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'en:major congenital anomaly'
(id=6890938 ; fe=en:major congenital anomaly ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=24934 creation date=2017-06-25 touchdate=2025-07-13 21:22:51.000)
≈ 285 relations sortantes

  1. en:major congenital anomaly -- r_associated #0: 42 / 1 -> en:congenital morphologic anomaly
    n1=en:major congenital anomaly | n2=en:congenital morphologic anomaly | rel=r_associated | relid=0 | w=42
  2. en:major congenital anomaly -- r_associated #0: 41 / 0.976 -> en:gastroschisis
    n1=en:major congenital anomaly | n2=en:gastroschisis | rel=r_associated | relid=0 | w=41
  3. en:major congenital anomaly -- r_associated #0: 39 / 0.929 -> en:congenital disruption
    n1=en:major congenital anomaly | n2=en:congenital disruption | rel=r_associated | relid=0 | w=39
  4. en:major congenital anomaly -- r_associated #0: 38 / 0.905 -> en:cryptophthalmia
    n1=en:major congenital anomaly | n2=en:cryptophthalmia | rel=r_associated | relid=0 | w=38
  5. en:major congenital anomaly -- r_associated #0: 35 / 0.833 -> en:anomaly congenital special senses
    n1=en:major congenital anomaly | n2=en:anomaly congenital special senses | rel=r_associated | relid=0 | w=35
  6. en:major congenital anomaly -- r_associated #0: 35 / 0.833 -> en:cleft jaw
    n1=en:major congenital anomaly | n2=en:cleft jaw | rel=r_associated | relid=0 | w=35
  7. en:major congenital anomaly -- r_associated #0: 35 / 0.833 -> en:congenital eye disorder
    n1=en:major congenital anomaly | n2=en:congenital eye disorder | rel=r_associated | relid=0 | w=35
  8. en:major congenital anomaly -- r_associated #0: 35 / 0.833 -> en:congenital systemic disorder
    n1=en:major congenital anomaly | n2=en:congenital systemic disorder | rel=r_associated | relid=0 | w=35
  9. en:major congenital anomaly -- r_associated #0: 35 / 0.833 -> en:connatal disorder
    n1=en:major congenital anomaly | n2=en:connatal disorder | rel=r_associated | relid=0 | w=35
  10. en:major congenital anomaly -- r_associated #0: 35 / 0.833 -> en:ectopia cordis
    n1=en:major congenital anomaly | n2=en:ectopia cordis | rel=r_associated | relid=0 | w=35
  11. en:major congenital anomaly -- r_associated #0: 35 / 0.833 -> en:lymphatic abnormalities
    n1=en:major congenital anomaly | n2=en:lymphatic abnormalities | rel=r_associated | relid=0 | w=35
  12. en:major congenital anomaly -- r_associated #0: 35 / 0.833 -> en:spina bifida
    n1=en:major congenital anomaly | n2=en:spina bifida | rel=r_associated | relid=0 | w=35
  13. en:major congenital anomaly -- r_associated #0: 35 / 0.833 -> en:ventricular septal defect
    n1=en:major congenital anomaly | n2=en:ventricular septal defect | rel=r_associated | relid=0 | w=35
  14. en:major congenital anomaly -- r_associated #0: 34 / 0.81 -> en:abnormalities, drug-induced
    n1=en:major congenital anomaly | n2=en:abnormalities, drug-induced | rel=r_associated | relid=0 | w=34
  15. en:major congenital anomaly -- r_associated #0: 34 / 0.81 -> en:amastia
    n1=en:major congenital anomaly | n2=en:amastia | rel=r_associated | relid=0 | w=34
  16. en:major congenital anomaly -- r_associated #0: 34 / 0.81 -> en:branchial cleft remnant
    n1=en:major congenital anomaly | n2=en:branchial cleft remnant | rel=r_associated | relid=0 | w=34
  17. en:major congenital anomaly -- r_associated #0: 34 / 0.81 -> en:cebocephaly
    n1=en:major congenital anomaly | n2=en:cebocephaly | rel=r_associated | relid=0 | w=34
  18. en:major congenital anomaly -- r_associated #0: 34 / 0.81 -> en:congenital musculoskeletal defect
    n1=en:major congenital anomaly | n2=en:congenital musculoskeletal defect | rel=r_associated | relid=0 | w=34
  19. en:major congenital anomaly -- r_associated #0: 34 / 0.81 -> en:ectromelia
    n1=en:major congenital anomaly | n2=en:ectromelia | rel=r_associated | relid=0 | w=34
  20. en:major congenital anomaly -- r_associated #0: 34 / 0.81 -> en:myelomeningocele
    n1=en:major congenital anomaly | n2=en:myelomeningocele | rel=r_associated | relid=0 | w=34
  21. en:major congenital anomaly -- r_associated #0: 34 / 0.81 -> en:persistent cloaca
    n1=en:major congenital anomaly | n2=en:persistent cloaca | rel=r_associated | relid=0 | w=34
  22. en:major congenital anomaly -- r_associated #0: 34 / 0.81 -> en:thoracoschisis
    n1=en:major congenital anomaly | n2=en:thoracoschisis | rel=r_associated | relid=0 | w=34
  23. en:major congenital anomaly -- r_associated #0: 32 / 0.762 -> en:biliary atresia
    n1=en:major congenital anomaly | n2=en:biliary atresia | rel=r_associated | relid=0 | w=32
  24. en:major congenital anomaly -- r_associated #0: 32 / 0.762 -> en:bulbus cordis anomalies and anomalies of cardiac septal closure
    n1=en:major congenital anomaly | n2=en:bulbus cordis anomalies and anomalies of cardiac septal closure | rel=r_associated | relid=0 | w=32
  25. en:major congenital anomaly -- r_associated #0: 32 / 0.762 -> en:congenital macrocephaly
    n1=en:major congenital anomaly | n2=en:congenital macrocephaly | rel=r_associated | relid=0 | w=32
  26. en:major congenital anomaly -- r_associated #0: 32 / 0.762 -> en:congenital nervous system disorder
    n1=en:major congenital anomaly | n2=en:congenital nervous system disorder | rel=r_associated | relid=0 | w=32
  27. en:major congenital anomaly -- r_associated #0: 32 / 0.762 -> en:other congenital musculoskeletal deformities
    n1=en:major congenital anomaly | n2=en:other congenital musculoskeletal deformities | rel=r_associated | relid=0 | w=32
  28. en:major congenital anomaly -- r_associated #0: 32 / 0.762 -> en:prosoposchisis
    n1=en:major congenital anomaly | n2=en:prosoposchisis | rel=r_associated | relid=0 | w=32
  29. en:major congenital anomaly -- r_associated #0: 31 / 0.738 -> en:acephalostomia
    n1=en:major congenital anomaly | n2=en:acephalostomia | rel=r_associated | relid=0 | w=31
  30. en:major congenital anomaly -- r_associated #0: 31 / 0.738 -> en:aicardi syndrome
    n1=en:major congenital anomaly | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=31
  31. en:major congenital anomaly -- r_associated #0: 31 / 0.738 -> en:congenital
    n1=en:major congenital anomaly | n2=en:congenital | rel=r_associated | relid=0 | w=31
  32. en:major congenital anomaly -- r_associated #0: 31 / 0.738 -> en:congenital genitourinary abnormality
    n1=en:major congenital anomaly | n2=en:congenital genitourinary abnormality | rel=r_associated | relid=0 | w=31
  33. en:major congenital anomaly -- r_associated #0: 31 / 0.738 -> en:congenital hand and foot deformity
    n1=en:major congenital anomaly | n2=en:congenital hand and foot deformity | rel=r_associated | relid=0 | w=31
  34. en:major congenital anomaly -- r_associated #0: 31 / 0.738 -> en:encephalocele
    n1=en:major congenital anomaly | n2=en:encephalocele | rel=r_associated | relid=0 | w=31
  35. en:major congenital anomaly -- r_associated #0: 31 / 0.738 -> en:hypertelorism
    n1=en:major congenital anomaly | n2=en:hypertelorism | rel=r_associated | relid=0 | w=31
  36. en:major congenital anomaly -- r_associated #0: 31 / 0.738 -> en:omphalocele
    n1=en:major congenital anomaly | n2=en:omphalocele | rel=r_associated | relid=0 | w=31
  37. en:major congenital anomaly -- r_associated #0: 31 / 0.738 -> en:other congenital anomalies of nervous system
    n1=en:major congenital anomaly | n2=en:other congenital anomalies of nervous system | rel=r_associated | relid=0 | w=31
  38. en:major congenital anomaly -- r_associated #0: 30 / 0.714 -> en:ankyloglossia
    n1=en:major congenital anomaly | n2=en:ankyloglossia | rel=r_associated | relid=0 | w=30
  39. en:major congenital anomaly -- r_associated #0: 30 / 0.714 -> en:cleft palate
    n1=en:major congenital anomaly | n2=en:cleft palate | rel=r_associated | relid=0 | w=30
  40. en:major congenital anomaly -- r_associated #0: 30 / 0.714 -> en:craniofenestria
    n1=en:major congenital anomaly | n2=en:craniofenestria | rel=r_associated | relid=0 | w=30
  41. en:major congenital anomaly -- r_associated #0: 30 / 0.714 -> en:other and unspecified congenital anomalies
    n1=en:major congenital anomaly | n2=en:other and unspecified congenital anomalies | rel=r_associated | relid=0 | w=30
  42. en:major congenital anomaly -- r_associated #0: 30 / 0.714 -> en:polycystic kidney disease
    n1=en:major congenital anomaly | n2=en:polycystic kidney disease | rel=r_associated | relid=0 | w=30
  43. en:major congenital anomaly -- r_associated #0: 30 / 0.714 -> en:premature epiphyseal fusion
    n1=en:major congenital anomaly | n2=en:premature epiphyseal fusion | rel=r_associated | relid=0 | w=30
  44. en:major congenital anomaly -- r_associated #0: 29 / 0.69 -> en:congenital stenosis
    n1=en:major congenital anomaly | n2=en:congenital stenosis | rel=r_associated | relid=0 | w=29
  45. en:major congenital anomaly -- r_associated #0: 29 / 0.69 -> en:delayed epiphyseal fusion
    n1=en:major congenital anomaly | n2=en:delayed epiphyseal fusion | rel=r_associated | relid=0 | w=29
  46. en:major congenital anomaly -- r_associated #0: 29 / 0.69 -> en:intestinal malrotation
    n1=en:major congenital anomaly | n2=en:intestinal malrotation | rel=r_associated | relid=0 | w=29
  47. en:major congenital anomaly -- r_associated #0: 29 / 0.69 -> en:laryngeal atresia
    n1=en:major congenital anomaly | n2=en:laryngeal atresia | rel=r_associated | relid=0 | w=29
  48. en:major congenital anomaly -- r_associated #0: 29 / 0.69 -> en:nicolaides baraitser syndrome
    n1=en:major congenital anomaly | n2=en:nicolaides baraitser syndrome | rel=r_associated | relid=0 | w=29
  49. en:major congenital anomaly -- r_associated #0: 29 / 0.69 -> en:rhinocephaly
    n1=en:major congenital anomaly | n2=en:rhinocephaly | rel=r_associated | relid=0 | w=29
  50. en:major congenital anomaly -- r_associated #0: 29 / 0.69 -> en:sirenomelia
    n1=en:major congenital anomaly | n2=en:sirenomelia | rel=r_associated | relid=0 | w=29
  51. en:major congenital anomaly -- r_associated #0: 28 / 0.667 -> en:clubfoot
    n1=en:major congenital anomaly | n2=en:clubfoot | rel=r_associated | relid=0 | w=28
  52. en:major congenital anomaly -- r_associated #0: 28 / 0.667 -> en:congenital diaphragmatic hernia
    n1=en:major congenital anomaly | n2=en:congenital diaphragmatic hernia | rel=r_associated | relid=0 | w=28
  53. en:major congenital anomaly -- r_associated #0: 28 / 0.667 -> en:congenital respiratory system disorder
    n1=en:major congenital anomaly | n2=en:congenital respiratory system disorder | rel=r_associated | relid=0 | w=28
  54. en:major congenital anomaly -- r_associated #0: 28 / 0.667 -> en:congenital urinary system abnormality
    n1=en:major congenital anomaly | n2=en:congenital urinary system abnormality | rel=r_associated | relid=0 | w=28
  55. en:major congenital anomaly -- r_associated #0: 28 / 0.667 -> en:hypertrophy of clitoris
    n1=en:major congenital anomaly | n2=en:hypertrophy of clitoris | rel=r_associated | relid=0 | w=28
  56. en:major congenital anomaly -- r_associated #0: 28 / 0.667 -> en:kbg syndrome
    n1=en:major congenital anomaly | n2=en:kbg syndrome | rel=r_associated | relid=0 | w=28
  57. en:major congenital anomaly -- r_associated #0: 28 / 0.667 -> en:mental retardation
    n1=en:major congenital anomaly | n2=en:mental retardation | rel=r_associated | relid=0 | w=28
  58. en:major congenital anomaly -- r_associated #0: 28 / 0.667 -> en:neurodevelopmental anomaly
    n1=en:major congenital anomaly | n2=en:neurodevelopmental anomaly | rel=r_associated | relid=0 | w=28
  59. en:major congenital anomaly -- r_associated #0: 28 / 0.667 -> en:stomatognathic system abnormalities
    n1=en:major congenital anomaly | n2=en:stomatognathic system abnormalities | rel=r_associated | relid=0 | w=28
  60. en:major congenital anomaly -- r_associated #0: 27 / 0.643 -> en:bowen-conradi syndrome
    n1=en:major congenital anomaly | n2=en:bowen-conradi syndrome | rel=r_associated | relid=0 | w=27
  61. en:major congenital anomaly -- r_associated #0: 27 / 0.643 -> en:classical phenylketonuria
    n1=en:major congenital anomaly | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=27
  62. en:major congenital anomaly -- r_associated #0: 27 / 0.643 -> en:cleft maxilla
    n1=en:major congenital anomaly | n2=en:cleft maxilla | rel=r_associated | relid=0 | w=27
  63. en:major congenital anomaly -- r_associated #0: 27 / 0.643 -> en:congenital foot deformity
    n1=en:major congenital anomaly | n2=en:congenital foot deformity | rel=r_associated | relid=0 | w=27
  64. en:major congenital anomaly -- r_associated #0: 27 / 0.643 -> en:exencephaly
    n1=en:major congenital anomaly | n2=en:exencephaly | rel=r_associated | relid=0 | w=27
  65. en:major congenital anomaly -- r_associated #0: 27 / 0.643 -> en:lithium induced birth defect
    n1=en:major congenital anomaly | n2=en:lithium induced birth defect | rel=r_associated | relid=0 | w=27
  66. en:major congenital anomaly -- r_associated #0: 27 / 0.643 -> en:other congenital malformations of digestive system
    n1=en:major congenital anomaly | n2=en:other congenital malformations of digestive system | rel=r_associated | relid=0 | w=27
  67. en:major congenital anomaly -- r_associated #0: 27 / 0.643 -> en:sex maturation female accelerated
    n1=en:major congenital anomaly | n2=en:sex maturation female accelerated | rel=r_associated | relid=0 | w=27
  68. en:major congenital anomaly -- r_associated #0: 26 / 0.619 -> en:cheilognathopalatoschisis
    n1=en:major congenital anomaly | n2=en:cheilognathopalatoschisis | rel=r_associated | relid=0 | w=26
  69. en:major congenital anomaly -- r_associated #0: 26 / 0.619 -> en:chromosome disorder
    n1=en:major congenital anomaly | n2=en:chromosome disorder | rel=r_associated | relid=0 | w=26
  70. en:major congenital anomaly -- r_associated #0: 26 / 0.619 -> en:congenital anomaly of central nervous system
    n1=en:major congenital anomaly | n2=en:congenital anomaly of central nervous system | rel=r_associated | relid=0 | w=26
  71. en:major congenital anomaly -- r_associated #0: 26 / 0.619 -> en:congenital anomaly of gastrointestinal tract
    n1=en:major congenital anomaly | n2=en:congenital anomaly of gastrointestinal tract | rel=r_associated | relid=0 | w=26
  72. en:major congenital anomaly -- r_associated #0: 26 / 0.619 -> en:fetal postural deformity
    n1=en:major congenital anomaly | n2=en:fetal postural deformity | rel=r_associated | relid=0 | w=26
  73. en:major congenital anomaly -- r_associated #0: 26 / 0.619 -> en:hermaphrodite
    n1=en:major congenital anomaly | n2=en:hermaphrodite | rel=r_associated | relid=0 | w=26
  74. en:major congenital anomaly -- r_associated #0: 26 / 0.619 -> en:neonatal deformity
    n1=en:major congenital anomaly | n2=en:neonatal deformity | rel=r_associated | relid=0 | w=26
  75. en:major congenital anomaly -- r_associated #0: 26 / 0.619 -> en:radiation-induced disorder
    n1=en:major congenital anomaly | n2=en:radiation-induced disorder | rel=r_associated | relid=0 | w=26
  76. en:major congenital anomaly -- r_associated #0: 26 / 0.619 -> en:tetralogy of fallot
    n1=en:major congenital anomaly | n2=en:tetralogy of fallot | rel=r_associated | relid=0 | w=26
  77. en:major congenital anomaly -- r_associated #0: 25 / 0.595 -> en:cardiovascular abnormalities
    n1=en:major congenital anomaly | n2=en:cardiovascular abnormalities | rel=r_associated | relid=0 | w=25
  78. en:major congenital anomaly -- r_associated #0: 25 / 0.595 -> en:major
    n1=en:major congenital anomaly | n2=en:major | rel=r_associated | relid=0 | w=25
  79. en:major congenital anomaly -- r_associated #0: 25 / 0.595 -> en:neural tube defect
    n1=en:major congenital anomaly | n2=en:neural tube defect | rel=r_associated | relid=0 | w=25
  80. en:major congenital anomaly -- r_associated #0: 25 / 0.595 -> en:precocious puberty
    n1=en:major congenital anomaly | n2=en:precocious puberty | rel=r_associated | relid=0 | w=25
  81. en:major congenital anomaly -- r_associated #0: 25 / 0.595 -> en:transposition of great vessels
    n1=en:major congenital anomaly | n2=en:transposition of great vessels | rel=r_associated | relid=0 | w=25
  82. en:major congenital anomaly -- r_associated #0: 24 / 0.571 -> en:congenital anomalies of fetus
    n1=en:major congenital anomaly | n2=en:congenital anomalies of fetus | rel=r_associated | relid=0 | w=24
  83. en:major congenital anomaly -- r_associated #0: 24 / 0.571 -> en:congenital anomaly of neck
    n1=en:major congenital anomaly | n2=en:congenital anomaly of neck | rel=r_associated | relid=0 | w=24
  84. en:major congenital anomaly -- r_associated #0: 24 / 0.571 -> en:imperforate anus
    n1=en:major congenital anomaly | n2=en:imperforate anus | rel=r_associated | relid=0 | w=24
  85. en:major congenital anomaly -- r_associated #0: 23 / 0.548 -> en:atrial septal defect
    n1=en:major congenital anomaly | n2=en:atrial septal defect | rel=r_associated | relid=0 | w=23
  86. en:major congenital anomaly -- r_associated #0: 23 / 0.548 -> en:congenital abnormality of lower limb and/or pelvic girdle
    n1=en:major congenital anomaly | n2=en:congenital abnormality of lower limb and/or pelvic girdle | rel=r_associated | relid=0 | w=23
  87. en:major congenital anomaly -- r_associated #0: 23 / 0.548 -> en:congenital dysplasia
    n1=en:major congenital anomaly | n2=en:congenital dysplasia | rel=r_associated | relid=0 | w=23
  88. en:major congenital anomaly -- r_associated #0: 23 / 0.548 -> en:ectodermal dysplasia
    n1=en:major congenital anomaly | n2=en:ectodermal dysplasia | rel=r_associated | relid=0 | w=23
  89. en:major congenital anomaly -- r_associated #0: 22 / 0.524 -> en:congenital deformity of hip
    n1=en:major congenital anomaly | n2=en:congenital deformity of hip | rel=r_associated | relid=0 | w=22
  90. en:major congenital anomaly -- r_associated #0: 22 / 0.524 -> en:congenital deformity of knee joint
    n1=en:major congenital anomaly | n2=en:congenital deformity of knee joint | rel=r_associated | relid=0 | w=22
  91. en:major congenital anomaly -- r_associated #0: 22 / 0.524 -> malformation cardiaque
    n1=en:major congenital anomaly | n2=malformation cardiaque | rel=r_associated | relid=0 | w=22
  92. en:major congenital anomaly -- r_associated #0: 21 / 0.5 -> en:congenital hypoplasia of genital tubercle
    n1=en:major congenital anomaly | n2=en:congenital hypoplasia of genital tubercle | rel=r_associated | relid=0 | w=21
  93. en:major congenital anomaly -- r_associated #0: 21 / 0.5 -> en:gaia major congenital anomalies level of diagnostic certainty terminology
    n1=en:major congenital anomaly | n2=en:gaia major congenital anomalies level of diagnostic certainty terminology | rel=r_associated | relid=0 | w=21
  94. en:major congenital anomaly -- r_associated #0: 21 / 0.5 -> en:heart malformation
    n1=en:major congenital anomaly | n2=en:heart malformation | rel=r_associated | relid=0 | w=21
  95. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> affection cardiaque
    n1=en:major congenital anomaly | n2=affection cardiaque | rel=r_associated | relid=0 | w=20
  96. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> affection oculaire congénitale
    n1=en:major congenital anomaly | n2=affection oculaire congénitale | rel=r_associated | relid=0 | w=20
  97. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> affections cardiaques
    n1=en:major congenital anomaly | n2=affections cardiaques | rel=r_associated | relid=0 | w=20
  98. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> albinisme
    n1=en:major congenital anomaly | n2=albinisme | rel=r_associated | relid=0 | w=20
  99. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> albinisme oculocutané de type mutant jaune
    n1=en:major congenital anomaly | n2=albinisme oculocutané de type mutant jaune | rel=r_associated | relid=0 | w=20
  100. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> ancyloglosse
    n1=en:major congenital anomaly | n2=ancyloglosse | rel=r_associated | relid=0 | w=20
  101. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> ankyloglosse
    n1=en:major congenital anomaly | n2=ankyloglosse | rel=r_associated | relid=0 | w=20
  102. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> anomalie cardiaque
    n1=en:major congenital anomaly | n2=anomalie cardiaque | rel=r_associated | relid=0 | w=20
  103. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> anomalie chromosomique
    n1=en:major congenital anomaly | n2=anomalie chromosomique | rel=r_associated | relid=0 | w=20
  104. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> anomalie congénitale de l'oeil
    n1=en:major congenital anomaly | n2=anomalie congénitale de l'oeil | rel=r_associated | relid=0 | w=20
  105. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> anomalie cytogénétique
    n1=en:major congenital anomaly | n2=anomalie cytogénétique | rel=r_associated | relid=0 | w=20
  106. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> anomalie du coeur
    n1=en:major congenital anomaly | n2=anomalie du coeur | rel=r_associated | relid=0 | w=20
  107. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> anomalie du septum auriculaire
    n1=en:major congenital anomaly | n2=anomalie du septum auriculaire | rel=r_associated | relid=0 | w=20
  108. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> anormalité des chromosomes
    n1=en:major congenital anomaly | n2=anormalité des chromosomes | rel=r_associated | relid=0 | w=20
  109. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> arriération
    n1=en:major congenital anomaly | n2=arriération | rel=r_associated | relid=0 | w=20
  110. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> arriération mentale
    n1=en:major congenital anomaly | n2=arriération mentale | rel=r_associated | relid=0 | w=20
  111. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> brides amniotiques (syndrome des)
    n1=en:major congenital anomaly | n2=brides amniotiques (syndrome des) | rel=r_associated | relid=0 | w=20
  112. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> card
    n1=en:major congenital anomaly | n2=card | rel=r_associated | relid=0 | w=20
  113. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> cardiopathie
    n1=en:major congenital anomaly | n2=cardiopathie | rel=r_associated | relid=0 | w=20
  114. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> cardiopathies
    n1=en:major congenital anomaly | n2=cardiopathies | rel=r_associated | relid=0 | w=20
  115. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie
    n1=en:major congenital anomaly | n2=cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie | rel=r_associated | relid=0 | w=20
  116. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> colobome de l'iris avec ptosis, hypertélorisme et retard mental
    n1=en:major congenital anomaly | n2=colobome de l'iris avec ptosis, hypertélorisme et retard mental | rel=r_associated | relid=0 | w=20
  117. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> communication interauriculaire
    n1=en:major congenital anomaly | n2=communication interauriculaire | rel=r_associated | relid=0 | w=20
  118. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> congénital
    n1=en:major congenital anomaly | n2=congénital | rel=r_associated | relid=0 | w=20
  119. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> congenital
    n1=en:major congenital anomaly | n2=congenital | rel=r_associated | relid=0 | w=20
  120. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> congénitale
    n1=en:major congenital anomaly | n2=congénitale | rel=r_associated | relid=0 | w=20
  121. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> contractures congénitales et arachnodactylie
    n1=en:major congenital anomaly | n2=contractures congénitales et arachnodactylie | rel=r_associated | relid=0 | w=20
  122. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> crânio-sténose
    n1=en:major congenital anomaly | n2=crânio-sténose | rel=r_associated | relid=0 | w=20
  123. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> craniosténose
    n1=en:major congenital anomaly | n2=craniosténose | rel=r_associated | relid=0 | w=20
  124. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> crâniosténose
    n1=en:major congenital anomaly | n2=crâniosténose | rel=r_associated | relid=0 | w=20
  125. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> craniosynostose
    n1=en:major congenital anomaly | n2=craniosynostose | rel=r_associated | relid=0 | w=20
  126. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> crâniosynostose
    n1=en:major congenital anomaly | n2=crâniosynostose | rel=r_associated | relid=0 | w=20
  127. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> cyclopia
    n1=en:major congenital anomaly | n2=cyclopia | rel=r_associated | relid=0 | w=20
  128. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> cyclopie
    n1=en:major congenital anomaly | n2=cyclopie | rel=r_associated | relid=0 | w=20
  129. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> débilité mentale
    n1=en:major congenital anomaly | n2=débilité mentale | rel=r_associated | relid=0 | w=20
  130. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> déficience intellectuelle
    n1=en:major congenital anomaly | n2=déficience intellectuelle | rel=r_associated | relid=0 | w=20
  131. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> déficience mentale
    n1=en:major congenital anomaly | n2=déficience mentale | rel=r_associated | relid=0 | w=20
  132. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> dysplasie ectodermique
    n1=en:major congenital anomaly | n2=dysplasie ectodermique | rel=r_associated | relid=0 | w=20
  133. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental
    n1=en:major congenital anomaly | n2=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | rel=r_associated | relid=0 | w=20
  134. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> dysplasie ectodermique, ectrodactylie et dystrophie maculaire
    n1=en:major congenital anomaly | n2=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | rel=r_associated | relid=0 | w=20
  135. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie)
    n1=en:major congenital anomaly | n2=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | rel=r_associated | relid=0 | w=20
  136. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> ectopia cordis
    n1=en:major congenital anomaly | n2=ectopia cordis | rel=r_associated | relid=0 | w=20
  137. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> ectopie cardiaque
    n1=en:major congenital anomaly | n2=ectopie cardiaque | rel=r_associated | relid=0 | w=20
  138. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> elliptocytose héréditaire
    n1=en:major congenital anomaly | n2=elliptocytose héréditaire | rel=r_associated | relid=0 | w=20
  139. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:abnormality, severe teratoid
    n1=en:major congenital anomaly | n2=en:abnormality, severe teratoid | rel=r_associated | relid=0 | w=20
  140. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:adrenal cytomegaly
    n1=en:major congenital anomaly | n2=en:adrenal cytomegaly | rel=r_associated | relid=0 | w=20
  141. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:albinism
    n1=en:major congenital anomaly | n2=en:albinism | rel=r_associated | relid=0 | w=20
  142. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:amniotic band syndrome
    n1=en:major congenital anomaly | n2=en:amniotic band syndrome | rel=r_associated | relid=0 | w=20
  143. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:and mental retardation
    n1=en:major congenital anomaly | n2=en:and mental retardation | rel=r_associated | relid=0 | w=20
  144. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:aplasia, nos
    n1=en:major congenital anomaly | n2=en:aplasia, nos | rel=r_associated | relid=0 | w=20
  145. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:card
    n1=en:major congenital anomaly | n2=en:card | rel=r_associated | relid=0 | w=20
  146. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:cardiac diseases
    n1=en:major congenital anomaly | n2=en:cardiac diseases | rel=r_associated | relid=0 | w=20
  147. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:caroli disease
    n1=en:major congenital anomaly | n2=en:caroli disease | rel=r_associated | relid=0 | w=20
  148. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:caudal dysplasia
    n1=en:major congenital anomaly | n2=en:caudal dysplasia | rel=r_associated | relid=0 | w=20
  149. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:celosomy
    n1=en:major congenital anomaly | n2=en:celosomy | rel=r_associated | relid=0 | w=20
  150. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:cerebral ventriculomegaly
    n1=en:major congenital anomaly | n2=en:cerebral ventriculomegaly | rel=r_associated | relid=0 | w=20
  151. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:certain congenital musculoskeletal deformities
    n1=en:major congenital anomaly | n2=en:certain congenital musculoskeletal deformities | rel=r_associated | relid=0 | w=20
  152. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:chromosomal abnormality
    n1=en:major congenital anomaly | n2=en:chromosomal abnormality | rel=r_associated | relid=0 | w=20
  153. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:cleft lip and palate
    n1=en:major congenital anomaly | n2=en:cleft lip and palate | rel=r_associated | relid=0 | w=20
  154. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:cleft palate with cleft lip
    n1=en:major congenital anomaly | n2=en:cleft palate with cleft lip | rel=r_associated | relid=0 | w=20
  155. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:congenital abnormal fusion
    n1=en:major congenital anomaly | n2=en:congenital abnormal fusion | rel=r_associated | relid=0 | w=20
  156. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:congenital anomaly of face
    n1=en:major congenital anomaly | n2=en:congenital anomaly of face | rel=r_associated | relid=0 | w=20
  157. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:congenital cardiovascular abnormality
    n1=en:major congenital anomaly | n2=en:congenital cardiovascular abnormality | rel=r_associated | relid=0 | w=20
  158. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:congenital enlargement
    n1=en:major congenital anomaly | n2=en:congenital enlargement | rel=r_associated | relid=0 | w=20
  159. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:congenital extension deformity
    n1=en:major congenital anomaly | n2=en:congenital extension deformity | rel=r_associated | relid=0 | w=20
  160. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:congenital failure of fusion
    n1=en:major congenital anomaly | n2=en:congenital failure of fusion | rel=r_associated | relid=0 | w=20
  161. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:congenital keratoglobus
    n1=en:major congenital anomaly | n2=en:congenital keratoglobus | rel=r_associated | relid=0 | w=20
  162. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:congenital malformation syndrome
    n1=en:major congenital anomaly | n2=en:congenital malformation syndrome | rel=r_associated | relid=0 | w=20
  163. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:congenital malformation syndrome related to known exogenous cause
    n1=en:major congenital anomaly | n2=en:congenital malformation syndrome related to known exogenous cause | rel=r_associated | relid=0 | w=20
  164. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:congenital septation
    n1=en:major congenital anomaly | n2=en:congenital septation | rel=r_associated | relid=0 | w=20
  165. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:congenital vena cava abnormality
    n1=en:major congenital anomaly | n2=en:congenital vena cava abnormality | rel=r_associated | relid=0 | w=20
  166. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:conjoined twins
    n1=en:major congenital anomaly | n2=en:conjoined twins | rel=r_associated | relid=0 | w=20
  167. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:cranioschisis
    n1=en:major congenital anomaly | n2=en:cranioschisis | rel=r_associated | relid=0 | w=20
  168. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:craniostenosis
    n1=en:major congenital anomaly | n2=en:craniostenosis | rel=r_associated | relid=0 | w=20
  169. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:craniosynostosis
    n1=en:major congenital anomaly | n2=en:craniosynostosis | rel=r_associated | relid=0 | w=20
  170. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:cyclopia
    n1=en:major congenital anomaly | n2=en:cyclopia | rel=r_associated | relid=0 | w=20
  171. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:developmental immaturity
    n1=en:major congenital anomaly | n2=en:developmental immaturity | rel=r_associated | relid=0 | w=20
  172. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:embryonic cyst
    n1=en:major congenital anomaly | n2=en:embryonic cyst | rel=r_associated | relid=0 | w=20
  173. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:ethmocephaly
    n1=en:major congenital anomaly | n2=en:ethmocephaly | rel=r_associated | relid=0 | w=20
  174. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:exenkephaly
    n1=en:major congenital anomaly | n2=en:exenkephaly | rel=r_associated | relid=0 | w=20
  175. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:exomphalos
    n1=en:major congenital anomaly | n2=en:exomphalos | rel=r_associated | relid=0 | w=20
  176. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:exstrophy
    n1=en:major congenital anomaly | n2=en:exstrophy | rel=r_associated | relid=0 | w=20
  177. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:facial cleft
    n1=en:major congenital anomaly | n2=en:facial cleft | rel=r_associated | relid=0 | w=20
  178. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:failure of the mind
    n1=en:major congenital anomaly | n2=en:failure of the mind | rel=r_associated | relid=0 | w=20
  179. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:Fallot's disease
    n1=en:major congenital anomaly | n2=en:Fallot's disease | rel=r_associated | relid=0 | w=20
  180. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:feeble-mindedness
    n1=en:major congenital anomaly | n2=en:feeble-mindedness | rel=r_associated | relid=0 | w=20
  181. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:gigantism and hyperplastic visceromegaly
    n1=en:major congenital anomaly | n2=en:gigantism and hyperplastic visceromegaly | rel=r_associated | relid=0 | w=20
  182. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:hand and foot deformity
    n1=en:major congenital anomaly | n2=en:hand and foot deformity | rel=r_associated | relid=0 | w=20
  183. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:heart disease
    n1=en:major congenital anomaly | n2=en:heart disease | rel=r_associated | relid=0 | w=20
  184. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:heart diseases
    n1=en:major congenital anomaly | n2=en:heart diseases | rel=r_associated | relid=0 | w=20
  185. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:heart disorder
    n1=en:major congenital anomaly | n2=en:heart disorder | rel=r_associated | relid=0 | w=20
  186. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:hereditary elliptocytosis
    n1=en:major congenital anomaly | n2=en:hereditary elliptocytosis | rel=r_associated | relid=0 | w=20
  187. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:heterotaxy
    n1=en:major congenital anomaly | n2=en:heterotaxy | rel=r_associated | relid=0 | w=20
  188. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:heterotaxy syndrome
    n1=en:major congenital anomaly | n2=en:heterotaxy syndrome | rel=r_associated | relid=0 | w=20
  189. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:hydrencephalus
    n1=en:major congenital anomaly | n2=en:hydrencephalus | rel=r_associated | relid=0 | w=20
  190. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:hydrocephalus
    n1=en:major congenital anomaly | n2=en:hydrocephalus | rel=r_associated | relid=0 | w=20
  191. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:hypoplasia
    n1=en:major congenital anomaly | n2=en:hypoplasia | rel=r_associated | relid=0 | w=20
  192. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:hypothalamic hamartoblastoma
    n1=en:major congenital anomaly | n2=en:hypothalamic hamartoblastoma | rel=r_associated | relid=0 | w=20
  193. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:infection causing congenital anomaly
    n1=en:major congenital anomaly | n2=en:infection causing congenital anomaly | rel=r_associated | relid=0 | w=20
  194. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:known or suspected fetal abnormality affecting management of mother
    n1=en:major congenital anomaly | n2=en:known or suspected fetal abnormality affecting management of mother | rel=r_associated | relid=0 | w=20
  195. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:learning disability
    n1=en:major congenital anomaly | n2=en:learning disability | rel=r_associated | relid=0 | w=20
  196. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:limb deformities, congenital
    n1=en:major congenital anomaly | n2=en:limb deformities, congenital | rel=r_associated | relid=0 | w=20
  197. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:macroglossia
    n1=en:major congenital anomaly | n2=en:macroglossia | rel=r_associated | relid=0 | w=20
  198. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:mental deficiency
    n1=en:major congenital anomaly | n2=en:mental deficiency | rel=r_associated | relid=0 | w=20
  199. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:mental dullness
    n1=en:major congenital anomaly | n2=en:mental dullness | rel=r_associated | relid=0 | w=20
  200. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:mental handicap
    n1=en:major congenital anomaly | n2=en:mental handicap | rel=r_associated | relid=0 | w=20
  201. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:monster (disorder)
    n1=en:major congenital anomaly | n2=en:monster (disorder) | rel=r_associated | relid=0 | w=20
  202. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:nystagmus
    n1=en:major congenital anomaly | n2=en:nystagmus | rel=r_associated | relid=0 | w=20
  203. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:oligopsychia
    n1=en:major congenital anomaly | n2=en:oligopsychia | rel=r_associated | relid=0 | w=20
  204. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:ombilical hernia
    n1=en:major congenital anomaly | n2=en:ombilical hernia | rel=r_associated | relid=0 | w=20
  205. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:other specified congenital malformations
    n1=en:major congenital anomaly | n2=en:other specified congenital malformations | rel=r_associated | relid=0 | w=20
  206. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:otocephaly
    n1=en:major congenital anomaly | n2=en:otocephaly | rel=r_associated | relid=0 | w=20
  207. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:pyloric obstruction
    n1=en:major congenital anomaly | n2=en:pyloric obstruction | rel=r_associated | relid=0 | w=20
  208. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:pyloric stenosis
    n1=en:major congenital anomaly | n2=en:pyloric stenosis | rel=r_associated | relid=0 | w=20
  209. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:retardation
    n1=en:major congenital anomaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
  210. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:situs inversus
    n1=en:major congenital anomaly | n2=en:situs inversus | rel=r_associated | relid=0 | w=20
  211. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:situs inversus viscerum
    n1=en:major congenital anomaly | n2=en:situs inversus viscerum | rel=r_associated | relid=0 | w=20
  212. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:situs mutatus
    n1=en:major congenital anomaly | n2=en:situs mutatus | rel=r_associated | relid=0 | w=20
  213. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:strabismus syndrome
    n1=en:major congenital anomaly | n2=en:strabismus syndrome | rel=r_associated | relid=0 | w=20
  214. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:supernumerary structure
    n1=en:major congenital anomaly | n2=en:supernumerary structure | rel=r_associated | relid=0 | w=20
  215. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:telecanthus
    n1=en:major congenital anomaly | n2=en:telecanthus | rel=r_associated | relid=0 | w=20
  216. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:tetralogy
    n1=en:major congenital anomaly | n2=en:tetralogy | rel=r_associated | relid=0 | w=20
  217. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:tetralogy of Fallot
    n1=en:major congenital anomaly | n2=en:tetralogy of Fallot | rel=r_associated | relid=0 | w=20
  218. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:thyroid dysgenesis
    n1=en:major congenital anomaly | n2=en:thyroid dysgenesis | rel=r_associated | relid=0 | w=20
  219. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:umbilical hernia
    n1=en:major congenital anomaly | n2=en:umbilical hernia | rel=r_associated | relid=0 | w=20
  220. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:Umbilical hernia
    n1=en:major congenital anomaly | n2=en:Umbilical hernia | rel=r_associated | relid=0 | w=20
  221. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:ureterocele
    n1=en:major congenital anomaly | n2=en:ureterocele | rel=r_associated | relid=0 | w=20
  222. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> en:ventriculomeglia
    n1=en:major congenital anomaly | n2=en:ventriculomeglia | rel=r_associated | relid=0 | w=20
  223. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> exencéphalie
    n1=en:major congenital anomaly | n2=exencéphalie | rel=r_associated | relid=0 | w=20
  224. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> exomphale
    n1=en:major congenital anomaly | n2=exomphale | rel=r_associated | relid=0 | w=20
  225. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> exomphale congénitale
    n1=en:major congenital anomaly | n2=exomphale congénitale | rel=r_associated | relid=0 | w=20
  226. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> exstrophie
    n1=en:major congenital anomaly | n2=exstrophie | rel=r_associated | relid=0 | w=20
  227. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> faciès anormal, retard de croissance et retard mental
    n1=en:major congenital anomaly | n2=faciès anormal, retard de croissance et retard mental | rel=r_associated | relid=0 | w=20
  228. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> fissure faciale
    n1=en:major congenital anomaly | n2=fissure faciale | rel=r_associated | relid=0 | w=20
  229. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale
    n1=en:major congenital anomaly | n2=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | rel=r_associated | relid=0 | w=20
  230. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle
    n1=en:major congenital anomaly | n2=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | rel=r_associated | relid=0 | w=20
  231. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> hernie ombilicale
    n1=en:major congenital anomaly | n2=hernie ombilicale | rel=r_associated | relid=0 | w=20
  232. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> hernie ombilicale congénitale
    n1=en:major congenital anomaly | n2=hernie ombilicale congénitale | rel=r_associated | relid=0 | w=20
  233. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> hernies ombilicales
    n1=en:major congenital anomaly | n2=hernies ombilicales | rel=r_associated | relid=0 | w=20
  234. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> hétérotaxie
    n1=en:major congenital anomaly | n2=hétérotaxie | rel=r_associated | relid=0 | w=20
  235. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> hydrocéphalie
    n1=en:major congenital anomaly | n2=hydrocéphalie | rel=r_associated | relid=0 | w=20
  236. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> hypertélorisme
    n1=en:major congenital anomaly | n2=hypertélorisme | rel=r_associated | relid=0 | w=20
  237. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> hypertélorisme-microtie-fente faciale
    n1=en:major congenital anomaly | n2=hypertélorisme-microtie-fente faciale | rel=r_associated | relid=0 | w=20
  238. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> hypertélorisme, hypospadias, polysyndactylie (syndrome)
    n1=en:major congenital anomaly | n2=hypertélorisme, hypospadias, polysyndactylie (syndrome) | rel=r_associated | relid=0 | w=20
  239. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> hypertrophie staturale avec macroglossie et omphalocèle
    n1=en:major congenital anomaly | n2=hypertrophie staturale avec macroglossie et omphalocèle | rel=r_associated | relid=0 | w=20
  240. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> hypoplasie
    n1=en:major congenital anomaly | n2=hypoplasie | rel=r_associated | relid=0 | w=20
  241. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> imperforation anale
    n1=en:major congenital anomaly | n2=imperforation anale | rel=r_associated | relid=0 | w=20
  242. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> imperforation de l'anus
    n1=en:major congenital anomaly | n2=imperforation de l'anus | rel=r_associated | relid=0 | w=20
  243. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> jumeaux siamois
    n1=en:major congenital anomaly | n2=jumeaux siamois | rel=r_associated | relid=0 | w=20
  244. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> macroglossie
    n1=en:major congenital anomaly | n2=macroglossie | rel=r_associated | relid=0 | w=20
  245. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> maladie cardiaque
    n1=en:major congenital anomaly | n2=maladie cardiaque | rel=r_associated | relid=0 | w=20
  246. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> maladie cardiaque non précisée
    n1=en:major congenital anomaly | n2=maladie cardiaque non précisée | rel=r_associated | relid=0 | w=20
  247. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> maladie de coeur
    n1=en:major congenital anomaly | n2=maladie de coeur | rel=r_associated | relid=0 | w=20
  248. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> maladie de Roger
    n1=en:major congenital anomaly | n2=maladie de Roger | rel=r_associated | relid=0 | w=20
  249. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> maladie de roger
    n1=en:major congenital anomaly | n2=maladie de roger | rel=r_associated | relid=0 | w=20
  250. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> maladie du coeur
    n1=en:major congenital anomaly | n2=maladie du coeur | rel=r_associated | relid=0 | w=20
  251. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> maladies cardiaques
    n1=en:major congenital anomaly | n2=maladies cardiaques | rel=r_associated | relid=0 | w=20
  252. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> maladies des bandes amniotiques
    n1=en:major congenital anomaly | n2=maladies des bandes amniotiques | rel=r_associated | relid=0 | w=20
  253. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> maladies du coeur
    n1=en:major congenital anomaly | n2=maladies du coeur | rel=r_associated | relid=0 | w=20
  254. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> nanisme, retard mental, anomalies oculaires
    n1=en:major congenital anomaly | n2=nanisme, retard mental, anomalies oculaires | rel=r_associated | relid=0 | w=20
  255. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> nystagmus congénital isolé
    n1=en:major congenital anomaly | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
  256. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> oligophrénie
    n1=en:major congenital anomaly | n2=oligophrénie | rel=r_associated | relid=0 | w=20
  257. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> omphalocèle
    n1=en:major congenital anomaly | n2=omphalocèle | rel=r_associated | relid=0 | w=20
  258. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> omphalocèles
    n1=en:major congenital anomaly | n2=omphalocèles | rel=r_associated | relid=0 | w=20
  259. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> otocéphale
    n1=en:major congenital anomaly | n2=otocéphale | rel=r_associated | relid=0 | w=20
  260. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> otocéphalie
    n1=en:major congenital anomaly | n2=otocéphalie | rel=r_associated | relid=0 | w=20
  261. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> pathologie du coeur
    n1=en:major congenital anomaly | n2=pathologie du coeur | rel=r_associated | relid=0 | w=20
  262. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> phacomatose congenitale
    n1=en:major congenital anomaly | n2=phacomatose congenitale | rel=r_associated | relid=0 | w=20
  263. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> pied-bot
    n1=en:major congenital anomaly | n2=pied-bot | rel=r_associated | relid=0 | w=20
  264. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> puberté précoce
    n1=en:major congenital anomaly | n2=puberté précoce | rel=r_associated | relid=0 | w=20
  265. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> Puberté précoce
    n1=en:major congenital anomaly | n2=Puberté précoce | rel=r_associated | relid=0 | w=20
  266. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> Retard mental
    n1=en:major congenital anomaly | n2=Retard mental | rel=r_associated | relid=0 | w=20
  267. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> retard mental
    n1=en:major congenital anomaly | n2=retard mental | rel=r_associated | relid=0 | w=20
  268. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> retard mental, retard de croissance, surdité, microgénitalisme lié au sexe
    n1=en:major congenital anomaly | n2=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | rel=r_associated | relid=0 | w=20
  269. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> retardation mentale
    n1=en:major congenital anomaly | n2=retardation mentale | rel=r_associated | relid=0 | w=20
  270. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> section 3-1 maladies cardiaques
    n1=en:major congenital anomaly | n2=section 3-1 maladies cardiaques | rel=r_associated | relid=0 | w=20
  271. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> Section 3-1 Maladies cardiaques
    n1=en:major congenital anomaly | n2=Section 3-1 Maladies cardiaques | rel=r_associated | relid=0 | w=20
  272. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> sirénomélie
    n1=en:major congenital anomaly | n2=sirénomélie | rel=r_associated | relid=0 | w=20
  273. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> situs inversus
    n1=en:major congenital anomaly | n2=situs inversus | rel=r_associated | relid=0 | w=20
  274. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> sténose du pylore
    n1=en:major congenital anomaly | n2=sténose du pylore | rel=r_associated | relid=0 | w=20
  275. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> sténose pylorique
    n1=en:major congenital anomaly | n2=sténose pylorique | rel=r_associated | relid=0 | w=20
  276. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> syndrome de bride amniotique
    n1=en:major congenital anomaly | n2=syndrome de bride amniotique | rel=r_associated | relid=0 | w=20
  277. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> syndrome des brides amniotiques
    n1=en:major congenital anomaly | n2=syndrome des brides amniotiques | rel=r_associated | relid=0 | w=20
  278. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> syndrome hétérotaxique
    n1=en:major congenital anomaly | n2=syndrome hétérotaxique | rel=r_associated | relid=0 | w=20
  279. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> télécanthus-hypertélorisme-strabisme (syndrome)
    n1=en:major congenital anomaly | n2=télécanthus-hypertélorisme-strabisme (syndrome) | rel=r_associated | relid=0 | w=20
  280. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> tétralogie de Fallot
    n1=en:major congenital anomaly | n2=tétralogie de Fallot | rel=r_associated | relid=0 | w=20
  281. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> tétralogie de fallot
    n1=en:major congenital anomaly | n2=tétralogie de fallot | rel=r_associated | relid=0 | w=20
  282. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> trouble cardiaque
    n1=en:major congenital anomaly | n2=trouble cardiaque | rel=r_associated | relid=0 | w=20
  283. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> trouble chromosomique
    n1=en:major congenital anomaly | n2=trouble chromosomique | rel=r_associated | relid=0 | w=20
  284. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> urétérocèle
    n1=en:major congenital anomaly | n2=urétérocèle | rel=r_associated | relid=0 | w=20
  285. en:major congenital anomaly -- r_associated #0: 20 / 0.476 -> ventriculomégalie cérébrale
    n1=en:major congenital anomaly | n2=ventriculomégalie cérébrale | rel=r_associated | relid=0 | w=20
≈ 492 relations entrantes

  1. anormalité des chromosomes --- r_associated #0: 321 --> en:major congenital anomaly
    n1=anormalité des chromosomes | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=321
  2. en:chromosome disorder --- r_associated #0: 320 --> en:major congenital anomaly
    n1=en:chromosome disorder | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=320
  3. hernie ombilicale congénitale --- r_associated #0: 305 --> en:major congenital anomaly
    n1=hernie ombilicale congénitale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=305
  4. en:omphalocele --- r_associated #0: 302 --> en:major congenital anomaly
    n1=en:omphalocele | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=302
  5. omphalocèle --- r_associated #0: 302 --> en:major congenital anomaly
    n1=omphalocèle | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=302
  6. exomphale --- r_associated #0: 300 --> en:major congenital anomaly
    n1=exomphale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=300
  7. exomphale congénitale --- r_associated #0: 300 --> en:major congenital anomaly
    n1=exomphale congénitale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=300
  8. en:heart malformation --- r_associated #0: 299 --> en:major congenital anomaly
    n1=en:heart malformation | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=299
  9. anomalie cardiaque --- r_associated #0: 296 --> en:major congenital anomaly
    n1=anomalie cardiaque | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=296
  10. omphalocèles --- r_associated #0: 296 --> en:major congenital anomaly
    n1=omphalocèles | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=296
  11. en:heart disorder --- r_associated #0: 295 --> en:major congenital anomaly
    n1=en:heart disorder | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=295
  12. hernie ombilicale --- r_associated #0: 295 --> en:major congenital anomaly
    n1=hernie ombilicale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=295
  13. trouble cardiaque --- r_associated #0: 295 --> en:major congenital anomaly
    n1=trouble cardiaque | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=295
  14. malformation cardiaque --- r_associated #0: 294 --> en:major congenital anomaly
    n1=malformation cardiaque | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=294
  15. affection cardiaque --- r_associated #0: 290 --> en:major congenital anomaly
    n1=affection cardiaque | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=290
  16. anomalie du coeur --- r_associated #0: 290 --> en:major congenital anomaly
    n1=anomalie du coeur | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=290
  17. card --- r_associated #0: 290 --> en:major congenital anomaly
    n1=card | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=290
  18. cardiopathie --- r_associated #0: 290 --> en:major congenital anomaly
    n1=cardiopathie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=290
  19. en:heart diseases --- r_associated #0: 290 --> en:major congenital anomaly
    n1=en:heart diseases | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=290
  20. en:umbilical hernia --- r_associated #0: 290 --> en:major congenital anomaly
    n1=en:umbilical hernia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=290
  21. maladie cardiaque --- r_associated #0: 290 --> en:major congenital anomaly
    n1=maladie cardiaque | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=290
  22. maladie du coeur --- r_associated #0: 290 --> en:major congenital anomaly
    n1=maladie du coeur | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=290
  23. pathologie du coeur --- r_associated #0: 290 --> en:major congenital anomaly
    n1=pathologie du coeur | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=290
  24. maladie cardiaque non précisée --- r_associated #0: 285 --> en:major congenital anomaly
    n1=maladie cardiaque non précisée | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=285
  25. hernies ombilicales --- r_associated #0: 281 --> en:major congenital anomaly
    n1=hernies ombilicales | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=281
  26. crâniosténose --- r_associated #0: 264 --> en:major congenital anomaly
    n1=crâniosténose | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=264
  27. crânio-sténose --- r_associated #0: 263 --> en:major congenital anomaly
    n1=crânio-sténose | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=263
  28. en:craniosynostosis --- r_associated #0: 256 --> en:major congenital anomaly
    n1=en:craniosynostosis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=256
  29. craniosynostose --- r_associated #0: 255 --> en:major congenital anomaly
    n1=craniosynostose | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=255
  30. crâniosynostose --- r_associated #0: 251 --> en:major congenital anomaly
    n1=crâniosynostose | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=251
  31. section 3-1 maladies cardiaques --- r_associated #0: 250 --> en:major congenital anomaly
    n1=section 3-1 maladies cardiaques | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=250
  32. exstrophie --- r_associated #0: 225 --> en:major congenital anomaly
    n1=exstrophie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=225
  33. en:exstrophy --- r_associated #0: 223 --> en:major congenital anomaly
    n1=en:exstrophy | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=223
  34. anomalie congénitale de l'oeil --- r_associated #0: 208 --> en:major congenital anomaly
    n1=anomalie congénitale de l'oeil | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=208
  35. en:congenital eye disorder --- r_associated #0: 205 --> en:major congenital anomaly
    n1=en:congenital eye disorder | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=205
  36. trouble chromosomique --- r_associated #0: 205 --> en:major congenital anomaly
    n1=trouble chromosomique | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=205
  37. craniosténose --- r_associated #0: 185 --> en:major congenital anomaly
    n1=craniosténose | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=185
  38. hypoplasie --- r_associated #0: 184 --> en:major congenital anomaly
    n1=hypoplasie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=184
  39. affection oculaire congénitale --- r_associated #0: 180 --> en:major congenital anomaly
    n1=affection oculaire congénitale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=180
  40. en:hypoplasia --- r_associated #0: 180 --> en:major congenital anomaly
    n1=en:hypoplasia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=180
  41. maladies du coeur --- r_associated #0: 180 --> en:major congenital anomaly
    n1=maladies du coeur | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=180
  42. cardiopathies --- r_associated #0: 175 --> en:major congenital anomaly
    n1=cardiopathies | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=175
  43. affections cardiaques --- r_associated #0: 170 --> en:major congenital anomaly
    n1=affections cardiaques | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=170
  44. en:heart disease --- r_associated #0: 170 --> en:major congenital anomaly
    n1=en:heart disease | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=170
  45. maladies cardiaques --- r_associated #0: 170 --> en:major congenital anomaly
    n1=maladies cardiaques | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=170
  46. anomalie chromosomique --- r_associated #0: 160 --> en:major congenital anomaly
    n1=anomalie chromosomique | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=160
  47. en:card --- r_associated #0: 145 --> en:major congenital anomaly
    n1=en:card | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=145
  48. Retard mental --- r_associated #0: 130 --> en:major congenital anomaly
    n1=Retard mental | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=130
  49. retard mental --- r_associated #0: 130 --> en:major congenital anomaly
    n1=retard mental | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=130
  50. en:mental retardation --- r_associated #0: 129 --> en:major congenital anomaly
    n1=en:mental retardation | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=129
  51. retardation mentale --- r_associated #0: 126 --> en:major congenital anomaly
    n1=retardation mentale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=126
  52. otocéphale --- r_associated #0: 117 --> en:major congenital anomaly
    n1=otocéphale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=117
  53. situs inversus --- r_associated #0: 116 --> en:major congenital anomaly
    n1=situs inversus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=116
  54. en:situs inversus --- r_associated #0: 115 --> en:major congenital anomaly
    n1=en:situs inversus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=115
  55. tétralogie de fallot --- r_associated #0: 106 --> en:major congenital anomaly
    n1=tétralogie de fallot | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=106
  56. en:tetralogy of fallot --- r_associated #0: 104 --> en:major congenital anomaly
    n1=en:tetralogy of fallot | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=104
  57. exencéphalie --- r_associated #0: 104 --> en:major congenital anomaly
    n1=exencéphalie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=104
  58. syndrome des brides amniotiques --- r_associated #0: 101 --> en:major congenital anomaly
    n1=syndrome des brides amniotiques | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=101
  59. en:exencephaly --- r_associated #0: 100 --> en:major congenital anomaly
    n1=en:exencephaly | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=100
  60. tétralogie de Fallot --- r_associated #0: 100 --> en:major congenital anomaly
    n1=tétralogie de Fallot | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=100
  61. en:amniotic band syndrome --- r_associated #0: 98 --> en:major congenital anomaly
    n1=en:amniotic band syndrome | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=98
  62. hypertélorisme --- r_associated #0: 96 --> en:major congenital anomaly
    n1=hypertélorisme | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=96
  63. maladies des bandes amniotiques --- r_associated #0: 96 --> en:major congenital anomaly
    n1=maladies des bandes amniotiques | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=96
  64. en:tetralogy of Fallot --- r_associated #0: 95 --> en:major congenital anomaly
    n1=en:tetralogy of Fallot | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=95
  65. en:hypertelorism --- r_associated #0: 93 --> en:major congenital anomaly
    n1=en:hypertelorism | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=93
  66. ancyloglosse --- r_associated #0: 91 --> en:major congenital anomaly
    n1=ancyloglosse | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=91
  67. ankyloglosse --- r_associated #0: 91 --> en:major congenital anomaly
    n1=ankyloglosse | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=91
  68. syndrome de bride amniotique --- r_associated #0: 91 --> en:major congenital anomaly
    n1=syndrome de bride amniotique | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=91
  69. en:Umbilical hernia --- r_associated #0: 90 --> en:major congenital anomaly
    n1=en:Umbilical hernia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=90
  70. en:ankyloglossia --- r_associated #0: 90 --> en:major congenital anomaly
    n1=en:ankyloglossia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=90
  71. sténose du pylore --- r_associated #0: 90 --> en:major congenital anomaly
    n1=sténose du pylore | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=90
  72. sténose pylorique --- r_associated #0: 90 --> en:major congenital anomaly
    n1=sténose pylorique | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=90
  73. en:pyloric stenosis --- r_associated #0: 87 --> en:major congenital anomaly
    n1=en:pyloric stenosis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=87
  74. hydrocéphalie --- r_associated #0: 87 --> en:major congenital anomaly
    n1=hydrocéphalie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=87
  75. en:cerebral ventriculomegaly --- r_associated #0: 86 --> en:major congenital anomaly
    n1=en:cerebral ventriculomegaly | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=86
  76. Section 3-1 Maladies cardiaques --- r_associated #0: 85 --> en:major congenital anomaly
    n1=Section 3-1 Maladies cardiaques | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=85
  77. en:tetralogy --- r_associated #0: 85 --> en:major congenital anomaly
    n1=en:tetralogy | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=85
  78. en:ventriculomeglia --- r_associated #0: 83 --> en:major congenital anomaly
    n1=en:ventriculomeglia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=83
  79. en:Fallot's disease --- r_associated #0: 80 --> en:major congenital anomaly
    n1=en:Fallot's disease | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=80
  80. ventriculomégalie cérébrale --- r_associated #0: 79 --> en:major congenital anomaly
    n1=ventriculomégalie cérébrale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=79
  81. en:chromosomal abnormality --- r_associated #0: 75 --> en:major congenital anomaly
    n1=en:chromosomal abnormality | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=75
  82. en:pyloric obstruction --- r_associated #0: 75 --> en:major congenital anomaly
    n1=en:pyloric obstruction | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=75
  83. arriération mentale --- r_associated #0: 71 --> en:major congenital anomaly
    n1=arriération mentale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=71
  84. débilité mentale --- r_associated #0: 70 --> en:major congenital anomaly
    n1=débilité mentale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=70
  85. en:ectopia cordis --- r_associated #0: 70 --> en:major congenital anomaly
    n1=en:ectopia cordis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=70
  86. sœurs siamoises --- r_associated #0: 70 --> en:major congenital anomaly
    n1=sœurs siamoises | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=70
  87. ectopia cordis --- r_associated #0: 69 --> en:major congenital anomaly
    n1=ectopia cordis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=69
  88. en:atrial septal defect --- r_associated #0: 67 --> en:major congenital anomaly
    n1=en:atrial septal defect | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=67
  89. soeurs siamoises --- r_associated #0: 66 --> en:major congenital anomaly
    n1=soeurs siamoises | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=66
  90. anomalie du septum auriculaire --- r_associated #0: 65 --> en:major congenital anomaly
    n1=anomalie du septum auriculaire | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=65
  91. congénitale --- r_associated #0: 65 --> en:major congenital anomaly
    n1=congénitale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=65
  92. maladie du cœur --- r_associated #0: 65 --> en:major congenital anomaly
    n1=maladie du cœur | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=65
  93. urétérocèle --- r_associated #0: 65 --> en:major congenital anomaly
    n1=urétérocèle | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=65
  94. en:ureterocele --- r_associated #0: 64 --> en:major congenital anomaly
    n1=en:ureterocele | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=64
  95. en:congenital --- r_associated #0: 61 --> en:major congenital anomaly
    n1=en:congenital | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=61
  96. anomalie cytogénétique --- r_associated #0: 60 --> en:major congenital anomaly
    n1=anomalie cytogénétique | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=60
  97. en:cardiac diseases --- r_associated #0: 60 --> en:major congenital anomaly
    n1=en:cardiac diseases | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=60
  98. albinisme --- r_associated #0: 59 --> en:major congenital anomaly
    n1=albinisme | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=59
  99. en:albinism --- r_associated #0: 59 --> en:major congenital anomaly
    n1=en:albinism | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=59
  100. congénital --- r_associated #0: 57 --> en:major congenital anomaly
    n1=congénital | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=57
  101. congenital --- r_associated #0: 52 --> en:major congenital anomaly
    n1=congenital | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=52
  102. en:situs mutatus --- r_associated #0: 52 --> en:major congenital anomaly
    n1=en:situs mutatus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=52
  103. ectopie cardiaque --- r_associated #0: 51 --> en:major congenital anomaly
    n1=ectopie cardiaque | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=51
  104. en:cyclopia --- r_associated #0: 50 --> en:major congenital anomaly
    n1=en:cyclopia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=50
  105. en:exomphalos --- r_associated #0: 50 --> en:major congenital anomaly
    n1=en:exomphalos | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=50
  106. en:macroglossia --- r_associated #0: 50 --> en:major congenital anomaly
    n1=en:macroglossia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=50
  107. en:situs inversus viscerum --- r_associated #0: 50 --> en:major congenital anomaly
    n1=en:situs inversus viscerum | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=50
  108. hypertrophie staturale avec macroglossie et omphalocèle --- r_associated #0: 50 --> en:major congenital anomaly
    n1=hypertrophie staturale avec macroglossie et omphalocèle | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=50
  109. en:heterotaxy syndrome --- r_associated #0: 49 --> en:major congenital anomaly
    n1=en:heterotaxy syndrome | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=49
  110. télécanthus-hypertélorisme-strabisme (syndrome) --- r_associated #0: 48 --> en:major congenital anomaly
    n1=télécanthus-hypertélorisme-strabisme (syndrome) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=48
  111. cyclopia --- r_associated #0: 47 --> en:major congenital anomaly
    n1=cyclopia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=47
  112. retard mental, retard de croissance, surdité, microgénitalisme lié au sexe --- r_associated #0: 47 --> en:major congenital anomaly
    n1=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=47
  113. cyclopie --- r_associated #0: 45 --> en:major congenital anomaly
    n1=cyclopie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=45
  114. en:hydrencephalus --- r_associated #0: 44 --> en:major congenital anomaly
    n1=en:hydrencephalus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=44
  115. hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle --- r_associated #0: 44 --> en:major congenital anomaly
    n1=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=44
  116. en:kbg syndrome --- r_associated #0: 43 --> en:major congenital anomaly
    n1=en:kbg syndrome | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=43
  117. en:limb deformities, congenital --- r_associated #0: 43 --> en:major congenital anomaly
    n1=en:limb deformities, congenital | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=43
  118. en:certain congenital musculoskeletal deformities --- r_associated #0: 42 --> en:major congenital anomaly
    n1=en:certain congenital musculoskeletal deformities | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=42
  119. hypertélorisme-microtie-fente faciale --- r_associated #0: 42 --> en:major congenital anomaly
    n1=hypertélorisme-microtie-fente faciale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=42
  120. imperforation de l'anus --- r_associated #0: 42 --> en:major congenital anomaly
    n1=imperforation de l'anus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=42
  121. puberté précoce --- r_associated #0: 42 --> en:major congenital anomaly
    n1=puberté précoce | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=42
  122. dysplasie ectodermique --- r_associated #0: 41 --> en:major congenital anomaly
    n1=dysplasie ectodermique | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=41
  123. en:congenital extension deformity --- r_associated #0: 41 --> en:major congenital anomaly
    n1=en:congenital extension deformity | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=41
  124. en:stomatognathic system abnormalities --- r_associated #0: 41 --> en:major congenital anomaly
    n1=en:stomatognathic system abnormalities | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=41
  125. hétérotaxie --- r_associated #0: 41 --> en:major congenital anomaly
    n1=hétérotaxie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=41
  126. imperforation anale --- r_associated #0: 41 --> en:major congenital anomaly
    n1=imperforation anale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=41
  127. macroglossie --- r_associated #0: 41 --> en:major congenital anomaly
    n1=macroglossie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=41
  128. sirénomélie --- r_associated #0: 41 --> en:major congenital anomaly
    n1=sirénomélie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=41
  129. en:congenital enlargement --- r_associated #0: 40 --> en:major congenital anomaly
    n1=en:congenital enlargement | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=40
  130. en:heterotaxy --- r_associated #0: 40 --> en:major congenital anomaly
    n1=en:heterotaxy | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=40
  131. en:precocious puberty --- r_associated #0: 40 --> en:major congenital anomaly
    n1=en:precocious puberty | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=40
  132. maladie de cœur --- r_associated #0: 40 --> en:major congenital anomaly
    n1=maladie de cœur | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=40
  133. maladie de coeur --- r_associated #0: 40 --> en:major congenital anomaly
    n1=maladie de coeur | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=40
  134. nystagmus congénital isolé --- r_associated #0: 40 --> en:major congenital anomaly
    n1=nystagmus congénital isolé | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=40
  135. Puberté précoce --- r_associated #0: 39 --> en:major congenital anomaly
    n1=Puberté précoce | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=39
  136. en:imperforate anus --- r_associated #0: 39 --> en:major congenital anomaly
    n1=en:imperforate anus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=39
  137. en:ombilical hernia --- r_associated #0: 39 --> en:major congenital anomaly
    n1=en:ombilical hernia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=39
  138. maladie de Roger --- r_associated #0: 39 --> en:major congenital anomaly
    n1=maladie de Roger | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=39
  139. dysplasie ectodermique, ectrodactylie et dystrophie maculaire --- r_associated #0: 38 --> en:major congenital anomaly
    n1=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=38
  140. hypertélorisme, hypospadias, polysyndactylie (syndrome) --- r_associated #0: 38 --> en:major congenital anomaly
    n1=hypertélorisme, hypospadias, polysyndactylie (syndrome) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=38
  141. déficience intellectuelle --- r_associated #0: 37 --> en:major congenital anomaly
    n1=déficience intellectuelle | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=37
  142. ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) --- r_associated #0: 37 --> en:major congenital anomaly
    n1=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=37
  143. en:congenital urinary system abnormality --- r_associated #0: 37 --> en:major congenital anomaly
    n1=en:congenital urinary system abnormality | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=37
  144. en:ectodermal dysplasia --- r_associated #0: 37 --> en:major congenital anomaly
    n1=en:ectodermal dysplasia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=37
  145. en:sirenomelia --- r_associated #0: 37 --> en:major congenital anomaly
    n1=en:sirenomelia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=37
  146. en:telecanthus --- r_associated #0: 37 --> en:major congenital anomaly
    n1=en:telecanthus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=37
  147. hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale --- r_associated #0: 37 --> en:major congenital anomaly
    n1=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=37
  148. phacomatose congenitale --- r_associated #0: 37 --> en:major congenital anomaly
    n1=phacomatose congenitale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=37
  149. en:adrenal cytomegaly --- r_associated #0: 36 --> en:major congenital anomaly
    n1=en:adrenal cytomegaly | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=36
  150. en:gigantism and hyperplastic visceromegaly --- r_associated #0: 36 --> en:major congenital anomaly
    n1=en:gigantism and hyperplastic visceromegaly | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=36
  151. en:supernumerary structure --- r_associated #0: 36 --> en:major congenital anomaly
    n1=en:supernumerary structure | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=36
  152. en:thyroid dysgenesis --- r_associated #0: 36 --> en:major congenital anomaly
    n1=en:thyroid dysgenesis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=36
  153. en:ventricular septal defect --- r_associated #0: 36 --> en:major congenital anomaly
    n1=en:ventricular septal defect | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=36
  154. faciès anormal, retard de croissance et retard mental --- r_associated #0: 36 --> en:major congenital anomaly
    n1=faciès anormal, retard de croissance et retard mental | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=36
  155. en:aplasia, nos --- r_associated #0: 35 --> en:major congenital anomaly
    n1=en:aplasia, nos | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=35
  156. en:congenital anomaly of face --- r_associated #0: 35 --> en:major congenital anomaly
    n1=en:congenital anomaly of face | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=35
  157. en:cranioschisis --- r_associated #0: 35 --> en:major congenital anomaly
    n1=en:cranioschisis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=35
  158. en:embryonic cyst --- r_associated #0: 35 --> en:major congenital anomaly
    n1=en:embryonic cyst | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=35
  159. en:mental deficiency --- r_associated #0: 35 --> en:major congenital anomaly
    n1=en:mental deficiency | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=35
  160. en:neurodevelopmental anomaly --- r_associated #0: 35 --> en:major congenital anomaly
    n1=en:neurodevelopmental anomaly | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=35
  161. en:other congenital malformations of digestive system --- r_associated #0: 35 --> en:major congenital anomaly
    n1=en:other congenital malformations of digestive system | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=35
  162. en:other specified congenital malformations --- r_associated #0: 35 --> en:major congenital anomaly
    n1=en:other specified congenital malformations | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=35
  163. dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental --- r_associated #0: 34 --> en:major congenital anomaly
    n1=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=34
  164. en:caroli disease --- r_associated #0: 34 --> en:major congenital anomaly
    n1=en:caroli disease | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=34
  165. en:congenital anomalies of fetus --- r_associated #0: 34 --> en:major congenital anomaly
    n1=en:congenital anomalies of fetus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=34
  166. en:congenital failure of fusion --- r_associated #0: 34 --> en:major congenital anomaly
    n1=en:congenital failure of fusion | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=34
  167. en:congenital septation --- r_associated #0: 34 --> en:major congenital anomaly
    n1=en:congenital septation | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=34
  168. en:congenital systemic disorder --- r_associated #0: 34 --> en:major congenital anomaly
    n1=en:congenital systemic disorder | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=34
  169. en:cryptophthalmia --- r_associated #0: 34 --> en:major congenital anomaly
    n1=en:cryptophthalmia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=34
  170. en:hereditary elliptocytosis --- r_associated #0: 34 --> en:major congenital anomaly
    n1=en:hereditary elliptocytosis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=34
  171. en:other and unspecified congenital anomalies --- r_associated #0: 34 --> en:major congenital anomaly
    n1=en:other and unspecified congenital anomalies | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=34
  172. en:thoracoschisis --- r_associated #0: 34 --> en:major congenital anomaly
    n1=en:thoracoschisis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=34
  173. fissure faciale --- r_associated #0: 34 --> en:major congenital anomaly
    n1=fissure faciale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=34
  174. en:exenkephaly --- r_associated #0: 33 --> en:major congenital anomaly
    n1=en:exenkephaly | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=33
  175. en:aicardi syndrome --- r_associated #0: 32 --> en:major congenital anomaly
    n1=en:aicardi syndrome | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=32
  176. en:cleft palate with cleft lip --- r_associated #0: 32 --> en:major congenital anomaly
    n1=en:cleft palate with cleft lip | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=32
  177. en:congenital cardiovascular abnormality --- r_associated #0: 32 --> en:major congenital anomaly
    n1=en:congenital cardiovascular abnormality | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=32
  178. en:congenital malformation syndrome --- r_associated #0: 32 --> en:major congenital anomaly
    n1=en:congenital malformation syndrome | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=32
  179. en:delayed epiphyseal fusion --- r_associated #0: 32 --> en:major congenital anomaly
    n1=en:delayed epiphyseal fusion | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=32
  180. en:laryngeal atresia --- r_associated #0: 32 --> en:major congenital anomaly
    n1=en:laryngeal atresia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=32
  181. elliptocytose héréditaire --- r_associated #0: 31 --> en:major congenital anomaly
    n1=elliptocytose héréditaire | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=31
  182. en:congenital musculoskeletal defect --- r_associated #0: 31 --> en:major congenital anomaly
    n1=en:congenital musculoskeletal defect | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=31
  183. en:facial cleft --- r_associated #0: 31 --> en:major congenital anomaly
    n1=en:facial cleft | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=31
  184. en:hydrocephalus --- r_associated #0: 31 --> en:major congenital anomaly
    n1=en:hydrocephalus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=31
  185. nanisme, retard mental, anomalies oculaires --- r_associated #0: 31 --> en:major congenital anomaly
    n1=nanisme, retard mental, anomalies oculaires | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=31
  186. oligophrénie --- r_associated #0: 31 --> en:major congenital anomaly
    n1=oligophrénie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=31
  187. troubles du myocarde --- r_associated #0: 31 --> en:major congenital anomaly
    n1=troubles du myocarde | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=31
  188. arriération --- r_associated #0: 30 --> en:major congenital anomaly
    n1=arriération | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  189. colobome de l'iris avec ptosis, hypertélorisme et retard mental --- r_associated #0: 30 --> en:major congenital anomaly
    n1=colobome de l'iris avec ptosis, hypertélorisme et retard mental | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  190. en:and mental retardation --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:and mental retardation | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  191. en:cardiovascular abnormalities --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:cardiovascular abnormalities | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  192. en:cleft lip and palate --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:cleft lip and palate | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  193. en:cleft maxilla --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:cleft maxilla | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  194. en:congenital abnormality of lower limb and/or pelvic girdle --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:congenital abnormality of lower limb and/or pelvic girdle | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  195. en:congenital hypoplasia of genital tubercle --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:congenital hypoplasia of genital tubercle | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  196. en:congenital malformation syndrome related to known exogenous cause --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:congenital malformation syndrome related to known exogenous cause | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  197. en:congenital nervous system disorder --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:congenital nervous system disorder | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  198. en:craniostenosis --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:craniostenosis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  199. en:developmental immaturity --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:developmental immaturity | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  200. en:ethmocephaly --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:ethmocephaly | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  201. en:hand and foot deformity --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:hand and foot deformity | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  202. en:hypertrophy of clitoris --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:hypertrophy of clitoris | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  203. en:hypothalamic hamartoblastoma --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:hypothalamic hamartoblastoma | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  204. en:infection causing congenital anomaly --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:infection causing congenital anomaly | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  205. en:learning disability --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:learning disability | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  206. en:lymphatic abnormalities --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:lymphatic abnormalities | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  207. en:mental dullness --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:mental dullness | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  208. en:mental handicap --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:mental handicap | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  209. en:other congenital anomalies of nervous system --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:other congenital anomalies of nervous system | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  210. en:retardation --- r_associated #0: 30 --> en:major congenital anomaly
    n1=en:retardation | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  211. jumeaux conjoints --- r_associated #0: 30 --> en:major congenital anomaly
    n1=jumeaux conjoints | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  212. maladie de roger --- r_associated #0: 30 --> en:major congenital anomaly
    n1=maladie de roger | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
  213. albinisme oculocutané de type mutant jaune --- r_associated #0: 29 --> en:major congenital anomaly
    n1=albinisme oculocutané de type mutant jaune | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  214. cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie --- r_associated #0: 29 --> en:major congenital anomaly
    n1=cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  215. déficience mentale --- r_associated #0: 29 --> en:major congenital anomaly
    n1=déficience mentale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  216. en:abnormalities, drug-induced --- r_associated #0: 29 --> en:major congenital anomaly
    n1=en:abnormalities, drug-induced | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  217. en:clubfoot --- r_associated #0: 29 --> en:major congenital anomaly
    n1=en:clubfoot | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  218. en:congenital deformity of hip --- r_associated #0: 29 --> en:major congenital anomaly
    n1=en:congenital deformity of hip | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  219. en:congenital keratoglobus --- r_associated #0: 29 --> en:major congenital anomaly
    n1=en:congenital keratoglobus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  220. en:congenital macrocephaly --- r_associated #0: 29 --> en:major congenital anomaly
    n1=en:congenital macrocephaly | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  221. en:congenital stenosis --- r_associated #0: 29 --> en:major congenital anomaly
    n1=en:congenital stenosis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  222. en:feeble-mindedness --- r_associated #0: 29 --> en:major congenital anomaly
    n1=en:feeble-mindedness | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  223. en:intestinal malrotation --- r_associated #0: 29 --> en:major congenital anomaly
    n1=en:intestinal malrotation | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  224. en:monster (disorder) --- r_associated #0: 29 --> en:major congenital anomaly
    n1=en:monster (disorder) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  225. en:nicolaides baraitser syndrome --- r_associated #0: 29 --> en:major congenital anomaly
    n1=en:nicolaides baraitser syndrome | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  226. en:transposition of great vessels --- r_associated #0: 29 --> en:major congenital anomaly
    n1=en:transposition of great vessels | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  227. hypopituitarisme --- r_associated #0: 29 --> en:major congenital anomaly
    n1=hypopituitarisme | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  228. syndrome hétérotaxique --- r_associated #0: 29 --> en:major congenital anomaly
    n1=syndrome hétérotaxique | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=29
  229. contractures congénitales et arachnodactylie --- r_associated #0: 28 --> en:major congenital anomaly
    n1=contractures congénitales et arachnodactylie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=28
  230. en:abnormality, severe teratoid --- r_associated #0: 28 --> en:major congenital anomaly
    n1=en:abnormality, severe teratoid | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=28
  231. en:caudal dysplasia --- r_associated #0: 28 --> en:major congenital anomaly
    n1=en:caudal dysplasia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=28
  232. Déficience intellectuelle --- r_associated #0: 27 --> en:major congenital anomaly
    n1=Déficience intellectuelle | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=27
  233. brides amniotiques (syndrome des) --- r_associated #0: 27 --> en:major congenital anomaly
    n1=brides amniotiques (syndrome des) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=27
  234. en:congenital abnormal fusion --- r_associated #0: 27 --> en:major congenital anomaly
    n1=en:congenital abnormal fusion | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=27
  235. en:congenital anomaly of neck --- r_associated #0: 27 --> en:major congenital anomaly
    n1=en:congenital anomaly of neck | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=27
  236. en:congenital deformity of knee joint --- r_associated #0: 27 --> en:major congenital anomaly
    n1=en:congenital deformity of knee joint | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=27
  237. en:congenital vena cava abnormality --- r_associated #0: 27 --> en:major congenital anomaly
    n1=en:congenital vena cava abnormality | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=27
  238. en:failure of the mind --- r_associated #0: 27 --> en:major congenital anomaly
    n1=en:failure of the mind | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=27
  239. en:known or suspected fetal abnormality affecting management of mother --- r_associated #0: 27 --> en:major congenital anomaly
    n1=en:known or suspected fetal abnormality affecting management of mother | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=27
  240. en:oligopsychia --- r_associated #0: 27 --> en:major congenital anomaly
    n1=en:oligopsychia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=27
  241. en:strabismus syndrome --- r_associated #0: 27 --> en:major congenital anomaly
    n1=en:strabismus syndrome | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=27
  242. pied-bot --- r_associated #0: 27 --> en:major congenital anomaly
    n1=pied-bot | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=27
  243. communication inter-auriculaire --- r_associated #0: 26 --> en:major congenital anomaly
    n1=communication inter-auriculaire | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  244. communication interauriculaire --- r_associated #0: 26 --> en:major congenital anomaly
    n1=communication interauriculaire | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  245. en:acephalostomia --- r_associated #0: 26 --> en:major congenital anomaly
    n1=en:acephalostomia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  246. en:bowen-conradi syndrome --- r_associated #0: 26 --> en:major congenital anomaly
    n1=en:bowen-conradi syndrome | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  247. en:celosomy --- r_associated #0: 26 --> en:major congenital anomaly
    n1=en:celosomy | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  248. en:congenital dysplasia --- r_associated #0: 26 --> en:major congenital anomaly
    n1=en:congenital dysplasia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  249. en:congenital foot deformity --- r_associated #0: 26 --> en:major congenital anomaly
    n1=en:congenital foot deformity | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  250. en:conjoined twins --- r_associated #0: 26 --> en:major congenital anomaly
    n1=en:conjoined twins | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  251. en:fetal postural deformity --- r_associated #0: 26 --> en:major congenital anomaly
    n1=en:fetal postural deformity | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  252. en:gaia major congenital anomalies level of diagnostic certainty terminology --- r_associated #0: 26 --> en:major congenital anomaly
    n1=en:gaia major congenital anomalies level of diagnostic certainty terminology | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  253. en:neural tube defect --- r_associated #0: 26 --> en:major congenital anomaly
    n1=en:neural tube defect | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  254. en:nystagmus --- r_associated #0: 26 --> en:major congenital anomaly
    n1=en:nystagmus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  255. en:otocephaly --- r_associated #0: 26 --> en:major congenital anomaly
    n1=en:otocephaly | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  256. en:persistent cloaca --- r_associated #0: 26 --> en:major congenital anomaly
    n1=en:persistent cloaca | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  257. en:radiation-induced disorder --- r_associated #0: 26 --> en:major congenital anomaly
    n1=en:radiation-induced disorder | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  258. jumeaux siamois --- r_associated #0: 26 --> en:major congenital anomaly
    n1=jumeaux siamois | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  259. otocéphalie --- r_associated #0: 26 --> en:major congenital anomaly
    n1=otocéphalie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=26
  260. albinisme avec pigmentation minime --- r_associated #0: 25 --> en:major congenital anomaly
    n1=albinisme avec pigmentation minime | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=25
  261. atrésie laryngée --- r_associated #0: 25 --> en:major congenital anomaly
    n1=atrésie laryngée | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=25
  262. en:Siamese twins --- r_associated #0: 25 --> en:major congenital anomaly
    n1=en:Siamese twins | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=25
  263. en:cheilognathoschisis --- r_associated #0: 25 --> en:major congenital anomaly
    n1=en:cheilognathoschisis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=25
  264. en:hypopituitarism --- r_associated #0: 25 --> en:major congenital anomaly
    n1=en:hypopituitarism | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=25
  265. en:juvenile cataract --- r_associated #0: 25 --> en:major congenital anomaly
    n1=en:juvenile cataract | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=25
  266. en:megaloglossia --- r_associated #0: 25 --> en:major congenital anomaly
    n1=en:megaloglossia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=25
  267. en:morosis --- r_associated #0: 25 --> en:major congenital anomaly
    n1=en:morosis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=25
  268. frères siamois --- r_associated #0: 25 --> en:major congenital anomaly
    n1=frères siamois | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=25
  269. télécanthus --- r_associated #0: 25 --> en:major congenital anomaly
    n1=télécanthus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=25
  270. en:X-linked --- r_associated #0: 24 --> en:major congenital anomaly
    n1=en:X-linked | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=24
  271. en:anal imperforation --- r_associated #0: 24 --> en:major congenital anomaly
    n1=en:anal imperforation | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=24
  272. en:cerebellar atrophy --- r_associated #0: 24 --> en:major congenital anomaly
    n1=en:cerebellar atrophy | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=24
  273. en:monopia --- r_associated #0: 24 --> en:major congenital anomaly
    n1=en:monopia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=24
  274. en:proctatresia --- r_associated #0: 24 --> en:major congenital anomaly
    n1=en:proctatresia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=24
  275. en:umbilical hiatus --- r_associated #0: 24 --> en:major congenital anomaly
    n1=en:umbilical hiatus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=24
  276. en:with growth retardation --- r_associated #0: 24 --> en:major congenital anomaly
    n1=en:with growth retardation | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=24
  277. situs mutatus --- r_associated #0: 24 --> en:major congenital anomaly
    n1=situs mutatus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=24
  278. cataracte-atrophie du cervelet-myopathie --- r_associated #0: 23 --> en:major congenital anomaly
    n1=cataracte-atrophie du cervelet-myopathie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=23
  279. en:oligergasia --- r_associated #0: 23 --> en:major congenital anomaly
    n1=en:oligergasia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=23
  280. albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception --- r_associated #0: 22 --> en:major congenital anomaly
    n1=albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=22
  281. cranioschisis --- r_associated #0: 22 --> en:major congenital anomaly
    n1=cranioschisis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=22
  282. en:absent corpus callosum --- r_associated #0: 22 --> en:major congenital anomaly
    n1=en:absent corpus callosum | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=22
  283. en:chromosomal aberration --- r_associated #0: 22 --> en:major congenital anomaly
    n1=en:chromosomal aberration | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=22
  284. en:deafness --- r_associated #0: 22 --> en:major congenital anomaly
    n1=en:deafness | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=22
  285. en:diaphragmatic hernia --- r_associated #0: 22 --> en:major congenital anomaly
    n1=en:diaphragmatic hernia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=22
  286. en:exumbilication --- r_associated #0: 22 --> en:major congenital anomaly
    n1=en:exumbilication | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=22
  287. en:hematomphalus --- r_associated #0: 22 --> en:major congenital anomaly
    n1=en:hematomphalus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=22
  288. jumeaux fusionnés --- r_associated #0: 22 --> en:major congenital anomaly
    n1=jumeaux fusionnés | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=22
  289. communication interventriculaire --- r_associated #0: 21 --> en:major congenital anomaly
    n1=communication interventriculaire | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=21
  290. en:and microgenitalism --- r_associated #0: 21 --> en:major congenital anomaly
    n1=en:and microgenitalism | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=21
  291. en:dwarfism --- r_associated #0: 21 --> en:major congenital anomaly
    n1=en:dwarfism | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=21
  292. en:heart ectopy --- r_associated #0: 21 --> en:major congenital anomaly
    n1=en:heart ectopy | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=21
  293. en:oligophrenia --- r_associated #0: 21 --> en:major congenital anomaly
    n1=en:oligophrenia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=21
  294. situs inversus viscerum --- r_associated #0: 21 --> en:major congenital anomaly
    n1=situs inversus viscerum | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=21
  295. troubles endocriniens, épilepsie et déficience mentale --- r_associated #0: 21 --> en:major congenital anomaly
    n1=troubles endocriniens, épilepsie et déficience mentale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=21
  296. en:amastia --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:amastia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  297. en:anomaly congenital special senses --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:anomaly congenital special senses | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  298. en:biliary atresia --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:biliary atresia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  299. en:branchial cleft remnant --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:branchial cleft remnant | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  300. en:bulbus cordis anomalies and anomalies of cardiac septal closure --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:bulbus cordis anomalies and anomalies of cardiac septal closure | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  301. en:cebocephaly --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:cebocephaly | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  302. en:cheilognathopalatoschisis --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:cheilognathopalatoschisis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  303. en:classical phenylketonuria --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:classical phenylketonuria | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  304. en:cleft jaw --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:cleft jaw | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  305. en:cleft palate --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:cleft palate | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  306. en:congenital anomaly of central nervous system --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:congenital anomaly of central nervous system | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  307. en:congenital anomaly of gastrointestinal tract --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:congenital anomaly of gastrointestinal tract | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  308. en:congenital diaphragmatic hernia --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:congenital diaphragmatic hernia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  309. en:congenital disruption --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:congenital disruption | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  310. en:congenital genitourinary abnormality --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:congenital genitourinary abnormality | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  311. en:congenital hand and foot deformity --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:congenital hand and foot deformity | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  312. en:congenital morphologic anomaly --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:congenital morphologic anomaly | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  313. en:congenital respiratory system disorder --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:congenital respiratory system disorder | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  314. en:connatal disorder --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:connatal disorder | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  315. en:craniofenestria --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:craniofenestria | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  316. en:ectromelia --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:ectromelia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  317. en:encephalocele --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:encephalocele | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  318. en:gastroschisis --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:gastroschisis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  319. en:hermaphrodite --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:hermaphrodite | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  320. en:lithium induced birth defect --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:lithium induced birth defect | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  321. en:myelomeningocele --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:myelomeningocele | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  322. en:neonatal deformity --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:neonatal deformity | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  323. en:other congenital musculoskeletal deformities --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:other congenital musculoskeletal deformities | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  324. en:polycystic kidney disease --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:polycystic kidney disease | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  325. en:premature epiphyseal fusion --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:premature epiphyseal fusion | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  326. en:prosoposchisis --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:prosoposchisis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  327. en:rhinocephaly --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:rhinocephaly | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  328. en:sex maturation female accelerated --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:sex maturation female accelerated | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  329. en:spina bifida --- r_associated #0: 20 --> en:major congenital anomaly
    n1=en:spina bifida | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=20
  330. Albert (position d') --- r_associated #0: 15 --> en:major congenital anomaly
    n1=Albert (position d') | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  331. Anitschkow (cellule de) --- r_associated #0: 15 --> en:major congenital anomaly
    n1=Anitschkow (cellule de) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  332. Arrhenius (loi d') --- r_associated #0: 15 --> en:major congenital anomaly
    n1=Arrhenius (loi d') | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  333. CARD --- r_associated #0: 15 --> en:major congenital anomaly
    n1=CARD | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  334. Elliott (lambeau d') --- r_associated #0: 15 --> en:major congenital anomaly
    n1=Elliott (lambeau d') | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  335. Malformation cardiaque --- r_associated #0: 15 --> en:major congenital anomaly
    n1=Malformation cardiaque | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  336. cyclope (oeil) --- r_associated #0: 15 --> en:major congenital anomaly
    n1=cyclope (oeil) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  337. ectodermitis erosiva pluriorificialis --- r_associated #0: 15 --> en:major congenital anomaly
    n1=ectodermitis erosiva pluriorificialis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  338. ectodermose --- r_associated #0: 15 --> en:major congenital anomaly
    n1=ectodermose | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  339. ectodermose érosive pluriorificielle de Fiessinger-Rendu --- r_associated #0: 15 --> en:major congenital anomaly
    n1=ectodermose érosive pluriorificielle de Fiessinger-Rendu | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  340. ectoenzyme --- r_associated #0: 15 --> en:major congenital anomaly
    n1=ectoenzyme | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  341. ectomie --- r_associated #0: 15 --> en:major congenital anomaly
    n1=ectomie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  342. ectomorphie --- r_associated #0: 15 --> en:major congenital anomaly
    n1=ectomorphie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  343. ectoparasite --- r_associated #0: 15 --> en:major congenital anomaly
    n1=ectoparasite | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  344. ectoparasitose --- r_associated #0: 15 --> en:major congenital anomaly
    n1=ectoparasitose | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  345. exécutives (fonctions) --- r_associated #0: 15 --> en:major congenital anomaly
    n1=exécutives (fonctions) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  346. handicap mental --- r_associated #0: 15 --> en:major congenital anomaly
    n1=handicap mental | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  347. hydrocèle (cure chirurgicale d') --- r_associated #0: 15 --> en:major congenital anomaly
    n1=hydrocèle (cure chirurgicale d') | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=15
  348. Albinisme --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Albinisme | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  349. Anomalie chromosomique --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Anomalie chromosomique | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  350. CONGÉNITALE --- r_associated #0: 10 --> en:major congenital anomaly
    n1=CONGÉNITALE | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  351. Card --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Card | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  352. Cardiopathie --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Cardiopathie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  353. Communication interauriculaire --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Communication interauriculaire | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  354. Craniosynostose --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Craniosynostose | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  355. Ectoparasite --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Ectoparasite | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  356. Haltia-Santavuori (maladie de) --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Haltia-Santavuori (maladie de) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  357. Hernie ombilicale --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Hernie ombilicale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  358. Hydrocéphalie --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Hydrocéphalie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  359. Hypertélorisme --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Hypertélorisme | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  360. Hypoplasie --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Hypoplasie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  361. Jumeaux siamois --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Jumeaux siamois | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  362. Macroglossie --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Macroglossie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  363. Maladies cardiaques --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Maladies cardiaques | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  364. Roger (maladie de) --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Roger (maladie de) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  365. Sipple (syndrome de) --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Sipple (syndrome de) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  366. Situs inversus --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Situs inversus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  367. Völker-Dieben (atrophie optique liée au sexe de) --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Völker-Dieben (atrophie optique liée au sexe de) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  368. Went (atrophie optique liée au sexe de) --- r_associated #0: 10 --> en:major congenital anomaly
    n1=Went (atrophie optique liée au sexe de) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  369. aberration chromosomique --- r_associated #0: 10 --> en:major congenital anomaly
    n1=aberration chromosomique | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  370. cheilognathopalatoschisis --- r_associated #0: 10 --> en:major congenital anomaly
    n1=cheilognathopalatoschisis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  371. déficit intellectuel --- r_associated #0: 10 --> en:major congenital anomaly
    n1=déficit intellectuel | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  372. ectopie des procès ciliaires --- r_associated #0: 10 --> en:major congenital anomaly
    n1=ectopie des procès ciliaires | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  373. ectopie du cristallin --- r_associated #0: 10 --> en:major congenital anomaly
    n1=ectopie du cristallin | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  374. en:Albert's position --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:Albert's position | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  375. en:Anitschkow's cell --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:Anitschkow's cell | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  376. en:Arrhenius'law --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:Arrhenius'law | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  377. en:Elliott lateral flap --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:Elliott lateral flap | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  378. en:Siamese twin brothers --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:Siamese twin brothers | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  379. en:and growth retardation --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:and growth retardation | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  380. en:and postaxil polydactylie --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:and postaxil polydactylie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  381. en:and sensorineural deafness --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:and sensorineural deafness | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  382. en:atresia ani --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:atresia ani | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  383. en:chromosomal disorder --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:chromosomal disorder | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  384. en:conjoined twin brothers --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:conjoined twin brothers | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  385. en:conjoints twins --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:conjoints twins | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  386. en:contractural arachnodactyly --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:contractural arachnodactyly | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  387. en:cyclops eye --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:cyclops eye | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  388. en:ectodermosis --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:ectodermosis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  389. en:ectodermosis erosiva pluriorificialis --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:ectodermosis erosiva pluriorificialis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  390. en:ectoenzyme --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:ectoenzyme | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  391. en:ectoparasite --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:ectoparasite | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  392. en:ectoparasitosis --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:ectoparasitosis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  393. en:ectrodactyly and macular dystrophy --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:ectrodactyly and macular dystrophy | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  394. en:endocrine disorder --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:endocrine disorder | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  395. en:executive functions --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:executive functions | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  396. en:eye abnormality --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:eye abnormality | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  397. en:facial clefting syndrome --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:facial clefting syndrome | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  398. en:hypospadias --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:hypospadias | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  399. en:intellectual disability --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:intellectual disability | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  400. en:interatrial septal defect --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:interatrial septal defect | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  401. en:interventricular septal defect --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:interventricular septal defect | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  402. en:iris coloboma with ptosis --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:iris coloboma with ptosis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  403. en:microtia --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:microtia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  404. en:minimal pigment type --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:minimal pigment type | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  405. en:myopia --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:myopia | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  406. en:polysyndactyly syndrome --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:polysyndactyly syndrome | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  407. en:secundum defect --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:secundum defect | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  408. en:sinus venosus defect --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:sinus venosus defect | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  409. en:surgical treatment of hydrocele --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:surgical treatment of hydrocele | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  410. en:unusual facies --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:unusual facies | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  411. en:water on the brain --- r_associated #0: 10 --> en:major congenital anomaly
    n1=en:water on the brain | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  412. encéphalocèle --- r_associated #0: 10 --> en:major congenital anomaly
    n1=encéphalocèle | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  413. faciale (paralysie du nouveau-né) --- r_associated #0: 10 --> en:major congenital anomaly
    n1=faciale (paralysie du nouveau-né) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  414. fente nasolabiopalatine --- r_associated #0: 10 --> en:major congenital anomaly
    n1=fente nasolabiopalatine | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  415. gastroschisis --- r_associated #0: 10 --> en:major congenital anomaly
    n1=gastroschisis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  416. hernie diaphragmatique --- r_associated #0: 10 --> en:major congenital anomaly
    n1=hernie diaphragmatique | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  417. hydrocephalus --- r_associated #0: 10 --> en:major congenital anomaly
    n1=hydrocephalus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  418. hypertensinase --- r_associated #0: 10 --> en:major congenital anomaly
    n1=hypertensinase | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  419. hypertensine --- r_associated #0: 10 --> en:major congenital anomaly
    n1=hypertensine | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  420. hypertensinogène --- r_associated #0: 10 --> en:major congenital anomaly
    n1=hypertensinogène | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  421. hypertension --- r_associated #0: 10 --> en:major congenital anomaly
    n1=hypertension | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  422. hypertension abdominale --- r_associated #0: 10 --> en:major congenital anomaly
    n1=hypertension abdominale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  423. hypertension artérielle --- r_associated #0: 10 --> en:major congenital anomaly
    n1=hypertension artérielle | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  424. hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental --- r_associated #0: 10 --> en:major congenital anomaly
    n1=hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  425. hypohypophysie --- r_associated #0: 10 --> en:major congenital anomaly
    n1=hypohypophysie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  426. hypostimulinie --- r_associated #0: 10 --> en:major congenital anomaly
    n1=hypostimulinie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  427. impédance acoustique (symb. Z) --- r_associated #0: 10 --> en:major congenital anomaly
    n1=impédance acoustique (symb. Z) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  428. myéloméningocèle --- r_associated #0: 10 --> en:major congenital anomaly
    n1=myéloméningocèle | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  429. nanisme --- r_associated #0: 10 --> en:major congenital anomaly
    n1=nanisme | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  430. nystagmus --- r_associated #0: 10 --> en:major congenital anomaly
    n1=nystagmus | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  431. nystagmus héréditaire vertical --- r_associated #0: 10 --> en:major congenital anomaly
    n1=nystagmus héréditaire vertical | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  432. nystagmus lié au sexe --- r_associated #0: 10 --> en:major congenital anomaly
    n1=nystagmus lié au sexe | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  433. nystagmus myoclonies --- r_associated #0: 10 --> en:major congenital anomaly
    n1=nystagmus myoclonies | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  434. omovertébral (os) --- r_associated #0: 10 --> en:major congenital anomaly
    n1=omovertébral (os) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  435. quadriplégie spastique, rétinite pigmentaire et retard mental --- r_associated #0: 10 --> en:major congenital anomaly
    n1=quadriplégie spastique, rétinite pigmentaire et retard mental | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  436. rétinite pigmentaire et retard mental --- r_associated #0: 10 --> en:major congenital anomaly
    n1=rétinite pigmentaire et retard mental | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  437. rétinite pigmentaire, surdité, retard mental, et hypogonadisme --- r_associated #0: 10 --> en:major congenital anomaly
    n1=rétinite pigmentaire, surdité, retard mental, et hypogonadisme | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  438. spina bifida --- r_associated #0: 10 --> en:major congenital anomaly
    n1=spina bifida | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  439. surdité --- r_associated #0: 10 --> en:major congenital anomaly
    n1=surdité | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  440. syndrome cataracte-ataxie-surdité et retard mental --- r_associated #0: 10 --> en:major congenital anomaly
    n1=syndrome cataracte-ataxie-surdité et retard mental | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  441. syndrome de Treft-Sanborn-Carey --- r_associated #0: 10 --> en:major congenital anomaly
    n1=syndrome de Treft-Sanborn-Carey | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  442. trichomégalie avec retard mental, nanisme, et dégénérescence pigmentée de la rétine --- r_associated #0: 10 --> en:major congenital anomaly
    n1=trichomégalie avec retard mental, nanisme, et dégénérescence pigmentée de la rétine | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  443. télécardiographie --- r_associated #0: 10 --> en:major congenital anomaly
    n1=télécardiographie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  444. télécardiophone --- r_associated #0: 10 --> en:major congenital anomaly
    n1=télécardiophone | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  445. téléclitoridie --- r_associated #0: 10 --> en:major congenital anomaly
    n1=téléclitoridie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  446. télécobalt --- r_associated #0: 10 --> en:major congenital anomaly
    n1=télécobalt | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  447. télécobalt-thérapie --- r_associated #0: 10 --> en:major congenital anomaly
    n1=télécobalt-thérapie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  448. téléconsultation --- r_associated #0: 10 --> en:major congenital anomaly
    n1=téléconsultation | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  449. télécrâne --- r_associated #0: 10 --> en:major congenital anomaly
    n1=télécrâne | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  450. télécæsiothérapie --- r_associated #0: 10 --> en:major congenital anomaly
    n1=télécæsiothérapie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  451. télédermatologie --- r_associated #0: 10 --> en:major congenital anomaly
    n1=télédermatologie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  452. télédiastole --- r_associated #0: 10 --> en:major congenital anomaly
    n1=télédiastole | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  453. télédétection --- r_associated #0: 10 --> en:major congenital anomaly
    n1=télédétection | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  454. urticaire-surdité-amylose rénale --- r_associated #0: 10 --> en:major congenital anomaly
    n1=urticaire-surdité-amylose rénale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  455. uréosecrétoire (constante) --- r_associated #0: 10 --> en:major congenital anomaly
    n1=uréosecrétoire (constante) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=10
  456. ANKRD11 gene --- r_associated #0: 5 --> en:major congenital anomaly
    n1=ANKRD11 gene | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  457. ARRX --- r_associated #0: 5 --> en:major congenital anomaly
    n1=ARRX | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  458. Déficience mentale --- r_associated #0: 5 --> en:major congenital anomaly
    n1=Déficience mentale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  459. Exomphale --- r_associated #0: 5 --> en:major congenital anomaly
    n1=Exomphale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  460. Handicap mental --- r_associated #0: 5 --> en:major congenital anomaly
    n1=Handicap mental | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  461. albinisme avec immunodéficience et troubles hématologiques --- r_associated #0: 5 --> en:major congenital anomaly
    n1=albinisme avec immunodéficience et troubles hématologiques | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  462. albinisme avec surdité --- r_associated #0: 5 --> en:major congenital anomaly
    n1=albinisme avec surdité | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  463. ankyloblépharon --- r_associated #0: 5 --> en:major congenital anomaly
    n1=ankyloblépharon | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  464. ankyloblépharon filiforme et fente palatine --- r_associated #0: 5 --> en:major congenital anomaly
    n1=ankyloblépharon filiforme et fente palatine | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  465. ankyloblépharon, ongles hypoplasiques et cheveux bouclés --- r_associated #0: 5 --> en:major congenital anomaly
    n1=ankyloblépharon, ongles hypoplasiques et cheveux bouclés | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  466. ankyloblépharon-dysplasie ectodermique-fente labio-palatine --- r_associated #0: 5 --> en:major congenital anomaly
    n1=ankyloblépharon-dysplasie ectodermique-fente labio-palatine | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  467. arrière-pied --- r_associated #0: 5 --> en:major congenital anomaly
    n1=arrière-pied | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  468. cyclopeptide --- r_associated #0: 5 --> en:major congenital anomaly
    n1=cyclopeptide | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  469. cyclophiline --- r_associated #0: 5 --> en:major congenital anomaly
    n1=cyclophiline | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  470. cyclophorie --- r_associated #0: 5 --> en:major congenital anomaly
    n1=cyclophorie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  471. cyclophosphamide --- r_associated #0: 5 --> en:major congenital anomaly
    n1=cyclophosphamide | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  472. cyclophotocoagulation endoscopique --- r_associated #0: 5 --> en:major congenital anomaly
    n1=cyclophotocoagulation endoscopique | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  473. cyclophrénie --- r_associated #0: 5 --> en:major congenital anomaly
    n1=cyclophrénie | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  474. cyclophyllidés --- r_associated #0: 5 --> en:major congenital anomaly
    n1=cyclophyllidés | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  475. ellipse d'engagement --- r_associated #0: 5 --> en:major congenital anomaly
    n1=ellipse d'engagement | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  476. ellipt.ocytose --- r_associated #0: 5 --> en:major congenital anomaly
    n1=ellipt.ocytose | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  477. elliptocyte --- r_associated #0: 5 --> en:major congenital anomaly
    n1=elliptocyte | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  478. elliptocytose --- r_associated #0: 5 --> en:major congenital anomaly
    n1=elliptocytose | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  479. en:club-footed person --- r_associated #0: 5 --> en:major congenital anomaly
    n1=en:club-footed person | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  480. en:coronary disease --- r_associated #0: 5 --> en:major congenital anomaly
    n1=en:coronary disease | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  481. en:heart condition --- r_associated #0: 5 --> en:major congenital anomaly
    n1=en:heart condition | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  482. en:person with a club foot --- r_associated #0: 5 --> en:major congenital anomaly
    n1=en:person with a club foot | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  483. en:person with a clubfoot --- r_associated #0: 5 --> en:major congenital anomaly
    n1=en:person with a clubfoot | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  484. exencéphale --- r_associated #0: 5 --> en:major congenital anomaly
    n1=exencéphale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  485. exénatide --- r_associated #0: 5 --> en:major congenital anomaly
    n1=exénatide | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  486. hydrocèle de la femme --- r_associated #0: 5 --> en:major congenital anomaly
    n1=hydrocèle de la femme | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  487. hydrocèle de la vaginale --- r_associated #0: 5 --> en:major congenital anomaly
    n1=hydrocèle de la vaginale | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  488. hydrocèle du canal de Nück --- r_associated #0: 5 --> en:major congenital anomaly
    n1=hydrocèle du canal de Nück | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  489. hydrocèle du cou --- r_associated #0: 5 --> en:major congenital anomaly
    n1=hydrocèle du cou | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  490. laparoschisis --- r_associated #0: 5 --> en:major congenital anomaly
    n1=laparoschisis | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  491. nystagmus (zone de moindre) --- r_associated #0: 5 --> en:major congenital anomaly
    n1=nystagmus (zone de moindre) | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=5
  492. spina bifida --- r_associated #0: 5 --> en:major congenital anomaly
    n1=spina bifida | n2=en:major congenital anomaly | 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