Javascript doit fonctionner ! Activez-le et rechargez cette page.
Le Rézo de JeuxDeMots
• Types de relations
• Types de noeuds
• Consolider
le terme
  Options  
             

  Filtrage type relations : +   - (ex: 4, 12, 18, 36, 444, 555, 777)
  Filtrage valeur :          min   max
  Filtrage type noeuds :   +   - (ex: 4, 6, 8, 9, 10, 12, 18, 36, 444, 555, 777)

  Présentation de sortie :   (ex: -rien-, cloud, nicecloud)
 

'en:peutz-jeghers syndrome'
(id=6809093 ; fe=en:peutz-jeghers syndrome ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=61167 creation date=2017-06-25 touchdate=2025-12-21 13:22:43.000)
≈ 1149 relations sortantes

  1. en:peutz-jeghers syndrome -- r_associated #0: 52 / 1 -> syndrome de peutz-jeghers
    n1=en:peutz-jeghers syndrome | n2=syndrome de peutz-jeghers | rel=r_associated | relid=0 | w=52
  2. en:peutz-jeghers syndrome -- r_associated #0: 47 / 0.904 -> polypose hamartomateuse intestinale
    n1=en:peutz-jeghers syndrome | n2=polypose hamartomateuse intestinale | rel=r_associated | relid=0 | w=47
  3. en:peutz-jeghers syndrome -- r_associated #0: 46 / 0.885 -> lentiginose périorificielle avec polypose viscérale
    n1=en:peutz-jeghers syndrome | n2=lentiginose périorificielle avec polypose viscérale | rel=r_associated | relid=0 | w=46
  4. en:peutz-jeghers syndrome -- r_associated #0: 45 / 0.865 -> polypose intestinale pigmentation cutanée
    n1=en:peutz-jeghers syndrome | n2=polypose intestinale pigmentation cutanée | rel=r_associated | relid=0 | w=45
  5. en:peutz-jeghers syndrome -- r_associated #0: 43 / 0.827 -> en:lentigo simplex
    n1=en:peutz-jeghers syndrome | n2=en:lentigo simplex | rel=r_associated | relid=0 | w=43
  6. en:peutz-jeghers syndrome -- r_associated #0: 42 / 0.808 -> en:skin hyperpigmentation
    n1=en:peutz-jeghers syndrome | n2=en:skin hyperpigmentation | rel=r_associated | relid=0 | w=42
  7. en:peutz-jeghers syndrome -- r_associated #0: 42 / 0.808 -> syndrome de Peutz-Jeghers
    n1=en:peutz-jeghers syndrome | n2=syndrome de Peutz-Jeghers | rel=r_associated | relid=0 | w=42
  8. en:peutz-jeghers syndrome -- r_associated #0: 40 / 0.769 -> en:gastric hemangioma
    n1=en:peutz-jeghers syndrome | n2=en:gastric hemangioma | rel=r_associated | relid=0 | w=40
  9. en:peutz-jeghers syndrome -- r_associated #0: 39 / 0.75 -> en:carney complex
    n1=en:peutz-jeghers syndrome | n2=en:carney complex | rel=r_associated | relid=0 | w=39
  10. en:peutz-jeghers syndrome -- r_associated #0: 38 / 0.731 -> en:congenital melanosis
    n1=en:peutz-jeghers syndrome | n2=en:congenital melanosis | rel=r_associated | relid=0 | w=38
  11. en:peutz-jeghers syndrome -- r_associated #0: 37 / 0.712 -> en:blepharal pigmentation
    n1=en:peutz-jeghers syndrome | n2=en:blepharal pigmentation | rel=r_associated | relid=0 | w=37
  12. en:peutz-jeghers syndrome -- r_associated #0: 37 / 0.712 -> en:generalized hyperpigmentation
    n1=en:peutz-jeghers syndrome | n2=en:generalized hyperpigmentation | rel=r_associated | relid=0 | w=37
  13. en:peutz-jeghers syndrome -- r_associated #0: 37 / 0.712 -> en:intestinal polyps
    n1=en:peutz-jeghers syndrome | n2=en:intestinal polyps | rel=r_associated | relid=0 | w=37
  14. en:peutz-jeghers syndrome -- r_associated #0: 37 / 0.712 -> en:irregular hyperpigmentation
    n1=en:peutz-jeghers syndrome | n2=en:irregular hyperpigmentation | rel=r_associated | relid=0 | w=37
  15. en:peutz-jeghers syndrome -- r_associated #0: 36 / 0.692 -> en:congenital intestinal malformation
    n1=en:peutz-jeghers syndrome | n2=en:congenital intestinal malformation | rel=r_associated | relid=0 | w=36
  16. en:peutz-jeghers syndrome -- r_associated #0: 36 / 0.692 -> en:gastrointestinal neoplasms benign nec
    n1=en:peutz-jeghers syndrome | n2=en:gastrointestinal neoplasms benign nec | rel=r_associated | relid=0 | w=36
  17. en:peutz-jeghers syndrome -- r_associated #0: 35 / 0.673 -> en:intestinal angioma
    n1=en:peutz-jeghers syndrome | n2=en:intestinal angioma | rel=r_associated | relid=0 | w=35
  18. en:peutz-jeghers syndrome -- r_associated #0: 34 / 0.654 -> en:hyperbilirubinemia
    n1=en:peutz-jeghers syndrome | n2=en:hyperbilirubinemia | rel=r_associated | relid=0 | w=34
  19. en:peutz-jeghers syndrome -- r_associated #0: 34 / 0.654 -> en:intestinal polyposis
    n1=en:peutz-jeghers syndrome | n2=en:intestinal polyposis | rel=r_associated | relid=0 | w=34
  20. en:peutz-jeghers syndrome -- r_associated #0: 34 / 0.654 -> en:intra-abdominal hemangioma
    n1=en:peutz-jeghers syndrome | n2=en:intra-abdominal hemangioma | rel=r_associated | relid=0 | w=34
  21. en:peutz-jeghers syndrome -- r_associated #0: 34 / 0.654 -> en:vitiligo
    n1=en:peutz-jeghers syndrome | n2=en:vitiligo | rel=r_associated | relid=0 | w=34
  22. en:peutz-jeghers syndrome -- r_associated #0: 32 / 0.615 -> en:benign pancreatic neoplasm
    n1=en:peutz-jeghers syndrome | n2=en:benign pancreatic neoplasm | rel=r_associated | relid=0 | w=32
  23. en:peutz-jeghers syndrome -- r_associated #0: 32 / 0.615 -> en:cloacal exstrophy
    n1=en:peutz-jeghers syndrome | n2=en:cloacal exstrophy | rel=r_associated | relid=0 | w=32
  24. en:peutz-jeghers syndrome -- r_associated #0: 32 / 0.615 -> en:congenital anomaly of stomach
    n1=en:peutz-jeghers syndrome | n2=en:congenital anomaly of stomach | rel=r_associated | relid=0 | w=32
  25. en:peutz-jeghers syndrome -- r_associated #0: 32 / 0.615 -> en:dolichocolon
    n1=en:peutz-jeghers syndrome | n2=en:dolichocolon | rel=r_associated | relid=0 | w=32
  26. en:peutz-jeghers syndrome -- r_associated #0: 32 / 0.615 -> en:freckles
    n1=en:peutz-jeghers syndrome | n2=en:freckles | rel=r_associated | relid=0 | w=32
  27. en:peutz-jeghers syndrome -- r_associated #0: 32 / 0.615 -> en:small intestinal polyposis
    n1=en:peutz-jeghers syndrome | n2=en:small intestinal polyposis | rel=r_associated | relid=0 | w=32
  28. en:peutz-jeghers syndrome -- r_associated #0: 31 / 0.596 -> en:congenital anomaly of gastrointestinal tract
    n1=en:peutz-jeghers syndrome | n2=en:congenital anomaly of gastrointestinal tract | rel=r_associated | relid=0 | w=31
  29. en:peutz-jeghers syndrome -- r_associated #0: 31 / 0.596 -> en:melanocytic hyperplasia
    n1=en:peutz-jeghers syndrome | n2=en:melanocytic hyperplasia | rel=r_associated | relid=0 | w=31
  30. en:peutz-jeghers syndrome -- r_associated #0: 31 / 0.596 -> en:syndrome
    n1=en:peutz-jeghers syndrome | n2=en:syndrome | rel=r_associated | relid=0 | w=31
  31. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:alpha-1 antitrypsin deficiency
    n1=en:peutz-jeghers syndrome | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=30
  32. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:atrophic myositis
    n1=en:peutz-jeghers syndrome | n2=en:atrophic myositis | rel=r_associated | relid=0 | w=30
  33. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:atrophoderma vermiculatum
    n1=en:peutz-jeghers syndrome | n2=en:atrophoderma vermiculatum | rel=r_associated | relid=0 | w=30
  34. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:atrophy of liver
    n1=en:peutz-jeghers syndrome | n2=en:atrophy of liver | rel=r_associated | relid=0 | w=30
  35. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:autosomal dominant analbuminemia
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant analbuminemia | rel=r_associated | relid=0 | w=30
  36. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:autosomal dominant hyperinsulinism due to kir6.2 deficiency
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | rel=r_associated | relid=0 | w=30
  37. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:autosomal recessive idiopathic familial dystonia
    n1=en:peutz-jeghers syndrome | n2=en:autosomal recessive idiopathic familial dystonia | rel=r_associated | relid=0 | w=30
  38. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:beckwith-wiedemann syndrome
    n1=en:peutz-jeghers syndrome | n2=en:beckwith-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  39. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:behavioral variant of frontotemporal dementia
    n1=en:peutz-jeghers syndrome | n2=en:behavioral variant of frontotemporal dementia | rel=r_associated | relid=0 | w=30
  40. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:benign peritoneal neoplasm
    n1=en:peutz-jeghers syndrome | n2=en:benign peritoneal neoplasm | rel=r_associated | relid=0 | w=30
  41. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:benign small intestinal neoplasm
    n1=en:peutz-jeghers syndrome | n2=en:benign small intestinal neoplasm | rel=r_associated | relid=0 | w=30
  42. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:blau syndrome
    n1=en:peutz-jeghers syndrome | n2=en:blau syndrome | rel=r_associated | relid=0 | w=30
  43. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:brachydactyly, type a1 (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:brachydactyly, type a1 (disorder) | rel=r_associated | relid=0 | w=30
  44. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:cerebral lipidosis
    n1=en:peutz-jeghers syndrome | n2=en:cerebral lipidosis | rel=r_associated | relid=0 | w=30
  45. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:chemically induced
    n1=en:peutz-jeghers syndrome | n2=en:chemically induced | rel=r_associated | relid=0 | w=30
  46. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:chondromalacia of left knee
    n1=en:peutz-jeghers syndrome | n2=en:chondromalacia of left knee | rel=r_associated | relid=0 | w=30
  47. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:choreoathetosis/spasticity, episodic
    n1=en:peutz-jeghers syndrome | n2=en:choreoathetosis/spasticity, episodic | rel=r_associated | relid=0 | w=30
  48. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:chromosome 17q21.31 deletion syndrome
    n1=en:peutz-jeghers syndrome | n2=en:chromosome 17q21.31 deletion syndrome | rel=r_associated | relid=0 | w=30
  49. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:congenital
    n1=en:peutz-jeghers syndrome | n2=en:congenital | rel=r_associated | relid=0 | w=30
  50. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:dicer1 syndrome
    n1=en:peutz-jeghers syndrome | n2=en:dicer1 syndrome | rel=r_associated | relid=0 | w=30
  51. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:dominant autosomal hereditary disorder, complete penetrance
    n1=en:peutz-jeghers syndrome | n2=en:dominant autosomal hereditary disorder, complete penetrance | rel=r_associated | relid=0 | w=30
  52. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:dominant beta-thalassemia
    n1=en:peutz-jeghers syndrome | n2=en:dominant beta-thalassemia | rel=r_associated | relid=0 | w=30
  53. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:dystrophia myotonica 2
    n1=en:peutz-jeghers syndrome | n2=en:dystrophia myotonica 2 | rel=r_associated | relid=0 | w=30
  54. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:familial acantholysis
    n1=en:peutz-jeghers syndrome | n2=en:familial acantholysis | rel=r_associated | relid=0 | w=30
  55. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:familial hypodontia
    n1=en:peutz-jeghers syndrome | n2=en:familial hypodontia | rel=r_associated | relid=0 | w=30
  56. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:familial spontaneous pneumothorax
    n1=en:peutz-jeghers syndrome | n2=en:familial spontaneous pneumothorax | rel=r_associated | relid=0 | w=30
  57. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:game friedman paradice syndrome
    n1=en:peutz-jeghers syndrome | n2=en:game friedman paradice syndrome | rel=r_associated | relid=0 | w=30
  58. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:hereditary breast and ovarian cancer syndrome
    n1=en:peutz-jeghers syndrome | n2=en:hereditary breast and ovarian cancer syndrome | rel=r_associated | relid=0 | w=30
  59. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:hunter syndrome
    n1=en:peutz-jeghers syndrome | n2=en:hunter syndrome | rel=r_associated | relid=0 | w=30
  60. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:hypermelanosis following phototherapy for neonatal jaundice
    n1=en:peutz-jeghers syndrome | n2=en:hypermelanosis following phototherapy for neonatal jaundice | rel=r_associated | relid=0 | w=30
  61. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:hypopigmentation of eyelid
    n1=en:peutz-jeghers syndrome | n2=en:hypopigmentation of eyelid | rel=r_associated | relid=0 | w=30
  62. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:ichthyosis congenita with biliary atresia
    n1=en:peutz-jeghers syndrome | n2=en:ichthyosis congenita with biliary atresia | rel=r_associated | relid=0 | w=30
  63. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:intestinal malrotation
    n1=en:peutz-jeghers syndrome | n2=en:intestinal malrotation | rel=r_associated | relid=0 | w=30
  64. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:intraductal papillary mucinous neoplasm
    n1=en:peutz-jeghers syndrome | n2=en:intraductal papillary mucinous neoplasm | rel=r_associated | relid=0 | w=30
  65. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:laurin-sandrow syndrome
    n1=en:peutz-jeghers syndrome | n2=en:laurin-sandrow syndrome | rel=r_associated | relid=0 | w=30
  66. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:lynch syndrome
    n1=en:peutz-jeghers syndrome | n2=en:lynch syndrome | rel=r_associated | relid=0 | w=30
  67. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:macdermot winter syndrome
    n1=en:peutz-jeghers syndrome | n2=en:macdermot winter syndrome | rel=r_associated | relid=0 | w=30
  68. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:melnick-fraser syndrome
    n1=en:peutz-jeghers syndrome | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=30
  69. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis
    n1=en:peutz-jeghers syndrome | n2=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | rel=r_associated | relid=0 | w=30
  70. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:mohr-tranebjaerg syndrome
    n1=en:peutz-jeghers syndrome | n2=en:mohr-tranebjaerg syndrome | rel=r_associated | relid=0 | w=30
  71. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:mowat-wilson syndrome
    n1=en:peutz-jeghers syndrome | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=30
  72. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:myopathy, distal, tateyama type
    n1=en:peutz-jeghers syndrome | n2=en:myopathy, distal, tateyama type | rel=r_associated | relid=0 | w=30
  73. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:naxos disease
    n1=en:peutz-jeghers syndrome | n2=en:naxos disease | rel=r_associated | relid=0 | w=30
  74. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:neurofibromatosis
    n1=en:peutz-jeghers syndrome | n2=en:neurofibromatosis | rel=r_associated | relid=0 | w=30
  75. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:non-polyposis turcot syndrome
    n1=en:peutz-jeghers syndrome | n2=en:non-polyposis turcot syndrome | rel=r_associated | relid=0 | w=30
  76. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:papillon-lefevre syndrome
    n1=en:peutz-jeghers syndrome | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=30
  77. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:partington x-linked mental retardation syndrome
    n1=en:peutz-jeghers syndrome | n2=en:partington x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=30
  78. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:poikilodermatomyositis
    n1=en:peutz-jeghers syndrome | n2=en:poikilodermatomyositis | rel=r_associated | relid=0 | w=30
  79. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:polydactyly, preaxial ii (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:polydactyly, preaxial ii (disorder) | rel=r_associated | relid=0 | w=30
  80. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:polypoid sinus degeneration
    n1=en:peutz-jeghers syndrome | n2=en:polypoid sinus degeneration | rel=r_associated | relid=0 | w=30
  81. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:psychology qualifier
    n1=en:peutz-jeghers syndrome | n2=en:psychology qualifier | rel=r_associated | relid=0 | w=30
  82. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:radial hypoplasia, triphalangeal thumbs and hypospadias
    n1=en:peutz-jeghers syndrome | n2=en:radial hypoplasia, triphalangeal thumbs and hypospadias | rel=r_associated | relid=0 | w=30
  83. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:roentgenographic
    n1=en:peutz-jeghers syndrome | n2=en:roentgenographic | rel=r_associated | relid=0 | w=30
  84. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:skin discoloration
    n1=en:peutz-jeghers syndrome | n2=en:skin discoloration | rel=r_associated | relid=0 | w=30
  85. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:sotos syndrome
    n1=en:peutz-jeghers syndrome | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=30
  86. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:spinocerebellar ataxia 31 (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:spinocerebellar ataxia 31 (disorder) | rel=r_associated | relid=0 | w=30
  87. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:split-hand-foot malformation with long bone deficiency 1
    n1=en:peutz-jeghers syndrome | n2=en:split-hand-foot malformation with long bone deficiency 1 | rel=r_associated | relid=0 | w=30
  88. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:ulna metaphyseal dysplasia syndrome
    n1=en:peutz-jeghers syndrome | n2=en:ulna metaphyseal dysplasia syndrome | rel=r_associated | relid=0 | w=30
  89. en:peutz-jeghers syndrome -- r_associated #0: 30 / 0.577 -> en:ulnar-mammary syndrome
    n1=en:peutz-jeghers syndrome | n2=en:ulnar-mammary syndrome | rel=r_associated | relid=0 | w=30
  90. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> atrophie du foie
    n1=en:peutz-jeghers syndrome | n2=atrophie du foie | rel=r_associated | relid=0 | w=29
  91. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:abdominal wall neoplasm benign
    n1=en:peutz-jeghers syndrome | n2=en:abdominal wall neoplasm benign | rel=r_associated | relid=0 | w=29
  92. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:advanced sleep-phase syndrome, familial
    n1=en:peutz-jeghers syndrome | n2=en:advanced sleep-phase syndrome, familial | rel=r_associated | relid=0 | w=29
  93. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:allan-herndon-dudley syndrome
    n1=en:peutz-jeghers syndrome | n2=en:allan-herndon-dudley syndrome | rel=r_associated | relid=0 | w=29
  94. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:arthrogryposis, distal, type 1
    n1=en:peutz-jeghers syndrome | n2=en:arthrogryposis, distal, type 1 | rel=r_associated | relid=0 | w=29
  95. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:atrophy
    n1=en:peutz-jeghers syndrome | n2=en:atrophy | rel=r_associated | relid=0 | w=29
  96. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:benign colorectal neoplasm
    n1=en:peutz-jeghers syndrome | n2=en:benign colorectal neoplasm | rel=r_associated | relid=0 | w=29
  97. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
    n1=en:peutz-jeghers syndrome | n2=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | rel=r_associated | relid=0 | w=29
  98. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:charcot-marie-tooth disease, axonal, type 2e (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | rel=r_associated | relid=0 | w=29
  99. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:cleft lip/palate-ectodermal dysplasia syndrome
    n1=en:peutz-jeghers syndrome | n2=en:cleft lip/palate-ectodermal dysplasia syndrome | rel=r_associated | relid=0 | w=29
  100. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:cole disease
    n1=en:peutz-jeghers syndrome | n2=en:cole disease | rel=r_associated | relid=0 | w=29
  101. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:congenital anomaly of esophagus
    n1=en:peutz-jeghers syndrome | n2=en:congenital anomaly of esophagus | rel=r_associated | relid=0 | w=29
  102. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:crouzon syndrome with acanthosis nigricans (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29
  103. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:deafness-craniofacial syndrome
    n1=en:peutz-jeghers syndrome | n2=en:deafness-craniofacial syndrome | rel=r_associated | relid=0 | w=29
  104. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:dysplasia, saddan
    n1=en:peutz-jeghers syndrome | n2=en:dysplasia, saddan | rel=r_associated | relid=0 | w=29
  105. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:folinic acid responsive seizure syndrome
    n1=en:peutz-jeghers syndrome | n2=en:folinic acid responsive seizure syndrome | rel=r_associated | relid=0 | w=29
  106. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:gerstmann-straussler-scheinker disease
    n1=en:peutz-jeghers syndrome | n2=en:gerstmann-straussler-scheinker disease | rel=r_associated | relid=0 | w=29
  107. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:glycogen storage disease, hepatic form
    n1=en:peutz-jeghers syndrome | n2=en:glycogen storage disease, hepatic form | rel=r_associated | relid=0 | w=29
  108. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:haspeslagh fryns muelenaere syndrome
    n1=en:peutz-jeghers syndrome | n2=en:haspeslagh fryns muelenaere syndrome | rel=r_associated | relid=0 | w=29
  109. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:hereditary angioedema
    n1=en:peutz-jeghers syndrome | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=29
  110. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:hereditary cerebellar degeneration
    n1=en:peutz-jeghers syndrome | n2=en:hereditary cerebellar degeneration | rel=r_associated | relid=0 | w=29
  111. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:hereditary cerebral amyloid angiopathy, icelandic type
    n1=en:peutz-jeghers syndrome | n2=en:hereditary cerebral amyloid angiopathy, icelandic type | rel=r_associated | relid=0 | w=29
  112. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:hereditary non-polyposis colorectal cancer syndrome
    n1=en:peutz-jeghers syndrome | n2=en:hereditary non-polyposis colorectal cancer syndrome | rel=r_associated | relid=0 | w=29
  113. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:hyperferritinemia, hereditary, with congenital cataracts
    n1=en:peutz-jeghers syndrome | n2=en:hyperferritinemia, hereditary, with congenital cataracts | rel=r_associated | relid=0 | w=29
  114. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:hyperinsulinism due to deficiency of glucokinase
    n1=en:peutz-jeghers syndrome | n2=en:hyperinsulinism due to deficiency of glucokinase | rel=r_associated | relid=0 | w=29
  115. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:hypermelanosis due to hodgkin's disease
    n1=en:peutz-jeghers syndrome | n2=en:hypermelanosis due to hodgkin's disease | rel=r_associated | relid=0 | w=29
  116. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:inherited cutaneous hyperpigmentation
    n1=en:peutz-jeghers syndrome | n2=en:inherited cutaneous hyperpigmentation | rel=r_associated | relid=0 | w=29
  117. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:keratoacanthoma familial
    n1=en:peutz-jeghers syndrome | n2=en:keratoacanthoma familial | rel=r_associated | relid=0 | w=29
  118. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:lentigo - freckle
    n1=en:peutz-jeghers syndrome | n2=en:lentigo - freckle | rel=r_associated | relid=0 | w=29
  119. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:multiple endocrine neoplasia type 2b
    n1=en:peutz-jeghers syndrome | n2=en:multiple endocrine neoplasia type 2b | rel=r_associated | relid=0 | w=29
  120. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:multiple gastrointestinal atresias (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:multiple gastrointestinal atresias (disorder) | rel=r_associated | relid=0 | w=29
  121. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:nemaline myopathy 3
    n1=en:peutz-jeghers syndrome | n2=en:nemaline myopathy 3 | rel=r_associated | relid=0 | w=29
  122. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:neuropathy, hereditary motor and sensory, okinawa type
    n1=en:peutz-jeghers syndrome | n2=en:neuropathy, hereditary motor and sensory, okinawa type | rel=r_associated | relid=0 | w=29
  123. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:nicolaides baraitser syndrome
    n1=en:peutz-jeghers syndrome | n2=en:nicolaides baraitser syndrome | rel=r_associated | relid=0 | w=29
  124. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:oculocerebral hypopigmentation syndrome type preus
    n1=en:peutz-jeghers syndrome | n2=en:oculocerebral hypopigmentation syndrome type preus | rel=r_associated | relid=0 | w=29
  125. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:perniola krajewska carnevale syndrome
    n1=en:peutz-jeghers syndrome | n2=en:perniola krajewska carnevale syndrome | rel=r_associated | relid=0 | w=29
  126. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:pigmentation changes nec
    n1=en:peutz-jeghers syndrome | n2=en:pigmentation changes nec | rel=r_associated | relid=0 | w=29
  127. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:rhabdomyolysis
    n1=en:peutz-jeghers syndrome | n2=en:rhabdomyolysis | rel=r_associated | relid=0 | w=29
  128. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:shprintzen omphalocele syndrome
    n1=en:peutz-jeghers syndrome | n2=en:shprintzen omphalocele syndrome | rel=r_associated | relid=0 | w=29
  129. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:sitosterolemia with xanthomatosis
    n1=en:peutz-jeghers syndrome | n2=en:sitosterolemia with xanthomatosis | rel=r_associated | relid=0 | w=29
  130. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:spinocerebellar ataxia 36
    n1=en:peutz-jeghers syndrome | n2=en:spinocerebellar ataxia 36 | rel=r_associated | relid=0 | w=29
  131. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:spinocerebellar ataxia type 4
    n1=en:peutz-jeghers syndrome | n2=en:spinocerebellar ataxia type 4 | rel=r_associated | relid=0 | w=29
  132. en:peutz-jeghers syndrome -- r_associated #0: 29 / 0.558 -> en:strudwick syndrome
    n1=en:peutz-jeghers syndrome | n2=en:strudwick syndrome | rel=r_associated | relid=0 | w=29
  133. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:anterior displaced anus
    n1=en:peutz-jeghers syndrome | n2=en:anterior displaced anus | rel=r_associated | relid=0 | w=28
  134. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:beare-stevenson cutis gyrata syndrome
    n1=en:peutz-jeghers syndrome | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=28
  135. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:benign lymphoid polyposis of intestine
    n1=en:peutz-jeghers syndrome | n2=en:benign lymphoid polyposis of intestine | rel=r_associated | relid=0 | w=28
  136. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:cerebral cavernous malformation
    n1=en:peutz-jeghers syndrome | n2=en:cerebral cavernous malformation | rel=r_associated | relid=0 | w=28
  137. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:congenital anomaly of intestinal tract
    n1=en:peutz-jeghers syndrome | n2=en:congenital anomaly of intestinal tract | rel=r_associated | relid=0 | w=28
  138. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration
    n1=en:peutz-jeghers syndrome | n2=en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration | rel=r_associated | relid=0 | w=28
  139. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:congenital gastrointestinal-urinary tract fistula
    n1=en:peutz-jeghers syndrome | n2=en:congenital gastrointestinal-urinary tract fistula | rel=r_associated | relid=0 | w=28
  140. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:congenital sucrase-isomaltase deficiency
    n1=en:peutz-jeghers syndrome | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=28
  141. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:digestive system adenoma
    n1=en:peutz-jeghers syndrome | n2=en:digestive system adenoma | rel=r_associated | relid=0 | w=28
  142. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:duodenal atresia
    n1=en:peutz-jeghers syndrome | n2=en:duodenal atresia | rel=r_associated | relid=0 | w=28
  143. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:enteric duplication
    n1=en:peutz-jeghers syndrome | n2=en:enteric duplication | rel=r_associated | relid=0 | w=28
  144. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:enzymology
    n1=en:peutz-jeghers syndrome | n2=en:enzymology | rel=r_associated | relid=0 | w=28
  145. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:epidermolysis bullosa simplex with pyloric atresia
    n1=en:peutz-jeghers syndrome | n2=en:epidermolysis bullosa simplex with pyloric atresia | rel=r_associated | relid=0 | w=28
  146. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:eyelash hyperpigmentation
    n1=en:peutz-jeghers syndrome | n2=en:eyelash hyperpigmentation | rel=r_associated | relid=0 | w=28
  147. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:familial amyloid polyneuropathy with cutaneous amyloidosis
    n1=en:peutz-jeghers syndrome | n2=en:familial amyloid polyneuropathy with cutaneous amyloidosis | rel=r_associated | relid=0 | w=28
  148. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:familial digital arthropathy and brachydactyly syndrome
    n1=en:peutz-jeghers syndrome | n2=en:familial digital arthropathy and brachydactyly syndrome | rel=r_associated | relid=0 | w=28
  149. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:hand foot uterus syndrome
    n1=en:peutz-jeghers syndrome | n2=en:hand foot uterus syndrome | rel=r_associated | relid=0 | w=28
  150. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:hnsha due to triosephosphate isomerase deficiency
    n1=en:peutz-jeghers syndrome | n2=en:hnsha due to triosephosphate isomerase deficiency | rel=r_associated | relid=0 | w=28
  151. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:holoprosencephaly with fetal akinesia-hypokinesia sequence
    n1=en:peutz-jeghers syndrome | n2=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | rel=r_associated | relid=0 | w=28
  152. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:hydrocephalus with cerebellar agenesis
    n1=en:peutz-jeghers syndrome | n2=en:hydrocephalus with cerebellar agenesis | rel=r_associated | relid=0 | w=28
  153. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:hyperinsulinism due to hnf4a deficiency
    n1=en:peutz-jeghers syndrome | n2=en:hyperinsulinism due to hnf4a deficiency | rel=r_associated | relid=0 | w=28
  154. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:hyperpigmentation, familial progressive
    n1=en:peutz-jeghers syndrome | n2=en:hyperpigmentation, familial progressive | rel=r_associated | relid=0 | w=28
  155. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:hypotrichosis simplex of scalp
    n1=en:peutz-jeghers syndrome | n2=en:hypotrichosis simplex of scalp | rel=r_associated | relid=0 | w=28
  156. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:idiopathic lenticular mucocutaneous pigmentation
    n1=en:peutz-jeghers syndrome | n2=en:idiopathic lenticular mucocutaneous pigmentation | rel=r_associated | relid=0 | w=28
  157. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:imperforate anus
    n1=en:peutz-jeghers syndrome | n2=en:imperforate anus | rel=r_associated | relid=0 | w=28
  158. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:iron-deficiency anemia
    n1=en:peutz-jeghers syndrome | n2=en:iron-deficiency anemia | rel=r_associated | relid=0 | w=28
  159. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:kbg syndrome
    n1=en:peutz-jeghers syndrome | n2=en:kbg syndrome | rel=r_associated | relid=0 | w=28
  160. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:lamellar ichthyosis, autosomal dominant form
    n1=en:peutz-jeghers syndrome | n2=en:lamellar ichthyosis, autosomal dominant form | rel=r_associated | relid=0 | w=28
  161. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:lung
    n1=en:peutz-jeghers syndrome | n2=en:lung | rel=r_associated | relid=0 | w=28
  162. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:marfan syndrome
    n1=en:peutz-jeghers syndrome | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=28
  163. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:maternally inherited mitochondrial dystonia
    n1=en:peutz-jeghers syndrome | n2=en:maternally inherited mitochondrial dystonia | rel=r_associated | relid=0 | w=28
  164. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:microcephalic primordial dwarfism toriello type
    n1=en:peutz-jeghers syndrome | n2=en:microcephalic primordial dwarfism toriello type | rel=r_associated | relid=0 | w=28
  165. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:multiple endocrine neoplasia type 2a
    n1=en:peutz-jeghers syndrome | n2=en:multiple endocrine neoplasia type 2a | rel=r_associated | relid=0 | w=28
  166. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:oculodental syndrome rutherfurd syndrome
    n1=en:peutz-jeghers syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28
  167. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:pancreatic triacylglycerol lipase deficiency
    n1=en:peutz-jeghers syndrome | n2=en:pancreatic triacylglycerol lipase deficiency | rel=r_associated | relid=0 | w=28
  168. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:paroxysmal extreme pain disorder
    n1=en:peutz-jeghers syndrome | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=28
  169. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:peripheral resistance to thyroid hormone
    n1=en:peutz-jeghers syndrome | n2=en:peripheral resistance to thyroid hormone | rel=r_associated | relid=0 | w=28
  170. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:periventricular heterotopia, x-linked
    n1=en:peutz-jeghers syndrome | n2=en:periventricular heterotopia, x-linked | rel=r_associated | relid=0 | w=28
  171. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:poikiloderma of civatte
    n1=en:peutz-jeghers syndrome | n2=en:poikiloderma of civatte | rel=r_associated | relid=0 | w=28
  172. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:pseudocholinesterase deficiency
    n1=en:peutz-jeghers syndrome | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=28
  173. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:schindler disease, type i
    n1=en:peutz-jeghers syndrome | n2=en:schindler disease, type i | rel=r_associated | relid=0 | w=28
  174. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:spinocerebellar ataxia type 2
    n1=en:peutz-jeghers syndrome | n2=en:spinocerebellar ataxia type 2 | rel=r_associated | relid=0 | w=28
  175. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:steatohepatitis
    n1=en:peutz-jeghers syndrome | n2=en:steatohepatitis | rel=r_associated | relid=0 | w=28
  176. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:stoma site polyp
    n1=en:peutz-jeghers syndrome | n2=en:stoma site polyp | rel=r_associated | relid=0 | w=28
  177. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:syndactyly, type iii
    n1=en:peutz-jeghers syndrome | n2=en:syndactyly, type iii | rel=r_associated | relid=0 | w=28
  178. en:peutz-jeghers syndrome -- r_associated #0: 28 / 0.538 -> en:wells jankovic syndrome
    n1=en:peutz-jeghers syndrome | n2=en:wells jankovic syndrome | rel=r_associated | relid=0 | w=28
  179. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> anomalie congénitale
    n1=en:peutz-jeghers syndrome | n2=anomalie congénitale | rel=r_associated | relid=0 | w=27
  180. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:acquired lentiginosis
    n1=en:peutz-jeghers syndrome | n2=en:acquired lentiginosis | rel=r_associated | relid=0 | w=27
  181. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:acrodermatitis enteropathica
    n1=en:peutz-jeghers syndrome | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=27
  182. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:arsenic-induced skin pigmentation
    n1=en:peutz-jeghers syndrome | n2=en:arsenic-induced skin pigmentation | rel=r_associated | relid=0 | w=27
  183. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:aspects of mortality statistics
    n1=en:peutz-jeghers syndrome | n2=en:aspects of mortality statistics | rel=r_associated | relid=0 | w=27
  184. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:ataxia telangiectasia syndrome
    n1=en:peutz-jeghers syndrome | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=27
  185. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:ataxia with vitamin e deficiency
    n1=en:peutz-jeghers syndrome | n2=en:ataxia with vitamin e deficiency | rel=r_associated | relid=0 | w=27
  186. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:atrophy of vagina
    n1=en:peutz-jeghers syndrome | n2=en:atrophy of vagina | rel=r_associated | relid=0 | w=27
  187. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:autosomal dominant optic atrophy
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant optic atrophy | rel=r_associated | relid=0 | w=27
  188. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:benign digestive system neoplasm
    n1=en:peutz-jeghers syndrome | n2=en:benign digestive system neoplasm | rel=r_associated | relid=0 | w=27
  189. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:bituminosis
    n1=en:peutz-jeghers syndrome | n2=en:bituminosis | rel=r_associated | relid=0 | w=27
  190. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:brachyolmia type 3
    n1=en:peutz-jeghers syndrome | n2=en:brachyolmia type 3 | rel=r_associated | relid=0 | w=27
  191. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:char syndrome
    n1=en:peutz-jeghers syndrome | n2=en:char syndrome | rel=r_associated | relid=0 | w=27
  192. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:cleidocranial dysplasia
    n1=en:peutz-jeghers syndrome | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=27
  193. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:cobb syndrome
    n1=en:peutz-jeghers syndrome | n2=en:cobb syndrome | rel=r_associated | relid=0 | w=27
  194. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:congenital abnormality
    n1=en:peutz-jeghers syndrome | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=27
  195. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:congenital cataracts, facial dysmorphism, and neuropathy
    n1=en:peutz-jeghers syndrome | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=27
  196. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:congenital duplication of appendix
    n1=en:peutz-jeghers syndrome | n2=en:congenital duplication of appendix | rel=r_associated | relid=0 | w=27
  197. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:congenital nephrogenic diabetes insipidus
    n1=en:peutz-jeghers syndrome | n2=en:congenital nephrogenic diabetes insipidus | rel=r_associated | relid=0 | w=27
  198. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:dystonia 12
    n1=en:peutz-jeghers syndrome | n2=en:dystonia 12 | rel=r_associated | relid=0 | w=27
  199. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:epiphyseal dysplasia, multiple, 1
    n1=en:peutz-jeghers syndrome | n2=en:epiphyseal dysplasia, multiple, 1 | rel=r_associated | relid=0 | w=27
  200. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:episodic ataxia
    n1=en:peutz-jeghers syndrome | n2=en:episodic ataxia | rel=r_associated | relid=0 | w=27
  201. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:etiology aspects
    n1=en:peutz-jeghers syndrome | n2=en:etiology aspects | rel=r_associated | relid=0 | w=27
  202. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:familial amyloid neuropathy
    n1=en:peutz-jeghers syndrome | n2=en:familial amyloid neuropathy | rel=r_associated | relid=0 | w=27
  203. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:familial osteochondritis dissecans
    n1=en:peutz-jeghers syndrome | n2=en:familial osteochondritis dissecans | rel=r_associated | relid=0 | w=27
  204. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:gingival odontogenic cyst
    n1=en:peutz-jeghers syndrome | n2=en:gingival odontogenic cyst | rel=r_associated | relid=0 | w=27
  205. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:glomuvenous malformations
    n1=en:peutz-jeghers syndrome | n2=en:glomuvenous malformations | rel=r_associated | relid=0 | w=27
  206. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:hereditary myopathy with early respiratory failure
    n1=en:peutz-jeghers syndrome | n2=en:hereditary myopathy with early respiratory failure | rel=r_associated | relid=0 | w=27
  207. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:hereditary peripheral neuropathy
    n1=en:peutz-jeghers syndrome | n2=en:hereditary peripheral neuropathy | rel=r_associated | relid=0 | w=27
  208. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:hereditary systemic amyloidosis
    n1=en:peutz-jeghers syndrome | n2=en:hereditary systemic amyloidosis | rel=r_associated | relid=0 | w=27
  209. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:hypoplastic tibia and postaxial polydactyly syndrome
    n1=en:peutz-jeghers syndrome | n2=en:hypoplastic tibia and postaxial polydactyly syndrome | rel=r_associated | relid=0 | w=27
  210. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:jackson-weiss syndrome
    n1=en:peutz-jeghers syndrome | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=27
  211. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:knobloch syndrome
    n1=en:peutz-jeghers syndrome | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=27
  212. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:lissencephaly syndrome, norman-roberts type
    n1=en:peutz-jeghers syndrome | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=27
  213. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:melanosis
    n1=en:peutz-jeghers syndrome | n2=en:melanosis | rel=r_associated | relid=0 | w=27
  214. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:melasma
    n1=en:peutz-jeghers syndrome | n2=en:melasma | rel=r_associated | relid=0 | w=27
  215. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:menkes disease
    n1=en:peutz-jeghers syndrome | n2=en:menkes disease | rel=r_associated | relid=0 | w=27
  216. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:mesomelic dwarfism reinhardt pfeiffer type
    n1=en:peutz-jeghers syndrome | n2=en:mesomelic dwarfism reinhardt pfeiffer type | rel=r_associated | relid=0 | w=27
  217. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:microbiological
    n1=en:peutz-jeghers syndrome | n2=en:microbiological | rel=r_associated | relid=0 | w=27
  218. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:mixed hypo- and hyperpigmentation of the skin
    n1=en:peutz-jeghers syndrome | n2=en:mixed hypo- and hyperpigmentation of the skin | rel=r_associated | relid=0 | w=27
  219. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:neuronal ceroid lipofuscinosis
    n1=en:peutz-jeghers syndrome | n2=en:neuronal ceroid lipofuscinosis | rel=r_associated | relid=0 | w=27
  220. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:osteolysis
    n1=en:peutz-jeghers syndrome | n2=en:osteolysis | rel=r_associated | relid=0 | w=27
  221. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:other congenital malformations of digestive system
    n1=en:peutz-jeghers syndrome | n2=en:other congenital malformations of digestive system | rel=r_associated | relid=0 | w=27
  222. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:porphyria
    n1=en:peutz-jeghers syndrome | n2=en:porphyria | rel=r_associated | relid=0 | w=27
  223. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:pseudoatrophoderma colli
    n1=en:peutz-jeghers syndrome | n2=en:pseudoatrophoderma colli | rel=r_associated | relid=0 | w=27
  224. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:retroperitoneal cyst
    n1=en:peutz-jeghers syndrome | n2=en:retroperitoneal cyst | rel=r_associated | relid=0 | w=27
  225. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:spinocerebellar ataxia type 6 (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:spinocerebellar ataxia type 6 (disorder) | rel=r_associated | relid=0 | w=27
  226. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:syndrome, branchio-oculo-facial
    n1=en:peutz-jeghers syndrome | n2=en:syndrome, branchio-oculo-facial | rel=r_associated | relid=0 | w=27
  227. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:transposition of intestine (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:transposition of intestine (disorder) | rel=r_associated | relid=0 | w=27
  228. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:treacher collins syndrome
    n1=en:peutz-jeghers syndrome | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=27
  229. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:trichohepatoenteric syndrome
    n1=en:peutz-jeghers syndrome | n2=en:trichohepatoenteric syndrome | rel=r_associated | relid=0 | w=27
  230. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:tuberous sclerosis
    n1=en:peutz-jeghers syndrome | n2=en:tuberous sclerosis | rel=r_associated | relid=0 | w=27
  231. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:vitelliform macular dystrophy
    n1=en:peutz-jeghers syndrome | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=27
  232. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:vitreoretinochoroidopathy (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:vitreoretinochoroidopathy (disorder) | rel=r_associated | relid=0 | w=27
  233. en:peutz-jeghers syndrome -- r_associated #0: 27 / 0.519 -> en:wellesley carman french syndrome
    n1=en:peutz-jeghers syndrome | n2=en:wellesley carman french syndrome | rel=r_associated | relid=0 | w=27
  234. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> atrophie hépatique
    n1=en:peutz-jeghers syndrome | n2=atrophie hépatique | rel=r_associated | relid=0 | w=26
  235. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:2-hydroxyglutaric aciduria
    n1=en:peutz-jeghers syndrome | n2=en:2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=26
  236. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:acromicric dysplasia
    n1=en:peutz-jeghers syndrome | n2=en:acromicric dysplasia | rel=r_associated | relid=0 | w=26
  237. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:allgrove syndrome
    n1=en:peutz-jeghers syndrome | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=26
  238. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:alpha-fetoprotein, hereditary persistence of
    n1=en:peutz-jeghers syndrome | n2=en:alpha-fetoprotein, hereditary persistence of | rel=r_associated | relid=0 | w=26
  239. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:alpha-methylacyl-coa racemase deficiency
    n1=en:peutz-jeghers syndrome | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=26
  240. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:aspects of radionuclide imaging
    n1=en:peutz-jeghers syndrome | n2=en:aspects of radionuclide imaging | rel=r_associated | relid=0 | w=26
  241. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:autosomal dominant muscular dystrophy not predominantly limb girdle
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant muscular dystrophy not predominantly limb girdle | rel=r_associated | relid=0 | w=26
  242. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:autosomal dominant progressive nephropathy with hypertension
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant progressive nephropathy with hypertension | rel=r_associated | relid=0 | w=26
  243. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:autosomal recessive primary microcephaly
    n1=en:peutz-jeghers syndrome | n2=en:autosomal recessive primary microcephaly | rel=r_associated | relid=0 | w=26
  244. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:bilateral multiple fibroadenoma of breast
    n1=en:peutz-jeghers syndrome | n2=en:bilateral multiple fibroadenoma of breast | rel=r_associated | relid=0 | w=26
  245. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:brooke-spiegler syndrome
    n1=en:peutz-jeghers syndrome | n2=en:brooke-spiegler syndrome | rel=r_associated | relid=0 | w=26
  246. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:cerebrotendinous xanthomatosis
    n1=en:peutz-jeghers syndrome | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=26
  247. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism
    n1=en:peutz-jeghers syndrome | n2=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=26
  248. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:chromosome 3q29 deletion syndrome
    n1=en:peutz-jeghers syndrome | n2=en:chromosome 3q29 deletion syndrome | rel=r_associated | relid=0 | w=26
  249. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:congenital malformation of upper alimentary tract
    n1=en:peutz-jeghers syndrome | n2=en:congenital malformation of upper alimentary tract | rel=r_associated | relid=0 | w=26
  250. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:degenerative disorder of head
    n1=en:peutz-jeghers syndrome | n2=en:degenerative disorder of head | rel=r_associated | relid=0 | w=26
  251. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:dopa-responsive dystonia
    n1=en:peutz-jeghers syndrome | n2=en:dopa-responsive dystonia | rel=r_associated | relid=0 | w=26
  252. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:enterokinase deficiency
    n1=en:peutz-jeghers syndrome | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=26
  253. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:epilepsy, myoclonic, benign adult familial, type 2
    n1=en:peutz-jeghers syndrome | n2=en:epilepsy, myoclonic, benign adult familial, type 2 | rel=r_associated | relid=0 | w=26
  254. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:familial hemiplegic migraine
    n1=en:peutz-jeghers syndrome | n2=en:familial hemiplegic migraine | rel=r_associated | relid=0 | w=26
  255. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:familial partial lipodystrophy, type 2
    n1=en:peutz-jeghers syndrome | n2=en:familial partial lipodystrophy, type 2 | rel=r_associated | relid=0 | w=26
  256. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:hemiatrophy of lower limb
    n1=en:peutz-jeghers syndrome | n2=en:hemiatrophy of lower limb | rel=r_associated | relid=0 | w=26
  257. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:hereditary diffuse gastric adenocarcinoma
    n1=en:peutz-jeghers syndrome | n2=en:hereditary diffuse gastric adenocarcinoma | rel=r_associated | relid=0 | w=26
  258. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:hereditary multiple exostoses
    n1=en:peutz-jeghers syndrome | n2=en:hereditary multiple exostoses | rel=r_associated | relid=0 | w=26
  259. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:hereditary papillary renal cell carcinoma
    n1=en:peutz-jeghers syndrome | n2=en:hereditary papillary renal cell carcinoma | rel=r_associated | relid=0 | w=26
  260. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia
    n1=en:peutz-jeghers syndrome | n2=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | rel=r_associated | relid=0 | w=26
  261. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:intestinal cyst
    n1=en:peutz-jeghers syndrome | n2=en:intestinal cyst | rel=r_associated | relid=0 | w=26
  262. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies
    n1=en:peutz-jeghers syndrome | n2=en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies | rel=r_associated | relid=0 | w=26
  263. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:labial lentigo
    n1=en:peutz-jeghers syndrome | n2=en:labial lentigo | rel=r_associated | relid=0 | w=26
  264. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:large intestine atresia
    n1=en:peutz-jeghers syndrome | n2=en:large intestine atresia | rel=r_associated | relid=0 | w=26
  265. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:leigh disease
    n1=en:peutz-jeghers syndrome | n2=en:leigh disease | rel=r_associated | relid=0 | w=26
  266. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:leopard syndrome
    n1=en:peutz-jeghers syndrome | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=26
  267. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:microcolon
    n1=en:peutz-jeghers syndrome | n2=en:microcolon | rel=r_associated | relid=0 | w=26
  268. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:microphthalmia, syndromic 3
    n1=en:peutz-jeghers syndrome | n2=en:microphthalmia, syndromic 3 | rel=r_associated | relid=0 | w=26
  269. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:neurofibromatosis type 2
    n1=en:peutz-jeghers syndrome | n2=en:neurofibromatosis type 2 | rel=r_associated | relid=0 | w=26
  270. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:noonan syndrome
    n1=en:peutz-jeghers syndrome | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=26
  271. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:persistent cloaca
    n1=en:peutz-jeghers syndrome | n2=en:persistent cloaca | rel=r_associated | relid=0 | w=26
  272. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:piebaldism
    n1=en:peutz-jeghers syndrome | n2=en:piebaldism | rel=r_associated | relid=0 | w=26
  273. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:pili torti-deafness syndrome
    n1=en:peutz-jeghers syndrome | n2=en:pili torti-deafness syndrome | rel=r_associated | relid=0 | w=26
  274. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:potassium aggravated myotonia
    n1=en:peutz-jeghers syndrome | n2=en:potassium aggravated myotonia | rel=r_associated | relid=0 | w=26
  275. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:premature aging syndrome
    n1=en:peutz-jeghers syndrome | n2=en:premature aging syndrome | rel=r_associated | relid=0 | w=26
  276. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:pseudohypoaldosteronism, type 1, dominant form
    n1=en:peutz-jeghers syndrome | n2=en:pseudohypoaldosteronism, type 1, dominant form | rel=r_associated | relid=0 | w=26
  277. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:rud syndrome
    n1=en:peutz-jeghers syndrome | n2=en:rud syndrome | rel=r_associated | relid=0 | w=26
  278. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:steinfeld syndrome
    n1=en:peutz-jeghers syndrome | n2=en:steinfeld syndrome | rel=r_associated | relid=0 | w=26
  279. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:vacterl association
    n1=en:peutz-jeghers syndrome | n2=en:vacterl association | rel=r_associated | relid=0 | w=26
  280. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:von hippel-lindau syndrome
    n1=en:peutz-jeghers syndrome | n2=en:von hippel-lindau syndrome | rel=r_associated | relid=0 | w=26
  281. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> en:waisman syndrome
    n1=en:peutz-jeghers syndrome | n2=en:waisman syndrome | rel=r_associated | relid=0 | w=26
  282. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> syndrome de Marfan
    n1=en:peutz-jeghers syndrome | n2=syndrome de Marfan | rel=r_associated | relid=0 | w=26
  283. en:peutz-jeghers syndrome -- r_associated #0: 26 / 0.5 -> syndrome de Walker-Warburg
    n1=en:peutz-jeghers syndrome | n2=syndrome de Walker-Warburg | rel=r_associated | relid=0 | w=26
  284. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:aicardi syndrome
    n1=en:peutz-jeghers syndrome | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=25
  285. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:alagille syndrome
    n1=en:peutz-jeghers syndrome | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=25
  286. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:angiokeratoma corporis diffusum
    n1=en:peutz-jeghers syndrome | n2=en:angiokeratoma corporis diffusum | rel=r_associated | relid=0 | w=25
  287. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:anorectal agenesis
    n1=en:peutz-jeghers syndrome | n2=en:anorectal agenesis | rel=r_associated | relid=0 | w=25
  288. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:atrophy of pancreas
    n1=en:peutz-jeghers syndrome | n2=en:atrophy of pancreas | rel=r_associated | relid=0 | w=25
  289. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:avascular necrosis of femoral head
    n1=en:peutz-jeghers syndrome | n2=en:avascular necrosis of femoral head | rel=r_associated | relid=0 | w=25
  290. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:brachymesophalangy 2 and 5
    n1=en:peutz-jeghers syndrome | n2=en:brachymesophalangy 2 and 5 | rel=r_associated | relid=0 | w=25
  291. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:cerebral hemorrhage with amyloidosis, hereditary, dutch type
    n1=en:peutz-jeghers syndrome | n2=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | rel=r_associated | relid=0 | w=25
  292. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:corneal dystrophy, congenital stromal
    n1=en:peutz-jeghers syndrome | n2=en:corneal dystrophy, congenital stromal | rel=r_associated | relid=0 | w=25
  293. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:cutis laxa, autosomal recessive
    n1=en:peutz-jeghers syndrome | n2=en:cutis laxa, autosomal recessive | rel=r_associated | relid=0 | w=25
  294. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:diabetic truncal radiculopathy
    n1=en:peutz-jeghers syndrome | n2=en:diabetic truncal radiculopathy | rel=r_associated | relid=0 | w=25
  295. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:familial non-autoimmune autosomal dominant hyperthyroidism
    n1=en:peutz-jeghers syndrome | n2=en:familial non-autoimmune autosomal dominant hyperthyroidism | rel=r_associated | relid=0 | w=25
  296. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:gaze palsy, familial horizontal, with progressive scoliosis
    n1=en:peutz-jeghers syndrome | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=25
  297. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:generalized epilepsy and paroxysmal dyskinesia syndrome
    n1=en:peutz-jeghers syndrome | n2=en:generalized epilepsy and paroxysmal dyskinesia syndrome | rel=r_associated | relid=0 | w=25
  298. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:glycogen storage disease 0, liver
    n1=en:peutz-jeghers syndrome | n2=en:glycogen storage disease 0, liver | rel=r_associated | relid=0 | w=25
  299. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:hereditary optic atrophy
    n1=en:peutz-jeghers syndrome | n2=en:hereditary optic atrophy | rel=r_associated | relid=0 | w=25
  300. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:hypomagnesemia 1, intestinal
    n1=en:peutz-jeghers syndrome | n2=en:hypomagnesemia 1, intestinal | rel=r_associated | relid=0 | w=25
  301. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:hypomyelination and congenital cataract
    n1=en:peutz-jeghers syndrome | n2=en:hypomyelination and congenital cataract | rel=r_associated | relid=0 | w=25
  302. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:intestinal disorders congenital
    n1=en:peutz-jeghers syndrome | n2=en:intestinal disorders congenital | rel=r_associated | relid=0 | w=25
  303. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:liddle syndrome
    n1=en:peutz-jeghers syndrome | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=25
  304. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:lowry yong syndrome
    n1=en:peutz-jeghers syndrome | n2=en:lowry yong syndrome | rel=r_associated | relid=0 | w=25
  305. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:macular pigment deposit
    n1=en:peutz-jeghers syndrome | n2=en:macular pigment deposit | rel=r_associated | relid=0 | w=25
  306. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:megalencephalic leukoencephalopathy with subcortical cysts
    n1=en:peutz-jeghers syndrome | n2=en:megalencephalic leukoencephalopathy with subcortical cysts | rel=r_associated | relid=0 | w=25
  307. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:microcornea with glaucoma and absent frontal sinus syndrome
    n1=en:peutz-jeghers syndrome | n2=en:microcornea with glaucoma and absent frontal sinus syndrome | rel=r_associated | relid=0 | w=25
  308. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:mobile caecum syndrome
    n1=en:peutz-jeghers syndrome | n2=en:mobile caecum syndrome | rel=r_associated | relid=0 | w=25
  309. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:multiple endocrine neoplasia type 1
    n1=en:peutz-jeghers syndrome | n2=en:multiple endocrine neoplasia type 1 | rel=r_associated | relid=0 | w=25
  310. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:mutyh-associated polyposis
    n1=en:peutz-jeghers syndrome | n2=en:mutyh-associated polyposis | rel=r_associated | relid=0 | w=25
  311. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:necrotic process
    n1=en:peutz-jeghers syndrome | n2=en:necrotic process | rel=r_associated | relid=0 | w=25
  312. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:neuronal intestinal dysplasia
    n1=en:peutz-jeghers syndrome | n2=en:neuronal intestinal dysplasia | rel=r_associated | relid=0 | w=25
  313. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:nevoid basal cell carcinoma syndrome
    n1=en:peutz-jeghers syndrome | n2=en:nevoid basal cell carcinoma syndrome | rel=r_associated | relid=0 | w=25
  314. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:panniculitis due to hyperuricemia
    n1=en:peutz-jeghers syndrome | n2=en:panniculitis due to hyperuricemia | rel=r_associated | relid=0 | w=25
  315. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:pituitary adenoma, familial isolated (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:pituitary adenoma, familial isolated (disorder) | rel=r_associated | relid=0 | w=25
  316. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:pontocerebellar hypoplasia type 2
    n1=en:peutz-jeghers syndrome | n2=en:pontocerebellar hypoplasia type 2 | rel=r_associated | relid=0 | w=25
  317. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:port wine stain
    n1=en:peutz-jeghers syndrome | n2=en:port wine stain | rel=r_associated | relid=0 | w=25
  318. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:proteus-like syndrome (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:proteus-like syndrome (disorder) | rel=r_associated | relid=0 | w=25
  319. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:roch leri mesosomatous lipomatosis
    n1=en:peutz-jeghers syndrome | n2=en:roch leri mesosomatous lipomatosis | rel=r_associated | relid=0 | w=25
  320. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
    n1=en:peutz-jeghers syndrome | n2=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | rel=r_associated | relid=0 | w=25
  321. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:spinocerebellar ataxia 29
    n1=en:peutz-jeghers syndrome | n2=en:spinocerebellar ataxia 29 | rel=r_associated | relid=0 | w=25
  322. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:syndactyly, type i
    n1=en:peutz-jeghers syndrome | n2=en:syndactyly, type i | rel=r_associated | relid=0 | w=25
  323. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:syndromic orbital border hypoplasia
    n1=en:peutz-jeghers syndrome | n2=en:syndromic orbital border hypoplasia | rel=r_associated | relid=0 | w=25
  324. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:tmem70 related mitochondrial encephalo-cardio-myopathy
    n1=en:peutz-jeghers syndrome | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=25
  325. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:turcot syndrome
    n1=en:peutz-jeghers syndrome | n2=en:turcot syndrome | rel=r_associated | relid=0 | w=25
  326. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:vitello-intestinal duct remnant
    n1=en:peutz-jeghers syndrome | n2=en:vitello-intestinal duct remnant | rel=r_associated | relid=0 | w=25
  327. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:wnt4 mullerian aplasia and ovarian dysfunction
    n1=en:peutz-jeghers syndrome | n2=en:wnt4 mullerian aplasia and ovarian dysfunction | rel=r_associated | relid=0 | w=25
  328. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> en:x-linked lissencephaly
    n1=en:peutz-jeghers syndrome | n2=en:x-linked lissencephaly | rel=r_associated | relid=0 | w=25
  329. en:peutz-jeghers syndrome -- r_associated #0: 25 / 0.481 -> poumon
    n1=en:peutz-jeghers syndrome | n2=poumon | rel=r_associated | relid=0 | w=25
  330. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:aase syndrome
    n1=en:peutz-jeghers syndrome | n2=en:aase syndrome | rel=r_associated | relid=0 | w=24
  331. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:ameloonychohypohidrotic syndrome
    n1=en:peutz-jeghers syndrome | n2=en:ameloonychohypohidrotic syndrome | rel=r_associated | relid=0 | w=24
  332. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:autosomal dominant charcot-marie-tooth disease type 2c
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant charcot-marie-tooth disease type 2c | rel=r_associated | relid=0 | w=24
  333. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:autosomal dominant deficiency of plasminogen
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant deficiency of plasminogen | rel=r_associated | relid=0 | w=24
  334. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:autosomal dominant idiopathic familial dystonia
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant idiopathic familial dystonia | rel=r_associated | relid=0 | w=24
  335. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:behr syndrome
    n1=en:peutz-jeghers syndrome | n2=en:behr syndrome | rel=r_associated | relid=0 | w=24
  336. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:capillary malformation-arteriovenous malformation (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:capillary malformation-arteriovenous malformation (disorder) | rel=r_associated | relid=0 | w=24
  337. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:cerebellar ataxia ectodermal dysplasia
    n1=en:peutz-jeghers syndrome | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=24
  338. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:cerebroretinal microangiopathy with calcifications and cysts (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | rel=r_associated | relid=0 | w=24
  339. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:congenital dyserythropoietic anemia, type iii
    n1=en:peutz-jeghers syndrome | n2=en:congenital dyserythropoietic anemia, type iii | rel=r_associated | relid=0 | w=24
  340. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:congenital intestinal obstruction
    n1=en:peutz-jeghers syndrome | n2=en:congenital intestinal obstruction | rel=r_associated | relid=0 | w=24
  341. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:congenital/hereditary lentiginosis
    n1=en:peutz-jeghers syndrome | n2=en:congenital/hereditary lentiginosis | rel=r_associated | relid=0 | w=24
  342. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:craniofacial deafness hand syndrome
    n1=en:peutz-jeghers syndrome | n2=en:craniofacial deafness hand syndrome | rel=r_associated | relid=0 | w=24
  343. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:crigler-najjar syndrome
    n1=en:peutz-jeghers syndrome | n2=en:crigler-najjar syndrome | rel=r_associated | relid=0 | w=24
  344. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:dentatorubral-pallidoluysian atrophy
    n1=en:peutz-jeghers syndrome | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=24
  345. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:disorder of central nervous system due to xeroderma pigmentosum
    n1=en:peutz-jeghers syndrome | n2=en:disorder of central nervous system due to xeroderma pigmentosum | rel=r_associated | relid=0 | w=24
  346. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:disseminated superficial porokeratosis
    n1=en:peutz-jeghers syndrome | n2=en:disseminated superficial porokeratosis | rel=r_associated | relid=0 | w=24
  347. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:dominant autosomal hereditary disorder, incomplete penetrance
    n1=en:peutz-jeghers syndrome | n2=en:dominant autosomal hereditary disorder, incomplete penetrance | rel=r_associated | relid=0 | w=24
  348. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:ectodermal dysplasia/ skin fragility syndrome
    n1=en:peutz-jeghers syndrome | n2=en:ectodermal dysplasia/ skin fragility syndrome | rel=r_associated | relid=0 | w=24
  349. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:encephalopathy due to sulfite oxidase deficiency
    n1=en:peutz-jeghers syndrome | n2=en:encephalopathy due to sulfite oxidase deficiency | rel=r_associated | relid=0 | w=24
  350. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:esophageal atresia
    n1=en:peutz-jeghers syndrome | n2=en:esophageal atresia | rel=r_associated | relid=0 | w=24
  351. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:familial chronic pancreatitis
    n1=en:peutz-jeghers syndrome | n2=en:familial chronic pancreatitis | rel=r_associated | relid=0 | w=24
  352. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:gastrointestinal vessel anomaly
    n1=en:peutz-jeghers syndrome | n2=en:gastrointestinal vessel anomaly | rel=r_associated | relid=0 | w=24
  353. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:hereditary cerebellar atrophy
    n1=en:peutz-jeghers syndrome | n2=en:hereditary cerebellar atrophy | rel=r_associated | relid=0 | w=24
  354. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:hereditary cystatin c amyloid angiopathy
    n1=en:peutz-jeghers syndrome | n2=en:hereditary cystatin c amyloid angiopathy | rel=r_associated | relid=0 | w=24
  355. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:hereditary gingival fibromatosis
    n1=en:peutz-jeghers syndrome | n2=en:hereditary gingival fibromatosis | rel=r_associated | relid=0 | w=24
  356. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:hereditary mucosal leukokeratosis
    n1=en:peutz-jeghers syndrome | n2=en:hereditary mucosal leukokeratosis | rel=r_associated | relid=0 | w=24
  357. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:keratosis palmoplantaris papulosa
    n1=en:peutz-jeghers syndrome | n2=en:keratosis palmoplantaris papulosa | rel=r_associated | relid=0 | w=24
  358. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:kidney wilms tumor
    n1=en:peutz-jeghers syndrome | n2=en:kidney wilms tumor | rel=r_associated | relid=0 | w=24
  359. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:lissencephaly, x-linked, 2
    n1=en:peutz-jeghers syndrome | n2=en:lissencephaly, x-linked, 2 | rel=r_associated | relid=0 | w=24
  360. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:metaplastic polyposis of intestine
    n1=en:peutz-jeghers syndrome | n2=en:metaplastic polyposis of intestine | rel=r_associated | relid=0 | w=24
  361. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:microcephaly cervical spine fusion anomalies
    n1=en:peutz-jeghers syndrome | n2=en:microcephaly cervical spine fusion anomalies | rel=r_associated | relid=0 | w=24
  362. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome
    n1=en:peutz-jeghers syndrome | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=24
  363. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:mousa al din al nassar syndrome
    n1=en:peutz-jeghers syndrome | n2=en:mousa al din al nassar syndrome | rel=r_associated | relid=0 | w=24
  364. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:muckle-wells syndrome
    n1=en:peutz-jeghers syndrome | n2=en:muckle-wells syndrome | rel=r_associated | relid=0 | w=24
  365. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:mucous patch of oral mucosa
    n1=en:peutz-jeghers syndrome | n2=en:mucous patch of oral mucosa | rel=r_associated | relid=0 | w=24
  366. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:myomalacia
    n1=en:peutz-jeghers syndrome | n2=en:myomalacia | rel=r_associated | relid=0 | w=24
  367. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:nance-horan syndrome
    n1=en:peutz-jeghers syndrome | n2=en:nance-horan syndrome | rel=r_associated | relid=0 | w=24
  368. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:neuropathy, hereditary thermosensitive
    n1=en:peutz-jeghers syndrome | n2=en:neuropathy, hereditary thermosensitive | rel=r_associated | relid=0 | w=24
  369. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:okihiro syndrome
    n1=en:peutz-jeghers syndrome | n2=en:okihiro syndrome | rel=r_associated | relid=0 | w=24
  370. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:otoonychoperoneal syndrome
    n1=en:peutz-jeghers syndrome | n2=en:otoonychoperoneal syndrome | rel=r_associated | relid=0 | w=24
  371. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:parasitology
    n1=en:peutz-jeghers syndrome | n2=en:parasitology | rel=r_associated | relid=0 | w=24
  372. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:pharmacotherapeutic
    n1=en:peutz-jeghers syndrome | n2=en:pharmacotherapeutic | rel=r_associated | relid=0 | w=24
  373. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:pituitary thyroid hormone resistance
    n1=en:peutz-jeghers syndrome | n2=en:pituitary thyroid hormone resistance | rel=r_associated | relid=0 | w=24
  374. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
    n1=en:peutz-jeghers syndrome | n2=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | rel=r_associated | relid=0 | w=24
  375. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:preternatural anus
    n1=en:peutz-jeghers syndrome | n2=en:preternatural anus | rel=r_associated | relid=0 | w=24
  376. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:reis-bucklers' corneal dystrophy
    n1=en:peutz-jeghers syndrome | n2=en:reis-bucklers' corneal dystrophy | rel=r_associated | relid=0 | w=24
  377. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:scleroderma-associated hypermelanosis
    n1=en:peutz-jeghers syndrome | n2=en:scleroderma-associated hypermelanosis | rel=r_associated | relid=0 | w=24
  378. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:sebastian syndrome
    n1=en:peutz-jeghers syndrome | n2=en:sebastian syndrome | rel=r_associated | relid=0 | w=24
  379. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:short stature with valvular heart disease and characteristic facies syndrome
    n1=en:peutz-jeghers syndrome | n2=en:short stature with valvular heart disease and characteristic facies syndrome | rel=r_associated | relid=0 | w=24
  380. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:simpson golabi behmel syndrome type 1
    n1=en:peutz-jeghers syndrome | n2=en:simpson golabi behmel syndrome type 1 | rel=r_associated | relid=0 | w=24
  381. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:spinocerebellar ataxia 1s
    n1=en:peutz-jeghers syndrome | n2=en:spinocerebellar ataxia 1s | rel=r_associated | relid=0 | w=24
  382. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:spinocerebellar ataxia type 5
    n1=en:peutz-jeghers syndrome | n2=en:spinocerebellar ataxia type 5 | rel=r_associated | relid=0 | w=24
  383. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:sting-associated vasculopathy with onset in infancy
    n1=en:peutz-jeghers syndrome | n2=en:sting-associated vasculopathy with onset in infancy | rel=r_associated | relid=0 | w=24
  384. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:synpolydactyly
    n1=en:peutz-jeghers syndrome | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=24
  385. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:therapeutic aspects
    n1=en:peutz-jeghers syndrome | n2=en:therapeutic aspects | rel=r_associated | relid=0 | w=24
  386. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:transthyretin related familial amyloid cardiomyopathy
    n1=en:peutz-jeghers syndrome | n2=en:transthyretin related familial amyloid cardiomyopathy | rel=r_associated | relid=0 | w=24
  387. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:wiskott-aldrich syndrome
    n1=en:peutz-jeghers syndrome | n2=en:wiskott-aldrich syndrome | rel=r_associated | relid=0 | w=24
  388. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:x-linked agammaglobulinemia
    n1=en:peutz-jeghers syndrome | n2=en:x-linked agammaglobulinemia | rel=r_associated | relid=0 | w=24
  389. en:peutz-jeghers syndrome -- r_associated #0: 24 / 0.462 -> en:zimmerman laband syndrome
    n1=en:peutz-jeghers syndrome | n2=en:zimmerman laband syndrome | rel=r_associated | relid=0 | w=24
  390. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> atrophie
    n1=en:peutz-jeghers syndrome | n2=atrophie | rel=r_associated | relid=0 | w=23
  391. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:acrocallosal syndrome
    n1=en:peutz-jeghers syndrome | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=23
  392. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
    n1=en:peutz-jeghers syndrome | n2=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | rel=r_associated | relid=0 | w=23
  393. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:aplasia of lacrimal and salivary glands
    n1=en:peutz-jeghers syndrome | n2=en:aplasia of lacrimal and salivary glands | rel=r_associated | relid=0 | w=23
  394. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:autosomal dominant ichthyosis vulgaris
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant ichthyosis vulgaris | rel=r_associated | relid=0 | w=23
  395. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:autosomal dominant oculocutaneous albinism
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant oculocutaneous albinism | rel=r_associated | relid=0 | w=23
  396. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:bannayan syndrome
    n1=en:peutz-jeghers syndrome | n2=en:bannayan syndrome | rel=r_associated | relid=0 | w=23
  397. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:benign autosomal dominant osteopetrosis
    n1=en:peutz-jeghers syndrome | n2=en:benign autosomal dominant osteopetrosis | rel=r_associated | relid=0 | w=23
  398. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:brown-vialetto-van laere syndrome
    n1=en:peutz-jeghers syndrome | n2=en:brown-vialetto-van laere syndrome | rel=r_associated | relid=0 | w=23
  399. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:charcot-marie-tooth disease type 2d
    n1=en:peutz-jeghers syndrome | n2=en:charcot-marie-tooth disease type 2d | rel=r_associated | relid=0 | w=23
  400. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:charcot-marie-tooth disease, axonal, type 2l (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | rel=r_associated | relid=0 | w=23
  401. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:cherubism
    n1=en:peutz-jeghers syndrome | n2=en:cherubism | rel=r_associated | relid=0 | w=23
  402. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:cochleosaccular degeneration of the inner ear and progressive cataracts
    n1=en:peutz-jeghers syndrome | n2=en:cochleosaccular degeneration of the inner ear and progressive cataracts | rel=r_associated | relid=0 | w=23
  403. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:congenital syphilitic mucous patches
    n1=en:peutz-jeghers syndrome | n2=en:congenital syphilitic mucous patches | rel=r_associated | relid=0 | w=23
  404. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:dyskeratosis congenita, autosomal dominant
    n1=en:peutz-jeghers syndrome | n2=en:dyskeratosis congenita, autosomal dominant | rel=r_associated | relid=0 | w=23
  405. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:dystrophic cardiomyopathy
    n1=en:peutz-jeghers syndrome | n2=en:dystrophic cardiomyopathy | rel=r_associated | relid=0 | w=23
  406. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:ectodermal dysplasia with natal teeth, turnpenny type
    n1=en:peutz-jeghers syndrome | n2=en:ectodermal dysplasia with natal teeth, turnpenny type | rel=r_associated | relid=0 | w=23
  407. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:familial papillary thyroid carcinoma with renal papillary neoplasia syndrome
    n1=en:peutz-jeghers syndrome | n2=en:familial papillary thyroid carcinoma with renal papillary neoplasia syndrome | rel=r_associated | relid=0 | w=23
  408. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:fatty acid hydroxylase-associated neurodegeneration
    n1=en:peutz-jeghers syndrome | n2=en:fatty acid hydroxylase-associated neurodegeneration | rel=r_associated | relid=0 | w=23
  409. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:genital lichen sclerosus
    n1=en:peutz-jeghers syndrome | n2=en:genital lichen sclerosus | rel=r_associated | relid=0 | w=23
  410. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:hereditary nonpolyposis colorectal cancer
    n1=en:peutz-jeghers syndrome | n2=en:hereditary nonpolyposis colorectal cancer | rel=r_associated | relid=0 | w=23
  411. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:heritable pulmonary arterial hypertension due to bmpr2 mutation
    n1=en:peutz-jeghers syndrome | n2=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | rel=r_associated | relid=0 | w=23
  412. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:hyaline dystrophy of bruch's membrane
    n1=en:peutz-jeghers syndrome | n2=en:hyaline dystrophy of bruch's membrane | rel=r_associated | relid=0 | w=23
  413. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:hyperparathyroidism-jaw tumor syndrome
    n1=en:peutz-jeghers syndrome | n2=en:hyperparathyroidism-jaw tumor syndrome | rel=r_associated | relid=0 | w=23
  414. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1
    n1=en:peutz-jeghers syndrome | n2=en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 | rel=r_associated | relid=0 | w=23
  415. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:isaacs syndrome
    n1=en:peutz-jeghers syndrome | n2=en:isaacs syndrome | rel=r_associated | relid=0 | w=23
  416. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:juvenile osteochondrosis of foot, nos
    n1=en:peutz-jeghers syndrome | n2=en:juvenile osteochondrosis of foot, nos | rel=r_associated | relid=0 | w=23
  417. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:kernicterus
    n1=en:peutz-jeghers syndrome | n2=en:kernicterus | rel=r_associated | relid=0 | w=23
  418. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:melanoma astrocytoma syndrome
    n1=en:peutz-jeghers syndrome | n2=en:melanoma astrocytoma syndrome | rel=r_associated | relid=0 | w=23
  419. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:microcephaly, amish type (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:microcephaly, amish type (disorder) | rel=r_associated | relid=0 | w=23
  420. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:neurocutaneous melanosis sequence
    n1=en:peutz-jeghers syndrome | n2=en:neurocutaneous melanosis sequence | rel=r_associated | relid=0 | w=23
  421. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:neurodegeneration with brain iron accumulation 4
    n1=en:peutz-jeghers syndrome | n2=en:neurodegeneration with brain iron accumulation 4 | rel=r_associated | relid=0 | w=23
  422. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:neurofibromatosis type 1
    n1=en:peutz-jeghers syndrome | n2=en:neurofibromatosis type 1 | rel=r_associated | relid=0 | w=23
  423. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:neurofibromatosis, type 1-like syndrome
    n1=en:peutz-jeghers syndrome | n2=en:neurofibromatosis, type 1-like syndrome | rel=r_associated | relid=0 | w=23
  424. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:north american indian childhood cirrhosis
    n1=en:peutz-jeghers syndrome | n2=en:north american indian childhood cirrhosis | rel=r_associated | relid=0 | w=23
  425. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:pancreatic cyst rupture
    n1=en:peutz-jeghers syndrome | n2=en:pancreatic cyst rupture | rel=r_associated | relid=0 | w=23
  426. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:persistent acantholytic dermatosis of fawcett and miller
    n1=en:peutz-jeghers syndrome | n2=en:persistent acantholytic dermatosis of fawcett and miller | rel=r_associated | relid=0 | w=23
  427. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:prickle1-related progressive myoclonus epilepsy with ataxia
    n1=en:peutz-jeghers syndrome | n2=en:prickle1-related progressive myoclonus epilepsy with ataxia | rel=r_associated | relid=0 | w=23
  428. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:reardon hall slaney syndrome
    n1=en:peutz-jeghers syndrome | n2=en:reardon hall slaney syndrome | rel=r_associated | relid=0 | w=23
  429. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:spinocerebellar ataxia 28
    n1=en:peutz-jeghers syndrome | n2=en:spinocerebellar ataxia 28 | rel=r_associated | relid=0 | w=23
  430. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:spinocerebellar ataxia 8
    n1=en:peutz-jeghers syndrome | n2=en:spinocerebellar ataxia 8 | rel=r_associated | relid=0 | w=23
  431. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:spondylocostal dysostosis 4, autosomal dominant
    n1=en:peutz-jeghers syndrome | n2=en:spondylocostal dysostosis 4, autosomal dominant | rel=r_associated | relid=0 | w=23
  432. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:vitiligo iridis
    n1=en:peutz-jeghers syndrome | n2=en:vitiligo iridis | rel=r_associated | relid=0 | w=23
  433. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> en:zosteriform reticulate hyperpigmentation
    n1=en:peutz-jeghers syndrome | n2=en:zosteriform reticulate hyperpigmentation | rel=r_associated | relid=0 | w=23
  434. en:peutz-jeghers syndrome -- r_associated #0: 23 / 0.442 -> maladie de Marfan
    n1=en:peutz-jeghers syndrome | n2=maladie de Marfan | rel=r_associated | relid=0 | w=23
  435. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:autosomal dominant hyperinsulinism due to sur1 deficiency
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant hyperinsulinism due to sur1 deficiency | rel=r_associated | relid=0 | w=22
  436. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:autosomal dominant ichthyosis
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant ichthyosis | rel=r_associated | relid=0 | w=22
  437. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:autosomal dominant mutilating keratoderma
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant mutilating keratoderma | rel=r_associated | relid=0 | w=22
  438. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:behrens baumann dust syndrome
    n1=en:peutz-jeghers syndrome | n2=en:behrens baumann dust syndrome | rel=r_associated | relid=0 | w=22
  439. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:bilateral pheochromocytoma and islet cell adenoma of the pancreas
    n1=en:peutz-jeghers syndrome | n2=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | rel=r_associated | relid=0 | w=22
  440. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:centronuclear myopathy 1
    n1=en:peutz-jeghers syndrome | n2=en:centronuclear myopathy 1 | rel=r_associated | relid=0 | w=22
  441. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:charcot-marie-tooth disease, axonal, type 2b (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | rel=r_associated | relid=0 | w=22
  442. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:charcot-marie-tooth disease, type 2j
    n1=en:peutz-jeghers syndrome | n2=en:charcot-marie-tooth disease, type 2j | rel=r_associated | relid=0 | w=22
  443. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:chromosome 22q11.2 microduplication syndrome
    n1=en:peutz-jeghers syndrome | n2=en:chromosome 22q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=22
  444. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:circumscribed hypermelanosis
    n1=en:peutz-jeghers syndrome | n2=en:circumscribed hypermelanosis | rel=r_associated | relid=0 | w=22
  445. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:cockayne syndrome
    n1=en:peutz-jeghers syndrome | n2=en:cockayne syndrome | rel=r_associated | relid=0 | w=22
  446. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:crisponi syndrome
    n1=en:peutz-jeghers syndrome | n2=en:crisponi syndrome | rel=r_associated | relid=0 | w=22
  447. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:depigmentation
    n1=en:peutz-jeghers syndrome | n2=en:depigmentation | rel=r_associated | relid=0 | w=22
  448. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:dubin-johnson syndrome
    n1=en:peutz-jeghers syndrome | n2=en:dubin-johnson syndrome | rel=r_associated | relid=0 | w=22
  449. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:epidemiologic
    n1=en:peutz-jeghers syndrome | n2=en:epidemiologic | rel=r_associated | relid=0 | w=22
  450. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:epithelial recurrent erosion dystrophy
    n1=en:peutz-jeghers syndrome | n2=en:epithelial recurrent erosion dystrophy | rel=r_associated | relid=0 | w=22
  451. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:ethnologic
    n1=en:peutz-jeghers syndrome | n2=en:ethnologic | rel=r_associated | relid=0 | w=22
  452. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:familial benign neonatal epilepsy
    n1=en:peutz-jeghers syndrome | n2=en:familial benign neonatal epilepsy | rel=r_associated | relid=0 | w=22
  453. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:familial creutzfeldt-jakob
    n1=en:peutz-jeghers syndrome | n2=en:familial creutzfeldt-jakob | rel=r_associated | relid=0 | w=22
  454. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:familial encephalopathy with neuroserpin inclusion bodies
    n1=en:peutz-jeghers syndrome | n2=en:familial encephalopathy with neuroserpin inclusion bodies | rel=r_associated | relid=0 | w=22
  455. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:familial isolated arrhythmogenic right ventricular dysplasia
    n1=en:peutz-jeghers syndrome | n2=en:familial isolated arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=22
  456. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:feingold syndrome
    n1=en:peutz-jeghers syndrome | n2=en:feingold syndrome | rel=r_associated | relid=0 | w=22
  457. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:frontotemporal dementia
    n1=en:peutz-jeghers syndrome | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=22
  458. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:frontotemporal dementia, chromosome 3-linked
    n1=en:peutz-jeghers syndrome | n2=en:frontotemporal dementia, chromosome 3-linked | rel=r_associated | relid=0 | w=22
  459. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related
    n1=en:peutz-jeghers syndrome | n2=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | rel=r_associated | relid=0 | w=22
  460. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:goniodysgenesis-mental retardation-short stature syndrome
    n1=en:peutz-jeghers syndrome | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=22
  461. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:hereditary hemorrhagic telangiectasia
    n1=en:peutz-jeghers syndrome | n2=en:hereditary hemorrhagic telangiectasia | rel=r_associated | relid=0 | w=22
  462. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:hereditary motor and sensory neuropathy type i
    n1=en:peutz-jeghers syndrome | n2=en:hereditary motor and sensory neuropathy type i | rel=r_associated | relid=0 | w=22
  463. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:hereditary stomatocytosis
    n1=en:peutz-jeghers syndrome | n2=en:hereditary stomatocytosis | rel=r_associated | relid=0 | w=22
  464. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:iris coloboma with ptosis, hypertelorism, and mental retardation
    n1=en:peutz-jeghers syndrome | n2=en:iris coloboma with ptosis, hypertelorism, and mental retardation | rel=r_associated | relid=0 | w=22
  465. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:li-fraumeni syndrome
    n1=en:peutz-jeghers syndrome | n2=en:li-fraumeni syndrome | rel=r_associated | relid=0 | w=22
  466. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:linear iga bullous dermatosis
    n1=en:peutz-jeghers syndrome | n2=en:linear iga bullous dermatosis | rel=r_associated | relid=0 | w=22
  467. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:masa syndrome (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:masa syndrome (disorder) | rel=r_associated | relid=0 | w=22
  468. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:melanosis of vulva
    n1=en:peutz-jeghers syndrome | n2=en:melanosis of vulva | rel=r_associated | relid=0 | w=22
  469. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:microcephaly-capillary malformation syndrome
    n1=en:peutz-jeghers syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  470. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:moloney syndrome
    n1=en:peutz-jeghers syndrome | n2=en:moloney syndrome | rel=r_associated | relid=0 | w=22
  471. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:muller-weiss disease
    n1=en:peutz-jeghers syndrome | n2=en:muller-weiss disease | rel=r_associated | relid=0 | w=22
  472. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:myopathy, distal 2
    n1=en:peutz-jeghers syndrome | n2=en:myopathy, distal 2 | rel=r_associated | relid=0 | w=22
  473. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:nail-patella syndrome
    n1=en:peutz-jeghers syndrome | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=22
  474. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:other specified congenital malformations of digestive system
    n1=en:peutz-jeghers syndrome | n2=en:other specified congenital malformations of digestive system | rel=r_associated | relid=0 | w=22
  475. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:other specified congenital malformations of upper alimentary tract
    n1=en:peutz-jeghers syndrome | n2=en:other specified congenital malformations of upper alimentary tract | rel=r_associated | relid=0 | w=22
  476. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:ovarian sex cord-stromal tumor
    n1=en:peutz-jeghers syndrome | n2=en:ovarian sex cord-stromal tumor | rel=r_associated | relid=0 | w=22
  477. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:parietal foramina
    n1=en:peutz-jeghers syndrome | n2=en:parietal foramina | rel=r_associated | relid=0 | w=22
  478. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:peeling skin syndrome, acral type
    n1=en:peutz-jeghers syndrome | n2=en:peeling skin syndrome, acral type | rel=r_associated | relid=0 | w=22
  479. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:peutz-jeghers polyp of the small intestine
    n1=en:peutz-jeghers syndrome | n2=en:peutz-jeghers polyp of the small intestine | rel=r_associated | relid=0 | w=22
  480. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:pitt-hopkins syndrome
    n1=en:peutz-jeghers syndrome | n2=en:pitt-hopkins syndrome | rel=r_associated | relid=0 | w=22
  481. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:reticulate acropigmentation of kitamura
    n1=en:peutz-jeghers syndrome | n2=en:reticulate acropigmentation of kitamura | rel=r_associated | relid=0 | w=22
  482. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:spinocerebellar ataxia 10
    n1=en:peutz-jeghers syndrome | n2=en:spinocerebellar ataxia 10 | rel=r_associated | relid=0 | w=22
  483. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:spondyloperipheral dysplasia short ulna
    n1=en:peutz-jeghers syndrome | n2=en:spondyloperipheral dysplasia short ulna | rel=r_associated | relid=0 | w=22
  484. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:tropical ataxic neuropathy
    n1=en:peutz-jeghers syndrome | n2=en:tropical ataxic neuropathy | rel=r_associated | relid=0 | w=22
  485. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:tylosis
    n1=en:peutz-jeghers syndrome | n2=en:tylosis | rel=r_associated | relid=0 | w=22
  486. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:vestigial gastrointestinal remnant
    n1=en:peutz-jeghers syndrome | n2=en:vestigial gastrointestinal remnant | rel=r_associated | relid=0 | w=22
  487. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:walker-warburg syndrome
    n1=en:peutz-jeghers syndrome | n2=en:walker-warburg syndrome | rel=r_associated | relid=0 | w=22
  488. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:x-linked dystonia parkinsonism
    n1=en:peutz-jeghers syndrome | n2=en:x-linked dystonia parkinsonism | rel=r_associated | relid=0 | w=22
  489. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:xanthoma tendinosum
    n1=en:peutz-jeghers syndrome | n2=en:xanthoma tendinosum | rel=r_associated | relid=0 | w=22
  490. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> en:xeroderma pigmentosum
    n1=en:peutz-jeghers syndrome | n2=en:xeroderma pigmentosum | rel=r_associated | relid=0 | w=22
  491. en:peutz-jeghers syndrome -- r_associated #0: 22 / 0.423 -> syndrome
    n1=en:peutz-jeghers syndrome | n2=syndrome | rel=r_associated | relid=0 | w=22
  492. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:abdominal wall cyst
    n1=en:peutz-jeghers syndrome | n2=en:abdominal wall cyst | rel=r_associated | relid=0 | w=21
  493. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
    n1=en:peutz-jeghers syndrome | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=21
  494. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:autosomal dominant charcot-marie-tooth disease type 2a1
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant charcot-marie-tooth disease type 2a1 | rel=r_associated | relid=0 | w=21
  495. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:autosomal dominant excess of transthyretin
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant excess of transthyretin | rel=r_associated | relid=0 | w=21
  496. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:autosomal dominant pterygium of conjunctiva
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant pterygium of conjunctiva | rel=r_associated | relid=0 | w=21
  497. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:brachydactyly type a6
    n1=en:peutz-jeghers syndrome | n2=en:brachydactyly type a6 | rel=r_associated | relid=0 | w=21
  498. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:cap myopathy
    n1=en:peutz-jeghers syndrome | n2=en:cap myopathy | rel=r_associated | relid=0 | w=21
  499. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:centrofacial lentiginosis syndrome
    n1=en:peutz-jeghers syndrome | n2=en:centrofacial lentiginosis syndrome | rel=r_associated | relid=0 | w=21
  500. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:cerebellar ataxia, cayman type
    n1=en:peutz-jeghers syndrome | n2=en:cerebellar ataxia, cayman type | rel=r_associated | relid=0 | w=21
  501. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:complication aspects
    n1=en:peutz-jeghers syndrome | n2=en:complication aspects | rel=r_associated | relid=0 | w=21
  502. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:congenital reticular ichthyosiform erythroderma
    n1=en:peutz-jeghers syndrome | n2=en:congenital reticular ichthyosiform erythroderma | rel=r_associated | relid=0 | w=21
  503. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:currarino triad
    n1=en:peutz-jeghers syndrome | n2=en:currarino triad | rel=r_associated | relid=0 | w=21
  504. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:fatal familial insomnia
    n1=en:peutz-jeghers syndrome | n2=en:fatal familial insomnia | rel=r_associated | relid=0 | w=21
  505. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:geniospasm 1
    n1=en:peutz-jeghers syndrome | n2=en:geniospasm 1 | rel=r_associated | relid=0 | w=21
  506. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:hawkinsinuria
    n1=en:peutz-jeghers syndrome | n2=en:hawkinsinuria | rel=r_associated | relid=0 | w=21
  507. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:hereditary gastrogenic lactose intolerance
    n1=en:peutz-jeghers syndrome | n2=en:hereditary gastrogenic lactose intolerance | rel=r_associated | relid=0 | w=21
  508. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:hereditary motor neuron disease
    n1=en:peutz-jeghers syndrome | n2=en:hereditary motor neuron disease | rel=r_associated | relid=0 | w=21
  509. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:hereditary palmoplantar keratoderma gamborg nielsen type
    n1=en:peutz-jeghers syndrome | n2=en:hereditary palmoplantar keratoderma gamborg nielsen type | rel=r_associated | relid=0 | w=21
  510. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:hereditary sensory autonomic neuropathy, type 1
    n1=en:peutz-jeghers syndrome | n2=en:hereditary sensory autonomic neuropathy, type 1 | rel=r_associated | relid=0 | w=21
  511. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:hyperinsulinemic hypoglycemia, familial, 6
    n1=en:peutz-jeghers syndrome | n2=en:hyperinsulinemic hypoglycemia, familial, 6 | rel=r_associated | relid=0 | w=21
  512. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:hyperinsulinemic hypoglycemia, familial, 7
    n1=en:peutz-jeghers syndrome | n2=en:hyperinsulinemic hypoglycemia, familial, 7 | rel=r_associated | relid=0 | w=21
  513. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
    n1=en:peutz-jeghers syndrome | n2=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | rel=r_associated | relid=0 | w=21
  514. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:leukotriene c4 synthase deficiency
    n1=en:peutz-jeghers syndrome | n2=en:leukotriene c4 synthase deficiency | rel=r_associated | relid=0 | w=21
  515. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:may-hegglin anomaly
    n1=en:peutz-jeghers syndrome | n2=en:may-hegglin anomaly | rel=r_associated | relid=0 | w=21
  516. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:metaphyseal dysplasia, braun-tinschert type
    n1=en:peutz-jeghers syndrome | n2=en:metaphyseal dysplasia, braun-tinschert type | rel=r_associated | relid=0 | w=21
  517. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:microcephaly deafness syndrome
    n1=en:peutz-jeghers syndrome | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=21
  518. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:microcephaly microcornea syndrome seemanova type
    n1=en:peutz-jeghers syndrome | n2=en:microcephaly microcornea syndrome seemanova type | rel=r_associated | relid=0 | w=21
  519. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:microvillus inclusion disease
    n1=en:peutz-jeghers syndrome | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=21
  520. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:multiple epiphyseal dysplasia type 5
    n1=en:peutz-jeghers syndrome | n2=en:multiple epiphyseal dysplasia type 5 | rel=r_associated | relid=0 | w=21
  521. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:ohdo syndrome, maat-kievit-brunner type
    n1=en:peutz-jeghers syndrome | n2=en:ohdo syndrome, maat-kievit-brunner type | rel=r_associated | relid=0 | w=21
  522. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:osteogenesis imperfecta, levin type
    n1=en:peutz-jeghers syndrome | n2=en:osteogenesis imperfecta, levin type | rel=r_associated | relid=0 | w=21
  523. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:osteomalacia
    n1=en:peutz-jeghers syndrome | n2=en:osteomalacia | rel=r_associated | relid=0 | w=21
  524. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:post-inflammatory hyperpigmentation in lichen planus
    n1=en:peutz-jeghers syndrome | n2=en:post-inflammatory hyperpigmentation in lichen planus | rel=r_associated | relid=0 | w=21
  525. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:pulmonary alveolar proteinosis, acquired
    n1=en:peutz-jeghers syndrome | n2=en:pulmonary alveolar proteinosis, acquired | rel=r_associated | relid=0 | w=21
  526. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:spinocerebellar ataxia type 7
    n1=en:peutz-jeghers syndrome | n2=en:spinocerebellar ataxia type 7 | rel=r_associated | relid=0 | w=21
  527. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:tarsal-carpal coalition syndrome
    n1=en:peutz-jeghers syndrome | n2=en:tarsal-carpal coalition syndrome | rel=r_associated | relid=0 | w=21
  528. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:tungland bellman syndrome
    n1=en:peutz-jeghers syndrome | n2=en:tungland bellman syndrome | rel=r_associated | relid=0 | w=21
  529. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:type i acrocephalosyndactyly
    n1=en:peutz-jeghers syndrome | n2=en:type i acrocephalosyndactyly | rel=r_associated | relid=0 | w=21
  530. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:type v acrocephalosyndactyly
    n1=en:peutz-jeghers syndrome | n2=en:type v acrocephalosyndactyly | rel=r_associated | relid=0 | w=21
  531. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:vascular neurocutaneous syndrome
    n1=en:peutz-jeghers syndrome | n2=en:vascular neurocutaneous syndrome | rel=r_associated | relid=0 | w=21
  532. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:verruciform xanthoma of oral mucous membrane
    n1=en:peutz-jeghers syndrome | n2=en:verruciform xanthoma of oral mucous membrane | rel=r_associated | relid=0 | w=21
  533. en:peutz-jeghers syndrome -- r_associated #0: 21 / 0.404 -> en:waardenburg syndrome type 4
    n1=en:peutz-jeghers syndrome | n2=en:waardenburg syndrome type 4 | rel=r_associated | relid=0 | w=21
  534. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> aclasie diaphysaire
    n1=en:peutz-jeghers syndrome | n2=aclasie diaphysaire | rel=r_associated | relid=0 | w=20
  535. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> acrodermatite entéropathique
    n1=en:peutz-jeghers syndrome | n2=acrodermatite entéropathique | rel=r_associated | relid=0 | w=20
  536. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> acrodermatitis enteropathica
    n1=en:peutz-jeghers syndrome | n2=acrodermatitis enteropathica | rel=r_associated | relid=0 | w=20
  537. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> adénomatose rectocolique familiale
    n1=en:peutz-jeghers syndrome | n2=adénomatose rectocolique familiale | rel=r_associated | relid=0 | w=20
  538. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> affections atrophiques de la peau
    n1=en:peutz-jeghers syndrome | n2=affections atrophiques de la peau | rel=r_associated | relid=0 | w=20
  539. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> agranulocytose constitutionnelle
    n1=en:peutz-jeghers syndrome | n2=agranulocytose constitutionnelle | rel=r_associated | relid=0 | w=20
  540. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> albinisme
    n1=en:peutz-jeghers syndrome | n2=albinisme | rel=r_associated | relid=0 | w=20
  541. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> albinisme oculocutané de type mutant jaune
    n1=en:peutz-jeghers syndrome | n2=albinisme oculocutané de type mutant jaune | rel=r_associated | relid=0 | w=20
  542. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> albinoïdisme
    n1=en:peutz-jeghers syndrome | n2=albinoïdisme | rel=r_associated | relid=0 | w=20
  543. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> anémie ferriprive
    n1=en:peutz-jeghers syndrome | n2=anémie ferriprive | rel=r_associated | relid=0 | w=20
  544. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> anomalie du développement
    n1=en:peutz-jeghers syndrome | n2=anomalie du développement | rel=r_associated | relid=0 | w=20
  545. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> anomalies buccales
    n1=en:peutz-jeghers syndrome | n2=anomalies buccales | rel=r_associated | relid=0 | w=20
  546. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> anomalies de la bouche
    n1=en:peutz-jeghers syndrome | n2=anomalies de la bouche | rel=r_associated | relid=0 | w=20
  547. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> anus contre nature
    n1=en:peutz-jeghers syndrome | n2=anus contre nature | rel=r_associated | relid=0 | w=20
  548. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> anus praeter
    n1=en:peutz-jeghers syndrome | n2=anus praeter | rel=r_associated | relid=0 | w=20
  549. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> arachnodactylie
    n1=en:peutz-jeghers syndrome | n2=arachnodactylie | rel=r_associated | relid=0 | w=20
  550. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> artério-sclérose
    n1=en:peutz-jeghers syndrome | n2=artério-sclérose | rel=r_associated | relid=0 | w=20
  551. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> artériosclérose
    n1=en:peutz-jeghers syndrome | n2=artériosclérose | rel=r_associated | relid=0 | w=20
  552. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> atrophie cutanée
    n1=en:peutz-jeghers syndrome | n2=atrophie cutanée | rel=r_associated | relid=0 | w=20
  553. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> atrophie de la peau
    n1=en:peutz-jeghers syndrome | n2=atrophie de la peau | rel=r_associated | relid=0 | w=20
  554. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> atrophie optique
    n1=en:peutz-jeghers syndrome | n2=atrophie optique | rel=r_associated | relid=0 | w=20
  555. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> atrophie optique autosomique dominante
    n1=en:peutz-jeghers syndrome | n2=atrophie optique autosomique dominante | rel=r_associated | relid=0 | w=20
  556. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> atrophie optique congénitale ou infantile précoce
    n1=en:peutz-jeghers syndrome | n2=atrophie optique congénitale ou infantile précoce | rel=r_associated | relid=0 | w=20
  557. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> atrophie optique liée au sexe
    n1=en:peutz-jeghers syndrome | n2=atrophie optique liée au sexe | rel=r_associated | relid=0 | w=20
  558. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> atrophie optique liée au sexe de Völker-Dieben
    n1=en:peutz-jeghers syndrome | n2=atrophie optique liée au sexe de Völker-Dieben | rel=r_associated | relid=0 | w=20
  559. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> atrophie optique polyneuropathie et surdité
    n1=en:peutz-jeghers syndrome | n2=atrophie optique polyneuropathie et surdité | rel=r_associated | relid=0 | w=20
  560. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> atrophie optique tardive liée au sexe
    n1=en:peutz-jeghers syndrome | n2=atrophie optique tardive liée au sexe | rel=r_associated | relid=0 | w=20
  561. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> atrophie optique-paraplégie spastique
    n1=en:peutz-jeghers syndrome | n2=atrophie optique-paraplégie spastique | rel=r_associated | relid=0 | w=20
  562. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> atrophie optique, cataracte, et troubles neurologiques
    n1=en:peutz-jeghers syndrome | n2=atrophie optique, cataracte, et troubles neurologiques | rel=r_associated | relid=0 | w=20
  563. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> atrophie optique, surdité, épilepsie, spasticité et décès précoce
    n1=en:peutz-jeghers syndrome | n2=atrophie optique, surdité, épilepsie, spasticité et décès précoce | rel=r_associated | relid=0 | w=20
  564. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> atrophodermie
    n1=en:peutz-jeghers syndrome | n2=atrophodermie | rel=r_associated | relid=0 | w=20
  565. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> autres anomalies de la pigmentation
    n1=en:peutz-jeghers syndrome | n2=autres anomalies de la pigmentation | rel=r_associated | relid=0 | w=20
  566. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> bilirubinémie
    n1=en:peutz-jeghers syndrome | n2=bilirubinémie | rel=r_associated | relid=0 | w=20
  567. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> bouche
    n1=en:peutz-jeghers syndrome | n2=bouche | rel=r_associated | relid=0 | w=20
  568. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> bran de Judas
    n1=en:peutz-jeghers syndrome | n2=bran de Judas | rel=r_associated | relid=0 | w=20
  569. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> byssinosis
    n1=en:peutz-jeghers syndrome | n2=byssinosis | rel=r_associated | relid=0 | w=20
  570. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> cancer
    n1=en:peutz-jeghers syndrome | n2=cancer | rel=r_associated | relid=0 | w=20
  571. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> cancer colo-rectal héréditaire sans polypose
    n1=en:peutz-jeghers syndrome | n2=cancer colo-rectal héréditaire sans polypose | rel=r_associated | relid=0 | w=20
  572. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Cancer colorectal héréditaire sans polypose
    n1=en:peutz-jeghers syndrome | n2=Cancer colorectal héréditaire sans polypose | rel=r_associated | relid=0 | w=20
  573. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> cancer colorectal héréditaire sans polypose
    n1=en:peutz-jeghers syndrome | n2=cancer colorectal héréditaire sans polypose | rel=r_associated | relid=0 | w=20
  574. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Cancer du pancréas
    n1=en:peutz-jeghers syndrome | n2=Cancer du pancréas | rel=r_associated | relid=0 | w=20
  575. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> cancer du pancréas
    n1=en:peutz-jeghers syndrome | n2=cancer du pancréas | rel=r_associated | relid=0 | w=20
  576. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> cancer pancréatique
    n1=en:peutz-jeghers syndrome | n2=cancer pancréatique | rel=r_associated | relid=0 | w=20
  577. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> cancérologie
    n1=en:peutz-jeghers syndrome | n2=cancérologie | rel=r_associated | relid=0 | w=20
  578. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> carcinologie
    n1=en:peutz-jeghers syndrome | n2=carcinologie | rel=r_associated | relid=0 | w=20
  579. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> carcinome du pancréas
    n1=en:peutz-jeghers syndrome | n2=carcinome du pancréas | rel=r_associated | relid=0 | w=20
  580. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> carcinome du pancreas
    n1=en:peutz-jeghers syndrome | n2=carcinome du pancreas | rel=r_associated | relid=0 | w=20
  581. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> carcinome pancréatique
    n1=en:peutz-jeghers syndrome | n2=carcinome pancréatique | rel=r_associated | relid=0 | w=20
  582. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> cellule de Sertoli
    n1=en:peutz-jeghers syndrome | n2=cellule de Sertoli | rel=r_associated | relid=0 | w=20
  583. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> chérubisme
    n1=en:peutz-jeghers syndrome | n2=chérubisme | rel=r_associated | relid=0 | w=20
  584. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> chondrodysplasie déformante héréditaire
    n1=en:peutz-jeghers syndrome | n2=chondrodysplasie déformante héréditaire | rel=r_associated | relid=0 | w=20
  585. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> chondrodysplasie héréditaire déformante
    n1=en:peutz-jeghers syndrome | n2=chondrodysplasie héréditaire déformante | rel=r_associated | relid=0 | w=20
  586. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> congénital
    n1=en:peutz-jeghers syndrome | n2=congénital | rel=r_associated | relid=0 | w=20
  587. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> congenital
    n1=en:peutz-jeghers syndrome | n2=congenital | rel=r_associated | relid=0 | w=20
  588. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> congénitale
    n1=en:peutz-jeghers syndrome | n2=congénitale | rel=r_associated | relid=0 | w=20
  589. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> contractures congénitales et arachnodactylie
    n1=en:peutz-jeghers syndrome | n2=contractures congénitales et arachnodactylie | rel=r_associated | relid=0 | w=20
  590. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> déficience congénitale
    n1=en:peutz-jeghers syndrome | n2=déficience congénitale | rel=r_associated | relid=0 | w=20
  591. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> déformation congénitale
    n1=en:peutz-jeghers syndrome | n2=déformation congénitale | rel=r_associated | relid=0 | w=20
  592. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> dégénérescence d'un polype sinusien
    n1=en:peutz-jeghers syndrome | n2=dégénérescence d'un polype sinusien | rel=r_associated | relid=0 | w=20
  593. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> dégénérescence polypoïde du sinus
    n1=en:peutz-jeghers syndrome | n2=dégénérescence polypoïde du sinus | rel=r_associated | relid=0 | w=20
  594. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> démence fronto-temporale
    n1=en:peutz-jeghers syndrome | n2=démence fronto-temporale | rel=r_associated | relid=0 | w=20
  595. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> démence frontotemporale
    n1=en:peutz-jeghers syndrome | n2=démence frontotemporale | rel=r_associated | relid=0 | w=20
  596. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> déminéralisation osseuse
    n1=en:peutz-jeghers syndrome | n2=déminéralisation osseuse | rel=r_associated | relid=0 | w=20
  597. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> démyélinisation
    n1=en:peutz-jeghers syndrome | n2=démyélinisation | rel=r_associated | relid=0 | w=20
  598. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> dépigmentation
    n1=en:peutz-jeghers syndrome | n2=dépigmentation | rel=r_associated | relid=0 | w=20
  599. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> dermatologie
    n1=en:peutz-jeghers syndrome | n2=dermatologie | rel=r_associated | relid=0 | w=20
  600. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> difformité congénitale
    n1=en:peutz-jeghers syndrome | n2=difformité congénitale | rel=r_associated | relid=0 | w=20
  601. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> distrophie
    n1=en:peutz-jeghers syndrome | n2=distrophie | rel=r_associated | relid=0 | w=20
  602. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> diverticule de Meckel
    n1=en:peutz-jeghers syndrome | n2=diverticule de Meckel | rel=r_associated | relid=0 | w=20
  603. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Diverticule de Meckel
    n1=en:peutz-jeghers syndrome | n2=Diverticule de Meckel | rel=r_associated | relid=0 | w=20
  604. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> dysplasie acromicrique
    n1=en:peutz-jeghers syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
  605. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> dysplasie cléido-crânienne
    n1=en:peutz-jeghers syndrome | n2=dysplasie cléido-crânienne | rel=r_associated | relid=0 | w=20
  606. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> dysplasie cléidocrânienne
    n1=en:peutz-jeghers syndrome | n2=dysplasie cléidocrânienne | rel=r_associated | relid=0 | w=20
  607. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> dystonie dopasensible
    n1=en:peutz-jeghers syndrome | n2=dystonie dopasensible | rel=r_associated | relid=0 | w=20
  608. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> dystrophie
    n1=en:peutz-jeghers syndrome | n2=dystrophie | rel=r_associated | relid=0 | w=20
  609. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> dystrophie des cônes liée au sexe
    n1=en:peutz-jeghers syndrome | n2=dystrophie des cônes liée au sexe | rel=r_associated | relid=0 | w=20
  610. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> dystrophie des cônes liée au sexe avec reflet rétinien jaune-vert
    n1=en:peutz-jeghers syndrome | n2=dystrophie des cônes liée au sexe avec reflet rétinien jaune-vert | rel=r_associated | relid=0 | w=20
  611. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> dystrophie vulvaire
    n1=en:peutz-jeghers syndrome | n2=dystrophie vulvaire | rel=r_associated | relid=0 | w=20
  612. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> dystrophy
    n1=en:peutz-jeghers syndrome | n2=dystrophy | rel=r_associated | relid=0 | w=20
  613. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:17q11.2 microduplication syndrome
    n1=en:peutz-jeghers syndrome | n2=en:17q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=20
  614. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:absence of fingerprints with congenital milia syndrome
    n1=en:peutz-jeghers syndrome | n2=en:absence of fingerprints with congenital milia syndrome | rel=r_associated | relid=0 | w=20
  615. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:acquired epidermolysis bullosa
    n1=en:peutz-jeghers syndrome | n2=en:acquired epidermolysis bullosa | rel=r_associated | relid=0 | w=20
  616. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:acquired hypopigmentation of choroid
    n1=en:peutz-jeghers syndrome | n2=en:acquired hypopigmentation of choroid | rel=r_associated | relid=0 | w=20
  617. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:acro-dermato-ungual-lacrimal-tooth syndrome
    n1=en:peutz-jeghers syndrome | n2=en:acro-dermato-ungual-lacrimal-tooth syndrome | rel=r_associated | relid=0 | w=20
  618. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein
    n1=en:peutz-jeghers syndrome | n2=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | rel=r_associated | relid=0 | w=20
  619. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:albinism
    n1=en:peutz-jeghers syndrome | n2=en:albinism | rel=r_associated | relid=0 | w=20
  620. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:albinoidism
    n1=en:peutz-jeghers syndrome | n2=en:albinoidism | rel=r_associated | relid=0 | w=20
  621. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:alveolar proteinosis
    n1=en:peutz-jeghers syndrome | n2=en:alveolar proteinosis | rel=r_associated | relid=0 | w=20
  622. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:angina co-occurrent and due to arteriosclerosis of coronary artery bypass graft
    n1=en:peutz-jeghers syndrome | n2=en:angina co-occurrent and due to arteriosclerosis of coronary artery bypass graft | rel=r_associated | relid=0 | w=20
  623. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:aniridia and intellectual disability syndrome
    n1=en:peutz-jeghers syndrome | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=20
  624. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:aniridia, ptosis, intellectual disability, familial obesity syndrome
    n1=en:peutz-jeghers syndrome | n2=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | rel=r_associated | relid=0 | w=20
  625. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges
    n1=en:peutz-jeghers syndrome | n2=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | rel=r_associated | relid=0 | w=20
  626. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:aphalangy and syndactyly with microcephaly syndrome
    n1=en:peutz-jeghers syndrome | n2=en:aphalangy and syndactyly with microcephaly syndrome | rel=r_associated | relid=0 | w=20
  627. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:application site pigmentation changes
    n1=en:peutz-jeghers syndrome | n2=en:application site pigmentation changes | rel=r_associated | relid=0 | w=20
  628. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:arachnodactily
    n1=en:peutz-jeghers syndrome | n2=en:arachnodactily | rel=r_associated | relid=0 | w=20
  629. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:arachnodactyly
    n1=en:peutz-jeghers syndrome | n2=en:arachnodactyly | rel=r_associated | relid=0 | w=20
  630. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:argyria
    n1=en:peutz-jeghers syndrome | n2=en:argyria | rel=r_associated | relid=0 | w=20
  631. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:arterial dissection and lentiginosis syndrome
    n1=en:peutz-jeghers syndrome | n2=en:arterial dissection and lentiginosis syndrome | rel=r_associated | relid=0 | w=20
  632. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:arteriosclerosis
    n1=en:peutz-jeghers syndrome | n2=en:arteriosclerosis | rel=r_associated | relid=0 | w=20
  633. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:atrophia
    n1=en:peutz-jeghers syndrome | n2=en:atrophia | rel=r_associated | relid=0 | w=20
  634. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:atrophic fibrosis of lung
    n1=en:peutz-jeghers syndrome | n2=en:atrophic fibrosis of lung | rel=r_associated | relid=0 | w=20
  635. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:atrophic thrush
    n1=en:peutz-jeghers syndrome | n2=en:atrophic thrush | rel=r_associated | relid=0 | w=20
  636. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:atrophoderma
    n1=en:peutz-jeghers syndrome | n2=en:atrophoderma | rel=r_associated | relid=0 | w=20
  637. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:atrophy of salivary gland
    n1=en:peutz-jeghers syndrome | n2=en:atrophy of salivary gland | rel=r_associated | relid=0 | w=20
  638. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:atrophy of soft tissue of orbit
    n1=en:peutz-jeghers syndrome | n2=en:atrophy of soft tissue of orbit | rel=r_associated | relid=0 | w=20
  639. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:atrophy of vulva
    n1=en:peutz-jeghers syndrome | n2=en:atrophy of vulva | rel=r_associated | relid=0 | w=20
  640. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:attenuated familial adenomatous polyposis
    n1=en:peutz-jeghers syndrome | n2=en:attenuated familial adenomatous polyposis | rel=r_associated | relid=0 | w=20
  641. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:autosomal dominant beta2-microglobulinic amyloidosis
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant beta2-microglobulinic amyloidosis | rel=r_associated | relid=0 | w=20
  642. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20
  643. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:autosomal dominant charcot-marie-tooth disease type 2m
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant charcot-marie-tooth disease type 2m | rel=r_associated | relid=0 | w=20
  644. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:autosomal dominant focal dystonia dyt25 type
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant focal dystonia dyt25 type | rel=r_associated | relid=0 | w=20
  645. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:autosomal dominant inheritance
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant inheritance | rel=r_associated | relid=0 | w=20
  646. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:autosomal dominant palmoplantar keratoderma and congenital alopecia
    n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | rel=r_associated | relid=0 | w=20
  647. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:bamforth syndrome
    n1=en:peutz-jeghers syndrome | n2=en:bamforth syndrome | rel=r_associated | relid=0 | w=20
  648. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:basal cell nevus syndrome
    n1=en:peutz-jeghers syndrome | n2=en:basal cell nevus syndrome | rel=r_associated | relid=0 | w=20
  649. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:basal epidermolysis bullosa simplex
    n1=en:peutz-jeghers syndrome | n2=en:basal epidermolysis bullosa simplex | rel=r_associated | relid=0 | w=20
  650. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:benign tumor of pancreas
    n1=en:peutz-jeghers syndrome | n2=en:benign tumor of pancreas | rel=r_associated | relid=0 | w=20
  651. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:bethlem myopathy 1
    n1=en:peutz-jeghers syndrome | n2=en:bethlem myopathy 1 | rel=r_associated | relid=0 | w=20
  652. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:birnbaum's syndrome
    n1=en:peutz-jeghers syndrome | n2=en:birnbaum's syndrome | rel=r_associated | relid=0 | w=20
  653. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:birt-hogg-dube syndrome
    n1=en:peutz-jeghers syndrome | n2=en:birt-hogg-dube syndrome | rel=r_associated | relid=0 | w=20
  654. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:birth defect
    n1=en:peutz-jeghers syndrome | n2=en:birth defect | rel=r_associated | relid=0 | w=20
  655. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:birth mark
    n1=en:peutz-jeghers syndrome | n2=en:birth mark | rel=r_associated | relid=0 | w=20
  656. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:brachytelephalangy, facial dysmorphism, kallmann syndrome
    n1=en:peutz-jeghers syndrome | n2=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | rel=r_associated | relid=0 | w=20
  657. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:brain calcification rajab type
    n1=en:peutz-jeghers syndrome | n2=en:brain calcification rajab type | rel=r_associated | relid=0 | w=20
  658. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:breast atrophy
    n1=en:peutz-jeghers syndrome | n2=en:breast atrophy | rel=r_associated | relid=0 | w=20
  659. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:breast carcinoma
    n1=en:peutz-jeghers syndrome | n2=en:breast carcinoma | rel=r_associated | relid=0 | w=20
  660. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:byssinosis
    n1=en:peutz-jeghers syndrome | n2=en:byssinosis | rel=r_associated | relid=0 | w=20
  661. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:cardiac anomaly and heterotaxy syndrome
    n1=en:peutz-jeghers syndrome | n2=en:cardiac anomaly and heterotaxy syndrome | rel=r_associated | relid=0 | w=20
  662. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:carney-stratakis syndrome
    n1=en:peutz-jeghers syndrome | n2=en:carney-stratakis syndrome | rel=r_associated | relid=0 | w=20
  663. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:cataract glaucoma syndrome
    n1=en:peutz-jeghers syndrome | n2=en:cataract glaucoma syndrome | rel=r_associated | relid=0 | w=20
  664. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:central nervous system degenerative disorder
    n1=en:peutz-jeghers syndrome | n2=en:central nervous system degenerative disorder | rel=r_associated | relid=0 | w=20
  665. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:cerebral gigantism
    n1=en:peutz-jeghers syndrome | n2=en:cerebral gigantism | rel=r_associated | relid=0 | w=20
  666. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:cervical carcinoma
    n1=en:peutz-jeghers syndrome | n2=en:cervical carcinoma | rel=r_associated | relid=0 | w=20
  667. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:cervical hypertrichosis and peripheral neuropathy syndrome
    n1=en:peutz-jeghers syndrome | n2=en:cervical hypertrichosis and peripheral neuropathy syndrome | rel=r_associated | relid=0 | w=20
  668. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:choledochal cyst
    n1=en:peutz-jeghers syndrome | n2=en:choledochal cyst | rel=r_associated | relid=0 | w=20
  669. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:chronic berylliosis
    n1=en:peutz-jeghers syndrome | n2=en:chronic berylliosis | rel=r_associated | relid=0 | w=20
  670. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:chronic diarrhea with villous atrophy syndrome
    n1=en:peutz-jeghers syndrome | n2=en:chronic diarrhea with villous atrophy syndrome | rel=r_associated | relid=0 | w=20
  671. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:cleidorhizomelic syndrome
    n1=en:peutz-jeghers syndrome | n2=en:cleidorhizomelic syndrome | rel=r_associated | relid=0 | w=20
  672. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:complex regional pain syndrome i
    n1=en:peutz-jeghers syndrome | n2=en:complex regional pain syndrome i | rel=r_associated | relid=0 | w=20
  673. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:cone-dystrophy
    n1=en:peutz-jeghers syndrome | n2=en:cone-dystrophy | rel=r_associated | relid=0 | w=20
  674. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:congenital anomaly
    n1=en:peutz-jeghers syndrome | n2=en:congenital anomaly | rel=r_associated | relid=0 | w=20
  675. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:congenital defect
    n1=en:peutz-jeghers syndrome | n2=en:congenital defect | rel=r_associated | relid=0 | w=20
  676. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:congenital enterocyte heparan sulfate deficiency
    n1=en:peutz-jeghers syndrome | n2=en:congenital enterocyte heparan sulfate deficiency | rel=r_associated | relid=0 | w=20
  677. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:congenital ichthyosis
    n1=en:peutz-jeghers syndrome | n2=en:congenital ichthyosis | rel=r_associated | relid=0 | w=20
  678. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:congenital malformation
    n1=en:peutz-jeghers syndrome | n2=en:congenital malformation | rel=r_associated | relid=0 | w=20
  679. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:congenital neutropenia
    n1=en:peutz-jeghers syndrome | n2=en:congenital neutropenia | rel=r_associated | relid=0 | w=20
  680. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:congenital osteodystrophy
    n1=en:peutz-jeghers syndrome | n2=en:congenital osteodystrophy | rel=r_associated | relid=0 | w=20
  681. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:congenital pigmentary skin anomalies
    n1=en:peutz-jeghers syndrome | n2=en:congenital pigmentary skin anomalies | rel=r_associated | relid=0 | w=20
  682. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:conjunctival pigmentation
    n1=en:peutz-jeghers syndrome | n2=en:conjunctival pigmentation | rel=r_associated | relid=0 | w=20
  683. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:constitutional mismatch repair deficiency syndrome
    n1=en:peutz-jeghers syndrome | n2=en:constitutional mismatch repair deficiency syndrome | rel=r_associated | relid=0 | w=20
  684. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:corneal dystrophy, subepithelial mucinous
    n1=en:peutz-jeghers syndrome | n2=en:corneal dystrophy, subepithelial mucinous | rel=r_associated | relid=0 | w=20
  685. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:costello syndrome
    n1=en:peutz-jeghers syndrome | n2=en:costello syndrome | rel=r_associated | relid=0 | w=20
  686. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:cowden syndrome
    n1=en:peutz-jeghers syndrome | n2=en:cowden syndrome | rel=r_associated | relid=0 | w=20
  687. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:craniosynostosis with facial dysmorphism and brachydactyly syndrome
    n1=en:peutz-jeghers syndrome | n2=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | rel=r_associated | relid=0 | w=20
  688. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:crystal arthropathy
    n1=en:peutz-jeghers syndrome | n2=en:crystal arthropathy | rel=r_associated | relid=0 | w=20
  689. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:cutaneous photosensitivity and lethal colitis syndrome
    n1=en:peutz-jeghers syndrome | n2=en:cutaneous photosensitivity and lethal colitis syndrome | rel=r_associated | relid=0 | w=20
  690. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:czech dysplasia, metatarsal type
    n1=en:peutz-jeghers syndrome | n2=en:czech dysplasia, metatarsal type | rel=r_associated | relid=0 | w=20
  691. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:de toni-debre-fanconi syndrome
    n1=en:peutz-jeghers syndrome | n2=en:de toni-debre-fanconi syndrome | rel=r_associated | relid=0 | w=20
  692. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:deafness
    n1=en:peutz-jeghers syndrome | n2=en:deafness | rel=r_associated | relid=0 | w=20
  693. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:degenerative and/or vascular disorder of ear
    n1=en:peutz-jeghers syndrome | n2=en:degenerative and/or vascular disorder of ear | rel=r_associated | relid=0 | w=20
  694. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:degenerative disorder of eye
    n1=en:peutz-jeghers syndrome | n2=en:degenerative disorder of eye | rel=r_associated | relid=0 | w=20
  695. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:demyelinating disorder of central nervous system
    n1=en:peutz-jeghers syndrome | n2=en:demyelinating disorder of central nervous system | rel=r_associated | relid=0 | w=20
  696. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:demyelinating polyneuropathy
    n1=en:peutz-jeghers syndrome | n2=en:demyelinating polyneuropathy | rel=r_associated | relid=0 | w=20
  697. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:demyelination
    n1=en:peutz-jeghers syndrome | n2=en:demyelination | rel=r_associated | relid=0 | w=20
  698. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
    n1=en:peutz-jeghers syndrome | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=20
  699. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:denys-drash syndrome
    n1=en:peutz-jeghers syndrome | n2=en:denys-drash syndrome | rel=r_associated | relid=0 | w=20
  700. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:developmental absence of tooth
    n1=en:peutz-jeghers syndrome | n2=en:developmental absence of tooth | rel=r_associated | relid=0 | w=20
  701. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:developmental anomaly
    n1=en:peutz-jeghers syndrome | n2=en:developmental anomaly | rel=r_associated | relid=0 | w=20
  702. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:developmental fault
    n1=en:peutz-jeghers syndrome | n2=en:developmental fault | rel=r_associated | relid=0 | w=20
  703. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:diffuse palmoplantar keratoderma and acrocyanosis syndrome
    n1=en:peutz-jeghers syndrome | n2=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | rel=r_associated | relid=0 | w=20
  704. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:digestive system neoplasm
    n1=en:peutz-jeghers syndrome | n2=en:digestive system neoplasm | rel=r_associated | relid=0 | w=20
  705. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:discrete intestinal polyps
    n1=en:peutz-jeghers syndrome | n2=en:discrete intestinal polyps | rel=r_associated | relid=0 | w=20
  706. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Dubin-Johnson's syndrome
    n1=en:peutz-jeghers syndrome | n2=en:Dubin-Johnson's syndrome | rel=r_associated | relid=0 | w=20
  707. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Dubin-Sprinz disease
    n1=en:peutz-jeghers syndrome | n2=en:Dubin-Sprinz disease | rel=r_associated | relid=0 | w=20
  708. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:dyschondrosteosis and nephritis syndrome
    n1=en:peutz-jeghers syndrome | n2=en:dyschondrosteosis and nephritis syndrome | rel=r_associated | relid=0 | w=20
  709. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:dysplastic nevus syndrome
    n1=en:peutz-jeghers syndrome | n2=en:dysplastic nevus syndrome | rel=r_associated | relid=0 | w=20
  710. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:dystrophy
    n1=en:peutz-jeghers syndrome | n2=en:dystrophy | rel=r_associated | relid=0 | w=20
  711. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:ectodermal dysplasia with blindness syndrome
    n1=en:peutz-jeghers syndrome | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20
  712. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:ehlers-danlos syndrome vascular-like type
    n1=en:peutz-jeghers syndrome | n2=en:ehlers-danlos syndrome vascular-like type | rel=r_associated | relid=0 | w=20
  713. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:emberger syndrome
    n1=en:peutz-jeghers syndrome | n2=en:emberger syndrome | rel=r_associated | relid=0 | w=20
  714. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:epidemiological
    n1=en:peutz-jeghers syndrome | n2=en:epidemiological | rel=r_associated | relid=0 | w=20
  715. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:epidermolysis bullosa acquisita
    n1=en:peutz-jeghers syndrome | n2=en:epidermolysis bullosa acquisita | rel=r_associated | relid=0 | w=20
  716. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:epiphyseal dysplasia, multiple, 2
    n1=en:peutz-jeghers syndrome | n2=en:epiphyseal dysplasia, multiple, 2 | rel=r_associated | relid=0 | w=20
  717. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:etat criblé
    n1=en:peutz-jeghers syndrome | n2=en:etat criblé | rel=r_associated | relid=0 | w=20
  718. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:exania
    n1=en:peutz-jeghers syndrome | n2=en:exania | rel=r_associated | relid=0 | w=20
  719. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:extraosseous calcification
    n1=en:peutz-jeghers syndrome | n2=en:extraosseous calcification | rel=r_associated | relid=0 | w=20
  720. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:eyelid xanthoma
    n1=en:peutz-jeghers syndrome | n2=en:eyelid xanthoma | rel=r_associated | relid=0 | w=20
  721. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:familial acute myeloid leukemia
    n1=en:peutz-jeghers syndrome | n2=en:familial acute myeloid leukemia | rel=r_associated | relid=0 | w=20
  722. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:familial adenomatous polyposis
    n1=en:peutz-jeghers syndrome | n2=en:familial adenomatous polyposis | rel=r_associated | relid=0 | w=20
  723. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:familial arthrogryposis-cholestatic hepatorenal syndrome
    n1=en:peutz-jeghers syndrome | n2=en:familial arthrogryposis-cholestatic hepatorenal syndrome | rel=r_associated | relid=0 | w=20
  724. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:familial chronic lymphocytic leukemia
    n1=en:peutz-jeghers syndrome | n2=en:familial chronic lymphocytic leukemia | rel=r_associated | relid=0 | w=20
  725. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:familial isolated hyperparathyroidism
    n1=en:peutz-jeghers syndrome | n2=en:familial isolated hyperparathyroidism | rel=r_associated | relid=0 | w=20
  726. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:familial malignant melanoma of skin
    n1=en:peutz-jeghers syndrome | n2=en:familial malignant melanoma of skin | rel=r_associated | relid=0 | w=20
  727. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:familial median cleft of upper and lower lip
    n1=en:peutz-jeghers syndrome | n2=en:familial median cleft of upper and lower lip | rel=r_associated | relid=0 | w=20
  728. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:familial multiple myeloma
    n1=en:peutz-jeghers syndrome | n2=en:familial multiple myeloma | rel=r_associated | relid=0 | w=20
  729. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:familial multiple tumor syndrome
    n1=en:peutz-jeghers syndrome | n2=en:familial multiple tumor syndrome | rel=r_associated | relid=0 | w=20
  730. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:familial neuroblastoma
    n1=en:peutz-jeghers syndrome | n2=en:familial neuroblastoma | rel=r_associated | relid=0 | w=20
  731. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:familial non-medullary thyroid cancer
    n1=en:peutz-jeghers syndrome | n2=en:familial non-medullary thyroid cancer | rel=r_associated | relid=0 | w=20
  732. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:familial waldenstrom macroglobulinemia
    n1=en:peutz-jeghers syndrome | n2=en:familial waldenstrom macroglobulinemia | rel=r_associated | relid=0 | w=20
  733. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:fanconi anemia
    n1=en:peutz-jeghers syndrome | n2=en:fanconi anemia | rel=r_associated | relid=0 | w=20
  734. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:farber lipogranulomatosis
    n1=en:peutz-jeghers syndrome | n2=en:farber lipogranulomatosis | rel=r_associated | relid=0 | w=20
  735. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:feebleness
    n1=en:peutz-jeghers syndrome | n2=en:feebleness | rel=r_associated | relid=0 | w=20
  736. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Feingold syndrome
    n1=en:peutz-jeghers syndrome | n2=en:Feingold syndrome | rel=r_associated | relid=0 | w=20
  737. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:ferro-cerebro-cutaneous syndrome
    n1=en:peutz-jeghers syndrome | n2=en:ferro-cerebro-cutaneous syndrome | rel=r_associated | relid=0 | w=20
  738. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:fibrodysplasia ossificans progressiva
    n1=en:peutz-jeghers syndrome | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=20
  739. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:follicular atrophoderma and basal cell epitheliomata
    n1=en:peutz-jeghers syndrome | n2=en:follicular atrophoderma and basal cell epitheliomata | rel=r_associated | relid=0 | w=20
  740. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:fragile x tremor/ataxia syndrome
    n1=en:peutz-jeghers syndrome | n2=en:fragile x tremor/ataxia syndrome | rel=r_associated | relid=0 | w=20
  741. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:gastrointestinal premalignant disorders (smq)
    n1=en:peutz-jeghers syndrome | n2=en:gastrointestinal premalignant disorders (smq) | rel=r_associated | relid=0 | w=20
  742. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:generalized peeling skin syndrome
    n1=en:peutz-jeghers syndrome | n2=en:generalized peeling skin syndrome | rel=r_associated | relid=0 | w=20
  743. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:gracile bone dysplasia
    n1=en:peutz-jeghers syndrome | n2=en:gracile bone dysplasia | rel=r_associated | relid=0 | w=20
  744. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:halal syndrome
    n1=en:peutz-jeghers syndrome | n2=en:halal syndrome | rel=r_associated | relid=0 | w=20
  745. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hall riggs syndrome
    n1=en:peutz-jeghers syndrome | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=20
  746. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hamartoma of small intestine
    n1=en:peutz-jeghers syndrome | n2=en:hamartoma of small intestine | rel=r_associated | relid=0 | w=20
  747. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hashimoto-pritzker syndrome
    n1=en:peutz-jeghers syndrome | n2=en:hashimoto-pritzker syndrome | rel=r_associated | relid=0 | w=20
  748. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome
    n1=en:peutz-jeghers syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20
  749. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hereditary gastrointestinal stromal tumor
    n1=en:peutz-jeghers syndrome | n2=en:hereditary gastrointestinal stromal tumor | rel=r_associated | relid=0 | w=20
  750. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hereditary leiomyomatosis and renal cell cancer
    n1=en:peutz-jeghers syndrome | n2=en:hereditary leiomyomatosis and renal cell cancer | rel=r_associated | relid=0 | w=20
  751. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hereditary lesion
    n1=en:peutz-jeghers syndrome | n2=en:hereditary lesion | rel=r_associated | relid=0 | w=20
  752. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hereditary motor and sensory-neuropathy type ii
    n1=en:peutz-jeghers syndrome | n2=en:hereditary motor and sensory-neuropathy type ii | rel=r_associated | relid=0 | w=20
  753. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hereditary multiple ossifying ecchondromata
    n1=en:peutz-jeghers syndrome | n2=en:hereditary multiple ossifying ecchondromata | rel=r_associated | relid=0 | w=20
  754. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hereditary neoplastic syndrome
    n1=en:peutz-jeghers syndrome | n2=en:hereditary neoplastic syndrome | rel=r_associated | relid=0 | w=20
  755. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hereditary non polyposis colorectal cancer
    n1=en:peutz-jeghers syndrome | n2=en:hereditary non polyposis colorectal cancer | rel=r_associated | relid=0 | w=20
  756. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hereditary paraganglioma-pheochromocytoma syndrome
    n1=en:peutz-jeghers syndrome | n2=en:hereditary paraganglioma-pheochromocytoma syndrome | rel=r_associated | relid=0 | w=20
  757. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hereditary sensory and autonomic neuropathy type 1b
    n1=en:peutz-jeghers syndrome | n2=en:hereditary sensory and autonomic neuropathy type 1b | rel=r_associated | relid=0 | w=20
  758. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hereditary thyroid gland medullary carcinoma
    n1=en:peutz-jeghers syndrome | n2=en:hereditary thyroid gland medullary carcinoma | rel=r_associated | relid=0 | w=20
  759. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hyaline body
    n1=en:peutz-jeghers syndrome | n2=en:hyaline body | rel=r_associated | relid=0 | w=20
  760. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hyperbilirubinaemia
    n1=en:peutz-jeghers syndrome | n2=en:hyperbilirubinaemia | rel=r_associated | relid=0 | w=20
  761. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hyperinsulinism due to hnf1a deficiency
    n1=en:peutz-jeghers syndrome | n2=en:hyperinsulinism due to hnf1a deficiency | rel=r_associated | relid=0 | w=20
  762. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hyperinsulinism due to insulin receptor deficiency
    n1=en:peutz-jeghers syndrome | n2=en:hyperinsulinism due to insulin receptor deficiency | rel=r_associated | relid=0 | w=20
  763. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:peutz-jeghers syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  764. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hyperpigmented macules of buccal mucosa
    n1=en:peutz-jeghers syndrome | n2=en:hyperpigmented macules of buccal mucosa | rel=r_associated | relid=0 | w=20
  765. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hyperpigmented macules of lips
    n1=en:peutz-jeghers syndrome | n2=en:hyperpigmented macules of lips | rel=r_associated | relid=0 | w=20
  766. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hyperpigmented spots on hands (especially palms), arms, feet (especially plantar areas), legs, and lips
    n1=en:peutz-jeghers syndrome | n2=en:hyperpigmented spots on hands (especially palms), arms, feet (especially plantar areas), legs, and lips | rel=r_associated | relid=0 | w=20
  767. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hypertrichosis and acromegaloid facial appearance syndrome
    n1=en:peutz-jeghers syndrome | n2=en:hypertrichosis and acromegaloid facial appearance syndrome | rel=r_associated | relid=0 | w=20
  768. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hyperuricemia, anemia, renal failure syndrome
    n1=en:peutz-jeghers syndrome | n2=en:hyperuricemia, anemia, renal failure syndrome | rel=r_associated | relid=0 | w=20
  769. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hypohidrosis due to genetic abnormality of eccrine gland structure and function
    n1=en:peutz-jeghers syndrome | n2=en:hypohidrosis due to genetic abnormality of eccrine gland structure and function | rel=r_associated | relid=0 | w=20
  770. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:hypothalamic hamartoblastoma
    n1=en:peutz-jeghers syndrome | n2=en:hypothalamic hamartoblastoma | rel=r_associated | relid=0 | w=20
  771. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis
    n1=en:peutz-jeghers syndrome | n2=en:ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis | rel=r_associated | relid=0 | w=20
  772. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:inherited bone marrow failure syndrome
    n1=en:peutz-jeghers syndrome | n2=en:inherited bone marrow failure syndrome | rel=r_associated | relid=0 | w=20
  773. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:insulin growth factor i deficiency
    n1=en:peutz-jeghers syndrome | n2=en:insulin growth factor i deficiency | rel=r_associated | relid=0 | w=20
  774. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:intestinal hemorrhage
    n1=en:peutz-jeghers syndrome | n2=en:intestinal hemorrhage | rel=r_associated | relid=0 | w=20
  775. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:intestinal lipofuscinosis
    n1=en:peutz-jeghers syndrome | n2=en:intestinal lipofuscinosis | rel=r_associated | relid=0 | w=20
  776. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:intestinal pseudo-obstruction
    n1=en:peutz-jeghers syndrome | n2=en:intestinal pseudo-obstruction | rel=r_associated | relid=0 | w=20
  777. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:juvenile amyotrophic lateral sclerosis
    n1=en:peutz-jeghers syndrome | n2=en:juvenile amyotrophic lateral sclerosis | rel=r_associated | relid=0 | w=20
  778. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:juvenile osteochondrosis of hand
    n1=en:peutz-jeghers syndrome | n2=en:juvenile osteochondrosis of hand | rel=r_associated | relid=0 | w=20
  779. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:large intestinal polyposis
    n1=en:peutz-jeghers syndrome | n2=en:large intestinal polyposis | rel=r_associated | relid=0 | w=20
  780. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:large plaque parapsoriasis
    n1=en:peutz-jeghers syndrome | n2=en:large plaque parapsoriasis | rel=r_associated | relid=0 | w=20
  781. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:lentigo
    n1=en:peutz-jeghers syndrome | n2=en:lentigo | rel=r_associated | relid=0 | w=20
  782. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:lesion of degenerative abnormality
    n1=en:peutz-jeghers syndrome | n2=en:lesion of degenerative abnormality | rel=r_associated | relid=0 | w=20
  783. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome
    n1=en:peutz-jeghers syndrome | n2=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | rel=r_associated | relid=0 | w=20
  784. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:lissencephaly type 3 familial fetal akinesia sequence syndrome
    n1=en:peutz-jeghers syndrome | n2=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | rel=r_associated | relid=0 | w=20
  785. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:lumbosacral spondylosis without myelopathy
    n1=en:peutz-jeghers syndrome | n2=en:lumbosacral spondylosis without myelopathy | rel=r_associated | relid=0 | w=20
  786. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Lynch syndrome
    n1=en:peutz-jeghers syndrome | n2=en:Lynch syndrome | rel=r_associated | relid=0 | w=20
  787. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Lynch'syndrome
    n1=en:peutz-jeghers syndrome | n2=en:Lynch'syndrome | rel=r_associated | relid=0 | w=20
  788. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:macerated stillbirth
    n1=en:peutz-jeghers syndrome | n2=en:macerated stillbirth | rel=r_associated | relid=0 | w=20
  789. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:macies
    n1=en:peutz-jeghers syndrome | n2=en:macies | rel=r_associated | relid=0 | w=20
  790. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:major physical defect
    n1=en:peutz-jeghers syndrome | n2=en:major physical defect | rel=r_associated | relid=0 | w=20
  791. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:malignant pancreatic neoplasm
    n1=en:peutz-jeghers syndrome | n2=en:malignant pancreatic neoplasm | rel=r_associated | relid=0 | w=20
  792. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:malignant testicular germ cell tumor
    n1=en:peutz-jeghers syndrome | n2=en:malignant testicular germ cell tumor | rel=r_associated | relid=0 | w=20
  793. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:malignant thyroid gland neoplasm
    n1=en:peutz-jeghers syndrome | n2=en:malignant thyroid gland neoplasm | rel=r_associated | relid=0 | w=20
  794. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:marasmus
    n1=en:peutz-jeghers syndrome | n2=en:marasmus | rel=r_associated | relid=0 | w=20
  795. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Marfan's disease
    n1=en:peutz-jeghers syndrome | n2=en:Marfan's disease | rel=r_associated | relid=0 | w=20
  796. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Marfan's syndrome
    n1=en:peutz-jeghers syndrome | n2=en:Marfan's syndrome | rel=r_associated | relid=0 | w=20
  797. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:mccune-albright syndrome
    n1=en:peutz-jeghers syndrome | n2=en:mccune-albright syndrome | rel=r_associated | relid=0 | w=20
  798. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:McCune-Albright's syndrome
    n1=en:peutz-jeghers syndrome | n2=en:McCune-Albright's syndrome | rel=r_associated | relid=0 | w=20
  799. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:meckel diverticulum
    n1=en:peutz-jeghers syndrome | n2=en:meckel diverticulum | rel=r_associated | relid=0 | w=20
  800. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:mee's line
    n1=en:peutz-jeghers syndrome | n2=en:mee's line | rel=r_associated | relid=0 | w=20
  801. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:megalencephaly cutis marmorata telangiectatica congenita
    n1=en:peutz-jeghers syndrome | n2=en:megalencephaly cutis marmorata telangiectatica congenita | rel=r_associated | relid=0 | w=20
  802. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:melanoderma (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:melanoderma (disorder) | rel=r_associated | relid=0 | w=20
  803. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:melanodermatitis toxica lichenoides
    n1=en:peutz-jeghers syndrome | n2=en:melanodermatitis toxica lichenoides | rel=r_associated | relid=0 | w=20
  804. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome
    n1=en:peutz-jeghers syndrome | n2=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | rel=r_associated | relid=0 | w=20
  805. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome
    n1=en:peutz-jeghers syndrome | n2=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | rel=r_associated | relid=0 | w=20
  806. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:microcephaly albinism digital anomalies syndrome
    n1=en:peutz-jeghers syndrome | n2=en:microcephaly albinism digital anomalies syndrome | rel=r_associated | relid=0 | w=20
  807. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Miller's disease
    n1=en:peutz-jeghers syndrome | n2=en:Miller's disease | rel=r_associated | relid=0 | w=20
  808. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Mohr-Tranebjaerg syndrome
    n1=en:peutz-jeghers syndrome | n2=en:Mohr-Tranebjaerg syndrome | rel=r_associated | relid=0 | w=20
  809. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:morava mehes syndrome
    n1=en:peutz-jeghers syndrome | n2=en:morava mehes syndrome | rel=r_associated | relid=0 | w=20
  810. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:mosaic variegated aneuploidy
    n1=en:peutz-jeghers syndrome | n2=en:mosaic variegated aneuploidy | rel=r_associated | relid=0 | w=20
  811. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:mosaic variegated aneuploidy syndrome
    n1=en:peutz-jeghers syndrome | n2=en:mosaic variegated aneuploidy syndrome | rel=r_associated | relid=0 | w=20
  812. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:mottled pigmentation
    n1=en:peutz-jeghers syndrome | n2=en:mottled pigmentation | rel=r_associated | relid=0 | w=20
  813. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:mouth abnormalities
    n1=en:peutz-jeghers syndrome | n2=en:mouth abnormalities | rel=r_associated | relid=0 | w=20
  814. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:moyamoya disease with early onset achalasia
    n1=en:peutz-jeghers syndrome | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=20
  815. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:muir-torre syndrome
    n1=en:peutz-jeghers syndrome | n2=en:muir-torre syndrome | rel=r_associated | relid=0 | w=20
  816. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:multifocal motor neuropathy
    n1=en:peutz-jeghers syndrome | n2=en:multifocal motor neuropathy | rel=r_associated | relid=0 | w=20
  817. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:multiple endocrine neoplasia
    n1=en:peutz-jeghers syndrome | n2=en:multiple endocrine neoplasia | rel=r_associated | relid=0 | w=20
  818. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:multiple osteogenic exostoses
    n1=en:peutz-jeghers syndrome | n2=en:multiple osteogenic exostoses | rel=r_associated | relid=0 | w=20
  819. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:multiple self healing epithelioma of ferguson-smith
    n1=en:peutz-jeghers syndrome | n2=en:multiple self healing epithelioma of ferguson-smith | rel=r_associated | relid=0 | w=20
  820. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
    n1=en:peutz-jeghers syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20
  821. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:myxoid transformation of cardiac valve
    n1=en:peutz-jeghers syndrome | n2=en:myxoid transformation of cardiac valve | rel=r_associated | relid=0 | w=20
  822. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:neuronal ceroid lipofuscinosis type 3
    n1=en:peutz-jeghers syndrome | n2=en:neuronal ceroid lipofuscinosis type 3 | rel=r_associated | relid=0 | w=20
  823. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:neuronal intestinal pseudoobstruction
    n1=en:peutz-jeghers syndrome | n2=en:neuronal intestinal pseudoobstruction | rel=r_associated | relid=0 | w=20
  824. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:nevus of ota
    n1=en:peutz-jeghers syndrome | n2=en:nevus of ota | rel=r_associated | relid=0 | w=20
  825. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:nijmegen breakage syndrome
    n1=en:peutz-jeghers syndrome | n2=en:nijmegen breakage syndrome | rel=r_associated | relid=0 | w=20
  826. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Nijmegen breakage syndrome
    n1=en:peutz-jeghers syndrome | n2=en:Nijmegen breakage syndrome | rel=r_associated | relid=0 | w=20
  827. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:nystagmus
    n1=en:peutz-jeghers syndrome | n2=en:nystagmus | rel=r_associated | relid=0 | w=20
  828. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:ocular albinism-lentigines-deafness syndrome
    n1=en:peutz-jeghers syndrome | n2=en:ocular albinism-lentigines-deafness syndrome | rel=r_associated | relid=0 | w=20
  829. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:oculocerebral syndrome with hypopigmentation
    n1=en:peutz-jeghers syndrome | n2=en:oculocerebral syndrome with hypopigmentation | rel=r_associated | relid=0 | w=20
  830. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:odontoma dysphagia syndrome
    n1=en:peutz-jeghers syndrome | n2=en:odontoma dysphagia syndrome | rel=r_associated | relid=0 | w=20
  831. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:onychodystrophy
    n1=en:peutz-jeghers syndrome | n2=en:onychodystrophy | rel=r_associated | relid=0 | w=20
  832. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:ophthalmoplegia
    n1=en:peutz-jeghers syndrome | n2=en:ophthalmoplegia | rel=r_associated | relid=0 | w=20
  833. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:optic atrophy
    n1=en:peutz-jeghers syndrome | n2=en:optic atrophy | rel=r_associated | relid=0 | w=20
  834. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:osteodystrophy
    n1=en:peutz-jeghers syndrome | n2=en:osteodystrophy | rel=r_associated | relid=0 | w=20
  835. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:osteopenia
    n1=en:peutz-jeghers syndrome | n2=en:osteopenia | rel=r_associated | relid=0 | w=20
  836. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:osteous demineralization
    n1=en:peutz-jeghers syndrome | n2=en:osteous demineralization | rel=r_associated | relid=0 | w=20
  837. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:other disorders of pigmentation
    n1=en:peutz-jeghers syndrome | n2=en:other disorders of pigmentation | rel=r_associated | relid=0 | w=20
  838. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:other phakomatoses, not elsewhere classified in icd10cm
    n1=en:peutz-jeghers syndrome | n2=en:other phakomatoses, not elsewhere classified in icd10cm | rel=r_associated | relid=0 | w=20
  839. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:ovarian carcinoma
    n1=en:peutz-jeghers syndrome | n2=en:ovarian carcinoma | rel=r_associated | relid=0 | w=20
  840. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:ovarian cyst
    n1=en:peutz-jeghers syndrome | n2=en:ovarian cyst | rel=r_associated | relid=0 | w=20
  841. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome
    n1=en:peutz-jeghers syndrome | n2=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | rel=r_associated | relid=0 | w=20
  842. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:palmoplantar porokeratosis
    n1=en:peutz-jeghers syndrome | n2=en:palmoplantar porokeratosis | rel=r_associated | relid=0 | w=20
  843. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:pancreas cancer
    n1=en:peutz-jeghers syndrome | n2=en:pancreas cancer | rel=r_associated | relid=0 | w=20
  844. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:pancreatic cancer
    n1=en:peutz-jeghers syndrome | n2=en:pancreatic cancer | rel=r_associated | relid=0 | w=20
  845. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:pancreatic carcinoma
    n1=en:peutz-jeghers syndrome | n2=en:pancreatic carcinoma | rel=r_associated | relid=0 | w=20
  846. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:pancreatic neoplasm
    n1=en:peutz-jeghers syndrome | n2=en:pancreatic neoplasm | rel=r_associated | relid=0 | w=20
  847. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:papillary muscle atrophy
    n1=en:peutz-jeghers syndrome | n2=en:papillary muscle atrophy | rel=r_associated | relid=0 | w=20
  848. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:papillary muscle degeneration
    n1=en:peutz-jeghers syndrome | n2=en:papillary muscle degeneration | rel=r_associated | relid=0 | w=20
  849. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:pericarditis due to deposits of cholesterol
    n1=en:peutz-jeghers syndrome | n2=en:pericarditis due to deposits of cholesterol | rel=r_associated | relid=0 | w=20
  850. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:periorificial lentiginosis
    n1=en:peutz-jeghers syndrome | n2=en:periorificial lentiginosis | rel=r_associated | relid=0 | w=20
  851. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:peutz-jeghers polyp
    n1=en:peutz-jeghers syndrome | n2=en:peutz-jeghers polyp | rel=r_associated | relid=0 | w=20
  852. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Peutz-Jeghers syndrome
    n1=en:peutz-jeghers syndrome | n2=en:Peutz-Jeghers syndrome | rel=r_associated | relid=0 | w=20
  853. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Peutz-Jeghers' syndrome
    n1=en:peutz-jeghers syndrome | n2=en:Peutz-Jeghers' syndrome | rel=r_associated | relid=0 | w=20
  854. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Peutz-Jeghers's syndrome
    n1=en:peutz-jeghers syndrome | n2=en:Peutz-Jeghers's syndrome | rel=r_associated | relid=0 | w=20
  855. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:phakomatosis
    n1=en:peutz-jeghers syndrome | n2=en:phakomatosis | rel=r_associated | relid=0 | w=20
  856. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:phlebosclerosis
    n1=en:peutz-jeghers syndrome | n2=en:phlebosclerosis | rel=r_associated | relid=0 | w=20
  857. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:physical defect
    n1=en:peutz-jeghers syndrome | n2=en:physical defect | rel=r_associated | relid=0 | w=20
  858. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:pigment dispersion syndrome of bilateral eyes
    n1=en:peutz-jeghers syndrome | n2=en:pigment dispersion syndrome of bilateral eyes | rel=r_associated | relid=0 | w=20
  859. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:pigmentation disorder of lip
    n1=en:peutz-jeghers syndrome | n2=en:pigmentation disorder of lip | rel=r_associated | relid=0 | w=20
  860. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Pitt-Hopkins syndrome
    n1=en:peutz-jeghers syndrome | n2=en:Pitt-Hopkins syndrome | rel=r_associated | relid=0 | w=20
  861. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:pitted keratolysis
    n1=en:peutz-jeghers syndrome | n2=en:pitted keratolysis | rel=r_associated | relid=0 | w=20
  862. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:piussan lenaerts mathieu syndrome
    n1=en:peutz-jeghers syndrome | n2=en:piussan lenaerts mathieu syndrome | rel=r_associated | relid=0 | w=20
  863. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:poikiloderma, hereditary sclerosing
    n1=en:peutz-jeghers syndrome | n2=en:poikiloderma, hereditary sclerosing | rel=r_associated | relid=0 | w=20
  864. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome
    n1=en:peutz-jeghers syndrome | n2=en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome | rel=r_associated | relid=0 | w=20
  865. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:polyposis coli
    n1=en:peutz-jeghers syndrome | n2=en:polyposis coli | rel=r_associated | relid=0 | w=20
  866. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome
    n1=en:peutz-jeghers syndrome | n2=en:posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome | rel=r_associated | relid=0 | w=20
  867. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome
    n1=en:peutz-jeghers syndrome | n2=en:posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome | rel=r_associated | relid=0 | w=20
  868. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:postinflammatory hyperpigmentation
    n1=en:peutz-jeghers syndrome | n2=en:postinflammatory hyperpigmentation | rel=r_associated | relid=0 | w=20
  869. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:postinflammatory skin pigmentation change
    n1=en:peutz-jeghers syndrome | n2=en:postinflammatory skin pigmentation change | rel=r_associated | relid=0 | w=20
  870. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:potocki-shaffer syndrome
    n1=en:peutz-jeghers syndrome | n2=en:potocki-shaffer syndrome | rel=r_associated | relid=0 | w=20
  871. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:preaxial deficiency, postaxial polydactyly and hypospadias
    n1=en:peutz-jeghers syndrome | n2=en:preaxial deficiency, postaxial polydactyly and hypospadias | rel=r_associated | relid=0 | w=20
  872. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:pretematural anus
    n1=en:peutz-jeghers syndrome | n2=en:pretematural anus | rel=r_associated | relid=0 | w=20
  873. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:primary pigmented nodular adrenocortical disease
    n1=en:peutz-jeghers syndrome | n2=en:primary pigmented nodular adrenocortical disease | rel=r_associated | relid=0 | w=20
  874. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:proctatresia
    n1=en:peutz-jeghers syndrome | n2=en:proctatresia | rel=r_associated | relid=0 | w=20
  875. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:pterygium colli mental retardation digital anomalies
    n1=en:peutz-jeghers syndrome | n2=en:pterygium colli mental retardation digital anomalies | rel=r_associated | relid=0 | w=20
  876. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:pulmonary alveolar proteinosis
    n1=en:peutz-jeghers syndrome | n2=en:pulmonary alveolar proteinosis | rel=r_associated | relid=0 | w=20
  877. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome
    n1=en:peutz-jeghers syndrome | n2=en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome | rel=r_associated | relid=0 | w=20
  878. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:ras-associated autoimmune leukoproliferative disorder
    n1=en:peutz-jeghers syndrome | n2=en:ras-associated autoimmune leukoproliferative disorder | rel=r_associated | relid=0 | w=20
  879. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:rectal prolapse
    n1=en:peutz-jeghers syndrome | n2=en:rectal prolapse | rel=r_associated | relid=0 | w=20
  880. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:rhabdoid tumor predisposition syndrome
    n1=en:peutz-jeghers syndrome | n2=en:rhabdoid tumor predisposition syndrome | rel=r_associated | relid=0 | w=20
  881. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:rhinitis, atrophic
    n1=en:peutz-jeghers syndrome | n2=en:rhinitis, atrophic | rel=r_associated | relid=0 | w=20
  882. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:rothmund-thomson syndrome
    n1=en:peutz-jeghers syndrome | n2=en:rothmund-thomson syndrome | rel=r_associated | relid=0 | w=20
  883. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:schambergs disease
    n1=en:peutz-jeghers syndrome | n2=en:schambergs disease | rel=r_associated | relid=0 | w=20
  884. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:schinzel-giedion midface-retraction syndrome
    n1=en:peutz-jeghers syndrome | n2=en:schinzel-giedion midface-retraction syndrome | rel=r_associated | relid=0 | w=20
  885. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:scholte syndrome
    n1=en:peutz-jeghers syndrome | n2=en:scholte syndrome | rel=r_associated | relid=0 | w=20
  886. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:schopf-schulz-passarge syndrome (disorder)
    n1=en:peutz-jeghers syndrome | n2=en:schopf-schulz-passarge syndrome (disorder) | rel=r_associated | relid=0 | w=20
  887. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:schwannomatosis
    n1=en:peutz-jeghers syndrome | n2=en:schwannomatosis | rel=r_associated | relid=0 | w=20
  888. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:short fifth metacarpal insulin resistance syndrome
    n1=en:peutz-jeghers syndrome | n2=en:short fifth metacarpal insulin resistance syndrome | rel=r_associated | relid=0 | w=20
  889. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:skin atrophy
    n1=en:peutz-jeghers syndrome | n2=en:skin atrophy | rel=r_associated | relid=0 | w=20
  890. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:skin hypopigmentation
    n1=en:peutz-jeghers syndrome | n2=en:skin hypopigmentation | rel=r_associated | relid=0 | w=20
  891. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:solar lentigo
    n1=en:peutz-jeghers syndrome | n2=en:solar lentigo | rel=r_associated | relid=0 | w=20
  892. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Soto's syndrome
    n1=en:peutz-jeghers syndrome | n2=en:Soto's syndrome | rel=r_associated | relid=0 | w=20
  893. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:Sotos' syndrome
    n1=en:peutz-jeghers syndrome | n2=en:Sotos' syndrome | rel=r_associated | relid=0 | w=20
  894. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:sotos' syndrome
    n1=en:peutz-jeghers syndrome | n2=en:sotos' syndrome | rel=r_associated | relid=0 | w=20
  895. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:spinocerebellar ataxia type 32
    n1=en:peutz-jeghers syndrome | n2=en:spinocerebellar ataxia type 32 | rel=r_associated | relid=0 | w=20
  896. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:spinocerebellar ataxia type 37
    n1=en:peutz-jeghers syndrome | n2=en:spinocerebellar ataxia type 37 | rel=r_associated | relid=0 | w=20
  897. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:steatocystoma multiplex with natal tooth syndrome
    n1=en:peutz-jeghers syndrome | n2=en:steatocystoma multiplex with natal tooth syndrome | rel=r_associated | relid=0 | w=20
  898. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11 gene
    n1=en:peutz-jeghers syndrome | n2=en:stk11 gene | rel=r_associated | relid=0 | w=20
  899. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11 wt allele
    n1=en:peutz-jeghers syndrome | n2=en:stk11 wt allele | rel=r_associated | relid=0 | w=20
  900. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11, 1-bp del, 1407c
    n1=en:peutz-jeghers syndrome | n2=en:stk11, 1-bp del, 1407c | rel=r_associated | relid=0 | w=20
  901. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11, 1-bp del, 843g
    n1=en:peutz-jeghers syndrome | n2=en:stk11, 1-bp del, 843g | rel=r_associated | relid=0 | w=20
  902. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11, 1-bp del, 890g
    n1=en:peutz-jeghers syndrome | n2=en:stk11, 1-bp del, 890g | rel=r_associated | relid=0 | w=20
  903. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11, 1-bp ins, 535t
    n1=en:peutz-jeghers syndrome | n2=en:stk11, 1-bp ins, 535t | rel=r_associated | relid=0 | w=20
  904. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11, 2-bp del, nt277
    n1=en:peutz-jeghers syndrome | n2=en:stk11, 2-bp del, nt277 | rel=r_associated | relid=0 | w=20
  905. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11, 4-bp del, 716ggtc
    n1=en:peutz-jeghers syndrome | n2=en:stk11, 4-bp del, 716ggtc | rel=r_associated | relid=0 | w=20
  906. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11, 9-bp del
    n1=en:peutz-jeghers syndrome | n2=en:stk11, 9-bp del | rel=r_associated | relid=0 | w=20
  907. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11, ex4-5del/ex6-7inv
    n1=en:peutz-jeghers syndrome | n2=en:stk11, ex4-5del/ex6-7inv | rel=r_associated | relid=0 | w=20
  908. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11, glu57ter
    n1=en:peutz-jeghers syndrome | n2=en:stk11, glu57ter | rel=r_associated | relid=0 | w=20
  909. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11, leu67pro
    n1=en:peutz-jeghers syndrome | n2=en:stk11, leu67pro | rel=r_associated | relid=0 | w=20
  910. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11, lys84ter
    n1=en:peutz-jeghers syndrome | n2=en:stk11, lys84ter | rel=r_associated | relid=0 | w=20
  911. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11, trp239cys
    n1=en:peutz-jeghers syndrome | n2=en:stk11, trp239cys | rel=r_associated | relid=0 | w=20
  912. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11, tyr246ter
    n1=en:peutz-jeghers syndrome | n2=en:stk11, tyr246ter | rel=r_associated | relid=0 | w=20
  913. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:stk11, tyr253ter
    n1=en:peutz-jeghers syndrome | n2=en:stk11, tyr253ter | rel=r_associated | relid=0 | w=20
  914. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:teratosis
    n1=en:peutz-jeghers syndrome | n2=en:teratosis | rel=r_associated | relid=0 | w=20
  915. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:timothy syndrome type 2
    n1=en:peutz-jeghers syndrome | n2=en:timothy syndrome type 2 | rel=r_associated | relid=0 | w=20
  916. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:tophus
    n1=en:peutz-jeghers syndrome | n2=en:tophus | rel=r_associated | relid=0 | w=20
  917. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:tubular renal disease with cardiomyopathy syndrome
    n1=en:peutz-jeghers syndrome | n2=en:tubular renal disease with cardiomyopathy syndrome | rel=r_associated | relid=0 | w=20
  918. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:tylosis with esophageal cancer
    n1=en:peutz-jeghers syndrome | n2=en:tylosis with esophageal cancer | rel=r_associated | relid=0 | w=20
  919. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:type Völker-Dieben
    n1=en:peutz-jeghers syndrome | n2=en:type Völker-Dieben | rel=r_associated | relid=0 | w=20
  920. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:type Went
    n1=en:peutz-jeghers syndrome | n2=en:type Went | rel=r_associated | relid=0 | w=20
  921. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:tyrosinemia type i
    n1=en:peutz-jeghers syndrome | n2=en:tyrosinemia type i | rel=r_associated | relid=0 | w=20
  922. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:urticaria pigmentosa/maculopapular cutaneous mastocytosis
    n1=en:peutz-jeghers syndrome | n2=en:urticaria pigmentosa/maculopapular cutaneous mastocytosis | rel=r_associated | relid=0 | w=20
  923. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:von Recklinghausen's disease
    n1=en:peutz-jeghers syndrome | n2=en:von Recklinghausen's disease | rel=r_associated | relid=0 | w=20
  924. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:vulval melanotic macule
    n1=en:peutz-jeghers syndrome | n2=en:vulval melanotic macule | rel=r_associated | relid=0 | w=20
  925. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:vulvar dystrophy
    n1=en:peutz-jeghers syndrome | n2=en:vulvar dystrophy | rel=r_associated | relid=0 | w=20
  926. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome
    n1=en:peutz-jeghers syndrome | n2=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome | rel=r_associated | relid=0 | w=20
  927. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:wilms tumor-aniridia-genitourinary anomalies-mental retardation-obesity syndrome
    n1=en:peutz-jeghers syndrome | n2=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation-obesity syndrome | rel=r_associated | relid=0 | w=20
  928. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:wyburn mason's syndrome
    n1=en:peutz-jeghers syndrome | n2=en:wyburn mason's syndrome | rel=r_associated | relid=0 | w=20
  929. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:X-linked
    n1=en:peutz-jeghers syndrome | n2=en:X-linked | rel=r_associated | relid=0 | w=20
  930. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:x-linked intellectual disability with acromegaly and hyperactivity syndrome
    n1=en:peutz-jeghers syndrome | n2=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | rel=r_associated | relid=0 | w=20
  931. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:x-linked intellectual disability with ataxia and apraxia syndrome
    n1=en:peutz-jeghers syndrome | n2=en:x-linked intellectual disability with ataxia and apraxia syndrome | rel=r_associated | relid=0 | w=20
  932. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome
    n1=en:peutz-jeghers syndrome | n2=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | rel=r_associated | relid=0 | w=20
  933. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:xanthoma of lung
    n1=en:peutz-jeghers syndrome | n2=en:xanthoma of lung | rel=r_associated | relid=0 | w=20
  934. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:yellow nail syndrome
    n1=en:peutz-jeghers syndrome | n2=en:yellow nail syndrome | rel=r_associated | relid=0 | w=20
  935. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:yemenite deaf-blind hypopigmentation syndrome
    n1=en:peutz-jeghers syndrome | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=20
  936. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> en:zinc-deficiency type
    n1=en:peutz-jeghers syndrome | n2=en:zinc-deficiency type | rel=r_associated | relid=0 | w=20
  937. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> envie
    n1=en:peutz-jeghers syndrome | n2=envie | rel=r_associated | relid=0 | w=20
  938. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> enzymologie
    n1=en:peutz-jeghers syndrome | n2=enzymologie | rel=r_associated | relid=0 | w=20
  939. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> enzymology
    n1=en:peutz-jeghers syndrome | n2=enzymology | rel=r_associated | relid=0 | w=20
  940. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> épidémiologique
    n1=en:peutz-jeghers syndrome | n2=épidémiologique | rel=r_associated | relid=0 | w=20
  941. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> épidermolyse bulleuse acquise
    n1=en:peutz-jeghers syndrome | n2=épidermolyse bulleuse acquise | rel=r_associated | relid=0 | w=20
  942. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Épidermolyse bulleuse acquise
    n1=en:peutz-jeghers syndrome | n2=Épidermolyse bulleuse acquise | rel=r_associated | relid=0 | w=20
  943. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> état criblé
    n1=en:peutz-jeghers syndrome | n2=état criblé | rel=r_associated | relid=0 | w=20
  944. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> ethnologique
    n1=en:peutz-jeghers syndrome | n2=ethnologique | rel=r_associated | relid=0 | w=20
  945. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> exostosante (maladie)
    n1=en:peutz-jeghers syndrome | n2=exostosante (maladie) | rel=r_associated | relid=0 | w=20
  946. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> exostose héréditaire multiple
    n1=en:peutz-jeghers syndrome | n2=exostose héréditaire multiple | rel=r_associated | relid=0 | w=20
  947. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> fibromatose gingivale
    n1=en:peutz-jeghers syndrome | n2=fibromatose gingivale | rel=r_associated | relid=0 | w=20
  948. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> gastroentérologie
    n1=en:peutz-jeghers syndrome | n2=gastroentérologie | rel=r_associated | relid=0 | w=20
  949. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> gène LKB1
    n1=en:peutz-jeghers syndrome | n2=gène LKB1 | rel=r_associated | relid=0 | w=20
  950. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> génétique
    n1=en:peutz-jeghers syndrome | n2=génétique | rel=r_associated | relid=0 | w=20
  951. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> gigantisme cérébral
    n1=en:peutz-jeghers syndrome | n2=gigantisme cérébral | rel=r_associated | relid=0 | w=20
  952. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> goniodysgénésie-retard mental-petite taille (syndrome)
    n1=en:peutz-jeghers syndrome | n2=goniodysgénésie-retard mental-petite taille (syndrome) | rel=r_associated | relid=0 | w=20
  953. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> gynécomastie
    n1=en:peutz-jeghers syndrome | n2=gynécomastie | rel=r_associated | relid=0 | w=20
  954. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale
    n1=en:peutz-jeghers syndrome | n2=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | rel=r_associated | relid=0 | w=20
  955. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> hamartome
    n1=en:peutz-jeghers syndrome | n2=hamartome | rel=r_associated | relid=0 | w=20
  956. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> hyperbilirubinémie
    n1=en:peutz-jeghers syndrome | n2=hyperbilirubinémie | rel=r_associated | relid=0 | w=20
  957. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> hyperpigmentation
    n1=en:peutz-jeghers syndrome | n2=hyperpigmentation | rel=r_associated | relid=0 | w=20
  958. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> ichthyose congénitale
    n1=en:peutz-jeghers syndrome | n2=ichthyose congénitale | rel=r_associated | relid=0 | w=20
  959. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> ictère nucléaire
    n1=en:peutz-jeghers syndrome | n2=ictère nucléaire | rel=r_associated | relid=0 | w=20
  960. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> imperforation anale
    n1=en:peutz-jeghers syndrome | n2=imperforation anale | rel=r_associated | relid=0 | w=20
  961. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> imperforation de l'anus
    n1=en:peutz-jeghers syndrome | n2=imperforation de l'anus | rel=r_associated | relid=0 | w=20
  962. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Jeghers
    n1=en:peutz-jeghers syndrome | n2=Jeghers | rel=r_associated | relid=0 | w=20
  963. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> kératolyse ponctuée
    n1=en:peutz-jeghers syndrome | n2=kératolyse ponctuée | rel=r_associated | relid=0 | w=20
  964. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Kjer (atrophie optique de type)
    n1=en:peutz-jeghers syndrome | n2=Kjer (atrophie optique de type) | rel=r_associated | relid=0 | w=20
  965. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> kyste à l'ovaire
    n1=en:peutz-jeghers syndrome | n2=kyste à l'ovaire | rel=r_associated | relid=0 | w=20
  966. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> kyste de l'ovaire
    n1=en:peutz-jeghers syndrome | n2=kyste de l'ovaire | rel=r_associated | relid=0 | w=20
  967. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> kyste ovarien
    n1=en:peutz-jeghers syndrome | n2=kyste ovarien | rel=r_associated | relid=0 | w=20
  968. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> kyste ovarien bénin
    n1=en:peutz-jeghers syndrome | n2=kyste ovarien bénin | rel=r_associated | relid=0 | w=20
  969. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> kyste rétentionnel de l'ovaire
    n1=en:peutz-jeghers syndrome | n2=kyste rétentionnel de l'ovaire | rel=r_associated | relid=0 | w=20
  970. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> laparotomie
    n1=en:peutz-jeghers syndrome | n2=laparotomie | rel=r_associated | relid=0 | w=20
  971. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> lentiginose péri-orificielle
    n1=en:peutz-jeghers syndrome | n2=lentiginose péri-orificielle | rel=r_associated | relid=0 | w=20
  972. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> lipofuscinose neuronale céroïde
    n1=en:peutz-jeghers syndrome | n2=lipofuscinose neuronale céroïde | rel=r_associated | relid=0 | w=20
  973. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> lipofuscinose neuronale céroïde infantile finlandaise
    n1=en:peutz-jeghers syndrome | n2=lipofuscinose neuronale céroïde infantile finlandaise | rel=r_associated | relid=0 | w=20
  974. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> lung
    n1=en:peutz-jeghers syndrome | n2=lung | rel=r_associated | relid=0 | w=20
  975. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie
    n1=en:peutz-jeghers syndrome | n2=maladie | rel=r_associated | relid=0 | w=20
  976. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie clinique de recklinghausen
    n1=en:peutz-jeghers syndrome | n2=maladie clinique de recklinghausen | rel=r_associated | relid=0 | w=20
  977. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie congénitale
    n1=en:peutz-jeghers syndrome | n2=maladie congénitale | rel=r_associated | relid=0 | w=20
  978. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie de Bessel-Hagen
    n1=en:peutz-jeghers syndrome | n2=maladie de Bessel-Hagen | rel=r_associated | relid=0 | w=20
  979. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie de l'appareil digestif
    n1=en:peutz-jeghers syndrome | n2=maladie de l'appareil digestif | rel=r_associated | relid=0 | w=20
  980. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie de la peau
    n1=en:peutz-jeghers syndrome | n2=maladie de la peau | rel=r_associated | relid=0 | w=20
  981. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie de marfan
    n1=en:peutz-jeghers syndrome | n2=maladie de marfan | rel=r_associated | relid=0 | w=20
  982. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie de Recklinghausen
    n1=en:peutz-jeghers syndrome | n2=maladie de Recklinghausen | rel=r_associated | relid=0 | w=20
  983. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie de von Recklinghausen
    n1=en:peutz-jeghers syndrome | n2=maladie de von Recklinghausen | rel=r_associated | relid=0 | w=20
  984. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie des exostoses multiples
    n1=en:peutz-jeghers syndrome | n2=maladie des exostoses multiples | rel=r_associated | relid=0 | w=20
  985. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie exostosante multiple
    n1=en:peutz-jeghers syndrome | n2=maladie exostosante multiple | rel=r_associated | relid=0 | w=20
  986. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie gastro-intestinale
    n1=en:peutz-jeghers syndrome | n2=maladie gastro-intestinale | rel=r_associated | relid=0 | w=20
  987. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie génétique
    n1=en:peutz-jeghers syndrome | n2=maladie génétique | rel=r_associated | relid=0 | w=20
  988. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie intestinale
    n1=en:peutz-jeghers syndrome | n2=maladie intestinale | rel=r_associated | relid=0 | w=20
  989. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie neurodégénérative du système nerveux central
    n1=en:peutz-jeghers syndrome | n2=maladie neurodégénérative du système nerveux central | rel=r_associated | relid=0 | w=20
  990. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie ostéogénique
    n1=en:peutz-jeghers syndrome | n2=maladie ostéogénique | rel=r_associated | relid=0 | w=20
  991. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie rare
    n1=en:peutz-jeghers syndrome | n2=maladie rare | rel=r_associated | relid=0 | w=20
  992. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladie
    (médecine)
    n1=en:peutz-jeghers syndrome | n2=maladie
    (médecine)
    | rel=r_associated | relid=0 | w=20
  993. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> maladies
    n1=en:peutz-jeghers syndrome | n2=maladies | rel=r_associated | relid=0 | w=20
  994. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> malformation congénitale
    n1=en:peutz-jeghers syndrome | n2=malformation congénitale | rel=r_associated | relid=0 | w=20
  995. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> malformations buccales
    n1=en:peutz-jeghers syndrome | n2=malformations buccales | rel=r_associated | relid=0 | w=20
  996. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> malformations de la bouche
    n1=en:peutz-jeghers syndrome | n2=malformations de la bouche | rel=r_associated | relid=0 | w=20
  997. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Médecine
    n1=en:peutz-jeghers syndrome | n2=Médecine | rel=r_associated | relid=0 | w=20
  998. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> médecine
    n1=en:peutz-jeghers syndrome | n2=médecine | rel=r_associated | relid=0 | w=20
  999. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> médecine spécialisée
    n1=en:peutz-jeghers syndrome | n2=médecine spécialisée | rel=r_associated | relid=0 | w=20
  1000. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> médecine
    (science)
    n1=en:peutz-jeghers syndrome | n2=médecine
    (science)
    | rel=r_associated | relid=0 | w=20
  1001. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> mélanodermite toxique
    n1=en:peutz-jeghers syndrome | n2=mélanodermite toxique | rel=r_associated | relid=0 | w=20
  1002. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> mélanodermite toxique d'Hoffmann-Habermann
    n1=en:peutz-jeghers syndrome | n2=mélanodermite toxique d'Hoffmann-Habermann | rel=r_associated | relid=0 | w=20
  1003. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> mélanose
    n1=en:peutz-jeghers syndrome | n2=mélanose | rel=r_associated | relid=0 | w=20
  1004. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> mélanose
    (médecine)
    n1=en:peutz-jeghers syndrome | n2=mélanose
    (médecine)
    | rel=r_associated | relid=0 | w=20
  1005. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> mélasma
    n1=en:peutz-jeghers syndrome | n2=mélasma | rel=r_associated | relid=0 | w=20
  1006. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> microbiologique
    n1=en:peutz-jeghers syndrome | n2=microbiologique | rel=r_associated | relid=0 | w=20
  1007. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> microdélétion 5q35
    n1=en:peutz-jeghers syndrome | n2=microdélétion 5q35 | rel=r_associated | relid=0 | w=20
  1008. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> migraine hémiplégique familiale
    n1=en:peutz-jeghers syndrome | n2=migraine hémiplégique familiale | rel=r_associated | relid=0 | w=20
  1009. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> muqueuse
    n1=en:peutz-jeghers syndrome | n2=muqueuse | rel=r_associated | relid=0 | w=20
  1010. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> naevomatose baso-cellulaire
    n1=en:peutz-jeghers syndrome | n2=naevomatose baso-cellulaire | rel=r_associated | relid=0 | w=20
  1011. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> naevomatose basocellulaire
    n1=en:peutz-jeghers syndrome | n2=naevomatose basocellulaire | rel=r_associated | relid=0 | w=20
  1012. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> naevus - voir index alphabétique
    n1=en:peutz-jeghers syndrome | n2=naevus - voir index alphabétique | rel=r_associated | relid=0 | w=20
  1013. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> nævomatose basocellulaire multiple
    n1=en:peutz-jeghers syndrome | n2=nævomatose basocellulaire multiple | rel=r_associated | relid=0 | w=20
  1014. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> nævus dysplasique (syndrome du)
    n1=en:peutz-jeghers syndrome | n2=nævus dysplasique (syndrome du) | rel=r_associated | relid=0 | w=20
  1015. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> NEM 2B ou 3
    n1=en:peutz-jeghers syndrome | n2=NEM 2B ou 3 | rel=r_associated | relid=0 | w=20
  1016. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> néoplasie endocrinienne multiple (MEN 2B ou 3)
    n1=en:peutz-jeghers syndrome | n2=néoplasie endocrinienne multiple (MEN 2B ou 3) | rel=r_associated | relid=0 | w=20
  1017. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> néoplasie gastro-intestinale
    n1=en:peutz-jeghers syndrome | n2=néoplasie gastro-intestinale | rel=r_associated | relid=0 | w=20
  1018. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> neurofibromatose
    n1=en:peutz-jeghers syndrome | n2=neurofibromatose | rel=r_associated | relid=0 | w=20
  1019. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> neurofibromatose de Recklinghausen
    n1=en:peutz-jeghers syndrome | n2=neurofibromatose de Recklinghausen | rel=r_associated | relid=0 | w=20
  1020. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> neurofibromatose de recklinghausen
    n1=en:peutz-jeghers syndrome | n2=neurofibromatose de recklinghausen | rel=r_associated | relid=0 | w=20
  1021. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> neurofibromatose de type 1
    n1=en:peutz-jeghers syndrome | n2=neurofibromatose de type 1 | rel=r_associated | relid=0 | w=20
  1022. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> neurofibromatose de type périphérique
    n1=en:peutz-jeghers syndrome | n2=neurofibromatose de type périphérique | rel=r_associated | relid=0 | w=20
  1023. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> neurofibromatose de type VI
    n1=en:peutz-jeghers syndrome | n2=neurofibromatose de type VI | rel=r_associated | relid=0 | w=20
  1024. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> neuropathie héréditaire sensitive et autonome de type 1
    n1=en:peutz-jeghers syndrome | n2=neuropathie héréditaire sensitive et autonome de type 1 | rel=r_associated | relid=0 | w=20
  1025. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> neuropathie héréditaire sensitive et autonome de type i
    n1=en:peutz-jeghers syndrome | n2=neuropathie héréditaire sensitive et autonome de type i | rel=r_associated | relid=0 | w=20
  1026. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> neuropathie motrice multifocale
    n1=en:peutz-jeghers syndrome | n2=neuropathie motrice multifocale | rel=r_associated | relid=0 | w=20
  1027. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> neuropathie sensitive héréditaire dominante de type i
    n1=en:peutz-jeghers syndrome | n2=neuropathie sensitive héréditaire dominante de type i | rel=r_associated | relid=0 | w=20
  1028. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> neuropathie sensitive héréditaire dominante de type I
    n1=en:peutz-jeghers syndrome | n2=neuropathie sensitive héréditaire dominante de type I | rel=r_associated | relid=0 | w=20
  1029. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> neuropathie tropicale ataxique
    n1=en:peutz-jeghers syndrome | n2=neuropathie tropicale ataxique | rel=r_associated | relid=0 | w=20
  1030. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> nystagmus
    n1=en:peutz-jeghers syndrome | n2=nystagmus | rel=r_associated | relid=0 | w=20
  1031. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> nystagmus congénital isolé
    n1=en:peutz-jeghers syndrome | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
  1032. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> nystagmus lié au sexe
    n1=en:peutz-jeghers syndrome | n2=nystagmus lié au sexe | rel=r_associated | relid=0 | w=20
  1033. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> occlusion intestinale
    n1=en:peutz-jeghers syndrome | n2=occlusion intestinale | rel=r_associated | relid=0 | w=20
  1034. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> oculo-cérébral avec hypopigmentation (syndrome)
    n1=en:peutz-jeghers syndrome | n2=oculo-cérébral avec hypopigmentation (syndrome) | rel=r_associated | relid=0 | w=20
  1035. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> oestrogène
    n1=en:peutz-jeghers syndrome | n2=oestrogène | rel=r_associated | relid=0 | w=20
  1036. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> oncologie
    n1=en:peutz-jeghers syndrome | n2=oncologie | rel=r_associated | relid=0 | w=20
  1037. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> ongles jaunes (syndrome des)
    n1=en:peutz-jeghers syndrome | n2=ongles jaunes (syndrome des) | rel=r_associated | relid=0 | w=20
  1038. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> onycho-ostéodysostose
    n1=en:peutz-jeghers syndrome | n2=onycho-ostéodysostose | rel=r_associated | relid=0 | w=20
  1039. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> onycho-patellaire (syndrome)
    n1=en:peutz-jeghers syndrome | n2=onycho-patellaire (syndrome) | rel=r_associated | relid=0 | w=20
  1040. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> onychodystrophie
    n1=en:peutz-jeghers syndrome | n2=onychodystrophie | rel=r_associated | relid=0 | w=20
  1041. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> ostéodystrophie
    n1=en:peutz-jeghers syndrome | n2=ostéodystrophie | rel=r_associated | relid=0 | w=20
  1042. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> ostéolyse
    n1=en:peutz-jeghers syndrome | n2=ostéolyse | rel=r_associated | relid=0 | w=20
  1043. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> ostéomalacie
    n1=en:peutz-jeghers syndrome | n2=ostéomalacie | rel=r_associated | relid=0 | w=20
  1044. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> ostéopénie
    n1=en:peutz-jeghers syndrome | n2=ostéopénie | rel=r_associated | relid=0 | w=20
  1045. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> pancréas (cancer du)
    n1=en:peutz-jeghers syndrome | n2=pancréas (cancer du) | rel=r_associated | relid=0 | w=20
  1046. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> papule
    n1=en:peutz-jeghers syndrome | n2=papule | rel=r_associated | relid=0 | w=20
  1047. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> papule
    (médecine)
    n1=en:peutz-jeghers syndrome | n2=papule
    (médecine)
    | rel=r_associated | relid=0 | w=20
  1048. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> paraplégie spastique avec atrophie optique et démence
    n1=en:peutz-jeghers syndrome | n2=paraplégie spastique avec atrophie optique et démence | rel=r_associated | relid=0 | w=20
  1049. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> parasitologie
    n1=en:peutz-jeghers syndrome | n2=parasitologie | rel=r_associated | relid=0 | w=20
  1050. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> partie non précisée tumeur maligne du pancréas
    n1=en:peutz-jeghers syndrome | n2=partie non précisée tumeur maligne du pancréas | rel=r_associated | relid=0 | w=20
  1051. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> pathologie congénitale
    n1=en:peutz-jeghers syndrome | n2=pathologie congénitale | rel=r_associated | relid=0 | w=20
  1052. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> peau
    n1=en:peutz-jeghers syndrome | n2=peau | rel=r_associated | relid=0 | w=20
  1053. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> peau
    (anatomie)
    n1=en:peutz-jeghers syndrome | n2=peau
    (anatomie)
    | rel=r_associated | relid=0 | w=20
  1054. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Peutz
    n1=en:peutz-jeghers syndrome | n2=Peutz | rel=r_associated | relid=0 | w=20
  1055. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Peutz-Jeghers (syndrome de)
    n1=en:peutz-jeghers syndrome | n2=Peutz-Jeghers (syndrome de) | rel=r_associated | relid=0 | w=20
  1056. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> phlébosclérose
    n1=en:peutz-jeghers syndrome | n2=phlébosclérose | rel=r_associated | relid=0 | w=20
  1057. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> piébaldisme
    n1=en:peutz-jeghers syndrome | n2=piébaldisme | rel=r_associated | relid=0 | w=20
  1058. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> piebaldisme
    n1=en:peutz-jeghers syndrome | n2=piebaldisme | rel=r_associated | relid=0 | w=20
  1059. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> poïkilodermatomyosite de Petges et Cléjat
    n1=en:peutz-jeghers syndrome | n2=poïkilodermatomyosite de Petges et Cléjat | rel=r_associated | relid=0 | w=20
  1060. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> polype
    n1=en:peutz-jeghers syndrome | n2=polype | rel=r_associated | relid=0 | w=20
  1061. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> polype
    (médecine)
    n1=en:peutz-jeghers syndrome | n2=polype
    (médecine)
    | rel=r_associated | relid=0 | w=20
  1062. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> polypose adénomateuse familiale
    n1=en:peutz-jeghers syndrome | n2=polypose adénomateuse familiale | rel=r_associated | relid=0 | w=20
  1063. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> polypose colique familiale
    n1=en:peutz-jeghers syndrome | n2=polypose colique familiale | rel=r_associated | relid=0 | w=20
  1064. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> polypose recto-colique familiale
    n1=en:peutz-jeghers syndrome | n2=polypose recto-colique familiale | rel=r_associated | relid=0 | w=20
  1065. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> polypose rectocolique
    n1=en:peutz-jeghers syndrome | n2=polypose rectocolique | rel=r_associated | relid=0 | w=20
  1066. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> polypose rectocolique familiale
    n1=en:peutz-jeghers syndrome | n2=polypose rectocolique familiale | rel=r_associated | relid=0 | w=20
  1067. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> polypose rhino-sinusienne déformante
    n1=en:peutz-jeghers syndrome | n2=polypose rhino-sinusienne déformante | rel=r_associated | relid=0 | w=20
  1068. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> poumon vert
    n1=en:peutz-jeghers syndrome | n2=poumon vert | rel=r_associated | relid=0 | w=20
  1069. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> processus pathologique
    n1=en:peutz-jeghers syndrome | n2=processus pathologique | rel=r_associated | relid=0 | w=20
  1070. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> prolapsus de la muqueuse rectale
    n1=en:peutz-jeghers syndrome | n2=prolapsus de la muqueuse rectale | rel=r_associated | relid=0 | w=20
  1071. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> prolapsus du rectum
    n1=en:peutz-jeghers syndrome | n2=prolapsus du rectum | rel=r_associated | relid=0 | w=20
  1072. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> prolapsus rectal
    n1=en:peutz-jeghers syndrome | n2=prolapsus rectal | rel=r_associated | relid=0 | w=20
  1073. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Prolapsus rectal
    n1=en:peutz-jeghers syndrome | n2=Prolapsus rectal | rel=r_associated | relid=0 | w=20
  1074. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> protéinose alvéolaire
    n1=en:peutz-jeghers syndrome | n2=protéinose alvéolaire | rel=r_associated | relid=0 | w=20
  1075. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> protéinose alvéolaire pulmonaire
    n1=en:peutz-jeghers syndrome | n2=protéinose alvéolaire pulmonaire | rel=r_associated | relid=0 | w=20
  1076. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> radiographique
    n1=en:peutz-jeghers syndrome | n2=radiographique | rel=r_associated | relid=0 | w=20
  1077. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Recklinghausen (maladie de von)
    n1=en:peutz-jeghers syndrome | n2=Recklinghausen (maladie de von) | rel=r_associated | relid=0 | w=20
  1078. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Recklinghausen (neurofibromatose de)
    n1=en:peutz-jeghers syndrome | n2=Recklinghausen (neurofibromatose de) | rel=r_associated | relid=0 | w=20
  1079. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Rendu-Osler (angiomatose hémorragique héréditaire ou familiale de)
    n1=en:peutz-jeghers syndrome | n2=Rendu-Osler (angiomatose hémorragique héréditaire ou familiale de) | rel=r_associated | relid=0 | w=20
  1080. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> retard mental, retard de croissance, surdité, microgénitalisme lié au sexe
    n1=en:peutz-jeghers syndrome | n2=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | rel=r_associated | relid=0 | w=20
  1081. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> rhabdomyolyse
    n1=en:peutz-jeghers syndrome | n2=rhabdomyolyse | rel=r_associated | relid=0 | w=20
  1082. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> sclérose artérielle
    n1=en:peutz-jeghers syndrome | n2=sclérose artérielle | rel=r_associated | relid=0 | w=20
  1083. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> sclérose des artères
    n1=en:peutz-jeghers syndrome | n2=sclérose des artères | rel=r_associated | relid=0 | w=20
  1084. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> sclérose tubéreuse du cerveau
    n1=en:peutz-jeghers syndrome | n2=sclérose tubéreuse du cerveau | rel=r_associated | relid=0 | w=20
  1085. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Sotos (syndrome de)
    n1=en:peutz-jeghers syndrome | n2=Sotos (syndrome de) | rel=r_associated | relid=0 | w=20
  1086. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> spécialités médicales
    n1=en:peutz-jeghers syndrome | n2=spécialités médicales | rel=r_associated | relid=0 | w=20
  1087. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> stéatohépatite
    n1=en:peutz-jeghers syndrome | n2=stéatohépatite | rel=r_associated | relid=0 | w=20
  1088. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> STK11 gene
    n1=en:peutz-jeghers syndrome | n2=STK11 gene | rel=r_associated | relid=0 | w=20
  1089. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> stomatocytose héréditaire
    n1=en:peutz-jeghers syndrome | n2=stomatocytose héréditaire | rel=r_associated | relid=0 | w=20
  1090. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome d'Alagille
    n1=en:peutz-jeghers syndrome | n2=syndrome d'Alagille | rel=r_associated | relid=0 | w=20
  1091. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome d'alagille
    n1=en:peutz-jeghers syndrome | n2=syndrome d'alagille | rel=r_associated | relid=0 | w=20
  1092. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de
    n1=en:peutz-jeghers syndrome | n2=syndrome de | rel=r_associated | relid=0 | w=20
  1093. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de douleur extrême paroxystique
    n1=en:peutz-jeghers syndrome | n2=syndrome de douleur extrême paroxystique | rel=r_associated | relid=0 | w=20
  1094. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de dubin-johnson
    n1=en:peutz-jeghers syndrome | n2=syndrome de dubin-johnson | rel=r_associated | relid=0 | w=20
  1095. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de Dubin-Johnson
    n1=en:peutz-jeghers syndrome | n2=syndrome de Dubin-Johnson | rel=r_associated | relid=0 | w=20
  1096. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de Gorlin
    n1=en:peutz-jeghers syndrome | n2=syndrome de Gorlin | rel=r_associated | relid=0 | w=20
  1097. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de gorlin
    n1=en:peutz-jeghers syndrome | n2=syndrome de gorlin | rel=r_associated | relid=0 | w=20
  1098. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de Lynch
    n1=en:peutz-jeghers syndrome | n2=syndrome de Lynch | rel=r_associated | relid=0 | w=20
  1099. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de marfan
    n1=en:peutz-jeghers syndrome | n2=syndrome de marfan | rel=r_associated | relid=0 | w=20
  1100. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de McCune-Albright
    n1=en:peutz-jeghers syndrome | n2=syndrome de McCune-Albright | rel=r_associated | relid=0 | w=20
  1101. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de Peutz-Touraine-Jeghers
    n1=en:peutz-jeghers syndrome | n2=syndrome de Peutz-Touraine-Jeghers | rel=r_associated | relid=0 | w=20
  1102. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire
    n1=en:peutz-jeghers syndrome | n2=syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire | rel=r_associated | relid=0 | w=20
  1103. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Syndrome de prédisposition héréditaire aux adénocarcinomes pancréatiques
    n1=en:peutz-jeghers syndrome | n2=Syndrome de prédisposition héréditaire aux adénocarcinomes pancréatiques | rel=r_associated | relid=0 | w=20
  1104. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de soto
    n1=en:peutz-jeghers syndrome | n2=syndrome de soto | rel=r_associated | relid=0 | w=20
  1105. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de Sotos
    n1=en:peutz-jeghers syndrome | n2=syndrome de Sotos | rel=r_associated | relid=0 | w=20
  1106. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de sotos
    n1=en:peutz-jeghers syndrome | n2=syndrome de sotos | rel=r_associated | relid=0 | w=20
  1107. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome de Treft-Sanborn-Carey
    n1=en:peutz-jeghers syndrome | n2=syndrome de Treft-Sanborn-Carey | rel=r_associated | relid=0 | w=20
  1108. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome héréditaire de cancer du sein et de l'ovaire
    n1=en:peutz-jeghers syndrome | n2=syndrome héréditaire de cancer du sein et de l'ovaire | rel=r_associated | relid=0 | w=20
  1109. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire
    n1=en:peutz-jeghers syndrome | n2=syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire | rel=r_associated | relid=0 | w=20
  1110. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> syndrome oculo-cérébral avec hypopigmentation
    n1=en:peutz-jeghers syndrome | n2=syndrome oculo-cérébral avec hypopigmentation | rel=r_associated | relid=0 | w=20
  1111. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tare congénitale
    n1=en:peutz-jeghers syndrome | n2=tare congénitale | rel=r_associated | relid=0 | w=20
  1112. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> télangiectasie hémorragique héréditaire
    n1=en:peutz-jeghers syndrome | n2=télangiectasie hémorragique héréditaire | rel=r_associated | relid=0 | w=20
  1113. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> testicule
    n1=en:peutz-jeghers syndrome | n2=testicule | rel=r_associated | relid=0 | w=20
  1114. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tophus
    n1=en:peutz-jeghers syndrome | n2=tophus | rel=r_associated | relid=0 | w=20
  1115. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tophus goutteux
    n1=en:peutz-jeghers syndrome | n2=tophus goutteux | rel=r_associated | relid=0 | w=20
  1116. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> transmission autosomique dominante
    n1=en:peutz-jeghers syndrome | n2=transmission autosomique dominante | rel=r_associated | relid=0 | w=20
  1117. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tumeur bénigne du pancréas
    n1=en:peutz-jeghers syndrome | n2=tumeur bénigne du pancréas | rel=r_associated | relid=0 | w=20
  1118. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tumeur bénigne pancréatique
    n1=en:peutz-jeghers syndrome | n2=tumeur bénigne pancréatique | rel=r_associated | relid=0 | w=20
  1119. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tumeur du pancréas
    n1=en:peutz-jeghers syndrome | n2=tumeur du pancréas | rel=r_associated | relid=0 | w=20
  1120. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tumeur gastro-intestinale
    n1=en:peutz-jeghers syndrome | n2=tumeur gastro-intestinale | rel=r_associated | relid=0 | w=20
  1121. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tumeur gastrointestinale
    n1=en:peutz-jeghers syndrome | n2=tumeur gastrointestinale | rel=r_associated | relid=0 | w=20
  1122. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tumeur maligne du pancréas
    n1=en:peutz-jeghers syndrome | n2=tumeur maligne du pancréas | rel=r_associated | relid=0 | w=20
  1123. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tumeur maligne pancréatique
    n1=en:peutz-jeghers syndrome | n2=tumeur maligne pancréatique | rel=r_associated | relid=0 | w=20
  1124. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tumeur pancréatique maligne
    n1=en:peutz-jeghers syndrome | n2=tumeur pancréatique maligne | rel=r_associated | relid=0 | w=20
  1125. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tumeurs du pancréas
    n1=en:peutz-jeghers syndrome | n2=tumeurs du pancréas | rel=r_associated | relid=0 | w=20
  1126. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tumeurs du pancreas
    n1=en:peutz-jeghers syndrome | n2=tumeurs du pancreas | rel=r_associated | relid=0 | w=20
  1127. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tumeurs pancréatiques
    n1=en:peutz-jeghers syndrome | n2=tumeurs pancréatiques | rel=r_associated | relid=0 | w=20
  1128. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> tylosis
    n1=en:peutz-jeghers syndrome | n2=tylosis | rel=r_associated | relid=0 | w=20
  1129. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> une anomalie congénitale
    n1=en:peutz-jeghers syndrome | n2=une anomalie congénitale | rel=r_associated | relid=0 | w=20
  1130. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> van Bogaert (xanthomatose cérébrotendineuse de)
    n1=en:peutz-jeghers syndrome | n2=van Bogaert (xanthomatose cérébrotendineuse de) | rel=r_associated | relid=0 | w=20
  1131. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> vestige du conduit vitellin
    n1=en:peutz-jeghers syndrome | n2=vestige du conduit vitellin | rel=r_associated | relid=0 | w=20
  1132. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> vice de conformation
    n1=en:peutz-jeghers syndrome | n2=vice de conformation | rel=r_associated | relid=0 | w=20
  1133. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Völker-Dieben (atrophie optique liée au sexe de)
    n1=en:peutz-jeghers syndrome | n2=Völker-Dieben (atrophie optique liée au sexe de) | rel=r_associated | relid=0 | w=20
  1134. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Walker-Warburg (syndrome de)
    n1=en:peutz-jeghers syndrome | n2=Walker-Warburg (syndrome de) | rel=r_associated | relid=0 | w=20
  1135. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Warburg
    n1=en:peutz-jeghers syndrome | n2=Warburg | rel=r_associated | relid=0 | w=20
  1136. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Went (atrophie optique liée au sexe de)
    n1=en:peutz-jeghers syndrome | n2=Went (atrophie optique liée au sexe de) | rel=r_associated | relid=0 | w=20
  1137. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> xanthomatose cérébro-tendineuse
    n1=en:peutz-jeghers syndrome | n2=xanthomatose cérébro-tendineuse | rel=r_associated | relid=0 | w=20
  1138. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> xanthomatose cérébrotendineuse
    n1=en:peutz-jeghers syndrome | n2=xanthomatose cérébrotendineuse | rel=r_associated | relid=0 | w=20
  1139. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> xanthomatose cérébrotendineuse de Van Bogaert
    n1=en:peutz-jeghers syndrome | n2=xanthomatose cérébrotendineuse de Van Bogaert | rel=r_associated | relid=0 | w=20
  1140. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> Xeroderma pigmentosum
    n1=en:peutz-jeghers syndrome | n2=Xeroderma pigmentosum | rel=r_associated | relid=0 | w=20
  1141. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> xeroderma pigmentosum
    n1=en:peutz-jeghers syndrome | n2=xeroderma pigmentosum | rel=r_associated | relid=0 | w=20
  1142. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> xérodermite pigmentaire
    n1=en:peutz-jeghers syndrome | n2=xérodermite pigmentaire | rel=r_associated | relid=0 | w=20
  1143. en:peutz-jeghers syndrome -- r_associated #0: 20 / 0.385 -> yellow nail syndrome
    n1=en:peutz-jeghers syndrome | n2=yellow nail syndrome | rel=r_associated | relid=0 | w=20
  1144. en:peutz-jeghers syndrome -- r_associated #0: 10 / 0.192 -> carcinologie
    (oncologie)
    n1=en:peutz-jeghers syndrome | n2=carcinologie
    (oncologie)
    | rel=r_associated | relid=0 | w=10
  1145. en:peutz-jeghers syndrome -- r_associated #0: 10 / 0.192 -> en:dermatology
    n1=en:peutz-jeghers syndrome | n2=en:dermatology | rel=r_associated | relid=0 | w=10
  1146. en:peutz-jeghers syndrome -- r_associated #0: 10 / 0.192 -> en:oncology
    n1=en:peutz-jeghers syndrome | n2=en:oncology | rel=r_associated | relid=0 | w=10
  1147. en:peutz-jeghers syndrome -- r_associated #0: 10 / 0.192 -> en:specialized branches of medicine
    n1=en:peutz-jeghers syndrome | n2=en:specialized branches of medicine | rel=r_associated | relid=0 | w=10
  1148. en:peutz-jeghers syndrome -- r_associated #0: 10 / 0.192 -> Spécialités médicales
    n1=en:peutz-jeghers syndrome | n2=Spécialités médicales | rel=r_associated | relid=0 | w=10
  1149. en:peutz-jeghers syndrome -- r_associated #0: 1 / 0.019 -> en:disease or syndrome
    n1=en:peutz-jeghers syndrome | n2=en:disease or syndrome | rel=r_associated | relid=0 | w=1
≈ 1390 relations entrantes

  1. atrophie du foie --- r_associated #0: 448 --> en:peutz-jeghers syndrome
    n1=atrophie du foie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=448
  2. atrophie hépatique --- r_associated #0: 447 --> en:peutz-jeghers syndrome
    n1=atrophie hépatique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=447
  3. en:atrophy of liver --- r_associated #0: 446 --> en:peutz-jeghers syndrome
    n1=en:atrophy of liver | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=446
  4. anomalie congénitale --- r_associated #0: 424 --> en:peutz-jeghers syndrome
    n1=anomalie congénitale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=424
  5. en:congenital abnormality --- r_associated #0: 421 --> en:peutz-jeghers syndrome
    n1=en:congenital abnormality | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=421
  6. malformation congénitale --- r_associated #0: 356 --> en:peutz-jeghers syndrome
    n1=malformation congénitale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=356
  7. en:congenital anomaly --- r_associated #0: 355 --> en:peutz-jeghers syndrome
    n1=en:congenital anomaly | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=355
  8. carcinome du pancreas --- r_associated #0: 328 --> en:peutz-jeghers syndrome
    n1=carcinome du pancreas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=328
  9. carcinome pancréatique --- r_associated #0: 322 --> en:peutz-jeghers syndrome
    n1=carcinome pancréatique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=322
  10. cancer pancréatique --- r_associated #0: 315 --> en:peutz-jeghers syndrome
    n1=cancer pancréatique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=315
  11. en:pancreatic carcinoma --- r_associated #0: 315 --> en:peutz-jeghers syndrome
    n1=en:pancreatic carcinoma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=315
  12. partie non précisée tumeur maligne du pancréas --- r_associated #0: 315 --> en:peutz-jeghers syndrome
    n1=partie non précisée tumeur maligne du pancréas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=315
  13. tumeur maligne pancréatique --- r_associated #0: 315 --> en:peutz-jeghers syndrome
    n1=tumeur maligne pancréatique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=315
  14. carcinome du pancréas --- r_associated #0: 314 --> en:peutz-jeghers syndrome
    n1=carcinome du pancréas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=314
  15. en:congenital defect --- r_associated #0: 310 --> en:peutz-jeghers syndrome
    n1=en:congenital defect | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=310
  16. tumeur pancréatique maligne --- r_associated #0: 305 --> en:peutz-jeghers syndrome
    n1=tumeur pancréatique maligne | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=305
  17. atrophie cutanée --- r_associated #0: 300 --> en:peutz-jeghers syndrome
    n1=atrophie cutanée | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=300
  18. déformation congénitale --- r_associated #0: 296 --> en:peutz-jeghers syndrome
    n1=déformation congénitale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=296
  19. déficience congénitale --- r_associated #0: 295 --> en:peutz-jeghers syndrome
    n1=déficience congénitale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=295
  20. tumeurs du pancreas --- r_associated #0: 295 --> en:peutz-jeghers syndrome
    n1=tumeurs du pancreas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=295
  21. en:skin atrophy --- r_associated #0: 291 --> en:peutz-jeghers syndrome
    n1=en:skin atrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=291
  22. atrophodermie --- r_associated #0: 285 --> en:peutz-jeghers syndrome
    n1=atrophodermie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=285
  23. en:marfan syndrome --- r_associated #0: 285 --> en:peutz-jeghers syndrome
    n1=en:marfan syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=285
  24. maladie de Marfan --- r_associated #0: 281 --> en:peutz-jeghers syndrome
    n1=maladie de Marfan | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=281
  25. syndrome de Marfan --- r_associated #0: 281 --> en:peutz-jeghers syndrome
    n1=syndrome de Marfan | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=281
  26. atrophie de la peau --- r_associated #0: 280 --> en:peutz-jeghers syndrome
    n1=atrophie de la peau | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=280
  27. tumeur maligne du pancréas --- r_associated #0: 280 --> en:peutz-jeghers syndrome
    n1=tumeur maligne du pancréas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=280
  28. cancer du pancréas --- r_associated #0: 276 --> en:peutz-jeghers syndrome
    n1=cancer du pancréas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=276
  29. tumeurs pancréatiques --- r_associated #0: 272 --> en:peutz-jeghers syndrome
    n1=tumeurs pancréatiques | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=272
  30. tumeur du pancréas --- r_associated #0: 270 --> en:peutz-jeghers syndrome
    n1=tumeur du pancréas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=270
  31. arachnodactylie --- r_associated #0: 261 --> en:peutz-jeghers syndrome
    n1=arachnodactylie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=261
  32. tumeurs du pancréas --- r_associated #0: 255 --> en:peutz-jeghers syndrome
    n1=tumeurs du pancréas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=255
  33. en:digestive system neoplasm --- r_associated #0: 251 --> en:peutz-jeghers syndrome
    n1=en:digestive system neoplasm | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=251
  34. néoplasie gastro-intestinale --- r_associated #0: 250 --> en:peutz-jeghers syndrome
    n1=néoplasie gastro-intestinale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=250
  35. tumeur gastro-intestinale --- r_associated #0: 250 --> en:peutz-jeghers syndrome
    n1=tumeur gastro-intestinale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=250
  36. tumeur gastrointestinale --- r_associated #0: 250 --> en:peutz-jeghers syndrome
    n1=tumeur gastrointestinale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=250
  37. atrophie --- r_associated #0: 237 --> en:peutz-jeghers syndrome
    n1=atrophie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=237
  38. en:atrophy --- r_associated #0: 235 --> en:peutz-jeghers syndrome
    n1=en:atrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=235
  39. en:arachnodactyly --- r_associated #0: 231 --> en:peutz-jeghers syndrome
    n1=en:arachnodactyly | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=231
  40. syndrome de soto --- r_associated #0: 210 --> en:peutz-jeghers syndrome
    n1=syndrome de soto | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=210
  41. kyste rétentionnel de l'ovaire --- r_associated #0: 205 --> en:peutz-jeghers syndrome
    n1=kyste rétentionnel de l'ovaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=205
  42. en:enzymology --- r_associated #0: 204 --> en:peutz-jeghers syndrome
    n1=en:enzymology | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=204
  43. en:ovarian cyst --- r_associated #0: 203 --> en:peutz-jeghers syndrome
    n1=en:ovarian cyst | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=203
  44. en:sotos syndrome --- r_associated #0: 202 --> en:peutz-jeghers syndrome
    n1=en:sotos syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=202
  45. gigantisme cérébral --- r_associated #0: 201 --> en:peutz-jeghers syndrome
    n1=gigantisme cérébral | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=201
  46. kyste ovarien --- r_associated #0: 201 --> en:peutz-jeghers syndrome
    n1=kyste ovarien | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=201
  47. kyste à l'ovaire --- r_associated #0: 201 --> en:peutz-jeghers syndrome
    n1=kyste à l'ovaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=201
  48. difformité congénitale --- r_associated #0: 200 --> en:peutz-jeghers syndrome
    n1=difformité congénitale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=200
  49. enzymologie --- r_associated #0: 200 --> en:peutz-jeghers syndrome
    n1=enzymologie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=200
  50. kyste de l'ovaire --- r_associated #0: 200 --> en:peutz-jeghers syndrome
    n1=kyste de l'ovaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=200
  51. kyste ovarien bénin --- r_associated #0: 200 --> en:peutz-jeghers syndrome
    n1=kyste ovarien bénin | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=200
  52. syndrome de Sotos --- r_associated #0: 195 --> en:peutz-jeghers syndrome
    n1=syndrome de Sotos | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=195
  53. en:sotos' syndrome --- r_associated #0: 190 --> en:peutz-jeghers syndrome
    n1=en:sotos' syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=190
  54. maladie congénitale --- r_associated #0: 190 --> en:peutz-jeghers syndrome
    n1=maladie congénitale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=190
  55. en:malignant pancreatic neoplasm --- r_associated #0: 185 --> en:peutz-jeghers syndrome
    n1=en:malignant pancreatic neoplasm | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=185
  56. en:osteomalacia --- r_associated #0: 185 --> en:peutz-jeghers syndrome
    n1=en:osteomalacia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=185
  57. pathologie congénitale --- r_associated #0: 185 --> en:peutz-jeghers syndrome
    n1=pathologie congénitale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=185
  58. polypose rhino-sinusienne déformante --- r_associated #0: 185 --> en:peutz-jeghers syndrome
    n1=polypose rhino-sinusienne déformante | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=185
  59. ostéomalacie --- r_associated #0: 184 --> en:peutz-jeghers syndrome
    n1=ostéomalacie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=184
  60. en:xeroderma pigmentosum --- r_associated #0: 183 --> en:peutz-jeghers syndrome
    n1=en:xeroderma pigmentosum | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=183
  61. en:polypoid sinus degeneration --- r_associated #0: 182 --> en:peutz-jeghers syndrome
    n1=en:polypoid sinus degeneration | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=182
  62. en:pancreatic neoplasm --- r_associated #0: 180 --> en:peutz-jeghers syndrome
    n1=en:pancreatic neoplasm | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=180
  63. en:walker-warburg syndrome --- r_associated #0: 180 --> en:peutz-jeghers syndrome
    n1=en:walker-warburg syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=180
  64. xeroderma pigmentosum --- r_associated #0: 179 --> en:peutz-jeghers syndrome
    n1=xeroderma pigmentosum | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=179
  65. syndrome de Walker-Warburg --- r_associated #0: 178 --> en:peutz-jeghers syndrome
    n1=syndrome de Walker-Warburg | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=178
  66. syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire --- r_associated #0: 169 --> en:peutz-jeghers syndrome
    n1=syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=169
  67. en:hereditary breast and ovarian cancer syndrome --- r_associated #0: 168 --> en:peutz-jeghers syndrome
    n1=en:hereditary breast and ovarian cancer syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=168
  68. en:parasitology --- r_associated #0: 164 --> en:peutz-jeghers syndrome
    n1=en:parasitology | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=164
  69. syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire --- r_associated #0: 164 --> en:peutz-jeghers syndrome
    n1=syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=164
  70. enzymology --- r_associated #0: 160 --> en:peutz-jeghers syndrome
    n1=enzymology | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=160
  71. parasitologie --- r_associated #0: 160 --> en:peutz-jeghers syndrome
    n1=parasitologie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=160
  72. dégénérescence polypoïde du sinus --- r_associated #0: 158 --> en:peutz-jeghers syndrome
    n1=dégénérescence polypoïde du sinus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=158
  73. syndrome héréditaire de cancer du sein et de l'ovaire --- r_associated #0: 158 --> en:peutz-jeghers syndrome
    n1=syndrome héréditaire de cancer du sein et de l'ovaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=158
  74. dégénérescence d'un polype sinusien --- r_associated #0: 157 --> en:peutz-jeghers syndrome
    n1=dégénérescence d'un polype sinusien | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=157
  75. atrophie optique autosomique dominante --- r_associated #0: 149 --> en:peutz-jeghers syndrome
    n1=atrophie optique autosomique dominante | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=149
  76. neuropathie héréditaire sensitive et autonome de type 1 --- r_associated #0: 148 --> en:peutz-jeghers syndrome
    n1=neuropathie héréditaire sensitive et autonome de type 1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=148
  77. syndrome d'Alagille --- r_associated #0: 147 --> en:peutz-jeghers syndrome
    n1=syndrome d'Alagille | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=147
  78. neuropathie héréditaire sensitive et autonome de type i --- r_associated #0: 145 --> en:peutz-jeghers syndrome
    n1=neuropathie héréditaire sensitive et autonome de type i | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=145
  79. neuropathie sensitive héréditaire dominante de type i --- r_associated #0: 145 --> en:peutz-jeghers syndrome
    n1=neuropathie sensitive héréditaire dominante de type i | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=145
  80. en:hereditary sensory autonomic neuropathy, type 1 --- r_associated #0: 141 --> en:peutz-jeghers syndrome
    n1=en:hereditary sensory autonomic neuropathy, type 1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=141
  81. anus praeter --- r_associated #0: 135 --> en:peutz-jeghers syndrome
    n1=anus praeter | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=135
  82. chondrodysplasie héréditaire déformante --- r_associated #0: 135 --> en:peutz-jeghers syndrome
    n1=chondrodysplasie héréditaire déformante | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=135
  83. en:preternatural anus --- r_associated #0: 133 --> en:peutz-jeghers syndrome
    n1=en:preternatural anus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=133
  84. anus contre nature --- r_associated #0: 131 --> en:peutz-jeghers syndrome
    n1=anus contre nature | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=131
  85. aclasie diaphysaire --- r_associated #0: 130 --> en:peutz-jeghers syndrome
    n1=aclasie diaphysaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=130
  86. en:congenital malformation --- r_associated #0: 130 --> en:peutz-jeghers syndrome
    n1=en:congenital malformation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=130
  87. exostose héréditaire multiple --- r_associated #0: 130 --> en:peutz-jeghers syndrome
    n1=exostose héréditaire multiple | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=130
  88. en:hereditary multiple exostoses --- r_associated #0: 129 --> en:peutz-jeghers syndrome
    n1=en:hereditary multiple exostoses | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=129
  89. maladie exostosante multiple --- r_associated #0: 125 --> en:peutz-jeghers syndrome
    n1=maladie exostosante multiple | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=125
  90. chondrodysplasie déformante héréditaire --- r_associated #0: 120 --> en:peutz-jeghers syndrome
    n1=chondrodysplasie déformante héréditaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=120
  91. en:birth defect --- r_associated #0: 120 --> en:peutz-jeghers syndrome
    n1=en:birth defect | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=120
  92. maladie ostéogénique --- r_associated #0: 115 --> en:peutz-jeghers syndrome
    n1=maladie ostéogénique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=115
  93. prolapsus de la muqueuse rectale --- r_associated #0: 115 --> en:peutz-jeghers syndrome
    n1=prolapsus de la muqueuse rectale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=115
  94. Warburg --- r_associated #0: 114 --> en:peutz-jeghers syndrome
    n1=Warburg | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=114
  95. en:yellow nail syndrome --- r_associated #0: 110 --> en:peutz-jeghers syndrome
    n1=en:yellow nail syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=110
  96. maladie de Bessel-Hagen --- r_associated #0: 110 --> en:peutz-jeghers syndrome
    n1=maladie de Bessel-Hagen | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=110
  97. prolapsus du rectum --- r_associated #0: 110 --> en:peutz-jeghers syndrome
    n1=prolapsus du rectum | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=110
  98. en:piebaldism --- r_associated #0: 108 --> en:peutz-jeghers syndrome
    n1=en:piebaldism | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=108
  99. yellow nail syndrome --- r_associated #0: 108 --> en:peutz-jeghers syndrome
    n1=yellow nail syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=108
  100. en:rectal prolapse --- r_associated #0: 107 --> en:peutz-jeghers syndrome
    n1=en:rectal prolapse | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=107
  101. ostéodystrophie --- r_associated #0: 107 --> en:peutz-jeghers syndrome
    n1=ostéodystrophie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=107
  102. affections atrophiques de la peau --- r_associated #0: 105 --> en:peutz-jeghers syndrome
    n1=affections atrophiques de la peau | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=105
  103. maladie des exostoses multiples --- r_associated #0: 105 --> en:peutz-jeghers syndrome
    n1=maladie des exostoses multiples | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=105
  104. neuropathie sensitive héréditaire dominante de type I --- r_associated #0: 105 --> en:peutz-jeghers syndrome
    n1=neuropathie sensitive héréditaire dominante de type I | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=105
  105. piebaldisme --- r_associated #0: 105 --> en:peutz-jeghers syndrome
    n1=piebaldisme | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=105
  106. prolapsus rectal --- r_associated #0: 105 --> en:peutz-jeghers syndrome
    n1=prolapsus rectal | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=105
  107. tumeur bénigne pancréatique --- r_associated #0: 105 --> en:peutz-jeghers syndrome
    n1=tumeur bénigne pancréatique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=105
  108. en:osteodystrophy --- r_associated #0: 104 --> en:peutz-jeghers syndrome
    n1=en:osteodystrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=104
  109. piébaldisme --- r_associated #0: 104 --> en:peutz-jeghers syndrome
    n1=piébaldisme | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=104
  110. mélasma --- r_associated #0: 102 --> en:peutz-jeghers syndrome
    n1=mélasma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=102
  111. dystrophy --- r_associated #0: 100 --> en:peutz-jeghers syndrome
    n1=dystrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=100
  112. en:melasma --- r_associated #0: 100 --> en:peutz-jeghers syndrome
    n1=en:melasma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=100
  113. onychodystrophie --- r_associated #0: 100 --> en:peutz-jeghers syndrome
    n1=onychodystrophie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=100
  114. chérubisme --- r_associated #0: 99 --> en:peutz-jeghers syndrome
    n1=chérubisme | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=99
  115. en:onychodystrophy --- r_associated #0: 99 --> en:peutz-jeghers syndrome
    n1=en:onychodystrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=99
  116. en:benign pancreatic neoplasm --- r_associated #0: 97 --> en:peutz-jeghers syndrome
    n1=en:benign pancreatic neoplasm | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=97
  117. tumeur bénigne du pancréas --- r_associated #0: 97 --> en:peutz-jeghers syndrome
    n1=tumeur bénigne du pancréas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=97
  118. atrésie de l'oesophage --- r_associated #0: 96 --> en:peutz-jeghers syndrome
    n1=atrésie de l'oesophage | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=96
  119. atrésie de l'œsophage --- r_associated #0: 96 --> en:peutz-jeghers syndrome
    n1=atrésie de l'œsophage | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=96
  120. en:steatohepatitis --- r_associated #0: 96 --> en:peutz-jeghers syndrome
    n1=en:steatohepatitis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=96
  121. atrésie de l'œsophage --- r_associated #0: 95 --> en:peutz-jeghers syndrome
    n1=atrésie de l'œsophage | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=95
  122. en:cherubism --- r_associated #0: 95 --> en:peutz-jeghers syndrome
    n1=en:cherubism | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=95
  123. stéatohépatite --- r_associated #0: 95 --> en:peutz-jeghers syndrome
    n1=stéatohépatite | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=95
  124. en:dystrophy --- r_associated #0: 92 --> en:peutz-jeghers syndrome
    n1=en:dystrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=92
  125. en:benign tumor of pancreas --- r_associated #0: 91 --> en:peutz-jeghers syndrome
    n1=en:benign tumor of pancreas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=91
  126. malformations de la bouche --- r_associated #0: 91 --> en:peutz-jeghers syndrome
    n1=malformations de la bouche | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=91
  127. en:pancreatic cancer --- r_associated #0: 90 --> en:peutz-jeghers syndrome
    n1=en:pancreatic cancer | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=90
  128. poumon vert --- r_associated #0: 90 --> en:peutz-jeghers syndrome
    n1=poumon vert | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=90
  129. protéinose alvéolaire --- r_associated #0: 90 --> en:peutz-jeghers syndrome
    n1=protéinose alvéolaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=90
  130. protéinose alvéolaire pulmonaire --- r_associated #0: 90 --> en:peutz-jeghers syndrome
    n1=protéinose alvéolaire pulmonaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=90
  131. en:lung --- r_associated #0: 89 --> en:peutz-jeghers syndrome
    n1=en:lung | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=89
  132. en:pulmonary alveolar proteinosis --- r_associated #0: 87 --> en:peutz-jeghers syndrome
    n1=en:pulmonary alveolar proteinosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=87
  133. lung --- r_associated #0: 85 --> en:peutz-jeghers syndrome
    n1=lung | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=85
  134. tare congénitale --- r_associated #0: 85 --> en:peutz-jeghers syndrome
    n1=tare congénitale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=85
  135. anomalies buccales --- r_associated #0: 84 --> en:peutz-jeghers syndrome
    n1=anomalies buccales | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=84
  136. en:mouth abnormalities --- r_associated #0: 83 --> en:peutz-jeghers syndrome
    n1=en:mouth abnormalities | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=83
  137. artério-sclérose --- r_associated #0: 82 --> en:peutz-jeghers syndrome
    n1=artério-sclérose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=82
  138. artériosclérose --- r_associated #0: 80 --> en:peutz-jeghers syndrome
    n1=artériosclérose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=80
  139. en:exania --- r_associated #0: 80 --> en:peutz-jeghers syndrome
    n1=en:exania | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=80
  140. anomalies de la bouche --- r_associated #0: 77 --> en:peutz-jeghers syndrome
    n1=anomalies de la bouche | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=77
  141. congenital --- r_associated #0: 76 --> en:peutz-jeghers syndrome
    n1=congenital | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=76
  142. distrophie --- r_associated #0: 75 --> en:peutz-jeghers syndrome
    n1=distrophie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=75
  143. en:multiple osteogenic exostoses --- r_associated #0: 75 --> en:peutz-jeghers syndrome
    n1=en:multiple osteogenic exostoses | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=75
  144. albinisme --- r_associated #0: 74 --> en:peutz-jeghers syndrome
    n1=albinisme | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=74
  145. en:congenital --- r_associated #0: 74 --> en:peutz-jeghers syndrome
    n1=en:congenital | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=74
  146. tophus --- r_associated #0: 74 --> en:peutz-jeghers syndrome
    n1=tophus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=74
  147. en:albinism --- r_associated #0: 72 --> en:peutz-jeghers syndrome
    n1=en:albinism | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=72
  148. en:tophus --- r_associated #0: 72 --> en:peutz-jeghers syndrome
    n1=en:tophus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=72
  149. en:Sotos' syndrome --- r_associated #0: 70 --> en:peutz-jeghers syndrome
    n1=en:Sotos' syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=70
  150. en:arteriosclerosis --- r_associated #0: 67 --> en:peutz-jeghers syndrome
    n1=en:arteriosclerosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=67
  151. hyperbilirubinémie --- r_associated #0: 67 --> en:peutz-jeghers syndrome
    n1=hyperbilirubinémie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=67
  152. bilirubinémie --- r_associated #0: 65 --> en:peutz-jeghers syndrome
    n1=bilirubinémie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=65
  153. congénitale --- r_associated #0: 65 --> en:peutz-jeghers syndrome
    n1=congénitale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=65
  154. en:dubin-johnson syndrome --- r_associated #0: 64 --> en:peutz-jeghers syndrome
    n1=en:dubin-johnson syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=64
  155. albinoïdisme --- r_associated #0: 63 --> en:peutz-jeghers syndrome
    n1=albinoïdisme | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=63
  156. malformations buccales --- r_associated #0: 62 --> en:peutz-jeghers syndrome
    n1=malformations buccales | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=62
  157. syndrome de Gorlin --- r_associated #0: 61 --> en:peutz-jeghers syndrome
    n1=syndrome de Gorlin | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=61
  158. Cancer colorectal héréditaire sans polypose --- r_associated #0: 60 --> en:peutz-jeghers syndrome
    n1=Cancer colorectal héréditaire sans polypose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=60
  159. Went (atrophie optique liée au sexe de) --- r_associated #0: 60 --> en:peutz-jeghers syndrome
    n1=Went (atrophie optique liée au sexe de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=60
  160. en:pretematural anus --- r_associated #0: 60 --> en:peutz-jeghers syndrome
    n1=en:pretematural anus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=60
  161. naevomatose baso-cellulaire --- r_associated #0: 60 --> en:peutz-jeghers syndrome
    n1=naevomatose baso-cellulaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=60
  162. syndrome de dubin-johnson --- r_associated #0: 60 --> en:peutz-jeghers syndrome
    n1=syndrome de dubin-johnson | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=60
  163. en:albinoidism --- r_associated #0: 59 --> en:peutz-jeghers syndrome
    n1=en:albinoidism | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=59
  164. naevomatose basocellulaire --- r_associated #0: 59 --> en:peutz-jeghers syndrome
    n1=naevomatose basocellulaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=59
  165. congénital --- r_associated #0: 58 --> en:peutz-jeghers syndrome
    n1=congénital | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=58
  166. en:demyelination --- r_associated #0: 58 --> en:peutz-jeghers syndrome
    n1=en:demyelination | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=58
  167. démyélinisation --- r_associated #0: 56 --> en:peutz-jeghers syndrome
    n1=démyélinisation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=56
  168. en:optic atrophy --- r_associated #0: 56 --> en:peutz-jeghers syndrome
    n1=en:optic atrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=56
  169. maladie neurodégénérative du système nerveux central --- r_associated #0: 56 --> en:peutz-jeghers syndrome
    n1=maladie neurodégénérative du système nerveux central | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=56
  170. neurofibromatose de type 1 --- r_associated #0: 56 --> en:peutz-jeghers syndrome
    n1=neurofibromatose de type 1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=56
  171. syndrome de Dubin-Johnson --- r_associated #0: 56 --> en:peutz-jeghers syndrome
    n1=syndrome de Dubin-Johnson | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=56
  172. Völker-Dieben (atrophie optique liée au sexe de) --- r_associated #0: 55 --> en:peutz-jeghers syndrome
    n1=Völker-Dieben (atrophie optique liée au sexe de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=55
  173. Xeroderma pigmentosum --- r_associated #0: 55 --> en:peutz-jeghers syndrome
    n1=Xeroderma pigmentosum | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=55
  174. cancer colorectal héréditaire sans polypose --- r_associated #0: 55 --> en:peutz-jeghers syndrome
    n1=cancer colorectal héréditaire sans polypose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=55
  175. vestige du conduit vitellin --- r_associated #0: 55 --> en:peutz-jeghers syndrome
    n1=vestige du conduit vitellin | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=55
  176. dysplasie cléidocrânienne --- r_associated #0: 54 --> en:peutz-jeghers syndrome
    n1=dysplasie cléidocrânienne | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=54
  177. en:central nervous system degenerative disorder --- r_associated #0: 54 --> en:peutz-jeghers syndrome
    n1=en:central nervous system degenerative disorder | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=54
  178. en:hyperbilirubinemia --- r_associated #0: 54 --> en:peutz-jeghers syndrome
    n1=en:hyperbilirubinemia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=54
  179. vice de conformation --- r_associated #0: 54 --> en:peutz-jeghers syndrome
    n1=vice de conformation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=54
  180. en:nystagmus --- r_associated #0: 52 --> en:peutz-jeghers syndrome
    n1=en:nystagmus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=52
  181. cancer colo-rectal héréditaire sans polypose --- r_associated #0: 51 --> en:peutz-jeghers syndrome
    n1=cancer colo-rectal héréditaire sans polypose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=51
  182. en:byssinosis --- r_associated #0: 51 --> en:peutz-jeghers syndrome
    n1=en:byssinosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=51
  183. en:mccune-albright syndrome --- r_associated #0: 51 --> en:peutz-jeghers syndrome
    n1=en:mccune-albright syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=51
  184. en:meckel diverticulum --- r_associated #0: 51 --> en:peutz-jeghers syndrome
    n1=en:meckel diverticulum | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=51
  185. maladie clinique de recklinghausen --- r_associated #0: 51 --> en:peutz-jeghers syndrome
    n1=maladie clinique de recklinghausen | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=51
  186. Épidermolyse bulleuse acquise --- r_associated #0: 51 --> en:peutz-jeghers syndrome
    n1=Épidermolyse bulleuse acquise | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=51
  187. épidermolyse bulleuse acquise --- r_associated #0: 51 --> en:peutz-jeghers syndrome
    n1=épidermolyse bulleuse acquise | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=51
  188. atrophie optique liée au sexe --- r_associated #0: 50 --> en:peutz-jeghers syndrome
    n1=atrophie optique liée au sexe | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=50
  189. dysplasie cléido-crânienne --- r_associated #0: 50 --> en:peutz-jeghers syndrome
    n1=dysplasie cléido-crânienne | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=50
  190. en:Miller's disease --- r_associated #0: 50 --> en:peutz-jeghers syndrome
    n1=en:Miller's disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=50
  191. en:feebleness --- r_associated #0: 50 --> en:peutz-jeghers syndrome
    n1=en:feebleness | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=50
  192. en:teratosis --- r_associated #0: 50 --> en:peutz-jeghers syndrome
    n1=en:teratosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=50
  193. nystagmus --- r_associated #0: 50 --> en:peutz-jeghers syndrome
    n1=nystagmus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=50
  194. polypose colique familiale --- r_associated #0: 50 --> en:peutz-jeghers syndrome
    n1=polypose colique familiale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=50
  195. xanthomatose cérébrotendineuse de Van Bogaert --- r_associated #0: 50 --> en:peutz-jeghers syndrome
    n1=xanthomatose cérébrotendineuse de Van Bogaert | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=50
  196. xérodermite pigmentaire --- r_associated #0: 50 --> en:peutz-jeghers syndrome
    n1=xérodermite pigmentaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=50
  197. Recklinghausen (neurofibromatose de) --- r_associated #0: 49 --> en:peutz-jeghers syndrome
    n1=Recklinghausen (neurofibromatose de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=49
  198. atrophie optique liée au sexe de Völker-Dieben --- r_associated #0: 49 --> en:peutz-jeghers syndrome
    n1=atrophie optique liée au sexe de Völker-Dieben | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=49
  199. en:X-linked --- r_associated #0: 49 --> en:peutz-jeghers syndrome
    n1=en:X-linked | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=49
  200. en:congenital ichthyosis --- r_associated #0: 49 --> en:peutz-jeghers syndrome
    n1=en:congenital ichthyosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=49
  201. en:familial adenomatous polyposis --- r_associated #0: 49 --> en:peutz-jeghers syndrome
    n1=en:familial adenomatous polyposis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=49
  202. anomalie du développement --- r_associated #0: 48 --> en:peutz-jeghers syndrome
    n1=anomalie du développement | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=48
  203. en:Marfan's syndrome --- r_associated #0: 48 --> en:peutz-jeghers syndrome
    n1=en:Marfan's syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=48
  204. en:hereditary nonpolyposis colorectal cancer --- r_associated #0: 48 --> en:peutz-jeghers syndrome
    n1=en:hereditary nonpolyposis colorectal cancer | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=48
  205. ichthyose congénitale --- r_associated #0: 48 --> en:peutz-jeghers syndrome
    n1=ichthyose congénitale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=48
  206. byssinosis --- r_associated #0: 47 --> en:peutz-jeghers syndrome
    n1=byssinosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=47
  207. diverticule de Meckel --- r_associated #0: 47 --> en:peutz-jeghers syndrome
    n1=diverticule de Meckel | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=47
  208. en:epidermolysis bullosa acquisita --- r_associated #0: 47 --> en:peutz-jeghers syndrome
    n1=en:epidermolysis bullosa acquisita | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=47
  209. en:multifocal motor neuropathy --- r_associated #0: 47 --> en:peutz-jeghers syndrome
    n1=en:multifocal motor neuropathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=47
  210. polypose rectocolique --- r_associated #0: 47 --> en:peutz-jeghers syndrome
    n1=polypose rectocolique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=47
  211. en:cerebrotendinous xanthomatosis --- r_associated #0: 46 --> en:peutz-jeghers syndrome
    n1=en:cerebrotendinous xanthomatosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=46
  212. en:physical defect --- r_associated #0: 46 --> en:peutz-jeghers syndrome
    n1=en:physical defect | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=46
  213. maladie de Recklinghausen --- r_associated #0: 46 --> en:peutz-jeghers syndrome
    n1=maladie de Recklinghausen | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=46
  214. maladie de von Recklinghausen --- r_associated #0: 46 --> en:peutz-jeghers syndrome
    n1=maladie de von Recklinghausen | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=46
  215. syndrome de peutz-jeghers --- r_associated #0: 46 --> en:peutz-jeghers syndrome
    n1=syndrome de peutz-jeghers | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=46
  216. xanthomatose cérébro-tendineuse --- r_associated #0: 46 --> en:peutz-jeghers syndrome
    n1=xanthomatose cérébro-tendineuse | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=46
  217. xanthomatose cérébrotendineuse --- r_associated #0: 46 --> en:peutz-jeghers syndrome
    n1=xanthomatose cérébrotendineuse | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=46
  218. en:alveolar proteinosis --- r_associated #0: 45 --> en:peutz-jeghers syndrome
    n1=en:alveolar proteinosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=45
  219. en:neurofibromatosis --- r_associated #0: 45 --> en:peutz-jeghers syndrome
    n1=en:neurofibromatosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=45
  220. en:nevoid basal cell carcinoma syndrome --- r_associated #0: 45 --> en:peutz-jeghers syndrome
    n1=en:nevoid basal cell carcinoma syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=45
  221. en:von Recklinghausen's disease --- r_associated #0: 45 --> en:peutz-jeghers syndrome
    n1=en:von Recklinghausen's disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=45
  222. neuropathie motrice multifocale --- r_associated #0: 45 --> en:peutz-jeghers syndrome
    n1=neuropathie motrice multifocale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=45
  223. syndrome de McCune-Albright --- r_associated #0: 45 --> en:peutz-jeghers syndrome
    n1=syndrome de McCune-Albright | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=45
  224. syndrome de douleur extrême paroxystique --- r_associated #0: 45 --> en:peutz-jeghers syndrome
    n1=syndrome de douleur extrême paroxystique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=45
  225. syndrome oculo-cérébral avec hypopigmentation --- r_associated #0: 45 --> en:peutz-jeghers syndrome
    n1=syndrome oculo-cérébral avec hypopigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=45
  226. van Bogaert (xanthomatose cérébrotendineuse de) --- r_associated #0: 45 --> en:peutz-jeghers syndrome
    n1=van Bogaert (xanthomatose cérébrotendineuse de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=45
  227. Kjer (atrophie optique de type) --- r_associated #0: 44 --> en:peutz-jeghers syndrome
    n1=Kjer (atrophie optique de type) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=44
  228. en:neurofibromatosis type 1 --- r_associated #0: 44 --> en:peutz-jeghers syndrome
    n1=en:neurofibromatosis type 1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=44
  229. en:paroxysmal extreme pain disorder --- r_associated #0: 44 --> en:peutz-jeghers syndrome
    n1=en:paroxysmal extreme pain disorder | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=44
  230. neurofibromatose de Recklinghausen --- r_associated #0: 44 --> en:peutz-jeghers syndrome
    n1=neurofibromatose de Recklinghausen | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=44
  231. en:aniridia and intellectual disability syndrome --- r_associated #0: 43 --> en:peutz-jeghers syndrome
    n1=en:aniridia and intellectual disability syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=43
  232. en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome --- r_associated #0: 43 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=43
  233. en:bamforth syndrome --- r_associated #0: 43 --> en:peutz-jeghers syndrome
    n1=en:bamforth syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=43
  234. en:congenital intestinal obstruction --- r_associated #0: 43 --> en:peutz-jeghers syndrome
    n1=en:congenital intestinal obstruction | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=43
  235. en:ectodermal dysplasia/ skin fragility syndrome --- r_associated #0: 43 --> en:peutz-jeghers syndrome
    n1=en:ectodermal dysplasia/ skin fragility syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=43
  236. en:epidemiologic --- r_associated #0: 43 --> en:peutz-jeghers syndrome
    n1=en:epidemiologic | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=43
  237. en:syndactyly, type i --- r_associated #0: 43 --> en:peutz-jeghers syndrome
    n1=en:syndactyly, type i | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=43
  238. en:waardenburg syndrome type 4 --- r_associated #0: 43 --> en:peutz-jeghers syndrome
    n1=en:waardenburg syndrome type 4 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=43
  239. nystagmus lié au sexe --- r_associated #0: 43 --> en:peutz-jeghers syndrome
    n1=nystagmus lié au sexe | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=43
  240. Cancer du pancréas --- r_associated #0: 42 --> en:peutz-jeghers syndrome
    n1=Cancer du pancréas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=42
  241. Rendu-Osler (angiomatose hémorragique héréditaire ou familiale de) --- r_associated #0: 42 --> en:peutz-jeghers syndrome
    n1=Rendu-Osler (angiomatose hémorragique héréditaire ou familiale de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=42
  242. en:Marfan's disease --- r_associated #0: 42 --> en:peutz-jeghers syndrome
    n1=en:Marfan's disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=42
  243. en:aniridia, ptosis, intellectual disability, familial obesity syndrome --- r_associated #0: 42 --> en:peutz-jeghers syndrome
    n1=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=42
  244. en:brown-vialetto-van laere syndrome --- r_associated #0: 42 --> en:peutz-jeghers syndrome
    n1=en:brown-vialetto-van laere syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=42
  245. en:intestinal pseudo-obstruction --- r_associated #0: 42 --> en:peutz-jeghers syndrome
    n1=en:intestinal pseudo-obstruction | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=42
  246. en:lumbosacral spondylosis without myelopathy --- r_associated #0: 42 --> en:peutz-jeghers syndrome
    n1=en:lumbosacral spondylosis without myelopathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=42
  247. en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome --- r_associated #0: 42 --> en:peutz-jeghers syndrome
    n1=en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=42
  248. en:proteus-like syndrome (disorder) --- r_associated #0: 42 --> en:peutz-jeghers syndrome
    n1=en:proteus-like syndrome (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=42
  249. en:urticaria pigmentosa/maculopapular cutaneous mastocytosis --- r_associated #0: 42 --> en:peutz-jeghers syndrome
    n1=en:urticaria pigmentosa/maculopapular cutaneous mastocytosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=42
  250. syndrome de Peutz-Jeghers --- r_associated #0: 42 --> en:peutz-jeghers syndrome
    n1=syndrome de Peutz-Jeghers | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=42
  251. syndrome de marfan --- r_associated #0: 42 --> en:peutz-jeghers syndrome
    n1=syndrome de marfan | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=42
  252. en:acquired epidermolysis bullosa --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=en:acquired epidermolysis bullosa | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  253. en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  254. en:episodic ataxia --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=en:episodic ataxia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  255. en:esophageal atresia --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=en:esophageal atresia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  256. en:familial median cleft of upper and lower lip --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=en:familial median cleft of upper and lower lip | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  257. en:hereditary hemorrhagic telangiectasia --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=en:hereditary hemorrhagic telangiectasia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  258. en:hyperpigmented macules of lips --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=en:hyperpigmented macules of lips | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  259. en:major physical defect --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=en:major physical defect | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  260. en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  261. en:oculocerebral syndrome with hypopigmentation --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=en:oculocerebral syndrome with hypopigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  262. maladie de marfan --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=maladie de marfan | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  263. polypose adénomateuse familiale --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=polypose adénomateuse familiale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  264. polypose recto-colique familiale --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=polypose recto-colique familiale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  265. polypose rectocolique familiale --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=polypose rectocolique familiale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  266. retard mental, retard de croissance, surdité, microgénitalisme lié au sexe --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  267. rhabdomyolyse --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=rhabdomyolyse | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  268. syndrome de Treft-Sanborn-Carey --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=syndrome de Treft-Sanborn-Carey | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  269. syndrome de sotos --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=syndrome de sotos | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  270. télangiectasie hémorragique héréditaire --- r_associated #0: 41 --> en:peutz-jeghers syndrome
    n1=télangiectasie hémorragique héréditaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=41
  271. Walker-Warburg (syndrome de) --- r_associated #0: 40 --> en:peutz-jeghers syndrome
    n1=Walker-Warburg (syndrome de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=40
  272. dystonie dopasensible --- r_associated #0: 40 --> en:peutz-jeghers syndrome
    n1=dystonie dopasensible | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=40
  273. dystrophie --- r_associated #0: 40 --> en:peutz-jeghers syndrome
    n1=dystrophie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=40
  274. en:Peutz-Jeghers syndrome --- r_associated #0: 40 --> en:peutz-jeghers syndrome
    n1=en:Peutz-Jeghers syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=40
  275. en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia --- r_associated #0: 40 --> en:peutz-jeghers syndrome
    n1=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=40
  276. en:brachydactyly type a6 --- r_associated #0: 40 --> en:peutz-jeghers syndrome
    n1=en:brachydactyly type a6 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=40
  277. en:gaze palsy, familial horizontal, with progressive scoliosis --- r_associated #0: 40 --> en:peutz-jeghers syndrome
    n1=en:gaze palsy, familial horizontal, with progressive scoliosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=40
  278. en:type Völker-Dieben --- r_associated #0: 40 --> en:peutz-jeghers syndrome
    n1=en:type Völker-Dieben | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=40
  279. neurofibromatose de recklinghausen --- r_associated #0: 40 --> en:peutz-jeghers syndrome
    n1=neurofibromatose de recklinghausen | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=40
  280. pancréas (cancer du) --- r_associated #0: 40 --> en:peutz-jeghers syndrome
    n1=pancréas (cancer du) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=40
  281. sclérose artérielle --- r_associated #0: 40 --> en:peutz-jeghers syndrome
    n1=sclérose artérielle | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=40
  282. tophus goutteux --- r_associated #0: 40 --> en:peutz-jeghers syndrome
    n1=tophus goutteux | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=40
  283. en:Mohr-Tranebjaerg syndrome --- r_associated #0: 39 --> en:peutz-jeghers syndrome
    n1=en:Mohr-Tranebjaerg syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=39
  284. en:anorectal agenesis --- r_associated #0: 39 --> en:peutz-jeghers syndrome
    n1=en:anorectal agenesis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=39
  285. en:beckwith-wiedemann syndrome --- r_associated #0: 39 --> en:peutz-jeghers syndrome
    n1=en:beckwith-wiedemann syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=39
  286. en:disorder of central nervous system due to xeroderma pigmentosum --- r_associated #0: 39 --> en:peutz-jeghers syndrome
    n1=en:disorder of central nervous system due to xeroderma pigmentosum | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=39
  287. en:dopa-responsive dystonia --- r_associated #0: 39 --> en:peutz-jeghers syndrome
    n1=en:dopa-responsive dystonia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=39
  288. en:periventricular heterotopia, x-linked --- r_associated #0: 39 --> en:peutz-jeghers syndrome
    n1=en:periventricular heterotopia, x-linked | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=39
  289. lipofuscinose neuronale céroïde --- r_associated #0: 39 --> en:peutz-jeghers syndrome
    n1=lipofuscinose neuronale céroïde | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=39
  290. neurofibromatose de type périphérique --- r_associated #0: 39 --> en:peutz-jeghers syndrome
    n1=neurofibromatose de type périphérique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=39
  291. nystagmus congénital isolé --- r_associated #0: 39 --> en:peutz-jeghers syndrome
    n1=nystagmus congénital isolé | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=39
  292. Prolapsus rectal --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=Prolapsus rectal | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  293. en:Nijmegen breakage syndrome --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=en:Nijmegen breakage syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  294. en:Peutz-Jeghers' syndrome --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=en:Peutz-Jeghers' syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  295. en:aphalangy and syndactyly with microcephaly syndrome --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=en:aphalangy and syndactyly with microcephaly syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  296. en:familial non-autoimmune autosomal dominant hyperthyroidism --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=en:familial non-autoimmune autosomal dominant hyperthyroidism | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  297. en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  298. en:macies --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=en:macies | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  299. en:melanosis of vulva --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=en:melanosis of vulva | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  300. en:perniola krajewska carnevale syndrome --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=en:perniola krajewska carnevale syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  301. en:preaxial deficiency, postaxial polydactyly and hypospadias --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=en:preaxial deficiency, postaxial polydactyly and hypospadias | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  302. en:schwannomatosis --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=en:schwannomatosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  303. en:therapeutic aspects --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=en:therapeutic aspects | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  304. onycho-patellaire (syndrome) --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=onycho-patellaire (syndrome) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  305. poumon --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=poumon | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  306. sclérose des artères --- r_associated #0: 38 --> en:peutz-jeghers syndrome
    n1=sclérose des artères | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=38
  307. dystrophie des cônes liée au sexe --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=dystrophie des cônes liée au sexe | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  308. en:McCune-Albright's syndrome --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=en:McCune-Albright's syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  309. en:Pitt-Hopkins syndrome --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=en:Pitt-Hopkins syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  310. en:autosomal dominant excess of transthyretin --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant excess of transthyretin | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  311. en:chondromalacia of left knee --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=en:chondromalacia of left knee | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  312. en:chronic berylliosis --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=en:chronic berylliosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  313. en:cowden syndrome --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=en:cowden syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  314. en:hyperinsulinemic hypoglycemia, familial, 6 --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=en:hyperinsulinemic hypoglycemia, familial, 6 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  315. en:neurocutaneous melanosis sequence --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=en:neurocutaneous melanosis sequence | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  316. en:neuronal ceroid lipofuscinosis --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=en:neuronal ceroid lipofuscinosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  317. en:phakomatosis --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=en:phakomatosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  318. en:rhabdomyolysis --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=en:rhabdomyolysis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  319. exostosante (maladie) --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=exostosante (maladie) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  320. neuropathie tropicale ataxique --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=neuropathie tropicale ataxique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  321. paraplégie spastique avec atrophie optique et démence --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=paraplégie spastique avec atrophie optique et démence | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  322. poïkilodermatomyosite de Petges et Cléjat --- r_associated #0: 37 --> en:peutz-jeghers syndrome
    n1=poïkilodermatomyosite de Petges et Cléjat | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=37
  323. dystrophie des cônes liée au sexe avec reflet rétinien jaune-vert --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=dystrophie des cônes liée au sexe avec reflet rétinien jaune-vert | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  324. en:Lynch'syndrome --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:Lynch'syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  325. en:basal cell nevus syndrome --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:basal cell nevus syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  326. en:capillary malformation-arteriovenous malformation (disorder) --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:capillary malformation-arteriovenous malformation (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  327. en:cerebral gigantism --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:cerebral gigantism | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  328. en:kidney wilms tumor --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:kidney wilms tumor | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  329. en:laurin-sandrow syndrome --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:laurin-sandrow syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  330. en:lissencephaly syndrome, norman-roberts type --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:lissencephaly syndrome, norman-roberts type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  331. en:megalencephalic leukoencephalopathy with subcortical cysts --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:megalencephalic leukoencephalopathy with subcortical cysts | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  332. en:nijmegen breakage syndrome --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:nijmegen breakage syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  333. en:papillary muscle atrophy --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:papillary muscle atrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  334. en:pitt-hopkins syndrome --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:pitt-hopkins syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  335. en:poikilodermatomyositis --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:poikilodermatomyositis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  336. en:spondyloperipheral dysplasia short ulna --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:spondyloperipheral dysplasia short ulna | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  337. en:tropical ataxic neuropathy --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:tropical ataxic neuropathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  338. en:wyburn mason's syndrome --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:wyburn mason's syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  339. en:x-linked intellectual disability with acromegaly and hyperactivity syndrome --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  340. imperforation anale --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=imperforation anale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  341. néoplasie endocrinienne multiple (MEN 2B ou 3) --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=néoplasie endocrinienne multiple (MEN 2B ou 3) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  342. oculo-cérébral avec hypopigmentation (syndrome) --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=oculo-cérébral avec hypopigmentation (syndrome) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  343. stomatocytose héréditaire --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=stomatocytose héréditaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  344. syndrome de Lynch --- r_associated #0: 36 --> en:peutz-jeghers syndrome
    n1=syndrome de Lynch | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=36
  345. Diverticule de Meckel --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=Diverticule de Meckel | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  346. acrodermatite entéropathique --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=acrodermatite entéropathique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  347. déminéralisation osseuse --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=déminéralisation osseuse | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  348. en:Lynch syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:Lynch syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  349. en:abdominal wall cyst --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:abdominal wall cyst | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  350. en:acrodermatitis enteropathica --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:acrodermatitis enteropathica | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  351. en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  352. en:alpha-methylacyl-coa racemase deficiency --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:alpha-methylacyl-coa racemase deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  353. en:atrophic thrush --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:atrophic thrush | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  354. en:atrophoderma vermiculatum --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:atrophoderma vermiculatum | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  355. en:autosomal dominant charcot-marie-tooth disease type 2m --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant charcot-marie-tooth disease type 2m | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  356. en:autosomal dominant ichthyosis vulgaris --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant ichthyosis vulgaris | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  357. en:autosomal dominant inheritance --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant inheritance | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  358. en:autosomal dominant muscular dystrophy not predominantly limb girdle --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant muscular dystrophy not predominantly limb girdle | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  359. en:autosomal dominant oculocutaneous albinism --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant oculocutaneous albinism | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  360. en:autosomal dominant palmoplantar keratoderma and congenital alopecia --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  361. en:blepharal pigmentation --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:blepharal pigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  362. en:brain calcification rajab type --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:brain calcification rajab type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  363. en:chromosome 22q11.2 microduplication syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:chromosome 22q11.2 microduplication syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  364. en:chromosome 3q29 deletion syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:chromosome 3q29 deletion syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  365. en:cleidocranial dysplasia --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:cleidocranial dysplasia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  366. en:cochleosaccular degeneration of the inner ear and progressive cataracts --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:cochleosaccular degeneration of the inner ear and progressive cataracts | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  367. en:congenital gastrointestinal-urinary tract fistula --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:congenital gastrointestinal-urinary tract fistula | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  368. en:congenital pigmentary skin anomalies --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:congenital pigmentary skin anomalies | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  369. en:conjunctival pigmentation --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:conjunctival pigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  370. en:crisponi syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:crisponi syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  371. en:dentatorubral-pallidoluysian atrophy --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:dentatorubral-pallidoluysian atrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  372. en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  373. en:diabetic truncal radiculopathy --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:diabetic truncal radiculopathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  374. en:diffuse palmoplantar keratoderma and acrocyanosis syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  375. en:epiphyseal dysplasia, multiple, 1 --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:epiphyseal dysplasia, multiple, 1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  376. en:etat criblé --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:etat criblé | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  377. en:familial hypodontia --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:familial hypodontia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  378. en:familial multiple myeloma --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:familial multiple myeloma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  379. en:familial partial lipodystrophy, type 2 --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:familial partial lipodystrophy, type 2 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  380. en:fatty acid hydroxylase-associated neurodegeneration --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:fatty acid hydroxylase-associated neurodegeneration | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  381. en:fibrodysplasia ossificans progressiva --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:fibrodysplasia ossificans progressiva | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  382. en:game friedman paradice syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:game friedman paradice syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  383. en:gingival odontogenic cyst --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:gingival odontogenic cyst | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  384. en:halal syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:halal syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  385. en:haspeslagh fryns muelenaere syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:haspeslagh fryns muelenaere syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  386. en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  387. en:hereditary gastrointestinal stromal tumor --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:hereditary gastrointestinal stromal tumor | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  388. en:hereditary peripheral neuropathy --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:hereditary peripheral neuropathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  389. en:hyaline dystrophy of bruch's membrane --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:hyaline dystrophy of bruch's membrane | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  390. en:hyperinsulinism due to uncoupling protein 2 deficiency --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  391. en:intestinal hemorrhage --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:intestinal hemorrhage | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  392. en:iron-deficiency anemia --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:iron-deficiency anemia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  393. en:juvenile amyotrophic lateral sclerosis --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:juvenile amyotrophic lateral sclerosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  394. en:leopard syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:leopard syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  395. en:linear iga bullous dermatosis --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:linear iga bullous dermatosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  396. en:malignant testicular germ cell tumor --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:malignant testicular germ cell tumor | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  397. en:melanoma astrocytoma syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:melanoma astrocytoma syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  398. en:microcephaly albinism digital anomalies syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:microcephaly albinism digital anomalies syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  399. en:microcolon --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:microcolon | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  400. en:mohr-tranebjaerg syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:mohr-tranebjaerg syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  401. en:multiple endocrine neoplasia type 1 --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:multiple endocrine neoplasia type 1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  402. en:multiple endocrine neoplasia type 2b --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:multiple endocrine neoplasia type 2b | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  403. en:multiple epiphyseal dysplasia type 5 --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:multiple epiphyseal dysplasia type 5 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  404. en:nail-patella syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:nail-patella syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  405. en:neurodegeneration with brain iron accumulation 4 --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:neurodegeneration with brain iron accumulation 4 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  406. en:okihiro syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:okihiro syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  407. en:osteogenesis imperfecta, levin type --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:osteogenesis imperfecta, levin type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  408. en:osteopenia --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:osteopenia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  409. en:ovarian carcinoma --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:ovarian carcinoma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  410. en:papillary muscle degeneration --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:papillary muscle degeneration | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  411. en:pituitary adenoma, familial isolated (disorder) --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:pituitary adenoma, familial isolated (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  412. en:post-inflammatory hyperpigmentation in lichen planus --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:post-inflammatory hyperpigmentation in lichen planus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  413. en:posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  414. en:postinflammatory hyperpigmentation --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:postinflammatory hyperpigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  415. en:potassium aggravated myotonia --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:potassium aggravated myotonia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  416. en:prickle1-related progressive myoclonus epilepsy with ataxia --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:prickle1-related progressive myoclonus epilepsy with ataxia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  417. en:radial hypoplasia, triphalangeal thumbs and hypospadias --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:radial hypoplasia, triphalangeal thumbs and hypospadias | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  418. en:ras-associated autoimmune leukoproliferative disorder --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:ras-associated autoimmune leukoproliferative disorder | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  419. en:reticulate acropigmentation of kitamura --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:reticulate acropigmentation of kitamura | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  420. en:short stature with valvular heart disease and characteristic facies syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:short stature with valvular heart disease and characteristic facies syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  421. en:sitosterolemia with xanthomatosis --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:sitosterolemia with xanthomatosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  422. en:spinocerebellar ataxia 10 --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:spinocerebellar ataxia 10 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  423. en:stk11, 1-bp del, 843g --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:stk11, 1-bp del, 843g | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  424. en:stk11, 2-bp del, nt277 --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:stk11, 2-bp del, nt277 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  425. en:stoma site polyp --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:stoma site polyp | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  426. en:tuberous sclerosis --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:tuberous sclerosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  427. en:type v acrocephalosyndactyly --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:type v acrocephalosyndactyly | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  428. en:ulna metaphyseal dysplasia syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:ulna metaphyseal dysplasia syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  429. en:ulnar-mammary syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:ulnar-mammary syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  430. en:wellesley carman french syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:wellesley carman french syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  431. en:wilms tumor-aniridia-genitourinary anomalies-mental retardation-obesity syndrome --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation-obesity syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  432. neurofibromatose de type VI --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=neurofibromatose de type VI | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  433. onycho-ostéodysostose --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=onycho-ostéodysostose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  434. sclérose tubéreuse du cerveau --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=sclérose tubéreuse du cerveau | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  435. état criblé --- r_associated #0: 35 --> en:peutz-jeghers syndrome
    n1=état criblé | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  436. Sotos (syndrome de) --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=Sotos (syndrome de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  437. en:acrocallosal syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:acrocallosal syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  438. en:allgrove syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:allgrove syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  439. en:angiokeratoma corporis diffusum --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:angiokeratoma corporis diffusum | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  440. en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  441. en:anterior displaced anus --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:anterior displaced anus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  442. en:ataxia with vitamin e deficiency --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:ataxia with vitamin e deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  443. en:autosomal dominant idiopathic familial dystonia --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant idiopathic familial dystonia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  444. en:autosomal dominant progressive nephropathy with hypertension --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant progressive nephropathy with hypertension | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  445. en:basal epidermolysis bullosa simplex --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:basal epidermolysis bullosa simplex | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  446. en:benign small intestinal neoplasm --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:benign small intestinal neoplasm | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  447. en:brachymesophalangy 2 and 5 --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:brachymesophalangy 2 and 5 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  448. en:brooke-spiegler syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:brooke-spiegler syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  449. en:centrofacial lentiginosis syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:centrofacial lentiginosis syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  450. en:cervical hypertrichosis and peripheral neuropathy syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:cervical hypertrichosis and peripheral neuropathy syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  451. en:charcot-marie-tooth disease, axonal, type 2e (disorder) --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  452. en:cockayne syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:cockayne syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  453. en:currarino triad --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:currarino triad | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  454. en:czech dysplasia, metatarsal type --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:czech dysplasia, metatarsal type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  455. en:demyelinating polyneuropathy --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:demyelinating polyneuropathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  456. en:enterokinase deficiency --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:enterokinase deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  457. en:eyelid xanthoma --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:eyelid xanthoma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  458. en:familial amyloid polyneuropathy with cutaneous amyloidosis --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:familial amyloid polyneuropathy with cutaneous amyloidosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  459. en:familial chronic lymphocytic leukemia --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:familial chronic lymphocytic leukemia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  460. en:familial creutzfeldt-jakob --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:familial creutzfeldt-jakob | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  461. en:familial neuroblastoma --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:familial neuroblastoma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  462. en:ferro-cerebro-cutaneous syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:ferro-cerebro-cutaneous syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  463. en:generalized epilepsy and paroxysmal dyskinesia syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:generalized epilepsy and paroxysmal dyskinesia syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  464. en:generalized peeling skin syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:generalized peeling skin syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  465. en:gerstmann-straussler-scheinker disease --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:gerstmann-straussler-scheinker disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  466. en:glycogen storage disease 0, liver --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:glycogen storage disease 0, liver | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  467. en:goniodysgenesis-mental retardation-short stature syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  468. en:hawkinsinuria --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:hawkinsinuria | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  469. en:hereditary cerebellar atrophy --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:hereditary cerebellar atrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  470. en:hereditary cystatin c amyloid angiopathy --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:hereditary cystatin c amyloid angiopathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  471. en:hereditary lesion --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:hereditary lesion | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  472. en:hereditary non-polyposis colorectal cancer syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:hereditary non-polyposis colorectal cancer syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  473. en:holoprosencephaly with fetal akinesia-hypokinesia sequence --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  474. en:hyaline body --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:hyaline body | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  475. en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  476. en:insulin growth factor i deficiency --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:insulin growth factor i deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  477. en:kernicterus --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:kernicterus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  478. en:lentigo --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:lentigo | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  479. en:lissencephaly type 3 familial fetal akinesia sequence syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  480. en:macular pigment deposit --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:macular pigment deposit | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  481. en:metaphyseal dysplasia, braun-tinschert type --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:metaphyseal dysplasia, braun-tinschert type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  482. en:microphthalmia, syndromic 3 --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:microphthalmia, syndromic 3 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  483. en:muckle-wells syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:muckle-wells syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  484. en:multiple endocrine neoplasia --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:multiple endocrine neoplasia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  485. en:neurofibromatosis, type 1-like syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:neurofibromatosis, type 1-like syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  486. en:neuropathy, hereditary motor and sensory, okinawa type --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:neuropathy, hereditary motor and sensory, okinawa type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  487. en:non-polyposis turcot syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:non-polyposis turcot syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  488. en:other specified congenital malformations of upper alimentary tract --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:other specified congenital malformations of upper alimentary tract | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  489. en:pancreatic triacylglycerol lipase deficiency --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:pancreatic triacylglycerol lipase deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  490. en:papillon-lefevre syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:papillon-lefevre syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  491. en:parietal foramina --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:parietal foramina | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  492. en:partington x-linked mental retardation syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:partington x-linked mental retardation syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  493. en:pericarditis due to deposits of cholesterol --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:pericarditis due to deposits of cholesterol | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  494. en:pitted keratolysis --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:pitted keratolysis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  495. en:polydactyly, preaxial ii (disorder) --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:polydactyly, preaxial ii (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  496. en:reis-bucklers' corneal dystrophy --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:reis-bucklers' corneal dystrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  497. en:schindler disease, type i --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:schindler disease, type i | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  498. en:simpson golabi behmel syndrome type 1 --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:simpson golabi behmel syndrome type 1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  499. en:spinocerebellar ataxia 29 --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:spinocerebellar ataxia 29 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  500. en:spinocerebellar ataxia type 32 --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:spinocerebellar ataxia type 32 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  501. en:spinocerebellar ataxia type 6 (disorder) --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:spinocerebellar ataxia type 6 (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  502. en:split-hand-foot malformation with long bone deficiency 1 --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:split-hand-foot malformation with long bone deficiency 1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  503. en:strudwick syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:strudwick syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  504. en:timothy syndrome type 2 --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:timothy syndrome type 2 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  505. en:transthyretin related familial amyloid cardiomyopathy --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:transthyretin related familial amyloid cardiomyopathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  506. en:vascular neurocutaneous syndrome --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=en:vascular neurocutaneous syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  507. goniodysgénésie-retard mental-petite taille (syndrome) --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=goniodysgénésie-retard mental-petite taille (syndrome) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  508. ictère nucléaire --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=ictère nucléaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  509. lentiginose périorificielle avec polypose viscérale --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=lentiginose périorificielle avec polypose viscérale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  510. lipofuscinose neuronale céroïde infantile finlandaise --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=lipofuscinose neuronale céroïde infantile finlandaise | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  511. mélanodermite toxique d'Hoffmann-Habermann --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=mélanodermite toxique d'Hoffmann-Habermann | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  512. nævus dysplasique (syndrome du) --- r_associated #0: 34 --> en:peutz-jeghers syndrome
    n1=nævus dysplasique (syndrome du) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=34
  513. bran de Judas --- r_associated #0: 33 --> en:peutz-jeghers syndrome
    n1=bran de Judas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=33
  514. dystrophie vulvaire --- r_associated #0: 33 --> en:peutz-jeghers syndrome
    n1=dystrophie vulvaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=33
  515. en:hereditary stomatocytosis --- r_associated #0: 33 --> en:peutz-jeghers syndrome
    n1=en:hereditary stomatocytosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=33
  516. fibromatose gingivale --- r_associated #0: 33 --> en:peutz-jeghers syndrome
    n1=fibromatose gingivale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=33
  517. kératolyse ponctuée --- r_associated #0: 33 --> en:peutz-jeghers syndrome
    n1=kératolyse ponctuée | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=33
  518. Syndrome de Marfan --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=Syndrome de Marfan | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  519. en:Soto's syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:Soto's syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  520. en:angina co-occurrent and due to arteriosclerosis of coronary artery bypass graft --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:angina co-occurrent and due to arteriosclerosis of coronary artery bypass graft | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  521. en:application site pigmentation changes --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:application site pigmentation changes | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  522. en:ataxia telangiectasia syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:ataxia telangiectasia syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  523. en:atrophy of vulva --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:atrophy of vulva | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  524. en:autosomal dominant focal dystonia dyt25 type --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant focal dystonia dyt25 type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  525. en:autosomal dominant ichthyosis --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant ichthyosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  526. en:autosomal dominant mutilating keratoderma --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant mutilating keratoderma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  527. en:behr syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:behr syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  528. en:benign lymphoid polyposis of intestine --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:benign lymphoid polyposis of intestine | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  529. en:cerebral lipidosis --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:cerebral lipidosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  530. en:charcot-marie-tooth disease, axonal, type 2b (disorder) --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  531. en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  532. en:cole disease --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:cole disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  533. en:congenital anomaly of esophagus --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:congenital anomaly of esophagus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  534. en:congenital anomaly of intestinal tract --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:congenital anomaly of intestinal tract | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  535. en:congenital reticular ichthyosiform erythroderma --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:congenital reticular ichthyosiform erythroderma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  536. en:corneal dystrophy, congenital stromal --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:corneal dystrophy, congenital stromal | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  537. en:crigler-najjar syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:crigler-najjar syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  538. en:crouzon syndrome with acanthosis nigricans (disorder) --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  539. en:demyelinating disorder of central nervous system --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:demyelinating disorder of central nervous system | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  540. en:dysplasia, saddan --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:dysplasia, saddan | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  541. en:ehlers-danlos syndrome vascular-like type --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:ehlers-danlos syndrome vascular-like type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  542. en:emberger syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:emberger syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  543. en:familial osteochondritis dissecans --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:familial osteochondritis dissecans | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  544. en:familial papillary thyroid carcinoma with renal papillary neoplasia syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:familial papillary thyroid carcinoma with renal papillary neoplasia syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  545. en:feingold syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:feingold syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  546. en:fragile x tremor/ataxia syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:fragile x tremor/ataxia syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  547. en:gastrointestinal vessel anomaly --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:gastrointestinal vessel anomaly | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  548. en:geniospasm 1 --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:geniospasm 1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  549. en:hamartoma of small intestine --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:hamartoma of small intestine | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  550. en:hereditary angioedema --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:hereditary angioedema | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  551. en:hereditary non polyposis colorectal cancer --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:hereditary non polyposis colorectal cancer | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  552. en:hyperpigmented spots on hands (especially palms), arms, feet (especially plantar areas), legs, and lips --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:hyperpigmented spots on hands (especially palms), arms, feet (especially plantar areas), legs, and lips | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  553. en:hyperuricemia, anemia, renal failure syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:hyperuricemia, anemia, renal failure syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  554. en:hypopigmentation of eyelid --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:hypopigmentation of eyelid | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  555. en:imperforate anus --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:imperforate anus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  556. en:intestinal cyst --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:intestinal cyst | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  557. en:juvenile osteochondrosis of hand --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:juvenile osteochondrosis of hand | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  558. en:labial lentigo --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:labial lentigo | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  559. en:lamellar ichthyosis, autosomal dominant form --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:lamellar ichthyosis, autosomal dominant form | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  560. en:large intestinal polyposis --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:large intestinal polyposis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  561. en:li-fraumeni syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:li-fraumeni syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  562. en:malignant thyroid gland neoplasm --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:malignant thyroid gland neoplasm | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  563. en:melnick-fraser syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:melnick-fraser syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  564. en:microbiological --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:microbiological | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  565. en:microcephaly deafness syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:microcephaly deafness syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  566. en:microcephaly microcornea syndrome seemanova type --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:microcephaly microcornea syndrome seemanova type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  567. en:mousa al din al nassar syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:mousa al din al nassar syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  568. en:mowat-wilson syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:mowat-wilson syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  569. en:multiple endocrine neoplasia type 2a --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:multiple endocrine neoplasia type 2a | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  570. en:north american indian childhood cirrhosis --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:north american indian childhood cirrhosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  571. en:odontoma dysphagia syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:odontoma dysphagia syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  572. en:pancreas cancer --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:pancreas cancer | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  573. en:panniculitis due to hyperuricemia --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:panniculitis due to hyperuricemia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  574. en:peeling skin syndrome, acral type --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:peeling skin syndrome, acral type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  575. en:peutz-jeghers polyp of the small intestine --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:peutz-jeghers polyp of the small intestine | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  576. en:pigment dispersion syndrome of bilateral eyes --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:pigment dispersion syndrome of bilateral eyes | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  577. en:pigmentation changes nec --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:pigmentation changes nec | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  578. en:piussan lenaerts mathieu syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:piussan lenaerts mathieu syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  579. en:posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  580. en:postinflammatory skin pigmentation change --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:postinflammatory skin pigmentation change | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  581. en:scleroderma-associated hypermelanosis --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:scleroderma-associated hypermelanosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  582. en:shprintzen omphalocele syndrome --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:shprintzen omphalocele syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  583. en:spinocerebellar ataxia type 37 --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:spinocerebellar ataxia type 37 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  584. en:spondylocostal dysostosis 4, autosomal dominant --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:spondylocostal dysostosis 4, autosomal dominant | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  585. en:sting-associated vasculopathy with onset in infancy --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:sting-associated vasculopathy with onset in infancy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  586. en:stk11 gene --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:stk11 gene | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  587. en:stk11, 1-bp del, 1407c --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:stk11, 1-bp del, 1407c | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  588. en:stk11, 4-bp del, 716ggtc --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:stk11, 4-bp del, 716ggtc | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  589. en:stk11, leu67pro --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:stk11, leu67pro | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  590. en:type Went --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:type Went | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  591. en:vulvar dystrophy --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:vulvar dystrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  592. en:xanthoma of lung --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=en:xanthoma of lung | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  593. imperforation de l'anus --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=imperforation de l'anus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  594. microbiologique --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=microbiologique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  595. nævomatose basocellulaire multiple --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=nævomatose basocellulaire multiple | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  596. ongles jaunes (syndrome des) --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=ongles jaunes (syndrome des) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  597. épidémiologique --- r_associated #0: 32 --> en:peutz-jeghers syndrome
    n1=épidémiologique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32
  598. adénomatose rectocolique familiale --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=adénomatose rectocolique familiale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  599. dysplasie acromicrique --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=dysplasie acromicrique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  600. en:acquired hypopigmentation of choroid --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:acquired hypopigmentation of choroid | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  601. en:acquired lentiginosis --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:acquired lentiginosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  602. en:acro-dermato-ungual-lacrimal-tooth syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:acro-dermato-ungual-lacrimal-tooth syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  603. en:allan-herndon-dudley syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:allan-herndon-dudley syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  604. en:aspects of mortality statistics --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:aspects of mortality statistics | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  605. en:atrophia --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:atrophia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  606. en:atrophic myositis --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:atrophic myositis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  607. en:atrophy of salivary gland --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:atrophy of salivary gland | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  608. en:attenuated familial adenomatous polyposis --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:attenuated familial adenomatous polyposis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  609. en:autosomal dominant pterygium of conjunctiva --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant pterygium of conjunctiva | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  610. en:autosomal recessive primary microcephaly --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:autosomal recessive primary microcephaly | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  611. en:behrens baumann dust syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:behrens baumann dust syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  612. en:birt-hogg-dube syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:birt-hogg-dube syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  613. en:centronuclear myopathy 1 --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:centronuclear myopathy 1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  614. en:cerebral cavernous malformation --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:cerebral cavernous malformation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  615. en:choledochal cyst --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:choledochal cyst | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  616. en:chromosome 17q21.31 deletion syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:chromosome 17q21.31 deletion syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  617. en:complication aspects --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:complication aspects | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  618. en:congenital duplication of appendix --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:congenital duplication of appendix | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  619. en:congenital neutropenia --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:congenital neutropenia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  620. en:congenital syphilitic mucous patches --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:congenital syphilitic mucous patches | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  621. en:constitutional mismatch repair deficiency syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:constitutional mismatch repair deficiency syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  622. en:deafness-craniofacial syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:deafness-craniofacial syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  623. en:degenerative disorder of eye --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:degenerative disorder of eye | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  624. en:denys-drash syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:denys-drash syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  625. en:dominant beta-thalassemia --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:dominant beta-thalassemia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  626. en:dysplastic nevus syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:dysplastic nevus syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  627. en:enteric duplication --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:enteric duplication | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  628. en:epiphyseal dysplasia, multiple, 2 --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:epiphyseal dysplasia, multiple, 2 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  629. en:ethnologic --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:ethnologic | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  630. en:familial isolated hyperparathyroidism --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:familial isolated hyperparathyroidism | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  631. en:familial spontaneous pneumothorax --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:familial spontaneous pneumothorax | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  632. en:freckles --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:freckles | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  633. en:frontotemporal dementia, chromosome 3-linked --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:frontotemporal dementia, chromosome 3-linked | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  634. en:hand foot uterus syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:hand foot uterus syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  635. en:hereditary gastrogenic lactose intolerance --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:hereditary gastrogenic lactose intolerance | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  636. en:hereditary gingival fibromatosis --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:hereditary gingival fibromatosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  637. en:hereditary motor and sensory-neuropathy type ii --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:hereditary motor and sensory-neuropathy type ii | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  638. en:hereditary sensory and autonomic neuropathy type 1b --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:hereditary sensory and autonomic neuropathy type 1b | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  639. en:hunter syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:hunter syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  640. en:hyperpigmentation, familial progressive --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:hyperpigmentation, familial progressive | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  641. en:intraductal papillary mucinous neoplasm --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:intraductal papillary mucinous neoplasm | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  642. en:irregular hyperpigmentation --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:irregular hyperpigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  643. en:keratosis palmoplantaris papulosa --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:keratosis palmoplantaris papulosa | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  644. en:large plaque parapsoriasis --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:large plaque parapsoriasis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  645. en:leukotriene c4 synthase deficiency --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:leukotriene c4 synthase deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  646. en:lissencephaly, x-linked, 2 --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:lissencephaly, x-linked, 2 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  647. en:microcephalic primordial dwarfism toriello type --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:microcephalic primordial dwarfism toriello type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  648. en:microcephaly-capillary malformation syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  649. en:microvillus inclusion disease --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:microvillus inclusion disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  650. en:mosaic variegated aneuploidy syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:mosaic variegated aneuploidy syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  651. en:multiple endocrine neoplasia type 2A --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:multiple endocrine neoplasia type 2A | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  652. en:myopathy, distal 2 --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:myopathy, distal 2 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  653. en:naxos disease --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:naxos disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  654. en:other phakomatoses, not elsewhere classified in icd10cm --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:other phakomatoses, not elsewhere classified in icd10cm | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  655. en:persistent acantholytic dermatosis of fawcett and miller --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:persistent acantholytic dermatosis of fawcett and miller | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  656. en:peutz-jeghers polyp --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:peutz-jeghers polyp | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  657. en:pigmentation disorder of lip --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:pigmentation disorder of lip | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  658. en:scholte syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:scholte syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  659. en:skin hypopigmentation --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:skin hypopigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  660. en:spinocerebellar ataxia 8 --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:spinocerebellar ataxia 8 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  661. en:stk11, 9-bp del --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:stk11, 9-bp del | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  662. en:stk11, glu57ter --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:stk11, glu57ter | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  663. en:syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  664. en:syndrome, branchio-oculo-facial --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:syndrome, branchio-oculo-facial | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  665. en:turcot syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:turcot syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  666. en:tylosis with esophageal cancer --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:tylosis with esophageal cancer | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  667. en:vitelliform macular dystrophy --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:vitelliform macular dystrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  668. en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  669. hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  670. migraine hémiplégique familiale --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=migraine hémiplégique familiale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  671. neurofibromatose --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=neurofibromatose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  672. ostéopénie --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=ostéopénie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  673. phlébosclérose --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=phlébosclérose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  674. polypose familiale du côlon --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=polypose familiale du côlon | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  675. polypose hamartomateuse intestinale --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=polypose hamartomateuse intestinale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  676. polypose intestinale pigmentation cutanée --- r_associated #0: 31 --> en:peutz-jeghers syndrome
    n1=polypose intestinale pigmentation cutanée | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  677. Maladie congénitale --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=Maladie congénitale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  678. Syndrome d'Alagille --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=Syndrome d'Alagille | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  679. Syndrome de Gorlin --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=Syndrome de Gorlin | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  680. Syndrome de Peutz-Jeghers --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=Syndrome de Peutz-Jeghers | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  681. Vestige du conduit vitellin --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=Vestige du conduit vitellin | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  682. anémie ferriprive --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=anémie ferriprive | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  683. atrophie optique polyneuropathie et surdité --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=atrophie optique polyneuropathie et surdité | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  684. atrophie optique-paraplégie spastique --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=atrophie optique-paraplégie spastique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  685. démence fronto-temporale --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=démence fronto-temporale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  686. démence frontotemporale --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=démence frontotemporale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  687. en:17q11.2 microduplication syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:17q11.2 microduplication syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  688. en:Dubin-Johnson's syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:Dubin-Johnson's syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  689. en:abdominal wall neoplasm benign --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:abdominal wall neoplasm benign | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  690. en:absence of fingerprints with congenital milia syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:absence of fingerprints with congenital milia syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  691. en:alagille syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:alagille syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  692. en:alpha-fetoprotein, hereditary persistence of --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:alpha-fetoprotein, hereditary persistence of | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  693. en:arsenic-induced skin pigmentation --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:arsenic-induced skin pigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  694. en:arthrogryposis, distal, type 1 --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:arthrogryposis, distal, type 1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  695. en:aspects of radionuclide imaging --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:aspects of radionuclide imaging | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  696. en:atrophoderma --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:atrophoderma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  697. en:atrophy of pancreas --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:atrophy of pancreas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  698. en:atrophy of vagina --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:atrophy of vagina | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  699. en:autosomal dominant analbuminemia --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant analbuminemia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  700. en:autosomal dominant deficiency of plasminogen --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant deficiency of plasminogen | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  701. en:autosomal dominant optic atrophy --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant optic atrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  702. en:bannayan syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:bannayan syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  703. en:bituminosis --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:bituminosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  704. en:brachydactyly, type a1 (disorder) --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:brachydactyly, type a1 (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  705. en:breast carcinoma --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:breast carcinoma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  706. en:carney complex --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:carney complex | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  707. en:carney-stratakis syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:carney-stratakis syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  708. en:charcot-marie-tooth disease type 2d --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:charcot-marie-tooth disease type 2d | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  709. en:charcot-marie-tooth disease, type 2j --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:charcot-marie-tooth disease, type 2j | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  710. en:cloacal exstrophy --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:cloacal exstrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  711. en:cone-dystrophy --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:cone-dystrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  712. en:costello syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:costello syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  713. en:craniofacial deafness hand syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:craniofacial deafness hand syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  714. en:craniosynostosis with facial dysmorphism and brachydactyly syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  715. en:cutis laxa, autosomal recessive --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:cutis laxa, autosomal recessive | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  716. en:deafness --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:deafness | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  717. en:developmental absence of tooth --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:developmental absence of tooth | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  718. en:developmental fault --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:developmental fault | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  719. en:dystrophia myotonica 2 --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:dystrophia myotonica 2 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  720. en:familial acute myeloid leukemia --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:familial acute myeloid leukemia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  721. en:familial amyloid neuropathy --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:familial amyloid neuropathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  722. en:familial waldenstrom macroglobulinemia --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:familial waldenstrom macroglobulinemia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  723. en:fatal familial insomnia --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:fatal familial insomnia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  724. en:frontotemporal dementia --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:frontotemporal dementia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  725. en:genital lichen sclerosus --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:genital lichen sclerosus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  726. en:hall riggs syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:hall riggs syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  727. en:hereditary diffuse gastric adenocarcinoma --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:hereditary diffuse gastric adenocarcinoma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  728. en:hereditary motor and sensory neuropathy type i --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:hereditary motor and sensory neuropathy type i | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  729. en:hereditary motor neuron disease --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:hereditary motor neuron disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  730. en:hereditary multiple ossifying ecchondromata --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:hereditary multiple ossifying ecchondromata | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  731. en:hereditary myopathy with early respiratory failure --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:hereditary myopathy with early respiratory failure | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  732. en:hereditary paraganglioma-pheochromocytoma syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:hereditary paraganglioma-pheochromocytoma syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  733. en:hereditary systemic amyloidosis --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:hereditary systemic amyloidosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  734. en:hnsha due to triosephosphate isomerase deficiency --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:hnsha due to triosephosphate isomerase deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  735. en:hyperinsulinemic hypoglycemia, familial, 7 --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:hyperinsulinemic hypoglycemia, familial, 7 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  736. en:hypermelanosis due to hodgkin's disease --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:hypermelanosis due to hodgkin's disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  737. en:hyperparathyroidism-jaw tumor syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:hyperparathyroidism-jaw tumor syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  738. en:hypotrichosis simplex of scalp --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:hypotrichosis simplex of scalp | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  739. en:inherited cutaneous hyperpigmentation --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:inherited cutaneous hyperpigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  740. en:intestinal lipofuscinosis --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:intestinal lipofuscinosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  741. en:liddle syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:liddle syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  742. en:lynch syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:lynch syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  743. en:macerated stillbirth --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:macerated stillbirth | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  744. en:marasmus --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:marasmus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  745. en:mee's line --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:mee's line | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  746. en:melanodermatitis toxica lichenoides --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:melanodermatitis toxica lichenoides | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  747. en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  748. en:metaplastic polyposis of intestine --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:metaplastic polyposis of intestine | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  749. en:microcornea with glaucoma and absent frontal sinus syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:microcornea with glaucoma and absent frontal sinus syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  750. en:muir-torre syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:muir-torre syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  751. en:muller-weiss disease --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:muller-weiss disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  752. en:myomalacia --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:myomalacia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  753. en:myopathy, distal, tateyama type --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:myopathy, distal, tateyama type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  754. en:persistent cloaca --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:persistent cloaca | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  755. en:pontocerebellar hypoplasia type 2 --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:pontocerebellar hypoplasia type 2 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  756. en:porphyria --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:porphyria | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  757. en:premature aging syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:premature aging syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  758. en:primary pigmented nodular adrenocortical disease --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:primary pigmented nodular adrenocortical disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  759. en:pseudocholinesterase deficiency --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:pseudocholinesterase deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  760. en:pulmonary alveolar proteinosis, acquired --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:pulmonary alveolar proteinosis, acquired | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  761. en:rothmund-thomson syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:rothmund-thomson syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  762. en:short fifth metacarpal insulin resistance syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:short fifth metacarpal insulin resistance syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  763. en:spinocerebellar ataxia 28 --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:spinocerebellar ataxia 28 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  764. en:spinocerebellar ataxia 31 (disorder) --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:spinocerebellar ataxia 31 (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  765. en:spinocerebellar ataxia type 5 --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:spinocerebellar ataxia type 5 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  766. en:steinfeld syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:steinfeld syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  767. en:stk11 wt allele --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:stk11 wt allele | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  768. en:stk11, 1-bp ins, 535t --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:stk11, 1-bp ins, 535t | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  769. en:stk11, tyr253ter --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:stk11, tyr253ter | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  770. en:trichohepatoenteric syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:trichohepatoenteric syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  771. en:tylosis --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:tylosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  772. en:vitiligo iridis --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:vitiligo iridis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  773. en:von hippel-lindau syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:von hippel-lindau syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  774. en:zimmerman laband syndrome --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=en:zimmerman laband syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  775. tylosis --- r_associated #0: 30 --> en:peutz-jeghers syndrome
    n1=tylosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=30
  776. NEM 2B ou 3 --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=NEM 2B ou 3 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  777. albinisme oculocutané de type mutant jaune --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=albinisme oculocutané de type mutant jaune | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  778. atrophie optique, surdité, épilepsie, spasticité et décès précoce --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=atrophie optique, surdité, épilepsie, spasticité et décès précoce | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  779. en:2-hydroxyglutaric aciduria --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:2-hydroxyglutaric aciduria | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  780. en:aase syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:aase syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  781. en:acromicric dysplasia --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:acromicric dysplasia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  782. en:aicardi syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:aicardi syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  783. en:ameloonychohypohidrotic syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:ameloonychohypohidrotic syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  784. en:arterial dissection and lentiginosis syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:arterial dissection and lentiginosis syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  785. en:atrophic fibrosis of lung --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:atrophic fibrosis of lung | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  786. en:autosomal dominant charcot-marie-tooth disease type 2c --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant charcot-marie-tooth disease type 2c | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  787. en:beare-stevenson cutis gyrata syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:beare-stevenson cutis gyrata syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  788. en:benign colorectal neoplasm --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:benign colorectal neoplasm | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  789. en:bethlem myopathy 1 --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:bethlem myopathy 1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  790. en:chronic diarrhea with villous atrophy syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:chronic diarrhea with villous atrophy syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  791. en:cleft lip/palate-ectodermal dysplasia syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:cleft lip/palate-ectodermal dysplasia syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  792. en:cleidorhizomelic syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:cleidorhizomelic syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  793. en:cobb syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:cobb syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  794. en:congenital osteodystrophy --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:congenital osteodystrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  795. en:duodenal atresia --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:duodenal atresia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  796. en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:ectodermal dysplasia with blindness syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  797. en:ectodermal dysplasia with natal teeth, turnpenny type --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:ectodermal dysplasia with natal teeth, turnpenny type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  798. en:epilepsy, myoclonic, benign adult familial, type 2 --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:epilepsy, myoclonic, benign adult familial, type 2 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  799. en:eyelash hyperpigmentation --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:eyelash hyperpigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  800. en:familial chronic pancreatitis --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:familial chronic pancreatitis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  801. en:familial encephalopathy with neuroserpin inclusion bodies --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:familial encephalopathy with neuroserpin inclusion bodies | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  802. en:familial isolated arrhythmogenic right ventricular dysplasia --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:familial isolated arrhythmogenic right ventricular dysplasia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  803. en:familial malignant melanoma of skin --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:familial malignant melanoma of skin | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  804. en:familial non-medullary thyroid cancer --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:familial non-medullary thyroid cancer | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  805. en:farber lipogranulomatosis --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:farber lipogranulomatosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  806. en:gastrointestinal premalignant disorders (smq) --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:gastrointestinal premalignant disorders (smq) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  807. en:glomuvenous malformations --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:glomuvenous malformations | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  808. en:hemiatrophy of lower limb --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:hemiatrophy of lower limb | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  809. en:hereditary cerebellar degeneration --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:hereditary cerebellar degeneration | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  810. en:hereditary mucosal leukokeratosis --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:hereditary mucosal leukokeratosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  811. en:hereditary neoplastic syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:hereditary neoplastic syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  812. en:hereditary optic atrophy --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:hereditary optic atrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  813. en:heritable pulmonary arterial hypertension due to bmpr2 mutation --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  814. en:hyperferritinemia, hereditary, with congenital cataracts --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:hyperferritinemia, hereditary, with congenital cataracts | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  815. en:hyperinsulinism due to insulin receptor deficiency --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:hyperinsulinism due to insulin receptor deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  816. en:hyperpigmented macules of buccal mucosa --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:hyperpigmented macules of buccal mucosa | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  817. en:hypohidrosis due to genetic abnormality of eccrine gland structure and function --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:hypohidrosis due to genetic abnormality of eccrine gland structure and function | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  818. en:ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  819. en:intestinal malrotation --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:intestinal malrotation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  820. en:intestinal polyposis --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:intestinal polyposis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  821. en:menkes disease --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:menkes disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  822. en:mesomelic dwarfism reinhardt pfeiffer type --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:mesomelic dwarfism reinhardt pfeiffer type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  823. en:microcephaly cervical spine fusion anomalies --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:microcephaly cervical spine fusion anomalies | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  824. en:microcephaly, amish type (disorder) --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:microcephaly, amish type (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  825. en:mobile caecum syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:mobile caecum syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  826. en:mucous patch of oral mucosa --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:mucous patch of oral mucosa | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  827. en:nance-horan syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:nance-horan syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  828. en:neuronal intestinal pseudoobstruction --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:neuronal intestinal pseudoobstruction | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  829. en:otoonychoperoneal syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:otoonychoperoneal syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  830. en:palmoplantar porokeratosis --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:palmoplantar porokeratosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  831. en:periorificial lentiginosis --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:periorificial lentiginosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  832. en:pharmacotherapeutic --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:pharmacotherapeutic | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  833. en:phlebosclerosis --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:phlebosclerosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  834. en:poikiloderma of civatte --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:poikiloderma of civatte | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  835. en:poikiloderma, hereditary sclerosing --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:poikiloderma, hereditary sclerosing | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  836. en:potocki-shaffer syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:potocki-shaffer syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  837. en:rhabdoid tumor predisposition syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:rhabdoid tumor predisposition syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  838. en:rhinitis, atrophic --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:rhinitis, atrophic | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  839. en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  840. en:stk11, ex4-5del/ex6-7inv --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:stk11, ex4-5del/ex6-7inv | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  841. en:stk11, lys84ter --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:stk11, lys84ter | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  842. en:stk11, trp239cys --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:stk11, trp239cys | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  843. en:transposition of intestine (disorder) --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:transposition of intestine (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  844. en:type i acrocephalosyndactyly --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:type i acrocephalosyndactyly | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  845. en:vacterl association --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:vacterl association | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  846. en:vulval melanotic macule --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:vulval melanotic macule | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  847. en:x-linked dystonia parkinsonism --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:x-linked dystonia parkinsonism | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  848. en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  849. syndrome de Peutz-Touraine-Jeghers --- r_associated #0: 29 --> en:peutz-jeghers syndrome
    n1=syndrome de Peutz-Touraine-Jeghers | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=29
  850. acrodermatitis enteropathica --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=acrodermatitis enteropathica | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  851. atrophie optique congénitale ou infantile précoce --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=atrophie optique congénitale ou infantile précoce | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  852. atrophie optique tardive liée au sexe --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=atrophie optique tardive liée au sexe | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  853. contractures congénitales et arachnodactylie --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=contractures congénitales et arachnodactylie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  854. en:Dubin-Sprinz disease --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:Dubin-Sprinz disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  855. en:Feingold syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:Feingold syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  856. en:arachnodactily --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:arachnodactily | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  857. en:argyria --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:argyria | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  858. en:autosomal dominant beta2-microglobulinic amyloidosis --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant beta2-microglobulinic amyloidosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  859. en:behavioral variant of frontotemporal dementia --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:behavioral variant of frontotemporal dementia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  860. en:birth mark --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:birth mark | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  861. en:blau syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:blau syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  862. en:brachytelephalangy, facial dysmorphism, kallmann syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  863. en:cerebroretinal microangiopathy with calcifications and cysts (disorder) --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  864. en:charcot-marie-tooth disease, axonal, type 2l (disorder) --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  865. en:choreoathetosis/spasticity, episodic --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:choreoathetosis/spasticity, episodic | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  866. en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  867. en:corneal dystrophy, subepithelial mucinous --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:corneal dystrophy, subepithelial mucinous | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  868. en:crystal arthropathy --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:crystal arthropathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  869. en:degenerative and/or vascular disorder of ear --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:degenerative and/or vascular disorder of ear | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  870. en:dicer1 syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:dicer1 syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  871. en:discrete intestinal polyps --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:discrete intestinal polyps | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  872. en:dyschondrosteosis and nephritis syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:dyschondrosteosis and nephritis syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  873. en:dyskeratosis congenita, autosomal dominant --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:dyskeratosis congenita, autosomal dominant | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  874. en:dystonia 12 --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:dystonia 12 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  875. en:encephalopathy due to sulfite oxidase deficiency --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:encephalopathy due to sulfite oxidase deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  876. en:epidemiological --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:epidemiological | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  877. en:epithelial recurrent erosion dystrophy --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:epithelial recurrent erosion dystrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  878. en:familial benign neonatal epilepsy --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:familial benign neonatal epilepsy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  879. en:familial hemiplegic migraine --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:familial hemiplegic migraine | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  880. en:fanconi anemia --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:fanconi anemia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  881. en:follicular atrophoderma and basal cell epitheliomata --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:follicular atrophoderma and basal cell epitheliomata | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  882. en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  883. en:gastric hemangioma --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:gastric hemangioma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  884. en:gastrointestinal neoplasms benign nec --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:gastrointestinal neoplasms benign nec | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  885. en:hereditary cerebral amyloid angiopathy, icelandic type --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:hereditary cerebral amyloid angiopathy, icelandic type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  886. en:hereditary leiomyomatosis and renal cell cancer --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:hereditary leiomyomatosis and renal cell cancer | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  887. en:hereditary thyroid gland medullary carcinoma --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:hereditary thyroid gland medullary carcinoma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  888. en:hypomyelination and congenital cataract --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:hypomyelination and congenital cataract | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  889. en:inherited bone marrow failure syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:inherited bone marrow failure syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  890. en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  891. en:iris coloboma with ptosis, hypertelorism, and mental retardation --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:iris coloboma with ptosis, hypertelorism, and mental retardation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  892. en:keratoacanthoma familial --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:keratoacanthoma familial | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  893. en:lentigo - freckle --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:lentigo - freckle | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  894. en:lesion of degenerative abnormality --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:lesion of degenerative abnormality | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  895. en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  896. en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  897. en:masa syndrome (disorder) --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:masa syndrome (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  898. en:melanocytic hyperplasia --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:melanocytic hyperplasia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  899. en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  900. en:morava mehes syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:morava mehes syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  901. en:mottled pigmentation --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:mottled pigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  902. en:moyamoya disease with early onset achalasia --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:moyamoya disease with early onset achalasia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  903. en:multiple gastrointestinal atresias (disorder) --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:multiple gastrointestinal atresias (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  904. en:necrotic process --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:necrotic process | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  905. en:neurofibromatosis type 2 --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:neurofibromatosis type 2 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  906. en:neuronal intestinal dysplasia --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:neuronal intestinal dysplasia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  907. en:nicolaides baraitser syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:nicolaides baraitser syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  908. en:ocular albinism-lentigines-deafness syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:ocular albinism-lentigines-deafness syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  909. en:ohdo syndrome, maat-kievit-brunner type --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:ohdo syndrome, maat-kievit-brunner type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  910. en:other specified congenital malformations of digestive system --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:other specified congenital malformations of digestive system | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  911. en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  912. en:pancreatic cyst rupture --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:pancreatic cyst rupture | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  913. en:pili torti-deafness syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:pili torti-deafness syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  914. en:pituitary thyroid hormone resistance --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:pituitary thyroid hormone resistance | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  915. en:polyposis coli --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:polyposis coli | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  916. en:pterygium colli mental retardation digital anomalies --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:pterygium colli mental retardation digital anomalies | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  917. en:roch leri mesosomatous lipomatosis --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:roch leri mesosomatous lipomatosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  918. en:schambergs disease --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:schambergs disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  919. en:schopf-schulz-passarge syndrome (disorder) --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:schopf-schulz-passarge syndrome (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  920. en:spinocerebellar ataxia 1s --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:spinocerebellar ataxia 1s | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  921. en:spinocerebellar ataxia 36 --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:spinocerebellar ataxia 36 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  922. en:spinocerebellar ataxia type 7 --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:spinocerebellar ataxia type 7 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  923. en:synpolydactyly --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:synpolydactyly | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  924. en:tarsal-carpal coalition syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:tarsal-carpal coalition syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  925. en:tubular renal disease with cardiomyopathy syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:tubular renal disease with cardiomyopathy syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  926. en:tyrosinemia type i --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:tyrosinemia type i | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  927. en:vestigial gastrointestinal remnant --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:vestigial gastrointestinal remnant | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  928. en:waisman syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:waisman syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  929. en:wiskott-aldrich syndrome --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:wiskott-aldrich syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  930. en:x-linked lissencephaly --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:x-linked lissencephaly | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  931. en:zosteriform reticulate hyperpigmentation --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=en:zosteriform reticulate hyperpigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  932. microdélétion 5q35 --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=microdélétion 5q35 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  933. mélanodermite toxique --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=mélanodermite toxique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  934. radiographique --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=radiographique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  935. une anomalie congénitale --- r_associated #0: 28 --> en:peutz-jeghers syndrome
    n1=une anomalie congénitale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=28
  936. agranulocytose constitutionnelle --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=agranulocytose constitutionnelle | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  937. atrophie optique --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=atrophie optique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  938. diverticule de meckel --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=diverticule de meckel | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  939. dépigmentation --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=dépigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  940. en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  941. en:atrophy of soft tissue of orbit --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:atrophy of soft tissue of orbit | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  942. en:autosomal recessive idiopathic familial dystonia --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:autosomal recessive idiopathic familial dystonia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  943. en:benign autosomal dominant osteopetrosis --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:benign autosomal dominant osteopetrosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  944. en:benign digestive system neoplasm --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:benign digestive system neoplasm | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  945. en:benign peritoneal neoplasm --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:benign peritoneal neoplasm | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  946. en:birnbaum's syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:birnbaum's syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  947. en:breast atrophy --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:breast atrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  948. en:cap myopathy --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:cap myopathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  949. en:cerebellar ataxia ectodermal dysplasia --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:cerebellar ataxia ectodermal dysplasia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  950. en:cerebral hemorrhage with amyloidosis, hereditary, dutch type --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  951. en:chemically induced --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:chemically induced | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  952. en:circumscribed hypermelanosis --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:circumscribed hypermelanosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  953. en:congenital cataracts, facial dysmorphism, and neuropathy --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:congenital cataracts, facial dysmorphism, and neuropathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  954. en:congenital dyserythropoietic anemia, type iii --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:congenital dyserythropoietic anemia, type iii | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  955. en:congenital nephrogenic diabetes insipidus --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:congenital nephrogenic diabetes insipidus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  956. en:congenital/hereditary lentiginosis --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:congenital/hereditary lentiginosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  957. en:cutaneous photosensitivity and lethal colitis syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:cutaneous photosensitivity and lethal colitis syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  958. en:de toni-debre-fanconi syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:de toni-debre-fanconi syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  959. en:depigmentation --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:depigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  960. en:developmental anomaly --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:developmental anomaly | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  961. en:digestive system adenoma --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:digestive system adenoma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  962. en:disseminated superficial porokeratosis --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:disseminated superficial porokeratosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  963. en:dominant autosomal hereditary disorder, complete penetrance --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:dominant autosomal hereditary disorder, complete penetrance | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  964. en:familial arthrogryposis-cholestatic hepatorenal syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:familial arthrogryposis-cholestatic hepatorenal syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  965. en:hashimoto-pritzker syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:hashimoto-pritzker syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  966. en:hereditary papillary renal cell carcinoma --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:hereditary papillary renal cell carcinoma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  967. en:hyperbilirubinaemia --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:hyperbilirubinaemia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  968. en:hyperinsulinism due to deficiency of glucokinase --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:hyperinsulinism due to deficiency of glucokinase | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  969. en:hypomagnesemia 1, intestinal --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:hypomagnesemia 1, intestinal | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  970. en:intestinal angioma --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:intestinal angioma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  971. en:jackson-weiss syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:jackson-weiss syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  972. en:large intestine atresia --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:large intestine atresia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  973. en:leigh disease --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:leigh disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  974. en:lowry yong syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:lowry yong syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  975. en:may-hegglin anomaly --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:may-hegglin anomaly | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  976. en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  977. en:mixed hypo- and hyperpigmentation of the skin --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:mixed hypo- and hyperpigmentation of the skin | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  978. en:moloney syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:moloney syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  979. en:mosaic variegated aneuploidy --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:mosaic variegated aneuploidy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  980. en:multiple self healing epithelioma of ferguson-smith --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:multiple self healing epithelioma of ferguson-smith | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  981. en:neuropathy, hereditary thermosensitive --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:neuropathy, hereditary thermosensitive | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  982. en:oculocerebral hypopigmentation syndrome type preus --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:oculocerebral hypopigmentation syndrome type preus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  983. en:oculodental syndrome rutherfurd syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:oculodental syndrome rutherfurd syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  984. en:osteous demineralization --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:osteous demineralization | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  985. en:ovarian sex cord-stromal tumor --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:ovarian sex cord-stromal tumor | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  986. en:pseudoatrophoderma colli --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:pseudoatrophoderma colli | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  987. en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  988. en:reardon hall slaney syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:reardon hall slaney syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  989. en:retroperitoneal cyst --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:retroperitoneal cyst | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  990. en:roentgenographic --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:roentgenographic | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  991. en:rud syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:rud syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  992. en:schinzel-giedion midface-retraction syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:schinzel-giedion midface-retraction syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  993. en:sebastian syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:sebastian syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  994. en:skin discoloration --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:skin discoloration | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  995. en:stk11, 1-bp del, 890g --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:stk11, 1-bp del, 890g | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  996. en:stk11, tyr246ter --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:stk11, tyr246ter | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  997. en:syndactyly, type iii --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:syndactyly, type iii | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  998. en:verruciform xanthoma of oral mucous membrane --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:verruciform xanthoma of oral mucous membrane | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  999. en:vitiligo --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:vitiligo | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  1000. en:wells jankovic syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:wells jankovic syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  1001. en:x-linked intellectual disability with ataxia and apraxia syndrome --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:x-linked intellectual disability with ataxia and apraxia syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  1002. en:xanthoma tendinosum --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=en:xanthoma tendinosum | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  1003. ethnologique --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=ethnologique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  1004. syndrome d'alagille --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=syndrome d'alagille | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  1005. syndrome de gorlin --- r_associated #0: 27 --> en:peutz-jeghers syndrome
    n1=syndrome de gorlin | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27
  1006. Recklinghausen (maladie de von) --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=Recklinghausen (maladie de von) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1007. atrophie optique, cataracte, et troubles neurologiques --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=atrophie optique, cataracte, et troubles neurologiques | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1008. en:Peutz-Jeghers's syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:Peutz-Jeghers's syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1009. en:advanced sleep-phase syndrome, familial --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:advanced sleep-phase syndrome, familial | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1010. en:alpha-1 antitrypsin deficiency --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:alpha-1 antitrypsin deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1011. en:aplasia of lacrimal and salivary glands --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:aplasia of lacrimal and salivary glands | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1012. en:autosomal dominant charcot-marie-tooth disease type 2a1 --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant charcot-marie-tooth disease type 2a1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1013. en:autosomal dominant hyperinsulinism due to kir6.2 deficiency --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1014. en:autosomal dominant hyperinsulinism due to sur1 deficiency --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:autosomal dominant hyperinsulinism due to sur1 deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1015. en:avascular necrosis of femoral head --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:avascular necrosis of femoral head | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1016. en:bilateral multiple fibroadenoma of breast --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:bilateral multiple fibroadenoma of breast | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1017. en:bilateral pheochromocytoma and islet cell adenoma of the pancreas --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1018. en:brachyolmia type 3 --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:brachyolmia type 3 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1019. en:cardiac anomaly and heterotaxy syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:cardiac anomaly and heterotaxy syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1020. en:cataract glaucoma syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:cataract glaucoma syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1021. en:cerebellar ataxia, cayman type --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:cerebellar ataxia, cayman type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1022. en:cervical carcinoma --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:cervical carcinoma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1023. en:char syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:char syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1024. en:complex regional pain syndrome i --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:complex regional pain syndrome i | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1025. en:congenital enterocyte heparan sulfate deficiency --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:congenital enterocyte heparan sulfate deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1026. en:congenital malformation of upper alimentary tract --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:congenital malformation of upper alimentary tract | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1027. en:congenital sucrase-isomaltase deficiency --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:congenital sucrase-isomaltase deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1028. en:degenerative disorder of head --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:degenerative disorder of head | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1029. en:dominant autosomal hereditary disorder, incomplete penetrance --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:dominant autosomal hereditary disorder, incomplete penetrance | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1030. en:dystrophic cardiomyopathy --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:dystrophic cardiomyopathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1031. en:epidermolysis bullosa simplex with pyloric atresia --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:epidermolysis bullosa simplex with pyloric atresia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1032. en:etiology aspects --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:etiology aspects | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1033. en:extraosseous calcification --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:extraosseous calcification | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1034. en:familial acantholysis --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:familial acantholysis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1035. en:familial digital arthropathy and brachydactyly syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:familial digital arthropathy and brachydactyly syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1036. en:familial multiple tumor syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:familial multiple tumor syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1037. en:folinic acid responsive seizure syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:folinic acid responsive seizure syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1038. en:glycogen storage disease, hepatic form --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:glycogen storage disease, hepatic form | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1039. en:gracile bone dysplasia --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:gracile bone dysplasia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1040. en:hereditary palmoplantar keratoderma gamborg nielsen type --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:hereditary palmoplantar keratoderma gamborg nielsen type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1041. en:hydrocephalus with cerebellar agenesis --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:hydrocephalus with cerebellar agenesis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1042. en:hyperinsulinism due to hnf1a deficiency --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:hyperinsulinism due to hnf1a deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1043. en:hyperinsulinism due to hnf4a deficiency --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:hyperinsulinism due to hnf4a deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1044. en:hypermelanosis following phototherapy for neonatal jaundice --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:hypermelanosis following phototherapy for neonatal jaundice | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1045. en:hypertrichosis and acromegaloid facial appearance syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:hypertrichosis and acromegaloid facial appearance syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1046. en:hypoplastic tibia and postaxial polydactyly syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:hypoplastic tibia and postaxial polydactyly syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1047. en:hypothalamic hamartoblastoma --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:hypothalamic hamartoblastoma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1048. en:ichthyosis congenita with biliary atresia --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:ichthyosis congenita with biliary atresia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1049. en:intestinal disorders congenital --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:intestinal disorders congenital | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1050. en:isaacs syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:isaacs syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1051. en:juvenile osteochondrosis of foot, nos --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:juvenile osteochondrosis of foot, nos | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1052. en:kbg syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:kbg syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1053. en:knobloch syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:knobloch syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1054. en:macdermot winter syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:macdermot winter syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1055. en:maternally inherited mitochondrial dystonia --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:maternally inherited mitochondrial dystonia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1056. en:megalencephaly cutis marmorata telangiectatica congenita --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:megalencephaly cutis marmorata telangiectatica congenita | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1057. en:melanoderma (disorder) --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:melanoderma (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1058. en:melanosis --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:melanosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1059. en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1060. en:mutyh-associated polyposis --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:mutyh-associated polyposis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1061. en:myxoid transformation of cardiac valve --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:myxoid transformation of cardiac valve | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1062. en:nemaline myopathy 3 --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:nemaline myopathy 3 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1063. en:neuronal ceroid lipofuscinosis type 3 --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:neuronal ceroid lipofuscinosis type 3 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1064. en:nevus of ota --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:nevus of ota | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1065. en:noonan syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:noonan syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1066. en:ophthalmoplegia --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:ophthalmoplegia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1067. en:osteolysis --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:osteolysis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1068. en:other congenital malformations of digestive system --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:other congenital malformations of digestive system | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1069. en:peripheral resistance to thyroid hormone --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:peripheral resistance to thyroid hormone | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1070. en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1071. en:port wine stain --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:port wine stain | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1072. en:proctatresia --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:proctatresia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1073. en:pseudohypoaldosteronism, type 1, dominant form --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:pseudohypoaldosteronism, type 1, dominant form | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1074. en:psychology qualifier --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:psychology qualifier | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1075. en:skin hyperpigmentation --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:skin hyperpigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1076. en:solar lentigo --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:solar lentigo | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1077. en:spinocerebellar ataxia type 2 --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:spinocerebellar ataxia type 2 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1078. en:spinocerebellar ataxia type 4 --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:spinocerebellar ataxia type 4 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1079. en:steatocystoma multiplex with natal tooth syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:steatocystoma multiplex with natal tooth syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1080. en:syndromic orbital border hypoplasia --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:syndromic orbital border hypoplasia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1081. en:tmem70 related mitochondrial encephalo-cardio-myopathy --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:tmem70 related mitochondrial encephalo-cardio-myopathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1082. en:treacher collins syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:treacher collins syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1083. en:tungland bellman syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:tungland bellman syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1084. en:vitello-intestinal duct remnant --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:vitello-intestinal duct remnant | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1085. en:vitreoretinochoroidopathy (disorder) --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:vitreoretinochoroidopathy (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1086. en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1087. en:wnt4 mullerian aplasia and ovarian dysfunction --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:wnt4 mullerian aplasia and ovarian dysfunction | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1088. en:x-linked agammaglobulinemia --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:x-linked agammaglobulinemia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1089. en:zinc-deficiency type --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=en:zinc-deficiency type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1090. hypopituitarisme --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=hypopituitarisme | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1091. ostéolyse --- r_associated #0: 26 --> en:peutz-jeghers syndrome
    n1=ostéolyse | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26
  1092. Lynch (syndrome de) --- r_associated #0: 25 --> en:peutz-jeghers syndrome
    n1=Lynch (syndrome de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=25
  1093. albinisme avec pigmentation minime --- r_associated #0: 25 --> en:peutz-jeghers syndrome
    n1=albinisme avec pigmentation minime | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=25
  1094. cancer du sein --- r_associated #0: 25 --> en:peutz-jeghers syndrome
    n1=cancer du sein | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=25
  1095. en:Alagille's syndrome --- r_associated #0: 25 --> en:peutz-jeghers syndrome
    n1=en:Alagille's syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=25
  1096. en:Osler-Rendu-Weber disease --- r_associated #0: 25 --> en:peutz-jeghers syndrome
    n1=en:Osler-Rendu-Weber disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=25
  1097. en:Osler-Rendu-Weber's disease --- r_associated #0: 25 --> en:peutz-jeghers syndrome
    n1=en:Osler-Rendu-Weber's disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=25
  1098. en:intestinal polyps --- r_associated #0: 25 --> en:peutz-jeghers syndrome
    n1=en:intestinal polyps | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=25
  1099. en:nursing therapy --- r_associated #0: 25 --> en:peutz-jeghers syndrome
    n1=en:nursing therapy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=25
  1100. en:spastic paraplegia --- r_associated #0: 25 --> en:peutz-jeghers syndrome
    n1=en:spastic paraplegia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=25
  1101. en:type a 14 --- r_associated #0: 25 --> en:peutz-jeghers syndrome
    n1=en:type a 14 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=25
  1102. malformation --- r_associated #0: 25 --> en:peutz-jeghers syndrome
    n1=malformation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=25
  1103. phacomatose --- r_associated #0: 25 --> en:peutz-jeghers syndrome
    n1=phacomatose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=25
  1104. sclérodermie tubéreuse de bourneville --- r_associated #0: 25 --> en:peutz-jeghers syndrome
    n1=sclérodermie tubéreuse de bourneville | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=25
  1105. albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception --- r_associated #0: 24 --> en:peutz-jeghers syndrome
    n1=albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=24
  1106. anus ectopique --- r_associated #0: 24 --> en:peutz-jeghers syndrome
    n1=anus ectopique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=24
  1107. atrophie optique infantile héréditaire compliquée de Behr --- r_associated #0: 24 --> en:peutz-jeghers syndrome
    n1=atrophie optique infantile héréditaire compliquée de Behr | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=24
  1108. corne cutanée de la paupière --- r_associated #0: 24 --> en:peutz-jeghers syndrome
    n1=corne cutanée de la paupière | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=24
  1109. en:cutaneous atrophy --- r_associated #0: 24 --> en:peutz-jeghers syndrome
    n1=en:cutaneous atrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=24
  1110. en:intra-abdominal hemangioma --- r_associated #0: 24 --> en:peutz-jeghers syndrome
    n1=en:intra-abdominal hemangioma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=24
  1111. maladie de dubin-johnson --- r_associated #0: 24 --> en:peutz-jeghers syndrome
    n1=maladie de dubin-johnson | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=24
  1112. xanthique (lithiase) --- r_associated #0: 24 --> en:peutz-jeghers syndrome
    n1=xanthique (lithiase) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=24
  1113. Marfan (maladie de) --- r_associated #0: 23 --> en:peutz-jeghers syndrome
    n1=Marfan (maladie de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=23
  1114. artériosclérose sévère juvénile de Kaitila --- r_associated #0: 23 --> en:peutz-jeghers syndrome
    n1=artériosclérose sévère juvénile de Kaitila | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=23
  1115. atrophie optique infantile avec chorée et paraplégie spastique --- r_associated #0: 23 --> en:peutz-jeghers syndrome
    n1=atrophie optique infantile avec chorée et paraplégie spastique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=23
  1116. atrophie optique, surdité, ophtalmoplégie et myopathie --- r_associated #0: 23 --> en:peutz-jeghers syndrome
    n1=atrophie optique, surdité, ophtalmoplégie et myopathie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=23
  1117. en:Gorlin syndrome --- r_associated #0: 23 --> en:peutz-jeghers syndrome
    n1=en:Gorlin syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=23
  1118. en:anal imperforation --- r_associated #0: 23 --> en:peutz-jeghers syndrome
    n1=en:anal imperforation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=23
  1119. en:congenital anomaly of gastrointestinal tract --- r_associated #0: 23 --> en:peutz-jeghers syndrome
    n1=en:congenital anomaly of gastrointestinal tract | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=23
  1120. en:congenital intestinal malformation --- r_associated #0: 23 --> en:peutz-jeghers syndrome
    n1=en:congenital intestinal malformation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=23
  1121. en:generalized hyperpigmentation --- r_associated #0: 23 --> en:peutz-jeghers syndrome
    n1=en:generalized hyperpigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=23
  1122. en:idiopathic lenticular mucocutaneous pigmentation --- r_associated #0: 23 --> en:peutz-jeghers syndrome
    n1=en:idiopathic lenticular mucocutaneous pigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=23
  1123. en:yellow nail --- r_associated #0: 23 --> en:peutz-jeghers syndrome
    n1=en:yellow nail | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=23
  1124. tylose --- r_associated #0: 23 --> en:peutz-jeghers syndrome
    n1=tylose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=23
  1125. en:adenomatosis coli --- r_associated #0: 22 --> en:peutz-jeghers syndrome
    n1=en:adenomatosis coli | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=22
  1126. en:and myopathy --- r_associated #0: 22 --> en:peutz-jeghers syndrome
    n1=en:and myopathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=22
  1127. en:congenital anomaly of stomach --- r_associated #0: 22 --> en:peutz-jeghers syndrome
    n1=en:congenital anomaly of stomach | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=22
  1128. en:lentigo simplex --- r_associated #0: 22 --> en:peutz-jeghers syndrome
    n1=en:lentigo simplex | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=22
  1129. en:marfan's syndrome --- r_associated #0: 22 --> en:peutz-jeghers syndrome
    n1=en:marfan's syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=22
  1130. en:tofus --- r_associated #0: 22 --> en:peutz-jeghers syndrome
    n1=en:tofus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=22
  1131. en:toxic melanoderma of Hoffmann-Habermann --- r_associated #0: 22 --> en:peutz-jeghers syndrome
    n1=en:toxic melanoderma of Hoffmann-Habermann | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=22
  1132. McCune-Albright (syndrome de) --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=McCune-Albright (syndrome de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1133. adénomatose recto-colique familiale --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=adénomatose recto-colique familiale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1134. angiome plan --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=angiome plan | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1135. argyrie --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=argyrie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1136. byssinose --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=byssinose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1137. cataracte liée au sexe avec dent de Hutchinson --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=cataracte liée au sexe avec dent de Hutchinson | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1138. en:Bessel-Hagen's disease --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=en:Bessel-Hagen's disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1139. en:basal cell nævus --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=en:basal cell nævus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1140. en:congenital melanosis --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=en:congenital melanosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1141. en:dolichocolon --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=en:dolichocolon | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1142. en:hereditary motor and sensory neuropathy type I --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=en:hereditary motor and sensory neuropathy type I | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1143. en:hypopituitarism --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=en:hypopituitarism | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1144. en:mental retardation --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=en:mental retardation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1145. en:onychoosteodysostosis --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=en:onychoosteodysostosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1146. en:poikiloderma of Civatte --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=en:poikiloderma of Civatte | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1147. en:small intestinal polyposis --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=en:small intestinal polyposis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1148. en:venosclerosis --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=en:venosclerosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1149. nystagmus héréditaire vertical --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=nystagmus héréditaire vertical | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1150. syndrome des ongles jaunes --- r_associated #0: 21 --> en:peutz-jeghers syndrome
    n1=syndrome des ongles jaunes | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=21
  1151. Atrésie de l'oesophage --- r_associated #0: 20 --> en:peutz-jeghers syndrome
    n1=Atrésie de l'oesophage | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=20
  1152. Dépigmentation --- r_associated #0: 20 --> en:peutz-jeghers syndrome
    n1=Dépigmentation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=20
  1153. Malformation --- r_associated #0: 20 --> en:peutz-jeghers syndrome
    n1=Malformation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=20
  1154. Ostéolyse --- r_associated #0: 20 --> en:peutz-jeghers syndrome
    n1=Ostéolyse | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=20
  1155. Rhabdomyolyse --- r_associated #0: 20 --> en:peutz-jeghers syndrome
    n1=Rhabdomyolyse | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=20
  1156. en:Carney complex --- r_associated #0: 20 --> en:peutz-jeghers syndrome
    n1=en:Carney complex | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=20
  1157. en:LEOPARD syndrome --- r_associated #0: 20 --> en:peutz-jeghers syndrome
    n1=en:LEOPARD syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=20
  1158. vitiligo --- r_associated #0: 20 --> en:peutz-jeghers syndrome
    n1=vitiligo | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=20
  1159. syndrome de Warburg --- r_associated #0: 16 --> en:peutz-jeghers syndrome
    n1=syndrome de Warburg | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=16
  1160. Albert (position d') --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Albert (position d') | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1161. Atrésie de l'œsophage --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Atrésie de l'œsophage | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1162. BWAV --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=BWAV | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1163. Cancer du sein --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Cancer du sein | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1164. Chernosky (hyperpigmentation familiale progressive de) --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Chernosky (hyperpigmentation familiale progressive de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1165. Enzymologie --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Enzymologie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1166. Giessen (test de) --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Giessen (test de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1167. Kyste ovarien --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Kyste ovarien | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1168. Maladie de Marfan --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Maladie de Marfan | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1169. Malformation congénitale --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Malformation congénitale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1170. Microbiologique --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Microbiologique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1171. Ostéopénie --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Ostéopénie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1172. Parasitologie --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Parasitologie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1173. Peutz-Jeghers (syndrome de) --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Peutz-Jeghers (syndrome de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1174. Syndrome de Lynch --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Syndrome de Lynch | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1175. Syndrome de Walker-Warburg --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Syndrome de Walker-Warburg | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1176. Tumeurs du pancréas --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=Tumeurs du pancréas | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1177. diverticulaire (maladie) --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=diverticulaire (maladie) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1178. démence (sémiologie) --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=démence (sémiologie) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1179. en:phantom bone --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=en:phantom bone | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1180. en:tylose --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=en:tylose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1181. malentendant (enfant) --- r_associated #0: 15 --> en:peutz-jeghers syndrome
    n1=malentendant (enfant) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=15
  1182. insomnie familiale fatale --- r_associated #0: 11 --> en:peutz-jeghers syndrome
    n1=insomnie familiale fatale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=11
  1183. marque de naissance --- r_associated #0: 11 --> en:peutz-jeghers syndrome
    n1=marque de naissance | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=11
  1184. urticaire-surdité-amylose rénale --- r_associated #0: 11 --> en:peutz-jeghers syndrome
    n1=urticaire-surdité-amylose rénale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=11
  1185. Albinisme --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Albinisme | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1186. Argyll-Robertson (signe d') --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Argyll-Robertson (signe d') | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1187. Artériosclérose --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Artériosclérose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1188. Atrophie --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Atrophie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1189. Bessel-Hagen (maladie de) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Bessel-Hagen (maladie de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1190. Byler (maladie de) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Byler (maladie de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1191. CONGENITAL --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=CONGENITAL | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1192. CONGÉNITALE --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=CONGÉNITALE | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1193. CX3CL1 --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=CX3CL1 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1194. Congenital --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Congenital | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1195. Dubin-Johnson (syndrome de) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Dubin-Johnson (syndrome de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1196. Dystrophy --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Dystrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1197. Démyélinisation --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Démyélinisation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1198. Gorlin (syndrome de) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Gorlin (syndrome de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1199. Haltia-Santavuori (maladie de) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Haltia-Santavuori (maladie de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1200. Insler et Bernstein (score cervical d') --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Insler et Bernstein (score cervical d') | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1201. Lung --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Lung | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1202. MELAS (syndrome) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=MELAS (syndrome) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1203. MIGP (orientation) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=MIGP (orientation) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1204. Neurofibromatose --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Neurofibromatose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1205. Ostéomalacie --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Ostéomalacie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1206. POEMS (syndrome) pour --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=POEMS (syndrome) pour | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1207. Paraquat ® (intoxication par le) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Paraquat ® (intoxication par le) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1208. Peutz-Touraine-Jeghers (syndrome de) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Peutz-Touraine-Jeghers (syndrome de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1209. Syndrome de Sotos --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Syndrome de Sotos | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1210. Syndrome myéloprolifératif (classification et pronostic) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Syndrome myéloprolifératif (classification et pronostic) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1211. Teissier (spatule de) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Teissier (spatule de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1212. Treft-Sanborn-Carey (syndrome de) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Treft-Sanborn-Carey (syndrome de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1213. Tylosis --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Tylosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1214. Yellen-Gomco (clamp de) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=Yellen-Gomco (clamp de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1215. absence d'empreintes digitales avec syndrome de milia congénital --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=absence d'empreintes digitales avec syndrome de milia congénital | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1216. angl. HNPCC --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=angl. HNPCC | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1217. arriération --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=arriération | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1218. atrophie optique, surdité neurogène, amyotrophie distale neurogénique --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=atrophie optique, surdité neurogène, amyotrophie distale neurogénique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1219. bilieuse hémoglobinurique (fièvre) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=bilieuse hémoglobinurique (fièvre) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1220. débilité mentale --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=débilité mentale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1221. dépendance environnementale (syndrome de) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=dépendance environnementale (syndrome de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1222. en:5q microdeletion --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:5q microdeletion | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1223. en:Albert's position --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:Albert's position | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1224. en:Kjer type optic atrophy --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:Kjer type optic atrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1225. en:Kjer's type --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:Kjer's type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1226. en:Recklinghausen's disease --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:Recklinghausen's disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1227. en:Schmorl's jaundice --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:Schmorl's jaundice | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1228. en:Sotos's syndrome --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:Sotos's syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1229. en:and dementia --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:and dementia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1230. en:and microgenitalism --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:and microgenitalism | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1231. en:and postaxil polydactylie --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:and postaxil polydactylie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1232. en:atresia ani --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:atresia ani | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1233. en:atypical nevus syndrome --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:atypical nevus syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1234. en:bilirubin encephalopathy --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:bilirubin encephalopathy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1235. en:bilirubinemia --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:bilirubinemia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1236. en:breastcancer --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:breastcancer | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1237. en:cacomorphosis --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:cacomorphosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1238. en:cancer of the breast --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:cancer of the breast | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1239. en:capillary haemangiomata --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:capillary haemangiomata | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1240. en:capillary nevus --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:capillary nevus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1241. en:carcinoma of the breast --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:carcinoma of the breast | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1242. en:cataract --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:cataract | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1243. en:contractural arachnodactyly --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:contractural arachnodactyly | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1244. en:cotton-mill fever --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:cotton-mill fever | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1245. en:creeps --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:creeps | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1246. en:diverticular disease --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:diverticular disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1247. en:dysplastic nevus syndrome hereditary --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:dysplastic nevus syndrome hereditary | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1248. en:erythroblastosis fetalis --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:erythroblastosis fetalis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1249. en:ethnological --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:ethnological | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1250. en:hemangioma simplex --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:hemangioma simplex | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1251. en:hypoacousic child --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:hypoacousic child | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1252. en:infantile finnish type --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:infantile finnish type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1253. en:iron deficiency anemia --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:iron deficiency anemia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1254. en:late optic atrophy --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:late optic atrophy | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1255. en:mastocarcinoma --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:mastocarcinoma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1256. en:minimal pigment type --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:minimal pigment type | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1257. en:nuclear icterus --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:nuclear icterus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1258. en:nuclear jaundice --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:nuclear jaundice | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1259. en:nystagmuses --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:nystagmuses | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1260. en:nystaxis --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:nystaxis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1261. en:radiographic --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:radiographic | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1262. en:talantropia --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:talantropia | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1263. en:telangiectoma --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:telangiectoma | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1264. en:type 2B or 3 --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:type 2B or 3 | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1265. en:type I --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:type I | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1266. en:type VI --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:type VI | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1267. en:von recklinghausen's disease --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:von recklinghausen's disease | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1268. en:with growth retardation --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:with growth retardation | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1269. en:with tapetal-like sheen --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:with tapetal-like sheen | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1270. en:xanthine lithiasis --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:xanthine lithiasis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1271. en:xanthonychia syndrome --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:xanthonychia syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1272. en:xanthonychie --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=en:xanthonychie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1273. exostose du conduit auditif externe --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=exostose du conduit auditif externe | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1274. exostose ostéocartilagineuse --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=exostose ostéocartilagineuse | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1275. exostose sous-unguéale --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=exostose sous-unguéale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1276. exostosectomie --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=exostosectomie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1277. goniome --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=goniome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1278. goniomètre --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=goniomètre | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1279. gonion --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=gonion | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1280. gonioscopie --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=gonioscopie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1281. goniosynéchies --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=goniosynéchies | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1282. goniotomie endoscopique --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=goniotomie endoscopique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1283. gonochorisme --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=gonochorisme | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1284. gonococcie --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=gonococcie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1285. gonocoque --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=gonocoque | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1286. gonocyte --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=gonocyte | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1287. gonocytome --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=gonocytome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1288. gonométrie --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=gonométrie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1289. gonorrhée --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=gonorrhée | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1290. gonosome --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=gonosome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1291. gonosomique --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=gonosomique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1292. hypohypophysie --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=hypohypophysie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1293. hypostimulinie --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=hypostimulinie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1294. impédance acoustique (symb. Z) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=impédance acoustique (symb. Z) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1295. lentigo simplex --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=lentigo simplex | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1296. melanosis --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=melanosis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1297. neuropathie sensitivomotrice héréditaire forme I --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=neuropathie sensitivomotrice héréditaire forme I | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1298. nystagmus myoclonies --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=nystagmus myoclonies | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1299. néoplasie endocrinienne multiple de type 2A (MEN 2A) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=néoplasie endocrinienne multiple de type 2A (MEN 2A) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1300. paraplégie spastique dans la syphilis congénitale --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=paraplégie spastique dans la syphilis congénitale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1301. paraplégie spastique familiale --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=paraplégie spastique familiale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1302. polyphosphorique (acide) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=polyphosphorique (acide) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1303. porphyrie --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=porphyrie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1304. poïkilodermie réticulée pigmentaire du visage et du cou de Civatte --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=poïkilodermie réticulée pigmentaire du visage et du cou de Civatte | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1305. reclassement professionnel --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=reclassement professionnel | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1306. rétinite pigmentaire, surdité, retard mental, et hypogonadisme --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=rétinite pigmentaire, surdité, retard mental, et hypogonadisme | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1307. souche de référence --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=souche de référence | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1308. souche transduite --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=souche transduite | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1309. surdité --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=surdité | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1310. syndrome cataracte-ataxie-surdité et retard mental --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=syndrome cataracte-ataxie-surdité et retard mental | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1311. syndrome d'Apert --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=syndrome d'Apert | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1312. syndrome d'hyperparathyroïdie et tumeur de la mâchoire --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=syndrome d'hyperparathyroïdie et tumeur de la mâchoire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1313. syndrome de Feingold --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=syndrome de Feingold | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1314. syndrome de Mohr-Tranebjaerg --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=syndrome de Mohr-Tranebjaerg | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1315. syndrome de Pitt-Hopkins --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=syndrome de Pitt-Hopkins | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1316. syndrome de prédisposition aux tumeurs rhabdoïdes --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=syndrome de prédisposition aux tumeurs rhabdoïdes | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1317. syndrome de warburg --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=syndrome de warburg | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1318. tache de naissance --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=tache de naissance | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1319. tumeur de Wilms du rein --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=tumeur de Wilms du rein | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1320. tumeur des cordons sexuels et du stroma ovarien --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=tumeur des cordons sexuels et du stroma ovarien | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1321. tumeur germinale testiculaire maligne --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=tumeur germinale testiculaire maligne | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1322. ty (élément) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=ty (élément) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1323. von Recklinghausen (maladie de) --- r_associated #0: 10 --> en:peutz-jeghers syndrome
    n1=von Recklinghausen (maladie de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
  1324. diverticule de l'iléon --- r_associated #0: 6 --> en:peutz-jeghers syndrome
    n1=diverticule de l'iléon | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=6
  1325. Alagille (syndrome d') --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=Alagille (syndrome d') | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1326. Anémie ferriprive --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=Anémie ferriprive | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1327. Hypopituitarisme --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=Hypopituitarisme | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1328. Nyssen-van Bogaert (syndrome de) --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=Nyssen-van Bogaert (syndrome de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1329. Onsager (relation d') --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=Onsager (relation d') | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1330. Stokvis-Talma (syndrome de) --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=Stokvis-Talma (syndrome de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1331. albinisme avec immunodéficience et troubles hématologiques --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=albinisme avec immunodéficience et troubles hématologiques | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1332. albinisme avec surdité --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=albinisme avec surdité | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1333. diverticule caliciel --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=diverticule caliciel | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1334. diverticule de l'ampoule du conduit déférent --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=diverticule de l'ampoule du conduit déférent | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1335. diverticule de l'oesophage --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=diverticule de l'oesophage | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1336. diverticule de la trompe de Fallope --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=diverticule de la trompe de Fallope | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1337. diverticule de la voie excrétrice urinaire --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=diverticule de la voie excrétrice urinaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1338. démence d'Alzheimer --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=démence d'Alzheimer | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1339. kératohyaline (grains de) --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=kératohyaline (grains de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1340. lynestrénol --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=lynestrénol | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1341. lyo-enzyme --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=lyo-enzyme | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1342. lyoglycogène --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=lyoglycogène | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1343. malf ormation dysraphique --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=malf ormation dysraphique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1344. malformation kystique adénomatoïde du poumon --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=malformation kystique adénomatoïde du poumon | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1345. malformation luxante de la hanche --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=malformation luxante de la hanche | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1346. malformation mamelonnaire --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=malformation mamelonnaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1347. malformation mammaire --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=malformation mammaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1348. malformation ombilicale --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=malformation ombilicale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1349. malformation utérine --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=malformation utérine | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1350. malformation vaginale --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=malformation vaginale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1351. malformation vasculaire cérébrale du nourrisson --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=malformation vasculaire cérébrale du nourrisson | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1352. malformations de la charnière occipitocervicale --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=malformations de la charnière occipitocervicale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1353. mcd --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=mcd | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1354. mélanisation (unité épidermique de) --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=mélanisation (unité épidermique de) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1355. nystagmus (zone de moindre) --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=nystagmus (zone de moindre) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1356. nævique irien (syndrome) --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=nævique irien (syndrome) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1357. nævus dysplasique héréditaire --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=nævus dysplasique héréditaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1358. nævus eccrine --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=nævus eccrine | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1359. nævus elasticus --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=nævus elasticus | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1360. nævus élastique en tumeurs disséminées --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=nævus élastique en tumeurs disséminées | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1361. nævus épidermique --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=nævus épidermique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1362. onychodysplasie --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=onychodysplasie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1363. onychogryphose --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=onychogryphose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1364. onycholyse --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=onycholyse | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1365. onycholyse candidosique --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=onycholyse candidosique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1366. onycholyse semi-lunaire partielle --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=onycholyse semi-lunaire partielle | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1367. onychomadèse --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=onychomadèse | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1368. onychomatricome --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=onychomatricome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1369. pancréas aberrant --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=pancréas aberrant | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1370. pancréas accessoire --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=pancréas accessoire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1371. pancréas annulaire --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=pancréas annulaire | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1372. pancréas artificiel --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=pancréas artificiel | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1373. pancréas de Willis --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=pancréas de Willis | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1374. pancréas de Winslow --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=pancréas de Winslow | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1375. pancréas divisum --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=pancréas divisum | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1376. pancréastatine --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=pancréastatine | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1377. paraphimosis (réduction d'un) --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=paraphimosis (réduction d'un) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1378. retardation mentale --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=retardation mentale | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1379. syndrome tumeur de Wilms-aniridie-anomalies génito-urinaires-retard mental --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=syndrome tumeur de Wilms-aniridie-anomalies génito-urinaires-retard mental | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1380. syndrome tumeur de Wilms-aniridie-anomalies génito-urinaires-retard mental-obésité --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=syndrome tumeur de Wilms-aniridie-anomalies génito-urinaires-retard mental-obésité | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1381. xanthoastrocytome pléomorphe --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=xanthoastrocytome pléomorphe | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1382. xanthochromie --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=xanthochromie | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1383. xanthochromie caroténique --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=xanthochromie caroténique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1384. xanthoerythrodermia perstans --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=xanthoerythrodermia perstans | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1385. xanthogranulome juvénile --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=xanthogranulome juvénile | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1386. xanthogranulome nécrobiotique --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=xanthogranulome nécrobiotique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1387. xanthogranulome palpébral --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=xanthogranulome palpébral | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1388. xanthohistiocytome --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=xanthohistiocytome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1389. xanthoma disseminatum --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=xanthoma disseminatum | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
  1390. xanthomatose --- r_associated #0: 5 --> en:peutz-jeghers syndrome
    n1=xanthomatose | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=5
Le service Rézo permet d'énumérer les relations existant pour un terme. Ce service est interrogeable par programme.
Projet JeuxDeMots - url: http://www.jeuxdemots.org
contact: mathieu.lafourcade@lirmm.fr