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'en:roberts syndrome'
(id=6834166 ; fe=en:roberts syndrome ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=82882.54998779297 creation date=2017-06-25 touchdate=2025-08-14 00:37:32.000)
≈ 1372 relations sortantes

  1. en:roberts syndrome -- r_associated #0: 43 / 1 -> en:acute coronary syndrome
    n1=en:roberts syndrome | n2=en:acute coronary syndrome | rel=r_associated | relid=0 | w=43
  2. en:roberts syndrome -- r_associated #0: 43 / 1 -> en:antiphospholipid syndrome
    n1=en:roberts syndrome | n2=en:antiphospholipid syndrome | rel=r_associated | relid=0 | w=43
  3. en:roberts syndrome -- r_associated #0: 43 / 1 -> en:d-glyceric aciduria
    n1=en:roberts syndrome | n2=en:d-glyceric aciduria | rel=r_associated | relid=0 | w=43
  4. en:roberts syndrome -- r_associated #0: 43 / 1 -> en:erythromelalgia
    n1=en:roberts syndrome | n2=en:erythromelalgia | rel=r_associated | relid=0 | w=43
  5. en:roberts syndrome -- r_associated #0: 43 / 1 -> en:fetal hydantoin syndrome
    n1=en:roberts syndrome | n2=en:fetal hydantoin syndrome | rel=r_associated | relid=0 | w=43
  6. en:roberts syndrome -- r_associated #0: 43 / 1 -> en:hypoplastic left heart syndrome
    n1=en:roberts syndrome | n2=en:hypoplastic left heart syndrome | rel=r_associated | relid=0 | w=43
  7. en:roberts syndrome -- r_associated #0: 43 / 1 -> en:immunoglobulin a deficiency 1
    n1=en:roberts syndrome | n2=en:immunoglobulin a deficiency 1 | rel=r_associated | relid=0 | w=43
  8. en:roberts syndrome -- r_associated #0: 43 / 1 -> en:neuroleptic malignant syndrome
    n1=en:roberts syndrome | n2=en:neuroleptic malignant syndrome | rel=r_associated | relid=0 | w=43
  9. en:roberts syndrome -- r_associated #0: 43 / 1 -> en:penta x syndrome
    n1=en:roberts syndrome | n2=en:penta x syndrome | rel=r_associated | relid=0 | w=43
  10. en:roberts syndrome -- r_associated #0: 43 / 1 -> en:xxyy syndrome
    n1=en:roberts syndrome | n2=en:xxyy syndrome | rel=r_associated | relid=0 | w=43
  11. en:roberts syndrome -- r_associated #0: 43 / 1 -> en:yellow nail syndrome
    n1=en:roberts syndrome | n2=en:yellow nail syndrome | rel=r_associated | relid=0 | w=43
  12. en:roberts syndrome -- r_associated #0: 42 / 0.977 -> en:angelman syndrome
    n1=en:roberts syndrome | n2=en:angelman syndrome | rel=r_associated | relid=0 | w=42
  13. en:roberts syndrome -- r_associated #0: 42 / 0.977 -> en:ehlers-danlos syndrome
    n1=en:roberts syndrome | n2=en:ehlers-danlos syndrome | rel=r_associated | relid=0 | w=42
  14. en:roberts syndrome -- r_associated #0: 42 / 0.977 -> en:fraser syndrome
    n1=en:roberts syndrome | n2=en:fraser syndrome | rel=r_associated | relid=0 | w=42
  15. en:roberts syndrome -- r_associated #0: 42 / 0.977 -> en:nephrocalcinosis
    n1=en:roberts syndrome | n2=en:nephrocalcinosis | rel=r_associated | relid=0 | w=42
  16. en:roberts syndrome -- r_associated #0: 42 / 0.977 -> en:xerophthalmia
    n1=en:roberts syndrome | n2=en:xerophthalmia | rel=r_associated | relid=0 | w=42
  17. en:roberts syndrome -- r_associated #0: 41 / 0.953 -> en:berardinelli-seip congenital lipodystrophy
    n1=en:roberts syndrome | n2=en:berardinelli-seip congenital lipodystrophy | rel=r_associated | relid=0 | w=41
  18. en:roberts syndrome -- r_associated #0: 41 / 0.953 -> en:donohue syndrome
    n1=en:roberts syndrome | n2=en:donohue syndrome | rel=r_associated | relid=0 | w=41
  19. en:roberts syndrome -- r_associated #0: 41 / 0.953 -> en:drug hypersensitivity syndrome
    n1=en:roberts syndrome | n2=en:drug hypersensitivity syndrome | rel=r_associated | relid=0 | w=41
  20. en:roberts syndrome -- r_associated #0: 41 / 0.953 -> en:ellis-van creveld syndrome
    n1=en:roberts syndrome | n2=en:ellis-van creveld syndrome | rel=r_associated | relid=0 | w=41
  21. en:roberts syndrome -- r_associated #0: 41 / 0.953 -> en:fisher syndrome
    n1=en:roberts syndrome | n2=en:fisher syndrome | rel=r_associated | relid=0 | w=41
  22. en:roberts syndrome -- r_associated #0: 41 / 0.953 -> en:meconium plug syndrome
    n1=en:roberts syndrome | n2=en:meconium plug syndrome | rel=r_associated | relid=0 | w=41
  23. en:roberts syndrome -- r_associated #0: 41 / 0.953 -> en:nelson syndrome
    n1=en:roberts syndrome | n2=en:nelson syndrome | rel=r_associated | relid=0 | w=41
  24. en:roberts syndrome -- r_associated #0: 41 / 0.953 -> en:perlman syndrome
    n1=en:roberts syndrome | n2=en:perlman syndrome | rel=r_associated | relid=0 | w=41
  25. en:roberts syndrome -- r_associated #0: 41 / 0.953 -> en:pituitary stalk interruption syndrome
    n1=en:roberts syndrome | n2=en:pituitary stalk interruption syndrome | rel=r_associated | relid=0 | w=41
  26. en:roberts syndrome -- r_associated #0: 41 / 0.953 -> en:synpolydactyly
    n1=en:roberts syndrome | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=41
  27. en:roberts syndrome -- r_associated #0: 41 / 0.953 -> en:whipple disease
    n1=en:roberts syndrome | n2=en:whipple disease | rel=r_associated | relid=0 | w=41
  28. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:alice in wonderland syndrome
    n1=en:roberts syndrome | n2=en:alice in wonderland syndrome | rel=r_associated | relid=0 | w=40
  29. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:carpal tunnel syndrome
    n1=en:roberts syndrome | n2=en:carpal tunnel syndrome | rel=r_associated | relid=0 | w=40
  30. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:congenital central hypoventilation
    n1=en:roberts syndrome | n2=en:congenital central hypoventilation | rel=r_associated | relid=0 | w=40
  31. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:digeorge syndrome
    n1=en:roberts syndrome | n2=en:digeorge syndrome | rel=r_associated | relid=0 | w=40
  32. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:hereditary orotic aciduria
    n1=en:roberts syndrome | n2=en:hereditary orotic aciduria | rel=r_associated | relid=0 | w=40
  33. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:insufficient breast milk syndrome
    n1=en:roberts syndrome | n2=en:insufficient breast milk syndrome | rel=r_associated | relid=0 | w=40
  34. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:pain amplification syndrome
    n1=en:roberts syndrome | n2=en:pain amplification syndrome | rel=r_associated | relid=0 | w=40
  35. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:pelger-huet anomaly
    n1=en:roberts syndrome | n2=en:pelger-huet anomaly | rel=r_associated | relid=0 | w=40
  36. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:perinatal blood aspiration syndrome
    n1=en:roberts syndrome | n2=en:perinatal blood aspiration syndrome | rel=r_associated | relid=0 | w=40
  37. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:pityriasis rubra pilaris
    n1=en:roberts syndrome | n2=en:pityriasis rubra pilaris | rel=r_associated | relid=0 | w=40
  38. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:premenstrual syndrome
    n1=en:roberts syndrome | n2=en:premenstrual syndrome | rel=r_associated | relid=0 | w=40
  39. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:thrombocytopenia 2
    n1=en:roberts syndrome | n2=en:thrombocytopenia 2 | rel=r_associated | relid=0 | w=40
  40. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:triploidy syndrome
    n1=en:roberts syndrome | n2=en:triploidy syndrome | rel=r_associated | relid=0 | w=40
  41. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:wallerian degeneration
    n1=en:roberts syndrome | n2=en:wallerian degeneration | rel=r_associated | relid=0 | w=40
  42. en:roberts syndrome -- r_associated #0: 40 / 0.93 -> en:zellweger syndrome
    n1=en:roberts syndrome | n2=en:zellweger syndrome | rel=r_associated | relid=0 | w=40
  43. en:roberts syndrome -- r_associated #0: 39 / 0.907 -> en:adherence syndrome
    n1=en:roberts syndrome | n2=en:adherence syndrome | rel=r_associated | relid=0 | w=39
  44. en:roberts syndrome -- r_associated #0: 39 / 0.907 -> en:aprosencephaly
    n1=en:roberts syndrome | n2=en:aprosencephaly | rel=r_associated | relid=0 | w=39
  45. en:roberts syndrome -- r_associated #0: 39 / 0.907 -> en:bile acid synthesis defect
    n1=en:roberts syndrome | n2=en:bile acid synthesis defect | rel=r_associated | relid=0 | w=39
  46. en:roberts syndrome -- r_associated #0: 39 / 0.907 -> en:kearns-sayre syndrome
    n1=en:roberts syndrome | n2=en:kearns-sayre syndrome | rel=r_associated | relid=0 | w=39
  47. en:roberts syndrome -- r_associated #0: 39 / 0.907 -> en:lysosomal storage disease
    n1=en:roberts syndrome | n2=en:lysosomal storage disease | rel=r_associated | relid=0 | w=39
  48. en:roberts syndrome -- r_associated #0: 39 / 0.907 -> en:osteopetrosis with renal tubular acidosis
    n1=en:roberts syndrome | n2=en:osteopetrosis with renal tubular acidosis | rel=r_associated | relid=0 | w=39
  49. en:roberts syndrome -- r_associated #0: 39 / 0.907 -> en:very long-chain acyl-coa dehydrogenase deficiency
    n1=en:roberts syndrome | n2=en:very long-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=39
  50. en:roberts syndrome -- r_associated #0: 38 / 0.884 -> en:autoinflammatory syndrome
    n1=en:roberts syndrome | n2=en:autoinflammatory syndrome | rel=r_associated | relid=0 | w=38
  51. en:roberts syndrome -- r_associated #0: 38 / 0.884 -> en:congenital cortical hyperostosis
    n1=en:roberts syndrome | n2=en:congenital cortical hyperostosis | rel=r_associated | relid=0 | w=38
  52. en:roberts syndrome -- r_associated #0: 38 / 0.884 -> en:darier disease
    n1=en:roberts syndrome | n2=en:darier disease | rel=r_associated | relid=0 | w=38
  53. en:roberts syndrome -- r_associated #0: 38 / 0.884 -> en:hyperpipecolatemia
    n1=en:roberts syndrome | n2=en:hyperpipecolatemia | rel=r_associated | relid=0 | w=38
  54. en:roberts syndrome -- r_associated #0: 38 / 0.884 -> en:sunct syndrome
    n1=en:roberts syndrome | n2=en:sunct syndrome | rel=r_associated | relid=0 | w=38
  55. en:roberts syndrome -- r_associated #0: 37 / 0.86 -> en:acrocephalosyndactyly
    n1=en:roberts syndrome | n2=en:acrocephalosyndactyly | rel=r_associated | relid=0 | w=37
  56. en:roberts syndrome -- r_associated #0: 37 / 0.86 -> en:argininosuccinic aciduria
    n1=en:roberts syndrome | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=37
  57. en:roberts syndrome -- r_associated #0: 37 / 0.86 -> en:escobar syndrome
    n1=en:roberts syndrome | n2=en:escobar syndrome | rel=r_associated | relid=0 | w=37
  58. en:roberts syndrome -- r_associated #0: 37 / 0.86 -> en:methylmalonic acidemia
    n1=en:roberts syndrome | n2=en:methylmalonic acidemia | rel=r_associated | relid=0 | w=37
  59. en:roberts syndrome -- r_associated #0: 37 / 0.86 -> en:tempi syndrome
    n1=en:roberts syndrome | n2=en:tempi syndrome | rel=r_associated | relid=0 | w=37
  60. en:roberts syndrome -- r_associated #0: 37 / 0.86 -> en:weill-marchesani syndrome
    n1=en:roberts syndrome | n2=en:weill-marchesani syndrome | rel=r_associated | relid=0 | w=37
  61. en:roberts syndrome -- r_associated #0: 36 / 0.837 -> en:cardiorenal syndrome
    n1=en:roberts syndrome | n2=en:cardiorenal syndrome | rel=r_associated | relid=0 | w=36
  62. en:roberts syndrome -- r_associated #0: 36 / 0.837 -> en:chorea
    n1=en:roberts syndrome | n2=en:chorea | rel=r_associated | relid=0 | w=36
  63. en:roberts syndrome -- r_associated #0: 36 / 0.837 -> en:dravet syndrome
    n1=en:roberts syndrome | n2=en:dravet syndrome | rel=r_associated | relid=0 | w=36
  64. en:roberts syndrome -- r_associated #0: 36 / 0.837 -> en:gastric antral vascular ectasia
    n1=en:roberts syndrome | n2=en:gastric antral vascular ectasia | rel=r_associated | relid=0 | w=36
  65. en:roberts syndrome -- r_associated #0: 36 / 0.837 -> en:heterotaxy syndrome
    n1=en:roberts syndrome | n2=en:heterotaxy syndrome | rel=r_associated | relid=0 | w=36
  66. en:roberts syndrome -- r_associated #0: 36 / 0.837 -> en:mandibuloacral dysplasia with type a lipodystrophy
    n1=en:roberts syndrome | n2=en:mandibuloacral dysplasia with type a lipodystrophy | rel=r_associated | relid=0 | w=36
  67. en:roberts syndrome -- r_associated #0: 36 / 0.837 -> en:neurocysticercosis
    n1=en:roberts syndrome | n2=en:neurocysticercosis | rel=r_associated | relid=0 | w=36
  68. en:roberts syndrome -- r_associated #0: 36 / 0.837 -> en:pallister-hall syndrome
    n1=en:roberts syndrome | n2=en:pallister-hall syndrome | rel=r_associated | relid=0 | w=36
  69. en:roberts syndrome -- r_associated #0: 36 / 0.837 -> en:sunset syndrome
    n1=en:roberts syndrome | n2=en:sunset syndrome | rel=r_associated | relid=0 | w=36
  70. en:roberts syndrome -- r_associated #0: 36 / 0.837 -> en:toxic shock syndrome
    n1=en:roberts syndrome | n2=en:toxic shock syndrome | rel=r_associated | relid=0 | w=36
  71. en:roberts syndrome -- r_associated #0: 36 / 0.837 -> en:usher syndrome
    n1=en:roberts syndrome | n2=en:usher syndrome | rel=r_associated | relid=0 | w=36
  72. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:5' 10' methylenetetrahydrofolate reductase deficiency
    n1=en:roberts syndrome | n2=en:5' 10' methylenetetrahydrofolate reductase deficiency | rel=r_associated | relid=0 | w=35
  73. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:achenbach syndrome
    n1=en:roberts syndrome | n2=en:achenbach syndrome | rel=r_associated | relid=0 | w=35
  74. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:acute intermittent porphyria
    n1=en:roberts syndrome | n2=en:acute intermittent porphyria | rel=r_associated | relid=0 | w=35
  75. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:allgrove syndrome
    n1=en:roberts syndrome | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=35
  76. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:aortic coarctation
    n1=en:roberts syndrome | n2=en:aortic coarctation | rel=r_associated | relid=0 | w=35
  77. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:arnold-chiari malformation
    n1=en:roberts syndrome | n2=en:arnold-chiari malformation | rel=r_associated | relid=0 | w=35
  78. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:basilar artery syndrome
    n1=en:roberts syndrome | n2=en:basilar artery syndrome | rel=r_associated | relid=0 | w=35
  79. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:bonnevie-ullrich syndrome
    n1=en:roberts syndrome | n2=en:bonnevie-ullrich syndrome | rel=r_associated | relid=0 | w=35
  80. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:carbohydrate-deficient glycoprotein syndrome
    n1=en:roberts syndrome | n2=en:carbohydrate-deficient glycoprotein syndrome | rel=r_associated | relid=0 | w=35
  81. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:carnitine palmitoyltransferase i deficiency
    n1=en:roberts syndrome | n2=en:carnitine palmitoyltransferase i deficiency | rel=r_associated | relid=0 | w=35
  82. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:carnitine palmitoyltransferase ii deficiency
    n1=en:roberts syndrome | n2=en:carnitine palmitoyltransferase ii deficiency | rel=r_associated | relid=0 | w=35
  83. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:cauda equina syndrome
    n1=en:roberts syndrome | n2=en:cauda equina syndrome | rel=r_associated | relid=0 | w=35
  84. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:cerebellar mutism
    n1=en:roberts syndrome | n2=en:cerebellar mutism | rel=r_associated | relid=0 | w=35
  85. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:combined lipase deficiency
    n1=en:roberts syndrome | n2=en:combined lipase deficiency | rel=r_associated | relid=0 | w=35
  86. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:congenital disorder of deglycosylation
    n1=en:roberts syndrome | n2=en:congenital disorder of deglycosylation | rel=r_associated | relid=0 | w=35
  87. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:congenital malformation syndrome
    n1=en:roberts syndrome | n2=en:congenital malformation syndrome | rel=r_associated | relid=0 | w=35
  88. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:congenital structural myopathy
    n1=en:roberts syndrome | n2=en:congenital structural myopathy | rel=r_associated | relid=0 | w=35
  89. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:cor triatriatum
    n1=en:roberts syndrome | n2=en:cor triatriatum | rel=r_associated | relid=0 | w=35
  90. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:cryptophthalmos syndrome
    n1=en:roberts syndrome | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=35
  91. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:cystinuria
    n1=en:roberts syndrome | n2=en:cystinuria | rel=r_associated | relid=0 | w=35
  92. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:dentatorubral-pallidoluysian atrophy
    n1=en:roberts syndrome | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=35
  93. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:dialyzer first use syndrome
    n1=en:roberts syndrome | n2=en:dialyzer first use syndrome | rel=r_associated | relid=0 | w=35
  94. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:diencephalic syndrome of infancy
    n1=en:roberts syndrome | n2=en:diencephalic syndrome of infancy | rel=r_associated | relid=0 | w=35
  95. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:erythropoietic porphyria
    n1=en:roberts syndrome | n2=en:erythropoietic porphyria | rel=r_associated | relid=0 | w=35
  96. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:fatal familial insomnia
    n1=en:roberts syndrome | n2=en:fatal familial insomnia | rel=r_associated | relid=0 | w=35
  97. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:fetal akinesia deformation sequence
    n1=en:roberts syndrome | n2=en:fetal akinesia deformation sequence | rel=r_associated | relid=0 | w=35
  98. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:fetal alcohol syndrome
    n1=en:roberts syndrome | n2=en:fetal alcohol syndrome | rel=r_associated | relid=0 | w=35
  99. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:glanzmann thrombasthenia
    n1=en:roberts syndrome | n2=en:glanzmann thrombasthenia | rel=r_associated | relid=0 | w=35
  100. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:griscelli syndrome type 2
    n1=en:roberts syndrome | n2=en:griscelli syndrome type 2 | rel=r_associated | relid=0 | w=35
  101. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:hard skin syndrome parana type
    n1=en:roberts syndrome | n2=en:hard skin syndrome parana type | rel=r_associated | relid=0 | w=35
  102. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:hartnup disease
    n1=en:roberts syndrome | n2=en:hartnup disease | rel=r_associated | relid=0 | w=35
  103. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:hemophagocytic lymphohistiocytosis
    n1=en:roberts syndrome | n2=en:hemophagocytic lymphohistiocytosis | rel=r_associated | relid=0 | w=35
  104. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:holmes-adie syndrome
    n1=en:roberts syndrome | n2=en:holmes-adie syndrome | rel=r_associated | relid=0 | w=35
  105. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:holt-oram syndrome
    n1=en:roberts syndrome | n2=en:holt-oram syndrome | rel=r_associated | relid=0 | w=35
  106. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:hypoalphalipoproteinemia
    n1=en:roberts syndrome | n2=en:hypoalphalipoproteinemia | rel=r_associated | relid=0 | w=35
  107. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:hypohidrotic ectodermal dysplasia with immune deficiency
    n1=en:roberts syndrome | n2=en:hypohidrotic ectodermal dysplasia with immune deficiency | rel=r_associated | relid=0 | w=35
  108. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:immunodeficiency syndrome
    n1=en:roberts syndrome | n2=en:immunodeficiency syndrome | rel=r_associated | relid=0 | w=35
  109. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:immunodeficiency with hyper-igm type 2
    n1=en:roberts syndrome | n2=en:immunodeficiency with hyper-igm type 2 | rel=r_associated | relid=0 | w=35
  110. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:jeune syndrome
    n1=en:roberts syndrome | n2=en:jeune syndrome | rel=r_associated | relid=0 | w=35
  111. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:joubert syndrome
    n1=en:roberts syndrome | n2=en:joubert syndrome | rel=r_associated | relid=0 | w=35
  112. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:lafora disease
    n1=en:roberts syndrome | n2=en:lafora disease | rel=r_associated | relid=0 | w=35
  113. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:lethal multiple pterygium syndrome
    n1=en:roberts syndrome | n2=en:lethal multiple pterygium syndrome | rel=r_associated | relid=0 | w=35
  114. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:levocardia
    n1=en:roberts syndrome | n2=en:levocardia | rel=r_associated | relid=0 | w=35
  115. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:li-fraumeni syndrome
    n1=en:roberts syndrome | n2=en:li-fraumeni syndrome | rel=r_associated | relid=0 | w=35
  116. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:lipase hypersecretion syndrome
    n1=en:roberts syndrome | n2=en:lipase hypersecretion syndrome | rel=r_associated | relid=0 | w=35
  117. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:lipoid proteinosis of urbach and wiethe
    n1=en:roberts syndrome | n2=en:lipoid proteinosis of urbach and wiethe | rel=r_associated | relid=0 | w=35
  118. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:loeys-dietz syndrome
    n1=en:roberts syndrome | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=35
  119. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:loffler syndrome
    n1=en:roberts syndrome | n2=en:loffler syndrome | rel=r_associated | relid=0 | w=35
  120. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:long qt syndrome
    n1=en:roberts syndrome | n2=en:long qt syndrome | rel=r_associated | relid=0 | w=35
  121. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:lubs x-linked mental retardation syndrome
    n1=en:roberts syndrome | n2=en:lubs x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=35
  122. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:lupus anticoagulant disorder
    n1=en:roberts syndrome | n2=en:lupus anticoagulant disorder | rel=r_associated | relid=0 | w=35
  123. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:malabsorption syndrome
    n1=en:roberts syndrome | n2=en:malabsorption syndrome | rel=r_associated | relid=0 | w=35
  124. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:monosomy 13q syndrome
    n1=en:roberts syndrome | n2=en:monosomy 13q syndrome | rel=r_associated | relid=0 | w=35
  125. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:mulibrey nanism
    n1=en:roberts syndrome | n2=en:mulibrey nanism | rel=r_associated | relid=0 | w=35
  126. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:myhre syndrome
    n1=en:roberts syndrome | n2=en:myhre syndrome | rel=r_associated | relid=0 | w=35
  127. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:myokymia
    n1=en:roberts syndrome | n2=en:myokymia | rel=r_associated | relid=0 | w=35
  128. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:nadh dehydrogenase deficiency
    n1=en:roberts syndrome | n2=en:nadh dehydrogenase deficiency | rel=r_associated | relid=0 | w=35
  129. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:neonatal progeroid syndrome
    n1=en:roberts syndrome | n2=en:neonatal progeroid syndrome | rel=r_associated | relid=0 | w=35
  130. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:netherton syndrome
    n1=en:roberts syndrome | n2=en:netherton syndrome | rel=r_associated | relid=0 | w=35
  131. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:neural tube defect
    n1=en:roberts syndrome | n2=en:neural tube defect | rel=r_associated | relid=0 | w=35
  132. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:oculocerebrorenal syndrome
    n1=en:roberts syndrome | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=35
  133. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:pantothenate kinase-associated neurodegeneration
    n1=en:roberts syndrome | n2=en:pantothenate kinase-associated neurodegeneration | rel=r_associated | relid=0 | w=35
  134. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:paraneoplastic syndrome
    n1=en:roberts syndrome | n2=en:paraneoplastic syndrome | rel=r_associated | relid=0 | w=35
  135. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:pearson marrow-pancreas syndrome
    n1=en:roberts syndrome | n2=en:pearson marrow-pancreas syndrome | rel=r_associated | relid=0 | w=35
  136. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:plague
    n1=en:roberts syndrome | n2=en:plague | rel=r_associated | relid=0 | w=35
  137. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:polymyalgia rheumatica
    n1=en:roberts syndrome | n2=en:polymyalgia rheumatica | rel=r_associated | relid=0 | w=35
  138. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:potocki-shaffer syndrome
    n1=en:roberts syndrome | n2=en:potocki-shaffer syndrome | rel=r_associated | relid=0 | w=35
  139. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:prekallikrein deficiency
    n1=en:roberts syndrome | n2=en:prekallikrein deficiency | rel=r_associated | relid=0 | w=35
  140. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:progressive hemifacial atrophy
    n1=en:roberts syndrome | n2=en:progressive hemifacial atrophy | rel=r_associated | relid=0 | w=35
  141. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:pyramidal tract dysfunction
    n1=en:roberts syndrome | n2=en:pyramidal tract dysfunction | rel=r_associated | relid=0 | w=35
  142. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:renal cysts and diabetes syndrome
    n1=en:roberts syndrome | n2=en:renal cysts and diabetes syndrome | rel=r_associated | relid=0 | w=35
  143. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:restless leg syndrome
    n1=en:roberts syndrome | n2=en:restless leg syndrome | rel=r_associated | relid=0 | w=35
  144. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:reversible posterior leukoencephalopathy syndrome
    n1=en:roberts syndrome | n2=en:reversible posterior leukoencephalopathy syndrome | rel=r_associated | relid=0 | w=35
  145. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:reye syndrome
    n1=en:roberts syndrome | n2=en:reye syndrome | rel=r_associated | relid=0 | w=35
  146. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:robinow syndrome
    n1=en:roberts syndrome | n2=en:robinow syndrome | rel=r_associated | relid=0 | w=35
  147. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:sandifer's syndrome
    n1=en:roberts syndrome | n2=en:sandifer's syndrome | rel=r_associated | relid=0 | w=35
  148. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:seckel syndrome
    n1=en:roberts syndrome | n2=en:seckel syndrome | rel=r_associated | relid=0 | w=35
  149. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:sjogren syndrome
    n1=en:roberts syndrome | n2=en:sjogren syndrome | rel=r_associated | relid=0 | w=35
  150. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:spondyloepimetaphyseal dysplasia with joint laxity type 2
    n1=en:roberts syndrome | n2=en:spondyloepimetaphyseal dysplasia with joint laxity type 2 | rel=r_associated | relid=0 | w=35
  151. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:stiff skin syndrome
    n1=en:roberts syndrome | n2=en:stiff skin syndrome | rel=r_associated | relid=0 | w=35
  152. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:sudden infant death syndrome
    n1=en:roberts syndrome | n2=en:sudden infant death syndrome | rel=r_associated | relid=0 | w=35
  153. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:superior vena cava syndrome
    n1=en:roberts syndrome | n2=en:superior vena cava syndrome | rel=r_associated | relid=0 | w=35
  154. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:surfactant protein deficiency
    n1=en:roberts syndrome | n2=en:surfactant protein deficiency | rel=r_associated | relid=0 | w=35
  155. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:systemic inflammatory response syndrome
    n1=en:roberts syndrome | n2=en:systemic inflammatory response syndrome | rel=r_associated | relid=0 | w=35
  156. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:tarsal tunnel syndrome
    n1=en:roberts syndrome | n2=en:tarsal tunnel syndrome | rel=r_associated | relid=0 | w=35
  157. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:togaviridae infection
    n1=en:roberts syndrome | n2=en:togaviridae infection | rel=r_associated | relid=0 | w=35
  158. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:townes-brocks syndrome
    n1=en:roberts syndrome | n2=en:townes-brocks syndrome | rel=r_associated | relid=0 | w=35
  159. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:vitelliform macular dystrophy
    n1=en:roberts syndrome | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=35
  160. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:wandering spleen
    n1=en:roberts syndrome | n2=en:wandering spleen | rel=r_associated | relid=0 | w=35
  161. en:roberts syndrome -- r_associated #0: 35 / 0.814 -> en:xyy syndrome
    n1=en:roberts syndrome | n2=en:xyy syndrome | rel=r_associated | relid=0 | w=35
  162. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:acquired hyperostosis syndrome
    n1=en:roberts syndrome | n2=en:acquired hyperostosis syndrome | rel=r_associated | relid=0 | w=34
  163. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:acrodermatitis
    n1=en:roberts syndrome | n2=en:acrodermatitis | rel=r_associated | relid=0 | w=34
  164. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:acroparesthesia syndrome
    n1=en:roberts syndrome | n2=en:acroparesthesia syndrome | rel=r_associated | relid=0 | w=34
  165. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:alpha-1 antitrypsin deficiency
    n1=en:roberts syndrome | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=34
  166. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:amniotic band syndrome
    n1=en:roberts syndrome | n2=en:amniotic band syndrome | rel=r_associated | relid=0 | w=34
  167. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:aniridia
    n1=en:roberts syndrome | n2=en:aniridia | rel=r_associated | relid=0 | w=34
  168. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:atrophic muscular disorder
    n1=en:roberts syndrome | n2=en:atrophic muscular disorder | rel=r_associated | relid=0 | w=34
  169. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:atypical hemolytic uremic syndrome
    n1=en:roberts syndrome | n2=en:atypical hemolytic uremic syndrome | rel=r_associated | relid=0 | w=34
  170. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:beare-stevenson cutis gyrata syndrome
    n1=en:roberts syndrome | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=34
  171. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:behcet syndrome
    n1=en:roberts syndrome | n2=en:behcet syndrome | rel=r_associated | relid=0 | w=34
  172. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:brain iron accumulation type i syndrome
    n1=en:roberts syndrome | n2=en:brain iron accumulation type i syndrome | rel=r_associated | relid=0 | w=34
  173. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:cadasil syndrome
    n1=en:roberts syndrome | n2=en:cadasil syndrome | rel=r_associated | relid=0 | w=34
  174. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:carnosinemia
    n1=en:roberts syndrome | n2=en:carnosinemia | rel=r_associated | relid=0 | w=34
  175. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:cartilage hair hypoplasia
    n1=en:roberts syndrome | n2=en:cartilage hair hypoplasia | rel=r_associated | relid=0 | w=34
  176. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:cataplexy
    n1=en:roberts syndrome | n2=en:cataplexy | rel=r_associated | relid=0 | w=34
  177. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:central sleep apnea syndrome
    n1=en:roberts syndrome | n2=en:central sleep apnea syndrome | rel=r_associated | relid=0 | w=34
  178. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:choroideremia
    n1=en:roberts syndrome | n2=en:choroideremia | rel=r_associated | relid=0 | w=34
  179. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:churg-strauss syndrome
    n1=en:roberts syndrome | n2=en:churg-strauss syndrome | rel=r_associated | relid=0 | w=34
  180. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:complete trisomy 21 syndrome
    n1=en:roberts syndrome | n2=en:complete trisomy 21 syndrome | rel=r_associated | relid=0 | w=34
  181. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:complex regional pain syndrome i
    n1=en:roberts syndrome | n2=en:complex regional pain syndrome i | rel=r_associated | relid=0 | w=34
  182. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:congenital amegakaryocytic thrombocytopenia
    n1=en:roberts syndrome | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=34
  183. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:dihydropyrimidine dehydrogenase deficiency
    n1=en:roberts syndrome | n2=en:dihydropyrimidine dehydrogenase deficiency | rel=r_associated | relid=0 | w=34
  184. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:duane syndrome
    n1=en:roberts syndrome | n2=en:duane syndrome | rel=r_associated | relid=0 | w=34
  185. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:dubin-johnson syndrome
    n1=en:roberts syndrome | n2=en:dubin-johnson syndrome | rel=r_associated | relid=0 | w=34
  186. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:dyggve-melchior-clausen syndrome
    n1=en:roberts syndrome | n2=en:dyggve-melchior-clausen syndrome | rel=r_associated | relid=0 | w=34
  187. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:dyschromatosis symmetrica hereditaria
    n1=en:roberts syndrome | n2=en:dyschromatosis symmetrica hereditaria | rel=r_associated | relid=0 | w=34
  188. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:encephalocele
    n1=en:roberts syndrome | n2=en:encephalocele | rel=r_associated | relid=0 | w=34
  189. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:endocrine syndrome
    n1=en:roberts syndrome | n2=en:endocrine syndrome | rel=r_associated | relid=0 | w=34
  190. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:familial hypertrophic cardiomyopathy
    n1=en:roberts syndrome | n2=en:familial hypertrophic cardiomyopathy | rel=r_associated | relid=0 | w=34
  191. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:fibrodysplasia ossificans progressiva
    n1=en:roberts syndrome | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=34
  192. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:focal dermal hypoplasia
    n1=en:roberts syndrome | n2=en:focal dermal hypoplasia | rel=r_associated | relid=0 | w=34
  193. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:frontotemporal dementia
    n1=en:roberts syndrome | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=34
  194. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:gangrenous stomatitis
    n1=en:roberts syndrome | n2=en:gangrenous stomatitis | rel=r_associated | relid=0 | w=34
  195. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:glucose-6-phosphate dehydrogenase deficiency
    n1=en:roberts syndrome | n2=en:glucose-6-phosphate dehydrogenase deficiency | rel=r_associated | relid=0 | w=34
  196. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:hantavirus pulmonary syndrome
    n1=en:roberts syndrome | n2=en:hantavirus pulmonary syndrome | rel=r_associated | relid=0 | w=34
  197. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:hellp syndrome
    n1=en:roberts syndrome | n2=en:hellp syndrome | rel=r_associated | relid=0 | w=34
  198. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:hereditary benign intraepithelial dyskeratosis
    n1=en:roberts syndrome | n2=en:hereditary benign intraepithelial dyskeratosis | rel=r_associated | relid=0 | w=34
  199. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:hereditary hyperbilirubinemia
    n1=en:roberts syndrome | n2=en:hereditary hyperbilirubinemia | rel=r_associated | relid=0 | w=34
  200. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:holocarboxylase synthetase deficiency
    n1=en:roberts syndrome | n2=en:holocarboxylase synthetase deficiency | rel=r_associated | relid=0 | w=34
  201. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:hunter syndrome
    n1=en:roberts syndrome | n2=en:hunter syndrome | rel=r_associated | relid=0 | w=34
  202. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:hypereosinophilic syndrome
    n1=en:roberts syndrome | n2=en:hypereosinophilic syndrome | rel=r_associated | relid=0 | w=34
  203. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:hypoplastic right heart syndrome
    n1=en:roberts syndrome | n2=en:hypoplastic right heart syndrome | rel=r_associated | relid=0 | w=34
  204. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:idiopathic cd4-positive t-lymphocytopenia
    n1=en:roberts syndrome | n2=en:idiopathic cd4-positive t-lymphocytopenia | rel=r_associated | relid=0 | w=34
  205. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:infantile neuroaxonal dystrophy
    n1=en:roberts syndrome | n2=en:infantile neuroaxonal dystrophy | rel=r_associated | relid=0 | w=34
  206. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:kartagener syndrome
    n1=en:roberts syndrome | n2=en:kartagener syndrome | rel=r_associated | relid=0 | w=34
  207. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:kluver-bucy syndrome
    n1=en:roberts syndrome | n2=en:kluver-bucy syndrome | rel=r_associated | relid=0 | w=34
  208. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:leptospirosis
    n1=en:roberts syndrome | n2=en:leptospirosis | rel=r_associated | relid=0 | w=34
  209. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:long-chain acyl-coa dehydrogenase deficiency
    n1=en:roberts syndrome | n2=en:long-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=34
  210. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:maple syrup urine disease
    n1=en:roberts syndrome | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=34
  211. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:melorheostosis
    n1=en:roberts syndrome | n2=en:melorheostosis | rel=r_associated | relid=0 | w=34
  212. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:metabolic syndrome
    n1=en:roberts syndrome | n2=en:metabolic syndrome | rel=r_associated | relid=0 | w=34
  213. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:miliaria
    n1=en:roberts syndrome | n2=en:miliaria | rel=r_associated | relid=0 | w=34
  214. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:non-trisomic autosomal aneuploidy
    n1=en:roberts syndrome | n2=en:non-trisomic autosomal aneuploidy | rel=r_associated | relid=0 | w=34
  215. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:orofaciodigital syndrome type 1
    n1=en:roberts syndrome | n2=en:orofaciodigital syndrome type 1 | rel=r_associated | relid=0 | w=34
  216. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:orofaciodigital syndrome type 6
    n1=en:roberts syndrome | n2=en:orofaciodigital syndrome type 6 | rel=r_associated | relid=0 | w=34
  217. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:pachyonychia congenita
    n1=en:roberts syndrome | n2=en:pachyonychia congenita | rel=r_associated | relid=0 | w=34
  218. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:palmar-plantar erythodysthesia
    n1=en:roberts syndrome | n2=en:palmar-plantar erythodysthesia | rel=r_associated | relid=0 | w=34
  219. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:pentalogy of cantrell
    n1=en:roberts syndrome | n2=en:pentalogy of cantrell | rel=r_associated | relid=0 | w=34
  220. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome
    n1=en:roberts syndrome | n2=en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome | rel=r_associated | relid=0 | w=34
  221. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:pick's disease
    n1=en:roberts syndrome | n2=en:pick's disease | rel=r_associated | relid=0 | w=34
  222. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:piebaldism
    n1=en:roberts syndrome | n2=en:piebaldism | rel=r_associated | relid=0 | w=34
  223. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:plummer-vinson syndrome
    n1=en:roberts syndrome | n2=en:plummer-vinson syndrome | rel=r_associated | relid=0 | w=34
  224. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:poland syndrome
    n1=en:roberts syndrome | n2=en:poland syndrome | rel=r_associated | relid=0 | w=34
  225. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:progressive muscular atrophy
    n1=en:roberts syndrome | n2=en:progressive muscular atrophy | rel=r_associated | relid=0 | w=34
  226. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:prune belly syndrome
    n1=en:roberts syndrome | n2=en:prune belly syndrome | rel=r_associated | relid=0 | w=34
  227. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:retinoschisis
    n1=en:roberts syndrome | n2=en:retinoschisis | rel=r_associated | relid=0 | w=34
  228. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:russell-silver syndrome
    n1=en:roberts syndrome | n2=en:russell-silver syndrome | rel=r_associated | relid=0 | w=34
  229. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:sanfilippo syndrome
    n1=en:roberts syndrome | n2=en:sanfilippo syndrome | rel=r_associated | relid=0 | w=34
  230. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:scleromyxedema
    n1=en:roberts syndrome | n2=en:scleromyxedema | rel=r_associated | relid=0 | w=34
  231. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:spinal muscular atrophy
    n1=en:roberts syndrome | n2=en:spinal muscular atrophy | rel=r_associated | relid=0 | w=34
  232. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:subacute sclerosing panencephalitis
    n1=en:roberts syndrome | n2=en:subacute sclerosing panencephalitis | rel=r_associated | relid=0 | w=34
  233. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:thoracic outlet syndrome
    n1=en:roberts syndrome | n2=en:thoracic outlet syndrome | rel=r_associated | relid=0 | w=34
  234. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:torch syndrome
    n1=en:roberts syndrome | n2=en:torch syndrome | rel=r_associated | relid=0 | w=34
  235. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:tracheobronchomegaly
    n1=en:roberts syndrome | n2=en:tracheobronchomegaly | rel=r_associated | relid=0 | w=34
  236. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:weaver syndrome
    n1=en:roberts syndrome | n2=en:weaver syndrome | rel=r_associated | relid=0 | w=34
  237. en:roberts syndrome -- r_associated #0: 34 / 0.791 -> en:wolfram syndrome
    n1=en:roberts syndrome | n2=en:wolfram syndrome | rel=r_associated | relid=0 | w=34
  238. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:aagenaes syndrome
    n1=en:roberts syndrome | n2=en:aagenaes syndrome | rel=r_associated | relid=0 | w=32
  239. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:abstinence syndrome
    n1=en:roberts syndrome | n2=en:abstinence syndrome | rel=r_associated | relid=0 | w=32
  240. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:acquired immunodeficiency syndrome
    n1=en:roberts syndrome | n2=en:acquired immunodeficiency syndrome | rel=r_associated | relid=0 | w=32
  241. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:acute respiratory distress syndrome
    n1=en:roberts syndrome | n2=en:acute respiratory distress syndrome | rel=r_associated | relid=0 | w=32
  242. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:ainhum
    n1=en:roberts syndrome | n2=en:ainhum | rel=r_associated | relid=0 | w=32
  243. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:alkaptonuria
    n1=en:roberts syndrome | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=32
  244. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:bernard-soulier syndrome
    n1=en:roberts syndrome | n2=en:bernard-soulier syndrome | rel=r_associated | relid=0 | w=32
  245. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:campomelic dysplasia
    n1=en:roberts syndrome | n2=en:campomelic dysplasia | rel=r_associated | relid=0 | w=32
  246. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:cardiofaciocutaneous syndrome
    n1=en:roberts syndrome | n2=en:cardiofaciocutaneous syndrome | rel=r_associated | relid=0 | w=32
  247. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:cervicocranial syndrome
    n1=en:roberts syndrome | n2=en:cervicocranial syndrome | rel=r_associated | relid=0 | w=32
  248. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:chromosome 16p11.2 deletion syndrome
    n1=en:roberts syndrome | n2=en:chromosome 16p11.2 deletion syndrome | rel=r_associated | relid=0 | w=32
  249. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:cytokine release syndrome
    n1=en:roberts syndrome | n2=en:cytokine release syndrome | rel=r_associated | relid=0 | w=32
  250. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:d-bifunctional protein deficiency
    n1=en:roberts syndrome | n2=en:d-bifunctional protein deficiency | rel=r_associated | relid=0 | w=32
  251. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:deafness, autosomal recessive 49
    n1=en:roberts syndrome | n2=en:deafness, autosomal recessive 49 | rel=r_associated | relid=0 | w=32
  252. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:deletion 18q syndrome
    n1=en:roberts syndrome | n2=en:deletion 18q syndrome | rel=r_associated | relid=0 | w=32
  253. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:dysfunctional elimination syndrome
    n1=en:roberts syndrome | n2=en:dysfunctional elimination syndrome | rel=r_associated | relid=0 | w=32
  254. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:eisenmenger syndrome
    n1=en:roberts syndrome | n2=en:eisenmenger syndrome | rel=r_associated | relid=0 | w=32
  255. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:episodic pain syndrome, familial, 3
    n1=en:roberts syndrome | n2=en:episodic pain syndrome, familial, 3 | rel=r_associated | relid=0 | w=32
  256. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:erythrokeratodermia variabilis
    n1=en:roberts syndrome | n2=en:erythrokeratodermia variabilis | rel=r_associated | relid=0 | w=32
  257. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:evans syndrome
    n1=en:roberts syndrome | n2=en:evans syndrome | rel=r_associated | relid=0 | w=32
  258. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:frasier syndrome
    n1=en:roberts syndrome | n2=en:frasier syndrome | rel=r_associated | relid=0 | w=32
  259. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:gastroschisis
    n1=en:roberts syndrome | n2=en:gastroschisis | rel=r_associated | relid=0 | w=32
  260. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:gray baby syndrome
    n1=en:roberts syndrome | n2=en:gray baby syndrome | rel=r_associated | relid=0 | w=32
  261. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:greig syndrome
    n1=en:roberts syndrome | n2=en:greig syndrome | rel=r_associated | relid=0 | w=32
  262. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:guillain-barre syndrome
    n1=en:roberts syndrome | n2=en:guillain-barre syndrome | rel=r_associated | relid=0 | w=32
  263. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:hereditary mucosal leukokeratosis
    n1=en:roberts syndrome | n2=en:hereditary mucosal leukokeratosis | rel=r_associated | relid=0 | w=32
  264. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:hereditary persistence of fetal hemoglobin
    n1=en:roberts syndrome | n2=en:hereditary persistence of fetal hemoglobin | rel=r_associated | relid=0 | w=32
  265. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:hermansky-pudlak syndrome
    n1=en:roberts syndrome | n2=en:hermansky-pudlak syndrome | rel=r_associated | relid=0 | w=32
  266. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:hyaline membrane syndrome
    n1=en:roberts syndrome | n2=en:hyaline membrane syndrome | rel=r_associated | relid=0 | w=32
  267. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:hydroa vacciniforme
    n1=en:roberts syndrome | n2=en:hydroa vacciniforme | rel=r_associated | relid=0 | w=32
  268. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:hyperlysinemia
    n1=en:roberts syndrome | n2=en:hyperlysinemia | rel=r_associated | relid=0 | w=32
  269. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
    n1=en:roberts syndrome | n2=en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | rel=r_associated | relid=0 | w=32
  270. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:hyperviscosity syndrome
    n1=en:roberts syndrome | n2=en:hyperviscosity syndrome | rel=r_associated | relid=0 | w=32
  271. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:imperforate vagina
    n1=en:roberts syndrome | n2=en:imperforate vagina | rel=r_associated | relid=0 | w=32
  272. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:iridocorneal endothelial syndrome
    n1=en:roberts syndrome | n2=en:iridocorneal endothelial syndrome | rel=r_associated | relid=0 | w=32
  273. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:juvenile x-linked retinoschisis
    n1=en:roberts syndrome | n2=en:juvenile x-linked retinoschisis | rel=r_associated | relid=0 | w=32
  274. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:kallmann syndrome
    n1=en:roberts syndrome | n2=en:kallmann syndrome | rel=r_associated | relid=0 | w=32
  275. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:leber congenital amaurosis
    n1=en:roberts syndrome | n2=en:leber congenital amaurosis | rel=r_associated | relid=0 | w=32
  276. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:malignant hyperthermia syndrome
    n1=en:roberts syndrome | n2=en:malignant hyperthermia syndrome | rel=r_associated | relid=0 | w=32
  277. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:mansonelliasis
    n1=en:roberts syndrome | n2=en:mansonelliasis | rel=r_associated | relid=0 | w=32
  278. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:maroteaux-lamy syndrome
    n1=en:roberts syndrome | n2=en:maroteaux-lamy syndrome | rel=r_associated | relid=0 | w=32
  279. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:maternal uniparental disomy chromosome 14 syndrome
    n1=en:roberts syndrome | n2=en:maternal uniparental disomy chromosome 14 syndrome | rel=r_associated | relid=0 | w=32
  280. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:melnick-fraser syndrome
    n1=en:roberts syndrome | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=32
  281. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:menkes disease
    n1=en:roberts syndrome | n2=en:menkes disease | rel=r_associated | relid=0 | w=32
  282. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:miller-dieker syndrome
    n1=en:roberts syndrome | n2=en:miller-dieker syndrome | rel=r_associated | relid=0 | w=32
  283. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:norrie syndrome
    n1=en:roberts syndrome | n2=en:norrie syndrome | rel=r_associated | relid=0 | w=32
  284. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:panuveitis
    n1=en:roberts syndrome | n2=en:panuveitis | rel=r_associated | relid=0 | w=32
  285. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:papillon-lefevre syndrome
    n1=en:roberts syndrome | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=32
  286. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:pinta
    n1=en:roberts syndrome | n2=en:pinta | rel=r_associated | relid=0 | w=32
  287. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:popliteal pterygium syndrome
    n1=en:roberts syndrome | n2=en:popliteal pterygium syndrome | rel=r_associated | relid=0 | w=32
  288. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:porphyria cutanea tarda
    n1=en:roberts syndrome | n2=en:porphyria cutanea tarda | rel=r_associated | relid=0 | w=32
  289. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:primary progressive aphasia
    n1=en:roberts syndrome | n2=en:primary progressive aphasia | rel=r_associated | relid=0 | w=32
  290. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:reiter syndrome
    n1=en:roberts syndrome | n2=en:reiter syndrome | rel=r_associated | relid=0 | w=32
  291. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:renal coloboma syndrome
    n1=en:roberts syndrome | n2=en:renal coloboma syndrome | rel=r_associated | relid=0 | w=32
  292. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:rhizomelic dysplasia
    n1=en:roberts syndrome | n2=en:rhizomelic dysplasia | rel=r_associated | relid=0 | w=32
  293. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:sacral agenesis
    n1=en:roberts syndrome | n2=en:sacral agenesis | rel=r_associated | relid=0 | w=32
  294. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:schinzel-giedion midface-retraction syndrome
    n1=en:roberts syndrome | n2=en:schinzel-giedion midface-retraction syndrome | rel=r_associated | relid=0 | w=32
  295. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:scleredema adultorum
    n1=en:roberts syndrome | n2=en:scleredema adultorum | rel=r_associated | relid=0 | w=32
  296. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:short rib-polydactyly syndrome
    n1=en:roberts syndrome | n2=en:short rib-polydactyly syndrome | rel=r_associated | relid=0 | w=32
  297. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:short stature homeobox deficiency
    n1=en:roberts syndrome | n2=en:short stature homeobox deficiency | rel=r_associated | relid=0 | w=32
  298. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:simpson golabi behmel syndrome type 1
    n1=en:roberts syndrome | n2=en:simpson golabi behmel syndrome type 1 | rel=r_associated | relid=0 | w=32
  299. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:smith-lemli-opitz syndrome
    n1=en:roberts syndrome | n2=en:smith-lemli-opitz syndrome | rel=r_associated | relid=0 | w=32
  300. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:staphylococcal scalded skin syndrome
    n1=en:roberts syndrome | n2=en:staphylococcal scalded skin syndrome | rel=r_associated | relid=0 | w=32
  301. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:substance withdrawal syndrome
    n1=en:roberts syndrome | n2=en:substance withdrawal syndrome | rel=r_associated | relid=0 | w=32
  302. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:sudden unexplained infant death
    n1=en:roberts syndrome | n2=en:sudden unexplained infant death | rel=r_associated | relid=0 | w=32
  303. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:swyer james syndrome
    n1=en:roberts syndrome | n2=en:swyer james syndrome | rel=r_associated | relid=0 | w=32
  304. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:teething syndrome
    n1=en:roberts syndrome | n2=en:teething syndrome | rel=r_associated | relid=0 | w=32
  305. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:temporomandibular joint dysfunction syndrome
    n1=en:roberts syndrome | n2=en:temporomandibular joint dysfunction syndrome | rel=r_associated | relid=0 | w=32
  306. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:thalidomide embryopathy syndrome
    n1=en:roberts syndrome | n2=en:thalidomide embryopathy syndrome | rel=r_associated | relid=0 | w=32
  307. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:thyroid dysgenesis
    n1=en:roberts syndrome | n2=en:thyroid dysgenesis | rel=r_associated | relid=0 | w=32
  308. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:thyroid hormone resistance syndrome
    n1=en:roberts syndrome | n2=en:thyroid hormone resistance syndrome | rel=r_associated | relid=0 | w=32
  309. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:tourette syndrome
    n1=en:roberts syndrome | n2=en:tourette syndrome | rel=r_associated | relid=0 | w=32
  310. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:trichorhinophalangeal syndrome type ii
    n1=en:roberts syndrome | n2=en:trichorhinophalangeal syndrome type ii | rel=r_associated | relid=0 | w=32
  311. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:trisomy 14 mosaicism
    n1=en:roberts syndrome | n2=en:trisomy 14 mosaicism | rel=r_associated | relid=0 | w=32
  312. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:turner syndrome
    n1=en:roberts syndrome | n2=en:turner syndrome | rel=r_associated | relid=0 | w=32
  313. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:vacterl association
    n1=en:roberts syndrome | n2=en:vacterl association | rel=r_associated | relid=0 | w=32
  314. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:vascular access steal syndrome
    n1=en:roberts syndrome | n2=en:vascular access steal syndrome | rel=r_associated | relid=0 | w=32
  315. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:wolf-hirschhorn syndrome
    n1=en:roberts syndrome | n2=en:wolf-hirschhorn syndrome | rel=r_associated | relid=0 | w=32
  316. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:x-linked creatine transporter deficiency
    n1=en:roberts syndrome | n2=en:x-linked creatine transporter deficiency | rel=r_associated | relid=0 | w=32
  317. en:roberts syndrome -- r_associated #0: 32 / 0.744 -> en:zollinger ellison syndrome
    n1=en:roberts syndrome | n2=en:zollinger ellison syndrome | rel=r_associated | relid=0 | w=32
  318. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:22q telomere deletion syndrome
    n1=en:roberts syndrome | n2=en:22q telomere deletion syndrome | rel=r_associated | relid=0 | w=31
  319. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:achard syndrome
    n1=en:roberts syndrome | n2=en:achard syndrome | rel=r_associated | relid=0 | w=31
  320. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:adenine phosphoribosyltransferase deficiency
    n1=en:roberts syndrome | n2=en:adenine phosphoribosyltransferase deficiency | rel=r_associated | relid=0 | w=31
  321. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:albinism
    n1=en:roberts syndrome | n2=en:albinism | rel=r_associated | relid=0 | w=31
  322. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:apl differentiation syndrome
    n1=en:roberts syndrome | n2=en:apl differentiation syndrome | rel=r_associated | relid=0 | w=31
  323. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:arrhythmogenic right ventricular dysplasia
    n1=en:roberts syndrome | n2=en:arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=31
  324. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:barrett esophagus
    n1=en:roberts syndrome | n2=en:barrett esophagus | rel=r_associated | relid=0 | w=31
  325. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:bartter syndrome
    n1=en:roberts syndrome | n2=en:bartter syndrome | rel=r_associated | relid=0 | w=31
  326. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:brown-sequard syndrome
    n1=en:roberts syndrome | n2=en:brown-sequard syndrome | rel=r_associated | relid=0 | w=31
  327. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:burning mouth syndrome
    n1=en:roberts syndrome | n2=en:burning mouth syndrome | rel=r_associated | relid=0 | w=31
  328. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:capgras syndrome
    n1=en:roberts syndrome | n2=en:capgras syndrome | rel=r_associated | relid=0 | w=31
  329. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:caroli disease
    n1=en:roberts syndrome | n2=en:caroli disease | rel=r_associated | relid=0 | w=31
  330. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:chronic infantile neurological cutaneous and articular syndrome
    n1=en:roberts syndrome | n2=en:chronic infantile neurological cutaneous and articular syndrome | rel=r_associated | relid=0 | w=31
  331. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:cockayne syndrome
    n1=en:roberts syndrome | n2=en:cockayne syndrome | rel=r_associated | relid=0 | w=31
  332. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:coffin-siris syndrome
    n1=en:roberts syndrome | n2=en:coffin-siris syndrome | rel=r_associated | relid=0 | w=31
  333. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:congenital bilateral aplasia of the vas deferens
    n1=en:roberts syndrome | n2=en:congenital bilateral aplasia of the vas deferens | rel=r_associated | relid=0 | w=31
  334. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:congenital dyserythropoietic anemia
    n1=en:roberts syndrome | n2=en:congenital dyserythropoietic anemia | rel=r_associated | relid=0 | w=31
  335. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:congenital fiber-type disproportion
    n1=en:roberts syndrome | n2=en:congenital fiber-type disproportion | rel=r_associated | relid=0 | w=31
  336. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:cryopyrin-associated periodic syndrome
    n1=en:roberts syndrome | n2=en:cryopyrin-associated periodic syndrome | rel=r_associated | relid=0 | w=31
  337. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:de toni-debre-fanconi syndrome
    n1=en:roberts syndrome | n2=en:de toni-debre-fanconi syndrome | rel=r_associated | relid=0 | w=31
  338. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:deletion 18p syndrome
    n1=en:roberts syndrome | n2=en:deletion 18p syndrome | rel=r_associated | relid=0 | w=31
  339. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:double cortex syndrome
    n1=en:roberts syndrome | n2=en:double cortex syndrome | rel=r_associated | relid=0 | w=31
  340. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:dubowitz syndrome
    n1=en:roberts syndrome | n2=en:dubowitz syndrome | rel=r_associated | relid=0 | w=31
  341. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:empty sella syndrome
    n1=en:roberts syndrome | n2=en:empty sella syndrome | rel=r_associated | relid=0 | w=31
  342. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:familial periodic paralysis
    n1=en:roberts syndrome | n2=en:familial periodic paralysis | rel=r_associated | relid=0 | w=31
  343. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:feingold syndrome
    n1=en:roberts syndrome | n2=en:feingold syndrome | rel=r_associated | relid=0 | w=31
  344. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:genu varum
    n1=en:roberts syndrome | n2=en:genu varum | rel=r_associated | relid=0 | w=31
  345. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:goldenhar syndrome
    n1=en:roberts syndrome | n2=en:goldenhar syndrome | rel=r_associated | relid=0 | w=31
  346. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:hepatolenticular degeneration
    n1=en:roberts syndrome | n2=en:hepatolenticular degeneration | rel=r_associated | relid=0 | w=31
  347. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:hymenolepiasis
    n1=en:roberts syndrome | n2=en:hymenolepiasis | rel=r_associated | relid=0 | w=31
  348. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:intestinal atresia
    n1=en:roberts syndrome | n2=en:intestinal atresia | rel=r_associated | relid=0 | w=31
  349. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:korsakoff syndrome
    n1=en:roberts syndrome | n2=en:korsakoff syndrome | rel=r_associated | relid=0 | w=31
  350. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:lateral medullary syndrome
    n1=en:roberts syndrome | n2=en:lateral medullary syndrome | rel=r_associated | relid=0 | w=31
  351. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:lesch-nyhan syndrome
    n1=en:roberts syndrome | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=31
  352. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:lysinuric protein intolerance
    n1=en:roberts syndrome | n2=en:lysinuric protein intolerance | rel=r_associated | relid=0 | w=31
  353. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:marshall syndrome
    n1=en:roberts syndrome | n2=en:marshall syndrome | rel=r_associated | relid=0 | w=31
  354. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:melkersson-rosenthal syndrome
    n1=en:roberts syndrome | n2=en:melkersson-rosenthal syndrome | rel=r_associated | relid=0 | w=31
  355. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:menopausal syndrome
    n1=en:roberts syndrome | n2=en:menopausal syndrome | rel=r_associated | relid=0 | w=31
  356. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:monilethrix
    n1=en:roberts syndrome | n2=en:monilethrix | rel=r_associated | relid=0 | w=31
  357. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:moyamoya disease
    n1=en:roberts syndrome | n2=en:moyamoya disease | rel=r_associated | relid=0 | w=31
  358. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:mullerian inhibiting factor deficiency
    n1=en:roberts syndrome | n2=en:mullerian inhibiting factor deficiency | rel=r_associated | relid=0 | w=31
  359. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:neuroacanthocytosis
    n1=en:roberts syndrome | n2=en:neuroacanthocytosis | rel=r_associated | relid=0 | w=31
  360. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:obstructive sleep apnea syndrome
    n1=en:roberts syndrome | n2=en:obstructive sleep apnea syndrome | rel=r_associated | relid=0 | w=31
  361. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:oculo-respiratory syndrome
    n1=en:roberts syndrome | n2=en:oculo-respiratory syndrome | rel=r_associated | relid=0 | w=31
  362. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:osteopoikilosis
    n1=en:roberts syndrome | n2=en:osteopoikilosis | rel=r_associated | relid=0 | w=31
  363. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:overlap syndrome
    n1=en:roberts syndrome | n2=en:overlap syndrome | rel=r_associated | relid=0 | w=31
  364. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:pena-shokeir syndrome
    n1=en:roberts syndrome | n2=en:pena-shokeir syndrome | rel=r_associated | relid=0 | w=31
  365. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:pityriasis lichenoides
    n1=en:roberts syndrome | n2=en:pityriasis lichenoides | rel=r_associated | relid=0 | w=31
  366. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:porokeratosis
    n1=en:roberts syndrome | n2=en:porokeratosis | rel=r_associated | relid=0 | w=31
  367. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:progressive bulbar palsy
    n1=en:roberts syndrome | n2=en:progressive bulbar palsy | rel=r_associated | relid=0 | w=31
  368. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:pyruvate dehydrogenase deficiency
    n1=en:roberts syndrome | n2=en:pyruvate dehydrogenase deficiency | rel=r_associated | relid=0 | w=31
  369. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:scheie syndrome
    n1=en:roberts syndrome | n2=en:scheie syndrome | rel=r_associated | relid=0 | w=31
  370. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:short bowel syndrome
    n1=en:roberts syndrome | n2=en:short bowel syndrome | rel=r_associated | relid=0 | w=31
  371. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:sicca syndrome
    n1=en:roberts syndrome | n2=en:sicca syndrome | rel=r_associated | relid=0 | w=31
  372. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:sjogren-larsson syndrome
    n1=en:roberts syndrome | n2=en:sjogren-larsson syndrome | rel=r_associated | relid=0 | w=31
  373. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:stokes-adams syndrome
    n1=en:roberts syndrome | n2=en:stokes-adams syndrome | rel=r_associated | relid=0 | w=31
  374. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:susac syndrome
    n1=en:roberts syndrome | n2=en:susac syndrome | rel=r_associated | relid=0 | w=31
  375. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:syringomyelia
    n1=en:roberts syndrome | n2=en:syringomyelia | rel=r_associated | relid=0 | w=31
  376. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:treacher collins syndrome
    n1=en:roberts syndrome | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=31
  377. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:uveitis glaucoma and hyphema syndrome
    n1=en:roberts syndrome | n2=en:uveitis glaucoma and hyphema syndrome | rel=r_associated | relid=0 | w=31
  378. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:west syndrome
    n1=en:roberts syndrome | n2=en:west syndrome | rel=r_associated | relid=0 | w=31
  379. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:xxxy and xxxxy syndrome
    n1=en:roberts syndrome | n2=en:xxxy and xxxxy syndrome | rel=r_associated | relid=0 | w=31
  380. en:roberts syndrome -- r_associated #0: 31 / 0.721 -> en:xxxy syndrome
    n1=en:roberts syndrome | n2=en:xxxy syndrome | rel=r_associated | relid=0 | w=31
  381. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:andersen syndrome
    n1=en:roberts syndrome | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=30
  382. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:anencephaly
    n1=en:roberts syndrome | n2=en:anencephaly | rel=r_associated | relid=0 | w=30
  383. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:arakawa syndrome ii
    n1=en:roberts syndrome | n2=en:arakawa syndrome ii | rel=r_associated | relid=0 | w=30
  384. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:atransferrinemia
    n1=en:roberts syndrome | n2=en:atransferrinemia | rel=r_associated | relid=0 | w=30
  385. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:benign mucous membrane pemphigoid
    n1=en:roberts syndrome | n2=en:benign mucous membrane pemphigoid | rel=r_associated | relid=0 | w=30
  386. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:biotinidase deficiency
    n1=en:roberts syndrome | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=30
  387. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:cerebrotendinous xanthomatosis
    n1=en:roberts syndrome | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=30
  388. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:chondrodysplasia punctata
    n1=en:roberts syndrome | n2=en:chondrodysplasia punctata | rel=r_associated | relid=0 | w=30
  389. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:chronic fatigue syndrome
    n1=en:roberts syndrome | n2=en:chronic fatigue syndrome | rel=r_associated | relid=0 | w=30
  390. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:congenital myasthenic syndrome
    n1=en:roberts syndrome | n2=en:congenital myasthenic syndrome | rel=r_associated | relid=0 | w=30
  391. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:congenital varicella syndrome
    n1=en:roberts syndrome | n2=en:congenital varicella syndrome | rel=r_associated | relid=0 | w=30
  392. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:conn syndrome
    n1=en:roberts syndrome | n2=en:conn syndrome | rel=r_associated | relid=0 | w=30
  393. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:deafness, autosomal recessive 28
    n1=en:roberts syndrome | n2=en:deafness, autosomal recessive 28 | rel=r_associated | relid=0 | w=30
  394. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:dentinogenesis imperfecta
    n1=en:roberts syndrome | n2=en:dentinogenesis imperfecta | rel=r_associated | relid=0 | w=30
  395. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:diarrhea-associated hemolytic uremic syndrome
    n1=en:roberts syndrome | n2=en:diarrhea-associated hemolytic uremic syndrome | rel=r_associated | relid=0 | w=30
  396. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:dry eye syndrome
    n1=en:roberts syndrome | n2=en:dry eye syndrome | rel=r_associated | relid=0 | w=30
  397. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:dysequilibrium syndrome
    n1=en:roberts syndrome | n2=en:dysequilibrium syndrome | rel=r_associated | relid=0 | w=30
  398. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:ectrodactyly
    n1=en:roberts syndrome | n2=en:ectrodactyly | rel=r_associated | relid=0 | w=30
  399. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:epidermolysis bullosa
    n1=en:roberts syndrome | n2=en:epidermolysis bullosa | rel=r_associated | relid=0 | w=30
  400. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:familial dysautonomia
    n1=en:roberts syndrome | n2=en:familial dysautonomia | rel=r_associated | relid=0 | w=30
  401. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:familial partial lipodystrophy
    n1=en:roberts syndrome | n2=en:familial partial lipodystrophy | rel=r_associated | relid=0 | w=30
  402. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:fanconi syndrome
    n1=en:roberts syndrome | n2=en:fanconi syndrome | rel=r_associated | relid=0 | w=30
  403. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:fetal valproate syndrome
    n1=en:roberts syndrome | n2=en:fetal valproate syndrome | rel=r_associated | relid=0 | w=30
  404. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:fryns syndrome
    n1=en:roberts syndrome | n2=en:fryns syndrome | rel=r_associated | relid=0 | w=30
  405. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:gasping syndrome
    n1=en:roberts syndrome | n2=en:gasping syndrome | rel=r_associated | relid=0 | w=30
  406. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:glycine encephalopathy
    n1=en:roberts syndrome | n2=en:glycine encephalopathy | rel=r_associated | relid=0 | w=30
  407. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:hair tourniquet
    n1=en:roberts syndrome | n2=en:hair tourniquet | rel=r_associated | relid=0 | w=30
  408. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:heterotaxy syndrome with asplenia
    n1=en:roberts syndrome | n2=en:heterotaxy syndrome with asplenia | rel=r_associated | relid=0 | w=30
  409. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:high molecular weight kininogen deficiency
    n1=en:roberts syndrome | n2=en:high molecular weight kininogen deficiency | rel=r_associated | relid=0 | w=30
  410. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:homocystinuria
    n1=en:roberts syndrome | n2=en:homocystinuria | rel=r_associated | relid=0 | w=30
  411. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:hurler syndrome
    n1=en:roberts syndrome | n2=en:hurler syndrome | rel=r_associated | relid=0 | w=30
  412. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:idiopathic hypersomnolence
    n1=en:roberts syndrome | n2=en:idiopathic hypersomnolence | rel=r_associated | relid=0 | w=30
  413. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:imperforate anus
    n1=en:roberts syndrome | n2=en:imperforate anus | rel=r_associated | relid=0 | w=30
  414. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:incontinentia pigmenti
    n1=en:roberts syndrome | n2=en:incontinentia pigmenti | rel=r_associated | relid=0 | w=30
  415. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:kabuki syndrome
    n1=en:roberts syndrome | n2=en:kabuki syndrome | rel=r_associated | relid=0 | w=30
  416. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:kawasaki disease
    n1=en:roberts syndrome | n2=en:kawasaki disease | rel=r_associated | relid=0 | w=30
  417. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:kernicterus
    n1=en:roberts syndrome | n2=en:kernicterus | rel=r_associated | relid=0 | w=30
  418. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:laurence-moon syndrome
    n1=en:roberts syndrome | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=30
  419. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:malformations of cortical development
    n1=en:roberts syndrome | n2=en:malformations of cortical development | rel=r_associated | relid=0 | w=30
  420. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:marburg virus disease
    n1=en:roberts syndrome | n2=en:marburg virus disease | rel=r_associated | relid=0 | w=30
  421. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:methionine adenosyltransferase deficiency
    n1=en:roberts syndrome | n2=en:methionine adenosyltransferase deficiency | rel=r_associated | relid=0 | w=30
  422. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:mitochondrial trifunctional protein deficiency
    n1=en:roberts syndrome | n2=en:mitochondrial trifunctional protein deficiency | rel=r_associated | relid=0 | w=30
  423. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:molybdenum cofactor deficiency
    n1=en:roberts syndrome | n2=en:molybdenum cofactor deficiency | rel=r_associated | relid=0 | w=30
  424. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:muenke syndrome
    n1=en:roberts syndrome | n2=en:muenke syndrome | rel=r_associated | relid=0 | w=30
  425. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:multiple system atrophy
    n1=en:roberts syndrome | n2=en:multiple system atrophy | rel=r_associated | relid=0 | w=30
  426. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:muscular dystrophy
    n1=en:roberts syndrome | n2=en:muscular dystrophy | rel=r_associated | relid=0 | w=30
  427. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:n-acetylglutamate synthase deficiency
    n1=en:roberts syndrome | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=30
  428. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:neuromyelitis optica
    n1=en:roberts syndrome | n2=en:neuromyelitis optica | rel=r_associated | relid=0 | w=30
  429. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:organic brain syndrome
    n1=en:roberts syndrome | n2=en:organic brain syndrome | rel=r_associated | relid=0 | w=30
  430. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:ossification of posterior longitudinal ligament
    n1=en:roberts syndrome | n2=en:ossification of posterior longitudinal ligament | rel=r_associated | relid=0 | w=30
  431. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:overgrowth syndrome
    n1=en:roberts syndrome | n2=en:overgrowth syndrome | rel=r_associated | relid=0 | w=30
  432. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:perthes disease
    n1=en:roberts syndrome | n2=en:perthes disease | rel=r_associated | relid=0 | w=30
  433. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:pettigrew syndrome
    n1=en:roberts syndrome | n2=en:pettigrew syndrome | rel=r_associated | relid=0 | w=30
  434. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:pierre robin syndrome
    n1=en:roberts syndrome | n2=en:pierre robin syndrome | rel=r_associated | relid=0 | w=30
  435. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:poems syndrome
    n1=en:roberts syndrome | n2=en:poems syndrome | rel=r_associated | relid=0 | w=30
  436. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:post-pericardiotomy syndrome
    n1=en:roberts syndrome | n2=en:post-pericardiotomy syndrome | rel=r_associated | relid=0 | w=30
  437. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:primary fanconi syndrome
    n1=en:roberts syndrome | n2=en:primary fanconi syndrome | rel=r_associated | relid=0 | w=30
  438. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:progeria
    n1=en:roberts syndrome | n2=en:progeria | rel=r_associated | relid=0 | w=30
  439. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:prolidase deficiency
    n1=en:roberts syndrome | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=30
  440. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:rieger syndrome type 1
    n1=en:roberts syndrome | n2=en:rieger syndrome type 1 | rel=r_associated | relid=0 | w=30
  441. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:shprintzen-goldberg craniosynostosis syndrome
    n1=en:roberts syndrome | n2=en:shprintzen-goldberg craniosynostosis syndrome | rel=r_associated | relid=0 | w=30
  442. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:spasmodic torticollis
    n1=en:roberts syndrome | n2=en:spasmodic torticollis | rel=r_associated | relid=0 | w=30
  443. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:stickler syndrome
    n1=en:roberts syndrome | n2=en:stickler syndrome | rel=r_associated | relid=0 | w=30
  444. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:tangier disease
    n1=en:roberts syndrome | n2=en:tangier disease | rel=r_associated | relid=0 | w=30
  445. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:tooth and nail syndrome
    n1=en:roberts syndrome | n2=en:tooth and nail syndrome | rel=r_associated | relid=0 | w=30
  446. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:transposition of great vessels
    n1=en:roberts syndrome | n2=en:transposition of great vessels | rel=r_associated | relid=0 | w=30
  447. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:trichothiodystrophy
    n1=en:roberts syndrome | n2=en:trichothiodystrophy | rel=r_associated | relid=0 | w=30
  448. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:uniparental disomy
    n1=en:roberts syndrome | n2=en:uniparental disomy | rel=r_associated | relid=0 | w=30
  449. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:von hippel-lindau syndrome
    n1=en:roberts syndrome | n2=en:von hippel-lindau syndrome | rel=r_associated | relid=0 | w=30
  450. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:waterhouse-friderichsen syndrome
    n1=en:roberts syndrome | n2=en:waterhouse-friderichsen syndrome | rel=r_associated | relid=0 | w=30
  451. en:roberts syndrome -- r_associated #0: 30 / 0.698 -> en:x-linked dominant hypophosphatemic rickets
    n1=en:roberts syndrome | n2=en:x-linked dominant hypophosphatemic rickets | rel=r_associated | relid=0 | w=30
  452. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:17q21 microdeletion syndrome
    n1=en:roberts syndrome | n2=en:17q21 microdeletion syndrome | rel=r_associated | relid=0 | w=29
  453. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:achondrogenesis
    n1=en:roberts syndrome | n2=en:achondrogenesis | rel=r_associated | relid=0 | w=29
  454. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:achromatopsia
    n1=en:roberts syndrome | n2=en:achromatopsia | rel=r_associated | relid=0 | w=29
  455. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:acromegaly
    n1=en:roberts syndrome | n2=en:acromegaly | rel=r_associated | relid=0 | w=29
  456. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:agnosia
    n1=en:roberts syndrome | n2=en:agnosia | rel=r_associated | relid=0 | w=29
  457. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:alagille syndrome
    n1=en:roberts syndrome | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=29
  458. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:albright's hereditary osteodystrophy
    n1=en:roberts syndrome | n2=en:albright's hereditary osteodystrophy | rel=r_associated | relid=0 | w=29
  459. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:allan-herndon-dudley syndrome
    n1=en:roberts syndrome | n2=en:allan-herndon-dudley syndrome | rel=r_associated | relid=0 | w=29
  460. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:analbuminemia
    n1=en:roberts syndrome | n2=en:analbuminemia | rel=r_associated | relid=0 | w=29
  461. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:antithrombin iii deficiency
    n1=en:roberts syndrome | n2=en:antithrombin iii deficiency | rel=r_associated | relid=0 | w=29
  462. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:argininemia
    n1=en:roberts syndrome | n2=en:argininemia | rel=r_associated | relid=0 | w=29
  463. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal recessive hypohidrotic ectodermal dysplasia
    n1=en:roberts syndrome | n2=en:autosomal recessive hypohidrotic ectodermal dysplasia | rel=r_associated | relid=0 | w=29
  464. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:barth syndrome
    n1=en:roberts syndrome | n2=en:barth syndrome | rel=r_associated | relid=0 | w=29
  465. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:cleidocranial dysplasia
    n1=en:roberts syndrome | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=29
  466. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:codas syndrome
    n1=en:roberts syndrome | n2=en:codas syndrome | rel=r_associated | relid=0 | w=29
  467. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:compartment syndrome
    n1=en:roberts syndrome | n2=en:compartment syndrome | rel=r_associated | relid=0 | w=29
  468. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:complete trisomy 18 syndrome
    n1=en:roberts syndrome | n2=en:complete trisomy 18 syndrome | rel=r_associated | relid=0 | w=29
  469. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:congenital pain insensitivity
    n1=en:roberts syndrome | n2=en:congenital pain insensitivity | rel=r_associated | relid=0 | w=29
  470. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:cri du chat syndrome
    n1=en:roberts syndrome | n2=en:cri du chat syndrome | rel=r_associated | relid=0 | w=29
  471. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:diffuse cerebral sclerosis of schilder
    n1=en:roberts syndrome | n2=en:diffuse cerebral sclerosis of schilder | rel=r_associated | relid=0 | w=29
  472. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:dumping syndrome
    n1=en:roberts syndrome | n2=en:dumping syndrome | rel=r_associated | relid=0 | w=29
  473. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:ebstein anomaly
    n1=en:roberts syndrome | n2=en:ebstein anomaly | rel=r_associated | relid=0 | w=29
  474. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:esco2 gene
    n1=en:roberts syndrome | n2=en:esco2 gene | rel=r_associated | relid=0 | w=29
  475. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:familial mediterranean fever
    n1=en:roberts syndrome | n2=en:familial mediterranean fever | rel=r_associated | relid=0 | w=29
  476. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:farber lipogranulomatosis
    n1=en:roberts syndrome | n2=en:farber lipogranulomatosis | rel=r_associated | relid=0 | w=29
  477. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:fox-fordyce disease
    n1=en:roberts syndrome | n2=en:fox-fordyce disease | rel=r_associated | relid=0 | w=29
  478. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:fragile x syndrome
    n1=en:roberts syndrome | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=29
  479. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:generalized arterial calcification of infancy 1
    n1=en:roberts syndrome | n2=en:generalized arterial calcification of infancy 1 | rel=r_associated | relid=0 | w=29
  480. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:gitelman syndrome
    n1=en:roberts syndrome | n2=en:gitelman syndrome | rel=r_associated | relid=0 | w=29
  481. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:goodpasture syndrome
    n1=en:roberts syndrome | n2=en:goodpasture syndrome | rel=r_associated | relid=0 | w=29
  482. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:hajdu-cheney syndrome
    n1=en:roberts syndrome | n2=en:hajdu-cheney syndrome | rel=r_associated | relid=0 | w=29
  483. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:hepatorenal syndrome
    n1=en:roberts syndrome | n2=en:hepatorenal syndrome | rel=r_associated | relid=0 | w=29
  484. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:hereditary coproporphyria
    n1=en:roberts syndrome | n2=en:hereditary coproporphyria | rel=r_associated | relid=0 | w=29
  485. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:hereditary fructose intolerance
    n1=en:roberts syndrome | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=29
  486. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:hypokalemic periodic paralysis
    n1=en:roberts syndrome | n2=en:hypokalemic periodic paralysis | rel=r_associated | relid=0 | w=29
  487. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:infantile convulsions and paroxysmal choreoathetosis, familial
    n1=en:roberts syndrome | n2=en:infantile convulsions and paroxysmal choreoathetosis, familial | rel=r_associated | relid=0 | w=29
  488. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:kimura disease
    n1=en:roberts syndrome | n2=en:kimura disease | rel=r_associated | relid=0 | w=29
  489. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:klippel-feil syndrome
    n1=en:roberts syndrome | n2=en:klippel-feil syndrome | rel=r_associated | relid=0 | w=29
  490. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:leber hereditary optic atrophy
    n1=en:roberts syndrome | n2=en:leber hereditary optic atrophy | rel=r_associated | relid=0 | w=29
  491. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:leri-weill dyschondrosteosis
    n1=en:roberts syndrome | n2=en:leri-weill dyschondrosteosis | rel=r_associated | relid=0 | w=29
  492. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:leriche syndrome
    n1=en:roberts syndrome | n2=en:leriche syndrome | rel=r_associated | relid=0 | w=29
  493. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:lymphedema-distichiasis syndrome
    n1=en:roberts syndrome | n2=en:lymphedema-distichiasis syndrome | rel=r_associated | relid=0 | w=29
  494. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:mallory-weiss syndrome
    n1=en:roberts syndrome | n2=en:mallory-weiss syndrome | rel=r_associated | relid=0 | w=29
  495. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:marfan syndrome
    n1=en:roberts syndrome | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=29
  496. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:meesmann corneal dystrophy
    n1=en:roberts syndrome | n2=en:meesmann corneal dystrophy | rel=r_associated | relid=0 | w=29
  497. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:merrf syndrome
    n1=en:roberts syndrome | n2=en:merrf syndrome | rel=r_associated | relid=0 | w=29
  498. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:mevalonate kinase deficiency
    n1=en:roberts syndrome | n2=en:mevalonate kinase deficiency | rel=r_associated | relid=0 | w=29
  499. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:multicentric osteolysis, nodulosis, and arthropathy
    n1=en:roberts syndrome | n2=en:multicentric osteolysis, nodulosis, and arthropathy | rel=r_associated | relid=0 | w=29
  500. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:myositis
    n1=en:roberts syndrome | n2=en:myositis | rel=r_associated | relid=0 | w=29
  501. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:neuronal intranuclear inclusion disease
    n1=en:roberts syndrome | n2=en:neuronal intranuclear inclusion disease | rel=r_associated | relid=0 | w=29
  502. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:noonan syndrome
    n1=en:roberts syndrome | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=29
  503. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:oeis complex
    n1=en:roberts syndrome | n2=en:oeis complex | rel=r_associated | relid=0 | w=29
  504. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:optic neuritis
    n1=en:roberts syndrome | n2=en:optic neuritis | rel=r_associated | relid=0 | w=29
  505. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:pain agnosia
    n1=en:roberts syndrome | n2=en:pain agnosia | rel=r_associated | relid=0 | w=29
  506. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:paroxysmal extreme pain disorder
    n1=en:roberts syndrome | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=29
  507. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:postural orthostatic tachycardia syndrome
    n1=en:roberts syndrome | n2=en:postural orthostatic tachycardia syndrome | rel=r_associated | relid=0 | w=29
  508. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:prader-willi syndrome
    n1=en:roberts syndrome | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=29
  509. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:progressive supranuclear palsy
    n1=en:roberts syndrome | n2=en:progressive supranuclear palsy | rel=r_associated | relid=0 | w=29
  510. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:prosopagnosia
    n1=en:roberts syndrome | n2=en:prosopagnosia | rel=r_associated | relid=0 | w=29
  511. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:pseudotrisomy 13 syndrome
    n1=en:roberts syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  512. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:red man syndrome
    n1=en:roberts syndrome | n2=en:red man syndrome | rel=r_associated | relid=0 | w=29
  513. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:smith-magenis syndrome
    n1=en:roberts syndrome | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=29
  514. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:stargardt disease
    n1=en:roberts syndrome | n2=en:stargardt disease | rel=r_associated | relid=0 | w=29
  515. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:status epilepticus
    n1=en:roberts syndrome | n2=en:status epilepticus | rel=r_associated | relid=0 | w=29
  516. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:takotsubo cardiomyopathy
    n1=en:roberts syndrome | n2=en:takotsubo cardiomyopathy | rel=r_associated | relid=0 | w=29
  517. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:tolosa-hunt syndrome
    n1=en:roberts syndrome | n2=en:tolosa-hunt syndrome | rel=r_associated | relid=0 | w=29
  518. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:trichinosis
    n1=en:roberts syndrome | n2=en:trichinosis | rel=r_associated | relid=0 | w=29
  519. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:trichorhinophalangeal syndrome type i
    n1=en:roberts syndrome | n2=en:trichorhinophalangeal syndrome type i | rel=r_associated | relid=0 | w=29
  520. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:van der woude syndrome
    n1=en:roberts syndrome | n2=en:van der woude syndrome | rel=r_associated | relid=0 | w=29
  521. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:variegate porphyria
    n1=en:roberts syndrome | n2=en:variegate porphyria | rel=r_associated | relid=0 | w=29
  522. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> en:werner syndrome
    n1=en:roberts syndrome | n2=en:werner syndrome | rel=r_associated | relid=0 | w=29
  523. en:roberts syndrome -- r_associated #0: 29 / 0.674 -> paralysies périodiques familiales
    n1=en:roberts syndrome | n2=paralysies périodiques familiales | rel=r_associated | relid=0 | w=29
  524. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:abetalipoproteinemia
    n1=en:roberts syndrome | n2=en:abetalipoproteinemia | rel=r_associated | relid=0 | w=28
  525. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:acatalasemia
    n1=en:roberts syndrome | n2=en:acatalasemia | rel=r_associated | relid=0 | w=28
  526. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:adiposis dolorosa
    n1=en:roberts syndrome | n2=en:adiposis dolorosa | rel=r_associated | relid=0 | w=28
  527. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:alstrom syndrome
    n1=en:roberts syndrome | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=28
  528. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:amaurosis fugax
    n1=en:roberts syndrome | n2=en:amaurosis fugax | rel=r_associated | relid=0 | w=28
  529. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:anhidrotic ectodermal dysplasia 1
    n1=en:roberts syndrome | n2=en:anhidrotic ectodermal dysplasia 1 | rel=r_associated | relid=0 | w=28
  530. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:aortic arch syndrome
    n1=en:roberts syndrome | n2=en:aortic arch syndrome | rel=r_associated | relid=0 | w=28
  531. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:arthrogryposis
    n1=en:roberts syndrome | n2=en:arthrogryposis | rel=r_associated | relid=0 | w=28
  532. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:bardet-biedl syndrome
    n1=en:roberts syndrome | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=28
  533. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:blau syndrome
    n1=en:roberts syndrome | n2=en:blau syndrome | rel=r_associated | relid=0 | w=28
  534. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:calciphylaxis
    n1=en:roberts syndrome | n2=en:calciphylaxis | rel=r_associated | relid=0 | w=28
  535. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:capillary leak syndrome
    n1=en:roberts syndrome | n2=en:capillary leak syndrome | rel=r_associated | relid=0 | w=28
  536. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:charge syndrome
    n1=en:roberts syndrome | n2=en:charge syndrome | rel=r_associated | relid=0 | w=28
  537. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:chilblains
    n1=en:roberts syndrome | n2=en:chilblains | rel=r_associated | relid=0 | w=28
  538. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:chromosome 2q37 deletion syndrome
    n1=en:roberts syndrome | n2=en:chromosome 2q37 deletion syndrome | rel=r_associated | relid=0 | w=28
  539. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:complete trisomy 13 syndrome
    n1=en:roberts syndrome | n2=en:complete trisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  540. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:congenital insensitivity to pain with anhidrosis
    n1=en:roberts syndrome | n2=en:congenital insensitivity to pain with anhidrosis | rel=r_associated | relid=0 | w=28
  541. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:crest syndrome
    n1=en:roberts syndrome | n2=en:crest syndrome | rel=r_associated | relid=0 | w=28
  542. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:cytochrome-c oxidase deficiency
    n1=en:roberts syndrome | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=28
  543. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:down syndrome
    n1=en:roberts syndrome | n2=en:down syndrome | rel=r_associated | relid=0 | w=28
  544. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:drug- and toxin-induced pulmonary arterial hypertension
    n1=en:roberts syndrome | n2=en:drug- and toxin-induced pulmonary arterial hypertension | rel=r_associated | relid=0 | w=28
  545. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:erythropoietic protoporphyria
    n1=en:roberts syndrome | n2=en:erythropoietic protoporphyria | rel=r_associated | relid=0 | w=28
  546. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:exfoliation syndrome
    n1=en:roberts syndrome | n2=en:exfoliation syndrome | rel=r_associated | relid=0 | w=28
  547. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:factor v leiden
    n1=en:roberts syndrome | n2=en:factor v leiden | rel=r_associated | relid=0 | w=28
  548. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:familial atypical hemolytic uremic syndrome
    n1=en:roberts syndrome | n2=en:familial atypical hemolytic uremic syndrome | rel=r_associated | relid=0 | w=28
  549. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:familial juvenile nephronophthisis
    n1=en:roberts syndrome | n2=en:familial juvenile nephronophthisis | rel=r_associated | relid=0 | w=28
  550. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:fetal retinoid syndrome
    n1=en:roberts syndrome | n2=en:fetal retinoid syndrome | rel=r_associated | relid=0 | w=28
  551. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:fetal warfarin syndrome
    n1=en:roberts syndrome | n2=en:fetal warfarin syndrome | rel=r_associated | relid=0 | w=28
  552. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:fragile x tremor/ataxia syndrome
    n1=en:roberts syndrome | n2=en:fragile x tremor/ataxia syndrome | rel=r_associated | relid=0 | w=28
  553. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:gerstmann-straussler-scheinker disease
    n1=en:roberts syndrome | n2=en:gerstmann-straussler-scheinker disease | rel=r_associated | relid=0 | w=28
  554. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:giant axonal neuropathy
    n1=en:roberts syndrome | n2=en:giant axonal neuropathy | rel=r_associated | relid=0 | w=28
  555. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:glycogen storage disease
    n1=en:roberts syndrome | n2=en:glycogen storage disease | rel=r_associated | relid=0 | w=28
  556. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:gyrate atrophy
    n1=en:roberts syndrome | n2=en:gyrate atrophy | rel=r_associated | relid=0 | w=28
  557. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:hallermann syndrome
    n1=en:roberts syndrome | n2=en:hallermann syndrome | rel=r_associated | relid=0 | w=28
  558. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:hemorrhagic fever with renal syndrome
    n1=en:roberts syndrome | n2=en:hemorrhagic fever with renal syndrome | rel=r_associated | relid=0 | w=28
  559. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:hereditary angioedema
    n1=en:roberts syndrome | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=28
  560. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:heritable pulmonary arterial hypertension
    n1=en:roberts syndrome | n2=en:heritable pulmonary arterial hypertension | rel=r_associated | relid=0 | w=28
  561. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:heterotaxy syndrome with polysplenia
    n1=en:roberts syndrome | n2=en:heterotaxy syndrome with polysplenia | rel=r_associated | relid=0 | w=28
  562. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:hydrops fetalis
    n1=en:roberts syndrome | n2=en:hydrops fetalis | rel=r_associated | relid=0 | w=28
  563. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:hyperglycerolemia
    n1=en:roberts syndrome | n2=en:hyperglycerolemia | rel=r_associated | relid=0 | w=28
  564. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:hypophosphatasia
    n1=en:roberts syndrome | n2=en:hypophosphatasia | rel=r_associated | relid=0 | w=28
  565. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:inspissated bile syndrome
    n1=en:roberts syndrome | n2=en:inspissated bile syndrome | rel=r_associated | relid=0 | w=28
  566. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:jackson-weiss syndrome
    n1=en:roberts syndrome | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=28
  567. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:jacobsen syndrome
    n1=en:roberts syndrome | n2=en:jacobsen syndrome | rel=r_associated | relid=0 | w=28
  568. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:jervell and lange nielsen syndrome
    n1=en:roberts syndrome | n2=en:jervell and lange nielsen syndrome | rel=r_associated | relid=0 | w=28
  569. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:klinefelter syndrome
    n1=en:roberts syndrome | n2=en:klinefelter syndrome | rel=r_associated | relid=0 | w=28
  570. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:klippel-trenaunay-weber syndrome
    n1=en:roberts syndrome | n2=en:klippel-trenaunay-weber syndrome | rel=r_associated | relid=0 | w=28
  571. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:landau-kleffner syndrome
    n1=en:roberts syndrome | n2=en:landau-kleffner syndrome | rel=r_associated | relid=0 | w=28
  572. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:lennox-gastaut syndrome
    n1=en:roberts syndrome | n2=en:lennox-gastaut syndrome | rel=r_associated | relid=0 | w=28
  573. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:leprosy
    n1=en:roberts syndrome | n2=en:leprosy | rel=r_associated | relid=0 | w=28
  574. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:leukodystrophy
    n1=en:roberts syndrome | n2=en:leukodystrophy | rel=r_associated | relid=0 | w=28
  575. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:machado-joseph disease
    n1=en:roberts syndrome | n2=en:machado-joseph disease | rel=r_associated | relid=0 | w=28
  576. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:mayer-rokitansky-kuster-hauser syndrome
    n1=en:roberts syndrome | n2=en:mayer-rokitansky-kuster-hauser syndrome | rel=r_associated | relid=0 | w=28
  577. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:microcephaly and chorioretinopathy, autosomal recessive, type 1
    n1=en:roberts syndrome | n2=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | rel=r_associated | relid=0 | w=28
  578. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:mixed connective tissue disease
    n1=en:roberts syndrome | n2=en:mixed connective tissue disease | rel=r_associated | relid=0 | w=28
  579. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:morquio syndrome
    n1=en:roberts syndrome | n2=en:morquio syndrome | rel=r_associated | relid=0 | w=28
  580. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:neurotoxicity syndrome
    n1=en:roberts syndrome | n2=en:neurotoxicity syndrome | rel=r_associated | relid=0 | w=28
  581. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:orofacial cleft 1
    n1=en:roberts syndrome | n2=en:orofacial cleft 1 | rel=r_associated | relid=0 | w=28
  582. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:otopalatodigital syndrome type 1
    n1=en:roberts syndrome | n2=en:otopalatodigital syndrome type 1 | rel=r_associated | relid=0 | w=28
  583. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:pancreatic lipase deficiency
    n1=en:roberts syndrome | n2=en:pancreatic lipase deficiency | rel=r_associated | relid=0 | w=28
  584. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:parinaud syndrome
    n1=en:roberts syndrome | n2=en:parinaud syndrome | rel=r_associated | relid=0 | w=28
  585. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:periodic fever syndrome
    n1=en:roberts syndrome | n2=en:periodic fever syndrome | rel=r_associated | relid=0 | w=28
  586. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:phosphoenolpyruvate carboxykinase deficiency
    n1=en:roberts syndrome | n2=en:phosphoenolpyruvate carboxykinase deficiency | rel=r_associated | relid=0 | w=28
  587. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:pseudoachondroplasia
    n1=en:roberts syndrome | n2=en:pseudoachondroplasia | rel=r_associated | relid=0 | w=28
  588. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:pseudotumor cerebri
    n1=en:roberts syndrome | n2=en:pseudotumor cerebri | rel=r_associated | relid=0 | w=28
  589. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:pyruvate carboxylase deficiency
    n1=en:roberts syndrome | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=28
  590. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:schwartz-jampel syndrome
    n1=en:roberts syndrome | n2=en:schwartz-jampel syndrome | rel=r_associated | relid=0 | w=28
  591. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:scimitar syndrome
    n1=en:roberts syndrome | n2=en:scimitar syndrome | rel=r_associated | relid=0 | w=28
  592. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:selective antibody deficiency with normal immunoglobulins
    n1=en:roberts syndrome | n2=en:selective antibody deficiency with normal immunoglobulins | rel=r_associated | relid=0 | w=28
  593. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:sheehan syndrome
    n1=en:roberts syndrome | n2=en:sheehan syndrome | rel=r_associated | relid=0 | w=28
  594. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:sick sinus syndrome
    n1=en:roberts syndrome | n2=en:sick sinus syndrome | rel=r_associated | relid=0 | w=28
  595. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:stein-leventhal syndrome
    n1=en:roberts syndrome | n2=en:stein-leventhal syndrome | rel=r_associated | relid=0 | w=28
  596. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:stevens-johnson syndrome
    n1=en:roberts syndrome | n2=en:stevens-johnson syndrome | rel=r_associated | relid=0 | w=28
  597. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:sudden unexplained death in childhood
    n1=en:roberts syndrome | n2=en:sudden unexplained death in childhood | rel=r_associated | relid=0 | w=28
  598. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:transient global amnesia
    n1=en:roberts syndrome | n2=en:transient global amnesia | rel=r_associated | relid=0 | w=28
  599. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:true hermaphroditism
    n1=en:roberts syndrome | n2=en:true hermaphroditism | rel=r_associated | relid=0 | w=28
  600. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:twiddler's syndrome
    n1=en:roberts syndrome | n2=en:twiddler's syndrome | rel=r_associated | relid=0 | w=28
  601. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:urea cycle metabolism disorder
    n1=en:roberts syndrome | n2=en:urea cycle metabolism disorder | rel=r_associated | relid=0 | w=28
  602. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:uveomeningoencephalitic syndrome
    n1=en:roberts syndrome | n2=en:uveomeningoencephalitic syndrome | rel=r_associated | relid=0 | w=28
  603. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:wernicke-korsakoff syndrome
    n1=en:roberts syndrome | n2=en:wernicke-korsakoff syndrome | rel=r_associated | relid=0 | w=28
  604. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> en:wiskott-aldrich syndrome
    n1=en:roberts syndrome | n2=en:wiskott-aldrich syndrome | rel=r_associated | relid=0 | w=28
  605. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> maladie de Marfan
    n1=en:roberts syndrome | n2=maladie de Marfan | rel=r_associated | relid=0 | w=28
  606. en:roberts syndrome -- r_associated #0: 28 / 0.651 -> peste
    (maladie)
    n1=en:roberts syndrome | n2=peste
    (maladie)
    | rel=r_associated | relid=0 | w=28
  607. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:1p36 deletion syndrome
    n1=en:roberts syndrome | n2=en:1p36 deletion syndrome | rel=r_associated | relid=0 | w=27
  608. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:5 alpha steroid reductase 2 deficiency
    n1=en:roberts syndrome | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=27
  609. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:acrodermatitis enteropathica
    n1=en:roberts syndrome | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=27
  610. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:alpha thalassemia x-linked mental retardation syndrome
    n1=en:roberts syndrome | n2=en:alpha thalassemia x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=27
  611. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:alpha-methylacyl-coa racemase deficiency
    n1=en:roberts syndrome | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=27
  612. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:alport syndrome
    n1=en:roberts syndrome | n2=en:alport syndrome | rel=r_associated | relid=0 | w=27
  613. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:auditory perceptual disorder
    n1=en:roberts syndrome | n2=en:auditory perceptual disorder | rel=r_associated | relid=0 | w=27
  614. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:autoimmune polyendocrinopathy syndrome
    n1=en:roberts syndrome | n2=en:autoimmune polyendocrinopathy syndrome | rel=r_associated | relid=0 | w=27
  615. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:autosomal dominant optic atrophy
    n1=en:roberts syndrome | n2=en:autosomal dominant optic atrophy | rel=r_associated | relid=0 | w=27
  616. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:bloom syndrome
    n1=en:roberts syndrome | n2=en:bloom syndrome | rel=r_associated | relid=0 | w=27
  617. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:chediak-higashi syndrome
    n1=en:roberts syndrome | n2=en:chediak-higashi syndrome | rel=r_associated | relid=0 | w=27
  618. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:coffin-lowry syndrome
    n1=en:roberts syndrome | n2=en:coffin-lowry syndrome | rel=r_associated | relid=0 | w=27
  619. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:connexin 26 gene anomaly
    n1=en:roberts syndrome | n2=en:connexin 26 gene anomaly | rel=r_associated | relid=0 | w=27
  620. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:cranioectodermal dysplasia
    n1=en:roberts syndrome | n2=en:cranioectodermal dysplasia | rel=r_associated | relid=0 | w=27
  621. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:craniofacial dysostosis
    n1=en:roberts syndrome | n2=en:craniofacial dysostosis | rel=r_associated | relid=0 | w=27
  622. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:cutis laxa
    n1=en:roberts syndrome | n2=en:cutis laxa | rel=r_associated | relid=0 | w=27
  623. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:cystathioninuria
    n1=en:roberts syndrome | n2=en:cystathioninuria | rel=r_associated | relid=0 | w=27
  624. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:dandy-walker malformation
    n1=en:roberts syndrome | n2=en:dandy-walker malformation | rel=r_associated | relid=0 | w=27
  625. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:deafness, autosomal recessive 1a
    n1=en:roberts syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  626. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:dextrocardia
    n1=en:roberts syndrome | n2=en:dextrocardia | rel=r_associated | relid=0 | w=27
  627. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:diffuse infiltrative lymphocytosis syndrome
    n1=en:roberts syndrome | n2=en:diffuse infiltrative lymphocytosis syndrome | rel=r_associated | relid=0 | w=27
  628. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:ectodermal dysplasia
    n1=en:roberts syndrome | n2=en:ectodermal dysplasia | rel=r_associated | relid=0 | w=27
  629. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:felty syndrome
    n1=en:roberts syndrome | n2=en:felty syndrome | rel=r_associated | relid=0 | w=27
  630. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:fetal methotrexate syndrome
    n1=en:roberts syndrome | n2=en:fetal methotrexate syndrome | rel=r_associated | relid=0 | w=27
  631. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:fibromuscular dysplasia
    n1=en:roberts syndrome | n2=en:fibromuscular dysplasia | rel=r_associated | relid=0 | w=27
  632. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:friedreich ataxia
    n1=en:roberts syndrome | n2=en:friedreich ataxia | rel=r_associated | relid=0 | w=27
  633. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:frohlich syndrome
    n1=en:roberts syndrome | n2=en:frohlich syndrome | rel=r_associated | relid=0 | w=27
  634. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:fuchs endothelial dystrophy
    n1=en:roberts syndrome | n2=en:fuchs endothelial dystrophy | rel=r_associated | relid=0 | w=27
  635. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:gynatresia
    n1=en:roberts syndrome | n2=en:gynatresia | rel=r_associated | relid=0 | w=27
  636. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:hemophagocytic syndrome
    n1=en:roberts syndrome | n2=en:hemophagocytic syndrome | rel=r_associated | relid=0 | w=27
  637. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:hmg-coa lyase deficiency
    n1=en:roberts syndrome | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=27
  638. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:holoprosencephaly
    n1=en:roberts syndrome | n2=en:holoprosencephaly | rel=r_associated | relid=0 | w=27
  639. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:horner syndrome
    n1=en:roberts syndrome | n2=en:horner syndrome | rel=r_associated | relid=0 | w=27
  640. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:ichthyosis
    n1=en:roberts syndrome | n2=en:ichthyosis | rel=r_associated | relid=0 | w=27
  641. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:irritable bowel syndrome
    n1=en:roberts syndrome | n2=en:irritable bowel syndrome | rel=r_associated | relid=0 | w=27
  642. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:left ventricular non-compaction syndrome
    n1=en:roberts syndrome | n2=en:left ventricular non-compaction syndrome | rel=r_associated | relid=0 | w=27
  643. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:macrophage activation syndrome
    n1=en:roberts syndrome | n2=en:macrophage activation syndrome | rel=r_associated | relid=0 | w=27
  644. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:malignant atrophic papulosis
    n1=en:roberts syndrome | n2=en:malignant atrophic papulosis | rel=r_associated | relid=0 | w=27
  645. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:meconium aspiration syndrome
    n1=en:roberts syndrome | n2=en:meconium aspiration syndrome | rel=r_associated | relid=0 | w=27
  646. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:melas syndrome
    n1=en:roberts syndrome | n2=en:melas syndrome | rel=r_associated | relid=0 | w=27
  647. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:mitochondrial neurogastrointestingal encephalopathy
    n1=en:roberts syndrome | n2=en:mitochondrial neurogastrointestingal encephalopathy | rel=r_associated | relid=0 | w=27
  648. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:mmih syndrome
    n1=en:roberts syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
  649. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:mowat-wilson syndrome
    n1=en:roberts syndrome | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=27
  650. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:neoplastic syndrome
    n1=en:roberts syndrome | n2=en:neoplastic syndrome | rel=r_associated | relid=0 | w=27
  651. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:nephrotic syndrome
    n1=en:roberts syndrome | n2=en:nephrotic syndrome | rel=r_associated | relid=0 | w=27
  652. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:olivopontocerebellar atrophy
    n1=en:roberts syndrome | n2=en:olivopontocerebellar atrophy | rel=r_associated | relid=0 | w=27
  653. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:opitz g/bbb syndrome
    n1=en:roberts syndrome | n2=en:opitz g/bbb syndrome | rel=r_associated | relid=0 | w=27
  654. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:osteochondrodysplasia
    n1=en:roberts syndrome | n2=en:osteochondrodysplasia | rel=r_associated | relid=0 | w=27
  655. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:pallister-killian syndrome
    n1=en:roberts syndrome | n2=en:pallister-killian syndrome | rel=r_associated | relid=0 | w=27
  656. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:peritoneal panniculitis
    n1=en:roberts syndrome | n2=en:peritoneal panniculitis | rel=r_associated | relid=0 | w=27
  657. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:peters-plus syndrome
    n1=en:roberts syndrome | n2=en:peters-plus syndrome | rel=r_associated | relid=0 | w=27
  658. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:potocki-lupski syndrome
    n1=en:roberts syndrome | n2=en:potocki-lupski syndrome | rel=r_associated | relid=0 | w=27
  659. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:potter syndrome
    n1=en:roberts syndrome | n2=en:potter syndrome | rel=r_associated | relid=0 | w=27
  660. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:pre-excitation syndrome
    n1=en:roberts syndrome | n2=en:pre-excitation syndrome | rel=r_associated | relid=0 | w=27
  661. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:primary carnitine deficiency
    n1=en:roberts syndrome | n2=en:primary carnitine deficiency | rel=r_associated | relid=0 | w=27
  662. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:pseudoxanthoma elasticum
    n1=en:roberts syndrome | n2=en:pseudoxanthoma elasticum | rel=r_associated | relid=0 | w=27
  663. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:rett syndrome
    n1=en:roberts syndrome | n2=en:rett syndrome | rel=r_associated | relid=0 | w=27
  664. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:septo-optic dysplasia
    n1=en:roberts syndrome | n2=en:septo-optic dysplasia | rel=r_associated | relid=0 | w=27
  665. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:shone syndrome
    n1=en:roberts syndrome | n2=en:shone syndrome | rel=r_associated | relid=0 | w=27
  666. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:somnolence syndrome
    n1=en:roberts syndrome | n2=en:somnolence syndrome | rel=r_associated | relid=0 | w=27
  667. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:sotos syndrome
    n1=en:roberts syndrome | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=27
  668. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:subclavian steal syndrome
    n1=en:roberts syndrome | n2=en:subclavian steal syndrome | rel=r_associated | relid=0 | w=27
  669. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:sweet syndrome
    n1=en:roberts syndrome | n2=en:sweet syndrome | rel=r_associated | relid=0 | w=27
  670. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome
    n1=en:roberts syndrome | n2=en:synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome | rel=r_associated | relid=0 | w=27
  671. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:tay-sachs disease
    n1=en:roberts syndrome | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=27
  672. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:trigger finger disorder
    n1=en:roberts syndrome | n2=en:trigger finger disorder | rel=r_associated | relid=0 | w=27
  673. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:tubulointerstitial nephritis and uveitis
    n1=en:roberts syndrome | n2=en:tubulointerstitial nephritis and uveitis | rel=r_associated | relid=0 | w=27
  674. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:vertebral artery syndrome
    n1=en:roberts syndrome | n2=en:vertebral artery syndrome | rel=r_associated | relid=0 | w=27
  675. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:williams syndrome
    n1=en:roberts syndrome | n2=en:williams syndrome | rel=r_associated | relid=0 | w=27
  676. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:wolff-parkinson-white syndrome
    n1=en:roberts syndrome | n2=en:wolff-parkinson-white syndrome | rel=r_associated | relid=0 | w=27
  677. en:roberts syndrome -- r_associated #0: 27 / 0.628 -> en:x-linked bulbar-muscular atrophy
    n1=en:roberts syndrome | n2=en:x-linked bulbar-muscular atrophy | rel=r_associated | relid=0 | w=27
  678. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:abnormal nuclear morphology
    n1=en:roberts syndrome | n2=en:abnormal nuclear morphology | rel=r_associated | relid=0 | w=26
  679. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:abnormality of the pinna
    n1=en:roberts syndrome | n2=en:abnormality of the pinna | rel=r_associated | relid=0 | w=26
  680. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:absence or reduction in length of femur, tibia, or fibula
    n1=en:roberts syndrome | n2=en:absence or reduction in length of femur, tibia, or fibula | rel=r_associated | relid=0 | w=26
  681. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:absence or reduction in length of humerus, radius, or ulna
    n1=en:roberts syndrome | n2=en:absence or reduction in length of humerus, radius, or ulna | rel=r_associated | relid=0 | w=26
  682. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:absent earlobe
    n1=en:roberts syndrome | n2=en:absent earlobe | rel=r_associated | relid=0 | w=26
  683. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:accessory spleen
    n1=en:roberts syndrome | n2=en:accessory spleen | rel=r_associated | relid=0 | w=26
  684. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:acrocallosal syndrome
    n1=en:roberts syndrome | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=26
  685. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:acyl-coa dehydrogenase, short-chain deficiency
    n1=en:roberts syndrome | n2=en:acyl-coa dehydrogenase, short-chain deficiency | rel=r_associated | relid=0 | w=26
  686. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:aicardi syndrome
    n1=en:roberts syndrome | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=26
  687. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:alper syndrome
    n1=en:roberts syndrome | n2=en:alper syndrome | rel=r_associated | relid=0 | w=26
  688. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:ankle contracture
    n1=en:roberts syndrome | n2=en:ankle contracture | rel=r_associated | relid=0 | w=26
  689. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:atrial septal defect
    n1=en:roberts syndrome | n2=en:atrial septal defect | rel=r_associated | relid=0 | w=26
  690. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:autosomal recessive inheritance
    n1=en:roberts syndrome | n2=en:autosomal recessive inheritance | rel=r_associated | relid=0 | w=26
  691. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:beta-methylcrotonylglycinuria
    n1=en:roberts syndrome | n2=en:beta-methylcrotonylglycinuria | rel=r_associated | relid=0 | w=26
  692. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:bicornuate uterus
    n1=en:roberts syndrome | n2=en:bicornuate uterus | rel=r_associated | relid=0 | w=26
  693. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:birth length less than 40cm
    n1=en:roberts syndrome | n2=en:birth length less than 40cm | rel=r_associated | relid=0 | w=26
  694. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:birth weight 1.5-2.2 kg
    n1=en:roberts syndrome | n2=en:birth weight 1.5-2.2 kg | rel=r_associated | relid=0 | w=26
  695. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:blue sclera
    n1=en:roberts syndrome | n2=en:blue sclera | rel=r_associated | relid=0 | w=26
  696. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:brachycephalies
    n1=en:roberts syndrome | n2=en:brachycephalies | rel=r_associated | relid=0 | w=26
  697. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:brachydactyly
    n1=en:roberts syndrome | n2=en:brachydactyly | rel=r_associated | relid=0 | w=26
  698. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:byzanthine arch palate
    n1=en:roberts syndrome | n2=en:byzanthine arch palate | rel=r_associated | relid=0 | w=26
  699. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:cafe au lait spots on trunk and extremities
    n1=en:roberts syndrome | n2=en:cafe au lait spots on trunk and extremities | rel=r_associated | relid=0 | w=26
  700. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:camurati-engelmann syndrome
    n1=en:roberts syndrome | n2=en:camurati-engelmann syndrome | rel=r_associated | relid=0 | w=26
  701. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:cat-eye syndrome
    n1=en:roberts syndrome | n2=en:cat-eye syndrome | rel=r_associated | relid=0 | w=26
  702. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:cataract
    n1=en:roberts syndrome | n2=en:cataract | rel=r_associated | relid=0 | w=26
  703. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:caused by mutation in the establishment of cohesion 1 homolog 2 gene (esco2, 609353.0001)
    n1=en:roberts syndrome | n2=en:caused by mutation in the establishment of cohesion 1 homolog 2 gene (esco2, 609353.0001) | rel=r_associated | relid=0 | w=26
  704. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:cerebrooculofacioskeletal syndrome
    n1=en:roberts syndrome | n2=en:cerebrooculofacioskeletal syndrome | rel=r_associated | relid=0 | w=26
  705. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:chromosome 15q11-q13 duplication syndrome
    n1=en:roberts syndrome | n2=en:chromosome 15q11-q13 duplication syndrome | rel=r_associated | relid=0 | w=26
  706. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:cleft lip
    n1=en:roberts syndrome | n2=en:cleft lip | rel=r_associated | relid=0 | w=26
  707. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:cleft palate
    n1=en:roberts syndrome | n2=en:cleft palate | rel=r_associated | relid=0 | w=26
  708. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:cogan-reese syndrome
    n1=en:roberts syndrome | n2=en:cogan-reese syndrome | rel=r_associated | relid=0 | w=26
  709. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:coloboma of the eyelid
    n1=en:roberts syndrome | n2=en:coloboma of the eyelid | rel=r_associated | relid=0 | w=26
  710. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:complex regional pain syndrome ii
    n1=en:roberts syndrome | n2=en:complex regional pain syndrome ii | rel=r_associated | relid=0 | w=26
  711. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:congenital clinodactyly
    n1=en:roberts syndrome | n2=en:congenital clinodactyly | rel=r_associated | relid=0 | w=26
  712. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:contracture of elbow
    n1=en:roberts syndrome | n2=en:contracture of elbow | rel=r_associated | relid=0 | w=26
  713. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:contracture of knee
    n1=en:roberts syndrome | n2=en:contracture of knee | rel=r_associated | relid=0 | w=26
  714. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:contracture of wrist joint
    n1=en:roberts syndrome | n2=en:contracture of wrist joint | rel=r_associated | relid=0 | w=26
  715. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:corneal haze
    n1=en:roberts syndrome | n2=en:corneal haze | rel=r_associated | relid=0 | w=26
  716. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:cranial nerve palsy
    n1=en:roberts syndrome | n2=en:cranial nerve palsy | rel=r_associated | relid=0 | w=26
  717. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:craniofacial abnormalities
    n1=en:roberts syndrome | n2=en:craniofacial abnormalities | rel=r_associated | relid=0 | w=26
  718. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:craniosynostosis
    n1=en:roberts syndrome | n2=en:craniosynostosis | rel=r_associated | relid=0 | w=26
  719. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:crigler-najjar syndrome
    n1=en:roberts syndrome | n2=en:crigler-najjar syndrome | rel=r_associated | relid=0 | w=26
  720. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:cushing syndrome
    n1=en:roberts syndrome | n2=en:cushing syndrome | rel=r_associated | relid=0 | w=26
  721. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:de sanctis-cacchione syndrome
    n1=en:roberts syndrome | n2=en:de sanctis-cacchione syndrome | rel=r_associated | relid=0 | w=26
  722. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:diethylstilbestrol syndrome
    n1=en:roberts syndrome | n2=en:diethylstilbestrol syndrome | rel=r_associated | relid=0 | w=26
  723. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:diffuse idiopathic skeletal hyperostosis
    n1=en:roberts syndrome | n2=en:diffuse idiopathic skeletal hyperostosis | rel=r_associated | relid=0 | w=26
  724. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:downward slant of palpebral fissure
    n1=en:roberts syndrome | n2=en:downward slant of palpebral fissure | rel=r_associated | relid=0 | w=26
  725. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:ectromelia
    n1=en:roberts syndrome | n2=en:ectromelia | rel=r_associated | relid=0 | w=26
  726. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:encephaloceles, frontal
    n1=en:roberts syndrome | n2=en:encephaloceles, frontal | rel=r_associated | relid=0 | w=26
  727. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:enlarged labia minora
    n1=en:roberts syndrome | n2=en:enlarged labia minora | rel=r_associated | relid=0 | w=26
  728. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:esco2, 1-bp ins, 750g
    n1=en:roberts syndrome | n2=en:esco2, 1-bp ins, 750g | rel=r_associated | relid=0 | w=26
  729. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:esco2, arg169ter
    n1=en:roberts syndrome | n2=en:esco2, arg169ter | rel=r_associated | relid=0 | w=26
  730. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:esco2, trp539gly
    n1=en:roberts syndrome | n2=en:esco2, trp539gly | rel=r_associated | relid=0 | w=26
  731. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:exophthalmos
    n1=en:roberts syndrome | n2=en:exophthalmos | rel=r_associated | relid=0 | w=26
  732. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:fibromyalgia
    n1=en:roberts syndrome | n2=en:fibromyalgia | rel=r_associated | relid=0 | w=26
  733. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:freeman-sheldon syndrome
    n1=en:roberts syndrome | n2=en:freeman-sheldon syndrome | rel=r_associated | relid=0 | w=26
  734. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:frontonasal dysplasia
    n1=en:roberts syndrome | n2=en:frontonasal dysplasia | rel=r_associated | relid=0 | w=26
  735. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:fusion of metacarpal bones
    n1=en:roberts syndrome | n2=en:fusion of metacarpal bones | rel=r_associated | relid=0 | w=26
  736. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:gilbert syndrome
    n1=en:roberts syndrome | n2=en:gilbert syndrome | rel=r_associated | relid=0 | w=26
  737. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:glutaric acidemia type 1
    n1=en:roberts syndrome | n2=en:glutaric acidemia type 1 | rel=r_associated | relid=0 | w=26
  738. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:gray platelet syndrome
    n1=en:roberts syndrome | n2=en:gray platelet syndrome | rel=r_associated | relid=0 | w=26
  739. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:hemochromatosis
    n1=en:roberts syndrome | n2=en:hemochromatosis | rel=r_associated | relid=0 | w=26
  740. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:horseshoe kidney
    n1=en:roberts syndrome | n2=en:horseshoe kidney | rel=r_associated | relid=0 | w=26
  741. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:hurler-scheie syndrome
    n1=en:roberts syndrome | n2=en:hurler-scheie syndrome | rel=r_associated | relid=0 | w=26
  742. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:hydrocephalus
    n1=en:roberts syndrome | n2=en:hydrocephalus | rel=r_associated | relid=0 | w=26
  743. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:hyperkalemic periodic paralysis
    n1=en:roberts syndrome | n2=en:hyperkalemic periodic paralysis | rel=r_associated | relid=0 | w=26
  744. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:hypertelorism
    n1=en:roberts syndrome | n2=en:hypertelorism | rel=r_associated | relid=0 | w=26
  745. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:hypertrophy of clitoris
    n1=en:roberts syndrome | n2=en:hypertrophy of clitoris | rel=r_associated | relid=0 | w=26
  746. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:hypomelia (more severe in upper limbs)
    n1=en:roberts syndrome | n2=en:hypomelia (more severe in upper limbs) | rel=r_associated | relid=0 | w=26
  747. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:hypospadias
    n1=en:roberts syndrome | n2=en:hypospadias | rel=r_associated | relid=0 | w=26
  748. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:immune reconstitution inflammatory syndrome associated with kaposi sarcoma
    n1=en:roberts syndrome | n2=en:immune reconstitution inflammatory syndrome associated with kaposi sarcoma | rel=r_associated | relid=0 | w=26
  749. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:increased size of penis
    n1=en:roberts syndrome | n2=en:increased size of penis | rel=r_associated | relid=0 | w=26
  750. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:karyotype analysis normal finding
    n1=en:roberts syndrome | n2=en:karyotype analysis normal finding | rel=r_associated | relid=0 | w=26
  751. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:kleine-levin syndrome
    n1=en:roberts syndrome | n2=en:kleine-levin syndrome | rel=r_associated | relid=0 | w=26
  752. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:kniest dysplasia
    n1=en:roberts syndrome | n2=en:kniest dysplasia | rel=r_associated | relid=0 | w=26
  753. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:kshv inflammatory cytokine syndrome
    n1=en:roberts syndrome | n2=en:kshv inflammatory cytokine syndrome | rel=r_associated | relid=0 | w=26
  754. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:lecithin acyltransferase deficiency
    n1=en:roberts syndrome | n2=en:lecithin acyltransferase deficiency | rel=r_associated | relid=0 | w=26
  755. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:leigh disease
    n1=en:roberts syndrome | n2=en:leigh disease | rel=r_associated | relid=0 | w=26
  756. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:leopard syndrome
    n1=en:roberts syndrome | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=26
  757. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:liddle syndrome
    n1=en:roberts syndrome | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=26
  758. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:lig4 syndrome
    n1=en:roberts syndrome | n2=en:lig4 syndrome | rel=r_associated | relid=0 | w=26
  759. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:likely allelic to sc phocomelia syndrome (269000)
    n1=en:roberts syndrome | n2=en:likely allelic to sc phocomelia syndrome (269000) | rel=r_associated | relid=0 | w=26
  760. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:lissencephaly
    n1=en:roberts syndrome | n2=en:lissencephaly | rel=r_associated | relid=0 | w=26
  761. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:low set ears
    n1=en:roberts syndrome | n2=en:low set ears | rel=r_associated | relid=0 | w=26
  762. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:malakoplakia
    n1=en:roberts syndrome | n2=en:malakoplakia | rel=r_associated | relid=0 | w=26
  763. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:malar flattening
    n1=en:roberts syndrome | n2=en:malar flattening | rel=r_associated | relid=0 | w=26
  764. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:meckel-gruber syndrome
    n1=en:roberts syndrome | n2=en:meckel-gruber syndrome | rel=r_associated | relid=0 | w=26
  765. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:medium-chain acyl-coa dehydrogenase deficiency
    n1=en:roberts syndrome | n2=en:medium-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=26
  766. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:meningeal tuberculosis
    n1=en:roberts syndrome | n2=en:meningeal tuberculosis | rel=r_associated | relid=0 | w=26
  767. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:mental retardation
    n1=en:roberts syndrome | n2=en:mental retardation | rel=r_associated | relid=0 | w=26
  768. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:microcephaly
    n1=en:roberts syndrome | n2=en:microcephaly | rel=r_associated | relid=0 | w=26
  769. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:micrognathism
    n1=en:roberts syndrome | n2=en:micrognathism | rel=r_associated | relid=0 | w=26
  770. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:microphthalmos
    n1=en:roberts syndrome | n2=en:microphthalmos | rel=r_associated | relid=0 | w=26
  771. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:midface capillary hemangioma
    n1=en:roberts syndrome | n2=en:midface capillary hemangioma | rel=r_associated | relid=0 | w=26
  772. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:migrating partial seizures in infancy
    n1=en:roberts syndrome | n2=en:migrating partial seizures in infancy | rel=r_associated | relid=0 | w=26
  773. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:mild-severe postnatal growth deficiency
    n1=en:roberts syndrome | n2=en:mild-severe postnatal growth deficiency | rel=r_associated | relid=0 | w=26
  774. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:mobius syndrome
    n1=en:roberts syndrome | n2=en:mobius syndrome | rel=r_associated | relid=0 | w=26
  775. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:multiple acyl-coa dehydrogenase deficiency
    n1=en:roberts syndrome | n2=en:multiple acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=26
  776. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:myotonic disorder
    n1=en:roberts syndrome | n2=en:myotonic disorder | rel=r_associated | relid=0 | w=26
  777. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:nail-patella syndrome
    n1=en:roberts syndrome | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=26
  778. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:narrow naris
    n1=en:roberts syndrome | n2=en:narrow naris | rel=r_associated | relid=0 | w=26
  779. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:nephrogenic fibrosing dermopathy
    n1=en:roberts syndrome | n2=en:nephrogenic fibrosing dermopathy | rel=r_associated | relid=0 | w=26
  780. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:neuropathy, hereditary sensory and autonomic, type vii
    n1=en:roberts syndrome | n2=en:neuropathy, hereditary sensory and autonomic, type vii | rel=r_associated | relid=0 | w=26
  781. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:nuchal cystic hygroma
    n1=en:roberts syndrome | n2=en:nuchal cystic hygroma | rel=r_associated | relid=0 | w=26
  782. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:ochronosis
    n1=en:roberts syndrome | n2=en:ochronosis | rel=r_associated | relid=0 | w=26
  783. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:oligodactyly
    n1=en:roberts syndrome | n2=en:oligodactyly | rel=r_associated | relid=0 | w=26
  784. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:paragonimiasis
    n1=en:roberts syndrome | n2=en:paragonimiasis | rel=r_associated | relid=0 | w=26
  785. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:patent ductus arteriosus
    n1=en:roberts syndrome | n2=en:patent ductus arteriosus | rel=r_associated | relid=0 | w=26
  786. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:pelizaeus-merzbacher disease
    n1=en:roberts syndrome | n2=en:pelizaeus-merzbacher disease | rel=r_associated | relid=0 | w=26
  787. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:pemphigoid gestationis
    n1=en:roberts syndrome | n2=en:pemphigoid gestationis | rel=r_associated | relid=0 | w=26
  788. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:persistent fetal circulation
    n1=en:roberts syndrome | n2=en:persistent fetal circulation | rel=r_associated | relid=0 | w=26
  789. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:piriformis muscle syndrome
    n1=en:roberts syndrome | n2=en:piriformis muscle syndrome | rel=r_associated | relid=0 | w=26
  790. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:polycystic kidney - body part
    n1=en:roberts syndrome | n2=en:polycystic kidney - body part | rel=r_associated | relid=0 | w=26
  791. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:polyhydramnios
    n1=en:roberts syndrome | n2=en:polyhydramnios | rel=r_associated | relid=0 | w=26
  792. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:posterior fossa syndrome
    n1=en:roberts syndrome | n2=en:posterior fossa syndrome | rel=r_associated | relid=0 | w=26
  793. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:posteriorly rotated ear
    n1=en:roberts syndrome | n2=en:posteriorly rotated ear | rel=r_associated | relid=0 | w=26
  794. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:premature separation of centromeric heterochromatin
    n1=en:roberts syndrome | n2=en:premature separation of centromeric heterochromatin | rel=r_associated | relid=0 | w=26
  795. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:presence of severe midfacial and limb defects and birth length less than 37cm associated with stillborn or early infant death
    n1=en:roberts syndrome | n2=en:presence of severe midfacial and limb defects and birth length less than 37cm associated with stillborn or early infant death | rel=r_associated | relid=0 | w=26
  796. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:primary hypertrophic osteoarthropathy
    n1=en:roberts syndrome | n2=en:primary hypertrophic osteoarthropathy | rel=r_associated | relid=0 | w=26
  797. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:progressive familial intrahepatic cholestasis
    n1=en:roberts syndrome | n2=en:progressive familial intrahepatic cholestasis | rel=r_associated | relid=0 | w=26
  798. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:prominent eyes
    n1=en:roberts syndrome | n2=en:prominent eyes | rel=r_associated | relid=0 | w=26
  799. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:proteus syndrome
    n1=en:roberts syndrome | n2=en:proteus syndrome | rel=r_associated | relid=0 | w=26
  800. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:pseudohermaphroditism
    n1=en:roberts syndrome | n2=en:pseudohermaphroditism | rel=r_associated | relid=0 | w=26
  801. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:pseudohypoaldosteronism
    n1=en:roberts syndrome | n2=en:pseudohypoaldosteronism | rel=r_associated | relid=0 | w=26
  802. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:pulmonary alveolar proteinosis
    n1=en:roberts syndrome | n2=en:pulmonary alveolar proteinosis | rel=r_associated | relid=0 | w=26
  803. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:radial aplasia-thrombocytopenia syndrome
    n1=en:roberts syndrome | n2=en:radial aplasia-thrombocytopenia syndrome | rel=r_associated | relid=0 | w=26
  804. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:radiation sickness syndrome
    n1=en:roberts syndrome | n2=en:radiation sickness syndrome | rel=r_associated | relid=0 | w=26
  805. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:reduction in number of toes
    n1=en:roberts syndrome | n2=en:reduction in number of toes | rel=r_associated | relid=0 | w=26
  806. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:respiratory distress syndrome
    n1=en:roberts syndrome | n2=en:respiratory distress syndrome | rel=r_associated | relid=0 | w=26
  807. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:roberts-sc phocomelia syndrome
    n1=en:roberts syndrome | n2=en:roberts-sc phocomelia syndrome | rel=r_associated | relid=0 | w=26
  808. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:rudimentary gallbladder
    n1=en:roberts syndrome | n2=en:rudimentary gallbladder | rel=r_associated | relid=0 | w=26
  809. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:sea-blue histiocyte syndrome
    n1=en:roberts syndrome | n2=en:sea-blue histiocyte syndrome | rel=r_associated | relid=0 | w=26
  810. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:severe intrauterine growth retardation
    n1=en:roberts syndrome | n2=en:severe intrauterine growth retardation | rel=r_associated | relid=0 | w=26
  811. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:shallow orbits
    n1=en:roberts syndrome | n2=en:shallow orbits | rel=r_associated | relid=0 | w=26
  812. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:short neck
    n1=en:roberts syndrome | n2=en:short neck | rel=r_associated | relid=0 | w=26
  813. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:shy-drager syndrome
    n1=en:roberts syndrome | n2=en:shy-drager syndrome | rel=r_associated | relid=0 | w=26
  814. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:sick euthyroid syndrome
    n1=en:roberts syndrome | n2=en:sick euthyroid syndrome | rel=r_associated | relid=0 | w=26
  815. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:silvery blonde scalp hair
    n1=en:roberts syndrome | n2=en:silvery blonde scalp hair | rel=r_associated | relid=0 | w=26
  816. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:sitosterolemia
    n1=en:roberts syndrome | n2=en:sitosterolemia | rel=r_associated | relid=0 | w=26
  817. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:sparse hair
    n1=en:roberts syndrome | n2=en:sparse hair | rel=r_associated | relid=0 | w=26
  818. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:spondyloepimetaphyseal dysplasia, sponastrime type
    n1=en:roberts syndrome | n2=en:spondyloepimetaphyseal dysplasia, sponastrime type | rel=r_associated | relid=0 | w=26
  819. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:stiff person syndrome
    n1=en:roberts syndrome | n2=en:stiff person syndrome | rel=r_associated | relid=0 | w=26
  820. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:superior mesenteric artery syndrome
    n1=en:roberts syndrome | n2=en:superior mesenteric artery syndrome | rel=r_associated | relid=0 | w=26
  821. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:syndactyly
    n1=en:roberts syndrome | n2=en:syndactyly | rel=r_associated | relid=0 | w=26
  822. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:syndrome of apparent mineralocorticoid excess
    n1=en:roberts syndrome | n2=en:syndrome of apparent mineralocorticoid excess | rel=r_associated | relid=0 | w=26
  823. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:talipes equinovalgus
    n1=en:roberts syndrome | n2=en:talipes equinovalgus | rel=r_associated | relid=0 | w=26
  824. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:tethered spinal cord syndrome
    n1=en:roberts syndrome | n2=en:tethered spinal cord syndrome | rel=r_associated | relid=0 | w=26
  825. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:tetraphocomelia
    n1=en:roberts syndrome | n2=en:tetraphocomelia | rel=r_associated | relid=0 | w=26
  826. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:thanatophoric dysplasia
    n1=en:roberts syndrome | n2=en:thanatophoric dysplasia | rel=r_associated | relid=0 | w=26
  827. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:tracheobronchomalacia
    n1=en:roberts syndrome | n2=en:tracheobronchomalacia | rel=r_associated | relid=0 | w=26
  828. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:underdeveloped nasal alae
    n1=en:roberts syndrome | n2=en:underdeveloped nasal alae | rel=r_associated | relid=0 | w=26
  829. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:undescended testes
    n1=en:roberts syndrome | n2=en:undescended testes | rel=r_associated | relid=0 | w=26
  830. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:ventricular septal defect
    n1=en:roberts syndrome | n2=en:ventricular septal defect | rel=r_associated | relid=0 | w=26
  831. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:waardenburg syndrome
    n1=en:roberts syndrome | n2=en:waardenburg syndrome | rel=r_associated | relid=0 | w=26
  832. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:walker-warburg syndrome
    n1=en:roberts syndrome | n2=en:walker-warburg syndrome | rel=r_associated | relid=0 | w=26
  833. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:wegener granulomatosis
    n1=en:roberts syndrome | n2=en:wegener granulomatosis | rel=r_associated | relid=0 | w=26
  834. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> en:wide nasal bridge
    n1=en:roberts syndrome | n2=en:wide nasal bridge | rel=r_associated | relid=0 | w=26
  835. en:roberts syndrome -- r_associated #0: 26 / 0.605 -> syndrome
    n1=en:roberts syndrome | n2=syndrome | rel=r_associated | relid=0 | w=26
  836. en:roberts syndrome -- r_associated #0: 22 / 0.512 -> syndrome de Marfan
    n1=en:roberts syndrome | n2=syndrome de Marfan | rel=r_associated | relid=0 | w=22
  837. en:roberts syndrome -- r_associated #0: 21 / 0.488 -> syndrome de Walker-Warburg
    n1=en:roberts syndrome | n2=syndrome de Walker-Warburg | rel=r_associated | relid=0 | w=21
  838. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> acidémie glutarique de type 1
    n1=en:roberts syndrome | n2=acidémie glutarique de type 1 | rel=r_associated | relid=0 | w=20
  839. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> acidurie glutarique de type 1
    n1=en:roberts syndrome | n2=acidurie glutarique de type 1 | rel=r_associated | relid=0 | w=20
  840. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> acrodermatite entéropathique
    n1=en:roberts syndrome | n2=acrodermatite entéropathique | rel=r_associated | relid=0 | w=20
  841. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> acromégalie
    n1=en:roberts syndrome | n2=acromégalie | rel=r_associated | relid=0 | w=20
  842. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> acromégalie, plis cutanés de la face et du cuir chevelu, et leucomes cornéens
    n1=en:roberts syndrome | n2=acromégalie, plis cutanés de la face et du cuir chevelu, et leucomes cornéens | rel=r_associated | relid=0 | w=20
  843. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> acromegaly
    n1=en:roberts syndrome | n2=acromegaly | rel=r_associated | relid=0 | w=20
  844. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> agnosie
    n1=en:roberts syndrome | n2=agnosie | rel=r_associated | relid=0 | w=20
  845. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> aïnhum
    n1=en:roberts syndrome | n2=aïnhum | rel=r_associated | relid=0 | w=20
  846. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ainhum
    n1=en:roberts syndrome | n2=ainhum | rel=r_associated | relid=0 | w=20
  847. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> albinisme
    n1=en:roberts syndrome | n2=albinisme | rel=r_associated | relid=0 | w=20
  848. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> albinisme oculocutané de type mutant jaune
    n1=en:roberts syndrome | n2=albinisme oculocutané de type mutant jaune | rel=r_associated | relid=0 | w=20
  849. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> alvéolite
    n1=en:roberts syndrome | n2=alvéolite | rel=r_associated | relid=0 | w=20
  850. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> anasarque foetal
    n1=en:roberts syndrome | n2=anasarque foetal | rel=r_associated | relid=0 | w=20
  851. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> anasarque foeto-placentaire
    n1=en:roberts syndrome | n2=anasarque foeto-placentaire | rel=r_associated | relid=0 | w=20
  852. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> anasarque foetoplacentaire
    n1=en:roberts syndrome | n2=anasarque foetoplacentaire | rel=r_associated | relid=0 | w=20
  853. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> anencéphalie
    n1=en:roberts syndrome | n2=anencéphalie | rel=r_associated | relid=0 | w=20
  854. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> aniridie, ataxie cérébelleuse et déficience mentale
    n1=en:roberts syndrome | n2=aniridie, ataxie cérébelleuse et déficience mentale | rel=r_associated | relid=0 | w=20
  855. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> anomalie d'Ebstein
    n1=en:roberts syndrome | n2=anomalie d'Ebstein | rel=r_associated | relid=0 | w=20
  856. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> anomalie du septum auriculaire
    n1=en:roberts syndrome | n2=anomalie du septum auriculaire | rel=r_associated | relid=0 | w=20
  857. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> anti-sida
    n1=en:roberts syndrome | n2=anti-sida | rel=r_associated | relid=0 | w=20
  858. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> antisida
    n1=en:roberts syndrome | n2=antisida | rel=r_associated | relid=0 | w=20
  859. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> aphasie primaire progressive
    n1=en:roberts syndrome | n2=aphasie primaire progressive | rel=r_associated | relid=0 | w=20
  860. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> aphasie progressive primaire
    n1=en:roberts syndrome | n2=aphasie progressive primaire | rel=r_associated | relid=0 | w=20
  861. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> aphasies primaires progressives
    n1=en:roberts syndrome | n2=aphasies primaires progressives | rel=r_associated | relid=0 | w=20
  862. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> arachnodactylie
    n1=en:roberts syndrome | n2=arachnodactylie | rel=r_associated | relid=0 | w=20
  863. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> arriération
    n1=en:roberts syndrome | n2=arriération | rel=r_associated | relid=0 | w=20
  864. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> arriération mentale
    n1=en:roberts syndrome | n2=arriération mentale | rel=r_associated | relid=0 | w=20
  865. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> arthrogrypose
    n1=en:roberts syndrome | n2=arthrogrypose | rel=r_associated | relid=0 | w=20
  866. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> association toxoplasmose, rubéole, cytomégalovirus et herpès chez un nouveau-né
    n1=en:roberts syndrome | n2=association toxoplasmose, rubéole, cytomégalovirus et herpès chez un nouveau-né | rel=r_associated | relid=0 | w=20
  867. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> atélectasie congestive
    n1=en:roberts syndrome | n2=atélectasie congestive | rel=r_associated | relid=0 | w=20
  868. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> atransferrinémie
    n1=en:roberts syndrome | n2=atransferrinémie | rel=r_associated | relid=0 | w=20
  869. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> atrophie optique autosomique dominante
    n1=en:roberts syndrome | n2=atrophie optique autosomique dominante | rel=r_associated | relid=0 | w=20
  870. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> brachydactylie
    n1=en:roberts syndrome | n2=brachydactylie | rel=r_associated | relid=0 | w=20
  871. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> cataplexie
    n1=en:roberts syndrome | n2=cataplexie | rel=r_associated | relid=0 | w=20
  872. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie
    n1=en:roberts syndrome | n2=cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie | rel=r_associated | relid=0 | w=20
  873. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> cétoacidurie à chaînes ramifiées
    n1=en:roberts syndrome | n2=cétoacidurie à chaînes ramifiées | rel=r_associated | relid=0 | w=20
  874. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> choc au poumon
    n1=en:roberts syndrome | n2=choc au poumon | rel=r_associated | relid=0 | w=20
  875. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> choc toxique
    n1=en:roberts syndrome | n2=choc toxique | rel=r_associated | relid=0 | w=20
  876. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> choc toxique staphylococcique
    n1=en:roberts syndrome | n2=choc toxique staphylococcique | rel=r_associated | relid=0 | w=20
  877. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> cholestase intrahépatique progressive familiale de type 1
    n1=en:roberts syndrome | n2=cholestase intrahépatique progressive familiale de type 1 | rel=r_associated | relid=0 | w=20
  878. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> cholestases intrahépatiques progressives familiales
    n1=en:roberts syndrome | n2=cholestases intrahépatiques progressives familiales | rel=r_associated | relid=0 | w=20
  879. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> chondrodysplasia punctata
    n1=en:roberts syndrome | n2=chondrodysplasia punctata | rel=r_associated | relid=0 | w=20
  880. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> coarctation aortique
    n1=en:roberts syndrome | n2=coarctation aortique | rel=r_associated | relid=0 | w=20
  881. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> communication inter-auriculaire
    n1=en:roberts syndrome | n2=communication inter-auriculaire | rel=r_associated | relid=0 | w=20
  882. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> communication interauriculaire
    n1=en:roberts syndrome | n2=communication interauriculaire | rel=r_associated | relid=0 | w=20
  883. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> crânio-sténose
    n1=en:roberts syndrome | n2=crânio-sténose | rel=r_associated | relid=0 | w=20
  884. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> craniosténose
    n1=en:roberts syndrome | n2=craniosténose | rel=r_associated | relid=0 | w=20
  885. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> crâniosténose
    n1=en:roberts syndrome | n2=crâniosténose | rel=r_associated | relid=0 | w=20
  886. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> craniosynostose
    n1=en:roberts syndrome | n2=craniosynostose | rel=r_associated | relid=0 | w=20
  887. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> crâniosynostose
    n1=en:roberts syndrome | n2=crâniosynostose | rel=r_associated | relid=0 | w=20
  888. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> cysticercose
    n1=en:roberts syndrome | n2=cysticercose | rel=r_associated | relid=0 | w=20
  889. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> cysticercose cérébrale
    n1=en:roberts syndrome | n2=cysticercose cérébrale | rel=r_associated | relid=0 | w=20
  890. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> cysticercose du système nerveux central
    n1=en:roberts syndrome | n2=cysticercose du système nerveux central | rel=r_associated | relid=0 | w=20
  891. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> cysticercose neurologique
    n1=en:roberts syndrome | n2=cysticercose neurologique | rel=r_associated | relid=0 | w=20
  892. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> cysticercoses
    n1=en:roberts syndrome | n2=cysticercoses | rel=r_associated | relid=0 | w=20
  893. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> débilité mentale
    n1=en:roberts syndrome | n2=débilité mentale | rel=r_associated | relid=0 | w=20
  894. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> déficience intellectuelle
    n1=en:roberts syndrome | n2=déficience intellectuelle | rel=r_associated | relid=0 | w=20
  895. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> déficience mentale
    n1=en:roberts syndrome | n2=déficience mentale | rel=r_associated | relid=0 | w=20
  896. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> déficit congénital en mégacaryocytes
    n1=en:roberts syndrome | n2=déficit congénital en mégacaryocytes | rel=r_associated | relid=0 | w=20
  897. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> déficit en biotinidase
    n1=en:roberts syndrome | n2=déficit en biotinidase | rel=r_associated | relid=0 | w=20
  898. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> déficit en céto-acide décarboxylase
    n1=en:roberts syndrome | n2=déficit en céto-acide décarboxylase | rel=r_associated | relid=0 | w=20
  899. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> déficit en cytochrome oxydase
    n1=en:roberts syndrome | n2=déficit en cytochrome oxydase | rel=r_associated | relid=0 | w=20
  900. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> déficit en cytochrome-c oxydase
    n1=en:roberts syndrome | n2=déficit en cytochrome-c oxydase | rel=r_associated | relid=0 | w=20
  901. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> déficit en prolidase
    n1=en:roberts syndrome | n2=déficit en prolidase | rel=r_associated | relid=0 | w=20
  902. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> déficit en protéine trifonctionnelle mitochondriale
    n1=en:roberts syndrome | n2=déficit en protéine trifonctionnelle mitochondriale | rel=r_associated | relid=0 | w=20
  903. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> déficit en pyruvate carboxylase
    n1=en:roberts syndrome | n2=déficit en pyruvate carboxylase | rel=r_associated | relid=0 | w=20
  904. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dégénérescence wallérienne
    n1=en:roberts syndrome | n2=dégénérescence wallérienne | rel=r_associated | relid=0 | w=20
  905. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> démence fronto-temporale
    n1=en:roberts syndrome | n2=démence fronto-temporale | rel=r_associated | relid=0 | w=20
  906. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> démence frontotemporale
    n1=en:roberts syndrome | n2=démence frontotemporale | rel=r_associated | relid=0 | w=20
  907. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dentine opalescente héréditaire
    n1=en:roberts syndrome | n2=dentine opalescente héréditaire | rel=r_associated | relid=0 | w=20
  908. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dentinogénèse imparfaite
    n1=en:roberts syndrome | n2=dentinogénèse imparfaite | rel=r_associated | relid=0 | w=20
  909. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> DentinoGenesis Imperfecta
    n1=en:roberts syndrome | n2=DentinoGenesis Imperfecta | rel=r_associated | relid=0 | w=20
  910. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dentinogenesis imperfecta
    n1=en:roberts syndrome | n2=dentinogenesis imperfecta | rel=r_associated | relid=0 | w=20
  911. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> détresse respiratoire
    n1=en:roberts syndrome | n2=détresse respiratoire | rel=r_associated | relid=0 | w=20
  912. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dextrocardie
    n1=en:roberts syndrome | n2=dextrocardie | rel=r_associated | relid=0 | w=20
  913. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> distomatoses pulmonaires
    n1=en:roberts syndrome | n2=distomatoses pulmonaires | rel=r_associated | relid=0 | w=20
  914. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Duane (syndrome de)
    n1=en:roberts syndrome | n2=Duane (syndrome de) | rel=r_associated | relid=0 | w=20
  915. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dumping syndrome
    n1=en:roberts syndrome | n2=dumping syndrome | rel=r_associated | relid=0 | w=20
  916. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dysérythropoïèse congénitale
    n1=en:roberts syndrome | n2=dysérythropoïèse congénitale | rel=r_associated | relid=0 | w=20
  917. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dysostose craniofaciale
    n1=en:roberts syndrome | n2=dysostose craniofaciale | rel=r_associated | relid=0 | w=20
  918. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dysplasie campomélique
    n1=en:roberts syndrome | n2=dysplasie campomélique | rel=r_associated | relid=0 | w=20
  919. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dysplasie cléido-crânienne
    n1=en:roberts syndrome | n2=dysplasie cléido-crânienne | rel=r_associated | relid=0 | w=20
  920. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dysplasie cléidocrânienne
    n1=en:roberts syndrome | n2=dysplasie cléidocrânienne | rel=r_associated | relid=0 | w=20
  921. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dysplasie ectodermique
    n1=en:roberts syndrome | n2=dysplasie ectodermique | rel=r_associated | relid=0 | w=20
  922. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental
    n1=en:roberts syndrome | n2=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | rel=r_associated | relid=0 | w=20
  923. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dysplasie ectodermique, ectrodactylie et dystrophie maculaire
    n1=en:roberts syndrome | n2=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | rel=r_associated | relid=0 | w=20
  924. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dysplasie frontonasale
    n1=en:roberts syndrome | n2=dysplasie frontonasale | rel=r_associated | relid=0 | w=20
  925. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dystrophie neuro-axonale infantile
    n1=en:roberts syndrome | n2=dystrophie neuro-axonale infantile | rel=r_associated | relid=0 | w=20
  926. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dystrophie neuroaxonale
    n1=en:roberts syndrome | n2=dystrophie neuroaxonale | rel=r_associated | relid=0 | w=20
  927. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dystrophie neuroaxonale de Seitelberger
    n1=en:roberts syndrome | n2=dystrophie neuroaxonale de Seitelberger | rel=r_associated | relid=0 | w=20
  928. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dystrophie neuroaxonale infantile
    n1=en:roberts syndrome | n2=dystrophie neuroaxonale infantile | rel=r_associated | relid=0 | w=20
  929. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dystrophie orbitaire congénitale
    n1=en:roberts syndrome | n2=dystrophie orbitaire congénitale | rel=r_associated | relid=0 | w=20
  930. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> dystrophies neuroaxonales
    n1=en:roberts syndrome | n2=dystrophies neuroaxonales | rel=r_associated | relid=0 | w=20
  931. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie)
    n1=en:roberts syndrome | n2=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | rel=r_associated | relid=0 | w=20
  932. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ectrodactylie
    n1=en:roberts syndrome | n2=ectrodactylie | rel=r_associated | relid=0 | w=20
  933. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:10p13-p14 deletion syndrome
    n1=en:roberts syndrome | n2=en:10p13-p14 deletion syndrome | rel=r_associated | relid=0 | w=20
  934. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:acrodysostosis 1
    n1=en:roberts syndrome | n2=en:acrodysostosis 1 | rel=r_associated | relid=0 | w=20
  935. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:adenocutanemucous syndrome
    n1=en:roberts syndrome | n2=en:adenocutanemucous syndrome | rel=r_associated | relid=0 | w=20
  936. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:aids
    n1=en:roberts syndrome | n2=en:aids | rel=r_associated | relid=0 | w=20
  937. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:AIDS
    n1=en:roberts syndrome | n2=en:AIDS | rel=r_associated | relid=0 | w=20
  938. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:AIDS awareness
    n1=en:roberts syndrome | n2=en:AIDS awareness | rel=r_associated | relid=0 | w=20
  939. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Alagille's syndrome
    n1=en:roberts syndrome | n2=en:Alagille's syndrome | rel=r_associated | relid=0 | w=20
  940. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Alice in Wonderland syndrome
    n1=en:roberts syndrome | n2=en:Alice in Wonderland syndrome | rel=r_associated | relid=0 | w=20
  941. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Alice in wonderland Syndrome
    n1=en:roberts syndrome | n2=en:Alice in wonderland Syndrome | rel=r_associated | relid=0 | w=20
  942. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:alligator skin
    n1=en:roberts syndrome | n2=en:alligator skin | rel=r_associated | relid=0 | w=20
  943. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:alveolar proteinosis
    n1=en:roberts syndrome | n2=en:alveolar proteinosis | rel=r_associated | relid=0 | w=20
  944. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:amyoplasia congenita
    n1=en:roberts syndrome | n2=en:amyoplasia congenita | rel=r_associated | relid=0 | w=20
  945. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:anaerosis
    n1=en:roberts syndrome | n2=en:anaerosis | rel=r_associated | relid=0 | w=20
  946. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:anal imperforation
    n1=en:roberts syndrome | n2=en:anal imperforation | rel=r_associated | relid=0 | w=20
  947. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:and mental retardation
    n1=en:roberts syndrome | n2=en:and mental retardation | rel=r_associated | relid=0 | w=20
  948. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Angelman syndrome
    n1=en:roberts syndrome | n2=en:Angelman syndrome | rel=r_associated | relid=0 | w=20
  949. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:anti-AIDS
    n1=en:roberts syndrome | n2=en:anti-AIDS | rel=r_associated | relid=0 | w=20
  950. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:arachnodactyly
    n1=en:roberts syndrome | n2=en:arachnodactyly | rel=r_associated | relid=0 | w=20
  951. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:arnold chiari malformation
    n1=en:roberts syndrome | n2=en:arnold chiari malformation | rel=r_associated | relid=0 | w=20
  952. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:arnold-chiari deformity
    n1=en:roberts syndrome | n2=en:arnold-chiari deformity | rel=r_associated | relid=0 | w=20
  953. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:ataxia-telangiectasisa-like disorder 1
    n1=en:roberts syndrome | n2=en:ataxia-telangiectasisa-like disorder 1 | rel=r_associated | relid=0 | w=20
  954. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:autoimmune polyglandular syndrome
    n1=en:roberts syndrome | n2=en:autoimmune polyglandular syndrome | rel=r_associated | relid=0 | w=20
  955. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:autosomal dominant congenital deafness with onychodystrophy
    n1=en:roberts syndrome | n2=en:autosomal dominant congenital deafness with onychodystrophy | rel=r_associated | relid=0 | w=20
  956. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:black death
    n1=en:roberts syndrome | n2=en:black death | rel=r_associated | relid=0 | w=20
  957. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Black death
    n1=en:roberts syndrome | n2=en:Black death | rel=r_associated | relid=0 | w=20
  958. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:black plague
    n1=en:roberts syndrome | n2=en:black plague | rel=r_associated | relid=0 | w=20
  959. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:branched-chain ketoaciduria
    n1=en:roberts syndrome | n2=en:branched-chain ketoaciduria | rel=r_associated | relid=0 | w=20
  960. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:carbonic anhydrase i deficiency
    n1=en:roberts syndrome | n2=en:carbonic anhydrase i deficiency | rel=r_associated | relid=0 | w=20
  961. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:cardio-facio-cutaneous syndrome
    n1=en:roberts syndrome | n2=en:cardio-facio-cutaneous syndrome | rel=r_associated | relid=0 | w=20
  962. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:cataplexia
    n1=en:roberts syndrome | n2=en:cataplexia | rel=r_associated | relid=0 | w=20
  963. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:cataplexis
    n1=en:roberts syndrome | n2=en:cataplexis | rel=r_associated | relid=0 | w=20
  964. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:CDA
    n1=en:roberts syndrome | n2=en:CDA | rel=r_associated | relid=0 | w=20
  965. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:cerebellar atrophy
    n1=en:roberts syndrome | n2=en:cerebellar atrophy | rel=r_associated | relid=0 | w=20
  966. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:cerebral gigantism
    n1=en:roberts syndrome | n2=en:cerebral gigantism | rel=r_associated | relid=0 | w=20
  967. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:cerebral tuberculosis
    n1=en:roberts syndrome | n2=en:cerebral tuberculosis | rel=r_associated | relid=0 | w=20
  968. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:cerebral ventriculomegaly
    n1=en:roberts syndrome | n2=en:cerebral ventriculomegaly | rel=r_associated | relid=0 | w=20
  969. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:child's sudden death
    n1=en:roberts syndrome | n2=en:child's sudden death | rel=r_associated | relid=0 | w=20
  970. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:chromosome 16p12.1 deletion syndrome
    n1=en:roberts syndrome | n2=en:chromosome 16p12.1 deletion syndrome | rel=r_associated | relid=0 | w=20
  971. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:classical maple syrup urine disease
    n1=en:roberts syndrome | n2=en:classical maple syrup urine disease | rel=r_associated | relid=0 | w=20
  972. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:cleft lip and palate
    n1=en:roberts syndrome | n2=en:cleft lip and palate | rel=r_associated | relid=0 | w=20
  973. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:coloboma and anal atresia syndrome
    n1=en:roberts syndrome | n2=en:coloboma and anal atresia syndrome | rel=r_associated | relid=0 | w=20
  974. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:cortical dysplasia-focal epilepsy syndrome
    n1=en:roberts syndrome | n2=en:cortical dysplasia-focal epilepsy syndrome | rel=r_associated | relid=0 | w=20
  975. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:cot death
    n1=en:roberts syndrome | n2=en:cot death | rel=r_associated | relid=0 | w=20
  976. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:craniostenosis
    n1=en:roberts syndrome | n2=en:craniostenosis | rel=r_associated | relid=0 | w=20
  977. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:crib death
    n1=en:roberts syndrome | n2=en:crib death | rel=r_associated | relid=0 | w=20
  978. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:cysticercosis
    n1=en:roberts syndrome | n2=en:cysticercosis | rel=r_associated | relid=0 | w=20
  979. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:cysticercus disease
    n1=en:roberts syndrome | n2=en:cysticercus disease | rel=r_associated | relid=0 | w=20
  980. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome
    n1=en:roberts syndrome | n2=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | rel=r_associated | relid=0 | w=20
  981. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Degos's syndrome
    n1=en:roberts syndrome | n2=en:Degos's syndrome | rel=r_associated | relid=0 | w=20
  982. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Dercum's disease
    n1=en:roberts syndrome | n2=en:Dercum's disease | rel=r_associated | relid=0 | w=20
  983. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Devergie's disease
    n1=en:roberts syndrome | n2=en:Devergie's disease | rel=r_associated | relid=0 | w=20
  984. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:disease aids
    n1=en:roberts syndrome | n2=en:disease aids | rel=r_associated | relid=0 | w=20
  985. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Diskinson's syndrome
    n1=en:roberts syndrome | n2=en:Diskinson's syndrome | rel=r_associated | relid=0 | w=20
  986. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Down syndrome
    n1=en:roberts syndrome | n2=en:Down syndrome | rel=r_associated | relid=0 | w=20
  987. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Duane's syndrome
    n1=en:roberts syndrome | n2=en:Duane's syndrome | rel=r_associated | relid=0 | w=20
  988. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:dumping stomach
    n1=en:roberts syndrome | n2=en:dumping stomach | rel=r_associated | relid=0 | w=20
  989. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:eiken type chondrodysplasia
    n1=en:roberts syndrome | n2=en:eiken type chondrodysplasia | rel=r_associated | relid=0 | w=20
  990. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:erythermalgia
    n1=en:roberts syndrome | n2=en:erythermalgia | rel=r_associated | relid=0 | w=20
  991. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:exomphalos
    n1=en:roberts syndrome | n2=en:exomphalos | rel=r_associated | relid=0 | w=20
  992. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:feeble-mindedness
    n1=en:roberts syndrome | n2=en:feeble-mindedness | rel=r_associated | relid=0 | w=20
  993. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:fish skin disease
    n1=en:roberts syndrome | n2=en:fish skin disease | rel=r_associated | relid=0 | w=20
  994. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Fox-Fordyce disease
    n1=en:roberts syndrome | n2=en:Fox-Fordyce disease | rel=r_associated | relid=0 | w=20
  995. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:FPLD
    n1=en:roberts syndrome | n2=en:FPLD | rel=r_associated | relid=0 | w=20
  996. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:fragile X syndrome
    n1=en:roberts syndrome | n2=en:fragile X syndrome | rel=r_associated | relid=0 | w=20
  997. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:gargoylism
    n1=en:roberts syndrome | n2=en:gargoylism | rel=r_associated | relid=0 | w=20
  998. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Gitelman syndrome
    n1=en:roberts syndrome | n2=en:Gitelman syndrome | rel=r_associated | relid=0 | w=20
  999. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:glutaric aciduria type 1
    n1=en:roberts syndrome | n2=en:glutaric aciduria type 1 | rel=r_associated | relid=0 | w=20
  1000. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:glutaric aciduria, type 1
    n1=en:roberts syndrome | n2=en:glutaric aciduria, type 1 | rel=r_associated | relid=0 | w=20
  1001. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Goltz syndrome
    n1=en:roberts syndrome | n2=en:Goltz syndrome | rel=r_associated | relid=0 | w=20
  1002. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Gray platelet syndrome
    n1=en:roberts syndrome | n2=en:Gray platelet syndrome | rel=r_associated | relid=0 | w=20
  1003. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Guillain-Barre syndrome
    n1=en:roberts syndrome | n2=en:Guillain-Barre syndrome | rel=r_associated | relid=0 | w=20
  1004. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Günther's disease
    n1=en:roberts syndrome | n2=en:Günther's disease | rel=r_associated | relid=0 | w=20
  1005. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:hand and foot deformity
    n1=en:roberts syndrome | n2=en:hand and foot deformity | rel=r_associated | relid=0 | w=20
  1006. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:hansenarium
    n1=en:roberts syndrome | n2=en:hansenarium | rel=r_associated | relid=0 | w=20
  1007. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Hebra's pityriasis
    n1=en:roberts syndrome | n2=en:Hebra's pityriasis | rel=r_associated | relid=0 | w=20
  1008. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:heterotaxy
    n1=en:roberts syndrome | n2=en:heterotaxy | rel=r_associated | relid=0 | w=20
  1009. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Hurler syndrome
    n1=en:roberts syndrome | n2=en:Hurler syndrome | rel=r_associated | relid=0 | w=20
  1010. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:hydrencephalus
    n1=en:roberts syndrome | n2=en:hydrencephalus | rel=r_associated | relid=0 | w=20
  1011. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:hypothalamic hamartoblastoma
    n1=en:roberts syndrome | n2=en:hypothalamic hamartoblastoma | rel=r_associated | relid=0 | w=20
  1012. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:hypoxaemia
    n1=en:roberts syndrome | n2=en:hypoxaemia | rel=r_associated | relid=0 | w=20
  1013. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:ichthyosis vera
    n1=en:roberts syndrome | n2=en:ichthyosis vera | rel=r_associated | relid=0 | w=20
  1014. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:immune deficiency syndrome
    n1=en:roberts syndrome | n2=en:immune deficiency syndrome | rel=r_associated | relid=0 | w=20
  1015. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:insulin receptor mutation - associated insulin resistance syndromes
    n1=en:roberts syndrome | n2=en:insulin receptor mutation - associated insulin resistance syndromes | rel=r_associated | relid=0 | w=20
  1016. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:juvenile cataract
    n1=en:roberts syndrome | n2=en:juvenile cataract | rel=r_associated | relid=0 | w=20
  1017. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Kawasaki disease
    n1=en:roberts syndrome | n2=en:Kawasaki disease | rel=r_associated | relid=0 | w=20
  1018. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Kawasaki's syndrome
    n1=en:roberts syndrome | n2=en:Kawasaki's syndrome | rel=r_associated | relid=0 | w=20
  1019. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:kenny-caffey syndrome type 2
    n1=en:roberts syndrome | n2=en:kenny-caffey syndrome type 2 | rel=r_associated | relid=0 | w=20
  1020. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Klinefelter syndrome
    n1=en:roberts syndrome | n2=en:Klinefelter syndrome | rel=r_associated | relid=0 | w=20
  1021. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Korsakoff syndrome
    n1=en:roberts syndrome | n2=en:Korsakoff syndrome | rel=r_associated | relid=0 | w=20
  1022. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:learning disability
    n1=en:roberts syndrome | n2=en:learning disability | rel=r_associated | relid=0 | w=20
  1023. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:leprosary
    n1=en:roberts syndrome | n2=en:leprosary | rel=r_associated | relid=0 | w=20
  1024. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Leriche syndrome
    n1=en:roberts syndrome | n2=en:Leriche syndrome | rel=r_associated | relid=0 | w=20
  1025. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:lethal neonatal rigidity and multifocal seizure syndrome
    n1=en:roberts syndrome | n2=en:lethal neonatal rigidity and multifocal seizure syndrome | rel=r_associated | relid=0 | w=20
  1026. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:leucinosis
    n1=en:roberts syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1027. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
    n1=en:roberts syndrome | n2=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
  1028. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:maple-tree syrup disease
    n1=en:roberts syndrome | n2=en:maple-tree syrup disease | rel=r_associated | relid=0 | w=20
  1029. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Marburg virus disease
    n1=en:roberts syndrome | n2=en:Marburg virus disease | rel=r_associated | relid=0 | w=20
  1030. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Marfan's disease
    n1=en:roberts syndrome | n2=en:Marfan's disease | rel=r_associated | relid=0 | w=20
  1031. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Marfan's syndrome
    n1=en:roberts syndrome | n2=en:Marfan's syndrome | rel=r_associated | relid=0 | w=20
  1032. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:maternal diabetes and deafness syndrome
    n1=en:roberts syndrome | n2=en:maternal diabetes and deafness syndrome | rel=r_associated | relid=0 | w=20
  1033. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:mental deficiency
    n1=en:roberts syndrome | n2=en:mental deficiency | rel=r_associated | relid=0 | w=20
  1034. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:mental handicap
    n1=en:roberts syndrome | n2=en:mental handicap | rel=r_associated | relid=0 | w=20
  1035. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:mental retardation, autosomal dominant 9
    n1=en:roberts syndrome | n2=en:mental retardation, autosomal dominant 9 | rel=r_associated | relid=0 | w=20
  1036. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:mental retardation, autosomal recessive 34
    n1=en:roberts syndrome | n2=en:mental retardation, autosomal recessive 34 | rel=r_associated | relid=0 | w=20
  1037. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:micrognathia
    n1=en:roberts syndrome | n2=en:micrognathia | rel=r_associated | relid=0 | w=20
  1038. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:mitochondrial dna depletion syndrome 12
    n1=en:roberts syndrome | n2=en:mitochondrial dna depletion syndrome 12 | rel=r_associated | relid=0 | w=20
  1039. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:morosis
    n1=en:roberts syndrome | n2=en:morosis | rel=r_associated | relid=0 | w=20
  1040. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:mucocutaneous lymph node syndrome
    n1=en:roberts syndrome | n2=en:mucocutaneous lymph node syndrome | rel=r_associated | relid=0 | w=20
  1041. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:mucolipidosis type iii gamma
    n1=en:roberts syndrome | n2=en:mucolipidosis type iii gamma | rel=r_associated | relid=0 | w=20
  1042. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:mullerian-renal-cervical spine syndrome
    n1=en:roberts syndrome | n2=en:mullerian-renal-cervical spine syndrome | rel=r_associated | relid=0 | w=20
  1043. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:multiple vascular disruption syndrome
    n1=en:roberts syndrome | n2=en:multiple vascular disruption syndrome | rel=r_associated | relid=0 | w=20
  1044. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:neurological cysticercosis
    n1=en:roberts syndrome | n2=en:neurological cysticercosis | rel=r_associated | relid=0 | w=20
  1045. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:oculorespiratory syndrome
    n1=en:roberts syndrome | n2=en:oculorespiratory syndrome | rel=r_associated | relid=0 | w=20
  1046. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:odontogenesis imperfecta
    n1=en:roberts syndrome | n2=en:odontogenesis imperfecta | rel=r_associated | relid=0 | w=20
  1047. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:oligergasia
    n1=en:roberts syndrome | n2=en:oligergasia | rel=r_associated | relid=0 | w=20
  1048. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:ophthalmoneuritis
    n1=en:roberts syndrome | n2=en:ophthalmoneuritis | rel=r_associated | relid=0 | w=20
  1049. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:osteopoecilia
    n1=en:roberts syndrome | n2=en:osteopoecilia | rel=r_associated | relid=0 | w=20
  1050. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Pick's disease
    n1=en:roberts syndrome | n2=en:Pick's disease | rel=r_associated | relid=0 | w=20
  1051. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:plasma kallikrein deficiency
    n1=en:roberts syndrome | n2=en:plasma kallikrein deficiency | rel=r_associated | relid=0 | w=20
  1052. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Plummer-Vinson syndrome
    n1=en:roberts syndrome | n2=en:Plummer-Vinson syndrome | rel=r_associated | relid=0 | w=20
  1053. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Prader-Willi syndrome
    n1=en:roberts syndrome | n2=en:Prader-Willi syndrome | rel=r_associated | relid=0 | w=20
  1054. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:proctatresia
    n1=en:roberts syndrome | n2=en:proctatresia | rel=r_associated | relid=0 | w=20
  1055. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:proptosis
    n1=en:roberts syndrome | n2=en:proptosis | rel=r_associated | relid=0 | w=20
  1056. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:protopsis
    n1=en:roberts syndrome | n2=en:protopsis | rel=r_associated | relid=0 | w=20
  1057. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:pulmonary shunting
    n1=en:roberts syndrome | n2=en:pulmonary shunting | rel=r_associated | relid=0 | w=20
  1058. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:respiratory distress
    n1=en:roberts syndrome | n2=en:respiratory distress | rel=r_associated | relid=0 | w=20
  1059. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:retardation
    n1=en:roberts syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
  1060. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:schock lung
    n1=en:roberts syndrome | n2=en:schock lung | rel=r_associated | relid=0 | w=20
  1061. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Seitelberger's disease
    n1=en:roberts syndrome | n2=en:Seitelberger's disease | rel=r_associated | relid=0 | w=20
  1062. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Seitelberger's neuroaxonal dystrophy
    n1=en:roberts syndrome | n2=en:Seitelberger's neuroaxonal dystrophy | rel=r_associated | relid=0 | w=20
  1063. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:SIDS
    n1=en:roberts syndrome | n2=en:SIDS | rel=r_associated | relid=0 | w=20
  1064. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:sids
    n1=en:roberts syndrome | n2=en:sids | rel=r_associated | relid=0 | w=20
  1065. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:single central incisor syndrome
    n1=en:roberts syndrome | n2=en:single central incisor syndrome | rel=r_associated | relid=0 | w=20
  1066. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:situs inversus
    n1=en:roberts syndrome | n2=en:situs inversus | rel=r_associated | relid=0 | w=20
  1067. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:situs inversus viscerum
    n1=en:roberts syndrome | n2=en:situs inversus viscerum | rel=r_associated | relid=0 | w=20
  1068. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:situs mutatus
    n1=en:roberts syndrome | n2=en:situs mutatus | rel=r_associated | relid=0 | w=20
  1069. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Soto's syndrome
    n1=en:roberts syndrome | n2=en:Soto's syndrome | rel=r_associated | relid=0 | w=20
  1070. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Sotos' syndrome
    n1=en:roberts syndrome | n2=en:Sotos' syndrome | rel=r_associated | relid=0 | w=20
  1071. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:sotos' syndrome
    n1=en:roberts syndrome | n2=en:sotos' syndrome | rel=r_associated | relid=0 | w=20
  1072. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Stargardt disease
    n1=en:roberts syndrome | n2=en:Stargardt disease | rel=r_associated | relid=0 | w=20
  1073. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Stokes-Adams syndrome
    n1=en:roberts syndrome | n2=en:Stokes-Adams syndrome | rel=r_associated | relid=0 | w=20
  1074. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Tay-Sachs disease
    n1=en:roberts syndrome | n2=en:Tay-Sachs disease | rel=r_associated | relid=0 | w=20
  1075. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:telecanthus
    n1=en:roberts syndrome | n2=en:telecanthus | rel=r_associated | relid=0 | w=20
  1076. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:thiamin-responsive maple syrup urine disease
    n1=en:roberts syndrome | n2=en:thiamin-responsive maple syrup urine disease | rel=r_associated | relid=0 | w=20
  1077. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:tissue kallikrein deficiency
    n1=en:roberts syndrome | n2=en:tissue kallikrein deficiency | rel=r_associated | relid=0 | w=20
  1078. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Townes-Brocks syndrome
    n1=en:roberts syndrome | n2=en:Townes-Brocks syndrome | rel=r_associated | relid=0 | w=20
  1079. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Toxic Shock Syndrome
    n1=en:roberts syndrome | n2=en:Toxic Shock Syndrome | rel=r_associated | relid=0 | w=20
  1080. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:trichorhinophalangeal syndrome type II
    n1=en:roberts syndrome | n2=en:trichorhinophalangeal syndrome type II | rel=r_associated | relid=0 | w=20
  1081. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:triple a syndrome
    n1=en:roberts syndrome | n2=en:triple a syndrome | rel=r_associated | relid=0 | w=20
  1082. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Triple a syndrome
    n1=en:roberts syndrome | n2=en:Triple a syndrome | rel=r_associated | relid=0 | w=20
  1083. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:tuberculosis of meninges (cerebral)(spinal)
    n1=en:roberts syndrome | n2=en:tuberculosis of meninges (cerebral)(spinal) | rel=r_associated | relid=0 | w=20
  1084. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:tuberculosis, meningeal
    n1=en:roberts syndrome | n2=en:tuberculosis, meningeal | rel=r_associated | relid=0 | w=20
  1085. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:tuberculous hypertrophic pachymeningitides
    n1=en:roberts syndrome | n2=en:tuberculous hypertrophic pachymeningitides | rel=r_associated | relid=0 | w=20
  1086. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:tuberculous leptomeningitis
    n1=en:roberts syndrome | n2=en:tuberculous leptomeningitis | rel=r_associated | relid=0 | w=20
  1087. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:tuberculous meningitis
    n1=en:roberts syndrome | n2=en:tuberculous meningitis | rel=r_associated | relid=0 | w=20
  1088. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:ventriculomeglia
    n1=en:roberts syndrome | n2=en:ventriculomeglia | rel=r_associated | relid=0 | w=20
  1089. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Waterhouse-Friderichsen syndrome
    n1=en:roberts syndrome | n2=en:Waterhouse-Friderichsen syndrome | rel=r_associated | relid=0 | w=20
  1090. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Whipple disease
    n1=en:roberts syndrome | n2=en:Whipple disease | rel=r_associated | relid=0 | w=20
  1091. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Williams syndrome
    n1=en:roberts syndrome | n2=en:Williams syndrome | rel=r_associated | relid=0 | w=20
  1092. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:wilms tumor 1 gene syndromes
    n1=en:roberts syndrome | n2=en:wilms tumor 1 gene syndromes | rel=r_associated | relid=0 | w=20
  1093. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:with growth retardation
    n1=en:roberts syndrome | n2=en:with growth retardation | rel=r_associated | relid=0 | w=20
  1094. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:xerophtalmy
    n1=en:roberts syndrome | n2=en:xerophtalmy | rel=r_associated | relid=0 | w=20
  1095. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:yellow nail
    n1=en:roberts syndrome | n2=en:yellow nail | rel=r_associated | relid=0 | w=20
  1096. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> en:Zellweger syndrome
    n1=en:roberts syndrome | n2=en:Zellweger syndrome | rel=r_associated | relid=0 | w=20
  1097. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> érythermalgie
    n1=en:roberts syndrome | n2=érythermalgie | rel=r_associated | relid=0 | w=20
  1098. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> erythromelalgia
    n1=en:roberts syndrome | n2=erythromelalgia | rel=r_associated | relid=0 | w=20
  1099. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> érythromélalgie
    n1=en:roberts syndrome | n2=érythromélalgie | rel=r_associated | relid=0 | w=20
  1100. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> examen non précisé, méningite tuberculeuse
    n1=en:roberts syndrome | n2=examen non précisé, méningite tuberculeuse | rel=r_associated | relid=0 | w=20
  1101. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> exophtalmie
    n1=en:roberts syndrome | n2=exophtalmie | rel=r_associated | relid=0 | w=20
  1102. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> exophthalmie
    n1=en:roberts syndrome | n2=exophthalmie | rel=r_associated | relid=0 | w=20
  1103. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> faciès anormal, retard de croissance et retard mental
    n1=en:roberts syndrome | n2=faciès anormal, retard de croissance et retard mental | rel=r_associated | relid=0 | w=20
  1104. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> fibromyalgie
    n1=en:roberts syndrome | n2=fibromyalgie | rel=r_associated | relid=0 | w=20
  1105. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> fragilité osseuse avec craniosynostose, exophtalmie, hydrocéphalie et faciès caractéristique
    n1=en:roberts syndrome | n2=fragilité osseuse avec craniosynostose, exophtalmie, hydrocéphalie et faciès caractéristique | rel=r_associated | relid=0 | w=20
  1106. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> gigantisme cérébral
    n1=en:roberts syndrome | n2=gigantisme cérébral | rel=r_associated | relid=0 | w=20
  1107. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> glycogénose
    n1=en:roberts syndrome | n2=glycogénose | rel=r_associated | relid=0 | w=20
  1108. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Goltz
    n1=en:roberts syndrome | n2=Goltz | rel=r_associated | relid=0 | w=20
  1109. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale
    n1=en:roberts syndrome | n2=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | rel=r_associated | relid=0 | w=20
  1110. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hémicéphalie
    n1=en:roberts syndrome | n2=hémicéphalie | rel=r_associated | relid=0 | w=20
  1111. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hérédité autosomale récessive
    n1=en:roberts syndrome | n2=hérédité autosomale récessive | rel=r_associated | relid=0 | w=20
  1112. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle
    n1=en:roberts syndrome | n2=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | rel=r_associated | relid=0 | w=20
  1113. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hétérotaxie
    n1=en:roberts syndrome | n2=hétérotaxie | rel=r_associated | relid=0 | w=20
  1114. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> holoprosencéphalie
    n1=en:roberts syndrome | n2=holoprosencéphalie | rel=r_associated | relid=0 | w=20
  1115. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> holoprosencéphalie de type 2
    n1=en:roberts syndrome | n2=holoprosencéphalie de type 2 | rel=r_associated | relid=0 | w=20
  1116. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> holoprosencéphalie de type 3
    n1=en:roberts syndrome | n2=holoprosencéphalie de type 3 | rel=r_associated | relid=0 | w=20
  1117. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> holoprosencéphalie de type 4
    n1=en:roberts syndrome | n2=holoprosencéphalie de type 4 | rel=r_associated | relid=0 | w=20
  1118. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> holoprosencéphalie familiale alobaire de type 1
    n1=en:roberts syndrome | n2=holoprosencéphalie familiale alobaire de type 1 | rel=r_associated | relid=0 | w=20
  1119. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hydramnios
    n1=en:roberts syndrome | n2=hydramnios | rel=r_associated | relid=0 | w=20
  1120. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hydroa vacciniforme
    n1=en:roberts syndrome | n2=hydroa vacciniforme | rel=r_associated | relid=0 | w=20
  1121. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hydroa vacciniforme de Bazin
    n1=en:roberts syndrome | n2=hydroa vacciniforme de Bazin | rel=r_associated | relid=0 | w=20
  1122. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hydrocéphalie
    n1=en:roberts syndrome | n2=hydrocéphalie | rel=r_associated | relid=0 | w=20
  1123. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hydrops foetoplacentaire
    n1=en:roberts syndrome | n2=hydrops foetoplacentaire | rel=r_associated | relid=0 | w=20
  1124. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hypertélorisme
    n1=en:roberts syndrome | n2=hypertélorisme | rel=r_associated | relid=0 | w=20
  1125. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hypertélorisme-microtie-fente faciale
    n1=en:roberts syndrome | n2=hypertélorisme-microtie-fente faciale | rel=r_associated | relid=0 | w=20
  1126. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hypertélorisme, hypospadias, polysyndactylie (syndrome)
    n1=en:roberts syndrome | n2=hypertélorisme, hypospadias, polysyndactylie (syndrome) | rel=r_associated | relid=0 | w=20
  1127. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hypoplasie dermique en aires
    n1=en:roberts syndrome | n2=hypoplasie dermique en aires | rel=r_associated | relid=0 | w=20
  1128. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hypoplasie dermique focale
    n1=en:roberts syndrome | n2=hypoplasie dermique focale | rel=r_associated | relid=0 | w=20
  1129. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> hypoxémie
    n1=en:roberts syndrome | n2=hypoxémie | rel=r_associated | relid=0 | w=20
  1130. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ichthyose
    n1=en:roberts syndrome | n2=ichthyose | rel=r_associated | relid=0 | w=20
  1131. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ichtyose
    n1=en:roberts syndrome | n2=ichtyose | rel=r_associated | relid=0 | w=20
  1132. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ichtyose folliculaire, atrichie et photophobie
    n1=en:roberts syndrome | n2=ichtyose folliculaire, atrichie et photophobie | rel=r_associated | relid=0 | w=20
  1133. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ichtyose, affection neurologique spastique, et oligophrénie
    n1=en:roberts syndrome | n2=ichtyose, affection neurologique spastique, et oligophrénie | rel=r_associated | relid=0 | w=20
  1134. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ictère nucléaire
    n1=en:roberts syndrome | n2=ictère nucléaire | rel=r_associated | relid=0 | w=20
  1135. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> idiotie spastique amaurotique axonale
    n1=en:roberts syndrome | n2=idiotie spastique amaurotique axonale | rel=r_associated | relid=0 | w=20
  1136. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> imperforation anale
    n1=en:roberts syndrome | n2=imperforation anale | rel=r_associated | relid=0 | w=20
  1137. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> imperforation de l'anus
    n1=en:roberts syndrome | n2=imperforation de l'anus | rel=r_associated | relid=0 | w=20
  1138. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> inflammation musculaire
    n1=en:roberts syndrome | n2=inflammation musculaire | rel=r_associated | relid=0 | w=20
  1139. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> insensibilité congénitale à la douleur de type III
    n1=en:roberts syndrome | n2=insensibilité congénitale à la douleur de type III | rel=r_associated | relid=0 | w=20
  1140. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> insuffisance pulmonaire post-traumatique
    n1=en:roberts syndrome | n2=insuffisance pulmonaire post-traumatique | rel=r_associated | relid=0 | w=20
  1141. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> intolérance au fructose
    n1=en:roberts syndrome | n2=intolérance au fructose | rel=r_associated | relid=0 | w=20
  1142. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Jacobsen (syndrome de)
    n1=en:roberts syndrome | n2=Jacobsen (syndrome de) | rel=r_associated | relid=0 | w=20
  1143. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Kawasaki (maladie de)
    n1=en:roberts syndrome | n2=Kawasaki (maladie de) | rel=r_associated | relid=0 | w=20
  1144. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> lèpre
    n1=en:roberts syndrome | n2=lèpre | rel=r_associated | relid=0 | w=20
  1145. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> léproserie
    n1=en:roberts syndrome | n2=léproserie | rel=r_associated | relid=0 | w=20
  1146. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> leprosy
    n1=en:roberts syndrome | n2=leprosy | rel=r_associated | relid=0 | w=20
  1147. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> leptoméningite tuberculeuse
    n1=en:roberts syndrome | n2=leptoméningite tuberculeuse | rel=r_associated | relid=0 | w=20
  1148. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> leucinose
    n1=en:roberts syndrome | n2=leucinose | rel=r_associated | relid=0 | w=20
  1149. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> lévocardie
    n1=en:roberts syndrome | n2=lévocardie | rel=r_associated | relid=0 | w=20
  1150. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> lichen ruber acuminatus
    n1=en:roberts syndrome | n2=lichen ruber acuminatus | rel=r_associated | relid=0 | w=20
  1151. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> lipodystrophie partielle familiale
    n1=en:roberts syndrome | n2=lipodystrophie partielle familiale | rel=r_associated | relid=0 | w=20
  1152. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> lissencéphalie
    n1=en:roberts syndrome | n2=lissencéphalie | rel=r_associated | relid=0 | w=20
  1153. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie à virus de Marburg
    n1=en:roberts syndrome | n2=maladie à virus de Marburg | rel=r_associated | relid=0 | w=20
  1154. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de Caffey
    n1=en:roberts syndrome | n2=maladie de Caffey | rel=r_associated | relid=0 | w=20
  1155. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de Dercum
    n1=en:roberts syndrome | n2=maladie de Dercum | rel=r_associated | relid=0 | w=20
  1156. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de dercum
    n1=en:roberts syndrome | n2=maladie de dercum | rel=r_associated | relid=0 | w=20
  1157. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de dubin-johnson
    n1=en:roberts syndrome | n2=maladie de dubin-johnson | rel=r_associated | relid=0 | w=20
  1158. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de hurler
    n1=en:roberts syndrome | n2=maladie de hurler | rel=r_associated | relid=0 | w=20
  1159. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de Hurler
    n1=en:roberts syndrome | n2=maladie de Hurler | rel=r_associated | relid=0 | w=20
  1160. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de Kawasaki
    n1=en:roberts syndrome | n2=maladie de Kawasaki | rel=r_associated | relid=0 | w=20
  1161. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de marfan
    n1=en:roberts syndrome | n2=maladie de marfan | rel=r_associated | relid=0 | w=20
  1162. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de Perthes
    n1=en:roberts syndrome | n2=maladie de Perthes | rel=r_associated | relid=0 | w=20
  1163. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de Roger
    n1=en:roberts syndrome | n2=maladie de Roger | rel=r_associated | relid=0 | w=20
  1164. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de Seitelberger
    n1=en:roberts syndrome | n2=maladie de Seitelberger | rel=r_associated | relid=0 | w=20
  1165. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de seitelberger
    n1=en:roberts syndrome | n2=maladie de seitelberger | rel=r_associated | relid=0 | w=20
  1166. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de tay-sachs
    n1=en:roberts syndrome | n2=maladie de tay-sachs | rel=r_associated | relid=0 | w=20
  1167. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de Tay-sachs
    n1=en:roberts syndrome | n2=maladie de Tay-sachs | rel=r_associated | relid=0 | w=20
  1168. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Maladie de Tay-Sachs
    n1=en:roberts syndrome | n2=Maladie de Tay-Sachs | rel=r_associated | relid=0 | w=20
  1169. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de Tay-Sachs
    n1=en:roberts syndrome | n2=maladie de Tay-Sachs | rel=r_associated | relid=0 | w=20
  1170. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de Whipple
    n1=en:roberts syndrome | n2=maladie de Whipple | rel=r_associated | relid=0 | w=20
  1171. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie de whipple
    n1=en:roberts syndrome | n2=maladie de whipple | rel=r_associated | relid=0 | w=20
  1172. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie des épiphyses ponctuées
    n1=en:roberts syndrome | n2=maladie des épiphyses ponctuées | rel=r_associated | relid=0 | w=20
  1173. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie des urines à l'odeur de sirop d'érable
    n1=en:roberts syndrome | n2=maladie des urines à l'odeur de sirop d'érable | rel=r_associated | relid=0 | w=20
  1174. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie des urines avec odeur de sirop erable
    n1=en:roberts syndrome | n2=maladie des urines avec odeur de sirop erable | rel=r_associated | relid=0 | w=20
  1175. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie du cri du chat
    n1=en:roberts syndrome | n2=maladie du cri du chat | rel=r_associated | relid=0 | w=20
  1176. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie du sirop d'érable
    n1=en:roberts syndrome | n2=maladie du sirop d'érable | rel=r_associated | relid=0 | w=20
  1177. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladie lysosomique de surcharge
    n1=en:roberts syndrome | n2=maladie lysosomique de surcharge | rel=r_associated | relid=0 | w=20
  1178. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> maladies des bandes amniotiques
    n1=en:roberts syndrome | n2=maladies des bandes amniotiques | rel=r_associated | relid=0 | w=20
  1179. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> malformation d'Arnold-Chiari
    n1=en:roberts syndrome | n2=malformation d'Arnold-Chiari | rel=r_associated | relid=0 | w=20
  1180. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> malformation d'arnold-chiari
    n1=en:roberts syndrome | n2=malformation d'arnold-chiari | rel=r_associated | relid=0 | w=20
  1181. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Malformation d'Arnold-Chiari
    n1=en:roberts syndrome | n2=Malformation d'Arnold-Chiari | rel=r_associated | relid=0 | w=20
  1182. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Marfan (maladie de)
    n1=en:roberts syndrome | n2=Marfan (maladie de) | rel=r_associated | relid=0 | w=20
  1183. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> méningite tuberculeuse
    n1=en:roberts syndrome | n2=méningite tuberculeuse | rel=r_associated | relid=0 | w=20
  1184. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> méningite tuberculeuse examen non précisé
    n1=en:roberts syndrome | n2=méningite tuberculeuse examen non précisé | rel=r_associated | relid=0 | w=20
  1185. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> mésentérique supérieure (syndrome de l'artère)
    n1=en:roberts syndrome | n2=mésentérique supérieure (syndrome de l'artère) | rel=r_associated | relid=0 | w=20
  1186. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> microdélétion 5q35
    n1=en:roberts syndrome | n2=microdélétion 5q35 | rel=r_associated | relid=0 | w=20
  1187. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> micrognathie
    n1=en:roberts syndrome | n2=micrognathie | rel=r_associated | relid=0 | w=20
  1188. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> micrognathisme
    n1=en:roberts syndrome | n2=micrognathisme | rel=r_associated | relid=0 | w=20
  1189. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> mort subite du nourrisson
    n1=en:roberts syndrome | n2=mort subite du nourrisson | rel=r_associated | relid=0 | w=20
  1190. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> myocardiopathie de tako-tsubo
    n1=en:roberts syndrome | n2=myocardiopathie de tako-tsubo | rel=r_associated | relid=0 | w=20
  1191. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> myokymie
    n1=en:roberts syndrome | n2=myokymie | rel=r_associated | relid=0 | w=20
  1192. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> myosite
    n1=en:roberts syndrome | n2=myosite | rel=r_associated | relid=0 | w=20
  1193. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> myosites
    n1=en:roberts syndrome | n2=myosites | rel=r_associated | relid=0 | w=20
  1194. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> nanisme, retard mental, anomalies oculaires
    n1=en:roberts syndrome | n2=nanisme, retard mental, anomalies oculaires | rel=r_associated | relid=0 | w=20
  1195. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> néphrocalcinose
    n1=en:roberts syndrome | n2=néphrocalcinose | rel=r_associated | relid=0 | w=20
  1196. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> neuro-acanthocytose
    n1=en:roberts syndrome | n2=neuro-acanthocytose | rel=r_associated | relid=0 | w=20
  1197. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> neurocysticercose
    n1=en:roberts syndrome | n2=neurocysticercose | rel=r_associated | relid=0 | w=20
  1198. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> neuropathie optique
    n1=en:roberts syndrome | n2=neuropathie optique | rel=r_associated | relid=0 | w=20
  1199. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> nevrilème
    n1=en:roberts syndrome | n2=nevrilème | rel=r_associated | relid=0 | w=20
  1200. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> névrite optique
    n1=en:roberts syndrome | n2=névrite optique | rel=r_associated | relid=0 | w=20
  1201. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> noma
    n1=en:roberts syndrome | n2=noma | rel=r_associated | relid=0 | w=20
  1202. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> odontogénèse imparfaite
    n1=en:roberts syndrome | n2=odontogénèse imparfaite | rel=r_associated | relid=0 | w=20
  1203. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> oedème du poumon non cardiogénique
    n1=en:roberts syndrome | n2=oedème du poumon non cardiogénique | rel=r_associated | relid=0 | w=20
  1204. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> oedème pulmonaire non cardiogénique
    n1=en:roberts syndrome | n2=oedème pulmonaire non cardiogénique | rel=r_associated | relid=0 | w=20
  1205. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> oligophrénie
    n1=en:roberts syndrome | n2=oligophrénie | rel=r_associated | relid=0 | w=20
  1206. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ongles jaunes (syndrome des)
    n1=en:roberts syndrome | n2=ongles jaunes (syndrome des) | rel=r_associated | relid=0 | w=20
  1207. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> onycho-ostéodysostose
    n1=en:roberts syndrome | n2=onycho-ostéodysostose | rel=r_associated | relid=0 | w=20
  1208. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> onycho-patellaire (syndrome)
    n1=en:roberts syndrome | n2=onycho-patellaire (syndrome) | rel=r_associated | relid=0 | w=20
  1209. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ophtalmorhino-stomatoxérose
    n1=en:roberts syndrome | n2=ophtalmorhino-stomatoxérose | rel=r_associated | relid=0 | w=20
  1210. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ostéochondrodysplasie
    n1=en:roberts syndrome | n2=ostéochondrodysplasie | rel=r_associated | relid=0 | w=20
  1211. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ostéochondrodysplasies
    n1=en:roberts syndrome | n2=ostéochondrodysplasies | rel=r_associated | relid=0 | w=20
  1212. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ostéopétrose avec acidose rénale tubulaire
    n1=en:roberts syndrome | n2=ostéopétrose avec acidose rénale tubulaire | rel=r_associated | relid=0 | w=20
  1213. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ostéopoecilie
    n1=en:roberts syndrome | n2=ostéopoecilie | rel=r_associated | relid=0 | w=20
  1214. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> pachyméningite hypertrophique tuberculeuse
    n1=en:roberts syndrome | n2=pachyméningite hypertrophique tuberculeuse | rel=r_associated | relid=0 | w=20
  1215. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> pachyonychie congénitale de Jadassohn-Lewandowsky
    n1=en:roberts syndrome | n2=pachyonychie congénitale de Jadassohn-Lewandowsky | rel=r_associated | relid=0 | w=20
  1216. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> panencéphalite subaiguë sclérosante
    n1=en:roberts syndrome | n2=panencéphalite subaiguë sclérosante | rel=r_associated | relid=0 | w=20
  1217. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> panuvéite
    n1=en:roberts syndrome | n2=panuvéite | rel=r_associated | relid=0 | w=20
  1218. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> papulose atrophiante maligne de Degos
    n1=en:roberts syndrome | n2=papulose atrophiante maligne de Degos | rel=r_associated | relid=0 | w=20
  1219. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> paragonimiase
    n1=en:roberts syndrome | n2=paragonimiase | rel=r_associated | relid=0 | w=20
  1220. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> paragonimose
    n1=en:roberts syndrome | n2=paragonimose | rel=r_associated | relid=0 | w=20
  1221. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> paralysie périodique familiale
    n1=en:roberts syndrome | n2=paralysie périodique familiale | rel=r_associated | relid=0 | w=20
  1222. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> paralysie supranucléaire progressive
    n1=en:roberts syndrome | n2=paralysie supranucléaire progressive | rel=r_associated | relid=0 | w=20
  1223. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> pemphigoïde bénigne des muqueuses
    n1=en:roberts syndrome | n2=pemphigoïde bénigne des muqueuses | rel=r_associated | relid=0 | w=20
  1224. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> pemphigus bénin des muqueuses
    n1=en:roberts syndrome | n2=pemphigus bénin des muqueuses | rel=r_associated | relid=0 | w=20
  1225. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> peste
    n1=en:roberts syndrome | n2=peste | rel=r_associated | relid=0 | w=20
  1226. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> peste noire
    n1=en:roberts syndrome | n2=peste noire | rel=r_associated | relid=0 | w=20
  1227. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> phacomatose congenitale
    n1=en:roberts syndrome | n2=phacomatose congenitale | rel=r_associated | relid=0 | w=20
  1228. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> piébaldisme
    n1=en:roberts syndrome | n2=piébaldisme | rel=r_associated | relid=0 | w=20
  1229. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> piebaldisme
    n1=en:roberts syndrome | n2=piebaldisme | rel=r_associated | relid=0 | w=20
  1230. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> pityriasis rubra pilaire
    n1=en:roberts syndrome | n2=pityriasis rubra pilaire | rel=r_associated | relid=0 | w=20
  1231. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Pityriasis rubra pilaire
    n1=en:roberts syndrome | n2=Pityriasis rubra pilaire | rel=r_associated | relid=0 | w=20
  1232. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Plummer-Vinson (syndrome de)
    n1=en:roberts syndrome | n2=Plummer-Vinson (syndrome de) | rel=r_associated | relid=0 | w=20
  1233. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> polyhydramnios
    n1=en:roberts syndrome | n2=polyhydramnios | rel=r_associated | relid=0 | w=20
  1234. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> porphyrie (anesthésie chez un patient atteint de)
    n1=en:roberts syndrome | n2=porphyrie (anesthésie chez un patient atteint de) | rel=r_associated | relid=0 | w=20
  1235. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> porphyrie cutanée tardive
    n1=en:roberts syndrome | n2=porphyrie cutanée tardive | rel=r_associated | relid=0 | w=20
  1236. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> porphyrie érythropoïétique
    n1=en:roberts syndrome | n2=porphyrie érythropoïétique | rel=r_associated | relid=0 | w=20
  1237. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> poumon de choc
    n1=en:roberts syndrome | n2=poumon de choc | rel=r_associated | relid=0 | w=20
  1238. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> poumon de choc traumatique
    n1=en:roberts syndrome | n2=poumon de choc traumatique | rel=r_associated | relid=0 | w=20
  1239. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> poumon du vietnam
    n1=en:roberts syndrome | n2=poumon du vietnam | rel=r_associated | relid=0 | w=20
  1240. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> présentation sacro-iliaque droite antérieure
    n1=en:roberts syndrome | n2=présentation sacro-iliaque droite antérieure | rel=r_associated | relid=0 | w=20
  1241. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> progeria
    n1=en:roberts syndrome | n2=progeria | rel=r_associated | relid=0 | w=20
  1242. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> progéria
    n1=en:roberts syndrome | n2=progéria | rel=r_associated | relid=0 | w=20
  1243. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> proptose
    n1=en:roberts syndrome | n2=proptose | rel=r_associated | relid=0 | w=20
  1244. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> protéinose alvéolaire
    n1=en:roberts syndrome | n2=protéinose alvéolaire | rel=r_associated | relid=0 | w=20
  1245. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> protéinose alvéolaire pulmonaire
    n1=en:roberts syndrome | n2=protéinose alvéolaire pulmonaire | rel=r_associated | relid=0 | w=20
  1246. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> protoproporphyrie érythropoïétique
    n1=en:roberts syndrome | n2=protoproporphyrie érythropoïétique | rel=r_associated | relid=0 | w=20
  1247. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> psychose de Korsakoff
    n1=en:roberts syndrome | n2=psychose de Korsakoff | rel=r_associated | relid=0 | w=20
  1248. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> psychose de korsakoff
    n1=en:roberts syndrome | n2=psychose de korsakoff | rel=r_associated | relid=0 | w=20
  1249. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> queue de cheval (syndrome de la)
    n1=en:roberts syndrome | n2=queue de cheval (syndrome de la) | rel=r_associated | relid=0 | w=20
  1250. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> red man syndrome
    n1=en:roberts syndrome | n2=red man syndrome | rel=r_associated | relid=0 | w=20
  1251. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> retard mental
    n1=en:roberts syndrome | n2=retard mental | rel=r_associated | relid=0 | w=20
  1252. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Retard mental
    n1=en:roberts syndrome | n2=Retard mental | rel=r_associated | relid=0 | w=20
  1253. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> retard mental, retard de croissance, surdité, microgénitalisme lié au sexe
    n1=en:roberts syndrome | n2=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | rel=r_associated | relid=0 | w=20
  1254. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> retardation mentale
    n1=en:roberts syndrome | n2=retardation mentale | rel=r_associated | relid=0 | w=20
  1255. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> S.I.D.A.
    n1=en:roberts syndrome | n2=S.I.D.A. | rel=r_associated | relid=0 | w=20
  1256. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Sars
    n1=en:roberts syndrome | n2=Sars | rel=r_associated | relid=0 | w=20
  1257. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> scléromyxoedème d'Arndt-Gottron
    n1=en:roberts syndrome | n2=scléromyxoedème d'Arndt-Gottron | rel=r_associated | relid=0 | w=20
  1258. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Seitelberger
    n1=en:roberts syndrome | n2=Seitelberger | rel=r_associated | relid=0 | w=20
  1259. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Seitelberger (maladie de)
    n1=en:roberts syndrome | n2=Seitelberger (maladie de) | rel=r_associated | relid=0 | w=20
  1260. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> septo-optic dysplasia
    n1=en:roberts syndrome | n2=septo-optic dysplasia | rel=r_associated | relid=0 | w=20
  1261. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> sicca syndrome
    n1=en:roberts syndrome | n2=sicca syndrome | rel=r_associated | relid=0 | w=20
  1262. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> SIDA
    n1=en:roberts syndrome | n2=SIDA | rel=r_associated | relid=0 | w=20
  1263. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Silver-Russell (syndrome de)
    n1=en:roberts syndrome | n2=Silver-Russell (syndrome de) | rel=r_associated | relid=0 | w=20
  1264. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> sirop d'érable (urine à odeur de)
    n1=en:roberts syndrome | n2=sirop d'érable (urine à odeur de) | rel=r_associated | relid=0 | w=20
  1265. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> situs inversus
    n1=en:roberts syndrome | n2=situs inversus | rel=r_associated | relid=0 | w=20
  1266. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Sotos (syndrome de)
    n1=en:roberts syndrome | n2=Sotos (syndrome de) | rel=r_associated | relid=0 | w=20
  1267. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome adéno-cutanéo-muqueux
    n1=en:roberts syndrome | n2=syndrome adéno-cutanéo-muqueux | rel=r_associated | relid=0 | w=20
  1268. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome adénocutanéomuqueux
    n1=en:roberts syndrome | n2=syndrome adénocutanéomuqueux | rel=r_associated | relid=0 | w=20
  1269. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome cérébro-oculo-faciosquelettique
    n1=en:roberts syndrome | n2=syndrome cérébro-oculo-faciosquelettique | rel=r_associated | relid=0 | w=20
  1270. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'Adair-Dighton
    n1=en:roberts syndrome | n2=syndrome d'Adair-Dighton | rel=r_associated | relid=0 | w=20
  1271. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'Alagille
    n1=en:roberts syndrome | n2=syndrome d'Alagille | rel=r_associated | relid=0 | w=20
  1272. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'Alice au pays des merveilles
    n1=en:roberts syndrome | n2=syndrome d'Alice au pays des merveilles | rel=r_associated | relid=0 | w=20
  1273. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'Alport
    n1=en:roberts syndrome | n2=syndrome d'Alport | rel=r_associated | relid=0 | w=20
  1274. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'alport
    n1=en:roberts syndrome | n2=syndrome d'alport | rel=r_associated | relid=0 | w=20
  1275. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'angelman
    n1=en:roberts syndrome | n2=syndrome d'angelman | rel=r_associated | relid=0 | w=20
  1276. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'Angelman
    n1=en:roberts syndrome | n2=syndrome d'Angelman | rel=r_associated | relid=0 | w=20
  1277. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Syndrome d'Angelman
    n1=en:roberts syndrome | n2=Syndrome d'Angelman | rel=r_associated | relid=0 | w=20
  1278. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'immunodéficience acquise
    n1=en:roberts syndrome | n2=syndrome d'immunodéficience acquise | rel=r_associated | relid=0 | w=20
  1279. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de bile épaisse
    n1=en:roberts syndrome | n2=syndrome de bile épaisse | rel=r_associated | relid=0 | w=20
  1280. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de bride amniotique
    n1=en:roberts syndrome | n2=syndrome de bride amniotique | rel=r_associated | relid=0 | w=20
  1281. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de chasse
    n1=en:roberts syndrome | n2=syndrome de chasse | rel=r_associated | relid=0 | w=20
  1282. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de détresse respiratoire
    n1=en:roberts syndrome | n2=syndrome de détresse respiratoire | rel=r_associated | relid=0 | w=20
  1283. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de détresse respiratoire aiguë
    n1=en:roberts syndrome | n2=syndrome de détresse respiratoire aiguë | rel=r_associated | relid=0 | w=20
  1284. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de détresse respiratoire aigüe
    n1=en:roberts syndrome | n2=syndrome de détresse respiratoire aigüe | rel=r_associated | relid=0 | w=20
  1285. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Syndrome de détresse respiratoire aiguë
    n1=en:roberts syndrome | n2=Syndrome de détresse respiratoire aiguë | rel=r_associated | relid=0 | w=20
  1286. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de douleur extrême paroxystique
    n1=en:roberts syndrome | n2=syndrome de douleur extrême paroxystique | rel=r_associated | relid=0 | w=20
  1287. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de duane
    n1=en:roberts syndrome | n2=syndrome de duane | rel=r_associated | relid=0 | w=20
  1288. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Duane
    n1=en:roberts syndrome | n2=syndrome de Duane | rel=r_associated | relid=0 | w=20
  1289. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Dubin-Johnson
    n1=en:roberts syndrome | n2=syndrome de Dubin-Johnson | rel=r_associated | relid=0 | w=20
  1290. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de dubin-johnson
    n1=en:roberts syndrome | n2=syndrome de dubin-johnson | rel=r_associated | relid=0 | w=20
  1291. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de fragilité du chromosome X
    n1=en:roberts syndrome | n2=syndrome de fragilité du chromosome X | rel=r_associated | relid=0 | w=20
  1292. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de goltz
    n1=en:roberts syndrome | n2=syndrome de goltz | rel=r_associated | relid=0 | w=20
  1293. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Goltz
    n1=en:roberts syndrome | n2=syndrome de Goltz | rel=r_associated | relid=0 | w=20
  1294. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Jacobsen
    n1=en:roberts syndrome | n2=syndrome de Jacobsen | rel=r_associated | relid=0 | w=20
  1295. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de jadassohn-lewandowsky
    n1=en:roberts syndrome | n2=syndrome de jadassohn-lewandowsky | rel=r_associated | relid=0 | w=20
  1296. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Jadassohn-Lewandowsky
    n1=en:roberts syndrome | n2=syndrome de Jadassohn-Lewandowsky | rel=r_associated | relid=0 | w=20
  1297. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de kawasaki
    n1=en:roberts syndrome | n2=syndrome de kawasaki | rel=r_associated | relid=0 | w=20
  1298. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Kawasaki
    n1=en:roberts syndrome | n2=syndrome de Kawasaki | rel=r_associated | relid=0 | w=20
  1299. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Kelly-Paterson
    n1=en:roberts syndrome | n2=syndrome de Kelly-Paterson | rel=r_associated | relid=0 | w=20
  1300. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de l'arc aortique
    n1=en:roberts syndrome | n2=syndrome de l'arc aortique | rel=r_associated | relid=0 | w=20
  1301. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de l'homme rouge
    n1=en:roberts syndrome | n2=syndrome de l'homme rouge | rel=r_associated | relid=0 | w=20
  1302. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de l'immunodéficience acquise
    n1=en:roberts syndrome | n2=syndrome de l'immunodéficience acquise | rel=r_associated | relid=0 | w=20
  1303. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de la crosse aortique
    n1=en:roberts syndrome | n2=syndrome de la crosse aortique | rel=r_associated | relid=0 | w=20
  1304. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de la mort subite du nourrisson
    n1=en:roberts syndrome | n2=syndrome de la mort subite du nourrisson | rel=r_associated | relid=0 | w=20
  1305. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Syndrome de la queue de cheval
    n1=en:roberts syndrome | n2=Syndrome de la queue de cheval | rel=r_associated | relid=0 | w=20
  1306. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de la queue de cheval
    n1=en:roberts syndrome | n2=syndrome de la queue de cheval | rel=r_associated | relid=0 | w=20
  1307. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Laurence-Moon
    n1=en:roberts syndrome | n2=syndrome de Laurence-Moon | rel=r_associated | relid=0 | w=20
  1308. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de li-fraumeni
    n1=en:roberts syndrome | n2=syndrome de li-fraumeni | rel=r_associated | relid=0 | w=20
  1309. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de malabsorption
    n1=en:roberts syndrome | n2=syndrome de malabsorption | rel=r_associated | relid=0 | w=20
  1310. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de marfan
    n1=en:roberts syndrome | n2=syndrome de marfan | rel=r_associated | relid=0 | w=20
  1311. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Martin-Bell
    n1=en:roberts syndrome | n2=syndrome de Martin-Bell | rel=r_associated | relid=0 | w=20
  1312. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de membrane hyaline
    n1=en:roberts syndrome | n2=syndrome de membrane hyaline | rel=r_associated | relid=0 | w=20
  1313. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de plummer-vinson
    n1=en:roberts syndrome | n2=syndrome de plummer-vinson | rel=r_associated | relid=0 | w=20
  1314. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Plummer-Vinson
    n1=en:roberts syndrome | n2=syndrome de Plummer-Vinson | rel=r_associated | relid=0 | w=20
  1315. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Syndrome de Plummer-Vinson
    n1=en:roberts syndrome | n2=Syndrome de Plummer-Vinson | rel=r_associated | relid=0 | w=20
  1316. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Syndrome de Rett
    n1=en:roberts syndrome | n2=Syndrome de Rett | rel=r_associated | relid=0 | w=20
  1317. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de rett
    n1=en:roberts syndrome | n2=syndrome de rett | rel=r_associated | relid=0 | w=20
  1318. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Rett
    n1=en:roberts syndrome | n2=syndrome de Rett | rel=r_associated | relid=0 | w=20
  1319. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Sheehan
    n1=en:roberts syndrome | n2=syndrome de Sheehan | rel=r_associated | relid=0 | w=20
  1320. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Shy-Drager
    n1=en:roberts syndrome | n2=syndrome de Shy-Drager | rel=r_associated | relid=0 | w=20
  1321. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Syndrome de Shy-Drager
    n1=en:roberts syndrome | n2=Syndrome de Shy-Drager | rel=r_associated | relid=0 | w=20
  1322. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de shy-drager
    n1=en:roberts syndrome | n2=syndrome de shy-drager | rel=r_associated | relid=0 | w=20
  1323. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de silver-russell
    n1=en:roberts syndrome | n2=syndrome de silver-russell | rel=r_associated | relid=0 | w=20
  1324. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Silver-Russell
    n1=en:roberts syndrome | n2=syndrome de Silver-Russell | rel=r_associated | relid=0 | w=20
  1325. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de soto
    n1=en:roberts syndrome | n2=syndrome de soto | rel=r_associated | relid=0 | w=20
  1326. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de sotos
    n1=en:roberts syndrome | n2=syndrome de sotos | rel=r_associated | relid=0 | w=20
  1327. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Sotos
    n1=en:roberts syndrome | n2=syndrome de Sotos | rel=r_associated | relid=0 | w=20
  1328. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Stilling-Türk-Duane
    n1=en:roberts syndrome | n2=syndrome de Stilling-Türk-Duane | rel=r_associated | relid=0 | w=20
  1329. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Türk-Stilling-Duane
    n1=en:roberts syndrome | n2=syndrome de Türk-Stilling-Duane | rel=r_associated | relid=0 | w=20
  1330. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de türk-stilling-duane
    n1=en:roberts syndrome | n2=syndrome de türk-stilling-duane | rel=r_associated | relid=0 | w=20
  1331. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Williams
    n1=en:roberts syndrome | n2=syndrome de Williams | rel=r_associated | relid=0 | w=20
  1332. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Zellweger
    n1=en:roberts syndrome | n2=syndrome de Zellweger | rel=r_associated | relid=0 | w=20
  1333. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome des brides amniotiques
    n1=en:roberts syndrome | n2=syndrome des brides amniotiques | rel=r_associated | relid=0 | w=20
  1334. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome des yeux de chat
    n1=en:roberts syndrome | n2=syndrome des yeux de chat | rel=r_associated | relid=0 | w=20
  1335. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome du bébé gris
    n1=en:roberts syndrome | n2=syndrome du bébé gris | rel=r_associated | relid=0 | w=20
  1336. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome du canal tarsien
    n1=en:roberts syndrome | n2=syndrome du canal tarsien | rel=r_associated | relid=0 | w=20
  1337. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome du choc toxique
    n1=en:roberts syndrome | n2=syndrome du choc toxique | rel=r_associated | relid=0 | w=20
  1338. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome du grêle court
    n1=en:roberts syndrome | n2=syndrome du grêle court | rel=r_associated | relid=0 | w=20
  1339. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome du tunnel tarsien
    n1=en:roberts syndrome | n2=syndrome du tunnel tarsien | rel=r_associated | relid=0 | w=20
  1340. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome gris du nourrisson
    n1=en:roberts syndrome | n2=syndrome gris du nourrisson | rel=r_associated | relid=0 | w=20
  1341. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome hémolytique et urémique atypique
    n1=en:roberts syndrome | n2=syndrome hémolytique et urémique atypique | rel=r_associated | relid=0 | w=20
  1342. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome hétérotaxique
    n1=en:roberts syndrome | n2=syndrome hétérotaxique | rel=r_associated | relid=0 | w=20
  1343. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome inflammatoire aigu systémique
    n1=en:roberts syndrome | n2=syndrome inflammatoire aigu systémique | rel=r_associated | relid=0 | w=20
  1344. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome lympho-cutanéo-muqueux
    n1=en:roberts syndrome | n2=syndrome lympho-cutanéo-muqueux | rel=r_associated | relid=0 | w=20
  1345. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome métabolique
    n1=en:roberts syndrome | n2=syndrome métabolique | rel=r_associated | relid=0 | w=20
  1346. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome sec
    n1=en:roberts syndrome | n2=syndrome sec | rel=r_associated | relid=0 | w=20
  1347. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome TORCH
    n1=en:roberts syndrome | n2=syndrome TORCH | rel=r_associated | relid=0 | w=20
  1348. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome torch
    n1=en:roberts syndrome | n2=syndrome torch | rel=r_associated | relid=0 | w=20
  1349. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome tricho-rhino-phalangien de type 2
    n1=en:roberts syndrome | n2=syndrome tricho-rhino-phalangien de type 2 | rel=r_associated | relid=0 | w=20
  1350. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome tricho-rhino-phalangien de type II
    n1=en:roberts syndrome | n2=syndrome tricho-rhino-phalangien de type II | rel=r_associated | relid=0 | w=20
  1351. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> syndrome tricho-rhino-phalangien de type ii
    n1=en:roberts syndrome | n2=syndrome tricho-rhino-phalangien de type ii | rel=r_associated | relid=0 | w=20
  1352. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> télécanthus-hypertélorisme-strabisme (syndrome)
    n1=en:roberts syndrome | n2=télécanthus-hypertélorisme-strabisme (syndrome) | rel=r_associated | relid=0 | w=20
  1353. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> toxémie staphylococcique
    n1=en:roberts syndrome | n2=toxémie staphylococcique | rel=r_associated | relid=0 | w=20
  1354. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> TPN ou NADP
    n1=en:roberts syndrome | n2=TPN ou NADP | rel=r_associated | relid=0 | w=20
  1355. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> trachéo-bronchomégalie
    n1=en:roberts syndrome | n2=trachéo-bronchomégalie | rel=r_associated | relid=0 | w=20
  1356. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> trichothiodystrophie
    n1=en:roberts syndrome | n2=trichothiodystrophie | rel=r_associated | relid=0 | w=20
  1357. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> troubles endocriniens, épilepsie et déficience mentale
    n1=en:roberts syndrome | n2=troubles endocriniens, épilepsie et déficience mentale | rel=r_associated | relid=0 | w=20
  1358. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> tuberculose des méninges
    n1=en:roberts syndrome | n2=tuberculose des méninges | rel=r_associated | relid=0 | w=20
  1359. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> tuberculose méningée
    n1=en:roberts syndrome | n2=tuberculose méningée | rel=r_associated | relid=0 | w=20
  1360. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> tunnel tarsien (syndrome du)
    n1=en:roberts syndrome | n2=tunnel tarsien (syndrome du) | rel=r_associated | relid=0 | w=20
  1361. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Türk-Stilling-Duane (syndrome de)
    n1=en:roberts syndrome | n2=Türk-Stilling-Duane (syndrome de) | rel=r_associated | relid=0 | w=20
  1362. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> van Bogaert (xanthomatose cérébrotendineuse de)
    n1=en:roberts syndrome | n2=van Bogaert (xanthomatose cérébrotendineuse de) | rel=r_associated | relid=0 | w=20
  1363. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> varicelle congénitale
    n1=en:roberts syndrome | n2=varicelle congénitale | rel=r_associated | relid=0 | w=20
  1364. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> ventriculomégalie cérébrale
    n1=en:roberts syndrome | n2=ventriculomégalie cérébrale | rel=r_associated | relid=0 | w=20
  1365. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Walker-Warburg (syndrome de)
    n1=en:roberts syndrome | n2=Walker-Warburg (syndrome de) | rel=r_associated | relid=0 | w=20
  1366. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> wallérienne (dégénérescence)
    n1=en:roberts syndrome | n2=wallérienne (dégénérescence) | rel=r_associated | relid=0 | w=20
  1367. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> Whipple (maladie de)
    n1=en:roberts syndrome | n2=Whipple (maladie de) | rel=r_associated | relid=0 | w=20
  1368. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> xanthomatose cérébro-tendineuse
    n1=en:roberts syndrome | n2=xanthomatose cérébro-tendineuse | rel=r_associated | relid=0 | w=20
  1369. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse
    n1=en:roberts syndrome | n2=xanthomatose cérébrotendineuse | rel=r_associated | relid=0 | w=20
  1370. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse de Van Bogaert
    n1=en:roberts syndrome | n2=xanthomatose cérébrotendineuse de Van Bogaert | rel=r_associated | relid=0 | w=20
  1371. en:roberts syndrome -- r_associated #0: 20 / 0.465 -> yellow nail syndrome
    n1=en:roberts syndrome | n2=yellow nail syndrome | rel=r_associated | relid=0 | w=20
  1372. en:roberts syndrome -- r_associated #0: 4 / 0.093 -> en:rare non-neoplastic disorder
    n1=en:roberts syndrome | n2=en:rare non-neoplastic disorder | rel=r_associated | relid=0 | w=4
≈ 2049 relations entrantes

  1. en:maple syrup urine disease --- r_associated #0: 696 --> en:roberts syndrome
    n1=en:maple syrup urine disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=696
  2. maladie du sirop d'érable --- r_associated #0: 604.37 --> en:roberts syndrome
    n1=maladie du sirop d'érable | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=604.37
  3. leucinose --- r_associated #0: 599.18 --> en:roberts syndrome
    n1=leucinose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=599.18
  4. en:branched-chain ketoaciduria --- r_associated #0: 520 --> en:roberts syndrome
    n1=en:branched-chain ketoaciduria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=520
  5. peste
    (maladie)
     --- r_associated #0: 488 --> en:roberts syndrome
    n1=peste
    (maladie)
    | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=488
  6. en:plague --- r_associated #0: 484 --> en:roberts syndrome
    n1=en:plague | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=484
  7. hypoxémie --- r_associated #0: 436 --> en:roberts syndrome
    n1=hypoxémie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=436
  8. syndrome de Goltz --- r_associated #0: 379 --> en:roberts syndrome
    n1=syndrome de Goltz | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=379
  9. hypoplasie dermique focale --- r_associated #0: 375 --> en:roberts syndrome
    n1=hypoplasie dermique focale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=375
  10. Goltz --- r_associated #0: 374 --> en:roberts syndrome
    n1=Goltz | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=374
  11. hypoplasie dermique en aires --- r_associated #0: 374 --> en:roberts syndrome
    n1=hypoplasie dermique en aires | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=374
  12. en:focal dermal hypoplasia --- r_associated #0: 370 --> en:roberts syndrome
    n1=en:focal dermal hypoplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=370
  13. en:SIDS --- r_associated #0: 355 --> en:roberts syndrome
    n1=en:SIDS | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=355
  14. en:cot death --- r_associated #0: 355 --> en:roberts syndrome
    n1=en:cot death | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=355
  15. mort subite du nourrisson --- r_associated #0: 355 --> en:roberts syndrome
    n1=mort subite du nourrisson | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=355
  16. en:sudden infant death syndrome --- r_associated #0: 354 --> en:roberts syndrome
    n1=en:sudden infant death syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=354
  17. syndrome de la mort subite du nourrisson --- r_associated #0: 345 --> en:roberts syndrome
    n1=syndrome de la mort subite du nourrisson | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=345
  18. syndrome du choc toxique --- r_associated #0: 315 --> en:roberts syndrome
    n1=syndrome du choc toxique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=315
  19. en:toxic shock syndrome --- r_associated #0: 314 --> en:roberts syndrome
    n1=en:toxic shock syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=314
  20. atélectasie congestive --- r_associated #0: 310 --> en:roberts syndrome
    n1=atélectasie congestive | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=310
  21. choc au poumon --- r_associated #0: 310 --> en:roberts syndrome
    n1=choc au poumon | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=310
  22. poumon du vietnam --- r_associated #0: 310 --> en:roberts syndrome
    n1=poumon du vietnam | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=310
  23. insuffisance pulmonaire post-traumatique --- r_associated #0: 309 --> en:roberts syndrome
    n1=insuffisance pulmonaire post-traumatique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=309
  24. micrognathie --- r_associated #0: 304 --> en:roberts syndrome
    n1=micrognathie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=304
  25. oedème du poumon non cardiogénique --- r_associated #0: 304 --> en:roberts syndrome
    n1=oedème du poumon non cardiogénique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=304
  26. oedème pulmonaire non cardiogénique --- r_associated #0: 303 --> en:roberts syndrome
    n1=oedème pulmonaire non cardiogénique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=303
  27. micrognathisme --- r_associated #0: 301 --> en:roberts syndrome
    n1=micrognathisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=301
  28. poumon de choc traumatique --- r_associated #0: 300 --> en:roberts syndrome
    n1=poumon de choc traumatique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=300
  29. en:Toxic Shock Syndrome --- r_associated #0: 295 --> en:roberts syndrome
    n1=en:Toxic Shock Syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=295
  30. en:micrognathism --- r_associated #0: 295 --> en:roberts syndrome
    n1=en:micrognathism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=295
  31. syndrome d'Alagille --- r_associated #0: 289 --> en:roberts syndrome
    n1=syndrome d'Alagille | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=289
  32. en:acute respiratory distress syndrome --- r_associated #0: 288 --> en:roberts syndrome
    n1=en:acute respiratory distress syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=288
  33. en:marfan syndrome --- r_associated #0: 284 --> en:roberts syndrome
    n1=en:marfan syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=284
  34. atrophie optique autosomique dominante --- r_associated #0: 282 --> en:roberts syndrome
    n1=atrophie optique autosomique dominante | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=282
  35. Sars --- r_associated #0: 281 --> en:roberts syndrome
    n1=Sars | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=281
  36. maladie de Marfan --- r_associated #0: 281 --> en:roberts syndrome
    n1=maladie de Marfan | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=281
  37. syndrome de Marfan --- r_associated #0: 281 --> en:roberts syndrome
    n1=syndrome de Marfan | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=281
  38. syndrome de détresse respiratoire aigüe --- r_associated #0: 273 --> en:roberts syndrome
    n1=syndrome de détresse respiratoire aigüe | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=273
  39. poumon de choc --- r_associated #0: 271 --> en:roberts syndrome
    n1=poumon de choc | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=271
  40. en:craniosynostosis --- r_associated #0: 270 --> en:roberts syndrome
    n1=en:craniosynostosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=270
  41. crâniosynostose --- r_associated #0: 266 --> en:roberts syndrome
    n1=crâniosynostose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=266
  42. crâniosténose --- r_associated #0: 265 --> en:roberts syndrome
    n1=crâniosténose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=265
  43. en:crib death --- r_associated #0: 265 --> en:roberts syndrome
    n1=en:crib death | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=265
  44. maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 265 --> en:roberts syndrome
    n1=maladie des urines à l'odeur de sirop d'érable | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=265
  45. crânio-sténose --- r_associated #0: 261 --> en:roberts syndrome
    n1=crânio-sténose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=261
  46. craniosynostose --- r_associated #0: 260 --> en:roberts syndrome
    n1=craniosynostose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=260
  47. en:classical maple syrup urine disease --- r_associated #0: 260 --> en:roberts syndrome
    n1=en:classical maple syrup urine disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=260
  48. en:thiamin-responsive maple syrup urine disease --- r_associated #0: 260 --> en:roberts syndrome
    n1=en:thiamin-responsive maple syrup urine disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=260
  49. maladie des urines avec odeur de sirop erable --- r_associated #0: 260 --> en:roberts syndrome
    n1=maladie des urines avec odeur de sirop erable | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=260
  50. méningite tuberculeuse --- r_associated #0: 258 --> en:roberts syndrome
    n1=méningite tuberculeuse | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=258
  51. déficit en céto-acide décarboxylase --- r_associated #0: 255 --> en:roberts syndrome
    n1=déficit en céto-acide décarboxylase | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=255
  52. en:meningeal tuberculosis --- r_associated #0: 255 --> en:roberts syndrome
    n1=en:meningeal tuberculosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=255
  53. en:tuberculosis of meninges (cerebral)(spinal) --- r_associated #0: 255 --> en:roberts syndrome
    n1=en:tuberculosis of meninges (cerebral)(spinal) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=255
  54. examen non précisé, méningite tuberculeuse --- r_associated #0: 255 --> en:roberts syndrome
    n1=examen non précisé, méningite tuberculeuse | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=255
  55. leptoméningite tuberculeuse --- r_associated #0: 255 --> en:roberts syndrome
    n1=leptoméningite tuberculeuse | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=255
  56. syndrome de détresse respiratoire aiguë --- r_associated #0: 255 --> en:roberts syndrome
    n1=syndrome de détresse respiratoire aiguë | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=255
  57. tuberculose des méninges --- r_associated #0: 255 --> en:roberts syndrome
    n1=tuberculose des méninges | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=255
  58. tuberculose méningée --- r_associated #0: 255 --> en:roberts syndrome
    n1=tuberculose méningée | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=255
  59. en:tuberculosis, meningeal --- r_associated #0: 250 --> en:roberts syndrome
    n1=en:tuberculosis, meningeal | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=250
  60. en:tuberculous hypertrophic pachymeningitides --- r_associated #0: 250 --> en:roberts syndrome
    n1=en:tuberculous hypertrophic pachymeningitides | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=250
  61. en:tuberculous leptomeningitis --- r_associated #0: 250 --> en:roberts syndrome
    n1=en:tuberculous leptomeningitis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=250
  62. pachyméningite hypertrophique tuberculeuse --- r_associated #0: 245 --> en:roberts syndrome
    n1=pachyméningite hypertrophique tuberculeuse | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=245
  63. arachnodactylie --- r_associated #0: 240 --> en:roberts syndrome
    n1=arachnodactylie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=240
  64. maladie de Caffey --- r_associated #0: 230 --> en:roberts syndrome
    n1=maladie de Caffey | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=230
  65. en:arachnodactyly --- r_associated #0: 220 --> en:roberts syndrome
    n1=en:arachnodactyly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=220
  66. méningite tuberculeuse examen non précisé --- r_associated #0: 210 --> en:roberts syndrome
    n1=méningite tuberculeuse examen non précisé | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=210
  67. en:primary progressive aphasia --- r_associated #0: 209 --> en:roberts syndrome
    n1=en:primary progressive aphasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=209
  68. aphasie primaire progressive --- r_associated #0: 208 --> en:roberts syndrome
    n1=aphasie primaire progressive | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=208
  69. aphasies primaires progressives --- r_associated #0: 206 --> en:roberts syndrome
    n1=aphasies primaires progressives | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=206
  70. en:sotos syndrome --- r_associated #0: 191 --> en:roberts syndrome
    n1=en:sotos syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=191
  71. syndrome de soto --- r_associated #0: 190 --> en:roberts syndrome
    n1=syndrome de soto | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=190
  72. gigantisme cérébral --- r_associated #0: 186 --> en:roberts syndrome
    n1=gigantisme cérébral | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=186
  73. craniosténose --- r_associated #0: 185 --> en:roberts syndrome
    n1=craniosténose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=185
  74. syndrome de Sotos --- r_associated #0: 185 --> en:roberts syndrome
    n1=syndrome de Sotos | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=185
  75. en:Plummer-Vinson syndrome --- r_associated #0: 180 --> en:roberts syndrome
    n1=en:Plummer-Vinson syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=180
  76. en:sotos' syndrome --- r_associated #0: 180 --> en:roberts syndrome
    n1=en:sotos' syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=180
  77. en:walker-warburg syndrome --- r_associated #0: 180 --> en:roberts syndrome
    n1=en:walker-warburg syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=180
  78. syndrome de Walker-Warburg --- r_associated #0: 178 --> en:roberts syndrome
    n1=syndrome de Walker-Warburg | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=178
  79. aphasie progressive primaire --- r_associated #0: 177 --> en:roberts syndrome
    n1=aphasie progressive primaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=177
  80. en:plummer-vinson syndrome --- r_associated #0: 177 --> en:roberts syndrome
    n1=en:plummer-vinson syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=177
  81. en:aortic coarctation --- r_associated #0: 176 --> en:roberts syndrome
    n1=en:aortic coarctation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=176
  82. coarctation aortique --- r_associated #0: 175 --> en:roberts syndrome
    n1=coarctation aortique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=175
  83. en:pyruvate carboxylase deficiency --- r_associated #0: 175 --> en:roberts syndrome
    n1=en:pyruvate carboxylase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=175
  84. déficit en pyruvate carboxylase --- r_associated #0: 171 --> en:roberts syndrome
    n1=déficit en pyruvate carboxylase | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=171
  85. en:zellweger syndrome --- r_associated #0: 169 --> en:roberts syndrome
    n1=en:zellweger syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=169
  86. syndrome d'Alport --- r_associated #0: 169 --> en:roberts syndrome
    n1=syndrome d'Alport | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=169
  87. en:Diskinson's syndrome --- r_associated #0: 165 --> en:roberts syndrome
    n1=en:Diskinson's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=165
  88. en:Zellweger syndrome --- r_associated #0: 165 --> en:roberts syndrome
    n1=en:Zellweger syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=165
  89. en:arthrogryposis --- r_associated #0: 156 --> en:roberts syndrome
    n1=en:arthrogryposis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=156
  90. Weir Mitchell --- r_associated #0: 155 --> en:roberts syndrome
    n1=Weir Mitchell | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=155
  91. arthrogrypose --- r_associated #0: 155 --> en:roberts syndrome
    n1=arthrogrypose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=155
  92. paralysies périodiques familiales --- r_associated #0: 153 --> en:roberts syndrome
    n1=paralysies périodiques familiales | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=153
  93. malformation d'Arnold-Chiari --- r_associated #0: 151 --> en:roberts syndrome
    n1=malformation d'Arnold-Chiari | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=151
  94. en:familial periodic paralysis --- r_associated #0: 150 --> en:roberts syndrome
    n1=en:familial periodic paralysis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=150
  95. érythermalgie --- r_associated #0: 146 --> en:roberts syndrome
    n1=érythermalgie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=146
  96. en:arnold chiari malformation --- r_associated #0: 145 --> en:roberts syndrome
    n1=en:arnold chiari malformation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=145
  97. paralysie périodique familiale --- r_associated #0: 145 --> en:roberts syndrome
    n1=paralysie périodique familiale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=145
  98. syndrome de Türk-Stilling-Duane --- r_associated #0: 145 --> en:roberts syndrome
    n1=syndrome de Türk-Stilling-Duane | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=145
  99. érythromélalgie --- r_associated #0: 145 --> en:roberts syndrome
    n1=érythromélalgie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=145
  100. en:erythromelalgia --- r_associated #0: 143 --> en:roberts syndrome
    n1=en:erythromelalgia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=143
  101. en:arnold-chiari malformation --- r_associated #0: 142 --> en:roberts syndrome
    n1=en:arnold-chiari malformation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=142
  102. en:duane syndrome --- r_associated #0: 142 --> en:roberts syndrome
    n1=en:duane syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=142
  103. ostéochondrodysplasies --- r_associated #0: 141 --> en:roberts syndrome
    n1=ostéochondrodysplasies | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=141
  104. syndrome de Duane --- r_associated #0: 141 --> en:roberts syndrome
    n1=syndrome de Duane | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=141
  105. en:osteochondrodysplasia --- r_associated #0: 137 --> en:roberts syndrome
    n1=en:osteochondrodysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=137
  106. erythromelalgia --- r_associated #0: 136 --> en:roberts syndrome
    n1=erythromelalgia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=136
  107. en:whipple disease --- r_associated #0: 134 --> en:roberts syndrome
    n1=en:whipple disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=134
  108. en:mental retardation --- r_associated #0: 133 --> en:roberts syndrome
    n1=en:mental retardation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=133
  109. syndrome de duane --- r_associated #0: 132 --> en:roberts syndrome
    n1=syndrome de duane | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=132
  110. en:angelman syndrome --- r_associated #0: 131 --> en:roberts syndrome
    n1=en:angelman syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=131
  111. en:exophthalmos --- r_associated #0: 131 --> en:roberts syndrome
    n1=en:exophthalmos | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=131
  112. proptose --- r_associated #0: 131 --> en:roberts syndrome
    n1=proptose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=131
  113. retardation mentale --- r_associated #0: 131 --> en:roberts syndrome
    n1=retardation mentale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=131
  114. Retard mental --- r_associated #0: 130 --> en:roberts syndrome
    n1=Retard mental | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=130
  115. exophtalmie --- r_associated #0: 130 --> en:roberts syndrome
    n1=exophtalmie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=130
  116. exophthalmie --- r_associated #0: 130 --> en:roberts syndrome
    n1=exophthalmie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=130
  117. maladie de Whipple --- r_associated #0: 130 --> en:roberts syndrome
    n1=maladie de Whipple | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=130
  118. retard mental --- r_associated #0: 130 --> en:roberts syndrome
    n1=retard mental | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=130
  119. syndrome d'Angelman --- r_associated #0: 130 --> en:roberts syndrome
    n1=syndrome d'Angelman | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=130
  120. ostéopétrose avec acidose rénale tubulaire --- r_associated #0: 128 --> en:roberts syndrome
    n1=ostéopétrose avec acidose rénale tubulaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=128
  121. en:osteopetrosis with renal tubular acidosis --- r_associated #0: 127 --> en:roberts syndrome
    n1=en:osteopetrosis with renal tubular acidosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=127
  122. idiotie spastique amaurotique axonale --- r_associated #0: 117 --> en:roberts syndrome
    n1=idiotie spastique amaurotique axonale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=117
  123. en:cytochrome-c oxidase deficiency --- r_associated #0: 116 --> en:roberts syndrome
    n1=en:cytochrome-c oxidase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=116
  124. démence frontotemporale --- r_associated #0: 115 --> en:roberts syndrome
    n1=démence frontotemporale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=115
  125. déficit en cytochrome oxydase --- r_associated #0: 114 --> en:roberts syndrome
    n1=déficit en cytochrome oxydase | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=114
  126. dystrophie neuroaxonale infantile --- r_associated #0: 113 --> en:roberts syndrome
    n1=dystrophie neuroaxonale infantile | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=113
  127. dystrophie neuroaxonale --- r_associated #0: 111 --> en:roberts syndrome
    n1=dystrophie neuroaxonale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=111
  128. démence fronto-temporale --- r_associated #0: 111 --> en:roberts syndrome
    n1=démence fronto-temporale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=111
  129. dystrophie neuro-axonale infantile --- r_associated #0: 107 --> en:roberts syndrome
    n1=dystrophie neuro-axonale infantile | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=107
  130. en:pulmonary shunting --- r_associated #0: 105 --> en:roberts syndrome
    n1=en:pulmonary shunting | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=105
  131. aïnhum --- r_associated #0: 103 --> en:roberts syndrome
    n1=aïnhum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=103
  132. holoprosencéphalie --- r_associated #0: 102 --> en:roberts syndrome
    n1=holoprosencéphalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=102
  133. syndrome adénocutanéomuqueux --- r_associated #0: 102 --> en:roberts syndrome
    n1=syndrome adénocutanéomuqueux | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=102
  134. dystrophie neuroaxonale de Seitelberger --- r_associated #0: 101 --> en:roberts syndrome
    n1=dystrophie neuroaxonale de Seitelberger | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=101
  135. syndrome de Plummer-Vinson --- r_associated #0: 101 --> en:roberts syndrome
    n1=syndrome de Plummer-Vinson | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=101
  136. syndrome des brides amniotiques --- r_associated #0: 101 --> en:roberts syndrome
    n1=syndrome des brides amniotiques | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=101
  137. en:ainhum --- r_associated #0: 100 --> en:roberts syndrome
    n1=en:ainhum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=100
  138. en:frontotemporal dementia --- r_associated #0: 100 --> en:roberts syndrome
    n1=en:frontotemporal dementia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=100
  139. en:holoprosencephaly --- r_associated #0: 100 --> en:roberts syndrome
    n1=en:holoprosencephaly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=100
  140. en:progressive supranuclear palsy --- r_associated #0: 100 --> en:roberts syndrome
    n1=en:progressive supranuclear palsy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=100
  141. en:yellow nail syndrome --- r_associated #0: 100 --> en:roberts syndrome
    n1=en:yellow nail syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=100
  142. sicca syndrome --- r_associated #0: 100 --> en:roberts syndrome
    n1=sicca syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=100
  143. syndrome de Kawasaki --- r_associated #0: 100 --> en:roberts syndrome
    n1=syndrome de Kawasaki | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=100
  144. syndrome de Rett --- r_associated #0: 100 --> en:roberts syndrome
    n1=syndrome de Rett | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=100
  145. maladie de Kawasaki --- r_associated #0: 99 --> en:roberts syndrome
    n1=maladie de Kawasaki | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=99
  146. anencéphalie --- r_associated #0: 98 --> en:roberts syndrome
    n1=anencéphalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=98
  147. en:alice in wonderland syndrome --- r_associated #0: 98 --> en:roberts syndrome
    n1=en:alice in wonderland syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=98
  148. en:rett syndrome --- r_associated #0: 98 --> en:roberts syndrome
    n1=en:rett syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=98
  149. paralysie supranucléaire progressive --- r_associated #0: 98 --> en:roberts syndrome
    n1=paralysie supranucléaire progressive | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=98
  150. en:amniotic band syndrome --- r_associated #0: 97 --> en:roberts syndrome
    n1=en:amniotic band syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=97
  151. en:anencephaly --- r_associated #0: 97 --> en:roberts syndrome
    n1=en:anencephaly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=97
  152. en:kawasaki disease --- r_associated #0: 97 --> en:roberts syndrome
    n1=en:kawasaki disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=97
  153. en:sicca syndrome --- r_associated #0: 97 --> en:roberts syndrome
    n1=en:sicca syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=97
  154. yellow nail syndrome --- r_associated #0: 97 --> en:roberts syndrome
    n1=yellow nail syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=97
  155. hypertélorisme --- r_associated #0: 96 --> en:roberts syndrome
    n1=hypertélorisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=96
  156. maladies des bandes amniotiques --- r_associated #0: 96 --> en:roberts syndrome
    n1=maladies des bandes amniotiques | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=96
  157. piébaldisme --- r_associated #0: 96 --> en:roberts syndrome
    n1=piébaldisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=96
  158. syndrome adéno-cutanéo-muqueux --- r_associated #0: 96 --> en:roberts syndrome
    n1=syndrome adéno-cutanéo-muqueux | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=96
  159. ainhum --- r_associated #0: 95 --> en:roberts syndrome
    n1=ainhum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=95
  160. déficit en cytochrome-c oxydase --- r_associated #0: 95 --> en:roberts syndrome
    n1=déficit en cytochrome-c oxydase | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=95
  161. en:Alice in Wonderland syndrome --- r_associated #0: 95 --> en:roberts syndrome
    n1=en:Alice in Wonderland syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=95
  162. en:piebaldism --- r_associated #0: 95 --> en:roberts syndrome
    n1=en:piebaldism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=95
  163. en:septo-optic dysplasia --- r_associated #0: 95 --> en:roberts syndrome
    n1=en:septo-optic dysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=95
  164. piebaldisme --- r_associated #0: 95 --> en:roberts syndrome
    n1=piebaldisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=95
  165. progeria --- r_associated #0: 95 --> en:roberts syndrome
    n1=progeria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=95
  166. en:hypertelorism --- r_associated #0: 93 --> en:roberts syndrome
    n1=en:hypertelorism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=93
  167. en:progeria --- r_associated #0: 92 --> en:roberts syndrome
    n1=en:progeria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=92
  168. syndrome lympho-cutanéo-muqueux --- r_associated #0: 92 --> en:roberts syndrome
    n1=syndrome lympho-cutanéo-muqueux | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=92
  169. septo-optic dysplasia --- r_associated #0: 91 --> en:roberts syndrome
    n1=septo-optic dysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=91
  170. syndrome de bride amniotique --- r_associated #0: 91 --> en:roberts syndrome
    n1=syndrome de bride amniotique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=91
  171. en:Angelman syndrome --- r_associated #0: 90 --> en:roberts syndrome
    n1=en:Angelman syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=90
  172. en:jacobsen syndrome --- r_associated #0: 90 --> en:roberts syndrome
    n1=en:jacobsen syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=90
  173. hydrocéphalie --- r_associated #0: 90 --> en:roberts syndrome
    n1=hydrocéphalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=90
  174. polyhydramnios --- r_associated #0: 90 --> en:roberts syndrome
    n1=polyhydramnios | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=90
  175. protéinose alvéolaire --- r_associated #0: 90 --> en:roberts syndrome
    n1=protéinose alvéolaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=90
  176. protéinose alvéolaire pulmonaire --- r_associated #0: 90 --> en:roberts syndrome
    n1=protéinose alvéolaire pulmonaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=90
  177. syndrome de l'immunodéficience acquise --- r_associated #0: 90 --> en:roberts syndrome
    n1=syndrome de l'immunodéficience acquise | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=90
  178. cataplexie --- r_associated #0: 89 --> en:roberts syndrome
    n1=cataplexie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=89
  179. en:polyhydramnios --- r_associated #0: 89 --> en:roberts syndrome
    n1=en:polyhydramnios | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=89
  180. en:cataplexy --- r_associated #0: 88 --> en:roberts syndrome
    n1=en:cataplexy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=88
  181. en:cerebral ventriculomegaly --- r_associated #0: 88 --> en:roberts syndrome
    n1=en:cerebral ventriculomegaly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=88
  182. en:pulmonary alveolar proteinosis --- r_associated #0: 88 --> en:roberts syndrome
    n1=en:pulmonary alveolar proteinosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=88
  183. maladie de Seitelberger --- r_associated #0: 88 --> en:roberts syndrome
    n1=maladie de Seitelberger | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=88
  184. progéria --- r_associated #0: 87 --> en:roberts syndrome
    n1=progéria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=87
  185. Seitelberger --- r_associated #0: 86 --> en:roberts syndrome
    n1=Seitelberger | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=86
  186. en:acquired immunodeficiency syndrome --- r_associated #0: 86 --> en:roberts syndrome
    n1=en:acquired immunodeficiency syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=86
  187. en:ventriculomeglia --- r_associated #0: 86 --> en:roberts syndrome
    n1=en:ventriculomeglia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=86
  188. syndrome de Jacobsen --- r_associated #0: 86 --> en:roberts syndrome
    n1=syndrome de Jacobsen | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=86
  189. syndrome du canal tarsien --- r_associated #0: 86 --> en:roberts syndrome
    n1=syndrome du canal tarsien | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=86
  190. leprosy --- r_associated #0: 85 --> en:roberts syndrome
    n1=leprosy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=85
  191. syndrome d'Alice au pays des merveilles --- r_associated #0: 85 --> en:roberts syndrome
    n1=syndrome d'Alice au pays des merveilles | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=85
  192. syndrome d'immunodéficience acquise --- r_associated #0: 85 --> en:roberts syndrome
    n1=syndrome d'immunodéficience acquise | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=85
  193. en:tarsal tunnel syndrome --- r_associated #0: 84 --> en:roberts syndrome
    n1=en:tarsal tunnel syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=84
  194. hydroa vacciniforme --- r_associated #0: 84 --> en:roberts syndrome
    n1=hydroa vacciniforme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=84
  195. en:hydroa vacciniforme --- r_associated #0: 82 --> en:roberts syndrome
    n1=en:hydroa vacciniforme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=82
  196. ventriculomégalie cérébrale --- r_associated #0: 82 --> en:roberts syndrome
    n1=ventriculomégalie cérébrale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=82
  197. dentinogenesis imperfecta --- r_associated #0: 81 --> en:roberts syndrome
    n1=dentinogenesis imperfecta | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=81
  198. en:leprosy --- r_associated #0: 81 --> en:roberts syndrome
    n1=en:leprosy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=81
  199. Malformation d'Arnold-Chiari --- r_associated #0: 80 --> en:roberts syndrome
    n1=Malformation d'Arnold-Chiari | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=80
  200. brachydactylie --- r_associated #0: 80 --> en:roberts syndrome
    n1=brachydactylie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=80
  201. en:cerebral tuberculosis --- r_associated #0: 80 --> en:roberts syndrome
    n1=en:cerebral tuberculosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=80
  202. en:infantile neuroaxonal dystrophy --- r_associated #0: 80 --> en:roberts syndrome
    n1=en:infantile neuroaxonal dystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=80
  203. en:red man syndrome --- r_associated #0: 79 --> en:roberts syndrome
    n1=en:red man syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=79
  204. en:dentinogenesis imperfecta --- r_associated #0: 78 --> en:roberts syndrome
    n1=en:dentinogenesis imperfecta | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=78
  205. dumping syndrome --- r_associated #0: 77 --> en:roberts syndrome
    n1=dumping syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=77
  206. en:brachydactyly --- r_associated #0: 77 --> en:roberts syndrome
    n1=en:brachydactyly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=77
  207. syndrome de Kelly-Paterson --- r_associated #0: 77 --> en:roberts syndrome
    n1=syndrome de Kelly-Paterson | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=77
  208. syndrome de l'homme rouge --- r_associated #0: 76 --> en:roberts syndrome
    n1=syndrome de l'homme rouge | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=76
  209. SIDA --- r_associated #0: 75 --> en:roberts syndrome
    n1=SIDA | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=75
  210. dystrophies neuroaxonales --- r_associated #0: 75 --> en:roberts syndrome
    n1=dystrophies neuroaxonales | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=75
  211. en:dumping syndrome --- r_associated #0: 75 --> en:roberts syndrome
    n1=en:dumping syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=75
  212. syndrome tricho-rhino-phalangien de type ii --- r_associated #0: 74 --> en:roberts syndrome
    n1=syndrome tricho-rhino-phalangien de type ii | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=74
  213. en:Whipple disease --- r_associated #0: 73 --> en:roberts syndrome
    n1=en:Whipple disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=73
  214. syndrome de türk-stilling-duane --- r_associated #0: 73 --> en:roberts syndrome
    n1=syndrome de türk-stilling-duane | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=73
  215. malformation d'arnold-chiari --- r_associated #0: 72 --> en:roberts syndrome
    n1=malformation d'arnold-chiari | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=72
  216. arriération mentale --- r_associated #0: 71 --> en:roberts syndrome
    n1=arriération mentale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=71
  217. en:fragile x syndrome --- r_associated #0: 71 --> en:roberts syndrome
    n1=en:fragile x syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=71
  218. pityriasis rubra pilaire --- r_associated #0: 71 --> en:roberts syndrome
    n1=pityriasis rubra pilaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=71
  219. syndrome tricho-rhino-phalangien de type 2 --- r_associated #0: 71 --> en:roberts syndrome
    n1=syndrome tricho-rhino-phalangien de type 2 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=71
  220. Pityriasis rubra pilaire --- r_associated #0: 70 --> en:roberts syndrome
    n1=Pityriasis rubra pilaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=70
  221. anasarque foetal --- r_associated #0: 70 --> en:roberts syndrome
    n1=anasarque foetal | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=70
  222. débilité mentale --- r_associated #0: 70 --> en:roberts syndrome
    n1=débilité mentale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=70
  223. en:Klinefelter syndrome --- r_associated #0: 70 --> en:roberts syndrome
    n1=en:Klinefelter syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=70
  224. en:fragile X syndrome --- r_associated #0: 70 --> en:roberts syndrome
    n1=en:fragile X syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=70
  225. en:trichorhinophalangeal syndrome type ii --- r_associated #0: 69 --> en:roberts syndrome
    n1=en:trichorhinophalangeal syndrome type ii | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=69
  226. en:klinefelter syndrome --- r_associated #0: 67 --> en:roberts syndrome
    n1=en:klinefelter syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=67
  227. en:hydrops fetalis --- r_associated #0: 66 --> en:roberts syndrome
    n1=en:hydrops fetalis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=66
  228. en:oculo-respiratory syndrome --- r_associated #0: 66 --> en:roberts syndrome
    n1=en:oculo-respiratory syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=66
  229. Syndrome d'Angelman --- r_associated #0: 65 --> en:roberts syndrome
    n1=Syndrome d'Angelman | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=65
  230. Syndrome de Rett --- r_associated #0: 65 --> en:roberts syndrome
    n1=Syndrome de Rett | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=65
  231. en:AIDS --- r_associated #0: 65 --> en:roberts syndrome
    n1=en:AIDS | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=65
  232. en:Kawasaki disease --- r_associated #0: 65 --> en:roberts syndrome
    n1=en:Kawasaki disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=65
  233. syndrome de fragilité du chromosome X --- r_associated #0: 65 --> en:roberts syndrome
    n1=syndrome de fragilité du chromosome X | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=65
  234. antisida --- r_associated #0: 64 --> en:roberts syndrome
    n1=antisida | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=64
  235. en:hurler syndrome --- r_associated #0: 64 --> en:roberts syndrome
    n1=en:hurler syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=64
  236. anti-sida --- r_associated #0: 63 --> en:roberts syndrome
    n1=anti-sida | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=63
  237. en:erythermalgia --- r_associated #0: 63 --> en:roberts syndrome
    n1=en:erythermalgia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=63
  238. en:dubin-johnson syndrome --- r_associated #0: 62 --> en:roberts syndrome
    n1=en:dubin-johnson syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=62
  239. en:oculorespiratory syndrome --- r_associated #0: 62 --> en:roberts syndrome
    n1=en:oculorespiratory syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=62
  240. algodystrophies --- r_associated #0: 61 --> en:roberts syndrome
    n1=algodystrophies | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=61
  241. DentinoGenesis Imperfecta --- r_associated #0: 60 --> en:roberts syndrome
    n1=DentinoGenesis Imperfecta | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=60
  242. en:Hurler syndrome --- r_associated #0: 60 --> en:roberts syndrome
    n1=en:Hurler syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=60
  243. en:Sotos' syndrome --- r_associated #0: 60 --> en:roberts syndrome
    n1=en:Sotos' syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=60
  244. en:immune deficiency syndrome --- r_associated #0: 60 --> en:roberts syndrome
    n1=en:immune deficiency syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=60
  245. en:mucocutaneous lymph node syndrome --- r_associated #0: 60 --> en:roberts syndrome
    n1=en:mucocutaneous lymph node syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=60
  246. syndrome de dubin-johnson --- r_associated #0: 60 --> en:roberts syndrome
    n1=syndrome de dubin-johnson | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=60
  247. en:Korsakoff syndrome --- r_associated #0: 59 --> en:roberts syndrome
    n1=en:Korsakoff syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=59
  248. en:guillain-barre syndrome --- r_associated #0: 59 --> en:roberts syndrome
    n1=en:guillain-barre syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=59
  249. en:korsakoff syndrome --- r_associated #0: 59 --> en:roberts syndrome
    n1=en:korsakoff syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=59
  250. syndrome d'angelman --- r_associated #0: 59 --> en:roberts syndrome
    n1=syndrome d'angelman | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=59
  251. acromégalie --- r_associated #0: 58 --> en:roberts syndrome
    n1=acromégalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=58
  252. en:Guillain-Barre syndrome --- r_associated #0: 57 --> en:roberts syndrome
    n1=en:Guillain-Barre syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=57
  253. syndrome de rett --- r_associated #0: 57 --> en:roberts syndrome
    n1=syndrome de rett | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=57
  254. syndrome de la queue de cheval --- r_associated #0: 56 --> en:roberts syndrome
    n1=syndrome de la queue de cheval | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=56
  255. trachéo-bronchomégalie --- r_associated #0: 56 --> en:roberts syndrome
    n1=trachéo-bronchomégalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=56
  256. dystrophies neuro-axonales --- r_associated #0: 55 --> en:roberts syndrome
    n1=dystrophies neuro-axonales | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=55
  257. en:alport syndrome --- r_associated #0: 55 --> en:roberts syndrome
    n1=en:alport syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=55
  258. en:disease aids --- r_associated #0: 55 --> en:roberts syndrome
    n1=en:disease aids | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=55
  259. en:torch syndrome --- r_associated #0: 55 --> en:roberts syndrome
    n1=en:torch syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=55
  260. syndrome tricho-rhino-phalangien de type II --- r_associated #0: 55 --> en:roberts syndrome
    n1=syndrome tricho-rhino-phalangien de type II | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=55
  261. en:acromegaly --- r_associated #0: 54 --> en:roberts syndrome
    n1=en:acromegaly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=54
  262. en:glutaric acidemia type 1 --- r_associated #0: 53 --> en:roberts syndrome
    n1=en:glutaric acidemia type 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=53
  263. en:cauda equina syndrome --- r_associated #0: 52 --> en:roberts syndrome
    n1=en:cauda equina syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=52
  264. en:tracheobronchomegaly --- r_associated #0: 52 --> en:roberts syndrome
    n1=en:tracheobronchomegaly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=52
  265. syndrome d'alport --- r_associated #0: 52 --> en:roberts syndrome
    n1=syndrome d'alport | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=52
  266. syndrome de Dubin-Johnson --- r_associated #0: 52 --> en:roberts syndrome
    n1=syndrome de Dubin-Johnson | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=52
  267. syndrome de silver-russell --- r_associated #0: 52 --> en:roberts syndrome
    n1=syndrome de silver-russell | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=52
  268. acidurie glutarique de type 1 --- r_associated #0: 51 --> en:roberts syndrome
    n1=acidurie glutarique de type 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=51
  269. dentine opalescente héréditaire --- r_associated #0: 51 --> en:roberts syndrome
    n1=dentine opalescente héréditaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=51
  270. en:AIDS awareness --- r_associated #0: 51 --> en:roberts syndrome
    n1=en:AIDS awareness | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=51
  271. en:cardio-facio-cutaneous syndrome --- r_associated #0: 51 --> en:roberts syndrome
    n1=en:cardio-facio-cutaneous syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=51
  272. en:down syndrome --- r_associated #0: 51 --> en:roberts syndrome
    n1=en:down syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=51
  273. en:pick's disease --- r_associated #0: 51 --> en:roberts syndrome
    n1=en:pick's disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=51
  274. en:tay-sachs disease --- r_associated #0: 51 --> en:roberts syndrome
    n1=en:tay-sachs disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=51
  275. peste --- r_associated #0: 51 --> en:roberts syndrome
    n1=peste | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=51
  276. red man syndrome --- r_associated #0: 51 --> en:roberts syndrome
    n1=red man syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=51
  277. syndrome TORCH --- r_associated #0: 51 --> en:roberts syndrome
    n1=syndrome TORCH | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=51
  278. xanthomatose cérébro-tendineuse --- r_associated #0: 51 --> en:roberts syndrome
    n1=xanthomatose cérébro-tendineuse | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=51
  279. xanthomatose cérébrotendineuse --- r_associated #0: 51 --> en:roberts syndrome
    n1=xanthomatose cérébrotendineuse | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=51
  280. Syndrome de la queue de cheval --- r_associated #0: 50 --> en:roberts syndrome
    n1=Syndrome de la queue de cheval | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=50
  281. association toxoplasmose, rubéole, cytomégalovirus et herpès chez un nouveau-né --- r_associated #0: 50 --> en:roberts syndrome
    n1=association toxoplasmose, rubéole, cytomégalovirus et herpès chez un nouveau-né | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=50
  282. cœur triatrial --- r_associated #0: 50 --> en:roberts syndrome
    n1=cœur triatrial | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=50
  283. en:Down syndrome --- r_associated #0: 50 --> en:roberts syndrome
    n1=en:Down syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=50
  284. en:Pick's disease --- r_associated #0: 50 --> en:roberts syndrome
    n1=en:Pick's disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=50
  285. en:Tay-Sachs disease --- r_associated #0: 50 --> en:roberts syndrome
    n1=en:Tay-Sachs disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=50
  286. en:schock lung --- r_associated #0: 50 --> en:roberts syndrome
    n1=en:schock lung | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=50
  287. hydrops fœtoplacentaire --- r_associated #0: 50 --> en:roberts syndrome
    n1=hydrops fœtoplacentaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=50
  288. queue de cheval (syndrome de la) --- r_associated #0: 50 --> en:roberts syndrome
    n1=queue de cheval (syndrome de la) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=50
  289. sirop d'érable (urine à odeur de) --- r_associated #0: 50 --> en:roberts syndrome
    n1=sirop d'érable (urine à odeur de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=50
  290. syndrome de Silver-Russell --- r_associated #0: 50 --> en:roberts syndrome
    n1=syndrome de Silver-Russell | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=50
  291. syndrome de chasse --- r_associated #0: 50 --> en:roberts syndrome
    n1=syndrome de chasse | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=50
  292. syndrome hétérotaxique --- r_associated #0: 50 --> en:roberts syndrome
    n1=syndrome hétérotaxique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=50
  293. syndrome torch --- r_associated #0: 50 --> en:roberts syndrome
    n1=syndrome torch | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=50
  294. en:alveolar proteinosis --- r_associated #0: 49 --> en:roberts syndrome
    n1=en:alveolar proteinosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=49
  295. en:proptosis --- r_associated #0: 49 --> en:roberts syndrome
    n1=en:proptosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=49
  296. hydrops foetoplacentaire --- r_associated #0: 49 --> en:roberts syndrome
    n1=hydrops foetoplacentaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=49
  297. maladie de marfan --- r_associated #0: 49 --> en:roberts syndrome
    n1=maladie de marfan | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=49
  298. névrite optique --- r_associated #0: 49 --> en:roberts syndrome
    n1=névrite optique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=49
  299. toxémie staphylococcique --- r_associated #0: 49 --> en:roberts syndrome
    n1=toxémie staphylococcique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=49
  300. S.I.D.A. --- r_associated #0: 48 --> en:roberts syndrome
    n1=S.I.D.A. | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=48
  301. en:heterotaxy syndrome --- r_associated #0: 48 --> en:roberts syndrome
    n1=en:heterotaxy syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=48
  302. en:hydrencephalus --- r_associated #0: 48 --> en:roberts syndrome
    n1=en:hydrencephalus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=48
  303. en:ophthalmoneuritis --- r_associated #0: 48 --> en:roberts syndrome
    n1=en:ophthalmoneuritis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=48
  304. syndrome de shy-drager --- r_associated #0: 48 --> en:roberts syndrome
    n1=syndrome de shy-drager | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=48
  305. syndrome de sotos --- r_associated #0: 48 --> en:roberts syndrome
    n1=syndrome de sotos | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=48
  306. syndrome des yeux de chat --- r_associated #0: 48 --> en:roberts syndrome
    n1=syndrome des yeux de chat | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=48
  307. tunnel tarsien (syndrome du) --- r_associated #0: 48 --> en:roberts syndrome
    n1=tunnel tarsien (syndrome du) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=48
  308. Syndrome de Shy-Drager --- r_associated #0: 47 --> en:roberts syndrome
    n1=Syndrome de Shy-Drager | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=47
  309. Türk-Stilling-Duane (syndrome de) --- r_associated #0: 47 --> en:roberts syndrome
    n1=Türk-Stilling-Duane (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=47
  310. acidémie glutarique de type 1 --- r_associated #0: 47 --> en:roberts syndrome
    n1=acidémie glutarique de type 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=47
  311. en:cardiofaciocutaneous syndrome --- r_associated #0: 47 --> en:roberts syndrome
    n1=en:cardiofaciocutaneous syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=47
  312. en:cerebrotendinous xanthomatosis --- r_associated #0: 47 --> en:roberts syndrome
    n1=en:cerebrotendinous xanthomatosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=47
  313. en:optic neuritis --- r_associated #0: 47 --> en:roberts syndrome
    n1=en:optic neuritis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=47
  314. hypertélorisme-microtie-fente faciale --- r_associated #0: 47 --> en:roberts syndrome
    n1=hypertélorisme-microtie-fente faciale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=47
  315. syndrome de la crosse aortique --- r_associated #0: 47 --> en:roberts syndrome
    n1=syndrome de la crosse aortique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=47
  316. syndrome du tunnel tarsien --- r_associated #0: 47 --> en:roberts syndrome
    n1=syndrome du tunnel tarsien | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=47
  317. acromegaly --- r_associated #0: 46 --> en:roberts syndrome
    n1=acromegaly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=46
  318. coeur triatrial --- r_associated #0: 46 --> en:roberts syndrome
    n1=coeur triatrial | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=46
  319. en:cat-eye syndrome --- r_associated #0: 46 --> en:roberts syndrome
    n1=en:cat-eye syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=46
  320. en:pityriasis rubra pilaris --- r_associated #0: 46 --> en:roberts syndrome
    n1=en:pityriasis rubra pilaris | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=46
  321. en:prader-willi syndrome --- r_associated #0: 46 --> en:roberts syndrome
    n1=en:prader-willi syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=46
  322. en:situs inversus --- r_associated #0: 46 --> en:roberts syndrome
    n1=en:situs inversus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=46
  323. en:trichorhinophalangeal syndrome type II --- r_associated #0: 46 --> en:roberts syndrome
    n1=en:trichorhinophalangeal syndrome type II | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=46
  324. retard mental, retard de croissance, surdité, microgénitalisme lié au sexe --- r_associated #0: 46 --> en:roberts syndrome
    n1=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=46
  325. situs inversus --- r_associated #0: 46 --> en:roberts syndrome
    n1=situs inversus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=46
  326. wallérienne (dégénérescence) --- r_associated #0: 46 --> en:roberts syndrome
    n1=wallérienne (dégénérescence) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=46
  327. en:Kawasaki's syndrome --- r_associated #0: 45 --> en:roberts syndrome
    n1=en:Kawasaki's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  328. en:Prader-Willi syndrome --- r_associated #0: 45 --> en:roberts syndrome
    n1=en:Prader-Willi syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  329. en:aortic arch syndrome --- r_associated #0: 45 --> en:roberts syndrome
    n1=en:aortic arch syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  330. en:russell-silver syndrome --- r_associated #0: 45 --> en:roberts syndrome
    n1=en:russell-silver syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  331. en:situs mutatus --- r_associated #0: 45 --> en:roberts syndrome
    n1=en:situs mutatus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  332. en:stokes-adams syndrome --- r_associated #0: 45 --> en:roberts syndrome
    n1=en:stokes-adams syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  333. en:wallerian degeneration --- r_associated #0: 45 --> en:roberts syndrome
    n1=en:wallerian degeneration | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  334. hypertélorisme, hypospadias, polysyndactylie (syndrome) --- r_associated #0: 45 --> en:roberts syndrome
    n1=hypertélorisme, hypospadias, polysyndactylie (syndrome) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  335. hétérotaxie --- r_associated #0: 45 --> en:roberts syndrome
    n1=hétérotaxie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  336. maladie de Dercum --- r_associated #0: 45 --> en:roberts syndrome
    n1=maladie de Dercum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  337. maladie de Hurler --- r_associated #0: 45 --> en:roberts syndrome
    n1=maladie de Hurler | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  338. psychose de korsakoff --- r_associated #0: 45 --> en:roberts syndrome
    n1=psychose de korsakoff | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  339. scléromyxœdème d'Arndt-Gottron --- r_associated #0: 45 --> en:roberts syndrome
    n1=scléromyxœdème d'Arndt-Gottron | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  340. scléromyxoedème d'Arndt-Gottron --- r_associated #0: 45 --> en:roberts syndrome
    n1=scléromyxoedème d'Arndt-Gottron | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  341. syndrome de Shy-Drager --- r_associated #0: 45 --> en:roberts syndrome
    n1=syndrome de Shy-Drager | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  342. xanthomatose cérébrotendineuse de Van Bogaert --- r_associated #0: 45 --> en:roberts syndrome
    n1=xanthomatose cérébrotendineuse de Van Bogaert | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=45
  343. en:Stokes-Adams syndrome --- r_associated #0: 44 --> en:roberts syndrome
    n1=en:Stokes-Adams syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=44
  344. en:chondrodysplasia punctata --- r_associated #0: 44 --> en:roberts syndrome
    n1=en:chondrodysplasia punctata | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=44
  345. en:maple-tree syrup disease --- r_associated #0: 44 --> en:roberts syndrome
    n1=en:maple-tree syrup disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=44
  346. phacomatose congenitale --- r_associated #0: 44 --> en:roberts syndrome
    n1=phacomatose congenitale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=44
  347. syndrome de l'arc aortique --- r_associated #0: 44 --> en:roberts syndrome
    n1=syndrome de l'arc aortique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=44
  348. en:carbohydrate-deficient glycoprotein syndrome --- r_associated #0: 43 --> en:roberts syndrome
    n1=en:carbohydrate-deficient glycoprotein syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=43
  349. en:mobius syndrome --- r_associated #0: 43 --> en:roberts syndrome
    n1=en:mobius syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=43
  350. en:multiple acyl-coa dehydrogenase deficiency --- r_associated #0: 43 --> en:roberts syndrome
    n1=en:multiple acyl-coa dehydrogenase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=43
  351. en:oeis complex --- r_associated #0: 43 --> en:roberts syndrome
    n1=en:oeis complex | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=43
  352. en:trigger finger disorder --- r_associated #0: 43 --> en:roberts syndrome
    n1=en:trigger finger disorder | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=43
  353. maladie de Roger --- r_associated #0: 43 --> en:roberts syndrome
    n1=maladie de Roger | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=43
  354. syndrome d'Adair-Dighton --- r_associated #0: 43 --> en:roberts syndrome
    n1=syndrome d'Adair-Dighton | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=43
  355. varicelle congénitale --- r_associated #0: 43 --> en:roberts syndrome
    n1=varicelle congénitale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=43
  356. dysostose craniofaciale --- r_associated #0: 42 --> en:roberts syndrome
    n1=dysostose craniofaciale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=42
  357. en:berardinelli-seip congenital lipodystrophy --- r_associated #0: 42 --> en:roberts syndrome
    n1=en:berardinelli-seip congenital lipodystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=42
  358. en:congenital varicella syndrome --- r_associated #0: 42 --> en:roberts syndrome
    n1=en:congenital varicella syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=42
  359. en:cranioectodermal dysplasia --- r_associated #0: 42 --> en:roberts syndrome
    n1=en:cranioectodermal dysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=42
  360. en:macrophage activation syndrome --- r_associated #0: 42 --> en:roberts syndrome
    n1=en:macrophage activation syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=42
  361. en:wiskott-aldrich syndrome --- r_associated #0: 42 --> en:roberts syndrome
    n1=en:wiskott-aldrich syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=42
  362. syndrome de Jadassohn-Lewandowsky --- r_associated #0: 42 --> en:roberts syndrome
    n1=syndrome de Jadassohn-Lewandowsky | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=42
  363. Syndrome de Plummer-Vinson --- r_associated #0: 41 --> en:roberts syndrome
    n1=Syndrome de Plummer-Vinson | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  364. agnosie --- r_associated #0: 41 --> en:roberts syndrome
    n1=agnosie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  365. anasarque foeto-placentaire --- r_associated #0: 41 --> en:roberts syndrome
    n1=anasarque foeto-placentaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  366. chondrodysplasia punctata --- r_associated #0: 41 --> en:roberts syndrome
    n1=chondrodysplasia punctata | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  367. déficit en protéine trifonctionnelle mitochondriale --- r_associated #0: 41 --> en:roberts syndrome
    n1=déficit en protéine trifonctionnelle mitochondriale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  368. en:Marfan's syndrome --- r_associated #0: 41 --> en:roberts syndrome
    n1=en:Marfan's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  369. en:abstinence syndrome --- r_associated #0: 41 --> en:roberts syndrome
    n1=en:abstinence syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  370. en:adiposis dolorosa --- r_associated #0: 41 --> en:roberts syndrome
    n1=en:adiposis dolorosa | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  371. en:agnosia --- r_associated #0: 41 --> en:roberts syndrome
    n1=en:agnosia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  372. en:ataxia-telangiectasisa-like disorder 1 --- r_associated #0: 41 --> en:roberts syndrome
    n1=en:ataxia-telangiectasisa-like disorder 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  373. en:beta-methylcrotonylglycinuria --- r_associated #0: 41 --> en:roberts syndrome
    n1=en:beta-methylcrotonylglycinuria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  374. en:hair tourniquet --- r_associated #0: 41 --> en:roberts syndrome
    n1=en:hair tourniquet | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  375. en:kearns-sayre syndrome --- r_associated #0: 41 --> en:roberts syndrome
    n1=en:kearns-sayre syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  376. en:maroteaux-lamy syndrome --- r_associated #0: 41 --> en:roberts syndrome
    n1=en:maroteaux-lamy syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  377. en:meckel-gruber syndrome --- r_associated #0: 41 --> en:roberts syndrome
    n1=en:meckel-gruber syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  378. en:pachyonychia congenita --- r_associated #0: 41 --> en:roberts syndrome
    n1=en:pachyonychia congenita | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  379. en:scleromyxedema --- r_associated #0: 41 --> en:roberts syndrome
    n1=en:scleromyxedema | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  380. en:transposition of great vessels --- r_associated #0: 41 --> en:roberts syndrome
    n1=en:transposition of great vessels | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  381. imperforation anale --- r_associated #0: 41 --> en:roberts syndrome
    n1=imperforation anale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  382. syndrome de douleur extrême paroxystique --- r_associated #0: 41 --> en:roberts syndrome
    n1=syndrome de douleur extrême paroxystique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  383. syndrome de goltz --- r_associated #0: 41 --> en:roberts syndrome
    n1=syndrome de goltz | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  384. syndrome de kawasaki --- r_associated #0: 41 --> en:roberts syndrome
    n1=syndrome de kawasaki | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  385. syndrome de marfan --- r_associated #0: 41 --> en:roberts syndrome
    n1=syndrome de marfan | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  386. syndrome du grêle court --- r_associated #0: 41 --> en:roberts syndrome
    n1=syndrome du grêle court | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  387. syndrome sec --- r_associated #0: 41 --> en:roberts syndrome
    n1=syndrome sec | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  388. télécanthus-hypertélorisme-strabisme (syndrome) --- r_associated #0: 41 --> en:roberts syndrome
    n1=télécanthus-hypertélorisme-strabisme (syndrome) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=41
  389. Walker-Warburg (syndrome de) --- r_associated #0: 40 --> en:roberts syndrome
    n1=Walker-Warburg (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  390. Whipple (maladie de) --- r_associated #0: 40 --> en:roberts syndrome
    n1=Whipple (maladie de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  391. anasarque foetoplacentaire --- r_associated #0: 40 --> en:roberts syndrome
    n1=anasarque foetoplacentaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  392. dysostose crânio-faciale --- r_associated #0: 40 --> en:roberts syndrome
    n1=dysostose crânio-faciale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  393. dysplasie olfacto-génitale --- r_associated #0: 40 --> en:roberts syndrome
    n1=dysplasie olfacto-génitale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  394. en:Devergie's disease --- r_associated #0: 40 --> en:roberts syndrome
    n1=en:Devergie's disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  395. en:benign mucous membrane pemphigoid --- r_associated #0: 40 --> en:roberts syndrome
    n1=en:benign mucous membrane pemphigoid | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  396. en:black death --- r_associated #0: 40 --> en:roberts syndrome
    n1=en:black death | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  397. en:black plague --- r_associated #0: 40 --> en:roberts syndrome
    n1=en:black plague | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  398. en:dysequilibrium syndrome --- r_associated #0: 40 --> en:roberts syndrome
    n1=en:dysequilibrium syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  399. en:ectodermal dysplasia --- r_associated #0: 40 --> en:roberts syndrome
    n1=en:ectodermal dysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  400. en:melnick-fraser syndrome --- r_associated #0: 40 --> en:roberts syndrome
    n1=en:melnick-fraser syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  401. en:short bowel syndrome --- r_associated #0: 40 --> en:roberts syndrome
    n1=en:short bowel syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  402. en:shy-drager syndrome --- r_associated #0: 40 --> en:roberts syndrome
    n1=en:shy-drager syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  403. en:superior mesenteric artery syndrome --- r_associated #0: 40 --> en:roberts syndrome
    n1=en:superior mesenteric artery syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  404. en:williams syndrome --- r_associated #0: 40 --> en:roberts syndrome
    n1=en:williams syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  405. holoprosencéphalie de type 3 --- r_associated #0: 40 --> en:roberts syndrome
    n1=holoprosencéphalie de type 3 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  406. hydroa vacciniforme de Bazin --- r_associated #0: 40 --> en:roberts syndrome
    n1=hydroa vacciniforme de Bazin | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  407. intolérance au fructose --- r_associated #0: 40 --> en:roberts syndrome
    n1=intolérance au fructose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  408. lèpre --- r_associated #0: 40 --> en:roberts syndrome
    n1=lèpre | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  409. maladie de Tay-sachs --- r_associated #0: 40 --> en:roberts syndrome
    n1=maladie de Tay-sachs | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  410. maladie de tay-sachs --- r_associated #0: 40 --> en:roberts syndrome
    n1=maladie de tay-sachs | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  411. maladie de whipple --- r_associated #0: 40 --> en:roberts syndrome
    n1=maladie de whipple | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  412. maladie lysosomique de surcharge --- r_associated #0: 40 --> en:roberts syndrome
    n1=maladie lysosomique de surcharge | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  413. peste noire --- r_associated #0: 40 --> en:roberts syndrome
    n1=peste noire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=40
  414. Plummer-Vinson (syndrome de) --- r_associated #0: 39 --> en:roberts syndrome
    n1=Plummer-Vinson (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  415. Silver-Russell (syndrome de) --- r_associated #0: 39 --> en:roberts syndrome
    n1=Silver-Russell (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  416. Syndrome de détresse respiratoire aiguë --- r_associated #0: 39 --> en:roberts syndrome
    n1=Syndrome de détresse respiratoire aiguë | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  417. en:Duane's syndrome --- r_associated #0: 39 --> en:roberts syndrome
    n1=en:Duane's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  418. en:imperforate anus --- r_associated #0: 39 --> en:roberts syndrome
    n1=en:imperforate anus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  419. en:li-fraumeni syndrome --- r_associated #0: 39 --> en:roberts syndrome
    n1=en:li-fraumeni syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  420. en:mitochondrial trifunctional protein deficiency --- r_associated #0: 39 --> en:roberts syndrome
    n1=en:mitochondrial trifunctional protein deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  421. en:multicentric osteolysis, nodulosis, and arthropathy --- r_associated #0: 39 --> en:roberts syndrome
    n1=en:multicentric osteolysis, nodulosis, and arthropathy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  422. en:paroxysmal extreme pain disorder --- r_associated #0: 39 --> en:roberts syndrome
    n1=en:paroxysmal extreme pain disorder | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  423. en:protopsis --- r_associated #0: 39 --> en:roberts syndrome
    n1=en:protopsis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  424. en:ventricular septal defect --- r_associated #0: 39 --> en:roberts syndrome
    n1=en:ventricular septal defect | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  425. en:west syndrome --- r_associated #0: 39 --> en:roberts syndrome
    n1=en:west syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  426. holoprosencéphalie de type 2 --- r_associated #0: 39 --> en:roberts syndrome
    n1=holoprosencéphalie de type 2 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  427. ichtyose --- r_associated #0: 39 --> en:roberts syndrome
    n1=ichtyose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  428. imperforation de l'anus --- r_associated #0: 39 --> en:roberts syndrome
    n1=imperforation de l'anus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  429. ongles jaunes (syndrome des) --- r_associated #0: 39 --> en:roberts syndrome
    n1=ongles jaunes (syndrome des) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  430. protoproporphyrie érythropoïétique --- r_associated #0: 39 --> en:roberts syndrome
    n1=protoproporphyrie érythropoïétique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  431. syndrome de Stilling-Türk-Duane --- r_associated #0: 39 --> en:roberts syndrome
    n1=syndrome de Stilling-Türk-Duane | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  432. trichothiodystrophie --- r_associated #0: 39 --> en:roberts syndrome
    n1=trichothiodystrophie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=39
  433. ectrodactylie --- r_associated #0: 38 --> en:roberts syndrome
    n1=ectrodactylie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  434. en:Black death --- r_associated #0: 38 --> en:roberts syndrome
    n1=en:Black death | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  435. en:Triple a syndrome --- r_associated #0: 38 --> en:roberts syndrome
    n1=en:Triple a syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  436. en:adenocutanemucous syndrome --- r_associated #0: 38 --> en:roberts syndrome
    n1=en:adenocutanemucous syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  437. en:alpha thalassemia x-linked mental retardation syndrome --- r_associated #0: 38 --> en:roberts syndrome
    n1=en:alpha thalassemia x-linked mental retardation syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  438. en:apl differentiation syndrome --- r_associated #0: 38 --> en:roberts syndrome
    n1=en:apl differentiation syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  439. en:cushing syndrome --- r_associated #0: 38 --> en:roberts syndrome
    n1=en:cushing syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  440. en:sheehan syndrome --- r_associated #0: 38 --> en:roberts syndrome
    n1=en:sheehan syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  441. en:tuberculous meningitis --- r_associated #0: 38 --> en:roberts syndrome
    n1=en:tuberculous meningitis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  442. holoprosencéphalie de type 4 --- r_associated #0: 38 --> en:roberts syndrome
    n1=holoprosencéphalie de type 4 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  443. hérédité autosomale récessive --- r_associated #0: 38 --> en:roberts syndrome
    n1=hérédité autosomale récessive | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  444. ictère nucléaire --- r_associated #0: 38 --> en:roberts syndrome
    n1=ictère nucléaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  445. maladie de seitelberger --- r_associated #0: 38 --> en:roberts syndrome
    n1=maladie de seitelberger | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  446. maladie des épiphyses ponctuées --- r_associated #0: 38 --> en:roberts syndrome
    n1=maladie des épiphyses ponctuées | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  447. nevrilème --- r_associated #0: 38 --> en:roberts syndrome
    n1=nevrilème | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  448. ostéochondrodysplasie --- r_associated #0: 38 --> en:roberts syndrome
    n1=ostéochondrodysplasie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  449. syndrome de jadassohn-lewandowsky --- r_associated #0: 38 --> en:roberts syndrome
    n1=syndrome de jadassohn-lewandowsky | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=38
  450. Sotos (syndrome de) --- r_associated #0: 37 --> en:roberts syndrome
    n1=Sotos (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  451. communication inter-auriculaire --- r_associated #0: 37 --> en:roberts syndrome
    n1=communication inter-auriculaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  452. dysplasie ectodermique, ectrodactylie et dystrophie maculaire --- r_associated #0: 37 --> en:roberts syndrome
    n1=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  453. dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental --- r_associated #0: 37 --> en:roberts syndrome
    n1=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  454. dystrophie orbitaire congénitale --- r_associated #0: 37 --> en:roberts syndrome
    n1=dystrophie orbitaire congénitale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  455. déficience intellectuelle --- r_associated #0: 37 --> en:roberts syndrome
    n1=déficience intellectuelle | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  456. en:acyl-coa dehydrogenase, short-chain deficiency --- r_associated #0: 37 --> en:roberts syndrome
    n1=en:acyl-coa dehydrogenase, short-chain deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  457. en:autosomal recessive inheritance --- r_associated #0: 37 --> en:roberts syndrome
    n1=en:autosomal recessive inheritance | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  458. en:cataplexis --- r_associated #0: 37 --> en:roberts syndrome
    n1=en:cataplexis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  459. en:erythropoietic protoporphyria --- r_associated #0: 37 --> en:roberts syndrome
    n1=en:erythropoietic protoporphyria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  460. en:hereditary fructose intolerance --- r_associated #0: 37 --> en:roberts syndrome
    n1=en:hereditary fructose intolerance | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  461. en:heterotaxy --- r_associated #0: 37 --> en:roberts syndrome
    n1=en:heterotaxy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  462. en:kernicterus --- r_associated #0: 37 --> en:roberts syndrome
    n1=en:kernicterus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  463. en:lysosomal storage disease --- r_associated #0: 37 --> en:roberts syndrome
    n1=en:lysosomal storage disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  464. en:morquio syndrome --- r_associated #0: 37 --> en:roberts syndrome
    n1=en:morquio syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  465. en:presence of severe midfacial and limb defects and birth length less than 37cm associated with stillborn or early infant death --- r_associated #0: 37 --> en:roberts syndrome
    n1=en:presence of severe midfacial and limb defects and birth length less than 37cm associated with stillborn or early infant death | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  466. en:sacral agenesis --- r_associated #0: 37 --> en:roberts syndrome
    n1=en:sacral agenesis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  467. en:smith-magenis syndrome --- r_associated #0: 37 --> en:roberts syndrome
    n1=en:smith-magenis syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  468. en:trichothiodystrophy --- r_associated #0: 37 --> en:roberts syndrome
    n1=en:trichothiodystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  469. faciès anormal, retard de croissance et retard mental --- r_associated #0: 37 --> en:roberts syndrome
    n1=faciès anormal, retard de croissance et retard mental | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  470. myocardiopathie de tako-tsubo --- r_associated #0: 37 --> en:roberts syndrome
    n1=myocardiopathie de tako-tsubo | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  471. van Bogaert (xanthomatose cérébrotendineuse de) --- r_associated #0: 37 --> en:roberts syndrome
    n1=van Bogaert (xanthomatose cérébrotendineuse de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=37
  472. communication interauriculaire --- r_associated #0: 36 --> en:roberts syndrome
    n1=communication interauriculaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  473. dysplasie ectodermique --- r_associated #0: 36 --> en:roberts syndrome
    n1=dysplasie ectodermique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  474. déficit en prolidase --- r_associated #0: 36 --> en:roberts syndrome
    n1=déficit en prolidase | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  475. ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) --- r_associated #0: 36 --> en:roberts syndrome
    n1=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  476. en:Gray platelet syndrome --- r_associated #0: 36 --> en:roberts syndrome
    n1=en:Gray platelet syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  477. en:Williams syndrome --- r_associated #0: 36 --> en:roberts syndrome
    n1=en:Williams syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  478. en:cerebral gigantism --- r_associated #0: 36 --> en:roberts syndrome
    n1=en:cerebral gigantism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  479. en:child's sudden death --- r_associated #0: 36 --> en:roberts syndrome
    n1=en:child's sudden death | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  480. en:craniofacial dysostosis --- r_associated #0: 36 --> en:roberts syndrome
    n1=en:craniofacial dysostosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  481. en:farber lipogranulomatosis --- r_associated #0: 36 --> en:roberts syndrome
    n1=en:farber lipogranulomatosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  482. en:hard skin syndrome parana type --- r_associated #0: 36 --> en:roberts syndrome
    n1=en:hard skin syndrome parana type | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  483. en:kallmann syndrome --- r_associated #0: 36 --> en:roberts syndrome
    n1=en:kallmann syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  484. en:microcephaly and chorioretinopathy, autosomal recessive, type 1 --- r_associated #0: 36 --> en:roberts syndrome
    n1=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  485. en:temporomandibular joint dysfunction syndrome --- r_associated #0: 36 --> en:roberts syndrome
    n1=en:temporomandibular joint dysfunction syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  486. hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle --- r_associated #0: 36 --> en:roberts syndrome
    n1=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  487. ichthyose --- r_associated #0: 36 --> en:roberts syndrome
    n1=ichthyose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  488. ichtyose, affection neurologique spastique, et oligophrénie --- r_associated #0: 36 --> en:roberts syndrome
    n1=ichtyose, affection neurologique spastique, et oligophrénie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  489. léproserie --- r_associated #0: 36 --> en:roberts syndrome
    n1=léproserie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  490. maladie à virus de Marburg --- r_associated #0: 36 --> en:roberts syndrome
    n1=maladie à virus de Marburg | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  491. porphyrie cutanée tardive --- r_associated #0: 36 --> en:roberts syndrome
    n1=porphyrie cutanée tardive | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  492. syndrome de bile épaisse --- r_associated #0: 36 --> en:roberts syndrome
    n1=syndrome de bile épaisse | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=36
  493. anasarque fœtoplacentaire --- r_associated #0: 35 --> en:roberts syndrome
    n1=anasarque fœtoplacentaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  494. cysticercose --- r_associated #0: 35 --> en:roberts syndrome
    n1=cysticercose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  495. cysticercose cérébrale --- r_associated #0: 35 --> en:roberts syndrome
    n1=cysticercose cérébrale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  496. cysticercose du système nerveux central --- r_associated #0: 35 --> en:roberts syndrome
    n1=cysticercose du système nerveux central | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  497. cysticercose neurologique --- r_associated #0: 35 --> en:roberts syndrome
    n1=cysticercose neurologique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  498. cysticercoses --- r_associated #0: 35 --> en:roberts syndrome
    n1=cysticercoses | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  499. dysplasie cléido-crânienne --- r_associated #0: 35 --> en:roberts syndrome
    n1=dysplasie cléido-crânienne | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  500. dysplasie cléidocrânienne --- r_associated #0: 35 --> en:roberts syndrome
    n1=dysplasie cléidocrânienne | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  501. dysplasie frontonasale --- r_associated #0: 35 --> en:roberts syndrome
    n1=dysplasie frontonasale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  502. en:acquired hyperostosis syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:acquired hyperostosis syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  503. en:albright's hereditary osteodystrophy --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:albright's hereditary osteodystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  504. en:beare-stevenson cutis gyrata syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:beare-stevenson cutis gyrata syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  505. en:caroli disease --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:caroli disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  506. en:choroideremia --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:choroideremia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  507. en:churg-strauss syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:churg-strauss syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  508. en:cleidocranial dysplasia --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:cleidocranial dysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  509. en:coffin-lowry syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:coffin-lowry syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  510. en:cogan-reese syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:cogan-reese syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  511. en:congenital amegakaryocytic thrombocytopenia --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:congenital amegakaryocytic thrombocytopenia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  512. en:congenital pain insensitivity --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:congenital pain insensitivity | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  513. en:conn syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:conn syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  514. en:connexin 26 gene anomaly --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:connexin 26 gene anomaly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  515. en:cysticercosis --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:cysticercosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  516. en:deafness, autosomal recessive 1a --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  517. en:digeorge syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:digeorge syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  518. en:dihydropyrimidine dehydrogenase deficiency --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:dihydropyrimidine dehydrogenase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  519. en:dravet syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:dravet syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  520. en:dry eye syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:dry eye syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  521. en:episodic pain syndrome, familial, 3 --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:episodic pain syndrome, familial, 3 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  522. en:frontonasal dysplasia --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:frontonasal dysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  523. en:hyperpipecolatemia --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:hyperpipecolatemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  524. en:hypohidrotic ectodermal dysplasia with immune deficiency --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:hypohidrotic ectodermal dysplasia with immune deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  525. en:inspissated bile syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:inspissated bile syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  526. en:juvenile x-linked retinoschisis --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:juvenile x-linked retinoschisis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  527. en:lupus anticoagulant disorder --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:lupus anticoagulant disorder | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  528. en:marshall syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:marshall syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  529. en:maternal diabetes and deafness syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:maternal diabetes and deafness syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  530. en:meconium aspiration syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:meconium aspiration syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  531. en:mental deficiency --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:mental deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  532. en:mild-severe postnatal growth deficiency --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:mild-severe postnatal growth deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  533. en:neurocysticercosis --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:neurocysticercosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  534. en:noonan syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:noonan syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  535. en:orofacial cleft 1 --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:orofacial cleft 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  536. en:pena-shokeir syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:pena-shokeir syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  537. en:penta x syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:penta x syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  538. en:prominent eyes --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:prominent eyes | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  539. en:pseudotrisomy 13 syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  540. en:severe intrauterine growth retardation --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:severe intrauterine growth retardation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  541. en:short rib-polydactyly syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:short rib-polydactyly syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  542. en:short stature homeobox deficiency --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:short stature homeobox deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  543. en:shprintzen-goldberg craniosynostosis syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:shprintzen-goldberg craniosynostosis syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  544. en:simpson golabi behmel syndrome type 1 --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:simpson golabi behmel syndrome type 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  545. en:sparse hair --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:sparse hair | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  546. en:syndrome of apparent mineralocorticoid excess --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:syndrome of apparent mineralocorticoid excess | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  547. en:treacher collins syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:treacher collins syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  548. en:uveomeningoencephalitic syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:uveomeningoencephalitic syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  549. en:variegate porphyria --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:variegate porphyria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  550. en:waterhouse-friderichsen syndrome --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:waterhouse-friderichsen syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  551. en:x-linked bulbar-muscular atrophy --- r_associated #0: 35 --> en:roberts syndrome
    n1=en:x-linked bulbar-muscular atrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  552. insensibilité congénitale à la douleur de type III --- r_associated #0: 35 --> en:roberts syndrome
    n1=insensibilité congénitale à la douleur de type III | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  553. maladie de Perthes --- r_associated #0: 35 --> en:roberts syndrome
    n1=maladie de Perthes | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  554. neurocysticercose --- r_associated #0: 35 --> en:roberts syndrome
    n1=neurocysticercose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  555. noma --- r_associated #0: 35 --> en:roberts syndrome
    n1=noma | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  556. syndrome de Sheehan --- r_associated #0: 35 --> en:roberts syndrome
    n1=syndrome de Sheehan | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  557. syndrome de plummer-vinson --- r_associated #0: 35 --> en:roberts syndrome
    n1=syndrome de plummer-vinson | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  558. trachéobronchomégalie --- r_associated #0: 35 --> en:roberts syndrome
    n1=trachéobronchomégalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  559. Syndrome de Marfan --- r_associated #0: 34 --> en:roberts syndrome
    n1=Syndrome de Marfan | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  560. en:17q21 microdeletion syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:17q21 microdeletion syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  561. en:Goltz syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:Goltz syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  562. en:Soto's syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:Soto's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  563. en:achard syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:achard syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  564. en:autoimmune polyendocrinopathy syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:autoimmune polyendocrinopathy syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  565. en:autoimmune polyglandular syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:autoimmune polyglandular syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  566. en:autoinflammatory syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:autoinflammatory syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  567. en:bicornuate uterus --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:bicornuate uterus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  568. en:birth length less than 40cm --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:birth length less than 40cm | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  569. en:blue sclera --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:blue sclera | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  570. en:byzanthine arch palate --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:byzanthine arch palate | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  571. en:cataplexia --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:cataplexia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  572. en:caused by mutation in the establishment of cohesion 1 homolog 2 gene (esco2, 609353.0001) --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:caused by mutation in the establishment of cohesion 1 homolog 2 gene (esco2, 609353.0001) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  573. en:charge syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:charge syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  574. en:complete trisomy 18 syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:complete trisomy 18 syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  575. en:d-glyceric aciduria --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:d-glyceric aciduria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  576. en:deletion 18q syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:deletion 18q syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  577. en:dentatorubral-pallidoluysian atrophy --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:dentatorubral-pallidoluysian atrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  578. en:drug hypersensitivity syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:drug hypersensitivity syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  579. en:ectrodactyly --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:ectrodactyly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  580. en:familial dysautonomia --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:familial dysautonomia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  581. en:glutaric aciduria, type 1 --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:glutaric aciduria, type 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  582. en:greig syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:greig syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  583. en:griscelli syndrome type 2 --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:griscelli syndrome type 2 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  584. en:hereditary angioedema --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:hereditary angioedema | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  585. en:hmg-coa lyase deficiency --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:hmg-coa lyase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  586. en:hymenolepiasis --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:hymenolepiasis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  587. en:ichthyosis --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:ichthyosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  588. en:leri-weill dyschondrosteosis --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:leri-weill dyschondrosteosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  589. en:liddle syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:liddle syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  590. en:lipase hypersecretion syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:lipase hypersecretion syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  591. en:lissencephaly --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:lissencephaly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  592. en:long-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:long-chain acyl-coa dehydrogenase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  593. en:malignant atrophic papulosis --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:malignant atrophic papulosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  594. en:malignant hyperthermia syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:malignant hyperthermia syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  595. en:maternal uniparental disomy chromosome 14 syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:maternal uniparental disomy chromosome 14 syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  596. en:meconium plug syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:meconium plug syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  597. en:mowat-wilson syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:mowat-wilson syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  598. en:myokymia --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:myokymia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  599. en:myositis --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:myositis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  600. en:myotonic disorder --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:myotonic disorder | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  601. en:neonatal progeroid syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:neonatal progeroid syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  602. en:neurological cysticercosis --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:neurological cysticercosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  603. en:neuropathy, hereditary sensory and autonomic, type vii --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:neuropathy, hereditary sensory and autonomic, type vii | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  604. en:non-trisomic autosomal aneuploidy --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:non-trisomic autosomal aneuploidy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  605. en:nuchal cystic hygroma --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:nuchal cystic hygroma | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  606. en:opitz g/bbb syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:opitz g/bbb syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  607. en:pentalogy of cantrell --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:pentalogy of cantrell | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  608. en:peritoneal panniculitis --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:peritoneal panniculitis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  609. en:persistent fetal circulation --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:persistent fetal circulation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  610. en:pettigrew syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:pettigrew syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  611. en:potter syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:potter syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  612. en:premature separation of centromeric heterochromatin --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:premature separation of centromeric heterochromatin | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  613. en:progressive bulbar palsy --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:progressive bulbar palsy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  614. en:pseudoachondroplasia --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:pseudoachondroplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  615. en:renal coloboma syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:renal coloboma syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  616. en:robinow syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:robinow syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  617. en:shallow orbits --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:shallow orbits | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  618. en:somnolence syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:somnolence syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  619. en:stevens-johnson syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:stevens-johnson syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  620. en:sudden unexplained infant death --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:sudden unexplained infant death | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  621. en:thyroid hormone resistance syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:thyroid hormone resistance syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  622. en:triple a syndrome --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:triple a syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  623. en:wilms tumor 1 gene syndromes --- r_associated #0: 34 --> en:roberts syndrome
    n1=en:wilms tumor 1 gene syndromes | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  624. hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale --- r_associated #0: 34 --> en:roberts syndrome
    n1=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  625. holoprosencéphalie familiale alobaire de type 1 --- r_associated #0: 34 --> en:roberts syndrome
    n1=holoprosencéphalie familiale alobaire de type 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  626. ichtyose folliculaire, atrichie et photophobie --- r_associated #0: 34 --> en:roberts syndrome
    n1=ichtyose folliculaire, atrichie et photophobie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  627. lissencéphalie --- r_associated #0: 34 --> en:roberts syndrome
    n1=lissencéphalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  628. onycho-patellaire (syndrome) --- r_associated #0: 34 --> en:roberts syndrome
    n1=onycho-patellaire (syndrome) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  629. ophtalmorhino-stomatoxérose --- r_associated #0: 34 --> en:roberts syndrome
    n1=ophtalmorhino-stomatoxérose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  630. pachyonychie congénitale de Jadassohn-Lewandowsky --- r_associated #0: 34 --> en:roberts syndrome
    n1=pachyonychie congénitale de Jadassohn-Lewandowsky | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  631. panencéphalite subaiguë sclérosante --- r_associated #0: 34 --> en:roberts syndrome
    n1=panencéphalite subaiguë sclérosante | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  632. papulose atrophiante maligne de Degos --- r_associated #0: 34 --> en:roberts syndrome
    n1=papulose atrophiante maligne de Degos | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  633. trisomie --- r_associated #0: 34 --> en:roberts syndrome
    n1=trisomie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=34
  634. en:feeble-mindedness --- r_associated #0: 33 --> en:roberts syndrome
    n1=en:feeble-mindedness | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=33
  635. en:marburg virus disease --- r_associated #0: 33 --> en:roberts syndrome
    n1=en:marburg virus disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=33
  636. en:porphyria cutanea tarda --- r_associated #0: 33 --> en:roberts syndrome
    n1=en:porphyria cutanea tarda | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=33
  637. en:prolidase deficiency --- r_associated #0: 33 --> en:roberts syndrome
    n1=en:prolidase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=33
  638. en:takotsubo cardiomyopathy --- r_associated #0: 33 --> en:roberts syndrome
    n1=en:takotsubo cardiomyopathy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=33
  639. mésentérique supérieure (syndrome de l'artère) --- r_associated #0: 33 --> en:roberts syndrome
    n1=mésentérique supérieure (syndrome de l'artère) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=33
  640. syndrome métabolique --- r_associated #0: 33 --> en:roberts syndrome
    n1=syndrome métabolique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=33
  641. Seitelberger (maladie de) --- r_associated #0: 32 --> en:roberts syndrome
    n1=Seitelberger (maladie de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  642. alvéolite --- r_associated #0: 32 --> en:roberts syndrome
    n1=alvéolite | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  643. dentinogénèse imparfaite --- r_associated #0: 32 --> en:roberts syndrome
    n1=dentinogénèse imparfaite | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  644. dysostose crâniofaciale --- r_associated #0: 32 --> en:roberts syndrome
    n1=dysostose crâniofaciale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  645. en:22q telomere deletion syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:22q telomere deletion syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  646. en:Marfan's disease --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:Marfan's disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  647. en:abnormality of the pinna --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:abnormality of the pinna | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  648. en:acrodysostosis 1 --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:acrodysostosis 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  649. en:adenine phosphoribosyltransferase deficiency --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:adenine phosphoribosyltransferase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  650. en:alagille syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:alagille syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  651. en:alkaptonuria --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:alkaptonuria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  652. en:allan-herndon-dudley syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:allan-herndon-dudley syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  653. en:alpha-1 antitrypsin deficiency --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:alpha-1 antitrypsin deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  654. en:argininemia --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:argininemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  655. en:argininosuccinic aciduria --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:argininosuccinic aciduria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  656. en:arnold-chiari deformity --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:arnold-chiari deformity | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  657. en:atrophic muscular disorder --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:atrophic muscular disorder | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  658. en:autosomal dominant congenital deafness with onychodystrophy --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:autosomal dominant congenital deafness with onychodystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  659. en:bernard-soulier syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:bernard-soulier syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  660. en:bile acid synthesis defect --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:bile acid synthesis defect | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  661. en:biotinidase deficiency --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:biotinidase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  662. en:brachycephalies --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:brachycephalies | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  663. en:brain iron accumulation type i syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:brain iron accumulation type i syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  664. en:burning mouth syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:burning mouth syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  665. en:carbonic anhydrase i deficiency --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:carbonic anhydrase i deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  666. en:chromosome 16p12.1 deletion syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:chromosome 16p12.1 deletion syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  667. en:combined lipase deficiency --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:combined lipase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  668. en:congenital structural myopathy --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:congenital structural myopathy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  669. en:cryptophthalmos syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:cryptophthalmos syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  670. en:deletion 18p syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:deletion 18p syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  671. en:donohue syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:donohue syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  672. en:drug- and toxin-induced pulmonary arterial hypertension --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:drug- and toxin-induced pulmonary arterial hypertension | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  673. en:dysfunctional elimination syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:dysfunctional elimination syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  674. en:enlarged labia minora --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:enlarged labia minora | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  675. en:familial hypertrophic cardiomyopathy --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:familial hypertrophic cardiomyopathy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  676. en:familial partial lipodystrophy --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:familial partial lipodystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  677. en:fetal hydantoin syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:fetal hydantoin syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  678. en:fibrodysplasia ossificans progressiva --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:fibrodysplasia ossificans progressiva | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  679. en:fisher syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:fisher syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  680. en:gangrenous stomatitis --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:gangrenous stomatitis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  681. en:gray platelet syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:gray platelet syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  682. en:hallermann syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:hallermann syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  683. en:hereditary hyperbilirubinemia --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:hereditary hyperbilirubinemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  684. en:hermansky-pudlak syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:hermansky-pudlak syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  685. en:infantile convulsions and paroxysmal choreoathetosis, familial --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:infantile convulsions and paroxysmal choreoathetosis, familial | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  686. en:jackson-weiss syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:jackson-weiss syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  687. en:lethal multiple pterygium syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:lethal multiple pterygium syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  688. en:leucinosis --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:leucinosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  689. en:levocardia --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:levocardia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  690. en:lubs x-linked mental retardation syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:lubs x-linked mental retardation syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  691. en:menkes disease --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:menkes disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  692. en:mental retardation, autosomal dominant 9 --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:mental retardation, autosomal dominant 9 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  693. en:metabolic syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:metabolic syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  694. en:narrow naris --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:narrow naris | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  695. en:orofaciodigital syndrome type 6 --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:orofaciodigital syndrome type 6 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  696. en:osteopoikilosis --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:osteopoikilosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  697. en:papillon-lefevre syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:papillon-lefevre syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  698. en:periodic fever syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:periodic fever syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  699. en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  700. en:rieger syndrome type 1 --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:rieger syndrome type 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  701. en:sanfilippo syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:sanfilippo syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  702. en:systemic inflammatory response syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:systemic inflammatory response syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  703. en:telecanthus --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:telecanthus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  704. en:thrombocytopenia 2 --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:thrombocytopenia 2 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  705. en:vertebral artery syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:vertebral artery syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  706. en:wernicke-korsakoff syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:wernicke-korsakoff syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  707. en:wide nasal bridge --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:wide nasal bridge | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  708. en:wolf-hirschhorn syndrome --- r_associated #0: 32 --> en:roberts syndrome
    n1=en:wolf-hirschhorn syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  709. nanisme, retard mental, anomalies oculaires --- r_associated #0: 32 --> en:roberts syndrome
    n1=nanisme, retard mental, anomalies oculaires | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  710. neuropathie optique --- r_associated #0: 32 --> en:roberts syndrome
    n1=neuropathie optique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  711. syndrome inflammatoire aigu systémique --- r_associated #0: 32 --> en:roberts syndrome
    n1=syndrome inflammatoire aigu systémique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=32
  712. TPN ou NADP --- r_associated #0: 31 --> en:roberts syndrome
    n1=TPN ou NADP | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  713. anasarque --- r_associated #0: 31 --> en:roberts syndrome
    n1=anasarque | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  714. dysplasie campomélique --- r_associated #0: 31 --> en:roberts syndrome
    n1=dysplasie campomélique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  715. en:behcet syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:behcet syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  716. en:chromosome 2q37 deletion syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:chromosome 2q37 deletion syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  717. en:complete trisomy 13 syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:complete trisomy 13 syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  718. en:cortical dysplasia-focal epilepsy syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:cortical dysplasia-focal epilepsy syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  719. en:craniofacial abnormalities --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:craniofacial abnormalities | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  720. en:de toni-debre-fanconi syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:de toni-debre-fanconi syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  721. en:dumping stomach --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:dumping stomach | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  722. en:dyschromatosis symmetrica hereditaria --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:dyschromatosis symmetrica hereditaria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  723. en:ellis-van creveld syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:ellis-van creveld syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  724. en:endocrine syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:endocrine syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  725. en:erythropoietic porphyria --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:erythropoietic porphyria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  726. en:esco2 gene --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:esco2 gene | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  727. en:esco2, arg169ter --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:esco2, arg169ter | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  728. en:feingold syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:feingold syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  729. en:gitelman syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:gitelman syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  730. en:goldenhar syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:goldenhar syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  731. en:hereditary mucosal leukokeratosis --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:hereditary mucosal leukokeratosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  732. en:holocarboxylase synthetase deficiency --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:holocarboxylase synthetase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  733. en:holt-oram syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:holt-oram syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  734. en:hypertrophy of clitoris --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:hypertrophy of clitoris | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  735. en:immunodeficiency with hyper-igm type 2 --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:immunodeficiency with hyper-igm type 2 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  736. en:insulin receptor mutation - associated insulin resistance syndromes --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:insulin receptor mutation - associated insulin resistance syndromes | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  737. en:karyotype analysis normal finding --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:karyotype analysis normal finding | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  738. en:kimura disease --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:kimura disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  739. en:lig4 syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:lig4 syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  740. en:malabsorption syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:malabsorption syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  741. en:micrognathia --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:micrognathia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  742. en:mucolipidosis type iii gamma --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:mucolipidosis type iii gamma | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  743. en:myhre syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:myhre syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  744. en:nail-patella syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:nail-patella syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  745. en:neoplastic syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:neoplastic syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  746. en:nephrocalcinosis --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:nephrocalcinosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  747. en:netherton syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:netherton syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  748. en:ossification of posterior longitudinal ligament --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:ossification of posterior longitudinal ligament | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  749. en:pain agnosia --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:pain agnosia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  750. en:panuveitis --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:panuveitis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  751. en:pearson marrow-pancreas syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:pearson marrow-pancreas syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  752. en:perthes disease --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:perthes disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  753. en:pyramidal tract dysfunction --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:pyramidal tract dysfunction | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  754. en:reduction in number of toes --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:reduction in number of toes | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  755. en:reversible posterior leukoencephalopathy syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:reversible posterior leukoencephalopathy syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  756. en:rudimentary gallbladder --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:rudimentary gallbladder | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  757. en:schwartz-jampel syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:schwartz-jampel syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  758. en:situs inversus viscerum --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:situs inversus viscerum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  759. en:sjogren-larsson syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:sjogren-larsson syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  760. en:stein-leventhal syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:stein-leventhal syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  761. en:subacute sclerosing panencephalitis --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:subacute sclerosing panencephalitis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  762. en:tissue kallikrein deficiency --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:tissue kallikrein deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  763. en:townes-brocks syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:townes-brocks syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  764. en:tubulointerstitial nephritis and uveitis --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:tubulointerstitial nephritis and uveitis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  765. en:wolfram syndrome --- r_associated #0: 31 --> en:roberts syndrome
    n1=en:wolfram syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  766. hydramnios --- r_associated #0: 31 --> en:roberts syndrome
    n1=hydramnios | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  767. lipodystrophie partielle familiale --- r_associated #0: 31 --> en:roberts syndrome
    n1=lipodystrophie partielle familiale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  768. lévocardie --- r_associated #0: 31 --> en:roberts syndrome
    n1=lévocardie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  769. myokymie --- r_associated #0: 31 --> en:roberts syndrome
    n1=myokymie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  770. myosite --- r_associated #0: 31 --> en:roberts syndrome
    n1=myosite | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  771. myosites --- r_associated #0: 31 --> en:roberts syndrome
    n1=myosites | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  772. néphrocalcinose --- r_associated #0: 31 --> en:roberts syndrome
    n1=néphrocalcinose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  773. oligophrénie --- r_associated #0: 31 --> en:roberts syndrome
    n1=oligophrénie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  774. onycho-ostéodysostose --- r_associated #0: 31 --> en:roberts syndrome
    n1=onycho-ostéodysostose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  775. ostéopoecilie --- r_associated #0: 31 --> en:roberts syndrome
    n1=ostéopoecilie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  776. panuvéite --- r_associated #0: 31 --> en:roberts syndrome
    n1=panuvéite | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  777. pemphigoïde bénigne des muqueuses --- r_associated #0: 31 --> en:roberts syndrome
    n1=pemphigoïde bénigne des muqueuses | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  778. porphyrie érythropoïétique --- r_associated #0: 31 --> en:roberts syndrome
    n1=porphyrie érythropoïétique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  779. syndrome de Martin-Bell --- r_associated #0: 31 --> en:roberts syndrome
    n1=syndrome de Martin-Bell | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  780. syndrome de malabsorption --- r_associated #0: 31 --> en:roberts syndrome
    n1=syndrome de malabsorption | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=31
  781. Syndrome d'Alagille --- r_associated #0: 30 --> en:roberts syndrome
    n1=Syndrome d'Alagille | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  782. acrodermatite entéropathique --- r_associated #0: 30 --> en:roberts syndrome
    n1=acrodermatite entéropathique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  783. anomalie du septum auriculaire --- r_associated #0: 30 --> en:roberts syndrome
    n1=anomalie du septum auriculaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  784. arriération --- r_associated #0: 30 --> en:roberts syndrome
    n1=arriération | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  785. détresse respiratoire --- r_associated #0: 30 --> en:roberts syndrome
    n1=détresse respiratoire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  786. en:Alice in wonderland Syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:Alice in wonderland Syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  787. en:Dercum's disease --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:Dercum's disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  788. en:FPLD --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:FPLD | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  789. en:Seitelberger's neuroaxonal dystrophy --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:Seitelberger's neuroaxonal dystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  790. en:Stargardt disease --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:Stargardt disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  791. en:Townes-Brocks syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:Townes-Brocks syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  792. en:Waterhouse-Friderichsen syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:Waterhouse-Friderichsen syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  793. en:acrocallosal syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:acrocallosal syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  794. en:acrodermatitis --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:acrodermatitis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  795. en:acrodermatitis enteropathica --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:acrodermatitis enteropathica | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  796. en:aicardi syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:aicardi syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  797. en:alligator skin --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:alligator skin | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  798. en:aniridia --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:aniridia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  799. en:arakawa syndrome ii --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:arakawa syndrome ii | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  800. en:atrial septal defect --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:atrial septal defect | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  801. en:atypical hemolytic uremic syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:atypical hemolytic uremic syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  802. en:autosomal dominant optic atrophy --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:autosomal dominant optic atrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  803. en:cadasil syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:cadasil syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  804. en:cleft lip and palate --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:cleft lip and palate | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  805. en:codas syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:codas syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  806. en:complex regional pain syndrome i --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:complex regional pain syndrome i | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  807. en:congenital cortical hyperostosis --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:congenital cortical hyperostosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  808. en:craniostenosis --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:craniostenosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  809. en:familial atypical hemolytic uremic syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:familial atypical hemolytic uremic syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  810. en:fetal retinoid syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:fetal retinoid syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  811. en:fox-fordyce disease --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:fox-fordyce disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  812. en:glanzmann thrombasthenia --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:glanzmann thrombasthenia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  813. en:glycogen storage disease --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:glycogen storage disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  814. en:gray baby syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:gray baby syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  815. en:holmes-adie syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:holmes-adie syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  816. en:hunter syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:hunter syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  817. en:hyperlysinemia --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:hyperlysinemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  818. en:hypoxaemia --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:hypoxaemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  819. en:ichthyosis vera --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:ichthyosis vera | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  820. en:insufficient breast milk syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:insufficient breast milk syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  821. en:juvenile cataract --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:juvenile cataract | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  822. en:kshv inflammatory cytokine syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:kshv inflammatory cytokine syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  823. en:learning disability --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:learning disability | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  824. en:mental dullness --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:mental dullness | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  825. en:mental handicap --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:mental handicap | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  826. en:mitochondrial dna depletion syndrome 12 --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:mitochondrial dna depletion syndrome 12 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  827. en:odontogenesis imperfecta --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:odontogenesis imperfecta | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  828. en:overgrowth syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:overgrowth syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  829. en:plasma kallikrein deficiency --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:plasma kallikrein deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  830. en:potocki-shaffer syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:potocki-shaffer syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  831. en:proctatresia --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:proctatresia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  832. en:respiratory distress --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:respiratory distress | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  833. en:respiratory distress syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:respiratory distress syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  834. en:retardation --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:retardation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  835. en:sandifer's syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:sandifer's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  836. en:sick euthyroid syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:sick euthyroid syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  837. en:sids --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:sids | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  838. en:sudden unexplained death in childhood --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:sudden unexplained death in childhood | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  839. en:sunset syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:sunset syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  840. en:triploidy syndrome --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:triploidy syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  841. en:trisomy --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:trisomy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  842. en:urea cycle metabolism disorder --- r_associated #0: 30 --> en:roberts syndrome
    n1=en:urea cycle metabolism disorder | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  843. inflammation musculaire --- r_associated #0: 30 --> en:roberts syndrome
    n1=inflammation musculaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  844. maladie de Tay-Sachs --- r_associated #0: 30 --> en:roberts syndrome
    n1=maladie de Tay-Sachs | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  845. maladie de hurler --- r_associated #0: 30 --> en:roberts syndrome
    n1=maladie de hurler | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  846. microdélétion 5q35 --- r_associated #0: 30 --> en:roberts syndrome
    n1=microdélétion 5q35 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  847. présentation sacro-iliaque droite antérieure --- r_associated #0: 30 --> en:roberts syndrome
    n1=présentation sacro-iliaque droite antérieure | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  848. syndrome de Zellweger --- r_associated #0: 30 --> en:roberts syndrome
    n1=syndrome de Zellweger | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  849. syndrome de détresse respiratoire --- r_associated #0: 30 --> en:roberts syndrome
    n1=syndrome de détresse respiratoire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  850. syndrome de li-fraumeni --- r_associated #0: 30 --> en:roberts syndrome
    n1=syndrome de li-fraumeni | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  851. syndrome du bébé gris --- r_associated #0: 30 --> en:roberts syndrome
    n1=syndrome du bébé gris | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  852. syndrome gris du nourrisson --- r_associated #0: 30 --> en:roberts syndrome
    n1=syndrome gris du nourrisson | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  853. syndrome hémolytique et urémique atypique --- r_associated #0: 30 --> en:roberts syndrome
    n1=syndrome hémolytique et urémique atypique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
  854. choc toxique --- r_associated #0: 29 --> en:roberts syndrome
    n1=choc toxique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  855. cholestase intrahépatique progressive familiale de type 1 --- r_associated #0: 29 --> en:roberts syndrome
    n1=cholestase intrahépatique progressive familiale de type 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  856. cholestases intrahépatiques progressives familiales --- r_associated #0: 29 --> en:roberts syndrome
    n1=cholestases intrahépatiques progressives familiales | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  857. cétoacidurie à chaînes ramifiées --- r_associated #0: 29 --> en:roberts syndrome
    n1=cétoacidurie à chaînes ramifiées | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  858. en:CDA --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:CDA | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  859. en:Fox-Fordyce disease --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:Fox-Fordyce disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  860. en:Hebra's pityriasis --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:Hebra's pityriasis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  861. en:Marburg virus disease --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:Marburg virus disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  862. en:acatalasemia --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:acatalasemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  863. en:aids --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:aids | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  864. en:anal imperforation --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:anal imperforation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  865. en:bonnevie-ullrich syndrome --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:bonnevie-ullrich syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  866. en:carnitine palmitoyltransferase i deficiency --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:carnitine palmitoyltransferase i deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  867. en:cerebellar atrophy --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:cerebellar atrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  868. en:darier disease --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:darier disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  869. en:deafness, autosomal recessive 49 --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:deafness, autosomal recessive 49 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  870. en:escobar syndrome --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:escobar syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  871. en:fatal familial insomnia --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:fatal familial insomnia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  872. en:fish skin disease --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:fish skin disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  873. en:gerstmann-straussler-scheinker disease --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:gerstmann-straussler-scheinker disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  874. en:hand and foot deformity --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:hand and foot deformity | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  875. en:hansenarium --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:hansenarium | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  876. en:hereditary coproporphyria --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:hereditary coproporphyria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  877. en:hereditary persistence of fetal hemoglobin --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:hereditary persistence of fetal hemoglobin | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  878. en:heritable pulmonary arterial hypertension --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:heritable pulmonary arterial hypertension | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  879. en:high molecular weight kininogen deficiency --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:high molecular weight kininogen deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  880. en:horner syndrome --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:horner syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  881. en:idiopathic hypersomnolence --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:idiopathic hypersomnolence | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  882. en:kabuki syndrome --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:kabuki syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  883. en:leriche syndrome --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:leriche syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  884. en:lesch-nyhan syndrome --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:lesch-nyhan syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  885. en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  886. en:malar flattening --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:malar flattening | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  887. en:miller-dieker syndrome --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:miller-dieker syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  888. en:mitochondrial neurogastrointestingal encephalopathy --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:mitochondrial neurogastrointestingal encephalopathy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  889. en:palmar-plantar erythodysthesia --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:palmar-plantar erythodysthesia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  890. en:polycystic kidney - body part --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:polycystic kidney - body part | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  891. en:pseudotumor cerebri --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:pseudotumor cerebri | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  892. en:spondyloepimetaphyseal dysplasia with joint laxity type 2 --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:spondyloepimetaphyseal dysplasia with joint laxity type 2 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  893. en:stargardt disease --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:stargardt disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  894. en:surfactant protein deficiency --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:surfactant protein deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  895. en:trisomy 14 mosaicism --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:trisomy 14 mosaicism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  896. en:twiddler's syndrome --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:twiddler's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  897. en:xerophtalmy --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:xerophtalmy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  898. en:xxxy and xxxxy syndrome --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:xxxy and xxxxy syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  899. en:yellow nail --- r_associated #0: 29 --> en:roberts syndrome
    n1=en:yellow nail | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  900. fibromyalgie --- r_associated #0: 29 --> en:roberts syndrome
    n1=fibromyalgie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  901. maladie de dubin-johnson --- r_associated #0: 29 --> en:roberts syndrome
    n1=maladie de dubin-johnson | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  902. maladie du cri du chat --- r_associated #0: 29 --> en:roberts syndrome
    n1=maladie du cri du chat | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  903. pemphigus bénin des muqueuses --- r_associated #0: 29 --> en:roberts syndrome
    n1=pemphigus bénin des muqueuses | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  904. porphyrie (anesthésie chez un patient atteint de) --- r_associated #0: 29 --> en:roberts syndrome
    n1=porphyrie (anesthésie chez un patient atteint de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  905. syndrome de Williams --- r_associated #0: 29 --> en:roberts syndrome
    n1=syndrome de Williams | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  906. syndrome de membrane hyaline --- r_associated #0: 29 --> en:roberts syndrome
    n1=syndrome de membrane hyaline | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=29
  907. DUGV --- r_associated #0: 28 --> en:roberts syndrome
    n1=DUGV | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  908. Maladie de Tay-Sachs --- r_associated #0: 28 --> en:roberts syndrome
    n1=Maladie de Tay-Sachs | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  909. albinisme oculocutané de type mutant jaune --- r_associated #0: 28 --> en:roberts syndrome
    n1=albinisme oculocutané de type mutant jaune | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  910. atransferrinémie --- r_associated #0: 28 --> en:roberts syndrome
    n1=atransferrinémie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  911. déficit congénital en mégacaryocytes --- r_associated #0: 28 --> en:roberts syndrome
    n1=déficit congénital en mégacaryocytes | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  912. en:5 alpha steroid reductase 2 deficiency --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:5 alpha steroid reductase 2 deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  913. en:Alagille's syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:Alagille's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  914. en:allgrove syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:allgrove syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  915. en:alpha-methylacyl-coa racemase deficiency --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:alpha-methylacyl-coa racemase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  916. en:and mental retardation --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:and mental retardation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  917. en:anhidrotic ectodermal dysplasia 1 --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:anhidrotic ectodermal dysplasia 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  918. en:arrhythmogenic right ventricular dysplasia --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:arrhythmogenic right ventricular dysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  919. en:auditory perceptual disorder --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:auditory perceptual disorder | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  920. en:bardet-biedl syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:bardet-biedl syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  921. en:blau syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:blau syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  922. en:calciphylaxis --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:calciphylaxis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  923. en:cockayne syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:cockayne syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  924. en:congenital bilateral aplasia of the vas deferens --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:congenital bilateral aplasia of the vas deferens | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  925. en:congenital disorder of deglycosylation --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:congenital disorder of deglycosylation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  926. en:congenital fiber-type disproportion --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:congenital fiber-type disproportion | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  927. en:congenital malformation syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:congenital malformation syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  928. en:crigler-najjar syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:crigler-najjar syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  929. en:deafness, autosomal recessive 28 --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:deafness, autosomal recessive 28 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  930. en:empty sella syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:empty sella syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  931. en:fibromyalgia --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:fibromyalgia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  932. en:fragile x tremor/ataxia syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:fragile x tremor/ataxia syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  933. en:frohlich syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:frohlich syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  934. en:gargoylism --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:gargoylism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  935. en:heterotaxy syndrome with asplenia --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:heterotaxy syndrome with asplenia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  936. en:hyaline membrane syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:hyaline membrane syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  937. en:jervell and lange nielsen syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:jervell and lange nielsen syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  938. en:kenny-caffey syndrome type 2 --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:kenny-caffey syndrome type 2 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  939. en:kleine-levin syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:kleine-levin syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  940. en:likely allelic to sc phocomelia syndrome (269000) --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:likely allelic to sc phocomelia syndrome (269000) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  941. en:mallory-weiss syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:mallory-weiss syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  942. en:meesmann corneal dystrophy --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:meesmann corneal dystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  943. en:microphthalmos --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:microphthalmos | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  944. en:multiple vascular disruption syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:multiple vascular disruption syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  945. en:n-acetylglutamate synthase deficiency --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:n-acetylglutamate synthase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  946. en:neuronal intranuclear inclusion disease --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:neuronal intranuclear inclusion disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  947. en:obstructive sleep apnea syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:obstructive sleep apnea syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  948. en:poland syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:poland syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  949. en:progressive familial intrahepatic cholestasis --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:progressive familial intrahepatic cholestasis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  950. en:pyruvate dehydrogenase deficiency --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:pyruvate dehydrogenase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  951. en:restless leg syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:restless leg syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  952. en:silvery blonde scalp hair --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:silvery blonde scalp hair | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  953. en:togaviridae infection --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:togaviridae infection | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  954. en:tolosa-hunt syndrome --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:tolosa-hunt syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  955. en:underdeveloped nasal alae --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:underdeveloped nasal alae | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  956. en:vacterl association --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:vacterl association | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  957. en:wegener granulomatosis --- r_associated #0: 28 --> en:roberts syndrome
    n1=en:wegener granulomatosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  958. glycogénose --- r_associated #0: 28 --> en:roberts syndrome
    n1=glycogénose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  959. hémicéphalie --- r_associated #0: 28 --> en:roberts syndrome
    n1=hémicéphalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  960. maladie de dercum --- r_associated #0: 28 --> en:roberts syndrome
    n1=maladie de dercum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  961. odontogénèse imparfaite --- r_associated #0: 28 --> en:roberts syndrome
    n1=odontogénèse imparfaite | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=28
  962. Marfan (maladie de) --- r_associated #0: 27 --> en:roberts syndrome
    n1=Marfan (maladie de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  963. albinisme --- r_associated #0: 27 --> en:roberts syndrome
    n1=albinisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  964. cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie --- r_associated #0: 27 --> en:roberts syndrome
    n1=cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  965. choc toxique staphylococcique --- r_associated #0: 27 --> en:roberts syndrome
    n1=choc toxique staphylococcique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  966. déficit en biotinidase --- r_associated #0: 27 --> en:roberts syndrome
    n1=déficit en biotinidase | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  967. dégénérescence wallérienne --- r_associated #0: 27 --> en:roberts syndrome
    n1=dégénérescence wallérienne | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  968. en:10p13-p14 deletion syndrome --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:10p13-p14 deletion syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  969. en:Degos's syndrome --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:Degos's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  970. en:achondrogenesis --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:achondrogenesis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  971. en:albinism --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:albinism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  972. en:amyoplasia congenita --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:amyoplasia congenita | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  973. en:barth syndrome --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:barth syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  974. en:campomelic dysplasia --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:campomelic dysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  975. en:chilblains --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:chilblains | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  976. en:chromosome 15q11-q13 duplication syndrome --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:chromosome 15q11-q13 duplication syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  977. en:complex regional pain syndrome ii --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:complex regional pain syndrome ii | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  978. en:cranial nerve palsy --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:cranial nerve palsy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  979. en:cri du chat syndrome --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:cri du chat syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  980. en:eiken type chondrodysplasia --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:eiken type chondrodysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  981. en:esco2, 1-bp ins, 750g --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:esco2, 1-bp ins, 750g | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  982. en:exomphalos --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:exomphalos | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  983. en:fusion of metacarpal bones --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:fusion of metacarpal bones | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  984. en:hereditary orotic aciduria --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:hereditary orotic aciduria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  985. en:hydrocephalus --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:hydrocephalus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  986. en:hyperviscosity syndrome --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:hyperviscosity syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  987. en:leigh disease --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:leigh disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  988. en:leprosary --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:leprosary | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  989. en:mental retardation, autosomal recessive 34 --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:mental retardation, autosomal recessive 34 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  990. en:methionine adenosyltransferase deficiency --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:methionine adenosyltransferase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  991. en:morosis --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:morosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  992. en:mullerian inhibiting factor deficiency --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:mullerian inhibiting factor deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  993. en:mullerian-renal-cervical spine syndrome --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:mullerian-renal-cervical spine syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  994. en:nelson syndrome --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:nelson syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  995. en:neural tube defect --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:neural tube defect | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  996. en:neurotoxicity syndrome --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:neurotoxicity syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  997. en:pierre robin syndrome --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:pierre robin syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  998. en:rhizomelic dysplasia --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:rhizomelic dysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  999. en:scheie syndrome --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:scheie syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  1000. en:schinzel-giedion midface-retraction syndrome --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:schinzel-giedion midface-retraction syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  1001. en:selective antibody deficiency with normal immunoglobulins --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:selective antibody deficiency with normal immunoglobulins | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  1002. en:single central incisor syndrome --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:single central incisor syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  1003. en:synpolydactyly --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:synpolydactyly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  1004. en:tempi syndrome --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:tempi syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  1005. en:x-linked dominant hypophosphatemic rickets --- r_associated #0: 27 --> en:roberts syndrome
    n1=en:x-linked dominant hypophosphatemic rickets | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  1006. fragilité osseuse avec craniosynostose, exophtalmie, hydrocéphalie et faciès caractéristique --- r_associated #0: 27 --> en:roberts syndrome
    n1=fragilité osseuse avec craniosynostose, exophtalmie, hydrocéphalie et faciès caractéristique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  1007. lichen ruber acuminatus --- r_associated #0: 27 --> en:roberts syndrome
    n1=lichen ruber acuminatus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  1008. syndrome de Li-Fraumeni --- r_associated #0: 27 --> en:roberts syndrome
    n1=syndrome de Li-Fraumeni | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=27
  1009. Duane (syndrome de) --- r_associated #0: 26 --> en:roberts syndrome
    n1=Duane (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1010. Jacobsen (syndrome de) --- r_associated #0: 26 --> en:roberts syndrome
    n1=Jacobsen (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1011. Kawasaki (maladie de) --- r_associated #0: 26 --> en:roberts syndrome
    n1=Kawasaki (maladie de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1012. acromégalie, plis cutanés de la face et du cuir chevelu, et leucomes cornéens --- r_associated #0: 26 --> en:roberts syndrome
    n1=acromégalie, plis cutanés de la face et du cuir chevelu, et leucomes cornéens | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1013. aniridie, ataxie cérébelleuse et déficience mentale --- r_associated #0: 26 --> en:roberts syndrome
    n1=aniridie, ataxie cérébelleuse et déficience mentale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1014. anomalie d'Ebstein --- r_associated #0: 26 --> en:roberts syndrome
    n1=anomalie d'Ebstein | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1015. dextrocardie --- r_associated #0: 26 --> en:roberts syndrome
    n1=dextrocardie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1016. distomatoses pulmonaires --- r_associated #0: 26 --> en:roberts syndrome
    n1=distomatoses pulmonaires | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1017. dysérythropoïèse congénitale --- r_associated #0: 26 --> en:roberts syndrome
    n1=dysérythropoïèse congénitale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1018. déficience mentale --- r_associated #0: 26 --> en:roberts syndrome
    n1=déficience mentale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1019. en:Gitelman syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:Gitelman syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1020. en:Günther's disease --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:Günther's disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1021. en:Leriche syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:Leriche syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1022. en:Seitelberger's disease --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:Seitelberger's disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1023. en:anaerosis --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:anaerosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1024. en:anti-AIDS --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:anti-AIDS | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1025. en:atransferrinemia --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:atransferrinemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1026. en:autosomal recessive hypohidrotic ectodermal dysplasia --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:autosomal recessive hypohidrotic ectodermal dysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1027. en:cafe au lait spots on trunk and extremities --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:cafe au lait spots on trunk and extremities | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1028. en:cerebrooculofacioskeletal syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:cerebrooculofacioskeletal syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1029. en:chromosome 16p11.2 deletion syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:chromosome 16p11.2 deletion syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1030. en:chronic infantile neurological cutaneous and articular syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:chronic infantile neurological cutaneous and articular syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1031. en:coloboma and anal atresia syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:coloboma and anal atresia syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1032. en:compartment syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:compartment syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1033. en:congenital dyserythropoietic anemia --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:congenital dyserythropoietic anemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1034. en:cor triatriatum --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:cor triatriatum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1035. en:cysticercus disease --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:cysticercus disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1036. en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1037. en:dextrocardia --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:dextrocardia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1038. en:double cortex syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:double cortex syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1039. en:ebstein anomaly --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:ebstein anomaly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1040. en:esco2, trp539gly --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:esco2, trp539gly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1041. en:factor v leiden --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:factor v leiden | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1042. en:failure of the mind --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:failure of the mind | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1043. en:generalized arterial calcification of infancy 1 --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:generalized arterial calcification of infancy 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1044. en:glucose-6-phosphate dehydrogenase deficiency --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:glucose-6-phosphate dehydrogenase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1045. en:glutaric aciduria type 1 --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:glutaric aciduria type 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1046. en:hantavirus pulmonary syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:hantavirus pulmonary syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1047. en:hartnup disease --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:hartnup disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1048. en:hypothalamic hamartoblastoma --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:hypothalamic hamartoblastoma | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1049. en:laurence-moon syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:laurence-moon syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1050. en:leopard syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:leopard syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1051. en:lethal neonatal rigidity and multifocal seizure syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:lethal neonatal rigidity and multifocal seizure syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1052. en:melas syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:melas syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1053. en:monosomy 13q syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:monosomy 13q syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1054. en:neuroacanthocytosis --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:neuroacanthocytosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1055. en:norrie syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:norrie syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1056. en:oligergasia --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:oligergasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1057. en:osteopoecilia --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:osteopoecilia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1058. en:paragonimiasis --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:paragonimiasis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1059. en:pelizaeus-merzbacher disease --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:pelizaeus-merzbacher disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1060. en:primary carnitine deficiency --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:primary carnitine deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1061. en:prune belly syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:prune belly syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1062. en:thyroid dysgenesis --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:thyroid dysgenesis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1063. en:vitelliform macular dystrophy --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:vitelliform macular dystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1064. en:von hippel-lindau syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:von hippel-lindau syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1065. en:waardenburg syndrome --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:waardenburg syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1066. en:with growth retardation --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:with growth retardation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1067. en:x-linked creatine transporter deficiency --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:x-linked creatine transporter deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1068. en:xerophthalmia --- r_associated #0: 26 --> en:roberts syndrome
    n1=en:xerophthalmia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1069. malformation d'Ebstein --- r_associated #0: 26 --> en:roberts syndrome
    n1=malformation d'Ebstein | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1070. neuro-acanthocytose --- r_associated #0: 26 --> en:roberts syndrome
    n1=neuro-acanthocytose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1071. paragonimiase --- r_associated #0: 26 --> en:roberts syndrome
    n1=paragonimiase | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1072. paragonimose --- r_associated #0: 26 --> en:roberts syndrome
    n1=paragonimose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1073. psychose de Korsakoff --- r_associated #0: 26 --> en:roberts syndrome
    n1=psychose de Korsakoff | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1074. syndrome cérébro-oculo-faciosquelettique --- r_associated #0: 26 --> en:roberts syndrome
    n1=syndrome cérébro-oculo-faciosquelettique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1075. syndrome de Laurence-Moon --- r_associated #0: 26 --> en:roberts syndrome
    n1=syndrome de Laurence-Moon | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1076. syndrome de la selle turcique vide --- r_associated #0: 26 --> en:roberts syndrome
    n1=syndrome de la selle turcique vide | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1077. triskélion --- r_associated #0: 26 --> en:roberts syndrome
    n1=triskélion | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1078. troubles endocriniens, épilepsie et déficience mentale --- r_associated #0: 26 --> en:roberts syndrome
    n1=troubles endocriniens, épilepsie et déficience mentale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=26
  1079. Hyde (prurigo nodulaire de) --- r_associated #0: 25 --> en:roberts syndrome
    n1=Hyde (prurigo nodulaire de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1080. Hölmgren (triade de) --- r_associated #0: 25 --> en:roberts syndrome
    n1=Hölmgren (triade de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1081. S.I.D.A --- r_associated #0: 25 --> en:roberts syndrome
    n1=S.I.D.A | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1082. Syndrome de Li-Fraumeni --- r_associated #0: 25 --> en:roberts syndrome
    n1=Syndrome de Li-Fraumeni | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1083. albinisme avec pigmentation minime --- r_associated #0: 25 --> en:roberts syndrome
    n1=albinisme avec pigmentation minime | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1084. albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception --- r_associated #0: 25 --> en:roberts syndrome
    n1=albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1085. aniridie partielle avec agénésie rénale unilatérale et retard psychomoteur --- r_associated #0: 25 --> en:roberts syndrome
    n1=aniridie partielle avec agénésie rénale unilatérale et retard psychomoteur | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1086. communication interventriculaire --- r_associated #0: 25 --> en:roberts syndrome
    n1=communication interventriculaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1087. crosse aortique(syndrome de la) --- r_associated #0: 25 --> en:roberts syndrome
    n1=crosse aortique(syndrome de la) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1088. dysplasie olfactogénitale --- r_associated #0: 25 --> en:roberts syndrome
    n1=dysplasie olfactogénitale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1089. en:Donohue syndrome --- r_associated #0: 25 --> en:roberts syndrome
    n1=en:Donohue syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1090. en:Dubin-Sprinz disease --- r_associated #0: 25 --> en:roberts syndrome
    n1=en:Dubin-Sprinz disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1091. en:Köbberling's syndrome --- r_associated #0: 25 --> en:roberts syndrome
    n1=en:Köbberling's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1092. en:anasarca --- r_associated #0: 25 --> en:roberts syndrome
    n1=en:anasarca | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1093. en:cysticercal disease --- r_associated #0: 25 --> en:roberts syndrome
    n1=en:cysticercal disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1094. en:dactylolysis spontanea --- r_associated #0: 25 --> en:roberts syndrome
    n1=en:dactylolysis spontanea | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1095. en:deafness --- r_associated #0: 25 --> en:roberts syndrome
    n1=en:deafness | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1096. en:diaphragmatic hernia --- r_associated #0: 25 --> en:roberts syndrome
    n1=en:diaphragmatic hernia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1097. en:erythropoietic uroporphyria --- r_associated #0: 25 --> en:roberts syndrome
    n1=en:erythropoietic uroporphyria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1098. en:hydrops foetalis --- r_associated #0: 25 --> en:roberts syndrome
    n1=en:hydrops foetalis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1099. en:noma --- r_associated #0: 25 --> en:roberts syndrome
    n1=en:noma | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1100. en:oligophrenia --- r_associated #0: 25 --> en:roberts syndrome
    n1=en:oligophrenia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1101. granulomatose éosinophilique avec polyangéite --- r_associated #0: 25 --> en:roberts syndrome
    n1=granulomatose éosinophilique avec polyangéite | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1102. hypogonadisme avec anosmie --- r_associated #0: 25 --> en:roberts syndrome
    n1=hypogonadisme avec anosmie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1103. paragangliome (mise en évidence scintigraphique du) --- r_associated #0: 25 --> en:roberts syndrome
    n1=paragangliome (mise en évidence scintigraphique du) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1104. proptosis --- r_associated #0: 25 --> en:roberts syndrome
    n1=proptosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1105. télécanthus --- r_associated #0: 25 --> en:roberts syndrome
    n1=télécanthus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=25
  1106. Déficience intellectuelle --- r_associated #0: 24 --> en:roberts syndrome
    n1=Déficience intellectuelle | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1107. Goltz (syndrome de) --- r_associated #0: 24 --> en:roberts syndrome
    n1=Goltz (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1108. SRAS --- r_associated #0: 24 --> en:roberts syndrome
    n1=SRAS | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1109. en:Feingold syndrome --- r_associated #0: 24 --> en:roberts syndrome
    n1=en:Feingold syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1110. en:Hurler's syndome --- r_associated #0: 24 --> en:roberts syndrome
    n1=en:Hurler's syndome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1111. en:Laurence-Moon's syndrome --- r_associated #0: 24 --> en:roberts syndrome
    n1=en:Laurence-Moon's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1112. en:Sheehan's syndrome --- r_associated #0: 24 --> en:roberts syndrome
    n1=en:Sheehan's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1113. en:arachnodactily --- r_associated #0: 24 --> en:roberts syndrome
    n1=en:arachnodactily | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1114. en:lazar-house --- r_associated #0: 24 --> en:roberts syndrome
    n1=en:lazar-house | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1115. en:leper colony --- r_associated #0: 24 --> en:roberts syndrome
    n1=en:leper colony | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1116. en:myitis --- r_associated #0: 24 --> en:roberts syndrome
    n1=en:myitis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1117. en:oligopsychia --- r_associated #0: 24 --> en:roberts syndrome
    n1=en:oligopsychia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1118. en:onychoosteodysostosis --- r_associated #0: 24 --> en:roberts syndrome
    n1=en:onychoosteodysostosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1119. en:strabismus syndrome --- r_associated #0: 24 --> en:roberts syndrome
    n1=en:strabismus syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1120. en:type a 14 --- r_associated #0: 24 --> en:roberts syndrome
    n1=en:type a 14 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1121. en:zinc-deficiency type --- r_associated #0: 24 --> en:roberts syndrome
    n1=en:zinc-deficiency type | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1122. insuffisance respiratoire, problème respiratoire --- r_associated #0: 24 --> en:roberts syndrome
    n1=insuffisance respiratoire, problème respiratoire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1123. maladie de roger --- r_associated #0: 24 --> en:roberts syndrome
    n1=maladie de roger | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1124. syndrome cardio-facio-cutané --- r_associated #0: 24 --> en:roberts syndrome
    n1=syndrome cardio-facio-cutané | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1125. syndrome de Joubert-Boltshauser (syndrome de) --- r_associated #0: 24 --> en:roberts syndrome
    n1=syndrome de Joubert-Boltshauser (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  1126. Seitelberger (dystrophie neuroaxonale de) --- r_associated #0: 23 --> en:roberts syndrome
    n1=Seitelberger (dystrophie neuroaxonale de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=23
  1127. acrodermatitis enteropathica --- r_associated #0: 23 --> en:roberts syndrome
    n1=acrodermatitis enteropathica | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=23
  1128. colobome de l'iris avec ptosis, hypertélorisme et retard mental --- r_associated #0: 23 --> en:roberts syndrome
    n1=colobome de l'iris avec ptosis, hypertélorisme et retard mental | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=23
  1129. en:Dubin-Johnson's syndrome --- r_associated #0: 23 --> en:roberts syndrome
    n1=en:Dubin-Johnson's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=23
  1130. en:absent corpus callosum --- r_associated #0: 23 --> en:roberts syndrome
    n1=en:absent corpus callosum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=23
  1131. en:dwarfism --- r_associated #0: 23 --> en:roberts syndrome
    n1=en:dwarfism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=23
  1132. en:leprosarium --- r_associated #0: 23 --> en:roberts syndrome
    n1=en:leprosarium | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=23
  1133. en:polyhydramnion --- r_associated #0: 23 --> en:roberts syndrome
    n1=en:polyhydramnion | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=23
  1134. en:sudden infant death --- r_associated #0: 23 --> en:roberts syndrome
    n1=en:sudden infant death | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=23
  1135. selle turcique vide --- r_associated #0: 23 --> en:roberts syndrome
    n1=selle turcique vide | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=23
  1136. souffrance respiratoire --- r_associated #0: 23 --> en:roberts syndrome
    n1=souffrance respiratoire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=23
  1137. syndrome d'alagille --- r_associated #0: 23 --> en:roberts syndrome
    n1=syndrome d'alagille | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=23
  1138. syndrome de réaction inflammatoire généralisée --- r_associated #0: 23 --> en:roberts syndrome
    n1=syndrome de réaction inflammatoire généralisée | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=23
  1139. FMD --- r_associated #0: 22 --> en:roberts syndrome
    n1=FMD | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=22
  1140. Maladie de Whipple --- r_associated #0: 22 --> en:roberts syndrome
    n1=Maladie de Whipple | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=22
  1141. aniridie, microcornée et cataracte régressive --- r_associated #0: 22 --> en:roberts syndrome
    n1=aniridie, microcornée et cataracte régressive | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=22
  1142. aplasie de la paroi abdominale --- r_associated #0: 22 --> en:roberts syndrome
    n1=aplasie de la paroi abdominale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=22
  1143. brides amniotiques (syndrome des) --- r_associated #0: 22 --> en:roberts syndrome
    n1=brides amniotiques (syndrome des) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=22
  1144. cataracte-atrophie du cervelet-myopathie --- r_associated #0: 22 --> en:roberts syndrome
    n1=cataracte-atrophie du cervelet-myopathie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=22
  1145. chondrodysplasie léthale avec brièveté des côtes --- r_associated #0: 22 --> en:roberts syndrome
    n1=chondrodysplasie léthale avec brièveté des côtes | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=22
  1146. en:Angelman's syndrome --- r_associated #0: 22 --> en:roberts syndrome
    n1=en:Angelman's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=22
  1147. en:X-linked --- r_associated #0: 22 --> en:roberts syndrome
    n1=en:X-linked | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=22
  1148. en:and microgenitalism --- r_associated #0: 22 --> en:roberts syndrome
    n1=en:and microgenitalism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=22
  1149. en:congenital porphyria --- r_associated #0: 22 --> en:roberts syndrome
    n1=en:congenital porphyria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=22
  1150. en:hypopituitarism --- r_associated #0: 22 --> en:roberts syndrome
    n1=en:hypopituitarism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=22
  1151. en:toxemia --- r_associated #0: 22 --> en:roberts syndrome
    n1=en:toxemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=22
  1152. syndrome de sevrage --- r_associated #0: 22 --> en:roberts syndrome
    n1=syndrome de sevrage | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=22
  1153. acatalasémie --- r_associated #0: 21 --> en:roberts syndrome
    n1=acatalasémie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1154. acidurie argininosuccinique --- r_associated #0: 21 --> en:roberts syndrome
    n1=acidurie argininosuccinique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1155. adipose douloureuse de Dercum --- r_associated #0: 21 --> en:roberts syndrome
    n1=adipose douloureuse de Dercum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1156. alcaptonurie --- r_associated #0: 21 --> en:roberts syndrome
    n1=alcaptonurie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1157. anasarque f?toplacentaire --- r_associated #0: 21 --> en:roberts syndrome
    n1=anasarque f?toplacentaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1158. aniridie --- r_associated #0: 21 --> en:roberts syndrome
    n1=aniridie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1159. argininémie --- r_associated #0: 21 --> en:roberts syndrome
    n1=argininémie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1160. calciphylaxie --- r_associated #0: 21 --> en:roberts syndrome
    n1=calciphylaxie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1161. choroïdérémie --- r_associated #0: 21 --> en:roberts syndrome
    n1=choroïdérémie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1162. coproporphyrie héréditaire --- r_associated #0: 21 --> en:roberts syndrome
    n1=coproporphyrie héréditaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1163. en:Caffey's disease --- r_associated #0: 21 --> en:roberts syndrome
    n1=en:Caffey's disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1164. en:Hurler's disease --- r_associated #0: 21 --> en:roberts syndrome
    n1=en:Hurler's disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1165. en:Martin-Bell's syndrome --- r_associated #0: 21 --> en:roberts syndrome
    n1=en:Martin-Bell's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1166. en:Stein-Leventhal syndrome --- r_associated #0: 21 --> en:roberts syndrome
    n1=en:Stein-Leventhal syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1167. en:Stevens-Johnson syndrome --- r_associated #0: 21 --> en:roberts syndrome
    n1=en:Stevens-Johnson syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1168. en:Wegener granulomatosis --- r_associated #0: 21 --> en:roberts syndrome
    n1=en:Wegener granulomatosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1169. en:acute respiratory distress --- r_associated #0: 21 --> en:roberts syndrome
    n1=en:acute respiratory distress | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1170. en:chondrodystrophia punctata --- r_associated #0: 21 --> en:roberts syndrome
    n1=en:chondrodystrophia punctata | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1171. en:marfan's syndrome --- r_associated #0: 21 --> en:roberts syndrome
    n1=en:marfan's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1172. en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) --- r_associated #0: 21 --> en:roberts syndrome
    n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1173. en:sarcitis --- r_associated #0: 21 --> en:roberts syndrome
    n1=en:sarcitis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1174. hypopituitarisme --- r_associated #0: 21 --> en:roberts syndrome
    n1=hypopituitarisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1175. idiosyncrasie au fructose --- r_associated #0: 21 --> en:roberts syndrome
    n1=idiosyncrasie au fructose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1176. proptose oculaire --- r_associated #0: 21 --> en:roberts syndrome
    n1=proptose oculaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1177. sclérotique bleue --- r_associated #0: 21 --> en:roberts syndrome
    n1=sclérotique bleue | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1178. syndrome de Churg-Strauss --- r_associated #0: 21 --> en:roberts syndrome
    n1=syndrome de Churg-Strauss | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1179. syndrome de Prader-Willi --- r_associated #0: 21 --> en:roberts syndrome
    n1=syndrome de Prader-Willi | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1180. syndrome des ongles jaunes --- r_associated #0: 21 --> en:roberts syndrome
    n1=syndrome des ongles jaunes | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1181. xanthique (lithiase) --- r_associated #0: 21 --> en:roberts syndrome
    n1=xanthique (lithiase) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1182. xérophtalmie --- r_associated #0: 21 --> en:roberts syndrome
    n1=xérophtalmie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21
  1183. ARTHROGRYPOSE --- r_associated #0: 20 --> en:roberts syndrome
    n1=ARTHROGRYPOSE | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1184. Hydramnios --- r_associated #0: 20 --> en:roberts syndrome
    n1=Hydramnios | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1185. dysplasie olfactogénitale de De Morsier --- r_associated #0: 20 --> en:roberts syndrome
    n1=dysplasie olfactogénitale de De Morsier | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1186. en:1p36 deletion syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:1p36 deletion syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1187. en:5' 10' methylenetetrahydrofolate reductase deficiency --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:5' 10' methylenetetrahydrofolate reductase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1188. en:aagenaes syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:aagenaes syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1189. en:abetalipoproteinemia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:abetalipoproteinemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1190. en:abnormal nuclear morphology --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:abnormal nuclear morphology | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1191. en:absence or reduction in length of femur, tibia, or fibula --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:absence or reduction in length of femur, tibia, or fibula | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1192. en:absence or reduction in length of humerus, radius, or ulna --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:absence or reduction in length of humerus, radius, or ulna | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1193. en:absent earlobe --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:absent earlobe | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1194. en:accessory spleen --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:accessory spleen | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1195. en:achenbach syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:achenbach syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1196. en:achromatopsia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:achromatopsia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1197. en:acrocephalosyndactyly --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:acrocephalosyndactyly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1198. en:acroparesthesia syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:acroparesthesia syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1199. en:acute coronary syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:acute coronary syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1200. en:acute intermittent porphyria --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:acute intermittent porphyria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1201. en:adherence syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:adherence syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1202. en:alper syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:alper syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1203. en:alstrom syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:alstrom syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1204. en:amaurosis fugax --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:amaurosis fugax | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1205. en:analbuminemia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:analbuminemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1206. en:andersen syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:andersen syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1207. en:ankle contracture --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:ankle contracture | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1208. en:antiphospholipid syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:antiphospholipid syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1209. en:antithrombin iii deficiency --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:antithrombin iii deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1210. en:aprosencephaly --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:aprosencephaly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1211. en:barrett esophagus --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:barrett esophagus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1212. en:bartter syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:bartter syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1213. en:basilar artery syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:basilar artery syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1214. en:birth weight 1.5-2.2 kg --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:birth weight 1.5-2.2 kg | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1215. en:bloom syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:bloom syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1216. en:brown-sequard syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:brown-sequard syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1217. en:camurati-engelmann syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:camurati-engelmann syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1218. en:capgras syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:capgras syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1219. en:capillary leak syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:capillary leak syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1220. en:cardiorenal syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:cardiorenal syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1221. en:carnitine palmitoyltransferase ii deficiency --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:carnitine palmitoyltransferase ii deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1222. en:carnosinemia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:carnosinemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1223. en:carpal tunnel syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:carpal tunnel syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1224. en:cartilage hair hypoplasia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:cartilage hair hypoplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1225. en:cataract --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:cataract | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1226. en:central sleep apnea syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:central sleep apnea syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1227. en:cerebellar mutism --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:cerebellar mutism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1228. en:cervicocranial syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:cervicocranial syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1229. en:chediak-higashi syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:chediak-higashi syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1230. en:chorea --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:chorea | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1231. en:chronic fatigue syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:chronic fatigue syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1232. en:cleft lip --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:cleft lip | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1233. en:cleft palate --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:cleft palate | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1234. en:coffin-siris syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:coffin-siris syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1235. en:coloboma of the eyelid --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:coloboma of the eyelid | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1236. en:complete trisomy 21 syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:complete trisomy 21 syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1237. en:congenital central hypoventilation --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:congenital central hypoventilation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1238. en:congenital clinodactyly --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:congenital clinodactyly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1239. en:congenital insensitivity to pain with anhidrosis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:congenital insensitivity to pain with anhidrosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1240. en:congenital myasthenic syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:congenital myasthenic syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1241. en:contracture of elbow --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:contracture of elbow | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1242. en:contracture of knee --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:contracture of knee | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1243. en:contracture of wrist joint --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:contracture of wrist joint | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1244. en:corneal haze --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:corneal haze | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1245. en:crest syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:crest syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1246. en:cryopyrin-associated periodic syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:cryopyrin-associated periodic syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1247. en:cutis laxa --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:cutis laxa | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1248. en:cystathioninuria --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:cystathioninuria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1249. en:cystinuria --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:cystinuria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1250. en:cytokine release syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:cytokine release syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1251. en:d-bifunctional protein deficiency --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:d-bifunctional protein deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1252. en:dandy-walker malformation --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:dandy-walker malformation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1253. en:de sanctis-cacchione syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:de sanctis-cacchione syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1254. en:dialyzer first use syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:dialyzer first use syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1255. en:diarrhea-associated hemolytic uremic syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:diarrhea-associated hemolytic uremic syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1256. en:diencephalic syndrome of infancy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:diencephalic syndrome of infancy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1257. en:diethylstilbestrol syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:diethylstilbestrol syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1258. en:diffuse cerebral sclerosis of schilder --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:diffuse cerebral sclerosis of schilder | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1259. en:diffuse idiopathic skeletal hyperostosis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:diffuse idiopathic skeletal hyperostosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1260. en:diffuse infiltrative lymphocytosis syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:diffuse infiltrative lymphocytosis syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1261. en:downward slant of palpebral fissure --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:downward slant of palpebral fissure | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1262. en:dubowitz syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:dubowitz syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1263. en:dyggve-melchior-clausen syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:dyggve-melchior-clausen syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1264. en:ectromelia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:ectromelia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1265. en:ehlers-danlos syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:ehlers-danlos syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1266. en:eisenmenger syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:eisenmenger syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1267. en:encephalocele --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:encephalocele | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1268. en:encephaloceles, frontal --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:encephaloceles, frontal | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1269. en:epidermolysis bullosa --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:epidermolysis bullosa | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1270. en:erythrokeratodermia variabilis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:erythrokeratodermia variabilis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1271. en:evans syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:evans syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1272. en:exfoliation syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:exfoliation syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1273. en:familial juvenile nephronophthisis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:familial juvenile nephronophthisis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1274. en:familial mediterranean fever --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:familial mediterranean fever | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1275. en:fanconi syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:fanconi syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1276. en:felty syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:felty syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1277. en:fetal akinesia deformation sequence --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:fetal akinesia deformation sequence | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1278. en:fetal alcohol syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:fetal alcohol syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1279. en:fetal methotrexate syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:fetal methotrexate syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1280. en:fetal valproate syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:fetal valproate syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1281. en:fetal warfarin syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:fetal warfarin syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1282. en:fibromuscular dysplasia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:fibromuscular dysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1283. en:fraser syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:fraser syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1284. en:frasier syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:frasier syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1285. en:freeman-sheldon syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:freeman-sheldon syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1286. en:friedreich ataxia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:friedreich ataxia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1287. en:fryns syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:fryns syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1288. en:fuchs endothelial dystrophy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:fuchs endothelial dystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1289. en:gasping syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:gasping syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1290. en:gastric antral vascular ectasia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:gastric antral vascular ectasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1291. en:gastroschisis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:gastroschisis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1292. en:genu varum --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:genu varum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1293. en:giant axonal neuropathy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:giant axonal neuropathy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1294. en:gilbert syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:gilbert syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1295. en:glycine encephalopathy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:glycine encephalopathy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1296. en:goodpasture syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:goodpasture syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1297. en:gynatresia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:gynatresia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1298. en:gyrate atrophy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:gyrate atrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1299. en:hajdu-cheney syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hajdu-cheney syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1300. en:hellp syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hellp syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1301. en:hemochromatosis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hemochromatosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1302. en:hemophagocytic lymphohistiocytosis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hemophagocytic lymphohistiocytosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1303. en:hemophagocytic syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hemophagocytic syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1304. en:hemorrhagic fever with renal syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hemorrhagic fever with renal syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1305. en:hepatolenticular degeneration --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hepatolenticular degeneration | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1306. en:hepatorenal syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hepatorenal syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1307. en:hereditary benign intraepithelial dyskeratosis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hereditary benign intraepithelial dyskeratosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1308. en:heterotaxy syndrome with polysplenia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:heterotaxy syndrome with polysplenia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1309. en:homocystinuria --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:homocystinuria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1310. en:horseshoe kidney --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:horseshoe kidney | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1311. en:hurler-scheie syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hurler-scheie syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1312. en:hypereosinophilic syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hypereosinophilic syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1313. en:hyperglycerolemia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hyperglycerolemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1314. en:hyperkalemic periodic paralysis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hyperkalemic periodic paralysis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1315. en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1316. en:hypoalphalipoproteinemia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hypoalphalipoproteinemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1317. en:hypokalemic periodic paralysis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hypokalemic periodic paralysis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1318. en:hypomelia (more severe in upper limbs) --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hypomelia (more severe in upper limbs) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1319. en:hypophosphatasia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hypophosphatasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1320. en:hypoplastic left heart syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hypoplastic left heart syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1321. en:hypoplastic right heart syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:hypoplastic right heart syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1322. en:idiopathic cd4-positive t-lymphocytopenia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:idiopathic cd4-positive t-lymphocytopenia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1323. en:immune reconstitution inflammatory syndrome associated with kaposi sarcoma --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:immune reconstitution inflammatory syndrome associated with kaposi sarcoma | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1324. en:immunodeficiency syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:immunodeficiency syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1325. en:immunoglobulin a deficiency 1 --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:immunoglobulin a deficiency 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1326. en:imperforate vagina --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:imperforate vagina | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1327. en:incontinentia pigmenti --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:incontinentia pigmenti | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1328. en:increased size of penis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:increased size of penis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1329. en:intestinal atresia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:intestinal atresia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1330. en:iridocorneal endothelial syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:iridocorneal endothelial syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1331. en:irritable bowel syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:irritable bowel syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1332. en:jeune syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:jeune syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1333. en:joubert syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:joubert syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1334. en:kartagener syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:kartagener syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1335. en:klippel-feil syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:klippel-feil syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1336. en:klippel-trenaunay-weber syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:klippel-trenaunay-weber syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1337. en:kluver-bucy syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:kluver-bucy syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1338. en:kniest dysplasia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:kniest dysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1339. en:lafora disease --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:lafora disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1340. en:landau-kleffner syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:landau-kleffner syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1341. en:lateral medullary syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:lateral medullary syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1342. en:leber congenital amaurosis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:leber congenital amaurosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1343. en:leber hereditary optic atrophy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:leber hereditary optic atrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1344. en:lecithin acyltransferase deficiency --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:lecithin acyltransferase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1345. en:left ventricular non-compaction syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:left ventricular non-compaction syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1346. en:lennox-gastaut syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:lennox-gastaut syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1347. en:leptospirosis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:leptospirosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1348. en:leukodystrophy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:leukodystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1349. en:lipoid proteinosis of urbach and wiethe --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:lipoid proteinosis of urbach and wiethe | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1350. en:loeys-dietz syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:loeys-dietz syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1351. en:loffler syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:loffler syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1352. en:long qt syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:long qt syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1353. en:low set ears --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:low set ears | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1354. en:lymphedema-distichiasis syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:lymphedema-distichiasis syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1355. en:lysinuric protein intolerance --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:lysinuric protein intolerance | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1356. en:machado-joseph disease --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:machado-joseph disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1357. en:malakoplakia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:malakoplakia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1358. en:malformations of cortical development --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:malformations of cortical development | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1359. en:mandibuloacral dysplasia with type a lipodystrophy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:mandibuloacral dysplasia with type a lipodystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1360. en:mansonelliasis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:mansonelliasis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1361. en:mayer-rokitansky-kuster-hauser syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:mayer-rokitansky-kuster-hauser syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1362. en:medium-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:medium-chain acyl-coa dehydrogenase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1363. en:melkersson-rosenthal syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:melkersson-rosenthal syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1364. en:melorheostosis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:melorheostosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1365. en:menopausal syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:menopausal syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1366. en:merrf syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:merrf syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1367. en:methylmalonic acidemia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:methylmalonic acidemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1368. en:mevalonate kinase deficiency --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:mevalonate kinase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1369. en:microcephaly --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:microcephaly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1370. en:midface capillary hemangioma --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:midface capillary hemangioma | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1371. en:migrating partial seizures in infancy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:migrating partial seizures in infancy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1372. en:miliaria --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:miliaria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1373. en:mixed connective tissue disease --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:mixed connective tissue disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1374. en:mmih syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:mmih syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1375. en:molybdenum cofactor deficiency --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:molybdenum cofactor deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1376. en:monilethrix --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:monilethrix | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1377. en:moyamoya disease --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:moyamoya disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1378. en:muenke syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:muenke syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1379. en:mulibrey nanism --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:mulibrey nanism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1380. en:multiple system atrophy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:multiple system atrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1381. en:muscular dystrophy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:muscular dystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1382. en:nadh dehydrogenase deficiency --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:nadh dehydrogenase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1383. en:nephrogenic fibrosing dermopathy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:nephrogenic fibrosing dermopathy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1384. en:nephrotic syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:nephrotic syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1385. en:neuroleptic malignant syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:neuroleptic malignant syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1386. en:neuromyelitis optica --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:neuromyelitis optica | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1387. en:ochronosis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:ochronosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1388. en:oculocerebrorenal syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:oculocerebrorenal syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1389. en:oligodactyly --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:oligodactyly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1390. en:olivopontocerebellar atrophy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:olivopontocerebellar atrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1391. en:organic brain syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:organic brain syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1392. en:orofaciodigital syndrome type 1 --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:orofaciodigital syndrome type 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1393. en:otopalatodigital syndrome type 1 --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:otopalatodigital syndrome type 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1394. en:overlap syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:overlap syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1395. en:pain amplification syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:pain amplification syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1396. en:pallister-hall syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:pallister-hall syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1397. en:pallister-killian syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:pallister-killian syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1398. en:pancreatic lipase deficiency --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:pancreatic lipase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1399. en:pantothenate kinase-associated neurodegeneration --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:pantothenate kinase-associated neurodegeneration | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1400. en:paraneoplastic syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:paraneoplastic syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1401. en:parinaud syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:parinaud syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1402. en:patent ductus arteriosus --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:patent ductus arteriosus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1403. en:pelger-huet anomaly --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:pelger-huet anomaly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1404. en:pemphigoid gestationis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:pemphigoid gestationis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1405. en:perinatal blood aspiration syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:perinatal blood aspiration syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1406. en:perlman syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:perlman syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1407. en:peters-plus syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:peters-plus syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1408. en:phosphoenolpyruvate carboxykinase deficiency --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:phosphoenolpyruvate carboxykinase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1409. en:pinta --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:pinta | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1410. en:piriformis muscle syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:piriformis muscle syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1411. en:pituitary stalk interruption syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:pituitary stalk interruption syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1412. en:pityriasis lichenoides --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:pityriasis lichenoides | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1413. en:poems syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:poems syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1414. en:polymyalgia rheumatica --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:polymyalgia rheumatica | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1415. en:popliteal pterygium syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:popliteal pterygium syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1416. en:porokeratosis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:porokeratosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1417. en:post-pericardiotomy syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:post-pericardiotomy syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1418. en:posterior fossa syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:posterior fossa syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1419. en:posteriorly rotated ear --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:posteriorly rotated ear | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1420. en:postural orthostatic tachycardia syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:postural orthostatic tachycardia syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1421. en:potocki-lupski syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:potocki-lupski syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1422. en:pre-excitation syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:pre-excitation syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1423. en:prekallikrein deficiency --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:prekallikrein deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1424. en:premenstrual syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:premenstrual syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1425. en:primary fanconi syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:primary fanconi syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1426. en:primary hypertrophic osteoarthropathy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:primary hypertrophic osteoarthropathy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1427. en:progressive hemifacial atrophy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:progressive hemifacial atrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1428. en:progressive muscular atrophy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:progressive muscular atrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1429. en:prosopagnosia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:prosopagnosia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1430. en:proteus syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:proteus syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1431. en:pseudohermaphroditism --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:pseudohermaphroditism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1432. en:pseudohypoaldosteronism --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:pseudohypoaldosteronism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1433. en:pseudoxanthoma elasticum --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:pseudoxanthoma elasticum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1434. en:radial aplasia-thrombocytopenia syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:radial aplasia-thrombocytopenia syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1435. en:radiation sickness syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:radiation sickness syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1436. en:reiter syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:reiter syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1437. en:renal cysts and diabetes syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:renal cysts and diabetes syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1438. en:retinoschisis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:retinoschisis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1439. en:reye syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:reye syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1440. en:roberts-sc phocomelia syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:roberts-sc phocomelia syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1441. en:scimitar syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:scimitar syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1442. en:scleredema adultorum --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:scleredema adultorum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1443. en:sea-blue histiocyte syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:sea-blue histiocyte syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1444. en:seckel syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:seckel syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1445. en:shone syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:shone syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1446. en:short neck --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:short neck | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1447. en:sick sinus syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:sick sinus syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1448. en:sitosterolemia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:sitosterolemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1449. en:sjogren syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:sjogren syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1450. en:smith-lemli-opitz syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:smith-lemli-opitz syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1451. en:spasmodic torticollis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:spasmodic torticollis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1452. en:spinal muscular atrophy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:spinal muscular atrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1453. en:spondyloepimetaphyseal dysplasia, sponastrime type --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:spondyloepimetaphyseal dysplasia, sponastrime type | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1454. en:staphylococcal scalded skin syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:staphylococcal scalded skin syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1455. en:status epilepticus --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:status epilepticus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1456. en:stickler syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:stickler syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1457. en:stiff person syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:stiff person syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1458. en:stiff skin syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:stiff skin syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1459. en:subclavian steal syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:subclavian steal syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1460. en:sunct syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:sunct syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1461. en:superior vena cava syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:superior vena cava syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1462. en:susac syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:susac syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1463. en:sweet syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:sweet syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1464. en:swyer james syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:swyer james syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1465. en:syndactyly --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:syndactyly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1466. en:synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1467. en:syringomyelia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:syringomyelia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1468. en:talipes equinovalgus --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:talipes equinovalgus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1469. en:tangier disease --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:tangier disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1470. en:teething syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:teething syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1471. en:tethered spinal cord syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:tethered spinal cord syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1472. en:tetraphocomelia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:tetraphocomelia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1473. en:thalidomide embryopathy syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:thalidomide embryopathy syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1474. en:thanatophoric dysplasia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:thanatophoric dysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1475. en:thoracic outlet syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:thoracic outlet syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1476. en:tooth and nail syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:tooth and nail syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1477. en:tourette syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:tourette syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1478. en:tracheobronchomalacia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:tracheobronchomalacia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1479. en:transient global amnesia --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:transient global amnesia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1480. en:trichinosis --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:trichinosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1481. en:trichorhinophalangeal syndrome type i --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:trichorhinophalangeal syndrome type i | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1482. en:true hermaphroditism --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:true hermaphroditism | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1483. en:turner syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:turner syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1484. en:undescended testes --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:undescended testes | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1485. en:uniparental disomy --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:uniparental disomy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1486. en:usher syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:usher syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1487. en:uveitis glaucoma and hyphema syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:uveitis glaucoma and hyphema syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1488. en:van der woude syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:van der woude syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1489. en:vascular access steal syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:vascular access steal syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1490. en:very long-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:very long-chain acyl-coa dehydrogenase deficiency | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1491. en:wandering spleen --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:wandering spleen | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1492. en:weaver syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:weaver syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1493. en:weill-marchesani syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:weill-marchesani syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1494. en:werner syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:werner syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1495. en:wolff-parkinson-white syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:wolff-parkinson-white syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1496. en:xxxy syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:xxxy syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1497. en:xxyy syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:xxyy syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1498. en:xyy syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:xyy syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1499. en:zollinger ellison syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=en:zollinger ellison syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1500. leptospirose --- r_associated #0: 20 --> en:roberts syndrome
    n1=leptospirose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1501. syndrome --- r_associated #0: 20 --> en:roberts syndrome
    n1=syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
  1502. triploïdie --- r_associated #0: 16 --> en:roberts syndrome
    n1=triploïdie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=16
  1503. trisomie 21 --- r_associated #0: 16 --> en:roberts syndrome
    n1=trisomie 21 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=16
  1504. Albert (position d') --- r_associated #0: 15 --> en:roberts syndrome
    n1=Albert (position d') | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1505. Anomalie d'Ebstein --- r_associated #0: 15 --> en:roberts syndrome
    n1=Anomalie d'Ebstein | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1506. Arrhenius (loi d') --- r_associated #0: 15 --> en:roberts syndrome
    n1=Arrhenius (loi d') | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1507. Arthrogrypose --- r_associated #0: 15 --> en:roberts syndrome
    n1=Arthrogrypose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1508. Bracht (manoeuvre de) --- r_associated #0: 15 --> en:roberts syndrome
    n1=Bracht (manoeuvre de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1509. Détresse respiratoire --- r_associated #0: 15 --> en:roberts syndrome
    n1=Détresse respiratoire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1510. Giessen (test de) --- r_associated #0: 15 --> en:roberts syndrome
    n1=Giessen (test de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1511. Intolérance au fructose --- r_associated #0: 15 --> en:roberts syndrome
    n1=Intolérance au fructose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1512. Kallman --- r_associated #0: 15 --> en:roberts syndrome
    n1=Kallman | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1513. Maladie de Marfan --- r_associated #0: 15 --> en:roberts syndrome
    n1=Maladie de Marfan | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1514. Noma --- r_associated #0: 15 --> en:roberts syndrome
    n1=Noma | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1515. Syndrome d'immunodéficience acquise --- r_associated #0: 15 --> en:roberts syndrome
    n1=Syndrome d'immunodéficience acquise | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1516. Syndrome de Walker-Warburg --- r_associated #0: 15 --> en:roberts syndrome
    n1=Syndrome de Walker-Warburg | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1517. Syndrome de sevrage --- r_associated #0: 15 --> en:roberts syndrome
    n1=Syndrome de sevrage | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1518. acidoses lactiques (classification selon Cohen et Woods) --- r_associated #0: 15 --> en:roberts syndrome
    n1=acidoses lactiques (classification selon Cohen et Woods) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1519. agglutinines froides (neuropathie à) --- r_associated #0: 15 --> en:roberts syndrome
    n1=agglutinines froides (neuropathie à) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1520. cysticercoïde (larve) --- r_associated #0: 15 --> en:roberts syndrome
    n1=cysticercoïde (larve) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1521. dysembryome (bénin, malin) --- r_associated #0: 15 --> en:roberts syndrome
    n1=dysembryome (bénin, malin) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1522. dégénérescence wallerienne --- r_associated #0: 15 --> en:roberts syndrome
    n1=dégénérescence wallerienne | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1523. démence (sémiologie) --- r_associated #0: 15 --> en:roberts syndrome
    n1=démence (sémiologie) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1524. en:hydramnion --- r_associated #0: 15 --> en:roberts syndrome
    n1=en:hydramnion | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1525. goltz --- r_associated #0: 15 --> en:roberts syndrome
    n1=goltz | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1526. handicap mental --- r_associated #0: 15 --> en:roberts syndrome
    n1=handicap mental | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1527. hydrocèle (cure chirurgicale d') --- r_associated #0: 15 --> en:roberts syndrome
    n1=hydrocèle (cure chirurgicale d') | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1528. hypophosphatasie --- r_associated #0: 15 --> en:roberts syndrome
    n1=hypophosphatasie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1529. iceberg (signe de l') --- r_associated #0: 15 --> en:roberts syndrome
    n1=iceberg (signe de l') | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1530. maladie à virus de marburg --- r_associated #0: 15 --> en:roberts syndrome
    n1=maladie à virus de marburg | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1531. osteopœcilie --- r_associated #0: 15 --> en:roberts syndrome
    n1=osteopœcilie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1532. snm --- r_associated #0: 15 --> en:roberts syndrome
    n1=snm | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1533. syndrome de Kallman-de Morsier --- r_associated #0: 15 --> en:roberts syndrome
    n1=syndrome de Kallman-de Morsier | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1534. syndrome de Korsakoff --- r_associated #0: 15 --> en:roberts syndrome
    n1=syndrome de Korsakoff | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1535. syndrome de Plummer-VInson --- r_associated #0: 15 --> en:roberts syndrome
    n1=syndrome de Plummer-VInson | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1536. syndrome de de Morsier-Kallmann --- r_associated #0: 15 --> en:roberts syndrome
    n1=syndrome de de Morsier-Kallmann | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1537. syndrome malin neuroleptique --- r_associated #0: 15 --> en:roberts syndrome
    n1=syndrome malin neuroleptique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1538. triple arthrodèse --- r_associated #0: 15 --> en:roberts syndrome
    n1=triple arthrodèse | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1539. triple opération à la française --- r_associated #0: 15 --> en:roberts syndrome
    n1=triple opération à la française | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1540. triptans --- r_associated #0: 15 --> en:roberts syndrome
    n1=triptans | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1541. triquétrum --- r_associated #0: 15 --> en:roberts syndrome
    n1=triquétrum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1542. triradialis sulcus de Turner --- r_associated #0: 15 --> en:roberts syndrome
    n1=triradialis sulcus de Turner | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1543. tris --- r_associated #0: 15 --> en:roberts syndrome
    n1=tris | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1544. trismus --- r_associated #0: 15 --> en:roberts syndrome
    n1=trismus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1545. trisomie du bras court du chromosome 3 --- r_associated #0: 15 --> en:roberts syndrome
    n1=trisomie du bras court du chromosome 3 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1546. xérophthalmie --- r_associated #0: 15 --> en:roberts syndrome
    n1=xérophthalmie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=15
  1547. aprosencéphalie --- r_associated #0: 11 --> en:roberts syndrome
    n1=aprosencéphalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=11
  1548. dysautonomie familiale --- r_associated #0: 11 --> en:roberts syndrome
    n1=dysautonomie familiale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=11
  1549. hydranencéphalie --- r_associated #0: 11 --> en:roberts syndrome
    n1=hydranencéphalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=11
  1550. hydrencéphalie --- r_associated #0: 11 --> en:roberts syndrome
    n1=hydrencéphalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=11
  1551. insomnie familiale fatale --- r_associated #0: 11 --> en:roberts syndrome
    n1=insomnie familiale fatale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=11
  1552. lepréchaunisme --- r_associated #0: 11 --> en:roberts syndrome
    n1=lepréchaunisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=11
  1553. maladie de Fox-Fordyce --- r_associated #0: 11 --> en:roberts syndrome
    n1=maladie de Fox-Fordyce | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=11
  1554. mongolisme --- r_associated #0: 11 --> en:roberts syndrome
    n1=mongolisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=11
  1555. rétinoschisis --- r_associated #0: 11 --> en:roberts syndrome
    n1=rétinoschisis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=11
  1556. syndrome de Gitelman --- r_associated #0: 11 --> en:roberts syndrome
    n1=syndrome de Gitelman | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=11
  1557. syndrome de Warburg --- r_associated #0: 11 --> en:roberts syndrome
    n1=syndrome de Warburg | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=11
  1558. Acromégalie --- r_associated #0: 10 --> en:roberts syndrome
    n1=Acromégalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1559. Agnosie --- r_associated #0: 10 --> en:roberts syndrome
    n1=Agnosie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1560. Albinisme --- r_associated #0: 10 --> en:roberts syndrome
    n1=Albinisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1561. Alice au pays des merveilles (syndrome d') --- r_associated #0: 10 --> en:roberts syndrome
    n1=Alice au pays des merveilles (syndrome d') | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1562. Anencéphalie --- r_associated #0: 10 --> en:roberts syndrome
    n1=Anencéphalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1563. Angelman (syndrome d') --- r_associated #0: 10 --> en:roberts syndrome
    n1=Angelman (syndrome d') | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1564. Brachydactylie --- r_associated #0: 10 --> en:roberts syndrome
    n1=Brachydactylie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1565. Cataplexie --- r_associated #0: 10 --> en:roberts syndrome
    n1=Cataplexie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1566. Communication interauriculaire --- r_associated #0: 10 --> en:roberts syndrome
    n1=Communication interauriculaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1567. Craniosynostose --- r_associated #0: 10 --> en:roberts syndrome
    n1=Craniosynostose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1568. Cysticercose --- r_associated #0: 10 --> en:roberts syndrome
    n1=Cysticercose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1569. Dercum (maladie de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Dercum (maladie de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1570. Dubin-Johnson (syndrome de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Dubin-Johnson (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1571. Dugbe (virus) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Dugbe (virus) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1572. Déficience mentale --- r_associated #0: 10 --> en:roberts syndrome
    n1=Déficience mentale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1573. Exophtalmie --- r_associated #0: 10 --> en:roberts syndrome
    n1=Exophtalmie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1574. Fibromyalgie --- r_associated #0: 10 --> en:roberts syndrome
    n1=Fibromyalgie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1575. Glycogénose --- r_associated #0: 10 --> en:roberts syndrome
    n1=Glycogénose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1576. HELLP syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=HELLP syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1577. HLP3 --- r_associated #0: 10 --> en:roberts syndrome
    n1=HLP3 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1578. HPE3 --- r_associated #0: 10 --> en:roberts syndrome
    n1=HPE3 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1579. HPE4 --- r_associated #0: 10 --> en:roberts syndrome
    n1=HPE4 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1580. Haltia-Santavuori (maladie de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Haltia-Santavuori (maladie de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1581. Hurler (maladie de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Hurler (maladie de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1582. Hydrocéphalie --- r_associated #0: 10 --> en:roberts syndrome
    n1=Hydrocéphalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1583. Hypertélorisme --- r_associated #0: 10 --> en:roberts syndrome
    n1=Hypertélorisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1584. Hypopituitarisme --- r_associated #0: 10 --> en:roberts syndrome
    n1=Hypopituitarisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1585. Hypoxémie --- r_associated #0: 10 --> en:roberts syndrome
    n1=Hypoxémie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1586. Insler et Bernstein (score cervical d') --- r_associated #0: 10 --> en:roberts syndrome
    n1=Insler et Bernstein (score cervical d') | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1587. Laurence-Moon (syndrome de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Laurence-Moon (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1588. Levine-Critchley (syndrome de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Levine-Critchley (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1589. Lisfranc (fracture de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Lisfranc (fracture de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1590. Léproserie --- r_associated #0: 10 --> en:roberts syndrome
    n1=Léproserie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1591. Maladie de Kawasaki --- r_associated #0: 10 --> en:roberts syndrome
    n1=Maladie de Kawasaki | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1592. Malformation d'Ebstein --- r_associated #0: 10 --> en:roberts syndrome
    n1=Malformation d'Ebstein | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1593. Marburg (fièvre de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Marburg (fièvre de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1594. Martin-Bell (syndrome de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Martin-Bell (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1595. Micrognathie --- r_associated #0: 10 --> en:roberts syndrome
    n1=Micrognathie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1596. Mort subite du nourrisson --- r_associated #0: 10 --> en:roberts syndrome
    n1=Mort subite du nourrisson | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1597. Myosite --- r_associated #0: 10 --> en:roberts syndrome
    n1=Myosite | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1598. PMDS --- r_associated #0: 10 --> en:roberts syndrome
    n1=PMDS | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1599. PMI gene --- r_associated #0: 10 --> en:roberts syndrome
    n1=PMI gene | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1600. Panum (aire de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Panum (aire de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1601. Peste noire --- r_associated #0: 10 --> en:roberts syndrome
    n1=Peste noire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1602. Pitt-Rogers-Danks (syndrome de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Pitt-Rogers-Danks (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1603. Polyhydramnios --- r_associated #0: 10 --> en:roberts syndrome
    n1=Polyhydramnios | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1604. Progéria --- r_associated #0: 10 --> en:roberts syndrome
    n1=Progéria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1605. Roger (maladie de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Roger (maladie de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1606. Sheehan (syndrome de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Sheehan (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1607. Shy-Drager (syndrome de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Shy-Drager (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1608. Sicard (opération de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Sicard (opération de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1609. Situs inversus --- r_associated #0: 10 --> en:roberts syndrome
    n1=Situs inversus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1610. Stargardt (maladie de ) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Stargardt (maladie de ) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1611. Stilling-Türk-Duane (syndrome de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Stilling-Türk-Duane (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1612. Syndrome de Churg-Strauss --- r_associated #0: 10 --> en:roberts syndrome
    n1=Syndrome de Churg-Strauss | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1613. Syndrome de Mayer-Rokitansky-Küster-Hauser --- r_associated #0: 10 --> en:roberts syndrome
    n1=Syndrome de Mayer-Rokitansky-Küster-Hauser | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1614. Syndrome de Prader-Willi --- r_associated #0: 10 --> en:roberts syndrome
    n1=Syndrome de Prader-Willi | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1615. Syndrome de Sheehan --- r_associated #0: 10 --> en:roberts syndrome
    n1=Syndrome de Sheehan | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1616. Syndrome de Sotos --- r_associated #0: 10 --> en:roberts syndrome
    n1=Syndrome de Sotos | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1617. Syndrome de détresse respiratoire --- r_associated #0: 10 --> en:roberts syndrome
    n1=Syndrome de détresse respiratoire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1618. Syndrome de malabsorption --- r_associated #0: 10 --> en:roberts syndrome
    n1=Syndrome de malabsorption | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1619. Syndrome du choc toxique --- r_associated #0: 10 --> en:roberts syndrome
    n1=Syndrome du choc toxique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1620. Syndrome métabolique --- r_associated #0: 10 --> en:roberts syndrome
    n1=Syndrome métabolique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1621. Townes-Brocks (syndrome de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Townes-Brocks (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1622. Trichothiodystrophie --- r_associated #0: 10 --> en:roberts syndrome
    n1=Trichothiodystrophie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1623. Trisomie --- r_associated #0: 10 --> en:roberts syndrome
    n1=Trisomie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1624. Völker-Dieben (atrophie optique liée au sexe de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Völker-Dieben (atrophie optique liée au sexe de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1625. Wegener (granulomatose de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Wegener (granulomatose de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1626. Went (atrophie optique liée au sexe de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Went (atrophie optique liée au sexe de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1627. Yellen-Gomco (clamp de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=Yellen-Gomco (clamp de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1628. a-bêta-lipoprotéinémie --- r_associated #0: 10 --> en:roberts syndrome
    n1=a-bêta-lipoprotéinémie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1629. achondrogénèses --- r_associated #0: 10 --> en:roberts syndrome
    n1=achondrogénèses | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1630. achromatopsie --- r_associated #0: 10 --> en:roberts syndrome
    n1=achromatopsie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1631. alcalose métabolique (classification) --- r_associated #0: 10 --> en:roberts syndrome
    n1=alcalose métabolique (classification) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1632. allocations --- r_associated #0: 10 --> en:roberts syndrome
    n1=allocations | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1633. angl. TBS --- r_associated #0: 10 --> en:roberts syndrome
    n1=angl. TBS | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1634. angl. XLSA/A --- r_associated #0: 10 --> en:roberts syndrome
    n1=angl. XLSA/A | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1635. aniline (intoxication par l') --- r_associated #0: 10 --> en:roberts syndrome
    n1=aniline (intoxication par l') | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1636. association de tics vocaux et tics moteurs du syndrome de gilles de la tourette --- r_associated #0: 10 --> en:roberts syndrome
    n1=association de tics vocaux et tics moteurs du syndrome de gilles de la tourette | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1637. chondrodysplasie ponctuée --- r_associated #0: 10 --> en:roberts syndrome
    n1=chondrodysplasie ponctuée | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1638. coproantigènes (recherche de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=coproantigènes (recherche de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1639. cutis laxa --- r_associated #0: 10 --> en:roberts syndrome
    n1=cutis laxa | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1640. diabète bronzé --- r_associated #0: 10 --> en:roberts syndrome
    n1=diabète bronzé | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1641. distance interpédiculaire (mesure de la) --- r_associated #0: 10 --> en:roberts syndrome
    n1=distance interpédiculaire (mesure de la) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1642. dysplasie frontométaphysaire --- r_associated #0: 10 --> en:roberts syndrome
    n1=dysplasie frontométaphysaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1643. dysplasie génitale --- r_associated #0: 10 --> en:roberts syndrome
    n1=dysplasie génitale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1644. dysplasie iridodentaire --- r_associated #0: 10 --> en:roberts syndrome
    n1=dysplasie iridodentaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1645. dystrophie musculaire --- r_associated #0: 10 --> en:roberts syndrome
    n1=dystrophie musculaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1646. déficit en phosphatases alcalines --- r_associated #0: 10 --> en:roberts syndrome
    n1=déficit en phosphatases alcalines | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1647. déficit intellectuel --- r_associated #0: 10 --> en:roberts syndrome
    n1=déficit intellectuel | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1648. ectodermitis erosiva pluriorificialis --- r_associated #0: 10 --> en:roberts syndrome
    n1=ectodermitis erosiva pluriorificialis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1649. ectodermose --- r_associated #0: 10 --> en:roberts syndrome
    n1=ectodermose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1650. ectodermose érosive pluriorificielle de Fiessinger-Rendu --- r_associated #0: 10 --> en:roberts syndrome
    n1=ectodermose érosive pluriorificielle de Fiessinger-Rendu | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1651. ectoenzyme --- r_associated #0: 10 --> en:roberts syndrome
    n1=ectoenzyme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1652. ectomie --- r_associated #0: 10 --> en:roberts syndrome
    n1=ectomie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1653. ectomorphie --- r_associated #0: 10 --> en:roberts syndrome
    n1=ectomorphie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1654. ectoparasite --- r_associated #0: 10 --> en:roberts syndrome
    n1=ectoparasite | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1655. ectoparasitose --- r_associated #0: 10 --> en:roberts syndrome
    n1=ectoparasitose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1656. ectopie cardiaque --- r_associated #0: 10 --> en:roberts syndrome
    n1=ectopie cardiaque | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1657. ectopie des procès ciliaires --- r_associated #0: 10 --> en:roberts syndrome
    n1=ectopie des procès ciliaires | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1658. ectopie du cristallin --- r_associated #0: 10 --> en:roberts syndrome
    n1=ectopie du cristallin | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1659. en:5p minus syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:5p minus syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1660. en:5q microdeletion --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:5q microdeletion | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1661. en:Albert's position --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Albert's position | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1662. en:Albright's hereditary osteodystrophy --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Albright's hereditary osteodystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1663. en:Arrhenius'law --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Arrhenius'law | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1664. en:Bracht's manoeuvre --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Bracht's manoeuvre | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1665. en:Cogan-Reese syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Cogan-Reese syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1666. en:Crouzon's disease --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Crouzon's disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1667. en:Crouzon?s disease --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Crouzon?s disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1668. en:Down's --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Down's | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1669. en:Down's syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Down's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1670. en:FrontoMetaphyseal Dysplasia --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:FrontoMetaphyseal Dysplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1671. en:Holt-Oram syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Holt-Oram syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1672. en:Jadassohn-Lewandowsky syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Jadassohn-Lewandowsky syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1673. en:Korsakoff''s syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Korsakoff''s syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1674. en:Korsakoff's syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Korsakoff's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1675. en:LEOPARD syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:LEOPARD syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1676. en:Lejeune's syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Lejeune's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1677. en:MELAS syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:MELAS syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1678. en:NHSA III --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:NHSA III | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1679. en:PWS --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:PWS | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1680. en:Perthes' disease --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Perthes' disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1681. en:Riley-Day's syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Riley-Day's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1682. en:Schmorl's jaundice --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Schmorl's jaundice | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1683. en:Schridde's disease --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Schridde's disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1684. en:Shy-Drager's syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Shy-Drager's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1685. en:Smith-Magenis syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Smith-Magenis syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1686. en:Sotos's syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Sotos's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1687. en:Stilling-Türk-Duane's syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Stilling-Türk-Duane's syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1688. en:Tay Sachs' disease --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Tay Sachs' disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1689. en:WBS --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:WBS | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1690. en:Williams' syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Williams' syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1691. en:Williams-Beuren syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:Williams-Beuren syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1692. en:abdominal wall aplasia --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:abdominal wall aplasia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1693. en:acquired immune deficiency syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:acquired immune deficiency syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1694. en:acromegalia --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:acromegalia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1695. en:adactylia --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:adactylia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1696. en:alcaptonuria --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:alcaptonuria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1697. en:anaesthesia for porphyria --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:anaesthesia for porphyria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1698. en:and growth retardation --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:and growth retardation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1699. en:and oligophrenia --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:and oligophrenia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1700. en:and photophobia syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:and photophobia syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1701. en:and postaxil polydactylie --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:and postaxil polydactylie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1702. en:and sensorineural deafness --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:and sensorineural deafness | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1703. en:atresia ani --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:atresia ani | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1704. en:atrichia --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:atrichia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1705. en:bilirubin encephalopathy --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:bilirubin encephalopathy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1706. en:bony frailty with craniostenosis --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:bony frailty with craniostenosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1707. en:brachydactylia --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:brachydactylia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1708. en:cancrum oris --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:cancrum oris | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1709. en:cat cry disease --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:cat cry disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1710. en:cat cry syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:cat cry syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1711. en:chromosome 5p deletion syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:chromosome 5p deletion syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1712. en:congenital insensitivity to pain type III --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:congenital insensitivity to pain type III | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1713. en:ectrodactyly and macular dystrophy --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:ectrodactyly and macular dystrophy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1714. en:eds --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:eds | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1715. en:ehlers danlos syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:ehlers danlos syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1716. en:endocrine disorder --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:endocrine disorder | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1717. en:erythroblastosis fetalis --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:erythroblastosis fetalis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1718. en:eye abnormality --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:eye abnormality | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1719. en:facial clefting syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:facial clefting syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1720. en:follicularis --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:follicularis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1721. en:glycogenosis --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:glycogenosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1722. en:green monkey virus disease --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:green monkey virus disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1723. en:hereditary sensory and autonomic neuropathy type III --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:hereditary sensory and autonomic neuropathy type III | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1724. en:homogentisuria --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:homogentisuria | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1725. en:hydranencephaly --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:hydranencephaly | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1726. en:hypospadias --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:hypospadias | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1727. en:hypoxemia --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:hypoxemia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1728. en:infectious gangrene of the mouth --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:infectious gangrene of the mouth | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1729. en:intellectual disability --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:intellectual disability | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1730. en:interatrial septal defect --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:interatrial septal defect | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1731. en:interventricular septal defect --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:interventricular septal defect | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1732. en:intestinal malabsorption --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:intestinal malabsorption | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1733. en:irideremia --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:irideremia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1734. en:iris coloboma with ptosis --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:iris coloboma with ptosis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1735. en:leper house --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:leper house | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1736. en:microtia --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:microtia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1737. en:minimal pigment type --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:minimal pigment type | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1738. en:myopia --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:myopia | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1739. en:nuclear icterus --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:nuclear icterus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1740. en:nuclear jaundice --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:nuclear jaundice | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1741. en:optic neuropathy --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:optic neuropathy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1742. en:patterson-kelly syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:patterson-kelly syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1743. en:peripheral neuropathy in cold agglutinin disease --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:peripheral neuropathy in cold agglutinin disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1744. en:polysyndactyly syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:polysyndactyly syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1745. en:right sacrum anterior position --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:right sacrum anterior position | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1746. en:secundum defect --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:secundum defect | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1747. en:sign of the iceberg --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:sign of the iceberg | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1748. en:sinus venosus defect --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:sinus venosus defect | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1749. en:spastic neurologic disorder --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:spastic neurologic disorder | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1750. en:stress cardiomyopathy --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:stress cardiomyopathy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1751. en:substance withdrawal syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:substance withdrawal syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1752. en:surgical treatment of hydrocele --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:surgical treatment of hydrocele | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1753. en:trisomy 21 --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:trisomy 21 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1754. en:type 1 --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:type 1 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1755. en:type 2 --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:type 2 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1756. en:type 3 --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:type 3 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1757. en:type 4 --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:type 4 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1758. en:unusual facies --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:unusual facies | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1759. en:water on the brain --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:water on the brain | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1760. en:weaning syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:weaning syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1761. en:withdrawal syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:withdrawal syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1762. en:xanthine lithiasis --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:xanthine lithiasis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1763. en:xanthonychia syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:xanthonychia syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1764. en:xanthonychie --- r_associated #0: 10 --> en:roberts syndrome
    n1=en:xanthonychie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1765. encéphalocèle --- r_associated #0: 10 --> en:roberts syndrome
    n1=encéphalocèle | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1766. faciale (paralysie du nouveau-né) --- r_associated #0: 10 --> en:roberts syndrome
    n1=faciale (paralysie du nouveau-né) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1767. fente nasolabiopalatine --- r_associated #0: 10 --> en:roberts syndrome
    n1=fente nasolabiopalatine | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1768. fragilité osseuse avec craniosynostose, exophtalmie, hydrocéphalie et faciès caractéristique; --- r_associated #0: 10 --> en:roberts syndrome
    n1=fragilité osseuse avec craniosynostose, exophtalmie, hydrocéphalie et faciès caractéristique; | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1769. gastroschisis --- r_associated #0: 10 --> en:roberts syndrome
    n1=gastroschisis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1770. genu varum --- r_associated #0: 10 --> en:roberts syndrome
    n1=genu varum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1771. glaucome capsulaire --- r_associated #0: 10 --> en:roberts syndrome
    n1=glaucome capsulaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1772. glycogénique (surcharge et infiltration) --- r_associated #0: 10 --> en:roberts syndrome
    n1=glycogénique (surcharge et infiltration) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1773. hernie diaphragmatique --- r_associated #0: 10 --> en:roberts syndrome
    n1=hernie diaphragmatique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1774. holocentromère --- r_associated #0: 10 --> en:roberts syndrome
    n1=holocentromère | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1775. holocentromérique --- r_associated #0: 10 --> en:roberts syndrome
    n1=holocentromérique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1776. holocrine --- r_associated #0: 10 --> en:roberts syndrome
    n1=holocrine | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1777. holodiastolique --- r_associated #0: 10 --> en:roberts syndrome
    n1=holodiastolique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1778. holoenzyme --- r_associated #0: 10 --> en:roberts syndrome
    n1=holoenzyme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1779. hologamie --- r_associated #0: 10 --> en:roberts syndrome
    n1=hologamie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1780. hologynique --- r_associated #0: 10 --> en:roberts syndrome
    n1=hologynique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1781. holomérocrine --- r_associated #0: 10 --> en:roberts syndrome
    n1=holomérocrine | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1782. holophrase --- r_associated #0: 10 --> en:roberts syndrome
    n1=holophrase | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1783. holoproencéphalie --- r_associated #0: 10 --> en:roberts syndrome
    n1=holoproencéphalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1784. hydramnios aigu --- r_associated #0: 10 --> en:roberts syndrome
    n1=hydramnios aigu | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1785. hydramnios chronique --- r_associated #0: 10 --> en:roberts syndrome
    n1=hydramnios chronique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1786. hydrargirose --- r_associated #0: 10 --> en:roberts syndrome
    n1=hydrargirose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1787. hydrargyrisme --- r_associated #0: 10 --> en:roberts syndrome
    n1=hydrargyrisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1788. hydratase --- r_associated #0: 10 --> en:roberts syndrome
    n1=hydratase | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1789. hydratation cutanée --- r_associated #0: 10 --> en:roberts syndrome
    n1=hydratation cutanée | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1790. hydrate de carbone --- r_associated #0: 10 --> en:roberts syndrome
    n1=hydrate de carbone | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1791. hydrencéphalocèle --- r_associated #0: 10 --> en:roberts syndrome
    n1=hydrencéphalocèle | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1792. hydrine --- r_associated #0: 10 --> en:roberts syndrome
    n1=hydrine | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1793. hydroa --- r_associated #0: 10 --> en:roberts syndrome
    n1=hydroa | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1794. hydroa aestivalis --- r_associated #0: 10 --> en:roberts syndrome
    n1=hydroa aestivalis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1795. hydrocephalus --- r_associated #0: 10 --> en:roberts syndrome
    n1=hydrocephalus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1796. hypertensinase --- r_associated #0: 10 --> en:roberts syndrome
    n1=hypertensinase | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1797. hypertensine --- r_associated #0: 10 --> en:roberts syndrome
    n1=hypertensine | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1798. hypertensinogène --- r_associated #0: 10 --> en:roberts syndrome
    n1=hypertensinogène | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1799. hypertension --- r_associated #0: 10 --> en:roberts syndrome
    n1=hypertension | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1800. hypertension abdominale --- r_associated #0: 10 --> en:roberts syndrome
    n1=hypertension abdominale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1801. hypertension artérielle --- r_associated #0: 10 --> en:roberts syndrome
    n1=hypertension artérielle | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1802. hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental --- r_associated #0: 10 --> en:roberts syndrome
    n1=hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1803. hypohypophysie --- r_associated #0: 10 --> en:roberts syndrome
    n1=hypohypophysie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1804. hypophosphatasies --- r_associated #0: 10 --> en:roberts syndrome
    n1=hypophosphatasies | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1805. hypostimulinie --- r_associated #0: 10 --> en:roberts syndrome
    n1=hypostimulinie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1806. hémochromatose primitive --- r_associated #0: 10 --> en:roberts syndrome
    n1=hémochromatose primitive | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1807. impédance acoustique (symb. Z) --- r_associated #0: 10 --> en:roberts syndrome
    n1=impédance acoustique (symb. Z) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1808. incontinentia pigmenti --- r_associated #0: 10 --> en:roberts syndrome
    n1=incontinentia pigmenti | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1809. laparoschisis --- r_associated #0: 10 --> en:roberts syndrome
    n1=laparoschisis | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1810. maladie de Duhring --- r_associated #0: 10 --> en:roberts syndrome
    n1=maladie de Duhring | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1811. maladie de Gilles de la Tourette --- r_associated #0: 10 --> en:roberts syndrome
    n1=maladie de Gilles de la Tourette | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1812. maladie de Stargardt --- r_associated #0: 10 --> en:roberts syndrome
    n1=maladie de Stargardt | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1813. maladie de Tangier --- r_associated #0: 10 --> en:roberts syndrome
    n1=maladie de Tangier | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1814. maladie des tics --- r_associated #0: 10 --> en:roberts syndrome
    n1=maladie des tics | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1815. maladie des tics de Gilles de la Tourette --- r_associated #0: 10 --> en:roberts syndrome
    n1=maladie des tics de Gilles de la Tourette | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1816. maladies de gilles de la tourette --- r_associated #0: 10 --> en:roberts syndrome
    n1=maladies de gilles de la tourette | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1817. micrognatisme --- r_associated #0: 10 --> en:roberts syndrome
    n1=micrognatisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1818. microgéodes phalangiennes (syndrome des) --- r_associated #0: 10 --> en:roberts syndrome
    n1=microgéodes phalangiennes (syndrome des) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1819. mort imminente (expérience de la) --- r_associated #0: 10 --> en:roberts syndrome
    n1=mort imminente (expérience de la) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1820. nanisme --- r_associated #0: 10 --> en:roberts syndrome
    n1=nanisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1821. neuroblastome (mise en évidence scintigraphique du) --- r_associated #0: 10 --> en:roberts syndrome
    n1=neuroblastome (mise en évidence scintigraphique du) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1822. néphritique (syndrome) --- r_associated #0: 10 --> en:roberts syndrome
    n1=néphritique (syndrome) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1823. omphalocèle --- r_associated #0: 10 --> en:roberts syndrome
    n1=omphalocèle | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1824. ostéoporose-pseudogliome (syndrome) --- r_associated #0: 10 --> en:roberts syndrome
    n1=ostéoporose-pseudogliome (syndrome) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1825. paralysie périodique hypokaliémique familiale (maladie de Westphal) --- r_associated #0: 10 --> en:roberts syndrome
    n1=paralysie périodique hypokaliémique familiale (maladie de Westphal) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1826. paraplégie spastique dans la syphilis congénitale --- r_associated #0: 10 --> en:roberts syndrome
    n1=paraplégie spastique dans la syphilis congénitale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1827. pinta --- r_associated #0: 10 --> en:roberts syndrome
    n1=pinta | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1828. pluripotence --- r_associated #0: 10 --> en:roberts syndrome
    n1=pluripotence | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1829. pluripotent --- r_associated #0: 10 --> en:roberts syndrome
    n1=pluripotent | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1830. plurisegmentectomie hépatique --- r_associated #0: 10 --> en:roberts syndrome
    n1=plurisegmentectomie hépatique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1831. pneumallergène --- r_associated #0: 10 --> en:roberts syndrome
    n1=pneumallergène | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1832. pneumatisation de l'apophyse unciforme --- r_associated #0: 10 --> en:roberts syndrome
    n1=pneumatisation de l'apophyse unciforme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1833. pneumatisation du cornet moyen --- r_associated #0: 10 --> en:roberts syndrome
    n1=pneumatisation du cornet moyen | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1834. pneumatocèle --- r_associated #0: 10 --> en:roberts syndrome
    n1=pneumatocèle | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1835. pneumatose colique --- r_associated #0: 10 --> en:roberts syndrome
    n1=pneumatose colique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1836. pneumaturie --- r_associated #0: 10 --> en:roberts syndrome
    n1=pneumaturie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1837. pneumectomie --- r_associated #0: 10 --> en:roberts syndrome
    n1=pneumectomie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1838. pneumoarthrographie --- r_associated #0: 10 --> en:roberts syndrome
    n1=pneumoarthrographie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1839. pneumobilie --- r_associated #0: 10 --> en:roberts syndrome
    n1=pneumobilie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1840. polyglucosanes (neuropathie à ) --- r_associated #0: 10 --> en:roberts syndrome
    n1=polyglucosanes (neuropathie à ) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1841. polymyalgia rheumatica --- r_associated #0: 10 --> en:roberts syndrome
    n1=polymyalgia rheumatica | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1842. poumon (fonctions métaboliques du) --- r_associated #0: 10 --> en:roberts syndrome
    n1=poumon (fonctions métaboliques du) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1843. profondeur de l'anesthésie (stade de) --- r_associated #0: 10 --> en:roberts syndrome
    n1=profondeur de l'anesthésie (stade de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1844. prolidase (déficit en) --- r_associated #0: 10 --> en:roberts syndrome
    n1=prolidase (déficit en) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1845. protéine trifonctionnelle mitochondriale (déficit en) --- r_associated #0: 10 --> en:roberts syndrome
    n1=protéine trifonctionnelle mitochondriale (déficit en) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1846. pseudo-hypoaldostéronisme --- r_associated #0: 10 --> en:roberts syndrome
    n1=pseudo-hypoaldostéronisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1847. pseudohypoaldostéronisme --- r_associated #0: 10 --> en:roberts syndrome
    n1=pseudohypoaldostéronisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1848. quadriplégie spastique, rétinite pigmentaire et retard mental --- r_associated #0: 10 --> en:roberts syndrome
    n1=quadriplégie spastique, rétinite pigmentaire et retard mental | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1849. rate aberrante --- r_associated #0: 10 --> en:roberts syndrome
    n1=rate aberrante | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1850. rate flottante --- r_associated #0: 10 --> en:roberts syndrome
    n1=rate flottante | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1851. rate vagabonde --- r_associated #0: 10 --> en:roberts syndrome
    n1=rate vagabonde | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1852. rétinite pigmentaire et retard mental --- r_associated #0: 10 --> en:roberts syndrome
    n1=rétinite pigmentaire et retard mental | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1853. rétinite pigmentaire, surdité, retard mental, et hypogonadisme --- r_associated #0: 10 --> en:roberts syndrome
    n1=rétinite pigmentaire, surdité, retard mental, et hypogonadisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1854. seitelberger --- r_associated #0: 10 --> en:roberts syndrome
    n1=seitelberger | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1855. sel biliaire --- r_associated #0: 10 --> en:roberts syndrome
    n1=sel biliaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1856. sirtuine --- r_associated #0: 10 --> en:roberts syndrome
    n1=sirtuine | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1857. sisi-test --- r_associated #0: 10 --> en:roberts syndrome
    n1=sisi-test | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1858. sismothérapie --- r_associated #0: 10 --> en:roberts syndrome
    n1=sismothérapie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1859. situs inversus viscerum --- r_associated #0: 10 --> en:roberts syndrome
    n1=situs inversus viscerum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1860. situs mutatus --- r_associated #0: 10 --> en:roberts syndrome
    n1=situs mutatus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1861. souche de référence --- r_associated #0: 10 --> en:roberts syndrome
    n1=souche de référence | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1862. souche transduite --- r_associated #0: 10 --> en:roberts syndrome
    n1=souche transduite | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1863. splénoptose --- r_associated #0: 10 --> en:roberts syndrome
    n1=splénoptose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1864. stiff skin syndrome --- r_associated #0: 10 --> en:roberts syndrome
    n1=stiff skin syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1865. surdité --- r_associated #0: 10 --> en:roberts syndrome
    n1=surdité | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1866. syndrome cataracte-ataxie-surdité et retard mental --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome cataracte-ataxie-surdité et retard mental | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1867. syndrome de Duker-Weiss-Siber --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de Duker-Weiss-Siber | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1868. syndrome de Feingold --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de Feingold | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1869. syndrome de Gilles de la Tourette --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de Gilles de la Tourette | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1870. syndrome de Leriche --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de Leriche | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1871. syndrome de Mayer-Rokitansky-Küster-Hauser --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de Mayer-Rokitansky-Küster-Hauser | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1872. syndrome de Rathbun --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de Rathbun | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1873. syndrome de Rokitansky --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de Rokitansky | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1874. syndrome de Rokitansky-Küster-Hauser --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de Rokitansky-Küster-Hauser | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1875. syndrome de Stein-Leventhal-Cohen --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de Stein-Leventhal-Cohen | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1876. syndrome de Stevens-Johnson --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de Stevens-Johnson | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1877. syndrome de Townes-Brocks --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de Townes-Brocks | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1878. syndrome de Treft-Sanborn-Carey --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de Treft-Sanborn-Carey | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1879. syndrome de de Morsier --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de de Morsier | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1880. syndrome de la Tourette --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de la Tourette | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1881. syndrome de sheehan --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de sheehan | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1882. syndrome de stress respiratoire de l'adulte --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de stress respiratoire de l'adulte | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1883. syndrome de tourette --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de tourette | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1884. syndrome de zellweger --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome de zellweger | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1885. syndrome des pouces en adduction-arthrogrypose (type Dundar) --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome des pouces en adduction-arthrogrypose (type Dundar) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1886. syndrome des tics de Gilles de la Tourette --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome des tics de Gilles de la Tourette | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1887. syndrome du p(17)p11.2p11.2 --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome du p(17)p11.2p11.2 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1888. syndrome malin d'un neuroleptique --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome malin d'un neuroleptique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1889. syndrome malin de neuroleptiques --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome malin de neuroleptiques | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1890. syndrome malin des neuroleptiques --- r_associated #0: 10 --> en:roberts syndrome
    n1=syndrome malin des neuroleptiques | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1891. sélacien venimeux --- r_associated #0: 10 --> en:roberts syndrome
    n1=sélacien venimeux | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1892. toxémie --- r_associated #0: 10 --> en:roberts syndrome
    n1=toxémie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1893. trichomégalie avec retard mental, nanisme, et dégénérescence pigmentée de la rétine --- r_associated #0: 10 --> en:roberts syndrome
    n1=trichomégalie avec retard mental, nanisme, et dégénérescence pigmentée de la rétine | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1894. triphosphopyridine-nucléotide --- r_associated #0: 10 --> en:roberts syndrome
    n1=triphosphopyridine-nucléotide | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1895. trisomie 9p --- r_associated #0: 10 --> en:roberts syndrome
    n1=trisomie 9p | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1896. trouble de gilles de la tourette --- r_associated #0: 10 --> en:roberts syndrome
    n1=trouble de gilles de la tourette | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1897. télécardiographie --- r_associated #0: 10 --> en:roberts syndrome
    n1=télécardiographie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1898. télécardiophone --- r_associated #0: 10 --> en:roberts syndrome
    n1=télécardiophone | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1899. téléclitoridie --- r_associated #0: 10 --> en:roberts syndrome
    n1=téléclitoridie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1900. télécobalt --- r_associated #0: 10 --> en:roberts syndrome
    n1=télécobalt | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1901. télécobalt-thérapie --- r_associated #0: 10 --> en:roberts syndrome
    n1=télécobalt-thérapie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1902. téléconsultation --- r_associated #0: 10 --> en:roberts syndrome
    n1=téléconsultation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1903. télécrâne --- r_associated #0: 10 --> en:roberts syndrome
    n1=télécrâne | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1904. télécæsiothérapie --- r_associated #0: 10 --> en:roberts syndrome
    n1=télécæsiothérapie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1905. télédermatologie --- r_associated #0: 10 --> en:roberts syndrome
    n1=télédermatologie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1906. télédiastole --- r_associated #0: 10 --> en:roberts syndrome
    n1=télédiastole | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1907. télédétection --- r_associated #0: 10 --> en:roberts syndrome
    n1=télédétection | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1908. urticaire-surdité-amylose rénale --- r_associated #0: 10 --> en:roberts syndrome
    n1=urticaire-surdité-amylose rénale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1909. varicelle (complications neurologiques de la) --- r_associated #0: 10 --> en:roberts syndrome
    n1=varicelle (complications neurologiques de la) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1910. état de mal épileptique --- r_associated #0: 10 --> en:roberts syndrome
    n1=état de mal épileptique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=10
  1911. dysencéphalie splanchnokystique --- r_associated #0: 6 --> en:roberts syndrome
    n1=dysencéphalie splanchnokystique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=6
  1912. trisomie 13 --- r_associated #0: 6 --> en:roberts syndrome
    n1=trisomie 13 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=6
  1913. trisomie 18 --- r_associated #0: 6 --> en:roberts syndrome
    n1=trisomie 18 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=6
  1914. ARRX --- r_associated #0: 5 --> en:roberts syndrome
    n1=ARRX | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1915. Acinetobacter --- r_associated #0: 5 --> en:roberts syndrome
    n1=Acinetobacter | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1916. Adair-Dighton (syndrome d') --- r_associated #0: 5 --> en:roberts syndrome
    n1=Adair-Dighton (syndrome d') | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1917. Alagille (syndrome d') --- r_associated #0: 5 --> en:roberts syndrome
    n1=Alagille (syndrome d') | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1918. Anasarque --- r_associated #0: 5 --> en:roberts syndrome
    n1=Anasarque | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1919. Dumoulin (classification de) --- r_associated #0: 5 --> en:roberts syndrome
    n1=Dumoulin (classification de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1920. Handicap mental --- r_associated #0: 5 --> en:roberts syndrome
    n1=Handicap mental | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1921. Korsakoff (syndrome de) --- r_associated #0: 5 --> en:roberts syndrome
    n1=Korsakoff (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1922. Li-Fraumeni (syndrome de) --- r_associated #0: 5 --> en:roberts syndrome
    n1=Li-Fraumeni (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1923. Maladie du cri du chat --- r_associated #0: 5 --> en:roberts syndrome
    n1=Maladie du cri du chat | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1924. Neurocysticercose --- r_associated #0: 5 --> en:roberts syndrome
    n1=Neurocysticercose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1925. Neuropathie optique --- r_associated #0: 5 --> en:roberts syndrome
    n1=Neuropathie optique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1926. Onsager (relation d') --- r_associated #0: 5 --> en:roberts syndrome
    n1=Onsager (relation d') | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1927. Perthes (maladie de) --- r_associated #0: 5 --> en:roberts syndrome
    n1=Perthes (maladie de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1928. Peste Noire --- r_associated #0: 5 --> en:roberts syndrome
    n1=Peste Noire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1929. Syndrome d'Immunodéficience Acquise --- r_associated #0: 5 --> en:roberts syndrome
    n1=Syndrome d'Immunodéficience Acquise | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1930. Tay-Sachs (maladie de) --- r_associated #0: 5 --> en:roberts syndrome
    n1=Tay-Sachs (maladie de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1931. Williams (syndrome de) --- r_associated #0: 5 --> en:roberts syndrome
    n1=Williams (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1932. abêtalipoprotéinémie --- r_associated #0: 5 --> en:roberts syndrome
    n1=abêtalipoprotéinémie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1933. acidurie --- r_associated #0: 5 --> en:roberts syndrome
    n1=acidurie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1934. acidurie 3-hydroxy-3-méthyl-glutarique --- r_associated #0: 5 --> en:roberts syndrome
    n1=acidurie 3-hydroxy-3-méthyl-glutarique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1935. acidurie 3-méthylglutaconique --- r_associated #0: 5 --> en:roberts syndrome
    n1=acidurie 3-méthylglutaconique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1936. acidurie 4-hydroxybutyrique --- r_associated #0: 5 --> en:roberts syndrome
    n1=acidurie 4-hydroxybutyrique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1937. acidurie paradoxale --- r_associated #0: 5 --> en:roberts syndrome
    n1=acidurie paradoxale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1938. acineux --- r_associated #0: 5 --> en:roberts syndrome
    n1=acineux | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1939. acini --- r_associated #0: 5 --> en:roberts syndrome
    n1=acini | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1940. acinus --- r_associated #0: 5 --> en:roberts syndrome
    n1=acinus | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1941. acinus hépatique de Rappaport --- r_associated #0: 5 --> en:roberts syndrome
    n1=acinus hépatique de Rappaport | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1942. agglutinines irrégulières --- r_associated #0: 5 --> en:roberts syndrome
    n1=agglutinines irrégulières | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1943. agglutinogène --- r_associated #0: 5 --> en:roberts syndrome
    n1=agglutinogène | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1944. agitation postopératoire --- r_associated #0: 5 --> en:roberts syndrome
    n1=agitation postopératoire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1945. aglossie et adactylie --- r_associated #0: 5 --> en:roberts syndrome
    n1=aglossie et adactylie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1946. aglycone --- r_associated #0: 5 --> en:roberts syndrome
    n1=aglycone | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1947. agnosie chromatique --- r_associated #0: 5 --> en:roberts syndrome
    n1=agnosie chromatique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1948. agnosie d'extensité --- r_associated #0: 5 --> en:roberts syndrome
    n1=agnosie d'extensité | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1949. agnosie d'intensité --- r_associated #0: 5 --> en:roberts syndrome
    n1=agnosie d'intensité | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1950. agnosie des couleurs --- r_associated #0: 5 --> en:roberts syndrome
    n1=agnosie des couleurs | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1951. albinisme avec immunodéficience et troubles hématologiques --- r_associated #0: 5 --> en:roberts syndrome
    n1=albinisme avec immunodéficience et troubles hématologiques | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1952. albinisme avec surdité --- r_associated #0: 5 --> en:roberts syndrome
    n1=albinisme avec surdité | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1953. amnésie globale transitoire --- r_associated #0: 5 --> en:roberts syndrome
    n1=amnésie globale transitoire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1954. arrière-pied --- r_associated #0: 5 --> en:roberts syndrome
    n1=arrière-pied | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1955. brachy-oesophage --- r_associated #0: 5 --> en:roberts syndrome
    n1=brachy-oesophage | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1956. brachyclinodactylie --- r_associated #0: 5 --> en:roberts syndrome
    n1=brachyclinodactylie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1957. brachycères --- r_associated #0: 5 --> en:roberts syndrome
    n1=brachycères | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1958. brachycéphalie --- r_associated #0: 5 --> en:roberts syndrome
    n1=brachycéphalie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1959. cri du chat (maladie du) --- r_associated #0: 5 --> en:roberts syndrome
    n1=cri du chat (maladie du) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1960. disomie uniparentale --- r_associated #0: 5 --> en:roberts syndrome
    n1=disomie uniparentale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1961. duodénectomie --- r_associated #0: 5 --> en:roberts syndrome
    n1=duodénectomie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1962. duodénite --- r_associated #0: 5 --> en:roberts syndrome
    n1=duodénite | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1963. dysembryome cutané --- r_associated #0: 5 --> en:roberts syndrome
    n1=dysembryome cutané | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1964. dysembryome de l'ovaire --- r_associated #0: 5 --> en:roberts syndrome
    n1=dysembryome de l'ovaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1965. dysembryome testiculaire --- r_associated #0: 5 --> en:roberts syndrome
    n1=dysembryome testiculaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1966. dysembryoplasie --- r_associated #0: 5 --> en:roberts syndrome
    n1=dysembryoplasie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1967. dysembryoplasie neuro-épithéliale --- r_associated #0: 5 --> en:roberts syndrome
    n1=dysembryoplasie neuro-épithéliale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1968. dysenterie --- r_associated #0: 5 --> en:roberts syndrome
    n1=dysenterie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1969. dysenterie amibienne --- r_associated #0: 5 --> en:roberts syndrome
    n1=dysenterie amibienne | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1970. dysentériforme --- r_associated #0: 5 --> en:roberts syndrome
    n1=dysentériforme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1971. dysentérique --- r_associated #0: 5 --> en:roberts syndrome
    n1=dysentérique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1972. dysérythropoïèse --- r_associated #0: 5 --> en:roberts syndrome
    n1=dysérythropoïèse | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1973. démence d'Alzheimer --- r_associated #0: 5 --> en:roberts syndrome
    n1=démence d'Alzheimer | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1974. en:Neuroleptic malignant syndrome --- r_associated #0: 5 --> en:roberts syndrome
    n1=en:Neuroleptic malignant syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1975. en:PFIC11 --- r_associated #0: 5 --> en:roberts syndrome
    n1=en:PFIC11 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1976. en:Sachs' disease --- r_associated #0: 5 --> en:roberts syndrome
    n1=en:Sachs' disease | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1977. en:Seckel syndrome --- r_associated #0: 5 --> en:roberts syndrome
    n1=en:Seckel syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1978. en:cat's cry syndrome --- r_associated #0: 5 --> en:roberts syndrome
    n1=en:cat's cry syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1979. fibrose systémique néphrogénique --- r_associated #0: 5 --> en:roberts syndrome
    n1=fibrose systémique néphrogénique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1980. hydrargyrie --- r_associated #0: 5 --> en:roberts syndrome
    n1=hydrargyrie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1981. hydroadénome --- r_associated #0: 5 --> en:roberts syndrome
    n1=hydroadénome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1982. hydrocalice --- r_associated #0: 5 --> en:roberts syndrome
    n1=hydrocalice | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1983. hydrocarboné --- r_associated #0: 5 --> en:roberts syndrome
    n1=hydrocarboné | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1984. hydrocarbure --- r_associated #0: 5 --> en:roberts syndrome
    n1=hydrocarbure | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1985. hydrocèle de la femme --- r_associated #0: 5 --> en:roberts syndrome
    n1=hydrocèle de la femme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1986. hydrocèle de la vaginale --- r_associated #0: 5 --> en:roberts syndrome
    n1=hydrocèle de la vaginale | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1987. hydrocèle du canal de Nück --- r_associated #0: 5 --> en:roberts syndrome
    n1=hydrocèle du canal de Nück | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1988. hydrocèle du cou --- r_associated #0: 5 --> en:roberts syndrome
    n1=hydrocèle du cou | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1989. hypoxanthine-guanine-phosphoribosyl-transferase (déficit en) --- r_associated #0: 5 --> en:roberts syndrome
    n1=hypoxanthine-guanine-phosphoribosyl-transferase (déficit en) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1990. hémochromatose --- r_associated #0: 5 --> en:roberts syndrome
    n1=hémochromatose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1991. ichtyophtalmie --- r_associated #0: 5 --> en:roberts syndrome
    n1=ichtyophtalmie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1992. ichtyosarcotoxisme --- r_associated #0: 5 --> en:roberts syndrome
    n1=ichtyosarcotoxisme | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1993. insectes (allergie aux) --- r_associated #0: 5 --> en:roberts syndrome
    n1=insectes (allergie aux) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1994. malabsorption (syndrome de) --- r_associated #0: 5 --> en:roberts syndrome
    n1=malabsorption (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1995. maladie de Duhring-Brocq --- r_associated #0: 5 --> en:roberts syndrome
    n1=maladie de Duhring-Brocq | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1996. myopathie primitive progressive --- r_associated #0: 5 --> en:roberts syndrome
    n1=myopathie primitive progressive | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1997. mésentérite rétractile --- r_associated #0: 5 --> en:roberts syndrome
    n1=mésentérite rétractile | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1998. mésentérite sclérosante --- r_associated #0: 5 --> en:roberts syndrome
    n1=mésentérite sclérosante | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  1999. neurinome bilatéral du nerf cochléaire (VIII) --- r_associated #0: 5 --> en:roberts syndrome
    n1=neurinome bilatéral du nerf cochléaire (VIII) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2000. onychodysplasie --- r_associated #0: 5 --> en:roberts syndrome
    n1=onychodysplasie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2001. onychogryphose --- r_associated #0: 5 --> en:roberts syndrome
    n1=onychogryphose | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2002. onycholyse --- r_associated #0: 5 --> en:roberts syndrome
    n1=onycholyse | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2003. onycholyse candidosique --- r_associated #0: 5 --> en:roberts syndrome
    n1=onycholyse candidosique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2004. onycholyse semi-lunaire partielle --- r_associated #0: 5 --> en:roberts syndrome
    n1=onycholyse semi-lunaire partielle | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2005. onychomadèse --- r_associated #0: 5 --> en:roberts syndrome
    n1=onychomadèse | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2006. onychomatricome --- r_associated #0: 5 --> en:roberts syndrome
    n1=onychomatricome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2007. opération de Dunn --- r_associated #0: 5 --> en:roberts syndrome
    n1=opération de Dunn | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2008. osteopoecilie --- r_associated #0: 5 --> en:roberts syndrome
    n1=osteopoecilie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2009. paragnathe --- r_associated #0: 5 --> en:roberts syndrome
    n1=paragnathe | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2010. pemphigoïde muqueux bénin --- r_associated #0: 5 --> en:roberts syndrome
    n1=pemphigoïde muqueux bénin | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2011. porphyrie aigüe intermittente --- r_associated #0: 5 --> en:roberts syndrome
    n1=porphyrie aigüe intermittente | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2012. porphyrie cutanée --- r_associated #0: 5 --> en:roberts syndrome
    n1=porphyrie cutanée | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2013. porphyrie de Doss --- r_associated #0: 5 --> en:roberts syndrome
    n1=porphyrie de Doss | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2014. ptose splénique --- r_associated #0: 5 --> en:roberts syndrome
    n1=ptose splénique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2015. rate ectopique --- r_associated #0: 5 --> en:roberts syndrome
    n1=rate ectopique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2016. rate errante --- r_associated #0: 5 --> en:roberts syndrome
    n1=rate errante | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2017. sars --- r_associated #0: 5 --> en:roberts syndrome
    n1=sars | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2018. syndrome d'Ehlers-Danlos --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome d'Ehlers-Danlos | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2019. syndrome de Dunnigan --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de Dunnigan | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2020. syndrome de Kallmann --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de Kallmann | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2021. syndrome de Kaposi-Juliusberg --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de Kaposi-Juliusberg | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2022. syndrome de Kearns-Sayre --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de Kearns-Sayre | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2023. syndrome de Kleine-Levin --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de Kleine-Levin | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2024. syndrome de Klüver-Bucy --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de Klüver-Bucy | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2025. syndrome de Reye --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de Reye | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2026. syndrome de Stickler --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de Stickler | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2027. syndrome de Waterhouse-Friderichsen --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de Waterhouse-Friderichsen | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2028. syndrome de Wolff-Parkinson-White --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de Wolff-Parkinson-White | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2029. syndrome de fiessinger-leroy-reiter --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de fiessinger-leroy-reiter | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2030. syndrome de l'angle pontocérébelleux --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de l'angle pontocérébelleux | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2031. syndrome de l'apex orbitaire --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de l'apex orbitaire | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2032. syndrome de l'apophyse styloïde longue --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de l'apophyse styloïde longue | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2033. syndrome de reiter --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de reiter | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2034. syndrome de syndrome de Joubert-Boltshauser --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome de syndrome de Joubert-Boltshauser | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2035. syndrome olfacto-génital --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndrome olfacto-génital | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2036. syndromes du gène 1 de la tumeur de Wilms --- r_associated #0: 5 --> en:roberts syndrome
    n1=syndromes du gène 1 de la tumeur de Wilms | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2037. triplet (CGG) n --- r_associated #0: 5 --> en:roberts syndrome
    n1=triplet (CGG) n | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2038. trisomie 17p11.2 --- r_associated #0: 5 --> en:roberts syndrome
    n1=trisomie 17p11.2 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2039. trisomie 8 --- r_associated #0: 5 --> en:roberts syndrome
    n1=trisomie 8 | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2040. xanthoastrocytome pléomorphe --- r_associated #0: 5 --> en:roberts syndrome
    n1=xanthoastrocytome pléomorphe | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2041. xanthochromie --- r_associated #0: 5 --> en:roberts syndrome
    n1=xanthochromie | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2042. xanthochromie caroténique --- r_associated #0: 5 --> en:roberts syndrome
    n1=xanthochromie caroténique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2043. xanthoerythrodermia perstans --- r_associated #0: 5 --> en:roberts syndrome
    n1=xanthoerythrodermia perstans | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2044. xanthogranulome juvénile --- r_associated #0: 5 --> en:roberts syndrome
    n1=xanthogranulome juvénile | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2045. xanthogranulome nécrobiotique --- r_associated #0: 5 --> en:roberts syndrome
    n1=xanthogranulome nécrobiotique | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2046. xanthogranulome palpébral --- r_associated #0: 5 --> en:roberts syndrome
    n1=xanthogranulome palpébral | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2047. xanthohistiocytome --- r_associated #0: 5 --> en:roberts syndrome
    n1=xanthohistiocytome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2048. xanthoma disseminatum --- r_associated #0: 5 --> en:roberts syndrome
    n1=xanthoma disseminatum | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=5
  2049. xanthomatose --- r_associated #0: 5 --> en:roberts syndrome
    n1=xanthomatose | n2=en:roberts syndrome | 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