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'en:dysmorphism'
(id=6906128 ; fe=en:dysmorphism ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=30180 creation date=2017-06-25 touchdate=2025-07-28 14:35:37.000)
≈ 334 relations sortantes

  1. en:dysmorphism -- r_associated #0: 42 / 1 -> en:connatal disorder
    n1=en:dysmorphism | n2=en:connatal disorder | rel=r_associated | relid=0 | w=42
  2. en:dysmorphism -- r_associated #0: 35 / 0.833 -> en:cleft palate
    n1=en:dysmorphism | n2=en:cleft palate | rel=r_associated | relid=0 | w=35
  3. en:dysmorphism -- r_associated #0: 35 / 0.833 -> en:congenital anomaly of central nervous system
    n1=en:dysmorphism | n2=en:congenital anomaly of central nervous system | rel=r_associated | relid=0 | w=35
  4. en:dysmorphism -- r_associated #0: 35 / 0.833 -> en:congenital nervous system disorder
    n1=en:dysmorphism | n2=en:congenital nervous system disorder | rel=r_associated | relid=0 | w=35
  5. en:dysmorphism -- r_associated #0: 34 / 0.81 -> en:congenital genitourinary abnormality
    n1=en:dysmorphism | n2=en:congenital genitourinary abnormality | rel=r_associated | relid=0 | w=34
  6. en:dysmorphism -- r_associated #0: 34 / 0.81 -> en:congenital malformation of face and neck, unspecified
    n1=en:dysmorphism | n2=en:congenital malformation of face and neck, unspecified | rel=r_associated | relid=0 | w=34
  7. en:dysmorphism -- r_associated #0: 32 / 0.762 -> dysmorphie
    n1=en:dysmorphism | n2=dysmorphie | rel=r_associated | relid=0 | w=32
  8. en:dysmorphism -- r_associated #0: 31 / 0.738 -> en:neurodevelopmental anomaly
    n1=en:dysmorphism | n2=en:neurodevelopmental anomaly | rel=r_associated | relid=0 | w=31
  9. en:dysmorphism -- r_associated #0: 30 / 0.714 -> en:congenital
    n1=en:dysmorphism | n2=en:congenital | rel=r_associated | relid=0 | w=30
  10. en:dysmorphism -- r_associated #0: 30 / 0.714 -> en:congenital morphologic anomaly
    n1=en:dysmorphism | n2=en:congenital morphologic anomaly | rel=r_associated | relid=0 | w=30
  11. en:dysmorphism -- r_associated #0: 30 / 0.714 -> en:congenital respiratory system disorder
    n1=en:dysmorphism | n2=en:congenital respiratory system disorder | rel=r_associated | relid=0 | w=30
  12. en:dysmorphism -- r_associated #0: 30 / 0.714 -> en:intestinal malrotation
    n1=en:dysmorphism | n2=en:intestinal malrotation | rel=r_associated | relid=0 | w=30
  13. en:dysmorphism -- r_associated #0: 30 / 0.714 -> en:oculo-dento-digital syndrome
    n1=en:dysmorphism | n2=en:oculo-dento-digital syndrome | rel=r_associated | relid=0 | w=30
  14. en:dysmorphism -- r_associated #0: 30 / 0.714 -> en:sirenomelia
    n1=en:dysmorphism | n2=en:sirenomelia | rel=r_associated | relid=0 | w=30
  15. en:dysmorphism -- r_associated #0: 29 / 0.69 -> en:anomaly congenital special senses
    n1=en:dysmorphism | n2=en:anomaly congenital special senses | rel=r_associated | relid=0 | w=29
  16. en:dysmorphism -- r_associated #0: 29 / 0.69 -> en:congenital eye disorder
    n1=en:dysmorphism | n2=en:congenital eye disorder | rel=r_associated | relid=0 | w=29
  17. en:dysmorphism -- r_associated #0: 29 / 0.69 -> en:heart malformation
    n1=en:dysmorphism | n2=en:heart malformation | rel=r_associated | relid=0 | w=29
  18. en:dysmorphism -- r_associated #0: 29 / 0.69 -> en:kbg syndrome
    n1=en:dysmorphism | n2=en:kbg syndrome | rel=r_associated | relid=0 | w=29
  19. en:dysmorphism -- r_associated #0: 29 / 0.69 -> en:persistent cloaca
    n1=en:dysmorphism | n2=en:persistent cloaca | rel=r_associated | relid=0 | w=29
  20. en:dysmorphism -- r_associated #0: 29 / 0.69 -> malformation cardiaque
    n1=en:dysmorphism | n2=malformation cardiaque | rel=r_associated | relid=0 | w=29
  21. en:dysmorphism -- r_associated #0: 28 / 0.667 -> en:amegakaryocytic thrombocytopenia with congenital malformation
    n1=en:dysmorphism | n2=en:amegakaryocytic thrombocytopenia with congenital malformation | rel=r_associated | relid=0 | w=28
  22. en:dysmorphism -- r_associated #0: 28 / 0.667 -> en:congenital anomaly of gastrointestinal tract
    n1=en:dysmorphism | n2=en:congenital anomaly of gastrointestinal tract | rel=r_associated | relid=0 | w=28
  23. en:dysmorphism -- r_associated #0: 28 / 0.667 -> en:congenital stenosis
    n1=en:dysmorphism | n2=en:congenital stenosis | rel=r_associated | relid=0 | w=28
  24. en:dysmorphism -- r_associated #0: 27 / 0.643 -> en:aicardi syndrome
    n1=en:dysmorphism | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=27
  25. en:dysmorphism -- r_associated #0: 27 / 0.643 -> en:atrial septal defect
    n1=en:dysmorphism | n2=en:atrial septal defect | rel=r_associated | relid=0 | w=27
  26. en:dysmorphism -- r_associated #0: 27 / 0.643 -> en:ellis-van creveld syndrome
    n1=en:dysmorphism | n2=en:ellis-van creveld syndrome | rel=r_associated | relid=0 | w=27
  27. en:dysmorphism -- r_associated #0: 27 / 0.643 -> en:fetal postural deformity
    n1=en:dysmorphism | n2=en:fetal postural deformity | rel=r_associated | relid=0 | w=27
  28. en:dysmorphism -- r_associated #0: 27 / 0.643 -> en:imperforate anus
    n1=en:dysmorphism | n2=en:imperforate anus | rel=r_associated | relid=0 | w=27
  29. en:dysmorphism -- r_associated #0: 27 / 0.643 -> en:other specified congenital malformations of face and neck
    n1=en:dysmorphism | n2=en:other specified congenital malformations of face and neck | rel=r_associated | relid=0 | w=27
  30. en:dysmorphism -- r_associated #0: 27 / 0.643 -> en:ventricular septal defect
    n1=en:dysmorphism | n2=en:ventricular septal defect | rel=r_associated | relid=0 | w=27
  31. en:dysmorphism -- r_associated #0: 26 / 0.619 -> en:arthrogryposis
    n1=en:dysmorphism | n2=en:arthrogryposis | rel=r_associated | relid=0 | w=26
  32. en:dysmorphism -- r_associated #0: 26 / 0.619 -> en:biliary atresia
    n1=en:dysmorphism | n2=en:biliary atresia | rel=r_associated | relid=0 | w=26
  33. en:dysmorphism -- r_associated #0: 26 / 0.619 -> en:classical phenylketonuria
    n1=en:dysmorphism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=26
  34. en:dysmorphism -- r_associated #0: 26 / 0.619 -> en:congenital abnormality
    n1=en:dysmorphism | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=26
  35. en:dysmorphism -- r_associated #0: 26 / 0.619 -> en:congenital abnormality of lower limb and/or pelvic girdle
    n1=en:dysmorphism | n2=en:congenital abnormality of lower limb and/or pelvic girdle | rel=r_associated | relid=0 | w=26
  36. en:dysmorphism -- r_associated #0: 26 / 0.619 -> en:congenital deformity of knee joint
    n1=en:dysmorphism | n2=en:congenital deformity of knee joint | rel=r_associated | relid=0 | w=26
  37. en:dysmorphism -- r_associated #0: 26 / 0.619 -> en:congenital musculoskeletal defect
    n1=en:dysmorphism | n2=en:congenital musculoskeletal defect | rel=r_associated | relid=0 | w=26
  38. en:dysmorphism -- r_associated #0: 26 / 0.619 -> en:congenital urinary system abnormality
    n1=en:dysmorphism | n2=en:congenital urinary system abnormality | rel=r_associated | relid=0 | w=26
  39. en:dysmorphism -- r_associated #0: 26 / 0.619 -> en:noonan syndrome
    n1=en:dysmorphism | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=26
  40. en:dysmorphism -- r_associated #0: 26 / 0.619 -> en:phaces syndrome
    n1=en:dysmorphism | n2=en:phaces syndrome | rel=r_associated | relid=0 | w=26
  41. en:dysmorphism -- r_associated #0: 25 / 0.595 -> en:cohen syndrome
    n1=en:dysmorphism | n2=en:cohen syndrome | rel=r_associated | relid=0 | w=25
  42. en:dysmorphism -- r_associated #0: 25 / 0.595 -> en:hypertrophy of clitoris
    n1=en:dysmorphism | n2=en:hypertrophy of clitoris | rel=r_associated | relid=0 | w=25
  43. en:dysmorphism -- r_associated #0: 25 / 0.595 -> en:neural tube defect
    n1=en:dysmorphism | n2=en:neural tube defect | rel=r_associated | relid=0 | w=25
  44. en:dysmorphism -- r_associated #0: 25 / 0.595 -> en:sotos syndrome
    n1=en:dysmorphism | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=25
  45. en:dysmorphism -- r_associated #0: 25 / 0.595 -> en:thoracoschisis
    n1=en:dysmorphism | n2=en:thoracoschisis | rel=r_associated | relid=0 | w=25
  46. en:dysmorphism -- r_associated #0: 24 / 0.571 -> en:chromosome disorder
    n1=en:dysmorphism | n2=en:chromosome disorder | rel=r_associated | relid=0 | w=24
  47. en:dysmorphism -- r_associated #0: 24 / 0.571 -> en:congenital anomaly of joint
    n1=en:dysmorphism | n2=en:congenital anomaly of joint | rel=r_associated | relid=0 | w=24
  48. en:dysmorphism -- r_associated #0: 24 / 0.571 -> en:congenital deformity of hip
    n1=en:dysmorphism | n2=en:congenital deformity of hip | rel=r_associated | relid=0 | w=24
  49. en:dysmorphism -- r_associated #0: 24 / 0.571 -> en:musculoskeletal disorders congenital nec
    n1=en:dysmorphism | n2=en:musculoskeletal disorders congenital nec | rel=r_associated | relid=0 | w=24
  50. en:dysmorphism -- r_associated #0: 23 / 0.548 -> anomalie congénitale
    n1=en:dysmorphism | n2=anomalie congénitale | rel=r_associated | relid=0 | w=23
  51. en:dysmorphism -- r_associated #0: 23 / 0.548 -> en:bowen-conradi syndrome
    n1=en:dysmorphism | n2=en:bowen-conradi syndrome | rel=r_associated | relid=0 | w=23
  52. en:dysmorphism -- r_associated #0: 23 / 0.548 -> en:cardiovascular abnormalities
    n1=en:dysmorphism | n2=en:cardiovascular abnormalities | rel=r_associated | relid=0 | w=23
  53. en:dysmorphism -- r_associated #0: 23 / 0.548 -> en:laron syndrome
    n1=en:dysmorphism | n2=en:laron syndrome | rel=r_associated | relid=0 | w=23
  54. en:dysmorphism -- r_associated #0: 23 / 0.548 -> en:lowry wood syndrome
    n1=en:dysmorphism | n2=en:lowry wood syndrome | rel=r_associated | relid=0 | w=23
  55. en:dysmorphism -- r_associated #0: 23 / 0.548 -> en:mental retardation
    n1=en:dysmorphism | n2=en:mental retardation | rel=r_associated | relid=0 | w=23
  56. en:dysmorphism -- r_associated #0: 22 / 0.524 -> en:congenital dysplasia
    n1=en:dysmorphism | n2=en:congenital dysplasia | rel=r_associated | relid=0 | w=22
  57. en:dysmorphism -- r_associated #0: 22 / 0.524 -> en:congenital hypoplasia of genital tubercle
    n1=en:dysmorphism | n2=en:congenital hypoplasia of genital tubercle | rel=r_associated | relid=0 | w=22
  58. en:dysmorphism -- r_associated #0: 22 / 0.524 -> en:nail-patella syndrome
    n1=en:dysmorphism | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=22
  59. en:dysmorphism -- r_associated #0: 22 / 0.524 -> en:nicolaides baraitser syndrome
    n1=en:dysmorphism | n2=en:nicolaides baraitser syndrome | rel=r_associated | relid=0 | w=22
  60. en:dysmorphism -- r_associated #0: 22 / 0.524 -> en:precocious puberty
    n1=en:dysmorphism | n2=en:precocious puberty | rel=r_associated | relid=0 | w=22
  61. en:dysmorphism -- r_associated #0: 22 / 0.524 -> en:transposition of great vessels
    n1=en:dysmorphism | n2=en:transposition of great vessels | rel=r_associated | relid=0 | w=22
  62. en:dysmorphism -- r_associated #0: 21 / 0.5 -> en:aase syndrome
    n1=en:dysmorphism | n2=en:aase syndrome | rel=r_associated | relid=0 | w=21
  63. en:dysmorphism -- r_associated #0: 21 / 0.5 -> en:congenital foot deformity
    n1=en:dysmorphism | n2=en:congenital foot deformity | rel=r_associated | relid=0 | w=21
  64. en:dysmorphism -- r_associated #0: 21 / 0.5 -> en:ectodermal dysplasia
    n1=en:dysmorphism | n2=en:ectodermal dysplasia | rel=r_associated | relid=0 | w=21
  65. en:dysmorphism -- r_associated #0: 21 / 0.5 -> en:kabuki syndrome
    n1=en:dysmorphism | n2=en:kabuki syndrome | rel=r_associated | relid=0 | w=21
  66. en:dysmorphism -- r_associated #0: 21 / 0.5 -> en:syndrome, mohr
    n1=en:dysmorphism | n2=en:syndrome, mohr | rel=r_associated | relid=0 | w=21
  67. en:dysmorphism -- r_associated #0: 20 / 0.476 -> affection cardiaque
    n1=en:dysmorphism | n2=affection cardiaque | rel=r_associated | relid=0 | w=20
  68. en:dysmorphism -- r_associated #0: 20 / 0.476 -> affection oculaire congénitale
    n1=en:dysmorphism | n2=affection oculaire congénitale | rel=r_associated | relid=0 | w=20
  69. en:dysmorphism -- r_associated #0: 20 / 0.476 -> affections cardiaques
    n1=en:dysmorphism | n2=affections cardiaques | rel=r_associated | relid=0 | w=20
  70. en:dysmorphism -- r_associated #0: 20 / 0.476 -> albinisme
    n1=en:dysmorphism | n2=albinisme | rel=r_associated | relid=0 | w=20
  71. en:dysmorphism -- r_associated #0: 20 / 0.476 -> albinisme oculocutané de type mutant jaune
    n1=en:dysmorphism | n2=albinisme oculocutané de type mutant jaune | rel=r_associated | relid=0 | w=20
  72. en:dysmorphism -- r_associated #0: 20 / 0.476 -> ancyloglosse
    n1=en:dysmorphism | n2=ancyloglosse | rel=r_associated | relid=0 | w=20
  73. en:dysmorphism -- r_associated #0: 20 / 0.476 -> ankyloglosse
    n1=en:dysmorphism | n2=ankyloglosse | rel=r_associated | relid=0 | w=20
  74. en:dysmorphism -- r_associated #0: 20 / 0.476 -> anomalie cardiaque
    n1=en:dysmorphism | n2=anomalie cardiaque | rel=r_associated | relid=0 | w=20
  75. en:dysmorphism -- r_associated #0: 20 / 0.476 -> anomalie chromosomique
    n1=en:dysmorphism | n2=anomalie chromosomique | rel=r_associated | relid=0 | w=20
  76. en:dysmorphism -- r_associated #0: 20 / 0.476 -> anomalie congénitale de l'oeil
    n1=en:dysmorphism | n2=anomalie congénitale de l'oeil | rel=r_associated | relid=0 | w=20
  77. en:dysmorphism -- r_associated #0: 20 / 0.476 -> anomalie cytogénétique
    n1=en:dysmorphism | n2=anomalie cytogénétique | rel=r_associated | relid=0 | w=20
  78. en:dysmorphism -- r_associated #0: 20 / 0.476 -> anomalie du coeur
    n1=en:dysmorphism | n2=anomalie du coeur | rel=r_associated | relid=0 | w=20
  79. en:dysmorphism -- r_associated #0: 20 / 0.476 -> anomalie du développement
    n1=en:dysmorphism | n2=anomalie du développement | rel=r_associated | relid=0 | w=20
  80. en:dysmorphism -- r_associated #0: 20 / 0.476 -> anomalie du septum auriculaire
    n1=en:dysmorphism | n2=anomalie du septum auriculaire | rel=r_associated | relid=0 | w=20
  81. en:dysmorphism -- r_associated #0: 20 / 0.476 -> anormalité des chromosomes
    n1=en:dysmorphism | n2=anormalité des chromosomes | rel=r_associated | relid=0 | w=20
  82. en:dysmorphism -- r_associated #0: 20 / 0.476 -> arriération
    n1=en:dysmorphism | n2=arriération | rel=r_associated | relid=0 | w=20
  83. en:dysmorphism -- r_associated #0: 20 / 0.476 -> arriération mentale
    n1=en:dysmorphism | n2=arriération mentale | rel=r_associated | relid=0 | w=20
  84. en:dysmorphism -- r_associated #0: 20 / 0.476 -> arthrogrypose
    n1=en:dysmorphism | n2=arthrogrypose | rel=r_associated | relid=0 | w=20
  85. en:dysmorphism -- r_associated #0: 20 / 0.476 -> brides amniotiques (syndrome des)
    n1=en:dysmorphism | n2=brides amniotiques (syndrome des) | rel=r_associated | relid=0 | w=20
  86. en:dysmorphism -- r_associated #0: 20 / 0.476 -> card
    n1=en:dysmorphism | n2=card | rel=r_associated | relid=0 | w=20
  87. en:dysmorphism -- r_associated #0: 20 / 0.476 -> cardiopathie
    n1=en:dysmorphism | n2=cardiopathie | rel=r_associated | relid=0 | w=20
  88. en:dysmorphism -- r_associated #0: 20 / 0.476 -> cardiopathies
    n1=en:dysmorphism | n2=cardiopathies | rel=r_associated | relid=0 | w=20
  89. en:dysmorphism -- r_associated #0: 20 / 0.476 -> cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie
    n1=en:dysmorphism | n2=cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie | rel=r_associated | relid=0 | w=20
  90. en:dysmorphism -- r_associated #0: 20 / 0.476 -> colobome de l'iris avec ptosis, hypertélorisme et retard mental
    n1=en:dysmorphism | n2=colobome de l'iris avec ptosis, hypertélorisme et retard mental | rel=r_associated | relid=0 | w=20
  91. en:dysmorphism -- r_associated #0: 20 / 0.476 -> communication interauriculaire
    n1=en:dysmorphism | n2=communication interauriculaire | rel=r_associated | relid=0 | w=20
  92. en:dysmorphism -- r_associated #0: 20 / 0.476 -> congénital
    n1=en:dysmorphism | n2=congénital | rel=r_associated | relid=0 | w=20
  93. en:dysmorphism -- r_associated #0: 20 / 0.476 -> congenital
    n1=en:dysmorphism | n2=congenital | rel=r_associated | relid=0 | w=20
  94. en:dysmorphism -- r_associated #0: 20 / 0.476 -> congénitale
    n1=en:dysmorphism | n2=congénitale | rel=r_associated | relid=0 | w=20
  95. en:dysmorphism -- r_associated #0: 20 / 0.476 -> contractures congénitales et arachnodactylie
    n1=en:dysmorphism | n2=contractures congénitales et arachnodactylie | rel=r_associated | relid=0 | w=20
  96. en:dysmorphism -- r_associated #0: 20 / 0.476 -> crânio-sténose
    n1=en:dysmorphism | n2=crânio-sténose | rel=r_associated | relid=0 | w=20
  97. en:dysmorphism -- r_associated #0: 20 / 0.476 -> craniosténose
    n1=en:dysmorphism | n2=craniosténose | rel=r_associated | relid=0 | w=20
  98. en:dysmorphism -- r_associated #0: 20 / 0.476 -> crâniosténose
    n1=en:dysmorphism | n2=crâniosténose | rel=r_associated | relid=0 | w=20
  99. en:dysmorphism -- r_associated #0: 20 / 0.476 -> craniosynostose
    n1=en:dysmorphism | n2=craniosynostose | rel=r_associated | relid=0 | w=20
  100. en:dysmorphism -- r_associated #0: 20 / 0.476 -> crâniosynostose
    n1=en:dysmorphism | n2=crâniosynostose | rel=r_associated | relid=0 | w=20
  101. en:dysmorphism -- r_associated #0: 20 / 0.476 -> cyclopia
    n1=en:dysmorphism | n2=cyclopia | rel=r_associated | relid=0 | w=20
  102. en:dysmorphism -- r_associated #0: 20 / 0.476 -> cyclopie
    n1=en:dysmorphism | n2=cyclopie | rel=r_associated | relid=0 | w=20
  103. en:dysmorphism -- r_associated #0: 20 / 0.476 -> débilité mentale
    n1=en:dysmorphism | n2=débilité mentale | rel=r_associated | relid=0 | w=20
  104. en:dysmorphism -- r_associated #0: 20 / 0.476 -> déficience congénitale
    n1=en:dysmorphism | n2=déficience congénitale | rel=r_associated | relid=0 | w=20
  105. en:dysmorphism -- r_associated #0: 20 / 0.476 -> déficience intellectuelle
    n1=en:dysmorphism | n2=déficience intellectuelle | rel=r_associated | relid=0 | w=20
  106. en:dysmorphism -- r_associated #0: 20 / 0.476 -> déficience mentale
    n1=en:dysmorphism | n2=déficience mentale | rel=r_associated | relid=0 | w=20
  107. en:dysmorphism -- r_associated #0: 20 / 0.476 -> déformation congénitale
    n1=en:dysmorphism | n2=déformation congénitale | rel=r_associated | relid=0 | w=20
  108. en:dysmorphism -- r_associated #0: 20 / 0.476 -> difformité congénitale
    n1=en:dysmorphism | n2=difformité congénitale | rel=r_associated | relid=0 | w=20
  109. en:dysmorphism -- r_associated #0: 20 / 0.476 -> dysplasie ectodermique
    n1=en:dysmorphism | n2=dysplasie ectodermique | rel=r_associated | relid=0 | w=20
  110. en:dysmorphism -- r_associated #0: 20 / 0.476 -> dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental
    n1=en:dysmorphism | n2=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | rel=r_associated | relid=0 | w=20
  111. en:dysmorphism -- r_associated #0: 20 / 0.476 -> dysplasie ectodermique, ectrodactylie et dystrophie maculaire
    n1=en:dysmorphism | n2=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | rel=r_associated | relid=0 | w=20
  112. en:dysmorphism -- r_associated #0: 20 / 0.476 -> ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie)
    n1=en:dysmorphism | n2=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | rel=r_associated | relid=0 | w=20
  113. en:dysmorphism -- r_associated #0: 20 / 0.476 -> ectopia cordis
    n1=en:dysmorphism | n2=ectopia cordis | rel=r_associated | relid=0 | w=20
  114. en:dysmorphism -- r_associated #0: 20 / 0.476 -> ectopie cardiaque
    n1=en:dysmorphism | n2=ectopie cardiaque | rel=r_associated | relid=0 | w=20
  115. en:dysmorphism -- r_associated #0: 20 / 0.476 -> elliptocytose héréditaire
    n1=en:dysmorphism | n2=elliptocytose héréditaire | rel=r_associated | relid=0 | w=20
  116. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:abnormalities, drug-induced
    n1=en:dysmorphism | n2=en:abnormalities, drug-induced | rel=r_associated | relid=0 | w=20
  117. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:abnormality, severe teratoid
    n1=en:dysmorphism | n2=en:abnormality, severe teratoid | rel=r_associated | relid=0 | w=20
  118. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:absent corpus callosum
    n1=en:dysmorphism | n2=en:absent corpus callosum | rel=r_associated | relid=0 | w=20
  119. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:adrenal cytomegaly
    n1=en:dysmorphism | n2=en:adrenal cytomegaly | rel=r_associated | relid=0 | w=20
  120. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:albinism
    n1=en:dysmorphism | n2=en:albinism | rel=r_associated | relid=0 | w=20
  121. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:amniotic band syndrome
    n1=en:dysmorphism | n2=en:amniotic band syndrome | rel=r_associated | relid=0 | w=20
  122. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:anal imperforation
    n1=en:dysmorphism | n2=en:anal imperforation | rel=r_associated | relid=0 | w=20
  123. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:and mental retardation
    n1=en:dysmorphism | n2=en:and mental retardation | rel=r_associated | relid=0 | w=20
  124. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:ankyloglossia
    n1=en:dysmorphism | n2=en:ankyloglossia | rel=r_associated | relid=0 | w=20
  125. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:aplasia, nos
    n1=en:dysmorphism | n2=en:aplasia, nos | rel=r_associated | relid=0 | w=20
  126. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:birth defect
    n1=en:dysmorphism | n2=en:birth defect | rel=r_associated | relid=0 | w=20
  127. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:card
    n1=en:dysmorphism | n2=en:card | rel=r_associated | relid=0 | w=20
  128. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:cardiac diseases
    n1=en:dysmorphism | n2=en:cardiac diseases | rel=r_associated | relid=0 | w=20
  129. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:caroli disease
    n1=en:dysmorphism | n2=en:caroli disease | rel=r_associated | relid=0 | w=20
  130. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:caudal dysplasia
    n1=en:dysmorphism | n2=en:caudal dysplasia | rel=r_associated | relid=0 | w=20
  131. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:celosomy
    n1=en:dysmorphism | n2=en:celosomy | rel=r_associated | relid=0 | w=20
  132. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:cerebellar atrophy
    n1=en:dysmorphism | n2=en:cerebellar atrophy | rel=r_associated | relid=0 | w=20
  133. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:cerebral gigantism
    n1=en:dysmorphism | n2=en:cerebral gigantism | rel=r_associated | relid=0 | w=20
  134. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:cerebral ventriculomegaly
    n1=en:dysmorphism | n2=en:cerebral ventriculomegaly | rel=r_associated | relid=0 | w=20
  135. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:certain congenital musculoskeletal deformities
    n1=en:dysmorphism | n2=en:certain congenital musculoskeletal deformities | rel=r_associated | relid=0 | w=20
  136. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:chromosomal aberration
    n1=en:dysmorphism | n2=en:chromosomal aberration | rel=r_associated | relid=0 | w=20
  137. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:chromosomal abnormality
    n1=en:dysmorphism | n2=en:chromosomal abnormality | rel=r_associated | relid=0 | w=20
  138. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:cleft lip and palate
    n1=en:dysmorphism | n2=en:cleft lip and palate | rel=r_associated | relid=0 | w=20
  139. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:cleft maxilla
    n1=en:dysmorphism | n2=en:cleft maxilla | rel=r_associated | relid=0 | w=20
  140. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:cleft palate with cleft lip
    n1=en:dysmorphism | n2=en:cleft palate with cleft lip | rel=r_associated | relid=0 | w=20
  141. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital abnormal fusion
    n1=en:dysmorphism | n2=en:congenital abnormal fusion | rel=r_associated | relid=0 | w=20
  142. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital anomaly
    n1=en:dysmorphism | n2=en:congenital anomaly | rel=r_associated | relid=0 | w=20
  143. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital anomaly of face
    n1=en:dysmorphism | n2=en:congenital anomaly of face | rel=r_associated | relid=0 | w=20
  144. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital cardiovascular abnormality
    n1=en:dysmorphism | n2=en:congenital cardiovascular abnormality | rel=r_associated | relid=0 | w=20
  145. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital defect
    n1=en:dysmorphism | n2=en:congenital defect | rel=r_associated | relid=0 | w=20
  146. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital enlargement
    n1=en:dysmorphism | n2=en:congenital enlargement | rel=r_associated | relid=0 | w=20
  147. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital extension deformity
    n1=en:dysmorphism | n2=en:congenital extension deformity | rel=r_associated | relid=0 | w=20
  148. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital failure of fusion
    n1=en:dysmorphism | n2=en:congenital failure of fusion | rel=r_associated | relid=0 | w=20
  149. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital keratoglobus
    n1=en:dysmorphism | n2=en:congenital keratoglobus | rel=r_associated | relid=0 | w=20
  150. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital macrocephaly
    n1=en:dysmorphism | n2=en:congenital macrocephaly | rel=r_associated | relid=0 | w=20
  151. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital malformation
    n1=en:dysmorphism | n2=en:congenital malformation | rel=r_associated | relid=0 | w=20
  152. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital malformation syndrome
    n1=en:dysmorphism | n2=en:congenital malformation syndrome | rel=r_associated | relid=0 | w=20
  153. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital malformation syndrome related to known exogenous cause
    n1=en:dysmorphism | n2=en:congenital malformation syndrome related to known exogenous cause | rel=r_associated | relid=0 | w=20
  154. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital septation
    n1=en:dysmorphism | n2=en:congenital septation | rel=r_associated | relid=0 | w=20
  155. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital systemic disorder
    n1=en:dysmorphism | n2=en:congenital systemic disorder | rel=r_associated | relid=0 | w=20
  156. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:congenital vena cava abnormality
    n1=en:dysmorphism | n2=en:congenital vena cava abnormality | rel=r_associated | relid=0 | w=20
  157. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:conjoined twins
    n1=en:dysmorphism | n2=en:conjoined twins | rel=r_associated | relid=0 | w=20
  158. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:costello syndrome
    n1=en:dysmorphism | n2=en:costello syndrome | rel=r_associated | relid=0 | w=20
  159. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:cranioschisis
    n1=en:dysmorphism | n2=en:cranioschisis | rel=r_associated | relid=0 | w=20
  160. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:craniosynostosis
    n1=en:dysmorphism | n2=en:craniosynostosis | rel=r_associated | relid=0 | w=20
  161. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:cryptophthalmia
    n1=en:dysmorphism | n2=en:cryptophthalmia | rel=r_associated | relid=0 | w=20
  162. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:cyclopia
    n1=en:dysmorphism | n2=en:cyclopia | rel=r_associated | relid=0 | w=20
  163. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:delayed epiphyseal fusion
    n1=en:dysmorphism | n2=en:delayed epiphyseal fusion | rel=r_associated | relid=0 | w=20
  164. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:developmental anomaly
    n1=en:dysmorphism | n2=en:developmental anomaly | rel=r_associated | relid=0 | w=20
  165. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:developmental fault
    n1=en:dysmorphism | n2=en:developmental fault | rel=r_associated | relid=0 | w=20
  166. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:developmental immaturity
    n1=en:dysmorphism | n2=en:developmental immaturity | rel=r_associated | relid=0 | w=20
  167. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:ear, face and neck congenital anomalies
    n1=en:dysmorphism | n2=en:ear, face and neck congenital anomalies | rel=r_associated | relid=0 | w=20
  168. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:ectopia cordis
    n1=en:dysmorphism | n2=en:ectopia cordis | rel=r_associated | relid=0 | w=20
  169. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:embryonic cyst
    n1=en:dysmorphism | n2=en:embryonic cyst | rel=r_associated | relid=0 | w=20
  170. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:epiphyseal dysplasia dysmorphism camptodactyly
    n1=en:dysmorphism | n2=en:epiphyseal dysplasia dysmorphism camptodactyly | rel=r_associated | relid=0 | w=20
  171. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:epiphyseal dysplasia hearing loss dysmorphism
    n1=en:dysmorphism | n2=en:epiphyseal dysplasia hearing loss dysmorphism | rel=r_associated | relid=0 | w=20
  172. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:ethmocephaly
    n1=en:dysmorphism | n2=en:ethmocephaly | rel=r_associated | relid=0 | w=20
  173. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:exencephaly
    n1=en:dysmorphism | n2=en:exencephaly | rel=r_associated | relid=0 | w=20
  174. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:exenkephaly
    n1=en:dysmorphism | n2=en:exenkephaly | rel=r_associated | relid=0 | w=20
  175. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:exomphalos
    n1=en:dysmorphism | n2=en:exomphalos | rel=r_associated | relid=0 | w=20
  176. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:exstrophy
    n1=en:dysmorphism | n2=en:exstrophy | rel=r_associated | relid=0 | w=20
  177. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:exumbilication
    n1=en:dysmorphism | n2=en:exumbilication | rel=r_associated | relid=0 | w=20
  178. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:facial cleft
    n1=en:dysmorphism | n2=en:facial cleft | rel=r_associated | relid=0 | w=20
  179. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:faciodigitogenital dysplasia
    n1=en:dysmorphism | n2=en:faciodigitogenital dysplasia | rel=r_associated | relid=0 | w=20
  180. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:failure of the mind
    n1=en:dysmorphism | n2=en:failure of the mind | rel=r_associated | relid=0 | w=20
  181. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:Fallot's disease
    n1=en:dysmorphism | n2=en:Fallot's disease | rel=r_associated | relid=0 | w=20
  182. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:gigantism and hyperplastic visceromegaly
    n1=en:dysmorphism | n2=en:gigantism and hyperplastic visceromegaly | rel=r_associated | relid=0 | w=20
  183. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:hand and foot deformity
    n1=en:dysmorphism | n2=en:hand and foot deformity | rel=r_associated | relid=0 | w=20
  184. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:heart disease
    n1=en:dysmorphism | n2=en:heart disease | rel=r_associated | relid=0 | w=20
  185. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:heart diseases
    n1=en:dysmorphism | n2=en:heart diseases | rel=r_associated | relid=0 | w=20
  186. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:heart disorder
    n1=en:dysmorphism | n2=en:heart disorder | rel=r_associated | relid=0 | w=20
  187. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:hematomphalus
    n1=en:dysmorphism | n2=en:hematomphalus | rel=r_associated | relid=0 | w=20
  188. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:hereditary elliptocytosis
    n1=en:dysmorphism | n2=en:hereditary elliptocytosis | rel=r_associated | relid=0 | w=20
  189. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:heterotaxy
    n1=en:dysmorphism | n2=en:heterotaxy | rel=r_associated | relid=0 | w=20
  190. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:heterotaxy syndrome
    n1=en:dysmorphism | n2=en:heterotaxy syndrome | rel=r_associated | relid=0 | w=20
  191. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:hydrencephalus
    n1=en:dysmorphism | n2=en:hydrencephalus | rel=r_associated | relid=0 | w=20
  192. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:hydrocephalus
    n1=en:dysmorphism | n2=en:hydrocephalus | rel=r_associated | relid=0 | w=20
  193. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:hypertelorism
    n1=en:dysmorphism | n2=en:hypertelorism | rel=r_associated | relid=0 | w=20
  194. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:hypopituitarism
    n1=en:dysmorphism | n2=en:hypopituitarism | rel=r_associated | relid=0 | w=20
  195. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:hypoplasia
    n1=en:dysmorphism | n2=en:hypoplasia | rel=r_associated | relid=0 | w=20
  196. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:hypothalamic hamartoblastoma
    n1=en:dysmorphism | n2=en:hypothalamic hamartoblastoma | rel=r_associated | relid=0 | w=20
  197. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:infantile fibrosarcoma
    n1=en:dysmorphism | n2=en:infantile fibrosarcoma | rel=r_associated | relid=0 | w=20
  198. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:infection causing congenital anomaly
    n1=en:dysmorphism | n2=en:infection causing congenital anomaly | rel=r_associated | relid=0 | w=20
  199. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:known or suspected fetal abnormality affecting management of mother
    n1=en:dysmorphism | n2=en:known or suspected fetal abnormality affecting management of mother | rel=r_associated | relid=0 | w=20
  200. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:kosaki overgrowth syndrome
    n1=en:dysmorphism | n2=en:kosaki overgrowth syndrome | rel=r_associated | relid=0 | w=20
  201. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:learning disability
    n1=en:dysmorphism | n2=en:learning disability | rel=r_associated | relid=0 | w=20
  202. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:limb deformities, congenital
    n1=en:dysmorphism | n2=en:limb deformities, congenital | rel=r_associated | relid=0 | w=20
  203. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:lymphatic abnormalities
    n1=en:dysmorphism | n2=en:lymphatic abnormalities | rel=r_associated | relid=0 | w=20
  204. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:macroglossia
    n1=en:dysmorphism | n2=en:macroglossia | rel=r_associated | relid=0 | w=20
  205. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:major physical defect
    n1=en:dysmorphism | n2=en:major physical defect | rel=r_associated | relid=0 | w=20
  206. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:megaloglossia
    n1=en:dysmorphism | n2=en:megaloglossia | rel=r_associated | relid=0 | w=20
  207. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:mental deficiency
    n1=en:dysmorphism | n2=en:mental deficiency | rel=r_associated | relid=0 | w=20
  208. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:mental handicap
    n1=en:dysmorphism | n2=en:mental handicap | rel=r_associated | relid=0 | w=20
  209. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:monster (disorder)
    n1=en:dysmorphism | n2=en:monster (disorder) | rel=r_associated | relid=0 | w=20
  210. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:nystagmus
    n1=en:dysmorphism | n2=en:nystagmus | rel=r_associated | relid=0 | w=20
  211. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:oligergasia
    n1=en:dysmorphism | n2=en:oligergasia | rel=r_associated | relid=0 | w=20
  212. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:oligophrenia
    n1=en:dysmorphism | n2=en:oligophrenia | rel=r_associated | relid=0 | w=20
  213. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:oligopsychia
    n1=en:dysmorphism | n2=en:oligopsychia | rel=r_associated | relid=0 | w=20
  214. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:ombilical hernia
    n1=en:dysmorphism | n2=en:ombilical hernia | rel=r_associated | relid=0 | w=20
  215. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:omphalocele
    n1=en:dysmorphism | n2=en:omphalocele | rel=r_associated | relid=0 | w=20
  216. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:other and unspecified congenital anomalies
    n1=en:dysmorphism | n2=en:other and unspecified congenital anomalies | rel=r_associated | relid=0 | w=20
  217. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:other congenital anomalies of nervous system
    n1=en:dysmorphism | n2=en:other congenital anomalies of nervous system | rel=r_associated | relid=0 | w=20
  218. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:other congenital malformations of digestive system
    n1=en:dysmorphism | n2=en:other congenital malformations of digestive system | rel=r_associated | relid=0 | w=20
  219. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:other specified congenital malformations
    n1=en:dysmorphism | n2=en:other specified congenital malformations | rel=r_associated | relid=0 | w=20
  220. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:otocephaly
    n1=en:dysmorphism | n2=en:otocephaly | rel=r_associated | relid=0 | w=20
  221. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:physical defect
    n1=en:dysmorphism | n2=en:physical defect | rel=r_associated | relid=0 | w=20
  222. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:proctatresia
    n1=en:dysmorphism | n2=en:proctatresia | rel=r_associated | relid=0 | w=20
  223. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:pyloric obstruction
    n1=en:dysmorphism | n2=en:pyloric obstruction | rel=r_associated | relid=0 | w=20
  224. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:pyloric stenosis
    n1=en:dysmorphism | n2=en:pyloric stenosis | rel=r_associated | relid=0 | w=20
  225. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:radiation-induced disorder
    n1=en:dysmorphism | n2=en:radiation-induced disorder | rel=r_associated | relid=0 | w=20
  226. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:retardation
    n1=en:dysmorphism | n2=en:retardation | rel=r_associated | relid=0 | w=20
  227. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:russell-silver syndrome
    n1=en:dysmorphism | n2=en:russell-silver syndrome | rel=r_associated | relid=0 | w=20
  228. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:schinzel-giedion midface-retraction syndrome
    n1=en:dysmorphism | n2=en:schinzel-giedion midface-retraction syndrome | rel=r_associated | relid=0 | w=20
  229. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:situs inversus
    n1=en:dysmorphism | n2=en:situs inversus | rel=r_associated | relid=0 | w=20
  230. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:situs inversus viscerum
    n1=en:dysmorphism | n2=en:situs inversus viscerum | rel=r_associated | relid=0 | w=20
  231. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:situs mutatus
    n1=en:dysmorphism | n2=en:situs mutatus | rel=r_associated | relid=0 | w=20
  232. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:smooth philtrum
    n1=en:dysmorphism | n2=en:smooth philtrum | rel=r_associated | relid=0 | w=20
  233. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:Soto's syndrome
    n1=en:dysmorphism | n2=en:Soto's syndrome | rel=r_associated | relid=0 | w=20
  234. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:sotos' syndrome
    n1=en:dysmorphism | n2=en:sotos' syndrome | rel=r_associated | relid=0 | w=20
  235. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:Sotos' syndrome
    n1=en:dysmorphism | n2=en:Sotos' syndrome | rel=r_associated | relid=0 | w=20
  236. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:stomatognathic system abnormalities
    n1=en:dysmorphism | n2=en:stomatognathic system abnormalities | rel=r_associated | relid=0 | w=20
  237. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:strabismus syndrome
    n1=en:dysmorphism | n2=en:strabismus syndrome | rel=r_associated | relid=0 | w=20
  238. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:supernumerary structure
    n1=en:dysmorphism | n2=en:supernumerary structure | rel=r_associated | relid=0 | w=20
  239. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:telecanthus
    n1=en:dysmorphism | n2=en:telecanthus | rel=r_associated | relid=0 | w=20
  240. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:teratosis
    n1=en:dysmorphism | n2=en:teratosis | rel=r_associated | relid=0 | w=20
  241. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:tetralogy
    n1=en:dysmorphism | n2=en:tetralogy | rel=r_associated | relid=0 | w=20
  242. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:tetralogy of Fallot
    n1=en:dysmorphism | n2=en:tetralogy of Fallot | rel=r_associated | relid=0 | w=20
  243. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:tetralogy of fallot
    n1=en:dysmorphism | n2=en:tetralogy of fallot | rel=r_associated | relid=0 | w=20
  244. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:thyroid dysgenesis
    n1=en:dysmorphism | n2=en:thyroid dysgenesis | rel=r_associated | relid=0 | w=20
  245. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:trichorhinophalangeal syndrome
    n1=en:dysmorphism | n2=en:trichorhinophalangeal syndrome | rel=r_associated | relid=0 | w=20
  246. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:umbilical hernia
    n1=en:dysmorphism | n2=en:umbilical hernia | rel=r_associated | relid=0 | w=20
  247. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:Umbilical hernia
    n1=en:dysmorphism | n2=en:Umbilical hernia | rel=r_associated | relid=0 | w=20
  248. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:umbilical hiatus
    n1=en:dysmorphism | n2=en:umbilical hiatus | rel=r_associated | relid=0 | w=20
  249. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:ureterocele
    n1=en:dysmorphism | n2=en:ureterocele | rel=r_associated | relid=0 | w=20
  250. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:ventriculomeglia
    n1=en:dysmorphism | n2=en:ventriculomeglia | rel=r_associated | relid=0 | w=20
  251. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:wildervanck's syndrome
    n1=en:dysmorphism | n2=en:wildervanck's syndrome | rel=r_associated | relid=0 | w=20
  252. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:with growth retardation
    n1=en:dysmorphism | n2=en:with growth retardation | rel=r_associated | relid=0 | w=20
  253. en:dysmorphism -- r_associated #0: 20 / 0.476 -> en:X-linked
    n1=en:dysmorphism | n2=en:X-linked | rel=r_associated | relid=0 | w=20
  254. en:dysmorphism -- r_associated #0: 20 / 0.476 -> exencéphalie
    n1=en:dysmorphism | n2=exencéphalie | rel=r_associated | relid=0 | w=20
  255. en:dysmorphism -- r_associated #0: 20 / 0.476 -> exomphale
    n1=en:dysmorphism | n2=exomphale | rel=r_associated | relid=0 | w=20
  256. en:dysmorphism -- r_associated #0: 20 / 0.476 -> exomphale congénitale
    n1=en:dysmorphism | n2=exomphale congénitale | rel=r_associated | relid=0 | w=20
  257. en:dysmorphism -- r_associated #0: 20 / 0.476 -> exstrophie
    n1=en:dysmorphism | n2=exstrophie | rel=r_associated | relid=0 | w=20
  258. en:dysmorphism -- r_associated #0: 20 / 0.476 -> faciès anormal, retard de croissance et retard mental
    n1=en:dysmorphism | n2=faciès anormal, retard de croissance et retard mental | rel=r_associated | relid=0 | w=20
  259. en:dysmorphism -- r_associated #0: 20 / 0.476 -> fissure faciale
    n1=en:dysmorphism | n2=fissure faciale | rel=r_associated | relid=0 | w=20
  260. en:dysmorphism -- r_associated #0: 20 / 0.476 -> gigantisme cérébral
    n1=en:dysmorphism | n2=gigantisme cérébral | rel=r_associated | relid=0 | w=20
  261. en:dysmorphism -- r_associated #0: 20 / 0.476 -> hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale
    n1=en:dysmorphism | n2=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | rel=r_associated | relid=0 | w=20
  262. en:dysmorphism -- r_associated #0: 20 / 0.476 -> hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle
    n1=en:dysmorphism | n2=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | rel=r_associated | relid=0 | w=20
  263. en:dysmorphism -- r_associated #0: 20 / 0.476 -> hernie ombilicale
    n1=en:dysmorphism | n2=hernie ombilicale | rel=r_associated | relid=0 | w=20
  264. en:dysmorphism -- r_associated #0: 20 / 0.476 -> hernie ombilicale congénitale
    n1=en:dysmorphism | n2=hernie ombilicale congénitale | rel=r_associated | relid=0 | w=20
  265. en:dysmorphism -- r_associated #0: 20 / 0.476 -> hernies ombilicales
    n1=en:dysmorphism | n2=hernies ombilicales | rel=r_associated | relid=0 | w=20
  266. en:dysmorphism -- r_associated #0: 20 / 0.476 -> hétérotaxie
    n1=en:dysmorphism | n2=hétérotaxie | rel=r_associated | relid=0 | w=20
  267. en:dysmorphism -- r_associated #0: 20 / 0.476 -> hydrocéphalie
    n1=en:dysmorphism | n2=hydrocéphalie | rel=r_associated | relid=0 | w=20
  268. en:dysmorphism -- r_associated #0: 20 / 0.476 -> hypertélorisme
    n1=en:dysmorphism | n2=hypertélorisme | rel=r_associated | relid=0 | w=20
  269. en:dysmorphism -- r_associated #0: 20 / 0.476 -> hypertélorisme-microtie-fente faciale
    n1=en:dysmorphism | n2=hypertélorisme-microtie-fente faciale | rel=r_associated | relid=0 | w=20
  270. en:dysmorphism -- r_associated #0: 20 / 0.476 -> hypertélorisme, hypospadias, polysyndactylie (syndrome)
    n1=en:dysmorphism | n2=hypertélorisme, hypospadias, polysyndactylie (syndrome) | rel=r_associated | relid=0 | w=20
  271. en:dysmorphism -- r_associated #0: 20 / 0.476 -> hypertrophie staturale avec macroglossie et omphalocèle
    n1=en:dysmorphism | n2=hypertrophie staturale avec macroglossie et omphalocèle | rel=r_associated | relid=0 | w=20
  272. en:dysmorphism -- r_associated #0: 20 / 0.476 -> hypoplasie
    n1=en:dysmorphism | n2=hypoplasie | rel=r_associated | relid=0 | w=20
  273. en:dysmorphism -- r_associated #0: 20 / 0.476 -> imperforation anale
    n1=en:dysmorphism | n2=imperforation anale | rel=r_associated | relid=0 | w=20
  274. en:dysmorphism -- r_associated #0: 20 / 0.476 -> imperforation de l'anus
    n1=en:dysmorphism | n2=imperforation de l'anus | rel=r_associated | relid=0 | w=20
  275. en:dysmorphism -- r_associated #0: 20 / 0.476 -> jumeaux fusionnés
    n1=en:dysmorphism | n2=jumeaux fusionnés | rel=r_associated | relid=0 | w=20
  276. en:dysmorphism -- r_associated #0: 20 / 0.476 -> jumeaux siamois
    n1=en:dysmorphism | n2=jumeaux siamois | rel=r_associated | relid=0 | w=20
  277. en:dysmorphism -- r_associated #0: 20 / 0.476 -> macroglossie
    n1=en:dysmorphism | n2=macroglossie | rel=r_associated | relid=0 | w=20
  278. en:dysmorphism -- r_associated #0: 20 / 0.476 -> maladie cardiaque
    n1=en:dysmorphism | n2=maladie cardiaque | rel=r_associated | relid=0 | w=20
  279. en:dysmorphism -- r_associated #0: 20 / 0.476 -> maladie cardiaque non précisée
    n1=en:dysmorphism | n2=maladie cardiaque non précisée | rel=r_associated | relid=0 | w=20
  280. en:dysmorphism -- r_associated #0: 20 / 0.476 -> maladie congénitale
    n1=en:dysmorphism | n2=maladie congénitale | rel=r_associated | relid=0 | w=20
  281. en:dysmorphism -- r_associated #0: 20 / 0.476 -> Maladie congénitale
    n1=en:dysmorphism | n2=Maladie congénitale | rel=r_associated | relid=0 | w=20
  282. en:dysmorphism -- r_associated #0: 20 / 0.476 -> maladie de coeur
    n1=en:dysmorphism | n2=maladie de coeur | rel=r_associated | relid=0 | w=20
  283. en:dysmorphism -- r_associated #0: 20 / 0.476 -> maladie de Roger
    n1=en:dysmorphism | n2=maladie de Roger | rel=r_associated | relid=0 | w=20
  284. en:dysmorphism -- r_associated #0: 20 / 0.476 -> maladie du coeur
    n1=en:dysmorphism | n2=maladie du coeur | rel=r_associated | relid=0 | w=20
  285. en:dysmorphism -- r_associated #0: 20 / 0.476 -> maladies cardiaques
    n1=en:dysmorphism | n2=maladies cardiaques | rel=r_associated | relid=0 | w=20
  286. en:dysmorphism -- r_associated #0: 20 / 0.476 -> maladies des bandes amniotiques
    n1=en:dysmorphism | n2=maladies des bandes amniotiques | rel=r_associated | relid=0 | w=20
  287. en:dysmorphism -- r_associated #0: 20 / 0.476 -> maladies du coeur
    n1=en:dysmorphism | n2=maladies du coeur | rel=r_associated | relid=0 | w=20
  288. en:dysmorphism -- r_associated #0: 20 / 0.476 -> malformation
    n1=en:dysmorphism | n2=malformation | rel=r_associated | relid=0 | w=20
  289. en:dysmorphism -- r_associated #0: 20 / 0.476 -> malformation congénitale
    n1=en:dysmorphism | n2=malformation congénitale | rel=r_associated | relid=0 | w=20
  290. en:dysmorphism -- r_associated #0: 20 / 0.476 -> microdélétion 5q35
    n1=en:dysmorphism | n2=microdélétion 5q35 | rel=r_associated | relid=0 | w=20
  291. en:dysmorphism -- r_associated #0: 20 / 0.476 -> nanisme, retard mental, anomalies oculaires
    n1=en:dysmorphism | n2=nanisme, retard mental, anomalies oculaires | rel=r_associated | relid=0 | w=20
  292. en:dysmorphism -- r_associated #0: 20 / 0.476 -> nystagmus congénital isolé
    n1=en:dysmorphism | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
  293. en:dysmorphism -- r_associated #0: 20 / 0.476 -> oligophrénie
    n1=en:dysmorphism | n2=oligophrénie | rel=r_associated | relid=0 | w=20
  294. en:dysmorphism -- r_associated #0: 20 / 0.476 -> omphalocèle
    n1=en:dysmorphism | n2=omphalocèle | rel=r_associated | relid=0 | w=20
  295. en:dysmorphism -- r_associated #0: 20 / 0.476 -> omphalocèles
    n1=en:dysmorphism | n2=omphalocèles | rel=r_associated | relid=0 | w=20
  296. en:dysmorphism -- r_associated #0: 20 / 0.476 -> onycho-ostéodysostose
    n1=en:dysmorphism | n2=onycho-ostéodysostose | rel=r_associated | relid=0 | w=20
  297. en:dysmorphism -- r_associated #0: 20 / 0.476 -> onycho-patellaire (syndrome)
    n1=en:dysmorphism | n2=onycho-patellaire (syndrome) | rel=r_associated | relid=0 | w=20
  298. en:dysmorphism -- r_associated #0: 20 / 0.476 -> otocéphale
    n1=en:dysmorphism | n2=otocéphale | rel=r_associated | relid=0 | w=20
  299. en:dysmorphism -- r_associated #0: 20 / 0.476 -> otocéphalie
    n1=en:dysmorphism | n2=otocéphalie | rel=r_associated | relid=0 | w=20
  300. en:dysmorphism -- r_associated #0: 20 / 0.476 -> pathologie congénitale
    n1=en:dysmorphism | n2=pathologie congénitale | rel=r_associated | relid=0 | w=20
  301. en:dysmorphism -- r_associated #0: 20 / 0.476 -> pathologie du coeur
    n1=en:dysmorphism | n2=pathologie du coeur | rel=r_associated | relid=0 | w=20
  302. en:dysmorphism -- r_associated #0: 20 / 0.476 -> phacomatose congenitale
    n1=en:dysmorphism | n2=phacomatose congenitale | rel=r_associated | relid=0 | w=20
  303. en:dysmorphism -- r_associated #0: 20 / 0.476 -> Puberté précoce
    n1=en:dysmorphism | n2=Puberté précoce | rel=r_associated | relid=0 | w=20
  304. en:dysmorphism -- r_associated #0: 20 / 0.476 -> puberté précoce
    n1=en:dysmorphism | n2=puberté précoce | rel=r_associated | relid=0 | w=20
  305. en:dysmorphism -- r_associated #0: 20 / 0.476 -> retard mental
    n1=en:dysmorphism | n2=retard mental | rel=r_associated | relid=0 | w=20
  306. en:dysmorphism -- r_associated #0: 20 / 0.476 -> Retard mental
    n1=en:dysmorphism | n2=Retard mental | rel=r_associated | relid=0 | w=20
  307. en:dysmorphism -- r_associated #0: 20 / 0.476 -> retard mental, retard de croissance, surdité, microgénitalisme lié au sexe
    n1=en:dysmorphism | n2=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | rel=r_associated | relid=0 | w=20
  308. en:dysmorphism -- r_associated #0: 20 / 0.476 -> retardation mentale
    n1=en:dysmorphism | n2=retardation mentale | rel=r_associated | relid=0 | w=20
  309. en:dysmorphism -- r_associated #0: 20 / 0.476 -> section 3-1 maladies cardiaques
    n1=en:dysmorphism | n2=section 3-1 maladies cardiaques | rel=r_associated | relid=0 | w=20
  310. en:dysmorphism -- r_associated #0: 20 / 0.476 -> Section 3-1 Maladies cardiaques
    n1=en:dysmorphism | n2=Section 3-1 Maladies cardiaques | rel=r_associated | relid=0 | w=20
  311. en:dysmorphism -- r_associated #0: 20 / 0.476 -> Silver-Russell (syndrome de)
    n1=en:dysmorphism | n2=Silver-Russell (syndrome de) | rel=r_associated | relid=0 | w=20
  312. en:dysmorphism -- r_associated #0: 20 / 0.476 -> sirénomélie
    n1=en:dysmorphism | n2=sirénomélie | rel=r_associated | relid=0 | w=20
  313. en:dysmorphism -- r_associated #0: 20 / 0.476 -> situs inversus
    n1=en:dysmorphism | n2=situs inversus | rel=r_associated | relid=0 | w=20
  314. en:dysmorphism -- r_associated #0: 20 / 0.476 -> situs mutatus
    n1=en:dysmorphism | n2=situs mutatus | rel=r_associated | relid=0 | w=20
  315. en:dysmorphism -- r_associated #0: 20 / 0.476 -> Sotos (syndrome de)
    n1=en:dysmorphism | n2=Sotos (syndrome de) | rel=r_associated | relid=0 | w=20
  316. en:dysmorphism -- r_associated #0: 20 / 0.476 -> sténose du pylore
    n1=en:dysmorphism | n2=sténose du pylore | rel=r_associated | relid=0 | w=20
  317. en:dysmorphism -- r_associated #0: 20 / 0.476 -> sténose pylorique
    n1=en:dysmorphism | n2=sténose pylorique | rel=r_associated | relid=0 | w=20
  318. en:dysmorphism -- r_associated #0: 20 / 0.476 -> syndrome de bride amniotique
    n1=en:dysmorphism | n2=syndrome de bride amniotique | rel=r_associated | relid=0 | w=20
  319. en:dysmorphism -- r_associated #0: 20 / 0.476 -> syndrome de silver-russell
    n1=en:dysmorphism | n2=syndrome de silver-russell | rel=r_associated | relid=0 | w=20
  320. en:dysmorphism -- r_associated #0: 20 / 0.476 -> syndrome de Silver-Russell
    n1=en:dysmorphism | n2=syndrome de Silver-Russell | rel=r_associated | relid=0 | w=20
  321. en:dysmorphism -- r_associated #0: 20 / 0.476 -> syndrome de soto
    n1=en:dysmorphism | n2=syndrome de soto | rel=r_associated | relid=0 | w=20
  322. en:dysmorphism -- r_associated #0: 20 / 0.476 -> syndrome de Sotos
    n1=en:dysmorphism | n2=syndrome de Sotos | rel=r_associated | relid=0 | w=20
  323. en:dysmorphism -- r_associated #0: 20 / 0.476 -> syndrome de sotos
    n1=en:dysmorphism | n2=syndrome de sotos | rel=r_associated | relid=0 | w=20
  324. en:dysmorphism -- r_associated #0: 20 / 0.476 -> syndrome des brides amniotiques
    n1=en:dysmorphism | n2=syndrome des brides amniotiques | rel=r_associated | relid=0 | w=20
  325. en:dysmorphism -- r_associated #0: 20 / 0.476 -> tare congénitale
    n1=en:dysmorphism | n2=tare congénitale | rel=r_associated | relid=0 | w=20
  326. en:dysmorphism -- r_associated #0: 20 / 0.476 -> télécanthus-hypertélorisme-strabisme (syndrome)
    n1=en:dysmorphism | n2=télécanthus-hypertélorisme-strabisme (syndrome) | rel=r_associated | relid=0 | w=20
  327. en:dysmorphism -- r_associated #0: 20 / 0.476 -> tétralogie de Fallot
    n1=en:dysmorphism | n2=tétralogie de Fallot | rel=r_associated | relid=0 | w=20
  328. en:dysmorphism -- r_associated #0: 20 / 0.476 -> tétralogie de fallot
    n1=en:dysmorphism | n2=tétralogie de fallot | rel=r_associated | relid=0 | w=20
  329. en:dysmorphism -- r_associated #0: 20 / 0.476 -> trouble cardiaque
    n1=en:dysmorphism | n2=trouble cardiaque | rel=r_associated | relid=0 | w=20
  330. en:dysmorphism -- r_associated #0: 20 / 0.476 -> trouble chromosomique
    n1=en:dysmorphism | n2=trouble chromosomique | rel=r_associated | relid=0 | w=20
  331. en:dysmorphism -- r_associated #0: 20 / 0.476 -> troubles endocriniens, épilepsie et déficience mentale
    n1=en:dysmorphism | n2=troubles endocriniens, épilepsie et déficience mentale | rel=r_associated | relid=0 | w=20
  332. en:dysmorphism -- r_associated #0: 20 / 0.476 -> urétérocèle
    n1=en:dysmorphism | n2=urétérocèle | rel=r_associated | relid=0 | w=20
  333. en:dysmorphism -- r_associated #0: 20 / 0.476 -> ventriculomégalie cérébrale
    n1=en:dysmorphism | n2=ventriculomégalie cérébrale | rel=r_associated | relid=0 | w=20
  334. en:dysmorphism -- r_associated #0: 20 / 0.476 -> vice de conformation
    n1=en:dysmorphism | n2=vice de conformation | rel=r_associated | relid=0 | w=20
≈ 560 relations entrantes

  1. anomalie congénitale --- r_associated #0: 424 --> en:dysmorphism
    n1=anomalie congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=424
  2. en:congenital abnormality --- r_associated #0: 420 --> en:dysmorphism
    n1=en:congenital abnormality | n2=en:dysmorphism | rel=r_associated | relid=0 | w=420
  3. anomalie cardiaque --- r_associated #0: 356 --> en:dysmorphism
    n1=anomalie cardiaque | n2=en:dysmorphism | rel=r_associated | relid=0 | w=356
  4. malformation congénitale --- r_associated #0: 356 --> en:dysmorphism
    n1=malformation congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=356
  5. card --- r_associated #0: 355 --> en:dysmorphism
    n1=card | n2=en:dysmorphism | rel=r_associated | relid=0 | w=355
  6. en:heart disorder --- r_associated #0: 355 --> en:dysmorphism
    n1=en:heart disorder | n2=en:dysmorphism | rel=r_associated | relid=0 | w=355
  7. maladie cardiaque non précisée --- r_associated #0: 355 --> en:dysmorphism
    n1=maladie cardiaque non précisée | n2=en:dysmorphism | rel=r_associated | relid=0 | w=355
  8. maladie du coeur --- r_associated #0: 355 --> en:dysmorphism
    n1=maladie du coeur | n2=en:dysmorphism | rel=r_associated | relid=0 | w=355
  9. en:congenital anomaly --- r_associated #0: 352 --> en:dysmorphism
    n1=en:congenital anomaly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=352
  10. en:heart malformation --- r_associated #0: 348 --> en:dysmorphism
    n1=en:heart malformation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=348
  11. affection cardiaque --- r_associated #0: 345 --> en:dysmorphism
    n1=affection cardiaque | n2=en:dysmorphism | rel=r_associated | relid=0 | w=345
  12. anomalie du coeur --- r_associated #0: 345 --> en:dysmorphism
    n1=anomalie du coeur | n2=en:dysmorphism | rel=r_associated | relid=0 | w=345
  13. malformation cardiaque --- r_associated #0: 339 --> en:dysmorphism
    n1=malformation cardiaque | n2=en:dysmorphism | rel=r_associated | relid=0 | w=339
  14. maladie cardiaque --- r_associated #0: 335 --> en:dysmorphism
    n1=maladie cardiaque | n2=en:dysmorphism | rel=r_associated | relid=0 | w=335
  15. trouble cardiaque --- r_associated #0: 335 --> en:dysmorphism
    n1=trouble cardiaque | n2=en:dysmorphism | rel=r_associated | relid=0 | w=335
  16. cardiopathie --- r_associated #0: 325 --> en:dysmorphism
    n1=cardiopathie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=325
  17. en:heart diseases --- r_associated #0: 325 --> en:dysmorphism
    n1=en:heart diseases | n2=en:dysmorphism | rel=r_associated | relid=0 | w=325
  18. pathologie du coeur --- r_associated #0: 325 --> en:dysmorphism
    n1=pathologie du coeur | n2=en:dysmorphism | rel=r_associated | relid=0 | w=325
  19. en:congenital defect --- r_associated #0: 310 --> en:dysmorphism
    n1=en:congenital defect | n2=en:dysmorphism | rel=r_associated | relid=0 | w=310
  20. déformation congénitale --- r_associated #0: 286 --> en:dysmorphism
    n1=déformation congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=286
  21. section 3-1 maladies cardiaques --- r_associated #0: 280 --> en:dysmorphism
    n1=section 3-1 maladies cardiaques | n2=en:dysmorphism | rel=r_associated | relid=0 | w=280
  22. déficience congénitale --- r_associated #0: 275 --> en:dysmorphism
    n1=déficience congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=275
  23. crânio-sténose --- r_associated #0: 254 --> en:dysmorphism
    n1=crânio-sténose | n2=en:dysmorphism | rel=r_associated | relid=0 | w=254
  24. crâniosténose --- r_associated #0: 254 --> en:dysmorphism
    n1=crâniosténose | n2=en:dysmorphism | rel=r_associated | relid=0 | w=254
  25. en:craniosynostosis --- r_associated #0: 254 --> en:dysmorphism
    n1=en:craniosynostosis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=254
  26. crâniosynostose --- r_associated #0: 251 --> en:dysmorphism
    n1=crâniosynostose | n2=en:dysmorphism | rel=r_associated | relid=0 | w=251
  27. craniosynostose --- r_associated #0: 245 --> en:dysmorphism
    n1=craniosynostose | n2=en:dysmorphism | rel=r_associated | relid=0 | w=245
  28. exomphale --- r_associated #0: 220 --> en:dysmorphism
    n1=exomphale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=220
  29. omphalocèles --- r_associated #0: 216 --> en:dysmorphism
    n1=omphalocèles | n2=en:dysmorphism | rel=r_associated | relid=0 | w=216
  30. en:omphalocele --- r_associated #0: 210 --> en:dysmorphism
    n1=en:omphalocele | n2=en:dysmorphism | rel=r_associated | relid=0 | w=210
  31. hernie ombilicale --- r_associated #0: 210 --> en:dysmorphism
    n1=hernie ombilicale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=210
  32. hernie ombilicale congénitale --- r_associated #0: 210 --> en:dysmorphism
    n1=hernie ombilicale congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=210
  33. omphalocèle --- r_associated #0: 210 --> en:dysmorphism
    n1=omphalocèle | n2=en:dysmorphism | rel=r_associated | relid=0 | w=210
  34. anomalie congénitale de l'oeil --- r_associated #0: 209 --> en:dysmorphism
    n1=anomalie congénitale de l'oeil | n2=en:dysmorphism | rel=r_associated | relid=0 | w=209
  35. en:congenital eye disorder --- r_associated #0: 205 --> en:dysmorphism
    n1=en:congenital eye disorder | n2=en:dysmorphism | rel=r_associated | relid=0 | w=205
  36. hernies ombilicales --- r_associated #0: 201 --> en:dysmorphism
    n1=hernies ombilicales | n2=en:dysmorphism | rel=r_associated | relid=0 | w=201
  37. affections cardiaques --- r_associated #0: 200 --> en:dysmorphism
    n1=affections cardiaques | n2=en:dysmorphism | rel=r_associated | relid=0 | w=200
  38. en:umbilical hernia --- r_associated #0: 200 --> en:dysmorphism
    n1=en:umbilical hernia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=200
  39. exomphale congénitale --- r_associated #0: 200 --> en:dysmorphism
    n1=exomphale congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=200
  40. maladies du coeur --- r_associated #0: 195 --> en:dysmorphism
    n1=maladies du coeur | n2=en:dysmorphism | rel=r_associated | relid=0 | w=195
  41. en:sotos syndrome --- r_associated #0: 191 --> en:dysmorphism
    n1=en:sotos syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=191
  42. difformité congénitale --- r_associated #0: 190 --> en:dysmorphism
    n1=difformité congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=190
  43. maladie congénitale --- r_associated #0: 190 --> en:dysmorphism
    n1=maladie congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=190
  44. maladies cardiaques --- r_associated #0: 190 --> en:dysmorphism
    n1=maladies cardiaques | n2=en:dysmorphism | rel=r_associated | relid=0 | w=190
  45. syndrome de soto --- r_associated #0: 190 --> en:dysmorphism
    n1=syndrome de soto | n2=en:dysmorphism | rel=r_associated | relid=0 | w=190
  46. hypoplasie --- r_associated #0: 189 --> en:dysmorphism
    n1=hypoplasie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=189
  47. gigantisme cérébral --- r_associated #0: 186 --> en:dysmorphism
    n1=gigantisme cérébral | n2=en:dysmorphism | rel=r_associated | relid=0 | w=186
  48. cardiopathies --- r_associated #0: 185 --> en:dysmorphism
    n1=cardiopathies | n2=en:dysmorphism | rel=r_associated | relid=0 | w=185
  49. craniosténose --- r_associated #0: 185 --> en:dysmorphism
    n1=craniosténose | n2=en:dysmorphism | rel=r_associated | relid=0 | w=185
  50. en:hypoplasia --- r_associated #0: 185 --> en:dysmorphism
    n1=en:hypoplasia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=185
  51. pathologie congénitale --- r_associated #0: 185 --> en:dysmorphism
    n1=pathologie congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=185
  52. syndrome de Sotos --- r_associated #0: 185 --> en:dysmorphism
    n1=syndrome de Sotos | n2=en:dysmorphism | rel=r_associated | relid=0 | w=185
  53. affection oculaire congénitale --- r_associated #0: 180 --> en:dysmorphism
    n1=affection oculaire congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=180
  54. en:sotos' syndrome --- r_associated #0: 180 --> en:dysmorphism
    n1=en:sotos' syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=180
  55. en:heart disease --- r_associated #0: 175 --> en:dysmorphism
    n1=en:heart disease | n2=en:dysmorphism | rel=r_associated | relid=0 | w=175
  56. en:card --- r_associated #0: 170 --> en:dysmorphism
    n1=en:card | n2=en:dysmorphism | rel=r_associated | relid=0 | w=170
  57. anomalie chromosomique --- r_associated #0: 166 --> en:dysmorphism
    n1=anomalie chromosomique | n2=en:dysmorphism | rel=r_associated | relid=0 | w=166
  58. en:chromosomal abnormality --- r_associated #0: 165 --> en:dysmorphism
    n1=en:chromosomal abnormality | n2=en:dysmorphism | rel=r_associated | relid=0 | w=165
  59. en:arthrogryposis --- r_associated #0: 157 --> en:dysmorphism
    n1=en:arthrogryposis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=157
  60. arthrogrypose --- r_associated #0: 155 --> en:dysmorphism
    n1=arthrogrypose | n2=en:dysmorphism | rel=r_associated | relid=0 | w=155
  61. Retard mental --- r_associated #0: 130 --> en:dysmorphism
    n1=Retard mental | n2=en:dysmorphism | rel=r_associated | relid=0 | w=130
  62. en:congenital malformation --- r_associated #0: 130 --> en:dysmorphism
    n1=en:congenital malformation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=130
  63. retard mental --- r_associated #0: 130 --> en:dysmorphism
    n1=retard mental | n2=en:dysmorphism | rel=r_associated | relid=0 | w=130
  64. en:mental retardation --- r_associated #0: 129 --> en:dysmorphism
    n1=en:mental retardation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=129
  65. retardation mentale --- r_associated #0: 129 --> en:dysmorphism
    n1=retardation mentale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=129
  66. situs inversus --- r_associated #0: 122 --> en:dysmorphism
    n1=situs inversus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=122
  67. en:birth defect --- r_associated #0: 120 --> en:dysmorphism
    n1=en:birth defect | n2=en:dysmorphism | rel=r_associated | relid=0 | w=120
  68. en:situs inversus --- r_associated #0: 119 --> en:dysmorphism
    n1=en:situs inversus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=119
  69. otocéphale --- r_associated #0: 116 --> en:dysmorphism
    n1=otocéphale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=116
  70. ancyloglosse --- r_associated #0: 111 --> en:dysmorphism
    n1=ancyloglosse | n2=en:dysmorphism | rel=r_associated | relid=0 | w=111
  71. ankyloglosse --- r_associated #0: 111 --> en:dysmorphism
    n1=ankyloglosse | n2=en:dysmorphism | rel=r_associated | relid=0 | w=111
  72. en:ankyloglossia --- r_associated #0: 107 --> en:dysmorphism
    n1=en:ankyloglossia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=107
  73. otocéphalie --- r_associated #0: 106 --> en:dysmorphism
    n1=otocéphalie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=106
  74. en:otocephaly --- r_associated #0: 103 --> en:dysmorphism
    n1=en:otocephaly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=103
  75. exencéphalie --- r_associated #0: 103 --> en:dysmorphism
    n1=exencéphalie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=103
  76. en:exencephaly --- r_associated #0: 100 --> en:dysmorphism
    n1=en:exencephaly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=100
  77. en:pyloric stenosis --- r_associated #0: 98 --> en:dysmorphism
    n1=en:pyloric stenosis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=98
  78. hypertélorisme --- r_associated #0: 96 --> en:dysmorphism
    n1=hypertélorisme | n2=en:dysmorphism | rel=r_associated | relid=0 | w=96
  79. en:chromosome disorder --- r_associated #0: 95 --> en:dysmorphism
    n1=en:chromosome disorder | n2=en:dysmorphism | rel=r_associated | relid=0 | w=95
  80. sténose du pylore --- r_associated #0: 95 --> en:dysmorphism
    n1=sténose du pylore | n2=en:dysmorphism | rel=r_associated | relid=0 | w=95
  81. sténose pylorique --- r_associated #0: 95 --> en:dysmorphism
    n1=sténose pylorique | n2=en:dysmorphism | rel=r_associated | relid=0 | w=95
  82. trouble chromosomique --- r_associated #0: 95 --> en:dysmorphism
    n1=trouble chromosomique | n2=en:dysmorphism | rel=r_associated | relid=0 | w=95
  83. tétralogie de Fallot --- r_associated #0: 95 --> en:dysmorphism
    n1=tétralogie de Fallot | n2=en:dysmorphism | rel=r_associated | relid=0 | w=95
  84. en:hypertelorism --- r_associated #0: 93 --> en:dysmorphism
    n1=en:hypertelorism | n2=en:dysmorphism | rel=r_associated | relid=0 | w=93
  85. en:tetralogy of fallot --- r_associated #0: 91 --> en:dysmorphism
    n1=en:tetralogy of fallot | n2=en:dysmorphism | rel=r_associated | relid=0 | w=91
  86. tétralogie de fallot --- r_associated #0: 91 --> en:dysmorphism
    n1=tétralogie de fallot | n2=en:dysmorphism | rel=r_associated | relid=0 | w=91
  87. anormalité des chromosomes --- r_associated #0: 90 --> en:dysmorphism
    n1=anormalité des chromosomes | n2=en:dysmorphism | rel=r_associated | relid=0 | w=90
  88. en:tetralogy of Fallot --- r_associated #0: 90 --> en:dysmorphism
    n1=en:tetralogy of Fallot | n2=en:dysmorphism | rel=r_associated | relid=0 | w=90
  89. Section 3-1 Maladies cardiaques --- r_associated #0: 85 --> en:dysmorphism
    n1=Section 3-1 Maladies cardiaques | n2=en:dysmorphism | rel=r_associated | relid=0 | w=85
  90. en:Umbilical hernia --- r_associated #0: 85 --> en:dysmorphism
    n1=en:Umbilical hernia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=85
  91. en:tetralogy --- r_associated #0: 85 --> en:dysmorphism
    n1=en:tetralogy | n2=en:dysmorphism | rel=r_associated | relid=0 | w=85
  92. en:ventriculomeglia --- r_associated #0: 84 --> en:dysmorphism
    n1=en:ventriculomeglia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=84
  93. en:Fallot's disease --- r_associated #0: 80 --> en:dysmorphism
    n1=en:Fallot's disease | n2=en:dysmorphism | rel=r_associated | relid=0 | w=80
  94. en:cerebral ventriculomegaly --- r_associated #0: 80 --> en:dysmorphism
    n1=en:cerebral ventriculomegaly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=80
  95. hydrocéphalie --- r_associated #0: 80 --> en:dysmorphism
    n1=hydrocéphalie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=80
  96. tare congénitale --- r_associated #0: 80 --> en:dysmorphism
    n1=tare congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=80
  97. troubles du myocarde --- r_associated #0: 80 --> en:dysmorphism
    n1=troubles du myocarde | n2=en:dysmorphism | rel=r_associated | relid=0 | w=80
  98. ventriculomégalie cérébrale --- r_associated #0: 79 --> en:dysmorphism
    n1=ventriculomégalie cérébrale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=79
  99. en:pyloric obstruction --- r_associated #0: 75 --> en:dysmorphism
    n1=en:pyloric obstruction | n2=en:dysmorphism | rel=r_associated | relid=0 | w=75
  100. albinisme --- r_associated #0: 74 --> en:dysmorphism
    n1=albinisme | n2=en:dysmorphism | rel=r_associated | relid=0 | w=74
  101. en:albinism --- r_associated #0: 72 --> en:dysmorphism
    n1=en:albinism | n2=en:dysmorphism | rel=r_associated | relid=0 | w=72
  102. en:ectopia cordis --- r_associated #0: 72 --> en:dysmorphism
    n1=en:ectopia cordis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=72
  103. arriération mentale --- r_associated #0: 71 --> en:dysmorphism
    n1=arriération mentale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=71
  104. débilité mentale --- r_associated #0: 70 --> en:dysmorphism
    n1=débilité mentale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=70
  105. sœurs siamoises --- r_associated #0: 70 --> en:dysmorphism
    n1=sœurs siamoises | n2=en:dysmorphism | rel=r_associated | relid=0 | w=70
  106. ectopia cordis --- r_associated #0: 68 --> en:dysmorphism
    n1=ectopia cordis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=68
  107. en:cyclopia --- r_associated #0: 68 --> en:dysmorphism
    n1=en:cyclopia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=68
  108. en:russell-silver syndrome --- r_associated #0: 66 --> en:dysmorphism
    n1=en:russell-silver syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=66
  109. soeurs siamoises --- r_associated #0: 66 --> en:dysmorphism
    n1=soeurs siamoises | n2=en:dysmorphism | rel=r_associated | relid=0 | w=66
  110. maladie du cœur --- r_associated #0: 65 --> en:dysmorphism
    n1=maladie du cœur | n2=en:dysmorphism | rel=r_associated | relid=0 | w=65
  111. cyclopie --- r_associated #0: 64 --> en:dysmorphism
    n1=cyclopie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=64
  112. syndrome de Silver-Russell --- r_associated #0: 64 --> en:dysmorphism
    n1=syndrome de Silver-Russell | n2=en:dysmorphism | rel=r_associated | relid=0 | w=64
  113. cyclopia --- r_associated #0: 63 --> en:dysmorphism
    n1=cyclopia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=63
  114. anomalie cytogénétique --- r_associated #0: 60 --> en:dysmorphism
    n1=anomalie cytogénétique | n2=en:dysmorphism | rel=r_associated | relid=0 | w=60
  115. en:Sotos' syndrome --- r_associated #0: 60 --> en:dysmorphism
    n1=en:Sotos' syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=60
  116. en:cardiac diseases --- r_associated #0: 60 --> en:dysmorphism
    n1=en:cardiac diseases | n2=en:dysmorphism | rel=r_associated | relid=0 | w=60
  117. congénitale --- r_associated #0: 59 --> en:dysmorphism
    n1=congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=59
  118. en:congenital --- r_associated #0: 59 --> en:dysmorphism
    n1=en:congenital | n2=en:dysmorphism | rel=r_associated | relid=0 | w=59
  119. urétérocèle --- r_associated #0: 59 --> en:dysmorphism
    n1=urétérocèle | n2=en:dysmorphism | rel=r_associated | relid=0 | w=59
  120. congenital --- r_associated #0: 57 --> en:dysmorphism
    n1=congenital | n2=en:dysmorphism | rel=r_associated | relid=0 | w=57
  121. vice de conformation --- r_associated #0: 57 --> en:dysmorphism
    n1=vice de conformation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=57
  122. congénital --- r_associated #0: 55 --> en:dysmorphism
    n1=congénital | n2=en:dysmorphism | rel=r_associated | relid=0 | w=55
  123. en:situs inversus viscerum --- r_associated #0: 55 --> en:dysmorphism
    n1=en:situs inversus viscerum | n2=en:dysmorphism | rel=r_associated | relid=0 | w=55
  124. en:ureterocele --- r_associated #0: 55 --> en:dysmorphism
    n1=en:ureterocele | n2=en:dysmorphism | rel=r_associated | relid=0 | w=55
  125. hypertrophie staturale avec macroglossie et omphalocèle --- r_associated #0: 55 --> en:dysmorphism
    n1=hypertrophie staturale avec macroglossie et omphalocèle | n2=en:dysmorphism | rel=r_associated | relid=0 | w=55
  126. en:situs mutatus --- r_associated #0: 54 --> en:dysmorphism
    n1=en:situs mutatus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=54
  127. syndrome de silver-russell --- r_associated #0: 54 --> en:dysmorphism
    n1=syndrome de silver-russell | n2=en:dysmorphism | rel=r_associated | relid=0 | w=54
  128. ectopie cardiaque --- r_associated #0: 51 --> en:dysmorphism
    n1=ectopie cardiaque | n2=en:dysmorphism | rel=r_associated | relid=0 | w=51
  129. en:exomphalos --- r_associated #0: 50 --> en:dysmorphism
    n1=en:exomphalos | n2=en:dysmorphism | rel=r_associated | relid=0 | w=50
  130. en:macroglossia --- r_associated #0: 50 --> en:dysmorphism
    n1=en:macroglossia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=50
  131. hypertélorisme-microtie-fente faciale --- r_associated #0: 50 --> en:dysmorphism
    n1=hypertélorisme-microtie-fente faciale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=50
  132. anomalie du développement --- r_associated #0: 49 --> en:dysmorphism
    n1=anomalie du développement | n2=en:dysmorphism | rel=r_associated | relid=0 | w=49
  133. en:teratosis --- r_associated #0: 49 --> en:dysmorphism
    n1=en:teratosis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=49
  134. hypertélorisme, hypospadias, polysyndactylie (syndrome) --- r_associated #0: 49 --> en:dysmorphism
    n1=hypertélorisme, hypospadias, polysyndactylie (syndrome) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=49
  135. en:heterotaxy syndrome --- r_associated #0: 48 --> en:dysmorphism
    n1=en:heterotaxy syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=48
  136. syndrome de sotos --- r_associated #0: 48 --> en:dysmorphism
    n1=syndrome de sotos | n2=en:dysmorphism | rel=r_associated | relid=0 | w=48
  137. en:major physical defect --- r_associated #0: 47 --> en:dysmorphism
    n1=en:major physical defect | n2=en:dysmorphism | rel=r_associated | relid=0 | w=47
  138. télécanthus-hypertélorisme-strabisme (syndrome) --- r_associated #0: 47 --> en:dysmorphism
    n1=télécanthus-hypertélorisme-strabisme (syndrome) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=47
  139. en:amniotic band syndrome --- r_associated #0: 46 --> en:dysmorphism
    n1=en:amniotic band syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=46
  140. maladies des bandes amniotiques --- r_associated #0: 46 --> en:dysmorphism
    n1=maladies des bandes amniotiques | n2=en:dysmorphism | rel=r_associated | relid=0 | w=46
  141. retard mental, retard de croissance, surdité, microgénitalisme lié au sexe --- r_associated #0: 46 --> en:dysmorphism
    n1=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | n2=en:dysmorphism | rel=r_associated | relid=0 | w=46
  142. syndrome de bride amniotique --- r_associated #0: 46 --> en:dysmorphism
    n1=syndrome de bride amniotique | n2=en:dysmorphism | rel=r_associated | relid=0 | w=46
  143. syndrome des brides amniotiques --- r_associated #0: 46 --> en:dysmorphism
    n1=syndrome des brides amniotiques | n2=en:dysmorphism | rel=r_associated | relid=0 | w=46
  144. ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) --- r_associated #0: 45 --> en:dysmorphism
    n1=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=45
  145. en:hydrencephalus --- r_associated #0: 45 --> en:dysmorphism
    n1=en:hydrencephalus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=45
  146. en:adrenal cytomegaly --- r_associated #0: 44 --> en:dysmorphism
    n1=en:adrenal cytomegaly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=44
  147. en:physical defect --- r_associated #0: 44 --> en:dysmorphism
    n1=en:physical defect | n2=en:dysmorphism | rel=r_associated | relid=0 | w=44
  148. hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle --- r_associated #0: 44 --> en:dysmorphism
    n1=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | n2=en:dysmorphism | rel=r_associated | relid=0 | w=44
  149. maladie de Roger --- r_associated #0: 44 --> en:dysmorphism
    n1=maladie de Roger | n2=en:dysmorphism | rel=r_associated | relid=0 | w=44
  150. en:aicardi syndrome --- r_associated #0: 42 --> en:dysmorphism
    n1=en:aicardi syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=42
  151. en:gigantism and hyperplastic visceromegaly --- r_associated #0: 42 --> en:dysmorphism
    n1=en:gigantism and hyperplastic visceromegaly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=42
  152. en:infantile fibrosarcoma --- r_associated #0: 42 --> en:dysmorphism
    n1=en:infantile fibrosarcoma | n2=en:dysmorphism | rel=r_associated | relid=0 | w=42
  153. en:neurodevelopmental anomaly --- r_associated #0: 42 --> en:dysmorphism
    n1=en:neurodevelopmental anomaly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=42
  154. faciès anormal, retard de croissance et retard mental --- r_associated #0: 42 --> en:dysmorphism
    n1=faciès anormal, retard de croissance et retard mental | n2=en:dysmorphism | rel=r_associated | relid=0 | w=42
  155. en:ectodermal dysplasia --- r_associated #0: 41 --> en:dysmorphism
    n1=en:ectodermal dysplasia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=41
  156. en:hypertrophy of clitoris --- r_associated #0: 41 --> en:dysmorphism
    n1=en:hypertrophy of clitoris | n2=en:dysmorphism | rel=r_associated | relid=0 | w=41
  157. en:syndrome, mohr --- r_associated #0: 41 --> en:dysmorphism
    n1=en:syndrome, mohr | n2=en:dysmorphism | rel=r_associated | relid=0 | w=41
  158. hétérotaxie --- r_associated #0: 41 --> en:dysmorphism
    n1=hétérotaxie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=41
  159. imperforation anale --- r_associated #0: 41 --> en:dysmorphism
    n1=imperforation anale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=41
  160. en:heterotaxy --- r_associated #0: 40 --> en:dysmorphism
    n1=en:heterotaxy | n2=en:dysmorphism | rel=r_associated | relid=0 | w=40
  161. en:ventricular septal defect --- r_associated #0: 40 --> en:dysmorphism
    n1=en:ventricular septal defect | n2=en:dysmorphism | rel=r_associated | relid=0 | w=40
  162. maladie de cœur --- r_associated #0: 40 --> en:dysmorphism
    n1=maladie de cœur | n2=en:dysmorphism | rel=r_associated | relid=0 | w=40
  163. maladie de coeur --- r_associated #0: 40 --> en:dysmorphism
    n1=maladie de coeur | n2=en:dysmorphism | rel=r_associated | relid=0 | w=40
  164. onycho-ostéodysostose --- r_associated #0: 40 --> en:dysmorphism
    n1=onycho-ostéodysostose | n2=en:dysmorphism | rel=r_associated | relid=0 | w=40
  165. en:hereditary elliptocytosis --- r_associated #0: 39 --> en:dysmorphism
    n1=en:hereditary elliptocytosis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=39
  166. en:telecanthus --- r_associated #0: 39 --> en:dysmorphism
    n1=en:telecanthus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=39
  167. imperforation de l'anus --- r_associated #0: 39 --> en:dysmorphism
    n1=imperforation de l'anus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=39
  168. communication inter-auriculaire --- r_associated #0: 38 --> en:dysmorphism
    n1=communication inter-auriculaire | n2=en:dysmorphism | rel=r_associated | relid=0 | w=38
  169. déficience intellectuelle --- r_associated #0: 38 --> en:dysmorphism
    n1=déficience intellectuelle | n2=en:dysmorphism | rel=r_associated | relid=0 | w=38
  170. fissure faciale --- r_associated #0: 38 --> en:dysmorphism
    n1=fissure faciale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=38
  171. en:ethmocephaly --- r_associated #0: 37 --> en:dysmorphism
    n1=en:ethmocephaly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=37
  172. en:imperforate anus --- r_associated #0: 37 --> en:dysmorphism
    n1=en:imperforate anus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=37
  173. en:nail-patella syndrome --- r_associated #0: 37 --> en:dysmorphism
    n1=en:nail-patella syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=37
  174. Puberté précoce --- r_associated #0: 36 --> en:dysmorphism
    n1=Puberté précoce | n2=en:dysmorphism | rel=r_associated | relid=0 | w=36
  175. communication interauriculaire --- r_associated #0: 36 --> en:dysmorphism
    n1=communication interauriculaire | n2=en:dysmorphism | rel=r_associated | relid=0 | w=36
  176. en:Soto's syndrome --- r_associated #0: 36 --> en:dysmorphism
    n1=en:Soto's syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=36
  177. en:cerebral gigantism --- r_associated #0: 36 --> en:dysmorphism
    n1=en:cerebral gigantism | n2=en:dysmorphism | rel=r_associated | relid=0 | w=36
  178. nystagmus congénital isolé --- r_associated #0: 36 --> en:dysmorphism
    n1=nystagmus congénital isolé | n2=en:dysmorphism | rel=r_associated | relid=0 | w=36
  179. sirénomélie --- r_associated #0: 36 --> en:dysmorphism
    n1=sirénomélie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=36
  180. Maladie congénitale --- r_associated #0: 35 --> en:dysmorphism
    n1=Maladie congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  181. en:cardiovascular abnormalities --- r_associated #0: 35 --> en:dysmorphism
    n1=en:cardiovascular abnormalities | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  182. en:celosomy --- r_associated #0: 35 --> en:dysmorphism
    n1=en:celosomy | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  183. en:congenital deformity of hip --- r_associated #0: 35 --> en:dysmorphism
    n1=en:congenital deformity of hip | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  184. en:congenital enlargement --- r_associated #0: 35 --> en:dysmorphism
    n1=en:congenital enlargement | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  185. en:congenital keratoglobus --- r_associated #0: 35 --> en:dysmorphism
    n1=en:congenital keratoglobus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  186. en:congenital septation --- r_associated #0: 35 --> en:dysmorphism
    n1=en:congenital septation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  187. en:conjoined twins --- r_associated #0: 35 --> en:dysmorphism
    n1=en:conjoined twins | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  188. en:embryonic cyst --- r_associated #0: 35 --> en:dysmorphism
    n1=en:embryonic cyst | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  189. en:failure of the mind --- r_associated #0: 35 --> en:dysmorphism
    n1=en:failure of the mind | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  190. en:intestinal malrotation --- r_associated #0: 35 --> en:dysmorphism
    n1=en:intestinal malrotation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  191. en:mental deficiency --- r_associated #0: 35 --> en:dysmorphism
    n1=en:mental deficiency | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  192. en:musculoskeletal disorders congenital nec --- r_associated #0: 35 --> en:dysmorphism
    n1=en:musculoskeletal disorders congenital nec | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  193. en:supernumerary structure --- r_associated #0: 35 --> en:dysmorphism
    n1=en:supernumerary structure | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  194. en:thyroid dysgenesis --- r_associated #0: 35 --> en:dysmorphism
    n1=en:thyroid dysgenesis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  195. onycho-patellaire (syndrome) --- r_associated #0: 35 --> en:dysmorphism
    n1=onycho-patellaire (syndrome) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=35
  196. en:abnormality, severe teratoid --- r_associated #0: 34 --> en:dysmorphism
    n1=en:abnormality, severe teratoid | n2=en:dysmorphism | rel=r_associated | relid=0 | w=34
  197. en:amegakaryocytic thrombocytopenia with congenital malformation --- r_associated #0: 34 --> en:dysmorphism
    n1=en:amegakaryocytic thrombocytopenia with congenital malformation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=34
  198. en:congenital cardiovascular abnormality --- r_associated #0: 34 --> en:dysmorphism
    n1=en:congenital cardiovascular abnormality | n2=en:dysmorphism | rel=r_associated | relid=0 | w=34
  199. en:congenital macrocephaly --- r_associated #0: 34 --> en:dysmorphism
    n1=en:congenital macrocephaly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=34
  200. en:developmental immaturity --- r_associated #0: 34 --> en:dysmorphism
    n1=en:developmental immaturity | n2=en:dysmorphism | rel=r_associated | relid=0 | w=34
  201. en:facial cleft --- r_associated #0: 34 --> en:dysmorphism
    n1=en:facial cleft | n2=en:dysmorphism | rel=r_associated | relid=0 | w=34
  202. en:hydrocephalus --- r_associated #0: 34 --> en:dysmorphism
    n1=en:hydrocephalus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=34
  203. en:laron syndrome --- r_associated #0: 34 --> en:dysmorphism
    n1=en:laron syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=34
  204. en:schinzel-giedion midface-retraction syndrome --- r_associated #0: 34 --> en:dysmorphism
    n1=en:schinzel-giedion midface-retraction syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=34
  205. en:stomatognathic system abnormalities --- r_associated #0: 34 --> en:dysmorphism
    n1=en:stomatognathic system abnormalities | n2=en:dysmorphism | rel=r_associated | relid=0 | w=34
  206. nanisme, retard mental, anomalies oculaires --- r_associated #0: 34 --> en:dysmorphism
    n1=nanisme, retard mental, anomalies oculaires | n2=en:dysmorphism | rel=r_associated | relid=0 | w=34
  207. Silver-Russell (syndrome de) --- r_associated #0: 33 --> en:dysmorphism
    n1=Silver-Russell (syndrome de) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=33
  208. en:exenkephaly --- r_associated #0: 33 --> en:dysmorphism
    n1=en:exenkephaly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=33
  209. en:precocious puberty --- r_associated #0: 33 --> en:dysmorphism
    n1=en:precocious puberty | n2=en:dysmorphism | rel=r_associated | relid=0 | w=33
  210. puberté précoce --- r_associated #0: 33 --> en:dysmorphism
    n1=puberté précoce | n2=en:dysmorphism | rel=r_associated | relid=0 | w=33
  211. Sotos (syndrome de) --- r_associated #0: 32 --> en:dysmorphism
    n1=Sotos (syndrome de) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  212. dysplasie ectodermique, ectrodactylie et dystrophie maculaire --- r_associated #0: 32 --> en:dysmorphism
    n1=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  213. en:congenital abnormality of lower limb and/or pelvic girdle --- r_associated #0: 32 --> en:dysmorphism
    n1=en:congenital abnormality of lower limb and/or pelvic girdle | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  214. en:congenital deformity of knee joint --- r_associated #0: 32 --> en:dysmorphism
    n1=en:congenital deformity of knee joint | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  215. en:congenital failure of fusion --- r_associated #0: 32 --> en:dysmorphism
    n1=en:congenital failure of fusion | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  216. en:congenital malformation syndrome --- r_associated #0: 32 --> en:dysmorphism
    n1=en:congenital malformation syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  217. en:congenital urinary system abnormality --- r_associated #0: 32 --> en:dysmorphism
    n1=en:congenital urinary system abnormality | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  218. en:congenital vena cava abnormality --- r_associated #0: 32 --> en:dysmorphism
    n1=en:congenital vena cava abnormality | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  219. en:costello syndrome --- r_associated #0: 32 --> en:dysmorphism
    n1=en:costello syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  220. en:monster (disorder) --- r_associated #0: 32 --> en:dysmorphism
    n1=en:monster (disorder) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  221. en:other congenital anomalies of nervous system --- r_associated #0: 32 --> en:dysmorphism
    n1=en:other congenital anomalies of nervous system | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  222. en:other specified congenital malformations of face and neck --- r_associated #0: 32 --> en:dysmorphism
    n1=en:other specified congenital malformations of face and neck | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  223. en:phaces syndrome --- r_associated #0: 32 --> en:dysmorphism
    n1=en:phaces syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  224. en:sirenomelia --- r_associated #0: 32 --> en:dysmorphism
    n1=en:sirenomelia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  225. hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale --- r_associated #0: 32 --> en:dysmorphism
    n1=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  226. macroglossie --- r_associated #0: 32 --> en:dysmorphism
    n1=macroglossie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=32
  227. dysplasie ectodermique --- r_associated #0: 31 --> en:dysmorphism
    n1=dysplasie ectodermique | n2=en:dysmorphism | rel=r_associated | relid=0 | w=31
  228. dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental --- r_associated #0: 31 --> en:dysmorphism
    n1=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | n2=en:dysmorphism | rel=r_associated | relid=0 | w=31
  229. elliptocytose héréditaire --- r_associated #0: 31 --> en:dysmorphism
    n1=elliptocytose héréditaire | n2=en:dysmorphism | rel=r_associated | relid=0 | w=31
  230. en:cleft maxilla --- r_associated #0: 31 --> en:dysmorphism
    n1=en:cleft maxilla | n2=en:dysmorphism | rel=r_associated | relid=0 | w=31
  231. en:congenital abnormal fusion --- r_associated #0: 31 --> en:dysmorphism
    n1=en:congenital abnormal fusion | n2=en:dysmorphism | rel=r_associated | relid=0 | w=31
  232. en:congenital anomaly of face --- r_associated #0: 31 --> en:dysmorphism
    n1=en:congenital anomaly of face | n2=en:dysmorphism | rel=r_associated | relid=0 | w=31
  233. en:cranioschisis --- r_associated #0: 31 --> en:dysmorphism
    n1=en:cranioschisis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=31
  234. en:infection causing congenital anomaly --- r_associated #0: 31 --> en:dysmorphism
    n1=en:infection causing congenital anomaly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=31
  235. en:noonan syndrome --- r_associated #0: 31 --> en:dysmorphism
    n1=en:noonan syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=31
  236. en:ombilical hernia --- r_associated #0: 31 --> en:dysmorphism
    n1=en:ombilical hernia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=31
  237. en:trichorhinophalangeal syndrome --- r_associated #0: 31 --> en:dysmorphism
    n1=en:trichorhinophalangeal syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=31
  238. en:wildervanck's syndrome --- r_associated #0: 31 --> en:dysmorphism
    n1=en:wildervanck's syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=31
  239. oligophrénie --- r_associated #0: 31 --> en:dysmorphism
    n1=oligophrénie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=31
  240. anomalie du septum auriculaire --- r_associated #0: 30 --> en:dysmorphism
    n1=anomalie du septum auriculaire | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  241. arriération --- r_associated #0: 30 --> en:dysmorphism
    n1=arriération | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  242. déficience mentale --- r_associated #0: 30 --> en:dysmorphism
    n1=déficience mentale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  243. en:abnormalities, drug-induced --- r_associated #0: 30 --> en:dysmorphism
    n1=en:abnormalities, drug-induced | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  244. en:absent corpus callosum --- r_associated #0: 30 --> en:dysmorphism
    n1=en:absent corpus callosum | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  245. en:and mental retardation --- r_associated #0: 30 --> en:dysmorphism
    n1=en:and mental retardation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  246. en:atrial septal defect --- r_associated #0: 30 --> en:dysmorphism
    n1=en:atrial septal defect | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  247. en:bowen-conradi syndrome --- r_associated #0: 30 --> en:dysmorphism
    n1=en:bowen-conradi syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  248. en:cleft lip and palate --- r_associated #0: 30 --> en:dysmorphism
    n1=en:cleft lip and palate | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  249. en:congenital foot deformity --- r_associated #0: 30 --> en:dysmorphism
    n1=en:congenital foot deformity | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  250. en:developmental fault --- r_associated #0: 30 --> en:dysmorphism
    n1=en:developmental fault | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  251. en:exstrophy --- r_associated #0: 30 --> en:dysmorphism
    n1=en:exstrophy | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  252. en:hand and foot deformity --- r_associated #0: 30 --> en:dysmorphism
    n1=en:hand and foot deformity | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  253. en:learning disability --- r_associated #0: 30 --> en:dysmorphism
    n1=en:learning disability | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  254. en:mental handicap --- r_associated #0: 30 --> en:dysmorphism
    n1=en:mental handicap | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  255. en:nystagmus --- r_associated #0: 30 --> en:dysmorphism
    n1=en:nystagmus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  256. en:other congenital malformations of digestive system --- r_associated #0: 30 --> en:dysmorphism
    n1=en:other congenital malformations of digestive system | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  257. en:proctatresia --- r_associated #0: 30 --> en:dysmorphism
    n1=en:proctatresia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  258. en:retardation --- r_associated #0: 30 --> en:dysmorphism
    n1=en:retardation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  259. en:with growth retardation --- r_associated #0: 30 --> en:dysmorphism
    n1=en:with growth retardation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  260. exstrophie --- r_associated #0: 30 --> en:dysmorphism
    n1=exstrophie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  261. jumeaux conjoints --- r_associated #0: 30 --> en:dysmorphism
    n1=jumeaux conjoints | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
  262. contractures congénitales et arachnodactylie --- r_associated #0: 29 --> en:dysmorphism
    n1=contractures congénitales et arachnodactylie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  263. en:X-linked --- r_associated #0: 29 --> en:dysmorphism
    n1=en:X-linked | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  264. en:aplasia, nos --- r_associated #0: 29 --> en:dysmorphism
    n1=en:aplasia, nos | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  265. en:cleft palate with cleft lip --- r_associated #0: 29 --> en:dysmorphism
    n1=en:cleft palate with cleft lip | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  266. en:congenital anomaly of joint --- r_associated #0: 29 --> en:dysmorphism
    n1=en:congenital anomaly of joint | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  267. en:congenital hypoplasia of genital tubercle --- r_associated #0: 29 --> en:dysmorphism
    n1=en:congenital hypoplasia of genital tubercle | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  268. en:congenital musculoskeletal defect --- r_associated #0: 29 --> en:dysmorphism
    n1=en:congenital musculoskeletal defect | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  269. en:cryptophthalmia --- r_associated #0: 29 --> en:dysmorphism
    n1=en:cryptophthalmia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  270. en:developmental anomaly --- r_associated #0: 29 --> en:dysmorphism
    n1=en:developmental anomaly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  271. en:faciodigitogenital dysplasia --- r_associated #0: 29 --> en:dysmorphism
    n1=en:faciodigitogenital dysplasia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  272. en:feeble-mindedness --- r_associated #0: 29 --> en:dysmorphism
    n1=en:feeble-mindedness | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  273. en:hematomphalus --- r_associated #0: 29 --> en:dysmorphism
    n1=en:hematomphalus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  274. en:hypopituitarism --- r_associated #0: 29 --> en:dysmorphism
    n1=en:hypopituitarism | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  275. en:known or suspected fetal abnormality affecting management of mother --- r_associated #0: 29 --> en:dysmorphism
    n1=en:known or suspected fetal abnormality affecting management of mother | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  276. en:lymphatic abnormalities --- r_associated #0: 29 --> en:dysmorphism
    n1=en:lymphatic abnormalities | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  277. en:mental dullness --- r_associated #0: 29 --> en:dysmorphism
    n1=en:mental dullness | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  278. en:other specified congenital malformations --- r_associated #0: 29 --> en:dysmorphism
    n1=en:other specified congenital malformations | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  279. jumeaux fusionnés --- r_associated #0: 29 --> en:dysmorphism
    n1=jumeaux fusionnés | n2=en:dysmorphism | rel=r_associated | relid=0 | w=29
  280. brides amniotiques (syndrome des) --- r_associated #0: 28 --> en:dysmorphism
    n1=brides amniotiques (syndrome des) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  281. colobome de l'iris avec ptosis, hypertélorisme et retard mental --- r_associated #0: 28 --> en:dysmorphism
    n1=colobome de l'iris avec ptosis, hypertélorisme et retard mental | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  282. en:aase syndrome --- r_associated #0: 28 --> en:dysmorphism
    n1=en:aase syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  283. en:caudal dysplasia --- r_associated #0: 28 --> en:dysmorphism
    n1=en:caudal dysplasia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  284. en:cerebellar atrophy --- r_associated #0: 28 --> en:dysmorphism
    n1=en:cerebellar atrophy | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  285. en:ear, face and neck congenital anomalies --- r_associated #0: 28 --> en:dysmorphism
    n1=en:ear, face and neck congenital anomalies | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  286. en:ellis-van creveld syndrome --- r_associated #0: 28 --> en:dysmorphism
    n1=en:ellis-van creveld syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  287. en:exumbilication --- r_associated #0: 28 --> en:dysmorphism
    n1=en:exumbilication | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  288. en:fetal postural deformity --- r_associated #0: 28 --> en:dysmorphism
    n1=en:fetal postural deformity | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  289. en:kabuki syndrome --- r_associated #0: 28 --> en:dysmorphism
    n1=en:kabuki syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  290. en:kbg syndrome --- r_associated #0: 28 --> en:dysmorphism
    n1=en:kbg syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  291. en:neural tube defect --- r_associated #0: 28 --> en:dysmorphism
    n1=en:neural tube defect | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  292. en:nicolaides baraitser syndrome --- r_associated #0: 28 --> en:dysmorphism
    n1=en:nicolaides baraitser syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  293. en:oculo-dento-digital syndrome --- r_associated #0: 28 --> en:dysmorphism
    n1=en:oculo-dento-digital syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  294. en:oligophrenia --- r_associated #0: 28 --> en:dysmorphism
    n1=en:oligophrenia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  295. en:oligopsychia --- r_associated #0: 28 --> en:dysmorphism
    n1=en:oligopsychia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  296. en:other and unspecified congenital anomalies --- r_associated #0: 28 --> en:dysmorphism
    n1=en:other and unspecified congenital anomalies | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  297. en:radiation-induced disorder --- r_associated #0: 28 --> en:dysmorphism
    n1=en:radiation-induced disorder | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  298. en:transposition of great vessels --- r_associated #0: 28 --> en:dysmorphism
    n1=en:transposition of great vessels | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  299. en:umbilical hiatus --- r_associated #0: 28 --> en:dysmorphism
    n1=en:umbilical hiatus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  300. microdélétion 5q35 --- r_associated #0: 28 --> en:dysmorphism
    n1=microdélétion 5q35 | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  301. situs mutatus --- r_associated #0: 28 --> en:dysmorphism
    n1=situs mutatus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  302. troubles endocriniens, épilepsie et déficience mentale --- r_associated #0: 28 --> en:dysmorphism
    n1=troubles endocriniens, épilepsie et déficience mentale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=28
  303. albinisme oculocutané de type mutant jaune --- r_associated #0: 27 --> en:dysmorphism
    n1=albinisme oculocutané de type mutant jaune | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  304. cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie --- r_associated #0: 27 --> en:dysmorphism
    n1=cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  305. en:anal imperforation --- r_associated #0: 27 --> en:dysmorphism
    n1=en:anal imperforation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  306. en:caroli disease --- r_associated #0: 27 --> en:dysmorphism
    n1=en:caroli disease | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  307. en:congenital dysplasia --- r_associated #0: 27 --> en:dysmorphism
    n1=en:congenital dysplasia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  308. en:congenital malformation syndrome related to known exogenous cause --- r_associated #0: 27 --> en:dysmorphism
    n1=en:congenital malformation syndrome related to known exogenous cause | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  309. en:congenital stenosis --- r_associated #0: 27 --> en:dysmorphism
    n1=en:congenital stenosis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  310. en:congenital systemic disorder --- r_associated #0: 27 --> en:dysmorphism
    n1=en:congenital systemic disorder | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  311. en:delayed epiphyseal fusion --- r_associated #0: 27 --> en:dysmorphism
    n1=en:delayed epiphyseal fusion | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  312. en:epiphyseal dysplasia dysmorphism camptodactyly --- r_associated #0: 27 --> en:dysmorphism
    n1=en:epiphyseal dysplasia dysmorphism camptodactyly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  313. en:epiphyseal dysplasia hearing loss dysmorphism --- r_associated #0: 27 --> en:dysmorphism
    n1=en:epiphyseal dysplasia hearing loss dysmorphism | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  314. en:hypothalamic hamartoblastoma --- r_associated #0: 27 --> en:dysmorphism
    n1=en:hypothalamic hamartoblastoma | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  315. en:lowry wood syndrome --- r_associated #0: 27 --> en:dysmorphism
    n1=en:lowry wood syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  316. en:megaloglossia --- r_associated #0: 27 --> en:dysmorphism
    n1=en:megaloglossia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  317. en:smooth philtrum --- r_associated #0: 27 --> en:dysmorphism
    n1=en:smooth philtrum | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  318. en:thoracoschisis --- r_associated #0: 27 --> en:dysmorphism
    n1=en:thoracoschisis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=27
  319. dysmorphie --- r_associated #0: 26 --> en:dysmorphism
    n1=dysmorphie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=26
  320. en:certain congenital musculoskeletal deformities --- r_associated #0: 26 --> en:dysmorphism
    n1=en:certain congenital musculoskeletal deformities | n2=en:dysmorphism | rel=r_associated | relid=0 | w=26
  321. en:chromosomal aberration --- r_associated #0: 26 --> en:dysmorphism
    n1=en:chromosomal aberration | n2=en:dysmorphism | rel=r_associated | relid=0 | w=26
  322. en:cohen syndrome --- r_associated #0: 26 --> en:dysmorphism
    n1=en:cohen syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=26
  323. en:congenital extension deformity --- r_associated #0: 26 --> en:dysmorphism
    n1=en:congenital extension deformity | n2=en:dysmorphism | rel=r_associated | relid=0 | w=26
  324. en:congenital nervous system disorder --- r_associated #0: 26 --> en:dysmorphism
    n1=en:congenital nervous system disorder | n2=en:dysmorphism | rel=r_associated | relid=0 | w=26
  325. en:kosaki overgrowth syndrome --- r_associated #0: 26 --> en:dysmorphism
    n1=en:kosaki overgrowth syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=26
  326. en:limb deformities, congenital --- r_associated #0: 26 --> en:dysmorphism
    n1=en:limb deformities, congenital | n2=en:dysmorphism | rel=r_associated | relid=0 | w=26
  327. en:oligergasia --- r_associated #0: 26 --> en:dysmorphism
    n1=en:oligergasia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=26
  328. en:persistent cloaca --- r_associated #0: 26 --> en:dysmorphism
    n1=en:persistent cloaca | n2=en:dysmorphism | rel=r_associated | relid=0 | w=26
  329. en:strabismus syndrome --- r_associated #0: 26 --> en:dysmorphism
    n1=en:strabismus syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=26
  330. jumeaux siamois --- r_associated #0: 26 --> en:dysmorphism
    n1=jumeaux siamois | n2=en:dysmorphism | rel=r_associated | relid=0 | w=26
  331. malformation --- r_associated #0: 26 --> en:dysmorphism
    n1=malformation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=26
  332. phacomatose congenitale --- r_associated #0: 26 --> en:dysmorphism
    n1=phacomatose congenitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=26
  333. Déficience intellectuelle --- r_associated #0: 25 --> en:dysmorphism
    n1=Déficience intellectuelle | n2=en:dysmorphism | rel=r_associated | relid=0 | w=25
  334. albinisme avec pigmentation minime --- r_associated #0: 25 --> en:dysmorphism
    n1=albinisme avec pigmentation minime | n2=en:dysmorphism | rel=r_associated | relid=0 | w=25
  335. communication interventriculaire --- r_associated #0: 25 --> en:dysmorphism
    n1=communication interventriculaire | n2=en:dysmorphism | rel=r_associated | relid=0 | w=25
  336. en:Siamese twins --- r_associated #0: 25 --> en:dysmorphism
    n1=en:Siamese twins | n2=en:dysmorphism | rel=r_associated | relid=0 | w=25
  337. en:acephalostomia --- r_associated #0: 25 --> en:dysmorphism
    n1=en:acephalostomia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=25
  338. en:cheilognathoschisis --- r_associated #0: 25 --> en:dysmorphism
    n1=en:cheilognathoschisis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=25
  339. en:diaphragmatic hernia --- r_associated #0: 25 --> en:dysmorphism
    n1=en:diaphragmatic hernia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=25
  340. en:dysmorphosis --- r_associated #0: 25 --> en:dysmorphism
    n1=en:dysmorphosis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=25
  341. en:juvenile cataract --- r_associated #0: 25 --> en:dysmorphism
    n1=en:juvenile cataract | n2=en:dysmorphism | rel=r_associated | relid=0 | w=25
  342. en:monopia --- r_associated #0: 25 --> en:dysmorphism
    n1=en:monopia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=25
  343. frères siamois --- r_associated #0: 25 --> en:dysmorphism
    n1=frères siamois | n2=en:dysmorphism | rel=r_associated | relid=0 | w=25
  344. une anomalie congénitale --- r_associated #0: 25 --> en:dysmorphism
    n1=une anomalie congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=25
  345. cataracte-atrophie du cervelet-myopathie --- r_associated #0: 24 --> en:dysmorphism
    n1=cataracte-atrophie du cervelet-myopathie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=24
  346. cranioschisis --- r_associated #0: 24 --> en:dysmorphism
    n1=cranioschisis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=24
  347. en:amyoplasia congenita --- r_associated #0: 24 --> en:dysmorphism
    n1=en:amyoplasia congenita | n2=en:dysmorphism | rel=r_associated | relid=0 | w=24
  348. en:and microgenitalism --- r_associated #0: 24 --> en:dysmorphism
    n1=en:and microgenitalism | n2=en:dysmorphism | rel=r_associated | relid=0 | w=24
  349. en:deafness --- r_associated #0: 24 --> en:dysmorphism
    n1=en:deafness | n2=en:dysmorphism | rel=r_associated | relid=0 | w=24
  350. en:heart ectopy --- r_associated #0: 24 --> en:dysmorphism
    n1=en:heart ectopy | n2=en:dysmorphism | rel=r_associated | relid=0 | w=24
  351. syndrome hétérotaxique --- r_associated #0: 24 --> en:dysmorphism
    n1=syndrome hétérotaxique | n2=en:dysmorphism | rel=r_associated | relid=0 | w=24
  352. albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception --- r_associated #0: 23 --> en:dysmorphism
    n1=albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception | n2=en:dysmorphism | rel=r_associated | relid=0 | w=23
  353. en:Laron syndrome --- r_associated #0: 23 --> en:dysmorphism
    n1=en:Laron syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=23
  354. maladie de roger --- r_associated #0: 23 --> en:dysmorphism
    n1=maladie de roger | n2=en:dysmorphism | rel=r_associated | relid=0 | w=23
  355. télécanthus --- r_associated #0: 23 --> en:dysmorphism
    n1=télécanthus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=23
  356. en:dwarfism --- r_associated #0: 22 --> en:dysmorphism
    n1=en:dwarfism | n2=en:dysmorphism | rel=r_associated | relid=0 | w=22
  357. en:dysmorphy --- r_associated #0: 22 --> en:dysmorphism
    n1=en:dysmorphy | n2=en:dysmorphism | rel=r_associated | relid=0 | w=22
  358. en:morosis --- r_associated #0: 22 --> en:dysmorphism
    n1=en:morosis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=22
  359. en:onychoosteodysostosis --- r_associated #0: 22 --> en:dysmorphism
    n1=en:onychoosteodysostosis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=22
  360. en:craniostenosis --- r_associated #0: 21 --> en:dysmorphism
    n1=en:craniostenosis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=21
  361. hypopituitarisme --- r_associated #0: 21 --> en:dysmorphism
    n1=hypopituitarisme | n2=en:dysmorphism | rel=r_associated | relid=0 | w=21
  362. situs inversus viscerum --- r_associated #0: 21 --> en:dysmorphism
    n1=situs inversus viscerum | n2=en:dysmorphism | rel=r_associated | relid=0 | w=21
  363. ARTHROGRYPOSE --- r_associated #0: 20 --> en:dysmorphism
    n1=ARTHROGRYPOSE | n2=en:dysmorphism | rel=r_associated | relid=0 | w=20
  364. Malformation cardiaque --- r_associated #0: 20 --> en:dysmorphism
    n1=Malformation cardiaque | n2=en:dysmorphism | rel=r_associated | relid=0 | w=20
  365. en:anomaly congenital special senses --- r_associated #0: 20 --> en:dysmorphism
    n1=en:anomaly congenital special senses | n2=en:dysmorphism | rel=r_associated | relid=0 | w=20
  366. en:biliary atresia --- r_associated #0: 20 --> en:dysmorphism
    n1=en:biliary atresia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=20
  367. en:classical phenylketonuria --- r_associated #0: 20 --> en:dysmorphism
    n1=en:classical phenylketonuria | n2=en:dysmorphism | rel=r_associated | relid=0 | w=20
  368. en:cleft palate --- r_associated #0: 20 --> en:dysmorphism
    n1=en:cleft palate | n2=en:dysmorphism | rel=r_associated | relid=0 | w=20
  369. en:congenital anomaly of central nervous system --- r_associated #0: 20 --> en:dysmorphism
    n1=en:congenital anomaly of central nervous system | n2=en:dysmorphism | rel=r_associated | relid=0 | w=20
  370. en:congenital anomaly of gastrointestinal tract --- r_associated #0: 20 --> en:dysmorphism
    n1=en:congenital anomaly of gastrointestinal tract | n2=en:dysmorphism | rel=r_associated | relid=0 | w=20
  371. en:congenital genitourinary abnormality --- r_associated #0: 20 --> en:dysmorphism
    n1=en:congenital genitourinary abnormality | n2=en:dysmorphism | rel=r_associated | relid=0 | w=20
  372. en:congenital malformation of face and neck, unspecified --- r_associated #0: 20 --> en:dysmorphism
    n1=en:congenital malformation of face and neck, unspecified | n2=en:dysmorphism | rel=r_associated | relid=0 | w=20
  373. en:congenital morphologic anomaly --- r_associated #0: 20 --> en:dysmorphism
    n1=en:congenital morphologic anomaly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=20
  374. en:congenital respiratory system disorder --- r_associated #0: 20 --> en:dysmorphism
    n1=en:congenital respiratory system disorder | n2=en:dysmorphism | rel=r_associated | relid=0 | w=20
  375. en:connatal disorder --- r_associated #0: 20 --> en:dysmorphism
    n1=en:connatal disorder | n2=en:dysmorphism | rel=r_associated | relid=0 | w=20
  376. Albert (position d') --- r_associated #0: 15 --> en:dysmorphism
    n1=Albert (position d') | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  377. Anitschkow (cellule de) --- r_associated #0: 15 --> en:dysmorphism
    n1=Anitschkow (cellule de) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  378. Arrhenius (loi d') --- r_associated #0: 15 --> en:dysmorphism
    n1=Arrhenius (loi d') | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  379. Arthrogrypose --- r_associated #0: 15 --> en:dysmorphism
    n1=Arthrogrypose | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  380. CARD --- r_associated #0: 15 --> en:dysmorphism
    n1=CARD | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  381. Elliott (lambeau d') --- r_associated #0: 15 --> en:dysmorphism
    n1=Elliott (lambeau d') | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  382. Giessen (test de) --- r_associated #0: 15 --> en:dysmorphism
    n1=Giessen (test de) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  383. Maladies cardiaques --- r_associated #0: 15 --> en:dysmorphism
    n1=Maladies cardiaques | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  384. Malformation congénitale --- r_associated #0: 15 --> en:dysmorphism
    n1=Malformation congénitale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  385. cyclope (oeil) --- r_associated #0: 15 --> en:dysmorphism
    n1=cyclope (oeil) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  386. ectodermitis erosiva pluriorificialis --- r_associated #0: 15 --> en:dysmorphism
    n1=ectodermitis erosiva pluriorificialis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  387. ectodermose --- r_associated #0: 15 --> en:dysmorphism
    n1=ectodermose | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  388. ectodermose érosive pluriorificielle de Fiessinger-Rendu --- r_associated #0: 15 --> en:dysmorphism
    n1=ectodermose érosive pluriorificielle de Fiessinger-Rendu | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  389. ectoenzyme --- r_associated #0: 15 --> en:dysmorphism
    n1=ectoenzyme | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  390. ectomie --- r_associated #0: 15 --> en:dysmorphism
    n1=ectomie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  391. ectomorphie --- r_associated #0: 15 --> en:dysmorphism
    n1=ectomorphie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  392. ectoparasite --- r_associated #0: 15 --> en:dysmorphism
    n1=ectoparasite | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  393. ectoparasitose --- r_associated #0: 15 --> en:dysmorphism
    n1=ectoparasitose | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  394. exécutives (fonctions) --- r_associated #0: 15 --> en:dysmorphism
    n1=exécutives (fonctions) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  395. handicap mental --- r_associated #0: 15 --> en:dysmorphism
    n1=handicap mental | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  396. hydrocèle (cure chirurgicale d') --- r_associated #0: 15 --> en:dysmorphism
    n1=hydrocèle (cure chirurgicale d') | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  397. malentendant (enfant) --- r_associated #0: 15 --> en:dysmorphism
    n1=malentendant (enfant) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=15
  398. Albinisme --- r_associated #0: 10 --> en:dysmorphism
    n1=Albinisme | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  399. Anomalie chromosomique --- r_associated #0: 10 --> en:dysmorphism
    n1=Anomalie chromosomique | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  400. CONGÉNITALE --- r_associated #0: 10 --> en:dysmorphism
    n1=CONGÉNITALE | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  401. Card --- r_associated #0: 10 --> en:dysmorphism
    n1=Card | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  402. Cardiopathie --- r_associated #0: 10 --> en:dysmorphism
    n1=Cardiopathie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  403. Communication interauriculaire --- r_associated #0: 10 --> en:dysmorphism
    n1=Communication interauriculaire | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  404. Craniosynostose --- r_associated #0: 10 --> en:dysmorphism
    n1=Craniosynostose | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  405. Dysmorphie --- r_associated #0: 10 --> en:dysmorphism
    n1=Dysmorphie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  406. Déficience mentale --- r_associated #0: 10 --> en:dysmorphism
    n1=Déficience mentale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  407. Ectoparasite --- r_associated #0: 10 --> en:dysmorphism
    n1=Ectoparasite | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  408. Haltia-Santavuori (maladie de) --- r_associated #0: 10 --> en:dysmorphism
    n1=Haltia-Santavuori (maladie de) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  409. Hernie ombilicale --- r_associated #0: 10 --> en:dysmorphism
    n1=Hernie ombilicale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  410. Hydrocéphalie --- r_associated #0: 10 --> en:dysmorphism
    n1=Hydrocéphalie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  411. Hypertélorisme --- r_associated #0: 10 --> en:dysmorphism
    n1=Hypertélorisme | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  412. Hypoplasie --- r_associated #0: 10 --> en:dysmorphism
    n1=Hypoplasie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  413. Jumeaux siamois --- r_associated #0: 10 --> en:dysmorphism
    n1=Jumeaux siamois | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  414. Macroglossie --- r_associated #0: 10 --> en:dysmorphism
    n1=Macroglossie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  415. Malformation --- r_associated #0: 10 --> en:dysmorphism
    n1=Malformation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  416. Roger (maladie de) --- r_associated #0: 10 --> en:dysmorphism
    n1=Roger (maladie de) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  417. Sipple (syndrome de) --- r_associated #0: 10 --> en:dysmorphism
    n1=Sipple (syndrome de) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  418. Situs inversus --- r_associated #0: 10 --> en:dysmorphism
    n1=Situs inversus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  419. Syndrome de Sotos --- r_associated #0: 10 --> en:dysmorphism
    n1=Syndrome de Sotos | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  420. Völker-Dieben (atrophie optique liée au sexe de) --- r_associated #0: 10 --> en:dysmorphism
    n1=Völker-Dieben (atrophie optique liée au sexe de) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  421. Went (atrophie optique liée au sexe de) --- r_associated #0: 10 --> en:dysmorphism
    n1=Went (atrophie optique liée au sexe de) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  422. aberration chromosomique --- r_associated #0: 10 --> en:dysmorphism
    n1=aberration chromosomique | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  423. déficit intellectuel --- r_associated #0: 10 --> en:dysmorphism
    n1=déficit intellectuel | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  424. ectopie des procès ciliaires --- r_associated #0: 10 --> en:dysmorphism
    n1=ectopie des procès ciliaires | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  425. ectopie du cristallin --- r_associated #0: 10 --> en:dysmorphism
    n1=ectopie du cristallin | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  426. en:5q microdeletion --- r_associated #0: 10 --> en:dysmorphism
    n1=en:5q microdeletion | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  427. en:Albert's position --- r_associated #0: 10 --> en:dysmorphism
    n1=en:Albert's position | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  428. en:Anitschkow's cell --- r_associated #0: 10 --> en:dysmorphism
    n1=en:Anitschkow's cell | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  429. en:Arrhenius'law --- r_associated #0: 10 --> en:dysmorphism
    n1=en:Arrhenius'law | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  430. en:Elliott lateral flap --- r_associated #0: 10 --> en:dysmorphism
    n1=en:Elliott lateral flap | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  431. en:Siamese twin brothers --- r_associated #0: 10 --> en:dysmorphism
    n1=en:Siamese twin brothers | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  432. en:Sotos's syndrome --- r_associated #0: 10 --> en:dysmorphism
    n1=en:Sotos's syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  433. en:and growth retardation --- r_associated #0: 10 --> en:dysmorphism
    n1=en:and growth retardation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  434. en:and postaxil polydactylie --- r_associated #0: 10 --> en:dysmorphism
    n1=en:and postaxil polydactylie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  435. en:and sensorineural deafness --- r_associated #0: 10 --> en:dysmorphism
    n1=en:and sensorineural deafness | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  436. en:atresia ani --- r_associated #0: 10 --> en:dysmorphism
    n1=en:atresia ani | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  437. en:cacomorphosis --- r_associated #0: 10 --> en:dysmorphism
    n1=en:cacomorphosis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  438. en:chromosomal disorder --- r_associated #0: 10 --> en:dysmorphism
    n1=en:chromosomal disorder | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  439. en:conjoined twin brothers --- r_associated #0: 10 --> en:dysmorphism
    n1=en:conjoined twin brothers | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  440. en:conjoints twins --- r_associated #0: 10 --> en:dysmorphism
    n1=en:conjoints twins | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  441. en:contractural arachnodactyly --- r_associated #0: 10 --> en:dysmorphism
    n1=en:contractural arachnodactyly | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  442. en:coronary disease --- r_associated #0: 10 --> en:dysmorphism
    n1=en:coronary disease | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  443. en:cyclops eye --- r_associated #0: 10 --> en:dysmorphism
    n1=en:cyclops eye | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  444. en:ectodermosis --- r_associated #0: 10 --> en:dysmorphism
    n1=en:ectodermosis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  445. en:ectodermosis erosiva pluriorificialis --- r_associated #0: 10 --> en:dysmorphism
    n1=en:ectodermosis erosiva pluriorificialis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  446. en:ectoenzyme --- r_associated #0: 10 --> en:dysmorphism
    n1=en:ectoenzyme | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  447. en:ectoparasite --- r_associated #0: 10 --> en:dysmorphism
    n1=en:ectoparasite | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  448. en:ectoparasitosis --- r_associated #0: 10 --> en:dysmorphism
    n1=en:ectoparasitosis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  449. en:ectrodactyly and macular dystrophy --- r_associated #0: 10 --> en:dysmorphism
    n1=en:ectrodactyly and macular dystrophy | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  450. en:endocrine disorder --- r_associated #0: 10 --> en:dysmorphism
    n1=en:endocrine disorder | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  451. en:executive functions --- r_associated #0: 10 --> en:dysmorphism
    n1=en:executive functions | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  452. en:eye abnormality --- r_associated #0: 10 --> en:dysmorphism
    n1=en:eye abnormality | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  453. en:facial clefting syndrome --- r_associated #0: 10 --> en:dysmorphism
    n1=en:facial clefting syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  454. en:heart condition --- r_associated #0: 10 --> en:dysmorphism
    n1=en:heart condition | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  455. en:hypoacousic child --- r_associated #0: 10 --> en:dysmorphism
    n1=en:hypoacousic child | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  456. en:hypospadias --- r_associated #0: 10 --> en:dysmorphism
    n1=en:hypospadias | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  457. en:intellectual disability --- r_associated #0: 10 --> en:dysmorphism
    n1=en:intellectual disability | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  458. en:interatrial septal defect --- r_associated #0: 10 --> en:dysmorphism
    n1=en:interatrial septal defect | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  459. en:interventricular septal defect --- r_associated #0: 10 --> en:dysmorphism
    n1=en:interventricular septal defect | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  460. en:iris coloboma with ptosis --- r_associated #0: 10 --> en:dysmorphism
    n1=en:iris coloboma with ptosis | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  461. en:microtia --- r_associated #0: 10 --> en:dysmorphism
    n1=en:microtia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  462. en:minimal pigment type --- r_associated #0: 10 --> en:dysmorphism
    n1=en:minimal pigment type | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  463. en:myopia --- r_associated #0: 10 --> en:dysmorphism
    n1=en:myopia | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  464. en:polysyndactyly syndrome --- r_associated #0: 10 --> en:dysmorphism
    n1=en:polysyndactyly syndrome | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  465. en:secundum defect --- r_associated #0: 10 --> en:dysmorphism
    n1=en:secundum defect | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  466. en:sinus venosus defect --- r_associated #0: 10 --> en:dysmorphism
    n1=en:sinus venosus defect | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  467. en:surgical treatment of hydrocele --- r_associated #0: 10 --> en:dysmorphism
    n1=en:surgical treatment of hydrocele | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  468. en:unusual facies --- r_associated #0: 10 --> en:dysmorphism
    n1=en:unusual facies | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  469. en:water on the brain --- r_associated #0: 10 --> en:dysmorphism
    n1=en:water on the brain | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  470. faciale (paralysie du nouveau-né) --- r_associated #0: 10 --> en:dysmorphism
    n1=faciale (paralysie du nouveau-né) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  471. fente nasolabiopalatine --- r_associated #0: 10 --> en:dysmorphism
    n1=fente nasolabiopalatine | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  472. hernie diaphragmatique --- r_associated #0: 10 --> en:dysmorphism
    n1=hernie diaphragmatique | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  473. hydrocephalus --- r_associated #0: 10 --> en:dysmorphism
    n1=hydrocephalus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  474. hypertensinase --- r_associated #0: 10 --> en:dysmorphism
    n1=hypertensinase | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  475. hypertensine --- r_associated #0: 10 --> en:dysmorphism
    n1=hypertensine | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  476. hypertensinogène --- r_associated #0: 10 --> en:dysmorphism
    n1=hypertensinogène | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  477. hypertension --- r_associated #0: 10 --> en:dysmorphism
    n1=hypertension | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  478. hypertension abdominale --- r_associated #0: 10 --> en:dysmorphism
    n1=hypertension abdominale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  479. hypertension artérielle --- r_associated #0: 10 --> en:dysmorphism
    n1=hypertension artérielle | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  480. hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental --- r_associated #0: 10 --> en:dysmorphism
    n1=hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  481. hypohypophysie --- r_associated #0: 10 --> en:dysmorphism
    n1=hypohypophysie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  482. hypostimulinie --- r_associated #0: 10 --> en:dysmorphism
    n1=hypostimulinie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  483. impédance acoustique (symb. Z) --- r_associated #0: 10 --> en:dysmorphism
    n1=impédance acoustique (symb. Z) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  484. nanisme --- r_associated #0: 10 --> en:dysmorphism
    n1=nanisme | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  485. nanisme de type Laron --- r_associated #0: 10 --> en:dysmorphism
    n1=nanisme de type Laron | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  486. nystagmus --- r_associated #0: 10 --> en:dysmorphism
    n1=nystagmus | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  487. nystagmus héréditaire vertical --- r_associated #0: 10 --> en:dysmorphism
    n1=nystagmus héréditaire vertical | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  488. nystagmus lié au sexe --- r_associated #0: 10 --> en:dysmorphism
    n1=nystagmus lié au sexe | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  489. nystagmus myoclonies --- r_associated #0: 10 --> en:dysmorphism
    n1=nystagmus myoclonies | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  490. omovertébral (os) --- r_associated #0: 10 --> en:dysmorphism
    n1=omovertébral (os) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  491. quadriplégie spastique, rétinite pigmentaire et retard mental --- r_associated #0: 10 --> en:dysmorphism
    n1=quadriplégie spastique, rétinite pigmentaire et retard mental | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  492. rétinite pigmentaire et retard mental --- r_associated #0: 10 --> en:dysmorphism
    n1=rétinite pigmentaire et retard mental | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  493. rétinite pigmentaire, surdité, retard mental, et hypogonadisme --- r_associated #0: 10 --> en:dysmorphism
    n1=rétinite pigmentaire, surdité, retard mental, et hypogonadisme | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  494. souche de référence --- r_associated #0: 10 --> en:dysmorphism
    n1=souche de référence | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  495. souche transduite --- r_associated #0: 10 --> en:dysmorphism
    n1=souche transduite | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  496. surdité --- r_associated #0: 10 --> en:dysmorphism
    n1=surdité | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  497. syndrome cataracte-ataxie-surdité et retard mental --- r_associated #0: 10 --> en:dysmorphism
    n1=syndrome cataracte-ataxie-surdité et retard mental | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  498. syndrome de Treft-Sanborn-Carey --- r_associated #0: 10 --> en:dysmorphism
    n1=syndrome de Treft-Sanborn-Carey | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  499. trichomégalie avec retard mental, nanisme, et dégénérescence pigmentée de la rétine --- r_associated #0: 10 --> en:dysmorphism
    n1=trichomégalie avec retard mental, nanisme, et dégénérescence pigmentée de la rétine | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  500. télécardiographie --- r_associated #0: 10 --> en:dysmorphism
    n1=télécardiographie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  501. télécardiophone --- r_associated #0: 10 --> en:dysmorphism
    n1=télécardiophone | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  502. téléclitoridie --- r_associated #0: 10 --> en:dysmorphism
    n1=téléclitoridie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  503. télécobalt --- r_associated #0: 10 --> en:dysmorphism
    n1=télécobalt | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  504. télécobalt-thérapie --- r_associated #0: 10 --> en:dysmorphism
    n1=télécobalt-thérapie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  505. téléconsultation --- r_associated #0: 10 --> en:dysmorphism
    n1=téléconsultation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  506. télécrâne --- r_associated #0: 10 --> en:dysmorphism
    n1=télécrâne | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  507. télécæsiothérapie --- r_associated #0: 10 --> en:dysmorphism
    n1=télécæsiothérapie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  508. télédermatologie --- r_associated #0: 10 --> en:dysmorphism
    n1=télédermatologie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  509. télédiastole --- r_associated #0: 10 --> en:dysmorphism
    n1=télédiastole | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  510. télédétection --- r_associated #0: 10 --> en:dysmorphism
    n1=télédétection | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  511. urticaire-surdité-amylose rénale --- r_associated #0: 10 --> en:dysmorphism
    n1=urticaire-surdité-amylose rénale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  512. uréosecrétoire (constante) --- r_associated #0: 10 --> en:dysmorphism
    n1=uréosecrétoire (constante) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=10
  513. ANKRD11 gene --- r_associated #0: 5 --> en:dysmorphism
    n1=ANKRD11 gene | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  514. ARRX --- r_associated #0: 5 --> en:dysmorphism
    n1=ARRX | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  515. Exomphale --- r_associated #0: 5 --> en:dysmorphism
    n1=Exomphale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  516. Handicap mental --- r_associated #0: 5 --> en:dysmorphism
    n1=Handicap mental | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  517. Hypopituitarisme --- r_associated #0: 5 --> en:dysmorphism
    n1=Hypopituitarisme | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  518. Onsager (relation d') --- r_associated #0: 5 --> en:dysmorphism
    n1=Onsager (relation d') | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  519. albinisme avec immunodéficience et troubles hématologiques --- r_associated #0: 5 --> en:dysmorphism
    n1=albinisme avec immunodéficience et troubles hématologiques | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  520. albinisme avec surdité --- r_associated #0: 5 --> en:dysmorphism
    n1=albinisme avec surdité | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  521. ankyloblépharon --- r_associated #0: 5 --> en:dysmorphism
    n1=ankyloblépharon | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  522. ankyloblépharon filiforme et fente palatine --- r_associated #0: 5 --> en:dysmorphism
    n1=ankyloblépharon filiforme et fente palatine | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  523. ankyloblépharon, ongles hypoplasiques et cheveux bouclés --- r_associated #0: 5 --> en:dysmorphism
    n1=ankyloblépharon, ongles hypoplasiques et cheveux bouclés | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  524. ankyloblépharon-dysplasie ectodermique-fente labio-palatine --- r_associated #0: 5 --> en:dysmorphism
    n1=ankyloblépharon-dysplasie ectodermique-fente labio-palatine | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  525. arrière-pied --- r_associated #0: 5 --> en:dysmorphism
    n1=arrière-pied | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  526. cyclopeptide --- r_associated #0: 5 --> en:dysmorphism
    n1=cyclopeptide | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  527. cyclophiline --- r_associated #0: 5 --> en:dysmorphism
    n1=cyclophiline | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  528. cyclophorie --- r_associated #0: 5 --> en:dysmorphism
    n1=cyclophorie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  529. cyclophosphamide --- r_associated #0: 5 --> en:dysmorphism
    n1=cyclophosphamide | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  530. cyclophotocoagulation endoscopique --- r_associated #0: 5 --> en:dysmorphism
    n1=cyclophotocoagulation endoscopique | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  531. cyclophrénie --- r_associated #0: 5 --> en:dysmorphism
    n1=cyclophrénie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  532. cyclophyllidés --- r_associated #0: 5 --> en:dysmorphism
    n1=cyclophyllidés | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  533. ellipse d'engagement --- r_associated #0: 5 --> en:dysmorphism
    n1=ellipse d'engagement | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  534. ellipt.ocytose --- r_associated #0: 5 --> en:dysmorphism
    n1=ellipt.ocytose | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  535. elliptocyte --- r_associated #0: 5 --> en:dysmorphism
    n1=elliptocyte | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  536. elliptocytose --- r_associated #0: 5 --> en:dysmorphism
    n1=elliptocytose | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  537. exencéphale --- r_associated #0: 5 --> en:dysmorphism
    n1=exencéphale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  538. exénatide --- r_associated #0: 5 --> en:dysmorphism
    n1=exénatide | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  539. hydrocèle de la femme --- r_associated #0: 5 --> en:dysmorphism
    n1=hydrocèle de la femme | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  540. hydrocèle de la vaginale --- r_associated #0: 5 --> en:dysmorphism
    n1=hydrocèle de la vaginale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  541. hydrocèle du canal de Nück --- r_associated #0: 5 --> en:dysmorphism
    n1=hydrocèle du canal de Nück | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  542. hydrocèle du cou --- r_associated #0: 5 --> en:dysmorphism
    n1=hydrocèle du cou | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  543. malf ormation dysraphique --- r_associated #0: 5 --> en:dysmorphism
    n1=malf ormation dysraphique | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  544. malformation kystique adénomatoïde du poumon --- r_associated #0: 5 --> en:dysmorphism
    n1=malformation kystique adénomatoïde du poumon | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  545. malformation luxante de la hanche --- r_associated #0: 5 --> en:dysmorphism
    n1=malformation luxante de la hanche | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  546. malformation mamelonnaire --- r_associated #0: 5 --> en:dysmorphism
    n1=malformation mamelonnaire | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  547. malformation mammaire --- r_associated #0: 5 --> en:dysmorphism
    n1=malformation mammaire | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  548. malformation ombilicale --- r_associated #0: 5 --> en:dysmorphism
    n1=malformation ombilicale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  549. malformation utérine --- r_associated #0: 5 --> en:dysmorphism
    n1=malformation utérine | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  550. malformation vaginale --- r_associated #0: 5 --> en:dysmorphism
    n1=malformation vaginale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  551. malformation vasculaire cérébrale du nourrisson --- r_associated #0: 5 --> en:dysmorphism
    n1=malformation vasculaire cérébrale du nourrisson | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  552. malformations de la charnière occipitocervicale --- r_associated #0: 5 --> en:dysmorphism
    n1=malformations de la charnière occipitocervicale | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  553. nystagmus (zone de moindre) --- r_associated #0: 5 --> en:dysmorphism
    n1=nystagmus (zone de moindre) | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  554. onychodysplasie --- r_associated #0: 5 --> en:dysmorphism
    n1=onychodysplasie | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  555. onychogryphose --- r_associated #0: 5 --> en:dysmorphism
    n1=onychogryphose | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  556. onycholyse --- r_associated #0: 5 --> en:dysmorphism
    n1=onycholyse | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  557. onycholyse candidosique --- r_associated #0: 5 --> en:dysmorphism
    n1=onycholyse candidosique | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  558. onycholyse semi-lunaire partielle --- r_associated #0: 5 --> en:dysmorphism
    n1=onycholyse semi-lunaire partielle | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  559. onychomadèse --- r_associated #0: 5 --> en:dysmorphism
    n1=onychomadèse | n2=en:dysmorphism | rel=r_associated | relid=0 | w=5
  560. onychomatricome --- r_associated #0: 5 --> en:dysmorphism
    n1=onychomatricome | n2=en:dysmorphism | 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