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'en:microvillus inclusion disease'
(id=6734874 ; fe=en:microvillus inclusion disease ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=19772 creation date=2017-06-22 touchdate=2025-08-14 00:15:41.000)
≈ 340 relations sortantes

  1. en:microvillus inclusion disease -- r_associated #0: 42 / 1 -> en:collagenous sprue
    n1=en:microvillus inclusion disease | n2=en:collagenous sprue | rel=r_associated | relid=0 | w=42
  2. en:microvillus inclusion disease -- r_associated #0: 39 / 0.929 -> en:congenital anomaly of esophagus
    n1=en:microvillus inclusion disease | n2=en:congenital anomaly of esophagus | rel=r_associated | relid=0 | w=39
  3. en:microvillus inclusion disease -- r_associated #0: 39 / 0.929 -> en:lactase deficiency (disorder)
    n1=en:microvillus inclusion disease | n2=en:lactase deficiency (disorder) | rel=r_associated | relid=0 | w=39
  4. en:microvillus inclusion disease -- r_associated #0: 39 / 0.929 -> en:small intestine atresia
    n1=en:microvillus inclusion disease | n2=en:small intestine atresia | rel=r_associated | relid=0 | w=39
  5. en:microvillus inclusion disease -- r_associated #0: 37 / 0.881 -> en:congenital hypothyroidism
    n1=en:microvillus inclusion disease | n2=en:congenital hypothyroidism | rel=r_associated | relid=0 | w=37
  6. en:microvillus inclusion disease -- r_associated #0: 37 / 0.881 -> en:congenital kidney disorder
    n1=en:microvillus inclusion disease | n2=en:congenital kidney disorder | rel=r_associated | relid=0 | w=37
  7. en:microvillus inclusion disease -- r_associated #0: 36 / 0.857 -> en:congenital duplication of appendix
    n1=en:microvillus inclusion disease | n2=en:congenital duplication of appendix | rel=r_associated | relid=0 | w=36
  8. en:microvillus inclusion disease -- r_associated #0: 35 / 0.833 -> en:barrett esophagus
    n1=en:microvillus inclusion disease | n2=en:barrett esophagus | rel=r_associated | relid=0 | w=35
  9. en:microvillus inclusion disease -- r_associated #0: 35 / 0.833 -> en:congenital nervous system disorder
    n1=en:microvillus inclusion disease | n2=en:congenital nervous system disorder | rel=r_associated | relid=0 | w=35
  10. en:microvillus inclusion disease -- r_associated #0: 35 / 0.833 -> en:short bowel syndrome
    n1=en:microvillus inclusion disease | n2=en:short bowel syndrome | rel=r_associated | relid=0 | w=35
  11. en:microvillus inclusion disease -- r_associated #0: 34 / 0.81 -> en:anorectal agenesis
    n1=en:microvillus inclusion disease | n2=en:anorectal agenesis | rel=r_associated | relid=0 | w=34
  12. en:microvillus inclusion disease -- r_associated #0: 34 / 0.81 -> en:familial adenomatous polyposis
    n1=en:microvillus inclusion disease | n2=en:familial adenomatous polyposis | rel=r_associated | relid=0 | w=34
  13. en:microvillus inclusion disease -- r_associated #0: 34 / 0.81 -> en:lactose intolerance
    n1=en:microvillus inclusion disease | n2=en:lactose intolerance | rel=r_associated | relid=0 | w=34
  14. en:microvillus inclusion disease -- r_associated #0: 34 / 0.81 -> en:neuronal intestinal dysplasia
    n1=en:microvillus inclusion disease | n2=en:neuronal intestinal dysplasia | rel=r_associated | relid=0 | w=34
  15. en:microvillus inclusion disease -- r_associated #0: 34 / 0.81 -> en:vitello-intestinal duct remnant
    n1=en:microvillus inclusion disease | n2=en:vitello-intestinal duct remnant | rel=r_associated | relid=0 | w=34
  16. en:microvillus inclusion disease -- r_associated #0: 32 / 0.762 -> en:duodenal atresia
    n1=en:microvillus inclusion disease | n2=en:duodenal atresia | rel=r_associated | relid=0 | w=32
  17. en:microvillus inclusion disease -- r_associated #0: 32 / 0.762 -> en:intestinal atresia
    n1=en:microvillus inclusion disease | n2=en:intestinal atresia | rel=r_associated | relid=0 | w=32
  18. en:microvillus inclusion disease -- r_associated #0: 32 / 0.762 -> en:intestinal disorders congenital
    n1=en:microvillus inclusion disease | n2=en:intestinal disorders congenital | rel=r_associated | relid=0 | w=32
  19. en:microvillus inclusion disease -- r_associated #0: 32 / 0.762 -> en:kallmann syndrome
    n1=en:microvillus inclusion disease | n2=en:kallmann syndrome | rel=r_associated | relid=0 | w=32
  20. en:microvillus inclusion disease -- r_associated #0: 32 / 0.762 -> en:other specified congenital malformations of digestive system
    n1=en:microvillus inclusion disease | n2=en:other specified congenital malformations of digestive system | rel=r_associated | relid=0 | w=32
  21. en:microvillus inclusion disease -- r_associated #0: 32 / 0.762 -> en:satoyoshi syndrome
    n1=en:microvillus inclusion disease | n2=en:satoyoshi syndrome | rel=r_associated | relid=0 | w=32
  22. en:microvillus inclusion disease -- r_associated #0: 31 / 0.738 -> en:autoimmune enteropathy
    n1=en:microvillus inclusion disease | n2=en:autoimmune enteropathy | rel=r_associated | relid=0 | w=31
  23. en:microvillus inclusion disease -- r_associated #0: 31 / 0.738 -> en:beckwith-wiedemann syndrome
    n1=en:microvillus inclusion disease | n2=en:beckwith-wiedemann syndrome | rel=r_associated | relid=0 | w=31
  24. en:microvillus inclusion disease -- r_associated #0: 31 / 0.738 -> en:blind loop syndrome
    n1=en:microvillus inclusion disease | n2=en:blind loop syndrome | rel=r_associated | relid=0 | w=31
  25. en:microvillus inclusion disease -- r_associated #0: 31 / 0.738 -> en:congenital disease of brain
    n1=en:microvillus inclusion disease | n2=en:congenital disease of brain | rel=r_associated | relid=0 | w=31
  26. en:microvillus inclusion disease -- r_associated #0: 31 / 0.738 -> en:congenital eye disorder
    n1=en:microvillus inclusion disease | n2=en:congenital eye disorder | rel=r_associated | relid=0 | w=31
  27. en:microvillus inclusion disease -- r_associated #0: 31 / 0.738 -> en:galactosemia
    n1=en:microvillus inclusion disease | n2=en:galactosemia | rel=r_associated | relid=0 | w=31
  28. en:microvillus inclusion disease -- r_associated #0: 31 / 0.738 -> en:intestinal malrotation
    n1=en:microvillus inclusion disease | n2=en:intestinal malrotation | rel=r_associated | relid=0 | w=31
  29. en:microvillus inclusion disease -- r_associated #0: 31 / 0.738 -> en:microcolon
    n1=en:microvillus inclusion disease | n2=en:microcolon | rel=r_associated | relid=0 | w=31
  30. en:microvillus inclusion disease -- r_associated #0: 31 / 0.738 -> en:microvillus
    n1=en:microvillus inclusion disease | n2=en:microvillus | rel=r_associated | relid=0 | w=31
  31. en:microvillus inclusion disease -- r_associated #0: 31 / 0.738 -> en:peutz-jeghers syndrome
    n1=en:microvillus inclusion disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  32. en:microvillus inclusion disease -- r_associated #0: 31 / 0.738 -> en:steatorrhea
    n1=en:microvillus inclusion disease | n2=en:steatorrhea | rel=r_associated | relid=0 | w=31
  33. en:microvillus inclusion disease -- r_associated #0: 31 / 0.738 -> en:tropical sprue
    n1=en:microvillus inclusion disease | n2=en:tropical sprue | rel=r_associated | relid=0 | w=31
  34. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:adrenocortical hypofunction, chronic primary congenital
    n1=en:microvillus inclusion disease | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30
  35. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:congenital anomaly of gastrointestinal tract
    n1=en:microvillus inclusion disease | n2=en:congenital anomaly of gastrointestinal tract | rel=r_associated | relid=0 | w=30
  36. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:congenital anomaly of intestinal tract
    n1=en:microvillus inclusion disease | n2=en:congenital anomaly of intestinal tract | rel=r_associated | relid=0 | w=30
  37. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:congenital end-plate acetylcholinesterase deficiency
    n1=en:microvillus inclusion disease | n2=en:congenital end-plate acetylcholinesterase deficiency | rel=r_associated | relid=0 | w=30
  38. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:congenital facial asymmetry
    n1=en:microvillus inclusion disease | n2=en:congenital facial asymmetry | rel=r_associated | relid=0 | w=30
  39. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:congenital factor ix deficiency without inhibitor
    n1=en:microvillus inclusion disease | n2=en:congenital factor ix deficiency without inhibitor | rel=r_associated | relid=0 | w=30
  40. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:congenital leptin deficiency
    n1=en:microvillus inclusion disease | n2=en:congenital leptin deficiency | rel=r_associated | relid=0 | w=30
  41. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:congenital oral/facial/cranial defect
    n1=en:microvillus inclusion disease | n2=en:congenital oral/facial/cranial defect | rel=r_associated | relid=0 | w=30
  42. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:congenital reproductive system disorder
    n1=en:microvillus inclusion disease | n2=en:congenital reproductive system disorder | rel=r_associated | relid=0 | w=30
  43. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:esophageal atresia
    n1=en:microvillus inclusion disease | n2=en:esophageal atresia | rel=r_associated | relid=0 | w=30
  44. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:parachute malformation of right atrioventricular valve
    n1=en:microvillus inclusion disease | n2=en:parachute malformation of right atrioventricular valve | rel=r_associated | relid=0 | w=30
  45. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:pernicious anemia
    n1=en:microvillus inclusion disease | n2=en:pernicious anemia | rel=r_associated | relid=0 | w=30
  46. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:postprocedural steatorrhea
    n1=en:microvillus inclusion disease | n2=en:postprocedural steatorrhea | rel=r_associated | relid=0 | w=30
  47. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:rotation of tooth
    n1=en:microvillus inclusion disease | n2=en:rotation of tooth | rel=r_associated | relid=0 | w=30
  48. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:small intestinal infarction
    n1=en:microvillus inclusion disease | n2=en:small intestinal infarction | rel=r_associated | relid=0 | w=30
  49. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:small intestine anastomotic leak
    n1=en:microvillus inclusion disease | n2=en:small intestine anastomotic leak | rel=r_associated | relid=0 | w=30
  50. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:transposition of intestine (disorder)
    n1=en:microvillus inclusion disease | n2=en:transposition of intestine (disorder) | rel=r_associated | relid=0 | w=30
  51. en:microvillus inclusion disease -- r_associated #0: 30 / 0.714 -> en:true cleft of common atrioventricular valve leaflet
    n1=en:microvillus inclusion disease | n2=en:true cleft of common atrioventricular valve leaflet | rel=r_associated | relid=0 | w=30
  52. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:celiac disease
    n1=en:microvillus inclusion disease | n2=en:celiac disease | rel=r_associated | relid=0 | w=29
  53. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:chronic diarrhea due to glucoamylase deficiency
    n1=en:microvillus inclusion disease | n2=en:chronic diarrhea due to glucoamylase deficiency | rel=r_associated | relid=0 | w=29
  54. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:chronic steatorrhea
    n1=en:microvillus inclusion disease | n2=en:chronic steatorrhea | rel=r_associated | relid=0 | w=29
  55. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:congenital brain damage
    n1=en:microvillus inclusion disease | n2=en:congenital brain damage | rel=r_associated | relid=0 | w=29
  56. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:congenital choroidal fold
    n1=en:microvillus inclusion disease | n2=en:congenital choroidal fold | rel=r_associated | relid=0 | w=29
  57. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:congenital exophthalmos
    n1=en:microvillus inclusion disease | n2=en:congenital exophthalmos | rel=r_associated | relid=0 | w=29
  58. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:congenital fibrinogen abnormality
    n1=en:microvillus inclusion disease | n2=en:congenital fibrinogen abnormality | rel=r_associated | relid=0 | w=29
  59. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:congenital pseudoporencephaly
    n1=en:microvillus inclusion disease | n2=en:congenital pseudoporencephaly | rel=r_associated | relid=0 | w=29
  60. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:congenital uremia
    n1=en:microvillus inclusion disease | n2=en:congenital uremia | rel=r_associated | relid=0 | w=29
  61. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:fetal congenital tumor causing disproportion
    n1=en:microvillus inclusion disease | n2=en:fetal congenital tumor causing disproportion | rel=r_associated | relid=0 | w=29
  62. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:hereditary hemorrhagic telangiectasia
    n1=en:microvillus inclusion disease | n2=en:hereditary hemorrhagic telangiectasia | rel=r_associated | relid=0 | w=29
  63. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:lymphangiectasis, intestinal
    n1=en:microvillus inclusion disease | n2=en:lymphangiectasis, intestinal | rel=r_associated | relid=0 | w=29
  64. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:other specified congenital malformations of upper alimentary tract
    n1=en:microvillus inclusion disease | n2=en:other specified congenital malformations of upper alimentary tract | rel=r_associated | relid=0 | w=29
  65. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:regional congenital anomaly
    n1=en:microvillus inclusion disease | n2=en:regional congenital anomaly | rel=r_associated | relid=0 | w=29
  66. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:small bowel bacterial overgrowth syndrome
    n1=en:microvillus inclusion disease | n2=en:small bowel bacterial overgrowth syndrome | rel=r_associated | relid=0 | w=29
  67. en:microvillus inclusion disease -- r_associated #0: 29 / 0.69 -> en:small bowel fistula
    n1=en:microvillus inclusion disease | n2=en:small bowel fistula | rel=r_associated | relid=0 | w=29
  68. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:congenital
    n1=en:microvillus inclusion disease | n2=en:congenital | rel=r_associated | relid=0 | w=28
  69. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:congenital biliary tract disorder
    n1=en:microvillus inclusion disease | n2=en:congenital biliary tract disorder | rel=r_associated | relid=0 | w=28
  70. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:congenital blepharophimosis of upper eyelid
    n1=en:microvillus inclusion disease | n2=en:congenital blepharophimosis of upper eyelid | rel=r_associated | relid=0 | w=28
  71. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:congenital claw toe
    n1=en:microvillus inclusion disease | n2=en:congenital claw toe | rel=r_associated | relid=0 | w=28
  72. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:congenital factor ix deficiency with inhibitor
    n1=en:microvillus inclusion disease | n2=en:congenital factor ix deficiency with inhibitor | rel=r_associated | relid=0 | w=28
  73. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:congenital methemoglobinemia
    n1=en:microvillus inclusion disease | n2=en:congenital methemoglobinemia | rel=r_associated | relid=0 | w=28
  74. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:congenital neurogenic ileus syndrome
    n1=en:microvillus inclusion disease | n2=en:congenital neurogenic ileus syndrome | rel=r_associated | relid=0 | w=28
  75. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:congenital plasminogen activator inhibitor deficiency type 1
    n1=en:microvillus inclusion disease | n2=en:congenital plasminogen activator inhibitor deficiency type 1 | rel=r_associated | relid=0 | w=28
  76. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:congenital skin contracture
    n1=en:microvillus inclusion disease | n2=en:congenital skin contracture | rel=r_associated | relid=0 | w=28
  77. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:congenital vascular disorder
    n1=en:microvillus inclusion disease | n2=en:congenital vascular disorder | rel=r_associated | relid=0 | w=28
  78. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:digeorge syndrome
    n1=en:microvillus inclusion disease | n2=en:digeorge syndrome | rel=r_associated | relid=0 | w=28
  79. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:disaccharide metabolism disorder
    n1=en:microvillus inclusion disease | n2=en:disaccharide metabolism disorder | rel=r_associated | relid=0 | w=28
  80. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:disorder of ileum
    n1=en:microvillus inclusion disease | n2=en:disorder of ileum | rel=r_associated | relid=0 | w=28
  81. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:gluten sensitivity
    n1=en:microvillus inclusion disease | n2=en:gluten sensitivity | rel=r_associated | relid=0 | w=28
  82. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:hereditary fructose intolerance
    n1=en:microvillus inclusion disease | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=28
  83. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:hiv enteropathy
    n1=en:microvillus inclusion disease | n2=en:hiv enteropathy | rel=r_associated | relid=0 | w=28
  84. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:imperforate anus
    n1=en:microvillus inclusion disease | n2=en:imperforate anus | rel=r_associated | relid=0 | w=28
  85. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:prader-willi syndrome
    n1=en:microvillus inclusion disease | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=28
  86. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:right atrial endocardial fibroelastosis
    n1=en:microvillus inclusion disease | n2=en:right atrial endocardial fibroelastosis | rel=r_associated | relid=0 | w=28
  87. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:small intestinal hamartoma
    n1=en:microvillus inclusion disease | n2=en:small intestinal hamartoma | rel=r_associated | relid=0 | w=28
  88. en:microvillus inclusion disease -- r_associated #0: 28 / 0.667 -> en:vitamin d-dependent rickets, type 2
    n1=en:microvillus inclusion disease | n2=en:vitamin d-dependent rickets, type 2 | rel=r_associated | relid=0 | w=28
  89. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:acquired acrodermatitis enteropathica
    n1=en:microvillus inclusion disease | n2=en:acquired acrodermatitis enteropathica | rel=r_associated | relid=0 | w=27
  90. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:congenital absence of alimentary tract
    n1=en:microvillus inclusion disease | n2=en:congenital absence of alimentary tract | rel=r_associated | relid=0 | w=27
  91. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:congenital blepharophimosis of lower eyelid
    n1=en:microvillus inclusion disease | n2=en:congenital blepharophimosis of lower eyelid | rel=r_associated | relid=0 | w=27
  92. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:congenital cardiovascular disorder
    n1=en:microvillus inclusion disease | n2=en:congenital cardiovascular disorder | rel=r_associated | relid=0 | w=27
  93. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:congenital constriction of pylorus
    n1=en:microvillus inclusion disease | n2=en:congenital constriction of pylorus | rel=r_associated | relid=0 | w=27
  94. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:congenital debility of fetus
    n1=en:microvillus inclusion disease | n2=en:congenital debility of fetus | rel=r_associated | relid=0 | w=27
  95. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:congenital dysarthria
    n1=en:microvillus inclusion disease | n2=en:congenital dysarthria | rel=r_associated | relid=0 | w=27
  96. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:congenital dysphasia
    n1=en:microvillus inclusion disease | n2=en:congenital dysphasia | rel=r_associated | relid=0 | w=27
  97. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:congenital factor ix deficiency variant
    n1=en:microvillus inclusion disease | n2=en:congenital factor ix deficiency variant | rel=r_associated | relid=0 | w=27
  98. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:congenital hepatic porphyria
    n1=en:microvillus inclusion disease | n2=en:congenital hepatic porphyria | rel=r_associated | relid=0 | w=27
  99. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:congenital intestinal malformation
    n1=en:microvillus inclusion disease | n2=en:congenital intestinal malformation | rel=r_associated | relid=0 | w=27
  100. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:enterokinase deficiency
    n1=en:microvillus inclusion disease | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=27
  101. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:focal segmental ischemia of small intestine
    n1=en:microvillus inclusion disease | n2=en:focal segmental ischemia of small intestine | rel=r_associated | relid=0 | w=27
  102. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:hirschsprung disease
    n1=en:microvillus inclusion disease | n2=en:hirschsprung disease | rel=r_associated | relid=0 | w=27
  103. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:large intestine atresia
    n1=en:microvillus inclusion disease | n2=en:large intestine atresia | rel=r_associated | relid=0 | w=27
  104. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:parachute malformation of common atrioventricular valve
    n1=en:microvillus inclusion disease | n2=en:parachute malformation of common atrioventricular valve | rel=r_associated | relid=0 | w=27
  105. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:preternatural anus
    n1=en:microvillus inclusion disease | n2=en:preternatural anus | rel=r_associated | relid=0 | w=27
  106. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:shortened trunk
    n1=en:microvillus inclusion disease | n2=en:shortened trunk | rel=r_associated | relid=0 | w=27
  107. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> en:sucrose intolerance
    n1=en:microvillus inclusion disease | n2=en:sucrose intolerance | rel=r_associated | relid=0 | w=27
  108. en:microvillus inclusion disease -- r_associated #0: 27 / 0.643 -> maladie
    n1=en:microvillus inclusion disease | n2=maladie | rel=r_associated | relid=0 | w=27
  109. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> anomalie congénitale
    n1=en:microvillus inclusion disease | n2=anomalie congénitale | rel=r_associated | relid=0 | w=26
  110. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:chromosome disorder
    n1=en:microvillus inclusion disease | n2=en:chromosome disorder | rel=r_associated | relid=0 | w=26
  111. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:congenital anomaly of salivary gland
    n1=en:microvillus inclusion disease | n2=en:congenital anomaly of salivary gland | rel=r_associated | relid=0 | w=26
  112. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:congenital blocked tear duct
    n1=en:microvillus inclusion disease | n2=en:congenital blocked tear duct | rel=r_associated | relid=0 | w=26
  113. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:congenital gastrointestinal-urinary tract fistula
    n1=en:microvillus inclusion disease | n2=en:congenital gastrointestinal-urinary tract fistula | rel=r_associated | relid=0 | w=26
  114. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:congenital malignant melanoma
    n1=en:microvillus inclusion disease | n2=en:congenital malignant melanoma | rel=r_associated | relid=0 | w=26
  115. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:congenital posterior subcapsular polar cataract
    n1=en:microvillus inclusion disease | n2=en:congenital posterior subcapsular polar cataract | rel=r_associated | relid=0 | w=26
  116. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:congenital retinoschisis
    n1=en:microvillus inclusion disease | n2=en:congenital retinoschisis | rel=r_associated | relid=0 | w=26
  117. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:congenital skeletal disorder
    n1=en:microvillus inclusion disease | n2=en:congenital skeletal disorder | rel=r_associated | relid=0 | w=26
  118. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:congenital sucrase-isomaltase deficiency
    n1=en:microvillus inclusion disease | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=26
  119. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:fordyce's disease
    n1=en:microvillus inclusion disease | n2=en:fordyce's disease | rel=r_associated | relid=0 | w=26
  120. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:mobile caecum syndrome
    n1=en:microvillus inclusion disease | n2=en:mobile caecum syndrome | rel=r_associated | relid=0 | w=26
  121. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:mouth abnormalities
    n1=en:microvillus inclusion disease | n2=en:mouth abnormalities | rel=r_associated | relid=0 | w=26
  122. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:post-gastrointestinal tract surgery malnutrition
    n1=en:microvillus inclusion disease | n2=en:post-gastrointestinal tract surgery malnutrition | rel=r_associated | relid=0 | w=26
  123. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:small bowel adhesions
    n1=en:microvillus inclusion disease | n2=en:small bowel adhesions | rel=r_associated | relid=0 | w=26
  124. en:microvillus inclusion disease -- r_associated #0: 26 / 0.619 -> en:truncal valve overriding ventricular septum
    n1=en:microvillus inclusion disease | n2=en:truncal valve overriding ventricular septum | rel=r_associated | relid=0 | w=26
  125. en:microvillus inclusion disease -- r_associated #0: 25 / 0.595 -> en:acrodermatitis enteropathica
    n1=en:microvillus inclusion disease | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=25
  126. en:microvillus inclusion disease -- r_associated #0: 25 / 0.595 -> en:acute pseudo-obstruction of small intestine
    n1=en:microvillus inclusion disease | n2=en:acute pseudo-obstruction of small intestine | rel=r_associated | relid=0 | w=25
  127. en:microvillus inclusion disease -- r_associated #0: 25 / 0.595 -> en:congenital connective tissue disorder
    n1=en:microvillus inclusion disease | n2=en:congenital connective tissue disorder | rel=r_associated | relid=0 | w=25
  128. en:microvillus inclusion disease -- r_associated #0: 25 / 0.595 -> en:congenital hydrocele
    n1=en:microvillus inclusion disease | n2=en:congenital hydrocele | rel=r_associated | relid=0 | w=25
  129. en:microvillus inclusion disease -- r_associated #0: 25 / 0.595 -> en:congenital intestinal obstruction
    n1=en:microvillus inclusion disease | n2=en:congenital intestinal obstruction | rel=r_associated | relid=0 | w=25
  130. en:microvillus inclusion disease -- r_associated #0: 25 / 0.595 -> en:congenital/genetic syndrome with poikiloderma
    n1=en:microvillus inclusion disease | n2=en:congenital/genetic syndrome with poikiloderma | rel=r_associated | relid=0 | w=25
  131. en:microvillus inclusion disease -- r_associated #0: 25 / 0.595 -> en:infection by diphyllobothrium pacificum
    n1=en:microvillus inclusion disease | n2=en:infection by diphyllobothrium pacificum | rel=r_associated | relid=0 | w=25
  132. en:microvillus inclusion disease -- r_associated #0: 25 / 0.595 -> en:parachute malformation of left atrioventricular valve
    n1=en:microvillus inclusion disease | n2=en:parachute malformation of left atrioventricular valve | rel=r_associated | relid=0 | w=25
  133. en:microvillus inclusion disease -- r_associated #0: 25 / 0.595 -> en:right atrial appendage absent
    n1=en:microvillus inclusion disease | n2=en:right atrial appendage absent | rel=r_associated | relid=0 | w=25
  134. en:microvillus inclusion disease -- r_associated #0: 24 / 0.571 -> en:congenital atrophy of left lobe of liver
    n1=en:microvillus inclusion disease | n2=en:congenital atrophy of left lobe of liver | rel=r_associated | relid=0 | w=24
  135. en:microvillus inclusion disease -- r_associated #0: 24 / 0.571 -> en:congenital ear disorder
    n1=en:microvillus inclusion disease | n2=en:congenital ear disorder | rel=r_associated | relid=0 | w=24
  136. en:microvillus inclusion disease -- r_associated #0: 24 / 0.571 -> en:congenital fecaliths
    n1=en:microvillus inclusion disease | n2=en:congenital fecaliths | rel=r_associated | relid=0 | w=24
  137. en:microvillus inclusion disease -- r_associated #0: 24 / 0.571 -> en:enterospasm
    n1=en:microvillus inclusion disease | n2=en:enterospasm | rel=r_associated | relid=0 | w=24
  138. en:microvillus inclusion disease -- r_associated #0: 24 / 0.571 -> en:extensive congenital erosions, vesicles and reticulate scarring
    n1=en:microvillus inclusion disease | n2=en:extensive congenital erosions, vesicles and reticulate scarring | rel=r_associated | relid=0 | w=24
  139. en:microvillus inclusion disease -- r_associated #0: 24 / 0.571 -> en:hutch diverticulum
    n1=en:microvillus inclusion disease | n2=en:hutch diverticulum | rel=r_associated | relid=0 | w=24
  140. en:microvillus inclusion disease -- r_associated #0: 24 / 0.571 -> en:persistent cloaca
    n1=en:microvillus inclusion disease | n2=en:persistent cloaca | rel=r_associated | relid=0 | w=24
  141. en:microvillus inclusion disease -- r_associated #0: 24 / 0.571 -> en:primary malabsorption of infancy
    n1=en:microvillus inclusion disease | n2=en:primary malabsorption of infancy | rel=r_associated | relid=0 | w=24
  142. en:microvillus inclusion disease -- r_associated #0: 24 / 0.571 -> en:right atrial appendage - left - juxtaposition
    n1=en:microvillus inclusion disease | n2=en:right atrial appendage - left - juxtaposition | rel=r_associated | relid=0 | w=24
  143. en:microvillus inclusion disease -- r_associated #0: 23 / 0.548 -> en:cap myopathy
    n1=en:microvillus inclusion disease | n2=en:cap myopathy | rel=r_associated | relid=0 | w=23
  144. en:microvillus inclusion disease -- r_associated #0: 23 / 0.548 -> en:congenital abnormality
    n1=en:microvillus inclusion disease | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=23
  145. en:microvillus inclusion disease -- r_associated #0: 23 / 0.548 -> en:congenital amegakaryocytic thrombocytopenia
    n1=en:microvillus inclusion disease | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=23
  146. en:microvillus inclusion disease -- r_associated #0: 23 / 0.548 -> en:congenital esotropia
    n1=en:microvillus inclusion disease | n2=en:congenital esotropia | rel=r_associated | relid=0 | w=23
  147. en:microvillus inclusion disease -- r_associated #0: 23 / 0.548 -> en:congenital immunodeficiency disease
    n1=en:microvillus inclusion disease | n2=en:congenital immunodeficiency disease | rel=r_associated | relid=0 | w=23
  148. en:microvillus inclusion disease -- r_associated #0: 23 / 0.548 -> en:congenital malformation of upper alimentary tract
    n1=en:microvillus inclusion disease | n2=en:congenital malformation of upper alimentary tract | rel=r_associated | relid=0 | w=23
  149. en:microvillus inclusion disease -- r_associated #0: 23 / 0.548 -> en:congenital monosaccharide malabsorption
    n1=en:microvillus inclusion disease | n2=en:congenital monosaccharide malabsorption | rel=r_associated | relid=0 | w=23
  150. en:microvillus inclusion disease -- r_associated #0: 23 / 0.548 -> en:congenital velopharyngeal dysfunction
    n1=en:microvillus inclusion disease | n2=en:congenital velopharyngeal dysfunction | rel=r_associated | relid=0 | w=23
  151. en:microvillus inclusion disease -- r_associated #0: 23 / 0.548 -> en:disorder of jejunum
    n1=en:microvillus inclusion disease | n2=en:disorder of jejunum | rel=r_associated | relid=0 | w=23
  152. en:microvillus inclusion disease -- r_associated #0: 23 / 0.548 -> en:multiple gastrointestinal atresias (disorder)
    n1=en:microvillus inclusion disease | n2=en:multiple gastrointestinal atresias (disorder) | rel=r_associated | relid=0 | w=23
  153. en:microvillus inclusion disease -- r_associated #0: 23 / 0.548 -> en:other congenital malformations of digestive system
    n1=en:microvillus inclusion disease | n2=en:other congenital malformations of digestive system | rel=r_associated | relid=0 | w=23
  154. en:microvillus inclusion disease -- r_associated #0: 23 / 0.548 -> en:spinal hydromeningocele
    n1=en:microvillus inclusion disease | n2=en:spinal hydromeningocele | rel=r_associated | relid=0 | w=23
  155. en:microvillus inclusion disease -- r_associated #0: 23 / 0.548 -> en:vacterl association
    n1=en:microvillus inclusion disease | n2=en:vacterl association | rel=r_associated | relid=0 | w=23
  156. en:microvillus inclusion disease -- r_associated #0: 22 / 0.524 -> en:congenital anomaly of digestive organ
    n1=en:microvillus inclusion disease | n2=en:congenital anomaly of digestive organ | rel=r_associated | relid=0 | w=22
  157. en:microvillus inclusion disease -- r_associated #0: 22 / 0.524 -> en:congenital auditory imperception
    n1=en:microvillus inclusion disease | n2=en:congenital auditory imperception | rel=r_associated | relid=0 | w=22
  158. en:microvillus inclusion disease -- r_associated #0: 22 / 0.524 -> en:congenital cardiac failure
    n1=en:microvillus inclusion disease | n2=en:congenital cardiac failure | rel=r_associated | relid=0 | w=22
  159. en:microvillus inclusion disease -- r_associated #0: 22 / 0.524 -> en:congenital palato-esophageal incoordination
    n1=en:microvillus inclusion disease | n2=en:congenital palato-esophageal incoordination | rel=r_associated | relid=0 | w=22
  160. en:microvillus inclusion disease -- r_associated #0: 22 / 0.524 -> en:congenital pancreatic cyst
    n1=en:microvillus inclusion disease | n2=en:congenital pancreatic cyst | rel=r_associated | relid=0 | w=22
  161. en:microvillus inclusion disease -- r_associated #0: 22 / 0.524 -> en:congenital pancreatic trypsin deficiency
    n1=en:microvillus inclusion disease | n2=en:congenital pancreatic trypsin deficiency | rel=r_associated | relid=0 | w=22
  162. en:microvillus inclusion disease -- r_associated #0: 22 / 0.524 -> en:congenital stenosis
    n1=en:microvillus inclusion disease | n2=en:congenital stenosis | rel=r_associated | relid=0 | w=22
  163. en:microvillus inclusion disease -- r_associated #0: 22 / 0.524 -> en:dental arch length loss secondary to congenitally missing teeth
    n1=en:microvillus inclusion disease | n2=en:dental arch length loss secondary to congenitally missing teeth | rel=r_associated | relid=0 | w=22
  164. en:microvillus inclusion disease -- r_associated #0: 22 / 0.524 -> en:intestinal disaccharidase deficiency and disaccharide malabsorption
    n1=en:microvillus inclusion disease | n2=en:intestinal disaccharidase deficiency and disaccharide malabsorption | rel=r_associated | relid=0 | w=22
  165. en:microvillus inclusion disease -- r_associated #0: 22 / 0.524 -> en:lymphangiectasia intestinal congenital
    n1=en:microvillus inclusion disease | n2=en:lymphangiectasia intestinal congenital | rel=r_associated | relid=0 | w=22
  166. en:microvillus inclusion disease -- r_associated #0: 22 / 0.524 -> en:pancreatic triacylglycerol lipase deficiency
    n1=en:microvillus inclusion disease | n2=en:pancreatic triacylglycerol lipase deficiency | rel=r_associated | relid=0 | w=22
  167. en:microvillus inclusion disease -- r_associated #0: 22 / 0.524 -> en:rudimentary left ventricle
    n1=en:microvillus inclusion disease | n2=en:rudimentary left ventricle | rel=r_associated | relid=0 | w=22
  168. en:microvillus inclusion disease -- r_associated #0: 21 / 0.5 -> en:anastomotic necrosis of small intestine
    n1=en:microvillus inclusion disease | n2=en:anastomotic necrosis of small intestine | rel=r_associated | relid=0 | w=21
  169. en:microvillus inclusion disease -- r_associated #0: 21 / 0.5 -> en:arthrogryposis
    n1=en:microvillus inclusion disease | n2=en:arthrogryposis | rel=r_associated | relid=0 | w=21
  170. en:microvillus inclusion disease -- r_associated #0: 21 / 0.5 -> en:chronic pseudo-obstruction of small intestine
    n1=en:microvillus inclusion disease | n2=en:chronic pseudo-obstruction of small intestine | rel=r_associated | relid=0 | w=21
  171. en:microvillus inclusion disease -- r_associated #0: 21 / 0.5 -> en:congenital and developmental myasthenia
    n1=en:microvillus inclusion disease | n2=en:congenital and developmental myasthenia | rel=r_associated | relid=0 | w=21
  172. en:microvillus inclusion disease -- r_associated #0: 21 / 0.5 -> en:congenital anomaly of small intestine
    n1=en:microvillus inclusion disease | n2=en:congenital anomaly of small intestine | rel=r_associated | relid=0 | w=21
  173. en:microvillus inclusion disease -- r_associated #0: 21 / 0.5 -> en:congenital anomaly of stomach
    n1=en:microvillus inclusion disease | n2=en:congenital anomaly of stomach | rel=r_associated | relid=0 | w=21
  174. en:microvillus inclusion disease -- r_associated #0: 21 / 0.5 -> en:congenital hearing disorder
    n1=en:microvillus inclusion disease | n2=en:congenital hearing disorder | rel=r_associated | relid=0 | w=21
  175. en:microvillus inclusion disease -- r_associated #0: 21 / 0.5 -> en:congenital melanocytic nevus of trunk
    n1=en:microvillus inclusion disease | n2=en:congenital melanocytic nevus of trunk | rel=r_associated | relid=0 | w=21
  176. en:microvillus inclusion disease -- r_associated #0: 21 / 0.5 -> en:diaphragm disease of intestine
    n1=en:microvillus inclusion disease | n2=en:diaphragm disease of intestine | rel=r_associated | relid=0 | w=21
  177. en:microvillus inclusion disease -- r_associated #0: 21 / 0.5 -> en:diphyllobothrium latum infection
    n1=en:microvillus inclusion disease | n2=en:diphyllobothrium latum infection | rel=r_associated | relid=0 | w=21
  178. en:microvillus inclusion disease -- r_associated #0: 21 / 0.5 -> en:gastrointestinal vessel anomaly
    n1=en:microvillus inclusion disease | n2=en:gastrointestinal vessel anomaly | rel=r_associated | relid=0 | w=21
  179. en:microvillus inclusion disease -- r_associated #0: 21 / 0.5 -> en:infant metachromatic leukodystrophies
    n1=en:microvillus inclusion disease | n2=en:infant metachromatic leukodystrophies | rel=r_associated | relid=0 | w=21
  180. en:microvillus inclusion disease -- r_associated #0: 21 / 0.5 -> en:pseudomonas pyocyaneus congenital infection
    n1=en:microvillus inclusion disease | n2=en:pseudomonas pyocyaneus congenital infection | rel=r_associated | relid=0 | w=21
  181. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> acrodermatite entéropathique
    n1=en:microvillus inclusion disease | n2=acrodermatite entéropathique | rel=r_associated | relid=0 | w=20
  182. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> affection oculaire congénitale
    n1=en:microvillus inclusion disease | n2=affection oculaire congénitale | rel=r_associated | relid=0 | w=20
  183. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> anomalie chromosomique
    n1=en:microvillus inclusion disease | n2=anomalie chromosomique | rel=r_associated | relid=0 | w=20
  184. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> anomalie congénitale de l'oeil
    n1=en:microvillus inclusion disease | n2=anomalie congénitale de l'oeil | rel=r_associated | relid=0 | w=20
  185. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> anomalie cytogénétique
    n1=en:microvillus inclusion disease | n2=anomalie cytogénétique | rel=r_associated | relid=0 | w=20
  186. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> anomalie du développement
    n1=en:microvillus inclusion disease | n2=anomalie du développement | rel=r_associated | relid=0 | w=20
  187. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> anomalies buccales
    n1=en:microvillus inclusion disease | n2=anomalies buccales | rel=r_associated | relid=0 | w=20
  188. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> anomalies de la bouche
    n1=en:microvillus inclusion disease | n2=anomalies de la bouche | rel=r_associated | relid=0 | w=20
  189. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> anormalité des chromosomes
    n1=en:microvillus inclusion disease | n2=anormalité des chromosomes | rel=r_associated | relid=0 | w=20
  190. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> anus contre nature
    n1=en:microvillus inclusion disease | n2=anus contre nature | rel=r_associated | relid=0 | w=20
  191. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> anus praeter
    n1=en:microvillus inclusion disease | n2=anus praeter | rel=r_associated | relid=0 | w=20
  192. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> arthrogrypose
    n1=en:microvillus inclusion disease | n2=arthrogrypose | rel=r_associated | relid=0 | w=20
  193. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> congénital
    n1=en:microvillus inclusion disease | n2=congénital | rel=r_associated | relid=0 | w=20
  194. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> congenital
    n1=en:microvillus inclusion disease | n2=congenital | rel=r_associated | relid=0 | w=20
  195. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> congénitale
    n1=en:microvillus inclusion disease | n2=congénitale | rel=r_associated | relid=0 | w=20
  196. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> contractures congénitales et arachnodactylie
    n1=en:microvillus inclusion disease | n2=contractures congénitales et arachnodactylie | rel=r_associated | relid=0 | w=20
  197. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> créatorrhée
    n1=en:microvillus inclusion disease | n2=créatorrhée | rel=r_associated | relid=0 | w=20
  198. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> débilité congénitale du foetus
    n1=en:microvillus inclusion disease | n2=débilité congénitale du foetus | rel=r_associated | relid=0 | w=20
  199. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> débilité congénitale foetale
    n1=en:microvillus inclusion disease | n2=débilité congénitale foetale | rel=r_associated | relid=0 | w=20
  200. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> déficience congénitale
    n1=en:microvillus inclusion disease | n2=déficience congénitale | rel=r_associated | relid=0 | w=20
  201. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> déformation congénitale
    n1=en:microvillus inclusion disease | n2=déformation congénitale | rel=r_associated | relid=0 | w=20
  202. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> difformité congénitale
    n1=en:microvillus inclusion disease | n2=difformité congénitale | rel=r_associated | relid=0 | w=20
  203. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> diverticule de meckel
    n1=en:microvillus inclusion disease | n2=diverticule de meckel | rel=r_associated | relid=0 | w=20
  204. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> Diverticule de Meckel
    n1=en:microvillus inclusion disease | n2=Diverticule de Meckel | rel=r_associated | relid=0 | w=20
  205. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> diverticule de Meckel
    n1=en:microvillus inclusion disease | n2=diverticule de Meckel | rel=r_associated | relid=0 | w=20
  206. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:acquired fructose intolerance
    n1=en:microvillus inclusion disease | n2=en:acquired fructose intolerance | rel=r_associated | relid=0 | w=20
  207. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:acquired lactase deficiency
    n1=en:microvillus inclusion disease | n2=en:acquired lactase deficiency | rel=r_associated | relid=0 | w=20
  208. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:adenomatosis coli
    n1=en:microvillus inclusion disease | n2=en:adenomatosis coli | rel=r_associated | relid=0 | w=20
  209. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:amyloidosis of small intestine
    n1=en:microvillus inclusion disease | n2=en:amyloidosis of small intestine | rel=r_associated | relid=0 | w=20
  210. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:anal imperforation
    n1=en:microvillus inclusion disease | n2=en:anal imperforation | rel=r_associated | relid=0 | w=20
  211. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:anterior displaced anus
    n1=en:microvillus inclusion disease | n2=en:anterior displaced anus | rel=r_associated | relid=0 | w=20
  212. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:bile acid malabsorption
    n1=en:microvillus inclusion disease | n2=en:bile acid malabsorption | rel=r_associated | relid=0 | w=20
  213. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:bile acid malabsorption syndrome
    n1=en:microvillus inclusion disease | n2=en:bile acid malabsorption syndrome | rel=r_associated | relid=0 | w=20
  214. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:birth defect
    n1=en:microvillus inclusion disease | n2=en:birth defect | rel=r_associated | relid=0 | w=20
  215. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:carbohydrate intolerance
    n1=en:microvillus inclusion disease | n2=en:carbohydrate intolerance | rel=r_associated | relid=0 | w=20
  216. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:chemically-induced malabsorption
    n1=en:microvillus inclusion disease | n2=en:chemically-induced malabsorption | rel=r_associated | relid=0 | w=20
  217. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:childhood celiac disease
    n1=en:microvillus inclusion disease | n2=en:childhood celiac disease | rel=r_associated | relid=0 | w=20
  218. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:choledochal cyst
    n1=en:microvillus inclusion disease | n2=en:choledochal cyst | rel=r_associated | relid=0 | w=20
  219. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:chromosomal aberration
    n1=en:microvillus inclusion disease | n2=en:chromosomal aberration | rel=r_associated | relid=0 | w=20
  220. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:chromosomal abnormality
    n1=en:microvillus inclusion disease | n2=en:chromosomal abnormality | rel=r_associated | relid=0 | w=20
  221. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:coeliac disease
    n1=en:microvillus inclusion disease | n2=en:coeliac disease | rel=r_associated | relid=0 | w=20
  222. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:coeliac sprue
    n1=en:microvillus inclusion disease | n2=en:coeliac sprue | rel=r_associated | relid=0 | w=20
  223. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:congenital analbuminemia
    n1=en:microvillus inclusion disease | n2=en:congenital analbuminemia | rel=r_associated | relid=0 | w=20
  224. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:congenital anomaly
    n1=en:microvillus inclusion disease | n2=en:congenital anomaly | rel=r_associated | relid=0 | w=20
  225. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:congenital chloride diarrhea
    n1=en:microvillus inclusion disease | n2=en:congenital chloride diarrhea | rel=r_associated | relid=0 | w=20
  226. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:congenital complete atrioventricular block
    n1=en:microvillus inclusion disease | n2=en:congenital complete atrioventricular block | rel=r_associated | relid=0 | w=20
  227. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:congenital cyst of aryepiglottic fold
    n1=en:microvillus inclusion disease | n2=en:congenital cyst of aryepiglottic fold | rel=r_associated | relid=0 | w=20
  228. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:congenital defect
    n1=en:microvillus inclusion disease | n2=en:congenital defect | rel=r_associated | relid=0 | w=20
  229. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:congenital digestive system disorder
    n1=en:microvillus inclusion disease | n2=en:congenital digestive system disorder | rel=r_associated | relid=0 | w=20
  230. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:congenital kyphosis
    n1=en:microvillus inclusion disease | n2=en:congenital kyphosis | rel=r_associated | relid=0 | w=20
  231. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:congenital laryngeal cyst
    n1=en:microvillus inclusion disease | n2=en:congenital laryngeal cyst | rel=r_associated | relid=0 | w=20
  232. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:congenital malformation
    n1=en:microvillus inclusion disease | n2=en:congenital malformation | rel=r_associated | relid=0 | w=20
  233. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:congenital megaprepuce
    n1=en:microvillus inclusion disease | n2=en:congenital megaprepuce | rel=r_associated | relid=0 | w=20
  234. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:congenital metabolic disorder
    n1=en:microvillus inclusion disease | n2=en:congenital metabolic disorder | rel=r_associated | relid=0 | w=20
  235. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:congenital pain insensitivity
    n1=en:microvillus inclusion disease | n2=en:congenital pain insensitivity | rel=r_associated | relid=0 | w=20
  236. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:congenital quadriplegia
    n1=en:microvillus inclusion disease | n2=en:congenital quadriplegia | rel=r_associated | relid=0 | w=20
  237. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:creatorrhoea
    n1=en:microvillus inclusion disease | n2=en:creatorrhoea | rel=r_associated | relid=0 | w=20
  238. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:developmental anomaly
    n1=en:microvillus inclusion disease | n2=en:developmental anomaly | rel=r_associated | relid=0 | w=20
  239. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:developmental fault
    n1=en:microvillus inclusion disease | n2=en:developmental fault | rel=r_associated | relid=0 | w=20
  240. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:diverticulosis of small intestine
    n1=en:microvillus inclusion disease | n2=en:diverticulosis of small intestine | rel=r_associated | relid=0 | w=20
  241. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:duodenal diseases
    n1=en:microvillus inclusion disease | n2=en:duodenal diseases | rel=r_associated | relid=0 | w=20
  242. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:enteritis
    n1=en:microvillus inclusion disease | n2=en:enteritis | rel=r_associated | relid=0 | w=20
  243. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:enteronitis
    n1=en:microvillus inclusion disease | n2=en:enteronitis | rel=r_associated | relid=0 | w=20
  244. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:enterostomy malfunction
    n1=en:microvillus inclusion disease | n2=en:enterostomy malfunction | rel=r_associated | relid=0 | w=20
  245. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:erythropoietic porphyria
    n1=en:microvillus inclusion disease | n2=en:erythropoietic porphyria | rel=r_associated | relid=0 | w=20
  246. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:foreign body in small intestine
    n1=en:microvillus inclusion disease | n2=en:foreign body in small intestine | rel=r_associated | relid=0 | w=20
  247. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:gastrointestinal malabsorption syndrome co-occurrent with human immunodeficiency virus infection
    n1=en:microvillus inclusion disease | n2=en:gastrointestinal malabsorption syndrome co-occurrent with human immunodeficiency virus infection | rel=r_associated | relid=0 | w=20
  248. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:gluten induced enteropathy
    n1=en:microvillus inclusion disease | n2=en:gluten induced enteropathy | rel=r_associated | relid=0 | w=20
  249. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:hamartoma of small intestine
    n1=en:microvillus inclusion disease | n2=en:hamartoma of small intestine | rel=r_associated | relid=0 | w=20
  250. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:hereditary non-polyposis colorectal cancer syndrome
    n1=en:microvillus inclusion disease | n2=en:hereditary non-polyposis colorectal cancer syndrome | rel=r_associated | relid=0 | w=20
  251. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:hill diarrhea
    n1=en:microvillus inclusion disease | n2=en:hill diarrhea | rel=r_associated | relid=0 | w=20
  252. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:hyperhomocysteinemia
    n1=en:microvillus inclusion disease | n2=en:hyperhomocysteinemia | rel=r_associated | relid=0 | w=20
  253. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:hypopituitarism
    n1=en:microvillus inclusion disease | n2=en:hypopituitarism | rel=r_associated | relid=0 | w=20
  254. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:infantile myofibromatosis
    n1=en:microvillus inclusion disease | n2=en:infantile myofibromatosis | rel=r_associated | relid=0 | w=20
  255. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:intestinal pseudo-obstruction
    n1=en:microvillus inclusion disease | n2=en:intestinal pseudo-obstruction | rel=r_associated | relid=0 | w=20
  256. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:lactose intolerance, adult type
    n1=en:microvillus inclusion disease | n2=en:lactose intolerance, adult type | rel=r_associated | relid=0 | w=20
  257. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:major physical defect
    n1=en:microvillus inclusion disease | n2=en:major physical defect | rel=r_associated | relid=0 | w=20
  258. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:malabsorption
    n1=en:microvillus inclusion disease | n2=en:malabsorption | rel=r_associated | relid=0 | w=20
  259. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:malabsorption syndrome
    n1=en:microvillus inclusion disease | n2=en:malabsorption syndrome | rel=r_associated | relid=0 | w=20
  260. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:meckel diverticulum
    n1=en:microvillus inclusion disease | n2=en:meckel diverticulum | rel=r_associated | relid=0 | w=20
  261. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:megaloblastic anemia due to disease of small intestine
    n1=en:microvillus inclusion disease | n2=en:megaloblastic anemia due to disease of small intestine | rel=r_associated | relid=0 | w=20
  262. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:megophthalmos
    n1=en:microvillus inclusion disease | n2=en:megophthalmos | rel=r_associated | relid=0 | w=20
  263. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:microvillus alteration
    n1=en:microvillus inclusion disease | n2=en:microvillus alteration | rel=r_associated | relid=0 | w=20
  264. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:mottled teeth, congenital
    n1=en:microvillus inclusion disease | n2=en:mottled teeth, congenital | rel=r_associated | relid=0 | w=20
  265. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:mucolipidosis
    n1=en:microvillus inclusion disease | n2=en:mucolipidosis | rel=r_associated | relid=0 | w=20
  266. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:muir-torre syndrome
    n1=en:microvillus inclusion disease | n2=en:muir-torre syndrome | rel=r_associated | relid=0 | w=20
  267. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:non tropical sprue
    n1=en:microvillus inclusion disease | n2=en:non tropical sprue | rel=r_associated | relid=0 | w=20
  268. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:nystagmus
    n1=en:microvillus inclusion disease | n2=en:nystagmus | rel=r_associated | relid=0 | w=20
  269. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:palmoplantar porokeratosis
    n1=en:microvillus inclusion disease | n2=en:palmoplantar porokeratosis | rel=r_associated | relid=0 | w=20
  270. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:patent foramen ovale
    n1=en:microvillus inclusion disease | n2=en:patent foramen ovale | rel=r_associated | relid=0 | w=20
  271. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:physical defect
    n1=en:microvillus inclusion disease | n2=en:physical defect | rel=r_associated | relid=0 | w=20
  272. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:pigmented paravenous chorioretinal atrophy
    n1=en:microvillus inclusion disease | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20
  273. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:postcholecystectomy diarrhea
    n1=en:microvillus inclusion disease | n2=en:postcholecystectomy diarrhea | rel=r_associated | relid=0 | w=20
  274. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:Prader-Willi syndrome
    n1=en:microvillus inclusion disease | n2=en:Prader-Willi syndrome | rel=r_associated | relid=0 | w=20
  275. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:pretematural anus
    n1=en:microvillus inclusion disease | n2=en:pretematural anus | rel=r_associated | relid=0 | w=20
  276. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:small bowel inflammation
    n1=en:microvillus inclusion disease | n2=en:small bowel inflammation | rel=r_associated | relid=0 | w=20
  277. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:small intestinal gangrene
    n1=en:microvillus inclusion disease | n2=en:small intestinal gangrene | rel=r_associated | relid=0 | w=20
  278. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:small intestinal obstruction
    n1=en:microvillus inclusion disease | n2=en:small intestinal obstruction | rel=r_associated | relid=0 | w=20
  279. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:small intestinal stasis syndrome
    n1=en:microvillus inclusion disease | n2=en:small intestinal stasis syndrome | rel=r_associated | relid=0 | w=20
  280. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:small intestinal ulcer
    n1=en:microvillus inclusion disease | n2=en:small intestinal ulcer | rel=r_associated | relid=0 | w=20
  281. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:sprue
    n1=en:microvillus inclusion disease | n2=en:sprue | rel=r_associated | relid=0 | w=20
  282. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:teratosis
    n1=en:microvillus inclusion disease | n2=en:teratosis | rel=r_associated | relid=0 | w=20
  283. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:tooth malformation
    n1=en:microvillus inclusion disease | n2=en:tooth malformation | rel=r_associated | relid=0 | w=20
  284. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:toxemic infantilism
    n1=en:microvillus inclusion disease | n2=en:toxemic infantilism | rel=r_associated | relid=0 | w=20
  285. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:villous atrophy of intestine
    n1=en:microvillus inclusion disease | n2=en:villous atrophy of intestine | rel=r_associated | relid=0 | w=20
  286. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:whipple disease
    n1=en:microvillus inclusion disease | n2=en:whipple disease | rel=r_associated | relid=0 | w=20
  287. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:Whipple disease
    n1=en:microvillus inclusion disease | n2=en:Whipple disease | rel=r_associated | relid=0 | w=20
  288. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:Williams syndrome
    n1=en:microvillus inclusion disease | n2=en:Williams syndrome | rel=r_associated | relid=0 | w=20
  289. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:williams syndrome
    n1=en:microvillus inclusion disease | n2=en:williams syndrome | rel=r_associated | relid=0 | w=20
  290. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> en:zinc-deficiency type
    n1=en:microvillus inclusion disease | n2=en:zinc-deficiency type | rel=r_associated | relid=0 | w=20
  291. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> entérite
    n1=en:microvillus inclusion disease | n2=entérite | rel=r_associated | relid=0 | w=20
  292. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> entérospasme
    n1=en:microvillus inclusion disease | n2=entérospasme | rel=r_associated | relid=0 | w=20
  293. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> foramen ovale perméable
    n1=en:microvillus inclusion disease | n2=foramen ovale perméable | rel=r_associated | relid=0 | w=20
  294. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> gluten (intolérance au)
    n1=en:microvillus inclusion disease | n2=gluten (intolérance au) | rel=r_associated | relid=0 | w=20
  295. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale
    n1=en:microvillus inclusion disease | n2=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | rel=r_associated | relid=0 | w=20
  296. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> imperforation anale
    n1=en:microvillus inclusion disease | n2=imperforation anale | rel=r_associated | relid=0 | w=20
  297. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> imperforation de l'anus
    n1=en:microvillus inclusion disease | n2=imperforation de l'anus | rel=r_associated | relid=0 | w=20
  298. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> intestin irritable (syndrome de l')
    n1=en:microvillus inclusion disease | n2=intestin irritable (syndrome de l') | rel=r_associated | relid=0 | w=20
  299. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> intolérance au fructose
    n1=en:microvillus inclusion disease | n2=intolérance au fructose | rel=r_associated | relid=0 | w=20
  300. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> intolérance au lactose
    n1=en:microvillus inclusion disease | n2=intolérance au lactose | rel=r_associated | relid=0 | w=20
  301. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> Intolérance au lactose
    n1=en:microvillus inclusion disease | n2=Intolérance au lactose | rel=r_associated | relid=0 | w=20
  302. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> intolérance au saccharose
    n1=en:microvillus inclusion disease | n2=intolérance au saccharose | rel=r_associated | relid=0 | w=20
  303. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> malabsorption
    n1=en:microvillus inclusion disease | n2=malabsorption | rel=r_associated | relid=0 | w=20
  304. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> maladie c?liaque
    n1=en:microvillus inclusion disease | n2=maladie c?liaque | rel=r_associated | relid=0 | w=20
  305. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> maladie coeliaque
    n1=en:microvillus inclusion disease | n2=maladie coeliaque | rel=r_associated | relid=0 | w=20
  306. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> maladie coeliaque de l'enfant
    n1=en:microvillus inclusion disease | n2=maladie coeliaque de l'enfant | rel=r_associated | relid=0 | w=20
  307. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> maladie congénitale
    n1=en:microvillus inclusion disease | n2=maladie congénitale | rel=r_associated | relid=0 | w=20
  308. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> maladie de Whipple
    n1=en:microvillus inclusion disease | n2=maladie de Whipple | rel=r_associated | relid=0 | w=20
  309. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> maladie de whipple
    n1=en:microvillus inclusion disease | n2=maladie de whipple | rel=r_associated | relid=0 | w=20
  310. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> Maladie de Whipple
    n1=en:microvillus inclusion disease | n2=Maladie de Whipple | rel=r_associated | relid=0 | w=20
  311. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> malformation
    n1=en:microvillus inclusion disease | n2=malformation | rel=r_associated | relid=0 | w=20
  312. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> malformation congénitale
    n1=en:microvillus inclusion disease | n2=malformation congénitale | rel=r_associated | relid=0 | w=20
  313. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> malformations buccales
    n1=en:microvillus inclusion disease | n2=malformations buccales | rel=r_associated | relid=0 | w=20
  314. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> malformations de la bouche
    n1=en:microvillus inclusion disease | n2=malformations de la bouche | rel=r_associated | relid=0 | w=20
  315. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> méthémoglobinémie congénitale
    n1=en:microvillus inclusion disease | n2=méthémoglobinémie congénitale | rel=r_associated | relid=0 | w=20
  316. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> microvillus
    n1=en:microvillus inclusion disease | n2=microvillus | rel=r_associated | relid=0 | w=20
  317. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> mucolipidose
    n1=en:microvillus inclusion disease | n2=mucolipidose | rel=r_associated | relid=0 | w=20
  318. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> myofibromatose infantile
    n1=en:microvillus inclusion disease | n2=myofibromatose infantile | rel=r_associated | relid=0 | w=20
  319. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> nystagmus congénital isolé
    n1=en:microvillus inclusion disease | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
  320. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> pathologie congénitale
    n1=en:microvillus inclusion disease | n2=pathologie congénitale | rel=r_associated | relid=0 | w=20
  321. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> persistance du foramen ovale
    n1=en:microvillus inclusion disease | n2=persistance du foramen ovale | rel=r_associated | relid=0 | w=20
  322. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> polyadénomatose recto-colique familiale
    n1=en:microvillus inclusion disease | n2=polyadénomatose recto-colique familiale | rel=r_associated | relid=0 | w=20
  323. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> polypose adénomateuse familiale
    n1=en:microvillus inclusion disease | n2=polypose adénomateuse familiale | rel=r_associated | relid=0 | w=20
  324. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> polypose colique familiale
    n1=en:microvillus inclusion disease | n2=polypose colique familiale | rel=r_associated | relid=0 | w=20
  325. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> polypose recto-colique familiale
    n1=en:microvillus inclusion disease | n2=polypose recto-colique familiale | rel=r_associated | relid=0 | w=20
  326. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> polypose rectocolique
    n1=en:microvillus inclusion disease | n2=polypose rectocolique | rel=r_associated | relid=0 | w=20
  327. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> polypose rectocolique familiale
    n1=en:microvillus inclusion disease | n2=polypose rectocolique familiale | rel=r_associated | relid=0 | w=20
  328. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> porphyrie érythropoïétique
    n1=en:microvillus inclusion disease | n2=porphyrie érythropoïétique | rel=r_associated | relid=0 | w=20
  329. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> rétinite pigmentaire paraveineuse
    n1=en:microvillus inclusion disease | n2=rétinite pigmentaire paraveineuse | rel=r_associated | relid=0 | w=20
  330. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> sprue
    n1=en:microvillus inclusion disease | n2=sprue | rel=r_associated | relid=0 | w=20
  331. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> sprue tropicale
    n1=en:microvillus inclusion disease | n2=sprue tropicale | rel=r_associated | relid=0 | w=20
  332. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> stéatorrhée tropicale
    n1=en:microvillus inclusion disease | n2=stéatorrhée tropicale | rel=r_associated | relid=0 | w=20
  333. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> syndrome de malabsorption
    n1=en:microvillus inclusion disease | n2=syndrome de malabsorption | rel=r_associated | relid=0 | w=20
  334. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> syndrome de Williams
    n1=en:microvillus inclusion disease | n2=syndrome de Williams | rel=r_associated | relid=0 | w=20
  335. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> syndrome du grêle court
    n1=en:microvillus inclusion disease | n2=syndrome du grêle court | rel=r_associated | relid=0 | w=20
  336. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> tare congénitale
    n1=en:microvillus inclusion disease | n2=tare congénitale | rel=r_associated | relid=0 | w=20
  337. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> trouble chromosomique
    n1=en:microvillus inclusion disease | n2=trouble chromosomique | rel=r_associated | relid=0 | w=20
  338. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> vestige du conduit vitellin
    n1=en:microvillus inclusion disease | n2=vestige du conduit vitellin | rel=r_associated | relid=0 | w=20
  339. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> vice de conformation
    n1=en:microvillus inclusion disease | n2=vice de conformation | rel=r_associated | relid=0 | w=20
  340. en:microvillus inclusion disease -- r_associated #0: 20 / 0.476 -> Whipple (maladie de)
    n1=en:microvillus inclusion disease | n2=Whipple (maladie de) | rel=r_associated | relid=0 | w=20
≈ 468 relations entrantes

  1. anomalie congénitale --- r_associated #0: 424 --> en:microvillus inclusion disease
    n1=anomalie congénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=424
  2. en:congenital abnormality --- r_associated #0: 421 --> en:microvillus inclusion disease
    n1=en:congenital abnormality | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=421
  3. malformation congénitale --- r_associated #0: 356 --> en:microvillus inclusion disease
    n1=malformation congénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=356
  4. en:congenital anomaly --- r_associated #0: 352 --> en:microvillus inclusion disease
    n1=en:congenital anomaly | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=352
  5. anormalité des chromosomes --- r_associated #0: 322 --> en:microvillus inclusion disease
    n1=anormalité des chromosomes | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=322
  6. en:chromosome disorder --- r_associated #0: 320 --> en:microvillus inclusion disease
    n1=en:chromosome disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=320
  7. en:congenital defect --- r_associated #0: 310 --> en:microvillus inclusion disease
    n1=en:congenital defect | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=310
  8. déformation congénitale --- r_associated #0: 286 --> en:microvillus inclusion disease
    n1=déformation congénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=286
  9. déficience congénitale --- r_associated #0: 275 --> en:microvillus inclusion disease
    n1=déficience congénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=275
  10. trouble chromosomique --- r_associated #0: 250 --> en:microvillus inclusion disease
    n1=trouble chromosomique | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=250
  11. anomalie chromosomique --- r_associated #0: 249 --> en:microvillus inclusion disease
    n1=anomalie chromosomique | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=249
  12. anomalie congénitale de l'oeil --- r_associated #0: 208 --> en:microvillus inclusion disease
    n1=anomalie congénitale de l'oeil | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=208
  13. en:congenital eye disorder --- r_associated #0: 205 --> en:microvillus inclusion disease
    n1=en:congenital eye disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=205
  14. maladie congénitale --- r_associated #0: 202 --> en:microvillus inclusion disease
    n1=maladie congénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=202
  15. difformité congénitale --- r_associated #0: 195 --> en:microvillus inclusion disease
    n1=difformité congénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=195
  16. pathologie congénitale --- r_associated #0: 195 --> en:microvillus inclusion disease
    n1=pathologie congénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=195
  17. affection oculaire congénitale --- r_associated #0: 180 --> en:microvillus inclusion disease
    n1=affection oculaire congénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=180
  18. en:chromosomal abnormality --- r_associated #0: 180 --> en:microvillus inclusion disease
    n1=en:chromosomal abnormality | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=180
  19. en:arthrogryposis --- r_associated #0: 159 --> en:microvillus inclusion disease
    n1=en:arthrogryposis | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=159
  20. arthrogrypose --- r_associated #0: 155 --> en:microvillus inclusion disease
    n1=arthrogrypose | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=155
  21. débilité congénitale du foetus --- r_associated #0: 135 --> en:microvillus inclusion disease
    n1=débilité congénitale du foetus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=135
  22. en:congenital debility of fetus --- r_associated #0: 134 --> en:microvillus inclusion disease
    n1=en:congenital debility of fetus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=134
  23. en:whipple disease --- r_associated #0: 131 --> en:microvillus inclusion disease
    n1=en:whipple disease | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=131
  24. en:congenital malformation --- r_associated #0: 130 --> en:microvillus inclusion disease
    n1=en:congenital malformation | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=130
  25. maladie de Whipple --- r_associated #0: 130 --> en:microvillus inclusion disease
    n1=maladie de Whipple | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=130
  26. en:congenital methemoglobinemia --- r_associated #0: 123 --> en:microvillus inclusion disease
    n1=en:congenital methemoglobinemia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=123
  27. anus praeter --- r_associated #0: 120 --> en:microvillus inclusion disease
    n1=anus praeter | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=120
  28. en:birth defect --- r_associated #0: 120 --> en:microvillus inclusion disease
    n1=en:birth defect | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=120
  29. méthémoglobinémie congénitale --- r_associated #0: 120 --> en:microvillus inclusion disease
    n1=méthémoglobinémie congénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=120
  30. en:preternatural anus --- r_associated #0: 116 --> en:microvillus inclusion disease
    n1=en:preternatural anus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=116
  31. anus contre nature --- r_associated #0: 111 --> en:microvillus inclusion disease
    n1=anus contre nature | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=111
  32. débilité congénitale foetale --- r_associated #0: 110 --> en:microvillus inclusion disease
    n1=débilité congénitale foetale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=110
  33. atrésie de l'oesophage --- r_associated #0: 96 --> en:microvillus inclusion disease
    n1=atrésie de l'oesophage | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=96
  34. atrésie de l'œsophage --- r_associated #0: 96 --> en:microvillus inclusion disease
    n1=atrésie de l'œsophage | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=96
  35. atrésie de l'œsophage --- r_associated #0: 95 --> en:microvillus inclusion disease
    n1=atrésie de l'œsophage | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=95
  36. tare congénitale --- r_associated #0: 85 --> en:microvillus inclusion disease
    n1=tare congénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=85
  37. malformations de la bouche --- r_associated #0: 80 --> en:microvillus inclusion disease
    n1=malformations de la bouche | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=80
  38. sprue --- r_associated #0: 80 --> en:microvillus inclusion disease
    n1=sprue | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=80
  39. en:sprue --- r_associated #0: 79 --> en:microvillus inclusion disease
    n1=en:sprue | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=79
  40. anomalies de la bouche --- r_associated #0: 76 --> en:microvillus inclusion disease
    n1=anomalies de la bouche | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=76
  41. en:microvillus --- r_associated #0: 75 --> en:microvillus inclusion disease
    n1=en:microvillus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=75
  42. anomalies buccales --- r_associated #0: 73 --> en:microvillus inclusion disease
    n1=anomalies buccales | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=73
  43. en:Whipple disease --- r_associated #0: 73 --> en:microvillus inclusion disease
    n1=en:Whipple disease | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=73
  44. en:mouth abnormalities --- r_associated #0: 72 --> en:microvillus inclusion disease
    n1=en:mouth abnormalities | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=72
  45. microvillus --- r_associated #0: 71 --> en:microvillus inclusion disease
    n1=microvillus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=71
  46. malformations buccales --- r_associated #0: 64 --> en:microvillus inclusion disease
    n1=malformations buccales | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=64
  47. persistance du foramen ovale --- r_associated #0: 61 --> en:microvillus inclusion disease
    n1=persistance du foramen ovale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=61
  48. anomalie cytogénétique --- r_associated #0: 60 --> en:microvillus inclusion disease
    n1=anomalie cytogénétique | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=60
  49. en:pretematural anus --- r_associated #0: 60 --> en:microvillus inclusion disease
    n1=en:pretematural anus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=60
  50. stéatorrhée tropicale --- r_associated #0: 60 --> en:microvillus inclusion disease
    n1=stéatorrhée tropicale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=60
  51. congénitale --- r_associated #0: 59 --> en:microvillus inclusion disease
    n1=congénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=59
  52. en:congenital --- r_associated #0: 59 --> en:microvillus inclusion disease
    n1=en:congenital | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=59
  53. vice de conformation --- r_associated #0: 59 --> en:microvillus inclusion disease
    n1=vice de conformation | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=59
  54. congenital --- r_associated #0: 57 --> en:microvillus inclusion disease
    n1=congenital | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=57
  55. en:patent foramen ovale --- r_associated #0: 57 --> en:microvillus inclusion disease
    n1=en:patent foramen ovale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=57
  56. sprue tropicale --- r_associated #0: 57 --> en:microvillus inclusion disease
    n1=sprue tropicale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=57
  57. en:tropical sprue --- r_associated #0: 55 --> en:microvillus inclusion disease
    n1=en:tropical sprue | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=55
  58. entérite --- r_associated #0: 55 --> en:microvillus inclusion disease
    n1=entérite | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=55
  59. malabsorption --- r_associated #0: 55 --> en:microvillus inclusion disease
    n1=malabsorption | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=55
  60. vestige du conduit vitellin --- r_associated #0: 55 --> en:microvillus inclusion disease
    n1=vestige du conduit vitellin | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=55
  61. congénital --- r_associated #0: 54 --> en:microvillus inclusion disease
    n1=congénital | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=54
  62. en:enteritis --- r_associated #0: 54 --> en:microvillus inclusion disease
    n1=en:enteritis | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=54
  63. en:malabsorption --- r_associated #0: 54 --> en:microvillus inclusion disease
    n1=en:malabsorption | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=54
  64. en:meckel diverticulum --- r_associated #0: 53 --> en:microvillus inclusion disease
    n1=en:meckel diverticulum | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=53
  65. acrodermatite entéropathique --- r_associated #0: 50 --> en:microvillus inclusion disease
    n1=acrodermatite entéropathique | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=50
  66. maladie cœliaque --- r_associated #0: 50 --> en:microvillus inclusion disease
    n1=maladie cœliaque | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=50
  67. polypose colique familiale --- r_associated #0: 50 --> en:microvillus inclusion disease
    n1=polypose colique familiale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=50
  68. en:prader-willi syndrome --- r_associated #0: 49 --> en:microvillus inclusion disease
    n1=en:prader-willi syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=49
  69. foramen ovale perméable --- r_associated #0: 49 --> en:microvillus inclusion disease
    n1=foramen ovale perméable | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=49
  70. anomalie du développement --- r_associated #0: 48 --> en:microvillus inclusion disease
    n1=anomalie du développement | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=48
  71. en:acrodermatitis enteropathica --- r_associated #0: 48 --> en:microvillus inclusion disease
    n1=en:acrodermatitis enteropathica | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=48
  72. en:non tropical sprue --- r_associated #0: 48 --> en:microvillus inclusion disease
    n1=en:non tropical sprue | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=48
  73. maladie coeliaque --- r_associated #0: 48 --> en:microvillus inclusion disease
    n1=maladie coeliaque | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=48
  74. en:familial adenomatous polyposis --- r_associated #0: 47 --> en:microvillus inclusion disease
    n1=en:familial adenomatous polyposis | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=47
  75. en:major physical defect --- r_associated #0: 47 --> en:microvillus inclusion disease
    n1=en:major physical defect | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=47
  76. en:physical defect --- r_associated #0: 47 --> en:microvillus inclusion disease
    n1=en:physical defect | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=47
  77. en:gluten induced enteropathy --- r_associated #0: 46 --> en:microvillus inclusion disease
    n1=en:gluten induced enteropathy | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=46
  78. en:small bowel inflammation --- r_associated #0: 46 --> en:microvillus inclusion disease
    n1=en:small bowel inflammation | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=46
  79. diverticule de Meckel --- r_associated #0: 45 --> en:microvillus inclusion disease
    n1=diverticule de Meckel | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=45
  80. en:Prader-Willi syndrome --- r_associated #0: 45 --> en:microvillus inclusion disease
    n1=en:Prader-Willi syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=45
  81. intolérance au fructose --- r_associated #0: 45 --> en:microvillus inclusion disease
    n1=intolérance au fructose | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=45
  82. Intolérance au lactose --- r_associated #0: 44 --> en:microvillus inclusion disease
    n1=Intolérance au lactose | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=44
  83. en:coeliac sprue --- r_associated #0: 44 --> en:microvillus inclusion disease
    n1=en:coeliac sprue | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=44
  84. en:teratosis --- r_associated #0: 44 --> en:microvillus inclusion disease
    n1=en:teratosis | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=44
  85. syndrome du grêle court --- r_associated #0: 44 --> en:microvillus inclusion disease
    n1=syndrome du grêle court | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=44
  86. en:congenital hydrocele --- r_associated #0: 43 --> en:microvillus inclusion disease
    n1=en:congenital hydrocele | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=43
  87. en:creatorrhoea --- r_associated #0: 43 --> en:microvillus inclusion disease
    n1=en:creatorrhoea | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=43
  88. en:hereditary fructose intolerance --- r_associated #0: 43 --> en:microvillus inclusion disease
    n1=en:hereditary fructose intolerance | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=43
  89. en:infection by diphyllobothrium pacificum --- r_associated #0: 43 --> en:microvillus inclusion disease
    n1=en:infection by diphyllobothrium pacificum | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=43
  90. en:short bowel syndrome --- r_associated #0: 43 --> en:microvillus inclusion disease
    n1=en:short bowel syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=43
  91. en:adrenocortical hypofunction, chronic primary congenital --- r_associated #0: 42 --> en:microvillus inclusion disease
    n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=42
  92. en:coeliac disease --- r_associated #0: 42 --> en:microvillus inclusion disease
    n1=en:coeliac disease | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=42
  93. en:congenital analbuminemia --- r_associated #0: 42 --> en:microvillus inclusion disease
    n1=en:congenital analbuminemia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=42
  94. en:congenital blepharophimosis of upper eyelid --- r_associated #0: 42 --> en:microvillus inclusion disease
    n1=en:congenital blepharophimosis of upper eyelid | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=42
  95. en:disorder of jejunum --- r_associated #0: 42 --> en:microvillus inclusion disease
    n1=en:disorder of jejunum | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=42
  96. en:gluten sensitivity --- r_associated #0: 42 --> en:microvillus inclusion disease
    n1=en:gluten sensitivity | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=42
  97. maladie de whipple --- r_associated #0: 42 --> en:microvillus inclusion disease
    n1=maladie de whipple | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=42
  98. polypose rectocolique --- r_associated #0: 42 --> en:microvillus inclusion disease
    n1=polypose rectocolique | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=42
  99. en:enteronitis --- r_associated #0: 41 --> en:microvillus inclusion disease
    n1=en:enteronitis | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=41
  100. en:postcholecystectomy diarrhea --- r_associated #0: 41 --> en:microvillus inclusion disease
    n1=en:postcholecystectomy diarrhea | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=41
  101. polypose adénomateuse familiale --- r_associated #0: 41 --> en:microvillus inclusion disease
    n1=polypose adénomateuse familiale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=41
  102. polypose recto-colique familiale --- r_associated #0: 41 --> en:microvillus inclusion disease
    n1=polypose recto-colique familiale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=41
  103. polypose rectocolique familiale --- r_associated #0: 41 --> en:microvillus inclusion disease
    n1=polypose rectocolique familiale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=41
  104. Diverticule de Meckel --- r_associated #0: 40 --> en:microvillus inclusion disease
    n1=Diverticule de Meckel | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=40
  105. Whipple (maladie de) --- r_associated #0: 40 --> en:microvillus inclusion disease
    n1=Whipple (maladie de) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=40
  106. dysplasie olfacto-génitale --- r_associated #0: 40 --> en:microvillus inclusion disease
    n1=dysplasie olfacto-génitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=40
  107. intolérance au lactose --- r_associated #0: 40 --> en:microvillus inclusion disease
    n1=intolérance au lactose | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=40
  108. myofibromatose infantile --- r_associated #0: 40 --> en:microvillus inclusion disease
    n1=myofibromatose infantile | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=40
  109. en:Williams syndrome --- r_associated #0: 39 --> en:microvillus inclusion disease
    n1=en:Williams syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=39
  110. en:rotation of tooth --- r_associated #0: 39 --> en:microvillus inclusion disease
    n1=en:rotation of tooth | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=39
  111. en:williams syndrome --- r_associated #0: 39 --> en:microvillus inclusion disease
    n1=en:williams syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=39
  112. maladie coeliaque de l'enfant --- r_associated #0: 39 --> en:microvillus inclusion disease
    n1=maladie coeliaque de l'enfant | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=39
  113. en:anorectal agenesis --- r_associated #0: 38 --> en:microvillus inclusion disease
    n1=en:anorectal agenesis | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=38
  114. en:carbohydrate intolerance --- r_associated #0: 38 --> en:microvillus inclusion disease
    n1=en:carbohydrate intolerance | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=38
  115. en:congenital cardiovascular disorder --- r_associated #0: 38 --> en:microvillus inclusion disease
    n1=en:congenital cardiovascular disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=38
  116. en:small intestinal ulcer --- r_associated #0: 38 --> en:microvillus inclusion disease
    n1=en:small intestinal ulcer | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=38
  117. hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale --- r_associated #0: 38 --> en:microvillus inclusion disease
    n1=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=38
  118. en:chronic pseudo-obstruction of small intestine --- r_associated #0: 37 --> en:microvillus inclusion disease
    n1=en:chronic pseudo-obstruction of small intestine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=37
  119. en:infantile myofibromatosis --- r_associated #0: 37 --> en:microvillus inclusion disease
    n1=en:infantile myofibromatosis | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=37
  120. en:true cleft of common atrioventricular valve leaflet --- r_associated #0: 37 --> en:microvillus inclusion disease
    n1=en:true cleft of common atrioventricular valve leaflet | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=37
  121. en:truncal valve overriding ventricular septum --- r_associated #0: 37 --> en:microvillus inclusion disease
    n1=en:truncal valve overriding ventricular septum | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=37
  122. en:childhood celiac disease --- r_associated #0: 36 --> en:microvillus inclusion disease
    n1=en:childhood celiac disease | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=36
  123. en:congenital cardiac failure --- r_associated #0: 36 --> en:microvillus inclusion disease
    n1=en:congenital cardiac failure | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=36
  124. en:congenital plasminogen activator inhibitor deficiency type 1 --- r_associated #0: 36 --> en:microvillus inclusion disease
    n1=en:congenital plasminogen activator inhibitor deficiency type 1 | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=36
  125. en:imperforate anus --- r_associated #0: 36 --> en:microvillus inclusion disease
    n1=en:imperforate anus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=36
  126. en:kallmann syndrome --- r_associated #0: 36 --> en:microvillus inclusion disease
    n1=en:kallmann syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=36
  127. gluten (intolérance au) --- r_associated #0: 36 --> en:microvillus inclusion disease
    n1=gluten (intolérance au) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=36
  128. imperforation anale --- r_associated #0: 36 --> en:microvillus inclusion disease
    n1=imperforation anale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=36
  129. imperforation de l'anus --- r_associated #0: 36 --> en:microvillus inclusion disease
    n1=imperforation de l'anus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=36
  130. porphyrie érythropoïétique --- r_associated #0: 36 --> en:microvillus inclusion disease
    n1=porphyrie érythropoïétique | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=36
  131. en:congenital dysarthria --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:congenital dysarthria | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  132. en:congenital nervous system disorder --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:congenital nervous system disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  133. en:congenital oral/facial/cranial defect --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:congenital oral/facial/cranial defect | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  134. en:congenital pancreatic trypsin deficiency --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:congenital pancreatic trypsin deficiency | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  135. en:congenital quadriplegia --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:congenital quadriplegia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  136. en:congenital skeletal disorder --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:congenital skeletal disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  137. en:digeorge syndrome --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:digeorge syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  138. en:diphyllobothrium latum infection --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:diphyllobothrium latum infection | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  139. en:focal segmental ischemia of small intestine --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:focal segmental ischemia of small intestine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  140. en:gastrointestinal malabsorption syndrome co-occurrent with human immunodeficiency virus infection --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:gastrointestinal malabsorption syndrome co-occurrent with human immunodeficiency virus infection | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  141. en:intestinal atresia --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:intestinal atresia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  142. en:intestinal disaccharidase deficiency and disaccharide malabsorption --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:intestinal disaccharidase deficiency and disaccharide malabsorption | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  143. en:lactose intolerance --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:lactose intolerance | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  144. en:large intestine atresia --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:large intestine atresia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  145. en:megaloblastic anemia due to disease of small intestine --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:megaloblastic anemia due to disease of small intestine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  146. en:pigmented paravenous chorioretinal atrophy --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:pigmented paravenous chorioretinal atrophy | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  147. en:pseudomonas pyocyaneus congenital infection --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:pseudomonas pyocyaneus congenital infection | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  148. en:small intestinal hamartoma --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:small intestinal hamartoma | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  149. en:small intestinal obstruction --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:small intestinal obstruction | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  150. en:small intestine anastomotic leak --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:small intestine anastomotic leak | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  151. en:tooth malformation --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:tooth malformation | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  152. en:vacterl association --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:vacterl association | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  153. en:villous atrophy of intestine --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=en:villous atrophy of intestine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  154. mucolipidose --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=mucolipidose | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  155. rétinite pigmentaire paraveineuse --- r_associated #0: 35 --> en:microvillus inclusion disease
    n1=rétinite pigmentaire paraveineuse | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35
  156. diverticule de meckel --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=diverticule de meckel | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  157. en:acquired fructose intolerance --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:acquired fructose intolerance | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  158. en:congenital amegakaryocytic thrombocytopenia --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:congenital amegakaryocytic thrombocytopenia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  159. en:congenital anomaly of stomach --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:congenital anomaly of stomach | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  160. en:congenital auditory imperception --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:congenital auditory imperception | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  161. en:congenital blocked tear duct --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:congenital blocked tear duct | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  162. en:congenital chloride diarrhea --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:congenital chloride diarrhea | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  163. en:congenital factor ix deficiency without inhibitor --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:congenital factor ix deficiency without inhibitor | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  164. en:congenital gastrointestinal-urinary tract fistula --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:congenital gastrointestinal-urinary tract fistula | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  165. en:congenital megaprepuce --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:congenital megaprepuce | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  166. en:congenital metabolic disorder --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:congenital metabolic disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  167. en:congenital uremia --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:congenital uremia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  168. en:erythropoietic porphyria --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:erythropoietic porphyria | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  169. en:extensive congenital erosions, vesicles and reticulate scarring --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:extensive congenital erosions, vesicles and reticulate scarring | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  170. en:fetal congenital tumor causing disproportion --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:fetal congenital tumor causing disproportion | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  171. en:fordyce's disease --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:fordyce's disease | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  172. en:malabsorption syndrome --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:malabsorption syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  173. en:right atrial endocardial fibroelastosis --- r_associated #0: 34 --> en:microvillus inclusion disease
    n1=en:right atrial endocardial fibroelastosis | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=34
  174. en:anastomotic necrosis of small intestine --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:anastomotic necrosis of small intestine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  175. en:bile acid malabsorption syndrome --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:bile acid malabsorption syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  176. en:collagenous sprue --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:collagenous sprue | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  177. en:congenital and developmental myasthenia --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:congenital and developmental myasthenia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  178. en:congenital brain damage --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:congenital brain damage | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  179. en:congenital factor ix deficiency with inhibitor --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:congenital factor ix deficiency with inhibitor | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  180. en:congenital malignant melanoma --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:congenital malignant melanoma | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  181. en:congenital pancreatic cyst --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:congenital pancreatic cyst | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  182. en:duodenal atresia --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:duodenal atresia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  183. en:enterostomy malfunction --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:enterostomy malfunction | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  184. en:infant metachromatic leukodystrophies --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:infant metachromatic leukodystrophies | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  185. en:intestinal disorders congenital --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:intestinal disorders congenital | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  186. en:lactose intolerance, adult type --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:lactose intolerance, adult type | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  187. en:mucolipidosis --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:mucolipidosis | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  188. en:muir-torre syndrome --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:muir-torre syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  189. en:persistent cloaca --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:persistent cloaca | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  190. en:right atrial appendage - left - juxtaposition --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:right atrial appendage - left - juxtaposition | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  191. en:rudimentary left ventricle --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:rudimentary left ventricle | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  192. en:shortened trunk --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:shortened trunk | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  193. en:small bowel fistula --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:small bowel fistula | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  194. en:small intestinal gangrene --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:small intestinal gangrene | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  195. en:transposition of intestine (disorder) --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=en:transposition of intestine (disorder) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  196. nystagmus congénital isolé --- r_associated #0: 32 --> en:microvillus inclusion disease
    n1=nystagmus congénital isolé | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=32
  197. en:acquired acrodermatitis enteropathica --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:acquired acrodermatitis enteropathica | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  198. en:anterior displaced anus --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:anterior displaced anus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  199. en:chemically-induced malabsorption --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:chemically-induced malabsorption | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  200. en:chronic diarrhea due to glucoamylase deficiency --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:chronic diarrhea due to glucoamylase deficiency | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  201. en:congenital blepharophimosis of lower eyelid --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:congenital blepharophimosis of lower eyelid | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  202. en:congenital constriction of pylorus --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:congenital constriction of pylorus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  203. en:congenital ear disorder --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:congenital ear disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  204. en:congenital exophthalmos --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:congenital exophthalmos | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  205. en:congenital malformation of upper alimentary tract --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:congenital malformation of upper alimentary tract | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  206. en:congenital posterior subcapsular polar cataract --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:congenital posterior subcapsular polar cataract | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  207. en:congenital retinoschisis --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:congenital retinoschisis | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  208. en:congenital sucrase-isomaltase deficiency --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:congenital sucrase-isomaltase deficiency | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  209. en:foreign body in small intestine --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:foreign body in small intestine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  210. en:hamartoma of small intestine --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:hamartoma of small intestine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  211. en:megophthalmos --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:megophthalmos | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  212. en:mobile caecum syndrome --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:mobile caecum syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  213. en:mottled teeth, congenital --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:mottled teeth, congenital | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  214. en:multiple gastrointestinal atresias (disorder) --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:multiple gastrointestinal atresias (disorder) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  215. en:neuronal intestinal dysplasia --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:neuronal intestinal dysplasia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  216. en:other congenital malformations of digestive system --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:other congenital malformations of digestive system | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  217. en:pancreatic triacylglycerol lipase deficiency --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:pancreatic triacylglycerol lipase deficiency | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  218. en:vitello-intestinal duct remnant --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=en:vitello-intestinal duct remnant | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  219. polypose familiale du côlon --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=polypose familiale du côlon | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  220. syndrome de malabsorption --- r_associated #0: 31 --> en:microvillus inclusion disease
    n1=syndrome de malabsorption | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=31
  221. Maladie de Whipple --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=Maladie de Whipple | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  222. contractures congénitales et arachnodactylie --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=contractures congénitales et arachnodactylie | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  223. en:acute pseudo-obstruction of small intestine --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:acute pseudo-obstruction of small intestine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  224. en:beckwith-wiedemann syndrome --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:beckwith-wiedemann syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  225. en:bile acid malabsorption --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:bile acid malabsorption | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  226. en:choledochal cyst --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:choledochal cyst | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  227. en:chronic steatorrhea --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:chronic steatorrhea | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  228. en:congenital absence of alimentary tract --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:congenital absence of alimentary tract | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  229. en:congenital anomaly of digestive organ --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:congenital anomaly of digestive organ | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  230. en:congenital anomaly of intestinal tract --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:congenital anomaly of intestinal tract | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  231. en:congenital atrophy of left lobe of liver --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:congenital atrophy of left lobe of liver | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  232. en:congenital dysphasia --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:congenital dysphasia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  233. en:congenital hearing disorder --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:congenital hearing disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  234. en:congenital melanocytic nevus of trunk --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:congenital melanocytic nevus of trunk | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  235. en:congenital palato-esophageal incoordination --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:congenital palato-esophageal incoordination | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  236. en:congenital pseudoporencephaly --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:congenital pseudoporencephaly | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  237. en:congenital reproductive system disorder --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:congenital reproductive system disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  238. en:congenital stenosis --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:congenital stenosis | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  239. en:dental arch length loss secondary to congenitally missing teeth --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:dental arch length loss secondary to congenitally missing teeth | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  240. en:developmental fault --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:developmental fault | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  241. en:disaccharide metabolism disorder --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:disaccharide metabolism disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  242. en:other specified congenital malformations of digestive system --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:other specified congenital malformations of digestive system | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  243. en:parachute malformation of right atrioventricular valve --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:parachute malformation of right atrioventricular valve | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  244. en:small intestinal infarction --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:small intestinal infarction | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  245. en:steatorrhea --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=en:steatorrhea | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  246. malformation oculaire --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=malformation oculaire | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  247. polyadénomatose recto-colique familiale --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=polyadénomatose recto-colique familiale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  248. syndrome de Williams --- r_associated #0: 30 --> en:microvillus inclusion disease
    n1=syndrome de Williams | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=30
  249. en:acquired lactase deficiency --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:acquired lactase deficiency | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  250. en:adenomatosis coli --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:adenomatosis coli | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  251. en:barrett esophagus --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:barrett esophagus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  252. en:congenital complete atrioventricular block --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:congenital complete atrioventricular block | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  253. en:congenital facial asymmetry --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:congenital facial asymmetry | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  254. en:congenital factor ix deficiency variant --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:congenital factor ix deficiency variant | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  255. en:congenital neurogenic ileus syndrome --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:congenital neurogenic ileus syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  256. en:disorder of ileum --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:disorder of ileum | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  257. en:enterokinase deficiency --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:enterokinase deficiency | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  258. en:hiv enteropathy --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:hiv enteropathy | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  259. en:intestinal malrotation --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:intestinal malrotation | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  260. en:lymphangiectasia intestinal congenital --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:lymphangiectasia intestinal congenital | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  261. en:palmoplantar porokeratosis --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:palmoplantar porokeratosis | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  262. en:post-gastrointestinal tract surgery malnutrition --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:post-gastrointestinal tract surgery malnutrition | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  263. en:right atrial appendage absent --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:right atrial appendage absent | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  264. en:small intestine atresia --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:small intestine atresia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  265. en:spinal hydromeningocele --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:spinal hydromeningocele | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  266. en:toxemic infantilism --- r_associated #0: 29 --> en:microvillus inclusion disease
    n1=en:toxemic infantilism | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=29
  267. créatorrhée --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=créatorrhée | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  268. en:amyloidosis of small intestine --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:amyloidosis of small intestine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  269. en:anal imperforation --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:anal imperforation | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  270. en:autoimmune enteropathy --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:autoimmune enteropathy | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  271. en:cap myopathy --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:cap myopathy | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  272. en:congenital connective tissue disorder --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:congenital connective tissue disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  273. en:congenital end-plate acetylcholinesterase deficiency --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:congenital end-plate acetylcholinesterase deficiency | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  274. en:congenital esotropia --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:congenital esotropia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  275. en:congenital fibrinogen abnormality --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:congenital fibrinogen abnormality | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  276. en:congenital hepatic porphyria --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:congenital hepatic porphyria | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  277. en:congenital immunodeficiency disease --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:congenital immunodeficiency disease | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  278. en:congenital intestinal obstruction --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:congenital intestinal obstruction | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  279. en:congenital laryngeal cyst --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:congenital laryngeal cyst | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  280. en:congenital leptin deficiency --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:congenital leptin deficiency | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  281. en:congenital skin contracture --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:congenital skin contracture | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  282. en:congenital velopharyngeal dysfunction --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:congenital velopharyngeal dysfunction | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  283. en:congenital/genetic syndrome with poikiloderma --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:congenital/genetic syndrome with poikiloderma | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  284. en:esophageal atresia --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:esophageal atresia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  285. en:gastrointestinal vessel anomaly --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:gastrointestinal vessel anomaly | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  286. en:lactase deficiency (disorder) --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:lactase deficiency (disorder) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  287. en:microcolon --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:microcolon | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  288. en:other specified congenital malformations of upper alimentary tract --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:other specified congenital malformations of upper alimentary tract | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  289. en:pernicious anemia --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:pernicious anemia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  290. en:primary malabsorption of infancy --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:primary malabsorption of infancy | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  291. en:small bowel bacterial overgrowth syndrome --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:small bowel bacterial overgrowth syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  292. en:vitamin d-dependent rickets, type 2 --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:vitamin d-dependent rickets, type 2 | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  293. en:zinc-deficiency type --- r_associated #0: 28 --> en:microvillus inclusion disease
    n1=en:zinc-deficiency type | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=28
  294. en:congenital anomaly of esophagus --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:congenital anomaly of esophagus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  295. en:congenital anomaly of small intestine --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:congenital anomaly of small intestine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  296. en:congenital cyst of aryepiglottic fold --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:congenital cyst of aryepiglottic fold | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  297. en:congenital duplication of appendix --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:congenital duplication of appendix | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  298. en:congenital fecaliths --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:congenital fecaliths | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  299. en:congenital hypothyroidism --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:congenital hypothyroidism | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  300. en:congenital kyphosis --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:congenital kyphosis | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  301. en:diaphragm disease of intestine --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:diaphragm disease of intestine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  302. en:duodenal diseases --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:duodenal diseases | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  303. en:hereditary non-polyposis colorectal cancer syndrome --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:hereditary non-polyposis colorectal cancer syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  304. en:hill diarrhea --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:hill diarrhea | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  305. en:intestinal pseudo-obstruction --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:intestinal pseudo-obstruction | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  306. en:microvillus alteration --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:microvillus alteration | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  307. en:parachute malformation of common atrioventricular valve --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:parachute malformation of common atrioventricular valve | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  308. en:regional congenital anomaly --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=en:regional congenital anomaly | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  309. intestin irritable (syndrome de l') --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=intestin irritable (syndrome de l') | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  310. malformation --- r_associated #0: 27 --> en:microvillus inclusion disease
    n1=malformation | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=27
  311. Maladie congénitale --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=Maladie congénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  312. en:chromosomal aberration --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:chromosomal aberration | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  313. en:congenital anomaly of gastrointestinal tract --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:congenital anomaly of gastrointestinal tract | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  314. en:congenital choroidal fold --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:congenital choroidal fold | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  315. en:congenital claw toe --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:congenital claw toe | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  316. en:congenital digestive system disorder --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:congenital digestive system disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  317. en:congenital intestinal malformation --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:congenital intestinal malformation | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  318. en:congenital monosaccharide malabsorption --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:congenital monosaccharide malabsorption | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  319. en:congenital pain insensitivity --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:congenital pain insensitivity | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  320. en:congenital vascular disorder --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:congenital vascular disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  321. en:developmental anomaly --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:developmental anomaly | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  322. en:diverticulosis of small intestine --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:diverticulosis of small intestine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  323. en:enterospasm --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:enterospasm | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  324. en:hereditary hemorrhagic telangiectasia --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:hereditary hemorrhagic telangiectasia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  325. en:hutch diverticulum --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:hutch diverticulum | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  326. en:hyperhomocysteinemia --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:hyperhomocysteinemia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  327. en:hypopituitarism --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:hypopituitarism | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  328. en:nystagmus --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:nystagmus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  329. en:parachute malformation of left atrioventricular valve --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:parachute malformation of left atrioventricular valve | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  330. en:postprocedural steatorrhea --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:postprocedural steatorrhea | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  331. en:small bowel adhesions --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:small bowel adhesions | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  332. en:small intestinal stasis syndrome --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:small intestinal stasis syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  333. en:sucrose intolerance --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=en:sucrose intolerance | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  334. entérospasme --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=entérospasme | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  335. intolérance au saccharose --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=intolérance au saccharose | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  336. maladie c?liaque --- r_associated #0: 26 --> en:microvillus inclusion disease
    n1=maladie c?liaque | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=26
  337. dysplasie olfactogénitale --- r_associated #0: 25 --> en:microvillus inclusion disease
    n1=dysplasie olfactogénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=25
  338. en:buphthalmia --- r_associated #0: 25 --> en:microvillus inclusion disease
    n1=en:buphthalmia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=25
  339. en:lymphangiectasis, intestinal --- r_associated #0: 25 --> en:microvillus inclusion disease
    n1=en:lymphangiectasis, intestinal | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=25
  340. en:proctatresia --- r_associated #0: 25 --> en:microvillus inclusion disease
    n1=en:proctatresia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=25
  341. hypogonadisme avec anosmie --- r_associated #0: 25 --> en:microvillus inclusion disease
    n1=hypogonadisme avec anosmie | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=25
  342. hypopituitarisme --- r_associated #0: 25 --> en:microvillus inclusion disease
    n1=hypopituitarisme | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=25
  343. acrodermatitis enteropathica --- r_associated #0: 24 --> en:microvillus inclusion disease
    n1=acrodermatitis enteropathica | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=24
  344. en:Günther's disease --- r_associated #0: 24 --> en:microvillus inclusion disease
    n1=en:Günther's disease | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=24
  345. en:erythropoietic uroporphyria --- r_associated #0: 24 --> en:microvillus inclusion disease
    n1=en:erythropoietic uroporphyria | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=24
  346. en:galactosemia --- r_associated #0: 24 --> en:microvillus inclusion disease
    n1=en:galactosemia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=24
  347. en:intestinal infantilism --- r_associated #0: 24 --> en:microvillus inclusion disease
    n1=en:intestinal infantilism | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=24
  348. méthémoglobinémie héréditaire --- r_associated #0: 24 --> en:microvillus inclusion disease
    n1=méthémoglobinémie héréditaire | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=24
  349. une anomalie congénitale --- r_associated #0: 24 --> en:microvillus inclusion disease
    n1=une anomalie congénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=24
  350. Sprengel (syndrome de) --- r_associated #0: 23 --> en:microvillus inclusion disease
    n1=Sprengel (syndrome de) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=23
  351. déficit congénital en mégacaryocytes --- r_associated #0: 23 --> en:microvillus inclusion disease
    n1=déficit congénital en mégacaryocytes | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=23
  352. en:congenital anomaly of salivary gland --- r_associated #0: 23 --> en:microvillus inclusion disease
    n1=en:congenital anomaly of salivary gland | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=23
  353. en:congenital biliary tract disorder --- r_associated #0: 23 --> en:microvillus inclusion disease
    n1=en:congenital biliary tract disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=23
  354. en:amyoplasia congenita --- r_associated #0: 22 --> en:microvillus inclusion disease
    n1=en:amyoplasia congenita | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=22
  355. en:congenital disease of brain --- r_associated #0: 22 --> en:microvillus inclusion disease
    n1=en:congenital disease of brain | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=22
  356. en:congenital kidney disorder --- r_associated #0: 22 --> en:microvillus inclusion disease
    n1=en:congenital kidney disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=22
  357. en:hypothalamic hamartoblastoma --- r_associated #0: 22 --> en:microvillus inclusion disease
    n1=en:hypothalamic hamartoblastoma | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=22
  358. en:polyposis coli --- r_associated #0: 22 --> en:microvillus inclusion disease
    n1=en:polyposis coli | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=22
  359. anus ectopique --- r_associated #0: 21 --> en:microvillus inclusion disease
    n1=anus ectopique | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=21
  360. buphtalmie --- r_associated #0: 21 --> en:microvillus inclusion disease
    n1=buphtalmie | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=21
  361. en:Fordyce's disease --- r_associated #0: 21 --> en:microvillus inclusion disease
    n1=en:Fordyce's disease | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=21
  362. en:blind loop syndrome --- r_associated #0: 21 --> en:microvillus inclusion disease
    n1=en:blind loop syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=21
  363. en:congenital porphyria --- r_associated #0: 21 --> en:microvillus inclusion disease
    n1=en:congenital porphyria | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=21
  364. en:gluten intolerance --- r_associated #0: 21 --> en:microvillus inclusion disease
    n1=en:gluten intolerance | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=21
  365. en:hirschsprung disease --- r_associated #0: 21 --> en:microvillus inclusion disease
    n1=en:hirschsprung disease | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=21
  366. en:peutz-jeghers syndrome --- r_associated #0: 21 --> en:microvillus inclusion disease
    n1=en:peutz-jeghers syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=21
  367. en:satoyoshi syndrome --- r_associated #0: 21 --> en:microvillus inclusion disease
    n1=en:satoyoshi syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=21
  368. idiosyncrasie au fructose --- r_associated #0: 21 --> en:microvillus inclusion disease
    n1=idiosyncrasie au fructose | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=21
  369. polyadénomatose rectocolique familiale --- r_associated #0: 21 --> en:microvillus inclusion disease
    n1=polyadénomatose rectocolique familiale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=21
  370. syndrome de Prader-Willi --- r_associated #0: 21 --> en:microvillus inclusion disease
    n1=syndrome de Prader-Willi | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=21
  371. ARTHROGRYPOSE --- r_associated #0: 20 --> en:microvillus inclusion disease
    n1=ARTHROGRYPOSE | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=20
  372. Vestige du conduit vitellin --- r_associated #0: 20 --> en:microvillus inclusion disease
    n1=Vestige du conduit vitellin | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=20
  373. dysplasie olfactogénitale de De Morsier --- r_associated #0: 20 --> en:microvillus inclusion disease
    n1=dysplasie olfactogénitale de De Morsier | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=20
  374. maladie --- r_associated #0: 20 --> en:microvillus inclusion disease
    n1=maladie | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=20
  375. Arthrogrypose --- r_associated #0: 15 --> en:microvillus inclusion disease
    n1=Arthrogrypose | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=15
  376. Atrésie de l'œsophage --- r_associated #0: 15 --> en:microvillus inclusion disease
    n1=Atrésie de l'œsophage | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=15
  377. BNV --- r_associated #0: 15 --> en:microvillus inclusion disease
    n1=BNV | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=15
  378. Intolérance au fructose --- r_associated #0: 15 --> en:microvillus inclusion disease
    n1=Intolérance au fructose | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=15
  379. Intolérance au saccharose --- r_associated #0: 15 --> en:microvillus inclusion disease
    n1=Intolérance au saccharose | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=15
  380. Kallman --- r_associated #0: 15 --> en:microvillus inclusion disease
    n1=Kallman | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=15
  381. Malformation congénitale --- r_associated #0: 15 --> en:microvillus inclusion disease
    n1=Malformation congénitale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=15
  382. diverticulaire (maladie) --- r_associated #0: 15 --> en:microvillus inclusion disease
    n1=diverticulaire (maladie) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=15
  383. malentendant (enfant) --- r_associated #0: 15 --> en:microvillus inclusion disease
    n1=malentendant (enfant) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=15
  384. syndrome de Kallman-de Morsier --- r_associated #0: 15 --> en:microvillus inclusion disease
    n1=syndrome de Kallman-de Morsier | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=15
  385. syndrome de de Morsier-Kallmann --- r_associated #0: 15 --> en:microvillus inclusion disease
    n1=syndrome de de Morsier-Kallmann | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=15
  386. Anomalie chromosomique --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=Anomalie chromosomique | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  387. CONGÉNITALE --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=CONGÉNITALE | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  388. Entérite --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=Entérite | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  389. Haltia-Santavuori (maladie de) --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=Haltia-Santavuori (maladie de) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  390. Malabsorption --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=Malabsorption | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  391. Malformation --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=Malformation | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  392. Syndrome de Prader-Willi --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=Syndrome de Prader-Willi | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  393. Syndrome de malabsorption --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=Syndrome de malabsorption | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  394. aberration chromosomique --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=aberration chromosomique | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  395. anémie pernicieuse --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=anémie pernicieuse | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  396. canal d'alimentation --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=canal d'alimentation | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  397. canal de coulée --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=canal de coulée | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  398. en:Gee's disease --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:Gee's disease | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  399. en:Herter's disease --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:Herter's disease | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  400. en:PWS --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:PWS | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  401. en:WBS --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:WBS | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  402. en:Williams' syndrome --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:Williams' syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  403. en:Williams-Beuren syndrome --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:Williams-Beuren syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  404. en:and postaxil polydactylie --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:and postaxil polydactylie | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  405. en:atresia ani --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:atresia ani | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  406. en:buphtalmia --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:buphtalmia | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  407. en:buphthalmos --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:buphthalmos | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  408. en:buphthalmus --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:buphthalmus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  409. en:cacomorphosis --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:cacomorphosis | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  410. en:celiac affection --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:celiac affection | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  411. en:celiac disease --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:celiac disease | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  412. en:celiac sprue --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:celiac sprue | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  413. en:chromosomal disorder --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:chromosomal disorder | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  414. en:contractural arachnodactyly --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:contractural arachnodactyly | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  415. en:diverticular disease --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:diverticular disease | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  416. en:heubner-herter disease --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:heubner-herter disease | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  417. en:hypoacousic child --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:hypoacousic child | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  418. en:intestinal malabsorption --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:intestinal malabsorption | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  419. en:irritable bowel syndrome --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=en:irritable bowel syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  420. glutine --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=glutine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  421. gluténine --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=gluténine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  422. gly --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=gly | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  423. glycanne --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=glycanne | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  424. glycation --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=glycation | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  425. glycémie --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=glycémie | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  426. glycéraldéhyde --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=glycéraldéhyde | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  427. hypohypophysie --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=hypohypophysie | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  428. hypostimulinie --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=hypostimulinie | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  429. impédance acoustique (symb. Z) --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=impédance acoustique (symb. Z) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  430. nystagmus --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=nystagmus | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  431. nystagmus héréditaire vertical --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=nystagmus héréditaire vertical | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  432. nystagmus lié au sexe --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=nystagmus lié au sexe | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  433. nystagmus myoclonies --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=nystagmus myoclonies | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  434. polyphosphorique (acide) --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=polyphosphorique (acide) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  435. porphyrie (anesthésie chez un patient atteint de) --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=porphyrie (anesthésie chez un patient atteint de) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  436. rétinite pigmentaire liée à la périphérine (pro219leu) --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=rétinite pigmentaire liée à la périphérine (pro219leu) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  437. syndrome de de Morsier --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=syndrome de de Morsier | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  438. trou de coulée --- r_associated #0: 10 --> en:microvillus inclusion disease
    n1=trou de coulée | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=10
  439. diverticule de l'iléon --- r_associated #0: 6 --> en:microvillus inclusion disease
    n1=diverticule de l'iléon | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=6
  440. Hypopituitarisme --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=Hypopituitarisme | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  441. Maladie c?liaque --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=Maladie c?liaque | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  442. Williams (syndrome de) --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=Williams (syndrome de) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  443. diverticule caliciel --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=diverticule caliciel | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  444. diverticule de l'ampoule du conduit déférent --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=diverticule de l'ampoule du conduit déférent | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  445. diverticule de l'oesophage --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=diverticule de l'oesophage | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  446. diverticule de la trompe de Fallope --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=diverticule de la trompe de Fallope | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  447. diverticule de la voie excrétrice urinaire --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=diverticule de la voie excrétrice urinaire | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  448. intestin pancréatique --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=intestin pancréatique | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  449. intestin primitif --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=intestin primitif | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  450. intestinal fatty acid binding protein --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=intestinal fatty acid binding protein | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  451. intima --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=intima | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  452. intimal --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=intimal | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  453. intolérance alimentaire non organique --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=intolérance alimentaire non organique | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  454. malabsorption (syndrome de) --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=malabsorption (syndrome de) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  455. malf ormation dysraphique --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=malf ormation dysraphique | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  456. malformation kystique adénomatoïde du poumon --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=malformation kystique adénomatoïde du poumon | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  457. malformation luxante de la hanche --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=malformation luxante de la hanche | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  458. malformation mamelonnaire --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=malformation mamelonnaire | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  459. malformation mammaire --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=malformation mammaire | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  460. malformation ombilicale --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=malformation ombilicale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  461. malformation utérine --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=malformation utérine | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  462. malformation vaginale --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=malformation vaginale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  463. malformation vasculaire cérébrale du nourrisson --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=malformation vasculaire cérébrale du nourrisson | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  464. malformations de la charnière occipitocervicale --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=malformations de la charnière occipitocervicale | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  465. nystagmus (zone de moindre) --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=nystagmus (zone de moindre) | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  466. spuria --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=spuria | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  467. syndrome de Sprengel --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=syndrome de Sprengel | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
  468. syndrome olfacto-génital --- r_associated #0: 5 --> en:microvillus inclusion disease
    n1=syndrome olfacto-génital | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=5
Le service Rézo permet d'énumérer les relations existant pour un terme. Ce service est interrogeable par programme.
Projet JeuxDeMots - url: http://www.jeuxdemots.org
contact: mathieu.lafourcade@lirmm.fr