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'en:harrod doman keele syndrome'
(id=6819197 ; fe=en:harrod doman keele syndrome ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=18186 creation date=2017-06-25 touchdate=2026-04-24 11:05:06.000)
≈ 288 relations sortantes

  1. en:harrod doman keele syndrome -- r_associated #0: 43 / 1 -> en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment
    n1=en:harrod doman keele syndrome | n2=en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment | rel=r_associated | relid=0 | w=43
  2. en:harrod doman keele syndrome -- r_associated #0: 42 / 0.977 -> en:congenital
    n1=en:harrod doman keele syndrome | n2=en:congenital | rel=r_associated | relid=0 | w=42
  3. en:harrod doman keele syndrome -- r_associated #0: 42 / 0.977 -> en:perniola krajewska carnevale syndrome
    n1=en:harrod doman keele syndrome | n2=en:perniola krajewska carnevale syndrome | rel=r_associated | relid=0 | w=42
  4. en:harrod doman keele syndrome -- r_associated #0: 41 / 0.953 -> en:membranous cranial ossification, delayed
    n1=en:harrod doman keele syndrome | n2=en:membranous cranial ossification, delayed | rel=r_associated | relid=0 | w=41
  5. en:harrod doman keele syndrome -- r_associated #0: 41 / 0.953 -> en:microphthalmia, syndromic 4 (disorder)
    n1=en:harrod doman keele syndrome | n2=en:microphthalmia, syndromic 4 (disorder) | rel=r_associated | relid=0 | w=41
  6. en:harrod doman keele syndrome -- r_associated #0: 41 / 0.953 -> en:profound intellectual disabilities
    n1=en:harrod doman keele syndrome | n2=en:profound intellectual disabilities | rel=r_associated | relid=0 | w=41
  7. en:harrod doman keele syndrome -- r_associated #0: 40 / 0.93 -> en:congenital anomaly of jaw
    n1=en:harrod doman keele syndrome | n2=en:congenital anomaly of jaw | rel=r_associated | relid=0 | w=40
  8. en:harrod doman keele syndrome -- r_associated #0: 40 / 0.93 -> en:treacher collins syndrome
    n1=en:harrod doman keele syndrome | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=40
  9. en:harrod doman keele syndrome -- r_associated #0: 39 / 0.907 -> en:gurrieri sammito bellussi syndrome
    n1=en:harrod doman keele syndrome | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=39
  10. en:harrod doman keele syndrome -- r_associated #0: 38 / 0.884 -> en:mesonephric cyst
    n1=en:harrod doman keele syndrome | n2=en:mesonephric cyst | rel=r_associated | relid=0 | w=38
  11. en:harrod doman keele syndrome -- r_associated #0: 38 / 0.884 -> en:o/e - hands - arachnodactyly
    n1=en:harrod doman keele syndrome | n2=en:o/e - hands - arachnodactyly | rel=r_associated | relid=0 | w=38
  12. en:harrod doman keele syndrome -- r_associated #0: 37 / 0.86 -> en:goniodysgenesis-mental retardation-short stature syndrome
    n1=en:harrod doman keele syndrome | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=37
  13. en:harrod doman keele syndrome -- r_associated #0: 37 / 0.86 -> en:renpenning syndrome 1
    n1=en:harrod doman keele syndrome | n2=en:renpenning syndrome 1 | rel=r_associated | relid=0 | w=37
  14. en:harrod doman keele syndrome -- r_associated #0: 36 / 0.837 -> en:goldenhar syndrome
    n1=en:harrod doman keele syndrome | n2=en:goldenhar syndrome | rel=r_associated | relid=0 | w=36
  15. en:harrod doman keele syndrome -- r_associated #0: 36 / 0.837 -> en:klinefelter syndrome
    n1=en:harrod doman keele syndrome | n2=en:klinefelter syndrome | rel=r_associated | relid=0 | w=36
  16. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:coffin-siris syndrome
    n1=en:harrod doman keele syndrome | n2=en:coffin-siris syndrome | rel=r_associated | relid=0 | w=35
  17. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:congenital anomaly of face bones
    n1=en:harrod doman keele syndrome | n2=en:congenital anomaly of face bones | rel=r_associated | relid=0 | w=35
  18. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:de sanctis-cacchione syndrome
    n1=en:harrod doman keele syndrome | n2=en:de sanctis-cacchione syndrome | rel=r_associated | relid=0 | w=35
  19. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:exencephaly
    n1=en:harrod doman keele syndrome | n2=en:exencephaly | rel=r_associated | relid=0 | w=35
  20. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:fraxe intellectual disability syndrome
    n1=en:harrod doman keele syndrome | n2=en:fraxe intellectual disability syndrome | rel=r_associated | relid=0 | w=35
  21. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:gaucher disease
    n1=en:harrod doman keele syndrome | n2=en:gaucher disease | rel=r_associated | relid=0 | w=35
  22. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:grob's syndrome
    n1=en:harrod doman keele syndrome | n2=en:grob's syndrome | rel=r_associated | relid=0 | w=35
  23. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate
    n1=en:harrod doman keele syndrome | n2=en:growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate | rel=r_associated | relid=0 | w=35
  24. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:hypospadias
    n1=en:harrod doman keele syndrome | n2=en:hypospadias | rel=r_associated | relid=0 | w=35
  25. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:karandikar maria kamble syndrome
    n1=en:harrod doman keele syndrome | n2=en:karandikar maria kamble syndrome | rel=r_associated | relid=0 | w=35
  26. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:kaufman-mckusick syndrome
    n1=en:harrod doman keele syndrome | n2=en:kaufman-mckusick syndrome | rel=r_associated | relid=0 | w=35
  27. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:laurence-moon syndrome
    n1=en:harrod doman keele syndrome | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=35
  28. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:lesch-nyhan syndrome
    n1=en:harrod doman keele syndrome | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=35
  29. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:lissencephaly syndrome, norman-roberts type
    n1=en:harrod doman keele syndrome | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=35
  30. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:melnick-fraser syndrome
    n1=en:harrod doman keele syndrome | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=35
  31. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:persistent urogenital sinus
    n1=en:harrod doman keele syndrome | n2=en:persistent urogenital sinus | rel=r_associated | relid=0 | w=35
  32. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:rozin hertz goodman syndrome
    n1=en:harrod doman keele syndrome | n2=en:rozin hertz goodman syndrome | rel=r_associated | relid=0 | w=35
  33. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:streak gonad
    n1=en:harrod doman keele syndrome | n2=en:streak gonad | rel=r_associated | relid=0 | w=35
  34. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:syndromic orbital border hypoplasia
    n1=en:harrod doman keele syndrome | n2=en:syndromic orbital border hypoplasia | rel=r_associated | relid=0 | w=35
  35. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:undescended and ectopic testicle
    n1=en:harrod doman keele syndrome | n2=en:undescended and ectopic testicle | rel=r_associated | relid=0 | w=35
  36. en:harrod doman keele syndrome -- r_associated #0: 35 / 0.814 -> en:waardenburg syndrome
    n1=en:harrod doman keele syndrome | n2=en:waardenburg syndrome | rel=r_associated | relid=0 | w=35
  37. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:ambiguous genitalia
    n1=en:harrod doman keele syndrome | n2=en:ambiguous genitalia | rel=r_associated | relid=0 | w=34
  38. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:borjeson-forssman-lehmann syndrome
    n1=en:harrod doman keele syndrome | n2=en:borjeson-forssman-lehmann syndrome | rel=r_associated | relid=0 | w=34
  39. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:congenital abnormality
    n1=en:harrod doman keele syndrome | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=34
  40. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:cranio-orbito-ocular dysraphia syndrome
    n1=en:harrod doman keele syndrome | n2=en:cranio-orbito-ocular dysraphia syndrome | rel=r_associated | relid=0 | w=34
  41. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:craniofrontonasal dysplasia
    n1=en:harrod doman keele syndrome | n2=en:craniofrontonasal dysplasia | rel=r_associated | relid=0 | w=34
  42. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:duplication of external genitalia
    n1=en:harrod doman keele syndrome | n2=en:duplication of external genitalia | rel=r_associated | relid=0 | w=34
  43. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:frontonasal dysplasia sequence
    n1=en:harrod doman keele syndrome | n2=en:frontonasal dysplasia sequence | rel=r_associated | relid=0 | w=34
  44. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:hypospadias-mental retardation syndrome
    n1=en:harrod doman keele syndrome | n2=en:hypospadias-mental retardation syndrome | rel=r_associated | relid=0 | w=34
  45. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:indeterminate sex and pseudohermaphroditism
    n1=en:harrod doman keele syndrome | n2=en:indeterminate sex and pseudohermaphroditism | rel=r_associated | relid=0 | w=34
  46. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:localized congenital skull defect
    n1=en:harrod doman keele syndrome | n2=en:localized congenital skull defect | rel=r_associated | relid=0 | w=34
  47. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:marfanoid mental retardation syndrome
    n1=en:harrod doman keele syndrome | n2=en:marfanoid mental retardation syndrome | rel=r_associated | relid=0 | w=34
  48. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:mowat-wilson syndrome
    n1=en:harrod doman keele syndrome | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=34
  49. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:partington x-linked mental retardation syndrome
    n1=en:harrod doman keele syndrome | n2=en:partington x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=34
  50. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:rett syndrome
    n1=en:harrod doman keele syndrome | n2=en:rett syndrome | rel=r_associated | relid=0 | w=34
  51. en:harrod doman keele syndrome -- r_associated #0: 34 / 0.791 -> en:van der woude syndrome
    n1=en:harrod doman keele syndrome | n2=en:van der woude syndrome | rel=r_associated | relid=0 | w=34
  52. en:harrod doman keele syndrome -- r_associated #0: 32 / 0.744 -> en:chromosome 17, trisomy 17p
    n1=en:harrod doman keele syndrome | n2=en:chromosome 17, trisomy 17p | rel=r_associated | relid=0 | w=32
  53. en:harrod doman keele syndrome -- r_associated #0: 32 / 0.744 -> en:fragile x syndrome
    n1=en:harrod doman keele syndrome | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=32
  54. en:harrod doman keele syndrome -- r_associated #0: 32 / 0.744 -> en:fronto-naso-ethmoidal dysostosis
    n1=en:harrod doman keele syndrome | n2=en:fronto-naso-ethmoidal dysostosis | rel=r_associated | relid=0 | w=32
  55. en:harrod doman keele syndrome -- r_associated #0: 32 / 0.744 -> en:fryns macrocephaly
    n1=en:harrod doman keele syndrome | n2=en:fryns macrocephaly | rel=r_associated | relid=0 | w=32
  56. en:harrod doman keele syndrome -- r_associated #0: 32 / 0.744 -> en:hydatid cyst
    n1=en:harrod doman keele syndrome | n2=en:hydatid cyst | rel=r_associated | relid=0 | w=32
  57. en:harrod doman keele syndrome -- r_associated #0: 32 / 0.744 -> en:maple syrup urine disease
    n1=en:harrod doman keele syndrome | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=32
  58. en:harrod doman keele syndrome -- r_associated #0: 32 / 0.744 -> en:marshall syndrome
    n1=en:harrod doman keele syndrome | n2=en:marshall syndrome | rel=r_associated | relid=0 | w=32
  59. en:harrod doman keele syndrome -- r_associated #0: 32 / 0.744 -> en:mcdonough syndrome
    n1=en:harrod doman keele syndrome | n2=en:mcdonough syndrome | rel=r_associated | relid=0 | w=32
  60. en:harrod doman keele syndrome -- r_associated #0: 32 / 0.744 -> en:mild mental retardation
    n1=en:harrod doman keele syndrome | n2=en:mild mental retardation | rel=r_associated | relid=0 | w=32
  61. en:harrod doman keele syndrome -- r_associated #0: 32 / 0.744 -> en:moderate mental retardation (i.q. 35-49)
    n1=en:harrod doman keele syndrome | n2=en:moderate mental retardation (i.q. 35-49) | rel=r_associated | relid=0 | w=32
  62. en:harrod doman keele syndrome -- r_associated #0: 32 / 0.744 -> en:sonoda syndrome
    n1=en:harrod doman keele syndrome | n2=en:sonoda syndrome | rel=r_associated | relid=0 | w=32
  63. en:harrod doman keele syndrome -- r_associated #0: 32 / 0.744 -> en:unspecified mental retardation; other impairments of behaviour
    n1=en:harrod doman keele syndrome | n2=en:unspecified mental retardation; other impairments of behaviour | rel=r_associated | relid=0 | w=32
  64. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:congenital contractural arachnodactyly
    n1=en:harrod doman keele syndrome | n2=en:congenital contractural arachnodactyly | rel=r_associated | relid=0 | w=31
  65. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:crane-heise syndrome
    n1=en:harrod doman keele syndrome | n2=en:crane-heise syndrome | rel=r_associated | relid=0 | w=31
  66. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:cyclopia
    n1=en:harrod doman keele syndrome | n2=en:cyclopia | rel=r_associated | relid=0 | w=31
  67. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:cyst of embryonic remnant - male
    n1=en:harrod doman keele syndrome | n2=en:cyst of embryonic remnant - male | rel=r_associated | relid=0 | w=31
  68. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:deafness-craniofacial syndrome
    n1=en:harrod doman keele syndrome | n2=en:deafness-craniofacial syndrome | rel=r_associated | relid=0 | w=31
  69. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:gonadal dysgenesis
    n1=en:harrod doman keele syndrome | n2=en:gonadal dysgenesis | rel=r_associated | relid=0 | w=31
  70. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:homocystinuria
    n1=en:harrod doman keele syndrome | n2=en:homocystinuria | rel=r_associated | relid=0 | w=31
  71. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:hyperphosphatasia with mental retardation
    n1=en:harrod doman keele syndrome | n2=en:hyperphosphatasia with mental retardation | rel=r_associated | relid=0 | w=31
  72. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:ichthyosis--cheek--eyebrow syndrome
    n1=en:harrod doman keele syndrome | n2=en:ichthyosis--cheek--eyebrow syndrome | rel=r_associated | relid=0 | w=31
  73. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:kabuki syndrome
    n1=en:harrod doman keele syndrome | n2=en:kabuki syndrome | rel=r_associated | relid=0 | w=31
  74. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:pierre robin syndrome
    n1=en:harrod doman keele syndrome | n2=en:pierre robin syndrome | rel=r_associated | relid=0 | w=31
  75. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:savant syndrome
    n1=en:harrod doman keele syndrome | n2=en:savant syndrome | rel=r_associated | relid=0 | w=31
  76. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:severe mental retardation (i.q. 20-34)
    n1=en:harrod doman keele syndrome | n2=en:severe mental retardation (i.q. 20-34) | rel=r_associated | relid=0 | w=31
  77. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:shprintzen omphalocele syndrome
    n1=en:harrod doman keele syndrome | n2=en:shprintzen omphalocele syndrome | rel=r_associated | relid=0 | w=31
  78. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:unspecified anomaly of cervix, vagina, and external female genitalia
    n1=en:harrod doman keele syndrome | n2=en:unspecified anomaly of cervix, vagina, and external female genitalia | rel=r_associated | relid=0 | w=31
  79. en:harrod doman keele syndrome -- r_associated #0: 31 / 0.721 -> en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour
    n1=en:harrod doman keele syndrome | n2=en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour | rel=r_associated | relid=0 | w=31
  80. en:harrod doman keele syndrome -- r_associated #0: 30 / 0.698 -> en:abnormally long growth
    n1=en:harrod doman keele syndrome | n2=en:abnormally long growth | rel=r_associated | relid=0 | w=30
  81. en:harrod doman keele syndrome -- r_associated #0: 30 / 0.698 -> en:histidinemia
    n1=en:harrod doman keele syndrome | n2=en:histidinemia | rel=r_associated | relid=0 | w=30
  82. en:harrod doman keele syndrome -- r_associated #0: 30 / 0.698 -> en:maxillonasal dysplasia, binder type
    n1=en:harrod doman keele syndrome | n2=en:maxillonasal dysplasia, binder type | rel=r_associated | relid=0 | w=30
  83. en:harrod doman keele syndrome -- r_associated #0: 30 / 0.698 -> en:mehes syndrome
    n1=en:harrod doman keele syndrome | n2=en:mehes syndrome | rel=r_associated | relid=0 | w=30
  84. en:harrod doman keele syndrome -- r_associated #0: 30 / 0.698 -> en:multiple congenital anomalies
    n1=en:harrod doman keele syndrome | n2=en:multiple congenital anomalies | rel=r_associated | relid=0 | w=30
  85. en:harrod doman keele syndrome -- r_associated #0: 30 / 0.698 -> en:neuronal ceroid lipofuscinosis
    n1=en:harrod doman keele syndrome | n2=en:neuronal ceroid lipofuscinosis | rel=r_associated | relid=0 | w=30
  86. en:harrod doman keele syndrome -- r_associated #0: 30 / 0.698 -> en:oculocerebrorenal syndrome
    n1=en:harrod doman keele syndrome | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=30
  87. en:harrod doman keele syndrome -- r_associated #0: 30 / 0.698 -> en:opitz trigonocephaly syndrome
    n1=en:harrod doman keele syndrome | n2=en:opitz trigonocephaly syndrome | rel=r_associated | relid=0 | w=30
  88. en:harrod doman keele syndrome -- r_associated #0: 30 / 0.698 -> en:orotic aciduria
    n1=en:harrod doman keele syndrome | n2=en:orotic aciduria | rel=r_associated | relid=0 | w=30
  89. en:harrod doman keele syndrome -- r_associated #0: 30 / 0.698 -> en:undescended testes
    n1=en:harrod doman keele syndrome | n2=en:undescended testes | rel=r_associated | relid=0 | w=30
  90. en:harrod doman keele syndrome -- r_associated #0: 29 / 0.674 -> en:congenital anomaly of male genital system
    n1=en:harrod doman keele syndrome | n2=en:congenital anomaly of male genital system | rel=r_associated | relid=0 | w=29
  91. en:harrod doman keele syndrome -- r_associated #0: 29 / 0.674 -> en:de barsy syndrome
    n1=en:harrod doman keele syndrome | n2=en:de barsy syndrome | rel=r_associated | relid=0 | w=29
  92. en:harrod doman keele syndrome -- r_associated #0: 29 / 0.674 -> en:encephalocele
    n1=en:harrod doman keele syndrome | n2=en:encephalocele | rel=r_associated | relid=0 | w=29
  93. en:harrod doman keele syndrome -- r_associated #0: 29 / 0.674 -> en:fronto-facio-nasal dysplasia
    n1=en:harrod doman keele syndrome | n2=en:fronto-facio-nasal dysplasia | rel=r_associated | relid=0 | w=29
  94. en:harrod doman keele syndrome -- r_associated #0: 29 / 0.674 -> en:fryns syndrome
    n1=en:harrod doman keele syndrome | n2=en:fryns syndrome | rel=r_associated | relid=0 | w=29
  95. en:harrod doman keele syndrome -- r_associated #0: 29 / 0.674 -> en:hypospadias and epispadias and other penile anomalies
    n1=en:harrod doman keele syndrome | n2=en:hypospadias and epispadias and other penile anomalies | rel=r_associated | relid=0 | w=29
  96. en:harrod doman keele syndrome -- r_associated #0: 29 / 0.674 -> en:lujan fryns syndrome
    n1=en:harrod doman keele syndrome | n2=en:lujan fryns syndrome | rel=r_associated | relid=0 | w=29
  97. en:harrod doman keele syndrome -- r_associated #0: 29 / 0.674 -> en:other anomalies of uterus
    n1=en:harrod doman keele syndrome | n2=en:other anomalies of uterus | rel=r_associated | relid=0 | w=29
  98. en:harrod doman keele syndrome -- r_associated #0: 29 / 0.674 -> en:other specified anomalies of genital organs
    n1=en:harrod doman keele syndrome | n2=en:other specified anomalies of genital organs | rel=r_associated | relid=0 | w=29
  99. en:harrod doman keele syndrome -- r_associated #0: 29 / 0.674 -> en:pseudotrisomy 13 syndrome
    n1=en:harrod doman keele syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  100. en:harrod doman keele syndrome -- r_associated #0: 29 / 0.674 -> en:tuberous sclerosis
    n1=en:harrod doman keele syndrome | n2=en:tuberous sclerosis | rel=r_associated | relid=0 | w=29
  101. en:harrod doman keele syndrome -- r_associated #0: 29 / 0.674 -> en:unspecified mental retardation; without mention of impairment of behaviour
    n1=en:harrod doman keele syndrome | n2=en:unspecified mental retardation; without mention of impairment of behaviour | rel=r_associated | relid=0 | w=29
  102. en:harrod doman keele syndrome -- r_associated #0: 29 / 0.674 -> en:uterus bilocularis
    n1=en:harrod doman keele syndrome | n2=en:uterus bilocularis | rel=r_associated | relid=0 | w=29
  103. en:harrod doman keele syndrome -- r_associated #0: 29 / 0.674 -> en:wolf-hirschhorn syndrome
    n1=en:harrod doman keele syndrome | n2=en:wolf-hirschhorn syndrome | rel=r_associated | relid=0 | w=29
  104. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:bardet-biedl syndrome
    n1=en:harrod doman keele syndrome | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=28
  105. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:blepharophimosis syndrome ohdo type
    n1=en:harrod doman keele syndrome | n2=en:blepharophimosis syndrome ohdo type | rel=r_associated | relid=0 | w=28
  106. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:borderline mental retardation (i.q. 70-85)
    n1=en:harrod doman keele syndrome | n2=en:borderline mental retardation (i.q. 70-85) | rel=r_associated | relid=0 | w=28
  107. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:cask related intellectual disability
    n1=en:harrod doman keele syndrome | n2=en:cask related intellectual disability | rel=r_associated | relid=0 | w=28
  108. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:chromosome 17q21.31 deletion syndrome
    n1=en:harrod doman keele syndrome | n2=en:chromosome 17q21.31 deletion syndrome | rel=r_associated | relid=0 | w=28
  109. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:classical phenylketonuria
    n1=en:harrod doman keele syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28
  110. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:congenital anomaly of female genital system
    n1=en:harrod doman keele syndrome | n2=en:congenital anomaly of female genital system | rel=r_associated | relid=0 | w=28
  111. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:congenital anomaly of ovary
    n1=en:harrod doman keele syndrome | n2=en:congenital anomaly of ovary | rel=r_associated | relid=0 | w=28
  112. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:congenital anomaly of skull
    n1=en:harrod doman keele syndrome | n2=en:congenital anomaly of skull | rel=r_associated | relid=0 | w=28
  113. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:congenital malformations of ovaries, fallopian tubes and broad ligaments
    n1=en:harrod doman keele syndrome | n2=en:congenital malformations of ovaries, fallopian tubes and broad ligaments | rel=r_associated | relid=0 | w=28
  114. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:down syndrome
    n1=en:harrod doman keele syndrome | n2=en:down syndrome | rel=r_associated | relid=0 | w=28
  115. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:haspeslagh fryns muelenaere syndrome
    n1=en:harrod doman keele syndrome | n2=en:haspeslagh fryns muelenaere syndrome | rel=r_associated | relid=0 | w=28
  116. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:kohlschutter tonz syndrome
    n1=en:harrod doman keele syndrome | n2=en:kohlschutter tonz syndrome | rel=r_associated | relid=0 | w=28
  117. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:lubs x-linked mental retardation syndrome
    n1=en:harrod doman keele syndrome | n2=en:lubs x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=28
  118. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:mental retardation, x-linked, snyder-robinson type
    n1=en:harrod doman keele syndrome | n2=en:mental retardation, x-linked, snyder-robinson type | rel=r_associated | relid=0 | w=28
  119. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:microcephaly deafness syndrome
    n1=en:harrod doman keele syndrome | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=28
  120. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:other congenital malformations of female genitalia
    n1=en:harrod doman keele syndrome | n2=en:other congenital malformations of female genitalia | rel=r_associated | relid=0 | w=28
  121. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:spheno-frontal dysostosis
    n1=en:harrod doman keele syndrome | n2=en:spheno-frontal dysostosis | rel=r_associated | relid=0 | w=28
  122. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:undescended and retractile testicle
    n1=en:harrod doman keele syndrome | n2=en:undescended and retractile testicle | rel=r_associated | relid=0 | w=28
  123. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:waisman syndrome
    n1=en:harrod doman keele syndrome | n2=en:waisman syndrome | rel=r_associated | relid=0 | w=28
  124. en:harrod doman keele syndrome -- r_associated #0: 28 / 0.651 -> en:wildervanck's syndrome
    n1=en:harrod doman keele syndrome | n2=en:wildervanck's syndrome | rel=r_associated | relid=0 | w=28
  125. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:cleft lip sequence
    n1=en:harrod doman keele syndrome | n2=en:cleft lip sequence | rel=r_associated | relid=0 | w=27
  126. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:cyst of wolffian duct
    n1=en:harrod doman keele syndrome | n2=en:cyst of wolffian duct | rel=r_associated | relid=0 | w=27
  127. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:female restricted epilepsy with intellectual disability syndrome
    n1=en:harrod doman keele syndrome | n2=en:female restricted epilepsy with intellectual disability syndrome | rel=r_associated | relid=0 | w=27
  128. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:huntington's disease
    n1=en:harrod doman keele syndrome | n2=en:huntington's disease | rel=r_associated | relid=0 | w=27
  129. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:intellectual disability
    n1=en:harrod doman keele syndrome | n2=en:intellectual disability | rel=r_associated | relid=0 | w=27
  130. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:lissencephaly, x-linked, 2
    n1=en:harrod doman keele syndrome | n2=en:lissencephaly, x-linked, 2 | rel=r_associated | relid=0 | w=27
  131. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:masa syndrome (disorder)
    n1=en:harrod doman keele syndrome | n2=en:masa syndrome (disorder) | rel=r_associated | relid=0 | w=27
  132. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:morm syndrome
    n1=en:harrod doman keele syndrome | n2=en:morm syndrome | rel=r_associated | relid=0 | w=27
  133. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:multiple malformation syndrome with facial-limb defects as major feature
    n1=en:harrod doman keele syndrome | n2=en:multiple malformation syndrome with facial-limb defects as major feature | rel=r_associated | relid=0 | w=27
  134. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:nutritional mental retardation
    n1=en:harrod doman keele syndrome | n2=en:nutritional mental retardation | rel=r_associated | relid=0 | w=27
  135. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:otocephaly
    n1=en:harrod doman keele syndrome | n2=en:otocephaly | rel=r_associated | relid=0 | w=27
  136. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:prader-willi syndrome
    n1=en:harrod doman keele syndrome | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=27
  137. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:syndrome, branchio-oculo-facial
    n1=en:harrod doman keele syndrome | n2=en:syndrome, branchio-oculo-facial | rel=r_associated | relid=0 | w=27
  138. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:thomas syndrome
    n1=en:harrod doman keele syndrome | n2=en:thomas syndrome | rel=r_associated | relid=0 | w=27
  139. en:harrod doman keele syndrome -- r_associated #0: 27 / 0.628 -> en:wellesley carman french syndrome
    n1=en:harrod doman keele syndrome | n2=en:wellesley carman french syndrome | rel=r_associated | relid=0 | w=27
  140. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> en:acromelic frontonasal dysostosis
    n1=en:harrod doman keele syndrome | n2=en:acromelic frontonasal dysostosis | rel=r_associated | relid=0 | w=26
  141. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> en:angelman syndrome
    n1=en:harrod doman keele syndrome | n2=en:angelman syndrome | rel=r_associated | relid=0 | w=26
  142. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> en:blepharophimosis, ptosis, and epicanthus inversus (disorder)
    n1=en:harrod doman keele syndrome | n2=en:blepharophimosis, ptosis, and epicanthus inversus (disorder) | rel=r_associated | relid=0 | w=26
  143. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> en:cayler cardiofacial syndrome
    n1=en:harrod doman keele syndrome | n2=en:cayler cardiofacial syndrome | rel=r_associated | relid=0 | w=26
  144. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> en:char syndrome
    n1=en:harrod doman keele syndrome | n2=en:char syndrome | rel=r_associated | relid=0 | w=26
  145. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> en:congenital malformation of uterus and cervix
    n1=en:harrod doman keele syndrome | n2=en:congenital malformation of uterus and cervix | rel=r_associated | relid=0 | w=26
  146. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> en:craniofacial abnormalities
    n1=en:harrod doman keele syndrome | n2=en:craniofacial abnormalities | rel=r_associated | relid=0 | w=26
  147. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> en:fallopian tube and broad ligament anomalies
    n1=en:harrod doman keele syndrome | n2=en:fallopian tube and broad ligament anomalies | rel=r_associated | relid=0 | w=26
  148. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> en:fronto-frontal dysostosis
    n1=en:harrod doman keele syndrome | n2=en:fronto-frontal dysostosis | rel=r_associated | relid=0 | w=26
  149. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> en:myopathy, congenital nonprogressive with moebius and robin sequences
    n1=en:harrod doman keele syndrome | n2=en:myopathy, congenital nonprogressive with moebius and robin sequences | rel=r_associated | relid=0 | w=26
  150. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> en:other mental retardation
    n1=en:harrod doman keele syndrome | n2=en:other mental retardation | rel=r_associated | relid=0 | w=26
  151. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> en:prader-willi habitus, osteopenia, and camptodactyly
    n1=en:harrod doman keele syndrome | n2=en:prader-willi habitus, osteopenia, and camptodactyly | rel=r_associated | relid=0 | w=26
  152. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> en:smith-magenis syndrome
    n1=en:harrod doman keele syndrome | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=26
  153. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> en:trisomy 10p
    n1=en:harrod doman keele syndrome | n2=en:trisomy 10p | rel=r_associated | relid=0 | w=26
  154. en:harrod doman keele syndrome -- r_associated #0: 26 / 0.605 -> syndrome
    n1=en:harrod doman keele syndrome | n2=syndrome | rel=r_associated | relid=0 | w=26
  155. en:harrod doman keele syndrome -- r_associated #0: 22 / 0.512 -> anomalie congénitale
    n1=en:harrod doman keele syndrome | n2=anomalie congénitale | rel=r_associated | relid=0 | w=22
  156. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> anomalie du développement
    n1=en:harrod doman keele syndrome | n2=anomalie du développement | rel=r_associated | relid=0 | w=20
  157. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> arachnodactylie et contractures congénitales
    n1=en:harrod doman keele syndrome | n2=arachnodactylie et contractures congénitales | rel=r_associated | relid=0 | w=20
  158. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> cétoacidurie à chaînes ramifiées
    n1=en:harrod doman keele syndrome | n2=cétoacidurie à chaînes ramifiées | rel=r_associated | relid=0 | w=20
  159. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> Chopart (désarticulation de)
    n1=en:harrod doman keele syndrome | n2=Chopart (désarticulation de) | rel=r_associated | relid=0 | w=20
  160. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> Chorée
    n1=en:harrod doman keele syndrome | n2=Chorée | rel=r_associated | relid=0 | w=20
  161. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> chorée de Huntington
    n1=en:harrod doman keele syndrome | n2=chorée de Huntington | rel=r_associated | relid=0 | w=20
  162. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> chorée de huntington
    n1=en:harrod doman keele syndrome | n2=chorée de huntington | rel=r_associated | relid=0 | w=20
  163. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> chorée de saint jean
    n1=en:harrod doman keele syndrome | n2=chorée de saint jean | rel=r_associated | relid=0 | w=20
  164. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> chorée de Sydenham
    n1=en:harrod doman keele syndrome | n2=chorée de Sydenham | rel=r_associated | relid=0 | w=20
  165. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> chorée de sydenham
    n1=en:harrod doman keele syndrome | n2=chorée de sydenham | rel=r_associated | relid=0 | w=20
  166. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> chorée héréditaire
    n1=en:harrod doman keele syndrome | n2=chorée héréditaire | rel=r_associated | relid=0 | w=20
  167. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> chorée rhumatismale
    n1=en:harrod doman keele syndrome | n2=chorée rhumatismale | rel=r_associated | relid=0 | w=20
  168. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> chorée rhumatismale sans atteinte cardiaque
    n1=en:harrod doman keele syndrome | n2=chorée rhumatismale sans atteinte cardiaque | rel=r_associated | relid=0 | w=20
  169. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> chorées
    n1=en:harrod doman keele syndrome | n2=chorées | rel=r_associated | relid=0 | w=20
  170. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> congénital
    n1=en:harrod doman keele syndrome | n2=congénital | rel=r_associated | relid=0 | w=20
  171. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> congenital
    n1=en:harrod doman keele syndrome | n2=congenital | rel=r_associated | relid=0 | w=20
  172. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> congénitale
    n1=en:harrod doman keele syndrome | n2=congénitale | rel=r_associated | relid=0 | w=20
  173. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> cyclopia
    n1=en:harrod doman keele syndrome | n2=cyclopia | rel=r_associated | relid=0 | w=20
  174. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> cyclopie
    n1=en:harrod doman keele syndrome | n2=cyclopie | rel=r_associated | relid=0 | w=20
  175. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> danse de saint Guy
    n1=en:harrod doman keele syndrome | n2=danse de saint Guy | rel=r_associated | relid=0 | w=20
  176. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> déficience congénitale
    n1=en:harrod doman keele syndrome | n2=déficience congénitale | rel=r_associated | relid=0 | w=20
  177. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> déficit en céto-acide décarboxylase
    n1=en:harrod doman keele syndrome | n2=déficit en céto-acide décarboxylase | rel=r_associated | relid=0 | w=20
  178. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> déformation congénitale
    n1=en:harrod doman keele syndrome | n2=déformation congénitale | rel=r_associated | relid=0 | w=20
  179. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> difformité congénitale
    n1=en:harrod doman keele syndrome | n2=difformité congénitale | rel=r_associated | relid=0 | w=20
  180. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> dysostose fronto-nasale acromélique
    n1=en:harrod doman keele syndrome | n2=dysostose fronto-nasale acromélique | rel=r_associated | relid=0 | w=20
  181. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> dysplasie fronto-nasale acromélique
    n1=en:harrod doman keele syndrome | n2=dysplasie fronto-nasale acromélique | rel=r_associated | relid=0 | w=20
  182. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:12q14 microdeletion syndrome
    n1=en:harrod doman keele syndrome | n2=en:12q14 microdeletion syndrome | rel=r_associated | relid=0 | w=20
  183. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:17q11.2 microduplication syndrome
    n1=en:harrod doman keele syndrome | n2=en:17q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=20
  184. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:1p21.3 microdeletion syndrome
    n1=en:harrod doman keele syndrome | n2=en:1p21.3 microdeletion syndrome | rel=r_associated | relid=0 | w=20
  185. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:Angelman syndrome
    n1=en:harrod doman keele syndrome | n2=en:Angelman syndrome | rel=r_associated | relid=0 | w=20
  186. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:aniridia and intellectual disability syndrome
    n1=en:harrod doman keele syndrome | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=20
  187. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:arachnodactyly and intellectual disability with facial dysmorphism syndrome
    n1=en:harrod doman keele syndrome | n2=en:arachnodactyly and intellectual disability with facial dysmorphism syndrome | rel=r_associated | relid=0 | w=20
  188. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:arhinia, choanal atresia, and microphthalmia
    n1=en:harrod doman keele syndrome | n2=en:arhinia, choanal atresia, and microphthalmia | rel=r_associated | relid=0 | w=20
  189. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:birth defect
    n1=en:harrod doman keele syndrome | n2=en:birth defect | rel=r_associated | relid=0 | w=20
  190. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:brachioskeletogenital syndrome
    n1=en:harrod doman keele syndrome | n2=en:brachioskeletogenital syndrome | rel=r_associated | relid=0 | w=20
  191. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:branched-chain ketoaciduria
    n1=en:harrod doman keele syndrome | n2=en:branched-chain ketoaciduria | rel=r_associated | relid=0 | w=20
  192. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:classical maple syrup urine disease
    n1=en:harrod doman keele syndrome | n2=en:classical maple syrup urine disease | rel=r_associated | relid=0 | w=20
  193. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:congenital anomaly
    n1=en:harrod doman keele syndrome | n2=en:congenital anomaly | rel=r_associated | relid=0 | w=20
  194. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:congenital cataract with ataxia and deafness syndrome
    n1=en:harrod doman keele syndrome | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=20
  195. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:congenital defect
    n1=en:harrod doman keele syndrome | n2=en:congenital defect | rel=r_associated | relid=0 | w=20
  196. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:congenital malformation
    n1=en:harrod doman keele syndrome | n2=en:congenital malformation | rel=r_associated | relid=0 | w=20
  197. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:cooper jabs syndrome
    n1=en:harrod doman keele syndrome | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=20
  198. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
    n1=en:harrod doman keele syndrome | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=20
  199. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:developmental fault
    n1=en:harrod doman keele syndrome | n2=en:developmental fault | rel=r_associated | relid=0 | w=20
  200. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:Down syndrome
    n1=en:harrod doman keele syndrome | n2=en:Down syndrome | rel=r_associated | relid=0 | w=20
  201. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:dysmorphism, pectus carinatum, joint laxity syndrome
    n1=en:harrod doman keele syndrome | n2=en:dysmorphism, pectus carinatum, joint laxity syndrome | rel=r_associated | relid=0 | w=20
  202. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:echinococcus cyst
    n1=en:harrod doman keele syndrome | n2=en:echinococcus cyst | rel=r_associated | relid=0 | w=20
  203. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:ectodermal dysplasia with blindness syndrome
    n1=en:harrod doman keele syndrome | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20
  204. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:exenkephaly
    n1=en:harrod doman keele syndrome | n2=en:exenkephaly | rel=r_associated | relid=0 | w=20
  205. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:fara chlupackova syndrome
    n1=en:harrod doman keele syndrome | n2=en:fara chlupackova syndrome | rel=r_associated | relid=0 | w=20
  206. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:fountain syndrome
    n1=en:harrod doman keele syndrome | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=20
  207. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:fragile X syndrome
    n1=en:harrod doman keele syndrome | n2=en:fragile X syndrome | rel=r_associated | relid=0 | w=20
  208. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:fried syndrome
    n1=en:harrod doman keele syndrome | n2=en:fried syndrome | rel=r_associated | relid=0 | w=20
  209. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:Gaucher disease
    n1=en:harrod doman keele syndrome | n2=en:Gaucher disease | rel=r_associated | relid=0 | w=20
  210. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:halal syndrome
    n1=en:harrod doman keele syndrome | n2=en:halal syndrome | rel=r_associated | relid=0 | w=20
  211. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:hall riggs syndrome
    n1=en:harrod doman keele syndrome | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=20
  212. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:histidinaemia
    n1=en:harrod doman keele syndrome | n2=en:histidinaemia | rel=r_associated | relid=0 | w=20
  213. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:Huntington's disease
    n1=en:harrod doman keele syndrome | n2=en:Huntington's disease | rel=r_associated | relid=0 | w=20
  214. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:hydatic cyst
    n1=en:harrod doman keele syndrome | n2=en:hydatic cyst | rel=r_associated | relid=0 | w=20
  215. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:hypertrichosis and acromegaloid facial appearance syndrome
    n1=en:harrod doman keele syndrome | n2=en:hypertrichosis and acromegaloid facial appearance syndrome | rel=r_associated | relid=0 | w=20
  216. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:hypomandibular faciocranial dysostosis
    n1=en:harrod doman keele syndrome | n2=en:hypomandibular faciocranial dysostosis | rel=r_associated | relid=0 | w=20
  217. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:Klinefelter syndrome
    n1=en:harrod doman keele syndrome | n2=en:Klinefelter syndrome | rel=r_associated | relid=0 | w=20
  218. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:kosztolanyi syndrome
    n1=en:harrod doman keele syndrome | n2=en:kosztolanyi syndrome | rel=r_associated | relid=0 | w=20
  219. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:leucinosis
    n1=en:harrod doman keele syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  220. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:major physical defect
    n1=en:harrod doman keele syndrome | n2=en:major physical defect | rel=r_associated | relid=0 | w=20
  221. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:maple-tree syrup disease
    n1=en:harrod doman keele syndrome | n2=en:maple-tree syrup disease | rel=r_associated | relid=0 | w=20
  222. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:Martin-Bell's syndrome
    n1=en:harrod doman keele syndrome | n2=en:Martin-Bell's syndrome | rel=r_associated | relid=0 | w=20
  223. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:mental retardation spasticity ectrodactyly
    n1=en:harrod doman keele syndrome | n2=en:mental retardation spasticity ectrodactyly | rel=r_associated | relid=0 | w=20
  224. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:nablus mask-like facial syndrome
    n1=en:harrod doman keele syndrome | n2=en:nablus mask-like facial syndrome | rel=r_associated | relid=0 | w=20
  225. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:nystagmus
    n1=en:harrod doman keele syndrome | n2=en:nystagmus | rel=r_associated | relid=0 | w=20
  226. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:physical defect
    n1=en:harrod doman keele syndrome | n2=en:physical defect | rel=r_associated | relid=0 | w=20
  227. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:piussan lenaerts mathieu syndrome
    n1=en:harrod doman keele syndrome | n2=en:piussan lenaerts mathieu syndrome | rel=r_associated | relid=0 | w=20
  228. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:ppp2r5d-related intellectual disability
    n1=en:harrod doman keele syndrome | n2=en:ppp2r5d-related intellectual disability | rel=r_associated | relid=0 | w=20
  229. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:Prader-Willi syndrome
    n1=en:harrod doman keele syndrome | n2=en:Prader-Willi syndrome | rel=r_associated | relid=0 | w=20
  230. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:rheumatic chorea
    n1=en:harrod doman keele syndrome | n2=en:rheumatic chorea | rel=r_associated | relid=0 | w=20
  231. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:scholte syndrome
    n1=en:harrod doman keele syndrome | n2=en:scholte syndrome | rel=r_associated | relid=0 | w=20
  232. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:short stature syndrome, brussels type
    n1=en:harrod doman keele syndrome | n2=en:short stature syndrome, brussels type | rel=r_associated | relid=0 | w=20
  233. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:spondyloepiphyseal dysplasia tarda kohn type
    n1=en:harrod doman keele syndrome | n2=en:spondyloepiphyseal dysplasia tarda kohn type | rel=r_associated | relid=0 | w=20
  234. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:Sydenham's chorea
    n1=en:harrod doman keele syndrome | n2=en:Sydenham's chorea | rel=r_associated | relid=0 | w=20
  235. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:teratosis
    n1=en:harrod doman keele syndrome | n2=en:teratosis | rel=r_associated | relid=0 | w=20
  236. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:thiamin-responsive maple syrup urine disease
    n1=en:harrod doman keele syndrome | n2=en:thiamin-responsive maple syrup urine disease | rel=r_associated | relid=0 | w=20
  237. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:trisomy
    n1=en:harrod doman keele syndrome | n2=en:trisomy | rel=r_associated | relid=0 | w=20
  238. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:trisomy xq28 syndrome
    n1=en:harrod doman keele syndrome | n2=en:trisomy xq28 syndrome | rel=r_associated | relid=0 | w=20
  239. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability armfield type
    n1=en:harrod doman keele syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
  240. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability miles carpenter type
    n1=en:harrod doman keele syndrome | n2=en:x-linked intellectual disability miles carpenter type | rel=r_associated | relid=0 | w=20
  241. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability pai type
    n1=en:harrod doman keele syndrome | n2=en:x-linked intellectual disability pai type | rel=r_associated | relid=0 | w=20
  242. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability seemanova type
    n1=en:harrod doman keele syndrome | n2=en:x-linked intellectual disability seemanova type | rel=r_associated | relid=0 | w=20
  243. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability stevenson type
    n1=en:harrod doman keele syndrome | n2=en:x-linked intellectual disability stevenson type | rel=r_associated | relid=0 | w=20
  244. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability stoll type
    n1=en:harrod doman keele syndrome | n2=en:x-linked intellectual disability stoll type | rel=r_associated | relid=0 | w=20
  245. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability van esch type
    n1=en:harrod doman keele syndrome | n2=en:x-linked intellectual disability van esch type | rel=r_associated | relid=0 | w=20
  246. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability with acromegaly and hyperactivity syndrome
    n1=en:harrod doman keele syndrome | n2=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | rel=r_associated | relid=0 | w=20
  247. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome
    n1=en:harrod doman keele syndrome | n2=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | rel=r_associated | relid=0 | w=20
  248. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome
    n1=en:harrod doman keele syndrome | n2=en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome | rel=r_associated | relid=0 | w=20
  249. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> exencéphalie
    n1=en:harrod doman keele syndrome | n2=exencéphalie | rel=r_associated | relid=0 | w=20
  250. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> goniodysgénésie-retard mental-petite taille (syndrome)
    n1=en:harrod doman keele syndrome | n2=goniodysgénésie-retard mental-petite taille (syndrome) | rel=r_associated | relid=0 | w=20
  251. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> histidinémie
    n1=en:harrod doman keele syndrome | n2=histidinémie | rel=r_associated | relid=0 | w=20
  252. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> kyste hydatique
    n1=en:harrod doman keele syndrome | n2=kyste hydatique | rel=r_associated | relid=0 | w=20
  253. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> leucinose
    n1=en:harrod doman keele syndrome | n2=leucinose | rel=r_associated | relid=0 | w=20
  254. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> lipofuscinose neuronale céroïde
    n1=en:harrod doman keele syndrome | n2=lipofuscinose neuronale céroïde | rel=r_associated | relid=0 | w=20
  255. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> lipofuscinose neuronale céroïde infantile finlandaise
    n1=en:harrod doman keele syndrome | n2=lipofuscinose neuronale céroïde infantile finlandaise | rel=r_associated | relid=0 | w=20
  256. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> maladie congénitale
    n1=en:harrod doman keele syndrome | n2=maladie congénitale | rel=r_associated | relid=0 | w=20
  257. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> maladie de Huntington
    n1=en:harrod doman keele syndrome | n2=maladie de Huntington | rel=r_associated | relid=0 | w=20
  258. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> Maladie de Huntington
    n1=en:harrod doman keele syndrome | n2=Maladie de Huntington | rel=r_associated | relid=0 | w=20
  259. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> maladie des urines à l'odeur de sirop d'érable
    n1=en:harrod doman keele syndrome | n2=maladie des urines à l'odeur de sirop d'érable | rel=r_associated | relid=0 | w=20
  260. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> maladie des urines avec odeur de sirop erable
    n1=en:harrod doman keele syndrome | n2=maladie des urines avec odeur de sirop erable | rel=r_associated | relid=0 | w=20
  261. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> maladie du sirop d'érable
    n1=en:harrod doman keele syndrome | n2=maladie du sirop d'érable | rel=r_associated | relid=0 | w=20
  262. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> malformation
    n1=en:harrod doman keele syndrome | n2=malformation | rel=r_associated | relid=0 | w=20
  263. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> malformation congénitale
    n1=en:harrod doman keele syndrome | n2=malformation congénitale | rel=r_associated | relid=0 | w=20
  264. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> nystagmus congénital isolé
    n1=en:harrod doman keele syndrome | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
  265. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> otocéphale
    n1=en:harrod doman keele syndrome | n2=otocéphale | rel=r_associated | relid=0 | w=20
  266. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> otocéphalie
    n1=en:harrod doman keele syndrome | n2=otocéphalie | rel=r_associated | relid=0 | w=20
  267. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> pathologie congénitale
    n1=en:harrod doman keele syndrome | n2=pathologie congénitale | rel=r_associated | relid=0 | w=20
  268. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> sclérose tubéreuse du cerveau
    n1=en:harrod doman keele syndrome | n2=sclérose tubéreuse du cerveau | rel=r_associated | relid=0 | w=20
  269. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> sirop d'érable (urine à odeur de)
    n1=en:harrod doman keele syndrome | n2=sirop d'érable (urine à odeur de) | rel=r_associated | relid=0 | w=20
  270. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> Syndrome d'Angelman
    n1=en:harrod doman keele syndrome | n2=Syndrome d'Angelman | rel=r_associated | relid=0 | w=20
  271. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'angelman
    n1=en:harrod doman keele syndrome | n2=syndrome d'angelman | rel=r_associated | relid=0 | w=20
  272. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'Angelman
    n1=en:harrod doman keele syndrome | n2=syndrome d'Angelman | rel=r_associated | relid=0 | w=20
  273. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> syndrome de de Barsy
    n1=en:harrod doman keele syndrome | n2=syndrome de de Barsy | rel=r_associated | relid=0 | w=20
  274. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> syndrome de De Barsy
    n1=en:harrod doman keele syndrome | n2=syndrome de De Barsy | rel=r_associated | relid=0 | w=20
  275. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> syndrome de de barsy
    n1=en:harrod doman keele syndrome | n2=syndrome de de barsy | rel=r_associated | relid=0 | w=20
  276. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> syndrome de fragilité du chromosome X
    n1=en:harrod doman keele syndrome | n2=syndrome de fragilité du chromosome X | rel=r_associated | relid=0 | w=20
  277. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Laurence-Moon
    n1=en:harrod doman keele syndrome | n2=syndrome de Laurence-Moon | rel=r_associated | relid=0 | w=20
  278. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Martin-Bell
    n1=en:harrod doman keele syndrome | n2=syndrome de Martin-Bell | rel=r_associated | relid=0 | w=20
  279. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Rett
    n1=en:harrod doman keele syndrome | n2=syndrome de Rett | rel=r_associated | relid=0 | w=20
  280. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> syndrome de rett
    n1=en:harrod doman keele syndrome | n2=syndrome de rett | rel=r_associated | relid=0 | w=20
  281. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> Syndrome de Rett
    n1=en:harrod doman keele syndrome | n2=Syndrome de Rett | rel=r_associated | relid=0 | w=20
  282. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> syndrome progéroïde de de barsy
    n1=en:harrod doman keele syndrome | n2=syndrome progéroïde de de barsy | rel=r_associated | relid=0 | w=20
  283. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> syndrome progéroïde de De Barsy
    n1=en:harrod doman keele syndrome | n2=syndrome progéroïde de De Barsy | rel=r_associated | relid=0 | w=20
  284. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> tare congénitale
    n1=en:harrod doman keele syndrome | n2=tare congénitale | rel=r_associated | relid=0 | w=20
  285. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> TPN ou NADP
    n1=en:harrod doman keele syndrome | n2=TPN ou NADP | rel=r_associated | relid=0 | w=20
  286. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> trisomie
    n1=en:harrod doman keele syndrome | n2=trisomie | rel=r_associated | relid=0 | w=20
  287. en:harrod doman keele syndrome -- r_associated #0: 20 / 0.465 -> vice de conformation
    n1=en:harrod doman keele syndrome | n2=vice de conformation | rel=r_associated | relid=0 | w=20
  288. en:harrod doman keele syndrome -- r_associated #0: 1 / 0.023 -> maladie de marfan
    n1=en:harrod doman keele syndrome | n2=maladie de marfan | rel=r_associated | relid=0 | w=1
≈ 434 relations entrantes

  1. anomalie congénitale --- r_associated #0: 334 --> en:harrod doman keele syndrome
    n1=anomalie congénitale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=334
  2. en:congenital abnormality --- r_associated #0: 332 --> en:harrod doman keele syndrome
    n1=en:congenital abnormality | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=332
  3. malformation congénitale --- r_associated #0: 311 --> en:harrod doman keele syndrome
    n1=malformation congénitale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=311
  4. en:congenital defect --- r_associated #0: 310 --> en:harrod doman keele syndrome
    n1=en:congenital defect | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=310
  5. en:congenital anomaly --- r_associated #0: 309 --> en:harrod doman keele syndrome
    n1=en:congenital anomaly | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=309
  6. déformation congénitale --- r_associated #0: 296 --> en:harrod doman keele syndrome
    n1=déformation congénitale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=296
  7. déficience congénitale --- r_associated #0: 295 --> en:harrod doman keele syndrome
    n1=déficience congénitale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=295
  8. chorée de saint jean --- r_associated #0: 220 --> en:harrod doman keele syndrome
    n1=chorée de saint jean | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=220
  9. chorées --- r_associated #0: 220 --> en:harrod doman keele syndrome
    n1=chorées | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=220
  10. danse de saint Guy --- r_associated #0: 220 --> en:harrod doman keele syndrome
    n1=danse de saint Guy | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=220
  11. en:rheumatic chorea --- r_associated #0: 213 --> en:harrod doman keele syndrome
    n1=en:rheumatic chorea | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=213
  12. chorée héréditaire --- r_associated #0: 210 --> en:harrod doman keele syndrome
    n1=chorée héréditaire | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=210
  13. chorée rhumatismale --- r_associated #0: 210 --> en:harrod doman keele syndrome
    n1=chorée rhumatismale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=210
  14. chorée rhumatismale sans atteinte cardiaque --- r_associated #0: 210 --> en:harrod doman keele syndrome
    n1=chorée rhumatismale sans atteinte cardiaque | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=210
  15. chorée de Huntington --- r_associated #0: 208 --> en:harrod doman keele syndrome
    n1=chorée de Huntington | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=208
  16. en:huntington's disease --- r_associated #0: 207 --> en:harrod doman keele syndrome
    n1=en:huntington's disease | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=207
  17. Chorée --- r_associated #0: 206 --> en:harrod doman keele syndrome
    n1=Chorée | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=206
  18. dysplasie fronto-nasale acromélique --- r_associated #0: 206 --> en:harrod doman keele syndrome
    n1=dysplasie fronto-nasale acromélique | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=206
  19. dysostose fronto-nasale acromélique --- r_associated #0: 205 --> en:harrod doman keele syndrome
    n1=dysostose fronto-nasale acromélique | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=205
  20. en:acromelic frontonasal dysostosis --- r_associated #0: 205 --> en:harrod doman keele syndrome
    n1=en:acromelic frontonasal dysostosis | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=205
  21. maladie de Huntington --- r_associated #0: 205 --> en:harrod doman keele syndrome
    n1=maladie de Huntington | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=205
  22. difformité congénitale --- r_associated #0: 200 --> en:harrod doman keele syndrome
    n1=difformité congénitale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=200
  23. chorée de Sydenham --- r_associated #0: 190 --> en:harrod doman keele syndrome
    n1=chorée de Sydenham | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=190
  24. maladie congénitale --- r_associated #0: 190 --> en:harrod doman keele syndrome
    n1=maladie congénitale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=190
  25. pathologie congénitale --- r_associated #0: 185 --> en:harrod doman keele syndrome
    n1=pathologie congénitale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=185
  26. en:angelman syndrome --- r_associated #0: 134 --> en:harrod doman keele syndrome
    n1=en:angelman syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=134
  27. en:congenital malformation --- r_associated #0: 130 --> en:harrod doman keele syndrome
    n1=en:congenital malformation | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=130
  28. syndrome d'Angelman --- r_associated #0: 130 --> en:harrod doman keele syndrome
    n1=syndrome d'Angelman | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=130
  29. en:birth defect --- r_associated #0: 120 --> en:harrod doman keele syndrome
    n1=en:birth defect | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=120
  30. syndrome de Rett --- r_associated #0: 100 --> en:harrod doman keele syndrome
    n1=syndrome de Rett | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=100
  31. en:rett syndrome --- r_associated #0: 98 --> en:harrod doman keele syndrome
    n1=en:rett syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=98
  32. exencéphalie --- r_associated #0: 98 --> en:harrod doman keele syndrome
    n1=exencéphalie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=98
  33. en:exencephaly --- r_associated #0: 95 --> en:harrod doman keele syndrome
    n1=en:exencephaly | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=95
  34. en:Angelman syndrome --- r_associated #0: 90 --> en:harrod doman keele syndrome
    n1=en:Angelman syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=90
  35. en:Huntington's disease --- r_associated #0: 90 --> en:harrod doman keele syndrome
    n1=en:Huntington's disease | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=90
  36. tare congénitale --- r_associated #0: 85 --> en:harrod doman keele syndrome
    n1=tare congénitale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=85
  37. sclérose tubéreuse du cerveau --- r_associated #0: 80 --> en:harrod doman keele syndrome
    n1=sclérose tubéreuse du cerveau | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=80
  38. en:tuberous sclerosis --- r_associated #0: 79 --> en:harrod doman keele syndrome
    n1=en:tuberous sclerosis | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=79
  39. en:fragile x syndrome --- r_associated #0: 76 --> en:harrod doman keele syndrome
    n1=en:fragile x syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=76
  40. en:fragile X syndrome --- r_associated #0: 75 --> en:harrod doman keele syndrome
    n1=en:fragile X syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=75
  41. congenital --- r_associated #0: 72 --> en:harrod doman keele syndrome
    n1=congenital | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=72
  42. Syndrome d'Angelman --- r_associated #0: 70 --> en:harrod doman keele syndrome
    n1=Syndrome d'Angelman | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=70
  43. syndrome de fragilité du chromosome X --- r_associated #0: 70 --> en:harrod doman keele syndrome
    n1=syndrome de fragilité du chromosome X | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=70
  44. en:cyclopia --- r_associated #0: 68 --> en:harrod doman keele syndrome
    n1=en:cyclopia | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=68
  45. cyclopie --- r_associated #0: 67 --> en:harrod doman keele syndrome
    n1=cyclopie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=67
  46. Syndrome de Rett --- r_associated #0: 65 --> en:harrod doman keele syndrome
    n1=Syndrome de Rett | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=65
  47. cyclopia --- r_associated #0: 65 --> en:harrod doman keele syndrome
    n1=cyclopia | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=65
  48. en:congenital --- r_associated #0: 65 --> en:harrod doman keele syndrome
    n1=en:congenital | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=65
  49. kyste hydatique --- r_associated #0: 65 --> en:harrod doman keele syndrome
    n1=kyste hydatique | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=65
  50. en:Klinefelter syndrome --- r_associated #0: 62 --> en:harrod doman keele syndrome
    n1=en:Klinefelter syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=62
  51. en:de barsy syndrome --- r_associated #0: 62 --> en:harrod doman keele syndrome
    n1=en:de barsy syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=62
  52. syndrome de de barsy --- r_associated #0: 62 --> en:harrod doman keele syndrome
    n1=syndrome de de barsy | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=62
  53. en:hydatid cyst --- r_associated #0: 61 --> en:harrod doman keele syndrome
    n1=en:hydatid cyst | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=61
  54. en:klinefelter syndrome --- r_associated #0: 61 --> en:harrod doman keele syndrome
    n1=en:klinefelter syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=61
  55. syndrome d'angelman --- r_associated #0: 61 --> en:harrod doman keele syndrome
    n1=syndrome d'angelman | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=61
  56. syndrome de De Barsy --- r_associated #0: 61 --> en:harrod doman keele syndrome
    n1=syndrome de De Barsy | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=61
  57. syndrome progéroïde de De Barsy --- r_associated #0: 61 --> en:harrod doman keele syndrome
    n1=syndrome progéroïde de De Barsy | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=61
  58. syndrome de de Barsy --- r_associated #0: 60 --> en:harrod doman keele syndrome
    n1=syndrome de de Barsy | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=60
  59. syndrome de rett --- r_associated #0: 58 --> en:harrod doman keele syndrome
    n1=syndrome de rett | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=58
  60. vice de conformation --- r_associated #0: 57 --> en:harrod doman keele syndrome
    n1=vice de conformation | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=57
  61. congénitale --- r_associated #0: 55 --> en:harrod doman keele syndrome
    n1=congénitale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=55
  62. en:down syndrome --- r_associated #0: 53 --> en:harrod doman keele syndrome
    n1=en:down syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=53
  63. en:teratosis --- r_associated #0: 53 --> en:harrod doman keele syndrome
    n1=en:teratosis | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=53
  64. en:major physical defect --- r_associated #0: 51 --> en:harrod doman keele syndrome
    n1=en:major physical defect | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=51
  65. en:Down syndrome --- r_associated #0: 50 --> en:harrod doman keele syndrome
    n1=en:Down syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=50
  66. chorée de huntington --- r_associated #0: 47 --> en:harrod doman keele syndrome
    n1=chorée de huntington | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=47
  67. en:prader-willi syndrome --- r_associated #0: 47 --> en:harrod doman keele syndrome
    n1=en:prader-willi syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=47
  68. chorée de sydenham --- r_associated #0: 46 --> en:harrod doman keele syndrome
    n1=chorée de sydenham | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=46
  69. en:Prader-Willi syndrome --- r_associated #0: 45 --> en:harrod doman keele syndrome
    n1=en:Prader-Willi syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=45
  70. otocéphale --- r_associated #0: 44 --> en:harrod doman keele syndrome
    n1=otocéphale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=44
  71. anomalie du développement --- r_associated #0: 43 --> en:harrod doman keele syndrome
    n1=anomalie du développement | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=43
  72. en:ambiguous genitalia --- r_associated #0: 43 --> en:harrod doman keele syndrome
    n1=en:ambiguous genitalia | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=43
  73. en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 43 --> en:harrod doman keele syndrome
    n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=43
  74. goniodysgénésie-retard mental-petite taille (syndrome) --- r_associated #0: 43 --> en:harrod doman keele syndrome
    n1=goniodysgénésie-retard mental-petite taille (syndrome) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=43
  75. sirop d'érable (urine à odeur de) --- r_associated #0: 43 --> en:harrod doman keele syndrome
    n1=sirop d'érable (urine à odeur de) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=43
  76. en:char syndrome --- r_associated #0: 42 --> en:harrod doman keele syndrome
    n1=en:char syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=42
  77. en:physical defect --- r_associated #0: 42 --> en:harrod doman keele syndrome
    n1=en:physical defect | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=42
  78. en:karandikar maria kamble syndrome --- r_associated #0: 41 --> en:harrod doman keele syndrome
    n1=en:karandikar maria kamble syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=41
  79. en:x-linked intellectual disability seemanova type --- r_associated #0: 41 --> en:harrod doman keele syndrome
    n1=en:x-linked intellectual disability seemanova type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=41
  80. déficit en céto-acide décarboxylase --- r_associated #0: 40 --> en:harrod doman keele syndrome
    n1=déficit en céto-acide décarboxylase | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=40
  81. en:classical maple syrup urine disease --- r_associated #0: 40 --> en:harrod doman keele syndrome
    n1=en:classical maple syrup urine disease | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=40
  82. en:maple syrup urine disease --- r_associated #0: 40 --> en:harrod doman keele syndrome
    n1=en:maple syrup urine disease | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=40
  83. en:renpenning syndrome 1 --- r_associated #0: 40 --> en:harrod doman keele syndrome
    n1=en:renpenning syndrome 1 | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=40
  84. en:thiamin-responsive maple syrup urine disease --- r_associated #0: 40 --> en:harrod doman keele syndrome
    n1=en:thiamin-responsive maple syrup urine disease | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=40
  85. leucinose --- r_associated #0: 40 --> en:harrod doman keele syndrome
    n1=leucinose | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=40
  86. maladie des urines avec odeur de sirop erable --- r_associated #0: 40 --> en:harrod doman keele syndrome
    n1=maladie des urines avec odeur de sirop erable | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=40
  87. maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 40 --> en:harrod doman keele syndrome
    n1=maladie des urines à l'odeur de sirop d'érable | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=40
  88. maladie du sirop d'érable --- r_associated #0: 40 --> en:harrod doman keele syndrome
    n1=maladie du sirop d'érable | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=40
  89. en:exenkephaly --- r_associated #0: 39 --> en:harrod doman keele syndrome
    n1=en:exenkephaly | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=39
  90. en:goniodysgenesis-mental retardation-short stature syndrome --- r_associated #0: 39 --> en:harrod doman keele syndrome
    n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=39
  91. en:grob's syndrome --- r_associated #0: 39 --> en:harrod doman keele syndrome
    n1=en:grob's syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=39
  92. en:hydatic cyst --- r_associated #0: 39 --> en:harrod doman keele syndrome
    n1=en:hydatic cyst | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=39
  93. en:Gaucher disease --- r_associated #0: 38 --> en:harrod doman keele syndrome
    n1=en:Gaucher disease | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=38
  94. en:fryns macrocephaly --- r_associated #0: 38 --> en:harrod doman keele syndrome
    n1=en:fryns macrocephaly | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=38
  95. en:indeterminate sex and pseudohermaphroditism --- r_associated #0: 38 --> en:harrod doman keele syndrome
    n1=en:indeterminate sex and pseudohermaphroditism | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=38
  96. en:marfanoid mental retardation syndrome --- r_associated #0: 38 --> en:harrod doman keele syndrome
    n1=en:marfanoid mental retardation syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=38
  97. en:savant syndrome --- r_associated #0: 38 --> en:harrod doman keele syndrome
    n1=en:savant syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=38
  98. Maladie de Huntington --- r_associated #0: 37 --> en:harrod doman keele syndrome
    n1=Maladie de Huntington | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=37
  99. congénital --- r_associated #0: 35 --> en:harrod doman keele syndrome
    n1=congénital | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=35
  100. en:17q11.2 microduplication syndrome --- r_associated #0: 35 --> en:harrod doman keele syndrome
    n1=en:17q11.2 microduplication syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=35
  101. en:arachnodactyly and intellectual disability with facial dysmorphism syndrome --- r_associated #0: 35 --> en:harrod doman keele syndrome
    n1=en:arachnodactyly and intellectual disability with facial dysmorphism syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=35
  102. en:arhinia, choanal atresia, and microphthalmia --- r_associated #0: 35 --> en:harrod doman keele syndrome
    n1=en:arhinia, choanal atresia, and microphthalmia | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=35
  103. en:cooper jabs syndrome --- r_associated #0: 35 --> en:harrod doman keele syndrome
    n1=en:cooper jabs syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=35
  104. en:fountain syndrome --- r_associated #0: 35 --> en:harrod doman keele syndrome
    n1=en:fountain syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=35
  105. en:marshall syndrome --- r_associated #0: 35 --> en:harrod doman keele syndrome
    n1=en:marshall syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=35
  106. en:microcephaly deafness syndrome --- r_associated #0: 35 --> en:harrod doman keele syndrome
    n1=en:microcephaly deafness syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=35
  107. en:morm syndrome --- r_associated #0: 35 --> en:harrod doman keele syndrome
    n1=en:morm syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=35
  108. en:multiple malformation syndrome with facial-limb defects as major feature --- r_associated #0: 35 --> en:harrod doman keele syndrome
    n1=en:multiple malformation syndrome with facial-limb defects as major feature | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=35
  109. en:nablus mask-like facial syndrome --- r_associated #0: 35 --> en:harrod doman keele syndrome
    n1=en:nablus mask-like facial syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=35
  110. en:other mental retardation --- r_associated #0: 35 --> en:harrod doman keele syndrome
    n1=en:other mental retardation | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=35
  111. en:x-linked intellectual disability armfield type --- r_associated #0: 35 --> en:harrod doman keele syndrome
    n1=en:x-linked intellectual disability armfield type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=35
  112. en:aniridia and intellectual disability syndrome --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:aniridia and intellectual disability syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  113. en:craniofacial abnormalities --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:craniofacial abnormalities | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  114. en:fraxe intellectual disability syndrome --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:fraxe intellectual disability syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  115. en:gaucher disease --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:gaucher disease | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  116. en:haspeslagh fryns muelenaere syndrome --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:haspeslagh fryns muelenaere syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  117. en:hypospadias-mental retardation syndrome --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:hypospadias-mental retardation syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  118. en:lissencephaly syndrome, norman-roberts type --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:lissencephaly syndrome, norman-roberts type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  119. en:mcdonough syndrome --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:mcdonough syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  120. en:microphthalmia, syndromic 4 (disorder) --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:microphthalmia, syndromic 4 (disorder) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  121. en:neuronal ceroid lipofuscinosis --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:neuronal ceroid lipofuscinosis | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  122. en:opitz trigonocephaly syndrome --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:opitz trigonocephaly syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  123. en:ppp2r5d-related intellectual disability --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:ppp2r5d-related intellectual disability | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  124. en:pseudotrisomy 13 syndrome --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  125. en:severe mental retardation (i.q. 20-34) --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:severe mental retardation (i.q. 20-34) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  126. en:short stature syndrome, brussels type --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:short stature syndrome, brussels type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  127. en:spondyloepiphyseal dysplasia tarda kohn type --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:spondyloepiphyseal dysplasia tarda kohn type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  128. en:treacher collins syndrome --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:treacher collins syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  129. en:x-linked intellectual disability pai type --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:x-linked intellectual disability pai type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  130. en:x-linked intellectual disability stoll type --- r_associated #0: 34 --> en:harrod doman keele syndrome
    n1=en:x-linked intellectual disability stoll type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  131. en:maple-tree syrup disease --- r_associated #0: 33 --> en:harrod doman keele syndrome
    n1=en:maple-tree syrup disease | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=33
  132. lipofuscinose neuronale céroïde infantile finlandaise --- r_associated #0: 33 --> en:harrod doman keele syndrome
    n1=lipofuscinose neuronale céroïde infantile finlandaise | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=33
  133. en:congenital anomaly of male genital system --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:congenital anomaly of male genital system | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  134. en:congenital contractural arachnodactyly --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:congenital contractural arachnodactyly | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  135. en:cranio-orbito-ocular dysraphia syndrome --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:cranio-orbito-ocular dysraphia syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  136. en:fronto-naso-ethmoidal dysostosis --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:fronto-naso-ethmoidal dysostosis | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  137. en:halal syndrome --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:halal syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  138. en:hall riggs syndrome --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:hall riggs syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  139. en:kabuki syndrome --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:kabuki syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  140. en:kosztolanyi syndrome --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:kosztolanyi syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  141. en:leucinosis --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:leucinosis | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  142. en:melnick-fraser syndrome --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:melnick-fraser syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  143. en:mental retardation, x-linked, snyder-robinson type --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:mental retardation, x-linked, snyder-robinson type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  144. en:persistent urogenital sinus --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:persistent urogenital sinus | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  145. en:rozin hertz goodman syndrome --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:rozin hertz goodman syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  146. en:shprintzen omphalocele syndrome --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:shprintzen omphalocele syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  147. en:undescended and ectopic testicle --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:undescended and ectopic testicle | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  148. en:wildervanck's syndrome --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:wildervanck's syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  149. en:x-linked intellectual disability miles carpenter type --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:x-linked intellectual disability miles carpenter type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  150. en:x-linked intellectual disability van esch type --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:x-linked intellectual disability van esch type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  151. en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome --- r_associated #0: 32 --> en:harrod doman keele syndrome
    n1=en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=32
  152. en:borderline mental retardation (i.q. 70-85) --- r_associated #0: 31 --> en:harrod doman keele syndrome
    n1=en:borderline mental retardation (i.q. 70-85) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=31
  153. en:brachioskeletogenital syndrome --- r_associated #0: 31 --> en:harrod doman keele syndrome
    n1=en:brachioskeletogenital syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=31
  154. en:frontonasal dysplasia sequence --- r_associated #0: 31 --> en:harrod doman keele syndrome
    n1=en:frontonasal dysplasia sequence | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=31
  155. en:growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate --- r_associated #0: 31 --> en:harrod doman keele syndrome
    n1=en:growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=31
  156. en:hypomandibular faciocranial dysostosis --- r_associated #0: 31 --> en:harrod doman keele syndrome
    n1=en:hypomandibular faciocranial dysostosis | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=31
  157. en:ichthyosis--cheek--eyebrow syndrome --- r_associated #0: 31 --> en:harrod doman keele syndrome
    n1=en:ichthyosis--cheek--eyebrow syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=31
  158. en:lujan fryns syndrome --- r_associated #0: 31 --> en:harrod doman keele syndrome
    n1=en:lujan fryns syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=31
  159. en:mowat-wilson syndrome --- r_associated #0: 31 --> en:harrod doman keele syndrome
    n1=en:mowat-wilson syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=31
  160. en:nutritional mental retardation --- r_associated #0: 31 --> en:harrod doman keele syndrome
    n1=en:nutritional mental retardation | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=31
  161. histidinémie --- r_associated #0: 31 --> en:harrod doman keele syndrome
    n1=histidinémie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=31
  162. lipofuscinose neuronale céroïde --- r_associated #0: 31 --> en:harrod doman keele syndrome
    n1=lipofuscinose neuronale céroïde | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=31
  163. nystagmus congénital isolé --- r_associated #0: 31 --> en:harrod doman keele syndrome
    n1=nystagmus congénital isolé | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=31
  164. syndrome de Martin-Bell --- r_associated #0: 31 --> en:harrod doman keele syndrome
    n1=syndrome de Martin-Bell | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=31
  165. Chopart (désarticulation de) --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=Chopart (désarticulation de) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  166. en:Martin-Bell's syndrome --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:Martin-Bell's syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  167. en:bardet-biedl syndrome --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:bardet-biedl syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  168. en:blepharophimosis syndrome ohdo type --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:blepharophimosis syndrome ohdo type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  169. en:branched-chain ketoaciduria --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:branched-chain ketoaciduria | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  170. en:cask related intellectual disability --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:cask related intellectual disability | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  171. en:developmental fault --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:developmental fault | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  172. en:dysmorphism, pectus carinatum, joint laxity syndrome --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:dysmorphism, pectus carinatum, joint laxity syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  173. en:female restricted epilepsy with intellectual disability syndrome --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:female restricted epilepsy with intellectual disability syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  174. en:goldenhar syndrome --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:goldenhar syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  175. en:localized congenital skull defect --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:localized congenital skull defect | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  176. en:nystagmus --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:nystagmus | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  177. en:partington x-linked mental retardation syndrome --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:partington x-linked mental retardation syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  178. en:scholte syndrome --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:scholte syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  179. en:trisomy xq28 syndrome --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:trisomy xq28 syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  180. en:undescended and retractile testicle --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:undescended and retractile testicle | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  181. en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  182. en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  183. en:waardenburg syndrome --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:waardenburg syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  184. en:wellesley carman french syndrome --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=en:wellesley carman french syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  185. nystagmus --- r_associated #0: 30 --> en:harrod doman keele syndrome
    n1=nystagmus | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=30
  186. en:1p21.3 microdeletion syndrome --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=en:1p21.3 microdeletion syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  187. en:blepharophimosis, ptosis, and epicanthus inversus (disorder) --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=en:blepharophimosis, ptosis, and epicanthus inversus (disorder) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  188. en:cayler cardiofacial syndrome --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=en:cayler cardiofacial syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  189. en:chromosome 17, trisomy 17p --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=en:chromosome 17, trisomy 17p | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  190. en:coffin-siris syndrome --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=en:coffin-siris syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  191. en:deafness-craniofacial syndrome --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=en:deafness-craniofacial syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  192. en:fronto-facio-nasal dysplasia --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=en:fronto-facio-nasal dysplasia | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  193. en:hypertrichosis and acromegaloid facial appearance syndrome --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=en:hypertrichosis and acromegaloid facial appearance syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  194. en:kohlschutter tonz syndrome --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=en:kohlschutter tonz syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  195. en:mental retardation spasticity ectrodactyly --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=en:mental retardation spasticity ectrodactyly | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  196. en:oculocerebrorenal syndrome --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=en:oculocerebrorenal syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  197. en:other congenital malformations of female genitalia --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=en:other congenital malformations of female genitalia | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  198. en:unspecified mental retardation; without mention of impairment of behaviour --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=en:unspecified mental retardation; without mention of impairment of behaviour | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  199. en:van der woude syndrome --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=en:van der woude syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  200. malformation --- r_associated #0: 29 --> en:harrod doman keele syndrome
    n1=malformation | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=29
  201. Maladie congénitale --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=Maladie congénitale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  202. en:Sydenham's chorea --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=en:Sydenham's chorea | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  203. en:classical phenylketonuria --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=en:classical phenylketonuria | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  204. en:cleft lip sequence --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=en:cleft lip sequence | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  205. en:congenital anomaly of jaw --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=en:congenital anomaly of jaw | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  206. en:congenital anomaly of ovary --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=en:congenital anomaly of ovary | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  207. en:crane-heise syndrome --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=en:crane-heise syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  208. en:fried syndrome --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=en:fried syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  209. en:gurrieri sammito bellussi syndrome --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=en:gurrieri sammito bellussi syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  210. en:lesch-nyhan syndrome --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=en:lesch-nyhan syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  211. en:prader-willi habitus, osteopenia, and camptodactyly --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=en:prader-willi habitus, osteopenia, and camptodactyly | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  212. en:profound intellectual disabilities --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=en:profound intellectual disabilities | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  213. en:wolf-hirschhorn syndrome --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=en:wolf-hirschhorn syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  214. en:x-linked intellectual disability stevenson type --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=en:x-linked intellectual disability stevenson type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  215. en:x-linked intellectual disability with acromegaly and hyperactivity syndrome --- r_associated #0: 28 --> en:harrod doman keele syndrome
    n1=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=28
  216. TPN ou NADP --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=TPN ou NADP | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  217. arachnodactylie et contractures congénitales --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=arachnodactylie et contractures congénitales | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  218. en:12q14 microdeletion syndrome --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:12q14 microdeletion syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  219. en:abnormally long growth --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:abnormally long growth | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  220. en:chromosome 17q21.31 deletion syndrome --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:chromosome 17q21.31 deletion syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  221. en:congenital anomaly of female genital system --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:congenital anomaly of female genital system | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  222. en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  223. en:congenital malformations of ovaries, fallopian tubes and broad ligaments --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:congenital malformations of ovaries, fallopian tubes and broad ligaments | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  224. en:craniofrontonasal dysplasia --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:craniofrontonasal dysplasia | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  225. en:de sanctis-cacchione syndrome --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:de sanctis-cacchione syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  226. en:echinococcus cyst --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:echinococcus cyst | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  227. en:fronto-frontal dysostosis --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:fronto-frontal dysostosis | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  228. en:histidinemia --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:histidinemia | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  229. en:hyperphosphatasia with mental retardation --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:hyperphosphatasia with mental retardation | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  230. en:masa syndrome (disorder) --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:masa syndrome (disorder) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  231. en:maxillonasal dysplasia, binder type --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:maxillonasal dysplasia, binder type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  232. en:mehes syndrome --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:mehes syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  233. en:mesonephric cyst --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:mesonephric cyst | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  234. en:pierre robin syndrome --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:pierre robin syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  235. en:piussan lenaerts mathieu syndrome --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:piussan lenaerts mathieu syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  236. en:spheno-frontal dysostosis --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:spheno-frontal dysostosis | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  237. en:thomas syndrome --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:thomas syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  238. en:trisomy --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:trisomy | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  239. en:uterus bilocularis --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=en:uterus bilocularis | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  240. syndrome progéroïde de de barsy --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=syndrome progéroïde de de barsy | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  241. triskélion --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=triskélion | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  242. trisomie --- r_associated #0: 27 --> en:harrod doman keele syndrome
    n1=trisomie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=27
  243. cétoacidurie à chaînes ramifiées --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=cétoacidurie à chaînes ramifiées | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  244. en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:ectodermal dysplasia with blindness syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  245. en:fara chlupackova syndrome --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:fara chlupackova syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  246. en:gonadal dysgenesis --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:gonadal dysgenesis | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  247. en:histidinaemia --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:histidinaemia | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  248. en:laurence-moon syndrome --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:laurence-moon syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  249. en:lissencephaly, x-linked, 2 --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:lissencephaly, x-linked, 2 | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  250. en:lubs x-linked mental retardation syndrome --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:lubs x-linked mental retardation syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  251. en:membranous cranial ossification, delayed --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:membranous cranial ossification, delayed | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  252. en:o/e - hands - arachnodactyly --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:o/e - hands - arachnodactyly | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  253. en:otocephaly --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:otocephaly | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  254. en:perniola krajewska carnevale syndrome --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:perniola krajewska carnevale syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  255. en:smith-magenis syndrome --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:smith-magenis syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  256. en:sonoda syndrome --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:sonoda syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  257. en:streak gonad --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:streak gonad | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  258. en:syndrome, branchio-oculo-facial --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:syndrome, branchio-oculo-facial | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  259. en:syndromic orbital border hypoplasia --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:syndromic orbital border hypoplasia | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  260. en:trisomy 10p --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:trisomy 10p | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  261. en:undescended testes --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:undescended testes | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  262. en:unspecified mental retardation; other impairments of behaviour --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:unspecified mental retardation; other impairments of behaviour | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  263. en:waisman syndrome --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:waisman syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  264. en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  265. otocéphalie --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=otocéphalie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  266. syndrome de Laurence-Moon --- r_associated #0: 26 --> en:harrod doman keele syndrome
    n1=syndrome de Laurence-Moon | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=26
  267. en:Laurence-Moon's syndrome --- r_associated #0: 25 --> en:harrod doman keele syndrome
    n1=en:Laurence-Moon's syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=25
  268. en:congenital anomaly of skull --- r_associated #0: 25 --> en:harrod doman keele syndrome
    n1=en:congenital anomaly of skull | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=25
  269. en:intellectual disability --- r_associated #0: 25 --> en:harrod doman keele syndrome
    n1=en:intellectual disability | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=25
  270. en:monopia --- r_associated #0: 25 --> en:harrod doman keele syndrome
    n1=en:monopia | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=25
  271. en:orotic aciduria --- r_associated #0: 25 --> en:harrod doman keele syndrome
    n1=en:orotic aciduria | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=25
  272. une anomalie congénitale --- r_associated #0: 25 --> en:harrod doman keele syndrome
    n1=une anomalie congénitale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=25
  273. contractures congénitales et arachnodactylie --- r_associated #0: 24 --> en:harrod doman keele syndrome
    n1=contractures congénitales et arachnodactylie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=24
  274. en:congenital malformation of uterus and cervix --- r_associated #0: 24 --> en:harrod doman keele syndrome
    n1=en:congenital malformation of uterus and cervix | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=24
  275. en:fryns syndrome --- r_associated #0: 24 --> en:harrod doman keele syndrome
    n1=en:fryns syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=24
  276. en:moderate mental retardation (i.q. 35-49) --- r_associated #0: 24 --> en:harrod doman keele syndrome
    n1=en:moderate mental retardation (i.q. 35-49) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=24
  277. en:other specified anomalies of genital organs --- r_associated #0: 24 --> en:harrod doman keele syndrome
    n1=en:other specified anomalies of genital organs | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=24
  278. en:unspecified anomaly of cervix, vagina, and external female genitalia --- r_associated #0: 24 --> en:harrod doman keele syndrome
    n1=en:unspecified anomaly of cervix, vagina, and external female genitalia | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=24
  279. en:Angelman's syndrome --- r_associated #0: 23 --> en:harrod doman keele syndrome
    n1=en:Angelman's syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=23
  280. en:developmental anomaly --- r_associated #0: 23 --> en:harrod doman keele syndrome
    n1=en:developmental anomaly | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=23
  281. en:hypospadias and epispadias and other penile anomalies --- r_associated #0: 23 --> en:harrod doman keele syndrome
    n1=en:hypospadias and epispadias and other penile anomalies | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=23
  282. en:mild mental retardation --- r_associated #0: 23 --> en:harrod doman keele syndrome
    n1=en:mild mental retardation | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=23
  283. en:multiple congenital anomalies --- r_associated #0: 23 --> en:harrod doman keele syndrome
    n1=en:multiple congenital anomalies | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=23
  284. sclérodermie tubéreuse de bourneville --- r_associated #0: 23 --> en:harrod doman keele syndrome
    n1=sclérodermie tubéreuse de bourneville | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=23
  285. en:borjeson-forssman-lehmann syndrome --- r_associated #0: 22 --> en:harrod doman keele syndrome
    n1=en:borjeson-forssman-lehmann syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=22
  286. en:congenital anomaly of face bones --- r_associated #0: 22 --> en:harrod doman keele syndrome
    n1=en:congenital anomaly of face bones | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=22
  287. en:cyst of embryonic remnant - male --- r_associated #0: 22 --> en:harrod doman keele syndrome
    n1=en:cyst of embryonic remnant - male | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=22
  288. en:cyst of wolffian duct --- r_associated #0: 22 --> en:harrod doman keele syndrome
    n1=en:cyst of wolffian duct | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=22
  289. en:duplication of external genitalia --- r_associated #0: 22 --> en:harrod doman keele syndrome
    n1=en:duplication of external genitalia | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=22
  290. en:fallopian tube and broad ligament anomalies --- r_associated #0: 22 --> en:harrod doman keele syndrome
    n1=en:fallopian tube and broad ligament anomalies | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=22
  291. en:kaufman-mckusick syndrome --- r_associated #0: 22 --> en:harrod doman keele syndrome
    n1=en:kaufman-mckusick syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=22
  292. en:myopathy, congenital nonprogressive with moebius and robin sequences --- r_associated #0: 22 --> en:harrod doman keele syndrome
    n1=en:myopathy, congenital nonprogressive with moebius and robin sequences | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=22
  293. en:other anomalies of uterus --- r_associated #0: 22 --> en:harrod doman keele syndrome
    n1=en:other anomalies of uterus | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=22
  294. en:de Barsy's syndrome --- r_associated #0: 21 --> en:harrod doman keele syndrome
    n1=en:de Barsy's syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=21
  295. en:encephalocele --- r_associated #0: 21 --> en:harrod doman keele syndrome
    n1=en:encephalocele | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=21
  296. en:homocystinuria --- r_associated #0: 21 --> en:harrod doman keele syndrome
    n1=en:homocystinuria | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=21
  297. en:hypospadias --- r_associated #0: 21 --> en:harrod doman keele syndrome
    n1=en:hypospadias | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=21
  298. syndrome de Prader-Willi --- r_associated #0: 21 --> en:harrod doman keele syndrome
    n1=syndrome de Prader-Willi | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=21
  299. Malformation --- r_associated #0: 20 --> en:harrod doman keele syndrome
    n1=Malformation | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=20
  300. Malformation congénitale --- r_associated #0: 20 --> en:harrod doman keele syndrome
    n1=Malformation congénitale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=20
  301. en:Smith-Magenis syndrome --- r_associated #0: 20 --> en:harrod doman keele syndrome
    n1=en:Smith-Magenis syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=20
  302. syndrome --- r_associated #0: 20 --> en:harrod doman keele syndrome
    n1=syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=20
  303. hypospadias --- r_associated #0: 17 --> en:harrod doman keele syndrome
    n1=hypospadias | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=17
  304. trisomie 21 --- r_associated #0: 16 --> en:harrod doman keele syndrome
    n1=trisomie 21 | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=16
  305. CONGÉNITALE --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=CONGÉNITALE | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  306. His (faisceau de) --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=His (faisceau de) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  307. cyclope (oeil) --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=cyclope (oeil) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  308. en:trismus --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=en:trismus | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  309. exécutives (fonctions) --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=exécutives (fonctions) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  310. malentendant (enfant) --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=malentendant (enfant) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  311. triple arthrodèse --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=triple arthrodèse | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  312. triple opération à la française --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=triple opération à la française | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  313. triploïdie --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=triploïdie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  314. triptans --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=triptans | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  315. triquétrum --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=triquétrum | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  316. triradialis sulcus de Turner --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=triradialis sulcus de Turner | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  317. tris --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=tris | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  318. trismus --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=trismus | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  319. trisomie du bras court du chromosome 3 --- r_associated #0: 15 --> en:harrod doman keele syndrome
    n1=trisomie du bras court du chromosome 3 | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=15
  320. mongolisme --- r_associated #0: 11 --> en:harrod doman keele syndrome
    n1=mongolisme | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=11
  321. Angelman (syndrome d') --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=Angelman (syndrome d') | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  322. CONGENITAL --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=CONGENITAL | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  323. Chorée de Huntington --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=Chorée de Huntington | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  324. Congenital --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=Congenital | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  325. Histidinémie --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=Histidinémie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  326. Laurence-Moon (syndrome de) --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=Laurence-Moon (syndrome de) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  327. Martin-Bell (syndrome de) --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=Martin-Bell (syndrome de) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  328. Sydenham (chorée de) --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=Sydenham (chorée de) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  329. Syndrome de De Barsy --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=Syndrome de De Barsy | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  330. Syndrome de Prader-Willi --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=Syndrome de Prader-Willi | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  331. Trisomie --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=Trisomie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  332. arriération --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=arriération | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  333. chorde --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=chorde | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  334. chorde dorsale --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=chorde dorsale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  335. chordome --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=chordome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  336. chordomésoblaste --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=chordomésoblaste | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  337. chorio-amniotite --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=chorio-amniotite | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  338. chorio-angiome --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=chorio-angiome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  339. chorio-épithéliome --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=chorio-épithéliome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  340. choriocapillaire --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=choriocapillaire | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  341. choriocarcinome germinal tératomateux du médiastin --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=choriocarcinome germinal tératomateux du médiastin | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  342. choriocarcinome placentaire --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=choriocarcinome placentaire | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  343. choriocarcinome primitif du col utérin --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=choriocarcinome primitif du col utérin | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  344. choriogonadotrophine --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=choriogonadotrophine | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  345. chorioméningite lymphocytaire --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=chorioméningite lymphocytaire | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  346. danse de Saint Guy --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=danse de Saint Guy | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  347. de Barsy (syndrome de) --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=de Barsy (syndrome de) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  348. en:Cayler cardiofacial syndrome --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:Cayler cardiofacial syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  349. en:Chopart's amputation --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:Chopart's amputation | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  350. en:Down's --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:Down's | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  351. en:Down's syndrome --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:Down's syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  352. en:Fryns syndrome --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:Fryns syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  353. en:Huntington's chorea --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:Huntington's chorea | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  354. en:PWS --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:PWS | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  355. en:cacomorphosis --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:cacomorphosis | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  356. en:contractural arachnodactyly --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:contractural arachnodactyly | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  357. en:cyclops eye --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:cyclops eye | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  358. en:de Barsy?s syndrome --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:de Barsy?s syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  359. en:de Sanctis-Cacchione syndrome --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:de Sanctis-Cacchione syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  360. en:executive functions --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:executive functions | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  361. en:hypoacousic child --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:hypoacousic child | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  362. en:infantile finnish type --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:infantile finnish type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  363. en:trisomy 21 --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:trisomy 21 | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  364. en:van der Woude syndrome --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=en:van der Woude syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  365. encéphalocèle --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=encéphalocèle | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  366. goniome --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=goniome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  367. goniomètre --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=goniomètre | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  368. gonion --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=gonion | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  369. gonioscopie --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=gonioscopie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  370. goniosynéchies --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=goniosynéchies | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  371. goniotomie endoscopique --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=goniotomie endoscopique | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  372. gonochorisme --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=gonochorisme | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  373. gonococcie --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=gonococcie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  374. gonocoque --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=gonocoque | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  375. gonocyte --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=gonocyte | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  376. gonocytome --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=gonocytome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  377. gonométrie --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=gonométrie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  378. gonorrhée --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=gonorrhée | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  379. gonosome --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=gonosome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  380. gonosomique --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=gonosomique | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  381. maladie de Gaucher --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=maladie de Gaucher | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  382. nystagmus héréditaire vertical --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=nystagmus héréditaire vertical | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  383. nystagmus lié au sexe --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=nystagmus lié au sexe | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  384. nystagmus myoclonies --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=nystagmus myoclonies | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  385. sirtuine --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=sirtuine | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  386. sisi-test --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=sisi-test | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  387. sismothérapie --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=sismothérapie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  388. triphosphopyridine-nucléotide --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=triphosphopyridine-nucléotide | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  389. trisomie 9p --- r_associated #0: 10 --> en:harrod doman keele syndrome
    n1=trisomie 9p | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=10
  390. chorial, ale --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=chorial, ale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  391. chorio-adénome destruens --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=chorio-adénome destruens | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  392. chorée fibrillaire de Morvan --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=chorée fibrillaire de Morvan | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  393. chorée gravidique --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=chorée gravidique | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  394. choréo-acanthocytose --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=choréo-acanthocytose | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  395. cyclopeptide --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=cyclopeptide | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  396. cyclophiline --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=cyclophiline | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  397. cyclophorie --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=cyclophorie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  398. cyclophosphamide --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=cyclophosphamide | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  399. cyclophotocoagulation endoscopique --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=cyclophotocoagulation endoscopique | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  400. cyclophrénie --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=cyclophrénie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  401. cyclophyllidés --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=cyclophyllidés | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  402. exencéphale --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=exencéphale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  403. exénatide --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=exénatide | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  404. faisceau de His --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=faisceau de His | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  405. histaminergie --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=histaminergie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  406. histaminergique --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=histaminergique | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  407. histaminique --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=histaminique | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  408. histaminolibération --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=histaminolibération | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  409. histaminolytique --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=histaminolytique | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  410. histaminopexie --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=histaminopexie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  411. histaminurie --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=histaminurie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  412. histaminémie --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=histaminémie | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  413. histidase --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=histidase | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  414. histidinase --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=histidinase | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  415. histidine --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=histidine | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  416. histidine-ammoniac-lyase --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=histidine-ammoniac-lyase | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  417. histidine-décarboxylase --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=histidine-décarboxylase | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  418. histidine-désaminase --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=histidine-désaminase | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  419. malf ormation dysraphique --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=malf ormation dysraphique | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  420. malformation kystique adénomatoïde du poumon --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=malformation kystique adénomatoïde du poumon | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  421. malformation luxante de la hanche --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=malformation luxante de la hanche | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  422. malformation mamelonnaire --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=malformation mamelonnaire | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  423. malformation mammaire --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=malformation mammaire | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  424. malformation ombilicale --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=malformation ombilicale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  425. malformation utérine --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=malformation utérine | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  426. malformation vaginale --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=malformation vaginale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  427. malformation vasculaire cérébrale du nourrisson --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=malformation vasculaire cérébrale du nourrisson | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  428. malformations de la charnière occipitocervicale --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=malformations de la charnière occipitocervicale | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  429. nystagmus (zone de moindre) --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=nystagmus (zone de moindre) | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  430. triplet (CGG) n --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=triplet (CGG) n | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  431. trisomie 13 --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=trisomie 13 | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  432. trisomie 17p11.2 --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=trisomie 17p11.2 | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  433. trisomie 18 --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=trisomie 18 | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
  434. trisomie 8 --- r_associated #0: 5 --> en:harrod doman keele syndrome
    n1=trisomie 8 | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=5
Le service Rézo permet d'énumérer les relations existant pour un terme. Ce service est interrogeable par programme.
Projet JeuxDeMots - url: http://www.jeuxdemots.org
contact: mathieu.lafourcade@lirmm.fr