:leucinosis
    n1=en:microcephalic primordial dwarfism toriello type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  863. en:microcephaly and chorioretinopathy, autosomal recessive, type 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  864. en:microcephaly cervical spine fusion anomalies --- r_associated #0: 20 --> en:leucinosis
    n1=en:microcephaly cervical spine fusion anomalies | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  865. en:microcephaly deafness syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:microcephaly deafness syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  866. en:microcephaly, amish type (disorder) --- r_associated #0: 20 --> en:leucinosis
    n1=en:microcephaly, amish type (disorder) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  867. en:microcephaly-capillary malformation syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  868. en:microphthalmia, syndromic 4 (disorder) --- r_associated #0: 20 --> en:leucinosis
    n1=en:microphthalmia, syndromic 4 (disorder) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  869. en:migrating partial seizures in infancy --- r_associated #0: 20 --> en:leucinosis
    n1=en:migrating partial seizures in infancy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  870. en:mild mental retardation --- r_associated #0: 20 --> en:leucinosis
    n1=en:mild mental retardation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  871. en:miller-mckusick-malvaux-syndrome (3m syndrome) --- r_associated #0: 20 --> en:leucinosis
    n1=en:miller-mckusick-malvaux-syndrome (3m syndrome) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  872. en:mitochondrial dna depletion syndrome 2 (myopathic type) --- r_associated #0: 20 --> en:leucinosis
    n1=en:mitochondrial dna depletion syndrome 2 (myopathic type) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  873. en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  874. en:mitochondrial neurogastrointestingal encephalopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:mitochondrial neurogastrointestingal encephalopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  875. en:mitochondrial trifunctional protein deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:mitochondrial trifunctional protein deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  876. en:mixed connective tissue disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:mixed connective tissue disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  877. en:mmih syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:mmih syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  878. en:mobius syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:mobius syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  879. en:moderate mental retardation (i.q. 35-49) --- r_associated #0: 20 --> en:leucinosis
    n1=en:moderate mental retardation (i.q. 35-49) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  880. en:moderate steroid 21-hydroxylase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:moderate steroid 21-hydroxylase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  881. en:molybdenum cofactor deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:molybdenum cofactor deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  882. en:monilethrix --- r_associated #0: 20 --> en:leucinosis
    n1=en:monilethrix | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  883. en:morm syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:morm syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  884. en:morquio syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:morquio syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  885. en:mosaic variegated aneuploidy --- r_associated #0: 20 --> en:leucinosis
    n1=en:mosaic variegated aneuploidy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  886. en:mowat-wilson syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:mowat-wilson syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  887. en:moyamoya disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:moyamoya disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  888. en:mucopolysaccharidosis type i --- r_associated #0: 20 --> en:leucinosis
    n1=en:mucopolysaccharidosis type i | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  889. en:muenke syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:muenke syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  890. en:mulibrey nanism --- r_associated #0: 20 --> en:leucinosis
    n1=en:mulibrey nanism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  891. en:mullerian inhibiting factor deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:mullerian inhibiting factor deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  892. en:multicentric osteolysis nodulosis arthropathy spectrum --- r_associated #0: 20 --> en:leucinosis
    n1=en:multicentric osteolysis nodulosis arthropathy spectrum | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  893. en:multicentric osteolysis, nodulosis, and arthropathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:multicentric osteolysis, nodulosis, and arthropathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  894. en:multiple acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:multiple acyl-coa dehydrogenase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  895. en:multiple carboxylase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:multiple carboxylase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  896. en:multiple endocrine neoplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:multiple endocrine neoplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  897. en:multiple endocrine neoplasia type 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:multiple endocrine neoplasia type 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  898. en:multiple endocrine neoplasia type 2a --- r_associated #0: 20 --> en:leucinosis
    n1=en:multiple endocrine neoplasia type 2a | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  899. en:multiple osteochondromas --- r_associated #0: 20 --> en:leucinosis
    n1=en:multiple osteochondromas | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  900. en:multiple sulfatase deficiency disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:multiple sulfatase deficiency disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  901. en:multiple system atrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:multiple system atrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  902. en:muscle amp deaminase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:muscle amp deaminase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  903. en:muscle d-lactate dehydrogenase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:muscle d-lactate dehydrogenase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  904. en:muscle l-lactate dehydrogenase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:muscle l-lactate dehydrogenase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  905. en:muscle-eye-brain disease, congenital muscular dystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:muscle-eye-brain disease, congenital muscular dystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  906. en:muscular dystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:muscular dystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  907. en:mutagenic disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:mutagenic disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  908. en:mutyh-associated polyposis --- r_associated #0: 20 --> en:leucinosis
    n1=en:mutyh-associated polyposis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  909. en:myelocerebellar disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:myelocerebellar disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  910. en:myhre syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:myhre syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  911. en:myoglobinuria, recurrent --- r_associated #0: 20 --> en:leucinosis
    n1=en:myoglobinuria, recurrent | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  912. en:myokymia --- r_associated #0: 20 --> en:leucinosis
    n1=en:myokymia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  913. en:myopathy with exercise intolerance, swedish type --- r_associated #0: 20 --> en:leucinosis
    n1=en:myopathy with exercise intolerance, swedish type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  914. en:myopathy, early-onset, with fatal cardiomyopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:myopathy, early-onset, with fatal cardiomyopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  915. en:myositis --- r_associated #0: 20 --> en:leucinosis
    n1=en:myositis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  916. en:myotonic disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:myotonic disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  917. en:n-acetylglutamate synthase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:n-acetylglutamate synthase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  918. en:n-methylsuccinimide --- r_associated #0: 20 --> en:leucinosis
    n1=en:n-methylsuccinimide | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  919. en:nadh cytochrome b5 reductase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:nadh cytochrome b5 reductase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  920. en:nadh dehydrogenase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:nadh dehydrogenase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  921. en:nail-patella syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:nail-patella syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  922. en:nathalie syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:nathalie syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  923. en:naxos disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:naxos disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  924. en:nelson syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:nelson syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  925. en:neonatal progeroid syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:neonatal progeroid syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  926. en:neonatal research network terminology --- r_associated #0: 20 --> en:leucinosis
    n1=en:neonatal research network terminology | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  927. en:nephrocalcinosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:nephrocalcinosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  928. en:nephrogenic fibrosing dermopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:nephrogenic fibrosing dermopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  929. en:netherton syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:netherton syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  930. en:neural tube defect --- r_associated #0: 20 --> en:leucinosis
    n1=en:neural tube defect | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  931. en:neuraminidase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:neuraminidase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  932. en:neuroacanthocytosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:neuroacanthocytosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  933. en:neurocysticercosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:neurocysticercosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  934. en:neurodegeneration due to cerebral folate transport deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:neurodegeneration due to cerebral folate transport deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  935. en:neurodegeneration with brain iron accumulation 4 --- r_associated #0: 20 --> en:leucinosis
    n1=en:neurodegeneration with brain iron accumulation 4 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  936. en:neurofibromatosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:neurofibromatosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  937. en:neurofibromatosis type 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:neurofibromatosis type 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  938. en:neurofibromatosis type 2 --- r_associated #0: 20 --> en:leucinosis
    n1=en:neurofibromatosis type 2 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  939. en:neuromyelitis optica --- r_associated #0: 20 --> en:leucinosis
    n1=en:neuromyelitis optica | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  940. en:neuronal ceroid lipofuscinosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:neuronal ceroid lipofuscinosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  941. en:neuronal intranuclear inclusion disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:neuronal intranuclear inclusion disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  942. en:neuropathy, hereditary sensory and autonomic, type vii --- r_associated #0: 20 --> en:leucinosis
    n1=en:neuropathy, hereditary sensory and autonomic, type vii | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  943. en:neurotoxicity syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:neurotoxicity syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  944. en:neutral lipid storage disease with myopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:neutral lipid storage disease with myopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  945. en:nevoid basal cell carcinoma syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:nevoid basal cell carcinoma syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  946. en:newborn conditions with equivocal markers:prid:pt:bld.dot:nom --- r_associated #0: 20 --> en:leucinosis
    n1=en:newborn conditions with equivocal markers:prid:pt:bld.dot:nom | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  947. en:newborn conditions with positive markers:prid:pt:bld.dot:nom --- r_associated #0: 20 --> en:leucinosis
    n1=en:newborn conditions with positive markers:prid:pt:bld.dot:nom | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  948. en:niemann-pick disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:niemann-pick disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  949. en:nijmegen breakage syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:nijmegen breakage syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  950. en:non-hodgkin lymphoma --- r_associated #0: 20 --> en:leucinosis
    n1=en:non-hodgkin lymphoma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  951. en:non-trisomic autosomal aneuploidy --- r_associated #0: 20 --> en:leucinosis
    n1=en:non-trisomic autosomal aneuploidy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  952. en:nonaka myopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:nonaka myopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  953. en:norrie syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:norrie syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  954. en:north american indian childhood cirrhosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:north american indian childhood cirrhosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  955. en:northern epilepsy syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:northern epilepsy syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  956. en:nursing therapy --- r_associated #0: 20 --> en:leucinosis
    n1=en:nursing therapy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  957. en:nutritional management --- r_associated #0: 20 --> en:leucinosis
    n1=en:nutritional management | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  958. en:nutritional mental retardation --- r_associated #0: 20 --> en:leucinosis
    n1=en:nutritional mental retardation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  959. en:obesity due to melanocortin 4 receptor deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:obesity due to melanocortin 4 receptor deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  960. en:ochronosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:ochronosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  961. en:oculocerebral hypopigmentation syndrome type preus --- r_associated #0: 20 --> en:leucinosis
    n1=en:oculocerebral hypopigmentation syndrome type preus | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  962. en:oculocerebrorenal syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:oculocerebrorenal syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  963. en:oculocutaneous albinism type 4 --- r_associated #0: 20 --> en:leucinosis
    n1=en:oculocutaneous albinism type 4 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  964. en:oculootoradial syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:oculootoradial syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  965. en:odontohypophosphatasia (disorder) --- r_associated #0: 20 --> en:leucinosis
    n1=en:odontohypophosphatasia (disorder) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  966. en:oeis complex --- r_associated #0: 20 --> en:leucinosis
    n1=en:oeis complex | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  967. en:olivopontocerebellar atrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:olivopontocerebellar atrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  968. en:opitz trigonocephaly syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:opitz trigonocephaly syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  969. en:optic neuritis --- r_associated #0: 20 --> en:leucinosis
    n1=en:optic neuritis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  970. en:organic acid metabolism disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:organic acid metabolism disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  971. en:ornithine carbamoyltransferase deficiency disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  972. en:orofacial cleft 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:orofacial cleft 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  973. en:orofaciodigital syndrome type 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:orofaciodigital syndrome type 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  974. en:orofaciodigital syndrome type 6 --- r_associated #0: 20 --> en:leucinosis
    n1=en:orofaciodigital syndrome type 6 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  975. en:orotic aciduria --- r_associated #0: 20 --> en:leucinosis
    n1=en:orotic aciduria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  976. en:ossification of posterior longitudinal ligament --- r_associated #0: 20 --> en:leucinosis
    n1=en:ossification of posterior longitudinal ligament | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  977. en:osteochondrodysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:osteochondrodysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  978. en:osteogenesis imperfecta --- r_associated #0: 20 --> en:leucinosis
    n1=en:osteogenesis imperfecta | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  979. en:osteopetrosis with renal tubular acidosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:osteopetrosis with renal tubular acidosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  980. en:osteopoikilosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:osteopoikilosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  981. en:other disorders of aromatic amino-acid metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:other disorders of aromatic amino-acid metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  982. en:other disorders of branched-chain amino-acid metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:other disorders of branched-chain amino-acid metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  983. en:other disturbances of straight-chain amino-acid metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:other disturbances of straight-chain amino-acid metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  984. en:other mental retardation --- r_associated #0: 20 --> en:leucinosis
    n1=en:other mental retardation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  985. en:other specified disorders of amino-acid metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:other specified disorders of amino-acid metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  986. en:other specified disorders of amino-acid transport and metabolism --- r_associated #0: 20 --> en:leucinosis
    n1=en:other specified disorders of amino-acid transport and metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  987. en:otoonychoperoneal syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:otoonychoperoneal syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  988. en:otopalatodigital syndrome type 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:otopalatodigital syndrome type 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  989. en:pachyonychia congenita --- r_associated #0: 20 --> en:leucinosis
    n1=en:pachyonychia congenita | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  990. en:pain agnosia --- r_associated #0: 20 --> en:leucinosis
    n1=en:pain agnosia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  991. en:pallister-hall syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:pallister-hall syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  992. en:pallister-killian syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:pallister-killian syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  993. en:pancreatic alpha-amylase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:pancreatic alpha-amylase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  994. en:pancreatic colipase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:pancreatic colipase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  995. en:pancreatic lipase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:pancreatic lipase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  996. en:pancreatic triacylglycerol lipase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:pancreatic triacylglycerol lipase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  997. en:pancreatic trypsinogen deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:pancreatic trypsinogen deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  998. en:pancreatitis --- r_associated #0: 20 --> en:leucinosis
    n1=en:pancreatitis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  999. en:pantothenate kinase-associated neurodegeneration --- r_associated #0: 20 --> en:leucinosis
    n1=en:pantothenate kinase-associated neurodegeneration | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1000. en:panuveitis --- r_associated #0: 20 --> en:leucinosis
    n1=en:panuveitis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1001. en:papillon-lefevre syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:papillon-lefevre syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1002. en:paragonimiasis --- r_associated #0: 20 --> en:leucinosis
    n1=en:paragonimiasis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1003. en:parasitology --- r_associated #0: 20 --> en:leucinosis
    n1=en:parasitology | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1004. en:paroxysmal extreme pain disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:paroxysmal extreme pain disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1005. en:partington x-linked mental retardation syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:partington x-linked mental retardation syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1006. en:pathological aspects --- r_associated #0: 20 --> en:leucinosis
    n1=en:pathological aspects | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1007. en:pearson marrow-pancreas syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:pearson marrow-pancreas syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1008. en:pediatric terminology --- r_associated #0: 20 --> en:leucinosis
    n1=en:pediatric terminology | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1009. en:peeling skin syndrome, acral type --- r_associated #0: 20 --> en:leucinosis
    n1=en:peeling skin syndrome, acral type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1010. en:pelger-huet anomaly --- r_associated #0: 20 --> en:leucinosis
    n1=en:pelger-huet anomaly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1011. en:pelizaeus merzbacher like disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:pelizaeus merzbacher like disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1012. en:pelizaeus-merzbacher disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:pelizaeus-merzbacher disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1013. en:pemphigoid gestationis --- r_associated #0: 20 --> en:leucinosis
    n1=en:pemphigoid gestationis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1014. en:pentalogy of cantrell --- r_associated #0: 20 --> en:leucinosis
    n1=en:pentalogy of cantrell | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1015. en:pentosuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:pentosuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1016. en:peritoneal panniculitis --- r_associated #0: 20 --> en:leucinosis
    n1=en:peritoneal panniculitis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1017. en:perniola krajewska carnevale syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:perniola krajewska carnevale syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1018. en:peroxisomal disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:peroxisomal disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1019. en:persistent fetal circulation --- r_associated #0: 20 --> en:leucinosis
    n1=en:persistent fetal circulation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1020. en:persistent mullerian duct syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:persistent mullerian duct syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1021. en:perthes disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:perthes disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1022. en:peters-plus syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:peters-plus syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1023. en:pettigrew syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:pettigrew syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1024. en:pharmacotherapeutic --- r_associated #0: 20 --> en:leucinosis
    n1=en:pharmacotherapeutic | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1025. en:phenylketonuria --- r_associated #0: 20 --> en:leucinosis
    n1=en:phenylketonuria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1026. en:phenylketonuria ii --- r_associated #0: 20 --> en:leucinosis
    n1=en:phenylketonuria ii | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1027. en:phosphoenolpyruvate carboxykinase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:phosphoenolpyruvate carboxykinase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1028. en:phosphoglycerate kinase 1 deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:phosphoglycerate kinase 1 deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1029. en:physiopathological --- r_associated #0: 20 --> en:leucinosis
    n1=en:physiopathological | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1030. en:pick's disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:pick's disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1031. en:piebaldism --- r_associated #0: 20 --> en:leucinosis
    n1=en:piebaldism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1032. en:pierre robin syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:pierre robin syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1033. en:pinta --- r_associated #0: 20 --> en:leucinosis
    n1=en:pinta | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1034. en:piriformis muscle syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:piriformis muscle syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1035. en:pityriasis lichenoides --- r_associated #0: 20 --> en:leucinosis
    n1=en:pityriasis lichenoides | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1036. en:pityriasis rubra pilaris --- r_associated #0: 20 --> en:leucinosis
    n1=en:pityriasis rubra pilaris | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1037. en:placental steroid sulfatase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:placental steroid sulfatase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1038. en:plague --- r_associated #0: 20 --> en:leucinosis
    n1=en:plague | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1039. en:plummer-vinson syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:plummer-vinson syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1040. en:poland syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:poland syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1041. en:polycystic kidney disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:polycystic kidney disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1042. en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1043. en:polygenic hereditary disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:polygenic hereditary disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1044. en:pontocerebellar hypoplasia type 2 --- r_associated #0: 20 --> en:leucinosis
    n1=en:pontocerebellar hypoplasia type 2 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1045. en:popliteal pterygium syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:popliteal pterygium syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1046. en:porokeratosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:porokeratosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1047. en:porphobilinogen synthase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:porphobilinogen synthase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1048. en:porphyria cutanea tarda --- r_associated #0: 20 --> en:leucinosis
    n1=en:porphyria cutanea tarda | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1049. en:positive urine dnph screening test --- r_associated #0: 20 --> en:leucinosis
    n1=en:positive urine dnph screening test | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1050. en:postaxial polydactyly type a --- r_associated #0: 20 --> en:leucinosis
    n1=en:postaxial polydactyly type a | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1051. en:postaxial polydactyly, type b --- r_associated #0: 20 --> en:leucinosis
    n1=en:postaxial polydactyly, type b | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1052. en:potocki-lupski syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:potocki-lupski syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1053. en:potocki-shaffer syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:potocki-shaffer syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1054. en:prader-willi habitus, osteopenia, and camptodactyly --- r_associated #0: 20 --> en:leucinosis
    n1=en:prader-willi habitus, osteopenia, and camptodactyly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1055. en:prader-willi syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:prader-willi syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1056. en:prekallikrein deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:prekallikrein deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1057. en:premature aging syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:premature aging syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1058. en:presentey anomaly --- r_associated #0: 20 --> en:leucinosis
    n1=en:presentey anomaly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1059. en:prickle1-related progressive myoclonus epilepsy with ataxia --- r_associated #0: 20 --> en:leucinosis
    n1=en:prickle1-related progressive myoclonus epilepsy with ataxia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1060. en:primary carnitine deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:primary carnitine deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1061. en:primary hyperoxaluria --- r_associated #0: 20 --> en:leucinosis
    n1=en:primary hyperoxaluria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1062. en:primary hypertrophic osteoarthropathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:primary hypertrophic osteoarthropathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1063. en:primary lymphedema --- r_associated #0: 20 --> en:leucinosis
    n1=en:primary lymphedema | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1064. en:primary progressive aphasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:primary progressive aphasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1065. en:profound intellectual disabilities --- r_associated #0: 20 --> en:leucinosis
    n1=en:profound intellectual disabilities | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1066. en:progeria --- r_associated #0: 20 --> en:leucinosis
    n1=en:progeria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1067. en:progressive bulbar palsy --- r_associated #0: 20 --> en:leucinosis
    n1=en:progressive bulbar palsy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1068. en:progressive muscular atrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:progressive muscular atrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1069. en:progressive supranuclear palsy --- r_associated #0: 20 --> en:leucinosis
    n1=en:progressive supranuclear palsy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1070. en:prolidase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:prolidase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1071. en:prolonged electroretinal response suppression --- r_associated #0: 20 --> en:leucinosis
    n1=en:prolonged electroretinal response suppression | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1072. en:propionic acidemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:propionic acidemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1073. en:prosopagnosia --- r_associated #0: 20 --> en:leucinosis
    n1=en:prosopagnosia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1074. en:prostate cancer, familial --- r_associated #0: 20 --> en:leucinosis
    n1=en:prostate cancer, familial | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1075. en:proteus syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:proteus syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1076. en:prune belly syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:prune belly syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1077. en:pseudoachondroplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:pseudoachondroplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1078. en:pseudocholinesterase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:pseudocholinesterase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1079. en:pseudohermaphroditism --- r_associated #0: 20 --> en:leucinosis
    n1=en:pseudohermaphroditism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1080. en:pseudohypoaldosteronism --- r_associated #0: 20 --> en:leucinosis
    n1=en:pseudohypoaldosteronism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1081. en:pseudohypoaldosteronism, type 1, recessive form --- r_associated #0: 20 --> en:leucinosis
    n1=en:pseudohypoaldosteronism, type 1, recessive form | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1082. en:pseudohypoparathyroidism --- r_associated #0: 20 --> en:leucinosis
    n1=en:pseudohypoparathyroidism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1083. en:pseudotrisomy 13 syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1084. en:pseudotumor cerebri --- r_associated #0: 20 --> en:leucinosis
    n1=en:pseudotumor cerebri | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1085. en:pseudoxanthoma elasticum --- r_associated #0: 20 --> en:leucinosis
    n1=en:pseudoxanthoma elasticum | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1086. en:psychology qualifier --- r_associated #0: 20 --> en:leucinosis
    n1=en:psychology qualifier | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1087. en:pulmonary alveolar proteinosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:pulmonary alveolar proteinosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1088. en:purine-nucleoside phosphorylase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:purine-nucleoside phosphorylase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1089. en:purine-pyrimidine metabolism, inborn errors --- r_associated #0: 20 --> en:leucinosis
    n1=en:purine-pyrimidine metabolism, inborn errors | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1090. en:pyle metaphyseal dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:pyle metaphyseal dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1091. en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 --- r_associated #0: 20 --> en:leucinosis
    n1=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1092. en:pyridoxine dependency syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:pyridoxine dependency syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1093. en:pyruvate carboxylase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:pyruvate carboxylase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1094. en:pyruvate dehydrogenase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:pyruvate dehydrogenase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1095. en:pyruvate kinase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:pyruvate kinase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1096. en:radial aplasia-thrombocytopenia syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:radial aplasia-thrombocytopenia syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1097. en:radiotherapeutic --- r_associated #0: 20 --> en:leucinosis
    n1=en:radiotherapeutic | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1098. en:radioulnar synostosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:radioulnar synostosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1099. en:rapadilino syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:rapadilino syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1100. en:reardon hall slaney syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:reardon hall slaney syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1101. en:refsum disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:refsum disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1102. en:rehabilitation aspects --- r_associated #0: 20 --> en:leucinosis
    n1=en:rehabilitation aspects | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1103. en:renal aminoacidurias --- r_associated #0: 20 --> en:leucinosis
    n1=en:renal aminoacidurias | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1104. en:renal tubular transport, inborn errors --- r_associated #0: 20 --> en:leucinosis
    n1=en:renal tubular transport, inborn errors | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1105. en:renal tubulopathy with encephalopathy and liver failure syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:renal tubulopathy with encephalopathy and liver failure syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1106. en:renpenning syndrome 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:renpenning syndrome 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1107. en:retinitis pigmentosa --- r_associated #0: 20 --> en:leucinosis
    n1=en:retinitis pigmentosa | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1108. en:retinitis punctata albescens (disorder) --- r_associated #0: 20 --> en:leucinosis
    n1=en:retinitis punctata albescens (disorder) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1109. en:retinoblastoma --- r_associated #0: 20 --> en:leucinosis
    n1=en:retinoblastoma | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1110. en:retinoschisis --- r_associated #0: 20 --> en:leucinosis
    n1=en:retinoschisis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1111. en:rett syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:rett syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1112. en:rett syndrome, atypical --- r_associated #0: 20 --> en:leucinosis
    n1=en:rett syndrome, atypical | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1113. en:revesz syndrome (disorder) --- r_associated #0: 20 --> en:leucinosis
    n1=en:revesz syndrome (disorder) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1114. en:rhabdoid tumor predisposition syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:rhabdoid tumor predisposition syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1115. en:rhizomelic dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:rhizomelic dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1116. en:richards-rundle syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:richards-rundle syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1117. en:rieger syndrome type 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:rieger syndrome type 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1118. en:rna polymerase iii-related leukodystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:rna polymerase iii-related leukodystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1119. en:roberts syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:roberts syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1120. en:robinow syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:robinow syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1121. en:roentgenographic --- r_associated #0: 20 --> en:leucinosis
    n1=en:roentgenographic | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1122. en:rothmund-thomson syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:rothmund-thomson syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1123. en:russell-silver syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:russell-silver syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1124. en:saito kuba tsuruta syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:saito kuba tsuruta syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1125. en:sanfilippo syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:sanfilippo syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1126. en:sarcosinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:sarcosinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1127. en:savant syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:savant syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1128. en:schinzel-giedion midface-retraction syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:schinzel-giedion midface-retraction syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1129. en:schwannomatosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:schwannomatosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1130. en:scimitar syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:scimitar syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1131. en:scleredema adultorum --- r_associated #0: 20 --> en:leucinosis
    n1=en:scleredema adultorum | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1132. en:scleromyxedema --- r_associated #0: 20 --> en:leucinosis
    n1=en:scleromyxedema | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1133. en:sea-blue histiocyte syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:sea-blue histiocyte syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1134. en:seckel syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:seckel syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1135. en:seizure --- r_associated #0: 20 --> en:leucinosis
    n1=en:seizure | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1136. en:selective antibody deficiency with normal immunoglobulins --- r_associated #0: 20 --> en:leucinosis
    n1=en:selective antibody deficiency with normal immunoglobulins | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1137. en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis --- r_associated #0: 20 --> en:leucinosis
    n1=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1138. en:septo-optic dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:septo-optic dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1139. en:severe early childhood onset retinal dystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:severe early childhood onset retinal dystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1140. en:severe mental retardation (i.q. 20-34) --- r_associated #0: 20 --> en:leucinosis
    n1=en:severe mental retardation (i.q. 20-34) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1141. en:severe steroid 21-hydroxylase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:severe steroid 21-hydroxylase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1142. en:sex chromosome disorders --- r_associated #0: 20 --> en:leucinosis
    n1=en:sex chromosome disorders | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1143. en:short rib-polydactyly syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:short rib-polydactyly syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1144. en:short stature homeobox deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:short stature homeobox deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1145. en:shprintzen-goldberg craniosynostosis syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:shprintzen-goldberg craniosynostosis syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1146. en:shwachman-diamond syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:shwachman-diamond syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1147. en:shy-drager syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:shy-drager syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1148. en:sickle cell disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:sickle cell disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1149. en:simpson golabi behmel syndrome type 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:simpson golabi behmel syndrome type 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1150. en:sinus histiocytosis with massive lymphadenopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:sinus histiocytosis with massive lymphadenopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1151. en:sitosterolemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:sitosterolemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1152. en:sitosterolemia with xanthomatosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:sitosterolemia with xanthomatosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1153. en:sjogren-larsson syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:sjogren-larsson syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1154. en:sly syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:sly syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1155. en:smith-lemli-opitz syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:smith-lemli-opitz syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1156. en:smith-magenis syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:smith-magenis syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1157. en:smith-mccort dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:smith-mccort dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1158. en:sonoda syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:sonoda syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1159. en:sotos syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:sotos syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1160. en:spasmodic torticollis --- r_associated #0: 20 --> en:leucinosis
    n1=en:spasmodic torticollis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1161. en:spastic ataxia, charlevoix-saguenay type --- r_associated #0: 20 --> en:leucinosis
    n1=en:spastic ataxia, charlevoix-saguenay type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1162. en:spastic paraplegia 15, autosomal recessive --- r_associated #0: 20 --> en:leucinosis
    n1=en:spastic paraplegia 15, autosomal recessive | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1163. en:specific enzyme deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:specific enzyme deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1164. en:spinal muscular atrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:spinal muscular atrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1165. en:spinal muscular atrophy with respiratory distress 1 --- r_associated #0: 20 --> en:leucinosis
    n1=en:spinal muscular atrophy with respiratory distress 1 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1166. en:spinocerebellar ataxia with epilepsy --- r_associated #0: 20 --> en:leucinosis
    n1=en:spinocerebellar ataxia with epilepsy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1167. en:spinocerebellar ataxia, autosomal recessive 2 --- r_associated #0: 20 --> en:leucinosis
    n1=en:spinocerebellar ataxia, autosomal recessive 2 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1168. en:spondylo-ocular syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:spondylo-ocular syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1169. en:spondylocarpotarsal synostosis syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:spondylocarpotarsal synostosis syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1170. en:spondyloenchondrodysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:spondyloenchondrodysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1171. en:spondyloenchondrodysplasia with immune dysregulation --- r_associated #0: 20 --> en:leucinosis
    n1=en:spondyloenchondrodysplasia with immune dysregulation | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1172. en:spondyloepimetaphyseal dysplasia with joint laxity type 2 --- r_associated #0: 20 --> en:leucinosis
    n1=en:spondyloepimetaphyseal dysplasia with joint laxity type 2 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1173. en:spondyloepimetaphyseal dysplasia, sponastrime type --- r_associated #0: 20 --> en:leucinosis
    n1=en:spondyloepimetaphyseal dysplasia, sponastrime type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1174. en:spondyloepiphyseal dysplasia tarda, toledo type --- r_associated #0: 20 --> en:leucinosis
    n1=en:spondyloepiphyseal dysplasia tarda, toledo type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1175. en:spondyloepiphyseal dysplasia, omani type --- r_associated #0: 20 --> en:leucinosis
    n1=en:spondyloepiphyseal dysplasia, omani type | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1176. en:staphylococcal scalded skin syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:staphylococcal scalded skin syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1177. en:stargardt disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:stargardt disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1178. en:status epilepticus --- r_associated #0: 20 --> en:leucinosis
    n1=en:status epilepticus | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1179. en:steroid metabolism, inborn errors --- r_associated #0: 20 --> en:leucinosis
    n1=en:steroid metabolism, inborn errors | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1180. en:stickler syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:stickler syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1181. en:stiff person syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:stiff person syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1182. en:stiff skin syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:stiff skin syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1183. en:storage disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:storage disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1184. en:subacute sclerosing panencephalitis --- r_associated #0: 20 --> en:leucinosis
    n1=en:subacute sclerosing panencephalitis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1185. en:succinic semialdehyde dehydrogenase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:succinic semialdehyde dehydrogenase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1186. en:sudden infant death with dysgenesis of the testes syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:sudden infant death with dysgenesis of the testes syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1187. en:sudden unexplained death in childhood --- r_associated #0: 20 --> en:leucinosis
    n1=en:sudden unexplained death in childhood | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1188. en:sudden unexplained infant death --- r_associated #0: 20 --> en:leucinosis
    n1=en:sudden unexplained infant death | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1189. en:sulfite oxidase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:sulfite oxidase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1190. en:sunct syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:sunct syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1191. en:superior mesenteric artery syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:superior mesenteric artery syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1192. en:surfactant protein deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:surfactant protein deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1193. en:surgical aspects --- r_associated #0: 20 --> en:leucinosis
    n1=en:surgical aspects | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1194. en:sweet syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:sweet syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1195. en:swyer james syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:swyer james syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1196. en:syndrome of apparent mineralocorticoid excess --- r_associated #0: 20 --> en:leucinosis
    n1=en:syndrome of apparent mineralocorticoid excess | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1197. en:synpolydactyly --- r_associated #0: 20 --> en:leucinosis
    n1=en:synpolydactyly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1198. en:syringomyelia --- r_associated #0: 20 --> en:leucinosis
    n1=en:syringomyelia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1199. en:takotsubo cardiomyopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:takotsubo cardiomyopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1200. en:tangier disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:tangier disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1201. en:taxonomic --- r_associated #0: 20 --> en:leucinosis
    n1=en:taxonomic | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1202. en:tay-sachs disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:tay-sachs disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1203. en:tetra-amelia autosomal recessive --- r_associated #0: 20 --> en:leucinosis
    n1=en:tetra-amelia autosomal recessive | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1204. en:tetraamelia multiple malformations --- r_associated #0: 20 --> en:leucinosis
    n1=en:tetraamelia multiple malformations | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1205. en:thanatophoric dysplasia --- r_associated #0: 20 --> en:leucinosis
    n1=en:thanatophoric dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1206. en:therapeutic aspects --- r_associated #0: 20 --> en:leucinosis
    n1=en:therapeutic aspects | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1207. en:thomas syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:thomas syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1208. en:thoracic outlet syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:thoracic outlet syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1209. en:thrombocytopenia 2 --- r_associated #0: 20 --> en:leucinosis
    n1=en:thrombocytopenia 2 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1210. en:thyroid dysgenesis --- r_associated #0: 20 --> en:leucinosis
    n1=en:thyroid dysgenesis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1211. en:thyroid dyshormonogenesis 4 --- r_associated #0: 20 --> en:leucinosis
    n1=en:thyroid dyshormonogenesis 4 | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1212. en:thyroid hormone resistance syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:thyroid hormone resistance syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1213. en:tiglic acidemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:tiglic acidemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1214. en:tmem70 related mitochondrial encephalo-cardio-myopathy --- r_associated #0: 20 --> en:leucinosis
    n1=en:tmem70 related mitochondrial encephalo-cardio-myopathy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1215. en:togaviridae infection --- r_associated #0: 20 --> en:leucinosis
    n1=en:togaviridae infection | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1216. en:tolosa-hunt syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:tolosa-hunt syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1217. en:tooth and nail syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:tooth and nail syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1218. en:tracheobronchomalacia --- r_associated #0: 20 --> en:leucinosis
    n1=en:tracheobronchomalacia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1219. en:tracheobronchomegaly --- r_associated #0: 20 --> en:leucinosis
    n1=en:tracheobronchomegaly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1220. en:transcobalamin ii deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:transcobalamin ii deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1221. en:transient global amnesia --- r_associated #0: 20 --> en:leucinosis
    n1=en:transient global amnesia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1222. en:transitory amino acid metabolic disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:transitory amino acid metabolic disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1223. en:transposition of great vessels --- r_associated #0: 20 --> en:leucinosis
    n1=en:transposition of great vessels | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1224. en:treacher collins syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:treacher collins syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1225. en:trichinosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:trichinosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1226. en:trichohepatoenteric syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:trichohepatoenteric syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1227. en:trichorhinophalangeal syndrome type i --- r_associated #0: 20 --> en:leucinosis
    n1=en:trichorhinophalangeal syndrome type i | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1228. en:trichorhinophalangeal syndrome type ii --- r_associated #0: 20 --> en:leucinosis
    n1=en:trichorhinophalangeal syndrome type ii | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1229. en:trichothiodystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:trichothiodystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1230. en:trigger finger disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:trigger finger disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1231. en:triploidy syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:triploidy syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1232. en:trisomy 10p --- r_associated #0: 20 --> en:leucinosis
    n1=en:trisomy 10p | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1233. en:trisomy 14 mosaicism --- r_associated #0: 20 --> en:leucinosis
    n1=en:trisomy 14 mosaicism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1234. en:true hermaphroditism --- r_associated #0: 20 --> en:leucinosis
    n1=en:true hermaphroditism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1235. en:tuberculosis of meninges (cerebral)(spinal) --- r_associated #0: 20 --> en:leucinosis
    n1=en:tuberculosis of meninges (cerebral)(spinal) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1236. en:tuberous sclerosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:tuberous sclerosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1237. en:tungland bellman syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:tungland bellman syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1238. en:turner syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:turner syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1239. en:tylosis with esophageal cancer --- r_associated #0: 20 --> en:leucinosis
    n1=en:tylosis with esophageal cancer | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1240. en:type ii acrocephalopolysyndactyly --- r_associated #0: 20 --> en:leucinosis
    n1=en:type ii acrocephalopolysyndactyly | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1241. en:tyrosinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:tyrosinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1242. en:tyrosinemia type ii --- r_associated #0: 20 --> en:leucinosis
    n1=en:tyrosinemia type ii | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1243. en:tyrosinemia, type iii --- r_associated #0: 20 --> en:leucinosis
    n1=en:tyrosinemia, type iii | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1244. en:ugt1a1*28 polymorphism --- r_associated #0: 20 --> en:leucinosis
    n1=en:ugt1a1*28 polymorphism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1245. en:unclassified metabolic disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:unclassified metabolic disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1246. en:uniparental disomy --- r_associated #0: 20 --> en:leucinosis
    n1=en:uniparental disomy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1247. en:unspecified mental retardation; other impairments of behaviour --- r_associated #0: 20 --> en:leucinosis
    n1=en:unspecified mental retardation; other impairments of behaviour | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1248. en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment --- r_associated #0: 20 --> en:leucinosis
    n1=en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1249. en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour --- r_associated #0: 20 --> en:leucinosis
    n1=en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1250. en:unspecified mental retardation; without mention of impairment of behaviour --- r_associated #0: 20 --> en:leucinosis
    n1=en:unspecified mental retardation; without mention of impairment of behaviour | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1251. en:upper limb defect with eye and ear abnormalities syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:upper limb defect with eye and ear abnormalities syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1252. en:urea cycle metabolism disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:urea cycle metabolism disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1253. en:urine --- r_associated #0: 20 --> en:leucinosis
    n1=en:urine | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1254. en:urine odor, maple syrup --- r_associated #0: 20 --> en:leucinosis
    n1=en:urine odor, maple syrup | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1255. en:urocanase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:urocanase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1256. en:use of ultrasonography --- r_associated #0: 20 --> en:leucinosis
    n1=en:use of ultrasonography | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1257. en:usher syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:usher syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1258. en:uv-sensitive syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:uv-sensitive syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1259. en:uveomeningoencephalitic syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:uveomeningoencephalitic syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1260. en:valinemia --- r_associated #0: 20 --> en:leucinosis
    n1=en:valinemia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1261. en:van der woude syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:van der woude syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1262. en:variegate porphyria --- r_associated #0: 20 --> en:leucinosis
    n1=en:variegate porphyria | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1263. en:verloes bourguignon syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:verloes bourguignon syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1264. en:very long-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:very long-chain acyl-coa dehydrogenase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1265. en:veterinary aspects --- r_associated #0: 20 --> en:leucinosis
    n1=en:veterinary aspects | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1266. en:viruses --- r_associated #0: 20 --> en:leucinosis
    n1=en:viruses | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1267. en:vitelliform macular dystrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:vitelliform macular dystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1268. en:vomiting --- r_associated #0: 20 --> en:leucinosis
    n1=en:vomiting | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1269. en:von hippel-lindau syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:von hippel-lindau syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1270. en:von willebrand disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:von willebrand disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1271. en:waardenburg anophthalmia syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:waardenburg anophthalmia syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1272. en:waardenburg syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:waardenburg syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1273. en:waisman syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:waisman syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1274. en:walker-warburg syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:walker-warburg syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1275. en:wallerian degeneration --- r_associated #0: 20 --> en:leucinosis
    n1=en:wallerian degeneration | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1276. en:wandering spleen --- r_associated #0: 20 --> en:leucinosis
    n1=en:wandering spleen | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1277. en:warsaw breakage syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:warsaw breakage syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1278. en:waterhouse-friderichsen syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:waterhouse-friderichsen syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1279. en:weaver syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:weaver syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1280. en:wegener granulomatosis --- r_associated #0: 20 --> en:leucinosis
    n1=en:wegener granulomatosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1281. en:weill-marchesani syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:weill-marchesani syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1282. en:werdnig-hoffmann disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:werdnig-hoffmann disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1283. en:werner syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:werner syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1284. en:west syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:west syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1285. en:whipple disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:whipple disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1286. en:white matter signal abnormalities in various brain regions --- r_associated #0: 20 --> en:leucinosis
    n1=en:white matter signal abnormalities in various brain regions | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1287. en:williams syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:williams syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1288. en:wilms tumor --- r_associated #0: 20 --> en:leucinosis
    n1=en:wilms tumor | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1289. en:wiskott-aldrich syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:wiskott-aldrich syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1290. en:wolf-hirschhorn syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:wolf-hirschhorn syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1291. en:wolfram syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:wolfram syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1292. en:wolman disease --- r_associated #0: 20 --> en:leucinosis
    n1=en:wolman disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1293. en:worldwide incidence of 1 in 185,000 live births --- r_associated #0: 20 --> en:leucinosis
    n1=en:worldwide incidence of 1 in 185,000 live births | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1294. en:wt limb blood syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:wt limb blood syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1295. en:x-linked bulbar-muscular atrophy --- r_associated #0: 20 --> en:leucinosis
    n1=en:x-linked bulbar-muscular atrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1296. en:x-linked creatine transporter deficiency --- r_associated #0: 20 --> en:leucinosis
    n1=en:x-linked creatine transporter deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1297. en:x-linked dominant hypophosphatemic rickets --- r_associated #0: 20 --> en:leucinosis
    n1=en:x-linked dominant hypophosphatemic rickets | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1298. en:x-linked hypophosphatemic rickets --- r_associated #0: 20 --> en:leucinosis
    n1=en:x-linked hypophosphatemic rickets | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1299. en:x-linked inherited disorder --- r_associated #0: 20 --> en:leucinosis
    n1=en:x-linked inherited disorder | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1300. en:xanthinuria, type i --- r_associated #0: 20 --> en:leucinosis
    n1=en:xanthinuria, type i | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1301. en:xeroderma pigmentosum --- r_associated #0: 20 --> en:leucinosis
    n1=en:xeroderma pigmentosum | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1302. en:xerophthalmia --- r_associated #0: 20 --> en:leucinosis
    n1=en:xerophthalmia | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1303. en:xxxy and xxxxy syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:xxxy and xxxxy syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1304. en:xyy syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:xyy syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1305. en:yellow nail syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:yellow nail syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1306. en:zellweger syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=en:zellweger syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1307. eu en milieu de jet --- r_associated #0: 20 --> en:leucinosis
    n1=eu en milieu de jet | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1308. gène --- r_associated #0: 20 --> en:leucinosis
    n1=gène | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1309. handicap --- r_associated #0: 20 --> en:leucinosis
    n1=handicap | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1310. homocystinurie --- r_associated #0: 20 --> en:leucinosis
    n1=homocystinurie | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1311. hyperleucinémie --- r_associated #0: 20 --> en:leucinosis
    n1=hyperleucinémie | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1312. hypogonadisme avec anosmie --- r_associated #0: 20 --> en:leucinosis
    n1=hypogonadisme avec anosmie | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1313. hémoglobinopathie à hématies falciformes --- r_associated #0: 20 --> en:leucinosis
    n1=hémoglobinopathie à hématies falciformes | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1314. hémoglobinose S --- r_associated #0: 20 --> en:leucinosis
    n1=hémoglobinose S | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1315. hémoglobinose ss --- r_associated #0: 20 --> en:leucinosis
    n1=hémoglobinose ss | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1316. isoleucine --- r_associated #0: 20 --> en:leucinosis
    n1=isoleucine | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1317. leucine --- r_associated #0: 20 --> en:leucinosis
    n1=leucine | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1318. leucinose aiguë --- r_associated #0: 20 --> en:leucinosis
    n1=leucinose aiguë | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1319. leucinose classique --- r_associated #0: 20 --> en:leucinosis
    n1=leucinose classique | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1320. leucinose intermittente --- r_associated #0: 20 --> en:leucinosis
    n1=leucinose intermittente | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1321. leucinose intermédiaire --- r_associated #0: 20 --> en:leucinosis
    n1=leucinose intermédiaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1322. leucinose thiamine-sensible --- r_associated #0: 20 --> en:leucinosis
    n1=leucinose thiamine-sensible | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1323. leucinoses --- r_associated #0: 20 --> en:leucinosis
    n1=leucinoses | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1324. maladie --- r_associated #0: 20 --> en:leucinosis
    n1=maladie | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1325. maladie de Seitelberger --- r_associated #0: 20 --> en:leucinosis
    n1=maladie de Seitelberger | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1326. maladie des urines à odeur de sirop d'érable --- r_associated #0: 20 --> en:leucinosis
    n1=maladie des urines à odeur de sirop d'érable | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1327. maladie des urines à odeur de sirop d'érable, forme classique --- r_associated #0: 20 --> en:leucinosis
    n1=maladie des urines à odeur de sirop d'érable, forme classique | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1328. maladie drépanocytaire --- r_associated #0: 20 --> en:leucinosis
    n1=maladie drépanocytaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1329. maladie du $organe$ --- r_associated #0: 20 --> en:leucinosis
    n1=maladie du $organe$ | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1330. maladie génétique --- r_associated #0: 20 --> en:leucinosis
    n1=maladie génétique | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1331. maladie génétique congénitale --- r_associated #0: 20 --> en:leucinosis
    n1=maladie génétique congénitale | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1332. maladie génétique du métabolisme des acides aminés --- r_associated #0: 20 --> en:leucinosis
    n1=maladie génétique du métabolisme des acides aminés | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1333. maladie rare --- r_associated #0: 20 --> en:leucinosis
    n1=maladie rare | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1334. maladie
    (médecine)
     --- r_associated #0: 20 --> en:leucinosis
    n1=maladie
    (médecine)
    | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1335. maladie
    (médecine, vétérinaire)
     --- r_associated #0: 20 --> en:leucinosis
    n1=maladie
    (médecine, vétérinaire)
    | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1336. maladie
    (végétaux)
     --- r_associated #0: 20 --> en:leucinosis
    n1=maladie
    (végétaux)
    | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1337. maladies --- r_associated #0: 20 --> en:leucinosis
    n1=maladies | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1338. maladies des urines avec odeur de sirop erable --- r_associated #0: 20 --> en:leucinosis
    n1=maladies des urines avec odeur de sirop erable | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1339. maladies du sirop d'erable --- r_associated #0: 20 --> en:leucinosis
    n1=maladies du sirop d'erable | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1340. maladies génétiques du métabolisme des acides aminés --- r_associated #0: 20 --> en:leucinosis
    n1=maladies génétiques du métabolisme des acides aminés | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1341. maladies rares --- r_associated #0: 20 --> en:leucinosis
    n1=maladies rares | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1342. monilethrix --- r_associated #0: 20 --> en:leucinosis
    n1=monilethrix | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1343. médecine --- r_associated #0: 20 --> en:leucinosis
    n1=médecine | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1344. médecine
    (science)
     --- r_associated #0: 20 --> en:leucinosis
    n1=médecine
    (science)
    | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1345. non précisée, anémie drépanocytaire --- r_associated #0: 20 --> en:leucinosis
    n1=non précisée, anémie drépanocytaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1346. opisthotonos --- r_associated #0: 20 --> en:leucinosis
    n1=opisthotonos | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1347. pathologie --- r_associated #0: 20 --> en:leucinosis
    n1=pathologie | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1348. phénylcétonurie --- r_associated #0: 20 --> en:leucinosis
    n1=phénylcétonurie | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1349. processus pathologique --- r_associated #0: 20 --> en:leucinosis
    n1=processus pathologique | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1350. rétinoblastome héréditaire --- r_associated #0: 20 --> en:leucinosis
    n1=rétinoblastome héréditaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1351. sicklémie --- r_associated #0: 20 --> en:leucinosis
    n1=sicklémie | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1352. sirop --- r_associated #0: 20 --> en:leucinosis
    n1=sirop | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1353. sirop d'érable --- r_associated #0: 20 --> en:leucinosis
    n1=sirop d'érable | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1354. syndrome de Beauvieux --- r_associated #0: 20 --> en:leucinosis
    n1=syndrome de Beauvieux | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1355. syndrome de Hartnup --- r_associated #0: 20 --> en:leucinosis
    n1=syndrome de Hartnup | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1356. syndrome des histiocytes bleu marine --- r_associated #0: 20 --> en:leucinosis
    n1=syndrome des histiocytes bleu marine | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1357. tuberculose des méninges --- r_associated #0: 20 --> en:leucinosis
    n1=tuberculose des méninges | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1358. urine --- r_associated #0: 20 --> en:leucinosis
    n1=urine | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1359. valine --- r_associated #0: 20 --> en:leucinosis
    n1=valine | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1360. yellow nail syndrome --- r_associated #0: 20 --> en:leucinosis
    n1=yellow nail syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1361. érable --- r_associated #0: 20 --> en:leucinosis
    n1=érable | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1362. Décarboxylase --- r_associated #0: 15 --> en:leucinosis
    n1=Décarboxylase | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1363. Kallman --- r_associated #0: 15 --> en:leucinosis
    n1=Kallman | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1364. aclasie diaphysaire --- r_associated #0: 15 --> en:leucinosis
    n1=aclasie diaphysaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1365. anémie falciforme --- r_associated #0: 15 --> en:leucinosis
    n1=anémie falciforme | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1366. chondrodysplasie héréditaire déformante --- r_associated #0: 15 --> en:leucinosis
    n1=chondrodysplasie héréditaire déformante | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1367. chorée héréditaire --- r_associated #0: 15 --> en:leucinosis
    n1=chorée héréditaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1368. coarctation aortique --- r_associated #0: 15 --> en:leucinosis
    n1=coarctation aortique | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1369. craniosynostose --- r_associated #0: 15 --> en:leucinosis
    n1=craniosynostose | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1370. crânio-sténose --- r_associated #0: 15 --> en:leucinosis
    n1=crânio-sténose | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1371. cysticercose cérébrale --- r_associated #0: 15 --> en:leucinosis
    n1=cysticercose cérébrale | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1372. cysticercose du système nerveux central --- r_associated #0: 15 --> en:leucinosis
    n1=cysticercose du système nerveux central | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1373. cysticercose neurologique --- r_associated #0: 15 --> en:leucinosis
    n1=cysticercose neurologique | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1374. drépanocytose --- r_associated #0: 15 --> en:leucinosis
    n1=drépanocytose | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1375. exostose héréditaire multiple --- r_associated #0: 15 --> en:leucinosis
    n1=exostose héréditaire multiple | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1376. hyperoxalurie primitive --- r_associated #0: 15 --> en:leucinosis
    n1=hyperoxalurie primitive | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1377. hypophosphatasie --- r_associated #0: 15 --> en:leucinosis
    n1=hypophosphatasie | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1378. lymphome malin diffus --- r_associated #0: 15 --> en:leucinosis
    n1=lymphome malin diffus | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1379. lymphome à cellules b --- r_associated #0: 15 --> en:leucinosis
    n1=lymphome à cellules b | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1380. maladie de Whipple --- r_associated #0: 15 --> en:leucinosis
    n1=maladie de Whipple | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1381. malformation d'Arnold-Chiari --- r_associated #0: 15 --> en:leucinosis
    n1=malformation d'Arnold-Chiari | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1382. ptose splénique --- r_associated #0: 15 --> en:leucinosis
    n1=ptose splénique | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1383. rate ectopique --- r_associated #0: 15 --> en:leucinosis
    n1=rate ectopique | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1384. rate errante --- r_associated #0: 15 --> en:leucinosis
    n1=rate errante | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1385. syndrome de Kallman-de Morsier --- r_associated #0: 15 --> en:leucinosis
    n1=syndrome de Kallman-de Morsier | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1386. syndrome de de Morsier-Kallmann --- r_associated #0: 15 --> en:leucinosis
    n1=syndrome de de Morsier-Kallmann | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1387. syndrome de soto --- r_associated #0: 15 --> en:leucinosis
    n1=syndrome de soto | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1388. troubles héréditaires du transport tubulaire rénal --- r_associated #0: 15 --> en:leucinosis
    n1=troubles héréditaires du transport tubulaire rénal | n2=en:leucinosis | rel=r_associated | relid=0 | w=15
  1389. Cérumen --- r_associated #0: 10 --> en:leucinosis
    n1=Cérumen | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1390. Goltz --- r_associated #0: 10 --> en:leucinosis
    n1=Goltz | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1391. HELLP syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=HELLP syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1392. Homocystinurie --- r_associated #0: 10 --> en:leucinosis
    n1=Homocystinurie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1393. Isoleucine --- r_associated #0: 10 --> en:leucinosis
    n1=Isoleucine | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1394. Malformation d'Arnold-Chiari --- r_associated #0: 10 --> en:leucinosis
    n1=Malformation d'Arnold-Chiari | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1395. Phénylcétonurie --- r_associated #0: 10 --> en:leucinosis
    n1=Phénylcétonurie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1396. Syndrome de Mayer-Rokitansky-Küster-Hauser --- r_associated #0: 10 --> en:leucinosis
    n1=Syndrome de Mayer-Rokitansky-Küster-Hauser | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1397. Valine --- r_associated #0: 10 --> en:leucinosis
    n1=Valine | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1398. a-bêta-lipoprotéinémie --- r_associated #0: 10 --> en:leucinosis
    n1=a-bêta-lipoprotéinémie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1399. achromatopsie --- r_associated #0: 10 --> en:leucinosis
    n1=achromatopsie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1400. acromégalie --- r_associated #0: 10 --> en:leucinosis
    n1=acromégalie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1401. ainhum --- r_associated #0: 10 --> en:leucinosis
    n1=ainhum | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1402. albinisme --- r_associated #0: 10 --> en:leucinosis
    n1=albinisme | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1403. anasarque --- r_associated #0: 10 --> en:leucinosis
    n1=anasarque | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1404. anencéphalie --- r_associated #0: 10 --> en:leucinosis
    n1=anencéphalie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1405. anomalie chromosomique --- r_associated #0: 10 --> en:leucinosis
    n1=anomalie chromosomique | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1406. anormalité des chromosomes --- r_associated #0: 10 --> en:leucinosis
    n1=anormalité des chromosomes | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1407. aphasie primaire progressive --- r_associated #0: 10 --> en:leucinosis
    n1=aphasie primaire progressive | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1408. aphasies primaires progressives --- r_associated #0: 10 --> en:leucinosis
    n1=aphasies primaires progressives | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1409. aprosencéphalie --- r_associated #0: 10 --> en:leucinosis
    n1=aprosencéphalie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1410. arachnodactylie --- r_associated #0: 10 --> en:leucinosis
    n1=arachnodactylie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1411. arthrogrypose --- r_associated #0: 10 --> en:leucinosis
    n1=arthrogrypose | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1412. atrophie olivopontocérébelleuse --- r_associated #0: 10 --> en:leucinosis
    n1=atrophie olivopontocérébelleuse | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1413. aïnhum --- r_associated #0: 10 --> en:leucinosis
    n1=aïnhum | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1414. cataplexie --- r_associated #0: 10 --> en:leucinosis
    n1=cataplexie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1415. chondrodysplasia punctata --- r_associated #0: 10 --> en:leucinosis
    n1=chondrodysplasia punctata | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1416. chondrodysplasie déformante héréditaire --- r_associated #0: 10 --> en:leucinosis
    n1=chondrodysplasie déformante héréditaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1417. chorée de Huntington --- r_associated #0: 10 --> en:leucinosis
    n1=chorée de Huntington | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1418. crâniosténose --- r_associated #0: 10 --> en:leucinosis
    n1=crâniosténose | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1419. crâniosynostose --- r_associated #0: 10 --> en:leucinosis
    n1=crâniosynostose | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1420. cutis laxa --- r_associated #0: 10 --> en:leucinosis
    n1=cutis laxa | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1421. dentinogenesis imperfecta --- r_associated #0: 10 --> en:leucinosis
    n1=dentinogenesis imperfecta | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1422. diabète bronzé --- r_associated #0: 10 --> en:leucinosis
    n1=diabète bronzé | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1423. dystrophie musculaire --- r_associated #0: 10 --> en:leucinosis
    n1=dystrophie musculaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1424. déficit en cytochrome oxydase --- r_associated #0: 10 --> en:leucinosis
    n1=déficit en cytochrome oxydase | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1425. en:Albright's hereditary osteodystrophy --- r_associated #0: 10 --> en:leucinosis
    n1=en:Albright's hereditary osteodystrophy | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1426. en:Bartter syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:Bartter syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1427. en:Carney complex --- r_associated #0: 10 --> en:leucinosis
    n1=en:Carney complex | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1428. en:Cogan-Reese syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:Cogan-Reese syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1429. en:Ehlers-Danlos syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:Ehlers-Danlos syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1430. en:Feingold syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:Feingold syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1431. en:Fox-Fordyce disease --- r_associated #0: 10 --> en:leucinosis
    n1=en:Fox-Fordyce disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1432. en:Fraser syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:Fraser syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1433. en:Friedreich ataxia --- r_associated #0: 10 --> en:leucinosis
    n1=en:Friedreich ataxia | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1434. en:Fryns syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:Fryns syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1435. en:Gaucher disease --- r_associated #0: 10 --> en:leucinosis
    n1=en:Gaucher disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1436. en:Goodpasture syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:Goodpasture syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1437. en:Holt-Oram syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:Holt-Oram syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1438. en:Kniest dysplasia --- r_associated #0: 10 --> en:leucinosis
    n1=en:Kniest dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1439. en:LEOPARD syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:LEOPARD syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1440. en:Laron syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:Laron syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1441. en:MELAS syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:MELAS syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1442. en:Marburg virus disease --- r_associated #0: 10 --> en:leucinosis
    n1=en:Marburg virus disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1443. en:Proteus syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:Proteus syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1444. en:Smith-Magenis syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:Smith-Magenis syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1445. en:Stargardt disease --- r_associated #0: 10 --> en:leucinosis
    n1=en:Stargardt disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1446. en:Tangier disease --- r_associated #0: 10 --> en:leucinosis
    n1=en:Tangier disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1447. en:Von Willebrand disease --- r_associated #0: 10 --> en:leucinosis
    n1=en:Von Willebrand disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1448. en:Wegener granulomatosis --- r_associated #0: 10 --> en:leucinosis
    n1=en:Wegener granulomatosis | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1449. en:Weill-Marchesani syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:Weill-Marchesani syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1450. en:Whipple disease --- r_associated #0: 10 --> en:leucinosis
    n1=en:Whipple disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1451. en:Zellweger syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:Zellweger syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1452. en:cerumen --- r_associated #0: 10 --> en:leucinosis
    n1=en:cerumen | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1453. en:chromosome 19 --- r_associated #0: 10 --> en:leucinosis
    n1=en:chromosome 19 | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1454. en:chromosome 7 --- r_associated #0: 10 --> en:leucinosis
    n1=en:chromosome 7 | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1455. en:eds --- r_associated #0: 10 --> en:leucinosis
    n1=en:eds | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1456. en:ehlers danlos syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=en:ehlers danlos syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1457. en:multiple endocrine neoplasia type 2A --- r_associated #0: 10 --> en:leucinosis
    n1=en:multiple endocrine neoplasia type 2A | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1458. en:trichorhinophalangeal syndrome type II --- r_associated #0: 10 --> en:leucinosis
    n1=en:trichorhinophalangeal syndrome type II | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1459. en:valine --- r_associated #0: 10 --> en:leucinosis
    n1=en:valine | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1460. encéphalocèle --- r_associated #0: 10 --> en:leucinosis
    n1=encéphalocèle | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1461. erythromelalgia --- r_associated #0: 10 --> en:leucinosis
    n1=erythromelalgia | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1462. gastroschisis --- r_associated #0: 10 --> en:leucinosis
    n1=gastroschisis | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1463. genu varum --- r_associated #0: 10 --> en:leucinosis
    n1=genu varum | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1464. gigantisme cérébral --- r_associated #0: 10 --> en:leucinosis
    n1=gigantisme cérébral | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1465. glaucome capsulaire --- r_associated #0: 10 --> en:leucinosis
    n1=glaucome capsulaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1466. holoprosencéphalie --- r_associated #0: 10 --> en:leucinosis
    n1=holoprosencéphalie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1467. hydroa vacciniforme --- r_associated #0: 10 --> en:leucinosis
    n1=hydroa vacciniforme | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1468. hypophosphatasie foetale --- r_associated #0: 10 --> en:leucinosis
    n1=hypophosphatasie foetale | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1469. hypophosphatasie infantile --- r_associated #0: 10 --> en:leucinosis
    n1=hypophosphatasie infantile | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1470. hypophosphatasies --- r_associated #0: 10 --> en:leucinosis
    n1=hypophosphatasies | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1471. hypoplasie dermique en aires --- r_associated #0: 10 --> en:leucinosis
    n1=hypoplasie dermique en aires | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1472. hypoplasie dermique focale --- r_associated #0: 10 --> en:leucinosis
    n1=hypoplasie dermique focale | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1473. hémochromatose primitive --- r_associated #0: 10 --> en:leucinosis
    n1=hémochromatose primitive | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1474. hémoglobinopathie --- r_associated #0: 10 --> en:leucinosis
    n1=hémoglobinopathie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1475. incontinentia pigmenti --- r_associated #0: 10 --> en:leucinosis
    n1=incontinentia pigmenti | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1476. laparoschisis --- r_associated #0: 10 --> en:leucinosis
    n1=laparoschisis | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1477. leptoméningite tuberculeuse --- r_associated #0: 10 --> en:leucinosis
    n1=leptoméningite tuberculeuse | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1478. leptospirose --- r_associated #0: 10 --> en:leucinosis
    n1=leptospirose | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1479. lissencéphalie --- r_associated #0: 10 --> en:leucinosis
    n1=lissencéphalie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1480. lymphome --- r_associated #0: 10 --> en:leucinosis
    n1=lymphome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1481. lymphome malin non hodgkinien --- r_associated #0: 10 --> en:leucinosis
    n1=lymphome malin non hodgkinien | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1482. lymphome malin à cellules à noyaux non encochés --- r_associated #0: 10 --> en:leucinosis
    n1=lymphome malin à cellules à noyaux non encochés | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1483. lymphome non hodgkinien --- r_associated #0: 10 --> en:leucinosis
    n1=lymphome non hodgkinien | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1484. lymphomes non hodgkiniens --- r_associated #0: 10 --> en:leucinosis
    n1=lymphomes non hodgkiniens | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1485. maladie de Bessel-Hagen --- r_associated #0: 10 --> en:leucinosis
    n1=maladie de Bessel-Hagen | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1486. maladie de Huntington --- r_associated #0: 10 --> en:leucinosis
    n1=maladie de Huntington | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1487. maladie de Tangier --- r_associated #0: 10 --> en:leucinosis
    n1=maladie de Tangier | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1488. maladie exostosante multiple --- r_associated #0: 10 --> en:leucinosis
    n1=maladie exostosante multiple | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1489. maladie héréditaire --- r_associated #0: 10 --> en:leucinosis
    n1=maladie héréditaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1490. maladie ostéogénique --- r_associated #0: 10 --> en:leucinosis
    n1=maladie ostéogénique | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1491. méningite tuberculeuse --- r_associated #0: 10 --> en:leucinosis
    n1=méningite tuberculeuse | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1492. méningite tuberculeuse examen non précisé --- r_associated #0: 10 --> en:leucinosis
    n1=méningite tuberculeuse examen non précisé | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1493. nevrilème --- r_associated #0: 10 --> en:leucinosis
    n1=nevrilème | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1494. oedème cérébral --- r_associated #0: 10 --> en:leucinosis
    n1=oedème cérébral | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1495. oedème de l'encéphale --- r_associated #0: 10 --> en:leucinosis
    n1=oedème de l'encéphale | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1496. osteogenesis imperfecta --- r_associated #0: 10 --> en:leucinosis
    n1=osteogenesis imperfecta | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1497. ostéogénèse imparfaite --- r_associated #0: 10 --> en:leucinosis
    n1=ostéogénèse imparfaite | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1498. ostéopétrose avec acidose rénale tubulaire --- r_associated #0: 10 --> en:leucinosis
    n1=ostéopétrose avec acidose rénale tubulaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1499. paralysies périodiques familiales --- r_associated #0: 10 --> en:leucinosis
    n1=paralysies périodiques familiales | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1500. piebaldisme --- r_associated #0: 10 --> en:leucinosis
    n1=piebaldisme | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1501. pinta --- r_associated #0: 10 --> en:leucinosis
    n1=pinta | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1502. piébaldisme --- r_associated #0: 10 --> en:leucinosis
    n1=piébaldisme | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1503. progeria --- r_associated #0: 10 --> en:leucinosis
    n1=progeria | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1504. protéinose alvéolaire --- r_associated #0: 10 --> en:leucinosis
    n1=protéinose alvéolaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1505. pseudo-hypoaldostéronisme --- r_associated #0: 10 --> en:leucinosis
    n1=pseudo-hypoaldostéronisme | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1506. pseudohypoaldostéronisme --- r_associated #0: 10 --> en:leucinosis
    n1=pseudohypoaldostéronisme | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1507. pseudohypoparathyroïdisme --- r_associated #0: 10 --> en:leucinosis
    n1=pseudohypoparathyroïdisme | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1508. rate aberrante --- r_associated #0: 10 --> en:leucinosis
    n1=rate aberrante | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1509. rate flottante --- r_associated #0: 10 --> en:leucinosis
    n1=rate flottante | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1510. rate vagabonde --- r_associated #0: 10 --> en:leucinosis
    n1=rate vagabonde | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1511. rétinoschisis --- r_associated #0: 10 --> en:leucinosis
    n1=rétinoschisis | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1512. septo-optic dysplasia --- r_associated #0: 10 --> en:leucinosis
    n1=septo-optic dysplasia | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1513. sirtuine --- r_associated #0: 10 --> en:leucinosis
    n1=sirtuine | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1514. sisi-test --- r_associated #0: 10 --> en:leucinosis
    n1=sisi-test | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1515. sismothérapie --- r_associated #0: 10 --> en:leucinosis
    n1=sismothérapie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1516. splénoptose --- r_associated #0: 10 --> en:leucinosis
    n1=splénoptose | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1517. stiff skin syndrome --- r_associated #0: 10 --> en:leucinosis
    n1=stiff skin syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1518. syndrome de Goltz --- r_associated #0: 10 --> en:leucinosis
    n1=syndrome de Goltz | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1519. syndrome de Mayer-Rokitansky-Küster-Hauser --- r_associated #0: 10 --> en:leucinosis
    n1=syndrome de Mayer-Rokitansky-Küster-Hauser | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1520. syndrome de Rathbun --- r_associated #0: 10 --> en:leucinosis
    n1=syndrome de Rathbun | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1521. syndrome de Rett --- r_associated #0: 10 --> en:leucinosis
    n1=syndrome de Rett | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1522. syndrome de Rokitansky --- r_associated #0: 10 --> en:leucinosis
    n1=syndrome de Rokitansky | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1523. syndrome de Rokitansky-Küster-Hauser --- r_associated #0: 10 --> en:leucinosis
    n1=syndrome de Rokitansky-Küster-Hauser | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1524. syndrome de de Morsier --- r_associated #0: 10 --> en:leucinosis
    n1=syndrome de de Morsier | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1525. syndrome de la selle turcique vide --- r_associated #0: 10 --> en:leucinosis
    n1=syndrome de la selle turcique vide | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1526. syndrome de prédisposition aux tumeurs rhabdoïdes --- r_associated #0: 10 --> en:leucinosis
    n1=syndrome de prédisposition aux tumeurs rhabdoïdes | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1527. syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire --- r_associated #0: 10 --> en:leucinosis
    n1=syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1528. syndrome héréditaire de cancer du sein et de l'ovaire --- r_associated #0: 10 --> en:leucinosis
    n1=syndrome héréditaire de cancer du sein et de l'ovaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1529. syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire --- r_associated #0: 10 --> en:leucinosis
    n1=syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1530. trachéo-bronchomégalie --- r_associated #0: 10 --> en:leucinosis
    n1=trachéo-bronchomégalie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1531. trachéobronchomégalie --- r_associated #0: 10 --> en:leucinosis
    n1=trachéobronchomégalie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1532. tuberculose méningée --- r_associated #0: 10 --> en:leucinosis
    n1=tuberculose méningée | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1533. tumeur de Wilms héréditaire --- r_associated #0: 10 --> en:leucinosis
    n1=tumeur de Wilms héréditaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1534. tumeur stromale gastro-intestinale héréditaire --- r_associated #0: 10 --> en:leucinosis
    n1=tumeur stromale gastro-intestinale héréditaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1535. vomissement --- r_associated #0: 10 --> en:leucinosis
    n1=vomissement | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1536. vomissements --- r_associated #0: 10 --> en:leucinosis
    n1=vomissements | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1537. xeroderma pigmentosum --- r_associated #0: 10 --> en:leucinosis
    n1=xeroderma pigmentosum | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1538. érythermalgie --- r_associated #0: 10 --> en:leucinosis
    n1=érythermalgie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1539. érythromélalgie --- r_associated #0: 10 --> en:leucinosis
    n1=érythromélalgie | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1540. état de mal épileptique --- r_associated #0: 10 --> en:leucinosis
    n1=état de mal épileptique | n2=en:leucinosis | rel=r_associated | relid=0 | w=10
  1541. Acide aminé --- r_associated #0: 5 --> en:leucinosis
    n1=Acide aminé | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1542. CLN --- r_associated #0: 5 --> en:leucinosis
    n1=CLN | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1543. Maladie génétique --- r_associated #0: 5 --> en:leucinosis
    n1=Maladie génétique | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1544. Maladie rare --- r_associated #0: 5 --> en:leucinosis
    n1=Maladie rare | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1545. Maladies rares --- r_associated #0: 5 --> en:leucinosis
    n1=Maladies rares | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1546. NLCs --- r_associated #0: 5 --> en:leucinosis
    n1=NLCs | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1547. Sirop d'érable --- r_associated #0: 5 --> en:leucinosis
    n1=Sirop d'érable | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1548. abêtalipoprotéinémie --- r_associated #0: 5 --> en:leucinosis
    n1=abêtalipoprotéinémie | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1549. amnésie globale transitoire --- r_associated #0: 5 --> en:leucinosis
    n1=amnésie globale transitoire | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1550. angl. NCLs --- r_associated #0: 5 --> en:leucinosis
    n1=angl. NCLs | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1551. anémie drépanocytaire --- r_associated #0: 5 --> en:leucinosis
    n1=anémie drépanocytaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1552. disomie uniparentale --- r_associated #0: 5 --> en:leucinosis
    n1=disomie uniparentale | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1553. en:Gray platelet syndrome --- r_associated #0: 5 --> en:leucinosis
    n1=en:Gray platelet syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1554. en:Nijmegen breakage syndrome --- r_associated #0: 5 --> en:leucinosis
    n1=en:Nijmegen breakage syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1555. en:Seckel syndrome --- r_associated #0: 5 --> en:leucinosis
    n1=en:Seckel syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1556. en:chromosome --- r_associated #0: 5 --> en:leucinosis
    n1=en:chromosome | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1557. fibrose systémique néphrogénique --- r_associated #0: 5 --> en:leucinosis
    n1=fibrose systémique néphrogénique | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1558. hémochromatose --- r_associated #0: 5 --> en:leucinosis
    n1=hémochromatose | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1559. ichthyose congénitale --- r_associated #0: 5 --> en:leucinosis
    n1=ichthyose congénitale | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1560. maladie de Perthes --- r_associated #0: 5 --> en:leucinosis
    n1=maladie de Perthes | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1561. maladie de Wolman --- r_associated #0: 5 --> en:leucinosis
    n1=maladie de Wolman | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1562. maladie des exostoses multiples --- r_associated #0: 5 --> en:leucinosis
    n1=maladie des exostoses multiples | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1563. myopathie primitive progressive --- r_associated #0: 5 --> en:leucinosis
    n1=myopathie primitive progressive | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1564. neurocysticercose --- r_associated #0: 5 --> en:leucinosis
    n1=neurocysticercose | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1565. ostéochondrodysplasies --- r_associated #0: 5 --> en:leucinosis
    n1=ostéochondrodysplasies | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1566. protéinose alvéolaire pulmonaire --- r_associated #0: 5 --> en:leucinosis
    n1=protéinose alvéolaire pulmonaire | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1567. pseudo-hypoparathyroïdisme --- r_associated #0: 5 --> en:leucinosis
    n1=pseudo-hypoparathyroïdisme | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1568. retardation mentale --- r_associated #0: 5 --> en:leucinosis
    n1=retardation mentale | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1569. sicklanémie --- r_associated #0: 5 --> en:leucinosis
    n1=sicklanémie | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1570. syndrome d'Ehlers-Danlos --- r_associated #0: 5 --> en:leucinosis
    n1=syndrome d'Ehlers-Danlos | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1571. syndrome de Duane --- r_associated #0: 5 --> en:leucinosis
    n1=syndrome de Duane | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1572. syndrome de Jadassohn-Lewandowsky --- r_associated #0: 5 --> en:leucinosis
    n1=syndrome de Jadassohn-Lewandowsky | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1573. syndrome de Stickler --- r_associated #0: 5 --> en:leucinosis
    n1=syndrome de Stickler | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1574. syndrome de Türk-Stilling-Duane --- r_associated #0: 5 --> en:leucinosis
    n1=syndrome de Türk-Stilling-Duane | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1575. syndrome lymphoprolifératif avec autoimmunité --- r_associated #0: 5 --> en:leucinosis
    n1=syndrome lymphoprolifératif avec autoimmunité | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1576. syndrome olfacto-génital --- r_associated #0: 5 --> en:leucinosis
    n1=syndrome olfacto-génital | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
  1577. trouble chromosomique --- r_associated #0: 5 --> en:leucinosis
    n1=trouble chromosomique | n2=en:leucinosis | rel=r_associated | relid=0 | w=5
Le service Rézo permet d'énumérer les relations existant pour un terme. Ce service est interrogeable par programme.
Projet JeuxDeMots - url: http://www.jeuxdemots.org
contact: mathieu.lafourcade@lirmm.fr